WorldWideScience

Sample records for chemical preparation

  1. Chemical aspects of antiballistic cermets preparation

    Czech Academy of Sciences Publication Activity Database

    Brožek, Vlastimil; Kubatík, Tomáš František; Chráska, Tomáš; Mušálek, Radek; Janata, Marek; Mastný, L.

    Prague: Czech Society of Industrial Chemistry, 2015 - (Kalenda, P.; Lubojacký, J.), s. 218-224. (ICCT). ISBN 978-80-86238-79-1. [International Conference on Chemical Technology-ICCT2015/3./. Mikulov (CZ), 13.04.2015-15.04.2015] R&D Projects: GA MPO FR-TI2/702 Institutional support: RVO:61389021 Keywords : Anti-ballistic ceramics * armour ceramics * plasma spraying * titanium boride * plasma spraying * titanium nitride Subject RIV: CA - Inorganic Chemistry http://www.amca.cz/icct/Full_Papers_ICCT_2015_web.pdf

  2. Chemical flowsheet conditions for preparing urania spheres by internal gelation

    International Nuclear Information System (INIS)

    Small, ceramic urania spheres can be prepared for use as nuclear fuel by internal chemical gelation of uranyl nitrate solution droplets. Decomposition of hexamethylenetetramine (HMTA) dissolved in the uranyl nitrate solution releases ammonia to precipitate hydrated UO3. Previously established flowsheet conditions have been improved and modified at ORNL and have been applied to prepare dense UO2 spheres with average diameters of 1200, 300, and 30 μm

  3. Chemical flowsheet conditions for preparing urania spheres by internal gelation

    International Nuclear Information System (INIS)

    Small, ceramic urania spheres can be prepared for use as nuclear fuel by internal chemical gelation of uranyl nitrate solution droplets. Acid-deficient uranyl nitrate solutions up to 3.4 M in uranium with NO3-U mole ratios of 1.5 to 1.7 are prepared by dissolution of U3O8 or UO3. Decomposition of hexamethylenetetramine dissolved in the uranyl nitrate solution releases ammonia to precipitate hydrated UO/sub 3/. Previously established flowsheet conditions have been improved and modified at ORNL and have been applied to prepare dense UO2 spheres with average diameters of 1200, 300, and 30 μm. The 1200- and 300-μm UO2 spheres were prepared by gelation in trichloroethylene at 50 to 650C; 2-ethyl-1-hexanol was used as the gelation medium to prepare 30-μm UO2 spheres. 8 refs

  4. Exploring Simulator Use in the Preparation of Chemical Engineers

    Science.gov (United States)

    Yerrick, Randy; Lund, Carl; Lee, Yonghee

    2013-01-01

    In this manuscript, we report the impact of students' usage of a simulator in the preparation of chemical engineers. This case study was conducted using content pretest and posttests, survey questionnaires, interviews, classroom observations, and an analysis of students' written response to design problems. Results showed the use of simulator was…

  5. An Overview on Thin Films Prepared by Chemical Vapor Deposition

    International Nuclear Information System (INIS)

    Chemical vapor deposition, (CVD); involves the formation of a solid thin layer on a heated substrate surface by means of chemical reaction in gas or vapor phase. CVD techniques have expanded continuously and developed into the most important method for producing films for solid-state devices. CVD is considered to be the major technique for preparing most films used in the fabrication of semiconductor devices and integrated circuits. It has advantages such as the versatility, compatibility, quality, simplicity, reproducibility, and low cost. CVD has some disadvantages of; the use of comparatively high temperatures in many processes and chemical hazards caused by toxic, explosive, or corrosive gases. Chemical vapor deposition processes can be classified according to the type of their activation energy into thermally-activated CVD, plasma-enhanced CVD, laser-induced CVD, photochemical CVD, and electron-beam assisted CVD. In this paper an attempt is made to present all aspects of CVD equipment design and the variables affecting the deposition rate. Finally the preparation requirements and the application of CVD films are also summarized. 5 figs

  6. Preparation of activated carbon by chemical activation under vacuum.

    Science.gov (United States)

    Juan, Yang; Ke-Qiang, Qiu

    2009-05-01

    Activated carbons especially used for gaseous adsorption were prepared from Chinesefir sawdust by zinc chloride activation under vacuum condition. The micropore structure, adsorption properties, and surface morphology of activated carbons obtained under atmosphere and vacuum were investigated. The prepared activated carbons were characterized by SEM, FTIR, and nitrogen adsorption. It was found that the structure of the starting material is kept after activation. The activated carbon prepared under vacuum exhibited higher values of the BET surface area (up to 1079 m2 g(-1)) and total pore volume (up to 0.5665 cm3 g(-1)) than those of the activated carbon obtained under atmosphere. This was attributed to the effect of vacuum condition that reduces oxygen in the system and limits the secondary reaction of the organic vapor. The prepared activated carbon has well-developed microstructure and high microporosity. According to the data obtained, Chinese fir sawdust is a suitable precursor for activated carbon preparation. The obtained activated carbon could be used as a low-cost adsorbent with favorable surface properties. Compared with the traditional chemical activation, vacuum condition demands less energy consumption, simultaneity, and biomass-oil is collected in the procedure more conveniently. FTIR analysis showed that heat treatment would result in the aromatization of the carbon structure. PMID:19534162

  7. Preparation and physico-chemical evaluation of kshiramandura.

    Science.gov (United States)

    Jadar, P G; Jagadeesh, M S

    2010-04-01

    Mandura (Iron rust) is known by names lohkitta, malayas, ayomala, meaning waste of iron. Among different formulations prescribed for Parinamashoola (Peptic ulcer), in Ayurvedic classics Kshiramandura (Preparation of Iron rust in Milk) is one. Ancient authorities have given similar recipes of Mandura and these medicines are being successfully administered in the management of Peptic ulcer. In Parinamashoola (Peptic ulcer), Acharya Chakradatta mentioned Kshiramandura, as a formulation prepared by taking 384gms of Mandura Bhasma (Incinerated Iron rust), 3 Kg 73 gm of cow's urine and 768gms of cow's milk, boiled and administered in a dose of 500mg. To establish Physical and Chemical factors present in Mandura before and after purification and incineration, the preparation ofKshira mandura was attempted by adopting Quantitative and Qualitative methods. The drugwas identified by the qualities as described in the classics, viz., unctuous, heavy, hard and black in color and absence of hollow space. Mandura was heated in burning charcoal (600-800° c) and dipped in 5 liters of Cow's urine. This process was repeated 7 times, till the Mandura broke. This purified Mandura was then powdered and triturated with decoction ofTerminalia chebula, Terminalia belerica and Emblica officinalis (Triphala kashaya). Thereafter pellets were prepared and dried. The pellets were then sealed in crucibles and heated 30 times in a special type of furnace with temperature of 1000°c (Gajaputa method) to incinerate Mandura and prepare its ash (Bhasma). Cow's urine and milk were added to this Mandura Bhasma and Kshiramandura was prepared. When analyzed it showed 68.3 5% Ferric oxide, 0.66%MgCO(3) and 1.32% CaCO(3). PMID:22557361

  8. Some pitfalls in chemical sample preparation for accelerator mass spectrometry

    International Nuclear Information System (INIS)

    Sophisticated sample preparation including the determination of stable nuclides are an essential prerequisite for high-accuracy accelerator mass spectrometry (AMS) data. Improvements in the low-level regime already paid back, however, some pitfalls still exist or are (re-) appearing due to recent developments: 1.) As most samples prepared for 10Be-AMS need the addition of 9Be in the form of a liquid solution of known 9Be-concentration and commercial solutions contain too much 10Be, solutions from minerals originating from deep mines have been established. Special attention has recently been paid to the preparation of such a 9Be-carrier by the determination of the 9Be-value by an interlaboratory comparison. It could be shown that deviations between different labs exist, thus, it is strongly advised to have such solutions analysed at more than a single lab to prevent incorrect 10Be-results. 2.) In our approach to analyse as many radionuclides as possible in a single meteorite sample, small changes in the established chemical separation have been tested. Though, the secondary formation of partially insoluble compounds of Mg and Al by the pressure digestion is strongly influenced, thus, yielding to too low 27Al-results in the taken aliquot and overall incorrect 26Al-results.

  9. Radiation chemical route for preparation of metal nanoparticles

    International Nuclear Information System (INIS)

    Nanoparticles show properties that are neither seen in the bulk or at atomic level. The unusual properties are governed by quantum size effect. Due to this various methodologies have been endeavored to control the size of the particles. In the present work we show the use of two complimentary techniques (radiation and photo) to synthesize and control the size of the metal particles. In-situ synthesis of fine silver, thallium and cadmium particles has been carried out by gamma-irradiation and electron pulse irradiation at room temperature in the pre-organized gel of polyacrylamide or cyclodextrin cavity. The role of generation of nuclei in high concentrations in stabilization of metal nanoparticles in hydrophobic cavity is shown. Similarly the importance of entrapment of metal ions in the polymer matrix during its formation is highlighted. The work is further extended to exploit the microemulsion droplets for stabilization of Cd nanoparticles. Utility of pulse radiolysis in probing the mechanism of the formation of metal nanoparticles is also shown. Ultrafast laser pulses were employed to control the morphology of the pre-prepared Pt nanoparticles. The changes in reduction of shape and size are considered to occur through melting and vaporization of the nanoparticles. Pt nanoparticles were coated on the inner walls of the tubular pyrex reactor and tested for their catalytic activity for oxidation of CO. It was observed that Pt nanoparticles prepared in the presence of a stabilizer (gelatin) showed a higher tendency to adhere to the inner walls of the pyrex reactor as compared to that prepared in the presence of silica nanoparticles. The catalyst was found to be active at ≥150 degree C giving CO2. Chemically reduced Pt nanoparticles stabilized on silica nanoparticles gave ∼7% CO conversion per hr. However, radiolytically prepared Pt nanoaprticles stabilized by gelatin gave ∼10% conversion per hr. The data indicates that catalytic oxidation of CO takes place by

  10. Surface chemical states of barium zirconate titanate thin films prepared by chemical solution deposition

    International Nuclear Information System (INIS)

    Ba(Zr0.05Ti0.95)O3 (BZT) thin films grown on Pt/Ti/SiO2/Si(1 0 0) substrates were prepared by chemical solution deposition. The structural and surface morphology of BZT thin films has been studied by X-ray diffraction (XRD) and scanning electron microscope (SEM). The results showed that the random oriented BZT thin film grown on Pt/Ti/SiO2/Si(1 0 0) substrate with a perovskite phase. The SEM surface image showed that the BZT thin film was crack-free. And the average grain size and thickness of the BZT film are 35 and 400 nm, respectively. Furthermore, the chemical states and chemical composition of the films were determined by X-ray photoelectron spectroscopy (XPS) near the surface. The XPS results show that Ba, Ti, and Zr exist mainly in the forms of BZT perovskite structure.

  11. Calcium phosphate bioceramics prepared from wet chemically precipitated powders

    Directory of Open Access Journals (Sweden)

    Kristine Salma

    2010-03-01

    Full Text Available In this work calcium phosphates were synthesized by modified wet chemical precipitation route. Contrary to the conventional chemical precipitation route calcium hydroxide was homogenized with planetary mill. Milling calcium oxide and water in planetary ball mill as a first step of synthesis provides a highly dispersed calcium hydroxide suspension. The aim of this work was to study the influence of main processing parameters of wet chemical precipitation synthesis product and to control the morphology, phase and functional group composition and, consequently, thermal stability and microstructure of calcium phosphate bioceramics after thermal treatment. The results showed that it is possible to obtain calcium phosphates with different and reproducible phase compositions after thermal processing (hydroxyapatite [HAp], β-tricalcium phosphate [β-TCP] and HAp/β-TCP by modified wet-chemical precipitation route. The β-TCP phase content in sintered bioceramics samples is found to be highly dependent on the changes in technological parameters and it can be controlled with ending pH, synthesis temperature and thermal treatment. Pure, crystalline and highly thermally stable (up to 1300°C HAp bioceramics with homogenous grainy microstructure, grain size up to 200–250 nm and high open porosity can be successfully obtained by powder synthesized at elevated synthesis temperature of 70°C and stabilizing ending pH at 9.

  12. Preparation of reference materials for frit chemical analysis

    Energy Technology Data Exchange (ETDEWEB)

    Gazulla, M.F.; Gomez, M.P.; Barba, A.; Orduna, M. [Inst. de Tecnologia Ceramica, Univ. Jaume I., Castellon (Spain)

    2002-08-01

    A study was undertaken on how to prepare frit reference materials in which the following elements are analysed: Si, Al, Fe, Ca, Mg, N, K, Ti, Zr, Ba, Pb, Zn, Hf, P, B and Li. The following analytical techniques were used: X-ray fluorescence spectrometry (XRF), inductively coupled plasma optical emission spectrometry (ICP-OES), atomic absorption spectrophotometry (AAS) and titrimetry. Boron and lithium were analysed by ICP-OES, sodium and lithium by AAS, and boron by titrimetry, while the remaining frit elements and sodium were analysed by XRF. The results found by the different methods were compared and each method was validated by means of reference materials. A procedure was established for preparing frit reference materials for calibrating and validating working methods on an industrial scale. (orig.)

  13. Preparation of potassium tantalate thin films through chemical solution deposition

    Czech Academy of Sciences Publication Activity Database

    Buršík, Josef; Drbohlav, Ivo; Vaněk, Přemysl; Železný, Vladimír

    2004-01-01

    Roč. 24, č. 2 (2004), s. 455-462. ISSN 0955-2219 R&D Projects: GA MŠk LN00A028; GA MŠk OC 528.001; GA ČR GA202/02/0238; GA ČR GA202/00/1245 Institutional research plan: CEZ:AV0Z4032918 Keywords : chemical solution deposition * films * tantalates Subject RIV: CA - Inorganic Chemistry Impact factor: 1.483, year: 2004

  14. Oriented Y-typehexagonal ferrite thin films prepared by chemical

    Czech Academy of Sciences Publication Activity Database

    Buršík, Josef; Kužel, R.; Knížek, Karel; Drbohlav, Ivo

    2013-01-01

    Roč. 203, JULY (2013), s. 100-105. ISSN 0022-4596 R&D Projects: GA ČR GA13-03708S Institutional support: RVO:61388980 ; RVO:68378271 Keywords : Y-type hexagonal ferrites * chemical solution deposition * thin films * epitaxial growth Subject RIV: CA - Inorganic Chemistry; BM - Solid Matter Physics ; Magnetism (FZU-D) Impact factor: 2.200, year: 2013

  15. High index of refraction films for dielectric mirrors prepared by metal-organic chemical vapor deposition

    International Nuclear Information System (INIS)

    A wide variety of metal oxides with high index of refraction can be prepared by Metal-Organic Chemical Vapor Deposition. We present some recent optical and laser damage results on oxide films prepared by MOCVD which could be used in a multilayer structure for highly reflecting (HR) dielectric mirror applications. The method of preparation affects both optical properties and laser damage threshold. 10 refs., 8 figs., 4 tabs

  16. Bhasmas: unique ayurvedic metallic-herbal preparations, chemical characterization.

    Science.gov (United States)

    Kumar, A; Nair, A G C; Reddy, A V R; Garg, A N

    2006-03-01

    Bhasmas are unique Ayurvedic metallic preparations with herbal juices/fruits, known in the Indian subcontinent since the seventh century BC and widely recommended for treatment of a variety of chronic ailments. Twenty bhasmas based on calcium, iron, zinc, mercury, silver, potassium, arsenic, copper, tin, and gemstones were analyzed for up to 18 elements by instrumental neutron activation analysis, including their C, H, N, and S contents. In addition to the major constituent element found at % level, several other essential elements such as Na, K, Ca, Mg, V, Mn, Fe, Cu, and Zn have also been found in microg/g amounts and ultratrace (ng/g) amounts of Au and Co. These seem to remain chelated with organic ligands derived from medicinal herbs. The bhasmas are biologically produced nanoparticles and are taken along with milk, butter, honey, or ghee (a preparation from milk); thus, this makes these elements easily assimilable, eliminating their harmful effects and enhancing their biocompatibility. Siddha Makaradhwaja, a mercury preparation is found to be stoichiometrically HgS without any traces of any other element. Similarly, Swet Parpati is stoichiometrically KNO3 but is found to have Mn, Cu, Zn, Na, P, and Cl as well. An attempt has been made to correlate the metallic contents with their medicinal importance. Na and K, the two electrolytic elements, seem to be well correlated, although K/Na varies in a wide range from 0.06 to 95, with specifically low values for Ca-, Fe-, and Zn-based bhasmas. K/P also varies in a wide range from 0.23 to 12, although for most bhasmas (n = 12), it is 2.3 +/- 1.2. Further, Fe/Mn is linearly correlated (r = 0.96) with Fe in nine noniron bhasmas. PMID:16632893

  17. Influence of particle size and preparation methods on the physical and chemical stability of amorphous simvastatin

    DEFF Research Database (Denmark)

    Zhang, Fang; Aaltonen, Jaakko; Tian, Fang;

    2009-01-01

    using DSC in order to link the physical and chemical stability with molecular mobility. Chemical stability was studied with high-performance liquid chromatography (HPLC). Results obtained from the current study revealed that the solubility of amorphous forms prepared by both methods was enhanced...

  18. Chemically durable phosphate glasses and a method for their preparation

    Science.gov (United States)

    Day, D.E.; Wilder, J.A. Jr.

    The chemical durability of alkali phosphate glasses is improved by incorporation of up to 23 weight percent of nitrogen. A typical phosphate glass contains: 10 to 60 mole % of Li/sub 2/O, Na/sub 2/O or K/sub 2/O; 5 to 40 mole % of BaO or CaO; 0 to 1 to 10 mole % of Al/sub 2/O/sub 3/; and 40 to 70 mole % of P/sub 2/O/sub 5/. Nitrides, such as AlN, are the favored additives.

  19. Preparation and characterization of a chemically sulfated cashew gum polysaccharide

    Energy Technology Data Exchange (ETDEWEB)

    Moura Neto, Erico de; Maciel, Jeanny da S.; Cunha, Pablyana L. R.; Paula, Regina Celia M. de; Feitosa, Judith P.A., E-mail: judith@dqoi.ufc.br [Departamento de Quimica Organica e Inorganica, Universidade Federal do Ceara, Fortaleza (Brazil)

    2011-09-15

    Cashew gum (CG) was sulfated in pyridine:formamide using chlorosulfonic acid as the reagent. Confirmation of sulfation was obtained by Fourier transform infrared (FTIR) spectroscopy through the presence of an asymmetrical S=O stretching vibration at 1259 cm{sup -1}. The degrees of substitution were 0.02, 0.24 and 0.88 determined from the sulfur percentage. 1D and 2D nuclear magnetic resonance (NMR) data showed that the sulfation occurred at primary carbons. An increase of at least 4% of the solution viscosity was observed due to sulfation. The thermal gravimetric curves (TGA) indicate that the derivatives are stable up to ca. 200 deg C. The sulfated CG is compared to carboxymethylated CG in order to verify the possibility of the use of the former in the preparation of polyelectrolyte complexes; the latter is already being used for this application. (author)

  20. Sediment losses from forest management: mechanical vs. chemical site preparation after clearcutting

    Energy Technology Data Exchange (ETDEWEB)

    Beasley, R.S.; Granillo, A.B.; Zillmer, V.

    The comparative effects of mechanical and chemical site preparation water yields and sediment losses following forest clearcutting were evaluated over a 4-yr period in the Athens Plateau area of southwestern Arkansas. After 1 yr of pretreatment measurements, three forested water sheds were clearcut and the residual vegetation and debris were sheared and windrowed but not burned. Three watersheds were clearcut in a similar manner, but received chemical site preparation. Residual trees on two watersheds were injected with 2-4, D amine; the third watershed was aerially sprayed with a mixture of Tordon (active ingredient: picloram (4-amino-3,5,6-trichloropicoline acid)) and Garlon (active ingredient; triclopyr (3,5,6-trichloro-2-pyridinyloxyacetic acid)). Three additional watersheds were left undisturbed for controls. Mean annual sediment losses on the mechanically, site prepared watersheds during the first posttreatment year were significantly higher than those from either the chemically site prepared watersheds or controls. Chemical site preparation did not significantly increase sediment losses. Although 2nd yr losses for the mechanical site preparation and control treatments doubled over 1st-yr levels, no significant treatment effect was detected for either site preparation treatment. Third-year losses decreased below 1st-yr losses for all treatments but not to pretreatment year levels. The relatively sharp declines in sediment losses during the third posttreatment year were attributed to rapid regrowth of natural vegetation on the sites.

  1. Chemical and electrical properties of LSM cathodes prepared by mechanosynthesis

    Science.gov (United States)

    Moriche, R.; Marrero-López, D.; Gotor, F. J.; Sayagués, M. J.

    2014-04-01

    Mechanosynthesis of La1-xSrxMnO3 (x = 0, 0.25, 0.5, 0.75 and 1) was carried out at room temperature from stoichiometric mixtures of La2O3, Mn2O3 and SrO, obtaining monophasic powders with the perovskite structure. Physical properties of these materials and their chemical compatibility with the electrolyte yttria stabilized zirconia (YSZ), which depend strongly on the La/Sr ratio, were evaluated to corroborate availability to be implemented as cathode material in solid oxide fuel cells (SOFCs). Electrical conductivity values in air ranged between 100 and 400 S cm-1 in the temperature range of 25-850 °C. Samples presented low reactivity with YSZ in the working temperature range (600-1000 °C) maintaining the grain size small enough to preserve the catalytic activity for oxygen reduction.

  2. La-Zn Substituted Hexaferrites Prepared by Chemical Method

    International Nuclear Information System (INIS)

    La-Zn substituted M-type Ba hexaferrite powders were prepared by sol-gel (Mx) and organometallic precursor (Sk) methods with Fe/Ba ratio of 11.6 and 10.8, respectively. The compositions (LaZn)xBa1-xFe12-xO19 with 0.0 ≤ x ≤ 0.6 were annealed at 975oC/2 h. The cationic site preferences of nonmagnetic La3+ instead of Ba2+ ions and Zn2+ instead of Fe3+ ions were determined by Moessbauer spectroscopy. The La3+ ions substitute the large Ba2+ ions at 2a site and for x ≥ 0.4 also at 4f2 site. The nearly all Zn2+ ions are placed at the 4f1 sites. The thermomagnetic analysis of χ(θ) confirms that only the small substitutions for x ≤ 0.4 can be taken as a single-phase hexaferrites. The coercivity Hc almost does not change at x = 0.2 for (Mx) samples and further decrease up to x = 0.6. For (Sk) samples at substitution x = 0.2 the values of Hc are decreasing and at higher x the values nearly do not change. The Curie points, Tc, slowly decrease with x for both (Mx) and (Sk) samples.

  3. Textural and chemical properties of zinc chloride activated carbons prepared from pistachio-nut shells

    International Nuclear Information System (INIS)

    The effects of activation temperature on the textural and chemical properties of the activated carbons prepared from pistachio-nut shells using zinc chloride activation under both inert nitrogen gas atmosphere and vacuum condition were studied. Relatively low temperature of 400 deg. C was beneficial for the development of pore structures. Too high an activation temperature would lead to sintering of volatiles and shrinkage of the carbon structure. The microstructures and microcrystallinity of the activated carbons prepared were examined by scanning electron microscope and powder X-ray diffraction techniques, respectively, while Fourier transform infrared spectra determined the changes in the surface functional groups at the various stages of preparation

  4. Amorphous TM1−xBx alloy particles prepared by chemical reduction (invited)

    DEFF Research Database (Denmark)

    Linderoth, Søren; Mørup, Steen

    1991-01-01

    Amorphous transition-metal boron (TM-B) alloy particles can be prepared by chemical reduction of TM ions by borohydride in aqueous solutions. ln the last few years systematic studies of the parameters which control the composition, and, in turn, many of the properties of the alloy particles, have...... been performed and are reviewed in the present paper. The most important preparation parameters which influence the composition are the concentration of the borohydride solution and the pH of the TM salt solution. By controlling these parameters it is possible to prepare amorphous alloy samples...

  5. Preparation Of Polystyrene Nanoparticles Using Both GAMMA Radiation And Chemical Induced Emulsion Polymerization

    International Nuclear Information System (INIS)

    Polystyrene nanoparticles were synthesized by radiation-induced polymerization and chemical emulsion polymerization. Compared with the chemical emulsion polymerization, the radiation process easily prepared the polystyrene (PS) nanoparticles at room temperature and without the pollutant of chemical initiator. The effects of various polymerization parameters in both systems such as total dose for radiation polymerization, monomer concentration, sodium dodecyl sulfate (SDS) stabilizer content on the particle size and size distribution were systematically investigated. The diameter of a polymer particle and its distribution were measured on a Marvern Zetasizer. Monomer conversion was studied gravimetric ally and the structure of PS was analyzed by Differential Scanning Calorimeter (DSC) and Fourier Transform Infrared (FT-IR) Spectrophotometer

  6. Preparation and characterization of ZnS thin films by the chemical bath deposition method

    Energy Technology Data Exchange (ETDEWEB)

    Iwashita, Taisuke [Department of Electrical Engineering, Faculty of Engineering, Tokyo University of Science 1-14-6 Kudankita, Chiyoda, Tokyo 102-0073 (Japan); Ando, Shizutoshi, E-mail: ando_shi@rs.kagu.tus.ac.jp [Department of Electrical Engineering, Faculty of Engineering, Tokyo University of Science 1-14-6 Kudankita, Chiyoda, Tokyo 102-0073 (Japan); Research Institute for Science and Technology, Advanced Device Laboratories (ADL), Tokyo University of Science, 1-3 Kagurazaka, Shinjuku, Tokyo 162-8601 (Japan); Research Institute for Science and Technology, Photovoltaic Science and Technology Research Division, Tokyo University of Science, 1-3 Kagurazaka, Shinjuku, Tokyo 162-8601 (Japan)

    2012-10-01

    ZnS thin films prepared on quartz substrates by the chemical bath deposition (CBD) method with three type temperature profile processes have been investigated by X-ray diffraction, scanning electron microscope, energy dispersive X-ray analysis and light transmission. One is a 1-step growth process, and the other is 2-steps growth and self-catalyst growth processes. The surface morphology of CBD-ZnS thin films prepared by the CBD method with the self-catalyst growth process is flat and smooth compared with that prepared by the 1-step and 2-steps growth processes. The self-catalyst growth process in order to prepare the particles of ZnS as initial nucleus layer was useful for improvement in crystallinity of ZnS thin films prepared by CBD. ZnS thin films prepared by CBD method with self-catalyst growth process can be expected for improvement in the conversion efficiency of Cu(InGa)Se{sub 2}-based thin film solar cells by using it for the buffer layer. - Highlights: Black-Right-Pointing-Pointer ZnS thin films were prepared by chemical bath deposition (CBD) method. Black-Right-Pointing-Pointer The crystallization of CBD-ZnS films was further improved. Black-Right-Pointing-Pointer The crystallinity of CBD-ZnS thin films is dependent on the zinc source material. Black-Right-Pointing-Pointer Self-catalyst growth process is useful for the growth of thin films by CBD method. Black-Right-Pointing-Pointer It is expected to improve the conversion efficiency of CuIn{sub 1-x}Ga{sub x}Se{sub 2} solar cells.

  7. XRD and UV-vis results of Tungstein oxide thin films prepared by chemical bath deposition

    International Nuclear Information System (INIS)

    In the experiment, using a simple, economical, chemical bath method for depositing tungstein oxide films, electrochromic tungstein oxide thin films were prepared from an aqueous solution of Na2WO4H2O and diethyl sulfate at boiling temperature on ITO coated glass substrate. The techniques such as X-ray and UV-VIS-spectroscopy diffraction were used for the characterization of the films. According to the results of X-ray and UV-VIS, WOx thin film is very promising material for electrochromic applications and this is simply and economically produced by chemical bath method

  8. Preparing Federal Coordinating Officers (FCOs) to operate in Chemical, Biological, Radiological, and Nuclear (CBRN) environments

    OpenAIRE

    Russell, Tony.

    2008-01-01

    CHDS State/Local In this thesis the Federal Emergency Management Agency's (FEMA) Federal Coordinating Officer (FCO) function is examined as it relates to Chemical, Biological, Radiological and Nuclear (CBRN) operations. It is suggested that targeted changes can be made to ensure the FCOs are better prepared to manage the additional complexities of a CBRN environment. The changes include addressing the FCOs from the systems approach- internally to improve the FCO personal and professio...

  9. Preparation and Characterization of Chitosan/Agar Blended Films: Part 1. Chemical Structure and Morphology

    OpenAIRE

    Esam A. El-Hefian; Mohamed Mahmoud NASEF; Yahaya, Abdul Hamid

    2012-01-01

    Chitosan/agar (CS/AG) films were prepared by blending different proportions of chitosan and agar (considering chitosan as the main component) in solution forms. The chemical structure and the morphology of the obtained blended films were investigated using Fourier transform infrared (FTIR) and field emission scanning electron microscope (FESEM). It was revealed that chitosan and agar form a highly compatible blend and their films displayed homogenous and smooth surface properties compared to ...

  10. Polyoxometalate based soft chemical route for preparation of Pt nanorods and self-assemblies

    Indian Academy of Sciences (India)

    S Shanmugam; B Viswanathan; T K Varadarajan

    2005-10-01

    A soft chemical route is described for the preparation of platinum nanorods and self-assemblies over photochemically reduced polyoxometalate (silicotungstate) containing composite films. Transmission electron microscopy shows that the diameters of the platinum nanorods are around 55–60 nm. The formation of platinum nanorods on solid–liquid interface reactions was explained on the basis of single site growth mechanism and diffusion limitation aggregation process.

  11. Preparation and thermal conductivity of CuO nanofluid via a wet chemical method

    OpenAIRE

    Zhu Haitao; Han Dongxiao; Meng Zhaoguo; Wu Daxiong; Zhang Canying

    2011-01-01

    Abstract In this article, a wet chemical method was developed to prepare stable CuO nanofluids. The influences of synthesis parameters, such as kinds and amounts of copper salts, reaction time, were studied. The thermal conductivities of CuO nanofluids were also investigated. The results showed that different copper salts resulted in different particle morphology. The concentration of copper acetate and reaction time affected the size and shape of clusters of primary nanoparticles. Nanofluids...

  12. The Electrochemical Characteristics of Hybrid Capacitor Prepared by Chemical Activation of NaOH

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Jeong Eun; Bae, Ga Yeong; Yang, Jeong Min; Lee, Jong Dae [Chungbuk National Univ., Chungju (Korea, Republic of)

    2013-06-15

    Active carbons with high specific surface area and micro pore structure were prepared from the coconut shell char using the chemical activation method of NaOH. The preparation process has been optimized through the analysis of experimental variables such as activating chemical agents to char ratio and the flow rate of gas during carbonization. The active carbons with the surface area (2,481m{sup 2}/g) and mean pore size (2.32 nm) were obtained by chemical activation with NaOH. The electrochemical performances of hybrid capacitor were investigated using LiMn{sub 2}O{sub 4}, LiCoO{sub 2} as the positive electrode and prepared active carbon as the negative electrode. The electrochemical behaviors of hybrid capacitor using organic electrolytes (LiPF{sub 6}, TEABF{sub 4}) were characterized by constant current charge/discharge, cyclic voltammetry, cycle and leakage tests. The hybrid capacitor using LiMn{sub 2}O{sub 4}/AC electrodes had better capacitance than other hybrid systems and was able to deliver a specific energy as high as 131 Wh/kg at a specific power of 1,448 W/kg.

  13. Preparation and Characterization of Sisal Fiber-based Activated Carbon by Chemical Activation with Zinc Chloride

    International Nuclear Information System (INIS)

    Sisal fiber, an agricultural resource abundantly available in China, has been used as raw material to prepare activated carbon with high surface area and huge pore volume by chemical activation with zinc chloride. The orthogonal test was designed to investigate the influence of zinc chloride concentration, impregnation ratio, activation temperature and activation time on preparation of activated carbon. Scanning electron micrograph, Thermo-gravimetric, N2-adsorption isotherm, mathematical models such as t-plot, H-K equation, D-R equation and BJH methods were used to characterize the properties of the prepared carbons and the activation mechanism was discussed. The results showed that ZnCl2 changed the pyrolysis process of sisal fiber. Characteristics of activated carbon are: BET surface area was 1628 m2/g, total pore volume was 1.316 m3/g and ratio of mesopore volume to total pore volume up to 94.3%. These results suggest that sisal fiber is an attractive source to prepare mesoporous high-capacity activated carbon by chemical activation with zinc chloride

  14. Electroluminescence and photoluminescence of conjugated polymer films prepared by plasma enhanced chemical vapor deposition of naphthalene

    CERN Document Server

    Rajabi, Mojtaaba; Firouzjah, Marzieh Abbasi; Hosseini, Seyed Iman; Shokri, Babak

    2012-01-01

    Polymer light-emitting devices were fabricated utilizing plasma polymerized thin films as emissive layers. These conjugated polymer films were prepared by RF Plasma Enhanced Chemical Vapor Deposition (PECVD) using naphthalene as monomer. The effect of different applied powers on the chemical structure and optical properties of the conjugated polymers was investigated. The fabricated devices with structure of ITO/PEDOT:PSS/ plasma polymerized Naphthalene/Alq3/Al showed broadband Electroluminescence (EL) emission peaks with center at 535-550 nm. Using different structural and optical tests, connection between polymers chemical structure and optical properties under different plasma powers has been studied. Fourier transform infrared (FTIR) and Raman spectroscopies confirmed that a conjugated polymer film with a 3-D cross-linked network was developed. By increasing the power, products tended to form as highly cross-linked polymer films. Photoluminescence (PL) spectra of plasma polymers showed different excimerc ...

  15. Chemical Properties of Carbon Nanotubes Prepared Using Camphoric Carbon by Thermal-CVD

    International Nuclear Information System (INIS)

    Chemical properties and surface study on the influence of starting carbon materials by using thermal chemical vapor deposition (Thermal-CVD) to produced carbon nanotubes (CNTs) is investigated. The CNTs derived from camphor were synthesized as the precursor material due to low sublimation temperature. The major parameters are also evaluated in order to obtain high-yield and high-quality CNTs. The prepared CNTs are examined using field emission scanning electron microscopy (FESEM) to determine the microstructure of nanocarbons. The FESEM investigation of the CNTs formed on the support catalysts provides evidence that camphor is suitable as a precursor material for nanotubes formation. The chemical properties of the CNTs were conducted using FTIR spectroscopy and PXRD analysis. The high-temperature graphitization process induced by the Thermal-CVD enables the hydrocarbons to act as carbon sources and changes the aromatic species into the layered graphite structure of CNTs.

  16. Research and Development Aspects on Chemical Preparation Techniques of Photoanodes for Dye Sensitized Solar Cells

    Directory of Open Access Journals (Sweden)

    Nilofar Asim

    2014-01-01

    Full Text Available The importance of dye sensitized solar cells (DSSCs as a low-cost and environmentally friendly photovoltaic (PV technology has prompted many researchers to improve its efficiency and durability. The realization of these goals is impossible without taking into account the importance of the materials in DSSCs, so the focus on the preparation/deposition methods is essential. These methods can be either chemical or physical. In this study, the chemical applied methods that utilize chemical reaction to synthesize and deposit the materials are covered and categorized according to their gas phase and liquid phase precursors. Film processing techniques that can be used to enhance the materials' properties postpreparation are also included for further evaluation in this study. However, there is a variety of consideration, and certain criteria must be taken into account when selecting a specific deposition method, due to the fact that the fabrication conditions vary and are unoptimized.

  17. Chemical Properties of Carbon Nanotubes Prepared Using Camphoric Carbon by Thermal-CVD

    Science.gov (United States)

    Azira, A. A.; Rusop, M.

    2010-03-01

    Chemical properties and surface study on the influence of starting carbon materials by using thermal chemical vapor deposition (Thermal-CVD) to produced carbon nanotubes (CNTs) is investigated. The CNTs derived from camphor were synthesized as the precursor material due to low sublimation temperature. The major parameters are also evaluated in order to obtain high-yield and high-quality CNTs. The prepared CNTs are examined using field emission scanning electron microscopy (FESEM) to determine the microstructure of nanocarbons. The FESEM investigation of the CNTs formed on the support catalysts provides evidence that camphor is suitable as a precursor material for nanotubes formation. The chemical properties of the CNTs were conducted using FTIR spectroscopy and PXRD analysis. The high-temperature graphitization process induced by the Thermal-CVD enables the hydrocarbons to act as carbon sources and changes the aromatic species into the layered graphite structure of CNTs.

  18. Characterization and photo-chemical applications of nano-ZnO prepared by wet chemical and thermal decomposition methods

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • Nano-ZnO particles were synthesized by soft-wet precipitation and dry methods. • ZnO nanoparticle with different morphologies was obtained. • Nano ZnO samples showed a high photocatalytic activity. • ZnO nanoparticle showed strong ultraviolet emission at room temperature. • The samples showed high biological activity depending on their synthetic method. - Abstract: Nano-crystalline ZnO particles were synthesized using two different routes: soft-wet and dry methods. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were used to identify the particles structures and morphologies, while X-ray diffraction (XRD) was used for verifying the particles crystal structure. The thermal stabilities of the particles were examined through thermal gravimetric analysis technique and their surface areas were calculated using BET method. Moreover, the photocatalytic activities were evaluated using UV–vis spectroscopy and photoluminescence (PL) characterization. The results showed that all the prepared ZnO samples possess a hexagonal wurtzite structure with high purity. Different particle sizes and morphologies of spheres, rods and wires were obtained depending on the preparation method used. Particle sizes obtained by the dry method are smaller than that found by the wet chemical method. The effects of both particle size and morphology on each of surface as well as optical properties, photocatalytic activity, dye/ZnO solar cell efficiency and biological activity have been studied and discussed

  19. Dielectric behaviour of MgFe2O4 prepared from chemically beneficiated iron ore rejects

    Indian Academy of Sciences (India)

    K S Rane; V M S Verenkar; P Y Sawant

    2001-06-01

    Chemically beneficiated high silica/alumina iron ore rejects (27–76% Fe2O3) were used to synthesize iron oxides of purity 96–98% with SiO2/Al2O3 ratio reduced to 0.03. The major impurities on chemical beneficiations were Al, Si, and Mn in the range 2–3%. A 99.73% purity Fe2O3 was also prepared by solvent extraction method using methyl isobutyl ketone (MIBK) from the acid extracts of the ore rejects. The magnesium ferrite, MgFe2O4, prepared from these synthetic iron oxides showed high resistivity of ∼ 108 ohm cm. All ferrites showed saturation magnetization, 4s, in the narrow range of 900–1200 Gauss and the Curie temperature, c, of all these fell within a small limit of 670 ± 30 K. All ferrites had low dielectric constants ('), 12–15, and low dielectric loss, tan , which decreased with the increase in frequency indicating a normal dielectric dispersion found in ferrites. The presence of insignificant amount of polarizable Fe2+ ions can be attributed to their high resistances and low dielectric constants. Impurities inherent in the samples had no marked influence on the electrical properties of the ferrites prepared from the iron ore rejects, suggesting the possibility of formation of ferrite of constant composition, MgFe2O4, of low magnetic and dielectric losses at lower temperatures of 1000°C by ceramic technique.

  20. Tracing origins of complex pharmaceutical preparations using surface desorption atmospheric pressure chemical ionization mass spectrometry.

    Science.gov (United States)

    Zhang, Xinglei; Jia, Bin; Huang, Keke; Hu, Bin; Chen, Rong; Chen, Huanwen

    2010-10-01

    A novel strategy to trace the origins of commercial pharmaceutical products has been developed based on the direct chemical profiling of the pharmaceutical products by surface desorption atmospheric pressure chemical ionization mass spectrometry (DAPCI-MS). Besides the unambiguous identification of active drug components, various compounds present in the matrixes are simultaneously detected without sample pretreatment, providing valuable information for drug quality control and origin differentiation. Four sources of commercial amoxicillin products made by different manufacturers have been successfully differentiated. This strategy has been extended to secerning six sources of Liuwei Dihuang Teapills, which are herbal medicine preparations with extremely complex matrixes. The photolysis status of chemical drug products and the inferior natural herd medicine products prepared with different processes (e.g., extra heating) were also screened using the method reported here. The limit of detection achieved in the MS/MS experiments was estimated to be 1 ng/g for amoxicillin inside the capsule product. Our experimental data demonstrate that DAPCI-MS is a useful tool for rapid pharmaceutical analysis, showing promising perspectives for tracking the entire pharmaceutical supply chain to prevent counterfeit intrusions. PMID:20809628

  1. Microwave absorbing properties and enhanced infrared reflectance of Fe/Cu composites prepared by chemical plating

    International Nuclear Information System (INIS)

    Fe/Cu composite samples with Cu particles depositing on carbonyl iron sheets were prepared by chemical plating. Cu additions were uniformly distributed on the grain boundaries of the flaky carbonyl iron while keeping the internal structure of iron. Meanwhile, we found that the chemical plating time made a key point on both the microwave absorbing properties and infrared emissivity. With the growth of chemical plating time, the value of reflection loss gives a linear decrease and the infrared emissivity is reduced with a tendency of index reduction. When the plating time is less than 30 min, the reflection loss of the samples maintains above −20 GHz, moreover, prolonging the plating time more than 30 min, the infrared emissivity of the samples is reduced to 0.50 or less. It can be concluded that both the microwave absorbing and infrared properties are excellent at the optimal plating time of 30 min. - Highlights: • The Fe/Cu composites have been prepared by flake carbonyl iron as substrate. • The Fe/Cu composites exhibit enhanced Infrared characteristics. • The samples hold the most of the absorbing capacity and possess low infrared emissivity by controlling plating time

  2. Characteristics of Barium Hexaferrite Nanoparticles Prepared by Temperature-Controlled Chemical Coprecipitation

    International Nuclear Information System (INIS)

    Ba-ferrite (BaFe12O19) nanoparticles were synthesized by chemical coprecipitation method in an aqueous solution. The particle size and the crystallization temperature of the Ba-ferrite nanoparticles were controlled varying the precipitation temperature. The precipitate that was prepared at 0 .deg. C showed the crystal structure of Ba-ferrite in X-ray diffraction when it was calcined at the temperature above 580 .deg. C, whereas what was prepared at 50 .deg. C showed the crystallinity when it was calcined at the temperature higher than about 700 .deg. C. The particle sizes of the synthesized Ba-ferrite were in a range of about 20-30 nm when it was prepared by being precipitated at 0 .deg. C and calcined at 650 .deg. C. When the precipitation temperature increased, the particle size also increased even at the same calcination temperature. The magnetic properties of the Ba-ferrite nanoparticles were also controlled by the synthetic condition of precipitation and calcination temperature. The coercive force could be appreciably lowered without a loss of saturation magnetization when the Ba-ferrite nanoparticles were prepared by precipitation and calcination both at low temperatures

  3. Characteristics of Barium Hexaferrite Nanoparticles Prepared by Temperature-Controlled Chemical Coprecipitation

    Energy Technology Data Exchange (ETDEWEB)

    Kwak, Jun Young; Lee, Choong Sub; Kim, Don; Kim, Yeong Il [Pukyong National Univ., Busan (Korea, Republic of)

    2012-10-15

    Ba-ferrite (BaFe{sub 12}O{sub 19}) nanoparticles were synthesized by chemical coprecipitation method in an aqueous solution. The particle size and the crystallization temperature of the Ba-ferrite nanoparticles were controlled varying the precipitation temperature. The precipitate that was prepared at 0 .deg. C showed the crystal structure of Ba-ferrite in X-ray diffraction when it was calcined at the temperature above 580 .deg. C, whereas what was prepared at 50 .deg. C showed the crystallinity when it was calcined at the temperature higher than about 700 .deg. C. The particle sizes of the synthesized Ba-ferrite were in a range of about 20-30 nm when it was prepared by being precipitated at 0 .deg. C and calcined at 650 .deg. C. When the precipitation temperature increased, the particle size also increased even at the same calcination temperature. The magnetic properties of the Ba-ferrite nanoparticles were also controlled by the synthetic condition of precipitation and calcination temperature. The coercive force could be appreciably lowered without a loss of saturation magnetization when the Ba-ferrite nanoparticles were prepared by precipitation and calcination both at low temperatures.

  4. Preparation and characterization of nanostructured copper bismuth diselenide thin films from a chemical route

    Indian Academy of Sciences (India)

    R H Bari; L A Patil

    2010-12-01

    Thin films of copper bismuth diselenide were prepared by chemical bath deposition technique onto glass substrate below 60°C. The deposition parameters such as time, temperature of deposition and pH of the solution, were optimized. The set of films having different elemental compositions was prepared by varying Cu/Bi ratio from 0.13–1.74. Studies on structure, composition, morphology, optical absorption and electrical conductivity of the films were carried out and discussed. Characterization includes X-ray diffraction (XRD), scanning electron microscopy (SEM), atomic force microscopy (AFM), energy dispersive X-ray analysis (EDAX), absorption spectroscopy, and electrical conductivity. The results are discussed and interpreted.

  5. Thermoelectric Power of Nanocrystalline Silicon Prepared by Hot-Wire Chemical-Vapor Deposition

    Science.gov (United States)

    Kearney, Brian; Liu, Xiao; Jugdersuren, Battogtokh; Queen, Daniel; Metcalf, Thomas; Culbertson, James; Chervin, Christopher; Stroud, Rhonda; Nemeth, William; Wang, Qi

    Although doped bulk silicon possesses a favorable Seebeck coefficient and electrical conductivity, its thermal conductivity is too large for practical thermoelectric applications. Thin film nanocrystalline silicon prepared by hot-wire chemical-vapor deposition (HWCVD) is an established material used in multijunction amorphous silicon solar cells. Its potential in low cost and scalable thermoelectric applications depends on achieving a low thermal conductivity without sacrificing thermoelectric power and electrical conductivity. We examine the thermoelectric power of boron-doped HWCVD nanocrystalline silicon and find that it is comparable to doped nanostructured silicon alloys prepared by other methods. Given the low thermal conductivity and high electrical conductivity of these materials, they can achieve a high thermoelectric figure of merit, ZT. Work supported by the Office of Naval Research.

  6. Studies on transparent spinel magnesium indium oxide thin films prepared by chemical spray pyrolysis

    International Nuclear Information System (INIS)

    Ternary semiconducting oxide compound magnesium indium oxide films (MgIn2O4), manifesting high transparency were prepared by metal organic chemical spray pyrolysis technique. Precursors prepared for various cationic ratios of Mg/In = 0.35, 0.40, 0.45 and 0.50 were thermally sprayed onto quartz substrates, decomposed at 450 deg. C and the spinel phase evolution was studied. X-ray diffraction, Rutherford backscattering and X-ray photoelectron spectroscopy studies have been conducted to confirm the formation of single-phase MgIn2O4 films with Mg/In ratio 0.50. From optical transmission studies, the observed optical band gaps varied from 3.18 to 3.86 eV (0.35 -5 S cm-1) and the Hall coefficient showed n-type electrical conduction and high carrier concentration (0.16 x 1020-0.89 x 17 cm-3)

  7. Near net shape forming processes for chemically prepared zinc oxide varistors.

    Energy Technology Data Exchange (ETDEWEB)

    Lockwood, Steven John; Voigt, James A.; Tuttle, Bruce Andrew; Bell, Nelson Simmons

    2005-01-01

    Chemically prepared zinc oxide powders are fabricated for the production of high aspect ratio varistor components. Colloidal processing in water was performed to reduce agglomerates to primary particles, form a high solids loading slurry, and prevent dopant migration. The milled and dispersed powder exhibited a viscoelastic to elastic behavioral transition at a volume loading of 43-46%. The origin of this transition was studied using acoustic spectroscopy, zeta potential measurements and oscillatory rheology. The phenomenon occurs due to a volume fraction solids dependent reduction in the zeta potential of the solid phase. It is postulated to result from divalent ion binding within the polyelectrolyte dispersant chain, and was mitigated using a polyethylene glycol plasticizing additive. Chemically prepared zinc oxide powders were processed for the production of high aspect ratio varistor components. Near net shape casting methods including slip casting and agarose gelcasting were evaluated for effectiveness in achieving a uniform green microstructure achieving density values near the theoretical maximum during sintering. The structure of the green parts was examined by mercury porisimetry. Agarose gelcasting produced green parts with low solids loading values and did not achieve high fired density. Isopressing the agarose cast parts after drying raised the fired density to greater than 95%, but the parts exhibited catastrophic shorting during electrical testing. Slip casting produced high green density parts, which exhibited high fired density values. The electrical characteristics of slip cast parts are comparable with dry pressed powder compacts. Alternative methods for near net shape forming of ceramic dispersions were investigated for use with the chemically prepared ZnO material. Recommendations for further investigation to achieve a viable production process are presented.

  8. Characterization and Functional Applications of Nanoporous Ag Foams Prepared by Chemical Dealloying

    Science.gov (United States)

    Wu, T. Y.; Wang, X.; Huang, J. C.; Tsai, W. Y.; Chu, Y. Y.; Chen, S. Y.; Du, X. H.

    2015-10-01

    In this study, the pure Ag nanoporous foams, with open cell pore volume fractions 55 to 70 pct and pore sizes 100 to 400 nm, have been prepared by chemical dealloying. The Ag nanoporous foams possess favorable modulus (~0.7 GPa) and strength (~14 MPa), much higher than most of the polymers or ceramic foams. It is found that the Ag nanoporous foams are appropriate candidates for the catalytic and electrode applications. However, they do not exhibit efficient anti-bacterial effect, unless much smaller bacteria with cell sizes of 100 nm or less in the neighborhood are encountered.

  9. High quality thin films of thermoelectric misfit cobalt oxides prepared by a chemical solution method

    Science.gov (United States)

    Rivas-Murias, Beatriz; Manuel Vila-Fungueiriño, José; Rivadulla, Francisco

    2015-07-01

    Misfit cobaltates ([Bi/Ba/Sr/Ca/CoO]nRS[CoO2]q) constitute the most promising family of thermoelectric oxides for high temperature energy harvesting. However, their complex structure and chemical composition makes extremely challenging their deposition by high-vacuum physical techniques. Therefore, many of them have not been prepared as thin films until now. Here we report the synthesis of high-quality epitaxial thin films of the most representative members of this family of compounds by a water-based chemical solution deposition method. The films show an exceptional crystalline quality, with an electrical conductivity and thermopower comparable to single crystals. These properties are linked to the epitaxial matching of the rock-salt layers of the structure to the substrate, producing clean interfaces free of amorphous phases. This is an important step forward for the integration of these materials with complementary n-type thermoelectric oxides in multilayer nanostructures.

  10. Electrical properties of chemically prepared nonstoichiometric CuIn(S,Se)2 thin films

    Indian Academy of Sciences (India)

    R H Bari; L A Patil; A Soni; G S Okram

    2007-04-01

    Polycrystalline thin films of copper indium sulphoselenide [CuIn(S,Se)2] were deposited on glass substrate by chemical bath deposition technique. The deposition parameters such as pH, temperature and time were optimized. A set of films having different elemental compositions was prepared by varying Cu/In ratio from 1.87–12.15. The films were characterized by X-ray diffraction (XRD) and energy dispersive X-ray analysis (EDAX). The chemical composition of the CuIn(S,Se)2 was found to be nonstoichiometric. The d.c. conductivities of the films were studied below and near room temperature. The thermo-electric power of the films was also measured and type of semiconductivity was ascertained.

  11. FragIt: A Tool to Prepare Input Files for Fragment Based Quantum Chemical Calculations

    CERN Document Server

    Steinmann, Casper; Hansen, Anne S; Jensen, Jan H

    2012-01-01

    Near linear scaling fragment based quantum chemical calculations are becoming increasingly popular for treating large systems with high accuracy and is an active field of research. However, it remains difficult to set up these calculations without expert knowledge. To facilitate the use of such methods, software tools need to be available for support, setup and lower the barrier of entry for usage by non-experts. We present a fragmentation methodology and accompanying tools called FragIt to help setup these calculations. It uses the SMARTS language to find chemically appropriate substructures in structures and is used to prepare input files for the fragment molecular orbital method in the GAMESS program package. We present patterns of fragmentation for proteins and polysaccharides, specifically D-galactopyranose for use in cyclodextrins.

  12. Preparation of tetragonal CaO-ZrO2 nano-powder by chemical coprecipitation method

    Institute of Scientific and Technical Information of China (English)

    刘建本; 阮建明; 邹俭鹏; 李亚军; 骆锋

    2003-01-01

    With zirconium oxychloride, nitrate of lime and ammonia as raw materials, nano-powder of CaO-ZrO2 was prepared by chemical coprecipitation method. By use of azeotropic distillation processing, chemical coprecipitation precursor was obtained. Phase transformation of the precursor was observed at the temperature of 593.81 ℃ and 1 234.56 ℃ respectively with DTA analyses. Phase structure was analyzed through XRD and Raman spectra. The average particle size of tetragonal zirconium oxide powder was 9.8 and 43.7 nm after calcination at 600 and 1 100 ℃ respectively which was tested by TEM and BET analyses. Furthermore, the influences of the doping of nitrate of lime and the average particle size of zirconium oxide on the stability of tetragonal zirconium oxide were also discussed.

  13. CdS thin films prepared by laser assisted chemical bath deposition

    Energy Technology Data Exchange (ETDEWEB)

    Garcia, L.V.; Mendivil, M.I.; Garcia Guillen, G.; Aguilar Martinez, J.A. [Facultad de Ingenieria Mecanica y Electrica, Universidad Autonoma de Nuevo Leon, Av. Pedro de Alba s/n, Ciudad Universitaria, San Nicolas de los Garza, Nuevo Leon 66450 (Mexico); Krishnan, B. [Facultad de Ingenieria Mecanica y Electrica, Universidad Autonoma de Nuevo Leon, Av. Pedro de Alba s/n, Ciudad Universitaria, San Nicolas de los Garza, Nuevo Leon 66450 (Mexico); CIIDIT – Universidad Autonoma de Nuevo Leon, Apodaca, Nuevo Leon (Mexico); Avellaneda, D.; Castillo, G.A.; Das Roy, T.K. [Facultad de Ingenieria Mecanica y Electrica, Universidad Autonoma de Nuevo Leon, Av. Pedro de Alba s/n, Ciudad Universitaria, San Nicolas de los Garza, Nuevo Leon 66450 (Mexico); Shaji, S., E-mail: sshajis@yahoo.com [Facultad de Ingenieria Mecanica y Electrica, Universidad Autonoma de Nuevo Leon, Av. Pedro de Alba s/n, Ciudad Universitaria, San Nicolas de los Garza, Nuevo Leon 66450 (Mexico); CIIDIT – Universidad Autonoma de Nuevo Leon, Apodaca, Nuevo Leon (Mexico)

    2015-05-01

    Highlights: • CdS thin films by conventional CBD and laser assisted CBD. • Characterized these films using XRD, XPS, AFM, optical and electrical measurements. • Accelerated growth was observed in the laser assisted CBD process. • Improved dark conductivity and good photocurrent response for the LACBD CdS. - Abstract: In this work, we report the preparation and characterization of CdS thin films by laser assisted chemical bath deposition (LACBD). CdS thin films were prepared from a chemical bath containing cadmium chloride, triethanolamine, ammonium hydroxide and thiourea under various deposition conditions. The thin films were deposited by in situ irradiation of the bath using a continuous laser of wavelength 532 nm, varying the power density. The thin films obtained during deposition of 10, 20 and 30 min were analyzed. The changes in morphology, structure, composition, optical and electrical properties of the CdS thin films due to in situ irradiation of the bath were analyzed by atomic force microscopy (AFM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and UV–vis spectroscopy. The thin films obtained by LACBD were nanocrystalline, photoconductive and presented interesting morphologies. The results showed that LACBD is an effective synthesis technique to obtain nanocrystalline CdS thin films having good optoelectronic properties.

  14. CdS thin films prepared by laser assisted chemical bath deposition

    International Nuclear Information System (INIS)

    Highlights: • CdS thin films by conventional CBD and laser assisted CBD. • Characterized these films using XRD, XPS, AFM, optical and electrical measurements. • Accelerated growth was observed in the laser assisted CBD process. • Improved dark conductivity and good photocurrent response for the LACBD CdS. - Abstract: In this work, we report the preparation and characterization of CdS thin films by laser assisted chemical bath deposition (LACBD). CdS thin films were prepared from a chemical bath containing cadmium chloride, triethanolamine, ammonium hydroxide and thiourea under various deposition conditions. The thin films were deposited by in situ irradiation of the bath using a continuous laser of wavelength 532 nm, varying the power density. The thin films obtained during deposition of 10, 20 and 30 min were analyzed. The changes in morphology, structure, composition, optical and electrical properties of the CdS thin films due to in situ irradiation of the bath were analyzed by atomic force microscopy (AFM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and UV–vis spectroscopy. The thin films obtained by LACBD were nanocrystalline, photoconductive and presented interesting morphologies. The results showed that LACBD is an effective synthesis technique to obtain nanocrystalline CdS thin films having good optoelectronic properties

  15. Physical and Chemical Transformation of Hydroxyapatite Nanoparticles in Aqueous Sol after Preparation and in vitro

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    The co-precipitation method followed by ultrasound and heat treatment is a common way to prepare below 100 nm sized hydroxyapatite nanoparticles for biomedical studies and applications. The size and pH value of the obtained calcium phosphate nanoparticles in aqueous sol have a strong impact on the interactions with cells and tissue. The physical and chemical properties of material samples for in vitro and in vivo studies are often assumed to remain constant from the time after fabrication to the actual use. Only little attention is paid to eventual changes of the material over time or due to the different in vitro conditions. In this study, the physical and chemical transformation of calcium phosphate nanoparticles after preparation and in vitro was investigated. As the result showed, dispersed nano sized amorphous calcium phosphate precipitation as well as crystallized hydroxyapatite nanoparticles continue to crystallize even when kept at 4 ℃ leading to declining pH values and particle sizes.Due to the pH buffer in the medium the pH value of the cell culture remained stable after adding 20% nanoparticle sol in vitro. However, hydroxyapatite nanoparticles immediately became unstable in the presents of cell culture medium. The resulting loose agglomerations showed a size of above 500 nm.

  16. Characterization of Korean Red Ginseng (Panax ginseng Meyer): History, preparation method, and chemical composition.

    Science.gov (United States)

    Lee, Sang Myung; Bae, Bong-Seok; Park, Hee-Weon; Ahn, Nam-Geun; Cho, Byung-Gu; Cho, Yong-Lae; Kwak, Yi-Seong

    2015-10-01

    It has been reported that Korean Red Ginseng has been manufactured for 1,123 y as described in the GoRyeoDoGyeong record. The Korean Red Ginseng manufactured by the traditional preparation method has its own chemical component characteristics. The ginsenoside content of the red ginseng is shown as Rg1: 3.3 mg/g, Re: 2.0 mg/g, Rb1: 5.8 mg/g, Rc:1.7 mg/g, Rb2: 2.3 mg/g, and Rd: 0.4 mg/g, respectively. It is known that Korean ginseng generally consists of the main root and the lateral or fine roots at a ratio of about 75:25. Therefore, the red ginseng extract is prepared by using this same ratio of the main root and lateral or fine roots and processed by the historical traditional medicine prescription. The red ginseng extract is prepared through a water extraction (90(°)C for 14-16 h) and concentration process (until its final concentration is 70-73 Brix at 50-60(°)C). The ginsenoside contents of the red ginseng extract are shown as Rg1: 1.3 mg/g, Re: 1.3 mg/g, Rb1: 6.4 mg/g, Rc:2.5 mg/g, Rb2: 2.3 mg/g, and Rd: 0.9 mg/g, respectively. Arginine-fructose-glucose (AFG) is a specific amino-sugar that can be produced by chemical reaction of the process when the fresh ginseng is converted to red ginseng. The content of AFG is 1.0-1.5% in red ginseng. Acidic polysaccharide, which has been known as an immune activator, is at levels of 4.5-7.5% in red ginseng. Therefore, we recommended that the chemical profiles of Korean Red Ginseng made through the defined traditional method should be well preserved and it has had its own chemical characteristics since its traditional development. PMID:26869832

  17. Preparation and chemical crystallographic study of new hydrides and hydro-fluorides of ionic character

    International Nuclear Information System (INIS)

    Within the context of a growing interest in the study of reversible hydrides with the perspective of their application in hydrogen storage, this research thesis more particularly addressed the case of ternary hydrides and fluorides, and of hydro-fluorides. The author reports the development of a method of preparation of alkaline hydrides, of alkaline earth hydrides and of europium hydride, and then the elaboration of ternary hydrides. He addresses the preparation of caesium fluorides and of calcium or nickel fluorides, of Europium fluorides, and of ternary fluorides. Then, he addresses the preparation of hydro-fluorides (caesium, calcium, europium fluorides, and caesium and nickel fluorides). The author presents the various experimental techniques: chemical analysis, radio-crystallographic analysis, volumetric mass density measurement, magnetic measurements, ionic conductivity measurements, Moessbauer spectroscopy, and nuclear magnetic resonance. He reports the crystallographic study of some ternary alkaline and alkaline-earth hydrides (KH-MgH2, RbH-CaH2, CsH-CaH2, RbH-MgH2 and CsH-MgH2) and of some hydro-fluorides (CsCaF2H, EuF2H, CsNiF2H)

  18. [Isolation of chemical constituents from Ziziphora clinopodioides Lam. with recycling preparative high performance liquid chromatography].

    Science.gov (United States)

    Li, Guozhu; Meng, Qingyan; Luo, Bi; Ge, Zhenghong; Liu, Wenjie

    2015-01-01

    The combination of alternate recycling and direct recycling preparative liquid chromatography method was developed for the isolation of chemical constituents from Ziziphora clinopodioides Lam. The crude extract was obtained from Ziziphora clinopodioides Lam. by solvent extraction, column chromatography and reversed-phase (RP) flash chromatography. All the separations were performed with methanol and water as mobile phases and the developed recycling preparative method was used with twin RP columns switched by a two-position ten-way valve for the separation. The mobile phase was recycled in close loop with a two-position six-way valve. The fraction I and fraction II from reversed-phase flash chromatography were selected for the demonstration of separation power of the proposed protocol, and five compounds were obtained from Ziziphora clinopodioides Lam. The isolated five compounds were identified as pinocembrin-7-O-rutinoside, pinocembrin-7-O-rutinoside, acacetin-7-O-rutinoside, picein and protocatechuic acid with nuclear magnetic resonance (NMR). The experimental results showed that the developed preparation method exhibited higher separation efficiency with less mobile phase used than the reported methods, and could be expected as an effective method for the separation of complex natural products, especially the compounds with similar structures. PMID:25958674

  19. High quality antireflective ZnS thin films prepared by chemical bath deposition

    Energy Technology Data Exchange (ETDEWEB)

    Tec-Yam, S.; Rojas, J.; Rejon, V. [Centro de Investigacion y de Estudios Avanzados del IPN, Unidad Merida, Departamento de Fisica Aplicada, Km. 6 Antigua Carretera a Progreso, AP 73-Cordemex, 97310 Merida Yucatan (Mexico); Oliva, A.I., E-mail: oliva@mda.cinvestav.mx [Centro de Investigacion y de Estudios Avanzados del IPN, Unidad Merida, Departamento de Fisica Aplicada, Km. 6 Antigua Carretera a Progreso, AP 73-Cordemex, 97310 Merida Yucatan (Mexico)

    2012-10-15

    Zinc sulfide (ZnS) thin films for antireflective applications were deposited on glass substrates by chemical bath deposition (CBD). Chemical analysis of the soluble species permits to predict the optimal pH conditions to obtain high quality ZnS films. For the CBD, the ZnCl{sub 2}, NH{sub 4}NO{sub 3}, and CS(NH{sub 2}){sub 2} were fixed components, whereas the KOH concentration was varied from 0.8 to 1.4 M. Groups of samples with deposition times from 60 to 120 min were prepared in a bath with magnetic agitation and heated at 90 Degree-Sign C. ZnS films obtained from optimal KOH concentrations of 0.9 M and 1.0 M exhibited high transparency, homogeneity, adherence, and crystalline. The ZnS films presented a band gap energy of 3.84 eV, an atomic Zn:S stoichiometry ratio of 49:51, a transmittance above 85% in the 300-800 nm wavelength range, and a reflectance below 25% in the UV-Vis range. X-ray diffraction analysis revealed a cubic structure in the (111) orientation for the films. The thickness of the films was tuned between 60 nm and 135 nm by controlling the deposition time and KOH concentration. The incorporation of the CBD-ZnS films into ITO/ZnS/CdS/CdTe and glass/Mo/ZnS heterostructures as antireflective layer confirms their high optical quality. -- Highlights: Black-Right-Pointing-Pointer High quality ZnS thin films were prepared by chemical bath deposition (CBD). Black-Right-Pointing-Pointer Better CBD-ZnS films were achieved by using 0.9 M-KOH concentration. Black-Right-Pointing-Pointer Reduction in the reflectance was obtained for ZnS films used as buffer layers.

  20. Preparation of diamond/Cu microchannel heat sink by chemical vapor deposition

    Institute of Scientific and Technical Information of China (English)

    刘学璋; 罗浩; 苏栩; 余志明

    2015-01-01

    A Ti interlayer with thickness about 300 nm was sputtered on Cu microchannels, followed by an ultrasonic seeding with nanodiamond powders. Adherent diamond film with crystalline grains close to thermal equilibrium shape was tightly deposited by hot-filament chemical vapor deposition (HF-CVD). The nucleation and growth of diamond were investigated with micro-Raman spectroscope and field emission scanning electron microscope (FE-SEM) with energy dispersive X-ray detector (EDX). Results show that the nucleation density is found to be up to 1010 cm−2. The enhancement of the nucleation kinetics can be attributed to the nanometer rough Ti interlayer surface. An improved absorption of nanodiamond particles is found, which act as starting points for the diamond nucleation during HF-CVD process. Furthermore, finite element simulation was conducted to understand the thermal management properties of prepared diamond/Cu microchannel heat sink.

  1. A novel colloid probe preparation method based on chemical etching technique

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Several fundamental problems in hydrophobic force measurements using atomic force microscope (AFM) are discussed in this paper. A novel method for colloid probe preparation based on chemical etching technology is proposed, which is specially fit for the unique demands of hydrophobic force measurements by AFM. The features of three different approaches for determining spring constants of rectangular cantilevers, including geometric dimension, Cleveland and Sader methods are compared. The influences of the sizes of the colloids on the measurements of the hydrophobic force curves are investigated. Our experimental results showed that by selecting colloid probe with proper spring constant and tip size, the hydrophobic force and the complete hydrophobic interaction force curve can be measured by using AFM.

  2. Characterization of doped hydrogenated nanocrystalline silicon films prepared by plasma enhanced chemical vapour deposition

    Institute of Scientific and Technical Information of China (English)

    Wang Jin-Liang; Wu Er-Xing

    2007-01-01

    The B-and P-doped hydrogenated nanocrystalline silicon films (nc-Si:H) are prepared by plasma-enhanced chemical vapour deposition (PECVD) .The microstructures of doped nc-Si:H films are carefully and systematically char acterized by using high resolution electron microscopy (HREM) ,Raman scattering,x-ray diffraction (XRD) ,Auger electron spectroscopy (AES) ,and resonant nucleus reaction (RNR) .The results show that as the doping concentration of PH3 increases,the average grain size (d) tends to decrease and the crystalline volume percentage (Xc) increases simultaneously.For the B-doped samples,as the doping concentration of B2H6 increases,no obvious change in the value of d is observed,but the value of Xc is found to decrease.This is especially apparent in the case of heavy B2H6 doped samples,where the films change from nanocrystalline to amorphous.

  3. Characterization of Korean Red Ginseng (Panax ginseng Meyer): History, preparation method, and chemical composition

    OpenAIRE

    Lee, Sang Myung; Bae, Bong-Seok; Park, Hee-Weon; Ahn, Nam-Geun; Cho, Byung-Gu; Cho, Yong-Lae; Kwak, Yi-Seong

    2015-01-01

    It has been reported that Korean Red Ginseng has been manufactured for 1,123 y as described in the GoRyeoDoGyeong record. The Korean Red Ginseng manufactured by the traditional preparation method has its own chemical component characteristics. The ginsenoside content of the red ginseng is shown as Rg1: 3.3 mg/g, Re: 2.0 mg/g, Rb1: 5.8 mg/g, Rc:1.7 mg/g, Rb2: 2.3 mg/g, and Rd: 0.4 mg/g, respectively. It is known that Korean ginseng generally consists of the main root and the lateral or fine ro...

  4. MICROSTRUCTURE OF SiOx:H FILMS PREPARED BY PLASMA ENHANCED CHEMICAL VAPOR DEPOSITION

    Institute of Scientific and Technical Information of China (English)

    MA ZHI-XUN; LIAO XIAN-BO; KONG GUANG-LIN; CHU JUN-HAO

    2000-01-01

    The micro-Raman spectroscopy and infrared (IR) spectroscopy have been performed for the study of the microstructure of amorphous hydrogenated oxidized silicon (a-SiOx:H) films prepared by Plasma Enhanced Chemical Vapor Deposition technique. It is found that a-SiOx :H consists of two phases: an amorphous silicon-rich phase and an oxygen-rich phase mainly comprised of HSi-SiO2 and HSi-O3. The Raman scattering results exhibit that the frequency of TO-like mode of amorphous silicon red-shifts with decreasing size of silicon-rich region. This is related to the quantum confinement effects, similar to the nanocrystalline silicon.

  5. Chemically prepared well-ordered InP(0 0 1) surfaces

    Science.gov (United States)

    Tereshchenko, O. E.; Paget, D.; Chiaradia, P.; Placidi, E.; Bonnet, J. E.; Wiame, F.; Taleb-Ibrahimi, A.

    2006-08-01

    In the present work HCl-isopropanol treated and vacuum annealed InP(0 0 1) surfaces were studied by means of low-energy electron diffraction (LEED), soft X-ray photoemission (SXPS), and reflectance anisotropy (RAS) spectroscopies. The treatment removes the natural oxide and leaves on the surface a physisorbed overlayer containing InCl x and phosphorus. Annealing at 230 °C induces desorption of InCl x overlayer and reveals a P-rich (2 × 1) surface. Subsequent annealing at higher temperature induces In-rich (2 × 4) surface. The structural properties of chemically prepared InP(0 0 1) surfaces were found to be similar to those obtained by decapping of As/P-capped epitaxial layers.

  6. High temperature stability of nanocrystalline anatase powders prepared by chemical vapour synthesis under varying process parameters

    Science.gov (United States)

    Ahmad, Md. Imteyaz; Fasel, Claudia; Mayer, Thomas; Bhattacharya, S. S.; Hahn, Horst

    2011-05-01

    Systematic variation in the high temperature stability of nanocrystalline anatase powders prepared by chemical vapour synthesis (CVS) using titanium (IV) isopropoxide under varying flow rates of oxygen and helium was obtained by progressively shifting the decomposition product from C 3H 6 to CO 2. The as-synthesised powders were characterised by high temperature X-ray diffraction (HTXRD), simultaneous thermo-gravimetric analyses (STA), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR) and transmission electron microscopy (TEM). It was observed that the anatase to rutile transformation temperature progressively increased for samples synthesised at higher O 2/He flow rate ratios. The improved anatase stability was attributed to the presence of incorporated carbon within the titania structure and confirmed by a high temperature carbon desorption peak.

  7. High temperature stability of nanocrystalline anatase powders prepared by chemical vapour synthesis under varying process parameters

    Energy Technology Data Exchange (ETDEWEB)

    Ahmad, Md. Imteyaz [Materials Testing Facility, Materials Forming Laboratory, Department of Metallurgical and Materials Engineering, Indian Institute of Technology Madras, Chennai 600036 (India); Joint Research Laboratory Nanomaterials, Technische Universitaet Darmstadt and Forschungszentrum Karlsruhe, 64287 Darmstadt (Germany); Fasel, Claudia [Disperse Feststoffe, Institute of Materials Science, Darmstadt University of Technology, 64287 Darmstadt (Germany); Mayer, Thomas [Oberflaechenforschung, Institute of Materials Science, Darmstadt University of Technology, 64287 Darmstadt (Germany); Bhattacharya, S.S., E-mail: ssb@iitm.ac.in [Materials Testing Facility, Materials Forming Laboratory, Department of Metallurgical and Materials Engineering, Indian Institute of Technology Madras, Chennai 600036 (India); Hahn, Horst [Joint Research Laboratory Nanomaterials, Technische Universitaet Darmstadt and Forschungszentrum Karlsruhe, 64287 Darmstadt (Germany)

    2011-05-15

    Systematic variation in the high temperature stability of nanocrystalline anatase powders prepared by chemical vapour synthesis (CVS) using titanium (IV) isopropoxide under varying flow rates of oxygen and helium was obtained by progressively shifting the decomposition product from C{sub 3}H{sub 6} to CO{sub 2}. The as-synthesised powders were characterised by high temperature X-ray diffraction (HTXRD), simultaneous thermo-gravimetric analyses (STA), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR) and transmission electron microscopy (TEM). It was observed that the anatase to rutile transformation temperature progressively increased for samples synthesised at higher O{sub 2}/He flow rate ratios. The improved anatase stability was attributed to the presence of incorporated carbon within the titania structure and confirmed by a high temperature carbon desorption peak.

  8. Synthesis and spectroscopic characterization of gold nanobipyramids prepared by a chemical reduction method

    Science.gov (United States)

    Thanh Ngo, Vo Ke; Phat Huynh, Trong; Giang Nguyen, Dang; Phuong Uyen Nguyen, Hoang; Lam, Quang Vinh; Dat Huynh, Thanh

    2015-12-01

    Gold nanobipyramids (NBPs) have attracted much attention because they have potential for applications in smart sensing devices, such as medical diagnostic equippments. This is due to the fact that they show more advantageous plasmonic properties than other gold nanostructures. We describe a chemical reduction method for synthesizing NBPs using conventional heating with ascorbic acid reduction and cetyltrimethylamonium bromide (CTAB) + AgNO3 as capping agents. The product was characterized by ultraviolet-visible spectroscopy (UV-vis), Fourier transmission infrared spectroscopy (FTIR), transmission electron microscopy (TEM), x-ray powder diffraction (XRD). The results showed that gold nanoparticles were formed with bipyramid shape (tip-to-tip distance of 88.4 ± 9.4 nm and base length of 29.9 ± 3.2 nm) and face-centered-cubic crystalline structure. Optimum parameters for preparation of NBPs are also found.

