WorldWideScience

Sample records for chromium perchlorates

  1. Acute and chronic activity of perchlorate and hexavalent chromium contamination on the survival and development of Culex quinquefasciatus Say (Diptera: Culicidae)

    International Nuclear Information System (INIS)

    Effects of water contamination with perchlorate and hexavalent chromium [Cr (VI)] on the mosquito Culex quinquefasciatus were assessed. The chronic (10-day) LC5s values for perchlorate and chromium were 74 ± 8.0 mg/L and 0.41 ± 0.15 mg/L, respectively. Relative Growth Index, a measure of growth and mortality rates in a population, was significantly reduced within 5 days for levels of perchlorate as low as 25 mg/L and for levels of chromium as low as 0.16 mg/L. Neither compound altered wing length of surviving adults. In combination, contaminants were synergistic, causing 14% more mortality than predicted. Acute (24-h) LC5 values for perchlorate and Cr (VI) were 17,000 ± 3200 and 38 ± 1.3 mg/L, respectively. Effects on mosquito larvae in contaminated environments are likely to be observed for Cr (VI) but not for perchlorate, which generally does not occur at levels as high as those shown here to affect larval mosquitoes. - While pollution with hexavalent chromium may adversely affect Culex quinquefasciatus larvae, levels of perchlorate currently in the environment will not impact these insects

  2. Acute and chronic activity of perchlorate and hexavalent chromium contamination on the survival and development of Culex quinquefasciatus Say (Diptera: Culicidae)

    Energy Technology Data Exchange (ETDEWEB)

    Sorensen, Mary A. [Department of Entomology, University of California, Riverside, CA 92521 (United States)]. E-mail: mary.sorensen@email.ucr.edu; Jensen, Peter D. [Department of Entomology, University of California, Riverside, CA 92521 (United States); Walton, William E. [Department of Entomology, University of California, Riverside, CA 92521 (United States); Trumble, John T. [Department of Entomology, University of California, Riverside, CA 92521 (United States)

    2006-12-15

    Effects of water contamination with perchlorate and hexavalent chromium [Cr (VI)] on the mosquito Culex quinquefasciatus were assessed. The chronic (10-day) LC{sub 5}s values for perchlorate and chromium were 74 {+-} 8.0 mg/L and 0.41 {+-} 0.15 mg/L, respectively. Relative Growth Index, a measure of growth and mortality rates in a population, was significantly reduced within 5 days for levels of perchlorate as low as 25 mg/L and for levels of chromium as low as 0.16 mg/L. Neither compound altered wing length of surviving adults. In combination, contaminants were synergistic, causing 14% more mortality than predicted. Acute (24-h) LC{sub 5} values for perchlorate and Cr (VI) were 17,000 {+-} 3200 and 38 {+-} 1.3 mg/L, respectively. Effects on mosquito larvae in contaminated environments are likely to be observed for Cr (VI) but not for perchlorate, which generally does not occur at levels as high as those shown here to affect larval mosquitoes. - While pollution with hexavalent chromium may adversely affect Culex quinquefasciatus larvae, levels of perchlorate currently in the environment will not impact these insects.

  3. A novel hydrolysis method to synthesize chromium hydroxide nanoparticles and its catalytic effect in the thermal decomposition of ammonium perchlorate

    International Nuclear Information System (INIS)

    Highlights: ► Synthesis of Cr(OH)3 nanoparticles in Cr3+–F− aqueous solution. ► The F− ion tailors coagulated materials, Cr(OH)3 nanoparticles are obtained. ► Adding nanosized Cr(OH)3, AP thermal decomposition temperature decreases to 200 °C. ► The nanosized Cr(OH)3 catalyzes NH3 oxidation, accelerating AP thermal decomposition. - Abstract: A procedure for the preparation of spherical Cr(OH)3 nanoparticles was developed based on the aging of chromium nitrate aqueous solutions in the presence of sodium fluoride, urea, and polyvinylpyrrolidone. Using scanning electron microscopy, transmission electron microscopy, and energy dispersive spectroscopy, the morphological characteristics of Cr(OH)3 were controlled by altering the molar ratio of fluoride ion to chromium ion, as well as the initial pH and chromium ion concentration. The prepared nanosized Cr(OH)3 decreased the temperature required to decompose ammonium perchlorate from 450 °C to about 250 °C as the catalyst. The possible catalytic mechanism of the thermal decomposition of ammonium perchlorate was also discussed.

  4. Chromium

    Science.gov (United States)

    ... health risks of too much chromium? Chromium and medication interactions Supplemental sources of chromium Chromium and Healthful Diets References Disclaimer What foods provide chromium? Chromium is widely distributed in the ...

  5. cis-Difluoridobis(1,10-phenanthroline)chromium(III) perchlorate monohydrate

    DEFF Research Database (Denmark)

    Birk, Torben; Bendix, Jesper; Weihe, Högni

    2008-01-01

    The title complex, [CrF(2)(C(12)H(8)N(2))(2)]ClO(4)·H(2)O, displays a slightly distorted octa-hedral coordination geometry around the central chromium(III) ion. The Cr environment is composed of a cis arrangement of two 1,10-phenanthroline [average Cr(III)-N = 2.0726 (10) Å] and two fluoride...... [average Cr(III)-F = 1.8533 (6) Å] ligands. The water molecule forms a hydrogen bond to fluorine in a neighbouring cation....

  6. Crystal structure of trans-bis(ethane-1,2-diamine-κ2N,N′)bis(thiocyanato-κN)chromium(III) perchlorate from synchrotron data

    OpenAIRE

    Dohyun Moon; Jong-Ha Choi

    2015-01-01

    The structure of the title compound, [Cr(NCS)2(C2H8N2)2]ClO4, has been determined from synchroton data. The asymmetric unit consists of one half of a centrosymmetric CrIII complex cation and half of a perchlorate anion with the Cl atom on a twofold rotation axis. The CrIII ion is coordinated by the four N atoms of two ethane-1,2-diamine (en) ligands in the equatorial plane and two N-bound thiocyanate (NCS−) anions in a trans-axial arrangement, displaying a slightly distorted octahedral geomet...

  7. Solvent extraction of seven trivalent metal ions in aqueous perchlorate solutions with trioctylphosphine oxide in hexane and rapid extraction of chromium(III)

    International Nuclear Information System (INIS)

    Solvent extraction of scandium(III), yttrium(III), lanthanum(III), europium(III), gallium(III), indium(III), and chromium(III) in weakly acidified 1 mol dm-3 NaClO4 solutions with trioctylphosphine oxide (TOPO) in hexane was studied. The extraction equilibrium was established by the two phase agitation for within 3 min and the extracted species except chromium(III) were found to be M(TOPO)43+(ClO4-)3. The extraction of chromium(III) was also achieved by the two phase agitation for only a short time but, from the dependence of the extraction on the TOPO concentration, the extracted species was assumed to be Cr(TOPO)63+(ClO4-)3. Since the inert Cr(H2O)63+ was so rapidly extracted and the solvation number was higher than that of the other metal ions, the TOPO molecules were assumed to combine with the hydrating water molecules by hydrogen bonds which can be formed in a short time even when the metal ion was inert. The chromium(III) was also extracted rapidly from 1 mol dm-3 NaSCN, NaNO3, NaBr, and NaCl solutions with TOPO in hexane and the extraction was better from NaSCN solution than from NaClO4 solution but it was not effective from the solutions of other salts. (author)

  8. Perchlorate in seawater

    Energy Technology Data Exchange (ETDEWEB)

    Martinelango, P. Kalyani [Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, TX 79409-1061 (United States); Tian Kang [Institute of Environmental and Human Health, Texas Tech University, Lubbock, TX 79409 (United States); Dasgupta, Purnendu K. [Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, TX 79409-1061 (United States)]. E-mail: Sandyd@ttu.edu

    2006-05-10

    There has been no reliable published data on the presence of perchlorate in seawater. Seaweeds are among the most important plant life in the ocean and are good sources of iodine and have been widely used as food and nutritional supplement. Perchlorate is known to inhibit the transport of iodide by the sodium iodide symporter (NIS), present e.g., in the thyroid and mammary glands. With perchlorate being increasingly detected in drinking water, milk and various other foods, increasing the iodide intake through inexpensive natural supplements may be an attractive solution for maintaining iodine assimilation. We report here measurable concentrations of perchlorate in several samples of seawater (detectable in about half the samples analyzed). We also report the iodide and perchlorate concentrations of 11 different species of seaweed and the corresponding bioconcentration factors (BCF) for perchlorate and iodide, relative to the seawater from which they were harvested. All seaweed samples came from the same region, off the coast of Northeastern Maine. Concentrations of iodide and perchlorate in four seawater samples collected from the region near harvest time were 30 {+-} 11 and 0.16 {+-} 0.084 {mu}g l{sup -1}, respectively. Concentrations of both iodide and perchlorate varied over a wide range for different seaweed species; iodide ranging from 16 to 3134 mg kg{sup -1} and perchlorate from 0.077 to 3.2 mg kg{sup -1}. The Laminaria species had the highest iodide concentration; Laminaria digitata is the seaweed species most commonly used in the kelp tablets sold in health food stores. Our sample of L. digitata contained 3134 {+-} 15 mg iodide/kg dry weight. The BCF varied widely for different species, with Laminaria species concentrating iodide preferentially over perchlorate. The iodide BCF (BCF{sub i}) to perchlorate BCF (BCF{sub p}) quotient ranged from 0.66 to 53; L. digitata and L. saccarina having a BCF{sub i}/BCF{sub p} value of 45 and 53, respectively, far

  9. Breastfed infants metabolize perchlorate.

    Science.gov (United States)

    Shelor, C Phillip; Kirk, Andrea B; Dasgupta, Purnendu K; Kroll, Martina; Campbell, Catrina A; Choudhary, Pankaj K

    2012-05-01

    Bifidobacteria are the dominant intestinal bacteria in breastfed infants. It is known that they can reduce nitrate. Although no direct experiments have been conducted until now, inferred pathways for Bifidobacterium bifidum include perchlorate reduction via perchlorate reductase. We show that when commercially available strains of bifidobacteria are cultured in milk, spiked with perchlorate, perchlorate is consumed. We studied 13 breastfed infant-mother pairs who provided 43 milk samples and 39 infant urine samples, and 5 formula-fed infant-mother pairs who provided 21 formula samples and 21 infant urine samples. Using iodine as a conservative tracer, we determined the average urinary iodine (UI) to milk iodine (MI) concentration ratio to be 2.87 for the breastfed infants. For the same samples, the corresponding perchlorate concentration ratio was 1.37 (difference significant, p perchlorate is lost. For the formula fed infant group the same ratios were 1.20 and 1.58; the difference was not significant (p = 0.68). However, the small number of subjects in the latter group makes it more difficult to conclude definitively whether perchlorate reduction does or does not occur. PMID:22497505

  10. Bioelectrical Perchlorate Remediation

    Science.gov (United States)

    Thrash, C.; Achenbach, L. A.; Coates, J. D.

    2007-12-01

    Several bioreactor designs are currently available for the ex-situ biological attenuation of perchlorate- contaminated waters and recently, some of these reactor designs were conditionally approved by the California Department of Health Services for application in the treatment of perchlorate contaminated drinking water. However, all of these systems are dependent on the continual addition of a chemical electron donor to sustain microbial activity and are always subject to biofouling and downstream water quality issues. In addition, residual labile electron donor in the reactor effluent can stimulate microbial growth in water distribution systems and contribute to the formation of potentially toxic trihalomethanes during disinfection by chlorination. As part of our ongoing studies into microbial perchlorate reduction we investigated the ability of dissimilatory perchlorate reducing bacteria (DPRB) to metabolize perchlorate using a negatively charged electrode (cathode) in the working chamber of a bioelectrical reactor (BER) as the primary electron donor. In this instance the DPRB use the electrons on the electrode surface either directly or indirectly in the form of electrolytically produced H2 as a source of reducing equivalents for nitrate and perchlorate reduction. As part of this investigation our fed-batch studies showed that DPRB could use electrons from a graphite cathode poised at -500mV (vs. Ag/AgCl) for the reduction of perchlorate and nitrate. We isolated a novel organism, Dechlorospirillum strain VDY, from the cathode surface after 70 days operation which readily reduced 100 mg.L-1 perchlorate in a mediatorless batch bioelectrical reactor (BER) in 6 days. Continuous up-flow BERs (UFBERs) seeded with active cultures of strain VDY continuously treated waters containing 100 mg.L-1 perchlorate with almost 100% efficiency throughout their operation achieving a non-optimized volumetric loading of 60 mg.L-1 reactor volume.day-1. The same UFBERs also treated

  11. Evaluation of chromium concentration in cattle feces using different acid digestion and spectrophotometric quantification techniques

    OpenAIRE

    N.K.P. Souza; E. Detmann; D. S. Pina; Valadares Filho, S. C.; C.B. Sampaio; A.C. Queiroz; C.M. Veloso

    2013-01-01

    The objective of this work was to evaluate combinations between acid digestion techniques and spectrophotometric quantification to measure chromium concentration in cattle feces. Digestion techniques were evaluated based on the use of nitric and perchloric acids, sulfuric and perchloric acids, and phosphoric acid. The chromium quantification in the solutions was performed by colorimetry and by atomic absorption spectrophotometry (AAS). When AAS was used, the addition of calcium chloride to th...

  12. Isotopic mapping of groundwater perchlorate plumes.

    Science.gov (United States)

    Sturchio, Neil C; Hoaglund, John R; Marroquin, Roy J; Beloso, Abelardo D; Heraty, Linnea J; Bortz, Sarah E; Patterson, Thomas L

    2012-01-01

    Analyses of stable isotope ratios of chlorine and oxygen in perchlorate can, in some cases, be used for mapping and source identification of groundwater perchlorate plumes. This is demonstrated here for large, intersecting perchlorate plumes in groundwater from a region having extensive groundwater perchlorate contamination and a large population dependent on groundwater resources. The region contains both synthetic perchlorate derived from rocket fuel manufacturing and testing activities and agricultural perchlorate derived predominantly from imported Chilean (Atacama) nitrate fertilizer, along with a likely component of indigenous natural background perchlorate from local wet and dry atmospheric deposition. Most samples within each plume reflect either a predominantly synthetic or a predominantly agricultural perchlorate source and there is apparently a minor contribution from the indigenous natural background perchlorate. The existence of isotopically distinct perchlorate plumes in this area is consistent with other lines of evidence, including groundwater levels and flow paths as well as the historical land use and areal distribution of potential perchlorate sources. PMID:21352209

  13. 2-(Benzenesulfonamidopyridinium perchlorate

    Directory of Open Access Journals (Sweden)

    Xun Li

    2009-06-01

    Full Text Available In the title compound, C11H11N2O2S+·ClO4−, the dihedral angle between the benzene and pyridinium rings is 87.33 (10°. An intramolecular N—H...O interaction, with an S=O-bonded O atom as receptor, occurs in the cation. In the crystal structure, ion pairs occur, being linked by strong N—H...O hydrogen bonds. The perchlorate anion plays a further role in the molecular packing by accepting several weak C—H...O interactions.

  14. Method of trivalent chromium concentration determination by atomic spectrometry

    Science.gov (United States)

    Reheulishvili, Aleksandre N.; Tsibakhashvili, Neli Ya.

    2006-12-12

    A method is disclosed for determining the concentration of trivalent chromium Cr(III) in a sample. The addition of perchloric acid has been found to increase the atomic chromium spectrometric signal due to Cr(III), while leaving the signal due to hexavalent chromium Cr(VI) unchanged. This enables determination of the Cr(III) concentration without pre-concentration or pre-separation from chromium of other valences. The Cr(III) concentration may be measured using atomic absorption spectrometry, atomic emission spectrometry or atomic fluorescence spectrometry.

  15. USE OF TWO DIGESTION METHODS IN THE EVALUATION OF CHROMIUM CONTENT IN CATTLE'S MEAT SUPPLEMENTED WITH CHROMIUM CHELATES

    OpenAIRE

    R. L. T. Andrade; P.S.A. Moreira; R. Arruda; F. J. Lourenço; C. Palhari, F. F. Faria, V. B. Arevalo; Faria, F. F.; V. B. Arevalo

    2015-01-01

    The present study aimed to analyze the chromium content in beef using two digestion methods. There were used samples from 24 18-month-old male cattle, and twelve of them were supplemented and twelve were not supplemented with chromium chelate. These samples were evaluated by atomic absorption spectroscopy, previously submitted to digestion method using nitric acid (65%) with hydrogen peroxide (35%) and to digestion method, using solution of nitric perchloric acid in the proportion 3:1. Immedi...

  16. Effect of nitrate on microbial perchlorate reduction

    Science.gov (United States)

    Sun, Y.; Coates, J. D.

    2007-12-01

    Over the last decade perchlorate has been recognized as an important emerging water contaminant that poses a significant public health threat. Because of its chemical stability, low ionic charge density, and significant water solubility microbial remediation has been identified as the most feasible method for its in situ attenuation. Our previous studies have demonstrated that dissimilatory perchlorate reducing bacteria (DPRB) capable of the respiratory reduction of perchlorate into innocuous chloride are ubiquitous in soil and sedimentary environments. As part of their metabolism these organisms reduce perchlorate to chlorite which is subsequently dismutated into chloride and molecular oxygen. These initial steps are mediated by the perchlorate reductase and chlorite dismutase enzymes respectively. Previously we found that the activity of these organisms is dependent on the presence of molybdenum and is inhibited by the presence of oxygen and to different extents nitrate. However, to date, there is little understanding of the mechanisms involved in the regulation of perchlorate reduction by oxygen and nitrate. As a continuation of our studies into the factors that control DPRB activity we investigated these regulatory mechanisms in more detail as a model organism, Dechloromonas aromatica strain RCB, transitions from aerobic metabolism through nitrate reduction to perchlorate reduction. In series of growth transition studies where both nitrate and perchlorate were present, preference for nitrate to perchlorate was observed regardless of the nitrate to perchlorate ratio. Even when the organism was pre-grown anaerobically in perchlorate, nitrate was reduced prior to perchlorate. Using non-growth washed cell suspension, perchlorate- grown D. aromatica was capable of reducing both perchlorate and nitrate concomitantly suggesting the preferentially utilization of nitrate was not a result of enzyme functionality. To elucidate the mechanism for preferential utilization of

  17. Peptide biomarkers as evidence of perchlorate biodegradation.

    Science.gov (United States)

    Bansal, Reema; Crawford, Ronald L; Paszczynski, Andrzej J

    2011-02-01

    Perchlorate is a known health hazard for humans, fish, and other species. Therefore, it is important to assess the response of an ecosystem exposed to perchlorate contamination. The data reported here show that a liquid chromatography-mass spectrometry-based proteomics approach for the detection of perchlorate-reducing enzymes can be used to measure the ability of microorganisms to degrade perchlorate, including determining the current perchlorate degradation status. Signature peptides derived from chlorite dismutase (CD) and perchlorate reductase can be used as biomarkers of perchlorate presence and biodegradation. Four peptides each derived from CD and perchlorate reductase subunit A (PcrA) and seven peptides derived from perchlorate reductase subunit B (PcrB) were identified as signature biomarkers for perchlorate degradation, as these sequences are conserved in the majority of the pure and mixed perchlorate-degrading microbial cultures examined. However, chlorite dismutase signature biomarker peptides from Dechloromonas agitata CKB were found to be different from those in other cultures used and should also be included with selected CD biomarkers. The combination of these peptides derived from the two enzymes represents a promising perchlorate presence/biodegradation biomarker system. The biomarker peptides were detected at perchlorate concentrations as low as 0.1 mM and at different time points both in pure cultures and within perchlorate-reducing environmental enrichment consortia. The peptide biomarkers were also detected in the simultaneous presence of perchlorate and an alternate electron acceptor, nitrate. We believe that this technique can be useful for monitoring bioremediation processes for other anthropogenic environmental contaminants with known metabolic pathways. PMID:21115710

  18. Organic carbon biostimulates rapid rhizodegradation of perchlorate.

    Science.gov (United States)

    Yifru, Dawit D; Nzengung, Valentine A

    2008-12-01

    Previous hydroponics and field studies identified phytodegradation and rhizodegradation as the two main mechanisms by which plants metabolize perchlorate. Plant uptake and phytodegradation of perchlorate is a slower and undesired process that poses ecological risks resulting from phytoaccumulation of some fraction of the perchlorate. Meanwhile, rhizodegradation is a more rapid and favored process involving perchlorate-degrading bacteria utilizing dissolved organic carbon (DOC) as a carbon and energy (electron) source to rapidly degrade perchlorate to innocuous chloride. In the present study, rhizodegradation of perchlorate by willow trees (Salix nigra) was biostimulated using electron sources obtained from natural and artificial carbon sources. In bioreactors provided with carbon sources as 500 mg/L DOC, 25 to 40 mg/L of initial perchlorate concentrations were removed to below the ion chromatography method detection limit of 2 microg/L in approximately 9 d. For planted controls provided with no electron donors, the time required for the complete removal of the same doses of perchlorate was up to 70 d. Enhancement of rhizodegradation by organic carbon reduced the phytoaccumulated fraction of perchlorate by an order of magnitude from approximately 430 to 20 mg/kg. The implication of the present study is that the high fraction uptake and phytoaccumulation of perchlorate in agricultural products and the recycling of perchlorate into the ecosystem can be significantly curtailed by supplying electron donors derived from organic carbon sources to the root zone of plants. PMID:18593217

  19. Perchlorate Removal in groundwater by perchlorate reductases from the perchlorate respiring bacterium, perc1ace

    OpenAIRE

    Frankenberger, William

    2003-01-01

    [Note: See PDF for correct symbols.] Perchlorate (ClO4-) is an important energetic component of solid rocket fuel. The major source of ClO4- pollution is the military, space program and supporting industries. ClO4- is recalcitrant in the environment and is potentially toxic. The California Department of Health Services adopted an action level of 4 ppb for perchlorate in potable water. Microorganisms that reduce ClO4- to chloride and molecular oxygen have been isolated. For designing an effici...

  20. PERCHLORATE PHYTOREMEDIATION USING HARDWOOD TREES AND VASCULAR PLANTS

    Science.gov (United States)

    Perchlorate has contaminated water and soils at several locations in the United States. Perchlorate iswater soluble, exceedingly mobile in aqueous systems, and can persist for many decades under typical ground and surface water conditions. Perchlorate is of concern because of...

  1. PHYTOREMEDIATION OF PERCHLORATE BY TOBACCO PLANTS

    Science.gov (United States)

    Previous studies have shown that tobacco plants are tolerant of perchlorate and will accumulate perchlorate in the plant tissues. The objective of this research was to determine the effectiveness of tobacco plants in phytoremediation, a technology that employs plants to degrade,...

  2. Peptide Biomarkers as Evidence of Perchlorate Biodegradation▿ †

    OpenAIRE

    Bansal, Reema; Crawford, Ronald L.; Paszczynski, Andrzej J.

    2010-01-01

    Perchlorate is a known health hazard for humans, fish, and other species. Therefore, it is important to assess the response of an ecosystem exposed to perchlorate contamination. The data reported here show that a liquid chromatography-mass spectrometry-based proteomics approach for the detection of perchlorate-reducing enzymes can be used to measure the ability of microorganisms to degrade perchlorate, including determining the current perchlorate degradation status. Signature peptides derive...

  3. Perchlorate reduction by microbes inhabiting oil reservoirs

    Science.gov (United States)

    Liebensteiner, Martin; Stams, Alfons; Lomans, Bart

    2014-05-01

    Microbial perchlorate and chlorate reduction is a unique type of anaerobic respiration as during reduction of (per)chlorate chlorite is formed, which is then split into chloride and molecular oxygen. In recent years it was demonstrated that (per)chlorate-reducing bacteria may employ oxygenase-dependent pathways for the degradation of aromatic and aliphatic hydrocarbons. These findings suggested that (per)chlorate may be used as oxygen-releasing compound in anoxic environments that contain hydrocarbons, such as polluted soil sites and oil reservoirs. We started to study perchlorate reduction by microbes possibly inhabiting oil reservoirs. One of the organisms studied was Archaeoglobus fulgidus. This extremely thermophilic archaeon is known as a major contributor to souring in hot oil reservoirs. A. fulgidus turned out to be able to use perchlorate as terminal electron acceptor for growth with lactate (Liebensteiner et al 2013). Genome based physiological experiments indicated that A. fulgidus possesses a novel perchlorate reduction pathway. Perchlorate is first reduced to chlorite, but chlorite is not split into chloride and molecular oxygen as occurs in bacteria. Rather, chlorite reacts chemically with sulfide, forming oxidized sulfur compounds, which are reduced to sulfide in the electron transport chain by the archaeon. The dependence of perchlorate reduction on sulfur compounds could be shown. The implications of our findings as novel strategy for microbiological enhanced oil recovery and for souring mitigation are discussed. Liebensteiner MG, Pinkse MWH, Schaap PJ, Stams AJM and Lomans BP (2013) Archaeal (per)chlorate reduction at high temperature, a matter of abiotic-biotic reactions. Science 340: 85-87

  4. Evaluation of chromium concentration in cattle feces using different acid digestion and spectrophotometric quantification techniques

    Directory of Open Access Journals (Sweden)

    N.K.P. Souza

    2013-10-01

    Full Text Available The objective of this work was to evaluate combinations between acid digestion techniques and spectrophotometric quantification to measure chromium concentration in cattle feces. Digestion techniques were evaluated based on the use of nitric and perchloric acids, sulfuric and perchloric acids, and phosphoric acid. The chromium quantification in the solutions was performed by colorimetry and by atomic absorption spectrophotometry (AAS. When AAS was used, the addition of calcium chloride to the solutions as a releasing agent was also evaluated. Several standard samples containing known chromium contents were produced (0, 2, 4, 6, 8 and 10g of chromium per kg of feces using cattle feces obtained from three different animals to evaluate the accuracy of the different combinations of techniques. The accuracy was evaluated by adjusting a simple linear regression model of the estimated values on the actual values of chromium content in the standard samples. Regardless of the digestion technique, the chromium content estimates in the standard samples obtained by colorimetry were not accurate (P0.05. The use of the digestion technique in phosphoric acid provided incomplete recovery of the fecal chromium (P0.05 fecal chromium contents.

  5. A Colorimetric Bioassay for Perchlorate

    Science.gov (United States)

    Heinnickel, M. L.; Smith, S.; Coates, J. D.

    2007-12-01

    Recognition of perchlorate (ClO4-) as a widespread contaminant across the United States and its potential adverse affects towards human health has motivated the EPA to place ClO4- on its contaminant candidate list for drinking water supplies. While a federal MCL has not yet been set, a recommended public health goal of 1 ppb (μg.L-1) was established by the US EPA in 2002. To date, methods of detection require use of sensitive ion chromatographic equipment that are expensive, time consuming, and require highly trained personnel for use. Our studies are focused on the development of a highly sensitive, simple, and robust colorimetric bioassay based on the primary enzyme involved in microbial ClO4- reduction, the perchlorate reductase (Pcr). A previously published assay used reduced methyl viologen (MV, the dye is reduced with sodium hydrosulfite) as an electron donor to demonstrate Pcr activity. The assay directly correlates the amount of MV oxidized with the amount of ClO4- reduced by assuming a transfer of four electrons. To test this assumption, we compared actual concentrations of MV oxidized to ClO4- reduced in this assay. ClO4- concentrations were determined using a Dionex ICS-500 ion chromatography system, while MV concentrations were determined using a standard curve generated at 578 nm. Comparisons between the two revealed that twelve molecules of MV were oxidized for each molecule of ClO4- reduced. The oxidation of these additional eight MV molecules is explained by the interaction of the dye with chlorite (the product of the Pcr reaction) and other contaminants that could be present in the enzyme prep. This unsettling result indicated this assay would be problematic for the detection of ClO4- in soil, which has many chemicals that could react with MV. To improve upon this assay, we have tried to reduce ClO4- using less reactive dyes and reductants. The reductants ascorbic acid, NADH, and dithiothreitol drive Pcr catalyzed ClO4- reduction, however, they

  6. The Microbiology of Perchlorate in the Environment

    Science.gov (United States)

    Coates, J. D.

    2007-12-01

    In the last decade perchlorate has been identified as an important groundwater component that poses potential health threat. Although primarily sourced anthropogenically, many recent studies have identified significant natural pools throughout the US and the natural mechanisms of its synthesis remain a mystery. As such, the true perchlorate concentrations naturally present in the environment are still unknown making its regulation problematic. Because of its solubility and non-reactivity the fate and transport of perchlorate in the environment is primarily a function of microbial activity. In the last seven years more than forty specialized perchlorate respiring organisms have been identified and characterized. These dissimilatory perchlorate reducing bacteria (DPRB) are metabolically diverse and environmental populations tend to be dominated by two primary genotypes, the Dechloromonas and the Azospira species. As such, the majority of our understanding of this metabolism is based on these organisms. These organisms are readily found in soil and sedimentary environments and often associate with the rhizosphere. Recent research has demonstrated an accumulation of these organisms along plant roots suggesting their catabolism of root exudates and molecular studies has demonstrated their existence as endophytic infections of the stem and leaves of actively growing Brachypodium grass plants although their exact role under these conditions is unknown. These microorganisms are generally not nutritionally fastidious and vitamin supplementation is unnecessary for growth although molybdenum is a required trace element for perchlorate reduction. The Dechloromonas and Azospira species generally grow optimally at pH values near neutrality in freshwater environments. Even so, recent field studies have shown that related deep-branching members of these genera often predominate in sites of adverse pH or salinity with some species being capable of growth and perchlorate respiration

  7. Silver(I) imidazole perchlorate

    International Nuclear Information System (INIS)

    The crystal structure of silver(I) imidazole perchlorate reveals the presence of a planar (Ag+)6 cluster, in which three radiating pairs of Ag+ ions 3.051(1) A apart are disposed on the corners of an equilateral triangle, the inner Ag+ ions being 3.493(1) A apart. Each silver ion carries two linearly co-ordinated imidazole ligands, the whole unit has 32 (D3) symmetry. Exposure to 60Co γ-rays at 77 K results in electron addition to a group of three equivalent silver atoms. The 109Ag, 107Ag, and 14N hyperfine coupling constants show that the total 5s character of the unpaired electron is only ca. 0.55, and delocalisation onto six equivalent nitrogen ligands accounts for ca. 0.25. Low g values suggest that the remaining spin density is in 5p orbitals on silver. There is no indication of delocalisation onto the remaining three Ag+ ions in the cluster. Possible reasons for this selectivity are discussed. The electron-loss centre appears to be a normal Ag2+ complex. It is suggested that marked distortion results in the hole being trapped on one silver rather than being delocalised. (author)

  8. Perchlorate in The Great Lakes: Isotopic Composition and Origin

    OpenAIRE

    Poghosyan, Armen; Sturchio, Neil C.; Morrison, Candice G.; Beloso, Abelardo D., Jr.; Guan, Yunbin; Eiler, John M.; Jackson, W. Andrew; Hatzinger, Paul B.

