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Sample records for resin dowex 50w-x8

  1. Distribution ratios on Dowex 50W resins of metal leached in the caron nickel recovery process

    Energy Technology Data Exchange (ETDEWEB)

    Reynolds, B.A.; Metsa, J.C.; Mullins, M.E.

    1980-05-01

    Pressurized ion exchange on Dowex 50W-X8 and 50W-X12 resins was investigated using elution techniques to determine distribution ratios for copper, nickel, and cobalt complexes contained in ammonium carbonate solution, a mixture which approximates the waste liquor from the Caron nickel recovery process. Results were determined for different feed concentrations, as well as for different concentrations and pH values of the ammonium carbonate eluant. Distribution ratios were compared with those previously obtained from a continuous annular chromatographic system. Separation of copper and nickel was not conclusively observed at any of the conditions examined.

  2. Distribution ratios on Dowex 50W resins of metal leached in the caron nickel recovery process

    International Nuclear Information System (INIS)

    Reynolds, B.A.; Metsa, J.C.; Mullins, M.E.

    1980-05-01

    Pressurized ion exchange on Dowex 50W-X8 and 50W-X12 resins was investigated using elution techniques to determine distribution ratios for copper, nickel, and cobalt complexes contained in ammonium carbonate solution, a mixture which approximates the waste liquor from the Caron nickel recovery process. Results were determined for different feed concentrations, as well as for different concentrations and pH values of the ammonium carbonate eluant. Distribution ratios were compared with those previously obtained from a continuous annular chromatographic system. Separation of copper and nickel was not conclusively observed at any of the conditions examined

  3. Alkali metal ion-proton exchange equilibria and water sorption studies on nafon 117 membrane and dowex 50 W exchange resins: effect of long storage or aging

    International Nuclear Information System (INIS)

    Ramkumar, Jayshree; Venkataramani, B.

    2004-09-01

    Alkali metal ion -H + exchanges on Nafion 117 membrane treated differently, Dowex 50 W x 4 and Dowex 50 W x 8 resins have been studied at a total ionic strength of 0.1 mol dm -3 . The water sorption isotherms of these exchangers in different ionic forms generated over the entire range of water activity, have been analysed by the D'Arcy and Watt equation (DWE). Water sorption studies have shown that the physical structure of the exchangers have changed due to long -storage or aging, resulting in poorer water sorption and even formation of pores in the case of Dowex 50 W x 8 resin. As a result, the counter ions in the exchangers are not hydrated and the water is present in a free form, albeit structured, in the resin phase. The selectivity sequence for the alkali metal ions with reference to the H + (Li + + + ) for the exchangers used in the present study is in accordance with that reported in the literature for the ionomers having sulphonic acid as the functional group. In view of the absence of hydration of the cations in the resin phase, the driving force for the selectivity of the cation, namely, the net gain in entropy, is expected to come from the loss of structured water during the exchange process. Pre treating the Nafion 117 membrane with boiling acid solution activates the clustered region of the membrane in the H + form, while pretreatment with boiling water expands the non-ionic domain (the region connecting the clusters). These modifications influence the state of water present in the Nafion 117 membrane and the ion exchange equilibria. As a result of long storage or aging, the ion exchangers lose their elasticity or swelling characteristics. The results obtained in the present study indicate that in aged materials, the ionogenic groups are existing as isolated ion -pairs rather than in a clustered morphology. (author)

  4. Radiation effects on ion-exchange resins. Part II. Gamma irradiation of Dowex 1

    International Nuclear Information System (INIS)

    Kazanjian, A.R.; Horrell, D.R.

    1975-01-01

    The effects were determined of gamma radiation on the anion exchange resin, Dowex 1. Part I on Dowex 50W was reported May 10, 1974. The exchange capacity (both strong and weak base), moisture content, radiolysis products, and physical deterioration of the resin were analyzed after irradiation with doses up to 6.9 x 10 8 rads. The resin capacity decreased approximately 50 percent after a radiation dose of 4 x 10 8 rads. Resin irradiated, when air dried in the nitrate form, showed more stability than resin irradiated in 7N nitric acid (HNO 3 ), which in turn showed more stability than resin irradiated when air dried in the chloride form. Radiation decreased the strong base capacity to a greater extent than the total capacity. The result indicates that some of the quarternary ammonium groups were transformed to secondary and tertiary amine groups that have weak base ion-exchange capability. (U.S.)

  5. Studies on the adsorption behaviour of heavy rare earths with a strong cation exchanger DOWEX 50W-2X8

    International Nuclear Information System (INIS)

    Vijayalakshmi, R.; Singh, D.K.; Anitha, M.; Kotekar, M.K.; Dasgupta, K.; Singh, H.

    2014-01-01

    Rare earths have been a very fascinating area of research since long due to its wide applicability's in many field including superconductors, lasers, phosphors, medical, electronics, magnet, optics etc. Separation of rare earths is a challenging task and over the years many separation schemes based on solvent extraction, ion exchange, membrane etc have been developed and deployed. In the present work, we have investigated the adsorption behavior of heavy rare earths from a crude concentrate analyzing ∼ 80% Y 2 O 3 , ∼12% Dy 2 O 3 , ∼4% Er 2 O 3 etc., with a strong cationic exchanger namely Dowex 50W-2X8 in order to separate them in pure form. To start with, Y was selected as a representative of heavy rare earths and the conditions were optimized in batch experiments and later were applied to the feed solution containing Dy, Er, Ho etc. in a column study. Effects of experimental variables such as contact time, pH, weight of resin, concentration of the feed metal, temperature, desorption agents, on adsorption of Y was studied

  6. Molybdenum adsorption by alumina and Dowex 1x8 resin for the separation and purification process of fission 99Mo

    International Nuclear Information System (INIS)

    Yamaura, M.; Damasceno, M.O.; Freitas, A.A.; Camilo, R.L.; Araujo, I.C.; Forbicini, C.A.L.G. de O.

    2011-01-01

    Molybdenum-99 is the most widely employed radioisotope in nuclear medicine, due to its decay product, Technetium-99m, a radioisotope used in over 80% of diagnostic tests. Since 2009, the production of generators 99 Mo/ 99m Tc suffers a crisis of global supply. The raw material, the 99 Mo, is produced mainly by fission of 235 U in the reactor in uranium targets. Brazilian government invests in building of a research reactor suitable for the domestic production of 99 Mo from LEU (Low Enriched Uranium) targets and the IPEN/CNEN develops the production technology. This work is part of the research for the development of production technology of 99 Mo at the IPEN/CNEN-SP. The study has evaluated the adsorption behaviour of molybdenum from the alkaline dissolution of aluminum plates by the alumina and by the anionic resin Dowex 1x8 aiming at their use in the process of separation and purification in chromatography columns. Influences of pH and of aluminum concentration in the retention of molybdenum were investigated. Results showed high performance in the wide pH range. However in strongly acid solutions containing aluminum, alumina showed higher adsorption percentage than that achieved by the resin Dowex 1x8. (author)

  7. Molybdenum adsorption by alumina and Dowex 1x8 resin for the separation and purification process of fission {sup 99}Mo

    Energy Technology Data Exchange (ETDEWEB)

    Yamaura, M.; Damasceno, M.O.; Freitas, A.A.; Camilo, R.L.; Araujo, I.C.; Forbicini, C.A.L.G. de O., E-mail: myamaura@ipen.b, E-mail: molidam@ipen.b, E-mail: afreitas@ipen.b, E-mail: rcamilo@ipen.b, E-mail: cruz.araujo@uol.com.b, E-mail: cforbici@ipen.b [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2011-07-01

    Molybdenum-99 is the most widely employed radioisotope in nuclear medicine, due to its decay product, Technetium-99m, a radioisotope used in over 80% of diagnostic tests. Since 2009, the production of generators {sup 99}Mo/{sup 99m}Tc suffers a crisis of global supply. The raw material, the {sup 99}Mo, is produced mainly by fission of {sup 235}U in the reactor in uranium targets. Brazilian government invests in building of a research reactor suitable for the domestic production of {sup 99}Mo from LEU (Low Enriched Uranium) targets and the IPEN/CNEN develops the production technology. This work is part of the research for the development of production technology of {sup 99}Mo at the IPEN/CNEN-SP. The study has evaluated the adsorption behaviour of molybdenum from the alkaline dissolution of aluminum plates by the alumina and by the anionic resin Dowex 1x8 aiming at their use in the process of separation and purification in chromatography columns. Influences of pH and of aluminum concentration in the retention of molybdenum were investigated. Results showed high performance in the wide pH range. However in strongly acid solutions containing aluminum, alumina showed higher adsorption percentage than that achieved by the resin Dowex 1x8. (author)

  8. Studies on molybdenum elution study in dowex 1x8 resin applied on purification process of fission 99Mo

    International Nuclear Information System (INIS)

    Damasceno, M.O.; Yamaura, M.; Santos, J.L. dos; Forbicini, C.A.L.G. de O.

    2013-01-01

    Molybdenum-99 is the most widely employed radioisotope in nuclear medicine, due to its decay product, Technetium-99, which is used in radio-pharmaceutical marking molecules for diagnostic examinations tumor dis-eases. Today Brazil imports 99 Mo from some countries, so the National Commission of Nuclear Energy (CNEN) is implementing a new research reactor RMB, currently in the conceptual design phase. The process of separation of fission 99 Mo begins with the dissolution of uranium targets after irradiation in reactor; the resulting solution goes through a series of chromatographic columns that allows a gradual decontamination of other components, yielding the 99 Mo with high radio-chemical and chemical purity for use in nuclear medicine as a generator of 99 mTc. This work is part of the RMB research project to separate and purify the fission 99 Mo by chromatographic columns from alkaline dissolution of LEU UAl x -Al targets. In the present study Mo removal by batch assays and glass column was investigated using anionic exchanger Dowex 1x8. Different salts and its concentration, cations and temperature were evaluated on elution of molybdenum and iodine (contaminant) retained on resin Dowex 1x8, aiming at their use in the process of separation and purification in chromatography columns on Brazilian project. Results showed high recovery of Mo and low-level contamination by iodine using NaHCO 3 hot solution. (author)

  9. Method for immobilizing invertase by adsorption on Dowex® anionic exchange resin Método para a imobilização da invertase por adsorção em resinas trocadoras de ânions (DOWEX

    Directory of Open Access Journals (Sweden)

    Ester Junko Tomotani

    2006-06-01

    Full Text Available This communication describes a method for adsorbing the invertase (EC.3.2.1.26 on DOWEX® anion exchange resin. Among the types of DOWEX® resins studied (1x8:50-400; 1x4:50-400 and 1x2:100-400, 1X4-200 was the most suitable, because it adsorbed the invertase molecules completely and the complex 1X4-200/invertase retained 100% of the catalytic activity. Moreover, no leakage of enzyme from the support was noted at the end of the sucrose hydrolysis.O presente trabalho descreve um método de adsorção da invertase (EC. 3.2.1.26 na resina de troca aniônica do tipo Dowex®. Entre os tipos de resinas Dowex® estudados (1x8:50-400; 1x4:50-400 e 1x2:100-400, 1x4-200 foi a mais apropriada devido à completa adsorção das moléculas de invertase e a sua retenção de atividade catalítica de 100% do complexo 1x4-200/invertase. Salienta-se ainda a ausência do desprendimento da enzima do suporte após o término da hidrólise da sacarose.

  10. Comparative study of the ionic exchange of Ca{sup ++}, Sr{sup ++}, and Ba{sup ++} cations on resins and inorganic exchangers; Etude comparative de l'echange ionique des cations Ca{sup ++}, Sr{sup ++} et Ba{sup ++} sur resine et sur echangeurs mineraux

    Energy Technology Data Exchange (ETDEWEB)

    Sanchez Batanero, P [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1969-03-01

    With a view to applying the results to certain problems related to chemical separations in activation analysis, a study has been made, of the possibilities of separating the alkaline-earth elements Ca, Sr and Ba on organic resins and inorganic exchangers using the radioactive indicator method. The partition coefficients of the cations Ca{sup 2+}, Sr{sup 2+} and Ba{sup 2+} have been measured on Dowex 50 W (NH{sub 4}{sup +}) x 8 resin in the presence of EDTA - NTA - EGTA and DCTA as complexing agents, and on zirconium phosphate, tungstate and molybdate in the presence of HCl and NH{sub 4}Cl. Methods have been developed for separating mixtures of alkaline-earth elements using DCTA-NH{sub 4}{sup +} followed by elution on Dowex 50 W (NH{sub 4}{sup +}) x 8 resin columns and on zirconium phosphate. Amongst the complexing agents used on the ion-exchange resins the most promising appears to be DCTA which leads to partition coefficients Ca, Sr and Ba which are very different. The results of measurements of partition coefficients on zirconium phosphate (NH{sub 4}{sup +} form) using DCTA-NH{sub 4}{sup +} show the interesting possibilities of separations on columns. The separation of the alkaline-earth elements on zirconium phosphate seems to be less quantitative than on Dowex 50 resin; it is however much faster in the former case and this can be useful for treating short half-life radioisotopes in activation analysis. (author) [French] En vue de l'application a certains problemes de separations chimiques en analyse par activation, on a etudie les possibilites de separation des elements alcalino-terreux Ca-Sr et Ba sur resine organique et sur echangeurs mineraux par la methode des indicateurs radioactifs. Les coefficients de partage des cations Ca{sup +2}, Sr{sup +2} et Ba{sup +2} sur resine Dowex 50 W (NH{sub 4}{sup +}) x 8 en milieux complexants EDTA - NTA - EGTA et DCTA et sur phosphate, tungstate et molybdate de zirconium en milieu HCl et NH{sub 4}Cl ont ete mesures. Des

  11. Comparative study of the ionic exchange of Ca++, Sr++, and Ba++ cations on resins and inorganic exchangers

    International Nuclear Information System (INIS)

    Sanchez Batanero, P.

    1969-03-01

    With a view to applying the results to certain problems related to chemical separations in activation analysis, a study has been made, of the possibilities of separating the alkaline-earth elements Ca, Sr and Ba on organic resins and inorganic exchangers using the radioactive indicator method. The partition coefficients of the cations Ca 2+ , Sr 2+ and Ba 2+ have been measured on Dowex 50 W (NH 4 + ) x 8 resin in the presence of EDTA - NTA - EGTA and DCTA as complexing agents, and on zirconium phosphate, tungstate and molybdate in the presence of HCl and NH 4 Cl. Methods have been developed for separating mixtures of alkaline-earth elements using DCTA-NH 4 + followed by elution on Dowex 50 W (NH 4 + ) x 8 resin columns and on zirconium phosphate. Amongst the complexing agents used on the ion-exchange resins the most promising appears to be DCTA which leads to partition coefficients Ca, Sr and Ba which are very different. The results of measurements of partition coefficients on zirconium phosphate (NH 4 + form) using DCTA-NH 4 + show the interesting possibilities of separations on columns. The separation of the alkaline-earth elements on zirconium phosphate seems to be less quantitative than on Dowex 50 resin; it is however much faster in the former case and this can be useful for treating short half-life radioisotopes in activation analysis. (author) [fr

  12. Flow-injection determination of thorium and uranium after on-line ion-exchange preconcentration in Dowex 50-X8

    International Nuclear Information System (INIS)

    Perez Pavon, J.L.; Garcia Pinto, C.G.; Rodriguez Garcia, Estrella; Moreno Cordero, Bernardo

    1992-01-01

    The preconcentration of thorium and uranium on Dowex 50-X8 was studied as a method for the preconcentration of these cations prior to their determination by flow injection with spectrophotometric detection using Arsenazo III in 3.6 M HCl stabilized with Triton X-100 as chromogenic reagent. The preconcentration device is a minicolumn included in the sample loop of the injection valve. A second valve contains a reducing minicolumn filled with lead powder to reduce U(VI) to U(IV) before the confluence of the sample with the reagent stream. The method can be applied to samples containing 0.5-100 μg l -1 and was tested with different spiked water samples. (author). 15 refs.; 3 figs.; 3 tabs

  13. The determination of iodine in cheese by neutron activation combined with separation of iodine by selective retention on Dowex 2-X8

    International Nuclear Information System (INIS)

    Nordbye, P.I.; Augustson, J.H.

    1980-03-01

    Iodine has been determined in Norwegian cheese by combination of neutron activation and subsequent separation of radioiodine ( 128 I) by selective retention on Dowex 2-X8 anion exchange resin. Iodine may be detected down to 5ng in terms of absolute amounts. In terms of concentration the detection limit was 10ppb. Results showed a precision of 5 percent at a concentration level of 1ppm. (Auth.)

  14. Determination of γ-Aminobutyric Acid (GABA) in Rambutan Fruit cv. Rongrian by HPLC-ELSD and Separation of GABA from Rambutan Fruit Using Dowex 50W-X8 Column.

    Science.gov (United States)

    Meeploy, Maneerat; Deewatthanawong, Rujira

    2016-03-01

    A high-performance liquid chromatography method coupled with an evaporative light scattering detector (ELSD) was validated for the determination of γ-aminobutyric acid (GABA) in rambutan fruit without any sample pretreatment or derivatization. In the concentration range of 0.05-1.0 mg/mL GABA, the ELSD response was linear with a correlation coefficient (r) >0.999. Limit of detection and limit of quantitation were found to be 0.7 and 2.0 µg/mL, respectively. The method enabled the complete separation of GABA in the aqueous extract of rambutan flesh from the impurity peaks at 45.7 min. The recoveries of sample added GABA were obtained in the range of 92.0-99.3%. Intraday and interday relative standard deviations were rambutan flesh, 0.71 ± 0.23 mg of GABA was found in 1 g fresh weight. The recovery of GABA after passing through the Dowex 50W-X8 column was 96.65%. The analytical methodology could be potentially applied to the detection and quantification of GABA in other fruits and complex matrices when a sufficient quantity is available. © The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

  15. Recovery of tretrachloroaurate through ion exchange with Dowex 11 resin

    International Nuclear Information System (INIS)

    Alguacil, F.J.

    1998-01-01

    The recovery of the tretrachloroaurate complex by the anionic ion exchange resin Dowex 11 has been studied. The kinetics of gold adsorption were dependent of both gold and resin concentrations and temperature. The adsorption isotherm can be described by the expression Q=kC''n. The loaded resin could be eluted by an acidic thiourea solution at 20 degree centigree. After several adsorption-elution cycles there is not any apparent loss in the adsorption properties of the resin. (Author) 6 refs

  16. Ion-Isotopic Exchange Reaction Kinetics using Anion Exchange Resins Dowex 550A LC and Indion-930A

    Directory of Open Access Journals (Sweden)

    P.U. Singare

    2014-06-01

    Full Text Available The present paper deals with the characterization of ion exchange resins Dowex 550A LC and Indion-930A based on kinetics of ion-isotopic exchange reactions for which the short lived radioactive isotopes 131I and 82Br were used as a tracers. The study was performed for different concentration of ionic solution varying from 0.001 mol/L to 0.004 mol/L and temperature in the range of 30.0 °C to 45.0 °C. The results indicate that as compared to bromide ion-isotopic exchange reaction, iodide exchange reaction take place at the faster rate. For both the ion-isotopic exchange reactions, under identical experimental conditions, the values of specific reaction rate increases with increase in the ionic concentration and decreases with rise in temperature. It was observed that at 35.00C, 1.000 g of ion exchange resins and 0.002 mol/L labeled iodide ion solution for iodide ion-isotopic exchange reaction, the values of specific reaction rate (min-1, amount of ion exchanged (mmol, initial rate of ion exchange (mmol/min and log Kd were 0.270, 0.342, 0.092 and 11.8 respectively for Dowex 550A LC resin, which was higher than the respective values of 0.156, 0.241, 0.038 and 7.4 as that obtained for Indion-930A resins. From the results, it appears that Dowex 550A LC resins show superior performance over Indion-930A resins under identical experimental conditions.

  17. Radiotracer application for characterization of nuclear grade anion exchange resins Tulsion A-23 and Dowex SBR LC

    International Nuclear Information System (INIS)

    Singare, P.U.

    2015-01-01

    Radio isotopic tracer technique as one of the versatile nondestructive technique is employed to evaluate the performance of nuclear grade anion exchange resins Tulsion A-23 and Dowex SBR LC. The evaluation was made on the basis of ion-isotopic exchange reaction kinetics by using 131 I and 82 Br radioactive tracer isotopes. It was observed that for both the resins, the values of specific reaction rate (min -1 ), amount of ion exchanged (mmol) and initial rate of ion exchange (mmol/min) were calculated to be lower for bromide ion-isotopic exchange reaction than that for iodide ion-isotopic exchange reaction. It was observed that for iodide ion-isotopic exchange reaction under identical experimental conditions of 30.0 C, 1.000 g of ion exchange resins and 0.001 mol/L labeled iodide ion solution, the values of specific reaction rate (min -1 ), amount of iodide ion exchanged (mmol), initial rate of iodide ion exchange (mmol/min) and log K d were calculated as 0.377, 0.212, 0.080 and 15.5 respectively for Dowex SBR LC resin, which was higher than 0.215, 0.144, 0.031 and 14.1 respectively as that obtained for Tulsion A23 resins. Also at a constant temperature of 30.0 C, as the concentration of labeled iodide ion solution increases from 0.001 mol/L to 0.004 mol/L, the percentage of iodide ions exchanged increases from 84.75 % to 90.20 % for Dowex SBR LC resins which was higher than increases from 57.66 % to 62.38 % obtained for Tulsion A23 resins. The identical trend was observed for the two resins during bromide ion-isotopic exchange reaction. The overall results indicate superior performance of Dowex SBR LC over Tulsion A23 resins under identical experimental conditions.

  18. Studies on the rates of exchange of Hg(II), Cd(II), La(III) and Ce(III) ions in sodium nitrite-aqueous acetone media using an anion-exchanger Dowex-1x8(NO3-)

    International Nuclear Information System (INIS)

    Bhatnagar, R.P.; Bhardwaj, Archana; Bhardwaj, S.D.

    1998-01-01

    Rate of exchange has been studied on Hg(II), Cd(II), La(III) and Ce(III) ions in sodium nitrite-aqueous acetone media using an anion exchanger Dowex-1 x 8(NO 3 - ). Acetone was used to provide solvent media of 10%, 30% and 50% and temperature was used in rate studies, carried out at 30 deg, 40 deg, 50 degC. Always 1 g. of Dowex-1x8 in nitrate form was used for distribution studies to get rate data. After suitable time intervals aliquots (1 ml) were withdrawn and metal ion concentration was found out. (author)

  19. Behaviour of Pu-IV with various ion exchangers in solutions containing nitric acid and oxalates

    International Nuclear Information System (INIS)

    Walter, E.; Ali, S.A.

    1982-02-01

    The distribution of Pu-IV on the ion exchangers Dowex 50W-X8, Dowex 1-X8 und Dowex Chelating Resin Al-X8 in the presence of various concentrations of nitric acid and oxalate were investigated. The results indicate that nitric acid and oxalic acid influence each other during complexation of Pu-IV with oxalate ions solutions containing nitric acid it is not possible to neglect the formation of Pu-IV nitrate complexes. The complex Pu(IV) (C 2 O 4 ) 3 2 - only is formed in solutions containing low nitric acid and high oxalic acid concentrations. The separation of Pu-IV in Dowex Chelating Resin from nitric acid solution in the presence of higher oxalate concentrations is possible, provided that the nitric acid concentration is lower than 0.25 molar [fr

  20. Dissolution of ion exchange resin by hydrogen peroxide

    International Nuclear Information System (INIS)

    Lee, S.C.

    1981-08-01

    The resin dissolution process was conducted successfully in full-scale equipment at the SRL Semiworks. A solution containing 0.001M Fe 2+ , or Fe 3+ , and 3 vol % H 2 O 2 in 0.1M HNO 3 is sufficient to dissolve up to 40 vol % resin slurry (Dowex 50W-X8). Foaming and pressurization can be eliminated by maintaining the dissolution temperature below 99 0 C. The recommended dissolution temperature range is 85 to 90 0 C. Premixing hydrogen peroxide with all reactants will not create a safety hazard, but operating with a continual feed of hydrogen peroxide is recommended to control the dissolution rate. An air sparging rate of 1.0 to 1.5 scfm will provide sufficient mixing. Spent resin from chemical separation contains DTPA (diethylenetriaminepentaacetic acid) residue, and the resin must be washed with 0.1M NH 4 OH to remove excess DTPA before dissolution. Gamma irradiation of resin up to 4 kW-hr/L did not change the dissolution rate significantly

  1. The removal of toxic metals from liquid effluents by ion exchange resins. Part V: Nickel(II/H+/Dowex C400

    Directory of Open Access Journals (Sweden)

    Francisco José Alguacil

    2017-11-01

    Full Text Available The cationic exchange resin Dowex C400 was used to remove nickel(II from aqueous solutions of different pH values and under various experimental conditions: stirring speed of the aqueous solution/resin system, temperature, resin dosage and aqueous ionic strength. The selectivity of the resin was investigated against the presence of various metals in the aqueous solution, and the removal of nickel(II from aqueous solutions was also compared with results obtained using multiwalled carbon nanotubes or functionalized (carboxylic groups multiwalled carbon nanotubes as adsorbents. According to batch experimental data, best fit of the results is obtained with the Freundlich model, whereas the ion exchange process is best explained by the pseudo-first order model. Experimental data fit well to the moving boundary controlled model. Elution of the nickel(II loaded onto Dowex C400 resin is fully possible using acidic solutions.

  2. Kinetics of ion exchange in the chelating resin Dowex A-1

    International Nuclear Information System (INIS)

    Matsuzuru, Hideo; Wadachi, Yoshiki

    1975-01-01

    The kinetics of ion exchanges of Ag + , Zn 2+ and Cr 3+ at extremely low concentrations on the chelating resin Dowex A-1 has been studied by means of finite volume method. The rate of exchanges for both Ag + and Zn 2+ is dependent on the ionic strength, particle size of the resin and reaction temperature. At higher ionic strength (0.1 - 0.05) the kinetics is controlled by particle diffusion, whereas at lower ionic one (0.01 - 0.001) film diffusion is predominant. The apparent activation energy obtained is 3.84 kcal/mol for Ag + and 3.91 kcal/mol for Zn 2+ . The exchange rate of Cr 3+ obeys a first-order rate equation independent of the ionic strength and particle size of the resin. The apparent activation energy is 15.5 kcal/mol. These results support the view that the rate-determining step of this reaction is chelate formation reaction. (auth.)

  3. Possibilities of chemical isolation of element 106 from aqueous solutions according to the model experiments with short lived tungsten isotopes

    International Nuclear Information System (INIS)

    Szeglowski, Z.; Bruchertseifer, H.; Brudanin, V.B.

    1993-01-01

    A rapid method for continuous separation of short-lived tungsten isotopes from the lanthanides has been developed. It consists in transforming nuclear reaction products from the target by an aerosol jet to an absorber where the KCl particulates are dissolved in 0.2 M HF and percolating the product solution through three successively linked columns filled with ion exchange resins Dowex 50X8 (cationite), Dowex 1X8 (anionite) and again Dowex 50X8. 3 refs

  4. An efficient ultrasound assisted approach for the impregnation of room temperature ionic liquid onto Dowex 1 × 8 resin matrix and its application toward the enhanced adsorption of chromium (VI)

    International Nuclear Information System (INIS)

    Kalidhasan, S.; Santhana Krishna Kumar, A.; Vidya Rajesh; Rajesh, N.

    2012-01-01

    Highlights: ► Ultrasound assisted impregnation of an ionic liquid in a Dowex resin matrix is studied through various physicochemical and spectroscopic techniques. ► Chromium is adsorbed with a high adsorption capacity of 230.9 mg g −1 . ► The adsorbent is regenerated using HCl–ascorbic acid mixture. ► Chromium could be effectively detoxified from an industrial effluent and the developed method was validated with the analysis of a certified reference material. - Abstract: The work discussed in this paper is based on the utilization of ultrasound in conjunction with an ionic liquid (Aliquat 336) impregnated Dowex 1 × 8 resin for the effective adsorption of chromium. Ionic liquids are known for their selectivity toward metal extraction and ultrasonic medium offers efficient energy transfer for impregnating the ionic liquid in the resin matrix. The molecular interaction between the ionic liquid impregnated resin and chromium was studied through various physicochemical and spectroscopic techniques. The influence of various analytical parameters on the adsorption of Cr(VI) such as pH, adsorbent dosage, temperature and interference of foreign ions was studied in detail. Chromium (VI) was quantitatively adsorbed in the pH range of 3.5–4, with a high adsorption capacity of 230.9 mg g −1 in conformity with the Langmuir isotherm model. The study of thermodynamic parameters showed that the adsorption process is exothermic and spontaneous. The adsorbent could be regenerated using 1 mol L −1 HCl–0.28 mol L −1 ascorbic acid mixture. Chromium could be effectively detoxified from an industrial effluent and finally the developed method was validated with the analysis of a certified reference material (BCR-715). The obtained results indicated that the ultrasonic assisted impregnation of the room temperature ionic liquid significantly enhances and improves the removal efficiency of Cr(VI).

  5. Basic Retention Mechanisms

    DEFF Research Database (Denmark)

    Jensen, Bror Skytte; Jensen, H.

    1986-01-01

    The effect of multiple cation competition on the adsorption of Sr onto two synthetic ion-exchange resins, i. e. DOWEX 50W and DOWEX CCR-2, as well as onto the clay mineral, kaolinite has been studied. The results for DOWEX 50W, and under certain experimental conditions also for DOWEX CCR-2 were...

  6. Esterification of free fatty acids in waste cooking oils (WCO): Role of ion-exchange resins

    Energy Technology Data Exchange (ETDEWEB)

    Nalan Ozbay; Nuray Oktar; N. Alper Tapan [Gazi University, Ankara (Turkey). Faculty of Engineering and Architecture, Department of Chemical Engineering

    2008-08-15

    Although WCO plays a crucial role for the economical production of biodiesel, free fatty acid (FFA) level in the nature of WCO cause saponification problems during transesterification. Acidic ion-exchange resins can be used to decrease WCO free fatty acid level. In this study, activities of resins (Amberlyst-15 (A-15), Amberlyst-35 (A-35), Amberlyst-16 (A-16) and Dowex HCR-W2) in direct FFA esterification were examined in the temperature range of 50-60{sup o}C and the effect of catalyst amount (1-2 wt%) on FFA conversion was also analyzed. FFA conversion increased with increasing reaction temperature and catalyst amount. Order of catalytic activities was found as A-15 > A-35 > A-16 > Dowex HCR-W2. This was related to the size of average pore diameters and magnitude of BET surface area. 44 refs., 11 figs., 2 tabs.

  7. The absorption of plutonium by anion resins

    Energy Technology Data Exchange (ETDEWEB)

    Durham, R. W.; Mills, R.

    1961-10-15

    Equilibrium experiments have shown Pu{sup +4} to be absorbed from nitric acid onto an anion resin as a complex anion Pu(NO{sub 3}){sub 6}{sup -2}. The amount of absorption is dependent on the plutonium and nitric acid concentrations in the equilibrium solution with a maximum at 7N to 8N HNO{sub 3}. A low cross-linked resin has a higher capacity and reaches equilibrium more rapidly than the normally supplied resin. Saturation capacity of one per cent cross-linked Nalcite SBR (Dowex 1), 50 -- 100 mesh, is 385 mg Pu/gram dry resin. (author)

  8. Separation of zirconium from hafnium by ion exchange

    Energy Technology Data Exchange (ETDEWEB)

    Felipe, Elaine C.B.; Palhares, Hugo G.; Ladeira, Ana Claudia Q., E-mail: elainecfelipe@yahoo.com.br, E-mail: hugopalhares@gmail.com, E-mail: ana.ladeira@cdtn.br [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil)

    2013-07-01

    Zirconium and hafnium are two of the most important metals for the nuclear industry. Hafnium occurs in all zirconium ores usually in the range 2 - 3%. However, for the most nuclear industry applications, it is necessary to use a zirconium of extremely pure level. The current work consists in the separation of zirconium and hafnium by the ion exchange method in order to obtain a zirconium concentrate of high purity. The zirconium and hafnium liquors were produced from the leaching of the Zr(OH){sub 4} and Hf(OH){sub 4} with nitric acid for 24 hours. From these two liquors it was prepared one solution containing 7.5 x 10{sup -2} mol L{sup -1} of Zr and 5.8 x 10{sup -3} mol L{sup -1} of Hf with acidity of 1 M. Ion exchange experiments were carried out in batch with the resins Dowex 50WX4, Dowex 50WX8 100, Dowex 50WX8 50, Amberlite IR-120 and Marathon C at constant temperature 28 deg C. Other variables such as, acidity and agitation were kept constant. The data were adjusted to Langmuir equation in order to calculate the maximum loading capacity (q{sub max}) of the resins, the distribution coefficient (K{sub d}) for Zr and Hf and the separation factor (α{sub Hf}{sup Zr} ). The results of maximum loading capacity (q{sub max}) for Zr and Hf, in mmol g{sup -}1, showed that the most suitable resins for columns experiments are: Dowex 50WX4 50 (q{sub max} Z{sub r} = 2.21, Hf = 0.18), Dowex 50WX8 50 (q{sub max} Zr = 1.89, Hf = 0.13) and Amberlite (q{sub max} Zr = 1.64, Hf = 0.12). However, separations factors, α{sub Hf}{sup Zr}, showed that the resins are not selective. (author)

  9. Sorption of plutonium and curium on ion exchange resins in mixed aqueous organic solutions

    International Nuclear Information System (INIS)

    Haidvogel, N.; Reitsamer, G.; Grass, F.

    1974-12-01

    The sorption of the sulfate and nitrate-complexes of the actinides Pu(III), Pu(IV), Pu(VI), Am(III) and Om(III) on the ion-exchange-resins Dowex 1X8 and Dowex 50 WX8 is investigated. The strong sorbability of these actinide ions in solvents with high content of alcohol is explained by the existence of anionic complexes like Pu(III) (SO 4 ) 2 - , Pu(IV) (SO 4 ) 3 2 - , Pu(VI)O 2 (SO 4 ) 2 2 - , Am(SO 4 ) 2 - respectively Am(NO 3 ) 4 - and Om(NO 3 ) 4 - . The taking of autoradiographs from the thin-layer chromatograms by the aid of a special device and the evaluation of the autoradiographs by a particular photodensitometer are described. The measurement of the radioactivity of the α-emitting nuclides Pu 239, Am 241 and Om 242 are done by liquid-scintillation spectrometry. (author)

  10. A comparison study on the use of Dowex 1 and TEVA-resin in determination of 99Tc in environmental and nuclear coolant samples in a SIA system with ICP-MS detection.

    Science.gov (United States)

    Kołacińska, Kamila; Samczyński, Zbigniew; Dudek, Jakub; Bojanowska-Czajka, Anna; Trojanowicz, Marek

    2018-07-01

    This work refers to a comparative study of sorbents widely used in determinations of 99 Tc such as TEVA resin and Dowex 1. Despite having a similar functional group of quaternary amines, both materials represent different chromatographic methods-extraction (TEVA resin) and anion exchange (Dowex 1)-which provides a diverse range of their properties significant in determination of 99 Tc in flow conditions. The comparative tests, carried out in a SIA-LOV (Sequential Injection Analysis-Lab-on-Valve) system combined with mass spectrometric (ICP-MS) detection, considered several factors that are crucial from the standpoint of resin´s utility such as sorption capacity, durability, or selectivity, critical in 99 Tc separation from interferences. The developed and optimized analytical procedure based on the application of the TEVA resin provided determinations of 99 Tc at minimum detectable limit (MDL) 6.00 mBq L -1 in 50 min and has been successfully employed in analyses of samples from nuclear industrial and research units (reactor coolant and sewage) as well as from the river surrounding the nuclear reactor. The method proved to be sufficient for routine analysis of water samples in accordance with EPA standards. The reliability of the method was confirmed in the analysis of the BH standard provided by the NPL for inter-laboratory proficiency tests. The 99 Tc recovery for all real samples was evaluated as 80-100%. Copyright © 2018 Elsevier B.V. All rights reserved.

  11. Separation process of 99Mo from 132Te using thiourea as a complex agent. Application to the separation of 99Mo from fission products

    International Nuclear Information System (INIS)

    Mestnik, S.A.C.; Silva, C.P.G. da

    1986-01-01

    A radiochemical method has been developed to separate 99 Mo from 13 2Te both produced in the fission of 235 U. The method is based on the formation of a cationic complex of tellurium with thiourea in acid medium which is retained on the cationic exchange resin (Dowex 50W-X8, 100-200 mesh) while the molyhdenum does not form such complex and passes through. The experimental results show that the retention of Te-thiourea complex on the resin is (98,3 +- 1,1) %. (Author) [pt

  12. Study of plutonium IV elution from macromolecular anion exchange resin by 0.5 M nitric acid

    International Nuclear Information System (INIS)

    Nadkarni, M.N.; Mayankutty, P.C.; Pillai, N.S.; Shinde, S.S.

    1976-01-01

    Preliminary studies indicated that macroreticular resins possess more or less the same capacities and absorption characteristics for thorium, uranium and plutonium from nitric acid solutions as the conventional resins. Detailed studies were, then, conducted. It was found that Pu(IV) can be loaded on the macroreticular anion exchange resin, Amberlyst A-26 from 7.2 M nitric acid in much the same way as Dowex 1x4. It was also observed that the elution of Pu(IV) from Amberlyst A-26 by 0.5 M nitric acid is much more rapid and quantitative than from Dowex 1x4. (author)

  13. Preferential solvation of single ions in mixed solvents: Part 1. New experimental approach and solvation of monovalent ions in methanol-water and acetonitrile-water mixture. Part 2. Theoretical computation and comparison with experimental data

    International Nuclear Information System (INIS)

    Rege, Aarti C.; Venkataramani, B.; Gupta, A.R.

    1999-06-01

    Preferential solvation of single ion solutions has been studied with Li + , Na + , K + and Ag +- forms of Dowex 50W resins of different cross-linkings in methanol-water and acetonitrile (AN)- water mixtures. The solvent uptake by this alkali metal ionic forms of Dowex 50W resins was studied in an isopiestic set-up using 2,4,6 and 8 m LiCl solutions in 11.0, 20.8, 44.3 and 70.2 % (w/w) methanol-water mixtures and that of Na +- and Ag +- forms using 14.6 to 94.3 % (w/w) AN - water mixtures. The solvent sorbed in the resin phase was extracted by Rayleigh-type distillation and analysed gas chromatographically. The data were analysed by the N s (mole fraction of the organic solvent in the resin phase) vs n t au (total solvent content in the resin phase) plots and separation factor, alpha(ratio of mole fraction of the solvents in the resin and solution phases) or N s vs m (molality in the resin phase) plots. The limiting values of these plots gave the composition of the solvent in the primary solvation shell around the single ion. The compositions of the primary solvation shell around Li + , Na + , and K + in methanol-water mixtures and Na + and Ag + in acetonitrile (AN) - water mixtures have been computed using Franks equation and the approach of Marcus and compared with the experimental results obtained with the above mentioned ionic forms of Dowex 50W resins in different mixed solvents. The experimental results for Li + showed good agreement with the values computed using Franks equation for all methanol-water composition. However, in the case of Na + and K + in methanol-water mixtures and Na + in AN-water mixtures, there was agreement only at lower organic solvent content and the Franks equation predicted higher values for the organic solvent in the primary solvation shell around the cation at higher organic solvent content as compared to experimental results

  14. Isotopic enrichment of 15N by ionic exchange cromatography

    International Nuclear Information System (INIS)

    Trivelin, P.C.O.; Matsui, E.; Salati, E.

    1979-01-01

    The ionic exchange chromatographic method in columns of resin which is employed in the study of isotopic enrichment of 15 N is presented. Determinations are made of the isotopic separation constant for the exchange of isotopes 15 N and 14 N in the equilibrium involving ammonium hidroxide in the solution phase and ions NH 4 + adsorbed in cationic resins: Dowex 50W-X8 and X12, 100-200 mesh. Experiments are also conducted for determination of height of theoretical plates for situations of equilibrium of the NH 4 + band in two systems of resin's columns aimed at estimating the experimental conditions used. The isotopic analyses of nitrogen are carried out by mass spectrometry [pt

  15. Sulfur isotope separation by anion exchange chromatography: 34 S isotope enrichment

    International Nuclear Information System (INIS)

    Bendassolli, Jose Albertino; Trivelin, Paulo Cesar O.; Carneiro Junior, Francisco

    1995-01-01

    The 34 S isotope separation was carried out by isotopic exchange reactions between sulphurous acid in solution and bisulphite anions adsorbed on an ammonium quaternary (Dowex 1 x 8 and Dowex 2 x 8, 100-200 mesh) anion exchange resin packed in columns. Each resin column had 130 cm length and 2.2 cm diameter. The columns were connected in series during displacement of bisulphite bands. For the experiments, a band of bisulphite was fixed to the anion resin, initially in the hydroxyl ion form, and subsequently eluted with 0.2 0.3, 0.4 and 0.6 mol L -1 HCL solution. The hydrochloric acid solution was kept under a nitrogen atmosphere at 245 KPa of pressure, in order to prevent the evolution of gases and also the oxidation of the bisulphite. The experiments showed that the best results were obtained with the elution of bisulphite with 0.2 mol.L -1 HCL, with the Dowex 1 x 8 resin. Enrichments in 34 S of 17.33 atoms% were obtained using Dowex 1 x 8 resin, 0.2 mol.L -1 HCL solution and band displacement of 50 m. Replacing the depleted portion of the band with natural bisulphite, for each 10 m of band displacement, produced 6.79 mmol of sulphurous acid enriched with approximately 17% of 34 S, after 14 m of band dislocation. (author). 7 refs., 1 fig., 2 tabs

  16. Kinetics of destruction of KU-2 x 8 and AV-17 x 8 ion-exchange resins by the joint action of heating and irradiation

    International Nuclear Information System (INIS)

    Tulupov, P.E.; Butenko, T.Yu.

    1982-01-01

    Experimental data indicates a decrease of the exchange capacity of AV-17 x 8 (OH) resin in ion-exchange beds at various temperatures. Losses of exchange of the resin in hydroxyl form after 10,000h of continuous heating at 60, 70, and 80 0 C are 24, 44, and 78% respectively. Partial replacement of the hydroxyl by the salt form is accomplished by appreciable lowering of capacity losses. The trimethlyamine evolved during deamination of AV-17 x 8 anion exchange resin, and only methanol, enters the coolant. Under the influence of ionizing radiation in the active zone the methanol will be converted successively into formaldehyde, formic acid and CO 2 . Thus the maximum temperature of use of the hydroxyl form of te anion-exchange resin AV-17 x 8 (OH) in nuclear power plants can be raised to 70-75 0 C. Brief changes of temperature at 100 0 C do not cause any appreciable losses of exchange capacity either. Physicochemical properties of ion-exchange resins after use in nuclear power plants leads to excessive and unjustified restriction of their service life in the course of a single cycle. Joint action of heating and irradiation on AV-17 anion-exchange resin was studied. It was found that rate constants of the processes of thermal radiation decreases the exchange capacities of the resins in the temperature ranges of interest with relation to nuclear power plants. Calculation of the stability of KU-2 x 8 cation-exchange resin shows that even after a year of use at 100 0 C the loss of its exchange capacity is less than 0.1%. Therefore, under the conditions of use in a nuclear power plant KU-2 x 8 resin can be regarded as absolutely stable. The loss of exchange capacity of AV-17 x 8 resin in C1 form at 100 0 C is of similar magnitude

  17. Isolation of 14C labelled amino acids by biosynthesis in maize plants (Zea mais L.)

    International Nuclear Information System (INIS)

    Carreras, N.; Mazon, M.P.

    1983-01-01

    A method of obtaining 14 C labelled amino acids by biosynthesis in maize plants which had assimilated 14CO 2 , has been assayed. The plants were labelled for 60 minutes with 14 C O2 produced from Ba 14 C O3 (specific activity of 148 KBq/μmol). An extract of the soluble compounds was obtained with 80% ethanol and the amino acids were separated from the rest of the soluble compounds by ion exchange chromatography on column of Dowex 50-X8 resin. Finally, seventeen amino acids were isolated and identified from the purified extract. The acid amino acids were separated in anionic column (Dowex 1-X8) and the neutral and basic amino acids in cationic column (Dowex 50-X4). (Author) 56 refs

  18. Isolation of carbon 14 labelled amino acids by biosynthesis in maize plants (zea mais L.)

    International Nuclear Information System (INIS)

    Carreras, N.; Mazon, M.P.

    1983-01-01

    A method of obtaining 14 C labelled amino acids by biosynthesis in maize plants which had assimilated 14 CO 2 , has been assayed. The plants were labelled for 60 minutes with 14 CO 2 produced from Ba 14 CO 3 (specific activity of 148 KBq/μmol). An extract of the soluble compounds was obtained with 80% ethanol and the amino acids were separated from the rest of the soluble compounds by ion exchange chromatography on column of Dowex 50-X8 resin. Finally, seventeen amino acids were isolated and identified from the purified extract. The acid amino acids were separated in anionic column (Dowex 1-X8) and the neutral and basic amino acids in cationic columns (Dowex 50-X4). (author)

  19. Boron determination in U3O8

    International Nuclear Information System (INIS)

    Ogura, Nadia S.; Sarkis, Jorge E.S.; Rosa, Daniele S.; Ulrich, Joao C.

    2009-01-01

    There exist specifications of the concentration as far the limit of impurities in the used uranium compounds is concerned. Among those impurities the boron element is detached. that in the uranium compounds acts as neutron absorber in nuclear reactions. Therefore, the determination of this element in uranium compounds, it is fundamental for the quality and performance of the nuclear fuels. However, the determination of this element is many times prejudiced by the presence of the uranium. For solving this problem, it is performed a chemical separation of the uranium (matrix) out of the interest. The most used methods to accomplish that separation are the solvent extraction and the ion exchange. In this work, the boron concentration will be done through the ion exchange technique, using polypropylene columns and Dowex AG 50W - X8 100-200 mesh cation resin in chloricide medium 0.25 M. The boron concentration will be determined through high resolution inductive coupling plasma mass spectrometry (HRICP-MS)

  20. Sensitive method for the assay of guanylate cyclase activity

    Energy Technology Data Exchange (ETDEWEB)

    Karczewski, P; Krause, E G [Akademie der Wissenschaften der DDR, Berlin-Buch. Zentralinstitut fuer Herz- und Kreislauf-Regulationsforschung

    1978-07-01

    A method for the assay of guanylate cyclase is described utilizing ..cap alpha..-(/sup 32/P)-GTP as substrate for the enzyme reaction. 100-150 ..mu..g of enzyme protein is incubated in a 15.6 mM Tris-HCl buffer incubation mixture, pH 7.6. The reaction is stopped by the addition of EDTA. The (/sup 32/P)-cyclic GMP formed is separated by a two-step column chromatography on Dowex 50W-X4 ion-exchange resin and neutral alumina. The recovery for cyclic GMP was about 70%. The blank values ranged from 0.001-0.003 % of the added ..cap alpha..-(/sup 32/P)-GTP which had been purified by Dowex 50W-X4 column chromatography. This method was employed for the assay of guanylate cyclase activities in different tissues.

  1. Isolation of 14{sub C} labelled amino acids by biosynthesis in maize plants (Zea mais L.); Obtencin de aminoacidos marcados con 14{sub C} por biosintesis en plantulas de maiz (Zea mais L)

    Energy Technology Data Exchange (ETDEWEB)

    Carreras, N; Mazon, M P

    1983-07-01

    A method of obtaining 14{sub C} labelled amino acids by biosynthesis in maize plants which had assimilated 14CO{sub 2}, has been assayed. The plants were labelled for 60 minutes with 14{sub C}O2 produced from Ba 14{sub C}O3 (specific activity of 148 KBq/{mu}mol). An extract of the soluble compounds was obtained with 80% ethanol and the amino acids were separated from the rest of the soluble compounds by ion exchange chromatography on column of Dowex 50-X8 resin. Finally, seventeen amino acids were isolated and identified from the purified extract. The acid amino acids were separated in anionic column (Dowex 1-X8) and the neutral and basic amino acids in cationic column (Dowex 50-X4). (Author) 56 refs.

  2. Evaluation of {sup 131}I retention in several adsorbers

    Energy Technology Data Exchange (ETDEWEB)

    Catanoso, Marcela F.; Osso Junior, Joao Alberto, E-mail: marcela.forli@gmail.co, E-mail: jaosso@ipen.b [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil). Diretoria de Radiofarmacia

    2011-07-01

    Several iodine radioisotopes are used in nuclear medicine for treatment and diagnostic purposes. The radioisotope {sup 131}I is used both in diagnosis and therapy due to its physical characteristics of decay by {beta}{sup -} and its {gamma}-ray emissions suitable for diagnosis. It is routinely produced at IPEN through the irradiation of TeO{sub 2} targets in the IEA-R1m nuclear reactor. After the irradiation, the {sup 131}I is separated by dry distillation, where the targets are put in an oven, heated at 760 deg C for 2 hours and the {sup 131}I, volatile, is carried by an O{sub 2} gas stream. The aim of this work was to evaluate the retention and elution of {sup 131}I samples produced at IPEN in several adsorbers as part of a project aiming the purification of these radioisotopes, allowing the labeling of biomolecules. Samples of {sup 131}I were used for retention and elution studies with the following adsorbers: commercial cartridges, anionic resin columns and cationic resin column. The results showed that Ag cartridges and anionic resins Dowex 1X8, Dowex 3 and IRA 400 had a great iodine retention but no elution after using specific eluents. The QMA light, acid alumina, neutral alumina and cationic resin Dowex 50WX4 showed high retention and elution and QMA plus and cationic resin Dowex 50WX8 and Dowex 50WX12 had a good retention but lower elution. Regarding to the better retention and elution, Ag cartridges and resins showed a higher percentage of iodine retention but lower elution yield and QMA light, acid and neutral alumina cartridges showed better results. (author)

  3. Evaluation of 131I retention in several adsorbers

    International Nuclear Information System (INIS)

    Catanoso, Marcela F.; Osso Junior, Joao Alberto

    2011-01-01

    Several iodine radioisotopes are used in nuclear medicine for treatment and diagnostic purposes. The radioisotope 131 I is used both in diagnosis and therapy due to its physical characteristics of decay by β - and its γ-ray emissions suitable for diagnosis. It is routinely produced at IPEN through the irradiation of TeO 2 targets in the IEA-R1m nuclear reactor. After the irradiation, the 131 I is separated by dry distillation, where the targets are put in an oven, heated at 760 deg C for 2 hours and the 131 I, volatile, is carried by an O 2 gas stream. The aim of this work was to evaluate the retention and elution of 131 I samples produced at IPEN in several adsorbers as part of a project aiming the purification of these radioisotopes, allowing the labeling of biomolecules. Samples of 131 I were used for retention and elution studies with the following adsorbers: commercial cartridges, anionic resin columns and cationic resin column. The results showed that Ag cartridges and anionic resins Dowex 1X8, Dowex 3 and IRA 400 had a great iodine retention but no elution after using specific eluents. The QMA light, acid alumina, neutral alumina and cationic resin Dowex 50WX4 showed high retention and elution and QMA plus and cationic resin Dowex 50WX8 and Dowex 50WX12 had a good retention but lower elution. Regarding to the better retention and elution, Ag cartridges and resins showed a higher percentage of iodine retention but lower elution yield and QMA light, acid and neutral alumina cartridges showed better results. (author)

  4. Recover of some rare earth elements from leach liquor of the Saghand uranium ore using combined precipitation and cation exchange methods

    International Nuclear Information System (INIS)

    Khanchi, A. R.; Rafati, H.; Rezvaniyanzadeh, M. R.

    2008-01-01

    In this research work, the recovery and separation of La(III), Ce(III), Sm(III), Dy(III) and Nd(III) from Saghand uranium ore have been studied by precipitation and ion-exchange chromatography methods using Dowex 50 W-X 8 cation exchanger. At first, some preliminary and preconcentration experiments such as comminution, sieve analysis, gravity table and electrostatic in preconcentration of lanthanides were performed. Then, acidic digesting and leaching procedure were used. The results of experiments showed that rare earth elements, along with interfering ions such as Al(III), Fe(III), Mg(II) and Mn(II) present in the leach liquor solution. The investigation of separation process by precipitation method revealed that precipitation and then fast separation using centrifugal technique had the best results in the elimination of interference elements. In order to separate the lanthanides and to obtain their elution curves, the chromatographic column containing Dowex 50 W-X 8 resin was employed. For efficient separation of lanthanides from interference elements the hydrochloric acid with concentration of two and six molar was used respectively. Recovery of lanthanides from the leach liquor solution was achieved more than 85%

  5. Ultrafiltration Membrane Fouling and the Effect of Ion Exchange Resins

    KAUST Repository

    Jamaly, Sanaa

    2011-12-01

    Membrane fouling is a challenging process for the ultrafiltration membrane during wastewater treatment. This research paper determines the organic character of foulants of different kinds of wastewater before and after adding some ion exchange resins. Two advanced organic characterization methods are compared in terms of concentration of dissolved organic carbons: The liquid chromatography with organic carbon (LC-OCD) and Shimadzu total organic carbon (TOC). In this study, two secondary wastewater effluents were treated using ultrafiltration membrane. To reduce fouling, pretreatment using some adsorbents were used in the study. Six ion exchange resins out of twenty were chosen to compare the effect of adsorbents on fouling membrane. Based on the percent of dissolved organic carbon’s removal, three adsorbents were determined to be the most efficient (DOWEX Marathon 11 anion exchange resin, DOWEX Optipore SD2 polymeric adsorbent, and DOWEX PSR2 anion exchange), and three other ones were determined to the least efficient (DOWEX Marathon A2 anion exchange resin, DOWEX SAR anion exchange resin, and DOWEX Optipore L493 polymeric adsorbent). Organic characterization for feed, permeate, and backwash samples were tested using LC-OCD and TOC to better understand the characteristics of foulants to prevent ultrafiltration membrane fouling. The results suggested that the polymeric ion exchange resin, DOWEX SD2, reduced fouling potential for both treated wastewaters. All the six ion exchange resins removed more humic fraction than other organic fractions in different percent, so this fraction is not the main for cause for UF membrane fouling. The fouling of colloids was tested before and after adding calcium. There is a severe fouling after adding Ca2+ to effluent colloids.

  6. Studies on {sup 99}Mo-{sup 99m}Tc adsorption and elution behaviors using the inorganic sorbent ceric tungstate and conventional organic resins

    Energy Technology Data Exchange (ETDEWEB)

    El-Sweify, Fatma H.; Fattah, Alaa El-Din A. Abdel; Aly, Shorouk M.; Ghamry, Mohamed A. [Atomic Energy Authority, Cairo (Egypt). Hot Laboratories Center; El-Sheikh, Ragaa [Zagazig Univ. (Egypt). Chemistry Dept.

    2017-09-01

    Adsorption behavior of {sup 99}Mo(VI) and {sup 99m}Tc(VII) was studied on ceric tungstate (CeW) and compared with the adsorption on the conventional cation and anion exchangers Dowex-50X8 and AG-2X8, respectively. The studies were carried out under static and dynamic conditions. The effect of contact time and pH on the adsorption was investigated under static conditions. High K{sub d}-values for sorption of {sup 99}Mo(VI) on (CeW) were obtained over the investigated pH range. {sup 99m}Tc was adsorbed with much lower K{sub d}-values. The K{sub d}-values were pH dependent. K{sub d}-values of {sup 99}Mo-adsorption on AG-2X8 were lower than those on (CeW) and vice versa for {sup 99m}Tc. Ionic species of both elements were not adsorbed on Dowex-50X8, indicating the absence of cationic species and the adsorption of both elements on AG-2X8 and (CeW) as anionic species. The loading and elution behaviors of {sup 99}Mo and {sup 99m}Tc on (CeW) were studied using different eluents. {sup 99}Mo remained strongly adsorbed under all conditions whereas {sup 99m}Tc was easily eluted. Adsorption of some fission products, i.e. {sup 95}Zr(IV) and {sup 95}Nb(V), in addition to {sup 123m}Te(IV) and {sup 75}Se(IV), as representatives of their corresponding fission product isotopes, as well as {sup 181}Hf, as probable radioactive contaminant was also studied. Solutions of the ionic species of those metals were loaded in mixtures together with {sup 99}Mo on (CeW) columns. Strong adsorption of those ionic species and {sup 99}Mo on (CeW) was found whereas {sup 99m}Tc was easily eluted. Different eluents were investigated for eluting {sup 99m}Tc from {sup 99}Mo-adsorbed on (CeW).

  7. Geochemistry of ferromanganese nodule-sediment pairs from central Indian Ocean Basin

    Digital Repository Service at National Institute of Oceanography (India)

    Pattan, J.N.; Parthiban, G.

    analyses and remaining part of the solution was used for rare earth element separation using Dowex AG 50W-X8 (200-400 mesh) ion exchange resin following the procedure of Jarvis and Jarvis (1985). Major, few trace and rare earth elements were analysed... and precision based on duplicate sample analysis were ± 4 %. For total silica measurements, both nodules and sediments were fused with lithium metaborate in a furnace and clear solutions obtained were analysed with ICP-AES. Accuracy was better than ± 4...

  8. Calcium isotope fractionation in ion-exchange chromatography

    International Nuclear Information System (INIS)

    Russell, W.A.; Papanastassiou, D.A.

    1978-01-01

    Significant fractionation of the isotopes of calcium has been observed during elution through short ion-exchange columns packed with Dowex 50W-X8 resin. A double isotopic tracer was used to provide correction for instrumental fractionation effects. The absolute 40 Ca/ 44 Ca ratio is determined by this method to 0.05% and provides a measure of the fractionation of all Ca isotopes. It is found that the lighter isotopes are preferentially retained by the resin, with variations in 40 Ca/ 44 Ca between the first and last fractions of up to 1.1%. An estimate of the separation factor between batch solute and resin gives epsilon = 2.1 x 10 -4 . Details of the chemical or physical mechanisms causing isotope fractionation of Li, Na, Ca, and other elements during ion-exchange chromatography are not yet clear

  9. Raman spectroscopic study of the aging and nitration of actinide processing anion-exchange resins in concentrated nitric acid

    International Nuclear Information System (INIS)

    Buscher, C. T.; Donohoe, R. J.; Mecklenburg, S. L.; Berg, J. M.; Tait, C. D.; Huchton, K. M.; Morris, D. E.

    1999-01-01

    Degradation of two types of anion exchange resins, Dowex 11 and Reillex HPQ, from the action of concentrated nitric acid (4 to 12 M) and radiolysis [from depleted uranium as UO 2 2+ nitrate species and 239 Pu as Pu(IV) nitrate species] was followed as a function of time with Raman vibrational spectroscopy. Elevated temperatures (∼50 degree sign C) were used in the absence of actinide metal loading to simulate longer exposures of the resin to a HNO 3 process stream and waste storage conditions. In the absence of actinide loading, only minor changes in the Dowex resin at acid concentrations ≤10 M were observed, while at 12 M acid concentration, the emergence of a Raman peak at 1345 cm-1 indicates the addition of nitro functional groups to the resin. Similar studies with the Reillex resin show it to be more resistant to nitric acid attack at all acid concentrations. Incorporation of weakly radioactive depleted uranium as the UO 2 2+ nitrate species to the ion-exchange sites of Dowex 11 under differing nitric acid concentrations (6 to 12 M) at room temperature showed no Raman evidence of resin degradation or nitration, even after several hundred days of contact. In contrast, Raman spectra for Dowex 11 in the presence of 239 Pu as Pu(IV) nitrate species reveal numerous changes indicating resin alterations, including a new mode at 1345 cm-1 consistent with a Pu(IV)-nitrate catalyzed addition of nitro groups to the resin backbone. (c) 2000 Society for Applied Spectroscopy

  10. studies on the use of organic and inorganic ion exchangers for separation of indium(III) from cadmium(II) using analytical methods

    International Nuclear Information System (INIS)

    Mohamed, A.A.E.

    2011-01-01

    Organic and inorganic ion exchangers have many applications not only in the industrial, environmental and the nuclear fields but also in the separation of metal ions. This may be returned to its high measured capacity, high selectivity for some metal ions, low solubility, high chemical radiation stability and easy to use.Indium and cadmium are produced from cyclotron target where the solvent extraction represents an ordinary method for separation of indium and cadmium from its target. In the present work, More than chromatographic columns were successfully used for the separation and recovery of indium(III) and cadmium(II) ions from di-component system in aqueous solution using organic and inorganic ion exchangers. The work was carried out in three main parts;1- In the first part, the commercial resin (Dowex50w-x8) was used for the separation of indium from cadmium. The effect of pH, the weight of resin, and equilibrium time on the sorption process of both metal ions were determined. It was found that the adsorption percentage was more than 99% at pH 4 (as optimum pH value) using batch experiment. The results show that indium was first extracted while cadmium is slightly extracted at this pH value. The recovery of indium and cadmium is about 98% using hydrochloric acid as best eluent. The ion exchange/complexing properties of Dowex50w-x8 resin containing various substituted groups towards indium and cadmium cations were investigated.2- In the second part, Zn(II)polymethacrylates, and poly (acrylamide-acrylic acid), as synthetic organic ion exchangers were prepared by gamma irradiation polymerization technique of the corresponding monomer at 30 kGy. The obtained organic resins were mixed with indium ions to determine its capacity in aqueous solutions using batch experiment.

  11. Bisulphite complexation in the resin catalysed epimerisation of D-fructose-radiotracer investigations [Paper No. AR-27

    International Nuclear Information System (INIS)

    Murlidharan, B.; Mallika, S.; Viswanathan, K.V.

    1982-01-01

    Tracer methods were used to study the conversion of D-Fructose- 16 C to its aldose epimers. D-Fructose- 14 C sorbed on Dowex-1-X8(OH - form) columns on elution with dilute sulphurous acid (>0.1M) was converted mainly to D-Glucose- 14 C accompanied by excessive degradation. Treatment of D-Fructose- 14 C with Dowex-1-X4 in carbonate and bisulphite forms at 50degC in 50 per cent ethanol gave an epimeric mixture containing more than 25 per cent of D-Mannose- 14 C. (author)

  12. Preparation of curium-americium oxide microspheres by resin-bead loading

    International Nuclear Information System (INIS)

    Chattin, F.R.; Benker, D.E.; Lloyd, M.H.; Orr, P.B.; Ross, R.G.; Wiggins, J.T.

    1980-01-01

    Resin-bead loading and calcination techniques have been used to produce all curium and americium oxide feed material (about 2.2 kg) for HFIR targets since 1971. The process based on Dowex 50W resin has progressed from a series of test runs, through special production runs, into routine production in permanent equipment beginning in 1975. Key attributes of this process are its reliability, high yields, and ease of operation. The process is suited for remote operation in hot cells. Yields approaching 95% are routinely obtained and only one unacceptable product has been generated during routine production operations. There have been no problems in fabricating targets from this oxide or in the subsequent irradiation of these targets. The present scale of production of 150 to 250 g/y supplies the present need and is comparable with the level of other chemical process operations at TRU. Since the annual production is accomplished in two 8 to 12 day periods, there has been no reason to consider further scale-up. However, the rate of production could easily be doubled by simply adding a second set of calcination equipment

  13. Enhancement of uranium loading on ion exchange resin from carbonate leachate by lowering pH from 8 to 6.5

    International Nuclear Information System (INIS)

    Otto, J.B.

    1984-01-01

    This paper discusses a laboratory study that shows the saturation ion-exchange loading of uranium from carbonate leachate can be doubled by lowering the pH of the leachate from 8 to 6.5. Small column and batch resin loading tests using Dowex 21K ion-exchange resin are described. The leachate contained 3,300 ppm chloride, 2,400 ppm carbonate, and 220 ppm U 3 O 8 , and had a pH of 8. Even at this rather mild salinity the saturation ion-exchange loading was found to be only about 3 to 4 lbm U 3 O 8 /cu ft resin (48 to 64 g/dm 3 ) because of competition with the chloride ion for exchange sites on the anionic resin. Lowering the pH of the leachate to 6.5 by CO 2 gas addition, however, increased loading to about 8 lbm U 3 O 8 /cu ft resin (128 g/dm 3 ). The pH-lowering effect worked especially well at relatively high salt concentration. The same leachate, with its chloride content increased to 12,000 ppm, loaded only 0.5 lbm U 3 O 8 /cu ft resin (8 g/dm 3 ) at pH 8 but loaded 5.5 lbm U 3 O 8 /cu ft resin (88 g/dm 3 ) at pH 6.5

  14. Complex ion kinetics. Reaction rates on ion-exchange resins compared to those in water

    International Nuclear Information System (INIS)

    Liss, I.B.; Murmann, R.K.

    1975-01-01

    A comparison has been made between the rates in water and on an ion-exchange resin for the aquation of [(NH 3 ) 5 CoOReO 3 ] 2+ and [(H 2 O) 5 CrCl] 2+ and for the 18 O isotopic exchange of water with [(NH 3 ) 5 Co(OH 2 )] 3+ and ReO 4 - . The rate of water exchange on [(NH 3 ) 5 Co(OH 2 )] 3+ was not changed by association with Dowex 50W resins. Aquation of [(NH 3 ) 5 CoOReO 3 ] 2+ and water exchange on ReO 4 - had modified pH dependencies when associated with a resin. With the cobalt complex the rates were faster on the resin in the acidic region and slower on the resin in the basic region. A new term in the rate equation was observed when ReO 4 - was on the resin, first order in H + , while the other terms appear to be unchanged. Aquation of [(H 2 O) 5 CrCl] 2+ was much slower when it was absorbed on the resin. This was related to the known ionic strength effect of the reaction. (auth)

  15. Boron removal from aqueous solutions by ion-exchange resin: Column sorption-elution studies

    International Nuclear Information System (INIS)

    Koese, T. Ennil; Oztuerk, Nese

    2008-01-01

    A column sorption-elution study was carried out by using a strong base anion-exchange resin (Dowex 2 x 8) for the removal of boron from aqueous solutions. The breakthrough curve was obtained as a function of feed flow rate and the total and breakthrough capacity values of the resin were calculated. The boron on the resin was quantitatively eluted with 0.5 M HCl solution at different flow rates. Three consecutive sorption-elution-washing-regeneration-washing cycles were applied to the resin in order to investigate the reusability of the ion-exchange resin. Total capacity values remained almost the same after three sorption-elution-regeneration cycles. The Thomas and the Yoon-Nelson models were applied to experimental data to predict the breakthrough curves and to determine the characteristic column parameters required for process design. The results proved that the models would describe the breakthrough curves well

  16. Exchange of Th, U and Pu on macroporous ion exchange resins

    International Nuclear Information System (INIS)

    Nadkarni, M.N.; Mayankutty, P.C.; Pillai, N.S.; Shinde, S.S.

    1977-01-01

    Absorption of Th, U and Pu on macroporous ion exchangers, Amberlyst 15 (cationic) and Amberlyst A-26 (anionic) were studied in nitric acid solutions and the results were found comparable with those on their microreticular counter parts, Dowex 50x8 and Dowex IX4. With a view to evalute the efficiency of Amberlyst A-26 for the final purification of plutonium from the purex process stream, detailed studies conducted to determine the breakthrough capacity of Pu(IV) from 7.2 M nitric acid, elution by 0.5 M nitric acid and the decontamination factors for uranium and zirconium-95. Because of its faster kinetics, Amberlyst A-26 exhibited a much more efficient elution of Pu(IV) by 0.5 M nitric acid than Dowex IX4. (author)

  17. Preparation of microcuries of 234-thorium

    International Nuclear Information System (INIS)

    Suner, A.; La Gamma de Batistoni, A.M.; Botbol, J.

    1974-11-01

    A procedure for the preparation of microcuries of 234 Th from hydrochloric acid solutions of uranium (VI) is described. A solution of uranyl chloride in radioactive equilibrium with 234 Th (older than 6 months) and having 232 Th as carrier, is percoled through a Dowex 50 Wx8 (H + ) resin bed, wherein is absorbed 85% of Th and some uranium, which is then desorbed with 10 N HCl. The thorium remains in the column and is extracted later with a 0,025 M SO 4 H 2 plus 1 M SO 4 (NH 4 ) 2 solution. The thorium solution is freed from sulfate by precipitation with ammonia, dissolving the precipitate with 10 N HCl, whose solution is treated with Dowex 2x8 resin. The ion exchanger absorbs the anionic impurities and the thorium obtained is of high chemical and radiochemical purity. (author)

  18. Novel solid phase extraction procedure for gold(III) on Dowex M 4195 prior to its flame atomic absorption spectrometric determination

    Energy Technology Data Exchange (ETDEWEB)

    Tuzen, Mustafa [Gaziosmanpasa University, Faculty of Science and Arts, Chemistry Department, 60250 Tokat (Turkey)], E-mail: mtuzen@gop.edu.tr; Saygi, Kadriye O. [Gaziosmanpasa University, Faculty of Science and Arts, Chemistry Department, 60250 Tokat (Turkey); Soylak, Mustafa [Erciyes University, Faculty of Science and Arts, Chemistry Department, 38039 Kayseri (Turkey)

    2008-08-15

    A method for solid phase extraction (SPE) of gold(III) using Dowex M 4195 chelating resin has been developed. The optimum experimental conditions for the quantitative sorption of gold(III), pH, effect of flow rates, eluent types, sorption capacity and the effect of diverse ions on the sorption of gold(III) have been investigated. The chelating resin can be reused for more than 100 cycles of sorption-desorption without any significant change in sorption of gold(III) ions. The recovery values for gold(III) and detection limit (LOD) of gold were greater than 95% and 1.61 {mu}g L{sup -1}, respectively. The preconcentration factor was 31. The relative standard deviation of the method was <5%. The adsorption capacity of the resin was 8.1 mg g{sup -1}. The proposed method has been applied for the determination of gold(III) in some real samples including water, soil and sediment samples.

  19. Batch and column adsorption behaviors of Se(IV) and Te(IV) on organic and inorganic ion exchangers from HCl solutions

    Energy Technology Data Exchange (ETDEWEB)

    El-Sweify, Fatma H.; Abdel-Fattah, Alaa El-Din A.; Aly, Shorouk M.; Ghamry, Mohamed A. [Atomic Energy Authority, Cairo (Egypt). Hot Laboratories Center; El-Sheikh, Ragaa [Zagazig Univ. (Egypt). Chemistry Dept.

    2017-07-01

    Adsorption behaviors of Se(IV) and Te(IV) on the inorganic ion exchanger ceric tungstate (CeW) was studied under static and dynamic conditions and compared with the adsorption on the organic cation and anion exchangers Dowex-50X8 and AG-2X8, respectively. The radioactive isotopes {sup 75}Se and {sup 123m}Te were used to trace the respective elements. Some parameters affecting the adsorption were investigated under static conditions. In the case of batch technique the adsorption was studied from slightly acidic HCl as well as slightly alkaline media, i.e. at two pH-ranges. Se(IV) and Te(IV) were adsorbed on both the inorganic ion exchanger (CeW) and on AG-2X8, from slightly alkaline solutions. From the similarity of adsorption on both ion exchangers it was clear that (CeW) acts as an anion exchanger. Moreover, the obtained K{sub d}-values for the adsorption on (CeW) were much higher than those for the adsorption on the organic anion exchanger AG-2X8. Se(IV) was not adsorbed on Dowex-50X8 all over the studied pH-range whereas Te(IV) was slightly adsorbed. Loading and elution behaviors of Se(IV) and Te(IV) on columns of AG-2X8 and (CeW) were studied using solutions of HCl of different concentrations. Some good separation alternatives of Se(IV) and Te(IV) under certain conditions were achieved.

  20. Sorption behaviour of W, Hf, Lu, U, and Th on ion exchangers from HCl/H2O2 solutions. Model experiments for chemical studies of seaborgium (Sg)

    International Nuclear Information System (INIS)

    Schumann, D.; Andrassy, M.; Nitsche, H.; Misiak, R.; Schaedel, M.; Bruechle, W.; Schausten, B.; Kratz, J.V.

    1997-08-01

    In model experiments with W, Hf, Th, and U radionuclides, a chemical system was developed for the separation of seaborgium from element 104 and heavy actinides, i.e., cation exchange on DOWEX 50 x 8 from solutions containing 0.1-1.0 M HCl and 0.5-2.0 vol.% H 2 O 2 . The system should be suitable for fast on-line experiments if seaborgium exibits a non-uranium-like behaviour. Adding hydrogen peroxide to mixed HCl/HF solutions suppresses the partial sorption of W and, presumably seaborgium, on the cation exchanger. This way, the elution volume can be minimized. Prospects for anion exchange separations of group 6 from 4 elements are also briefly discussed. (orig.)

  1. Thermal cycling effects on adhesion of resin-bovine enamel junction among different composite resins.

    Science.gov (United States)

    Chen, Wen-Cheng; Ko, Chia-Ling; Wu, Hui-Yu; Lai, Pei-Ling; Shih, Chi-Jen

    2014-10-01

    Thermal cycling is used to mimic the changes in oral cavity temperature experienced by composite resins when used clinically. The purpose of this study is to assess the thermal cycling effects of in-house produced composite resin on bonding strength. The dicalcium phosphate anhydrous filler surfaces are modified using nanocrystals and silanization (w/NP/Si). The resin is compared with commercially available composite resins Filtek Z250, Z350, and glass ionomer restorative material GIC Fuji-II LC (control). Different composite resins were filled into the dental enamel of bovine teeth. The bond force and resin-enamel junction graphical structures of the samples were determined after thermal cycling between 5 and 55°C in deionized water for 600 cycles. After thermal cycling, the w/NP/Si 30wt%, 50wt% and Filtek Z250, Z350 groups showed higher shear forces than glass ionomer GIC, and w/NP/Si 50wt% had the highest shear force. Through SEM observations, more of the fillings with w/NP/Si 30wt% and w/NP/Si 50wt% groups flowed into the enamel tubule, forming closed tubules with the composite resins. The push-out force is proportional to the resin flow depth and uniformity. The push-out tubule pore and resin shear pattern is the most uniform and consistent in the w/NP/Si 50wt% group. Accordingly, this developed composite resin maintains great mechanical properties after thermal cycling. Thus, it has the potential to be used in a clinical setting when restoring non-carious cervical lesions. Copyright © 2014 Elsevier Ltd. All rights reserved.

  2. Diclofenac removal in urine using strong-base anion exchange polymer resins.

    Science.gov (United States)

    Landry, Kelly A; Boyer, Treavor H

    2013-11-01

    One of the major sources of pharmaceuticals in the environment is wastewater effluent of which human urine contributes the majority of pharmaceuticals. Urine source separation has the potential to isolate pharmaceuticals at a higher concentration for efficient removal as well as produce a nutrient byproduct. This research investigated the efficacy of using strong-base anion exchange polymer resins to remove the widely detected and abundant pharmaceutical, diclofenac, from synthetic human urine under fresh and ureolyzed conditions. The majority of experiments were conducted using a strong-base, macroporous, polystyrene resin (Purolite A520E). Ion-exchange followed a two-step removal rate with rapid removal in 1 h and equilibrium removal in 24 h. Diclofenac removal was >90% at a resin dose of 8 mL/L in both fresh and ureolyzed urine. Sorption of diclofenac onto A520E resin was concurrent with desorption of an equivalent amount of chloride, which indicates the ion-exchange mechanism is occurring. The presence of competing ions such as phosphate and citrate did not significantly impact diclofenac removal. Comparisons of three polystyrene resins (A520E, Dowex 22, Dowex Marathon 11) as well as one polyacrylic resin (IRA958) were conducted to determine the major interactions between anion exchange resin and diclofenac. The results showed that polystyrene resins provide the highest level of diclofenac removal due to electrostatic interactions between quaternary ammonium functional groups of resin and carboxylic acid of diclofenac and non-electrostatic interactions between resin matrix and benzene rings of diclofenac. Diclofenac was effectively desorbed from A520E resin using a regeneration solution that contained 4.5% (m/m) NaCl in an equal-volume mixture of methanol and water. The greater regeneration efficiency of the NaCl/methanol-water mixture over the aqueous NaCl solution supports the importance of non-electrostatic interactions between resin matrix and benzene rings

  3. 40 CFR 414.50 - Applicability; description of the thermosetting resins subcategory.

    Science.gov (United States)

    2010-07-01

    ... thermosetting resins subcategory. 414.50 Section 414.50 Protection of Environment ENVIRONMENTAL PROTECTION... Thermosetting Resins § 414.50 Applicability; description of the thermosetting resins subcategory. The provisions... the products classified under SIC 28214 thermosetting resins including those resins and resin groups...

  4. Adsorption behavior of 99Mo using AG1-X8 anionic resin

    International Nuclear Information System (INIS)

    Santos, Jacinete L. dos; Yamaura, Mitiko; Damasceno, Marcos O.; Forbicini, Christina A.L.G.O.

    2013-01-01

    The significant growth in demand of 99 Mo in developed and developing countries, like Brazil, requires large production capacity and availability of this radioisotope. With the global crisis on its supply to Brazil rethought the need to become independent in their production and the solution was to start the Brazilian Multipurpose Reactor (RMB) project, which aims to meet the national demand of 99 Mo for the medical field. This work aims to study the 99 Mo adsorption in AG1-X8 strong anion resin, which is one of the intermediate steps of separation and purification, retaining it in the form of molybdate ions. In process evaluated the resin properties with respect to pH and concentration of 99 Mo in the solution. The adsorbed amount of 99 Mo was determined indirectly by the amount in the supernatant after adsorption and the data fitted to the Langmuir and Freundlich isotherms. Among the models, the Langmuir showed a closer relationship with the experimentally obtained data. This suggests the occurrence of monolayer adsorption and heterogeneous conditions at the surface, where both phenomena can coexist in the experimental conditions tested. (author)

  5. Separation of metal ions by anion exchange in mixtures of hydrochloric acid and hydrofluoric acid

    International Nuclear Information System (INIS)

    Faris, J.P.

    1978-12-01

    Distribution coefficients were determined for the adsorption of more than 40 elements on anion-exchange resins from mixtures of HCl (0.1 to 12M) and HF (0.1-8M). Two resins, Dowex 1 x 10, 200 to 400 mesh and Dowex 1 x 4, 100 to 200 mesh, were used. Distribution coefficients were also determined for the adsorption of many elements on both resins from 0.1 to 12M HCl and 0.1 to 12M HF. Anion exchange in the presence of HF was found useful for separating impurities from various materials for their subsequent determination, and specific procedures used in our spectrochemical laboratory for this purpose are outlined. The results of a literature search on the use of anion exchange in hydrofluoric acid and fluoride-containing media are presented in an extensive bibliography. 404 references, 9 tables

  6. Separation and purification of Molybdenum-99 using the AG1x8 and Chelex-100 resins

    International Nuclear Information System (INIS)

    Sanchez M, V.; Lopez C, R.; Millan S, S.; Fucugauchi, L.A.

    1991-05-01

    In the separation of the fission products of the molybdenum-99 soluble in watery solution of sodium hydroxide its have been used advantageously ion exchange processes with resins, which present a great stability toward the oxidizers and reducers agents as well as toward the ionizing radiation. The main stages of the recovery process of Mo-99 starting from the fission products of U-235 enriched. The first step of the purification is the elimination of the alumina taken place in the alkaline breakup of the badges of alloy uranium-aluminum. For it is used it a resin of anion exchange denominated AG1X8. The second stage of the consistent process in the elimination of the remaining fission products that accompany the one Mo-99, by means of the use of the exchange resin Chelex-100. Lastly is carried out the a sublimation process to obtain the pure Mo-99. (Author)

  7. Determination of Hf, Sc and Y in geological samples together with the rare-earth elements

    International Nuclear Information System (INIS)

    Lihareva, N.; Delaloye, M.

    1997-01-01

    A method is described for the determination of Hf, Sc and Y simultaneously with the REE in geological materials. An earlier method for REE separation from major elements was studied with the aim to apply it also to the determination of Hf, Sc and Y. Sample decomposition was carried out by melting with LiBO 2 . The method involves separation and concentration stages, using the cation-exchange resin DOWEX AG 50W-X8. Matrix elements were eluted with 2 mol/l HCl, whereas 6 mol/l HNO 3 with oxalic acid and 8 mol/l HNO 3 were used to elute the elements to be determined. Some of the matrix elements could not be completely removed. This effect as well as the recovery rates of the determined elements were investigated. The measurements were performed by ICP-AES. Spectral interferences were also tested. (orig.). With 1 tab

  8. Synthesis of DL-adrenaline (methyl C{sup 14}) (1961); Synthese de la DL-adrenaline (methyle {sup 14}C) (1961)

    Energy Technology Data Exchange (ETDEWEB)

    Pichat, L; Audinot, M [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1961-07-01

    The sodium derivative of 5-3-4 dibenzyl oxyphenyl 2-oxazolidinone reacted with methyl iodide {sup 14}C, in stoichiometric quantity, gives rise to the corresponding N-methyl {sup 14}C derivative. The oxazolidinone ring is opened by concentrated hydrochloric acid and the benzyl groups removed by catalytic hydrogenolysis. Adrenaline methyl {sup 14}C is then purified on Dowex 50 X-12 exchange resin. Overall-yield is 45 per cent based upon methyl iodide {sup 14}C. (author) [French] Le derive sode de la (dibenzyloxy-3-4-phenyl)-5 oxazolidinone-2 traite par l'iodure de methyle {sup 14}C, en proportion stoechiometrique, fournit le derive N-methyle {sup 14}C correspondant. Apres ouverture du cycle oxazolidinone par HCL concentre et debenzylation par hydrogenation catalytique, on purifie l'adrenaline (methyle {sup 14}C) par chromatographie sur resine echangeuse Dowex 50 X-12. Le rendement est de 45 pour cent par rapport a l'iodure de methyle {sup 14}C. (auteurs)

  9. Synthesis of DL-adrenaline (methyl C{sup 14}) (1961); Synthese de la DL-adrenaline (methyle {sup 14}C) (1961)

    Energy Technology Data Exchange (ETDEWEB)

    Pichat, L.; Audinot, M. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1961-07-01

    The sodium derivative of 5-3-4 dibenzyl oxyphenyl 2-oxazolidinone reacted with methyl iodide {sup 14}C, in stoichiometric quantity, gives rise to the corresponding N-methyl {sup 14}C derivative. The oxazolidinone ring is opened by concentrated hydrochloric acid and the benzyl groups removed by catalytic hydrogenolysis. Adrenaline methyl {sup 14}C is then purified on Dowex 50 X-12 exchange resin. Overall-yield is 45 per cent based upon methyl iodide {sup 14}C. (author) [French] Le derive sode de la (dibenzyloxy-3-4-phenyl)-5 oxazolidinone-2 traite par l'iodure de methyle {sup 14}C, en proportion stoechiometrique, fournit le derive N-methyle {sup 14}C correspondant. Apres ouverture du cycle oxazolidinone par HCL concentre et debenzylation par hydrogenation catalytique, on purifie l'adrenaline (methyle {sup 14}C) par chromatographie sur resine echangeuse Dowex 50 X-12. Le rendement est de 45 pour cent par rapport a l'iodure de methyle {sup 14}C. (auteurs)

  10. 78 FR 63570 - Proposed Collection; Comment Request for Forms W-8BEN, W-8BEN-E, W-8ECI, W-8EXP, and W-8IMY

    Science.gov (United States)

    2013-10-24

    ... W-8BEN, W-8BEN-E, W-8ECI, W-8EXP, and W-8IMY AGENCY: Internal Revenue Service (IRS), Treasury..., the IRS is soliciting comments concerning Form W-8BEN, Certificate of Foreign Status of Beneficial Owner for United States Tax Withholding, Form W-8BEN-E, Certificate of Status of Beneficial Owner for...

  11. Kinetic investigation of the immobilization of chromotropic acid derivatives onto anion exchange resin

    Directory of Open Access Journals (Sweden)

    Savić Jasmina

    2007-01-01

    Full Text Available The adsorption kinetics of pyrazol- (РАСА and imidazol-azo-chromo-tropic acid (IACA onto Dowex 1-X8 resin, as a function of the dye concentration and temperature were investigated at pH 4.5. The pseudo-first- and second-order kinetic models and intraparticle diffusion model were used to describe the obtained kinetic data. The adsorption rate constants were found to be in the order of magnitude 10-2 min-1 for all of the used kinetics models. The adsorption capacity increases with increasing initial dye concentration. The study of adsorption kinetics at different temperatures (in the range from 5 to 25 °C reveals an increase in the rate of adsorption and adsorption capacity with increasing temperature. The activation energy (in the case of РАСА 16.6 kJ/mol, and for IACA 11.3 kJ/mol was determined using the Arrhenius dependence. Electrostatic interactions between the dye and resin beads were shown to be the adsorption mechanism.

  12. Separation of lithium isotopes on ion exchangers; Separation des isotopes du lithium sur echangeurs d'ions

    Energy Technology Data Exchange (ETDEWEB)

    Menes, F; Saito, E; Roth, E [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1958-07-01

    A survey of the literature shows that little information has been published on the separation of lithium isotopes with ion exchange resins. We have undertaken a series of elutions using the ion-exchange resins 'Dowex 50 x 12' and IRC 50, and various eluting solutions. Formulae derived from the treatment of Mayer and Tompkins permit the calculation of the separation factor per theoretical plate. For the solutions tried out in our experiments the separation factors lie in the interval 1.001 to 1.002. These values are quite low in comparison to the factor 1.022 found by Taylor and Urey for ion exchange with zeolites. (author) [French] Nous avons trouve relativement peu de donnees dans la litterature scientifique sur la separation des isotopes de lithium par les resines echangeuses d'ions. Nous avons effectue un certain nombre d'essais sur Dowex 50 X 12 et IRC 50 utilisant divers eluants. Des formules derivees de celles de Mayer et Tompkins permettent le calcul du coefficient de separation par plateau theorique. Pour les eluants etudies, ces facteurs de separation se trouvent entre 1,001 et 1,002. Ces valeurs sont faibles en comparaison du facteur 1,022 trouve par Taylor et Urey pour les zeolithes. (auteur)

  13. Removal method of fluorescent dyes as pretreatment for measurement of major ion concentrations and hydrogen and oxygen isotopic ratios

    International Nuclear Information System (INIS)

    Nakata, Kotaro; Hasegawa, Takuma; Kashiwaya, Koki; Kodama, Hiroki; Miyajima, Tohru

    2011-01-01

    The major ion concentration and isotope ratio of hydrogen and oxygen can provide important information for migration of groundwater. Sometimes, quantitative estimation of these chemical and isotopic characteristics of solution is necessary for groundwater containing fluorescent dyes, which are used in drilling borehole and tracer experiments. However, sometimes correct estimation is disturbed by dyes and they become a cause of troubles for measurement equipments. Thus development of method to remove dyes is required so that the characteristics of groundwater can be estimated without the negative effect of dyes on measurement or equipments. In this study, removal of four representative dyes (Uranin, Eosin, Naphthalenesulfonic acid sodium(NAP) and Amino G acid potassium salt (AG)) was investigated. Uranin and Eosin were found to be removed by non-ionic synthetic resin: HP2MG. 99.99% of the dyes were removed from initial solutions containing dyes with 10 mg/L after contact with resin, while the contact had little effect on ion concentrations and oxygen and hydrogen isotope ratios. Thus the chemical and isotopic characteristics of groundwater samples containing Uranin and Eosin can be obtained by using the HP2MG resin. On the other hand, the NAP and AG were found to be difficult to remove by the HP2MG resin but they were able to be removed by anion exchange resin (Dowex 1x8). Though contact of solution with Dowex 1x8 did not affect cation concentrations and hydrogen and oxygen isotope ratios, anion concentrations were changed by the contact. Therefore the Dowex 1x8 is only applicable to estimation of the cation concentrations and isotope ratio of hydrogen and oxygen. When both anion and cation concentrations from the samples were necessary, Uranin or Eosin were recommended as a tracer in drilling or tracer experiments. (author)

  14. Design principles for handmade electrical insulation of superconducting joints in W7-X

    Energy Technology Data Exchange (ETDEWEB)

    Rummel, K., E-mail: kerstin.rummel@ipp.mpg.de [Max Planck Institute for Plasma Physics, EURATOM Association, Wendelsteinstr. 1, 17491 Greifswald (Germany); John, A. [Max Planck Institute for Plasma Physics, EURATOM Association, Wendelsteinstr. 1, 17491 Greifswald (Germany); Sulek, Z. [Henryk Niewodniczanski Institute of Nuclear Physics, Polish Academy of Sciences, Krakow, Radzikowskiego 152 (Poland)

    2013-10-15

    Highlights: ► In W-7X there are several types of handmade electrical insulation. ► In general insulation based on impregnated glass tapes and special G10 pieces. ► A proper overlapping of glass tapes turned out to be mandatory. ► Detailed qualification and training helps to minimize the failure rate. ► Visual inspection and Paschen tests after every insulation steps are important. -- Abstract: The superconducting magnet system of the Wendelstein 7-X (W7-X) experiment consists of 50 non-planar and 20 planar coils, 121 bus bars and 14 current leads. The connection between bus bars, coils and current leads will be provided by 198 joints. The joints have to be insulated manually during the assembly of the machine in constraint positions and a tight environment. In general the insulation is based on glass tapes impregnated with epoxy resin and special G10 insulating pieces embedded in the glass tape insulation. In critical areas Kapton{sup ®}-foils are embedded in the insulation. All types of insulation were qualified at mock-ups in a 1:1 model of the expected environment in W7-X. The qualification programme comprises thermal cycling between room temperature and 77 K and high voltage tests under air, under vacuum and under reduced pressure (Paschen test). The paper describes the main principles used for different types of handmade Paschen-tight insulations in W7-X and the visual and electrical tests during and after assembly.

  15. Adsorption behavior of {sup 99}Mo using AG1-X8 anionic resin

    Energy Technology Data Exchange (ETDEWEB)

    Santos, Jacinete L. dos; Yamaura, Mitiko; Damasceno, Marcos O.; Forbicini, Christina A.L.G.O., E-mail: jlsantos@ipen.br, E-mail: myamaura@ipen.br, E-mail: marcos956@bol.com.br, E-mail: cforbici@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2013-07-01

    The significant growth in demand of {sup 99}Mo in developed and developing countries, like Brazil, requires large production capacity and availability of this radioisotope. With the global crisis on its supply to Brazil rethought the need to become independent in their production and the solution was to start the Brazilian Multipurpose Reactor (RMB) project, which aims to meet the national demand of {sup 99}Mo for the medical field. This work aims to study the {sup 99}Mo adsorption in AG1-X8 strong anion resin, which is one of the intermediate steps of separation and purification, retaining it in the form of molybdate ions. In process evaluated the resin properties with respect to pH and concentration of {sup 99}Mo in the solution. The adsorbed amount of {sup 99}Mo was determined indirectly by the amount in the supernatant after adsorption and the data fitted to the Langmuir and Freundlich isotherms. Among the models, the Langmuir showed a closer relationship with the experimentally obtained data. This suggests the occurrence of monolayer adsorption and heterogeneous conditions at the surface, where both phenomena can coexist in the experimental conditions tested. (author)

  16. Comparative study using different resins to determine thorium isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Rosa, Mychelle M.L.; Silva, Paulo S.C.; Maihara, Vera A., E-mail: my_linhares@yahoo.com.br, E-mail: pscsilva@ipen.br, E-mail: vmaihara@ipen.br [Instituto de Pesquisas Energéticas e Nucleares (IPEN/CNEN-SP), São Paulo, SP (Brazil); Taddei, Maria Helena T., E-mail: mhtaddei@cnen.gov.br [Comissão Nacional de Energia Nuclear (LAPOC/CNEN), Poços de Caldas, MG (Brazil). Laboratório de Pocos de Caldas; Cheberle, Luan T.V., E-mail: luancheberle@gmail.com [Ambientis Radioproteção, Barueri, SP (Brazil)

    2017-07-01

    Thorium is a naturally occurring radioactive element that is widely distributed in the crust of the Earth. This element is very common in mineral formations in regions with high levels of natural radioactivity, therefore, its determination in environmental samples is important. Thorium isotopes ({sup 228}Th, {sup 230}Th, and {sup 232}Th) were determined in a reference material, the IAEA Soil 327 sample, to validate the two methods employed using different resins. The initial preparation with acid dissolution is the same to both, in the first is used anion exchange resin (DOWEX 1 x 2) and electrodeposition in silver planchets. And in the second method is used a specific chromatographic resin (TEVA) and cerium fluoride microprecipitation. At the end both analysis are quantified by alpha spectrometry. The two methods the results obtained were satisfactory for the reference material used, with relative error of less than 4% for {sup 228}Th, {sup 230}Th, and {sup 232}Th. The main differences found between them were spectrums resolutions, time and cost of analysis. (author)

  17. 75 FR 38179 - Proposed Collection; Comment Request for Forms W-8BEN, W-8ECI, W-8EXP, and W-8IMY

    Science.gov (United States)

    2010-07-01

    ... W-8BEN, W-8ECI, W- 8EXP, and W-8IMY AGENCY: Internal Revenue Service (IRS), Treasury. ACTION: Notice... soliciting comments concerning Form W-8BEN, Certificate of Foreign Status of Beneficial Owner for United States Tax Withholding, Form W-8ECI, Certificate of Foreign Person's Claim for Exemption From Withholding...

  18. Determination of kinetic parameters of heterogeneous isotopic exchange reaction

    International Nuclear Information System (INIS)

    Huang, Ting-Chia; Tsai, Fuan-Nan

    1977-01-01

    A mathematical model has been proposed for a heterogeneous isotopic exchange reaction which involves film diffusion, surface chemical reaction and intraparticle diffusion. The exchange equation to predict the exchange fraction as a function of time for the spherical particles immersed in a solution of finite volume has been derived. The relations between the exchange fraction and dimensionless time are plotted with xi(=ak sub(f)/KD sub(e)), xi 1 (=K 1 a 2 /D sub(e)) and final fractional uptake as parameters. From the values of the kinetic parameters xi and xi 1 , the relative importance of each limiting step is discussed. Experimental results of the isotopic exchange reaction of calcium ion in both system CaCO 3 (s)/Ca 2+ (aq) and system calcium type resin Dowex 50W-X8/Ca 2+ (aq) are coincident with the theoretical equation proposed in this study. (auth.)

  19. Evaluation of the polymerization shrinkage of experimental flowable composite resins through optical coherence tomography

    Science.gov (United States)

    Carneiro, Vanda S. M.; Mota, Cláudia C. B. O.; Souza, Alex F.; Cajazeira, Marlus R. R.; Gerbi, Marleny E. M. M.; Gomes, Anderson S. L.

    2018-02-01

    This study evaluated the polymerization shrinkage of two experimental flowable composite resins (CR) with different proportions of Urethane dimethacrylate (UDMA)/triethylene glycol dimethacrylate (TEGDMA) monomers in the organic matrix (50:50 and 60:40, respectively). A commercially available flowable CR, Tetric N-Flow (Ivoclair Vivadent, Liechtenstein, Germany), was employed as the control group. The resins were inserted in a cylindrical teflon mold (7 mm diameter, 0.6 mm height) and scanned with OCT before photoactivation, immediately after and 15 minutes after light-curing (Radii-Cal, SDI, Australia, 1,200 mW/cm2 ) exposure. A Callisto SD-OCT system (Thorlabs Inc, USA), operating at 930 nm central wavelength was employed for imaging acquisition. Cross-sectional OCT images were captured with 8 mm transverse scanning (2000x512 matrix), and processed by the ImageJ software, for comparison between the scanning times and between groups. Pearson correlation showed significant shrinkage for all groups in each time analyzed. Kruskal-Wallis test showed greater polymerization shrinkage for the 50:50 UDMA/TEGDMA group (p=0.001), followed by the control group (p=0.018). TEGDMA concentration was proportionally related to the polymerization shrinkage of the flowable composite resins.