  9. Highly sensitive methanol chemical sensor based on undoped silver oxide nanoparticles prepared by a solution method

    International Nuclear Information System (INIS)

    We have prepared silver oxide nanoparticles (NPs) by a simple solution method using reducing agents in alkaline medium. The resulting NPs were characterized by UV-vis and FT-IR spectroscopy, X-ray powder diffraction, and field-emission scanning electron microscopy. They were deposited on a glassy carbon electrode to give a sensor with a fast response towards methanol in liquid phase. The sensor also displays good sensitivity and long-term stability, and enhanced electrochemical response. The calibration plot is linear (r2 = 0.8294) over the 0.12 mM to 0.12 M methanol concentration range. The sensitivity is ∼ 2.65 μAcm-2 mM-1, and the detection limit is 36.0 μM (at a SNR of 3). We also discuss possible future prospective uses of this metal oxide semiconductor nanomaterial in terms of chemical sensing. (author)

  10. Effect of Organic Solvents in Preparation of Silica-Based Chemical Gel Decontaminates for Decontamination of Nuclear Facilities

    International Nuclear Information System (INIS)

    Decontamination of nuclear facilities is necessary to reduce the radiation field during normal operations and decommissioning of complex equipment such as stainless steel components, other iron-based steel and alloys, metal surfaces, structural materials and so on. Chemical decontamination technology in particular is a highly effective method to remove the radioactive contamination through a chemical dissolution or a redox reaction. However, this method has the serious drawback due to the generation of large amounts of the radioactive liquid wastes. Recently, a few literatures have been reported for the preparation of the chemical gel decontaminants to reduce the amount of the radioactive liquid wastes and to enhance the decontamination efficiency through increasing the contact time between the gels and the radioactive contaminants. In the preparation of the chemical gels, the control of the viscosity highly depends on the amount of a coviscosifier used among the components of the chemical gels consisted of a viscosifier, a coviscosifier, and a chemical decontaminant. In this works, a new effective method for the preparation of the chemical gel was investigated by introducing the organic solvents. The mixture solution of the coviscosifier and organic solvent was more effective in the control of the viscosity compared with that of the coviscosifier only in gels. Furthermore, the decontamination efficiency of the chemical gels measured by using the multi-channel analyzer (MCA) showed the high decontamination factor for Co-60 and Cs-137 contaminated on the surface of the stainless steel 304

  11. Effect of Organic Solvents in Preparation of Silica-Based Chemical Gel Decontaminates for Decontamination of Nuclear Facilities

    Energy Technology Data Exchange (ETDEWEB)

    Yoon, Suk Bon; Jung, Chong Hun; Kim, Chang Ki; Choi, Byung Seon; Lee, Kune Woo; Moon, Jei Kwon [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2011-10-15

    Decontamination of nuclear facilities is necessary to reduce the radiation field during normal operations and decommissioning of complex equipment such as stainless steel components, other iron-based steel and alloys, metal surfaces, structural materials and so on. Chemical decontamination technology in particular is a highly effective method to remove the radioactive contamination through a chemical dissolution or a redox reaction. However, this method has the serious drawback due to the generation of large amounts of the radioactive liquid wastes. Recently, a few literatures have been reported for the preparation of the chemical gel decontaminants to reduce the amount of the radioactive liquid wastes and to enhance the decontamination efficiency through increasing the contact time between the gels and the radioactive contaminants. In the preparation of the chemical gels, the control of the viscosity highly depends on the amount of a coviscosifier used among the components of the chemical gels consisted of a viscosifier, a coviscosifier, and a chemical decontaminant. In this works, a new effective method for the preparation of the chemical gel was investigated by introducing the organic solvents. The mixture solution of the coviscosifier and organic solvent was more effective in the control of the viscosity compared with that of the coviscosifier only in gels. Furthermore, the decontamination efficiency of the chemical gels measured by using the multi-channel analyzer (MCA) showed the high decontamination factor for Co-60 and Cs-137 contaminated on the surface of the stainless steel 304

  12. Octafluorodirhenate(III) Revisited: Solid-State Preparation, Characterization, and Multiconfigurational Quantum Chemical Calculations.

    Science.gov (United States)

    Mariappan Balasekaran, Samundeeswari; Todorova, Tanya K; Pham, Chien Thang; Hartmann, Thomas; Abram, Ulrich; Sattelberger, Alfred P; Poineau, Frederic

    2016-06-01

    A simple method for the high-yield preparation of (NH4)2[Re2F8]·2H2O has been developed that involves the reaction of (n-Bu4N)2[Re2Cl8] with molten ammonium bifluoride (NH4HF2). Using this method, the new salt [NH4]2[Re2F8]·2H2O was prepared in ∼90% yield. The product was characterized in solution by ultraviolet-visible light (UV-vis) and (19)F nuclear magnetic resonance ((19)F NMR) spectroscopies and in the solid-state by elemental analysis, powder X-ray diffraction (XRD), and infrared (IR) spectroscopy. Multiconfigurational CASSCF/CASPT2 quantum chemical calculations were performed to investigate the molecular and electronic structure, as well as the electronic absorption spectrum of the [Re2F8](2-) anion. The metal-metal bonding in the Re2(6+) unit was quantified in terms of effective bond order (EBO) and compared to that of its [Re2Cl8](2-) and [Re2Br8](2-) analogues. PMID:27171734

  13. Preparation of Al2O3/Mo nanocomposite powder via chemical route and spray drying

    International Nuclear Information System (INIS)

    A route to prepare nanometer-sized Mo particulates in Al2O3 was attempted by a combination of solution reactions in molecular scale and forcing precipitation by a spray-drying technique. MoO3 was first dissolved in ammonia water and then added in the slurry with high purity, submicrometer Al2O3 powder. Mixed suspension was spray-dried, and then the dried granules were reduced by hydrogen gas and further hot-pressing to a bulky composite at various temperatures. Dissolution of Mo oxide, adsorption reactions on alumina surface, and surface potential of alumina particles in homogeneous ammonia suspension were studied. Characterization of the granules, including compactability, flowing properties, surface morphology, grain growth of Mo and Al2O3, and mixing homogeneity, were examined. Homogeneity of the spray-dried granules was determined by the calculation of mixing index and the observation of the microstructure of sintered body. The existence of intergranular, intragranular, and nanosized Mo particulates within Al2O3 grains was observed by transmission electron microscopy (TEM). All the evidences revealed that homogeneous composites with nanometer-sized Mo had been successfully prepared by this attempt with the proposed chemical route and following spray-drying process. copyright 1996 Materials Research Society

  14. Characterization of mesoporous carbon prepared from date stems by H3PO4 chemical activation

    International Nuclear Information System (INIS)

    The present work was focused on the determination of texture, morphology, crystanillity and oxygenated surface groups characteristics of an activated carbon prepared from date stems. Chemical activation of this precursor at different temperatures (450, 550 and 650 °C) was adopted using phosphoric acid as dehydrating agent at (2/1) impregnation ratio. Fourier transform infrared spectroscopy study was carried out to identify surface groups in date stems activated carbons. The microscopic structure was examined by nitrogen adsorption at 77 K. The interlayer spacing (d200 and d100), stack height (Lc), stack width (La) and effective dimension L of the turbostratic crystallites (microcrystallite) in the date stems activated carbons were estimated from X-ray diffraction data (XRD). Results yielded a surface area, SBET, and total pore volume of 682, 1455, 1319 m2/g and 0,343, 1,045 and 0.735 cm3/g, for the carbon prepared at 450, 550 and 650 °C, respectively. Scanning electron microscopy exhibits a highly developed porosity which is in good agreement with the porous texture derived from gas adsorption data and these results confirm that the activated carbon is dominated by network of slit-shaped mesopores morphology and in some cases by varied micropores morphologies.

  15. Morphology of CdSe films prepared by chemical bath deposition: The role of substrate

    Energy Technology Data Exchange (ETDEWEB)

    Simurda, M. [Charles University in Prague, Faculty of Mathematics and Physics, Ke Karlovu 3, 121 16 Prague 2 (Czech Republic); Nemec, P. [Charles University in Prague, Faculty of Mathematics and Physics, Ke Karlovu 3, 121 16 Prague 2 (Czech Republic)]. E-mail: nemec@karlov.mff.cuni.cz; Formanek, P. [Institut fuer Strukturphysik, Technische Universitaet Dresden, Zellescher Weg 16, D-01062 Dresden (Germany); Nemec, I. [Charles University in Prague, Faculty of Science, Albertov 6, 128 43 Prague 2 (Czech Republic); Nemcova, Y. [Charles University in Prague, Faculty of Science, Albertov 6, 128 43 Prague 2 (Czech Republic); Maly, P. [Charles University in Prague, Faculty of Mathematics and Physics, Ke Karlovu 3, 121 16 Prague 2 (Czech Republic)

    2006-07-26

    We combine optical spectroscopy and transmission electron microscopy to study the growth and the structural morphology of CdSe films prepared by chemical bath deposition (CBD) on two considerably different substrates. The films grown on glass are compact and strongly adherent to the substrate. On the contrary, the films deposited on carbon-coated glass (with approx. 20 nm thick amorphous carbon layer) are only loosely adherent to the substrate. Using transmission electron microscopy we revealed that even though the films grown on both substrates are assembled from closely spaced nanocrystals with diameter of about 5 nm, the films morphology on the sub-micrometer scale is considerably different in the two cases. While the films deposited on glass are rather compact, the films prepared on carbon layer have high porosity and are formed by interconnected spheres which size is dependent on the duration of deposition (e.g. 155 nm for 6 h and 350 nm for 24 h). This shows that the choice of the substrate for CBD has a stronger influence on the sub-micrometer film morphology than on the properties of individual nanocrystals forming the film.

  16. Morphology of CdSe films prepared by chemical bath deposition: The role of substrate

    International Nuclear Information System (INIS)

    We combine optical spectroscopy and transmission electron microscopy to study the growth and the structural morphology of CdSe films prepared by chemical bath deposition (CBD) on two considerably different substrates. The films grown on glass are compact and strongly adherent to the substrate. On the contrary, the films deposited on carbon-coated glass (with approx. 20 nm thick amorphous carbon layer) are only loosely adherent to the substrate. Using transmission electron microscopy we revealed that even though the films grown on both substrates are assembled from closely spaced nanocrystals with diameter of about 5 nm, the films morphology on the sub-micrometer scale is considerably different in the two cases. While the films deposited on glass are rather compact, the films prepared on carbon layer have high porosity and are formed by interconnected spheres which size is dependent on the duration of deposition (e.g. 155 nm for 6 h and 350 nm for 24 h). This shows that the choice of the substrate for CBD has a stronger influence on the sub-micrometer film morphology than on the properties of individual nanocrystals forming the film

  17. Femtosecond Transient Absorption Studies in Cadmium Selenide Nanocrystal Thin Films Prepared by Chemical Bath Deposition Method

    Directory of Open Access Journals (Sweden)

    M. C. Rath

    2007-01-01

    Full Text Available Dynamics of photo-excited carrier relaxation processes in cadmium selenide nanocrystal thin films prepared by chemical bath deposition method have been studied by nondegenerate femtosecond transient pump-probe spectroscopy. The carriers were generated by exciting at 400 nm laser light and monitored by several other wavelengths. The induced absorption followed by a fast bleach recovery observed near and above the bandgap indicates that the photo-excited carriers (electrons are first trapped by the available traps and then the trapped electrons absorb the probe light to show a delayed absorption process. The transient decay kinetics was found to be multiexponential in nature. The short time constant, <1 picosecond, was attributed to the trapping of electrons by the surface and/or deep traps and the long time constant, ≥20 picoseconds, was due to the recombination of the trapped carriers. A very little difference in the relaxation processes was observed in the samples prepared at bath temperatures from 25∘C to 60∘C.

  18. YBCO coated conductors prepared by chemical solution deposition: A TEM study

    International Nuclear Information System (INIS)

    Recently large attention has been devoted to chemical solution deposition (CSD) as a promising method for fabricating low-cost YBCO coated conductors. We present an extensive transmission electron microscopy (TEM) cross-section analysis of CSD grown La2Zr2O7 (LZO) buffer layers on flexible Ni-5at%W substrates. The high performance of these chemical solution derived buffer layers was confirmed by a YBCO critical current density Jc of 0.84 MA/cm2 achieved for a coated conductor sample with a layer sequence Ni-5at%W/LZO (CSD)/CeO2 (CSD)/YBCO, where the YBCO film was deposited by pulsed laser deposition (PLD). TEM sample preparation was carried out by conventional mechanical polishing and ion milling techniques. TEM bright-field images of the LZO films and nickel substrates were acquired under two-beam conditions. The layer thicknesses and nanovoid size were determined for the LZO buffer layers. Moreover, the interfaces between the different layers were investigated and identified. Electron diffraction patterns were obtained in order to determine the microscopic texture of the samples. Despite the presence of nanovoids in the LZO buffer layers, they act as efficient Ni diffusion barriers

  19. Antibacterial, Structural and Optical Characterization of Mechano-Chemically Prepared ZnO Nanoparticles

    Science.gov (United States)

    Bokhari, Habib; Ahmad, Iftikhar

    2016-01-01

    Structural investigations, optical properties and antibacterial performance of the pure Zinc Oxide (ZnO) nanoparticles (NPs) synthesized by mechano-chemical method are presented. The morphology, dimensions and crystallinity of the ZnO NPs were controlled by tweaking the mechanical agitation of the mixture and subsequent thermal treatment. ZnO nanoparticles in small (< 20 nm) dimensions with spherical morphology and narrow size distribution were successfully obtained after treating the mechano-chemically prepared samples at 250°C. However, higher temperature treatments produced larger particles. TEM, XRD and UV-Vis spectroscopy results suggested crystalline and phase pure ZnO. The NPs demonstrated promising antibacterial activity against Gram negative foodborne and waterborne bacterial pathogens i.e. Enteropathogenic E. coli (EPEC), Campylobacter jejuni and Vibrio cholerae as well as Gram positive methicillin resistant Staphylococcus aureus (MRSA), thus potential for medical applications. Scanning electron microscopy and survival assay indicated that most probably ZnO nanoparticles cause changes in cellular morphology which eventually causes bacterial cell death. PMID:27183165

  20. Structure and composition of chemically prepared and vacuum annealed InSb(0 0 1) surfaces

    Science.gov (United States)

    Tereshchenko, O. E.

    2006-08-01

    The InSb(0 0 1) surfaces chemically treated in HCl-isopropanol solution and annealed in vacuum were studied by means of X-ray photoelectron spectroscopy (XPS), low energy electron diffraction (LEED) and electron energy-loss spectroscopy (EELS). The HCl-isopropanol treatment removes indium and antimony oxides and leaves on the surface about 3 ML of physisorbed overlayer, containing indium chlorides and small amounts of antimony, which can be thermally desorbed at 230 °C. The residual carbon contaminations were around 0.2-0.4 ML and consisted of the hydrocarbon molecules. These hydrocarbon contaminations were removed from the surface together with the indium chlorides and antimony overlayer. With increased annealing temperature, a sequence of reconstructions were identified by LEED: (1 × 1), (1 × 3), (4 × 3), and (4 × 1)/c(8 × 2), in the order of decreasing Sb/In ratio. The structural properties of chemically prepared InSb(0 0 1) surface were found to be similar to those obtained by decapping of Sb-capped epitaxial layers.

  1. Preparation of High Impermeable and Crack-resistance Chemical Admixture and Its Mechanism

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    A kind of high impermeable and crack-resistance chemical admixture (HICRCA) was prepared, which is a compound chemical admixture composed of an expansion ingredient,density ingredient, and organic hydrophobic poreblocking ingredient. The results of the experiments indicate that the addition of HICRCA improves mortar and concrete in the following performances:(1) perfect workability: slump is more than 22cm, the slump after 3h is about 16cm; (2)high impermeability:for the mortar,the pervious height under a water pressure of 1.5MPa is 1.5cm,for the concrete, the pervious height under a water pressure of 5.0MPa is 2.2cm;(3)high crack-resistance:there is a micro-expansion at the age of 90d;(4)high compressivestrength:compared with the controlled concrete,the compressive strengths at the age of 3d and 28d are improved by 66.4% and 62.0%, respectively.At the same time,the effects of different curing condition on mortar and concrete expansive and shrinkage performance were studied.In addition,the impermeable and crack-resistance mechanism was investigated in the present paper.

  2. Chemical and biological assessment of Angelica herbal decoction: comparison of different preparations during historical applications.

    Science.gov (United States)

    Zhang, Wendy Li; Zheng, Ken Yu-Zhong; Zhu, Kevin Yue; Zhan, Janis Ya-Xian; Bi, Cathy Wen-Chuan; Chen, Jian-Ping; Du, Crystal Ying-Qing; Zhao, Kui-Jun; Lau, David Tai-Wai; Dong, Tina Ting-Xia; Tsim, Karl Wah-Keung

    2012-08-15

    The commonly used Angelica herbal decoction today is Danggui Buxue Tang (DBT), which is a dietary supplement in treating menopausal irregularity in women, i.e. to nourish "Qi" and to enrich "Blood". According to historical record, many herbal decoctions were also named DBT, but the most popular formulation of DBT was written in Jin dynasty (1247 AD) of China, which contained Astragali Radix (AR) and Angelicae Sinensis Radix (ASR) with a weight ratio of 5:1. However, at least two other Angelica herbal decoctions recorded as DBT were prescribed in Song (1155 AD) and Qing dynasties (1687 AD). Although AR and ASR are still the major components in the DBT herbal decoctions, they are slightly varied in the herb composition. In order to reveal the efficiency of different Angelica herbal decoctions, the chemical and biological properties of three DBT herbal extracts were compared. Significantly, the highest amounts of AR-derived astragaloside III, astragaloside IV, calycosin and formononetin and ASR-derived ferulic acid were found in DBT described in 1247 AD: this preparation showed stronger activities in osteogenic, estrogenic and erythropoetic effects than the other two DBT. The current results supported the difference of three DBT in chemical and biological properties, which could be a result of different herbal combinations. For the first time, this study supports the popularity of DBT described in 1247 AD. PMID:22902230

  3. Preparation of conductive polypyrrole/polyurethane foams and their application as chemical sensors

    Science.gov (United States)

    Wang, Yanbing

    Electrically conductive polypyrrole/polyurethane (PPy/PU) composite foams were prepared by first impregnating the PU foams with iodine, and then exposing the iodine-loaded PU foams to pyrrole vapor, which resulted in the in situ oxidative polymerization of pyrrole monomer by iodine oxidant. Iodine sorption by polyurethane (PU) and melamine-formaldehyde (MF) foams was studied using both iodine sublimation and iodine solutions with hexanes and toluene. In the sublimation process, the diffusion kinetics was investigated and the interaction between iodine and PU foams was characterized by DSC, TGA, Raman spectroscopy and electrical conductivity measurements. In the solution process, the equilibrium absorption followed the distribution law and the distribution coefficients varied depending on the solvent used. MF foam achieved no iodine absorption in both processes which can be attributed to the lack of charge-transfer interactions. The kinetics, equilibrium and mechanism of the in situ polymerization of pyrrole by iodine in a PU foam was investigated and discussed. The dopant for the PPy was primarily I3-, which formed a charge-transfer complex (PPy-I2) with the amine groups of the PPy. The conductivity of the composite foams was measured and several factors affecting the conductivity were analyzed. The chemical structure, morphology, mechanical properties and thermal stability of the composite foams, and the relationships between these factors were characterized. The PPy/PU composite foams were investigated as sensors for various volatile chemicals, including some chemical warfare simulants. High sensitivity has been demonstrated for organic amine compounds, as well as two mustard agent simulants. The quasireversibility and time scale of the resistance response was qualitatively explained based on the mass uptake characteristic of amine by the composite foam. Humidity also demonstrated its influence on the resistance of the foam sensor in a completely reversible

  4. Adsorption studies of methylene blue and phenol onto vetiver roots activated carbon prepared by chemical activation

    International Nuclear Information System (INIS)

    Vetiver roots have been utilized for the preparation of activated carbon (AC) by chemical activation with different impregnation ratios of phosphoric acid, XP (g H3PO4/g precursor): 0.5:1; 1:1 and 1.5:1. Textural characterization, determined by nitrogen adsorption at 77 K shows that mixed microporous and mesoporous structures activated carbons (ACs) with high surface area (>1000 m2/g) and high pore volume (up to 1.19 cm3/g) can be obtained. The surface chemical properties of these ACs were investigated by X-ray photoelectron spectroscopy (XPS) and Boehm titration. Their textural and chemical characteristics were compared to those of an AC sample obtained by steam activation of vetiver roots. Classical molecules used for characterizing liquid phase adsorption, phenol and methylene blue (MB), were used. Adsorption kinetics of MB and phenol have been studied using commonly used kinetic models, i.e., the pseudo-first-order model, the pseudo-second-order model, the intraparticle diffusion model and as well the fractal, BWS (Brouers, Weron and Sotolongo) kinetic equation. The correlation coefficients (R2) and the normalized standard deviation Δq (%) were determined showing globally, that the recently derived fractal kinetic equation could best describe the adsorption kinetics for the adsorbates tested here, indicating a complex adsorption mechanism. The experimental adsorption isotherms of these molecules on the activated carbon were as well analysed using four isotherms: the classical Freundlich, Langmuir, Redlich-Peterson equations, but as well the newly published deformed Weibull Brouers-Sotolongo isotherm. The results obtained from the application of the equations show that the best fits were achieved with the Brouers-Sotolongo equation and with the Redlich-Peterson equation. Influence of surface functional groups towards MB adsorption is as well studied using various ACs prepared from vetiver roots and sugar cane bagasse. Opposite effects governing MB and phenol

  5. Adsorption studies of methylene blue and phenol onto vetiver roots activated carbon prepared by chemical activation

    Energy Technology Data Exchange (ETDEWEB)

    Altenor, Sandro [COVACHIMM, EA 3592 Universite des Antilles et de la Guyane, BP 250, 97157 Pointe a Pitre Cedex, Guadeloupe (France); LAQUE, Universite Quisqueya d' Haiti, Port-au-Prince (Haiti); Carene, Betty [COVACHIMM, EA 3592 Universite des Antilles et de la Guyane, BP 250, 97157 Pointe a Pitre Cedex, Guadeloupe (France); Emmanuel, Evens [LAQUE, Universite Quisqueya d' Haiti, Port-au-Prince (Haiti); Lambert, Jacques; Ehrhardt, Jean-Jacques [Laboratoire de Chimie Physique et Microbiologie pour l' Environnement, UMR 7564 CNRS-Nancy Universities, 405 rue de Vandoeuvre, F 54600 Villers-les-Nancy Cedex (France); Gaspard, Sarra, E-mail: sgaspard@univ-ag.fr [COVACHIMM, EA 3592 Universite des Antilles et de la Guyane, BP 250, 97157 Pointe a Pitre Cedex, Guadeloupe (France)

    2009-06-15

    Vetiver roots have been utilized for the preparation of activated carbon (AC) by chemical activation with different impregnation ratios of phosphoric acid, X{sub P} (g H{sub 3}PO{sub 4}/g precursor): 0.5:1; 1:1 and 1.5:1. Textural characterization, determined by nitrogen adsorption at 77 K shows that mixed microporous and mesoporous structures activated carbons (ACs) with high surface area (>1000 m{sup 2}/g) and high pore volume (up to 1.19 cm{sup 3}/g) can be obtained. The surface chemical properties of these ACs were investigated by X-ray photoelectron spectroscopy (XPS) and Boehm titration. Their textural and chemical characteristics were compared to those of an AC sample obtained by steam activation of vetiver roots. Classical molecules used for characterizing liquid phase adsorption, phenol and methylene blue (MB), were used. Adsorption kinetics of MB and phenol have been studied using commonly used kinetic models, i.e., the pseudo-first-order model, the pseudo-second-order model, the intraparticle diffusion model and as well the fractal, BWS (Brouers, Weron and Sotolongo) kinetic equation. The correlation coefficients (R{sup 2}) and the normalized standard deviation {Delta}q (%) were determined showing globally, that the recently derived fractal kinetic equation could best describe the adsorption kinetics for the adsorbates tested here, indicating a complex adsorption mechanism. The experimental adsorption isotherms of these molecules on the activated carbon were as well analysed using four isotherms: the classical Freundlich, Langmuir, Redlich-Peterson equations, but as well the newly published deformed Weibull Brouers-Sotolongo isotherm. The results obtained from the application of the equations show that the best fits were achieved with the Brouers-Sotolongo equation and with the Redlich-Peterson equation. Influence of surface functional groups towards MB adsorption is as well studied using various ACs prepared from vetiver roots and sugar cane bagasse

  6. Adsorption studies of methylene blue and phenol onto vetiver roots activated carbon prepared by chemical activation.

    Science.gov (United States)

    Altenor, Sandro; Carene, Betty; Emmanuel, Evens; Lambert, Jacques; Ehrhardt, Jean-Jacques; Gaspard, Sarra

    2009-06-15

    Vetiver roots have been utilized for the preparation of activated carbon (AC) by chemical activation with different impregnation ratios of phosphoric acid, X(P) (gH(3)PO(4)/g precursor): 0.5:1; 1:1 and 1.5:1. Textural characterization, determined by nitrogen adsorption at 77K shows that mixed microporous and mesoporous structures activated carbons (ACs) with high surface area (>1000 m(2)/g) and high pore volume (up to 1.19 cm(3)/g) can be obtained. The surface chemical properties of these ACs were investigated by X-ray photoelectron spectroscopy (XPS) and Boehm titration. Their textural and chemical characteristics were compared to those of an AC sample obtained by steam activation of vetiver roots. Classical molecules used for characterizing liquid phase adsorption, phenol and methylene blue (MB), were used. Adsorption kinetics of MB and phenol have been studied using commonly used kinetic models, i.e., the pseudo-first-order model, the pseudo-second-order model, the intraparticle diffusion model and as well the fractal, BWS (Brouers, Weron and Sotolongo) kinetic equation. The correlation coefficients (R(2)) and the normalized standard deviation Deltaq (%) were determined showing globally, that the recently derived fractal kinetic equation could best describe the adsorption kinetics for the adsorbates tested here, indicating a complex adsorption mechanism. The experimental adsorption isotherms of these molecules on the activated carbon were as well analysed using four isotherms: the classical Freundlich, Langmuir, Redlich-Peterson equations, but as well the newly published deformed Weibull Brouers-Sotolongo isotherm. The results obtained from the application of the equations show that the best fits were achieved with the Brouers-Sotolongo equation and with the Redlich-Peterson equation. Influence of surface functional groups towards MB adsorption is as well studied using various ACs prepared from vetiver roots and sugar cane bagasse. Opposite effects governing MB

  7. Preparation of TiC/W core–shell structured powders by one-step activation and chemical reduction process

    International Nuclear Information System (INIS)

    Highlights: • A novel wet chemical method was used to prepare TiC/W core–shell structure powders. • TiC nanoparticles were well-encapsulated by W shells. • TiC phase was present in the interior of tungsten grains. - Abstract: In the present study, one-step activation and chemical reduction process as a novel wet-chemical route was performed for the preparation of TiC/W core–shell structured ultra-fine powders. The XRD, FE-SEM, TEM and EDS results demonstrated that the as-synthesized powders are of high purity and uniform with a diameter of approximately 500 nm. It is also found that the TiC nanoparticles were well-encapsulated by W shells. Such a unique process suggests a new method for preparing X/W (X refers the water-insoluble nanoparticles) core–shell nanoparticles with different cores

  8. Preparation and Determination of the Physical and Chemical Properties of Margarine

    Directory of Open Access Journals (Sweden)

    Habazin, S.

    2012-02-01

    Full Text Available Nutrition is one of the most basic needs of the human body. It ensures the introduction of substances needed to sustain life of the organism, its growth and proper development. In the food pyramid, fats together with carbohydrates are at the very top. One source of fat in human nutrition is margarine. Margarine comprises at least 82 % vegetable fats and 16 % water. The remainder consists of lecithin, sugar, salt, colours, and vitamins.The margarine production process involves hydrogenation of vegetable fats, assembling the margarine mixture, emulsifying, crystallization and packing.The objective of this study was to show that margarine could be prepared in a school laboratory under conditions that are applicable for such laboratory. Meaning:a In a school laboratory at normal pressure and at elevated temperature with nickel as catalyst, i.e. without the use of an autoclave, carry out the reaction of hydrogenation soybean and palm oil in order to obtain a vegetable fat that is the basic ingredient of margarine. During the preparation of margarine, the hydrogenation reaction was carefully monitored by determining the iodine value.b Preparation of margarine obtained from vegetable fats.c Determination and comparison of selected physical and chemical properties of the product with the same properties of several types of margarines available on the market. The following properties were determined:– Melting point, in order to obtain composition of fat phase and determine suitability for humanuse.– Acid value, as an indicator of the amount of free fatty acids that influence the taste.– Peroxide value, for insight into the oxidative stability of fats.This work has shown that it is possible to make vegetable fat in a school lab by hydrogenation of vegetable oils. Unlike the industrial process of hydrogenation carried out under a pressure of 0.36 to 2 atm, which takes about two hours, our reaction was carried out at atmospheric pressure but with a

  9. Identification of chemicals relevant to the Chemical Weapons Convention using the novel sample-preparation methods and strategies of the Mobile Laboratory of the Organization for the Prohibition of Chemical Weapons

    NARCIS (Netherlands)

    O. Terzic; H. Gregg; P. de Voogt

    2014-01-01

    The standard approach to on-site sample preparation for gas chromatography-mass spectrometry analysis of chemicals relevant to the Chemical Weapons Convention provides relatively good coverage of the target analytes, but it suffers from a number of drawbacks, such as low sample throughput, use of bu

  10. Physical chemical and citotoxic evaluation of highly diluted solutions of Euphorbia tirucalli L. prepared through the fifty milesimal homeopathic method

    Directory of Open Access Journals (Sweden)

    Carlos Renato Zacharias

    2010-07-01

    Full Text Available Background: although Hahnemann described the fifty-milesimal (LM method in the 6th edition of the Organon of the Medical Art, very little research has been carried out on the physical chemical properties of these homeopathic preparations. Furthermore, there is still no evidence allowing for the correlation between the alleged physical chemical properties and the biological effects of high dilutions. Aims: to evaluate physical chemical characteristics of LM preparations including electrical conductivity, pH and refraction index, and their effect on biological experimental models. Materials and methods: preparations tested for physical chemical analysis were dilutions 1 lm to 10 lm of Euphorbia tirucalli L. prepared from the latex and the juice of the plant. To rule the seasonal characteristics of this plant, 2 different populations were used, one collected in June 2007 and the other in May 2008. Furthermore, the cytotoxic effect of Euphorbia tirucalli 5 lm was tested on human breast cancer cells (MCF7 through MTT assay. Some differences among the two collections were observed. However, any clear correlation could be observed between physical chemical properties and biological activity.

  11. 1,5-Anhydro-D-fructose: biocatalytic and chemical synthetic methods for the preparation, transformation and derivatization

    DEFF Research Database (Denmark)

    Lundt, Inge; Yu, Shukun

    2010-01-01

    1,5-Anhydro-D-fructose (1,5AnFru) is a monoketosaccharide that can be prepared enzymatically from starch by a-1,4-glucan lyase or chemically from D-glucose or D-fructose in a few steps with high yields. The formed 1,5AnFru can be derivatized both enzymatically and chemically to interesting new...

  12. Octafluorodirhenate(III) Revisited: Solid-State Preparation, Characterization, and Multiconfigurational Quantum Chemical Calculations

    Energy Technology Data Exchange (ETDEWEB)

    Mariappan Balasekaran, Samundeeswari; Todorova, Tanya K.; Pham, Chien Thang; Hartmann, Thomas; Abram, Ulrich; Sattelberger, Alfred P.; Poineau, Frederic

    2016-06-06

    A simple method for the high-yield preparation of (NH4)2[Re2F8]· 2H2O has been developed that involves the reaction of (n-Bu4N)2[Re2Cl8] with molten ammonium bifluoride (NH4HF2). Using this method, the new salt [NH4]2[Re2F8]·2H2O was prepared in ~90% yield. The product was characterized in solution by ultraviolet-visible light (UV-vis) and 19F nuclear magnetic resonance (19F NMR) spectroscopies and in the solid-state by elemental analysis, powder X-ray diffraction (XRD), and infrared (IR) spectroscopy. Multiconfigurational CASSCF/CASPT2 quantum chemical calculations were performed to investigate the molecular and electronic structure, as well as the electronic absorption spectrum of the [Re2F8] 2- anion. The metal-metal bonding in the Re2 6+ unit was quantified in terms of effective bond order (EBO) and compared to that of its [Re2Cl8] 2- and [Re2Br8] 2- analogues.

  13. YBa2Cu3O7-x thin films prepared by chemical solution deposition

    International Nuclear Information System (INIS)

    The discovery of superconductivity in ceramic materials by Bednorz and Mueller in early 1987, immediately followed by Wu et al., who showed that YBa2Cu3O7-x (YBCO) becomes superconducting (92 K) well above the boiling point of nitrogen (77 K) created a great excitement in superconductivity research. Potential applications of high Tc-superconductors require large critical currents and high-applied magnetic fields. Effective ways to increase the critical current density at high magnetic fields in YBCO are the introduction of nanoparticles and chemical substitution of yttrium by other rare earth elements. Since low costs and environmental compatibility are essential conditions for the preparation of long length YBCO films, the cost effective chemical solution deposition (CSD) procedure was selected, given that no vacuum technology is required. To reveal the flexibility and the good optimization possibilities of the CSD approach two main processes were chosen for comparison: a fluorine-free method, namely the polymer-metal precursor technique, and a fluorine-based method, the metalorganic deposition (MOD) using the trifluoroacetates (TFA) technique. Sharp transition temperature widths ΔTc of 1.1 K for the polymer metal method, 0.8 K for TFA method and critical current densities Jc of ∼3.5 MA/cm2 shows that high quality YBCO thin films can be produced using both techniques. Especially interesting is the magnetic field dependence of the critical current density Jc(B) of the Y(Dy)BCO (80 %) films showing that for the lower magnetic fields the critical current density Jc(B) is higher for a standard YBCO film, but at fields higher than 4.5 T the critical current density Jc(B) of Y(Dy)BCO is larger than that for the YBCO. Above 8 T, Jc(B) of the Y(Dy)BCO film is more than one order of magnitude higher than in pure YBCO film. (orig.)

  14. Chemical and enzymatic preparation of acylglycerols containing C18 furanoid fatty acids.

    Science.gov (United States)

    Lie Ken Jie, M S; Syed-Rahmatullah, M S

    1995-01-01

    C18 furanoid triacylglycerol [glycerol tri-(9,12-epoxy-9,11-octadecadienoate)] was prepared by chemical transformation of triricinolein isolated from castor oil. The procedure involved oxidation, epoxidation and cyclization of the epoxy-keto intermediate with sodium azide and ammonium chloride in aqueous ethanol. The furanoid triacylglycerol was also obtained by esterification of C18 furanoid fatty acid with glycerol using Novozyme 435 (Novo Nordisk A.S., Bagsvaerd, Denmark) as biocatalyst. When Lipozyme (Novo Nordisk A.S.) was used, a mixture of the furanoid 1(3)-rac-monoacylglycerol and 1,3-diacylglycerol was obtained. In order to obtain the C18 furanoid 1,2(2,3)-diacylglycerol, selective hydrolysis of the furanoid triacylglycerol was achieved using porcine pancreatic lipase in tris(hydroxymethyl) methylamine buffer. Interesterification of triolein with methyl C18 furanoid ester in the presence of Lipozyme showed maximum incorporation of 34% of furanoid fatty acid. Extension of the interesterification to vegetable oils (olive, peanut, sunflower, corn and palm oil) allowed a maximum of 24% furanoid acid incorporation to be achieved. PMID:7760692

  15. Preparation and structure of porous dielectrics by plasma enhanced chemical vapor deposition

    International Nuclear Information System (INIS)

    The preparation of ultralow dielectric constant porous silicon, carbon, oxygen, hydrogen alloy dielectrics, called 'pSiCOH', using a production 200 mm plasma enhanced chemical vapor deposition tool and a thermal treatment is reported here. The effect of deposition temperature on the pSiCOH film is examined using Fourier transform infrared (FTIR) spectroscopy, dielectric constant (k), and film shrinkage measurements. For all deposition temperatures, carbon in the final porous film is shown to be predominantly Si-CH3 species, and lower k is shown to correlate with increased concentration of Si-CH3. NMR and FTIR spectroscopies clearly detect the loss of a removable, unstable, hydrocarbon (CHx) phase during the thermal treatment. Also detected are increased cross-linking of the Si-O skeleton, and concentration changes for three distinct structures of carbon. In the as deposited films, deposition temperature also affects the hydrocarbon (CHx) content and the presence of C=O and C=C functional groups

  16. Preparation and physico-chemical properties of hydrogels from carboxymethyl cassava starch crosslinked with citric acid

    Science.gov (United States)

    Boonkham, Sasikan; Sangseethong, Kunruedee; Chatakanon, Pathama; Niamnuy, Chalida; Nakasaki, Kiyohiko; Sriroth, Klanarong

    2014-06-01

    Recently, environmentally friendly hydrogels prepared from renewable bio-based resources have drawn significant attention from both industrial and academic sectors. In this study, chemically crosslinked hydrogels have been developed from cassava starch which is a bio-based polymer using a non-toxic citric acid as a crosslinking agent. Cassava starch was first modified by carboxymethylation to improve its water absorbency property. The carboxymethyl cassava starch (CMCS) obtained was then crosslinked with citric acid at different concentrations and reaction times. The gel fraction of hydrogels increased progressively with increasing citric acid concentration. Free swelling capacity of hydrogels in de-ionized water, saline solution and buffers at various pHs as well as absorption under load were investigated. The results revealed that swelling behavior and mechanical characteristic of hydrogels depended on the citric acid concentration used in reaction. Increasing citric acid concentration resulted in hydrogels with stronger network but lower swelling and absorption capacity. The cassava starch hydrogels developed were sensitive to ionic strength and pH of surrounding medium, showing much reduced swelling capacity in saline salt solution and acidic buffers.

  17. Ciprofloxacin adsorption from aqueous solution onto chemically prepared carbon from date palm leaflets

    Institute of Scientific and Technical Information of China (English)

    El-Said Ibrahim El-Shafey; Haider Al-Lawati; Asmaa Soliman Al-Sumri

    2012-01-01

    A chemically prepared carbon was synthesized from date palm leaflets via sulphuric acid carbonization at 160℃.Adsorption of ciprofloxacin (CIP) from aqueous solution was investigated in terms of time,pH,concentration,temperature and adsorbent status (wet and dry).The equilibrium time was found to be 48 hr.The adsorption rate was enhanced by raising the temperature for both adsorbents,with adsorption data fitting a pseudo second-order model well.The activation energy,Ea,was found to be 17 kJ/mol,indicating a diffusion-controlled,physical adsorption process.The maximum adsorption was found at initial pH 6.The wet adsorbent showed faster removal with higher uptake than the dry adsorbent,with increased performance as temperature increased (25-45℃ ).The equilibrium data were found to fit the Langmuir model better than the Freundlich model.The thermodynamic parameters showed that the adsorption process is spontaneous and endothermic.The adsorption mechanism is mainly related to cation exchange and hydrogen bonding.

  18. Preparation of Silicon Nanowire Field-effect Transistor for Chemical and Biosensing Applications.

    Science.gov (United States)

    Wu, Jennifer Yun-Shin; Lin, Chih-Heng; Feng, Mei-Huei; Chen, Chien-Hung; Su, Ping-Chia; Yang, Po-Wen; Zheng, Jian-Ming; Fu, Chang-Wei; Yang, Yuh-Shyong

    2016-01-01

    Surveillance using biomarkers is critical for the early detection, rapid intervention, and reduction in the incidence of diseases. In this study, we describe the preparation of polycrystalline silicon nanowire field-effect transistors (pSNWFETs) that serve as biosensing devices for biomarker detection. A protocol for chemical and biomolecular sensing by using pSNWFETs is presented. The pSNWFET device was demonstrated to be a promising transducer for real-time, label-free, and ultra-high-sensitivity biosensing applications. The source/drain channel conductivity of a pSNWFET is sensitive to changes in the environment around its silicon nanowire (SNW) surface. Thus, by immobilizing probes on the SNW surface, the pSNWFET can be used to detect various biotargets ranging from small molecules (dopamine) to macromolecules (DNA and proteins). Immobilizing a bioprobe on the SNW surface, which is a multistep procedure, is vital for determining the specificity of the biosensor. It is essential that every step of the immobilization procedure is correctly performed. We verified surface modifications by directly observing the shift in the electric properties of the pSNWFET following each modification step. Additionally, X-ray photoelectron spectroscopy was used to examine the surface composition following each modification. Finally, we demonstrated DNA sensing on the pSNWFET. This protocol provides step-by-step procedures for verifying bioprobe immobilization and subsequent DNA biosensing application. PMID:27167162

  19. Synthesis and optical properties of copper nanoparticles prepared by a chemical reduction method

    International Nuclear Information System (INIS)

    Copper nanoparticles, due to their interesting properties, low cost preparation and many potential applications in catalysis, cooling fluid or conductive inks, have attracted a lot of interest in recent years. In this study, copper nanoparticles were synthesized through the chemical reduction of copper sulfate with sodium borohydride in water without inert gas protection. In our synthesis route, ascorbic acid (natural vitamin C) was employed as a protective agent to prevent the nascent Cu nanoparticles from oxidation during the synthesis process and in storage. Polyethylene glycol (PEG) was added and worked both as a size controller and as a capping agent. Cu nanoparticles were characterized by Fourier transform infrared (FT-IR) spectroscopy to investigate the coordination between Cu nanoparticles and PEG. Transmission electron microscopy (TEM) and UV–vis spectrometry contributed to the analysis of size and optical properties of the nanoparticles, respectively. The average crystal sizes of the particles at room temperature were less than 10 nm. It was observed that the surface plasmon resonance phenomenon can be controlled during synthesis by varying the reaction time, pH, and relative ratio of copper sulfate to the surfactant. The surface plasmon resonance peak shifts from 561 to 572 nm, while the apparent color changes from red to black, which is partly related to the change in particle size. Upon oxidation, the color of the solution changes from red to violet and ultimately a blue solution appears

  20. Electrochromic properties of porous NiO thin films prepared by a chemical bath deposition

    Energy Technology Data Exchange (ETDEWEB)

    Xia, X.H.; Tu, J.P.; Zhang, J.; Wang, X.L. [Department of Materials Science and Engineering, Zhejiang University, Hangzhou 310027 (China); Zhang, W.K.; Huang, H. [College of Chemical Engineering and Materials Science, Zhejiang University of Technology, Hangzhou 310032 (China)

    2008-06-15

    Highly porous nickel oxide thin films were prepared on ITO glass by a simple chemical bath deposition (CBD) method in combination with a following heat-treatment process. XRD analysis revealed that the as-deposited precursor film contained {beta}-Ni(OH){sub 2} and {gamma}-NiOOH, and they changed to cubic polycrystalline NiO after annealing. The FTIR results showed presence of free hydroxyl ion and water in the NiO thin films. The electrochromic properties of NiO thin films were investigated in an aqueous alkaline electrolyte (1 M KOH) by means of transmittance, cyclic voltammetry (CV) and chronoamperometry (CA) measurements. The NiO thin film annealed at 300 C exhibited a noticeable electrochromism and good memory effect. The coloration efficiency was calculated to be 42 cm{sup 2} C{sup -1} at 550 nm, with a variation of transmittance up to 82%. The porous NiO thin films also showed good reaction kinetics with fast switching speed, and the coloration and bleaching time were 8 and 10 s, respectively. (author)

  1. Low-cost plasmonic solar cells prepared by chemical spray pyrolysis

    Directory of Open Access Journals (Sweden)

    Erki Kärber

    2014-12-01

    Full Text Available Solar cells consisting of an extremely thin In2S3/CuInS2 buffer/absorber layer uniformly covering planar ZnO were prepared entirely by chemical spray pyrolysis. Au nanoparticles (Au-NPs were formed via thermal decomposition of a gold(III chloride trihydrate (HAuCl4·3H2O precursor by spraying 2 mmol/L of the aqueous precursor solution onto a substrate held at 260 °C. Current–voltage scans and external quantum efficiency spectra were used to evaluate the solar cell performance. This work investigates the effect of the location of the Au-NP layer deposition (front side vs rear side in the solar cell and the effect of varying the volume (2.5–10 mL of the sprayed Au precursor solution. A 63% increase (from 4.6 to 7.5 mA/cm2 of the short-circuit current density was observed when 2.5 mL of the precursor solution was deposited onto the rear side of the solar cell.

  2. A new single buffer layer for YBCO coated conductors prepared by chemical solution deposition

    Energy Technology Data Exchange (ETDEWEB)

    Li Guo [Key Laboratory of Advanced Technologiesof Materials (Ministry of Education of China), Superconductivity R and D Center (SRDC), Mail Stop 165, Southwest Jiaotong University, Chengdu, Sichuan 610031 (China); Pu Minghua [Key Laboratory of Advanced Technologiesof Materials (Ministry of Education of China), Superconductivity R and D Center (SRDC), Mail Stop 165, Southwest Jiaotong University, Chengdu, Sichuan 610031 (China); Du Xiaohua [Key Laboratory of Advanced Technologiesof Materials (Ministry of Education of China), Superconductivity R and D Center (SRDC), Mail Stop 165, Southwest Jiaotong University, Chengdu, Sichuan 610031 (China); Zhang Yanbing [Key Laboratory of Advanced Technologiesof Materials (Ministry of Education of China), Superconductivity R and D Center (SRDC), Mail Stop 165, Southwest Jiaotong University, Chengdu, Sichuan 610031 (China); Zhou Huaming [Key Laboratory of Advanced Technologiesof Materials (Ministry of Education of China), Superconductivity R and D Center (SRDC), Mail Stop 165, Southwest Jiaotong University, Chengdu, Sichuan 610031 (China); Zhao Yong [Key Laboratory of Advanced Technologiesof Materials (Ministry of Education of China), Superconductivity R and D Center (SRDC), Mail Stop 165, Southwest Jiaotong University, Chengdu, Sichuan 610031 (China)]. E-mail: yzhao@home.swjtu.edu.cn

    2007-02-01

    A new single buffer layer YBiO{sub 3} has been proposed for YBCO coated conductors. Highly c-axis oriented YBiO{sub 3} buffer layer has been deposited on single crystal LaAlO{sub 3} by a low-cost chemical solution deposition method in a temperature range as low as 730-800 C in air. A very dense, smooth, pinhole-free morphology has been observed for YBiO{sub 3} buffer layer. Dense, homogeneous and epitaxially grown YBCO film has been obtained with its onset critical temperature 90 K and J {sub c} (77 K, 0 T) = 3.1 MA/cm{sup 2}. The addition of Bi{sub 2}O{sub 3}, which melts at around 817 C, has been argued to be responsible for the densification as well as low-process temperature of YBiO{sub 3} buffer layer. These results offer an alternative to prepare desirable buffer layer(s) for YBCO coated conductors via a cost-effective and easily scalable route.0.

  3. A new single buffer layer for YBCO coated conductors prepared by chemical solution deposition

    International Nuclear Information System (INIS)

    A new single buffer layer YBiO3 has been proposed for YBCO coated conductors. Highly c-axis oriented YBiO3 buffer layer has been deposited on single crystal LaAlO3 by a low-cost chemical solution deposition method in a temperature range as low as 730-800 C in air. A very dense, smooth, pinhole-free morphology has been observed for YBiO3 buffer layer. Dense, homogeneous and epitaxially grown YBCO film has been obtained with its onset critical temperature 90 K and J c (77 K, 0 T) = 3.1 MA/cm2. The addition of Bi2O3, which melts at around 817 C, has been argued to be responsible for the densification as well as low-process temperature of YBiO3 buffer layer. These results offer an alternative to prepare desirable buffer layer(s) for YBCO coated conductors via a cost-effective and easily scalable route

  4. A comparison of properties between carboxylated acrylic rubbers prepared by γ-ray irradiation and chemical method

    International Nuclear Information System (INIS)

    Acrylic rubbers (ACM) carboxylated by acrylic acid or itaconic acid were prepared by 60Co γ-ray or chemical-initiator (K2S2O8) induced emulsion copolymerization. The polymers were characterized by Fourier transform infrared spectroscopy (FT-IR). Acid value, molecular weight and polydispersity index (PDI) of the polymers were determined by non-aqueous titration method and gel permeation chromatography (GPC), respectively. Vulcanization and mechanical properties of the filled ACM were studied by rheometric measurement, gel fraction analysis, mechanical property tests and dynamic mechanical thermal analysis (DMTA). The results show that the ACMs prepared by γ-ray irradiation have lower acid value, higher molecular weight and narrower PDI than chemically prepared ACMs of the same compositions. The itaconic acid carboxylated ACM has better cure characteristics and mechanical properties than the acrylic acid carboxylated ACM. The itaconic acid carboxylated ACM prepared by γ-ray irradiation has higher gel fraction and better cure characteristics as well as mechanical properties than that prepared by chemical method. (authors)

  5. Preparation of highly porous carbonaceous sorbents from sewage sludge by physical and chemical activation

    Energy Technology Data Exchange (ETDEWEB)

    Ros, A.; Martin, M.J. [Girona Univ., Lab. d' Enginyerie Quimica i Ambiental, Dept. d' Enginyeria Quimica, Agraria i Tecnologia Agroalimentaria, Facultat de Ciencies (Spain); Lillo-Rodenas, M.A.; Linares-Solano, A. [Alicante Univ., Dept. de Quimica Inorganica (Spain); Fuente, E.; Montes-Moran, M.A. [Instituto Nacional del Carbon, CSIC, Oviedo (Spain)

    2005-07-01

    Among the different porous materials, activated carbon (AC) is the most widely used for environmental applications such as gas-phase pollutant removal, gas separation, solvent recovery and water purification, because of its high specific surfacea. Commercial activated carbons are generally produced from coals and lignocellulosic materials [1]. Additionally, in the latest years great attention is being focused on the reuse of wastes such as sewage sludges [2,3]. The objective of this study is to find more effective activating procedures to prepare AC from sewage sludge. Both dried sludges from two different WWTP (SL, SB) and their corresponding chars prepared by pyrolysis (SL-P, SB-P) were activated using physical activation (CO{sub 2}) and chemical activation (H{sub 3}PO{sub 4}, NaOH and KOH). As shown in Table 1, pyrolysis of the raw sludges slightly increased the specific surface area, up to 50 m{sup 2}/g. Acid-washing of the pyrolyzed samples with 5 M HCl removes part of the metal content leading to an increase in the specific surface areas for both SL-PD and SB-PD, with surface areas of 428 m{sup 2}/g and 188 m{sup 2}/g, respectively. This simple washing treatment is useful for the development of porous adsorbents, especially in the case of SL derived materials. Our results show that CO{sub 2} physical activation of the pyrolyzed and the HCl-washed samples develops no appreciable porosity in the final materials, under the experimental conditions used. For CO{sub 2} activation, maximum temperatures of 870 C and holding times up to 4 hours in CO{sub 2} (100 ml/min) were used. Chemical activation with H{sub 3}PO{sub 4} of the pristine samples and those pyrolyzed was performed at 450 C, a temperature typically used for the activation by H{sub 3}PO{sub 4} of lignocellulosic precursors, and using two different H{sub 3}PO{sub 4} solutions (30 and 50% wt). These conditions were not either suitable for an efficient porosity development. A detailed study about the

  6. NOVEL PREPARATION AND MAGNETO CHEMICAL CHARACTERIZATION OF NANOPARTICLE MIXED ALCOHOL CATALYSTS

    Energy Technology Data Exchange (ETDEWEB)

    Seetala V. Naidu; Upali Siriwardane

    2005-05-24

    We have developed and streamlined the experimental systems: (a) Laser-induced solution deposition (LISD) photosynthesis, ball-milling, and chemical synthesis of Fe, Co, and Cu nanoparticle catalysts; (b) Sol-gel method for mesoporous {gamma}-Al{sub 2}O{sub 3}, SiO{sub 2}, hybrid alumina/silica granular supports; (c) Three sol-gel/oil-drop catalyst preparation methods to incorporate metal nanoparticles into mesoporous 1 mm granular supports; (d) Low-cost GC-TCD system with hydrogen as carrier gas for the determination of wide spectrum of alkanes produced during the F-T reactions; and (e) Gas-flow reactor and microchannel reactor for fast screening of catalysts. The LISD method could produce Co, Cu, and Fe (5 nm) nanoparticles, but in milligram quantities. We could produce nanoparticles in gram quantities using high-energy ball milling and chemical synthesis methods. Ball milling gave wide particle size distribution compared to the chemical synthesis method that gave almost uniform size ({approx}5 nm) particles. Metal nanoparticles Cu, Co, Fe, Cu/Co, Cu/Fe and Co/Fe were loaded (2-12 wt%) uniformly into {gamma}-Al{sub 2}O{sub 3}, SiO{sub 2}, or alumina/silica hybrid supports by combined sol-gel/oil-drop methods followed by calcination and hydrogenation steps, prior to syngas FT reaction studies. The properties of metal loaded {gamma}-Al{sub 2}O{sub 3} granules were compared for the two precursors: aluminum tri-sec-butoxide (ALTSB) and aluminum tri-iso-propoxide (ALTIP). The effect of solgel supports alumina, silica, and alumina/silica hybrid were examined on catalytic properties. Metal loading efficiencies for pure metal catalysts increased in the order Co, Cu and Fe in agreement with solubility of metal hydroxides. In case of mixed metals, Co and Cu seams to interfere and reduce Fe metal loading when metal nitrate solutions are used. The solubility differences of metal hydroxides would not allow precise control of metal loading. We have overcome this problem by

  7. High coercivity Gd-substituted Ba hexaferrites, prepared by chemical coprecipitation

    Science.gov (United States)

    Litsardakis, G.; Manolakis, I.; Serletis, C.; Efthimiadis, K. G.

    2008-04-01

    A series of Gd-substituted Ba hexaferrites with nominal formula (Ba1-xGdx)Oṡ5.25 Fe2O3 (x=0-0.30) were prepared by the chemical coprecipitation method from nitrate precursors and heating at T =800-1200°C for 2h. The samples have been examined by x-ray diffraction, vibrating-sample magnetometer, and scanning electron microscopy methods. Gd substituted samples form single phase materials with the M-type hexaferrite structure at all heating temperatures, in the range of x ⩽0.10-0.20. The saturation magnetization (at 1.8T) varies slightly with x in most cases and, for x =0.05-0.10, it increases up to 66.7Am2/kg, exceeding the value of the unsubstituted hexaferrite. A strong enhancement of the coercivity is observed for all substituted samples, with maximum values Hc=457kA/m for the single-phase x =0.10 sample annealed at 1000°C and Hc=477kA/m for the x =0.25 sample annealed at 1100°C which contains Fe2O3 and GdFeO3 impurities. As the variation of coercivity with either substitution rate (x ) or annealing temperature is not monotonic, three different factors may account for the high coercivities that are obtained: (a) an inhibition of grain growth due to the presence of Gd, (b) a possible inherent effect on magnetocrystalline anisotropy, especially for single phase samples, and (c) a microstructural effect of secondary phases.

  8. Extended phase homogeneity and electrical properties of barium calcium titanate prepared by the wet chemical methods

    International Nuclear Information System (INIS)

    Ca-substituted BaTiO3 with extended homogeneity range upto ∼50 mol% CaTiO3 have been prepared by three different chemical routes namely carbonate-oxalate (COBCT), gel-carbonate (GCBCT), and gel-to-crystallite conversion (GHBCT) followed by heat treatment above 1150 deg. C. X-ray powder diffraction (XRD) data show continuous decrease in the tetragonal unit cell parameters as well as c0/a0 ratio with CaTiO3 content, which are in accordance with the substitution of smaller sized Ca2+ ions at the barium sites. The microstructure as well as the dielectric properties are greatly influenced by the cationic ratio, α=(Ba+Ca)/Ti. The grain size decreases with CaTiO3 content for the stoichiometric samples (α=1), whereas ultrafine microstructure is observed in the case of off-stoichiometric samples (α>1) for the whole compositional range of CaTiO3 concentrations. Sharper εr-T characteristics at lower calcium content and broader εr-T with decreased εmax, in the higher calcium range are observed in the case of α=1. Whereas nanometer grained ceramics exhibiting diffuse εr-T characteristics are obtained in the case of α>1. The positive temperature coefficient of resistivity (PTCR) is realized for barium calcium titanate ceramics having 0.3 at.% Sb as the donor dopant for higher CaTiO3 (typically 30 mol%) containing samples (α=1), indicating that Ca2+ ions do not behave as acceptors if they were to substitute at the Ti4+ sites. Whereas the off-stoichiometric (α>1) ceramics retained high resistivity, indicative of the Ti-site occupancy for Ca2+ in fine grain ceramics

  9. Chemical synthesis of 5-azacytidine nucleotides and preparation of tRNAs containing 5-azacytidine in its 3'-terminus.

    OpenAIRE

    Zielinski, W S; Sprinzl, M.

    1984-01-01

    5-azacytidine-5'-triphosphate prepared from 5-azacytidine by chemical phosphorylation is a substrate for AMP (CMP) tRNA nucleotidyl transferase from yeast. tRNAsPhe from yeast containing 5-azacytidine in their 3'-termini were prepared enzymatically. tRNAPhe-Cpn5CpA and tRNAPhe-n5Cpn5CpA can be aminoacylated by phenylalanyl-tRNA synthetase from yeast and they are active in the poly(U)-dependent synthesis of poly(Phe) on E. coli ribosomes. The decomposition of 5-azacytidine via hydrolysis of th...

  10. Studies on Physico-Chemical Properties of Noni Fruit (Morinda Citrifolia ) and Preparation of Noni Beverages

    OpenAIRE

    Joshi, A. A.; Chilkawar P.M; Jadhav B.A

    2012-01-01

    Noni (Morinda citrifolia linn) fruits are edible but they don’t have nice taste and flavor. In present investigation attempts have been made to standardize the recipes for preparation of noni beverages i.e. RTS, Squash and Syrup and to study the physicochemical characteristics of noni fruit and techno economic feasibility of prepared beverages. The recipe for preparation of Noni RTS beverage was standardized by varying the levels of juice, TSS. Study revealed that the final b...

  11. CHEMICAL ANALYSIS OF NIRGUNDI TAILA WITH SPECIAL REFERENCE TO PREPARATION IN DIFFERENT NUMBER OF DAYS

    OpenAIRE

    Prashanth B K; Rao K Shankar; Krishnamurthy M.S; Rao Ravi; Bhat Smitha

    2012-01-01

    Sneha kalpana is a process where the active principles present in the drug are extracted with the Sneha (Ghee or Oil) during the pharmaceutical process. The method of preparation of different Taila kalpanas requires different Drava dravyas and different number of days for the paka. Nirgundi taila as said in Charaka Samhita Chikitsa sthana 28/134 was prepared with Tila taila as the base. The three different oil samples were prepared by adding Nirgundi Patra Swarasa as the drava dravya. The sam...

  12. Chemical and immunological characteristics of four different L-asparaginase preparations.

    Science.gov (United States)

    Koerholz, D; Brueck, M; Nuernberger, W; Juergens, H; Goebel, U; Wahn, V

    1989-05-01

    We studied the differences in protein composition and immunologic reactivity of two E. coli-derived L-asparaginase (l-Asp) preparations (I and II), Erwinia-Asp (III) and PEG-modified E. coli l-Asp (IV). On gel filtration, each of preparations I-III showed three major peaks at 100, 270 and 460 KD, all with enzyme activity, whereas PEG-Asp showed peaks at 35 and 220 KD. On SDS-PAGE one major subunit could be identified at 32 KD (I and II) or 40 KD (III), whereas PEG-modified l-Asp could only be detected by lowering the polyacrylamide concentration and gave a single band above 200 KD. Using a polyclonal rabbit antibody generated against preparation I, only the E. coli l-Asp preparations (I and II) formed precipitin lines on Ouchterlony double diffusion. After freezing and thawing, preparation IV also reacted with this antibody. In sera from patients treated with preparation I, antibodies (detected by ELISA) reacted with preparations I and II but not with preparations III and IV. These results indicate that Erwinia-Asp (III) and PEG-Asp (IV) are distinct from E. coli preparations (I and II) by molecular weight and immunological behavior. They also provide an experimental rationale for the use of Erwinia-Asp as well as PEG-Asp in E. coli Asp-sensitized patients. PMID:2659379

  13. Effects of Heating Processing on Microstructure and Magnetic Properties of Mn-Zn Ferrites Prepared via Chemical Co-precipitation

    Institute of Scientific and Technical Information of China (English)

    CHEN Shijie; XIA Jingbing; DAI Jianqing

    2015-01-01

    The fine powders of Mn-Zn ferrites with uniform size were prepared via chemical co-precipitation method. X-ray diffraction analysis (XRD), scanning electron microscopy (SEM), vibrating sample magnetometer (VSM), frequency dependence of permeability and metallographical microscope were used to investigate the crystal structure, surface topography and magnetic properties of the powders and the sintering samples. The experimental results demonstrate that the precursor powders have formed a pure phase cubic spinel MnxZn1-xFe2O4 while in the reactor and show deifnite magnetism, which can solve the dififcult issue in washing process effectively. When calcined beneath 450℃, the powders have intact crystal form and the crystallite size is less than 20 nm. Comparison tests of sintering temperatures show that 1 300℃ is the ideal sintering temperature for Mn-Zn ferrites prepared by using the chemical co-precipitation.

  14. A New Chemical Method of Preparing Semiconducting MoX2 (X=S, Se) Thin Films

    Science.gov (United States)

    Mandal, Krishna Chandra; Savadogo, Oumarou

    1991-12-01

    We report a new chemical method for preparing semiconducting MoX2 (X=S, Se) thin films on glass substrates. For MoS2 deposition, an ammine complex of Mo (VI) ions, thioacetamide and hydrazine hydrate solutions was used, while for MoSe2 films, sodium selenosulphate solution replaced thioacetamide, and other reagents remained unchanged. Structural, optical and electrical properties of the as-deposited and annealed films have been studied.

  15. Antimicrobial activity of novel nanostructured Cu-SiO2 coatings prepared by chemical vapour deposition against hospital related pathogens

    OpenAIRE

    Varghese, Sajnu; ElFakhri, Souad O; Sheel, David W.; Sheel, Paul; Bolton, Frederick J Eric; Foster, Howard A

    2013-01-01

    There is increasing recognition that the healthcare environment acts as an important reservoir for transmission of healthcare acquired infections (HCAI). One method of reducing environmental contamination would be use of antimicrobial materials. The antimicrobial activity of thin silica-copper films prepared by chemical vapour deposition was evaluated against standard strains of bacteria used for disinfectant testing and bacteria of current interest in HCAI. The structure of the coatings was ...

  16. Chemical and structural evaluation of activated carbon prepared from jute sticks for Brilliant Green dye removal from aqueous solution.

    Science.gov (United States)

    Asadullah, Mohammad; Asaduzzaman, Mohammad; Kabir, Mohammad Shajahan; Mostofa, Mohammad Golam; Miyazawa, Tomohisa

    2010-02-15

    Activated carbons have been prepared from jute sticks by chemical activation using ZnCl(2) and physical activation using steam for the removal of Brilliant Green dye from aqueous solution. The activated carbons and charcoal prepared from jute sticks were characterized by evaluating the surface chemistry, structural features and surface morphology. The maximum BET surface area was obtained to be 2304 m(2)/g for chemical activated carbon (ACC) while it is 730 and 80 m(2)/g for steam activated carbon (ACS) and charcoal, respectively. The FT-IR spectra exhibited that the pyrolysis and steam activation of jute sticks resulted in the release of aliphatic and O-containing functional groups by thermal effect. However, the release of functional groups is the effect of chemical reaction in the ZnCl(2) activation process. A honeycomb-type carbon structure in ACC was formed as observed on SEM images. Although charcoal and ACC were prepared at 500 degrees C the ACC exhibited much lower Raman sensitivity due to the formation of condensed aromatic ring systems. Due to high surface area and high porous structure with abundance of functional groups, the ACC adsorbed dye molecules with much higher efficiency than those of ACS and charcoal. PMID:19815339

  17. New low temperature methods for the preparation of pure and chemically substituted derivatives of Ba2YCu4O8

    International Nuclear Information System (INIS)

    Samples of single phase 124 have been prepared at temperatures below 775C under 1 atm of O2 using freeze-dried nitrates and metal organic precursors. Below 700C the stable phase assemblage is Ba2Cu3O6-x + CuO + Y2O3. 124 samples formed by these methods have particle sizes as low as 0.3 μ, and are ideally suited for thick film preparation. In an attempt to increase the stability of this phase, the authors have also prepared various chemically substituted derivatives; including Ca for Y, which is known to increase Tc, and Ba for Sr. These results together with the properties of 124 thick films will be discussed

  18. Study on Physical and Chemical Behaviors of Rare Earths in Preparing Ceramic Tube Supported Palladium Film by Electroless Plating

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    The rare earths of ytterbium, lanthanum, praseodymium, neodymium and their binary mixtures were respectively added into the traditional electroless plating solution to prepare thin palladium film on the inner surface of porous ceramic tube. The experimental results shows that the addition of rare earths increases palladium deposition rates and the binary mixtures are superior to the single rare earths and the mixture of ytterbium-lanthanum is the most efficient. Adding the mixture of ytterbium-lanthanum can also reduce the plating temperature by 10~20 ℃, shrink the metal crystal size and improve the film densification compared to those by traditional electroless plating. A thin palladium film with 5 μm was prepared and the film made a highly pure hydrogen with a molar fraction of more than 99.97% from a H2-N2 gas mixture. More attentions were paid to analyze the physical and chemical behaviors of the rare earths in palladium film preparation.

  19. Characterizations on the microstructures of LiMn2O4 prepared by a simple soft-chemical technique

    International Nuclear Information System (INIS)

    LiMn2O4 powders were prepared by a simple soft-chemical technique at different temperatures. X-ray diffraction and thermogravimetric analysis suggested that the material prepared at 800 deg. C was stoichiometric LiMn2O4, whereas those prepared at 600 and 700 deg. C were Li[Mn0.773+Mn1.234+]O4.115 and Li[Mn0.853+Mn1.154+]O4.075. Several typical XRD peaks of the compounds were investigated with an aim to elucidate (i) the Li immigration to the 16d octahedral sites, (ii) the partial tetragonal phase transition of the material and (iii) the mean coherent domain size and microstrain. SEM study showed that the particle size of the materials increased with heating temperature. The activation energy for the material particle growth was determined as 30.4 kJ mol-1

  20. A chemical deposition method to prepare circular planar 147Pm sources for the measurement of particulate emission in air

    International Nuclear Information System (INIS)

    This paper describes a method for preparing a circular planar source of 17 mm diameter containing approximately 400 kBq of 147Pm employing a wet chemical deposition technique to be used in dust monitors. This manuscript described the overall process concept and experimental procedure. The technical feasibility, efficiency of the process and product quality has been evaluated. The quality of the prepared source in terms of nonleachability, uniform distribution of activity and stability, which are necessary attributes of a radioactive source were evaluated and found to be satisfactory. - Highlights: • Preparation of circular planar 147Pm source for dust monitors. • Evaluation of efficiency of the process and product quality. • Quality evaluation of the sources

  1. Magnetic properties of lanthanum orthoferrite fine powders prepared by different chemical routes

    Indian Academy of Sciences (India)

    Benedict Ita; P Murugavel; V Ponnambalam; A R Raju

    2003-10-01

    Fine powders of lanthanum iron oxide, LaFeO3, have been prepared by solid state reaction as well as sol-gel synthesis and nebulized spray pyrolysis. Structures, morphologies and magnetic susceptibility measurements of these powders have been examined. The powders prepared by all the three low-temperature routes contain nearly spherical particles with an average diameter of 40 nm. These samples show a lower Neel temperature than the powder prepared by solid state reaction besides showing much lower magnetic susceptibility at low temperatures.

  2. 78 FR 4446 - Exempt Chemical Preparations Under the Controlled Substances Act

    Science.gov (United States)

    2013-01-22

    ... and dependence and are controlled to protect the public health and safety. Section 201 of the CSA (21...... Flurazepam ....... Vial: 1 mL 12/22/2011 American Radiolabeled Chemicals, Inc... Heroin (1 mg/mL) Vial: 1 mL 12/22/2011 American Radiolabeled Chemicals, Inc... Heroin Vial: 1 mL 12/22/2011 American...

  3. Final status report in preparation for the chemical cleaning of Dresden-1, DNS-D1-034

    International Nuclear Information System (INIS)

    This report discusses the status of all of the activities conducted in preparation for the chemical cleaning of the Dresden-1 Nuclear Power Plant of Commonwealth Edison of Illinois. The metallurgical testing of a solvent and its ability to remove radioactivity are reviewed. Included are all engineering details relating to the modifications to the primary system to be able to perform the chemical cleaning and to rinse the cleaning solvent out of the equipment. A facility to store and process spent cleaning solutions is described in detail. Construction activities and preoperational activities are recounted. Licensing activities, quality assurance, safety, and radiation protection are discussed. The report includes recommendations for future actions for restarting the project when approval is received. All of the efforts discussed in this Final Status Report led to the conclusion that the chemical cleaning, as planned, was feasible. All of the necessary modifications and new equipment are in place and are operational

  4. Preparation of technetium-99-DMS renal complex in solution and its chemical and biological characterization

    International Nuclear Information System (INIS)

    99Tc-DMS solution was prepared by double isotope labelling, purified by molecular sieving through Sepharose 2B column, and checked by chromatographic and spectrophotometric methods, as well as by assessment of its biodistribution in rats. The preparations, obtained in a series of nine experiments, showed high renal uptake (30-40% of injected dose per organ) and could be used for further investigations of Tc-DMS biochemical behaviour in kidney tissue at subcellular level. Radioactive concentrations of purified 99Tc-DMS preparations were 37-74 Bq/ml and absorption maxima at 412-425 nm (yellow complex). By application of sup(99m)Tc, 99Tc-DMS preparation in rats, good renal scans have been obtained. (author)

  5. XMCD studies of Co{sub x}Pt{sub 100-x} nanoparticles prepared by vapour deposition and chemical synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Imperia, P. [Universitaet Hamburg, Institut fuer Experimentalphysik, Luruper Chaussee 149, 22761 Hamburg (Germany); ANSTO, Institute of Materials and Engineering, New Illawarra Road, Lucas Heights, Sydney, NSW (Australia); Glaser, L.; Martins, M.; Wurth, W. [Universitaet Hamburg, Institut fuer Experimentalphysik, Luruper Chaussee 149, 22761 Hamburg (Germany); Andreazza, P.; Penuelas, J.; Andreazza-Vignolle, C. [Centre de Recherce sur la Matiere Divisee, UMR6619, CNRS-University of Orleans, 1B rue de la Ferollerie, 45071 Orleans Cedex 2 (France); Alessandrovic, V.; Weller, H. [Universitaet Hamburg, Institut fuer Physikalische Chemie, Grindelallee 117, 20146 Hamburg (Germany)

    2008-05-15

    An almost linear relation between the Pt amount and the orbital to spin moment ratio ({mu}{sub l}/{mu}{sub s}) has been found in Co{sub x}Pt{sub 100-x} nanoparticles prepared by vapour deposition and possessing a well defined chemically disordered crystallographic structure. X-ray magnetic circular dichroism (XMCD) measurements done at the L{sub 2,3}Co edges show that a 4.0 nm, x=100 Co reference sample has a ratio {mu}{sub l}/{mu}{sub s}=0.097, comparable to values found for Co thin layers. An increase of the amount of Pt increases the {mu}{sub l}/{mu}{sub s} value: {mu}{sub l}/{mu}{sub s}=0.11 for x=78, {mu}{sub l}/{mu}{sub s}=0.12 when x=74 and finally, for x=38 it becomes {mu}{sub l}/{mu}{sub s}=0.140. Nanoparticles prepared by chemical synthesis with size proportional to changes of the stoichiometric ratio, from Co{sub 25}Pt{sub 75} to Co{sub 50}Pt{sub 50}, show values of the orbital to spin moment ratio compatible with the trend found for the former ones. The samples prepared by chemical synthesis in a diameter range from 4 nm to 8 nm are characterized by a sharp size distribution of 10%. In contrast to the in situ prepared nanoparticles that are oxide free, however, they show a varying degree of surface oxidation depending on the ambient conditions they are exposed to. (copyright 2008 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  6. Growth and properties of few-layer graphene prepared by chemical vapor deposition

    OpenAIRE

    Park, Hye Jin; Meyer, Jannik; Roth, Siegmar; Skakalova, Viera

    2009-01-01

    The structure, and electrical, mechanical and optical properties of few-layer graphene (FLG) synthesized by chemical vapor deposition (CVD) on a Ni coated substrate were studied. Atomic resolution transmission electron microscope (TEM) images show highly crystalline single layer parts of the sample changing to multilayer domains where crystal boundaries are connected by chemical bonds. This suggests two different growth mechanisms. CVD and carbon segregation participate in the growth process ...

  7. Magnetically assisted chemical separation (MACS) process: Preparation and optimization of particles for removal of transuranic elements

    International Nuclear Information System (INIS)

    The Magnetically Assisted Chemical Separation (MACS) process combines the selectivity afforded by solvent extractants with magnetic separation by using specially coated magnetic particles to provide a more efficient chemical separation of transuranic (TRU) elements, other radionuclides, and heavy metals from waste streams. Development of the MACS process uses chemical and physical techniques to elucidate the properties of particle coatings and the extent of radiolytic and chemical damage to the particles, and to optimize the stages of loading, extraction, and particle regeneration. This report describes the development of a separation process for TRU elements from various high-level waste streams. Polymer-coated ferromagnetic particles with an adsorbed layer of octyl(phenyl)-N,N-diisobutylcarbamoylmethylphosphine oxide (CMPO) diluted with tributyl phosphate (TBP) were evaluated for use in the separation and recovery of americium and plutonium from nuclear waste solutions. Due to their chemical nature, these extractants selectively complex americium and plutonium contaminants onto the particles, which can then be recovered from the solution by using a magnet. The partition coefficients were larger than those expected based on liquid[liquid extractions, and the extraction proceeded with rapid kinetics. Extractants were stripped from the particles with alcohols and 400-fold volume reductions were achieved. Particles were more sensitive to acid hydrolysis than to radiolysis. Overall, the optimization of a suitable NMCS particle for TRU separation was achieved under simulant conditions, and a MACS unit is currently being designed for an in-lab demonstration

  8. Solidification of regeneration solutions of filters for chemical water purification and coagulation pulps of water preparation

    International Nuclear Information System (INIS)

    The basic technical solutions, related to solidification of dangerous liquid industrial wastes, are presented. The method, mostly safe by the total discharge of dangerous substances into the environmental medium, is selected. Such a method envisages slagging of water preparation wastes with mixed activation (%5 CaO + 5% NaOH of the slag mass)

  9. Preparation of low-resistivity n-type ZnSe by organometallic chemical vapor deposition

    Science.gov (United States)

    Stutius, W.

    1981-03-01

    Low-resistivity n-type ZnSe with pTriethylaluminum is used as a dopant. The as-grown layers show a strong near-band-gap photoluminescence peak. The much weaker photoluminescence intensity at longer wavelength indicates that the concentration of deep centers is lower than in doped ZnSe prepared by other methods.

  10. Hydrogenation of Furfural to Furfuryl Alcohol over Co-B Amorphous Catalysts Prepared by Chemical Reduction in Variable Media

    Institute of Scientific and Technical Information of China (English)

    LI, Hui; CHAI, Wei-Mei; LUO, Hong-Shan; LI, He-Xing

    2006-01-01

    Five Co-B amorphous alloy catalysts were prepared by chemical reduction in different media, including pure water and pure ethanol as well as the mixture of ethanol and water with variable ethanol content. Their catalytic properties were evaluated using liquid phase furfural hydrogenation to furfuryl alcohol as the probe reaction. It was found that the reaction media had no significant influence on either the amorphous structure of the Co-B catalyst or the electronic interaction between metallic Co and alloying B. This could successfully account for the fact that all the as-prepared Co-B catalysts exhibited almost the same selectivity to furfuryl alcohol and the same activity per surface area ( RSH ), which could be considered as the intrinsic activity, since the nature of active sites remained unchanged. However, the activity per gram of Co ( RmH ) of the as-prepared Co-B catalysts increased rapidly when the ethanol content in the water-ethanol mixture used as the reaction medium for catalyst preparation increased. This could be attributed to the rapid increase in the surface area possibly owing to the presence of more oxidized boron species which could serve as a support for dispersing the Co-B amorphous alloy particles.

  11. The preparation of low electroendosmosis agarose and its physico-chemical property

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Studies on Gelidium amansii agar fractionations were carried out in this paper. Gelidium amansii agar was fractionated on DEAE-Cellulose, and four fractions were obtained sequentially. The fractions were analyzed on physical and chemical properties, and IR and 13C-NMR spectroscopy applied for elucidating the chemical structure. Among the four fractions obtained, water fraction measured up to the standard of low EEO agarose. The sulfate content, ash content, electroendosmosis and gel strength(1%) of water fraction were 0.16%, 0.34%, 0.12 and 1 130g/cm2 respectively, similar to those of the Sigma products.