    2014-01-01

    Perchlorate is a persistent and mobile contaminant in the environment with both natural and anthropogenic sources. Stable isotope ratios of oxygen (δ^(18)O, Δ^(17)O) and chlorine (δ^(37)Cl) along with the abundance of the radioactive isotope ^(36)Cl were used to trace perchlorate sources and behavior in the Laurentian Great Lakes. These lakes were selected for study as a likely repository of recent atmospheric perchlorate deposition. Perchlorate concentrations in the Great Lakes range from 0....

  9. Identification, Characterization, and Classification of Genes Encoding Perchlorate Reductase

    OpenAIRE

    Bender, Kelly S.; Shang, Ching; Chakraborty, Romy; Belchik, Sara M.; Coates, John D.; Achenbach, Laurie A.

    2005-01-01

    The reduction of perchlorate to chlorite, the first enzymatic step in the bacterial reduction of perchlorate, is catalyzed by perchlorate reductase. The genes encoding perchlorate reductase (pcrABCD) in two Dechloromonas species were characterized. Sequence analysis of the pcrAB gene products revealed similarity to α- and β-subunits of microbial nitrate reductase, selenate reductase, dimethyl sulfide dehydrogenase, ethylbenzene dehydrogenase, and chlorate reductase, all of which are type II m...

  10. Environmental biotechnology and microbiology of (per)chlorate reducing bacteria

    NARCIS (Netherlands)

    Mehboob, F.; Schraa, G.; Stams, A.J.M.

    2011-01-01

    Perchlorates are the salts derived from perchloric acid (HClO4). They occur both naturally and through manufacturing. They have been used as a medicine for more than 50 years to treat thyroid gland disorders and are used extensively within the pyrotechnics industry, and ammonium perchlorate is also

  11. Heterogeneous chromium catalysts

    OpenAIRE

    2005-01-01

    The present invention relates to a heterogeneous chromium catalyst system for the polymerisation of ethylene and/or alpha olefins prepared by the steps of: (a) providing a silica-containing support, (b) treating the silica-containing support with a chromium compound to form a chromium-based silica-containing support, (c) activating the chromium-based silica-containing support, (d) chemically reducing the activated chromium-based silica-containing support to produce a precursor catalyst, (e) r...

  12. Quantitative Detection of Perchlorate-Reducing Bacteria by Real-Time PCR Targeting the Perchlorate Reductase Gene▿

    OpenAIRE

    Nozawa-Inoue, Mamie; Jien, Mercy; Hamilton, Nicholas S.; Stewart, Valley; Scow, Kate M.; Hristova, Krassimira R.

    2008-01-01

    A quantitative real-time PCR assay targeting the pcrA gene, encoding the catalytic subunit of perchlorate reductase, detected pcrA genes from perchlorate-reducing bacteria in three different genera and from soil microbial communities. Partial pcrA sequences indicated differences in the composition of perchlorate-reducing bacterial communities following exposure to different electron donors.

  13. Quantitative detection of perchlorate-reducing bacteria by real-time PCR targeting the perchlorate reductase gene.

    Science.gov (United States)

    Nozawa-Inoue, Mamie; Jien, Mercy; Hamilton, Nicholas S; Stewart, Valley; Scow, Kate M; Hristova, Krassimira R

    2008-03-01

    A quantitative real-time PCR assay targeting the pcrA gene, encoding the catalytic subunit of perchlorate reductase, detected pcrA genes from perchlorate-reducing bacteria in three different genera and from soil microbial communities. Partial pcrA sequences indicated differences in the composition of perchlorate-reducing bacterial communities following exposure to different electron donors. PMID:18245250

  14. Perchlorate levels in soil and waters from the Atacama Desert.

    Science.gov (United States)

    Calderón, R; Palma, P; Parker, D; Molina, M; Godoy, F A; Escudey, M

    2014-02-01

    Perchlorate is an anion that originates as a contaminant in ground and surface waters. The presence of perchlorate in soil and water samples from northern Chile (Atacama Desert) was investigated by ion chromatography-electrospray mass spectrometry. Results indicated that perchlorate was found in five of seven soils (cultivated and uncultivated) ranging from 290 ± 1 to 2,565 ± 2 μg/kg. The greatest concentration of perchlorate was detected in Humberstone soil (2,565 ± 2 μg/kg) associated with nitrate deposits. Perchlorate levels in Chilean soils are greater than those reported for uncultivated soils in the United States. Perchlorate was also found in superficial running water ranging from 744 ± 0.01 to 1,480 ± 0.02 μg/L. Perchlorate water concentration is 30-60 times greater than levels established by the United States Environmental Protection Agency (24.5 μg/L) for drinking. PMID:24165784

  15. Hexavalent Chromium Workshop

    Science.gov (United States)

    EPA is developing an updated IRIS assessment of hexavalent chromium. This assessment will evaluate the potential health effects of hexavalent chromium from oral and inhalation exposures. An important component of determining the cancer causing potential of ingested hexavalent chr...

  16. Atmospheric origins of perchlorate on Mars and in the Atacama

    Science.gov (United States)

    Catling, D. C.; Claire, M. W.; Zahnle, K. J.; Quinn, R. C.; Clark, B. C.; Hecht, M. H.; Kounaves, S.

    2010-01-01

    Isotopic studies indicate that natural perchlorate is produced on Earth in arid environments by the oxidation of chlorine species through pathways involving ozone or its photochemical products. With this analogy, we propose that the arid environment on Mars may have given rise to perchlorate through the action of atmospheric oxidants. A variety of hypothetical pathways can be proposed including photochemical reactions, electrostatic discharge, and gas-solid reactions. Because perchlorate-rich deposits in the Atacama desert are closest in abundance to perchlorate measured at NASA's Phoenix Lander site, we made a preliminary study of the means to produce Atacama perchlorate to help shed light on the origin of Martian perchlorate. We investigated gas phase pathways using a 1-D photochemical model. We found that perchlorate can be produced in sufficient quantities to explain the abundance of perchlorate in the Atacama from a proposed gas phase oxidation of chlorine volatiles to perchloric acid. The feasibility of gas phase production for the Atacama provides justification for future investigations of gas phase photochemistry as a possible source for Martian perchlorate.

  17. Plant-mediated transformation of perchlorate into chloride

    Energy Technology Data Exchange (ETDEWEB)

    Nzengung, V.A.; Wang, C. [Univ. of Georgia, Athens, GA (United States). Dept. of Geology; Harvey, G. [AEM, Wright Patterson AFB, OH (United States)

    1999-05-01

    The decontamination of perchlorate-contaminated water by woody plants was investigated in sand and hydroponic bioreactors. Willow trees were found to be the most favorable woody plants with phraetophytic characteristics in comparative screen tests with eastern cottonwoods and Eucalyptus cineria. Willows decontaminated aqueous solutions dosed with 10--100 mg/.L of perchlorate to below the method detection limit of 2 {micro}g/L. Two phytoprocesses were identified as important in the remediation of perchlorate-contaminated water: (1) uptake and phytodegradation of perchlorate in the tree branches and leaves and (2) rhizodegradation. Exposure of rooted willow trees to perchlorate-dosed media stimulated rhizodegradation. Homogeneous degradation studies using media from the root zone of dosed willow trees confirmed that rhizosphere-associated microorganisms mediated the degradation of perchlorate to chloride. Experiments conducted with varying ranges of nitrate concentrations clearly indicated that high nitrate concentrations interfered with rhizodegradation of perchlorate. This study provides evidence that the efficacy of phytoremediation of perchlorate-contaminated environments may depend on the concentration of competing terminal electron acceptors, such as nitrate, and the nitrogen source of the nutrient solution., Since perchlorate does not volatilize from water readily, a perchlorate remediation scheme may involve an intensively cultivated plantation of trees with phraetophytic characteristics and irrigation with the contaminated water.

  18. Chromium and Genomic Stability

    OpenAIRE

    Wise, Sandra S.; Wise, John Pierce

    2011-01-01

    Many metals serve as micronutrients which protect against genomic instability. Chromium is most abundant in its trivalent and hexavalent forms. Trivalent chromium has historically been considered an essential element, though recent data indicate that while it can have pharmacological effects and value, it is not essential. There are no data indicating that trivalent chromium promotes genomic stability and, instead may promote genomic instability. Hexavalent chromium is widely accepted as high...

  19. Perchlorate Exposure and Thyroid Function in Ammonium Perchlorate Workers in Yicheng, China

    Directory of Open Access Journals (Sweden)

    Hongxia Chen

    2014-05-01

    Full Text Available The impact of low level dust on the thyroid function of workers chronically exposed to ammonium perchlorate (AP is uncertain and controversial. The aim of this study was to examine whether workers in China with long-term (>3 years occupational exposure to low levels of AP dust had affected thyroid homeostasis. Mean occupational exposures to AP dust ranged from 0.43 to 1.17 mg/m3. Geometric means of post-shift urinary perchlorate levels were 20.5 µg/L for those exposed and 12.8 µg/L for the controls. No significant differences were found for thyroid function parameters of FT3, FT4, or log TSH or for TPO prevalence or thyroglobulin levels. Additionally, no differences in findings were observed for complete blood count (CBC, serum biochemical profile, or pulmonary function test. Median urinary iodine levels of 172 and 184 µg/L showed that the workers had sufficient iodine intake. This study found no effect on thyroid function from long term, low-level documented exposure to ammonium perchlorate. It is the first study to report both thyroid status parameters and urinary perchlorate, a biomarker of internal perchlorate exposure, in occupationally exposed workers in China.

  20. ACCUMULATION OF PERCHLORATE IN TOBACCO PLANTS: DEVELOPMENT OF A PLANT KINETIC MODEL

    Science.gov (United States)

    Previous studies have shown that tobacco plants are tolerant of perchlorate and will accumulate perchlorate in plant tissues. This research determined the uptake, translocation, and accumulation of perchlorate in tobacco plants. Three hydroponics growth studies were completed u...

  1. Different Strategies for Biological Remediation of Perchlorate Contaminated Groundwater

    OpenAIRE

    Wang, Yue

    2012-01-01

    Perchlorate (ClO4-) has gained attention recently due to its interference with thyroid gland function. In infants and unborn children, inadequate thyroid hormone production can cause mental retardation and thyroid tumors. Since new perchlorate standards will be proposed in 2013, and if a stricter standard is imposed, cost effective technologies will be in high demand. The overall objective of this research was to evaluate two perchlorate bioremediation strategies using indigenous soil bact...

  2. Perchlorate and nitrate in leafy vegetables of North America.

    Science.gov (United States)

    Sanchez, C A; Crump, K S; Krieger, R I; Khandaker, N R; Gibbs, J P

    2005-12-15

    In previous studies trace levels of perchlorate were found in lettuce (Lactuca sativa L.) irrigated with Colorado River water, which is contaminated with low levels of perchlorate from aerospace and defense related industries. In this paper, we report the results of a survey conducted across North America to evaluate the occurrence of perchlorate in leafy vegetables produced outside the lower Colorado River region, and evaluate the relative iodide uptake inhibition potential to perchlorate and nitrate in these leafy vegetables. Conventionally and organically produced lettuce and other leafy vegetable samples were collected from production fields and farmers' markets in the central and coastal valleys of California, New Mexico, Colorado, Michigan, Ohio, New York, Quebec, and New Jersey. Results show that 16% of the conventionally produced samples and 32% of the organically produced samples had quantifiable levels of perchlorate using ion chromatography. Estimated perchlorate exposure from organically produced leafy vegetables was approximately 2 times that of conventional produce, but generally less than 10% of the reference dose recommended by the National Academy of Sciences. Furthermore, the iodide uptake inhibition potential of perchlorate was less than 1% of that of the nitrate present. These data are consistent with those of other reported perchlorate survey work with lettuce, bottled water, breast milk, dairy milk, and human urine, and suggest a wide national presence of perchlorate. PMID:16475313

  3. Atmospheric Production of Perchlorate on Earth and Mars

    Science.gov (United States)

    Claire, M.; Catling, D. C.; Zahnle, K. J.

    2009-12-01

    Natural production and preservation of perchlorate on Earth occurs only in arid environments. Isotopic evidence suggests a strong role for atmospheric oxidation of chlorine species via pathways including ozone or its photochemical derivatives. As the Martian atmosphere is both oxidizing and drier than the driest places on Earth, we propose an atmospheric origin for the Martian perchlorates measured by NASA's Phoenix Lander. A variety of hypothetical formation pathways can be proposed including atmospheric photochemical reactions, electrostatic discharge, and gas-solid reactions. Here, we investigate gas phase formation pathways using a 1-D photochemical model (Catling et al. 2009, accepted by JGR). Because perchlorate-rich deposits in the Atacama desert are closest in abundance to perchlorate measured at NASA's Phoenix Lander site, we start with a study of the means to produce Atacama perchlorate. We found that perchlorate can be produced in sufficient quantities to explain the abundance of perchlorate in the Atacama from a proposed gas phase oxidation of chlorine volatiles to perchloric acid. These results are sensitive to estimated reaction rates for ClO3 species. The feasibility of gas phase production for the Atacama provides justification for further investigations of gas phase photochemistry as a possible source for Martian perchlorate. In addition to the Atacama results, we will present a preliminary study incorporating chlorine chemistry into an existing Martian photochemical model (Zahnle et al. JGR 2008).

  4. Interaction of perchlorate and trichloroethene bioreductions in mixed anaerobic culture.

    Science.gov (United States)

    Wen, Li-Lian; Yang, Qiang; Zhang, Zhao-Xin; Yi, Yang-Yi; Tang, Youneng; Zhao, He-Ping

    2016-11-15

    This work evaluated the interaction of perchlorate and trichloroethene (TCE), two common co-contaminants in groundwater, during bioreduction in serum bottles containing synthetic mineral salts media and microbial consortia. TCE at concentrations up to 0.3mM did not significantly affect perchlorate reduction; however, perchlorate concentrations higher than 0.1mM made the reduction of TCE significantly slower. Perchlorate primarily inhibited the reduction of vinyl chloride (VC, a daughter product of TCE) to ethene. Mechanistic analysis showed that the inhibition was mainly because perchlorate reduction is thermodynamically more favorable than reduction of TCE and its daughter products and not because of toxicity due to accumulation of dissolved oxygen produced during perchlorate reduction. As the initial perchlorate concentration increased from 0 to 600mg/L in a set of serum bottles, the relative abundance of Rhodocyclaceae (a putatively perchlorate-reducing genus) increased from 6.3 to 80.6%, while the relative abundance of Dehalococcoides, the only known genus that is able to reduce TCE all the way to ethene, significantly decreased. Similarly, the relative abundance of Proteobacteria (a phylum to which most known perchlorate-reducing bacteria belong) increased from 22% to almost 80%. PMID:27449607

  5. USE OF TWO DIGESTION METHODS IN THE EVALUATION OF CHROMIUM CONTENT IN CATTLE'S MEAT SUPPLEMENTED WITH CHROMIUM CHELATES

    Directory of Open Access Journals (Sweden)

    R. L. T. de Andrade

    2015-06-01

    Full Text Available The present study aimed to analyze the chromium content in beef using two digestion methods. There were used samples from 24 18-month-old male cattle, and twelve of them were supplemented and twelve were not supplemented with chromium chelate. These samples were evaluated by atomic absorption spectroscopy, previously submitted to digestion method using nitric acid (65% with hydrogen peroxide (35% and to digestion method, using solution of nitric perchloric acid in the proportion 3:1. Immediately after the slaughter, the carcasses were sent to sanitary maturation. After 24 hours, samples between 12th and 13th rib in the muscle Longissimus Thoracis were taken. For evaluation, it was used completely randomized design (Die and analysis of variance (ANOVA at 5% of significance level. The results didn't evidenced any significant difference (p>0,05 between the (cromo content, regardless the supplementation. The same happened with the digestion methods used.

  6. Perchlorate in the Great Lakes: isotopic composition and origin.

    Science.gov (United States)

    Poghosyan, Armen; Sturchio, Neil C; Morrison, Candice G; Beloso, Abelardo D; Guan, Yunbin; Eiler, John M; Jackson, W Andrew; Hatzinger, Paul B

    2014-10-01

    Perchlorate is a persistent and mobile contaminant in the environment with both natural and anthropogenic sources. Stable isotope ratios of oxygen (δ(18)O, Δ(17)O) and chlorine (δ(37)Cl) along with the abundance of the radioactive isotope (36)Cl were used to trace perchlorate sources and behavior in the Laurentian Great Lakes. These lakes were selected for study as a likely repository of recent atmospheric perchlorate deposition. Perchlorate concentrations in the Great Lakes range from 0.05 to 0.13 μg per liter. δ(37)Cl values of perchlorate from the Great Lakes range from +3.0‰ (Lake Ontario) to +4.0‰ (Lake Superior), whereas δ(18)O values range from -4.1‰ (Lake Superior) to +4.0‰ (Lake Erie). Great Lakes perchlorate has mass-independent oxygen isotopic variations with positive Δ(17)O values (+1.6‰ to +2.7‰) divided into two distinct groups: Lake Superior (+2.7‰) and the other four lakes (∼+1.7‰). The stable isotopic results indicate that perchlorate in the Great Lakes is dominantly of natural origin, having isotopic composition resembling that measured for indigenous perchlorate from preindustrial groundwaters of the western USA. The (36)Cl/Cl ratio of perchlorate varies widely from 7.4 × 10(-12) (Lake Ontario) to 6.7 × 10(-11) (Lake Superior). These (36)ClO4(-) abundances are consistent with an atmospheric origin of perchlorate in the Great Lakes. The relatively high (36)ClO4(-) abundances in the larger lakes (Lakes Superior and Michigan) could be explained by the presence of (36)Cl-enriched perchlorate deposited during the period of elevated atmospheric (36)Cl activity following thermonuclear bomb tests in the Pacific Ocean. PMID:25171443

  7. High ozone increases soil perchlorate but does not affect foliar perchlorate content

    Science.gov (United States)

    Ozone (O3) is implicated in the natural source inventory of perchlorate (ClO4-), a hydrophilic salt that migrates to ground water and interferes with uptake of iodide in mammals, including humans. Tropospheric O3 is elevated in many areas. We previously showed (Grantz et al., 2013; Environmental Pol...

  8. Oxidation of chromium telluride

    International Nuclear Information System (INIS)

    The authors study the interaction between chromium telluride and oxygen at elevated temperatures in view of its application in semiconductor technology. Thermodynamic analysis of the oxidation process and experimental data showed that the alloys of chromium telluride suffer oxidation in the presence of even traces of oxygen in a gaseous medium. Chromium telluride oxidation is a complex process that gives rise to various oxides and is accompanied by partial sublimation

  9. Oxidation of chromium telluride

    Energy Technology Data Exchange (ETDEWEB)

    Pakhomovskaya, N.S.; Iorga, E.V.; Sheveleva, T.F.; Solov' eva, A.E.

    1986-03-01

    The authors study the interaction between chromium telluride and oxygen at elevated temperatures in view of its application in semiconductor technology. Thermodynamic analysis of the oxidation process and experimental data showed that the alloys of chromium telluride suffer oxidation in the presence of even traces of oxygen in a gaseous medium. Chromium telluride oxidation is a complex process that gives rise to various oxides and is accompanied by partial sublimation.

  10. PERCHLORATE IDENTIFICATION IN FERTILIZERS AND ACCUMULATION IN LETTUCE SEEDLINGS

    Science.gov (United States)

    Perchlorate has contaminated groundwater, drinking water and soils at several locations in the U.S. The primary source of contamination at sites that have been investigated to date seems to be from industrial and military operations that use Perchlorate as an oxidizing agent. How...

  11. Thermal decomposition of ammonium perchlorate during gamma-ray irradiation

    International Nuclear Information System (INIS)

    To assess radiation damage effects in propellants, pyrotechnics, and similar materials, thermal decomposition measurements were made on ammonium perchlorate powders and crystals during gamma-ray irradiation. Gas evolution studies were made on single crystals and powders of ammonium perchlorate, both at room temperature and at 2270C. The results are discussed. (U.S.)

  12. Bioremediation Potential of Perchlorate Contaminated Deep Vadose Zone

    Science.gov (United States)

    Gal, H.; Ronen, Z.; Weisbrod, N.; Dahan, O.; Nativ, R.

    2007-12-01

    Widespread perchlorate contamination was found in the vadose zone near a plant that manufactures ammonium perchlorate above the coastal aquifer of Israel in Ramat Hasharon. As part of the plant's operations, untreated industrial wastewater was disposed of for over 30 years in unlined wastewater ponds and nearby washes, causing contamination of the unsaturated zone (up to 2200 mg kg-1 sediment at a depth of 20 m) and the groundwater below it (up to 300 mg L-1). In this study, we examined the potential for microbial metabolism of perchlorate reduction in the contaminated deep vadose zone profile by native microbial communities. Microbial reduction of perchlorate was found in three of the four sediment samples taken from different depths. The sediments taken from 1 m (shallowest) and 35 m (deepest- close to the water table) showed the fastest degradation rates, while the sediment taken from 15 m showed the slowest rate. No perchlorate reduction was observed in the sediment taken from 20 m, where perchlorate concentrations were highest. These results were correlated to the viable microorganism counts in the profile. In experiments in which the effect of nitrate was examined, the lag time for perchlorate degradation was found to be inversely correlated to the initial nitrate concentration, while the perchlorate-reduction rates were faster in treatments with higher initial nitrate concentrations. We found no perchlorate degradation as long as nitrate was present in the system: perchlorate reduction was initiated only after all of the nitrate had been reduced. Nitrate-reduction rates were correlated to the initial nitrate concentrations and no lag period was observed. Nitrite was temporarily accumulated during nitrate reduction and was totally reduced, like nitrate, after 4 days. Count of viable microbial communities as well as PCR analysis of the chlorite dismutase gene in the native microbial population exposed to high concentrations of perchlorate (10,000-20,000 mg L-1

  13. Experimental chlorine stable isotope fractionation of perchlorate respiring bacteria

    Science.gov (United States)

    Ader, M.; Coleman, M.; Coates, J.; Chaudhuri, S.

    2006-12-01

    Perchlorate natural occurrences on earth are very limited and seem restricted to extremely arid environments such as nitrate deposits of the Atacama Desert of northern Chile, where perchlorate contents can reach 0.1 to 1%. Anthropogenically sourced perchlorate however is extensively used as a major component of explosives and rocket fuels. Careless disposal of these highly soluble and very stable perchlorates locally led to the contamination of drinking water, now recognised as posing a significant health threat. Recent studies have demonstrated that some microorganisms are able to completely reduce perchlorate to innocuous chloride, and offer a great potential for the bioremediation of contaminated waters. Provided that the isotopic fractionation associated with this reduction is significant, the measurement of the chloride isotopic composition of contaminated water is a powerful tool for monitoring the progress of in-situ remediation. We report here, the characterisation of the isotopic fractionation associated with perchlorate reduction performed by Dechlorosoma suillum strain PS during 3 culture experiments performed in a batch fermentor (anoxic, 37°°C, pH =7). The basal medium contained acetate as the electron donor and perchlorate as the electron acceptor. When possible, chloride salts were replaced by sulphate salts so as to lower the initial chloride content. The paired chlorine isotopic compositions of chloride and perchlorate in solutions sampled throughout the experiment were measured using the method described in Ader et al. 2001. The fractionation between chloride and perchlorate was calculated independently for each sample, using on the one hand the chloride content and isotopic composition and on the other hand the perchlorate content and isotopic composition. The results show that the fractionation is constant within error throughout the experiment for the 3 experiments with a weighted mean of -14.94±0.14‰. This value is much lower than the

  14. Proteomic detection of proteins involved in perchlorate and chlorate metabolism.

    Science.gov (United States)

    Bansal, Reema; Deobald, Lee A; Crawford, Ronald L; Paszczynski, Andrzej J

    2009-09-01

    Mass spectrometry and a time-course cell lysis method were used to study proteins involved in perchlorate and chlorate metabolism in pure bacterial cultures and environmental samples. The bacterial cultures used included Dechlorosoma sp. KJ, Dechloromonas hortensis, Pseudomonas chloritidismutans ASK-1, and Pseudomonas stutzeri. The environmental samples included an anaerobic sludge enrichment culture from a sewage treatment plant, a sample of a biomass-covered activated carbon matrix from a bioreactor used for treating perchlorate-contaminated drinking water, and a waste water effluent sample from a paper mill. The approach focused on detection of perchlorate (and chlorate) reductase and chlorite dismutase proteins, which are the two central enzymes in the perchlorate (or chlorate) reduction pathways. In addition, acetate-metabolizing enzymes in pure bacterial samples and housekeeping proteins from perchlorate (or chlorate)-reducing microorganisms in environmental samples were also identified. PMID:19199051

  15. Thermal decomposition of beryllium perchlorate tetrahydrate

    International Nuclear Information System (INIS)

    Thermal decomposition of Be(ClO4)2x4H2O was studied by the differential flow technique in the helium stream. The kinetics was followed by an exchange reaction of the perchloric acid appearing by the decomposition with potassium carbonate. The rate of CO2 liberation in this process was recorded by a heat conductivity detector. The exchange reaction yielding CO2 is quantitative, it is not the limiting one and it does not distort the kinetics of the process of perchlorate decomposition. The solid products of decomposition were studied by infrared and NMR spectroscopy, roentgenography, thermography and chemical analysis. A mechanism suggested for the decomposition involves intermediate formation of hydroxyperchlorate: Be(ClO4)2x4H2O → Be(OH)ClO4+HClO4+3H2O; Be(OH)ClO4 → BeO+HClO4. Decomposition is accompained by melting of the sample. The mechanism of decomposition is hydrolytic. At room temperature the hydroxyperchlorate is a thick syrup-like compound crystallizing after long storing

  16. Hair chromium concentration and chromium excretion in tannery workers.

    OpenAIRE

    Saner, G; Yüzbasiyan, V; Cigdem, S

    1984-01-01

    Hair and urine samples were collected from 34 male tannery workers and from 12 normal adults. Eighteen of the workers dealt directly with chromium and the remaining 16 (controls) worked in the offices and kitchen of the same factory. All were found to be clinically healthy. Chromium was determined by flameless atomic absorption spectroscopy. When compared with normal adult values, urinary chromium concentration, Cr/Creatinine ratio, daily chromium excretion, and hair chromium, concentrations ...

  17. Perchlorates as Powerful Catalysts in Many Important Organic Transformations

    Institute of Scientific and Technical Information of China (English)

    G. Bartoli; L. Sambri; M. Locatelli

    2005-01-01

    @@ 1Introduction For long times, metallic perchlorates have been considered dangerous compounds[1] in that they function as explosives and as incontrollable oxidizers. Therefore, the fear of the great hazard connected with their manufacture and uses had prevented an extensive use both in research laboratories and in industrial processes[2].However, recently it has been cleared that this bad reputation is due to the mistaken association of metallic perchlorates with the oxidizing potential of perchloric acid and the pyrotechnic performances of NH4ClO4.

  18. Effects of Perchlorate on Organic Molecules under Simulated Mars Conditions

    Science.gov (United States)

    Carrier, B. L.; Kounaves, S. P.

    2014-12-01

    Perchlorate (ClO4-) was discovered in the northern polar region of Mars by the Mars Phoenix Lander in 2008 and has also been recently detected by the Curiosity Rover in Gale Crater [1,2]. Perchlorate has also been shown to be formed under current Mars conditions via the oxidation of mineral chlorides, further supporting the theory that perchlorate is present globally on Mars [3]. The discovery of perchlorate on Mars has raised important questions about the effects of perchlorate on the survival and detection of organic molecules. Although it has been shown that pyrolysis in the presence of perchlorate results in the alteration or destruction of organic molecules [4], few studies have been conducted on the potential effects of perchlorate on organic molecules under martian surface conditions. Although perchlorate is typically inert under Mars-typical temperatures [5], perchlorate does absorb high energy UV radiation, and has been shown to decompose to form reactive oxychlorine species such as chlorite (ClO2-) when exposed to martian conditions including UV or ionizing radiation [6,7]. Here we investigate the effects of perchlorate on the organic molecules tryptophan, benzoic acid and mellitic acid in order to determine how perchlorate may alter these compounds under Mars conditions. Experiments are performed in a Mars Simulation Chamber (MSC) capable of reproducing the temperature, pressure, atmospheric composition and UV flux found on Mars. Soil simulants are prepared consisting of SiO2 and each organic, as well as varying concentrations of perchlorate salts, and exposed in the MSC. Subsequent to exposure in the MSC samples are leached and the leachate analyzed by HPLC and LC-MS to determine the degree of degradation of the original organic and the identity of any potential decomposition products formed by oxidation or chlorination. References: [1] Kounaves et al., J. Geophys. Res. Planets, Vol. 115, p. E00E10, 2010 [2] Glavin et al., J. Geophys. Res. Planets, Vol

  19. High-Purity Chromium Targets

    OpenAIRE

    Rudoy, A.; Milman, Yu.; Korzhova, N.

    1995-01-01

    A procedure for producing large-scale chromium ingots by means of induction-arc melting was developed. From the high-purity, low-alloyed chromium ingots obtained, chromium targets were produced by of thermoplastic treatment techniques. The method of electron-beam evaporation of high-purity chromium was also used for production of targets.

  20. Simultaneous removal of perchlorate and energetic compounds in munitions wastewater by zero-valent iron and perchlorate-respiring bacteria.

    Science.gov (United States)

    Ahn, Se Chang; Hubbard, Brian; Cha, Daniel K; Kim, Byung J

    2014-01-01

    Ammonium perchlorate is one of the main constituents in Army's insensitive melt-pour explosive, PAX-21 in addition to RDX and 2,4-dinitroanisole (DNAN). The objective of this study is to develop an innovative treatment process to remove both perchlorate and energetic compounds simultaneously from PAX-21 production wastewater. It was hypothesized that the pretreatment of PAX-21 wastewater with zero-valent iron (ZVI) would convert energetic compounds to products that are more amenable for biological oxidation and that these products serve as electron donors for perchlorate-reducing bacteria. Results of batch ZVI reduction experiments showed that DNAN was completely reduced to 2,4-diaminoanisole and RDX was completely reduced to formaldehyde. Anaerobic batch biodegradation experiments showed that perchlorate (30 mg L(-1)) in ZVI-treated PAX-21 wastewater was decreased to an undetectable level after 5 days. Batch biodegradation experiments also confirmed that formaldehyde in ZVI-treated wastewater was the primary electron donor for perchlorate-respiring bacteria. The integrated iron-anaerobic bioreactor system was effective in completely removing energetic compounds and perchlorate from the PAX-21 wastewater without adding an exogenous electron donor. This study demonstrated that ZVI pretreatment not only removed energetic compounds, but also transformed energetic compounds to products that can serve as the source of electrons for perchlorate-respiring bacteria. PMID:24410688

  1. Microstructural characterisation of chromium slags

    OpenAIRE

    Burja, J.; F. Tehovnik; Vode, F.; Arh, B.

    2015-01-01

    In this chromium slags that form during melting of chromium alloyed steels are examined. During melting and oxidation of these steel grades a considerable amount of chromium is lost, and gained back with slag reduction. Laboratory experiments were performed to study the mechanism of chromium oxide reduction by silicon. Slags chemistry and phase composition have a strong effect on the steelmaking process. Phase analysis revealed two types of chromium oxides, calcium chromites and chromite spin...

