WorldWideScience

Sample records for iodates

  1. CONCENTRATION OF Pu USING AN IODATE PRECIPITATE

    Science.gov (United States)

    Fries, B.A.

    1960-02-23

    A method is given for separating plutonium from lanthanum in a lanthanum fluoride carrier precipitation process for the recovery of plutonium values from an aqueous solution. The carrier precipitation process includes the steps of forming a lanthanum fluoride precipi- . tate, thereby carrying plutonium out of solution, metathesizing the fluoride precipitate to a hydroxide precipitate, and then dissolving the hydroxide precipitate in nitric acid. In accordance with the invention, the nitric acid solution, which contains plutonium and lanthanum, is made 0.05 to 0.15 molar in potassium iodate. thereby precipitating plutonium as plutonous iodate and the plutonous iodate is separated from the lanthanum- containing supernatant solution.

  2. A Facile Spectrophotometric Method for the Determination of Iodate ...

    African Journals Online (AJOL)

    A simple spectrophotometric method has been developed for the determination of iodate in table salt samples using thionin or azure B. The method is based on the reaction of iodate with potassium iodide in an acid medium to liberate iodine. The liberated iodine bleaches the violet colour of thionin or azure B, which are ...

  3. urinary iodine concentration and availability of iodated salt in school

    African Journals Online (AJOL)

    2006-04-01

    Apr 1, 2006 ... Request for reprints to: K.B.M. Kulwa, Department of Food Science and Technology, Sokoine University of Agriculture,. PO. ... content of salt especially in the rural areas where informal re-packing of iodated salt and sale, of non-iodated salt are ... research, capacity building, advocacy and public information ...

  4. Removal of active iodine/iodate from liquid wastes

    International Nuclear Information System (INIS)

    Jones, C.P.; Turner, A.D.; Kavanagh, P.R.

    1991-03-01

    The work described in this report has involved the development of two techniques, ultrafiltration (UF) and electrochemical ion exchange (EIX), for the removal of active iodine/iodate from aqueous wastes. (author)

  5. Elaboration and characterization of an iodate-substituted hydroxyapatite cement

    International Nuclear Information System (INIS)

    Coulon, A.; Campayo, L.; Laurencin, D.; Grandjean, A.; Cau Dit Coumes, C.; Rossignol, S.

    2015-01-01

    In the last decades, robust host matrices have been developed to guarantee a durable confinement of some of the most mobile radionuclides. In this work, we describe a novel method for iodine incorporation into an iodate-substituted hydroxyapatite by means of a cementation route. Such a material is obtained from a stoichiometric mixture of tetra-calcium-phosphate (TTCP)/tricalcium-phosphate (αTCP)/sodium iodate with a molar ratio 1/2/0.5. This material corresponds to an iodine incorporation content ∼6.5 wt.%. The evolution of this system during the early age (followed by calorimetric and conductimetric measurements) was compared to the same cementitious system without iodate. Results show that sodium iodate acts as a retarder that can be appropriate to control setting for an industrial application. The delay is due to the precipitation of non-cohesive intermediate phases like calcium iodate that are then totally consumed when the crystallization of hydroxyapatite occurs. At later age, a porous bulk material consisting of traces of TTCP and αTCP particles covered by needles is obtained. The composition of these needles is in agreement with that of the desired iodate-containing apatite. (authors)

  6. Distribution of iodate in the south western Bay of Bengal

    Digital Repository Service at National Institute of Oceanography (India)

    Raju, G.R.K.; Rajendran, A.; Reddy, C.V.G.

    role in surface waters in the iodine system. A mole ratio of NO :PO :IO was found to be 94:10:1. Depletion of iodate, calculated in 2 ways, showed a linear model with the depletion of other nutrients in surface waters (above oxycline) suggesting a...

  7. Effects of Potassium Iodate Application on the Biomass and Iodine ...

    African Journals Online (AJOL)

    Jane

    The increase in iodine concentration in water leaf ranged from 61.59 ± 0.24 to 73.41 ± 0.83. µg/100 g in week 4 and 62.06 ± 0.09 to 96.25 ± 0.025 µg/100 g in week 6. From the results, the vegetables treated with 40 µg/l potassium iodate showed the highest iodine level in week 4. These results from this iodine biofortification ...

  8. Growth and study of some gel grown group II single crystals of iodate

    Indian Academy of Sciences (India)

    Unknown

    The effect of doping was studied using IR spectroscopy and thermal analysis. Keywords. Silica gel; barium iodate; calcium iodate; XRD; FT-IR; TGA/DTA. 1. .... Table 2. Effect of concentration of reactants on habit quality and size of BaIO3 crystals. Conc. of reactant in gel. Conc. of reactant above gel. Habit. Quality. Size. (mm).

  9. Growth and study of some gel grown group II single crystals of iodate

    Indian Academy of Sciences (India)

    Unknown

    Page 1 ... Abstract. Single crystals of calcium iodate and barium iodate were grown by simple gel technique by single diffusion method. The optimum conditions were established by varying various parameters such as pH of gel solution, gel concentration, gel setting time, concentration of the reactants etc. Crystals having ...

  10. Iodate in inshore and offshore waters of Central Bay of Bengal

    Digital Repository Service at National Institute of Oceanography (India)

    Sarma, V.V.

    Biological stripping of iodate in the surface waters is noticed in the inshore and offshore waters of Bay of Bengal. A good correlation is observed between iodate and phosphate and nitrate and the molar ratios determined being NO3: PO4: IO3 = 88...

  11. Scrubbing of iodine from gas streams with mercuric nitrate-conversion of mercuric iodate product to barium iodate for fixation in concrete

    Energy Technology Data Exchange (ETDEWEB)

    Rogers, G.C.; Moore, J.G.; Morgan, M.T.

    1980-06-01

    A bench-scale model of a mercuric nitrate scrubber for removal of iodine from off-gas streams was constructed and operated in conjunction with a mercuric iodate-to-barium iodate conversion system to determine the feasibility of total recycle of all processing solutions. The two main aspects of the system examined were (1) the extent of contamination of the barium iodate product, and (2) the effect of cross-contamination of various process solutions on the efficiency of the process. The experimental evidence obtained indicates that, with appropriate control, all solutions can be recycled without significant contamination of the product that would be harmful to the host concrete or to the environment. Mercury contamination was found to be less than or equal to 0.5 wt % of the barium iodate product. The most significant effect on system efficiency was determined to be barium hydroxide contamination of the sodium hydroxide solution used to convert mercuric iodate to sodium iodate. A mole ratio of barium hydroxide to sodium hydroxide of about 1:225 caused a decrease in conversion efficiency of about 45%.

  12. Removal and distribution of iodate in mangrove environment

    International Nuclear Information System (INIS)

    Machado, E.C; Machado, W; Sanders, L.F; Bellido, L.F; Patchineelam, S.R; Bellido Jr, A.V

    2003-01-01

    Retention experiments were carried out in laboratory in order to investigate the iodate ion removal from tidal water by the underlying creek sediment, as well as, distribution in the mangrove sediment of Sepetiba Bay, Rio de Janeiro. Local tidal water spiked with 131 IO 3 was added to several cores containing 6-7 cm of mangrove sediment. A sample solution was taken everyday for 8□9 days and assayed by means of a high purity germanium detector coupled to a multichannel analyser. It was found that, after two days, around 56 % of the radioiodate was taken up by the sediment. At the end of the experiment, the sediment was sectioned in 1-cm layers and also analyzed by gamma spectrometry. The overall results, in seven cores, showed that 89% of initial 131 IO 3 activities were transferred to sediment, whereas 78% of the total activity was within the first cm of the upper layer. It seems from the determination of total organic matter content, that the organic matter present in the Sepetiba's mangrove sediment, have a substantial influence in the iodate removal from the water column (author)

  13. Removal of active iodine/iodate from liquid wastes

    International Nuclear Information System (INIS)

    Jones, C.P.; Kavanagh, P.R.; Turner, A.D.

    1992-01-01

    The presence of abnormally high levels of the radioactive isotope of iodine, 125 I, has been discovered in the thyroid glands taken from swans found on the Rivers Thames and Trent. The sources of activity have been traced to sewage outfalls into the rivers. It has been postulated that the 125 I enters the system from local hospitals and research establishments where radio-labelled proteins are produced. The chemical nature of the iodine depends upon the conditions to which it is exposed. The work described in this report has involved the development of two techniques, ultrafiltration and electrochemical ion exchange, for the removal of active iodine/iodate from aqueous wastes. The report also contains details relating to an electrochemical flow cell designed to convert iodate to iodide prior to ultrafiltration treatment. A comparison is then made between the two techniques. The initial target of decontamination factor of 10 has been exceeded by both methods. The consideration of solution pH and ion selectivity has resulted in the design and demonstration of a single CAEIX cell capable of attaining decontamination factors in excess of 33. The filtration technique requires a two stage precipitation using calcium ions to remove free phosphate and then silver ions to precipitate iodide. The rather high solids production of at least 10g/dm 3 of treated waste is, to an extent, offset by the high DF value obtained, 174. (Author)

  14. Photolysis of frozen iodate salts as a source of active iodine in the polar environment

    Directory of Open Access Journals (Sweden)

    Ó. Gálvez

    2016-10-01

    Full Text Available Reactive halogens play a key role in the oxidation capacity of the polar troposphere. However, sources and mechanisms, particularly those involving active iodine, are still poorly understood. In this paper, the photolysis of an atmospherically relevant frozen iodate salt has been experimentally studied using infrared (IR spectroscopy. The samples were generated at low temperatures in the presence of different amounts of water. The IR spectra have confirmed that, under near-ultraviolet–visible (UV–Vis radiation, iodate is efficiently photolysed. The integrated IR absorption coefficient of the iodate anion on the band at 750 cm−1 has been measured to be A  =  9.8 ± 0.5  ×  10−17 cm molecule−1. The photolysis rate of the ammonium iodate salt was measured by monitoring the decay of ammonium or iodate IR bands (1430 and 750 cm−1 respectively in the presence of a solar simulator. The absorption cross section of the liquid solutions of ammonium iodate at wavelengths relevant for the troposphere (250 to 400 nm has been obtained and used to estimate the photolytic quantum yield for the frozen salt. Finally, using an atmospheric model, constrained with the experimental data, we suggest that the photolysis of iodate in frozen salt can potentially provide a pathway for the release of active iodine to the polar atmosphere.

  15. Modelling iodide – iodate speciation in atmospheric aerosol: Contributions of inorganic and organic iodine chemistry

    Directory of Open Access Journals (Sweden)

    S. Pechtl

    2007-01-01

    Full Text Available The speciation of iodine in atmospheric aerosol is currently poorly understood. Models predict negligible iodide concentrations but accumulation of iodate in aerosol, both of which is not confirmed by recent measurements. We present an updated aqueous phase iodine chemistry scheme for use in atmospheric chemistry models and discuss sensitivity studies with the marine boundary layer model MISTRA. These studies show that iodate can be reduced in acidic aerosol by inorganic reactions, i.e., iodate does not necessarily accumulate in particles. Furthermore, the transformation of particulate iodide to volatile iodine species likely has been overestimated in previous model studies due to negligence of collision-induced upper limits for the reaction rates. However, inorganic reaction cycles still do not seem to be sufficient to reproduce the observed range of iodide – iodate speciation in atmospheric aerosol. Therefore, we also investigate the effects of the recently suggested reaction of HOI with dissolved organic matter to produce iodide. If this reaction is fast enough to compete with the inorganic mechanism, it would not only directly lead to enhanced iodide concentrations but, indirectly via speed-up of the inorganic iodate reduction cycles, also to a decrease in iodate concentrations. Hence, according to our model studies, organic iodine chemistry, combined with inorganic reaction cycles, is able to reproduce observations. The presented chemistry cycles are highly dependent on pH and thus offer an explanation for the large observed variability of the iodide – iodate speciation in atmospheric aerosol.

  16. Investigation of iodine liberation process in redox titration of potassium iodate with sodium thiosulfate

    International Nuclear Information System (INIS)

    Asakai, Toshiaki; Hioki, Akiharu

    2011-01-01

    Potassium iodate is often used as a reference material to standardize a sodium thiosulfate solution which is a familiar titrant for redox titrations. In the standardization, iodine (triiodide) liberated by potassium iodate in an acidic potassium iodide solution is titrated with a sodium thiosulfate solution. The iodine liberation process is significantly affected by the amount of acid, that of potassium iodide added, the waiting time for the liberation, and light; therefore, the process plays a key role for the accuracy of the titration results. Constant-voltage biamperometry with a modified dual platinum-chip electrode was utilized to monitor the amount of liberated iodine under several liberation conditions. Coulometric titration was utilized to determine the concentration of a sodium thiosulfate solution on an absolute basis. Potassium iodate was assayed by gravimetric titration with the sodium thiosulfate solution under several iodine liberation conditions. The liberation process was discussed from the changes in the apparent assay of potassium iodate. The information of the appropriate titration procedure obtained in the present study is useful for any analysts utilizing potassium iodate to standardize a thiosulfate solution.

  17. Improved salt iodation methods for small-scale salt producers in low-resource settings in Tanzania

    Directory of Open Access Journals (Sweden)

    Assey Vincent D

    2009-06-01

    Full Text Available Abstract Background Universal salt iodation will prevent iodine deficiency disorders (IDD. Globally, salt-iodation technologies mostly target large and medium-scale salt-producers. Since most producers in low-income countries are small-scale, we examined and improved the performance of hand and knapsack-sprayers used locally in Tanzania. Methods We studied three salt facilities on the Bagamoyo coast, investigating procedures for preparing potassium-iodate solution, salt spraying and mixing. Different concentrations of solution were prepared and tested using different iodation methods, with the aim of attaining correct and homogeneous iodine levels under real-life conditions. Levels achieved by manual mixing were compared to those achieved by machine mixing. Results The overall median iodation level in samples of salt iodated using previously existing methods was 10.6 ppm (range 1.1 – 110.0 ppm, with much higher levels in the top than the bottom layers of the salt bags, p Conclusion Supervised, standardized salt iodation procedures adapted to local circumstances can yield homogeneous iodine levels within the required range, overcoming a major obstacle to universal salt iodation.

  18. Iodate and nitrate transformation by Agrobacterium/Rhizobium related strain DVZ35 isolated from contaminated Hanford groundwater.

    Science.gov (United States)

    Lee, Brady D; Ellis, Joshua T; Dodwell, Alex; Eisenhauer, Emalee E R; Saunders, Danielle L; Lee, M Hope

    2018-02-06

    Nitrate and radioiodine ( 129 I) contamination is widespread in groundwater underneath the Central Plateau of the Hanford Site. 129 I, a byproduct of nuclear fission, is of concern due to a 15.7 million year half-life, and toxicity. The Hanford 200 West Area contains plumes covering 4.3 km 2 with average 129 I concentrations of 3.5 pCi/L. Iodate accounts for 70.6% of the iodine present and organo-iodine and iodide make up 25.8% and 3.6%, respectively. Nitrate plumes encompassing the 129 I plumes have a surface area of 16 km 2 averaging 130 mg/L. A nitrate and iodate reducing bacterium closely related to Agrobacterium, strain DVZ35, was isolated from sediment incubated in a 129 I plume. Iodate removal efficiency was 36.3% in transition cultures, and 47.8% in anaerobic cultures. Nitrate (10 mM) was also reduced in the microcosm. When nitrate was spiked into the microcosms, iodate removal efficiency was 84.0% and 69.2% in transition and anaerobic cultures, respectively. Iodate reduction was lacking when nitrate was absent from the growth medium. These data indicate there is simultaneous reduction of nitrate and iodate by DVZ35, and iodate is reduced to iodide. Results provide the scientific basis for combined nitrogen and iodine cycling throughout the Hanford Site. Copyright © 2018. Published by Elsevier B.V.

  19. Study of iodine-iodate isotopic exchange reaction in neutral aqueous solutions by radiotracer technique

    International Nuclear Information System (INIS)

    Tripathi, R.; Ram, K.D.

    1993-01-01

    The isotopic exchange of iodine atoms in neutral aqueous solutions of iodate ions and iodine (in KI) is found to obey the rate law R = k [IO 3 - ] 0.4 [I 2 ] 1.2 at 175 o C. The addition of neutral ionic salts, e.g. KCl and KNO 3 , in the reaction mixture showed a slight catalytic effect on the exchange rate. Further, the kinetic salt effect indicated the involvement of at least one neutral species on the rate-determining step. The activation energy in neutral aqueous solutions of iodate ions and iodine is found to be 86 ± 3 kJ mol -1 , which decreases in the presence of KCl (79 ± 3 kJ mol -1 and KNO 3 (82 + 3 kJ mol -1 ). The activation parameters, viz. free energy of activation, enthalpy of activation and entropy of activation, were also calculated. Based on these results, an association-dissociation type of reaction mechanism is proposed for this exchange reaction in neutral aqueous medium, similar to that proposed earlier for iodide-iodate isotopic exchange reaction in neutral aqueous solutions, nitrate eutectic melts and iodide-iodate melts. (author)

  20. Growth and study of mixed crystals of Ca–Cd iodate

    Indian Academy of Sciences (India)

    Wintec

    Abstract. Mixed crystals of calcium–cadmium iodate were grown by a simple gel technique using diffusion method. The optimum conditions were established by varying various parameters such as pH of gel solution, gel concentration, gel setting time, concentration of reactants etc. Crystals having different morphologies and.

  1. Iodate and iodo-trihalomethane formation during chlorination of iodide-containing waters: role of bromide.

    Science.gov (United States)

    Criquet, Justine; Allard, Sebastien; Salhi, Elisabeth; Joll, Cynthia A; Heitz, Anna; von Gunten, Urs

    2012-07-03

    The kinetics of iodate formation is a critical factor in mitigation of the formation of potentially toxic and off flavor causing iodoorganic compounds during chlorination. This study demonstrates that the formation of bromine through the oxidation of bromide by chlorine significantly enhances the oxidation of iodide to iodate in a bromide-catalyzed process. The pH-dependent kinetics revealed species specific rate constants of k(HOBr + IO(-)) = 1.9 × 10(6) M(-1) s(-1), k(BrO(-) + IO(-)) = 1.8 × 10(3) M(-1) s(-1), and k(HOBr + HOI) < 1 M(-1) s(-1). The kinetics and the yield of iodate formation in natural waters depend mainly on the naturally occurring bromide and the type and concentration of dissolved organic matter (DOM). The process of free chlorine exposure followed by ammonia addition revealed that the formation of iodo-trihalomethanes (I-THMs), especially iodoform, was greatly reduced by an increase of free chlorine exposure and an increase of the Br(-)/I(-) ratio. In water from the Great Southern River (with a bromide concentration of 200 μg/L), the relative I-incorporation in I-THMs decreased from 18 to 2% when the free chlorine contact time was increased from 2 to 20 min (chlorine dose of 1 mg Cl(2)/L). This observation is inversely correlated with the conversion of iodide to iodate, which increased from 10 to nearly 90%. Increasing bromide concentration also increased the conversion of iodide to iodate: from 45 to nearly 90% with a bromide concentration of 40 and 200 μg/L, respectively, and a prechlorination time of 20 min, while the I-incorporation in I-THMs decreased from 10 to 2%.

  2. Polarographic determination of Iodide and Iodate, in Solutions Coming from Aerosols in Fission Products Containment Studies in Nuclear Power Stations

    International Nuclear Information System (INIS)

    Sanchez, M.; Ballesteros, O.; Fernandez, M.; Clavero, M.A.; Gonzalez, A.M.

    2000-01-01

    A polarographic method is described for the iodine species determination, iodide and iodate in water solutions. the iodate can be determined by differential pulse polarography. Calibration curves and the detection and determination limits have been obtained. Iodides is oxidized to iodate with sodium hypochlorite and the excess of oxidizing agent is destroyed with sodium sulphide. The concentration of iodide is calculated as the difference between the concentration of iodate in the sample before and after the oxidation. As an application, species of iodine in samples coming from the experimental plants GIRS (Gaseous Iodine Removal by Sprays) of Nuclear Fission Department of the CIEMAT, dedicated to fission products containment studies in nuclear power station, were determined. (Author) 10 refs

  3. Recoil chemistry in inorganic solids with simultaneous activation of anion and cation: indium iodate system [ Paper No. NC-14

    International Nuclear Information System (INIS)

    Recoil chemistry of indium iodate has been worked out along with that of indium sulphate and potassium iodate with a view to find out the role of hot atoms of cation and anion being activated simultaneously. The chemical identification and separation has been presented in this paper along with some preliminary results on retention and yield of different hot species produced under (n,γ) process. (author)

  4. Metal Iodate-Based Energetic Composites and Their Combustion and Biocidal Performance.

    Science.gov (United States)

    Wang, H; Jian, G; Zhou, W; DeLisio, J B; Lee, V T; Zachariah, M R

    2015-08-12

    The biological agents that can be weaponized, such as Bacillus anthracis, pose a considerable potential public threat. Bacterial spores, in particular, are highly stress resistant and cannot be completely neutralized by common bactericides. This paper reports on synthesis of metal iodate-based aluminized electrospray-assembled nanocomposites which neutralize spores through a combined thermal and chemical mechanism. Here metal iodates (Bi(IO3)3, Cu(IO3)2, and Fe(IO3)3) act as a strong oxidizer to nanoaluminum to yield a very exothermic and violent reaction, and simultaneously generate iodine as a long-lived bactericide. These microparticle-assembled nanocomposites when characterized in terms of reaction times and temporal pressure release show significantly improved reactivity. Furthermore, sporicidal performance superior to conventional metal-oxide-based thermites clearly shows the advantages of combining both a thermal and biocidal mechanism in spore neutralization.

  5. Growth and study of mixed crystals of Ca–Cd iodate

    Indian Academy of Sciences (India)

    Wintec

    due to loss of coordinated 2 water molecules. There is no further weight loss up to 580°C. Further 65% weight loss in the temperature range 580–670°C is due to decomposi- tion of crystals and may be loss of iodine and some oxy- gen from the anhydrous mixed iodate crystals. Again in the temperature range 700–760°C, ...

  6. Tanzania national survey on iodine deficiency: impact after twelve years of salt iodation

    Directory of Open Access Journals (Sweden)

    Kimboka Sabas

    2009-09-01

    Full Text Available Abstract Background In many low-income countries, children are at high risk of iodine deficiency disorders, including brain damage. In the early 1990s, Tanzania, a country that previously suffered from moderate to severe iodine deficiency, adopted universal salt iodation (USI as an intervention strategy, but its impact remained unknown. Methods We report on the first national survey in mainland Tanzania, conducted in 2004 to assess the extent to which iodated salt was used and its apparent impact on the total goitre prevalence (TGP and urinary iodine concentrations (UIC among the schoolchildren after USI was initiated. In 2004, a cross-sectional goitre survey was conducted; covering 140,758 schoolchildren aged 6 - 18 years were graded for goitre according to new WHO goitre classification system. Comparisons were made with district surveys conducted throughout most of the country during the 1980s and 90s. 131,941 salt samples from households were tested for iodine using rapid field test kits. UIC was determined spectrophotometrically using the ammonium persulfate digestion method in 4523 sub-sampled children. Results 83.6% (95% CI: 83.4 - 83.8 of salt samples tested positive for iodine. Whereas the TGP was about 25% on average in the earlier surveys, it was 6.9% (95%CI: 6.8-7.0 in 2004. The TGP for the younger children, 6-9 years old, was 4.2% (95%CI: 4.0-4.4, n = 41,965. In the 27 goitre-endemic districts, TGP decreased from 61% (1980s to 12.3% (2004. The median UIC was 204 (95% CF: 192-215 μg/L. Only 25% of children had UIC Conclusion Our study demonstrates a marked improvement in iodine nutrition in Tanzania, twelve years after the initiation of salt iodation programme. The challenge in sustaining IDD elimination in Tanzania is now two-fold: to better reach the areas with low coverage of iodated salt, and to reduce iodine intake in areas where it is excessive. Particular attention is needed in improving quality control at production level and

  7. Determination of iodide, iodate and organo-iodine in waters with a new total organic iodine measurement approach.

    Science.gov (United States)

    Gong, Tingting; Zhang, Xiangru

    2013-11-01

    The dissolved iodine species that dominate aquatic systems are iodide, iodate and organo-iodine. These species may undergo transformation to one another and thus affect the formation of iodinated disinfection byproducts during disinfection of drinking waters or wastewater effluents. In this study, a fast, sensitive and accurate method for determining these iodine species in waters was developed by derivatizing iodide and iodate to organic iodine and measuring organic iodine with a total organic iodine (TOI) measurement approach. Within this method, organo-iodine was determined directly by TOI measurement; iodide was oxidized by monochloramine to hypoiodous acid and then hypoiodous acid reacted with phenol to form organic iodine, which was determined by TOI measurement; iodate was reduced by ascorbic acid to iodide and then determined as iodide. The quantitation limit of organo-iodine or sum of organo-iodine and iodide or sum of organo-iodine, iodide and iodate was 5 μg/L as I for a 40 mL water sample (or 2.5 μg/L as I for an 80 mL water sample, or 1.25 μg/L as I for a 160 mL water sample). This method was successfully applied to the determination of iodide, iodate and organo-iodine in a variety of water samples, including tap water, seawater, urine and wastewater. The recoveries of iodide, iodate and organo-iodine were 91-109%, 90-108% and 91-108%, respectively. The concentrations and distributions of iodine species in different water samples were obtained and compared. Copyright © 2013 Elsevier Ltd. All rights reserved.

  8. Chemical dosimetry using an iodide/iodate aqueous solution: application to the gamma irradiation of blood

    Energy Technology Data Exchange (ETDEWEB)

    Rahn, Ronald O. E-mail: rahnr@ms.soph.uab.edu

    2003-01-01

    A method is presented for measuring and verifying the radiation dose in gamma irradiators used for treating blood prior to transfusion. This method employs the iodide/iodate dosimeter (0.6 M iodide, 0.1 M iodate, and 0.01 borate at pH 9.25) which forms triiodide upon exposure to ionizing radiation; for Cs-137 radiation the G value is 14.1. Samples were placed in a canister and irradiated in a conventional blood bank irradiator containing several Cs-137 sources. The following were exposed: (a) nine 1.5 ml plastic tubes containing dosimetry solution taped inside a 250 ml blood bag, which, in turn, was filled with either water or blood, (b) 50 ml plastic syringes containing varying amounts of dosimetry solution, (c) a whole blood bag containing 250 ml of the dosimetry solution. A water phantom was not used during exposure. The absorbance changes at 352 nm due to triiodide formation were used to determine a dose rate, which was on the order of 10 Gy/min ({+-}5%) for all samples measured. This value is consistent with an average time-decayed dose rate for the irradiation volume as determined from the manufacturers calibration of the unit taking into account the heterogeneous nature of the radiation field inside the irradiator and the absence of a water phantom. Because of its sensitivity, ease of operation, and reproducibility, it is suggested that the iodide/iodate dosimetry system be considered for on-site periodic conformation/verification of the radiation dose as part of a quality assurance requirement for blood irradiators.

  9. Chemical dosimetry using an iodide/iodate aqueous solution: application to the gamma irradiation of blood

    International Nuclear Information System (INIS)

    Rahn, Ronald O.

    2003-01-01

    A method is presented for measuring and verifying the radiation dose in gamma irradiators used for treating blood prior to transfusion. This method employs the iodide/iodate dosimeter (0.6 M iodide, 0.1 M iodate, and 0.01 borate at pH 9.25) which forms triiodide upon exposure to ionizing radiation; for Cs-137 radiation the G value is 14.1. Samples were placed in a canister and irradiated in a conventional blood bank irradiator containing several Cs-137 sources. The following were exposed: (a) nine 1.5 ml plastic tubes containing dosimetry solution taped inside a 250 ml blood bag, which, in turn, was filled with either water or blood, (b) 50 ml plastic syringes containing varying amounts of dosimetry solution, (c) a whole blood bag containing 250 ml of the dosimetry solution. A water phantom was not used during exposure. The absorbance changes at 352 nm due to triiodide formation were used to determine a dose rate, which was on the order of 10 Gy/min (±5%) for all samples measured. This value is consistent with an average time-decayed dose rate for the irradiation volume as determined from the manufacturers calibration of the unit taking into account the heterogeneous nature of the radiation field inside the irradiator and the absence of a water phantom. Because of its sensitivity, ease of operation, and reproducibility, it is suggested that the iodide/iodate dosimetry system be considered for on-site periodic conformation/verification of the radiation dose as part of a quality assurance requirement for blood irradiators

  10. Iodide and iodate effects on the growth and fruit quality of strawberry.

    Science.gov (United States)

    Li, Rui; Liu, Hui-Ping; Hong, Chun-Lai; Dai, Zi-Xi; Liu, Jia-Wei; Zhou, Jun; Hu, Chun-Qing; Weng, Huan-Xin

    2017-01-01

    Iodine deficiency is an environmental health problem affecting one-third of the global population. An iodine biofortification hydroponic experiment was conducted to explore the iodide and iodate uptake characteristics of strawberry plants, to measure the dosage effects of iodine on plant growth and to evaluate the influence of I - or IO 3 - application on fruit quality. After biofortification, the iodine contents of the fresh strawberry fruits were 600-4000 µg kg -1 , covering the WHO dietary iodine allowance of 150 µg · day -1 for adults. The iodine uptake of the strawberry plants increased with increasing I - or IO 3 - concentration of the culture solution. At the same iodine concentration, the iodate uptakes of various plant organs under I - treatments were apparently more than those under IO 3 - treatments. Low-level exogenous iodine (I - ≤ 0.25 mg L -1 or IO 3 - ≤ 0.50 mg L -1 ) not only promoted plant growth and increased biomass per plant, but also improved fruit quality by enhancing the vitamin C and soluble sugar contents of the strawberry fruits. Nevertheless, excessive exogenous iodine inhibited plant growth and reduced biomass per plant. IO 3 - uptake apparently increased the total acidity and nitrate content of the fruits, reducing the quality of the strawberry fruits. Conversely, I - uptake obviously decreased the total acidity and nitrate content of the strawberry fruits, improving the fruit quality. The strawberry can be used as a target crop for iodine biofortification. Furthermore, applying an appropriate dose of KI can improve the fruit quality of the strawberry plants. © 2016 Society of Chemical Industry. © 2016 Society of Chemical Industry.

  11. Iodine-129 and Iodine-127 speciation in groundwater at the Hanford Site, U.S.: iodate incorporation into calcite

    International Nuclear Information System (INIS)

    Zhang, Saijin; Yeager, Chris; Wellman, Dawn M.; Santschi, Peter H.

    2013-01-01

    The Hanford Site, the most contaminated nuclear site in the United States, has large radioactive waste plumes containing high 129I levels. The geochemical transport and fate of radioiodine depends largely on its chemical speciation that is greatly affected by environmental factors. This study reports, for the first time, the speciation of stable and radioactive iodine in the groundwater from the Hanford Site. Iodate was the dominant species and accounts for up to 84%, followed by organo-iodine and minimal levels of iodide. The relatively high pH and oxidizing environment may have prevented iodate reduction. Our results identified that calcite precipitation caused by degassing of CO2 during deep groundwater sampling incorporated between 7 to 40% of dissolved iodine (including 127I and 129I) that was originally in the groundwater, transforming dissolved to particulate iodate during sampling. In order to understand the mechanisms underlying iodine incorporation by calcite, laboratory experiments were carried out to replicate this iodine sequestering processes. Two methods were utilized in this study, 1) addition of sodium carbonate; 2) addition of calcium chloride followed by sodium carbonate where the pH was well controlled at ~8.2, which is close to the average pH of Hanford Site groundwater. It was demonstrated that iodate was the main species incorporated into calcite and this incorporation process could be impeded by elevated pH and decreasing ionic strength in groundwater. This study provides critical information for predicting the long-term fate and transport of 129I at the Hanford Site and reveals a potential means for improved remediation strategies of 129I

  12. Modification of glassy carbon electrode with a polymer/mediator composite and its application for the electrochemical detection of iodate

    International Nuclear Information System (INIS)

    Li, Ta-Jen; Lin, Chia-Yu; Balamurugan, A.; Kung, Chung-Wei; Wang, Jen-Yuan; Hu, Chih-Wei; Wang, Chun-Chieh; Chen, Po-Yen; Vittal, R.; Ho, Kuo-Chuan

    2012-01-01

    Highlights: ► FAD and PEDOT are combined to modify the glassy carbon electrode for IO 3 − sensing. ► The doping of FAD into PEDOT matrix can almost be viewed as an irreversible process. ► The optimal cycle number for preparing the GCE/PEDOT/FAD electrode is found to be 9. ► The detection limit of the GCE/PEDOT/FAD electrode for IO 3 − is found to be 0.16 μM. ► The GCE/PEDOT/FAD electrode possesses enough selectivity toward IO 3 − . - Abstract: A modified glassy carbon electrode was prepared by depositing a composite of polymer and mediator on a glassy carbon electrode (GCE). The mediator, flavin adenine dinucleotide (FAD) and the polymer, poly(3,4-ethylenedioxythiophene) (PEDOT) were electrochemically deposited as a composite on the GCE by applying cyclic voltammetry (CV). This modified electrode is hereafter designated as GCE/PEDOT/FAD. FAD was found to significantly enhance the growth of PEDOT. Electrochemical quartz crystal microbalance (EQCM) analysis was performed to study the mass changes in the electrode during the electrodeposition of PEDOT, with and without the addition of FAD. The optimal cycle number for preparing the modified electrode was determined to be 9, and the corresponding surface coverage of FAD (Γ FAD ) was ca. 5.11 × 10 −10 mol cm −2 . The amperometric detection of iodate was performed in a 100 mM buffer solution (pH 1.5). The GCE/PEDOT/FAD showed a sensitivity of 0.78 μA μM −1 cm −2 , a linear range of 4–140 μM, and a limit of detection of 0.16 μM for iodate. The interference effects of 250-fold Na + , Mg 2+ , Ca 2+ , Zn 2+ , Fe 2+ , Cl − , NO 3 − , I − , SO 4 2− and SO 3 2− , with reference to the concentration of iodate were negligible. The long-term stability of GCE/PEDOT/FAD was also investigated. The GCE/PEDOT/FAD electrode retained 82% of its initial amperometric response to iodate after 7 days. The GCE/PEDOT/FAD was also applied to determine iodate in a commercial salt.

  13. Abiotic reaction of iodate with sphagnum peat and other natural organic matter

    International Nuclear Information System (INIS)

    Steinberg, S.M.; Kimble, G.; Schmett, G.T.; Emerson, D.W.; Turner, M.F.; Rudin, M.

    2008-01-01

    Previous studies have shown that iodine (including 129 I) can be strongly retained in organic-rich surface soils and sediment and that a large fraction of soluble iodine may be associated with dissolved humic material. Iodate (IO 3 - ) reacts with natural organic matter (NOM) producing either hypoiodous acid (HIO) or I 2 as an intermediate. This intermediate is subsequently incorporated into the organic matter. Based on reactions of model compounds, we infer that iodine reacts with peat by aromatic substitution of hydrogen on phenolic constituents of the peat. Alternatively, the intermediate, HIO or I 2 , may be reduced to iodide (I - ). The pH (and temperature) dependence of the IO 3 - reaction (reduction) has been explored with sphagnum peat, alkali lignin, and several model compounds. The incorporation of iodine into NOM has been verified by pyrolysis gas chromatography/mass spectrometry (GC/MS). Model compound studies indicate that reduction of IO 3 - to HIO may result from reaction with hydroquinone (or semiquinone) moieties of the peat. (author)

  14. Chemical effects of (n,2n) reactions on iodate and periodates systems

    International Nuclear Information System (INIS)

    Mendonca, J.M.A. de.

    1975-12-01

    The chemical consequences of (n,2n) reactions on cristalline sodium iodate and periodates were investigated measuring the initial yield and the post irradiation thermal annealing yields (90 0 C) of the separated fractions I - , IO 3 - and IO 4 - . NaIO 3 , NaIO 3 .H 2 O and NaIO 4 , Na 4 H 2 IO 6 , Na 4 I 2 O 9 .3H 2 O containing 127 I and 129 I, or both, were irradiated with 14 MeV neutrons. Results obtained show different effects for each system and that 126 I and 128 I isotopes keep the same behaviour in the irradiated compounds containing only α 127 I or 129 I and in compounds having both 127 I and 129 I. Neither isotope effect nor qualitative differences on thermal annealing at 90 0 C were observed. The annealed fractions in the three studied periodates were IO - 3 and IO - 4 . These results differ from the ones reported previously for (n,γ) reactions on the same compounds [pt

  15. Behavioral and anatomical abnormalities in a sodium iodate-induced model of retinal pigment epithelium degeneration.

    Science.gov (United States)

    Enzmann, Volker; Row, Barry W; Yamauchi, Yasuyuki; Kheirandish, Leila; Gozal, David; Kaplan, Henry J; McCall, Maureen A

    2006-03-01

    We characterized changes in the visual behavior of mice in which a loss of the retinal pigment epithelium (RPE) was experimentally induced with intravenous (i.v.) administration of sodium iodate (NaIO3). We compared and correlated these changes with alterations in neural retinal structure and function. RPE loss was induced in 4-6 week old male C57BL/6 mice with an i.v. injection of 1% NaIO3 at three concentrations: 35, 50, or 70 mg/kg. At 1, 3, 7, 14, 21, and 28 days (d) as well as 6 months post injection (PI) a behavioral test was performed in previously trained mice to evaluate visual function. Eye morphology was then assessed for changes in both the RPE and neural retina. NaIO3-induced RPE degeneration was both dose and PI time dependent. Our low dose showed no effects, while our high dose caused the most damage, as did longer PI times at our intermediate dose. Using the intermediate dose, no changes were detectable in either visual behavior or retinal morphology at 1 d PI. However, at 3 d PI visual behavior became abnormal and patchy RPE cell loss was observed. From 7 d PI onward, changes in retinal morphology and visual behavior became more severe. At 6 months PI, no recovery was seen in any of these measures in mice administered the intermediate dose. These results show that NaIO3 dosage and/or time PI can be varied to produce different, yet permanent deficits in retinal morphology and visual function. Thus, this approach should provide a unique system in which the onset and severity of RPE damage, and its consequences can be manipulated. As such, it should be useful in the assessment of rescue or mitigating effects of retinal or stem cell transplantation on visual function.

  16. Iodoacetic acid, but not sodium iodate, creates an inducible swine model of photoreceptor damage.

    Science.gov (United States)

    Noel, Jennifer M; Fernandez de Castro, Juan P; Demarco, Paul J; Franco, Luisa M; Wang, Wei; Vukmanic, Eric V; Peng, Xiaoyan; Sandell, Julie H; Scott, Patrick A; Kaplan, Henry J; McCall, Maureen A

    2012-04-01

    Our purpose was to find a method to create a large animal model of inducible photoreceptor damage. To this end, we tested in domestic swine the efficacy of two chemical toxins, known to create photoreceptor damage in other species: Iodoacetic Acid (IAA) and Sodium Iodate (NaIO(3)). Intravenous (IV) administration of NaIO(3) up to 90 mg/kg had no effect on retinal function and 110 mg/kg was lethal. IV administration of IAA (5-20 mg/kg) produced concentration-dependent changes in visual function as measured by full-field and multi-focal electroretinograms (ffERG and mfERG), and 30 mg/kg IAA was lethal. The IAA-induced effects measured at two weeks were stable through eight weeks post-injection, the last time point investigated. IAA at 7.5, 10, and 12 mg/kg produce a concentration-dependent reduction in both ffERG b-wave and mfERG N1-P1 amplitudes compared to baseline at all post-injection times. Comparisons of dark- and light-adapted ffERG b-wave amplitudes show a more significant loss of rod relative to cone function. The fundus of swine treated with ≥10 mg/kg IAA was abnormal with thinner retinal vessels and pale optic discs, and we found no evidence of bone spicule formation. Histological evaluations show concentration-dependent outer retinal damage that correlates with functional changes. We conclude that NaIO(3,) is not an effective toxin in swine. In contrast, IAA can be used to create a rapidly inducible, selective, stable and concentration-dependent model of photoreceptor damage in swine retina. Because of these attributes this large animal model of controlled photoreceptor damage should be useful in the investigation of treatments to replace damaged photoreceptors. Copyright © 2012 Elsevier Ltd. All rights reserved.

  17. Course of Sodium Iodate-Induced Retinal Degeneration in Albino and Pigmented Mice.

    Science.gov (United States)

    Chowers, Guy; Cohen, Matan; Marks-Ohana, Devora; Stika, Shelly; Eijzenberg, Ayala; Banin, Eyal; Obolensky, Alexey

    2017-04-01

    To characterize the course of sodium iodate (SI)-induced retinal degeneration in young adult albino and pigmented mice. Single intraperitoneal (IP) injections of SI (25, 50, and 100 mg/kg) were performed in 7- to 8-week-old BALB/c and C57Bl/6J mice. Retinal function and structure was assessed at baseline, 24 hours, 3 days, 1, 2, 3, and 4 weeks postinjection by optokinetic tracking response, ERG, optical coherence tomography (OCT), and histologic and immunohistochemical techniques. The 50 mg/kg SI dosage was selected after dose ranging due to consistent retinal effects and lack of systemic toxicity. Time-dependent deterioration in retinal function and morphology was consistently observed between 1 and 4 weeks in all measured parameters. These include reduction of ERG responses, thinning of retinal layers as observed by OCT and histology, and loss of RPE nuclei. Immunohistochemistry revealed rapid RPE disorganization with loss of tight junctions and markedly reduced expression of RPE65 and rod opsin, accompanied by mislocalization of cone opsins. Earlier time points displayed variable results, including partial recovery of visual acuity at 1 week and supranormal ERG cone responses at 24 hours, suggesting possible limitations of early intervention and assessment in the SI model. A single IP injection of 50 mg/kg SI leads to severe RPE injury followed by vision impairment, dysfunction, and loss of photoreceptors in both BALB/c and C57Bl/6J mice. This easily induced and reproducible noninherited model may serve as a useful tool for seeking and evaluating novel therapeutic modalities for the treatment of retinal degenerations caused by primary failure of the RPE.

  18. Reactions of iodate with iodine in concentrated sulfuric acid. Formation of I(+3) and I(+1) compounds

    Science.gov (United States)

    Schmitz, Guy; Noszticzius, Zoltan; Hollo, Gabor; Wittmann, Maria; Furrow, Stanley D.

    2018-01-01

    The absorption spectra in a large range of concentrations show that the reactions of iodate with iodine in 96% sulfuric acid produce (IO)HSO4, I3+ and I5+, just like in the pure 100% acid. We discovered that, in 96% H2SO4, these reactions also produce I2O which is not formed in the pure acid. I2O is an important intermediate of reactions in diluted sulfuric acid, including the Bray-Liebhafsky reaction, but it had never been observed directly because of its very high reactivity. The equilibrium constants of the reactions producing these four compounds were determined.

  19. Sol-gel-derived carbon ceramic electrode containing 9,10-phenanthrenequinone, and its electrocatalytic activity toward iodate.

    Science.gov (United States)

    Yang, Z; Wang, P; Zhang, W; Zhu, G

    2001-10-01

    9,10-Phenanthrenequinone (PQ) supported on graphite powder by adsorption was dispersed in propyltrimethoxysilane-derived gels to yield a conductive composite which was used as electrode material to fabricate a PQ-modified carbon ceramic electrode. In this configuration, PQ acts as a catalyst, graphite powder guarantees conductivity by percolation, the silicate provides a rigid porous backbone, and the propyl groups endow hydrophobicity and thus limit the wetting region of the modified electrode. Square-wave voltammetry was exploited to investigate the pH-dependent electrochemical behavior of the composite electrode and an almost Nernstian response was obtained from pH 0.42 to 6.84. Because the chemically modified electrode can electrocatalyze the reduction of iodate in acidic aqueous solution (pH 2.45), it was used as an amperometric sensor for the determination of iodate in table salt. The advantages of the electrode are that it can be polished in the event of surface fouling, it is simple to prepare, has excellent chemical and mechanical stability, and the reproducibility of surface-renewal is good.

  20. Determination of Iodate in Food, Environmental, and Biological Samples after Solid-Phase Extraction with Ni-Al-Zr Ternary Layered Double Hydroxide as a Nanosorbent

    Directory of Open Access Journals (Sweden)

    Hossein Abdolmohammad-Zadeh

    2012-01-01

    Full Text Available Nanostructured nickel-aluminum-zirconium ternary layered double hydroxide was successfully applied as a solid-phase extraction sorbent for the separation and pre-concentration of trace levels of iodate in food, environmental and biological samples. An indirect method was used for monitoring of the extracted iodate ions. The method is based on the reaction of the iodate with iodide in acidic solution to produce iodine, which can be spectrophotometrically monitored at 352 nm. The absorbance is directly proportional to the concentration of iodate in the sample. The effect of several parameters such as pH, sample flow rate, amount of nanosorbent, elution conditions, sample volume, and coexisting ions on the recovery was investigated. In the optimum experimental conditions, the limit of detection (3s and enrichment factor were 0.12 μg mL−1 and 20, respectively. The calibration graph using the preconcentration system was linear in the range of 0.2–2.8 μg mL−1 with a correlation coefficient of 0.998. In order to validate the presented method, a certified reference material, NIST SRM 1549, was also analyzed.

  1. Synthesis and characterization of f-element iodate architectures with variable dimensionality, alpha- and beta-Am(IO3)3.

    Science.gov (United States)

    Runde, Wolfgang; Bean, Amanda C; Brodnax, Lia F; Scott, Brian L

    2006-03-20

    Two americium(III) iodates, beta-Am(IO3)3 (I) and alpha-Am(IO3)3 (II), have been prepared from the aqueous reactions of Am(III) with KIO(4) at 180 degrees C and have been characterized by single-crystal X-ray diffraction, diffuse reflectance, and Raman spectroscopy. The alpha-form is consistent with the known structure type I of anhydrous lanthanide iodates. It consists of a three-dimensional network of pyramidal iodate groups bridging [AmO8] polyhedra where each of the americium ions are coordinated to eight iodate ligands. The beta-form reveals a novel architecture that is unknown within the f-element iodate series. beta-Am(IO3)3 exhibits a two-dimensional layered structure with nine-coordinate Am(III) atoms. Three crystallographically unique pyramidal iodate anions link the Am atoms into corrugated sheets that interact with one another through intermolecular IO3-...IO3- interactions forming dimeric I2O10 units. One of these anions utilizes all three O atoms to simultaneously bridge three Am atoms. The other two iodate ligands bridge only two Am atoms and have one terminal O atom. In contrast to alpha-Am(IO3)3, where the [IO3] ligands are solely corner-sharing with [AmO8] polyhedra, a complex arrangement of corner- and edge-sharing mu2- and mu3-[IO3] pyramids can be found in beta-Am(IO3)3. Crystallographic data: I, monoclinic, space group P2(1)/n, a = 8.871(3) A, b = 5.933(2) A, c = 15.315(4) A, beta = 96.948(4) degrees , V = 800.1(4) A(3), Z = 4; II, monoclinic, space group P2(1)/c, a = 7.243(2) A, b = 8.538(3) A, c = 13.513(5) A, beta = 100.123(6) degrees , V = 822.7(5) A(3), Z = 4.