  12. Morphology of carbon nanotubes prepared via chemical vapour deposition technique using acetylene: A small angle neutron scattering investigation

    Indian Academy of Sciences (India)

    D Sen; K Dasgupta; J Bahadur; S Mazumder; D Sathiyamoorthy

    2008-11-01

    Small angle neutron scattering (SANS) has been utilized to study the morphology of the multi-walled carbon nanotubes prepared by chemical vapour deposition of acetylene. The effects of various synthesis parameters like temperature, catalyst concentration and catalyst support on the size distribution of the nanotubes are investigated. Distribution of nanotube radii in two length scales has been observed. The number density of the smaller diameter tubes was found more in number compared to the bigger one for all the cases studied. No prominent scaling of the structure factor was observed for the different synthesis conditions.

  13. Preparation of Nano-Particles (Pb,La)TiO3 Thin Films by Liquid Source Misted Chemical Deposition

    Institute of Scientific and Technical Information of China (English)

    张之圣; 曾建平; 李小图

    2004-01-01

    Nano-particles lanthanum-modified lead titanate (PLT) thin films are grown on Pt/Ti/SiO2/Si substrate by liquid source misted chemical deposition (LSMCD). PLT films are deposited for 4-8 times, and then annealed at various temperature. XRD and SEM show that the prepared films have good crystallization behavior and perovskite structure. The crystallite is about 60 nm. The deposition speed is 3 nm/min. This deposition method can exactly control stoichiometry ratios, doping concentration ratio and thickness of PLT thin films. The best annealing process is to bake at 300 ℃ for 10 min and anneal at 600 ℃ for 1 h.

  14. Application of phase equilibria and chemical thermodynamics to the preparation, farbiration, and performance of advanced fast reactor fuel materials

    International Nuclear Information System (INIS)

    Described are some phase equilibria and chemical thermodynamics of systems relevant to the production and operation of the so-called ''advanced'' fast breeder reactor fuels. The systems discussed include UPu carbides, nitrides, oxycarbides and carbonitrides. Some examples of the application of these phase equilibria to the preparation, fabrication and behaviour of the materials in temperature gradients appropriate to reactor conditions are presented. Finally, aspects of the complex four and five component, U-C-O-N and U-Pu-C-O-N systems are discussed, a detailed knowledge of which is required for an analysis of advanced fuel behaviour

  15. Chemical modifiers in electrothermal atomic absorption determination of Platinum and Palladium containing preparations in blood serum

    Directory of Open Access Journals (Sweden)

    Аntonina Alemasova

    2012-11-01

    Full Text Available The biological liquids matrixes influence on the characteristic masses and repeatability of Pt and Pd electrothermal atomic absorption spectroscopy (ETAAS determination was studied. The chemical modifiers dimethylglyoxime and ascorbic acid for matrix interferences elimination and ETAAS results repeatability improvement were proposed while bioliquids ETAAS analysis, and their action mechanism was discussed.

  16. Preparation of 99Mo from the 100Mo(γ,n) reaction and chemical separation of 99mTc

    International Nuclear Information System (INIS)

    The radionuclide 99Mo has been prepared by 100Mo(γ, n) reaction using two types of natural molybdenum compound (molybdenum trioxide and zirconium molybdate gel) with the bremsstrahlung end-point energies of 10 and 15 MeV. After the equilibrium, 99mTc was separated as NaTcO4 from the irradiated samples using two different chemical procedures to examine the chemical yield. The separated Na[99mTc]TcO4 from the ZrMo gel has the 99Mo breakthrough of <10-4 %, radiochemical purity >99 % as well as chemical impurities of Al, Mo and Zr < 10 ppm. The estimation of 99Mo and 99mTc was done by using off-line c-ray spectrometric technique. The chemical yield of the separated 99mTc from the dissolved molybdenum trioxide is 70.7-75.2 %, whereas in the undissolved zirconium molybdate gel, it is 19.1-43 %. The second method is preferable because it is user friendly in hospital radiopharmacy throughout the shelf-life. (author)

  17. Error sensitivity to environmental noise in quantum circuits for chemical state preparation

    CERN Document Server

    Sawaya, Nicolas P D; McClean, Jarrod R; Aspuru-Guzik, Alán

    2016-01-01

    Calculating molecular energies is likely to be one of the first useful applications to achieve quantum supremacy, performing faster on a quantum than a classical computer. However, if future quantum devices are to produce accurate calculations, errors due to environmental noise and algorithmic approximations need to be characterized and reduced. In this study, we use the high performance qHiPSTER software to investigate the effects of environmental noise on the preparation of quantum chemistry states. We simulate nineteen 16-qubit quantum circuits under environmental noise, each corresponding to a unitary coupled cluster state preparation of a different molecule or molecular configuration. Additionally, we analyze the nature of simple gate errors in noise-free circuits of up to 40 qubits. We find that the Jordan-Wigner (JW) encoding produces consistently smaller errors under a noisy environment as compared to the Bravyi-Kitaev (BK) encoding. For the JW encoding, pure-dephasing noise is shown to produce substa...

  18. Chemical compositions of spherical titanium powders prepared by RF induction plasma

    International Nuclear Information System (INIS)

    Spherical titanium powders were prepared by RF induction plasma technology. The particle size is essentially un- changed, while the particle size distribution is relatively narrow after spheroidization processing. X-ray diffraction (XRD) random testing of the spherical titanium powders shows no structure and phase changes. The content of O, H, N and C decreases, while the content of Ti increases slightly. It indicates that spheroidization with RF plasma can enhance powder purity. (authors)

  19. Preparation of ZnO nanoparticles showing upconversion luminescence through simple chemical method

    Science.gov (United States)

    Anjana, R.; Subha, P. P.; Markose, Kurias K.; Jayaraj, M. K.

    2016-05-01

    Upconversion luminescence is an interesting area while considering its applications in a vast variety of fields. Rare earth ions like erbium is the most studied and efficient candidate for achieving upconversion. Erbium and ytterbium co-doped ZnO nanoparticles were prepared through co-precipitation method. A strong red emission has been obtained while exciting with 980 nm laser. Dependence of luminescence emission colour on ytterbium concentration has been studied.

  20. Some physico-chemical and radiation properties of plutonium-238 metal prepared by electrochemical amalgamation

    International Nuclear Information System (INIS)

    Pu-238 metal was prepared by electrolytic amalgamation from Pu(III) acetate aqueous solution and by followed by the thermal decomposition of the Pu amalgam. The density, specific heat power, γ-spectra, neutron flux, and corrosion kinetics in dry air at ambient temperature of the prepared 238Pu metal were measured. The neutron flux and γ-spectra from 238Pu metal have been attributed to spontaneous and induced fission and to (α,α'γ), (α,pγ), and (α,nγ) nuclear reactions on light nuclei. The electrochemically prepared 238Pu metal was shown to generate fewer neutrons, produce less gamma radiation, and contains lower 10B, 19F, and 28Si impurities in comparison with biomedical 238PuO2. The increase of neutron flux from the sample due to the reaction 18O(α,nγ) 21Ne was shown to be proportional to the increase of the mass of the 238Pu metal with time due to corrosion in dry air. 238Pu metal corrosion rate maximum and average values (1.1 x 10-2 and 4.7 x 10-3 mg cm-2 h-1, respectively) obtained in dry air were an order of magnitude higher than the rates published for 239Pu under similar experiment conditions. The difference between the 239Pu and 238Pu metal corrosion rate and mechanism is proposed to be due to the greater radiation effects and temperature on the 238Pu surface

  1. Preparation and characterization of copper indium disulfide films by facile chemical method

    International Nuclear Information System (INIS)

    A convenient and low cost technology was employed to prepare copper indium disulfide thin films, which can be analogous to other chalcogenides. The designed precursor solutions with Cu/In ratio at 1.5:1, 1:1, and 1:1.5, respectively, were prepared and coated on the glass substrate by dip-withdrawing method. The thin films were characterized by XRD, SEM, UV-Vis-NIR spectrophotometer, NKD-7000W spectrophotometer, Raman microscope and wavelength dispersive XRF spectrometer. As a result, chalcopyrite-type CuInS2 is the dominant phase in final products. Cu xS is also obtained as a minor phase composition. The as-prepared CuInS2 films are of high absorption coefficient of 2.65 x 105 cm-1 at 400 nm and 1.7 x 105 cm-1 at 600 nm. The calculated band gap values are 1.28-1.62 eV, according with the theoretical band gap of CuInS2

  2. Preparation of potassium tantalate niobate thin films by chemical solution deposition and their characterization

    Czech Academy of Sciences Publication Activity Database

    Buršík, Josef; Železný, Vladimír; Vaněk, Přemysl

    2005-01-01

    Roč. 25, č. 12 (2005), s. 2151-2154. ISSN 0955-2219 R&D Projects: GA ČR GA202/02/0238; GA MŠk(CZ) LN00A028; GA MŠk OC 528.001 Institutional research plan: CEZ:AV0Z40320502 Keywords : films * tantalates * chemical solution deposition Subject RIV: CA - Inorganic Chemistry Impact factor: 1.567, year: 2005

  3. Ionic Liquids and Cellulose: Dissolution, Chemical Modification and Preparation of New Cellulosic Materials

    Directory of Open Access Journals (Sweden)

    Mehmet Isik

    2014-07-01

    Full Text Available Due to its abundance and a wide range of beneficial physical and chemical properties, cellulose has become very popular in order to produce materials for various applications. This review summarizes the recent advances in the development of new cellulose materials and technologies using ionic liquids. Dissolution of cellulose in ionic liquids has been used to develop new processing technologies, cellulose functionalization methods and new cellulose materials including blends, composites, fibers and ion gels.

  4. Evaluation of Chemical Preparation on Insect Wing Shape for Geometric Morphometrics

    OpenAIRE

    Lorenz, Camila; Suesdek, Lincoln

    2013-01-01

    Geometric morphometrics is an approach that has been increasingly applied in studies with insects. A limiting factor of this technique is that some mosquitoes have wings with dark spots or many scales, which jeopardizes the visualization of landmarks for morphometric analysis. Recently, in some studies, chemically treatment (staining) of the wings was used to improve the viewing of landmarks. In this study, we evaluated whether this method causes deformation of the wing veins and tested wheth...

  5. Enamels in stained glass windows: Preparation, chemical composition, microstructure and causes of deterioration

    International Nuclear Information System (INIS)

    Stained glass windows incorporating dark blue and purple enamel paint layers are in some cases subject to severe degradation while others from the same period survived the ravages of time. A series of dark blue, green-blue and purple enamel glass paints from the same region (Northwestern Europe) and from the same period (16-early 20th centuries) has been studied by means of a combination of microscopic X-ray fluorescence analysis, electron probe micro analysis and transmission electron microscopy with the aim of better understanding the causes of the degradation. The chemical composition of the enamels diverges from the average chemical composition of window glass. Some of the compositions appear to be unstable, for example those with a high concentration of K2O and a low content of CaO and PbO. In other cases, the deterioration of the paint layers was caused by the less than optimal vitrification of the enamel during the firing process. Recipes and chemical compositions indicate that glassmakers of the 16-17th century had full control over the color of the enamel glass paints they made. They mainly used three types of coloring agents, based on Co (dark blue), Mn (purple) and Cu (light-blue or green-blue) as coloring elements. Blue-purple enamel paints were obtained by mixing two different coloring agents. The coloring agent for red-purple enamel, introduced during the 19th century, was colloidal gold embedded in grains of lead glass.

  6. Cross-cultural counseling with the chemically dependent: preparing for service delivery within a culture of violence.

    Science.gov (United States)

    Wallace, B C

    1993-01-01

    This article prepares the clinician delivering chemical dependency treatment for more effective work in therapeutic dyads where there are racial, ethnic, or other "differences" between client and therapist. The objective is to prepare clinicians for service delivery within the present culture of violence and for the receipt of additional training in cross-cultural counseling and trauma-resolution psychotherapy. Social learning and unconscious processes are reviewed in order to explain how this culture of violence operates and impacts treatment. The way in which chemically dependent clients of color--especially African-Americans, Native Americans, and Latinos--have been impacted by both personal and cultural trauma is illustrated by a case example. The resolution of clients' personal trauma by properly trained clinicians is presented as relapse prevention and the clients' best defense against becoming a victim of violence and racism. The article ends with a brief description of the recommended clinical technique for this kind of work, and a statement of needed research. PMID:8483053

  7. On ultra-thin oxide/Si and very-thin oxide/Si structures prepared by wet chemical process

    International Nuclear Information System (INIS)

    The properties of ultra-thin oxide/Si and very-thin oxide/Si structures prepared by wet chemical oxidation in nitric acid aqueous solutions (NAOS) and passivated in HCN aqueous solutions were investigated by electrical, optical and structural methods. n- and p-doped (1 0 0) crystalline Si substrates were used. There were identified more types of interface defect states in dependence on both post-oxidation treatment and passivation procedure. On samples prepared on n-type Si, continuous spectrum of defect states of 0.05-0.2 eV range and discrete defect traps, ∼ECB - 0.26 eV and ∼ECB - 0.39 eV, were found. All mentioned defects are related with various types of Si dangling bonds and/or with SiOx precipitates. Post-metallization annealing of investigated MOS structures reduced the interface defect density and suppressed the leakage currents. It did not change spectral profile of interface defect states in the Si band gap. In addition, there are presented following two optical phenomena: relation between amplitude of photoluminescence signal of NAOS samples and parameters of chemical oxidation process and quantum confinement effect observed on samples containing Si grains of size less as ∼2 nm.

  8. Determination of photocatalytic activity in amorphous and crystalline titanium oxide films prepared using plasma-enhanced chemical vapor deposition

    Science.gov (United States)

    Wu, Cheng-Yang; Chiang, Bo-Sheng; Chang, Springfield; Liu, Day-Shan

    2011-01-01

    Hydro-oxygenated amorphous titanium oxide (a-TiO x:OH) films were prepared by plasma-enhanced chemical vapor deposition (PECVD) using precursors of titanium tetraisopropoxide (TTIP) and oxygen. The influences of chemical states and crystal quality on the photocatalytic activity were systematically investigated in the as-deposited and post-annealed films. The degree of the photocatalytic activity was deeply correlated with the porosity related to the hydroxyl (OH) groups in the as-deposited amorphous film. The crystallized anatase structures was observed from the 200 °C-deposited a-TiO x:OH film after a post-annealing treatment at 400 °C. The photocatalytic activity related to the film with anatase structure was markedly superior to that of an amorphous film with porous structures. The larger the crystal size of the anatase structure, the higher the photocatalytic activity obtained. At elevated annealed temperatures, the inferior anatase structure due to the crystalline transformation led to a low photocatalytic activity. It was concluded that the photocatalytic activity of an amorphous TiO x film prepared using PECVD was determined by the porosity originating from the functional OH groups in the film, whereas the crystalline quality of anatase phase in the annealed poly-TiO x film was crucial to the photocatalytic activity.

  9. Hydroxyapatite, a biomaterial: Its chemical synthesis, characterization and study of biocompatibility prepared from shell of garden snail, Helix aspersa

    Indian Academy of Sciences (India)

    Anjuvan Singh

    2012-11-01

    The shell of garden snail (Helix aspersa) is basically made of calcium carbonate. An attempt is made to convert calcium carbonate of garden snail shell to hydroxyapatite. The snail shell was found to decompose within 850°C to all the carbonate phases. The calcined snail shells were then treated with acids followed by different chemicals in ammoniacal media maintaining proper stoichiometry to produce fine hydroxyapatite (HAP) as filter cake with a Ca/P molar ratio of 1.67. The dried HAP powder was extremely pure with a specific surface area of 15 m2/g. The different characterization techniques were adopted both for calcined snail shell and HAP synthesized by X-ray diffraction (XRD), thermal analysis (DTA/TGA), Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The surface area and particle size of HAP powder prepared by chemical precipitation route, were also determined by BET and Malvern particle size analyser, respectively. The synthesized powder was soaked in stimulated body fluid (SBF) medium for various periods of time in order to evaluate its bioactivity. The changes of pH of SBF medium were measured. High bioactivity of prepared HAP powder due to the formation of apatite on its surface was observed.

  10. Low temperature preparation of nanocrystalline solid solution of strontium barium niobate by chemical process

    Indian Academy of Sciences (India)

    Asit B Panda; Amita Pathak; Panchanan Pramanik

    2002-11-01

    SrBa1–Nb2O6 (with = 0.4, 0.5 and 0.6) powders have been prepared by thermolysis of aqueous precursor solutions consisting of triethanolamine (TEA), niobium tartarate and, EDTA complexes of strontium and barium ions. Complete evaporation of the precursor solution by heating at ∼ 200°C, yields in a fluffy, mesoporous carbon rich precursor material, which on calcination at 750°C/2 h has resulted in the pure SBN powders. The crystallite and average particle sizes are found to be around 15 nm and 20 nm, respectively.

  11. Studies on preparation and characterization of indium doped zinc oxide films by chemical spray deposition

    Indian Academy of Sciences (India)

    Benny Joseph; P K Manoj; V K Vaidyan

    2005-08-01

    The preparation of indium doped zinc oxide films is discussed. Variation of structural, electrical and optical properties of the films with zinc acetate concentration and indium concentration in the solution are investigated. XRD studies have shown a change in preferential orientation from (002) to (101) crystal plane with increase in indium dopant concentration. Films deposited at optimum conditions have a low resistivity of 1.33 × 10-4 m with 94% transmittance at 550 nm. SEM studies have shown smooth polycrystalline morphology of the films. Figure of merit is evaluated from electrical resistivity and transmittance data.

  12. A non-chemically selective top-down approach towards the preparation of hierarchical TS-1 zeolites with improved oxidative desulfurization catalytic performance.

    Science.gov (United States)

    Du, Shuting; Chen, Xiaoxin; Sun, Qiming; Wang, Ning; Jia, Mingjun; Valtchev, Valentin; Yu, Jihong

    2016-02-28

    Hierarchical TS-1 zeolites with secondary macropores have been successfully prepared by using two different fluoride-containing chemical etching post-treated routes. Hierarchical TS-1 zeolites exhibited a chemical composition similar to that of the parent material and showed remarkably enhanced catalytic activity in oxidative desulfurization reaction. PMID:26846586

  13. Preparation of porous bio-char and activated carbon from rice husk by leaching ash and chemical activation.

    Science.gov (United States)

    Ahiduzzaman, Md; Sadrul Islam, A K M

    2016-01-01

    Preparation porous bio-char and activated carbon from rice husk char study has been conducted in this study. Rice husk char contains high amount silica that retards the porousness of bio-char. Porousness of rice husk char could be enhanced by removing the silica from char and applying heat at high temperature. Furthermore, the char is activated by using chemical activation under high temperature. In this study no inert media is used. The study is conducted at low oxygen environment by applying biomass for consuming oxygen inside reactor and double crucible method (one crucible inside another) is applied to prevent intrusion of oxygen into the char. The study results shows that porous carbon is prepared successfully without using any inert media. The adsorption capacity of material increased due to removal of silica and due to the activation with zinc chloride compared to using raw rice husk char. The surface area of porous carbon and activated carbon are found to be 28, 331 and 645 m(2) g(-1) for raw rice husk char, silica removed rice husk char and zinc chloride activated rice husk char, respectively. It is concluded from this study that porous bio-char and activated carbon could be prepared in normal environmental conditions instead of inert media. This study shows a method and possibility of activated carbon from agro-waste, and it could be scaled up for commercial production. PMID:27536531

  14. Chemical characterization of a potassium hydroxyapatite prepared by soaking in potassium chloride and carbonate solutions.

    Science.gov (United States)

    Nordström, E G; Karlsson, K H

    1992-01-01

    A potassium-doped synthetic apatite was prepared by soaking hydroxyapatite in potassium carbonate and potassium chloride solutions. The hydroxyapatite was prepared by firing slip cast ceramic bodies in vacuum at 1100 degrees C. The conical ceramic samples and a crushed material of this were soaked in carbonate and chloride solutions for 2, 4, 6, and 8 weeks. Potassium, calcium, and phosphate were determined by direct current plasma emission spectroscopy. The carbonate content was determined by thermogravimetric analysis and chloride titrimetrically. After 2 weeks, one potassium ion substituted one calcium ion when soaked in a carbonate solution. When soaked in the chloride solution substitution occurred to the same extent. At phosphate sites the substitution of phosphate for carbonate occurred at one sixth of the sites after 2 weeks. Chloride incorporated one half of the OH-sites after 2 weeks. After 4 weeks about one chloride ion was found in the apatite, and after 6 weeks one and a half of the OH-sites were occupied by chloride ions. PMID:1483120

  15. Preparation and Chemical Properties of π-Conjugated Polymers Containing Indigo Unit in the Main Chain

    Directory of Open Access Journals (Sweden)

    Hiroki Fukumoto

    2014-03-01

    Full Text Available π-Conjugated polymers based on indigo unit were prepared. Dehalogenative polycondensation of N-hexyl-6,6'-dibromoindigo with a zerovalent nickel complex gave a homopolymer, P(HexI, in 77% yield. Copolymer of N-hexyl-indigo and pyridine, P(HexI-Py, was also prepared in 50% yield. P(HexI showed good solubility in organic solvents, whereas P(HexI-Py was only soluble in acids such as HCOOH. The weight-average molecular weights (Mw of P(HexI and P(HexI-Py were determined to be 10,000 and 40,000, respectively, by a light scattering method. Pd-catalyzed polycondensation between 6,6'-dibromoindigo with N-BOC (BOC = t-butoxycarbonyl substituents and a diboronic compound of 9,9-dioctylfluorene afforded the corresponding alternating copolymer, P(BOCI-Flu, as a deep red solid in 98% yield. P(BOCI-Flu was soluble in N-methyl-2-pyrroridone and showed an Mw of 29,000 in GPC analysis. Treatment of P(BOCI-Flu with CF3COOH smoothly led to a BOC-deprotection reaction to give an insoluble deep green polymer, P(I-Flu, in a quantitative yield. Diffuse reflectance spectra of powdery P(BOCI-Flu and P(I-Flu showed peaks at about 580 nm and 630 nm, respectively, which are thought to originate from the indigo unit.

  16. Preparation and characterization of activated carbon from pistachio nut shells via microwave-induced chemical activation

    International Nuclear Information System (INIS)

    In this work, pistachio nut shell, a biomass residue abundantly available from the pistachio nut processing industries, was utilized as a feedstock for the preparation of activated carbon (PSAC) via microwave assisted KOH activation. The activation step was performed at the microwave input power of 600 W and irradiation time of 7 min. The porosity, functional and surface chemistry were featured by means of low temperature nitrogen adsorption, scanning electron microscopy and Fourier transform infrared spectroscopy. Result showed that the BET surface area, Langmuir surface area, and total pore volume of PSAC were 700.53 m2 g-1, 1038.78 m2 g-1 and 0.375 m3 g-1, respectively. The adsorptive property of PSAC was tested using methylene blue dye as the targeted adsorbate. Equilibrium data was best fitted by the Langmuir isotherm model, showing a monolayer adsorption capacity of 296.57 mg g-1. The study revealed the potentiality of microwave-induced activation as a viable activation method. -- Highlights: → Pistachio nut shell activated carbon (PSAC) was prepared via microwave assisted KOH activation. → The activation step was performed at the microwave input power of 600 W and irradiation time of 7 min. → BET surface area of PSAC was 700.53 m2/g. → Monolayer adsorption capacity of PSAC for MB was 296.57 mg/g.

  17. New crosslinked cast films based on poly(vinyl alcohol: Preparation and physico-chemical properties

    Directory of Open Access Journals (Sweden)

    C. Birck

    2014-12-01

    Full Text Available In this paper, we propose a green route to prepare insoluble poly(vinyl alcohol (PVOH cast films with potential application as antimicrobial packaging. First PVOH films were cast from different aqueous solutions and analyzed by Differential Scanning Calorimetry (DSC and Dynamic Mechanical Analysis (DMA to determine their physical properties under two storage conditions. In order to obtain insoluble films, PVOH was then crosslinked by citric acid (CTR as confirmed by Nuclear Magnetic Resonance (NMR analyses. The crosslinking reaction parameters (curing time, crosslinker content were studied by comparing the characteristics of PVOH/CTR films, such as free COOH content and glass transition temperature (Tg value, as well as the impact of the crosslinking reaction on mechanical properties. It was found that for 40 and 10 wt% CTR contents, 120 and 40 min of crosslinking times were necessary to bind all CTR respectively. Brittle films were obtained for 40 wt% CTR whereas 10 wt% CTR content led to ductile films. Finally, films containing hydroxypropyl-β-cyclodextrin (HPβCD, chosen as a potential vector of antimicrobial agent, were prepared. The obtained results show that the incorporation of HPβCD in the PVOH matrix does not mainly influence the physical and mechanical properties of the films.

  18. Chemically prepared La2Se3 nanocubes thin film for supercapacitor application.

    Science.gov (United States)

    Patil, S J; Lokhande, V C; Chodankar, N R; Lokhande, C D

    2016-05-01

    Lanthanum selenide (La2Se3) nanocubes thin film is prepared via successive ionic layer adsorption and reaction (SILAR) method and utilized for energy storage application. The prepared La2Se3 thin film is characterized by X-ray diffraction, field emission scanning electron microscopy and contact angle measurement techniques for structural, surface morphological and wettability studies, respectively. Energy dispersive X-ray microanalysis (EDAX) is performed in order to obtain the elemental composition of the thin film. The La2Se3 film electrode shows a maximum specific capacitance of 363Fg(-1) in a 0.8M LiClO4/PC electrolyte at a scan rate of 5mVs(-1) within 1.3 V/SCE potential range. The specific capacitive retention of 83 % of La2Se3 film electrode is obtained over 1000 cyclic voltammetry cycles. The predominant performance, such as high energy (80Whkg(-1)) and power density (2.5kWkg(-1)), indicates that La2Se3 film electrode facilitates fast ion diffusion during redox processes. PMID:26901380

  19. Evaluation of alternative chemical additives for high-level waste vitrification feed preparation processing

    Energy Technology Data Exchange (ETDEWEB)

    Seymour, R.G.

    1995-06-07

    During the development of the feed processing flowsheet for the Defense Waste Processing Facility (DWPF) at the Savannah River Site (SRS), research had shown that use of formic acid (HCOOH) could accomplish several processing objectives with one chemical addition. These objectives included the decomposition of tetraphenylborate, chemical reduction of mercury, production of acceptable rheological properties in the feed slurry, and controlling the oxidation state of the glass melt pool. However, the DEPF research had not shown that some vitrification slurry feeds had a tendency to evolve hydrogen (H{sub 2}) and ammonia (NH{sub 3}) as the result of catalytic decomposition of CHOOH with noble metals (rhodium, ruthenium, palladium) in the feed. Testing conducted at Pacific Northwest Laboratory and later at the Savannah River Technical Center showed that the H{sub 2} and NH{sub 3} could evolve at appreciable rates and quantities. The explosive nature of H{sub 2} and NH{sub 3} (as ammonium nitrate) warranted significant mitigation control and redesign of both facilities. At the time the explosive gas evolution was discovered, the DWPF was already under construction and an immediate hardware fix in tandem with flowsheet changes was necessary. However, the Hanford Waste Vitrification Plant (HWVP) was in the design phase and could afford to take time to investigate flowsheet manipulations that could solve the problem, rather than a hardware fix. Thus, the HWVP began to investigate alternatives to using HCOOH in the vitrification process. This document describes the selection, evaluation criteria, and strategy used to evaluate the performance of the alternative chemical additives to CHOOH. The status of the evaluation is also discussed.

  20. Radio-frequency inductively coupled plasma-chemical installation for preparation of nanodispersed powders

    International Nuclear Information System (INIS)

    Full text: The wide application of radio-frequency inductively coupled plasma (rf-ICP) is due to the following. Rf-ICPs are clean because these types of plasma do not use any electrode and, hence, are contamination free. Rf-ICPs are stable and can be used over a wide range of operating conditions. They have relatively large volumes and low plasma velocities, which result in complete melting of the solid materials in materials processing because of the longer residence time. The preciseness of the rf-ICPs is important in determining contamination effects (which inevitably occur because of electrode evaporation and nozzle ablation) on gas circuit breaker arcs as well as to predict plasma properties for all materials processing, and any gas or mixture of gases can be excited by the rf fields, so there is wide flexibility when choosing plasma gas(es) depending on the type of application [1].; The experimental plasma set-up used for the production of nanosized powders (carbides, carbon nano-structures (nanotubes, fullerenes), oxides, nitrides, catalysts, pigments, etc.) consists of a radio-frequency generator (maximum power 60 kW, frequency 1+30 MHz), a water-cooled quartz plasma-chemical reactor with inductor, raw powder and gas supply systems, a gas quenching device, heat exchangers and cloth filter for powder collection. Ar, N2, Ar+N2, air, air+O2, and Ar+H2 can be used as plasma-forming gases. The quenching gases are air, Ar, N2, and CO2. The raw powder is injected into the upper part of the plasma-chemical reactor. A chemical reaction is carried out in the reactor and after complete evaporation of the micron size powder, it enters the quenching device. After that, the nanosized product is captured by the heat exchangers and cloth filter

  1. Evaluation of alternative chemical additives for high-level waste vitrification feed preparation processing

    International Nuclear Information System (INIS)

    During the development of the feed processing flowsheet for the Defense Waste Processing Facility (DWPF) at the Savannah River Site (SRS), research had shown that use of formic acid (HCOOH) could accomplish several processing objectives with one chemical addition. These objectives included the decomposition of tetraphenylborate, chemical reduction of mercury, production of acceptable rheological properties in the feed slurry, and controlling the oxidation state of the glass melt pool. However, the DEPF research had not shown that some vitrification slurry feeds had a tendency to evolve hydrogen (H2) and ammonia (NH3) as the result of catalytic decomposition of CHOOH with noble metals (rhodium, ruthenium, palladium) in the feed. Testing conducted at Pacific Northwest Laboratory and later at the Savannah River Technical Center showed that the H2 and NH3 could evolve at appreciable rates and quantities. The explosive nature of H2 and NH3 (as ammonium nitrate) warranted significant mitigation control and redesign of both facilities. At the time the explosive gas evolution was discovered, the DWPF was already under construction and an immediate hardware fix in tandem with flowsheet changes was necessary. However, the Hanford Waste Vitrification Plant (HWVP) was in the design phase and could afford to take time to investigate flowsheet manipulations that could solve the problem, rather than a hardware fix. Thus, the HWVP began to investigate alternatives to using HCOOH in the vitrification process. This document describes the selection, evaluation criteria, and strategy used to evaluate the performance of the alternative chemical additives to CHOOH. The status of the evaluation is also discussed

  2. Quaternary hard nanocomposite TiCxNy/SiCN coatings prepared by plasma enhanced chemical vapor deposition

    International Nuclear Information System (INIS)

    Individual hard thin film materials such as TiN, SiN1.3, SiC and CNx exhibit attractive mechanical, tribological, optical and electronic properties related to their microstructure and chemical bonding. In the present work, we combine the characteristics of such materials, while systematically studying quaternary thin films prepared by plasma enhanced chemical vapor deposition (PECVD) from TiCl4/SiH4/N2/CH4 mixtures with different concentrations of CH4. Detailed structural and chemical characterizations using transmission electron microscopy, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and elastic recoil detection suggest formation of a TiCxNy/SiCN nanocomposite structure. Depth-sensing indentation, static indentation and curvature measurements, on samples prepared under optimal conditions, reveal a hardness of 55 GPa, reduced Young's modulus of 302 GPa, a compressive stress of 2.0 GPa, an elastic rebound of more than 80 %, H3/Er2 coefficient of 1.8 GPa and a high toughness. The friction coefficient and the wear rate, measured against diamond, are 0.13*10-6 and 12*10-6 mm3/Nm, respectively. We compare the properties of the present nanocomposite TiCxNy/SiCN coatings with the performance of PECVD films from our earlier studies: these include TiN/SiN1.3 nanocomposites and SiCN, for which we obtained a hardness of 45 and 33 GPa, and a reduced Young's modulus of 350 and 200 GPa, respectively

  3. Liposomes for topical use: a physico-chemical comparison of vesicles prepared from egg or soy lecithin.

    Science.gov (United States)

    Budai, Lívia; Kaszás, Nóra; Gróf, Pál; Lenti, Katalin; Maghami, Katayoon; Antal, István; Klebovich, Imre; Petrikovics, Ilona; Budai, Marianna

    2013-12-01

    Developments in nanotechnology and in the formulation of liposomal systems provide the opportunity for cosmetic dermatology to design novel delivery systems. Determination of their physico-chemical parameters has importance when developing a nano-delivery system. The present study highlights some technological aspects/characteristics of liposomes formulated from egg or soy lecithins for topical use. Alterations in the pH, viscosity, surface tension, and microscopic/macroscopic appearance of these vesicular systems were investigated. The chemical composition of the two types of lecithin was checked by mass spectrometry. Caffeine, as a model molecule, was encapsulated into multilamellar vesicles prepared from the two types of lecithin: then zeta potential, membrane fluidity, and encapsulation efficiency were compared. According to our observations, samples prepared from the two lecithins altered the pH in opposite directions: egg lecithin increased it while soy lecithin decreased it with increased lipid concentration. Our EPR spectroscopic results showed that the binding of caffeine did not change the membrane fluidity in the temperature range of possible topical use (measured between 2 and 50 °C). Combining our results on encapsulation efficiency for caffeine (about 30% for both lecithins) with those on membrane fluidity data, we concluded that the interaction of caffeine with the liposomal membrane does not change the rotational motion of the lipid molecules close to the head group region. In conclusion, topical use of egg lecithin for liposomal formulations can be preferred if there are no differences in the physico-chemical properties due to the encapsulated drugs, because the physiological effects of egg lecithin vesicles on skin are significantly better than that of soy lecithin liposomes. PMID:24482779

  4. Antibacterial, Structural and Optical Characterization of Mechano-Chemically Prepared ZnO Nanoparticles.

    Science.gov (United States)

    Manzoor, Umair; Siddique, Sumera; Ahmed, Rafay; Noreen, Zobia; Bokhari, Habib; Ahmad, Iftikhar

    2016-01-01

    Structural investigations, optical properties and antibacterial performance of the pure Zinc Oxide (ZnO) nanoparticles (NPs) synthesized by mechano-chemical method are presented. The morphology, dimensions and crystallinity of the ZnO NPs were controlled by tweaking the mechanical agitation of the mixture and subsequent thermal treatment. ZnO nanoparticles in small (Vibrio cholerae as well as Gram positive methicillin resistant Staphylococcus aureus (MRSA), thus potential for medical applications. Scanning electron microscopy and survival assay indicated that most probably ZnO nanoparticles cause changes in cellular morphology which eventually causes bacterial cell death. PMID:27183165

  5. The structure and growth mechanism of Si nanoneedles prepared by plasma-enhanced chemical vapor deposition

    Czech Academy of Sciences Publication Activity Database

    Červenka, Jiří; Ledinský, Martin; Stuchlík, Jiří; Stuchlíková, The-Ha; Bakardjieva, Snejana; Hruška, Karel; Fejfar, Antonín; Kočka, Jan

    2010-01-01

    Roč. 21, č. 41 (2010), 415604/1-415604/7. ISSN 0957-4484 R&D Projects: GA MŠk(CZ) LC06040; GA AV ČR KAN400100701; GA MŠk LC510 EU Projects: European Commission(XE) 240826 - POLYSIMODE Institutional research plan: CEZ:AV0Z10100521; CEZ:AV0Z40320502 Keywords : nanoneedles * nanowires * silicon * plasma * chemical vapor deposition * crystal structure * growth * phonon * SEM * Raman Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 3.644, year: 2010

  6. Preparation of Dispersed Platinum Nanoparticles on a Carbon Nanostructured Surface Using Supercritical Fluid Chemical Deposition

    Directory of Open Access Journals (Sweden)

    Mineo Hiramatsu

    2010-03-01

    Full Text Available We have developed a method of forming platinum (Pt nanoparticles using a metal organic chemical fluid deposition (MOCFD process employing a supercritical fluid (SCF, and have demonstrated the synthesis of dispersed Pt nanoparticles on the surfaces of carbon nanowalls (CNWs, two-dimensional carbon nanostructures, and carbon nanotubes (CNTs. By using SCF-MOCFD with supercritical carbon dioxide as a solvent of metal-organic compounds, highly dispersed Pt nanoparticles of 2 nm diameter were deposited on the entire surface of CNWs and CNTs. The SCF-MOCFD process proved to be effective for the synthesis of Pt nanoparticles on the entire surface of intricate carbon nanostructures with narrow interspaces.

  7. Composition and structure of chemically prepared GaAs(1 1 1)A and (1 1 1)B surfaces

    Science.gov (United States)

    Tereshchenko, O. E.; Alperovich, V. L.; Terekhov, A. S.

    2006-02-01

    The (1 1 1)A and (1 1 1)B surfaces of GaAs chemically treated in HCl-isopropanol solution (HCl-iPA) and annealed in vacuum were studied by means of X-ray photoelectron spectroscopy (XPS), low-energy electron diffraction (LEED) and electron energy loss spectroscopy (EELS). To avoid uncontrolled contamination, chemical treatment and sample transfer into UHV were performed under pure nitrogen atmosphere. The HCl-iPA treatment removes gallium and arsenic oxides, with about 0.5-3 ML of elemental arsenic being left on the surface, depending on the crystallographic orientation. With the increase of the annealing temperature, a sequence of reconstructions were identified by LEED: (1 × 1) and (2 × 2) on the (1 1 1)A surface and (1 × 1), (2 × 2), (1 × 1), (3 × 3), (√19 × √19) on the (1 1 1)B surface. These sequences of reconstructions correspond to the decrease of surface As concentration. The structural properties of chemically prepared GaAs(1 1 1) surfaces were found to be similar to those obtained by decapping of As-capped epitaxial layers.

  8. Transparent conducting oxide films of group V doped titania prepared by aqueous chemical solution deposition

    Energy Technology Data Exchange (ETDEWEB)

    Elen, Ken [Inorganic and Physical Chemistry, Institute for Materials Research, Hasselt University, Agoralaan Building D, B-3590 Diepenbeek (Belgium); IMEC vzw division IMOMEC, Agoralaan Building D, B-3590 Diepenbeek (Belgium); Strategisch Initiatief Materialen (SIM), SoPPoM Program (Belgium); Capon, Boris [Strategisch Initiatief Materialen (SIM), SoPPoM Programm (Belgium); Coating and Contacting of Nanostructures, Ghent University, Krijgslaan 281 S1, B-9000 Ghent (Belgium); De Dobbelaere, Christopher [Inorganic and Physical Chemistry, Institute for Materials Research, Hasselt University, Agoralaan Building D, B-3590 Diepenbeek (Belgium); Dewulf, Daan [Inorganic and Physical Chemistry, Institute for Materials Research, Hasselt University, Agoralaan Building D, B-3590 Diepenbeek (Belgium); IMEC vzw division IMOMEC, Agoralaan Building D, B-3590 Diepenbeek (Belgium); Peys, Nick [Inorganic and Physical Chemistry, Institute for Materials Research, Hasselt University, Agoralaan Building D, B-3590 Diepenbeek (Belgium); IMEC vzw, Kapeldreef 75, B-3001 Heverlee (Belgium); Detavernier, Christophe [Coating and Contacting of Nanostructures, Ghent University, Krijgslaan 281 S1, B-9000 Ghent (Belgium); Hardy, An [Inorganic and Physical Chemistry, Institute for Materials Research, Hasselt University, Agoralaan Building D, B-3590 Diepenbeek (Belgium); IMEC vzw division IMOMEC, Agoralaan Building D, B-3590 Diepenbeek (Belgium); Van Bael, Marlies K., E-mail: marlies.vanbael@uhasselt.be [Inorganic and Physical Chemistry, Institute for Materials Research, Hasselt University, Agoralaan Building D, B-3590 Diepenbeek (Belgium); IMEC vzw division IMOMEC, Agoralaan Building D, B-3590 Diepenbeek (Belgium)

    2014-03-31

    Transparent conducting oxide (TCO) films of titania doped with vanadium (V), niobium (Nb) and tantalum (Ta) are obtained by aqueous Chemical Solution Deposition (CSD). The effect of the dopant on the crystallization and microstructure of the resulting films is examined by means of X-ray diffraction and electron microscopy. During annealing of the thin films, in-situ characterization of the crystal structure and sheet resistance is carried out. Niobium doped anatase films, obtained after annealing in forming gas, show a resistivity of 0,28 Ohm cm, which is the lowest resistivity reported for a solution deposited anatase-based TCO so far. Here, we demonstrate that aqueous CSD may provide a strategy for scalable TCO production in the future. - Highlights: • Aqueous chemical solution deposition of doped titanium dioxide • Doping delays the phase transition from anatase to rutile • Lowest resistivity after doping with niobium and annealing in Forming Gas • Transparency higher than 80% in the visible range of optical spectrum.

  9. Transparent conducting oxide films of group V doped titania prepared by aqueous chemical solution deposition

    International Nuclear Information System (INIS)

    Transparent conducting oxide (TCO) films of titania doped with vanadium (V), niobium (Nb) and tantalum (Ta) are obtained by aqueous Chemical Solution Deposition (CSD). The effect of the dopant on the crystallization and microstructure of the resulting films is examined by means of X-ray diffraction and electron microscopy. During annealing of the thin films, in-situ characterization of the crystal structure and sheet resistance is carried out. Niobium doped anatase films, obtained after annealing in forming gas, show a resistivity of 0,28 Ohm cm, which is the lowest resistivity reported for a solution deposited anatase-based TCO so far. Here, we demonstrate that aqueous CSD may provide a strategy for scalable TCO production in the future. - Highlights: • Aqueous chemical solution deposition of doped titanium dioxide • Doping delays the phase transition from anatase to rutile • Lowest resistivity after doping with niobium and annealing in Forming Gas • Transparency higher than 80% in the visible range of optical spectrum

  10. Preparation, quality control and physico-chemical properties of 99mTc-BAT-AV-45

    International Nuclear Information System (INIS)

    One novel styrylpyridine derivatives(AV-45) coupled with 99mTc complex was synthesized. 99mTc-BAT-AV-45 was prepared by a ligand exchange reaction employing sodium glucoheptonate, and effects of the amount of ligand, stannous chloride, sodium glucoheptonate and pH value of reaction mixture on the radiolabeling yield were studied in details. Quality control was performed by thin layer chromatography and high performance liquid chromatography. Besides the stability, partition coefficient and electrophoresis of 99mTc-BAT-AV-45 were also investigated. The results showed that the average radiolabeling yield was (95 ± 1%) and 99mTc-BAT-AV-45 with suitable lipophilicity was stable and uncharged at physiological pH. (author)

  11. Nanoglass Fe79B21 powders prepared by chemical reduction: a low-temperature mossbauer study

    DEFF Research Database (Denmark)

    Wu, G.Y.; Jiang, Jianzhong; Lin, X.P.

    1999-01-01

    The magnetic behavior of nanoglass Fe79B21 powder has been investigated by Mossbauer spectroscopy in a temperature range from 5 to 295 K together with one amorphous Fe80B20 ribbon prepared by melt-spinning. It is found that average hyperfine fields for the powder sample are smaller than those for...... the ribbon sample in the whole temperature range studied. The reduced average hyperfine field of nanoglass Fe79B21 powders follows the Bloch's law, H(T)/H(0)=1-BT3/2. The B paramaters for the powder and the ribbon samples are found to be about 2.8 x 10-5K3/2 and 2.2 x 10-5K3/2, respectively...

  12. Preparation and characterization of biomorphic SiC hollow fibers from wood by chemical vapor infiltration

    International Nuclear Information System (INIS)

    Biomorphic SiC hollow fibers were prepared by the reactive infiltration of SiO vapor into basswood-derived charcoal. Gaseous SiO was produced from a SiO2/Si powder mixture in Ar at elevated temperatures. Scanning electron microscopy, energy dispersive X-ray spectroscopy, X-ray diffraction and Fourier transform-infrared spectroscopy were employed to characterize the structural morphology and phase compositions of the final products. The results show that the tubular cells in bulk charcoal are converted into lots of SiC hollow fibers with pore diameters of 10-50 μm and lengths ranging from hundreds of μm to several mm. Resulting SiC hollow fibers consist of β-SiC with a minute amount of α-SiC. The formation mechanism of SiC hollow fibers is based on the gas-solid reaction between SiO and carbon

  13. Chemical and biochemical characterisation of biochar-blended composts prepared from poultry manure.

    Science.gov (United States)

    Jindo, Keiji; Suto, Koki; Matsumoto, Kazuhiro; García, Carlos; Sonoki, Tomonori; Sanchez-Monedero, Miguel A

    2012-04-01

    The aim of this study was to assess the effect of a 2% (v/v) addition of biochar on the quality of a composting mixture prepared with poultry manure and different local organic wastes (rice husk and apple pomace). Compost quality was evaluated in terms of typical stabilisation indices, the microbial biomass and selected enzymatic activities related to the C, N and P cycles. The main effects of biochar were a 10% increase in C captured by humic substance extraction and a 30% decrease of water-soluble C, due to an enhanced degradation rate and/or the sorption of these labile compounds into the biochar. The urease, phosphatase and polyphenol oxidase activities of the biochar-blended compost were enhanced by 30-40% despite the lower amount of microbial biomass. Denaturing gradient gel electrophoresis revealed a higher diversity of fungi in biochar-amended compost, suggesting a change in microbial composition compared to the unamended compost. PMID:22377478

  14. Effect of indium doping on zinc oxide films prepared by chemical spray pyrolysis technique

    Indian Academy of Sciences (India)

    Girjesh Singh; S B Shrivastava; Deepti Jain; Swati Pandya; T Shripathi; V Ganesan

    2010-10-01

    We report the conducting and transparent In doped ZnO films fabricated by a homemade chemical spray pyrolysis system (CSPT). The effect of In concentration on the structural, morphological, electrical and optical properties have been studied. These films are found to show (0 0 2) preferential growth at low indium concentrations. An increase in In concentration causes a decrease in crystalline quality of films as confirmed by X-ray diffraction technique which leads to the introduction of defects in ZnO. Indium doping also significantly increased the electron concentrations, making the films heavily type. However, the crystallinity and surface roughness of the films decreases with increase in indium doping content likely as a result of the formation of smaller grain size, which is clearly displayed in AFM images. Typical optical transmittance values in the order of (80%) were obtained for all films. The lowest resistivity value of 0.045 -m was obtained for film with 5% indium doping.

  15. Biological functionalization and patterning of porous silicon prepared by Pt-assisted chemical etching

    International Nuclear Information System (INIS)

    Porous silicon fabricated via Pt-assisted chemical etching of p-type Si (1 0 0) in 1:1:1 EtOH/HF/H2O2 solution possesses a longer durability in air and in aqueous media than anodized one, which is advantageous for biomedical applications. Its surface SiHx (x = 1 and 2) species can react with 10-undecylenic acid completely under microwave irradiation, and subsequent derivatizations of the end carboxylic acid result in affinity capture of proteins. We applied two approaches to produce protein microarrays: photolithography and spotting. The former provides a homogeneous microarray with a very low fluorescence background, while the latter presents an inhomogeneous microarray with a high noise background.

  16. Deposition and characterization of Ru thin films prepared by metallorganic chemical vapor deposition

    CERN Document Server

    Kang, S Y; Lee, S K; Hwang, C S; Kim, H J

    2000-01-01

    Ru thin films were deposited at 300 approx 400 .deg. C by using Ru(C sub 5 H sub 4 C sub 2 H sub 5) sub 2 (Ru(EtCp) sub 2) as a precursor and low-pressure metalorganic chemical vapor deposition. The addition of O sub 2 gas was essential to form Ru thin films. The deposition rates of the films were about 200 A/min. For low oxygen addition and high substrate temperature, RuO sub 2 phases were formed. Also, thermodynamic calculations showed that all the supplied oxygen was consumed to oxidize carbon and hydrogen, cracked from the precursor ligand, rather than Ru. Thus, metal films could be obtained There was an optimum oxygen to precursor ratio at which the pure Ru phase could be obtained with minimum generation of carbon and RuO sub 2

  17. Methanol sensing by SnO2 pellets prepared by chemical route method

    Science.gov (United States)

    Choudhury, Sandip Paul; Kumari, Navnita; Bhattacharjee, Debanjan; Bhattacharjee, Ayon

    2016-05-01

    Synthesis of SnO2 and SnO2-CuO doped nanoparticles were carried out using chemical co-precipitation method. The precursor was SnCl4.5H2O. The XRD, SEM and EDAX of the nanoparticles were done, and the particle size was confirmed to be within 40nm. The powdered nanoparticles were then pelletized under a pressure of 13 Mp. Methanol was sensed with the pellets using a customized setup for 25, 50, 75 and 100ppm concentrations. It was observed that the sensitivity (S = Ra/Rg) showed appreciable variation at 375 °C and 275 °C for 75ppm and 100ppm of methanol respectively.

  18. Fabrication and Photovoltaic Characteristics of Coaxial Silicon Nanowire Solar Cells Prepared by Wet Chemical Etching

    Directory of Open Access Journals (Sweden)

    Chien-Wei Liu

    2012-01-01

    Full Text Available Nanostructured solar cells with coaxial p-n junction structures have strong potential to enhance the performances of the silicon-based solar cells. This study demonstrates a radial junction silicon nanowire (RJSNW solar cell that was fabricated simply and at low cost using wet chemical etching. Experimental results reveal that the reflectance of the silicon nanowires (SNWs declines as their length increases. The excellent light trapping was mainly associated with high aspect ratio of the SNW arrays. A conversion efficiency of ∼7.1% and an external quantum efficiency of ∼64.6% at 700 nm were demonstrated. Control of etching time and diffusion conditions holds great promise for the development of future RJSNW solar cells. Improving the electrode/RJSNW contact will promote the collection of carries in coaxial core-shell SNW array solar cells.

  19. Homogeneous nanocrystalline cubic silicon carbide films prepared by inductively coupled plasma chemical vapor deposition.

    Science.gov (United States)

    Cheng, Qijin; Xu, S; Long, Jidong; Huang, Shiyong; Guo, Jun

    2007-11-21

    Silicon carbide films with different carbon concentrations x(C) have been synthesized by inductively coupled plasma chemical vapor deposition from a SiH(4)/CH(4)/H(2) gas mixture at a low substrate temperature of 500 °C. The characteristics of the films were studied by x-ray photoelectron spectroscopy, x-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscopy, Fourier transform infrared absorption spectroscopy, and Raman spectroscopy. Our experimental results show that, at x(C) = 49 at.%, the film is made up of homogeneous nanocrystalline cubic silicon carbide without any phase of silicon, graphite, or diamond crystallites/clusters. The average size of SiC crystallites is approximately 6 nm. At a lower value of x(C), polycrystalline silicon and amorphous silicon carbide coexist in the films. At a higher value of x(C), amorphous carbon and silicon carbide coexist in the films. PMID:21730481

  20. Formation and chemical reactivity of carbon fibers prepared by defluorination of graphite fluoride

    Science.gov (United States)

    Hung, Ching-Cheh

    1994-01-01

    Defluorination of graphite fluoride (CFX) by heating to temperatures of 250 to 450 C in chemically reactive environments was studied. This is a new and possibly inexpensive process to produce new carbon-based materials. For example, CF 0.68 fibers, made from P-100 carbon fibers, can be defluorinated in BrH2C-CH = CH-CH2Br (1,4-dibromo-2butene) heated to 370 C, and graphitized to produce fibers with an unusually high modulus and a graphite layer structure that is healed and cross-linked. Conversely, a sulfur-doped, visibly soft carbon fiber was produced by defluorinating CF 0.9 fibers, made from P-25, in sulfur (S) vapor at 370 C and then heating to 660 C in nitrogen (N2). Furthermore, defluorination of the CF 0.68 fibers in bromine (Br2) produced fragile, structurally damaged carbon fibers. Heating these fragile fibers to 1100 C in N2 caused further structural damage, whereas heating to 150 C in bromoform (CHBr3) and then to 1100 C in N2 healed the structural defects. The defluorination product of CFX, tentatively called activated graphite, has the composition and molecular structure of graphite, but is chemically more reactive. Activated graphite is a scavenger of manganese (Mn), and can be intercalated with magnesium (Mg). Also, it can easily collect large amounts of an alloy made from copper (Cu) and type 304 stainless steel to form a composite. Finally, there are indications that activated graphite can wet metals or ceramics, thereby forming stronger composites with them than the pristine carbon fibers can form.

  1. Study of Chemical Treatment Combined with Radiation to Prepare Biotic Elicitor for Utilization in Agriculture

    International Nuclear Information System (INIS)

    Chitosan was prepared from shrimp shell (alpha chitosan) and from squid pen (beta chitosan) with degree of deacetylation of about 70%. Degradation of chitosan in flake form by combined treatment with H2O2 and gamma Co-60 radiation was carried out. Results showed that combined treatment was highly effective for degradation of chitosan to obtain low molecular weight of 1-2 × 105. Oligochitosan was prepared by irradiation of chitosan solution of 50g/l (5%, w/v). The dose required for oligochitosan with water soluble content of more than 70% was of 32kGy and 48kGy for beta and alpha chitosan, respectively. Synergic effect of degradation of chitosan in solution with H2O2 and gamma Co-60 radiation was also investigated. The dose to obtain oligochitosan was reduced from 32kGy to 4kGy for beta chitosan and from 48kGy to 8kGy for alpha chitosan. The elicitation and growth promotion effect of oligochiotsan for sugarcane and rice were investigated. Results showed that oligochitosan with water soluble content of 70-80% (Mw~5,000-10,000) exhibited the most effective elicitation and growth promotion for plant. The optimum oligochitosan concentration by spraying was of 30 and 15ppm for sugarcane and rice, respectively. The disease index of Ustilgo scitaminea and Collectotrichum falcatum on sugarcane were reduced to 44.5 and 72.3% compared to control (100%). The productivity of sugarcane was increased about 13% (8tons/ha). The disease index of Pyricularia grisea on rice was reduced to 53.0% for leaf and 34.1% for neck of bloom compared to control (100%). The productivity of rice was increased for 11-26% (0.6-1.4 tons/ha). The obtained results indicated that oligochitosan is promising to use as a biotic elicitor for plant particularly for sugarcane and rice. The procedure for production of oligochitosan elicitor by γ- irradiation method was described. (author)

  2. Preparation and Performance of Rare Earths Chemical Conversion Film on Magnesium Alloy

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Golden yellow cerium conversion film was obtained on magnesium alloys surface by immersion method and the preparation parameters were established. The influence of different process parameters on the surface morphology and performance of the conversion film were analyzed by means of SEM and electrochemical method. Formation dynamics about cerium conversion film on magnesium alloy in solution containing cerium salt and the anti-corrosion behavior of the conversion film in 3.5% NaCl solution were studied by electrochemical method respectively. The results shows that the conversion film is more compact at room temperature when concentration of cerium sulfate is 10 g·L-1 in the solution; the open circuit potential of the magnesium sample moves up to positive direction about 100 mV, the surface of conversion film becomes even and lustrous, and the adhesion intensity of conversion film increases when adding aluminum nitrate into the solution containing cerium salt. The pH value of the solution and immersion time of the sample in the solution also affect the surface morphology and anti-corrosion property of the conversion film. After covered by rare earths conversion film, the anti-corrosion property of magnesium alloy is obviously improved. Rare earth conversion film has self-repairing capability in corrosion medium.

  3. Physico-chemical, optical and electrochemical properties of iron oxide thin films prepared by spray pyrolysis

    International Nuclear Information System (INIS)

    Iron oxide thin films were prepared by spray pyrolysis technique onto glass substrates from iron chloride solution. They were characterized by X-ray diffractometry (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and (UV-vis) spectroscopy. The films deposited at T s ≤ 450 deg. C were amorphous; while those produced at T sub = 500 deg. C were polycrystalline α-Fe2O3 with a preferential orientation along the (1 0 4) direction. By observing scanning electron microscopy (SEM), it was seen that iron oxide films were relatively homogeneous uniform and had a good adherence to the glass substrates. The grain size was found (by RX) between 19 and 25 nm. The composition of these films was examined by X-ray photoelectron spectroscopy and electron probe microanalysis (EPMA). These films exhibited also a transmittance value about 80% in the visible and infrared range. The cyclic voltammetry study showed that the films of Fe2O3 deposited on ITO pre-coated glass substrates were capable of charge insertion/extraction when immersed in an electrolyte of propylene carbonate (PC) with 0.5 M LiCLO4

  4. Effect of Preparation Conditions on the Crystallinity of Chemically Synthesized BCNO Nanophosphor

    Institute of Scientific and Technical Information of China (English)

    Lakhwant Singh; Viblla Chopra

    2011-01-01

    The carbon based boron oxynitride (BCNO) phosphor was synthesized by solid state reaction between boric acid (H3BO3) and melamine (C3H6N6) in the molar ratios of 1:1 and 2:1 respectively at different temperatures up to 1400℃. The composition with molar ratios 1:1 of starting materials is found to be highly crystalline with an average particle size of 38 nm and the lattice constants a=b=0.251 nm and c=0.666 nm. The solid state reaction of boric acid and melamine in the composition 2:1 leads to the formation of compound in the semi-crystalline state under the same conditions of preparation, but its phase cannot be recognised. The X-ray diffraction (XRD) spectra, transmission electron microscopy (TEM) and scanning electron microscopy (SEM) images of BCNO compound confirm the phase, nanometre size and shape respectively of synthesized material. The photoluminescence (PL) spectra of the synthesized BCNO products reveals that the electronic structure of BCNO compound can be controlled by changing the molar ratios of starting materials and heating temperatures. These synthesized compounds are very interesting and important candidate materials for light emitter.

  5. Preparation and Characterization of SnO2 thin films deposited by Chemical Bath Deposition method

    Science.gov (United States)

    Yusuf, Gbadebo T.; Raimi, Adepoju M.; Familusi, Timothy O.; Awodugba, Ayodeji O.; Efunwole, Hezekiah O.

    2013-04-01

    SnO2 thin films have been deposited onto the soda lime glass substrates by the chemical bath deposition method. The structural and optical properties of the SnO2 thin films were investigated. Tin chloride solution (SnCl2) and methanol were used as starting materials at substrate temperature 300^oC. The crystal structure and orientation of the SnO2 thin films were investigated by X-ray diffraction (XRD) patterns. The average grain size of the films was calculated using the Scherer formula and was found to be 29.6 nm which increased to 30.04nm after annealing in air at 400^oC. The optical absorbance and transmittance measurements were recorded by using spectrophotometer. The average transmittance of the film was around 80 % at wavelength 550 nm. The optical band gap of the thin films was determined and found to be 3.71eV. The gas sensing properties of tin oxide thin films obtained in this work could be performed for different gases like CO, CH4, H2S, H2 etc.

  6. Plasmon-mediated photocatalytic activity of wet-chemically prepared ZnO nanowire arrays.

    Science.gov (United States)

    Dao, Thang Duy; Han, Gui; Arai, Nono; Nabatame, Toshihide; Wada, Yoshiki; Hoang, Chung Vu; Aono, Masakazu; Nagao, Tadaaki

    2015-03-21

    We report on measurements and simulations of the efficient sunlight-driven and visible-active photocatalysts composed of plasmonic metal nanoparticles and ZnO nanowire (NW) arrays fabricated via an all-wet-chemical route. Because of the coupling between the ZnO dielectric response and the excitation of the Ag or Au nanoparticles, efficient electronic excitation can be induced in the vicinity of the metal-ZnO interfaces because optically-excited plasmonic particles can not only concentrate the electromagnetic field at the ZnO/particle interface, but also act as efficient sources of plasmonic hot electrons to be injected into the conduction band of the ZnO catalyst. The catalytic activities of the fabricated ZnO NWs are examined by photodegradation of methylene blue and by photocurrent measurements in a photovoltaic configuration. Numerical electromagnetic simulations were used to understand the behavior of the light on the nanometer-scale to clarify the catalytic enhancement mechanisms in both the ultraviolet (UV) and visible (VIS) regions. In addition, simulation results indicated that a near-surface normal but slightly tilted ZnO NW array geometry would provide an increased optical path length and enhanced multiple scattering and absorption processes arising from the localized surface plasmon resonances of the nanoparticles. The results obtained here clarify the role of the plasmon resonance and provide us with useful knowledge for the development of metal-oxide nano-hybrid materials for solar energy conversion. PMID:25700130

  7. (001) Oriented piezoelectric films prepared by chemical solution deposition on Ni foils

    Energy Technology Data Exchange (ETDEWEB)

    Yeo, Hong Goo, E-mail: hxy162@psu.edu; Trolier-McKinstry, Susan [Materials Research Institute, The Pennsylvania State University, University Park, Pennsylvania 16802 (United States)

    2014-07-07

    Flexible metal foil substrates are useful in some microelectromechanical systems applications including wearable piezoelectric sensors or energy harvesters based on Pb(Zr,Ti)O₃ (PZT) thin films. Full utilization of the potential of piezoelectrics on metal foils requires control of the film crystallographic texture. In this study, (001) oriented PZT thin films were grown by chemical solution deposition (CSD) on Ni foil and Si substrates. Ni foils were passivated using HfO₂ grown by atomic layer deposition in order to suppress substrate oxidation during subsequent thermal treatment. To obtain the desired orientation of PZT film, strongly (100) oriented LaNiO₃ films were integrated by CSD on the HfO₂ coated substrates. A high level of (001) LaNiO₃ and PZT film orientation were confirmed by X-ray diffraction patterns. Before poling, the low field dielectric permittivity and loss tangents of (001) oriented PZT films on Ni are near 780 and 0.04 at 1 kHz; the permittivity drops significantly on poling due to in-plane to out-of-plane domain switching. (001) oriented PZT film on Ni displayed a well-saturated hysteresis loop with a large remanent polarization ~36 μC/cm², while (100) oriented PZT on Si showed slanted P-E hysteresis loops with much lower remanent polarizations. The |e{sub 31,f}| piezoelectric coefficient was around 10.6 C/m² for hot-poled (001) oriented PZT film on Ni.

  8. Preparation and chemical characterization of neodymium-doped molybdenum oxide films grown using spray pyrolysis

    International Nuclear Information System (INIS)

    We studied the crystalline, morphology, and surface composition of Nd-doped molybdenum oxide films grown on glass slides through spray pyrolysis. After fabrication, the films were subjected to thermal treatment in oxygen for periods ranging from 2 to 20 hours. The films were structurally characterized though X-ray diffraction (XRD), their bulk chemical composition was determined using Energy-Dispersive X-ray analysis (EDX), and their surface composition was determined using X-ray Photoelectron Spectroscopy (XP S). The XRD results show that the films obtained from different dissolution volumes and at substrate temperature of 300 grades C exhibit the characteristics of the oxygen-deficient molybdenum trioxide Mo9O26 phase. The films subjected to different thermal treatments exhibit a mixture of Mo9O26 and Mo17O47 phases. EDX study shows the energy belonging to the L line of Nd. Finally, films doped with Nd and subjected to a thermal treatment of 20 h were analyzed through XP S, showing the binding energies at the crystalline lattice correspond to Nd2 (MoO4)3 and Nd2Mo2O7. (Author)

  9. Preparation of intact chloroplasts by chemically induced lysis of the green alga Dunaliella marina.

    Science.gov (United States)

    Kombrink, E; Wöber, G

    1980-07-01

    A method for the isolation in high yield of intact chloroplasts from the unicellular green alga Dunaliella marina (Volvocales) is described. This procedure uses chemically induced lysis of cells with the polycationic macromolecules, DEAE-dextran (M=500,000) or poly-D,L-lysine (M=30,000-70,000). Reaction conditions were optimized with respect to obtaining a high yield of intact chloroplasts, after isopycnic centrifugation in a linear sucrose density gradient, by varying the concentration of polycation and the temperature and pH of incubation. Broken chloroplasts devoid of the stromal marker enzymes fructosebisphosphate phosphatase and ribulosebisphosphate carboxylase, but containing mitochondrial (fumarase) and microbody (catalase) contamination, were banded at a bouyant density of 1.18 g cm(-3). Intact chloroplasts, as indicated by their retention of alkaline fructosebisphosphate phosphatase and ribulosebisphosphate carboxylase, were found in 30% yield (chlorophyll in intact cells, 100%) at an equilibrium density of 1.24 g cm(-3). Contamination by cytoplasmic material (pyruvate kinase), mitochondria, and microbodies was less than 8% each. PMID:24306242

  10. Thermo-physical property measurement of nano-gold dispersed water based nanofluids prepared by chemical precipitation technique.

    Science.gov (United States)

    Paul, G; Pal, T; Manna, I

    2010-09-01

    Nano-gold dispersed water based nanofluid has been prepared following the chemical reduction method. Crystallite size, particle size/shape/morphology, and purity of the nanoparticles have been characterized using X-ray diffraction, scanning and transmission electron microscopy and energy dispersion spectroscopy, respectively. The degree of thermal conductivity enhancement of the nanofluid (with respect to the base fluid) as a function of concentration and size of gold nanoparticle has been determined using the transient hot-wire technique. The degree of enhancement increases with increase in concentration and decrease in size of nanoparticles. The maximum enhancement recorded is approximately 48% at 0.00026 vol.% concentration and 21nm average particle size. PMID:20609848

  11. TEXTURAL AND CHEMICAL CHARACTERISATION OF ACTIVATED CARBONS PREPARED FROM RICE HUSK (ORYZA SATIVA USING A TWO- STAGE ACTIVATION PROCESS

    Directory of Open Access Journals (Sweden)

    JOSEPH G. COLLIN

    2008-12-01

    Full Text Available Activated carbons from agro-industrial wastes; rice husk; were prepared by physical and chemical activation using phosphoric acid as the dehydrating agent. A two-stage activation process method was used; with semi-carbonisation stage at 200oC for 15 minutes as the first stage followed by an activation stage at 500oC for 45 minutes as the second stage. The precursor material with the impregnation agent was exposed straightaway to semi-carbonization and activation temperature unlike the specific temperature progression as reported in the literature. All experiments were conducted in a laboratory scale muffle furnace under static conditions in a self generated atmosphere covering process parameters such as impregnation ratios. We found that by using this method, the AC5 had the highest iodine number and methylene blue adsorption capacity which was 506.6 mg/g and 319.0 mg/g respectively.

  12. Spark plasma sintering of cBN(core/SiO2(shell powder prepared by rotary chemical vapor deposition

    Directory of Open Access Journals (Sweden)

    Jianfeng Zhang

    2014-09-01

    Full Text Available SiO2 nanolayer coated cubic boron nitride (cBN, cBN(core/SiO2(shell powder, was prepared by rotary chemical vapor deposition. The cBN/SiO2 powder was densified by spark plasma sintering at 1873 K for 0.3 ks. The hexagonal boron nitride (hBN phase was not observed in the cBN–SiO2 composites, indicating that the SiO2 nanolayer depressed the phase transformation from cBN to hBN. The relative density of cBN–SiO2 increased with increasing SiO2 content (CSiO2. The highest hardness of the cBN–SiO2 composite was 17.5 GPa at CSiO2=38 wt% and a load of 0.98 N.

  13. Structural and optical properties of Ni-doped CdS thin films prepared by chemical bath deposition method

    International Nuclear Information System (INIS)

    The structural and optical behavior of undoped Cadmiun Sulphide (CdS) and Ni-doped CdS thinfilms prepared by Chemical Bath Deposition (CBD) technique is reported. The crystallite sizes of the thinfilms have been characterized by X-ray diffraction pattern (XRD). The particle sizes increase with the increase of Ni content in the CdS thinfilms. Scanning Electron Microscope (SEM) results indicated that CdS thinfilms is made up of aggregate of spherical-like particles. The composition was estimated by Energy Dispersive Analysis of X-ray (EDX) and reported. Spectroscopic studies revealed considerable improvement in transmission and the band gap of the films changes with addition of Ni dopant that is associated with variation in crystallite sizes in the nano regime

  14. Passivated graphene transistors fabricated on a millimeter-sized single-crystal graphene film prepared with chemical vapor deposition

    International Nuclear Information System (INIS)

    In this work, we first investigate the effects of partial pressures and flow rates of precursors on the single-crystal graphene growth using chemical vapor depositions on copper foils. These factors are shown to be critical to the growth rate, seeding density and size of graphene single crystals. The prepared graphene films in millimeter sizes are then bubbling transferred to silicon-dioxide/silicon substrates for high-mobility graphene transistor fabrications. After high-temperature annealing and hexamethyldisilazane passivation, the water attachment is removed from the graphene channel. The elimination of uncontrolled doping and enhancement of carrier mobility accompanied by these procedures indicate that they are promising for fabrications of graphene transistors. (paper)

  15. Preparation of betulinic acid derivatives by chemical and biotransformation methods and determination of cytotoxicity against selected cancer cell lines.

    Science.gov (United States)

    Baratto, Leopoldo C; Porsani, Mariana V; Pimentel, Ida C; Pereira Netto, Adaucto B; Paschke, Reinhard; Oliveira, Brás H

    2013-10-01

    Several novel 2,4-dinitrophenylhydrazone betulinic acid derivatives have been prepared by chemical and biotransformation methods using fungi and carrot cells. Some compounds showed significant cytotoxicity and selectivity against some tumor cell lines. The most active, 3-[(2,4-dinitrophenyl)hydrazono]lup-(20R)-29-oxolupan-28-oic acid, showed IC50 values between 1.76 and 2.51 μM against five human cancer cell lines. The most selective, 3-hydroxy-20-[(2,4-dinitrophenyl)hydrazono]-29-norlupan-28-oic acid, was five to seven times more selective for cancer cells when compared to fibroblasts. Cell cycle analysis and apoptosis induction were studied for the most active derivatives. PMID:23973824

  16. Preparation of glasses in the Ge-S-I system by plasma-enhanced chemical vapor deposition

    Science.gov (United States)

    Mochalov, L. A.; Churbanov, M. F.; Velmuzhov, A. P.; Lobanov, A. S.; Kornev, R. A.; Sennikov, G. P.

    2015-08-01

    The glass samples of the Ge-S-I system were synthesized by plasma-enhanced chemical vapor deposition (PECVD) in a low-temperature non-equilibrium RF-plasma discharge. The vapors of S and GeI4 were the initial substances. The process was carried out in a flowing quartz reactor at the walls temperature of 300-500 °C and the total pressure range of 1.9-22.8 Torr. The phase and the elemental compositions of the deposited glassy batches were investigated. The glasses obtained by melting of the solid reaction products were homogenized in the evacuated quartz glass ampoule and they were studied by DSC, X-ray microanalysis, and atomic emission spectroscopy. The proposed method allows to prepare the glasses of the system Ge-S-I with Si content less than 3 ṡ 10-5 wt.%.

  17. Preparation and physico-chemical study of nitroxide radicals. Isotopic marking with carbon 13 and deuterium

    International Nuclear Information System (INIS)

    N-t-butyl-N-phenyl nitroxide is obtained by: a) action of t-butyl-magnesium chloride on nitrobenzene, or of phenyl-magnesium bromide on nitro-t-butane, b) oxidation of N-t-butyl-N-phenylhydroxylamine, c) oxidation of N-t-butylaniline. In these latter two cases, it has been possible to isolate the pure radical and to study it using UV, IR and EPR. It decomposes to give N-t-butylaniline and the N-oxide of N-t-butyl-p-quinon-imine. The action of peracids such as p-nitro-perbenzoic or m-chloro-perbenzoic acids on amines or hydroxylamines leads to the formation of stable or unstable nitroxide radicals easily observable by EPR. Finally, with a view to obtaining definite values for the coupling between the free electron of a nitroxide and carbon 13, the preparation of such radicals marked with 13C in the α or β position of the nitroxide function has been carried out. The coupling with an α carbon 13 is negative and does not appear to vary with the spin density on the nitrogen. The interaction with the p nuclei of the nitrogen depends on the nature of the substituents: the two benzyl protons have a hyperfine splitting aH which is always less than that of the ethyl. On the other hand, the 13C coupling is greater in the first case. The usually adopted conformations for the compounds having the carbonyl group cannot account for the observed values of the β couplings. (author)

  18. Effect of protic solvents on CdS thin films prepared by chemical bath deposition

    International Nuclear Information System (INIS)

    In this study, cadmium sulfide (CdS) thin films are grown on glass substrates by chemical bath deposition (CBD) in an aqueous bath containing 10–20 vol.% alcohol. The roles of ethanol as a protic solvent that substantially improves the quality of films are explored extensively. The deposited films in an alcohol bath are found to be more compact and smoother with smaller CdS grains. The X-ray diffractograms of the samples confirm that all films were polycrystalline with mixed wurtzite (hexagonal) and zinkblende (cubic) phases. Raman spectra indicate that, for a film deposited in an alcohol bath, the position of 1LO is closer to the value for single crystal CdS, indicating that these films have a high degree of crystallinity. The as-deposited CdS thin films in a 10 vol.% alcohol bath were found to have the highest visible transmittance of 81.9%. XPS analysis reveals a stronger signal of C1s for samples deposited in the alcohol baths, indicating that there are more carbonaceous residues on the films with protic solvent than on the films with water. A higher XPS S/Cd atomic ratio for films deposited in an alcohol bath indicates that undesirable surface reactions (leading to sulfur containing compounds other than CdS) occur less frequently over the substrates. - Highlights: • Study of CBD-CdS films grown in an alcohol-containing aqueous bath is reported. • The deposited films in an alcohol bath are more compact with smaller CdS grains. • Raman spectra show that in an alcohol bath, the CdS film has a better crystallinity. • XPS reveals more carbon residues remain on the films deposited using alcohol bath. • In an alcohol bath, the undesirable surface reactions with Cd ions were hindered

  19. The preparation and cathodoluminescence of ZnS nanowires grown by chemical vapor deposition

    International Nuclear Information System (INIS)

    Highlights: ► ZnS nanowires have been achieved by thermal evaporation. ► The nanowires were 20–50 nm in diameter and up to tens of nanometers in length. ► Single-crystalline wurtzite and sphalerite ZnS phase are coexist in the nanowires. ► The ZnS nanowires showed almost identical blue luminescence at room temperature. ► ZnS nanowires may be appropriate for use in UV/blue LED phosphor materials. - Abstract: Single crystal ZnS nanowires were successfully synthesized in large quantities on Si (1 0 0) substrates by simple thermal chemical vapor deposition without using any catalyst. The morphology, composition, and crystal structure were characterized by field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), energy-dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS), and cathodoluminescence (CL) spectroscopy. SEM observations show that the nanowires have diameters about 20–50 nm and lengths up to several tens of micrometers. XRD and TEM results confirmed that the nanowires exhibited both wurtzite and zinc blende structures with growth directions aligned along [0 0 0 2] and [1 1 1], respectively. The CL spectrum revealed emission bands in the UV and blue regions. The blue emissions at 449 and ∼581 nm were attributed to surface states and impurity-related defects of the nanowires, respectively. The perfect crystal structure of the nanowires indicates their potential applications in nanotechnology and in the fabrication of nanodevices.

  20. (001) Oriented piezoelectric films prepared by chemical solution deposition on Ni foils

    International Nuclear Information System (INIS)

    Flexible metal foil substrates are useful in some microelectromechanical systems applications including wearable piezoelectric sensors or energy harvesters based on Pb(Zr,Ti)O3 (PZT) thin films. Full utilization of the potential of piezoelectrics on metal foils requires control of the film crystallographic texture. In this study, (001) oriented PZT thin films were grown by chemical solution deposition (CSD) on Ni foil and Si substrates. Ni foils were passivated using HfO2 grown by atomic layer deposition in order to suppress substrate oxidation during subsequent thermal treatment. To obtain the desired orientation of PZT film, strongly (100) oriented LaNiO3 films were integrated by CSD on the HfO2 coated substrates. A high level of (001) LaNiO3 and PZT film orientation were confirmed by X-ray diffraction patterns. Before poling, the low field dielectric permittivity and loss tangents of (001) oriented PZT films on Ni are near 780 and 0.04 at 1 kHz; the permittivity drops significantly on poling due to in-plane to out-of-plane domain switching. (001) oriented PZT film on Ni displayed a well-saturated hysteresis loop with a large remanent polarization ∼36 μC/cm2, while (100) oriented PZT on Si showed slanted P-E hysteresis loops with much lower remanent polarizations. The |e31,f| piezoelectric coefficient was around 10.6 C/m2 for hot-poled (001) oriented PZT film on Ni.