  2. The NAS Perchlorate Review: Adverse Effects?

    Energy Technology Data Exchange (ETDEWEB)

    Johnston, Richard B.; Corley, Richard; Cowan, Linda; Utiger, Robert D.

    2005-11-01

    To the editor: Drs. Ginsberg and Rice argue that the reference dose for perchlorate of 0.0007 mg/kg per day recommended by the National Academies’ Committee to Assess the Health Implications of Perchlorate Ingestion is not adequately protective. As members of the committee, we disagree. Ginsberg and Rice base their conclusion on three points. The first involves the designation of the point of departure as a NOEL (no-observed-effect level) versus a LOAEL (lowest-observed-adverse- effect level). The committee chose as its point of departure a dose of perchlorate (0.007 mg/kg per day) that when given for 14 days to 7 normal subjects did not cause a significant decrease in the group mean thyroid iodide uptake (Greer et al. 2002). Accordingly, the committee considered it a NOEL. Ginsberg and Rice focus on the fact that only 7 subjects were given that dose, and they 1seem to say that attention should be paid only to the results in those subjects in whom there was a 1fall in thyroid iodide uptake, and that the results in those in whom there was no fall or an increase should be ignored. They consider the dose to be a LOAEL because of the fall in uptake in those few subjects. It is important to note that a statistically significant decrease of, for example, 5% or even 10%, would not be biologically important and, more important, would not be sustained. For example, in another study (Braverman et al. 2004), administration of 0.04 mg/kg per day to normal subjects for 6 months had no effect on thyroid iodide uptake when measured at 3 and 6 months, and no effect on serum thyroid hormone or thyrotropin concentrations measured monthly (inspection of Figure 5A in the paper by Greer et al. suggests that this dose would inhibit thyroid iodide uptake by about 25% if measured at 2 weeks). The second issue involves database uncertainty. In clinical studies, perchlorate has been administered prospectively to 68 normal subjects for 2 weeks to 6 months. In one study (Brabant et al. 1992

  3. Substoichiometric extraction of chromium

    International Nuclear Information System (INIS)

    Substoichiometric extraction of chromium with tetraphenylarsonium chloride (TPACl), tri-n-octylamine (TNOA), diethylammonium diethyldithiocarbamate (DDDC) and ammonium pyrrolidinedithiocarbamate (APDC) was examined in detail. Chromium can be extracted substoichiometrically in a pH range, which is 1.1-2.6 for the TPACl compound, 0.6-2.3 for the TNOA compound, 5.1-6.4 for the DDDC chelate and 3.9-4.9 for the APDC chelate. Chromium in high-purity calcium carbonate, Orchard Leaves (NBS SRM-1571) and Brewers Yeast (NBS SRM-1569) was determined by neutron activation analysis combined with substoichiometric extraction by DDDC and APDC. The values of 2.0+-0.02 ppm and 2.6+-0.2 ppm were obtained for Brewers Yeast and Orchard Leaves, respectively. These values were in good agreement with those reported by NBS. The reaction mechanism and the reaction ratio between hexavalent chromium and dithiocarbamate are also discussed. (author)

  4. Chromium in diet

    Science.gov (United States)

    ... Chromium deficiency may be seen as impaired glucose tolerance. It occurs in older people with type 2 ... PhD, and the A.D.A.M. Editorial team. Related MedlinePlus Health Topics Minerals Browse the Encyclopedia ...

  5. Behavioral response of dissimilatory perchlorate-reducing bacteria to different electron acceptors.

    Science.gov (United States)

    Sun, Yvonne; Gustavson, Ruth L; Ali, Nadia; Weber, Karrie A; Westphal, Lacey L; Coates, John D

    2009-10-01

    The response behavior of three dissimilatory perchlorate-reducing bacteria to different electron acceptors (nitrate, chlorate, and perchlorate) was investigated with two different assays. The observed response was species-specific, dependent on the prior growth conditions, and was inhibited by oxygen. We observed attraction toward nitrate when Dechloromonas aromatica strain RCB and Azospira suillum strain PS were grown with nitrate. When D. aromatica and Dechloromonas agitata strain CKB were grown with perchlorate, both responded to nitrate, chlorate, and perchlorate. When A. suillum was grown with perchlorate, the organism responded to chlorate and perchlorate but not nitrate. A gene replacement mutant in the perchlorate reductase subunit (pcrA) of D. aromatica resulted in a loss of the attraction response toward perchlorate but had no impact on the nitrate response. Washed-cell suspension studies revealed that the perchlorate grown cells of D. aromatica reduced both perchlorate and nitrate, while A. suillum cells reduced perchlorate only. Based on these observations, energy taxis was proposed as the underlying mechanism for the responses to (per)chlorate by D. aromatica. To the best of our knowledge, this study represents the first investigation of the response behavior of perchlorate-reducing bacteria to environmental stimuli. It clearly demonstrates attraction toward chlorine oxyanions and the unique ability of these organisms to distinguish structurally analogous compounds, nitrate, chlorate, and perchlorate and respond accordingly. PMID:19533120

  6. The carcinogenicity of chromium

    OpenAIRE

    Norseth, Tor

    1981-01-01

    The carcinogenicity of chromium compounds is reviewed with specific attention to the gaps in knowledge for risk estimation and research needs. The most important problems at present are whether trivalent chromium compounds cause cancer, and whether there is a difference in cancer causing effects between the soluble and the slightly soluble hexavalent compounds in the practical exposure situation. Dose estimates for risk estimation based on epidemiological investigations are also lacking. Pres...

  7. Perchlorate Reductase Is Distinguished by Active Site Aromatic Gate Residues.

    Science.gov (United States)

    Youngblut, Matthew D; Tsai, Chi-Lin; Clark, Iain C; Carlson, Hans K; Maglaqui, Adrian P; Gau-Pan, Phonchien S; Redford, Steven A; Wong, Alan; Tainer, John A; Coates, John D

    2016-04-22

    Perchlorate is an important ion on both Earth and Mars. Perchlorate reductase (PcrAB), a specialized member of the dimethylsulfoxide reductase superfamily, catalyzes the first step of microbial perchlorate respiration, but little is known about the biochemistry, specificity, structure, and mechanism of PcrAB. Here we characterize the biophysics and phylogeny of this enzyme and report the 1.86-Å resolution PcrAB complex crystal structure. Biochemical analysis revealed a relatively high perchlorate affinity (Km = 6 μm) and a characteristic substrate inhibition compared with the highly similar respiratory nitrate reductase NarGHI, which has a relatively much lower affinity for perchlorate (Km = 1.1 mm) and no substrate inhibition. Structural analysis of oxidized and reduced PcrAB with and without the substrate analog SeO3 (2-) bound to the active site identified key residues in the positively charged and funnel-shaped substrate access tunnel that gated substrate entrance and product release while trapping transiently produced chlorate. The structures suggest gating was associated with shifts of a Phe residue between open and closed conformations plus an Asp residue carboxylate shift between monodentate and bidentate coordination to the active site molybdenum atom. Taken together, structural and mutational analyses of gate residues suggest key roles of these gate residues for substrate entrance and product release. Our combined results provide the first detailed structural insight into the mechanism of biological perchlorate reduction, a critical component of the chlorine redox cycle on Earth. PMID:26940877

  8. Determination of Perchlorate in Bottled Water from Italy

    Directory of Open Access Journals (Sweden)

    Patrizia Iannece

    2013-06-01

    Full Text Available Perchlorate is regarded as an emerging persistent inorganic contaminant. It is widely known that perchlorate is an endocrine disruptor as it competitively inhibits iodide transport in the thyroid gland. As drinking water is the major source of human exposure to perchlorate, its occurrence in commercially available bottled waters purchased in different regions of Italy was investigated. Perchlorate was measured using the rapid, sensitive, and selective LC-ESI-MS/MS (liquid chromatography-electrospray tandem mass spectrometry method by multiple reaction monitoring (MRM of the transition 98.8→82.8, which corresponds to the loss of one oxygen atom in the perchlorate ion (ClO4−→ClO3−. The chlorine isotope ratio (35Cl/37Cl was used as a confirmation tool. The limit of quantification (LOQ for this method was 5 ng/L, and the recovery ranged from 94% to 108%. Perchlorate was detected in 44 of the 62 drinking waters tested, with concentrations ranging from <5 to 75 ng/L. These values are similar in magnitude to those reported in drinking water from the USA and do not pose an immediate health concern.

  9. Chemolithotrophic perchlorate reduction linked to the oxidation of elemental sulfur.

    Science.gov (United States)

    Ju, Xiumin; Field, Jim A; Sierra-Alvarez, Reyes; Salazar, Margarita; Bentley, Harold; Bentley, Richard

    2007-04-15

    Perchlorate (ClO(4)(-)) contamination of ground and surface water has been recently recognized as a widespread environmental problem. Biological methods offer promising perspectives of perchlorate remediation. Facultative anaerobic bacteria couple the oxidation of organic and inorganic electron-donating substrates to the reduction of perchlorate as a terminal electron acceptor, converting it completely to the benign end-product, chloride. Insoluble inorganic substrates are of interest for low maintenance bioreactor or permeable reactive barrier systems because they can provide a long-term supply of electron donor without generating organic residuals. The main objective of this research was to investigate the feasibility of utilizing elemental sulfur (S(0)) as an insoluble electron donor for the biological reduction of perchlorate. A chemolithotrophic enrichment culture derived from aerobic activated sludge was obtained which effectively coupled the oxidation of elemental sulfur to sulfate with the reduction of perchlorate to chloride and gained energy from the process for cell growth. The enrichment culture grew at a rate of 0.41 or 0.81 1/d in the absence and presence of added organic carbon for cell growth, respectively. The enrichment culture was also shown to carry out sulfur disproportionation to a limited extent as evidenced by the formation of sulfide and sulfate in the absence of added electron acceptor. When nitrate and perchlorate were added together, the two electron acceptors were removed simultaneously after an initial partial decrease in the nitrate concentration. PMID:17009322

  10. Oxidation of some disubstituted anisole derivatives with ceric perchlorate in perchloric acid solution

    International Nuclear Information System (INIS)

    The influence of concentration of particular reagents on the kinetics of Ce(IV) reduction by 2,6-dimethyl and 3,5-dimethyl-anisole as well as 2-methoxy-5-methyl- and 4-methoxy-2-methyl-aniline in perchloric acid solution was investigated, establishing the stoichiometry of these processes. Some intermediate products - macromolecular, derivatives of p-benzoquinone and 4,4'-diphenoquinone - were separated and identified. The effects of substituents and the conditions of performed oxidation processes on the kind and yields of the resultant products were considered. (author). 22 refs, 1 fig., 1 tab

  11. Perchlorate in The Great Lakes: Distribution, Isotopic Composition and Origin

    Science.gov (United States)

    Poghosyan, A.; Sturchio, N. C.; Jackson, W. A.; Guan, Y.; Eiler, J. M.; Hatzinger, P. B.

    2013-12-01

    Concentrations, stable chlorine and oxygen isotopic compositions, and 36Cl abundances of perchlorate were investigated in the five Laurentian Great Lakes. Samples were collected during monitoring cruises in 2007 and 2008 of the U.S. EPA's RV Lake Guardian and in 2010 at the water supply intake of Marquette, MI on the southern shore of Lake Superior. Concentrations of perchlorate were measured by IC/MS/MS at 24 locations, including one or two depth profiles in each lake. Mean concentrations (μg/L) are: Superior, 0.06 × 0.01; Michigan, 0.10 × 0.01; Huron, 0.11 × 0.01; Erie, 0.08 × 0.01, and Ontario, 0.09 × 0.01. Concentration vs. depth is nearly constant in each lake, indicating well-mixed conditions. Perchlorate was extracted from near-surface water by passing 15,000 to 80,000 L of water through 1-L cartridges containing Purolite A530E bifunctional anion-exchange resin. In the laboratory, perchlorate was eluted from the resin, purified, and precipitated as a >99% pure crystalline phase. Milligram amounts were recovered from each lake. Chlorine and oxygen isotopic analyses were performed at Caltech using the Cameca 7f-GEO SIMS instrument, following validation of the SIMS method with analyses of USGS-37 and USGS-38 isotopic reference materials. Results indicate a relatively narrow range in δ37Cl values (+2.9 to +3.9 ‰) and a wider range in δ18O values (-4.0 to +4.1 ‰), with a general geographic trend of increasing δ18O from west to east. Oxygen-17 was measured at UIC using dual-inlet IRMS of O2 produced by decomposition of KClO4. Great Lakes perchlorate has mass-independent oxygen isotopic variations with positive Δ17O values (+1.6 ‰ to +2.7 ‰) divided into two distinct groups: Lake Superior (+2.7 ‰) and the other four lakes (~ +1.7 ‰). The isotopic data indicate that perchlorate is dominantly of natural origin, having stable isotopic compositions resembling those of perchlorate from pre-industrial groundwaters in the western USA. The 36Cl

  12. Obtaining decorative chromium plating from trivalent chromium solutions

    OpenAIRE

    Óscar Javier Suárez García

    2010-01-01

    The present work was aimed at a qualitative evaluation, in the laboratory, of different alternatives for assembling and operating a trivalent chromium bath for decorative chromium plating. Different chromium concentration solutions and different complexing agents were used. The initial result of this analysis was that chloride, formate and acetate solutions produced the best results. Solution preparation conditions were evaluated: temperature, chromium III complex formation time and also ...

  13. Perchlorate, iodine supplements, iodized salt and breast milk iodine content

    International Nuclear Information System (INIS)

    This study was undertaken to determine if increasing maternal iodine intake through single dose tablets will decrease breast milk concentrations of the iodine-uptake inhibitor, perchlorate, through competitive inhibition. We also sought to determine if the timing of supplementation influences the fraction of iodine excreted in milk versus urine and to compare the effectiveness of iodized salt as a means of providing iodine to breastfed infants. Thirteen women who did not use supplements, seven of whom used iodized salt and six of whom used non-iodized salt, submitted four milk samples and a 24-h urine collection daily for three days. Women repeated the sampling protocol for three more days during which ∼ 150 μg of iodine were taken in the evening and again for three days with morning supplementation. Samples were analyzed using isotope-dilution inductively-coupled plasma-mass spectrometry for iodine and isotope-dilution ion chromatography-tandem mass spectrometry for perchlorate. No statistically significant differences were observed in milk iodine or perchlorate concentrations during the two treatment periods. Estimated perchlorate intake was above the U.S. National Academy of Sciences suggested reference dose for most infants. Single daily dose iodine supplementation was not effective in decreasing milk perchlorate concentrations. Users of iodized salt had significantly higher iodine levels in milk than non-users. Iodized salt may be a more effective means of iodine supplementation than tablets. - Highlights: ► Estimated infant exposures to perchlorate were, on a μg/kg basis, ∼ 5 × higher than those of mothers. ► Daily supplements are less effective than iodized salt in providing iodine to lactating women. ► Low iodine and high perchlorate in milk may place infants at risk of iodine deficiency.

  14. Perchlorate, iodine supplements, iodized salt and breast milk iodine content

    Energy Technology Data Exchange (ETDEWEB)

    Kirk, Andrea B. [Department of Epidemiology, School of Public Health, University of North Texas Health Sciences Center, 3500 Camp Bowie Blvd., Fort Worth, TX 76107 (United States); Kroll, Martina; Dyke, Jason V.; Ohira, Shin-Ichi; Dias, Rukshan A.; Dasgupta, Purnendu K. [Department of Chemistry and Biochemistry, 700 Planetarium Place, University of Texas at Arlington, Arlington, TX 76019 (United States)

    2012-03-15

    This study was undertaken to determine if increasing maternal iodine intake through single dose tablets will decrease breast milk concentrations of the iodine-uptake inhibitor, perchlorate, through competitive inhibition. We also sought to determine if the timing of supplementation influences the fraction of iodine excreted in milk versus urine and to compare the effectiveness of iodized salt as a means of providing iodine to breastfed infants. Thirteen women who did not use supplements, seven of whom used iodized salt and six of whom used non-iodized salt, submitted four milk samples and a 24-h urine collection daily for three days. Women repeated the sampling protocol for three more days during which {approx} 150 {mu}g of iodine were taken in the evening and again for three days with morning supplementation. Samples were analyzed using isotope-dilution inductively-coupled plasma-mass spectrometry for iodine and isotope-dilution ion chromatography-tandem mass spectrometry for perchlorate. No statistically significant differences were observed in milk iodine or perchlorate concentrations during the two treatment periods. Estimated perchlorate intake was above the U.S. National Academy of Sciences suggested reference dose for most infants. Single daily dose iodine supplementation was not effective in decreasing milk perchlorate concentrations. Users of iodized salt had significantly higher iodine levels in milk than non-users. Iodized salt may be a more effective means of iodine supplementation than tablets. - Highlights: Black-Right-Pointing-Pointer Estimated infant exposures to perchlorate were, on a {mu}g/kg basis, {approx} 5 Multiplication-Sign higher than those of mothers. Black-Right-Pointing-Pointer Daily supplements are less effective than iodized salt in providing iodine to lactating women. Black-Right-Pointing-Pointer Low iodine and high perchlorate in milk may place infants at risk of iodine deficiency.

  15. The analytical biochemistry of chromium.

    OpenAIRE

    Katz, S A

    1991-01-01

    The essentiality and carcinogenicity of chromium depend on its chemical form. Oxidation state and solubility are particularly important in determining the biological effects of chromium compounds. For this reason, total chromium measurements are of little value in assessing its nutritional benefits or its toxicological hazards. Aqueous sodium carbonate-sodium hydroxide solutions have been successfully used for extracting hexavalent chromium from a variety of environmental and biological matri...

  16. Developmental exposure to perchlorate alters synaptic transmission in hippocampus of the adult rat: in vivo studies.

    Science.gov (United States)

    Perchlorate, a contaminant found in food and water supplies throughout the USA, blocks iodine uptake into the thyroid gland to reduce circulating levels of thyroid hormone. Neurological function accompanying developmental exposure to perchlorate was evaluated in the present study...

  17. Chlorine isotopic composition of perchlorate in human urine as a means of distinguishing among exposure sources.

    Science.gov (United States)

    Poghosyan, Armen; Morel-Espinosa, Maria; Valentin-Blasini, Liza; Blount, Benjamin C; Ferreccio, Catterina; Steinmaus, Craig M; Sturchio, Neil C

    2016-05-01

    Perchlorate (ClO4(-)) is a ubiquitous environmental contaminant with high human exposure potential. Natural perchlorate forms in the atmosphere from where it deposits onto the surface of Earth, whereas synthetic perchlorate is manufactured as an oxidant for industrial, aerospace, and military applications. Perchlorate exposure can potentially cause adverse health effects in humans by interfering with the production of thyroid hormones through competitively blocking iodide uptake. To control and reduce perchlorate exposure, the contributions of different sources of perchlorate exposure need to be quantified. Thus, we demonstrate a novel approach for determining the contribution of different perchlorate exposure sources by quantifying stable and radioactive chlorine isotopes of perchlorate extracted from composite urine samples from two distinct populations: one in Atlanta, USA and one in Taltal, Chile (Atacama region). Urinary perchlorate from the Atlanta region resembles indigenous natural perchlorate from the western USA (δ(37)Cl=+4.1±1.0‰; (36)Cl/Cl=1 811 (±136) × 10(-15)), and urinary perchlorate from the Taltal, Chile region is similar to natural perchlorate in nitrate salt deposits from the Atacama Desert of northern Chile (δ(37)Cl=-11.0±1.0‰; (36)Cl/Cl=254 (±40) × 10(-15)). Neither urinary perchlorate resembled the isotopic pattern found in synthetic perchlorate. These results indicate that natural perchlorate of regional provenance is the dominant exposure source for the two sample populations, and that chlorine isotope ratios provide a robust tool for elucidating perchlorate exposure pathways. PMID:25805252

  18. Chromium in potatoes

    International Nuclear Information System (INIS)

    Chromium concentration in potatoes was determined, and tubes were labeled either intrinsically or extrinsically with radioactive chromate (51Cr). A labeled chromium complex was isolated from preparations of raw, baked, or fried potatoes and chromatographed on gel permeation media. Potato pulp and peel contained 1.63 and 2.70 μg of Cr/g tissue, respectively. There was no correlation between the two, nor did they respond similarly to changes of variety or locations. No significant differences were apparent in relative migration of the isolated complexes except between raw and cooked extrinsically labeled preparations

  19. Aluminum-based drinking-water treatment residuals: A novel sorbent for perchlorate removal

    International Nuclear Information System (INIS)

    Perchlorate contamination of aquifers and drinking-water supplies has led to stringent regulations in several states to reduce perchlorate concentrations in water at acceptable levels for human consumption. Several perchlorate treatment technologies exist, but there is significant cost associated with their use, and the majority of them are unable to degrade perchlorate to innocuous chloride. We propose the use of a novel sorbent for perchlorate, i.e. an aluminum-based drinking-water treatment residual (Al-WTR), which is a by-product of the drinking-water treatment process. Perchlorate sorption isotherms (23 ± 1 oC) showed that the greatest amount (65%) of perchlorate removed by the Al-WTR was observed with the lowest initial perchlorate load (10 mg L-1) after only 2 h of contact time. Increasing the contact time to 24 h, perchlorate removal increased from 65 to 76%. A significant correlation was observed between the amounts of perchlorate removed with evolved chloride in solution, suggesting degradation of perchlorate to chloride. - Drinking-water treatment residuals are a low-cost sorbent for perchlorate

  20. Chromium and aging

    Science.gov (United States)

    Aging is associated with increased blood glucose, insulin, blood lipids, and fat mass, and decreased lean body mass leading to increased incidences of diabetes and cardiovascular diseases. Improved chromium nutrition is associated with improvements in all of these variables. Insulin sensitivity de...

  1. Interaction between perchlorate and iodine in the metamorphosis of Hyla versicolor

    Science.gov (United States)

    Sparling, D.W.; Harvey, G.; Nzengung, V.

    2003-01-01

    Perchlorate (ClO4-) is a water-soluble, inorganic anion that is often combined with ammonium, potassium or other cations for use in industry and agriculture. Ammonium perchlorate, for example, is a potent oxidizer and is used in various military applications including rocket fuel. It has also been found in an historically widely used fertilizer, Chilean nitrate and in other fertilizers. It has been found in ground and surface waters of over 30 states and is considered a human health risk. Because of its similar atomic radius and volume, perchlorate competes with iodide for thyroid uptake and storage and thereby inhibits production of thyroid hormones. Amphibians may be particularly affected by perchlorate because they rely on the thyroid for metamorphosis. This study exposed early larval Hyla versicolor to concentrations of perchlorate ranging from 2.2 to 50 ppm to determine the effects of perchlorate on a native amphibian. In addition, three controls, 0 perchlorate, 0 perchlorate with 0.10 ppm iodide (C + I) and 50 ppm perchlorate + 0.10 ppm iodide (50 + I) were tested. Mortality (metamorphosis. The estimated EC50 for total inhibition of metamorphosis at 70 days of treatment was 3.63 ppm. There was no evidence of inhibition of development with the 50 + I, C + I, or controls, indicating that the presence of small concentrations of iodide could counter the effects of perchlorate. When tadpoles that had been inhibited by perchlorate were subsequently treated with iodide, development through prometamorphosis progressed but mortality was very high.

  2. Competitive microbial reduction of perchlorate and nitrate with a cathode directly serving as the electron donor

    International Nuclear Information System (INIS)

    Microbial reduction of perchlorate with an electrode as the electron donor represents an emerging technology for remediation of perchlorate contamination; it is important to know how perchlorate reduction behaves when nitrate, a co-contaminant of perchlorate is present. We reported that electrons derived from the electrode can be directly transferred to the bacteria with perchlorate or nitrate as the sole electron acceptor. The presence of nitrate, even at the 0.07 mM level, can slow reduction of perchlorate (0.70 mM) as a poised potential of -0.50 V (vs. SCE) was applied to the inoculated cathode. Increasing the concentration of nitrate resulted in a noticeable inhibitory effect on perchlorate reduction. When the nitrate concentration was 2.10 mM, reduction of 0.70 mM perchlorate was totally inhibited. Bacterial community analyses based on 16S rDNA gene analysis with denaturing gradient gel electrophoresis (DGGE) revealed that most of the bacteria newly enriched on the nitrate and/or perchlorate biocathodes were the known electrochemically active denitrifiers, which possibly prefer to reduce nitrate over perchlorate. These results show that nitrate is a more favorable electron acceptor than perchlorate in the bioelectrochemical system where the cathode directly serves as the electron donor

  3. Effect of nitrate, acetate and hydrogen on native perchlorate-reducing microbial communities and their activity in vadose soil

    OpenAIRE

    Nozawa-Inoue, Mamie; Jien, Mercy; Yang, Kun; Dennis E. Rolston; Hristova, Krassimira R.; Scow, Kate M.

    2011-01-01

    Effect of nitrate, acetate and hydrogen on native perchlorate-reducing bacteria (PRB) was examined by conducting microcosm tests using vadose soil collected from a perchlorate-contaminated site. The rate of perchlorate reduction was enhanced by hydrogen amendment and inhibited by acetate amendment, compared to unamendment. Nitrate was reduced before perchlorate in all amendments. In hydrogen-amended and unamended soils, nitrate delayed perchlorate reduction, suggesting the PRB preferentially ...

  4. Studies of chromium gettering

    International Nuclear Information System (INIS)

    Preliminary results have shown that hydrogen pumping by chromium is a surface effect. Unlike with titanium, the getter material used in many present day tokamaks, there is no significant diffusion into the bulk. Additional experiments have been carried out to measure the basic characteristics of chromium films for gases of interest in tokamak research. These gases include deuterium, oxygen and nitrogen. A vacuum system is described which allowed precise control of the test gas, a constant wall temperature and determination of the projected getter surface area. A quadrupole mass spectrometer, rather than simply a total pressure gauge, was utilized to measure the partial pressure of the test gas as well as the residual gas composition in the system. A quartz crystal monitor was used to measure film thickness. Pumping speeds and sticking coefficients are given as a function of surface coverage for each test gas. A comparison will be made with titanium films deposited in the same vacuum system and under similar conditions

  5. Branched polymeric media: Perchlorate-selective resins from hyperbranched polyethyleneimine

    KAUST Repository

    Chen, Dennis P.

    2012-10-02

    Perchlorate (ClO4 -) is a persistent contaminant found in drinking groundwater sources in the United States. Ion exchange (IX) with selective and disposable resins based on cross-linked styrene divinylbenzene (STY-DVB) beads is currently the most commonly utilized process for removing low concentrations of ClO4 - (10-100 ppb) from contaminated drinking water sources. However, due to the low exchange capacity of perchlorate-selective STY-DVB resins (∼0.5-0.8 eq/L), the overall cost becomes prohibitive when treating groundwater with higher concentration of ClO4 - (e.g., 100-1000 ppb). In this article, we describe a new perchlorate-selective resin with high exchange capacity. This new resin was prepared by alkylation of branched polyethyleneimine (PEI) beads obtained from an inverse suspension polymerization process. Batch and column studies show that our new PEI resin with mixed hexyl/ethyl quaternary ammonium chloride exchange sites can selectively extract trace amounts of ClO4 - from a makeup groundwater (to below detection limit) in the presence of competing ions. In addition, this resin has a strong-base exchange capacity of 1.4 eq/L, which is 1.75-2.33 times larger than those of commercial perchlorate-selective STY-DVB resins. The overall results of our studies suggest that branched PEI beads provide versatile and promising building blocks for the preparation of perchlorate-selective resins with high exchange capacity. © 2012 American Chemical Society.

  6. Sample processing method for the determination of perchlorate in milk

    International Nuclear Information System (INIS)

    In recent years, many different water sources and foods have been reported to contain perchlorate. Studies indicate that significant levels of perchlorate are present in both human and dairy milk. The determination of perchlorate in milk is particularly important due to its potential health impact on infants and children. As for many other biological samples, sample preparation is more time consuming than the analysis itself. The concurrent presence of large amounts of fats, proteins, carbohydrates, etc., demands some initial cleanup; otherwise the separation column lifetime and the limit of detection are both greatly compromised. Reported milk processing methods require the addition of chemicals such as ethanol, acetic acid or acetonitrile. Reagent addition is undesirable in trace analysis. We report here an essentially reagent-free sample preparation method for the determination of perchlorate in milk. Milk samples are spiked with isotopically labeled perchlorate and centrifuged to remove lipids. The resulting liquid is placed in a disposable centrifugal ultrafilter device with a molecular weight cutoff of 10 kDa, and centrifuged. Approximately 5-10 ml of clear liquid, ready for analysis, is obtained from a 20 ml milk sample. Both bovine and human milk samples have been successfully processed and analyzed by ion chromatography-mass spectrometry (IC-MS). Standard addition experiments show good recoveries. The repeatability of the analytical result for the same sample in multiple sample cleanup runs ranged from 3 to 6% R.S.D. This processing technique has also been successfully applied for the determination of iodide and thiocyanate in milk

  7. Catalytic Spectrophotometric Determination of Chromium

    OpenAIRE

    STOYANOVA, Angelina Miltcheva

    2005-01-01

    The catalytic effect of chromium(III) and chromium(VI) on the oxidation of sulfanilic acid by hydrogen peroxide was studied. The reaction was followed spectrophotometrically by measuring the absorbance of the reaction product at 360 nm. Under the optimum conditions 2 calibration graphs (for chromium(III) up to 100 ng mL-1, and for chromium(VI) up to 200 ng mL-1) were obtained, using the ``fixed time'' method with detection limits of 4.9 ng mL-1 and 3.8 ng mL-1, respectively...