  20. Novel solid phase extraction procedure for gold(III) on Dowex M 4195 prior to its flame atomic absorption spectrometric determination

    International Nuclear Information System (INIS)

    Tuzen, Mustafa; Saygi, Kadriye O.; Soylak, Mustafa

    2008-01-01

    A method for solid phase extraction (SPE) of gold(III) using Dowex M 4195 chelating resin has been developed. The optimum experimental conditions for the quantitative sorption of gold(III), pH, effect of flow rates, eluent types, sorption capacity and the effect of diverse ions on the sorption of gold(III) have been investigated. The chelating resin can be reused for more than 100 cycles of sorption-desorption without any significant change in sorption of gold(III) ions. The recovery values for gold(III) and detection limit (LOD) of gold were greater than 95% and 1.61 μg L -1 , respectively. The preconcentration factor was 31. The relative standard deviation of the method was -1 . The proposed method has been applied for the determination of gold(III) in some real samples including water, soil and sediment samples

  1. Photoluminescence of trivalent rare earths in perovskite stacking polytypes Ba/sub 2/Lasub(2-x)REsub(x)/sup 3 +/MgW/sub 2/vacantO/sub 12/, Ba/sub 6/Ysub(2-x)REsub(x)/sup 3 +/W/sub 3/vacantO/sub 18/, and Sr/sub 8/SrGdsub(2-x)REsub(x)/sup 3 +/W/sub 4/vacantO/sub 24/

    Energy Technology Data Exchange (ETDEWEB)

    Kemmler-Sack, S [Tuebingen Univ. (Germany, F.R.). Lehrstuhl fuer Anorganische Chemie 2

    1981-12-01

    Rhombohedral 12 L staking polytypes Ba/sub 2/Lasub(2-x)REsub(x)/sup 3 +/MgW/sub 2/vacantO/sub 12/ show with RE/sup 3 +/ = Pr, Sm, Eu, Tb, Dy, Ho, Er, Tm; the 18 L stacking polytypes Ba/sub 6/Ysub(2-x)REsub(x)/sup 3 +/W/sub 3/vacantO/sub 18/ and the polymorphic perovskites Sr/sub 8/SrGdsub(2-x)REsub(x)/sup 3 +/W/sub 4/vacantO/sub 24/ with RE/sup 3 +/ = Sm, Eu, Dy, Ho, Er visible photoluminescence. The concentration dependence and the influence of the coordination number of the rare earth are reported.

  2. Separation and purification of Molybdenum-99 using the AG1x8 and Chelex-100 resins; Separacion y purificacion de Molibdeno-99 utilizando las resinas AG1x8 y Chelex-100

    Energy Technology Data Exchange (ETDEWEB)

    Sanchez M, V; Lopez C, R; Millan S, S; Fucugauchi, L A

    1991-05-15

    In the separation of the fission products of the molybdenum-99 soluble in watery solution of sodium hydroxide its have been used advantageously ion exchange processes with resins, which present a great stability toward the oxidizers and reducers agents as well as toward the ionizing radiation. The main stages of the recovery process of Mo-99 starting from the fission products of U-235 enriched. The first step of the purification is the elimination of the alumina taken place in the alkaline breakup of the badges of alloy uranium-aluminum. For it is used it a resin of anion exchange denominated AG1X8. The second stage of the consistent process in the elimination of the remaining fission products that accompany the one Mo-99, by means of the use of the exchange resin Chelex-100. Lastly is carried out the a sublimation process to obtain the pure Mo-99. (Author)

  3. Tests on the measurement of iodine-131 in milk using anionic ion-exchangers; Essais relatifs au dosage de l'iode 131 dans le lait au moyen d'echangeur d'ion anionique

    Energy Technology Data Exchange (ETDEWEB)

    Jeanmaire, L; Patti, F; Daburon, M L; Gros, R; Bertrand, S [Commissariat a l' Energie Atomique, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

    1966-07-01

    The milk produced by a cow contaminated by a single ingestion has been passed over a Dowex 1 resin to fix the iodine it contained, The percentage amount fixed, originally around 100 per cent, falls to 50 per cent after 15 days. (authors) [French] Le lait d'une vache contaminee par ingestion unique a ete passe sur resine Dowex 1 pour fixer l'iode qu'il contenait. Le pourcentage de fixation, qui a l'origine est voisin de 100 pour cent, tombe a 50 pour cent au bout de 15 jours. (auteurs)

  4. The isolation of lutetium from gadolinium contained in Purex process solutions

    International Nuclear Information System (INIS)

    Bostick, D.T.; Vick, D.O.; May, M.P.; Walker, R.L.

    1992-09-01

    A chemical separation procedure has been devised to isolate Lu from Purex dissolver solutions containing the neutron poison, Gd. The isolation procedure involves the removal of U and >Pu from a dissolver solution using tributylphosphate solvent extraction. If required, solvent extraction using di-(2-ethylhexyl) phosphoric acid can be employed to further purify the sample be removing alkali and alkali earth elements. Finally, Lu is chromatographically separated from Gd and rare earth fission products on a Dowex 50W-X8 resin column using an alpha-hydroxyisobutyrate eluant. The success of the chemical separation procedure has been demonstrated in the quantitative recovery of as little as 1.4 ng Lu from solutions containing a 5000-fold excess of Gd. Additionally, Lu has been isolated from synthetic dissolver samples containing U, Ba, Cs, and Gd. Thermal emission MS data indicated that the Lu fraction of the synthetic sample was free of Gd interference

  5. Feasibility studies for production of {sup 89}Sr in the Fast Breeder Test Reactor (FBTR)

    Energy Technology Data Exchange (ETDEWEB)

    Saha, Debasish; Vithya, J.; Ashok Kumar, G.V.S.; Swaminathan, K.; Kumar, R.; Venkata Subramani, C.R.; Vasudeva Rao, P.R. [Indira Gandhi Centre for Atomic Research (IGCAR), Kalpakkam (India). Fuel Chemistry Div.

    2013-07-01

    {sup 89}Sr, a pure beta emitter with half life of 50.53 d is used as its chloride solution for palliative care of bone metastases. This paper describes the feasibility studies that have been conducted at FBTR, IGCAR for production of this radionuclide using the {sup 89}Y(n, p){sup 89}Sr reaction. Yttria pellets were irradiated in a special subassembly at the core centre for a total of 73 d in two steps of 35 d and 38 d with a time gap of 38 d. The irradiated yttria target was dissolved in nitric acid and the bulk Y was separated by solvent extraction using the TBP-HNO{sub 3} complex. The {sup 89}Sr fraction was purified using the cation exchange resin DOWEX 50W x 8 (100-200 mesh size) from the other radioactive impurities seen. The eluted {sup 89}Sr fraction was assayed using a GM counting system. The {sup 89}Sr activity produced in 1 g of yttria pellet was found to be 19 mCi. (orig.)

  6. Capacity Enhancement for Hybrid Fiber-Wireless Channels with 46.8Gbit/sWireless Multi-CAP Transmission over 50m at W-Band

    DEFF Research Database (Denmark)

    Rommel, Simon; Puerta Ramírez, Rafael; Vegas Olmos, Juan José

    2017-01-01

    Transmission of a 46.8 Gbit/s multi-band CAP signal is experimentally demonstrated over a 50 m W-band radio-over-fiber link. Bit error rates below 3.8×10-3 are achieved, employing nine CAP bands with bit and power loading.......Transmission of a 46.8 Gbit/s multi-band CAP signal is experimentally demonstrated over a 50 m W-band radio-over-fiber link. Bit error rates below 3.8×10-3 are achieved, employing nine CAP bands with bit and power loading....

  7. Radiochemical study of Re/W adsorption behavior on a strongly basic anion exchange resin

    International Nuclear Information System (INIS)

    Gott, Matthew D.; Missouri Univ., Columbia, MO; Ballard, Beau D.; Redman, Lindsay N.

    2014-01-01

    Rhenium-186g is a radionuclide with a high potential for therapeutic applications. It emits therapeutic β - particles accompanied by low energy γ-rays, which allows for in-vivo tracking of the radiolabeled compound and dosimetry estimates. The current reactor production pathway 185 Re(n,γ) 186g Re produces low specific activity 186g Re, thereby limiting its therapeutic application. Work is underway to develop an accelerator-based, charged particle induced production method for high specific activity 186g Re from targets of enriched 186 W. To optimize the chemical 186g Re recovery method, batch studies have been performed to characterize the adsorption behavior of Re and W on a strongly basic anion exchange resin. An in-depth physicochemical profile was developed for the interaction of Re with resin material, which showed the reaction to be endothermic and spontaneous. Basic (NaOH) and acidic (HNO 3 ) matrices were used to determine the equilibrium distribution coefficients for Re and W. The resin exhibits the best affinity for Re at slightly basic conditions and little affinity above moderately acidic concentrations. Tungsten has low affinity for the resin above moderately basic concentrations. A study was performed to examine the effect of W concentration on Re adsorption, which showed that even a high ionic WO 4 2- strength of up to 1.9 mol kg -1 does not significantly compromise ReO 4 - retention on the resin. (orig.)

  8. Cation exchange resins labeled with holmium-166 for treatment of liver malignancy

    International Nuclear Information System (INIS)

    Costa, Renata F.; Osso Junior, Joao A.

    2008-01-01

    The increasing interest in new therapeutic radiopharmaceuticals is prompting investigators to utilize isotopes with more focused capabilities for treating various tumors, reducing the negative effects on neighboring healthy cells. Local radionuclide therapy using radioactive microspheres is a promising therapy for non-operable group of patients suffering from liver malignancies. Many publications have shown the success of this technique. The emphasis in the present work is the resin-based microspheres labeled with 166 Ho. The production of 166 Ho is feasible in the IEA-R1 Reactor at IPEN-CNEN/SP, because it does not need high power and high neutron fluxes. Samples of Ho 2 O 3 were irradiated in selected positions of the nuclear reactor IEA-R1 at IPEN/CNEN-SP. The neutron flux was 1.0 x10 13 n.s -1 .cm -2 for 1 hour. The dissolution of Ho 2 O 3 was studied with different volumes of 0.1M HCl and also varying the heating temperature. The AG50W-X8 200-400 mesh and CM Sephadex C-25 cation exchange resins were labeled with 166 Ho. The retention of 166 Ho in the resins was studied and also its stability. The results of the dissolution experiments of Ho 2 O 3 showed that there is a direct relation between the increasing volumes needed to dissolve higher masses, and also the positive effect of raising the temperature. The results show very good retention of 166 Ho in both columns, even when high volumes of 0.1M HCl are passed through the column containing the resins and its good stability towards saline solution, PBS solution and glucose.Although the resins employed in this work did not have the right particle size (20-50μm), the chemical behavior showed the very good labeling of the resins with 166 Ho, and its stability. (author)

  9. Development of chemical analysis techniques: pt. 3

    International Nuclear Information System (INIS)

    Kim, K.J.; Chi, K.Y.; Choi, G.C.

    1981-01-01

    For the purpose of determining trace rare earths a spectrofluorimetric method has been studied. Except Ce and Tb, the fluorescence intensities are not enough to allow satisfactory analysis. Complexing agents such as tungstate and hexafluoroacetylacetone should be employed to increase fluorescence intensities. As a preliminary experiment for the separation of individual rare earth element and uranium, the distribution coefficient, % S here, are obtained on the Dowex 50 W against HCl concentration by a batch method. These % S data are utilized to obtain elution curves. The % S data showed a minimum at around 4 M HCl. To understand this previously known phenomenon the adsorption of Cl - on Dowex 50 W is examined as a function of HCl concentration and found to be decreasing while % S of rare earths increasing. It is interpreted that Cl - and rare earth ions are moved into the resin phase separately and that the charge and the charge densities of these ions are responsible for the different % S curves. Dehydration appears to play an important role in the upturn of the % S curves at higher HCl concentrations

  10. Radiochemical study of Re/W adsorption behavior on a strongly basic anion exchange resin

    Energy Technology Data Exchange (ETDEWEB)

    Gott, Matthew D. [Los Alamos National Laboratory, Los Alamos, NM (United States). Chemistry Div.; Missouri Univ., Columbia, MO (United States). Dept. of Chemistry; Ballard, Beau D.; Redman, Lindsay N. [Los Alamos National Laboratory, Los Alamos, NM (United States). Chemistry Div.; and others

    2014-07-01

    Rhenium-186g is a radionuclide with a high potential for therapeutic applications. It emits therapeutic β{sup -} particles accompanied by low energy γ-rays, which allows for in-vivo tracking of the radiolabeled compound and dosimetry estimates. The current reactor production pathway {sup 185}Re(n,γ){sup 186g}Re produces low specific activity {sup 186g}Re, thereby limiting its therapeutic application. Work is underway to develop an accelerator-based, charged particle induced production method for high specific activity {sup 186g}Re from targets of enriched {sup 186}W. To optimize the chemical {sup 186g}Re recovery method, batch studies have been performed to characterize the adsorption behavior of Re and W on a strongly basic anion exchange resin. An in-depth physicochemical profile was developed for the interaction of Re with resin material, which showed the reaction to be endothermic and spontaneous. Basic (NaOH) and acidic (HNO{sub 3}) matrices were used to determine the equilibrium distribution coefficients for Re and W. The resin exhibits the best affinity for Re at slightly basic conditions and little affinity above moderately acidic concentrations. Tungsten has low affinity for the resin above moderately basic concentrations. A study was performed to examine the effect of W concentration on Re adsorption, which showed that even a high ionic WO{sub 4}{sup 2-} strength of up to 1.9 mol kg{sup -1} does not significantly compromise ReO{sub 4}{sup -} retention on the resin. (orig.)

  11. Immobilization of α-amylase and amyloglucosidase onto ion-exchange resin beads and hydrolysis of natural starch at high concentration.

    Science.gov (United States)

    Gupta, Kapish; Jana, Asim Kumar; Kumar, Sandeep; Maiti, Mithu

    2013-11-01

    α-Amylase was immobilized on Dowex MAC-3 with 88 % yield and amyloglucosidase on Amberlite IRA-400 ion-exchange resin beads with 54 % yield by adsorption process. Immobilized enzymes were characterized to measure the kinetic parameters and optimal operational parameters. Optimum substrate concentration and temperature were higher for immobilized enzymes. The thermal stability of the enzymes enhanced after the immobilization. Immobilized enzymes were used in the hydrolysis of the natural starch at high concentration (35 % w/v). The time required for liquefaction of starch to 10 dextrose equivalent (DE) and saccharification of liquefied starch to 96 DE increased. Immobilized enzymes showed the potential for use in starch hydrolysis as done in industry.

  12. Evaluation of new macroporous resins for the removal of uranium and plutonium from waste streams

    International Nuclear Information System (INIS)

    Koenst, J.W.; Herald, W.R.

    1976-01-01

    Organic ion exchange resins were evaluated for 238 Pu(IV), 238 Pu(VI), and 233 U(VI) removal from water. The capacity of the resins and equilibrium coefficients (Kd) were compared with each other and to bone char--an inorganic adsorbent consisting of hydroxyapatite (HAP) for which data is available. Bone char gave the best results for the removal of 238 Pu(IV), Amberlite XE279 (one of the new macroporous resins) gave the best results for 238 Pu(VI), and another macroporous resin, Dowex-MSA-1, gave good results for 233 U(VI). Kd values were shown to be a function of pH

  13. Determination of uranium concentrations and "2"3"4U/"2"3"8U activity ratio in some granitic rock samples by alpha spectrometry: application of a radiochemical procedure

    International Nuclear Information System (INIS)

    Khattab, Mahmoud R.

    2016-01-01

    The present study is an application of a radiochemical procedure using alpha spectrometry technique for determination of uranium isotopes "2"3"8U, "2"3"4U and "2"3"5U on 13 granitic samples. These samples were collected from Gabal Gattar area, Northeastern Desert, Egypt. The collected samples were digested using microwave technique with aqua regia and spiked with "2"3"2U for chemical yield and activity calculation. Separation of uranium isotopes from the samples was done by Dowex 1 x 4 (50-100 mesh) resin followed by source preparation using microprecipitation technique. The concentrations of "2"3"8U were ranged between 28.9±0.9 and 134.8±1.8 Bq/g, and the "2"3"4U concentrations were between 24±0.6 and 147.7±2.2 Bq/g. For the "2"3"5U, the activity concentrations were between 1.3±0.2 and 6.7±1.2 Bq/g. The activity ratio of "2"3"4U/"2"3"8U was calculated and varied from 0.80 to 1.30. (author)

  14. Superconducting single X-ray photon detector based on W0.8Si0.2

    Directory of Open Access Journals (Sweden)

    Xiaofu Zhang

    2016-11-01

    Full Text Available We fabricated a superconducting single X-ray photon detector based on W0.8Si0.2, and we characterized its basic detection performance for keV-photons at different temperatures. The detector has a critical temperature of 4.97 K, and it is able to be operated up to 4.8 K, just below the critical temperature. The detector starts to react to X-ray photons at relatively low bias currents, less than 1% of Ic at T = 1.8 K, and it shows a saturated count rate dependence on bias current at all temperatures, indicating that the optimum internal quantum efficiency can always be reached. Dark counts are negligible up to the highest investigated bias currents (99% of Ic and operating temperature (4.8 K. The latching effect affects the detector performance at all temperatures due to the fast recovery of the bias current; however, further modifications of the device geometry are expected to reduce the tendency for latching.

  15. Separation of macro-quantities of actinide elements at Savannah River by high-pressure cation exchange

    International Nuclear Information System (INIS)

    Burney, G.A.

    1980-01-01

    Large-scale separation of actinides from fission products and from each other by pressurized cation exchange chromatography at Savannah River is reviewed. Several kilograms of 244 Cm have been separated, with each run containing as much as 150 g of 244 Cm. Dowex 50W-X8 (Dow Chemical Co.) cation resin, graded to 30-70 micron size range, is used, and separation is made by eluting with 0.05M diethylenetriamine pentaacetic acid (DTPA) at a pH of 3. The effluent from the column is continuously monitored by a BF 3 detector, a NaI detector, and a lithium-drifted germanium detector and gamma spectrometer to guide collection of product fractions. Operating the columns at 300 to 1000 psi pressure eliminates resin bed disruption caused by radiolytically produced gases, and operating at increased flow rates decreases the radiolytic degradation of the resin per unit of product processed. A portion of the hot canyon of a production radiochemical separation plant was converted from a remote crane-operated facility to a master-slave manipulator-operated facility for separation and purification of actinide elements by pressurized cation exchange. It also contains an evaporator, furnaces, a calorimeter, and several precipitators and associated tanks. Actinide processing from target dissolution to packaging of purified product is planned in this facility

  16. Study and development recuperation of Thallium-203 from bombarded targets of this metal in production of Thallium-201 via addition of Thallium-201 radioisotope as a tracer

    International Nuclear Information System (INIS)

    Shirazi, B.

    2006-01-01

    Thallium-203 is the main material for 201 TlCl 3 radiopharmaceutical. It is very important to recover the remaining enriched Thallium-203 in every stage of the process to be reused in the production loop. In this research, the recuperation of Thallium-203 was studied with Dowex 508 ion exchange resin and Thallium-201 as a tracer. The results based on filling of ( 1 8 X 1.5) cm columns with this resin showed that the best flow rate of eluent is 2 ml/min. Also the most suitable volumes are 200 mL (HNO 3 0.05 M), 400 mL (solution of Thallium-203), 100 mL (H 2 O), 500 mL (Citric acid), 100 mL (H 2 0), 100 mL (EDTA 0.5 M and pH∼12.5). 60 mL (H 2 0), respectively

  17. EPICOR-II resin degradation results from first resin samples of PF-8 and PF-20

    International Nuclear Information System (INIS)

    McConnell, J.W. Jr.; Sanders, R.D. Sr.

    1985-12-01

    The 28 March 1979 accident at Three Mile Island Unit 2 released approximately 560,000 gallons of contaminated water to the Auxiliary and Fuel Handling Buildings. The water was decontaminated using a demineralization system called EPICOR-II developed by Epicor, Inc. The Low-Level Waste Data Base Development - EPICOR-II Resin/Liner Investigation Project is studying the chemical and physical conditions of the synthetic ion exchange resins found in several EPICOR-II prefilters. This report summarizes results and analyses of the first sampling of ion exchange resins from EPICOR-II prefilters PE-8 and -20. Results are compared with baseline data from tests performed on unirradiated Epicor, Inc. resins to determine if degradation has occurred due to the high internal radiation dose received by the EPICOR-II resins. Results also are compared with recent findings on resin degradation by Battelle Columbus Laboratories and Brookhaven National Laboratory. Analyses comparing test results of resins from EPICOR-II prefilters PF-8 and -20 with unirradiated resins obtained from Epicor, Inc. show resin degradation has occurred in some of the EPICOR-II resins examined. The mechanism of degradation is compared with work of other researchers and is consistent with their findings. The strong acid cation resins (divinylbenzene, styrene base structure) are losing effective cross-linking along with scission of functional groups and are experiencing first an increase and eventually a decrease in total exchange capacity as the absorbed radiation dose increases. The phenolic cation resins (phenol-formaldehyde base structure) show a loss of effective cross-linking and oxidation of the polymer chain. Analyses of resins removed from EPICOR-II prefilters PF-8 and -20 over the next several years should show a further increase in degradation

  18. Removal of aluminum(III)-based turbidity in water using hydrous titanium oxide dispersed in ion-exchange resins

    International Nuclear Information System (INIS)

    Venkataramani, B.; Karweer, S.B.; Iyer, R.K.; Phatak, G.M.; Iyer, R.M.

    1988-01-01

    An adsorber consisting of hydrous titanium oxide (HTiO) dispersed in a Dowex-type ion-exchange resin matrix (designated RT resins) has been developed which is capable of removing Al(III)-based colloidal dispersions in the neutral pH condition. The effect of resin crosslinking, particle size, HTiO loading, turbidity level, and flow rate on the turbidity removal efficiency of RT resins has been studied. It is demonstrated that a train of columns comprising RT resin, H + , and OH - form of resins could be used for large-scale purification operations at high flow rates. These columns, apart from removing turbidity and associated radioactivity, can effectively remove dissolved uranium present in ppb levels when used for water purification in nuclear reactors

  19. Separation of hafnium from zirconium in sulfuric acid solutions using pressurized ion exchange

    International Nuclear Information System (INIS)

    Hurst, F.J.

    1981-01-01

    High-resolution pressurized ion exchange has been used successfully to study and separate hafnium and zirconium sulfate complexes by chromatographic elution from Dowex 50W-X8 (15 to 25 μm) resin with sulfuric acid solutions. Techniques were developed to continuously monitor the column effluents for zirconium and hafnium by reaction with fluorometric and colorimetric reagents. Since neither reagent was specific for either metal ion, peak patterns were initially identified by using the stable isotopes 90 Zr and 180 Hf as fingerprints of their elution position. Distribution ratios for both zirconium and hafnium decrease as the inverse fourth power of the sulfuric acid concentration below 2N and as the inverse second power at higher acid concentration. The hafnium-to-zirconium separation factor is approximately constant (approx. 8) over the 0.5 to 3N range. Under certain conditions, an unseparated fraction was observed that was not retained by the resin. The amount of this fraction which is thought to be a polymeric hydrolysis product appears to be a function of metal and sulfuric acid concentrations. Conditions are being sought to give the highest zirconium concentration and the lowest acid concentration that can be used as a feed material for commercial scale-up in the continuous annular chromatographic (CAC) unit without formation of the polymer

  20. FIA versatile system for spectrophotometric determinations of vanadium and molybdenum exploring the catalytic activities of V(V) and Mo(VI); Sistema FIA polivalente para determinacoes espectrofotometricas de vanadio e molibdenio explorando as atividades cataliticas de V(V) e Mo(VI)

    Energy Technology Data Exchange (ETDEWEB)

    Luca, Gilmara Caseri de

    1996-02-01

    A versatile system for chemical analysis by flow injection analysis was developed and applied for catalytic spectrophotometric determination of vanadium or molybdenum in metallic alloys. The selected methods were based upon indicator reactions chromotropic (CS)-bromate acid or hydrogen iodide-peroxide, respectively. Initially, a model system was proposed, in which common parameters for methods were studied. This included a re-sampling process in which high degrees of samples dilution were obtained. Other parameters such as concentrations and reagents addition order, reaction medium Ph, temperature and ionic power, as well as procedures for sample solubilization, were studied relating to each method. A mini-column with cationic exchanger resin (Dowex 50W-X8, 50-100 mesh, H{sup +} form) was used. The system for vanadium determination processes 120 samples by hour, consuming 2,0 mg CS and 10 mg K Br O{sub 3b}y determination. Concerning the method for molybdenum, the reagents consumption was 2,0 mg KI and 1,0 {mu}L of solution 30% H{sub 2}O{sub 2} by determination, since the analytic velocity was the same, in relation to vanadium.

  1. Radiochemical determination of Beryllium-7 in a fission-product mixture containing many inorganic salts; Determination radiochimique du beryllium-7 dans un melange de produits de fission riche en sels mineraux

    Energy Technology Data Exchange (ETDEWEB)

    Prigent, Y; Van Kote, F [Commissariat a l' Energie Atomique, Bruyeres-le-Chatel (France). Centre d' Etudes

    1969-07-01

    A radiochemical method is described for analysing beryllium-7 in a mixture of fission products containing many inorganic salts. By studying the influence of various parameters it has been possible to speed up the decontamination on an anionic resin using an HCl isopropanol mixture, as proposed by KORKISCH- and al. Be(OH){sub 2} is first precipitated in the presence of E.D.T.A.; the main contaminants are then fixed on Dowex 1 x 10 in 12 M HCl and on Dowex 1 x 8 in a 3 M HCl (20 per cent)-isopropanol (80 per cent) (vol/vol) mixture. The Be, which is not fixed, is precipitated by NH{sub 4}H{sub 2}PO{sub 4} in the presence of E.D.T.A., ignited as Be{sub 2}P{sub 2}O{sub 7}, filtered, weighed, and analyzed by gamma spectrometry. The method makes it possible to dose 4 samples in 16 hours with a chemical yield of 80 per cent, using a 4 day-old fission product solution. The overall decontamination factor, exceeds 10{sup 8}. (authors) [French] On decrit un procede d'analyse radiochimique du beryllium-7 a partir d'un melange de produits de fission riche en sels mineraux. L'etude de l'influence de differents parametres a permis d'accelerer la decontamination sur resine anionique en milieu HCl-isopropanol proposee par KORKISCH et COLL. On precipite d'abord Be(OH){sub 2} en presence d'E.D.T.A., puis fixe les principaux contaminants sur Dowex 1 x 10 en milieu HCl 12 M et sur Dowex 1 x 8 en milieu HCl 3 M (20 pour cent)-isopropanol (80 pour cent) (v/v). Be, non fixe, est precipite par NH{sub 4}H{sub 2}PO{sub 4} en presence d'E.D.T.A., calcine en Be{sub 2}P{sub 2}O{sub 7}, filtre, pese et analyse par spectrometrie gamma. La methode permet de traiter quatre echantillons en 16 h, avec un rendement de 80 pour cent, a partir d'une solution de produits de fission vieille de quatre jours. Le facteur de decontamination global depasse 10{sup 8}. (auteurs)

  2. Separation of 99Mo from 132Te using thiourea as complexing agent. Application to the separation of 99Mo from the fission products

    International Nuclear Information System (INIS)

    Mestnik, S.A.C.; Silva, C.P.G. da.

    1989-02-01

    A radiochemical method to isolate 99 Mo from 132 Te both produced in the fission of 235 U has been developed. The methods is based on the formation of a cationic complex of tellerium with thiourea in acid medium which is retained (98.7 +- 0.5)% on a cation exchange resin (Dowex 50W-X8, 100 - 200 mesh) while (99.8 +- 0.05)% 99 Mo passes through it, due to the non formation of such complex in the same experimental conditions. The radionuclidic purity of the separated 99 Mo verified by using gamma spectrometry was found to be suitable for the preparation of 99 Mo - 99 sup (m)Tc generators. The retention of 99 Mo on an alumina column as function of ph was investigated. the best pH range for this purpose was found to be between 4.0 - 4.5. the 99 Mo - 99m Tc generator was prepared. the elution of 99m Tc was carried out with physiologic saline solution. The radionuclidic purity of the eluate was found suitable and the product can be used for Nuclear Medicine applications. (author) [pt

  3. Design, integration and demonstration of a 50 W JP8/kerosene fueled portable SOFC power generator

    Science.gov (United States)

    Cheekatamarla, Praveen K.; Finnerty, Caine M.; Robinson, Charles R.; Andrews, Stanley M.; Brodie, Jonathan A.; Lu, Y.; DeWald, Paul G.

    A man-portable solid oxide fuel cell (SOFC) system integrated with desulfurized JP8 partial oxidation (POX) reformer was demonstrated to supply a continuous power output of 50 W. This paper discusses some of the design paths chosen and challenges faced during the thermal integration of the stack and reformer in aiding the system startup and shutdown along with balance of plant and power management solutions. The package design, system capabilities, and test results of the prototype unit are presented.

  4. Neutron activation analysis of biological materials for sub PPM amount of mercury without determining the chemical yield

    International Nuclear Information System (INIS)

    Foldzinska, A.; Dybczynski, R.

    1976-01-01

    A simple method for the determination of sub ppm amounts of mercury in various biological materials by neutron activation analysis is described. Irradiated samples were decomposed with H 2 SO 4 - fuming HNO 3 mixture and mercury selectively isolated by ion exchange chromatography using Dowex 50X2(H + ) and Dowex 1X4(Br - ) columns in HBr medium. Finally the activity of 197 Hg fixed on an anion exchange resin was measured either with a Ge(Li) or a NaI (Tl) detector. Both the high radiochemical purity of mercury and the practically quantitative recovery were achieved thus eliminating the necessity of determining the chemical yield. The method was used for the determination of mercury in flour, milk, butter, margarine, fish, etc. Total time of analysis (including counting) amounted to 6-7 hrs and several samples could be simultaneously analysed by one technician. (T.G.)

  5. Screening Analyses of Pinosylvin Stilbenes, Resin Acids and Lignans in Norwegian Conifers

    OpenAIRE

    Anne Fiksdahl; Karin Oyaas; Ingebjorg Leirset; Hanne Hovelstad

    2006-01-01

    The content and distribution of stilbenes and resin acids in Scots pine (Pinus sylvestris) and spruce (Picea abies), sampled in central Norway, have been examined. The contents of pinosylvin stilbenes in pine heartwood/living knots were 0.2-2/2-8 % (w/w). No stilbenes could be detected in spruce (Picea abies). The resin acid contents of pine sapwood/heartwood and knots were 1-4 and 5-10 % (w/w), respectively. Minor amounts of resin acids (

  6. Crystalline-to-amorphous phase transformation in mechanically alloyed Fe50W50 powders

    International Nuclear Information System (INIS)

    Sherif El-Eskandarany, M.S.; Sumiyama, K.; Suzuki, K.

    1997-01-01

    A mechanical alloying process via a ball milling technique has been applied for preparing amorphous Fe 50 W 50 alloy powders. The results have shown that during the first and second stages of milling (0 to 360 ks) W atoms emigrate to Fe lattices to form nanocrystalline b.c.c. Fe-W solid solution, with a grain size of about 7 nm in diameter. After 720 ks of the milling time, this solid solution was transformed to an amorphous Fe-W alloy coexisting with the residual fraction of the unprocessed W powders. During the last stage of milling (720 to 1,440 ks) all of this residual W powder reacts with the amorphous phase to form a homogeneous Fe 50 W 50 amorphous alloy. The crystallization temperature and the enthalpy change of crystallization of amorphous Fe 50 W 50 powders milled for 1,440 ks were measured to be 860 K and -9kJ/mol, respectively. The amorphous Fe 50 W 50 powder produced is almost paramagnetic at room temperature. The powder comprises homogeneous and smooth spheres with an average size of about 0.5 microm in diameter

  7. Preparation of Zr(Mo,W)2O8 with a larger negative thermal expansion by controlling the thermal decomposition of Zr(Mo,W)2(OH,Cl)2∙2H2O.

    Science.gov (United States)

    Petrushina, Mariya Yu; Dedova, Elena S; Filatov, Eugeny Yu; Plyusnin, Pavel E; Korenev, Sergei V; Kulkov, Sergei N; Derevyannikova, Elizaveta A; Sharafutdinov, Marat R; Gubanov, Alexander I

    2018-03-28

    Solid solutions of Zr(Mo,W) 2 O 7 (OH,Cl) 2 ∙2H 2 O with a preset ratio of components were prepared by a hydrothermal method. The chemical composition of the solutions was determined by energy dispersive X-ray spectroscopy (EDX). For all the samples of ZrMo x W 2-x O 7 (OH,Cl) 2 ∙2H 2 O (x = 0.0, 0.2, 0.4, 0.6, 0.8, 1.0, 1.2, 1.4, 1.6, 1.8, and 2.0), TGA and in situ powder X-ray diffraction (PXRD) studies (300-1100 K) were conducted. For each case, the boundaries of the transformations were determined: Zr(Mo,W) 2 O 7 (OH,Cl) 2 ∙2H 2 O → orthorhombic-ZrMo x W 2-x O 8 (425-525 K), orthorhombic-ZrMo x W 2-x O 8  → cubic-ZrMo x W 2-x O 8 (700-850 K), cubic-ZrMo x W 2-x O 8  → trigonal-ZrMo x W 2-x O 8 (800-1050 K for x > 1) and cubic-ZrMo x W 2-x O 8  → oxides (1000-1075 K for x ≤ 1). The cell parameters of the disordered cubic-ZrMo x W 2-x O 8 (space group Pa-3) were measured within 300-900 K, and the thermal expansion coefficients were calculated: -3.5∙10 -6  - -4.5∙10 -6  K -1 . For the ordered ZrMo 1.8 W 0.2 O 8 (space group P2 1 3), a negative thermal expansion (NTE) coefficient -9.6∙10 -6  K -1 (300-400 K) was calculated. Orthorhombic-ZrW2O 8 is formed upon the decomposition of ZrW 2 O 7 (OH,Cl) 2 ∙2H 2 O within 500-800 K.

  8. Feasibility of isotachochromatography as a method for the preparative separation of weak acids and weak bases. II. Experimental verification

    NARCIS (Netherlands)

    Kooistra, C.; Sluyterman, L.A.A.E.

    1988-01-01

    The theory of isotachochromatography has been verified and proved to be essentially correct. Acetate was used as a leading buffer and mostly serine as a terminal buffer to separate acids with pKa values intermediate between those of the leading and terminal buffers on a column of Dowex 50W-X2.

  9. Neutrons at W 7-X

    Energy Technology Data Exchange (ETDEWEB)

    Junker, J.; Weller, A.

    1998-10-01

    The W 7-X deuterium plasma (18 MW NI, 4 keV, 1.5.10{sup 20} m{sup -3}) will produce 6.10{sup 16} neutrons during a 10 s pulse. A detailed geometrical model of the W 7-X experiment has been set up for the neutron transport calculations by the MCNP4B code (Monte Carlo neutron particle). The fast neutron flux (2.5 MeV) inside the torus is 100 times higher than inside the hall. The almost homogeneous thermal neutron flux inside the hall is reduced 30 times by doping the concrete walls with 700 ppm of boron. For a pulse scenario of 500 pulses per year the annual dose equivalent rate outside of the hall is down to the legally allowed level of 0.3 mSv/year, mainly by photons, due to the shielding of a 1.8 m thick concrete wall. The skyshine by the flux penetrating the 1.2 m thick concrete roof leads to 0.01 mSv/year at the fence. The structure of the experiment gets activated by the neutrons which for the chosen pulse scenario leads to a total activity varying between 2.6.10{sup 9} and 1.2.10{sup 13} Bq. The dominant isotopes are the superconductor compound ({sup 28}Al, {sup 66}Cu, {sup 94m}Nb) on the short timescale (min`s) and the steel components ({sup 51}Cr, {sup 54}Mn, {sup 60}Co) on the long timescale (months and years). For the austenitic steel a concentration of 50 ppm of Co has been assumed. After 10 years lifetime of the experiment it takes 4.8 years until the long living {sup 60}Co (T{sub 1/2} = 5.3 years) becomes the dominant radioactive isotope. Having waited for totally 10 years the specific activity has almost come down to 1.10{sup 5} Bq/to at which level a freely use of the material can be allowed.

  10. Edge modelling for W7-X

    International Nuclear Information System (INIS)

    Schneider, R.; Borchardt, M.; Riemann, J.; Bonnin, X.; Nuehrenberg, J.; Mutzke, A.

    2001-01-01

    The edge modelling activities for W7-X are summarized. The status of the new 3D SOL transport code BoRiS is presented, including an algorithm for calculation of magnetic coordinates and metric coefficients. In addition, the analysis of a toroidally averaged island topology with respect to the effect of drift and currents is discussed using the 2D B2-solps5.0 code. (author)

  11. Concentration of rhenium from dilute sodium chloride solutions

    Directory of Open Access Journals (Sweden)

    DRAGOLJUB M. LUKIC

    2008-03-01

    Full Text Available The conditions for the desorption of rhenium from the anion exchange resin Dowex 1-x8 by HNO3, HCl, H2SO4 and NaOH were determined. The solution (5.0´10-3 mol dm-3 Re in 0.15 mol dm-3 NaCl was passed through a column containing 0.10 g of the resin. The total sorbed amount of rhenium was 0.20 g/g of the resin. It was then eluted by the corresponding eluent in the concentration range up to about 3.0 mol dm-3. The highest elution efficiency and the most favourable elution profile were found with 3.0 mol dm-3 HNO3. Over 77 % of the sorbed rhenium was found in the first 5 ml of the eluate. Practically all the rhenium was recovered with 20 ml of the acid. Under the given experimental conditions, HCl and H2SO4 were less favourable while NaOH was not applicable, due to very low efficiency of rhenium elution.

  12. Resin purification from Dragons Blood by using sub critical solvent extraction method

    Science.gov (United States)

    Saifuddin; Nahar

    2018-04-01

    Jernang resin (dragon blood) is the world's most expensive sap. The resin obtained from jernang that grows only on the islands of Sumatra and Borneo. Jernang resin is in demand by the State of China, Hong Kong, and Singapore since they contain compounds that have the potential dracohordin as a medicinal ingredient in the biological and pharmacological activity such as antimicrobial, antiviral, antitumor and cytotoxic activity. The resin extracting process has conventionally been done by drizzly with maceration method as one way of processing jernang, which is done by people in Bireuen, Aceh. However, there are still significant obstacles, namely the quality of the yield that obtained lower than the jernang resin. The technological innovation carried out by forceful extraction process maceration by using methanol produced a yield that is higher than the extraction process maceration method carried out in Bireuen. Nevertheless, the use of methanol as a solvent would raise the production costs due to the price, which is relatively more expensive and non-environmentally friendly. To overcome the problem, this research proposed a process, which is known as subcritical solvent method. This process is cheap, and also abundant and environmentally friendly. The results show that the quality of jernang resins is better than the one that obtained by the processing group in Bireuen. The quality of the obtained jernang by maceration method is a class-A quality based on the quality specification requirements of jernang (SNI 1671: 2010) that has resin (b/b) 73%, water (w/w) of 6.8%, ash (w/b) 7%, impurity (w/w) 32%, the melting point of 88°C and red colours. While the two-stage treatment obtained a class between class-A and super quality, with the resin (b/b) 0.86%, water (w/w) of 6.5%, ash (w/w) of 2.8%, levels of impurities (w/w) of 9%, the melting point of 88 °C and dark-red colours.

  13. Blower Gun pellet injection system for W7-X

    Energy Technology Data Exchange (ETDEWEB)

    Dibon, M., E-mail: mathias.dibon@ipp.mpg.de [Max-Planck-Institute for Plasma Physics, Boltzmannstr. 2, 85748 Garching (Germany); Baldzuhn, J.; Beck, M. [Max-Planck-Institute for Plasma Physics, Boltzmannstr. 2, 85748 Garching (Germany); Cardella, A. [Lehrstuhl für Nukleartechnik, TU Munich, Boltzmannstr. 15, 85748 Garching (Germany); Köchl, F. [Atominstitut, TU Wien, 1020 Vienna (Austria); Kocsis, G. [Wigner RCP, RMI, P.O. Box 49, H-1525 Budapest-114 (Hungary); Lang, P.T. [Max-Planck-Institute for Plasma Physics, Boltzmannstr. 2, 85748 Garching (Germany); Macian-Juan, R. [Lehrstuhl für Nukleartechnik, TU Munich, Boltzmannstr. 15, 85748 Garching (Germany); Ploeckl, B. [Max-Planck-Institute for Plasma Physics, Boltzmannstr. 2, 85748 Garching (Germany); Szepesi, T. [Wigner RCP, RMI, P.O. Box 49, H-1525 Budapest-114 (Hungary); Weisbart, W. [Max-Planck-Institute for Plasma Physics, Boltzmannstr. 2, 85748 Garching (Germany)

    2015-10-15

    Highlights: • Operational principle of the ASDEX Upgrade Blower Gun. • Guiding tube properties for pellet guiding according to the requirements of W7-X. • Diagnostics for the characterization of the injection system. • Experimental procedure to investigate the performance of the Blower Gun. • Results concerning pellet speeds, mass loss, delivery efficiency and exit angle. - Abstract: Foreseen to perform pellet investigations in the new stellarator W7-X, the former ASDEX Upgrade Blower Gun was revised and revitalized. The systems operational characteristics have been surveyed in a test bed. The gun is designed to launch cylindrical pellets with 2 mm diameter and 2 mm length, produced from frozen deuterium D{sub 2}, hydrogen H{sub 2} or a gas mixture consisting of 50% H{sub 2} and 50% D{sub 2}. Pellets are accelerated by a short pulse of pressurized helium propellant gas to velocities in the range of 100–250 m/s. Delivery reliabilities at the launcher exit reach almost unity. The initial pellet mass is reduced to about 50% during the acceleration process. Pellet transfer to the plasma vessel was investigated by a first mock up guiding tube version. Transfer through this S-shaped stainless steel guiding tube (inner diameter 8 mm; length 6 m) containing two 1 m curvature radii was investigated for all pellet types. Tests were performed applying repetition rates from 2 Hz to 50 Hz and propellant gas pressures ranging from 0.1 to 0.6 MPa. For both H{sub 2} and D{sub 2}, low overall delivery efficiencies were observed at slow repetition rates, but stable efficiencies of about 90% above 10 Hz. About 10% of the mass is eroded while flying through the guiding tube. Pellets exit the guiding tube with an angular spread of less than 14°.

  14. Effect of light-curing units on the thermal expansion of resin nanocomposites.

    Science.gov (United States)

    Park, Jeong-Kil; Hur, Bock; Ko, Ching-Chang; García-Godoy, Franklin; Kim, Hyung-Il; Kwon, Yong Hoon

    2010-12-01

    To examine the thermal expansion of resin nanocomposites after light-curing using different light-curing units. Four different resin nanocomposites and four different light-curing units [quartz-tungsten-halogen (QTH), light emitting diode (LED), laser, and plasma arc] were chosen. Metal dies were filled with resin to make specimens and light-cured. The light intensity and light-curing time of the QTH and LED light-curing units were 1000 mW/cm2 and 40 seconds, 700 mW/cm2 and 40 seconds for the laser, and 1600 mW/cm2 and 3 seconds for the plasma arc. The coefficient of thermal expansion (CTE) was evaluated using a thermomechanical analyzer (TMA) at temperatures ranging from 30-80 degrees C. The CTE of the resin nanocomposites tested ranged from 28.5 to 65.8 (x 10(-6)/ degrees C), depending on the product and type of light-curing unit used. Among the specimens, Grandio showed the lowest CTE. The specimens cured using the plasma arc unit (Apollo 95E) showed the highest CTE. There was a linear correlation between the CTE and filler content (vol%) (R: -0.94-0.99 depending on the light-curing unit). The results may suggest a careful selection of the light-curing unit because there was more expansion in the specimens cured using the plasma arc unit than those cured by the other units.

  15. 1-Butanol absorption in poly(styrene-divinylbenzene) ion exchange resins for catalysis.

    Science.gov (United States)

    Pérez-Maciá, M A; Curcó, D; Bringué, R; Iborra, M; Rodríguez-Ropero, F; van der Vegt, N F A; Aleman, Carlos

    2015-12-21

    The swelling behaviour of poly(styrene-co-divinylbenzene), P(S-DVB), ion exchange resins in 1-butanol (BuOH) has been studied by means of atomistic classical molecular dynamics simulations (MD). The topological characteristics reported for the resin in the dry state, which exhibited complex internal loops (macropores), were considered for the starting models used to examine the swelling induced by BuOH contents ranging from 10% to 50% w/w. Experimental measurements using a laser diffraction particle size analyzer indicate that swelling causes a volume variation with respect to the dry resin of 21%. According to MD simulations, such a volume increment corresponds to a BuOH absorption of 31-32% w/w, which is in excellent agreement with the indirect experimental estimation (i.e. 31% w/w). Simulations reveal that, independently of the content of BuOH, the density of the swelled resin is higher than that of the dry resin, evidencing that the alcohol provokes important structural changes in the polymeric matrix. Thus, BuOH molecules cause a collapse of the resin macropores when the content of alcohol is ≤20% w/w. In contrast, when the concentration of BuOH is close to the experimental value (∼30% w/w), P(S-DVB) chains remain separated by pores faciliting the access of the reactants to the reaction centers. On the other hand, evaluation of both bonding and non-bonding interactions indicates that the mixing energy is the most important contribution to the absorption of BuOH into the P(S-DVB) resin. Overall, the results displayed in this work represent a starting point for the theoretical study of the catalytic conversion of BuOH into di-n-butyl ether in P(S-DVB) ion exchange resins using sophisticated electronic methods.

  16. Preparation of tritiated thymidine of high specific activity

    International Nuclear Information System (INIS)

    Ivan'kova, E.K.; Sidorov, G.V.; Myasoedov, N.F.

    1981-01-01

    Optimum conditions for the reaction are determined; and conditions for reaction component separation on resins of Dowex-1x8 and APA-8p (HCOO - , elution with ammonium formate) are optimized. It is established that the transition from thymine preparations with the specific activity of 0.15 and 1.5 TBq/mmol to the preparation with the specific activity of 3.25 TBq/mmol brings about the reduction in the desoxyribosylation reaction rate and the decrease in the thymidine yield from 85-90 to 65% [ru

  17. Fixation of metallic sulfosalicylate complexes on an anionic exchange resin

    International Nuclear Information System (INIS)

    Cahuzac, S.

    1969-06-01

    Since sulfosalicylate ions have acid-base properties, sulfosalicylate complexes have an apparent stability which varies with the ph. As a result, the fixation of sulfo-salicylates on an anionic exchange resin depends on the ph of the solution in equilibrium with the resin. This research has been aimed at studying the influence of the ph on the fixation on an anionic exchange resin (Dowex 1 x 4) of sulfosalicylate anions on the one hand, and of metallic sulfosalicylate complexes on the other hand. In the first part of this work, a determination has been made, by frontal analysis of the distribution of sulfosalicylate ions in the resin according to the total sulfosalicylate I concentration in the aqueous solution in equilibrium with the resin. The exchange constants of these ions between the resin and the solution have been calculated. In the second part, a study has been made of the fixation of anionic sulfosalicylate complexes of Fe(III), Al(III), Cr(III), Cu(II), Ni(II), Co(II), Zn(II), Mn(II), Cd(II), Fe(II) and UO 2 2+ . By measuring the partition coefficients of these different elements between the resin and the solution it has been possible to give interpretation for the modes of fixation of the metallic ions, and to calculate their exchange constant between the resin and the solution. The relationship has been established for each metallic element studied, between its partition coefficient, the ph and the total concentration of the complexing agent in solution. Such a relationship makes it possible to predict, for given conditions, the nature of the species in solution and in the resin, as well as the partition coefficient of a metallic, element. Finally, in the third part of the work, use has been made of results obtained previously, to carry out some separations (Ni 2+ - Co 2+ ; Ni 2+ - Co 2+ - Cu 2+ ; UO 2 2+ - Fe 3+ ; UO 2 2+ - Cr 3+ ; UO 2 2+ - Cu 2+ ; UO 2 2+ - Ni 2+ ; UO 2 2+ - Co 2+ ; UO 2 2+ - Mn 2+ and UO 2 2+ - Cd 2+ ), as well as the purification

  18. Non-hydrolytic sol-gel synthesis of epoxysilane-based inorganic-organic hybrid resins

    International Nuclear Information System (INIS)

    Jana, Sunirmal; Lim, Mi Ae; Baek, In Chan; Kim, Chang Hae; Seok, Sang Il

    2008-01-01

    A silica-based inorganic-organic hybrid resins (IOHR) were synthesized by non-hydrolytic sol-gel process from 3-glycidoxypropyltrimethoxysilane (GLYMO) and diphenylsilanediol (DPSD) at a fixed amount of (20 mol%) phenyltrimethoxysilane using barium hydroxide as a catalyst. The confirmation of condensation reaction in the IOHR was done by liquid state 29 Si NMR (Nuclear Magnetic Resonance) spectroscopy, measurement of viscosity as well as weight average molecular weight (W m ) of the IOHR. The W m of the IOHR was varied from 1091 to 2151, depending upon the DPSD content. Fourier transform infrared (FTIR) spectroscopic measurements were performed to investigate the details of vibrational absorption bands in the IOHR. It was seen that up to 50 mol% of DPSD there were no absorption peaks in the region of 3000-3600 cm -1 responsible for O-H groups and it reappeared at 60 mol% of DPSD due to some unreacted OH groups present in the resin. The IOHR at all the compositions was oily transparent liquid, miscible with various organic solvents like toluene, cyclohexanone, chloroform, tehrahydrofuran (THF), etc., and also commercial epoxy resins but immiscible with water. The color of the IOHR was pale yellow, which lightened with increasing DPSD content. The IOHR having 40-50 mol% of DPSD were storable. The refractive index at 632.8 nm of the resin films varied from 1.556 to 1.588, depending upon the resin composition. Physico-chemical properties such as the thermal stability, visible transparency, etc. after curing were investigated as a function of the chemical composition

  19. Avaliação in vitro da efetividade de polimerização da resina acrílica dental ativada através de energia de microondas, quando em contato com metal Use of microwave energy for processing acrylic resin near metal

    Directory of Open Access Journals (Sweden)

    Katia Olmedo BRAUN

    1998-04-01

    Full Text Available Com o objetivo de verificar a efetividade da energia de microondas na polimerização da resina acrílica próxima ao metal, foram confeccionados 36 corpos-de-prova cilíndricos com 30,0 mm de diâmetro x 4,0 mm de espessura, contendo no seu interior uma sela metálica com 28,0 mm x 8,0 mm x 0,5 mm, divididos aleatoriamente em 3 grupos e submetidos aos seguintes processamentos: G1 resina Clássico polimerizada em ciclo curto; G2 resina Acron-MC polimerizada em forno de microondas por 3 minutos a 500 W; G3 resina Clássico polimerizada em forno de microondas por 3 minutos a 500 W. Após a polimerização, cada amostra foi dividida em duas partes aproximadamente iguais, sendo que uma das partes foi utilizada para a avaliação de monômero residual, enquanto a outra foi submetida aos testes de dureza e porosidade. A dosagem de monômero liberada na água durante doze dias consecutivos foi avaliada através da espectrofotometria. A dureza Knoop foi verificada nas distâncias de 50, 100, 200, 400 e 800 mm da sela metálica, e a porosidade interna e externa foi avaliada a olho nu e com auxílio de microscópio com aumento de 100 X. Diante dos resultados obtidos, concluiu-se que a energia de microondas pode ser utilizada para a polimerização da resina acrílica contendo sela metálica no seu interior e que as resinas acrílicas convencionais, quando polimerizadas através da energia de microondas, apresentaram maior quantidade de poros.The conventional method to process acrylic resin is a time consuming step to construct removable prosthodontics. Microwave energy could provide a solution, but there are still questions regarding this process taking place in the presence of metal. The aim of this study was, therefore, to compare residual monomer, microhardness and porosity of two acrylic resins cured by different methods in the presence of a metal framework. The conditions evaluated were: Group 1 - Acrylic resin Clássico, short cycle heatcured for 3

  20. Neutral hydrogen in the neighborhood of the supernova remnant W 50

    International Nuclear Information System (INIS)

    Gosachinskii, I.V.; Khersonskii, V.K.

    1987-01-01

    Observations of neutral hydrogen at wavelength 21 cm in the neighborhood of the supernova remnant W 50, which contains the unique object SS 433, have been made with the RATAN-600 radio telescope with resolution 2' x 130' x 6.3 km/sec. At a radial velocity of about 34 km/sec (kinematic distance 3 kpc) a patchy HI cloud is found with outer diameter 65 pc and mass ∼ 3 x 10 4 M/sub circle/. In addition, at radial velocity 69 km/sec (kinematic distances 5.0 or 10.7 kpc) there is a HI cloud without appreciable large-scale motions. Some models that could explain the connection between these objects and the observed HI clouds are considered

  1. On grand unified SU(8)sub(L) x SU(8)sub(R) model

    International Nuclear Information System (INIS)

    Pirogov, Yu.F.

    1980-01-01

    In the model of early chiral grand unification SU(8)sub(L)xSU(8)sub(R) with intermediate symmetry hierarchies the radiation corrections for sinsup(2)thetasub(W)(μ) and α(μ) are calculated and unification mass M 8 is found in the one loop approximation with Higgs fields contribution being neglected. It is shown that there exists a natural hierarchy, leading to the decrease of sinsup(2)thetasub(W)(Msub(W)) down to the value sinsup(2)thetasub(W)=1/5-1/4 and simultaneous decrease of M 8 down to M 8 =(10 6 -10 7 ) GeV as compared with the values when there is no hierarchy [ru

  2. Radiochemical determination of Beryllium-7 in a fission-product mixture containing many inorganic salts

    International Nuclear Information System (INIS)

    Prigent, Y.; Van Kote, F.

    1969-01-01

    A radiochemical method is described for analysing beryllium-7 in a mixture of fission products containing many inorganic salts. By studying the influence of various parameters it has been possible to speed up the decontamination on an anionic resin using an HCl isopropanol mixture, as proposed by KORKISCH- and al. Be(OH) 2 is first precipitated in the presence of E.D.T.A.; the main contaminants are then fixed on Dowex 1 x 10 in 12 M HCl and on Dowex 1 x 8 in a 3 M HCl (20 per cent)-isopropanol (80 per cent) (vol/vol) mixture. The Be, which is not fixed, is precipitated by NH 4 H 2 PO 4 in the presence of E.D.T.A., ignited as Be 2 P 2 O 7 , filtered, weighed, and analyzed by gamma spectrometry. The method makes it possible to dose 4 samples in 16 hours with a chemical yield of 80 per cent, using a 4 day-old fission product solution. The overall decontamination factor, exceeds 10 8 . (authors) [fr

  3. X-1E launch from B-50 mothership

    Science.gov (United States)

    1950-01-01

    Beginning in 1946, two XS-1 experimental research aircraft (later redesignated X-1s) conducted pioneering tests at Muroc Army Air Field (now Edwards Air Force Base) in California to obtain flight data on conditions in the transonic speed range. These early tests culminated on October 14, 1947, in the first piloted flight faster than Mach 1.0, the speed of sound. During November, 1947, the Air Force authorized studies that led to a contract (W-33-038-ac-20062) with Bell Aircraft to build four (later three) improved X-1 aircraft (the X-1C being cancelled). Designated X-1A (#48-1384), X-1B (#48-1385), and X-1D (#48-1386), the airplanes were ready by late 1950. The aircraft were about five feet longer and 2,500 lbs. heavier than the original X-craft planes. They used the 8-percent wing like the earlier X-craft. The D-model had a low-pressure turbo-pump and the B model was fitted with a prototype hydrogen peroxide reaction control system for later aircraft to use in exoatmospheric research flights. Access was through a lift-off canopy. The planes were finished in their bare metal color and white. The X-1D was ready first, but on what was intended to be its second flight (August 22, 1951) it was jettisoned and crashed at Muroc after an aerial explosion while still mated to its mother (B-50A [#46-006A]) ship. The long-delayed X-1 #3 airplane with the turbine pump was finally completed for the NACA in 1951. It made its first glide flight on July 20, 1951, with NACA pilot Joseph Cannon. Its second and final captive flight was on November 9, 1951. It was destroyed on the ground by an explosion and fire along with its B-50A mother ship while attempting to jettison fuel. The X-1A arrived at Muroc in January, 1953 and had its first powered flight on February 21, 1953. On December 8, 1953 with Yeager as pilot, the aircraft investigated high-speed stability and control issues. The X-1A was turned over to the NACA, but was lost to aerial explosion on August 8, 1955, shortly before

  4. Study PWA8 resin for chromatographic uranium concentration

    International Nuclear Information System (INIS)

    Coceancigh, Herman; Ramella, J. L.; Marrero, Julieta; Jiménez Rebagliati, Raúl

    2013-01-01

    For many years nuclear industry have been using resins as filler of chromatographic columns. These methods are specific and give reliable results in different applications, for those reasons are extremely useful as separation process. Currently the nuclear industry is growing and this brings new issues such as the need of reduction of the amount of waste, the optimization of the production process and others that the chromatography could solve with great results. AMBERLITETM PWA8 resin is an anion exchange resin which can be used for the removal of uranium from drinking water. In addition to high exchange capacity, this resin has excellent physical stability and a wide range of pH in which is operational. With the idea of concentrating uranium from wastes solution as main goal we made different experiments to understand the AMBERLITETM PWA8 and obtain the most important characteristics like; pH working range; capacity; activation and elution procedures. These procedures were developed and optimized the capacity was determined using a batch experiment and we obtain that the maximum capacity is 882,5 U ug /resin gr at a pH of 4,2. Following on from these results chromatographic experiments were performed in which both were obtained the percentage of recovery and the concentration factor. The percent recovery (% R) calculated as the percentage ratio between the total mass and the load mass eluted (% R = eluted mass / total mass * 100) was 94% with a concentration factor of 5 times From these results it is intended to concentrate wastes solutions from the fuel cycle processes with two main goals: decreasing volume for storage and for future reusing of the uranium coming from production. (author)

  5. Transport modeling for W7-X on the basis of W7-AS experimental results

    International Nuclear Information System (INIS)

    Beidler, C.D.; Geiger, J.; Maassberg, H.; Marushchenko, N.B.; Turkin, Yu.

    2008-01-01

    Exploratory simulations of plasma confinement in the Wendelstein 7-X (W7-X) stellarator are presented, concentrating on scenarios which simultaneously achieve high temperature and high β (normalized plasma pressure) at the full magnetic field of B=2.5 T. Efficient 1-D transport and ray-tracing codes are combined to provide an approximately self-consistent description of the heating and current drive (ECCD) to be expected from up to 10 MW of electron cyclotron resonance heating (ECRH) in W7-X. Best performance is exhibited in high density (n=1.8x10 20 m -3 ) simulations heated at the second harmonic of the ordinary mode, although control of the magnetic topology at the plasma edge - needed to insure functioning of the island divertor - becomes problematic due to the imbalance of the bootstrap current and ECCD. (author)

  6. SuperLig® 639 Resin Performance using 8 Molar LAW Feed

    Energy Technology Data Exchange (ETDEWEB)

    Nash, C. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Williams, M. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Restivo, M. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Hamm, L. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); McCabe, D. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2016-01-15

    All prior testing with SuperLig® 639 has been done with the aqueous concentration of LAW at ~5 M [Na+], where the resin sinks, and can be used in a conventional down-flow column orientation. However, the aqueous LAW stream from the Waste Treatment Plant is expected to be ~8 M [Na+]. The resin would float in this higher density liquid, potentially disrupting the ability to achieve a good decontamination due to poor packing of the resin that leads to channeling. Testing was completed with a higher salt concentration in the feed simulant (7.8 M [Na+]) in an engineering-scale apparatus with two columns, each containing ~0.9 L of resin. Testing of this system used a simulant of the LAW solution, and substituted ReO4 - as a surrogate for TcO4 -. Results were then compared using computer modeling. Bench-scale testing was also performed, and examined an unconstrained resin bed, while engineering-scale tests used both constrained and unconstrained beds in a two-column, lead and lag sequential arrangement.

  7. SuperLig® 639 Resin Performance using 8 Molar LAW Feed

    International Nuclear Information System (INIS)

    Nash, C.; Williams, M.; Restivo, M.; Hamm, L.; McCabe, D.

    2016-01-01

    All prior testing with SuperLig® 639 has been done with the aqueous concentration of LAW at ~5 M [Na+], where the resin sinks, and can be used in a conventional down-flow column orientation. However, the aqueous LAW stream from the Waste Treatment Plant is expected to be ~8 M [Na+]. The resin would float in this higher density liquid, potentially disrupting the ability to achieve a good decontamination due to poor packing of the resin that leads to channeling. Testing was completed with a higher salt concentration in the feed simulant (7.8 M [Na+]) in an engineering-scale apparatus with two columns, each containing ~0.9 L of resin. Testing of this system used a simulant of the LAW solution, and substituted ReO4 - as a surrogate for TcO4 -. Results were then compared using computer modeling. Bench-scale testing was also performed, and examined an unconstrained resin bed, while engineering-scale tests used both constrained and unconstrained beds in a two-column, lead and lag sequential arrangement.

  8. Badania populacji Wielkopolski w zakresie 17 markerów Y-STRs oraz 8 Y-SNPs

    Directory of Open Access Journals (Sweden)

    Monica Abreu-Głowacka

    2014-10-01

    Full Text Available Celem pracy było określenie zróżnicowania genetycznego populacji Wielkopolski w zakresie 17 loci Y-STR i 8 loci Y-SNP oraz porównanie z populacją polską i innymi wybranymi populacjami. Badano 201  niespokrewnionych mężczyzn z regionu województwa wielkopolskiego. Uzyskano 184 pojedyncze haplotypy w zakresie 17 Y-STR, co dało siłę dyskryminacji 0.96. Najczęściej występujący haplotyp, Ht-50 zaobserwowano w 3 próbach, natomiast 7 różnych haplotypów zauważono podwójnie w analizowanej populacji. Tę samą grupę badawczą poddano analizie z wykorzystaniem 8 markerów Y-SNPs. Uzyskano 40 różnych haplotypów z siłą dyskryminacji wynoszącą 0.20. Najczęściej występujący haplotyp zaobserwowano u 38 mężczyzn. Uzyskane haplotypy zostały przypisane do 4 następujących haplogrup: K=19%, IJ=7%, R1a1=59% i R1b=15%. Wartość wskaźnika polimorfizmu genomowego dla badanych loci Y-SNP/Y-STR wyniosła 0,9883.

  9. Burnout experiments with 6 x 6, 8 x 8 and 7 x 7 rod bundle test sections using freon as model fluid

    International Nuclear Information System (INIS)

    Fulfs, H.; Katsaounis, A.; Minden, C.v.

    1976-01-01

    This paper reports on burnout experiments at staedy state condition using Freon12 as model fluid. The experiments were carried out with three test sections with 6 x 6, 8 x 8 and 7 x 7 rod bundles. The axial flux distribution of the rods is either constant or reactor like. The transformed measured points using STEVENS and BOURE scaling factors to equivalent water conditions respectively, were compared to the burnout correlation W3 using the reactor layout program DYNAMIT. The DYNAMIT code is a thermohydraulic lay-out reactor program without consideration of mixing flow between the subchannels. (orig.) [de

  10. Study of Ti4+ substitution in ZrW2O8 negative thermal expansion materials

    International Nuclear Information System (INIS)

    Buysser, Klaartje de; Driessche, Isabel van; Putte, Bart van de; Schaubroeck, Joseph; Hoste, Serge

    2007-01-01

    Powder XRD-analysis and thermo-mechanical analysis on sintered TiO 2 -WO 3 -ZrO 2 mixtures revealed the formation of Zr 1-x Ti x W 2 O 8 solid solutions. A noticeable decrease in unit cell parameter 'a' and in the order-disorder transition temperature could be seen in the case of Zr 1-x Ti x W 2 O 8 solid solutions. Studies performed on other ZrW 2 O 8 solid solutions have attributed an increase in phase transition temperature to a decrease in free lattice volume, whereas a decrease in phase transition temperature was suggested to be due to the presence of a more disordered state. Our studies indicate that the phase transition temperature in our materials is strongly influenced by the bond dissociation energy of the substituting ion-oxygen bond. A decrease in bond strength may compensate for the effect of a decrease in lattice free volume, lowering the phase transition temperature as the degree of substitution by Ti 4+ increases. This hypothesis is proved by differential scanning calorimetry. - Graphical abstract: This study indicates that the phase transition temperature in our materials Zr 1-x Ti x W 2 O 8 is strongly influenced by the bond dissociation energy of the substituting ion-oxygen bond. A decrease in bond strength may compensate for the effect of a decrease in lattice-free volume, lowering the phase transition temperature

  11. Ion exchange separation of carrier-free 140Ba and 140La from their equilibrium mixture using nitrilotriacetic acid and ascorbic acid as eluents

    International Nuclear Information System (INIS)

    Das, N.R.; Bhattacharyya, S.N.

    1982-01-01

    A simple cation exchange procedure for separation of 140 Ba- 140 La using Dowex 50W-X8 and nitrilotriacetic acid or ascorbic acid as the eluent has been described. The optimal separation of the daughter from the parent has been achieved using a 4% Na-nitrilotriacetate or Na-ascorbate solution at pH 7. The parent, 140 Ba, left in the column can be eluted with dilute hydrochloric acid or it can be retained in the column for milking off the daughter, 140 La, when needed. The radiochemical purity of the separated isotopes, 140 Ba and 140 La, were verified by γ-ray spectrometry. (author)

  12. W-reactivation of phage lambda in X-irradiated mutants of Escherichia coli K-12

    Energy Technology Data Exchange (ETDEWEB)

    Martignoni, K D; Haselbacher, I [Muenchen Univ. (Germany, F.R.). Strahlenbiologisches Inst.

    1980-07-01

    The survival of UV irradiated phage lambda was increased on X-irradiated E.coli K-12 host cells over that on unirradiated cells. The frequency of c mutants among the surviving phages was increased to a similar extent by the X-ray exposure of the host cells as by UV light. This W-reactivation of phage lambda occurred in uvrA, polA, and recB mutants besides the wild type at about equal X-ray doses, but at a reduced reactivation efficiency compared with the wild type. W-reactivation was undetectable in recA mutants. While maximal UV induced W-reactivation occured 30 min after irradiation, the maximal X-ray induced reactivation was found immediately after irradiation. Chloramphenicol (100 ..mu..g/ml) and nitrofurantoin (50 ..mu..g/ml) inhibited W-reactivation of phage lambda if added before irradiation of the host cells, indicating the necessity of protein synthesis for W-reactivation.

  13. Overview on W VII-X

    International Nuclear Information System (INIS)

    Wobig, H.

    1988-01-01

    Configurations for the W VII-X stellarator are reviewed. The MHD analysis of the Helias configuration with four field periods previously considered shows that the ballooning mode limit of the maximum plasma pressure increases with increasing number of field periods. Interest is focused on five-period Helias configurations with ballooning mode limits around a Beta factor of 5 %. Four configurations are discussed: HS4-12, an improved version of HS4-8; HS5-6, based on a quasi-helical equilibrium; plus two slightly different configurations designated as HS5-7 and HS5-8. It is proposed to increase the dimensions of the whole experiment to R=6.5m and to reduce the magnetic field to B=3T on the axis

  14. Fractionation of nitrogen and carbon isotopes by means of urea chromatography

    International Nuclear Information System (INIS)

    Hirschberg, K.; Krumbiegel, P.; Faust, H.

    1981-01-01

    Between aqueous urea solutions and strongly acid cation exchange resins of the polystyrene-sulfoacid type a solid-liquid-phase distribution equilibrium develops with an isotope effect of nitrogen and carbon in urea. The [ 13 C, 15 N] urea molecules are preferably bound to the exchanger matrix. The elementary separation factors for 15 N and 13 C enrichment have been determined to be 1.00 per cent. Column chromatographic separation with the aid of Dowex 50 WX8 renders the preparation of double-labelled urea feasible. (author)

  15. Purification and Pore Forming Activity of Two Hydrophobic Polypeptides from the Secretion of the Red Sea Moses Sole (Pardachirus marmoratus)

    Science.gov (United States)

    1986-11-01

    Uppsala, Sweden. Ovalbumin, bovine albumin fractio n V, soybean lecithin , sodium cnolate, gramicidin D and Dowex 50 x 8 (50-100 mesh) were obtained from...A-,.ino acid analysis 50 ug duplIcate samples of PXI and PXII, from reverse phase HPLC, were dissolved in 0.4 ml of 6 N HCI and hydrolyzed ocr 24 hr

  16. Resistive ballooning modes in W7-AS and W7-X

    International Nuclear Information System (INIS)

    Kaiser, R.

    1993-01-01

    'Critical' pressure gradients due to resistive ballooning modes and their growth rates were computed for the W7-AS stellarator and for a HELIAS configuration with W7-X parameters, and the two configurations were compared. The results are based on the evaluation of a fourth order magnetic differential equation along closed magnetic field lines. The numerical procedure applying a variational approach uses the 'Garching resistive ballooning code', GARBO, which was originally developed for the stability analysis of axisymmetric plasmas. Concerning purely growing modes, this analysis shows that the favourable stability properties of W7-X, already optimized with respect to ideal ballooning modes, persist in the resistive regime: the destabilizing effect of resistivity is largely compensated by the stabilizing contribution of plasma compression. As a consequence, the ideal β limit continues only moderately shifted in the resistive case and likewise ideal ballooning stable equilibria (up to β 0 ≅ 5%) do not become resistively unstable. The situation is different for W7-AS. Greater resistive effects (in comparison with W7-X) are found in a configuration that is already ideally much more unstable. A basic feature in resistive calculations is the occurrence of overstable modes. These modes no longer show a stability threshold and, for realistic values of pressure and resistivity, linear instability is obtained for W7-AS as well as for W7-X, with growth rates and oscillation frequencies in the kilo-Hertz range. (author). 29 refs, 13 figs

  17. Preparation and characterization of silane-modified SiO2 particles reinforced resin composites with fluorinated acrylate polymer.

    Science.gov (United States)

    Liu, Xue; Wang, Zengyao; Zhao, Chengji; Bu, Wenhuan; Na, Hui

    2018-04-01

    A series of fluorinated dental resin composites were prepared with two kinds of SiO 2 particles. Bis-GMA (bisphenol A-glycerolate dimethacrylate)/4-TF-PQEA (fluorinated acrylate monomer)/TEGDMA (triethylene glycol dimethacrylate) (40/30/30, wt/wt/wt) was introduced as resin matrix. SiO 2 nanopartices (30nm) and SiO 2 microparticles (0.3µm) were silanized with 3-methacryloxypropyl trimethoxysilane (γ-MPS) and used as fillers. After mixing the resin matrix with 0%, 10%, 20%, 30% SiO 2 nanopartices and 0%, 10%, 20%, 30%, 40%, 50% SiO 2 microparticles, respectively, the fluorinated resin composites were obtained. Properties including double bond conversion (DC), polymerization shrinkage (PS), water sorption (W p ), water solubility (W y ), mechanical properties and cytotoxicity were investigated in comparison with those of neat resin system. The results showed that, filler particles could improve the overall performance of resin composites, particularly in improving mechanical properties and reducing PS of composites along with the addition of filler loading. Compared to resin composites containing SiO 2 microparticles, SiO 2 nanoparticles resin composites had higher DC, higher mechanical properties, lower PS and lower W p under the same filler content. Especially, 50% SiO 2 microparticles reinforced resins exhibited the best flexural strength (104.04 ± 7.40MPa), flexural modulus (5.62 ± 0.16GPa), vickers microhardness (37.34 ± 1.13 HV), compressive strength (301.54 ± 5.66MPa) and the lowest polymerization (3.42 ± 0.22%). Copyright © 2018 Elsevier Ltd. All rights reserved.

  18. Determination of mercury in food by neutron activation

    International Nuclear Information System (INIS)

    Anand, S.J.S.

    1976-01-01

    Determination of mercury in food samples has been carried out by neutron activation followed by chemical separation to remove the interfering activities of copper, zinc etc. Chemical separation was carried out using anion exchange resin (DOWEX 1x8). Mercury was determined by counting 77 keV γ-rays of 197 Hg on a NaI(Tl) crystal in conjunction with a 400-channel pulse-height analyser. Levels of mercury in the following foods are tabulated: rice, wheat, pulses, millets, leafy vegetables, flower, carrot, potato, tomato, onion, chilli powder, sugar, tea leaves, milk. (T.I.)

  19. A production method for Cr-51 at IEN's cyclotron

    International Nuclear Information System (INIS)

    Bastos, M.A.V.; Britto, J.L.Q. de; Vinagre, U.M.; Silva, A.G. da.

    1989-01-01

    Thick target yields for the reactions 51 V(p,n) 51 Cr and 51 V(d,2n) 51 Cr were measured and compared with literature values. The excitation function for the 51 V(p,n) 51 Cr reaction was also measured. A method for the production and separation of this radioisotope was developed via the 51 V(p,n) 51 Cr reaction and a combination of Fe +3 co-precipitation and an anion exchange technique using a Dowex 1x8(100-200 mesh) resin in hydrochloric acid medium [pt

  20. Determination of mercury in food by neutron activation

    Energy Technology Data Exchange (ETDEWEB)

    Anand, S J.S. [Bhabha Atomic Research Centre, Bombay (India). Air Monitoring Section

    1976-01-01

    Determination of mercury in food samples has been carried out by neutron activation followed by chemical separation to remove the interfering activities of copper, zinc etc. Chemical separation was carried out using anion exchange resin (DOWEX 1x8). Mercury was determined by counting 77 keV ..gamma..-rays of /sup 197/Hg on a NaI(Tl) crystal in conjunction with a 400-channel pulse-height analyser. Levels of mercury in the following foods are tabulated: rice, wheat, pulses, millets, leafy vegetables, flower, carrot, potato, tomato, onion, chilli powder, sugar, tea leaves, milk.

  1. W/SiC X-ray multilayers optimized for use above 100 keV

    DEFF Research Database (Denmark)

    Windt, D.L.; Dongey, S.; Hailey, C.J.

    2002-01-01

    -derived optical constants, which we determined from reflectance-vs-incidence angle measurements also made using synchrotron radiation, in the range E=120 - 180 keV. We describe our experimental investigation in detail, compare the new W/SiC multilayers with both W/Si and W/B4C films that have been studied......We have developed a new depth-graded multilayer system comprising W and SiC layers, suitable for use as hard X-ray reflective coatings operating in the energy range 100 - 200 keV. Grazing incidence X-ray reflectance at E=8 keV was used to characterize the interface widths, as well as the temporal...... and thermal stability in both periodic and depth-graded W/SiC structures, while synchrotron radiation was used to measure the hard X-ray reflectance of a depth-graded multilayer designed specifically for use in the range Esimilar to150 - 170 keV. We have modeled the hard X-ray reflectance using newly...

  2. W/SiC x-ray multilayers optimized for use above 100 keV

    DEFF Research Database (Denmark)

    Windt, D.L.; Donguy, S.; Hailey, C.J.

    2003-01-01

    optical constants, which we determined from reflectance versus incidence angle measurements also made using synchrotron radiation, in the range E = 120-180 keV. We describe our experimental investigation in detail, compare the new W/SiC multilayers with both W/Si and W/B4C films that have been studied......We have developed a new depth-graded multilayer system comprising W and SiC layers, suitable for use as hard x-ray reflective coatings operating in the energy range 100-200 keV. Grazing-incidence x-ray reflectance at E = 8 keV was used to characterize the interface widths, as well as the temporal...... and thermal stability in both periodic and depth-graded W/SiC structures, whereas synchrotron radiation was used to measure the hard x-ray reflectance of a depth-graded multilayer designed specifically for use in, the range Esimilar to150-170 keV. We have modeled the hard x-ray reflectance using newly derived...

  3. Overview on W7-AS results with relevance for Wendelstein 7-X and the low-shear stellarator line

    International Nuclear Information System (INIS)

    Wagner, F.; Anton, M.; Baldzuhn, J.

    1999-01-01

    The Wendelstein stellarator programme of Garching has developed low shear stellarators with successively optimised designs to remove the intrinsic deficiencies of this 3D concept. W7-X, presently under construction, is in internal terminology a fully optimised stellarator. W7-AS, the presently operated device, is a partly optimised stellarator. The optimisation of stellarators aims at improved neoclassical confinement in the long mean free path regime and improved equilibrium and stability properties. In this report, we address equilibrium, stability, turbulent and collisional energy confinement aspects (role of magnetic shear, role of the radial electric field, low and improved confinement regimes), particle transport, transport and turbulence at the plasma edge, high density operation, ECRH (OXB scheme) and ICRF heating and the development of the island divertor for exhaust. The maximal parameters achieved in W7-AS (at different discharge types) are: T e = 5.8 keV, T i = 1.5 keV, n e = 3 x 10 20 m -3 , = 2%, τ E = 50 ms. (author)

  4. Overview on W7-AS results with relevance for WENDELSTEIN 7-X and the low-shear stellarator line

    International Nuclear Information System (INIS)

    Wagner, F.; Anton, M.; Baldzuhn, J.

    2001-01-01

    The Wendelstein stellarator programme of Garching has developed low shear stellarators with successively optimised designs to remove the intrinsic deficiencies of this 3D concept. W7-X, presently under construction, is in internal terminology a fully optimised stellarator. W7-AS, the presently operated device, is a partly optimised stellarator. The optimisation of stellarators aims at improved neoclassical confinement in the long mean free path regime and improved equilibrium and stability properties. In this report, we address equilibrium, stability, turbulent and collisional energy confinement aspects (role of magnetic shear, role of the radial electric field, low and improved confinement regimes), particle transport, transport and turbulence at the plasma edge, high density operation, ECRH (OXB scheme) and ICRF heating and the development of the island divertor for exhaust. The maximal parameters achieved in W7-AS (at different discharge types) are: T e = 5.8 keV, T i = 1.5 keV, n e = 3x10 20 m -3 , = 2%, τ E = 50 ms. (author)

  5. Production of no carrier added residue free /sup 22/Na

    Energy Technology Data Exchange (ETDEWEB)

    Britto, J L.Q. de; Bastos, M A.V.; Silva, R.F. da; Silva, A.G. da

    1988-05-02

    A method for the production of no carrier added and residue free /sup 22/Na, was developed via the /sup 24/Mg(d,..cap alpha..)/sup 22/Na nuclear reaction applying 14 MeV deuterons and a high current MG-Cu target. The yield for the reaction was measured and the chemical separation was performed using a Dowex 50WX8 resin in H/sup +/ form. The overall yield was higher than 98%. Residue could not be detected. All experiments were carried out at IEN's CV-28 cyclotron. (author) 13 refs.; 2 figs.

  6. Transmission of broad W/Rh and W/Al (target/filter) x-ray beams operated at 25-49 kVp through common shielding materials.

    Science.gov (United States)

    Li, Xinhua; Zhang, Da; Liu, Bob

    2012-07-01

    To provide transmission data for broad 25-39 kVp (kilovolt peak) W/Rh and 25-49 kVp W/Al (target/filter, W-tungsten, Rh-rhodium, and Al-aluminum) x-ray beams through common shielding materials, such as lead, concrete, gypsum wallboard, wood, steel, and plate glass. The unfiltered W-target x-ray spectra measured on a Selenia Dimensions system (Hologic Inc., Bedford, MA) set at 20-49 kVp were, respectively, filtered using 50-μm Rh and 700-μm Al, and were subsequently used for Monte Carlo calculations. The transmission of broad x-ray beams through shielding materials was simulated using Geant4 low energy electromagnetic physics package with photon- and electron-processes above 250 eV, including photoelectric effect, Compton scattering, and Rayleigh scattering. The calculated transmission data were fitted using Archer equation with a robust fitting algorithm. The transmission of broad x-ray beams through the above-mentioned shielding materials was calculated down to about 10(-5) for 25-39 kVp W/Rh and 25-49 kVp W/Al. The fitted results of α, β, and γ in Archer equation were provided. The α values of kVp ≥ 40 were approximately consistent with those of NCRP Report No. 147. These data provide inputs for the shielding designs of x-ray imaging facilities with W-anode x-ray beams, such as from Selenia Dimensions.

  7. Separation of rare earths from solutions of phosphoric acid

    International Nuclear Information System (INIS)

    Jones, E.A.

    1977-01-01

    Rare earths are separated from 6M phosphoric acid by adsorption onto cation resin BIORAD AG50W-X8. The phosphoric acid is then washed from the column, and the rare earths are eluted with 4M hydrochloric acid

  8. Designs of Langmuir probes for W7-X

    International Nuclear Information System (INIS)

    Laube, Ralph; Laux, Michael; Ye, Min You; Greuner, Henri; Lindig, Stefan

    2011-01-01

    Several designs of Langmuir probes for the stellarator Wendelstein 7-X (W7-X) are described. Different types of probes are proposed for the different divertors to be used during different operational phases of W7-X. Comb-like arrays of stiff probes, arrays of flexible probes, and fixed inlay probes are reviewed. For the initial phase of W7-X it was decided to install arrays of fixed inlay probes. Two mockups were manufactured and one of them was tested with success in the high heat flux test facility GLADIS. For long-pulse operation of W7-X different conceptual designs are proposed and are still developed further. This paper summarizes the different design constrains for the Langmuir probes in the different divertor surroundings, describes the design of the array of inlay probes for the initial phase and the result of the GLADIS test, and gives a preview of the conceptual designs of probes for the long-pulse operational phase of W7-X.

  9. ECRH and W7-X: An intriguing pair

    Science.gov (United States)

    Erckmann, V.; Braune, H.; Gantenbein, G.; Jelonnek, J.; Kasparek, W.; Laqua, H. P.; Lechte, C.; Marushchenko, N. B.; Michel, G.; Plaum, B.; Thumm, M.; Weissgerber, M.; Wolf, R.; W7-X ECRH Teams

    2014-02-01

    The construction of the W7-X basic machine is almost completed and the device is approaching the commissioning phase. W7-X operation will be supported by ECRH working at 140 GHz in 2nd harmonic X- or O-mode with 10 MW cw power. Presently the activities at W7-X concentrate on the implementation of wall-armour, in-vessel components and diagnostics. The ECRH-system is in stand by with 5 out of 10 gyrotrons operational. The status of both, the W7-X device and the ECRH system is reported. Further R&D activities concentrate on extending the launching capability for sophisticated confinement investigations with remote steering launchers in a poloidal plane with weak magnetic field gradient.

  10. Determination of microquantities of zirconium and thorium in uranium dioxide

    International Nuclear Information System (INIS)

    Weber de D'Alessio, Ana; Zucal, Raquel.

    1975-07-01

    A method for the determination of 10 to 50 ppm of zirconium and thorium in uranium IV oxide of nuclear purity is established. Zirconium and thorium are retained in a strong cation-exchange resin Dowex 50 WX8 in 1 M HCl. Zirconium is eluted with 0,5% oxalic acid solution and thorium with 4% ammonium oxalate. The colorimetric determination of zirconium with xilenol orange is done in perchloric acid after destructtion of oxalic acid and thorium is determined with arsenazo III in 5 M HCl. 10 μg of each element were determined with a standard deviation of 2,1% for thorium and 3,4% for zirconium. (author) [es

  11. Determination of radionuclide levels in rainwater using ion exchange resin and γ-spectrometry

    International Nuclear Information System (INIS)

    Jungck, Matthias H.A.; Andrey, Jean-Louis; Froidevaux, Pascal

    2009-01-01

    The evaluation of radioactivity accidentally released into the atmosphere involves determining the radioactivity levels of rainwater samples. Rainwater scavenges atmospheric airborne radioactivity in such a way that surface contamination can be deduced from rainfall rate and rainwater radioactivity content. For this purpose, rainwater is usually collected in large surface collectors and then measured by γ-spectrometry after such treatments as evaporation or iron hydroxide precipitation. We found that collectors can be adapted to accept large surface (diameter 47 mm) cartridges containing a strongly acidic resin (Dowex AG 88) which is able to quantitatively extract radioactivity from rainwater, even during heavy rainfall. The resin can then be measured by γ-spectrometry. The detection limit is 0.1 Bq per sample of resin (80 g) for 137 Cs. Natural 7 Be and 210 Pb can also be measured and the activity ratio of both radionuclides is comparable with those obtained through iron hydroxide precipitation and air filter measurements. Occasionally 22 Na has also been measured above the detection limit. A comparison between the evaporation method and the resin method demonstrated that 2/3 of 7 Be can be lost during the evaporation process. The resin method is simple and highly efficient at extracting radioactivity. Because of these great advantages, we anticipate it could replace former rainwater determination methods. Moreover, it does not necessitate the transportation of large rainwater volumes to the laboratory

  12. Three rapid methods for determination {sup 90}Sr in milk samples using liquid scintillation spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Abbasisiara, F.; Attarilar, N. [Iranian Nuclear Regulatory Authority (INRA), Atomic Energy Organization of Iran (AEOI), Environmental Radiation Protection Div., National Radiation Protection Dept. (Iran, Islamic Republic of); Afshar, N. [Tarbiat Modarres Univ. (Iran, Islamic Republic of)

    2006-07-01

    Strontium radionuclide {sup 90}Sr is one of the main long-lived components of the radioactive fallout which occurred as a result of previous atmospheric nuclear tests and also nuclear accidents such as Chernobyl accident. Due to chemical and biochemical similarities between strontium and calcium, more than 99% of strontium is efficiently incorporated into bone tissue and teeth and Characterized by along physical and biological half-life, it may cause damage to bone marrow. Since determination of this radionuclide often is a time consuming process, rapid determination methods specially in emergency situations is always desirable. In this work, three rapid methods for determination of this radionuclide in milk samples will be evaluated. All of the methods include two major steps: 1- strontium separation from fats and proteins which can be performed by drying (in case of the fresh milk samples), ashing and leaching by nitric acids or by using exchange or chelating resins which have strong affinity for alkaline earth cations such as Dowex 50W-X8. And 2- Separation of Sr-90 or its daughter product, Y-90. In two methods separation of {sup 90}Sr is performed by extraction of the daughter nuclide, {sup 90}Y, by aid of organic extracting agent, Tributylphosphate or T.B.P., and then Cherenkov counting of the Y-90 extracted. The third method is based on separation of this radionuclide using Crown Ether or Sr -Spec resin. The detailed radiochemical procedures and evaluation of each method advantages or disadvantages will explained in full text paper. (authors)

  13. Three rapid methods for determination 90Sr in milk samples using liquid scintillation spectrometry

    International Nuclear Information System (INIS)

    Abbasisiara, F.; Attarilar, N.; Afshar, N.

    2006-01-01

    Strontium radionuclide 90 Sr is one of the main long-lived components of the radioactive fallout which occurred as a result of previous atmospheric nuclear tests and also nuclear accidents such as Chernobyl accident. Due to chemical and biochemical similarities between strontium and calcium, more than 99% of strontium is efficiently incorporated into bone tissue and teeth and Characterized by along physical and biological half-life, it may cause damage to bone marrow. Since determination of this radionuclide often is a time consuming process, rapid determination methods specially in emergency situations is always desirable. In this work, three rapid methods for determination of this radionuclide in milk samples will be evaluated. All of the methods include two major steps: 1- strontium separation from fats and proteins which can be performed by drying (in case of the fresh milk samples), ashing and leaching by nitric acids or by using exchange or chelating resins which have strong affinity for alkaline earth cations such as Dowex 50W-X8. And 2- Separation of Sr-90 or its daughter product, Y-90. In two methods separation of 90 Sr is performed by extraction of the daughter nuclide, 90 Y, by aid of organic extracting agent, Tributylphosphate or T.B.P., and then Cherenkov counting of the Y-90 extracted. The third method is based on separation of this radionuclide using Crown Ether or Sr -Spec resin. The detailed radiochemical procedures and evaluation of each method advantages or disadvantages will explained in full text paper. (authors)

  14. Improvement in char formability of phenolic resin for development of Carbon/Carbon composites

    International Nuclear Information System (INIS)

    Hajhosseini, M.; Payami, A.; Ghaffarian, S. R.; Rezadoust, A. M.

    2008-01-01

    In the processing of carbon/carbon composites using polymer resin as the matrix precursor, it is inevitable that a porous structure was formed after carbonization. As a result, densification by liquid phase impregnation followed by recarbonization is required to obtain a densified composite. Consequently, the char formability of resin is an important factor in reducing the number of densification cycles and hence the processing cost. In this study, a novel approach is adopted to improve the densification of carbon/carbon composites by using a new phenolic resin modified by pitch. For this purpose, soluble part of pitch was extracted and dispersed in resol type phenolic resin. The polymerization reaction was performed in presence of para-formaldehyde and a resol-pitch compound was obtained. The second compound was prepared by mixing novolac-furfural in 55:45 weight ratio containing 9% by weight hexamethylene tetramine. This compound was added to resol-pitch compound in 10,20,50 and 80 w %. The microstructure of carbonized resin was investigated by X-ray diffraction and char yield, and the linear and volumetric shrinkage were obtained. Results show that in 80:20 ratio of resol-pitch to novolac-furfural , the char yield would be maximized by 71% and volumetric shrinkage would be minimized at 16.4%. At the same time, XRD results indicate that the resin has a strong ability to graphitize carbon/carbon composites matrix as a necessary step for its processing

  15. A novel method for selective separation of {sup 111}In from impurities by ion exchange chromatography

    Energy Technology Data Exchange (ETDEWEB)

    Yavari, R.; Khanachi, A.R.; Ghannad Maragheh, M.; Bagheri, G. [Jaber Ibn-e Hayan Research Laboratories, A.E.O.I., Tehran (Iran)

    2004-07-01

    {sup 111}In is one of the most important cyclotron-produced radionuclides that is prepared from nuclear reactions like Cd (p,xn){sup 111}In and Cd (d,xn) {sup 111}In. It is used in various branches of medicine such as lymphoscintigraphy and cisternography. Several methods have been reported in the literature for the separation of carrier-free {sup 111}In from irradiated cadmium matrix. But there has not been a sufficiently fast method for this purpose until recently. In this work, a new method has been developed for the separation of {sup 111}In from a cadmium target by using Dowex 50W-X8 as an ion exchanger. (orig.)

  16. Effect of two lasers on the polymerization of composite resins: single vs combination.

    Science.gov (United States)

    Ro, Jung-Hoon; Son, Sung-Ae; Park, Jeong-kil; Jeon, Gye-Rok; Ko, Ching-Chang; Kwon, Yong Hoon

    2015-07-01

    The selection of a light-curing unit for the curing composite resins is important to achieve best outcomes. The purpose of the present study was to test lasers of 457 and 473 nm alone or in combination under different light conditions with respect to the cure of composite resins. Four different composite resins were light cured using five different laser combinations (530 mW/cm(2) 457 nm only, 530 mW/cm(2) 473 nm only, 177 mW/cm(2) 457 + 177 mW/cm(2) 473 nm, 265 mW/cm(2) 457 + 265 mW/cm(2) 473 nm, and 354 mW/cm(2) 457 + 354 mW/cm(2) 473 nm). Microhardness and polymerization shrinkage were evaluated. A light-emitting diode (LED) unit was used for comparison purposes. On top surfaces, after aging for 24 h, microhardness achieved using the LED unit and the lasers with different conditions ranged 42.4-65.5 and 38.9-67.7 Hv, respectively, and on bottom surfaces, corresponding ranges were 25.2-56.1 and 18.5-55.7 Hv, respectively. Of the conditions used, 354 mW/cm(2) 457 nm + 354 mW/cm(2) 473 nm produced the highest bottom microhardness (33.8-55.6 Hv). On top and bottom surfaces, microhardness by the lowest total light intensity, 354 (177 × 2) mW/cm(2), ranged 39.0-60.5 and 18.5-52.8 Hv, respectively. Generally, 530 mW/cm(2) at 457 nm produced the lowest polymerization shrinkage. However, shrinkage values obtained using all five laser conditions were similar. The study shows the lasers of 457 and 473 nm are useful for curing composite resins alone or in combination at much lower light intensities than the LED unit.

  17. Design, performance, and economics of 50-kW and 500-kW vertical axis wind turbines

    Science.gov (United States)

    Schienbein, L. A.; Malcolm, D. J.

    1983-11-01

    A review of the development and performance of the DAF Indal 50-kW vertical axis Darrieus wind turbine shows that a high level of technical development and reliability has been achieved. Features of the drive train, braking and control systems are discussed and performance details are presented. Details are also presented of a 500-kW VAWT that is currently in production. A discussion of the economics of both the 50-kW and 500-kW VAWTs is included, showing the effects of charge rate, installed cost, operating cost, performance, and efficiency.

  18. A production method for Cr-51 at IEN's cyclotron

    Energy Technology Data Exchange (ETDEWEB)

    Bastos, M A.V.; Britto, J L.Q. de; Vinagre, U M; Silva, A.G. da [Universidade Federal, Rio de Janeiro, RJ (Brazil). Coordenacao dos Programas de Pos-graduacao de Engenharia

    1990-01-01

    Thick target yields for the reactions {sup 51} V(p,n){sup 51} Cr and {sup 51} V(d, 2 n){sup 51} Cr were measured and compared with literature values. The excitation function for the {sup 51} V(p,n){sup 51} Cr reaction was also measured. A method for the production and separation of this radioisotope was developed via the {sup 51} V(p,n){sup 51} Cr reaction and a combination of Fe+3 coprecipitation and an anion exchange technique using a Dowex 1X8(100-200 mesh) resin in hydrochloric acid medium. (author).

  19. A production method for Cr-51 at IEN's cyclotron

    Energy Technology Data Exchange (ETDEWEB)

    Bastos, M A.V.; Britto, J L.Q. de; Vinagre, U M; Silva, A.G. da [Instituto de Engenharia Nuclear, Rio de Janeiro (Brazil). Dept. de Fisica

    1990-01-01

    Thick target yields for the reactions {sup 51}V(p,n){sup 51}Cr and {sup 51}V(d,2n){sup 51}Cr were measured and compared with literature values. The excitation function for the {sup 51}V(p,n){sup 51}Cr reaction was also measured. A method for the production and separation of this radioisotope was developed via the {sup 51}V(p,n){sup 51}Cr reaction and a combination of Fe{sup +3} coprecipitation and an anion exchange technique using a Dowex 1X8 (100-200 mesh) resin in hydrochloric acid medium. (orig.).

  20. Mercury determination in natural waters using neutron activation analysis

    International Nuclear Information System (INIS)

    Cagnone, M.; Marques, R.O.