  1. Evaluation of the effect of conventionally prepared swarna makshika bhasma on different bio-chemical parameters in experimental animals

    Directory of Open Access Journals (Sweden)

    Sudhaldev Mohapatra

    2011-01-01

    Full Text Available Swarna makshika (chalcopyrite bhasma (SMB has been used for different therapeutic purposes since long in Ayurveda. The present study is conducted to evaluate the effect of conventionally prepared SMB on different bio-chemical parameters in experimental animals, for providing scientific data base for its logical use in clinical practice. The genuine SMB was prepared by following classical techniques of shodhana and marana most commonly used by different Ayurvedic drug manufacturers. Shodhana was done by roasting raw swarna makshika with lemon juice for three days and marana was performed by 11 putas . The experimental animals (rats were divided into two groups. SMB mixed with diluted honey was administered orally in therapeutic dose to Group SMB and diluted honey only was administered to vehicle control Group, for 30 days. The blood samples were collected twice, after 15 days and after 30 days of drug administration and different biochemical investigations were done. Biochemical parameters were chosen based on references from Ayurvedic classics and contemporary medicine. It was observed that Hb% was found significantly increased and LDL and VLDL were found significantly decreased in Group SMB when compared with vehicle control group. This experimental data will help the clinician for the logical use of SMB in different disease conditions with findings like low Hb% and high LDL, VLDL levels.

  2. The preparation and chemical reaction kinetics of tungsten bronze thin films and nitrobenzene with and without a catalyst

    Science.gov (United States)

    Materer, Nicholas F.; Apblett, Allen; Kadossov, Evgueni B.; Khan, Kashif Rashid; Casper, Walter; Hays, Kevin; Shams, Eman F.

    2016-06-01

    Microcrystalline tungsten bronze thin films were prepared using wet chemical techniques to reduce a tungsten oxide thin film that was prepared by thermal oxidation of a sputter deposited tungsten metal film on a quartz substrate. The crystallinity of these films was determined by X-ray diffraction and the surface was characterized by X-ray and Ultra-Violet Photoelectron spectroscopy. The total amount of hydrogen incorporated in the film was monitored using absorbance spectroscopy at 900 nm. The oxidation kinetics of the film and the hydrogenation of nitrobenzene in hexane were measured as a function of film thickness. A satisfactory fit of the resulting kinetics was obtained using a model that involves two simultaneous processes. The first one is the proton diffusion from the bulk of the film to the surface, and the second is a reaction of the surface protons with the oxidants. Finally, the dependence of the reaction rates on the presence of catalytic amounts of first row transition metals on the surface of the film was explored.

  3. Studies on Hall Effect and DC Conductivity Measurements of Semiconductor Thin films Prepared by Chemical Bath Deposition (CBD method

    Directory of Open Access Journals (Sweden)

    S. Thirumavalavana

    2015-12-01

    Full Text Available Semiconductors have various useful properties that can be exploited for the realization of a large number of high performance devices in fields such as electronics and optoelectronics. Many novel semiconductors, especially in the form of thin films, are continually being developed. Thin films have drawn the attention of many researchers because of their numerous applications. As the film becomes thinner, the properties acquire greater importance in the miniaturization of elements such as resistors, transistors, capacitors, and solar cells. In the present work, copper selenide (CuSe, cadmium selenide (CdSe, zinc selenide (ZnSe, lead sulphide (PbS, zinc sulphide (ZnS, and cadmium sulphide (CdS thin films were prepared by chemical bath deposition (CBD method. The prepared thin films were analyzed by using Hall measurements in Van Der Pauw configuration (ECOPIA HMS-3000 at room temperature. The Hall parameters such as Hall mobility of the material, resistivity, carrier concentration, Hall coefficient and conductivity were determined. The DC electrical conductivity measurements were also carried out for the thin films using the conventional two – probe technique. The activation energies were also calculated from DC conductivity studies.

  4. Superconducting MgB2 film prepared by chemical vapor deposition at atmospheric pressure of N2

    International Nuclear Information System (INIS)

    A simple and effective chemical vapor deposition equipment was developed for deposition of superconducting MgB2 thin films. The pure precursor Boron films were prepared in base pressure of low vacuum and deposited in atmospheric pressure. After the precursor film annealed in Mg vapor, the superconducting MgB2 film was fabricated. During the precursor Boron films preparation, N2 and Ar were used as carrier gas. Compared to Ar gas, the films show better crystallization, surface morphology and superconducting performance when N2 is adopted as carrier gas. With flow rate of 200 sccm of N2 gas, the fabricated MgB2 films exhibit the highest superconducting transition temperature of 39.5 K, which is among the best results of MgB2 thin films. This method provides a suitable method to realize high quality MgB2 Josephson junctions and industrial manufacture of MgB2 superconducting thin films on a large scale. - Highlights: • Boron films were deposited in atmospheric pressure. • Boron films deposited in N2 atmosphere have better morphology than that of in Ar. • MgB2 films show better crystallization and superconductivity in N2 atmosphere

  5. Conduction mechanism in low-resistivity n-type ZnSe prepared by organometallic chemical vapor deposition

    Science.gov (United States)

    Stutius, W.

    1982-01-01

    n-type ZnSe layers with a room-temperature resistivity of less than 0.05 Ω cm and mobilities of ˜400 cm2/(V sec) have been grown on (100) GaAs by organometallic chemical vapor deposition (OM-CVD), using triethylaluminum as a dopant. No further treatment after the layer growth is necessary in order to achieve the high electrical conductivity. An analysis of the low-temperature electrical transport data and of the photoluminescence data, however, suggests that the physical properties of the layers differ from those of ZnSe prepared by other methods. Charge transport occurs via impurity-band conduction in the more heavily doped layers and via thermally activated hopping in the more lightly doped layers rather than via thermally activated extrinsic conductivity. The degree of compensation of donors is larger than 0.5. The exact nature of the compensating centers in the material prepared by OM-CVD is uncertain at this point, although the photoluminescence data suggest the presence of Al-VZn complexes.

  6. NOVEL PREPARATION AND MAGNETO CHEMICAL CHARACTERIZATION OF NANO-PARTICLE MIXED ALCOHOL CATALYSTS

    Energy Technology Data Exchange (ETDEWEB)

    Seetala V. Naidu; Upali Siriwardane

    2005-01-14

    We have developed effective nanoparticle incorporated heterogeneous F-T catalysts starting with the synthesis of Fe, Co, Cu nanoparticles using Fe(acac){sub 3}, Co(acac){sub 2}, and Cu(acac){sub 2} precursors and incorporating the nanoparticles into alumina sol-gel to yield higher alkanes production. SEM/EDX, XRD, BET, VSM and SQUID experimental techniques were used to characterize the catalysts, and GC/MS were used for catalytic product analysis. The nanoparticle oxide method gave the highest metal loading. In case of mixed metals it seems that Co or Cu interferes and reduces Fe metal loading. The XRD pattern for nanoparticle mixed metal oxides show alloy formation between cobalt and iron, and between copper and iron in sol-gel prepared alumina granules. The alloy formation is also supported by DTA and VMS data. The magnetization studies were used to estimate the catalyst activity in pre- and post-catalysts. A lower limit of {approx}40% for the reduction efficiency was obtained due to hydrogenation at 450 C for 4 hrs. About 85% of the catalyst has become inactive after 25 hrs of catalytic reaction, probably by forming carbides of Fe and Co. The low temperature (300 K to 4.2 K) SQUID magnetometer results indicate a superparamagnetic character of metal nanoparticles with a wide size distribution of < 20 nm nanoparticles. We have developed an efficient and economical procedure for analyzing the F-T products using low cost GC-TCD system with hydrogen as a carrier gas. Two GC columns DC 200/500 and Supelco Carboxen-1000 column were tested for the separation of higher alkanes and the non-condensable gases. The Co/Fe on alumina sol-gel catalyst showed the highest yield for methane among Fe, Co, Cu, Co/Fe, Cu/Co, Fe/Cu. The optimization of CO/H{sub 2} ratio indicated that 1:1 ratio gave more alkanes distribution in F-T process with Co/Fe (6% each) impregnated on alumina mesoporous catalyst.

  7. CHEMICALS

    CERN Multimedia

    Medical Service

    2002-01-01

    It is reminded that all persons who use chemicals must inform CERN's Chemistry Service (TIS-GS-GC) and the CERN Medical Service (TIS-ME). Information concerning their toxicity or other hazards as well as the necessary individual and collective protection measures will be provided by these two services. Users must be in possession of a material safety data sheet (MSDS) for each chemical used. These can be obtained by one of several means : the manufacturer of the chemical (legally obliged to supply an MSDS for each chemical delivered) ; CERN's Chemistry Service of the General Safety Group of TIS ; for chemicals and gases available in the CERN Stores the MSDS has been made available via EDH either in pdf format or else via a link to the supplier's web site. Training courses in chemical safety are available for registration via HR-TD. CERN Medical Service : TIS-ME :73186 or service.medical@cern.ch Chemistry Service : TIS-GS-GC : 78546

  8. Preparation of Fe-doped colloidal SiO(2) abrasives and their chemical mechanical polishing behavior on sapphire substrates.

    Science.gov (United States)

    Lei, Hong; Gu, Qian; Chen, Ruling; Wang, Zhanyong

    2015-08-20

    Abrasives are one of key influencing factors on surface quality during chemical mechanical polishing (CMP). Silica sol, a widely used abrasive in CMP slurries for sapphire substrates, often causes lower material removal rate (MRRs). In the present paper, Fe-doped colloidal SiO2 composite abrasives were prepared by a seed-induced growth method in order to improve the MRR of sapphire substrates. The CMP performance of Fe-doped colloidal SiO2 abrasives on sapphire substrates was investigated using UNIPOL-1502 CMP equipment. Experimental results indicate that the Fe-doped colloidal SiO2 composite abrasives exhibit lower surface roughness and higher MRR than pure colloidal SiO2 abrasives for sapphire substrates under the same testing conditions. Furthermore, the acting mechanism of Fe-doped colloidal SiO2 composite abrasives in sapphire CMP was analyzed by x-ray photoelectron spectroscopy. Analytical results show that the Fe in the composite abrasives can react with the sapphire substrates to form aluminum ferrite (AlFeO3) during CMP, which promotes the chemical effect in CMP and leads to improvement of MRR. PMID:26368752

  9. Effect of Gamma Radiation on Microbial load, Chemical and Sensory Properties of Sheesh Tawoq, Prepared Chilled Meal

    International Nuclear Information System (INIS)

    Locally prepared meal Sheesh Tawoq was treated with 0, 2, 4 or 6 kGy doses of gamma irradiation. Treated and untreated Sheesh Tawoq were kept in a refrigerator (1 and 4 mC). Microbiological, chemical and sensory characteristics of Sheesh Tawoq were evaluated at 0, 4, 8, 12, 16 and 20th week of storage. The results indicate that 4 and 6 kGy doses of gamma irradiation decreased the total counts of mesophilic aerobic bacteria, total coliform and yeast. Thus the microbiological shelf-life of Sheesh Tawoq was significantly extended from 12 weeks (control) to more than 20 weeks (samples treated with 4 or 6 kGy). Irradiation doses did not have a significant effect on the major constituents of Sheesh Tawoq (moisture, protein and fats). The radiation doses required to reduce the microorganisms load one log cycle (D10 ) in Sheesh Tawoq were 435 and 385 Gy for the Salmonella and E. coli , respectively. The chemical parameters, total acidity and volatile basic nitrogen, which were chosen as the indices of freshness, were all well within the acceptable limit for up to 12 weeks for Sheesh Tawoq treated with 0 and 2 kGy, and for up to 20 weeks at 1 and 4 mC for samples treated with 4 and 6 kGy. Sensory evaluation showed no significant differences between irradiated and non-irradiated samples. (author)

  10. Wet Chemical Preparation of Nanoparticles ZnO:Eu3+ and ZnO:Tb3+ with Enhanced Photoluminescence

    Directory of Open Access Journals (Sweden)

    Tran Kim Anh

    2014-01-01

    Full Text Available ZnO doped with Eu3+ and Tb3+ had been successfully prepared by wet chemical method with the assistance of microwave. The influence of reaction conditions such as temperature, time, content of Eu3+, Tb3+ ion, and annealing treatment on the structure and luminescent characteristics was studied. The analysis of energy dispersive spectroscopy (EDS and photoluminescence spectra measurements indicated that Eu3+ and Tb3+ exist in host lattice and create the new emission region compared to ZnO crystalline host lattice. The field emission scanning electron microscope (FE-SEM studies show the Eu3+, Tb3+ doped ZnO nanoparticles have a pseudohexagonal shape. The particle size was 30–50 nm for ZnO:Eu3+ and 40–60 nm for ZnO:Tb3+. Photoluminescence excitation (PLE and photoluminescence (PL spectra at room temperature have been studied to recognize active centers for characteristic luminescence of ZnO:Eu3+ and ZnO:Tb3+. The characteristic luminescent lines of Eu3+ (5D0-7Fj and Tb3+ (5D4-7Fj were determined. It has been demonstrated that the wet chemical synthesis method with microwave assistance can strongly enhance the luminescent intensity of nanoparticles ZnO:Eu3+ in red and ZnO:Tb3+ in green.

  11. Effects of Thermal Annealing on the Optical Properties of Titanium Oxide Thin Films Prepared by Chemical Bath Deposition Technique

    Directory of Open Access Journals (Sweden)

    H.U. Igwe

    2010-08-01

    Full Text Available A titanium oxide thin film was prepared by chemical bath deposition technique, deposited on glass substrates using TiO2 and NaOH solution with triethanolamine (TEA as the complexing agent. The films w ere subjected to post deposition annealing under various temperatures, 100, 150, 200, 300 and 399ºC. The thermal treatment streamlined the properties of the oxide films. The films are transparent in the entire regions of the electromagnetic spectrum, firmly adhered to the substrate and resistant to chemicals. The transmittance is between 20 and 95% while the reflectance is between 0.95 and 1%. The band gaps obtained under various thermal treatments are between 2.50 and 3.0 ev. The refractive index is between 1.52 and 2.55. The thickness achieved is in the range of 0.12-0.14 :m.These properties of the oxide film make it suitable for application in solar cells: Liquid and solid dye-sensitized photoelectrochemical solar cells, photo induced water splitting, dye synthesized solar cells, environmental purifications, gas sensors, display devices, batteries, as well as, solar cells with an organic or inorganic extremely thin absorber. These thin films are also of interest for the photooxidation of water, photocatalysis, electro chromic devices and other uses.

  12. Preparation and characteristics of chemical bath deposited ZnS thin films: Effects of different complexing agents

    Energy Technology Data Exchange (ETDEWEB)

    Shin, Seung Wook [Department of Materials Science and Engineering, KAIST, Daejeon 305-701 (Korea, Republic of); Agawane, G.L.; Gang, Myeng Gil [Photonics Technology Research Institute, Department of Materials Science Engineering, Chonnam National University, Gwangju 500-757 (Korea, Republic of); Moholkar, A.V. [Department of Physics, Shivaji University, Kolhapur 416-004 (India); Moon, Jong-Ha [Photonics Technology Research Institute, Department of Materials Science Engineering, Chonnam National University, Gwangju 500-757 (Korea, Republic of); Kim, Jin Hyeok, E-mail: jinhyeok@chonnam.ac.kr [Photonics Technology Research Institute, Department of Materials Science Engineering, Chonnam National University, Gwangju 500-757 (Korea, Republic of); Lee, Jeong Yong, E-mail: j.y.lee@kaist.ac.kr [Department of Materials Science and Engineering, KAIST, Daejeon 305-701 (Korea, Republic of)

    2012-06-15

    Highlights: Black-Right-Pointing-Pointer Thick ZnS thin films were successfully prepared by chemical bath deposition in a basic medium using less toxic complexing agents. Black-Right-Pointing-Pointer Effect of different complexing agents such as no complexing agent, Na{sub 3}-citrate and a mixture of Na{sub 3}-citrate and EDTA on the properties of ZnS thin films was investigated. Black-Right-Pointing-Pointer ZnS thin film deposited using two complexing agent showed the outstanding characteristics as compared to those using no and one complexing agent. - Abstract: Zinc sulfide (ZnS) thin films were prepared on glass substrates by a chemical bath deposition technique using aqueous zinc acetate and thiourea solutions in a basic medium (pH {approx} 10) at 80 Degree-Sign C. The effects of different complexing agents, such as a non-complexing agent, Na{sub 3}-citrate, and a mixture of Na{sub 3}-citrate and ethylenediamine tetra-acetate (EDTA), on the structural, chemical, morphological, optical, and electrical properties of ZnS thin films were investigated. X-ray diffraction pattern showed that the ZnS thin film deposited without any complexing agent was grown on an amorphous phase. However, the ZnS thin films deposited with one or two complexing agents showed a polycrystalline hexagonal structure. No secondary phase (ZnO) was observed. X-ray photoelectron spectroscopy showed that all ZnS thin films exhibited both Zn-S and Zn-OH bindings. Field emission scanning electron microscopy (FE-SEM) images showed that ZnS thin films deposited with complexing agents had thicker thicknesses than that deposited without a complexing agent. The electrical resistivity of ZnS thin films was over 10{sup 5} {Omega} cm regardless of complexing agents. The average transmittance of the ZnS thin films deposited without a complexing agent, those with Na{sub 3}-citrate, and those with a mixture of Na{sub 3}-citrate and EDTA was approximately 85%, 65%, and 70%, respectively, while the band gap

  13. Controllable preparation of a nano-hydroxyapatite coating on carbon fibers by electrochemical deposition and chemical treatment.

    Science.gov (United States)

    Wang, Xudong; Zhao, Xueni; Wang, Wanying; Zhang, Jing; Zhang, Li; He, Fuzhen; Yang, Jianjun

    2016-06-01

    A nano-hydroxyapatite (HA) coating with appropriate thickness and morphology similar to that of human bone tissue was directly prepared onto the surfaces of carbon fibers (CFs). A mixed solution of nitric acid, hydrochloric acid, sulfuric acid, and hydrogen peroxide (NHSH) was used in the preparation process. The coating was fabricated by combining NHSH treatment and electrochemical deposition (ECD). NHSH treatment is easy to operate, produces rapid reaction, and highly effective. This method was first used to induce the nucleation and growth of HA crystals on the CF surfaces. Numerous O-containing functional groups, such as hydroxyl (-OH) and carboxyl (-COOH) groups, were grafted onto the CF surfaces by NHSH treatment (NHSH-CFs); as such, the amounts of these groups on the functionalized CFs increased by nearly 8- and 12-fold, respectively, compared with those on untreated CFs. After treatment, the NHSH-CFs not only acquired larger specific surface areas but retained surfaces free from serious corrosion or breakage. Hence, NHSH-CFs are ideal depositional substrates of HA coating during ECD. ECD was successfully used to prepare a nano-rod-like HA coating on the NHSH-CF surfaces. The elemental composition, structure, and morphology of the HA coating were effectively controlled by adjusting various technological parameters, such as the current density, deposition time, and temperature. The average central diameter of HA crystals and the coating density increased with increasing deposition time. The average central diameter of most HA crystals on the NHSH-CFs varied from approximately 60nm to 210nm as the deposition time increased from 60min to 180min. Further studies on a possible deposition mechanism revealed that numerous O-containing functional groups on the NHSH-CF surfaces could associate with electrolyte ions (Ca(2+)) to form special chemical bonds. These bonds can induce HA coating deposition and improve the interfacial bonding strength between the HA coating

  14. D-fructose-6-phosphate aldolase in organic synthesis: cascade chemical-enzymatic preparation of sugar-related polyhydroxylated compounds.

    Science.gov (United States)

    Concia, Alda Lisa; Lozano, Carles; Castillo, José A; Parella, Teodor; Joglar, Jesús; Clapés, Pere

    2009-01-01

    Novel aldol addition reactions of dihydroxyacetone (DHA) and hydroxyacetone (HA) to a variety of aldehydes catalyzed by D-fructose-6-phosphate aldolase (FSA) are presented. In a chemical-enzymatic cascade reaction approach, 1-deoxynojirimycin and 1-deoxymannojirimycin were synthesized starting from (R)- and (S)-3-(N-Cbz-amino)-2-hydroxypropanal, respectively. Furthermore, 1,4-dideoxy-1,4-imino-D-arabinitol and 1,4,5-trideoxy-1,4-imino-D-arabinitol were prepared from N-Cbz-glycinal. 1-Deoxy-D-xylulose was also synthesized by using HA as the donor and either 2-benzyloxyethanal or 2-hydroxyethanal as acceptors. In both cases the enzymatic aldol addition reaction was fully stereoselective, but with 2-hydroxyethanal 17 % of the epimeric product at C2, 1-deoxy-D-erythro-2-pentulose, was observed due to enolization/epimerization during the isolation steps. It was also observed that D-(-)-threose is a good acceptor substrate for FSA, opening new synthetic possibilities for the preparation of important novel complex carbohydrate-related compounds from aldoses. To illustrate this, 1-deoxy-D-ido-hept-2-ulose was obtained stereoselectively by the addition of HA to D-(-)-threose, catalyzed by FSA. It was found that the reaction performance depended strongly on the donor substrate, HA being the one that gave the best conversions to the aldol adduct. The examples presented in this work show the valuable synthetic potential of FSA for the construction of chiral complex polyhydroxylated sugar-type structures. PMID:19222084

  15. Preparation and characterization of the 'research chemical' diphenidine, its pyrrolidine analogue, and their 2,2-diphenylethyl isomers.

    Science.gov (United States)

    Wallach, Jason; Kavanagh, Pierce V; McLaughlin, Gavin; Morris, Noreen; Power, John D; Elliott, Simon P; Mercier, Marion S; Lodge, David; Morris, Hamilton; Dempster, Nicola M; Brandt, Simon D

    2015-05-01

    Substances with the diphenylethylamine nucleus represent a recent addition to the product catalog of dissociative agents sold as 'research chemicals' on the Internet. Diphenidine, i.e. 1-(1,2-diphenylethyl)piperidine (1,2-DEP), is such an example but detailed analytical data are less abundant. The present study describes the synthesis of diphenidine and its most obvious isomer, 1-(2,2-diphenylethyl)piperidine (2,2-DEP), in order to assess the ability to differentiate between them. Preparation and characterization were also extended to the two corresponding pyrrolidine analogues 1-(1,2-diphenylethyl)- and 1-(2,2-diphenylethyl)pyrrolidine, respectively. Analytical characterizations included high-resolution electrospray mass spectrometry (HR-ESI-MS), liquid chromatography ESI-MS/MS, gas chromatography ion trap electron and chemical ionization MS, nuclear magnetic resonance spectroscopy (NMR) and infrared spectroscopy. Differentiation between the two isomeric pairs was possible under GC-(EI/CI)-MS conditions and included the formation of distinct iminium ions, such as m/z 174 for 1,2-DEP and m/z 98 for 2,2-DEP, respectively. The pyrrolidine counterparts demonstrated similar phenomena including the expected mass difference of 14 Da due to the lack of one methylene unit in the ring. Two samples obtained from an Internet vendor provided confirmation that diphenidine was present in both samples, concurring with the product label. Finally, it was confirmed that diphenidine (30 μM) reduced N-methyl-D-aspartate-mediated field excitatory postsynaptic potentials (NMDA-fEPSPs) to a similar extent to that of ketamine (30 μM) when using rat hippocampal slices. The appearance of 1,2- diphenylethylamines appears to reflect the exploration of alternatives to arylcyclohexylamine-type substances, such as methoxetamine, PCP and PCPy-based analogues that also show NMDA receptor activity as demonstrated here for diphenidine. PMID:25044512

  16. Effect of gamma irradiation on the microbial load and chemical and sensory properties of locally prepared fast meals

    International Nuclear Information System (INIS)

    Locally prepared meals (kubba, borak, cheese borak and sheesh tawoq) were treated with 2, 4 or 6 kGy doses of gamma irradiation. Treated and untreated samples were kept in a refrigerator (1-4 deg. C). Microbiological and chemical analyses were performed on each treated sample immediately after processing, and weekly throughout the storage period, which lasted for 3 weeks for kubba, 6 weeks for borak and cheese borak and 20 weeks for sheesh tawoq. Sensory evaluation and proximate analysis were done within one week after irradiation. Results of the proximate analysis of borak, cheese borak and sheesh tawoq showed that the irradiation doses did not have a significant effect on the moisture, protein and fat contents of meals, whereas for kubba, irradiation decreased the moisture, protein and fat contents. The doses of gamma irradiation selected decreased the microorganism load and increased the shelf life of all meals studied. The radiation doses required to reduce Salmonella and Escherichia coli by one log cycle (D10) in borak were 0.46 and 0.51 kGy, in cheese borak 0.30 and 0.50 kGy and for sheesh tawoq 0.44 and 0.39 kGy, respectively. The three chemical parameters, total acidity, lipid peroxide and volatile basic nitrogen, which were chosen as the indices of freshness, were all well within the acceptable limit for up to 3 weeks for kubba, 6 weeks for borak and cheese borak and 20 weeks for sheesh tawoq treated with 6 kGy. Sensory evaluation showed no significant differences between irradiated and non-irradiated samples. (author)

  17. Synthesis and structural characterization of tungsten trioxide nanoplatelet-containing thin films prepared by Aqueous Chemical Growth

    International Nuclear Information System (INIS)

    We report the synthesis of WO3 thin films predominantly made up of nanoplatelets, on transparent plain glass microscope slides, by the low-temperature, soft chemistry method of Aqueous Chemical Growth (ACG). During the heterogeneous growth, by ACG, of WO3 thin films onto these plain glass substrates, nanoplatelet and nanorod-like structures of WO3 were also precipitated out of the Peroxotungstic acid precursor solutions and collected as slurries which were annealed at 500 °C to give ultra-fine powders of WO3. Scanning Electron Microscopy of the thin films and powders showed that nanoplatelets formed had thicknesses generally less than 300 nm and lengths and diameters in the 1–2 μm range. The thin films formed were less than 5 μm thick. Transmission Electron Microscopy (TEM) on one of the thin films confirmed the formation of nanoplatelets as well as nanorod-like structures, while High Resolution TEM alongside X-ray Diffraction and Raman spectroscopy suggested that the WO3 thin film grown on a plain glass microscope slide was monoclinic in crystal structure. While Energy Dispersive X-ray Spectroscopy, Fourier Transform-Infrared Spectroscopy, and Attenuated Total Reflection were used to establish the purity and bond structure of WO3 within the thin film, Selected Area Electron Diffraction gave further evidence of crystallinity within the nanostructures prepared. The potential use of the WO3 nanoplatelet-containing thin films for hydrogen sensing at 300 °C was demonstrated. - Highlights: ► WO3 thin films grown on glass slides by Aqueous Chemical Growth, at 90–95 °C ► Formation of square-nanoplatelets in the thin films is confirmed. ► Raman spectroscopy confirms platelets to be monoclinic in crystal structure. ► Drop-coated thick films of WO3 nanoplatelets on glass, sensed H2 at 300 °C

  18. Characterization of electro-conductive fabrics prepared by in situ chemical and electrochemical polymerization of pyrrole onto polyester fabric

    International Nuclear Information System (INIS)

    Highlights: • Surface resistivity of the fabrics decreased rapidly with an increase in add-on. • Add-on and resistivity were not correlated below a resistivity value of about 200 Ω. • Higher add-on but lower surface roughness resulted in lower surface resistivity. • The voltage–current and voltage–temperature behaviours were found to be non-linear. • Electro-conductive fabric exhibited 98% electromagnetic shielding efficiency. - Abstract: This paper reports a study on electro-conductive fabrics prepared by a combined in situ chemical and electrochemical polymerization of pyrrole. Specific observations are made to establish the roles of add-on and surface roughness on the surface resistivity of the electro-conductive fabrics. The performance characteristics of the fabrics are reported in terms of electrical conductivity, voltage–current and voltage–temperature characteristics and electromagnetic interference (EMI) shielding capability. The surface resistivity of the fabric was found to be as low as 11.79 Ω. The voltage–current profile of the fabric is observed to be non-ohmic as well as the voltage–temperature curve is found to be exponential. The EMI shielding efficiency of the fabric was found to be about 98%

  19. TiO2 based photo-catalysts prepared by chemical vapor infiltration (CVI) on micro-fibrous substrates

    International Nuclear Information System (INIS)

    This thesis deals with micro-fibrous glass substrates functionalized with TiO2. The oxide is deposited as a thin film onto the micro fibres by chemical vapour infiltration (CVI), yielding a photo-catalytic material usable for cleaning polluted air. We studied the relation between the structure of the material and its photo-catalytic efficiency. TiO2 thin films were prepared at low pressure, in a hot-wall CVD reactor, using Ti(O-iPr)4 as a precursor. They were characterized by XRD, SEM, EDX, XPS and BET, and by recording the kinetics of decomposition of varied pollutants in solution (orange G, malic acid, imazapyr) and in air (toluene). The conditions favoring the growth of porous films through a columnar growth mode were established by MOCVD-depositing TiO2 thin films on flat substrates. The subsequent works with micro fibrous thick substrates showed the uniformity of infiltration to be the main factor governing the photo-catalytic efficiency. Operating parameters that optimize infiltration do not yield columnar growth mode. A compromise is necessary. Our photo-catalysts are showing high efficiency comparable, if not higher, to those actually commercialized. These promising results are opening real perspectives for the proposed process. (author)

  20. Synthesis, Structural and Optoelectronic Properties of Nanocrystalline CdSe Thin Films Prepared By Chemical Bath Deposition Route

    Directory of Open Access Journals (Sweden)

    C. P. Nikam

    2015-12-01

    Full Text Available Cadmium Selenide (CdSe thin films were deposited onto glass substrates by simple and low cost chemical bath deposition (CBD technique. Aqueous ammonia was used as a complexing agent for the synthesis of these films. Deposition parameters were optimised and the crystal structure and morphology of the films were characterized by x-ray diffraction (XRD and field emission scanning electron microscopy (FE-SEM, respectively. XRD pattern revealed that the as-prepared CdSe thin films are polycrystalline with hexagonal structure. The average crystallite size of CdSe thin film was found to be in the range of 12-16 nm. FE-SEM image revealed that deposited thin films were consisting of nanocrystalline grains, which were coalesced to form bigger grains that are in cluster form distributed over the substrate surface. Transmission spectra showed high transmittance in the visible region and direct optical band gap energy was found to be a function of deposition time.

  1. The influence of solvents and surfactants on the preparation of copper nanoparticles by a chemical reduction method

    International Nuclear Information System (INIS)

    A chemical reduction method for preparing colloidal copper nanoparticles in water and ethylene glycol (EG) is reported. The obtained copper nanoparticles were characterized by powder x-ray diffraction (XRD), transmission electron microscopy (TEM) and UV-visible spectrophotometry (UV-vis). Surface plasmon resonance peaks immediately after the synthesis appeared at 579 and 551 nm for the colloidal copper in water and EG, respectively. The stability of colloidal copper in EG was longer than that in water. The color of solution in water changed from light-red to black and the nanoparticles mostly precipitated after 22 days, which is attributed to the oxidation of copper nanoparticles in copper oxide (I), as was confirmed by optical absorption measurements. In EG, copper nanoparticles were red and stable even after 2 months. Ascorbic acid plays a role as antioxidant for colloidal copper, due to its ability to scavenge free radicals and reactive oxygen molecules. Polyvinyl pyrrolidone works both as size controller and polymeric capping agent because it hinders the nuclei from aggregation through the polar groups, which strongly absorb the copper particles on the surface with coordination bonds

  2. Characterization of electro-conductive fabrics prepared by in situ chemical and electrochemical polymerization of pyrrole onto polyester fabric

    Energy Technology Data Exchange (ETDEWEB)

    Maiti, Syamal; Das, Dipayan; Sen, Kushal, E-mail: kushal@textile.iitd.ernet.in

    2014-09-15

    Highlights: • Surface resistivity of the fabrics decreased rapidly with an increase in add-on. • Add-on and resistivity were not correlated below a resistivity value of about 200 Ω. • Higher add-on but lower surface roughness resulted in lower surface resistivity. • The voltage–current and voltage–temperature behaviours were found to be non-linear. • Electro-conductive fabric exhibited 98% electromagnetic shielding efficiency. - Abstract: This paper reports a study on electro-conductive fabrics prepared by a combined in situ chemical and electrochemical polymerization of pyrrole. Specific observations are made to establish the roles of add-on and surface roughness on the surface resistivity of the electro-conductive fabrics. The performance characteristics of the fabrics are reported in terms of electrical conductivity, voltage–current and voltage–temperature characteristics and electromagnetic interference (EMI) shielding capability. The surface resistivity of the fabric was found to be as low as 11.79 Ω. The voltage–current profile of the fabric is observed to be non-ohmic as well as the voltage–temperature curve is found to be exponential. The EMI shielding efficiency of the fabric was found to be about 98%.

  3. Preparation of alumina coatings on metallic nickel substrate using a room-temperature wet chemical pretreatment method

    International Nuclear Information System (INIS)

    Research highlights: → We have developed a new wet chemical pretreatment method for nickel surface roughening. → The nickel substrate etched for 3 min at room temperature has a high large surface area. → A crack-free primer coating and a slurry coating have very little tiny crack. → This pretreatment method can obtain well-adhered alumina coating. - Abstract: Electrodeposited nickel substrate was effectively micro-roughened with an acidic bath containing 5 wt% H2SO4 and 10 wt% (NH4)2S2O8 at room temperature. The uniformly roughened surface was then sequentially wash-coated with boehmite sol and alumina slurries. The microstructure and the surface performance of the wash-coat/substrate were investigated by scanning electron microscopy and ultrasonic vibration test. The nickel substrate that was etched for 3 min at room temperature yielded a foam-like roughened surface morphology with a high large surface area. A crack-free primer coating and a slurry coating with very little tiny crack can be prepared by using this convenient, energy-saving, and time-efficient pretreatment method.

  4. In situ high temperature XRD studies of ZnO nanopowder prepared via cost effective ultrasonic mist chemical vapour deposition

    Indian Academy of Sciences (India)

    Preetam Singh; Ashvani Kumar; Ajay Kaushal; Davinder Kaur; Ashish Pandey; R N Goyal

    2008-06-01

    Ultrasonic mist chemical vapour deposition (UM–CVD) system has been developed to prepare ZnO nanopowder. This is a promising method for large area deposition at low temperature inspite of being simple, inexpensive and safe. The particle size, lattice parameters and crystal structure of ZnO nanopowder are characterized by in situ high temperature X-ray diffraction (XRD). Surface morphology of powder was studied using transmission electron microscopy (TEM) and field emission electron microscope (FESEM). The optical properties are observed using UV-visible spectrophotometer. The influence of high temperature vacuum annealing on XRD pattern is systematically studied. Results of high temperature XRD showed prominent 100, 002 and 101 reflections among which 101 is of highest intensity. With increase in temperature, a systematic shift in peak positions towards lower 2 values has been observed, which may be due to change in lattice parameters. Temperature dependence of lattice constants under vacuum shows linear increase in their values. Diffraction patterns obtained from TEM are also in agreement with the XRD data. The synthesized powder exhibited the estimated direct bandgap (g) of 3.43 eV. The optical bandgap calculated from Tauc’s relation and the bandgap calculated from the particle size inferred from XRD were in agreement with each other.

  5. Preparation of Fish Oil Triglyceride by Chemical Catalysis%化学催化制备鱼油三甘酯

    Institute of Scientific and Technical Information of China (English)

    毛治国; 刘明; 张春枝; 张显仁; 徐维锋; 吴文忠

    2012-01-01

    [目的]用化学催化方法制备鱼油三甘酯.[方法]采用酯交换反应,以鱼油乙酯和醋酸三甘酯为原料,制备三甘酯型鱼油,同时研究催化剂种类及用量(基于醋酸三甘酯的质量)、反应温度、物料比(油乙酯和醋酸三甘酯的摩尔比)、反应时间对鱼油三甘酯制备的影响,并通过液相色谱对鱼油三甘酯产物的成分进行定量分析.[结果]制备鱼油三甘酯的最佳条件为:催化剂为甲醇钠,用量为三甘酯质量的3.0%,反应温度为100℃,物料比为鱼油乙酯过量5%(相对于醋酸三甘酯),反应时间为2h.在此最佳条件下制备产物三甘酯含量大于80%.[结论]通过此方法可实现鱼油乙酯向鱼油三甘酯的转化,成本较低,扩大了鱼油类产品在医药和保健品中的应用.%[ Objective] The aim was to prepare fish oil triglyceride by the chemical catalysis method. [ Method] Taking fish oil ethyl ester and glycerol triacetate as raw materials, prepare fish oil triglyceride by transesterification. Then to study the effects of the kind of catalyst and the amount of it (based on the mass of glycerol triacetate) , reaction temperature, mole ratio of fish oil ethyl ester to glycerol triacetate,reaction time on the preparation of fish oil triglyceride. And the composition of the product was analyzed by liquid chromatography quantitatively. [ Result] The optimum conditions of the preparation of fish oil triglyceride were as follows: sodium methoxide was as a catalyst and the amount of it was 3.0% , reaction temperature was 100 t, mole ratio between glycerol triacetate and fish oil ethyl ester was 5% more of fish oil ethyl ester, reaction time was 2 h. Under these conditions, the content of fish oil triglyceride in the product was above 80%. [ Conclusion] This method can be achieved the conversion of fish oil ethyl ester to fish oil triglyceride, and has lower cost, can expand the application of fish oil products in the medicine and health

  6. Possible preparation of wood-plastic composites based on unsaturated polyester resins and styrene by radiation and chemical methods in combination

    International Nuclear Information System (INIS)

    Using the radiation chemical method it is possible to prepare wood-plastic composites using doses of 1 to 2.5 kGy. The impregnation mixture in the wood gelatinates and subsequent curing using chemical initiators takes place without outflow of the mixture from the wood and without formation of incrustations. The basic components of the impregnation mixtures used were unsaturated polyester resins; styrene or methyl methacrylate was used as the thinner. The proven initiator of polymerization was 2,2'-azobisisobutyronitrile. The technology is described of wood impregnation and radiation or chemical curing. The effects were monitored of viscosity, temperature, radiation dose and the concentrations of the individual components of the impregnation mixtures and initiators of polymerization on the process of the preparation of wood-plastic composites. (M.D.)

  7. Chemical approach to solvent removal during nanoencapsulation: its application to preparation of PLGA nanoparticles with non-halogenated solvent

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Youngme [Ewha Womans University, College of Pharmacy (Korea, Republic of); Sah, Eric [University of Notre Dame, College of Science (United States); Sah, Hongkee, E-mail: hsah@ewha.ac.kr [Ewha Womans University, College of Pharmacy (Korea, Republic of)

    2015-11-15

    The objective of this study was to develop a new oil-in-water emulsion-based nanoencapsulation method for the preparation of PLGA nanoparticles using a non-halogenated solvent. PLGA (60–150 mg) was dissolved in 3 ml of methyl propionate, which was vortexed with 4 ml of a 0.5–4 % polyvinyl alcohol solution. This premix was sonicated for 2 min, added into 30 ml of the aqueous polyvinyl alcohol solution, and reacted with 3 ml of 10 N NaOH. Solvent removal was achieved by the alkaline hydrolysis of methyl propionate dissolved in an aqueous phase into water-soluble methanol and sodium propionate. It was a simple but effective technique to quickly harden nanoemulsion droplets into nanoparticles. The appearing PLGA nanoparticles were recovered by ultracentrifugation and/or dialysis, lyophilized with trehalose, and redispersed by water. This nanoencapsulation technique permitted a control of their mean diameters over 151.7 ± 3.8 to 440.2 ± 22.2 nm at mild processing conditions. When the aqueous polyvinyl alcohol concentration was set at ≥1 %, nanoparticles showed uniform distributions with polydispersity indices below 0.1. There were no significant changes in their mean diameters and size distribution patterns before and after lyophilization. When mestranol was encapsulated into nanoparticles, the drug was completely nanoencapsulated: depending on experimental conditions, their encapsulation efficiencies were determined to be 99.4 ± 7.2 to 105.8 ± 6.3 %. This simple, facile nanoencapsulation technique might have versatile applications for the preparation of polymeric nanoparticulate dosage forms.Graphical AbstractSchematic illustration of an innovative chemical approach to solvent removal during nanoencapsulation. Methyl propionate present in the aqueous continuous phase reacts with sodium hydroxide, thereby producing methanol and sodium propionate. Its alkaline hydrolysis allows the continuous extraction of the solvent out of nanoemulsion

  8. Synthesis and characterization of the manganese cobaltite spinel prepared using two 'soft chemical' methods

    Energy Technology Data Exchange (ETDEWEB)

    Brylewski, Tomasz, E-mail: brylew@agh.edu.pl [AGH University of Science and Technology, Faculty of Materials Science and Ceramics, Al. Mickiewicza 30, 30-059 Krakow (Poland); Kruk, Andrzej; Adamczyk, Anna; Kucza, Witold; Stygar, Miroslaw; Przybylski, Kazimierz [AGH University of Science and Technology, Faculty of Materials Science and Ceramics, Al. Mickiewicza 30, 30-059 Krakow (Poland)

    2012-11-15

    Using the coprecipitation method and EDTA gel processes, manganese cobaltite (Mn{sub 1.5}Co{sub 1.5}O{sub 4}) powders were successfully synthesized. The thermal decomposition behavior of the gel precursors, phase formation and morphology of the Mn{sub 1.5}Co{sub 1.5}O{sub 4} powders were characterized by means of DTA/TGA and MS analyses, X-ray diffraction (XRD), and scanning electron microscopy (SEM), respectively. Well-crystallized dual-phase manganese cobaltite spinel, containing both the cubic and tetragonal phases, was obtained at room temperature for both types of powders calcinated at 800 Degree-Sign C for 10 h in static air, without formation of any intermediate phase. SEM investigations show that the Mn{sub 1.5}Co{sub 1.5}O{sub 4} powders prepared using two 'soft chemical' methods were agglomerates composed of approximately micron-sized particles. The structure and morphology of the bulk samples, as well as their electrical conductivity, were investigated using XRD, SEM, and EIS, respectively. Mn{sub 1.5}Co{sub 1.5}O{sub 4} spinels with different microstructure exhibited excellent electrical conductivity and structural stability. Major emphasis was placed on structural transformations of the spinel solid solutions with temperature and their effect on the electrical properties of these solutions. -- Highlights: Black-Right-Pointing-Pointer Mn{sub 1.5}Co{sub 1.5}O{sub 4} powders were prepared using coprecipitation and EDTA gel processes. Black-Right-Pointing-Pointer Approximately micron-sized particles with cubic and tetragonal grains. Black-Right-Pointing-Pointer A transition occurs in the 250-450 Degree-Sign C range. Black-Right-Pointing-Pointer Only the cubic spinel phase is observed at higher temperatures. Black-Right-Pointing-Pointer At higher temperature electrical conductivity is related to the grain volume.

  9. Traditional Aboriginal Preparation Alters the Chemical Profile of Carica papaya Leaves and Impacts on Cytotoxicity towards Human Squamous Cell Carcinoma.

    Science.gov (United States)

    Nguyen, Thao T; Parat, Marie-Odile; Shaw, Paul N; Hewavitharana, Amitha K; Hodson, Mark P

    2016-01-01

    Carica papaya leaf decoction, an Australian Aboriginal remedy, has been used widely for its healing capabilities against cancer, with numerous anecdotal reports. In this study we investigated its in vitro cytotoxicity on human squamous cell carcinoma cells followed by metabolomic profiling of Carica papaya leaf decoction and leaf juice/brewed leaf juice to determine the effects imparted by the long heating process typical of the Aboriginal remedy preparation. MTT assay results showed that in comparison with the decoction, the leaf juice not only exhibited a stronger cytotoxic effect on SCC25 cancer cells, but also produced a significant cancer-selective effect as shown by tests on non-cancerous human keratinocyte HaCaT cells. Furthermore, evidence from testing brewed leaf juice on these two cell lines suggested that the brewing process markedly reduced the selective effect of Carica papaya leaf on SCC25 cancer cells. To tentatively identify the compounds that contribute to the distinct selective anticancer activity of leaf juice, an untargeted metabolomic approach employing Ultra High Performance Liquid Chromatography-Quadrupole Time of Flight-Mass Spectrometry followed by multivariate data analysis was applied. Some 90 and 104 peaks in positive and negative mode respectively were selected as discriminatory features from the chemical profile of leaf juice and >1500 putative compound IDs were obtained via database searching. Direct comparison of chromatographic and tandem mass spectral data to available reference compounds confirmed one feature as a match with its proposed authentic standard, namely pheophorbide A. However, despite pheophorbide A exhibiting cytotoxic activity on SCC25 cancer cells, it did not prove to be the compound contributing principally to the selective activity of leaf juice. With promising results suggesting stronger and more selective anticancer effects when compared to the Aboriginal remedy, Carica papaya leaf juice warrants further study

  10. Electrochromic and colorimetric properties of nickel(II) oxide thin films prepared by aerosol-assisted chemical vapor deposition.

    Science.gov (United States)

    Sialvi, Muhammad Z; Mortimer, Roger J; Wilcox, Geoffrey D; Teridi, Asri Mat; Varley, Thomas S; Wijayantha, K G Upul; Kirk, Caroline A

    2013-06-26

    Aerosol-assisted chemical vapor deposition (AACVD) was used for the first time in the preparation of thin-film electrochromic nickel(II) oxide (NiO). The as-deposited films were cubic NiO, with an octahedral-like grain structure, and an optical band gap that decreased from 3.61 to 3.48 eV on increase in film thickness (in the range 500-1000 nm). On oxidative voltammetric cycling in aqueous KOH (0.1 mol dm(-3)) electrolyte, the morphology gradually changed to an open porous NiO structure. The electrochromic properties of the films were investigated as a function of film thickness, following 50, 100, and 500 conditioning oxidative voltammetric cycles in aqueous KOH (0.1 mol dm(-3)). Light modulation of the films increased with the number of conditioning cycles. The maximum coloration efficiency (CE) for the NiO (transmissive light green, the "bleached" state) to NiOOH (deep brown, the colored state) electrochromic process was found to be 56.3 cm(2) C(-1) (at 450 nm) for films prepared by AACVD for 15 min followed by 100 "bleached"-to-colored conditioning oxidative voltammetric cycles. Electrochromic response times were bleaching process. The films showed good stability when tested for up to 10 000 color/bleach cycles. Using the CIE (Commission Internationale de l'Eclairage) system of colorimetry the color stimuli of the electrochromic NiO films and the changes that take place on reversibly oxidatively switching to the NiOOH form were calculated from in situ visible spectra recorded under electrochemical control. Reversible changes in the hue and saturation occur on oxidation of the NiO (transmissive light green) form to the NiOOH (deep brown) form, as shown by the track of the CIE 1931 xy chromaticity coordinates. As the NiO film is oxidized, a sharp decrease in luminance was observed. CIELAB L*a*b* coordinates were also used to quantify the electrochromic color states. A combination of a low L* and positive a* and b* values quantified the perceived deep brown

  11. Chemical approach to solvent removal during nanoencapsulation: its application to preparation of PLGA nanoparticles with non-halogenated solvent

    International Nuclear Information System (INIS)

    The objective of this study was to develop a new oil-in-water emulsion-based nanoencapsulation method for the preparation of PLGA nanoparticles using a non-halogenated solvent. PLGA (60–150 mg) was dissolved in 3 ml of methyl propionate, which was vortexed with 4 ml of a 0.5–4 % polyvinyl alcohol solution. This premix was sonicated for 2 min, added into 30 ml of the aqueous polyvinyl alcohol solution, and reacted with 3 ml of 10 N NaOH. Solvent removal was achieved by the alkaline hydrolysis of methyl propionate dissolved in an aqueous phase into water-soluble methanol and sodium propionate. It was a simple but effective technique to quickly harden nanoemulsion droplets into nanoparticles. The appearing PLGA nanoparticles were recovered by ultracentrifugation and/or dialysis, lyophilized with trehalose, and redispersed by water. This nanoencapsulation technique permitted a control of their mean diameters over 151.7 ± 3.8 to 440.2 ± 22.2 nm at mild processing conditions. When the aqueous polyvinyl alcohol concentration was set at ≥1 %, nanoparticles showed uniform distributions with polydispersity indices below 0.1. There were no significant changes in their mean diameters and size distribution patterns before and after lyophilization. When mestranol was encapsulated into nanoparticles, the drug was completely nanoencapsulated: depending on experimental conditions, their encapsulation efficiencies were determined to be 99.4 ± 7.2 to 105.8 ± 6.3 %. This simple, facile nanoencapsulation technique might have versatile applications for the preparation of polymeric nanoparticulate dosage forms.Graphical AbstractSchematic illustration of an innovative chemical approach to solvent removal during nanoencapsulation. Methyl propionate present in the aqueous continuous phase reacts with sodium hydroxide, thereby producing methanol and sodium propionate. Its alkaline hydrolysis allows the continuous extraction of the solvent out of nanoemulsion

  12. YBa{sub 2}Cu{sub 3}O{sub 7-x} thin films prepared by chemical solution deposition

    Energy Technology Data Exchange (ETDEWEB)

    Apetrii, Claudia

    2009-11-25

    The discovery of superconductivity in ceramic materials by Bednorz and Mueller in early 1987, immediately followed by Wu et al., who showed that YBa{sub 2}Cu{sub 3}O{sub 7-x} (YBCO) becomes superconducting (92 K) well above the boiling point of nitrogen (77 K) created a great excitement in superconductivity research. Potential applications of high T{sub c}-superconductors require large critical currents and high-applied magnetic fields. Effective ways to increase the critical current density at high magnetic fields in YBCO are the introduction of nanoparticles and chemical substitution of yttrium by other rare earth elements. Since low costs and environmental compatibility are essential conditions for the preparation of long length YBCO films, the cost effective chemical solution deposition (CSD) procedure was selected, given that no vacuum technology is required. To reveal the flexibility and the good optimization possibilities of the CSD approach two main processes were chosen for comparison: a fluorine-free method, namely the polymer-metal precursor technique, and a fluorine-based method, the metalorganic deposition (MOD) using the trifluoroacetates (TFA) technique. Sharp transition temperature widths {delta}T{sub c} of 1.1 K for the polymer metal method, 0.8 K for TFA method and critical current densities J{sub c} of {approx}3.5 MA/cm{sup 2} shows that high quality YBCO thin films can be produced using both techniques. Especially interesting is the magnetic field dependence of the critical current density J{sub c}(B) of the Y(Dy)BCO (80 %) films showing that for the lower magnetic fields the critical current density J{sub c}(B) is higher for a standard YBCO film, but at fields higher than 4.5 T the critical current density J{sub c}(B) of Y(Dy)BCO is larger than that for the YBCO. Above 8 T, J{sub c}(B) of the Y(Dy)BCO film is more than one order of magnitude higher than in pure YBCO film. (orig.)

  13. Adhesion of fibroblasts on micro- and nanostructured surfaces prepared by chemical vapor deposition and pulsed laser treatment

    Energy Technology Data Exchange (ETDEWEB)

    Veith, M; Aktas, O C; Ullah Wazir, H; Grobelsek, I [INM-Leibniz Institute for New Materials, Campus D2 2, 66123 Saarbruecken (Germany); Metzger, W; Sossong, D; Pohlemann, T; Oberringer, M [Department of Trauma-, Hand- and Reconstructive Surgery, Saarland University, Kirrberger Strasse, Building 57, 66421 Homburg (Germany); Puetz, N; Wennemuth, G, E-mail: Michael.Veith@inm-gmbh.d [Department of Anatomy and Cell Biology, Saarland University, Kirrberger Strasse, Building 61, 66421 Homburg (Germany)

    2010-09-15

    The development of micro- and nanostructured surfaces which improve the cell-substrate interaction is of great interest in today's implant applications. In this regard, Al/Al{sub 2}O{sub 3} bi-phasic nanowires were synthesized by chemical vapor deposition of the molecular precursor ({sup t}BuOAlH{sub 2}){sub 2}. Heat treatment of such bi-phasic nanowires with short laser pulses leads to micro- and nanostructured Al{sub 2}O{sub 3} surfaces. Such surfaces were characterized by scanning electron microscopy (SEM), electron dispersive spectroscopy and x-ray photoelectron spectroscopy. Following the detailed material characterization, the prepared surfaces were tested for their cell compatibility using normal human dermal fibroblasts. While the cells cultivated on Al/Al{sub 2}O{sub 3} bi-phasic nanowires showed an unusual morphology, cells cultivated on nanowires treated with one and two laser pulses exhibited morphologies similar to those observed on the control substrate. The highest cell density was observed on surfaces treated with one laser pulse. The interaction of the cells with the nano- and microstructures was investigated by SEM analysis in detail. Laser treatment of Al/Al{sub 2}O{sub 3} bi-phasic nanowires is a fast and easy method to fabricate nano- and microstructured Al{sub 2}O{sub 3}-surfaces for studying cell-surface interactions. It is our goal to develop a biocompatible Al{sub 2}O{sub 3}-surface which could be used as a coating material for medical implants exhibiting a cell selective response because of its specific physical landscape and especially because it promotes the adhesion of osteoblasts while minimizing the adhesion of fibroblasts.

  14. Antimicrobial activity of novel nanostructured Cu-SiO2 coatings prepared by chemical vapour deposition against hospital related pathogens.

    Science.gov (United States)

    Varghese, Sajnu; Elfakhri, Souad O; Sheel, David W; Sheel, Paul; Bolton, Frederick J Eric; Foster, Howard A

    2013-01-01

    There is increasing recognition that the healthcare environment acts as an important reservoir for transmission of healthcare acquired infections (HCAI). One method of reducing environmental contamination would be use of antimicrobial materials. The antimicrobial activity of thin silica-copper films prepared by chemical vapour deposition was evaluated against standard strains of bacteria used for disinfectant testing and bacteria of current interest in HCAI. The structure of the coatings was determined using Scanning Electron Microscopy and their hardness and adhesion to the substrate determined. Antimicrobial activity was tested using a method based on BS ISO 22196:2007. The coatings had a pale green-brown colour and had a similar hardness to steel. SEM showed nano-structured aggregates of Cu within a silica matrix. A log10 reduction in viability of >5 could be obtained within 4 h for the disinfectant test strains and within 6 h for producing Acinetobacter baumannii, Klebsiella pneumoniae and Stenotrophomonas maltophilia. Activity against the other hospital isolates was slower but still gave log10 reduction factors of >5 for extended spectrum β-lactamase producing Escherichia coli and >3 for vancomycin resistant Enterococcus faecium, methicillin resistant Staphylococcus aureus and Pseudomonas aeruginosa within 24 h. The results demonstrate the importance of testing antimicrobial materials destined for healthcare use against isolates of current interest in hospitals as well as standard test strains. The coatings used here can also be applied to substrates such as metals and ceramics and have potential applications where reduction of microbial environmental contamination is desirable. PMID:24007899

  15. Densification and microstructure of carbon/carbon composites prepared by chemical vapor infiltration using ethanol as precursor

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Chemical vapor infiltration of carbon fiber felts with uniform initial bulk density of 0.47 g·cm-3 was investigated at the ethanol partial pressures of 5-20 kPa,as well as the temperatures of 1050,1100,1150 and 1200°C.Ethanol,diluted by nitrogen,was employed as the precursor of pyrolytic carbon.Polarized light microscopy(PLM),scanning electron microscopy and X-ray diffraction were adopted to study the texture of pyrolytic carbon deposited at various temperatures.A change from medium-to high-textured pyrolytic carbon was observed in the sample infiltrated at 1050°C.Whereas,homogeneous high-textured pyrolytic carbons were deposited at the temperatures of 1100,1150 and 1200°C.Extinction angles of 19°-21° were determined for different regions in the samples densified at the temperatures ranging from 1100 to 1200°C.Scanning electron microscopy of the fracture surface after bending test indicated that the prepared carbon/carbon composite samples exhibited a pseudo-plastic fracture behavior.In addition,fracture behavior of the carbon/carbon samples was obviously effected by their infiltration temperature.The fracture mode of C/C composites was transformed from shearing failure to tensile breakage with increasing infiltration temperature. Results of this study show that ethanol is a promising carbon source to synthesize carbon/carbon composites with homogeneously high-textured pyrolytic carbon over a wide range of temperatures(from 1100 to 1200°C).

  16. Storage stability of margarines produced from enzymatically interesterified fats compared to those prepared by conventional methods - Chemical properties

    DEFF Research Database (Denmark)

    Zhang, Hong; Jacobsen, Charlotte; Pedersen, Lars Saaby; Christensen, Morten Wurtz; Adler-Nissen, Jens

    2006-01-01

    selected commercial margarines. The changes in the chemical properties of the products, including peroxide values (PV), tocopherols, free fatty acids, volatile oxidation products, and sensory evaluation, were examined during storage. It was observed that the margarine produced from the chemically...

  17. Aqueous Chemical Solution Deposition of Novel, Thick and Dense Lattice-Matched Single Buffer Layers Suitable for YBCO Coated Conductors: Preparation and Characterization

    OpenAIRE

    Isabel Van Driessche; Petra Lommens; Sigelinde van Steenberge; Vyshnavi Narayanan

    2012-01-01

    In this work we present the preparation and characterization of cerium doped lanthanum zirconate (LCZO) films and non-stoichiometric lanthanum zirconate (LZO) buffer layers on metallic Ni-5% W substrates using chemical solution deposition (CSD), starting from aqueous precursor solutions. La2Zr2O7 films doped with varying percentages of Ce at constant La concentration (La0.5CexZr1−xOy) were prepared as well as non-stoichiometric La0.5+xZr0.5−xOy buffer layers with different percentages of La a...

  18. Annealing effects on zinc oxide-silica films prepared by sol–gel technique for chemical sensing applications

    Energy Technology Data Exchange (ETDEWEB)

    Ali, Atif Mossad, E-mail: atifali@kku.edu.sa [Department of Physics, Faculty of Science, King Khalid University, Abha (Saudi Arabia); Department of Physics, Faculty of Science, Assiut University, Assiut 71516 (Egypt); Ismail, Adel A. [Promising Centre for Sensors and Electronic Devices (PCSED), Najran University, PO Box 1988, Najran 11001 (Saudi Arabia); Central Metallurgical R and D Institute, CMRDI, Helwan, Cairo 11421 (Egypt); Najmy, Rasha [Science Department, Girls' College of Education, King Khalid University (Saudi Arabia); Al-Hajry, Ali [Promising Centre for Sensors and Electronic Devices (PCSED), Najran University, PO Box 1988, Najran 11001 (Saudi Arabia); Department of Physics, College of Science and Arts, Najran University (Saudi Arabia)

    2014-05-02

    ZnO:SiO{sub 2} films are prepared by sol–gel technique on Si substrates. The effect of annealing temperatures (T{sub a}) on the structure, surface morphology, and optical and photoluminescence (PL) properties of these films is studied. The X-ray diffraction analysis revealed that the c-axis orientation and the grain size of ZnO:SiO{sub 2} films increased at high T{sub a}. High-resolution transmission electron microscopy results showed that the ZnO nanoparticles are spherical in shape with their size increasing from 5 to 15 nm with T{sub a} while PL spectroscopy showed few separated PL bands. In addition, two optical band gaps located at 3.0 eV and 4.2 eV are observed and showed a redshift with T{sub a} up to 600 °C, and then a blueshift is observed at 800 °C. ZnO:SiO{sub 2} film was tested as sensors for the detection and quantification of phenyl hydrazine. It is found that ZnO:SiO{sub 2} films showed good sensitivity of 390 μA mM{sup −1} cm{sup −2} and a lower limit of detection of 3 mM with linear dynamic range of 0.05 mM to 3 mM and rapid reaction kinetics (in the order of seconds). The cycling tests indicated that the ZnO:SiO{sub 2} films are quite stable since no significant decrease in sensitivity was observed even after being used repetitively for 3 times, showing a good potential for practical applications. - Highlights: • The nanoparticles size increased from 5 to 15 nm with the annealing temperatures. • Two optical band gaps located at 3.0 eV and 4.2 eV are observed. • ZnO:SiO{sub 2} showed good sensitivity and lower limit of detection. • Cycling test indicated ZnO:SiO{sub 2} was stable during liquid–solid chemical sensing.

  19. Annealing effects on zinc oxide-silica films prepared by sol–gel technique for chemical sensing applications

    International Nuclear Information System (INIS)

    ZnO:SiO2 films are prepared by sol–gel technique on Si substrates. The effect of annealing temperatures (Ta) on the structure, surface morphology, and optical and photoluminescence (PL) properties of these films is studied. The X-ray diffraction analysis revealed that the c-axis orientation and the grain size of ZnO:SiO2 films increased at high Ta. High-resolution transmission electron microscopy results showed that the ZnO nanoparticles are spherical in shape with their size increasing from 5 to 15 nm with Ta while PL spectroscopy showed few separated PL bands. In addition, two optical band gaps located at 3.0 eV and 4.2 eV are observed and showed a redshift with Ta up to 600 °C, and then a blueshift is observed at 800 °C. ZnO:SiO2 film was tested as sensors for the detection and quantification of phenyl hydrazine. It is found that ZnO:SiO2 films showed good sensitivity of 390 μA mM−1 cm−2 and a lower limit of detection of 3 mM with linear dynamic range of 0.05 mM to 3 mM and rapid reaction kinetics (in the order of seconds). The cycling tests indicated that the ZnO:SiO2 films are quite stable since no significant decrease in sensitivity was observed even after being used repetitively for 3 times, showing a good potential for practical applications. - Highlights: • The nanoparticles size increased from 5 to 15 nm with the annealing temperatures. • Two optical band gaps located at 3.0 eV and 4.2 eV are observed. • ZnO:SiO2 showed good sensitivity and lower limit of detection. • Cycling test indicated ZnO:SiO2 was stable during liquid–solid chemical sensing

  20. Preparation, Biodegradation of Coconut Oil Driven Chemically Modified Bovine Serum Albumin Microparticles of Encapsulated Cicer arietinum Amylase and Study of Their Application in Washing Detergents

    OpenAIRE

    Kirti Rani; Vartika Mehta

    2014-01-01

    In present work, Cicer arietinum amylase was encapsulated by emulsification through covalent coupling by glutaraldehyde into chemically modified bovine serum albumin. Biodegradation of coconut oil driven emulsified bovine serum albumin encapsulated Cicer arietinum amylase was carried out by the alkaline protease for its controlled and sustained release of encapsulated enzyme from prepared microparticles of encapsulated Cicer arietinum amylase and its stability increased up to 6 months as comp...

  1. Preparation of nanostructured nickel aluminate spinel powder from spent NiO/Al2O3 catalyst by mechano-chemical synthesis

    OpenAIRE

    Nazemi, M.K.; Sheibani, S; Rashchi, F; González-Delacruz, V.M.; Caballero, Alfonso

    2012-01-01

    In this paper, the possibility of mechano-chemical synthesis, as a single step process for preparation of nanostructured nickel aluminate spinel powder from NiO/Al2O3 spent catalyst was investigated. Powder samples were characterized in terms of composition, morphology, structure, particle size and surface area using complementary techniques such as X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), differential thermal analysis (DTA) and volu...

  2. Possible preparation of wood-plastic materials based on unsaturated polyester resins and methyl metacrylate, by radiation and chemical methods in combination

    International Nuclear Information System (INIS)

    The preparation of wood-plastic combinations (WPC) using combined methods for curing intermediate products and final products is described. In the first step, impregnated wood was irradiated using doses of 1 to 10 kGy in the presence of chemical initiators of polymerization. Thereafter, curing of this partly cured impregnating mixture was accomplished in the wood at elevated temperatures with the aid of chemical initiators of polymerization. Impregnation mixtures based on unsaturated polyester resins and methyl methacrylate, and the wood species European Beech (Fagus silvatica) and Black Alder (Alnus glutinosa) were used. The results indicate that this method of preparing WPC allows substantially lower radiation doses to be used, i.e., doses in the range of 1 to 2.5 kGy. These doses gelatinate the impregnation mixture in the wood so that the subsequent curing by chemical polymerization initiators proceeds without the impregnation mixture flowing out of the wood, and without forming bosses and incrustations. Intermediate products and wood products needing no further finish may thus be prepared: in some cases regrinding or repolish is sufficient. The possibility of using impregnation mixtures based on various unsaturated polyester resins was investigated, and the influence on the curing process of temperature, polymerization initiator concentration, methyl methacrylate concentration, inhibitor concentration, and other factors affecting curing was evaluated. (author)

  3. Influence of the preparation procedure on the chemical and microstructural properties of lanthana promoted Rh/SiO{sub 2} catalysts. A FTIR spectroscopic study of chemisorbed CO

    Energy Technology Data Exchange (ETDEWEB)

    Bernal, S. [Cadiz Univ. (Spain). Facultad de Ciencias; Blanco, G. [Cadiz Univ. (Spain). Facultad de Ciencias; Calvino, J.J. [Cadiz Univ. (Spain). Facultad de Ciencias; Cauqui, M.A. [Cadiz Univ. (Spain). Facultad de Ciencias; Rodriguez-Izquierdo, J.M. [Cadiz Univ. (Spain). Facultad de Ciencias; Vidal, H. [Cadiz Univ. (Spain). Facultad de Ciencias

    1997-03-20

    In this work, the influence of the preparation procedure on the chemical and microstructural properties of a series of Rh/La{sub 2}O{sub 3}/SiO{sub 2} catalysts has been investigated. The catalysts were characterized by using HREM, H{sub 2} and CO volumetric adsorption and FTIR spectroscopy of chemisorbed CO. From our study, significant effects were observed for the following preparative variables: (a) the lanthana loading; (b) the way of introducing the metal and promoter, either consecutive (lanthana first and then the rhodium salt) or by co-impregnation; and (c) the calcination temperature (873 K or 1173 K) applied for preparing the La{sub 2}O{sub 3}/SiO{sub 2} intermediate phase onto which the noble metal was deposited. (orig.)

  4. Sol-gel process preparation and evaluation of the analytical performances of an hydrazine specific chemical sensor

    International Nuclear Information System (INIS)

    The realisation of optical fibers active chemical collector to analyze hydrazine in line, in the spent fuel reprocessing process is the subject of this work. The p.dimethyl-amino-benzaldehyde has been chosen as reagent for its chemical and optical properties

  5. Combining Chemical Information Literacy, Communication Skills, Career Preparation, Ethics, and Peer Review in a Team-Taught Chemistry Course

    Science.gov (United States)

    Jones, Mary Lou Baker; Seybold, Paul G.

    2016-01-01

    The widely acknowledged need to include chemical information competencies and communication skills in the undergraduate chemistry curriculum can be accommodated in a variety of ways. We describe a team-taught, semester-length course at Wright State University which combines chemical information literacy, written and oral communication skills,…

  6. Preparation of LWBR [Light Water Breeder Reactor] spent fuel for shipment to ICPP [Idaho Chemical Processing Plant] for long term storage (LWBR Development Program)

    International Nuclear Information System (INIS)

    After successfully operating for 29,047 effective full power hours, the Light Water Breeder Reactor (LWBR) core was defueled prior to total decommissioning of the Shippingport facility. All nuclear fuel and much of the reactor internal hardware was removed from the reactor vessel. Non-fuel components were prepared for shipment to disposal sites, and the fuel assemblies were partially disassembled and shipped to the Expended Core Facility (ECF) in Idaho. At ECF, the fuel modules underwent further disassembly to provide fuel rods for nondestructive testing to establish the core's breeding efficiency and to provide core components for examinations to assess their performance characteristics. This report presents a basic description of the processes and equipment used to prepare and to ship all LWBR nuclear fuel to the Idaho Chemical Processing Plant (ICPP) for long-term storage. Preparation processes included the underwater loading of LWBR fuel into storage liners, the sealing, dewatering and drying of the storage liners, and the final pressurization of the storage liners with inert neon gas. Shipping operations included the underwater installation of the fuel loaded storage liner into the Peach Bottom shipping cask, cask removal from the waterpit, cask preparations for shipping, and cask shipment by tractor trailer to the ICPP facility for long-term storage. The ICPP facility preparations for LWBR fuel storage and the ICPP process for discharge of the fuel into underground silos are presented. 10 refs., 42 figs

  7. Three-dimensional assemblies of graphene prepared by a novel chemical reduction-induced self-assembly method

    KAUST Repository

    Zhang, Lianbin

    2012-01-01

    In this study, three-dimensional (3D) graphene assemblies are prepared from graphene oxide (GO) by a facile in situ reduction-assembly method, using a novel, low-cost, and environment-friendly reducing medium which is a combination of oxalic acid (OA) and sodium iodide (NaI). It is demonstrated that the combination of a reducing acid, OA, and NaI is indispensable for effective reduction of GO in the current study and this unique combination (1) allows for tunable control over the volume of the thus-prepared graphene assemblies and (2) enables 3D graphene assemblies to be prepared from the GO suspension with a wide range of concentrations (0.1 to 4.5 mg mL-1). To the best of our knowledge, the GO concentration of 0.1 mg mL-1 is the lowest GO concentration ever reported for preparation of 3D graphene assemblies. The thus-prepared 3D graphene assemblies exhibit low density, highly porous structures, and electrically conducting properties. As a proof of concept, we show that by infiltrating a responsive polymer of polydimethylsiloxane (PDMS) into the as-resulted 3D conducting network of graphene, a conducting composite is obtained, which can be used as a sensing device for differentiating organic solvents with different polarity. © 2012 The Royal Society of Chemistry.

  8. Influence of TEM specimen preparation on chemical composition of Pb(Mg1/3Nb2/3)O3-PbTiO3 single crystals.

    Science.gov (United States)

    Srot, Vesna; Gec, Medeja; van Aken, Peter A; Jeon, Jae-Ho; Ceh, Miran

    2014-07-01

    The influences of different transmission electron microscopy (TEM) specimen preparation techniques on the chemical composition of Pb(Mg1/3Nb2/3)O3-PbTiO3 (PMN-PT) single crystals was studied. Ion-milled samples where no cooling with liquid nitrogen (L-N2) was applied show permanently changed composition also deep inside the bulk material. When the PMN-PT samples were cooled to L-N2 temperature during the ion-milling process and in addition lower accelerating voltages were used, the chemical composition was altered only in the thinnest parts close to the specimen edge. Samples prepared using only tripod polishing technique show compositional irregularities close to the specimen edge. For the preparation of lead-containing samples, such as PMN-PT single crystals, a combination of tripod polishing and short Ar-ion-milling at low accelerating voltages while cooling the samples to liquid nitrogen temperature proved to be the most suitable to obtain artefact-free electron-transparent TEM lamellae. PMID:24811990

  9. Preparation of activated carbon from acacia arabica by chemical activation for possible use in the treatment of chemical activation for possible use in the treatment of textile effluents

    International Nuclear Information System (INIS)

    Wood of Acacia Arabica syn. A. Nilotica, a locally available tree was used for the preparation of porous activated carbon for adsorption of dyes from aqueous solutions. The broken pieces of wood (6-10 mm size) were semicarbonized at 350 degree C in an atmosphere of N/sub 2/ gas and then impregnated with varying concentration of ZnCl/sub 2/ solution. The dried samples were sieved and carbonized under nitrogen atmosphere at various temperatures for activation. The porosity of the resulting carbon increased with the carbonization temperature to a maximum and then started decreasing with further increase in temperature. The optimum conditions for the production of activated carbon from kikar wood were observed to be carbonization temperature of 700 degree C for one hour with impregnation of wood to ZnCl/sub 2/ ratio of 1:2.5. The prepared activated carbon was evaluated with standard test methods and found to have high active surface area (Maximum Iodine No. 890). The possible industrial utility of the produced activated carbon was examined by adsorption of Congo red dye from its solutions. Different parameters including agitation time, adsorbent dose and temperature of adsorption were studied for finding the optimum conditions for maximum adsorption of the dye. Maximum removal of the dye (99%) was observed at 80 degree C with agitation time of 30min and activated carbon dose of 0.5g/100 ml solution for an initial concentrations of 100 mg/l of the dye. (author)

  10. Preparation of low molecular weight chitosan by a combination of chemical treatment and 60Co gamma radiation

    International Nuclear Information System (INIS)

    A low molecular weight chitosan finds potential applications in agriculture, medicine, personal health care, cosmetics etc. Chitosan undergoes depolymerization when exposed to ionizing radiation, therefore 60 Co gamma rays or electron beam irradiation appears to be the most promising way to prepare a low molecular weight chitosan

  11. Storage stability of margarines produced from enzymatically interesterified fats compared to those prepared by conventional methods - Chemical properties

    DEFF Research Database (Denmark)

    Zhang, Hong; Jacobsen, Charlotte; Pedersen, Lars Saaby;

    2006-01-01

    interesterification, including further treatment stages, might be responsible for the development of a high PV in the margarine produced from the chemically interesterified fat. However, the contents of volatiles did not show the same tendency as observed for PV for the margarines stored at 25øC during 12wk. Storage......In this study, four margarine hardstocks were produced, two from enzymatically interesterified fats at 80 and 100% conversion, one from chemically randomized fat and one from physically mixed fat. These four hardstocks, blended with 50% sunflower oil, were mainly used for the production of table...... margarines in a pilot plant. Storage stability studies were carried out at storage temperatures of 5 and 25øC for 12wk. Margarines from the enzymatically interesterified fats were compared to the margarines produced by the conventional methods (chemical interesterification and physical blending) and to...

  12. Synthesis and photocatalytic activity of TiO2 nanoparticles prepared by chemical vapor condensation method with different precursor concentration and residence time.

    Science.gov (United States)

    Chin, Sungmin; Park, Eunseuk; Kim, Minsu; Bae, Gwi-Nam; Jurng, Jongsoo

    2011-10-15

    Nanosized TiO(2) photocatalysts were synthesized using a chemical vapor condensation method under a range of synthesis conditions (precursor vapor concentration and residence time in a tubular electric furnace). X-ray diffraction showed that the prepared TiO(2) powders consisted mainly of anatase (>94%) with a small amount of rutile. The mean particle diameter from the Brunauer-Emmett-Teller surface area and transmission electron microscopy measurements ranged from 9.4 to 16.6 nm. The specific surface area (92.5-163.5 m(2) g(-1)) of the prepared TiO(2) powders was found to be dependent on the synthesis conditions. The content of hydroxyl groups on the surface of the prepared TiO(2) sample was higher than those on commercial TiO(2), resulting in increased photocatalytic oxidation. The photocatalytic activity of the TiO(2) samples prepared in a methylene blue solution was strongly dependent on the crystallinity and specific surface area, which were affected by the TTIP vapor concentration and residence time. PMID:21802692

  13. STORAGE OF CHEMICALLY PRETREATED WHEAT STRAW – A MEANS TO ENSURE QUALITY RAW MATERIAL FOR PULP PREPARATION

    Directory of Open Access Journals (Sweden)

    Terttu Heikkilä

    2010-07-01

    Full Text Available The aim of this study was to evaluate effects of chemical pretreatment and storage on non-wood pulping and on pulp quality. The processes studied were hot water treatment followed by alkaline peroxide bleaching or soda cooking. The results showed that it is possible to store wheat straw outside for at least one year without significant changes in the raw material chemical composition and without adverse effects on the resulting pulp quality. The results are significant to the industry using non-woods to ensure the availability and the quality of the raw-material throughout the year in spite of the short harvesting time.

  14. Effect of wet-chemical substrate smoothing on passivation of ultrathin-SiO2/n-Si(111) interfaces prepared with atomic oxygen at thermal impact energies

    Science.gov (United States)

    Angermann, Heike; Gref, Orman; Stegemann, Bert

    2011-12-01

    Ultrathin SiO2 layers for potential applications in nano-scale electronic and photovoltaic devises were prepared by exposure to thermalized atomic oxygen under UHV conditions. Wet-chemical substrate pretreatment, layer deposition and annealing processes were applied to improve the electronic Si/SiO2 interface properties. This favourable effect of optimized wet-chemical pre-treatment can be preserved during the subsequent oxidation. The corresponding atomic-scale analysis of the electronic interface states after substrate pre-treatment and the subsequent silicon oxide layer formation is performed by field-modulated surface photovoltage (SPV), atomic force microscopy (AFM) and spectroscopic ellipsometry in the ultraviolet and visible region (UV-VIS-SE).