  2. Synthesis, crystal structure and optical properties of two new layered cadmium iodates: Cd(IO3)X (X=Cl, OH)

    International Nuclear Information System (INIS)

    Yang, Bing-Ping; Mao, Jiang-Gao

    2014-01-01

    Systematic explorations of new compounds in the cadmium iodate system by hydrothermal reactions led to two layered iodates, namely, Cd(IO 3 )X (X=Cl, OH). Cd(IO 3 )Cl crystallizes in the orthorhombic space group Cmca (No. 64) whereas Cd(IO 3 )(OH) crystallizes in the orthorhombic space group Pnma (No. 62). Cd(IO 3 )Cl displays a unique double layered structure composed of 1 ∞ [Cd−O 3 Cl] n chains. Cadmium octahedrons form a 1D chain along the a-axis through edge sharing, and such chains are further interconnected via IO 3 groups to form a special double layer on (020) plane. Cd(IO 3 )(OH) also exhibits a layered structure that is composed of cadmium cations, IO 3 groups and hydroxyl ions. Within a layer, chains of CdO 6 edge-shared octahedra are observed along the b-axis. And these chains are connected by IO 3 groups into a layer parallel to the bc plane. Spectroscopic characterizations, elemental analysis, and thermogravimetric analysis for the reported two compounds are also presented. - Graphical abstract: Two new layered cadmium iodates Cd(IO 3 )X (X=Cl, OH) are reported. Cd(IO 3 )Cl features a unique double layered structure whereas Cd(IO 3 )(OH) displays an ordinary layered structure. - Highlights: • Two new layered cadmium iodates Cd(IO 3 )X (X=Cl, OH) are reported. • Cd(IO 3 )Cl features a unique double layered structure. • Cd(IO 3 )(OH) displays an ordinary layered structure. • The spectroscopic and thermal properties have been studied in detail

  3. Synthesis and characterization of polyacrylamide zirconium (IV iodate ion-exchanger: Its application for selective removal of lead (II from wastewater

    Directory of Open Access Journals (Sweden)

    Nafisur Rahman

    2017-05-01

    Full Text Available Polyacrylamide zirconium (IV iodate was synthesized using the sol–gel technique. The synthesis conditions such as reactant concentrations and temperature were changed to optimize the ion exchange properties of the hybrid organic–inorganic ion exchange material. Zirconium oxychloride (0.1 M was added to 0.1 M potassium iodate in the presence of 0.4 M acrylamide and heated at 70 °C for 6 h to yield the polyacrylamide zirconium (IV iodate with maximum capacity. The ion exchange capacity was found to be 3.27 meq/g for Pb(II. The hybrid material has been characterized on the basis of chemical composition FTIR, XRD, TGA-DTA, SEM and EDX studies. Sorption studies showed that the hybrid cation exchanger has a high selectivity to Pb(II in comparison to other metal ions. Its selectivity was evaluated by performing some important binary separations like Hg(II–Pb(II, Cu(II–Pb(II, Ni(II–Pb(II, Fe(III–Pb(II and Cd(II–Pb(II. In addition, the selective separation of Pb(II was also achieved from a synthetic mixture containing a large number of metal ions with a recovery of ∼98.5%. The proposed method was successfully applied for the selective removal of Pb(II from wastewater samples.

  4. Importance of Microbial Activity On Groundwater Iodate and Organo-Iodine Speciation and Mobility At Two DOE Sites

    Energy Technology Data Exchange (ETDEWEB)

    Santschi, Peter H. [Texas A & M Univ., College Station, TX (United States); Xu, Chen [Texas A & M Univ., College Station, TX (United States); Schwehr, Kathleen A. [Texas A & M Univ., College Station, TX (United States); Kaplan, Daniel I. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Yeager, Chris M. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2016-03-01

    Iodine (I) occurs in multiple oxidation states in aquatic systems in the form of organic and inorganic species (iodide and iodate). This fact leads to complex biogeochemical cycling of Iodine and its long-lived isotope, 129I, a major by-product of nuclear fission. Results from our newly developed, sensitive and rapid method for speciated isotopic ratios (129I/127I) via GC-MS, which compare favorably with Accelerator Mass Spectroscopy, demonstrate that the mobility of 129I species greatly depends on the type of I species and its concentration, pH, and sediment redox state. At ambient concentrations (~107 M), I- and IO-3 are significantly retarded by sorption to mineral surfaces and covalent binding to aromatic moieties in natural organic matter (NOM), even when NOM is present at low concentrations such as occur at Hanford. At concentrations traditionally examined in sorption studies (≥ 10-4 M), I- travels along with the water. Iodate removal can also occur through incorporation into CaCO3 crystal lattice, e.g., at the Hanford Site. Removal of iodine from the groundwater through interaction with NOM is complicated by the release of mobile organo-I species, as was observed at SRS and Hanford. A small fraction of NOM that is bound to iodine can behave as a mobile organo-I source, a process that we were able to numerically simulate. Field and laboratory studies evaluating the cause for steady increases in 129I concentrations (up to 1000 pCi L-1) emanating from radiological basins at SRS indicate that an increase of 0.7 pH units in groundwater over 17 years can account for the observed increased groundwater 129I concentrations. Bacteria from a 129I-contaminated aerobic aquifer at the F-area of SRS can accumulate I- at environmentally relevant concentrations (10-7 M), and enzymatically oxidize I-, which together with microbially produced Mn

  5. The biogeochemical effect of seaweeds upon close-to natural concentrations of dissolved iodate and iodide in seawater Preliminary study with Laminaria digitata and Fucus serratus

    Science.gov (United States)

    Truesdale, Victor W.

    2008-06-01

    Toward assessing the biogeochemical significance of seaweeds in relation to dissolved iodine in seawater, the effect of whole seaweeds ( Laminaria digitata and Fucus serratus) upon iodide and iodate, at essentially natural concentrations, has been studied. The weeds were carefully removed from the sub-littoral zone of the Menai Straits and exposed to iodide and iodate at their natural temperature (6 °C), but under continuous illumination. Laminaria digitata was found to decrease the concentration of iodate with an exponential rate constant of 0.008-0.24 h -1. This is a newly discovered process which, if substantiated, will require an entirely new mechanism. Generally, apparent iodide concentration increased except in a run with seawater augmented with iodide, where it first decreased. The rate constant for loss of iodide was 0.014-0.16 h -1. Meanwhile, F. serratus was found not to decrease iodate concentrations, as did L. digitata. Indeed, after ˜30 h iodate concentrations increased, suggesting that the weed may take in iodide before oxidising and releasing it. If substantiated, this finding may offer a way into one of the most elusive of processes within the iodine cycle - iodide oxidation. With both seaweeds sustained long-term increases of apparent iodide concentration are most easily explained as a secretion by the weeds of organic matter which is capable of reducing the Ce(IV) reagent used in determination of total iodine. Modelling of the catalytic method used is provided to support this contention. The possibility of developing this to measure the strain that seaweeds endure in this kind of biogeochemical flux experiment is discussed. A Chemical Oxygen Demand type of approach is applied using Ce(IV) as oxidant. The results of the iodine experiments are contrasted with the several investigations of 131I interaction with seaweeds, which have routinely used discs of weed cut from the frond. It is argued that experiments conducted with stable iodine may

  6. Acentric La3(IO3)8(OH) and La(IO3)2(NO3): Partial Substitution of Iodate Anions in La(IO3)3 by Hydroxide or Nitrate Anion.

    Science.gov (United States)

    Mao, Fei-Fei; Hu, Chun-Li; Li, Bing-Xuan; Mao, Jiang-Gao

    2017-11-20

    Partial substitution of iodate anions in La(IO 3 ) 3 by OH - or NO 3 - anion led to acentric La 3 (IO 3 ) 8 (OH) and chiral La(IO 3 ) 2 (NO 3 ). The structure of La 3 (IO 3 ) 8 (OH) can be seen as a complex three-dimensional (3D) network composed of two-dimensional [La 3 (IO 3 ) 2 (OH)] 6+ cationic layers that are further bridged by remaining iodate anions, or alternatively as a 3D network composed of one-dimensional [La 3 (IO 3 ) 6 (OH)] 2+ cationic columns being further interconnected by additional iodate anions, while the structure of La(IO 3 ) 2 (NO 3 ) can be seen as a novel 3D structure with planar NO 3 groups serving as linkage between the [La 3 (IO 3 ) 6 ] 3+ triple layers. Compared to La(IO 3 ) 3 , both compounds show considerably wide band gaps and enhanced thermal stability. La(IO 3 ) 2 (NO 3 ) shows a moderate second harmonic generation (SHG) response of ∼0.6 times that of KDP (KH 2 PO 4 ), a wide band gap of 4.23 eV, and a high LDT value (22 × AgGaS 2 ). Optical property measurements, thermal analysis, as well as theoretical calculations on SHG origin, were performed. It can be deduced that partial substitution of iodate anions can be a facile route to design new noncentrosymmetric metal iodates with novel structure and potential application.

  7. Retinal Cell Death Caused by Sodium Iodate Involves Multiple Caspase-Dependent and Caspase-Independent Cell-Death Pathways

    Directory of Open Access Journals (Sweden)

    Jasmin Balmer

    2015-07-01

    Full Text Available Herein, we have investigated retinal cell-death pathways in response to the retina toxin sodium iodate (NaIO3 both in vivo and in vitro. C57/BL6 mice were treated with a single intravenous injection of NaIO3 (35 mg/kg. Morphological changes in the retina post NaIO3 injection in comparison to untreated controls were assessed using electron microscopy. Cell death was determined by TdT-mediated dUTP-biotin nick end labeling (TUNEL staining. The activation of caspases and calpain was measured using immunohistochemistry. Additionally, cytotoxicity and apoptosis in retinal pigment epithelial (RPE cells, primary retinal cells, and the cone photoreceptor (PRC cell line 661W were assessed in vitro after NaIO3 treatment using the ApoToxGlo™ assay. The 7-AAD/Annexin-V staining was performed and necrostatin (Nec-1 was administered to the NaIO3-treated cells to confirm the results. In vivo, degenerating RPE cells displayed a rounded shape and retracted microvilli, whereas PRCs featured apoptotic nuclei. Caspase and calpain activity was significantly upregulated in retinal sections and protein samples from NaIO3-treated animals. In vitro, NaIO3 induced necrosis in RPE cells and apoptosis in PRCs. Furthermore, Nec-1 significantly decreased NaIO3-induced RPE cell death, but had no rescue effect on treated PRCs. In summary, several different cell-death pathways are activated in retinal cells as a result of NaIO3.

  8. Modification of glassy carbon electrode with multi-walled carbon nanotubes and iron(III)-porphyrin film: Application to chlorate, bromate and iodate detection

    International Nuclear Information System (INIS)

    Salimi, Abdollah; MamKhezri, Hussein; Hallaj, Rahman; Zandi, Shiva

    2007-01-01

    In this study, multi-wall carbon nanotubes (MWCTs) is evaluated as a transducer, stabilizer and immobilization matrix for the construction of amperometric sensor based on iron-porphyrin. 5,10,15,20-Tetraphenyl-21H,23H-porphine iron(III) chloride (Fe(III)P) adsorbed on MWCNTs immobilized on the surface of glassy carbon electrode. Cyclic voltammograms of the Fe(III)P-incorporated-MWCNTs indicate a pair of well-defined and nearly reversible redox couple with surface confined characteristics at wide pH range (2-12). The surface coverage (Γ) and charge transfer rate constant (k s ) of Fe(III)P immobilized on MWCNTs were 7.68 x 10 -9 mol cm -2 and 1.8 s -1 , respectively, indicating high loading ability of MWCNTs for Fe(III)P and great facilitation of the electron transfer between Fe(III)P and carbon nanotubes immobilized on the electrode surface. Modified electrodes exhibit excellent electrocatalytic activity toward reduction of ClO 3 - , IO 3 - and BrO 3 - in acidic solutions. The catalytic rate constants for catalytic reduction of bromate, chlorate and iodate were 6.8 x 10 3 , 7.4 x 10 3 and 4.8 x 10 2 M -1 s -1 , respectively. The hydrodynamic amperometry of rotating-modified electrode at constant potential versus reference electrode was used for detection of bromate, chlorate and iodate. The detection limit, linear calibration range and sensitivity for chlorate, bromate and iodate detections were 0.5 μM, 2 μM to 1 mM, 8.4 nA/μM, 0.6 μM, 2 μM to 0.15 mM, 11 nA/μM, and 2.5 μM, 10 μM to 4 mM and 1.5 nA/μM, respectively. Excellent electrochemical reversibility of the redox couple, good reproducibility, high stability, low detection limit, long life time, fast amperometric response time, wide linear concentration range, technical simplicity and possibility of rapid preparation are great advantages of this sensor. The obtained results show promising practical application of the Fe(III)P-MWCNTs-modified electrode as an amperometric sensor for chlorate, iodate and

  9. A Highly Sensitive and Selective Method for the Determination of an Iodate in Table-salt Samples Using Malachite Green-based Spectrophotometry.

    Science.gov (United States)

    Konkayan, Mongkol; Limchoowong, Nunticha; Sricharoen, Phitchan; Chanthai, Saksit

    2016-01-01

    A simple, rapid, and sensitive malachite green-based spectrophotometric method for the selective trace determination of an iodate has been developed and presented for the first time. The reaction mixture was specifically involved in the liberation of iodine in the presence of an excess of iodide in an acidic condition following an instantaneous reaction between the liberated iodine and malachite green dye. The optimum condition was obtained with a buffer solution pH of 5.2 in the presence of 40 mg L -1 potassium iodide and 1.5 × 10 -5 M malachite green for a 5-min incubation time. The iodate contents in some table-salt samples were in the range of 26 to 45 mg kg -1 , while those of drinking water, tap water, canal water, and seawater samples were not detectable (< 96 ng mL -1 of limits of detection, LOQ) with their satisfied method of recoveries of between 93 and 108%. The results agreed with those obtained using ICP-OES for comparison.

  10. Magnetism and Raman spectroscopy of the dimeric lanthanide iodates Ln(IO3)3 (Ln=Gd, Er) and magnetism of Yb(IO3)3

    International Nuclear Information System (INIS)

    Sykora, Richard E.; Khalifah, Peter; Assefa, Zerihun; Albrecht-Schmitt, Thomas E.; Haire, Richard G.

    2008-01-01

    Colorless single crystals of Gd(IO 3 ) 3 or pale pink single crystals of Er(IO 3 ) 3 have been formed from the reaction of Gd metal with H 5 IO 6 or Er metal with H 5 IO 6 under hydrothermal reaction conditions at 180 deg. C. The structures of both materials adopt the Bi(IO 3 ) 3 structure type. Crystallographic data are (MoKα, λ=0.71073 A): Gd(IO 3 ) 3 , monoclinic, space group P2 1 /n, a=8.7615(3) A, b=5.9081(2) A, c=15.1232(6) A, β=96.980(1) o , V=777.03(5) Z=4, R(F)=1.68% for 119 parameters with 1930 reflections with I>2σ(I); Er(IO 3 ) 3 , monoclinic, space group P2 1 /n, a=8.6885(7) A, b=5.9538(5) A, c=14.9664(12) A, β=97.054(1) o , V=768.4(1) Z=4, R(F)=2.26% for 119 parameters with 1894 reflections with I>2σ(I). In addition to structural studies, Gd(IO 3 ) 3 , Er(IO 3 ) 3 , and the isostructural Yb(IO 3 ) 3 were also characterized by Raman spectroscopy and magnetic property measurements. The results of the Raman studies indicated that the vibrational profiles are adequately sensitive to distinguish between the structures of the iodates reported here and other lanthanide iodate systems. The magnetic measurements indicate that only in Gd(IO 3 ) 3 did the 3+ lanthanide ion exhibit its full 7.9 μ B Hund's rule moment; Er 3+ and Yb 3+ exhibited ground state moments and gap energy scales of 8.3 μ B /70 K and 3.8 μ B /160 K, respectively. Er(IO 3 ) 3 exhibited extremely weak ferromagnetic correlations (+0.4 K), while the magnetic ions in Gd(IO 3 ) 3 and Yb(IO 3 ) 3 were fully non-interacting within the resolution of our measurements (∼0.2 K). - Graphical abstract: Three f-element iodates Ln(IO 3 ) 3 (Ln=Gd, Er, Yb), all containing the Bi(IO 3 ) 3 structure type, were characterized by Raman spectroscopy and magnetic property measurements. The results of the Raman studies indicated that the vibrational profiles are adequately sensitive to distinguish between the structures of the iodates reported here and other lanthanide iodate systems. The magnetic

  11. The effects of dietary calcium iodate on productive performance, egg quality and iodine accumulation in eggs of laying hens.

    Science.gov (United States)

    Bakhshalinejad, R; Hassanabadi, A; Nassiri-Moghaddam, H; Zarghi, H

    2018-01-25

    The aim of this study was to examine the effects of various levels of supplemental calcium iodate (CI) on productive performance, egg quality, blood indices and iodine (I) accumulation in the eggs in commercial laying hens. A total of 240 White Leghorn layers (Hy-line W36) were divided through a completely randomized design into six treatments with five replicates and eight hens per each at 32 weeks of age. This experiment lasted for 12 weeks. Concentrations of I in the mash diets were 0.74, 3.13, 5.57, 8.11, 10.65 and 12.94 mg I/kg of feed in treatments 1-6 respectively. The added doses of CI were included 0.0 (control), 2.5, 5.0, 7.5, 10.0 and 12.5 mg/kg of diet for treatments 1-6 respectively. There were no significant differences in productive performance among the treatments. The highest eggshell strength was observed in group fed diet containing 3.13 mg I/kg (p = .014). The highest percentage of calcium and lowest percentage of phosphorus in eggshell were observed in group fed diet containing 12.94 mg I/kg (p = .0001). Feeding hens with diet containing 12.94 mg I/kg increased serum triiodothyronine-to-thyroxine ratio (p = .0001). Serum alanine aminotransferase activity in hens fed diet containing 12.94 mg I/kg was significantly more than control (p = .041). Blood Serum triglycerides in hens fed diet containing 8.11 mg I/kg were significantly higher than control (p = .0001). Edible fraction of the eggs of birds fed diet containing 12.94 mg I/kg was enriched by I almost 3 times more than those fed diet containing 0.74 mg I/kg. The results suggested that egg production, egg mass, feed intake and feed conversion ratio were not significantly affected by dietary I levels. Iodine accumulation in the eggs were increased by increasing dietary I levels and the level of 10 mg/kg CI could supply I enrichment of the eggs. © 2018 Blackwell Verlag GmbH.

  12. Polarographic determination of Iodide and Iodate, in Solutions Coming from Aerosols in Fission Products Containment Studies in Nuclear Power Stations; Determinacion Polarografica de Especies de Iodo (Ioduro y Iodato) en Soluciones Procedentes de Aerosoles, para Estudios de Contencion de Productos de Fision en Centrales Nucleares

    Energy Technology Data Exchange (ETDEWEB)

    Sanchez, M.; Ballesteros, O.; Fernandez, M.; Clavero, M.; Gonzalez, A. M. [Ciemat, Madrid (Spain)

    2000-07-01

    A polarographic method is described for the iodine species determination, iodide and iodate in water solutions. the iodate can be determined by differential pulse polarography. Calibration curves and the detection and determination limits have been obtained. Iodides is oxidized to iodate with sodium hypochlorite and the excess of oxidizing agent is destroyed with sodium sulphide. The concentration of iodide is calculated as the difference between the concentration of iodate in the sample before and after the oxidation. As an application, species of iodine in samples coming from the experimental plants GIRS (Gaseous Iodine Removal by Sprays) of Nuclear Fission Department of the CIEMAT, dedicated to fission products containment studies in nuclear power station, were determined. (Author) 10 refs.

  13. Differential determination of trace amounts of iodide and iodate in water by solvent extraction-inductively coupled plasma atomic emission spectrometry

    International Nuclear Information System (INIS)

    Miyazaki, Akira; Bansho, Kenji

    1987-01-01

    Inductively coupled plasma-atomic emission spectrometry (ICP-AES) combined with solvent extraction has been investigated to determine trace amounts of iodide and iodate in water. Nonpolar solvents such as nonane and decane show higher signal-to-background ratios than the polar solvents such as xylene and diisobutyl ketone (DIBK). However, memory effects in the nebulizer spray chamber are severe. This phenomenon is discussed in relation to the characteristics of iodine such as the formation of the charge transfer complex and the solubility in the organic solvents. The detection limits at 178.28 and 206.16 nm for the original samples (concentration factor = 50) obtained by using xylene as the extractant are 8.3 and 21 ng ml -1 of I, respectively. By the back extraction of iodine from xylene into 0.5% ascorbic acid solution, the detection limit (concentration factor = 100) at 178.28 nm is improved to 1.6 ng ml -1 . Most other ions except for the large amounts of bromide do not interfere. This method is applied to the analysis of brines and coastal seawaters. (author)

  14. Dimensionality variations in new zirconium iodates: hydrothermal syntheses, structural determination, and characterization of BaZr(IO₃)₆ and K₂Zr(IO₃)₆.

    Science.gov (United States)

    Ahn, Hyun Sun; Lee, Dong Woo; Ok, Kang Min

    2014-07-21

    Two new quaternary zirconium iodates, BaZr(IO3)6 and K2Zr(IO3)6, have been synthesized through hydrothermal reactions using BaCO3 (or K2CO3), ZrO2, and HIO3 as reagents. Single crystal and powder X-ray diffraction were used to determine crystal structures of the compounds. BaZr(IO3)6 exhibits infinite bands that are composed of ZrO7 pentagonal bipyramids and IO3 trigonal pyramids, in which Ba(2+) cations are sandwiched by the bands. K2Zr(IO3)6 exhibits a molecular structure that is composed of ZrO6 octahedra and IO3 groups. The dimensionality variations seem to be attributable to the flexible coordination numbers of Zr(4+) cations with large ionic radii as well as the number of counter cations. Both of the materials are thermally stable up to approximately 440-450 °C and decompose to the corresponding metal zirconium oxides above these temperatures. The band gaps for BaZr(IO3)6 and K2Zr(IO3)6 are calculated to be 3.1 and 3.0 eV, respectively, using the (K/S)-versus-E plots obtained from the UV-vis diffuse reflectance spectra. Infrared spectra and local dipole moment calculations are also presented.

  15. Electrosorption of Os(III)-complex at single-wall carbon nanotubes immobilized on a glassy carbon electrode: Application to nanomolar detection of bromate, periodate and iodate

    International Nuclear Information System (INIS)

    Salimi, Abdollah; Kavosi, Begard; Babaei, Ali; Hallaj, Rahman

    2008-01-01

    A simple procedure was developed to prepare a glassy carbon electrode modified with single-wall carbon nanotubes (SWCNTs) and Os(III)-complex. The glassy carbon (GC) electrode modified with CNTs was immersed into Os(III)-complex solution (direct deposition) for a short period of time (60 s). 1,4,8,12-Tetraazacyclotetradecane osmium(III) chloride, (Os(III)LCl 2 ).ClO 4 , irreversibly and strongly adsorbed on SWCNTs immobilized on the surface of GC electrode. Cyclic voltammograms of the Os(III)-complex-incorporated-SWCNTs indicate a pair of well defined and nearly reversible redox couple with surface confined characteristic at wide pH range (1-8). The surface coverage (Γ) and charge transfer rate constant (k s ) of the immobilized Os-complex on SWCNTs were 3.07 x 10 -9 mol cm -2 , 5.5 (±0.2) s -1 , 2.94 x 10 -9 mol cm -2 , 7.3 (±0.3) s -1 at buffer solution with pH 2 and 7, respectively, indicate high loading ability of SWCNTs for Os(III) complex and great facilitation of the electron transfer between electroactive redox center and carbon nanotubes immobilized on the electrode surface. Modified electrodes showed higher electrocatalytic activity toward reduction of BrO 3 - , IO 3 - and IO 4 - in acidic solutions. The catalytic rate constants for catalytic reduction bromate, periodate and iodate were 3.79 (±0.2) x 10 3 , 7.32 (±0.2) x 10 3 and 1.75 (±0.2) x 10 3 M -1 s -1 , respectively. The hydrodynamic amperometry of rotating modified electrode at constant potential (0.3 V) was used for nanomolar detection of selected analytes. Excellent electrochemical reversibility of the redox couple, good reproducibility, high stability, low detection limit, long life time, fast amperometric response time, wide linear concentration range, technical simplicity and possibility of rapid preparation are great advantage of this sensor

  16. Syntheses, structures, and vibrational spectroscopy of the two-dimensional iodates Ln(IO3)3 and Ln(IO3)3(H2O) (Ln =Yb, Lu)

    International Nuclear Information System (INIS)

    Assefa, Zerihun; Ling Jie; Haire, Richard G.; Albrecht-Schmitt, Thomas E.; Sykora, Richard E.

    2006-01-01

    The reaction of Lu 3+ or Yb 3+ and H 5 IO 6 in aqueous media at 180 o C leads to the formation of Yb(IO 3 ) 3 (H 2 O) or Lu(IO 3 ) 3 (H 2 O), respectively, while the reaction of Yb metal with H 5 IO 6 under similar reaction conditions gives rise to the anhydrous iodate, Yb(IO 3 ) 3 . Under supercritical conditions Lu 3+ reacts with HIO 3 and KIO 4 to yield the isostructural Lu(IO 3 ) 3 . The structures have been determined by single-crystal X-ray diffraction. Crystallographic data are (MoKα, λ=0.71073 A): Yb(IO 3 ) 3 , monoclinic, space group P2 1 /n, a=8.6664(9) A, b=5.9904(6) A, c=14.8826(15) A, β=96.931(2) o , V=766.99(13), Z=4, R(F)=4.23% for 114 parameters with 1880 reflections with I>2σ(I); Lu(IO 3 ) 3 , monoclinic, space group P2 1 /n, a=8.6410(9), b=5.9961(6), c=14.8782(16) A, β=97.028(2) o , V=765.08(14), Z=4, R(F)=2.65% for 119 parameters with 1756 reflections with I>2σ(I); Yb(IO 3 ) 3 (H 2 O), monoclinic, space group C2/c, a=27.2476(15), b=5.6296(3), c=12.0157(7) A, β=98.636(1) o , V=1822.2(2), Z=8, R(F)=1.51% for 128 parameters with 2250 reflections with I>2σ(I); Lu(IO 3 ) 3 (H 2 O), monoclinic, space group C2/c, a=27.258(4), b=5.6251(7), c=12.0006(16) A, β=98.704(2) o , V=1818.8(4), Z=8, R(F)=1.98% for 128 parameters with 2242 reflections with I>2σ(I). The f elements in all of the compounds are found in seven-coordinate environments and bridged with monodentate, bidentate, or tridentate iodate anions. Both Lu(IO 3 ) 3 (H 2 O) and Yb(IO 3 ) 3 (H 2 O) display distinctively different vibrational profiles from their respective anhydrous analogs. Hence, the Raman profile can be used as a complementary diagnostic tool to discern the different structural motifs of the compounds. - Graphical abstract: Four new metal iodates, Yb(IO 3 ) 3 , Lu(IO 3 ) 3 , Yb(IO 3 ) 3 (H 2 O), and Lu(IO 3 ) 3 (H 2 O), have all been isolated as single crystals through the use of hydrothermal reactions. Structural determinations using single-crystal X-ray diffraction have

  17. Mixed-metal uranium(VI) iodates: hydrothermal syntheses, structures, and reactivity of Rb[UO(2)(CrO(4))(IO(3))(H(2)O)], A(2)[UO(2)(CrO(4))(IO(3))(2)] (A = K, Rb, Cs), and K(2)[UO(2)(MoO(4))(IO(3))(2)].

    Science.gov (United States)

    Sykora, Richard E; McDaniel, Steven M; Wells, Daniel M; Albrecht-Schmitt, Thomas E

    2002-10-07

    The reactions of the molecular transition metal iodates A[CrO(3)(IO(3))] (A = K, Rb, Cs) with UO(3) under mild hydrothermal conditions provide access to four new, one-dimensional, uranyl chromatoiodates, Rb[UO(2)(CrO(4))(IO(3))(H(2)O)] (1) and A(2)[UO(2)(CrO(4))(IO(3))(2)] (A = K (2), Rb (3), Cs (4)). Under basic conditions, MoO(3), UO(3), and KIO(4) can be reacted to form K(2)[UO(2)(MoO(4))(IO(3))(2)] (5), which is isostructural with 2 and 3. The structure of 1 consists of one-dimensional[UO(2)(CrO(4))(IO(3))(H(2)O)](-) ribbons that contain uranyl moieties bound by bridging chromate and iodate anions as well as a terminal water molecule to create [UO(7)] pentagonal bipyramidal environments around the U(VI) centers. These ribbons are separated from one another by Rb(+) cations. When the iodate content is increased in the hydrothermal reactions, the terminal water molecule is replaced by a monodentate iodate anion to yield 2-4. These ribbons can be further modified by replacing tetrahedral chromate anions with MoO(4)(2)(-) anions to yield isostructural, one-dimensional [UO(2)(MoO(4))(IO(3))(2)](2)(-) ribbons. Crystallographic data: 1, triclinic, space group P(-)1, a = 7.3133(5) A, b = 8.0561(6) A, c = 8.4870(6) A, alpha = 88.740(1) degrees, beta = 87.075(1) degrees, gamma = 71.672(1) degrees, Z = 2; 2, monoclinic, space group P2(1)/c, a = 11.1337(5) A, b = 7.2884(4) A, c = 15.5661(7) A, beta = 107.977(1) degrees, Z = 4; 3, monoclinic, space group P2(1)/c, a = 11.3463(6) A, b = 7.3263(4) A, c = 15.9332(8) A, beta = 108.173(1) degrees, Z = 4; 4, monoclinic, space group P2(1)/n, a = 7.3929(5) A, b = 8.1346(6) A, c = 22.126(2) A, beta = 90.647(1) degrees, Z = 4; 5, monoclinic, space group P2(1)/c, a = 11.3717(6) A, b = 7.2903(4) A, c = 15.7122(8) A, beta = 108.167(1) degrees, Z = 4.

  18. 21 CFR 184.1206 - Calcium iodate.

    Science.gov (United States)

    2010-04-01

    ... CONSUMPTION (CONTINUED) DIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE Listing of Specific... defined in § 170.3(o)(6) of this chapter. (d) The ingredient is used in the manufacture of bread in...

  19. 21 CFR 184.1635 - Potassium iodate.

    Science.gov (United States)

    2010-04-01

    ... HUMAN CONSUMPTION (CONTINUED) DIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE Listing of... used in the manufacture of bread in accordance with § 184.1(b)(2) of this chapter in an amount not to...

  20. A Facile Spectrophotometric Method for the Determination of Iodate ...

    African Journals Online (AJOL)

    NJD

    2006-12-06

    Dec 6, 2006 ... 8 V. Olgasi, P. Hedrich, J. Marta, D.P. Dejan, Glas. Hem. Drus, Beugrad,. 1971, 44, 567–569. 9 Y.M. Temerk, M.E. Ahmed and M.M. Kamal, Fresenius J. Anal Chim.,. 1980, 30, 414–417. 10 A.F. Gutierrez, A.M. Pena and J.A. Murillo, Anal. Lett., 1983, 16,. 759–762. 11 J.H. Mendez, M.A. Alonso, A. Parra, M.J. ...

  1. Determination of Iodates using Silver Solid Amalgam Electrodes

    Czech Academy of Sciences Publication Activity Database

    Josypčuk, Bohdan; Novotný, Ladislav

    2002-01-01

    Roč. 14, 15/16 (2002), s. 1138-1142 ISSN 1040-0397 R&D Projects: GA ČR GV204/97/K084 Institutional research plan: CEZ:AV0Z4040901 Keywords : silver solid amalgam electrodes * voltammetry * table salt Subject RIV: CG - Electrochemistry Impact factor: 1.783, year: 2002

  2. Effects of Potassium Iodate Application on the Biomass and Iodine ...

    African Journals Online (AJOL)

    Iodine is a trace element in soil and water that is involved in some important metabolic functions in human development. In many areas of the world, the surface soil becomes progressively poorer in iodide through accelerated deforestation, flooding and soil erosion. Hence, the food grown in iodine deficient regions can ...

  3. Behaviour of iodide, iodate and periodate in TLC with alcohol-aqueous ammonia eluent

    International Nuclear Information System (INIS)

    Benes, J.

    1979-01-01

    The behaviour of I - , IO 3 - and IO 4 - in silica gel thin layer chromatography and their separation with ammonia-alcohol eluents (saturated open-chain C1 to C5 alcohols were used) were studied using radioisotopes. Changes in Rsub(F) values of the studied anions caused by changes in the alcohol, ratio of the organic to aqueous phases in the mixture, and overall analytical concentration of ammonium ions were determined. The effect of alcohol on the kinetics of development of the chromatograms with the alcohol-water mixtures was also studied. (author)

  4. Effects of the starch indicator on the buoyantly unstable iodate-arsenous acid reaction front

    Czech Academy of Sciences Publication Activity Database

    Šebestíková, Lenka; Šimčík, Miroslav; Růžička, Marek

    2017-01-01

    Roč. 2, č. 24 (2017), s. 7141-7149 ISSN 2365-6549 R&D Projects: GA ČR GAP105/10/0919 Institutional support: RVO:67985874 ; RVO:67985858 Keywords : autocatalysis * exchange interaction * iodine * liquids * reaction mechanism Subject RIV: BK - Fluid Dynamics; CI - Industrial Chemistry, Chemical Engineering (UCHP-M) OBOR OECD: Fluids and plasma physics (including surface physics); Chemical process engineering (UCHP-M)

  5. Effects of the starch indicator on the buoyantly unstable iodate-arsenous acid reaction front

    Czech Academy of Sciences Publication Activity Database

    Šebestíková, Lenka; Šimčík, Miroslav; Růžička, Marek

    2017-01-01

    Roč. 2, č. 24 (2017), s. 7141-7149 ISSN 2365-6549 R&D Projects: GA ČR GAP105/10/0919 Institutional support: RVO:67985874 ; RVO:67985858 Keywords : autocatalysis * exchange interaction * iodine * liquids * reaction mechanism Subject RIV: BK - Fluid Dynamics ; CI - Industrial Chemistry, Chemical Engineering (UCHP-M) OBOR OECD: Fluids and plasma physics (including surface physics); Chemical process engineering (UCHP-M)

  6. Potassium iodate assisted synthesis of titanium dioxide nanoparticles with superior water-dispersibility.

    Science.gov (United States)

    Wang, Yawen; Duo, Fangfang; Peng, Shiqi; Jia, Falong; Fan, Caimei

    2014-09-15

    In this paper, we report a novel polyol process to synthesize highly water-dispersible anatase titanium dioxide (TiO2) nanoparticles (∼5 nm) by the introduction of inorganic oxidizing agent--KIO3. The obtained TiO2 nanoparticles are well dispersible in water at pH≥5.0 and the resulting aqueous dispersion remains stable over months. The superior water-dispersibility of as-formed TiO2 is ascribed to the electrostatic repulsion from carboxylic acid group modified on TiO2 nanoparticles, which is the oxidation product of solvent diethylene glycol (DEG) by KIO3. Based on the characterization results, the formation processes of water-dispersibility TiO2 nanoparticles are proposed. Meanwhile, the synthesized TiO2 nanoparticles are found to be doped by iodine and exhibit excellent photocatalytic activity on degradation of rhodamine-B (RhB) under visible-light irradiation. The further tests demonstrate that the O(2-) is the main active species during photodegradation of RhB. Copyright © 2014 Elsevier Inc. All rights reserved.

  7. Iodide and iodate (129I and 127I) in surface water of the Baltic Sea, Kattegat and Skagerrak

    DEFF Research Database (Denmark)

    Hansen, Violeta; Yi, Peng; Hou, Xiaolin

    2011-01-01

    Despite the common incorporation of iodine in the biological cycle and occurrence of huge contamination of the radioactive isotope 129I in the Baltic Proper, Skagerrak and Kattegat, there is no data on chemical speciation of iodine in these waters. We here present first time data on iodine isotopes...

  8. Phototransformation of iodate by UV irradiation: Kinetics and iodinated trihalomethane formation during subsequent chlor(am)ination

    Energy Technology Data Exchange (ETDEWEB)

    Tian, Fu-Xiang [School of Chemical and Environmental Engineering, Shanghai Institute of Technology, Shanghai 201418 (China); Hu, Xiao-Jun, E-mail: hu-xj@mail.tsinghua.edu.cn [School of Chemical and Environmental Engineering, Shanghai Institute of Technology, Shanghai 201418 (China); Xu, Bin; Zhang, Tian-Yang; Gao, Yu-Qiong [State Key Laboratory of Pollution Control and Resources Reuse, Key Laboratory of Yangtze Water Environment, Ministry of Education, College of Environmental Science and Engineering, Tongji University, Shanghai 200092 (China)

    2017-03-15

    Highlights: • IO{sub 3}{sup −} can be photodegraded by UV irradiation with pseudo-first order kinetics. • Solution pH has no remarkable influence on the photodegradation rate of IO{sub 3}{sup −}. • The I{sup −} and HOI derived from the photoreduction of IO{sub 3}{sup −} were determined. • The presence of NOM greatly enhanced the photolysis rate of IO{sub 3}{sup −}. • NOM sources can affect the formation of I-THMs in UV-chlor(am)ination of IO{sub 3}{sup −}. - Abstract: The photodegradation of IO{sub 3}{sup −} at 254 nm and the formation of iodinated trihalomethanes (I-THMs) during subsequent chlorination or chloramination in the presence of natural organic matter (NOM) were investigated in this study. The thermodynamically stable IO{sub 3}{sup −} can be degraded by UV irradiation with pseudo-first order kinetics and the quantum yield was calculated as 0.0591 mol einstein{sup −1}. Solution pH posed no remarkable influence on the photolysis rate of IO{sub 3}{sup −}. The UV phototransformation of IO{sub 3}{sup −} was evidenced by the determination of iodide (I{sup −}) and hypoiodous acid (HOI) in solution. NOM sources not only enhanced the photodegradation rate of IO{sub 3}{sup −} by photoejecting solvated electrons, but also greatly influenced the production I-THMs in subsequent chlor(am)ination processes. In UV irradiation and sequential oxidation processes by chlorine or chloramine, the I-THMs formation was susceptible to NOM sources, especially the two major fractions of aqueous humic substances (humic acid and fulvic acid). The toxicity of disinfected waters greatly increased in chloramination over chlorination of the UV photodecomposed IO{sub 3}{sup −}, as far more I-THMs especially CHI{sub 3}, were formed. As “the fourth iodine source” of iodinated disinfection by-products, the occurrence, transportation and fate of IO{sub 3}{sup −} in aquatic environment should be of concern instead of being considered a desired iodine sink.

  9. Temperature Oscillations, Complex Oscillations, and Elimination of Extraordinary Temperature Sensitivity in the Iodate-Sulfite-Thiosulfate Flow System

    Science.gov (United States)

    Liu, Haimiao; Xie, Jingxuan; Yuan, Ling; Gao, Qingyu

    2009-09-01

    Temperature oscillations and complex pH oscillations in the IO3--SO32--S2O32- system were observed in a continuously flow stirred tank reactor. During one period of oscillation, the temperature increases rapidly while the pH shows an extremely sharp change. High-amplitude pH oscillations undergo 11 complex oscillations (LS, oscillations with L large peaks and S small peaks per period) to another kind of higher-amplitude regular oscillations upon increasing the concentration of sulfite step by step. Importantly, the longstanding experimental phenomena, the extraordinary temperature sensitivity of oscillatory behavior reported 20 years ago by Rábai and Beck, can be eliminated by premixing of sulfite and sulfuric acid before entering into the reactor, avoiding local acidification, which brings out fluctuation and temperature sensitivity. The temperature oscillations can be understood by taking into account the interaction between thermal effect of various reactions and heat transfer. Experimental observations, both temperature oscillations and 11-type pH oscillations, are reproduced with a four-step Horváth model by addition of an energy-balance equation. This new detailed dynamical behavior would have potential applications in designing complex chemical waves and pH responsive gels with rhythmical motion.

  10. Study of gel grown mixed crystals of Bax (IO3 )4

    Indian Academy of Sciences (India)

    Administrator

    Mixed iodate crystals of barium calcium iodate are used in medicine and production of other iodates. The purpose of the present paper is to report the growth and influence of various parameters such as pH of gel, gel reactants, gel concentrations, effect of neutral gel etc on the growth mechanism of mixed iodate crystals of.

  11. Effects of varying dietary iodine supplementation levels as iodide or iodate on thyroid status as well as mRNA expression and enzyme activity of antioxidative enzymes in tissues of grower/finisher pigs.

    Science.gov (United States)

    Li, Qimeng; Mair, Christiane; Schedle, Karl; Hellmayr, Isabella; Windisch, Wilhelm

    2013-02-01

    The objective of this study was to investigate the influence of high dietary iodine supply and different iodine sources on thyroid status and oxidative stress in target tissues of the thyroid hormones in fattening pigs. Eighty castrates (body weight: 33.3 ± 0.4 kg) were randomly allotted into five different treatments: The control diet contained 150 μg I/kg as KI, the other feeding groups were supplemented with 4,000 μg I/kg (as KI and KIO(3)) and 10,000 μg I/kg (as KI and KIO(3)), respectively. The mRNA expression levels of sodium/iodide symporter (NIS) and key antioxidant enzymes (Cu/Zn SOD, CAT, GPx) were analyzed in thyroid gland, liver, kidney, muscle, and adipose tissue sampled during slaughter. Furthermore, antioxidant enzyme activities and the effect on lipid peroxidation (MDA) were determined in liver and muscle. In thyroid gland, a significant downregulation of NIS and Cu/Zn SOD mRNA expression was observed in high-iodine groups. In liver, a source effect on the mRNA expression of Cu/Zn SOD between KI and KIO(3) at 4,000 μg I/kg was shown. In contrast, not SOD but GPx activity was affected by iodine source with strongest downregulation in high KIO(3) group. In muscle, GPx activity was affected by both iodine source and dose, showing stronger downregulation in KI groups. In kidney and adipose tissue, oxidative stress parameters showed no or only unsystematic changes. However, variation in iodine supply had no effect on MDA concentrations. NIS expression was significantly decreased with increased iodine supplementation, which is to ensure the thyroid gland function. However, the alleviating effect of iodine supplementation observed in antioxidant enzyme mRNA expression and activity did not reflect on the lipid peroxide level.

  12. Download this PDF file

    African Journals Online (AJOL)

    USER

    determination of iodate (IO3-) in table salt and sea water. The proposed method is based on the reaction of iodate with potassium iodide in an acid medium to liberate iodine. The liberated iodine bleaches the blue color of methylene blue and is measured at 665.6 nm. This decrease in absorbance is directly proportional to ...

  13. UJI LAPANGAN ALAT PRODUKSI GARAM BERYODIUM BERSKALA KECIL DI DAERAH GANGGUAN AKIBAT KURANG YODIUM

    Directory of Open Access Journals (Sweden)

    Hermana Hermana

    2012-11-01

    Full Text Available The problem in supplying iodine to people suffering from iodine deficiency disorders are technique to produce iodated salt and the great distance between producers and consumers. The delivery of iodine would be more effective if production of iodated salt is carried out near or in areas of iodine deficiency disorders. Nutrition Research and Development Centre, Ministry of Health, RI has produced a small-scale salt iodation plant. The plant has been tested in the laboratory. Field trial of the plant was carried out in collaboration with the Village Cooperatives Unit (Koperasi Unit Desa at Bulu Cindeo, District of Pangkajene and Kepulauan, South Sulawesi. Locally-produced salt was iodated. The product was distributed not only in Pangkep but in neighbouring districts as well. It was observed that the small scale iodation plant was an appropriate technology for village level. It could be operated by man powers having minimum education (primary school. The production unit needs a not-too-big investment to run the plant During the trial, the Cooperatives learned that the plant was efficient and was economically profitable. The availability of iodated salt in the area, resulted in increased consumption.Keywords: salt iodation, iodation machine.

  14. Copper and silver halates

    CERN Document Server

    Woolley, EM; Salomon, M

    2013-01-01

    Copper and Silver Halates is the third in a series of four volumes on inorganic metal halates. This volume presents critical evaluations and compilations for halate solubilities of the Group II metals. The solubility data included in this volume are those for the five compounds, copper chlorate and iodate, and silver chlorate, bromate and iodate.

  15. SPECTROPHOTOMETRIC METHOD FOR THE DETERMINATION ...

    African Journals Online (AJOL)

    A simple, rapid and sensitive spectrophotometric method has been developed for the determination of iodate (IO3-) in table salt and sea water. The proposed method is based on the reaction of iodate with potassium iodide in an acid medium to liberate iodine. The liberated iodine bleaches the blue color of methylene blue ...