    1994-01-01

    Available as short communication only. An analytical method for quantitative determination of Mercury traces in river and sea water is proposed. The neutron activation method and radiochemical separation of Mercury by developing of C L 4 Hg -2 complex, and their chromatographic separation using anionic exchange resin Dowex 1 X 8 of 400 mesh is used. The quantitative determination is done by gamma spectrometric analysis. The selection limits reached with this method showed that this is an amenable procedure in routine mercury determination in the ppb level, specially useful in the environmental contamination analysis. (author). 3 refs, 2 figs, 1 tab

  1. The influence of "C-factor" and light activation technique on polymerization contraction forces of resin composite

    Directory of Open Access Journals (Sweden)

    Sérgio Kiyoshi Ishikiriama

    2012-12-01

    Full Text Available OBJECTIVES: This study evaluated the influence of the cavity configuration factor ("C-Factor" and light activation technique on polymerization contraction forces of a Bis-GMA-based composite resin (Charisma, Heraeus Kulzer. MATERIAL AND METHODS: Three different pairs of steel moving bases were connected to a universal testing machine (emic DL 500: groups A and B - 2x2 mm (CF=0.33, groups C and D - 3x2 mm (CF=0.66, groups e and F - 6x2 mm (CF=1.5. After adjustment of the height between the pair of bases so that the resin had a volume of 12 mm³ in all groups, the material was inserted and polymerized by two different methods: pulse delay (100 mW/cm² for 5 s, 40 s interval, 600 mW/cm² for 20 s and continuous pulse (600 mW/cm² for 20 s. Each configuration was light cured with both techniques. Tensions generated during polymerization were recorded by 120 s. The values were expressed in curves (Force(N x Time(s and averages compared by statistical analysis (ANOVA and Tukey's test, p<0.05. RESULTS: For the 2x2 and 3x2 bases, with a reduced C-Factor, significant differences were found between the light curing methods. For 6x2 base, with high C-Factor, the light curing method did not influence the contraction forces of the composite resin. CONCLUSIONS: Pulse delay technique can determine less stress on tooth/restoration interface of adhesive restorations only when a reduced C-Factor is present.

  2. First results on the sorption behaviour of Rutherfordium from HCl/HF containing aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Schumann, D.; Nitsche, H. [Technische Univ. Dresden (Germany); Taut, S. [Forschungszentrum Rossendorf e.V. (FZR), Dresden (Germany); Jost, D.T.; Gaeggeler, H.W. [Paul Scherrer Inst. (PSI), Villigen (Switzerland); Yakushev, A.B.; Buklanov, G.V.; Domanov, V.P.; Lien Din Thi [Joint Inst. for Nuclear Research, Dubna (Russian Federation); Kubica, B.; Misiak, R.; Szeglowski, Z. [NINP Cracow (Poland)

    1997-09-01

    Rutherfordium shows strong sorption on the cation exchanger DOWEX 50x8 at a concentration of 0.1 M HCl/10{sup -2} M HF. This shows that Rf behaves under these conditions differently from Hf and Zr and more like Th under these conditions. (author) 1 fig., 5 refs.

  3. Results from X-ray measurements on the Wendelstein W7-AS stellarator

    Energy Technology Data Exchange (ETDEWEB)

    Weller, A; Brakel, R; Burhenn, R; Hacker, H; Lazaros, A [Max-Planck-Institut fuer Plasmaphysik, Garching (Germany, F.R.)

    1990-01-01

    X-ray imaging measurements have contributed to studies of the plasma equilibrium, plasma fluctuations, impurity radiation and impurity transport effects in the advanced stellarator Wendelstein W7-AS (R=2 m, a=17 cm). In addition, time resolved electron temperature profiles are deduced from X-ray intensity ratios according to the two absorber foil method. The plasma is generated and heated by fundamental and 2{sup nd} harmonic ECRH (P{le}800 kW at 70 GHz). Neutral beam injection heating (P{le}1.5 MW) was applied also, assisted by D{sub 2} pellet injection. (author) 8 refs., 7 figs.

  4. Initial operation of the CW 8X H- ion source discharge

    International Nuclear Information System (INIS)

    Smith, H.V. Jr.; Allison, P.; Geisik, C.; Schmitt, D.R.; Schneider, J.D.; Stelzer, J.E.

    1993-01-01

    A pulsed 8X source was built and the H - beam current, emittance, and power efficiency were measured. These results were promising, so a cooled, dc version designed for operation at arc power levels up to 30 kW was built. Testing of the CW 8X source discharge is underway. The design dc power loading on the cathode surface is 900 W/cm 2 , considerably higher than achieved in any previous Penning surface-plasma source (SPS). Thus, the electrode surfaces are cooled with pressurized, hot water. The authors describe the source and present the initial operating experience and arc test results

  5. The management of spent resins at rad waste installation (RWI)

    International Nuclear Information System (INIS)

    Johan, Bahdir

    2002-01-01

    During years 2000 RWI has been managed 1.596 liters the spent resins from MPR, multipurpose reactor G.A. Siwabessy (RSG-GAS). The spent resins containing 6 0 C o, 1 37 C s and 8 9 S r. The immobilization of spent resins using Portland cement type I and sand in shell 950 liter has been carried out. The immobilization product quality was characterized by measurement of surface exposure, density, compression strength and leaching rate. The samples each being 3000 g are made by taking cement slurry from the 950 liter shell. The samples are molded in the form of cylinder of 50 mm diameter and height 50 mm. The density was determined by weighing and measuring sample's volume. The compression strength was determinate using P aul Weber a pparatus. The leaching rate by immerse of the samples in the demineralized water and the rate the contact surface dose measures using survey meter. The results show that the density ρ= (1,72 ± 0,01) s/d 1,73 ± 0,03) g.cm - 3 , the compression strength Γ= (20,10 ± 0,02 s/d 20,18 ± 0,02) N.mm - 2 , the leaching rate R n = (1,32x10 - 2 s /d 2,0x10 - 3 ) g.cm - 2 . h - 1 , the contact surface rate D 0 = (0,374 s/d 0,79) mrem.jam - 1 a nd 1m distance from the surface D 1 = (0,18 s/d 0,19) mrem.jam - 1 h ave been in compliance with the criteria recommended by IAEA the quality of spent resins concrete in shell 950 liters (number 22C to 27C) is qualified for ultimate disposal

  6. Symmetry hierarchies and radiative corrections in the grand unified model SU(8)/sub L/ x SU(8)/sub R/

    International Nuclear Information System (INIS)

    Pirogov, Y.F.

    1982-01-01

    In the SU(8)/sub L/ x SU(8)/sub R/ model of precocious chiral unification, radiative corrections for the effective parameters sin 2 theta/sub W/(μ) and α(μ) are calculated in the one-loop approximation, neglecting contributions of the Higgs fields, and the unification mass M 8 is determined in the presence of a hierarchy of intermediate symmetries. It is shown that a natural hierarchy exists which leads to a decrease in sin 2 theta/sub W/(M/sub W/L) down to the value sin 2 theta/sub W/ = (1/5)--(1/4) together with a decrease in M 8 down to M 8 = 10 6 --10 7 GeV in comparison with the values in the absence of a hierarchy

  7. 50 W Resonant SMPS with coreless transformer for AM radio application

    DEFF Research Database (Denmark)

    Nakhost, Pezhman; Munk-Nielsen, Stig

    2006-01-01

    Resonant converters are attractive in some applications, because of their soft-switching behaviour. The very low switching losses make them superior compared to traditional hard-switching converters. The present paper considers a 50 W resonant SMPS with coreless transformer for AM radio applicati......Resonant converters are attractive in some applications, because of their soft-switching behaviour. The very low switching losses make them superior compared to traditional hard-switching converters. The present paper considers a 50 W resonant SMPS with coreless transformer for AM radio...... percent deviation. The experimental tests show that the realized converter has a high performance and efficiency up to 87.6%. It is shown that with a DC input voltage range of 276-375 V, the output voltage is 15 V from 10 W to 50 W output power, except in no load. The output voltage ripple is 84 m......Vppand 114 mVppat 15 W and 50 W output power, respectively. In addition, ra switching frequency from 1.9 MHz up to around 4 MHz is possible....

  8. Separations chemistry

    International Nuclear Information System (INIS)

    Anon.

    1977-01-01

    Infrared spectra of Pu(IV) polymer show effects of CO 2 adsorption and of aging. Uv light (300 nm) increases the rate of reduction of PuO 2 2+ and Pu 4+ to Pu 3+ and the Pu--U separation factor using TBP. Distribution ratios for Zr and Hf between Dowex 50W--X8 resin and H 2 SO 4 solutions were found to decrease sharply with H 2 SO 4 content. Octylphenyl acid phosphate, a mixture of monooctylphenyl and dioctylphenyl phosphoric acids, is being studied for U recovery from wet-process phosphoric acid. A study of HNO 3 leaching of Ra from U ores was completed. Effects of particle size of the packed bed on the dispersion of the boundary of the miscible phase used in oil recovery are being studied. Effects of sulfonates on toluene--n-butanol--water phase relations were determined, as were the effects of salts and solutes on the max water content of 1:1 toluene--alcohol solutions. A study was begun of hydrocarbon solubility in water--surfactant--alcohol. The mechanism of the formation of hydrous ZrO 2 --polyacrylate membranes and their use for sulfate rejection were studied. Salt rejection through hyperfiltration by clay membranes (bentonite and kaolin) was also investigated. Preliminary results are given for hyperfiltration of wood-pulping wastes by ZrO 2 membranes. 13 figures

  9. The determination of radioactive strontium in environmental samples by preferential ion exchange separation from calcium

    International Nuclear Information System (INIS)

    Fukushima, Hiroto; Nonaka, Nobuhiro; Honda, Tetsutaro; Kimura, Toshimasa; Higuchi, Hideo

    1979-01-01

    The determination of radioactive strontium in environmental samples involves a difficulty in the separation and purification of strontium from large amounts of calcium. The principal technique employed in this study is based on a cation exchange separation after preferential chelation of calcium over strontium by EDTA. The alkaline earth fraction separated from samples is dissolved in 1.2 M HCl and an equivalent amount of EDTA is added. The solution is passed through a Dowex 50W-X8 ion exchange column at a flow rate of 20 ml/min after the pH has been adjusted to 5.1. A fraction of calcium retained on the resin is eluted out with 1.8 l of 2 w/v% EDTA solution at pH 5.1. Then the strontium is eluted with 450 ml of 2 M HCl. The strontium carbonate is precipitated, and the chemical yield is determined. After standing for 14 days to reach the radioactive equilibrium of 90 Sr - 90 Y, the activity of 89 Sr + 90 Sr + 90 Y is measured. Then the activity of 90 Sr + 90 Y is measured by milking the 90 Y. The proposed procedure has been applied to sea water, soil and various ash samples of vegetables, seaweeds and daily foods. The results obtained are in good agreement with those by a classical fuming nitric acid precipitation method. The detection limits are 0.1 pCi/l for 10 l of sea water, 10 pCi/kg for 100 g of soil and 1 pCi/kg-fresh for 20 g ash samples, respectively. (author)

  10. Neutral transport calculations for W VII-X. First applications to W VII-X

    International Nuclear Information System (INIS)

    Sardei, F.

    1988-01-01

    Results of neutral gas transport calculations obtained with the DEGAS code are presented for a W VII-AS model plasma and a source of neutrals due to limiter recycling. For typical profiles of the plasma parameters as predicted for an ECRH discharge, the simulation yields a radial drop of the average neutral population by a factor of 30. The neutrals are strongly localized near the limiter and have a poloidal minimum at its opposite side. For a W VII-X configuration (HS4-12), a neutral source given by a high recycling ion flux equally distributed over the wall is considered. For an ion density of 5 x 10 1 3 /cc and 30 eV edge temperature, the neutrals originating from the wall completely ionize within the ergodic region. The corresponding average energy of cx neutrals hitting the wall is less than 30 eV. Neutral penetration into the plasma locally depends on the distance between wall and separatrix

  11. Evaluation of ABS resin disk certified reference materials for heavy metal analysis by x-ray fluorescence analysis

    International Nuclear Information System (INIS)

    Ohata, Masaki; Kidokoro, Toshihiro; Kurahashi, Masayasu; Hioki, Akiharu

    2010-01-01

    ABS resin disk certified reference materials (CRMs) for heavy-metal analysis (NMIJ CRM 8105-a, NMIJ CRM 8106-a, NMIJ CRM 8115-a and NMIJ CRM 8116-a) were evaluated using an energy dispersive X-ray fluorescence (ED-XRF) analysis. The homogeneities of elements for both among-disks and within-disk were evaluated by ED-XRF analysis without any sample pre-treatment, which were similar to those evaluated by ICP-MS analysis after a sample digenstion procedure. The normalized XRF sensitivities for Cd, Cr and Pb in different ABS resin disk CRMs were compared, and the differences among them for those ABS resin disks that have similar matrices were observed. Moreover, Hg in those ABS resin disk CRMs was stable for long-term X-ray irradiation during ED-XRF analysis. (author)

  12. Study of the separation of metallic compounds by means of an anion exchanger resin and of complexing media

    International Nuclear Information System (INIS)

    Denis de Trobriand, Anne

    1971-01-01

    In order to define better separation conditions of molybdenum and aluminium from uranium alloys, this research thesis first reports the study of the fixation of each of these elements on a Dowex resin in a carbonate medium. Results obtained by other studies in a hydrogen carbonate medium has leaded to the use of mixing of CO 3 2- and HCO 3 - . In a last part, the author reports the analysis of two samples (uranium-molybdenum and uranium-aluminium): after an attack of these alloys in a melt carbonate medium, components are separated by elution in one of the studied media

  13. Ra/Ca separation by ion exchange chromatography

    International Nuclear Information System (INIS)

    Flores Mendoza, J.

    1990-01-01

    Ra/Ca separation by ion exchange. The objective of this work was to acquire knowledge of the chromatographic behaviour of the alkaline earth cations calcium, barium and radium and the obtention of well-defined alpha spectra of 226 Ra. Three cationic ion exchange resins (Dower 50 W-X8, AG 50W-XB and Merck I) and three complexing agents (ethylenediaminetetraacetic acid, citric acid and tartaric acid) at various pH values have been investigated. The three types of ions are fixed on the resins at pH 4.8; calcium is eluted at pH between 5 and 6 depending on the resin; barium and radium are eluted at pH values from 8 to 11. Radium is also eluted with a 2 M nitric acid solution, from which it can be electrodeposited on a stainless steel disk potassium fluoride as electrolyte at pH 14. The electrolysis is conducted for 18 hours with a current of mA. Under these conditions high resolution alpha spectra were obtained for 226 Ra, which was practically free from radioactive contaminants (Author)

  14. Immobilization of spent resin with epoxy resin

    International Nuclear Information System (INIS)

    Gultom, O.; Suryanto; Sayogo; Ramdan

    1997-01-01

    immobilization of spent resin using epoxy resin has been conducted. The spent resin was mixtured with epoxy resin in variation of concentration, i.e., 30, 40, 50, 60, 70 weight percent of spent resin. The mixture were pour into the plastic tube, with a diameter of 40 mm and height of 40 mm. The density, compressive strength and leaching rate were respectively measured by quanta chrome, paul weber apparatus and gamma spectrometer. The results showed that the increasing of waste concentration would be decreased the compressive strength, and increased density by immobilized waste. The leaching rate of 137 Cs from waste product was not detected in experiment (author)

  15. Study of Ni50+xMn25Ga25-x (x = 2-11) as high-temperature shape-memory alloys

    International Nuclear Information System (INIS)

    Ma Yunqing; Jiang Chengbao; Li Yan; Xu Huibin; Wang Cuiping; Liu Xingjun

    2007-01-01

    Ni 50+x Mn 25 Ga 25-x (x = 2-11) alloys were studied as high-temperature shape-memory alloys, with regard to their microstructure, martensitic transformation behavior and high-temperature shape-memory effect. Single phase of martensite with tetragonal structure was present for x p increase monotonically from 39.1 deg. C for x = 2 to 443.8 deg. C for x = 7, then remain almost constant at 440 deg. C for x ≥ 7. The shape-memory strains of the alloys decreased gradually from 6.1% for x = 4 to 2.8% for x = 8 and 0% for x = 11 under the same pre-strain. The variations of the martensitic transformation temperatures and the shape-memory effects with Ni contents correlate with changes in size factor, electron concentration and precipitation of γ phase

  16. Concentration and purification of plutonium solutions by means of ion-exchange columns

    Energy Technology Data Exchange (ETDEWEB)

    Durham, R W; Aikin, A M

    1953-02-15

    Equilibrium experiments using Dowex 50 ion-exchange resin and nitric acid solutions of Pu{sup 3+}, UO{sub 2}{sup 2+}, Fe{sup 2+} cations have yielded values for the absorption affinities for these ions. Trivalent plutonium was found to be far more strongly absorbed than UO{sub 2}{sup 2+} and Fe{sup 2+}. Column studies have shown that uranium can be completely separated from plutonium even when the initial concentration of uranium is very much greater than that of the plutonium. A plutonium concentration increase of about fifty-fold can be obtained from solutions about 10{sup -3} M in plutonium and 1.0M in nitric acid. The equation K{sub Pu}{sup 3+} = X{sub R} (1-X{sub S}){sup 3} C{sub S}{sup 2}/X{sub S} (1-X{sub R}){sup 3} C{sub R}{sup 2} for estimating the maximum amount of plutonium taken up by a column of resin of unit volume from a solution of total equivalent concentration, C{sub S} , has been shown to hold for values of C{sub S} up to 3 equivalents per litre. X{sub R}, the equivalent fraction of plutonium on the resin, is the number of equivalents of plutonium absorbed by the resin divided by the total capacity of the column. X{sub S}, the equivalent fraction of plutonium in solution, is the equivalent concentration of plutonium divided by the total equivalent concentration of cations in solution. C{sub R} is the total capacity of the resin in milli-equivalents per gram of dry resin. Recommendations have been made for the application and operation of ion-exchange columns in the Plutonium-Extraction Plant. (author)

  17. Additional chemical polymerization of dual resin cements: reality or a goal to be achieved?

    Directory of Open Access Journals (Sweden)

    Luzia Sakaguti UMETSUBO

    Full Text Available Abstract Introduction This study serves as a warning to dentists and researchers that dual-cured resin cements may not polymerize completely under some prosthetic crowns. Objective The aim of this study was to analyse the polymerization degree of dual-cured resin cements under prosthetic barrier, by microhardness test. Material and method Three cements (Bistite II, RelyX ARC and Variolink II were light-cured through different barriers, placed between the cement and the light source: G1: without barrier; G2: composite resin (Cesead; G3: Inceram alumina; G4: IPS Empress; G5: Inceram zirconia; G6: tooth fragment. Photopolymerization was carried out using a halogen light unit (650 mW/cm2; microhardness was evaluated using the Microhardness Tester FM 700, under a load of 50gf with a dwell time of 15s, at two evaluation times (30min and 24h. Result The results were submitted to ANOVA and Tukey tests (5%. Both Inceram alumina and Inceram zirconia ceramic barriers hindered polymerization. Bistite, followed by RelyX and Variolink, exhibited the highest microhardness values (p<0.05. As the highest values were obtained without a barrier, it was determined that the barrier, followed by the tooth, influenced microhardness. Both Empress and Cesead had the smallest microhardness values but with no statistically significant difference between them. Conclusion The barrier negatively affected the microhardness of dual-cured resin cements; evaluation time did not affect microhardness values for most of the conditions tested. There is a limited effect of the chemical activator on the polymerization of some dual-cured cements, and their performance is product specific.

  18. The asymptotic 3-loop heavy flavor corrections to the charged current structure functions F{sup W{sup +-W{sup -}{sub L}}}(x,Q{sup 2}) and F{sup W{sup +-W{sup -}{sub 2}}}(x,Q{sup 2})

    Energy Technology Data Exchange (ETDEWEB)

    Behring, A.; Bluemlein, J.; Falcioni, G.; Freitas, A. de [Deutsches Elektronen-Synchrotron (DESY), Zeuthen (Germany); Manteuffel, A. von [Michigan State Univ., East Lansing, MI (United States). Dept. of Physics and Astronomy; Mainz Univ. (Germany). PRISMA Cluster of Excellence; Schneider, C. [Johannes Kepler Univ., Linz (Austria). Research Inst. for Symbolic Computation

    2016-09-15

    We calculate the massive Wilson coefficients for the heavy flavor contributions to the non-singlet charged current deep-inelastic scattering structure functions F{sup W{sup +}{sub L}}(x,Q{sup 2})-F{sup W{sup -}{sub L}}(x,Q{sup 2}) and F{sup W{sup +}{sub 2}}(x,Q{sup 2}) - F{sup W{sup -}{sub 2}}(x,Q{sup 2}) in the asymptotic region Q{sup 2}>>m{sup 2} to 3-loop order in Quantum Chromodynamics (QCD) at general values of the Mellin variable N and the momentum fraction x. Besides the heavy quark pair production, also the single heavy flavor excitation s→c contributes. Numerical results are presented for the charm quark contributions and consequences on the unpolarized Bjorken sum rule and Adler sum rule are discussed.

  19. Preparation of carrier-free Phosphorus-32 from 31P(n,γ )32P reaction

    International Nuclear Information System (INIS)

    Rafii, H.; Arbab Zavar, H.; Avaz Moghadam, S.

    1999-01-01

    The phosphorus-32 is a widely used radioisotope as as tracer or radioactive source in nuclear medicine, and in many other biotechnical applications. In this paper, preparation of carrier-free P-32 with a high specific activity was studied by 31 P(n, γ) 32 P reaction. The anhydrous KH 2 PO 4 , as a target material, was irradiated in Tehran Nuclear Research Reactor with a neutron flux of 2.5x10 13 n/cm 2 .sec. The P-32 produced as a result of Szilard-Chalmers effect was isolated from the target by a strong anion exchange resin, (Dowex - X 8). The quality control of the product shows a high chemical, and radiochemical purity (>98%) and the increase specific activity depends on the irradiation time

  20. Effect of fiber inserts on gingival margin microleakage of Class II bulk-fill composite resin restorations.

    Science.gov (United States)

    Shafiei, Fereshteh; Doozandeh, Maryam; Karimi, Vahid

    2018-01-01

    This study evaluated the effect of fiber inserts combined with composite resins on enamel and dentin margin microleakage. The fiber inserts were used with high- (x-tra fil) and low-viscosity (x-tra base) bulk-fill composite resins and as well as conventional composite resins (Grandio and Grandio Flow). In 96 sound, recently extracted molars, 2 standardized Class II cavities were prepared. The teeth were randomly divided into 8 groups of 12 teeth each, based on composite resin type and presence or absence of fiber inserts: groups 1 and 2, x-tra fil with and without fiber inserts, respectively; groups 3 and 4, x-tra base with and without fiber inserts; groups 5 and 6, Grandio with and without fiber inserts; and groups 7 and 8, Grandio Flow liner (gingival floor)/Grandio (remainder of cavity) with and without fiber inserts. In all the groups, a 2-step etch-and-rinse adhesive was used. The specimens were processed in a dye penetration technique to determine microleakage percentages. Data were analyzed with analysis of variance, Tukey, and t tests. There was significantly less leakage at the enamel margins than the dentin margins. Fiber reinforcement significantly decreased enamel microleakage in all the groups, with no significant differences among the groups. Concerning dentin microleakage, there were no significant differences among the 4 groups without fiber inserts, while a significant difference was detected in groups 2 (x-tra fil plus fiber) and 8 (Grandio Flow plus fiber/Grandio). Fibers significantly improved dentin sealing in groups 2 and 8. These findings suggest that a fiber insert reinforcing bulk-fill and conventional composite resins might improve enamel sealing in shallow Class II cavi-ties. The effect of fiber reinforcement on the dentin margins of deep cavities depended on the viscosity of the composite resins; fiber reinforcement was effective for flowable bulk-fill and conventional composite resin restorations.

  1. Influence of composition on optical and dispersion parameters of thermally evaporated non-crystalline Cd{sub 50}S{sub 50x}Se{sub x} thin films

    Energy Technology Data Exchange (ETDEWEB)

    Hassanien, A.S., E-mail: a.s.hassanien@gmail.com [Engineering Mathematics and Physics Dept., Faculty of Engineering (Shoubra), Benha University (Egypt); Physics Department, Faculty of Science and Humanities in Ad-Dawadmi, Shaqra University, 11911 (Saudi Arabia); Akl, Alaa A. [Physics Department, Faculty of Science and Humanities in Ad-Dawadmi, Shaqra University, 11911 (Saudi Arabia)

    2015-11-05

    Non-crystalline thin films of chalcogenide Cd{sub 50}S{sub 50x}Se{sub x} system (30 ≤ x50) were obtained by thermal evaporation technique onto a pre-cleaned glass substrate at a vacuum of 8.2 × 10{sup −4} Pa. The deposition rate and film thickness were kept constant at about 8 nm/s and 200 nm, respectively. Amorphous/crystalline nature and chemical composition of films have been checked using X-ray diffraction and energy dispersive X-ray spectroscopy (EDX). Optical properties of thin films were investigated and studied using the corrected transmittance, T(λ) and corrected reflectance, R(λ) measurements. Obtained data reveal that, the indirect optical energy gap (E{sub g}) was decreased from 2.21 to 1.57 eV. On the contrary, Urbach energy (band tail width), E{sub U} was found to be increased from 0.29 to 0.45 eV. This behavior is believed to be associated with the increase of Se-content instead of S-content in the thin films of Cd{sub 50}S{sub 50x}Se{sub x} system. Chemical bond approach model, CBA was used to analyze the obtained values of E{sub g} and E{sub U}. Optical density, skin depth, extinction coefficient, refractive index and optical conductivity of chalcogenide CdSSe thin films were discussed as functions of Se-content. Using Wemple-DiDomenico single oscillator model, the refractive index dispersion and energy parameters and their dependence on Se content were studied. - Highlights: • Amorphous thin films of thickness 200 nm of Cd{sub 50}S{sub 50x}Se{sub x} (30 ≤ x50) have prepared. • Optical properties, indirect optical energy gap and band tail width were studied. • Chemical bond approach, CBA was used to analyze the obtained values of E{sub g} and E{sub U}. • New data of dispersion refractive index parameters were investigated and discussed.

  2. Development of method to chemical separation of gallium-67 by thermal diffusion technique

    International Nuclear Information System (INIS)

    Martins, Patricia de Andrade

    2012-01-01

    Radioisotopes of gallium have been studied and evaluated for medical applications since 1949. Over the past 50 years 67 Ga has been widely used in the diagnosis of various diseases, including acute and chronic inflammatory lesions, bacterial or sterile and several types of tumors. In Brazil 30% of clinics that provide services for Nuclear Medicine use 67 Ga citrate and the demand for 67 G a at IPEN-CNEN/SP is 37 GBq (1 Ci)/week. The 67 Ga presents physical half-life of 3.26 days (78 hours) and decays 100% by electron capture to stable 67 Zn. Its decay includes the emission of γ rays with energies of 93.3 keV (37%), 184.6 keV (20.4%), 300.2 keV (16.6%) and 888 keV (26%). In the past 67 Ga was produced by the reaction 68 Zn (p, 2n) 67 Ga at IPEN-CNEN/SP. After irradiation, the target was dissolved in concentrated HCl and the solution percolated through a cationic resin DOWEX 50W-X8, 200-400 mesh, conditioned with 10 mol L -1 HCl. Zinc, nickel and copper were eluted in 10 mol L -1 HCl and 67 Ga 3.5 mol L -1 HCl. The final product was obtained as 67 Ga citrate. This work presents a new, fast, direct and efficient method for the chemical separation of 67 G a by thermal diffusion (heating of the target) combined with concentrated acetic acid extraction. Purification was performed by ion exchange chromatography. Natural zinc electrodeposition was performed on nickel/copper plates as substrate and the zinc deposits were adherent to the substrate, slightly shiny and uniform. The targets were irradiated with 26 MeV protons and integrated current of 10 μA.h. After irradiation, the targets were heated at 300 deg C for 2 hours and placed in contact with concentrated acetic acid for 1 hour. The average yield of extraction of 67 Ga was (72 ± 10)%. This solution was evaporated and the residue was taken up in 0.5 mol L -1 NH 4 OH. The 67 G a was purified on cationic resin Dowex 50WX8 in NH 4 OH medium. The 67 Ga recovery was (98 ± 2)%. This solution was evaporated and taken up

  3. A study of adsorption equilibrium on quaternary ammonium resin in uranyl sulphate solution

    International Nuclear Information System (INIS)

    Xu Genfu; Xu Jiazhong; Zhu Jinghua

    1986-01-01

    Adsorption equilibrium on quaternary ammonium resin in uranyl sulphate solution, which is similar to composition used in uranium hydrometallurgy, was studied by chemical equivalent method. In the given range, the ratio of HSO 4 - to SO 4 2- on the resin is dependent on concentration of H + and ionic strength (μ) of solution, but it is independent of other anions sorbed on the resin. When the solution has μ of 0.1 to 0.5, pH of 1.5 to 1.9 and 0.5 x 10 -3 to 2.0 x 10 -3 M of uranium, the value of n in complex UO 2 (SO 4 ) n 2-2n is 2.5 to 2.7. The uranium occupies about 30% to 50% of total resin capacity

  4. Thermoanalytical Study and Kinetics of New 8-Hydroxyquinoline 5-sulphonic Acid-Oxamide-Formaldehyde Terpolymer Resins

    Directory of Open Access Journals (Sweden)

    Rajesh N. Singru

    2009-01-01

    Full Text Available The terpolymer resins (8-HQ5-SAOF have been synthesized by the condensation of 8-hydroxyquinoline 5-sulphonic acid (8-HQ5-SA and oxamide (O with formaldehyde (F in the presence of acid catalyst and using varied molar proportion of the reacting monomers. The synthesized terpolymer resins have been characterized by different physico-chemical techniques. Thermogravimetric analysis of all terpolymer resins in present study have been carried out by non-isothermal thermogravimetric analysis technique in which sample is subjected to condition of continuous increase in temperature at linear rate. Thermal study of the resins was carried out to determine their mode of decomposition and relative thermal stabilities. Thermal decomposition curves were studied carefully with minute details. The Freeman-Carroll and Sharp-Wentworth methods have been used in the present investigation to calculate thermal activation energy and different kinetic parameter of the terpolymer resins. Thermal activation energy (Ea calculated with above two mentioned methods are in close agreement. The advantage of Freeman-Carroll method is to calculate both the order of reaction (n and energy of activation in one single stage by keeping heating rate constant. By using data of thermogravimetric analysis, various thermodynamic parameters like frequency factor (Z, entropy change (Δ S, free energy change (Δ F and apparent entropy (S* have been determined using Freeman-Carroll method.

  5. Influences of W Content on the Phase Transformation Properties and the Associated Stress Change in Thin Film Substrate Combinations Studied by Fabrication and Characterization of Thin Film V1- xW xO2 Materials Libraries.

    Science.gov (United States)

    Wang, Xiao; Rogalla, Detlef; Ludwig, Alfred

    2018-04-09

    The mechanical stress change of VO 2 film substrate combinations during their reversible phase transformation makes them promising for applications in micro/nanoactuators. V 1- x W x O 2 thin film libraries were fabricated by reactive combinatorial cosputtering to investigate the effects of the addition of W on mechanical and other transformation properties. High-throughput characterization methods were used to systematically determine the composition spread, crystalline structure, surface topography, as well as the temperature-dependent phase transformation properties, that is, the hysteresis curves of the resistance and stress change. The study indicates that as x in V 1- x W x O 2 increases from 0.007 to 0.044 the crystalline structure gradually shifts from the VO 2 (M) phase to the VO 2 (R) phase. The transformation temperature decreases by 15 K/at. % and the resistance change is reduced to 1 order of magnitude, accompanied by a wider transition range and a narrower hysteresis with a minimal value of 1.8 K. A V 1- x W x O 2 library deposited on a Si 3 N 4 /SiO 2 -coated Si cantilever array wafer was used to study simultaneously the temperature-dependent stress change σ( T) of films with different W content through the phase transformation. Compared with σ( T) of ∼700 MPa of a VO 2 film, σ( T) in V 1- x W x O 2 films decreases to ∼250 MPa. Meanwhile, σ( T) becomes less abrupt and occurs over a wider temperature range with decreased transformation temperatures.

  6. Nature of low dimensional structural modulations and relative phase stability in RexMo(W)1-xS2 transition metal dichalcogenide alloys

    KAUST Repository

    Sahu, R.

    2017-03-08

    We report on the various types of Peierls like two dimensional structural modulations and relative phase stability of 2H and 1T poly-types in the RexMo1-xS2 and RexW1-xS2 alloy system. Theoretical calculation predicts a polytype phase transition cross over at ∼50 at. % of Mo and W in ReS2 in both monolayer and bulk form, respectively. Experimentally, two different types of structural modulations at 50% and a modulation corresponding to trimerization at 75% alloy composition are observed for RexMo1-xS2 and only one type of modulation is observed at the 50% RexW1-xS2 alloy system. The 50% alloy system is found to be a suitable monolithic candidate for metal semiconductor transition with minute external perturbation. ReS2 is known to be in the 2D Peierls distorted 1Td structure and forms a chain like superstructure. Incorporation of Mo and W atoms into the ReS2 lattice modifies the metal-metal hybridization between the cations and influences the structural modulation and electronic properties of the system. The results offer yet another effective way to tune the electronic structure and poly-type phases of this class of materials other than intercalation, strain, and vertical stacking arrangement.

  7. Removal of nitrate from ammonium hydroxide solution containing organics by ion exchange method

    International Nuclear Information System (INIS)

    Venugopal Chetty, K.; Gamare, Jayashree S.; Vaidya, V.N.

    2004-01-01

    Removal of nitrate from ammonium hydroxide solution containing HMTA (hexamethyltetramine) and Urea was studied using indigenously available anion exchange resins. This type of waste is produced during nuclear fuel preparation by internal gelation process. The resins used are Tulsion A-27(MP) and Duolite A. 102D. The time of equilibration and capacity of the resins were determined from distribution ratios obtained by equilibrating resin with nitrate solution. The loading, washing and elution behavior of nitrate on these resins were studied using synthetic mixture having similar composition of the waste produced. Elution studies were carried out using sodium hydroxide, hydrochloric acid and ammonium chloride. The studies were also carried out at higher temperature of around 60 degC. The data was compared with that obtained using Dowex 1x4 for the same purpose. (author)

  8. Plant start-up operation of treatment of liquid radioactive waste containing uranium in sulfuric acid by means of ion exchange

    International Nuclear Information System (INIS)

    Bustamante Escobedo, Mauricio

    2003-01-01

    The hydrometallurgy of uranium developed by CCHEN in the '80s generated different types of liquid radioactive waste: organic and aqueous, which have to be treated to extract the uranium, obtaining uranium concentrate less than 3 [ppm], in order to comply with the current regulations and to be able to be discharged as industrial waste over to specialized companies. The radioactive wastes were treated using strongly basic ion exchange resins to obtain a lower volume of concentrated uranium in solid phase. Batch processes were carried out with different pH values (1.4-1.6-1.7-1-8 and 2.0) and different residence times (5-10-15-240 [min]), to define the optimum processing conditions. Three resins were used: IONAC, AFP-329, IONAC A-641, DOWEX 11. The load capacities for each one were: 2[g/l], 1.85 [g/l] and 2.1 [g/l], respectively. Dowex 11 obtained the best uranium load results. Because of the nature of the treated solutions, the pH variation with sodium hydroxide generated precipitation and then crystallization of the existing pieces. Ninety-five percent of the resin's maximum load was attained after about 20 [min] of residence time. Continuous tests were carried out at the solution's original pH to verify the results obtained in the batch stage. This ion exchange process was compared with the chemical precipitation, with lime and sodium hydroxide as well as evaporation and in both processes the volumes of solid that were generated were significantly greater. The ion exchange plant worked with two serially connected columns, using 10 [l] of Dowex 11 resin in each one, with a residence time of 20 [min] per column. A total of 8 [m 3 ] of solution, obtaining an effluent with a uranium concentrate of less than 3 [ppm], using 140 [l] of resin, which generated an average load of 3 [g/l] of uranium (au)

  9. The Influence of Volume, Temperature and Flow Rate on the of Separation Ru from IRC-50 Amberlite Resin

    International Nuclear Information System (INIS)

    Murdani Sumarsono; Djoko Widodo

    2002-01-01

    It was studied Ru elution of IRC-50 amberlite resin for separating, Ru of resin bonding. The resin bonding was ion exchange result of spent fuel uranyl nitrate. In this experiment, the eluent was used 6 N HNO 3 solution the adsorption of Ru was 20 ppm and then it was eluted with 6 N HNO 3 eluent. The objective of this experiment was to determine the operation condition of elution proses that was based on the value of Ru release from its bonding as much as possible. Based on the experiment, the relative good condition were resin volume = 205 ml, elution temperature = 85 o C and the flow rate of eluent = 2 ml 6 N HNO 3 / minute and Ru as result was 93 %. (author)

  10. Sulfur geochemistry of hydrothermal waters in Yellowstone National Park, Wyoming, USA. III. An anion-exchange resin technique for sampling and preservation of sulfoxyanions in natural waters

    Directory of Open Access Journals (Sweden)

    Ball James W

    2003-06-01

    Full Text Available A sampling protocol for the retention, extraction, and analysis of sulfoxyanions in hydrothermal waters has been developed in the laboratory and tested at Yellowstone National Park and Green Lake, NY. Initial laboratory testing of the anion-exchange resin Bio-Rad™ AG1-X8 indicated that the resin was well suited for the sampling, preservation, and extraction of sulfate and thiosulfate. Synthetic solutions containing sulfate and thiosulfate were passed through AG1-X8 resin columns and eluted with 1 and 3 M KCl, respectively. Recovery ranged from 89 to 100%. Comparison of results for water samples collected from five pools in Yellowstone National Park between on-site IC analysis (U.S. Geological Survey mobile lab and IC analysis of resin-stored sample at SUNY-Stony Brook indicates 96 to 100% agreement for three pools (Cinder, Cistern, and an unnamed pool near Cistern and 76 and 63% agreement for two pools (Sulfur Dust and Frying Pan. Attempts to extract polythionates from the AG1-X8 resin were made using HCl solutions, but were unsuccessful. Bio-Rad™ AG2-X8, an anion-exchange resin with weaker binding sites than the AG1-X8 resin, is better suited for polythionate extraction. Sulfate and thiosulfate extraction with this resin has been accomplished with KCl solutions of 0.1 and 0.5 M, respectively. Trithionate and tetrathionate can be extracted with 4 M KCl. Higher polythionates can be extracted with 9 M hydrochloric acid. Polythionate concentrations can then be determined directly using ion chromatographic methods, and laboratory results indicate recovery of up to 90% for synthetic polythionate solutions using AG2-X8 resin columns.

  11. Ball milling and annealing of Co-50 at% W Powders

    CSIR Research Space (South Africa)

    Bolokang, AS

    2013-04-01

    Full Text Available Broadening and height reduction of X-ray diffraction peaks were observed after cold-pressing of unmilled Co-W pow- der mixture. It seems the effect of cold pressing has slightly reduced the lattice parameter of W from 3.165 to 3.143 Å. Consequent...

  12. Light curing through glass ceramics: effect of curing mode on micromechanical properties of dual-curing resin cements.

    Science.gov (United States)

    Flury, Simon; Lussi, Adrian; Hickel, Reinhard; Ilie, Nicoleta

    2014-04-01

    The aim of this study was to investigate micromechanical properties of five dual-curing resin cements after different curing modes including light curing through glass ceramic materials. Vickers hardness (VH) and indentation modulus (Y HU) of Panavia F2.0, RelyX Unicem 2 Automix, SpeedCEM, BisCem, and BeautiCem SA were measured after 1 week of storage (37 °C, 100 % humidity). The resin cements were tested following self-curing or light curing with the second-generation light-emitting diode (LED) curing unit Elipar FreeLight 2 in Standard Mode (1,545 mW/cm(2)) or with the third-generation LED curing unit VALO in High Power Mode (1,869 mW/cm(2)) or in XtraPower Mode (3,505 mW/cm(2)). Light curing was performed directly or through glass ceramic discs of 1.5 or 3 mm thickness of IPS Empress CAD or IPS e.max CAD. VH and Y HU were analysed with Kruskal-Wallis tests followed by pairwise Wilcoxon rank sum tests (α = 0.05). RelyX Unicem 2 Automix resulted in the highest VH and Y HU followed by BeautiCem SA, BisCem, SpeedCEM, and finally Panavia F2.0. Self-curing of RelyX Unicem 2 Automix and SpeedCEM lowered VH and Y HU compared to light curing whereas self-curing of Panavia F2.0, BisCem, and BeautiCem SA led to similar or significantly higher VH and Y HU compared to light curing. Generally, direct light curing resulted in similar or lower VH and Y HU compared to light curing through 1.5-mm-thick ceramic discs. Light curing through 3-mm-thick discs of IPS e.max CAD generally reduced VH and Y HU for all resin cements except SpeedCEM, which was the least affected by light curing through ceramic discs. The resin cements responded heterogeneously to changes in curing mode. The applied irradiances and light curing times adequately cured the resin cements even through 1.5-mm-thick ceramic discs. When light curing resin cements through thick glass ceramic restorations, clinicians should consider to prolong the light curing times even with LED curing units providing high

  13. Design and manufacturing concrete cells for shielding and storing radioactive semi liquid waste (resin) from MPR-GAS

    International Nuclear Information System (INIS)

    Pudjijanto-MS; Bahdir-Johan

    2003-01-01

    Semi liquid or quasi solid waste on Multipurpose Reactor G.A. Siwabessy (MPR-GAS) produced from operating resin rinsing systems and resin disposal systems during changes insert trap resin. Volume of the disposal resin waste in the filter mixed-bed per operation rinsing period are approx. 1.00 m 3 (in the Primary Cooling Water Treatment System) with activity ∼ 18.6 Ci/m 3 (0.688 TBq/m 3 ), 0.50 m 3 (in the Radioisotope Storage Pool Water Treatment System) with activity approx ∼ 0.162 Ci/m 3 (5.99 x 10 3 MBq/m 3 ) and 0.50 m 3 (in the Interim Spent Fuel Storage Pool Water Treatment System) with activity ∼ 0.162 Ci/m 3 (5.99 x 10 3 MBq/m 3 ) respectively. On the discharging and unloading, the gross radioactivity concentration of the resin waste loaded in the disposal resin waste tank are approx. 10 Ci/m 3 (0.37 TBq/m 3 ). After 6 months delayed, this activity is still 0.32 Ci/m 3 (11.84 GBq/m 3 ). Based on this data, some concrete cells to storage resin waste as semi liquid or quasi solid waste produced continuously by MPR-GAS installation has been designed and manufactured eternally

  14. Sulfur geochemistry of hydrothermal waters in Yellowstone National Park, Wyoming, USA. III. An anion-exchange resin technique for sampling and preservation of sulfoxyanions in natural waters

    Science.gov (United States)

    Druschel, G.K.; Schoonen, M.A.A.; Nordstorm, D.K.; Ball, J.W.; Xu, Y.; Cohn, C.A.

    2003-01-01

    A sampling protocol for the retention, extraction, and analysis of sulfoxyanions in hydrothermal waters has been developed in the laboratory and tested at Yellowstone National Park and Green Lake, NY. Initial laboratory testing of the anion-exchange resin Bio-Rad??? AG1-X8 indicated that the resin was well suited for the sampling, preservation, and extraction of sulfate and thiosulfate. Synthetic solutions containing sulfate and thiosulfate were passed through AG1-X8 resin columns and eluted with 1 and 3 M KCl, respectively. Recovery ranged from 89 to 100%. Comparison of results for water samples collected from five pools in Yellowstone National Park between on-site IC analysis (U.S. Geological Survey mobile lab) and IC analysis of resin-stored sample at SUNY-Stony Brook indicates 96 to 100% agreement for three pools (Cinder, Cistern, and an unnamed pool near Cistern) and 76 and 63% agreement for two pools (Sulfur Dust and Frying Pan). Attempts to extract polythionates from the AG1-X8 resin were made using HCl solutions, but were unsuccessful. Bio-Rad??? AG2-X8, an anion-exchange resin with weaker binding sites than the AG1-X8 resin, is better suited for polythionate extraction. Sulfate and thiosulfate extraction with this resin has been accomplished with KCl solutions of 0.1 and 0.5 M, respectively. Trithionate and tetrathionate can be extracted with 4 M KCl. Higher polythionates can be extracted with 9 M hydrochloric acid. Polythionate concentrations can then be determined directly using ion chromatographic methods, and laboratory results indicate recovery of up to 90% for synthetic polythionate solutions using AG2-X8 resin columns. ?? The Royal Society of Chemistry and the Division of Geochemistry of the American Chemical Society 2003.

  15. Conceptual design of pellet charge eXchange (PCX) diagnostics for stellarator W7-X

    International Nuclear Information System (INIS)

    Sergeev, Y.Yu; Kuteev, B.V.; Bakhareva, O.A.; Kostrukov, A.Y.; Skokov, V.G.; Petrov, M.P.; Kislyakov, A.I.; Burhenn, R.; Kick, M.

    2002-01-01

    Pellet Charge eXchange diagnostic using Li pellets has been considered for the W7-X machine. Geometry of the experimental set-up and parameters of both lithium pellet injector (LPI) and neutral particle analyser (NPA) were evaluated. It was shown that this diagnostics can provide very well detectable H 0 signal in the range 50 - 1000 keV generated by RF driven H + minority ions in W7-X. The PCX diagnostics will be able to measure H + energy spectra and density profiles in wide range of W7-X plasma parameters. The proposed NPA can be designed on a basis of the NPA ISEP (Ioffe institute) installed now on JET. A pellet light-gas gun can be used to accelerate Li pellets of 2 - 3 mm in size up to 1 km/s velocities. That provides the required pellet penetration into the plasma core. Due to sticky problems with Li operation, a special technique of loading and keeping the pellets in a charger unit of LPI has to be developed. Development of PCX diagnostics for absolute measurements of the confined minority protons requires improvement of the pellet ablation model used. Knowledge of the cloud dimensions and density distributions of different charge states of ions is of special interest. It is necessary to improve predictions of pellet penetrations in non-Maxwellian plasmas as well. An optical system for measurements of pellet cloud density profiles should be foreseen on W7-X. (orig.)

  16. Extraction of the width of the $W$ boson from a measurement of the ratio of the $W$ and $Z$ cross-sections

    Energy Technology Data Exchange (ETDEWEB)

    Gomez, Gervasio [Univ. of Maryland, College Park, MD (United States)

    1999-01-01

    This dissertation reports on measurements of inclusive cross sections times branching fractions into electrons for W and Z bosons produced in pp collisions at ps = 1.8 TeV. From an integrated luminosity of 84.5 pb-1 recorded in 1994-1995 by the D0 detector at the Fermilab Tevatron, the cross sections are measured to be (p$\\bar{p}$ → W +X) ∙ B(W → e )= 2310 ± 10 (stat) ± 50 (syst) ± 100 (lum) pb and (p$\\bar{p}$ → Z +X) ∙ B(Z → ee)= 221 ± 3 (stat) ± 4 (syst) ± 10 (lum) pb. The cross section ratio R is determined to be (p$\\bar{p}$ → W+X) B(W → e )= (p$\\bar{p}$ → Z + X) ∙ B(Z → ee) = 10.43 ± 0.15 (stat) 0.20 (syst) ± 0.10 (NLO), and R is used to determine B(W → ev ) = 0.1044 ± 0.0015 (stat) ± 0.0020 (syst) 0.0017 (theory) ± 0.0010 (NLO), and W = 2.169 ± 0.031 (stat) ± 0.042 (syst) 0.041 (theory) ± 0.022 (NLO) GeV. The latter is used to set a 95% confidence level upper limit on the partial decay width of the W boson into non-standard model final states, $inv\\atop{W}$ , of 0.213 GeV.

  17. Analysis of long-term monomer elution from bulk-fill and conventional resin-composites using high performance liquid chromatography.

    Science.gov (United States)

    Alshali, Ruwaida Z; Salim, Nesreen A; Sung, Rehana; Satterthwaite, Julian D; Silikas, Nick

    2015-12-01

    The aim of this study was to assess monomer elution from bulk-fill and conventional resin-composites stored in different media using high performance liquid chromatography (HPLC) for up to 3 months. Six bulk-fill (SureFil SDR, Venus Bulk Fill, X-tra base, Filtek Bulk Fill flowable, Sonic Fill, and Tetric EvoCeram Bulk Fill) and eight conventional resin-composites (Grandioso Flow, Venus Diamond Flow, X-Flow, Filtek Supreme XTE, Grandioso, Venus Diamond, TPH Spectrum, and Filtek Z250) were tested. Cylindrical samples (n=5) were immersed in water, 70% ethanol/water solution (70% E/W), and artificial saliva and stored at 37°C for 24h, 1 month, and 3 months. The storage solutions were analysed with HPLC. Data were analysed with repeated measures ANOVA, one-way ANOVA, and Tukey post hoc test at α=0.05. Monomers detected in water and artificial saliva were TEGDMA, DEGDMA, UDMA, and TCD-DI-HEA. No eluted monomers were detected from X-tra base and Sonic fill in these media. All monomers showed a variable extent of elution into 70% E/W with significantly higher amounts than those detected in water and artificial saliva. Significantly higher elution was detected from UDMA-BisEMA based composites compared to BisGMA and BisGMA-BisEMA based systems in 70% E/W. The rate of elution into different media varied between different monomers and was highly dependent on the molecular weight of the eluted compounds. Elution from bulk-fill resin-composites is comparable to that of conventional materials despite their increased increment thickness. Monomer elution is highly dependent on the hydrophobicity of the base monomers and the final network characteristics of the resin-matrix. Copyright © 2015 Academy of Dental Materials. Published by Elsevier Ltd. All rights reserved.

  18. Separation of 99Mo from 132Te using thiourea as complexing agent. Application to the separation of 99Mo from the fission products

    International Nuclear Information System (INIS)

    Mestnik, S.A.C.

    1987-01-01

    A radiochemical method to isolate 99 Mo from 132 Te both produced in the fission of 235 U has been developed. The method is based on the formation of a cationic complex of tellurium with thiourea in acid medium wich is retained (98.7+-0.5) % on a cation exchange resin (Dowex 50W-X8, 100-200 mesh) wile (99.8+-0.05)% 99 Mo passes through it, due to the non formation of such complex in the same experimental conditions. The radiochemical purity of the separated 99 Mo verified by using gamma spectrometry was found to be suitable for the preparation of 99 Mo- 99m Tc generators. The retention of 99 Mo on an alumina column as function of pH was investigated. The best pH range for this purpose was found to be between 4.0-4.5. Yellow crystals with melting point of 115 0 C were formed when non-irradiated tellurium reacted with thiourea. Elemental analysis, ultra-violet and infra-red absorption spectrophotometry as well as thermogravimetry were used to characterize the complex formed. In the studies made in order to characterize the compound it has been observed: 1. the most probable chemical composition of the complex studied is [Te(SCN 2 H 4 ) 4 ] (SO 4 ) 2 ; 2. the coordination takes place between tellurium and sulphur atoms; 3. the maximum absorption in the ultra-violet region occurs near 310nm. The thermogravimetric curves obtained allowed to propose the concerned thermodecomposition mechanism. (author) [pt

  19. Fracture Resistance of Lithium Disilicate Ceramics Bonded to Enamel or Dentin Using Different Resin Cement Types and Film Thicknesses.

    Science.gov (United States)

    Rojpaibool, Thitithorn; Leevailoj, Chalermpol

    2017-02-01

    To investigate the influence of cement film thickness, cement type, and substrate (enamel or dentin) on ceramic fracture resistance. One hundred extracted human third molars were polished to obtain 50 enamel and 50 dentin specimens. The specimens were cemented to 1-mm-thick lithium disilicate ceramic plates with different cement film thicknesses (100 and 300 μm) using metal strips as spacers. The cements used were etch-and-rinse (RelyX Ultimate) and self-adhesive (RelyX U200) resin cements. Compressive load was applied on the ceramic plates using a universal testing machine, and fracture loads were recorded in Newtons (N). Statistical analysis was performed by multiple regression (p enamel showed the highest mean fracture load (MFL; 1591 ± 172.59 N). The RelyX Ultimate groups MFLs were significantly higher than the corresponding RelyX U200 groups (p enamel (p enamel. Reduced resin film thickness could reduce lithium disilicate restoration fracture. Etch-and-rinse resin cements are recommended for cementing on either enamel or dentin, compared with self-adhesive resin cement, for improved fracture resistance. © 2015 by the American College of Prosthodontists.

  20. Evaluation of temperature rise with different curing methods and units in two composite resins

    Directory of Open Access Journals (Sweden)

    Tabatabaei M

    2006-01-01

    Full Text Available Background and Aim: The majority of commercial curing units in dentistry are of halogen lamp type. The new polymerizing units such as blue LED are introduced in recent years. One of the important side effects of light curing is the temperature rise in composite resin polymerization which can affect the vitality of tooth pulp. The purpose of this study was to evaluate the temperature rise in two different composite resins during polymerization with halogen lamps and blue LED. Materials and Methods: This experimental study investigated the temperature rise in two different composites (Hybrid, Tetric Ceram/Nanofilled, Filteke Supreme of A2 shade polymerized with two halogen lamps (Coltolux 50, 350 mW/cm2 and Optilux 501 in standard, 820 mW/cm2 and Ramp, 100-1030 mW/cm2 operating modes and one blue LED with the intensity of 620 mW/cm2. Five samples for each group were prepared and temperature rise was monitored using a k-type thermocouple. Data were analyzed by one-way ANOVA, two-way ANOVA and Tukey HSD tests with P<0.05 as the limit of significance. Results: Light curing units and composite resins had statistically significant influence on the temperature rise (p<0.05. Significantly, lower temperature rise occurred in case of illumination with Coltolux 50.There was no significant difference between Optilux 501 in standard curing mode and LED. Tetric Ceram showed higher temperature rise. Conclusion: According to the results of this study the high power halogen lamp and LED could produce significant heat which may be harmful to the dental pulp.

  1. Magnetic spin configuration in Fe{sub 50}Pt{sub 50-x}Rh{sub x} alloys

    Energy Technology Data Exchange (ETDEWEB)

    Fenske, J.; Lott, D.; Schreyer, A. [GKSS Research Centre (Germany); Mankey, G.J. [University of Alabama, MINT Center (United States); Schmidt, W.; Schmalzl, K. [Juelich Research Centre (Germany); Tartakowskaya, E. [Institute for Magnetism, National Ukrainian Accademy of Science (Ukraine)

    2010-07-01

    FePt-based alloys are typically the material of choice for magnetic information storage media. The high magnetic moment of Fe gives a large magnetization and the large atomic number of Pt results in a high magnetic anisotropy. This combination enables the written bits to be smaller than ever before. One way to control the magnetic properties in these materials is through the introduction of a third element into the crystal matrix e.g. Rh. When Rh is added to replace Pt in the equiatomic alloy, new magnetic phases emerge. Bulk samples of Fe{sub 50}Pt{sub 50-x}Rh{sub x} studied by magnetization measurements refer to three different phase transitions with increasing temperature: (I) An antiferromagnetic (AF)-paramagnetic (PM) transition for 30<x<14.25, (II), an AF-ferromagnetic (FM) transition for 14.25<x<9.5 and, (III), a FM-PM transition 9.5<x<0. Here we present results on a series of 200 nm Fe{sub 50}Pt{sub 50-x}Rh{sub x} films with different Rh concentrations. These films were examined by neutron diffraction in dependence of temperature and magnetic field. By the use of polarized and unpolarized neutron diffraction we could develop a detailed model of the magnetic spin structure in these thin films.

  2. Enhanced vanillin production from ferulic acid using adsorbent resin.

    Science.gov (United States)

    Hua, Dongliang; Ma, Cuiqing; Song, Lifu; Lin, Shan; Zhang, Zhaobin; Deng, Zixin; Xu, Ping

    2007-03-01

    High vanillin productivity was achieved in the batch biotransformation of ferulic acid by Streptomyces sp. strain V-1. Due to the toxicity of vanillin and the product inhibition, fed-batch biotransformation with high concentration of ferulic acid was unsuccessful. To solve this problem and improve the vanillin yield, a biotransformation strategy using adsorbent resin was investigated. Several macroporous adsorbent resins were chosen to adsorb vanillin in situ during the bioconversion. Resin DM11 was found to be the best, which adsorbed the most vanillin and the least ferulic acid. When 8% resin DM11 (wet w/v) was added to the biotransformation system, 45 g l(-1) ferulic acid could be added continually and 19.2 g l(-1) vanillin was obtained within 55 h, which was the highest vanillin yield by bioconversion until now. This yield was remarkable for exceeding the crystallization concentration of vanillin and therefore had far-reaching consequence in its downstream processing.

  3. Mercury(II) and methyl mercury speciation on Streptococcus pyogenes loaded Dowex Optipore SD-2

    International Nuclear Information System (INIS)

    Tuzen, Mustafa; Uluozlu, Ozgur Dogan; Karaman, Isa; Soylak, Mustafa

    2009-01-01

    A solid phase extraction procedure based on speciation of mercury(II) and methyl mercury on Streptococcus pyogenes immobilized on Dowex Optipore SD-2 has been established. Selective and sequential elution with 0.1 mol L -1 HCl for methyl mercury and 2 mol L -1 HCl for mercury(II) were performed at pH 8. The determination of mercury levels was performed by cold vapour atomic absorption spectrometry (CVAAS). Optimal analytical conditions including pH, amounts of biosorbent, sample volumes, etc., were investigated. The influences of the some alkaline and earth alkaline ions and some transition metals on the recoveries were also investigated. The capacity of biosorbent for mercury(II) and methyl mercury was 4.8 and 3.4 mg g -1 . The detection limit (3 sigma) of the reagent blank for mercury(II) and methyl mercury was 2.1 and 1.5 ng L -1 . Preconcentration factor was calculated as 25. The relative standard deviations of the procedure were below 7%. The validation of the presented procedure is performed by the analysis of standard reference material (NRCC-DORM 2 Dogfish Muscle). The procedure was successfully applied to the speciation of mercury(II) and methyl mercury in natural water and environmental samples.

  4. Mercury(II) and methyl mercury speciation on Streptococcus pyogenes loaded Dowex Optipore SD-2

    Energy Technology Data Exchange (ETDEWEB)

    Tuzen, Mustafa, E-mail: m.tuzen@gmail.com [Gaziosmanpasa University, Faculty of Science and Arts, Chemistry Department, 60250 Tokat (Turkey); Uluozlu, Ozgur Dogan [Gaziosmanpasa University, Faculty of Science and Arts, Chemistry Department, 60250 Tokat (Turkey); Karaman, Isa [Gaziosmanpasa University, Faculty of Science and Arts, Biology Department, 60250 Tokat (Turkey); Soylak, Mustafa [Erciyes University, Faculty of Science and Arts, Chemistry Department, 38039 Kayseri (Turkey)

    2009-09-30

    A solid phase extraction procedure based on speciation of mercury(II) and methyl mercury on Streptococcus pyogenes immobilized on Dowex Optipore SD-2 has been established. Selective and sequential elution with 0.1 mol L{sup -1} HCl for methyl mercury and 2 mol L{sup -1} HCl for mercury(II) were performed at pH 8. The determination of mercury levels was performed by cold vapour atomic absorption spectrometry (CVAAS). Optimal analytical conditions including pH, amounts of biosorbent, sample volumes, etc., were investigated. The influences of the some alkaline and earth alkaline ions and some transition metals on the recoveries were also investigated. The capacity of biosorbent for mercury(II) and methyl mercury was 4.8 and 3.4 mg g{sup -1}. The detection limit (3 sigma) of the reagent blank for mercury(II) and methyl mercury was 2.1 and 1.5 ng L{sup -1}. Preconcentration factor was calculated as 25. The relative standard deviations of the procedure were below 7%. The validation of the presented procedure is performed by the analysis of standard reference material (NRCC-DORM 2 Dogfish Muscle). The procedure was successfully applied to the speciation of mercury(II) and methyl mercury in natural water and environmental samples.

  5. Speciation of arsenic in water samples by high-performance liquid chromatography-hydride generation-atomic absorption spectrometry at trace levels using a post-column reaction system

    Energy Technology Data Exchange (ETDEWEB)

    Stummeyer, J. [Bundesanstalt fuer Geowissenschaften und Rohstoffe, Hannover (Germany); Harazim, B. [Bundesanstalt fuer Geowissenschaften und Rohstoffe, Hannover (Germany); Wippermann, T. [Bundesanstalt fuer Geowissenschaften und Rohstoffe, Hannover (Germany)

    1996-02-01

    Anion-exchange HPLC has been combined with hydride generation - atomic absorption spectrometry (HG-AAS) for the routine speciation of arsenite, arsenate, monomethylarsenic acid and dimethylarsinic acid. The sensitivity of the AAS-detection was increased by a post-column reaction system to achieve complete formation of volatile arsines from the methylated species and arsenate. The system allows the quantitative determination of 0.5 {mu}g/l of each arsenic compound in water samples. The stability of synthetical and natural water containing arsenic at trace levels was investigated. To preserve stored water samples, a method for quantitative separation of arsenate at high pH-values with the basic anion-exchange resin Dowex 1 x 8 was developed. (orig.)

  6. A computational study on the energetics and mechanisms for the dissociative adsorption of SiH{sub x}(x = 1–4) on W(1 1 1) surface

    Energy Technology Data Exchange (ETDEWEB)

    Lin, Y.H.; Raghunath, P.; Lin, M.C., E-mail: chemmcl@emory.edu

    2016-01-30

    Graphical abstract: - Highlights: • Behavior of the SiH{sub x} species on the W surface under cat-CVD conditions. • The adsorption and dissociation mechanisms of SiH{sub x}(x = 1–4) species on W(1 1 1) surface. • H-migration to its neighboring W atoms is more favorable compared to H{sub 2} elimination. - Abstract: The adsorption and dissociation mechanisms of SiH{sub x}(x = 1–4) species on W(1 1 1) surface have been investigated by using the periodic density functional theory with the projector-augmented wave approach. The adsorption of all the species on four surface sites: top (T), bridge (B), shallow (S), and deep (D) sites have been analyzed. For SiH{sub 4} on a top site, T-SiH{sub 4(a)}, it is more stable with an adsorption energy of 2.6 kcal/mol. For SiH{sub 3}, the 3-fold shallow site is most favorable with adsorption energy of 46.0 kcal/mol. For SiH{sub 2}, its adsorption on a bridge site is most stable with 73.0 kcal/mol binding energy, whereas for SiH and Si the most stable adsorption configurations are on 3-fold deep sites with very high adsorption energies, 111.8 and 134.7 kcal/mol, respectively. The potential energy surfaces for the dissociative adsorption of all SiH{sub x} species on the W(1 1 1) surface have been constructed using the CINEB method. The barriers for H-atom migration from SiH{sub x(a)} to its neighboring W atoms, preferentially on B-sites, were predicted to be 0.4, 1.0, 4.5 and, 8.0 kcal/mol, respectively, for x = 4, 3, 2, and 1, respectively. The adsorption energy of the H atom on a bridge site on the clean W(1 1 1) surface was predicted to be 65.9 kcal/mol, which was found to be slightly affected by the co-adsorption of SiH{sub x−1} within ± 1 kcal/mol.

  7. Mercuric iodide semiconductor detectors encapsulated in polymeric resin

    Energy Technology Data Exchange (ETDEWEB)

    Martins, Joao F. Trencher; Santos, Robinson A. dos; Ferraz, Caue de M.; Oliveira, Adriano S.; Velo, Alexandre F.; Mesquita, Carlos H. de; Hamada, Margarida M., E-mail: mmhamada@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil); Disch, Christian; Fiederle, Michael [Albert-Ludwigs Universität Freiburg - UniFreibrug, Freiburg Materials Research Center - FMF, Freiburg (Germany)

    2015-07-01

    The development of new semiconductor radiation detectors always finds many setback factors, such as: high concentration of impurities in the start materials, poor long term stability, the surface oxidation and other difficulties discussed extensively in the literature, that limit their use. In this work was studied, the application of a coating resin on HgI2 detectors, in order to protect the semiconductor crystal reactions from atmospheric gases and to isolate electrically the surface of the crystals. Four polymeric resins were analyzed: Resin 1: 50% - 100%Heptane, 10% - 25% methylcyclohexane, <1% cyclohexane; Resin 2: 25% - 50% ethanol, 25% - 50% acetone, <2,5% ethylacetate; Resin 3: 50% - 100% methylacetate, 5% - 10% n-butylacetate; Resin 4: 50% - 100% ethyl-2-cyanacrylat. The influence of the polymeric resin type used on the spectroscopic performance of the HgI{sub 2} semiconductor detector is, clearly, demonstrated. The better result was found for the detector encapsulated with Resin 3. An increase of up to 26 times at the stability time was observed for the detectors encapsulated compared to that non-encapsulated detector. (author)

  8. Effect of light aging on silicone-resin bond strength in maxillofacial prostheses.

    Science.gov (United States)

    Polyzois, Gregory; Pantopoulos, Antonis; Papadopoulos, Triantafillos; Hatamleh, Muhanad

    2015-04-01

    The aim of this study was to investigate the effect of accelerated light aging on bond strength of a silicone elastomer to three types of denture resin. A total of 60 single lap joint specimens were fabricated with auto-, heat-, and photopolymerized (n = 20) resins. An addition-type silicone elastomer (Episil-E) was bonded to resins treated with the same primer (A330-G). Thirty specimens served as controls and were tested after 24 hours, and the remaining were aged under accelerated exposure to daylight for 546 hours (irradiance 765 W/m(2) ). Lap shear joint tests were performed to evaluate bond strength at 50 mm/min crosshead speed. Two-way ANOVA and Tukey's test were carried out to detect statistical significance (p Accelerated light aging for 546 hours affects the bond strength of an addition-type silicone elastomer to three different denture resins. The bond strength significantly increased after aging for photo- and autopolymerized resins. All the bonds failed adhesively. © 2014 by the American College of Prosthodontists.

  9. Separation of Actinium 227 from the uranium minerals

    International Nuclear Information System (INIS)

    Martinez-Tarango, S.

    1991-01-01

    The purpose of this work was to separate Actinium 227, whose content is 18%, from the mineral carnotite found in Gomez Chihuahua mountain range in Mexico. The mineral before processing is is pre-concentrated and passed, first through anionic exchange resins, later the eluate obtained is passed through cationic resins. The resins were 20-50 MESH QOWEX and 100-200 MESH 50 X 8-20 in some cased 200-400 MESH AG 50W-X8, 1X8 in other cases. The eluates from the ionic exchange were electrodeposited on stainless steel polished disc cathode and platinum electrode as anode; under a current ODF 10mA for 2.5 to 5 hours and of 100mA for .5 of an hour. it was possible to identify the Actinium 227 by means of its descendents, TH-227 and RA-223, through alpha spectroscopy. Due to the radiochemical purity which the electro deposits were obtained the Actinium 227 was low and was not quantitatively determined. A large majority of the members of the natural radioactive series 3 were identified and even alpha energies reported in the literature with very low percentages of non-identified emissions were observed. We conclude that a more precise study is needed concerning ionic exchange and electrodeposit to obtain an Actinium 227 of radiochemical purity. (Author)

  10. Application of neutron activation techniques and x-ray energy dispersion spectrometry, in analysis of metallic traces adsorbed by chelex-100 resin

    International Nuclear Information System (INIS)

    Fernandes, Jair C.; Amaral, Angela M.; Magalhaes, Jesus C.; Pereira, Jose S.J.; Silva, Juliana B. da; Auler, Lucia M.L.A.

    2000-01-01

    In this work, the authors have investigated optimal conditions of adsorption for several ion metallic groups (cations of heavy metals and transition metals, oxyanions metallics and metalloids and cations of rare earths), as traces (ppb), withdrawn and in mixture of groups, by chelex-100 resin. The experiments have been developed by bath techniques in ammonium acetate tamponade solution 40 mM pH 5,52 content 0,5 g of chelex-100 resin. After magnetic agitation for two hours, resins were dried and submitted to X-ray energy dispersion spectrometry, x-ray fluorescence spectrometry and neutron activation analysis. The results have demonstrated that chelex-100 resin adsorb quantitatively transition element groups and rare earth groups in two cases (withdrawn and simultaneously adsorption)

  11. Southwest Atlantic Ocean Marathon Expedition, Leg 8.

    Science.gov (United States)

    1986-07-01

    WEST 36.0OS 530 52* 51* 500 490 46* 470 460 450 440 43v 420 w X~ 400- w~ 600-~ 5 5 27-29 OCT 1984 35.50S LONGITUDE WEST 3%50 53’ 52’ 51’ 50* 490 48...b.8 K0$b.8 OKj/h.8 N../Kc JAC fta /s..2 N/S 10.41/5.4 1.0 1.0164111 16.416 36.711 26. 190 26 196 is.1 £611.6 016 10 1522.6 0 310 10.9 16.46 1641 28707...0.0 2.0 4.0 6.0 8.0 10.0 12.0 14.0 16.0 18.0 20.0 o 24.0 25.0 26.0 27.0 28.0 20- i8 16 A6 14 - /- hi 12 / . o 6 0 4 - 2 0 Nile -2 . 32.0 33.0 340 350

  12. Evaluation of internal adaptation of Class V resin composite restorations using three techniques of polymerization

    Directory of Open Access Journals (Sweden)

    José Carlos Pereira

    2007-02-01

    Full Text Available OBJECTIVE: The purpose of this in vitro study was to evaluate the internal adaptation of Class V composite restorations to the cavity walls using three different techniques of polymerization. METHODS: Standard cavities were prepared on the buccal and lingual surfaces of 24 extracted human third molars with margins located above and below the cementoenamel junction. Restorations were placed in one increment using two restorative systems: 3M Filtek A110/ Single Bond (M and 3M Filtek Z250/ Single Bond (H in the same tooth, randomly in the buccal and lingual surfaces. Resin composites were polymerized using three techniques: Group 1 - Conventional (60 s - 600 mW/cm²; Group 2 - Soft-start (20 s - 200 mW/cm² , 40 s - 600 mW/cm²; Group 3 - Pulse Activation (3 s - 200 mW/cm², 3-min hiatus, 57 s - 600 mW/cm². Buccolingual sections were polished, impressions taken and replicated. Specimens were assessed under scanning electron microscopy up to X1000 magnification. Scores were given for presence or absence of gaps (0 - no gap; 1 - gap in one wall; 2 - gap in two walls; 3 - gap in three walls. RESULTS: The mean scores of the groups were (±SD were: G1M-3.0 (± 0.0; G2M-2.43 (± 0.8; G3M- 1.71 (± 0.9; G1H- 2.14 (± 1.2; G2H- 2.00 (± 0.8; G3H- 1.67 (± 1.1. Data were analyzed using Kruskal-Wallis and Dunnet's tests. No statistically significant difference (p>0.05 was found among groups. Gaps were observed in all groups. CONCLUSIONS: The photocuring technique and the type of resin composite had no influence on the internal adaptation of the material to the cavity walls. A positive effect was observed when the slow polymerization techniques were used.

  13. Thermal expansion studies of ThW2O8 and UWO6

    International Nuclear Information System (INIS)

    Keskar, Meera; Krishnan, K.; Sali, S.K.

    2014-01-01

    Thorium and uranium oxysalts with hexavalent cations of elements of VI th group of the periodic table are important from mineralogical, environmental and technological points of view. Several molybdates and tungstates of uranium and thorium are known to have similar structural and thermo-physical properties. Earlier, thermal expansion behavior of ThMo 2 O 8 and UMoO 6 were reported from our laboratory. In the present work, thermal expansion behavior of ThW 2 O 8 and UWO 6 studied under vacuum from ambient to 1000 and 800℃, respectively using high temperature X-ray diffraction (HTXRD) technique is reported

  14. High performance dental resin composites with hydrolytically stable monomers.

    Science.gov (United States)

    Wang, Xiaohong; Huyang, George; Palagummi, Sri Vikram; Liu, Xiaohui; Skrtic, Drago; Beauchamp, Carlos; Bowen, Rafael; Sun, Jirun

    2018-02-01

    The objectives of this project were to: 1) develop strong and durable dental resin composites by employing new monomers that are hydrolytically stable, and 2) demonstrate that resin composites based on these monomers perform superiorly to the traditional bisphenol A glycidyl dimethacrylate/triethylene glycol dimethacrylate (Bis-GMA/TEGDMA) composites under testing conditions relevant to clinical applications. New resins comprising hydrolytically stable, ether-based monomer, i.e., triethylene glycol divinylbenzyl ether (TEG-DVBE), and urethane dimethacrylate (UDMA) were produced via composition-controlled photo-polymerization. Their composites contained 67.5wt% of micro and 7.5wt% of nano-sized filler. The performances of both copolymers and composites were evaluated by a battery of clinically-relevant assessments: degree of vinyl conversion (DC: FTIR and NIR spectroscopy); refractive index (n: optical microscopy); elastic modulus (E), flexural strength (F) and fracture toughness (K IC ) (universal mechanical testing); Knoop hardness (HK; indentation); water sorption (W sp ) and solubility (W su ) (gravimetry); polymerization shrinkage (S v ; mercury dilatometry) and polymerization stress (tensometer). The experimental UDMA/TEG-DVBE composites were compared with the Bis-GMA/TEGDMA composites containing the identical filler contents, and with the commercial micro hybrid flowable composite. UDMA/TEG-DBVE composites exhibited n, E, W sp , W su and S v equivalent to the controls. They outperformed the controls with respect to F (up to 26.8% increase), K IC (up to 27.7% increase), modulus recovery upon water sorption (full recovery vs. 91.9% recovery), and stress formation (up to 52.7% reduction). In addition, new composites showed up to 27.7% increase in attainable DC compared to the traditional composites. Bis-GMA/TEGDMA controls exceeded the experimental composites with respect to only one property, the composite hardness. Significantly, up to 18.1% lower HK values in

  15. Effects of He{sup +} ion implantation on surface properties of UV-cured Bis-GMA/TEGDMA bio-compatible resins

    Energy Technology Data Exchange (ETDEWEB)

    Fuentes, G.G., E-mail: gfuentes@ain.e [Center of Advanced Surface Engineering, AIN, Cordovilla-Pamplona, E-31191 (Spain); Esparza, J.; Rodriguez, R.J. [Center of Advanced Surface Engineering, AIN, Cordovilla-Pamplona, E-31191 (Spain); Manso-Silvan, M. [Departamento de Fisica Aplicada, Universidad Autonoma de Madrid, Cantoblanco, E-28049 (Spain); Palomares, J. [Instituto de Ciencia de Materiales de Madrid, ICMM-CSIC, Cantoblanco, E-28049 (Spain); Juhasz, J.; Best, S. [Cambridge Centre for Medical Materials, Department of Materials Science and Metallurgy, University of Cambridge, Pembroke Str, Cambridge CB2 3QZ (United Kingdom); Mattilla, R.; Vallittu, P. [Institute of Dentistry, Turku Clinical Biomaterials Centre, Itaeinen Pitkaekatu 4, B FI-20520, Turku (Finland); Achanta, S. [Falex Tribology Wingepark 23 B, 3110 Rotselaar (Belgium); Giazzon, M.; Weder, G. [Centre Suisse d' Electronique et de Microtechnique, CSEM, Jaquet-Drot 1, CH-2002 Neuchatel (Switzerland); Donati, I. [Department of Life Sciences, University of Trieste, Via Licio Giorgieri 1, I 34127 Trieste (Italy)

    2011-01-15

    This work reports on the surface characterisation of 2,2-bis[4-(2-hydroxy-3-methacryloxyl-oxypropoxy)phenyl]propane/triethylene glycol dimethacrylate bio-compatible resins after high energy He{sup +} ion implantation treatments. The samples have been characterised by diffuse reflectance FT-IR, X-ray photo-electron spectroscopy, ultramicro-hardness and nano-scratch wear tests. In addition, osteblast cell assays MG-63 have been used to test the bio-compatibility of the resin surfaces after the ion implantation treatments. It has been observed that the maximum surface hardening of the resin surfaces is achieved at He-ion implantation energies of around 50 keV and fluences of 1 x 10{sup 16} cm{sup -2}. At 50 keV of He-ion bombardment, the wear rate of the resin surface decreases by a factor 2 with respect to the pristine resin. Finally, in vitro tests indicate that the He-ion implantation does not affect to the cell-proliferation behaviour of the UV-cured resins. The enhancement of the surface mechanical properties of these materials can have beneficial consequences, for instance in preventing wear and surface fatigue of bone-fixation prostheses, whose surfaces are continuously held to sliding and shearing contacts of sub-millimetre scale lengths.

  16. U3O8 powder from uranyl-loaded cation exchange resin

    International Nuclear Information System (INIS)

    Mosley, W.C.

    1985-01-01

    Large batches of U 3 O 8 , suitable for powder metallurgy fabrication of Al-U 3 O 8 cores for reactor fuel tubes, have been produced by deep-bed calcination of granular uranyl-loaded macroporous sulfonate cation exchange resin at 900 to 950 0 C in air. Deep-bed calcination is the backup process for the reference process of rotary calcination and sintering. These processes are to be used for recycling uranium, and to produce U 3 O 8 in the Fuel Production Facility to be built at the Savannah River Plant. 2 refs., 6 figs

  17. Dry well conductivity monitoring report for Tanks W-8, W-9, and W-10, Oak Ridge National Laboratory, Oak Ridge, Tennessee

    International Nuclear Information System (INIS)

    1997-10-01

    A treatability study and waste removal program are being implemented for the Gunite ad Associated Tanks Operable Unit at Oak Ridge National Laboratory, Oak Ridge, Tennessee. This report documents the instrumentation and monitoring efforts to establish baseline conductivity conditions. The simulated liquid release (SLR) testing reported here demonstrates the effectiveness of the Conductivity-monitoring method (CMM) as a liquid-release detection method for consolidation Tanks W-8 and W-9 and Tank W-10 in the South Tank Farm (STF). The results show the remarkable sensitivity of the CMM to even very small simulated releases from the tank. The SLR testing for DW-8, DW-9 and DW-10 show that the dry well conductivity monitoring will be effective in detecting potential releases from the tanks during waste removal operations. The data in this report also make clear statements about the inferred integrity of the tanks, tank pads, and drain system: (1) the data substantiate earlier work and show that Tanks W-8, W-9, and W-10 are not leaking; (2) the data show that the pads under Tanks W-8, W-9, and W-10 are integral and connected to the dry wells; (3) the STF drain system appears to be functioning properly. This report presents these results and describes the release monitoring plan for the consolidation tanks and during waste removal operations at all of the tanks in the STF

  18. Design, performance and economics of the DAF Indal 50 kW and 375 kW vertical axis wind turbine

    Science.gov (United States)

    Schienbein, L. A.; Malcolm, D. J.

    1982-03-01

    A review of the development and performance of the DAF Indal 50 kW vertical axis Darrieus wind turbines shows that a high level of technical development and reliability has been achieved. Features of the drive train, braking and control systems are discussed and performance details are presented. A description is given of a wind-diesel hybrid presently being tested. Details are also presented of a 375 kW VAWT planned for production in late 1982. A discussion of the economics of both the 50 kW and 375 kW VAWTs is included, showing the effects of charge rate, installed cost, operating cost, performance and efficiency. The energy outputs are translated into diesel fuel cost savings for remote communities.

  19. Thermo-mechanical tests on W7-X current lead flanges

    International Nuclear Information System (INIS)

    Dhard, Chandra Prakash; Rummel, Thomas; Zacharias, Daniel; Bykov, Victor; Moennich, Thomas; Buscher, Klaus-Peter

    2013-01-01

    Highlights: • There are significant mechanical loads on the cryostat and radial flanges for W7-X current leads. • These are due to evacuation of W7-X cryostat, cool-down of cold mass, electro-magnetic forces and self weight of leads. • The actual mechanical loads were reduced to simplify the experimental set-up. • The tests were carried out on mock-up flanges test assembly at ambient temperature and at 77 K. • The thermo-mechanical tests on W7-X current lead flanges validate the design and joints of these flanges to the leads. -- Abstract: Fourteen pieces of high temperature superconducting current leads (CL) arranged in seven pairs, will be installed on the outer vessel of Wendelstein 7-X (W7-X) stellarator. In order to support the CL, it is provided with two glass fiber reinforce plastic (GFRP) flanges, namely, the lower cryostat flange (CF) remaining at room temperature and upper radial flange (RF) at about 5 K. Both the flanges i.e. CF and RF experience high mechanical loads with respect to the CL, due to the evacuation of W7-X cryostat, cool-down of cold mass including the CL, electro-magnetic forces due to current and plasma operations and self weight of CL. In order to check the integrity of these flanges for such mechanical loads, thermo-mechanical tests were carried out on these flanges at room temperatures and at liquid nitrogen (LN2) temperatures. The details of test set-up, results and modeling are described in the paper

  20. On symmetry hierarchy and radiative corrections in the grand unified model SU(8)sub(L)xSU(8)sub(R)

    International Nuclear Information System (INIS)

    Pirogov, Yu.F.

    1982-01-01

    In the model of precocious chiral unification SU(8)sub(L)xSU(8)sub(R) radiative corrections are calculated for the effective parameters sin 2 thetaw(μ) and α(μ) and the unification mass M 8 is determifed in presence of a hierarchy of intermediate symmetries. The one-loop approximation is used and contributions from the Higgs fields are neglected. It is shown that a natural hierarchy exists leading to a decrease of sinsup(2)thetasub(w)(Msub(wsub(L))) up to sinsup(2)thetasub(w)=1/5-1/4 together with a decrease of M 8 up to M 8 =10 6 -10 7 GeV, as compared with the magnitudes without the hierarchy [ru

  1. Synthesis, structural and microwave dielectric properties of Al2W3-xMoxO12 (x = 0-3) ceramics

    International Nuclear Information System (INIS)

    Surjith, A.; James, Nijesh K.; Ratheesh, R.

    2011-01-01

    Highlights: → Solid state synthesis of phase pure Al 2 W 3-x Mo x O 12 (x = 0-3) compositions. → Sintering studies of Al 2 W 3-x Mo x O 12 (x = 0-3) ceramics. → Structural and microstructural evaluation using powder X-ray diffraction and SEM studies. → Microwave dielectric property evaluation of Al 2 W 3-x Mo x O 12 (x = 0-3) ceramics through Hakki and Coleman post resonator and cavity perturbation techniques. → Structure-property correlation through Laser Raman studies. - Abstract: Low dielectric ceramics in the Al 2 W 3-x Mo x O 12 (x = 0-3) system have been prepared through solid state ceramic route. The phase purity of the ceramic compositions has been studied using powder X-ray diffraction (XRD) studies. The microstructure of the sintered ceramics was evaluated by Scanning Electron Microscopy (SEM). The crystal structure of the ceramic compositions as a result of Mo substitution has been studied using Laser Raman spectroscopy. The microwave dielectric properties of the ceramics were studied by Hakki and Coleman post resonator and cavity perturbation techniques. Al 2 Mo x W 3-x O 12 (x = 0-3) ceramics exhibited low dielectric constant and relatively high unloaded quality factor. The temperature coefficient of resonant frequency of the compositions is found to be in the range -41 to -72 ppm/deg. C.

  2. Studies on dielectric properties, opto-electrical parameters and electronic polarizability of thermally evaporated amorphous Cd{sub 50}S{sub 50x}Se{sub x} thin films

    Energy Technology Data Exchange (ETDEWEB)

    Hassanien, Ahmed Saeed, E-mail: a.s.hassanien@gmail.com [Engineering Mathematics and Physics Department, Faculty of Engineering (Shoubra), Benha University (Egypt); Physics Department, Faculty of Science and Humanities in Ad-Dawadmi, Shaqra University, 11911 (Saudi Arabia)

    2016-06-25

    The objective of this work is to study the influence of the addition of more Se on dielectric properties, opto-electrical parameters and electronic polarizability of amorphous chalcogenide Cd{sub 50}S{sub 50x}Se{sub x} thin films (30 ≤ x50 at%). Thin films of thickness 200 nm were synthesized by vacuum deposition at ≈8.2 × 10{sup −4} Pa. Both refractive index and extinction coefficient were used to obtain all the studied parameters. The high frequency dielectric constant, real and imaginary parts of dielectric constant were discussed. Drude theory was applied to investigate opto-electrical parameters, like optical carrier concentration, optical mobility and optical resistivity. Moreover, other parameters were investigated and studied, e.g. Drude parameters, volume and surface energy loss functions, dielectric loss factor, dielectric relaxation time, complex optical conductivity and electronic polarizability as well as optical electronegativity and third-order nonlinear optical susceptibility. Values of electronic polarizability and nonlinear optical susceptibility were found to be decreased while optical electronegativity increased as Se-content was increased. Increment of Se-content in amorphous Cd{sub 50}S{sub 50x}Se{sub x} thin films has also led to minimize the energy losses when electromagnetic waves propagate through films as well as optical conductivity and the speed of light increased. The other studied properties and parameters of Cd{sub 50}S{sub 50x}Se{sub x} films were found to be strongly dependent upon Se-content. - Highlights: • Thermally evaporated amorphous Cd{sub 50}S{sub 50x}Se{sub x} (30 ≤ x50) thin films were deposited. • Refractive index and absorption index were used to determine almost all properties. • Dielectric properties, Drude parameters and electronic polarizability were studied. • Addition of more Se to CdSSe matrix led to improve the opto-electrical properties. • New data were obtained and

  3. Nanostructured composites based on carbon nanotubes and epoxy resin for use as radar absorbing materials

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Valdirene Aparecida [Instituto Tecnologico de Aeronautica (ITA), Sao Jose dos Campos, SP (Brazil); Folgueras, Luiza de Castro; Candido, Geraldo Mauricio; Paula, Adriano Luiz de; Rezende, Mirabel Cerqueira, E-mail: mirabelmcr@iae.cta.br [Instituto de Aeronautica e Espaco (IAE), Sao Jose dos Campos, SP (Brazil). Div. de Materiais; Costa, Michelle Leali [Universidade Estadual Paulista Julio de Mesquita Filho (DMT/UNESP), Guaratingueta, SP (Brazil). Dept. de Materiais e Tecnologia

    2013-07-01

    Nanostructured polymer composites have opened up new perspectives for multifunctional materials. In particular, carbon nanotubes (CNTs) present potential applications in order to improve mechanical and electrical performance in composites with aerospace application. The combination of epoxy resin with multi walled carbon nanotubes results in a new functional material with enhanced electromagnetic properties. The objective of this work was the processing of radar absorbing materials based on formulations containing different quantities of carbon nanotubes in an epoxy resin matrix. To reach this objective the adequate concentration of CNTs in the resin matrix was determined. The processed structures were characterized by scanning electron microscopy, rheology, thermal and reflectivity in the frequency range of 8.2 to 12.4 GHz analyses. The microwave attenuation was up to 99.7%, using only 0.5% (w/w) of CNT, showing that these materials present advantages in performance associated with low additive concentrations (author)

  4. [Comparison of surface roughness of nanofilled and microhybrid composite resins after curing and polishing].

    Science.gov (United States)

    Jiang, Hong; Lv, Da; Liu, Kailei; Zhang, Weisheng; Yao, Yao; Liao, Chuhong

    2014-05-01

    To compare the surface roughness of nanofilled dental composite resin and microhybrid composite resins after curing and polishing. A nanofilled composite (Z350) and 4 microhybrid composites (P60, Z250, Spectrum, and AP-X) were fabricated from the lateral to the medial layers to prepare 8 mm×8 mm×5 mm cubical specimens. The 4 lateral surfaces of each specimens were polished with abrasive disks (Super-Snap). Profilometer was used to test the mean surface roughness (Ra) after polishing. P60 had the lowest Ra (0.125∓0.030 µm) followed by Z250 and Spectrum. The Ra of Z350 (0.205∓0.052 µm) was greater than that of the other 3 resins, and AP-X had the roughest surfaces. Under scanning electron microscope, the polished faces of P60 resin were characterized by minor, evenly distributed particles with fewer scratches; the polished faces of Z350 presented with scratches where defects of the filling material could be seen. The nanofilled composite Z350 has smooth surface after polishing by abrasive disks, but its smoothness remains inferior to that of other micro-hybrid composite resins.

  5. Development of method to chemical separation of gallium-67 by thermal diffusion technique; Desenvolvimento de metodo para separacao quimica de galio-67 pela tecnica de difusao termica

    Energy Technology Data Exchange (ETDEWEB)

    Martins, Patricia de Andrade

    2012-07-01

    Radioisotopes of gallium have been studied and evaluated for medical applications since 1949. Over the past 50 years {sup 67}Ga has been widely used in the diagnosis of various diseases, including acute and chronic inflammatory lesions, bacterial or sterile and several types of tumors. In Brazil 30% of clinics that provide services for Nuclear Medicine use {sup 67}Ga citrate and the demand for 67{sup G}a at IPEN-CNEN/SP is 37 GBq (1 Ci)/week. The {sup 67}Ga presents physical half-life of 3.26 days (78 hours) and decays 100% by electron capture to stable {sup 67}Zn. Its decay includes the emission of {gamma} rays with energies of 93.3 keV (37%), 184.6 keV (20.4%), 300.2 keV (16.6%) and 888 keV (26%). In the past {sup 67}Ga was produced by the reaction {sup 68}Zn (p, 2n) {sup 67}Ga at IPEN-CNEN/SP. After irradiation, the target was dissolved in concentrated HCl and the solution percolated through a cationic resin DOWEX 50W-X8, 200-400 mesh, conditioned with 10 mol L{sup -1} HCl. Zinc, nickel and copper were eluted in 10 mol L{sup -1} HCl and {sup 67}Ga 3.5 mol L{sup -1} HCl. The final product was obtained as {sup 67}Ga citrate. This work presents a new, fast, direct and efficient method for the chemical separation of 67{sup G}a by thermal diffusion (heating of the target) combined with concentrated acetic acid extraction. Purification was performed by ion exchange chromatography. Natural zinc electrodeposition was performed on nickel/copper plates as substrate and the zinc deposits were adherent to the substrate, slightly shiny and uniform. The targets were irradiated with 26 MeV protons and integrated current of 10 {mu}A.h. After irradiation, the targets were heated at 300 deg C for 2 hours and placed in contact with concentrated acetic acid for 1 hour. The average yield of extraction of {sup 67}Ga was (72 {+-} 10)%. This solution was evaporated and the residue was taken up in 0.5 mol L{sup -1} NH{sub 4}OH. The 67{sup G}a was purified on cationic resin Dowex 50WX8

  6. Electrochemical synthesis, structure and phase composition of nano structured amorphous thin layers of NiW and Ni-Mo

    International Nuclear Information System (INIS)

    Vitina, I.; Lubane, M.; Belmane, V.; Rubene, V.; Krumina, A.

    2006-01-01

    Full text: Nano structured Ni-W thin layers containing W 6-37 wt.% were electrodeposited on a copper substratum. The W content in the layer changes, and it is determined by the electrolyte pH in the range 8.0-9.6 and the cathode current density in the range 1.0-10.0 A/dm 2 . The atomic composition and thermal stability of structure of the electrodeposited thin layers depend for the most part on the conditions of the electrodeposition and less on the W content in the layer. Cracking of the Ni-W layers electrodeposited at the electrolyte pH 8.5 and containing 34-37 wt.% W and 8.5 wt.% W was observed. The cracking increases at heating at 400 deg C for 50 h. On the contrary, no cracking of the Ni-W layer electrodeposited at the electrolyte pH 9.0 and containing 25 wt.% W was observed. The atomic composition of the layer remains practically unchanged at heating at 400 deg C for 50 h. The layer binds oxygen up to 7 wt.%. According to X-ray diffraction, in spite of the W content 35-37 wt.% in the layer, nano structured layers rather than amorphous layers were obtained which at heating at 400 deg C depending on the W content crystallises as Ni or intermetallic compounds Ni x W y if the W content is approx. 25 wt.%. Amorphous Ni-Mo alloys containing 35-52 wt.% Mo was electrodeposited on copper substratum at the cathode current densities of 0.5-1.5 A/dm2 and the electrolyte pH 6.8-8.6. Formation of thin layer (∼1-2μm) of X-ray amorphous Ni-Mo alloy, the Mo content, the characteristics of structure depend on the electrodeposition process, the electrolyte pH, and the cathode current density. The Ni-Mo layer deposited at the electrolyte pH above 8.6 and below average 6.8 had a nanocrystalline structure rather than characteristics of amorphous structure. Ni- W and Ni-Mo alloys were electrodeposited from citrate electrolyte not containing ammonium ions

  7. Formulation and cytotoxicity evaluation of new self-emulsifying multiple W/O/W nanoemulsions

    Directory of Open Access Journals (Sweden)

    Sigward E

    2013-02-01

    Full Text Available Estelle Sigward,1 Nathalie Mignet,1 Patrice Rat,2 Mélody Dutot,2 Saleh Muhamed,1 Jean-Michel Guigner,3 Daniel Scherman,1 Denis Brossard,1 Sylvie Crauste-Manciet11Chemical, Genetic and Imaging Pharmacology Laboratory; INSERM U1022, CNRS UMR8151, Chimie ParisTech, Faculty of Pharmacy, Paris Descartes University, Sorbone Paris Cité, Paris, France; 2Chemistry-Cellular and Analytical Toxicology Laboratory (C-TAC, Faculty of Pharmacy, Paris Descartes University, Sorbone Paris Cité, Paris, France; 3Institut de Minéralogie et de Physique des Milieux Condensés IMPMC -IRD-CNRS UMR 7590, Université Paris Pierre et Marie Curie, Paris, FranceAbstract: Three multiple water-in-oil-in-water (W/O/W nanoemulsions have been designed for potential inclusion of either lipophilic or hydrophilic drugs using a two-step emulsification process exclusively based on low-energy self-emulsification. The W/O primary emulsion was constituted by a blend of oil (medium chain triglyceride, a mixture (7:3 of two surfactants, and a 10% water phase. The surfactants were a mixture of Polysorbate-85/Labrasol®, Polysorbate-85/ Cremophor® EL or glycerol/Polysorbate-85. The final W/O/W nanoemulsions were obtained by the addition of water, with a weight ratio nanoemulsion/water of 1:2. The multiple emulsion stability was found to increase from 24 hours to 2 and 6 months with Labrasol, glycerol, and Cremophor, respectively. Cytotoxicity was found for formulations including Labrasol and Cremophor EL. The concentration of emulsion inhibiting 50% cell viability (IC50 was determined using the alamarBlue® test, giving after 24 hours of incubation, IC50 = 10.2 mg/mL for the Labrasol formulation and IC50 = 11.8 mg/mL for the Cremophor EL formulation. Corresponding calculated IC50 values for surfactants were 0.51 mg/mL for Labrasol and 0.59 mg/mL for Cremophor EL. In both cases, cytotoxicity was due to an apoptotic mechanism, evidenced by chromatin condensation and P2X7 cell death

  8. The determination of molybdenum and tungsten in resin by x-ray-fluorescence spectrometry

    International Nuclear Information System (INIS)

    Eddy, B.T.