  15. Rapid mixing chemical oxidative polymerization: an easy route to prepare PANI coated small-diameter CNTs/PANI nanofibres composite thin film

    Indian Academy of Sciences (India)

    G Venkata Ramana; Balaji Padya; Vadali V S S Srikanth; P K Jain

    2014-05-01

    Composite thin film containing polyaniline (PANI) coated small diameter carbon nanotubes (SDCNTs)/PANI nanofibres (NFs) has been prepared using an easy in situ rapid mixing chemical oxidative polymerization method. SDCNTs thin film was obtained using thermal chemical vapour deposition method in a separate experiment, whilst PANI NFs are formed in situ during the synthesis of composite. In the composite, PANI coated SDCNTs are uniformly distributed among PANI NFs. The presence of SDCNTs during the composite synthesis does not influence the nucleation and growth of PANI NFs. Raman analysis shows a good interaction between PANI and SDCNTs. Room temperature d.c. electrical sheet resistance of SDCNTs/PANI NFs composite thin film surface is three orders lesser than that of PANI NFs thin film (PANI NFs have the same morphology as in the composite) synthesized using the same method but without the presence of SDCNTs.

  16. Effect of Rare Earth Oxide Content on Nanograined Base Metal Electrode Multilayer Ceramic Capacitor Powder Prepared by Aqueous Chemical Coating Method

    Science.gov (United States)

    Zhang, Yichi; Wang, Xiaohui; Kim, Jinyong; Li, Longtu

    2013-02-01

    The aqueous chemical coating route is highly effective in preparing BaTiO3 nanoparticles uniformly coated with additives. Such nanoparticles can be used to produce nano-grained temperature stable BaTiO3 ceramics with core-shell structure, fulfilling the need of next-generation ultrathin layer base metal electrode (BME) multilayer ceramic capacitors (MLCCs). Rare earth oxides are an important class of additives owing to their ability to fulfill both donor and acceptor roles. In this paper, the effects of Y2O3 and Ho2O3 co-dopant content on dielectric and microstructural properties were investigated. By applying chemical coating, BaTiO3-based high performance temperature stabilized ceramics with the average grain size of about 130 nm, which met the requirement of next generation BME MLCCs, were obtained.

  17. [Analysis of exposure to pepper spray as a part of preparing hospital to help victims of mass chemical incidents].

    Science.gov (United States)

    Chwaluk, Paweł; Topczewska, Elzbieta; Barwina, Małgorzata

    2012-01-01

    We analyzed an incident of exposure to pepper spray 35 persons, including 29 children. Medical procedures were difficult because of the lack of reliable information about the nature of exposure, lack of hospital action plan for chemical accidents and established principles of cooperation with poison control center, as well as the need of extensive medical documentation for each patient. PMID:23243951

  18. Influence of precursor solution parameters on chemical properties of calcium phosphate coatings prepared using Electrostatic Spray Deposition (ESD).

    NARCIS (Netherlands)

    Leeuwenburgh, S.C.G.; Wolke, J.G.C.; Schoonman, J.; Jansen, J.A.

    2004-01-01

    A novel coating technique, referred to as Electrostatic Spray Deposition (ESD), was used to deposit calcium phosphate (CaP) coatings with a variety of chemical properties. The relationship between the composition of the precursor solutions and the crystal and molecular structure of the deposited coa

  19. Thick Fe2O3, Fe3O4 films prepared by the chemical solution deposition method

    Czech Academy of Sciences Publication Activity Database

    Buršík, Josef; Košovan, P.; Šubrt, Jan

    2006-01-01

    Roč. 39, č. 2 (2006), s. 85-94. ISSN 0928-0707 R&D Projects: GA ČR GA203/01/0408 Institutional research plan: CEZ:AV0Z40320502 Keywords : chemical solution deposition * thick films * alpha-Fe2O3 Subject RIV: CA - Inorganic Chemistry Impact factor: 1.009, year: 2006

  20. Chemical studies on the preparation of magnetic nanoparticles coated with glycine and its application for removal of heavy metals

    Directory of Open Access Journals (Sweden)

    Jawaher Alzaidi

    2016-06-01

    Full Text Available The aim of this study is the preparation of magnetic nanoparticles and coating with glycine to remove heavy metals such as Cu+2. The magnetic nanoparticles were prepared by co-precipitation method using using ferrous sulphate and potassium nitrate in presence of potassium hydroxide. Different instrumental analysis such as XRD, TEM, SEM and EDAX were used to study the magnetic nanoparticles which produced and comparing it after coated with glycine. The optimum conditions which reflect the high efficiency of removal are pH 10, concentration of the heavy metal 200 ppm, dosage 0.05 g and for 24 h duration time. Therefore we recommend using magnetic nanoparticles coated with glycine for removal of heavy metals.

  1. Effect of growth temperature on the structural of Nd-doped silica prepared by the chemical method

    Energy Technology Data Exchange (ETDEWEB)

    Aghamkar, P. [Materials Science Lab, Department of Applied Physics, Guru Jambheshwar University of Science and Technology, Hisar-125001 (India); Department of Physics, Chaudhary Devi Lal University, Sirsa-125055 (India); Duhan, S. [Materials Science Lab, Department of Applied Physics, Guru Jambheshwar University of Science and Technology, Hisar-125001 (India)], E-mail: surender6561@yahoo.co.in; Kishore, N. [Materials Science Lab, Department of Applied Physics, Guru Jambheshwar University of Science and Technology, Hisar-125001 (India); Lal, Bhajan [Department of Physics, Chaudhary Devi Lal University, Sirsa-125055 (India)

    2009-03-15

    Silica gel doped with Nd{sub 2}O{sub 3} was prepared by solgel method, using tetra-ethoxysilane and Nd (NO{sub 3}){sub 3} as precursor materials and HCl as a catalyst. The prepared samples were submitted to thermal treatments in the temperature range from 600 up to 1200 deg. C. Structural changes were investigated by XRD, FTIR spectroscopy and SEM. The effect of thermal annealing on Nd-containing silica has been discussed in detail. At 900 deg. C (4 h) various structures formed, while a further increase of the temperature and annealing time resulted in the formation of cubic neodymia and neodymium disilicate crystallites. At constant sintering temperature 1200 deg. C for 6 h the samples show distinct formation of Nd{sub 2}O{sub 3} nanocrystallites with average size {approx}16 nm.

  2. Effect of growth temperature on the structural of Nd-doped silica prepared by the chemical method

    International Nuclear Information System (INIS)

    Silica gel doped with Nd2O3 was prepared by solgel method, using tetra-ethoxysilane and Nd (NO3)3 as precursor materials and HCl as a catalyst. The prepared samples were submitted to thermal treatments in the temperature range from 600 up to 1200 deg. C. Structural changes were investigated by XRD, FTIR spectroscopy and SEM. The effect of thermal annealing on Nd-containing silica has been discussed in detail. At 900 deg. C (4 h) various structures formed, while a further increase of the temperature and annealing time resulted in the formation of cubic neodymia and neodymium disilicate crystallites. At constant sintering temperature 1200 deg. C for 6 h the samples show distinct formation of Nd2O3 nanocrystallites with average size ∼16 nm

  3. Non-radioactive hybridization probes prepared by the chemical labelling of DNA and RNA with a novel reagent, photobiotin.

    OpenAIRE

    Forster, A C; McInnes, J L; Skingle, D C; Symons, R H

    1985-01-01

    A photo-activatable analogue of biotin, N-(4-azido-2-nitrophenyl)-N'-(N-d-biotinyl-3-aminopropyl)-N'-methyl-1,3- propanediamine (photobiotin), has been synthesized and used for the rapid and reliable preparation of large amounts of stable, non-radioactive, biotin-labelled DNA and RNA hybridization probes. Upon brief irradiation with visible light, photobiotin formed stable linkages with single- and double-stranded nucleic acids yielding probes which were purified from excess reagent by 2-buta...

  4. Sensory and physico-chemical characteristics of desserts prepared with egg products processed by freeze and spray drying

    OpenAIRE

    Marcelo Nunes de Jesús; Ana Beatriz Zanqui; Patrícia Valderrama; Augusto Tanamati; Swami Arêa Maruyama; Nilson Evelázio de Souza; Makoto Matsushita

    2013-01-01

    In this work, three freeze-dried (FD) egg products (whole egg (WE), egg yolk (EY) and egg white (EW)) were obtained and the acceptability of confections prepared with each was evaluated. Sensory analyses for confections were performed by hedonic testing with fifty panelists in each evaluation. The studied confections were: Condensed Milk Pudding (P), Quindim (Q) and Meringue (M). The results obtained for confections made with FD egg products were compared with the achieved through other formu...

  5. Adsorption of Hexavalent Chromium from Aqueous Solution Using Chemically Activated Carbon Prepared from Locally Available Waste of Bamboo (Oxytenanthera abyssinica)

    OpenAIRE

    Dula, Tamirat; Siraj, Khalid; Kitte, Shimeles Addisu

    2014-01-01

    This study reports on the adsorption of Hexavalent Chromium from aqueous solutions using activated carbon prepared from bamboo (Oxytenanthera abyssinica) waste by KOH activation heating in an electrical furnace at 1073 K for 3 hrs. Batch adsorption experiments were also carried out as a function of pH, contact time, initial concentration of the adsorbate, adsorbent dosage, and temperature of the solution. Kinetic studies of the data showed that the adsorption follows the pseudo-second-order k...

  6. Preparation and characterization of SnO2 thin film by chemical bath deposition method for solar cell application

    International Nuclear Information System (INIS)

    Full text: Tin oxide thin films were synthesized by chemical bath deposition method on glass substrate .The as-deposited thin films were characterized for compositional, structural, surface morphological, optical and electrical properties. The X-ray diffraction patterns of the sample indicate that all samples are polycrystalline structure. AFM images show that the films consist of small uniform grains and are free of pinholes. (author)

  7. Enhanced photocatalytic activity of Ag–ZnO hybrid plasmonic nanostructures prepared by a facile wet chemical method

    OpenAIRE

    Sini Kuriakose; Vandana Choudhary; Biswarup Satpati; Satyabrata Mohapatra

    2014-01-01

    We report the synthesis of Ag–ZnO hybrid plasmonic nanostructures with enhanced photocatalytic activity by a facile wet-chemical method. The structural, optical, plasmonic and photocatalytic properties of the Ag–ZnO hybrid nanostructures were studied by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), photoluminescence (PL) and UV–visible absorption spectroscopy. The effects of citrate concentration and Ag nanoparticle loadi...

  8. Structural and XPS studies of PSi/TiO2 nanocomposites prepared by ALD and Ag-assisted chemical etching

    International Nuclear Information System (INIS)

    Highlights: • Porous silicon/TiO2 nanocomposites have been investigated. • Morphology and chemical composition of PSi/TiO2 nanocomposites were established. • Valence-band XPS maximums for PSi/TiO2 nanocomposites were found and analyzed. - Abstract: PSi/TiO2 nanocomposites fabricated by atomic layer deposition (ALD) and metal-assisted chemical etching (MACE) were investigated. The morphology and phase structure of PSi/TiO2 nanocomposites were studied by means of scanning electron microscopy (SEM), transmission electron microscopy (TEM) with an energy dispersive X-ray spectroscopy (EDX) and Raman spectroscopy. The mean size of TiO2 nanocrystals was determined by TEM and Raman spectroscopy. X-ray photoelectron spectroscopy (XPS) was used to analyze the chemical elemental composition by observing the behavior of the Ti 2p, O 1s and Si 2p lines. TEM, Raman spectroscopy and XPS binding energy analysis confirmed the formation of TiO2 anatase phase inside the PSi matrix. The XPS valence band analysis was performed in order to investigate the modification of PSi/TiO2 nanocomposites electronic structure. Surface defects states of Ti3+ at PSi/TiO2 nanocomposites were identified by analyzing of XPS valence band spectra

  9. Partial chemical characterization of antigenic preparations of chromoblastomycosis agents Caracterização química parcial de preparações antigênicas de agentes da cromoblastomicose

    OpenAIRE

    Tania Fraga BARROS; de Resende, Maria Aparecida

    1999-01-01

    Antigenic preparations (saline, methylic, metabolic and exoantigens) of four agents of chromoblastomycosis, Fonsecaea pedrosoi, Phialophora verrucosa, Cladophialophora (Cladosporium) carrionii and Rhinocladiella aquaspersa were obtained. Partial chemical characterization of these antigenic preparations was obtained by determination of the levels of total lipids, protein, and carbohydrates, and identification of the main sterols and carbohydrates. Methylic antigens presented the highest lipid ...

  10. Investigation of deposition characteristics and properties of high-rate deposited silicon nitride films prepared by atmospheric pressure plasma chemical vapor deposition

    International Nuclear Information System (INIS)

    Silicon nitride (SiN x) films have been prepared at extremely high deposition rates by the atmospheric pressure plasma chemical vapor deposition (AP-PCVD) technique on Si(001) wafers from gas mixtures containing He, H2, SiH4 and N2 or NH3. A 150 MHz very high frequency (VHF) power supply was used to generate high-density radicals in the atmospheric pressure plasma. Deposition rate, composition and morphology of the SiN x films prepared with various deposition parameters were studied by scanning electron microscopy and Auger electron spectroscopy. Fourier transformation infrared (FTIR) absorption spectroscopy was also used to characterize the structure and the chemical bonding configurations of the films. Furthermore, etching rate with buffered hydrofluoric acid (BHF) solution, refractive index and capacitance-voltage (C-V) characteristics were measured to evaluate the dielectric properties of the films. It was found that effective passivation of dangling bonds and elimination of excessive hydrogen atoms at the film-growing surface seemed to be the most important factor to form SiN x film with a dense Si-N network. The C-V curve of the optimized film showed good interface properties, although further improvement was necessary for use in the industrial metal-insulator-semiconductor (MIS) applications

  11. Preparation of activated carbons from olive-tree wood revisited. I. Chemical activation with H{sub 3}PO{sub 4}

    Energy Technology Data Exchange (ETDEWEB)

    Ould-Idriss, A.; Cuerda-Correa, E.M.; Fernandez-Gonzalez, C.; Alexandre-Franco, M.F.; Gomez-Serrano, V. [Extremadura Univ., Badajoz (Spain). Dept. of Organic and Inorganic Chemistry; Stitou, M. [Univ. Abdelmalek Esaadi, Tetouan (Morocco). Dept. de Chimie; Macias-Garcia, A. [Extremadura Univ., Badajoz (Spain). Dept. of Mechanical, Energetic and Materials Engineering

    2011-02-15

    In the conditioning tasks of olive-tree a large amount of a woody residue is generated. Such a residue has been traditionally used as a domestic fuel. In the last decades, however, this kind of use has lost importance and the preparation of activated carbons from olive-tree wood appears as an attractive alternative to valorize this by-product. In this study, the optimization of the chemical activation method with phosphoric acid for the production of activated carbon has been analyzed. The results obtained clearly show that samples prepared at 350 and 400 C exhibit a discrete porous development. On the contrary, when the carbonization temperature increases above 450 C the presence of a well-developed mesoporosity is observed. The mercury intrusion curves indicate that the samples exhibit a noticeably developed mesopore volume as well as a wide variety of mesopores ranging from 40 up to 1100 Aa of diameter. If the appropriate conditions are used, it is possible to prepare activated carbons showing tailored properties in terms of micro- or mesoporous texture and surface area. (author)

  12. Preparation and characterization of Pd/Al2O3 and Pd nanoparticles as standardized test material for chemical and biochemical studies of traffic related emissions.

    Science.gov (United States)

    Leopold, K; Maier, M; Schuster, M

    2008-05-01

    Palladium model particles similar to those emitted from catalytic car exhaust converters were prepared and characterized with the intention of providing a standardized material for investigations of the chemical behavior and bioavailability of traffic related Pd emissions. Two series of Pd particles were prepared and characterized in detail: Pd nanoparticles (2-4 nm) dispersed on aluminum oxide particles of a diameter range between 0.1 to 30 microm and "Pd-only" nanoparticles of 5-10 nm in diameter. The Pd/alpha-Al2O3 particles are very similar to particles emitted from catalytic converters by mechanical abrasion. The Pd-only particles are useful e.g. for exposure studies in which the presence of aluminum could lead to interferences when studying biological and biochemical effects. The sample preparation procedure of both series was optimized in order to achieve elemental particles with proper sizes and a narrow size distribution. The obtained particles were characterized by transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM), selective area diffraction (SAD), laser granulometry and graphite furnace atomic absorption spectrometry (GFAAS) for the measurement of Pd concentrations. PMID:18279916

  13. PREPARATION OF CHEMICAL AND PHYSICAL CONJUGATES OF SELF-ASSEMBLING NANOPARTICLES WITH CELL-PENETRATING PEPTIDE AND DOXORUBICIN

    Directory of Open Access Journals (Sweden)

    Zhadyra Sagykyzy Shagyrova

    2015-09-01

    Full Text Available Abstract: Nano-sized carriers can help to reduce toxicity and improve clinical efficacy of drugs. Virus-like particles (VLPs are biocompatible and biodegradable self-assembling nanoparticles, which show great promise as carriers for substances for targeted delivery and controlled release. Either chemical conjugation of physical incorporation without formation of covalent bonds is possible to load substances of interest into VLPs.Objectives: To produce VLPs from recombinant viral capsid protein (HBcAg and test feasibility of methods of formation of chemical and physical conjugates of VLPs with substances of pharmacological interest.Methods: Virus-like particles composed from recombinant hepatitis B core antigen (HBcAg were produced by recombinant expression in E.coli and purified by successive centrifugation through sucrose gradients. Peptide transportan 10 was synthesized and used for carbodiimide (EDC-mediated conjugation to VLPs. Doxorubicin (DOX was loaded into the nucleic acid-containing VLPs to form physical conjugate.Results: VLPs with chemically attached moieties of cell-penetrating peptide transportan 10 were produced. The conjugate was examined in SDS-PAGE to confirm presence of conjugation products. Conjugation efficiency (molar ration peptide/protein in the conjugate reaches 0.5:1 (i.e. 50% of protein chains have one attached peptide moiety. The nucleic acid-containing VLPs can be loaded with the DOX forming stable non-covalent physical conjugate.Conclusion: Recombinantly expressed VLPs allow easy attaching of small molecules making them a convenient platform to develop drug carriers.

  14. Studies on the preparation of active oxygen-deficient copper ferrite and its application for hydrogen production through thermal chemical water splitting

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Hydrogen generation through thermal chemical water splitting technology has recently received in- creasingly international interest in the nuclear hydrogen production field. Besides the main known sulfur-iodine (S-I) cycle developed by the General Atomics Company and the UT3 cycle (iron, calcium, and bromine) developed at the University of Tokyo, the thermal cycle based on metal oxide two-step water splitting methods is also receiving research and development attention worldwide. In this work, copper ferrite was prepared by the co-precipitation method and oxygen-deficient copper ferrite was synthesized through first and second calcination steps for the application of hydrogen production by a two-step water splitting process. The crystal structure, properties, chemical composition and δ were investigated in detail by utilizing X-ray diffraction (XRD), thermogravimetry (TG) and differential thermal analysis (DTA), atomic absorption spectrometer (AAS), ultraviolet spectrophotometry (UV), gas chro- matography (GC), and so on. The experimental two-step thermal chemical cycle reactor for hydrogen generation was designed and developed in this lab. The hydrogen generation process of water splitting through CuFe2O4-δ and the cycle performance of copper ferrite regeneration were firstly studied and discussed.

  15. Studies on the preparation of active oxygen-deficient copper ferrite and its application for hydrogen production through thermal chemical water splitting

    Institute of Scientific and Technical Information of China (English)

    YU Bo; ZHANG Ping; ZHANG Lei; CHEN Jing; XU JingMing

    2008-01-01

    Hydrogen generation through thermal chemical water splitting technology has recently received in-creasingly international interest in the nuclear hydrogen production field. Besides the main known sulfur-iodine (S-I) cycle developed by the General Atomics Company and the UT3 cycle (iron, calcium, and bromine) developed at the University of Tokyo, the thermal cycle based on metal oxide two-step water splitting methods is also receiving research and development attention worldwide. In this work, copper ferrite was prepared by the co-precipitation method and oxygen-deficient copper ferrite was synthesized through first and second calcination steps for the application of hydrogen production by a two-step water splitting process. The crystal structure, properties, chemical composition and δwere investigated in detail by utilizing X-ray diffraction (XRD), thermogravimetry (TG) and differential thermal analysis (DTA), atomic absorption spectrometer (AAS), ultraviolet spectrophotometry (UV), gas chro-matography (GC), and so on. The experimental two-step thermal chemical cycle reactor for hydrogen generation was designed and developed in this lab. The hydrogen generation process of water splitting through CuFe2O4-δ and the cycle performance of copper ferrite regeneration were firstly studied and discussed.

  16. Preparation, Biodegradation of Coconut Oil Driven Chemically Modified Bovine Serum Albumin Microparticles of Encapsulated Cicer arietinum Amylase and Study of Their Application in Washing Detergents

    Directory of Open Access Journals (Sweden)

    Kirti Rani

    2014-10-01

    Full Text Available In present work, Cicer arietinum amylase was encapsulated by emulsification through covalent coupling by glutaraldehyde into chemically modified bovine serum albumin. Biodegradation of coconut oil driven emulsified bovine serum albumin encapsulated Cicer arietinum amylase was carried out by the alkaline protease for its controlled and sustained release of encapsulated enzyme from prepared microparticles of encapsulated Cicer arietinum amylase and its stability increased up to 6 months as compared to free enzyme. Its biodegradation was carried out by the using different concentration of alkaline protease (5U, 10U, 15U, 20U, 25U, 30U, 35U, 40U. Further, this coconut oil driven chemically modified bovine serum albumin microparticles of encapsulated Cicer arietinum amylase with alkaline protease were used with detergents for washing of stained cloths which have rust, gel pen ink, grease and chocolate strains. These chosen strains are very commonly present on uniforms of school going children which are very tough upon drying, hence, not to be easily vanish with well known brand detergents upon in one wash. But, the mixture solution of coconut oil driven chemically modified bovine serum albumin microparticles of encapsulated Cicer arietinum amylase along with alkaline protease were used with detergents powder for washing of these dry tough strains (rust, gel pen ink, grease and chocolate strains leads to vanishing these strains very fast with absolute clear results were found as compared to results of washing of stained cloths with detergents only.

  17. Preparation of conversion coating on Ti-6Al-4V alloy in mixed solution of phytic acid and ammonium fluoride through chemical modification

    Science.gov (United States)

    Li, Lanlan; He, Jian; Yang, Xu

    2016-05-01

    Conversion coatings on Ti-6Al-4V alloy was prepared through chemical modification in phytic acid and ammonium fluoride mixed solution. The influences of pH, time and the composition of solution on the microstructure of alloy surface were investigated. Scanning electron microscopy was used to observe the microstructure. The chemical composition of alloy surface before and after modification was investigated by energy dispersive X-ray spectroscopy. The results indicated that a conversion coating could be formed on the Ti-6Al-4V alloy in a mixed solution of phytic acid and ammonium fluoride, the growth and microstructure of the conversion coatings were critically dependent on the pH, time and concentration of phytic acid and ammonium fluoride. In 100 mg/ml phytic acid containing 125 mg/ml ammonium fluoride solution with a pH of 6, a compact conversion coating with the thickness of about 4.7 μm formed after 30 min immersion on Ti-6Al-4V alloy surface. The preliminary evaluation of bioactivity of conversion coating was performed by in vitro cell experiments. The results showed that this chemical modification method is a promising surface modification technique for Ti-6Al-4V alloy inplants.

  18. Effect of applied dc bias voltage on composition, chemical bonding and mechanical properties of carbon nitride films prepared by PECVD

    Institute of Scientific and Technical Information of China (English)

    LI Hong-xuan; XU Tao; HAO Jun-ying; CHEN Jian-min; ZHOU Hui-di; XUE Qun-ji; LIU Hui-wen

    2004-01-01

    Carbon nitride films were deposited on Si (100) substrates using plasma-enhanced chemical vapor deposition (PECVD) technique from CH4 and N2 at different applied dc bias voltage. The microstructure, composition and chemical bonding of the resulting films were characterized by Raman spectroscopy, Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). The mechanical properties such as hardness and elastic modulus of the films were evaluated using nano-indentation. As the results, the Raman spectra, showing the G and D bands, indicate the amorphous structure of the films. XPS and FTIR measurements demonstrate the existence of various carbon-nitride bonds in the films and the hydrogenation of carbon nitride phase. The composition ratio of N to C, the nano-hardness and the elastic modulus of the carbon nitride films increase with increasing dc bias voltage and reach the maximums at a dc bias voltage of 300 V, then they decrease with further increase of the dc bias voltage. Moreover, the XRD analyses indicate that the carbon nitride film contains some polycrystalline C3N4 phase embedded in the amorphous matrix at optimized deposition condition of dc bias voltage of 300 V.

  19. Microstructure and properties of tungsten–samarium oxide composite prepared by a novel wet chemical method and spark plasma sintering

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • W–Sm2O3 powders were synthesized by a novel wet chemical method. • Oxide particles were distributed in both the tungsten grains and grain boundaries. • Tensile strength of W–Sm2O3 samples was higher than those of pure W samples. - Abstract: W–1 wt% Sm2O3 powders doped with highly uniform Sm2O3 were successfully synthesized by a novel wet chemical method followed by hydrogen reduction. The powders were consolidated by spark plasma sintering (SPS) at 1800 °C to suppress grain growth during sintering. The FE-SEM and HRTEM analysis, tensile test and thermal conductivity measurements were used to characterize these samples. The grain size, relative density of the bulk samples fabricated by SPS sintering were 4 μm and 97.8%, respectively. The tensile strength values of Sm2O3/W samples were higher than those of pure W samples. As the temperature rises from 25 to 800 °C, the thermal conductivity of pure W and W–1 wt% Sm2O3 composites decreased with the same trend and the thermal conductivity of both samples was above 160 W/m K at room temperature

  20. Effect of gamma irradiation on microbial load, chemical and sensory properties of chicken kabab and sausage; as prepared chilled meals

    International Nuclear Information System (INIS)

    Chicken kabab and sausage were treated with 0, 2, 4 or 6 kGy doses of gamma irradiation in a 60CO package irradiator. Treated and untreated samples were kept in a refrigerator (1-4 degree centigrade). Microbiological, chemical and sensory characteristics of chicken kabab and sausage were evaluated at 0, 1, 2, 3, 4, and 5 months of storage. Proximate composition and sensory evaluation of the chicken kabab and sausage were also investigated, but only immediately after treatment. Irradiation did not influence the major constituents of chicken kabab and sausage (moisture, protein and fats). Gamma irradiation decreased the microbial load and increased the shelf-life of chicken kabab and sausage. The dose needed to decrease by 1 log cfu/g (D10 value) of Salmonella spp and E coli. numbers were 213 and 400 Gy in chicken kabab, while 345 and 250 Gy in chicken sausage, respectively. The chemical parameters, total acidity, volatile basic nitrogen (VBN), and thiobarbituric acid reactive substances (TBARS), which were chosen as the indices of freshness, were all well within the acceptable limit for up to 5 months for chicken kabab and sausage treated with 4 and 6 kGy. Sensory evaluation showed no significant differences between irradiated and non-irradiated samples. (author)

  1. Role of carbon in titania as visible-light photocatalyst prepared by flat-flame chemical vapor condensation method

    International Nuclear Information System (INIS)

    In this article, the authors report that titania nanopowders synthesized by low-pressure flat-flame metal-organic chemical vapor condensation show visible-light photocatalytic ability. Using acetylene and oxygen as fuel and oxidizer for the flame, the titanium isopropoxide was decomposed and oxidized, and the nanoparticles of titania were formed. From the methylene blue decomposition study they found that the powder synthesized under low precursor feed rate possesses high photocatalytic efficiency under illumination of visible light. The visible-light absorption is resort to the presence of carbon since no other chemical elements were found associated with titania. The presence of carbon species is coincident with the presence of visible-light absorption and carbon is in the form of C-C bond. It also suggests that carbon species are associated with catalytic site on anatase surface so that carriers generated by photon absorption by the carbon species can transfer quickly onto catalytic sites and perform the subsequent catalytic reactions. A possibly unreported mechanism of visible-light TiO2 photocatalysis induced by carbon doping is identified.

  2. XRD and XPS characterization of mixed valence Mn3O4 hausmannite thin films prepared by chemical spray pyrolysis technique

    International Nuclear Information System (INIS)

    Spray pyrolysis technique has been employed successfully for the synthesis of single phase mixed valence spinel hausmannite (Mn3O4) thin films using alcoholic start solution of manganese acetate (Mn(CH3COO)2.4H2O) on pyrex glass substrates at atmospheric pressure using air as a carrier gas. Thermal decomposition of the precursor in the temperature range 320-490 deg. C led to the formation of Mn3O4 phase as revealed from the thermogravimetry analysis. Prepared samples are characterized by X-ray diffraction that shows spinel structure with space group I41/amd. Pure and well crystallized specimen is subjected to X-ray photoelectron spectroscopy for the surface chemistry investigation of these systems at a molecular level. Surface Mn/O ratio is compared to the bulk composition of the sample. Atomic force micrographs revealed that the morphology and the surface grains of the films largely influenced by the substrate temperature.

  3. Optical properties of TiO{sub 2} thin films prepared by chemical spray pyrolysis from aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Ayouchi, R.; Casteleiro, C.; Schwarz, R. [Departamento de Fisica, Instituto Superior Tecnico, Av. Rovisco Pais 1, 1049-001 Lisboa (Portugal); Barrado, J.R.; Martin, F. [Laboratorio de Materiales y Superficie (Unidad Asociada al CSIC), Departamento de Fisica Aplicada I e Departamento de Ingenieria Quimica, Universidad de Malaga, 29071 Malaga (Spain)

    2010-04-15

    Titanium dioxide (TiO{sub 2}) is known to have three different kinds of polymorphous crystalline forms: rutile, anatase, and brookite. The rutile phase is always formed at higher temperatures, while the anatase phase is formed at lower temperatures and transformed into rutile phase above 800 C. Various deposition techniques have been developed for depositing TiO{sub 2} thin films, including evaporation, sputtering, chemical vapour deposition and thermal oxidation of titanium. Among them, the Chemical Spray Pyrolysis (CSP) technique has many advantages, such as good conformal coverage, the possibility of epitaxial growth and the application to large area deposition. Also, this method is low cost and it is easy to control the deposition growth parameters. In the present work, TiO{sub 2} thin films have been deposited on p-Si(001) and fused silica substrates by Chemical Spray Pyrolysis (CSP) method from aqueous solution containing titanium (IV) isopropoxide (Ti[OCH(CH{sub 3}){sub 2}]{sub 4}). As-deposited thin films show anatase polycrystalline structure, and rutile phase formed for films annealed at 750 C. SEM images have confirmed a smooth and crack-free surface with low surface roughness. X-ray photoelectron spectroscopy (XPS) combined with 4 keV Ar{sup +} depth profiling has shown that crystallized films correspond to TiO{sub 2}. Residual carbon coming from the organic precursor solution is only detected at the surface of the film. Thin films deposited on fused silica were highly transparent (more than 85%), with an indirect optical band gap of 3,43 and 3,33 eV for as-deposited and annealed films, respectively, and refractive indexes in the range between 2.01-2.29. Spectroscopic Ellipsometry (SE) also has been used to extract optical parameters. SE data fitted to triple-layer physical model revealed the same tendency to increase refractive index in annealed films. (copyright 2010 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  4. Microwave dielectric properties of BiFeO3 thin film prepared by aqueous chemical solution deposition method

    Directory of Open Access Journals (Sweden)

    Ričardas Sobiestianskas

    2009-12-01

    Full Text Available We report high frequency dielectric properties of multiferroic BiFeO3 (BFO thin film deposited by means of aqueous chemical solution deposition on platinized silicon substrate. The structure analysis of the BFO performed by X-ray diffraction and energy dispersive analysis showed pure, single-phase quality of the thin films. The impedance measurements were performed by vector network analyzer in frequency range 100 MHz to 10 GHz at ambient temperature. The film leakage currents dominate dielectric losses at low frequencies. The dielectric constant of the film is around 40. An internal charged defects acting as energy traps for electrons dominate dielectric losses in the frequency region above 4 GHz.

  5. Chemical fingerprinting and quantitative analysis of a Panax notoginseng preparation using HPLC-UV and HPLC-MS

    Directory of Open Access Journals (Sweden)

    Shao Qing

    2011-02-01

    Full Text Available Abstract Background Xuesaitong (XST injection, consisting of total saponins from Panax notoginseng, was widely used for the treatment of cardio- and cerebro-vascular diseases in China. This study develops a simple and global quality evaluation method for the quality control of XST. Methods High performance liquid chromatography-ultraviolet detection (HPLC-UV was used to identify and quantify the chromatographic fingerprints of the XST injection. Characteristic common peaks were identified using HPLC with photo diode array detection/electrospray ionization tandem mass spectrometry (HPLC-PDA/ESI-MSn. Results Representative fingerprints from ten batches of samples showed 27 'common saponins' all of which were identified and quantified using ten reference saponins. Conclusion Chemical fingerprinting and quantitative analysis identified most of the common saponins for the quality control of P. notoginseng products such as the XST injection.

  6. Characterization of thin TiO2 films prepared by plasma enhanced chemical vapour deposition for optical and photocatalytic applications

    International Nuclear Information System (INIS)

    Thin titanium oxide films were deposited using a radio frequency (RF) plasma enhanced chemical vapour deposition method. Their optical properties and thickness were determined by means of ultraviolet-visible absorption spectrophotometry. Films of the optical parameters very close to those of titanium dioxide have been obtained at the high RF power input. Their optical quality is high enough to allow for their use in a construction of stack interference optical filters. At the same time, these materials exhibit strong photocatalytic effects. The results of structural analysis, carried out by Raman Shift Spectroscopy, show that the coatings posses amorphous structure. However, Raman spectra of the same films subjected to thermal annealing at 450 oC disclose an appearance of a crystalline form, namely that of anatase. Surface morphology of the films has also been characterized by Atomic Force Microscopy revealing granular, broccoli-like topography of the films.

  7. Structural, optical and photocatalytic properties of flower-like ZnO nanostructures prepared by a facile wet chemical method

    Directory of Open Access Journals (Sweden)

    Sini Kuriakose

    2013-11-01

    Full Text Available Flower-like ZnO nanostructures were synthesized by a facile wet chemical method. Structural, optical and photocatalytic properties of these nanostructures have been studied by X-ray diffraction (XRD, scanning electron microscopy (SEM, transmission electron microscopy (TEM, photoluminescence (PL and UV–vis absorption spectroscopy. SEM and TEM studies revealed flower-like structures consisting of nanosheets, formed due to oriented attachment of ZnO nanoparticles. Flower-like ZnO structures showed enhanced photocatalytic activity towards sun-light driven photodegradation of methylene blue dye (MB as compared to ZnO nanoparticles. XRD, UV–vis absorption, PL, FTIR and TEM studies revealed the formation of Zn(OH2 surface layer on ZnO nanostructures upon ageing. We demonstrate that the formation of a passivating Zn(OH2 surface layer on the ZnO nanostructures upon ageing deteriorates their efficiency to photocatalytically degrade of MB.

  8. Monolithically integrated InGaAs/InP MSM-FET photoreceiver prepared by chemical beam epitaxy

    International Nuclear Information System (INIS)

    The authors demonstrate the first monolithic integration of a metal-semiconductor-metal (MSM) InGaAs photodetector with an FET and resistors into a high-impedance front-end photoreceiver circuit. The sample was grown in a single step by chemical beam epitaxy, and standard processing steps for making FET's were used to fabricate the receiver circuit. Semi-insulating Fe-doped InP layers were used as the insulating gate of the FET, the barrier enhancement layer in the MSM photodetector, and the electrical isolation layer between the photodetector and the electronic circuit. A bit error rate of less than 10-9 at 200 Mbits/s has been achieved with this preliminary circuit for an optical power of - 17 dBm

  9. Characterization of the ZnO thin film prepared by single source chemical vapor deposition under low vacuum condition

    Institute of Scientific and Technical Information of China (English)

    DENG; Hong(邓宏); B.; GONG; A.; J.; Petrella; J.; J.; Russell; R.; N.; Lamb

    2003-01-01

    A novel technique is developed for growing high quality ZnO thin films by means of single source chemical vapor deposition (SS CVD) under low vacuum conditions with the precursor of zinc carbamate Zn4O(CO2Net2)6. SEM, AFM and XRD studies show that the resultant thin films have high density, smooth surface, uniform polycrystalline structure and excellent c-axis orientation. XPS investigation indicates that the ZnO films are free of decomposed precursor residues in the bulk. Careful quantitative XPS analysis reveals that the ZnO films are stoichiometric with O/Zn atomic ratio very close to that of ZnO single crystal.

  10. Preparation of ZnO nanorods and special lath-like crystals by aqueous chemical growth (ACG) method

    International Nuclear Information System (INIS)

    Special lath-like ZnO crystals and arrays of well-aligned ZnO nano/micro-composite rods were synthesized on ZnO seed-coated glass substrates by aqueous chemical growth (ACG) method. PEG was added into the seed precursor solution to obtain seed layers with different textures, on which nano/micro-composite rods were formed. Special lath-like crystals were fabricated by prolonging the growth time to 48 h. X-ray diffraction and scanning electron microscopy analyses reveal that highly c-oriented rod crystals grow vertically from the substrate. The possible growth mechanism concerning special lath-like crystals and nano/micro-composite rods has been discussed

  11. Raman Spectroscopic Study of Carbon Nanotubes Prepared Using Fe/ZnO-Palm Olein-Chemical Vapour Deposition

    Directory of Open Access Journals (Sweden)

    Syazwan Afif Mohd Zobir

    2012-01-01

    Full Text Available Multiwalled carbon nanotubes (MWCNTs were synthesized using Fe/ZnO catalyst by a dual-furnace thermal chemical vapor deposition (CVD method at 800–1000°C using nitrogen gas with a constant flow rate of 150 sccm/min as a gas carrier. Palm olein (PO, ferrocene in the presence of 0.05 M zinc nitrate, and a p-type silicon wafer were used as carbon source, catalyst precursor, and sample target, respectively. D, G, and G′ bands were observed at 1336–1364, 1559–1680, and 2667–2682 cm-1, respectively. Carbon nanotubes (CNTs with the highest degree of crystallinity were obtained at around 8000°C, and the smallest diameter of about 2 nm was deposited on the silicon substrate at 1000°C.

  12. Nanoscale multilayered and porous carbide interphases prepared by pressure-pulsed reactive chemical vapor deposition for ceramic matrix composites

    Energy Technology Data Exchange (ETDEWEB)

    Jacques, S., E-mail: jacques@lcts.u-bordeaux1.fr [LCTS, University of Bordeaux 1, CNRS, Herakles-Safran, CEA, 3 allee de la Boetie, F-33600 Pessac (France); Jouanny, I.; Ledain, O.; Maillé, L.; Weisbecker, P. [LCTS, University of Bordeaux 1, CNRS, Herakles-Safran, CEA, 3 allee de la Boetie, F-33600 Pessac (France)

    2013-06-15

    In Ceramic Matrix Composites (CMCs) reinforced by continuous fibers, a good toughness is achieved by adding a thin film called “interphase” between the fiber and the brittle matrix, which acts as a mechanical fuse by deflecting the matrix cracks. Pyrocarbon (PyC), with or without carbide sub-layers, is typically the material of choice to fulfill this role. The aim of this work was to study PyC-free nanoscale multilayered carbide coatings as interphases for CMCs. Nanoscale multilayered (SiC–TiC){sub n} interphases were deposited by pressure-Pulsed Chemical Vapor Deposition (P-CVD) on single filament Hi-Nicalon fibers and embedded in a SiC matrix sheath. The thicknesses of the carbide interphase sub-layers could be made as low as a few nanometers as evidenced by scanning and transmission electron microscopy. By using the P-ReactiveCVD method (P-RCVD), in which the TiC growth involves consumption of SiC, it was not only possible to obtain multilayered (SiC–TiC){sub n} films but also TiC films with a porous multilayered microstructure as a result of the Kirkendall effect. The porosity in the TiC sequences was found to be enhanced when some PyC was added to SiC prior to total RCVD consumption. Because the porosity volume fraction was still not high enough, the role of mechanical fuse of the interphases could not be evidenced from the tensile curves, which remained fully linear even when chemical attack of the fiber surface was avoided.

  13. Nanoscale multilayered and porous carbide interphases prepared by pressure-pulsed reactive chemical vapor deposition for ceramic matrix composites

    International Nuclear Information System (INIS)

    In Ceramic Matrix Composites (CMCs) reinforced by continuous fibers, a good toughness is achieved by adding a thin film called “interphase” between the fiber and the brittle matrix, which acts as a mechanical fuse by deflecting the matrix cracks. Pyrocarbon (PyC), with or without carbide sub-layers, is typically the material of choice to fulfill this role. The aim of this work was to study PyC-free nanoscale multilayered carbide coatings as interphases for CMCs. Nanoscale multilayered (SiC–TiC)n interphases were deposited by pressure-Pulsed Chemical Vapor Deposition (P-CVD) on single filament Hi-Nicalon fibers and embedded in a SiC matrix sheath. The thicknesses of the carbide interphase sub-layers could be made as low as a few nanometers as evidenced by scanning and transmission electron microscopy. By using the P-ReactiveCVD method (P-RCVD), in which the TiC growth involves consumption of SiC, it was not only possible to obtain multilayered (SiC–TiC)n films but also TiC films with a porous multilayered microstructure as a result of the Kirkendall effect. The porosity in the TiC sequences was found to be enhanced when some PyC was added to SiC prior to total RCVD consumption. Because the porosity volume fraction was still not high enough, the role of mechanical fuse of the interphases could not be evidenced from the tensile curves, which remained fully linear even when chemical attack of the fiber surface was avoided.

  14. Nanoscale multilayered and porous carbide interphases prepared by pressure-pulsed reactive chemical vapor deposition for ceramic matrix composites

    Science.gov (United States)

    Jacques, S.; Jouanny, I.; Ledain, O.; Maillé, L.; Weisbecker, P.

    2013-06-01

    In Ceramic Matrix Composites (CMCs) reinforced by continuous fibers, a good toughness is achieved by adding a thin film called "interphase" between the fiber and the brittle matrix, which acts as a mechanical fuse by deflecting the matrix cracks. Pyrocarbon (PyC), with or without carbide sub-layers, is typically the material of choice to fulfill this role. The aim of this work was to study PyC-free nanoscale multilayered carbide coatings as interphases for CMCs. Nanoscale multilayered (SiC-TiC)n interphases were deposited by pressure-Pulsed Chemical Vapor Deposition (P-CVD) on single filament Hi-Nicalon fibers and embedded in a SiC matrix sheath. The thicknesses of the carbide interphase sub-layers could be made as low as a few nanometers as evidenced by scanning and transmission electron microscopy. By using the P-ReactiveCVD method (P-RCVD), in which the TiC growth involves consumption of SiC, it was not only possible to obtain multilayered (SiC-TiC)n films but also TiC films with a porous multilayered microstructure as a result of the Kirkendall effect. The porosity in the TiC sequences was found to be enhanced when some PyC was added to SiC prior to total RCVD consumption. Because the porosity volume fraction was still not high enough, the role of mechanical fuse of the interphases could not be evidenced from the tensile curves, which remained fully linear even when chemical attack of the fiber surface was avoided.

  15. Characterisation of samarium and nitrogen co-doped TiO2 films prepared by chemical spray pyrolysis

    International Nuclear Information System (INIS)

    Highlights: ► The TiO2:N:Sm thin films deposited by chemical spray pyrolysis have anatase structure. ► According to XPS, N is incorporated into the TiO2 matrix. ► N-doping increases and Sm-doping reduces the crystallite size of the TiO2:N:Sm films. ► Incorporation of N strongly suppresses the Sm3+ PL emission. - Abstract: The sol–gel chemical spray pyrolysis method was used to deposit samarium and nitrogen co-doped TiO2 films onto a quartz substrate at a growth temperature of 450 °C using pulsed spray solution feed, followed by annealing at 500 °C for 2 h in air. The obtained films exhibited anatase structure independent of the doping level. According to XRD analysis, the mean crystallite size of the undoped TiO2, TiO2:N(25) and TiO2:N(5):Sm(5) films was 32, 38 and 20 nm, respectively. According to AFM, the undoped TiO2 film consisted of agglomerates with a size of 30–200 nm. N-doping (25 at%) transformed the agglomerates into individually distinctive grains with a size of ca. 30 nm, while Sm doping (5 at%) caused a significant decrease in the average diameter of the agglomerates to ca. 100 nm. The RMS roughness of the undoped TiO2 film was 1.7 nm; doping resulted in the formation of smoother films with RMS roughness of 0.9–1.4 nm. XPS data indicated that the Sm and N dopants were incorporated into the TiO2 crystal lattice and/or adsorbed on the surface of the film. An increasing nitrogen concentration in the spray solution correlates to a systematic suppressing of the photoluminescence intensity of Sm3+.

  16. Effect of chemical fixatives on accurate preservation of Escherichia coli and Bacillus subtilis structure in cells prepared by freeze-substitution

    International Nuclear Information System (INIS)

    Five chemical fixatives were evaluated for their ability to accurately preserve bacterial ultrastructure during freeze-substitution of select Escherichia coli and Bacillus subtilis strains. Radioisotopes were specifically incorporated into the peptidoglycan, lipopolysaccharide, and nucleic acids of E. coli SFK11 and W7 and into the peptidoglycan and RNA of B. subtilis 168 and W23. The ease of extraction of radiolabels, as assessed by liquid scintillation counting during all stages of processing for freeze-substitution, was used as an indicator of cell structural integrity and retention of cellular chemical composition. Subsequent visual examination by electron microscopy was used to confirm ultrastructural conformation. The fixatives used were: 2% (wt/vol) osmium tetroxide and 2% (wt/vol) uranyl acetate; 2% (vol/vol) glutaraldehyde and 2% (wt/vol) uranyl acetate; 2% (vol/vol) acrolein and 2% (wt/vol) uranyl acetate; 2% (wt/vol) gallic acid; and 2% (wt/vol) uranyl acetate. All fixatives were prepared in a substitution solvent of anhydrous acetone. Extraction of cellular constituents depended on the chemical fixative used. A combination of 2% osmium tetroxide-2% uranyl acetate or 2% gallic acid alone resulted in optimum fixation as ascertained by least extraction of radiolabels. In both gram-positive and gram-negative organisms, high levels of radiolabel were detected in the processing fluids in which 2% acrolein-2% uranyl acetate, 2% glutaraldehyde-2% uranyl acetate, or 2% uranyl acetate alone were used as fixatives. Ultrastructural variations were observed in cells freeze-substituted in the presence of different chemical fixatives. We recommend the use of osmium tetroxide and uranyl acetate in acetone for routine freeze-substitution of eubacteria, while gallic acid is recommended for use when microanalytical processing necessitates the omission of osmium

  17. Preparation and use of chemically modified MCM-41 and silica gel as selective adsorbents for Hg(II) ions

    International Nuclear Information System (INIS)

    Adsorbents for Hg(II) ion extraction were prepared using amorphous silica gel and ordered MCM-41. Grafting with 2-(3-(2-aminoethylthio)propylthio)ethanamine was used to functionalize the silica. The functionalized adsorbents were characterized by nitrogen adsorption, X-ray diffraction, 13C MAS NMR spectroscopy and thermogravimetric analysis. The adsorption properties of the modified silica gel and MCM-41 were compared using batch method. The effect of pH, stirring time, ionic strength and foreign ions were studied. The extraction of Hg(II) ions occurred rapidly with the modified MCM-41 and the optimal pH range for the extraction by the modified materials was pH 4-7. Foreign ions, especially Cl- had some effect on the extraction efficiency of the modified silica gel and the modified MCM-41. The adsorption behavior of both adsorbents could be described by a Langmuir model at 298 K, and the maximum adsorption capacity of the modified silica gel and MCM-41 at pH 3 was 0.79 and 0.70 mmol g-1, respectively. The modified MCM-41 showed a larger Langmuir constant than that of the modified silica gel, indicating a better ability for Hg(II) ion adsorption. The results indicate that the structure of the materials affects the adsorption behavior. These materials show a potential for the application as effective and selective adsorbents for Hg(II) removal from water

  18. Sensory and physico-chemical characteristics of desserts prepared with egg products processed by freeze and spray drying

    Directory of Open Access Journals (Sweden)

    Marcelo Nunes de Jesús

    2013-09-01

    Full Text Available In this work, three freeze-dried (FD egg products (whole egg (WE, egg yolk (EY and egg white (EW were obtained and the acceptability of confections prepared with each was evaluated. Sensory analyses for confections were performed by hedonic testing with fifty panelists in each evaluation. The studied confections were: Condensed Milk Pudding (P, Quindim (Q and Meringue (M. The results obtained for confections made with FD egg products were compared with the achieved through other formulations of the same desserts made with fresh (F or spray-dried (SD egg products. The sensory analysis results for confections made with FD egg products showed good acceptance by panelists. A principal component analysis of the sensory evaluation data was carried out to identify similarities between the different egg products. The PCA supported the conclusion that FD egg products can substitute their fresh and SD counterparts in dessert formulations with good acceptability while keeping the advantages conferred by the freeze-drying method.

  19. Preparation of carbonaceous adsorbents from sewage sludge by chemical activation process - application to air and water treatments

    Energy Technology Data Exchange (ETDEWEB)

    Rio, S.; Le Coq, L.; Faur-Brasquet, C.; Le Cloirec, P. [Ecole des Mines de Nantes (UMR CNRS 6144 GEPEA), 44 - Nantes (France)

    2004-07-01

    Wastewater treatment plants produce considerable amounts of liquid waste material called sewage sludge. In France, sewage sludge production is about 950,000 tons of dried matter per year. The traditional ways of sludge valorization include farmland application, landfill and incineration. But, with some traditional disposal ways coming under pressure like farmland applications and others being phased out like landfill, it is necessary to seek cost - effective and innovative solutions to sewage sludge disposal problem. Today, one promising approach for production of cheap and efficient carbonaceous sorbent is the use of sewage sludge. This study aims to investigate the effect of sulfuric acid activation conditions on physico-chemical and adsorptive properties of the carbonaceous sorbents made from viscous liquid sludge collected at municipal wastewater treatment plant of Nantes, in France. Chemical activation by sulfuric acid is carried out using an impregnation method. Dried viscous liquid sludge is mixed with H{sub 2}SO{sub 4} solutions for 6 h. The resulting mixture is filtered and dried at 105 C. Then, impregnated sludge is activated in a horizontal furnace under nitrogen atmosphere. The effects of impregnation ratio (0.5 - 1.5 gH{sub 2}SO{sub 4}g{sup -1} sludge), temperature (600-800 C) and time (60-180 minutes) are studied using experimental design methodology. The physico-chemical properties of the resulting sorbents are determined using various characterization techniques: - Elemental analysis, determination of surface functional groups by the Boehm method, surface pH measurement and Point of Zero Charge (pH{sub pzc}) enable a complete characterization of the surface chemistry, - BET analyzer allows specific surface area and the meso-porosity and micro-porosity to be determined. Finally, Adsorption properties are determined during copper ion, dyes (Acid Red 18 and Basic Violet 4) and phenol removal experiments in aqueous solution as well as VOC in gas phase

  20. Characterization of Ru and RuO2 thin films prepared by pulsed metal organic chemical vapor deposition

    International Nuclear Information System (INIS)

    Ultra-thin ruthenium (Ru) layers were fabricated by pulsed metal organic chemical vapor deposition in an Aixtron Tricent reactor using a metal-organic Ru precursor. Layer deposition was performed on different metal barrier combinations and on Al2O3 dielectric layers used in the fabrication of advanced Metal-Insulator-Metal (MIM) capacitor structures and on thermal SiO2 as reference structure. Ru layers with a thickness of 10 nm were characterized by Spectroscopic Ellipsometry (SE) and additional reference methods such as Transmission Electron Microscopy (TEM), Atomic Force Microscopy (AFM), and X-Ray Reflectometry (XRR). As deposited and in situ annealed Ru layers were characterized by SE applying Drude-Lorentz- and Effective Medium Approximation (EMA) models. It was shown that the deposited layers consist of a Ru-RuO2 bilayer structure. By in situ annealing, the RuO2 layer thickness is reduced and highly pure Ru films are obtained. On the metal barriers the formation of a metal oxide interface, which is related to the deposition process, was determined. (copyright 2008 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  1. Characterization of Ru and RuO{sub 2} thin films prepared by pulsed metal organic chemical vapor deposition

    Energy Technology Data Exchange (ETDEWEB)

    Roeder, G.; Petersen, S.; Yanev, V.; Schellenberger, M.; Pfitzner, L.; Ryssel, H. [Fraunhofer Institute of Integrated Systems and Device Technology (IISB), Schottkystrasse 10, Erlangen (Germany); Manke, C.; Baumann, P.K. [AIXTRON AG, Kackertstrasse 15-17, Aachen (Germany); Gschwandtner, A.; Ruhl, G. [Infineon Technologies AG, Wernerwerkstrasse 2, Regensburg (Germany); Petrik, P. [Research Institute for Technical Physics and Materials Science, Konkoly Thege Miklos ut 29-33, Budapest (Hungary)

    2008-05-15

    Ultra-thin ruthenium (Ru) layers were fabricated by pulsed metal organic chemical vapor deposition in an Aixtron Tricent reactor using a metal-organic Ru precursor. Layer deposition was performed on different metal barrier combinations and on Al{sub 2}O{sub 3} dielectric layers used in the fabrication of advanced Metal-Insulator-Metal (MIM) capacitor structures and on thermal SiO{sub 2} as reference structure. Ru layers with a thickness of 10 nm were characterized by Spectroscopic Ellipsometry (SE) and additional reference methods such as Transmission Electron Microscopy (TEM), Atomic Force Microscopy (AFM), and X-Ray Reflectometry (XRR). As deposited and in situ annealed Ru layers were characterized by SE applying Drude-Lorentz- and Effective Medium Approximation (EMA) models. It was shown that the deposited layers consist of a Ru-RuO{sub 2} bilayer structure. By in situ annealing, the RuO{sub 2} layer thickness is reduced and highly pure Ru films are obtained. On the metal barriers the formation of a metal oxide interface, which is related to the deposition process, was determined. (copyright 2008 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  2. Carbon coated Fe3O4 hybrid material prepared by chemical vapor deposition for high performance lithium-ion batteries

    International Nuclear Information System (INIS)

    A hybrid material of carbon coated Fe3O4 (Fe3O4@C) is synthesized by chemical vapor deposition method using Fe2O3 as starting material and acetylene as carbon source. The obtained material is Fe3O4 spheres of ∼400 nm coated by thin carbon layer with a thickness of ∼10 nm. As an anode material for lithium ion batteries, Fe3O4@C shows an improved electrochemical performance in the reversible capacity and cycling stability, together with excellent rate capability. The performance is much better than the results obtained from bare Fe2O3 and commercial Fe3O4 of the same size. In addition to the comparison of electrochemical impedance spectra of the Fe2O3, Fe3O4 and Fe3O4@C electrodes before and after 50 charge/discharge cycles, a surface contrast of the three electrodes before and after cycling is systematically investigated to explore the influence of carbon layer on the electrochemical performance of the Fe3O4 spheres

  3. Preparation of ZrC nano-particles reinforced amorphous carbon composite coating by atmospheric pressure chemical vapor deposition

    International Nuclear Information System (INIS)

    To eliminate cracks caused by thermal expansion mismatch between ZrC coating and carbon-carbon composites, a kind of ZrC/C composite coating was designed as an interlayer. The atmospheric pressure chemical vapor deposition was used as a method to achieve co-deposition of ZrC and C from ZrCl4-C3H6-H2-Ar source. Zirconium tetrachloride (ZrCl4) powder carrier was especially made to control accurately the flow rate. The microstructure of ZrC/C composite coating was studied using analytical techniques. ZrC/C coating shows same morphology as pyrolytic carbon. Transmission electron microscopy (TEM) shows ZrC grains with size of 10-50 nm embed in turbostratic carbon. The formation mechanism is that the growth of ZrC crystals was inhibited by surrounding pyrolytic carbon and kept as nano-particles. Fracture morphologies imply good combination between coating and substrate. The ZrC crystals have stoichiometric proportion near 1, with good crystalline but no clear preferred orientation while pyrolytic carbon is amorphous. The heating-up oxidation of ZrC/C coating shows 11.58 wt.% loss. It can be calculated that the coating consists of 74.04 wt.% ZrC and 25.96 wt.% pyrolytic carbon. The average density of the composite coating is 5.892 g/cm3 by Archimedes' principle.

  4. Identification of higher order long-propagation-length surface plasmon polariton modes in chemically prepared gold nanowires.

    Science.gov (United States)

    Paul, Aniruddha; Solis, David; Bao, Kui; Chang, Wei-Shun; Nauert, Scott; Vidgerman, Leonid; Zubarev, Eugene R; Nordlander, Peter; Link, Stephan

    2012-09-25

    A comprehensive understanding of the type of modes and their propagation length for surface plasmon polaritons (SPPs) in gold nanowires is essential for potential applications of these materials as nanoscale optical waveguides. We have studied chemically synthesized single gold nanowires by a novel technique called bleach-imaged plasmon propagation (BlIPP), which relies on the plasmonic near-field induced photobleaching of a dye to report the SPP propagation in nanowires. We observed a much longer propagation length of 7.5 ± 2.0 μm at 785 nm compared to earlier reports, which found propagation lengths of ~2.5 μm. Finite difference time domain simulations revealed that the bleach-imaged SPP is a higher order m = 1 mode and that the lowest order m = 0 mode is strongly quenched due to the loss to the dye layer and cannot be resolved by BlIPP. A comparative assessment of BlIPP with direct fluorescence imaging furthermore showed that the significant difference in propagation lengths obtained by these two techniques can be attributed to the difference in their experimental conditions, especially to the difference in thickness of the dye layer coating on the nanowire. In addition to identifying a higher order SPP mode with long propagation length, our study infers that caution must be taken in selecting indirect measurement techniques for probing SPP propagation in nanoscale metallic waveguides. PMID:22900780

  5. Vertically aligned Si nanocrystals embedded in amorphous Si matrix prepared by inductively coupled plasma chemical vapor deposition (ICP-CVD)

    International Nuclear Information System (INIS)

    Highlights: • Inductively-coupled plasma is used for nanostructured silicon at room temperature. • Low temperature deposition allows device processing on various substrates. • Deposition pressure is the most effective parameter in controlling nanostructure. • Films consist of quantum dots in a-Si matrix and exhibit columnar vertical growth. • Films are porous to oxygen infusion along columnar grain boundaries. - Abstract: Vertically-aligned nanostructured silicon films are deposited at room temperature on p-type silicon wafers and glass substrates by inductively-coupled, plasma-enhanced chemical vapor deposition (ICPCVD). The nanocrystalline phase is achieved by reducing pressure and increasing RF power. The crystalline volume fraction (Xc) and the size of the nanocrystals increase with decreasing pressure at constant power. Columnar growth of nc-Si:H films is observed by high resolution transmission electron microscopy (HRTEM) and scanning electron microscopy (SEM). The films exhibit cauliflower-like structures with high porosity that leads to slow but uniform oxidation after exposure to air at room temperature. Films deposited at low pressures exhibit photoluminescence (PL) signals that may be deconvoluted into three distinct Gaussian components: 760–810, 920–935, and 990–1000 nm attributable to the quantum confinement and interface defect states. Hydrogen dilution is manifested in significant enhancement of the PL, but it has little effect on the nanocrystal size and Xc

  6. Preparation of Zirconium molybdate gel and evaluation of its physico-chemical characteristics effects on 99mTc generators performances

    International Nuclear Information System (INIS)

    Zirconium molybdate gel has an excellent characteristic to be used as a column matrix material of 99Tc generators. The preparation conditions of zirconium molybdate gels will directly influence their physico-chemical characteristics and thus generator performances. In this work a series of zirconium molybdate gels were synthesized under different conditions and characterized by inductively coupled plasma, thermo gravimetric analysis , XRD and scanning electron microscopy Techniques. The effects of different parameters including p H of molybdate solution, Zr:Mo molar ratios, order of reactants addition, washing and granulating of gel on the performance of technetium-99m generators were evaluated. The experiments show that the optimum conditions for synthesis of the gel consist of: p H=4-4.5, Zr:Mo ratio of 1:1, gradual addition of molybdate solution to zirconium oxy chloride solution, no washing and grinding the resulted gel.

  7. Chemical solution deposition preparation of double-perovskite La2NiMnO6 film on LaAlO3 (0 0 1) substrate

    International Nuclear Information System (INIS)

    The ordered double-perovskite La2NiMnO6 films were successfully deposited on LaAlO3 substrate by chemical solution deposition method. Some La2NiMnO6 films layer with seed layer were also prepared in order to obtain higher quality films. The X-ray diffraction and Raman scattering spectroscopy are used to characterize all the films, it is found that all films are single phase with highly (0 0 l)-oriented. The field-emission scanning electron microscopy shows that the film with seed layer is relatively smooth and dense. The magnetic measurements indicate that all films exhibit a Curie temperature of about 280 K, which is close to that of the bulk material. Moreover, the low temperature magnetization of the films with and without seed layer is different, which can be attributed to that the seed layer can prevent the diffusion between the films and the substrate.

  8. Fast preparation of Na0.44MnO2 nanorods via a high NaOH concentration hydrothermal soft chemical reaction and their lithium storage properties

    International Nuclear Information System (INIS)

    This paper describes a high NaOH concentration hydrothermal soft chemical reaction to prepare Na0.44MnO2 nanorods. In this process, Na-birnessite precursors and concentrated NaOH solution are introduced into the hydrothermal reaction. As a result, the hydrothermal time can be significantly shortened from 96 to 24 h, the hydrothermal temperature can be reduced from 205 to 180 °C and the yield of Na0.44MnO2 can be increased from about 0.6 to about 2.4 g/(mL.day), respectively. Furthermore, the obtained Na0.44MnO2 nanorods with one-dimensional tunnel structures exhibit favorable electrochemical lithium storage properties, which make them promising for the cathode materials of lithium-ion batteries

  9. Preparation of high-quality hydrogenated amorphous silicon film with a new microwave electron cyclotron resonance chemical vapour deposition system assisted with hot wire

    Institute of Scientific and Technical Information of China (English)

    Zhu Xiu-Hong; Chen Guang-Hua; Yin Sheng-Yi; Rong Yan-Dong; Zhang Wen-Li; Hu Yue-Hui

    2005-01-01

    The preparation of high-quality hydrogenated amorphous silicon (a-Si:H) film with a new microwave electron cyclotron resonance-chemical vapour deposition (MWECR-CVD) system assisted with hot wire is presented. In this system the hot wire plays an important role in perfecting the microstructure as well as improving the stability and the optoelectronic properties of the a-Si:H film. The experimental results indicate that in the microstructure of the a-Si:H film, the concentration of dihydride is decreased and a trace of microcrystalline occurs, which is useful to improve its stability, and that in the optoelectronic properties of the a-Si:H film, the deposition rate reaches above 2.0nm/s and the photosensitivity increases up to 4.71× 105.

  10. One-step green synthetic approach for the preparation of multicolor emitting copper nanoclusters and their applications in chemical species sensing and bioimaging.

    Science.gov (United States)

    Bhamore, Jigna R; Jha, Sanjay; Mungara, Anil Kumar; Singhal, Rakesh Kumar; Sonkeshariya, Dhanshri; Kailasa, Suresh Kumar

    2016-06-15

    One-step green microwave synthetic approach was developed for the synthesis of copper nanoclusters (Cu NCs) and used as a fluorescent probe for the sensitive detection of thiram and paraquat in water and food samples. Unexpectedly, the prepared Cu NCs exhibited strong orange fluorescence and showed emission peak at 600nm, respectively. Under optimized conditions, the quenching of Cu NCs emission peak at 600nm was linearly proportional to thiram and paraquat concentrations in the ranges from 0.5 to 1000µM, and from 0.2 to 1000µM, with detection limits of 70nM and 49nM, respectively. In addition, bioimaging studies against Bacillus subtilis through confocal fluorescence microscopy indicated that Cu NCs showed strong blue and green fluorescence signals, good permeability and minimum toxicity against the various bacteria species, which demonstrates their potential feasibility for chemical species sensing and bioimaging applications. PMID:26851582

  11. Preparation of Y-Ba-Cu-O superconducting films on SrTiO3 and MgO substrates by chemical vapor deposition

    International Nuclear Information System (INIS)

    Y-Ba-Cu-O superconducting films were prepared at 850 C by chemical vapor deposition using metal β-diketonates as source materials. The films on SrTiO3(100) and MgO (100) substrates showed c-axis orientation. The degree of c-axis orientation estimated from the rocking curve of the (007) reflection for the film on SrTiO3 was higher than that for the film on MgO. Superconducting transition temperature defined by zero resistivity was 92 K for the films on SrTiO3 and 86 K for the films on MgO. Transport critical-current densities of the films on SrTiO3 and MgO at 77.3 K and O T were 6.0x105 and 8.3x103 A/cm2, respectively

  12. Preparation of Aligned Ultra-long and Diameter-controlled Silicon Oxide Nanotubes by Plasma Enhanced Chemical Vapor Deposition Using Electrospun PVP Nanofiber Template

    Science.gov (United States)

    Zhou, Ming; Zhou, Jinyuan; Li, Ruishan; Xie, Erqing

    2010-02-01

    Well-aligned and suspended polyvinyl pyrrolidone (PVP) nanofibers with 8 mm in length were obtained by electrospinning. Using the aligned suspended PVP nanofibers array as template, aligned ultra-long silicon oxide (SiO x) nanotubes with very high aspect ratios have been prepared by plasma-enhanced chemical vapor deposition (PECVD) process. The inner diameter (20-200 nm) and wall thickness (12-90 nm) of tubes were controlled, respectively, by baking the electrospun nanofibers and by coating time without sacrificing the orientation degree and the length of arrays. The micro-PL spectrum of SiO x nanotubes shows a strong blue-green emission with a peak at about 514 nm accompanied by two shoulders around 415 and 624 nm. The blue-green emission is caused by the defects in the nanotubes.

  13. Physico-chemical properties investigation of cisplatin loaded polybutyladipate (PBA) nanoparticles prepared by w/o/w

    Energy Technology Data Exchange (ETDEWEB)

    Khoee, Sepideh, E-mail: Khoee@khayam.ut.ac.ir [Polymer Chemistry Department, School of Science, University of Tehran, P.O. Box 14155-6455, Tehran (Iran, Islamic Republic of); Sattari, Ahmad [Polymer Chemistry Department, School of Science, University of Tehran, P.O. Box 14155-6455, Tehran (Iran, Islamic Republic of); Atyabi, Fatemeh [Novel Drug Delivery Systems Lab, Faculty of Pharmacy, Medical Sciences/University of Tehran, Tehran P.O. Box 14155-6451 (Iran, Islamic Republic of)

    2012-07-01

    cis-Diamminedichloroplatinum(II) (cisplatin) is used against different kinds of cancers. Unfortunately, because of the severe side-effects like nephrotoxicity, ototoxicity, etc., they are administered in small doses at low concentrations. The purpose of this work is to improve injectional controlled release (ICR) of cisplatin that releases drug in the extended temporal periods. In order to access this aim, biodegradable polymeric nanoparticles containing cisplatin as anticancer drug of various ranges from 71 to 661 nm were prepared by a w/o/w double emulsion solvent evaporation technique. Influences of process parameters such as solvent removal technique, type and concentration of polymer, volume of oil phase, volume of external aqueous phase, concentration of stabilizer, drug concentration in the internal and external aqueous phases and power of sonication on morphology, characteristics of the nanoparticles and release profile were investigated. Morphology of the nanoparticles was studied by transmission electron microscopy (TEM) and scanning electron microscopy (SEM) and the images indicated that spherical shape of the nanoparticles can be tailored to rod-like shape by changing the reaction parameters. Size of the nanoparticles decreased as polymer concentration decreases. Volume of oil phase, power of sonication and drug concentration in the internal water phase affected the size of nanoparticles. Drug release profiles indicate that polymer concentration in the oil phase and stabilizer concentration in the external water phase have critical role in the drug release process from the nanoparticles. The in-vitro release of the encapsulated drug was observed by using the diffusion models of release from a sphere carrier and the release pattern was shown to be a complex process.

  14. Physico-chemical properties investigation of cisplatin loaded polybutyladipate (PBA) nanoparticles prepared by w/o/w

    International Nuclear Information System (INIS)

    cis-Diamminedichloroplatinum(II) (cisplatin) is used against different kinds of cancers. Unfortunately, because of the severe side-effects like nephrotoxicity, ototoxicity, etc., they are administered in small doses at low concentrations. The purpose of this work is to improve injectional controlled release (ICR) of cisplatin that releases drug in the extended temporal periods. In order to access this aim, biodegradable polymeric nanoparticles containing cisplatin as anticancer drug of various ranges from 71 to 661 nm were prepared by a w/o/w double emulsion solvent evaporation technique. Influences of process parameters such as solvent removal technique, type and concentration of polymer, volume of oil phase, volume of external aqueous phase, concentration of stabilizer, drug concentration in the internal and external aqueous phases and power of sonication on morphology, characteristics of the nanoparticles and release profile were investigated. Morphology of the nanoparticles was studied by transmission electron microscopy (TEM) and scanning electron microscopy (SEM) and the images indicated that spherical shape of the nanoparticles can be tailored to rod-like shape by changing the reaction parameters. Size of the nanoparticles decreased as polymer concentration decreases. Volume of oil phase, power of sonication and drug concentration in the internal water phase affected the size of nanoparticles. Drug release profiles indicate that polymer concentration in the oil phase and stabilizer concentration in the external water phase have critical role in the drug release process from the nanoparticles. The in-vitro release of the encapsulated drug was observed by using the diffusion models of release from a sphere carrier and the release pattern was shown to be a complex process.

  15. Preparation of highly photocatalytic active CdS/TiO2 nanocomposites by combining chemical bath deposition and microwave-assisted hydrothermal synthesis

    International Nuclear Information System (INIS)

    CdS/TiO2 nanocomposites were prepared from Cd and Ti (1:1 M ratio) using cetyltrimethylammonium bromide by a two-step chemical bath deposition (CBD) and microwave-assisted hydrothermal synthesis (MAHS) method. A series of nanocomposites with different morphologies and activities were prepared by varying the reaction time in the MAHS (2, 4, and 6 h). The crystal structure, morphology, and surface physicochemical properties of the nanocomposites were characterized by X-ray diffraction, UV–visible diffuse reflectance spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, and N2 adsorption–desorption measurements. The results show that the CdS/TiO2 nanocomposites were composed of anatase TiO2 and hexagonal CdS phases with strong absorption in the visible region. The surface morphologies changed slightly with increasing microwave irradiation time, while the Brunauer–Emmett–Teller surface area increased remarkably. The photocatalytic degradation of methyl orange (MO) was investigated under UV light and simulated sunlight irradiation. The photocatalytic activity of the CdS/TiO2 (6 h) composites prepared by the MAHS method was higher than those of CdS, P25, and other CdS/TiO2 nanocomposites. The CdS/TiO2 (6 h) nanocomposites significantly affected the UV and microwave-assisted photocatalytic degradation of different dyes. To elucidate the photocatalytic reaction mechanism for the CdS/TiO2 nanocomposites, controlled experiments were performed by adding different radical scavengers. - Graphical abstract: CdS/TiO2 nanocomposites were prepared using CTAB by CBD combined with MAHS method. In addition, with increasing microwave irradiation time, the morphology of CdS/TiO2 changed from popcorn-like to wedge-like structure. - Highlights: • The CdS/TiO2 was prepared by CBD combined with MAHS two-step method under CTAB. • The morphologies of as-samples were different with the time of microwave increased. • Compared with TiO2, as-samples show

  16. Preparation of highly photocatalytic active CdS/TiO{sub 2} nanocomposites by combining chemical bath deposition and microwave-assisted hydrothermal synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Li, Li, E-mail: qqhrll@163.com [College of Materials Science and Engineering, Qiqihar University, Qiqihar 161006 (China); Key Laboratory of Composite Modified Material of Colleges in Heilongjiang Province, Qiqihar 161006 (China); Wang, Lili [College of Materials Science and Engineering, Qiqihar University, Qiqihar 161006 (China); Hu, Tianyu [College of Environment and Resources, Jilin University, Changchun 130024 (China); Zhang, Wenzhi; Zhang, Xiuli; Chen, Xi [College of Materials Science and Engineering, Qiqihar University, Qiqihar 161006 (China)

    2014-10-15

    CdS/TiO{sub 2} nanocomposites were prepared from Cd and Ti (1:1 M ratio) using cetyltrimethylammonium bromide by a two-step chemical bath deposition (CBD) and microwave-assisted hydrothermal synthesis (MAHS) method. A series of nanocomposites with different morphologies and activities were prepared by varying the reaction time in the MAHS (2, 4, and 6 h). The crystal structure, morphology, and surface physicochemical properties of the nanocomposites were characterized by X-ray diffraction, UV–visible diffuse reflectance spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, and N{sub 2} adsorption–desorption measurements. The results show that the CdS/TiO{sub 2} nanocomposites were composed of anatase TiO{sub 2} and hexagonal CdS phases with strong absorption in the visible region. The surface morphologies changed slightly with increasing microwave irradiation time, while the Brunauer–Emmett–Teller surface area increased remarkably. The photocatalytic degradation of methyl orange (MO) was investigated under UV light and simulated sunlight irradiation. The photocatalytic activity of the CdS/TiO{sub 2} (6 h) composites prepared by the MAHS method was higher than those of CdS, P25, and other CdS/TiO{sub 2} nanocomposites. The CdS/TiO{sub 2} (6 h) nanocomposites significantly affected the UV and microwave-assisted photocatalytic degradation of different dyes. To elucidate the photocatalytic reaction mechanism for the CdS/TiO{sub 2} nanocomposites, controlled experiments were performed by adding different radical scavengers. - Graphical abstract: CdS/TiO{sub 2} nanocomposites were prepared using CTAB by CBD combined with MAHS method. In addition, with increasing microwave irradiation time, the morphology of CdS/TiO{sub 2} changed from popcorn-like to wedge-like structure. - Highlights: • The CdS/TiO{sub 2} was prepared by CBD combined with MAHS two-step method under CTAB. • The morphologies of as-samples were different with the time of

  17. Preparation and characterization of activated carbon from reedy grass leaves by chemical activation with H3PO4

    International Nuclear Information System (INIS)

    Highlights: • Activated carbons were produced from reedy grass leaves by activation with phosphoric acid. • The activated carbons have a large number of oxygen- and phosphorus-containing surface groups. • The structure of activated carbons was bight fibers features on the surface and the external surface of the activated carbons was slightly corrugated and abundant pores. - Abstract: Activated carbons were produced from reedy grass leaves by chemical activation with H3PO4 in N2 atmosphere and their characteristics were investigated. The effects of activation temperature and time were examined. Adsorption capacity was demonstrated with BET and iodine number. Micropore volume and pore size distribution of activated carbons were characterized by N2 adsorption isotherms. The surface area and iodine number of the activated carbons produced at 500 °C for 2 h were 1474 m2/g and 1128 mg/g, respectively. Thermal decomposition of pure reedy grass leaves and H3PO4-impregnated reedy grass leaves have been investigated with thermogravimetric/mass spectroscopy (TG–MS) technique. It was found that the temperature and intensity of maximum evolution of H2O and CO2 of H3PO4-impregnated reedy grass leaves were lower than that of pure reedy grass leaves. This implies that H3PO4 as an activating reagent changed the thermal degradation of the reedy grass leaves, stabilized the cellulose structure, leading to a subsequent change in the evolution of porosity. The results of X-ray photoelectron spectroscopy and Fourier-infrared spectroscopy analysis indicate that the produced activated carbons have rich functional groups on surface

  18. The effect of thermal annealing on the optical band gap of cadmium sulphide thin films, prepared by the chemical bath deposition technique

    International Nuclear Information System (INIS)

    Cadmium sulphide thin films have been prepared by the chemical bath deposition technique (ph 11, 70 degree centigrade). Two different sets of films were prepared under varied conditions and concentrations of their ions sources (Cd2+ from cadmium nitrate, S2- from thiourea) and Na2EDTA as a complexing agent. A UV mini-Schimazu UV-VIS Spectrophotometer was used to determine the optical absorbance of the films as a function of wavelength at room temperature over the wavelength range 200 - 600 nm. The samples were then thermally annealed for thirty minutes, at temperatures of 100 degree centigrade, and 200 degree centigrade, after which the absorbance of the films were again recorded. The band gap values obtained for the sample with 0.5 M CdS as deposited, annealed at 100 degree centigrade and 200 degree centigrade were 2.1 eV, 2.2 eV and 2.3 eV respectively. Whilst the values obtained for the sample 0.15 CdS as deposited, annealed at 100 degree centigrade and annealed at 200 degree centigrade were 2.0 eV, 2.01 eV and 2.02 eV respectively. The increase in band gap with annealing temperature might be attributed to the improvement in crystallinity in the films. (au)

  19. Rare earths: preparation of spectro chemically pure standards, study of their carbonates and synthesis of a new compound series - the peroxy carbonates

    International Nuclear Information System (INIS)

    In this work the following studies are concerned: I) preparation of lanthanum, cerium, praseodymium, neodymium and samarium oxides for use as spectro chemically pure standards; II) behavior of the rare earth (La, Ce, Pr, Nd, Sm) carbonates soluble in ammonium carbonate and mixture of ammonium carbonate/ammonium hydroxide, and III) synthesis and characterization of rare earth peroxy carbonates - a new series of compounds. Data for the synthesis and characterization of the rare earths peroxy carbonates described for the first time in this work are presented and discussed. With the aid of thermal analysis (TG-DTG) the thermal stability and the stoichiometric composition for new compounds were established and a mechanism of thermal decomposition was proposed. The peroxy carbonate was prepared by the addition of hydrogen peroxyde to the complexed soluble rare earths carbonates. These studies included also the determinations of active oxygen, the total rare earth oxide by gravimetry and complexometry and the C, H and N contents by microanalysis. The new compounds were also investigated by infrared spectroscopy. (author)

  20. Effect of glass tempering on microstructure and functional properties of SnO2:F thin film prepared by atmosphere pressure chemical vapor deposition

    International Nuclear Information System (INIS)

    The low-emission glass was prepared via depositing fluorine-doped tin oxide thin film on glass substrate by atmospheric pressure chemical vapor deposition method. The as-deposited low-emission glass was found to present a SnO2:F/SiCxOy/glass sandwich structure via focused ion beam technique and transmission microscopic measurement. After tempering process at ∼ 650 °C with varied periods, the electrical and optical properties of the SnO2:F thin film remained stable for less than 10 min, but decreased dramatically when the tempering period exceeded 10 min, which was mainly due to the oxygen chemisorptions and fluorine ion diffusion. It was observed that the SnO2:F thin films presented uniform polycrystalline nature of cassiterite structure throughout the tempering process. The study has therefore suggested the appropriate tempering conditions for the SnO2:F low-emission glass, and provided a critical guidance for further energy-saving glass applications. - Highlights: • The sandwich structural low-e glass was prepared on an industrial line. • The film showed stable morphology and functional property under low temperature. • The functional property decreased dramatically after long time tempering at 650 °C

  1. Fibrous TiO2 prepared by chemical vapor deposition using activated carbon fibers as template via adsorption, hydrolysis and calcinations

    Institute of Scientific and Technical Information of China (English)

    Hui-na YANG; Li-fen LIU; Feng-lin YANG; Jimmy C. YU

    2008-01-01

    TiO2 fibers were prepared via alternatively introducing water vapor and Ti precursor carried by Ne to an APCVD (chemical vapor deposition under atmospheric pressure) reactor at <200 ℃. Activated carbon fibers (ACFs) were used as templates for deposition and later removed by calcinations. The obtained catalysts were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), Brtmauer, Emmett and Teller (BET) and X-ray diffraction (XRD) analysisThe pores within TiO2 fibers included micro-range and meso-range, e.g., 7 nm, and the specific surface areas for TiO2 fibers were 141 m2/g and 148 m2/g for samples deposited at 100 ℃ and 200 ℃ (using ACF1700 as template), respectively. The deposition temperature significantly influenced TiO2 morphology. The special advantages of this technique for preparing porous nano-material include no consumption of organic solvent in the process and easy control of deposition conditions and speeds.