  16. Sorption and speciation of iodine in groundwater system: The roles of organic matter and organic-mineral complexes

    Science.gov (United States)

    Li, Junxia; Zhou, Hailing; Wang, Yanxin; Xie, Xianjun; Qian, Kun

    2017-06-01

    Characterizing the properties of main host of iodine in soil/sediment and the geochemical behaviors of iodine species are critical to understand the mechanisms of iodine mobilization in groundwater systems. Four surface soil and six subsurface sediment samples were collected from the iodine-affected area of Datong basin in northern China to conduct batch experiments and to evaluate the effects of NOM and/or organic-mineral complexes on iodide/iodate geochemical behaviors. The results showed that both iodine contents and kf-iodate values had positive correlations with solid TOC contents, implying the potential host of NOM for iodine in soil/sediment samples. The results of chemical removal of easily extracted NOM indicated that the NOM of surface soils is mainly composed of surface embedded organic matter, while sediment NOM mainly occurs in the form of organic-mineral complexes. After the removal of surface sorbed NOM, the decrease in kf-iodate value of treated surface soils indicates that surface sorbed NOM enhances iodate adsorption onto surface soil. By contrast, kf-iodate value increases in several H2O2-treated sediment samples, which was considered to result from exposed rod-like minerals rich in Fe/Al oxyhydroxide/oxides. After chemical removal of organic-mineral complexes, the lowest kf-iodate value for both treated surface soils and sediments suggests the dominant role of organic-mineral complexes on controlling the iodate geochemical behavior. In comparison with iodate, iodide exhibited lower affinities on all (un)treated soil/sediment samples. The understanding of different geochemical behaviors of iodine species helps to explain the occurrence of high iodine groundwater with iodate and iodide as the main species in shallow (oxidizing conditions) and deep (reducing conditions) groundwater.

  17. Combined DFT and XPS investigation of iodine anions adsorption on the sulfur terminated (001) chalcopyrite surface

    Energy Technology Data Exchange (ETDEWEB)

    Li, Kui, E-mail: likui9606@stu.xjtu.edu.cn [School of Nuclear Science and Technology, Xi’an Jiaotong University, Xi’an 710049 (China); Zhao, Yaolin, E-mail: zhaoyaolin@mail.xjtu.edu.cn [School of Nuclear Science and Technology, Xi’an Jiaotong University, Xi’an 710049 (China); Zhang, Peng, E-mail: zp32@qq.com [Sino Shaanxi Nuclear Industry Group, Xi’an 710100 (China); He, Chaohui, E-mail: hechaohui@mail.xjtu.edu.cn [School of Nuclear Science and Technology, Xi’an Jiaotong University, Xi’an 710049 (China); Deng, Jia, E-mail: djkokocase@stu.xjtu.edu.cn [School of Nuclear Science and Technology, Xi’an Jiaotong University, Xi’an 710049 (China); Ding, Shujiang, E-mail: dingsj@mail.xjtu.edu.cn [Department of Applied Chemistry, School of Science, Xi’an Jiaotong University, Xi’an 710049 (China); Shi, Weiqun, E-mail: shiwq@ihep.ac.cn [Key Laboratory of Nuclear Radiation and Nuclear Energy Technology and Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049 (China)

    2016-12-30

    Highlights: • Metal surface sites of (001)-S surface of chalcopyrite show significant chemical affinity to iodide and iodate. • The energetically favorable active site is copper for iodide adsorption and iron for iodate adsorption, respectively. • Iodate undergoes a dissociative adsorption on the copper site of chalcopyrite surface. - Abstract: The adsorption of iodine anions (iodide and iodate) on the sulfur terminated (001) chalcopyrite surface has been systematically investigated combining first-principles calculations based on density functional theory (DFT) with X-ray photoelectron spectroscopy (XPS) measurements. Based on the total energy calculations and geometric optimization, the thermodynamically preferred site was copper atom for iodide adsorption and iron atom for iodate adsorption, respectively. In the case of Cu site mode, the iodate underwent a dissociative adsorption, where one I−O bond of iodate ion was broken and the dissociative oxygen atom adsorbed on the adjacent sulphur site. Projected density of states (PDOS) analysis further clarified the interaction mechanism between active sites of chalcopyrite surface and adsorbates. In addition, full-range XPS spectra qualitatively revealed the presence of iodine on chalcopyrite surface. High resolution XPS spectra of the I 3d peaks after adsorption verified the chemical environment of iodine. The binding energies of 618.8 eV and 623.5 eV for I 3d{sub 5/2} peaks unveiled that the adsorption of iodide and iodate ions on copper-iron sulfide minerals was the result of formation of low solubility metal iodides precipitate. Also two I 3d peaks with low intensity around 618 eV and 630 eV might be related to the inorganic reduction of iodate to iodide by reducing S{sup 2−} ion of chalcopyrite.

  18. Sorption and speciation of iodine in groundwater system: The roles of organic matter and organic-mineral complexes.

    Science.gov (United States)

    Li, Junxia; Zhou, Hailing; Wang, Yanxin; Xie, Xianjun; Qian, Kun

    2017-06-01

    Characterizing the properties of main host of iodine in soil/sediment and the geochemical behaviors of iodine species are critical to understand the mechanisms of iodine mobilization in groundwater systems. Four surface soil and six subsurface sediment samples were collected from the iodine-affected area of Datong basin in northern China to conduct batch experiments and to evaluate the effects of NOM and/or organic-mineral complexes on iodide/iodate geochemical behaviors. The results showed that both iodine contents and k f -iodate values had positive correlations with solid TOC contents, implying the potential host of NOM for iodine in soil/sediment samples. The results of chemical removal of easily extracted NOM indicated that the NOM of surface soils is mainly composed of surface embedded organic matter, while sediment NOM mainly occurs in the form of organic-mineral complexes. After the removal of surface sorbed NOM, the decrease in k f -iodate value of treated surface soils indicates that surface sorbed NOM enhances iodate adsorption onto surface soil. By contrast, k f -iodate value increases in several H 2 O 2 -treated sediment samples, which was considered to result from exposed rod-like minerals rich in Fe/Al oxyhydroxide/oxides. After chemical removal of organic-mineral complexes, the lowest k f -iodate value for both treated surface soils and sediments suggests the dominant role of organic-mineral complexes on controlling the iodate geochemical behavior. In comparison with iodate, iodide exhibited lower affinities on all (un)treated soil/sediment samples. The understanding of different geochemical behaviors of iodine species helps to explain the occurrence of high iodine groundwater with iodate and iodide as the main species in shallow (oxidizing conditions) and deep (reducing conditions) groundwater. Copyright © 2017 Elsevier B.V. All rights reserved.

  19. Nota sôbre a dosagem iodométrica da vitamina C nos frutos cítricos Iodometric determination of vitamin C in citrus fruit juices

    Directory of Open Access Journals (Sweden)

    Gilberto G. Villela

    1943-12-01

    Full Text Available Ascorbic acid was determined in pure aquous solutions and in citrus fruit juices by iodometric, dichlorophenolindophenol and iodate methods. More constant values were obtained with iodate and Tillmans methods. Iodate is preferable owing to the stability of solution and the simplicity of the method. In the analysis of citrus juices the iodate method proposed by Ballentine is very accurate and suitable for routine work (Table I and II. Recovery experiments recorded in Table III show that the results are reproducible. The averages obtained for some fruits are shown in Table IV. Lemon: 45,4 to 67,3; orange: 28,0 to 60,8; lima: 25,2 to 38,2 and mandarine: 32,0 to 59,3. Values expressed in mg per 100 cc. of juice.

  20. Separation of iodine from mercury containing scrubbing solutions

    Science.gov (United States)

    Burger, Leland L.; Scheele, Randall D.

    1979-01-01

    Radioactive iodines can be recovered from a nitric acid scrub solution containing mercuric nitrate by passing a current through the scrub solution to react the iodine with the mercuric nitrate to form mercuric iodate which precipitates out. The mercuric iodate can then be reacted to recover the radioiodine for further processing into a form suitable for long-term storage and to recover the mercury for recycling.

  1. 127I and 129I Species and Transformation in the Baltic Proper, Kattegat, and Skagerrak Basins

    DEFF Research Database (Denmark)

    Yi, P.; Aldahan, A.; Possnert, G.

    2012-01-01

    , high 127I–/127IO3– and 129I–/129IO3– values suggest effective reduction of iodate with a maximum rate of 8 × 10–7 (127IO3–) and 6 × 10–14 (129IO3–) (g/m3.day). The reduction process of iodate seems to be related to decomposition of organic matter and photochemically induced reactions....

  2. Hydrothermal synthesis, structure, Raman spectroscopy, and self-irradiation studies of 248Cm(IO3)3

    International Nuclear Information System (INIS)

    Sykora, Richard E.; Assefa, Zerihun; Haire, Richard G.; Albrecht-Schmitt, Thomas E.

    2004-01-01

    The study of curium iodate, Cm(IO 3 ) 3 , was undertaken as part of a systematic investigation of the 4f- and 5f-elements' iodates. The reaction of 248 CmCl 3 with aqueous H 5 IO 6 under mild hydrothermal conditions results in the reduction of IO 6 5- to IO 3 - anions, and the subsequent formation of Cm(IO 3 ) 3 single crystals. Crystallographic data are: (193K, MoKα, λ=0.71073A): monoclinic, space group P2 1 /c, a=7.2014(7)A, b=8.5062(9)A, c=13.4622(14)A, β=100.142(2) o , V=811.76(14), Z=4, R(F)=2.11%, Rw(Fo2)=4.43% for 119 parameters with 1917 reflections with I>2σ(I). The structure consists of Cm 3+ cations bound by iodate anions to form [Cm(IO 3 ) 8 ] units, where the local coordination environment around the curium centers can be described as a distorted dodecahedron. There are three crystallographically unique iodate anions within the structure; two iodates bridge between three Cm centers, and one iodate bridges between two Cm centers and has a terminal oxygen atom. The bridging of the curium centers by the iodate anions creates a three-dimensional structure. Three strong Raman bands with comparable intensities were observed at 846, 804, and 760cm -1 and correspond to the I-O symmetric stretching of the three crystallographically distinct iodate ions. The Raman profile suggests a lack of inter-ionic vibrational coupling of the I-O stretching, while intra-ionic coupling provides symmetric and asymmetric components that correspond to each iodate site. Repeated collection of X-ray diffraction data for a crystal of Cm(IO 3 ) 3 over a period of time revealed a gradual expansion of the unit cell from self-irradiation. After 71 days, the new parameters were: a=7.2132(7)A, b=8.5310(8)A, c=13.505(1)A, β=100.021(2) o , V=818.3(2)

  3. Effect of Co-Contaminants Uranium and Nitrate on Iodine Remediation

    Energy Technology Data Exchange (ETDEWEB)

    Szecsody, James E. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Lee, Brady D. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Lawter, Amanda R. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Qafoku, Nikolla [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Resch, Charles T. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Baum, Steven R. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Leavy, Ian I. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Freedman, Vicky L. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

    2017-09-01

    The objective of this study is to evaluate the significance of co-contaminants on the migration and transformation of iodine species in the Hanford subsurface environment. These impacts are relevant because remedies that target individual contaminants like iodine, may not only impact the fate and transport of other contaminants in the subsurface, but also inhibit the effectiveness of a targeted remedy. For example, iodine (as iodate) co-precipitates with calcite, and has been identified as a potential remedy because it immobilizes iodine. Since uranium also co-precipitates with calcite in field sediments, the presence of uranium may also inhibit iodine co-precipitation. Another potentially significant impact from co-existing contaminants is iodine and nitrate. The presence of nitrate has been shown to promote biogeochemical reduction of iodate to iodide, thereby increasing iodine species subsurface mobility (as iodide exhibits less sorption). Hence, this study reports on both laboratory batch and column experiments that investigated a) the change in iodate uptake mass and rate of uptake into precipitating calcite due to the presence of differing amounts of uranium, b) the amount of change of the iodate bio-reduction rate due to the presence of differing nitrate concentrations, and c) whether nitrite can reduce iodate in the presence of microbes and/or minerals acting as catalysts.

  4. Oxidation of iodide and iodine on birnessite (delta-MnO2) in the pH range 4-8.

    Science.gov (United States)

    Allard, Sébastien; von Gunten, Urs; Sahli, Elisabeth; Nicolau, Rudy; Gallard, Hervé

    2009-08-01

    The oxidation of iodide by synthetic birnessite (delta-MnO(2)) was studied in perchlorate media in the pH range 4-8. Iodine (I(2)) was detected as an oxidation product that was subsequently further oxidized to iodate (IO(3)(-)). The third order rate constants, second order on iodide and first order on manganese oxide, determined by extraction of iodine in benzene decreased with increasing pH (6.3-7.5) from 1790 to 3.1M(-2) s(-1). Both iodine and iodate were found to adsorb significantly on birnessite with an adsorption capacity of 12.7 microM/g for iodate at pH 5.7. The rate of iodine oxidation by birnessite decreased with increasing ionic strength, which resulted in a lower rate of iodate formation. The production of iodine in iodide-containing waters in contact with manganese oxides may result in the formation of undesired iodinated organic compounds (taste and odor, toxicity) in natural and technical systems. The probability of the formation of such compounds is highest in the pH range 5-7.5. For pH iodine is quickly oxidized to iodate, a non-toxic and stable sink for iodine. At pH >7.5, iodide is not oxidized to a significant extent.

  5. Iodine speciation in coastal and inland bathing waters and seaweeds extracts using a sequential injection standard addition flow-batch method.

    Science.gov (United States)

    Santos, Inês C; Mesquita, Raquel B R; Bordalo, Adriano A; Rangel, António O S S

    2015-02-01

    The present work describes the development of a sequential injection standard addition method for iodine speciation in bathing waters and seaweeds extracts without prior sample treatment. Iodine speciation was obtained by assessing the iodide and iodate content, the two inorganic forms of iodine in waters. For the determination of iodide, an iodide ion selective electrode (ISE) was used. The indirect determination of iodate was based on the spectrophotometric determination of nitrite (Griess reaction). For the iodate measurement, a mixing chamber was employed (flow batch approach) to explore the inherent efficient mixing, essential for the indirect determination of iodate. The application of the standard addition method enabled detection limits of 0.14 µM for iodide and 0.02 µM for iodate, together with the direct introduction of the target water samples, coastal and inland bathing waters. The results obtained were in agreement with those obtained by ICP-MS and a colorimetric reference procedure. Recovery tests also confirmed the accuracy of the developed method which was effectively applied to bathing waters and seaweed extracts. Copyright © 2014 Elsevier B.V. All rights reserved.

  6. Chlorination of iodide-containing waters in the presence of CuO: Formation of periodate

    KAUST Repository

    Liu, Chao

    2014-11-18

    It has been shown previously that the disproportionation of halogen-containing oxidants (e.g., HOCl, HOBr, and ClO2) is enhanced by a CuO-catalyzed process. In this study, the transformation of iodine during chlorination in the presence of CuO was investigated. There is no significant enhancement of the disproportionation of hypoiodous acid (HOI) in the presence of CuO. The formation rate of iodate (IO3 -) in the CuO-HOCl-I- system significantly increased when compared to homogeneous solutions, which was ascribed to the activation of HOCl by CuO enhancing its reactivity toward HOI. In this reaction system, iodate formation rates increase with increasing CuO (0-0.5 g L-1) and bromide (0-2 μM) doses and with decreasing pH (9.6-6.6). Iodate does not adsorb to the CuO surfaces used in this study. Nevertheless, iodate concentrations decreased after a maximum was reached in the CuO-HOCl-I-(-Br-) systems. Similarly, the iodate concentrations decrease as a function of time in the CuO-HOCl-IO3 - or CuO-HOBr-IO3 - system, and the rates increase with decreasing pH (9.6-6.6) due to the enhanced reactivity of HOCl or HOBr in the presence of CuO. It could be demonstrated that iodate is oxidized to periodate by a CuO-activated hypohalous acid, which is adsorbed on the CuO surface. No periodate could be measured in filtered solutions because it was mainly adsorbed to CuO. The adsorbed periodate was identified by scanning electron microscopy plus energy dispersive spectroscopy and X-ray photoelectron spectroscopy.

  7. Selective Precipitation of Thorium lodate from a Tartaric Acid-Hydrogen Peroxide Medium Application to Rapid Spectrophotometric Determination of Thorium in Silicate Rocks and in Ores

    Science.gov (United States)

    Grimaldi, F.S.

    1957-01-01

    This paper presents a selective iodate separation of thorium from nitric acid medium containing d-tartaric acid and hydrogen peroxide. The catalytic decomposition of hydrogen peroxide is prevented by the use of 8quinolinol. A few micrograms of thorium are separated sufficiently clean from 30 mg. of such oxides as cerium, zirconium, titanium, niobium, tantalum, scandium, or iron with one iodate precipitation to allow an accurate determination of thorium with the thoronmesotartaric acid spectrophotometric method. The method is successful for the determination of 0.001% or more of thorium dioxide in silicate rocks and for 0.01% or more in black sand, monazite, thorite, thorianite, eschynite, euxenite, and zircon.

  8. Iodine levels in Edible Salt Sold in Malawi, Kenya and Zambia ...

    African Journals Online (AJOL)

    This study reveals some weaknesses in the salt iodination programmes in these countries and recommends strict and periodic monitoring of the quality of the salts. Key Words: iodate, salt, Kenya, Malawi, Zambia. TENEURS EN IODE DANS LE SEL COMESTIBLE VENDU AU MALAWI, AU KENYA ET EN ZAMBIE RESUME

  9. Speciation of 129I in sea, lake and rain waters

    DEFF Research Database (Denmark)

    Lehto, Jukka; Räty, Tero; Hou, Xiaolin

    2012-01-01

    Concentrations of the very long-lived fission product 129I and stable iodine (127I) in the Baltic Sea and lake and rain waters from Finland, were measured as well as their occurrence as iodide (I−) and iodate (IO3−). The highest concentrations of both 127I and 129I occurred in sea water, on avera...

  10. Tracing variability in the iodine isotopes and species along surface water transect from the North Sea to the Canary Islands

    DEFF Research Database (Denmark)

    He, Peng; Aldahan, Ala; Hou, Xiaolin

    2016-01-01

    A complete transect of surface water samples from the North Sea to the Canary Islands was collected during a continuous period in 2010. The samples were analyzed for total 129I and 127I isotopes and their iodide and iodate species. The results indicate a large variability in the total 129I and its...

  11. Study in rabbits of portal circulation by a radioisotopic method

    International Nuclear Information System (INIS)

    Maliska, C.

    1980-01-01

    The development of a precocius - and noninvasive method for the detection of portal circulation alterations by means of time interval measurements between the rectal administration of radiotracers and their detection in liver and head is aimed at. The pertecnetate ( 99 sup(m)Tc)- and iodate ( 131 I) absorption by the terminal large intestine was tested in 22 rabbits. The time iinterval between rectal administration of the radiotracer and its appearance in liver and head was determined in 12 rabbits, by external detection with a scintillation camera. The same parameters were studied in 9 animals submitted to the ligature of the portal vein. Iodate and pertecnetate are absorbed by the terminal large intestine, the pertecnetate absorption being significantly smaller than that of iodate. The pertecnetate distribution volume is smaller than that of iodate; the rectum - liver - and rectum - head time intervals is increased in animals with the ligature of portal vein. Application of the method to larger animals will permit the necessary improvements for its utilization as a precocius - noninvasive - and inocuous test in the evaluation of alteration of the human portal circulation. (Author) [pt

  12. Synthesis, characterization and ion exchange properties of ...

    Indian Academy of Sciences (India)

    Abstract. Zirconium(IV) tungstoiodophosphate has been synthesized under a variety of conditions. The most chemically and thermally stable sample is prepared by adding a mixture of aqueous solutions of 0⋅5 mol L–1 sodium tungstate, potassium iodate and 1 mol L–1 orthophosphoric acid to aqueous solution of 0⋅1 mol ...

  13. Water Circulation and Marine Environment in the Antarctic Traced by Speciation of 129I and 127I

    DEFF Research Database (Denmark)

    Xing, Shan; Hou, Xiaolin; Aldahan, Ala

    2017-01-01

    ) and Antarctic Peninsula Coastal Current (APCC). These interactions happen in restricted circulation pathways that may partly relate to glacial melting and icebergs transport. Biological activity during the warm season should be one of the key factors controlling the reduction of iodate in the coastal water...

  14. Iodine Status of School-children (8-10 years) and Associated ...

    African Journals Online (AJOL)

    Almost all (96%) household salt samples were adequately iodated. Frequency of consuming selected iodine-rich foods by the children was low. while consumption of some goitrogen-containing foods was relatively high- It is concluded that inadequate knowledge regarding iodine nutrition, low consumption of iodine-rich ...

  15. Monochloramine determination using NN diethyl-p-phenylene-diamine. Influence of iodide traces

    International Nuclear Information System (INIS)

    Fiquet, J.M.

    1980-09-01

    When determining ''D.P.D.'' free oxidizers, the monochloramine interfers in particular for iodide levels analogous to those likely to be found in sea water. This is not so for iodate. The zero time extrapolation of the change in colour curve is one method that enables the method to be made more selective [fr

  16. 1195-IJBCS-Article-Akpona Simon

    African Journals Online (AJOL)

    DR GATSING

    Organisation. Mondiale de la Santé (OMS), 30% de la population mondiale (1,5 milliard d'individus) étaient exposés à un risque de carence en iode. (Delange, 2001). L'OMS a donc recommandé l'iodation universelle du sel comme stratégie.

  17. Preparation and characterization of activated carbons from rice

    African Journals Online (AJOL)

    270-mesh sieve (BS) instead of a 325 mesh sieve, and standardisation of sodium thiosulphate solution was made using potassium iodate instead of metallic copper. Sample weights were between 0.5 and 1.0 g. The method and procedure for the determination of methylene blue number was followed as given by Mkayula ...

  18. 129I and its species in the East China Sea: level, distribution, sources and tracing water masses exchange and movement

    DEFF Research Database (Denmark)

    Liu, Dan; Hou, Xiaolin; Du, Jinzhou

    2016-01-01

    , and 129I level in seawater declines towards the ECS shelf. In the open sea, 129I and 127I in surface water exists mainly as iodate, while in Yangtze River estuary and some locations, iodide is dominated. The results indicate that the Fukushima nuclear accident has no detectable effects in the ECS until...

  19. Evaporation of iodine-containing off-gas scrubber solution

    Science.gov (United States)

    Partridge, J.A.; Bosuego, G.P.

    1980-07-14

    Mercuric nitrate-nitric acid scrub solutions containing radioiodine may be reduced in volume without excessive loss of volatile iodine. The use of concentrated nitric acid during an evaporation process oxidizes the mercury-iodide complex to a less volatile mercuric iodate precipitate.

  20. NRPB 'pill'

    International Nuclear Information System (INIS)

    Martin, S.; Arnott, D.

    1985-01-01

    The National Radiological Protection Board circulated a leaflet entitled 'Advice for general practitioners in the event of a civil nuclear emergency' in July 1985 to doctors' surgeries in the vicinity of nuclear power stations in England and Wales. The leaflet is reviewed and the scientific background to the 'anti-radiation' potassium iodate pill is explained. (author)

  1. Untitled

    Indian Academy of Sciences (India)

    1951-02-02

    THE OXIDATION OF HYDRO GEN SULPHIDE. BY POTASSIUM IO)ATE. BY A. R. WASUDEVA MURTHY AND B. SANJIVA RAO. (Indian Institute of Science, Bangalore). Received February 2, 1951. DEAN studied the oxidation of Sulphides with potassium iodate and found that the amount of Sulphir oxidised to Sulphiric acid ...

  2. Bulletin of Materials Science | Indian Academy of Sciences

    Indian Academy of Sciences (India)

    Zirconium(IV) tungstoiodophosphate has been synthesized under a variety of conditions. The most chemically and thermally stable sample is prepared by adding a mixture of aqueous solutions of 0.5 mol L-1 sodium tungstate, potassium iodate and 1 mol L-1 orthophosphoric acid to aqueous solution of 0.1 mol L-1 ...

  3. Uptake mechanism for iodine species to black carbon.

    Science.gov (United States)

    Choung, Sungwook; Um, Wooyong; Kim, Minkyung; Kim, Min-Gyu

    2013-09-17

    Natural organic matter (NOM) plays an important role in determining the fate and transport of iodine species such as iodide (I(-)) and iodate (IO3(-)) in groundwater system. Although NOM exists as diverse forms in environments, prior iodine studies have mainly focused on uptake processes of iodide and iodate to humic materials. This study was conducted to determine the iodide and iodate uptake potential for a particulate NOM (i.e., black carbon [BC]). A laboratory-produced BC and commercial humic acid were used for batch experiments to compare their iodine uptake properties. The BC exhibited >100 times greater uptake capability for iodide than iodate at low pH of ~3, while iodide uptake was negligible for the humic acid. The uptake properties of both solids strongly depend on the initial iodine aqueous concentrations. After uptake reaction of iodide to the BC, X-ray absorption fine structure spectroscopy results indicated that the iodide was converted to electrophilic species, and iodine was covalently bound to carbon atom in polycyclic aromatic hydrocarbons present in the BC. The computed distribution coefficients (i.e., Kd values) suggest that the BC materials retard significantly the transport of iodide at low pH in environmental systems containing even a small amount of BC.

  4. Buoyancy-driven convection may switch between reactive states in three-dimensional chemical waves

    Czech Academy of Sciences Publication Activity Database

    Šebestíková, Lenka; Hauser, M. J. B.

    2012-01-01

    Roč. 85, č. 3 (2012), s. 036303 ISSN 1539-3755 R&D Projects: GA ČR GAP105/10/0919 Institutional research plan: CEZ:AV0Z20600510 Keywords : buoyancy-driven convection * chemical waves * iodate-arsenous acid reaction Subject RIV: BK - Fluid Dynamics Impact factor: 2.313, year: 2012

  5. Synthesis and structure of In(IO3)3 and vibrational spectroscopy of M(IO3)3 (M=Al, Ga, In)

    International Nuclear Information System (INIS)

    Ngo, Nhan; Kalachnikova, Katrina; Assefa, Zerihun; Haire, Richard G.; Sykora, Richard E.

    2006-01-01

    The reaction of Al, Ga, or In metals and H 5 IO 6 in aqueous media at 180 o C leads to the formation of Al(IO 3 ) 3 , Ga(IO 3 ) 3, or In(IO 3 ) 3 , respectively. Single-crystal X-ray diffraction experiments have shown In(IO 3 ) 3 contains the Te 4 O 9 -type structure, while both Al(IO 3 ) 3 and Ga(IO 3 ) 3 are known to exhibit the polar Fe(IO 3 ) 3 -type structure. Crystallographic data for In(IO 3 ) 3 , trigonal, space group R3-bar , a=9.7482(4)A, c=14.1374(6)A, V=1163.45(8) Z=6, R(F)=1.38% for 41 parameters with 644 reflections with I>2σ(I). All three iodate structures contain group 13 metal cations in a distorted octahedral coordination environment. M(IO 3 ) 3 (M=Al, Ga) contain a three-dimensional network formed by the bridging of Al 3+ or Ga 3+ cations by iodate anions. With In(IO 3 ) 3 , iodate anions bridge In 3+ cations in two-dimensional layers. Both materials contain distorted octahedral holes in their structures formed by terminal oxygen atoms from the iodate anions. The Raman spectra have been collected for these metal iodates; In(IO 3 ) 3 was found to display a distinctively different vibrational profile than Al(IO 3 ) 3 or Ga(IO 3 ) 3 . Hence, the Raman profile can be used as a rapid diagnostic tool to discern between the different structural motifs

  6. Modelling radioiodine transport across a capillary fringe

    International Nuclear Information System (INIS)

    Mathias, Simon A.; Butler, Adrian P.; Wheater, Howard S.

    2008-01-01

    Due to its long radioactive half-life, iodine-129 is considered to be an important radionuclide in the context of underground radioactive waste disposal safety assessment. Iodine speciates as iodide (I - ) in reducing conditions and iodate (IO 3 - ) in oxidizing conditions. As iodate is more reactive, it is much less mobile than iodide. Consequently, in considering vertically upward transport within a soil profile, iodine will tend to accumulate at the top of the capillary fringe. In this paper, a model of iodine transport across a capillary fringe is developed by coupling equations for variably saturated flow, oxygen dynamics and rate-limited sorption. Model parameters are obtained by consideration of literature values, calibration on soil column data and other supporting laboratory experiments. The results demonstrate the importance of rate kinetics on the migration and bioavailability of radioiodine in the near-surface environment

  7. Modelling radioiodine transport across a capillary fringe.

    Science.gov (United States)

    Mathias, Simon A; Butler, Adrian P; Wheater, Howard S

    2008-04-01

    Due to its long radioactive half-life, iodine-129 is considered to be an important radionuclide in the context of underground radioactive waste disposal safety assessment. Iodine speciates as iodide (I-) in reducing conditions and iodate (IO3-) in oxidizing conditions. As iodate is more reactive, it is much less mobile than iodide. Consequently, in considering vertically upward transport within a soil profile, iodine will tend to accumulate at the top of the capillary fringe. In this paper, a model of iodine transport across a capillary fringe is developed by coupling equations for variably saturated flow, oxygen dynamics and rate-limited sorption. Model parameters are obtained by consideration of literature values, calibration on soil column data and other supporting laboratory experiments. The results demonstrate the importance of rate kinetics on the migration and bioavailability of radioiodine in the near-surface environment.

  8. Iodine isotopes species fingerprinting environmental conditions in surface water along the northeastern Atlantic Ocean

    DEFF Research Database (Denmark)

    He, Peng; Hou, Xiaolin; Aldahan, Ala

    2013-01-01

    Concentrations and species of iodine isotopes (127I and 129I) provide vital information about iodine geochemistry, environmental conditions and water masses exchange in oceans. Despite extensive investigations of anthropogenic 129I in the Arctic Ocean and the Nordic Seas, concentrations of the is...... 129I in ocean environments and impact on climate at the ocean boundary layer.......Concentrations and species of iodine isotopes (127I and 129I) provide vital information about iodine geochemistry, environmental conditions and water masses exchange in oceans. Despite extensive investigations of anthropogenic 129I in the Arctic Ocean and the Nordic Seas, concentrations...... of the isotope in the Atlantic Ocean are, however, still unknown. We here present first data on 129I and 127I, and their species (iodide and iodate) in surface water transect along the northeastern Atlantic between 30° and 50°N. The results show iodate as the predominant species in the analyzed marine waters...

  9. Speciation Analysis and Environmental Tracer Studies of 129I

    DEFF Research Database (Denmark)

    Zhang, Luyuan

    , Japan were investigated. Iodate for both 129I and 127I is the predominant form for the seawater in the central Arctic and Greenland coast, whereas iodide is the major specie of 129I and 127I in Danish coast. A distinct distribution pattern of iodine species was observed in Fukushima offshore seawater......, such as the Greenland Sea, and the western Atlantic Ocean, as well as to the atmosphere and the Arctic ecosystem. Aerosol samples collected at two locations (Risø, Denmark, a coastal site, and Tsukuba Japan, about 170 km southwest of the Fukushima Dai-ichi nuclear power plant) during spring 2011 (shortly after...... in real samples demonstrate that the developed method is reliable for accurate determination of 129I and 127I species in aerosol samples. Distributions of chemical species (iodide and iodate) of 129I and 127I in the seawater from the central Arctic, Greenland coast, Danish coast and offshore Fukushima...

  10. Acute and Subacute Oral Toxicity of Periodate in Rats

    Science.gov (United States)

    2014-11-17

    Transient increases in gastrointestinal pH and degeneration of parietal cells, hemolytic effects including hemoglobinuria and hemosiderin deposits in...doses of iodate being reduced to the less toxic iodide when in contact with food in the gastrointestinal tract. The toxicity of periodate to the...prostration and dyspnea. Excitability, convulsions and paresis of the hind legs frequently preceded death. Transient increases in gastrointestinal pH

  11. Transitions Between Convective Patterns in Chemical Fronts

    OpenAIRE

    Wu, Y.; Vasquez, D. A.; Edwards, Boyd F.; Wilder, J. W.

    1995-01-01

    We present a theory for the transition from nonaxisymmetric to axisymmetric convection in iodate-arsenous acid reaction fronts propagating in a vertical slab. The transition takes place away from the onset of convection, where a convectionless flat front becomes unstable to a nonaxisymmetric convective front. The transition is studied by numerically solving a reaction-diffusion equation coupled with nonlinear hydrodynamics in a two-dimensional slab.

  12. Quantitative determination of some water-soluble B vitamins by kinetic analytical method based on the perturbation of an oscillatory reaction

    OpenAIRE

    Maksimović,Jelena P.; Kolar-Anić,Ljiljana Z.; Anić,Slobodan R.; Ribić,Dragana D.; Pejić,Nataša D.

    2011-01-01

    A novel procedure for kinetic determination of some water-soluble vitamins of the B-group (thiamine (B1), riboflavin (B2), niacin (B3) and pyridoxine (B6)) by the concentration perturbations of the Bray-Liebhafsky (BL) oscillatory chemical system involving the catalytic decomposition of hydrogen peroxide in the presence of both hydrogen and iodate ions is proposed and validated. The method uses a Pt electrode for potentiometric monitoring of the concentration perturbations of the BL matrix in...

  13. Optimized and Validated Spectrophotometric Methods for the Determination of Enalapril Maleate in Commercial Dosage Forms

    OpenAIRE

    Rahman, Nafisur; Haque, Sk Manirul

    2008-01-01

    Four simple, rapid and sensitive spectrophotometric methods have been proposed for the determination of enalapril maleate in pharmaceutical formulations. The first method is based on the reaction of carboxylic acid group of enalapril maleate with a mixture of potassium iodate (KIO3) and iodide (KI) to form yellow colored product in aqueous medium at 25 ± 1°C .The reaction is followed spectrophotometrically by measuring the absorbance at 352 nm. The second, third and fourth methods are based o...

  14. Predicted formation constants using the unified theory of metal ion complexation

    International Nuclear Information System (INIS)

    Brown, P.L.; Wanner, H.

    1987-01-01

    Formation constants are listed for standard conditions, i.e., 298.15K (25 0 C), 10 5 Pa, and zero ionic strength for a number of species containing selected elements (Am, Cs, Np, Pa, Pb, Pd, Pu, Ra, Sn, Sr, Tc, Th, U) and ligands (hydroxide, fluoride, chloride, bromide, iodide, iodate, sulphate, ammonia, nitrate, hydrogen phosphate, dihydrogen phosphate, carbonate, bicarbonate, oxalate, formate, thiocyanate, acetate, benzoate, catecholate, ethylenediamine, glycinate, glycollate and phenolate) that have been considered important for nuclear technology. 16 refs

  15. Laboratory report on iodine (129I and 127I) speciation, transformation and mobility in Handford groundwater, suspended particles and sediments

    Energy Technology Data Exchange (ETDEWEB)

    Santschi, P. H. [Texas A & M Univ., College Station, TX (United States); Xu, C. [Texas A & M Univ., College Station, TX (United States); Zhang, S. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Ho, Y. [Texas A & M Univ., College Station, TX (United States); Li, H. [Texas A & M Univ., College Station, TX (United States); Schwehr, K. [Texas A & M Univ., College Station, TX (United States); Kaplan, D. I. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2012-09-01

    The Hanford Site in eastern Washington produced plutonium for several decades and in the process generated billions of gallons of radioactive waste. Included in this complex mixture of waste was 50 Ci of iodine-129 (129I). Iodine-129’s high abundance, due to its high fission yield, and extreme toxicity result in iodine-129 becoming a key risk driver at many Department of Energy (DOE) sites. The mobility of radioiodine in arid environments, such as the Hanford Site, depends largely on its chemical speciation and is also greatly affected by many other environmental factors, especially natural sediment organic matter (SOM). Groundwater radioiodine speciation has not been measured in arid regions with major plumes or large disposed 129I inventories, including the Hanford Site, Idaho National Laboratory, and Nevada Test Site. In this study, stable iodine-127 and radioiodine-129 speciation, pH, and dissolved organic carbon (DOC) of groundwater samples collected from seven wells located in the 200-West Area of the Hanford site were investigated. The most striking finding was that iodate (IO3-) was the most abundant species. Unexpectedly, iodide (I-), which was likely the form of iodine in the source materials and the expected dominant groundwater species based on thermodynamic considerations, only accounted for 1-2% of the total iodine concentration. It is likely that the relatively high pH and the low abundance of sedimentary organic matter (SOM) that is present at the site slowed down or even inhibited the reduction of iodate, as SOM abiotically reduce iodate into iodide. Moreover, a study on the kinetics of iodide and iodate uptake and aqueous speciation transformation by three representative subsurface Hanford sediments was performed over a period of about one month. This study was carried out by using iodide-125 or iodate-125 at the ambient iodine-127concentration found at the site. Iodate Kd values

  16. The potential role of kelp forests on iodine speciation in coastal seawater.

    Directory of Open Access Journals (Sweden)

    Jennifer Gonzales

    Full Text Available Kelps have a major role in marine and atmospheric iodine cycling in the coastal zone of temperate regions, with potential wide-ranging impacts on ozone destruction in the coastal marine boundary layer. However, little is known about the impact of kelp forests on iodine speciation in coastal sea water. To address this, we examined iodide and iodate concentrations in seawater in and around a giant kelp forest near San Diego, CA, USA, and a nearby site that was not influenced by kelp biology. Our data shows that while both iodide and iodate concentrations remained unchanged during the year at the nearby site, these concentrations changed significantly in and around the kelp forest, and were strongly related to changes in kelp canopy biomass. In particular, iodide reached its highest concentration and iodate reached its lowest concentration during the summer when the kelp canopies were near their maximum, while the opposite pattern was observed during the winter and spring when the kelp canopies were near their minimum. Further, comparisons of these changes with corresponding changes in seawater temperature and wind speed indicated that these relationships were relatively small compared to those with changes in kelp biomass. Together, our data show a strong relationship between kelp biomass and iodine metabolism.

  17. Marine geochemistry of iodine

    International Nuclear Information System (INIS)

    Kennedy, H.; Elderfield, H.

    1985-01-01

    Iodine has long been classified as a biophilic element with analyses showing that iodine is strongly enriched, relative to seawater concentrations in both plankton and particulate matter and that the concentration of iodine found in surface sediments is still further enriched relative to that found in the sedimenting particulate matter. The extent of enrichment of iodine relative to carbon in deep sea surface sediments has been shown to depend on the carbon accumulation rate. Iodine decomposition rates have been calculated and are shown to vary with the sedimentation rate in the same manner as has been shown for organic carbon. Vertical profiles of total dissolved iodine, iodate and iodide in interstitial waters of sediments from the north east Atlantic are characterised by three zones of reaction as identified by changes in the concentration of iodate and iodide. These reaction zones represent (i) iodide production (ii) iodide oxidation and (iii) iodate reduction. Pore water and solid phase iodine profiles from cores containing turbidite units have shown that iodine, released to pore waters as iodide during the oxidation of the organic matter, has been scavenged after diffusing upwards into a less reducing region of the sediment. (author)

  18. The potential role of kelp forests on iodine speciation in coastal seawater.

    Science.gov (United States)

    Gonzales, Jennifer; Tymon, Teresa; Küpper, Frithjof C; Edwards, Matthew S; Carrano, Carl J

    2017-01-01

    Kelps have a major role in marine and atmospheric iodine cycling in the coastal zone of temperate regions, with potential wide-ranging impacts on ozone destruction in the coastal marine boundary layer. However, little is known about the impact of kelp forests on iodine speciation in coastal sea water. To address this, we examined iodide and iodate concentrations in seawater in and around a giant kelp forest near San Diego, CA, USA, and a nearby site that was not influenced by kelp biology. Our data shows that while both iodide and iodate concentrations remained unchanged during the year at the nearby site, these concentrations changed significantly in and around the kelp forest, and were strongly related to changes in kelp canopy biomass. In particular, iodide reached its highest concentration and iodate reached its lowest concentration during the summer when the kelp canopies were near their maximum, while the opposite pattern was observed during the winter and spring when the kelp canopies were near their minimum. Further, comparisons of these changes with corresponding changes in seawater temperature and wind speed indicated that these relationships were relatively small compared to those with changes in kelp biomass. Together, our data show a strong relationship between kelp biomass and iodine metabolism.

  19. Simultaneous quantification of iodine and high valent metals via ICP-MS under acidic conditions in complex matrices.

    Science.gov (United States)

    Brix, Kristina; Hein, Christina; Sander, Jonas Michael; Kautenburger, Ralf

    2017-05-15

    The determination of iodine as a main fission product (especially the isotopes I-129 and I-131) of stored HLW in a disposal beside its distribution as a natural ingredient of many different products like milk, food and seawater is a matter of particular interest. The simultaneous ICP-MS determination of iodine as iodide together with other elements (especially higher valent metal ions) relevant for HLW is analytically very problematic. A reliable ICP-MS quantification of iodide must be performed at neutral or alkaline conditions in contrast to the analysis of metal ions which are determined in acidic pH ranges. Herein, we present a method to solve this problem by changing the iodine speciation resulting in an ICP-MS determination of iodide as iodate. The oxidation from iodide to iodate with sodium hypochlorite at room temperature is a fast and convenient method with flexible reaction time, from one hour up to three days, thus eliminating the disadvantages of quantifying iodine species via ICP-MS. In the analysed concentration range of iodine (0.1-100µgL -1 ) we obtain likely quantitative recovery rates for iodine between 91% and 102% as well as relatively low RSD values (0.3-4.0%). As an additional result, it is possible to measure different other element species in parallel together with the generated iodate, even high valent metals (europium and uranium beside caesium) at recovery rates in the same order of magnitude (93-104%). In addition, the oxidation process operates above pH 7 thus offering a wide pH range for sample preparation. Even analytes in complex matrices, like 5M saline (NaCl) solution or artificial cement pore water (ACW) can be quantified with this robust sample preparation method. Copyright © 2017 Elsevier B.V. All rights reserved.

  20. Geochemical Cycling of Iodine Species in Soils

    Energy Technology Data Exchange (ETDEWEB)

    Hu, Q; Moran, J E; Blackwood, V

    2007-08-23

    Iodine is an important element in studies of environmental protection and human health, global-scale hydrologic processes and nuclear nonproliferation. Biogeochemical cycling of iodine in soils is complex, because iodine occurs in multiple oxidation states and as inorganic and organic species that may be hydrophilic, atmophilic, and biophilic. In this study, we applied new analytical techniques to study the content and speciation of stable iodine in representative surface soils, and sorption and transport behavior of iodine species (iodide, iodate, and 4-iodoaniline) in sediments collected at numerous nuclear facilities in the United States, where anthropogenic {sup 129}I from prior nuclear fuel processing activities poses an environmental risk. The surface soil samples were chosen for their geographic locations (e.g., near the ocean or nuclear facilities) and for their differing physico-chemical characteristics (organic matter, texture, etc). Extracted solutions were analyzed by IC and ICP-MS methods to determine iodine concentrations and to examine iodine speciation (iodide, iodate, and organic iodine). In natural soils, iodine is mostly (nearly 90% of total iodine) present as organic species, while inorganic iodine becomes important (up to 50%) only in sediments with low organic matter. Results from laboratory column studies, aimed at examining transport of different iodine species, showed much greater retardation of 4-iodoaniline than iodide or iodate. Careful attention must be given to potential interconversion among species when interpreting the biogeochemical behavior of iodine in the environment. In addition to speciation, input concentration and residence time effects will influence the biogeochemical cycling of anthropogenic 129I deposited on surface soils.

  1. Leading safety performance indicators for resilience assessment of radiopharmaceuticals production process

    International Nuclear Information System (INIS)

    Grecco, Claudio H.S.; Santos, Isaac J.A.L.; Carvalho, Paulo V.R.

    2011-01-01

    Radiopharmaceuticals are radiation-emitting substances used in medicine for radiotherapy and imaging diagnosis. A Research Institute, located in Rio de Janeiro, produces three radiopharmaceuticals: the sodium iodate is used in the diagnosis of thyroid dysfunctions, the meta-iodo-benzyl guanidine is used in the diagnosis of cardiac diseases, and the fluorodeoxyglucose is used in diagnosis in cardiology, oncology, neurology and neuro psychiatry. This paper presents a leading safety performance indicators framework to assess the resilience of radiopharmaceuticals production processes. The organizations that use resilience indicators will be able to pro actively evaluate and manage safety. (author)

  2. Salts of the iodine oxyacids in the impregnation of adsorbent charcoal for trapping radioactive methyliodide

    International Nuclear Information System (INIS)

    1980-01-01

    A method of removing methyliodide 131 gas from the effluent of a reactor, comprises passing the effluent gas through a charcoal sorbent formed by first contacting charcoal with a liquid containing a hypoiodite obtained when an aqueous mixture of a first component comprising a salt of an iodine oxyacid selected from periodate, iodate and hypoiodite and a second component selected from iodine and/or an iodide salt is adjusted to a pH of about 10 by the addition of an inorganic base, and then contacting the resulting impregnated charcoal with a tertiary amine. (author)

  3. Method to remove methyl iodide131 gas

    International Nuclear Information System (INIS)

    Deitz, V.R.; Blachly, C.H.

    1977-01-01

    A two-stage impregnation process for charcoal is presented which is to be used for radioactive iodine or methyl iodide removal from the waste gas of a nuclear reactor. In the first stage, the coal is treated at pH 10 with an aqueous mixture of a salt of iodic acid (hypoiodite, iodate, or periodate) with iodine or iodide. In the second stage, impregnation with a tertiary amine occurs. The concentrations are chosen so that the charcoal will take up between 0.5 and 4% by weight of iodine. (UWI) [de

  4. Pylorogastric intussusception in a Chihuahua puppy. A case report.

    Science.gov (United States)

    Lideo, L; Mutinelli, F; Milan, R

    2010-12-01

    A three-month-old Chihuahua dog was presented with acute abdominal pain, vomiting and cardiovascular shock. Abdominal ultrasound (US) and iodated contrast gastrogram revealed suspected pylorogastric intussusception. Because of the poor prognosis the dog was euthanatized. Diagnosis of pylorogastric intussusception was confirmed at necropsy. Parasitological, virological, serological and histological examinations were also performed. This report documents the sixth case of pylorogastric (i.e. duodenogastric, gastrogastric) intussusception in the veterinary medical literature and it is the first report on a puppy dog in which US and radiographic diagnosis were confirmed post mortem.