    1985-01-01

    This report describes a method using X-ray-fluorescence spectrometry for the determination of molybdenum and tungsten in ion-exchange resins. The dried resin is milled with sand, binder, and an internal-standard mixture before being briquetted. Niobium and zinc are used as the internal standards for molybdenum and tungsten respectively. Intensity measurements are made with the gold anode tube. Corrections are made for the interference of the Mo Kα analytical line on the background intensities used for the Mo Kα and Nb Kα lines. The precision of the analysis for molybdenum ranges from a relative standard deviation 0,02 at 5 mg/g to 0.045 at 55μg/g; for tungsten, the relative standard deviation ranges from 0,04 at 5 mg/g to 0,055 at 55μg/g. The limits of determination in the original resin sample were found to be 40μg/g for molybdenum and 80μg/g for tungsten. The laboratory method is given in an appendix

  9. Phase transitions and electrical properties of Bi2W1−xNbxO6−y and Bi2W1−xTaxO6−y

    International Nuclear Information System (INIS)

    Kharitonova, E.P.; Voronkova, V.I.; Gagor, A.B.; Pietraszko, A.P.; Alekseeva, O.A.

    2013-01-01

    Highlights: •The limit of Bi 2 W 1−x Me x O 6−y solid solutions is at x = 0.1, 0.15 for Me = Nb, Ta. •Ta and Nb substitutions for W suppress the reconstructive phase transition. •Bi 2 W 0.9 Nb 0.1 O 6−y samples belong to Aurivillius-type structure up to their melting. •Nb and Ta doping shifts ferroelectric transition to low temperatures up to 200 °C. •The highest conductivity reaches 10 −1 S/cm at 800 °C (x = 0.05, 0.1; Me = Nb, Ta). -- Abstract: Polycrystalline samples of Bi 2 W 1−x Me x O 6−y (Me = Nb, Ta) solid solutions have been prepared by solid-state reactions, and the influence of Nb and Ta substitutions for W on the polymorphism and electrical properties of Bi 2 WO 6 has been studied. The limit of the solid solutions is at x = 0.1 for Me = Nb and at x = 0.15 for Me = Ta. The distinctive features of the polymorphism of the Nb- and Ta-doped materials have been identified. According to differential scanning calorimetry data, tantalum and niobium substitutions for tungsten increase the temperature of the high-temperature, orthorhombic-to-monoclinic reconstructive phase transition and suppress the transition starting at x = 0.05 for Me = Nb and x = 0.10 for Me = Ta. As a result, the Bi 2 W 1−x Nb x O 6−y samples have an orthorhombic Aurivillius-type structure up to their melting point. The Bi 2 W 1−x Ta x O 6−y solid solutions at high temperatures consist of a mixture of an orthorhombic and a monoclinic phase. Nb and Ta doping shifts the ferroelectric phase transition to lower temperatures by more than 200 °C, thus markedly extending the stability range of the nonpolar orthorhombic paraelectric phase, which exists in a temperature range as narrow as 930–960 °C in the case of undoped Bi 2 WO 6 . The increase in oxygen vacancy concentration due to heterovalent substitutions of Nb 5+ and Ta 5+ for W 6+ leads to an increase in conductivity by two orders of magnitude relative to the unsubstituted compound

  10. Purification of cyclotron-produced 81Rb for the preparation of small krypton-81m generators

    International Nuclear Information System (INIS)

    Andersen, P.; Haasbroek, F.J.; Venter, S.S.J.; Strelow, F.W.E.

    1981-01-01

    A method is described for the separation of 81 Rb from sodium bromide targets. Ammonium molybdophosphate columns are used and the separation takes only about 20 minutes. More than 90% of the 81 Rb is recovered. The purified 81 Rb enables small Rubidium-81/Krypton-81m generators to be prepared with Bio-Rad 50W-X8 ion-exchange resin (200-400 mesh) [af

  11. A Fourier transform Raman spectroscopy analysis of the degree of conversion of a universal hybrid resin composite cured with light-emitting diode curing units.

    Science.gov (United States)

    Lindberg, Anders; Emami, Nazanin; van Dijken, Jan W V

    2005-01-01

    The degree of conversion (DC), of a universal hybrid resin composite cured with LED curing units with low and high power densities and a 510 mW/cm2 quartz tungsten halogen unit, was investigated with Fourier Transform Raman spectroscopy. Three curing depths (0, 2, 4mm) and 0 and 7 mm light guide tip - resin composite (LT - RC) distances were tested. The DC of the LED units varied between 52.3% - 59.8% at the top surface and 46.4% - 57.0% at 4 mm depth. The DC of specimen cured with a 0 mm LT- RC distance at 4 mm depth varied between 50.8% - 57.0% and with 7 mm distance between 46.4% - 55.4%. The low power density LED unit showed a significantly lower DC for both distances at all depth levels compared to the other curing units (p units were only found at the 4 mm depth level cured from 7 mm distance (p units. It can be concluded that the improved LED curing units could cure the studied resin composite to the same DC as the control unit.

  12. Influence of energy density of different light sources on knoop hardness of a dual-cured resin cement

    Directory of Open Access Journals (Sweden)

    Evandro Piva

    2008-06-01

    Full Text Available The purpose of this study was to evaluate the Knoop hardness of a dual-cured resin-based luting cement irradiated with different light sources as well energy density through a ceramic sample. Three light-curing unit (LCUs were tested: tungsten halogen light (HAL, light-emitting diode (LED and xenon plasma-arc (PAC lamp. Disc-shaped specimens were fabricated from a resin-based cement (Enforce. Three energy doses were used by modifying the irradiance (I of each LCU and the irradiation time (T: 24 Jcm-2 (I/2x2T, 24 Jcm-2 (IxT and 48 Jcm-2 (Ix2T. Energy doses were applied through a 2.0-mm-thick ceramic sample (Duceram Plus. Three groups underwent direct irradiation over the resin cement with the different LCUs and a chemically-activated group served as a control. Thirteen groups were tested (n=10. Knoop hardness number (KHN means were obtained from cross-sectional areas. Two-way ANOVA and the Holm-Sidak method were used for statistical comparisons of activation mode and energy doses (a=5%. Application of 48 J.cm-2 energy dose through the ceramic using LED (50.5±2.8 and HAL (50.9±3.7 produced significantly higher KHN means (p<0.05 than the control (44.7±3.8. LED showed statistically similar performance to HAL. Only HAL showed a relationship between the increase of LCU energy dose and hardness increase.

  13. Influence of energy density of different light sources on Knoop hardness of a dual-cured resin cement.

    Science.gov (United States)

    Piva, Evandro; Correr-Sobrinho, Lourenço; Sinhoreti, Mario Alexandre Coelho; Consani, Simonides; Demarco, Flávio Fernando; Powers, John Michael

    2008-01-01

    The purpose of this study was to evaluate the Knoop hardness of a dual-cured resin-based luting cement irradiated with different light sources as well energy density through a ceramic sample. Three light-curing unit (LCUs) were tested: tungsten halogen light (HAL), light-emitting diode (LED) and xenon plasma-arc (PAC) lamp. Disc-shaped specimens were fabricated from a resin-based cement (Enforce). Three energy doses were used by modifying the irradiance (I) of each LCU and the irradiation time (T): 24 Jcm(-2) (I/2x2T), 24 Jcm(-2) (IxT) and 48 Jcm(-2) (Ix2T). Energy doses were applied through a 2.0-mm-thick ceramic sample (Duceram Plus). Three groups underwent direct irradiation over the resin cement with the different LCUs and a chemically-activated group served as a control. Thirteen groups were tested (n=10). Knoop hardness number (KHN) means were obtained from cross-sectional areas. Two-way ANOVA and the Holm-Sidak method were used for statistical comparisons of activation mode and energy doses (alpha=5%). Application of 48 J.cm(-2) energy dose through the ceramic using LED (50.5+/-2.8) and HAL (50.9+/-3.7) produced significantly higher KHN means (p<0.05) than the control (44.7+/-3.8). LED showed statistically similar performance to HAL. Only HAL showed a relationship between the increase of LCU energy dose and hardness increase.

  14. Feasibility of a Heavy Ion Beam Probe for W7-X

    Science.gov (United States)

    Crowley, T. P.; Demers, D. R.; Fimognari, P. J.; Grulke, O.; Laube, R.

    2017-10-01

    A feasibility study of a Heavy Ion Beam Probe (HIBP) diagnostic for the Wendelstein 7-X (W7-X) superconducting stellarator, incorporating the accelerator and energy analyzer (currently in Greifswald) from the 2 MeV TEXT-U HIBP, is being carried out. The study's results are positive: beam trajectory simulations in the W7-X standard magnetic configuration, with central densities up to 1020 m-3, predict that it will be possible to measure the equilibrium plasma potential and Er at all radii, and simultaneously measure temporally and spatially resolved fluctuations of ne and potential for r / a >0.5. This will provide a unique capability to advance understanding of neoclassical and turbulent particle and energy transport in W7-X. Within this feasibility study, the beam is injected and detected through the K11 and N11 ports respectively, and the toroidal magnetic field is in the ` + φ ' direction. Additional beam simulations reveal that most radii can be accessed in 7 other paradigm magnetic configurations. It's anticipated that electrostatic beam steering suitable for studying all these configurations is plausible; it will have plate dimensions comparable to TEXT-U's with smaller electric fields and higher voltages. Initial estimates of anticipated heat load from the W7-X plasma on the steering systems indicate it will be significant, but tractable. Our conclusion from these studies is that an HIBP diagnostic for W7-X is feasible. This work is supported by US DoE Award DE-SC0013918.

  15. Ag@Ag_8W_4O_1_6 nanoroasted rice beads with photocatalytic, antibacterial and anticancer activity

    International Nuclear Information System (INIS)

    Selvamani, Muthamizh; Krishnamoorthy, Giribabu; Ramadoss, Manigandan; Sivakumar, Praveen Kumar; Settu, Munusamy; Ranganathan, Suresh; Vengidusamy, Narayanan

    2016-01-01

    Increasing resistance of pathogens and cancer cell line towards antibiotics and anticancer agents has caused serious health problems in the past decades. Due to these problems in recent years, researchers have tried to combine nanotechnology with material science to have intrinsic antimicrobial and anticancer activity. The metals and metal oxides were investigated with respect to their antimicrobial and anticancer effects towards bacteria and cancer cell line. In the present work metal@metal tungstate (Ag@Ag_8W_4O_1_6 nanoroasted rice beads) is investigated for antibacterial activity against Escherichia coli and Staphylococcus aureus using Mueller-Hinton broth and the anticancer activity against B16F10 cell line was studied. Silver decorated silver tungstate (Ag@Ag_8W_4O_1_6) was synthesized by the microwave irradiation method using Cetyl Trimethyl Ammonium Bromide (CTAB). Ag@Ag_8W_4O_1_6 was characterized by using various spectroscopic techniques. The phase and crystalline nature were analyzed by using XRD. The morphological analysis was carried out using Field Emission Scanning Electron Microscopy (FE-SEM), and High Resolution Transmission Electron Microscopy (HR-TEM). Further, Fourier Transform Infrared Spectroscopy (FT-IR) and Raman spectral analysis were carried out in order to ascertain the presence of functional groups in Ag@Ag_8W_4O_1_6. The optical property was investigated using Diffuse Reflectance Ultraviolet–Visible Spectroscopy (DRS-UV–Vis) and the band gap was found to be 3.08 eV. Surface area of the synthesized Ag@Ag_8W_4O_1_6 wasanalyzed by BET analysis and Ag@Ag_8W_4O_1_6 was utilized for the degradation of organic dyes methylene blue and rhodamine B. The morphology of the Ag@Ag_8W_4O_1_6 resembles roasted rice beads with breath and length in nm range. The oxidation state of tungsten (W) and silver (Ag) was investigated using X-ray photoelectron spectroscopy (XPS). - Highlights: • Synthesis of Ag@Ag_8W_4O_1_6 nanoroasted rice beads using

  16. Posterior bulk-filled resin composite restorations.

    DEFF Research Database (Denmark)

    van Dijken, Jan WV; Pallesen, Ulla

    2016-01-01

    up to 4mm as needed to fill the cavity 2mm short of the occlusal cavosurface. The occlusal part was completed with the nano-hybrid resin composite (Ceram X mono+). In the other cavity, the resin composite-only (Ceram X mono+) was placed in 2mm increments. The restorations were evaluated using...... Class II, 4 SDR-CeramX mono+ and 6 CeramXmono+-only restorations. The main reasons for failurewere tooth fracture (6) and secondary caries (4). The annual failure rate (AFR) for all restorations (Class I and II) was for the bulk-filled-1.1% and for the resin composite-only restorations 1...

  17. OBLICZENIE PRZEPŁYWÓW MAKSYMALNYCH I ICH REDUKCJI W ZLEWNI ZURBANIZOWANEJ

    Directory of Open Access Journals (Sweden)

    Mariusz BARSZCZ

    2016-03-01

    Full Text Available W pracy przedstawiono wyniki zastosowania modelu SWMM do obliczenia przepływów o prawdopodobieństwach 50, 10, 2 i 1% w 8. przekrojach Potoku Służewieckiego na odcinku od km 0+000 do 6+576 oraz w 2. przekrojach Rowu Wolica. Zlewnia Potoku Służewieckiego jest zlokalizowana w południowej części Warszawy. Największe zagrożenie powodziowe występuje na odcinku Potoku Służewieckiego od km 0+000 do 3+875. Przepustowość koryta Potoku na tym odcinku kształtuje się na poziomie przepływu maksymalnego o prawdopodobieństwie 50%. Największe wartości przepływów w Potoku Służewieckim prognozowano w przekroju obliczeniowym numer V (km 4+267: Q50% = 13,863, Q10% = 23,019, Q2% = 28,825 i Q1% = 30,500 m3·s-1. Jedną z przyczyn występowania zagrożenia powodziowego w dolnym biegu Potoku Służewieckiego jest dopływ dużej ilości wód opadowych Rowem Wolica. Wartości przepływów w górnym odcinku Rowu Wolica (w przekroju VI zawierały się w granicach od 8,005 do 12,402 m3·s-1, w zależności od prawdopodobieństwa wystąpienia opadu obliczeniowego. W celu określenia możliwości redukcji przepływów w Rowie Wolica, przeprowadzono obliczenia w których uwzględniono zastosowanie kryzy na odcinku ujściowym kolektora do kanału otwartego. Zastosowanie kryzy w kolektorze pozwoli zredukować przepływy o prawdopodobieństwach 50, 10 i 2% odpowiednio o 61,0; 46,0 i 36,6%. Zastosowanie kryzy o stałej średnicy ϕ1,08 m, ustalonej dla przepływu o prawdopodobieństwie 2%, spowoduje znacznie mniejszą redukcję przepływów maksymalnych o prawdopodobieństwach 50 i 10%.

  18. Spent 99Mo/99mTc generator as an economical source of 99Mo

    International Nuclear Information System (INIS)

    El-Kolaly, M.T.

    1990-01-01

    An improved method for utilization and purification of 99 Mo from spent 90 Mo/ 99m Tc generators has been described. After washing the generator with saline to remove the generated 99m Tc, followed by 2 mL 5 M NaOH containing a few drops of H 2 O 2 , the 99 Mo was quantitatively eluted from the generator with 5 mL 5 M NaOH. The alkaline eluate containing 99 Mo was contaminated with partially dissolved alumina. In the present method, an anion-exchange resin Dowex 1 x 8 column was used for purification of 99 Mo from the contaminating alumina. The resultant 99 Mo was of high purity and contained 3+ /mL 99 Mo solution, as estimated by atomic absorption. (author)

  19. Design and assembly technology for the thermal insulation of the W7-X cryostat

    Energy Technology Data Exchange (ETDEWEB)

    Risse, K., E-mail: konrad.risse@ipp.mpg.de [Max-Planck-Institut fuer Plasmaphysik (IPP), Euratom Association, Wendelsteinstrasse 1, D-17491 Greifswald (Germany); Nagel, M.; Pietsch, M.; Braatz, A. [Max-Planck-Institut fuer Plasmaphysik (IPP), Euratom Association, Wendelsteinstrasse 1, D-17491 Greifswald (Germany); Binni, A. [MAN Diesel and Turbo SE, Dpt. OSA, Werftstrasse 17, D-94469 Deggendorf (Germany); Posselt, H. [Linde AG Engineering Div., Dr.-Carl-von-Linde-Strasse 6-14, D-82049 Hoellriegelskreuth (Germany)

    2011-10-15

    The Max-Planck-Institut fuer Plasmaphysik in Greifswald is building up the stellarator fusion experiment Wendelstein 7-X (W7-X). To operate the superconducting magnet system the vacuum and the cold structures are protected by a thermal insulated cryostat. The plasma vessel forms the inner cryostat wall, the outer wall is realised by a thermal insulated outer vessel. In addition 254 thermal insulated ports are fed through the cryogenic vacuum to allow the access to the plasma vessel for heating systems, supply lines or plasma diagnostics. The thermal insulation is being manufactured and assembled by MAN Diesel and Turbo SE (Germany). It consists of a multi-layer insulation (MLI) made of aluminized Kapton with a silk like fibreglass spacer and a thermal shield covering the inner cryostat surfaces. The shield on the plasma vessel is made of fibreglass reinforced epoxy resin with integrated copper meshes. The outer vessel insulation is made of brass panels with an average size of 3.3 x 2.0 m{sup 2}. Cooling loops made of stainless steel are connected via copper strips to the brass panels. Especially the complex 3 D shape of the plasma vessel, the restricted space inside the cryostat and the consideration of the operational component movements influenced the design work heavily. The manufacturing and the assembly has to fulfil stringent geometrical tolerances e.g. for the outer vessel panels +3/-2 mm.

  20. Design and assembly technology for the thermal insulation of the W7-X cryostat

    International Nuclear Information System (INIS)

    Risse, K.; Nagel, M.; Pietsch, M.; Braatz, A.; Binni, A.; Posselt, H.

    2011-01-01

    The Max-Planck-Institut fuer Plasmaphysik in Greifswald is building up the stellarator fusion experiment Wendelstein 7-X (W7-X). To operate the superconducting magnet system the vacuum and the cold structures are protected by a thermal insulated cryostat. The plasma vessel forms the inner cryostat wall, the outer wall is realised by a thermal insulated outer vessel. In addition 254 thermal insulated ports are fed through the cryogenic vacuum to allow the access to the plasma vessel for heating systems, supply lines or plasma diagnostics. The thermal insulation is being manufactured and assembled by MAN Diesel and Turbo SE (Germany). It consists of a multi-layer insulation (MLI) made of aluminized Kapton with a silk like fibreglass spacer and a thermal shield covering the inner cryostat surfaces. The shield on the plasma vessel is made of fibreglass reinforced epoxy resin with integrated copper meshes. The outer vessel insulation is made of brass panels with an average size of 3.3 x 2.0 m 2 . Cooling loops made of stainless steel are connected via copper strips to the brass panels. Especially the complex 3 D shape of the plasma vessel, the restricted space inside the cryostat and the consideration of the operational component movements influenced the design work heavily. The manufacturing and the assembly has to fulfil stringent geometrical tolerances e.g. for the outer vessel panels +3/-2 mm.

  1. Antibacterial effect of composite resins containing quaternary ammonium polyethyleneimine nanoparticles

    International Nuclear Information System (INIS)

    Yudovin-Farber, Ira; Beyth, Nurit; Weiss, Ervin I.; Domb, Abraham J.

    2010-01-01

    Quaternary ammonium polyethyleneimine (QA-PEI)-based nanoparticles were synthesized by crosslinking with dibromopentane followed by N-alkylation with various alkyl halides and further N-methylation with methyl iodide. Insoluble pyridinium-type particles were prepared by suspension polymerization of 4-vinyl pyridine followed by N-alkylation with alkyl halides. Polyamine-based nanoparticles embedded in restorative composite resin at 1% w/w were tested for antibacterial activity against Streptococcus mutans using direct contact test. Activity analysis revealed that the alkyl chain length of the QA-PEI nanoparticles plays a significant role in antibacterial activity of the reagent. The most potent compound was octyl-alkylated QA-PEI embedded in restorative composite resin at 1% w/w that totally inhibited S. mutans growth in 3-month-aged samples. This data indicates that restorative composite resin with antibacterial properties can be produced by the incorporation of QA-PEI nanoparticles.

  2. Antibacterial effect of composite resins containing quaternary ammonium polyethyleneimine nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Yudovin-Farber, Ira [Hebrew University of Jerusalem, Department of Medicinal Chemistry and Natural Products, School of Pharmacy, Faculty of Medicine (Israel); Beyth, Nurit; Weiss, Ervin I. [Hebrew University of Jerusalem, Department of Prosthodontics, Faculty of Dentistry (Israel); Domb, Abraham J., E-mail: avid@ekmd.huji.ac.i [Hebrew University of Jerusalem, Department of Medicinal Chemistry and Natural Products, School of Pharmacy, Faculty of Medicine (Israel)

    2010-02-15

    Quaternary ammonium polyethyleneimine (QA-PEI)-based nanoparticles were synthesized by crosslinking with dibromopentane followed by N-alkylation with various alkyl halides and further N-methylation with methyl iodide. Insoluble pyridinium-type particles were prepared by suspension polymerization of 4-vinyl pyridine followed by N-alkylation with alkyl halides. Polyamine-based nanoparticles embedded in restorative composite resin at 1% w/w were tested for antibacterial activity against Streptococcus mutans using direct contact test. Activity analysis revealed that the alkyl chain length of the QA-PEI nanoparticles plays a significant role in antibacterial activity of the reagent. The most potent compound was octyl-alkylated QA-PEI embedded in restorative composite resin at 1% w/w that totally inhibited S. mutans growth in 3-month-aged samples. This data indicates that restorative composite resin with antibacterial properties can be produced by the incorporation of QA-PEI nanoparticles.

  3. Overview on resins available in microlithography

    International Nuclear Information System (INIS)

    Serre, B.; Schue, F.; Montginoul, C.; Giral, L.

    1985-01-01

    Lithographic equipments using electrons and X radiation are developed. Velocity and resolution requirements fix the nature of the material to irradiate. Circuit making principles are recalled here; resists (organic polymers) are employed for it. The different types of resins and then needed characteristics are reviewed here. In the scope of electron sensitive resins methyl polymethacrylate and derivative and its copolymers (and copolymers of methacrylonitrile) and reticulated copolymers are studied. Polysulfones are also presented (poly(buten-1 sulfone), poly(styrene sulfone), poly(methyl-1 cyclopentene-1 sulfone). The interest in photosensitive resins (such as AZ) as electron sensitive resins is recalled. In the field of negative resins, the polyepoxyds, polystyrene and halogenated derivates from polystyrene (CMS and PCMS), the poly(vinyl-2 naphtalene) and its derivatives (PSTTF) are presented. The X radiation sensitive resins are also reviewed: the methyl polymethacrylate and its halogenated derivates, the acrylic homopolymers and copolymers (example of poly(acrylate of chlorinated alcoyls). The resins developable by plasma are mentioned. At last, for photosensitive resins, the diazide polydiene systems are presented together with systems diazo-2 2H-naphtalenone-1. The systems with salt photolysis are just recalled [fr

  4. Studies Regarding As(V Adsorption from Underground Water by Fe-XAD8-DEHPA Impregnated Resin. Equilibrium Sorption and Fixed-Bed Column Tests

    Directory of Open Access Journals (Sweden)

    Mihaela Ciopec

    2014-10-01

    Full Text Available The characteristics of arsenic adsorption onto Fe-XAD8-DEHPA resin were studied on the laboratory scale using aqueous solutions and natural underground waters. Amberlite XAD8 resin was impregnated with di(2-ethylhexyl phosphoric acid (DEHPA via the dry method of impregnation. Fe(III ions were loaded onto the impregnated resin by exploiting the high affinity of arsenic towards iron. The studies were conducted by both in contact and continuous modes. Kinetics data revealed that the removal of arsenic by Fe-XAD8-DEHPA resin is a pseudo-second-order reaction. The equilibrium data were modelled with Freundlich Langmuir and Dubinin Radushkevich (D-R isotherms and it was found that the Freundlich model give the poorest correlation coefficient. The maximum adsorption capacity obtained from the Langmuir isotherm is 22.6 µg As(V/g of Fe-XAD8-DEHPA resin. The mean free energy of adsorption was found in this study to be 7.2 kJ/mol and the ΔG° value negative (−9.2 kJ/mol. This indicates that the sorption process is exothermal, spontaneous and physical in nature. The studied Fe-XAD8-DEHPA resin showed excellent arsenic removal performance by sorption, both from synthetic solution and the natural water sample, and could be regenerated simply by using aqueous NaOH or HCl solutions.

  5. Quantitative analysis of PMR-15 polyimide resin by HPLC

    Science.gov (United States)

    Roberts, Gary D.; Lauver, Richard W.

    1987-01-01

    The concentration of individual components and of total solids of 50 wt pct PMR-15 resin solutions was determined using reverse-phase HPLC to within + or - 8 percent accuracy. Acid impurities, the major source of impurities in 3,3', 4,4'-benzophenonetetracarboxylic acid (BTDE), were eliminated by recrystallizing the BTDE prior to esterification. Triester formation was not a problem because of the high rate of esterification of the anhydride relative to that of the carboxylic acid. Aging of PMR-15 resin solutions resulted in gradual formation of the mononadimide and bisnadimide of 4,4'-methylenedianiline, with the BTDE concentration remaining constant. Similar chemical reactions occurred at a reduced rate in dried films of PMR-15 resin.

  6. Electron mobility in few-layer MoxW1-xS2

    International Nuclear Information System (INIS)

    Chandrasekar, Hareesh; Nath, Digbijoy N

    2015-01-01

    Heterostructures of two-dimensional (2D) layered materials are increasingly being explored for electronics in order to potentially extend conventional transistor scaling and to exploit new device designs and architectures. Alloys form a key underpinning of any heterostructure device technology and therefore an understanding of their electronic properties is essential. In this paper, we study the intrinsic electron mobility in few-layer Mo x W 1−x S 2 as limited by various scattering mechanisms. The room temperature, energy-dependent scattering times corresponding to polar longitudinal optical (LO) phonon, alloy and background impurity scattering mechanisms are estimated based on the Born approximation to Fermi’s golden rule. The contribution of individual scattering rates is analyzed as a function of 2D electron density as well as of alloy composition in Mo x W 1−x S 2 . While impurity scattering limits the mobility for low carrier densities (<2–4×10 12 cm −2 ), LO polar phonon scattering is the dominant mechanism for high electron densities. Alloy scattering is found to play a non-negligible role for 0.5 < x < 0.7 in Mo x W 1−x S 2 . The LO phonon-limited and impurity-limited mobilities show opposing trends with respect to alloy mole fractions. The understanding of electron mobility in Mo x W 1−x S 2 presented here is expected to enable the design and realization of heterostructures and devices based on alloys of MoS 2 and WS 2 . (paper)

  7. The quaternary arsenide oxides Ce{sub 9}Au{sub 5-x}As{sub 8}O{sub 6} and Pr{sub 9}Au{sub 5-x}As{sub 8}O{sub 6}

    Energy Technology Data Exchange (ETDEWEB)

    Bartsch, Timo; Hoffmann, Rolf-Dieter; Poettgen, Rainer [Univ. Muenster (Germany). Inst. fuer Anorganische und Analytische Chemie

    2016-07-01

    The quaternary gold arsenide oxides Ce{sub 9}Au{sub 5-x}As{sub 8}O{sub 6} and Pr{sub 9}Au{sub 5-x}As{sub 8}O{sub 6} were synthesized from the rare earth elements (RE), rare earth oxides, arsenic and gold powder at maximum annealing temperatures of 1173 K. The structures were refined from single crystal X-ray diffractometer data: Pnnm, a=1321.64(6) pm, b=4073.0(3), c=423.96(2), wR2=0.0842, 3106 F{sup 2} values, 160 variables for Ce{sub 9}Au{sub 4.91(4)}As{sub 8}O{sub 6} and Pnnm, a=1315.01(4), b=4052.87(8), c=420.68(1) pm, wR2=0.0865, 5313 F{sup 2} values, 160 variables for Pr{sub 9}Au{sub 4.75(1)}As{sub 8}O{sub 6}. They represent a new structure type and show a further extension of pnictide oxide crystal chemistry. A complex polyanionic gold arsenide network [Au{sub 5}As{sub 8}]{sup 15-} (with some disorder in the gold substructure) is charge compensated with polycationic strands of condensed edge-sharing O rate at RE{sub 4/4} and O rate at RE{sub 4/3} tetrahedra ([RE{sub 4}O{sub 3}]{sub 2}{sup 12+}) as well as RE{sup 3+} cations in cavities.

  8. A study of w boson decay charge asymmetry using hadronic tau decays in proton - anti-proton collisions at √s = 1.8 TeV

    Energy Technology Data Exchange (ETDEWEB)

    Kuns, Edward William [Rutgers Univ., New Brunswick, NJ (United States)

    1998-01-01

    This dissertation presents a measurement of the tau charge asymmetry in events where the taus are produced by W decays. This charge asymmetry appears as different rapidity distributions for positive and negative taus. Two competing effects generate tau charge asymmetry. The production mechanism for the W gauge boson generates a charge asymmetry which is a function of the ratio of parton distribution functions, d(x)=u(x), measured at x ~ MW/√s. This is the dominant effect for tau charge asymmetry at small rapidity. At higher rapidity, however, the competing charge asymmetry from parity violation in W decay to taus becomes dominant. This tau asymmetry measurement is consistent with the Standard Model with a x2 per degree of freedom equal to 2.5 for 4 degrees of freedom when the asymmetry measurement is folded about y = 0, taking advantage of the CP symmetry of the underlying physics, and 8.9 for 8 degrees of freedom when it is not. This measurement introduces some methods and variables of interest to future analyses using hadronic decay modes of taus. This work was done using the CDF detector in $\\bar{p}$p collisions at √s = 1.8 TeV at Fermilab's Tevatron accelerator.

  9. Atomic layer deposition of W{sub x}N/TiN and WN{sub x}C{sub y}/TiN nanolaminates

    Energy Technology Data Exchange (ETDEWEB)

    Elers, K.-E.; Saanila, V.; Li, W.-M.; Soininen, P.J.; Kostamo, J.T.; Haukka, S.; Juhanoja, J.; Besling, W.F.A

    2003-06-23

    Diffusion barrier materials, such as TiN, W{sub x}N, WN{sub x}C{sub y} and their nanolaminates were deposited by atomic layer deposition method. TiN film exhibited excellent properties, but W{sub x}N film exhibited high resistivity despite the low residue concentration. Both TiN and W{sub x}N films suffered from serious incompatibility with the copper metal. WN{sub x}C{sub y} film was deposited by introducing triethylboron as a reducing agent for tungsten. Excellent film properties were obtained, including very good compatibility with the copper metal, evident as strong adhesion and no pitting on the copper surface. Nanolaminate barrier stacks of W{sub x}N/TiN and WN{sub x}C{sub y}/TiN were successfully deposited. TiN deposition did not cause copper pitting when thin WN{sub x}C{sub y} film was deposited underneath.

  10. Advances In Hexavalent Chromium Removal At Hanford

    International Nuclear Information System (INIS)

    Neshem, D.O.; Riddelle, J.

    2012-01-01

    At the Hanford Site, chromium was used as a corrosion inhibitor in the reactor cooling water and was introduced into the groundwater as a result of planned and unplanned discharges from reactors during plutonium production since 1944. Beginning in 1995, groundwater treatment methods were evaluated leading to the use of pump and treat facilities with ion exchange using Dowex 21 K, a regenerable strong base anion exchange resin. This required regeneration of the resin, which is currently performed offsite. Resin was installed in a 4 vessel train, with resin removal required from the lead vessel approximately once a month. In 2007, there were 8 trains (32 vessels) in operation. In 2008, DOE recognized that regulatory agreements would require significant expansion in the groundwater chromium treatment capacity. Previous experience from one of the DOE project managers led to identification of a possible alternative resin, and the contractor was requested to evaluate alternative resins for both cost and programmatic risk reductions. Testing was performed onsite in 2009 and 2010, using a variety of potential resins in two separate facilities with groundwater from specific remediation sites to demonstrate resin performance in the specific groundwater chemistry at each site. The testing demonstrated that a weak base anion single-use resin, ResinTech SIR-700, was effective at removing chromium, had a significantly higher capacity, could be disposed of efficiently on site, and would eliminate the complexities and programmatic risks from sampling, packaging, transportation and return of resin for regeneration. This resin was installed in Hanford's newest groundwater treatment facility, called 100-DX, which began operations in November, 2010, and used in a sister facility, 100-HX, which started up in September of 2011. This increased chromium treatment capacity to 25 trains (100 vessels). The resin is also being tested in existing facilities that utilize Dowex 21 K for

  11. Leachability of cesium from cemented evaporator concentrates and ion-exchange resins

    International Nuclear Information System (INIS)

    Muurinen, A.

    1985-03-01

    Leachabilities of cesium from cemented evaporator concentrates and ion-exchange resins were measured. The standard draft of the International Organization for Standardization (ISO, 1979) for long-term leach testing was followed in the research. Three resin concretes and three concentrate concretes were tested. Deionized water and groundwater were used as leachants. The leaching temperature was 20-23 deg C. The incremental leach rate at the end of the three and a half year test varied between 5x10 -12 - 15x10 -12 m/s and the cumulative activity fraction leached between 1.5x10 -3 - 6x10 -3 m. The apparent diffusion coefficients in groundwater varied between 10 -9 - 10 -8 m/day. Because of the cracking the specimens cannot, however, be regarded as whole blocks, but the effects of cracking should be taken into account. (author)

  12. Concentrating cesium-137 from seawater using resorcinol-formaldehyde resin for radioecological monitoring

    Energy Technology Data Exchange (ETDEWEB)

    Egorin, Andrei; Tokar, Eduard; Tutov, Mikhail; Avramenko, Valentin [Institute of Chemistry FEBRAS, Vladivostok (Russian Federation); Far Eastern Federal Univ., Vladivostok (Russian Federation); Palamarchuk, Marina; Marinin, Dmitry [Institute of Chemistry FEBRAS, Vladivostok (Russian Federation)

    2017-04-01

    A method of preconcentrating cesium-137 from seawater using a resorcinol-formaldehyde resin, which enables one to optimize the ecological monitoring procedure, has been suggested. Studies of sorption of cesium-137 from seawater by resorcinol-formaldehyde resin have been performed, and it has been demonstrated that the cation exchanger is characterized by high selectivity with respect to cesium-137. It was found that the selectivity depended on the temperature of resin solidification and the seawater pH value. The maximal value of the cesium-137 distribution coefficient is equal to 4.1-4.5 x 10{sup 3} cm{sup 3} g{sup -1}. Under dynamic conditions, the ion-exchange resin capacity is 310-910 bed volumes depending on the seawater pH, whereas the efficiency of cesium removal exceeds 95%. The removal of more than 95% of cesium-137 has been attained using 1-3 M solutions of nitric acid: here, the eluate volume was 8-8.4 bed volumes. Application of 3 M solution of nitric acid results in resin degradation with the release of gaseous products.

  13. Shielding of the NBI boxes against W7-X magnetic stray fields

    Energy Technology Data Exchange (ETDEWEB)

    Kick, Manfred [Max-Planck-Institut fuer Plasmaphysik, Boltzmannstr. 2, D-85748 Garching (Germany)], E-mail: Kick@arcor.de; Sielanko, Juliusz [Maria Curie Sklodowska University, Pl. M. C. Sklodowskie 1, 20-031 Lublin (Poland); Heinemann, Bernd; Riedl, Rudolf; Speth, Eckehart; Staebler, Albrecht [Max-Planck-Institut fuer Plasmaphysik, Boltzmannstr. 2, D-85748 Garching (Germany)

    2009-06-15

    Neutral Beam Injection (NBI), besides ECRH, is foreseen as one of the main heating devices at the W7-X stellarator currently under construction at IPP Greifswald, Germany. In a final stage 20 MW of NBI heating power will be installed generated by two NBI boxes of the ASDEX Upgrade (AUG) type. Since magnetic fields generally affect the trajectories of charged particles, essentially all the NBI boxes - including ion sources, acceleration sections, neutralisers and deflection magnets - must be shielded against the stray fields of W7-X. In the magnetic stray fields of W7-X there exist significant radial and toroidal components whereas at tokamaks the vertical components are dominant. The power loads on the ion dump and the protecting structures of the deflecting magnets and the beam lines caused by residual beam ions, therefore, will be strongly different. Thus the shielding concept of AUG cannot simply be taken over, but must be carefully redesigned in order to remain below the critical power limits. New modelling calculations of the magnetic shielding, the ion trajectories and the resulting power loads have been carried out for the 'high iota' and 'low shear' experimental scenarios of W7-X. The fields taken for these calculations are modelled by averaging the calculated W7-X stray fields on the one hand, and by fields generated by two-hypothetical-planar coils perpendicular to the x-y plane, on the other hand. The shielding concept for W7-X mainly consist of iron plates in the outer side regions of the boxes and as little magnetic material as possible inside the boxes.

  14. Relationship between the degree of conversion, solubility and salivary sorption of a hybrid and a nanofilled resin composite

    Directory of Open Access Journals (Sweden)

    Eduardo Moreira da Silva

    2008-04-01

    Full Text Available This study analyzed the relationship between the degree of conversion (DC, solubility, and salivary sorption of a hybrid (Filtek P 60 and a nanofilled resin composite (Filtek Supreme, and evaluated the influence of the light-activation mode on these properties. Two light-activation modes were used: Conventional (C; 850 mW/cm² for 20 s and Soft-start (SS; 100-1,000 mW/cm² for 10 s + 1,000 mW/cm² for 10 s. The DC (% was evaluated by FT-Raman spectroscopy. The solubility and salivary sorption were measured after immersion in artificial saliva for 7 days. Data were analyzed by ANOVA and Student-Newman-Keuls' test and linear regression analysis (a = 0.05. The DC varied from 50.52% (nanofilled composite to 57.15% (hybrid composite, and was influenced by the light-activation mode: C > SS. The solubility (0.45 mg/mm³ and salivary sorption (8.04 mg/mm³ of the nanofilled composite were greater than those of the hybrid composite (0.40 mg/mm³ / 6.87 mg/mm³, and were influenced by the light-activation mode: SS > C. Correlation was found between DC and solubility (r = - 0.89, p<0.05, as well as between solubility and salivary sorption (r = 0.95. These findings suggest that nanofilled composites may present higher degradation in the oral environment than hybrid ones. Soft-start light-activation mode may increase the solubility of resin composites.

  15. Constraints on particle acceleration in SS433/W50 from MAGIC and H.E.S.S. observations

    OpenAIRE

    Ahnen, M. L.; Ansoldi, S.; Bednarek, W.; Paiano, S.; Palacio, J.; Paneque, D.; Paoletti, R.; Paredes, J. M.; Paredes-Fortuny, X.; Pedaletti, G.; Peresano, M.; Perri, L.; Persic, M.; Bernardini, E.; Prada Moroni, P. G.

    2018-01-01

    Context. The large jet kinetic power and non-thermal processes occurring in the microquasar SS 433 make this source a good candidate for a very high-energy (VHE) gamma-ray emitter. Gamma-ray fluxes above the sensitivity limits of current Cherenkov telescopes have been predicted for both the central X-ray binary system and the interaction regions of SS 433 jets with the surrounding W50 nebula. Non-thermal emission at lower energies has been previously reported, indicating that efficient partic...

  16. Measurement of the production cross section for W + γ in the electron channel in √s = 1.8 TeV bar pp collisions

    International Nuclear Information System (INIS)

    Benjamin, D.P.

    1993-11-01

    The production cross section times decay branching ratio for W +γ in the electron decay channel in √s = 1.8 TeV bar p-p collisions has been measured using W → eγ data sample obtained from the CDF 1988--1989 Tevatron collider run. For photons in the central region (|η γ | T γ 5.0 GeV and lepton-photon angular separation ΔR ell γ > 0.7, eight electron W γ candidates were observed. From these events, the production cross section times decay branching ratio for the electron sample was measured to be a σ · B(W γ ) exp = 17.0 -13.4 +13.6 (stat. + syst.)pb. The W γ cross section is sensitive to the anomalous couplings of the W boson. Using the W γ cross section measurement, the absence of an excess of large E T photons accompanying the production of a W boson enables one to obtain direct limits on anomalous WW γ couplings. The experimental limits on the anomalous couplings was measured to be -7.2 W ≥ 1 TeV for saturation of unitarity, corresponding to probing a distance scale of order L W ≤ 2.0 x 10 -4 fm. The experimental limits on anomalous WW γ couplings place bounds on the higher-order electromagnetic moments of the W boson -- the magnetic dipole and electric quadrupole moments and the W boson mean-squared charge radius. The experimental results presented in this thesis are in good agreement with Standard Model expectations

  17. Polymerization of dual cure resin cements applied for luting tooth colored fiber posts

    Directory of Open Access Journals (Sweden)

    Ghavam M.

    2007-05-01

    Full Text Available Background and Aim: Insufficient polymerization of resin cements is of considerable clinical importance, because of mechanical deficiencies and biological side effects of uncured resin. Dual cure resin cements are getting popular in luting tooth colored posts and although their curing is claimed to proceed chemically, polymerization efficiency in deep areas of canal is uncertain. The aim of this study was to evaluate degree of polymerization of dual-cure resin cements used for luting translucent and opaque fiber posts in different distances from the light tip. Materials and Methods: In this experimental in vitro study, degree of conversion of two dual cured resin cements, Rely X ARC (3M, ESPE and Nexus 2 (Kerr, USA were measured when used with DT-Light and DT-White posts (RTD, France. The light curing unit used was Optilux 501, with output of 650-700 mw/cm2 with emitting time of 60 seconds. Degree of conversion was measured in three different depths (4, 6, 8 mm by FTIR. The data were analyzed using ANOVA and Post hoc tests. P0.05. Nexus used with DT-Light had lower DC% in 8 mm depth (P<0.05. Nexus used with DT-White showed lower DC% in 8 mm depth compared to 4 mm depth. The control groups of both cements showed significant increased DC% in 4 mm depth compared to 6 and 8 mm depths (P<0.05. DT-White caused decreased DC% in both cements in 4 mm. DT-Light caused increased DC% of Rely X in 6 mm depth compared to DT-White and control. DT-Light increased DC% of Nexus in 6 and 8 mm depths, compared to DT-White and control groups. Conclusion: Based on the results of this study, application of translucent fiber posts has a significant effect on degree of polymerization in dual-cure resin cements, compared to opaque types. Their better light transmission to deep areas due to the effect of optical fibers, can lead to better results.

  18. Ballistic properties of bidirectional fiber/resin composites

    International Nuclear Information System (INIS)

    Dimeski, Dimko; Spaseska, Dijana

    2004-01-01

    The aim of the research was to make evaluation of the ballistic strength of four different fiber/resin composites intended to be used in manufacturing of ballistic items for personal protection. Research has been performed on glass, ballistic nylon, aramid and HPPE (High Performance Polyethylene) plainly woven fabric based composites. As a matrix system, in all cases, polyvinylbutyral modified phenolic resin was used. For the investigation, areal weight range 2 - 9 kg/m 2 chosen was, which is applicable for personal ballistic protection and the ultimate resin content range 20 - 50 vol.%. Ballistic test of the composites has shown that the best results exhibit HPPE based composites; aramid based composites have been the second best followed by the polyamide based composites. The worst results have been shown by the glass based composites. All composites with lower resin content (20%) have performed much better than their counterparts with higher resin content (50 %).The plot of the ballistic strength (V 50 ) versus areal weight has shown a linear increase of V 50 with the increase of areal weight. The ballistic strength of the composites is highly dependant on the fiber/resin ratio and increases with the increase of the fiber content. (Author)

  19. Modelling of Zirconium and Hafnium separation using continuous annular chromatography

    International Nuclear Information System (INIS)

    Moch-Setyadji; Endang Susiantini

    2014-01-01

    Nuclear degrees of zirconium in the form of a metal alloy is the main material for fuel cladding of NPP. Zirconium is also used as sheathing UO 2 kernel in the form of ZrC as a substitute of SiC in the fuel elements of High Temperature Reactor (HTR). Difficulty separating hafnium from zirconium because it has a lot of similarities in the chemical properties of Zr and Hf. Annular chromatography is a device that can be used for separating of zirconium and hafnium to obtain zirconium nuclear grade. Therefore, it is necessary to construct the mathematical modelling that can describe the separation of zirconium and hafnium in the annular chromatography containing anion resin dowex-1X8. The aim of research is to perform separation simulation by using the equilibrium model and mass transfer coefficient resulted from research. Zr and Hf feed used in this research were 26 and 1 g/l, respectively. Height of resin (L), angular velocity (ω) and the superficial flow rate (uz) was varied to determine the effect of each parameter on the separation of Zr and Hf. By using Kd and Dv values resulted previous research. Simulation results showed that zirconium and hafnium can be separated using a continuous annular chromatography with high resin (long bed) 50 cm, superficial flow rate of 0.001 cm/s, the rotation speed of 0.006 rad/min and 20 cm diameter annular. In these conditions the results obtained zirconium concentration of 10,303.226 g/m 3 and hafnium concentration of 12.324 g/m 3 (ppm). (author)

  20. Metal-insulator transition in Si(111)-(4 x 1)/(8 x 2)-In studied by optical spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Speiser, E.; Hinrichs, K.; Cobet, C.; Esser, N. [Leibniz-Institut fuer Analytische Wissenschaften - ISAS - e.V., Albert-Einstein-Str. 9, 12489 Berlin (Germany); Chandola, S. [Leibniz-Institut fuer Analytische Wissenschaften - ISAS - e.V., Albert-Einstein-Str. 9, 12489 Berlin (Germany); School of Physics, Trinity College Dublin 2 (Ireland); Gensch, M. [Helmholtz Zentrum Berlin (Germany); Wippermann, S.; Schmidt, W.G. [Theoretische Physik, Universitaet Paderborn (Germany); Bechstedt, F. [Institut fuer Festkoerpertheorie und -Optik, Friedrich-Schiller-Universitaet, Jena (Germany); Richter, W. [Dipartimento di Fisica, Universita di Roma Tor Vergata, Via della Ricerca Scientifica 1, 00133 Roma (Italy); Fleischer, K.; McGilp, J.F. [School of Physics, Trinity College Dublin 2 (Ireland)

    2010-08-15

    Measurements of the surface vibrational modes and optical response of Si(111)-(4 x 1)/(8 x 2)-In are compiled and a comparison to ab initio calculations performed within DFT-LDA formalism is given. Surface resonant Raman spectroscopy allows identifying a number of surface phonons with high spectral precision. The phase transition of the (4 x 1)-(8 x 2) surface structure is found to be accompanied by characteristic changes of the surface phonons, which are discussed with respect to various structural models suggested. The optical anisotropy of the (8 x 2) phase shows that the anisotropic Drude tail of the (4 x 1) phase is replaced by two peaks at 0.50 and 0.72 eV. The spectroscopic signatures of the (4 x 1) and (8 x 2) phases agree with a metal-insulator transition. The mid-IR-anisotropic optical response of the insulating (8 x 2) phase is interpreted in terms of electronic single particle excitations between surface electronic bands related to the In-nanowire surface. Comparison of the measured optical transitions with DFT ab initio calculations for the hexagon model and the trimer model of the (8 x 2) structure shows evidence for the existence of the hexagon structure. (Abstract Copyright [2010], Wiley Periodicals, Inc.)

  1. Structural and magnetic properties of Mn{sub 50}Fe{sub 50x}Sn{sub x} (x=10, 15 and 20) alloys

    Energy Technology Data Exchange (ETDEWEB)

    Ghosh, Tanmoy [LCMP, S.N. Bose National Centre for Basic Sciences, Kolkata 700106 (India); Agarwal, Sandeep [Haldia Institute of Technology, Haldia 721657 (India); Mukhopadhyay, P.K., E-mail: pkm@bose.res.in [LCMP, S.N. Bose National Centre for Basic Sciences, Kolkata 700106 (India)

    2016-11-15

    In this work we report measurements and comparisons of the structural, magnetic and transport properties of a series of Mn{sub 50}Fe{sub 50x}Sn{sub x} alloys (x=10, 15 and 20). We found that while the lower Sn composition sample stabilized in β-Mn-type crystallographic phase, the higher Sn composition alloys contained both β-Mn-type as well as Mn{sub 3}Sn-type hexagonal DO{sub 19} phases. Through d.c. and a.c. magnetic property measurements we have established the existence of a ferromagnetic transition near room temperature followed by a spin reorientation at lower temperature in the Mn{sub 3}Sn-type crystallographic phase of the alloys. Our resistivity study also revealed an interesting behavior with negative temperature coefficient (TCR) in these alloys. - Highlights: • Mn{sub 50}Fe{sub 50-x}Sn{sub x} alloys were studied over a limited concentration range. • Lower Sn alloys behaved similar to ß-Mn alloys both structurally and magnetically. • Higher Sn alloys showed magnetic transitions similar to Mn{sub 3}Sn and Fe{sub 3}Sn. • Resistivity showed bad metallic behavior with negetive temperature coefficient.

  2. Efficiencies and Optimization of Weak Base Anion Ion-Exchange Resin for Groundwater Hexavalent Chromium Removal at Hanford

    International Nuclear Information System (INIS)

    Nesham, Dean O.; Ivarson, Kristine A.; Hanson, James P.; Miller, Charles W.; Meyers, P.; Jaschke, Naomi M.

    2014-01-01

    The U.S. Department of Energy's (DOE's) contractor, CH2M HILL Plateau Remediation Company, has successfully converted a series of groundwater treatment facilities to use a new treatment resin that is delivering more than $3 million in annual cost savings and efficiency in treating groundwater contamination at the DOE Hanford Site in southeastern Washington State. During the production era, the nuclear reactors at the Hanford Site required a continuous supply of high-quality cooling water during operations. Cooling water consumption ranged from about 151,417 to 378,541 L/min (40,000 to 100,000 gal/min) per reactor, depending on specific operating conditions. Water from the Columbia River was filtered and treated chemically prior to use as cooling water, including the addition of sodium dichromate as a corrosion inhibitor. Hexavalent chromium was the primary component of the sodium dichromate and was introduced into the groundwater at the Hanford Site as a result of planned and unplanned discharges from the reactors starting in 1944. Groundwater contamination by hexavalent chromium and other contaminants related to nuclear reactor operations resulted in the need for groundwater remedial actions within the Hanford Site reactor areas. Beginning in 1995, groundwater treatment methods were evaluated, leading to the use of pump-and-treat facilities with ion exchange using Dowex 21K, a regenerable, strong-base anion exchange resin. This required regeneration of the resin, which was performed offsite. In 2008, DOE recognized that regulatory agreements would require significant expansion for the groundwater chromium treatment capacity. As a result, CH2M HILL performed testing at the Hanford Site in 2009 and 2010 to demonstrate resin performance in the specific groundwater chemistry at different waste sites. The testing demonstrated that a weak-base anion, single-use resin, specifically ResinTech SIR-700 ®, was effective at removing chromium, had a significantly higher

  3. Characteristic 8 keV X rays possess radiobiological properties of higher-LET radiation.

    Science.gov (United States)

    Shridhar, Ravi; Estabrook, William; Yudelev, Mark; Rakowski, Joseph; Burmeister, Jay; Wilson, George D; Joiner, Michael C

    2010-03-01

    Electronic brachytherapy systems are being developed that can deliver X rays of varying energy depending on the material of a secondary target. A copper target produces characteristic 8 keV X rays. Our aim was to determine whether 8 keV X rays might deliver greater biological effectiveness than megavoltage photons. Cells of the U251 human glioma cell line were used to compare the biological effects of 8 keV X rays and (60)Co gamma rays in terms of relative biological effectiveness (RBE), oxygen enhancement ratio (OER), and DNA damage. The RBE at 50% and 10% survival was 2.6 and 1.9, respectively. At 50% survival, the OER for cells treated with 8 keV X rays was 1.6 compared with 3.0 for (60)Co gamma rays. The numbers of H2AX foci per Gy after treatment with 8 keV X rays and (60)Co gamma rays were similar; however, the size of the foci generated at 8 keV was significantly larger, possibly indicating more complex DNA damage. The mean area of H2AX foci generated by 8 keV X rays was 0.785 microm(2) (95% CI: 0.756-0.814) compared with 0.491 microm(2) (95% CI: 0.462-0.520) for (60)Co gamma rays (P X rays produce two to three times the biological effectiveness of megavoltage photons, with a radiobiological profile similar to higher-LET radiations.

  4. {8-14C}-Adenine and {1-14C}-isopentenyl pyrophosphate - precursors for root-produced cytokinins in the tomato (Lycopersicon esculentum mill.)

    International Nuclear Information System (INIS)

    Dickinson, J.R.

    1985-01-01

    Following the detection of reasonable levels of biologically active cytokinin-like compounds in one-month-old tomato plants, the possible involvement of {8- 14 C}-adenine and {1- 14 C}-isopentenyl pyrophosphate in the biosynthetic pathway leading to an accumulation of free zeatin derivatives, was studied. Intact tomato plants were used for a time-course study involving the uptake of {8- 14 C}-adenine and the tentative identification of compounds into which the 14 C became incorporated. Using high performance liquid chromatography, radioactive trans-zeatin was identified as being present in the Dowex 50 root extract. The 12-hour time interval was used and the roots of the tomato plants were immersed in a more heavily radiolabelled medium. Modified separation techniques were used to achieve enhanced radioactivity recovery rates. This experiment demonstrated the presence of relatively high levels of tentatively identified radioactive zeatin in the Dowex 50 root and stem extracts. Radioactivity in the aqueous extracts was found not to be contributed by cytokinin nucleotides. A final experiment was carried out using decapitated root systems to determine if the root tissue alone could be implicated in the synthesis of cytokinins. Decapitated tomato root systems were supplied with either {8- 14 C}-adenine or {1- 14 C}-isopentenyl pyrophosphate. The ratio of incorporation of {1- 14 C}-isopentenyl pyrophosphate into identified cytokinins was higher than for {8- 14 C}-adenine. It was concluded that both adenine and isopentenyl pyrophosphate are involved in the biosynthetic pathway leading to an accumulation of free zeatin derivatives in tomato roots

  5. Borehole data package for wells 299-W22-48, 299-W22-49, and 299-W22-50 at single-shell tank waste management Area S-SX

    International Nuclear Information System (INIS)

    Horton, D.G.; Johnson, V.G.

    2000-01-01

    Three new Resource Conservation and Recovery Act (RCRA) groundwater monitoring wells were installed at the single-shell tank farm Waste Management Area (WMA) S-SX in October 1999 through February 2000 in fulfillment of Tri-Party Agreement (Ecology 1996) milestone M-24-41. The wells are 299-W22-48, 299-W22-49, and 299-W22-50. Well 299-W22-48 is located east of the southeast corner of 241-S tank farm and is a new downgradient well in the monitoring network. Well 299-W22-49 is located on the east side of the 241-SX tank farm, adjacent to well 299-W22-39, which it replaces in the monitoring network. Well 299-W22-50 is located at the southeast corner of the 241-SX tank farm and is a replacement for downgradient monitoring well 299-W22-46, which is going dry. The original assessment monitoring plan for WMA S-SX was issued in 1996 (Caggiano 1996). That plan was updated for the continued assessment at WMA S-SX in 1999 (Johnson and Chou 1999). The updated plan provides justification for the new wells. The new wells were constructed to the specifications and requirements described in Washington Administrative Code (WAC) 173-160 and WAC 173-303, the updated assessment plan for WMA S-SX (Johnson and Chou 1999), and the description of work for well drilling and construction. This document compiles information on the drilling and construction, well development, pump installation, and sediment and groundwater sampling applicable to the installation of wells 299-W22-48, 299-W22-49 and 299-W22-50. Appendix A contains the Well Summary Sheets (as-built diagrams), the Well Construction Summary Reports, and the geologist's logs. Appendix B contains results of laboratory analyses of the physical properties of sediment samples obtained during drilling. Appendix C contains borehole geophysical logs, and Appendix D contains the analytical results from groundwater samples obtained during well drilling and construction

  6. Borehole data package for wells 299-W22-48, 299-W22-49, and 299-W22-50 at single-shell tank waste management Area S-SX

    Energy Technology Data Exchange (ETDEWEB)

    DG Horton; VG Johnson

    2000-05-18

    Three new Resource Conservation and Recovery Act (RCRA) groundwater monitoring wells were installed at the single-shell tank farm Waste Management Area (WMA) S-SX in October 1999 through February 2000 in fulfillment of Tri-Party Agreement (Ecology 1996) milestone M-24-41. The wells are 299-W22-48, 299-W22-49, and 299-W22-50. Well 299-W22-48 is located east of the southeast corner of 241-S tank farm and is a new downgradient well in the monitoring network. Well 299-W22-49 is located on the east side of the 241-SX tank farm, adjacent to well 299-W22-39, which it replaces in the monitoring network. Well 299-W22-50 is located at the southeast corner of the 241-SX tank farm and is a replacement for downgradient monitoring well 299-W22-46, which is going dry. The original assessment monitoring plan for WMA S-SX was issued in 1996 (Caggiano 1996). That plan was updated for the continued assessment at WMA S-SX in 1999 (Johnson and Chou 1999). The updated plan provides justification for the new wells. The new wells were constructed to the specifications and requirements described in Washington Administrative Code (WAC) 173-160 and WAC 173-303, the updated assessment plan for WMA S-SX (Johnson and Chou 1999), and the description of work for well drilling and construction. This document compiles information on the drilling and construction, well development, pump installation, and sediment and groundwater sampling applicable to the installation of wells 299-W22-48, 299-W22-49 and 299-W22-50. Appendix A contains the Well Summary Sheets (as-built diagrams), the Well Construction Summary Reports, and the geologist's logs. Appendix B contains results of laboratory analyses of the physical properties of sediment samples obtained during drilling. Appendix C contains borehole geophysical logs, and Appendix D contains the analytical results from groundwater samples obtained during well drilling and construction.

  7. Effect of the molecular structure of phenolic novolac precursor resins on the properties of phenolic fibers

    International Nuclear Information System (INIS)

    Ying, Yong-Gang; Pan, Yan-Ping; Ren, Rui; Dang, Jiang-Min; Liu, Chun-Ling

    2013-01-01

    A series of phenolic resins with different weight-average molecular weights (M w ) and ortho/para (O/P) ratios were prepared. The effect of the phenolic precursor resin structure on the structure and properties of the resulting phenolic fibers was investigated. The structures of the resins and fibers were characterized by nuclear magnetic resonance spectroscopy, gel permeation chromatography, melt rheometry, dynamic mechanical analysis, and thermogravimetric analysis. The results show that the O/P ratio, unsubstituted ortho and para carbon ratio (O u /P u ), and M w of the phenolic resins play an important role in determining the properties of the phenolic fibers. The tensile strength of the phenolic fibers increases with increasing novolac precursor O u /P u ratios, corresponding to low O/P ratios, at comparable resin M w values. Also, the tensile strength of the phenolic fibers increases with increasing novolac M w values at comparable O/P ratios. Phenolic fibers with high tensile strength and good flame resistance characteristics were generated from a phenolic precursor resin, possessing a high weight-average molecular weight and a low O/P value. - Highlights: • Phenolic resins with different weight-average molecular weights and ortho/para ratios have been prepared. • The tensile strength of the phenolic fibers increases with reducing novolac O/P ratio. • The tensile strength of the phenolic fibers increases with increasing novolac M w

  8. Novel red phosphors KBaEu(XO4)3 (X = Mo, W) show high color purity and high thermostability from a disordered chained structure.

    Science.gov (United States)

    Wang, G Q; Gong, X H; Chen, Y J; Huang, J H; Lin, Y F; Luo, Z D; Huang, Y D

    2017-05-23

    Two novel red phosphors KBaEu(XO 4 ) 3 (X = Mo, W) have been synthesized by high-temperature solid-state reactions and the crystal structures were determined for the first time. Single-crystal X-ray diffraction data reveal that their space groups are C2/c. The crystalline structure is constituted of K/BaO 8 distorted square antiprisms and distorted EuO 8 polyhedra which form chains lying along the c-axis and two kinds of distorted XO 4 tetrahedra. This high disorder of K/Ba which might lower the crystal field symmetry around Eu 3+ results in the high purity of red emission around 615 nm originating from 5 D 0 → 7 F 2 transition under near-ultraviolet (NUV) excitation. With increasing temperature, the luminescence of KBaEu(XO 4 ) 3 (X = Mo, W) phosphors decreases almost linearly with subtle alteration for the CIE coordinate. As the temperature reaches 550 K, the red emission intensity decreases to 37.3% and 50.7% of that at 300 K for KBaEu(MoO 4 ) 3 and KBaEu(WO 4 ) 3 , respectively. The analysis of the decay curves of the 5 D 0 → 7 F 2 emission at variable temperatures indicates the weak cross relaxation and non-radiative energy transfer between Eu 3+ ions. These results demonstrate that the investigated phosphors are attractive for application in high power NUV excited white LEDs.

  9. Mechanical properties of dental resin composites by co-filling diatomite and nanosized silica particles

    International Nuclear Information System (INIS)

    Wang Hua; Zhu Meifang; Li Yaogang; Zhang Qinghong; Wang Hongzhi

    2011-01-01

    The aim of this study was to investigate the mechanical property effects of co-filling dental resin composites with porous diatomite and nanosized silica particles (OX-50). The purification of raw diatomite by acid-leaching was conducted in a hot 5 M HCl solution at 80 deg. C for 12 h. Both diatomite and nanosized SiO 2 were silanized with 3-methacryloxypropyltrimethoxysilane. The silanized inorganic particles were mixed into a dimethacrylate resin. Purified diatomite was characterized by X-ray diffraction, UV-vis diffuse reflectance spectroscopy and an N 2 adsorption-desorption isotherm. Silanized inorganic particles were characterized using Fourier transform infrared spectroscopy and a thermogravimetric analysis. The mechanical properties of the composites were tested by three-point bending, compression and Vicker's microhardness. Scanning electron microscopy was used to show the cross-section morphologies of the composites. Silanization of diatomite and nanosized silica positively reinforced interactions between the resin matrix and the inorganic particles. The mechanical properties of the resin composites gradually increased with the addition of modified diatomite (m-diatomite). The fracture surfaces of the composites exhibited large fracture steps with the addition of m-diatomite. However, when the mass fraction of m-diatomite was greater than 21 wt.% with respect to modified nanosized silica (mOX-50) and constituted 70% of the resin composite by weight, the mechanical properties of the resin composites started to decline. Thus, the porous structure of diatomite appears to be a crucial factor to improve mechanical properties of resin composites.

  10. Influence of surface conditions and silane agent on the bond of resin to IPS Empress 2 ceramic.

    Science.gov (United States)

    Spohr, Ana Maria; Sobrinho, Lourenço Correr; Consani, Simonides; Sinhoreti, Mario Alexandre Coelho; Knowles, Jonathan C

    2003-01-01

    The aim of this study was to evaluate the effect of different ceramic surface treatments on the tensile bond strength between IPS Empress 2 ceramic framework and Rely X adhesive resin cement, with or without the application of a silane coupling agent. One hundred twenty disks were made, embedded in resin, and randomly divided into six groups: group 1 = sandblasting (100 microm), no silanation; group 2 = sandblasting (100 microm), silane treatment; group 3 = sandblasting (50 microm), no silanation; group 4 = sandblasting (50 microm), silane treatment; group 5 = hydrofluoric acid etching, no silanation; and group 6 = hydrofluoric acid etching, silane treatment. The disks were bonded into pairs with adhesive resin cement. All samples were stored in distilled water at 37 degrees C for 24 hours and then thermocycled. The samples were submitted to tensile testing. The use of silane improved the bond strength in relation to the groups in which silane was not applied (P Empress 2 ceramic framework and resin agent.

  11. Ultra-short-period W/B4C multilayers for x-ray optics-microstructure limits on reflectivity

    Energy Technology Data Exchange (ETDEWEB)

    Walton, Christopher Charles [Univ. of California, Berkeley, CA (United States). Dept. of Materials Science and Mineral Engineering

    1997-12-01

    Multilayer thin films are used as Bragg reflectors for soft x-rays in the energy range 50eV < E < 1000eV in many x-ray optics applications such as x-ray microscopes and telescopes, reducing optics for extreme ultraviolet (EUV) lithography, and x-ray polarizers and phase retarders. Applications often depend critically on reflectivity, which has not been systematically characterized for multilayer periods below 20Å. For this study, W/B4C multilayers were fabricated by magnetron sputtering on Si(111), with periods from 48Å to as little as 4.7Å. The x-ray reflectivity measured at λ = 1.54Å and at 45° incidence (289 eV < E < 860 eV) was found to decrease sharply for multilayer periods less than 15-20Å. Examination by high-resolution transmission electron microscopy (HRTEM) showed an expansion of the thickness of the W-rich layers of 30-40% from the nominal values, consistent with intermixture of the two materials during sputter growth, and discontinuous W-rich layers for multilayer periods below about 15Å. The experimental data for the specular reflectivity in the hard and soft x-ray regimes and the diffuse scattering fit well to a model of multilayer roughness. The model is expressed as a power-law dependence of roughness on spatial frequency. Analysis of small-angle scattering in transmission from multilayers grown on freestanding Si3N4 membranes confirms the onset of discontinuity at periods between 14Å and 22Å. Spectroscopy studies by x-ray absorption (NEXAFS) and electron energy loss (EELS) at the boron K-edge (188eV) are consistent with changes in the average boron bonding environment, as the multilayer period decreases and the W-rich layers are increasingly thin and dispersed. A discrete W-rich phase is present for periods at least as small as 6.3Å.

  12. Electrochemical behavior of Ni{sub x}W{sub 1-x} materials as catalyst for hydrogen evolution reaction in alkaline media

    Energy Technology Data Exchange (ETDEWEB)

    Oliver-Tolentino, Miguel A. [UPIBI-IPN, Departamento de Ciencias Basicas, Av. Acueducto s/n, Barrio La Laguna, Col. Ticoman, Mexico D.F. 07340 (Mexico); Arce-Estrada, Elsa M. [ESIQIE-IPN Departamento de Ingenieria en Metalurgia y Materiales, UPALM, UPALM, Mexico D.F. 07738 (Mexico); Cortes-Escobedo, Claudia A. [Centro de Investigacion e Innovacion Tecnologica del IPN, Cda. Cecati s/n, Col. Sta. Catarina, CP 02250 Azcapotzalco D.F. (Mexico); Bolarin-Miro, Ana M.; Sanchez-De Jesus, Felix [Area Academica de Ciencias de la Tierra y Materiales, Universidad Autonoma del Estado de Hidalgo, CU, Carr. Pachuca-Tulancingo Km. 4.5, Mineral de la Reforma, CP 42184 Hidalgo (Mexico); Gonzalez-Huerta, Rosa de G. [ESIQIE-IPN, Departamento de Ingenieria Quimica - Laboratorio de Electroquimica y Corrosion, Edif. Z-5 3er piso, UPALM, Mexico D.F. 07738 (Mexico); Manzo-Robledo, Arturo, E-mail: amanzor@ipn.mx [ESIQIE-IPN, Departamento de Ingenieria Quimica - Laboratorio de Electroquimica y Corrosion, Edif. Z-5 3er piso, UPALM, Mexico D.F. 07738 (Mexico)

    2012-09-25

    Highlights: Black-Right-Pointing-Pointer The electrochemical techniques used in this study elucidated the Ni-W surface state. Black-Right-Pointing-Pointer The Ni-W materials were effective for the hydrogen evolution reaction. Black-Right-Pointing-Pointer The prepared alloys exhibited higher catalytic activity than their precursors. Black-Right-Pointing-Pointer The preparation method is relatively simple and effective procedure. - Abstract: In the present work, results of electrochemical evaluation, as well as morphological and structural characterization of Ni{sub x}W{sub 1-x} materials with x = 0.77, 0.64, 0.4, 0.19 and 0.07 processed by means of high energy ball milling from high purity powders are presented. Also, the electrocatalytic performance on the hydrogen evolution reaction (HER) of the Ni{sub x}W{sub 1-x} materials evaluated by linear polarization and cyclic voltammetry techniques in alkaline media at room temperature is discussed. The structural and morphological characterization of the as-prepared materials was carried out using X-ray diffraction (XRD) and scanning electron microscopy (SEM). Results indicated a small-particle clusters and solid solution formation. According to the kinetics parameters the best electrocatalytic activity was observed at Ni{sub 64}W{sub 36}.

  13. Change of manufacturing technique for the W7-X nonplanar coil cases

    International Nuclear Information System (INIS)

    Gehring, M.; Schaefer, P.; Herrmann, K.D.; Scheller, H.

    2001-01-01

    The geometry of the coil cases of the nonplanar coil system for the Wendelstein 7-X (W7-X) experiment (Sapper, The superconducting magnet system for the W7-X stellarator. Proceedings 12th Topical Meeting on the Fusion Technology) was changed to a more complex shape compared to the DEMO Coil case (Kronhardt et al., 1998. Proceedings of the 20th SOFT (1998) 731-734). Therefore the manufacturing technique developed for the DEMO Coil case cannot be used for the series production of 50 coils. For the final design of the coil cases, investigations were performed to find a technique suitable for manufacturing the cases within the required geometrical tolerances and mechanical characteristics. In order to qualify the manufacturing technique a complete half case was cast and machined afterwards. The casting procedure was optimised with respect to the geometrical accuracy and the mechanical characteristics at 4.2 K. Measurements of the yield strength, the tensile strength, the elongation, and the Young's modulus were performed at room- and cryo-temperature (4 and 7 K). The influence of the heat treatment, the annealing temperature and the size of the casting on the mechanical values is shown. The requirements on the stainless steel are a yield strength of 800 MPa at 4 K and an elongation at fracture of >25%. The magnetic permeability has to be <1.01. Furthermore the welding properties of the case material were investigated. The development program showed that casting of complete case half shells is a feasible manufacturing technique for the series production of the Wendelstein 7-X nonplanar coil cases

  14. INTEGRAL finds renewed X-ray activity of the Neutron star X-ray transient SAX J1750.8-2900

    DEFF Research Database (Denmark)

    Sanchez-Fernandez, Celia; Chenevez, Jérôme; Kuulkers, Erik

    2015-01-01

    INTEGRAL Galactic bulge monitoring observations (ATel #438) on UT 13 September 2015 18:50-22:32 reveal renewed X-ray activity from the low-mass X-ray binary transient and Type I X-ray burster SAX J1750.8-2900 (IAU Circ. #6597). The last outburst from this source was reported in 2011 (ATels #3170,...

  15. Interacting large-scale magnetic fields and ionized gas in the W50/SS433 system

    Science.gov (United States)

    Farnes, J. S.; Gaensler, B. M.; Purcell, C.; Sun, X. H.; Haverkorn, M.; Lenc, E.; O'Sullivan, S. P.; Akahori, T.

    2017-06-01

    The W50/SS433 system is an unusual Galactic outflow-driven object of debatable origin. We have used the Australia Telescope Compact Array to observe a new 198 pointing mosaic, covering 3° × 2°, and present the highest-sensitivity full-Stokes data of W50 to date using wide-field, wide-band imaging over a 2 GHz bandwidth centred at 2.1 GHz. We also present a complementary Hα mosaic created using the Isaac Newton Telescope Photometric Hα Survey of the Northern Galactic Plane. The magnetic structure of W50 is consistent with the prevailing hypothesis that the nebula is a reanimated shell-like supernova remnant (SNR), which has been re-energized by the jets from SS433. We observe strong depolarization effects that correlate with diffuse Hα emission, likely due to spatially varying Faraday rotation measure (RM) fluctuations of ≥48-61 rad m-2 on scales ≤4.5-6 pc. We also report the discovery of numerous, faint, Hα filaments that are unambiguously associated with the central region of W50. These thin filaments are suggestive of an SNR's shock emission, and almost all have a radio counterpart. Furthermore, an RM-gradient is detected across the central region of W50, which we interpret as a loop magnetic field with a symmetry axis offset by ≈90° to the east-west jet-alignment axis, and implying that the evolutionary processes of both the jets and the SNR must be coupled. A separate RM-gradient is associated with the termination shock in the eastern ear, which we interpret as a ring-like field located where the shock of the jet interacts with the circumstellar medium. Future optical observations will be able to use the new Hα filaments to probe the kinematics of the shell of W50, potentially allowing for a definitive experiment on W50's formation history.

  16. Determination of uranium in urine by 2-spectrometry

    International Nuclear Information System (INIS)

    Duarte, C.L.; Szeles, M.S.-M.F.

    1989-07-01

    A comparative study is presented for two technics of preparation sources for the determination of uranium isotopes by α - spectrometry: electrodeposition and chemical stripping with polymeric membrane containing trioctylphosphine oxide (TOPO). A method is described for separation of uranium from urine with an ion-exchange column Dowex 1x8 (chloride form). The mean yield obtained for electrodeposition and TOPO deposition was 74% and 8,5% respectively. The TOPO deposition presented better resolution for 238 U and 234 U than electrodeposition. The global yield of the method obtained was 50%. (author) [pt

  17. Reducing elution in anion exchange chromatography as a pretreatment of colorimetry of chromium(VI) and vanadium(V)

    International Nuclear Information System (INIS)

    Shigetomi, Yasumasa; Hatamoto, Takeji; Nagoshi, Kimie; Yamashige, Takashi.

    1976-01-01

    In order to increase the selectivity of the colorimetry of chromium and vanadium, the separation by means of anion exchange chromatography was tested. The column, phi 0.8x5.0 cm packing (50--100 mesh) Dowex 1x4 anion exchange resin was used for the separation of chromium. The solution containing chromium (VI), zinc(II), cadmium(II), iron(III) and reducing organic substances contained in industrial waste water was introduced into the column and then the substances other than chromium(VI) were removed by washing the column with distilled water. Finally chromium(VI) was reduced to chromium(III) by hydroxylamine in the eluent and eluted. The concentration of sulfuric acid and hydroxylamine in the eluent were 0.1 mol/l and 0.001 mol/l respectively. For analyzing chromium(III) in the mixture of chromium(VI) and chromium(III), after removal of chromium(VI) it should be oxidized to chromium(VI) anion with the oxidant, e.g., sodium peroxide or hydrogen peroxide, before introducing it into the column. In terms of the pretreatment by using the acetate form resin column, chromium (VI) and chromium(III) can be determined separately in the solution whose concentration ranges from 0.05 ppm to 0.5 ppm despite the presence of contaminants, which interfere with the colorimetric determination of chromium(VI) using diphenylcarbonohydrazide, in the original solution. The separation of vanadium(V) in the solution containing copper(II), cobalt(II) and etc. was made using the mixed solution of hydrochloric acid (2 mol/l) and hydroxylamine (0.2 mol/l) similarly to chromium(VI). In terms of the similar pretreatment vanadium could be determined precisely as far as 0.1 ppm by the colorimetry using 4-(2-pyridylazo) resorcinol despite the presence of copper(II), cobalt(II), nickel(II) and etc in the original solution. (auth.)

  18. Synthesis and Characterization of 8-Yttrium(III-Containing 81-Tungsto-8-Arsenate(III, [Y8(CH3COO(H2O18(As2W19O684(W2O62(WO4]43−

    Directory of Open Access Journals (Sweden)

    Masooma Ibrahim

    2015-06-01

    Full Text Available The 8-yttrium(III-containing 81-tungsto-8-arsenate(III [Y8(CH3COO(H2O18(As2W19O684(W2O62(WO4]43− (1 has been synthesized in a one-pot reaction of yttrium(III ions with [B-α-AsW9O33]9− in 1 M NaOAc/HOAc buffer at pH 4.8. Polyanion 1 is composed of four {As2W19O68} units, two {W2O10} fragments, one {WO6} group, and eight YIII ions. The hydrated cesium-sodium salt of 1 (CsNa-1 was characterized in the solid-state by single-crystal XRD, FT-IR spectroscopy, thermogravimetric and elemental analyses.

  19. Development of radiochemical separation method for determination of toxic elements in biological samples

    International Nuclear Information System (INIS)

    Maihara, V.A.; Vasconcellos, M.B.A.; Favaro, D.I.T.; Armelin, M.J.A.

    1990-01-01

    In order to determine Hg, Sb, As and Se in biological materials by neutron activation analysis, a radiochemical separation was developed. The chemical separation procedure used was based on the digestion of the irradiated sample in a mixture of H NO 3 and H 2 SO 4 in a teflon bomb, at 130 0 C for 1 to 4 hours. After the dissolution of organic matter, Hg and Sb were retained by a Dowex 2-X8 resin column in 6 M HCl. The effluent was passed through a TDO, tin dioxide column which retains As and Se in 3 M HCl medium. Radioactive tracers of these elements were used to determine the yields of the separation process. Certified reference materials were analyzed to check the precision and accuracy of the method. (author)

  20. Comparison of temperature change among different adhesive resin cement during polymerization process

    Directory of Open Access Journals (Sweden)

    Murat Alkurt

    2017-01-01

    Full Text Available Purpose: The aim of this study was to assess the intra-pulpal temperature changes in adhesive resin cements during polymerization. Materials and Methods: Dentin surface was prepared with extracted human mandibular third molars. Adhesive resin cements (Panavia F 2.0, Panavia SA, and RelyX U200 were applied to the dentin surface and polymerized under IPS e.max Press restoration. K-type thermocouple wire was positioned in the pulpal chamber to measure temperature change (n = 7. The temperature data were recorded (0.0001 sensible and stored on a computer every 0.1 second for sixteen minutes. Differences between the baseline temperature and temperatures of various time points (2, 4, 6, 8, 10, 12, 14, and 16 minute were determined and mean temperature changes were calculated. At various time intervals, the differences in temperature values among the adhesive resin cements were analyzed by two-way ANOVA and post-hoc Tukey honestly test (α = 0.05. Results: Significant differences were found among the time points and resin cements (P < 0.05. Temperature values of the Pan SA group were significantly higher than Pan F and RelyX (P < 0.05. Conclusion: Result of the study on self-adhesive and self-etch adhesive resin cements exhibited a safety intra-pulpal temperature change.

  1. Urea-formaldehyde resins: production, application, and testing

    Science.gov (United States)

    Nuryawan, A.; Risnasari, I.; Sucipto, T.; Heri Iswanto, A.; Rosmala Dewi, R.

    2017-07-01

    Urea-formaldehyde (UF) resin, one of the most important formaldehyde resin adhesives, is a polymeric condensation product of formaldehyde with urea, and being widely used for the manufacture of wood-based composite panels, such as plywood, particleboard, and fiberboard. In spite of its benefits such as fast curing, good performance in the panels (colorless), and lower cost; formaldehyde emission (FE) originated from either UF resin itself or composite products bonded by UF resins is considered a critical drawback as it affects human health particularly in indoor environment. In order to reduce the FE, lowering formaldehyde/urea (F/U) mole ratio in the synthesis of the UF resin was done. In this study, synthesis of UF resins was carried out following the conventional alkaline-acid two-step reaction with a second addition of urea, resulting in F/U mole ratio around 1.0, namely 0.95; 1.05, and 1.15. The UF resins produced were used as binder for particleboard making. The board was manufactured in the laboratory using shaving type particle of Gmelina wood, 8% UF resin based on oven dry particle, and 1% NH4Cl (20%wt) as hardener for the resin. The target of the thickness was 10 mm and the dimension was 25 cm x 25 cm. The resulted particleboard then was evaluated the physical and the mechanical properties by Japanese Industrial Standard (JIS) A 5908 (2003). Further, the resulted particleboard also was used for the mice cage’s wall in order to mimic the real living environment. After four weeks exposure in the cages, the mice then were evaluated their mucous organs as well as their blood. The experiment results were as follows: 1) It was possible to synthesis UF resins with low F/U mole ratio; 2) However, the particleboard bonded UF resins with low F/U mole ratio showed poor properties, particularly on the thickness swelling and modulus of elasticity; 3) There was no significant differences among the mucous organs of the mice after a month exposure FE originated from

  2. Adhesive bonding of resin composite to various titanium surfaces using different metal conditioners and a surface modification system

    Directory of Open Access Journals (Sweden)

    Hercules Jorge ALMILHATTI

    2013-12-01

    Full Text Available Objective: This study evaluated the effect of three metal conditioners on the shear bond strength (SBS of a prosthetic composite material to cpTi grade I having three surface treatments. Material and Methods: One hundred sixty eight rivet-shaped specimens (8.0x2.0 mm were cast and subjected to polishing (P or sandblasting with either 50 mm (50SB or 250 mm (250SB Al2O3. The metal conditioners Metal Photo Primer (MPP, Cesead II Opaque Primer (OP, Targis Link (TL, and one surface modification system Siloc (S, were applied to the specimen surfaces, which were covered with four 1-mm thick layers of resin composite. The resin layers were exposed to curing light for 90 s separately. Seven specimens from each experimental group were stored in water at 37ºC for 24 h while the other 7 specimens were subjected to 5,000 thermal cycles consisting of water baths at 4ºC and 60ºC (n=7. All specimens were subjected to SBS test (0.5 mm/min until failure occurred, and further 28 specimens were analyzed using scanning electron microscope (SEM and X-ray energy-dispersive spectroscopy (EDS. Data were analyzed by 3-way ANOVA followed by post-hoc Tukey's test (α=0.05. Results: On 50SB surfaces, OP groups showed higher SBS means than MPP (P<0.05, while no significant difference was found among OP, S, and TL groups. On 250SB surfaces, OP and TL groups exhibited higher SBS than MPP and S (P<0.05. No significant difference in SBS was found between OP and TL groups nor between MPP and S groups. The use of conditioners on 250SB surfaces resulted in higher SBS means than the use of the same products on 50SB surfaces (P<0.05. Conclusion: Sandblasting associated with the use of metal conditioners improves SBS of resin composites to cpTi.

  3. Effect of cavity preparation on the flexural strengths of acrylic resin repairs

    Science.gov (United States)

    ELHADIRY, Safa Salim; YUNUS, Norsiah; ARIFFIN, Yusnidar Tajul

    2010-01-01

    Objective To investigate the effect of cavity preparation on the flexural strength of heat-curing denture resin when repaired with an auto-curing resin. Material and methods Ninety-six rectangular specimens (64x10x2.5 mm) prepared from heat-curing denture base resin (Meliodent) were randomly divided into four groups before repair. One group was left intact as control. Each repair specimen was sectioned into two; one group was repaired using the conventional repair method (Group 1). Two groups had an additional transverse cavity (2x3.5x21.5 mm) prepared prior to the repair; one repaired with (Group 2) and one without glass-fiber reinforcement (Group 3). A three-point flexural bending test according to the ISO 1567:1999 specification8 for denture base polymers was carried out on all groups after 1, 7 and 30 days of water immersion. Statistical analysis was carried out using two-way ANOVA, Kruskal Wallis and post-hoc Mann Whitney tests. Results The highest flexural strength was observed in the control group. Control and conventional repairs group (Group 1) showed reduction in the flexural strength 30 days after water immersion. No significant change in the strength was observed for Groups 2 and 3 where the repair joints were similarly prepared with additional transverse cavity. Conclusion Repaired specimens showed lower flexural strength values than intact heat-curing resin. Cavity preparation had no significant effect on the flexural strength of repair with water immersion. PMID:21308283

  4. Blade-type X-ray beam position monitors for SPring-8 undulator beamlines

    CERN Document Server

    Aoyagi, H; Kitamura, H

    2001-01-01

    The X-ray beam position monitors had been designed and installed for SPring-8 insertion device beamlines. These monitors are being utilized for photon beam diagnostics. The beam from the standard undulator in SPring-8 has the total power of 11 kW and the power density of 470 kW/mrad sup 2 , typically. Each monitor has four CVD diamond blades coated with metal for detector heads. We have already introduced three styles of monitors to match various insertion devices in SPring-8. A standard style, or a fixed-blade style, is used mainly for a standard in-vacuum undulator beamlines. A horizontal-blade-drive style and a four-blade-drive style are used for beamlines of a wiggler and a twin helical undulator that have wide power distributions, and for figure-8 undulators that have asymmetric power distributions, respectively. This report describes the design and the structure of these monitors and the beam-tests for the photon beam diagnostics in detail.

  5. Experience with High Voltage Tests of the W7-X Magnets in Paschen-Minimum Conditions

    International Nuclear Information System (INIS)

    Petersen-Zarling, B.M.; Risse, K.; Viebke, H.; Gustke, D.; Ehmler, H.; Baldzuhn, J.; Sborchia, C.; Scheller, H.

    2006-01-01

    The W7-X machine is a low-shear stellarator of the Wendelstein line, which is being assembled at the IPP Branch Institute of Greifswald, Germany. The machine features a superconducting magnet system with 50 non-planar and 20 planar magnets operated at about 6 T and discharged with peak voltage levels up to 6 kV. Following the factory tests, the magnets are delivered to CEA Saclay, France, for the final acceptance tests at cryogenic condition. A series of high voltage tests in air and vacuum are part of the final acceptance test. During these tests the quality of the insulation, especially the hand-wrapped ground insulation in the termination area, has proven not to be adequate. In order to improve the reliability of the insulation system and detect defects for early repair, high voltage tests in reduced pressure of air (Paschen-minimum conditions) have been added as part of the factory acceptance procedure. This has been implemented in the vacuum chambers of BNN/Ansaldo for the test of the 50 non-planar coils, while other tests have been carried out at CEA/Saclay after cold testing. IPP has also installed a vacuum tank to perform Paschen tests during the preparation of all the coils for assembly, including also the 20 planar coils which cannot be tested at the manufacturer Tesla. These tests have proven to be a powerful tool to detect hidden insulation defects and void/cavities in the primary impregnation system, which could not be detected otherwise with the standard high voltage tests. This paper will summarize the background and experience accumulated in about 2 years of Paschen tests on the W7-X coils, including a description of the equipment, main results and statistics, weak points detected and repaired on the coils, and possibilities of improvements in the development and production of the W7-X magnets. The importance and the need of Paschen tests as part of the acceptance procedure for superconducting magnets to be used in future projects will also be

  6. Modelling and analysis of flux surface mapping experiments on W7-X

    Science.gov (United States)

    Lazerson, Samuel; Otte, Matthias; Bozhenkov, Sergey; Sunn Pedersen, Thomas; Bräuer, Torsten; Gates, David; Neilson, Hutch; W7-X Team

    2015-11-01

    The measurement and compensation of error fields in W7-X will be key to the device achieving high beta steady state operations. Flux surface mapping utilizes the vacuum magnetic flux surfaces, a feature unique to stellarators and heliotrons, to allow direct measurement of magnetic topology, and thereby allows a highly accurate determination of remnant magnetic field errors. As will be reported separately at this meeting, the first measurements confirming the existence of nested flux surfaces in W7-X have been made. In this presentation, a synthetic diagnostic for the flux surface mapping diagnostic is presented. It utilizes Poincaré traces to construct an image of the flux surface consistent with the measured camera geometry, fluorescent rod sweep plane, and emitter beam position. Forward modeling of the high-iota configuration will be presented demonstrating an ability to measure the intrinsic error field using the U.S. supplied trim coil system on W7-X, and a first experimental assessment of error fields in W7-X will be presented. This work has been authored by Princeton University under Contract Number DE-AC02-09CH11466 with the US Department of Energy.

  7. Immobilisation in cement of ion exchange resins arising from the purification of reagents used for the decontamination of reactor circuits

    International Nuclear Information System (INIS)

    Howard, C.G.; Jolliffe, C.; Lee, D.J.

    1988-04-01

    The aim of the programme is to show that ion exchange resins used to remove activity from decontaminating agents used in water reactors can be successfully immobilised in cement. To achieve this, blends of Ordinary Portland Cement and ground granulated Blast Furnace Slag (ratio 9:1) have been used. Improvements in the properties of the product and the waste loading of 50 w/o damp resin can be achieved using microsilica, a finely divided form of silicon dioxide, as an additive to the blended cement. This report contains data on the effects of anion resins, and mixed anion/cation resins, on the performance of the cemented product. The effects of organic acids, especially picolinic and formic acids, bound to anion resins have also been investigated. In addition, formulations developed have been assessed at commercial scale (200 litres of cemented product) for their process and product characteristics. The final part of the report deals with the long-term product performance of samples prepared from cation resins which are now nearly one year old. (author)

  8. Determination of 25 trace impurity elements in U3O8 by horizontal ICP-AES after separation with TBP levextrel resin chromatography

    International Nuclear Information System (INIS)

    Guan Jingsu; Shi Youqing; Gao Binghua; Liu Yingmei

    1988-01-01

    A method for the determination of Al, As, Ba, Be, Bi, Ca, Cd, Cu, Co, Cr, Fe, Mg, Mn, Mo, Ni, P, Pb, Ru, Sb, Sn, Sr, Ti, V, W and Zn 25 trace elements in U 3 O 8 is reported. The sample is dissolved in HNO 3 or HNO 3 -HCLO 4 -HF and the uranium is separated by TBP Levextrel resin chromatogyaphy. The impurity elements containing in the aquaous phase are determined by horizontal ICp-AES method. With a sample of 300 mg, the detection limit for all the 25 elements is in the range of 0.01∼5ppm, the recovery is in the range of 82∼ 121%, the determination precision (RSD) is less than ±13%. 18 trace elements in reference material of U 3 O 8 prepared in China are determined, the values obtained well with the values of overall median of accepted laboratory means

  9. Processing of the quench detection signals in W7-X

    International Nuclear Information System (INIS)

    Birus, Dietrich; Schneider, Matthias; Rummel, Thomas; Fricke, Marko; Petry, Klaus; Ebersoldt, Andreas

    2009-01-01

    The Wendelstein 7-X (W7-X) project uses superconductive coils for generation of the magnetic field to keep the plasma. One of the important safety systems is the protection against quench events. The quench detection system of W7-X protects the superconducting coils, the superconducting bus bar sections and the high temperature superconductor of the current leads against the damage because of a quench and against the high stress by a fast discharge of the magnet system. Therefore, the present design of the quench detection system (QDS) uses a two-stage safety concept for discharging the magnetic system. This paper describes the present design of the system assembly from the quench detection unit (QDU) for the detection of the quench to the quench detection interface (QDI) to implement the two-stage safety concept.

  10. Mechanical properties of dental resin composites by co-filling diatomite and nanosized silica particles

    Energy Technology Data Exchange (ETDEWEB)

    Wang Hua; Zhu Meifang [State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Donghua University, Shanghai 201620 (China); Li Yaogang [Engineering Research Center of Advanced Glasses Manufacturing Technology, MOE, Donghua University, Shanghai 201620 (China); Zhang Qinghong, E-mail: zhangqh@dhu.edu.cn [Engineering Research Center of Advanced Glasses Manufacturing Technology, MOE, Donghua University, Shanghai 201620 (China); Wang Hongzhi, E-mail: wanghz@dhu.edu.cn [State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Donghua University, Shanghai 201620 (China)

    2011-04-08

    The aim of this study was to investigate the mechanical property effects of co-filling dental resin composites with porous diatomite and nanosized silica particles (OX-50). The purification of raw diatomite by acid-leaching was conducted in a hot 5 M HCl solution at 80 deg. C for 12 h. Both diatomite and nanosized SiO{sub 2} were silanized with 3-methacryloxypropyltrimethoxysilane. The silanized inorganic particles were mixed into a dimethacrylate resin. Purified diatomite was characterized by X-ray diffraction, UV-vis diffuse reflectance spectroscopy and an N{sub 2} adsorption-desorption isotherm. Silanized inorganic particles were characterized using Fourier transform infrared spectroscopy and a thermogravimetric analysis. The mechanical properties of the composites were tested by three-point bending, compression and Vicker's microhardness. Scanning electron microscopy was used to show the cross-section morphologies of the composites. Silanization of diatomite and nanosized silica positively reinforced interactions between the resin matrix and the inorganic particles. The mechanical properties of the resin composites gradually increased with the addition of modified diatomite (m-diatomite). The fracture surfaces of the composites exhibited large fracture steps with the addition of m-diatomite. However, when the mass fraction of m-diatomite was greater than 21 wt.% with respect to modified nanosized silica (mOX-50) and constituted 70% of the resin composite by weight, the mechanical properties of the resin composites started to decline. Thus, the porous structure of diatomite appears to be a crucial factor to improve mechanical properties of resin composites.

  11. 41 CFR 50-203.8 - Hearing.

    Science.gov (United States)

    2010-07-01

    ... 41 Public Contracts and Property Management 1 2010-07-01 2010-07-01 true Hearing. 50-203.8 Section 50-203.8 Public Contracts and Property Management Other Provisions Relating to Public Contracts..., examine, and cross-examine witnesses and to introduce into the record documentary or other evidence. (f...

  12. Recovery of americium from slag and crucible wastes and its purification

    International Nuclear Information System (INIS)

    Michael, K.M.; Dabholkar, G.M.; Vijayan, K.; Ramamoorthy, N.; Narayanan, C.V.; Jambunathan, U.; Kapoor, S.C.

    1990-01-01

    A method of recovery and purification of americium-241 from slag waste streams is described. Extraction of Am from slag solution of 0.16 M HNO 3 was carried out by tri-n-butyl phosphate. After stripping with acetic acid, Am was precipitated at pH 1. This was followed by metathesis to remove Ca. Final separation of Pu from Am solution was achieved by anion exchange method using Dowex 1x4 anion exchange resin. Details of large scale recovery of Am from slag are also described. (author). 12 refs., 11 tabs., 1 fig

  13. The determination, by x-ray-fluorescence spectrometry, of gold and uranium on resin

    International Nuclear Information System (INIS)

    Jacobs, J.J.; Balaes, A.M.E.

    1983-01-01

    The problems encountered in the determination of gold and uranium that are present simultaneously in a sample of resin were considered, and new background positions, as well as correction factors for background lift and partial spectral overlap, were determined for use in the X-ray-fluorescence measurement of these elements. The agreement between the results obtained by the use of the X-ray-fluorescence method and those obtained by atomic-absorption spectrophotometry were found to be satisfactory. The relative standard deviation in the former measurements is 0,005 at a concentration of 1000 p.p.m., and the working range of the calibrations is 15 to 1000 p.p.m. These limits can be extended by further dilution of the sample. The limits of determination are 6 p.p.m. in the briquette prepared from a sample of resin and 18 p.p.m. in the sample when the maximum mass of the sample is 3 g. The procedure is intended primarily for use in the rapid determination of gold and uranium when no analyses for other elements are required. The time taken for the analysis is 2 hours for 10 samples when 6 standards are used. A computer programme that was developed for the processing of the data is appended as part of a laboratory method

  14. Using x-radiometry to count resin-bonded layers in aramid ballistic cloth composites

    International Nuclear Information System (INIS)

    Larsen, R.E.; Golis, M.J.