  2. Aqueous Chemical Solution Deposition of Novel, Thick and Dense Lattice-Matched Single Buffer Layers Suitable for YBCO Coated Conductors: Preparation and Characterization

    Directory of Open Access Journals (Sweden)

    Isabel van Driessche

    2012-09-01

    Full Text Available In this work we present the preparation and characterization of cerium doped lanthanum zirconate (LCZO films and non-stoichiometric lanthanum zirconate (LZO buffer layers on metallic Ni-5% W substrates using chemical solution deposition (CSD, starting from aqueous precursor solutions. La2Zr2O7 films doped with varying percentages of Ce at constant La concentration (La0.5CexZr1−xOy were prepared as well as non-stoichiometric La0.5+xZr0.5−xOy buffer layers with different percentages of La and Zr ratios. The variation in the composition of these thin films enables the creation of novel buffer layers with tailored lattice parameters. This leads to different lattice mismatches with the YBa2Cu3O7−x (YBCO superconducting layer on top and with the buffer layers or substrate underneath. This possibility of minimized lattice mismatch should allow the use of one single buffer layer instead of the current complicated buffer architectures such as Ni-(5% W/LZO/LZO/CeO2. Here, single, crack-free LCZO and non-stoichiometric LZO layers with thicknesses of up to 140 nm could be obtained in one single CSD step. The crystallinity and microstructure of these layers were studied by XRD, and SEM and the effective buffer layer action was studied using XPS depth profiling.

  3. The Synthesis of Anatase Nanoparticles and the Preparation of Photocatalytically Active Coatings Based on Wet Chemical Methods for Self-Cleaning Applications

    Directory of Open Access Journals (Sweden)

    Dejan Verhovšek

    2012-01-01

    Full Text Available We report on an improved sol-gel method for the production of highly photocatalytic titanium dioxide (TiO2 anatase nanoparticles which can provide appropriate control over the final characteristics of the nanoparticles, such as particle size, crystallinity, crystal structure, morphology, and also the degree of agglomeration. The synthesized anatase nanoparticles were characterized using various techniques, such as X-ray powder diffraction (XRD, scanning electron microscopy (SEM, and transmission electron microscopy (TEM, and were tested in coatings for self-cleaning glass and ceramic surfaces. The coatings were prepared using a soft chemistry route and are completely transparent to visible light and exhibit a high photocatalytic effect, which was determined by contact-angle measurements. Finally, it is worth mentioning that both the sol-gel synthesis method and the coating-preparation method are based on a wet chemical process, thus presenting no risk of handling the TiO2 anatase nanoparticles in their potentially hazardous powder form at any stage of our development. Low-price, easy-to-handle, and nontoxic materials were used. Therefore, our work represents an important contribution to the development of TiO2 anatase nanoparticle coatings that provide a high photocatalytic effect and can thus be used for numerous applications.

  4. Effect of glass tempering on microstructure and functional properties of SnO{sub 2}:F thin film prepared by atmosphere pressure chemical vapor deposition

    Energy Technology Data Exchange (ETDEWEB)

    Gao, Qian [State Key Laboratory for Silicon Materials and Center for Electron Microscopy, Department of Materials Science and Engineering, Zhejiang University, Hangzhou, 310027 (China); Liu, Qiying [Hangzhou Bluestar New Materials Technology Co., Ltd, Hangzhou, 310012 (China); Li, Ming [State Key Laboratory for Silicon Materials and Center for Electron Microscopy, Department of Materials Science and Engineering, Zhejiang University, Hangzhou, 310027 (China); Li, Xiang, E-mail: xiang.li@zju.edu.cn [State Key Laboratory for Silicon Materials and Center for Electron Microscopy, Department of Materials Science and Engineering, Zhejiang University, Hangzhou, 310027 (China); Liu, Yong; Song, Chenlu; Wang, Jianxun [State Key Laboratory for Silicon Materials and Center for Electron Microscopy, Department of Materials Science and Engineering, Zhejiang University, Hangzhou, 310027 (China); Liu, Junbo [Hangzhou Bluestar New Materials Technology Co., Ltd, Hangzhou, 310012 (China); Shen, Ge [State Key Laboratory for Silicon Materials and Center for Electron Microscopy, Department of Materials Science and Engineering, Zhejiang University, Hangzhou, 310027 (China); Han, Gaorong, E-mail: hgr@zju.edu.cn [State Key Laboratory for Silicon Materials and Center for Electron Microscopy, Department of Materials Science and Engineering, Zhejiang University, Hangzhou, 310027 (China)

    2013-10-01

    The low-emission glass was prepared via depositing fluorine-doped tin oxide thin film on glass substrate by atmospheric pressure chemical vapor deposition method. The as-deposited low-emission glass was found to present a SnO{sub 2}:F/SiC{sub x}O{sub y}/glass sandwich structure via focused ion beam technique and transmission microscopic measurement. After tempering process at ∼ 650 °C with varied periods, the electrical and optical properties of the SnO{sub 2}:F thin film remained stable for less than 10 min, but decreased dramatically when the tempering period exceeded 10 min, which was mainly due to the oxygen chemisorptions and fluorine ion diffusion. It was observed that the SnO{sub 2}:F thin films presented uniform polycrystalline nature of cassiterite structure throughout the tempering process. The study has therefore suggested the appropriate tempering conditions for the SnO{sub 2}:F low-emission glass, and provided a critical guidance for further energy-saving glass applications. - Highlights: • The sandwich structural low-e glass was prepared on an industrial line. • The film showed stable morphology and functional property under low temperature. • The functional property decreased dramatically after long time tempering at 650 °C.

  5. Preparation of core–shell porous magnetite@carbon nanospheres through chemical vapor deposition as anode materials for lithium-ion batteries

    International Nuclear Information System (INIS)

    Highlights: • Fe3O4/C composites are prepared through hydrothermal treatment and subsequent CVD. • Monodispersed core–shell Fe3O4@C nanospheres are connected with 3D carbon networks. • Fe3O4@C composites exhibit high reversible capacity and excellent rate capability. - Abstract: Monodispersed core-shell porous Fe3O4@C nanospheres are prepared through hydrothermal treatment and subsequent chemical vapor deposition (CVD). Specially, the magnetite reduction and carbon coating are completed via CVD simultaneously and the process is verified by X-ray diffraction, scanning electron microscope and transmission electron microscope. Fe3O4@C composites exhibit high reversible capacity (∼1100 mA h g−1 at 100 mA g−1 after 60 cycles), excellent cyclic stability and good rate performance. The carbon coating layer serves as a highly conducting framework and provides a flexible space for buffering strain and stress, and the pores facilitate ion transport during electrochemical cycling. More importantly, the core-shell Fe3O4@C composite is connected by carbon to form a three-dimensional network, which contributes to the relief of inner strain and the fast transport of electrons and lithium ions

  6. Optimization of Preparation of Activated Carbon from Ricinus communis Leaves by Microwave-Assisted Zinc Chloride Chemical Activation: Competitive Adsorption of Ni2+ Ions from Aqueous Solution

    Directory of Open Access Journals (Sweden)

    M. Makeswari

    2013-01-01

    Full Text Available The preparation of activated carbon (AC from Ricinus communis leaves was investigated in this paper. Orthogonal array experimental design method was used to optimize the preparation of AC using microwave assisted zinc chloride. Optimized parameters were radiation power of 100 W, radiation time of 8 min, concentration of zinc chloride of 30% by volume, and impregnation time of 24 h, respectively. The surface characteristics of the AC prepared under optimized conditions were examined by pHZPC, SEM-EDAX, XRD, and FTIR. Competitive adsorption of Ni2+ ions on Ricinus communis leaves by microwave assisted zinc chloride chemical activation (ZLRC present in binary and ternary mixture was compared with the single metal solution. The effects of the presence of one metal ion on the adsorption of the other metal ion were investigated. The experimental results indicated that the uptake capacity of one metal ion was reduced by the presence of the other metal ion. The extent of adsorption capacity of the binary and ternary metal ions tested on ZLRC was low (48–69% as compared to single metal ions. Comparisons with the biosorption of Ni2+ ions by the biomass of ZLRC in the binary (48.98–68.41%-~Ni-Cu and 69.76–66.29%-~Ni-Cr and ternary solution (67.32–57.07%-~Ni–Cu and Cr could lead to the conclusion that biosorption of Ni2+ ions was reduced by the influence of Cu2+ and Cr3+ ions. The equilibrium data of the adsorption was well fitted to the Langmuir isotherm. The adsorption process follows the pseudo-second-order kinetic model.

  7. Improved ferroelectric polarization of V-doped Bi6Fe2Ti3O18 thin films prepared by a chemical solution deposition

    International Nuclear Information System (INIS)

    We prepared V-doped Bi6Fe2Ti3O18 thin films on Pt/Ti/SiO2/Si (100) substrates by using a chemical solution deposition route and investigated the doping effect on the microstructure, dielectric, leakage, and ferroelectric properties of Bi6Fe2Ti3O18 thin films. The Bi5.97Fe2Ti2.91V0.09O18 thin film exhibits improved dielectric properties, leakage current, and ferroelectric properties. The incorporation of vanadium resulted in a substantially enhanced remnant polarization (2Pr) over 30 μC/cm2 in Bi5.97Fe2Ti2.91V0.09O18 thin film compared with 10 μC/cm2 in Bi6Fe2Ti3O18 thin film. It is demonstrated that the improved properties may stem from the improvement of crystallinity of the films with the contribution of suppressed oxygen vacancies and decreased mobility of oxygen vacancies caused by the V-doping. The results will provide a guidance to optimize the ferroelectric properties in Bi6Fe2Ti3O18 thin films by chemical solution deposition, which is important to further explore single-phase multiferroics in the n = 5 Aurivillius thin films

  8. Multi-element trace determinations in pure alkaline earth fluoride powders by high-resolution ICP-MS using wet-chemical sample preparation and laser ablation

    Energy Technology Data Exchange (ETDEWEB)

    Tibi, Markus; Heumann, Klaus G. [Institute of Inorganic Chemistry and Analytical Chemistry, Johannes Gutenberg-University Mainz, Duesbergweg 10-14, 55099, Mainz (Germany)

    2003-09-01

    Four alternative analytical procedures for the determination of ten important trace impurities (Mg, Cr, Fe, Cu, Zn, Sr, Zr, Cd, Ba, and Pb) in pure alkaline earth fluoride powders were applied using high-resolution inductively coupled plasma mass spectrometry (ICP-MS). Two procedures are based on a wet-chemical microwave digestion with boric acid and quantification by the standard addition technique and isotope dilution mass spectrometry (IDMS), respectively. In addition, analyses are also performed by laser ablation as a direct solid sampling technique applying matrix-matched external calibration as well as isotope dilution of the powdered sample. For most elements good agreement between the different methods is found. Detection limits for laser ablation vary between 0.05 ng g{sup -1} for Zr and 20 ng g{sup -1} for Mg. They are about one to two orders of magnitude lower than those of the wet-chemical procedures, which is mainly due to the high dilution factor during the sample preparation step. Advantages and restrictions of the different analytical procedures are discussed with respect to their routine applicability. Due to its relatively high accuracy, low detection limits, and time-efficiency LA-ICP-IDMS is the preferred choice if no standard reference materials are available. (orig.)

  9. The isotype ZnO/SiC heterojunction prepared by molecular beam epitaxy--A chemical inert interface with significant band discontinuities.

    Science.gov (United States)

    Zhang, Yufeng; Lin, Nanying; Li, Yaping; Wang, Xiaodan; Wang, Huiqiong; Kang, Junyong; Wilks, Regan; Bär, Marcus; Mu, Rui

    2016-01-01

    ZnO/SiC heterojunctions show great potential for various optoelectronic applications (e.g., ultraviolet light emitting diodes, photodetectors, and solar cells). However, the lack of a detailed understanding of the ZnO/SiC interface prevents an efficient and rapid optimization of these devices. Here, intrinsic (but inherently n-type) ZnO were deposited via molecular beam epitaxy on n-type 6H-SiC single crystalline substrates. The chemical and electronic structure of the ZnO/SiC interfaces were characterized by ultraviolet/x-ray photoelectron spectroscopy and x-ray excited Auger electron spectroscopy. In contrast to the ZnO/SiC interface prepared by radio frequency magnetron sputtering, no willemite-like zinc silicate interface species is present at the MBE-ZnO/SiC interface. Furthermore, the valence band offset at the abrupt ZnO/SiC interface is experimentally determined to be (1.2 ± 0.3) eV, suggesting a conduction band offset of approximately 0.8 eV, thus explaining the reported excellent rectifying characteristics of isotype ZnO/SiC heterojunctions. These insights lead to a better comprehension of the ZnO/SiC interface and show that the choice of deposition route might offer a powerful means to tailor the chemical and electronic structures of the ZnO/SiC interface, which can eventually be utilized to optimize related devices. PMID:26976240

  10. 工业双戊烯在精细化学品制备中的应用%Application of industrial dipentene in preparation of fine chemicals

    Institute of Scientific and Technical Information of China (English)

    苗雨欣; 蒋丽虹; 王昊; 王亚明

    2011-01-01

    介绍了工业双戊烯的来源、组成和物理化学性质.从双戊烯合成香料、催化加氢合成对盖烷、双戊烯合成萜烯马来酸酐加合物、双戊烯脱氢合成对伞花烃等4个方面综述了工业双戊烯在精细化学品制备中的应用情况;分析总结了国内外的研究进展、合成方法及反应条件;并提出了解决双戊烯工业化问题的有效途径.%Sources, composition, as well as physical and chemical properties of industrial dipentene were described. Applications of industrial dipentene in manufacture of fine chemicals were summarized as four categories, namely: synthesis of aroma compounds, synthesis of p - menthane through catalytic hydrogenation,preparation of terpene maleic anhydride adducts and synthesis of p- eymene through dipentene dehydrogenation. Progress in research work with respect to methods for synthesis and reaction conditions for making the above mentioned products were presented. Effective way to get industrial dipentene on a commercial scale was proposed.

  11. Photocatalytic removal of hazardous Ponceau S dye using Nano structured Ni-doped TiO2 thin film prepared by chemical method

    Science.gov (United States)

    Marathe, Sunil D.; Shrivastava, Vinod S.

    2015-02-01

    Many attempts have been made by researchers for the removal of various dyes using nano structured Ni-doped TiO2; however, removal of `hazardous Ponceau S dye' using nano structured Ni-doped TiO2 has been not studied yet. In the present work, environmental application of Nano structured Ni doped TiO2 has been studied. Nano structured Ni-doped TiO2 thin films were deposited by the chemical method on a glass substrate. The prepared thin film was characterized by XRD, SEM, and EDX. The crystal size calculated from XRD is about 26.2 nm. The SEM analysis reveals nano spherical morphology of average particle size about 92 nm. The optical analysis was carried by using UV-visible spectroscopy. The band gap estimated from absorbance spectra for thin film was around 3.5 eV, making suitable Ni-doped TiO2 for photocatalytic removal of hazardous Ponceau S dye. In photocatalytic application different parameters like dye concentration, contact time, pH, UV light and sunlight were optimized for the removal of Ponceau S dye, respectively. The change in chemical oxygen demand after photo catalytic treatment was also studied.

  12. Characterization of CuInS2 thin films prepared by chemical bath deposition and their implementation in a solar cell

    International Nuclear Information System (INIS)

    CuInS2 thin films were formed by the sequential deposition of In2S3–CuS layers on glass substrates, by chemical bath deposition technique, and heating these multilayer 1 h at 350 °C and 400 mPa. The morphology and thickness of the CuInS2 thin films were analysed by scanning electron microscopy, showing particles with elongated shape and length about 40 nm, and thickness of 267 and 348 nm for samples from 15 and 24 h of deposition time in the chemical bath of In2S3, respectively. The energy band gap values of the films were around 1.4 eV, whereas the electrical conductivity showed values from 64.91 to 4.11 × 10−3 Ω−1 cm−1 for the samples of 15 and 24 h of In2S3 deposition bath, respectively. The obtained CuInS2 films showed appropriate values for their application as an absorbing layer in photovoltaic structures of the type: glass/SnO2:F/CdS/Sb2S3/CuInS2/PbS/C/Ag. The whole structure was obtained through chemical bath deposition technique. The solar cell corresponding to 15 h of In2S3 deposition duration bath showed energy-conversion efficiency (η) of 0.53% with open circuit voltage (Voc) of 530 mV, short circuit current density (Jsc) of 2.43 mA cm−2, and fill factor (FF) of 0.41. In the case of the structure with 24 h of deposition of In2S3 bath, η = 0.43% was measured with the following parameters: Voc = 330 mV, Jsc = 4.78 mA cm−2 and FF = 0.27. - Highlights: • CuInS2 films were formed by chemical bath deposition followed by a heat treatment. • Prepared CuInS2 thin films can work as an effective absorbing layer in a solar cell. • A complete solar cell structure was made by a chemical bath deposition method

  13. Characterization of CuInS{sub 2} thin films prepared by chemical bath deposition and their implementation in a solar cell

    Energy Technology Data Exchange (ETDEWEB)

    Lugo, S.; López, I. [Universidad Autónoma de Nuevo León, UANL, Facultad de Ciencias Químicas, Laboratorio de Materiales I, Av. Universidad, Cd. Universitaria 66451, San Nicolás de los Garza, Nuevo León, México (Mexico); Peña, Y., E-mail: yolapm@gmail.com [Universidad Autónoma de Nuevo León, UANL, Facultad de Ciencias Químicas, Laboratorio de Materiales I, Av. Universidad, Cd. Universitaria 66451, San Nicolás de los Garza, Nuevo León, México (Mexico); Calixto, M. [Instituto de Energías Renovables, Universidad Nacional Autónoma de México, C.P. 62580, Temixco, Morelos, México (Mexico); Hernández, T. [Universidad Autónoma de Nuevo León, UANL, Facultad de Ciencias Químicas, Laboratorio de Materiales I, Av. Universidad, Cd. Universitaria 66451, San Nicolás de los Garza, Nuevo León, México (Mexico); Messina, S. [Universidad Autónoma de Nayarit, Ciudad de la Cultura “Amado Nervo”, S/N C.P. 63155, Tepic, Nayarit, México (Mexico); and others

    2014-10-31

    CuInS{sub 2} thin films were formed by the sequential deposition of In{sub 2}S{sub 3}–CuS layers on glass substrates, by chemical bath deposition technique, and heating these multilayer 1 h at 350 °C and 400 mPa. The morphology and thickness of the CuInS{sub 2} thin films were analysed by scanning electron microscopy, showing particles with elongated shape and length about 40 nm, and thickness of 267 and 348 nm for samples from 15 and 24 h of deposition time in the chemical bath of In{sub 2}S{sub 3}, respectively. The energy band gap values of the films were around 1.4 eV, whereas the electrical conductivity showed values from 64.91 to 4.11 × 10{sup −3} Ω{sup −1} cm{sup −1} for the samples of 15 and 24 h of In{sub 2}S{sub 3} deposition bath, respectively. The obtained CuInS{sub 2} films showed appropriate values for their application as an absorbing layer in photovoltaic structures of the type: glass/SnO{sub 2}:F/CdS/Sb{sub 2}S{sub 3}/CuInS{sub 2}/PbS/C/Ag. The whole structure was obtained through chemical bath deposition technique. The solar cell corresponding to 15 h of In{sub 2}S{sub 3} deposition duration bath showed energy-conversion efficiency (η) of 0.53% with open circuit voltage (V{sub oc}) of 530 mV, short circuit current density (J{sub sc}) of 2.43 mA cm{sup −2}, and fill factor (FF) of 0.41. In the case of the structure with 24 h of deposition of In{sub 2}S{sub 3} bath, η = 0.43% was measured with the following parameters: V{sub oc} = 330 mV, J{sub sc} = 4.78 mA cm{sup −2} and FF = 0.27. - Highlights: • CuInS{sub 2} films were formed by chemical bath deposition followed by a heat treatment. • Prepared CuInS{sub 2} thin films can work as an effective absorbing layer in a solar cell. • A complete solar cell structure was made by a chemical bath deposition method.

  14. TiO{sub 2} based photo-catalysts prepared by chemical vapor infiltration (CVI) on micro-fibrous substrates; Photocatalyseurs a base de TiO{sub 2} prepares par infiltration chimique en phase vapeur (CVI) sur supports microfibreux

    Energy Technology Data Exchange (ETDEWEB)

    Sarantopoulos, Ch

    2007-10-15

    This thesis deals with micro-fibrous glass substrates functionalized with TiO{sub 2}. The oxide is deposited as a thin film onto the micro fibres by chemical vapour infiltration (CVI), yielding a photo-catalytic material usable for cleaning polluted air. We studied the relation between the structure of the material and its photo-catalytic efficiency. TiO{sub 2} thin films were prepared at low pressure, in a hot-wall CVD reactor, using Ti(O-iPr){sub 4} as a precursor. They were characterized by XRD, SEM, EDX, XPS and BET, and by recording the kinetics of decomposition of varied pollutants in solution (orange G, malic acid, imazapyr) and in air (toluene). The conditions favoring the growth of porous films through a columnar growth mode were established by MOCVD-depositing TiO{sub 2} thin films on flat substrates. The subsequent works with micro fibrous thick substrates showed the uniformity of infiltration to be the main factor governing the photo-catalytic efficiency. Operating parameters that optimize infiltration do not yield columnar growth mode. A compromise is necessary. Our photo-catalysts are showing high efficiency comparable, if not higher, to those actually commercialized. These promising results are opening real perspectives for the proposed process. (author)

  15. A Novel Strategy for Preparation of Si-HA Coatings on C/C Composites by Chemical Liquid Vaporization Deposition/Hydrothermal Treatments

    Science.gov (United States)

    Xin-Bo, Xiong; Xin-Ye, Ni; Ya-Yun, Li; Cen-Cen, Chu; Ji-Zhao, Zou; Xie-Rong, Zeng

    2016-08-01

    A novel strategy for the preparation of Si-doped hydroxyapatite (Si-HA) coatings on H2O2-treated carbon/carbon composites (C/C) was developed. HA coating was prepared on C/C through chemical liquid vaporization deposition (CLVD)/hydrothermal treatment. HA coating was immersed in an H2SiO3 solution at an autoclave at 413 K for transformation into Si-HA coating. The effects of H2SiO3 mass contents on the phase, morphology, and composition of the Si-HA coatings were studied through SEM, EDS,XRD, and FTIR. Their bonding performance to C/C was measured through a scratch test. Under the optimal content condition, the in vitro skull osteoblast response behaviors of the Si-HA coating were evaluated. Results showed that SiO32‑ could enter into the HA lattice and occupy the PO43‑ sites. Doped SiO32‑ significantly improved the bonding performance of the HA coating to C/C in comparison with the untreated HA. The adhesive strength of the coatings initially increased and then decreased with increasing H2SiO3 content. Meanwhile, the cohesive strength of the Si-HA coatings was almost nearly identical. The Si-HA coating achieved at a content of 90% H2SiO3 exhibited the best bonding performance, and its osteoblast compatibility in vitro was superior to that of the untreated HA coating on C/C through CLVD/hydrothermal treatment.

  16. Effect of thermal annealing on the structural and mechanical properties of amorphous silicon carbide films prepared by polymer-source chemical vapor deposition

    International Nuclear Information System (INIS)

    We report on the effect of thermal annealing on the structural and mechanical properties of amorphous SiC thin films prepared by means of a polymer-source chemical vapor deposition process. The chemical bondings of the a-SiC:H films were systematically examined by means of Fourier transform infrared spectroscopy (FTIR). The film composition was measured by X-ray photoelectron spectroscopy, while X-ray reflectivity measurements were used to account for the film density variations caused by the post-annealing treatments over the 750-1200 oC range. In addition, their mechanical properties (hardness and Young's modulus) were investigated by using the nano-indentation technique. FTIR measurements revealed that not only the intensity of a-SiC absorption band linearly increases but also its position is found to shift to a higher wave number as a result of annealing. In addition, the bond density of Si-C is found to increase from (101.6-224.5) x 1021 bond.cm-3 accompanied by a decrease of Si-H bond density from (2.58-0.46)x 1021 bond.cm-3 as a result of increasing the annealing temperature (Ta) from 750 to 1200 oC. Annealing-induced film densification is confirmed, as the a-SiC film density is found to increase from 2.36 to ∼ 2.75 g/cm-3 when Ta is raised from 750 to 1200 oC. In addition, as Ta is increased from 750 to 1200 oC, both hardness and Young's modulus are found to increase from 15.5 to 17.6 GPa and 155 to 178 GPa, respectively. Our results confirm the previously established linear correlation between the mechanical properties of the a-SiC films and their bond densities.

  17. Preparation of activated carbons from walnut shells by vacuum chemical activation%核桃壳真空化学活化制备活性炭

    Institute of Scientific and Technical Information of China (English)

    杨娟; 丘克强

    2012-01-01

    Activated carbons were prepared from walnut shells by vacuum chemical activation. The effects of system pressure, activation temperature and impregnation ratio on the properties (BET surface area, pore size distribution, iodine and methylene blue adsorption values, and surface characteristics) of activated carbon were studied. The results show that the BET surface area and total pore volume of activated carbon obtained at system pressure of 30 kPa have increased by 27% and 25% respectively compared with those of activated carbon prepared under atmospheric condition. Vacuum condition is beneficial to develop microporous structure, and mesopore tends to be well developed at high impregnation ratio. The activated carbon prepared at system pressure of 30 kPa, activation temperature of 450 ℃, and impregnation ratio of 2.0, possesses a BET surface area of 1 800 m2/g, a total pore volume of 1.176 cm3/g, an iodine adsorption value of 1 050 mg/'g. a methylene blue adsorption value of 315 mg/g and an isoelectric point of 9.15.%采用真空化学活化法,以核桃壳为原料,氯化锌为活化剂制备活性炭,探讨体系压力、活化温度、浸渍比对活性炭比表面积、孔径分布、碘值和亚甲基蓝值以及表面性质的影响.研究结果表明,30 kPa时制备的活性炭其比表面积和总孔体积比常压条件时分别提高了27%和25%;在低压条件下有利于微孔的形成,在高浸渍比的条件下有利于中孔的形成.在体系压力为30 kPa,活化温度为450℃,浸渍比为2.0时,所得活性炭的BET比表面积为1800 m2/g,总孔体积为1.176 cm3/g,等电点为9.15,碘吸附量为1050 mg/g,亚甲基蓝吸附量为315 mg/g.

  18. Size effect and enhanced photocatalytic activity of CuO sheet-like nanostructures prepared by a room temperature solution phase chemical method

    International Nuclear Information System (INIS)

    Size effect and photocatalytic activity of CuO sheet-like nanostructures, which were synthesized by a facile solution phase chemical method with ethanol and water mixture as solvent, have been investigated by UV–vis absorption spectrum and photocatalytic degradation of pollutant rhodamine B (RhB). UV–vis absorption spectrum indicated that the band gap energy was about 2.31 eV for the as-prepared CuO nanostructures. The result indicates that the band gap energy of the CuO sheet-like nanostructures is much larger than value of bulk CuO crystals, showing that the CuO sheet-like nanostructures exhibit a strong quantum size confinement effect. The photocatalytic activity indicates that the as-synthesized CuO sheet-like nanostructures show an enhanced photocatalytic activity with 96.7% degradation of RhB after 9 h reaction under UV light irradiation, which was much higher than that of commercial CuO powders (39.6%).

  19. Post deposition annealing temperature effect on silicon quantum dots embedded in silicon nitride dielectric multilayer prepared by hot-wire chemical vapor deposition

    International Nuclear Information System (INIS)

    The preparations of the 20-period of a Si quantum dot (QD)/SiNx multilayer in a hot-wire chemical vapor deposition (HWCVD) chamber is presented in this paper. The changes in the properties of Si-QDs after the post deposition annealing treatment are studied in detail. Alternate a-Si:H and SiNx layers are grown in a single SiNx deposition chamber by cracking SiH4, and SiH4 + NH3, respectively at 250 oC. The as-deposited samples are annealed in the temperature range of 800 oC to 950 oC to grow Si-QDs. All the samples are characterized by confocal micro Raman, transmission electron microscope (TEM), and photoluminescence (PL) to study the changes in the film structures after the annealing treatment. The micro Raman analysis of the samples shows the frequency line shifting from 482 cm-1 to 500 cm-1 indicating the Si transition from an amorphous to a crystalline phase. The TEM micrograph inspection indicates the formation of Si-QDs of size 3 to 5 nm and a density of 5 x 1012/cm2. The high resolution TEM micrographs show an agglomeration of Si-QDs with an increase in the annealing temperature. The PL spectra show a peak shifting from 459 nm to 532 nm with increasing the annealing temperature of the film.

  20. Removal of Zn(II) and Hg(II) from aqueous solution on a carbonaceous sorbent chemically prepared from rice husk

    International Nuclear Information System (INIS)

    A carbonaceous sorbent was prepared from rice husk via sulfuric acid treatment. Sorption of Zn(II) and Hg(II) from aqueous solution was studied varying time, pH, metal concentration, temperature and sorbent status (wet and dry). Zn(II) sorption was found fast reaching equilibrium within ∼2 h while Hg(II) sorption was slow reaching equilibrium within ∼120 h with better performance for the wet sorbent than for the dry. Kinetics data for both metals were found to follow pseudo-second order model. Sorption rate of both metals was enhanced with temperature rise. Activation energy, Ea, for Zn(II) sorption, was ∼13.0 kJ/mol indicating a diffusion-controlled process ion exchange process, however, for Hg(II) sorption, Ea was ∼54 kJ/mol indicating a chemically controlled process. Sorption of both metals was low at low pH and increased with pH increase. Sorption was much higher for Hg(II) than for Zn(II) with higher uptake for both metals by rising the temperature. Hg(II) was reduced to Hg(I) on the sorbent surface. This was confirmed from the identification of Hg2Cl2 deposits on the sorbent surface by scanning electron microscopy and X-ray diffraction. However, no redox processes were observed in Zn(II) sorption. Sorption mechanism is discussed.

  1. Preparation of monodisperse polystyrene/silica core-shell nano-composite abrasive with controllable size and its chemical mechanical polishing performance on copper

    International Nuclear Information System (INIS)

    Monodisperse silica-coated polystyrene (PS) nano-composite abrasives with controllable size were prepared via a two-step process. Monodisperse positively charged PS colloids were synthesized via polymerization of styrene by using a cationic initiator. In the subsequent coating process, silica formed shell on the surfaces of core PS particles via the ammonia-catalyzed hydrolysis and condensation of tetraethoxysilane. Neither centrifugation/water wash/redispersion cycle process nor surface modification or addition surfactant was needed in the whole process. The morphology of the abrasives was characterized by scanning electron microscope. Transmission electron microscope and energy dispersive X-ray analysis results indicated that silica layer was successfully coated onto the surfaces of PS particles. Composite abrasive has a core-shell structure and smooth surface. The chemical mechanical polishing performances of the composite abrasive and conventional colloidal silica abrasive on blanket copper wafers were investigated. The root mean square roughness decreases from 4.27 nm to 0.56 nm using composite abrasive. The PS/SiO2 core-shell composite abrasives exhibited little higher material removal rate than silica abrasives.

  2. A highly porous NiO/polyaniline composite film prepared by combining chemical bath deposition and electro-polymerization and its electrochromic performance

    Science.gov (United States)

    Xia, X. H.; Tu, J. P.; Zhang, J.; Wang, X. L.; Zhang, W. K.; Huang, H.

    2008-11-01

    A highly porous NiO/polyaniline (PANI) composite film was prepared on ITO glass by combining the chemical bath deposition and electro-polymerization methods, successively. The porous NiO film acts as a template for the preferential growth of PANI along NiO flakes, and the NiO/PANI composite film has an intercrossing net-like morphology. The electrochromic performance of the NiO/PANI composite film was investigated in 1 M LiClO4+1 mM HClO4/propylene carbonate (PC) by means of transmittance, cyclic voltammetry (CV) and chronoamperometry (CA) measurements. The NiO/PANI thin film exhibits a noticeable electrochromism with reversible color changes from transparent yellow to purple and presents quite good transmittance modulation with a variation of transmittance up to 56% at 550 nm. The porous NiO/polyaniline (PANI) composite film also shows good reaction kinetics with fast switching speed, and the response time for oxidation and reduction is 90 and 110 ms, respectively.

  3. A highly porous NiO/polyaniline composite film prepared by combining chemical bath deposition and electro-polymerization and its electrochromic performance

    International Nuclear Information System (INIS)

    A highly porous NiO/polyaniline (PANI) composite film was prepared on ITO glass by combining the chemical bath deposition and electro-polymerization methods, successively. The porous NiO film acts as a template for the preferential growth of PANI along NiO flakes, and the NiO/PANI composite film has an intercrossing net-like morphology. The electrochromic performance of the NiO/PANI composite film was investigated in 1 M LiClO4+1 mM HClO4/propylene carbonate (PC) by means of transmittance, cyclic voltammetry (CV) and chronoamperometry (CA) measurements. The NiO/PANI thin film exhibits a noticeable electrochromism with reversible color changes from transparent yellow to purple and presents quite good transmittance modulation with a variation of transmittance up to 56% at 550 nm. The porous NiO/polyaniline (PANI) composite film also shows good reaction kinetics with fast switching speed, and the response time for oxidation and reduction is 90 and 110 ms, respectively.

  4. ZnO nanorod arrays prepared by chemical bath deposition combined with rapid thermal annealing: structural, photoluminescence and field emission characteristics

    International Nuclear Information System (INIS)

    ZnO nanorod arrays were prepared by low temperature chemical bath deposition (CBD) combined with rapid thermal annealing (RTA) under different ambient conditions. The structure and morphology of the synthesized ZnO have been characterized by field-emission scanning electron microscopy (FESEM) and x-ray diffraction (XRD). The obtained ZnO samples are highly crystalline with a hexagonal wurtzite phase and also display well-aligned array structure. A pronounced effect on increased nanorod length was found for the RTA-treated ZnO as compared to the as-grown ZnO. Analysis of XRD indicates that the (0 0 2) feature peak of the as-grown ZnO was shifted towards a lower angle as compared to the peaks of RTA-treated ZnO samples due to the reduction of tensile strain along the c-axis by RTA. Photoluminescence (PL) studies reveal that the ZnO nanorod arrays receiving RTA in an O2 environment have the sharpest UV emission band and greatest intensity ratio of near band-edge emission (NBE) to deep level emission (DLE). Additionally, the effects of RTA on the field emission properties were evaluated. The results demonstrate that RTA an O2 environment can lower the turn-on field and improve the field enhancement factor. The stability of the field emission current was also tested for 4 h. (paper)

  5. Ordered silicon nanowire arrays prepared by an improved nanospheres self-assembly in combination with Ag-assisted wet chemical etching

    Science.gov (United States)

    Jia, Guobin; Westphalen, Jasper; Drexler, Jan; Plentz, Jonathan; Dellith, Jan; Dellith, Andrea; Andrä, Gudrun; Falk, Fritz

    2016-04-01

    An improved Langmuir-Blodgett self-assembly process combined with Ag-assisted wet chemical etching for the preparation of ordered silicon nanowire arrays is presented in this paper. The new process is independent of the surface conditions (hydrophilic or hydrophobic) of the substrate, allowing for depositing a monolayer of closely packed polystyrene nanospheres onto any flat surface. A full control of the morphology of the silicon nanowire is achieved. Furthermore, it is observed that the formation of porous-Si at the tips of the nanowires is closely related to the release of Ag nanoparticles from the Ag mask during the etching, which subsequently redeposit on the surface initially free of Ag, and these Ag nanoparticles catalyze the etching of the tips and lead to the porous-Si formation. This finding will help to improve the resulting nano- and microstructures to get them free of pores, and renders it a promising technology for low-cost high throughput fabrication of specific optical devices, photonic crystals, sensors, MEMS, and NEMS by substituting the costly BOSCH process. It is shown that ordered nanowire arrays free of porous structures can be produced if all sources of Ag nanoparticles are excluded, and structures with aspect ratio more than 100 can be produced.

  6. Step Coverage and Electrical Properties of (Ba, Sr)TiO3 Films Prepared by Liquid Source Chemical Vapor Deposition Using TiO(DPM)2

    Science.gov (United States)

    Kawahara, Takaaki; Yamamuka, Mikio; Makita, Tetsuro; Naka, Jiro; Yuuki, Akimasa; Mikami, Noboru; Ono, Kouichi

    1994-09-01

    Thin films of (Ba, Sr)TiO3 (BST) with high dielectric constant were prepared on Pt/ SiO2/Si substrates of 6-inch-diameter by liquid source chemical vapor deposition using Ba(DPM)2, Sr(DPM)2 and TiO(DPM)2 (DPM=dipivaloylmethanato; C11H19O2) dissolved in tetrahydrofuran (THF). The reproducibility of ±3 % for the film composition was achieved by optimizing the deposition procedures. It was found that the coverage of 72%, obtained at the substrate temperature T s=753 K, was better than those obtained using other Ti sources such as Ti(O-i-Pr)4 (TTIP) and Ti(O-i-Pr)2(DPM)2. The electrical properties of the 480-Å-thick BST film, deposited at T s=753 K using TiO(DPM)2, were as follows: dielectric constant ɛ=230, equivalent SiO2 thickness t eq=7.8 Å, leakage current density J L=6.7×10-6 A/cm2 at 1.65 V and dielectric loss tan δ=0.013.

  7. The preparation and properties of Y2O3/AlN anti-reflection films on chemical vapor deposition diamond

    International Nuclear Information System (INIS)

    Yttrium oxide (Y2O3) films have successfully been applied as anti-reflection (AR) and anti-oxidation films for diamond. For significant adhesion improvement between Y2O3 coating and diamond, aluminum nitride (AlN) as an interlayer is introduced. Y2O3 and AlN films were prepared by RF magnetron sputtering of Y2O3 ceramic target in Ar atmosphere and pure Al metal target in Ar + N2 atmosphere, respectively. The Y2O3 and AlN films were studied by X-ray diffraction, X-ray photoelectron spectroscopy, Atomic force microscopy and Spectroscopic ellipsometry. Adherent Y2O3/AlN films on high optical quality chemical vapor deposition diamond with optimum thicknesses for infrared transmission enhancement in 8–10 μm were obtained by a Fourier transform infrared spectrometer. More than 28% increase in maximum transmission was observed for Y2O3/AlN//Diamond//AlN/Y2O3. Comparing between the designed and experimental AR effects for Y2O3/AlN film in 8–10 μm wavebands, experimental average AR effects are smaller for the absorption and scattering loss. AR effects for the Y2O3/AlN films on CVD diamond are proved to be excellent.

  8. Preparation and textural characterisation of activated carbon from vine shoots ( Vitis vinifera) by H 3PO 4—Chemical activation

    Science.gov (United States)

    Corcho-Corral, B.; Olivares-Marín, M.; Fernández-González, C.; Gómez-Serrano, V.; Macías-García, A.

    2006-06-01

    An abundant and low-cost agricultural waste as vine shoots ( Vitis vinifera) (VS), which is generated by the annual pruning of vineyards, has been used as raw material in the preparation of powder activated carbon (AC) by the method of chemical activation with phosphoric acid. After size reduction, VS were impregnated for 2 h with 60 wt.% H 3PO 4 solution at room temperature, 50 and 85 °C. The three impregnated products were carbonised at 400 °C. The product impregnated at 50 °C was heated either first at 150-250 °C and then at 400 °C or simply at 350-550 °C in N 2 atmosphere. The time of isothermal treatment after each dynamic heating was 2 h. The carbons were texturally characterised by gas adsorption (N 2, -196 °C), mercury porosimetry, and density measurements. FT-IR spectroscopy was also applied. Better developments of surface area and microporosity are obtained when the impregnation of VS with the H 3PO 4 solution is effected at 50 °C and for the products heated isothermally at 200 and 450 °C. The mesopore volume is also usually higher for the products impregnated and heated at intermediate temperatures.

  9. Solution preparation

    International Nuclear Information System (INIS)

    Reviewed in this statement are methods of preparing solutions to be used in laboratory experiments to examine technical issues related to the safe disposal of nuclear waste from power generation. Each approach currently used to prepare solutions has advantages and any one approach may be preferred over the others in particular situations, depending upon the goals of the experimental program. These advantages are highlighted herein for three approaches to solution preparation that are currently used most in studies of nuclear waste disposal. Discussion of the disadvantages of each approach is presented to help a user select a preparation method for his particular studies. Also presented in this statement are general observations regarding solution preparation. These observations are used as examples of the types of concerns that need to be addressed regarding solution preparation. As shown by these examples, prior to experimentation or chemical analyses, laboratory techniques based on scientific knowledge of solutions can be applied to solutions, often resulting in great improvement in the usefulness of results

  10. Determination of chemical oxygen demand in heterogeneous solid or semisolid samples using a novel method combining solid dilutions as a preparation step followed by optimized closed reflux and colorimetric measurement

    OpenAIRE

    Noguerol Arias, Joan; Rodríguez-Abalde, Ángela; Romero, Eva; Flotats Ripoll, Xavier

    2012-01-01

    This paper reports the development of an innovative sample preparation method for the determination of the chemical oxygen demand (COD) in heterogeneous solid or semisolid samples, with high suspended solids and COD concentrations, using an optimized closed re flux colorimetric method.

  11. Ultra-high performance liquid chromatography coupled with quadrupole/time of flight mass spectrometry based chemical profiling approach for the holistic quality control of complex Kang-Jing formula preparations.

    Science.gov (United States)

    Yang, Xiao-Huan; Cheng, Xiao-Lan; Qin, Bing; Cai, Zhuo-Ya; Cai, Xiong; Liu, Shao; Wang, Qi; Qin, Yong

    2016-05-30

    The Kang-Jing (KJ) formula is a compound preparation made from 12 kinds of herbs. So far, four different methods (M1-M4) have been documented for KJ preparation, but the influence of preparation methods on the holistic quality of KJ have remained unknown. In this study, a strategy was proposed to investigate the influence of different preparation methods on the holistic quality of KJ using ultra-high performance liquid chromatography coupled with quadrupole/time of flight mass spectrometry (UHPLC-QTOF-MS/MS) based chemical profiling. A total of 101 compounds mainly belonging to flavonoids, tanshinones, monoterpene glycosides, triterpenoid saponins, alkaloids, phenolic acids and volatile oils, were identified. Among these compounds, glaucine was detected only in M3/M4 samples, while two dehydrocorydaline isomers merely detected in M2/M3/M4 samples. Tetrahydrocolumbamine, ethylic lithospermic acid, salvianolic acid E and rosmarimic acid were only detected in M1/M3/M4 samples. In the subsequent quantitative analysis, 12 major compounds were determined by UHPLC-MS/MS. The proposed method was validated with respect to linearity, accuracy, precision and recovery. It was found that the contents of marker compounds varied significantly in samples prepared by different methods. These results demonstrated that preparation method does significantly affect the holistic quality of KJ. UHPLC-QTOF-MS/MS based chemical profiling approach is efficient and reliable for comprehensive quality evaluation of KJ. Collectively, this study provide the chemical evidence for revealing the material basis of KJ, and establish a simple and accurate chemical profiling method for its quality control. PMID:26977585

  12. Sol-gel process preparation and evaluation of the analytical performances of an hydrazine specific chemical sensor; Preparation par procede sol-gel et evaluation des performances analytiques d`un capteur chimique specifique de l`hydrazine

    Energy Technology Data Exchange (ETDEWEB)

    Gojon, C

    1996-12-01

    The realisation of optical fibers active chemical collector to analyze hydrazine in line, in the spent fuel reprocessing process is the subject of this work. The p.dimethyl-amino-benzaldehyde has been chosen as reagent for its chemical and optical properties. 186 refs.

  13. Co3O4 protective coatings prepared by Pulsed Injection Metal Organic Chemical Vapour Deposition

    DEFF Research Database (Denmark)

    Burriel, M.; Garcia, G.; Santiso, J.;

    2005-01-01

    deposition temperature. Pure Co3O4 spinel structure was found for deposition temperatures ranging from 360 to 540 degreesC. The optimum experimental parameters to prepare dense layers with a high growth rate were determined and used to prepare corrosion protective coatings for Fe-22Cr metallic interconnects...

  14. Possibilities of biodieses prepared from used vegetable oils by their physico-chemical properties; Perpectivas de los biodiesel preparados a partir de aceites vegetales usados, en base a sus propiedades fisicoquimicas

    Energy Technology Data Exchange (ETDEWEB)

    Poblet Carrilo de Albornoz, F.

    1998-12-31

    In this work are presented the possibilities that bio diesel that are prepared from used vegetable oils as fuel for Diesel engines, and the value added of these waste as sources of renewable power, for domestic and industrial sector. The most characteristics chemical-physical properties of these products mentioned in specifications no officially approved, are compared with the same properties of diesel oil, and respect with another more popular bio diesel. (Author) 3 refs.

  15. Chemical characterization by GC-MS and in vitro activity against Candida albicans of volatile fractions prepared from Artemisia dracunculus, Artemisia abrotanum, Artemisia absinthium and Artemisia vulgaris

    OpenAIRE

    Obistioiu, Diana; Romeo T. Cristina; Schmerold, Ivo; Chizzola, Remigius; Stolze, Klaus; Nichita, Ileana; Chiurciu, Viorica

    2014-01-01

    Background A large number of essential oils is reported to have significant activity against Candida albicans. But the different chemical composition influences the degree of their activity. The intention of this study was to investigate the chemical composition and the activity against Candida albicans of volatile oils obtained from Artemisia dracunculus, A. abrotanum, A. absinthium and A. vulgaris (Asteraceae). The aim of the study was to identify new chemical compounds that have effect aga...

  16. A polymer composite consists of electrochemical reduced graphene oxide/polyimide/chemical reduced graphene oxide for effective preparation of SnSe by electrochemical atomic layer deposition method with enhanced electrochemical performance and surface area

    International Nuclear Information System (INIS)

    A novel polymer electrode is prepared by incorporating polyimide (PI) with chemical reduced graphene oxide (rGO). Then modified this PI/RGO electrode with a layer of electrochemical-reduced graphene oxide (EGO), and by this way the expected EGO/PI/RGO electrode is obtained. Compared with bare PI/RGO film, the hybrid EGO/PI/RGO electrode own large active area and excellent conductivity, which offers more extensive field to prepare compound and more sensitive surface to detect electrochemical signal. SnSe is prepared on this modified substrate by electrochemical atomic layer deposition (EC-ALD) technology. Moreover, SnSe deposit on bare PI/RGO electrode by EC-ALD method is also done for comparison. Open-circuit potential (OCP) and Mott–Schottky measurement indicated the obtained SnSe is a p-type semiconductor. Moreover, the semiconductor appears more excellent photoelectric property on modified electrode

  17. 具有高比表面积的稻壳灰的制备及其化学活性的研究%Study on Preparation of Rice Husk Ash with High Specific Surface Area and Its Chemical Reactivity

    Institute of Scientific and Technical Information of China (English)

    冯庆革; 林清宇; 童张法; S.Sugita

    2004-01-01

    Preparation of rice husk ash with high specific surface area and chemical reactivity of the product are reported in this paper. The amorphous rice husk ash with high specific surface area of 311 m2·g-1 was produced by heating acid treated rice husk at 700℃ for 4 h. The isotherms of rice husk ash are similar in shape to type Ⅱof Brunaner's classification with mesopores being predominant. The rice husk ash has a high chemical reactivity,especially that pretreated with acid. This chemical reactivity depends on ashing temperature and pretreatment conditions. There is an exponential relation between the specific surface area of rice husk ash and the change in the conductivity of saturated Ca(OH)2 solution with rice husk ash, from which the specific surface area can be known according to the conductivity change.

  18. Preparation of an antitumor and antivirus agent: chemical modification of α-MMC and MAP30 from Momordica Charantia L. with covalent conjugation of polyethyelene glycol

    Directory of Open Access Journals (Sweden)

    Meng Y

    2012-06-01

    Full Text Available Yao Meng,1,2 Shuangfeng Liu,1 Juan Li,3 Yanfa Meng,3 Xiaojun Zhao2,41School of Medical Laboratory Science, Chengdu Medical College, Chengdu, China; 2West China Hospital Laboratory of Nanomedicine and Institute for Nanobiomedical Technology and Membrane Biology, Sichuan University, Chengdu, China; 3Key Laboratory of Bio-resources and Eco-environment Ministry of Education/Animal Disease Prevention and Food Safety Key Laboratory of Sichuan Province, College of Life Science, Sichuan University, Chengdu, China; 4Center for Biomedical Engineering, Massachusetts Institute of Technology, Cambridge, MA, USABackground: Alpha-momorcharin (α-MMC and momordica anti-HIV protein (MAP30 derived from Momordica charantia L. have been confirmed to possess antitumor and antivirus activities due to their RNA-N-glycosidase activity. However, strong immunogenicity and short plasma half-life limit their clinical application. To solve this problem, the two proteins were modified with (mPEG2-Lys-NHS (20 kDa.Methodology/principal findings: In this article, a novel purification strategy for the two main type I ribosome-inactivating proteins (RIPs, α-MMC and MAP30, was successfully developed for laboratory-scale preparation. Using this dramatic method, 200 mg of α-MMC and about 120 mg of MAP30 was obtained in only one purification process from 200 g of Momordica charantia seeds. The homogeneity and some other properties of the two proteins were assessed by gradient SDS-PAGE, electrospray ionization quadruple mass spectrometry, and N-terminal sequence analysis as well as Western blot. Two polyethylene glycol (PEGylated proteins were synthesized and purified. Homogeneous mono-, di-, or tri-PEGylated proteins were characterized by matrix-assisted laser desorption ionization-time of flight mass spectrometry. The analysis of antitumor and antivirus activities indicated that the serial PEGylated RIPs preserved moderate activities on JAR choriocarcinoma cells and herpes simplex

  19. 99mTc bone scanning agents preparation and chemical analysis of Tc(Sn)pyrophosphate, Tc(Sn)MDP and Tc(Sn)HMDP

    International Nuclear Information System (INIS)

    This thesis describes a comparison of the preparation, composition and properties of three bone scanning agents: 99mTc(Sn)pyrophosphate, 99mTc(Sn)MDP and 99mTc(Sn)HMDP. This study has been performed for two reasons: First to investigate the preparation and composition of the radiopharmaceuticals as a function of experimental conditions. Together with previously reported results for 99mTc(Sn)EHDP, obtained in a similar way, this enables to use well-defined preparations of the bone scanning agents. Secondly to gain an insight in the mechanism in which the agents behave 'in vivo'. Because the 'in vivo' process is too complicated to study directly, it seemed more appropriate to perform 'in vitro' investigations as simplifications of the 'in vivo' situation. 304 refs.; 26 figs.; 31 tabs

  20. The study on the preparation and chemical states of SIMFUELs, (Eu, U)O2+x and (Mo, Ru, Pd) alloys

    International Nuclear Information System (INIS)

    Some works were performed to examine the behavior of some fission products which are known to be soluble as oxides and insoluble as alloys in UO2 fuel matrix. For the purpose, the SIMFUELs, (Eu, U)O2+x were prepared in the reducing condition that was in a stream of pure H2 and for 4 hours at 1700 deg C. And insoluble metallic alloys composed of Mo-Ru-Pd were synthesized by the Argon arc melting method. The composition and some physicochemical properties of prepared SIMFUELs and alloys were measured by EPMA, SEM and XPS. (author). 6 refs., 2 tabs., 4 figs

  1. WO3-TiO2 monolithic catalysts for high temperature SCR of NO by NH3. Influence of preparation method on structural and physico-chemical properties, activity and durability

    International Nuclear Information System (INIS)

    The WO3-TiO2 catalysts with different WO3 loadings prepared by the coprecipitation method were investigated in comparison with those prepared by the conventional impregnation method for the activity and durability in the high temperature SCR of NO by NH3 and the structural and physico-chemical properties which were characterized by BET and XRD measurements, IR, Raman and XPS spectroscopies. The catalyst prepared by coprecipitation, as compared with that prepared by impregnation, was found to exhibit a higher SCR activity at high temperatures and also to possess a larger surface area, higher Broensted acidity and larger monolayer capacity of the support with WO3. Increasing the WO3 loading of the catalysts enhances the SCR activity and simultaneously increases the Broensted acidity. The observed improvement of SCR activity for the catalyst prepared by coprecipitation is mainly attributed to the higher Broensted acidity and the presence of the more highly dispersed WO3 species which is suggested by the larger monolayer capacity of ca. 13 μmol(W)/m2 and no crystalline WO3 on TiO2 detected with XRD at the high WO3 loading up to 40 wt.%. The catalyst with 20 wt.% WO3, as compared with that prepared by impregnation, was found to exhibit a better thermal durability at high temperatures from 550 to 600 C. The better durability is attributed to that the reduction of the surface area and the formation and subsequent growth of crystalline WO3 upon aging are more remarkably inhibited. (author)

  2. Development of Chemical Fingerprints for Quality Control of Xiong Ma Tang and its Related Preparations by High-Performance Liquid Chromatography.

    Science.gov (United States)

    Liu, Hengyan; Guo, Jiansheng; Li, Zhi; Zhang, Xiaodan; Liu, Xiangqian; Yook, Changsoo

    2016-02-01

    Xiong Ma Tang (XMT), one of the ancient herbal prescriptions, has been used in treatment of migraine disease. In this study, efficient high-performance liquid chromatographic fingerprints were developed for identification of 11 major marker components, named 1-(β-D-ribofuranosyl)-1H-1,2,4-triazone, gastrodin, ligustrazine, 3,4-bihydroxy benzaldehyde, p-hydroxy benzaldehyde, p-hydroxybenzoic acid, benzoic acid, vanillin, ferulic acid, caffeic acid and senkyunolide I, respectively, in XMT and three related preparations. The analysis of 11 marker compounds was carried out using a Kromasil C18 reserved-phase column (5 μm, 4.6 × 250 mm) and gradient elution with methanol and aqueous phosphoric acid (0.1%, v/v). The flow rate was 1.0 mL/min and the detector wavelength was set at 276 nm. Mean chromatograms and correlation coefficients of samples were calculated by the software "Similarity Evaluation System for Chromatographic Fingerprint of Traditional Chinese Medicine". The correlation coefficients of XMT and three related preparations ranged from 0.935 to 0.986, 0.909 to 0.949, 0.900 to 0.926 and 0.937 to 0.988, respectively. It was the first time 11 peaks of XMT and three related preparations were identified by comparing with standard compounds. These results have shown that the developed method was efficient for the quality evaluation of XMT and its related preparations. PMID:26472809

  3. Physical and tribological properties of a-Si1-xCx:H coatings prepared by r.f. plama-assisted chemical vapour deposition

    International Nuclear Information System (INIS)

    A-Si1-xCx:H films deposited by r.f. plasma-assisted chemical vapour deposition were studied as a function of their composition. The friction and wear properties were investigated with the help of a conventional ball-on-disc apparatus. These results are correlated with chemical (Si/C atomic ratio) and structural (Raman and infrared spectroscopy) properties. The friction coefficient in a humid ambient atmosphere changes markedly with the carbon fraction and reaches a value as low as 0.05 for coatings with 70 to 90 at.% C. The carbon-rich films consist of diamond-like carbon with silicon. (orig.)

  4. Analysis on chemical components changes in preparation process of cellulosic ethanol from poplar wood%杨木制备纤维乙醇过程中化学成分变化的分析

    Institute of Scientific and Technical Information of China (English)

    闫兴伟; 崔琳; 张林; 王芳; 陈茜文

    2015-01-01

    杨树是我国重要的速生树种。以杨木为原料制备生物乙醇是解决当今能源问题的一项新的尝试。对杨木原料蒸汽爆破预处理后以及菌处理后的化学成分及化学性质进行了测定分析。通过对比其化学成分(纤维素、木素、半纤维素、抽出物、灰分及蛋白质)的变化,研究了以杨木为原料制备生物乙醇生产过程中化学成分变化机理,旨在为指导杨木制备木质纤维乙醇的生产,并为发酵后副产物的回收再利用提供理论依据。%Poplar is an important fast-growing species in China. The preparation of bio-ethanol with poplar wood as the raw material is a new attempt to solve today’s energy problems. After steam-exploded pretreatment and then bacteria treatment to the poplar wood raw materials, the materials’ chemical composition and properties were measured and analyzed. Through contrasting the changes of the materials’ chemical composition(cellulose, lignin, hemicelluloses, extracts, ash and protein), the mechanism of chemical change of the tested materials in the bioethanol production process prepared from poplar wood was studied, the surplus product contained 64.07%lignin, 6.78% cellulose and 6.88% hemicellulose. The results provide a theoretical basis for guiding the preparation of poplar wood cellulosic ethanol production, and the subsequent recycling of fermentation by-products.

  5. Chemical and Environmental Technology.

    Science.gov (United States)

    Sheather, Harry

    The two-year curriculum in chemical technology presented in the document is designed to prepare high school graduates for technical positions in the chemical industry. Course outlines are given for general chemistry, chemical calculations, quantitative analysis, environmental chemistry, organic chemistry 1 and 2, instrumental analysis, and…

  6. Texture control and ferroelectric properties of Pb(Nb,Zr,Sn,Ti)O3 thin films prepared by chemical solution method

    International Nuclear Information System (INIS)

    A chelating and spin-coating procedure was used to prepare antiferroelectric thin films of Pb0.99Nb0.02[(Zr0.84Sn0.16)0.982Ti0.018]0.98O3.By controlling substrate and thermal processing conditions, films with strong (100) and (111) textures, as well as without textures, were prepared. These antiferroelectric films showed the characteristic double hysteresis polarization vs. electric field loops. An orientation dependence of the critical field for the antiferroelectric-to-ferroelectric phase transition was also observed. In addition, when the applied voltage exceeded a critical level during the first 'ramp up,' an abnormal reduction in the area of the hysteresis loop was noticed in the (100) and (111) textured films.

  7. Structural and XPS studies of PSi/TiO{sub 2} nanocomposites prepared by ALD and Ag-assisted chemical etching

    Energy Technology Data Exchange (ETDEWEB)

    Iatsunskyi, Igor, E-mail: yatsunskiy@gmail.com [NanoBioMedical Centre, Adam Mickiewicz University, 85 Umultowska Str., 61-614 Poznan (Poland); Kempiński, Mateusz [NanoBioMedical Centre, Adam Mickiewicz University, 85 Umultowska Str., 61-614 Poznan (Poland); Faculty of Physics, Adam Mickiewicz University, Umultowska 85, 61-614 (Poland); Nowaczyk, Grzegorz; Jancelewicz, Mariusz [NanoBioMedical Centre, Adam Mickiewicz University, 85 Umultowska Str., 61-614 Poznan (Poland); Pavlenko, Mykola [Department of Experimental Physics, Odessa National I.I. Mechnikov University, 42, Pastera Str., 65023 Odessa (Ukraine); Załęski, Karol [NanoBioMedical Centre, Adam Mickiewicz University, 85 Umultowska Str., 61-614 Poznan (Poland); Jurga, Stefan [NanoBioMedical Centre, Adam Mickiewicz University, 85 Umultowska Str., 61-614 Poznan (Poland); Department of Macromolecular Physics, Adam Mickiewicz University, Umultowska 85, 61-614 Poznan (Poland)

    2015-08-30

    Highlights: • Porous silicon/TiO{sub 2} nanocomposites have been investigated. • Morphology and chemical composition of PSi/TiO{sub 2} nanocomposites were established. • Valence-band XPS maximums for PSi/TiO{sub 2} nanocomposites were found and analyzed. - Abstract: PSi/TiO{sub 2} nanocomposites fabricated by atomic layer deposition (ALD) and metal-assisted chemical etching (MACE) were investigated. The morphology and phase structure of PSi/TiO{sub 2} nanocomposites were studied by means of scanning electron microscopy (SEM), transmission electron microscopy (TEM) with an energy dispersive X-ray spectroscopy (EDX) and Raman spectroscopy. The mean size of TiO{sub 2} nanocrystals was determined by TEM and Raman spectroscopy. X-ray photoelectron spectroscopy (XPS) was used to analyze the chemical elemental composition by observing the behavior of the Ti 2p, O 1s and Si 2p lines. TEM, Raman spectroscopy and XPS binding energy analysis confirmed the formation of TiO{sub 2} anatase phase inside the PSi matrix. The XPS valence band analysis was performed in order to investigate the modification of PSi/TiO{sub 2} nanocomposites electronic structure. Surface defects states of Ti{sup 3+} at PSi/TiO{sub 2} nanocomposites were identified by analyzing of XPS valence band spectra.

  8. Preparation of Iron-Nitride Magnetic Fluid by Vapor-Liquid Chemical Reaction%气-液化学反应制备氮化铁磁性液体

    Institute of Scientific and Technical Information of China (English)

    郭广生; 王志华; 余实; 杨福明

    2000-01-01

    通过氨气和五羰基铁之间的气-液化学反应,制备出了稳定的氮化铁磁性液体. 较为详细地研究了原料的配比、反应温度、表面活性剂的种类及用量等实验参数对产品性能的影响. 利用XRD、TEM和振动样品磁强计(VSM)等技术对产品?的化学组成、固体粒子的粒径、晶型及磁性能进行了测定. 制备的磁性液体具有较高的饱和磁化强度,达到0.134T.%This paper introduced the preparation of stable iron-nitride magnetic fluid by vapor-liquid chemical reaction between iron carbonyl and ammonia. The effects of experiment parameters, such as reactant proportion, reaction temperature, the type and the dosage of the surfactant on product properties were studied in detail. X-ray diffraction(XRD), transmission electron microscope(TEM) and vibrating-sample magnetometer(VSM) were carried out to measure the chemical structure, the crystal style and the magnetic property. The prepared magnetic fluids have high performances with respect to saturation magnetization, up to 0.134T.

  9. Electrical properties and enhanced room temperature magnetoresistance in La0.7Ca0.2Sr0.1MnO3/Pd composites prepared by chemical plating

    International Nuclear Information System (INIS)

    A series of bulk polycrystalline La0.7Ca0.2Sr0.1MnO3 (LCSMO)/Pd composites were prepared by chemical plating and structural, electrical, magnetic, and magnetoresistance (MR) properties were investigated. It is found that Pd additions are uniformly distributed on the grain boundaries of the LCSMO grains, which decrease the resistivity and the saturation magnetic moment of the matrix. An interesting phenomenon is observed that at a given field, when the plating time increases, the MR increases at low addition level (0>t (plating time)40 min), indicating an optimal plating time of 40 min, at which the MR value is maximum. Our analysis suggests that the improvement of grain boundaries originating from Pd addition plays an important role in enhancing the MR. - Highlights: ► The La0.7Ca0.2Sr0.1MnO3/Pd composites were prepared successfully by chemical plating. ► Pd additions were uniformly distributed on the grain boundaries of the LCSMO grains. ► The value of MR exhibited dramatically with increase of plating time. ► When the plating time is 40 min, the MR value reaches the maximum value.

  10. Enhanced Photoluminescence and Raman Properties of Al-Doped ZnO Nanostructures Prepared Using Thermal Chemical Vapor Deposition of Methanol Assisted with Heated Brass

    OpenAIRE

    Thandavan, Tamil Many K.; Gani, Siti Meriam Abdul; San Wong, Chiow; Md. Nor, Roslan

    2015-01-01

    Vapor phase transport (VPT) assisted by mixture of methanol and acetone via thermal evaporation of brass (CuZn) was used to prepare un-doped and Al-doped zinc oxide (ZnO) nanostructures (NSs). The structure and morphology were characterized by field emission scanning electron microscopy (FESEM) and x-ray diffraction (XRD). Photoluminescence (PL) properties of un-doped and Al-doped ZnO showed significant changes in the optical properties providing evidence for several types of defects such as ...

  11. NiO/Al2O3 oxygen carriers for chemical-looping combustion prepared by impregnation and deposition-precipitation methods

    OpenAIRE

    Gayán Sanz, Pilar; Dueso, Cristina; Abad Secades, Alberto; Adánez Elorza, Juan; Diego Poza, Luis F. de; García Labiano, Francisco

    2009-01-01

    Ni-based oxygen carriers (OC) with different NiO content were prepared by incipient wet impregnation, at ambient (AI), and hot conditions (HI) and by deposition-precipitation (DP) methods using -Al2O3 and -Al2O3 as supports. The OC were characterized by BET, Hg porosimetry, mechanical strength, TPR, XRD and SEM/EDX techniques. Reactivity of the OC was measured in a termogravimetric analyzer and methane combustion selectivity towards CO2 and H2O, attrition rate, and agglomerat...

  12. Chem-prep PZT95/5 for neutron generator applications : the effect of pore former type and density on the depoling behavior of chemically prepared PZT 95/5 ceramics.

    Energy Technology Data Exchange (ETDEWEB)

    Lockwood, Steven John; Scofield, Timothy W.; Yang, Pin; Voigt, James A.; Tuttle, Bruce Andrew; Moore, Roger Howard

    2003-10-01

    The hydrostatically induced ferroelectric(FE)-to-antiferroelectric(AFE) phase transformation for chemically prepared niobium modified PZT 95/5 ceramics was studied as a function of density and pore former type (Lucite or Avicel). Special attention was placed on the effect of different pore formers on the charge release behavior associated with the FE-to-AFE phase transformation. Within the same density range (7.26 g/cm3 to 7.44 g/cm3), results showed that ceramics prepared with Lucite pore former exhibit a higher bulk modulus and a sharper polarization release behavior than those prepared with Avicel. In addition, the average transformation pressure was 10.7% greater and the amount of polarization released was 2.1% higher for ceramics with Lucite pore former. The increased transformation pressure was attributed to the increase of bulk modulus associated with Lucite pore former. Data indicated that a minimum volumetric transformational strain of -0.42% was required to trigger the hydrostatically induced FE-to-AFE phase transformation. This work has important implications for increasing the high temperature charge output for neutron generator power supply units.

  13. Synthesis, characterization and study of magnetic, electrical and dielectric properties of La1−xDyxCo1−yFeyO3 nanoparticles prepared by wet chemical route

    International Nuclear Information System (INIS)

    Dy3+ and Fe3+ co-doped LaCoO3 perovskite nanoparticles were prepared by chemical co-precipitation route. Structural elucidation was carried out by thermo gravimetric analysis (TGA), X-ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier transform infrared (FTIR) spectroscopy. The data of all these characterization techniques confirmed the orthorhombic phase with particles size in the range of 20–60 nm. The magnetic parameters, DC-resistivity and dielectric properties were measured for La1−xDyxCo1−yFeyO3 nanoparticles. The purpose of all these application studies was to evaluate the prepared materials for practical applications. The substitution of Dy3+ and Fe3+ with La3+ and Co3+ respectively greatly influenced the magnetic, DC-resistivity and dielectric parameters. - Highlights: • La1−xDyxCo1−yFeyO3 nanoparticles were prepared in the range 20–60 nm. • 12 Fold increase in DC resistivity achieved for La0.40Dy0.60Co0.40Fe0.60O3. • Paramagnetic to ferromagnetic behavior was observed for La1−xDyxCo1−yFeyO3 nanoparticles

  14. Preparation and characterization of Pd/Al{sub 2}O{sub 3} and Pd nanoparticles as standardized test material for chemical and biochemical studies of traffic related emissions

    Energy Technology Data Exchange (ETDEWEB)

    Leopold, K. [Technische Universitaet Muenchen, Arbeitsgruppe fuer Analytische Chemie, Lichtenbergstrasse 4, D-85747 Garching (Germany)], E-mail: kerstin.leopold@lrz.tum.de; Maier, M.; Schuster, M. [Technische Universitaet Muenchen, Arbeitsgruppe fuer Analytische Chemie, Lichtenbergstrasse 4, D-85747 Garching (Germany)

    2008-05-01

    Palladium model particles similar to those emitted from catalytic car exhaust converters were prepared and characterized with the intention of providing a standardized material for investigations of the chemical behavior and bioavailability of traffic related Pd emissions. Two series of Pd particles were prepared and characterized in detail: Pd nanoparticles (2-4 nm) dispersed on aluminum oxide particles of a diameter range between 0.1 to 30 {mu}m and 'Pd-only' nanoparticles of 5-10 nm in diameter. The Pd/{alpha}-Al{sub 2}O{sub 3} particles are very similar to particles emitted from catalytic converters by mechanical abrasion. The Pd-only particles are useful e.g. for exposure studies in which the presence of aluminum could lead to interferences when studying biological and biochemical effects. The sample preparation procedure of both series was optimized in order to achieve elemental particles with proper sizes and a narrow size distribution. The obtained particles were characterized by transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM), selective area diffraction (SAD), laser granulometry and graphite furnace atomic absorption spectrometry (GFAAS) for the measurement of Pd concentrations.

  15. Physico-Chemical Characterization and Interfacial Electrochemical Properties of Nanoparticles of Anatase-TiO2 Prepared by the Sol-Gel Method

    Directory of Open Access Journals (Sweden)

    Ikram Daou

    2013-07-01

    Full Text Available In this work, we prepared by the sol-gel method titanium dioxide nanoparticles having a large specific area (SBET = 218 m2/g. The isotherm of N2 adsorption-desorption at 77K revealed that it concerns a mesoporous solid with a maximum pore diameter of 43 Å. The X-ray diffraction showed that the solid is constituted of the anatase phase. The transmission electron microscopy revealed us that the synthesized grains of TiO2 are of nanometric sizes (diameter between 8 and 20 nm and manifest under agglomerated shape. The study of its solubility in dispersing phase, by conductometric titrations, showed that the prepared solid is totally insoluble in all the domain of the studied pH. The measured inter-facial electrochemical properties, based on the isotherms of ionic adsorption and the conductometric titrations, are: the point of zero charge found equal to 6,2±0,1, the total number of sites of surface found equal to 5,8 OH/nm2 and the nature of action of the dispersed phase on the dispersing phase which is found organizer of the structure of water. Besides, the difference of the ionizationconstants pK is found superior to 4 for all the adsorbed ions and the constants of surface complexation are independent from the nature of the adsorbed ion.

  16. Multilayer MoS2 prepared by one-time and repeated chemical vapor depositions: anomalous Raman shifts and transistors with high ON/OFF ratio

    Science.gov (United States)

    Wu, Chong-Rong; Chang, Xiang-Rui; Chang, Shu-Wei; Chang, Chung-En; Wu, Chao-Hsin; Lin, Shih-Yen

    2015-11-01

    We show that multilayer molybdenum disulfide (MoS2) grown with the chemical vapor deposition (CVD) may exhibit quite distinct behaviors of Raman shifts from those of exfoliated ones. The anomalous Raman shifts depend on CVD growth modes and are attributed to the modified dielectric screening and interlayer coupling of MoS2 in various growth conditions. With repeated CVD growths, we demonstrated the precise control over the layer number of MoS2. A decently large drain current, high ON/OFF ratio of 105, and enhanced field-effect mobility can be achieved in transistors fabricated on the six-layer MoS2.

  17. Study of the crystallographic phase change on copper (I) selenide thin films prepared through chemical bath deposition by varying the pH of the solution

    Science.gov (United States)

    Sandoval-Paz, M. G.; Rodríguez, C. A.; Porcile-Saavedra, P. F.; Trejo-Cruz, C.

    2016-07-01

    Copper (I) selenide thin films with orthorhombic and cubic structure were deposited on glass substrates by using the chemical bath deposition technique. The effects of the solution pH on the films growth and subsequently the structural, optical and electrical properties of the films were studied. Films with orthorhombic structure were obtained from baths wherein both metal complex and hydroxide coexist; while films with cubic structure were obtained from baths where the metal hydroxide there is no present. The structural modifications are accompanied by changes in bandgap energy, morphology and electrical resistivity of the films.