  5. Leading safety performance indicators for resilience assessment of radiopharmaceuticals production process

    Energy Technology Data Exchange (ETDEWEB)

    Grecco, Claudio H.S.; Santos, Isaac J.A.L.; Carvalho, Paulo V.R., E-mail: grecco@ien.gov.b, E-mail: luquetti@ien.gov.b, E-mail: paulov@ien.gov.b [Instituto de Engenharia Nuclear (IEN/CNEN-RJ), Rio de Janeiro, RJ (Brazil). Div. de Instrumentacao e Confiabilidade Humana; Vidal, Mario C.R., E-mail: mvidal@ergonomia.ufrj.b [Coordenacao dos Programas de Pos-Graduacao de Engenharia (PEP/COPPE/UFRJ), Rio de Janeiro, RJ (Brazil). Programa de Engenharia de Producao. Grupo de Ergonomia e Novas Tecnologias (GENTE)

    2011-07-01

    Radiopharmaceuticals are radiation-emitting substances used in medicine for radiotherapy and imaging diagnosis. A Research Institute, located in Rio de Janeiro, produces three radiopharmaceuticals: the sodium iodate is used in the diagnosis of thyroid dysfunctions, the meta-iodo-benzyl guanidine is used in the diagnosis of cardiac diseases, and the fluorodeoxyglucose is used in diagnosis in cardiology, oncology, neurology and neuro psychiatry. This paper presents a leading safety performance indicators framework to assess the resilience of radiopharmaceuticals production processes. The organizations that use resilience indicators will be able to pro actively evaluate and manage safety. (author)

  6. Chemical speciation analysis and environmental behaviour of 127I and 12

    International Nuclear Information System (INIS)

    Hansen, Violeta

    2011-10-01

    Chemical speciation analysis of 129 I and 127 I as iodide, iodate and total inorganic iodine in seawater samples from the Baltic Proper, Skagerrak and Kattegat has been carried out. The important findings of this study are that the reduction of iodate and oxidation of iodide in Skagerrak and Kattegat may be a slow process while along the Baltic Sea surface water reduction of iodate is a relatively fast process. Although suboxic or anoxic condition are encountered in some of the Baltic Sea deep basins, the concentration of 129 IO 3 - increases with water depth indicating that the reduction of iodate in the oxygen deficient bottom water of the Baltic Sea is a slow process. Iodine chemical speciation analysis (as iodide, iodate and total iodine including inorganic and organic iodine species) in lake water samples collected from Denmark and southern Sweden has been carried out. Destruction of organic iodine was performed by alkaline oxidation using NaOH - NaClO at 100 deg. C and anion exchange chromatography was used for separation of iodide and iodate. Iodine-129 concentrations in the lakes ranged from 1.3 - 12.8 x10 9 at/L and show elevated concentrations in lakes located in southwest Jutland (Denmark), near the North Sea. Except the Skaersoe Lake, were the organic iodine - 127 accounts for 50% of the total iodine, iodide (both 129 I and 127 I) is the predominant species form in surface water of the studied lakes. An investigation was conducted in order to quantify the total aquatic iodine ( 129 I and 127 I as inorganic and organic iodine) from fresh water and seawater samples by adsorption onto activated charcoal and DEAE 32 cellulose followed by alkaline digestion or combustion. The results show that iodide from freshwater samples can easily be adsorbed onto activated charcoal. The sorption was not affected by the pH. The absorption capacity of iodate is low and reduces quickly when its concentration increases. Compared with activated charcoal, DEAE 32 cellulose

  7. Stannous ion quantitation in sup(99m)Tc-radiopharmaceutical kits

    International Nuclear Information System (INIS)

    Chervu, L.R.; Vallabhajosyula, B.; Mani, J.; Chun, S.B.; Blaufox, M.D.

    1982-01-01

    A simple and inexpensive method for the estimation of stannous ion, Sn(II), in radiopharmaceutical kits is described. The method used is a potentiometric titration of Sn(II) in 1 N HCl medium, using potassium iodate as the oxidizing agent in an atmosphere of nitrogen. The apparatus includes a pH meter, a platinum electrode, and a simple titration cell. Several commonly used radiopharmaceutical kits were analyzed for their Sn(II) content using this method. These studies indicate that the procedure can be used, as a routine quantitative test for the Sn(II) content of various sup(99m)Tc-labeled radiopharmaceuticals. (orig.)

  8. Determination of small amounts of nitric acid in the presence of large amounts of uranium (VI) and extraction of nitric acid into TBP solutions highly loaded with uranyl nitrate

    International Nuclear Information System (INIS)

    Kolarik, Z.; Schuler, R.

    1982-10-01

    A new method for the determination of small amounts of nitric acid in the presence of large amounts of uranium(VI) was elaborated. The method is based on the precipitation of uranium(VI) as iodate and subsequent alkalimetric titration of the acid in the supernatant. The extraction of nitric acid and uranium(VI) with 30% TBP in dodecane was studied at high loading of the organic phase with uranyl nitrate and at 25, 40 and 60 0 C. The results are compared with available published data on the extraction of nitric acid under similar conditions. (orig.) [de

  9. Determination of inorganic radioiodine in 131I- Rose Bengal and 131I- bromosulphthalein

    International Nuclear Information System (INIS)

    Toledo e Souza, I.T. de; Pereira, N.P.S. de; Silva, C.P.G. da.

    1985-01-01

    A rapid miniaturized chromatographic system was developed for fast determination of the proportion of inorganic radioactive iodide from radiopharmaceuticals 131 I-Rose Bengal and 131 I-Bromosulphthalein. Using 33% W/V aqueous solution of ammonium sulphate pH 7,5 as a solvent Rf values for radiopharmaceuticals, iodide, iodate to Rf 0,0 0,5 0,9 respectively. The chromatographic quality control procedures are easy to use, rapid and can be incorporated in a routine quality control program. (Author) [pt

  10. Relation between shape of liquid-gas interface and evolution of buoyantly unstable three-dimensional chemical fronts

    Czech Academy of Sciences Publication Activity Database

    Šebestíková, Lenka

    2013-01-01

    Roč. 88, č. 3 (2013), , 033023-1-033023-7 ISSN 1539-3755 R&D Projects: GA ČR GAP105/10/0919 Institutional research plan: CEZ:AV0Z20600510 Institutional support: RVO:67985874 Keywords : iodate-arsenous acid reaction * arsenous acid * concave meniscus * convex meniscus * buoyancy driven convection * chemical waves Subject RIV: BK - Fluid Dynamics; CI - Industrial Chemistry, Chemical Engineering (UCHP-M); CC - Organic Chemistry (UOCHB-X) Impact factor: 2.326, year: 2013

  11. Policy on stable iodine prophylaxis following nuclear reactor accidents (1989)

    International Nuclear Information System (INIS)

    1989-09-01

    This policy considers the alleviation of possible hazards that may arise from any radioiodines inhaled from a plume of fission products emanating from a nuclear reactor accident. Such a nuclear reactor may be land or ship-based. In any accident that releases radioiodines to the environment, one countermeasure that may need to be considered to reduce the effect of inhalation of radioiodines by persons downwind of the point of release is to provide those persons with tablets containing stable iodine. Both potassium iodide (KI) and potassium iodate (KIO 3 ) are recommended as effective prophylactics tablets for this purpose in Australia. Action levels, doses and contraindicatories are briefly outlined

  12. Saccharomyces cerevisiae: the effect of different forms and concentrations of iodine on uptake and yeast growth.

    Science.gov (United States)

    Osterc, Andrej; Fujs, Stefan; Raspor, Peter; Stibilj, Vekoslava

    2009-02-01

    The essentiality of iodine for humans, especially in the early stages of life, is well recognized. The chemical forms of iodine in food supplements, infant formulae and iodated salt are either iodide (KI) or iodate (KIO(3)). Because there are no or rare data about iodine uptake by yeasts, we investigated the influence of different sources of iodine, as KI, KIO(3) and periodate (KIO(4)), on its uptake in and growth of the model yeast Saccharomyces cerevisiae. KIO(3) inhibited the growth of the yeast the most and already at a 400 microM initial concentration in the growth medium; the OD was reduced by 23% in comparison with the control, where no KIO(3) was added. The uptake of different iodine sources by the yeast S. cerevisiae was minimal, in total yeast S. cerevisiae does not have the ability to transform KI into volatile species. We investigated the specificity of iodine uptake added as KIO(3) in the presence of Na(2)SeO(4) or ZnCl(2) or K(2)CrO(4) in the growth medium, and it was found that chromate had the most influence on reduction of KIO(3) uptake.

  13. Iodine deficiency persists in the Zanzibar Islands of Tanzania.

    Science.gov (United States)

    Assey, V D; Greiner, T; Mzee, R K; Abuu, H; Mgoba, C; Kimboka, S; Peterson, S

    2006-12-01

    Iodine is an essential micronutrient for normal human growth and development. It is estimated that more than 1.6 billion people live in iodine-deficient environments, yet there are still some countries and areas where the prevalence of iodine-deficiency disorders is unknown. To establish the prevalence of iodine-deficiency disorders in the Zanzibar Islands, a community assumed to have ready access to iodine-rich seafoods. In a cross-sectional study, 11,967 schoolchildren were palpated for goiter prevalence, a subsample was evaluated for urinary iodine concentration, and the availability of iodated salt was assessed at the household and retail levels. The mean total goiter prevalence was 21.3% for Unguja and 32.0% for Pemba. The overall median urinary iodine concentration was 127.5 microg/L. For Unguja the median was 185.7 microg/L, a higher value than the median of 53.4 microg/L for Pemba (p Zanzibar Islands belies the common assumption that an island population with access to seafood is not at risk for iodine-deficiency disorders. We urge health planners to implement mandatory salt iodation and education efforts to alleviate the situation.

  14. Incorporation of iodine into calcium phosphates with apatitic structure

    International Nuclear Information System (INIS)

    Coulon, Antoine

    2014-01-01

    In order to avoid the release of 129 I (long-lived intermediate-level waste) in the environment, we describe a novel material incorporating iodine under the form of iodate in a calcium phosphate based hydroxyapatite. This material is prepared by two synthetic processes: a wet precipitation route followed by a spark plasma sintering and a cementitious route. A high iodine content (with a maximum incorporation rate of 10 wt.%) is reached for both processes, by incorporation of the iodate in the apatitic structure. A monolith with relative density of 88.6% was obtained after shaping of the precipitated powders by spark plasma sintering. This material reveals satisfactory leaching properties, with an initial leaching rate in pure water at 50 C of 10 -2 g.m -2 .j -1 , and a residual leaching rate at 50 C of 10 -5 g.m -2 .j -1 in underground water of potential geological repositories. All in all, this material is a potential candidate for the conditioning of radioactive iodine. (author) [fr

  15. New method for preparation of polyoxometalate-capped gold nanoparticles, and their assembly on an indium-doped tin oxide electrode

    International Nuclear Information System (INIS)

    Cheng, Y.; Zheng, J.; Wang, Z.; Liu, L.; Wu, Y.; Yang, J.

    2011-01-01

    Functionalized gold nanoparticles capped with polyoxometalates were prepared by a simple photoreduction technique where phosphododecamolybdates serve as reducing reagents, photocatalysts, and as stabilizers. TEM images of the resulting gold nanoparticles show the particles to have a relative narrow size distribution. Monolayer and multilayer structures of the negatively charged capped gold nanoparticles were deposited on a poly(vinyl pyridine)-derivatized indium-doped tin oxide (ITO) electrode via the layer-by-layer technique. The surface plasmon resonance band of the gold nanoparticles displays a blue shift on the surface of the ITO electrode. This is due to the substrate-induced charge redistribution in the gold nanoparticles and a change in the electromagnetic coupling between the assembled nanoparticles. The modified electrode exhibits the characteristic electrochemical behavior of surface-confined phosphododecamolybdate and excellent electrocatalytic activity. The catalysis of the modified electrode towards the model compound iodate was systematically studied. The heterogeneous catalytic rate constant for the electrochemical reduction of iodate was determined by chronoamperometry to be ca. 1. 34 x 10 5 mol -1 .L.s -1 . The amperometric method gave a linear range from 2. 5 x 10 -6 to 1. 5 x 10 -3 M and a detection limit of 1. 0 x 10 -6 M. We believe that the functionalized gold nanoparticles prepared by this photoreduction technique are advantageous in terms of fabrication of sensitive and stable redox electrodes. (author)

  16. Modern and ancient geochemical constraints on Proterozoic atmosphere-ocean redox evolution

    Science.gov (United States)

    Hardisty, D. S.; Horner, T. J.; Wankel, S. D.; Lu, Z.; Lyons, T.; Nielsen, S.

    2017-12-01

    A detailed understanding of the spatiotemporal oxygenation of Earth's atmosphere-ocean system through the Precambrian has important implications for the environments capable of sustaining early eukaryotic life and the evolving oxidant budget of subducted sediments. Proxy records suggest an anoxic Fe-rich deep ocean through much of the Precambrian and atmospheric and surface-ocean oxygenation that started in earnest at the Paleoproterozoic Great Oxidation Event (GOE). The marine photic zone represented the initial site of oxygen production and accumulation via cyanobacteria, yet our understanding of surface-ocean oxygen contents and the extent and timing of oxygen propagation and exchange between the atmosphere and deeper ocean are limited. Here, we present an updated perspective of the constraints on atmospheric, surface-ocean, and deep-ocean oxygen contents starting at the GOE. Our research uses the iodine content of Proterozoic carbonates as a tracer of dissolved iodate in the shallow ocean, a redox-sensitive species quantitatively reduced in modern oxygen minimum zones. We supplement our understanding of the ancient record with novel experiments examining the rates of iodate production from oxygenated marine environments based on seawater incubations. Combining new data from iodine with published shallow marine (Ce anomaly, N isotopes) and atmospheric redox proxies, we provide an integrated view of the vertical redox structure of the atmosphere and ocean across the Proterozoic.

  17. Immobilized organoruthenium(II) complexes onto polyethyleneimine-wrapped carbon nanotubes/in situ formed gold nanoparticles as a novel electrochemical sensing platform

    Energy Technology Data Exchange (ETDEWEB)

    Azadbakht, Azadeh, E-mail: Azadbakht.a@gmail.com; Abbasi, Amir Reza; Derikvand, Zohreh; Amraei, Shiba

    2015-03-01

    The polyethyleneimine (PEI) wrapped multi-walled carbon nanotubes functionalized with a carboxylic acid group (CNTs–COOH) gold nanoparticle (AuNP)-modified gold (Au) electrode has been utilized as a platform to immobilize organoruthenium(II) complexes (ORC). The surface structure and composition of the sensor were characterized by scanning electron microscopy (SEM). Electrocatalytic reduction of iodate and nitrite on the surface of modified electrode was investigated with cyclic voltammetry, electrochemical impedance spectroscopy (EIS) and hydrodynamic voltammetry methods. The cyclic voltammetric results indicated the ability of AuNPs/PEI/CNT–COOH/ORC modified Au electrode to catalyze the reduction of this compound. AuNPs/PEI/CNTs–COOH nanocomposite combined the advantages of PEI-well dispersed CNTs–COOH and in situ formed AuNPs. - Highlights: • We prepared composite containing polyethyleneimine (PEI), CNTs and AuNPs. • AuNPs were in situ formed on the surface of CNTs–PEI. • When the AuNPs were in situ formed the stability would be improved. • Nanocomposite combined the advantages of PEI–CNTs and in situ formed AuNPs. • Modified nanocomposite Au electrode catalyzes the reduction of iodate and nitrite.

  18. Synthesis, Crystal Structure, and Topology-Symmetry Analysis of a New Modification of NaIn[IO3]4

    Science.gov (United States)

    Belokoneva, E. L.; Karamysheva, A. S.; Dimitrova, O. V.; Volkov, A. S.

    2018-01-01

    Crystals of new iodate NaIn[IO3]4 were prepared by the hydrothermal synthesis. The unit cell parameters are a = 7.2672(2) Å, b = 15.2572(6) Å, c = 15.0208(6) Å, β = 101.517(3)°, sp. gr. P21/ c. The formula was determined during the structure determination and refinement of a twinned crystal based on a set of reflections from the atomic planes of the major individual. The refinement with anisotropic displacement parameters was performed for both twin components to the final R factor of 0.050. The In and Na atoms are in octahedral coordination formed by oxygen atoms. The oxygen octahedra are arranged into columns by sharing edges, and the columns are connected by isolated umbrella-like [IO3]- groups to form layers. The new structure is most similar to the isoformular iodate NaIn[IO3]4, which crystallizes in the same sp. gr. P21/ c and is structurally similar, but has a twice smaller unit cell and is characterized by another direction of the monoclinic axis. The structural similarity and difference between the two phases were studied by topologysymmetry analysis. The formation of these phases is related to different combinations of identical one-dimensional infinite chains of octahedra.

  19. Circulating Reactive Oxidant Causes Apoptosis of Retinal Pigment Epithelium and Cone Photoreceptors in the Mouse Central Retina

    Directory of Open Access Journals (Sweden)

    Wei Wang

    2011-01-01

    Full Text Available Reactive oxidants damage the retinal pigment epithelium (RPE, which is required for viability of overlying photoreceptors. Smoking which leads to chronic accumulation of reactive oxidants in the circulation is linked to age-related macular degeneration (AMD where RPE death is seen along with photoreceptor loss in the central macular region of the retina. It is unclear why this damage is concentrated in the central retina. We asked whether circulating oxidant might specifically target the central retina. Mice were administered the classic reactive oxidant iodate through tail vein injection, and visual acuity was followed by optokinetic response. Histology and apoptosis was examined by H&E and immunostaining. Iodate indeed selectively damaged the central retina, and this damage was highlighted by early apoptosis of RPE in the central retina followed by apoptosis of photoreceptors adjacent to the region of RPE loss–-cones were lost preferentially. The pattern and extent of this damage was independent of exposure to light. We then conclude that circulating oxidant is sufficient to selectively damage the central retina highlighted by sequential apoptosis of RPE and photoreceptors, with cones being the most sensitivity to this RPE loss.

  20. Iodine Speciation in Marine Aerosol of the Atlantic Ocean (AMT21)

    Science.gov (United States)

    Yodle, Chan; von Glasow, Roland; Baker, Alex

    2014-05-01

    Iodine chemistry in marine aerosol plays important roles in the marine boundary layer such as ozone destruction and new aerosol particle formation. In both cases, the speciation of iodine is an important factor in determining the role of iodine in these processes. Iodine has a complex chemistry in the gas and aerosol phases and to date the interactions and roles of individual iodine species are not well understood. This study will present results of a research cruise from the Atlantic Ocean, AMT21, which travelled from Avonmouth in the UK to Punta Arenas, Chile during September to November 2011. Aerosol samples were collected for 24 hours onto pre-cleaned glass fibre filters with a flow rate of ~1 m3 min-1, using a total suspended particulate sampler. Collected aerosol samples were extracted into ultra-pure water using mechanical shaking at room temperature. Iodine speciation in these extracts was measured using ion-chromatography coupled to Inductively Coupled Plasma-Spectrometry (IC-ICP-MS). Soluble organic iodine (SOI) was then determined by differences between the sum of inorganic iodine (iodide and iodate) and total soluble iodine determined by ICP-MS. Chemical analysis of major ions was also analysed by ion chromatography. Back trajectories were used to categorise air masses of aerosol, according to their origins and transport pathways. Results show considerable differences in the iodine speciation of fine and coarse aerosol particles. These differences of iodine proportions in both aerosol modes agree well with previous studies in the Atlantic. Iodate was dominant species in coarse mode aerosol, its concentration ranged from 4.4 to 58.4 pmol m-3 (median proportion 80%), while SOI and iodide were found in lower concentrations. SOI concentrations ranged from 0.5 to 6.4 pmol m-3 (median proportion 12%) and iodide concentrations ranged from 0.6 to 4.6 pmol m-3 (median proportion 9%) respectively. For fine mode aerosol, lower iodate concentrations were observed

  1. CAUSE OF A MULTI-SPECIES RADIOIODINE PLUME THAT IS INCREASING IN CONCENTRATION

    Energy Technology Data Exchange (ETDEWEB)

    Kaplan, D.

    2010-09-30

    Field and laboratory studies were carried out to understand the cause for steady increases in {sup 129}I concentrations emanating from radiological seepage basins located on the Savannah River Site. The basins were closed in 1988 by adding limestone and blast furnace slag and then capping with a RCRA low permeability engineered cover. Groundwater {sup 129}I concentrations in a well near the seepage basin in 1993 were 200 pCi L{sup -1} and are presently between 400 and 1000 pCi L{sup -1}. Iodine speciation in the plume was not uniform. Near the source, the iodine was comprised of 86% iodide, 2% iodate, and 12% organo-iodine (total activity = 178 pCi L{sup -1}). Whereas, groundwater iodine speciation 365 m down stream (25 m up stream from a wetland) was 0% iodide, 93% iodate, and 7% organo iodine. Batch desorption studies demonstrated that high concentrations of {sup 129}I could be incrementally desorbed from an archived seepage basin sediment sample by raising the pH. Batch sorption studies showed that iodate, IO{sub 3}{sup -}, sorbed more strongly than iodide, I{sup -}, to a subsurface clayey sediment, but equally well as iodide to a subsurface sandy sediment and a wetland sediment. Placing an organic-rich wetland sediment, but not nearby mineral sediments, under reducing (or microaerobic) conditions resulted in a large decrease in iodide K{sub d} values (from 73 to 10 mL g{sup -1}) and iodate K{sub d} values (from 80 to 7 mL g{sup -1}). Between pH and reduction-oxidation potential, it appears that pH seems to have a stronger influence on iodide and iodate sorption to mineral sediment. This may not be true for sediments containing higher concentrations of organic matter, such as the 7.6% organic matter sediment used in this study. First order calculations based on desorption studies with seepage basin sediments indicate that the modest increase of 0.7 pH units detected in the study site groundwater over the last 17 years since closure of the seepage basin may be

  2. Chemical speciation analysis and environmental behaviour of 127I and 129I

    Energy Technology Data Exchange (ETDEWEB)

    Hansen, Violeta

    2011-10-15

    Chemical speciation analysis of 129I and 127I as iodide, iodate and total inorganic iodine in seawater samples from the Baltic Proper, Skagerrak and Kattegat has been carried out. The important findings of this study are that the reduction of iodate and oxidation of iodide in Skagerrak and Kattegat may be a slow process while along the Baltic Sea surface water reduction of iodate is a relatively fast process. Although suboxic or anoxic condition are encountered in some of the Baltic Sea deep basins, the concentration of 129IO{sub 3}- increases with water depth indicating that the reduction of iodate in the oxygen deficient bottom water of the Baltic Sea is a slow process. Iodine chemical speciation analysis (as iodide, iodate and total iodine including inorganic and organic iodine species) in lake water samples collected from Denmark and southern Sweden has been carried out. Destruction of organic iodine was performed by alkaline oxidation using NaOH - NaClO at 100 deg. C and anion exchange chromatography was used for separation of iodide and iodate. Iodine-129 concentrations in the lakes ranged from 1.3 - 12.8 x109 at/L and show elevated concentrations in lakes located in southwest Jutland (Denmark), near the North Sea. Except the Skaersoe Lake, were the organic iodine - 127 accounts for 50% of the total iodine, iodide (both 129I and 127I) is the predominant species form in surface water of the studied lakes. An investigation was conducted in order to quantify the total aquatic iodine (129I and 127I as inorganic and organic iodine) from fresh water and seawater samples by adsorption onto activated charcoal and DEAE 32 cellulose followed by alkaline digestion or combustion. The results show that iodide from freshwater samples can easily be adsorbed onto activated charcoal. The sorption was not affected by the pH. The absorption capacity of iodate is low and reduces quickly when its concentration increases. Compared with activated charcoal, DEAE 32 cellulose showed

  3. Photodecomposition of iodinated contrast media and subsequent formation of toxic iodinated moieties during final disinfection with chlorinated oxidants.

    Science.gov (United States)

    Allard, Sébastien; Criquet, Justine; Prunier, Anaïs; Falantin, Cécilia; Le Person, Annaïg; Yat-Man Tang, Janet; Croué, Jean-Philippe

    2016-10-15

    Large amount of iodinated contrast media (ICM) are found in natural waters (up to μg.L(-)(1) levels) due to their worldwide use in medical imaging and their poor removal by conventional wastewater treatment. Synthetic water samples containing different ICM and natural organic matter (NOM) extracts were subjected to UV254 irradiation followed by the addition of chlorine (HOCl) or chloramine (NH2Cl) to simulate final disinfection. In this study, two new quantum yields were determined for diatrizoic acid (0.071 mol.Einstein(-1)) and iotalamic acid (0.038 mol.Einstein(-1)) while values for iopromide (IOP) (0.039 mol.Einstein(-1)), iopamidol (0.034 mol.Einstein(-1)) and iohexol (0.041 mol.Einstein(-1)) were consistent with published data. The photodegradation of IOP led to an increasing release of iodide with increasing UV doses. Iodide is oxidized to hypoiodous acid (HOI) either by HOCl or NH2Cl. In presence of NOM, the addition of oxidant increased the formation of iodinated disinfection by-products (I-DBPs). On one hand, when the concentration of HOCl was increased, the formation of I-DBPs decreased since HOI was converted to iodate. On the other hand, when NH2Cl was used the formation of I-DBPs was constant for all concentration since HOI reacted only with NOM to form I-DBPs. Increasing the NOM concentration has two effects, it decreased the photodegradation of IOP by screening effect but it increased the number of reactive sites available for reaction with HOI. For experiments carried out with HOCl, increasing the NOM concentration led to a lower formation of I-DBPs since less IOP are photodegraded and iodate are formed. For NH2Cl the lower photodegradation of IOP is compensated by the higher amount of NOM reactive sites, therefore, I-DBPs concentrations were constant for all NOM concentrations. 7 different NOM extracts were tested and almost no differences in IOP degradation and I-DBPs formation was observed. Similar behaviour was observed for the 5 ICM

  4. Mechanistic, kinetic, and processing aspects of tungsten chemical mechanical polishing

    Science.gov (United States)

    Stein, David

    This dissertation presents an investigation into tungsten chemical mechanical polishing (CMP). CMP is the industrially predominant unit operation that removes excess tungsten after non-selective chemical vapor deposition (CVD) during sub-micron integrated circuit (IC) manufacture. This work explores the CMP process from process engineering and fundamental mechanistic perspectives. The process engineering study optimized an existing CMP process to address issues of polish pad and wafer carrier life. Polish rates, post-CMP metrology of patterned wafers, electrical test data, and synergy with a thermal endpoint technique were used to determine the optimal process. The oxidation rate of tungsten during CMP is significantly lower than the removal rate under identical conditions. Tungsten polished without inhibition during cathodic potentiostatic control. Hertzian indenter model calculations preclude colloids of the size used in tungsten CMP slurries from indenting the tungsten surface. AFM surface topography maps and TEM images of post-CMP tungsten do not show evidence of plow marks or intergranular fracture. Polish rate is dependent on potassium iodate concentration; process temperature is not. The colloid species significantly affects the polish rate and process temperature. Process temperature is not a predictor of polish rate. A process energy balance indicates that the process temperature is predominantly due to shaft work, and that any heat of reaction evolved during the CMP process is negligible. Friction and adhesion between alumina and tungsten were studied using modified AFM techniques. Friction was constant with potassium iodate concentration, but varied with applied pressure. This corroborates the results from the energy balance. Adhesion between the alumina and the tungsten was proportional to the potassium iodate concentration. A heuristic mechanism, which captures the relationship between polish rate, pressure, velocity, and slurry chemistry, is presented

  5. Novel molecular-level evidence of iodine binding to natural organic matter from Fourier transform ion cyclotron resonance mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Xu, Chen, E-mail: xuchen66@tamu.edu [Laboratory for Environmental and Oceanographic Research, Department of Marine Sciences, Texas A and M University, Building 3029, Galveston, TX 77551 (United States); Chen, Hongmei [Department of Chemistry and Biochemistry, Old Dominion University, Norfolk, VA 23529 (United States); Sugiyama, Yuko [Department of Chemistry and Biochemistry, Old Dominion University, Norfolk, VA 23529 (United States); University of Hyogo, 1-1-12, Shinzaike-honcho, Himeji, Hyogo 670-0092 (Japan); Zhang, Saijin; Li, Hsiu-Ping; Ho, Yi-Fang; Chuang, Chia-ying; Schwehr, Kathleen A. [Laboratory for Environmental and Oceanographic Research, Department of Marine Sciences, Texas A and M University, Building 3029, Galveston, TX 77551 (United States); Kaplan, Daniel I. [Savannah River National Laboratory, Aiken, SC 29808 (United States); Yeager, Chris [Los Alamos National Laboratory, Los Alamos, NM 87545 (United States); Roberts, Kimberly A. [Savannah River National Laboratory, Aiken, SC 29808 (United States); Hatcher, Patrick G. [Department of Chemistry and Biochemistry, Old Dominion University, Norfolk, VA 23529 (United States); Santschi, Peter H. [Laboratory for Environmental and Oceanographic Research, Department of Marine Sciences, Texas A and M University, Building 3029, Galveston, TX 77551 (United States)

    2013-04-01

    Major fractions of radioiodine ({sup 129}I) are associated with natural organic matter (NOM) in the groundwater and surface soils of the Savannah River Site (SRS). Electrospray ionization coupled to Fourier transform ion cyclotron resonance mass spectrometry (ESI-FTICR-MS) was applied to elucidate the interactions between inorganic iodine species (iodide and iodate) and a fulvic acid (FA) extracted from a SRS surface soil. Iodate is likely reduced to reactive iodine species by the lignin- and tannin-like compounds or the carboxylic-rich alicyclic molecules (CRAM), during which condensed aromatics and lignin-like compounds were generated. Iodide is catalytically oxidized into reactive iodine species by peroxides, while FA is oxidized by peroxides into more aliphatic and less aromatic compounds. Only 9% of the total identified organo-iodine compounds derived from molecules originally present in the FA, whereas most were iodine binding to newly-produced compounds. The resulting iodinated molecules were distributed in three regions in the van Krevelen diagrams, denoting unsaturated hydrocarbons, lignin and protein. Moreover, characteristics of these organo-iodine compounds, such as their relatively low O/C ratios (< 0.2 or < 0.4) and yet some degree of un-saturation close to that of lignin, have multiple important environmental implications concerning possibly less sterically-hindered aromatic ring system for iodine to get access to and a lower hydrophilicity of the molecules thus to retard their migration in the natural aquatic systems. Lastly, ∼ 69% of the identified organo-iodine species contains nitrogen, which is presumably present as -NH{sub 2} or -HNCOR groups and a ring-activating functionality to favor the electrophilic substitution. The ESI-FTICR-MS technique provides novel evidence to better understand the reactivity and scavenging properties of NOM towards radioiodine and possible influence of NOM on {sup 129}I migration. Highlights: ► IO{sub 3}{sup

  6. Separation of KI and KIO3 using 1,4 dioxane

    International Nuclear Information System (INIS)

    Hull, D.R.; Owens, C.W.

    1975-01-01

    A simple and quick procedure was elaborated for the separation of KI and KIO 3 and subsequent scintillation counting. KI-KIO 3 mixture was dissolved in one ml ammoniacal water (pH 8) and 6.5 ml carefully purified 1,4-dioxane was added. The mixture was thoroughly shaken, allowed to stand for several minutes, then centrifuged 3-5 minutes. The supernatant solution (containg KI) was decanted and the KIO 3 precipitate was redissolved by adding one ml ammoniacal water. Again 1.4-dioxane was added. The supernate is added to the first decanted solution. The combined supernates permits determination of the iodide-radioactivity by liquid scintillation counting. The iodate radioactivity may be similarly determined by dissolving the residual KIO 3 in ammoniacal water. (F.Gy.)

  7. Heat capacity data for selected cesium- and iodine-containing electrolytes in water at elevated temperatures

    Energy Technology Data Exchange (ETDEWEB)

    Saluja, P.P.S.; LeBlanc, J.C.

    1985-09-01

    The results of heat capacity measurements are presented for cesium halides and cesium iodate in water at 0.6 MPa and in the temperature range 25 to 100/sup 0/C. Partial molar heat capacity functions, partial molar heat capacity were evaluated by applying Pitzer's ion-interaction model for the extrapolation of calculated apparent molal heat capacity data, phi/sub c/, to infinite dilution. The partial molar heat capacity values in water depend strongly on the cesium salt and the temperature. For all salts, the partial molar heat capacity functions show maxima in the 75 to 93/sup 0/C range. These data can be used to determine various thermodynamic properties of aqueous cesium and iodine systems at elevated temperatures. 27 refs., 7 figs., 11 tabs.

  8. saltPAD: A New Analytical Tool for Monitoring Salt Iodization in Low Resource Settings

    Directory of Open Access Journals (Sweden)

    Nicholas M. Myers

    2016-03-01

    Full Text Available We created a paper test card that measures a common iodizing agent, iodate, in salt. To test the analytical metrics, usability, and robustness of the paper test card when it is used in low resource settings, the South African Medical Research Council and GroundWork performed independ‐ ent validation studies of the device. The accuracy and precision metrics from both studies were comparable. In the SAMRC study, more than 90% of the test results (n=1704 were correctly classified as corresponding to adequately or inadequately iodized salt. The cards are suitable for market and household surveys to determine whether salt is adequately iodized. Further development of the cards will improve their utility for monitoring salt iodization during production.

  9. Continuous analysis of radioiodine isotopes in the primary coolant of NPP Paks, Hungary

    International Nuclear Information System (INIS)

    Erdoes, E.; Soos, J.; Vincze, A.; Zsille, O.; Gujgiczer, A.; Solymosi, J.; Pinter, T.

    1998-01-01

    The radioiodine analyser has been installed at the Paks-3 reactor unit. The analyser is based on an efficient and simple method of radioiodine separation: the iodine compound is converted to elementary iodine quantitatively by oxidation with potassium iodate in acid medium. Owing to its volatility, iodine is evaporated quantitatively from the primary coolant (desorption) using air flow. The air is bubbled through a solution of a reducer, and iodine is absorbed in a form which is ready for measurement. A simple NaI(Tl) detector is used for the measurement of gamma spectra. The system is controlled and data are processed by a computer. The analyser displays activity concentration data of the five iodine isotopes periodically every 15 minutes. (M.D.)

  10. Gas chromatography-mass spectrometric identification of iodine species arising from photo-chemical vapor generation

    Energy Technology Data Exchange (ETDEWEB)

    Grinberg, Patricia; Mester, Zoltan [Institute for National Measurements Standards, National Research Council Canada, Ottawa, Ontario, K1A 0R6 (Canada); D' Ulivo, Alessandro [Institute for Chemical and Physical Processes, National Research Council, Via G. Moruzzi 1, Pisa, 56124 (Italy); Sturgeon, Ralph E. [Institute for National Measurements Standards, National Research Council Canada, Ottawa, Ontario, K1A 0R6 (Canada)], E-mail: ralph.sturgeon@nrc.ca

    2009-07-15

    Ultraviolet irradiation of aqueous solutions of iodide/iodate ion containing low molecular weight organic acids generates volatile iodine species that are amenable to detection by atomic spectrometry. In the presence of formic, acetic or propionic acids, photo-chemical generation results in the formation of HI, methyl- and ethyl-iodide respectively, the latter two products being directly identified by gas chromatography-mass spectrometry. Deuterium and {sup 13}C-labeled reagents were employed to elucidate the provenance of the alkyl group. Use of {sup 13}CH{sub 3}-COOH produced {sup 13}CH{sub 3}-I; deuterated acetic acid (D{sub 3}C-COOD) resulted in the formation of CD{sub 3}-I. These observations indicate direct transfer of the alkyl group from the carboxylic acid to iodide, consistent with the suggestion that the mechanism of synthesis involves radical induced reactions.

  11. Gas chromatography-mass spectrometric identification of iodine species arising from photo-chemical vapor generation

    Science.gov (United States)

    Grinberg, Patricia; Mester, Zoltan; D'Ulivo, Alessandro; Sturgeon, Ralph E.

    2009-07-01

    Ultraviolet irradiation of aqueous solutions of iodide/iodate ion containing low molecular weight organic acids generates volatile iodine species that are amenable to detection by atomic spectrometry. In the presence of formic, acetic or propionic acids, photo-chemical generation results in the formation of HI, methyl- and ethyl-iodide respectively, the latter two products being directly identified by gas chromatography-mass spectrometry. Deuterium and 13C-labeled reagents were employed to elucidate the provenance of the alkyl group. Use of 13CH 3-COOH produced 13CH 3-I; deuterated acetic acid (D 3C-COOD) resulted in the formation of CD 3-I. These observations indicate direct transfer of the alkyl group from the carboxylic acid to iodide, consistent with the suggestion that the mechanism of synthesis involves radical induced reactions.

  12. On-line separation of iodine species in reactor water using mixer-settlers

    International Nuclear Information System (INIS)

    Malmbeck, R.; Skarnemark, G.

    1995-01-01

    A method for separation of iodine species from water has been developed. It is based on liquid-liquid extraction and separation is achieved in four extraction steps. A system based on this method for continuous separation of iodine species using mixer-settlers has been developed. It consists of four mixer-settler batteries with 4,4,6 and 6 mixer-settler stages each. As organic phase an aliphatic kerosene is used and the separation is improved if the organic solvent has been pretreated with iodine carrier, stripped and washed. With an aqueous feed flowrate of 10 ml/min and mixer-settler battery phase flowratios of approximately 0.1 except for the elementary iodine strip battery with a phase flowratio of 1, the system separation performance is 92% for methyl iodide, 97% for iodate and elementary iodine and 99% for iodide. (orig.)

  13. Eichrom's ABEC trademark resins: Alkaline radioactive waste treatment, radiopharmaceutical, and potential hydrometallurgical applications

    International Nuclear Information System (INIS)

    Bond, A.H.; Gula, M.J.; Chang, F.; Rogers, R.D.

    1997-01-01

    Eichrom's ABEC trademark resins selectivity extract certain anions from high ionic strength acidic, neutral, or strongly alkaline media, and solute stripping can be accomplished by eluting with water. ABEC resins are stable to pH extreme and radiolysis and operate in high ionic strength and/or alkaline solutions where anion-exchange is often ineffective. Potential applications of the ABEC materials include heavy metal and ReO 4 - separations in hydrometallurgy and purification of perrhenate iodide, and iodate in radiopharmaceutical production. Separation of 99m TcO 4 - from its 99 MoO 4 2- parent and stripping with water or physiological saline solution have been demonstrated for radiopharmaceutical applications. Removal of 99 TcO 4 - and 129 I - from alkaline tank wastes has also been successfully demonstrated. The authors will discuss the scale-up studies, process-scale testing, and market development of this new extraction material

  14. Application of strong phosphoric acid to radiochemistry

    International Nuclear Information System (INIS)

    Terada, Kikuo

    1977-01-01

    Not only inorganic and organic compounds but also natural substrances, such as accumulations in soil, are completely decomposed and distilled by heating with strong phosphoric acid for 30 to 50 minutes. As applications of strong phosphoric acid to radiochemistry, determination of uranium and boron by use of solubilization effect of this substance, titration of uranyl ion by use of sulfuric iron (II) contained in this substance, application to tracer experiment, and determination of radioactive ruthenium in environmental samples are reviewed. Strong phosphoric acid is also applied to activation analysis, for example, determination of N in pyrographite with iodate potassium-strong phosphoric acid method, separation of Os and Ru with sulfuric cerium (IV) - strong phosphoric acid method or potassium dechromate-strong phosphoric acid method, analysis of Se, As and Sb rocks and accumulations with ammonium bromide, sodium chloride and sodium bromide-strong phosphoric acid method. (Kanao, N.)

  15. A review of the biological and geochemical behaviour of technetium in the marine environment

    International Nuclear Information System (INIS)

    Beasley, T.M.; Lorz, H.V.

    1986-01-01

    Present understanding of the behavior of Tc in the marine environment is summarised. The prevalent valence state of Tc in oxygenated seawater is +7, arguing that pertechnetate ion, TcO - 4 , represents the most likely form of this radioelement in seawater. Laboratory experiments using radio-labeled pertechnetate ion have shown that binding of this anion to different classes of marine sediments is slight. Concentration factors for the majority of marine organisms studied to date are small; notable exceptions are seen in certain species of brown algae, polychaetes and macrocrustaceans. Uptake and loss kinetics are generally rapid with the majority of the Tc being associated with shell, exoskeleton and gut. There are, as yet, no data supporting the contention that stable element analogs such as iodate can be used to predict the long-term behavior of 99 Tc (as pertechnetate) in the marine environment. (author)

  16. The impact of disulfide bond dynamics in wheat gluten protein on the development of fermented pastry crumb.

    Science.gov (United States)

    Ooms, Nand; Jansens, Koen J A; Pareyt, Bram; Reyniers, Stijn; Brijs, Kristof; Delcour, Jan A

    2018-03-01

    Gluten proteins functionality during pastry production was examined by including redox agents in the ingredient bill. Addition of reducing and oxidizing agents respectively increased and decreased dough height during fermentation. The presence of large gas bubbles in the samples with oxidizing agents may have caused a 'stacking'-effect and a more effective dough lift. During baking, the level of extractable proteins decreased to comparable values for all samples, except when potassium iodate (KIO 3 ) was used in the recipe. As a result of its use, a lower level of gliadin was incorporated into the gluten polymer and dough layers tended to 'slide' apart during baking, thereby causing collapse. Most likely, KIO 3 caused glutenin oxidation within each individual dough layer to such extent during the dough stage that insufficient thiol groups were available for forming dough layer interconnections during baking, after margarine melting. Furthermore, addition of redox agents impacted the product's crumb structure. Copyright © 2017 Elsevier Ltd. All rights reserved.

  17. Action of acoustical oscillations and hydrodynamic factors on the chemical activity of iodne in solution

    International Nuclear Information System (INIS)

    Nikolaev, L.A.; Fadeev, G.N.

    1984-01-01

    Investigation results on the effect of acoustic oscillations within the frequency range of 1-500 Hz on aqueous iodine solutions and dark blue iodide-starch complex have been presented. Experiments were carried out within the range of action of acoustical and hydrodynamic oscillations without visual formation of bubbles. Form of kinetic dependences corresponds to the first order reaction in respect to iodine. Sharp increase of solution electric conductivity and noticeable increase of medium acidity were observed after the action of oscillations. It has been shown that low-frequency oscillations strengthen iodine hydrolysis and lead to iodate atom formation. Effect of oscillations with 25-30 Hz upon the iodide-starch complex results in the complex destruction, i. e. iodide atom chains removal out of clathrate starch cavities. Formation of iodide-starch complexes is promoted under the action of 250 Hz frequency, as such oscillations lead to the change of starch structure, but do not effect upon iodide

  18. The heads and tails of buoyant autocatalytic balls

    Science.gov (United States)

    Rogers, Michael C.; Morris, Stephen W.

    2012-09-01

    Buoyancy produced by autocatalytic reaction fronts can produce fluid flows that advect the front position, giving rise to interesting feedback between chemical and hydrodynamic effects. In this paper, we numerically investigate the evolution of autocatalytic iodate-arsenous acid reaction fronts initialized in spherical configurations. Deformation of these "autocatalytic balls" is driven by buoyancy produced by the reaction. In our simulations, we have found that depending on the initial ball radius, the reaction front will develop in one of three different ways. In an intermediate range of ball size, the flow can evolve much like an autocatalytic plume: the ball develops a reacting head and tail that is akin to the head and conduit of an autocatalytic plume. In the limit of large autocatalytic balls, however, growth of a reacting tail is suppressed and the resemblance to plumes disappears. Conversely, very small balls of product solution fail to initiate sustained fronts and eventually disappear.

  19. Chemical, mass spectrometric, spectrochemical, nuclear, and radiochemical analysis of nuclear-grade plutonium nitrate solutions

    International Nuclear Information System (INIS)

    Anon.

    1981-01-01

    These analytical procedures are designed to show whether a given material meets the purchaser's specifications as to plutonium content, effective fissile content, and impurity content. The following procedures are described in detail: plutonium by controlled-potential coulometry; plutonium by amperometric titration with iron(II); free acid by titration in an oxalate solution; free acid by iodate precipitation-potentiometric titration method; uranium by Arsenazo I spectrophotometric method; thorium by thorin spectrophotometric method; iron by 1,10-phenanthroline spectrophotometric method; chloride by thiocyanate spectrophotometric method; fluoride by distillation-spectrophotometric method; sulfate by barium sulfate turbidimetric method; isotopic composition by mass spectrometry; americium-241 by extraction and gamma counting; americium-241 by gamma counting; gamma-emitting fission products, uranium, and thorium by gamma-ray spectroscopy; rare earths by copper spark spectrochemical method; tungsten, niobium (columbium), and tantalum by spectrochemical method; simple preparation by spectrographic analysis for general impurities

  20. Validation of simultaneous volumetric and spectrophotometric methods for the determination of captopril in pharmaceutical formulations.

    Science.gov (United States)

    Rahman, Nafisur; Singh, Manisha; Hoda, Nasrul

    2005-01-01

    Simple, sensitive and economical simultaneous volumetric and spectrophotometric methods for the determination of captopril have been developed. The methods were based on the reaction of captopril with potassium iodate in HCl medium. Amaranth was used as indicator to detect the end-point of the titration in aqueous layer. The iodine formed during the titration was extracted into CCl4 and subsequently determined spectrophotometrically at 510 nm. The Beer's law was obeyed in the concentration range of 120-520 microg ml-1. Rigorous statistical analyses were performed for the validation of the proposed methods. The proposed methods were successfully applied to the determination of captopril in dosage forms. Comparison of the means of the proposed procedures with those of reference methods using point and interval hypothesis tests showed no statistically significant difference.

  1. A nanosilver-based spectrophotometry method for sensitive determination of tartrazine in food samples.

    Science.gov (United States)

    Sahraei, R; Farmany, A; Mortazavi, S S

    2013-06-01

    A new method is reported for sensitive determination of tartrazine in the food samples. The method is based on the catalytic effect of silver nanoparticle (AgNPs) on the oxidation reaction of tartrazine by potassium iodate in the acetate buffer medium. The reaction is followed spectrophotometrically by measuring the change in absorbance (ΔA) at 420 nm using a fixed time method (70 s). The reaction variables were optimised in order to achieve the highest sensitivity. The thirty six criterion detection limit was 0.3 ng/mL, and the relative standard deviation for ten replicate measurements of 30 ng/mL of tartrazine was 0.98% (n=10). The method was successfully applied to the determination of tartrazine in lemon, and papaya-flavoured gelatin, candy, and in fruit syrup. Copyright © 2012 Elsevier Ltd. All rights reserved.