    1989-01-01

    The army paratroopers and support ground troops (PASGT) helmet is a composite consisting of nominally 19 layers thickness aramid ballistic cloth heat-bonded in a press with rolled-on phenolic resin. Inadvertent omission or poor fitting of layers during hot pressing can significantly weaken the helmet and thereby drastically impair its effectiveness under combat conditions. Currently, helmets are accepted or rejected on a lot basis using ballistic projectile penetration destructive tests on a statistically significant sample from each lot. A Phase I small business innovative research (SBIR) was performed to access the feasibility of nondestructively counting layers by through-transmission x-radiometry, a technique that would allow 100 percent testing of helmets for layer count if proved feasible. Tests were conducted on flat panels, crown panels containing gaps, and actual helmets using 14-18 keV Pu x-rays from a 30-mCi Cm-244 source, a sodium iodide scintillation counter, several collimators, and a multichannel analyzer. The infusing of resin into artificially produced lateral gaps in the crown specimen and into actual lateral gaps in the helmet during press-curing impaired the effectiveness of the radiometric method by introducing high radiometric density material into the beam path. It is concluded that radiometry should be combined with visual inspection to assure helmet integrity. Modified approaches are discussed

  15. Ag@Ag{sub 8}W{sub 4}O{sub 16} nanoroasted rice beads with photocatalytic, antibacterial and anticancer activity

    Energy Technology Data Exchange (ETDEWEB)

    Selvamani, Muthamizh; Krishnamoorthy, Giribabu; Ramadoss, Manigandan; Sivakumar, Praveen Kumar; Settu, Munusamy [Department of Inorganic Chemistry, University of Madras, Guindy Campus, Chennai, 600 025 (India); Ranganathan, Suresh [Department of Chemistry, SRM University, Ramapuram Campus, Chennai, 600 089 (India); Vengidusamy, Narayanan, E-mail: vnnara@yahoo.co.in [Department of Inorganic Chemistry, University of Madras, Guindy Campus, Chennai, 600 025 (India)

    2016-03-01

    Increasing resistance of pathogens and cancer cell line towards antibiotics and anticancer agents has caused serious health problems in the past decades. Due to these problems in recent years, researchers have tried to combine nanotechnology with material science to have intrinsic antimicrobial and anticancer activity. The metals and metal oxides were investigated with respect to their antimicrobial and anticancer effects towards bacteria and cancer cell line. In the present work metal@metal tungstate (Ag@Ag{sub 8}W{sub 4}O{sub 16} nanoroasted rice beads) is investigated for antibacterial activity against Escherichia coli and Staphylococcus aureus using Mueller-Hinton broth and the anticancer activity against B16F10 cell line was studied. Silver decorated silver tungstate (Ag@Ag{sub 8}W{sub 4}O{sub 16}) was synthesized by the microwave irradiation method using Cetyl Trimethyl Ammonium Bromide (CTAB). Ag@Ag{sub 8}W{sub 4}O{sub 16} was characterized by using various spectroscopic techniques. The phase and crystalline nature were analyzed by using XRD. The morphological analysis was carried out using Field Emission Scanning Electron Microscopy (FE-SEM), and High Resolution Transmission Electron Microscopy (HR-TEM). Further, Fourier Transform Infrared Spectroscopy (FT-IR) and Raman spectral analysis were carried out in order to ascertain the presence of functional groups in Ag@Ag{sub 8}W{sub 4}O{sub 16}. The optical property was investigated using Diffuse Reflectance Ultraviolet–Visible Spectroscopy (DRS-UV–Vis) and the band gap was found to be 3.08 eV. Surface area of the synthesized Ag@Ag{sub 8}W{sub 4}O{sub 16} wasanalyzed by BET analysis and Ag@Ag{sub 8}W{sub 4}O{sub 16} was utilized for the degradation of organic dyes methylene blue and rhodamine B. The morphology of the Ag@Ag{sub 8}W{sub 4}O{sub 16} resembles roasted rice beads with breath and length in nm range. The oxidation state of tungsten (W) and silver (Ag) was investigated using X-ray photoelectron

  16. Nanomechanical properties of dental resin-composites.

    Science.gov (United States)

    El-Safty, S; Akhtar, R; Silikas, N; Watts, D C

    2012-12-01

    To determine by nanoindentation the hardness and elastic modulus of resin-composites, including a series with systematically varied filler loading, plus other representative materials that fall into the categories of flowable, bulk-fill and conventional nano-hybrid types. Ten dental resin-composites: three flowable, three bulk-fill and four conventional were investigated using nanoindentation. Disc specimens (15mm×2mm) were prepared from each material using a metallic mold. Specimens were irradiated in the mold at top and bottom surfaces in multiple overlapping points (40s each) with light curing unit at 650mW/cm(2). Specimens were then mounted in 3cm diameter phenolic ring forms and embedded in a self-curing polystyrene resin. After grinding and polishing, specimens were stored in distilled water at 37°C for 7 days. Specimens were investigated using an Agilent Technologies XP nanoindenter equipped with a Berkovich diamond tip (100nm radius). Each specimen was loaded at one loading rate and three different unloading rates (at room temperature) with thirty indentations, per unloading rate. The maximum load applied by the nanoindenter to examine the specimens was 10mN. Dependent on the type of the resin-composite material, the mean values ranged from 0.73GPa to 1.60GPa for nanohardness and from 14.44GPa to 24.07GPa for elastic modulus. There was a significant positive non-linear correlation between elastic modulus and nanohardness (r(2)=0.88). Nonlinear regression revealed a significant positive correlation (r(2)=0.62) between elastic moduli and filler loading and a non-significant correlation (r(2)=0.50) between nanohardness and filler loading of the studied materials. Varying the unloading rates showed no consistent effect on the elastic modulus and nanohardness of the studied materials. For a specific resin matrix, both elastic moduli and nanohardness correlated positively with filler loading. For the resin-composites investigated, the group-average elastic

  17. The structural, electronic and magnetic properties of Ga{sub 8x}Mn{sub x}As{sub 8} clusters

    Energy Technology Data Exchange (ETDEWEB)

    Gu, Gangxu [College of Physical Science and Technology, Sichuan University, Chengdu 610064 (China); Key Laboratory of High Energy Density Physics and Technology of Ministry of Education, Sichuan University, Chengdu 610064 (China); Xiang, Gang, E-mail: gxiang@scu.edu.cn [College of Physical Science and Technology, Sichuan University, Chengdu 610064 (China); Key Laboratory of High Energy Density Physics and Technology of Ministry of Education, Sichuan University, Chengdu 610064 (China); Luo, Jia; Tang, Zhijie [College of Physical Science and Technology, Sichuan University, Chengdu 610064 (China); Key Laboratory of High Energy Density Physics and Technology of Ministry of Education, Sichuan University, Chengdu 610064 (China); Zhang, Xi, E-mail: xizhang@scu.edu.cn [College of Physical Science and Technology, Sichuan University, Chengdu 610064 (China); Key Laboratory of High Energy Density Physics and Technology of Ministry of Education, Sichuan University, Chengdu 610064 (China)

    2015-06-15

    We systematically investigate the ground-state magnetic properties of Ga{sub 8x}Mn{sub x}As{sub 8} clusters (x=0, 2, 4, 6, and 8) within the framework of density functional theory (DFT) using a strategy that successively adopts the particle swarm optimization (CALYPSO) code and fixed spin-moment (FSM) method. The results show that for Ga{sub 8x}Mn{sub x}As{sub 8} in the ground states or low-lying isomers, Mn atoms tend to assemble at the core of the clusters and the ferrimagnetic Mn–Mn couplings are identified for Ga{sub 8x}Mn{sub x}As{sub 8} (x=4, 6, and 8), while Ga{sub 8}As{sub 8} and Ga{sub 6}Mn{sub 2}As{sub 8} are nonmagnetic. The possibility of multiple ground states of Ga{sub 8x}Mn{sub x}As{sub 8} (x=4, 6, and 8) is also demonstrated. The binding energy and LUMO–HOMO gap analysis show that Ga{sub 8x}Mn{sub x}As{sub 8} clusters with large x are more likely synthesized and exhibit stronger chemical reactivity. - Highlights: • The ground-state structural and magnetic configurations of Ga{sub 8-x}Mn{sub x}As{sub 8} clusters are predicted by using the particle swarm optimization (CALYPSO) code and fixed spin-moment method. • For the ground state and low-lying isomers of Ga{sub 8x}Mn{sub x}As{sub 8} clusters, Mn atoms are gathered at the core of cluster, and ferrimagnetic Mn–Mn coupling is found. • Ga{sub 8x}Mn{sub x}As{sub 8} with large x is more likely formed and reacts with each other to create larger clusters.

  18. Transition of W7-X non-planar coils from manufacturing to assembly

    Energy Technology Data Exchange (ETDEWEB)

    Ehrke, G. [Max-Planck-Institut fuer Plasmaphysik (IPP), EURATOM Association, Wendelsteinstrasse 1, D-17491 Greifswald (Germany)], E-mail: gunnar.ehrke@ipp.mpg.de

    2009-06-15

    The main magnetic field of Wendelstein 7-X fusion experiment (W7-X) at Max-Planck-Institut fuer Plasmaphysik Greifswald, Germany will be provided by 50 non-planar coils and supported by 20 planar coils. The non-planar coils were delivered by a consortium (CON) consisting of Babcock Noell GmbH Germany (BNG) and ASG Superconductors S.p.A. Italy (ASG). The coil production ended with the delivery of the last non-planar coil in March 2008 at the manufacturing branch of BNG in Zeitz, Germany. The construction of the coils was characterised by design changes, many rework actions and resulting time delays. Due to these numerous adjustments and changes a continuous improvement process was needed. This paper will give an overview about the transition of the non-planar coils from the acceptance tests at the manufacturer site to the beginning of the assembly at IPP. Furthermore this report will highlight technical interfaces in the period of transition.

  19. A critical analysis of the degree of conversion of resin-based luting cements

    Science.gov (United States)

    NORONHA FILHO, Jaime Dutra; BRANDÃO, Natasha Lamego; POSKUS, Laiza Tatiana; GUIMARÃES, José Guilherme Antunes; da SILVA, Eduardo Moreira

    2010-01-01

    Objective This study analyzed the degree of conversion (DC%) of four resin-based cements (All Ceram, Enforce, Rely X ARC and Variolink II) activated by two modes (chemical and dual), and evaluated the decrease of DC% in the dual mode promoted by the interposition of a 2.0-mm-thick IPS Empress 2 disc. Material and Methods In the chemical activation, the resin-based cements were prepared by mixing equal amounts of base and catalyst pastes. In the dual activation, after mixing, the cements were light-activated at 650 mW/cm2 for 40 s. In a third group, the cements were lightactivated through a 2.0-mm-thick IPS Empress 2 disc. The DC% was evaluated in a FT-IR spectrometer equipped with an attenuated total reflectance crystal (ATR). The data were analyzed by two-way ANOVA and Tukey's HSD test. Results For all resin-based cements, the DC% was significantly higher with dual activation, followed by dual activation through IPS Empress 2, and chemical activation (pEmpress 2 disc (pEmpress 2. PMID:21085798

  20. ECRH and ECCD scenarios for W7-X

    Directory of Open Access Journals (Sweden)

    Laqua H.P.

    2012-09-01

    Full Text Available The main ECRH scenarios for the W7-X Stellarator are described. Both X2 (low and moderate densities and O2 scenarios (high density have been studied. Since O2 scenario cannot be realized without pre-heating, transition from X2 to O2 scenarios has been discussed. Due to a lack of Ohmic transformer, only ECCD is available for compensating the bootstrap current and for controlling the edge rotational transform value. The efficiency of ECCD for all main scenarios has been estimated. All simulations have been performed by a 1D transport code coupled self-consistently with ray-tracing code.

  1. Study of Moessbauer effect on LiFe5-x Alx O8, LiFe 5-x Gax O8 and LiGa5-x Fex O8 systems

    International Nuclear Information System (INIS)

    Barthem, V.M.T.S.

    1982-01-01

    The measures obtained by Moessbauer spectroscopy from LiFe 5-x Ga x O 8 and LiFe 5-x Al x O 8 systems are presented. A comparative study of the influences of dopant diamagnetic ions on magnetic structures of lithium ferrite was performed. The LiGa 5-x Fe x O 8 systems were analysed based on the existing data from LiAl 5-x Fe x O 8 systems, otaining informations about the iron ion behaviour in both matrices. (M.C.K.) [pt

  2. The chemical speciation of 137Cs in sheepmeat

    International Nuclear Information System (INIS)

    Pang, T.Y.M.; Taylor, D.M.; Williams, D.R.

    1996-01-01

    Minced sheep muscle, homogenised liver and fragmented rib or cortical bone, from sheep grazing near Bootle, Cumbria, U.K., which had been stored for some months at -20 o C, were extracted at 4 o C with an isotonic 0.15 M NaCl-0.02 M phosphate buffer at pH 7.4. Each successive extraction released about 50% of the total 137 Cs remaining in the tissue. Passage of the extracts through a column of the cation-exchanger Dowex 50 x 8 indicated that essentially all the extracted 137 Cs was in cationic form. (author)

  3. Measurement of exclusive $\\gamma\\gamma\\rightarrow W^+W^-$ production and search for exclusive Higgs boson production in $pp$ collisions at $\\sqrt{s} = 8$ TeV using the ATLAS detector

    CERN Document Server

    Aaboud, Morad; Abbott, Brad; Abdallah, Jalal; Abdinov, Ovsat; Abeloos, Baptiste; Aben, Rosemarie; AbouZeid, Ossama; Abraham, Nicola; Abramowicz, Halina; Abreu, Henso; Abreu, Ricardo; Abulaiti, Yiming; Acharya, Bobby Samir; Adamczyk, Leszek; Adams, David; Adelman, Jahred; Adomeit, Stefanie; Adye, Tim; Affolder, Tony; Agatonovic-Jovin, Tatjana; Agricola, Johannes; Aguilar-Saavedra, Juan Antonio; Ahlen, Steven; Ahmadov, Faig; Aielli, Giulio; Akerstedt, Henrik; Åkesson, Torsten Paul Ake; Akimov, Andrei; Alberghi, Gian Luigi; Albert, Justin; Albrand, Solveig; Alconada Verzini, Maria Josefina; Aleksa, Martin; Aleksandrov, Igor; Alexa, Calin; Alexander, Gideon; Alexopoulos, Theodoros; Alhroob, Muhammad; Ali, Babar; Aliev, Malik; Alimonti, Gianluca; Alison, John; Alkire, Steven Patrick; Allbrooke, Benedict; Allen, Benjamin William; Allport, Phillip; Aloisio, Alberto; Alonso, Alejandro; Alonso, Francisco; Alpigiani, Cristiano; Alstaty, Mahmoud; Alvarez Gonzalez, Barbara; Άlvarez Piqueras, Damián; 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Åsman, Barbro; Asquith, Lily; Assamagan, Ketevi; Astalos, Robert; Atkinson, Markus; Atlay, Naim Bora; Augsten, Kamil; Avolio, Giuseppe; Axen, Bradley; Ayoub, Mohamad Kassem; Azuelos, Georges; Baak, Max; Baas, Alessandra; Baca, Matthew John; Bachacou, Henri; Bachas, Konstantinos; Backes, Moritz; Backhaus, Malte; Bagiacchi, Paolo; Bagnaia, Paolo; Bai, Yu; Baines, John; Baker, Oliver Keith; Baldin, Evgenii; Balek, Petr; Balestri, Thomas; Balli, Fabrice; Balunas, William Keaton; Banas, Elzbieta; Banerjee, Swagato; Bannoura, Arwa A E; Barak, Liron; Barberio, Elisabetta Luigia; Barberis, Dario; Barbero, Marlon; Barillari, Teresa; Barisits, Martin-Stefan; Barklow, Timothy; Barlow, Nick; Barnes, Sarah Louise; Barnett, Bruce; Barnett, Michael; Barnovska, Zuzana; Baroncelli, Antonio; Barone, Gaetano; Barr, Alan; Barranco Navarro, Laura; Barreiro, Fernando; Barreiro Guimarães da Costa, João; Bartoldus, Rainer; Barton, Adam Edward; Bartos, Pavol; Basalaev, Artem; Bassalat, Ahmed; Bates, Richard; Batista, Santiago Juan; 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Bogaerts, Joannes Andreas; Bogavac, Danijela; Bogdanchikov, Alexander; Bohm, Christian; Boisvert, Veronique; Bokan, Petar; Bold, Tomasz; Boldyrev, Alexey; Bomben, Marco; Bona, Marcella; Boonekamp, Maarten; Borisov, Anatoly; Borissov, Guennadi; Bortfeldt, Jonathan; Bortoletto, Daniela; Bortolotto, Valerio; Bos, Kors; Boscherini, Davide; Bosman, Martine; Bossio Sola, Jonathan David; Boudreau, Joseph; Bouffard, Julian; Bouhova-Thacker, Evelina Vassileva; Boumediene, Djamel Eddine; Bourdarios, Claire; Boutle, Sarah Kate; Boveia, Antonio; Boyd, James; Boyko, Igor; Bracinik, Juraj; Brandt, Andrew; Brandt, Gerhard; Brandt, Oleg; Bratzler, Uwe; Brau, Benjamin; Brau, James; Braun, Helmut; Breaden Madden, William Dmitri; Brendlinger, Kurt; Brennan, Amelia Jean; Brenner, Lydia; Brenner, Richard; Bressler, Shikma; Bristow, Timothy Michael; Britton, Dave; Britzger, Daniel; Brochu, Frederic; Brock, Ian; Brock, Raymond; Brooijmans, Gustaaf; Brooks, Timothy; Brooks, William; Brosamer, Jacquelyn; Brost, Elizabeth; 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Gecse, Zoltan; Gee, Norman; Geich-Gimbel, Christoph; Geisen, Marc; Geisler, Manuel Patrice; Gemme, Claudia; Genest, Marie-Hélène; Geng, Cong; Gentile, Simonetta; Gentsos, Christos; George, Simon; Gerbaudo, Davide; Gershon, Avi; Ghasemi, Sara; Ghazlane, Hamid; Ghneimat, Mazuza; Giacobbe, Benedetto; Giagu, Stefano; Giannetti, Paola; Gibbard, Bruce; Gibson, Stephen; Gignac, Matthew; Gilchriese, Murdock; Gillam, Thomas; Gillberg, Dag; Gilles, Geoffrey; Gingrich, Douglas; Giokaris, Nikos; Giordani, MarioPaolo; Giorgi, Filippo Maria; Giorgi, Francesco Michelangelo; Giraud, Pierre-Francois; Giromini, Paolo; Giugni, Danilo; Giuli, Francesco; Giuliani, Claudia; Giulini, Maddalena; Gjelsten, Børge Kile; Gkaitatzis, Stamatios; Gkialas, Ioannis; Gkougkousis, Evangelos Leonidas; Gladilin, Leonid; Glasman, Claudia; Glatzer, Julian; Glaysher, Paul; Glazov, Alexandre; Goblirsch-Kolb, Maximilian; Godlewski, Jan; Goldfarb, Steven; Golling, Tobias; Golubkov, Dmitry; Gomes, Agostinho; Gonçalo, Ricardo; Goncalves Pinto Firmino Da Costa, Joao; Gonella, Giulia; Gonella, Laura; Gongadze, Alexi; González de la Hoz, Santiago; Gonzalez Parra, Garoe; Gonzalez-Sevilla, Sergio; Goossens, Luc; Gorbounov, Petr Andreevich; Gordon, Howard; Gorelov, Igor; Gorini, Benedetto; Gorini, Edoardo; Gorišek, Andrej; Gornicki, Edward; Goshaw, Alfred; Gössling, Claus; Gostkin, Mikhail Ivanovitch; Goudet, Christophe Raymond; Goujdami, Driss; Goussiou, Anna; Govender, Nicolin; Gozani, Eitan; Graber, Lars; Grabowska-Bold, Iwona; Gradin, Per Olov Joakim; Grafström, Per; Gramling, Johanna; Gramstad, Eirik; Grancagnolo, Sergio; Gratchev, Vadim; Gravila, Paul Mircea; Gray, Heather; Graziani, Enrico; Greenwood, Zeno Dixon; Grefe, Christian; Gregersen, Kristian; Gregor, Ingrid-Maria; Grenier, Philippe; Grevtsov, Kirill; Griffiths, Justin; Grillo, Alexander; Grimm, Kathryn; Grinstein, Sebastian; Gris, Philippe Luc Yves; Grivaz, Jean-Francois; Groh, Sabrina; Grohs, Johannes Philipp; Gross, Eilam; Grosse-Knetter, Joern; Grossi, Giulio Cornelio; Grout, Zara Jane; Guan, Liang; Guan, Wen; Guenther, Jaroslav; Guescini, Francesco; Guest, Daniel; Gueta, Orel; Guido, Elisa; Guillemin, Thibault; Guindon, Stefan; Gul, Umar; Gumpert, Christian; Guo, Jun; Guo, Yicheng; Gupta, Ruchi; Gupta, Shaun; Gustavino, Giuliano; Gutierrez, Phillip; Gutierrez Ortiz, Nicolas Gilberto; Gutschow, Christian; Guyot, Claude; Gwenlan, Claire; Gwilliam, Carl; Haas, Andy; Haber, Carl; Hadavand, Haleh Khani; Haddad, Nacim; Hadef, Asma; Hageböck, Stephan; Hajduk, Zbigniew; Hakobyan, Hrachya; Haleem, Mahsana; Haley, Joseph; Halladjian, Garabed; Hallewell, Gregory David; Hamacher, Klaus; Hamal, Petr; Hamano, Kenji; Hamilton, Andrew; Hamity, Guillermo Nicolas; Hamnett, Phillip George; Han, Liang; Hanagaki, Kazunori; Hanawa, Keita; Hance, Michael; Haney, Bijan; Hanisch, Stefanie; Hanke, Paul; Hanna, Remie; Hansen, Jørgen Beck; Hansen, Jorn Dines; Hansen, Maike Christina; Hansen, Peter Henrik; Hara, Kazuhiko; Hard, Andrew; Harenberg, Torsten; Hariri, Faten; Harkusha, Siarhei; Harrington, Robert; Harrison, Paul Fraser; Hartjes, Fred; Hartmann, Nikolai Marcel; Hasegawa, Makoto; Hasegawa, Yoji; Hasib, A; Hassani, Samira; Haug, Sigve; Hauser, Reiner; Hauswald, Lorenz; Havranek, Miroslav; Hawkes, Christopher; Hawkings, Richard John; Hayakawa, Daiki; Hayden, Daniel; Hays, Chris; Hays, Jonathan Michael; Hayward, Helen; Haywood, Stephen; Head, Simon; Heck, Tobias; Hedberg, Vincent; Heelan, Louise; Heim, Sarah; Heim, Timon; Heinemann, Beate; Heinrich, Jochen Jens; Heinrich, Lukas; Heinz, Christian; Hejbal, Jiri; Helary, Louis; Hellman, Sten; Helsens, Clement; Henderson, James; Henderson, Robert; Heng, Yang; Henkelmann, Steffen; Henriques Correia, Ana Maria; Henrot-Versille, Sophie; Herbert, Geoffrey Henry; Herget, Verena; Hernández Jiménez, Yesenia; Herten, Gregor; Hertenberger, Ralf; Hervas, Luis; Hesketh, Gavin Grant; Hessey, Nigel; Hetherly, Jeffrey Wayne; Hickling, Robert; Higón-Rodriguez, Emilio; Hill, Ewan; Hill, John; Hiller, Karl Heinz; Hillier, Stephen; Hinchliffe, Ian; Hines, Elizabeth; Hinman, Rachel Reisner; Hirose, Minoru; Hirschbuehl, Dominic; Hobbs, John; Hod, Noam; Hodgkinson, Mark; Hodgson, Paul; Hoecker, Andreas; Hoeferkamp, Martin; Hoenig, Friedrich; Hohn, David; Holmes, Tova Ray; Homann, Michael; Hong, Tae Min; Hooberman, Benjamin Henry; Hopkins, Walter; Horii, Yasuyuki; Horton, Arthur James; Hostachy, Jean-Yves; Hou, Suen; Hoummada, Abdeslam; Howarth, James; Hrabovsky, Miroslav; Hristova, Ivana; Hrivnac, Julius; Hryn'ova, Tetiana; Hrynevich, Aliaksei; Hsu, Catherine; Hsu, Pai-hsien Jennifer; Hsu, Shih-Chieh; Hu, Diedi; Hu, Qipeng; Hu, Shuyang; Huang, Yanping; Hubacek, Zdenek; Hubaut, Fabrice; Huegging, Fabian; Huffman, Todd Brian; Hughes, Emlyn; Hughes, Gareth; Huhtinen, Mika; Huo, Peng; Huseynov, Nazim; Huston, Joey; Huth, John; Iacobucci, Giuseppe; Iakovidis, Georgios; Ibragimov, Iskander; Iconomidou-Fayard, Lydia; Ideal, Emma; Idrissi, Zineb; Iengo, Paolo; Igonkina, Olga; Iizawa, Tomoya; Ikegami, Yoichi; Ikeno, Masahiro; Ilchenko, Iurii; Iliadis, Dimitrios; Ilic, Nikolina; Ince, Tayfun; Introzzi, Gianluca; Ioannou, Pavlos; Iodice, Mauro; Iordanidou, Kalliopi; Ippolito, Valerio; Ishijima, Naoki; Ishino, Masaya; Ishitsuka, Masaki; Ishmukhametov, Renat; Issever, Cigdem; Istin, Serhat; Ito, Fumiaki; Iturbe Ponce, Julia Mariana; Iuppa, Roberto; Iwanski, Wieslaw; Iwasaki, Hiroyuki; Izen, Joseph; Izzo, Vincenzo; Jabbar, Samina; Jackson, Brett; Jackson, Paul; Jain, Vivek; Jakobi, Katharina Bianca; Jakobs, Karl; Jakobsen, Sune; Jakoubek, Tomas; Jamin, David Olivier; Jana, Dilip; Jansen, Eric; Jansky, Roland; Janssen, Jens; Janus, Michel; Jarlskog, Göran; Javadov, Namig; Javůrek, Tomáš; Jeanneau, Fabien; Jeanty, Laura; Jejelava, Juansher; Jeng, Geng-yuan; Jennens, David; Jenni, Peter; Jeske, Carl; Jézéquel, Stéphane; Ji, Haoshuang; Jia, Jiangyong; Jiang, Hai; Jiang, Yi; Jiggins, Stephen; Jimenez Pena, Javier; Jin, Shan; Jinaru, Adam; Jinnouchi, Osamu; Johansson, Per; Johns, Kenneth; Johnson, William Joseph; Jon-And, Kerstin; Jones, Graham; Jones, Roger; Jones, Sarah; Jones, Tim; Jongmanns, Jan; Jorge, Pedro; Jovicevic, Jelena; Ju, Xiangyang; Juste Rozas, Aurelio; Köhler, Markus Konrad; Kaczmarska, Anna; Kado, Marumi; Kagan, Harris; Kagan, Michael; Kahn, Sebastien Jonathan; Kaji, Toshiaki; Kajomovitz, Enrique; Kalderon, Charles William; Kaluza, Adam; Kama, Sami; Kamenshchikov, Andrey; Kanaya, Naoko; Kaneti, Steven; Kanjir, Luka; Kantserov, Vadim; Kanzaki, Junichi; Kaplan, Benjamin; Kaplan, Laser Seymour; Kapliy, Anton; Kar, Deepak; Karakostas, Konstantinos; Karamaoun, Andrew; Karastathis, Nikolaos; Kareem, Mohammad Jawad; Karentzos, Efstathios; Karnevskiy, Mikhail; Karpov, Sergey; Karpova, Zoya; Karthik, Krishnaiyengar; Kartvelishvili, Vakhtang; Karyukhin, Andrey; Kasahara, Kota; Kashif, Lashkar; Kass, Richard; Kastanas, Alex; Kataoka, Yousuke; Kato, Chikuma; Katre, Akshay; Katzy, Judith; Kawagoe, Kiyotomo; Kawamoto, Tatsuo; Kawamura, Gen; Kazanin, Vassili; Keeler, Richard; Kehoe, Robert; Keller, John; Kempster, Jacob Julian; Kentaro, Kawade; Keoshkerian, Houry; Kepka, Oldrich; Kerševan, Borut Paul; Kersten, Susanne; Keyes, Robert; Khader, Mazin; Khalil-zada, Farkhad; Khanov, Alexander; Kharlamov, Alexey; Khoo, Teng Jian; Khovanskiy, Valery; Khramov, Evgeniy; Khubua, Jemal; Kido, Shogo; Kilby, Callum; Kim, Hee Yeun; Kim, Shinhong; Kim, Young-Kee; Kimura, Naoki; Kind, Oliver Maria; King, Barry; King, Matthew; King, Samuel Burton; Kirk, Julie; Kiryunin, Andrey; Kishimoto, Tomoe; Kisielewska, Danuta; Kiss, Florian; Kiuchi, Kenji; Kivernyk, Oleh; Kladiva, Eduard; Klein, Matthew Henry; Klein, Max; Klein, Uta; Kleinknecht, Konrad; Klimek, Pawel; Klimentov, Alexei; Klingenberg, Reiner; Klinger, Joel Alexander; Klioutchnikova, Tatiana; Kluge, Eike-Erik; Kluit, Peter; Kluth, Stefan; Knapik, Joanna; Kneringer, Emmerich; Knoops, Edith; Knue, Andrea; Kobayashi, Aine; Kobayashi, Dai; Kobayashi, Tomio; Kobel, Michael; Kocian, Martin; Kodys, Peter; Koehler, Nicolas Maximilian; Koffas, Thomas; Koffeman, Els; Koi, Tatsumi; Kolanoski, Hermann; Kolb, Mathis; Koletsou, Iro; Komar, Aston; Komori, Yuto; Kondo, Takahiko; Kondrashova, Nataliia; Köneke, Karsten; König, Adriaan; Kono, Takanori; Konoplich, Rostislav; Konstantinidis, Nikolaos; Kopeliansky, Revital; Koperny, Stefan; Köpke, Lutz; Kopp, Anna Katharina; Korcyl, Krzysztof; Kordas, Kostantinos; Korn, Andreas; Korol, Aleksandr; Korolkov, Ilya; Korolkova, Elena; Kortner, Oliver; Kortner, Sandra; Kosek, Tomas; Kostyukhin, Vadim; Kotwal, Ashutosh; Kourkoumeli-Charalampidi, Athina; Kourkoumelis, Christine; Kouskoura, Vasiliki; Kowalewska, Anna Bozena; Kowalewski, Robert Victor; Kowalski, Tadeusz; Kozakai, Chihiro; Kozanecki, Witold; Kozhin, Anatoly; Kramarenko, Viktor; Kramberger, Gregor; Krasnopevtsev, Dimitriy; Krasny, Mieczyslaw Witold; Krasznahorkay, Attila; Kravchenko, Anton; Kretz, Moritz; Kretzschmar, Jan; Kreutzfeldt, Kristof; Krieger, Peter; Krizka, Karol; Kroeninger, Kevin; Kroha, Hubert; Kroll, Joe; Kroseberg, Juergen; Krstic, Jelena; Kruchonak, Uladzimir; Krüger, Hans; Krumnack, Nils; Kruse, Amanda; Kruse, Mark; Kruskal, Michael; Kubota, Takashi; Kucuk, Hilal; Kuday, Sinan; Kuechler, Jan Thomas; Kuehn, Susanne; Kugel, Andreas; Kuger, Fabian; Kuhl, Andrew; Kuhl, Thorsten; Kukhtin, Victor; Kukla, Romain; Kulchitsky, Yuri; Kuleshov, Sergey; Kuna, Marine; Kunigo, Takuto; Kupco, Alexander; Kurashige, Hisaya; Kurochkin, Yurii; Kus, Vlastimil; Kuwertz, Emma Sian; Kuze, Masahiro; Kvita, Jiri; Kwan, Tony; Kyriazopoulos, Dimitrios; La Rosa, Alessandro; La Rosa Navarro, Jose Luis; La Rotonda, Laura; Lacasta, Carlos; Lacava, Francesco; Lacey, James; Lacker, Heiko; Lacour, Didier; Lacuesta, Vicente Ramón; Ladygin, Evgueni; Lafaye, Remi; Laforge, Bertrand; Lagouri, Theodota; Lai, Stanley; Lammers, Sabine; Lampl, Walter; Lançon, Eric; Landgraf, Ulrich; Landon, Murrough; Lanfermann, Marie Christine; Lang, Valerie Susanne; Lange, J örn Christian; Lankford, Andrew; Lanni, Francesco; Lantzsch, Kerstin; Lanza, Agostino; Laplace, Sandrine; Lapoire, Cecile; Laporte, Jean-Francois; Lari, Tommaso; Lasagni Manghi, Federico; Lassnig, Mario; Laurelli, Paolo; Lavrijsen, Wim; Law, Alexander; Laycock, Paul; Lazovich, Tomo; Lazzaroni, Massimo; Le, Brian; Le Dortz, Olivier; Le Guirriec, Emmanuel; Le Quilleuc, Eloi; LeBlanc, Matthew Edgar; LeCompte, Thomas; Ledroit-Guillon, Fabienne Agnes Marie; Lee, Claire Alexandra; Lee, Shih-Chang; Lee, Lawrence; Lefebvre, Benoit; Lefebvre, Guillaume; Lefebvre, Michel; Legger, Federica; Leggett, Charles; Lehan, Allan; Lehmann Miotto, Giovanna; Lei, Xiaowen; Leight, William Axel; Leisos, Antonios; Leister, Andrew Gerard; Leite, Marco Aurelio Lisboa; Leitner, Rupert; Lellouch, Daniel; Lemmer, Boris; Leney, Katharine; Lenz, Tatjana; Lenzi, Bruno; Leone, Robert; Leone, Sandra; Leonidopoulos, Christos; Leontsinis, Stefanos; Lerner, Giuseppe; Leroy, Claude; Lesage, Arthur; Lester, Christopher; Levchenko, Mikhail; Levêque, Jessica; Levin, Daniel; Levinson, Lorne; Levy, Mark; Lewis, Dave; Leyko, Agnieszka; Leyton, Michael; Li, Bing; Li, Changqiao; Li, Haifeng; Li, Ho Ling; Li, Lei; Li, Liang; Li, Qi; Li, Shu; Li, Xingguo; Li, Yichen; Liang, Zhijun; Liberti, Barbara; Liblong, Aaron; Lichard, Peter; Lie, Ki; Liebal, Jessica; Liebig, Wolfgang; Limosani, Antonio; Lin, Simon; Lin, Tai-Hua; Lindquist, Brian Edward; Lionti, Anthony Eric; Lipeles, Elliot; Lipniacka, Anna; Lisovyi, Mykhailo; Liss, Tony; Lister, Alison; Litke, Alan; Liu, Bo; Liu, Dong; Liu, Hao; Liu, Hongbin; Liu, Jian; Liu, Jianbei; Liu, Kun; Liu, Lulu; Liu, Miaoyuan; Liu, Minghui; Liu, Yanlin; Liu, Yanwen; Livan, Michele; Lleres, Annick; Llorente Merino, Javier; Lloyd, Stephen; Lo Sterzo, Francesco; Lobodzinska, Ewelina; Loch, Peter; Lockman, William; Loebinger, Fred; Loevschall-Jensen, Ask Emil; Loew, Kevin Michael; Loginov, Andrey; Lohse, Thomas; Lohwasser, Kristin; Lokajicek, Milos; Long, Brian Alexander; Long, Jonathan David; Long, Robin Eamonn; Longo, Luigi; Looper, Kristina Anne; Lopes, Lourenco; Lopez Mateos, David; Lopez Paredes, Brais; Lopez Paz, Ivan; Lopez Solis, Alvaro; Lorenz, Jeanette; Lorenzo Martinez, Narei; Losada, Marta; Lösel, Philipp Jonathan; Lou, XinChou; Lounis, Abdenour; Love, Jeremy; Love, Peter; Lu, Haonan; Lu, Nan; Lubatti, Henry; Luci, Claudio; Lucotte, Arnaud; Luedtke, Christian; Luehring, Frederick; Lukas, Wolfgang; Luminari, Lamberto; Lundberg, Olof; Lund-Jensen, Bengt; Luzi, Pierre Marc; Lynn, David; Lysak, Roman; Lytken, Else; Lyubushkin, Vladimir; Ma, Hong; Ma, Lian Liang; Ma, Yanhui; Maccarrone, Giovanni; Macchiolo, Anna; Macdonald, Calum Michael; Maček, Boštjan; Machado Miguens, Joana; Madaffari, Daniele; Madar, Romain; Maddocks, Harvey Jonathan; Mader, Wolfgang; Madsen, Alexander; Maeda, Junpei; Maeland, Steffen; Maeno, Tadashi; Maevskiy, Artem; Magradze, Erekle; Mahlstedt, Joern; Maiani, Camilla; Maidantchik, Carmen; Maier, Andreas Alexander; Maier, Thomas; Maio, Amélia; Majewski, Stephanie; Makida, Yasuhiro; Makovec, Nikola; Malaescu, Bogdan; Malecki, Pawel; Maleev, Victor; Malek, Fairouz; Mallik, Usha; Malon, David; Malone, Caitlin; Maltezos, Stavros; Malyukov, Sergei; Mamuzic, Judita; Mancini, Giada; Mandelli, Beatrice; Mandelli, Luciano; Mandić, Igor; Maneira, José; Manhaes de Andrade Filho, Luciano; Manjarres Ramos, Joany; Mann, Alexander; Manousos, Athanasios; Mansoulie, Bruno; Mansour, Jason Dhia; Mantifel, Rodger; Mantoani, Matteo; Manzoni, Stefano; Mapelli, Livio; Marceca, Gino; March, Luis; Marchiori, Giovanni; Marcisovsky, Michal; Marjanovic, Marija; Marley, Daniel; Marroquim, Fernando; Marsden, Stephen Philip; Marshall, Zach; Marti-Garcia, Salvador; Martin, Brian Thomas; Martin, Tim; Martin, Victoria Jane; Martin dit Latour, Bertrand; Martinez, Mario; Martinez Outschoorn, Verena; Martin-Haugh, Stewart; Martoiu, Victor Sorin; Martyniuk, Alex; Marx, Marilyn; Marzin, Antoine; Masetti, Lucia; Mashimo, Tetsuro; Mashinistov, Ruslan; Masik, Jiri; Maslennikov, Alexey; Massa, Ignazio; Massa, Lorenzo; Mastrandrea, Paolo; Mastroberardino, Anna; Masubuchi, Tatsuya; Mättig, Peter; Mattmann, Johannes; Maurer, Julien; Maxfield, Stephen; Maximov, Dmitriy; Mazini, Rachid; Mazza, Simone Michele; Mc Fadden, Neil Christopher; Mc Goldrick, Garrin; Mc Kee, Shawn Patrick; McCarn, Allison; McCarthy, Robert; McCarthy, Tom; McClymont, Laurie; McDonald, Emily; Mcfayden, Josh; Mchedlidze, Gvantsa; McMahon, Steve; McPherson, Robert; Medinnis, Michael; Meehan, Samuel; Mehlhase, Sascha; Mehta, Andrew; Meier, Karlheinz; Meineck, Christian; Meirose, Bernhard; Melini, Davide; Mellado Garcia, Bruce Rafael; Melo, Matej; Meloni, Federico; Mengarelli, Alberto; Menke, Sven; Meoni, Evelin; Mergelmeyer, Sebastian; Mermod, Philippe; Merola, Leonardo; Meroni, Chiara; Merritt, Frank; Messina, Andrea; Metcalfe, Jessica; Mete, Alaettin Serhan; Meyer, Carsten; Meyer, Christopher; Meyer, Jean-Pierre; Meyer, Jochen; Meyer Zu Theenhausen, Hanno; Miano, Fabrizio; Middleton, Robin; Miglioranzi, Silvia; Mijović, Liza; Mikenberg, Giora; Mikestikova, Marcela; Mikuž, Marko; Milesi, Marco; Milic, Adriana; Miller, David; Mills, Corrinne; Milov, Alexander; Milstead, David; Minaenko, Andrey; Minami, Yuto; Minashvili, Irakli; Mincer, Allen; Mindur, Bartosz; Mineev, Mikhail; Ming, Yao; Mir, Lluisa-Maria; Mistry, Khilesh; Mitani, Takashi; Mitrevski, Jovan; Mitsou, Vasiliki A; Miucci, Antonio; Miyagawa, Paul; Mjörnmark, Jan-Ulf; Moa, Torbjoern; Mochizuki, Kazuya; Mohapatra, Soumya; Molander, Simon; Moles-Valls, Regina; Monden, Ryutaro; Mondragon, Matthew Craig; Mönig, Klaus; Monk, James; Monnier, Emmanuel; Montalbano, Alyssa; Montejo Berlingen, Javier; Monticelli, Fernando; Monzani, Simone; Moore, Roger; Morange, Nicolas; Moreno, Deywis; Moreno Llácer, María; Morettini, Paolo; Mori, Daniel; Mori, Tatsuya; Morii, Masahiro; Morinaga, Masahiro; Morisbak, Vanja; Moritz, Sebastian; Morley, Anthony Keith; Mornacchi, Giuseppe; Morris, John; Mortensen, Simon Stark; Morvaj, Ljiljana; Mosidze, Maia; Moss, Josh; Motohashi, Kazuki; Mount, Richard; Mountricha, Eleni; Mouraviev, Sergei; Moyse, Edward; Muanza, Steve; Mudd, Richard; Mueller, Felix; Mueller, James; Mueller, Ralph Soeren Peter; Mueller, Thibaut; Muenstermann, Daniel; Mullen, Paul; Mullier, Geoffrey; Munoz Sanchez, Francisca Javiela; Murillo Quijada, Javier Alberto; Murray, Bill; Musheghyan, Haykuhi; Muškinja, Miha; Myagkov, Alexey; Myska, Miroslav; Nachman, Benjamin Philip; Nackenhorst, Olaf; Nagai, Koichi; Nagai, Ryo; Nagano, Kunihiro; Nagasaka, Yasushi; Nagata, Kazuki; Nagel, Martin; Nagy, Elemer; Nairz, Armin Michael; Nakahama, Yu; Nakamura, Koji; Nakamura, Tomoaki; Nakano, Itsuo; Namasivayam, Harisankar; Naranjo Garcia, Roger Felipe; Narayan, Rohin; Narrias Villar, Daniel Isaac; Naryshkin, Iouri; Naumann, Thomas; Navarro, Gabriela; Nayyar, Ruchika; Neal, Homer; Nechaeva, Polina; Neep, Thomas James; Negri, Andrea; Negrini, Matteo; Nektarijevic, Snezana; Nellist, Clara; Nelson, Andrew; Nemecek, Stanislav; Nemethy, Peter; Nepomuceno, Andre Asevedo; Nessi, Marzio; Neubauer, Mark; Neumann, Manuel; Neves, Ricardo; Nevski, Pavel; Newman, Paul; Nguyen, Duong Hai; Nguyen Manh, Tuan; Nickerson, Richard; Nicolaidou, Rosy; Nielsen, Jason; Nikiforov, Andriy; Nikolaenko, Vladimir; Nikolic-Audit, Irena; Nikolopoulos, Konstantinos; Nilsen, Jon Kerr; Nilsson, Paul; Ninomiya, Yoichi; Nisati, Aleandro; Nisius, Richard; Nobe, Takuya; Nodulman, Lawrence; Nomachi, Masaharu; Nomidis, Ioannis; Nooney, Tamsin; Norberg, Scarlet; Nordberg, Markus; Norjoharuddeen, Nurfikri; Novgorodova, Olga; Nowak, Sebastian; Nozaki, Mitsuaki; Nozka, Libor; Ntekas, Konstantinos; Nurse, Emily; Nuti, Francesco; O'grady, Fionnbarr; O'Neil, Dugan; O'Rourke, Abigail Alexandra; O'Shea, Val; Oakham, Gerald; Oberlack, Horst; Obermann, Theresa; Ocariz, Jose; Ochi, Atsuhiko; Ochoa, Ines; Ochoa-Ricoux, Juan Pedro; Oda, Susumu; Odaka, Shigeru; Ogren, Harold; Oh, Alexander; Oh, Seog; Ohm, Christian; Ohman, Henrik; Oide, Hideyuki; Okawa, Hideki; Okumura, Yasuyuki; Okuyama, Toyonobu; Olariu, Albert; Oleiro Seabra, Luis Filipe; Olivares Pino, Sebastian Andres; Oliveira Damazio, Denis; Olszewski, Andrzej; Olszowska, Jolanta; Onofre, António; Onogi, Kouta; Onyisi, Peter; Oreglia, Mark; Oren, Yona; Orestano, Domizia; Orlando, Nicola; Orr, Robert; Osculati, Bianca; Ospanov, Rustem; Otero y Garzon, Gustavo; Otono, Hidetoshi; Ouchrif, Mohamed; Ould-Saada, Farid; Ouraou, Ahmimed; Oussoren, Koen Pieter; Ouyang, Qun; Owen, Mark; Owen, Rhys Edward; Ozcan, Veysi Erkcan; Ozturk, Nurcan; Pachal, Katherine; Pacheco Pages, Andres; Pacheco Rodriguez, Laura; Padilla Aranda, Cristobal; Pagáčová, Martina; Pagan Griso, Simone; Paige, Frank; Pais, Preema; Pajchel, Katarina; Palacino, Gabriel; Palazzo, Serena; Palestini, Sandro; Palka, Marek; Pallin, Dominique; Panagiotopoulou, Evgenia; Pandini, Carlo Enrico; Panduro Vazquez, William; Pani, Priscilla; Panitkin, Sergey; Pantea, Dan; Paolozzi, Lorenzo; Papadopoulou, Theodora; Papageorgiou, Konstantinos; Paramonov, Alexander; Paredes Hernandez, Daniela; Parker, Adam Jackson; Parker, Michael Andrew; Parker, Kerry Ann; Parodi, Fabrizio; Parsons, John; Parzefall, Ulrich; Pascuzzi, Vincent; Pasqualucci, Enrico; Passaggio, Stefano; Pastore, Francesca; Pásztor, Gabriella; Pataraia, Sophio; Pater, Joleen; Pauly, Thilo; Pearce, James; Pearson, Benjamin; Pedersen, Lars Egholm; Pedersen, Maiken; Pedraza Lopez, Sebastian; Pedro, Rute; Peleganchuk, Sergey; Penc, Ondrej; Peng, Cong; Peng, Haiping; Penwell, John; Peralva, Bernardo; Perego, Marta Maria; Perepelitsa, Dennis; Perez Codina, Estel; Perini, Laura; Pernegger, Heinz; Perrella, Sabrina; Peschke, Richard; Peshekhonov, Vladimir; Peters, Krisztian; Peters, Yvonne; Petersen, Brian; Petersen, Troels; Petit, Elisabeth; Petridis, Andreas; Petridou, Chariclia; Petroff, Pierre; Petrolo, Emilio; Petrov, Mariyan; Petrucci, Fabrizio; Pettersson, Nora Emilia; Peyaud, Alan; Pezoa, Raquel; Phillips, Peter William; Piacquadio, Giacinto; Pianori, Elisabetta; Picazio, Attilio; Piccaro, Elisa; Piccinini, Maurizio; Pickering, Mark Andrew; Piegaia, Ricardo; Pilcher, James; Pilkington, Andrew; Pin, Arnaud Willy J; Pinamonti, Michele; Pinfold, James; Pingel, Almut; Pires, Sylvestre; Pirumov, Hayk; Pitt, Michael; Plazak, Lukas; Pleier, Marc-Andre; Pleskot, Vojtech; Plotnikova, Elena; Plucinski, Pawel; Pluth, Daniel; Poettgen, Ruth; Poggioli, Luc; Pohl, David-leon; Polesello, Giacomo; Poley, Anne-luise; Policicchio, Antonio; Polifka, Richard; Polini, Alessandro; Pollard, Christopher Samuel; Polychronakos, Venetios; Pommès, Kathy; Pontecorvo, Ludovico; Pope, Bernard; Popeneciu, Gabriel Alexandru; Popovic, Dragan; Poppleton, Alan; Pospisil, Stanislav; Potamianos, Karolos; Potrap, Igor; Potter, Christina; Potter, Christopher; Poulard, Gilbert; Poveda, Joaquin; Pozdnyakov, Valery; Pozo Astigarraga, Mikel Eukeni; Pralavorio, Pascal; Pranko, Aliaksandr; Prell, Soeren; Price, Darren; Price, Lawrence; Primavera, Margherita; Prince, Sebastien; Prokofiev, Kirill; Prokoshin, Fedor; Protopopescu, Serban; Proudfoot, James; Przybycien, Mariusz; Puddu, Daniele; Purohit, Milind; Puzo, Patrick; Qian, Jianming; Qin, Gang; Qin, Yang; Quadt, Arnulf; Quayle, William; Queitsch-Maitland, Michaela; 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Robertson, Steven; Robichaud-Veronneau, Andree; Robinson, Dave; Robinson, James; Robson, Aidan; Roda, Chiara; Rodina, Yulia; Rodriguez Perez, Andrea; Rodriguez Rodriguez, Daniel; Roe, Shaun; Rogan, Christopher Sean; Røhne, Ole; Romaniouk, Anatoli; Romano, Marino; Romano Saez, Silvestre Marino; Romero Adam, Elena; Rompotis, Nikolaos; Ronzani, Manfredi; Roos, Lydia; Ros, Eduardo; Rosati, Stefano; Rosbach, Kilian; Rose, Peyton; Rosenthal, Oliver; Rosien, Nils-Arne; Rossetti, Valerio; Rossi, Elvira; Rossi, Leonardo Paolo; Rosten, Jonatan; Rosten, Rachel; Rotaru, Marina; Roth, Itamar; Rothberg, Joseph; Rousseau, David; Royon, Christophe; Rozanov, Alexandre; Rozen, Yoram; Ruan, Xifeng; Rubbo, Francesco; Rudolph, Matthew Scott; Rühr, Frederik; Ruiz-Martinez, Aranzazu; Rurikova, Zuzana; Rusakovich, Nikolai; Ruschke, Alexander; Russell, Heather; Rutherfoord, John; Ruthmann, Nils; Ryabov, Yury; Rybar, Martin; Rybkin, Grigori; Ryu, Soo; Ryzhov, Andrey; Rzehorz, Gerhard Ferdinand; Saavedra, Aldo; 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Sawyer, Lee; Saxon, James; Sbarra, Carla; Sbrizzi, Antonio; Scanlon, Tim; Scannicchio, Diana; Scarcella, Mark; Scarfone, Valerio; Schaarschmidt, Jana; Schacht, Peter; Schachtner, Balthasar Maria; Schaefer, Douglas; Schaefer, Leigh; Schaefer, Ralph; Schaeffer, Jan; Schaepe, Steffen; Schaetzel, Sebastian; Schäfer, Uli; Schaffer, Arthur; Schaile, Dorothee; Schamberger, R Dean; Scharf, Veit; Schegelsky, Valery; Scheirich, Daniel; Schernau, Michael; Schiavi, Carlo; Schier, Sheena; Schillo, Christian; Schioppa, Marco; Schlenker, Stefan; Schmidt-Sommerfeld, Korbinian Ralf; Schmieden, Kristof; Schmitt, Christian; Schmitt, Stefan; Schmitz, Simon; Schneider, Basil; Schnoor, Ulrike; Schoeffel, Laurent; Schoening, Andre; Schoenrock, Bradley Daniel; Schopf, Elisabeth; Schott, Matthias; Schovancova, Jaroslava; Schramm, Steven; Schreyer, Manuel; Schuh, Natascha; Schulte, Alexandra; Schultens, Martin Johannes; Schultz-Coulon, Hans-Christian; Schulz, Holger; Schumacher, Markus; Schumm, Bruce; Schune, Philippe; Schwartzman, Ariel; Schwarz, Thomas Andrew; Schweiger, Hansdieter; Schwemling, Philippe; Schwienhorst, Reinhard; Schwindling, Jerome; Schwindt, Thomas; Sciolla, Gabriella; Scuri, Fabrizio; Scutti, Federico; Searcy, Jacob; Seema, Pienpen; Seidel, Sally; Seiden, Abraham; Seifert, Frank; Seixas, José; Sekhniaidze, Givi; Sekhon, Karishma; Sekula, Stephen; Seliverstov, Dmitry; Semprini-Cesari, Nicola; Serfon, Cedric; Serin, Laurent; Serkin, Leonid; Sessa, Marco; Seuster, Rolf; Severini, Horst; Sfiligoj, Tina; Sforza, Federico; Sfyrla, Anna; Shabalina, Elizaveta; Shaikh, Nabila Wahab; Shan, Lianyou; Shang, Ruo-yu; Shank, James; Shapiro, Marjorie; Shatalov, Pavel; Shaw, Kate; Shaw, Savanna Marie; Shcherbakova, Anna; Shehu, Ciwake Yusufu; Sherwood, Peter; Shi, Liaoshan; Shimizu, Shima; Shimmin, Chase Owen; Shimojima, Makoto; Shiyakova, Mariya; Shmeleva, Alevtina; Shoaleh Saadi, Diane; Shochet, Mel; Shojaii, Seyed Ruhollah; Shrestha, Suyog; Shulga, Evgeny; Shupe, Michael; Sicho, Petr; Sickles, Anne Marie; Sidebo, Per Edvin; Sidiropoulou, Ourania; Sidorov, Dmitri; Sidoti, Antonio; Siegert, Frank; Sijacki, Djordje; Silva, José; Silverstein, Samuel; Simak, Vladislav; Simic, Ljiljana; Simion, Stefan; Simioni, Eduard; Simmons, Brinick; Simon, Dorian; Simon, Manuel; Sinervo, Pekka; Sinev, Nikolai; Sioli, Maximiliano; Siragusa, Giovanni; Sivoklokov, Serguei; Sjölin, Jörgen; Skinner, Malcolm Bruce; Skottowe, Hugh Philip; Skubic, Patrick; Slater, Mark; Slavicek, Tomas; Slawinska, Magdalena; Sliwa, Krzysztof; Slovak, Radim; Smakhtin, Vladimir; Smart, Ben; Smestad, Lillian; Smiesko, Juraj; Smirnov, Sergei; Smirnov, Yury; Smirnova, Lidia; Smirnova, Oxana; Smith, Matthew; Smith, Russell; Smizanska, Maria; Smolek, Karel; Snesarev, Andrei; Snyder, Scott; Sobie, Randall; Socher, Felix; Soffer, Abner; Soh, Dart-yin; Sokhrannyi, Grygorii; Solans Sanchez, Carlos; Solar, Michael; Soldatov, Evgeny; Soldevila, Urmila; Solodkov, Alexander; Soloshenko, Alexei; Solovyanov, Oleg; Solovyev, Victor; Sommer, Philip; Son, Hyungsuk; Song, Hong Ye; Sood, Alexander; Sopczak, Andre; Sopko, Vit; Sorin, Veronica; Sosa, David; Sotiropoulou, Calliope Louisa; Soualah, Rachik; Soukharev, Andrey; South, David; Sowden, Benjamin; Spagnolo, Stefania; Spalla, Margherita; Spangenberg, Martin; Spanò, Francesco; Sperlich, Dennis; Spettel, Fabian; Spighi, Roberto; Spigo, Giancarlo; Spiller, Laurence Anthony; Spousta, Martin; St Denis, Richard Dante; Stabile, Alberto; Stamen, Rainer; Stamm, Soren; Stanecka, Ewa; Stanek, Robert; Stanescu, Cristian; Stanescu-Bellu, Madalina; Stanitzki, Marcel Michael; Stapnes, Steinar; Starchenko, Evgeny; Stark, Giordon; Stark, Jan; Staroba, Pavel; Starovoitov, Pavel; Stärz, Steffen; Staszewski, Rafal; Steinberg, Peter; Stelzer, Bernd; Stelzer, Harald Joerg; Stelzer-Chilton, Oliver; Stenzel, Hasko; Stewart, Graeme; Stillings, Jan Andre; Stockton, Mark; Stoebe, Michael; Stoicea, Gabriel; Stolte, Philipp; Stonjek, Stefan; Stradling, Alden; Straessner, Arno; Stramaglia, Maria Elena; Strandberg, Jonas; Strandberg, Sara; Strandlie, Are; Strauss, Michael; Strizenec, Pavol; Ströhmer, Raimund; Strom, David; Stroynowski, Ryszard; Strubig, Antonia; Stucci, Stefania Antonia; Stugu, Bjarne; Styles, Nicholas Adam; Su, Dong; Su, Jun; Suchek, Stanislav; Sugaya, Yorihito; Suk, Michal; Sulin, Vladimir; Sultansoy, Saleh; Sumida, Toshi; Sun, Siyuan; Sun, Xiaohu; Sundermann, Jan Erik; Suruliz, Kerim; Susinno, Giancarlo; Sutton, Mark; Suzuki, Shota; Svatos, Michal; Swiatlowski, Maximilian; Sykora, Ivan; Sykora, Tomas; Ta, Duc; Taccini, Cecilia; Tackmann, Kerstin; Taenzer, Joe; Taffard, Anyes; Tafirout, Reda; Taiblum, Nimrod; Takai, Helio; Takashima, Ryuichi; Takeshita, Tohru; Takubo, Yosuke; Talby, Mossadek; Talyshev, Alexey; Tan, Kong Guan; Tanaka, Junichi; Tanaka, Masahiro; Tanaka, Reisaburo; Tanaka, Shuji; Tannenwald, Benjamin Bordy; Tapia Araya, Sebastian; Tapprogge, Stefan; Tarem, Shlomit; Tartarelli, Giuseppe Francesco; Tas, Petr; Tasevsky, Marek; Tashiro, Takuya; Tassi, Enrico; Tavares Delgado, Ademar; Tayalati, Yahya; Taylor, Aaron; Taylor, Geoffrey; Taylor, Pierre Thor Elliot; Taylor, Wendy; Teischinger, Florian Alfred; Teixeira-Dias, Pedro; Temming, Kim Katrin; Temple, Darren; Ten Kate, Herman; Teng, Ping-Kun; Teoh, Jia Jian; Tepel, Fabian-Phillipp; Terada, Susumu; Terashi, Koji; Terron, Juan; Terzo, Stefano; Testa, Marianna; Teuscher, Richard; Theveneaux-Pelzer, Timothée; Thomas, Juergen; Thomas-Wilsker, Joshuha; Thompson, Emily; Thompson, Paul; Thompson, Stan; Thomsen, Lotte Ansgaard; Thomson, Evelyn; Thomson, Mark; Tibbetts, Mark James; Ticse Torres, Royer Edson; Tikhomirov, Vladimir; Tikhonov, Yury; Timoshenko, Sergey; Tipton, Paul; Tisserant, Sylvain; Todome, Kazuki; Todorov, Theodore; Todorova-Nova, Sharka; Tojo, Junji; Tokár, Stanislav; Tokushuku, Katsuo; Tolley, Emma; Tomlinson, Lee; Tomoto, Makoto; Tompkins, Lauren; Toms, Konstantin; Tong, Baojia(Tony); Torrence, Eric; Torres, Heberth; Torró Pastor, Emma; Toth, Jozsef; Touchard, Francois; Tovey, Daniel; Trefzger, Thomas; 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Valderanis, Chrysostomos; Valdes Santurio, Eduardo; Valencic, Nika; Valentinetti, Sara; Valero, Alberto; Valery, Loic; Valkar, Stefan; Valls Ferrer, Juan Antonio; Van Den Wollenberg, Wouter; Van Der Deijl, Pieter; van der Graaf, Harry; van Eldik, Niels; van Gemmeren, Peter; Van Nieuwkoop, Jacobus; van Vulpen, Ivo; van Woerden, Marius Cornelis; Vanadia, Marco; Vandelli, Wainer; Vanguri, Rami; Vaniachine, Alexandre; Vankov, Peter; Vardanyan, Gagik; Vari, Riccardo; Varnes, Erich; Varol, Tulin; Varouchas, Dimitris; Vartapetian, Armen; Varvell, Kevin; Vasquez, Jared Gregory; Vazeille, Francois; Vazquez Schroeder, Tamara; Veatch, Jason; Veeraraghavan, Venkatesh; Veloce, Laurelle Maria; Veloso, Filipe; Veneziano, Stefano; Ventura, Andrea; Venturi, Manuela; Venturi, Nicola; Venturini, Alessio; Vercesi, Valerio; Verducci, Monica; Verkerke, Wouter; Vermeulen, Jos; Vest, Anja; Vetterli, Michel; Viazlo, Oleksandr; Vichou, Irene; Vickey, Trevor; Vickey Boeriu, Oana Elena; Viehhauser, Georg; Viel, Simon; 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Watts, Gordon; Watts, Stephen; Waugh, Ben; Webb, Samuel; Weber, Michele; Weber, Stefan Wolf; Webster, Jordan S; Weidberg, Anthony; Weinert, Benjamin; Weingarten, Jens; Weiser, Christian; Weits, Hartger; Wells, Phillippa; Wenaus, Torre; Wengler, Thorsten; Wenig, Siegfried; Wermes, Norbert; Werner, Matthias; Werner, Michael David; Werner, Per; Wessels, Martin; Wetter, Jeffrey; Whalen, Kathleen; Whallon, Nikola Lazar; Wharton, Andrew Mark; White, Andrew; White, Martin; White, Ryan; Whiteson, Daniel; Wickens, Fred; Wiedenmann, Werner; Wielers, Monika; Wienemann, Peter; Wiglesworth, Craig; Wiik-Fuchs, Liv Antje Mari; Wildauer, Andreas; Wilk, Fabian; Wilkens, Henric George; Williams, Hugh; Williams, Sarah; Willis, Christopher; Willocq, Stephane; Wilson, John; Wingerter-Seez, Isabelle; Winklmeier, Frank; Winston, Oliver James; Winter, Benedict Tobias; Wittgen, Matthias; Wittkowski, Josephine; Wolf, Tim Michael Heinz; Wolter, Marcin Wladyslaw; Wolters, Helmut; Worm, Steven D; Wosiek, Barbara; Wotschack, Jorg; Woudstra, Martin; Wozniak, Krzysztof; Wu, Mengqing; Wu, Miles; Wu, Sau Lan; Wu, Xin; Wu, Yusheng; Wyatt, Terry Richard; Wynne, Benjamin; Xella, Stefania; Xu, Da; Xu, Lailin; Yabsley, Bruce; Yacoob, Sahal; Yamaguchi, Daiki; Yamaguchi, Yohei; Yamamoto, Akira; Yamamoto, Shimpei; Yamanaka, Takashi; Yamauchi, Katsuya; Yamazaki, Yuji; Yan, Zhen; Yang, Haijun; Yang, Hongtao; Yang, Yi; Yang, Zongchang; Yao, Weiming; Yap, Yee Chinn; Yasu, Yoshiji; Yatsenko, Elena; Yau Wong, Kaven Henry; Ye, Jingbo; Ye, Shuwei; Yeletskikh, Ivan; Yen, Andy L; Yildirim, Eda; Yorita, Kohei; Yoshida, Rikutaro; Yoshihara, Keisuke; Young, Charles; Young, Christopher John; Youssef, Saul; Yu, David Ren-Hwa; Yu, Jaehoon; Yu, Jiaming; Yu, Jie; Yuan, Li; Yuen, Stephanie P; Yusuff, Imran; Zabinski, Bartlomiej; Zaidan, Remi; Zaitsev, Alexander; Zakharchuk, Nataliia; Zalieckas, Justas; Zaman, Aungshuman; Zambito, Stefano; Zanello, Lucia; Zanzi, Daniele; Zeitnitz, Christian; Zeman, Martin; Zemla, Andrzej; Zeng, Jian Cong; Zeng, Qi; Zengel, Keith; Zenin, Oleg; Ženiš, Tibor; Zerwas, Dirk; Zhang, Dongliang; Zhang, Fangzhou; Zhang, Guangyi; Zhang, Huijun; Zhang, Jinlong; Zhang, Lei; Zhang, Rui; Zhang, Ruiqi; Zhang, Xueyao; Zhang, Zhiqing; Zhao, Xiandong; Zhao, Yongke; Zhao, Zhengguo; Zhemchugov, Alexey; Zhong, Jiahang; Zhou, Bing; Zhou, Chen; Zhou, Lei; Zhou, Li; Zhou, Mingliang; Zhou, Ning; Zhu, Cheng Guang; Zhu, Hongbo; Zhu, Junjie; Zhu, Yingchun; Zhuang, Xuai; Zhukov, Konstantin; Zibell, Andre; Zieminska, Daria; Zimine, Nikolai; Zimmermann, Christoph; Zimmermann, Stephanie; Zinonos, Zinonas; Zinser, Markus; Ziolkowski, Michael; Živković, Lidija; Zobernig, Georg; Zoccoli, Antonio; zur Nedden, Martin; Zwalinski, Lukasz

    2016-08-31

    Searches for exclusively produced $W$ boson pairs in the process $pp(\\gamma\\gamma) \\rightarrow pW^+W^-p$ and exclusively produced Higgs boson in the process $pp(gg) \\rightarrow pHp$ have been performed using $e^{\\pm}\\mu^{\\mp}$ final states. These measurements use 20.2 fb$^{-1}$ of $pp$ collisions collected by the ATLAS experiment at a center-of-mass energy $\\sqrt{s}=8$ TeV at the LHC. Exclusive production of $W^+W^-$ consistent with the Standard Model prediction is found with 3.0$\\sigma$ significance. The exclusive $W^+W^-$ production cross-section is determined to be $\\sigma (\\gamma\\gamma\\rightarrow W^{+}W^{-}\\rightarrow e^{\\pm}\\mu^{\\mp} X) = 6.9 \\pm 2.2 (\\mathrm{stat.}) \\pm 1.4 (\\mathrm{sys.})$ fb, in agreement with the Standard Model prediction. Limits on anomalous quartic gauge couplings are set at 95\\% confidence-level as $-1.7 \\times 10^{-6} < a_0^W/\\Lambda^2 < 1.7 \\times 10^{-6}$ GeV$^{-2}$and $-6.4 \\times 10^{-6} < a_C^W/\\Lambda^2 < 6.3 \\times 10^{-6}$ GeV$^{-2}$. A 95\\% confidence-level u...

  4. Local Conduction in Mo xW1- xSe2: The Role of Stacking Faults, Defects, and Alloying.

    Science.gov (United States)

    Bampoulis, Pantelis; Sotthewes, Kai; Siekman, Martin H; Zandvliet, Harold J W

    2018-04-18

    Here, we report on the surface conductivity of WSe 2 and Mo x W 1- x Se 2 (0 ≤ x ≤ 1) crystals investigated with conductive atomic force microscopy. We found that stacking faults, defects, and chemical heterogeneities form distinct two-dimensional and one-dimensional conduction paths on the transition metal dichalcogenide surface. In the case of WSe 2 , in addition to step edges, we find a significant amount of stacking faults (formed during the cleaving process) that strongly influence the surface conductivity. These regions are attributed to the alternation of the 2H and 3R polytypism. The stacking faults form regular 2D patterns by alternation of the underlying stacking order, with a periodicity that varies significantly between different regions and samples. In the case of Mo x W 1- x Se 2 , its conductivity has a localized nature, which depends on the underlying chemical composition and the Mo/W ratio. Segregation to W-rich and Mo-rich regions during the growth process leads to nonuniform conduction paths on the surface of the alloy. We found a gradual change of the conductivity moving from one region to the other, reminiscent of lateral band bending. Our results demonstrate the use of C-AFM as a nanoscopic tool to probe the electrical properties of largely inhomogeneous samples and show the complicated nature of the surface conductivity of TMDC alloys.

  5. Measurements of W{sup ±} and top-quark pair to Z-boson cross-section ratios at √(s)=13,8,7 TeV with the ATLAS detector

    Energy Technology Data Exchange (ETDEWEB)

    Trofymov, Artur

    2018-01-15

    Measurements of the Z→l{sup +}l{sup -} production cross sections, where l{sup ±}=e{sup ±},μ{sup ±}, in proton-proton collisions at √(s)=13 TeV are presented using two sets of data recorded by the ATLAS experiment at the Large Hadron Collider. The data sets correspond to a total integrated luminosity of 81 pb{sup -1} and 3.2 fb{sup -1} collected in 2015 using the 50 ns and 25 ns bunch spacing configurations, respectively. The cross section obtained with 50 ns configuration is used for W{sup ±} to Z cross-section ratio measurement. The W{sup +} to W{sup -} boson production cross-section ratio is also measured. The ratios of measured fiducial cross sections for electron and muon decay channels of the W{sup ±} and Z boson are evaluated and compared to the Standard Model expectations of the lepton universality. Ratio of top-quark pair to Z-boson production cross section is measured at √(s)=13 TeV using 25 ns bunch spacing data. Similar ratios are obtained at √(s)=8 TeV and 7 TeV using the published ATLAS results corrected to a common phase space. Single ratios, at a given √(s) for the two processes and at different √(s) for each process, as well as double ratios of the two processes at different √(s), are evaluated. The results are compared to calculations performed at next-to-next-to-leading-order accuracy using recent sets of parton distribution functions. The data used for t anti t to Z-boson cross section ratios demonstrate significant power to constrain the gluon distribution function for the Bjorken-x values near 0.1 and the light-quark sea for x<0.02.

  6. Neutron-activation analysis of phosphorus in aluminium-silicon alloys

    International Nuclear Information System (INIS)

    Rajchev, Kh.

    1976-01-01

    Silicon-aluminium alloy samples weighing about 50 mg are irradiated in a nuclear reactor with a neutron flow of 5x10 12 neutrons, cm -2 .s -1 . After a period of one week for decay of the short-lived isotopes, the sample is dissolved in a mixture of nitric and hydrofluoric acid. It is neutralized up to pH 2,5 and the present radioactive two- and three-valent cations are sorbed on chelating ion exchange resin Dowex A1. An ammonium phosphate standard is irradiated in parallel with the sample for qualitative determinations. The quantity of phosphorus is measured in aliquots from the sample and the standard with a liquid counter. The method proposed for separating and determining the phosphorus in silumins ensures practically the full separation of phosphorus (98,5 +- 0,5 %) and a precise determination of microquantities of the element - up to 10 -10 g. (author)

  7. Interfacial hydrothermal synthesis of nanorod-like CdMo{sub 1−x}W{sub x}O{sub 4} solid solutions with enhanced photocatalytic performance

    Energy Technology Data Exchange (ETDEWEB)

    Hou, Linrui, E-mail: houlr629@163.com; Lian, Lin; Zhang, Longhai; Zhou, Lu; Yuan, Changzhou, E-mail: ayuancz@163.com

    2014-12-15

    In the work, CdMo{sub 1−x}W{sub x}O{sub 4} solid solutions with various compositions in the entire range of 0 ≤ x ≤ 1 have been prepared successfully by a facile interfacial hydrothermal method. All CdMo{sub 1−x}W{sub x}O{sub 4} products are composed of one-dimensional (1D) nanorods (NRs) with tetragonal structure. The composition-dependent structure, absorption properties and photocatalytic efficiencies of the resulting 1D CdMo{sub 1−x}W{sub x}O{sub 4} samples are systematically investigated. The photocatalytic degradation of methylene blue (MB) under ultraviolet (UV) light irradiation was utilized as a model reaction to evaluate the photocatalytic activities of all the samples. The sample, CdMo{sub 0.5}W{sub 0.5}O{sub 4} (i.e., x = 0.5) NRs, exhibits the highest photocatalytic activity and appealing stability for widespread photocatalytic application, owing to the unique 1D nanoscale architecture, suitable band gap and strong absorption in the UV region. Our approach developed here provides an elegant technique to tune both the nanoarchitecture and band gap of the photocatalysts by simply adjusting the composition of the solid solutions, resulting in the enhanced photocatalytic activity. Moreover, the method we proposed can be further extended to the smart design and controllable synthesis of other novel and highly efficient multi-component photocatalysts for environmental remediation. - Graphical abstract: 1D nanorod-based CdMo{sub 1−x}W{sub x}O{sub 4} solid solutions with various W compositions in the entire range of 0 ≤ x ≤ 1 were fabricated by a facile interfacial hydrothermal strategy, and exhibited intriguing photodecomposition of the MB under UV light irradiation. - Highlights: • CdMo{sub 1−x}W{sub x}O{sub 4} solid solutions with W compositions of 0 ≤ x ≤ 1 were prepared. • Facile interfacial hydrothermal strategy was developed. • 1D nanorod-based CdMo{sub 1−x}W{sub x}O{sub 4} photocatalysts were synthesized.

  8. Measurement of core plasma temperature and rotation on W7-X made available by the x-ray imaging crystal spectrometer (XICS)

    Energy Technology Data Exchange (ETDEWEB)

    Pablant, N A; Bitter, M; Burhenn, R; Delgado-Aparicio, L; Ellis, R; Gates, D; Goto, M; Hill, K W; Langenberg, A; Lazerson, S; Mardenfeld, M; Morita, S; Neilson, G H; Oishi, T; Pedersen, T S

    2014-07-01

    A new x-ray imaging crystal spectrometer diagnostic (XICS) is currently being built for installation on W7-X. This diagnostic will contribute to the study of ion and electron thermal transport and the evolution of the radial electric field by providing high resolution temperature and rotation measurements under many plasma conditions, including ECH heated plasmas. Installation is expected before the first experimental campaign (OP1.1), making an important set of measurements available for the first W7-X plasmas. This diagnostic will also work in concert with the HR-XCS diagnostic to provide an excellent diagnostic set for core impurity transport on W7-X.

  9. Results of the examinations of the W7-X pre-series target elements

    International Nuclear Information System (INIS)

    Boscary, J.; Boeswirth, B.; Greuner, H.; Streibl, B.; Missirlian, M.; Schlosser, J.; Schedler, B.; Scheiber, K.

    2006-01-01

    The highly heat-loaded area of the target plates of the WENDELSTEIN 7-X (W7-X) divertor is formed by 890 water-cooled target elements (TEs). This surface is designed to sustain a maximum stationary heat flux of 10 MW/m 2 and to remove a maximum power of 100 kW per element. Flat tiles made of CFC Sepcarb(r) NB31 are bonded to a CuCrZr heat sink. This joint is manufactured in two stages. In the first step, an OFHC copper interlayer is cast onto the tile by active metal casting (AMC(r)). At this stage, the joint copper-CFC is inspected by X-ray and lock-in thermography. In the second step, the AMC(r)-NB31 tiles are joined to CuCrZr. Two technologies have been investigated: electron beam welding (EBW) and hot isostatic pressing (HIP). The joint copper-CuCrZr is examined by ultrasonic method. At the end of the fabrication, the bond between the heat sink and the CFC tiles is inspected by thermography methods. The produced CFC NB31 material for W7-X showed a large scatter in the tensile strength in the ex-pitch direction in the range of 50 - 110 MPa. Pre-series TEs have been manufactured to qualify the design, the fabrication, the relevant non-destructive examinations (NDEs) and the delivered CFC for the serial production. The whole manufacturing route is validated if the delivered elements withstand operating conditions similar to those in W7-X in the high heat flux (HHF) test facility GLADIS without degradation of performance and integrity. HHF tests did not show any effect that could be attributed to the CFC grade or to the joining method. The HHF test results exhibited a high percentage of defective tiles, indicated by hot spots at the border of the CFC surface. Visual inspections after HHF tests have mostly correlated these spots to the initiation and /or propagation of cracks at the lateral edge of the tiles in CFC at the interface CFC-copper. The pre-series activities have been extended to reduce the stresses at the critical AMC(r) interface. By means of

  10. Evaluation of degree of conversion and the effect of thermal aging on the color stability of resin cements and flowable composite.

    Science.gov (United States)

    Prieto, Lúcia Trazzi; Pimenta de Araújo, Cíntia Tereza; Araujo Pierote, Josué Junior; Salles de Oliveira, Dayane Carvalho Ramos; Coppini, Erick Kamiya; Sartini Paulillo, Luís Alexandre Maffei

    2018-01-01

    The aim of this in vitro study was to evaluate the color stability and degree of conversion (DC) of dual-cure and light-cure cements and flowable composites after thermal aging. A total of 50 human incisors were prepared and divided into six groups ( n = 10). Veneers were fabricated using IPS Empress Direct composite resin were bonded with three types of luting agents: Light-cured, conventional dual, and flowable composite according to the manufacturer's instructions. The groups were as follows: Filtek Z350XT Flow/Single Bond 2, RelyX ARC/Single Bond 2, RelyX Veneer/Single Bond 2, Tetric N-Flow/Tetric N-Bond, and Variolink II/Tetric N-Bond. Commission Internationale de l'Éclairage L*, a* and b* color coordinates were measured 24 h after cementation procedure with a color spectrophotometer and reevaluated after 10,000 thermal cycles. To evaluate the DC 50 specimens ( n = 10) of each resin material were obtained and Fourier transform infrared spectroscopy was used to evaluate the absorption spectra. Statistical analysis was performed with one-way ANOVA and Tukey's test (α = 0.05). No statistically significant differences in ΔE* occurred after aging. The greatest change in lightness occurred in the Variolink II resin cement. Changes in red-green hue were very small for the same cement and largest in the Tetric N-Flow flowable resin composite, while the greatest change in blue-yellow hue was a yellowing of the RelyX ARC luting cement. RelyX ARC exhibited the highest DC, and there were no statistically significant differences in DC among the other cements. Resin-based luting agent might affect the final of ceramic veneer restorations. The thermal aging affected the final color of the evaluated materials, and these were regarded as clinically unacceptable (ΔE >3.3).

  11. Database structures and interfaces for W7-X

    International Nuclear Information System (INIS)

    Heimann, P.; Bluhm, T.; Hennig, Ch.; Kroiss, H.; Kuehner, G.; Maier, J.; Riemann, H.; Zilker, M.

    2008-01-01

    The W7-X experiment of the IPP, under construction in Greifswald Germany, is designed to operate in a quasi-steady-state scenario. The database structures and interfaces used for discharge description and execution have to reflect this continuous mode of operation. In close collaboration between the control group of W7-X and the data acquisition group a combined design of the data structures used for describing the configuration and the operation of the experiment was developed. To guarantee access to this information from all participating stations a TCP/IP portal and a proxy server were developed. This portal enables especially the VxWorks real-time operating systems of the control stations to access the information in the object-oriented database. The database schema includes now a more functional description of the experiment and gives the physicists a more simplified view of the necessary definitions of operational parameters. The scheduling of the long discharges of W7-X will be done by predefining operational parameters in segments and scenarios, where a scenario is a fixed sequence of segments with a common physical background. To hide the specialized information contained in the basic parameters from the experiment leader or physicist an abstraction layer was introduced that only shows physically interesting information. An executable segment will be generated after verifying the consistency of the high-level parameters by using a transformation function for every basic parameter needed. Since the database contains all configurations and discharge definitions necessary to operate the experiment, it is very important to give the user a tool to manipulate this information in an intuitive way. A special editor (ConfiX) was designed and implemented for this task. At the moment the basic functionality for dealing with all kind of objects in the database is available. Future releases will extend the functionality to defining and editing configurations, segments

  12. Bulk-Fill Resin Composites

    DEFF Research Database (Denmark)

    Benetti, Ana Raquel; Havndrup-Pedersen, Cæcilie; Honoré, Daniel

    2015-01-01

    the restorative procedure. The aim of this study, therefore, was to compare the depth of cure, polymerization contraction, and gap formation in bulk-fill resin composites with those of a conventional resin composite. To achieve this, the depth of cure was assessed in accordance with the International Organization...... for Standardization 4049 standard, and the polymerization contraction was determined using the bonded-disc method. The gap formation was measured at the dentin margin of Class II cavities. Five bulk-fill resin composites were investigated: two high-viscosity (Tetric EvoCeram Bulk Fill, SonicFill) and three low......-viscosity (x-tra base, Venus Bulk Fill, SDR) materials. Compared with the conventional resin composite, the high-viscosity bulk-fill materials exhibited only a small increase (but significant for Tetric EvoCeram Bulk Fill) in depth of cure and polymerization contraction, whereas the low-viscosity bulk...

  13. Analysis of gap formation at tooth-composite resin interface: effect of C-factor and light-curing protocol

    Directory of Open Access Journals (Sweden)

    Gustavo Oliveira dos Santos

    2007-08-01

    Full Text Available OBJECTIVE: The aim of this study was to evaluate the effect of C-factor and light-curing protocol on gap formation in composite resin restorations. Material and METHODS: Cylindrical cavities with 5.0 mm diameter and three different depths (A=1.0, B=2.0 and C=3.0 mm were prepared on the occlusal surface of 30 human molars and restored in a single increment with P 60. The composite resin was light-cured according to two protocols: standard - 850 mW/cm² / 20 s and gradual - 100 up to 1000 mW/cm² / 10 s + 1000 mW/cm² / 10 s. After storage in distilled water (37°C/7 days, the restorations were cut into three slices in a buccolingual direction and the gap widths were analyzed using a 3D-scanning system. The data were submitted to ANOVA and Student-Newman-Keuls test (alpha=0.05. RESULTS: ANOVA detected a significant influence for the C-factor and light-curing protocol as independent factors, and for the double interaction C-factor vs. light-curing protocol. Cavities with higher C-factor presented the highest gap formation. The gradual light-curing protocol led to smaller gap formation at cavity interfaces. CONCLUSIONS: The findings of this study suggest that the C-factor played an essential role in gap formation. The gradual light-curing protocol may allow relaxation of composite resin restoration during polymerization reaction.

  14. 50 kW laser weapon demonstrator of Rheinmetall Waffe munition

    Science.gov (United States)

    Ludewigt, K.; Riesbeck, Th.; Graf, A.; Jung, M.

    2013-10-01

    We will present the setup of a 50 kW Laser Weapon Demonstrator (LWD) and results achieved with this system. The LWD is a ground based Air Defence system consisting of a Skyguard sensor unit for target acquisition and two laser equipped weapon turrets. The weapon turrets used are standard air defence turrets of Rheinmetall Air Defence which were equipped with several 10 kW Laser Weapon Modules (LWM). Each LWM consists of one 10 kW fiber laser and a beam forming unit (BFU). Commercial of the shelf fiber laser were modified for our defence applications. The BFU providing diffraction limited beam focusing, target imaging and fine tracking of the target was developed. The LWD was tested in a firing campaign at Rheinmetall test ground in Switzerland. All laser beams of both weapon turrets were superimposed on stationary and dynamic targets. Test results of the LWD for the scenarios Air Defence and C-RAMM (counter rockets, artillery, mortar and missiles) will be presented. An outlook for the next development stage towards a 100 kW class laser weapon on RWM will be given.

  15. [Study on color of thermosetting resin for veneer crown].

    Science.gov (United States)

    Kamitomai, H

    1989-02-01

    Based on the viewpoint that stresses the importance of achieving natural colors and forms for veneer crown, four representative kinds of thermosetting resins were investigated colorimetrically in an attempt to clarify the relationship between the thickness and color of resins in opaque, dentin and enamel colors respectively. A spectrophotometer was used to measure the colors, the CIE colorimetric system employed to show the readings, and the CIE 1964 U*V*W* space was utilized to indicate the color differences, with the following results. 1. In the case of dentin, certain specific colors were observed for thickness of 1.3 to 1.8 mm when used alone, but when applied over opaque the range was 0.2 to 0.5 mm lower than when used alone. 2. Enamel resins were grouped into two types according to different color groups, one group similar to achromatic color with low limpidity and the other similar to the dentin color with high limpidity. The former type became more grayer with an increase in thickness when applied over dentin. The latter type showed no difference in color even when the thickness increased. This study has shown that the facing color results vary depending on the color properties of the different resins used. Therefore, it is advisable that careful consideration be given to these differencies in order to achieve the intended color facing.

  16. First principles study of structural stability and site preference in Co3 (W,X

    Directory of Open Access Journals (Sweden)

    Joshi Sri Raghunath

    2014-01-01

    Full Text Available Since the discovery [1] of γ′ precipitate (L12 – Co3(Al, W in the Co-Al-W ternary system, there has been an increased interest in Co-based superalloys. Since these alloys have two phase microstructures (γ + γ′ similar to Ni-based superalloys [2], they are viable candidates in high temperature applications, particularly in land-based turbines. The role of alloying on stability of the γ′ phase has been an active area of research. In this study, electronic structure calculations were done to probe the effect of alloying in Co3W with L12 structure. Compositions of type Co3(W,X, (where X/Y = Mn, Fe, Ni, Pt, Cr , Al, Si, V, W, Ta, Ti, Nb, Hf, Zr and Mo were studied. Effect of alloying on equilibrium lattice parameters and ground state energies was used to calculate Vegard's coefficients and site preference related data. The effect of alloying on the stability of the L12 structure vis a vis other geometrically close packed ordered structures was also studied for a range of Co3X compounds. Results suggest that the penchant of element for the W sublattice can be predicted by comparing heats of formation of Co3X in different structures.

  17. Bituminous solidification, disposal, transport and burial of spent ion-exchange resins. Part of a coordinated programme on treatment of spent ion exchange resins

    International Nuclear Information System (INIS)

    Mozes, G.; Kristof, M.

    1983-07-01

    The project dealing with the incorporation of spent ion-exchange resins into bitumen was performed within the Agency coordinated research programme on treatment of spent ion-exchange resins. Physical and chemical properties of commercial ion-exchange resins, bitumens and bituminized resins were studied. It was shown that bitumen with low oil content and with a softening point of 60-70 deg. C are applicable for the incorporation of resins. The final waste form is allowed to contain maximum 50% resin. The comprehensive study of the biological resistance of B-30 bitumen was performed. That showed that any bacteriological attack can be regarded as generally insignificant. A continuously operating technology was realized on a semi-plant scale. The best operating conditions of this technology were determined. On the basis of the experience gained from the experiments a design of the bituminization plant of 50m 3 dry resin/year treatment capacity was proposed

  18. [Studies on the process of Herba Clinopodii saponins purified with macroporous adsorption resin].

    Science.gov (United States)

    Zhang, Yi; Yan, Dan; Han, Yumei

    2005-10-01

    To study the technological parameters of the purification process of saponins with macroporous adsorption resin. The adsorptive characteristics and elutive parameters of the process were studied by taking the elutive and purified ratio of saponins as markers. 11.4 ml of the extraction of Herba Clinopodii (crude drugs 0.2 g/ml) was purified with a column of macroporous adsorption resin (phi15 mm x H90 mm, dry weight 2.5 g) and washed with 3BV of distilled water, then eluted with 3BV of 30% ethanol and 3BV of 70% ethanol. Most of saponins were collected in the 70% ethanol. With macroporous adsorption resin adsorbing and purifying,the elutive ratio of saponins is 86.8% and the purity reaches 153.2%. So this process of applying macroporous adsorption resin to adsorb and purify Saponins is feasible.

  19. Application conditions for ester cured alkaline phenolic resin sand

    Directory of Open Access Journals (Sweden)

    Ren-he Huang

    2016-07-01

    Full Text Available Five organic esters with different curing speeds: propylene carbonate (i.e. high-speed ester A; 1, 4-butyrolactone; glycerol triacetate (i.e. medium-speed ester B; glycerol diacetate; dibasic ester (DBE (i.e. low-speed ester C, were chosen to react with alkaline phenolic resin to analyze the application conditions of ester cured alkaline phenolic resin. The relationships between the curing performances of the resin (including pH value, gel pH value, gel time of resin solution, heat release rate of the curing reaction and tensile strength of the resin sand and the amount of added organic ester and curing temperature were investigated. The results indicated the following: (1 The optimal added amount of organic ester should be 25wt.%-30wt.% of alkaline phenolic resin and it must be above 20wt.%-50 wt.% of the organic ester hydrolysis amount. (2 High-speed ester A (propylene carbonate has a higher curing speed than 1, 4-butyrolactone, and they were both used as high-speed esters. Glycerol diacetate is not a high-speed ester in alkaline phenolic resin although it was used as a high-speed ester in ester cured sodium silicate sand; glycerol diacetate and glycerol triacetate can be used as medium-speed esters in alkaline phenolic resin. (3 High-speed ester A, medium-speed ester B (glycerol triacetate and low-speed ester C (dibasic ester, i.e., DBE should be used below 15 ìC, 35 ìC and 50 ìC, respectively. High-speed ester A or low-speed ester C should not be used alone but mixed with medium-speed ester B to improve the strength of the resin sand. (4 There should be a suitable solid content (generally 45wt.%-65wt.% of resin, alkali content (generally 10wt.%-15wt.% of resin and viscosity of alkaline phenolic resin (generally 50-300 mPa≤s in the preparation of alkaline phenolic resin. Finally, the technique conditions of alkaline phenolic resin preparation and the application principles of organic ester were discussed.

  20. Application of Resin in Pulp Technique for Ion Exchange Separation of Uranium from Alkaline Leachate

    International Nuclear Information System (INIS)

    Sreenivas, T.; Rajan, K.C.; Chakravartty, J.K.

    2014-01-01

    Conclusions: • Resin-in-pulp technique was applied for purification and enrichment of uranium values from a finely ground uranium ore leach slurry of alkaline nature using strong base anion exchange resin (size 500 - 675μm). • The chemical composition of the solution phase of the alkaline leach slurry (pH 9.5) was consisting of about 40 g/L of total dissolved solutes (TDS) predominantly with Na_2CO_3 and NaHCO_3 and minor levels of Na_2SO_4. The uranium content was only 730 mg/L and d50 of solids was 34μm. • Amongst the various commercially available resins studied PFA 4740 and 4783 having quaternary ammonium ion on polystyrene crosslink with divibyl benzez (DVB) gave best performance. The maximum loading capacity achieved in the RIP studies was about 60-65 g of U_3O_8/L of wet settled resin amounting to 98% of loading. This has necessitated 4 stages of counter-current extraction with overall contact time of 100 minutes at a resin to leach slurry volume ratio of about 1:50. Practically the entire uranium values loaded on the resin were eluted using NaCl. • The RIP process was found quite efficient for uranium bearing alkaline leach slurries.

  1. Analysis of surface hardness of artificially aged resin composites

    Directory of Open Access Journals (Sweden)

    Denise Cremonezzi Tornavoi

    2012-02-01

    Full Text Available This study evaluated the effect of artificially accelerated aging (AAA on the surface hardness of eight composite resins: Filtek Z250, Filtek Supreme, 4 Seasons, Herculite, P60, Tetric Ceram, Charisma, and Filtek Z100. Sixteen specimens were made from the test piece of each material, using an 8.0 × 2.0 mm teflon matrix. After 24 hours, eight specimens from each material were submitted to three surface hardness readings using a Shimadzu Microhardness Tester for 5 seconds at a load of 50 gf. The other eight specimens remained in the artificially accelerated aging machine for 382 hours and were submitted to the same surface hardness analysis. The means of each test specimen were submitted to the Kolmogorov-Smirnov test (p > 0.05, ANOVA and Tukey test (p < 0.05. With regard to hardness (F = 86.74, p < 0.0001 the analysis showed significant differences among the resin composite brands. But aging did not influence the hardness of any of the resin composites (F = 0.39, p = 0.53. In this study, there was interaction between the resin composite brand and the aging factors (F = 4.51, p < 0.0002. It was concluded that notwithstanding the type of resin, AAA did not influence surface hardness. However, with regard to hardness there was a significant difference among the resin brands.

  2. Removal of radiocesium using cation exchange resin

    International Nuclear Information System (INIS)

    Morita-Murase, Yuko; Mizumura, Ryosuke; Tachibana, Yoshitaka; Kanazawa, Hideko

    2013-01-01

    Cation exchange resins (calcium polystyrene sulfonate, Ca-resin and sodium polystyrene sulfonate, Na-resin) have been used as agents to improve hyperkerlemia. For removing 137 Cs from the human body, the adsorption ability of the resin for 137 Cs was examined and evaluated. Resin (0.03 g) and 137 Cs (ca.1 kBq) were introduced into 3 mL of water, the Japanese Pharmacopoeia 1st fluid for a dissolution test (pH 1.2) and 2nd fluid (pH 6.8), respectively, and shaken. After 1-3 hours, the 137 Cs adsorption (%) of Na-resin was 99% in water, 60% in a pH 1.2 fluid and, 66% in a pH 6.8 fluid. By adding potassium, the 137 Cs adsorption (%) of Ca-resin was reduced. However, the 137 Cs adsorption (%) of Na-resin was almost unchanged. These results show that both resins have adsorption ability for 137 Cs in the stomach and the intestines. Therefore, the proposed method will be an effective means in the case of a radiological emergency due to 137 Cs. (author)

  3. Magnetic properties and configuration of Fe{sub 50}Pt{sub 50*x}Rh{sub x} films

    Energy Technology Data Exchange (ETDEWEB)

    Fenske, Jochen; Lott, Dieter; Schreyer, Andreas [Helmholt-Zentrum, Geesthacht (Germany); Schmidt, Wolfgang; Schmalzl, Karin [IFF Forschungszentrum, Juelich (Germany); JCNS at ILL (France); Mankey, Gary J. [MINT Center, University of Alabama (United States); Klose, Frank [Ansto, Bragg Institute (Australia); Tartakowskaya, Helena [Institute for Magnetism, National Accademy of Scinece (Ukraine)

    2011-07-01

    Ordered FePt alloys with L1{sub 0} structure are known as materials with FM order and a high magnetic moment of Fe providing a large magnetization. The large atomic number of Pt on the other hand results in a high magnetic anisotropy. If grown in thin films, the high anisotropy often results in perpendicular magnetization which is the preferred orientation for current magnetic recording media. One way to control the magnetic properties in these materials is through the introduction of a third element into the crystal matrix e.g. Rh. When Rh is added to replace Pt in the equiatomic alloy, new magnetic phases emerge. Here we present neutron diffraction studies on the magnetic properties of different 200nm thick Fe{sub 50}Pt{sub 50*x}Rh{sub x} films in dependence of the temperature and external magnetic fields. Additional resonant x-ray measurements on the Fe and Pt absorption edges provide additional information about the magnetic moments on these sites.

  4. Spectrophotometric determination of phosphorus in iron alloys employing a flow injection system

    OpenAIRE

    Gervasio,Ana P. G.; Miranda,Carlos E. S.; Luca,Gilmara C.; Tumang,Cristiane A.; Campos,Luis F. P.; Reis,Boaventura F.

    2001-01-01

    A flow-injection procedure for spectrophotometric determination of phosphorus in electrolytic iron and iron alloys is proposed. The method is based on the ammonium molybdate reaction followed by stannous chloride reduction in acidic medium. In order to circumvent the severe interference caused by the major constituents such as Fe(III) and Cr(III), a mini-column packed with AG50W-X8 resin was coupled to the manifold. A sample throughput of 40 determinations per hour, a dynamical range from P 0...

  5. Crystallization and preliminary X-ray crystallographic analysis of Thermotoga maritima CheA P3-P4-P5 domains in complex with CheW

    International Nuclear Information System (INIS)

    Park, SangYoun; Kim, Keon Young; Kim, Sunmin; Crane, Brian R.