  18. Low temperature carrier transport study of monolayer MoS2 field effect transistors prepared by chemical vapor deposition under an atmospheric pressure

    International Nuclear Information System (INIS)

    Large size monolayer Molybdenum disulphide (MoS2) was successfully grown by chemical vapor deposition method under an atmospheric pressure. The electrical transport properties of the fabricated back-gate monolayer MoS2 field effect transistors (FETs) were investigated under low temperatures; a peak field effect mobility of 59 cm2V−1s−1 was achieved. With the assist of Raman measurement under low temperature, this work identified the mobility limiting factor for the monolayer MoS2 FETs: homopolar phonon scattering under low temperature and electron-polar optical phonon scattering at room temperature

  19. Low temperature carrier transport study of monolayer MoS{sub 2} field effect transistors prepared by chemical vapor deposition under an atmospheric pressure

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Xinke, E-mail: xkliu@szu.edu.cn, E-mail: wujing026@gmail.com; He, Jiazhu; Tang, Dan; Lu, Youming; Zhu, Deliang; Liu, Wenjun; Cao, Peijiang; Han, Sun [College of Materials Science and Engineering, Shenzhen Engineering Laboratory for Advanced Technology of Ceramics, Nanshan District Key Lab for Biopolymer and Safety Evaluation, Shenzhen University, 3688 Nanhai Ave, Shenzhen 518060 (China); Liu, Qiang; Wen, Jiao; Yu, Wenjie [State Key Laboratory of Functional Materials for Informatics, Shanghai Institute of Microsystem and Information Technology, CAS, 865 Chang Ning Road, Shanghai 200050 (China); Liu, Wenjun [State Key Laboratory of ASIC and System, Department of Microelectronics, Fudan University, 220 Handan Road, Shanghai 200433 (China); Wu, Jing, E-mail: xkliu@szu.edu.cn, E-mail: wujing026@gmail.com [Department of Physics, National University of Singapore, 21 Lower Kent Ridge Road, 117576 Singapore (Singapore); He, Zhubing [Department of Materials Science and Engineering, South University of Science and Technology of China, 1088 Xueyuan Road, Shenzhen 518055 (China); Ang, Kah-Wee [Department of Electrical and Computer Engineering, National University of Singapore, 4 Engineering Drive 3, 117583 Singapore (Singapore)

    2015-09-28

    Large size monolayer Molybdenum disulphide (MoS{sub 2}) was successfully grown by chemical vapor deposition method under an atmospheric pressure. The electrical transport properties of the fabricated back-gate monolayer MoS{sub 2} field effect transistors (FETs) were investigated under low temperatures; a peak field effect mobility of 59 cm{sup 2}V{sup −1}s{sup −1} was achieved. With the assist of Raman measurement under low temperature, this work identified the mobility limiting factor for the monolayer MoS{sub 2} FETs: homopolar phonon scattering under low temperature and electron-polar optical phonon scattering at room temperature.

  20. Physical and Chemical Properties of TiOxNy Prepared by Low-Temperature Oxidation of Ultrathin Metal Nitride Directly Deposited on SiO2

    Institute of Scientific and Technical Information of China (English)

    HAN Yue-Ping; HAN Yan

    2009-01-01

    Physical and chemical properties of titanium oxynitride (TiOxNy) formed by low-temperature oxidation of titanium nitride (TIN) layer are investigated for advanced metal-oxide--semiconductor (MOS) gate dielectric application.TiOx Ny exhibits polycrystalline properties after the standard thermal process for MOS device fabrication,showing the preferred orientation at [200].Superior electrical properties of TiOxNy can be maintained before and after the annealing,probably due to the nitrogen incorporation in the oxide bulk and at the interface.Naturally formed transition layer between TiOxNy and SiO2 is also confirmed.

  1. Dielectric properties and X-ray photoelectron spectroscopic studies of niobium oxide thin films prepared by direct liquid injection chemical vapor deposition method

    International Nuclear Information System (INIS)

    Niobium oxide thin films were grown by direct liquid injection chemical vapor deposition using Nb(OC2H5)5 precursor. Influence of reactant's molar ratios [oxygen:Nb(OC2H5)5] and deposition temperatures on films properties such as growth rate, stoichiometry, crystal structure, morphology, dielectric constant and leakage current were studied. Films start crystallizing above 340 °C in O2 atmosphere and become crystalline at 400 °C. The surface roughness of weakly crystalline and crystalline films was significantly affected by deposition temperatures and reactant's molar ratios. It was found that decrease in surface roughness improved leakage current. X-ray photoelectron spectroscopic studies showed that films were in different oxidation states (Nb2+, Nb4+ and Nb5+). The dielectric constants of films were improved by increasing oxygen ratios. At ratio (150:1), the film showed high dielectric constant value (47) at 340 °C and leakage current density of 2.0 × 10−5 A/cm2 (at 3 V). - Highlights: • High dielectric constant (47) of Nb2O5 thin film with chemical vapor deposition • The change in morphology as a function of growth temperature and O2 molar ratio • A stoichiometric Nb2O5 phase and smooth surface show better electrical properties

  2. Growth and electro-optical properties of Ga-doped ZnO films prepared by aerosol assisted chemical vapour deposition

    International Nuclear Information System (INIS)

    Transparent conductive Ga-doped ZnO thin films were deposited onto glass substrates by a low-cost aerosol assisted chemical vapour deposition technique and the effect of gallium content on the ZnO film growth behaviour and opto-electronic properties was systematically investigated. It is found that, upon increasing Ga addition, the ZnO film crystallinity exhibits a continuous reduction in quality associated with the preferential orientation transformed from (002) to (102). The (002) oriented samples had a microstructure of parallel columnar grains while the (102) oriented coating was thickened by overlapping particles. The ZnO:Ga coatings exhibit high carrier concentration (up to 4.1 × 1020 cm−3) but low carrier mobility (up to 0.8 cm2 V−1 s−1), resulting in a minimum resistivity value of 2.3 × 10−2 Ω cm. The inferior carrier mobility performance could result from a profound ionized and neutral impurity scattering effect. Good visible transmittance (≈ 70–80%) is observed in these ZnO:Ga films and samples with higher carrier density present better infrared reflection performance (up to 37.2% at 2500 nm). - Highlights: • Aerosol assisted chemical vapour deposition of doped zinc oxide thin films • Gallium doping and opto-electronic properties systemically investigated • Growth mechanism changed by % gallium incorporation

  3. Growth and electro-optical properties of Ga-doped ZnO films prepared by aerosol assisted chemical vapour deposition

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Shuqun [School of Engineering and Materials Science, Queen Mary University of London, Mile End Road, London E1 4NS (United Kingdom); Carraro, Giorgio [Department of Chemistry and INSTM, Padova University, Padova 35131 (Italy); Barreca, Davide [CNR-IENI and INSTM, Department of Chemistry, Padova University, Padova 35131 (Italy); Binions, Russell [School of Engineering and Materials Science, Queen Mary University of London, Mile End Road, London E1 4NS (United Kingdom)

    2015-06-01

    Transparent conductive Ga-doped ZnO thin films were deposited onto glass substrates by a low-cost aerosol assisted chemical vapour deposition technique and the effect of gallium content on the ZnO film growth behaviour and opto-electronic properties was systematically investigated. It is found that, upon increasing Ga addition, the ZnO film crystallinity exhibits a continuous reduction in quality associated with the preferential orientation transformed from (002) to (102). The (002) oriented samples had a microstructure of parallel columnar grains while the (102) oriented coating was thickened by overlapping particles. The ZnO:Ga coatings exhibit high carrier concentration (up to 4.1 × 10{sup 20} cm{sup −3}) but low carrier mobility (up to 0.8 cm{sup 2} V{sup −1} s{sup −1}), resulting in a minimum resistivity value of 2.3 × 10{sup −2} Ω cm. The inferior carrier mobility performance could result from a profound ionized and neutral impurity scattering effect. Good visible transmittance (≈ 70–80%) is observed in these ZnO:Ga films and samples with higher carrier density present better infrared reflection performance (up to 37.2% at 2500 nm). - Highlights: • Aerosol assisted chemical vapour deposition of doped zinc oxide thin films • Gallium doping and opto-electronic properties systemically investigated • Growth mechanism changed by % gallium incorporation.

  4. Comparison of two chemical cleavage methods for preparation of a truncated form of recombinant human insulin-like growth factor I from a secreted fusion protein.

    Science.gov (United States)

    Forsberg, G; Baastrup, B; Brobjer, M; Lake, M; Jörnvall, H; Hartmanis, M

    1989-12-01

    We have produced a naturally occurring variant of human insulin-like growth factor I, truncated by three amino acids at the amino terminus. The polypeptide is obtained as a fusion protein in Escherichia coli. The fusion partner is a synthetic IgG-binding peptide. During fermentation the fusion protein is secreted into the medium, and is purified on IgG--Sepharose prior to cleavage. Two different genes for the fusion protein were used, allowing chemical cleavage at either a tryptophan linker or a methionine linker between the fusion partner and the growth factor, using N-chlorosuccinimide (NCS) or cyanogen bromide (CNBr) respectively. A partial CNBr cleavage yielded the native peptide, whereas the NCS cleavage yielded a product in which the single methionine had been oxidized to the sulfoxide. The forms from both cleavage methods exhibited biological activity and were characterized after purification to homogeneity. Both cleavage methods gave products having correct N- and C-terminal ends. The purified product had a biological activity equal to that of corresponding material from natural sources, 15 000 U/mg. Modified forms of truncated IGF-I were also identified, purified and characterized. Modifications such as proteolysis and misincorporation of norleucine for methionine occurred during biosynthesis, while oxidation of methionine took place during both fermentation and chemical cleavage. PMID:2696476

  5. Morphology and chemical state of PVP-protected Pt, Pt–Cu, and Pt–Ag nanoparticles prepared by alkaline polyol method

    International Nuclear Information System (INIS)

    Well-dispersed, uniform monometallic Pt and bimetallic Pt–Cu, and Pt–Ag nanoparticles protected with PVP have been synthesized by a modified-protocol alkaline polyol method. The nanoparticles were characterized by various methods (TEM, XPS, and XRD) to elucidate the relationship between morphology and preparation variables. The average of monodispersed nanoparticles ranged between 4.1 and 4.9 nm. Core–shell structure was obtained in the case of bimetallic nanoparticles. The core of bimetallic nanoparticles was found to be rich in platinum, whereas the shell contained mostly copper or silver. The final structure of bimetallic nanoparticles was found to be determined by the morphology particles resulted in the first reduction step. Explanations are advanced on the light of experimental results.

  6. Effect of annealing temperature on the structural–microstructural and electrical characteristics of thallium bearing HTSC films prepared by chemical spray pyrolysis technique

    Indian Academy of Sciences (India)

    K K Verma; R S Tiwari; O N Srivastava

    2005-04-01

    In order to get good quality reproducible films of Tl : HTSC system, we have studied the different annealing conditions to finally achieve the optimized annealing condition. In the present investigation, Tl–Ca–Ba–Cu–O superconducting films have been prepared on YSZ (100) and MgO (100) single crystal substrates via precursor route followed by thallination. The post deposition heat treatments of the precursor films were carried out for various annealing temperatures (870°C, 890°C) and durations (1 and 2 min). The optimized thallination procedure occurred at 870°C for 2 min into good quality films with c ( = 0) ∼ 103 K for YSZ and c ( = 0) ∼ 98 K for MgO substrates, respectively. Further we have correlated the structural/microstructural characteristics of the films.

  7. Preparation and physico-chemical study of nitroxide radicals. Isotopic marking with carbon 13 and deuterium; Preparations et etudes physico-chimiques de radicaux nitroxydes. Marquage isotopique au carbone 13 et au deuterium

    Energy Technology Data Exchange (ETDEWEB)

    Chapelet-Letourneux, G. [Commissariat a l' Energie Atomique, Grenoble (France). Centre d' Etudes Nucleaires

    1967-07-01

    N-t-butyl-N-phenyl nitroxide is obtained by: a) action of t-butyl-magnesium chloride on nitrobenzene, or of phenyl-magnesium bromide on nitro-t-butane, b) oxidation of N-t-butyl-N-phenylhydroxylamine, c) oxidation of N-t-butylaniline. In these latter two cases, it has been possible to isolate the pure radical and to study it using UV, IR and EPR. It decomposes to give N-t-butylaniline and the N-oxide of N-t-butyl-p-quinon-imine. The action of peracids such as p-nitro-perbenzoic or m-chloro-perbenzoic acids on amines or hydroxylamines leads to the formation of stable or unstable nitroxide radicals easily observable by EPR. Finally, with a view to obtaining definite values for the coupling between the free electron of a nitroxide and carbon 13, the preparation of such radicals marked with {sup 13}C in the {alpha} or {beta} position of the nitroxide function has been carried out. The coupling with an {alpha} carbon 13 is negative and does not appear to vary with the spin density on the nitrogen. The interaction with the p nuclei of the nitrogen depends on the nature of the substituents: the two benzyl protons have a hyperfine splitting a{sub H} which is always less than that of the ethyl. On the other hand, the {sup 13}C coupling is greater in the first case. The usually adopted conformations for the compounds having the carbonyl group cannot account for the observed values of the {beta} couplings. (author) [French] Le N-t-butyl-N-phenyl nitroxyde est obtenu par: a) action du chlorure de t-butylmagnesium sur le nitrobenzene, ou du bromure de phenylmagnesium sur le nitro-t-butane, b) oxydation de la N-t-butyl-N-phenylhydroxylamine, c) oxydation de la N-t-butylaniline. Dans ces deux derniers cas, le radical a pu etre isole pur et etudie par UV, IR et RPE. Il se decompose en N-t-butylaniline et N-oxyde de N-t-butyl-p-quinonimine. L'action de peracides (p-nitroperbenzoique ou m-chloroperbenzoique) sur des amines ou des hydroxylamines conduit a des radicaux nitroxydes

  8. KANJI: AN AYURVEDIC FERMENTATIVE PREPARATION

    OpenAIRE

    Santhosh B; Jadar P. G.; Nageswara Rao

    2012-01-01

    Kanji – A unique Ayurvedic fermentative preparation was prepared as per the textual reference Rasayanasara which is mainly indicated for the Shodhana (purification) of Metals and also for various mercurial processing. But Kanji by this reference is rarely prepared and used. Hence, the pharmaceutical and preliminary physico-chemical findings of this Kanji are reported in this paper. The fermentation process started on 7th day and completed on 31st day. The prepared Kanji was golden brown color...

  9. Strong interfacial magnetic coupling in epitaxial bilayers of LaCoO3/LaMnO3 prepared by chemical solution deposition

    International Nuclear Information System (INIS)

    We report the synthesis of high quality epitaxial bilayers of LaMnO3/LaCoO3 (LCO/LMO) on (001) LaAlO3, by spin-coating of a polymeric aqueous solutions. The bilayer shows a very large increase of the magnetization coercive field (≈ 3000%) with respect to the isolated LMO or LCO films. We suggest that the origin of this effect is a strong Mn4+–O–Co2+ exchange interaction at the interface. Our results demonstrate that a simple chemical method is able to produce high quality epitaxial heterostructures in which interfacial effects can modify substantially the properties of the individual layers. - Highlights: • Synthesis of high quality epitaxial bilayers of LaMnO3/LaCoO3 on (001) LaAlO3 • Polymer assisted deposition method • Interfacial effects can modify substantially the properties of the individual layers

  10. Structure and magnetism of Zn0.9Co0.1O DMS films prepared by chemical solution deposition method

    International Nuclear Information System (INIS)

    The Zn0.9Co0.1O films are fabricated by chemical solution deposition method. All the films have the ZnO wurtzite structure with a preferential orientation along the c-axis. The analysis of X-ray near-edge absorption spectroscopy and X-ray photoelectron spectroscopy indicates that the valence of Co is +2, and there are oxygen vacancies in Zn0.9Co0.1O films annealed in Ar atmosphere. Extended X-ray absorption fine structure results reveal that Co2+ ions have dissolved into ZnO and substituted for Zn2+ ions. Magnetization measurements show that the film annealed in Ar exhibits ferromagnetism which can be explained by the formation of bound magnetic polarons.

  11. Compositional and physico-optical characterization of 0-5% Al-doped zinc oxide films prepared by chemical spray pyrolysis

    Energy Technology Data Exchange (ETDEWEB)

    Romero, R; Lopez-Ibanez, R; Ramos-Barrado, J R; Martin, F; Leinen, D [Laboratorio de Materiales y Superficie (Unidad Asociada al CSIC), Dpto. Fisica Aplicada I and Dpto. IngenierIa Quimica, Universidad de Malaga, E-29071 Malaga (Spain); Dalchiele, E A, E-mail: dietmar@uma.e [Instituto de Fisica, Facultad de IngenierIa, Universidad de la Republica, Herrera y Reissig 565, C.C. 30, 11000 Montevideo (Uruguay)

    2010-03-10

    Highly transparent polycrystalline Al-doped ZnO thin films were deposited in open atmosphere by chemical spray pyrolysis on fused silica and glass substrates at 623 K. The influence of Al doping, 0 to 5%, was studied. XPS results revealed a linear relationship between Al content in the precursor solutions and Al content in the films. XPS depth profiling showed that any carbon contamination is restricted to the uppermost surface of the films. Optical transmission measurements revealed an increasing number of dispersion centres as well as a band gap shift to higher values with increasing Al content in the films. At fixed Al concentration, the comparison of the absorption coefficient for increasing film thickness showed that the films are very homogeneous, not changing their materials properties such as absorption coefficient and band gap.

  12. Influence of double AlN buffer layers on the qualities of GaN films prepared by metal-organic chemical vapour deposition

    Institute of Scientific and Technical Information of China (English)

    Lin Zhi-Yu; Hao Yue; Zhang Jin-Cheng; Zhou Hao; Li Xiao-Gang; Meng Fan-Na; Zhang Lin-Xia; Ai Shan; Xu Sheng-Rui; Zhao Yi

    2012-01-01

    In this paper we report that the GaN thin film is grown by metal-organic chemical vapour deposition on a sapphire (0001) substrate with double AlN buffer layers.The buffer layer consists of a low-temperature (LT) AlN layer and a high-temperature (HT) AlN layer that are grown at 600 ℃ and 1000 ℃,respectively.It is observed that the thickness of the LT-AlN layer drastically influences the quality of GaN thin film,and that the optimized 4.25-min-LT-AlN layer minimizes the dislocation density of GaN thin film.The reason for the improved properties is discussed in this paper.

  13. Low temperature deposition and effect of plasma power on tin oxide thin films prepared by modified plasma enhanced chemical vapor deposition

    International Nuclear Information System (INIS)

    This work presents low temperature (200 and 300 deg. C) thin film deposition of tin oxide (SnO2) using modified plasma enhanced chemical vapor deposition as a function of radio frequency power (100 - 500 W). Stannic chloride (SnCl4) was used as precursor and oxygen (O2, 300 SCCM) as reactant gas. Fine granular morphology was observed with tetragonal rutile structure grown along the [110] direction, at all the deposition conditions. Higher plasma power resulted in smoother morphology, improved crystallinity, and enhanced conductivity. Electrical resistivity value of as low as ∼0.01 Ω cm was obtained at the deposition temperature of 300 deg. C and 250 W of plasma power

  14. Characterization of Pb(Zr, Ti)O sub 3 thin films prepared by metal-organic chemical-vapor deposition using a solid delivery system

    CERN Document Server

    Shin, J C; Hwang, C S; Kim, H J; Lee, J M

    1999-01-01

    Pb(Zr, Ti)O sub 3 (PZT) thin films were deposited on Pt/SiO sub 2 /Si substrates by metal-organic chemical-vapor deposition technique using a solid delivery system to improve the reproducibility of the deposition. The self-regulation mechanism, controlling the Pb-content of the film, was observed to work above a substrate temperature of 620 .deg. C. Even with the self-regulation mechanism, PZT films having low leakage current were obtained only when the molar mixing ratio of the input precursors was 1

  15. Characterization of thin TiO{sub 2} films prepared by plasma enhanced chemical vapour deposition for optical and photocatalytic applications

    Energy Technology Data Exchange (ETDEWEB)

    Sobczyk-Guzenda, A., E-mail: asobczyk@p.lodz.p [Institute of Materials Science and Engineering, Technical University of Lodz, Stefanowskiego 1, 90-924 Lodz (Poland); Gazicki-Lipman, M.; Szymanowski, H.; Kowalski, J. [Institute of Materials Science and Engineering, Technical University of Lodz, Stefanowskiego 1, 90-924 Lodz (Poland); Wojciechowski, P.; Halamus, T. [Department of Molecular Physics, Technical University of Lodz, Stefanowskiego 1, 90-924 Lodz (Poland); Tracz, A. [Centre for Molecular and Macromolecular Studies, Polish Academy of Sciences, Sienkiewicza 112, 90-363 Lodz (Poland)

    2009-07-31

    Thin titanium oxide films were deposited using a radio frequency (RF) plasma enhanced chemical vapour deposition method. Their optical properties and thickness were determined by means of ultraviolet-visible absorption spectrophotometry. Films of the optical parameters very close to those of titanium dioxide have been obtained at the high RF power input. Their optical quality is high enough to allow for their use in a construction of stack interference optical filters. At the same time, these materials exhibit strong photocatalytic effects. The results of structural analysis, carried out by Raman Shift Spectroscopy, show that the coatings posses amorphous structure. However, Raman spectra of the same films subjected to thermal annealing at 450 {sup o}C disclose an appearance of a crystalline form, namely that of anatase. Surface morphology of the films has also been characterized by Atomic Force Microscopy revealing granular, broccoli-like topography of the films.

  16. 甘氨酸亚铁制备及热化学性质研究%Preparation of Ferrous Glycinate and Research on Hot Chemical Properties

    Institute of Scientific and Technical Information of China (English)

    毛玉娥; 雷克林

    2011-01-01

    研究了固相研磨法、固相催化研磨法和熔融法三种实验条件下,甘氨酸与硫酸亚铁铵以物质的量之比2:1反应得到二价亚铁与甘氨酸的配合物.通过对配合物进行红外光谱表征和定量分析,得到二价亚铁配合物的组成为【Fe(Gly)2].最后,根据熔解一量热法的基本操作条件,设计了热化学循环,测量了反应物和产物的标准摩尔溶解焓,结合热化学原理,测定了甘氨酸亚铁的标准摩尔生成焓.%This topic mainly researches the reaction of glycine and ammonium ferrous sulphate at the ratio of the amount of 2:1 to get the complexes of bivalent ferrous and glycine through solid-phase grinding method, solid phase catalysis grinding method and melting method. Through IR characterization and quantitative analysis, we are sure that the composition of ferrous complexes is [Fe(Gly)2]. Finally, according to the basic operation conditions of Dissolve- Quantity hot method, we designed the thermal and chemical circulation, and measured the standards Moore of reactant and product, which is combined with hot dissolving enthalpy chemical principle; we estimate the standard Moore of ferrous glycinate.

  17. Effect of anionic dopants on thickness, morphology and electrical properties of polypyrrole ultra-thin films prepared by in situ chemical polymerization

    International Nuclear Information System (INIS)

    The effect of different dopant anions on deposition and characteristics of polypyrrole (PPy) thin film has been studied in this work. Ultra-thin films of conducting PPy were deposited on insulating surfaces of glass and oxidized silicon wafer by in situ chemical polymerization in the presence of different anionic dopants including sodium dodecylbenzenesulfonate, sodium dodecyl sulfate, α-naphthalene sulfonic acid, anthraquinone-2-sulfonic acid sodium salt monohydrate/5-sulfosalicylic acid dehydrate, and camphor sulfonic acid. Hydrophilic/hydrophobic properties and morphology of the self-assembled monolayer of N-(3-trimethoxysilylpropyl)pyrrole, the surface modifying agent in this work, and PPy thin films were characterized before and after deposition by contact angle measurements, field emission scanning electron microscopy, and atomic force microscopy. Chemical structure, thickness, and conductivity of the thin films were also studied by attenuated total reflectance Fourier transform infrared spectrometer, ellipsometry, and four-point probe measurements. The results showed deposition of thin films of conducting PPy with comparable thickness in the range of 6-31 nm and different morphologies, uniformity, and smoothness with average roughness in the range of 0.3-6 nm and relatively high range of conductivity on the modified surfaces. - Highlights: • Conducting thin films of polypyrrole were deposited on glass and SiO2 substrates. • Surface modification using pyrrole-silane was employed prior to polymerization. • Films as thin as ≈ 7 nm were deposited using different surfactant/counter ions. • Chemistry of the counter ion affects thickness, conductivity and morphology. • Lower thickness/higher conductivity were obtained by structurally flexible dopants

  18. Effect of anionic dopants on thickness, morphology and electrical properties of polypyrrole ultra-thin films prepared by in situ chemical polymerization

    Energy Technology Data Exchange (ETDEWEB)

    Mahmoodian, Mehrnoosh [Dep. of Polymer Engineering, Nanostructured Materials Research Center, Sahand University of Technology, Tabriz 51335-1996 (Iran, Islamic Republic of); Pourabbas, Behzad, E-mail: pourabas@sut.ac.ir [Dep. of Polymer Engineering, Nanostructured Materials Research Center, Sahand University of Technology, Tabriz 51335-1996 (Iran, Islamic Republic of); Mohajerzadeh, Shams [Nano-Electronics and Thin Film Lab, School of Electrical and Computer Engineering, University of Tehran, P.O. Box 14395/515, Tehran (Iran, Islamic Republic of)

    2015-05-29

    The effect of different dopant anions on deposition and characteristics of polypyrrole (PPy) thin film has been studied in this work. Ultra-thin films of conducting PPy were deposited on insulating surfaces of glass and oxidized silicon wafer by in situ chemical polymerization in the presence of different anionic dopants including sodium dodecylbenzenesulfonate, sodium dodecyl sulfate, α-naphthalene sulfonic acid, anthraquinone-2-sulfonic acid sodium salt monohydrate/5-sulfosalicylic acid dehydrate, and camphor sulfonic acid. Hydrophilic/hydrophobic properties and morphology of the self-assembled monolayer of N-(3-trimethoxysilylpropyl)pyrrole, the surface modifying agent in this work, and PPy thin films were characterized before and after deposition by contact angle measurements, field emission scanning electron microscopy, and atomic force microscopy. Chemical structure, thickness, and conductivity of the thin films were also studied by attenuated total reflectance Fourier transform infrared spectrometer, ellipsometry, and four-point probe measurements. The results showed deposition of thin films of conducting PPy with comparable thickness in the range of 6-31 nm and different morphologies, uniformity, and smoothness with average roughness in the range of 0.3-6 nm and relatively high range of conductivity on the modified surfaces. - Highlights: • Conducting thin films of polypyrrole were deposited on glass and SiO{sub 2} substrates. • Surface modification using pyrrole-silane was employed prior to polymerization. • Films as thin as ≈ 7 nm were deposited using different surfactant/counter ions. • Chemistry of the counter ion affects thickness, conductivity and morphology. • Lower thickness/higher conductivity were obtained by structurally flexible dopants.

  19. Effect of nickel oxide seed layers on annealed-amorphous titanium oxide thin films prepared using plasma-enhanced chemical vapor deposition

    International Nuclear Information System (INIS)

    The effect of a nickel oxide (NiOx) seed layer on the crystallization and photocatalytic activity of the sequentially plasma-enhanced chemical vapor deposited amorphous titanium oxide (TiOx) thin film processed by a post-annealing process was investigated. The evolution of the crystalline structures, chemical bond configurations, and surface/cross-sectional morphologies of the annealed TiOx films, with and without a NiOx seed layer, was examined using X-ray diffractometer, Fourier transform infrared spectrometry, X-ray photoelectron spectroscopy, atomic force microscopy, and field emission scanning electron microscope measurements. Thermo- and photo-induced hydrophilicity was determined by measuring the contact angle of water droplet. Photocatalytic activity after UV light irradiation was evaluated from the decolorization of a methylene blue solution. The crystallization temperature of the TiOx film, deposited on a NiOx seed layer, was found to be lower than that of a pure TiOx film, further improving the thermo- and photo-induced surface super-hydrophilicity. The TiOx film deposited onto the NiOx seed layer, resulting in significant cluster boundaries, showed a rough surface morphology and proved to alleviate the anatase crystal growth by increasing the post-annealing temperature, which yielded a more active surface area and prohibited the recombination of photogenerated electrons and holes. The photocatalytic activity of the NiOx/TiOx system with such a textured surface therefore was enhanced and optimized through an adequate post-annealing process.

  20. Amorphous silicon carbon films prepared by hybrid plasma enhanced chemical vapor/sputtering deposition system: Effects of r.f. power

    International Nuclear Information System (INIS)

    Silicon carbon films were deposited using a hybrid radio frequency (r.f.) plasma enhanced chemical vapor deposition (PECVD)/sputtering deposition system at different r.f. powers. This deposition system combines the advantages of r.f. PECVD and sputtering techniques for the deposition of silicon carbon films with the added advantage of eliminating the use of highly toxic silane gas in the deposition process. Silicon (Si) atoms were sputtered from a pure amorphous silicon (a-Si) target by argon (Ar) ions and carbon (C) atoms were incorporated into the film from C based growth radicals generated through the discharge of methane (CH4) gas. The effects of r.f. powers of 60, 80, 100, 120 and 150 W applied during the deposition process on the structural and optical properties of the films were investigated. Raman spectroscopic studies showed that the silicon carbon films contain amorphous silicon carbide (SiC) and amorphous carbon (a-C) phases. The r.f. power showed significant influence on the C incorporation in the film structure. The a-C phases became more ordered in films with high C incorporation in the film structure. These films also produced high photoluminescence emission intensity at around 600 nm wavelength as a result of quantum confinement effects from the presence of sp2 C clusters embedded in the a-SiC and a-C phases in the films. - Highlights: ► Effects of radio frequency (r.f.) power on silicon carbon (SiC) films were studied. ► Hybrid plasma enhanced chemical vapor deposition/sputtering technique was used. ► r.f. power influences C incorporation in the film structure. ► High C incorporation results in higher ordering of the amorphous C phase. ► These films produced high photoluminescence emission intensity

  1. Chemical and microstructural study in radio frequency sputtered CdTe oxide films prepared at different N{sub 2}O pressures. Oxygen incorporation and film resputtering

    Energy Technology Data Exchange (ETDEWEB)

    Caballero-Briones, F. [CICATA-IPN Unidad Altamira, Km 14.5 Carretera Tampico-Puerto Industrial Altamira, 89600, Altamira, Tamps (Mexico)], E-mail: fcaballerobriones@ub.edu; Oliva, A.I.; Bartolo-Perez, P. [Applied Physics Department, CINVESTAV-IPN Unidad Merida, A.P. 73 Cordemex, 97310 Merida, Yucatan (Mexico); Zapata-Navarro, A. [CICATA-IPN Unidad Legaria, Legaria 694 Col. Irrigacion 11500, Mexico, D.F. (Mexico); Pena, J.L. [Applied Physics Department, CINVESTAV-IPN Unidad Merida, A.P. 73 Cordemex, 97310 Merida, Yucatan (Mexico)

    2008-10-01

    CdTe oxide films were grown by radio frequency sputtering in Ar-N{sub 2}O plasma at different N{sub 2}O partial pressures. The film oxygen content determined by Auger electron spectroscopy ranged from 15 to 60 at.%. The free O{sub 2} production during film deposition was monitored by in situ mass spectroscopy and it was found that it increases linearly over a critical N{sub 2}O pressure {approx} 4.7 x 10{sup -3} Pa alike the oxygen in the films. Film microstructure was studied by Raman spectroscopy and atomic force microscopy. Evidence of bands related to terminal Te-O vibrations was found in films prepared below the N{sub 2}O critical pressure, becoming predominant in films with higher oxygen content. The morphology and roughness evolution of the films confirm that they consist of a mixture of phases. Surface structures of the Ia-type and of the Ib-type were observed below and above the critical N{sub 2}O pressure. Eventually, ion bombardment process caused film resputtering.

  2. Chemical and microstructural study in radio frequency sputtered CdTe oxide films prepared at different N2O pressures. Oxygen incorporation and film resputtering

    International Nuclear Information System (INIS)

    CdTe oxide films were grown by radio frequency sputtering in Ar-N2O plasma at different N2O partial pressures. The film oxygen content determined by Auger electron spectroscopy ranged from 15 to 60 at.%. The free O2 production during film deposition was monitored by in situ mass spectroscopy and it was found that it increases linearly over a critical N2O pressure ∼ 4.7 x 10-3 Pa alike the oxygen in the films. Film microstructure was studied by Raman spectroscopy and atomic force microscopy. Evidence of bands related to terminal Te-O vibrations was found in films prepared below the N2O critical pressure, becoming predominant in films with higher oxygen content. The morphology and roughness evolution of the films confirm that they consist of a mixture of phases. Surface structures of the Ia-type and of the Ib-type were observed below and above the critical N2O pressure. Eventually, ion bombardment process caused film resputtering

  3. Studies on structural and thermo-chemical behavior of MFe12O19(s) (M = Sr, Ba and Pb) prepared by citrate-nitrate gel combustion method

    International Nuclear Information System (INIS)

    The citrate-nitrate gel combustion route was used to prepare SrFe12O19(s), BaFe12O19(s) and PbFe12O19(s). The compounds were characterized by Rietveld profile analysis of the X-ray powder diffraction data. The thermal expansion coefficients of MFe12O19 (M = Sr, Ba and Pb) were determined using high temperature powder X-ray diffraction data. The lattice parameters of these compounds were fitted into polynomial expressions as a function of temperature. Melting points of MFe12O19 (M = Sr, Ba and Pb) were determined using high temperature calorimeter and the values are; 1632 K, 1611 K and 1538 K, respectively. Standard molar heat capacities of BaFe12O19(s) and PbFe12O19(s) were determined from 130 K to 850 K using a heat flux type differential scanning calorimeter (DSC) and heat capacity anomalies were observed at 725 K and 718 K, respectively. This heat capacity anomaly is due to the magnetic order-disorder transition from ferrimagnetic state to paramagnetic state

  4. Enhanced photoluminescence and Raman properties of Al-Doped ZnO nanostructures prepared using thermal chemical vapor deposition of methanol assisted with heated brass.

    Directory of Open Access Journals (Sweden)

    Tamil Many K Thandavan

    Full Text Available Vapor phase transport (VPT assisted by mixture of methanol and acetone via thermal evaporation of brass (CuZn was used to prepare un-doped and Al-doped zinc oxide (ZnO nanostructures (NSs. The structure and morphology were characterized by field emission scanning electron microscopy (FESEM and x-ray diffraction (XRD. Photoluminescence (PL properties of un-doped and Al-doped ZnO showed significant changes in the optical properties providing evidence for several types of defects such as zinc interstitials (Zni, oxygen interstitials (Oi, zinc vacancy (Vzn, singly charged zinc vacancy (VZn-, oxygen vacancy (Vo, singly charged oxygen vacancy (Vo+ and oxygen anti-site defects (OZn in the grown NSs. The Al-doped ZnO NSs have exhibited shifted PL peaks at near band edge (NBE and red luminescence compared to the un-doped ZnO. The Raman scattering results provided evidence of Al doping into the ZnO NSs due to peak shift from 145 cm-1 to an anomalous peak at 138 cm-1. Presence of enhanced Raman signal at around 274 and 743 cm-1 further confirmed Al in ZnO NSs. The enhanced D and G band in all Al-doped ZnO NSs shows possible functionalization and doping process in ZnO NSs.

  5. Enhanced photoluminescence and Raman properties of Al-Doped ZnO nanostructures prepared using thermal chemical vapor deposition of methanol assisted with heated brass.

    Science.gov (United States)

    Thandavan, Tamil Many K; Gani, Siti Meriam Abdul; San Wong, Chiow; Md Nor, Roslan

    2015-01-01

    Vapor phase transport (VPT) assisted by mixture of methanol and acetone via thermal evaporation of brass (CuZn) was used to prepare un-doped and Al-doped zinc oxide (ZnO) nanostructures (NSs). The structure and morphology were characterized by field emission scanning electron microscopy (FESEM) and x-ray diffraction (XRD). Photoluminescence (PL) properties of un-doped and Al-doped ZnO showed significant changes in the optical properties providing evidence for several types of defects such as zinc interstitials (Zni), oxygen interstitials (Oi), zinc vacancy (Vzn), singly charged zinc vacancy (VZn-), oxygen vacancy (Vo), singly charged oxygen vacancy (Vo+) and oxygen anti-site defects (OZn) in the grown NSs. The Al-doped ZnO NSs have exhibited shifted PL peaks at near band edge (NBE) and red luminescence compared to the un-doped ZnO. The Raman scattering results provided evidence of Al doping into the ZnO NSs due to peak shift from 145 cm-1 to an anomalous peak at 138 cm-1. Presence of enhanced Raman signal at around 274 and 743 cm-1 further confirmed Al in ZnO NSs. The enhanced D and G band in all Al-doped ZnO NSs shows possible functionalization and doping process in ZnO NSs. PMID:25756598

  6. Synthesis, structure and magnetic properties of Y3Fe5-xAlxO12 garnets prepared by the soft chemical method

    Directory of Open Access Journals (Sweden)

    Pedro Paulo Silva Ortega

    2014-12-01

    Full Text Available A study was undertaken about the structural, morphological and magnetic properties at room temperature of crystalline aluminium substituted yttrium iron garnet, YIG (Y3Fe5-xAlxO12 with 1.5< x <1.7 nanoparticles prepared by polymeric precursor method at the temperature of 700 °C for 2 hours. The single-phase character and the well-defined structure of YIG nanoparticles were confirmed by X-ray diffraction, excluding the presence of any other phases. The Raman spectra showed that the changes of lattice vibration would influence interaction between the Fe ion and the host. Mean crystallite size of the single-phase powder was about 46–65 nm. Particles’ morphology was investigated by high-resolution transmission electron microscopy, which shows that the particles were agglomerated. From hysteresis loops, particles’ efficiency range from 91.4% to 95.9% as Fe/Al ratio decreases. Saturation magnetization was affected by the particle size and Fe/Al stoichiometric ratio. We observe that the saturation magnetization increases as the Fe/Al ratio is raised due to enhancement of the surface spin effects.

  7. Preparation of diatomite/Ca(OH){sub 2} sorbents and modelling their sulphation reaction Istanbul Technical University, Istanbul (Turkey). Chemical and Metallurgical Engineering Faculty

    Energy Technology Data Exchange (ETDEWEB)

    Nilgun Karatepe; Nilufer Erdoan; Aysegul Ersoy-Mericboyu; Sadriye Kucukbayrak

    2004-09-01

    Mixtures of Ca(OH){sub 2} and diatomite were hydrated at different conditions to produce reactive SO{sub 2} sorbents. Two different hydration techniques were used; namely, atmospheric and pressure hydration. The effect of the hydration temperature, time and diatomite/Ca(OH){sub 2} weight ratio on the physical properties of the activated sorbents were investigated. In atmospheric hydration, it was found that increasing the temperature and hydration time caused an increase in the total surface area of the sorbents. However, surface area values of the sorbents prepared from mixtures which have different diatomite/Ca(OH){sub 2} weight ratio were generally not changed significantly. In pressure hydration, the surface area of the activated sorbents was positively affected from the hydration temperature and pressure. Finally, Ca(OH){sub 2} and two diatomite/Ca(OH){sub 2} sorbents were sulphated at constant temperature (338 K) using a synthetic gaseous mixture consisting of 5% O{sub 2}, 10% CO{sub 2}, 5000 ppm SO{sub 2} and the balance of nitrogen with a 55% relative humidity. The sulphation reaction of these sorbents were investigated and modelled. The unreacted shrinking core model was chosen to describe this non-catalytic solid/gas (hydrated sorbent/SO{sub 2}) reaction mechanism. The experimental results were found to be correlated successfully by this model.

  8. Wet chemical preparation of YVO4:Eu thin films as red-emitting phosphor layers for fully transparent flat dielectric discharge lamp

    International Nuclear Information System (INIS)

    Highly transparent YVO4:Eu thin films were deposited via dip coating of liquid nanoparticle dispersions on glass substrates. Annealing of the nanoparticle layers resulted in restructuring of the material into oriented crystalline films. The crystallinity was confirmed using powder X-ray diffraction. Film thickness was adjusted to 467 nm by multiple deposition. The resulting coatings show > 99% absorbance for wavelength below 300 nm and > 90% transmission in the visible spectral range. Under UV-light excitation a bright red photoluminescence with a quantum efficiency of 20% is observed. A planar, transparent dielectric barrier discharge lamp was constructed using YVO4:Eu coated glasses and transparent electrodes made from antimony-doped tin dioxide thin films. - Highlights: ► Preparation of highly transparent Eu3+ doped YVO4 phosphor thin films. ► Improved crystallinity and optical properties through heat treatment. ► Red emitting films on glass substrates were combined with antimony tin oxide thin films. ► Fully transparent, planar gas discharge lamp as prototype for a light emitting window.

  9. Preparation of YBa{sub 2}Cu{sub 3}O{sub 7-x} superconducting films: influence of the chemical composition on the sintering

    Energy Technology Data Exchange (ETDEWEB)

    Benavidez, E.; Quaranta, N.; Gonzalez Oliver, C.J.R.; Caruso, R. [FRSN, UTN, San Nicolas (Argentina). Desarrollo y Tecnologia de Materiales; de Sanctis, O. [Laboratorio de Materiales Ceramicos, FCEIyA, UNR-IFIR, Av. Pellegrini 250 (2000), Rosario (Argentina); Frattini, A. [Area Fisica-Dpto de Quimica Fisica-FCByF-UNR, Suipacha 531(2000), Rosario (Argentina)

    1999-12-01

    The influence of the cationic ratio Y:Ba:Cu on the kinetics of densification of the YBa{sub 2}Cu{sub 3}O{sub 7-x} (YBCO) superconductor ceramic was studied. The powders were prepared from organic precursors and the nominal compositions were: (A) stoichiometric composition YBa{sub 2}Cu{sub 3}O{sub 7-x}, (B) composition on the tie line joining YBa{sub 2}Cu{sub 3}O{sub 7-x}-BaCuO{sub 2} phases, and (C) composition in the triangle YBa{sub 2}Cu{sub 3}O{sub 7-x}-Y{sub 2}BaCuO{sub 5}-CuO. The phases present in these powders heated to 890 C were detected by X-ray diffraction (XRD), while the ratio Y:Ba:Cu was measured by neutronic activation analysis (NAA). The reactions between 900 C and 1070 C under O{sub 2} atmosphere were determined by differential thermal analysis (DTA) at a heating rate of 10 C/min. Compacts of different powders were obtained by uniaxial pressing and were then studied by dilatometric experiments under similar conditions as established in DTA measurements. The dilatometric curves were applied to different sintering models to obtain the validity ranges and activation energies corresponding to the different densification mechanisms that operate in the initial and intermediate stages of sintering. (orig.)

  10. Electrical characteristics of mixed Zr-Si oxide thin films prepared by ion beam induced chemical vapor deposition at room temperature

    International Nuclear Information System (INIS)

    Mixed Zr-Si oxide thin films have been prepared at room temperature by ion beam decomposition of organometallic volatile precursors. The films were flat and amorphous. They did not present phase segregation of the pure single oxides. A significant amount of impurities (-C-, -CHx, -OH, and other radicals coming from partially decomposed precursors) remained incorporated in the films after the deposition process. This effect is minimized if the Ar content in the O2/Ar bombarding gas is maximized. Static permittivity and breakdown electrical field of the films were determined by capacitance-voltage and current-voltage electrical measurements. It is found that the static permittivity increases non-linearly from ∼ 4 for pure SiO2 to ∼ 15 for pure ZrO2. Most of the dielectric failures in the films were due to extrinsic breakdown failures. The maximum breakdown electrical field decreases from ∼ 10.5 MV/cm for pure SiO2 to ∼ 45 MV/cm for pure ZrO2. These characteristics are justified by high impurity content of the thin films. In addition, the analysis of the conduction mechanisms in the formed dielectrics is consistent to Schottky and Poole-Frenkel emission for low and high electric fields applied, respectively.

  11. Optical and structural properties of microcrystalline GaN on an amorphous substrate prepared by a combination of molecular beam epitaxy and metal–organic chemical vapor deposition

    Science.gov (United States)

    Min, Jung-Wook; Hwang, Hyeong-Yong; Kang, Eun-Kyu; Park, Kwangwook; Kim, Ci-Hyun; Lee, Dong-Seon; Jho, Young-Dahl; Bae, Si-Young; Lee, Yong-Tak

    2016-05-01

    Microscale platelet-shaped GaN grains were grown on amorphous substrates by a combined epitaxial growth method of molecular beam epitaxy (MBE) and metal–organic chemical vapor deposition (MOCVD). First, MBE GaN was grown on an amorphous substrate as a pre-orienting layer and its structural properties were investigated. Second, MOCVD grown GaN samples using the different growth techniques of planar and selective area growth (SAG) were comparatively investigated by transmission electron microscopy (TEM), cathodoluminescence (CL), and photoluminescence (PL). In MOCVD planar GaN, strong bound exciton peaks dominated despite the high density of the threading dislocations (TDs). In MOCVD SAG GaN, on the other hand, TDs were clearly reduced with bending, but basal stacking fault (BSF) PL peaks were observed at 3.42 eV. The combined epitaxial method not only provides a deep understanding of the growth behavior but also suggests an alternative approach for the growth of GaN on amorphous substances.

  12. Effect of copper doping on structural, optical and electrical properties of Cd0.8Zn0.2S films prepared by chemical bath deposition

    Indian Academy of Sciences (India)

    K Hadasa; G Yellaiah; M Nagabhushanam

    2014-02-01

    Cd0.8Zn0.2S:Cu films of 1.3–6.1 mole percentage of copper have been grown on mica substrate by using chemical bath deposition technique. The films have been characterized by using XRD, SEM and UV spectrophotometer. X-ray diffraction studies have shown that the films are polycrystalline. The average crystallite size as measured from XRD data is in the range of 125–130 nm. The activation energies of Cd0.8Zn0.2S:Cu films, as observed from d.c. conductivity studies in the temperature range (77–300 K) studied, decreased with the increase in Cu concentration. The optical absorption studies have revealed that the energy gap increases gradually with an increase in Cu concentration, whereas conductivity studies have shown an anomalous increase in conductivity in films of 3.8 mole percentage of Cu. SEM pictures have revealed the presence of defects with spherical structure having fibre network. The variation of electrical conductivity is explained based on the defects present and by adopting tunneling mechanism.

  13. Modified DLC coatings prepared in a large-scale reactor by dual microwave/pulsed-DC plasma-activated chemical vapour deposition

    International Nuclear Information System (INIS)

    Diamond-Like Carbon (DLC) films find abundant applications as hard and protective coatings due to their excellent mechanical and tribological performances. The addition of new elements to the amorphous DLC matrix tunes the properties of this material, leading to an extension of its scope of applications. In order to scale up their production to a large plasma reactor, DLC films modified by silicon and oxygen additions have been grown in an industrial plant of 1m3 by means of pulsed-DC plasma-activated chemical vapour deposition (PACVD). The use of an additional microwave (MW) source has intensified the glow discharge, partly by electron cyclotron resonance (ECR), accelerating therefore the deposition process. Hence, acetylene, tetramethylsilane (TMS) and hexamethyldisiloxane (HMDSO) constituted the respective gas precursors for the deposition of a-C:H (DLC), a-C:H:Si and a-C:H:Si:O films by dual MW/pulsed-DC PACVD. This work presents systematic studies of the deposition rate, hardness, adhesion, abrasive wear and water contact angle aimed to optimize the technological parameters of deposition: gas pressure, relative gas flow of the monomers and input power. This study has been completed with measures of the atomic composition of the samples. Deposition rates around 1 μm/h, typical for standard processes held in the large reactor, were increased about by a factor 10 when the ionization source has been operated in ECR mode

  14. Effects of growth parameters on the yield and morphology of Si{sub 3}N{sub 4} microcoils prepared by chemical vapor deposition

    Energy Technology Data Exchange (ETDEWEB)

    Du, Hongli, E-mail: hongli_du@126.com [Institute of Material Science and Engineering, Shijiazhuang University of Economics, Shijiazhuang 050031 (China); Zhang, Wei [Institute of Hydrogeology and Environmental Geology, Chinese Academy of Geological Sciences, Shijiazhuang 050061 (China); Li, Yan [Institute of Material Science and Engineering, Shijiazhuang University of Economics, Shijiazhuang 050031 (China)

    2014-02-01

    Highlights: • CVD method was successfully applied to obtain Si{sub 3}N{sub 4} microcoils in high yield without the presence of catalyst. • The process was systematically investigated through a series of control experiments. • The effects of synthesis parameters on the yield and morphology of Si{sub 3}N{sub 4} microcoils were found. • The growth mechanism of the Si{sub 3}N{sub 4} microcoils could be explained by the different growth rates between the amorphous layer and the crystalline layer. - Abstract: In this study, we provided a reliable chemical vapor deposition (CVD) method to synthesize high-purity Si{sub 3}N{sub 4} microcoils in high yield without the presence of catalyst. The achieved products were characterized by X-ray diffraction, scanning electron microscopy, and transmission electron microscope. The results indicated that the yield and morphology of Si{sub 3}N{sub 4} products were influenced by the synthesis parameters such as reaction temperature, reaction time and gas flow rate. The particular conditions favorable to high yield synthesis of Si{sub 3}N{sub 4} microcoils were obtained through a series of control experiments. Furthermore, the growth of Si{sub 3}N{sub 4} microcoils was supposed to be in accord with vapor-solid (VS) growth process and the different growth rates between the amorphous layer and the crystalline layer were used to explain the formation of the coil geometry.

  15. Effect of reaction time on structural, morphology and optical properties of ZnO nanoflakes prepared by chemical bath deposition method

    International Nuclear Information System (INIS)

    ZnO nanoflakes have been successfully synthesized by the chemical bath deposition (CBD) method for different reaction times. X-ray diffraction (XRD) results confirm the initial formation of the cubic ZnO structure. However, increasing the reaction time resulted into the emergence of the well-known hexagonal wurtzite structure of ZnO. Scanning electron microscopy images showed the presence of agglomerated nanoflakes. The morphology was found not to depend on synthesis time. UV–vis spectra showed a partially increase in the percentage reflectance and the absorption edges red shifted to the higher wavelength with an increase in synthesis time. The highest band gap energy was obtained for ZnO synthesized for 1 min, with its estimated band gap energy of 3.91±0.08 eV. The estimated band gap decreased with an increase in the reaction time. The photoluminescent intensity of the emission peak at 473 nm decreased with an increase in reaction time.

  16. Petal-like CuO nanostructures prepared by a simple wet chemical method, and their application to non-enzymatic amperometric determination of hydrogen peroxide

    International Nuclear Information System (INIS)

    Uniform and petal-like CuO nanostructures have been deposited on a copper foil substrate by a simple wet chemical method at room temperature through oxidation of elemental copper in strongly alkaline solution. The concentration of NaOH in the precursor solution is critical for the product morphology. The morphology of the CuO nanostructures was characterized by scanning electron microscopy and their crystal structure was studied by X-ray diffraction. Their electrochemical performance was evaluated by cyclic voltammetry, amperometry, and electrochemical impedance spectroscopy. The CuO films are shown to represent active electrode materials for non-enzymatic amperometric determination of H2O2. Response to H2O2 in solutions of pH 7.4 at a working potential of −200 mV (vs. Ag/AgCl) is linear in the 10 to 960 μM concentration range, with the detection limit 2.1 μM and the sensitivity 5030 μA∙mM−1. Its excellent electrocatalytic activity, large specific surface area, efficient mass transport and electron transfer properties make this electrode a highly sensitive and reliable tool for electrochemical determination of H2O2. (author)

  17. Porous Silicon & Titanium Dioxide Coatings Prepared by Atmospheric Pressure Plasma Jet Chemical Vapour Deposition Technique-A Novel Coating Technology for Photovoltaic Modules

    Directory of Open Access Journals (Sweden)

    S. Bhatt

    2011-01-01

    Full Text Available Atmospheric Pressure Plasma Jet (APPJ is an alternative for wet processes used to make anti reflection coatings and smooth substrate surface for the PV module. It is also an attractive technique because of it’s high growth rate, low power consumption, lower cost and absence of high cost vacuum systems. This work deals with the deposition of silicon oxide from hexamethyldisiloxane (HMDSO thin films and titanium dioxide from tetraisopropyl ortho titanate using an atmospheric pressure plasma jet (APPJ system in open air conditions. A sinusoidal high voltage with a frequency between 19-23 kHz at power up to 1000 W was applied between two tubular electrodes separated by a dielectric material. The jet, characterized by Tg ~ 600-800 K, was mostly laminar (Re ~ 1200 at the nozzle exit and became partially turbulent along the jet axis (Re ~ 3300. The spatially resolved emission spectra showed OH, N2, N2+ and CN molecular bands and O, H, N, Cu and Cr lines as well as the NO2 chemiluminescence continuum (450-800 nm. Thin films with good uniformity on the substrate were obtained at high deposition rate, between 800 -1000 nm.s-1, and AFM results revealed that coatings are relatively smooth (Ra ~ 2 nm. The FTIR and SEM analyses were better used to monitor the chemical composition and the morphology of the films in function of the different experimental conditions.

  18. Structure, mechanical, and frictional properties of hydrogenated fullerene-like amorphous carbon film prepared by direct current plasma enhanced chemical vapor deposition

    Science.gov (United States)

    Wang, Yongfu; Gao, Kaixiong; Zhang, Junyan

    2016-07-01

    In this study, fullerene like carbon (FL-C) is introduced in hydrogenated amorphous carbon (a-C:H) film by employing a direct current plasma enhanced chemical vapor deposition. The film has a low friction and wear, such as 0.011 and 2.3 × 10-9mm3/N m in the N2, and 0.014 and 8.4 × 10-8mm3/N m in the humid air, and high hardness and elasticity (25.8 GPa and 83.1%), to make further engineering applications in practice. It has several nanometers ordered domains consisting of less frequently cross-linked graphitic sheet stacks. We provide new evidences for understanding the reported Raman fit model involving four vibrational frequencies from five, six, and seven C-atom rings of FL-C structures, and discuss the structure evolution before or after friction according to the change in the 1200 cm-1 Raman band intensity caused by five- and seven-carbon rings. Friction inevitably facilitates the transformation of carbon into FL-C nanostructures, namely, the ultra low friction comes from both such structures within the carbon film and the sliding induced at friction interface.

  19. Dielectric properties of Ca(Zr0.05Ti0.95)O3 thin films prepared by chemical solution deposition

    International Nuclear Information System (INIS)

    Ca(Zr0.05Ti0.95)O3 (CZT) thin films were grown on Pt(111)/Ti/SiO2/Si(100) substrates by the soft chemical method. The films were deposited from spin-coating technique and annealed at 928K for 4h under oxygen atmosphere. CZT films present orthorhombic structure with a crack free and granular microstructure. Atomic force microscopy and field-emission scanning electron microscopy showed that CZT present grains with about 47nm and thickness about 450nm. Dielectric constant and dielectric loss of the films was approximately 210 at 100kHz and 0.032 at 1MHz. The Au/CZT/Pt capacitor shows a hysteresis loop with remnant polarization of 2.5μC/cm2, and coercive field of 18kV/cm, at an applied voltage of 6V. The leakage current density was about 4.6x10-8A/cm2 at 3V. Dielectric constant-voltage curve is located at zero bias field suggesting the absence of internal electric fields

  20. Influence of Fe-doped on structural, electronic structural and optical properties of hydrogenated amorphous carbon films prepared by plasma enhanced chemical vapor deposition

    International Nuclear Information System (INIS)

    Fe-doped hydrogenated amorphous carbon (a-C:H:Fe) films were deposited from an isobutene/ferrocene/H2 gas mixture by plasma enhanced chemical metal organic vapor deposition. Raman spectra were used to characterize the bonding structure of the a-C:H:Fe films and hydrogenated amorphous carbon (a-C:H) films. Optical properties were investigated by the UV-vis spectroscopy and the photoluminescence spectra. The number of six-numbered rings of the a-C:H films increases and sp2 clustering of the films decreases after Fe-doping. The Tauc optical gap of the a-C:H:Fe films becomes narrower by 0.15-0.23 eV relative to the value of the a-C:H films. The narrowing of the optical gap after doping is attributed primarily to the extended state around the Fe deep level in the band gap and the narrowing of the π and π* band edge states because of the increase of the number of six-numbered rings in the a-C:H films. Fe deep level defects of the a-C:H:Fe films contribute chiefly to non-radiative recombination.

  1. Optical and Structural Properties of Microcrystalline GaN on an Amorphous Substrate Prepared by a Combination of Molecular Beam Epitaxy and Metal-Organic Chemical Vapor Deposition

    Energy Technology Data Exchange (ETDEWEB)

    Min, Jung-Wook; Hwang, Hyeong-Yong; Kang, Eun-Kyu; Park, Kwangwook; Kim, Ci-Hyun; Lee, Dong-Seon; Jho, Young-Dahl; Bae, Si-Young; Lee, Yong-Tak

    2016-05-01

    Microscale platelet-shaped GaN grains were grown on amorphous substrates by a combined epitaxial growth method of molecular beam epitaxy (MBE) and metal-organic chemical vapor deposition (MOCVD). First, MBE GaN was grown on an amorphous substrate as a pre-orienting layer and its structural properties were investigated. Second, MOCVD grown GaN samples using the different growth techniques of planar and selective area growth (SAG) were comparatively investigated by transmission electron microscopy (TEM), cathodoluminescence (CL), and photoluminescence (PL). In MOCVD planar GaN, strong bound exciton peaks dominated despite the high density of the threading dislocations (TDs). In MOCVD SAG GaN, on the other hand, TDs were clearly reduced with bending, but basal stacking fault (BSF) PL peaks were observed at 3.42 eV. The combined epitaxial method not only provides a deep understanding of the growth behavior but also suggests an alternative approach for the growth of GaN on amorphous substances.

  2. Correlation between optical properties and Si nanocrystal formation of Si-rich Si oxide films prepared by plasma-enhanced chemical vapor deposition

    International Nuclear Information System (INIS)

    We have investigated the phase separation and silicon nanocrystal (Si NC) formation in correlation with the optical properties of Si suboxide (SiO x, 0 x films were deposited by plasma-enhanced chemical vapor deposition at different nitrous oxide/silane (N2O/SiH4) flow ratios. The as-deposited films show increased Si concentration with decreasing N2O/SiH4 flow ratio, while the deposition rate and surface roughness have strong correlations with the flow ratio in the N2O/SiH4 reaction. After thermal annealing at temperatures above 1000 deg. C, Fourier transform infrared spectroscopy, Raman spectroscopy, and transmission electron microscopy manifest the progressive phase separation and continuous growth of crystalline-Si (c-Si) NCs in the SiO x films with increasing annealing temperature. We observe a transition from multiple-peak to single peak of the strong red-range photoluminescence (PL) with increasing Si concentration and annealing temperature. The appearance of the single peak in the PL is closely related to the c-Si NC formation. The PL also redshifts from ∼1.9 to 1.4 eV with increasing Si concentration and annealing temperature (i.e., increasing NC size). The good agreements of the PL evolution with NC formation and the PL peak energy with NC size distribution support the quantum confinement model

  3. Effect of rapid thermal annealing on the structural and electrical properties of solid ZnO/NiO heterojunctions prepared by a chemical solution process

    International Nuclear Information System (INIS)

    Transparent pn-heterojunction electrodes composed of n-type zinc oxide (ZnO) nanorod arrays and p-type NiO are fabricated by a chemical solution route combined with rapid thermal annealing (RTA). The effects of RTA treatment (450 °C, 1 min) in reducing atmosphere on the structural properties and alignment of the ZnO nanorods are investigated. SEM images and XRD patterns show that the average diameter and length are increased, and the alignment and crystal quality of the nanorod arrays are significantly improved. The RTA-treated ZnO shows uniform and well-aligned nanorod arrays with a high aspect ratio of ∼12.4. The structural improvements associated with ZnO crystalline and defect reduction are further verified from the enhanced UV to visible emission ratio by a photoluminescence analysis. Moreover, the effect of RTA on the I-V characteristics of the ZnO/NiO heterojunction electrodes is also investigated; the electrical parameters of the junction are determined from the forward-bias I-V characteristics using Cheung's method. The results reveal that the series resistance is significantly reduced from 784.4 to 114.8 Ω, which leads to better rectifying behaviour with rectifying slope increased to ∼6.67 mA V-1. The RTA-processed ZnO/NiO heterojunctions with excellent optoelectronic properties may find wide applications in sensors and solid-state oxide junction-based devices. (paper)

  4. Parametric optimisation of core–shell ZnS:Mn/ZnS nanoparticles prepared by ultrasound-controlled wet chemical route

    International Nuclear Information System (INIS)

    Core–shell type manganese-doped zinc sulphide nanoparticles ZnS:Mn/ZnS, showing strong absorption of ultraviolet light in the 280–450 nm range and emitting orange-yellow light close to 600 nm, were synthesised for eventual deployment as wavelength down-shifters for solar cells. While most syntheses described in literature employed long reaction times and high reaction/annealing temperatures in excess of 100 °C, this work presents a facile low-temperature wet chemical route. Key synthesis parameters – including zinc to sulphur ratio, manganese doping percentage, reaction sequence and ultrasonication time – were optimised systematically to achieve optimum orange emission intensity. Nanoparticles with average size ∼2.3 nm and showing bright orange emission under UV excitation were ultimately achieved. Various characterisation techniques, namely HRTEM, XRD, ICP, ESR, UV–visible absorption spectrometry and fluorescence spectroscopy, were used to probe the nature of the sample. -- Highlights: • Shell formation achieved by ultrasonic decomposition of zinc–thiourea complex. • Optimal zinc to sulphur ratio in reaction mix was found to be 1:1.2. • Optimal manganese doping percentage was found to be 5.8%. • Addition of cationic precursors to anionic precursors proved to be favourable. • Ultrasonication times exceeding 15 min were detrimental to emission intensity

  5. Structural, optical and electrical properties of Cu2FeSnX4 (X = S, Se) thin films prepared by chemical spray pyrolysis

    International Nuclear Information System (INIS)

    Highlights: • CFTS(Se) thin films have been synthesized by low-cost spray-based deposition. • The fabricated films were found to be of stannite structure and p-type conductivity. • Band gaps of CFTS and CFTSe thin films are 1.37 and 1.11 eV, respectively. - Abstract: We report on fabrication of polycrystalline Cu2FeSnX4 (X = S, Se) thin films by chemical spray pyrolysis subsequent with post-sulfurization and selenization. The post-annealing of as-sprayed Cu2FeSnS4 (CFTS) films in sulfur and selenium ambient demonstrated drastically improved surface texture as well as crystallinity. The crystal lattice parameters calculated from X-ray diffraction patterns for post-annealed films were found to be consistent with stannite structure. The fabricated Cu2FeSnS4 (CFTS) and Cu2FeSnSe4 (CFTSe) films showed p-type conductivity with carrier concentration in the range of 1021 cm−3 and mobility ∼1–5 cm2 V−1 s−1. The band gap energies of post-sulfurized CFTS and post-selenized CFTSe films were estimated to be ∼1.37 eV and ∼1.11 eV with an error of ±0.02 eV by UV–Vis absorption, respectively, which are promising for photovoltaic application

  6. Structural, optical and electrical properties of Cu{sub 2}FeSnX{sub 4} (X = S, Se) thin films prepared by chemical spray pyrolysis

    Energy Technology Data Exchange (ETDEWEB)

    Khadka, Dhruba B.; Kim, JunHo, E-mail: jhk@inu.ac.kr

    2015-07-25

    Highlights: • CFTS(Se) thin films have been synthesized by low-cost spray-based deposition. • The fabricated films were found to be of stannite structure and p-type conductivity. • Band gaps of CFTS and CFTSe thin films are 1.37 and 1.11 eV, respectively. - Abstract: We report on fabrication of polycrystalline Cu{sub 2}FeSnX{sub 4} (X = S, Se) thin films by chemical spray pyrolysis subsequent with post-sulfurization and selenization. The post-annealing of as-sprayed Cu{sub 2}FeSnS{sub 4} (CFTS) films in sulfur and selenium ambient demonstrated drastically improved surface texture as well as crystallinity. The crystal lattice parameters calculated from X-ray diffraction patterns for post-annealed films were found to be consistent with stannite structure. The fabricated Cu{sub 2}FeSnS{sub 4} (CFTS) and Cu{sub 2}FeSnSe{sub 4} (CFTSe) films showed p-type conductivity with carrier concentration in the range of 10{sup 21} cm{sup −3} and mobility ∼1–5 cm{sup 2} V{sup −1} s{sup −1}. The band gap energies of post-sulfurized CFTS and post-selenized CFTSe films were estimated to be ∼1.37 eV and ∼1.11 eV with an error of ±0.02 eV by UV–Vis absorption, respectively, which are promising for photovoltaic application.

  7. Effects of radio-frequency power on the properties of carbon thin films prepared by thermal chemical vapor deposition enhanced with remote inductively-coupled-plasma using acetylene/nitrogen mixtures

    International Nuclear Information System (INIS)

    The effects of radio-frequency (rf) power on the properties of carbon thin films prepared by thermal chemical vapor deposition (CVD) enhanced with remote inductively-coupled-plasma (ICP) are investigated. Acetylene and nitrogen were used as the precursor gases, and rf-powers of ICP were set as 0, 100, 200, 300, and 400 W. The deposition temperature, working pressure, and deposition time were set as 1248 K, 4 kPa, and 2 h, respectively. The residual gases, film thicknesses, microstructures, chemical characteristics, mechanical properties, and electrical properties of carbon thin films were investigated by residual gas analyzer (RGA), field emission scanning electron microscopy, X-ray diffractometer (and Raman scattering spectrometer), X-ray photoelectron spectrometer, nanoindenter, and four point probe, respectively. RGA results reveal that the main species in the gas phase contain H2, C2H, C2H2, HCN (or C2H3), and N2 (or C2H4). Moreover, C2H, C2H2, and C2H4 can be speculated as the main species for carbon thin film deposition. As the rf-power increases from 0 to 400 W, the deposition rate of carbon thin films decreases from 204 to 36.0 nm/h. The crystallinity and ordering degree of carbon thin films increase with increasing rf-power from 0 to 400 W, but the ratio of sp2 carbon sites in carbon thin films decreases from 95 to 75%. The Young's modulus, hardness, and electrical resistivity of carbon thin films increase with increasing rf-power. Furthermore, the effects of rf-power on the deposition rates of carbon thin films prepared by thermal CVD enhanced with remote ICP using C2H2/N2 and CH4/N2 mixtures are compared. - Highlights: • Carbon films are prepared by TCVD enhanced with remote ICP using C2H2/N2 mixtures. • The deposition rate of carbon thin films decreases with increasing the rf-power. • C2H, C2H2, and C2H4 are speculated as the main species for carbon film deposition. • The sp2 sites in carbon thin films decrease with increasing rf-power.

  8. Preparation of 1-bromoheptacosane

    International Nuclear Information System (INIS)

    Alkybromides are ones of the main organic precursors for fatty acids and alcohols labelling with Carbon 1-14. In this work the preparation of 1-bromoheptacosane by bromodescarboxylation of 1-octacosanoic acid is described. The synthesis yielded 80.5% of final product and more than 97% of chemical purity. Clean-up procedure modifications and spectral data bromoheptacosane are also reported

  9. 控释肥包衣剂的制备及理化性质研究%Studies on Preparation and Physico-chemical Properties of Coating-agent for Controlled Release Fertilizer

    Institute of Scientific and Technical Information of China (English)

    刘英; 熊海蓉; 祝友; 熊远福; 李霞; 刘俊

    2013-01-01

      为了获得控释肥包衣剂的制备条件、探明其理化性质,以2种树脂为成膜材料,探讨了成膜材料复合比、成膜材料用量、增塑剂用量、乳化剂用量等单因素对控释肥包衣剂制备效果的影响,运用正交试验L9(34)确定了控释肥包衣剂制备的最佳条件;并对其pH、粘度、成膜时间、成膜性、衣膜水溶性、包衣均匀度、包衣脱落率等理化性质进行了测定。结果表明,控释肥包衣剂的最佳制备条件:树脂JZ与BZ复合比1:1.5,成膜材料用量12%,增塑剂用量0.8%,乳化剂用量1.0%,色素用量0.08%,乙酸乙酯用量86.12%。理化性质测定结果显示:pH 5.21,粘度为21.1 MPa/s,成膜性良好,衣膜不溶于水,成膜时间为6 min,包衣均匀度95%,包衣脱落率<8%,表明所制备的控释肥包衣剂理化性质良好。%To obtain the preparation conditions and explore the physico-chemical properties of coating-agent for controlled release fertilizer, the single factor tests of the composite ratio of film-forming materials, the amount of film-forming materials, plasticizer, emulsifier and pigment were made with two resins as the film-forming materials, and the optimal preparation conditions of coating-agent for controlled-fertilizer were determined by orthogonal test L9(34). The physico-chemical properties of the pH, viscosity, film-forming time, film-forming properties, water solubility of coated film, coating uniformity, coating-off rate were measured. The results showed that, the optimal preparation conditions were as follows:the composite ratio (JZ:BZ) was 1:1.5, amount of film-forming materials was 12%, plasticizer was 0.8%, emulsifier was 1.0%, pigment was 0.08% and solvent was 86.12%. Test results of physico-chemical properties showed that, the pH was 5.21, viscosity was 21.1 MPa/s, the film was good and indissolvable in water, the film-forming time was 6 min, coating uniformity was 95%, coating

  10. Sucos de laranja industrializados e preparados sólidos para refrescos: estabilidade química e físico-química Industrialized orange juices and refreshment prepared from orange juice powder: chemical and physicochemical stability

    Directory of Open Access Journals (Sweden)

    Patricia T. Silva

    2005-09-01

    Full Text Available O suco de laranja in natura é considerado uma das melhores fontes de vitamina C da dieta. No entanto, o ritmo de vida acelerado da sociedade atual associado à praticidade de preparo e armazenamento tem levado ao aumento do consumo de sucos e refrescos industrializados, porém pouco se conhece sobre a estabilidade destes produtos. Com o objetivo de avaliar a estabilidade de sucos de laranja prontos para o consumo (SPC e de refrescos elaborados a partir de preparados sólidos (PSR, foram determinados os teores de ácido ascórbico (AA e de sólidos solúveis totais (SST, a acidez total titulável (ATT e o pH. O teor de AA dos SPC variou de 17,25mg% a 62,40mg% (p = 0,05. Duas amostras apresentaram teor de AA inferior ao mínimo estabelecido pela legislação. Para os refrescos elaborados a partir dos PSR, o teor de AA variou entre 0,67mg% e 32,00mg% (p = 0,05. O pH e o teor de SST mantiveram-se constantes, enquanto que a ATT apresentou variações durante o armazenamento. Os SPC podem ser considerados como fonte de vitamina C, ao contrário da maioria dos refrescos elaborados a partir dos PSR que não podem ser considerados fontes importantes desta vitamina.Fresh orange juice is considered to be one of the best sources of vitamin C. Nevertheless, hand squeezed juice is often inconvenient for consumers who seek practical and fast ways to prepare their meals. The objective of this study was to analyze the chemical and physicochemical stability of ready to drink and refreshments prepared from orange juice powder commercially available in the city of Rio de Janeiro. The ascorbic acid (AA content, total soluble solids (TSS, total tritatable acidity (TAA and pH were determined. The AA content of ready to drink orange juice ranged from 17.25mg% to 62.40mg (p = 0.05. In two batches the AA content was lower than that established by the Brazilian legislation. The AA content of refreshments prepared from orange juice powder ranged from 0.67mg% to 32.00mg

  11. Synthesis and study of structural, dielectric, magnetic and magnetoelectric characterization of BiFeO3–NiFe2O4 nanocomposites prepared by chemical solution method

    International Nuclear Information System (INIS)

    Highlights: • Synthesized nanocomposites of xNiFe2O4–(1−x)BiFeO3 (x = 0.1, 0.2, 0.3, 0.4). • The average particles size is around 30–70 nm. • Anomaly in dielectric constant is a signature of magnetoelectric coupling (γ). • γ calculated from fractional change of Δε ∼ γM2 by varying magnetic field. • Magnetic properties greatly enhanced with increase in nickel ferrite content. -- Abstract: Magnetoelectric (ME) nanocomposites of xNiFe2O4–(1−x)BiFeO3 (x = 0.1, 0.2, 0.3, 0.4) have been prepared by chemical solution method. The samples have been calcined at various temperatures ranging from 500 to 700 °C and X-ray diffraction analysis showed phase formation of xNiFe2O4–(1−x)BiFeO3 nanocomposites calcined at 500 °C. The effect of annealing temperature on structural and magnetic properties was studied. TEM shows the formation of powders of nano order size and the average crystal size was found to be around 30–70 nm. Variation of dielectric constant and dielectric loss with frequency showed dispersion in the low frequency range and an anomaly in the temperature variation of dielectric constant is an evidence of presence of magnetoelectric coupling in the prepared nanocomposites. The magnetic behavior is found to be strongly dependent upon nickel ferrite content and annealing temperature. Magnetic field-induced relative change of the dielectric constant was observed in the nanocomposites. The fractional change of magnetic field induced in dielectric constant can also be expressed by Δε ∼ γM2 (where γ is magnetoelectric coupling coefficient)

  12. Surface properties of palladium catalysts supported on ternary ZrO2-Al2O3-WOx oxides prepared by the sol-gel method: Study of the chemical state of the support

    Science.gov (United States)

    Barrera, A.; Montoya, J. A.; del Angel, P.; Navarrete, J.; Cano, M. E.; Tzompantzi, F.; López-Gaona, A.

    2012-08-01

    The surface properties of Pd and Pd-Pt catalysts supported on binary ZrO2-WOx and ternary ZrO2-Al2O3-WOx oxides prepared by the sol-gel method were studied. Special attention was paid to the study of the texture of the catalysts as well as the chemical state of tungstated zirconia and tungstated zirconia promoted with alumina in the palladium catalysts. The catalysts were tested in the isomerization of n-hexane and were characterized by N2 physisorption, XRD, TPR, Raman spectroscopy, XPS and FT-IR of adsorbed pyridine. The catalysts had bimodal pore size distributions with mesopores in the range 55-70 Å and macropores of 1000 Å in diameter. The catalysts had a surface WOx coverage (4.4-6.0 W nm-2) lower than that of the theoretical monolayer (7.0 W nm-2). A lower acidity of the ternary ZrO2-Al2O3-WOx oxide as compared to the binary ZrO2-WOx oxide was found. Higher activity in the isomerisation of n-hexane was obtained in the Pd-Pt catalysts supported on ternary ZrAlW oxides prepared by sol-gel that is correlated with the coexistence on the surface of W4+ (WO2) or W0 and W6+ (Al2(WO4)3) species, ZrO2 in the tetragonal phase and a high amount of ZrOx suboxides species in a low oxidation state (Zr3+ and Zr2+).

  13. In vitro biocompatibility and antimicrobial activity of wet chemically prepared Ca10-xAgx(PO4)6(OH)2 (0.0 ≤ x ≤ 0.5) hydroxyapatites

    International Nuclear Information System (INIS)

    Herein, we report the effect of silver ions on the physical, antimicrobial and cytocompatibility properties of wet chemically synthesized silver doped Ca10-xAgx(PO4)6(OH)2 (0.0 ≤ x ≤ 0.5) hydroxyapatites (HAp). Silver ions containing HAp exhibit the comparable density, hardness and enhanced antimicrobial properties, in comparison to parent HAp. The optical absorption measurements confirm the presence of silver ions in the doped compositions, which are responsible for as increased antimicrobial property of doped HAp materials for x > 0.3. The cytotoxicity behavior of the doped HAp was evaluated using mouse fibroblast (L929) cell line. The important result has been that doped HAp (x > 0.3) exhibit statistically (significant) lower cell viability in comparison to undoped HAp. However, no difference in cellular functionality on doped HAp surfaces, in terms of cell adhesion and proliferation could be qualitatively observed in reference to undoped HAp. In order to explain the observed antimicrobial and cell viability properties, the in vitro release of Ag+ ions has been quantified using Inductively Coupled Plasma-Atomic Emission Spectroscopy (ICP-AES) and solubility was measured by weight loss in acetate buffer solution. - Research highlights: → Wet chemically prepared Silver doped Hydroxyapatites (HAp) showing the Comparable density and hardness in comparison to parent HAp. → 2% Silver doped HAp shows less solubility in acetate buffer in comparison to Parent HAp. → Enhanced antimicrobial property in very low concentration of silver content in Hydroxyapatite. → Silver doped HAp (x>0.3) exhibits statistically (significant) lower cell viability in comparison to parent HAp.