  8. Perchlorate exposure in lactating women in an urban community in New Jersey

    International Nuclear Information System (INIS)

    Perchlorate is most widely known as a solid oxidant for missile and rocket propulsion systems although it is also present as a trace contaminant in some fertilizers. It has been detected in drinking water, fruits, and vegetables throughout New Jersey and most of the United States. At sufficiently high doses, perchlorate interferes with the uptake of iodine into the thyroid and may interfere with the development of the skeletal system and the central nervous system of infants. Therefore, it is important to quantify perchlorate in breast milk to understand potential perchlorate exposure in infants. In this study we measured perchlorate in breast milk, urine, and drinking water collected from 106 lactating mothers from Central New Jersey. Each subject was asked to provide three sets of samples over a 3-month period. The average ± SD perchlorate level in drinking water, breast milk, and urine was 0.168 ± 0.132 ng/mL (n = 253), 6.80 ± 8.76 ng/mL (n = 276), and 3.19 ± 3.64 ng/mL (3.51 ± 6.79 μg/g creatinine) (n = 273), respectively. Urinary perchlorate levels were lower than reference range values for women of reproductive age (5.16 ± 11.33 μg/g creatinine, p = 0.03), likely because of perchlorate secretion in breast milk. Drinking water perchlorate levels were ≤ 1.05 ng/mL and were not positively correlated with either breast milk or urine perchlorate levels. These findings together suggest that drinking water was not the most important perchlorate exposure source for these women. Creatinine-adjusted urine perchlorate levels were strongly correlated with breast milk perchlorate levels (r = 0.626, p = < 0.0005). Breast milk perchlorate levels in this study are consistent with widespread perchlorate exposure in lactating women and thus infants. This suggests that breast milk may be a source of exposure to perchlorate in infants. - Research Highlights: → The general population, including infants, is exposed to perchlorate. → Breast milk is a significant

  9. Inhibition of perchlorate reduction by nitrate in a fixed biofilm reactor

    International Nuclear Information System (INIS)

    Perchlorate and nitrate were reduced simultaneously in fixed biofilm reactors. Reduction of 1000 μg L-1 perchlorate decreased slightly with the addition of 10-16 mg L-1 NO3-N when excess acetate was supplied while denitrification was complete. When influent acetate was reduced by 50% to well below the stoichiometric requirement, perchlorate reduction decreased by 70% while denitrification decreased by only 20%, suggesting that competition for electrons by nitrate was a factor in inhibition. Reduction of nitrate was favored over perchlorate, even though reactor biofilm had been enriched under perchlorate-reducing conditions for 10 months. When excess acetate was restored, perchlorate and nitrate returned to initial levels. The average most probable numbers of perchlorate- and nitrate-reducing bacteria during excess substrate operation were not significantly different and ranged between 2.0 x 105 and 7.9 x 105 cells cm-2 media surface area. The effect of nitrate on chloride generation by suspensions of perchlorate-reducing populations was studied using a chloride ion probe. The rate of reduction of 2 mM perchlorate decreased by 30% in the presence of 2 mM nitrate when excess acetate was added. When acetate was limited, perchlorate reduction decreased by 70% in the presence of equi-molar nitrate

  10. Detection of Perchlorate Anion on Functionalized Silver Colloids Using Surface-Enhanced Raman Scattering

    Energy Technology Data Exchange (ETDEWEB)

    Tio, J.; Wang, W.; Gu, B.

    2005-01-01

    Perchlorate anion interferes with the uptake of iodide by the human thyroid gland and consequently disrupts the regulation of metabolism. Chronic exposure to high levels of perchlorate may lead to the formation of thyroid gland tumors. Although the Environmental Protection Agency (EPA) has not set a maximum contaminant level (MCL) for perchlorate, a draft drinking water range of 4-18 ppb based on 2 liter daily consumption of water has been established. The current EPA approved method for detecting perchlorate uses ion chromatography which has a detection limit of ~1ppb and involves lengthy analytical time in the laboratory. A unique combination of the surface-enhanced Raman scattering (SERS) effect and the bifunctional anion exchange resin’s high selectivity may provide an alternative way to detect perchlorate at such low concentrations and with high specificity. SERS, which uses laser excitation of adsorbed perchlorate anions on silver nanoparticles, has been shown to detect perchlorate anions at concentrations as low as 50 ppb. Normal micro-Raman analysis of perchlorate sorbed onto the resin beads has detected an even lower concentration of 10 ppb. In an effort to integrate these two effects, silver nanoparticles were coated with N-trimethoxysilylpropyl-N,N,N-trimethylammonium chloride, a functional group similar to that found on the resin bead, and subsequently inserted into different perchlorate concentration environments. This method has resulted in perchlorate detection down to ~10 ppb and a more consistent detection of perchlorate anion at ~50 ppb than that of earlier methods. As suggested by the direct insertion of functionalized silver colloids into perchlorate samples, this technique may potentially allow for the development of a probe using on-site Raman spectrometry to detect significantly low concentrations of perchlorate in situ rather than in the laboratory.

  11. Sensitivity and adaptability of methanogens to perchlorates: Implications for life on Mars

    Science.gov (United States)

    Kral, Timothy A.; Goodhart, Timothy H.; Harpool, Joshua D.; Hearnsberger, Christopher E.; McCracken, Graham L.; McSpadden, Stanley W.

    2016-01-01

    In 2008, the Mars Phoenix Lander discovered perchlorate at its landing site, and in 2012, the Curiosity rover confirmed the presence of perchlorate on Mars. The research reported here was designed to determine if certain methanogens could grow in the presence of three different perchlorate salt solutions. The methanogens tested were Methanothermobacter wolfeii, Methanosarcina barkeri, Methanobacterium formicicum and Methanococcus maripaludis. Media were prepared containing 0%, 0.5%, 1.0%, 2%, 5% and 10% wt/vol magnesium perchlorate, sodium perchlorate, or calcium perchlorate. Organisms were inoculated into their respective media followed by incubation at each organism's growth temperature. Methane production, commonly used to measure methanogen growth, was measured by gas chromatography of headspace gas samples. Methane concentrations varied with species and perchlorate salt tested. However, all four methanogens produced substantial levels of methane in the presence of up to 1.0% perchlorate, but not higher. The standard procedure for growing methanogens typically includes sodium sulfide, a reducing agent, to reduce residual molecular oxygen. However, the sodium sulfide may have been reducing the perchlorate, thus allowing for growth of the methanogens. To investigate this possibility, experiments were conducted where stainless steel nails were used instead of sodium sulfide as the reducing agent. Prior to the addition of perchlorate and inoculation, the nails were removed from the liquid medium. Just as in the prior experiments, the methanogens produced methane at comparable levels to those seen with sodium sulfide as the reductant, indicating that sodium sulfide did not reduce the perchlorate to any significant extent. Additionally, cells metabolizing in 1% perchlorate were transferred to 2%, cells metabolizing in 2% were transferred to 5%, and finally cells metabolizing in 5% were transferred to 10%. All four species produced methane at 2% and 5%, but not 10

  12. Relative source contributions for perchlorate exposures in a lactating human cohort

    Energy Technology Data Exchange (ETDEWEB)

    Kirk, Andrea B. [University of North Texas Health Sciences Center (United States); Dyke, Jason V. [University of Texas at Arlington (United States); Ohira, Shin-Ichi [Kumamoto University (Japan); Dasgupta, Purnendu K., E-mail: Dasgupta@uta.edu [University of Texas at Arlington (United States)

    2013-01-15

    Perchlorate is an iodine-uptake inhibitor and common contaminant of food and drinking water. Understanding the amount of perchlorate exposure occurring through non-water sources is essential for accurate estimates of human exposure levels, and establishment of drinking water limits for this pervasive contaminant. The study objective was to determine the amount of perchlorate intake derived from diet rather than water. Subjects provided drinking water samples, detailed fluid-intake records, 24 h urine collections and four milk samples for nine days. Samples were analyzed for perchlorate by isotope dilution ion chromatography–tandem mass spectrometry. Amounts of perchlorate derived from drinking water and dietary sources were calculated for each individual. Water of local origin was found to contribute a minor fraction of perchlorate intake. Estimated fraction intake from drinking water ranged from 0 to 36%. The mean and median dose of perchlorate derived from non-water sources by lactating women was 0.18 μg/kg/day (range: 0.06 to 0.36 μg/kg/day.) Lactating women consumed more fluid (mean 2.424 L/day) than has been assumed in recent risk assessments for perchlorate. The data reported here indicate that lactating women may be exposed to perchlorate through dietary sources at markedly higher levels than estimated previously. Exposures to perchlorate from non-water sources may be higher than recent estimates, including those used to develop drinking water standards. - Highlights: ► Residence in an area with perchlorate-contaminated water may be a poor predictor of exposure. ► Exposures to perchlorate from food are likely underestimated. ► The relative contributions for human perchlorate exposures should be weighted more heavily towards non-water sources.

  13. Relative source contributions for perchlorate exposures in a lactating human cohort

    International Nuclear Information System (INIS)

    Perchlorate is an iodine-uptake inhibitor and common contaminant of food and drinking water. Understanding the amount of perchlorate exposure occurring through non-water sources is essential for accurate estimates of human exposure levels, and establishment of drinking water limits for this pervasive contaminant. The study objective was to determine the amount of perchlorate intake derived from diet rather than water. Subjects provided drinking water samples, detailed fluid-intake records, 24 h urine collections and four milk samples for nine days. Samples were analyzed for perchlorate by isotope dilution ion chromatography–tandem mass spectrometry. Amounts of perchlorate derived from drinking water and dietary sources were calculated for each individual. Water of local origin was found to contribute a minor fraction of perchlorate intake. Estimated fraction intake from drinking water ranged from 0 to 36%. The mean and median dose of perchlorate derived from non-water sources by lactating women was 0.18 μg/kg/day (range: 0.06 to 0.36 μg/kg/day.) Lactating women consumed more fluid (mean 2.424 L/day) than has been assumed in recent risk assessments for perchlorate. The data reported here indicate that lactating women may be exposed to perchlorate through dietary sources at markedly higher levels than estimated previously. Exposures to perchlorate from non-water sources may be higher than recent estimates, including those used to develop drinking water standards. - Highlights: ► Residence in an area with perchlorate-contaminated water may be a poor predictor of exposure. ► Exposures to perchlorate from food are likely underestimated. ► The relative contributions for human perchlorate exposures should be weighted more heavily towards non-water sources

  14. CHROMIUM, METABOLIC SYNDROME AND DIABESITY

    Science.gov (United States)

    Suboptimal intakes of the essential nutrient, chromium, are characterized by elevated blood glucose, insulin resistance, obesity, hypertriglyceridemia, and low HDL. These are also signs and symptoms of the metabolic syndrome. Improvements due to increased intake of chromium are related to the degr...

  15. Groundwater contaminant by hexavalent chromium

    Energy Technology Data Exchange (ETDEWEB)

    Parsons, C. [Univ. of Texas, Austin, TX (United States)

    1995-11-01

    Oxidation of trivalent chromium to hexavalent chromium has been investigated as a function of total manganese in soils as well as various incubation conditions. Chromium and manganese contents were analyzed by atomic absorption (graphite furnace and flame emission respectively) following acid digestion. Total hexavalent chromium generation capacity was determined by addition of 0.001 M CrCL3, incubation, and analysis by s-diphenyl carbazide. Samples were then leached with CaSO{sub 4} and MgSO{sub 4} and incubated in various environments (oven, freeze-drier, field moist, ultrafreeze) to test for geogenic generation of Cr(IV). The degree of geogenic generation of hexavalent chromium was compared with total Mn and Cr content as well as hexavalent generational capacity.

  16. Isotopic tracing of perchlorate sources in groundwater from Pomona, California

    International Nuclear Information System (INIS)

    Highlights: • Isotopic analysis of groundwater perchlorate can provide source identification. • Citrus cultivation in Pomona, CA caused perchlorate contamination of groundwater. • Hydrologic modeling and mass balance support interpretation of perchlorate source. - Abstract: The groundwater of Pomona, California, is contaminated with perchlorate (ClO4-). This water is treated to reduce the ClO4- concentration to less than 6 μg L−1 for compliance with California Department of Public Health drinking water regulations. A study of the isotopic composition of oxygen and chlorine in ClO4- has been conducted to determine the source of the contamination. Isotopic compositions were measured for ClO4- samples extracted from 14 wells, yielding ranges of δ18O values from −10.8‰ to −8.0‰, Δ17O values from +4.6‰ to +7.5‰, and δ37Cl values from −12.8‰ to −8.9‰. Evaluation of mixing proportions using published isotopic data for three ClO4- end-members (synthetic, Atacama, and indigenous natural ClO4-) indicates that contamination is dominantly (85–89%) Atacama ClO4- derived from past use of imported Chilean nitrate fertilizer in citrus cultivation. This interpretation is consistent with (1) aerial photography archives showing extensive citrus fields surrounding Pomona in the early- to mid-20th century, (2) mass-balance estimates for ClO4-, and (3) numerical hydrologic models yielding travel-times for ClO4- from fields to wells that are in the range of 15 to >100 years. The hydrologic models predict that ClO4- contamination of Pomona groundwater will persist for decades into the future

  17. 4-(2-Azaniumylethylpiperazin-1-ium bis(perchlorate

    Directory of Open Access Journals (Sweden)

    Mohammad Reza Reisi

    2011-09-01

    Full Text Available In the title compound, C6H17N32+·2ClO4−, the piperazine ring adopts a chair conformation with the ethylammonium fragment occupying an equatorial position. In the crystal, the dications and perchlorate anions are linked through N—H...O hydrogen bonding and weak C—H...O hydrogen bonding into a three-dimensional supramolecular network.

  18. Genetic Factors That Might Lead to Different Responses in Individuals Exposed to Perchlorate

    OpenAIRE

    Scinicariello, Franco; Murray, H. Edward; Smith, Lester; Wilbur, Sharon; Fowler, Bruce A.

    2005-01-01

    Perchlorate has been detected in groundwater in many parts of the United States, and recent detection in vegetable and dairy food products indicates that contamination by perchlorate is more widespread than previously thought. Perchlorate is a competitive inhibitor of the sodium iodide symporter, the thyroid cell–surface protein responsible for transporting iodide from the plasma into the thyroid. An estimated 4.3% of the U.S. population is subclinically hypothyroid, and 6.9% of pregnant wome...

  19. Purification and Characterization of (Per)Chlorate Reductase from the Chlorate-Respiring Strain GR-1

    OpenAIRE

    Kengen, Servé W. M.; Rikken, Geoffrey B.; Hagen, Wilfred R.; van Ginkel, Cees G.; Stams, Alfons J. M.

    1999-01-01

    Strain GR-1 is one of several recently isolated bacterial species that are able to respire by using chlorate or perchlorate as the terminal electron acceptor. The organism performs a complete reduction of chlorate or perchlorate to chloride and oxygen, with the intermediate formation of chlorite. This study describes the purification and characterization of the key enzyme of the reductive pathway, the chlorate and perchlorate reductase. A single enzyme was found to catalyze both the chlorate-...

  20. Transposon and Deletion Mutagenesis of Genes Involved in Perchlorate Reduction in Azospira suillum PS

    OpenAIRE

    Melnyk, Ryan A.; Clark, Iain C.; Liao, Annette; Coates, John D.

    2013-01-01

    ABSTRACT Although much work on the biochemistry of the key enzymes of bacterial perchlorate reduction, chlorite dismutase, and perchlorate reductase has been published, understanding of the molecular mechanisms of this metabolism has been somewhat hampered by the lack of a clear model system amenable to genetic manipulation. Using transposon mutagenesis and clean deletions, genes important for perchlorate reduction in Azospira suillum PS have been identified both inside and outside the previo...

  1. Extraction of scandium ions by 1-alkyl-3-methyl-2-pyrazoline-5-ones from perchlorate solutions

    International Nuclear Information System (INIS)

    Extraction of acid and interphase distribution of 1-alkyl-3-methyl-2-pyrazoline-5-ones in the system water-chloroform-perchloric acid are studied. Reagents capable to extract scandium cations from subacid solutions in the presence of perchlorate ions. 1-Alkyl-3-methyl-2-pyrazoline-5-ones stratifies aqueous solutions of perchloric acid into two liquid phase. Scandium ions are concentrated in the lower phase having small volume

  2. Role of paramagnetic chromium in chromium(VI)-induced damage in cultured mammalian cells.

    OpenAIRE

    Sugiyama, M

    1994-01-01

    Chromium(VI) compounds are known to be potent toxic and carcinogenic agents. Because chromium(VI) is easily taken up by cells and is subsequently reduced to chromium(III), the formation of paramagnetic chromium such as chromium(V) and chromium(III) is believed to play a role in the adverse biological effects of chromium(VI) compounds. The present report, uses electron spin resonance (ESR) spectroscopy; the importance of the role of paramagnetic chromium in chromium(VI)-induced damage in intac...

  3. Uranyl ion behaviour in perchloric media and its extraction by TBP CCl/sub 4/

    Energy Technology Data Exchange (ETDEWEB)

    Yahia, A. (Centre de Developpement des Materiaux, Commissariat aux Energies Nouvelles, Alger (Algeria)); Benali-Baitich, O. (Universite des Sciences et de la Technologie Houari Boumediene (USTHB), Institut de Chimie, Alger (Algeria))

    The behaviour of uranyl ion in aqueous solution of perchloric acid (O < Cub(HC104) < 13 mol.1/sup -1/) shows that for an acidity higher than 9 mol.1/sup -1/, there is formation of a monoperchlorato complex. The extraction of uranly perchlorate from aqueous perchloric solutions by TBP diluted CC1/sub 4/ as a function of uranium and perchloric acid concentrations enabled us on one hand, to concluded that UO/sub 2//sup + +/ is solvated by 2 TBP molecules, and on the other hand, to determine the composition of the coextracted HC1O/sub 4/ solvated species.

  4. Perchlorate in fish from a contaminated site in east-central Texas

    International Nuclear Information System (INIS)

    Perchlorate, a known thyroid endocrine disruptor, contaminates surface waters near military instillations where solid fuel rocket motors are manufactured or assembled. To assess potential perchlorate exposure to fish and the human population which may feed on them, fish were collected around the Naval Weapons Industrial Reserve Plant in McLennan County, TX, and analyzed for the presence of the perchlorate anion. The sampling sites included Lake Waco and Belton Lake, and several streams and rivers within their watersheds. The general tendency was that perchlorate was only found in a few species sampled, and perchlorate was not detected in every individual within these species. When detected in the fish, perchlorate tissue concentrations were greater than that in the water. This may be due to highly variable perchlorate concentrations in the water coupled with individual-level variation in elimination from the body, or to routes of exposure other than water. - In perchlorate-contaminated lakes and streams, perchlorate is detected infrequently in fish heads, fillets, and whole bodies, but may be detected more often depending on species and seasonal trends, and always at concentrations higher in the fish than in the water

  5. Containerized Wetland Bioreactor Evaluated for Perchlorate and Nitrate Degradation

    Energy Technology Data Exchange (ETDEWEB)

    Dibley, V R; Krauter, P W

    2004-12-02

    The U.S. Department of Energy (DOE) and Lawrence Livermore Laboratory (LLNL) designed and constructed an innovative containerized wetlands (bioreactor) system that began operation in November 2000 to biologically degrade perchlorate and nitrate under relatively low-flow conditions at a remote location at Site 300 known as Building 854. Since initial start-up, the system has processed over 3,463,000 liters of ground water and treated over 38 grams of perchlorate and 148 kilograms of nitrate. Site 300 is operated by the University of California as a high-explosives and materials testing facility supporting nuclear weapons research. The 11-square mile site located in northern California was added to the NPL in 1990 primarily due to the presence of elevated concentrations of volatile organic compounds (VOCs) in ground water. At the urging of the regulatory agencies, perchlorate was looked for and detected in the ground water in 1999. VOCs, nitrate and perchlorate were released into the soil and ground water in the Building 854 area as the result of accidental leaks during stability testing of weapons or from waste discharge practices that are no longer permitted at Site 300. Design of the wetland bioreactors was based on earlier studies showing that indigenous chlorate-respiring bacteria could effectively degrade perchlorate into nontoxic concentrations of chlorate, chlorite, oxygen, and chloride. Studies also showed that the addition of organic carbon would enhance microbial denitrification. Early onsite testing showed acetic acid to be a more effective carbon source than dried leaf matter, dried algae, or milk replacement starter; a nutrient and carbon source used in a Department of Defense phytoremediation demonstration. No inocula were added to the system. Groundwater was allowed to circulate through the bioreactor for three weeks to acclimate the wetland plants and to build a biofilm from indigenous flora. Using solar energy, ground water is pumped into granular

  6. Fate and transport of chromium through soil

    International Nuclear Information System (INIS)

    Chromium chemistry relevant to the problem facing state of New Jersey (Usa) was examined. Transport of chromium through soil depends on its chemical forms. Transformation of chromium within bulk of soil depends on soil constituents, soil condition, such as pH, Eh and organic compounds applied onto soil or present in soil. Total chromium in soil can be determined. Speciation of chromium based on ionization, hydrolysis, complex formation, redox reactions and adsorption is predicted using MINIQ program

  7. Release of Chromium from Orthopaedic Arthroplasties

    OpenAIRE

    Afolaranmi, G.A.; Tettey, J; Meek, R.M.D; Grant, M.H

    2008-01-01

    Many orthopaedic implants are composed of alloys containing chromium. Of particular relevance is the increasing number of Cobalt Chromium bearing arthroplasies being inserted into young patients with osteoarthritis. Such implants will release chromium ions. These patients will be exposed to the released chromium for over 50 years in some cases. The subsequent chromium ion metabolism and redistribution in fluid and tissue compartments is complex. In addition, the potential biological effects o...

  8. Chromium isotope variations

    DEFF Research Database (Denmark)

    D'Arcy, Joan Mary

    Chromium (Cr) stable isotopes are a useful tracer of changes in redox conditions because changes in its oxidation state are accompanied by an isotopic fractionation. For this reason the Cr isotope system is being developed as a potential tool for paleo-redox reconstruction. Dissolved Cr in seawater...... is incorporated into carbonates. Hence, ancient carbonates can potentially record the Cr isotopic composition (δ53Cr ‰) of seawater in the geological past. Reliable application and interpretation of this proxy requires a detailed knowledge about processes that fractionate Cr on the Earth’s surface......, and the quantification the Cr isotope composition of major Cr fluxes into and out of ocean. This thesis adds to the current knowledge of the Cr isotope system and is divided into two studies. The focus of the first study was to determine what processes control the Cr isotopic compositionof river...

  9. Perchlorate in the Hydrologic Cycle - An Overview of Sources and Occurrence

    Science.gov (United States)

    Stonestrom, D. A.; Jackson, W.; Mayer, K.; Orris, G. J.

    2007-12-01

    Perchlorate (ClO4-) in water and food is of concern due to deleterious health affects associated with hypothyroidism. The presence of widespread perchlorate in 0-to-28 ka-old pristine ground water of the Middle Rio Grande Basin (Plummer et al., 2006, ES&T, DOI:10.1021/es051739h), in ground water >1 mile from agricultural activities in the Southern High Plains (Rajagapolan et al., 2006, ES&T, DOI:10.1021/es052155i), and in unsaturated zones throughout the arid and semiarid southwestern United States (Rao et al., 2007, ES&T, DOI:10.1021/es062853i) clearly indicates that perchlorate is a non-exotic component of the hydrologic cycle, at least in dry environments. The natural system has been greatly perturbed in places by human activities. Most anthropogenic inputs are associated with the manufacture and use of explosives and rocket fuel, providing concentrated sources of excess perchlorate to the hydrologic cycle. Perchlorate-containing fertilizers and irrigation provide dispersed sources within and down-gradient from agricultural areas. Natural sources include photochemically mediated reactions involving ozone at the land surface and in the lower atmosphere. A growing body of work indicates that a small, but persistent, meteoric source acting over thousands of years can explain observed accumulations of unsaturated-zone perchlorate in arid regions. In addition to meteoric sources, oxyanions produced during volcanogenic processes can include appreciable amounts of natural perchlorate. Terrestrial plants take up perchlorate in soil water, with some species of xerophytic succulents concentrating the anion to high levels. Similarly, perchlorate in marine plants indicates that perchlorate is part of marine biochemical cycles. Perchlorate-bearing marine sediments of late Tertiary age suggest that perchlorate has been part of global geochemical cycles for millions of years and, furthermore, can be preserved in the subsurface despite the nearly ubiquitous presence of

  10. Physiological and Genetic Description of Dissimilatory Perchlorate Reduction by the Novel Marine Bacterium Arcobacter sp. Strain CAB

    OpenAIRE

    Carlström, Charlotte I.; Wang, Ouwei; Melnyk, Ryan A.; Bauer, Stefan; Lee, Joyce; Engelbrektson, Anna; Coates, John D.

    2013-01-01

    ABSTRACT A novel dissimilatory perchlorate-reducing bacterium (DPRB), Arcobacter sp. strain CAB, was isolated from a marina in Berkeley, CA. Phylogenetically, this halophile was most closely related to Arcobacter defluvii strain SW30-2 and Arcobacter ellisii. With acetate as the electron donor, strain CAB completely reduced perchlorate (ClO4 −) or chlorate (ClO3 −) [collectively designated (per)chlorate] to innocuous chloride (Cl−), likely using the perchlorate reductase (Pcr) and chlorite di...

  11. Chromium reduction in Pseudomonas putida.

    OpenAIRE

    Ishibashi, Y.; Cervantes, C; Silver, S

    1990-01-01

    Reduction of hexavalent chromium (chromate) to less-toxic trivalent chromium was studied by using cell suspensions and cell-free supernatant fluids from Pseudomonas putida PRS2000. Chromate reductase activity was associated with soluble protein and not with the membrane fraction. The crude enzyme activity was heat labile and showed a Km of 40 microM CrO4(2-). Neither sulfate nor nitrate affected chromate reduction either in vitro or with intact cells.

  12. Chromium reduction in Pseudomonas putida.

    Science.gov (United States)

    Ishibashi, Y; Cervantes, C; Silver, S

    1990-01-01

    Reduction of hexavalent chromium (chromate) to less-toxic trivalent chromium was studied by using cell suspensions and cell-free supernatant fluids from Pseudomonas putida PRS2000. Chromate reductase activity was associated with soluble protein and not with the membrane fraction. The crude enzyme activity was heat labile and showed a Km of 40 microM CrO4(2-). Neither sulfate nor nitrate affected chromate reduction either in vitro or with intact cells. PMID:2389940

  13. Bifunctional lanthanum phosphate substrates as novel adsorbents and biocatalyst supports for perchlorate removal

    Energy Technology Data Exchange (ETDEWEB)

    Sankar, Sasidharan [Materials Science and Technology Division (India); Prajeesh, Gangadharan Puthiya Veetil; Anupama, Vijaya Nadaraja [Process Engineering and Environmental Technology Division, CSIR – National Institute for Interdisciplinary Science and Technology, Industrial Estate P.O., Thiruvananthapuram 695019 (India); Krishnakumar, Bhaskaran [Process Engineering and Environmental Technology Division, CSIR – National Institute for Interdisciplinary Science and Technology, Industrial Estate P.O., Thiruvananthapuram 695019 (India); Academy of Scientific and Industrial Research (AcSIR) (India); Hareesh, Padinhattayil [Materials Science and Technology Division (India); Nair, Balagopal N. [R and D Centre, Noritake Co. Ltd., Aichi (Japan); Warrier, Krishna Gopakumar [Materials Science and Technology Division (India); Academy of Scientific and Industrial Research (AcSIR) (India); Hareesh, Unnikrishnan Nair Saraswathy, E-mail: hareesh@niist.res.in [Materials Science and Technology Division (India); Academy of Scientific and Industrial Research (AcSIR) (India)

    2014-06-30

    Graphical abstract: Porous lanthanum phosphate substrates, obtained by an environmentally benign thermal gelation process, performed the role of dual functional sorbent facilitating perchlorate adsorption and bioremediation through the growth of perchlorate reducing microbial colonies. - Highlights: • Lanthanum phosphate monoliths as efficient perchlorate adsorbents. • And also as substrates for biofilm (perchlorate reducing bacteria) growth. • Environmentally benign thermal gelation process for substrate fabrication. • 98% adsorption efficiency for perchlorate concentrations up to 100 μg/L. • The regenerated monoliths show nearly 100% reusability. - Abstract: Porous lanthanum phosphate substrates, obtained by an environmentally benign colloidal forming process employing methyl cellulose, are reported here as excellent adsorbents of perchlorate with >98% efficiency and with 100% reusability. Additionally, the effectiveness of such substrates as biocatalyst supports that facilitate biofilm formation of perchlorate reducing microbes (Serratia marcescens NIIST 5) is also demonstrated for the first time. The adsorption of perchlorate ions is attributed to the pore structure of lanthanum phosphate substrate and the microbial attachment is primarily ascribed to its intrinsic hydrophobic property. Lanthanum phosphate thus emerges as a dual functional material that possesses an integrated adsorption/bioremediation property for the effective removal of ClO{sub 4}{sup −} which is an increasingly important environmental contaminant.

  14. Identification of a Perchlorate Reduction Genomic Island with Novel Regulatory and Metabolic Genes ▿

    OpenAIRE

    Melnyk, Ryan A.; Engelbrektson, Anna; Clark, Iain C.; Carlson, Hans K.; Byrne-Bailey, Kathy; Coates, John D.

    2011-01-01

    A comparative analysis of the genomes of four dissimilatory (per)chlorate-reducing bacteria has revealed a genomic island associated with perchlorate reduction. In addition to the characterized metabolic genes for perchlorate reductase and chlorite dismutase, the island contains multiple conserved uncharacterized genes possibly involved in electron transport and regulation.

  15. Identification of a perchlorate reduction genomic island with novel regulatory and metabolic genes.

    Science.gov (United States)

    Melnyk, Ryan A; Engelbrektson, Anna; Clark, Iain C; Carlson, Hans K; Byrne-Bailey, Kathy; Coates, John D

    2011-10-01

    A comparative analysis of the genomes of four dissimilatory (per)chlorate-reducing bacteria has revealed a genomic island associated with perchlorate reduction. In addition to the characterized metabolic genes for perchlorate reductase and chlorite dismutase, the island contains multiple conserved uncharacterized genes possibly involved in electron transport and regulation. PMID:21856823

  16. Bifunctional lanthanum phosphate substrates as novel adsorbents and biocatalyst supports for perchlorate removal

    International Nuclear Information System (INIS)

    Graphical abstract: Porous lanthanum phosphate substrates, obtained by an environmentally benign thermal gelation process, performed the role of dual functional sorbent facilitating perchlorate adsorption and bioremediation through the growth of perchlorate reducing microbial colonies. - Highlights: • Lanthanum phosphate monoliths as efficient perchlorate adsorbents. • And also as substrates for biofilm (perchlorate reducing bacteria) growth. • Environmentally benign thermal gelation process for substrate fabrication. • 98% adsorption efficiency for perchlorate concentrations up to 100 μg/L. • The regenerated monoliths show nearly 100% reusability. - Abstract: Porous lanthanum phosphate substrates, obtained by an environmentally benign colloidal forming process employing methyl cellulose, are reported here as excellent adsorbents of perchlorate with >98% efficiency and with 100% reusability. Additionally, the effectiveness of such substrates as biocatalyst supports that facilitate biofilm formation of perchlorate reducing microbes (Serratia marcescens NIIST 5) is also demonstrated for the first time. The adsorption of perchlorate ions is attributed to the pore structure of lanthanum phosphate substrate and the microbial attachment is primarily ascribed to its intrinsic hydrophobic property. Lanthanum phosphate thus emerges as a dual functional material that possesses an integrated adsorption/bioremediation property for the effective removal of ClO4− which is an increasingly important environmental contaminant

  17. Terbium nitrate luminescence quenching by eosin in he presence of lithium perchlorate in sulfolane solutions

    International Nuclear Information System (INIS)

    Quenching of terbium nitrate luminescence by anionic dye, eosin, in the presence of lithium perchlorate in sulfolane solutions was studied. Temperature dependence of terbium nitrate luminescence in sulfolane solutions in the presence of perchlorate anions were considered. The values of energy required for water molecular substitution in Tb3+ ion coordination sphere for solvent molecule in electrolyte solution were ascertained

  18. Archaeal (Per)Chlorate Reduction at High Temperature: An Interplay of Biotic and Abiotic Reactions

    NARCIS (Netherlands)

    Liebensteiner, M.; Pinkse, M.W.H.; Schaap, P.J.; Stams, A.J.M.; Lomans, B.P.