    2012-01-01

    T. maritima CheA P3-P4-P5 domains were crystallized in complex with CheW. Low-resolution diffraction data were collected to ∼8 Å using synchrotron X-ray radiation. The CheA–CheW complex plays a key role in bacterial chemotaxis signal transduction by initiating phosphotransfer to response regulators via coupling to the chemoreceptors. CheA (P3-P4-P5 domains) and CheW from Thermotoga maritima were overexpressed in Escherichia coli and crystallized as a complex at 298 K using ammonium dihydrogen phosphate as a precipitant. X-ray diffraction data were collected to ∼8 Å resolution at 100 K using synchrotron radiation. The crystal belonged to space group I222 or I2 1 2 1 2 1 , with unit-cell parameters a = 184.2, b = 286.4, c = 327.7 Å. The asymmetric unit may contain six to ten CheA–CheW molecules

  6. Determination of tellurium at ultra-trace levels in drinking water by on-line solid phase extraction coupled to graphite furnace atomic absorption spectrometer

    International Nuclear Information System (INIS)

    Pedro, Juana; Stripekis, Jorge; Bonivardi, Adrian; Tudino, Mabel

    2008-01-01

    In this paper, two time-based flow injection (FI) separation pre-concentration systems coupled to graphite furnace atomic absorption spectrometry (GFAAS) for tellurium determination are studied and compared. The first alternative involves the pre-concentration of the analyte onto Dowex 1X8 employed as packaging material of a micro-column inserted in the flow system. The second set-up is based on the co-precipitation of tellurium with La(OH) 3 followed by retention onto XAD resins. Both systems are compared in terms of limit of detection, linear range, RSD%, sample throughput, micro-columns lifetime and aptitude for fully automatic operation. The features of the Dowex system are: 37% efficiency of retention and an enhancement factor of 42 for a pre-concentration time of 180 seconds (sample flow rate = 3 ml min -1 ) with acetic acid elution volumes of 80 μl. The detection limit (3 s) is 7 ng l -1 and the relative standard deviation (n = 7200 ng l -1 ) is 5.8%. The analytical performance of the XAD system is: 72% efficiency of retention and an enhancement factor of 25 for a pre-concentration time of 180 s (sample flow rate = 3 ml min -1 ) with nitric acid elution volumes of 300 μl. The detection limit is 66 ng l -1 and the relative standard deviation (n = 7200 ng l -1 ) is 8.3%. Applications to the determination of tellurium in tap water and the validation of the analytical methodology employing SRM 1643e as certified reference material are shown

  7. Arsenic Removal from Pinctada martensii Enzymatic Hydrolysate by Using Zr(Ⅳ)-Loaded Chelating Resin

    Institute of Scientific and Technical Information of China (English)

    YANG Xiaoman; DAI Wenjin; SUN Huili; PAN Jianyu

    2013-01-01

    The present study investigated the removal of inorganic arsenic from Pinctada martensii enzymatic hydrolysate through unmodified resin (D296) and Zr(Ⅳ)-loaded chelating resin (Zr-D401).By loading Zr to macroporous chelating resin D401,the as exchange adsorption active sites are generated.This transforms D401 from a material that does not have the arsenic adsorption capacity into a material that has excellent arsenic exchange adsorption capacity.The static adsorption experiments were conducted to investigate the optimal removal condition for D296 and Zr-D401.The experimental results show that:the optimum condition for D296 is that T=25℃,pH=5,resin additive amount=1 g(50mL)-1,and contact time=10h,the corresponding arsenic removal rate being 65.7%,and protein loss being 2.33%; the optimum condition for Zr-D401 is that T=25 ℃,pH=8,resin additive amount=1 g (50 mL)-1,and contact time=10 h,the corresponding arsenic removal rate being 70.3%,and protein loss being 4.65%.These results show that both of the two resins are effective in arsenic removal for preserving useful substance.Our research provides scientific evidence and advances in the processing technology for heavy metal removal in shellfish.

  8. The Integration of SME'S into Fusion Projects - Especially for the Manufacturing of Components for W7-X

    International Nuclear Information System (INIS)

    Heyn, K.; Scheller, H.; Andersson, H.

    2006-01-01

    The Consortium of Babcock Noell in Wuerzburg (Germany) and Ansaldo Superconduttori in Genoa (Italy) is producing the 50 nonplanar superconducting coils for the W7-X project. For the realization of the W7-X coils, especially for the manufacturing of the different components, an international network of companies is used, among them several SME's: highly specialized small and medium size enterprises. One of these SME's, which surpassed itself, is the Swedish foundry oesterby Gjuteri AB which has produced the stainless steel coil casings for W7-X. The design of the SS casings was changed by the customer after placing the contact. This has caused the question to manufacture the halfrings with cast segments or as entire castings, which lead finally to the contact with oesterby. A lot of effort was necessary to design the 10 different patterns for the 5 types of casings each consisting of 2 halfrings. The qualification of the SS grade for the high requirements of the project, among them the low cobalt content or the required mechanical properties at 4 K needed some time. Further on a lot of investigations about the test procedures were necessary to be applied for the special geometry of the product, for the 3D measurements or the NDT. The conventional x-ray was not completely suitable for this product due to the thickness of the material in some areas. The main production steps for each halfring will be presented in the paper. The testing includes different NDT, the material tests at RT and 4 K and the 3D measurement. The first casing was delivered end of 2001 and the last in autumn 2005 after several unexpected interruptions. All were treated in a close contact with the customer and in good collaboration between oesterby and BNG and have lead to a significant increase of competence on both sides. Several other SME's are involved in the network for W7-X realization. There are for example: C-CON in Rottenburg and its subcontractors PEM and KUKA in Schwarzenberg for Final

  9. A randomized controlled three year evaluation of "bulk-filled" posterior resin restorations based on stress decreasing resin technology

    DEFF Research Database (Denmark)

    van Dijken, Jan W V; Pallesen, Ulla

    2014-01-01

    -hybrid resin composite (Ceram X mono) layer. In the second cavity, the hybrid resin composite was placed in 2mm increments. The restorations were evaluated using slightly modified USPHS criteria at baseline and then yearly during 3 years. Caries risk and parafunctional habits of the participants were estimated...

  10. Lactobacillus paracasei subsp paracasei L. casei W8 suppresses energy intake acutely

    DEFF Research Database (Denmark)

    Bjerg, Anne Toksvig; Kristensen, Mette Bredal; Ritz, Christian

    2014-01-01

    Background: Probiotic bacteria have been shown to have various effects on the microbiota; this may also affect appetite and may help promote weight loss and maintenance. Objective: This study was conducted to investigate the effect of Lactobacillus paracasei subsp paracasei L. casei W8 (L. casei W8...

  11. A critical analysis of the degree of conversion of resin-based luting cements

    Directory of Open Access Journals (Sweden)

    Jaime Dutra Noronha Filho

    2010-10-01

    Full Text Available OBJECTIVE: This study analyzed the degree of conversion (DC% of four resin-based cements (All Ceram, Enforce, Rely X ARC and Variolink II activated by two modes (chemical and dual, and evaluated the decrease of DC% in the dual mode promoted by the interposition of a 2.0-mm-thick IPS Empress 2 disc. MATERIAL AND METHODS: In the chemical activation, the resin-based cements were prepared by mixing equal amounts of base and catalyst pastes. In the dual activation, after mixing, the cements were light-activated at 650 mW/cm² for 40 s. In a third group, the cements were light-activated through a 2.0-mm-thick IPS Empress 2 disc. The DC% was evaluated in a FT-IR spectrometer equipped with an attenuated total reflectance crystal (ATR. The data were analyzed by two-way ANOVA and Tukey's HSD test. RESULTS: For all resin-based cements, the DC% was significantly higher with dual activation, followed by dual activation through IPS Empress 2, and chemical activation (p<0.05. Irrespective of the activation mode, Rely X presented the highest DC% (p<0.05. Chemically activated Variolink and All Ceram showed the worst results (p<0.05. The DC% decreased significantly when activation was performed through a 2.0-mm-thick IPS Empress 2 disc (p<0.05. CONCLUSION: The results of the present study suggest that resin-based cements could present low DC% when the materials are dually activated through 2.0 mm of reinforced ceramic materials with translucency equal to or less than that of IPS-Empress 2.

  12. Influence of bleaching agents on the microhardness of nanoparticle resin composite

    Directory of Open Access Journals (Sweden)

    Vanderlei Salvador Bagnato

    2009-01-01

    Full Text Available Objective: To assess the effect of bleaching agents on the microhardness of nanoparticle resin composite. Methods: Twenty-eight cylindrical test specimens (8x1mm of FiltekTM Supreme XT resin (3M/ESPE were prepared and divided into 5 groups. The initial Vickers microhardness was measured (load of 50 grams force for 30 seconds on the top surface of the test specimens. The groupswere treated and divided as follows: G1 – artificial saliva (21 days - control; G2 - 7% hydrogen peroxide gel applied for 4h/day, for 14 days; G3 - 10% carbamide peroxide for 4h/day, for 14 days: G4 – 35% hydrogen peroxide gel applied in three sessions of 30 minutes each, with an interval of one week (21 days between the sessions; G5 - 35% carbamide peroxide, three sessions of 30 minutes each, with an interval of one week (21 days between the sessions. The top surfaces of the test specimens received treatment and were submitted to the Vickers microhardness test. Results: The results obtained were submitted to the Analysis of Variance at a fixed criterion, at a level of significance of p=0.05. No significant differences were observed among the treatments tested (p=0.42 when compared with G1. Significant differences (Tukey test were found when the initial microhardness values were compared with the values after experimental treatments (p<0.01. Conclusion: The application of bleaching agents did not alter the microhardness of resin composites. Therefore, there is no need to change restorations after bleaching.

  13. The influence of ceramic surface treatments on the micro-shear bond strength of composite resin to IPS Empress 2.

    Science.gov (United States)

    Panah, Faride Gerami; Rezai, Sosan Mir Mohammad; Ahmadian, Leila

    2008-07-01

    An increasing demand for esthetic restorations has resulted in the development of new ceramic systems, but fracture of veneering ceramics still remains the primary cause of failure. Porcelain repair frequently involves replacement with composite resin, but the bond strength between composite resin and all-ceramic coping materials has not been studied extensively. The purpose of this study was to evaluate the influence of different ceramic surface treatments on the micro-shear bond strength of composite resin to IPS Empress 2 coping material. Sixteen 7 x 7 x 1 mm(3) lithia disilicate-based core ceramic plates were fabricated using the lost wax technique. The plates were divided into eight groups, and eight different surface treatments were performed: (1) no treatment (NT); (2) airborne-particle abrasion with 50-mum alumina particles (Al); (3) acid etching with 9.6% hydrofluoric acid for 1 min (HF); (4) silane coating (S); (5) AlHF; (6) AlS; (7) HFS; and (8) AlHFS. Then, ten composite resin cylinders (0.8-mm diameter x 0.5-mm height) were light-polymerized onto the ceramic plates in each group. Each specimen was subjected to a shear load at a crosshead speed of 0.5 mm/min until fracture occurred. The fracture sites were examined with scanning electron microscopy (SEM) to determine the location of failure during debonding and to examine the surface treatment effects. One-way analysis of variance (ANOVA) and multiple comparison (Dunnet T3) tests were used for statistical analysis of data. The mean micro-shear bond strength values (SD) in MPa were--NT: 4.10 (3.06), Al: 7.56 (4.11), HF: 14.04 (2.60), S: 14.58 (2.14), AlHF: 15.56 (3.36), AlS: 23.02 (4.17), HFS: 24.7 (4.43), AlHFS: 26.0 (3.71). ANOVA indicated the influence of surface treatment was significant (p Empress 2 was significantly different depending on the surface treatment method. Among the investigated methods, silane coating after airborne-particle abrasion and etching was the most effective surface treatment

  14. Applying a method of chemical separation and mass spectrometry for the determination of radium-226 in surface water

    International Nuclear Information System (INIS)

    Sibello Hernandez, Rita Y; Cozzella, Maria Letizia; Guillen Arruebarrena, Aniel

    2014-01-01

    Radium-226 ( 226 Ra) is a naturally occurring radionuclide, alpha emitter with half-life of 1 622 years originating from uranium-238 ( 238 U). Its presence in drinking water is a major radiological hazards, which requires constant monitoring. The analytical techniques used in the determination of 226 Ra generally require the establishment of secular equilibrium and/or tedious separation of other elements. The main objective of this paper is to demonstrate the efficiency and speed of a method of preconcentration and separation of 226 Ra in natural water samples using coprecipitation with MnO 2 radius and purification by cation exchange resin Dowex 50WX8. Measurement technique was Quadrupole Mass Spectrometry and associated induced plasma ICP-Q-MS. The 226 Ra values obtained are in the range of 0,010-0,219 pg/L in natural waters analyzed

  15. Effect of resin cement, aging process and root level on the bond strength of the resin-fiber posts

    Science.gov (United States)

    Almuhim, Khalid Salman

    Background. Little is known about the long-term clinical bonding effectiveness of the Fiber-reinforced composite (FRC) posts cemented with self-etch adhesive systems. Bond stability and longevity of the cemented post are adversely affected by physical and chemical factors over time, such as expansion and contraction stresses caused by thermal changes and occlusal load. This clinical condition can be simulated in vitro by thermocyclic loading; and bonding effectiveness can be evaluated by applying the micropush out test. Therefore, more in vitro studies are needed to evaluate the bond strength of the fiber posts cemented with different resin cement systems after simulating the artificial aging induced by thermocycling. The aim of this study was to compare the microtensile bond strength of two different resin cement systems (total etch, and self-etch resin cement system) used for cementation of fiber reinforced composite posts in three different aging periods using thermocycling. Methods. Following IRB approval, sixty freshly extracted bicuspid single rooted natural teeth were endodontically treated, and the post-spaces were prepared to receive a fiber-post cemented with either a total etch resin cement (Rely-X Ultimate) or with a self-etch resin cement (Rely-X Unicem). No thermocycling, 20,000 and 40,000 cycles was used to age the specimens. Teeth were randomly allocated into six different groups: G1 - Control: Rely-X Ultimate cement with no thermocycling. G2: Rely-X Ultimate cement with 20,000 thermocycling. G3: Rely-X Ultimate cement with 40,000 thermocycling. G4: Rely-X Unicem cement. G5: Rely-X Unicem cement. G6: Rely-X Unicem cement. Microtensile bond strength determined using a micropush out test on a universal testing machine (MTS). Additionally, the failure mode of each specimen was observed under a stereomicroscope (Olympus) at 40x magnification. Finally, one representative sample was randomly selected from each of the five failure modes for scanning

  16. Biodiesel production from acid oils and ethanol using a solid basic resin as catalyst

    International Nuclear Information System (INIS)

    Marchetti, J.M.; Errazu, A.F.

    2010-01-01

    In the search of an alternative fuel to substitute diesel fuel, biodiesel appears as one of the most promising sources of energy for diesel engines because of its environmental advantages and also due to the evolution of the petroleum market. Refined oil is the conventional raw material for the production of this biofuel; however, its major disadvantage is the high cost of its production. Therefore, frying oils, waste oils, crude oils and/or acid oils are being tested as alternative raw materials; nevertheless, there will be some problems if a homogeneous basic catalyst (NaOH) is employed due to the high amount of free fatty acid present in the raw oil. In this work, the transesterification reaction of acid oil using solid resin, Dowex monosphere 550 A, was studied as an alternative process. Ethanol was employed to have a natural and sustainable final product. The reaction temperature's effects, the initial amount of free fatty acid, the molar ratio of alcohol/oil and the type of catalyst (homogeneous or heterogeneous) over the main reaction are analyzed and their effects compared. The results obtained show that the solid resin is an alternative catalyst to be used to produce fatty acid ethyl esters (FAEEs) by a transesterification reaction with a final conversion over 90%. On the other hand, the time required to achieve this conversion is bigger than the one required using conventional technology which employs a homogeneous basic catalyst. This reaction time needs to be optimized. (author)

  17. Effect of autoclave postpolymerization treatments on the fracture toughness of autopolymerizing dental acrylic resins.

    Science.gov (United States)

    Durkan, Rukiye; Gürbüz, Ayhan; Yilmaz, Burak; Özel, M Birol; Bağış, Bora

    2012-06-26

    Microwave and water bath postpolymerization have been suggested as methods to improve the mechanical properties of heat and autopolymerizing acrylic resins. However, the effects of autoclave heating on the fracture properties of autopolymerizing acrylic resins have not been investigated. The aim of this study was to assess the effectiveness of various autoclave postpolymerization methods on the fracture properties of 3 different autopolymerizing acrylic resins. Forty-two specimens of 3 different autopolymerizing acrylic resins (Orthocryl, Paladent RR and Futurajet) were fabricated (40x8x4mm), and each group was further divided into 6 subgroups (n=7). Control group specimens remained as processed (Group 1). The first test group was postpolymerized in a cassette autoclave at 135°C for 6 minutes and the other groups were postpolymerized in a conventional autoclave at 130°C using different time settings (5, 10, 20 or 30 minutes). Fracture toughness was then measured with a three-point bending test. Data were analyzed by ANOVA followed by the Duncan test (α=0.05). The fracture toughness of Orthocryl and Paladent-RR acrylic resins significantly increased following conventional autoclave postpolymerization at 130°C for 10 minutes (Pautoclave postpolymerized Futurajet was not significantly different than its control specimens (Pautoclaved at 130°C for 10 minutes. Within the limitations of this study, it can be suggested that autoclave postpolymerization is an effective method for increasing the fracture toughness of tested autoploymerized acrylic resins.

  18. Beam Transport Devices for the 10 kW IR Free Electron Laser

    International Nuclear Information System (INIS)

    Lawrence Dillon-Townes; Michael Bevins; David Kashy; Stephanie Slachtouski; Ronald Lassiter; George Neil; Michelle Shinn; Joseph Gubeli; Christopher Behre; David Douglas; David W. Waldman; George Biallas; Lawrence Munk; Christopher Gould

    2005-01-01

    Beam transport components for the 10kW IR Free Electron Laser (FEL) at Thomas Jefferson National Accelerator Facility (Jefferson Lab) were designed to manage (1) electron beam transport and (2) photon beam transport. An overview of the components will be presented in this paper. The electron beam transport components were designed to address RF heating, maintain an accelerator transport vacuum of 1 x 10 -8 torr, deliver photons to the optical cavity, and provide 50 kW of beam absorption during the energy recovery process. The components presented include a novel shielded bellows, a novel zero length beam clipper, a one decade differential pumping station with a 7.62 cm (3.0 inch) aperture, and a 50 kW beam dump. The photon beam transport components were designed to address the management of photons delivered by the accelerator transport. The optical cavity manages the photons and optical transport delivers the 10 kW of laser power to experimental labs. The optical cavity component presented is a unique high reflector vessel and the optical transport component presented is a turning mirror cassette

  19. Rattling of Ba-atoms in Ba8ZnxGe43-5x/8([]3-3x/8)

    International Nuclear Information System (INIS)

    Melnychenko, N.; Grytsiv, A.; Rotter, M.; Rogl, P.; Devishvili, A.

    2006-01-01

    Full text: In order to improve the figure of merit of thermoelectric materials, one of the key parameters to be minimized is the lattice thermal conductivity. It is thus essential for the design of new thermoelectric materials to understand the lattice dynamics, especially the scattering mechanism of low energy phonons. The present paper describes formation, phase relations at subsolidus temperatures as well as at 800 o C, crystal chemistry and physical properties of a series of ternary clathrates as part of the solid solution, Ba 8 Zn x (Ge 43-5x/8[]3-3x/8 ), deriving from binary Ba 8 Ge 43 []3 with a solubility limit of 8 Zn per formula unit at 800 o C. Structural investigations in all cases confirm cubic primitive symmetry with a lattice parameter a ∼ 1.1 nm consistent with the space group type Pm-3n. Studies of transport coefficients evidence electrons as the majority charge carriers in the systems. Thermal conductivity exhibits a pronounced low temperature maximum, dominated by the lattice contribution, while at higher temperatures the electronic part gains weight. Inelastic neutron scattering experiments are used to study the phonon spectrum for Ba 8 Zn 8 Ge 38 . (author)

  20. Hydrogen permeation in asymmetric La28-xW4 + xO54 + 3x/2 membranes

    DEFF Research Database (Denmark)

    Gil, Vanesa; Gurauskis, Jonas; Kjølseth, Christian

    2013-01-01

    Asymmetric supported La28 - xW4 + xO 54 + 3x/2 (La/W ≈ 5.6) membranes were investigated for their hydrogen permeation properties as a function of temperature and feed gas conditions. Dense membranes of thickness 25-30 μm supported on substrates with 25 and 40 vol.% porosity were compared. Above 850...

  1. Thermal properties of Avery Island salt to 5730K and 50-MPa confining pressure

    International Nuclear Information System (INIS)

    Durham, W.B.; Abey, A.E.

    1981-01-01

    Thermal conductivity, thermal diffusivity, and thermal linear expansion were measured on two samples of Avery Island rock salt up to simultaneous temperatures and pressures of 573 0 K and 50 MPa. Thermal conductivity at room temperature measured 6.3 +- 0.6 W/mK and decreased monotonically to 3.3 +- 0.4 W/mK at 573 0 K. Thermal diffusivity decreased from 3.0 +- 0.8 x 10 -6 m 2 /s at room temperature to 1.4 +- 0.5 x 10 -6 m 2 /s at 573 0 K. Thermal linear expansivity increased from 4.8 +- 0.3 x 10 -5 K -1 at room temperature to 5.6 +- 0.3 x 10 -5 K -1 at 573 0 K. The thermal properties showed no measurable (+-5%) dependence on confining pressure from 0 to 50 MPa for any temperature tested. The thermal conductivity values were not distinguishable (+-5%) from intrinsic (single crystal) values measured by others. Diffusivity fell about 20% below intrinsic values, and linear expansivity about 20% above intrinsic values. Thermal conductivity values for Avery Island salt measured recently by Morgan are as much as 50% lower than values measured here and were probably strongly affected by sample handling prior to measurement. The pressure independence of the thermal properties measured in our study suggests that thermally-induced microfracturing is nearly nonexistent. This lack of thermal cracking is consistent with the high (cubic) symmetry of halite

  2. Effect of surface treatment of FRC-Post on bonding strength to resin cements

    Directory of Open Access Journals (Sweden)

    Chan-Hyun Park,

    2011-03-01

    Full Text Available Objectives The purpose of this study was to evaluate the effect of surface treatment of FRC-Post on bonding strength to resin cements. Materials and Methods Pre-surface treated LuxaPost (DMG, Rely-X Fiber Post (3M ESPE and self adhesive resin cement Rely-X Unicem (3M ESPE, conventional resin cement Rely-X ARC (3M ESPE, and Rely-X Ceramic Primer (3M ESPE were used. After completing the surface treatments of the posts, posts and resin cement were placed in clear molds and photo-activation was performed. The specimens were sectioned perpendicular to the FRC-Post into 2 mm-thick segments, and push-out strength were measured. The results of bond strength value were statistically analyzed using independent samples t-test and one-way ANOVA with multiple comparisons using Scheffe's test. Results Silanization of posts affect to the bond strength in LuxaPost, and did not affect in Rely-X Fiber Post. Rely-X ARC showed higher value than Rely-X Unicem. Conclusions Silanization is needed to enhance the bond strength between LuxaPost and resin cements.

  3. Scintillation hodoscope with working area of 50 x 50 cm based on hodoscopic photomultipliers

    International Nuclear Information System (INIS)

    Borog, V.V.; Vasil'chenko, V.G.; Demekhin, A.V.; Dronov, V.V.; Rykalin, V.I.

    1987-01-01

    The choice of optimum designs for the sensitive elements of large hodoscopes based on hodoscopic photomultipliers is examined. The results of numerical calculations are confirmed by measurement results. The measured space resolution of one of the scintillation-hodoscope designs (with two hodoscopic photomultipliers) with a sensitive volume of 50 x 50 x 2 mm is ≤ +3 mm

  4. Results from X-ray measurements on the Wendelstein W7-AS stellarator

    International Nuclear Information System (INIS)

    Weller, A.; Brakel, R.; Burhenn, R.; Hacker, H.; Lazaros, A.

    1991-01-01

    X-ray imaging measurements have contributed to studies of the plasma equilibrium, plasma fluctuations, impurity radiation and impurity transport effects in the advanced stellarator Wendelstein W7-AS (R = 2 m, a = 17 cm). In addition, time resolved electron temperature profiles are deduced from X-ray intensity ratios according to the two absorber foil method. The plasma is generated and heated by fundamental and 2nd harmonic ECRH (P ≤ 800 kW at 70 GHz). Neutral beam injection heating (P ≤ 1.5 MW) was applied also, assisted by D 2 pellet injection. (orig.)

  5. Effects of Core-Shell Rubber (CSR) Nanoparticles on the Fracture Toughness of an Epoxy Resin at Cryogenic Temperatures

    Science.gov (United States)

    Wang, J.; Cannon, S. A.; Schneider, J. A.

    2008-01-01

    This study investigates the effects of core-shell rubber (CSR) nanoparticles on the fracture toughness of an epoxy resin at liquid nitrogen (LN2) temperatures. Varying amounts of Kane Ace (Registered TradeMark) MX130 toughening agent were added to a commercially available EPON 862/W epoxy resin. Resulting fracture toughness was evaluated by the use of Charpy impact tests conducted on an instrumented drop tower. The size and distribution of the CSR nanoparticles were characterized using Transmission Electric Microscopy (TEM) and Small Angle X-ray Scattering (SAXS). Up to nominal 4.6% addition of the CSR nanoparticles, resulted in a nearly 5 times increase in the measured breaking energy. However, further increases in the amount of CSR nanoparticles had no appreciable affect on the breaking energy.

  6. A valuable new essential oil from the resin of Altingia siamensis Craib. from Vietnam

    NARCIS (Netherlands)

    Chinh, N.D.; Dung, N.X.; Leclercq, P.A.

    1994-01-01

    More than 30 components were identified in the essential oil of A. siamensis resin from Vietnam by a combination of high resoln. GC and GC/MS. The major compds. were a-copaene (9.6%), a-humulene (8.5%), junenol (6.8%), b-caryophyllene (6.6%), b-bisabolene (5.5%) and (E,E)-a-farnesene (5.0%). The oil

  7. 50 CFR 35.8 - Forest management.

    Science.gov (United States)

    2010-10-01

    ... 50 Wildlife and Fisheries 6 2010-10-01 2010-10-01 false Forest management. 35.8 Section 35.8... NATIONAL WILDLIFE REFUGE SYSTEM WILDERNESS PRESERVATION AND MANAGEMENT General Rules § 35.8 Forest management. Forest management activities in a wilderness unit will be directed toward allowing natural...

  8. Ion Exchange Temperature Testing with SRF Resin - 12088

    Energy Technology Data Exchange (ETDEWEB)

    Russell, R.L.; Rinehart, D.E.; Brown, G.N.; Peterson, R.A. [Pacific Northwest National Laboratory, Richland, WA 99352 (United States)

    2012-07-01

    Ion exchange using the Spherical Resorcinol-Formaldehyde (SRF) resin has been selected by the U.S. Department of Energy's Office of River Protection for use in the Pretreatment Facility of the Hanford Tank Waste Treatment and Immobilization Plant (WTP) and for potential application in an at-tank deployment for removing Cs-137. Recent proposed changes to the WTP ion exchange process baseline indicate that higher temperatures (50 deg. C) to alleviate post-filtration precipitation issues prior to reaching the ion exchange columns may be required. Therefore, it is important to understand the behavior of SRF resin performance under the conditions expected with the new equipment and process changes. This research examined the impact of elevated temperature on resin loading and resin degradation during extended solution flow at elevated temperature (45 deg., 50 deg., 55 deg., 60 deg., 65 deg., 75 deg. C). Testing for extended times at elevated temperatures showed that the resin does degrade and loading capacity is reduced at and above 45 deg. C. Above 60 deg. C the resin appears to not load at all. It was observed that the resin disintegrated at 75 deg. C until not much was left and partially disintegrated at 65 deg. C, which caused the column to plug in both tests after ∼336 hours. The results indicate that WTP will lose resin loading capacity if the ion exchange process is performed above 25 deg. C, and the resin will disintegrate above 65 deg. C. Therefore, WTP will have a restricted operating range of temperatures to perform the ion exchange process with this resin. PNNL and WTP are currently evaluating the operating limits of the resin in further detail. Aging in 0.5 M HNO{sub 3} also caused the resin to lose capacity above 25 deg. C and to completely dissolve at 55 deg. C. Again, WTP will have a restricted operating range of temperatures when eluting the resin with nitric acid in order to maintain resin loading capacity and avoid disintegration of the resin

  9. Orifice Mass Flow Calculation in NASA's W-8 Single Stage Axial Compressor Facility

    Science.gov (United States)

    Bozak, Richard F.

    2018-01-01

    Updates to the orifice mass flow calculation for the W-8 Single Stage Axial Compressor Facility at NASA Glenn Research Center are provided to include the effect of humidity and incorporate ISO 5167. A methodology for including the effect of humidity into the inlet orifice mass flow calculation is provided. Orifice mass flow calculations provided by ASME PTC-19.5-2004, ASME MFC-3M-2004, ASME Fluid Meters, and ISO 5167 are compared for W-8's atmospheric inlet orifice plate. Differences in expansion factor and discharge coefficient given by these standards give a variation of about +/- 75% mass flow except for a few cases. A comparison of the calculations with an inlet static pressure mass flow correlation and a fan exit mass flow integration using test data from a 2017 turbofan rotor test in W-8 show good agreement between the inlet static pressure mass flow correlation, ISO 5167, and ASME Fluid Meters. While W-8's atmospheric inlet orifice plate violates the pipe diameter limit defined by each of the standards, the ISO 5167 is chosen to be the primary orifice mass flow calculation to use in the W-8 facility.

  10. Application of 15N amino acid absorption in chronic enteropathy and hepatic diseases in infants

    International Nuclear Information System (INIS)

    Culea, M.; Palibroda, N.; Chiriac, M.; Moldovan, Z.; Miu, N.

    1993-01-01

    The aim of this study was to estimate malabsorption status in humans using a 15 N stable isotope tracer technique. [ 15 N]-glycine, 98.98 atom %, was synthesized in our institute and was administered orally as a single bolus dose to twelve patients. Six of the 12 subjects studied were healthy and 6 were suspected of having malabsorption. Blood, urine and faecal samples were obtained, proteins in the samples were precipitated with sulphosalicylic acid (5%), the eluate was purified with Dowex 50W-X8 (40mm x 2mm column), and derivatised to form the trifluoroacetyl-butyl esters using standard techniques. Gas chromatographic separation was performed on a glass column 2m X 3mm i.d. packed with EGA 1% on Chromosorb W AW 80-100 mesh. An isotope dilution GC/MS method and Kjeldahl digestion followed by MS analysis of nitrogen gas was performed. 15 N isotopomer was used as internal standard. [ 15 N]-Gly elimination in faeces was compared with total 15 N elimination in faeces to distinguish artefacts caused by intestinal bacteria. Significant differences in the amount of [ 15 N]-Gly eliminated in urine and faeces between malabsorption and control patients were obtained. It was concluded that more emphasis should be given to the faeces data than to urine because 15 N elimination in urine is competitive with 15 N incorporation into protein. 12 refs, 4 figs, 4 tabs

  11. Rapid and sensitive determination of beta-phenylethylamine in animal brains by high performance liquid chromatography with fluorometric detection.

    Science.gov (United States)

    Taga, C; Tsuji, M; Nakajima, T

    1989-05-01

    A reversed phase HPLC method with fluorometric detection for the analysis of beta-phenylethylamine has been developed using p-methoxyphenylethylamine as an internal standard. Two columns, containing 200 microL of Dowex 50-X8 and Amberlite CG-50 respectively, were used to prepare a fraction containing beta-phenylethylamine. The recoveries of beta-phenylethylamine and p-methoxyphenylethylamine were 53.9 +/- 9.4% and 68.1 +/- 12.4%, respectively, and elution profile of p-methoxyphenylethylamine was sufficiently well correlated with that of beta-phenylethylamine. Regional distributions of beta-phenylethylamine in rat and mouse brains were determined. The highest concentrations were found in hypothalamus and hippocampus in both animals.

  12. A 50-kW Module Power Station of Directly Solar-Pumped Iodine Laser

    Science.gov (United States)

    Choi, S. H.; Lee, J. H.; Meador, W. E.; Conway, E. J.

    1997-01-01

    The conceptual design of a 50 kW Directly Solar-Pumped Iodine Laser (DSPIL) module was developed for a space-based power station which transmits its coherent-beam power to users such as the moon, Martian rovers, or other satellites with large (greater than 25 kW) electric power requirements. Integration of multiple modules would provide an amount of power that exceeds the power of a single module by combining and directing the coherent beams to the user's receiver. The model developed for the DSPIL system conservatively predicts the laser output power (50 kW) that appears much less than the laser output (93 kW) obtained from the gain volume ratio extrapolation of experimental data. The difference in laser outputs may be attributed to reflector configurations adopted in both design and experiment. Even though the photon absorption by multiple reflections in experimental cavity setup was more efficient, the maximum secondary absorption amounts to be only 24.7 percent of the primary. However, the gain volume ratio shows 86 percent more power output than theoretical estimation that is roughly 60 percent more than the contribution by the secondary absorption. Such a difference indicates that the theoretical model adopted in the study underestimates the overall performance of the DSPIL. This fact may tolerate more flexible and radical selection of design parameters than used in this design study. The design achieves an overall specific power of approximately 5 W/kg and total mass of 10 metric tons.

  13. Examining exposure reciprocity in a resin based composite using high irradiance levels and real-time degree of conversion values.

    Science.gov (United States)

    Selig, Daniela; Haenel, Thomas; Hausnerová, Berenika; Moeginger, Bernhard; Labrie, Daniel; Sullivan, Braden; Price, Richard B T

    2015-05-01

    Exposure reciprocity suggests that, as long as the same radiant exposure is delivered, different combinations of irradiance and exposure time will achieve the same degree of resin polymerization. This study examined the validity of exposure reciprocity using real time degree of conversion results from one commercial flowable dental resin. Additionally a new fitting function to describe the polymerization kinetics is proposed. A Plasma Arc Light Curing Unit (LCU) was used to deliver 0.75, 1.2, 1.5, 3.7 or 7.5 W/cm(2) to 2mm thick samples of Tetric EvoFlow (Ivoclar Vivadent). The irradiances and radiant exposures received by the resin were determined using an integrating sphere connected to a fiber-optic spectrometer. The degree of conversion (DC) was recorded at a rate of 8.5 measurements a second at the bottom of the resin using attenuated total reflectance Fourier Transform mid-infrared spectroscopy (FT-MIR). Five specimens were exposed at each irradiance level. The DC reached after 170s and after 5, 10 and 15 J/cm(2) had been delivered was compared using analysis of variance and Fisher's PLSD post hoc multiple comparison tests (alpha=0.05). The same DC values were not reached after the same radiant exposures of 5, 10 and 15 J/cm(2) had been delivered at an irradiance of 3.7 and 7.5 W/cm(2). Thus exposure reciprocity was not supported for Tetric EvoFlow (p<0.05). For Tetric EvoFlow, there was no significant difference in the DC when 5, 10 and 15J/cm(2) were delivered at irradiance levels of 0.75, 1.2 and 1.5 W/cm(2). The optimum combination of irradiance and exposure time for this commercial dental resin may be close to 1.5 W/cm(2) for 12s. Copyright © 2015 Academy of Dental Materials. Published by Elsevier Ltd. All rights reserved.

  14. Doping dependent magnetism and exchange bias in CaMn{sub 1−x}W{sub x}O{sub 3} manganites

    Energy Technology Data Exchange (ETDEWEB)

    Markovich, V., E-mail: markoviv@bgu.ac.il; Gorodetsky, G. [Department of Physics, Ben-Gurion University of the Negev, 84105 Beer-Sheva (Israel); Fita, I. [Institute of Physics, Polish Academy of Sciences, Aleja Lotnikow 32/46, PL-02-668 Warsaw (Poland); Donetsk Institute for Physics and Technology, National Academy of Sciences, 83114 Donetsk (Ukraine); Wisniewski, A.; Puzniak, R. [Institute of Physics, Polish Academy of Sciences, Aleja Lotnikow 32/46, PL-02-668 Warsaw (Poland); Mogilyansky, D. [The Ilse Katz Institute for Nanoscale Science and Technology, Ben-Gurion University of the Negev, Beer-Sheva 84105 (Israel); Naumov, S. V.; Mostovshchikova, E. V.; Telegin, S. V. [Institute of Metal Physics, Ural Branch of RAS, Kovalevskaya Street 18, Ekaterinburg 620990 (Russian Federation); Jung, G. [Department of Physics, Ben-Gurion University of the Negev, 84105 Beer-Sheva (Israel); Institute of Physics, Polish Academy of Sciences, Aleja Lotnikow 32/46, PL-02-668 Warsaw (Poland)

    2014-09-07

    Magnetic properties of CaMn{sub 1−x}W{sub x}O{sub 3} (0 ≤ x ≤ 0.1) have been investigated, and the research was focused on the exchange bias (EB) phenomenon in CaMn{sub 0.93}W{sub 0.07}O{sub 3}. Magnetic ground state was found to be dependent on tungsten doping level and the following states were distinguished: (i) G-type antiferromagnetic (AFM) state with a weak ferromagnetic (FM) component at x = 0 and 0.04; (ii) mostly orbitally ordered C-type AFM at x = 0.07 and 0.1. For the studied manganites, spontaneous magnetization increases sharply with increasing doping level reaching M{sub 0} ≈ 9.5 emu/g at T = 10 K for x = 0.04, and then decreases rapidly reaching zero for x = 0.1. Exchange bias effect, manifested by vertical and horizontal shifts in the hysteresis loop for field cooled sample, has been observed in CaMn{sub 0.93}W{sub 0.07}O{sub 3}. Exchange bias field, coercivity, remanence asymmetry, and magnetic coercivity depend strongly on temperature, cooling field, and maximal measuring field. Horizontal and vertical shifts of magnetization loop sharply decrease with increasing temperature and vanish above 70 K, whereas coercivity and magnetic coercivity disappear only above 100 K (temperature of transition to the G-type AFM state). The exchange bias field H{sub EB} increases with increasing cooling field H{sub cool} and goes through a broad maximum at 40 kOe, while the remanence asymmetry increases monotonously in the entire investigated cooling field range, up to 50 kOe. For the compound with x = 0.07, the size of the FM regions ≈2 nm was estimated from the dependence of exchange bias field H{sub EB} upon H{sub cool}. It is suggested that the exchange bias originates from interface exchange coupling between small FM clusters and the G-type AFM phase inside the primary C-type orbitally ordered AFM phase.

  15. Plutonium scrap processing at the Los Alamos Scientific Laboratory

    International Nuclear Information System (INIS)

    Nixon, A.E.; McKerley, B.J.; Christensen, E.L.

    1980-01-01

    The Los Alamos Scientific Laboratory currently has the newest plutonium handling facility in the nation. Los Alamos has been active in the processing of plutonium almost since the discovery of this man-made element in 1941. One of the functions of the new facility is the processing of plutonium scrap generated at LASL and other sites. The feed for the scrap processing program is extremely varied, and a wide variety of contaminants are often encountered. Depending upon the scrap matrix and contaminants present, the majority of material receives a nitric acid/hydrofluoric acid or nitric acid/calcium fluoride leach. The plutonium nitrate solutions are then loaded onto an anion exchange column charged with DOWEX 1 x 4, 50 to 100 mesh, nitrate form resin. The column is eluted with 0.48 M hydroxyl amine nitrate. The Pu(NO 3 ) 3 is then precipitated as plutonium III oxalate which is calcined at 450 to 500 0 C to yield a purified PuO 2 product

  16. Reinforcement of a PMMA resin for interim fixed prostheses with silica nanoparticles.

    Science.gov (United States)

    Topouzi, Marianthi; Kontonasaki, Eleana; Bikiaris, Dimitrios; Papadopoulou, Lambrini; Paraskevopoulos, Konstantinos M; Koidis, Petros

    2017-05-01

    Fractures in long span provisional/interim restorations are a common complication. Adequate fracture toughness is necessary to resist occlusal forces and crack propagation, so these restorations should be constructed with materials of improved mechanical properties. The aim of this study was to investigate the possible reinforcement of neat silica nanoparticles and trietoxyvinylsilane-modified silica nanoparticles in a PMMA resin for fixed interim restorations. Composite PMMA-Silica nanoparticles powders were mixed with PMMA liquid and compact bar shaped specimens were fabricated according to the British standard BS EN ISO 127337:2005. The single-edge notched method was used to evaluate fracture toughness (three-point bending test), while the dynamic thermomechanical properties (Storage Modulus, Loss Modulus, tanδ) of a series of nanocomposites with different amounts of nanoparticles (0.25%, 0.50%, 0.75%, 1% w.t.) were evaluated. Statistical analysis was performed and the statistically significant level was set to pPMMA resins used in fixed provisional restorations. Copyright © 2017 Elsevier Ltd. All rights reserved.

  17. M = Mo, W; X = S, Se, Te) heterostructures

    KAUST Repository

    Zhang, Qingyun

    2018-04-16

    Using first-principles calculations, we investigate the electronic properties of the two-dimensional GaX/MX2 (M = Mo, W; X = S, Se, Te) heterostructures. Orbital hybridization between GaX and MX2 is found to result in Rashba splitting at the valence-band edge around the Γ point, which grows for increasing strength of the spin-orbit coupling in the p orbitals of the chalcogenide atoms. The location of the valence-band maximum in the Brillouin zone can be tuned by strain and application of an out-of-plane electric field. The coexistence of Rashba splitting (in-plane spin direction) and band splitting at the K and K′ valleys (out-of-plane spin direction) makes GaX/MX2 heterostructures interesting for spintronics and valleytronics. They are promising candidates for two-dimensional spin-field-effect transistors and spin-valley Hall effect devices. Our findings shed light on the spin-valley coupling in van der Waals heterostructures.

  18. 21 CFR 177.1655 - Polysulfone resins.

    Science.gov (United States)

    2010-04-01

    ... disodium salt of 4,4′-isopropylidenediphenol is made to react with 4,4′-dichlorodiphenyl sulfone in such a... Limitations Dimethyl sulfoxide Not to exceed 50 parts per million as residual solvent in finished basic resin... residual solvent in finished basic resin in paragraph (a)(1) of this section. N-methyl-2-pyrrolidone Not to...

  19. Preparation Of Phosphorus-32 (P-32) From Irradiated Target P2O5 For Therapeutic Purposes In Nuclear Medicine

    International Nuclear Information System (INIS)

    Nguyen Dang Khoa; Chu Van Khoa; Duong Van Dong

    2011-01-01

    Phosphorus-32 is produced using the nuclear reaction 31 P (n,γ) 32 P by irradiation of the phosphorus peroxide (P 2O 5) target. Phosphoric acid is prepared by the dissolution of irradiated target in 40 ml of boiling chloric acid 0.1 N. When the dissolution of phosphor peroxide is completed, the beaker is allowed to cool. 8 ml of 30% H 2 O 2 is added and refluxed for 3 h. Finally, the solution is filtered through a sintered glass filter, porosity G3 and passed into a column of cationic exchanger (Dowex-50 W-X4 preconditioned in hydrogen form) to remove metallic impurities. The effluent is collected as the stock solution. Radiochemical purity is determined by paper chromatography (radiochemical purity control) in the solvent system: Whatman No. 1 paper and the mixture of isopropyl alcohol : water : 50% trichloracetic acid : 25% NH 4 OH (75:15:10:0.3 v/v.) as a mobile phase, developing time ranged from 12 to 17 h. Radiochemical purity of phosphoric acid (H 3 32 PO 4 ) solution prepared by our method is obtained more than 99%. (author)

  20. Synthesis, magnetism and electronic structure of YbNi{sub 2-x}Fe{sub x}Al{sub 8} (x=0.91) isolated from Al flux

    Energy Technology Data Exchange (ETDEWEB)

    Xiuni, Wu [Department of Physical Sciences, Rhode Island College, Providence, RI 02908 (United States); Francisco, Melanie [Department of Chemistry, Northwestern University, Evanston, IL 60208 (United States); Rak, Zsolt [Department of Physics, Michigan State University, East Lansing, MI 48824 (United States); Bakas, T [Department of Physics, University of Ioannina, GR-45110 Ioannina (Greece); Mahanti, S D [Department of Physics, Michigan State University, East Lansing, MI 48824 (United States); Kanatzidis, Mercouri G. [Department of Chemistry, Northwestern University, Evanston, IL 60208 (United States)], E-mail: m-kanatzidis@northwestern.edu

    2008-12-15

    The combination of ytterbium, nickel, iron in liquid aluminum resulted in the formation of the new intermetallic compound YbNi{sub 2-x}Fe{sub x}Al{sub 8} (x=0.91) which adopts the CaCo{sub 2}Al{sub 8} structure type with a=14.458(3) A, b=12.455(3) A, c=3.9818(8) A and space group Pbam. Its resistivity drops with decreasing temperature, saturating to a constant value at lower temperatures. Above 50 K, the inverse magnetic susceptibility data follows Curie-Weiss Law, with a calculated {mu}{sub eff}=2.19 {mu}{sub B}. Although the observed reduced moment in magnetic susceptibility measurement suggests that the Yb ions in this compound are of mixed-valent nature, ab initio electronic structure calculations within density functional theory using LDA+U approximation give an f{sup 13} configuration in the ground state. - Graphical abstract: The reaction of ytterbium, nickel, iron in aluminum flux gives crystals of the intermetallic compound YbNi{sub 2-x}Fe{sub x}Al{sub 8} (x=0.96) which adopts the CaCo{sub 2}Al{sub 8} structure, ab initio electronic structure calculations within density functional theory using LDA+U approximation suggest an f{sup 13} configuration in the ground state.

  1. Microhardness of resin composite materials light-cured through fiber reinforced composite.

    NARCIS (Netherlands)

    Fennis, W.M.M.; Ray, N.J.; Creugers, N.H.J.; Kreulen, C.M.

    2009-01-01

    OBJECTIVES: To compare polymerization efficiency of resin composite basing materials when light-cured through resin composite and fiber reinforced composite (FRC) by testing microhardness. METHODS: Simulated indirect restorations were prepared by application of resin composite (Clearfil AP-X) or FRC

  2. Structures of Ta22W4O67 and Ta74W6O203. Pt. 1. Refined structural models using synchrotron radiation

    International Nuclear Information System (INIS)

    Schmid, S.

    1995-01-01

    The crystal structures of Ta 22 W 4 O 67 [M r = 5788.19, a = 6.1485 (5), b = 47.6205 (12), c = 3.8559 (3) A, γ = 90.04 (1) , space group = C112/m (non-standard setting), Z = 1, D x = 8.513 g cm -3 , F(000) = 2438] and Ta 74 W 6 O 203 [M r = 17741.06, a = 6.1664 (5), b = 29.2717 (14), c = 3.8731 (2) A, space group = Pbam (no. 55), Z = 0.2, D x = 8.428 g cm -3 , F(000) 1494] were determined using synchrotron radiation at four different wavelengths below the Ta L III edge [λ = 1.2741 (-146 eV), λ = 1.2586 (-26 eV), λ = 1.2571 (-14 eV) and λ = 1.2563 A (-8 eV)]. The collection of data immediately below the Ta L III edge at -8 eV enabled resolution of Ta and W of up to eight electrons, which assisted in the refinement of Ta/W ordering for both structures. Bond valence arguments have been used to locate oxygen vacancies required by the formulae. From the largest data set for Ta 22 W 4 O 67 (λ = 1.2741 A), a final value of 0.0481 for R 1 = Σ parallel F obs (h)vertical stroke - vertical stroke F calc (h) parallel /Σvertical stroke F obs (h)vertical stroke was obtained for 3082 unmerged reflections with I(h) > 3σ[I(h)] and for Ta 74 W 6 O 203 (λ = 1.2563 A) a final value of 0.0571 for R 1 was obtained for 5675 unmerged reflections. The two structures are described from a conventional polyhedral perspective as 13- and 8-times superstructures occurring in the solid solution (1-x)Ta 2 O 5 xWO 3 , 0 ≤ x ≤ 0.267. (orig.)

  3. Enhanced vanillin production from recombinant E. coli using NTG mutagenesis and adsorbent resin.

    Science.gov (United States)

    Yoon, Sang-Hwal; Lee, Eun-Gyeong; Das, Amitabha; Lee, Sook-Hee; Li, Cui; Ryu, Hee-Kyoung; Choi, Myung-Suk; Seo, Weon-Taek; Kim, Seon-Won

    2007-01-01

    Vanillin production was tested with different concentrations of added ferulic acid in E. coli harboring plasmid pTAHEF containing fcs (feruloyl-CoA synthase) and ech (enoyl-CoA hydratase/aldolase) genes cloned from Amycolatopsis sp. strain HR104. The maximum production of vanillin from E. coli DH5alpha harboring pTAHEF was found to be 1.0 g/L at 2.0 g/L of ferulic acid for 48 h of culture. To improve the vanillin production by reducing its toxicity, two approaches were followed: (1) generation of vanillin-resistant mutant of NTG-VR1 through NTG mutagenesis and (2) removal of toxic vanillin from the medium by XAD-2 resin absorption. The vanillin production of NTG-VR1 increased to three times at 5 g/L of ferulic acid when compared with its wild-type strain. When 50% (w/v) of XAD-2 resin was employed in culture with 10 g/L of ferulic acid, the vanillin production of NTG-VR1 was 2.9 g/L, which was 2-fold higher than that obtained with no use of the resin.

  4. Experimental data developed to support the selection of a treatment process for West Valley alkaline supernatant

    Energy Technology Data Exchange (ETDEWEB)

    Bray, L.A.; Holton, L.K.; Myers, T.R.; Richardson, G.M.; Wise, B.M.

    1984-01-01

    At the request of West Valley Nuclear Services Co., Inc., the Pacific Northwest Laboratory (PNL) has studied alternative treatment processes for the alkaline PUREX waste presently being stored in Tank 8D2 at West Valley, New York. Five tasks were completed during FY 1983: (1) simulation and characterization of the alkaline supernatant and sludge from the tank. The radiochemical and chemical distributions between the aqueous and solid phase were determined, and the efficiency of washing sludge with water to remove ions such as Na/sup +/ and SO/sub 4//sup 2 -/ was investigated; (2) evaluation of a sodium tetraphenylboron (Na-TPB) precipitation process to recover cesium (Cs) and a sodium titanate (Na-TiA) sorption process to recover strontium (Sr) and plutonium (Pu) from the West Valley Alkaline supernatant. These processes were previously developed and tested at the US Department of Energy's Savannah River Plant; (3) evaluation of an organic cation-exchange resin (Duolite CS-100) to recover Cs and Pu from the alkaline supernatant followed by an organic macroreticular cation exchange resin (Amberlite IRC-718) to recover Sr; (4) evaluation of an inorganic ion exchanger (Linde Ionsiv IE-95) to recover Cs, Sr, and Pu from the alkaline supernatant; and (5) evaluation of Dowex-1,X8 organic anion exchange resin to recover technetium (Tc) from alkaline supernatant. The findings of these tasks are reported. 21 references, 36 figures, 34 tables.

  5. Origin of the strain glass transition in Ti_5_0(Ni_5_0_−_x D_x) alloys

    International Nuclear Information System (INIS)

    Wang, Xu; Shang, Jia-Xiang; Wang, Fu-He; Chen, Yue

    2016-01-01

    Direct evidence was recently discovered for the unique strain glass (STG) transition, which breaks the local symmetries (PRL 112, 025701 (2014)). To understand the origin of the STG transition, the effects of doping point defects on Ti_5_0(Ni_5_0_−_x D_x) are investigated using first-principle calculations. The experimental observation that STG only exists in a limited range of chemical composition x is successfully rationalized. The mechanisms that correspond to the division of a system into domains with distinctly different compositions are found to be directly related to a dip in the defect formation energy. - Highlights: • The strain glass transition phenomenon in Ti−Ni-based alloys is rationalized. • The electronic-structure origins of the strain glass transition are uncovered. • The separation of domains with different compositions is explained.

  6. Surface discoloration of composite resins: Effects of staining and bleaching.

    Science.gov (United States)

    Poggio, Claudio; Beltrami, Riccardo; Scribante, Andrea; Colombo, Marco; Chiesa, Marco

    2012-09-01

    The purpose of this in vitro study was to evaluate surface discoloration of three microhybrid composite resins (Esthet•X HD, Clearfil AP-X, Gradia Direct) and five nanohybrid composite resins (Ceram•X, GC Kalore, G-aenial, Grandio, GrandioSO), after staining and bleaching procedures. The composite resins were polymerized with a curing light (Celalux II, Voco, Cuxhaven, Germany) into 160 silicon molds (6,4 mm in diameter and 2 mm in thickness) to obtain identical specimens. Twenty samples for each composite resin were prepared. The specimens were polished using an automated polishing machine with the sequence of 600-, 800-, 1000-grit abrasive paper under water irrigation. The specimens were immersed in tea and distilled water: the specimens were dipped for 20 min, once a day (every 24 h), for 14 days into the drinks. The specimens were then bleached with carbamide peroxide at 17% (Perfect Bleach-Voco). The color of specimens was measured with a spectrophotometer according to the CIE L(*)a(*)b(*) system after light-polymerization of composite resin specimens, after 7 days, after 14 days, and after bleaching. The color difference h index (DEab(*)) between each measurement was calculated. Statistical analysis was made using analysis of variance (ANOVA). All specimens showed a significant increase in staining with a similar trend and no significant differences between microhybrid and nanohybrid composite resins. After whitening procedures, materials tested showed both significant and unsignificant differences of the h index. Microhybrid and nanohybrid composite resins had similar in vitro surface discoloration in tea. After bleaching, discoloration was removed from some composite resins tested.

  7. Assessment of surface hardness of acrylic resins submitted to accelerated artificial aging.

    Science.gov (United States)

    Tornavoi, D C; Agnelli, J A M; Lepri, C P; Mazzetto, M O; Botelho, A L; Soares, R G; Dos Reis, A C

    2012-06-01

    The aim of this study was to assess the influence of accelerated artificial aging (AAA) on the surface hardness of acrylic resins. The following three commercial brands of acrylic resins were tested: Vipi Flash (autopolymerized resin), Vipi Wave (microwave heat-polymerized resin) and Vipi Cril (conventional heat-polymerized resin). To perform the tests, 21 test specimens (65x10x3 mm) were made, 7 for each resin. Three surface hardness readings were performed for each test specimen, before and after AAA, and the means were submitted to the following tests: Kolmogorov-Smirnov (P>0.05), Levene Statistic, Two-way ANOVA, Tukey Post Hoc (Paging, the autopolymerized acrylic resin Vipi Flash showed lower hardness values when compared with the heat-polymerized resin Vipi Cril (P=0.001). After aging, the 3 materials showed similar performance when compared among them. The Vipi Cril was the only one affected by AAA and showed lower hardness values after this procedure (Pp=0.003). It may be concluded that accelerated artificial aging influenced surface hardness of heat-polymerized acrylic resin Vipi Cril.

  8. Recent progress of hard x-ray imaging microscopy and microtomography at BL37XU of SPring-8

    Energy Technology Data Exchange (ETDEWEB)

    Suzuki, Yoshio, E-mail: yoshio@spring8.or.jp; Takeuchi, Akihisa; Terada, Yasuko; Uesugi, Kentaro [Japan Synchrotron Radiation Research Institute (JASRI/SPring-8), Sayo, Hyogo 679-5198 (Japan); Mizutani, Ryuta [Department of Applied Biochemistry, Tokai University, Hiratsuka, Kanagawa 259-1292 (Japan)

    2016-01-28

    A hard x-ray imaging microscopy and microtomography system is now being developed at the beamline 37XU of SPring-8. In the latest improvement, a spatial resolution of about 50 nm is achieved in two-dimensional imaging at 6 keV x-ray energy using a Fresnel zone plate objective with an outermost zone width of 35 nm. In the tomographic measurement, a spatial resolution of about 100 nm is achieved at 8 keV using an x-ray guide tube condenser optic and a Fresnel zone plate objective with an outermost zone width of 50 nm.

  9. Multimode-singlemode-multimode optical fiber sensor coated with novolac resin for detecting liquid phase alcohol

    Science.gov (United States)

    Marfu'ah, Amalia, Niza Rosyda; Hatta, Agus Muhamad; Pratama, Detak Yan

    2018-04-01

    Alcohol sensor based on multimode-singlemode-multimode (MSM) optical fiber with novolac resin as the external medium is proposed and demonstrated experimentally. Novolac resin swells when it is exposed by the alcohol. This effect causes a change in the polymer density leading to the refractive index's variation. The transmission light of the sensor depends on the refractive index of external medium. Based on the results, alcohol sensor based on MSM optical fiber structure using novolac resin has a higher sensitivity compared to the sensor without using novolac resin in the mixture of alcohol and distilled water. Alcohol sensor based on MSM optical fiber structure using novolac resin in the mixture of alcohol and distilled water with a singlemode fiber length of 5 mm has a sensitivity of 0.028972 dBm per % V/V, and in the mixture of alcohol and sugar solution of 10% w/w has a sensitivity of 0.005005 dBm per % V/V.

  10. Fabrication of 5 cm long epitaxial Sm{sub 0.2}Ce{sub 0.8}O{sub 1.9-x} single buffer layer on textured Ni-5%W substrate for YBCO coated conductors via dip-coating PACSD method

    Energy Technology Data Exchange (ETDEWEB)

    Lei, M.; Wang, W.T.; Pu, M.H.; Yang, X.S.; He, L.J. [Key Laboratory of Magnetic Levitation and Maglev Trains (Ministry of Education of China), Superconductivity R and D Center (SRDC), Mail Stop 165, Southwest Jiaotong University, Chengdu, Sichuan 610031 (China); Cheng, C.H. [Science and Engineering, University of New South Wales, Sydney 2052, New South Wales (Australia); Zhao, Y., E-mail: yzhao@home.swjtu.edu.cn [Key Laboratory of Magnetic Levitation and Maglev Trains (Ministry of Education of China), Superconductivity R and D Center (SRDC), Mail Stop 165, Southwest Jiaotong University, Chengdu, Sichuan 610031 (China)] [Science and Engineering, University of New South Wales, Sydney 2052, New South Wales (Australia)

    2011-11-15

    Epitaxial Sm{sub 0.2}Ce{sub 0.8}O{sub 1.9-x} single buffer layer for YBCO coated conductors was deposited via fluorine-free dip-coating CSD. Flat, dense and crack-free SCO films with sharp (2 0 0) c-axis texture were obtained by carefully controlling the processing. YBCO thin films with a homogeneous surface microstructure were deposited on the SCO-buffered NiW substrate via CSD approach. Five centimeters long epitaxial Sm{sub 0.2}Ce{sub 0.8}O{sub 1.9-x} (SCO) single buffer layer for YBCO coated conductors was deposited via dip-coating polymer-assisted chemical solution deposition (PACSD) approach on bi-axially textured Ni-5%W (2 0 0) alloy substrate. The film formation and texture evolution were investigated using X-ray diffraction and scanning electron microscopy. Flat, dense and crack-free SCO films with sharp (2 0 0) c-axis texture were obtained by way of carefully controlling the concentration of precursor solution, withdrawing speed, annealing temperature and dwelling time. On consideration of both microstructure and texture, epitaxial SCO single buffer layers were fabricated using precursor solution of 0.3 M cationic concentration, the withdrawing speed of 10 mm/min and heat treatment at 1100 deg. C in Ar-5%H{sub 2} mixture gas for 0.5 h. Epitaxial YBCO thin films with a homogeneous surface microstructure were deposited on the SCO-buffered NiW substrate via dip-coating PACSD approach. The PACSD approach was a promising way to fabricate long and low-cost YBCO coated conductors.

  11. High-temperature reactivity in the ZrW2O8-Cu system

    International Nuclear Information System (INIS)

    Verdon, C.; Dunand, D.C.

    1997-01-01

    Zirconium tungstate (ZrW 2 O 8 ) exhibits the unusual property of a negative coefficient of thermal expansion (CTE) over a wide range of temperature, from 0.3 to 1,050 K. As a reinforcement in a composite, zirconium tungstate can reduce the overall thermal expansion of the composite much more effectively than a ceramic with positive CTE. If a metallic matrix is used, the resulting composite will also exhibit high thermal conductivity, with applications such as heat sink for microelectronics devices (CTE matching that of silicon or alumina) or high precision optical elements subjected to thermal fluctuation (zero CTE). As a matrix, copper is prime candidate, because it has the second highest thermal conductivity of all metals after silver, and because it can be easily processed within the temperature window imposed by the metastability of ZrW 2 O 8 . Moreover, copper is already widely used in electronics industry and can be easily soldered. In the present work, the authors investigate the stability of ZrW 2 O 8 when hot-isostatically pressed with copper, in order to explore the processing feasibility of a low thermal expansion, high conductivity ZrW 2 O 8 -Cu composite

  12. Ternary scandium-rich indides Sc{sub 50}T{sub 13}In{sub 3} and Sc{sub 50}Rh{sub 13}In{sub 3}O{sub y} (T = Rh, Ir; y {approx} 8) - synthesis and crystal structure

    Energy Technology Data Exchange (ETDEWEB)

    Zaremba, R.; Poettgen, R. [Inst. fuer Anorganische und Analytische Chemie, Univ. Muenster (Germany)

    2007-12-15

    New intermetallic compounds Sc{sub 50}Rh{sub 13.3}In{sub 2.7} and Sc{sub 50}Ir{sub 13.6}In{sub 2.4} and the suboxides Sc{sub 49.2}Rh{sub 13}In{sub 3.8}O{sub 8.8} and Sc{sub 49.2}Rh{sub 13.7}In{sub 2.8}O{sub 8.0} were synthesized from the elements or with Sc{sub 2}O{sub 3} as an oxygen source, respectively, in sealed tantalum tubes in a water-cooled sample chamber of an induction furnace. They crystallize with a new cubic structure type, space group F m anti 3, a = 1772.5(6) pm, wR2 = 0.032, 1111 F{sup 2} values, 34 variables for Sc{sub 50}Rh{sub 13.3}In{sub 2.7}, a = 1766.5(6) pm, wR2 = 0.041, 745 F{sup 2} values, 34 variables for Sc{sub 50}Ir{sub 13.6}In{sub 2.4}, a = 1764.4(2) pm, wR2 = 0.044, 640 F{sup 2} values, 41 variables for Sc{sub 49.2}Rh{sub 13}In{sub 3.8}O{sub 8.8}, and a = 1761.5(6) pm, wR2 = 0.054, 740 F{sup 2} values, 42 variables for Sc{sub 49.2}Rh{sub 13.7}In{sub 2.8}O{sub 8.0}. The main structural motifs are rhodium-centered indium cubes in an fcc like arrangement in which the octahedral and tetrahedral voids are filled by In2Sc{sub 12} and In1Sc{sub 12} icosahedra, respectively, resembling a Li{sub 3}Bi-like structure. The Rh1 (Ir1) and Sc4 atoms lie between these polyhedral units. The oxygen atoms partially fill Sc{sub 6} octahedra in Sc{sub 49.2}Rh{sub 13}In{sub 3.8}O{sub 8.8} and Sc{sub 49.2}Rh{sub 13.7}In{sub 2.8}O{sub 8.0} with Sc-O distances of 214 - 230 pm. These octahedra are condensed via common edges and faces, encapsulating the In2Sc{sub 12} icosahedra. Due to the high scandium content one observes strong Sc-Sc bonding with Sc-Sc distances ranging from 303 to 362 pm in Sc{sub 49.2}Rh{sub 13}In{sub 3.8}O{sub 8.8}. The shortest distances occur for Sc-Rh (267 - 295 pm). The crystal chemical relationship with the Li{sub 3}Bi-related suboxide Ti{sub 12}Sn{sub 3}O{sub 10} is discussed. (orig.)

  13. Evaluation of resins for use in brachytherapy

    Energy Technology Data Exchange (ETDEWEB)

    Carvalho, Luiz Claudio F.M. Garcia; Ferraz, Wilmar Barbosa; Chrcanovic, Bruno Ramos; Santos, Ana Maria M., E-mail: ferrazw@cdtn.b, E-mail: amms@cdtn.b [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil)

    2011-07-01

    Brachytherapy is an advanced cancer treatment where radioactive seeds or sources are placed near or directly into the tumor thus reducing the radiation exposure in the surrounding healthy tissues. Prostate cancer can be treated with interstitial brachytherapy in initial stage of the disease in which tiny radioactive seeds with cylindrical geometry are used. Several kinds of seeds have been developed in order to obtain a better dose distribution around them and with a lower cost manufacturing. These seeds consist of an encapsulation, a radionuclide carrier, and X-ray marker. Among the materials that have potential for innovation in the construction of seeds, biocompatible resins appear as an important option. In this paper, we present some characterization results with Fourier transform infrared spectroscopic (FTIR) and ultraviolet-visible spectroscopy (UV-vis) performed on two types of resins in which curing temperatures for each one were varied as also the results of coatings with these resins under titanium substrates. Interactions of these resins in contact with the simulated body fluid were evaluated by atomic force microscopy, scanning electron microscopy, and energy dispersive X-ray spectroscopy. (author)

  14. Moessbauer studies of the LiAl sub(5-x) Fe sub(x) O8 and LiGa sub(5-x) Fe sub(x) O8 systems

    International Nuclear Information System (INIS)

    Barthem, V.M.T.S.; Maria Neto, J.; Souza Barros, F. de

    1982-01-01

    Comparative Moessbauer studies of the LiGa sub(5-x) Fe sub(x) O 8 and LiAl sub(5-x) Fe sub(x) O 8 systems are shown. The characteristics of the Moessbauer spectra, obtained with LiGa 5 O 8 samples with 0,1% of Fe 3+ , differ drastically from that observed with LiAl 5 O 8 with the same three-valent iron concentration. All these differences are related to the more covalent character of the gallium-oxygen binding, when compared with the aluminium-oxygen one. (L.C.) [pt

  15. Fabrication of low thermal expansion SiC/ZrW{sub 2}O{sub 8} porous ceramics

    Energy Technology Data Exchange (ETDEWEB)

    Poowancum, A; Matsumaru, K; Juarez-Ramirez, I; Ishizaki, K [Department of Mechanical Engineering, Nagaoka University of Technology, 1603-1 Kamitomioka, Nagaoka, Niigata 940-2188 (Japan); Torres-Martinez, L M [Universidad Autonoma de Nuevo Leon, Av. Universidad s/n, San Nicolas de los Garza, NL, C.P. 66451 (Mexico); Fu, Z Y [State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan, Hubei, 430070 (China); Lee, S W, E-mail: anurat@ishizaki.nagaokaut.ac.jp [Department of Environment Engineering, Sun Moon University, 100, Kalsan-ri, Tangjeong-myeon, Asan, Chungnam 336-708 (Korea, Republic of)

    2011-03-15

    Low or zero thermal expansion porous ceramics are required for several applications. In this work near zero thermal expansion porous ceramics were fabricated by using SiC and ZrW{sub 2}O{sub 8} as positive and negative thermal expansion materials, respectively, bonded by soda lime glass. The mixture of SiC, ZrW{sub 2}O{sub 8} and soda lime glass was sintered by Pulsed Electric Current Sintering (PECS, or sometimes called Spark Plasma Sintering, SPS) at 700 deg. C. Sintered samples with ZrW{sub 2}O{sub 8} particle size smaller than 25 {mu}m have high thermal expansion coefficient, because ZrW{sub 2}O{sub 8} has the reaction with soda lime glass to form Na{sub 2}ZrW{sub 3}O{sub 12} during sintering process. The reaction between soda lime glass and ZrW{sub 2}O{sub 8} is reduced by increasing particle size of ZrW{sub 2}O{sub 8}. Sintered sample with ZrW{sub 2}O{sub 8} particle size 45-90 {mu}m shows near zero thermal expansion.

  16. Utility of solid phase spectrophotometry for the modified determination of trace amounts of cadmium in food samples.

    Science.gov (United States)

    Amin, Alaa S; Gouda, Ayman A

    2012-05-01

    A modified selective, highly sensitive and accurate procedure for the determination of trace amounts of cadmium which reacts with 1-(2-benzothiazolylazo)-2-hydroxy-3-naphthoic acid (BTAHNA) to give a deep violet complex with high molar absorptivity (7.05×10(6)Lmol(-1) cm(-1), 3.92×10(7)Lmol(-1)cm(-1), 1.78×10(8)Lmol(-1)cm(-1), and 4.10×10(8)Lmol(-1)cm(-1)), fixed on a Dowex 1-X8 type anion-exchange resin for 10mL, 100mL, 500mL, and 1000mL, respectively. Calibration is linear over the range 0.2-3.5μgL(-1) with RSD of ⩽1.14% (n=10). The detection and quantification limits were calculated. Increasing the sample volume can enhance the sensitivity. The method has been successfully applied for the determination of Cd(II) in food samples, water samples and some salts samples without interfering effect of various cations and anions. Copyright © 2011 Elsevier Ltd. All rights reserved.

  17. A50-kW(el) solar energy thermionic power generator for spacecraft

    International Nuclear Information System (INIS)

    Sahin, S.

    1978-01-01

    The technical limits of thermionic reactors in space craft and the potentials of solar energy thermionic converters are discussed. The technical design of a solar energy thermionic generator for 50 kW(el) as a secondary energy source in unmanned space craft is presented. (GG) [de

  18. Resin-modified and conventional glass ionomer restorations in primary teeth: 8-year results

    DEFF Research Database (Denmark)

    Qvist, V.; Manscher, E.; Teglers, P.T.

    2004-01-01

    clinical trial, cariostatic effects, dental restorations, glass ionomer cement, long-term behaviour, pedodontics, resin-modified glass ionomer......clinical trial, cariostatic effects, dental restorations, glass ionomer cement, long-term behaviour, pedodontics, resin-modified glass ionomer...

  19. Silica-supported tungsten carbynes (≡SiO)xW(≡CH)(Me)y (x = 1, y = 2; X = 2, y = 1): New efficient catalysts for alkyne cyclotrimerization

    KAUST Repository

    Riache, Nassima

    2015-02-23

    The activity of silica-supported tungsten carbyne complexes (≡SiO)xW(≡CH)(Me)y (x = 1, y = 2; x = 2, y = 1) toward alkynes is reported. We found that they are efficient precatalysts for terminal alkyne cyclotrimerization with high TONs. We also demonstrate that this catalyst species is active for alkyne cyclotrimerization without the formation of significant alkyne metathesis products. Additional DFT calculations highlight the importance of the W coordination sphere in supporting this experimental behavior.

  20. Single top quark t W + X production at the LHC a closer look

    CERN Document Server

    Belyaev, A.

    2001-01-01

    We have reexamined the tW+X single top-quark production process which is important at the LHC contrary to the Tevatron. The special attention was paid to the treatment of the 2->2[Wt] process and the part of it's next-to-leading correction: 2->3[Wtb] process. We show that 2->3[Wtb] process has to be correctly taken into account with a proper subtraction of the top pair contribution and that it has qualitatively different kinematical distributions from the 2->2[Wt] process. We present the total cross section of the tW+X production to be about 62 pb at QCD scale be taken as a top quark mass, suggest the method of combining Wt and Wtb processes with gauge invariant subtraction of the tt-bar part which allows to reproduce correct kinematical properties and perform a proper event simulation of the tW+X process in the whole kinematical region.

  1. Search for triboson W{sup ±}W{sup ±}W{sup -+} production in pp collisions at √(s) = 8 TeV with the ATLAS detector

    Energy Technology Data Exchange (ETDEWEB)

    Aaboud, M. [Univ. Mohamed Premier et LPTPM, Oujda (Morocco). Faculte des Sciences; Aad, G. [CPPM, Aix-Marseille Univ. et CNRS/IN2P3, Marseille (France); Abbott, B. [Oklahoma Univ., Norman, OK (United States). Homer L. Dodge Dept. of Physics and Astronomy; Collaboration: ATLAS Collaboration; and others

    2017-03-15

    This paper reports a search for triboson W{sup ±}W{sup ±}W{sup -+} production in two decay channels (W{sup ±}W{sup ±}W{sup -+} → l{sup ±}νl{sup ±}νl{sup -+}ν and W{sup ±}W{sup ±}W{sup -+} → l{sup ±}νl{sup ±}νjj with l = e, μ) in proton-proton collision data corresponding to an integrated luminosity of 20.3 fb{sup -1} at a centre-of-mass energy of 8 TeV with the ATLAS detector at the Large Hadron Collider. Events with exactly three charged leptons, or two leptons with the same electric charge in association with two jets, are selected. The total number of events observed in data is consistent with the Standard Model (SM) predictions. The observed 95% confidence level upper limit on the SM W{sup ±}W{sup ±}W{sup -+} production cross section is found to be 730 fb with an expected limit of 560 fb in the absence of SM W{sup ±}W{sup ±}W{sup -+} production. Limits are also set on WWWW anomalous quartic gauge couplings. (orig.)

  2. Lessons learned from the manufacture of the W7-X planar coils

    Science.gov (United States)

    Viebke, H.; Gustke, D.; Rummel, T.; Sborchia, C.; Schroeder, R.; Williams, D.; Bates, S.; Leigh, B.; Winter, R.

    2006-06-01

    WENDELSTEIN 7-X (W7-X) is a superconducting stellarator. The planar coils are in charge to modify the magnetic filed configuration of the W7-X. The major challenges during manufacturing were the fabrication of the cable-in-conduit conductor, the accuracy of the coil cases after welding and machining and the development of electrical joints with a resistance below 1 nΩ. Leaks were detected during repetitive in the case cooling system, which were caused by stress corrosion cracking. High voltage tests in a reduced vacuum environment (Paschen conditions) revealed that the insulation had to be reinforced and the quench detection wires had to be exchanged. This paper gives an overview about the main technical challenges of the planar coils and the lessons learned during production.

  3. Lessons learned from the manufacture of the W7-X planar coils

    International Nuclear Information System (INIS)

    Viebke, H; Gustke, D; Rummel, T; Sborchia, C; Schroeder, R; Williams, D; Bates, S; Leigh, B; Winter, R

    2006-01-01

    WENDELSTEIN 7-X (W7-X) is a superconducting stellarator. The planar coils are in charge to modify the magnetic filed configuration of the W7-X. The major challenges during manufacturing were the fabrication of the cable-in-conduit conductor, the accuracy of the coil cases after welding and machining and the development of electrical joints with a resistance below 1 nΩ. Leaks were detected during repetitive in the case cooling system, which were caused by stress corrosion cracking. High voltage tests in a reduced vacuum environment (Paschen conditions) revealed that the insulation had to be reinforced and the quench detection wires had to be exchanged. This paper gives an overview about the main technical challenges of the planar coils and the lessons learned during production

  4. Nanoindentation creep versus bulk compressive creep of dental resin-composites.

    Science.gov (United States)

    El-Safty, S; Silikas, N; Akhtar, R; Watts, D C

    2012-11-01

    To evaluate nanoindentation as an experimental tool for characterizing the viscoelastic time-dependent creep of resin-composites and to compare the resulting parameters with those obtained by bulk compressive creep. Ten dental resin-composites: five conventional, three bulk-fill and two flowable were investigated using both nanoindentation creep and bulk compressive creep methods. For nano creep, disc specimens (15mm×2mm) were prepared from each material by first injecting the resin-composite paste into metallic molds. Specimens were irradiated from top and bottom surfaces in multiple overlapping points to ensure optimal polymerization using a visible light curing unit with output irradiance of 650mW/cm(2). Specimens then were mounted in 3cm diameter phenolic ring forms and embedded in a self-curing polystyrene resin. Following grinding and polishing, specimens were stored in distilled water at 37°C for 24h. Using an Agilent Technologies XP nanoindenter equipped with a Berkovich diamond tip (100nm radius), the nano creep was measured at a maximum load of 10mN and the creep recovery was determined when each specimen was unloaded to 1mN. For bulk compressive creep, stainless steel split molds (4mm×6mm) were used to prepare cylindrical specimens which were thoroughly irradiated at 650mW/cm(2) from multiple directions and stored in distilled water at 37°C for 24h. Specimens were loaded (20MPa) for 2h and unloaded for 2h. One-way ANOVA, Levene's test for homogeneity of variance and the Bonferroni post hoc test (all at p≤0.05), plus regression plots, were used for statistical analysis. Dependent on the type of resin-composite material and the loading/unloading parameters, nanoindentation creep ranged from 29.58nm to 90.99nm and permanent set ranged from 8.96nm to 30.65nm. Bulk compressive creep ranged from 0.47% to 1.24% and permanent set ranged from 0.09% to 0.38%. There was a significant (p=0.001) strong positive non-linear correlation (r(2)=0.97) between bulk

  5. Investigation of the magnetic phase transition in thin Fe{sub 50}Pt{sub 50-x}Rh{sub x} films by neutron diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Fenske, Jochen; Lott, Dieter; Schreyer, Andreas [GKSS Research Centre, Geesthacht (Germany); Mankey, Gary J. [MINT Center, The University of Alabama, Tuscaloosa, AL (United States); Schmidt, Wolfgang; Schmalzl, Karin [JCNS, Juelich (Germany)

    2008-07-01

    In the last years perpendicular recording plays a major role in the development of novel magnetic data storage. Here, materials with high anisotropy are used which delivers good thermal stability. However in order to write the bits a high magnetic field is necessary. By the use of soft underlayers the write field can be significant reduced. Fe{sub 50}Pt{sub 50-x}Rh{sub x} is a promising candidate for such an underlayer. Magnetization measurements of the bulk samples for x=10 refer to a antiferromagnetic (AF)/ferromagnetic (FM) phase transition at about 150 K when heated. Additional magnetostriction measurements indicate that the phase transition could also be induced by applying a magnetic field. The FM state lowers the high anisotropy and therefore the high write field. The AF state helps to stabilize the recording media via exchange interaction. For technical applications the use of thin films are essential to save space and costs for the next generation of magnetic storage devices. Here we present results on several thin Fe{sub 50}Pt{sub 50-x}Rh{sub x} films with different concentration of Rh. The films were examined by polarized and unpolarized neutron diffraction in dependence of temperature and magnetic field.

  6. Investigation of Radioiodination of Meta-Iodobenzylguanidine Compound with 131I Isotope in Solid Phase Using Cu Catalyzer

    International Nuclear Information System (INIS)

    Davarpanah, M. R.; Attar Nosrati, S.; Khoshhosn, H.; Kazemi Boudani, M.; Fazlali, M.; Ghannadi Maragheh, M.

    2012-01-01

    In this study the radioiodination process of meta-iodobenzylguanidine with 131 I isotope in presence of ammonium sulphate and Cu(II) Catalyzer was investigated. In order to optimize the process, the influence of different parameters on labeling yield was studied. The results of experiments showed that the use of oil bath with temperature of 160 d egree C is necessary. After the labeling process, purification step of the final product was carried out using Dowex-1 x 8 resin. The mean labeling yield was 97.2 p ercent . In this method radiolabelling of MIBG with 131 I (185 MBq for diagnostic dose and 3330 MBq for therapeutic dose) is quite simple and it complies with the requirements of routine production of 13 1I-MIBG radiopharmaceutical for diagnostic and therapeutic purposes. This paper is a narration of industrial scale production of 131 I-MIBG radiopharmaceutical.

  7. Design of multichannel laser interferometry for W7-X

    International Nuclear Information System (INIS)

    Kornejew, P.; Hirsch, M.; Bindemann, T.; Dinklage, A.; Dreier, H.; Hartfuss, H.-J.

    2006-01-01

    An eight channel interferometer is developed for density feedback control and the continuous measurement of electron density profiles in the stellarator W7-X. An additional sightline is launched in the geometry of the Thomson scattering for cross calibration. Due to the W7-X coil geometry access is strongly restricted. This motivates the optimization of the sightline geometry and design studies for supplementary chords. In-vessel retroreflectors will be used and inserted in the first wall elements. To cope with associated mechanical vibrations and thermal drifts during the discharges with envisaged duration of 30 min either two-color or second harmonic interferometry techniques must be applied. Optimum wavelengths are found to be about 10 and 5 μm. A CO 2 /CO interferometer (10 μm/5 μm) will be tested and compared with an existing CO 2 /HeNe test interferometer. A special difficulty of remotely operated diagnostics is the need of long transmission lines with a path length of about 60 m required from the diagnostics location to the torus hall and back. Different arrangements will be compared

  8. Determination of vanadium in sea water by graphite furnace atomic absorption spectrometry with a tube coated with pyrolytic graphite

    International Nuclear Information System (INIS)

    Shimizu, Tokuo; Sakai, Kaoru

    1981-01-01

    The trace amount of vanadium in sea water was determined by graphite furnace atomic absorption spectrometry with a tube coated with pyrolytic graphite. To correct the background absorption, a deuterium lamp with a higher-brilliant thermal cathode was used. The sensitivity for vanadium increased 10 -- 20 fold by the use of the tube coated with pyrolytic graphite, and the utility lifetime of the tube was greatly extended. Vanadium(V) - 4-(2-pyridylazo)resorcinol (PAR) complexes were extracted into chloroform as an ion-pair with benzyldimethyltetradecylammonium (Zephiramine) cation alternatively. The sample of sea water, which was made to 0.1 N in sulfuric acid and 0.1% in hydrogen peroxide, was loaded onto the column of Dowex 1-X 4 resin (SO 4 2- -form). Vanadium was then eluted from the resin with 1 N sulfuric acid-0.1% hydrogen peroxide or 1 N hydrochloric acid-0.1% hydrogen peroxide evaporated to dry. After dissolution of the elute in 0.2 N nitric acid, vanadium was extracted. Secondly, the sample of sea water was adjusted to pH 5.0, and loaded onto the column of Chelex-100 resin. Vanadium was eluted from the resin with 2 N ammonia. The above two methods took much time, but the coprecipitation method was not so and recommended for the determination of vanadium in sea water. Vanadium was coprecipitated with iron(III) hydroxide-hydrous titanium(IV) oxide at pH 6.0. The precipitate was digested with nitric acid-hydrogen peroxide. The solution was diluted to 50 ml with water. The resulting solutions were employed to determine the vanadium concentration by the graphite furnace atomic absorption measurement. The trace amounts of vanadium in various kinds of the coastal sea water were determined by the coprecipitation method. (author)

  9. Colour reconnection studies in $e^{+}e^{-} \\to W^{+}W^{-}$ at $\\sqrt{s}$=183 GeV

    CERN Document Server

    Abbiendi, G.; Alexander, G.; Allison, John; Altekamp, N.; Anderson, K.J.; Anderson, S.; Arcelli, S.; Asai, S.; Ashby, S.F.; Axen, D.; Azuelos, G.; Ball, A.H.; Barberio, E.; Barlow, Roger J.; Bartoldus, R.; Batley, J.R.; Baumann, S.; Bechtluft, J.; Behnke, T.; Bell, Kenneth Watson; Bella, G.; Bellerive, A.; Bentvelsen, S.; Bethke, S.; Betts, S.; Biebel, O.; Biguzzi, A.; Bird, S.D.; Blobel, V.; Bloodworth, I.J.; Bock, P.; Bohme, J.; Bonacorsi, D.; Boutemeur, M.; Braibant, S.; Bright-Thomas, P.; Brigliadori, L.; Brown, Robert M.; Burckhart, H.J.; Capiluppi, P.; Carnegie, R.K.; Carter, A.A.; Carter, J.R.; Chang, C.Y.; Charlton, David G.; Chrisman, D.; Ciocca, C.; Clarke, P.E.L.; Clay, E.; Cohen, I.; Conboy, J.E.; Cooke, O.C.; Couyoumtzelis, C.; Coxe, R.L.; Cuffiani, M.; Dado, S.; Dallavalle, G.Marco; Davis, R.; De Jong, S.; de Roeck, A.; Dervan, P.; Desch, K.; Dienes, B.; Dixit, M.S.; Dubbert, J.; Duchovni, E.; Duckeck, G.; Duerdoth, I.P.; Eatough, D.; Estabrooks, P.G.; Etzion, E.; Fabbri, F.; Fanti, M.; Faust, A.A.; Fiedler, F.; Fierro, M.; Fleck, I.; Folman, R.; Furtjes, A.; Futyan, D.I.; Gagnon, P.; Gary, J.W.; Gascon, J.; Gascon-Shotkin, S.M.; Gaycken, G.; Geich-Gimbel, C.; Giacomelli, G.; Giacomelli, P.; Gibson, V.; Gibson, W.R.; Gingrich, D.M.; Glenzinski, D.; Goldberg, J.; Gorn, W.; Grandi, C.; Graham, K.; Gross, E.; Grunhaus, J.; Gruwe, M.; Hanson, G.G.; Hansroul, M.; Hapke, M.; Harder, K.; Harel, A.; Hargrove, C.K.; Hartmann, C.; Hauschild, M.; Hawkes, C.M.; Hawkings, R.; Hemingway, R.J.; Herndon, M.; Herten, G.; Heuer, R.D.; Hildreth, M.D.; Hill, J.C.; Hobson, P.R.; Hoch, M.; Hocker, James Andrew; Hoffman, Kara Dion; Homer, R.J.; Honma, A.K.; Horvath, D.; Hossain, K.R.; Howard, R.; Huntemeyer, P.; Igo-Kemenes, P.; Imrie, D.C.; Ishii, K.; Jacob, F.R.; Jawahery, A.; Jeremie, H.; Jimack, M.; Jones, C.R.; Jovanovic, P.; Junk, T.R.; Karlen, D.; Kartvelishvili, V.; Kawagoe, K.; Kawamoto, T.; Kayal, P.I.; Keeler, R.K.; Kellogg, R.G.; Kennedy, B.W.; Kim, D.H.; Klier, A.; Kluth, S.; Kobayashi, T.; Kobel, M.; Koetke, D.S.; Kokott, T.P.; Kolrep, M.; Komamiya, S.; Kowalewski, Robert V.; Kress, T.; Krieger, P.; von Krogh, J.; Kuhl, T.; Kyberd, P.; Lafferty, G.D.; Landsman, H.; Lanske, D.; Lauber, J.; Lautenschlager, S.R.; Lawson, I.; Layter, J.G.; Lazic, D.; Lee, A.M.; Lellouch, D.; Letts, J.; Levinson, L.; Liebisch, R.; List, B.; Littlewood, C.; Lloyd, A.W.; Lloyd, S.L.; Loebinger, F.K.; Long, G.D.; Losty, M.J.; Ludwig, J.; Lui, D.; Macchiolo, A.; Macpherson, A.; Mader, W.; Mannelli, M.; Marcellini, S.; Markopoulos, C.; Martin, A.J.; Martin, J.P.; Martinez, G.; Mashimo, T.; Mattig, Peter; McDonald, W.John; McKenna, J.; Mckigney, E.A.; McMahon, T.J.; McPherson, R.A.; Meijers, F.; Menke, S.; Merritt, F.S.; Mes, H.; Meyer, J.; Michelini, A.; Mihara, S.; Mikenberg, G.; Miller, D.J.; Mir, R.; Mohr, W.; Montanari, A.; Mori, T.; Nagai, K.; Nakamura, I.; Neal, H.A.; Nellen, B.; Nisius, R.; O'Neale, S.W.; Oakham, F.G.; Odorici, F.; Ogren, H.O.; Oreglia, M.J.; Orito, S.; Palinkas, J.; Pasztor, G.; Pater, J.R.; Patrick, G.N.; Patt, J.; Perez-Ochoa, R.; Petzold, S.; Pfeifenschneider, P.; Pilcher, J.E.; Pinfold, J.; Plane, David E.; Poffenberger, P.; Polok, J.; Przybycien, M.; Rembser, C.; Rick, H.; Robertson, S.; Robins, S.A.; Rodning, N.; Roney, J.M.; Roscoe, K.; Rossi, A.M.; Rozen, Y.; Runge, K.; Runolfsson, O.; Rust, D.R.; Sachs, K.; Saeki, T.; Sahr, O.; Sang, W.M.; Sarkisian, E.K.G.; Sbarra, C.; Schaile, A.D.; Schaile, O.; Scharf, F.; Scharff-Hansen, P.; Schieck, J.; Schmitt, B.; Schmitt, S.; Schoning, A.; Schroder, Matthias; Schumacher, M.; Schwick, C.; Scott, W.G.; Seuster, R.; Shears, T.G.; Shen, B.C.; Shepherd-Themistocleous, C.H.; Sherwood, P.; Siroli, G.P.; Sittler, A.; Skuja, A.; Smith, A.M.; Snow, G.A.; Sobie, R.; Soldner-Rembold, S.; Spagnolo, S.; Sproston, M.; Stahl, A.; Stephens, K.; Steuerer, J.; Stoll, K.; Strom, David M.; Strohmer, R.; Surrow, B.; Talbot, S.D.; Taras, P.; Tarem, S.; Teuscher, R.; Thiergen, M.; Thomas, J.; Thomson, M.A.; von Torne, E.; Torrence, E.; Towers, S.; Trigger, I.; Trocsanyi, Z.; Tsur, E.; Turcot, A.S.; Turner-Watson, M.F.; Ueda, I.; Van Kooten, Rick J.; Vannerem, P.; Verzocchi, M.; Voss, H.; Wackerle, F.; Wagner, A.; Ward, C.P.; Ward, D.R.; Watkins, P.M.; Watson, A.T.; Watson, N.K.; Wells, P.S.; Wermes, N.; White, J.S.; Wilson, G.W.; Wilson, J.A.; Wyatt, T.R.; Yamashita, S.; Yekutieli, G.; Zacek, V.; Zer-Zion, D.

    1999-01-01

    The predicted effects of final state interactions such as colour reconnection are investigated by measuring properties of hadronic decays of W bosons, recorded at a centre-of-mass energy of sqrt(s)=182.7 GeV in the OPAL detector at LEP. Dependence on the modelling of hadronic W decays is avoided by comparing W+W- -> qqqq events with the non-leptonic component of W+W- -> qqlnu events. The scaled momentum distribution, its mean value, x_p, and that of the charged particle multiplicity, n_ch, are measured and found to be consistent in the two channels. The measured differences are: Diff(x_p) = +0.7 +- 0.8 +- 0.6 and Diff(n_ch) = (-0.09 +- 0.09 +-0.05)*10**-2. In addition, measurements of rapidity and thrust are performed for W+W- -> qqqq events. The data are described well by standard QCD models and disfavour one model of colour reconnection within the ARIADNE program. The current implementation of the ELLIS-GEIGER model of colour reconnection is excluded. At the current level of statistical precision no evidenc...

  10. Effect of resin chemistry on depth of cure and cytotoxicity of dental resin composites

    International Nuclear Information System (INIS)

    Susila Anand, V.; Balasubramanian, Venkatesh

    2014-01-01

    Highlights: • Dental composites have differences in polymerization within 2 mm thickness. • Degree of conversion alone may not affect the biocompatibility of composite. • Unreacted double bonds in dental composites may influence biocompatibility. • Magnitude of double bonds depends on the polymerization and chemical composition. • These influence biocompatibility especially if they possess lipophylic properties. -- Abstract: New dental composite restorative materials are being introduced aiming to overcome the disadvantages of contemporary materials. Hence there is a need to analyze the critical properties of these composites to aid in clinical application. This study aims to comparatively analyze the degree of conversion (DC), residual reactivity (DBC/reactivity) and cytotoxicity of 2 composites based on different resin chemistry. Ceram X and Filtek P90 were used in the study to prepare disc shaped samples of 2 mm thickness and 4 mm diameter. The samples for cytotoxicity were cured for 40 s and those of Fourier Transform Infra-red Spectroscopy (FTIR) (DBC/reactivity and DC) for 5 s, 10 s, 20 s and 40 s, at an average intensity of 800 mW/cm 2 with Quartz–Tungsten–Halogen (QTH) light. DC was calculated in 60–100 μm thick and 6 mm diameter samples. Double bonds concentration/reactivity was measured in approximately 80 μm thick sections prepared from the 2 mm thick discs using a hard tissue microtome. The cell viability was scored by Trypan blue exclusion staining technique at 24 h and 48 h. Both composites showed a progressive increase in double bonds/reactivity as the distance from curing probe increased which was inversely proportional to the curing time. The DC of Filtek P90 was 20% and 96% and that of Ceram X 33% and 50% at 5 s and 40 s, respectively. Ceram X showed statistically significantly higher cell viability score at both 24 h and 48 h than Filtek P90. The results were statistically analyzed using non-parametric Kruskal–Wallis, Mann

  11. Effect of resin chemistry on depth of cure and cytotoxicity of dental resin composites

    Energy Technology Data Exchange (ETDEWEB)

    Susila Anand, V. [Rehabilitation Bioengineering Group, Department of Engineering Design, Indian Institute of Technology Madras, Chennai 600036 (India); Department of Conservative Dentistry and Endodontics, Saveetha Dental College, Saveetha University, Chennai 600077 (India); Balasubramanian, Venkatesh, E-mail: chanakya@iitm.ac.in [Rehabilitation Bioengineering Group, Department of Engineering Design, Indian Institute of Technology Madras, Chennai 600036 (India)

    2014-02-15

    Highlights: • Dental composites have differences in polymerization within 2 mm thickness. • Degree of conversion alone may not affect the biocompatibility of composite. • Unreacted double bonds in dental composites may influence biocompatibility. • Magnitude of double bonds depends on the polymerization and chemical composition. • These influence biocompatibility especially if they possess lipophylic properties. -- Abstract: New dental composite restorative materials are being introduced aiming to overcome the disadvantages of contemporary materials. Hence there is a need to analyze the critical properties of these composites to aid in clinical application. This study aims to comparatively analyze the degree of conversion (DC), residual reactivity (DBC/reactivity) and cytotoxicity of 2 composites based on different resin chemistry. Ceram X and Filtek P90 were used in the study to prepare disc shaped samples of 2 mm thickness and 4 mm diameter. The samples for cytotoxicity were cured for 40 s and those of Fourier Transform Infra-red Spectroscopy (FTIR) (DBC/reactivity and DC) for 5 s, 10 s, 20 s and 40 s, at an average intensity of 800 mW/cm{sup 2} with Quartz–Tungsten–Halogen (QTH) light. DC was calculated in 60–100 μm thick and 6 mm diameter samples. Double bonds concentration/reactivity was measured in approximately 80 μm thick sections prepared from the 2 mm thick discs using a hard tissue microtome. The cell viability was scored by Trypan blue exclusion staining technique at 24 h and 48 h. Both composites showed a progressive increase in double bonds/reactivity as the distance from curing probe increased which was inversely proportional to the curing time. The DC of Filtek P90 was 20% and 96% and that of Ceram X 33% and 50% at 5 s and 40 s, respectively. Ceram X showed statistically significantly higher cell viability score at both 24 h and 48 h than Filtek P90. The results were statistically analyzed using non-parametric Kruskal

  12. Crystallization study of amorphous system Fe[sub 84-x]W[sub x]B[sub 16] (x = 3; 5)

    Energy Technology Data Exchange (ETDEWEB)

    Novakova, A.A.; Sidorova, G.V.; Kiseleva, T.Yu.; Szasz, A. (Dept. of Physics, State Univ., Moscow (Russia) Inst. of Metallurgy, Academy of Science, Moscow (Russia) Eoetvoes Univ., Budapest (Hungary))

    1992-10-01

    A complex study of the crystallization process of the amorphous system was carried out by Moessbauer spectroscopy, X-ray diffraction and DTA. Alloy samples crystallized at 600deg C contain the following phases: [alpha]-Fe, Fe[sub 3]B and solid solution (Fe, W)[sub 3]B. (orig.).

  13. Mathematical Modelling of Nitrate Removal from Water Using a Submerged Membrane Adsorption Hybrid System with Four Adsorbents

    Directory of Open Access Journals (Sweden)

    Mahatheva Kalaruban

    2018-01-01

    Full Text Available Excessive concentrations of nitrate in ground water are known to cause human health hazards. A submerged membrane adsorption hybrid system that includes a microfilter membrane and four different adsorbents (Dowex 21K XLT ion exchange resin (Dowex, Fe-coated Dowex, amine-grafted (AG corn cob and AG coconut copra operated at four different fluxes was used to continuously remove nitrate. The experimental data obtained in this study was simulated mathematically with a homogeneous surface diffusion model that incorporated membrane packing density and membrane correlation coefficient, and applied the concept of continuous flow stirred tank reactor. The model fit with experimental data was good. The surface diffusion coefficient was constant for all adsorbents and for all fluxes. The mass transfer coefficient increased with flux for all adsorbents and generally increased with the adsorption capacity of the adsorbents.