  2. Standard test methods for chemical, mass spectrometric, spectrochemical, nuclear, and radiochemical analysis of nuclear-grade plutonium nitrate solutions

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2010-01-01

    1.1 These test methods cover procedures for the chemical, mass spectrometric, spectrochemical, nuclear, and radiochemical analysis of nuclear-grade plutonium nitrate solutions to determine compliance with specifications. 1.2 The analytical procedures appear in the following order: Sections Plutonium by Controlled-Potential Coulometry Plutonium by Amperometric Titration with Iron(II) Plutonium by Diode Array Spectrophotometry Free Acid by Titration in an Oxalate Solution 8 to 15 Free Acid by Iodate Precipitation-Potentiometric Titration Test Method 16 to 22 Uranium by Arsenazo I Spectrophotometric Test Method 23 to 33 Thorium by Thorin Spectrophotometric Test Method 34 to 42 Iron by 1,10-Phenanthroline Spectrophotometric Test Method 43 to 50 Impurities by ICP-AES Chloride by Thiocyanate Spectrophotometric Test Method 51 to 58 Fluoride by Distillation-Spectrophotometric Test Method 59 to 66 Sulfate by Barium Sulfate Turbidimetric Test Method 67 to 74 Isotopic Composition by Mass Spectrom...

  3. Simultaneous detection of iodine and iodide on boron doped diamond electrodes.

    Science.gov (United States)

    Fierro, Stéphane; Comninellis, Christos; Einaga, Yasuaki

    2013-01-15

    Individual and simultaneous electrochemical detection of iodide and iodine has been performed via cyclic voltammetry on boron doped diamond (BDD) electrodes in a 1M NaClO(4) (pH 8) solution, representative of typical environmental water conditions. It is feasible to compute accurate calibration curve for both compounds using cyclic voltammetry measurements by determining the peak current intensities as a function of the concentration. A lower detection limit of about 20 μM was obtained for iodide and 10 μM for iodine. Based on the comparison between the peak current intensities reported during the oxidation of KI, it is probable that iodide (I(-)) is first oxidized in a single step to yield iodine (I(2)). The latter is further oxidized to obtain IO(3)(-). This technique, however, did not allow for a reasonably accurate detection of iodate (IO(3)(-)) on a BDD electrode. Copyright © 2012 Elsevier B.V. All rights reserved.

  4. Determination of iodine and iodine compounds in marine samples by ICPMS and HPLC-ICPMS

    DEFF Research Database (Denmark)

    Hansen, Maiken Sødergreen; Lewandowski, Daniel Jacob; Rasmussen, Rie Romme

    2014-01-01

    By now it is a well-known fact that iodine is an essential trace element for the growth and development of the human body. Because of iodine deficiency, some countries have added iodate to salt in order to increase the iodine intake. However, some people prefer iodine from more natural sources like...... seaweed and fish, which contain elevated levels of iodine (fish typically 1-10 mg/kg and seaweed up to 8000 mg/kg). These marine food items may contain different iodine species, which may have different bioavailability and toxicity, and hence there is an increased interest in developing analytical methods...... for determining the different iodine species. For determining the total iodine concentration in marine samples five different extraction methods were compared. The most efficient and precise method was then used for determining the total concentration of iodine in seaweed and fish samples using inductively...

  5. Speciation of the bio-available iodine and bromine forms in edible seaweed by high performance liquid chromatography hyphenated with inductively coupled plasma-mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Romaris-Hortas, Vanessa; Bermejo-Barrera, Pilar [Department of Analytical Chemistry, Nutrition and Bromatology, Faculty of Chemistry, University of Santiago de Compostela, Avenida das Ciencias, s/n. 15782 - Santiago de Compostela (Spain); Moreda-Pineiro, Jorge [Department of Analytical Chemistry, Faculty of Sciences, University of A Coruna, Campus da Zapateira, s/n. 15071, A Coruna (Spain); Moreda-Pineiro, Antonio, E-mail: antonio.moreda@usc.es [Department of Analytical Chemistry, Nutrition and Bromatology, Faculty of Chemistry, University of Santiago de Compostela, Avenida das Ciencias, s/n. 15782 - Santiago de Compostela (Spain)

    2012-10-01

    Highlights: Black-Right-Pointing-Pointer Bioavailable iodine and bromine speciation in edible seaweed were developed. Black-Right-Pointing-Pointer In vitro dialyzability was used to assess the bioavailable fractions. Black-Right-Pointing-Pointer AEC hyphenated with inductively coupled plasma-mass spectrometry was used. Black-Right-Pointing-Pointer Iodide, MIT, DIT, bromide and bromate were found in dialyzates from edible seaweed. Black-Right-Pointing-Pointer Positive correlation between bioavailability and protein contents was found. - Abstract: A bioavailability study based on an in vitro dialyzability approach has been applied to assess the bio-available fractions of iodine and bromine species from edible seaweed. Iodide, iodate, 3-iodo-tyrosine (MIT), 3,5-diiodo-tyrosine (DIT), bromide and bromate were separated by anion exchange chromatography under a gradient elution mode (175 mM ammonium nitrate plus 15% (v/v) methanol, pH 3.8, as a mobile phase, and flow rates within the 0.5-1.5 mL min{sup -1} range). Inductively coupled plasma-mass spectrometry (ICP-MS) was used as a selective detector for iodine ({sup 127}I) and bromine ({sup 79}Br). Low dialyzability ratios (within the 2.0-18% range) were found for iodine species; whereas, moderate dialyzability percentages (from 9.0 to 40%) were obtained for bromine species. Iodide and bromide were the major species found in the dialyzates from seaweed, although MIT and bromate were also found in the dialyzates from most of the seaweed samples analysed. However, DIT was only found in dialyzates from Wakame, Kombu, and NIES 09 (Sargasso) certified reference material; whereas, iodate was not found in any dialyzate. Iodine dialyzability was found to be dependent on the protein content (negative correlation), and on the carbohydrate and dietary fibre levels (positive correlation). However, bromine dialyzability was only dependent on the protein amount in seaweed (negative correlation).

  6. Speciation of the bio-available iodine and bromine forms in edible seaweed by high performance liquid chromatography hyphenated with inductively coupled plasma-mass spectrometry

    International Nuclear Information System (INIS)

    Romarís-Hortas, Vanessa; Bermejo-Barrera, Pilar; Moreda-Piñeiro, Jorge; Moreda-Piñeiro, Antonio

    2012-01-01

    Highlights: ► Bioavailable iodine and bromine speciation in edible seaweed were developed. ► In vitro dialyzability was used to assess the bioavailable fractions. ► AEC hyphenated with inductively coupled plasma-mass spectrometry was used. ► Iodide, MIT, DIT, bromide and bromate were found in dialyzates from edible seaweed. ► Positive correlation between bioavailability and protein contents was found. - Abstract: A bioavailability study based on an in vitro dialyzability approach has been applied to assess the bio-available fractions of iodine and bromine species from edible seaweed. Iodide, iodate, 3-iodo-tyrosine (MIT), 3,5-diiodo-tyrosine (DIT), bromide and bromate were separated by anion exchange chromatography under a gradient elution mode (175 mM ammonium nitrate plus 15% (v/v) methanol, pH 3.8, as a mobile phase, and flow rates within the 0.5–1.5 mL min −1 range). Inductively coupled plasma-mass spectrometry (ICP-MS) was used as a selective detector for iodine ( 127 I) and bromine ( 79 Br). Low dialyzability ratios (within the 2.0–18% range) were found for iodine species; whereas, moderate dialyzability percentages (from 9.0 to 40%) were obtained for bromine species. Iodide and bromide were the major species found in the dialyzates from seaweed, although MIT and bromate were also found in the dialyzates from most of the seaweed samples analysed. However, DIT was only found in dialyzates from Wakame, Kombu, and NIES 09 (Sargasso) certified reference material; whereas, iodate was not found in any dialyzate. Iodine dialyzability was found to be dependent on the protein content (negative correlation), and on the carbohydrate and dietary fibre levels (positive correlation). However, bromine dialyzability was only dependent on the protein amount in seaweed (negative correlation).

  7. Production of gaseous tracer I2 from the sodium iodide salt

    International Nuclear Information System (INIS)

    Candeiro, Ricardo E. de M.; Brandao, Luis E. Barreira; Pereira, Wagner do P.

    2009-01-01

    Found in the nature in form different, the iodine has been used in diverse works in the area of the industry and health. The iodine is very unstable and volatile in the ambient temperature and the I 2 is one of the diverse gaseous forms found. In this work was developed methodology for production of gaseous tracer from the sodium iodide (NaI) 0,1 M marked with 123 I. The synthesis was processed with in chlorine acid (HCl) 1M and sodium iodate salt (NaIO 3 ). The production of gas I 2 initially was carried through in unit of glass with the inert material and the purpose was to study the kinetic of reaction. The synthesis occurs in the reaction bottle and the produced gas is stored in the collect bottle that contains a starch solution (5 g/100 mL water). To determine the efficiency of production of gas I 2 , analytic tests had been carried through, where the consumption of iodide ions of the bottle of reaction is measured. The optimization of production of the gaseous tracer was studied varying parameters as: concentration of iodide and iodate, concentration of acid and temperature. Then, the synthesis of the radiotracer was realized in the compact unit, being utilized as main reagent the salt radiated of sodium iodide, Na 123 I. The transportation of elementary iodine was studied by a scintillation detector NaI (2 x 2)'' placed in the reaction bottle. To acquire the data, the detector use a set of electronic modules for the acquisition of signals generated. (author)

  8. The development of written word processing: the case of deaf children The development of written word processing: the case of deaf children

    Directory of Open Access Journals (Sweden)

    Jacqueline Leybaert

    2008-04-01

    Full Text Available Reading is a highly complex, flexible and sophisticated cognitive activity, and word recognition constitutes only a small and limited part of the whole process. It seems however that for various reasons, word recognition is worth studying separately from other components. Considering that writing systems are secondary codes representing the language, word recognition mechanisms may appear as an interface between printed material and general language capabilities, and thus, specific difficulties in reading and spelling acquisition should be iodated at the level of isolated word identification (see e. g. Crowder, 1982 for discussion. Moreover, it appears that a prominent characteristic of poor readers is their lack of efficiency in the processing of isolated words (Mitche11,1982; Stanovich, 1982. And finally, word recognition seems to be a more automatic and less controlled component of the whole reading process. Reading is a highly complex, flexible and sophisticated cognitive activity, and word recognition constitutes only a small and limited part of the whole process. It seems however that for various reasons, word recognition is worth studying separately from other components. Considering that writing systems are secondary codes representing the language, word recognition mechanisms may appear as an interface between printed material and general language capabilities, and thus, specific difficulties in reading and spelling acquisition should be iodated at the level of isolated word identification (see e. g. Crowder, 1982 for discussion. Moreover, it appears that a prominent characteristic of poor readers is their lack of efficiency in the processing of isolated words (Mitche11,1982; Stanovich, 1982. And finally, word recognition seems to be a more automatic and less controlled component of the whole reading process.

  9. Chemical Engineering Division Fuel Cycle Programs. Quarterly progress report, January-March 1979

    Energy Technology Data Exchange (ETDEWEB)

    Steindler, M J; Ader, M; Barletta, R E

    1980-01-01

    In the program on pyrochemical and dry processing methods (PDPM) for nuclear fuel, corrosion testing of refractory metals and alloys, graphite, and SiC in PDPM environments was done. A tungsten-metallized Al/sub 2/O/sub 3/-3% Y/sub 2/O/sub 3/ crucible was successfully fabricated. Tungsten microstructure of a plasma-sprayed tungsten crucible was stabilized by nickel infiltration and heat treatment. Solubility measurements of Th in Cd and Cd-Mg alloys were continued, as were experiments to study the reduction of high-fired ThO/sub 2/. Work on the fused salt electrolysis of CaO also was continued. The method of coprocessing of U and Pu by a salt transport process was modified. Tungsten-coated molybdenum crucibles were fabricated. The proliferation resistance of chloride volatility processing of thorium-based fuels is being evaluated by studying the behavior of fission product elements during chlorination of U and Th. Thermodynamic analysis of the phase relationships in the U-Pu-Zn system was initiated. The Pyro-Civex reprocessing method is being reviewed. Reactivity of UO/sub 2/ and PuO/sub 2/ with molten equimolar NaNO/sub 3/-KNO/sub 3/ is being studied along with the behavior of selected fission product elements. Work was continued on the reprocessing of actinide oxides by extracting the actinides from a bismuth solution. Rate of dissolution of UO/sub 2/ microspheres in LiCl/AlCl/sub 3/ was measured. Nitriding rates of Th and U dissolved in molten tin were measured. In work on the encapsulation of radioactive waste in metal, leach rates of a simulated waste glass were studied. Rates of dissolution of metals (potential barrier materials) in aqueous media are being studied. In work on the transport properties of nuclear waste in geologic media, the adsorption of iodate by hematite as a function of pH and iodate concentration was measured. The migration behavior of cesium in limestone was studied in relation to the cesium concentration and pH of simulated groundwater

  10. Application of quantitative salt iodine analysis compared with the standard method.

    Science.gov (United States)

    Chongchirasiri, S; Pattanachak, S; Putrasreni, N; Suwanik, R; Pattanachak, H; Tojinda, N; Pleehachinda, R

    2001-06-01

    Laboratory investigation of 50 iodated salt samples (from producers, households, markets etc) were studied at the Research Nuclear Medicine Building, Siriraj Hospital. Two methods for the determination of iodine in salt are herein described. The standard method as recommended by The Programme Against Micronutrient Malnutrition (PAMM) / The Micronutrient Initiative (MI)/ The International Council for Control of Iodine Deficiency Disorders (ICCIDD) was the iodometric titration method. The starch-KI salt iodine quantitative method was developed in our laboratory for validation purposes. This method is high in precision, accuracy, sensitivity as well as specificity. The coefficient of variation (%CV) for intra and inter assay was below 10. Iodine contents as low as 10 ppm, could be detected. The proposed starch-KI method offered some advantages: e.g. not complicated, easier to learn and easier to perform competently, could be applied for spot qualitative test and readily performed outside the laboratory. The results obtained by the starch-KI method correlated well with the standard method (y = 0.98x - 3.22, r = 0.99).

  11. Hydrogeochemistry of high iodine groundwater: a case study at the Datong Basin, northern China.

    Science.gov (United States)

    Li, Junxia; Wang, Yanxin; Xie, Xianjun; Zhang, Liping; Guo, Wei

    2013-04-01

    High iodine concentrations in groundwater have seldom been reported and there have been few systematic studies on high iodine groundwater worldwide. To better understand the sources and processes responsible for iodine enrichment in the groundwater of the Datong Basin, the hydrochemical characteristics of groundwater and geochemical features of aquifer sediments were studied. High iodine groundwater mainly occurs in the center of the Datong Basin with iodine concentrations ranging between 3.31 and 1890 μg L(-1). Most samples with iodine concentrations higher than 500 μg L(-1) are from wells with depths between 75 and 120 m. High pH and a reducing environment are favorable for iodine enrichment in the groundwater, with iodide as the dominant species that accounts for 63.2-99.3% of the total iodine. Sediment samples from a borehole specifically drilled for this study contain 0.18-1.46 mg kg(-1) iodine that is moderately correlated with total organic carbon (TOC). The results of sequential extraction experiments show that iodine is mostly bound to iron oxyhydroxides and organic matter in the sediments. The mobilization processes of iodine are proposed to include reductive dissolution of iron oxyhydroxides and transformations among iodide, iodate and organic iodine driven by microbial activities under alkaline and reducing conditions.

  12. Removal efficiency of water purifier and adsorbent for iodine, cesium, strontium, barium and zirconium in drinking water.

    Science.gov (United States)

    Sato, Itaru; Kudo, Hiroaki; Tsuda, Shuji

    2011-01-01

    The severe incident of Fukushima Daiichi Nuclear Power Station has caused radioactive contamination of environment including drinking water. Radioactive iodine, cesium, strontium, barium and zirconium are hazardous fission products because of the high yield and/or relatively long half-life. In the present study, 4 pot-type water purifiers and several adsorbents were examined for the removal effects on these elements from drinking water. Iodide, iodate, cesium and barium were removed by all water purifiers with efficiencies about 85%, 40%, 75-90% and higher than 85%, respectively. These efficiencies lasted for 200 l, which is near the recommended limits for use of filter cartridges, without decay. Strontium was removed with initial efficiencies from 70% to 100%, but the efficiencies were slightly decreased by use. Zirconium was removed by two models, but hardly removed by the other models. Synthetic zeolite A4 efficiently removed cesium, strontium and barium, but had no effect on iodine and zirconium. Natural zeolite, mordenite, removed cesium with an efficiency as high as zeolite A4, but the removal efficiencies for strontium and barium were far less than those of zeolite A4. Activated carbon had little removal effects on these elements. In case of radioactive contamination of tap water, water purifiers may be available for convenient decontamination of drinking water in the home.

  13. Biofortification of lettuce (Lactuca sativa L.) with iodine: the effect of iodine form and concentration in the nutrient solution on growth, development and iodine uptake of lettuce grown in water culture.

    Science.gov (United States)

    Voogt, Wim; Holwerda, Harmen T; Khodabaks, Rashied

    2010-04-15

    Iodine is an essential trace element for humans. Two billion individuals have insufficient iodine intake. Biofortification of vegetables with iodine offers an excellent opportunity to increase iodine intake by humans. The main aim was to study the effect of iodine form and concentration in the nutrient solution on growth, development and iodine uptake of lettuce, grown in water culture. In both a winter and summer trial, dose rates of 0, 13, 39, 65, and 90 or 129 microg iodine L(-1), applied as iodate (IO(3)(-)) or iodide (I(-)), did not affect plant biomass, produce quality or water uptake. Increases in iodine concentration significantly enhanced iodine content in the plant. Iodine contents in plant tissue were up to five times higher with I(-) than with IO(3)(-). Iodine was mainly distributed to the outer leaves. The highest iodide dose rates in both trials resulted in 653 and 764 microg iodine kg(-1) total leaf fresh weight. Biofortification of lettuce with iodine is easily applicable in a hydroponic growing system, both with I(-) and IO(3)(-). I(-) was more effective than IO(3)(-). Fifty grams of iodine-biofortified lettuce would provide, respectively, 22% and 25% of the recommended daily allowance of iodine for adolescents and adults. (c) 2010 Society of Chemical Industry.

  14. An investigation into the effects of maternal supplementation with excess iodine on the mechanisms and impacts of reduced IgG absorption in the lamb postpartum.

    Science.gov (United States)

    McGovern, F M; Sweeney, T; Ryan, M T; Lott, S; Campion, F P; Boland, T M

    2017-04-01

    An experiment was conducted to determine: (1) the effect of excess maternal I supplementation on the thyroid hormone status of the ewe and her progeny; (2) potential mechanisms underpinning the failure of passive transfer associated with excess I and (3) the growing lambs' response to natural gastrointestinal infection. Twin-bearing ewes received one of two treatments (n 32/treatment group): basal diet (C) or C plus 26·6 mg of iodine/ewe per d (I), supplied as calcium iodate. Ewes were individually fed from day 119 of gestation to parturition. Progeny of I ewes had lower (Ph to 28 d postpartum but higher serum IgG concentrations at day 70 postpartum (Plamb at 24 h postpartum; however, thyroid hormone receptor-β (THRB) and β-2-microglobulin (B2M) expression declined (Plamb postpartum. These effects were followed by an enhancement of average daily gain and lower N. battus FEC in the pre-weaning period of I-supplemented lambs.

  15. The use of 125iodine-labeled RNA for detection of the RNA binding to ribosomes

    International Nuclear Information System (INIS)

    Mori, Tomohiko; Fukuda, Mitsuru

    1975-01-01

    The in vitro labeling of RNA with radioactive iodine is the efficient method to obtain the RNA with high specific activity. The present paper reports on the application of this technique to the production of iodine-labeled RNA for use in the experiment of binding RNA to ribosomes. Tobacco mosaic virus (TMV) RNA was used as natural mRNA, and E. coli S-30 preparation was used as a source of ribosomes. The TMV-RNA was prepared by bentonite-phenol extraction from TMV, and the method used for the iodation of RNA was based on the procedure described by Getz et al. The iodine-labeled RNA was incubated in a cell-free protein synthesizing system (S-30) prepared from E. coli K-12. After the incubation, the reaction mixture was layered onto sucrose gradient, centrifuged, and fractionated into 18 fractions. Optical density at 260 nm was measured, and radioactivity was counted, for each fraction. The binding of mRNA to ribosomes occurred even at 0 deg C, and the occurrence of the nonspecific binding was also shown. Consequently, the specific binding, i.e. the formation of the initiation complex being involved in amino acid incorporation, may be estimated by subtracting the radioactivity associated with monosomes in the presence of both rRNA and ATA from that in the presence of rRNA only. It was shown that the iodine-labeled RNA can be used for the studies of binding RNA to ribosomes. (Kako, I.)

  16. Status of radioiodine control for nuclear fuel reprocessing plants

    International Nuclear Information System (INIS)

    Burger, L.L.; Scheele, R.D.

    1983-07-01

    This report summarizes the status of radioiodine control in a nuclear fuel reprocessing plant with respect to capture, fixation, and disposal. Where possible, we refer the reader to a number of survey documents which have been published in the last four years. We provide updates where necessary. Also discussed are factors which must be considered in developing criteria for iodine control. For capture from gas streams, silver mordenite and a silver nitrate impregnated silica (AC-6120) are considered state-of-the-art and are recommended. Three aqueous scrubbing processes have been demonstrated: Caustic scrubbing is simple but probably will not give an adequate iodine retention by itself. Mercurex (mercuric nitrate-nitric acid scrubbing) has a number of disadvantages including the use of toxic mercury. Iodox (hyperazeotropic nitric acid scrubbing) is effective but employs a very corrosive and hazardous material. Other technologies have been tested but require extensive development. The waste forms recommended for long-term storage or disposal are silver iodide, the iodates of barium, strontium, or calcium, and silver loaded sorbents, all fixed in cement. Copper iodide in bitumen (asphalt) is a possibility but requires testing. The selection of a specific form will be influenced by the capture process used

  17. Calcium-independent phospholipase A₂, group VIA, is critical for RPE cell survival

    DEFF Research Database (Denmark)

    Kolko, Miriam; Vohra, Rupali; Westlund, Barbro S.

    2014-01-01

    PURPOSE: To investigate the significance of calcium-independent phospholipase A₂, group VIA (iPLA2-VIA), in RPE cell survival following responses to sodium iodate (SI) in cell cultures. METHODS: The human retinal pigment epithelium (RPE) cell line (ARPE-19) cells and primary mouse-RPE cultures we......-induced RPE cell death can be facilitated by inhibitors of iPLA₂-VIA. Thus, we suggest iPLA₂-VIA as a possible pharmaceutical target to treat RPE-related retinal diseases....... treated with SI to induce cell death. Cells were transfected with an iPLA₂-VIA promoter-luciferase construct to evaluate the regulation of iPLA-VIA after exposure to SI. PCR analysis, western blot analysis, and activity assays were performed to evaluate the mRNA level, protein level, and activity levels...... of iPLA₂-VIA after SI exposure. Inhibitors of iPLA₂-VIA were used to explore a potential protective role in cells exposed to SI. Primary RPE cell cultures were grown from iPLA₂-VIA knockout mice and wild-type mice. The cultures were exposed to SI to investigate a possible increased protection against...

  18. Synthetic approach of norbadione A: new preparation of alcohols from sulfones and boron compounds

    International Nuclear Information System (INIS)

    Billaud, C.

    2005-12-01

    The synthetic approach of norbadione A, a pigment from mushrooms related to pulvinic acids, was studied. This compound has the property to complex caesium and has shown an antioxidant activity. The first strategy, based on a double Suzuki-Miyaura coupling between a naphtho-lactone with two boron functions and two pulvinic moieties with a triflate was unsuccessful and has shown a deactivating effect of the lactone. Modifications aimed to inhibit the electro-attracting character of the lactone permitted to obtain a bis(coupled) product with a poor yield. A second approach based on a the cyclization of enol aryl-acetates was studied in order to build the pulvinic moiety in several steps. The important reaction of introduction of an alkyl-acetate from a triflate was realised by a palladium-mediated coupling. The cyclization attempts carried out using a naphthalenic compound allowed us to isolate a monocyclised product. A parallel study was to first build a tetronic moiety and then to construct the exocyclic double bond by a method developed in the laboratory for the preparation of an iodated pulvinic compound. Finally, a new preparation of alcohols from sulfones and boron compounds was developed. Two known reactions in the chemistry of boron were combined. The first one is the reaction between anions of sulfones and tri-alkyl-boranes, the second one is a thermal isomerization which places the boron atom in a terminal position. A new preparation of primary alcohols was thus carried out. (author)

  19. Extraction of long-lived radionuclides from caustic Hanford tank waste supernatants

    Energy Technology Data Exchange (ETDEWEB)

    Chaiko, D.J.; Mertz, C.J.; Vojta, Y. [and others

    1995-07-01

    A series of polymer-based extraction systems, based on the use of polyethylene glycols (PEGs) or polypropylene glycols (PPGs), was demonstrated to be capable of selective extraction and recovery of long-lived radionuclides, such as {sup 99}Tc and {sup 129}I, from Hanford SY-101 tank waste, neutralized current acid waste, and single-shell tank waste simulants. During the extraction process, anionic species like TcO{sub 4}{sup {minus}} and I{sup {minus}} are selectively transferred to the less dense PEG-rich aqueous phase. The partition coefficients for a wide range of inorganic cations and anions, such as sodium, potassium, aluminum, nitrate, nitrite, and carbonate, are all less than one. The partition coefficients for pertechnetate ranged from 12 to 50, depending on the choice of waste simulant and temperature. The partition coefficient for iodide was about 5, while that of iodate was about 0.25. Irradiation of the PEG phase with gamma-ray doses up to 20 Mrad had no detectable effect on the partition coefficients. The most selective extraction systems examined were those based on PPGs, which exhibited separation factors in excess of 3000 between TcO{sub 4}{sup {minus}} and NO{sub 3}{sup {minus}}/NO{sub 2}{sub {minus}}. An advantage of the PPG-based system is minimization of secondary waste production. These studies also highlighted the need for exercising great care in extrapolating the partitioning behavior with tank waste simulants to actual tank waste.

  20. Silver iodide reduction in aqueous solution: application to iodine enhanced separation during spent nuclear fuels reprocessing

    International Nuclear Information System (INIS)

    Badie, Jerome

    2002-01-01

    Silver iodide is a key-compound in nuclear chemistry either in accidental conditions or during the reprocessing of spent nuclear fuel. In that case, the major part of iodine is released in molecular form into the gaseous phase at the time of dissolution in nitric acid. In French reprocessing plants, iodine is trapped in the dissolver off-gas treatment unit by two successive steps: the first consists in absorption by scrubbing with a caustic soda solution and in the second, residual iodine is removed from the gaseous stream before the stack by chemisorption on mineral porous traps made up of beds of amorphous silica or alumina porous balls impregnated with silver nitrate. Reactions of iodine species with the impregnant are assumed to lead to silver iodide and silver iodate. Enhanced separation policy would make necessary to recover iodine from the filters by silver iodide dissolution during a reducing treatment. After a brief silver-iodine chemical bibliographic review, the possible reagents listed in the literature were studied. The choice has been made to use ascorbic acid and hydroxylamine. An experimental work on silver iodide reduction by this two compounds allowed us to determinate reaction products, stoichiometry and kinetics parameters. Finally, the process has been initiated on stable iodine loaded filters samples. (author) [fr

  1. Temperature-dependent adsorption of surfactant molecules and associated crystallization kinetics of noncentrosymmetric Fe(IO{sub 3}){sub 3} nanorods in microemulsions

    Energy Technology Data Exchange (ETDEWEB)

    El-Kass, Moustafa [Université de Savoie, Laboratoire SYMME, BP 80439, 74944 Annecy Le Vieux Cedex (France); Ladj, Rachid [Université de Savoie, Laboratoire SYMME, BP 80439, 74944 Annecy Le Vieux Cedex (France); Université Lyon1, CNRS, UMR 5007, LAGEP, CPE, 43 bd 11 Novembre 1918, F-69622 Villeurbanne (France); Mugnier, Yannick, E-mail: Yannick.Mugnier@univ-savoie.fr [Université de Savoie, Laboratoire SYMME, BP 80439, 74944 Annecy Le Vieux Cedex (France); Le Dantec, Ronan [Université de Savoie, Laboratoire SYMME, BP 80439, 74944 Annecy Le Vieux Cedex (France); Hadji, Rachid [Institut Jean Lamour, UMR CNRS n°7198, Université de Lorraine, Nancy 1, BP 239, 54506 Vandoeuvre-lès-Nancy Cedex (France); Marty, Jean-Christophe [Université de Savoie, Laboratoire SYMME, BP 80439, 74944 Annecy Le Vieux Cedex (France); Rouxel, Didier [Institut Jean Lamour, UMR CNRS n°7198, Université de Lorraine, Nancy 1, BP 239, 54506 Vandoeuvre-lès-Nancy Cedex (France); Durand, Christiane [Université de Savoie, Laboratoire SYMME, BP 80439, 74944 Annecy Le Vieux Cedex (France); Fontvieille, Dominique [UMR CARRTEL (INRA/Université de Savoie), Laboratoire de Microbiologie Aquatique, BP 511, 74203 Thonon Cedex (France); Rogalska, Ewa [Structure et Réactivité des Systèmes Moléculaires Complexes, UMR 7565, Nancy Université, BP 70239, 54506 Vandoeuvre-lès-Nancy cedex (France); and others

    2013-11-15

    Graphical abstract: - Highlights: • Crystallization of Fe(IO{sub 3}){sub 3} in microemulsions probed by hyper-Rayleigh scattering. • A faster growth and a better shape control of nanorods are obtained at 80 °C. • Different persistent cell deformations are related to the crystallization kinetics. • A temperature-dependent adsorption of surfactants on nanorods is suggested. - Abstract: Aggregation-induced crystallization of iron iodate nanorods within organic–inorganic aggregates of primary amorphous precursors is probed by time-dependent hyper-Rayleigh scattering measurements in Triton X-100 based-microemulsions. In the context of a growing interest of noncentrosymmetric oxide nanomaterials in multi-photon bioimaging, we demonstrate by a combination of X-ray diffraction and electron microscopy that an increase in the synthesis of temperature results in faster crystallization kinetics and in a better shape-control of the final Fe(IO{sub 3}){sub 3} nanorods. For initial microemulsions of fixed composition, room-temperature synthesis leads to bundles of 1–3 μm long nanorods, whereas shorter individual nanorods are obtained when the temperature is increased. Results are interpreted in terms of kinetically unfavorable mesoscale transformations due to the strong binding interactions with Triton molecules. The interplay between the nanorod crystallization kinetics and their corresponding unit cell deformation, evidenced by lattice parameter refinements, is attributed to a temperature-dependent adsorption of surfactants molecules at the organic–inorganic interface.

  2. The kinetic study of oxidation of iodine by hydrogen peroxide

    International Nuclear Information System (INIS)

    Cantrel, L.; Chopin, J.

    1996-01-01

    Iodine chemistry is one of the most important subjects of research in the field of reactor safety because this element can form volatile species which represent a biological hazard for environment. As the iodine and the peroxide are both present in the sump of the containment in the event of a severe accident on a light water nuclear reactor, it can be important to improve the knowledge on the reaction of oxidation of iodine by hydrogen peroxide. The kinetics of iodine by hydrogen peroxide has been studied in acid solution using two different analytical methods. The first is a UV/Vis spectrophotometer which records the transmitted intensity at 460 nm as a function of time to follow the decrease of iodine concentration, the second is an amperometric method which permits to record the increase of iodine+1 with time thanks to the current of reduction of iodine+1 to molecular iodine. The iodine was generated by Dushman reaction and the series of investigations were made at 40 o C in a continuous stirring tank reactor. The influence of the initial concentrations of iodine, iodate, hydrogen peroxide, H + ions has been determined. The kinetics curves comprise two distinct chemical phases both for molecular iodine and for iodine+1. The relative importance of the two processes is connected to the initial concentrations of [I 2 ], [IO 3 - ], [H 2 O 2 ] and [H + ]. A rate law has been determined for the two steps for molecular iodine. (author) figs., tabs., 22 refs

  3. A New Technology Developed to Remove Aqueous Radioiodine

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Seung Yeop; Baik, Min Hoon [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2015-10-15

    Radioiodine is considered as a critical radionuclide by the International Commission on Radiological Protection(ICRP) in terms of the radiation and radiotoxicity risks to nature and human health. In addition, there were reports about great increases of thyroid cancer in children in Belarus from 1990. In natural environments, there were several reports for the unusual increase of radioactive iodine ratios in most environmental samples (i.e. soils, vegetables, and seafoods). Iodine usually exists as iodide, iodate, and organic iodine in the environment. Iodide is considered as the most difficult form among the iodine species to treat by the conventional adsorption-based technology. This is why urgent new technology is needed to suppress such a progressive accumulation of radioiodine in natural environments. The conventional methods based on the anion-exchange and adsorption techniques have been difficult to manage the growing release of radioiodine for decades. Here we suggest a new solution that uses a biostimulant way to isolate radioiodine. We discovered that natural SRB can play an important intermediary role to get anionic iodide and cationic copper combined strongly as perfect counterions by enzymatic Cu-reduction.

  4. Chemical state and distribution of iodine deposits on 17% Cr/12% Ni steel oxidised in CO2/CH3I gas mixtures

    International Nuclear Information System (INIS)

    Allen, G.C.; Tyler, J.W.

    1990-01-01

    Iodine-131 is one of the most important volatile fission product elements with respect to radiobiological impact, and the characterisation of its chemical state and distribution on reactor surfaces is required for reactor safety assessments. To this end, duplicate samples of Type 316 (17% Cr/12% Ni) stainless steel oxidised in CO 2 /CH 3 I gas mixtures and previously characterised using X-ray photoelectron spectroscopy have been examined using Raman spectroscopy. The aim is to improve our understanding of the way in which iodine is distributed throughout the oxide scale and to identify its chemical state. In this paper we present Raman spectra recorded from a series of stainless steel specimens together with spectra recorded from a number of standard iodine compounds. It is demonstrated that the technique is well suited as a fingerprint method of species identification, can differentiate between the chemical state of iodine as iodide and iodate and can analyse thin oxide films (5-50 nm). Identification of iodine deposits in these oxide films at concentrations of ≤2 at% was not achieved however, there being insufficient iodine present to distinguish any peaks present from the background signal. It is concluded that local concentrations of iodine in oxide inclusions of different composition/morphology on the steel surface does not occur to any extent. (orig.)

  5. Chitosan finishing nonwoven textiles loaded with silver and iodide for antibacterial wound dressing applications.

    Science.gov (United States)

    Aubert-Viard, François; Martin, Adeline; Chai, Feng; Neut, Christel; Tabary, Nicolas; Martel, Bernard; Blanchemain, Nicolas

    2015-03-02

    Polyethylene terephtalate (PET) and Polypropylene (PP) textiles are widely used in biomedical application such as wound dressings and implants. The aim of this work was to develop an antibacterial chitosan (CHT) coating activated by silver or by iodine. Chitosan was immobilized onto PET and PP supports using citric acid (CTR) as a crosslinking agent through a pad-dry-cure textile finishing process. Interestingly, depending on the CHT/CTR molar ratio, two different systems were obtained: rich in cationic ammonium groups when the CTR concentration was 1%w/v, and rich in anionic carboxylate groups when the CTR concentration was 10%w/v. As a consequence, such samples could be selectively loaded with iodine and silver nitrate, respectively.Both types of coatings were analyzed using SEM and FTIR, their sorption capacities were evaluated toward iodide/iodate anions (I(-)/IO3(-)) and the silver cations (Ag(+)) were evaluated using elemental analysis. Finally, in vitro evaluations were carried out to evaluate the cytocompatibility on the epithelial cell line. The silver loaded textile reported a stronger antibacterial effect against E.coli (5 log10 reduction) than toward S. aureus (3 log10) while the antibacterial effect of the iodide loaded textiles was limited to 1 log10 to 2 log10 on both strains.

  6. An assessment of Raman spectroscopy to detect iodine deposited on thin oxide films formed on Type 316 stainless steel

    International Nuclear Information System (INIS)

    Allen, G.C.; Tyler, J.W.

    1989-04-01

    Iodine-131 is one of the most important volatile fission product elements with respect to radiobiological impact, and the characterisation of its chemical state and distribution on reactor surfaces is required for reactor safety assessments. To this end, duplicate samples of Type 316 (17%Cr/12%Ni) stainless steel oxidised in Co 2 /CH 3 I gas mixtures and previously characterised using X-ray photoelectron spectroscopy have been examined using Raman spectroscopy. The aim is to improve our understanding of the way in which iodine is distributed throughout the oxide scale and to identify its chemical state. In this report we present Raman spectra recorded from a series of stainless steel specimens together with spectra recorded from a number of standard iodine compounds. It is demonstrated that the technique is well suited as a fingerprint method of species identification, can differentiate between the chemical state of iodine as iodide and iodate and can analyse thin oxide films (5-50 nm). Identification of iodine deposits in these oxide films at concentrations of ≤1 At% was not achieved however, there being insufficient iodine present to distinguish any peaks present from the background signal. It is concluded that local concentrations of iodine in oxide inclusions of different composition/morphology on the steel surface does not occur to any extent. (author)

  7. The kinetics of iodide oxidation by the manganese oxide mineral birnessite

    Science.gov (United States)

    Fox, P.M.; Davis, J.A.; Luther, G. W.

    2009-01-01

    The kinetics of iodide (I-) and molecular iodine (I2) oxidation by the manganese oxide mineral birnessite (??-MnO2) was investigated over the pH range 4.5-6.25. I- oxidation to iodate (IO3-) proceeded as a two-step reaction through an I2 intermediate. The rate of the reaction varied with both pH and birnessite concentration, with faster oxidation occurring at lower pH and higher birnessite concentration. The disappearance of I- from solution was first order with respect to I- concentration, pH, and birnessite concentration, such that -d[I-]/dt = k[I-][H+][MnO2], where k, the third order rate constant, is equal to 1.08 ?? 0.06 ?? 107 M-2 h-1. The data are consistent with the formation of an inner sphere I- surface complex as the first step of the reaction, and the adsorption of I- exhibited significant pH dependence. Both I2, and to a lesser extent, IO3- sorbed to birnessite. The results indicate that iodine transport in mildly acidic groundwater systems may not be conservative. Because of the higher adsorption of the oxidized I species I2 and IO3-, as well as the biophilic nature of I2, redox transformations of iodine must be taken into account when predicting I transport in aquifers and watersheds.

  8. A novel vortex-assisted liquid-liquid microextraction approach using auxiliary solvent: Determination of iodide in mineral water samples.

    Science.gov (United States)

    Zaruba, Serhii; Vishnikin, Andriy B; Andruch, Vasil

    2016-01-01

    A novel vortex-assisted liquid-liquid microextraction (VA-LLME) for determination of iodide was developed. The method includes the oxidation of iodide with iodate in the presence of hydrochloric acid followed by VA-LLME of the ion-pair formed between ICl2(-) and Astra Phloxine reagent (AP) and subsequent absorbance measurement at 555nm. The appropriate experimental conditions were investigated and found to be: 5mL of sample, 0.27molL(-)(1) HCl, 0.027mmolL(-1) KIO3 as the oxidation agent, 250μL of extraction mixture containing amyl acetate as the extraction solvent and carbon tetrachloride as the auxiliary solvent (1:1, v/v), 0.04mmolL(-1) AP reagent, vortex time: 20s at 3000rpm, centrifugation: 4min at 3000rpm. The calibration plot was linear in the range 16.9-169μg L(-1) of iodide, with a correlation coefficient (R(2)) of 0.996, and the relative standard deviation ranged from 1.9 to 5.7%. The limit of detection (LOD) and limit of quantification (LOQ) were 1.75 and 6.01μgL(-)(1) of iodide, respectively. The suggested procedure was applied for determination of iodide in real mineral water samples. Copyright © 2015 Elsevier B.V. All rights reserved.

  9. Optimized and Validated Spectrophotometric Methods for the Determination of Enalapril Maleate in Commercial Dosage Forms

    Directory of Open Access Journals (Sweden)

    Sk Manirul Haque

    2008-01-01

    Full Text Available Four simple, rapid and sensitive spectrophotometric methods have been proposed for the determination of enalapril maleate in pharmaceutical formulations. The first method is based on the reaction of carboxylic acid group of enalapril maleate with a mixture of potassium iodate (KIO3 and iodide (KI to form yellow colored product in aqueous medium at 25 ± 1°C .The reaction is followed spectrophotometrically by measuring the absorbance at 352 nm. The second, third and fourth methods are based on the charge transfer complexation reaction of the drug with p-chloranilic acid (pCA in 1, 4-dioxan-methanol medium, 2, 3-dichloro 5, 6-dicyano 1, 4-benzoquinone (DDQ in acetonitrile-1,4 dioxane medium and iodine in acetonitrile-dichloromethane medium. Under optimized experimental conditions, Beer’s law is obeyed in the concentration ranges of 2.5–50, 20–560, 5–75 and 10–200 μg mL−1, respectively. All the methods have been applied to the determination of enalapril maleate in pharmaceutical dosage forms. Results of analysis are validated statistically.

  10. Optimized and validated spectrophotometric methods for the determination of enalapril maleate in commercial dosage forms.

    Science.gov (United States)

    Rahman, Nafisur; Haque, Sk Manirul

    2008-03-01

    Four simple, rapid and sensitive spectrophotometric methods have been proposed for the determination of enalapril maleate in pharmaceutical formulations. The first method is based on the reaction of carboxylic acid group of enalapril maleate with a mixture of potassium iodate (KIO(3)) and iodide (KI) to form yellow colored product in aqueous medium at 25 +/- 1 degrees C. The reaction is followed spectrophotometrically by measuring the absorbance at 352 nm. The second, third and fourth methods are based on the charge transfer complexation reaction of the drug with p-chloranilic acid (pCA) in 1, 4-dioxan-methanol medium, 2, 3-dichloro 5, 6-dicyano 1, 4-benzoquinone (DDQ) in acetonitrile-1,4 dioxane medium and iodine in acetonitrile-dichloromethane medium. Under optimized experimental conditions, Beer's law is obeyed in the concentration ranges of 2.5-50, 20-560, 5-75 and 10-200 microg mL(-1), respectively. All the methods have been applied to the determination of enalapril maleate in pharmaceutical dosage forms. Results of analysis are validated statistically.

  11. On-the-fly green generation and dispersion of AgI nanoparticles for cloud seeding nuclei

    Energy Technology Data Exchange (ETDEWEB)

    Hu, Xiuli; Zhou, Wenbo; Wang, Xizheng; Wu, Tao; Delisio, Jeffery B.; Zachariah, Michael R., E-mail: mrz@umd.edu [University of Maryland, Department of Chemical and Biomolecular Engineering (United States)

    2016-07-15

    This study reports on an on-the-fly green synthesis/dispersion of silver iodide (AgI) nanoparticles from the combustion of AgIO{sub 3}/carbon black (CB)/nitrocellulose (NC) composites, which could be used as a candidate for a cloud-seeding pyrotechnic. Films were formed by direct electrospray deposition of a mixture of synthesized silver iodate with CB and NC. The decomposition pathways of AgIO{sub 3}/CB and AgIO{sub 3}/CB/NC were evaluated by temperature jump time of flight mass spectrometry (T-jump TOFMS) and XRD, showing that AgI particles and CO{sub 2} are released from the reaction between AgIO{sub 3} and CB without other toxic residuals. The flame propagation velocity of AgIO{sub 3}/CB/NC films increases with the increasing of particle mass loading of AgIO{sub 3} and CB and peaks at 40 wt%, which is much higher than that of an AgI/AP/NC film. The mean diameter of the resultant AgI nanoparticles is from 51 to 97 nm. The mass loading of AgIO{sub 3} and CB was found to play a major role in size control of the AgI nanoparticles.

  12. Ontario is not ready to face a large-scale nuclear accident

    International Nuclear Information System (INIS)

    2017-07-01

    On paper, in Japan as elsewhere, nuclear emergency plans are based on international standards and all look similar. The counter measures are sheltering, potassium iodate prophylaxis, evacuation and control of foodstuffs. With 18 nuclear reactors to produce electricity and a research reactor, Ontario should be especially well prepared. Moreover, in USA, there are six power plants located at less than 100 km from the Canadian border. Would Ontario do better than Japan in case of a severe nuclear disaster? Ontario is not ready to face a severe nuclear accident and the population surrounding nuclear power stations are at risk. The large number of inhabitants will hamper protective response actions. Consequently, Canadian authorities keep lax protective action levels. Using more stringent levels would mean to extend the protection zone that would include a too large number of persons. Canadian authorities should openly acknowledge that a severe nuclear accident could happen in Ontario like in any other country and trigger a complete reorganisation of emergency preparedness and response (EP and R) to cope with such a possibility. New response plans should be defined with the involvement of stakeholders

  13. Selective determination of penicillamine by on-line vapor-phase generation combined with Fourier transform infrared spectrometry.

    Science.gov (United States)

    Zeeb, Mohsen; Ganjali, Mohammad Reza; Norouzi, Parviz; Moeinossadat, Seyyed Rezvan

    2009-04-30

    In this work, an on-line system with vapor-phase generation (VPG) and Fourier transform infrared (FTIR) spectrometric detection has been developed as a direct and highly selective analytical technique for the assay of penicillamine (PA). Potassium iodate solution was injected into a reactor, heated at 75 degrees C, containing PA. The CO generated under these conditions was transported by means of N(2) gas carrier stream to an infrared gas cell and corresponding FTIR spectra were acquired in a continuous mode. The maximum absorbance of CO band at 2170 cm(-1), corrected by a baseline established between 2240 and 2000 cm(-1) at a nominal resolution of 2 cm(-1), was selected as a measurement criterion. Initially, the effect of different chemical, physical and spectroscopic parameters, such as concentration and volume of oxidant, pH, equilibrium time, reactor temperature, reactor volume, N(2) carrier flow rate and number of scans on the analytical signals were evaluated by using a short path length (10 cm) IR gas cell. At optimum experimental conditions, the method provided a relatively broad linear dynamic range of 4-380 mg L(-1), a limit of detection of 0.5 mg L(-1), a sampling frequency of 15 h(-1) and a relative standard deviation (R.S.D.) of 1.6%. Further, the method was successfully applied to the determination of PA in pharmaceutical formulations and results compared well with those obtained by a reference colorimetric method.

  14. Volatilization: a soil degassing coefficient for iodine

    International Nuclear Information System (INIS)

    Sheppard, M.I.; Thibault, D.H.; Smith, P.A.; Hawkins, J.L.