    2013-01-01

    Perchlorate and chlorate anions [(per)chlorate] exist in the environment from natural and anthropogenic sources, where they can serve as electron acceptors for bacteria. We performed growth experiments combined with genomic and proteomic analyses of the hyperthermophile Archaeoglobus fulgidus that s

  19. Monitoring of perchlorate in diverse foods and its estimated dietary exposure for Korea populations.

    Science.gov (United States)

    Lee, Ji-Woo; Oh, Sung-Hee; Oh, Jeong-Eun

    2012-12-01

    The perchlorate concentrations in various Korean food samples were monitored, and 663 samples belonging to 39 kinds of food were analyzed. The analysis results revealed that dairy products contain the highest average concentration of 6.34 μg/kg and high detection frequency of over 85%. Fruit and vegetables showed the next highest perchlorate concentration with an average of 6.17 μg/kg. Especially, with its average concentration of 39.9 μg/kg, spinach showed the highest perchlorate level among all target food samples studied. Tomato was followed by spinach, which showed a high perchlorate average concentration of 19.8 μg/kg, and over 7 μg/kg was detected in ham and sausage (avg. 7.31 μg/kg) and in instant noodles (avg. 7.58 μg/kg). Less than 2 μg/kg was detected in fishes, meats and beverages. The exposure dose of perchlorate in Korean by food intake was calculated on the basis of the analyzed perchlorate levels in this study. The daily perchlorate dose to which Korean adults are exposed is 0.04 μg/kg bw/day, which is lower than the RfD (0.7 μg/kg bw/day) value suggested by US NAS. This result indicates that Korean people's current exposure to perchlorate from domestic food consumption is evaluated as safe. PMID:23116718

  20. Photodimerization and photooxygenation of 9-vinylcarbazole catalyzed by titanium dioxide and magnesium perchlorate

    Institute of Scientific and Technical Information of China (English)

    Hajime; Maeda; Mio; Yamamoto; Hideyuki; Nakagawa; Kazuhiko; Mizuno

    2010-01-01

    Photoreaction of 9-vinylcarbazole in acetonitrile in the presence of titanium dioxide and a catalytic amount of magnesium perchlorate gave 3,6-di(9-carbazolyl)-1,2-dioxane as a photooxygenated product via photodimerization of 9-vinylcarbazole.The photoreaction proceeds via an electron transfer mechanism,where magnesium perchlorate accelerated formation of the photo-oxygenated product.

  1. CRYSTALLIZATION KINETICS OF AMMONIUM PERCHLORATE IN AN AGITATED VESSEL

    Directory of Open Access Journals (Sweden)

    Nahidh Kaseer

    2013-05-01

    Full Text Available 31Overall crystal growth kinetics for ammonium perchlorate in laboratory scale batch  agitated vessel crystallizer have been determined from batch experiments performed in an integral mode. The effects of temperature between 30-60ºC, seed size 0.07, 0.120 and 0.275 mm and stirrer speed 160, 340, and 480 rpm, on the kinetics of crystal growth were investigated. Two different methods, viz. polynomial fitting and initial derivative were used to predict the kinetics expression. In general both methods gave comparable results for growth kinetics estimation. The order of growth process is not more than two. The activation energy for crystal growth of ammonium perchlorate was determined and found  to be equal to 5.8 kJ/ mole.            Finally, the influence of the affecting parameters on the crystal growth rate gives general expression that had an obvious dependence of the growth rate on each variables of concern (temperature, seed size, and stirrer speed .The general overall growth rate expression had shown that super saturation is the most significant variable. While the positive dependence of the stirrer speed demonstrates the importance of the diffusional step in the growth rate model. Moreover, the positive dependence of the seed size demonstrate the importance of the surface integration  step in the growth rate model. All the studied variables tend to suggest that the growth rate characteristics  of ammonium perchlorate from aqueous solution commenced in a batch crystallizer are diffusion kinetic controlled process.

  2. (Dicyanamido)[tris(2-pyridylmethyl)amine]zinc(II) perchlorate

    OpenAIRE

    Shi Guo Zhang; Hong Yan Zhao; Hong Li

    2008-01-01

    In the title complex, [Zn(C2N3)(C18H18N4)]ClO4, the ZnII ion has a slightly distorted trigonal–bipyramidal ZnN5 coordination geometry. The crystal structure is stabilized by weak intermolecular C—H...O and C—H...N hydrogen bonds. In addition, there are relatively close contacts between the O atoms of the perchlorate anion and symmetry-related pyridine rings [O...Cg = 3.179 (3) and 3.236 (3) Å, where Cg is the centroid of a pyridine ring], and between t...

  3. CRYSTALLIZATION KINETICS OF AMMONIUM PERCHLORATE IN AN AGITATED VESSEL

    OpenAIRE

    Nahidh Kaseer; Rafi' J. Yaqub; Ahmed Khalid

    2013-01-01

    31Overall crystal growth kinetics for ammonium perchlorate in laboratory scale batch  agitated vessel crystallizer have been determined from batch experiments performed in an integral mode. The effects of temperature between 30-60ºC, seed size 0.07, 0.120 and 0.275 mm and stirrer speed 160, 340, and 480 rpm, on the kinetics of crystal growth were investigated. Two different methods, viz. polynomial fitting and initial derivative were used to predict the kinetics expression. In general both me...

  4. Prediction of Particle Size of Ammonium Perchlorate during Pulverisation

    Directory of Open Access Journals (Sweden)

    Sunil Jain

    2006-07-01

    Full Text Available Ammonium perchlorate has been pulverised by an impact mill (air classifier mill to studythe influence of different operating parameters, viz., effect of mill speed, classifier speed, feedrate, and damper opening (suction rate on the particle size. Further based on the differentgrinding parameters, an empirical equation has been developed and used for the prediction ofparticle size. The experimental results indicate that the values are very close to the predictedones. In addition, particle size distribution has also been studied by applying different modelequations and it has been found that Rosin-Rammler model is the most suitable model for thisoperation.

  5. Comparative DFT study of crystalline ammonium perchlorate and ammonium dinitramide.

    Science.gov (United States)

    Zhu, Weihua; Wei, Tao; Zhu, Wei; Xiao, Heming

    2008-05-22

    The electronic structure, vibrational properties, absorption spectra, and thermodynamic properties of crystalline ammonium perchlorate (AP) and ammonium dinitramide (ADN) have been comparatively studied using density functional theory in the local density approximation. The results shows that the p states for the two solids play a very important role in their chemical reaction. From the low frequency to high frequency region, ADN has more motion modes for the vibrational frequencies than AP. The absorption spectra of AP and ADN display a few, strong bands in the fundamental absorption region. The thermodynamic properties show that ADN is easier to decompose than AP as the temperature increases. PMID:18396853

  6. Specific heat and thermodynamic properties of the cesium perchlorate

    International Nuclear Information System (INIS)

    The cesium perchlorate specific heat has been measured in a vacuum adiabatic microcalorimeter in the 10-365 K range. On the basis of the data obtained the thermodynamic functions are calculated. Csub(p)sup(0) (298.15 K) = 110.4+-0.2 J/Kxmol; S0 (298.15 K)=175.9+-0.5 J/Kxmol; H0 (298.15 K) - H0(0)=22280+-50 J/mol; - [G0 (289.15 K) - H0(0)]/T = 101.2+-0.2 J/Kxmol

  7. Detoxification of PAX-21 ammunitions wastewater by zero-valent iron for microbial reduction of perchlorate.

    Science.gov (United States)

    Ahn, Se Chang; Cha, Daniel K; Kim, Byung J; Oh, Seok-Young

    2011-08-30

    US Army and the Department of Defense (DoD) facilities generate perchlorate (ClO(4)(-)) from munitions manufacturing and demilitarization processes. Ammonium perchlorate is one of the main constituents in Army's new main charge melt-pour energetic, PAX-21. In addition to ammonium perchlorate, hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) and 2,4-dinitroanisole (DNAN) are the major constituents of PAX-21. In order to evaluate microbial perchlorate reduction as a practical option for the treatment of perchlorate in PAX-21 wastewater, we conducted biodegradation experiments using glucose as the primary sources of electrons and carbon. Batch experiments showed that negligible perchlorate was removed in microbial reactors containing PAX-21 wastewater while control bottles containing seed bacteria and glucose rapidly and completely removed perchlorate. These results suggested that the constituents in PAX-21 wastewater may be toxic to perchlorate reducing bacteria. A series of batch toxicity test was conducted to identify the toxic constituents in PAX-21 and DNAN was identified as the primary toxicant responsible for inhibiting the activity of perchlorate reducing bacteria. It was hypothesized that pretreatment of PAX-21 by zero-valent iron granules will transform toxic constituents in PAX-21 wastewater to non-toxic products. We observed complete reduction of DNAN to 2,4-diaminoanisole (DAAN) and RDX to formaldehyde in abiotic iron reduction study. After a 3-day acclimation period, perchlorate in iron-treated PAX-21 wastewater was rapidly decreased to an undetectable level in 2 days. This result demonstrated that iron treatment not only removed energetic compounds but also eliminated the toxic constituents that inhibited the subsequent microbial process. PMID:21700387

  8. Characterization of Perchlorate in a New Frozen Human Urine Standard Reference Material

    Science.gov (United States)

    Yu, Lee L.; Jarrett, Jeffery M.; Davis, W. Clay; Kilpatrick, Eric L.; Oflaz, Rabia; Turk, Gregory C.; Leber, Dennis D.; Valentin, Liza; Morel-Espinosa, Maria; Blount, Benjamin C.

    2015-01-01

    Perchlorate, an inorganic anion, has recently been recognized as an environmental contaminant by the U.S. Environmental Protection Agency (EPA). Urine is the preferred matrix for assessment of human exposure to perchlorate. Although the measurement technique for perchlorate in urine was developed in 2005, the calibration and quality assurance aspects of the metrology infrastructure for perchlorate are still lacking in that there is no certified reference material (CRM) traceable to the International System of Units (SI). To meet the quality assurance needs in biomonitoring measurements of perchlorate and the related anions that affect thyroid health, the National Institute of Standards and Technology (NIST) in collaboration with the Centers for Disease Control and Prevention (CDC) developed Standard Reference Material (SRM) 3668 Mercury, Perchlorate, and Iodide in Frozen Human Urine. SRM 3668 consists of perchlorate, nitrate, thiocyanate, iodine, and mercury in urine at two levels that represent the 50th and 95th percentiles, respectively, of the concentrations (with some adjustments) in the U.S. population. It is the first CRM being certified for perchlorate. Measurements leading to the certification of perchlorate were made collaboratively at NIST and CDC using three methods based on liquid or ion chromatography tandem mass spectrometry (LC-MS/MS or IC-MS/MS). Potential sources of bias were analyzed and results were compared for the three methods. Perchlorate in SRM 3668 Level I urine was certified to be 2.70 μg L−1 ± 0.21 μg L−1, and for SRM 3668 Level II urine, the certified value is 13.47 μg L−1 ± 0.96 μg L−1. PMID:22850897

  9. Specific adsorption of perchlorate anions on Pt{hkl} single crystal electrodes.

    Science.gov (United States)

    Attard, Gary A; Brew, Ashley; Hunter, Katherine; Sharman, Jonathan; Wright, Edward

    2014-07-21

    The voltammetry of Pt{111}, Pt{100}, Pt{110} and Pt{311} single crystal electrodes as a function of perchloric acid concentration (0.05-2.00 M) has been studied in order to test the assertion made in recent reports by Watanabe et al. that perchlorate anions specifically adsorb on polycrystalline platinum. Such an assertion would have significant ramifications for our understanding of electrocatalytic processes at platinum surfaces since perchlorate anions at low pH have classically been assumed not to specifically adsorb. For Pt{111}, it is found that OHad and electrochemical oxide states are both perturbed significantly as perchloric acid concentration is increased. We suggest that this is due to specific adsorption of perchlorate anions competing with OHad for adsorption sites. The hydrogen underpotential deposition (H UPD) region of Pt{111} however remains unchanged although evidence for perchlorate anion decomposition to chloride on Pt{111} is reported. In contrast, for Pt{100} no variation in the onset of electrochemical oxide formation is found nor any shift in the potential of the OHad state which normally results from the action of specifically adsorbing anions. This suggests that perchlorate anions are non-specifically adsorbed on this plane although strong changes in all H UPD states are observed as perchloric acid concentration is increased. This manifests itself as a redistribution of charge from the H UPD state situated at more positive potential to the one at more negative potential. For Pt{110} and Pt{311}, marginal changes in the onset of electrochemical oxide formation are recorded, associated with specific adsorption of perchlorate. Specific adsorption of perchlorate anions on Pt{111} is deleterious to electrocatalytic activity in relation to the oxygen reduction reaction (ORR) as measured using a rotating disc electrode (RDE) in a hanging meniscus configuration. This study supports previous work suggesting that a large component of the ORR

  10. Hydrogen permeation through chromium

    International Nuclear Information System (INIS)

    Steady state and non-steady state measurements of hydrogen permeation through metallic chromium are reported. The experiments have been conducted by use of hydrogen and deuterium within a pressure range of 10-8 - 1 bar and temperatures between 600 - 8000C. Numerical values for the physical quantities permeability, diffusion constant and solubility could be derived. At an upstream pressure above around 10-3 bar classical Sieverts-low was found (permeation rate proportional √p) with activation energies Qsub(perm) = 65 kJoule/mole, Qsub(Diff) = 4-8 kJoule/mole, Qsub(Sol) = 57-61 kJoule/mole for the respective processes involved. The isotopic effect between H and D of the permeabilities could be represented by a factor of 1,5 independence on temperature. All non steady-state measurements could be approximated reasonably well by classical diffusion kinetics. Below up-stream pressures of approx.= 10-7 bar the kinetics was no longer diffusion controlled, the dependence on up-stream pressure changed from √p -> p, the activation energy for permetation increased to 127 kJoule/mole and the isotopic factor resulted in about 2-3. (orig.)

  11. Ion Chromatographic Determination of low level Perchlorate in Natural Waters

    International Nuclear Information System (INIS)

    Perchlorate (ClO4-) is a persistent contaminant of drinking-, surface-, and ground-water, and of soils. Possible contributions of ClO4- contamination are the military, the space program, and supporting industries and fertilizers. Perchlorate has long been known to have a negative effect on the thyroid gland. It has been added to the United States Environmental Protection Agency's (EPA) Contaminant candidate List (CCL) in 1998, so that ClO4 can be regulated at a concentration safe to humans. This paper describes the determination of trace level ClO4- in various matrices utilizing ion chromatographic method. The method utilizes a Dionex IonPac AS11 column with suppressed conductivity detection, 1500ul sample loop, and a 100 mN NaOH eluent at a flow rate of 1.0ml/min. These parameters allow a method detection limit (MDL) of 0.277ug/1 and a short retention time of 8 minutes. A quality control, proficiency testing samples from the EPA and a number of environmental samples from New York State (ground water) and California (ground and surface waters) were analyzed by this technique. Concentrations measured were in the range of 1.9-217 ug/1. No evidence of ClO4- was found in various commonly used fertilizers. (author)

  12. Extraction of scandium by benzoylantipyrine from chloride-perchlorate solutions

    International Nuclear Information System (INIS)

    Distribution of scandium complexes in case of extraction by benzoyl-4-antipyrine (BANT) in chloroform from aqueous chloride-perchlorate solutions, depending on extraction, perchlorate-ion and salting out agents concentration, was studied. It has been ascertained that scandium distribution factor is nearly 50 at NaClO4 and BANT concentrations equal to 2 and 0.1 mol/l respectively. Introduction of salting out agents (NaCl, CaCl2) and HCl at a constant content of NaClO4 (0.5 mol/l) increases noticeably scandium extraction. For 0.1 mol/l BANT solution in chloroform the extraction capacity in terms of scandium makes up 1.26 g/l. The optimal conditions for the element extraction have been found, the composition of the complex extracted has been ascertained (Sc:BANT:ClO4- = 1:3:3) and extraction mechanism has been suggested. Influence of interfering elements on scandium distribution factor was studied

  13. The relationship between perchlorate in drinking water and cord blood thyroid hormones: First experience from Iran

    Directory of Open Access Journals (Sweden)

    Ashraf Javidi

    2015-01-01

    Full Text Available Background: Considering the controversial information regarding the effects of perchlorate on thyroid function of high risk population as neonates, and given the high prevalence rate of thyroid disorders specially congenital hypothyroidism in our region, this study aims to investigate for the first time in Iran, the relationship between drinking groundwater perchlorate and cord blood thyroid hormones level in an industrial region. Methods: In this cross-sectional study, drinking groundwater perchlorate level of rural areas of Zarinshahr, Isfahan was measured. Simultaneously, cord blood level of thyroid hormones of neonates born in the studied region was measured. Thyroid function test of neonates in regions with low and high perchlorate level were compared. Results: In this study, 25 tap water samples were obtained for perchlorate measurement. Level of cord blood thyroid stimulating hormone (TSH, T4 and T3 of 25 neonates were measured. Mean (standard deviation of perchlorate, TSH, T4 and T3 was 3.59 (5.10 μg/l, 7.81 (4.14 mIU/m, 6.06 (0.85 mg/dl, and 63.46 (17.53 mg/dl, respectively. Mean levels of thyroid function tests were not different in low ( 0.05. Conclusions: Perchlorate did not appear to be related to thyroid function of neonates in the studied industrial region. It seems that iodine status of the regions, as well as other environmental contaminants and genetic background, could impact on its relation with thyroid function of neonates.

  14. A bioassay for the detection of perchlorate in the ppb range.

    Science.gov (United States)

    Heinnickel, Mark; Smith, Stephen C; Koo, Jonathan; O'Connor, Susan M; Coates, John D

    2011-04-01

    A bioassay for the determination of ppb (μg·L(-1)) concentrations of perchlorate has been developed and is described herein. The assay uses the enzyme perchlorate reductase (PR) from the perchlorate-reducing organism Dechloromonas agitata in purified and partially purified forms to detect perchlorate. The redox active dye phenazine methosulfate (PMS) is shown to efficiently shuttle electrons to PR from NADH. Perchlorate can be determined indirectly by monitoring NADH oxidization by PR. To lower the detection limit, we have shown that perchlorate can be concentrated on a solid-phase extraction (SPE) column that is pretreated with the cation decyltrimethylammonium bromide (DTAB). Perchlorate is eluted from these columns with a solution of 2 M NaCl and 200 mM morpholine propane sulfonic acid (MOPS, pH 12.5). By washing these columns with 15 mL of 2.5 mM DTAB and 15% acetone, contaminating ions, such as chlorate and nitrate, are removed without affecting the bioassay. Because of the effect of complex matrices on the SPE columns, the method of standard additions is used to analyze tap water and groundwater samples. The efficacy of the developed bioassay was demonstrated by analyzing samples from 2-17000 ppb in deionized lab water, tap water, and contaminated groundwater. PMID:21384912

  15. Microbial community analysis of perchlorate-reducing cultures growing on zero-valent iron

    International Nuclear Information System (INIS)

    Anaerobic microbial mixed cultures demonstrated its ability to completely remove perchlorate in the presence of zero-valent iron. In order to understand the major microbial reaction in the iron-supported culture, community analysis comprising of microbial fatty acids and polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE) techniques was performed for perchlorate reducing cultures. Analysis of fatty acid methyl esters (FAMEs) and subsequent principal component analysis (PCA) showed clear distinctions not only between iron-supported perchlorate reducing culture and seed bacteria, but also among perchlorate-reducing cultures receiving different electron donors. The DGGE pattern targeting the chlorite dismutase (cld) gene showed that iron-supported perchlorate reducing culture is similar to hydrogen-fed cultures as compared to acetate-fed culture. The phylogenetic tree suggested that the dominant microbial reaction may be a combination of the autotrophic and heterotrophic reduction of perchlorate. Both molecular and chemotaxonomic experimental results support further understanding in the function of zero-valent iron as an adequate electron source for enhancing the microbial perchlorate reduction in natural and engineered systems.

  16. Trivalent chromium sorption on alginate beads

    OpenAIRE

    Araújo, M. Manuela; Teixeira, J.A.

    1997-01-01

    The applicability of trivalent chromium removal from aqueous solutions using calcium alginate beads was studied. The equilibrium isotherms were plotted at two temperatures. The relationship between the chromium sorbed and the calcium released was determined as well as the effect of alginate amount and initial pH on the equilibrium results. Chromium sorption kinetics were evaluated as a function of chromium initial concentration and temperature. Transport properties of trival...

  17. Genetic factors that might lead to different responses in individuals exposed to perchlorate.

    Science.gov (United States)

    Scinicariello, Franco; Murray, H Edward; Smith, Lester; Wilbur, Sharon; Fowler, Bruce A

    2005-11-01

    Perchlorate has been detected in groundwater in many parts of the United States, and recent detection in vegetable and dairy food products indicates that contamination by perchlorate is more widespread than previously thought. Perchlorate is a competitive inhibitor of the sodium iodide symporter, the thyroid cell-surface protein responsible for transporting iodide from the plasma into the thyroid. An estimated 4.3% of the U.S. population is subclinically hypothyroid, and 6.9% of pregnant women may have low iodine intake. Congenital hypothyroidism affects 1 in 3,000 to 1 in 4,000 infants, and 15% of these cases have been attributed to genetic defects. Our objective in this review is to identify genetic biomarkers that would help define subpopulations sensitive to environmental perchlorate exposure. We review the literature to identify genetic defects involved in the iodination process of the thyroid hormone synthesis, particularly defects in iodide transport from circulation into the thyroid cell, defects in iodide transport from the thyroid cell to the follicular lumen (Pendred syndrome), and defects of iodide organification. Furthermore, we summarize relevant studies of perchlorate in humans. Because of perchlorate inhibition of iodide uptake, it is biologically plausible that chronic ingestion of perchlorate through contaminated sources may cause some degree of iodine discharge in populations that are genetically susceptible to defects in the iodination process of the thyroid hormone synthesis, thus deteriorating their conditions. We conclude that future studies linking human disease and environmental perchlorate exposure should consider the genetic makeup of the participants, actual perchlorate exposure levels, and individual iodine intake/excretion levels. PMID:16263499

  18. Perchlorate Exposure Reduces Primordial Germ Cell Number in Female Threespine Stickleback

    Science.gov (United States)

    Petersen, Ann M.; Earp, Nathanial C.; Redmond, Mandy E.; Postlethwait, John H.; von Hippel, Frank A.; Buck, C. Loren; Cresko, William A.

    2016-01-01

    Perchlorate is a common aquatic contaminant that has long been known to affect thyroid function in vertebrates, including humans. More recently perchlorate has been shown to affect primordial sexual differentiation in the aquatic model fishes zebrafish and threespine stickleback, but the mechanism has been unclear. Stickleback exposed to perchlorate from fertilization have increased androgen levels in the embryo and disrupted reproductive morphologies as adults, suggesting that perchlorate could disrupt the earliest stages of primordial sexual differentiation when primordial germ cells (PGCs) begin to form the gonad. Female stickleback have three to four times the number of PGCs as males during the first weeks of development. We hypothesized that perchlorate exposure affects primordial sexual differentiation by reducing the number of germ cells in the gonad during an important window of stickleback sex determination at 14–18 days post fertilization (dpf). We tested this hypothesis by quantifying the number of PGCs at 16 dpf in control and 100 mg/L perchlorate-treated male and female stickleback. Perchlorate exposure from the time of fertilization resulted in significantly reduced PGC number only in genotypic females, suggesting that the masculinizing effects of perchlorate observed in adult stickleback may result from early changes to the number of PGCs at a time critical for sex determination. To our knowledge, this is the first evidence of a connection between an endocrine disruptor and reduction in PGC number prior to the first meiosis during sex determination. These findings suggest that a mode of action of perchlorate on adult reproductive phenotypes in vertebrates, including humans, such as altered fecundity and sex reversal or intersex gonads, may stem from early changes to germ cell development. PMID:27383240

  19. Perchlorate Exposure Reduces Primordial Germ Cell Number in Female Threespine Stickleback.

    Directory of Open Access Journals (Sweden)

    Ann M Petersen

    Full Text Available Perchlorate is a common aquatic contaminant that has long been known to affect thyroid function in vertebrates, including humans. More recently perchlorate has been shown to affect primordial sexual differentiation in the aquatic model fishes zebrafish and threespine stickleback, but the mechanism has been unclear. Stickleback exposed to perchlorate from fertilization have increased androgen levels in the embryo and disrupted reproductive morphologies as adults, suggesting that perchlorate could disrupt the earliest stages of primordial sexual differentiation when primordial germ cells (PGCs begin to form the gonad. Female stickleback have three to four times the number of PGCs as males during the first weeks of development. We hypothesized that perchlorate exposure affects primordial sexual differentiation by reducing the number of germ cells in the gonad during an important window of stickleback sex determination at 14-18 days post fertilization (dpf. We tested this hypothesis by quantifying the number of PGCs at 16 dpf in control and 100 mg/L perchlorate-treated male and female stickleback. Perchlorate exposure from the time of fertilization resulted in significantly reduced PGC number only in genotypic females, suggesting that the masculinizing effects of perchlorate observed in adult stickleback may result from early changes to the number of PGCs at a time critical for sex determination. To our knowledge, this is the first evidence of a connection between an endocrine disruptor and reduction in PGC number prior to the first meiosis during sex determination. These findings suggest that a mode of action of perchlorate on adult reproductive phenotypes in vertebrates, including humans, such as altered fecundity and sex reversal or intersex gonads, may stem from early changes to germ cell development.

  20. On texture formation of chromium electrodeposits

    DEFF Research Database (Denmark)

    Nielsen, Christian Bergenstof; Leisner, Peter; Horsewell, Andy

    1998-01-01

    The microstructure, texture and hardness of electrodeposited hard, direct current (DC) chromium and pulsed reversed chromium has been investigated. These investigations suggest that the growth and texture of hard chromium is controlled by inhibition processes and reactions. Further, it has been...

  1. Chromium Salen Mediated Alkene Epoxidation

    DEFF Research Database (Denmark)

    Petersen, Kaare Brandt; Norrby, Per-Ola; Daly, Adrian M.; Gilheany, Declan G.

    2002-01-01

    The mechanism of alkene epoxidation by chromium(v) oxo salen complexes has been studied by DFT and experimental methods. The reaction is compared to the closely related Mn-catalyzed process in an attempt to understand the dramatic difference in selectivity between the two systems. Overall, the......-spin surface. The low-spin addition of metal oxo species to an alkene leads to an intermediate which forms epoxide either with a barrier on the low-spin surface or without a barrier after spin inversion. Supporting evidence for this intermediate was obtained by using vinylcyclopropane traps. The chromium...

  2. Detoxification of PAX-21 ammunitions wastewater by zero-valent iron for microbial reduction of perchlorate

    Energy Technology Data Exchange (ETDEWEB)

    Ahn, Se Chang; Cha, Daniel K. [Department of Civil and Environmental Engineering, University of Delaware, Newark, DE 19716 (United States); Kim, Byung J. [U.S. Army Engineer Research and Development Center, Champaign, IL 61826-9005 (United States); Oh, Seok-Young, E-mail: quartzoh@ulsan.ac.kr [Department of Civil and Environmental Engineering, University of Ulsan, Ulsan 680-749 (Korea, Republic of)

    2011-08-30

    Highlights: {yields} Ammonium perchlorate, hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) and 2,4-dinitroanisole (DNAN) are the major constituents of PAX-21. {yields} DNAN is identified as the primary toxicant responsible for inhibiting the activity of perchlorate reducing bacteria. {yields} Iron treatment not only removes energetic compounds but also eliminates the toxic constituents that inhibit the subsequent microbial process. - Abstract: US Army and the Department of Defense (DoD) facilities generate perchlorate (ClO{sub 4}{sup -}) from munitions manufacturing and demilitarization processes. Ammonium perchlorate is one of the main constituents in Army's new main charge melt-pour energetic, PAX-21. In addition to ammonium perchlorate, hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) and 2,4-dinitroanisole (DNAN) are the major constituents of PAX-21. In order to evaluate microbial perchlorate reduction as a practical option for the treatment of perchlorate in PAX-21 wastewater, we conducted biodegradation experiments using glucose as the primary sources of electrons and carbon. Batch experiments showed that negligible perchlorate was removed in microbial reactors containing PAX-21 wastewater while control bottles containing seed bacteria and glucose rapidly and completely removed perchlorate. These results suggested that the constituents in PAX-21 wastewater may be toxic to perchlorate reducing bacteria. A series of batch toxicity test was conducted to identify the toxic constituents in PAX-21 and DNAN was identified as the primary toxicant responsible for inhibiting the activity of perchlorate reducing bacteria. It was hypothesized that pretreatment of PAX-21 by zero-valent iron granules will transform toxic constituents in PAX-21 wastewater to non-toxic products. We observed complete reduction of DNAN to 2,4-diaminoanisole (DAAN) and RDX to formaldehyde in abiotic iron reduction study. After a 3-day acclimation period, perchlorate in iron-treated PAX-21

  3. Detoxification of PAX-21 ammunitions wastewater by zero-valent iron for microbial reduction of perchlorate

    International Nuclear Information System (INIS)

    Highlights: → Ammonium perchlorate, hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) and 2,4-dinitroanisole (DNAN) are the major constituents of PAX-21. → DNAN is identified as the primary toxicant responsible for inhibiting the activity of perchlorate reducing bacteria. → Iron treatment not only removes energetic compounds but also eliminates the toxic constituents that inhibit the subsequent microbial process. - Abstract: US Army and the Department of Defense (DoD) facilities generate perchlorate (ClO4-) from munitions manufacturing and demilitarization processes. Ammonium perchlorate is one of the main constituents in Army's new main charge melt-pour energetic, PAX-21. In addition to ammonium perchlorate, hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) and 2,4-dinitroanisole (DNAN) are the major constituents of PAX-21. In order to evaluate microbial perchlorate reduction as a practical option for the treatment of perchlorate in PAX-21 wastewater, we conducted biodegradation experiments using glucose as the primary sources of electrons and carbon. Batch experiments showed that negligible perchlorate was removed in microbial reactors containing PAX-21 wastewater while control bottles containing seed bacteria and glucose rapidly and completely removed perchlorate. These results suggested that the constituents in PAX-21 wastewater may be toxic to perchlorate reducing bacteria. A series of batch toxicity test was conducted to identify the toxic constituents in PAX-21 and DNAN was identified as the primary toxicant responsible for inhibiting the activity of perchlorate reducing bacteria. It was hypothesized that pretreatment of PAX-21 by zero-valent iron granules will transform toxic constituents in PAX-21 wastewater to non-toxic products. We observed complete reduction of DNAN to 2,4-diaminoanisole (DAAN) and RDX to formaldehyde in abiotic iron reduction study. After a 3-day acclimation period, perchlorate in iron-treated PAX-21 wastewater was rapidly decreased to

  4. Chromium content of selected Greek foods.

    Science.gov (United States)

    Bratakos, Michael S; Lazos, Evangelos S; Bratakos, Sotirios M

    2002-05-01

    The total chromium content of a wide variety of Greek foods was determined by graphite furnace atomic absorption spectroscopy (GFAAS). Meat, fish and seafood, cereals and pulses were rich sources of chromium (>0.100 microg/g). Fruits, milk, oils and fats and sugar were poor sources. Differences in chromium content were found between different food classes from Greece and those from some other countries. Based on available food consumption data and chromium levels in this study, it was estimated that the chromium intake of Greeks is 143 microg/day, with vegetables, cereals and meat being the main contributors. PMID:12083715

  5. Effect of nitrate, acetate, and hydrogen on native perchlorate-reducing microbial communities and their activity in vadose soil.