  14. Physical and chemical durability of cement impregnated epoxy resin

    International Nuclear Information System (INIS)

    Suryantoro

    1997-01-01

    Immobilization of simulation radioactive waste contains Cs and Sr with cement impregnated epoxy resin has been done. Low level liquid waste in 30% weight mixed cement homogeneously and then set in its curing time about 28 days. Waste from was impregnated with epoxy resin (Bisphenol-A-diglycidylether) and use Triethylenteramin as catalyst. the sample of cement impregnated epoxy resin 2.5 cm x 2.5 cm in diameter and length was tested by Paul Weber. The compressive strength was obtained of 4.08 kN.cm - 2. The sochxlet apparatus was run on flow rate of 300 ml/hour at 100 o C and during 24 hours. The leaching rate of Cs was round on 5.5 x 10 - 4 g.cm - 2.d - 1 and Sr was 6.1 x 10 - 4 g.cm - 2.d - 1 (author)

  15. Pre-heated dual-cured resin cements: analysis of the degree of conversion and ultimate tensile strength

    Directory of Open Access Journals (Sweden)

    Flávio Álvares França

    2011-04-01

    Full Text Available This study evaluated the degree of conversion (DC and ultimate tensile strength (UTS of dual-cured resin cements heated to 50º C prior to and during polymerization. Disc- and hourglass-shaped specimens of Rely X ARC (RX and Variolink II (VII were obtained using addition silicon molds. The products were manipulated at 25º C or 50º C and were subjected to 3 curing conditions: light-activation through a glass slide or through a pre-cured 2-mm thick resin composite disc, or they were allowed to self-cure (SC. All specimens were dark-stored dry for 15 days. For DC analysis, the resin cements were placed into the mold located on the center of a horizontal diamond on the attenuated total reflectance element in the optical bench of a Fourier Transformed Infrared spectrometer. Infrared spectra (n = 6 were collected between 1680 and 1500 cm-1, and DC was calculated by standard methods using changes in ratios of aliphatic-to-aromatic C=C absorption peaks from uncured and cured states. For UTS test, specimens (n = 10 were tested in tension in a universal testing machine (crosshead speed of 1 mm/min until failure. DC and UTS data were submitted to 2-way ANOVA, followed by Tukey's test (α= 5%. Both products showed higher DC at 50º C than at 25º C in all curing conditions. No significant difference in UTS was noted between most light-activated groups at 25º C and those at 50º C. VII SC groups showed higher UTS at 50º C than at 25º C (p < 0.05. Increased temperature led to higher DC, but its effects on resin cement UTS depended on the curing condition.

  16. 41 CFR 50-204.8 - Use of compressed air.

    Science.gov (United States)

    2010-07-01

    ... 41 Public Contracts and Property Management 1 2010-07-01 2010-07-01 true Use of compressed air. 50-204.8 Section 50-204.8 Public Contracts and Property Management Other Provisions Relating to Public... General Safety and Health Standards § 50-204.8 Use of compressed air. Compressed air shall not be used for...

  17. Resin Poliester Tak Jenuh Untuk Imobilisasi Resin Bekas Pengolahan Simulasi Limbah Radioaktif Cair

    Directory of Open Access Journals (Sweden)

    Herlan Martono

    2017-03-01

    Full Text Available Telah dilakukan penelitian tentang imobilisasi resin bekas pengolah limbah trans-uranium denganresin poliester tak jenuh untuk mengetahui kualitas blok polimer-limbah sebagai fungsi kandunganlimbah. Polimerisasi dilakukan dengan mencampurkan resin poliester tak jenuh dengan katalisdengan perbandingan katalis 1% dari jumlah resin poliester tak jenuh yang digunakan, kemudianditambahkan limbah cair transuranium simulasi. blok polimer-limbah yang terjadi diukur densitas,kuat tekan dengan alat Paul Weber, dan laju pelindihan dengan alat soxhlet pada 100 0C dan 1 atmselama 6 jam. Blok polimer dibuat dengan kandungan limbah 10, 20, 30, 40, dan 50 % berat. Hasilpenelitian menunjukkan bahwa semakin besar kandungan limbah maka kuat tekan blok polimerlimbahsemakin kecil, sedangkan laju pelindihannya semakin besar. Berdasarkan kuat tekan dan lajupelindihan, maka hasil terbaik diperoleh untuk blok-polimer dengan kandungan limbah 20 % dan 30%.

  18. Measurement of the W-boson PT distribution in bar pp collisions at √s =1.8 TeV

    International Nuclear Information System (INIS)

    Abe, F.; Amidei, D.; Apollinari, G.; Atac, M.; Auchincloss, P.; Baden, A.R.; Bamberger, A.; Barnett, B.A.; Barbaro-Galtieri, A.; Barnes, V.E.; Bedeschi, F.; Behrends, S.; Belforte, S.; Bellettini, G.; Bellinger, J.; Bensinger, J.; Beretvas, A.; Berge, J.P.; Bertolucci, S.; Bhadra, S.; Binkley, M.; Blair, R.; Blocker, C.; Bolognesi, V.; Booth, A.W.; Boswell, C.; Brandenburg, G.; Brown, D.; Buckley, E.; Budd, H.S.; Byon, A.; Byrum, K.L.; Campagnari, C.; Campbell, M.; Carey, R.; Carithers, W.; Carlsmith, D.; Carroll, J.T.; Cashmore, R.; Cervelli, F.; Chadwick, K.; Chiarelli, G.; Chinowsky, W.; Cihangir, S.; Clark, A.G.; Connor, D.; Contreras, M.; Cooper, J.; Cordelli, M.; Crane, D.; Curatolo, M.; Day, C.; Dell'Agnello, S.; Dell'Orso, M.; Demortier, L.; Derwent, P.F.; Devlin, T.; DiBitonto, D.; Drucker, R.B.; Elias, J.E.; Ely, R.; Eno, S.; Errede, S.; Esposito, B.; Flaugher, B.; Foster, G.W.; Franklin, M.; Freeman, J.; Frisch, H.; Fukui, Y.; Funayama, Y.; Garfinkel, A.F.; Gauthier, A.; Geer, S.; Giannetti, P.; Giokaris, N.; Giromini, P.; Gladney, L.; Gold, M.; Goulianos, K.; Grassmann, H.; Grosso-Pilcher, C.; Haber, C.; Hahn, S.R.; Handler, R.; Hara, K.; Harris, R.M.; Hauser, J.; Hessing, T.; Hollebeek, R.; Holloway, L.; Hu, P.; Hubbard, B.; Huffman, B.T.; Hughes, R.; Hurst, P.; Huth, J.; Incagli, M.; Ino, T.; Iso, H.; Jensen, H.; Jessop, C.P.; Johnson, R.P.; Joshi, U.; Kadel, R.W.; Kamon, T.; Kanda, S.; Kardelis, D.A.; Karliner, I.; Kearns, E.; Keeble, L.; Kephart, R.; Kesten, P.; Keup, R.M.; Keutelian, H.; Kim, S.; Kirsch, L.; Kondo, K.; Kuhlmann, S.E.; Kuns, E.; Laasanen, A.T.; Lamoureux, J.I.; Leone, S.; Li, W.; Liss, T.M.; Lockyer, N.; Luchini, C.B.; Maas, P.; Mangano, M.; Marriner, J.P.; Markeloff, R.; Markosky, L.A.; Mattingly, R.; McIntyre, P.; Menzione, A.; Meyer, T.; Mikamo, S.; Miller, M.; Mimashi, T.; Miscetti, S.; Mishina, M.; Miyashita, S.; Morita, Y.; Moulding, S.; Mukherjee, A.; Nakae, L.F.; Nakano, I.; Nelson, C.; Newman-Holmes, C.; Ng, J.S.T.

    1991-01-01

    Using the Collider Detector at Fermilab, the W-boson differential cross section dσ/dP T is measured using W→eν events in proton-antiproton collisions at √s =1.8 TeV. A next-to-leading-order theoretical calculation agrees well with the data. The cross section (σ) for P T >50 GeV/c is measured to be 423±58(stat)±108(syst) pb

  19. CW 50W/M2 = 10.9 diode laser source by spectral beam combining based on a transmission grating.

    Science.gov (United States)

    Zhang, Jun; Peng, Hangyu; Fu, Xihong; Liu, Yun; Qin, Li; Miao, Guoqing; Wang, Lijun

    2013-02-11

    An external cavity structure based on the -1st transmission grating is introduced to spectral beam combining a 970 nm diode laser bar. A CW output power of 50.8 W, an electro-optical conversion efficiency of 45%, a spectral beam combining efficiency of 90.2% and a holistic M(2) value of 10.9 are achieved. This shows a way for a diode laser source with several KW power and diffraction-limited beam quality at the same time.

  20. Bracket bond strength and cariostatic potential of an experimental resin adhesive system containing Portland cement.

    Science.gov (United States)

    Iijima, Masahiro; Hashimoto, Masanori; Nakagaki, Susumu; Muguruma, Takeshi; Kohda, Naohisa; Endo, Kazuhiko; Mizoguchi, Itaru

    2012-09-01

    To determine if a new experimental resin-based material containing Portland cement (PC) can help prevent enamel caries while providing adequate shear bond strength (SBS). Brackets were bonded to human premolars with experimental resin-based adhesive pastes composed of three weight rations of resin and PC powder (PC 30, 7:3; PC 50, 5:5; PC 70, 3:7; n  =  7). Self-etching primer (SEP) adhesive (Transbond Plus) and resin-modified glass ionomer cement (RMGIC) adhesive (Fuji Ortho FC Automix) were used for comparison. All of the bonded teeth were subjected to alternating immersion in demineralizing (pH 4.55) and remineralizing (pH 6.8) solutions for 14 days. The SBS for each sample was examined, and the Adhesive Remnant Index (ARI) score was calculated. The hardness and elastic modulus of the enamel were determined by a nanoindenter at 20 equidistant depths from the external surface at 100 µm from the bracket edge. Data were compared by one-way analysis of variance and a chi-square test. PC 50 and PC 70 showed significantly greater SBS than Fuji Ortho FC Automix, although Transbond Plus showed significantly greater SBS than other bonding systems. No significant difference in the ARI category was observed among the five groups. For specimens bonded with PC 50 and PC 70, the hardness and elastic modulus values in most locations were equivalent to those of Fuji Ortho FC Automix. Experimental resin-based bonding material containing PC provides adequate SBS and a caries-preventive effect equivalent to that of the RMGIC adhesive system.

  1. ECRH scenarios with selective heating of trapped/passing electrons in the W7-X Stellarator

    Directory of Open Access Journals (Sweden)

    Marushchenko N.B.

    2015-01-01

    Full Text Available Using specific features of the magnetic equilibrium in the W7-X stellarator, the ECRH scenarios with combined X2 and X3 modes are discussed. The RF beams for operation with X2 and X3 modes need to be launched from low- and, via the remote steering launcher, high-field-side, respectivaly, in the different crosssections of the device where the maximum and minimum of the magnetic field located. The aim is to explore the possibility of selective heating of the different classes of electrons, passing and trapped, by changing direction of the beam for X3 or switching between the beams for X2 and X3 launched from the different ports. The numerical predictions for this kind of experiments in W7-X are performed by coupled transport and ray tracing codes

  2. A universal portable appliance for stellarator W7-X power supply controlling

    International Nuclear Information System (INIS)

    Xu Weihua

    2001-01-01

    In the project Wendelstein 7-X (W7-X), the popular field bus Profibus has been determined as a uniform connection between the central control system and all the subordinate systems. A universal embedded control system has been developed for W7-X power supply controlling. Siemens 80C167CR micro-controller is used as the central control unit of the system. With a user-defined printed circuit board (PCB) several control buses, i.e., Profibus, CAN, IEEE 488, RS485 and RS232 have been connected to the micro-controller. The corresponding hardware interfaces for the control buses have been designed. A graphic liquid crystal display (LCD) and a user-defined keyboard are used as user interface. The control software will be developed with a C-like language, i.e., C166 for the controller

  3. Posterior bulk-filled resin composite restorations. A 5-year randomized controlled clinical study

    DEFF Research Database (Denmark)

    van Dijken, Jan WV; Pallesen, Ulla

    2016-01-01

    mm as needed to fill the cavity 2 mm short of the occlusal cavosurface. The occlusal part was completed with the nano-hybrid resin composite (Ceram X mono+). In the other cavity, the resin composite-only (Ceram X mono+) was placed in 2 mm increments. The restorations were evaluated using slightly......, 4 SDR-CeramX mono+ and 6 CeramX mono +-only restorations. The main reasons for failure were tooth fracture (6) and secondary caries (4). The annual failure rate (AFR) for all restorations (Class I and II) was for the bulk-filled-1.1% and for the resin composite-only restorations 1.3% (p = 0...

  4. Measurement of forward tt‾, W+bb¯ and W+cc¯ production in pp collisions at s=8 TeV

    NARCIS (Netherlands)

    Aaij, R.; Adeva, B.; Adinolfi, M.; Ajaltouni, Z.; Akar, S.; Albrecht, J.; Alessio, F.; Alexander, M.; Ali, S.; Alkhazov, G.; Alvarez Cartelle, P.; Alves, A. A.; Amato, S.; Amerio, S.; Amhis, Y.; Everse, LA; Anderlini, L.; Andreassi, G.; Andreotti, M.; Andrews, J.E.; Appleby, R. B.; Archilli, F.; d'Argent, P.; Arnau Romeu, J.; Artamonov, A.; Artuso, M.; Aslanides, E.; Auriemma, G.; Baalouch, M.; Babuschkin, I.; Carvalho Akiba, K.; Coco, V.; David, P. N Y; De Bruyn, K.; Ferro-Luzzi, M.; Ketel, T.; Koopman, R. F.; van Leerdam, J.; Merk, M.; Onderwater, C. J G; Raven, G.; Schiller, M.; Serra, N.; Snoek, H.; Storaci, B.; Syropoulos, V.; van Tilburg, J.; Tolk, S.; Tsopelas, P.; Tuning, N.

    2017-01-01

    The production of tt‾, W+bb‾ and W+cc‾ is studied in the forward region of proton–proton collisions collected at a centre-of-mass energy of 8 TeV by the LHCb experiment, corresponding to an integrated luminosity of 1.98±0.02 fb−1. The W bosons are reconstructed in the decays W→ℓν, where ℓ denotes

  5. The effect of various primers on shear bond strength of zirconia ceramic and resin composite.

    Science.gov (United States)

    Sanohkan, Sasiwimol; Kukiattrakoon, Boonlert; Larpboonphol, Narongrit; Sae-Yib, Taewalit; Jampa, Thibet; Manoppan, Satawat

    2013-11-01

    To determine the in vitro shear bond strengths (SBS) of zirconia ceramic to resin composite after various primer treatments. Forty zirconia ceramic (Zeno, Wieland Dental) specimens (10 mm in diameter and 2 mm thick) were prepared, sandblasted with 50 μm alumina, and divided into four groups (n = 10). Three experimental groups were surface treated with three primers; CP (RelyX Ceramic Primer, 3M ESPE), AP (Alloy Primer, Kuraray Medical), and MP (Monobond Plus, Ivoclar Vivadent AG). One group was not treated and served as the control. All specimens were bonded to a resin composite (Filtek Supreme XT, 3M ESPE) cylinder with an adhesive system (Adper Scotchbond Multi-Purpose Plus Adhesive, 3M ESPE) and then stored in 100% humidity at 37°C for 24 h before SBS testing in a universal testing machine. Mean SBS (MPa) were analyzed with one-way analysis of variance (ANOVA) and the Tukey's Honestly Significant Difference (HSD) test (α = 0.05). Group AP yielded the highest mean and standard deviation (SD) value of SBS (16.8 ± 2.5 MPa) and Group C presented the lowest mean and SD value (15.4 ± 1.6 MPa). The SBS did not differ significantly among the groups (P = 0.079). Within the limitations of this study, the SBS values between zirconia ceramic to resin composite using various primers and untreated surface were not significantly different.

  6. Degradation of ion spent resin using the Fenton's reagent

    International Nuclear Information System (INIS)

    Araujo, Leandro Goulart de

    2013-01-01

    The most common method for spent radioactive ion exchange resin treatment is its immobilization in cement, which reduces the radionuclides release into the environment. Although this method is efficient, it increases considerably the final volume of the waste due to the low incorporation capacity. The objective of this work was to develop a degradation method of spent resins arising from the nuclear research reactor located at the Nuclear and Energy Research Institute (IPEN-CNEN/SP), using an Advanced Oxidation Process (AOP) with Fenton's reagents. This method would allow a higher incorporation in cement. Three different resins were evaluated: cationic, anionic and a mixture of both resins. The reactions were conducted varying the catalyst concentration (25, 50, 100 and 150 mM), the volume of hydrogen peroxide (320 to 460 mL), and three different temperatures, 50, 60 and 70 deg C. Degradation of about 98% was achieved using a 50 mM catalyst solution and 330 mL of hydrogen peroxide solution. The most efficient temperature was 60 deg C. (author)

  7. The effectiveness of different polymerization protocols for class II composite resin restorations.

    NARCIS (Netherlands)

    Jong, L.C.G. de; Opdam, N.J.M.; Bronkhorst, E.M.; Roeters, F.J.M.; Wolke, J.G.C.; Geitenbeek, B.

    2007-01-01

    OBJECTIVES: To investigate the effect of reduced light exposure times on Vickers hardness (VH) of class II composite resin restorations. METHODS: Class II restorations were made in vitro in three 2mm thick increments in a human molar. Two composite resins (Clearfil AP-X; Esthet-X) were polymerized

  8. Neutron powder diffraction investigation on the crystal and magnetic structure of (Ho{sub 0.50+x}Ca{sub 0.50-x})(Mn{sub 1-x}Cr{sub x})O{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Martinelli, A; Ferretti, M [SPIN-CNR, Corso Perrone 24, 16152 Genova (Italy); Castellano, C [Dipartimento di Chimica Strutturale e Stereochimica Inorganica, Universita degli Studi di Milano, Via C Venezian 21, 20133 Milano (Italy); Cimberle, M R; Masini, R [IMEM-CNR, Via Dodecaneso 33, 16146 Genova (Italy); Ritter, C, E-mail: alberto.martinelli@spin.cnr.it [Institute Laue-Langevin, 6 rue Jules Horowitz, 38042 Grenoble Cedex 9 (France)

    2011-10-19

    The crystal and magnetic structure of (Ho{sub 0.50+x}Ca{sub 0.50-x})(Mn{sub 1-x}Cr{sub x})O{sub 3} (x = 0.00, 0.01, 0.02, 0.03) has been investigated between 5 and 300 K by means of neutron powder diffraction followed by Rietveld refinement and dc magnetic measurements. During cooling an orthorhombic to monoclinic phase transition occurs on account of the charge and orbital ordering taking place in the Mn sub-lattice; at low temperature phase separation takes place and the main monoclinic phase coexists with a secondary orthorhombic phase, whose amount slightly increases with the increase of Cr content. Cr{sup 3+} is not involved in orbital ordering or superexchange interactions. The charge and magnetic ordering are decoupled: the Mn moments order according to a CE-type structure in all samples. (paper)

  9. A method for producing a hydrocarbon resin

    Energy Technology Data Exchange (ETDEWEB)

    Tsachev, A B; Andonov, K S; Igliyev, S P

    1980-11-25

    Rock coal resin (KS), for instance, with a relative density of 1,150 to 1,190 kilograms per cubic meter, which contains 8 to 10 percent naphthaline, 1.5 to 2.8 percent phenol and 6 to 15 percent substances insoluble in toluene, or its mixture with rock coal or oil fractions of resin are subjected to distillation (Ds) in a pipe furnace with two evaporators (Is) and a distillation tower with a temperature mode in the second stage of 320 to 360 degrees and 290 to 340 degrees in the pitch compartment. A hydrocarbon resin is produced with a high carbon content, especially for the production of resin and dolomite refractory materials, as well as fuel mixtures for blast furnace and open hearth industry.

  10. Method for curing alkyd resin compositions by applying ionizing radiation

    International Nuclear Information System (INIS)

    Watanabe, T.; Murata, K.; Maruyama, T.

    1975-01-01

    An alkyd resin composition is prepared by dissolving a polymerizable alkyd resin having from 10 to 50 percent of oil length into a vinyl monomer. The polymerizable alkyd resin is obtained by a half-esterification reaction of an acid anhydride having a polymerizable unsaturated group and an alkyd resin modified with conjugated unsaturated oil having at least one reactive hydroxyl group per one molecule. The alkyd resin composition thus obtained is coated on an article, and ionizing radiation is applied on the article to cure the coated film thereon. (U.S.)

  11. T/sub 4/ radioimmunoassay with ion-exchange resin separation

    Energy Technology Data Exchange (ETDEWEB)

    Michael, J D; Modha, K [Hoechst Pharmaceuticals Research Ltd., Milton Keynes (UK)

    1977-05-28

    An explanation is provided for the reports of falsely low values of serum-thyroxine (T/sub 4/) measured by radioimmunoassay (RIA), particularly in sera containing raised concentrations of thyroxine-binding globulin (TBG) (Burr, W.A., Evans, S.E., Hogan, T.C., 1977, Lancet, April 2, 757). A re-examination of the assay technique used in commercial RIA kits ('RIA-gnost T/sub 3/' and 'RIA-gnost T/sub 4/', Behring Diagnostics) showed that blocking of binding proteins by 8-anilino-1-naphthalene sulphonic acid (ANS) was incomplete in sera with raised TBG levels. Spectroscopic determination of the blocker concentration during the time the solution was in contact with the ion exchange resin showed that 98% of the ANS was removed from solution by 10 min contact with the resin, yet 60 min was required to absorb the free T/sub 4/. There was therefore ample time for unblocked TBG to recombine with free T/sub 4/ which was then misclassified as antibody-bound T/sub 4/. The assay technique used in the kits was therefore modified. The less polar TBG blocking agent, ethylmercurithiosalicylate (merthiolate), replaced ANS and it was demonstrated that accurate T/sub 3/ and T/sub 4/ measurements in high TBG sera could be made by resin-separation RIA without resorting to prior denaturation or alcohol extraction.

  12. Microhardness of dual-polymerizing resin cements and foundation composite resins for luting fiber-reinforced posts.

    Science.gov (United States)

    Yoshida, Keiichi; Meng, Xiangfeng

    2014-06-01

    The optimal luting material for fiber-reinforced posts to ensure the longevity of foundation restorations remains undetermined. The purpose of this study was to evaluate the suitability of 3 dual-polymerizing resin cements and 2 dual-polymerizing foundation composite resins for luting fiber-reinforced posts by assessing their Knoop hardness number. Five specimens of dual-polymerizing resin cements (SA Cement Automix, G-Cem LincAce, and Panavia F2.0) and 5 specimens of dual-polymerizing foundation composite resins (Clearfil DC Core Plus and Unifil Core EM) were polymerized from the top by irradiation for 40 seconds. Knoop hardness numbers were measured at depths of 0.5, 2.0, 4.0, 6.0, 8.0, and 10.0 mm at 0.5 hours and 7 days after irradiation. Data were statistically analyzed by repeated measures ANOVA, 1-way ANOVA, and the Tukey compromise post hoc test (α=.05). At both times after irradiation, the 5 resins materials showed the highest Knoop hardness numbers at the 0.5-mm depth. At 7 days after irradiation, the Knoop hardness numbers of the resin materials did not differ significantly between the 8.0-mm and 10.0-mm depths (P>.05). For all materials, the Knoop hardness numbers at 7 days after irradiation were significantly higher than those at 0.5 hours after irradiation at all depths (Presin materials were found to decrease in the following order: DC Core Plus, Unifil Core EM, Panavia F2.0, SA Cement Automix, and G-Cem LincAce (Pcomposite resins were higher than those of the 3 dual-polymerizing resin cements, notable differences were seen among the 5 materials at all depths and at both times after irradiation. Copyright © 2014 Editorial Council for the Journal of Prosthetic Dentistry. Published by Elsevier Inc. All rights reserved.

  13. PHASE EVOLUTION AND MICROWAVE DIELECTRIC PROPERTIES OF (Li0.5Bi0.5)(W1-xMox)O4(0.0 ≤ x ≤ 1.0) CERAMICS WITH ULTRA-LOW SINTERING TEMPERATURES

    Science.gov (United States)

    Zhou, Di; Guo, Jing; Yao, Xi; Pang, Li-Xia; Qi, Ze-Ming; Shao, Tao

    2012-11-01

    The (Li0.5Bi0.5)(W1-xMox)O4(0.0 ≤ x ≤ 1.0) ceramics were prepared via the solid state reaction method. The sintering temperature decreased almost linearly from 755°C for (Li0.5Bi0.5)WO4 to 560°C for (Li0.5Bi0.5)MoO4. When the x≤0.3, a wolframite solid solution can be formed. For x = 0.4 and x = 0.6 compositions, both the wolframite and scheelite phases can be formed from the X-ray diffraction analysis, while two different kinds of grains can be revealed from the scanning electron microscopy and energy-dispersive X-ray spectrometer results. High performance of microwave dielectric properties were obtained in the (Li0.5Bi0.5)(W0.6Mo0.4)O4 ceramic sintered at 620°C with a relative permittivity of 31.5, a Qf value of 8500 GHz (at 8.2 GHz), and a temperature coefficient value of +20 ppm/°C. Complex dielectric spectra of pure (Li0.5Bi0.5)WO4 ceramic gained from the infrared spectra were extrapolated down to microwave range, and they were in good agreement with the measured values. The (Li0.5Bi0.5)(W1-xMox)O4(0.0 ≤ x ≤ 1.0) ceramics might be promising for low temperature co-fired ceramic technology.

  14. Studsvik SUPER-RAMP-II: 9x9 Project

    International Nuclear Information System (INIS)

    Djurle, S.

    1991-12-01

    EPRI participated in an international program involving ramp-testing of 9 x 9 fuel rod segments in a test reactor in Sweden. The principal objective was to establish the pellet-cladding interaction (PCI) failure threshold for this type of fuel. Several segmented fuel rods were irradiated in Dresden-2 BWR with time-averaged linear heat ratings ranging from 13 to 17 kW/m up to average burnup ranging from 26 to 34 MWd/kgU. The segments were subsequently subjected to ramp-testing in the R2 reactor at Studsvik Nuclear. The ramp-testing consisted of an initial irradiation of peak linear heat rating between 12 to 16 kW/m for about two hours, followed by a rapid increase to a power level in the range of 36 to 50 kW/m. The upper power level was maintained for twelve hours or until the fuel failure was detected. The study concluded that for 9 x 9 fuel type the PCI failure threshold is ∼38 kW/m, independent of the burnup in the range of 26 to 34 MWd/kgU. This failure threshold is about 5 kW/m greater than that of traditional 8 x 8 design. Although the significance of this difference can be argued, the interim and final fuel examinations performed in this project by destructive and nondestructive methods revealed valuable detailed information on fuel performance, which is also documented and discussed in this report

  15. Superconductors for W VII-X coils

    International Nuclear Information System (INIS)

    Maurer, W.

    1987-01-01

    Superconductor concepts are discussed with respect to operational current, cooling and bending behavior, and ac losses. The encouraging results for NbTi superconducting technology are recalled. It is argued that the WVII-X stellarator modular superconducting coils can be built just as the modular Cu coils for WVII-AS. Special attention must be paid to the dB/dt allowed for the conductor. Shape and price depend on the means used to avoid ac losses. Formula to elucidate the main physical parameters influencing ac loss behavior of superconductors are given. Configurations investigated with respect to plasma behavior are compared. Masses to be cooled were estimated for two configurations. The estimated cooling power is of the order of 3kW

  16. Continuity and enhancement of quality management during commissioning of W7-X

    Energy Technology Data Exchange (ETDEWEB)

    Vilbrandt, Reinhard, E-mail: reinhard.vilbrandt@ipp.mpg.de; Bosch, Hans-Stephan; Feist, Jost-Henrich; Klinger, Thomas

    2015-10-15

    Highlights: • Commissioning follows the W7-X structure into appropriate components, subsystems and systems. • Local and integrated commissioning steps are carried out alternately. • An exact and detailed preparation of all commissioning is absolutely necessary. • Templates support instruction manuals, safety analyses, and commissioning instructions. • Because of safety special attention must be paid to the first putting into service. - Abstract: The commissioning of Wendelstein 7-X, the first numerically optimized stellarator, is a new phase in the project. The general planning and execution of the commissioning of the entire W7-X system follow its structure into appropriate components, subsystems and systems. The approach for taking these systems into operation will lead to so-called local commissioning which is usually executed for individual systems in connection with the necessary peripheral devices and auxiliary systems. The subsequent step-wise testing and commissioning of the systems in connection with the central device of W7-X, including the central safety control, and the central data acquisition system is performed in the second step, the so-called integrated commissioning. This leads directly to the preparation of first plasma operation. New organizational and quality management elements have been added to the running system, or existing, proven tools have been modified. The major new organizational structures and tasks and the quality planning and assurance tools are described in more detail. The experience during the first commissioning steps of the vacuum and cryogenic systems is outlined.

  17. Characterization of monolith block of spent resin cementation

    International Nuclear Information System (INIS)

    Prayitno; Endro-Kismolo; Isman MT

    1996-01-01

    Spent resin immobilization process with cement was done to prevent release of radionuclide in the ultimate storage or disposal. The varied Composition of water/cement ratio in the cementation process were 0.3; 0.4; 0.5 and the various weight of resin waste are 25 g, 37.5 g and 50 gram. The compressive strength of the various water/cement ratio without spent resin was bigger than 0.3. This investigation proved that the compressive strength of Tiga Roda cement was bigger than those of Gresik cement or Nusantara cement. The compressive of the cement block of were the spent resin cementation was influenced by the water/cement ratio and the total spent resin addition. The best condition reached at the water/cement ratio of 0.3 and 25 gram spent resin, was compressive strength of 17.86 N/mm 2 . Leaching rate of the various weight composition of spent resin cementation for 91 days were between 10 -2 - 10 -4 gram.cm -2 .day -1

  18. Initial polishing time affects gloss retention in resin composites.

    Science.gov (United States)

    Waheeb, Nehal; Silikas, Nick; Watts, David

    2012-10-01

    To determine the effect of finishing and polishing time on the surface gloss of various resin-composites before and after simulated toothbrushing. Eight representative resin-composites (Ceram X mono, Ceram X duo, Tetric EvoCeram, Venus Diamond, EsteliteSigma Quick, Esthet.X HD, Filtek Supreme XT and Spectrum TPH) were used to prepare 80 disc-shaped (12 mm x 2 mm) specimens. The two step system Venus Supra was used for polishing the specimens for 3 minutes (Group A) and 10 minutes (Group B). All specimens were subjected to 16,000 cycles of simulated toothbrushing. The surface gloss was measured after polishing and after brushing using the gloss meter. Results were evaluated using one way ANOVA, two ways ANOVA and Dennett's post hoc test (P = 0.05). Group B (10-minute polishing) resulted in higher gloss values (GV) for all specimens compared to Group A (3 minutes). Also Group B showed better gloss retention compared to Group A after simulated toothbrushing. In each group, there was a significant difference between the polished composite resins (P gloss after the simulated toothbrushing.

  19. Spray drying of bead resins: feasibility tests

    International Nuclear Information System (INIS)

    Gay, R.L.; Grantham, L.F.; Jones, L.J.

    1984-01-01

    Rockwell International has developed a volume reduction system for low-level reactor wastes based on drying the wastes in a heated-air spray dryer. The drying of slurries of sodium sulfate, boric acid, and powdered ion exchange resins was demonstrated in previous tests. The drying of bead ion exchange resins can be especially difficult due to the relatively large size of bead resins (about 500 to 800 microns) and their natural affinity for water. This water becomes part of the pore structure of the resins and normally comprises 50 t 60 wt % of the resin weight. A 76-cm-diameter spray dryer was used for feasibility tests of spray drying of cation and anion bead resins. These resins were fed to the dryer in the as-received form (similar to dewatered resins) and as slurries. A dry, free-flowing product was produced in all the tests. The volume of the spray-dried product was one-half to one-third the volume of the as-received material. An economic analysis was made of the potential cost savings that can be achieved using the Rockwel spray dryer system. In-plant costs, transportation costs, and burial costs of spray-dried resins were compared to similar costs for disposal of dewatered resins. A typical utility producing 170 m 3 (6,000 ft 3 ) per year of dewatered resins can save $600,000 to $700,000 per year using this volume reduction system

  20. Removal of Pb2+ from aqueous solutions by a high-efficiency resin

    International Nuclear Information System (INIS)

    Guo, Hao; Ren, Yongzheng; Sun, Xueliang; Xu, Yadi; Li, Xuemei; Zhang, Tiancheng; Kang, Jianxiong; Liu, Dongqi

    2013-01-01

    The removal of Pb 2+ from aqueous solution by 732 cation-exchange resin in sodium type (732-CR) has been studied in batch experiments at varying pH (2.0–8.0), Pb 2+ concentration (50–200 mg/L), contact time (5–300 min), temperature (288–308 K) and resin dose (0.125–0.75 g/L). The experimental data show that the ion-exchange process was dependent on pH and temperature, the optimal exchange capacity was found at pH 4.0, and higher temperature was beneficial to lead sorption. Kinetic data indicate that the ion-exchange process followed a pseudo-first order model. The equilibrium exchange capacity could be reached at approximately 4 h, and the maximum sorption capacity of Pb 2+ at pH 4.0 was 396.8 mg/g resin. The equilibrium data were evaluated with Langmuir and Freundlich model, and were best fitted with Langmuir model. The thermodynamic parameters for removal of Pb 2+ indicate that the reaction was spontaneous and endothermic. Additionally, column tests were conducted by using both synthetic solution and effluents from lead battery industry. The regeneration of resin was performed for two sorption-regeneration cycles by 1 M NaOH, and the results show that effective regeneration was achieved by this method.

  1. Electrochemical behavior of NixW1−x materials as catalyst for hydrogen evolution reaction in alkaline media

    International Nuclear Information System (INIS)

    Oliver-Tolentino, Miguel A.; Arce-Estrada, Elsa M.; Cortés-Escobedo, Claudia A.; Bolarín-Miro, Ana M.; Sánchez-De Jesús, Félix; González-Huerta, Rosa de G.; Manzo-Robledo, Arturo

    2012-01-01

    Highlights: ► The electrochemical techniques used in this study elucidated the Ni–W surface state. ► The Ni–W materials were effective for the hydrogen evolution reaction. ► The prepared alloys exhibited higher catalytic activity than their precursors. ► The preparation method is relatively simple and effective procedure. - Abstract: In the present work, results of electrochemical evaluation, as well as morphological and structural characterization of Ni x W 1−x materials with x = 0.77, 0.64, 0.4, 0.19 and 0.07 processed by means of high energy ball milling from high purity powders are presented. Also, the electrocatalytic performance on the hydrogen evolution reaction (HER) of the Ni x W 1−x materials evaluated by linear polarization and cyclic voltammetry techniques in alkaline media at room temperature is discussed. The structural and morphological characterization of the as-prepared materials was carried out using X-ray diffraction (XRD) and scanning electron microscopy (SEM). Results indicated a small-particle clusters and solid solution formation. According to the kinetics parameters the best electrocatalytic activity was observed at Ni 64 W 36 .

  2. User Control Interface for W7-X Plasma Operation

    International Nuclear Information System (INIS)

    Spring, A.; Laqua, H.; Schacht, J.

    2006-01-01

    The WENDELSTEIN 7-X fusion experiment will be a highly complex device operated by a likewise complex control system. The fundamental configuration of the W7-X control system follows two major design principles: It reflects the strict hierarchy of the machine set-up with a set of subordinated components, which in turn can be run autonomously during commissioning and testing. Secondly, it links the basic machine operation (mainly given by the infrastructure status and the components readiness) and the physics program execution (i.e. plasma operation) on each hierarchy level and on different time scales. The complexity of the control system implies great demands on appropriate user interfaces: specialized tools for specific control tasks allowing a dedicated view on the subject to be controlled, hiding complexity wherever possible and reasonable, providing similar operation methods on each hierarchy level and both manual interaction possibilities and a high degree of intelligent automation. The contribution will describe the operation interface for experiment control including the necessary links to the machine operation. The users of ' Xcontrol ' will be both the W7-X session leaders during plasma discharge experiments and the components' or diagnostics' operators during autonomous mode or even laboratory experiments. The main ' Xcontrol ' features, such as program composition and validation, manual and automatic control instruments, resource survey, and process monitoring, will be presented. The implementation principles and the underlying communication will be discussed. (author)

  3. Determination of calcium and magnesium in nuclear grade alumina by ion chromatography technique

    International Nuclear Information System (INIS)

    Hespanhol, E.C.B.; Pires, M.A.F.; Atalla, L.T.

    1987-07-01

    A simple method for solubilization of alumina and separation of magnesium and calcium from alumina matrix was developed by initial coprecipitation of those elements with iron(III) hydroxide. Calcium and magnesium were later separated from iron chloride anionic complex in a Dowex 1-X 10 anionic exchange resin. The ion chromatography tecnnique was employed for the analysis of calcium and magnesium. One hundred percent recovery for calcium and magnesium was obtained in their separation from alumina. A precision of 6% and 10% for magnesium and calcium, respectively, was obtained in alumina samples analysis which contain less than 0,02% of magnesium and less than 0,08% of calcium. (Author) [pt

  4. Formation of carbon nanosheets via simultaneous activation and catalytic carbonization of macroporous anion-exchange resin for supercapacitors application.

    Science.gov (United States)

    Peng, Hui; Ma, Guofu; Sun, Kanjun; Mu, Jingjing; Zhang, Zhe; Lei, Ziqiang

    2014-12-10

    Two-dimensional mesoporous carbon nanosheets (CNSs) have been prepared via simultaneous activation and catalytic carbonization route using macroporous anion-exchange resin (AER) as carbon precursor and ZnCl2 and FeCl3 as activating agent and catalyst, respectively. The iron catalyst in the skeleton of the AER may lead to carburization to form a sheetlike structure during the carbonization process. The obtained CNSs have a large number of mesopores, a maximum specific surface area of 1764.9 m(2) g(-1), and large pore volume of 1.38 cm(3) g(-1). As an electrode material for supercapacitors application, the CNSs electrode possesses a large specific capacitance of 283 F g(-1) at 0.5 A g(-1) and excellent rate capability (64% retention ratio even at 50 A g(-1)) in 6 mol L(-1) KOH. Furthermore, CNSs symmetric supercapacitor exhibits specific energies of 17.2 W h kg(-1) at a power density of 224 W kg(-1) operated in the voltage range of 0-1.8 V in 0.5 mol L(-1) Na2SO4 aqueous electrolyte, and outstanding cyclability (retains about 96% initial capacitance after 5000 cycles).

  5. W-Band Transmission MeasurementS and X-Band Dielectric Properties Measurements for a Radome Material Sample

    Science.gov (United States)

    Cravey, Robin L.; Tiemsin, Pacita I.

    1997-01-01

    This paper describes measurements which were performed on a sample of radome material in the Electromagnetic Properties Measurements Laboratory (EPML). The purpose of the measurements described in this paper was to determine the one-way transmission loss through the flat panel of radome material for a frequency range of 84 to 94 GHz, for varying incidence angles. The panel, which was manufactured by Norton Performance Plastics Corporation, was provided to the EPML by TRW. The size of the panel is 40 in x 36 in x 0.422 in and consists of a foam material with one side coated with a smooth white coating (this side will be referred to as the front side). The dielectric properties of the foam material from the inside of the panel were also determined at X-band (8.2-12.4 GHz). The W-band free space measurements are presented first, followed by the X-band dielectric properties measurements.

  6. Progress of the 10 MW ECRH System for W7-X

    International Nuclear Information System (INIS)

    Michel, G.; Brand, P.; Dammertz, G.

    2003-01-01

    The electron cyclotron resonance heating system for the W7-X stellarator is a joint effort of the Max-Planck-Institut fuer Plasmaphysik in Greifswald, the Institut fuer Plasmaforschung Stuttgart and the Forschungszentrum Karlsruhe under the supervision of the latter. Currently it is being constructed at the Greifswald branch of IPP. It will consist of 10 gyrotrons (each with 1 MW 140 GHz in the CW regime) and a quasi optical multi-beam transmission line. W7-X gyrotron candidates are being developed separately in Western Europe and the USA. The prototype phase of the gyrotrons is almost over and significant results have been achieved. The manufacturing of the transmission line is ongoing. An overview over the system including data acquisition and control issues will be given and the current status of the construction will be presented. (authors)

  7. Structural features of resorcinol–formaldehyde resin chars and interfacial behavior of water co-adsorbed with low-molecular weight organics

    International Nuclear Information System (INIS)

    Gun’ko, Vladimir M.; Bogatyrov, Viktor M.; Turov, Vladimir V.; Leboda, Roman; Skubiszewska-Zięba, Jadwiga; Urubkov, Iliya V.

    2013-01-01

    Products of resorcinol–formaldehyde resin carbonization (chars) are characterized by different morphology (particle shape and sizes) and texture (specific surface area, pore volume and pore size distribution) depending on water content during resin polymerization. At a low amount of water (C w = 37.8 wt.%) during synthesis resulting in strongly cross-linked polymers, carbonization gives nonporous particles. An increase in the water content to 62.7 wt.% results in a nano/mesoporous char, but if C w = 73.3 wt.%, a char is purely nanoporous. Despite these textural differences, the Raman spectra of all the chars are similar because of the similarity in the structure of their carbon sheets with a significant contribution of sp 3 C atoms. However, the difference in the spatial organization of the carbon sheet stacks in the particles results in the significant differences in the textural and morphological characteristics and in the adsorption properties of chars with respect to water, methane, benzene, hydrogen, methylene chloride, and dimethylsulfoxide.

  8. Structural features of resorcinol–formaldehyde resin chars and interfacial behavior of water co-adsorbed with low-molecular weight organics

    Energy Technology Data Exchange (ETDEWEB)

    Gun’ko, Vladimir M., E-mail: vlad_gunko@ukr.net [Chuiko Institute of Surface Chemistry, 17 General Naumov Street, 03164 Kyiv (Ukraine); Bogatyrov, Viktor M.; Turov, Vladimir V. [Chuiko Institute of Surface Chemistry, 17 General Naumov Street, 03164 Kyiv (Ukraine); Leboda, Roman; Skubiszewska-Zięba, Jadwiga [Faculty of Chemistry, Maria Curie-Skłodowska University, 20031 Lublin (Poland); Urubkov, Iliya V. [Kurdyumov Institute of Metal Physics, 36 Vernadsky Boulevard, 03142 Kyiv (Ukraine)

    2013-10-15

    Products of resorcinol–formaldehyde resin carbonization (chars) are characterized by different morphology (particle shape and sizes) and texture (specific surface area, pore volume and pore size distribution) depending on water content during resin polymerization. At a low amount of water (C{sub w} = 37.8 wt.%) during synthesis resulting in strongly cross-linked polymers, carbonization gives nonporous particles. An increase in the water content to 62.7 wt.% results in a nano/mesoporous char, but if C{sub w} = 73.3 wt.%, a char is purely nanoporous. Despite these textural differences, the Raman spectra of all the chars are similar because of the similarity in the structure of their carbon sheets with a significant contribution of sp{sup 3} C atoms. However, the difference in the spatial organization of the carbon sheet stacks in the particles results in the significant differences in the textural and morphological characteristics and in the adsorption properties of chars with respect to water, methane, benzene, hydrogen, methylene chloride, and dimethylsulfoxide.

  9. Measurement of the $W^+W^-$ cross section in pp collisions at $\\sqrt{s} =$ 8 TeV and limits on anomalous gauge couplings

    CERN Document Server

    Khachatryan, Vardan; Tumasyan, Armen; Adam, Wolfgang; Aşılar, Ece; Bergauer, Thomas; Brandstetter, Johannes; Brondolin, Erica; Dragicevic, Marko; Erö, Janos; Flechl, Martin; Friedl, Markus; Fruehwirth, Rudolf; Ghete, Vasile Mihai; Hartl, Christian; Hörmann, Natascha; Hrubec, Josef; Jeitler, Manfred; Knünz, Valentin; König, Axel; Krammer, Manfred; Krätschmer, Ilse; Liko, Dietrich; Matsushita, Takashi; Mikulec, Ivan; Rabady, Dinyar; Rahbaran, Babak; Rohringer, Herbert; Schieck, Jochen; Schöfbeck, Robert; Strauss, Josef; Treberer-Treberspurg, Wolfgang; Waltenberger, Wolfgang; Wulz, Claudia-Elisabeth; Mossolov, Vladimir; Shumeiko, Nikolai; Suarez Gonzalez, Juan; Alderweireldt, Sara; Cornelis, Tom; De Wolf, Eddi A; Janssen, Xavier; Knutsson, Albert; Lauwers, Jasper; Luyckx, Sten; Ochesanu, Silvia; Rougny, Romain; Van De Klundert, Merijn; Van Haevermaet, Hans; Van Mechelen, Pierre; Van Remortel, Nick; Van Spilbeeck, Alex; Abu Zeid, Shimaa; Blekman, Freya; D'Hondt, Jorgen; Daci, Nadir; De Bruyn, Isabelle; Deroover, Kevin; Heracleous, Natalie; Keaveney, James; Lowette, Steven; Moreels, Lieselotte; Olbrechts, Annik; Python, Quentin; Strom, Derek; Tavernier, Stefaan; Van Doninck, Walter; Van Mulders, Petra; Van Onsem, Gerrit Patrick; Van Parijs, Isis; Barria, Patrizia; Caillol, Cécile; Clerbaux, Barbara; De Lentdecker, Gilles; Delannoy, Hugo; Fasanella, Giuseppe; Favart, Laurent; Gay, Arnaud; Grebenyuk, Anastasia; Lenzi, Thomas; Léonard, Alexandre; Maerschalk, Thierry; Marinov, Andrey; Perniè, Luca; Randle-conde, Aidan; Reis, Thomas; Seva, Tomislav; Vander Velde, Catherine; Vanlaer, Pascal; Yonamine, Ryo; Zenoni, Florian; Zhang, Fengwangdong; Beernaert, Kelly; Benucci, Leonardo; Cimmino, Anna; Crucy, Shannon; Dobur, Didar; Fagot, Alexis; Garcia, Guillaume; Gul, Muhammad; Mccartin, Joseph; Ocampo Rios, Alberto Andres; Poyraz, Deniz; Ryckbosch, Dirk; Salva Diblen, Sinem; Sigamani, Michael; Strobbe, Nadja; Tytgat, Michael; Van Driessche, Ward; Yazgan, Efe; Zaganidis, Nicolas; Basegmez, Suzan; Beluffi, Camille; Bondu, Olivier; Brochet, Sébastien; Bruno, Giacomo; Castello, Roberto; Caudron, Adrien; Ceard, Ludivine; Da Silveira, Gustavo Gil; Delaere, Christophe; Favart, Denis; Forthomme, Laurent; Giammanco, Andrea; Hollar, Jonathan; Jafari, Abideh; Jez, Pavel; Komm, Matthias; Lemaitre, Vincent; Mertens, Alexandre; Nuttens, Claude; Perrini, Lucia; Pin, Arnaud; Piotrzkowski, Krzysztof; Popov, Andrey; Quertenmont, Loic; Selvaggi, Michele; Vidal Marono, Miguel; Beliy, Nikita; Hammad, Gregory Habib; Aldá Júnior, Walter Luiz; Alves, Gilvan; Brito, Lucas; Correa Martins Junior, Marcos; Hensel, Carsten; Mora Herrera, Clemencia; Moraes, Arthur; Pol, Maria Elena; Rebello Teles, Patricia; Belchior Batista Das Chagas, Ewerton; Carvalho, Wagner; Chinellato, Jose; Custódio, Analu; Melo Da Costa, Eliza; De Jesus Damiao, Dilson; De Oliveira Martins, Carley; Fonseca De Souza, Sandro; Huertas Guativa, Lina Milena; Malbouisson, Helena; Matos Figueiredo, Diego; Mundim, Luiz; Nogima, Helio; Prado Da Silva, Wanda Lucia; Santoro, Alberto; Sznajder, Andre; Tonelli Manganote, Edmilson José; Vilela Pereira, Antonio; Ahuja, Sudha; Bernardes, Cesar Augusto; De Souza Santos, Angelo; Dogra, Sunil; Tomei, Thiago; De Moraes Gregores, Eduardo; Mercadante, Pedro G; Moon, Chang-Seong; Novaes, Sergio F; Padula, Sandra; Romero Abad, David; Ruiz Vargas, José Cupertino; Aleksandrov, Aleksandar; Genchev, Vladimir; Hadjiiska, Roumyana; Iaydjiev, Plamen; Piperov, Stefan; Rodozov, Mircho; Stoykova, Stefka; Sultanov, Georgi; Vutova, Mariana; Dimitrov, Anton; Glushkov, Ivan; Litov, Leander; Pavlov, Borislav; Petkov, Peicho; Ahmad, Muhammad; Bian, Jian-Guo; Chen, Guo-Ming; Chen, He-Sheng; Chen, Mingshui; Cheng, Tongguang; Du, Ran; Jiang, Chun-Hua; Plestina, Roko; Romeo, Francesco; Shaheen, Sarmad Masood; Tao, Junquan; Wang, Chunjie; Wang, Zheng; Zhang, Huaqiao; Asawatangtrakuldee, Chayanit; Ban, Yong; Li, Qiang; Liu, Shuai; Mao, Yajun; Qian, Si-Jin; Wang, Dayong; Xu, Zijun; Zou, Wei; Avila, Carlos; Cabrera, Andrés; Chaparro Sierra, Luisa Fernanda; Florez, Carlos; Gomez, Juan Pablo; Gomez Moreno, Bernardo; Sanabria, Juan Carlos; Godinovic, Nikola; Lelas, Damir; Polic, Dunja; Puljak, Ivica; Ribeiro Cipriano, Pedro M; Antunovic, Zeljko; Kovac, Marko; Brigljevic, Vuko; Kadija, Kreso; Luetic, Jelena; Micanovic, Sasa; Sudic, Lucija; Attikis, Alexandros; Mavromanolakis, Georgios; Mousa, Jehad; Nicolaou, Charalambos; Ptochos, Fotios; Razis, Panos A; Rykaczewski, Hans; Bodlak, Martin; Finger, Miroslav; Finger Jr, Michael; Abdelalim, Ahmed Ali; Awad, Adel; Mahrous, Ayman; Radi, Amr; Calpas, Betty; Kadastik, Mario; Murumaa, Marion; Raidal, Martti; Tiko, Andres; Veelken, Christian; Eerola, Paula; Pekkanen, Juska; Voutilainen, Mikko; Härkönen, Jaakko; Karimäki, Veikko; Kinnunen, Ritva; Lampén, Tapio; Lassila-Perini, Kati; Lehti, Sami; Lindén, Tomas; Luukka, Panja-Riina; Mäenpää, Teppo; Peltola, Timo; Tuominen, Eija; Tuominiemi, Jorma; Tuovinen, Esa; Wendland, Lauri; Talvitie, Joonas; Tuuva, Tuure; Besancon, Marc; Couderc, Fabrice; Dejardin, Marc; Denegri, Daniel; Fabbro, Bernard; Faure, Jean-Louis; Favaro, Carlotta; Ferri, Federico; Ganjour, Serguei; Givernaud, Alain; Gras, Philippe; Hamel de Monchenault, Gautier; Jarry, Patrick; Locci, Elizabeth; Machet, Martina; Malcles, Julie; Rander, John; Rosowsky, André; Titov, Maksym; Zghiche, Amina; Antropov, Iurii; Baffioni, Stephanie; Beaudette, Florian; Busson, Philippe; Cadamuro, Luca; Chapon, Emilien; Charlot, Claude; Dahms, Torsten; Davignon, Olivier; Filipovic, Nicolas; Florent, Alice; Granier de Cassagnac, Raphael; Lisniak, Stanislav; Mastrolorenzo, Luca; Miné, Philippe; Naranjo, Ivo Nicolas; Nguyen, Matthew; Ochando, Christophe; Ortona, Giacomo; Paganini, Pascal; Regnard, Simon; Salerno, Roberto; Sauvan, Jean-Baptiste; Sirois, Yves; Strebler, Thomas; Yilmaz, Yetkin; Zabi, Alexandre; Agram, Jean-Laurent; Andrea, Jeremy; Aubin, Alexandre; Bloch, Daniel; Brom, Jean-Marie; Buttignol, Michael; Chabert, Eric Christian; Chanon, Nicolas; Collard, Caroline; Conte, Eric; Coubez, Xavier; Fontaine, Jean-Charles; Gelé, Denis; Goerlach, Ulrich; Goetzmann, Christophe; Le Bihan, Anne-Catherine; Merlin, Jeremie Alexandre; Skovpen, Kirill; Van Hove, Pierre; Gadrat, Sébastien; Beauceron, Stephanie; Bernet, Colin; Boudoul, Gaelle; Bouvier, Elvire; Carrillo Montoya, Camilo Andres; Chasserat, Julien; Chierici, Roberto; Contardo, Didier; Courbon, Benoit; Depasse, Pierre; El Mamouni, Houmani; Fan, Jiawei; Fay, Jean; Gascon, Susan; Gouzevitch, Maxime; Ille, Bernard; Lagarde, Francois; Laktineh, Imad Baptiste; Lethuillier, Morgan; Mirabito, Laurent; Pequegnot, Anne-Laure; Perries, Stephane; Ruiz Alvarez, José David; Sabes, David; Sgandurra, Louis; Sordini, Viola; Vander Donckt, Muriel; Verdier, Patrice; Viret, Sébastien; Xiao, Hong; Toriashvili, Tengizi; Lomidze, David; Autermann, Christian; Beranek, Sarah; Edelhoff, Matthias; Feld, Lutz; Heister, Arno; Kiesel, Maximilian Knut; Klein, Katja; Lipinski, Martin; Ostapchuk, Andrey; Preuten, Marius; Raupach, Frank; Schael, Stefan; Schulte, Jan-Frederik; Verlage, Tobias; Weber, Hendrik; Wittmer, Bruno; Zhukov, Valery; Ata, Metin; Brodski, Michael; Dietz-Laursonn, Erik; Duchardt, Deborah; Endres, Matthias; Erdmann, Martin; Erdweg, Sören; Esch, Thomas; Fischer, Robert; Güth, Andreas; Hebbeker, Thomas; Heidemann, Carsten; Hoepfner, Kerstin; Klingebiel, Dennis; Knutzen, Simon; Kreuzer, Peter; Merschmeyer, Markus; Meyer, Arnd; Millet, Philipp; Olschewski, Mark; Padeken, Klaas; Papacz, Paul; Pook, Tobias; Radziej, Markus; Reithler, Hans; Rieger, Marcel; Scheuch, Florian; Sonnenschein, Lars; Teyssier, Daniel; Thüer, Sebastian; Cherepanov, Vladimir; Erdogan, Yusuf; Flügge, Günter; Geenen, Heiko; Geisler, Matthias; Hoehle, Felix; Kargoll, Bastian; Kress, Thomas; Kuessel, Yvonne; Künsken, Andreas; Lingemann, Joschka; Nehrkorn, Alexander; Nowack, Andreas; Nugent, Ian Michael; Pistone, Claudia; Pooth, Oliver; Stahl, Achim; Aldaya Martin, Maria; Asin, Ivan; Bartosik, Nazar; Behnke, Olaf; Behrens, Ulf; Bell, Alan James; Borras, Kerstin; Burgmeier, Armin; Cakir, Altan; Calligaris, Luigi; Campbell, Alan; Choudhury, Somnath; Costanza, Francesco; Diez Pardos, Carmen; Dolinska, Ganna; Dooling, Samantha; Dorland, Tyler; Eckerlin, Guenter; Eckstein, Doris; Eichhorn, Thomas; Flucke, Gero; Gallo, Elisabetta; Garay Garcia, Jasone; Geiser, Achim; Gizhko, Andrii; Gunnellini, Paolo; Hauk, Johannes; Hempel, Maria; Jung, Hannes; Kalogeropoulos, Alexis; Karacheban, Olena; Kasemann, Matthias; Katsas, Panagiotis; Kieseler, Jan; Kleinwort, Claus; Korol, Ievgen; Lange, Wolfgang; Leonard, Jessica; Lipka, Katerina; Lobanov, Artur; Lohmann, Wolfgang; Mankel, Rainer; Marfin, Ihar; Melzer-Pellmann, Isabell-Alissandra; Meyer, Andreas Bernhard; Mittag, Gregor; Mnich, Joachim; Mussgiller, Andreas; Naumann-Emme, Sebastian; Nayak, Aruna; Ntomari, Eleni; Perrey, Hanno; Pitzl, Daniel; Placakyte, Ringaile; Raspereza, Alexei; Roland, Benoit; Sahin, Mehmet Özgür; Saxena, Pooja; Schoerner-Sadenius, Thomas; Schröder, Matthias; Seitz, Claudia; Spannagel, Simon; Trippkewitz, Karim Damun; Wissing, Christoph; Blobel, Volker; Centis Vignali, Matteo; Draeger, Arne-Rasmus; Erfle, Joachim; Garutti, Erika; Goebel, Kristin; Gonzalez, Daniel; Görner, Martin; Haller, Johannes; Hoffmann, Malte; Höing, Rebekka Sophie; Junkes, Alexandra; Klanner, Robert; Kogler, Roman; Lapsien, Tobias; Lenz, Teresa; Marchesini, Ivan; Marconi, Daniele; Nowatschin, Dominik; Ott, Jochen; Pantaleo, Felice; Peiffer, Thomas; Perieanu, Adrian; Pietsch, Niklas; Poehlsen, Jennifer; Rathjens, Denis; Sander, Christian; Schettler, Hannes; Schleper, Peter; Schlieckau, Eike; Schmidt, Alexander; Schwandt, Joern; Seidel, Markus; Sola, Valentina; Stadie, Hartmut; Steinbrück, Georg; Tholen, Heiner; Troendle, Daniel; Usai, Emanuele; Vanelderen, Lukas; Vanhoefer, Annika; Akbiyik, Melike; Barth, Christian; Baus, Colin; Berger, Joram; Böser, Christian; Butz, Erik; Chwalek, Thorsten; Colombo, Fabio; De Boer, Wim; Descroix, Alexis; Dierlamm, Alexander; Fink, Simon; Frensch, Felix; Giffels, Manuel; Gilbert, Andrew; Hartmann, Frank; Heindl, Stefan Michael; Husemann, Ulrich; Kassel, Florian; Katkov, Igor; Kornmayer, Andreas; Lobelle Pardo, Patricia; Maier, Benedikt; Mildner, Hannes; Mozer, Matthias Ulrich; Müller, Thomas; Müller, Thomas; Plagge, Michael; Quast, Gunter; Rabbertz, Klaus; Röcker, Steffen; Roscher, Frank; Simonis, Hans-Jürgen; Stober, Fred-Markus Helmut; Ulrich, Ralf; Wagner-Kuhr, Jeannine; Wayand, Stefan; Weber, Marc; Weiler, Thomas; Wöhrmann, Clemens; Wolf, Roger; Anagnostou, Georgios; Daskalakis, Georgios; Geralis, Theodoros; Giakoumopoulou, Viktoria Athina; Kyriakis, Aristotelis; Loukas, Demetrios; Psallidas, Andreas; Topsis-Giotis, Iasonas; Agapitos, Antonis; Kesisoglou, Stilianos; Panagiotou, Apostolos; Saoulidou, Niki; Tziaferi, Eirini; Evangelou, Ioannis; Flouris, Giannis; Foudas, Costas; Kokkas, Panagiotis; Loukas, Nikitas; Manthos, Nikolaos; Papadopoulos, Ioannis; Paradas, Evangelos; Strologas, John; Bencze, Gyorgy; Hajdu, Csaba; Hazi, Andras; Hidas, Pàl; Horvath, Dezso; Sikler, Ferenc; Veszpremi, Viktor; Vesztergombi, Gyorgy; Zsigmond, Anna Julia; Beni, Noemi; Czellar, Sandor; Karancsi, János; Molnar, Jozsef; Szillasi, Zoltan; Bartók, Márton; Makovec, Alajos; Raics, Peter; Trocsanyi, Zoltan Laszlo; Ujvari, Balazs; Mal, Prolay; Mandal, Koushik; Sahoo, Niladribihari; Swain, Sanjay Kumar; Bansal, Sunil; Beri, Suman Bala; Bhatnagar, Vipin; Chawla, Ridhi; Gupta, Ruchi; Bhawandeep, Bhawandeep; Kalsi, Amandeep Kaur; Kaur, Anterpreet; Kaur, Manjit; Kumar, Ramandeep; Mehta, Ankita; Mittal, Monika; Nishu, Nishu; Singh, Jasbir; Walia, Genius; Kumar, Ashok; Kumar, Arun; Bhardwaj, Ashutosh; Choudhary, Brajesh C; Garg, Rocky Bala; Kumar, Ajay; Malhotra, Shivali; Naimuddin, Md; Ranjan, Kirti; Sharma, Ramkrishna; Sharma, Varun; Banerjee, Sunanda; Bhattacharya, Satyaki; Chatterjee, Kalyanmoy; Dey, Sourav; Dutta, Suchandra; Jain, Sandhya; Majumdar, Nayana; Modak, Atanu; Mondal, Kuntal; Mukherjee, Swagata; Mukhopadhyay, Supratik; Roy, Ashim; Roy, Debarati; Roy Chowdhury, Suvankar; Sarkar, Subir; Sharan, Manoj; Abdulsalam, Abdulla; Chudasama, Ruchi; Dutta, Dipanwita; Jha, Vishwajeet; Kumar, Vineet; Mohanty, Ajit Kumar; Pant, Lalit Mohan; Shukla, Prashant; Topkar, Anita; Aziz, Tariq; Banerjee, Sudeshna; Bhowmik, Sandeep; Chatterjee, Rajdeep Mohan; Dewanjee, Ram Krishna; Dugad, Shashikant; Ganguly, Sanmay; Ghosh, Saranya; Guchait, Monoranjan; Gurtu, Atul; Kole, Gouranga; Kumar, Sanjeev; Mahakud, Bibhuprasad; Maity, Manas; Majumder, Gobinda; Mazumdar, Kajari; Mitra, Soureek; Mohanty, Gagan Bihari; Parida, Bibhuti; Sarkar, Tanmay; Sudhakar, Katta; Sur, Nairit; Sutar, Bajrang; Wickramage, Nadeesha; Chauhan, Shubhanshu; Dube, Sourabh; Sharma, Seema; Bakhshiansohi, Hamed; Behnamian, Hadi; Etesami, Seyed Mohsen; Fahim, Ali; Goldouzian, Reza; Khakzad, Mohsen; Mohammadi Najafabadi, Mojtaba; Naseri, Mohsen; Paktinat Mehdiabadi, Saeid; Rezaei Hosseinabadi, Ferdos; Safarzadeh, Batool; Zeinali, Maryam; Felcini, Marta; Grunewald, Martin; Abbrescia, Marcello; Calabria, Cesare; Caputo, Claudio; Chhibra, Simranjit Singh; Colaleo, Anna; Creanza, Donato; Cristella, Leonardo; De Filippis, Nicola; De Palma, Mauro; Fiore, Luigi; Iaselli, Giuseppe; Maggi, Giorgio; Maggi, Marcello; Miniello, Giorgia; My, Salvatore; Nuzzo, Salvatore; Pompili, Alexis; Pugliese, Gabriella; Radogna, Raffaella; Ranieri, Antonio; Selvaggi, Giovanna; Silvestris, Lucia; Venditti, Rosamaria; Verwilligen, Piet; Abbiendi, Giovanni; Battilana, Carlo; Benvenuti, Alberto; Bonacorsi, Daniele; Braibant-Giacomelli, Sylvie; Brigliadori, Luca; Campanini, Renato; Capiluppi, Paolo; Castro, Andrea; Cavallo, Francesca Romana; Codispoti, Giuseppe; Cuffiani, Marco; Dallavalle, Gaetano-Marco; Fabbri, Fabrizio; Fanfani, Alessandra; Fasanella, Daniele; Giacomelli, Paolo; Grandi, Claudio; Guiducci, Luigi; Marcellini, Stefano; Masetti, Gianni; Montanari, Alessandro; Navarria, Francesco; Perrotta, Andrea; Rossi, Antonio; Rovelli, Tiziano; Siroli, Gian Piero; Tosi, Nicolò; Travaglini, Riccardo; Cappello, Gigi; Chiorboli, Massimiliano; Costa, Salvatore; Giordano, Ferdinando; Potenza, Renato; Tricomi, Alessia; Tuve, Cristina; Barbagli, Giuseppe; Ciulli, Vitaliano; Civinini, Carlo; D'Alessandro, Raffaello; Focardi, Ettore; Gonzi, Sandro; Gori, Valentina; Lenzi, Piergiulio; Meschini, Marco; Paoletti, Simone; Sguazzoni, Giacomo; Tropiano, Antonio; Viliani, Lorenzo; Benussi, Luigi; Bianco, Stefano; Fabbri, Franco; Piccolo, Davide; Calvelli, Valerio; Ferro, Fabrizio; Lo Vetere, Maurizio; Monge, Maria Roberta; Robutti, Enrico; Tosi, Silvano; Brianza, Luca; Dinardo, Mauro Emanuele; Fiorendi, Sara; Gennai, Simone; Gerosa, Raffaele; Ghezzi, Alessio; Govoni, Pietro; Malvezzi, Sandra; Manzoni, Riccardo Andrea; Marzocchi, Badder; Menasce, Dario; Moroni, Luigi; Paganoni, Marco; Pedrini, Daniele; Ragazzi, Stefano; Redaelli, Nicola; Tabarelli de Fatis, Tommaso; Buontempo, Salvatore; Cavallo, Nicola; Di Guida, Salvatore; Esposito, Marco; Fabozzi, Francesco; Iorio, Alberto Orso Maria; Lanza, Giuseppe; Lista, Luca; Meola, Sabino; Merola, Mario; Paolucci, Pierluigi; Sciacca, Crisostomo; Thyssen, Filip; Azzi, Patrizia; Bacchetta, Nicola; Benato, Lisa; Bisello, Dario; Boletti, Alessio; Carlin, Roberto; Carvalho Antunes De Oliveira, Alexandra; Checchia, Paolo; Dall'Osso, Martino; Dorigo, Tommaso; Dosselli, Umberto; Gasparini, Fabrizio; Gasparini, Ugo; Gozzelino, Andrea; Lacaprara, Stefano; Margoni, Martino; Meneguzzo, Anna Teresa; Pazzini, Jacopo; Pegoraro, Matteo; Pozzobon, Nicola; Ronchese, Paolo; Simonetto, Franco; Torassa, Ezio; Tosi, Mia; Vanini, Sara; Zanetti, Marco; Zotto, Pierluigi; Zucchetta, Alberto; Zumerle, Gianni; Braghieri, Alessandro; Magnani, Alice; Montagna, Paolo; Ratti, Sergio P; Re, Valerio; Riccardi, Cristina; Salvini, Paola; Vai, Ilaria; Vitulo, Paolo; Alunni Solestizi, Luisa; Biasini, Maurizio; Bilei, Gian Mario; Ciangottini, Diego; Fanò, Livio; Lariccia, Paolo; Mantovani, Giancarlo; Menichelli, Mauro; Saha, Anirban; Santocchia, Attilio; Spiezia, Aniello; Androsov, Konstantin; Azzurri, Paolo; Bagliesi, Giuseppe; Bernardini, Jacopo; Boccali, Tommaso; Broccolo, Giuseppe; Castaldi, Rino; Ciocci, Maria Agnese; Dell'Orso, Roberto; Donato, Silvio; Fedi, Giacomo; Foà, Lorenzo; Giassi, Alessandro; Grippo, Maria Teresa; Ligabue, Franco; Lomtadze, Teimuraz; Martini, Luca; Messineo, Alberto; Palla, Fabrizio; Rizzi, Andrea; Savoy-Navarro, Aurore; Serban, Alin Titus; Spagnolo, Paolo; Squillacioti, Paola; Tenchini, Roberto; Tonelli, Guido; Venturi, Andrea; Verdini, Piero Giorgio; Barone, Luciano; Cavallari, Francesca; D'imperio, Giulia; Del Re, Daniele; Diemoz, Marcella; Gelli, Simone; Jorda, Clara; Longo, Egidio; Margaroli, Fabrizio; Meridiani, Paolo; Micheli, Francesco; Organtini, Giovanni; Paramatti, Riccardo; Preiato, Federico; Rahatlou, Shahram; Rovelli, Chiara; Santanastasio, Francesco; Traczyk, Piotr; Amapane, Nicola; Arcidiacono, Roberta; Argiro, Stefano; Arneodo, Michele; Bellan, Riccardo; Biino, Cristina; Cartiglia, Nicolo; Costa, Marco; Covarelli, Roberto; Degano, Alessandro; Demaria, Natale; Finco, Linda; Kiani, Bilal; Mariotti, Chiara; Maselli, Silvia; Migliore, Ernesto; Monaco, Vincenzo; Monteil, Ennio; Musich, Marco; Obertino, Maria Margherita; Pacher, Luca; Pastrone, Nadia; Pelliccioni, Mario; Pinna Angioni, Gian Luca; Ravera, Fabio; Romero, Alessandra; Ruspa, Marta; Sacchi, Roberto; Solano, Ada; Staiano, Amedeo; Tamponi, Umberto; Belforte, Stefano; Candelise, Vieri; Casarsa, Massimo; Cossutti, Fabio; Della Ricca, Giuseppe; Gobbo, Benigno; La Licata, Chiara; Marone, Matteo; Schizzi, Andrea; Umer, Tomo; Zanetti, Anna; Chang, Sunghyun; Kropivnitskaya, Anna; Nam, Soon-Kwon; Kim, Dong Hee; Kim, Gui Nyun; Kim, Min Suk; Kong, Dae Jung; Lee, Sangeun; Oh, Young Do; Sakharov, Alexandre; Son, Dong-Chul; Brochero Cifuentes, Javier Andres; Kim, Hyunsoo; Kim, Tae Jeong; Ryu, Min Sang; Song, Sanghyeon; Choi, Suyong; Go, Yeonju; Gyun, Dooyeon; Hong, Byung-Sik; Jo, Mihee; Kim, Hyunchul; Kim, Yongsun; Lee, Byounghoon; Lee, Kisoo; Lee, Kyong Sei; Lee, Songkyo; Park, Sung Keun; Roh, Youn; Yoo, Hwi Dong; Choi, Minkyoo; Kim, Hyunyong; Kim, Ji Hyun; Lee, Jason Sang Hun; Park, Inkyu; Ryu, Geonmo; Choi, Young-Il; Choi, Young Kyu; Goh, Junghwan; Kim, Donghyun; Kwon, Eunhyang; Lee, Jongseok; Yu, Intae; Juodagalvis, Andrius; Vaitkus, Juozas; Ahmed, Ijaz; Ibrahim, Zainol Abidin; Komaragiri, Jyothsna Rani; Md Ali, Mohd Adli Bin; Mohamad Idris, Faridah; Wan Abdullah, Wan Ahmad Tajuddin; Yusli, Mohd Nizam; Casimiro Linares, Edgar; Castilla-Valdez, Heriberto; De La Cruz-Burelo, Eduard; Heredia-De La Cruz, Ivan; Hernandez-Almada, Alberto; Lopez-Fernandez, Ricardo; Sánchez Hernández, Alberto; Carrillo Moreno, Salvador; Vazquez Valencia, Fabiola; Carpinteyro, Severiano; Pedraza, Isabel; Salazar Ibarguen, Humberto Antonio; Morelos Pineda, Antonio; Krofcheck, David; Butler, Philip H; Reucroft, Steve; Ahmad, Ashfaq; Ahmad, Muhammad; Hassan, Qamar; Hoorani, Hafeez R; Khan, Wajid Ali; Khurshid, Taimoor; Shoaib, Muhammad; Bialkowska, Helena; Bluj, Michal; Boimska, Bożena; Frueboes, Tomasz; Górski, Maciej; Kazana, Malgorzata; Nawrocki, Krzysztof; Romanowska-Rybinska, Katarzyna; Szleper, Michal; Zalewski, Piotr; Brona, Grzegorz; Bunkowski, Karol; Doroba, Krzysztof; Kalinowski, Artur; Konecki, Marcin; Krolikowski, Jan; Misiura, Maciej; Olszewski, Michal; Walczak, Marek; Bargassa, Pedrame; Beirão Da Cruz E Silva, Cristóvão; Di Francesco, Agostino; Faccioli, Pietro; Ferreira Parracho, Pedro Guilherme; Gallinaro, Michele; Leonardo, Nuno; Lloret Iglesias, Lara; Nguyen, Federico; Rodrigues Antunes, Joao; Seixas, Joao; Toldaiev, Oleksii; Vadruccio, Daniele; Varela, Joao; Vischia, Pietro; Afanasiev, Serguei; Bunin, Pavel; Gavrilenko, Mikhail; Golutvin, Igor; Gorbunov, Ilya; Kamenev, Alexey; Karjavin, Vladimir; Konoplyanikov, Viktor; Lanev, Alexander; Malakhov, Alexander; Matveev, Viktor; Moisenz, Petr; Palichik, Vladimir; Perelygin, Victor; Shmatov, Sergey; Shulha, Siarhei; Skatchkov, Nikolai; Smirnov, Vitaly; Zarubin, Anatoli; Golovtsov, Victor; Ivanov, Yury; Kim, Victor; Kuznetsova, Ekaterina; Levchenko, Petr; Murzin, Victor; Oreshkin, Vadim; Smirnov, Igor; Sulimov, Valentin; Uvarov, Lev; Vavilov, Sergey; Vorobyev, Alexey; Andreev, Yuri; Dermenev, Alexander; Gninenko, Sergei; Golubev, Nikolai; Karneyeu, Anton; Kirsanov, Mikhail; Krasnikov, Nikolai; Pashenkov, Anatoli; Tlisov, Danila; Toropin, Alexander; Epshteyn, Vladimir; Gavrilov, Vladimir; Lychkovskaya, Natalia; Popov, Vladimir; Pozdnyakov, Ivan; Safronov, Grigory; Spiridonov, Alexander; Vlasov, Evgueni; Zhokin, Alexander; Bylinkin, Alexander; Andreev, Vladimir; Azarkin, Maksim; Dremin, Igor; Kirakosyan, Martin; Leonidov, Andrey; Mesyats, Gennady; Rusakov, Sergey V; Vinogradov, Alexey; Baskakov, Alexey; Belyaev, Andrey; Boos, Edouard; Dubinin, Mikhail; Dudko, Lev; Ershov, Alexander; Gribushin, Andrey; Klyukhin, Vyacheslav; Kodolova, Olga; Lokhtin, Igor; Myagkov, Igor; Obraztsov, Stepan; Petrushanko, Sergey; Savrin, Viktor; Snigirev, Alexander; Azhgirey, Igor; Bayshev, Igor; Bitioukov, Sergei; Kachanov, Vassili; Kalinin, Alexey; Konstantinov, Dmitri; Krychkine, Victor; Petrov, Vladimir; Ryutin, Roman; Sobol, Andrei; Tourtchanovitch, Leonid; Troshin, Sergey; Tyurin, Nikolay; Uzunian, Andrey; Volkov, Alexey; Adzic, Petar; Ekmedzic, Marko; Milosevic, Jovan; Rekovic, Vladimir; Alcaraz Maestre, Juan; Calvo, Enrique; Cerrada, Marcos; Chamizo Llatas, Maria; Colino, Nicanor; De La Cruz, Begona; Delgado Peris, Antonio; Domínguez Vázquez, Daniel; Escalante Del Valle, Alberto; Fernandez Bedoya, Cristina; Fernández Ramos, Juan Pablo; Flix, Jose; Fouz, Maria Cruz; Garcia-Abia, Pablo; Gonzalez Lopez, Oscar; Goy Lopez, Silvia; Hernandez, Jose M; Josa, Maria Isabel; Navarro De Martino, Eduardo; Pérez-Calero Yzquierdo, Antonio María; Puerta Pelayo, Jesus; Quintario Olmeda, Adrián; Redondo, Ignacio; Romero, Luciano; Senghi Soares, Mara; Albajar, Carmen; de Trocóniz, Jorge F; Missiroli, Marino; Moran, Dermot; Brun, Hugues; Cuevas, Javier; Fernandez Menendez, Javier; Folgueras, Santiago; Gonzalez Caballero, Isidro; Palencia Cortezon, Enrique; Vizan Garcia, Jesus Manuel; Cabrillo, Iban Jose; Calderon, Alicia; Castiñeiras De Saa, Juan Ramon; De Castro Manzano, Pablo; Duarte Campderros, Jordi; Fernandez, Marcos; Gomez, Gervasio; Graziano, Alberto; Lopez Virto, Amparo; Marco, Jesus; Marco, Rafael; Martinez Rivero, Celso; Matorras, Francisco; Munoz Sanchez, Francisca Javiela; Piedra Gomez, Jonatan; Rodrigo, Teresa; Rodríguez-Marrero, Ana Yaiza; Ruiz-Jimeno, Alberto; Scodellaro, Luca; Vila, Ivan; Vilar Cortabitarte, Rocio; Abbaneo, Duccio; Auffray, Etiennette; Auzinger, Georg; Bachtis, Michail; Baillon, Paul; Ball, Austin; Barney, David; Benaglia, Andrea; Bendavid, Joshua; Benhabib, Lamia; Benitez, Jose F; Berruti, Gaia Maria; Bloch, Philippe; Bocci, Andrea; Bonato, Alessio; Botta, Cristina; Breuker, Horst; Camporesi, Tiziano; Cerminara, Gianluca; Colafranceschi, Stefano; D'Alfonso, Mariarosaria; D'Enterria, David; Dabrowski, Anne; Daponte, Vincenzo; David Tinoco Mendes, Andre; De Gruttola, Michele; De Guio, Federico; De Roeck, Albert; De Visscher, Simon; Di Marco, Emanuele; Dobson, Marc; Dordevic, Milos; Du Pree, Tristan; Dupont, Niels; Elliott-Peisert, Anna; Franzoni, Giovanni; Funk, Wolfgang; Gigi, Dominique; Gill, Karl; Giordano, Domenico; Girone, Maria; Glege, Frank; Guida, Roberto; Gundacker, Stefan; Guthoff, Moritz; Hammer, Josef; Hansen, Magnus; Harris, Philip; Hegeman, Jeroen; Innocente, Vincenzo; Janot, Patrick; Kirschenmann, Henning; Kortelainen, Matti J; Kousouris, Konstantinos; Krajczar, Krisztian; Lecoq, Paul; Lourenco, Carlos; Lucchini, Marco Toliman; Magini, Nicolo; Malgeri, Luca; Mannelli, Marcello; Martelli, Arabella; Masetti, Lorenzo; Meijers, Frans; Mersi, Stefano; Meschi, Emilio; Moortgat, Filip; Morovic, Srecko; Mulders, Martijn; Nemallapudi, Mythra Varun; Neugebauer, Hannes; Orfanelli, Styliani; Orsini, Luciano; Pape, Luc; Perez, Emmanuelle; Petrilli, Achille; Petrucciani, Giovanni; Pfeiffer, Andreas; Piparo, Danilo; Racz, Attila; Rolandi, Gigi; Rovere, Marco; Ruan, Manqi; Sakulin, Hannes; Schäfer, Christoph; Schwick, Christoph; Sharma, Archana; Silva, Pedro; Simon, Michal; Sphicas, Paraskevas; Spiga, Daniele; Steggemann, Jan; Stieger, Benjamin; Stoye, Markus; Takahashi, Yuta; Treille, Daniel; Triossi, Andrea; Tsirou, Andromachi; Veres, Gabor Istvan; Wardle, Nicholas; Wöhri, Hermine Katharina; Zagoździńska, Agnieszka; Zeuner, Wolfram Dietrich; Bertl, Willi; Deiters, Konrad; Erdmann, Wolfram; Horisberger, Roland; Ingram, Quentin; Kaestli, Hans-Christian; Kotlinski, Danek; Langenegger, Urs; Renker, Dieter; Rohe, Tilman; Bachmair, Felix; Bäni, Lukas; Bianchini, Lorenzo; Buchmann, Marco-Andrea; Casal, Bruno; Dissertori, Günther; Dittmar, Michael; Donegà, Mauro; Dünser, Marc; Eller, Philipp; Grab, Christoph; Heidegger, Constantin; Hits, Dmitry; Hoss, Jan; Kasieczka, Gregor; Lustermann, Werner; Mangano, Boris; Marini, Andrea Carlo; Marionneau, Matthieu; Martinez Ruiz del Arbol, Pablo; Masciovecchio, Mario; Meister, Daniel; Musella, Pasquale; Nessi-Tedaldi, Francesca; Pandolfi, Francesco; Pata, Joosep; Pauss, Felicitas; Perrozzi, Luca; Peruzzi, Marco; Quittnat, Milena; Rossini, Marco; Starodumov, Andrei; Takahashi, Maiko; Tavolaro, Vittorio Raoul; Theofilatos, Konstantinos; Wallny, Rainer; Aarrestad, Thea Klaeboe; Amsler, Claude; Caminada, Lea; Canelli, Maria Florencia; Chiochia, Vincenzo; De Cosa, Annapaola; Galloni, Camilla; Hinzmann, Andreas; Hreus, Tomas; Kilminster, Benjamin; Lange, Clemens; Ngadiuba, Jennifer; Pinna, Deborah; Robmann, Peter; Ronga, Frederic Jean; Salerno, Daniel; Taroni, Silvia; Yang, Yong; Cardaci, Marco; Chen, Kuan-Hsin; Doan, Thi Hien; Ferro, Cristina; Jain, Shilpi; Khurana, Raman; Konyushikhin, Maxim; Kuo, Chia-Ming; Lin, Willis; Lu, Yun-Ju; Volpe, Roberta; Yu, Shin-Shan; Bartek, Rachel; Chang, Paoti; Chang, You-Hao; Chang, Yu-Wei; Chao, Yuan; Chen, Kai-Feng; Chen, Po-Hsun; Dietz, Charles; Fiori, Francesco; Grundler, Ulysses; Hou, George Wei-Shu; Hsiung, Yee; Liu, Yueh-Feng; Lu, Rong-Shyang; Miñano Moya, Mercedes; Petrakou, Eleni; Tsai, Jui-fa; Tzeng, Yeng-Ming; Asavapibhop, Burin; Kovitanggoon, Kittikul; Singh, Gurpreet; Srimanobhas, Norraphat; Suwonjandee, Narumon; Adiguzel, Aytul; Bakirci, Mustafa Numan; Dozen, Candan; Dumanoglu, Isa; Eskut, Eda; Girgis, Semiray; Gokbulut, Gul; Guler, Yalcin; Gurpinar, Emine; Hos, Ilknur; Kangal, Evrim Ersin; Onengut, Gulsen; Ozdemir, Kadri; Polatoz, Ayse; Sunar Cerci, Deniz; Vergili, Mehmet; Zorbilmez, Caglar; Akin, Ilina Vasileva; Bilin, Bugra; Bilmis, Selcuk; Isildak, Bora; Karapinar, Guler; Surat, Ugur Emrah; Yalvac, Metin; Zeyrek, Mehmet; Albayrak, Elif Asli; Gülmez, Erhan; Kaya, Mithat; Kaya, Ozlem; Yetkin, Taylan; Cankocak, Kerem; Sen, Sercan; Vardarlı, Fuat Ilkehan; Grynyov, Boris; Levchuk, Leonid; Sorokin, Pavel; Aggleton, Robin; Ball, Fionn; Beck, Lana; Brooke, James John; Clement, Emyr; Cussans, David; Flacher, Henning; Goldstein, Joel; Grimes, Mark; Heath, Greg P; Heath, Helen F; Jacob, Jeson; Kreczko, Lukasz; Lucas, Chris; Meng, Zhaoxia; Newbold, Dave M; Paramesvaran, Sudarshan; Poll, Anthony; Sakuma, Tai; Seif El Nasr-storey, Sarah; Senkin, Sergey; Smith, Dominic; Smith, Vincent J; Bell, Ken W; Belyaev, Alexander; Brew, Christopher; Brown, Robert M; Cockerill, David JA; Coughlan, John A; Harder, Kristian; Harper, Sam; Olaiya, Emmanuel; Petyt, David; Shepherd-Themistocleous, Claire; Thea, Alessandro; Thomas, Laurent; Tomalin, Ian R; Williams, Thomas; Womersley, William John; Worm, Steven; Baber, Mark; Bainbridge, Robert; Buchmuller, Oliver; Bundock, Aaron; Burton, Darren; Casasso, Stefano; Citron, Matthew; Colling, David; Corpe, Louie; Cripps, Nicholas; Dauncey, Paul; Davies, Gavin; De Wit, Adinda; Della Negra, Michel; Dunne, Patrick; Elwood, Adam; Ferguson, William; Fulcher, Jonathan; Futyan, David; Hall, Geoffrey; Iles, Gregory; Karapostoli, Georgia; Kenzie, Matthew; Lane, Rebecca; Lucas, Robyn; Lyons, Louis; Magnan, Anne-Marie; Malik, Sarah; Nash, Jordan; Nikitenko, Alexander; Pela, Joao; Pesaresi, Mark; Petridis, Konstantinos; Raymond, David Mark; Richards, Alexander; Rose, Andrew; Seez, Christopher; Tapper, Alexander; Uchida, Kirika; Vazquez Acosta, Monica; Virdee, Tejinder; Zenz, Seth Conrad; Cole, Joanne; Hobson, Peter R; Khan, Akram; Kyberd, Paul; Leggat, Duncan; Leslie, Dawn; Reid, Ivan; Symonds, Philip; Teodorescu, Liliana; Turner, Mark; Borzou, Ahmad; Call, Kenneth; Dittmann, Jay; Hatakeyama, Kenichi; Kasmi, Azeddine; Liu, Hongxuan; Pastika, Nathaniel; Charaf, Otman; Cooper, Seth; Henderson, Conor; Rumerio, Paolo; Avetisyan, Aram; Bose, Tulika; Fantasia, Cory; Gastler, Daniel; Lawson, Philip; Rankin, Dylan; Richardson, Clint; Rohlf, James; St John, Jason; Sulak, Lawrence; Zou, David; Alimena, Juliette; Berry, Edmund; Bhattacharya, Saptaparna; Cutts, David; Dhingra, Nitish; Ferapontov, Alexey; Garabedian, Alex; Heintz, Ulrich; Laird, Edward; Landsberg, Greg; Mao, Zaixing; Narain, Meenakshi; Sagir, Sinan; Sinthuprasith, Tutanon; Breedon, Richard; Breto, Guillermo; Calderon De La Barca Sanchez, Manuel; Chauhan, Sushil; Chertok, Maxwell; Conway, John; Conway, Rylan; Cox, Peter Timothy; Erbacher, Robin; Gardner, Michael; Ko, Winston; Lander, Richard; Mulhearn, Michael; Pellett, Dave; Pilot, Justin; Ricci-Tam, Francesca; Shalhout, Shalhout; Smith, John; Squires, Michael; Stolp, Dustin; Tripathi, Mani; Wilbur, Scott; Yohay, Rachel; Cousins, Robert; Everaerts, Pieter; Farrell, Chris; Hauser, Jay; Ignatenko, Mikhail; Saltzberg, David; Takasugi, Eric; Valuev, Vyacheslav; Weber, Matthias; Burt, Kira; Clare, Robert; Ellison, John Anthony; Gary, J William; Hanson, Gail; Heilman, Jesse; Ivova PANEVA, Mirena; Jandir, Pawandeep; Kennedy, Elizabeth; Lacroix, Florent; Long, Owen Rosser; Luthra, Arun; Malberti, Martina; Olmedo Negrete, Manuel; Shrinivas, Amithabh; Wei, Hua; Wimpenny, Stephen; Branson, James G; Cerati, Giuseppe Benedetto; Cittolin, Sergio; D'Agnolo, Raffaele Tito; Holzner, André; Kelley, Ryan; Klein, Daniel; Letts, James; Macneill, Ian; Olivito, Dominick; Padhi, Sanjay; Pieri, Marco; Sani, Matteo; Sharma, Vivek; Simon, Sean; Tadel, Matevz; Vartak, Adish; Wasserbaech, Steven; Welke, Charles; Würthwein, Frank; Yagil, Avraham; Zevi Della Porta, Giovanni; Barge, Derek; Bradmiller-Feld, John; Campagnari, Claudio; Dishaw, Adam; Dutta, Valentina; Flowers, Kristen; Franco Sevilla, Manuel; Geffert, Paul; George, Christopher; Golf, Frank; Gouskos, Loukas; Gran, Jason; Incandela, Joe; Justus, Christopher; Mccoll, Nickolas; Mullin, Sam Daniel; Richman, Jeffrey; Stuart, David; Suarez, Indara; To, Wing; West, Christopher; Yoo, Jaehyeok; Anderson, Dustin; Apresyan, Artur; Bornheim, Adolf; Bunn, Julian; Chen, Yi; Duarte, Javier; Mott, Alexander; Newman, Harvey B; Pena, Cristian; Pierini, Maurizio; Spiropulu, Maria; Vlimant, Jean-Roch; Xie, Si; Zhu, Ren-Yuan; Azzolini, Virginia; Calamba, Aristotle; Carlson, Benjamin; Ferguson, Thomas; Iiyama, Yutaro; Paulini, Manfred; Russ, James; Sun, Menglei; Vogel, Helmut; Vorobiev, Igor; Cumalat, John Perry; Ford, William T; Gaz, Alessandro; Jensen, Frank; Johnson, Andrew; Krohn, Michael; Mulholland, Troy; Nauenberg, Uriel; Smith, James; Stenson, Kevin; Wagner, Stephen Robert; Alexander, James; Chatterjee, Avishek; Chaves, Jorge; Chu, Jennifer; Dittmer, Susan; Eggert, Nicholas; Mirman, Nathan; Nicolas Kaufman, Gala; Patterson, Juliet Ritchie; Rinkevicius, Aurelijus; Ryd, Anders; Skinnari, Louise; Soffi, Livia; Sun, Werner; Tan, Shao Min; Teo, Wee Don; Thom, Julia; Thompson, Joshua; Tucker, Jordan; Weng, Yao; Wittich, Peter; Abdullin, Salavat; Albrow, Michael; Anderson, Jacob; Apollinari, Giorgio; Bauerdick, Lothar AT; Beretvas, Andrew; Berryhill, Jeffrey; Bhat, Pushpalatha C; Bolla, Gino; Burkett, Kevin; Butler, Joel Nathan; Cheung, Harry; Chlebana, Frank; Cihangir, Selcuk; Elvira, Victor Daniel; Fisk, Ian; Freeman, Jim; Gottschalk, Erik; Gray, Lindsey; Green, Dan; Grünendahl, Stefan; Gutsche, Oliver; Hanlon, Jim; Hare, Daryl; Harris, Robert M; Hirschauer, James; Hooberman, Benjamin; Hu, Zhen; Jindariani, Sergo; Johnson, Marvin; Joshi, Umesh; Jung, Andreas Werner; Klima, Boaz; Kreis, Benjamin; Kwan, Simon; Lammel, Stephan; Linacre, Jacob; Lincoln, Don; Lipton, Ron; Liu, Tiehui; Lopes De Sá, Rafael; Lykken, Joseph; Maeshima, Kaori; Marraffino, John Michael; Martinez Outschoorn, Verena Ingrid; Maruyama, Sho; Mason, David; McBride, Patricia; Merkel, Petra; Mishra, Kalanand; Mrenna, Stephen; Nahn, Steve; Newman-Holmes, Catherine; O'Dell, Vivian; Pedro, Kevin; Prokofyev, Oleg; Rakness, Gregory; Sexton-Kennedy, Elizabeth; Soha, Aron; Spalding, William J; Spiegel, Leonard; Taylor, Lucas; Tkaczyk, Slawek; Tran, Nhan Viet; Uplegger, Lorenzo; Vaandering, Eric Wayne; Vernieri, Caterina; Verzocchi, Marco; Vidal, Richard; Weber, Hannsjoerg Artur; Whitbeck, Andrew; Yang, Fan; Yin, Hang; Acosta, Darin; Avery, Paul; Bortignon, Pierluigi; Bourilkov, Dimitri; Carnes, Andrew; Carver, Matthew; Curry, David; Das, Souvik; Di Giovanni, Gian Piero; Field, Richard D; Fisher, Matthew; Furic, Ivan-Kresimir; Hugon, Justin; Konigsberg, Jacobo; Korytov, Andrey; Low, Jia Fu; Ma, Peisen; Matchev, Konstantin; Mei, Hualin; Milenovic, Predrag; Mitselmakher, Guenakh; Muniz, Lana; Rank, Douglas; Rossin, Roberto; Shchutska, Lesya; Snowball, Matthew; Sperka, David; Wang, Jian; Wang, Sean-Jiun; Yelton, John; Hewamanage, Samantha; Linn, Stephan; Markowitz, Pete; Martinez, German; Rodriguez, Jorge Luis; Ackert, Andrew; Adams, Jordon Rowe; Adams, Todd; Askew, Andrew; Bochenek, Joseph; Diamond, Brendan; Haas, Jeff; Hagopian, Sharon; Hagopian, Vasken; Johnson, Kurtis F; Khatiwada, Ajeeta; Prosper, Harrison; Veeraraghavan, Venkatesh; Weinberg, Marc; Bhopatkar, Vallary; Hohlmann, Marcus; Kalakhety, Himali; Mareskas-palcek, Darren; Roy, Titas; Yumiceva, Francisco; Adams, Mark Raymond; Apanasevich, Leonard; Berry, Douglas; Betts, Russell Richard; Bucinskaite, Inga; Cavanaugh, Richard; Evdokimov, Olga; Gauthier, Lucie; Gerber, Cecilia Elena; Hofman, David Jonathan; Kurt, Pelin; O'Brien, Christine; Sandoval Gonzalez, Irving Daniel; Silkworth, Christopher; Turner, Paul; Varelas, Nikos; Wu, Zhenbin; Zakaria, Mohammed; Bilki, Burak; Clarida, Warren; Dilsiz, Kamuran; Durgut, Süleyman; Gandrajula, Reddy Pratap; Haytmyradov, Maksat; Khristenko, Viktor; Merlo, Jean-Pierre; Mermerkaya, Hamit; Mestvirishvili, Alexi; Moeller, Anthony; Nachtman, Jane; Ogul, Hasan; Onel, Yasar; Ozok, Ferhat; Penzo, Aldo; Snyder, Christina; Tan, Ping; Tiras, Emrah; Wetzel, James; Yi, Kai; Anderson, Ian; Barnett, Bruce Arnold; Blumenfeld, Barry; Fehling, David; Feng, Lei; Gritsan, Andrei; Maksimovic, Petar; Martin, Christopher; Nash, Kevin; Osherson, Marc; Swartz, Morris; Xiao, Meng; Xin, Yongjie; Baringer, Philip; Bean, Alice; Benelli, Gabriele; Bruner, Christopher; Gray, Julia; Kenny III, Raymond Patrick; Majumder, Devdatta; Malek, Magdalena; Murray, Michael; Noonan, Daniel; Sanders, Stephen; Stringer, Robert; Wang, Quan; Wood, Jeffrey Scott; Chakaberia, Irakli; Ivanov, Andrew; Kaadze, Ketino; Khalil, Sadia; Makouski, Mikhail; Maravin, Yurii; Mohammadi, Abdollah; Saini, Lovedeep Kaur; Skhirtladze, Nikoloz; Svintradze, Irakli; Toda, Sachiko; Lange, David; Rebassoo, Finn; Wright, Douglas; Anelli, Christopher; Baden, Drew; Baron, Owen; Belloni, Alberto; Calvert, Brian; Eno, Sarah Catherine; Ferraioli, Charles; Gomez, Jaime; Hadley, Nicholas John; Jabeen, Shabnam; Kellogg, Richard G; Kolberg, Ted; Kunkle, Joshua; Lu, Ying; Mignerey, Alice; Shin, Young Ho; Skuja, Andris; Tonjes, Marguerite; Tonwar, Suresh C; Apyan, Aram; Barbieri, Richard; Baty, Austin; Bierwagen, Katharina; Brandt, Stephanie; Busza, Wit; Cali, Ivan Amos; Demiragli, Zeynep; Di Matteo, Leonardo; Gomez Ceballos, Guillelmo; Goncharov, Maxim; Gulhan, Doga; Innocenti, Gian Michele; Klute, Markus; Kovalskyi, Dmytro; Lai, Yue Shi; Lee, Yen-Jie; Levin, Andrew; Luckey, Paul David; Mcginn, Christopher; Mironov, Camelia; Niu, Xinmei; Paus, Christoph; Ralph, Duncan; Roland, Christof; Roland, Gunther; Salfeld-Nebgen, Jakob; Stephans, George; Sumorok, Konstanty; Varma, Mukund; Velicanu, Dragos; Veverka, Jan; Wang, Jing; Wang, Ta-Wei; Wyslouch, Bolek; Yang, Mingming; Zhukova, Victoria; Dahmes, Bryan; Finkel, Alexey; Gude, Alexander; Hansen, Peter; Kalafut, Sean; Kao, Shih-Chuan; Klapoetke, Kevin; Kubota, Yuichi; Lesko, Zachary; Mans, Jeremy; Nourbakhsh, Shervin; Ruckstuhl, Nicole; Rusack, Roger; Tambe, Norbert; Turkewitz, Jared; Acosta, John Gabriel; Oliveros, Sandra; Avdeeva, Ekaterina; Bloom, Kenneth; Bose, Suvadeep; Claes, Daniel R; Dominguez, Aaron; Fangmeier, Caleb; Gonzalez Suarez, Rebeca; Kamalieddin, Rami; Keller, Jason; Knowlton, Dan; Kravchenko, Ilya; Lazo-Flores, Jose; Meier, Frank; Monroy, Jose; Ratnikov, Fedor; Siado, Joaquin Emilo; Snow, Gregory R; Alyari, Maral; Dolen, James; George, Jimin; Godshalk, Andrew; Iashvili, Ia; Kaisen, Josh; Kharchilava, Avto; Kumar, Ashish; Rappoccio, Salvatore; Alverson, George; Barberis, Emanuela; Baumgartel, Darin; Chasco, Matthew; Hortiangtham, Apichart; Massironi, Andrea; Morse, David Michael; Nash, David; Orimoto, Toyoko; Teixeira De Lima, Rafael; Trocino, Daniele; Wang, Ren-Jie; Wood, Darien; Zhang, Jinzhong; Hahn, Kristan Allan; Kubik, Andrew; Mucia, Nicholas; Odell, Nathaniel; Pollack, Brian; Pozdnyakov, Andrey; Schmitt, Michael Henry; Stoynev, Stoyan; Sung, Kevin; Trovato, Marco; Velasco, Mayda; Won, Steven; Brinkerhoff, Andrew; Dev, Nabarun; Hildreth, Michael; Jessop, Colin; Karmgard, Daniel John; Kellams, Nathan; Lannon, Kevin; Lynch, Sean; Marinelli, Nancy; Meng, Fanbo; Mueller, Charles; Musienko, Yuri; Pearson, Tessa; Planer, Michael; Reinsvold, Allison; Ruchti, Randy; Smith, Geoffrey; Valls, Nil; Wayne, Mitchell; Wolf, Matthias; Woodard, Anna; Antonelli, Louis; Brinson, Jessica; Bylsma, Ben; Durkin, Lloyd Stanley; Flowers, Sean; Hart, Andrew; Hill, Christopher; Hughes, Richard; Kotov, Khristian; Ling, Ta-Yung; Liu, Bingxuan; Luo, Wuming; Puigh, Darren; Rodenburg, Marissa; Winer, Brian L; Wulsin, Howard Wells; Driga, Olga; Elmer, Peter; Hardenbrook, Joshua; Hebda, Philip; Koay, Sue Ann; Lujan, Paul; Marlow, Daniel; Medvedeva, Tatiana; Mooney, Michael; Olsen, James; Palmer, Christopher; Piroué, Pierre; Quan, Xiaohang; Saka, Halil; Stickland, David; Tully, Christopher; Werner, Jeremy Scott; Zuranski, Andrzej; Malik, Sudhir; Barnes, Virgil E; Benedetti, Daniele; Bortoletto, Daniela; Gutay, Laszlo; Jha, Manoj; Jones, Matthew; Jung, Kurt; Kress, Matthew; Miller, David Harry; Neumeister, Norbert; Primavera, Federica; Radburn-Smith, Benjamin Charles; Shi, Xin; Shipsey, Ian; Silvers, David; Sun, Jian; Svyatkovskiy, Alexey; Wang, Fuqiang; Xie, Wei; Xu, Lingshan; Zablocki, Jakub; Parashar, Neeti; Stupak, John; Adair, Antony; Akgun, Bora; Chen, Zhenyu; Ecklund, Karl Matthew; Geurts, Frank JM; Guilbaud, Maxime; Li, Wei; Michlin, Benjamin; Northup, Michael; Padley, Brian Paul; Redjimi, Radia; Roberts, Jay; Rorie, Jamal; Tu, Zhoudunming; Zabel, James; Betchart, Burton; Bodek, Arie; de Barbaro, Pawel; Demina, Regina; Eshaq, Yossof; Ferbel, Thomas; Galanti, Mario; Garcia-Bellido, Aran; Goldenzweig, Pablo; Han, Jiyeon; Harel, Amnon; Hindrichs, Otto; Khukhunaishvili, Aleko; Petrillo, Gianluca; Verzetti, Mauro; Demortier, Luc; Arora, Sanjay; Barker, Anthony; Chou, John Paul; Contreras-Campana, Christian; Contreras-Campana, Emmanuel; Duggan, Daniel; Ferencek, Dinko; Gershtein, Yuri; Gray, Richard; Halkiadakis, Eva; Hidas, Dean; Hughes, Elliot; Kaplan, Steven; Kunnawalkam Elayavalli, Raghav; Lath, Amitabh; Panwalkar, Shruti; Park, Michael; Salur, Sevil; Schnetzer, Steve; Sheffield, David; Somalwar, Sunil; Stone, Robert; Thomas, Scott; Thomassen, Peter; Walker, Matthew; Foerster, Mark; Riley, Grant; Rose, Keith; Spanier, Stefan; York, Andrew; Bouhali, Othmane; Castaneda Hernandez, Alfredo; Dalchenko, Mykhailo; De Mattia, Marco; Delgado, Andrea; Dildick, Sven; Eusebi, Ricardo; Flanagan, Will; Gilmore, Jason; Kamon, Teruki; Krutelyov, Vyacheslav; Montalvo, Roy; Mueller, Ryan; Osipenkov, Ilya; Pakhotin, Yuriy; Patel, Rishi; Perloff, Alexx; Roe, Jeffrey; Rose, Anthony; Safonov, Alexei; Tatarinov, Aysen; Ulmer, Keith; Akchurin, Nural; Cowden, Christopher; Damgov, Jordan; Dragoiu, Cosmin; Dudero, Phillip Russell; Faulkner, James; Kunori, Shuichi; Lamichhane, Kamal; Lee, Sung Won; Libeiro, Terence; Undleeb, Sonaina; Volobouev, Igor; Appelt, Eric; Delannoy, Andrés G; Greene, Senta; Gurrola, Alfredo; Janjam, Ravi; Johns, Willard; Maguire, Charles; Mao, Yaxian; Melo, Andrew; Sheldon, Paul; Snook, Benjamin; Tuo, Shengquan; Velkovska, Julia; Xu, Qiao; Arenton, Michael Wayne; Boutle, Sarah; Cox, Bradley; Francis, Brian; Goodell, Joseph; Hirosky, Robert; Ledovskoy, Alexander; Li, Hengne; Lin, Chuanzhe; Neu, Christopher; Wolfe, Evan; Wood, John; Xia, Fan; Clarke, Christopher; Harr, Robert; Karchin, Paul Edmund; Kottachchi Kankanamge Don, Chamath; Lamichhane, Pramod; Sturdy, Jared; Belknap, Donald; Carlsmith, Duncan; Cepeda, Maria; Christian, Allison; Dasu, Sridhara; Dodd, Laura; Duric, Senka; Friis, Evan; Gomber, Bhawna; Hall-Wilton, Richard; Herndon, Matthew; Hervé, Alain; Klabbers, Pamela; Lanaro, Armando; Levine, Aaron; Long, Kenneth; Loveless, Richard; Mohapatra, Ajit; Ojalvo, Isabel; Perry, Thomas; Pierro, Giuseppe Antonio; Polese, Giovanni; Ross, Ian; Ruggles, Tyler; Sarangi, Tapas; Savin, Alexander; Sharma, Archana; Smith, Nicholas; Smith, Wesley H; Taylor, Devin; Woods, Nathaniel

    2016-07-15

    A measurement of the W boson pair production cross section in proton-proton collisions at $\\sqrt{s} =$ 8 TeV is presented. The data collected with the CMS detector at the LHC correspond to an integrated luminosity of 19.4 fb$^{-1}$. The $\\mathrm{W}^{+} \\mathrm{W}^{-}$ candidates are selected from events with two charged leptons, electrons or muons, and large missing transverse energy. The measured $\\mathrm{W}^{+} \\mathrm{W}^{-}$ cross section is 60.1 $\\pm$ 0.9 (stat) $\\pm$ 3.2 (exp) $\\pm$ 3.1 (theo) $\\pm$ 1.6 (lumi) pb = 60.1 $\\pm$ 4.8 pb, consistent with the standard model prediction.The $\\mathrm{W}^{+} \\mathrm{W}^{-}$ cross sections are also measured in two different fiducial phase space regions. The normalized differential cross section is measured as a function of kinematic variables of the final-state charged leptons and compared with several perturbative QCD predictions. Limits on anomalous gauge couplings associated with dimension-six operators are also given in the framework of an effective field the...