    1994-01-01

    Iodine, an element essential to some animals, is ubiquitous in the biosphere. Unlike other metallic elements, molecular I is volatile, and other inorganic species present in aerated soils, such as I - and IO 3 - , may also volatilize as hydrides, hydrogen iodide (HI), or hydrogen iodates (HIO 3 , HIO 4 ). Methyl iodide has been measured in soils, and it is likely evolved from soils and plants. The long-lived radioisotope 129 I is abundant in nuclear wastes, and its high solubility in groundwater makes it an important element in the performance assessment of underground disposal facilities. Overestimates of soil I residence half-times by traditional foodchain models may be due to underestimation of volatilization. Field and lysimeter experiments over a 3-year period, and direct trapping experiments in the laboratory are reported. The results, combined with values from the literature, indicate the soil I degassing coefficient for a wide range of soil types, vegetated and bare, wet and dry, is lognormally distributed with a geometric mean of 2.1 x 10 -2 year -1 , a range of 1.8 x 10 -4 to 3.1 year -1 and a geometric standard deviation of 3.0. The results of a biosphere model simulation including degassing reduces soil I concentrations fivefold and increases air concentrations 25-fold at steady state, compared to simulations without degassing. (author)

  15. Charge transport mechanism and low temperature phase transitions in KIO3

    Science.gov (United States)

    Abdel Kader, M. M.; El-Kabbany, F.; Naguib, H. M.; Gamal, W. M.

    2013-04-01

    Our report deals with the measurement of some electrical properties, namely the ac conductivity σ(ω,T) and the complex dielectric permittivity epsilon*(ω, T) in the temperature interval 95K < T < 280K and at some selected frequencies (0.7kHz - 20kHz) for polycrystalline samples of potassium iodate KIO3 using a computerized RLC meter. The improper character of the ferroelectricity over the mentioned temperature range has been achieved by recording the ferroelectric hysteresis loops. The temperature dependence of each electrical parameter reveals that the compound undergoes two phase transitions at T ≈ 258K and at T ≈ 110K. The frequency dependent conductivity seems to be in accordance with the power law σ(ω,T)αωs(T) and the trend of temperature dependence of the frequency exponent s (0 < s < 1) suggests that the quantum mechanical tunneling (QMT) model is the main mechanism of the charge transport. Comparison with the behavior of the NH4IO3 in the same temperature range was outlined.

  16. Site-dependent charge transfer at the Pt(111)-ZnPc interface and the effect of iodine

    International Nuclear Information System (INIS)

    Ahmadi, Sareh; Wojek, Bastian M.; Noël, Quentin; Göthelid, Mats; Agnarsson, Björn; Bidermane, Ieva; Sun, Chenghua

    2014-01-01

    The electronic structure of ZnPc, from sub-monolayers to thick films, on bare and iodated Pt(111) is studied by means of X-ray photoelectron spectroscopy, X-ray absorption spectroscopy, and scanning tunneling microscopy. Our results suggest that at low coverage ZnPc lies almost parallel to the Pt(111) substrate, in a non-planar configuration induced by Zn-Pt attraction, leading to an inhomogeneous charge distribution within the molecule and an inhomogeneous charge transfer to the molecule. ZnPc does not form a complete monolayer on the Pt surface, due to a surface-mediated intermolecular repulsion. At higher coverage ZnPc adopts a tilted geometry, due to a reduced molecule-substrate interaction. Our photoemission results illustrate that ZnPc is practically decoupled from Pt, already from the second layer. Pre-deposition of iodine on Pt hinders the Zn-Pt attraction, leading to a non-distorted first layer ZnPc in contact with Pt(111)-I(√3×√3) or Pt(111)-I(√7×√7), and a more homogeneous charge distribution and charge transfer at the interface. On increased ZnPc thickness iodine is dissolved in the organic film where it acts as an electron acceptor dopant

  17. Iodized salt supplementation and its effects on thyroid status amongst Orang Asli in Hulu Selangor, Malaysia.

    Science.gov (United States)

    Lim, Kuang Kuay; Wong, Ming; Mohamud, Wan Nazaimoon Wan; Kamaruddin, Nor Azmi

    2013-01-01

    This research was performed to determine the prevalence of iodine deficiency disorder (IDD) and the effects of iodized salt supplementation on thyroid status amongst Orang Asli in Hulu Selangor, Malaysia. Study respondents were from three target groups, i.e. pre-school children (PSC), primary school-going children (SGC) and adult women. Each household was supplied with iodized salt fortified with iodate fortificant for a period of 12 months and the iodine levels in the salt ranged from 20 to 30 μg/L. Samples collected before and after 6 and 12 months of introduction to iodized salt were urine from all groups, as well as serum samples from adult women. A total of 200 respondents were recruited; 58 (29.0%) PSC, 65 (32.5%) SGC and 77 (38.5%) adult women. The median urine-iodine concentration (mUIC) in all groups were of moderately low before the iodized salt intervention, but increased significantly in all study groups after 6 and 12 months of intervention. However, at the end of the study, there was an increase in severe iodine deficiency (mUIC Orang Asli. However, an increase in severe iodine deficiency and iodine excess indicated that the iodized salt programme needs to be carefully monitored.

  18. A review of methods for immobilizing iodine-129 arising from a nuclear fuel recycle plant, with emphasis on waste-form chemistry

    International Nuclear Information System (INIS)

    Taylor, P.

    1990-07-01

    Possible methods for the separation and immobilization of iodine (mainly iodine-129) in a fuel recycle plant are reviewed, with special emphasis placed on the evaluation of waste forms. A distinction is drawn between waste forms selected by thermodynamic (solubility) or kinetic (dissolution rate) considerations. The most promising solubility-limited waste forms appear to be AgI (or AgI + AgCl) and a combination of Bi 2 O 3 and Bi 5 O 7 I. These materials use relatively scarce metals, Ag and Bi. They also have substantial chemical limitations, such as susceptibility to reductive dissolution and anion-displacement reactions; this calls for special care in the choice of a disposal site. All other organic iodides and iodates considered here and elsewhere appear to be still more limited in this respect. The most promising kinetically limited candidate waste form appears to be iodide-sodalite, but further information is needed on both the fabrication and leaching behaviour of this material. The possibility of disposal in a more soluble but isotopically dilute waste form, employing abundant raw materials, also warrants further consideration

  19. Hydrothermal synthesis of C3N4/BiOIO3 heterostructures with enhanced photocatalytic properties.

    Science.gov (United States)

    Wang, Wenjun; Cheng, Hefeng; Huang, Baibiao; Liu, Xiaolei; Qin, Xiaoyan; Zhang, Xiaoyang; Dai, Ying

    2015-03-15

    The C3N4/BiOIO3 composites with heterostructures have been fabricated by simply depositing BiOIO3 on the surface of C3N4 at hydrothermal conditions, using bismuth nitrate and potassium iodate as precursors. C3N4 is an excellent organic semiconductor, which can be excited by visible light. BiOIO3 is a layered bismuth-based compound that has an internal polar field. Coupling C3N4 with BiOIO3 can combine the advantages of the two compounds and obtain better photocatalytic properties. X-ray diffraction, scanning electron microscopy, transmission electron microscopy and Fourier transformation infrared spectra have been carried out to confirm the structures and morphologies of as-prepared products. The absorption properties have been characterized by diffuse reflectance spectra and the photocatalytic activities have been evaluated by photodegradation of methyl orange, Rhodamine B and 2,4-dichlorophenol. Compared with C3N4, all C3N4/BiOIO3 composites exhibit better visible-light-driven photocatalytic properties. It is a synergetic effect that enables the composites to harvest light and promote charge separation, which eventually leads to the enhancement of the photocatalytic efficiencies. Under UV-vis light irradiation, C3N4/BiOIO3 composites also exhibit better activities, and the charge transfer process is similar to a redox mediator-free Z-scheme system. Copyright © 2014 Elsevier Inc. All rights reserved.

  20. Evaluation of antioxidant activity of some natural polyphenolic compounds using the Briggs-Rauscher reaction method.

    Science.gov (United States)

    Cervellati, Rinaldo; Renzulli, Cecilia; Guerra, Maria Clelia; Speroni, Ester

    2002-12-18

    A new method based on the inhibitory effects of antioxidants on the oscillations of the hydrogen peroxide, acidic iodate, malonic acid, and Mn(II)-catalyzed system (known as the Briggs-Rauscher reaction), was used for the evaluation of antioxidative capacity. With this method, which works near the pH of the fluids in the stomach (pH approximately 2), a group of natural compounds present in fruits and vegetables or in medicinal plants assumed to have antioxidant capacity, was tested successfully. The aim of the present study is to evaluate the antioxidative properties of some active principles contained in vegetables and aromatic plants, namely, cynarin (from Cynara scolymus), rosmarinic acid (from Rosmarinus officinalis), echinacoside (from Echinacea species), puerarin (from Pueraria lobata), and oleuropein (from Olea europea). Also studied with the Briggs-Rauscher reaction method was the antioxidant activity of cyanidin 3-O-beta-glucopyranoside (from Citrus aurantium) in order to compare the results with those obtained by other methods. The conclusions on the dependency of the antioxidative activity on the pH of the testing system are given.

  1. Actinometric and biodosimetric evaluation of UV-C dose delivery in annular, Taylor-Coutte and coiled tube continuous systems.

    Science.gov (United States)

    Müller, Alexandra; Orlowska, Marta; Knörr, Michael; Stahl, Mario R; Greiner, Ralf; Koutchma, Tatiana

    2017-04-01

    In this study, the evaluation of the performance of two thin-film UV-C reactors (annular and Taylor-Couette) and a coiled tube system is presented using actinometry and biodosimetry methods. The iodide/iodate actinometry method was found suitable for comparison of the efficiency of UV-C dose delivery of the UV-C continuous flow systems. Inactivation kinetics of Escherichia coli ATCC 8739 in quarter-strength Ringer's solution (absorption coefficient α 254 nm  ∼ 0 cm -1 ) at various flow conditions at Reynolds numbers in the range of 26 to 3000 showed a good correlation between the different reactor types. In high UV-C absorbing liquids, the inactivation efficiency increases due to the improved radial mixing. The inactivation performance of the Taylor-Couette system correlates to the annular reactor when no rotation force is applied. The residence time distributions showed the narrowest distribution with the coiled tube system at comparable flow rates. The results indicate that, despite the laminar flow conditions, the performance of the Taylor-Couette unit becomes equal to the turbulent flow conditions of the coiled tube reactor by rotation of the inner cylinder.

  2. Low-level bromate analysis in drinking water by ion chromatography with optimized suppressed conductivity cell current followed by a post-column reaction and UV/Vis detection.

    Science.gov (United States)

    Fotsing, Marcellin; Barbeau, Benoit; Prevost, Michele

    2011-01-01

    In the present work, a high capacity anion exchange column was used to efficiently and simultaneously separate traces of oxyhalide disinfection byproducts (DBP) anions and bromide by an ion chromatography system followed by a post-column reaction (PCR). The PCR generates in situ hydroiodic (HI) acid from the excess of potassium iodate that combines with bromate from the column effluent to form the triiodide anion detectable by UV/Vis absorbance at 352 nm. The suppressed conductivity cell current was optimized at 70 mA, with a flow rate of 1.0 mL/min and a 9 mM carbonate eluent. Its performance was investigated on a trace-level determination of bromate in ozonated municipal and bottled drinking water. Based on ozonated municipal drinking water matrix, the method detection limit of 0.27 μg BrO(-)(3)/L was evaluated with the Method Quantification Limit (MQL) of 0.89 μg BrO(-)(3)/L. However, in ultrapure water, a MDL of 0.015 μg BrO(-)(3)/L and a MRL of 0.052 μg BrO(-)(3)/L were achieved. The recovery for spiked municipal samples was in the range of 90%-115%.

  3. Towards high capacity latex-coated porous polymer monoliths as ion-exchange stationary phases.

    Science.gov (United States)

    Hutchinson, Joseph P; Hilder, Emily F; Shellie, Robert A; Smith, Jason A; Haddad, Paul R

    2006-02-01

    The preparation of high capacity agglomerated monolithic ion-exchangers for capillary ion chromatography is described. Post-modification of reactive monoliths was investigated as an alternative to co-polymerisation of a suitable functional monomer with an overarching goal of increasing ion-exchange capacity. Direct sulfonation of poly styrene-co-divinyl benzene monoliths using concentrated sulfuric acid or chlorosulfonic acid was unsuccessful even for monoliths containing as low as 8% crosslinker. In contrast, chemical transformation of reactive monoliths containing glycidyl methacrylate was used to increase the ion-exchange capacity by up to more than thirty-fold with ion exchange capacities of 14-29 microequiv g(-1) achieved. Three different reactions were considered, including reaction with 4-hydroxybenenesulfonic acid under basic conditions; reaction with thiobenzoic acid followed by transformation to a reactive thiol and the subsequent oxidation to the sulfonic acid; and direct sulfonation with sodium sulfite. Of these, the reaction with sodium sulfite resulted in the most significant increase in the capacity and the best separation performance. In the isocratic mode separation efficiencies of over 13,500 plates m(-1) were observed (for iodate). The separation of seven inorganic anions was also demonstrated using a hydroxide gradient.

  4. A study into the consequences of a nuclear accident

    International Nuclear Information System (INIS)

    Arnott, D.G.

    1987-07-01

    The nuclear industry in Britain would like to believe, and would like the general public to believe, that major accidents such as that at Chernobyl in 1986, could no happen in Britain, because the design and operating procedure have been made as safe as possible. However, because the designers and operators are human, they can make mistakes. Some of these are mentioned; errors of design, errors of maintenance or inspection and errors of judgement. In spite of protestations to the contrary, a major accident could occur at Sizewell-B reactor. Given that this a real possibility, plans should be drawn up to prepare for the situation. The study considers the possible consequences of a nuclear accident under the headings, human error, how nuclear fission works, radioactivity, the truth about Chernobyl, what patterns of reactor accident are possible, what can be done (this includes meteorological information, the issuing of potassium iodate tables, radiation monitoring and evacuation). Practical issues which should concern the local authorities, especially Wrekin Council, are discussed and a recommendation made for an environmental protection officer to be appointed to keep the matter under continuing review. (U.K.)

  5. Bone Marrow–Derived Cells Home to and Regenerate Retinal Pigment Epithelium after Injury

    Science.gov (United States)

    Harris, Jeffrey R.; Brown, Gary A. J.; Jorgensen, Marda; Kaushal, Shalesh; Ellis, E. Ann; Grant, Maria B.; Scott, Edward W.

    2013-01-01

    Purpose To determine whether hematopoietic stem and progenitor cells (HSCs/HPCs) can home to and regenerate the retinal pigment epithelium (RPE) after induced injury. Methods Enriched HSCs/HPCs from green fluorescent protein (gfp) transgenic mice were transplanted into irradiated recipient mice to track bone marrow–derived cells. Physical damage was induced by breaching Bruch’s membrane and inducing vascular endothelial growth factor A (VEGFa) expression to promote neovascularization. RPE damage was also induced by sodium iodate injection (40 mg/kg) into wild-type or albino C57Bl/6 mice. Cell morphology, gfp expression, the presence of the Y chromosome, and the presence of melanosomes were used to determine whether the injured RPE was being repaired by the donor bone marrow. Results Injury to the RPE recruits HSC/HPC–derived cells to incorporate into the RPE layer and differentiate into an RPE phenotype. A portion of the HSCs/HPCs adopt RPE morphology, express melanosomes, and integrate into the RPE without cell fusion. Conclusions HSCs/HPCs can migrate to the RPE layer after physical or chemical injury and regenerate a portion of the damaged cell layer. PMID:16639022

  6. Kinetics of iodine removal by washing with water

    International Nuclear Information System (INIS)

    Adachi, Motonari

    1978-01-01

    Removal of iodine vapor by washing with water is an important problem in the safety and protection of environmental air in the surrounding of nuclear facilities. Investigations on its development and practical use have been conducted in Japan. However, it seems to be important that the theoretical proof for these experimental results should be fully made through the fundamental researches. From the above described point of view, absorption mechanism and absorption rate have been investigated concerning iodine removal by washing with water as seen in the previous report. In the investigation, the effect of carbon dioxide on the vapor-liquid equilibrium of iodine in air-sodium hydroxide solution system has been measured by using semi-continuous type and batch type vapor-liquid equilibrium measuring apparatuses. Over-all vapor-liquid partition coefficient of iodine significantly reduced with the increase of carbon dioxide concentration. This is due to the fact that the existence of carbon dioxide greatly decreases the iodine and iodate ions. These experimental results can be explained by considering carbon dioxide reaction in sodium hydroxide solution together with iodine reaction. (Wakatsuki, Y.)

  7. Bi2(IO3)(IO6): First combination of [IO3]- and [IO6]5- anions in three-dimensional framework

    Science.gov (United States)

    Sun, Chuanling; Wu, Yuandong; Mei, Dajiang; Doert, Thomas

    2018-03-01

    A new bismuth (III) iodate periodate, Bi2(IO3)(IO6) was obtained from hydrothermal reactions using Bi(NO3)3·5H2O, and H5IO6 as starting materials. Bi2(IO3)(IO6) crystallizes in the monoclinic space group P21/c (No. 14) with lattice parameters ɑ = 8.1119(6), b = 5.4746(4), c = 16.357(1) Å, β = 99.187(2)°, V = 717.07(9) Å3, Z = 4. The structure of Bi2(IO3)(IO6) features a three-dimensional framework which is a combination of [Bi(1)O5] tetragonal pyramids, [Bi(2)O8] bicapped trigonal prisms and [IO3]- and [IO6]5- anions. Thermal analysis shows that the compound is thermally stable up to about 350 °C. The solid state UV-vis-NIR diffuse reflectance spectrum indicates that Bi2(IO3)(IO6) is a semiconductor with a band gap of 2.76 eV.

  8. [Determination of iodine and its species in plant samples using ion chromatography-inductively coupled plasma mass spectrometry].

    Science.gov (United States)

    Lin, Li; Chen, Guang; Chen, Yuhong

    2011-07-01

    A method was established for the determination of iodine and its species in plant samples using ion chromatography-inductively coupled plasma mass spectrometry (IC-ICP/ MS). Alkaline extraction and IC-ICP/MS were applied as the sample pre-treatment method and the detection technique respectively, for iodate and iodide determination. Moreover, high-temperature pyrolysis absorption was adopted as the pre-treatment method for total iodine analysis, which finally converted all the iodine species into iodide and measured the iodide by IC-ICP/MS. The recoveries of iodine for alkaline extraction and high-temperature pyrolysis absorption were 89.6%-97.5% and 95.2%-111.2%, respectively. The results were satisfactory. The detection limit of iodine was 0.010 mg/kg. The iodine and its speciation contents in several kinds of plant samples such as seaweeds, kelp, cabbage, tea leaf and spinach were investigated. It was shown that the iodine in seaweeds mainly existed as organic iodine; while the ones in kelp, cabbage, tea leaf and spinach mainly existed as inorganic iodine.

  9. A comparison of the predictions of the INSPECT reaction set with experimental data

    International Nuclear Information System (INIS)

    Barton, R.A.; Sims, H.E.

    1992-01-01

    thermal chemistry of iodine over a wide range of conditions of pH and temperature to which the chemistry of iodine is particularly sensitive. These conditions of temperature (30 deg. C - 90 deg. C) and pH (4.6 - 8) are generally those expected for fault conditions. The work gives confidence in the reaction scheme in two ways. First the prediction of the trends of decreasing I 2 production both with increasing pH and and with increasing temperature shows that the reaction set incorporates sufficient reactions to span the conditions of interest and also that no major reaction has been been omitted. Second the good quantitative agreement between prediction and experimental data from our own laboratory and independent data from overseas gives confidence in the use of the model for the quantitative prediction of iodine chemistry not only in laboratory conditions but also in faults. There are two aspects of uncertainty. In particular the reactions of hydrogen peroxide are suspect and it would need an experimental programme to resolve the kinetics and mechanisms. The radiation chemistry of iodate is also uncertain but is probably not so important as iodate is only important at low concentrations where the radiological hazard is reduced. (authors)

  10. CHEMO-hydrodynamic coupling between forced advection in porous media and self-sustained chemical waves

    Science.gov (United States)

    Atis, S.; Saha, S.; Auradou, H.; Martin, J.; Rakotomalala, N.; Talon, L.; Salin, D.

    2012-09-01

    Autocatalytic reaction fronts between two reacting species in the absence of fluid flow, propagate as solitary waves. The coupling between autocatalytic reaction front and forced simple hydrodynamic flows leads to stationary fronts whose velocity and shape depend on the underlying flow field. We address the issue of the chemico-hydrodynamic coupling between forced advection in porous media and self-sustained chemical waves. Towards that purpose, we perform experiments over a wide range of flow velocities with the well characterized iodate arsenious acid and chlorite-tetrathionate autocatalytic reactions in transparent packed beads porous media. The characteristics of these porous media such as their porosity, tortuosity, and hydrodynamics dispersion are determined. In a pack of beads, the characteristic pore size and the velocity field correlation length are of the order of the bead size. In order to address these two length scales separately, we perform lattice Boltzmann numerical simulations in a stochastic porous medium, which takes into account the log-normal permeability distribution and the spatial correlation of the permeability field. In both experiments and numerical simulations, we observe stationary fronts propagating at a constant velocity with an almost constant front width. Experiments without flow in packed bead porous media with different bead sizes show that the front propagation depends on the tortuous nature of diffusion in the pore space. We observe microscopic effects when the pores are of the size of the chemical front width. We address both supportive co-current and adverse flows with respect to the direction of propagation of the chemical reaction. For supportive flows, experiments and simulations allow observation of two flow regimes. For adverse flow, we observe upstream and downstream front motion as well as static front behaviors over a wide range of flow rates. In order to understand better these observed static state fronts, flow

  11. New Ir Bis-Carbonyl Precursor for Water Oxidation Catalysis

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Daria L. [Department of Chemistry, Yale University, 225; Beltrán-Suito, Rodrigo [Department of Chemistry, Yale University, 225; Thomsen, Julianne M. [Department of Chemistry, Yale University, 225; Hashmi, Sara M. [Department of Chemical and Environmental; Materna, Kelly L. [Department of Chemistry, Yale University, 225; Sheehan, Stafford W. [Catalytic Innovations LLC, 70 Crandall; Mercado, Brandon Q. [Department of Chemistry, Yale University, 225; Brudvig, Gary W. [Department of Chemistry, Yale University, 225; Crabtree, Robert H. [Department of Chemistry, Yale University, 225

    2016-02-05

    This paper introduces IrI(CO)2(pyalc) (pyalc = (2-pyridyl)-2-propanoate) as an atom-efficient precursor for Ir-based homogeneous oxidation catalysis. This compound was chosen to simplify analysis of the water oxidation catalyst species formed by the previously reported Cp*IrIII(pyalc)OH water oxidation precatalyst. Here, we present a comparative study on the chemical and catalytic properties of these two precursors. Previous studies show that oxidative activation of Cp*Ir-based precursors with NaIO4 results in formation of a blue IrIV species. This activation is concomitant with the loss of the placeholder Cp* ligand which oxidatively degrades to form acetic acid, iodate, and other obligatory byproducts. The activation process requires substantial amounts of primary oxidant, and the degradation products complicate analysis of the resulting IrIV species. The species formed from oxidation of the Ir(CO)2(pyalc) precursor, on the other hand, lacks these degradation products (the CO ligands are easily lost upon oxidation) which allows for more detailed examination of the resulting Ir(pyalc) active species both catalytically and spectroscopically, although complete structural analysis is still elusive. Once Ir(CO)2(pyalc) is activated, the system requires acetic acid or acetate to prevent the formation of nanoparticles. Investigation of the activated bis-carbonyl complex also suggests several Ir(pyalc) isomers may exist in solution. By 1H NMR, activated Ir(CO)2(pyalc) has fewer isomers than activated Cp*Ir complexes, allowing for advanced characterization. Future research in this direction is expected to contribute to a better structural understanding of the active species. A diol crystallization agent was needed for the structure determination of 3.

  12. The MacDonald and savage titrimetric procedure for plutonium scaled-down to the milligram level: Automated procedure for routine analysis of safeguards samples containing 2 to 5 mg plutonium

    International Nuclear Information System (INIS)

    Ronesch, K.; Jammet, G.; Berger, J.; Doubek, N.; Bagliano, G.; Deron, S.

    1992-08-01

    A selective titrimetric procedure directly applicable to both input and product solutions from fast reactor fuel reprocessing was set up by MacDonald and Savage and scaled down to 3 mg of plutonium in sample aliquots at the request of the Safeguards Analytical Laboratory (SAL) of the International Atomic Energy Agency (IAEA), which needed to replace its silver (II) oxide titration procedure by a more selective electrochemical method. Although the procedure is very selective the following species still interfere: Vanadates (almost quantitatively), Neptunium (one electron exchange per mole); Nitrites, Fluorosilicates and Iodates present in mg amount yield slight biases. This paper describes the fully automatized procedure presently applied in SAL for the routine determination of 2 to 5 mg plutonium dissolved in nitric acid solution. The method allows the unattended analysis of 20 aliquots within a five hour period. The equipment including the reagent distribution system, the sample changer and the control units are introduced and the principle design of the software is shortly described. Safety requirements have been addressed and are also reviewed in the report. Results obtained on standard reference materials, international intercomparison samples and actual safeguards samples routinely analyzed with the proposed procedure are presented and compared with results achieved with the semiautomatic mode to demonstrate the performance. International requirements to reduce the amount of radioactive materials in waste will certainly lead to a further reduction of the amount of plutonium in one aliquot. Some future perspective to titrate 1 mg samples are presented in the discussion. 12 refs, 10 figs, 8 tabs

  13. Visible light water oxidation using a co-catalyst loaded anatase-structured Ti(1-(5x/4))Nb(x)O(2-y-δ)N(y) compound.

    Science.gov (United States)

    Breault, Tanya M; Brancho, James J; Guo, Ping; Bartlett, Bart M

    2013-08-19

    The photocatalytic activity of anatase-structured Ti(1-(5x/4))Nb(x)O(2-y-δ)N(y) (x = 0.25, y = 0.02; NbN-25) was examined for water oxidation under UV and visible light irradiation. The semiconductor was prepared by sol-gel processing followed by nitridation in flowing ammonia and exhibits an indirect optical gap of 2.2 eV. Ti(1-(5x/4))Nb(x)O(2-y-δ)N(y) was loaded with RuO2 by an impregnation technique, and optimized conditions reveal that 1 wt % RuO2 generates 16 μmol O2 from water with concomitant IO3(-) reduction after 3 h of illumination under simulated solar radiation at a flux of 600 mW/cm(2) illumination, which corresponds to 6-sun AM1.5G illumination (compared to no detectible O2 without the RuO2 cocatalyst). A series of cut-on filters shows that the catalyst-loaded semiconductor evolves O2 for λ ≤ 515 nm, and a gas-phase mass spectrometry isotope labeling experiment shows that irradiating an iodate solution in H2(18)O in the presence of 1 wt % RuO2 loaded on NbN-25 gives rise to catalytic water oxidation: both (36)O2 and (34)O2 are observed. It is unclear whether (16)O arises from IO3(-) or surface reconstruction on the photocatalyst, but ICP-AES analysis of the postirradiated solution shows no dissolved metal ions.

  14. PVC Based Membrane of Ti(IV Iodovanadate for Pb(II Determination

    Directory of Open Access Journals (Sweden)

    Mu. Naushad

    2008-08-01

    Full Text Available Ti(IV iodovanadate has been synthesized by mixing a mixture of aqueous solutions of 0.1 M sodium vanadate and 0.1 M potassium iodate with 0.1 M solution of Ti(IV chloride at pH 1.0. Distribution coefficients (Kd of various metal ions were determined on the column of Ti(IV iodovanadate which showed the selectivity of Pb(II ions by this cation exchange material. So Ti(IV iodovanadate has been used as an electoactive material for the construction of Pb(II selective electrode. The main purpose of this study is to develop an inexpensive, simple and reliable ion-selective electrode for Pb(II determination. The sensor exhibit Nernstian response for Pb(II ions over a wide concentration range of 1 x 10-7 M to 1 x 10-1 M with a slope of 30±0.4 mV per decade of activity. The electrode is suitable for use in aqueous solution in a pH range of 2-7.2 with a response time of 10 second. The membrane electrode can be used at least for 4 months without any divergence in potential. The selectivity coefficients were determined by the mixed solution method and revealed that the electrode was selective for Pb(II ions in the presence of interfering cations. The sensor could be used as an indicator electrode in the potentiometric titration of Pb(II ions with EDTA. The practical applicability of the proposed sensor has been reported for Pb(II determination in a standard rock sample and water sample. The results are found to be in good agreement with those obtained by using conventional methods.

  15. A study on the expulsion of iodine from spent-fuel solutions

    Energy Technology Data Exchange (ETDEWEB)

    Sakurai, Tsutomu; Takahashi, Akira; Ishikawa, Niroh [Japan Atomic Energy Research Institute, Ibaraki-ken (Japan)] [and others

    1995-02-01

    During dissolution of spent nuclear fuels, some radioiodine remains in spent-fuel solutions. Its expulsion to dissolver off-gas is important to minimize iodine escape to the environment. In our current work, the iodine remaining in spent-fuel solutions varied from 0 to 10% after dissolution of spent PWR-fuel specimens (approximately 3 g each). The amount remaining probably was dependent upon the dissolution time required. The cause is ascribable to the increased nitrous acid concentration that results from NOx generated during dissolution. The presence of nitrous acid was confirmed spectrophotometrically in an NO-HNO{sub 3} system at 100{degrees}C. Experiments examining NOx concentration versus the quantity of iodine in a simulated spent-fuel solution indicate that iodine (I{minus}) in spent fuels is subjected to the following three reactions: (1) oxidation into I{sub 2} by nitric acid, (2) oxidation into I{sub 2} by nitrous acid arising from NOx, and (3) formation of colloidal iodine (AgI, PdI{sub 2}), the major iodine species in a spent-fuel solution. Reaction (2) competes with reaction (3) to control the quantity of iodine remaining in solution. The following two-step expulsion process to remove iodine from a spent-fuel solution was derived from these experiments: Step One - Heat spent-fuel solutions without NOx sparging. When aged colloidal iodine is present, an excess amount of iodate should be added to the solution. Step Two - Sparge the fuel solution with NOx while heating. Effect of this new method was confirmed by use of a spent PWR-fuel solution.

  16. Association of iodine status with IQ level and academic achievement of rural primary school children in West Bengal, India

    Directory of Open Access Journals (Sweden)

    Koushik Bhowal

    2014-12-01

    Full Text Available Background: Iodine being an integral component of the thyroid hormones is crucial for physical and mental development. Iodine status & intake is often measured by a surrogate measure, namely urine iodine excretion, as almost all ingested iodine is excreted in the urine. Aims &Objectives: To investigate the body Iodine status of rural primary school children and its association with their intelligence level (IQ & academic achievement. Materials & Methods: A cross-sectional analytical study was carried out in three Government schools in the district of 24 Parganas, West Bengal, India among  300 children (150 boys & 150 girls aged 6 to 8 years  studying in class II to IV. Urinary iodine was estimated by the 'Wet Digestion Method (Sandell-Kolthoff reaction. IQ level was evaluated using Ravens Progressive Matrices test. Academic achievement was evaluated on the marks obtained in the term end examinations.  Result: 12.34%, 15.6% & 24.3% of the children were in the severe, moderate & mild range of iodine deficiency in terms of urinary iodine excretion. It was found that 85.67% & 14.33% of the children were consumed iodated salt ≥15 ppm &< 15 ppm of iodine level. 0.67%, 5% & 27.34 % of them achieved A, B & C of IQ grades, respectively.62.34 % of the students achieved first three academic grades. Body Iodine status of the children has significant positive correlation (P<0.01 with IQ grades and academic achievement. Academic achievement of the children has significant positive correlation (P<0.05 with their intelligence level. Conclusions: Poor body Iodine status of the rural primary school children may be one of the causes for their poor intelligence level and academic achievement.

  17. Marine redox structure at the culmination of the Great Oxidation Event: Insights from the Zaonega Formation, Karelia, Russia

    Science.gov (United States)

    Kipp, M.; Lepland, A.; Buick, R.

    2017-12-01

    The availability of dissolved oxygen is thought to have been the dominant throttle on the evolution and diversification of eukaryotic life during the Proterozoic Eon [1]. In the mid-Proterozoic, during the interval that presaged the rise of eukaryotes to ecological dominance, oxygen scarcity is thought to have relegated eukaryotic organisms to slivers of oxygenated shallow oceans [2]. However, recent work has suggested that oxygen levels rose dramatically during the early Paleoproterozoic Great Oxidation Event before crashing to the low levels of the mid-Proterozoic [3]. Evidence from selenium isotopes in shales [4] and iodate concentrations in carbonates [5] has even suggested that wide swathes of continental shelves were oxic enough to support eukaryotic organisms at this time. How oxic though, and for how long, remain poorly constrained. Here we present new selenium geochemical data from the Zaonega Formation of Karelia, Russia that can help resolve those questions. Previous work has proposed that the Zaonega Formation, and correlative Francevillian Series of Gabon, record the establishment of an oxygen-rich atmosphere at the culmination of the GOE [6]. Our selenium isotope dataset provides a test for this hypothesis, and can also be used to assess the preservation of the geochemical signatures in the Zaonega Formation. These data point to regional redox fluctuations, but due to the short marine residence time of selenium, extrapolating these results to global phenomena remains difficult. 1. Reinhard, et al (2016) PNAS 2. Planavsky, et al (2014) Science 3. Bekker and Holland (2012) EPSL 4. Kipp, et al (2017) PNAS 5. Hardisty, et al (2014) Geology 6. Kump, et al (2011) Science

  18. Place and achieving a magistral preparation in a service of nuclear medicine: example of the IBZM; Place et realisation d`une preparation magistrale dans un service de medecine nucleaire: exemple de l`IBZM

    Energy Technology Data Exchange (ETDEWEB)

    Zimmer, L.; Baulieu, J.L.; Bugeon, S.; Besnard, J.C.; Guilloteau, D. [CHU Tours (France)

    1997-12-31

    The radio-pharmacist is competent and a legal licensee to realizing magistral preparations, defined in the book V of public health Code. We present here the case of a radiopharmaceutical drug prepared extemporary on a medical prescription, the labelling of BZM by iodine 123. The choice of this molecule is made after obtaining the indispensable pre-requisites (lack of noxiousness, teratogenicity, validation by pre-clinic studies, etc). The IBZM allows achieving the etiologic diagnosis of extra-pyramidal syndromes by scintigraphic visualisation of central D2 dopaminergic receptors. The magistral preparation of a radiopharmaceutical implies: (1). Identification of the row materials indispensable in warranting the labelling quality and innocuity of the final injected product. This is done by means of routine chemical reactions, described by France Pharmacopoeia or specifically established. Thus, all the row materials are tested and referenced prior to utilization. (2). The radio-labelling is effected in the day of the examination following a validated procedure: labelling of BZM by sodium iodate in buffer acid medium, extraction of formed IBZM by an organic solvent, purification of IBZM by HPCL, brought in injectable form by chromatographic passage (Sep Pack) and sterilizing filtration. (3). The test of final product is done prior to its injection by measuring the pH and co-elution by HPLC with the cool standard product. The IBZM is delivered providing its radiochemical purity is higher than 90%. A sterility test of preparation is effected a posteriori. The magistral preparation of IBZM allows neurological scintigraphic examinations, still unique in nuclear medicine. Other radiopharmaceuticals with cerebral use will be proposed to clinicians by radio-pharmacists. In all the these cases, the quality of injected labeller will be warranted by the same pharmaceutic approach

  19. Production of gaseous radiotracers CH3I and I2 through Na123I salt

    International Nuclear Information System (INIS)

    Candeiro, R.E.M.; Pereira, W.P.

    2011-01-01

    The objective of the present work was to develop, separately, methodology for production of two gaseous tracers through the sodium iodide NaI marked with 123 I. Found in the nature in form different, the iodine has been used in diverse works in the area of the industry and health. These two forms of the gaseous iodine, the methyl iodide, CH 3 I, and molecular iodine, I 2 , are very unstable and volatile in the ambient temperature and presents different problems in clean-up and monitoring systems. The syntheses were processed with sodium iodide (NaI) 1M aqueous solution marked with 1 23I . The production of gas I 2 was realized with in chlorine acid (HCl) and sodium iodate salt (NaIO 3 ) and the CH 3 I was used, the salt of NaI and the reagent (CH 3 ) 2 SO 4 . The production of gases was initially realized through in unit in glass with an inert material and the purpose was to study the kinetic of reaction and to determine the efficiency of production. The two synthesis occurs in the reaction bottle and after of produced, the gas is stored in the collect bottle that contains a starch solution for fixed the I 2 , and in syntheses of CH 3 I contains a silver nitrate solution for your fixation. To determine the efficiency of production of gases, analytic tests were realized, where the consumption of iodide ions of the bottle of reaction are measured. The optimization of production of the each gaseous tracer was studied varying parameter as: concentration of iodide, concentration of acid and temperature. After, the syntheses of the radiotracers were realized in the compact unit, having been used as main reagent the salt radiated of sodium iodide, Na 123 I. The transportation of elementary iodine and methyl iodine was studied by a scintillation detector NaI (2 x 2)' positioned in the reaction bottle. (author)

  20. Consumption of a Double-Fortified Salt Affects Perceptual, Attentional, and Mnemonic Functioning in Women in a Randomized Controlled Trial in India.

    Science.gov (United States)

    Wenger, Michael J; Murray-Kolb, Laura E; Nevins, Julie Eh; Venkatramanan, Sudha; Reinhart, Gregory A; Wesley, Annie; Haas, Jere D

    2017-12-01

    Background: Iron deficiency and iron deficiency anemia have been shown to have negative effects on aspects of perception, attention, and memory. Objective: The purpose of this investigation was to assess the extent to which increases in dietary iron consumption are related to improvements in behavioral measures of perceptual, attentional, and mnemonic function. Methods: Women were selected from a randomized, double-blind, controlled food-fortification trial involving ad libitum consumption of either a double-fortified salt (DFS) containing 47 mg potassium iodate/kg and 3.3 mg microencapsulated ferrous fumarate/g (1.1 mg elemental Fe/g) or a control iodized salt. Participants' blood iron status (primary outcomes) and cognitive functioning (secondary outcomes) were assessed at baseline and after 10 mo at endline. The study was performed on a tea plantation in the Darjeeling district of India. Participants ( n = 126; 66% iron deficient and 49% anemic at baseline) were otherwise healthy women of reproductive age, 18-55 y. Results: Significant improvements were documented for iron status and for perceptual, attentional, and mnemonic function in the DFS group (percentage of variance accounted for: 16.5%) compared with the control group. In addition, the amount of change in perceptual and cognitive performance was significantly ( P < 0.05) related to the amount of change in blood iron markers (mean percentage of variance accounted for: 16.0%) and baseline concentrations of blood iron markers (mean percentage of variance accounted for: 25.0%). Overall, there was evidence that the strongest effects of change in iron status were obtained for perceptual and low-level attentional function. Conclusion: DFS produced measurable and significant improvements in the perceptual, attentional, and mnemonic performance of Indian female tea pickers of reproductive age. This trial was registered at clinicaltrials.gov as NCT01032005. © 2017 American Society for Nutrition.

  1. Determination of chemical form of iodine with IC-ICP-MS system and its application to the environmental samples

    International Nuclear Information System (INIS)

    Yoshida, S.; Katou, S.; Sekimoto, H.; Muramatsu, Y.

    2005-01-01

    Iodine-129 is one of the important radionuclides possibly released into the environment from nuclear weapons testing and from the nuclear facilities such as nuclear fuel reprocessing plants. Because of its long half-life (1.57 x 10 7 y), knowing its long-term behavior in the environment is a major concern. As I-129 is expected to act together with stable iodine (I-127) in the environment after long time, the biogeochemical cycling of stable iodine in the environment can be used for the reliable safety assessment of I-129. Chemical form is the one of the important factors controlling the 'iodine behavior in the environment. Iodide (I - ) and iodate (IO 3 - ) are known to be the major chemical form in the aqueous solution. However, the information on the chemical form of iodine in the environmental sample is limited because of lack of reliable analytical technique for trace level of iodine in the environment. In this study, the analytical system by using ion chromatograph (IC) followed by inductively coupled plasma mass spectrometry (ICP-MS) was developed for the separate determination of I - and IO 3 - in the aqueous solution. The IC with anion exchange column (EXCELPAK ICS-A23) was used for the separation of I - and IO 3 - with 30 mM (NH 4 ) 2 CO 3 as eluent. Separated iodine was determined with ICP-MS on line. with the detection limit 0.1 - 1 μg/L. The total iodine concentration was also measured by the direct determination with ICP-MS. The iodine in the several environmental samples such as irrigation water in paddy field was successfully determined with information of chemical form. In incubation experiment with flooded soil, the change of the chemical form of iodine in the soil solution with change of Eh was observed. Detailed data will be discussed in the presentation.

  2. I-131 Extraction from Fresh water and Sewage plant effluent

    Energy Technology Data Exchange (ETDEWEB)

    Souti, Maria-Evangelia; Hormann, Volker; Toma, Edda; Fischer, Helmut W. [University of Bremen, Institute of Environmental Physics, Otto-Hahn-Alle 1, D-28359 Bremen (Germany)

    2014-07-01

    The amount of maximum I-131 body activity of a patient released from a hospital in Germany (250 MBq) is comparable to the yearly reported total release of I-131 from all commercial nuclear power plants to ambient air and water. A large fraction of the body activity will be excreted and find its way to surface waters, through the sewage system. Thus medical iodine is the major contributor to the environmental I-131 in surface waters. Due to the path it follows (patient-sewage-sewage plant-fresh water) it can form organic complexes and as a result its concentration of organic iodine is relatively high. Existing methods, focusing on the removal of mainly iodide (I{sup -}) and iodate (IO{sub 3}{sup -}), were found to be insufficient to successfully extract the iodine from environmental samples, leading to highly variable results depending on the contribution of organic iodine. The reported work is based on testing and modifying existing methods. In order to accomplish the highest iodine yield, the inorganic iodine extraction is followed by a supplementary procedure for additionally separating the iodine bound to dissolved organic matter. The results show only slight variations of the I-131 extraction yield which is close to 90%, constituting this method as appropriate for successfully extracting I-131 from environmental samples (WWTP effluent, river water, lake water). Another advantage of our method is its applicability to high volume samples (20 L, 50 L), making it possible for a gamma spectrometer to detect activities as low as 0.5 mBq/l. (authors)

  3. Development, validation, and application of a novel LC-MS/MS trace analysis method for the simultaneous quantification of seven iodinated X-ray contrast media and three artificial sweeteners in surface, ground, and drinking water.

    Science.gov (United States)

    Ens, Waldemar; Senner, Frank; Gygax, Benjamin; Schlotterbeck, Götz

    2014-05-01

    A new method for the simultaneous determination of iodated X-ray contrast media (ICM) and artificial sweeteners (AS) by liquid chromatography-tandem mass spectrometry (LC-MS/MS) operated in positive and negative ionization switching mode was developed. The method was validated for surface, ground, and drinking water samples. In order to gain higher sensitivities, a 10-fold sample enrichment step using a Genevac EZ-2 plus centrifugal vacuum evaporator that provided excellent recoveries (90 ± 6 %) was selected for sample preparation. Limits of quantification below 10 ng/L were obtained for all compounds. Furthermore, sample preparation recoveries and matrix effects were investigated thoroughly for all matrix types. Considerable matrix effects were observed in surface water and could be compensated by the use of four stable isotope-labeled internal standards. Due to their persistence, fractions of diatrizoic acid, iopamidol, and acesulfame could pass the whole drinking water production process and were observed also in drinking water. To monitor the fate and occurrence of these compounds, the validated method was applied to samples from different stages of the drinking water production process of the Industrial Works of Basel (IWB). Diatrizoic acid was found as the most persistent compound which was eliminated by just 40 % during the whole drinking water treatment process, followed by iopamidol (80 % elimination) and acesulfame (85 % elimination). All other compounds were completely restrained and/or degraded by the soil and thus were not detected in groundwater. Additionally, a direct injection method without sample preparation achieving 3-20 ng/L limits of quantification was compared to the developed method.

  4. Validation of 123I-6-deoxy-6-iodo-D-glucose (6-DIC) as tracer for the in-vivo glucose transport

    International Nuclear Information System (INIS)

    Perret, P.; Ghezzi, C.; Mathieu, J.P.; Morin, C.; Vidal, M.; Comet, M.; Fagret, D.

    1997-01-01

    The evaluation of the glucose transport is very important clinically because alterations of this transport were described in numerous pathologies, in neurology, oncology and endocrinology. A new analog of the 123 I-labelled has been synthesized: 123 I-6-deoxy-6-iodo-D-glucose (6-DIG). Its in-vitro biological behaviour is similar to that of 3-O-methyl-D-glucose (3-OMG), the reference tracer of glucose transport. The aim of the study was to determine if it is possible to make evident by 6-DIG a variations of in-vivo glucose transport. The studies were effected on a model of homozygote mice (db/db), genetically diabetic (NIDDM), presenting a severe insulin-resistance, characterized by deficient glucose transport in response to insulin. The studies of 6-DIG biodistribution (5 nmol/mouse) with (1.5 UI/Kg) or without exogenous insulin, were conducted in diabetic mice (db/db) and in non-diabetic (db/+) control mice. The results show that the capture of 6-DIG, as well as that of glucose, increases (by 30%) in response to insulin in most of insulin-sensitive tissues in control mice. In the insulin-resistant and hyperglycemic db/db mouse, the capture of 6-DIG is not modified, no matter whether the exogenous insulin is present. In conclusion, the 6-DIG is able to make evident a lack of glucose transport in heart, diaphragm and skeletal muscle in diabetic mouse and a physiological variation of this transport in response to insulin, in the control mouse. This result should be stressed because for the first time it is possible to evidence in-vivo variations into glucose transport with a iodated molecule

  5. Spectrophotometric and potentiometric determination of piroxicam and tenoxicam in pharmaceutical preparations.

    Science.gov (United States)

    El-Ries, Mohamed A; Mohamed, Gehad; Khalil, Shaeban; El-Shall, Manal

    2003-01-01

    Two simple and accurate methods are described for the determination of piroxicam and tenoxicam in their pharmaceutical preparations. The spectrophotometric method involves the oxidation of these drugs with potassium iodate in acid medium with the liberation of iodine and subsequent extraction with cyclohexane followed by measuring the absorbance at lambda=522 nm. Beer's law is obeyed in the concentration range of 0.05-1.1 and 0.05-0.6 mg x ml(-1) for piroxicam and tenoxicam, respectively. The apparent molar absorptivities of the resulting coloured products are found to be 2.7 x 10(3) and 2.5 x 10(3) l mol(-1) x cm(-1), whereas Sandell sensitivities are 0.012 and 0.013 g x cm(-2) for piroxicam and tenoxicam, respectively. The potentiometric method involves the direct titration of both drugs with N-bromosuccinimide in acid medium and the end point is determined potentiometrically using platinum indicator electrode. Piroxicam and tenoxicam can be determined quantitatively in the concentration range of 0.33-3.37 and 0.33-4.08 mg x ml(-1) for tenoxicam and piroxicam, respectively. The standard deviation and relative standard deviation values are found to be ranged from 0.05-0.07 and 0.37-0.98% and 0.025-0.078 and 0.25-1.2% for tenoxicam and piroxicam, respectively. The two methods are accurate within +/-1.0%. Optimum conditions affecting both methods are studied. The proposed methods are applied for the determination of the drugs in pure form and in commercial pharmaceutical preparations.