    Science.gov (United States)

    Nozawa-Inoue, Mamie; Jien, Mercy; Yang, Kun; Rolston, Dennis E; Hristova, Krassimira R; Scow, Kate M

    2011-05-01

    The effect of nitrate, acetate, and hydrogen on native perchlorate-reducing bacteria (PRB) was examined by conducting microcosm tests using vadose soil collected from a perchlorate-contaminated site. The rate of perchlorate reduction was enhanced by hydrogen amendment and inhibited by acetate amendment, compared with unamendment. Nitrate was reduced before perchlorate in all amendments. In hydrogen-amended and unamended soils, nitrate delayed perchlorate reduction, suggesting that the PRB preferentially use nitrate as an electron acceptor. In contrast, nitrate eliminated the inhibitory effect of acetate amendment on perchlorate reduction and increased the rate and the extent, possibly because the preceding nitrate reduction/denitrification decreased the acetate concentration that was inhibitory to the native PRB. In hydrogen-amended and unamended soils, perchlorate reductase gene (pcrA) copies, representing PRB densities, increased with either perchlorate or nitrate reduction, suggesting that either perchlorate or nitrate stimulates the growth of the PRB. In contrast, in acetate-amended soil pcrA increased only when perchlorate was depleted: a large portion of the PRB may have not utilized nitrate in this amendment. Nitrate addition did not alter the distribution of the dominant pcrA clones in hydrogen-amended soil, likely because of the functional redundancy of PRB as nitrate-reducers/denitrifiers, whereas acetate selected different pcrA clones from those with hydrogen amendment. PMID:21284679

  6. Determination of chromium combined with DNA, RNA and protein in chromium-rich brewer's yeast

    International Nuclear Information System (INIS)

    The contents of chromium in the DNA, RNA and protein fractions separated from chromium-rich and normal brewer's yeast were determined with the neutron activation analysis in order to study the combination of Cr with DNA, RNA and protein in chromium-rich brewer's yeast. The results showed that the extracting rats and concentrations of DNA, RNA and protein had no significant difference in two types of yeast, but the chromium contents of DNA, RNA and protein in the chromium-rich yeast were significantly higher than those in the normal. In addition, the content of chromium in DNA was much higher than that in RNA and protein, which indicated that the inorganic chromium compounds entered into the yeast cell, during the yeast cultivation in the culture medium containing chromium were converted into organic chromium compounds combined with DNA, RNA and protein

  7. A rapid and simple method for the separation of TBP-dodecane by perchloric acid

    International Nuclear Information System (INIS)

    Organic solvents, including TBP etc., are widely used as an extractant, and treated and disposed by storage, incineration, and absorption into absorbent after they were used. Any of those methods does not aim at recycling of solvents, treating concurrently the extractant and the diluent without separating them. In this paper, a test is reported on the TBP-dodecane separation by perchloric acid for a separation test of the diluent from the extractant as a first step toward recycling. Basically this separation method is already reported by P. Mark et al. as a method for the analysis of TBP, but it requires a large amount of perchloric acid. With a further detailed study of the perchloric acid effects on the TBP-dodecane separation, it was made clear that the separation is possible by adding a fixed amount of TBP contacted with perchloric acid to the TBP-dodecane solvent. In this paper, its outline is presented. (author)

  8. ANALYSIS OF HYDROPONIC FERTILIZER MATRIXES FOR PERCHLORATE: COMPARISON OF ANALYTICAL TECHNIQUES

    Science.gov (United States)

    Seven retail hydroponic nitrate fertilizer products, two liquid and five solid, were comparatively analyzed for the perchlorate anion (ClO4-) by ion chromatography (IC) with suppressed conductivity detection, complexation electrospray ionization mass spectrometry (cESI-MS), norma...

  9. Radioiodine tracers as useful tools in studies of thyrotoxic effects of exogenous bromide and perchlorate ions

    International Nuclear Information System (INIS)

    With the use of 125I and 131I radionuclides, we followed the effects of exogenous bromide and perchlorate ions on the metabolism of iodine and of thyroid hormone in the rat. The presumed thyrotoxic effects of bromide and perchlorate have been confirmed and quantified. Correct assay conditions for the radiometric determination of the enzyme activity of thyroid peroxidase (TPO) have been established. The use of the adapted radiometric assay revealed a divergent influence of bromide and perchlorate ions on the TPO activity in the rat thyroids. Excessive bromide exerted a biphasic effect, depending on the extent of bromide intake in the animals. In contrast, in all the rats that were administered with high amounts of perchlorate were found elevated TPO activities. (author)

  10. On the stability of perchlorate ions against reductive attacks in electrochemical systems and in the environment

    Directory of Open Access Journals (Sweden)

    GYŐZŐ G. LÁNG

    2011-08-01

    Full Text Available The problems related to the electrochemical/electrocatalytic stability of perchlorate ions are reviewed in the light of recent experimental results. The electrocatalytic, catalytic, and electrochemical reduction processes are presented and the links between them are outlined. Some possible mechanisms of the complicated reduction processes are discussed. Various methods for the detection of reduction process are presented, e.g. voltammetry, impedance spectroscopy, and radiotracer methods. Environmental aspects and some methods for perchlorate removal and wastewater treatment are briefly summarized.

  11. The perchlorate discharge test with 123I for the diagnosis of the Pendred syndrome in children

    International Nuclear Information System (INIS)

    The method for the diagnosis of the Pendred Syndrome in children by the Perchlorate discharge test using 123I is described. The older child, who has the Pendred Syndrome and the obligatory hearing deficit, frequently has neither a goitre nor hypothyroidism, but other investigations (bone growth, scars and function tests) can also show changes. However a more certain diagnosis of this disorder in children is possible by the perchlorate discharge test using 123I. (orig.)

  12. Behavioral response of dissimilatory perchlorate-reducing bacteria to different electron acceptors

    OpenAIRE

    Sun, Yvonne; Gustavson, Ruth L.; Ali, Nadia; Weber, Karrie A.; Westphal, Lacey L.; Coates, John D.

    2009-01-01

    The response behavior of three dissimilatory perchlorate-reducing bacteria to different electron acceptors (nitrate, chlorate, and perchlorate) was investigated with two different assays. The observed response was species-specific, dependent on the prior growth conditions, and was inhibited by oxygen. We observed attraction toward nitrate when Dechloromonas aromatica strain RCB and Azospira suillum strain PS were grown with nitrate. When D. aromatica and Dechloromonas agitata strain CKB were ...

  13. Perchlorate in dust fall and indoor dust in Malta: An effect of fireworks.

    Science.gov (United States)

    Vella, Alfred J; Chircop, Cynthia; Micallef, Tamara; Pace, Colette

    2015-07-15

    We report on the presence of perchlorate in the settleable dust of Malta, a small central Mediterranean island. Both dust fall collected directly as it precipitated from atmosphere over a period of one month and deposited indoor dust from domestic residences were studied. Perchlorate was determined by ion chromatography of water extracts of the collected dusts. Dust fall was collected from 43 towns during 2011 to 2013 and indoor dust was sampled from homes in the same localities. Perchlorate was detected in 108 of 153 samples of dust fall (71%) and in 28 of 37 indoor dust samples (76%). Detectable perchlorate in dust fall ranged from 0.52μgg(-1) to 561μgg(-1) with a median value of 6.2μgg(-1); in indoor dust, levels were from 0.79μgg(-1) to 53μgg(-1) with a median value of 7.8μgg(-1), the highest recorded anywhere to date. Statistical analysis suggested that there was no significant difference in perchlorate content of indoor dust and dust fall. Perchlorate levels in dust fall escalate during the summer in response to numerous religious feasts celebrated with fireworks and perchlorate persists at low μgg(-1) concentrations for several months beyond the summer festive period. In Malta, perchlorate derives exclusively from KClO4, imported for fireworks manufacture. Its residue in dust presents an exposure risk to the population, especially via ingestion by hand to mouth transfer. Our results suggest that wherever intensive burning of fireworks takes place, the environmental impact may be much longer lived than realised, mainly due to re-suspension and deposition of contaminated settled dust in the urban environment. PMID:25828411

  14. Microbial redox processes in deep subsurface environments and the potential application of (perchlorate in oil reservoirs

    Directory of Open Access Journals (Sweden)

    Martin G Liebensteiner

    2014-09-01

    Full Text Available The ability of microorganisms to thrive under oxygen-free conditions in subsurface environments relies on the enzymatic reduction of oxidized elements, such as sulfate, ferric iron or CO2, coupled to the oxidation of inorganic or organic compounds. A broad phylogenetic and functional diversity of microorganisms from subsurface environments has been described using isolation-based and advanced molecular ecological techniques. The physiological groups reviewed here comprise iron-, manganese- and nitrate-reducing microorganisms. In the context of recent findings also the potential of chlorate and perchlorate [jointly termed (perchlorate] reduction in oil reservoirs will be discussed. Special attention is given to elevated temperatures that are predominant in the deep subsurface. Microbial reduction of (perchlorate is a thermodynamically favorable redox process, also at high temperature. However, knowledge about (perchlorate reduction at elevated temperatures is still scarce and restricted to members of the Firmicutes and the archaeon Archaeoglobus fulgidus. By analyzing the diversity and phylogenetic distribution of functional genes in (metagenome databases and combining this knowledge with extrapolations to earlier-made physiological observations we speculate on the potential of (perchlorate reduction in the subsurface and more precisely oil fields. In addition, the application of (perchlorate for bioremediation, souring control and microbial enhanced oil recovery are addressed.

  15. Preliminary analyses for perchlorate in selected natural materials and their derivative products

    Science.gov (United States)

    Orris, G.J.; Harvey, G.J.; Tsui, D.T.; Eldrige, J.E.

    2003-01-01

    Increasing concern about sources of perchlorate contamination in ground and surface waters has led to interest in identifying potential sources of natural perchlorate and products derived from these natural sources. To date, most perchlorate found in ground and surface waters has been attributed to its major uses as an oxidizer in solid propellants for rockets, in fireworks and other explosives, and a variety of other uses of man-made perchlorate salts. However, perchlorate found in the soils, surface water, and ground water of some locations cannot be linked to an anthropogenic source. This paper contains preliminary data on the detection and non-detection of perchlorate in a variety of natural materials and their products, including some fertilizer materials. These data were previously presented at two conferences; once in poster session and once orally (Harvey and others, 1999; Orris and others, 2000). Although the results presented here are included in a journal article awaiting publication, the lack of public information on this topic has led to repeated requests for the data used as the basis for our presentations in 1999 and 2000.

  16. A screened hybrid density functional study on energetic complexes: Cobalt, nickel and copper carbohydrazide perchlorates

    International Nuclear Information System (INIS)

    Graphical abstract: The molecular geometry, electronic structure, infrared spectra, and heats of reaction and formation of cobalt and nickel tris(carbohydrazide) perchlorates as well as copper bis(carbohydrazide) perchlorate are investigated using the HSE screened hybrid density functional. The metal-ligand interaction, thermal stability, and red-shift of the amino stretching vibrations of these complexes are also discussed. Moreover, it is found there is a relationship between the energy gap and impact sensitivity. - Abstract: The molecular geometry, electronic structure, infrared spectra and thermochemical properties of cobalt and nickel tris(carbohydrazide) perchlorates (CoCP and NiCP) as well as copper bis(carbohydrazide) perchlorate (CuCP) were investigated using the Heyd-Scuseria-Ernzerhof (HSE) screened hybrid density functional. The results show that both perchlorate ions coordinate with the copper atom, and the interactions between copper and perchlorate are ionic, whereas all the metal-carbohydrazide interactions are covalent. Due to the delocalization from the σN-H bond orbital to the n*M antibond orbital, the amino stretching vibrations of these complexes show considerable red-shift compared with those of free carbohydrazide ligand. The calculated heats of reaction and formation indicate that the formations of these complexes are exothermic, and the order of their thermal stability is NiCP > CoCP > CuCP. These agree well with the experimental results. Finally, we find that there is a relationship between the energy gap and impact sensitivity.

  17. Mechanistic Studies on the Radiolytic Decomposition of Perchlorates on the Martian Surface

    Science.gov (United States)

    Turner, Andrew M.; Abplanalp, Matthew J.; Kaiser, Ralf I.

    2016-04-01

    Perchlorates—inorganic compounds carrying the perchlorate ion ({{ClO}}4{}-)—were discovered at the north polar landing site of the Phoenix spacecraft and at the southern equatorial landing site of the Curiosity Rover within the Martian soil at levels of 0.4-0.6 wt%. This study explores in laboratory experiments the temperature-dependent decomposition mechanisms of hydrated perchlorates—namely magnesium perchlorate hexahydrate (Mg(ClO4)2·6H2O)—and provides yields of the oxygen-bearing species formed in these processes at Mars-relevant surface temperatures from 165 to 310 K in the presence of galactic cosmic-ray particles (GCRs). Our experiments reveal that the response of the perchlorates to the energetic electrons is dictated by the destruction of the perchlorate ion ({{ClO}}4{}-) and the inherent formation of chlorates ({{ClO}}3{}-) plus atomic oxygen (O). Isotopic substitution experiments reveal that the oxygen is released solely from the perchlorate ion and not from the water of hydration (H2O). As the mass spectrometer detects only molecular oxygen (O2) and no atomic oxygen (O), atomic oxygen recombines to molecular oxygen within the perchlorates, with the overall yield of molecular oxygen increasing as the temperature drops from 260 to 160 K. Absolute destruction rates and formation yields of oxygen are provided for the planetary modeling community.

  18. High-nitrogen-based pyrotechnics: perchlorate-free red- and green-light illuminants based on 5-aminotetrazole.

    Science.gov (United States)

    Sabatini, Jesse J; Moretti, Jared D

    2013-09-16

    Prototype testing of perchlorate-free hand-held signal illuminants for the US Army's M126 A1 red-star and M195 green-star parachute illuminants are described. Although previous perchlorate-free variants for these items have been developed based on high-nitrogen compounds that are not readily available, the new formulations consist of anhydrous 5-aminotetrazole as the suitable perchlorate replacement. Compared to the perchlorate-containing control, the disclosed illuminants exhibited excellent stabilities toward various ignition stimuli and had excellent pyrotechnic performance. The illuminants are important from both military and civil fireworks perspectives, as the perchlorate-free nature of the illuminants adequately address environmental concerns associated with perchlorate-containing red- and green-light-emitting illuminants. PMID:23950104

  19. Tissues and urinary chromium concentrations in rats fed high-chromium diets

    International Nuclear Information System (INIS)

    Complete text of publication follows. Chromium is an essential trace elements and enhances the function of insulin as a form of chromodulin. In the subjects with a certain type of diabetics, 200 to 1,000 μg/d of chromium is administered to reduced the symptoms of diabetics. However, although there are not any health-promotive effects of chromium-administration in healthy subjects, various types of chromium supplements are commercially available in many countries; the adverse effects caused by an excessive chromium intake are feared. In the present study, to clarify the tolerable upper limit of chromium, tissue and urinary chromium concentrations, liver function and iron status were examined in rats fed high-chromium diets. Thirty-six male 4-weeks Wistar rats were divided into six groups and fed casein-based diets containing 1, 10 or 100 μg/g of chromium as chromium chloride (CrCl3) or chromium picolinate (CrPic) for 4 weeks. After the feeding, chromium concentrations in liver, kidney, small intestine and tibia were determined by inductively coupled plasma-mass spectrometry. In addition, urine samples were collected on 3rd to 4th week and their chromium concentrations were also determined. Chromium concentrations in liver, kidney, small intestine and tibia were elevated with increase of dietary chromium concentration. Urinary chromium excretion was also elevated with the increase of dietary chromium and the rate of urinary chromium excretion was less than 2% to dietary chromium intake in all the experimental groups. In the administration of 100 μg/g of chromium, rats given CrCl3 showed significantly higher tibia chromium concentration and lower urinary chromium excretion than those given CrPic. There were not any differences in iron status among the experimental groups. Activities of serum aspartate aminotransferase and alanine aminotransferase in rats fed diet containing 100 μg/g of chromium as CrPic were significantly higher than those in rats fed other diets.

  20. Inhibition of microbial sulfate reduction in a flow-through column system by (per)chlorate treatment

    OpenAIRE

    Anna eEngelbrektson; Christopher eHubbard; Lauren eTom; Aaron eBOUSSINA; Yong Tae eJin; Hayden eWong; Yvette Marisa Piceno; Hans Karl Carlson; Mark eConrad; Andersen, Gary L.; Coates, John D.

    2014-01-01

    Microbial sulfate reduction is a primary cause of oil reservoir souring. Here we show that amendment with chlorate or perchlorate [collectively (per)chlorate] potentially resolves this issue. Triplicate packed columns inoculated with marine sediment were flushed with coastal water amended with yeast extract and one of nitrate, chlorate, or perchlorate. Results showed that although sulfide production was dramatically reduced by all treatments, effluent sulfide was observed in the nitrate (10 m...

  1. High-performing red-light-emitting pyrotechnic illuminants through the use of perchlorate-free materials.

    Science.gov (United States)

    Moretti, Jared D; Sabatini, Jesse J; Poret, Jay C

    2014-07-01

    The development of perchlorate-free M662 40 mm illuminating pyrotechnic compositions is described. On the bases of cost, performance, and sensitivity, potassium periodate was determined to be most effective potassium perchlorate replacement in the compositions tested. The optimal periodate-based composition exceeded the performance of the perchlorate-containing control, exhibited low sensitivity values to impact, friction, and electrostatic discharge, and had high thermal onset temperatures. PMID:24939042

  2. Perchlorate in the San Antonio Segment of the Edwards Aquifer, Texas

    Science.gov (United States)

    Fahlquist, L.; Rajagapolan, S.; Jackson, W. A.

    2007-12-01

    Perchlorate has been detected in drinking-water supplies and can have adverse health effects on humans by disrupting thyroid function. Perchlorate and other constituents were analyzed from ground-water samples that were collected in 2004-06 from 99 wells completed in the San Antonio segment of the Edwards aquifer as part of the U.S. Geological Survey National Water-Quality Assessment Program. The fractured karstic carbonate Edwards aquifer, declared a sole-source aquifer by the U.S. Environmental Protection Agency, supplies nearly one-half million acre-feet per year for drinking water and other uses. Wells were located in a variety of land-use settings that included rangeland, agriculture, and urban; well types included domestic, public, and observation. Perchlorate was detected in 98 percent of the samples, and concentrations ranged from less than 0.05 to 3 micrograms per liter (μg/L). Five samples contained concentrations greater than 1 μg/L and were from wells in the urban northern San Antonio area. The results from three samples that contained perchlorate at concentrations greater than 2 μg/L are anomalous. Chloride concentration ranged from 5.6 to 69 milligrams per liter, typical for freshwater in the Edwards aquifer. No significant (r2 greater than 0.7) correlations were observed when perchlorate concentrations were correlated with depth to water, total depth of well, or concentrations of bicarbonate, nitrate, phosphate, sulfate, bromide, chloride, fluoride, calcium, magnesium, potassium, sodium, strontium, and dissolved solids. Tritium concentrations ranged from 1.2 to 2.9 tritium units in 31 of the 99 samples and indicate at least some fraction of modern water (post-atmospheric nuclear tests). No correlation between apparent tritium age and perchlorate concentration was observed, a possible indication that anthropogenic influences are not affecting observed perchlorate concentrations. The molar ratio of chloride to perchlorate ranged from 17,000 to 320

  3. Study of microbial perchlorate reduction: Considering of multiple pH, electron acceptors and donors

    Energy Technology Data Exchange (ETDEWEB)

    Xu, Xing [Key Laboratory of Water Pollution Control and Recycling (Shandong), School of Environmental Science and Engineering, Shandong University, Jinan 250100 (China); Gao, Baoyu, E-mail: bygao@sdu.edu.cn [Key Laboratory of Water Pollution Control and Recycling (Shandong), School of Environmental Science and Engineering, Shandong University, Jinan 250100 (China); Jin, Bo [School of Chemical Engineering, The University of Adelaide, Adelaide SA 5005,Australia (Australia); Zhen, Hu [Key Laboratory of Water Pollution Control and Recycling (Shandong), School of Environmental Science and Engineering, Shandong University, Jinan 250100 (China); Wang, Xiaoyi [CSIRO Land and Water, Gate 5, Waite Road, Urrbrae, SA 5064 (Australia); Dai, Ming [School of Chemical Engineering, The University of Adelaide, Adelaide SA 5005,Australia (Australia)

    2015-03-21

    Graphical abstract: Schemes of perchlorate reduction in ClO{sub 4}{sup −}/ClO{sub 3}{sup −}–NO{sub 3}{sup −} e{sup −}acceptor systems. - Highlights: • We created a multiple electron acceptor/donor system for ClO{sub 4}{sup −} reduction. • Nitrate reduction was inhibited when using perchlorate-grown Azospira sp. KJ. • Reduction proceeded as an order of ClO{sub 3}{sup −}, ClO{sub 4}{sup −}and NO{sub 3}{sup −}. • Oxidation of acetate was inhibited by succinate in acetate–succinate series. - Abstract: Bioremediation of perchlorate-cotaminated water by a heterotrophic perchlorate reducing bacterium creates a multiple electron acceptor-donor system. We experimentally determined the perchlorate reduction by Azospira sp. KJ at multiple pH, electron acceptors and donors systems; this was the aim of this study. Perchlorate reduction was drastically inhibited at the pH 6.0, and the maximum reduction of perchlorate by Azospira sp. KJ was observed at pH value of 8.0. Perchlorate reduction was retarded in ClO{sub 4}{sup −}–ClO{sub 3}{sup −}, ClO{sub 4}{sup −}–ClO{sub 3}{sup −}–NO{sub 3}{sup −},and ClO{sub 4}{sup −}–NO{sub 3}{sup −} acceptor systems, while being completely inhibited by the additional O{sub 2} in the ClO{sub 4}{sup −}–O{sub 2} acceptor system. The reduction proceeded as an order of ClO{sub 3}{sup −}, ClO{sub 4}{sup −}, and NO{sub 3}{sup −} in the ClO{sub 4}{sup −}–ClO{sub 3}{sup −}–NO{sub 3}{sup −} system. K{sub S,}v{sub max}, and q{sub max} obtained at different e{sup −} acceptor and donor conditions are calculated as 140.5–190.6 mg/L, 8.7–13.2 mg-perchlorate/L-h, and 0.094–0.16 mg-perchlorate/mg-DW-h, respectively.

  4. Study of microbial perchlorate reduction: Considering of multiple pH, electron acceptors and donors

    International Nuclear Information System (INIS)

    Graphical abstract: Schemes of perchlorate reduction in ClO4−/ClO3−–NO3− e−acceptor systems. - Highlights: • We created a multiple electron acceptor/donor system for ClO4− reduction. • Nitrate reduction was inhibited when using perchlorate-grown Azospira sp. KJ. • Reduction proceeded as an order of ClO3−, ClO4−and NO3−. • Oxidation of acetate was inhibited by succinate in acetate–succinate series. - Abstract: Bioremediation of perchlorate-cotaminated water by a heterotrophic perchlorate reducing bacterium creates a multiple electron acceptor-donor system. We experimentally determined the perchlorate reduction by Azospira sp. KJ at multiple pH, electron acceptors and donors systems; this was the aim of this study. Perchlorate reduction was drastically inhibited at the pH 6.0, and the maximum reduction of perchlorate by Azospira sp. KJ was observed at pH value of 8.0. Perchlorate reduction was retarded in ClO4−–ClO3−, ClO4−–ClO3−–NO3−,and ClO4−–NO3− acceptor systems, while being completely inhibited by the additional O2 in the ClO4−–O2 acceptor system. The reduction proceeded as an order of ClO3−, ClO4−, and NO3− in the ClO4−–ClO3−–NO3− system. KS,vmax, and qmax obtained at different e− acceptor and donor conditions are calculated as 140.5–190.6 mg/L, 8.7–13.2 mg-perchlorate/L-h, and 0.094–0.16 mg-perchlorate/mg-DW-h, respectively

  5. Particle size distribution and perchlorate levels in settled dust from urban roads, parks, and roofs in Chengdu, China.

    Science.gov (United States)

    Li, Yiwen; Shen, Yang; Pi, Lu; Hu, Wenli; Chen, Mengqin; Luo, Yan; Li, Zhi; Su, Shijun; Ding, Sanglan; Gan, Zhiwei

    2016-01-01

    A total of 27 settled dust samples were collected from urban roads, parks, and roofs in Chengdu, China to investigate particle size distribution and perchlorate levels in different size fractions. Briefly, fine particle size fractions (intake is safe to both children and adults in Chengdu, China. However, due to perchlorate mainly existing in fine particles, there is a potential for perchlorate to transfer into surface water and the atmosphere by runoff and wind erosion or traffic emission, and this could act as an important perchlorate pollution source for the indoor environment, and merits further study. PMID:26608047

  6. Americium(3) solvent extraction by oxides of dialkyl(diaryl)[dialkylcarbamoylmethyl]phosphines (CMPO) from perchloric acid solutions

    International Nuclear Information System (INIS)

    Extraction of americium(3) from perchloric acid solutions by CMPO was investigated. It is shown that americium(3) is much more effectively extracted from perchloric acid solutions, than from nitric acid ones, and increase in americium distribution coefficient depends considerably on reagent nature. As a consequence, anomalous aryl effect increases significantly in perchloric acid solutions. The value of anomalous aryl effect depends directly on stoichiometry of extracted complexes in nitric acid and perchloric acid media. Conditions for extractional concentration of americium up to the 100-fold one with small reagent consumption were suggested

  7. Food Chromium Contents, Chromium Dietary Intakes And Related Biological Variables In French Free-Living Elderly

    Science.gov (United States)

    Chromium (Cr III), an essential trace element, functions in potentiating insulin sensitivity, regulating glucose homeostasis, improving lipid profile, and maintaining lean body mass. Glucose intolerance and chromium deficiency increase with age, and could be aggravating factors of the metabolic synd...

  8. Soils contaminated with hexavalent chromium

    OpenAIRE

    Fonseca, Bruna Catarina da Silva

    2011-01-01

    Tese de doutoramento em Engenharia Química e Biológica The interest in environmental soil science has been growing in the last years due to the continuous degradation of this major natural resource. With this in mind, and because chromium and lead are two of the most toxic heavy metals frequently detected as soil contaminants in the Portuguese territory, the study and development of few remediation techniques and the indissociable description of the sorption and migration of...

  9. Carbon, chromium and molybdenum contents

    International Nuclear Information System (INIS)

    This work describes solidification experiments on white cast iron, with 15 and 20% of chromium, 2.3, 3.0 and 3.6 % of carbon and 0.0, 1.5 and 2.5 % of molybdenum in test de samples with 30 mm diameter. Measurements were performed on the austenite and eutectic formation arrests, the number of the eutectic carbide particles relative to the total and the eutectic volumes, and the volume fraction of the primary austenite

  10. Soil Flushing Through a Thick Vadose Zone: Perchlorate Removal Documented at Edwards AFB, California

    Science.gov (United States)

    Battey, T. F.; Shepard, A. J.; Tait, R. J.

    2007-12-01

    There are currently few viable alternatives for perchlorate remediation in the vadose zone, particularly for the relatively thick vadose zones that are typical in the arid southwest where many perchlorate sites occur. Perchlorate in the vadose zone occurs in the form of highly soluble salts that may represent a risk to human or ecological receptors, and may also represent a threat to the underlying groundwater. A soil flushing treatability study was conducted at Edwards Air Force Base in the Mojave Desert of southern California at a site with a 129-foot thick vadose zone consisting primarily of clayey sand. This study utilized an infiltration gallery in conjunction with extraction, treatment, and re-injection of groundwater at the site, which contained perchlorate-contaminated soil and groundwater. The study objective was to evaluate the effectiveness of the infiltration gallery to 1) introduce treated groundwater back into the aquifer and 2) wash the perchlorate from the vadose zone soils to the aquifer. The infiltration gallery consisted of slotted PVC pipes within a highly permeable engineered bed of washed gravel. The initial water introduced into the gallery was amended with potassium bromide tracer. A downhole neutron probe was used to track the movement of the wetting front downward and outward from the gallery. Successive neutron measurements in vertical access tubes revealed that the introduced water reached the 125-foot bottom of the access tubes 14 weeks after the water was introduced into the gallery. The bromide tracer was detected in groundwater immediately below the gallery approximately 1 week later. The infiltration gallery was able to sustain an average flow rate of 2.3 gallons per minute. Prior to infiltration, the perchlorate concentration in groundwater below the gallery was 4,500 µg/L. Approximately 18 weeks after the start of infiltration, a perchlorate spike of 72,400 µg/L was detected below the gallery. The increase in perchlorate

  11. Preparation and Characterization of Nanocrystalline Hard Chromium Coatings Using Eco-Friendly Trivalent Chromium Bath

    OpenAIRE

    V. S. Protsenko; V. O Gordiienko; Danilov, F. I.; Kwon, S.C.

    2011-01-01

    A new aqueous sulfate trivalent chromium bath is described. The chromium bath contains formic acid and carbamide as complexing agents. Chromium was deposited at a temperature of 30÷40 oC and a cathode current density of 10÷25 A dm-2. The bath allows obtaining thick (up to several hundred micrometers) hard chromium coatings with nanocrystalline structure. The electrodeposition rate reaches 0.8÷0.9 µm min-1.

  12. REMOVAL OF HEXAVALENT CHROMIUM FROM DRINKING WATER

    OpenAIRE

    A. R. Asgari ، F. Vaezi ، S. Nasseri ، O. Dördelmann ، A. H. Mahvi ، E. Dehghani Fard

    2008-01-01

    Removal of chromium can be accomplished by various methods but none of them is cost-effective in meeting drinking water standards. For this study, granular ferric hydroxide was used as adsorbent for removal of hexavalent chromium. Besides, the effects of changing contact time, pH and concentrations of competitive anions were determined for different amounts of granular ferric hydroxide. It was found that granular ferric hydroxide has a high capacity for adsorption of hexavalent chromium from ...

  13. Inoculation of chromium white cast iron

    Directory of Open Access Journals (Sweden)

    D. Kopyciński

    2009-01-01

    Full Text Available It has been proved that an addition of boron carbide introduced as an inoculant to the chromium white cast iron changes the structureof castings. Castings after inoculation revealed a different structure with numerous grains. Primary precipitates of chromium carbide also appeared, reducing the mechanical properties of as-cast parts. Properly established heat treatment regime makes chromium iron castings regain their, originally high, mechanical properties.