  10. Over 8 W high peak power UV laser with a high power Q-switched Nd:YVO4 oscillator and the compact extra-cavity sum-frequency mixing

    International Nuclear Information System (INIS)

    Yan, X P; Liu, Q; Gong, M; Wang, D S; Fu, X

    2009-01-01

    A 8.2 W UV laser was reported with the compact extra-cavity sum-frequency mixing. The IR fundamental frequency source was a high power and high beam quality Q-switched Nd:YVO 4 oscillator. 38 W fundamental frequency laser at 1064 nm was obtained at the pulse repetition rate of 450 kHz with the beam quality factors of M 2 x = 1.27, M 2 y = 1.21. The type I and type II phase-matched LBO crystals were used as the extra-cavity frequency doubling and mixing crystals respectively. At 38 kHz, 8.2 W UV laser at 355 nm was achieved with the pulse duration of 8 ns corresponding to the pulse peak power as high as 27 kW, and the optical-optical conversion efficiency from IR to UV was 25.6%. The output characteristics of the IR and the harmonic generations varying with the pulse repetition rate were also investigated detailedly

  11. Effect of light-curing units, post-cured time and shade of resin cement on knoop hardness.

    Science.gov (United States)

    Reges, Rogério Vieira; Costa, Ana Rosa; Correr, Américo Bortolazzo; Piva, Evandro; Puppin-Rontani, Regina Maria; Sinhoreti, Mário Alexandre Coelho; Correr-Sobrinho, Lourenço

    2009-01-01

    The aim of this study was to evaluate the Knoop hardness after 15 min and 24 h of different shades of a dual-cured resin-based cement after indirect photoactivation (ceramic restoration) with 2 light-curing units (LCUs). The resin cement Variolink II (Ivoclar Vivadent) shade XL, A2, A3 and opaque were mixed with the catalyst paste and inserted into a black Teflon mold (5 mm diameter x 1 mm high). A transparent strip was placed over the mold and a ceramic disc (Duceram Plus, shade A3) was positioned over the resin cement. Light-activation was performed through the ceramic for 40 s using quartz-tungsten-halogen (QTH) (XL 2500; 3M ESPE) or light-emitting diode (LED) (Ultrablue Is, DMC) LCUs with power density of 615 and 610 mW/cm(2), respectively. The Koop hardness was measured using a microhardness tester HMV 2 (Shimadzu) after 15 min or 24 h. Four indentations were made in each specimen. Data were subjected to ANOVA and Tukey's test (alpha=0.05). The QTH LCU provided significantly higher (pcement showed lower Knoop hardness than the other shades for both LCUs and post-cure times.

  12. X-ray resonant magnetic reflectivity of stratified magnetic structures: Eigenwave formalism and application to a W/Fe/W trilayer

    International Nuclear Information System (INIS)

    Elzo, M.; Jal, E.; Bunau, O.; Grenier, S.; Joly, Y.; Ramos, A.Y.; Tolentino, H.C.N.; Tonnerre, J.M.; Jaouen, N.

    2012-01-01

    A formalism for the reflectivity of electromagnetic waves by magnetic materials is presented with an application. It is applied to retrieve the magnetic moment density along the depth of magnetic materials with arbitrary magnetic moment direction using matricial algebra, including roughness between layers. The reflectivity is derived following a classical description with Maxwell equations and a permittivity built from the quantum scattering amplitude. Approximations on the relative power of the Thomson scattering and the magnetic terms are trackable in order to evaluate the validity of the formalism case-by-case, from the optical light regime up to soft and hard X-rays. Eigenwaves are used throughout the whole formalism. In order to illustrate the methodology, we present an application to a W/Fe/W trilayer performed at the Fe L-edge, in the soft X-ray regime. - Highlights: → Magnetism at interfaces and in thin films is increasingly studied. → X-ray resonant magnetic reflectivity yields the in depth magnetization profile in thin films. → We present a formalism and methodology to study the data. → We illustrate the technique with an example.

  13. Study of uranium (VI) in carbonate solution by potentiometric titrations and ion-exchange; Etude des solutions d'uranium (VI) en milieu carbonate par titrages potentiometriques et echange d'ions

    Energy Technology Data Exchange (ETDEWEB)

    Billon, A [Commissariat a l' Energie Atomique, 92 - Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

    1968-04-01

    The present work is devoted to the fixation of uranium (VI) on the conventional anion-exchange resin Dowex 2 X 8 in carbonate and hydrogen-carbonate media. Both media were successfully used for the recuperation of uranium (VI) from very dilute solutions. Equilibrium constant of the exchange [UO{sub 2}(CO{sub 3}){sub 3}{sup 4+}]{sub S} + 2 [CO{sub 3}{sup 2-}]{sub R} {r_reversible} [UO{sub 2}(CO{sub 3}){sub 3}{sup 4-}]{sub R} + 2[CO{sub 3}{sup 2-}]{sub S} is determined for carbonate concentration range 0.1 M to 0.6 M from partition curves. A markedly increase in the relative fixation of uranium results with: - increasing free carbonate concentration of the solution, - decreasing uranium concentration. A study in the same conditions of the fixation of molybdenum has made it possible to separate the latter from uranium by elution, the carbonate concentration being molar. It is suggested a possibility of separation on a larger scale, based upon molybdenum displacement by uranium in hydrogen-carbonate medium. (author) [French] Le present travail precise la fixation de l'uranium (VI) sur la resine echangeuse d'anions Dowex 2 X 8, en milieu carbonate et hydrogeno-carbonate. Nous en avons deduit que ces deux milieux sont egalement favorables a la recuperation de l'uranium a partir de solutions tres diluees. La constante d'equilibre de la reaction d'echange [UO{sub 2}(CO{sub 3}){sub 3}{sup 4+}]{sub S} + 2 [CO{sub 3}{sup 2-}]{sub R} {r_reversible} [UO{sub 2}(CO{sub 3}){sub 3}{sup 4-}]{sub R} + 2[CO{sub 3}{sup 2-}]{sub S} a ete determinee pour le milieu carbonate 0.1 M a 0.6 M, a partir deb courbes de partage. La fixation relative de l'uranium augmente considerablement lorsque: - la concentration du carbonate libre (respectivement hydrogenocarbonate) diminue, - la concentration de l'uranium en solution diminue. Le comportement du molybdene a ete etudie en vue de la separation uranium-molybdene. L'ion fixe sur la resine est l'ion molybdate MoO{sub 4}{sup 2-}. La separation est

  14. Study of uranium (VI) in carbonate solution by potentiometric titrations and ion-exchange; Etude des solutions d'uranium (VI) en milieu carbonate par titrages potentiometriques et echange d'ions

    Energy Technology Data Exchange (ETDEWEB)

    Billon, A. [Commissariat a l' Energie Atomique, 92 - Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

    1968-04-01

    The present work is devoted to the fixation of uranium (VI) on the conventional anion-exchange resin Dowex 2 X 8 in carbonate and hydrogen-carbonate media. Both media were successfully used for the recuperation of uranium (VI) from very dilute solutions. Equilibrium constant of the exchange [UO{sub 2}(CO{sub 3}){sub 3}{sup 4+}]{sub S} + 2 [CO{sub 3}{sup 2-}]{sub R} {r_reversible} [UO{sub 2}(CO{sub 3}){sub 3}{sup 4-}]{sub R} + 2[CO{sub 3}{sup 2-}]{sub S} is determined for carbonate concentration range 0.1 M to 0.6 M from partition curves. A markedly increase in the relative fixation of uranium results with: - increasing free carbonate concentration of the solution, - decreasing uranium concentration. A study in the same conditions of the fixation of molybdenum has made it possible to separate the latter from uranium by elution, the carbonate concentration being molar. It is suggested a possibility of separation on a larger scale, based upon molybdenum displacement by uranium in hydrogen-carbonate medium. (author) [French] Le present travail precise la fixation de l'uranium (VI) sur la resine echangeuse d'anions Dowex 2 X 8, en milieu carbonate et hydrogeno-carbonate. Nous en avons deduit que ces deux milieux sont egalement favorables a la recuperation de l'uranium a partir de solutions tres diluees. La constante d'equilibre de la reaction d'echange [UO{sub 2}(CO{sub 3}){sub 3}{sup 4+}]{sub S} + 2 [CO{sub 3}{sup 2-}]{sub R} {r_reversible} [UO{sub 2}(CO{sub 3}){sub 3}{sup 4-}]{sub R} + 2[CO{sub 3}{sup 2-}]{sub S} a ete determinee pour le milieu carbonate 0.1 M a 0.6 M, a partir deb courbes de partage. La fixation relative de l'uranium augmente considerablement lorsque: - la concentration du carbonate libre (respectivement hydrogenocarbonate) diminue, - la concentration de l'uranium en solution diminue. Le comportement du molybdene a ete etudie en vue de la separation uranium-molybdene. L'ion fixe sur la resine est l

  15. Simulation of pulse height analysis soft X-ray spectra expected from W7-X

    Science.gov (United States)

    Jabłoński, S.; Czarnecka, A.; Kubkowska, M.; Ryć, L.; Weller, A.; Biedermann, C.; König, R.; W7-X Team

    2015-10-01

    A computer code named RayX has been developed for checking the performance of a spectroscopy system and optimizing individual parts, like detectors and filters for the pulse height analysis (PHA) diagnostic system designed for the stellarator W7-X. Using the code, the intensity and shape of the X-ray spectra are simulated for different plasma scenarios characterized by varying the temperature and density profiles as well as the electron cyclotron resonance heating (ECRH) power over a wide range. In the simulations of the recorded spectra, the influence of geometrical configuration changes of the diagnostic system (pinhole size, detector size, location of each diagnostic component), of the timing of data collection, as well as of the type and thickness of filters are being investigated. The atomic processes of free-free (bremsstrahlung), free-bound (recombination radiation), and bound-bound emission (line radiation) are considered. For the impurities fractional abundancies of 3% carbon (C), 0.5% oxygen (O) and 0.002% iron (Fe) are taken into account. Information about the number of photons which reach the detector and the current generated inside the detector is given. It is shown that the distance between pinhole and detector has a larger impact on the registered spectra (intensity and total number of photons) than the distance between plasma and pinhole. Based on the results of the simulations, the expected optimal positions of the individual components (pinholes, detectors) were defined for the PHA W7-X diagnostic system. A shorter version of this contribution is due to be published in PoS at: 1st EPS conference on Plasma Diagnostics

  16. Relative Biologic Effectiveness (RBE) of 50 kV X-rays Measured in a Phantom for Intraoperative Tumor-Bed Irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Qi; Schneider, Frank; Ma, Lin; Wenz, Frederik [Department of Radiation Oncology, Universitätsmedizin Mannheim, Medical Faculty Mannheim, University of Heidelberg, Mannheim (Germany); Herskind, Carsten, E-mail: carsten.herskind@medma.uni-heidelberg.de [Department of Radiation Oncology, Universitätsmedizin Mannheim, Medical Faculty Mannheim, University of Heidelberg, Mannheim (Germany)

    2013-03-15

    Purpose: Intraoperative radiation therapy (IORT) with low-energy x-rays is used to treat the tumor bed during breast-conserving surgery. The purpose was to determine the relative biologic effectiveness (RBE) of 50-kV x-rays for inactivation of cells irradiated in a tumor-bed phantom. Methods and Materials: The RBE was determined for clonogenic inactivation of human tumor and normal cells (MCF7, human umbilical vein endothelial cells, normal skin fibroblasts), and hamster V79 cells. The 50-kV x-rays from the Intrabeam machine (Carl Zeiss Surgical) with a spherical 4-cm applicator were used. Cells were irradiated in a water-equivalent phantom at defined distances (8.1-22.9 mm) from the applicator surface. The 50-kV x-rays from a surface therapy machine (Dermopan, Siemens) were included for comparison; 6-MV x-rays were used as reference radiation. Results: At 8.1-mm depth in the phantom (dose rate 15.1 Gy/h), mean RBE values of 50-kV x-rays from Intrabeam were 1.26 to 1.42 for the 4 cell types at doses yielding surviving fractions in the range of 0.01 to 0.5. Confidence intervals were in the range of 1.2 and 1.5. Similar RBE values were found for 50-kV x-rays from Dermopan for V79 (1.30, CI 1.25-1.36, P=.74) and GS4 (1.42, CI 1.30-1.54, P=.67). No significant dependence of RBE on dose was found for Intrabeam, but RBE decreased at a larger distance (12.7 mm; 9.8 Gy/h). Conclusions: An increased clinically relevant RBE was found for cell irradiation with Intrabeam at depths in the tumor bed targeted by IORT. The reduced RBE values at larger distances may be related to increased repair of sublethal damage during protracted irradiation or to hardening of the photon beam energy.

  17. Effect of organoclay incorporation on dental resin morphology

    International Nuclear Information System (INIS)

    Oliveira, Nadja M.S.; Reis, Romulo P.B.; Leite, Itamara F.; Morais, Crislene R.S.; Silva, Suedina M.L.

    2009-01-01

    The objective of the present work was to incorporate nanosilicates in commercial dental resins in order to prepare dental nanocomposites competitive as commercial nanoparticulates dental resins. Thus, a silicate, Cloisite 20A (C20A), was incorporated in a microhybrid dental resin (Z100) and morphological properties of the nanocomposites evaluated as a function of the incorporation method and the amount of filler employed. The samples were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The XRD results evidence that nanocomposites have been obtained and according to SEM results, the morphology of microhybrid resin was modified when C20A nanoparticulate was incorporated improve the size distribution and reduce the agglomeration of the particles. (author)

  18. 21 CFR 872.3820 - Root canal filling resin.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Root canal filling resin. 872.3820 Section 872...) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3820 Root canal filling resin. (a) Identification. A root canal filling resin is a device composed of material, such as methylmethacrylate, intended...

  19. Leaching studies on ion exchange resins immobilized in bitument matrix

    International Nuclear Information System (INIS)

    Grosche Filho, C.E.; Chandra, U.; Villalobos, J.P.

    1987-01-01

    To study radionuclide leaching from bitumen waste forms, many samples of bitumen mixed with ion-exchange resin labelled with 134 Cs were prepared. The resins used in the tests were nuclear grade mixed cationic/anionic bead resins. Different bittumen types were assayed: two destilled and to oxidized bitumens. Laboratory to scale samples, with surface/volume ratio (S/V) = 1, were molded to 5 cm diameter and 10 cm height. The composition of the mixtures were: 30, 40, 50 and 60% by weight of dried resin with bitumen. The leachant was deionized water with a leachant volume to sample surface rario of about 8 cm. Leached fractions were collected according to the recommendation of ISO method, with complete exchange of leachant beckers after each sampling. The volume collected for analysis was one liter. Marinelli were used for counting in a Ge(Li) detector. Up to now, results of 250 days have been accumulated. Samples prepared with distilled bitumen have shown a diffusion coefficient of the order of 10 -14 cm 2 /sec and those prepared with oxidized bitumen yielded a diffusion coefficient of the order of 10 -12 cm 2 /sec. Mathematical models of transport phenomena applied to cylindrical geometry were employed to fit experimental data. (Author) [pt

  20. Comparing and Optimizing Nitrate Adsorption from Aqueous Solution Using Fe/Pt Bimetallic Nanoparticles and Anion Exchange Resins

    International Nuclear Information System (INIS)

    Daud, M.; Khan, Z.; Ashgar, A.; Danish, M. I.; Qazi, I. A.

    2015-01-01

    This research work was carried out for the removal of nitrate from raw water for a drinking water supply. Nitrate is a widespread ground water contaminant. Methodology employed in this study included adsorption on metal based nanoparticles and ion exchange using anionic resins. Fe/Pt bimetallic nanoparticles were prepared in the laboratory, by the reduction of their respective salts using sodium borohydride. Scanning electron microscope, X-ray diffraction, energy dispersive spectrometry, and X-ray florescence techniques were utilized for characterization of bimetallic Fe/Pt nanoparticles. Optimum dose, ph, temperature, and contact time were determined for removal through batch tests, both for metal based nanoparticles and anionic exchange resin. Adsorption data fitted well the Langmuir isotherm and conformed to the pseudo first-order kinetic model. Results indicated 97% reduction in nitrate by 0.25 mg/L of Fe/Pt nanoparticles at ph 7 and 83% reduction in nitrate was observed using 0.50 mg/L anionic exchange resins at ph 4 and contact time of one hour. Overall, Fe/Pt bimetallic nanoparticles demonstrated greater removal efficiency due to the small particle size, extremely large surface area (627 m 2 /g), and high adsorption capacity.

  1. Completion of designing and manufacturing of the coil support structure of W7-X

    International Nuclear Information System (INIS)

    Chauvin, Didier; Koppe, Torsten; Cardella, Antonio; Missal, Bernd; Pilopp, Dirk; Di Bartolo, Giovanni; Camin, Rocio; Gonzales, Ivan; Giordano, Luca; Langone, Stefano

    2011-01-01

    In February 2000, the project called coil support structure for the Wendelstein 7-X fusion machine was started. Since October 2009 the full production of this big (80 tons) and complex component is now completed and delivered at IPP Greifswald. The W7-X coil system consists of 20 planar and 50 non-planar coils. They are supported by a pentagonal 10 m diameter, 2.5 m high called coil support structure (CSS). The CSS is divided into five modules and each module consists of two equal half modules around the radial axis. Currently, the five modules were successfully assembled with the coils meeting the tight manufacturing tolerances. Designing, structural calculation, raw material procurement, welding and soldering technologies, milling, drilling, accurate machining, helium cooling pipe forming, laser metrology, ultra sonic cleaning and vacuum test are some of the key points used all along this successful manufacturing process. The lessons learned in the large scale production of this difficult kind of support structure will be presented as relevant experience for the realization of similar systems for future fusion devices, such as ITER.

  2. Simulation of neutron fluxes around the W7-X Stellarator

    International Nuclear Information System (INIS)

    Andersson, Jenny

    1999-12-01

    A new fusion experiment, the WENDELSTEIN 7-X Stellarator (W7-X), will be undertaken in Greifswald in Germany. Measurements of the neutron flux will provide information on fusion reaction rates and possibly also on ion temperatures as function of time. For this purpose moderating neutron counters will be designed, tested, calibrated and eventually used at W7-X. Extensive Monte-Carlo simulations have been performed in order to select the most suitable detector and moderator combination with a flat response function and highest achievable efficiency. Different detector configurations with different moderating materials have been tried out, showing that a 32 cm thick graphite moderating BF 3 -counter gives the desired flat response and sufficient efficiency. Neutron spectra calculations have been made for different torus models and the influence of floor, walls and ceiling (i.e. reactor hall) have been investigated. Presented results suggest that a more detailed torus model significantly reduces the number of neutron counts at the detector. Calculations including the reactor hall indicate a tendency of shifting the neutron spectra towards the thermal region. The main part of the scattered neutrons are back-scattered from the floor. Finally, calculations on the graphite moderating BF 3 -counter in the detailed torus environment were performed in order to assess the absolute response function under the influence of the reactor hall. The results show that the detector count rate will increase by only 5-7 % when the reactor hall is taken into account. With a stellarator generating 10 12 to 10 16 neutrons per second the detector count rate will be 2x10 5 to 2x10 9 neutrons per second

  3. Simulation of neutron fluxes around the W7-X Stellarator

    Energy Technology Data Exchange (ETDEWEB)

    Andersson, Jenny

    1999-12-01

    A new fusion experiment, the WENDELSTEIN 7-X Stellarator (W7-X), will be undertaken in Greifswald in Germany. Measurements of the neutron flux will provide information on fusion reaction rates and possibly also on ion temperatures as function of time. For this purpose moderating neutron counters will be designed, tested, calibrated and eventually used at W7-X. Extensive Monte-Carlo simulations have been performed in order to select the most suitable detector and moderator combination with a flat response function and highest achievable efficiency. Different detector configurations with different moderating materials have been tried out, showing that a 32 cm thick graphite moderating BF{sub 3} -counter gives the desired flat response and sufficient efficiency. Neutron spectra calculations have been made for different torus models and the influence of floor, walls and ceiling (i.e. reactor hall) have been investigated. Presented results suggest that a more detailed torus model significantly reduces the number of neutron counts at the detector. Calculations including the reactor hall indicate a tendency of shifting the neutron spectra towards the thermal region. The main part of the scattered neutrons are back-scattered from the floor. Finally, calculations on the graphite moderating BF{sub 3} -counter in the detailed torus environment were performed in order to assess the absolute response function under the influence of the reactor hall. The results show that the detector count rate will increase by only 5-7 % when the reactor hall is taken into account. With a stellarator generating 10{sup 12} to 10{sup 16} neutrons per second the detector count rate will be 2x10{sup 5} to 2x10{sup 9} neutrons per second.

  4. Results from a search for a neutral Scalar produced in association with a W boson in p pbar collisions at squareroot s = 1.8 TeV

    International Nuclear Information System (INIS)

    Abachi, S.

    1996-08-01

    This paper presents a search for production of a hypothetical heavy particle X in association with a W boson. For the search presented here, the kinematics and acceptance are modelled under the assumption that the X particle has the spin and decay properties of the standard model Higgs boson with the modification that only X → b anti b decays are allowed. The W is required to decay via either the electron or muon mode. The complete D null 1992-1995 data set is used. This sample has an integrated luminosity of 100 pb -1 and was taken at a center of mass energy of 1.8 TeV. Limits are placed on the number of associated production events and the production cross section

  5. Experiment planning using high-level component models at W7-X

    International Nuclear Information System (INIS)

    Lewerentz, Marc; Spring, Anett; Bluhm, Torsten; Heimann, Peter; Hennig, Christine; Kühner, Georg; Kroiss, Hugo; Krom, Johannes G.; Laqua, Heike; Maier, Josef; Riemann, Heike; Schacht, Jörg; Werner, Andreas; Zilker, Manfred

    2012-01-01

    Highlights: ► Introduction of models for an abstract description of fusion experiments. ► Component models support creating feasible experiment programs at planning time. ► Component models contain knowledge about physical and technical constraints. ► Generated views on models allow to present crucial information. - Abstract: The superconducting stellarator Wendelstein 7-X (W7-X) is a fusion device, which is capable of steady state operation. Furthermore W7-X is a very complex technical system. To cope with these requirements a modular and strongly hierarchical component-based control and data acquisition system has been designed. The behavior of W7-X is characterized by thousands of technical parameters of the participating components. The intended sequential change of those parameters during an experiment is defined in an experiment program. Planning such an experiment program is a crucial and complex task. To reduce the complexity an abstract, more physics-oriented high-level layer has been introduced earlier. The so-called high-level (physics) parameters are used to encapsulate technical details. This contribution will focus on the extension of this layer to a high-level component model. It completely describes the behavior of a component for a certain period of time. It allows not only defining simple value ranges but also complex dependencies between physics parameters. This can be: dependencies within components, dependencies between components or temporal dependencies. Component models can now be analyzed to generate various views of an experiment. A first implementation of such an analyze process is already finished. A graphical preview of a planned discharge can be generated from a chronological sequence of component models. This allows physicists to survey complex planned experiment programs at a glance.

  6. 21 CFR 872.3670 - Resin impression tray material.

    Science.gov (United States)

    2010-04-01

    ... (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3670 Resin impression tray material. (a) Identification. Resin impression tray material is a device intended for use in a two-step dental mold fabricating... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Resin impression tray material. 872.3670 Section...

  7. Statistical analysis of the equilibrium configurations of the W7-X stellarator using Function Parameterization

    Energy Technology Data Exchange (ETDEWEB)

    Sengupta, A.; Geiger, J.; Mc Carthy, P. J.

    2005-07-01

    W7-X is a 5-period, fully optimised stellarator under construction at IPP-Greifswald, Germany. It has a standard magnetic configuration, with five islands at the boundary where iota=1, produced by a set of 2x5 modular field coils (MFC) in each period. The boundary iota value can be varied between 5/6 (low iota case) and 5/4 (high iota case) using 2x2 additional planar coils (PLC) per period. An important goal of W7-X is to investigate the steady state capabilities of fusion devices. For stellarators this essentially implies a real time monitoring of the discharges which have long pulse lengths, of the order of minutes. (Author)

  8. Statistical analysis of the equilibrium configurations of the W7-X stellarator using Function Parameterization

    International Nuclear Information System (INIS)

    Sengupta, A.; Geiger, J.; Mc Carthy, P. J.

    2005-01-01

    W7-X is a 5-period, fully optimised stellarator under construction at IPP-Greifswald, Germany. It has a standard magnetic configuration, with five islands at the boundary where iota=1, produced by a set of 2x5 modular field coils (MFC) in each period. The boundary iota value can be varied between 5/6 (low iota case) and 5/4 (high iota case) using 2x2 additional planar coils (PLC) per period. An important goal of W7-X is to investigate the steady state capabilities of fusion devices. For stellarators this essentially implies a real time monitoring of the discharges which have long pulse lengths, of the order of minutes. (Author)

  9. Temperature dependence of diffuse satellites in Ti–(50x)Pd–xFe (14 ⩽ x ⩽ 20 (at.%)) alloys

    International Nuclear Information System (INIS)

    Todai, Mitsuharu; Fukuda, Takashi; Kakeshita, Tomoyuki

    2014-01-01

    Highlights: • Diffuse satellites of Ti–(50x)Pd–xFe alloys have been investigated. • Diffuse satellites appear at g B2 + 〈ζζ ¯ 0〉 * below T min . • The peak position of diffuse satellites at T min agree with the length of the nesting vector. • The present result implies that the nesting effect of Fermi surface originates diffuse satellites in Ti–(50x)Pd–xFe alloys. - Abstract: Diffuse satellites appearing in electron diffraction pattern of shape memory Ti–(50x)Pd–xFe (14, 16, 18, 19 and 20, in at.%) alloys have been investigated. The satellites appear in each alloy below T min , where its electrical resistivity shows a local minimum. The positions of satellites are g B2 + 〈ζ ζ ¯ 0〉 * , where g B2 is a reciprocal lattice vector of the B2-phase. The value of ζ is smaller than 1/5 at T min for all the alloys; it increases with decreasing temperature and decreases with increasing iron content. The value of ζ at T min agrees with the length of the nesting vector previously calculated by the present authors. This result implies that Fermi surface nesting is the origin of diffuse satellites in Ti–(50x)Pd–xFe alloys

  10. Review of the acceptance tests of the W7-X superconducting magnets

    International Nuclear Information System (INIS)

    Ehmler, H.; Baldzuhn, J.; Genini, L.; Heyn, K.; Sborchia, C.; Schild, T.

    2007-01-01

    The W7-X magnet system consists of 50 non-planar coils of five different types and 20 planar coils of two different types. Factory tests of the non-planar coils are carried out at the manufacturer site of Babcock-Noell, Germany, and for the planar coils at Tesla Engineering, UK. They consist of electrical insulation checks, mass flow measurements, leak tests and sensor checks. In the test facility of CEA Saclay, France, each coil is cooled down to ∼5 K and operated at nominal current. At least one coil of each type is quenched by increasing the inlet temperature. Results of the mass flow measurements and the quench tests are presented. The manufacturing and testing progress is reviewed and the impact of technical failures is discussed. In conclusion, the scope of the tests allows a very strict quality control. This experience is highly beneficial for the construction and testing of similar components for future superconducting fusion experiments

  11. Design study of wind turbines, 50 kW to 3000 kW for electric utility applications: Executive summary

    Science.gov (United States)

    1977-01-01

    Preliminary designs of low power (50 to 500 kW) and high power (500 to 3000 kW) wind generator systems (WGS) for electric utility applications were developed. These designs provide the bases for detail design, fabrication, and experimental demonstration testing of these units at selected utility sites. Several feasible WGS configurations were evaluated, and the concept offering the lowest energy cost potential and minimum technical risk for utility applications was selected. The selected concept was optimized utilizing a parametric computer program prepared for this purpose. The utility requirements evaluation task examined the economic, operational and institutional factors affecting the WGS in a utility environment, and provided additional guidance for the preliminary design effort. Results of the conceptual design task indicated that a rotor operating at constant speed, driving an AC generator through a gear transmission is the most cost effective WGS configuration.

  12. Uranium isotope separation using styrene cation exchangers

    International Nuclear Information System (INIS)

    Kahovec, J.

    1980-01-01

    The separation of 235 U and 238 U isotopes is carried out either by simple isotope exchange in the system uranium-cation exchanger (sulphonated styrene divinylbenzene resin), or by combination of isotope exchange in a uranium-cation exchanger (Dowex 50, Amberlite IR-120) system and a chemical reaction. A review is presented of elution agents used, the degree of cation exchanger cross-linking, columns length, and 235 U enrichment. The results are described of the isotope effect study in a U(IV)-U(VI)-cation exchanger system conducted by Japanese and Romanian authors (isotope exchange kinetics, frontal analysis, reverse (indirect) frontal analysis). (H.S.)

  13. X ray spectra of X Per. [oso-8 observations

    Science.gov (United States)

    Becker, R. H.; Boldt, E. A.; Holt, S. S.; Pravdo, S. H.; Robinson-Saba, J.; Serlemitsos, P. J.; Swank, J. H.

    1978-01-01

    The cosmic X-ray spectroscopy experiment on OSO-8 observed X Per for twenty days during two observations in Feb. 1976 and Feb. 1977. The spectrum of X Per varies in phase with its 13.9 min period, hardening significantly at X-ray minimum. Unlike other X-ray binary pulsar spectra, X Per's spectra do not exhibit iron line emission or strong absorption features. The data show no evidence for a 22 hour periodicity in the X-ray intensity of X Per. These results indicate that the X-ray emission from X Per may be originating from a neutron star in a low density region far from the optically identified Be star.

  14. Ten years of cryo-magnetic W7-X test facility construction and operation

    International Nuclear Information System (INIS)

    Renard, B.; Dispau, G.; Donati, A.; Genini, L.; Gournay, J.F.; Kuster, O.; Molinie, F.; Schild, T.; Touzery, R.; Vieillard, L.; Walter, C.

    2011-01-01

    The construction, commissioning, and operation phases of the W7-X cryo-magnetic test facility in CEA Saclay lasted ten years. The large diversity of equipments called, specialties involved and problems solved attest the expertise that was required to operate the test facility and test the coils. Nearly one hundred cryogenic tests were performed on the seventy W7-X coils, at a rate always increasing, using two cryostats each holding two coils. This paper presents the test facility and its operation first, the cryogenic difficulties that were confronted with their solutions, the electro-magnetic difficulties encountered along with corrective actions, and finally the instrumentation and data acquisition aspects. (authors)

  15. Radiopacity and microhardness changes and effect of X-ray operating voltage in resin-based materials before and after the expiration date

    Directory of Open Access Journals (Sweden)

    Tirapelli Camila

    2004-01-01

    Full Text Available This study observed alteration in the radiopacity and microhardness of expired resin-based materials compared to non-expired materials and the operating characteristics of the X-ray source used. Five 2 mm-thick cured specimens were prepared for each material: composite resins (P60®, Z100®, and a compomer (Dyract AP®. Radiopacity of the specimens was evaluated comparing the density of the resin-based material to an equivalent (mm density of a 99.5% pure aluminum step wedge using a transmission densitometer. Surface microhardness measurements were carried out using a calibrated Vickers indenter on three different points of the same surface. ANOVA and Tukey tests (pre-set alpha = 0.05 revealed that expired materials showed no significant change in radiopacity. One material (Filtek P60 demonstrated lower radiopacity with lower KVp. Change in microhardness wa s statistically significant for Z100: for this material, the microhardness after expiration was significantly lower than before the expiration date.

  16. Application of neutron activation techniques and x-ray energy dispersion spectrometry, in analysis of metallic traces adsorbed by chelex-100 resin; Ativacao das tecnicas de ativacao neutronica e espectrometria por dispersao de onda e de energia de raios X, na analise de tracos metalicos adsorvidos pela resina chelex-100

    Energy Technology Data Exchange (ETDEWEB)

    Fernandes, Jair C.; Amaral, Angela M.; Magalhaes, Jesus C.; Pereira, Jose S.J.; Silva, Juliana B. da; Auler, Lucia M.L.A. [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN), Belo Horizonte, MG (Brazil)]. E-mail: jcf@urano.cdtn.br

    2000-07-01

    In this work, the authors have investigated optimal conditions of adsorption for several ion metallic groups (cations of heavy metals and transition metals, oxyanions metallics and metalloids and cations of rare earths), as traces (ppb), withdrawn and in mixture of groups, by chelex-100 resin. The experiments have been developed by bath techniques in ammonium acetate tamponade solution 40 mM pH 5,52 content 0,5 g of chelex-100 resin. After magnetic agitation for two hours, resins were dried and submitted to X-ray energy dispersion spectrometry, x-ray fluorescence spectrometry and neutron activation analysis. The results have demonstrated that chelex-100 resin adsorb quantitatively transition element groups and rare earth groups in two cases (withdrawn and simultaneously adsorption)

  17. Experimental evaluation of 8kW grid-connected photovoltaic system in Egypt

    OpenAIRE

    Elkholy, A.; Fahmy, F.H.; Abou El-Ela, A.A.; Nafeh, Abd El-Shafy A.; Spea, S.R.

    2016-01-01

    An experimental observation study of 8 kW grid-connected photovoltaic (PV) system that is installed at Electronics Research Institute (ERI), Giza, Egypt (Latitude 30.04°N, Longitude 31.21°E), is presented. This study includes the quality of the electrical power generated and injected into the network. The considered system consists of 28 × 295 Wp multicrystalline PV modules, StecaGrid three-phase 8 kW grid-connected inverter and a Solar-Log 300 PM+ for data acquisition and remote monitoring. ...

  18. Study of uranium (VI) in carbonate solution by potentiometric titrations and ion-exchange

    International Nuclear Information System (INIS)

    Billon, A.

    1968-04-01

    The present work is devoted to the fixation of uranium (VI) on the conventional anion-exchange resin Dowex 2 X 8 in carbonate and hydrogen-carbonate media. Both media were successfully used for the recuperation of uranium (VI) from very dilute solutions. Equilibrium constant of the exchange [UO 2 (CO 3 ) 3 4+ ] S + 2 [CO 3 2- ] R ↔ [UO 2 (CO 3 ) 3 4- ] R + 2[CO 3 2- ] S is determined for carbonate concentration range 0.1 M to 0.6 M from partition curves. A markedly increase in the relative fixation of uranium results with: - increasing free carbonate concentration of the solution, - decreasing uranium concentration. A study in the same conditions of the fixation of molybdenum has made it possible to separate the latter from uranium by elution, the carbonate concentration being molar. It is suggested a possibility of separation on a larger scale, based upon molybdenum displacement by uranium in hydrogen-carbonate medium. (author) [fr

  19. Oxidation of cyclic amines by molybdenum(II and tungsten(II halocarbonyls, [M(CO4X2]2 (M = Mo, W; X = Cl, Br

    Directory of Open Access Journals (Sweden)

    H.M. Mbuvi

    2013-05-01

    Full Text Available The molybdenum(II and tungsten(II halocarbonyls, [M(CO4X2]2 (M = Mo, W; X = Cl, Br react with a large excess of the nitrogen bases, 1-methylpyrrolidine, 1-methylpiperidine, 1-ethylpiperidine and 2-ethylpiperidine to give aminecarbonyl complexes of the type M(CO3L3 (L= alkylamine. Excess piperidine reacts with the tungsten halocarbonyls, [W(CO4X2]2 (X = Cl, Br, to give the trans isomer of the complex, W(CO3(C5H11N3. The halogens were recovered as the amminium salts, amine, HX. The oxidized amine dimerized to form a yellow product which was recovered as an oily liquid but in very small amounts. However, in the reaction between Mo(CO4Br2 and 1-ethylpiperidine, a yellow crystalline solid, with a melting point of 224 oC was recovered in sufficient amounts for elemental analysis, melting point and spectral data. Its mass spectrum showed a molecular ion peak at m+/z = 222, a clear evidence that the oxidized amine dimerizes. The cyclic dibasic amine piperazine, C4H10N2 is not, however, oxidized by these halocarbonyls but rather it reacts by substituting some CO groups to form products of the type, M(CO3(C4H10N22X2 (M = Mo, W; X = Cl, Br. Products were characterized by elemental analysis, IR, UV, 1H NMR and mass spectrometry.

  20. Tensile bond strength of indirect composites luted with three new self-adhesive resin cements to dentin

    Directory of Open Access Journals (Sweden)

    Cafer Türkmen

    2011-08-01

    Full Text Available OBJECTIVE: The aims of this study were to evaluate the tensile bond strengths between indirect composites and dentin of 3 recently developed self-adhesive resin cements and to determine mode of failure by SEM. MATERIAL AND METHODS: Exposed dentin surfaces of 70 mandibular third molars were used. Teeth were randomly divided into 7 groups: Group 1 (control group: direct composite resin restoration (Alert with etch-and-rinse adhesive system (Bond 1 primer/adhesive, Group 2: indirect composite restoration (Estenia luted with a resin cement (Cement-It combined with the same etch-and-rinse adhesive, Group 3: direct composite resin restoration with self-etch adhesive system (Nano-Bond, Group 4: indirect composite restoration luted with the resin cement combined with the same self-etch adhesive, Groups 5-7: indirect composite restoration luted with self-adhesive resin cements (RelyX Unicem, Maxcem, and Embrace WetBond, respectively onto the non-pretreated dentin surfaces. Tensile bond strengths of groups were tested with a universal testing machine at a constant speed of 1 mm/min using a 50 kgf load cell. Results were statistically analyzed by the Student's t-test. The failure modes of all groups were also evaluated. RESULTS: The indirect composite restorations luted with the self-adhesive resin cements (groups 5-7 showed better results compared to the other groups (p0.05. The surfaces of all debonded specimens showed evidence of both adhesive and cohesive failure. CONCLUSION: The new universal self-adhesive resins may be considered an alternative for luting indirect composite restorations onto non-pretreated dentin surfaces.

  1. Relationship between Color and Translucency of Multishaded Dental Composite Resins

    Directory of Open Access Journals (Sweden)

    Homan Naeimi Akbar

    2012-01-01

    Full Text Available The aim of the present study was to compare the translucency of different shades of two highly aesthetic multilayered restorative composite resins. In total nine shades from Esthet.X and ten shades from Filtek Supreme composite resins were chosen. Discs of each shade were prepared (N=3 and light-cured. Total and diffuse transmittance values for each sample were measured. Statistical analysis showed that the opaque dentine shades of both composites were the least translucent and the enamel shades had the highest translucency. There was a significant decrease in translucency from A2 to C2 of regular body shades and also from A4 to C4 of opaque dentine shades of Esthet.X composite resin. Grey enamel shade had a significantly higher diffuse translucency compared to clear and yellow enamel shades. There was a significant decrease in translucency from A2B to D2B and also in diffuse translucency from A4D to C6D shades of Filtek Supreme composite resin. It can be concluded that the color of the composite resins tested in this study had a significant effect on their translucency. Information on the translucency of different shades of composite resins can be very useful for the clinicians in achieving optimal esthetic restorative outcome.

  2. 1.8kW laser diode pumped YAG laser; Shutsuryoku 1.8kW no handotai laser reiki YAG laser

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1999-03-01

    Toshiba Corporation, as a participant in Ministry of International Trade and Industry`s `photon measurement and processing technology project` since August, 1997, is engaged in the development of an energy-efficient LD (laser diode) pumped semiconductor YAG (yttrium-aluminum-garnet) laser device to be used for welding and cutting. It is a 5-year project and the goal is a mean output of 10kW and efficiency of 20%. In this article, a simulation program is developed which carries out calculation about element technology items such as the tracking of the beam from the pumping LD and the excitation distribution, temperature distribution, thermal stress distribution, etc., in the YAG rod. An oscillator is constructed, based on the results of the simulation, and it exhibits a world-high class continuous laser performance of a 1.8kW output and 13% efficiency. The record of 13% efficiency is five times higher than that achieved by the conventional lamp-driven YAG laser device. (translated by NEDO)

  3. Improvement of Mechanical and Dielectric Properties of Epoxy Resin Using CNTs/ZnO Nanocomposite.

    Science.gov (United States)

    Vu, Pham Gia; Truc, Trinh Anh; Chinh, Nguyen Thuy; Tham, Do Quang; Trung, Tran Huu; Oanh, Vu Ke; Hang, To Thi Xuan; Olivier, Marjorie; Hoang, Thai

    2018-04-01

    In this study, carbon nanotubes (CNTs)/ZnO composites had been prepared using the sol-gel method and then incorporated into an epoxy resin for reinforcement of mechanical and electrical properties. Fourier Transform Infrared (FTIR), X-ray diffraction (XRD) Field Emission Scanning Electron Microscope (FE-SEM) analyses show that the ZnO nanoparticles deposited on CNTs were crystallized in a hexagonal wurtzite structure. Average particle size of ZnO deposited on the CNT was about 8 nm. The mechanical and dielectric properties of epoxy containing CNTs/ZnO were investigated in comparison to epoxy resin and epoxy resin containing only CNT or ZnO nanoparticles. The results indicated that tensile strength and elongation at break of the nanocomposite were substantially improved with the presence of CNTs/ZnO at the equal volume. The DSC analysis associate with the dielectric results shows that the behavior of epoxy/CNTs/ZnO is identical to epoxy/ZnO composite, and the CNTs is essential to the distributed arrangement of ZnO in the epoxy resin.

  4. Biphenyl liquid crystalline epoxy resin as a low-shrinkage resin-based dental restorative nanocomposite.

    Science.gov (United States)

    Hsu, Sheng-Hao; Chen, Rung-Shu; Chang, Yuan-Ling; Chen, Min-Huey; Cheng, Kuo-Chung; Su, Wei-Fang

    2012-11-01

    Low-shrinkage resin-based photocurable liquid crystalline epoxy nanocomposite has been investigated with regard to its application as a dental restoration material. The nanocomposite consists of an organic matrix and an inorganic reinforcing filler. The organic matrix is made of liquid crystalline biphenyl epoxy resin (BP), an epoxy resin consisting of cyclohexylmethyl-3,4-epoxycyclohexanecarboxylate (ECH), the photoinitiator 4-octylphenyl phenyliodonium hexafluoroantimonate and the photosensitizer champhorquinone. The inorganic filler is silica nanoparticles (∼70-100 nm). The nanoparticles were modified by an epoxy silane of γ-glycidoxypropyltrimethoxysilane to be compatible with the organic matrix and to chemically bond with the organic matrix after photo curing. By incorporating the BP liquid crystalline (LC) epoxy resin into conventional ECH epoxy resin, the nanocomposite has improved hardness, flexural modulus, water absorption and coefficient of thermal expansion. Although the incorporation of silica filler may dilute the reinforcing effect of crystalline BP, a high silica filler content (∼42 vol.%) was found to increase the physical and chemical properties of the nanocomposite due to the formation of unique microstructures. The microstructure of nanoparticle embedded layers was observed in the nanocomposite using scanning and transmission electron microscopy. This unique microstructure indicates that the crystalline BP and nanoparticles support each other and result in outstanding mechanical properties. The crystalline BP in the LC epoxy resin-based nanocomposite was partially melted during exothermic photopolymerization, and the resin expanded via an order-to-disorder transition. Thus, the post-gelation shrinkage of the LC epoxy resin-based nanocomposite is greatly reduced, ∼50.6% less than in commercialized methacrylate resin-based composites. This LC epoxy nanocomposite demonstrates good physical and chemical properties and good biocompatibility

  5. Preparation of Zr50Al15− xNi10Cu25Yx amorphous powders by ...

    Indian Academy of Sciences (India)

    The as-milled powders were characterized by X-ray diffraction and transmission electron microscopy. The results show that partial substitution of Al by Y can improve the glass-forming ability of Zr50Al15Ni10Cu25 alloy. Thermodynamic calculation of equivalent free energy shows that Zr50Al13.8Ni10Cu25Y1.2 alloy has the ...

  6. Cytotoxicity Comparison of Harvard Zinc Phosphate Cement Versus Panavia F2 and Rely X Plus Resin Cements on Rat L929-fibroblasts.

    Science.gov (United States)

    Mahasti, Sahabi; Sattari, Mandana; Romoozi, Elham; Akbar-Zadeh Baghban, Alireza

    2011-01-01

    Resin cements, regardless of their biocompatibility, have been widely used in restorative dentistry during the recent years. These cements contain hydroxy ethyl methacrylate (HEMA) molecules which are claimed to penetrate into dentinal tubules and may affect dental pulp. Since tooth preparation for metal ceramic restorations involves a large surface of the tooth, cytotoxicity of these cements would be more important in fixed prosthodontic treatments. The purpose of this study was to compare the cytotoxicity of two resin cements (Panavia F2 and Rely X Plus) versus zinc phosphate cement (Harvard) using rat L929-fibroblasts in vitro. In this experimental study, ninety hollow glass cylinders (internal diameter 5-mm, height 2-mm) were made and divided into three groups. Each group was filled with one of three experimental cements; Harvard Zinc Phosphate cement, Panavia F2 resin cement and Rely X Plus resin cement. L929- Fibroblast were passaged and subsequently cultured in 6-well plates of 5×10(5) cells each. The culture medium was RPMI_ 1640. All samples were incubated in CO2. Using enzyme-linked immune-sorbent assay (ELISA) and (3-(4,5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide) (MTT) assay, the cytotoxicity of the cements was investigated at 1 hour, 24 hours and one week post exposure. Statistical analyses were performed via two-way ANOVA and honestly significant difference (HSD) Tukey tests. This study revealed significant differences between the three cements at the different time intervals. Harvard cement displayed the greatest cytotoxicity at all three intervals. After 1 hour Panavia F2 showed the next greatest cytotoxicity, but after 24-hours and oneweek intervals Rely X Plus showed the next greatest cytotoxicity. The results further showed that cytotoxicity decreased significantly in the Panavia F2 group with time (pHarvard cement group failed to showed no noticeable change in cytotoxicity with time. Although this study has limitations, it provides

  7. Immobilisation of ion exchange resins in cement

    International Nuclear Information System (INIS)

    Howard, C.G.; Jolliffe, C.B.; Lee, D.J.

    1990-02-01

    Over the last seven years, Low Oxidation State Metal Ion reagents (LOMI) have been used to decontaminate the 100 MW(e) Steam Generating Heavy Water Ractor (SGHWR) at Winfrith. The use of these reagents has resulted in a dilute ionic solution containing activation products which are produced by corrosion of metallic components in the reactor. It has been demonstrated that the amount of activity in the solution can be reduced using organic ion exchanger resins. These resins consist of a cross linked polystyrene with sulphonic acid or quaternary ammonium function groups and can be successfully immobilised in blended cement systems. The formulation which has been developed is produced from a 9 to 1 blend of ground granulated blast furnace slag (BFS) and ordinary Portland cement (OPC) containing 28% ion exchange resin in the water saturated form. If 6% Microsilica is added to the blended cement the waste loading can be increased to 36 w/o. (author)

  8. Highly hydrated poly(allylamine)/silica magnetic resin

    International Nuclear Information System (INIS)

    Johnson, Andrew K.; Kaczor, Jozef; Han, Hongmei; Kaur, Maninder; Tian, Guoxin; Rao, Linfeng; Qiang, You; Paszczynski, Andrzej J.

    2011-01-01

    The creation of multifunctional nanomaterials by combining organic and inorganic components is a growing trend in nanoscience. The unique size-dependent properties of magnetic nanoparticles (MNPs) make them amenable to numerous applications such as carriers of expensive biological catalysts, in magnetically assisted chemical separation of heavy metals and radionuclides from contaminated water sources. The separation of minor actinides from high-level radionuclide waste requires a sorbent stable in acidic pH, with ease of surface functionalization, and a high capacity for binding the molecules of interest. For the described experiments, the MNPs with 50 nm average size were used (size distribution from 20 to 100 nm and an iron content of 80–90 w/w%). The MNPs that have been double coated with an initial silica coating for protection against iron solubilization and oxidation in nitric acid solution (pH 1) and a second silica/polymer composite coating incorporating partially imbedded poly(allylamine) (PA). The final product is magnetic, highly swelling, containing >95% water, with >0.5 mmol amines g −1 available for functionalization. The amine groups of the magnetic resin were functionalized with the chelating molecules diethylenetriaminepentaacetic acid (DTPA) and N,N-dimethyl-3-oxa-glutaramic acid (DMOGA) for separation of minor actinides from used nuclear fuel.

  9. A new ion selective electrode for cesium (I) based on calix[4]arene-crown-6 compounds.

    Science.gov (United States)

    Ramanjaneyulu, P S; Kumar, Abha Naveen; Sayi, Y S; Ramakumar, K L; Nayak, S K; Chattopadhyay, S

    2012-02-29

    A polyvinylchloride (PVC) based liquid membrane ion selective electrode (ISE) for cesium has been developed. 25,27-Dihydroxycalix[4]arene-crown-6 (L1), 5,11,17,23-tetra-tert-butyl-25,27-dimethoxycalix[4]arene-crown-6 (L2) and 25,27-bis(1-octyloxy)calix[4]arene-crown-6 (L3) were investigated for their use as ionophores. The cation exchange resin DOWEX-50W was used to maintain low activity Cs+ in inner filling solution to improve the performance. The best response for cesium was observed with L3 along with optimized membrane constituents and composition. Excellent Nernstian response (56.6 mV/decade of Cs(I)) over the concentration range 10(-7) to 10(-2)M of Cs(I) was obtained with a fast response time of less than 10s. Detection limit for Cs(I) using the present ISE is 8.48×10(-8) M Cs(I). Separate solution method (SSM) was applied to ascertain the selectivity for Cs(I) over alkali, alkaline earth and transition metal ions. The response of ISE for Cs(I) was fairly constant over the pH range of 4-11. The lifetime of the electrode is 10 months which is the highest life for any membrane based Cs-ISE so far developed. The concentration of cesium ion in two simulated high level active waste streams was determined and results agreed well with those obtained independently employing AAS. Copyright © 2011 Elsevier B.V. All rights reserved.

  10. Shimadzu magnetic resonance imaging system, SMT-50X

    International Nuclear Information System (INIS)

    Kohno, Kazuhiro; Yamauchi, Mikio; Shimizu, Koji; Fujio, Yasuo

    1990-01-01

    We have already had the passage of five years, since 0.5 T MRI system named SMT-50A had been announced. On the other hand, many severe efforts in the fields of both technic and diagnosis have been done to get higher image quality having more informations and they caused recent abrupt progress in MRI. To reply these demands, we have developed new 0.5T super-conductive MRI system 'SMT-50X', having the following features in the points of image quality, operability and economy. (1) RF antenna, called multipolarization has been developed. (2) Compact gantry having a large bore size has been designed for patient to get enough view in it. (3) Easier operation could be done by means of multitask software system. This paper introduces the outline, features and clinical images acquired by SMT-50X. (author)

  11. DISCOVERY OF X-RAY EMISSION FROM AND DISTANCE TO THE SUPERNOVA REMNANT G84.2-0.8

    Energy Technology Data Exchange (ETDEWEB)

    Leahy, Denis A.; Green, Kaylie S., E-mail: leahy@ucalgary.ca, E-mail: ksgreen@ucalgary.ca [Department of Physics and Astronomy, University of Calgary, Calgary, Alberta, T2N 1N4 (Canada)

    2012-11-20

    We analyze X-ray and radio observations of the supernova remnant G84.2-0.8. 1420 MHz atomic hydrogen (H I) line and radio continuum data yield H I absorption spectra and a new H I absorption distance of 5.8-6.2 kpc. Archival X-ray observations from ROSAT and Chandra which cover the area including G84.2-0.8 are analyzed to show extended X-ray emission from G84.2-0.8. Fits to X-ray spectra from Chandra, with the new H I distance of 5.8-6.2 kpc, are used to determine the Sedov parameters of the supernova remnant. G84.2-0.8 is large (16-18 pc radius), middle aged ({approx}9000 yr), expanding in low-density interstellar medium (0.02 cm{sup -3}), and consistent with a low explosion energy (0.8-6.5 Multiplication-Sign 10{sup 50} erg).

  12. Thermal conductivity and Kapitza resistance of epoxy resin fiberglass tape at superfluid helium temperature

    Science.gov (United States)

    Baudouy, B.; Polinski, J.

    2009-03-01

    The system of materials composed of fiberglass epoxy resin impregnated tape constitutes in many cases the electrical insulation for "dry"-type superconducting accelerator magnet such as Nb 3Sn magnets. Nb 3Sn magnet technology is still under development in a few programs to reach higher magnetic fields than what NbTi magnets can produce. The European program, Next European Dipole (NED), is one of such programs and it aims to develop and construct a 15 T class Nb 3Sn magnet mainly for upgrading the Large Hardron Collider. Superfluid helium is considered as one possible coolant and since the magnet has been designed with a "dry" insulation, the thermal conductivity and the Kapitza resistance of the electrical insulation are the key properties that must be know for the thermal design of such a magnet. Accordingly, property measurements of the epoxy resin fiberglass tape insulation system developed for the NED project was carried out in superfluid helium. Four sheets with thicknesses varying from 40 to 300 μm have been tested in a steady-state condition. The determined thermal conductivity, k, is [(25.8 ± 2.8) · T - (12.2 ± 4.9)] × 10 -3 W m -1 K -1 and the Kapitza resistance is given by R K = (1462 ± 345) · T(-1.86 ± 0.41) × 10 -6 Km 2 W -1 in the temperature range of 1.55-2.05 K.

  13. Surface roughness of etched composite resin in light of composite repair

    NARCIS (Netherlands)

    Loomans, B.A.C.; Cardoso, M.V.; Opdam, N.J.M.; Roeters, F.J.M.; Munck, J. De; Huysmans, M.C.D.N.J.M.; Meerbeek, B. Van

    2011-01-01

    OBJECTIVES: In search for clinically effective composite repair protocols, the effect of various etching protocols on the surface roughness of composite resins with different filler composition were investigated. METHODS: Of two composite resins (hybrid-filled Clearfil AP-X; nano-filled Filtek

  14. Fabrication and testing of W7-X pre-series target elements

    International Nuclear Information System (INIS)

    Boscary, J; Boeswirth, B; Greuner, H; Grigull, P; Missirlian, M; Plankensteiner, A; Schedler, B; Friedrich, T; Schlosser, J; Streibl, B; Traxler, H

    2007-01-01

    The assembly of the highly-loaded target plates of the WENDELSTEIN 7-X (W7-X) divertor requires the fabrication of 890 target elements (TEs). The plasma facing material is made of CFC NB31 flat tiles bonded to a CuCrZr copper alloy water-cooled heat sink. The elements are designed to remove a stationary heat flux and power up to 10 MW m -2 and 100 kW, respectively. Before launching the serial fabrication, pre-series activities aimed at qualifying the design, the manufacturing route and the non-destructive examinations (NDEs). High heat flux (HHF) tests performed on full-scale pre-series TEs resulted in an improvement of the design of the bond between tiles and heat sink to reduce the stresses during operation. The consequence is the fabrication of additional pre-series TEs to be tested in the HHF facility GLADIS. NDEs of this bond based on thermography methods are developed to define the acceptance criteria suitable for serial fabrication

  15. On the structural and magnetic properties of amorphous Fe84-xWxB16 alloys in dependence of W content

    International Nuclear Information System (INIS)

    Novakova, A.A.; Sidorova, G.V.; Katsnelson, A.A.; Szasz, A.; Kojnok, J.

    1990-01-01

    A series of rapidly solidificated amorphous Fe 84-x W x B 16 (x=0-5) alloys have been studied. A strictly linear decrease of H eff versus concentration of W has been observed by Moessbauer spectroscopy. (orig.)

  16. High Power (50W) WDM Space Lasercom 1.5um Fiber Laser Transmitter, Phase I

    Data.gov (United States)

    National Aeronautics and Space Administration — Fibertek proposes to develop and demonstrate a spaceflight prototype of a wideband, high power (up to 50W), polarization maintaining (PM), 1.5-um fiber laser...

  17. Synthesis, X-ray structure, and hydrolytic chemistry of the high potent antiviral polyniobotungstate A-[alpha]-[Si2Nb6W18O77]8

    Science.gov (United States)

    Gyu-Shik Kim; Huadong Zeng; Jeffrey T. Rhule; Ira A. Weinstock; Craig L. Hill

    1999-01-01

    Potently antiviral polyniobotungstates have been structurally characterized; the dimer A-[alpha]-[Si2Nb6W18O77]8– cleaves cleanly to the monomer A-[alpha]-[SiNb3W9O40]7– within 1 min in aqueous solution buffered at physiological (neutral) pH establishing that the monomer and not the dimer is pharmacologically relevant.

  18. Dowex anion exchanger-loaded-baker's yeast as bi-functionalized biosorbents for selective extraction of anionic and cationic mercury(II) species

    International Nuclear Information System (INIS)

    Mahmoud, Mohamed E.; Yakout, Amr A.; Osman, Maher M.

    2009-01-01

    Dowex anion exchanger-immobilized-baker's yeast [Dae-yeast] were synthesized and potentially applied as environmental friendly biosorbents to evaluate the up-take process of anionic and cationic mercury(II) species as well as other metal ions. Optimization of mass ratio of Dowex anion exchanger versus yeast (1:1-1:10) in presence of various interacting buffer solutions (pH 4.0-9.0) was performed and evaluated. Surface modification of [Dae-yeast] was characterized by scanning electron microscopy (SEM) and infrared spectroscopy. The maximum metal biosorption capacity values of [Dae-yeast] towards mercury(II) were found in the range of 0.800-0.960, 0.840-0.950 and 0.730-0.900 mmol g -1 in presence of buffer solutions pH 2.0, 4.0 and 7.0, respectively. Three possible and different mechanisms are proposed to account for the biosorption of mercury and mercuric species under these three buffering conditions based on ion exchange, ion pair and chelation interaction processes. Factors affecting biosorption of mercury from aqueous medium including the pH effect of aqueous solutions (1.0-7.0), shaking time (1-30 min) and interfering ions were searched. The potential applications of modified biosorbents for selective biosorption and extraction of mercury from different real matrices including dental filling waste materials, industrial waste water samples and mercury lamp waste materials were also explored. The results denote to excellent percentage extraction values, from nitric acid as the dissolution solvent with a pH 2.0, as determined in the range of 90.77-97.91 ± 3.00-5.00%, 90.00-93.40 ± 4.00-5.00% and 92.31-100.00 ± 3.00-4.00% for the three tested samples, respectively.

  19. Preparation of nanocomposites resin from seed Pterodon emarginatus doped maghemite nanoparticles.

    Science.gov (United States)

    Silveira, L B; Martins, Q S; Maia, J C; Santos, J G

    2012-06-01

    Electrical characterization and magnetic nanocomposite resin seeds Pterodon emarginatus (PE) doped with nanoparticles of maghemite and treated by different chemical processes is reported in this paper. The pure PE resin showed semiconducting characteristics probably the presence of natural iron oxide in its molecular structure. The analysis of Mössbauer spectra pure resin showed two magnetic sites presented on measurements made at temperature of 300 K. Six "LEDs" to have been doped maghemite nanoparticles forming concentrations of 2.6 x 10(15) to 1.56 x 10(16) particles/cm2 forming the LED-PEMN. In the presence of the applied current versus voltage (0 to 0.9 V) LED-PEMN shown semiconducting properties. In the presence of frequency versus voltage sample of pure resin and LED features small decrease. While samples of LED-PEMN suffers loss frequency linearly with concentration and voltage. The pure PE resin shows high resistance to the applied voltage while the LED-PEMN is observed linear increase with the strength and concentration of nanoparticles of maghemite.

  20. Solidification of radioactive wastes with thermosetting resin

    International Nuclear Information System (INIS)

    Hayashi, M.; Kobayashi, K.; Okamoto, O.; Kagawa, T.; Wakamatsu, K.; Irie, H.; Matsuura, H.; Yasumura, K.; Nakayama, Y.

    1982-01-01

    Dried simulated radioactive wastes were solidified with thermosetting resin and their properties were investigated with laboratory scale and real scale products through extensive testings, such as mechanical resistance, resistance to leaching and swelling in water, radiation resistance, fire resistance and resistance to temperature cycling. The typical results were as follows: over 600 kg/cm 2 of compressive strength, diffusion constant of approx. 10 - 5 cm 2 /day for 137 Cs leaching from solidified waste products, no significant change was found for up to 5 x 10 8 RAD irradiation, and damages were limited to the surface of the products after the thermal test and dropping impact test. 7 figures, 4 tables

  1. Composition analysis of Ta-W alloy using NAA and EDXRF techniques

    International Nuclear Information System (INIS)

    Swain, K.K.; Remya Devi, P.S.; Chavan, Trupti A.; Verma, R.; Reddy, A.V.R.

    2015-01-01

    Tantalum-Tungsten (Ta-W) alloy is a high strength alloy and is used in corrosion resistant chemical process equipment's including heat exchangers, condensers, heating and cooling coils and reaction vessels. Ta-W alloy is also used as ion extraction plate during laser Isotope separation of uranium and hence the composition is critical for its optimal application. The composition of the alloy was determined by neutron activation analysis (NAA) and energy dispersive X-ray fluorescence spectrometry (EDXRF) techniques. Ta-W alloy sample was received from Nuclear Fuel Complex (NFC), Hyderabad. For NAA, samples (50 - 500 mg) were sealed in polyethylene. High purity Ta foil (30 - 40 mg) and W foil (10 - 20 mg) were packed and used as comparators. Samples and standards were irradiated in the graphite reflector position of Advanced Heavy Water Reactor Critical Facility (AHWR CF) reactor, BARC, Mumbai for 4 hours. After suitable decay period, radioactivity assay was carried out using a 45% relative efficiency high purity germanium (HPGe) detector coupled to MCA with 8 k conversion gain

  2. Effect of prophylactic polishing protocols on the surface roughness of esthetic restorative materials.

    Science.gov (United States)

    Neme, A L; Frazier, K B; Roeder, L B; Debner, T L

    2002-01-01

    Many polishing protocols have been evaluated in vitro for their effect on the surface roughness of restorative materials. These results have been useful in establishing protocols for in vivo application. However, limited research has focused on the subsequent care and maintenance of esthetic restorations following their placement. This investigation evaluated the effect of five polishing protocols that could be implemented at recall on the surface roughness of five direct esthetic restorative materials. Specimens (n=25) measuring 8 mm diameter x 3 mm thick were fabricated in an acrylic mold using five light-cured resin-based materials (hybrid composite, microfilled composite, packable composite, compomer and resin-modified glass ionomer). After photopolymerization, all specimens were polished with Sof-Lex Disks to produce an initial (baseline) surface finish. All specimens were then polished with one of five prophylactic protocols (Butler medium paste, Butler coarse paste, OneGloss, SuperBuff or OneGloss & SuperBuff). The average surface roughness of each treated specimen was determined from three measurements with a profilometer (Surface 1). Next, all specimens were brushed 60,000 times at 1.5 Hz using a brush-head force of 2 N on a Manly V-8 cross-brushing machine in a 50:50 (w/w) slurry of toothpaste and water. The surface roughness of each specimen was measured after brushing (Surface 2) followed by re-polishing with one of five protocols, then final surface roughness values were determined (Surface 3). The data were analyzed using repeated measures ANOVA. Significant differences (p=0.05) in surface roughness were observed among restorative materials and polishing protocols. The microfilled and hybrid resin composite yielded significantly rougher surfaces than the other three materials following tooth brushing. Prophylactic polishing protocols can be used to restore a smooth surface on resin-based esthetic restorative materials following simulated tooth

  3. Creating subgroups of U(2w) for quantum-minus computers

    International Nuclear Information System (INIS)

    De Vos, Alexis; Boes, Michiel

    2011-01-01

    Classical reversible computers on w bits are isomorphic to the (finite) symmetric group S 2 w ; quantum computers on w qubits are isomorphic to the (Lie) unitary group U(2 w ). We investigate and classify groups X which represent computers intermediate between classical reversible computers and quantum computers. Such intermediate groups X may exist in three flavours: - finite groups of order larger than (2 w )!,; - infinite but discrete groups, and; - Lie groups of dimension smaller than (2 w ). The larger the group, the more powerful the computer may be, but the smaller the group, the easier it can be to build the computer hardware. In the present paper, we investigate the first two flavours only. For our purpose, we start from 1-qubit transformations, represented by 2 x 2 unitary matrices. We call this group the creator. Its members are called gates and act on one qubit. Controlled gates are quantum circuits acting on w qubits, such that the 1-qubit transformation (applied to a particular qubit) depends on the state of the w - 1 other qubits. The controlled gates generate the group X of 2 w x 2 w matrices, called the creation. We discuss all creators of order up to 8. Additionally a creator of order 16 and one of order 192 are discussed.

  4. 50 CFR 600.345 - National Standard 8-Communities.

    Science.gov (United States)

    2010-10-01

    ... 50 Wildlife and Fisheries 8 2010-10-01 2010-10-01 false National Standard 8-Communities. 600.345....345 National Standard 8—Communities. (a) Standard 8. Conservation and management measures shall... overfishing and rebuilding of overfished stocks), take into account the importance of fishery resources to...

  5. High thermal stability in W/MgO/CoFeB/W/CoFeB/W stacks via ultrathin W insertion with perpendicular magnetic anisotropy

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Yi; Yu, Tao [School of Physics and Nuclear Energy Engineering, Beihang University, Beijing 100191 (China); Zhu, Zhengyong; Zhong, Huicai [Institute of Microelectronics, Chinese Academy of Sciences, Beijing 100029 (China); Khamis, Khamis Masoud [School of Physics and Nuclear Energy Engineering, Beihang University, Beijing 100191 (China); Zhu, Kaigui, E-mail: kgzhu@buaa.edu.cn [School of Physics and Nuclear Energy Engineering, Beihang University, Beijing 100191 (China); Key Laboratory of Micro-Nano Measurement-Manipulation and Physics, Ministry of Education, Beihang University, Beijing 100191 (China)

    2016-07-15

    The perpendicular magnetic anisotropy (PMA) of a series of top MgO/CoFeB/W stacks were studied. In these stacks, the thickness of CoFeB is limited in a range of 1.1–2.2 nm. It was found that the stack can still maintain PMA in a 1.9 nm thick CoFeB free layer. Besides, we investigated the thermal stability factor ∆ of a spin transfer torque magnetic random access memory (STT-MRAM) by inserting an ultra-thin W film of 0.8 nm between two CoFeB films. The result shows a clear PMA behavior for the samples with CoFeB thickness up to 2.5 nm, and an in-plane magnetic anisotropy (IMA) when the CoFeB is thicker than 2.5 nm. Moreover, the thermal stability factor ∆ of the CoFeB stack with W insertion is about 132 for a 50 nm size STT-MRAM device, which is remarkably improved compared to 112 for a sample without W insertion. Our results represent an alternative way to realize the endurance at high annealing temperature, high-density and high ∆ in STT-MRAM device by ultra-thin W insertion. - Highlights: • The MgO/CoFeB/W multilayer can still maintain PMA in a CoFeB thickness of 1.9 nm. • The sample with 2.5 nm thickness of CoFeB by W insertion can still maintain PMA. • The sample with W insertion can still maintain PMA until the annealing temperature as high as 350 °C. • The thermal stability factor ∆ of sample with W insertion could be increase to about 132 for a 50 nm size STT-MRAM device.

  6. 21 CFR 872.3300 - Hydrophilic resin coating for dentures.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Hydrophilic resin coating for dentures. 872.3300... (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3300 Hydrophilic resin coating for dentures. (a) Identification. A hydrophilic resin coating for dentures is a device that consists of a water...

  7. 21 CFR 872.3310 - Coating material for resin fillings.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Coating material for resin fillings. 872.3310... (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3310 Coating material for resin fillings. (a) Identification. A coating material for resin fillings is a device intended to be applied to the...

  8. CURING OF POLYMERIC COMPOSITES USING MICROWAVE RESIN TRANSFER MOULDING (RTM

    Directory of Open Access Journals (Sweden)

    R. YUSOFF

    2007-08-01

    Full Text Available The main objective of this work is to compare the difference between microwave heating and conventional thermal heating in fabricating carbon/epoxy composites. Two types of epoxy resin systems were used as matrices, LY5052-HY5052 and DGEBA-HY917-DY073. All composite samples were fabricated using resin transfer moulding (RTM technique. The curing of the LY5052-HY5052-carbon and the DGEBA-HY917-DY073-carbon composite systems, were carried out at 100 °C and 120 °C, respectively. Microwave heating showed better temperature control than conventional heating, however, the heating rate of the microwave cured samples were slower than the conventionally cured samples. This was attributed to the lower power (250 W used when heating with microwaves compared to 2000 W used in conventional heating. Study of thermal characteristics as curing progressed showed that the polymerisation reaction occurred at a faster rate during microwave curing than in conventional curing for both the DGEBA and the LY/HY5052 carbon composite systems. The actual cure cycle was reduced from 60 minutes to 40 minutes when using microwaves for curing DGEBA-carbon composites. As for LY/HY5052-carbon composites, the actual cure cycle was reduced from 3 hours to 40 minutes. Both conventional and microwave heating yielded similar glass transition temperatures (120 °C for DGEBA systems and 130 °C for LY/HY5052 systems. Microwave cured composites had higher void contents than conventionally cured composites (2.2-2.8% and 1.8-2.4% for DGEBA and LY/HY5052 microwave cured composites, respectively, compared to 0.2-0.4% for both DGEBA and LY/HY5052 thermally cured composites. C-scan traces showed that all composites, regardless of methods of curing, had minimal defects.

  9. Influence of artificial accelerated aging on dimensional stability of acrylic resins submitted to different storage protocols.

    Science.gov (United States)

    Garcia, Lucas da Fonseca Roberti; Roselino, Lourenço de Moraes Rego; Mundim, Fabrício Mariano; Pires-de-Souza, Fernanda de Carvalho Panzeri; Consani, Simonides

    2010-08-01

    The aim of this study was to evaluate the influence of artificial accelerated aging on dimensional stability of two types of acrylic resins (thermally and chemically activated) submitted to different protocols of storage. One hundred specimens were made using a Teflon matrix (1.5 cm x 0.5 mm) with four imprint marks, following the lost-wax casting method. The specimens were divided into ten groups, according to the type of acrylic resin, aging procedure, and storage protocol (30 days). GI: acrylic resins thermally activated, aging, storage in artificial saliva for 16 hours, distilled water for 8 hours; GII: thermal, aging, artificial saliva for 16 hours, dry for 8 hours; GIII: thermal, no aging, artificial saliva for 16 hours, distilled water for 8 hours, GIV: thermal, no aging, artificial saliva for 16 hours, dry for 8 hours; GV: acrylic resins chemically activated, aging, artificial saliva for 16 hours, distilled water for 8 hours; GVI: chemical, aging, artificial saliva for 16 hours, dry for 8 hours; GVII: chemical, no aging, artificial saliva for 16 hours, distilled water for 8 hours; GVIII: chemical, no aging, artificial saliva for 16 hours, dry for 8 hours GIX: thermal, dry for 24 hours; and GX: chemical, dry for 24 hours. All specimens were photographed before and after treatment, and the images were evaluated by software (UTHSCSA - Image Tool) that made distance measurements between the marks in the specimens (mm), calculating the dimensional stability. Data were submitted to statistical analysis (two-way ANOVA, Tukey test, p= 0.05). Statistical analysis showed that the specimens submitted to storage in water presented the largest distance between both axes (major and minor), statistically different (p artificial accelerated aging and storage period influenced these alterations.

  10. Microwave absorption properties of barium titanate/epoxide resin composites

    International Nuclear Information System (INIS)

    Chen Xiaodong; Wang Guiqin; Duan Yuping; Liu Shunhua

    2007-01-01

    Nano-barium titanate (BT) was prepared by a sol-gel method. The prepared powders were characterized by x-ray powder diffraction and transmission electron microscopy. The complex relative dielectric permittivity (ε = ε' - jε-prime) and magnetic permeability (μ = μ' - jμ-prime) of the BT powders were measured in the frequency range 8 ∼ 18 GHz. The BT/epoxide resin (EP) composite with different volume contents was investigated. The effects of thickness on the BT/EP composite were studied. It was found that an optimum thickness and contents of the absorber can yield the maximum reflection loss which could be obtained over a broad frequency region in the X and Ku bands. Our results indicate that BT could be a promising microwave absorption material

  11. Atomic hydrogen in and around the giant molecular cloud near W3 and W4

    International Nuclear Information System (INIS)

    Hasegawa, T.; Sato, F.; Fukui, Y.

    1980-01-01

    Cold HI gas appears as self-absorption dips in the 21-cm line profiles in and around the giant molecular cloud near W3 and W4. The cold HI cloud is approximately 150 pc long and extends along the galactic plane. It consists of several fragments, each of which is typically approximately 25 pc in diameter and (1 - 4) X 10 4 solar masses. The [H 2 ]/[HI] ratio is estimated to be 15 - 50. The mass of the entire HI cloud amounts to approximately 10 5 solar masses which is comparable to that observed in CO emission. (Auth.)

  12. The Malarial Exported PFA0660w Is an Hsp40 Co-Chaperone of PfHsp70-x.

    Directory of Open Access Journals (Sweden)

    Michael O Daniyan

    Full Text Available Plasmodium falciparum, the human pathogen responsible for the most dangerous malaria infection, survives and develops in mature erythrocytes through the export of proteins needed for remodelling of the host cell. Molecular chaperones of the heat shock protein (Hsp family are prominent members of the exportome, including a number of Hsp40s and a Hsp70. PFA0660w, a type II Hsp40, has been shown to be exported and possibly form a complex with PfHsp70-x in the infected erythrocyte cytosol. However, the chaperone properties of PFA0660w and its interaction with human and parasite Hsp70s are yet to be investigated. Recombinant PFA0660w was found to exist as a monomer in solution, and was able to significantly stimulate the ATPase activity of PfHsp70-x but not that of a second plasmodial Hsp70 (PfHsp70-1 or a human Hsp70 (HSPA1A, indicating a potential specific functional partnership with PfHsp70-x. Protein binding studies in the presence and absence of ATP suggested that the interaction of PFA0660w with PfHsp70-x most likely represented a co-chaperone/chaperone interaction. Also, PFA0660w alone produced a concentration-dependent suppression of rhodanese aggregation, demonstrating its chaperone properties. Overall, we have provided the first biochemical evidence for the possible role of PFA0660w as a chaperone and as co-chaperone of PfHsp70-x. We propose that these chaperones boost the chaperone power of the infected erythrocyte, enabling successful protein trafficking and folding, and thereby making a fundamental contribution to the pathology of malaria.

  13. Investigation of Resin Systems for Improved Ablative Materials

    Science.gov (United States)

    1966-04-01

    condensed rings, Boron linear chain of rings Carboranes B-P Resins Polymers Containing Si-O Silicon Si -C Si -N Furan Derivatives Furfural Base Furfural ...8217 Adsorption Theory of Adhesion’ presented at the 144th American Chemical Society Meeting, held in Los Angeles, April 1963. 15. Freeman, J. H. , L. W

  14. 21 CFR 872.3770 - Temporary crown and bridge resin.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Temporary crown and bridge resin. 872.3770 Section... (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3770 Temporary crown and bridge resin. (a) Identification. A temporary crown and bridge resin is a device composed of a material, such as...

  15. Solid-state synthesis in the system Na0.8NbyW1-yO3 with 0≤y≤0.4: A new phase, Na0.5NbO2.75, with perovskite-type structure

    International Nuclear Information System (INIS)

    Debnath, Tapas; Ruescher, Claus H.; Gesing, Thorsten M.; Koepke, Juergen; Hussain, Altaf

    2008-01-01

    Series of compounds in the system Na x Nb y W 1-y O 3 were prepared according to the appropriate molar ratio of Na 2 WO 4 , WO 3 , WO 2 and Nb 2 O 5 with x=0.80 and 0.0≤y≤0.4 at 600 deg. C in evacuated silica glass tubes. These compounds were investigated by X-ray powder diffraction, optical microscopy, microprobe analysis, Raman and optical microspectroscopy. A y-dependent separation into three distinct coloured crystallites with cubic perovskite-type structures is observed: (i) red-orange crystallites with composition Na x WO 3 with slightly decreasing x (i.e. 0.8-0.72) with increasing nominal y, (ii) bluish solid solution of composition Na x Nb y W 1-y O 3 and (iii) white crystallites of a new phase having defect perovskite-type structure with composition Na 0.5 NbO 2.75 . - Graphical abstract: Optical micrograph of a polished sample of nominal composition Na 0.8 Nb 0.4 W 0.6 O 3 showing a mixture of three different coloured crystals: red, light blue and white. The scale bar is 30 μm

  16. Direct spectrometry: a new alternative for measuring the fluorescence of composite resins and dental tissues.

    Science.gov (United States)

    da Silva, Tm; de Oliveira, Hpm; Severino, D; Balducci, I; Huhtala, Mfrl; Gonçalves, Sep

    2014-01-01

    The aim of this study was to evaluate the fluorescence intensity of different composite resins and compare those values with the fluorescence intensity of dental tissues. Different composite resins were used to make 10 discs (2 mm in depth and 4 mm in diameter) of each brand, divided into groups: 1) Z (Filtek Z350, 3M ESPE), 2) ES (Esthet-X, Dentsply), 3) A (Amelogen Plus, Ultradent), 4) DVS (Durafill-VS, Heraeus Kulzer) with 2 mm composite resin for enamel (A2), 5) OES ([Esthet-X] opaque-OA [1 mm] + enamel-A2 [1 mm]); 6) ODVSI ([Charisma-Opal/Durafill-VSI], opaque-OM (1 mm) + translucent [1mm]), and 7) DVSI ([Durafill- VSI] translucent [2 mm]). Dental tissue specimens were obtained from human anterior teeth cut in a mesiodistal direction to obtain enamel, dentin, and enamel/dentin samples (2 mm). The fluorescence intensity of specimens was directly measured using an optic fiber associated with a spectrometer (Ocean Optics USB 4000) and recorded in graphic form (Origin 8.0 program). Data were submitted to statistical analysis using Dunnet, Tukey, and Kruskall-Wallis tests. Light absorption of the composite resins was obtained in a spectral range from 250 to 450 nm, and that of dental tissues was between 250 and 300 nm. All composite resins were excited at 398 nm and exhibited maximum emissions of around 485 nm. Fluorescence intensity values for all of the resins showed statistically significant differences (measured in arbitrary units [AUs]), with the exception of groups Z and DVS. Group DVSI had the highest fluorescence intensity values (13539 AU), followed by ODVS (10440 AU), DVS (10146 AU), ES (3946 AU), OES (3841 AU), A (3540 AU), and Z (1146 AU). The fluorescence intensity values for the composite resins differed statistically from those of dental tissues (E=1380 AU; D=6262 AU; E/D=3251 AU). The opacity interfered with fluorescence intensity, and group Z demonstrated fluorescence intensity values closest to that of tooth enamel. It is concluded that the

  17. Microstructures and Grain Refinement of Additive-Manufactured Ti- xW Alloys

    Science.gov (United States)

    Mendoza, Michael Y.; Samimi, Peyman; Brice, David A.; Martin, Brian W.; Rolchigo, Matt R.; LeSar, Richard; Collins, Peter C.

    2017-07-01

    It is necessary to better understand the composition-processing-microstructure relationships that exist for materials produced by additive manufacturing. To this end, Laser Engineered Net Shaping (LENS™), a type of additive manufacturing, was used to produce a compositionally graded titanium binary model alloy system (Ti- xW specimen (0 ≤ x ≤ 30 wt pct), so that relationships could be made between composition, processing, and the prior beta grain size. Importantly, the thermophysical properties of the Ti- xW, specifically its supercooling parameter ( P) and growth restriction factor ( Q), are such that grain refinement is expected and was observed. The systematic, combinatorial study of this binary system provides an opportunity to assess the mechanisms by which grain refinement occurs in Ti-based alloys in general, and for additive manufacturing in particular. The operating mechanisms that govern the relationship between composition and grain size are interpreted using a model originally developed for aluminum and magnesium alloys and subsequently applied for titanium alloys. The prior beta grain factor observed and the interpretations of their correlations indicate that tungsten is a good grain refiner and such models are valid to explain the grain-refinement process. By extension, other binary elements or higher order alloy systems with similar thermophysical properties should exhibit similar grain refinement.

  18. Antimicrobial and mechanical properties of dental resin composite containing bioactive glass.

    Science.gov (United States)

    Korkut, Emre; Torlak, Emrah; Altunsoy, Mustafa

    2016-07-26

    The aim of this study was to evaluate the antimicrobial efficacy and mechanical properties of dental resin composites containing different amounts of microparticulate bioactive glass (BAG). Experimental resin composites were prepared by mixing resin matrix (70% BisGMA and 30% TEGDMA) and inorganic filler with various fractions of BAG to achieve final BAG concentrations of 5, 10 and 30 wt%. Antimicrobial efficacy was assessed in aqueous suspension against Escherichia coli, Staphylococcus aureus and Streptococcus mutans and in biofilm against S. mutans. The effect of incorporation of BAG on the mechanical properties of resin composite was evaluated by measuring the surface roughness, compressive strength and flexural strength. Under the dynamic contact condition, viable counts of E. coli, S. aureus and S. mutans in suspensions were reduced up to 78%, 57% and 50%, respectively, after 90 minutes of exposure to disc-shaped composite specimens, depending on the BAG contents. In 2-day-old S. mutans biofilm, incorporation of BAG into composite at ratios of 10% and 30% resulted in 0.8 and 1.4 log reductions in the viable cell counts compared with the BAG-free composite, respectively. The surface roughness values of composite specimens did not show any significant difference (p>0.05) at any concentration of BAG. However, compressive and flexural strengths of composite were decreased significantly with addition of 30% BAG (p<0.05). The results demonstrated the successful utilization of BAG as a promising biomaterial in resin composites to provide antimicrobial function.

  19. Purification of gamma-amino butyric acid (GABA) from fermentation of defatted rice bran extract by using ion exchange resin

    Science.gov (United States)

    Tuan Nha, Vi; Phung, Le Thi Kim; Dat, Lai Quoc

    2017-09-01

    Rice bran is one of the significant byproducts of rice processing with 10 %w/w of constitution of whole rice grain. It is rich in nutrient compounds, including glutamic acid. Thus, it could be utilized for the fermentation with Lactobateria for synthesis of GABA, a valuable bioactive for antihypertensive effects. However, the concentration and purity of GABA in fermentation broth of defatted rice bran extract is low for production of GABA drug. This research focused on the purification of GABA from the fermentation broth of defatted rice bran extract by using cation exchange resin. The results indicate that, the adsorption isotherm of GABA by Purelite C100 showed the good agreement with Freundlich model, with high adsorption capacity. The effects of pH and concentration of NaCl in eluent on the elution were also investigated. The obtained results show that, at the operating conditions of elution as follows: pH 6.5, 0.8 M of NaCl in eluent, 0.43 of bed volume; concentration of GABA in accumulative eluent, the purity and recovery yield of GABA were 743.8 ppm, 44.0% and 84.2%, respectively. Results imply that, it is feasible to apply cation exchange resin for purification of GABA from fermentation broth of defatted rice bran extract.

  20. Statistical analysis of the equilibrium configurations of the W7-X stellarator using function parameterization

    International Nuclear Information System (INIS)

    Mc Carthy, P.J.; Sengupta, A.; Geiger, J.; Werner, A.

    2005-01-01

    The W7-X stellarator, under construction at IPP-Greifswald, is being designed to demonstrate the steady state capability of fusion devices. Due to the pulse length involved, real time monitoring and control of the discharges is a crucial issue in steady state operations. For W7-X, we have planned a sequence of in-depth analyses of the magnetic configurations which, ultimately, will lead to a proper understanding of plasma equilibrium, stability and transport. It should also provide insight into the parameterization of the various plasma-related quantities which is important from the point of view of real time study. The first step in our sequence of analyses involved a study of the vacuum configuration, including the detectable magnetic islands, of W7-X. We now proceed to the scenario at finite beta considering full magnetohydrodynamic (MHD) equilibria based on vmec2000 calculations. A database of order 10000 equilibria was calculated on the same parameter space for the coil current ratios. The parameters which were varied randomly and independently consist of the external coil current ratios (6), the parameters of the profiles (as functions of normalised toroidal flux) of plasma pressure and toroidal current (4+4) and the plasma size (a eff ) which is required to vary the plasma volume. A statistical analysis, using Function Parametrization (FP), was performed on a sample of well-converged equilibria. The plasma parameters were varied to allow a good FP for the expected values in W7-X, i.e. volume-averaged up to 5% and toroidal net-current of up to ±50 kA for a mean field strength of about 2 T throughout the database. The profiles were chosen as a sequence of polynomials with the property that the addition of a higher order polynomial would not change the lower order volume-averaged moments of the resulting profile. The aim of this was to try to avoid cross correlations in the independent input parameters for the database generation. However, some restrictions