  6. Halogen species record Antarctic sea ice extent over glacial–interglacial periods

    Directory of Open Access Journals (Sweden)

    A. Spolaor

    2013-07-01

    Full Text Available Sea ice is an integral part of the earth's climate system because it affects planetary albedo, sea-surface salinity, and the atmosphere–ocean exchange of reactive gases and aerosols. Bromine and iodine chemistry is active at polar sea ice margins with the occurrence of bromine explosions and the biological production of organoiodine from sea ice algae. Satellite measurements demonstrate that concentrations of bromine oxide (BrO and iodine oxide (IO decrease over sea ice toward the Antarctic interior. Here we present speciation measurements of bromine and iodine in the TALDICE (TALos Dome Ice CorE ice core (159°11' E, 72°49' S; 2315 m a.s.l. spanning the last 215 ky. The Talos Dome ice core is located 250 km inland and is sensitive to marine air masses intruding onto the Antarctic Plateau. Talos Dome bromide (Br− is positively correlated with temperature and negatively correlated with sodium (Na. Based on the Br−/Na seawater ratio, bromide is depleted in the ice during glacial periods and enriched during interglacial periods. Total iodine, consisting of iodide (I− and iodate (IO3−, peaks during glacials with lower values during interglacial periods. Although IO3− is considered the most stable iodine species in the atmosphere it was only observed in the TALDICE record during glacial maxima. Sea ice dynamics are arguably the primary driver of halogen fluxes over glacial–interglacial timescales, by altering the distance between the sea ice edge and the Antarctic plateau and by altering the surface area of sea ice available to algal colonization. Based on our results we propose the use of both halogens for examining Antarctic variability of past sea ice extent.

  7. Experiments on The Retention of The Fission Product Iodine in Nuclear Reactor Accidents

    Energy Technology Data Exchange (ETDEWEB)

    Bruchertseifer, H.; Cripps, R.; Guentay, S.; Jaeckel, B

    2004-03-01

    The paper reports PSI participation in the ICHEMM Project (Iodine Chemistry and Mitigation Mechanisms) of the EU 5th Framework Programme, which has the objective of identifying new possible mitigation processes, or accident management measures, favouring the conversion of volatile iodine species, especially organic iodine released during a severe accident at a Nuclear Power Plant (NPP), into nonvolatile forms. Significant effort has been expended, firstly to develop analytical methods for determining concentrations of the common iodine species (iodide, iodate, molecular iodine and methyl iodide), and secondly to provide missing and important information on decomposition phenomena and involved reactions. Experiments have been conducted at PSI to obtain data on thermal (hydrolysis) and radiolytic decomposition of CH{sub 3}I in aqueous solution under conditions as close as possible to those in an anticipated accident. Radioactive-labelled methyl iodide was used to monitor and quantify the decomposition and to determine the overall mass balance. Results have shown that CH{sub 3}I hydrolysis at 90{sup o}C will dominate over radiolysis at the dose rates (max. 0.4 Gy.s{sup -1}) employed in the experiments. Much increased decomposition rates of CH{sub 3}I have been achieved with chemical reagents (additives), such as sodium thiosulphate or ammonium sulphide. After completion of the ICHEMM Project, further advances have been made from experiments carried out on additives (especially in combination with Aliquat 336) in terms of a fast and complete retention of iodine. The data from these experiments are of direct relevance to severe accident management for both PWR and BWR systems. The impact of the results on possible strategies for management of radioactive waste has also been investigated. (author)

  8. Simulation for separation of radioisotopes I-123 from tellurium target using tracer I-131

    International Nuclear Information System (INIS)

    Sarwono, Daya Agung; Amiruddin, Cahyana; Abidin; Lubis, Hotman

    2013-01-01

    Radioisotope Iodine-123 ( 123 I) can be used as material for the preparation of radiopharmaceutical imaging with SPECT tool. This is caused to 123 I emits gamma rays with energies 159 keV and a half-life 13.2 h. 123 I radioisotope was made from the target material in the form of a thin layer of solid tellurium targets with the reaction 123 Te (p, n) 123 I in energy protons 8-15 MeV or 124 Te (p, 2n) 123 I in the 20-26 MeV proton energy using the cyclotron. The use of I-131 tracer to simulate the separation of I-123 radioisotope from the tellurium target because BATAN Cyclotron CS-30 have not produce current yet so it can not generate a radioisotope I-123. Simulation of I-123 radioisotope separation from the tellurium target using tracer I-131 can be performed by irradiating solid tellurium targets in the reactor. Separation is conducted by dissolving Te targets in the target puck into the dissolution vessel with CrO 3 and H 2 SO 4 then insert to the distillation flask. Furthermore, tellurium irradiated in the reactor as a tracer was added to the distillation flask to be dissolved along with tellurium the results of electroplating. Before distilled done first iodate is reduced with oxalic acid to produce iodine. Iodine was formed, then carried distillation and distillate containing I accommodated with an alkaline solution containing sulfite Based on the results of separation experiments three times the yield were obtained with respectively 12.85%, 13.9% and 5.2% with 1-131 radio nuclide purity of 100%. (author)

  9. Technetium, Iodine, and Chromium Adsorption/Desorption Kd Values for Vadose Zone Pore Water, ILAW Glass, and Cast Stone Leachates Contacting an IDF Sand Sequence

    Energy Technology Data Exchange (ETDEWEB)

    Last, George V. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Snyder, Michelle M.V. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Um, Wooyong [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Stephenson, John R. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Leavy, Ian I. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Strickland, Christopher E. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Bacon, Diana H. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Qafoku, Nikolla [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Serne, R. Jeffrey [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

    2015-11-01

    Performance and risk assessments of immobilized low-activity waste (ILAW) at the Integrated Disposal Facility (IDF) have shown that risks to groundwater are quite sensitive to adsorption-desorption interactions occurring in the near- and far-field environment. These interactions between the underlying sediments and the contaminants present in the leachates that descend from the buried glass, secondary waste grouts, and potentially Cast Stone low-activity waste packages have been represented in these assessments using the contaminant distribution coefficient (Kd) construct. Some contaminants (99Tc, 129I, and Cr) present in significant quantities in these wastes have low Kd values and tend to drive risk to public health and the environment. Relatively small changes in the Kd value can cause relatively large changes in the retardation factor. Thus, even relatively small uncertainty in the Kd value can result in a relatively large uncertainty in the risk determined through performance assessment modeling. The purpose of this study is to further reduce the uncertainty in Kd values for 99Tc, iodine (iodide and iodate), and Cr (chromate; CrO42-) by conducting systematic adsorption-desorption experiments using actual sand-dominated Hanford formation sediments from beneath the IDF and solutions that closely mimic Hanford vadose zone pore water and leachates from Cast Stone and ILAW glass waste forms. Twenty-four batch and 21 flow-through column experiments were conducted, yielding 261 Kd measurements for these key contaminants, and contributing to our understanding for predicting transport from wastes disposed to the IDF. While the batch Kd methodology is not well-suited for measuring Kd values for non-sorbing species (as noted by the U.S. Environmental Protection Agency), the batch Kd results presented here are not wholly inconsistent with the column Kd results, and could be used for sensitivity purposes. Results from the column experiments are consistent with the best

  10. Adsorption of Chromium from Aqueous Solution Using Polyaniline

    Directory of Open Access Journals (Sweden)

    Majid Riahi Samani

    2011-10-01

    Full Text Available New group of polymers have been synthesized that are conductive of electricity so they are called conducting polymers. One of the most conducting polymers is "polyaniline". In the present study, polyaniline was synthesized by oxidizing aniline monomer under strongly acidic conditions using potassium iodate as an initiator of oxidative polymerization. Synthesized polyaniline as a powder used as an adsorbent to remove chromium from aqueous solution. Experiments were conducted in batch mode with variables such as amount of polyaniline, chromium solution pH and adsorbtion isotherms. Due to presence of Cr (III in solution after using polyaniline, removal mechanism is the combination of surface adsorption and reduction. It seems that polyaniline reduces the Cr(VI to Cr(III and adsorbs the Cr(III and a part of remaining  Cr(VI. It is well known that nitrogen atom in compounds of amine derivative makes co-ordinate bond with positive charge of metals due to the presence of electron in sp3 orbital of nitrogen. The majority of total chromium removal  occurred at 30minute for polyaniline  and the optimum  time for  hexavalent chromium  removal was about 5 min. Polyaniline has the maximum total cheomiume removal at pH, 3-9. The maximum hexavalent chromium removal occurred at acidic pH for polyanilines. The equilibrium adsorption data for polyaniline fitted both Freundlich’s and Langmuir’s isotherms. This research shows that polyaniline can be used as an adsorbent  for removal chromium from aqueous solution.

  11. Status and strategy of the U.S. commercial waste management program. Consolidated Fuel Reprocessing Program

    International Nuclear Information System (INIS)

    Croff, A.G.; Jubin, R.T.

    1983-01-01

    Management of airborne waste generally involves the following steps: recovery, treatment, interim storage, transportation, and disposal. The recovery (retention) of airborne radionuclides is generally well developed since the first-generation processes have been used for iodine and particulates for decades by the DOE nuclear materials production plants. Later-generation processes have been carried separately through the cold pilot-plant stage. However, the design and demonstration of a hot, integrated flowsheet for the recovery of all airborne species to the extent necessary to meet applicable regulations are still required. Treatment of the recovered airborne wastes is generally less-well developed. Tentatively preferred processes have been identified: iodine-barium iodate and/or silver zeolites in concrete with additives; krypton-implanted as ions in a metal alloy and encapsulated in concrete; carbon-barium carbonate in concrete with additives; particulates-encapsulation of HEPA filters in concrete; ruthenium-ruthenium traps encapsulated in concrete. The technology for interim storage and transportation appears to be straightforward engineering extensions of existing technology, assuming that the waste forms listed above are to be employed. Waste disposal concepts are the least well-developed aspect of airborne waste mangement technology. It appears that the long-lived materials such as 129 I, 14 C, and particulates will have to be emplaced in a geologic repository and that shorter-lived airborne waste may be acceptable in shallow-land burial grounds. The long-range goal of the program is to determine all of the steps necessary to manage airborne wastes

  12. Bloodstream-To-Eye Infections Are Facilitated by Outer Blood-Retinal Barrier Dysfunction.

    Directory of Open Access Journals (Sweden)

    Phillip S Coburn

    Full Text Available The blood-retinal barrier (BRB functions to maintain the immune privilege of the eye, which is necessary for normal vision. The outer BRB is formed by tightly-associated retinal pigment epithelial (RPE cells which limit transport within the retinal environment, maintaining retinal function and viability. Retinal microvascular complications and RPE dysfunction resulting from diabetes and diabetic retinopathy cause permeability changes in the BRB that compromise barrier function. Diabetes is the major predisposing condition underlying endogenous bacterial endophthalmitis (EBE, a blinding intraocular infection resulting from bacterial invasion of the eye from the bloodstream. However, significant numbers of EBE cases occur in non-diabetics. In this work, we hypothesized that dysfunction of the outer BRB may be associated with EBE development. To disrupt the RPE component of the outer BRB in vivo, sodium iodate (NaIO3 was administered to C57BL/6J mice. NaIO3-treated and untreated mice were intravenously injected with 108 colony forming units (cfu of Staphylococcus aureus or Klebsiella pneumoniae. At 4 and 6 days postinfection, EBE was observed in NaIO3-treated mice after infection with K. pneumoniae and S. aureus, although the incidence was higher following S. aureus infection. Invasion of the eye was observed in control mice following S. aureus infection, but not in control mice following K. pneumoniae infection. Immunohistochemistry and FITC-dextran conjugate transmigration assays of human RPE barriers after infection with an exoprotein-deficient agr/sar mutant of S. aureus suggested that S. aureus exoproteins may be required for the loss of the tight junction protein, ZO-1, and for permeability of this in vitro barrier. Our results support the clinical findings that for both pathogens, complications which result in BRB permeability increase the likelihood of bacterial transmigration from the bloodstream into the eye. For S. aureus, however, BRB

  13. Online coupling of fully automatic in-syringe dispersive liquid-liquid microextraction with oxidative back-extraction to inductively coupled plasma spectrometry for sample clean-up in elemental analysis: A proof of concept.

    Science.gov (United States)

    Horstkotte, Burkhard; Fikarová, Kateřina; Cocovi-Solberg, David J; Sklenářová, Hana; Solich, Petr; Miró, Manuel

    2017-10-01

    A proof of concept of a novel automatic sample cleanup approach for metal assays in troublesome matrixes as a front-end sample pre-treatment to inductively coupled plasma optical emission spectroscopy - ICP-OES - is herein presented. Target metals, namely, copper, lead, and cadmium were complexed in-system quantitatively using ammonium pyrrolidine dithiocarbamate (APDC) and transferred into a minute volume of toluene as extractant employing lab-in-syringe magnetic stirring-assisted dispersive liquid-liquid microextraction (LIS-MSA-DLLME). After discharge of the sample, the analytes were back-extracted into nitric acid and injected on-line into ICP-OES. To promote and expedite this process in-syringe, advantage was taken from oxidative decomposition of the chelate by potassium iodate, reported in this article for the first time. Experimental conditions for LIS-MSA-DLLME were optimized by Box-Benkhen multivariate analysis using the geometric mean of analyte recoveries as the desirability function. Times of extraction and back-extraction of 300s and 100s, respectively, pH 5.5 at 30mmol/L acetate, 300µL of extraction solvent, and 600µmol/L of APDC were finally applied. Online interfacing to ICP-OES for back-extract analysis yielded average repeatabilities for Cd, Cu, and Pb of 2.9%, 3.5%, and 3.5% with limits of detections (3s) of 1.9, 1.4, and 5.6ng/mL, respectively. Oxidative back-extraction was proven reliable for the determination of metal species in coastal seawater, surrogate digestive fluids and soil leachates with recovery values for Cd, Cu, and Pb ranging from 90% to 118%, 68% to 104%, and 86% to 112%, respectively. Copyright © 2017 Elsevier B.V. All rights reserved.

  14. Bioassay requirements for 125I and 131I in medical, teaching and research institutions

    International Nuclear Information System (INIS)

    1983-09-01

    The more widespread use of radioactive isotopes of iodine (collectively referred to as radioiodines) as a research tool, coupled with their diagnostic and therapeutic uses in nuclear medicine, has resulted in an increased number of personnel who are exposed to these radioisotopes and who therefore should be monitored for internal radioiodine contamination. This document describes the minimum acceptable features of a bioassay programme which the Atomic Energy Control Board (AECB) requires to be available in institutions holding a prescribed substance licence authorising the use of significant quantities of 125 I or 131 I or both. A licensee may submit details of his own proposed bioassay programme to the AECB for approval. If such a programme fails to be approved, the programme described below shall be adhered to. This document does not deal with individuals who are likely to maintain a significant chronic thyroid burden of radioiodine. It is assumed that the radioiodine taken into the body is in a soluble, inorganic form (I 2 , iodide or iodate) or in an organic form (e.g. methyl iodide) which is metabolised in the body with a resultant release of iodide. Radioiodinated organic compounds which are not catabolised to iodide in the body to any significant degree are not the subject of this document, since the metabolism of the radioiodine will be dictated by the metabolism of the compound. This means that individuals whose only exposure to radioiodine is in the form of prepared radioiodinated compounds such as antigens and antibodies (e.g. individuals using radio immuno assay kits in which the antigen or antibody is supplied as radioiodinated material) are not required to participate in this bioassay programme for radioiodine

  15. Anion retention in soil: Possible application to reduce migration of buried technetium and iodine

    International Nuclear Information System (INIS)

    Gu, B.; Schulz, R.K.

    1991-10-01

    This report summarizes a literature review of our present knowledge of the anion exchange properties of a number of soils and minerals, which may potentially be used as anion exchangers to retard migration of such anions as iodide (I - ), iodate (IO 3 - ) and pertechnetate (TcO 4 - ) away from disposal site. The amorphous clays allophane and imogolite, are found to be among the most important soil components capable of developing appreciable amounts of positive charge for anion exchange even at about neutral pH. Decreases in the SiO 2 /Al 2 O 3 ratio and soil pH result in an increase in soil AEC. Allophane and imogolite rich soils have an AEC ranging from 1 to 18 meq/100g at pH about 6. Highly weathered soils dominated by Fe and Al oxides and kaolinite may develop a significant amount of AEC as soil pH falls. The retention of iodine (I) and technetium (T c ), by soils is associated with both soil organic matter, and Fe and Al oxides, whereas sorption on layer silicate minerals in negligible. Fe and Al oxides become more important in the retention of anionic I - , IO 3 - , and TcO 4 - as pH falls, since more positive charge is developed on the oxide surfaces. Although few studies, if any, have been conducted on I and T c sorption by soil allophane and imogolite, it is estimated that a surface plough soil (2 million pounds soil per acre) with 5 meq/100g AEC, as is commonly found in andisols, shall retain approximately 5900 kg I and 4500 kg T c . It is conceivable that an anion exchanger such as an andisol could be used to modify the near field environment of a radioactive waste disposal facility. This whole disposal system would then offer similar migration resistance to anions as is normally afforded to cations by usual and normal soils. 93 refs., 10 figs., 7 tabs

  16. The kinetic study of oxidation of iodine by hydrogen peroxide

    Energy Technology Data Exchange (ETDEWEB)

    Cantrel, L. [Institut de Protection et de Surete Nucleaire, IPNS, CEN Cadarache, Saint Paul lez Durance (France); Chopin, J. [Laboratoire d`Electrochimie Inorganique, ENSSPICAM, Marseille (France)

    1996-12-01

    Iodine chemistry is one of the most important subjects of research in the field of reactor safety because this element can form volatile species which represent a biological hazard for environment. As the iodine and the peroxide are both present in the sump of the containment in the event of a severe accident on a light water nuclear reactor, it can be important to improve the knowledge on the reaction of oxidation of iodine by hydrogen peroxide. The kinetics of iodine by hydrogen peroxide has been studied in acid solution using two different analytical methods. The first is a UV/Vis spectrophotometer which records the transmitted intensity at 460 nm as a function of time to follow the decrease of iodine concentration, the second is an amperometric method which permits to record the increase of iodine+1 with time thanks to the current of reduction of iodine+1 to molecular iodine. The iodine was generated by Dushman reaction and the series of investigations were made at 40{sup o}C in a continuous stirring tank reactor. The influence of the initial concentrations of iodine, iodate, hydrogen peroxide, H{sup +} ions has been determined. The kinetics curves comprise two distinct chemical phases both for molecular iodine and for iodine+1. The relative importance of the two processes is connected to the initial concentrations of [I{sub 2}], [IO{sub 3}{sup -}], [H{sub 2}O{sub 2}] and [H{sup +}]. A rate law has been determined for the two steps for molecular iodine. (author) figs., tabs., 22 refs.

  17. Effect of microorganisms on the chemical behavior of radionuclides in the environment

    International Nuclear Information System (INIS)

    Amachi, Seigo

    2004-01-01

    Microorganisms are affecting the fate of various radionuclides in the environment through processes such as sorption, accumulation, reduction, leaching and volatilization. We have studied on the microbial influences on the chemical behavior of iodine in the environment, and have isolated various microorganisms which can mediate volatilization, accumulation and oxidation of iodine. We found that iodine-volatilizing bacteria are distributed widely in the environment, and are very diverse group of bacteria. From gas chromatographic analyses, volatile iodine species produced by bacteria was identified as methyl iodide (CH 3 I). Radiotracer experiments were carried out to estimate bacterial contribution to the volatilization of iodine from soils and seawaters. In soil samples, bacteria were considered to play major roles in iodine volatilization since the addition of bacterial inhibitor almost completely inhibited the volatilization. On the other hand, in seawater samples, both bacterial and fungal (or algal) contributions were suggested. We also isolated iodine-accumulating bacteria and iodine-oxidizing bacteria from the environment. Iodine-accumulating bacteria were isolated from marine sediments, and 16S ribosomal DNA sequences showed that they are close to common marine bacteria Flexibacter sp. During the cultivation with iodide ion, they accumulated iodide intracellularly at a concentration that is more than 1,000 times higher than the culture medium. Iodide uptake by iodine-accumulating bacteria was found to occur biologically, and the uptake was specific for iodide but not for iodate. Iodine-oxidizing bacteria, which can mediate iodide (I - ) oxidation to molecular iodine (I 2 ), were phylogenetically divided into two groups within alpha-Proteobacteria, and iodide oxidation was mediated by an extracellular enzyme protein. (author)

  18. Chemical Engineering Division fuel cycle programs. Quarterly progress report, October-December 1978

    Energy Technology Data Exchange (ETDEWEB)

    Steindler, M J; Ader, M; Barletta, R E

    1980-01-01

    In the program on pyrochemical and dry processing methods (PDPM) for nuclear fuel, tungsten crucibles were successfully spun for use in laboratory-scale experiments. Corrosion testing of refractory metals and alloys in PDPM environments was done. Ceramic substrates were successfully coated with tungsten. Solubility measurements were made to determine Cd/Mg alloy composition and temperature at which dissolved Th will precipitate. Experiments were started to study the reduction of high-fired ThO/sub 2/ with Ca in a molten metal-molten salt system. Work on the fused salt electrolysis of CaO was started. Equipment for determining phase diagrams for U-Cu-Mg system was set up. The reaction of UO/sub 2/ with molten equimolar NaNO/sub 3/-KNO/sub 3/ was studied as part of a project to identify chemically feasible nonaqueous fuel reprocessing methods. Work was continued on development of a flowsheet for reprocessing actinide oxides by extracting actinides into ammonium chloro-aluminate (and alternative salts) from a bismuth solution. Preparation of Th, U, and Pu nitrides after dissolution of spent fuel elements in molten tin is being studied. Leach rates of glass beads, pulverized beads, and beads encapsulated in a lead matrix with no protective envelope were studied. A method (employing no pressure or vacuum systems) of encapsulating various solid wastes in a lead metal matrix was developed and tested. A preliminary integration was made of earlier data on effects of impacts on metal-matrix waste forms.Leach migration experiments were compared with conventional infiltration experiments as methods of evaluating geologic formations as barriers to nuclide migration. The effect of the streaming potential on the rates of transport of radioactive I/sup -/ and Na/sup +/ through kaolinite columns was measured, as well as adsorption of iodide and iodate by several compounds; implications of the results upon the disposal of radioactive iodine are discussed.

  19. Simultaneous determination of free and total glycerol in biodiesel by capillary electrophoresis using multiple short-end injection.

    Science.gov (United States)

    Spudeit, Daniel Alfonso; Piovezan, Marcel; Dolzan, Maressa D; Vistuba, Jacqueline Pereira; Azevedo, Mônia Stremel; Vitali, Luciano; Leal Oliveira, Marcone Augusto; Oliveira Costa, Ana Carolina; Micke, Gustavo Amadeu

    2013-12-01

    A rapid method for the simultaneous determination of free glycerol (FG) and total glycerol (TG) in biodiesel by CE using a short-end multiple injection (SE/MI) configuration system is described. The sample preparation for FG involves the extraction of glycerol with water and for TG a saponification reaction is carried out followed by extraction as in the case of FG. The glycerol extracted in both cases is submitted to periodate oxidation and the iodate ions formed are measured on a CE-SE/MI system. The relevance of this study lies in the fact that no analytical procedure has been previously reported for the determination of TG (or of FG and TG simultaneously) by CE. The optimum conditions for the saponification/extraction process were 1.25% KOH and 25°C, with a time of only 5 min, and biodiesel mass in the range of 50.0-200.0 mg can be used. Multiple injections were performed hydrodynamically with negative pressure as follows: 50 mbar/3s (FG sample); 50 mbar/6s (electrolyte spacer); 50 mbar/3s (TG sample). The linear range obtained was 1.55-46.5 mg/L with R(2) > 0.99. The LOD and LOQ were 0.16 mg/L and 0.47 mg/L, respectively for TG. The method provides acceptable throughput for application in quality control and monitoring biodiesel synthesis process. In addition, it offers simple sample preparation (saponification process), it can be applied to a variety biodiesel samples (soybean, castor, and waste cooking oils) and it can be used for the determination of two key parameters related to the biodiesel quality with a fast separation (less than 30 s) using an optimized CE-SE/MI system. © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  20. Assessing oxygen depletion in the Northeastern Pacific Ocean during the last deglaciation using I/Ca ratios from multiple benthic foraminiferal species

    Science.gov (United States)

    Taylor, M. A.; Hendy, I. L.; Chappaz, A.

    2017-08-01

    Paleo-redox proxies are crucial for reconstructing past bottom water oxygen concentration changes brought about by ocean circulation and marine productivity shifts in response to climate forcing. Carbonate I/Ca ratios of multiple benthic foraminifera species from Ocean Drilling Program Hole 1017E—a core drilled within the Californian oxygen minimum zone (OMZ), on the continental slope—are employed to reexamine the transition from the well-oxygenated last glacial into poorly oxygenated modern conditions. The redox and export productivity history of this site is constrained by numerous proxies used to assess sensitivity of I/Ca ratios of benthic foraminifera to changes in bottom and pore water O2 concentrations. Reconstructed iodate (IO3-) availability is from the I/Ca ratio of epifaunal (Cibicidoides sp.), shallow infaunal (Uvigerina peregrina), and deep infaunal (Bolivina spissa) foraminifera. The reconstructed IO3- availability profile is used to determine the contribution of bottom water O2 relative to oxidant demand on pore water O2 concentrations. These results suggest that high export productivity on the California Margin drove low pore water O2 concentrations during the Bølling. In contrast, low bottom water O2 concentrations at 950 m water depth only contributed to reduced sediments during the Allerød. Increased contribution of modified North Pacific Intermediate Water to the California Current System ventilated the California OMZ during the late glacial and the Younger Dryas such that water overlying the site was oxygenated. These results highlight the promising potential of this new proxy for understanding the relative influence of bottom water O2 concentration and pore water oxidant demand on OMZs.

  1. Elimination of suction effect in interfacing microchip electrophoresis with inductively coupled plasma mass spectrometry using porous monolithic plugs.

    Science.gov (United States)

    Cheng, Heyong; Liu, Jinhua; Yin, Xuefeng; Shen, Hong; Xu, Zigang

    2012-07-07

    A suction-free interfacing method was developed for microchip electrophoresis hyphenated with inductively coupled plasma mass spectrometry (MCE-ICP-MS). The hyphenated system was composed of a microchip, a demountable capillary microflow nebulizer (d-CMN) combined with a heated single pass spray chamber, a negative pressure sampling device, a high voltage power supply, a syringe pump and an ICP-MS. To eliminate the nebulizer suction generated by the pneumatic nebulizer and to ensure that the makeup solution flowed into the nebulizer, two porous polymer plugs were fabricated in the microchip. As a result, reasonably true electropherograms were obtained when compared to the CE separation performed in the traditional MCE-ICP-MS mode without porous polymer plugs. Electrophoretic separation of I(-) and IO(3)(-) was achieved within 25 s in a microchip with an effective separation length of only 15 mm at an electric field of 857 V cm(-1) using 10 mmol L(-1) borate (pH 9.2) as the running buffer. A resolution of 1.3 was obtained and the absolute detection limits for I(-) and IO(3)(-) were 0.12 and 0.13 fg, respectively. The precisions (RSD, n = 10) of the migration time and peak height for I(-) and IO(3)(-) were in the range of 1.1-1.6% and 2.5-2.8%, respectively. Two table salt samples were analyzed by an external calibration method. The iodate contents were in accordance with their labeled values. The recoveries of I(-) and IO(3)(-) in the table salt samples were in the range of 92-105%.

  2. Iodine binding to humic acid.

    Science.gov (United States)

    Bowley, H E; Young, S D; Ander, E L; Crout, N M J; Watts, M J; Bailey, E H

    2016-08-01

    The rate of reactions between humic acid (HA) and iodide (I(-)) and iodate (IO3(-)) have been investigated in suspensions spiked with (129)I at concentrations of 22, 44 and 88 μg L(-1) and stored at 10 °C. Changes in the speciation of (129)I(-), (129)IO3(-) and mixed ((129)I(-) + (129)IO3(-)) spikes were monitored over 77 days using liquid chromatography inductively coupled plasma mass spectrometry (LC-ICP-MS). In suspensions spiked with (129)I(-) 25% of the added I(-) was transformed into organic iodine (Org-(129)I) within 77 days and there was no evidence of (129)IO3(-) formation. By contrast, rapid loss of (129)IO3(-) and increase in both (129)I(-) and Org-(129)I was observed in (129)IO3(-)-spiked suspensions. However, the rate of Org-(129)I production was greater in mixed systems compared to (129)IO3(-)-spiked suspensions with the same total (129)I concentration, possibly indicating IO3(-)I(-) redox coupling. Size exclusion chromatography (SEC) demonstrated that Org-(129)I was present in both high and low molecular weight fractions of the HA although a slight preference to bond with the lower molecular weight fractions was observed indicating that, after 77 days, the spiked isotope had not fully mixed with the native (127)I pool. Iodine transformations were modelled using first order rate equations and fitted rate coefficients determined. However, extrapolation of the model to 250 days indicated that a pseudo-steady state would be attained after ∼200 days but that the proportion of (129)I incorporated into HA was less than that of (127)I indicating the presence of a recalcitrant pool of (127)I that was unavailable for isotopic mixing. Copyright © 2016 Elsevier Ltd. All rights reserved.

  3. Development of anion-exchange/reversed-phase high performance liquid chromatography-inductively coupled plasma-mass spectrometry methods for the speciation of bio-available iodine and bromine from edible seaweed.

    Science.gov (United States)

    Romarís-Hortas, Vanessa; Bermejo-Barrera, Pilar; Moreda-Piñeiro, Antonio

    2012-05-04

    Anion exchange high performance liquid chromatography hyphenated with inductively coupled plasma-mass spectrometry has been novelly applied to assess inorganic (iodide and iodate) and organic (3-iodotyrosine - MIT, and 3,5-diiodotyrosine - DIT) iodine species in a single chromatographic run. The optimized operating conditions (Dionex IonPac AS7, gradient elution with 175 mM ammonium nitrate plus 15% (v/v) methanol, pH 3.8, as a mobile phase and flow rates within the 0.5-1.5 mL min(-1) range) have also been used to perform inorganic bromine speciation analysis (bromide and bromate). The developed method has been applied for determining the bio-available contents of iodine and bromine species in dialyzates from edible seaweed. Reverse phase high performance liquid chromatography (Zorbax Eclipse XDB-C8, gradient elution with 0.2% (m/m) acetic acid, and 0.2% (m/m) acetic acid in methanol, as mobile phases, and a constant flow rate of 0.75 mL min(-1)) also hyphenated with inductively coupled plasma-mass spectrometry was used to confirm the presence of organic iodine species (MIT and DIT) in the dialyzates. The verification of the presence of iodinated amino acids (MIT and DIT) in the extracts was also performed by reverse phase high performance liquid chromatography-electrospray ionization-mass spectrometry (LTQ Orbitrap). The developed methods have provided good repeatability (RSD values lower than 10% for both anion exchange and reverse phase separations) and analytical recoveries within the 90-105% range for all cases. The in vitro bio-availability method consisted of a simulated gastric and an intestinal digestion/dialysis (10 kDa molecular weight cut-off - MWCO) two-stage procedure. Iodide and MIT were the main bio-available species quantified, whereas bromide was the major bromine species found in the extracts. Copyright © 2012 Elsevier B.V. All rights reserved.

  4. Electrocatalysis of anodic and cathodic oxygen-transfer reactions

    Energy Technology Data Exchange (ETDEWEB)

    Wels, B.R.

    1990-09-21

    The electrocatalysis of oxygen-transfer reactions is discussed in two parts. In Part I, the reduction of iodate (IO{sub 3}{sup {minus}}) is examined as an example of cathodic oxygen transfer. On oxide-covered Pt electrodes (PtO), a large cathodic current is observed in the presence of IO{sub 3}{sup {minus}} to coincide with the reduction of PtO. The total cathodic charge exceeds the amount required for reduction of PtO and IO{sub 3}{sup {minus}} to produce an adsorbed product. An electrocatalytic link between reduction of IO{sub 3}{sup {minus}} and reduction of PtO is indicated. In addition, on oxide-free Pt electrodes, the reduction of IO{sub 3}{sup {minus}} is determined to be sensitive to surface treatment. The electrocatalytic oxidation of CN{sup {minus}} is presented as an example of anodic oxygen transfer in Part II. The voltametric response of CN{sup {minus}} is virtually nonexistent at PbO{sub 2} electrodes. The response is significantly improved by doping PbO{sub 2} with Cu. Cyanide is also oxidized effectively at CuO-film electrodes. Copper is concluded to serve as an adsorption site for CN{sup {minus}}. It is proposed that an oxygen tunneling mechanism comparable to electron tunneling does not occur at the electrode-solution interface. The adsorption of CN{sup {minus}} is therefore considered to be a necessary prerequisite for oxygen transfer. 201 refs., 23 figs., 2 tabs.

  5. [Thyroid diseases in sub-Saharan Africa].

    Science.gov (United States)

    Sidibé, El Hassane

    2007-01-01

    hyperthyroidism has tripled, now accounting for 18.5% of all such operations. This disorder is found today in subjects older than 50 years, mainly from rural areas, and caused most often by Graves disease (25 of 51 cases). Graves disease in young women can cause serious problems during pregnancy; in such cases assessment of the minimal effective dose of antithyroid agents is essential. Carbimazole leads to remission in 61% of cases of Graves disease. Hypothyroidism can be auto-immune and often in patent forms because of insufficient screening in Africa: 24 cases in Dakar (1984) and 37 others noticed by us (1998). Single-nodule tumors were assessed in 89 patients in Khartoum: they were found to be simple goiters in 72% of cases, follicular adenoma in 13.5%, cancer in 13.5% (with 6 of the 12 cases follicular, 5 papillary, and 1 anaplastic). The sex ratio for thyroid cancer in Ouagadougou is 0.22, thus mainly women. It affects mainly women in their 30s. Thyroid cancer at Ibadan was found to be papillary carcinoma in 45.3% of cases; follicular forms were seen in 44.5% and this series includes 5% of medullary cancers (7 cases), with a mean age of 34 years. Already 4 other cases from Francophone sub-Saharan Africa have been noticed. Iodine deficiency is suggested to play a role because follicular cancer in southern Africa accounts for up to 55% of thyroid cancers. Thyroid cancers in Algeria are associated with low socioeconomic status and characterized by a high prevalence of cancers discovered at an advanced stage and of anaplastic carcinomas. Oral potassium iodate is recommended: 30 mg of iodate a month or 8 mg every two weeks. Iodized oil has been recommended by some authors, as well as a combination of iodine and sugar, and the iodation of drinking water; these are in addition to the proposed methods of opening up areas by new infrastructure). In conclusion, thyroid disease is due predominantly to iodine deficiency and goitrogenic products, but we also note the increasing emergence

  6. Final Report for research grant "Development of Methods for High Specific Activity Labeling of Biomolecules Using Astatine-211 in Different Oxidation States"

    Energy Technology Data Exchange (ETDEWEB)

    Wilbur, D. Scott [Univ. of Washington, Seattle, WA (United States)

    2011-12-14

    The overall objective of this research effort was to develop methods for labeling biomolecules with higher oxidation state species of At-211. This was to be done in an effort to develop reagents that had higher in vivo stability than the present carbon-bonded At-211-labeled compounds. We were unsuccessful in that effort, as none of the approaches studied provided reagents that were stable to in vivo deastatination. However, we gained a lot of information about At-211 in higher oxidation states. The studies proved to be very difficult as small changes in pH and other conditions appeared to change the nature of the species that obtained (by HPLC retention time analyses), with many of the species being unidentifiable. The fact that there are no stable isotopes of astatine, and the chemistry of the nearest halogen iodine is quite different, made it very difficult to interpret results of some experiments. With that said, we believe that a lot of valuable information was obtained from the studies. The research effort evaluated: (1) methods for chemical oxidation of At-211, (2) approaches to chelation of oxidized At-211, and (3) approaches to oxidation of astatophenyl compounds. A major hurdle that had to be surmounted to conduct the research was the development of HPLC conditions to separate and identify the various oxidized species formed. Attempts to develop conditions for separation of iodine and astatine species by normal and reversed-phase TLC and ITLC were not successful. However, we were successful in developing conditions (from a large number of attempts) to separate oxidized forms of iodine ([I-125]iodide, [I-125]iodate and [I-125]periodate) and astatine ([At-211]astatide, [At-211]astatate, [At-211]perastatate, and several unidentified At-211 species). Information on the basic oxidation and characterization of At-211 species is provided under Objective 1. Conditions were developed to obtain new At-211 labeling method where At-211 is chelated with the DOTA and

  7. Chemical and radiological toxicity of iodine isotopes. Experimental study on the rat at the perinatal stage; Toxicite chimique et radiologique des isotopes de l'iode. Etude experimentale chez le rat en periode perinatale

    Energy Technology Data Exchange (ETDEWEB)

    Bourahla, K

    2000-07-01

    The recommended prophylactic measure in the case of an exposure to radio-iodine is an excess take of stable iodine. During the perinatal stage, the thyroid is radio-sensible but also fragile with respect to an excess of iodine. This work performed on the rat, treats of the potential thyroidal toxicity of the prophylaxy and analyzes the early radio-lesions induced by {sup 131}I. On the basis of microscopic (optical, electronic, ionic) and dosimetric studies (TSH, T4), four aspects are considered: 1 - the perinatal morpho-functional evolution (F18, J1, J4, J10, J21, J35); 2 - the consequences of an iodine overburden at three moments of the thyroid maturation (F16, F20 and J4); 3 - the effects on the thyroid cells growth of different iodine overburdens (4 g, 20 g, 100 g); and 4 - the radio-toxic effects (after 48 h) of {sup 131}I taken at J5 (30 Gy) and at J35 (900 Gy). This work evidences the following points: 1 - the perinatal evolution of the thyroid tissue of the rat shows ultra-structural and follicular modifications and physiological follicular destructions; 2 - the variability of the iodine overburden effects: hyperactivity for overburdens at F16, tissue destruction with compensated hypothyroidism for overburdens at J5, no recognized thyroidal anomaly for the overburden at J20; 3 - the iodated overburden inhibits the start-up of the S-phase of the cellular cycle at a lower level (1/20); 4 - the {sup 131}I taken at J5 (30 Gy) induces a lysis of the nucleic acids content, while {sup 131}I taken at J35 (900 Gy) induces an important inflammatory reaction and some apoptosis phenomena. In summary, the stable iodine prophylactic measure can have two conjugated effects on the rat: an interesting action of thyroid cells growth inhibition, and a toxic action leading to an hyperactivity or a follicular destruction without hypothyroidism, depending on the maturation stage. The early effects of {sup 131}I seem to be linked with the age. (J.S.)

  8. Sorption, degradation, and transport of methyl iodide and other iodine species in geologic media

    International Nuclear Information System (INIS)

    Hu, Q.H.; Moran, J.E.; Gan, J.Y.

    2012-01-01

    Iodine is an important element in studies of human nutrition to combat I deficiency disorders, and in protection of the environment and human health from anthropogenic release of radioactive I. Biogeochemical cycling of I in the subsurface environment is complex, because it occurs in multiple oxidation states and as inorganic and organic species that may be volatile, hydrophilic and biophilic. Predicting the fate and transport of anthropogenic radioiodine deposited from the atmosphere or released into the subsurface requires knowledge of the sorption and degradation behavior of the various I species that may interact with soils and sediments. In this study, sorption, degradation, and transport behavior of I species (iodide, iodate, methyl iodide, and 4-iodoaniline) were examined in 12 geologic samples of differing physico-chemical characteristics, collected at numerous nuclear facilities in the USA. In particular, this work focuses on the sorption and degradation behavior of CH 3 I in geologic media, for which few studies are available, even though it is recognized as an important gaseous form of I in the marine atmosphere, and as a major form released from nuclear fuel reprocessing facilities and during nuclear accidents. Results from complementary batch and column experiments show that different I species exhibit very different sorption and transport behavior in geologic media. Sorption of I − is in general minimal, but a low concentration (5 × 10 −13 M) of radioactive 125 I is found to be strongly sorbed onto samples with high organic matter. Sorption of IO 3 - is consistently greater than that of I − , and sorption of 4-iodoaniline is generally strong and seems to be related to the amount of organic matter in the media. Methyl iodide is weakly sorbed onto 12 geologic samples with a distribution coefficient of about 1 mL/g, but its degradation varies greatly as a function of organic matter content, with a regression line of t 1/2 = 0.084 × OM + 0.088 (R

  9. Assessment of spatial variation in drinking water iodine and its implications for dietary intake: A new conceptual model for Denmark

    International Nuclear Information System (INIS)

    Voutchkova, Denitza Dimitrova; Ernstsen, Vibeke; Hansen, Birgitte; Sørensen, Brian Lyngby; Zhang, Chaosheng; Kristiansen, Søren Munch

    2014-01-01

    Iodine is essential for human health. Many countries have therefore introduced universal salt iodising (USI) programmes to ensure adequate intake for the populations. However, little attention has been paid to subnational differences in iodine intake from drinking water caused by naturally occurring spatial variations. To address this issue, we here present the results of a Danish nationwide study of spatial trends of iodine in drinking water and the relevance of these trends for human dietary iodine intake. The data consist of treated drinking water samples from 144 waterworks, representing approx. 45% of the groundwater abstraction for drinking water supply in Denmark. The samples were analysed for iodide, iodate, total iodine (TI) and other major and trace elements. The spatial patterns were investigated with Local Moran's I. TI ranges from < 0.2 to 126 μg L −1 (mean 14.4 μg L −1 , median 11.9 μg L −1 ). Six speciation combinations were found. Half of the samples (n = 71) contain organic iodine; all species were detected in approx. 27% of all samples. The complex spatial variation is attributed both to the geology and the groundwater treatment. TI > 40 μg L −1 originates from postglacial marine and glacial meltwater sand and from Campanian–Maastrichtian chalk aquifers. The estimated drinking water contribution to human intake varies from 0% to > 100% of the WHO recommended daily iodine intake for adults and from 0% to approx. 50% for adolescents. The paper presents a new conceptual model based on the observed clustering of high or low drinking-water iodine concentrations, delimiting zones with potentially deficient, excessive or optimal iodine status. Our findings suggest that the present coarse-scale nationwide programme for monitoring the population's iodine status may not offer a sufficiently accurate picture. Local variations in drinking-water iodine should be mapped and incorporated into future adjustment of the monitoring and/or the

  10. Assessment of spatial variation in drinking water iodine and its implications for dietary intake: A new conceptual model for Denmark

    Energy Technology Data Exchange (ETDEWEB)

    Voutchkova, Denitza Dimitrova, E-mail: ddv@geo.au.dk [Department of Geoscience, Aarhus University, Høegh-Guldbergs Gade 2, DK-8000 Aarhus C (Denmark); Geological Survey of Denmark and Greenland (GEUS), Lyseng Allé 1, DK-8270 Højbjerg (Denmark); Geological Survey of Denmark and Greenland (GEUS), Øster Voldgade 10, DK-1350 Copenhagen K (Denmark); Ernstsen, Vibeke [Geological Survey of Denmark and Greenland (GEUS), Øster Voldgade 10, DK-1350 Copenhagen K (Denmark); Hansen, Birgitte; Sørensen, Brian Lyngby [Geological Survey of Denmark and Greenland (GEUS), Lyseng Allé 1, DK-8270 Højbjerg (Denmark); Zhang, Chaosheng [GIS Centre and School of Geography and Archaeology, National University of Ireland, Galway (Ireland); Kristiansen, Søren Munch [Department of Geoscience, Aarhus University, Høegh-Guldbergs Gade 2, DK-8000 Aarhus C (Denmark)

    2014-09-15

    Iodine is essential for human health. Many countries have therefore introduced universal salt iodising (USI) programmes to ensure adequate intake for the populations. However, little attention has been paid to subnational differences in iodine intake from drinking water caused by naturally occurring spatial variations. To address this issue, we here present the results of a Danish nationwide study of spatial trends of iodine in drinking water and the relevance of these trends for human dietary iodine intake. The data consist of treated drinking water samples from 144 waterworks, representing approx. 45% of the groundwater abstraction for drinking water supply in Denmark. The samples were analysed for iodide, iodate, total iodine (TI) and other major and trace elements. The spatial patterns were investigated with Local Moran's I. TI ranges from < 0.2 to 126 μg L{sup −1} (mean 14.4 μg L{sup −1}, median 11.9 μg L{sup −1}). Six speciation combinations were found. Half of the samples (n = 71) contain organic iodine; all species were detected in approx. 27% of all samples. The complex spatial variation is attributed both to the geology and the groundwater treatment. TI > 40 μg L{sup −1} originates from postglacial marine and glacial meltwater sand and from Campanian–Maastrichtian chalk aquifers. The estimated drinking water contribution to human intake varies from 0% to > 100% of the WHO recommended daily iodine intake for adults and from 0% to approx. 50% for adolescents. The paper presents a new conceptual model based on the observed clustering of high or low drinking-water iodine concentrations, delimiting zones with potentially deficient, excessive or optimal iodine status. Our findings suggest that the present coarse-scale nationwide programme for monitoring the population's iodine status may not offer a sufficiently accurate picture. Local variations in drinking-water iodine should be mapped and incorporated into future adjustment of the

  11. Photoelectron Spectroscopy and Theoretical Studies of Anion-pi Interactions: Binding Strength and Anion Specificity

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Jian; Zhou, Bin; Sun, Zhenrong; Wang, Xue B.