  14. Inoculation of chromium white cast iron

    OpenAIRE

    D. Kopyciński

    2009-01-01

    It has been proved that an addition of boron carbide introduced as an inoculant to the chromium white cast iron changes the structureof castings. Castings after inoculation revealed a different structure with numerous grains. Primary precipitates of chromium carbide also appeared, reducing the mechanical properties of as-cast parts. Properly established heat treatment regime makes chromium iron castings regain their, originally high, mechanical properties.

  15. Inhibition of microbial sulfate reduction in a flow-through column system by (perchlorate treatment

    Directory of Open Access Journals (Sweden)

    Anna eEngelbrektson

    2014-06-01

    Full Text Available Microbial sulfate reduction is a primary cause of oil reservoir souring. Here we show that amendment with chlorate or perchlorate [collectively (perchlorate] potentially resolves this issue. Triplicate packed columns inoculated with marine sediment were flushed with coastal water amended with yeast extract and one of nitrate, chlorate, or perchlorate. Results showed that although sulfide production was dramatically reduced by all treatments, effluent sulfide was observed in the nitrate (10 mM treatment after an initial inhibition period. In contrast, no effluent sulfide was observed with (perchlorate (10 mM. Microbial community analyses indicated temporal community shifts and phylogenetic clustering by treatment. Nitrate addition stimulated Xanthomonadaceae and Rhizobiaceae growth, supporting their role in nitrate metabolism. (Perchlorate showed distinct effects on microbial community structure compared with nitrate and resulted in a general suppression of the community relative to the untreated control combined with a significant decrease in sulfate reducing species abundance indicating specific toxicity. Furthermore, chlorate stimulated Pseudomonadaceae and Pseudoalteromonadaceae, members of which are known chlorate respirers, suggesting that chlorate may also control sulfidogenesis by biocompetitive exclusion of sulfate-reduction. Perchlorate addition stimulated Desulfobulbaceae and Desulfomonadaceae, which contain sulfide oxidizing and elemental sulfur-reducing species respectively, suggesting that effluent sulfide concentrations may be controlled through sulfur redox cycling in addition to toxicity and biocompetitive exclusion. Sulfur isotope analyses further support sulfur cycling in the columns, even when sulfide is not detected. This study indicates that (perchlorate show great promise as inhibitors of sulfidogenesis in natural communities and provides insight into which organisms and respiratory processes are involved.

  16. Structure, phase transitions and molecular motions in 4-aminopyridinium perchlorate

    Science.gov (United States)

    Czupinski, O.; Bator, G.; Ciunik, Z.; Jakubas, R.; Medycki, W.; Swiergiel, J.

    2002-09-01

    The crystal structure of the 4-aminopyridinium perchlorate (4-apyH)ClO4 has been determined at 100 K by means of x-ray diffraction as monoclinic, with space group P 21, with Z = 8. The crystal undergoes two structural phase transitions: one of first-order type, reversible, at 241/243 K (on cooling/heating respectively) and one of weakly first-order type, irreversible, at 277 K (on heating). The crystal dynamics is discussed on the basis of the temperature dependence of the 1 H nuclear magnetic resonance second moment (M2) and spin-lattice relaxation time T1. Both phase transitions are interpreted in terms of the changes in the motional state of (4-apyH)+ cations and ClO4- anions. The dielectric dispersion studies disclose a relaxation process over the high-temperature phase (above 241 K) in the audio-frequency region. The dielectric results are described by a Cole-Cole equation. The title crystal reveals pyroelectric properties below 241 K. The ferroelastic domain structure of (4-apyH)ClO4 is observed over the whole temperature range studied.

  17. Structure, phase transitions and molecular motions in 4-aminopyridinium perchlorate

    International Nuclear Information System (INIS)

    The crystal structure of the 4-aminopyridinium perchlorate (4-apyH)ClO4 has been determined at 100 K by means of x-ray diffraction as monoclinic, with space group P 21, with Z=8. The crystal undergoes two structural phase transitions: one of first-order type, reversible, at 241/243 K (on cooling/heating respectively) and one of weakly first-order type, irreversible, at 277 K (on heating). The crystal dynamics is discussed on the basis of the temperature dependence of the 1H nuclear magnetic resonance second moment (M2) and spin-lattice relaxation time T1. Both phase transitions are interpreted in terms of the changes in the motional state of (4-apyH)+ cations and ClO4- anions. The dielectric dispersion studies disclose a relaxation process over the high-temperature phase (above 241 K) in the audio-frequency region. The dielectric results are described by a Cole-Cole equation. The title crystal reveals pyroelectric properties below 241 K. The ferroelastic domain structure of (4-apyH)ClO4 is observed over the whole temperature range studied. (author)

  18. Structure, phase transitions and molecular motions in 4-aminopyridinium perchlorate

    Energy Technology Data Exchange (ETDEWEB)

    Czupinski, O.; Bator, G.; Ciunik, Z.; Jakubas, R. [Faculty of Chemistry, University of Wroclaw, Wroclaw (Poland); Medycki, W.; Swiergiel, J. [Institute of Molecular Physics, PAS, Poznan (Poland)

    2002-09-16

    The crystal structure of the 4-aminopyridinium perchlorate (4-apyH)ClO{sub 4} has been determined at 100 K by means of x-ray diffraction as monoclinic, with space group P 2{sub 1}, with Z=8. The crystal undergoes two structural phase transitions: one of first-order type, reversible, at 241/243 K (on cooling/heating respectively) and one of weakly first-order type, irreversible, at 277 K (on heating). The crystal dynamics is discussed on the basis of the temperature dependence of the {sup 1}H nuclear magnetic resonance second moment (M{sub 2}) and spin-lattice relaxation time T{sub 1}. Both phase transitions are interpreted in terms of the changes in the motional state of (4-apyH){sup +} cations and ClO{sub 4}- anions. The dielectric dispersion studies disclose a relaxation process over the high-temperature phase (above 241 K) in the audio-frequency region. The dielectric results are described by a Cole-Cole equation. The title crystal reveals pyroelectric properties below 241 K. The ferroelastic domain structure of (4-apyH)ClO{sub 4} is observed over the whole temperature range studied. (author)

  19. Iodine-deficient vegetarians: a hypothetical perchlorate-susceptible population?

    Science.gov (United States)

    Fields, Cheryl; Dourson, Michael; Borak, Jonathan

    2005-06-01

    Recent risk assessments of environmental perchlorate have been subject to much debate. A particular concern is whether appropriate susceptible sub-populations have been identified. Iodine-deficient pregnant women, especially vegetarians, have been proposed as such a potential susceptible sub-population, but there is no evidence of iodine deficiency in the US population and the adequacy of iodine nutrition has not been studied in US vegetarians. To understand the possibility that US vegetarians might be iodine deficient, we reviewed the prevalence, demography, and lifestyle characteristics of US vegetarians as well as the world literature on iodine nutrition in vegetarians. Our findings indicate that strict vegetarians and vegans, who comprise probably less than 0.1% of the US population, have higher education, higher incomes, and healthier lifestyles than the general population. Field studies indicate that vegetarian diets need not lead to iodine deficiency and vegans may suffer excess iodine intake. It is remains uncertain whether there are iodine-deficient vegans or pregnant women in the US. Of more general concern is whether the 10-fold default uncertainty factor is needed for intraspecies (i.e., within human) variability to protect such hypothetical susceptible sub-populations. PMID:15896441

  20. Chlorine-36 abundance in natural and synthetic perchlorate

    Energy Technology Data Exchange (ETDEWEB)

    Heikoop, Jeffrey M [Los Alamos National Laboratory; Dale, M [NON LANL; Sturchio, Neil C [UNIV OF ILLIONOIS; Caffee, M [PURDUE UNIV; Belosa, A D [UNIV OF ILLINOIS; Heraty, Jr., L J [UNIV OF ILLINOIS; Bohike, J K [RESTON, VA; Hatzinger, P B [SHAW ENIVIORNMENTAL C0.; Jackson, W A [TEXAS TECH; Gu, B [ORNL

    2009-01-01

    Perchlorate (ClO{sub 4}{sup -}) is ubiquitous in the environment. It occurs naturally as a product of atmospheric photochemical reactions, and is synthesized for military, aerospace, and industrial applications. Nitrate-enriched soils of the Atacama Desert (Chile) contain high concentrations of natural ClO{sub 4}{sup -}; nitrate produced from these soils has been exported worldwide since the mid-1800's for use in agriculture. The widespread introduction of synthetic and agricultural ClO{sub 4}{sup -} into the environment has complicated attempts to understand the geochemical cycle of ClO{sub 4}{sup -}. Natural ClO{sub 4}{sup -} samples from the southwestern United States have relatively high {sup 36}Cl abundances ({sup 36}Cl/Cl = 3,100 x 10{sup -15} to 28,800 x 10{sup -15}), compared with samples of synthetic ({sup 36}Cl/Cl = 0.0 x 10{sup -15} to 40 x 10{sup -15}) and Atacama Desert ({sup 36}Cl/Cl = 0.9 x 10{sup -15} to 590 x 10{sup -15}) ClO{sub 4}{sup -}. These data give a lower limit for the initial {sup 36}Cl abundance of natural ClO{sub 4}{sup -} and provide temporal and other constraints on its geochemical cycle.

  1. Hydrogen oxidation on gold electrode in perchloric acid solution

    Energy Technology Data Exchange (ETDEWEB)

    Sustersic, M.G.; Almeida, N.V.; Von Mengershausen, A.E. [Facultad de Ingenieria y Ciencias Economico Sociales, Universidad Nacional de San Luis, 25 de Mayo N 384, 5730 Villa Mercedes, San Luis (Argentina)

    2010-06-15

    The aim of this research is to study the interface gold/perchloric acid solution in presence of hydrogen. The reactive is generated by H{sup +} ion reduction and by saturating the electrolyte with the gaseous H{sub 2}. No evidence of H{sub 2} dissociative adsorption is found. In special conditions, a strongly adsorbed layer is formed from the atoms diffusing from inside of the metal. The mass transport occurs in three ways: the diffusion of H atoms inwards, the diffusion of H atoms back to the surface and the dissolved H{sub 2} diffusion from the bulk electrolyte to the surface. When dissolved H{sub 2} reacts, the reaction is kinetically controlled when the H{sub 2} partial pressure is high, and it is diffusionally controlled when the reactive partial pressure is low. Above 0.7 V, (measured vs. RHE), the (100) plane surface reconstruction lifts, and the rate determining step is the H diffusion towards inside of the metal, and the current suddenly falls. The Hydrogen redox reaction on gold shows reversibility with respect to the potential when the reactives are the H diffusing outwards of the metal and the H{sup +} ion present in the electrolyte. However, the absolute current values of oxidation and reduction are different because the reactive sources are different. (author)

  2. Widespread occurrence of (per)chlorate in the Solar System

    Science.gov (United States)

    Jackson, W. Andrew; Davila, Alfonso F.; Sears, Derek W. G.; Coates, John D.; McKay, Christopher P.; Brundrett, Maeghan; Estrada, Nubia; Böhlke, J. K.

    2015-11-01

    Perchlorate (ClO4-) and chlorate (ClO3-) are ubiquitous on Earth and ClO4- has also been found on Mars. These species can play important roles in geochemical processes such as oxidation of organic matter and as biological electron acceptors, and are also indicators of important photochemical reactions involving oxyanions; on Mars they could be relevant for human habitability both in terms of in situ resource utilization and potential human health effects. For the first time, we extracted, detected and quantified ClO4- and ClO3- in extraterrestrial, non-planetary samples: regolith and rock samples from the Moon, and two chondrite meteorites (Murchison and Fayetteville). Lunar samples were collected by astronauts during the Apollo program, and meteorite samples were recovered immediately after their fall. This fact, together with the heterogeneous distribution of ClO4- and ClO3- within some of the samples, and their relative abundance with respect to other soluble species (e.g., NO3-) are consistent with an extraterrestrial origin of the oxychlorine species. Our results, combined with the previously reported widespread occurrence on Earth and Mars, indicate that ClO4- and ClO3- could be present throughout the Solar System.

  3. Microbial Community Structure during Nitrate and Perchlorate Reduction in Ion-exchange Brine Using the Hydrogen-based membrane Biofilm Reactor (MBIR)

    Science.gov (United States)

    Detoxification of perchlorate by microbial communities under denitrifying conditions has been recently reported, although the identity of the mixed populations involved in perchlorate reduction is not well understood. In order to address this, the bacterial diversity of membrane ...

  4. NOVEL ASSOCIATIONS BETWEEN URINARY PERCHLORATE AND POTENTIALLY RELEVANT EFFECTS ON RISK FACTORS FOR HEART DISEASE BASED ON NHANES 2001-2002

    Science.gov (United States)

    Perchlorate is a widespread environmental pollutant, and is a thyroid hormone disruptor. A previous population study based on the National Health and Nutrition Examination Survey (NHANES) 2001-2002 database showed that urinary perchlorate concentrations were associated with signi...

  5. Adaptive evolution of Desulfovibrio alaskensis G20 for developing resistance to perchlorate

    Science.gov (United States)

    Mehta-Kolte, M. G.; Youngblut, M.; Redford, S.; Gregoire, P.; Carlson, H. K.; Coates, J. D.

    2015-12-01

    Due to its toxic, explosive, and corrosive nature, inadvertent biological H2S production by sulfate reducing microorganisms (SRM) poses significant health and industrial operational risks. Anthropogenic sources are dominated by the oil industry where H2S in reservoir gases and fluids has an associated annual cost estimated at $90 billion globally. Our previous studies have identified perchlorate (ClO4-) as a selective and potent inhibitor of SRM in pure culture and complex microbial ecosystems. However, constant addition of inhibitors like perchlorate to natural ecosystems may result in a new adaptive selective pressure on SRM populations. With this in mind we investigated the ability of Desulfovibrio alaskensis G20, a model oil reservoir SRM, to adapt to perchlorate and develop a resistance. Serial transfers of three parallel cultures with increasing concentrations of perchlorate up to 100 mM were generated and compared to wild-type strains that were transferred for same number of generations in absence of perchlorate. Genome sequencing revealed that all three adapted strains had single non-synonymous single-nucleotide polymorphisms in the same gene, Dde_2265, the sulfate adenylytransferase (ATP sulfurylase (ATPS)) (EC 2.7.7.4). ATPS catalyzes the first committed step in sulfate reduction and is essential in all SRM. IC50s against growth for these evolved strains demonstrated a three-fold increased resistance to perchlorate compared to wild-type controls. These evolved strains also had 5x higher transcriptional abundance of Dde_2265 compared to the wild-type strain. Biochemical characterization of the purified ATPS enzyme from both wild-type and the evolved strain showed that the mutant ATPS from the evolved strain was resistant to perchlorate inhibition of ATP turnover with a KI for perchlorate that was 3x greater relative to the wild-type ATPS. These results demonstrate that a single-base pair mutation in ATPS can have a significant impact on developing

  6. Permeation of chromium salts through human skin in vitro

    DEFF Research Database (Denmark)

    Gammelgaard, Bente; Fullerton, A; Avnstorp, C;

    1992-01-01

    of the dichromate solution. Chromium skin levels increased with increasing concentrations of applied chromium salts up to 0.034 M Cr. The amount of chromium in recipient phase and skin layers increased with increasing pH when the applied solution contained potassium dichromate. This was ascribed to a decreased skin...... barrier function of the skin. The amount of chromium found in all skin layers after application of chromium chloride decreased with increasing pH due to lower solubility of the salt. The % of chromium found in the recipient phase as chromium(VI) increased with increasing total chromium concentration...... indicating a limited reduction ability of the skin in vitro....

  7. Effects of lanthanum nitrate on growth and chlorophyll fluorescence characteristics of Alternanthera philoxeroides under perchlorate stress

    Institute of Scientific and Technical Information of China (English)

    谢寅峰; 蔡贤雷; 刘伟龙; 陶功胜; 陈倩; 张强

    2013-01-01

    To investigate the effects of exogenous lanthanum (La) on Alternanthera philoxeroides (Mart.) Griseb under perchlorate stress, changes in the growth and physiological parameters were investigated in solution culture experiments under controlled condi-tions. Different concentrations of La (NO3)3 were used in our study. It was shown that 0.1 and 0.5 mg/L La3+alleviated the inhibition effect of perchlorate on A. philoxeroides, including relative growth yield, dry weight of different organs, leaf area and root activity. And La3+prevented decline in the relative chlorophyll content and chlorophyll fluorescence parameters including Fv/Fm, Fv'/Fm',ΦPSI and ETR induced by perchlorate stress. Moreover, 0.5 mg/L La3+showed an optimal mitigative effect, while excess La3+(5.0 mg/L) led to synergistic effect on stress. Correlation analysis revealed a significant positive relationship between growth indexes and the chlorophyll fluorescence parameters, root activity and relative chlorophyll content (p<0.05). The results suggested that appropriate concentration of La3+could effectively alleviate growth inhibition and injury of A. philoxeroides caused by perchlorate stress, and the mitigative effect of La3+might be achieved by improving root activity, maintaining chlorophyll content and promoting photochemical efficiency of photosystem II of A. philoxeroides under perchlorate stress.

  8. Perchlorate and Nitrate Remediation Efficiency and Microbial Diversity in a Containerized Wetland Bioreactor

    Energy Technology Data Exchange (ETDEWEB)

    Jr., B D; Dibley, V; Pinkart, H; Legler, T

    2004-06-09

    We have developed a method to remove perchlorate (14 to 27 {micro}g/L) and nitrate (48 mg/L) from contaminated groundwater using a wetland bioreactor. The bioreactor has operated continuously in a remote field location for more than two years with a stable ecosystem of indigenous organisms. This study assesses the bioreactor for long-term perchlorate and nitrate remediation by evaluating influent and effluent groundwater for reduction-oxidation conditions and nitrate and perchlorate concentrations. Total community DNA was extracted and purified from 10-g sediment samples retrieved from vertical coring of the bioreactor during winter. Analysis by denaturing gradient gel electrophoresis of short, 16S rDNA, polymerase-chain-reaction products was used to identify dominant microorganisms. Bacteria genera identified were closely affiliated with bacteria widely distributed in soils, mud layers, and fresh water. Of the 17 dominant bands sequenced, most were gram negative and capable of aerobic or anaerobic respiration with nitrate as the terminal electron acceptor (Pseudomonas, Acinetobacter, Halomonas, and Nitrospira). Several identified genera (Rhizobium, Acinetobactor, and Xanthomonas) are capable of fixing atmospheric nitrogen into a combined form (ammonia) usable by host plants. Isolates were identified from the Proteobacteria class, known for the ability to reduce perchlorate. Initial bacterial assessments of sediments confirm the prevalence of facultative anaerobic bacteria capable of reducing perchlorate and nitrate in situ.

  9. Assessment of perchlorate-reducing bacteria in a highly polluted river.

    Science.gov (United States)

    Vigliotta, Giovanni; Motta, Oriana; Guarino, Francesco; Iannece, Patrizia; Proto, Antonio

    2010-11-01

    A 1-year monitoring experiment of the Sarno River basin was conducted during 2008 to evaluate the overall quality of the water over time and to compare the results with those obtained previously. The physico-chemical and microbiological characteristics of the water course had not changed appreciably with respect to previous determinations, thus emphasizing the major contribution of untreated urban wastewater to the overall pollution of the river. Moreover, attention was paid to the perchlorate ion, one of the so-called emerging contaminants, which is widespread in natural environments and is known to have adverse effects on the human thyroid gland. Over the entire monitoring program, we did not find appreciable levels of perchlorate, although the particular environmental condition could support its development. Thus, a dedicated study was designed to assess the presence of bacteria that can reasonably reduce perchlorate levels. By enrichment and molecular procedures, we identified α- and β-Proteobacteria strains, classified by 16S rDNA sequences as Dechlorospirillum sp. and Dechlorosoma sp., respectively. Further physiologic characterization and the presence of the alpha subunit gene (pcrA) of the perchlorate reductase in both strains confirmed the presence in the river of viable and active perchlorate dissimilatory bacteria. PMID:20843743

  10. Surface modification of silver nanofilms for improved perchlorate detection by surface-enhanced Raman scattering.

    Science.gov (United States)

    Hao, Jumin; Han, Mei-Juan; Li, Jinwei; Meng, Xiaoguang

    2012-07-01

    Surface-enhanced Raman scattering (SERS), as one of the most sensitive spectroscopic analysis methods, has been investigated extensively for the detection of environmental contaminants in recent years. In this work, we reported the new development of robust SERS substrates for rapid and sensitive sensing of aqueous perchlorate, a widespread environmental contaminant. The fabrication of the substrates consisted of two simple steps: (a) formation of Ag nanofilms on Cu and surface-roughened Cu foils (Ag/Cu and Ag/rCu nanofilms) using a controllable and inexpensive one-step electroless plating process, and (b) surface modification of the Ag nanofilms with cysteamine (Cys) self-assembly monolayer (SAM) (Cys-Ag/Cu and Cys-Ag/rCu substrates). Due to the strong affinity of -NH(3)(+) groups of the Cys molecules for perchlorate ions, the rapid SERS detection of perchlorate has been realized with a limit of detection (LOD) down to 5 μg L(-1) (ppb) for aqueous samples without need for drying. Various calibration curves with good linear relationships were obtained, indicating the quantification potential of SERS analysis of perchlorate using these new substrates. It was found that the neutral pH yielded the maximum SERS signals, and 85% of original sensitivity was remained in 5 days of storage time in the air, indicating the substrates are fairly stable. Within 10 regeneration-reuse cycles, the SERS signals of perchlorate kept in the range of 85-105% of the original value, verifying its reusability. PMID:22494687

  11. Simple and direct estimation chromium in different grades of steels using UV-visible spectrophotometer and associated measurement uncertainties

    International Nuclear Information System (INIS)

    Chromium is one of the important elements that provide desirable strength to different grades of steels which are chosen as structural materials for upcoming fast breeder reactors. Therefore its estimation is an important part of qualification of steels for desired applications. Several methods have been cited in literature for the estimation of chromium in steels which include most sophisticated instruments like XRFS, spark based OES, UV-Visible spectrophotometer and also classical volumetric titration. Being surface based techniques, both XRFS and spark OES have their own limitations of using matrix matching standards apart from usage of high cost instrumentation. Similarly, volumetric method being time consuming one and also the method cited in involves cumbersome chemical treatment to convert entire chromium in to measurable form of Cr (VI) and subsequent measurement by UV-Visible Spectrophotometer at 350 nm or 373 nm. As this method involves time consuming sample preparation step, it is also not a preferred method for an industrial laboratory where high analytical loads normally exists and quick analytical feedback is an issue. In view of limitations in the method cited above, an attempt has been made to develop a simple and direct method for estimation of chromium in different grades of steels containing chromium in the range of 4.75%-26%. Further, present paper also evaluates the measurement uncertainty (MU) in measurement of chromium in different grades of steels. The developed method involves the dissolution of steel in aqua-regia followed by perchloric acid fuming to convert total chromium to Cr (VI) and subsequent measurement at 447 nm after adding phosphoric acid to the suitable aliquot taken from stock solution. Phosphoric acid is added to mask iron present in solution. For the purpose to quantify measurement uncertainty, the methodology as given in EURACHEM/CITAC guide CG-4 has been followed. The expanded uncertainty at 95% confidence limit is

  12. Chromium in aqueous nitrate plutonium process streams: Corrosion of 316 stainless steel and chromium speciation

    International Nuclear Information System (INIS)

    This study was undertaken to determine if chromium(+6) could exist in plutonium process solutions under normal operating conditions. Four individual reactions were studied: the rate of dissolution of stainless steel, which is the principal source of chromium in process solutions; the rate of oxidation of chromium(+3) to chromium(+6) by nitric acid; and the reduction of chromium(+6) back to chromium(+3) by reaction with stainless steel and with oxalic acid. The stainless steel corrosion rate was found to increase with increasing nitric acid concentration, increasing hydrofluoric acid concentration, and increasing temperature. Oxidation of chromium(+3) to chromium(+6) was negligible at room temperature and only became significant in hot concentrated nitric acid. The rate of reduction of chromium(+6) back to chromium(+3) by reaction with stainless steel or oxalic acid was found to be much greater than the rate of the reverse oxidation reaction. Based on these findings and taking into account normal operating conditions, it was determined that although there would be considerable chromium in plutonium process streams it would rarely be found in the (+6) oxidation state and would not exist in the (+6) state in the final process waste solutions

  13. Activation energies involved in isothermal dehydration and decomposition of gamma-irradiated magnesium perchlorate (Paper No. RE-23)

    International Nuclear Information System (INIS)

    Gamma-irradiation enhances the acceleratory rate of dehydration as well as decomposition of magnesium perchlorate. Activation energies computed using Arrhenius treatment decreased with rise in radiation dose prior to its thermal dehydration and decomposition. The reduction in the activation energies may be attributed to the strain and stress produced in voids of the samples of magnesium perchlorate due to irradiation. (author)

  14. Alkane dehydrogenation over supported chromium oxide catalysts

    NARCIS (Netherlands)

    Weckhuysen, B.M.; Schoonheydt, R.A.

    1999-01-01

    The dehydrogenation of alkanes over supported chromium oxide catalysts in the absence of oxygen is of high interest for the industrial production of propene and isobutene. In this review, a critical overview is given of the current knowledge nowadays available about chromium-based dehydrogenation ca

  15. Martian Chlorine Chemistry: A Study of Perchlorate on the Martian Surface, Evidence of an Ongoing Formation Mechanism and Implications of a Complex Chlorine Cycle

    Science.gov (United States)

    Carrier, Brandi L.

    2015-10-01

    The research presented herein addresses the detection of perchlorate on Mars, evidence of perchlorate in Mars meteorite EETA 79001, determination of the perchlorate parent salts at the Phoenix landing site, and the ongoing formation of perchlorate from chloride minerals as well as from other oxychlorine species. The detection of perchlorate in three samples by the Phoenix Wet Chemistry Laboratory and the implication of these results are discussed. The further detection of perchlorate in Mars meteorite EETA 79001 by ion chromatography and the determination of the parent salts of the perchlorate detected at the Phoenix landing site by electrochemical analyses and ion chromatography are detailed and the implications of the identity of the parent salts are discussed. The possible formation pathways for martian perchlorate are then explored and a possible mechanism for ongoing perchlorate formation on the martian surface is detailed. Perchlorate is shown to be formed upon exposure of chloride minerals, as well as of chlorite and chlorate salts, to current Mars relevant conditions including temperature, pressure, ultraviolet radiation and atmospheric composition. The implications of this ongoing perchlorate formation for the survival and detection of organics, the oxidizing nature of the soil, formation of liquid brines and recurring slope lineae are discussed. Further preliminary experiments have been conducted to investigate the effects of perchlorate formation on the survival and degradation of organic compounds.

  16. A simplified method for obtaining high-purity perchlorate from groundwater for isotope analyses.

    Energy Technology Data Exchange (ETDEWEB)

    vonKiparski, G; Hillegonds, D

    2011-04-04

    Investigations into the occurrence and origin of perchlorate (ClO{sub 4}{sup -}) found in groundwater from across North America have been sparse until recent years, and there is mounting evidence that natural formation mechanisms are important. New opportunities for identifying groundwater perchlorate and its origin have arisen with the utilization of improved detection methods and sampling techniques. Additionally, application of the forensic potential of isotopic measurements has begun to elucidate sources, potential formation mechanisms and natural attenuation processes. Procedures developed appear to be amenable to enable high precision stable isotopic analyses, as well as lower precision AMS analyses of {sup 36}Cl. Immediate work is in analyzing perchlorate isotope standards and developing full analytical accuracy and uncertainty expectations. Field samples have also been collected, and will be analyzed when final qa/qc samples are deemed acceptable.

  17. The effect of various reaction parameters on bioremediation of perchlorate-contaminated water

    International Nuclear Information System (INIS)

    The bioremediation was employed to treat perchlorate-contaminated water. All enrichments and growth of mixed cultures were performed in anaerobic acetate medium. Enrichment cultures were started with activated sludge obtained from a local wastewater treatment plant where it predominantly treats domestic wastewater. Several parameters affecting perchlorate removal were examined through batch experiments, these include the amount of domesticated sludge, the acetate concentration, pH, the C/N ratio and the reaction temperature. The results indicated that acetate was an effective carbon source and electron donor. Under the selected conditions, namely 1.0 g domesticated sludge, an acetate concentration of 1.2 g l-1, pH 8.0, a C/N ratio of 20 at 40 deg, C, 50 mg l-1 perchlorate could be rapidly reduced to non-detectable levels within 24 h

  18. Dracorhodin perchlorate induces the apoptosis of glioma cells.

    Science.gov (United States)

    Chen, Xin; Luo, Junjie; Meng, Linghu; Pan, Taifeng; Zhao, Binjie; Tang, Zhen-Gang; Dai, Yongjian

    2016-04-01

    Dracorhodin perchlorate (Dp), a synthetic analogue of the antimicrobial anthocyanin red pigment, has recently been shown to induce apoptotic cell death in various types of cancer cells. Yet, the inhibitory effect of Dp on human glioma cells remains uninvestigated. Therefore, in the present study, 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide (MTT) assay and flow cytometry were used to detect cell viability and cell cycle progression in glioma U87MG and T98G cells, respectively. Annexin V-FITC/propidium iodide double staining and JC-1 staining were separately applied to determine cellular apoptosis and mitochondrial membrane potential damage in the cells. The expression levels of associated proteins involved in cell cycle progression and apoptosis were measured by western blotting. The activities of caspase‑9/-3 were determined by Caspase-Glo-9/3 assay. The results indicated that Dp treatment significantly inhibited cell proliferation in a dose- and time-dependent manner, and blocked cell cycle progression at the G1/S phase in the U87MG and T98G cells via the upregulation of p53 and p21 protein expression, and simultaneous downregulation of Cdc25A, Cdc2 and P-Cdc2 protein expression. Additionally, Dp treatment led to the loss of cellular mitochondrial membrane potential, and the release of cytochrome c, and strongly induced the occurence of apoptosis. Increased expression levels of Bim and Bax protein and the downregulated expression of Bcl-2 protein were observed. Caspase-9/-3 were activated and their activities were elevated after Dp treatment. These findings indicate that Dp inhibits cell proliferation, induces cell cycle arrest and apoptosis in glioma cells, and is a possible candidate for glioma treatment. PMID:26846469

  19. Microbial perchlorate reduction with elemental sulfur and other inorganic electron donors.

    Science.gov (United States)

    Ju, Xiumin; Sierra-Alvarez, Reyes; Field, Jim A; Byrnes, David J; Bentley, Harold; Bentley, Richard

    2008-03-01

    ClO(4)(-) has recently been recognized as a widespread contaminant of surface and ground water. This research investigated chemolithotrophic perchlorate reduction by bacteria in soils and sludges utilizing inorganic electron-donating substrates such as hydrogen, elemental iron, and elemental sulfur. The bioassays were performed in anaerobic serum bottles with various inocula from anaerobic or aerobic environments. All the tested sludge inocula were capable of reducing perchlorate with H2 as electron donor. Aerobic activated sludge was evaluated further and it supported perchlorate reduction with Fe(0) and S(0) additions under anaerobic conditions. Heat-killed sludge did not convert ClO(4)(-), confirming the reactions were biologically catalyzed. ClO(4)(-) (3mM) was almost completely removed by the first sampling time on d 8 with H2 (> or = 0.37mMd(-1)), after 22d with S(0) (0.18mM d(-1)) and 84% removed after 37d with Fe(0) additions (0.085mMd(-1)). Perchlorate-reduction occurred at a much faster rate (1.12mMd(-1)), when using an enrichment culture developed from the activated sludge with S(0) as an electron donor. The enrichment culture also utilized S(2-) and S(2)O(3)(2-) as electron-donating substrates to support ClO(4)(-) reduction. The mixed cultures also catalyzed the disproportionation of S(0) to S(2-) and SO(4)(2-). Evidence is presented demonstrating that S(0) was directly utilized by microorganisms to support perchlorate-reduction. In all the experiments, ClO(4)(-) was stoichiometrically converted to chloride. The study demonstrates that microorganisms present in wastewater sludges can readily use a variety of inorganic compounds to support perchlorate reduction. PMID:17988714

  20. Effects of larval-juvenile treatment with perchlorate and co-treatment with thyroxine on zebrafish sex ratios

    Science.gov (United States)

    Mukhi, S.; Torres, L.; Patino, R.