  14. In vitro biocompatibility and antimicrobial activity of wet chemically prepared Ca{sub 10-x}Ag{sub x}(PO{sub 4}){sub 6}(OH){sub 2} (0.0 {<=} x {<=} 0.5) hydroxyapatites

    Energy Technology Data Exchange (ETDEWEB)

    Singh, Brajendra [Department of Physics, Indian Institute of Technology Kanpur, Kanpur-208016, Uttar Pradesh (India); Dubey, Ashutosh Kumar [Department of Materials Science and Engineering, Indian Institute of Technology Kanpur, Kanpur-208016, Uttar Pradesh (India); Kumar, Samayendra [Materials Science programme, Indian Institute of Technology Kanpur, Kanpur-208016, Uttar Pradesh (India); Saha, Naresh [Department of Materials Science and Engineering, Indian Institute of Technology Kanpur, Kanpur-208016, Uttar Pradesh (India); Basu, Bikramjit, E-mail: bikram@iitk.ac.in [Department of Materials Science and Engineering, Indian Institute of Technology Kanpur, Kanpur-208016, Uttar Pradesh (India); Gupta, Rajeev [Department of Physics, Indian Institute of Technology Kanpur, Kanpur-208016, Uttar Pradesh (India); Materials Science programme, Indian Institute of Technology Kanpur, Kanpur-208016, Uttar Pradesh (India)

    2011-10-10

    Herein, we report the effect of silver ions on the physical, antimicrobial and cytocompatibility properties of wet chemically synthesized silver doped Ca{sub 10-x}Ag{sub x}(PO{sub 4}){sub 6}(OH){sub 2} (0.0 {<=} x {<=} 0.5) hydroxyapatites (HAp). Silver ions containing HAp exhibit the comparable density, hardness and enhanced antimicrobial properties, in comparison to parent HAp. The optical absorption measurements confirm the presence of silver ions in the doped compositions, which are responsible for as increased antimicrobial property of doped HAp materials for x > 0.3. The cytotoxicity behavior of the doped HAp was evaluated using mouse fibroblast (L929) cell line. The important result has been that doped HAp (x > 0.3) exhibit statistically (significant) lower cell viability in comparison to undoped HAp. However, no difference in cellular functionality on doped HAp surfaces, in terms of cell adhesion and proliferation could be qualitatively observed in reference to undoped HAp. In order to explain the observed antimicrobial and cell viability properties, the in vitro release of Ag{sup +} ions has been quantified using Inductively Coupled Plasma-Atomic Emission Spectroscopy (ICP-AES) and solubility was measured by weight loss in acetate buffer solution. - Research highlights: {yields} Wet chemically prepared Silver doped Hydroxyapatites (HAp) showing the Comparable density and hardness in comparison to parent HAp. {yields} 2% Silver doped HAp shows less solubility in acetate buffer in comparison to Parent HAp. {yields} Enhanced antimicrobial property in very low concentration of silver content in Hydroxyapatite. {yields} Silver doped HAp (x>0.3) exhibits statistically (significant) lower cell viability in comparison to parent HAp.

  15. Preparation and Chemical Compositions of Three Polysaccarides of Different Molecular Weights from Poria Cocos Wolf%三种不同分子量段茯苓多糖的制备以及其组成分析

    Institute of Scientific and Technical Information of China (English)

    黄灿; 赵骏

    2013-01-01

    Objective:Preparation and chemical compositions of three polysaccarides of different molecular weights and chemical compositions from Poria cocos Wolf were made.Methods:In this study,three polysaccharides were extracted from Poria cocos Wolf with water and sedimentation with alcohol of different concentrations.The polysacchardes were purified by sephadexG-75.Their chemical compositions were detected by TLC and GC-MS.Results:TLC and GC-MS revealed polysaccharide A was composed of mannose,glucose,galactose and fucose,and the mole ratio was 1.4 ∶ 1.17 ∶ 1∶4.21.Polysaccharide B was composed of mannose,glucose,galactose and fucose,and the mole ratio as 1 ∶ 2.36 ∶ 5.49 ∶ 2.34.Polysaccharide C was composed of mannose,glucose,galactose and fucose,and the mole ratio was 6∶81∶25 ∶ 1.Conclusion:The three polysaccharides were all composed of mannose,glucose,galactose and fucose with different mole ratios.%目的:对不同分子量段茯苓多糖进行提取、纯化以及单糖组成分析.方法:采用热水煮沸提取,三氯乙酸法除蛋白,不同浓度乙醇醇沉得到3种不同分子量段的茯苓多糖A、B、C,凝胶色谱柱纯化,样品水解经TLC及GC-MS分析确定单糖组成.结果:结果显示A由岩藻糖、甘露糖、葡萄糖、半乳糖组成,其摩尔比为:1.4∶1.17∶1∶4.21,B由岩藻糖、甘露糖、葡萄糖、半乳糖组成,其摩尔比为:1∶2.36∶5.49∶2.34,C由岩藻糖、甘露糖、葡萄糖、半乳糖组成,其摩尔比为:6∶81∶25∶1.结论:茯苓多糖A、B、C均由岩藻糖、甘露糖、葡萄糖和半乳糖以不同含量组成.

  16. Modern Chemical Technology, Volume 5.

    Science.gov (United States)

    Pecsok, Robert L., Ed.; Chapman, Kenneth, Ed.

    This volume contains chapters 26-31 for the American Chemical Society (ACS) "Modern Chemical Technology" (ChemTeC) instructional material intended to prepare chemical technologists. Chapter 26 reviews oxidation and reduction, including applications in titrations with potassium permanganate and iodometry. Coordination compounds are described in the…

  17. Preparation of americium amalgam

    International Nuclear Information System (INIS)

    Using the method of NGR-spectroscopy with the aid of 241Am isotope chemical state of transuranium elements in the volume and on the surface of amalgams is studied. Amalgam preparation was realized in a simplified electrolytic cell. It is shown that in the process of amalgam preparation the first order of reaction as to actinide is observed; americium is distributed gradually over the volume and it is partially sorbed by the surface of glass capillary. NGR spectrum of dry residue after mercury distillation at 200 deg C points to the presence of americium-mercury intermetal compounds

  18. Nanoscale Ferroelectric Switchable Polarization and Leakage Current Behavior in (Ba0.50Sr0.50(Ti0.80Sn0.20O3 Thin Films Prepared Using Chemical Solution Deposition

    Directory of Open Access Journals (Sweden)

    Venkata Sreenivas Puli

    2015-01-01

    Full Text Available Nanoscale switchable ferroelectric (Ba0.50Sr0.50(Ti0.80Sn0.20O3-BSTS polycrystalline thin films with a perovskite structure were prepared on Pt/TiOx/SiO2/Si substrate by chemical solution deposition. X-ray diffraction (XRD spectra indicate that a cubic perovskite crystalline structure and Raman spectra revealed that a tetragonal perovskite crystalline structure is present in the thin films. Sr2+ and Sn4+ cosubstituted film exhibited the lowest leakage current density. Piezoresponse Force Microscopy (PFM technique has been employed to acquire out-of-plane (OPP piezoresponse images and local piezoelectric hysteresis loop in polycrystalline BSTS films. PFM phase and amplitude images reveal nanoscale ferroelectric switching behavior at room temperature. Square patterns with dark and bright contrasts were written by local poling and reversible nature of the piezoresponse behavior was established. Local piezoelectric butterfly amplitude and phase hysteresis loops display ferroelectric nature at nanoscale level. The significance of this paper is to present ferroelectric/piezoelectric nature in present BSTS films at nanoscale level and corroborating ferroelectric behavior by utilizing Raman spectroscopy. Thus, further optimizing physical and electrical properties, BSTS films might be useful for practical applications which include nonvolatile ferroelectric memories, data-storage media, piezoelectric actuators, and electric energy storage capacitors.

  19. Chemical solution deposition preparation of double-perovskite La{sub 2}NiMnO{sub 6} film on LaAlO{sub 3} (0 0 1) substrate

    Energy Technology Data Exchange (ETDEWEB)

    Wang Tao [Anhui Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, Hefei 230031 (China); Xu Weibing [Jiangxi University of Science and Technology, Ganzhou 341000 (China); Fang Xiaodong [Anhui Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, Hefei 230031 (China)], E-mail: twang7290@ustc.edu; Dong Weiwei; Tao Ruhua; Li Da; Zhao Yiping [Anhui Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, Hefei 230031 (China); Zhu Xuebin [Key Laboratory of Materials Physics, Institute of Solid State Physics, Chinese Academy of Sciences, Hefei 230031 (China)

    2009-05-05

    The ordered double-perovskite La{sub 2}NiMnO{sub 6} films were successfully deposited on LaAlO{sub 3} substrate by chemical solution deposition method. Some La{sub 2}NiMnO{sub 6} films layer with seed layer were also prepared in order to obtain higher quality films. The X-ray diffraction and Raman scattering spectroscopy are used to characterize all the films, it is found that all films are single phase with highly (0 0 l)-oriented. The field-emission scanning electron microscopy shows that the film with seed layer is relatively smooth and dense. The magnetic measurements indicate that all films exhibit a Curie temperature of about 280 K, which is close to that of the bulk material. Moreover, the low temperature magnetization of the films with and without seed layer is different, which can be attributed to that the seed layer can prevent the diffusion between the films and the substrate.

  20. An X-band Co2+ EPR study of Zn1-xCoxO (x=0.005-0.1) nanoparticles prepared by chemical hydrolysis methods using diethylene glycol and denaturated alcohol at 5 K

    Science.gov (United States)

    Misra, Sushil K.; Andronenko, S. I.; Srinivasa Rao, S.; Chess, Jordan; Punnoose, A.

    2015-11-01

    EPR investigations on two types of dilute magnetic semiconductor (DMS) ZnO nanoparticles doped with 0.5-10% Co2+ ions, prepared by two chemical hydrolysis methods, using: (i) diethylene glycol ((CH2CH2OH)2O) (NC-rod-like samples), and (ii) denatured ethanol (CH3CH2OH) solutions (QC-spherical samples), were carried out at X-band (9.5 GHz) at 5 K. The analysis of EPR data for NC samples revealed the presence of several types of EPR lines: (i) two types, intense and weak, of high-spin Co2+ ions in the samples with Co concentration >0.5%; (ii) surface oxygen vacancies, and (iii) a ferromagnetic resonance (FMR) line. QC samples exhibit an intense FMR line and an EPR line due to high-spin Co2+ ions. FMR line is more intense, than the corresponding line exhibited by NC samples. These EPR spectra varied for sample with different doping concentrations. The magnetic states of these samples as revealed by EPR spectra, as well as the origin of ferromagnetism DMS samples are discussed.

  1. Effects of radio-frequency power on the properties of carbon thin films prepared by thermal chemical vapor deposition enhanced with remote inductively-coupled-plasma using acetylene/nitrogen mixtures

    Energy Technology Data Exchange (ETDEWEB)

    Lai, Liang-Hsun; Wu, Kuan-Chang; Shiue, Sham-Tsong, E-mail: stshiue@dragon.nchu.edu.tw

    2014-11-03

    The effects of radio-frequency (rf) power on the properties of carbon thin films prepared by thermal chemical vapor deposition (CVD) enhanced with remote inductively-coupled-plasma (ICP) are investigated. Acetylene and nitrogen were used as the precursor gases, and rf-powers of ICP were set as 0, 100, 200, 300, and 400 W. The deposition temperature, working pressure, and deposition time were set as 1248 K, 4 kPa, and 2 h, respectively. The residual gases, film thicknesses, microstructures, chemical characteristics, mechanical properties, and electrical properties of carbon thin films were investigated by residual gas analyzer (RGA), field emission scanning electron microscopy, X-ray diffractometer (and Raman scattering spectrometer), X-ray photoelectron spectrometer, nanoindenter, and four point probe, respectively. RGA results reveal that the main species in the gas phase contain H{sub 2}, C{sub 2}H, C{sub 2}H{sub 2}, HCN (or C{sub 2}H{sub 3}), and N{sub 2} (or C{sub 2}H{sub 4}). Moreover, C{sub 2}H, C{sub 2}H{sub 2}, and C{sub 2}H{sub 4} can be speculated as the main species for carbon thin film deposition. As the rf-power increases from 0 to 400 W, the deposition rate of carbon thin films decreases from 204 to 36.0 nm/h. The crystallinity and ordering degree of carbon thin films increase with increasing rf-power from 0 to 400 W, but the ratio of sp{sup 2} carbon sites in carbon thin films decreases from 95 to 75%. The Young's modulus, hardness, and electrical resistivity of carbon thin films increase with increasing rf-power. Furthermore, the effects of rf-power on the deposition rates of carbon thin films prepared by thermal CVD enhanced with remote ICP using C{sub 2}H{sub 2}/N{sub 2} and CH{sub 4}/N{sub 2} mixtures are compared. - Highlights: • Carbon films are prepared by TCVD enhanced with remote ICP using C{sub 2}H{sub 2}/N{sub 2} mixtures. • The deposition rate of carbon thin films decreases with increasing the rf-power. • C{sub 2}H, C{sub 2}H

  2. Chemical Emergencies

    Science.gov (United States)

    When a hazardous chemical has been released, it may harm people's health. Chemical releases can be unintentional, as in the case of an ... the case of a terrorist attack with a chemical weapon. Some hazardous chemicals have been developed by ...

  3. The Preparation of Graphene

    Institute of Scientific and Technical Information of China (English)

    Chen Yanyan

    2015-01-01

    Graphene has unique structure and possesses excellent physical and chemical properties, and it has received a great deal of attention in related research fields. The quality, quantity and application of graphene are related to its preparation methods. At present the bottleneck of graphene research is that both high-quality and large quantity of graphene could not be obtained simultaneously and the reason is that the basic mechanism of graphene formation has mot been wel understood.

  4. 碳酸钾化学活化法制备土霉素菌渣活性炭研究%Preparation of Oxytetracycline Bacterial Residue Activated Carbon by Chemical Activation with Potassium Carbonate

    Institute of Scientific and Technical Information of China (English)

    周保华; 高勤; 郭斌; 朱能

    2012-01-01

    为了解决制药行业土霉素菌渣处置的难题,该文以土霉素菌渣为原材料,K2CO3为活化剂,采用化学活化法制备土霉素菌渣活性炭.通过电镜扫描和氮气吸附对较佳条件下制备的活性炭特性进行了表征.实验得出制备土霉素菌渣活性炭的较佳工艺条件为:活化温度800℃,活化时间3h,活化比1∶3.该活性炭的苯酚吸附值为215 mg/g,比表面积达1 593.09 m2/g,亚甲基蓝吸附值为117 mg/g.该活性炭孔结构丰富,主要以微孔为主,平均孔径为1.09 nm,微孔孔容为0.54 cm3/g,中孔孔容为0.27 cm3/g.%In order to solve the problem of oxytetracycline bacterial residue disposal of pharmaceutical industry,the activated carbons prepared from oxytetracycline bacterial residue with K2CO3 under chemical activation are investigated here. The properties of the activated carbons under better conditions are performed by sanning electron microscopy and Nitrogen adsorption. Experimental results show that the better process conditions of preparation for oxytetracycline bacterial residue activated carbons are 800 ℃ activation temperature,3 h activation time and 1:3 activation ratio. The phenol adsorption of these activated carbons is 215 mg/g,the special surface area is 1 593. 09 m2/g and the methylene blue adsorption is 117 mg/g. The activated carbons are affluent in pores, which are mainly micropores. The average pore size of the activated carbons is 1. 09 nm, and the micropore volume and mesopore volume are 0. 54 cm3/g and 0. 27 cmVg respectively.

  5. Mechanical and thermal properties of ceramsite foamed concrete prepared with chemical foaming method%化学发泡陶粒泡沫混凝土力学及热工性能研究

    Institute of Scientific and Technical Information of China (English)

    王康; 陈国新

    2016-01-01

    In order to improve crack resistance and thermal properties of foamed concrete, hydrogen peroxide, ceramsite, glazed hollow bead, glass fiber, and cement were used to prepare glass fiber-reinforced ceramsite foamed concrete blocks with the chemical foaming method. A single factor con-trol variate method was used to test the blocks, and the effect of various factors on mechanical and thermal properties of the concrete was analyzed. An optimal mixture ratio was obtained through a multiple linear regression analysis. The splitting tensile strength of the foamed blocks was between 0. 80 MPa and 0. 90 MPa, and the compressive strength was between 7. 0 MPa and 8. 0 MPa. Re-sults show that the brittleness of foamed concrete corresponds with the increase of the hydrogen per-oxide and glazed hollow bead contents. Glass fiber can improve the splitting tensile strength and thermal performance of foamed concrete. When the hydrogen peroxide, glass fiber and glazed hollow beads are 7. 5%, 1. 0%, 8. 5% and 8. 5% of the cement mass content, respectively, the thermal conductivity of foamed concrete is 0. 203 W/( m·k) , the splitting tensile strength is 0. 81 MPa, and the compressive strength is 7. 3 MPa. Glass fiber-reinforced ceramsite foamed concrete prepared with the chemical foaming method, have high ratio of tension to compression and good thermal properties.%为改善泡沫混凝土的抗裂性能和热工性能,利用双氧水、陶粒、玻化微珠、玻璃纤维、水泥等材料,通过化学发泡法制备玻璃纤维增强型陶粒泡沫混凝土砌块,并采用单因素控制变量法进行顺序试验,分析了各因素对材料力学性能和热工性能的影响,通过多元线性回归得出满足劈拉强度在0.80~0.90 MPa、抗压强度在7.0~8.0 MPa的泡沫混凝土砌块最优配合比。结果表明:泡沫混凝土脆性随双氧水、玻化微珠和陶粒用量的增加而显著增大;玻璃纤维既可提高泡沫混凝土强度,又可改善其热

  6. Characteristics of n+ polycrystalline-Si/Al2O3/Si metal - oxide - semiconductor structures prepared by atomic layer chemical vapor deposition using Al(CH3)3 and H2O vapor

    International Nuclear Information System (INIS)

    We report interface and dielectric reliability characteristics of n+ polycrystalline-silicon (poly-Si)/Al2O3/Si metal - oxide - semiconductor (MOS) capacitors. Al2O3 films were prepared by atomic layer chemical vapor deposition using Al(CH3)3 and H2O vapor. Interface state density (Dit) and dielectric reliability properties of n+ poly-Si/Al2O3/Si MOS structures were examined by capacitance - voltage, conductance, current - voltage, and time-dependent dielectric breakdown measurements. The Dit of the n+ poly-Si/Al2O3/Si MOS system near the Si midgap is approximately 8 x 1010eV-1cm-2 as determined by the conductance method. Frequency dispersion as small as ∼20 mV and hysteresis of ∼15 mV were attained under the electric field of ±8 MV/cm. The gate leakage current of ∼36 Aa effective thickness Al2O3 dielectric measured at the gate voltage of -2.5 V is ∼-5 nA/cm2, which is approximately three orders of magnitude lower than that of a controlled oxide (SiO2). Time-dependent dielectric breakdown data of Al2O3/Si MOS capacitors under the constant current/voltage stress reveal excellent charge-to-breakdown characteristics over controlled oxide. Reliable gate oxide integrity of Al2O3 gate dielectric is manifested by the excellent distribution of gate oxide breakdown voltage on 128 million MOS capacitors having isolation edges. Extracted time constant and capture cross section of the Al2O3/Si junction are discussed. [copyright] 2001 American Institute of Physics

  7. Chemical hygiene plan

    Energy Technology Data Exchange (ETDEWEB)

    1994-09-01

    This plan was written to administer and monitor safety measures and chemical hygiene principles in the TAC Uranium Mill Tailing Remedial Action Project sample preparation facility in Albuquerque, New Mexico. It applies to toxic and/or hazardous materials to radioactive materials.

  8. Chemical hygiene plan

    International Nuclear Information System (INIS)

    This plan was written to administer and monitor safety measures and chemical hygiene principles in the TAC Uranium Mill Tailing Remedial Action Project sample preparation facility in Albuquerque, New Mexico. It applies to toxic and/or hazardous materials to radioactive materials

  9. Partial chemical characterization of antigenic preparations of chromoblastomycosis agents Caracterização química parcial de preparações antigênicas de agentes da cromoblastomicose

    Directory of Open Access Journals (Sweden)

    Tania Fraga BARROS

    1999-11-01

    Full Text Available Antigenic preparations (saline, methylic, metabolic and exoantigens of four agents of chromoblastomycosis, Fonsecaea pedrosoi, Phialophora verrucosa, Cladophialophora (Cladosporium carrionii and Rhinocladiella aquaspersa were obtained. Partial chemical characterization of these antigenic preparations was obtained by determination of the levels of total lipids, protein, and carbohydrates, and identification of the main sterols and carbohydrates. Methylic antigens presented the highest lipid contents, whereas metabolic antigens showed the highest carbohydrate content. Total lipid, protein, and carbohydrate levels were in the range of 2.33 to 2.00mg/ml, 0.04 to 0.02 mg/ml and 0.10 to 0.02 mg/ml, respectively, in the methylic antigens and in the range of 0.53 to 0.18mg/ml, 0.44 to 0.26mg/ml, and 1.82 to 1.02 mg/ml, respectively, in saline antigens. Total lipid, protein, and carbohydrate contents were in the range of 0.55 to 0.20mg/ml, 0.69 to 0.57mg/ml and 10.73 to 5.93mg/ml, respectively, in the metabolic antigens, and in the range of 0.55 to 0.15mg/ml, 0.62 to 0.20mg/ml and 3.55 to 0.42mg/ml, respectively, in the exoantigens. Phospholipids were not detected in the preparations. Saline and metabolic antigens and exoantigens presented hexose and the methylic antigen revealed additional pentose units in their composition. The UV light absorption spectra of the sterols revealed squalene and an ergosterol fraction in the antigens. The characterization of these antigenic preparations may be useful for serological evaluation of patients of chromoblastomycosis.Preparações antigênicas (antígenos salinos, metílicos, metabólicos e exoantígenos de quatro agentes da cromoblastomicose, Fonsecaea pedrosoi, Phialophora verrucosa, Cladophialophora (Cladosporium carrionii e Rhinocladiella aquaspersa foram obtidos e foi determinada a caracterização química parcial dos mesmos. Os antígenos metílicos apresentaram os maiores teores de lípides enquanto os

  10. Ternary Al{sub 2x}In{sub 2−2x}O{sub 3} films with tunable optical band gap prepared on YSZ (1 0 0) substrates by metal organic chemical vapor deposition

    Energy Technology Data Exchange (ETDEWEB)

    Feng, Xianjin; Zhao, Cansong; Li, Zhao; Luo, Yi; Ma, Jin, E-mail: jinmasduphy@163.com

    2015-07-15

    Highlights: • Ternary Al{sub 2x}In{sub 2−2x}O{sub 3} films were prepared on the YSZ (1 0 0) substrates by MOCVD at 700 °C. • The lowest resistivity of 4.84 × 10{sup −3} Ω cm was obtained for the sample with x = 0.2. • Excellent optical transparency in the UV and visible wavelength regions was achieved. • Tunable optical band gap from 3.67 to 4.73 eV was obtained. - Abstract: The ternary Al{sub 2x}In{sub 2−2x}O{sub 3} films with different Al contents of x [Al/(Al + In) atomic ratio] have been fabricated on the Y-stabilized ZrO{sub 2} (YSZ) (1 0 0) substrates by the metal organic chemical vapor deposition (MOCVD) method at 700 °C. The influence of various Al contents (x = 0.1–0.9) on the structural, electrical and optical properties of the films have been investigated. Structural analyses revealed a phase transition from the bixbyite In{sub 2}O{sub 3} structure with a single orientation along (1 0 0) to the amorphous structure as the Al content increases from 10% to 90%. The lowest resistivity of 4.84 × 10{sup −3} Ω cm with a carrier concentration of 1.1 × 10{sup 20} cm{sup −3} and a Hall mobility of 11.74 cm{sup 2} V{sup −1} s{sup −1} were obtained for the sample with x = 0.2. The average transmittances for the Al{sub 2x}In{sub 2−2x}O{sub 3} films in the visible range were all over 77% and the optical band gap of the films could be modulated from 3.67 to 4.73 eV.

  11. La{sub 1−x}Ce{sub x}Mn{sub 1−y}Co{sub y}O{sub 3} perovskite oxides: Preparation, physico-chemical properties and catalytic activity for the reduction of diesel soot

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Shaohua; Song, Chonglin, E-mail: songchonglin@tju.edu.cn; Bin, Feng; Lv, Gang; Song, Jinou; Gong, Cairong

    2014-11-14

    La{sub 1−x}Ce{sub x}Mn{sub 1−y}Co{sub y}O{sub 3} catalysts were prepared by the “glucose method”. The structures and physico-chemical properties for these catalysts were characterized using X-ray diffraction (XRD), nitrogen adsorption, scanning electron microscopy (SEM), Fourier transform infrared spectra (FT-IR), H{sub 2}-temperature-programmed reduction (H{sub 2}-TPR) and O{sub 2}-tempreature-programmed desorption (O{sub 2}-TPD). Results showed that cerium substitution at the A-site in LaMnO{sub 3} produced a CeO{sub 2} phase. The cobalt can be introduced into the B-site in La{sub 0.8}Ce{sub 0.2}MnO{sub 3} at any substitution ratio because of the similar ionic radii between cobalt and manganese. The catalytic activity for soot combustion in air was evaluated using a TG/DTA analyzer. Cerium substitution at A-site enhances the catalytic activity, while cobalt substitution at B-site inhibits the catalytic activity. The activation energy for soot combustion was calculated using the Horowitz method. The activation energy for non-catalytic soot combustion was 164.1 kJ mol{sup −1}. The addition of catalysts decreased the activation energy by about 26–63 kJ mol{sup −1}. Among the applied catalysts, Ce20Mn exhibited the lowest activation energy (101.1 kJ mol{sup −1}). - Highlights: • Cerium substitution at A-site in Mn100 enhances the catalytic activity. • Cerium substitution leads to the formation of the CeO{sub 2} phase. • Cobalt substitution at B-site in Ce20Mn generally decreases the catalytic activity. • Cerium substitution increases the α-O{sub 2} amount and low-temperature reducibility. • Cobalt substitution decreases the α-O{sub 2} amount and low-temperature reducibility.

  12. Diseño de un leudante químico bajo en sodio para preparaciones para la comunidad celíaca Designing a low-sodium chemical leavening for preparations for the celiac community

    Directory of Open Access Journals (Sweden)

    Paula Rossi

    2012-03-01

    Full Text Available Se define Enfermedad Celíaca como una intolerancia permanente a determinadas proteínas que se encuentran en el trigo, la cebada, el centeno y la avena. Las harinas no permitidas para los celíacos son más difíciles de manejar, porque no forman la red proteica de gluten que le confiere a los amasados la característica elasticidad y esponjosidad. En la mayoría de los casos se recurre a ingredientes altos en grasa y sodio. Esta situación resulta de gran importancia para la salud ya que el consumo excesivo de sodio es la principal causa de hipertensión arterial. Con el objetivo de disminuir el contenido de sodio de las preparaciones se ha desarrollado un leudante químico bajo en sodio que, junto a una disminución en el agregado de sal, ha significado un aporte sustantivo en varias recetas de panes consumidos habitualmente por esta población. Se han logrado panes saludables con características sensoriales similares a sus originales que los hacen sumamente aceptables por la población para la cual fueron diseñados.Celiac Disease is defined as a permanent intolerance to certain proteins found in wheat, barley, rye and oats. The flours that are not allowed for coeliacs are more difficult to handle, because they do not form the gluten protein network that gives the dough the characteristic elasticity and sponginess. In most cases ingredients high in fat and sodium are used. This situation is of great importance to health as the excessive consumption of sodium is the main cause of hypertension. In order to reduce the sodium content of the preparations we have developed a lowsodium chemical leavening which, together with a reduction in salt, has contributed substantially in various recipes of breads usually consumed by this population. We have obtained healthy breads with sensory characteristics similar to the original ones that make them highly acceptable in the population for which they were designed.

  13. 冻融联合优化化学法制备粗大去细胞同种异体神经%Preparing acellular nerve allografts by combined freeze-thaw and chemical methods

    Institute of Scientific and Technical Information of China (English)

    管树军; 王伟; 李岩

    2015-01-01

    thoroughly, but the basilar membrane was fuly retained. These findings indicate that the optimized combination of freeze-thaw and chemical methods can efficiently clear Schwann cels and myelin which are the major antigenic components in the peripheral nerve, while preserve the basilar membrane to promote nerve regeneration. Therefore, this method can be an ideal method for preparation of tissue engineered nerves.

  14. Imprinted photonic crystal chemical sensors

    NARCIS (Netherlands)

    Boersma, A.; Burghoorn, M.M.A.; Saalmink, M.

    2011-01-01

    In this paper we present the use of Photonic Crystals as chemical sensors. These 2D nanostructured sensors were prepared by nano-imprint lithography during which a nanostructure is transferred from a nickel template into a responsive polymer, that is be specifically tuned to interact with the chemic

  15. Graphene composites containing chemically bonded metal oxides

    Indian Academy of Sciences (India)

    K Pramoda; S Suresh; H S S Ramakrishna Matte; A Govindaraj

    2013-08-01

    Composites of graphene involving chemically bonded nano films of metal oxides have been prepared by reacting graphene containing surface oxygen functionalities with metal halide vapours followed by exposure to water vapour. The composites have been characterized by electron microscopy, atomic force microscopy and other techniques. Magnetite particles chemically bonded to graphene dispersible in various solvents have been prepared and they exhibit fairly high magnetization.

  16. PREPARATION OF HALIDES OF PLUTONIUM

    Science.gov (United States)

    Garner, C.S.; Johns, I.B.

    1958-09-01

    A dry chemical method is described for preparing plutonium halides, which consists in contacting plutonyl nitrate with dry gaseous HCl or HF at an elevated temperature. The addition to the reaction gas of a small quantity of an oxidizing gas or a reducing gas will cause formation of the tetra- or tri-halide of plutonium as desired.

  17. 21 CFR 184.1372 - Insoluble glucose isomerase enzyme preparations.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Insoluble glucose isomerase enzyme preparations... enzyme preparations. (a) Insoluble glucose isomerase enzyme preparations are used in the production of... additional requirements for enzyme preparations in the Food Chemicals Codex, 3d Ed. (1981), p. 107, which...

  18. Radioprotective preparation

    International Nuclear Information System (INIS)

    The invention is intended for radiation injuries prophylaxis in mammals. It has an well expressed radioprotective effect against acute gamma irradiation on cellular level as well as a prolonged action when applied up to 48 hours before the acute irradiation. The preparation is a coprecipitate of the natural tripeptide glutathione (reduced form) and polyvinyl pyrrolidone (pvp) in ratio 30-60/70-40. It is obtained by incubation method with subsequent lyophilization from water solution of the initial components. The molecular mass of the pvp is 20 till 360.103. 2 claims

  19. Chemical use

    Data.gov (United States)

    US Fish and Wildlife Service, Department of the Interior — This is a summary of research and activities related to chemical use on Neal Smith National Wildlife Refuge between 1992 and 2009. The chemicals used on the Refuge...

  20. Chemical and ecological health of white sucker (Catostomus commersoni) in Rock Creek Park, Washington, D.C., 2003-04 / by Cherie V. Miller ... [et al.] ; prepared in copoeration with the National Park Service

    OpenAIRE

    Miller, Cherie V.; Weyers, Holly S.; Blazer, Vicki S.; Freeman, Mary E.

    2009-01-01

    Several classes of chemicals that are known or suspected contaminants were found in bed sediment in Rock Creek, including polyaromatic hydrocarbons (PAHs), phthalate esters, organochlorine pesticides, dioxins and furans, trace metals and metalloids (mercury, arsenic, cadmium, chromium, cobalt, copper, lead, nickel, silver, and zinc), and polychlorinated biphenyls (total PCBs and selected aroclors). Concentrations of many of these chemicals consistently exceeded thresholdor chronic-effects gui...

  1. Chemical sensor

    Science.gov (United States)

    Rauh, R. David (Inventor)

    1990-01-01

    A sensor for detecting a chemical substance includes an insertion element having a structure which enables insertion of the chemical substance with a resulting change in the bulk electrical characteristics of the insertion element under conditions sufficient to permit effective insertion; the change in the bulk electrical characteristics of the insertion element is detected as an indication of the presence of the chemical substance.

  2. Chemical machining

    Directory of Open Access Journals (Sweden)

    A. Yardimeden

    2007-08-01

    Full Text Available Purpose: Nontraditional machining processes are widely used to manufacture geometrically complex and precision parts for aerospace, electronics and automotive industries. There are different geometrically designed parts, such as deep internal cavities, miniaturized microelectronics and fine quality components may only be produced by nontraditional machining processes. This paper is aiming to give details of chemical machining process, industrial applications, applied chemical etchants and machined materials. Advantages and disadvantages of the chemical machining are mentioned.Design/methodology/approach: In this study, chemical machining process was described its importance as nontraditional machining process. The steps of process were discussed in detail. The tolerances of machined parts were examined.Findings: Paper describes the chemical machining process, industrial applications, applied chemical etchants and machined materials.Practical implications: The machining operation should be carried out carefully to produce a desired geometry. Environmental laws have important effects when chemical machining is used.Originality/value: The importance of nontraditional machining processes is very high.

  3. Chemical Leukoderma.

    Science.gov (United States)

    Bonamonte, Domenico; Vestita, Michelangelo; Romita, Paolo; Filoni, Angela; Foti, Caterina; Angelini, Gianni

    2016-01-01

    Chemical leukoderma, often clinically mimicking idiopathic vitiligo and other congenital and acquired hypopigmentation, is an acquired form of cutaneous pigment loss caused by exposure to a variety of chemicals that act through selective melanocytotoxicity. Most of these chemicals are phenols and aromatic or aliphatic catechols derivatives. These chemicals, however, are harmful for melanocytes in individuals with an individual susceptibility. Nowadays, chemical leukoderma is fairly common, caused by common domestic products. The presence of numerous acquired confetti- or pea-sized macules is clinically characteristic of chemical leukoderma, albeit not diagnostic. Other relevant diagnostic elements are a history of repeated exposure to a known or suspected depigmenting agent at the sites of onset and a macules distribution corresponding to sites of chemical exposure. Spontaneous repigmentation has been reported when the causative agent is avoided; the repigmentation process is perifollicular and gradual, taking place for a variable period of weeks to months. PMID:27172302

  4. 批量制备Fe2O3/Al2O3氧载体及褐煤化学链燃烧实验研究%Batch Preparation of Fe2O3/Al2O3 Oxygen Carriers for Chemical Looping Combustion of Lignite

    Institute of Scientific and Technical Information of China (English)

    郭磊; 赵海波; 马琎晨; 梅道锋; 方彦飞; 郑楚光

    2013-01-01

    Freeze granulation,spray drying,impregnation and mechanical mixing methods were adopted to prepare Fe2O3/Al2O3 oxygen carriers.To identify the appropriate technologies for batch preparation of the oxygen carriers,the four preparation methods were compared in terms of yield rate,preparation period,physical and chemical characteristics and performance in chemical looping combustion (CLC) of lignite.The experimental results show that freeze granulation has the highest yield rate of carrier with the best mechanical strength.CLC tests of lignite demonstrate that the oxygen carriers prepared by freeze granulation and spray drying bring the highest carbon conversion rate,followed by impregnation and mechanical mixing; and the oxygen carriers prepared by the first two methods have higher chemical reactivity and more stable performance.In the four reduction processes with oxygen carriers prepared by all the four preparation methods,CO2 capture efficiencies exceed 88%; the yield rate of CO2 increases with the rate of carbon conversion,finally approaching 100%; and the combustion efficiencies are above 90%.These indicate that the oxygen carriers prepared by the four methods all have good performances for CO2 capture and high utilization degree of the combustible components.Freeze granulation and spray drying methods can be considered preferentially for batch preparation of oxygen carriers for the CLC of lignite.%采用冷冻成粒法、喷雾干燥法、浸渍法、机械混合法批量制备了Fe2O3/Al2O3氧载体,从氧载体产率、制备周期、物理化学表征、煤化学链燃烧中氧载体性能等角度比较各种批量制备方法,确定合适的批量制备技术.实验结果表明,冷冻成粒法的氧载体产率较高,机械性能最优;与褐煤的化学链燃烧实验中,喷雾干燥法和冷冻成粒法制备的氧载体导致碳转化速率较快,然后依次为浸渍法和机械混合法;且前两种方法制备的氧载体的循环稳定性

  5. Chemical Synthesis of Copper Nanoparticles

    Directory of Open Access Journals (Sweden)

    Hamid Reza Ghorbani

    2014-06-01

    Full Text Available Metal nanoparticles have attracted considerable interest particularly because of the size dependence of physical and chemical properties and its enormous technological potential. Among different metal nanoparticles, copper nanoparticles have attracted great attention because copper is one of the most key metals in new technology. Chemical methods are used to synthesize copper nanoparticles and among them chemical reduction is the most frequently applied method for the preparation of stable, colloidal dispersions in organic solvents. In this paper, a brief overview of the current research worldwide in the chemical synthesis of copper nanoparticles is discussed.

  6. Chemical networks*

    OpenAIRE

    Thi Wing-Fai

    2015-01-01

    This chapter discusses the fundamental ideas of how chemical networks are build, their strengths and limitations. The chemical reactions that occur in disks combine the cold phase reactions used to model cold molecular clouds with the hot chemistry applied to planetary atmosphere models. With a general understanding of the different types of reactions that can occur, one can proceed in building a network of chemical reactions and use it to explain the abundance of species seen in disks. One o...

  7. AFFINITY OF LIGNIN PREPARATIONS TOWARDS GENOTOXIC COMPOUNDS

    Directory of Open Access Journals (Sweden)

    Božena Košíková

    2009-02-01

    Full Text Available The carcinogenicity and mutagenicity of chemicals may be modulated by other chemicals, including those prepared by organic synthesis. Consid-ering the several drawbacks of synthetic compounds vis-a-vis the human organism, the lignin biomass component was examined for this purpose. The binding affinity of lignin samples prepared by chemical and biological modification of lignin products derived from chemical wood treatment towards for N-nitrosodiethylamine (NDA was examined. The protective role of the lignin samples against carcinogenesis was tested on a well-known model carcinogen, N-methyl-N´-nitro-N-nitrosoguanidine (MNNG. The observed ability of a series of lignin preparations to reduce alkylation damage of deoxyribonucleic acid (DNA on hamster cells in vitro could be explained by their affinity to bind N-nitrosoamines. The results indicate that lignin has potential to protect living organisms against damaging effects of different genotoxicants.

  8. Chemical machining

    OpenAIRE

    A. Yardimeden; T. Ozben; O. Cakir

    2007-01-01

    Purpose: Nontraditional machining processes are widely used to manufacture geometrically complex and precision parts for aerospace, electronics and automotive industries. There are different geometrically designed parts, such as deep internal cavities, miniaturized microelectronics and fine quality components may only be produced by nontraditional machining processes. This paper is aiming to give details of chemical machining process, industrial applications, applied chemical etchants and mac...

  9. Chemical Radioprotectors

    Directory of Open Access Journals (Sweden)

    S. N. Upadhyay

    2005-10-01

    Full Text Available Protection of biological systems against radiation damage is of paramount importance during accidental and unavoidable exposure to radiation. Several physico-chemical and biological factors collectively contribute to the damage caused by radiation and are, therefore, targets for developing radioprotectors. Work on the development of chemicals capable of protecting biological systemsfrom radiation damage was initiated nearly six decades ago with cysteine being the first molecule to be reported. Chemicals capable of scavenging free radicals, inducing oxygen depletion,antioxidants and modulators of immune response have been some of the radioprotectors extensively investigated with limited success. Mechanism of action of some chemical radioprotectors and their combinations have been elucidated, while further understanding is required in many instances. The present review elaborates on structure-activity relationship of some of the chemical radioprotectors, their evaluation, and assessment, limitation, and future prospects.

  10. Physical-Chemical Characterization of Nanodispersed Powders Produced by a Plasma-Chemical Technique

    Institute of Scientific and Technical Information of China (English)

    M. GEORGIEVA; G. VISSOKOV; Iv. GRANCHAROV

    2007-01-01

    This article presents a review on the physical-chemical properties and characteristics of plasma-chemically produced nanodispersed powders (NDP), such as metals, oxides, nitrides, carbides, and catalysts. The plasma-chemical preparation of the powders was carried out in thermal plasma (TP) created by means of high-current electric arcs, plasma jets, high-frequency (HF) discharges, etc. We also discuss certain properties and characteristics of the NDPs, which are determined largely by the conditions of preparation.

  11. Biological and Chemical Security

    Energy Technology Data Exchange (ETDEWEB)

    Fitch, P J

    2002-12-19

    The LLNL Chemical & Biological National Security Program (CBNP) provides science, technology and integrated systems for chemical and biological security. Our approach is to develop and field advanced strategies that dramatically improve the nation's capabilities to prevent, prepare for, detect, and respond to terrorist use of chemical or biological weapons. Recent events show the importance of civilian defense against terrorism. The 1995 nerve gas attack in Tokyo's subway served to catalyze and focus the early LLNL program on civilian counter terrorism. In the same year, LLNL began CBNP using Laboratory-Directed R&D investments and a focus on biodetection. The Nunn-Lugar-Domenici Defense Against Weapons of Mass Destruction Act, passed in 1996, initiated a number of U.S. nonproliferation and counter-terrorism programs including the DOE (now NNSA) Chemical and Biological Nonproliferation Program (also known as CBNP). In 2002, the Department of Homeland Security was formed. The NNSA CBNP and many of the LLNL CBNP activities are being transferred as the new Department becomes operational. LLNL has a long history in national security including nonproliferation of weapons of mass destruction. In biology, LLNL had a key role in starting and implementing the Human Genome Project and, more recently, the Microbial Genome Program. LLNL has over 1,000 scientists and engineers with relevant expertise in biology, chemistry, decontamination, instrumentation, microtechnologies, atmospheric modeling, and field experimentation. Over 150 LLNL scientists and engineers work full time on chemical and biological national security projects.

  12. Hazardous Chemicals

    Centers for Disease Control (CDC) Podcasts

    2007-04-10

    Chemicals are a part of our daily lives, providing many products and modern conveniences. With more than three decades of experience, The Centers for Disease Control and Prevention (CDC) has been in the forefront of efforts to protect and assess people's exposure to environmental and hazardous chemicals. This report provides information about hazardous chemicals and useful tips on how to protect you and your family from harmful exposure.  Created: 4/10/2007 by CDC National Center for Environmental Health.   Date Released: 4/13/2007.

  13. Effect of deposition variables on properties of CBD ZnS thin films prepared in chemical bath of ZnSO{sub 4}/SC(NH{sub 2}){sub 2}/Na{sub 3}C{sub 3}H{sub 5}O{sub 7}/NH{sub 4}OH

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Wei-Long [Department of Materials Science and Engineering, National Formosa University, 64, Wunhua Road, Huwei, Yunlin, 632, Taiwan (China); Yang, Chang-Siao [Graduate School of Materials Science, National Yunlin University of Science and Technology, 123 University Road, Section 3, Douliou, Yunlin, 64002, Taiwan (China); Hsieh, Shu-Huei [Department of Materials Science and Engineering, National Formosa University, 64, Wunhua Road, Huwei, Yunlin, 632, Taiwan (China); Chen, Wen-Jauh, E-mail: chenwjau@yuntech.edu.tw [Graduate School of Materials Science, National Yunlin University of Science and Technology, 123 University Road, Section 3, Douliou, Yunlin, 64002, Taiwan (China); Fern, Chi-Lon [Graduate School of Materials Science, National Yunlin University of Science and Technology, 123 University Road, Section 3, Douliou, Yunlin, 64002, Taiwan (China)

    2013-01-01

    Highlights: Black-Right-Pointing-Pointer The CBD ZnS thin films were prepared on soda lime glass in a bath of ZnSO{sub 4}/SC(NH{sub 2}){sub 2}/Na{sub 3}C{sub 3}H{sub 5}O{sub 7}/NH{sub 4}OH. Black-Right-Pointing-Pointer The transmittance for ultraviolet-visible rays (300-800 nm) through those films is in a range of 70.8-87.8%. Black-Right-Pointing-Pointer The ZnS thin films have an energy gap from 3.885 to 3.980 eV which increases with the decrease of ZnSO{sub 4} concentration. Black-Right-Pointing-Pointer The CBD ZnS thin film with a Zn/S of 1:1 could be prepared at 80 Degree-Sign C in chemical bath. - Abstract: The CBD ZnS thin films were prepared on substrates of soda lime glass in chemical bath. The effect of deposition variables including zinc sulfate, thiourea, tri-sodium citrate, ammoina water, bath temperature, and deposition time on the properties of CBD ZnS thin films were comprehensively studied. The CBD ZnS thin films were characterized by a field emission scanning electron microscope (FESEM) for the surface and cross section morphologies and thicknesses, an energy dispersive spectrometer equipped in FESEM for the atomic% of Zn and S, an ultraviolet-visible spectrometer (300-800 nm) for the transmittance and energy gap, and an atomic force microscope for the surface roughness. The results showed that the CBD ZnS thin films have a transmittance for ultraviolet-visible rays (300-800 nm) from 70.8 to 87.8%. The CBD ZnS thin films prepared in bath 5 have an energy gap from 3.881 to 3.980 eV. The CBD ZnS thin films prepared in bath 6 have a growth rate from 1.8 to 3.2 nm/min and activation energy of 59.8 kJ/mol for their growth.

  14. A Comparison between Chemical Synthesis Magnetite Nanoparticles and Biosynthesis Magnetite

    OpenAIRE

    Seyed Abolghasem Kahani; Zahra Yagini

    2014-01-01

    The preparation of Fe3O4 from ferrous salt by air in alkaline aqueous solution at various temperatures was proposed. The synthetic magnetites have different particle size distributions. We studied the properties of the magnetite prepared by chemical methods compared with magnetotactic bacterial nanoparticles. The results show that crystallite size, morphology, and particle size distribution of chemically prepared magnetite at 293 K are similar to biosynthesis of magnetite. The new preparation...

  15. PREPARATION OF ACTIVATED CARBON FROM PALM OIL SHELL BY CHEMICAL ACTIVATION WITH Na2CO3 AND ZnCl2 AS IMPRENATED AGENTS FOR H2S ADSORPTION

    Directory of Open Access Journals (Sweden)

    Kanokorn Hussaro

    2014-01-01

    Full Text Available Hydrogen Sulfide (H2S, rotten-egg is one of the major environmental pollutants having its sources in natural and anthropogenic activities. It’s had smell gas produced by anaerobic digestion in acid condition from organic and inorganic compounds containing sulphur, presents dual problems of its toxicity and foul ordour. One of methods of its removal is adsorption. Activated carbon is a widely used adsorbent in the treatment of air pollution. Adsorption type and capacity are primarily based on the physical properties of pores, namely the surface area. Convetionnally, activated carbon is produced from biomass residues, wood coal and agricultural residuces. Today, one promising approach for the production of cheap and efficient activated carbon is used of waste from palm oil mill industries, which is palm oil shell. Palm oil shell is available in large quantities of approximately 0.53 million tonnes annually in Thailand. Palm oil shell is a by-products of the palm oil industry and was used as a raw material in this study due to its high carbon content, high density and low ash content. Normally, H2S in biogas, which is found the range between as low as about 50-10,000 ppm depending on the feed material composition to prodction, can cause corrosion to engine and metal substance via of SO2 from combustion. H2S must be removed from biogas product prior to further utilization. Therefore, in these research the usage of palm oil shell is especially important due to its high value added for produced activated carbon adsorbent for H2S adsorption in biogas product. In this study, fixed bed reactor (stainless steel with 54.1 mm internal diameter and 320 mm length was studied to observe the effect of char product: Chemical agent ratio (Na2CO3 and ZnCl2, 1:1 to 1:3, which there are activated at 700°C activation temperature for 2 h on the chemical and physical properties

  16. Spectroscopic ellipsometry characterization of nano-crystalline diamondfilms prepared at various substrate temperatures and pulsed plasma frequencies using microwave plasma enhanced chemical vapor deposition apparatus with linear antenna delivery

    Czech Academy of Sciences Publication Activity Database

    Mistrík, J.; Janíček, P.; Taylor, Andrew; Fendrych, František; Fekete, Ladislav; Jäger, Aleš; Nesládek, M.

    2014-01-01

    Roč. 571, č. 1 (2014), s. 230-237. ISSN 0040-6090 R&D Projects: GA ČR GA13-31783S; GA MŠk(CZ) LM2011026 Grant ostatní: COST Nano TP(XE) MP0901; OP VK(XE) CZ.1.07/2.3.00/20.0306 Institutional support: RVO:68378271 Keywords : nanocrystalline diamond * thin films * microwave plasma-enhanced chemical vapor deposition * pulsed plasma * low deposition temperature Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 1.759, year: 2014

  17. Chemical Peels

    Science.gov (United States)

    ... pills, who subsequently become pregnant or have a history of brownish facial discoloration. Scarring Reactivation of cold sores What can I expect after having a chemical peel? All peels require some follow-up care: ...

  18. Unnecessary Chemicals

    Science.gov (United States)

    Johnson, Anita

    1978-01-01

    Discusses the health hazards resulting from chemical additions of many common products such as cough syrups, food dyes, and cosmetics. Steps being taken to protect consumers from these health hazards are included. (MDR)

  19. Chemical kinetics

    International Nuclear Information System (INIS)

    This book gives descriptions of chemical kinetics. It starts summary of chemical kinetics and reaction mechanism, and explains basic velocity law, experiment method for determination of reaction velocity, temperature dependence of reaction velocity, theory of reaction velocity, theory on reaction of unimolecular, process of atom and free radical, reaction in solution, catalysis, photochemical reaction, such as experiment and photochemical law and rapid reaction like flame, beam of molecule and shock tube.

  20. The research and preparation of an instant chemical deoxidizer—HCY and its%工业锅炉HCY速效化学除氧剂及加药器的研制

    Institute of Scientific and Technical Information of China (English)

    马铭杰; 王德林

    2001-01-01

    A new kind of instant chemical deoxidizer and its doser for industrial low-pressure boiler and heating network system have been made,which can improve chemical reaction speed of deoxidization under the condition of the water supplied in normal temperature,and make the water reach the state without dissolved oxygen before entering the boiler. The doser whose structure is simple and easy to manage can complete a course of feeding continuously,automatically,uniformly and quantitatively.%研制了一种速效化学除氧剂及新型加药器,用于工业低压锅炉及热网系统,能够提高锅炉常温给水情况下的除氧化学反应速度,使给水在进锅炉前即达到无氧状况;加药器结构简单,管理方便,可实现连续自动均匀定量的加药过程。

  1. Recommended Inorganic Chemicals for Calibration.

    Science.gov (United States)

    Moody, John R.; And Others

    1988-01-01

    All analytical techniques depend on the use of calibration chemicals to relate analyte concentration to instrumental parameters. Discusses the preparation of standard solutions and provides a critical evaluation of available materials. Lists elements by group and discusses the purity and uses of each. (MVL)

  2. Preparação e caracterização de carvão ativado quimicamente a partir da casca de arroz Preparation and characterization of chemically activated carbon from rice hulls

    Directory of Open Access Journals (Sweden)

    Miguel A. Schettino Jr.

    2007-01-01

    Full Text Available This work consists in a study about the chemical activation of charred rice hulls using NaOH as the activation agent. The influence of the naturally-occurring silica was particularly evidenced. X-ray diffraction patterns showed the formation of sodium carbonate and silicates in the activated samples, whereas thermogravimetric curves revealed a strong reduction in the ash content of these samples after washing with water. Nitrogen adsorption data indicated a microporosity development only in the washed samples, with BET surface area values of 450 and 1380 m²/g achieved for the samples activated at 800 °C starting from the precursor with or without silica, respectively.

  3. Chemical networks

    Science.gov (United States)

    Thi, Wing-Fai

    2015-09-01

    This chapter discusses the fundamental ideas of how chemical networks are build, their strengths and limitations. The chemical reactions that occur in disks combine the cold phase reactions used to model cold molecular clouds with the hot chemistry applied to planetary atmosphere models. With a general understanding of the different types of reactions that can occur, one can proceed in building a network of chemical reactions and use it to explain the abundance of species seen in disks. One on-going research subject is finding new paths to synthesize species either in the gas-phase or on grain surfaces. Specific formation routes for water or carbon monoxide are discussed in more details. 13th Lecture of the Summer School "Protoplanetary Disks: Theory and Modelling Meet Observations"

  4. Characterization of photoluminescent (Y{sub 1{minus}x}Eu{sub x}){sub 2}O{sub 3} thin-films prepared by metallorganic chemical vapor deposition

    Energy Technology Data Exchange (ETDEWEB)

    McKittrick, J.; Bacalski, C.F.; Hirata, G.A. [Univ. of California, San Diego, La Jolla, CA (United States); Hubbard, K.M.; Pattillo, S.G.; Salazar, K.V.; Trkula, M. [Los Alamos National Lab., NM (United States). Materials Science and Technology Div.

    1998-12-01

    Europium doped yttrium oxide, (Y{sub 1{minus}x}Eu{sub x}){sub 2}O{sub 3}, thin-films were deposited on silicon and sapphire substrates by metallorganic chemical vapor deposition (MOCVD). The films were grown in a MOCVD chamber reacting yttrium and europium tris(2,2,6,6-tetramethyl-3,5,-heptanedionates) precursors in an oxygen atmosphere at low pressures (5 Torr) and low substrate temperatures (500--700 C). The films deposited at 500 C were flat and composed of nanocrystalline regions of cubic Y{sub 2}O{sub 3}, grown in a textured [100] or [110] orientation to the substrate surface. Films deposited at 600 C developed from the flat, nanocrystalline morphology into a plate-like growth morphology oriented in the [111] with increasing deposition time. Monoclinic Y{sub 2}O{sub 3}:Eu{sup 3+} was observed in x-ray diffraction for deposition temperatures {ge}600 C on both (111) Si and (001) sapphire substrates. This was also confirmed by the photoluminescent emission spectra.

  5. Spectroscopic ellipsometry characterization of nano-crystalline diamond films prepared at various substrate temperatures and pulsed plasma frequencies using microwave plasma enhanced chemical vapor deposition apparatus with linear antenna delivery

    Energy Technology Data Exchange (ETDEWEB)

    Mistrik, J., E-mail: jan.mistrik@upce.cz [Institute of Applied Physics and Mathematics, University of Pardubice, Studentska 95, 53210 Pardubice (Czech Republic); Janicek, P. [Institute of Applied Physics and Mathematics, University of Pardubice, Studentska 95, 53210 Pardubice (Czech Republic); Taylor, A.; Fendrych, F.; Fekete, L.; Jager, A. [Institute of Physics, Academy of Sciences of the Czech Republic, v.v.i., Prague 8 (Czech Republic); Nesladek, M. [IMOMEC Division, IMEC, Institute for Materials Research, University Hasselt, Wetenschapspark 1, B3590 (Belgium)

    2014-11-28

    A series of nanocrystalline diamond (NCD) films were deposited by a custom made microwave plasma enhanced chemical vapor deposition apparatus with linear antenna delivery at different substrate temperatures (520–600 °C) and pulsed plasma frequencies (2.7–14.3 kHz) in a hydrogen rich working gas mixture of H{sub 2}/CH{sub 4}/CO{sub 2}. Films were deposited onto naturally oxidized Si wafers pre-seeded with nanodiamond particles. Spectro-ellipsometry characterization of the NCD films was carried out considering various model structures (single and bi-layer models) and various NCD optical constant parameterizations (Tauc–Lorentz and effective medium approximation with different non-diamond component representations). It has been shown that substrate temperature can be lowered with a simultaneous increase in pulsed plasma frequency while still providing high quality NCD films with non-diamond component fraction in the bulk layer of about 5% (identically estimated by ellipsometry and Raman spectroscopy). Films' thickness and their surface roughness were found consistent with atomic force and secondary electron microscopies. Among various NCD structure models the most appropriate has been selected. - Highlights: • Assessment of most appropriate model structure for nano-crystalline diamond (NCD) films • Interrelation between deposition conditions and diamond quality of NCD films • Identification of non-diamond component in NCD films • Comparison of results obtained by ellipsometry and Raman spectroscopies.

  6. Obtenção e caracterização de materiais argilosos quimicamente ativados para utilização em catálise Preparation and characterization of chemically activated clays for use in catalysis

    Directory of Open Access Journals (Sweden)

    M. G. F. Rodrigues

    2006-12-01

    Full Text Available O principal objetivo deste trabalho é caracterizar argilas esmectíticas "Chocolate" de Boa-Vista, PB, tanto na sua forma natural quanto tratada quimicamente, visando sua aplicação em catálise. As argilas foram caracterizadas por fluorescência de raios X, difração de raios X e espectrofotometria de absorção óptica na região do infravermelho. Os resultados mostraram que o tratamento ácido alterou a estrutura da montmorilonita. A reação de isomerização do meta-xileno, para o material ativado, mostrou que a argila ácida foi mais ativa que a natural.The main objective of this paper is to characterize the chocolate smectite clays of Boa-Vista, PB, Brazil, in their natural form, and after chemical treatment, for their application in catalysis. The experimental methods were: X-ray fluorescence, X-ray diffraction and infrared spectroscopy. The results show that the acid treatment altered the montimorillonite structure. The obtained reaction (isomerization of m-xylene for the treated material showed that treated clays were more active than the natural ones.

  7. Chemical pressure

    OpenAIRE

    Hauser, Andreas; Amstutz, Nahid; Delahaye, Sandra; Sadki, Asmaâ; Schenker, Sabine; Sieber, Regula; Zerara, Mohamed

    2002-01-01

    The physical and photophysical properties of three classic transition metal complexes, namely [Fe(bpy)3]2+, [Ru(bpy)3]2+, and [Co(bpy)3]2+, can be tuned by doping them into a variety of inert crystalline host lattices. The underlying guest-host interactions are discussed in terms of a chemical pressure.

  8. Chemical Peels

    Science.gov (United States)

    ... resources Meet our partners Español Donate Diseases and treatments Acne and rosacea Bumps and growths Color problems Contagious skin diseases ... Chemical peels public SPOT Skin Cancer™ Diseases and treatments Acne and rosacea Bumps and growths Color problems Contagious skin diseases ...

  9. Chemical Mahjong

    Science.gov (United States)

    Cossairt, Travis J.; Grubbs, W. Tandy

    2011-01-01

    An open-access, Web-based mnemonic game is described whereby introductory chemistry knowledge is tested using mahjong solitaire game play. Several tile sets and board layouts are included that are themed upon different chemical topics. Introductory tile sets can be selected that prompt the player to match element names to symbols and metric…

  10. Chemical dispersants

    NARCIS (Netherlands)

    Rahsepar, Shokouhalsadat; Smit, Martijn P.J.; Murk, Albertinka J.; Rijnaarts, Huub H.M.; Langenhoff, Alette A.M.

    2016-01-01

    Chemical dispersants were used in response to the Deepwater Horizon oil spill in the Gulf of Mexico, both at the sea surface and the wellhead. Their effect on oil biodegradation is unclear, as studies showed both inhibition and enhancement. This study addresses the effect of Corexit on oil biodeg

  11. 紫菜多糖Fe(Ⅲ)配合物的制备及其理化性质%STUDY ON PREPARATION AND CHEMICAL CHARACTERIZATION OF IRON(Ⅲ)—PORPHYRA POLYSACCHARIDE COMPLEX

    Institute of Scientific and Technical Information of China (English)

    孟凡德; 赵全芹; 刘学启; 李明霞; 刘洛生

    2001-01-01

    目的:从紫菜中提取多糖,然后与Fe(Ⅲ)合成一种新型的营养补铁剂。方法:合成紫菜多糖Fe(Ⅲ)配合物(PTC),并测定其相应的理化性质。结果:PTC的水溶液中不存在游离的Fe(Ⅲ),表明Fe(Ⅲ)与紫菜多糖形成了稳定的配合物。PTC在pH 7.34的生理盐水中不沉、不水解;动力学实验表明PTC中的Fe(Ⅲ)易被还原。经红外光谱分析,PTC是以β-(FeOOH)n为微核,紫菜多糖在核表面形成化合物。结论:PTC有望成为较好生物利用度的营养型补铁剂。%OBJECTIVE:Porphyra polysaccharide isolated from Porphyra,then iron(Ⅲ)-porphyra polysaccharide(PTC)complex was synthesized with FeCl3 and porphyra polysaccharied.METHODS:A new kind of iron-supplementary drug has been prepared.RESULTS:Experiment showed that porphyra polysaccharied iron(Ⅲ)complex was able to be dissolve in water and its solution assumed neutral,and this complex has no precipitate at pH to 11,therefore,this complex was very stable.The investigation by infrared spectra indicated that the structure of porphyra polysaccharide iron(Ⅲ)had been an interfacial complex with β-(FeOOH)ncore.Because this complex was not precipitated and dissociated at the physiological pH=7.34.CONCLUSION:Porphyra polysaccharide iron(Ⅲ) complex was able to become higher bioavailability and nutrition iron-supplementary.

  12. Career Opportunities in Chemistry and Chemical Engineering.

    Science.gov (United States)

    Glover, Trienne

    This pamphlet discusses career and employment opportunities in chemical engineering. Necessary college preparation is described and median salaries by degree are tabulated. Nontraditional careers in chemistry are also described. Future demand for chemists and chemical engineers is projected to 1985 and the availability of jobs for women and…

  13. Controle químico de arroz vermelho no sistema de preparo do solo por inundação em Santa Catarina Chemical control of red rice for the submerged soil preparation system, in Santa Catarina

    Directory of Open Access Journals (Sweden)

    M.G. Ramos

    1982-06-01

    Full Text Available Este trabalho foi desenvolvido para se encontrar um método de controle químico do arroz. Os experimentos foram realizados na Região do Baixo Vale do Itajaí, nos anos de 1978 e 1980. Os herbicidas 2,4-D amina, benthiocarb, oxadiazon, metolachlor e alachlor, quando aplicados em quadros inundados e, com 13 e 15 dias de antecedência à semeadura do aroz cultivado, apresentaram controle de arroz vermelho acima de 75% e controle total das plantas daninhas comuns da área. A população do arroz cultivado não foi afetada com a aplicação desses herbicidas. As produções alcançadas, com a aplicação desses herbicidas foi variável e dependia do nível de infestação de arroz vermelho e das outras plantas daninhas.To study the efficiency of the chemical method for red rice control three field experi ments were carried out at Low Itajai Valley in the years 1978 and 1980. The herbicides 2,4-D amine, benthiocarb, oxadiazon, metolachlor, and alachlor were applied on submerged fields, 13 to 15 days before the seeding of the cultivated rice. The control cf red rice was over 75 % and total for the other common weeds with the herbicides. None of the herbicides caused any damage to the cultivated rice. The yields for rice were depending on the level of red rice and other weeds infestation.

  14. Optical properties and chemical composition analyses of mixed rare earth oxyorthosilicate (R2SiO5, R=La, Gd and Y) doped Dy3+ phosphors prepared by urea-assisted solution combustion method

    Science.gov (United States)

    Ogugua, S. N.; Shaat, S. K. K.; Swart, H. C.; Ntwaeaborwa, O. M.

    2015-08-01

    Dysprosium (Dy3+) doped lanthanum gadolinium oxyorthosilicate (LaGdSiO5), lanthanum yttrium oxyorthosilicate (LaYSiO5) and gadolinium yttrium oxyorthosilicate (GdYSiO5) phosphors (in powder form) were synthesized by urea-assisted combustion method. The X-ray diffractometer analysis confirmed that the LaGdSiO5, LaYSiO5 and GdYSiO5 crystalized in monoclinic phases. The chemical composition of the phosphors was analyzed by measuring the atomic and molecular ionic species using the time of flight secondary ion mass spectroscopy (ToF SIMS). In addition, ToF SIMS imaging technique was used to determine the distribution of the Dy3+ dopant ions on the surface on the phosphors. The average crystallite sizes and lattice strains of the phosphor were increased by Dy3+ doping. The field emission scanning electron microscope images showed that the powders were made up of an agglomeration of particles with no regular shape. The photoluminescence data showed narrow line emission peaks at the wavelengths of 485 nm (minor emission) and 573 nm (major emission) associated with the f→f transitions of Dy3+. The photoluminescence (PL) measurements showed that the emission peak of LaGdSiO5:Dy3+ was ~3× more intense than those of LaYSiO5:Dy3+ and GdYSiO5:Dy3+ when excited using monochromatic xenon lamp with a wavelength of 241 nm. However, when the powders were excited using a 325 nm He-Cd laser, the highest PL emission intensity was observed from GdYSiO5:Dy3+.

  15. Rare earths: preparation of spectro chemically pure standards, study of their carbonates and synthesis of a new compound series - the peroxy carbonates; Terras-raras: obtencao de padroes espectroquimicos, estudo dos carbonatos e sintese dos peroxicarbonatos. Uma nova serie de compostos

    Energy Technology Data Exchange (ETDEWEB)

    Queiroz, Carlos Alberto da Silva

    1996-05-01

    In this work the following studies are concerned: I) preparation of lanthanum, cerium, praseodymium, neodymium and samarium oxides for use as spectro chemically pure standards; II) behavior of the rare earth (La, Ce, Pr, Nd, Sm) carbonates soluble in ammonium carbonate and mixture of ammonium carbonate/ammonium hydroxide, and III) synthesis and characterization of rare earth peroxy carbonates - a new series of compounds. Data for the synthesis and characterization of the rare earths peroxy carbonates described for the first time in this work are presented and discussed. With the aid of thermal analysis (TG-DTG) the thermal stability and the stoichiometric composition for new compounds were established and a mechanism of thermal decomposition was proposed. The peroxy carbonate was prepared by the addition of hydrogen peroxyde to the complexed soluble rare earths carbonates. These studies included also the determinations of active oxygen, the total rare earth oxide by gravimetry and complexometry and the C, H and N contents by microanalysis. The new compounds were also investigated by infrared spectroscopy. (author)

  16. Synthesis, characterization and study of magnetic, electrical and dielectric properties of La{sub 1−x}Dy{sub x}Co{sub 1−y}Fe{sub y}O{sub 3} nanoparticles prepared by wet chemical route

    Energy Technology Data Exchange (ETDEWEB)

    Choudhry, Qurshia [Department of Chemistry, The Islamia University of Bahawalpur, Bahawalpur 63100 (Pakistan); Azhar Khan, Muhammad [Department of Physics, The Islamia University of Bahawalpur, Bahawalpur 63100 (Pakistan); Nasar, Gulfam; Mahmood, Azhar; Shahid, Muhammad [Department of Chemistry, The Islamia University of Bahawalpur, Bahawalpur 63100 (Pakistan); Shakir, Imran [Deanship of Scientific Research, College of Engineering, PO Box 800, King Saud University, Riyadh 11421 (Saudi Arabia); Farooq Warsi, Muhammad, E-mail: farooq.warsi@iub.edu.pk [Department of Chemistry, The Islamia University of Bahawalpur, Bahawalpur 63100 (Pakistan)

    2015-11-01

    Dy{sup 3+} and Fe{sup 3+} co-doped LaCoO{sub 3} perovskite nanoparticles were prepared by chemical co-precipitation route. Structural elucidation was carried out by thermo gravimetric analysis (TGA), X-ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier transform infrared (FTIR) spectroscopy. The data of all these characterization techniques confirmed the orthorhombic phase with particles size in the range of 20–60 nm. The magnetic parameters, DC-resistivity and dielectric properties were measured for La{sub 1−x}Dy{sub x}Co{sub 1−y}Fe{sub y}O{sub 3} nanoparticles. The purpose of all these application studies was to evaluate the prepared materials for practical applications. The substitution of Dy{sup 3+} and Fe{sup 3+} with La{sup 3+} and Co{sup 3+} respectively greatly influenced the magnetic, DC-resistivity and dielectric parameters. - Highlights: • La{sub 1−x}Dy{sub x}Co{sub 1−y}Fe{sub y}O{sub 3} nanoparticles were prepared in the range 20–60 nm. • 12 Fold increase in DC resistivity achieved for La{sub 0.40}Dy{sub 0.60}Co{sub 0.40}Fe{sub 0.60}O{sub 3.} • Paramagnetic to ferromagnetic behavior was observed for La{sub 1−x}Dy{sub x}Co{sub 1−y}Fe{sub y}O{sub 3} nanoparticles.

  17. Fundamentals of preparative and nonlinear chromatography

    Energy Technology Data Exchange (ETDEWEB)

    Guiochon, Georges A [ORNL; Felinger, Attila [ORNL; Katti, Anita [University of Tennessee, Knoxville (UTK) & Oak Ridge National Laboratory (ORNL); Shirazi, Dean G [unknown

    2006-02-01

    The second edition of Fundamentals of Preparative and Nonlinear Chromatography is devoted to the fundamentals of a new process of purification or extraction of chemicals or proteins widely used in the pharmaceutical industry and in preparative chromatography. This process permits the preparation of extremely pure compounds satisfying the requests of the US Food and Drug Administration. The book describes the fundamentals of thermodynamics, mass transfer kinetics, and flow through porous media that are relevant to chromatography. It presents the models used in chromatography and their solutions, discusses the applications made, describes the different processes used, their numerous applications, and the methods of optimization of the experimental conditions of this process.

  18. Study of the influence of substrate temperature on structural, optical, and electrical properties of Zn-doped MnIn2S4 thin films prepared by chemical spray pyrolysis

    Science.gov (United States)

    Kennedy, A.; Viswanathan, K.; Pradeev raj, K.

    2016-08-01

    The Zn-doped MnIn2S4 thin films were deposited by chemical spray pyrolysis technique on a heated glass substrate using the aqueous solution of MnCl2, InCl3, (NH2)2CS and ZnCl2. The thin films were grown at different substrate temperatures ranging from 250-400 °C. The synthesized films were characterized by X-ray diffraction (XRD), energy dispersive analysis spectrum (EDS), field emission scanning electron microscope (FESEM), UV-Vis absorption spectroscopy and four probe method. The XRD analysis indicates Zn-doped MnIn2S4 thin films were polycrystalline in nature with a cubic spinel structure having (101) plane as the preferred orientation. The structural parameters like crystalline size (D), dislocation density (δ), strain (ε) and lattice distortion (LD) have been evaluated from XRD results. The energy dispersive analysis spectrum (EDS) predicts the presence of Mn, In, S and Zn in the film grown at 250 °C. The formation of the needle and spherical shaped grains was clearly observed from FE-SEM analysis. From the optical studies, it is analyzed that about (88%) of light transmission occurs in the Vis-IR regions. It is interesting to note that the structural homogeneity and crystallinity of the films has improved due to the decrease in the absorption coefficient (α) and extinction coefficient (K) with an increase in substrate temperature. The calculated optical band gap energies increase (1.51-1.74 eV) with an increase of substrate temperatures. The photoluminescence (PL) spectrum reveals the presence of well-defined band edge (<400 nm) and defect emissions in the wavelength region around 400-650 nm. Moreover, from electrical studies, the electrical resistivity decreases with increase in substrate temperature and a minimum electrical resistivity of 1.20 ×103 Ωm was obtained for the film coated at 400 °C. The high absorption coefficient (α) in the order of 104cm-1 and high transmittance (88%) of the films makes them an efficient absorber and a good window

  19. Nanocrystalline CdS{sub 1−x}Se{sub x} alloys as thin films prepared by chemical bath deposition: Effect of x on the structural and optical properties

    Energy Technology Data Exchange (ETDEWEB)

    Sanchez-Ramirez, E.A. [Escuela Superior de Ingeniería Química e Industrias Extractivas, Instituto Politécnico Nacional, CP 07738, México D.F. (Mexico); Hernandez-Perez, M.A., E-mail: mhernandezp0606@ipn.mx [Escuela Superior de Ingeniería Química e Industrias Extractivas, Instituto Politécnico Nacional, CP 07738, México D.F. (Mexico); Aguilar-Hernandez, J. [Escuela Superior de Física y Matemáticas, Instituto Politécnico Nacional, CP 07738, México D.F. (Mexico); Rangel-Salinas, E. [Escuela Superior de Ingeniería Química e Industrias Extractivas, Instituto Politécnico Nacional, CP 07738, México D.F. (Mexico)

    2014-12-05

    Highlights: • CdS1−xSe{sub x} films with tunable structural and optical properties were grown by CBD. • Thin films are composed by a solid solution of the CdS{sub 1−x}Se{sub x} ternary alloy. • Crystal size, band gap and photoluminescence signal, decrease with the composition. • Ternary alloys show hexagonal phase with preferential orientation on (0 0 2) plane. • Films with x ⩾ 0.5 show semi-spherical grains composed by nanoworms structures. - Abstract: CdS{sub 1−x}Se{sub x} thin films were deposited on Corning glass substrates at 75 °C by chemical bath deposition (CBD) varying the composition “x” from 0 to 1 at a constant deposition time of 120 min. The composition of the films was adjusted by modifying the concentration as well as the ratio of the precursors. The morphological, compositional, structural and optical properties of the films were analyzed using several techniques such as Scanning Electron Microscopy (SEM), Energy Dispersive Spectroscopy (EDS), X-ray Diffraction (XRD), UV–Vis Spectroscopy (UV–Vis) and Photoluminescence (PL). The films grow as layers following the ion by ion mechanism, the density of the films decreases with x. Films are constituted by clusters (100–600 nm in diameter) of semispherical particles with sizes fluctuating from 10 to 20 nm. For x ⩾ 0.5 the particles are well-arranged in a “worm-like” structure. All the films are polycrystalline, to x = 0 (CdS) the cubic phase is present, the increase of composition promotes the formation of hexagonal phase or a mixture of both cubic and hexagonal phases. Preferential orientation in the (1 0 0) or (0 0 2) plane is observed. The crystal size decreases from 20 to 6 nm when x is increased. The optical properties can be easily tuned by adjusting the composition. Optical absorption analysis shows that the band gap (E{sub g}) value shifts to red in function of x (from 2.47 to 1.99 eV). Photoluminescence signal changes as “x” varies showing a regular behavior

  20. Study on Preparation and Properties of High Purity MgSe Polycrystalline by Chemical Vapor Synthesizing%高纯MgSe多晶的化学气相合成及特性研究

    Institute of Scientific and Technical Information of China (English)

    李辉斌; 李焕勇; 付泽华; 田世俊

    2013-01-01

    MgSe polycrystalline were grown by chemical vapor transport ( CVT) method, using Mg and Se elements as the raw materials and NH4C1 as the transport agent, respectively. The temperature range for synthesizing samples are from 999 ℃ to 992 ℃. The as-grown MgSe polycrystalline were characterized by XRD, UV-VIS-NIR spectrophotometer, infrared spectrometer and photoluminescence for their structures and optical properties. The results indicate the product is MgSe polycrystalline, which have NaCl structure, the Eg of MgSe polycrystalline is 1.98 eV. Two emission bands were detected around 1.6 eV, which can be attributed to donoracceptor recombination. The results prove that growing MgSe polycrystalline in one step from magnesium and selenium with the assistance of NH4G1 reaction accelerator is a good method.%以高纯Mg、Se单质为原料,NH4Cl作反应促进剂,温度为999~992℃,采用化学气相输运法(CVT)成功合成出MgSe多晶.采用X射线粉末衍射仪、紫外-可见-近红外分光光度计、傅立叶变换红外光谱仪以及光致发光测试系统研究了MgSe多晶的结构和光学特性.结果表明:合成物为MgSe多晶,具有NaCl型结构,禁带宽度Eg为1.98eV,在1.6eV附近内存在与施主-受主对辐射复合发光相关的发光带.研究证明由Mg、Se单质在促进剂NH4Cl辅助下直接合成MgSe多晶是一种较好的方法.