    2015-01-01

    Proposed in theory and confirmed to exist, anion–π interactions have been recognized as new and important non-covalent binding forces. Despite extensive theoretical studies, numerous crystal structural identifications, and a plethora of solution phase investigations, intrinsic anion–π interaction strengths that are free from complications of condensed phases’ environments, have not been directly measured in the gas phase. Herein we present a joint photoelectron spectroscopic and theoretical study on this subject, in which tetraoxacalix[2]arene[2]triazine 1, an electron-deficient and cavity self-tunable macrocyclic was used as a charge-neutral molecular host to probe its interactions with a series of anions with distinctly different shapes and charge states (spherical halides Cl⁻, Br⁻, I⁻, linear thiocyanate SCN⁻, trigonal planar nitrate NO₃⁻, pyramidic iodate IO₃⁻, and tetrahedral sulfate SO₄²⁻). The binding energies of the resultant gaseous 1:1 complexes (1•Cl⁻,1•Br⁻, 1•I⁻, 1•SCN⁻, 1•NO₃⁻, 1•IO₃⁻ and 1•SO₄²⁻) were directly measured experimentally, exhibiting substantial non-covalent interactions with pronounced anion specific effects. The binding strengths of Cl⁻, NO₃⁻, IO₃⁻ with 1 are found to be strongest among all singly charged anions, amounting to ca. 30 kcal/mol, but only about 40% of that between 1 and SO₄²⁻. Quantum chemical calculations reveal that all anions reside in the center of the cavity of 1 with anion–π binding motif in the complexes’ optimized structures, where 1 is seen to be able to self-regulate its cavity structure to accommodate anions of different geometries and three-dimensional shapes. Electron density surface and natural bond orbital charge distribution analysis further support anion–π binding formation. The calculated binding energies of the anions and 1 nicely reproduce the experimentally estimated electron binding energy increase. This work

  12. Production of gaseous radiotracers CH{sub 3}I and I{sub 2} through Na{sup 123}I salt

    Energy Technology Data Exchange (ETDEWEB)

    Candeiro, R.E.M., E-mail: ricardocandeiro@cnen.gov.b [Comissao Nacional de Energia Nuclear (DIFOR/CNEN-CE), Fortaleza, CE (Brazil). Distrito de Fortaleza; Brandao, L.B. [Instituto de Engenharia Nuclear (IEN/CNEN-RJ), Rio de Janeiro, RJ (Brazil); Pereira, W.P. [Universidade Federal Fluminense (UFF), Niteroi, RJ (Brazil)

    2011-07-01

    The objective of the present work was to develop, separately, methodology for production of two gaseous tracers through the sodium iodide NaI marked with {sup 123}I. Found in the nature in form different, the iodine has been used in diverse works in the area of the industry and health. These two forms of the gaseous iodine, the methyl iodide, CH{sub 3}I, and molecular iodine, I{sub 2}, are very unstable and volatile in the ambient temperature and presents different problems in clean-up and monitoring systems. The syntheses were processed with sodium iodide (NaI) 1M aqueous solution marked with 1{sup 23I}. The production of gas I{sub 2} was realized with in chlorine acid (HCl) and sodium iodate salt (NaIO{sub 3}) and the CH{sub 3}I was used, the salt of NaI and the reagent (CH{sub 3}){sub 2}SO{sub 4}. The production of gases was initially realized through in unit in glass with an inert material and the purpose was to study the kinetic of reaction and to determine the efficiency of production. The two synthesis occurs in the reaction bottle and after of produced, the gas is stored in the collect bottle that contains a starch solution for fixed the I{sub 2}, and in syntheses of CH{sub 3}I contains a silver nitrate solution for your fixation. To determine the efficiency of production of gases, analytic tests were realized, where the consumption of iodide ions of the bottle of reaction are measured. The optimization of production of the each gaseous tracer was studied varying parameter as: concentration of iodide, concentration of acid and temperature. After, the syntheses of the radiotracers were realized in the compact unit, having been used as main reagent the salt radiated of sodium iodide, Na{sup 123}I. The transportation of elementary iodine and methyl iodine was studied by a scintillation detector NaI (2 x 2)' positioned in the reaction bottle. (author)

  13. Iodine adsorption on ion-exchange resins and activated carbons: batch testing

    International Nuclear Information System (INIS)

    Parker, Kent E.; Golovich, Elizabeth C.; Wellman, Dawn M.

    2014-01-01

    Iodine sorption onto seven resins and six carbon materials was evaluated using water from well 299-W19-36 on the Hanford Site. These materials were tested using a range of solution-to-solid ratios. The test results are as follows. The efficacy of the resin and granular activated carbon materials was less than predicted based on manufacturers' performance data. It is hypothesized that this is due to the differences in speciation previously determined for Hanford groundwater. The sorption of iodine is affected by the iodine species in the source water. Iodine loading on resins using source water ranged from 1.47 to 1.70 µg/g with the corresponding K d values from 189.9 to 227.0 mL/g. The sorption values when the iodine is converted to iodide ranged from 2.75 to 5.90 µg/g with the corresponding K d values from 536.3 to 2979.6 mL/g. It is recommended that methods to convert iodine to iodide be investigated in fiscal year (FY) 2015. The chemicals used to convert iodine to iodate adversely affected the sorption of iodine onto the carbon materials. Using as-received source water, loading and K d values ranged from 1.47 to 1.70 µg/g and 189.8 to 226.3 mL/g respectively. After treatment, loading and K d values could not be calculated because there was little change between the initial and final iodine concentration. It is recommended the cause of the decrease in iodine sorption be investigated in FY15. In direct support of CH2M HILL Plateau Remediation Company, Pacific Northwest National Laboratory has evaluated samples from within the 200W pump and treat bioreactors. As part of this analysis, pictures taken within the bioreactor reveal a precipitate that, based on physical properties and known aqueous chemistry, is hypothesized to be iron pyrite or chalcopyrite, which could affect iodine adsorption. It is recommended these materials be tested at different solution-to-solid ratios in FY15 to determine their effect on iodine sorption.

  14. Halogens in oil and gas production-associated wastewater.

    Science.gov (United States)

    Harkness, J.; Warner, N. R.; Dwyer, G. S.; Mitch, W.; Vengosh, A.

    2014-12-01

    surface water quality and drinking water utilities given the potential of formation of iodate-DBPs in drinking water. Olmstead, S.M. et al. (2013). Shale gas development impacts on surface water quality in Pennsylvania, PNAS, 110, 4962-4967.

  15. Synergetic effect of benzotriazole and non-ionic surfactant on copper chemical mechanical polishing in KIO{sub 4}-based slurries

    Energy Technology Data Exchange (ETDEWEB)

    Jiang, Liang [State Key Laboratory of Tribology, Tsinghua University, Beijing 100084 (China); Center for Advanced Materials Processing, Clarkson University, Potsdam, NY 13699 (United States); He, Yongyong [State Key Laboratory of Tribology, Tsinghua University, Beijing 100084 (China); Niu, Xiangyu; Li, Yuzhuo [Center for Advanced Materials Processing, Clarkson University, Potsdam, NY 13699 (United States); Luo, Jianbin, E-mail: luojb@tsinghua.edu.cn [State Key Laboratory of Tribology, Tsinghua University, Beijing 100084 (China)

    2014-05-02

    Ruthenium will be integrated into copper interconnects as a barrier layer in the near future. During the chemical mechanical polishing process of the ruthenium barrier layer, copper polishing performance with barrier slurries is crucial to microchips' final performance. This paper mainly studies the synergetic effect of benzotriazole (BTA) and non-ionic surfactant on copper polishing performance using KIO{sub 4}-based barrier slurries. The results show that, the copper removal rate (RR) and static etching rate increase with increasing concentration of KIO{sub 4} due to the increasing proportion of the Cu–periodate and Cu–iodate compounds like Cu(IO{sub 4}){sub 2} and Cu(IO{sub 3}){sub 2} of the passivating film on the copper surface; the added BTA can further enhance the copper RR instead of suppressing it probably due to the formation of incomplete Cu–BTA thin film. It is demonstrated that the combination of BTA and non-ionic surfactant exhibits excellent performance in suppressing the copper RR to about 200 Å/min, realizing satisfactory copper surface quality and achieving desirable material removal rate selectivity among copper, ruthenium and low-κ dielectrics. The synergetic passivation mechanism of BTA and non-ionic surfactant on the copper surface was investigated. It is proposed that in the presence of KIO{sub 4} as an oxidizer, the added BTA and non-ionic surfactant can form a porous passivating film on the copper surface which is mainly composed of the Cu–BTA complex, the adsorbed non-ionic surfactant and the leftover insoluble copper compounds like Cu(IO{sub 4}){sub 2} and Cu(IO{sub 3}){sub 2}, and then the hydrophobic polypropylene oxide segments of non-ionic surfactant can be effectively absorbed on the hydrophobic Cu–BTA complex as a supplement. The above two parts are integrated into a complete passivating film to protect the copper surface from chemical dissolution and excessive mechanical abrasion. - Highlights: • The copper

  16. Isotope excursions and shifting oxidation states recorded in the Paleoproterozoic Franceville Basin

    Science.gov (United States)

    Wang, V.; Junium, C. K.; Lu, Z.; Préat, A.

    2014-12-01

    Geochemical studies of Paleoproterozoic rocks have revealed that the initial rise of oxygen was protracted and that Earth's surface environments fluctuated between oxic and anoxic states over hundreds of millions of years. Marine sediments of the 2.1 Gyr-old Franceville Basin of west central Africa are only lightly metamorphosed, and their geochemistry may thus reveal unique insights into the environmental and metabolic conditions during the history of rising oxygen levels. In the Franceville Basin stratigraphic variation totaling 10‰ in δ13Ccarb was previously documented. This contribution builds on this work and characterizes changes in C, N, and S cycles using stable isotope values. The results from systematic analysis of several biologically mediated redox proxies preserved in carbonates from the Franceville Basin will be presented, including δ34S values of pyrite and δ13C and δ15N values of bulk organic carbon and kerogens. Consistent with independent reports of an excursion in δ13Corg in the Franceville Basin and elsewhere, we find ~20‰ stratigraphic variation in δ13C of bulk organic carbon. Initial results for δ15N of bulk organic matter range from -6 to 6 ‰, a wider distribution of values than previously reported for the Franceville Basin and more negative than values reported for the similarly aged Onega Basin in Fennoscandia. I/Ca ratios range from near zero to near Phanerozoic levels and are consistent with the presence of iodate. Chromium reducible sulfide has been extracted from all but one sample, confirming the presence of pyrite. δ34S of pyrite as well as δ13C and δ15N of kerogen will also be presented. The biochemically diverse array of proxy analyses presented here have varying thresholds of sensitivity to oxygen levels and hence will allow detailed reconstruction of the redox history of basin waters. As minimum O2 thresholds are often needed for certain biochemical processes, the resulting data will also have implications for key

  17. Iodine stability in salt double-fortified with iron and iodine.

    Science.gov (United States)

    Diosady, L L; Alberti, J O; Ramcharan, K; Mannar, M G Venkatesh

    2002-06-01

    Deficiencies in small quantities of micronutrients, especially iodine and iron, severely affect more than a third of the world's population, resulting in serious public health consequences, especially for women and young children. Salt is an ideal carrier of micronutrients. The double fortification of salt with both iodine and iron is an attractive approach to the reduction of both anemia and iodine-deficiency disorders. Because iodine is unstable under the storage conditions found during the manufacturing, distribution, and sale of salt in most developing countries, the effects of packaging materials and environmental conditions on the stability of salt double-fortified with iron and iodine were investigated. Salt was double-fortified with potassium iodide or potassium iodate and with ferrous sulfate or ferrous fumarate. The effects of stabilizers on the stability of iodine and iron were followed by storing the salt under three conditions that represent the extremes of normal distribution and sale for salt in developing countries: room temperature (25 degrees C) with 50%-70% relative humidity, 40 degrees C with 60% relative humidity, and 40 degrees C with 100% relative humidity. The effects of stabilizers, such as sodium hexametaphosphate (SHMP), calcium carbonate, calcium silicate, and dextrose were investigated. None of the combinations of iron and iodine compounds was stable at elevated temperatures. Essentially all of the iodine was lost over a period of six months. SHMP effectively slowed down the iodine loss, whereas magnesium chloride, a typical hygroscopic impurity, greatly accelerated this process. Calcium carbonate did not have a sparing effect on iodine, despite contrary indications in the literature. Ferrous sulfate-fortified salts generally turned yellow and developed an unpleasant rusty flavor. Salt fortified with ferrous fumarate and potassium, iodide was reasonably stable and maintained its organoleptic properties, making it more likely to be

  18. Effect of maternal excessive iodine intake on neurodevelopment and cognitive function in rat offspring

    Directory of Open Access Journals (Sweden)

    Zhang Le

    2012-10-01

    Full Text Available Abstract Background Iodine deficiency and iodine excess are both associated with adverse health consequences. Iodine deficiency during pregnancy leads to insufficient maternal thyroid hormone, subsequently causing irreversible adverse effects on the neurological and cognitive functions of the offspring. The results of our previous epidemiological study suggested that mild iodine excess might increase the prevalence of subclinical hypothyroidism. In the present study, female Wistar rats maintained on low-iodine grain were randomly assigned to three groups based on iodated water concentration: low iodine (LI, 1.2 μg/d, normal iodine (NI, 5–6 μg/d, and 3-fold high iodine (3HI, 15–16 μg/d. The present study investigated whether higher-than-normal iodine intake (3HI by rats from before pregnancy until breastfeeding affects the postnatal (PN neurodevelopment (PN7 and PN45 of their offspring during particularly sensitive periods in brain development. Results After 12 weeks of treatment (before pregnancy, iodine concentrations in urine and thyroid tissue and circulating thyroxine of adult females correlated with iodine intake. Brain-derived neurotrophic factor (BDNF expression in the hippocampi of pups on PN7 and PN45 was decreased in 3HI group compared to the NI controls (P  0.05, all On PN7 and PN45, the BDNF levels of the 3HI pups were 83.5% and 88.8%, respectively, that of the NI pups. In addition, the 3HI group had a higher neuroendocrine-specific protein A (NSP-A level than the NI controls on PN7 (P  0.05. NSP-A levels of the 3HI pups were 117.0% that of the NI pups. No significant difference was observed in the expressions of c-Fos or c-Jun in the hippocampal CA1 region of the 3HI group compared to the controls (P > 0.05. Results from the Morris water maze test revealed that pups of the 3HI group had mild learning and spatial memory deficits. Conclusions The neurodevelopmental and cognitive deficits of the 3HI pups were

  19. Anion retention in soil: Possible application to reduce migration of buried technetium and iodine

    Energy Technology Data Exchange (ETDEWEB)

    Gu, B.; Schulz, R.K. (California Univ., Berkeley, CA (United States). Dept. of Soil Science)

    1991-10-01

    This report summarizes a literature review of our present knowledge of the anion exchange properties of a number of soils and minerals, which may potentially be used as anion exchangers to retard migration of such anions as iodide (I{sup {minus}}), iodate (IO{sub 3}{sup {minus}}) and pertechnetate (TcO{sub 4}{sup {minus}}) away from disposal site. The amorphous clays allophane and imogolite, are found to be among the most important soil components capable of developing appreciable amounts of positive charge for anion exchange even at about neutral pH. Decreases in the SiO{sub 2}/Al{sub 2}O{sub 3} ratio and soil pH result in an increase in soil AEC. Allophane and imogolite rich soils have an AEC ranging from 1 to 18 meq/100g at pH about 6. Highly weathered soils dominated by Fe and Al oxides and kaolinite may develop a significant amount of AEC as soil pH falls. The retention of iodine (I) and technetium ({Tc}), by soils is associated with both soil organic matter, and Fe and Al oxides, whereas sorption on layer silicate minerals in negligible. Fe and Al oxides become more important in the retention of anionic I{sup {minus}}, IO{sub 3}{sup {minus}}, and TcO{sub 4}{sup {minus}} as pH falls, since more positive charge is developed on the oxide surfaces. Although few studies, if any, have been conducted on I and {Tc} sorption by soil allophane and imogolite, it is estimated that a surface plough soil (2 million pounds soil per acre) with 5 meq/100g AEC, as is commonly found in andisols, shall retain approximately 5900 kg I and 4500 kg {Tc}. It is conceivable that an anion exchanger such as an andisol could be used to modify the near field environment of a radioactive waste disposal facility. This whole disposal system would then offer similar migration resistance to anions as is normally afforded to cations by usual and normal soils. 93 refs., 10 figs., 7 tabs.

  20. Airborne waste management technology applicable for use in reprocessing plants for control of iodine and other off-gas constituents

    International Nuclear Information System (INIS)

    Jubin, R.T.

    1988-02-01

    Extensive work in the area of iodine removal from reprocessing plant off-gas streams using various types of solid sorbent materials has been conducted worldwide over the past two decades. This work has focused on the use of carbon filters, primarily for power plant applications. More recently, the use of silver-containing sorbents has been the subject of considerable research. The most recent work in the United States has addressed the use of silver-exchanged faujasites and mordenites. The chemical reactions of iodine with silver on the sorbent are not well defined, but it is generally believed that chemisorbed iodides and iodates are formed. The process for iodine recovery generally involves passage of the iodine-laden gas stream through a packed bed of the adsorbent material preheated to a temperature of about 150/degree/C. Most iodine removal system designs utilizing silver-containing solid sorbents assume only a 30 to 50% silver utilization. Based on laboratory tests, potentially 60 to 70% of the silver contained in the sorbents can be reacted with iodine. To overcome the high cost of silver associated with these materials, various approaches have been explored. Among these are the regeneration of the silver-containing sorbent by stripping the iodine and trapping the iodine on a sorbent that has undergone only partial silver exchange and is capable of attaining a much higher silver utilization. This summary report describes the US work in regeneration of iodine-loaded solid sorbent material. In addition, the report discusses the broader subject of plant off-gas treatment including system design. The off-gas technologies to recovery No/sub x/ and to recover and dispose of Kr, 14 C, and I are described as to their impacts on the design of an integrated off-gas system. The effect of ventilation philosophy for the reprocessing plant is discussed as an integral part of the overall treatment philosophy of the plant off-gas. 103 refs., 5 figs., 8 tabs

  1. Radio-active colloids in the functional exploration of the reticulo-endothelium system

    International Nuclear Information System (INIS)

    Chivot, J.J.

    1967-03-01

    A historical review describes the reticulo-endothelial system (R.E.S.) and aims at defining it and at explaining its operation. The methods used for its examination and the colloids utilized are considered. The author has been led to prepare a special type of colloid: an albuminous complex containing radio-iodine, 'C.A. 131 I', whose method of preparation and physical and biological examination are described. A human albumin, having a known optical density in solution, is heated until a change in the optical density indicates that an aggregation of the proteinic molecules has occurred. The denatured protein is iodated with 131 I. Electrophoretic, ultracentrifuge and autoradiographic controls are then carried out. This atoxic and metabolisable preparation of biological origin is compared with the better defined colloidal gold which serves as reference. C.A. 131 I is injected into mice. It is shown by radioactivity measurements, auto-radiographies on sections of the whole animal, and anthropo-gamma-metric detections that a high concentration occurs in the S.R.E. of the liver. These static results are only of limited importance however compared to those obtained from an in vivo study of the phenomenon. The author records the changes in the radioactivity of the blood derived from the carotid artery using a well-scintillator. He obtains directly a curve of the radioactivity of blood having a decreasing exponential form; the mathematical expression describing this curve is given. The biological half-life T 1/2 of the colloid in the blood is a measure of its phagocytosis by the S.R.E. cells. A supplementary check is provided by the direct recording of the hepatic activity using a suitably collimated exterior detector. A curve of increasing-exponential form is obtained and its parameters are corollary to the preceding curve. These tests carried out on guinea-pigs and rats make it possible to give to the S.R.E. a phagocytic index which is characteristic of its state of

  2. Spectrophotometric determination of peptic ulcer sulfur-containing drugs in bulk form and in tablets.

    Science.gov (United States)

    Mohamed, Gehad G; Nour El-Dien, F A; Khalil, Shaban M; El-Tantawy, Aliaa S M

    2010-01-01

    Two spectrophotometric procedures are suggested for the determination of three irreversible proton pump inhibitors, rabeprazole (RAB), omeprazole (OMP) and pantoprazole (PAN) in pure form and in different pharmaceutical formulations. The first method is based on the oxidation of RAB and PAN with potassium iodate in an acidic medium followed by extracting the liberated iodine with cyclohexane and measurement at λ = 520 nm. Beer's law is valid in the concentration ranges from 10-400 and 5-400 µg ml(-1) for RAB and PAN, respectively. The apparent molar absorptivities of the resulting coloured product were found to be 1.34 × 10(3) and 1.64 × 10(3) l.mol(-1). cm(-1) for RAB and PAN, respectively. The second method is based on the interaction of the basic drugs, OMP, RAB and PAN, in 1,2-dichloroethane with bromophenol blue (BPB), bromocresol green (BCG) and bromocresol purple (BCP) in the same solvent to produce stable coloured ion pairs with maximum absorbance at 385-405 nm. Regression analysis of Beer's plots showed good correlation in the concentration ranges 10-60, 10-60 and 5-40 µg ml(-1) for OMP, 10-150, 10-150 and 10-60 µg ml(-1) for RAB and 10-250, 10-150 and 10-100 µg ml(-1) for PAN with BPB, BCG and BCP reagents, respectively. The limits of detection are 0.46-7.69 µg ml(-1) and limits of quantitation range between 1.52-8.53 µg ml(-1). The optimum assay conditions were investigated and the recovery of the drugs from their dosage forms ranged from 99.33% to 100.5%. Intraday relative standard deviations (RSD) were 0.029-1.397% and the correlation coefficients ranged from 0.9992 to 1. The two methods can be applied successfully for the determination of these drugs in tablets. The results of analysis were validated statistically through recovery studies. © 2009 John Wiley & Sons, Ltd.

  3. Iodine adsorption on ion-exchange resins and activated carbons: batch testing

    Energy Technology Data Exchange (ETDEWEB)

    Parker, Kent E.; Golovich, Elizabeth C.; Wellman, Dawn M.

    2014-09-30

    Iodine sorption onto seven resins and six carbon materials was evaluated using water from well 299-W19-36 on the Hanford Site. These materials were tested using a range of solution-to-solid ratios. The test results are as follows. The efficacy of the resin and granular activated carbon materials was less than predicted based on manufacturers’ performance data. It is hypothesized that this is due to the differences in speciation previously determined for Hanford groundwater. The sorption of iodine is affected by the iodine species in the source water. Iodine loading on resins using source water ranged from 1.47 to 1.70 µg/g with the corresponding Kd values from 189.9 to 227.0 mL/g. The sorption values when the iodine is converted to iodide ranged from 2.75 to 5.90 µg/g with the corresponding Kd values from 536.3 to 2979.6 mL/g. It is recommended that methods to convert iodine to iodide be investigated in fiscal year (FY) 2015. The chemicals used to convert iodine to iodate adversely affected the sorption of iodine onto the carbon materials. Using as-received source water, loading and Kd values ranged from 1.47 to 1.70 µg/g and 189.8 to 226.3 mL/g respectively. After treatment, loading and Kd values could not be calculated because there was little change between the initial and final iodine concentration. It is recommended the cause of the decrease in iodine sorption be investigated in FY15. In direct support of CH2M HILL Plateau Remediation Company, Pacific Northwest National Laboratory has evaluated samples from within the 200W pump and treat bioreactors. As part of this analysis, pictures taken within the bioreactor reveal a precipitate that, based on physical properties and known aqueous chemistry, is hypothesized to be iron pyrite or chalcopyrite, which could affect iodine adsorption. It is recommended these materials be tested at different solution-to-solid ratios in FY15 to determine their effect on iodine

  4. Extended networks, porous sheets, and chiral frameworks. Thorium materials containing mixed geometry anions: Structures and properties of Th(SeO3)(SeO4), Th(IO3)2(SeO4)(H2O)3.H2O, and Th(CrO4)(IO3)2

    International Nuclear Information System (INIS)

    Sullens, Tyler A.; Almond, Philip M.; Byrd, Jessica A.; Beitz, James V.; Bray, Travis H.; Albrecht-Schmitt, Thomas E.

    2006-01-01

    Three novel Th(IV) compounds containing heavy oxoanions, Th(SeO 3 )(SeO 4 ) (1), Th(IO 3 ) 2 (SeO 4 )(H 2 O) 3 .H 2 O (2), and Th(CrO 4 )(IO 3 ) 2 (3), have been synthesized under mild hydrothermal conditions. Each of these three distinct structures contain trigonal pyramidal and tetrahedral oxoanions. Compound 1 adopts a three-dimensional structure formed from ThO 9 tricapped trigonal prisms, trigonal pyramidal selenite, SeO 3 2- , anions containing Se(IV), and tetrahedral selenate, SeO 4 2- , anions containing Se(VI). The structure of 2 contains two-dimensional porous sheets and occluded water molecules. The Th centers are found as isolated ThO 9 tricapped trigonal prisms and are bound by four trigonal pyramidal iodate anions, two tetrahedral selenate anions, and three coordinating water molecules. In the structure of 3, the Th(IV) cations are found as ThO 9 tricapped trigonal prisms. Each Th center is bound by six IO 3 1- anions and three CrO 4 2- anions forming a chiral three-dimensional structure. Second-harmonic generation of 532nm light from 1064nm radiation by a polycrystalline sample of 3 was observed. Crystallographic data (193K, MoKα, λ=0.71073): 1; monoclinic, P2 1 /c; a=7.0351(5)A, b=9.5259(7)A, c=9.0266(7)A, β=103.128(1), Z=4, R(F)=2.47% for 91 parameters with 1462 reflections with I>2σ(I); 2, monoclinic, P2 1 /n, a=7.4889(9)A, b=8.002(1)A, c=20.165(3)A, β=100.142(2), Z=4, R(F)=4.71% for 158 parameters with 2934 reflections with I>2σ(I); 3, orthorhombic, P2 1 2 1 2 1 , a=7.3672(5)A, b=9.3617(6)A, c=11.9201(7)A, Z=4, R(F)=2.04% for 129 parameters with 2035 reflections with I>2σ(I)

  5. Oxidative removal of implanted photoresists and barrier metals in semiconductor processing

    Science.gov (United States)

    Govindarajan, Rajkumar

    Chemical systems containing oxidants are widely used at various stages in semiconductor processing, particularly for wet cleaning and polishing applications. This dissertation presents a series of studies related to oxidative removal of materials in the Front-End-Of-Line (FEOL) and Chemical Mechanical Planarization (CMP) processes during IC fabrication. In the first part of this study, stripping of photoresists exposed to high dose of ions (1E16 As/cm2) was investigated in activated hydrogen peroxide systems. Stripping of photoresists (PR) exposed to high dose (>1E15/cm2) ion beams is one of the most challenging steps in FEOL processing. This is due to unreactive crust layer that forms on the resist surface during ion implantation. The use of hydrogen peroxide systems activated by metal ion or UV light, for disrupting crust formed on deep UV resist to enable complete removal of crust as well as underlying photoresist was investigated. A systematic evaluation of variables such as hydrogen peroxide and metal ion concentration, UV intensity, temperature and time was conducted and an optimal formulation capable of attacking the crust was developed. A two step process involving pretreatment with activated hydrogen peroxide solution, followed by treatment with sulfuric acid-hydrogen peroxide mixture (SPM) was developed for complete removal of crusted resist films. In the second part of this study, electrochemically enhanced abrasive removal of Ta/TaN films was investigated in solutions containing 2,5 dihydroxy benzene sulfonic acid (DBSA) and potassium iodate (KIO3). This method known as Electrically-assisted Chemical Mechanical Planarization (ECMP) is generating a lot of interest in IC manufacturing. Ta/TaN films were abraded at low pressures (polyurethane pad under galvanostatic conditions. The effect of variables including pH, KIO3 concentration, and current density has been explored. In the optimized formulation, tantalum and tantalum nitride removal rates of ˜170 A

  6. Effect of different oxidants on polyaniline/single walled carbon nanotubes composites synthesized via ultrasonically initiated in-situ chemical polymerization

    Energy Technology Data Exchange (ETDEWEB)

    Gull, Nafisa, E-mail: gullchemist@gmail.com [Department of Polymer Engineering and Technology, University of the Punjab, Lahore, 54590 (Pakistan); Khan, Shahzad Maqsood, E-mail: shahzadkhan81@hotmail.com [Department of Polymer Engineering and Technology, University of the Punjab, Lahore, 54590 (Pakistan); Islam, Atif; Zia, Saba; Shafiq, Muhammad; Sabir, Aneela; Munawar, Muhammad Azeem [Department of Polymer Engineering and Technology, University of the Punjab, Lahore, 54590 (Pakistan); Butt, Muhammad Taqi Zahid [College of Engineering and Emerging Technologies, University of the Punjab, Lahore, 54590 (Pakistan); Jamil, Tahir [Department of Polymer Engineering and Technology, University of the Punjab, Lahore, 54590 (Pakistan)

    2016-04-01

    This study is aimed at investigating the effect of different oxidants on properties of polyaniline/single walled carbon nanotubes (PANI/SWCNT) composites and scrutinizing a suitable oxidant to improve the properties of composites. PANI/SWCNT composites were fabricated via ultrasonically initiated in-situ chemical polymerization technique using four different oxidants; hydrogen peroxide (H{sub 2}O{sub 2}), ammonium peroxidisulphate ((NH{sub 4}){sub 2}S{sub 2}O{sub 8}), potassium dichromate (K{sub 2}Cr{sub 2}O{sub 7}) and potassium iodate (KIO{sub 3}). Percent yield (97%), molecular weight (45532 g mol{sup −1}) and electrical conductivity (0.835 S cm{sup −1}) were found maximum for composite prepared in the presence of H{sub 2}O{sub 2}. Structural confirmation of PANI and charge transfer complex formation between PANI and SWCNT were confirmed by fourier transform infrared spectroscopy, UV–visible spectroscopy and X-ray diffraction spectroscopy. Thermogravimetric analysis verified that the PANI/SWCNT composite synthesized using H{sub 2}O{sub 2} had maximum thermal stability with least thermal degradation (∼28%). Minimal thermal transitions of the composite were also observed for same composite by differential scanning calorimetry. Scanning electron microscopic images of PANI/SWCNT composites revealed that SWCNT were properly dispersed in PANI matrix when H{sub 2}O{sub 2} was used. Above results provide the valuable suggestion that; H{sub 2}O{sub 2} is a promising oxidant to enhance structural, thermal, electrical and microscopic properties of composites. - Highlights: • Ultrasonically initiated in-situ chemical polymerization protocol was devised for synthesis of PANI/SWCNT composites. • SEM micrographs of PANI/SWCNT-1 showed uniform dispersed structure. • Better thermal stability and conductivity was evidenced for H{sub 2}O{sub 2} based PANI/SWCNT composite. • π–π interaction between PANI and SWCNT is confirmed by FTIR and UV

  7. Presença de ovos de Toxocara spp em praças públicas da cidade de Uberlândia, Minas Gerais, Brasil Presence of Toxocara spp eggs in public squares of Uberlândia city, Minas Gerais, Brazil

    Directory of Open Access Journals (Sweden)

    Julia Maria Costa-Cruz

    1994-02-01

    Full Text Available O objetivo deste trabalho foi verificar a presença de ovos de Toxocara spp nos solos de praças públicas da cidade de Uberlândia, região do Triângulo Mineiro, no período de outubro de 1991 a janeiro de 1992. A cidade possui 89 praças distribuídas em 39 bairros. Para que se tivesse um perfil da ocorrência do parasita, foram colhidas amostras de terra e areia (quando existente de uma praça, determinada por sorteio, por bairro. As amostras de solo homogeneizadas de 5 pontos distintos das 39 praças foram colhidas em frascos plásticos e analisadas empregando-se os métodos de flutuação em solução saturada de cloreto de sódio e de solução saturada de sulfato de magnésio contendo 5% de iodeto de potássio. Para cada amostra foram realizados os dois métodos em duplicata. Os resultados mostraram estarem contaminados os solos de 9 praças (23,07%, das quais 6 localizavam-se próximas ao centro da cidade. A realização de mais de um método laboratorial permitiu a identificação do agente em maior porcentagem de locais.The objective of this study was to verify the presence of Toxocara spp eggs in the public squares ground in Uberlândia, region of Triângulo Mineiro, from October 1991 to January 1992. The city has 89 squares distributed in 39 boroughs. In order to have an outline of the parasite's occurrence, ground and sand (when existent samples were collected from one square per boroughors. The squares were determined by draw. The homogenized ground samples of distinct points of the 39 squares, were colected in plastic flasks and analysed by the methods of fluctuation in sodium chloride saturated solution and magnesium sulphate saturated solution which contained 5% of potassium iodate. Both methods were executed twice for each sample. The results showed that the ground of 9 squares (23.07% was contaminated, 6 of which were located near downtown. The execution of more than one laboratorial method permited the agent's identification

  8. Chemical Engineering Division fuel cycle programs. Quarterly progress report, April-June 1979. [Pyrochemical/dry processing; waste encapsulation in metal; transport in geologic media

    Energy Technology Data Exchange (ETDEWEB)

    Steindler, M.J.; Ader, M.; Barletta, R.E.

    1980-09-01

    For pyrochemical and dry processing materials development included exposure to molten metal and salt of Mo-0.5% Ti-0.07% Ti-0.01% C, Mo-30% W, SiC, Si/sub 2/ON/sub 2/, ZrB/sub 2/-SiC, MgAl/sub 2/O/sub 4/, Al/sub 2/O/sub 3/, AlN, HfB/sub 2/, Y/sub 2/O/sub 3/, BeO, Si/sub 3/N/sub 4/, nickel nitrate-infiltrated W, W-coated Mo, and W-metallized alumina-yttria. Work on Th-U salt transport processing included solubility of Th in liquid Cd, defining the Cd-Th and Cd-Mg-Th phase diagrams, ThO/sub 2/ reduction experiments, and electrolysis of CaO in molten salt. Work on pyrochemical processes and associated hardware for coprocessing U and Pu in spent FBR fuels included a second-generation computer model of the transport process, turntable transport process design, work on the U-Cu-Mg system, and U and Pu distribution coefficients between molten salt and metal. Refractory metal vessels are being service-life tested. The chloride volatility processing of Th-based fuel was evaluated for its proliferation resistance, and a preliminary ternary phase diagram for the Zn-U-Pu system was computed. Material characterization and process analysis were conducted on the Exportable Pyrochemical process (Pyro-Civex process). Literature data on oxidation of fissile metals to oxides were reviewed. Work was done on chemical bases for the reprocessing of actinide oxides in molten salts. Flowsheets are being developed for the processing of fuel in molten tin. Work on encapsulation of solidified radioactive waste in metal matrix included studies of leach rate of crystalline waste materials and of the impact resistance of metal-matrix waste forms. In work on the transport properties of nuclear waste in geologic media, adsorption of Sr on oolitic limestone was studied, as well as the migration of Cs in basalt. Fitting of data on the adsorption of iodate by hematite to a mathematical model was attempted.

  9. Yucca Mountain Project Getter Program Results (Year 1) I-I29 and Other Anions of Concern

    Energy Technology Data Exchange (ETDEWEB)

    J.L. Krumhansl; J.D. Pless; J.B. Chwirka; K.C. Holt

    2006-07-17

    Although high level nuclear wastes (HLW) contain a daunting array of radioisotopes, only a restricted number are long-lived enough to be problematic, and of these many are either effectively insoluble or are likely to be scavenged from solution by minerals indigenous to all aquifers. Those few constituents likely to travel significant distances through aquifers either form colloids (and travel as particulates) or anions--which are not sorbed onto the predominantly negatively charged mineral surfaces. Iodine ({sup 129}I) is one such constituent and may travel as either iodide (I{sup -}) or iodate (IO{sub 3}{sup -}) depending on whether conditions are mildly reducing or oxidizing. Conventionally, {sup 99}Tc (traveling as TcO{sub 4}{sup 0}) is regarded as being of greater concern since it is both more abundant and has a shorter half life (e.g., has a higher specific activity). However, it is unclear whether TcO{sub 4}{sup -} will ever actually form in the mildly reducing environments thought likely within degrading HLW canisters. Instead, technetium may remain reduced as highly insoluble Tc(lV), in which case {sup 129}I might become a significant risk driver in performance assessment (PA) calculations. In the 2004-2005 time frame the US Department of Energy (DOE)--Office of Civilian Radioactive Waste Management (OCRUM), Office of Science and Technology International (S&T) funded a program to identify ''getters'' for possible placement in the invert beneath HLW packages in the repository being planned by the Yucca Mountain Project (YMP). This document reports on progress made during the first (and only) year of this activity. The problem is not a new one and the project did not proceed in a complete vacuum of information. Potential leads came from past studies directed at developing anion getters for a near surface low-level waste facility at Hanford, which suggested that both copper-containing compounds and hydrotalcite-group minerals might be

  10. Yucca mountain project getter program results(year 1):I-129 and other anions of concern.

    Energy Technology Data Exchange (ETDEWEB)

    Krumhansl, James Lee; Pless, Jason; Chwirka, J. Benjamin

    2006-07-01

    Although high level nuclear wastes (HLW) contain a daunting array of radioisotopes, only a restricted number are long-lived enough to be problematic, and of these many are either effectively insoluble or are likely to be scavenged from solution by minerals indigenous to all aquifers. Those few constituents likely to travel significant distances through aquifers either form colloids (and travel as particulates) or anions--which are not sorbed onto the predominantly negatively charged mineral surfaces. Iodine ({sup 129}I) is one such constituent and may travel as either iodide (I{sup -}) or iodate (IO{sub 3}{sup -}) depending on whether conditions are mildly reducing or oxidizing. Conventionally, {sup 99}Tc (traveling as TcO{sub 4}{sup -}) is regarded as being of greater concern since it is both more abundant and has a shorter half life (e.g., has a higher specific activity). However, it is unclear whether TcO{sub 4}{sup -} will ever actually form in the mildly reducing environments thought likely within degrading HLW canisters. Instead, technetium may remain reduced as highly insoluble Tc(IV), in which case {sup 129}I might become a significant risk driver in performance assessment (PA) calculations. In the 2004-2005 time frame the US Department of Energy (DOE)--Office of Civilian Radioactive Waste Management (OCRUM), Office of Science and Technology International (S&T) funded a program to identify ''getters'' for possible placement in the invert beneath HLW packages in the repository being planned by the Yucca Mountain Project (YMP). This document reports on progress made during the first (and only) year of this activity. The problem is not a new one and the project did not proceed in a complete vacuum of information. Potential leads came from past studies directed at developing anion getters for a near surface low-level waste facility at Hanford, which suggested that both copper-containing compounds and hydrotalcite-group minerals might be

  11. PENGUJIAN NETRALISASI SIFAT REAKTIF BUMBU DALAM GARAM BERYODIUM DENGAN BAHAN TAMBAHAN MAKANAN

    Directory of Open Access Journals (Sweden)

    Suryana Purawisastra

    2012-11-01

    not allof them, these were for CaC03 K-citrate, and benzoic acid. It was shown by the value of recovery of potassiumiodate contents of the iodized salt. The netralization properties of food addives were increased by the increasing of the potassiumiodate content of the iodized salt.Conclusions: The addition of some food additives into the iodized salt is able to prevent the iodate content of the salt from there activity of subtances in the spice. The addition of food additives also can pick up moisture of salt resulting preventation of the salt particles clumping together and so keep the product free flowing.Keywords: potassiumiodate, spices, iodized salt

  12. Study on Radioecology and Tracer of Iodine-129

    International Nuclear Information System (INIS)

    Xiaolin, Hou

    2004-01-01

    Chernobyl contaminated regions. The investigations show a strong dependence of childhood thyroid cancer incidence on thyroid exposure dose from short-lived radioiodine isotopes (i.e. 131 I, 133 I) released from the Chernobyl accident. However, the short half-life of 133 I (20.8 h) and 131 I (8.02 d) makes the evaluation of thyroid dose from these isotopes not easy. Due to the long half-life of 129 I, the 129 I concentration in environmental samples can be used to reconstruct the 131 I and 133 I dose to thyroids. Soil samples from areas in Belarus, Russia and Sweden contaminated by the Chernobyl accident were analysed for 129 I and 137 Cs by gamma-spectrometry. The atomic ratios of 129 I/ 137 Cs ranged from 0.10 to 0.30, with an average of 0.18. It confirmed that the 129 I/ 137 Cs ratios could be to reconstruct the deposition pattern of 131 I in these areas. (3) Application of I-129 as an oceanographic tracer. By analysing the time series seaweed samples collected from the coast of Denmark, Norway, and west Greenland, seawater samples from Baltic Sea, North Sea, Belt Sea, lake water from Denmark and other Baltic Seas for 129 I and 127 I, the transportation, mixing and water mass from North Sea to North Atlantic, Arctic and Baltic Sea and the origination of I-129 in the Baltic Sea were studied. (4) Chemical speciation of I-129. Seawater samples from in the North Sea, Kattegat and Baltic Sea were analyzed for 129 I and 127 I in both iodide and iodate species and total inorganic iodine. The possibility of using this method to study the geochemical cycle of iodine in the ocean was investigated. (author)

  13. Physico-Chemical Research on the Sounding Rocket Maser 13

    Science.gov (United States)

    Lockowandt, Christian; Kemi, Stig; Abrahamsson, Mattias; Florin, Gunnar

    instabilities. The model reaction is the autocatalytic iodate oxidation of arsenous acid, where surface tension changes due to the change in composition. The experiment will be performed by injecting the fluids into an experiment cell and the reaction will be triggered by an electrical pulse. The chemical reaction front and the dynamics of the liquid will be monitored by different optical systems. MEDI The general objective of the investigation is to improve the understanding of the physical phenomena that govern the formation of the columnar-to-equiaxed transition (CET) in alloy solidification and its consequences for casting soundness. In the frame of the experiment MEDI on MASER 13 the goal is to investigate the formation of an equiaxed microstructure under low gravity conditions.

  14. Adsorption and revaporisation studies of thin iodine oxide and CsI aerosol deposits from containment surface materials in LWRs

    Energy Technology Data Exchange (ETDEWEB)

    Tietze, S.; Foreman, M.; Ekberg, C. [Chalmers Univ. of Technology, Goeteborg (Sweden); Kaerkelae, T.; Auvinen, A.; Tapper, U.; Jokiniemi, J. [VTT Technical Research Centre of Finland, Espoo (Finland)

    2013-07-15

    speciation of the particles. The formation of HIO{sub 3} was verified with Raman analysis regardless of the reaction temperature. Furthermore, elemental iodine was also observed in the measured Raman spectra. Probably, iodine oxide particles had reacted with air humidity forming iodic acid and elemental iodine. IOx and CsI particles that were deposited on various sample surfaces were synthesized at 120 deg. C. According to XPS analysis, it seemed that IOx particles were mainly in form of HIO{sub 3} on the metal and on the painted surfaces. The XPS spectrum of CsI was observed on all metal and painted samples on which CsI particles were deposited. However, the CsI particles seemed to have dissolved at least partially by air humidity. Iodine was observed at areas outside the caesium iodide deposits on metal and on painted surfaces. According to the XPS analyses, iodine was in oxidised form. The measurements indicated that iodine may have reacted with the oxidized metal surfaces to form metal iodates. Only trace amounts of oxidized iodine were detected on the painted surfaces. An interesting result in the XPS analysis was that a part of the acquired signal from CsI on the painted surfaces seemed to originate deeper from the structure of the paint when it was pre-treated either with heat or gamma irradiation. SEM analysis revealed that heat and gamma irradiation treatment increased the porosity of the paint. Therefore, dissolved CsI may have been transported into the matrix of the paint. Besides copper the studied metal surfaces underwent slow reactions with the iodine of the aerosol deposits which showed in the high revaporisation rates at room temperature and elevated temperatures. On the copper and paint samples it could be shown that these surfaces react more easily with the iodine from cesium iodide deposits. From the chemically converted metal iodides only copper iodide remained on the surfaces after exposure to hot humid air and as well after immersion in boiling water

  15. Radio-active colloids in the functional exploration of the reticulo-endothelium system; Les colloides radioactifs dans l'exploration fonctionnelle du systeme reticulo-endothelial

    Energy Technology Data Exchange (ETDEWEB)

    Chivot, J.J. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1967-03-01

    A historical review describes the reticulo-endothelial system (R.E.S.) and aims at defining it and at explaining its operation. The methods used for its examination and the colloids utilized are considered. The author has been led to prepare a special type of colloid: an albuminous complex containing radio-iodine, 'C.A. {sup 131}I', whose method of preparation and physical and biological examination are described. A human albumin, having a known optical density in solution, is heated until a change in the optical density indicates that an aggregation of the proteinic molecules has occurred. The denatured protein is iodated with {sup 131}I. Electrophoretic, ultracentrifuge and autoradiographic controls are then carried out. This atoxic and metabolisable preparation of biological origin is compared with the better defined colloidal gold which serves as reference. C.A.{sup 131}I is injected into mice. It is shown by radioactivity measurements, auto-radiographies on sections of the whole animal, and anthropo-gamma-metric detections that a high concentration occurs in the S.R.E. of the liver. These static results are only of limited importance however compared to those obtained from an in vivo study of the phenomenon. The author records the changes in the radioactivity of the blood derived from the carotid artery using a well-scintillator. He obtains directly a curve of the radioactivity of blood having a decreasing exponential form; the mathematical expression describing this curve is given. The biological half-life T 1/2 of the colloid in the blood is a measure of its phagocytosis by the S.R.E. cells. A supplementary check is provided by the direct recording of the hepatic activity using a suitably collimated exterior detector. A curve of increasing-exponential form is obtained and its parameters are corollary to the preceding curve. These tests carried out on guinea-pigs and rats make it possible to give to the S.R.E. a phagocytic index which is