    2007-01-01

    The objective of this study was to determine the effect of larval-juvenile exposure to perchlorate, a thyroid hormone synthesis inhibitor, on the establishment of gonadal sex ratios in zebrafish. Zebrafish were exposed to untreated water or water containing perchlorate at 100 or 250 ppm for a period of 30 days starting at 3 days postfertilization (dpf). Recovery treatments consisted of a combination of perchlorate and exogenous thyroxine (T4; 10 nM). Thyroid histology was assessed at the end of the treatment period (33 dpf), and gonadal histology and sex ratios were determined in fish that were allowed an additional 10-day period of growth in untreated water. As expected, exposure to perchlorate caused changes in thyroid histology consistent with hypothyroidism and these effects were reversed by co-treatment with exogenous T4. Perchlorate did not affect fish survival but co-treatment with T4 induced higher mortality. However, relative to the corresponding perchlorate concentration, co-treatment with T4 caused increased mortality only at a perchlorate concentration of 100 ppm. Perchlorate alone or in the presence of T4 suppressed body length at 43 dpf relative to control values. Perchlorate exposure skewed the sex ratio toward female in a concentration-dependent manner, and co-treatment with T4 not only blocked the feminizing effect of perchlorate but also overcompensated by skewing the sex ratio towards male. Moreover, co-treatment with T4 advanced the onset of spermatogenesis in males. There was no clear association between sex ratios and larval survival or growth. We conclude that endogenous thyroid hormone plays a role in the establishment of gonadal sex phenotype during early development in zebrafish. ?? 2006 Elsevier Inc. All rights reserved.

  1. A low cost igniter utilizing an SCB and titanium sub-hydride potassium perchlorate pyrotechnic

    Science.gov (United States)

    Bickes, R. W., Jr.; Grubelich, M. C.; Hartman, J. K.; McCampbell, C. B.; Churchill, J. K.

    1994-01-01

    A conventional NSI (NASA Standard Initiator) normally employs a hot-wire ignition element to ignite ZPP (zirconium potassium perchlorate). With minor modifications to the interior of a header similar to an NSI device to accommodate an SCB (semiconductor bridge), a low cost initiator was obtained. In addition, the ZPP was replaced with THKP (titanium sub-hydride potassium perchlorate) to obtain increased overall gas production and reduced static-charge sensitivity. This paper reports on the all-fire and no-fire levels obtained and on a dual mix device that uses THKP as the igniter mix and a thermite as the output mix.

  2. Linking methane oxidation with perchlorate reduction: a microbial base for possible Martian life

    Science.gov (United States)

    Miller, L. G.; Carlstrom, C.; Baesman, S. M.; Coates, J. D.; Oremland, R. S.

    2011-12-01

    Recent observations of methane (CH4) and perchlorate (ClO4-) within the atmosphere and surface of Mars, respectively, provide impetus for establishing a metabolic linkage between these compounds whereby CH4 acts as an electron donor and perchlorate acts as an electron acceptor. Direct linkage through anaerobic oxidation of methane (AOM) has not been observed. However, indirect syntrophic oxygenase-dependent oxidation of CH4 with an aerobic methane oxidizer is feasible. The pathway for anaerobic dissimilatory perchlorate reduction includes 3 steps. The first 2 are sequential reductions of (1) perchlorate to chlorate and (2) chlorate to chlorite, mediated by perchlorate reductase. The third step is disproportionation of chlorite to chloride and molecular oxygen, mediated by chlorite dismutase. Utilization of thusly derived oxygen by hydrocarbon-degrading organisms in anoxic environments was first demonstrated by Coates et. al. (1998)1, however the link to aerobic methane oxidation was not examined at that time. Here, we systematically explore the potential for several species of aerobic methanotrophs to couple with chlorite during dissimilatory perchlorate reduction. In one experiment, 0.5 kPa CH4 was completely removed in one day from the headspace of combined cell suspensions of Dechloromonas agitata strain CKB and Methylococcus capsulatus in the presence of 5 mM chlorite. Oxidation of labeled 14CH4 to 14CO2 under similar conditions was later confirmed. Another experiment demonstrated complete removal of 0.2 kPa CH4 over several days by Methylobacter albus strain BG8 with strain CKB in the presence of 5 mM chlorite. Finally, we observed complete removal of 0.2 kPa CH4 in bottles containing natural soil (enriched in methanotrophs by CH4 additions over several weeks) and strain CKB and in the presence of 10 mM chlorite. This soil, collected from a pristine lake shoreline, demonstrated endogenous methane, perchlorate, chlorate and chlorite uptake. Other soil and

  3. Neutron scattering and models: Chromium

    International Nuclear Information System (INIS)

    Differential neutron elastic-scattering cross sections of elemental chromium are measured from 4.5 ∼ 10 MeV in steps of ∼ 0.5 MeV and at ≥ 40 scattering angles distributed between ∼ 17 degree--160 degree. Concurrently differential cross sections for the inelastic neutron excitation of the yrast 2+ (1.434 MeV) level in d52Cr are determined. In addition, broad inelastically-scattered neutron groups are observed corresponding to composite excitation of levels up to ∼ 5.5 MeV in the various chromium isotopes. These experimental results are combined with low-energy values previously reported from this laboratory, with recent ∼ 8 → 15 MeV data measured at the Physikalisch-Technische Bundesanstalt and with a 21.6 MeV result from the literature to form an extensive neutron-scattering data base which is interpreted in the context of spherical-optical and coupled-channels (rotational and vibrational) models. These models reasonably describe the observables but indicate rather large energy-dependent parameter trends at low energies similar to those previously reported near the peak of the So strength function in studies at this laboratory. The physical implications of the measurements and models are discussed including deformation, coupling, dispersive and asymmetry effects

  4. Chemical Stability of Chromium Carbide and Chromium Nitride Powders Compared with Chromium Metal in Synthetic Biological Solutions

    OpenAIRE

    Tao Jiang; Inger Odnevall Wallinder; Gunilla Herting

    2012-01-01

    Chromium carbide (Cr-C) and chromium nitride (Cr-N) powders were compared with a chromium metal powder (Cr-metal) to evaluate their chemical stability in solution. All three powders were exposed in five different synthetic biological solutions of varying pH and chemical composition simulating selected human exposure conditions. Characterisation of the powders, using GI-XRD, revealed that the predominant bulk crystalline phases were Cr7C3 and Cr2N for Cr-C and Cr-N respectively. The outermost ...

  5. Low-chromium reduced-activation chromium-tungsten steels

    Energy Technology Data Exchange (ETDEWEB)

    Klueh, R.L.; Alexander, D.J.; Maziasz, P.J. [Oak Ridge National Lab., TN (United States)

    1996-10-01

    Bainitic microstructures formed during continuous cooling can differ from classical upper and lower bainite formed during isothermal transformation. Two types of non-classical bainite were observed depending on the cooling rate: carbide-free acicular bainite at rapid cooling rates and granular bainite at slower cooling rates. The Charpy impact toughness of the acicular ferrite was found to be considerably better than for the granular bainite. It was postulated that alloying to improve the hardenability of the steel would promote the formation of acicular bainite, just as increasing the cooling rate does. To test this, chromium and tungsten were added to the 2 1/4Cr-2W and 2 1/4Cr-2WV steel compositions to increase their hardenability, and the microstructures and mechanical properties were examined.

  6. Bainitic chromium-tungsten steels with 3 pct chromium

    International Nuclear Information System (INIS)

    Previous work on 3Cr-1.5MoV (nominally Fe-3Cr-2.5Mo-0.25V-0.1C), 2.25Cr-2W (Fe-2.25Cr-2W-0.1C), and 2.25Cr-2WV (Fe-2.25Cr-2W-0.25V-0.1C) steels indicated that the impact toughness of these steels depended on the microstructure of the bainite formed during continuous cooling from the austenization temperature. Microstructures formed during continuous cooling can differ from classical upper and lower bainite formed during isothermal transformation. Two types of nonclassical microstructures were observed depending on the cooling rate: carbide-free acicular bainite at rapid cooling rates and granular bainite at slower cooling rates. The Charpy impact toughness of the acicular ferrite was considerably better than for the granular bainite. It was postulated that alloying to improve the hardenability of the steel would promote the formation of acicular bainite, just as increasing the cooling rate does. To test this, chromium and tungsten were added to the 2.25Cr-2W and 2.25Cr-2WV steel compositions to increase their hardenability. Charpy testing indicated that the new 3Cr-W and 3Cr-WV steels had improved impact toughness, as demonstrated by lower ductile-brittle transition temperatures and higher upper-shelf energies. This improvement occurred with less tempering than was necessary to achieve similar toughness for the 2.25Cr steels and for high-chromium (9 to 12 pct Cr) Cr-W and Cr-Mo steels

  7. Reproductive toxicological aspects of chromium in males

    International Nuclear Information System (INIS)

    To expand our present understanding of the effects of chromium on male fertility a number of studies were designed to achieve this through the use of chromium intoxicated experimental animals and through investigation of sexual hormones and sperm quality in welders. Also in view of the lack of an experimental model for effects of noxious substance on the epididymal spermatozoa the main objectives of the series of studies reviewed here were: A. To establish a model for evaluation of epididymal sperm count and motility in the rat. B. To investigate and compare the effects of tri- and hexavalent chromium on epididymal spermatozoa. Further to describe the effects of low-dose long-time exposure of rats to the most toxicological interesting chromium oxidative state - hexavalent chromium. C. By the use of autoradiography and γ-countinuing to expand the present knowledge on the distribution of chromium in the body with special reference to the male reproductive organs. D. To describe the effects of exposure to hexavalent chromium in welding fume on levels of sexual hormones and semen parameters in welders. (EG)

  8. Synthesis of Chromium (Ⅲ) 5-aminosalicylate

    Institute of Scientific and Technical Information of China (English)

    LI Wei; HAO Er-jun; JIANG Yu-qin

    2004-01-01

    As we all known that diabetes is a chronic disease with major health consequences.Research has revealed that the occurrence of diabetes have great thing to do with the chromium deficient. Almost 40 years after the first report of glucose tolerance factor(GTF) [1], no conclusive evidence for an isolable ,biologically active form of chromium exited. Three materials have been proposed to be the biologically active form of chromium: "glucose tolerance factor", chromium Picolinate and low-molecular-weight chromium-binding substance (LWMCr) [2] . So there is potential for the design of new chromium drugs .5-Aminosalicylic acid (5-ASA) is identified as an active component in the therapy of inflammatory bowel disease (IBD) such as Crohn's disease and ulcerative colitis . The therapeutic action of 5-ASA is believed to be coupled to its ability to act as a free radical scavenger [3-4],acting locally on the inflamed colonic mucosa [5-7]. However, the clinical use of 5-ASA is limited, since orally administered 5-ASA is rapidly and completely absorbed from the upper gastrointestinal tract and therefore the local therapeutic effects of 5-ASA in the colon is hardly expected.In this paper, we report the synthesis of chromium(Ⅲ)5-aminosalicylate from 5-ASA and CrCl3. 6H2O.The synthesis route is as follow:The complex has been characterized by elemental analysis, IR spectra, X-ray powder diffractionand TG-DTA . They indicate that the structure is tris(5-ASA) Chromium . Experiments show that thecomplex has a good activity for supplement tiny dietary chromium, lowering blood glucose levels,lowering serum lipid levels and in creasing lean body mass .

  9. Chromium in leather footwear-risk assessment of chromium allergy and dermatitis

    DEFF Research Database (Denmark)

    Thyssen, Jacob P; Strandesen, Maria; Poulsen, Pia B;

    2012-01-01

    Background. Chromium-tanned leather footwear, which releases >3 ppm hexavalent Cr(VI), may pose a risk of sensitizing and eliciting allergic dermatitis. Objectives. To determine the content and potential release of chromium in leather footwear and to discuss the prevention of chromium contact...... allergy and dermatitis. Methods. Sixty pairs of leather shoes, sandals and boots (20 children's, 20 men's, and 20 women's) were purchased in Copenhagen and examined with X-ray fluorescence spectroscopy. Chromium was extracted according to the International Standard, ISO 17075. The detection level for Cr......(VI) was 3 ppm. Results. Chromium was identified in 95% of leather footwear products, the median content being 1.7% (range 0-3.3%). No association with store category or footwear category was found. A tendency for there to be a higher chromium content in footwear with high prices was shown (p(trend) = 0...

  10. Characteristics of chromium-allergic dermatitis patients prior to regulatory intervention for chromium in leather

    DEFF Research Database (Denmark)

    Bregnbak, David; Thyssen, Jacob P; Zachariae, Claus;

    2014-01-01

    BACKGROUND: Chromium-tanned leather articles currently constitute the most important cause of contact allergy to chromium in Denmark. A regulation on the content of hexavalent chromium in leather was adopted in November 2013 by the EU member states. OBJECTIVES: To characterize patients with...... chromium allergy and their disease, to serve as a baseline for future studies on the potential effect of the new regulation on chromium in leather. METHODS: A questionnaire case-control study was performed on 155 dermatitis patients with positive patch test reactions to potassium dichromate and a matched...... control group of 621 dermatitis patients. Comparisons were made by use of a χ(2) -test and the Mann-Whitney U-test. Logistic regression analyses were used to test for associations. RESULTS: Sixty-six per cent of chromium-allergic patients had a positive history of contact dermatitis caused by leather...

  11. High Pressure Burn Rate Measurements on an Ammonium Perchlorate Propellant

    Energy Technology Data Exchange (ETDEWEB)

    Glascoe, E A; Tan, N

    2010-04-21

    High pressure deflagration rate measurements of a unique ammonium perchlorate (AP) based propellant are required to design the base burn motor for a Raytheon weapon system. The results of these deflagration rate measurements will be key in assessing safety and performance of the system. In particular, the system may experience transient pressures on the order of 100's of MPa (10's kPSI). Previous studies on similar AP based materials demonstrate that low pressure (e.g. P < 10 MPa or 1500 PSI) burn rates can be quite different than the elevated pressure deflagration rate measurements (see References and HPP results discussed herein), hence elevated pressure measurements are necessary in order understand the deflagration behavior under relevant conditions. Previous work on explosives have shown that at 100's of MPa some explosives will transition from a laminar burn mechanism to a convective burn mechanism in a process termed deconsolidative burning. The resulting burn rates that are orders-of-magnitude faster than the laminar burn rates. Materials that transition to the deconsolidative-convective burn mechanism at elevated pressures have been shown to be considerably more violent in confined heating experiments (i.e. cook-off scenarios). The mechanisms of propellant and explosive deflagration are extremely complex and include both chemical, and mechanical processes, hence predicting the behavior and rate of a novel material or formulation is difficult if not impossible. In this work, the AP/HTPB based material, TAL-1503 (B-2049), was burned in a constant volume apparatus in argon up to 300 MPa (ca. 44 kPSI). The burn rate and pressure were measured in-situ and used to calculate a pressure dependent burn rate. In general, the material appears to burn in a laminar fashion at these elevated pressures. The experiment was reproduced multiple times and the burn rate law using the best data is B = (0.6 {+-} 0.1) x P{sup (1.05{+-}0.02)} where B is the burn

  12. Chromium intensification of a processed dental radiograph

    International Nuclear Information System (INIS)

    This study was undertaken to determine (1) the usefulness of chromium intensifier to improve the diagnostic quality of light radiograph; (2) the effect of chromium intensifier on density contrast; and (3) the effect of various chemical concentrations on density. The following results obtained: 1. CHROMIUM INTENSIFIER is useful for intensifying and improving the diagnostic quality of a light dental radiograph. 2. The degree of intensification can be controlled by varying bleaching time, repeating the processing, varying the proportions of the potassium bicarbonate and hydrochloric acid solutions. 3. The image produced is black and permanent. 4. The intensifier increases density and contrast

  13. Chromium (VI) adsorption on boehmite

    Energy Technology Data Exchange (ETDEWEB)

    Granados-Correa, F. [Instituto Nacional de Investigaciones Nucleares, Apartado Postal 18-1027 Col., Escandon, Delegacion Miguel Hidalgo, C.P. 11801 Mexico, D.F. (Mexico)], E-mail: fgc@nuclear.inin.mx; Jimenez-Becerril, J. [Instituto Nacional de Investigaciones Nucleares, Apartado Postal 18-1027 Col., Escandon, Delegacion Miguel Hidalgo, C.P. 11801 Mexico, D.F. (Mexico)

    2009-03-15

    Boehmite was synthesized and characterized in order to study the adsorption behavior and the removal of Cr(VI) ions from aqueous solutions as a function of contact time, initial pH solution, amount of adsorbent and initial metal ion concentration, using batch technique. Adsorption data of Cr(VI) on the boehmite were analyzed according to Freundlich, Langmuir and Dubinin-Radushkevich (D-R) adsorption models. Thermodynamic parameters for the adsorption system were determinated at 293, 303, 313 and 323 K temperatures. The kinetic values and thermodynamic parameters from the adsorption process show that the Cr(VI) ions adsorption on boehmite is an endothermic and spontaneous process. These results show that the boehmite could be considered as a potential adsorbent for chromium ions in aqueous solutions.

  14. Chromium – An essential mineral

    Directory of Open Access Journals (Sweden)

    Merlin D Lindemann

    2009-09-01

    Full Text Available The status of chromium (Cr is not a new question. Cr is clearly an essential nutrient; this is a position that has been held for over three decades by individual scientists, groups of scientists, and governmental committees. The most uniform response across species with regard to Cr deficiency symptoms that are responsive to Cr supplementation are alterations in glucose metabolism with special reference to peripheral tissue sensitivity to insulin. Because the body’s ability to control blood glucose is critical to many life functions, and loss of ability to adequately control blood glucose can lead to many health debilitations, a consequence of Cr supplementation can be improved health and reproductive outcomes as well as improved survival rate or life span.

  15. Occupational asthma due to chromium.

    Science.gov (United States)

    Leroyer, C; Dewitte, J D; Bassanets, A; Boutoux, M; Daniel, C; Clavier, J

    1998-01-01

    We describe a 28-year-old subject employed as a roofer in a construction company since the age of 19, who developed work-related symptoms of a cough, shortness of breath, wheezing, rhinitis and headaches. A description of a usual day at work suggested that the symptoms worsened while he was sawing corrugated fiber cement. Baseline spirometry was normal, and there was a mild bronchial hyperresponsiveness to carbachol. A skin patch test to chromium was negative. A specific inhalation challenge showed a boderline fall in forced expiratory volume in 1 s (FEV1) after exposure to fiber cement dust. Exposure to nebulization of potassium dichromate (K2Cr2O7), at 0.1 mg.ml-1 for 30 min, was followed by an immediate fall by 20% FEV1. Simultaneously, a significant increase in bronchial hyperresponsiveness was demonstrated. PMID:9782225

  16. Chromium isotope uptake in carbonates

    DEFF Research Database (Denmark)

    Rodler, Alexandra

    Chromium (Cr) is a redox sensitive element potentially capable of tracing fine-scale fluctuations of the oxygenation of Earth’s early surface environments and seawater. The Cr isotope composition of carbonates could perhaps be used as paleo-redox proxy to elucidate changes in the geological past....... Processes that potentially fractionate Cr isotopes, perhaps during deposition, burial and alteration need to be constrained.Previous studies have shown that Cr isotopes are fractionated during oxidative weathering on land, where heavy Cr isotopes are preferentially removed with Cr(VI) while residual soils...... retain an isotopically light Cr signature. Cr(VI) enriched in heavy Cr isotopes is then transported via river waters to the oceans and sequestered into marine sediments. Marine chemical sediments such asbanded iron formations and modern marine carbonates have proven useful in recording the Cr isotope...

  17. A steady-state biofilm model for simultaneous reduction of nitrate and perchlorate, part 1: model development and numerical solution.

    Science.gov (United States)

    Tang, Youneng; Zhao, Heping; Marcus, Andrew K; Krajmalnik-Brown, Rosa; Rittmann, Bruce E

    2012-02-01

    A multispecies biofilm model is developed for simultaneous reduction of nitrate and perchlorate in the H(2)-based membrane biofilm reactor. The one-dimension model includes dual-substrate Monod kinetics for a steady-state biofilm with five solid and five dissolved components. The solid components are autotrophic denitrifying bacteria, autotrophic perchlorate-reducing bacteria, heterotrophic bacteria, inert biomass, and extracellular polymeric substances (EPS). The dissolved components are nitrate, perchlorate, hydrogen (H(2)), substrate-utilization-associated products, and biomass-associated products (BAP). The model explicitly considers four mechanisms involved in how three important operating conditions (H(2) pressure, nitrate loading, and perchlorate loading) affect nitrate and perchlorate removals: (1) competition for H(2), (2) promotion of PRB growth due to having two electron acceptors (nitrate and perchlorate), (3) competition between nitrate and perchlorate reduction for the same resources in the PRB: electrons and possibly reductase enzymes, and (4) competition for space in the biofilm. Two other special features are having H(2) delivered from the membrane substratum and solving directly for steady state using a novel three-step approach: finite-difference for approximating partial differential and/or integral equations, Newton-Raphson for solving nonlinear equations, and an iterative scheme to obtain the steady-state biofilm thickness. An example result illustrates the model's features. PMID:22191376

  18. A STUDY ON THE ACCUMULATION OF PERCHLORATE IN YOUNG HEAD LETTUCE

    Science.gov (United States)

    The overall objective of this study was to demonstrate in a greenhouse study the potential for incorporation of perchlorate from aqueous solutions of 10, 50, 100, 500, 1,000, 5,000, and 10,000 ppb into an agricultural food crop (lettuce; Lactuca sativa), which is typically grown ...

  19. (Per)chlorate reduction by an acetogenic bacterium, Sporomusa sp., isolated from an underground gas storage.

    KAUST Repository

    Balk, Melike

    2010-08-03

    A mesophilic bacterium, strain An4, was isolated from an underground gas storage reservoir with methanol as substrate and perchlorate as electron acceptor. Cells were Gram-negative, spore-forming, straight to curved rods, 0.5-0.8 microm in diameter, and 2-8 microm in length, growing as single cells or in pairs. The cells grew optimally at 37 degrees C, and the pH optimum was around 7. Strain An4 converted various alcohols, organic acids, fructose, acetoin, and H(2)/CO(2) to acetate, usually as the only product. Succinate was decarboxylated to propionate. The isolate was able to respire with (per)chlorate, nitrate, and CO(2). The G+C content of the DNA was 42.6 mol%. Based on the 16S rRNA gene sequence analysis, strain An4 was most closely related to Sporomusa ovata (98% similarity). The bacterium reduced perchlorate and chlorate completely to chloride. Key enzymes, perchlorate reductase and chlorite dismutase, were detected in cell-free extracts.

  20. ISSUES IN MANAGING THE RISKS ASSOCIATED WITH PERCHLORATE IN DRINKING WATER

    Science.gov (United States)

    Perchlorate (ClO4-) contamination of ground and surface waters has placed drinking water supplies at risk in communities throughout the US, especially in the West. Several major assessment studies of that risk in terms of health and environmental impact are ...

  1. Trace determination of perchlorate using electromembrane extraction and capillary electrophoresis with capacitively coupled contactless conductivity detection

    Czech Academy of Sciences Publication Activity Database

    Kiplagat, I.K.; Doan, T.K.O.; Kubáň, Pavel; Boček, Petr

    2011-01-01

    Roč. 32, č. 21 (2011), s. 3008-3015. ISSN 0173-0835 R&D Projects: GA ČR GAP206/10/1219 Institutional research plan: CEZ:AV0Z40310501 Keywords : electromembrane extraction * perchlorate * capillary electrophoresis Subject RIV: CB - Analytical Chemistry, Separation Impact factor: 3.303, year: 2011

  2. (Per)chlorate reduction by an acetogenic bacterium, Sporomusa sp., isolated from an underground gas storage.

    Science.gov (United States)

    Balk, Melike; Mehboob, Farrakh; van Gelder, Antonie H; Rijpstra, W Irene C; Damsté, Jaap S Sinninghe; Stams, Alfons J M

    2010-09-01

    A mesophilic bacterium, strain An4, was isolated from an underground gas storage reservoir with methanol as substrate and perchlorate as electron acceptor. Cells were Gram-negative, spore-forming, straight to curved rods, 0.5-0.8 microm in diameter, and 2-8 microm in length, growing as single cells or in pairs. The cells grew optimally at 37 degrees C, and the pH optimum was around 7. Strain An4 converted various alcohols, organic acids, fructose, acetoin, and H(2)/CO(2) to acetate, usually as the only product. Succinate was decarboxylated to propionate. The isolate was able to respire with (per)chlorate, nitrate, and CO(2). The G+C content of the DNA was 42.6 mol%. Based on the 16S rRNA gene sequence analysis, strain An4 was most closely related to Sporomusa ovata (98% similarity). The bacterium reduced perchlorate and chlorate completely to chloride. Key enzymes, perchlorate reductase and chlorite dismutase, were detected in cell-free extracts. PMID:20680263

  3. Periodate salts as pyrotechnic oxidizers: development of barium- and perchlorate-free incendiary formulations.

    Science.gov (United States)

    Moretti, Jared D; Sabatini, Jesse J; Chen, Gary

    2012-07-01

    In a flash: pyrotechnic incendiary formulations with good stabilities toward various ignition stimuli have been developed without the need for barium or perchlorate oxidizers. KIO(4) and NaIO(4) were introduced as pyrotechnic oxidizers and exhibited excellent pyrotechnic performance. The periodate salts may garner widespread use in military and civilian fireworks because of their low hygroscopicities and high chemical reactivities. PMID:22639415

  4. Developmental exposure to perchlorate alters synaptic transmission in hippocampus of the adult rat.

    Science.gov (United States)

    The Food Quality Protection Act and Safe Drinking Water Act mandate the EPA to identify potential health risks associated with chemicals that act on the endocrine system. Perchlorate, a contaminant found in food and water supplies throughout the USA, blocks iodine uptake into the...

  5. Double-Polymer-Modified Pencil Lead for Stripping Voltammetry of Perchlorate in Drinking Water

    Science.gov (United States)

    Izadyar, Anahita; Kim, Yushin; Ward, Michelle M.; Amemiya, Shigeru

    2012-01-01

    The inexpensive and disposable electrode based on a double-polymer-modified pencil lead is proposed for upper-division undergraduate instrumental laboratories to enable the highly sensitive detection of perchlorate. Students fabricate and utilize their own electrodes in the 3-4 h laboratory session to learn important concepts and methods of…

  6. DISTRIBUTION OF PERCHLORATE IN SAMPLES OF SODIUM NITRATE (CHILE SALTPETER) FERTILIZER DERIVED FROM NATURAL CALICHE

    Science.gov (United States)

    Two lots of sodium nitrate fertilizer derived from Chilean caliche were analyzed to determine the distribution of perchlorate throughout the material. Although our samples represent a limited amount, we found that distribution was essentially homogeneous in any 100-g portion. Whe...

  7. Radioiodine tracers as useful tools in studies of thyrotoxic effects of exogenous bromide and perchlorate ions

    Czech Academy of Sciences Publication Activity Database

    Pavelka, Stanislav

    2012-01-01

    Roč. 291, č. 2 (2012), s. 405-408. ISSN 0236-5731 R&D Projects: GA ČR(CZ) GA304/08/0256 Institutional research plan: CEZ:AV0Z50110509 Keywords : bromide * perchlorate * radioiodine tracer * thyroid hormone Subject RIV: ED - Physiology Impact factor: 1.467, year: 2012

  8. Preparation and Analysis of Solid Solutions in the Potassium Perchlorate-Permanganate System.

    Science.gov (United States)

    Johnson, Garrett K.

    1979-01-01

    Describes an experiment, designed for and tested in an advanced inorganic laboratory methods course for college seniors and graduate students, that prepares and analyzes several samples in the nearly ideal potassium perchlorate-permanganate solid solution series. The results are accounted for by a theoretical treatment based upon aqueous…

  9. 高氯酸诺氟沙星铜(Ⅱ)%Norfloxacin Coppe(Ⅱ) Perchlorate

    Institute of Scientific and Technical Information of China (English)

    谢永荣; 叶琼; 熊仁根

    2004-01-01

    The hydrothermal treatment of Cu(ClO4)2·6H2O and Norfloxacin (H-Norf) afforded [Cu(H-Noff)2(ClO4)2] (1) in which center Cu has a square planar geometry while perchlorate just acts as charge balance anions. CCDC:140821.

  10. Radiation decomposition of ammonium perchlorate in the presence of composite rocket propellant ingredients

    International Nuclear Information System (INIS)

    Radiolysed ammonium perchlorate (AP) oxidises aqueous iodide ions more when it is irradiated in combination with either aluminium, hydroxy terminated polybutadiene (HTPB), copper chromite or iron oxide. The influence is large in the case of AP + HTPB and AP + Copper chromite. (author)

  11. Fractionation of stable isotopes in perchlorate and nitrate during in situ biodegradation in a sandy aquifer

    Science.gov (United States)

    Hatzinger, P.B.; Böhlke, J.K.; Sturchio, N.C.; Gu, B.; Heraty, L.J.; Borden, R.C.

    2009-01-01

    Environmental context. Perchlorate (ClO4-) and nitrate (NO3-) are common co-contaminants in groundwater, with both natural and anthropogenic sources. Each of these compounds is biodegradable, so in situ enhanced bioremediation is one alternative for treating them in groundwater. Because bacteria typically fractionate isotopes during biodegradation, stable isotope analysis is increasingly used to distinguish this process from transport or mixing-related decreases in contaminant concentrations. However, for this technique to be useful in the field to monitor bioremediation progress, isotope fractionation must be quantified under relevant environmental conditions. In the present study, we quantify the apparent in situ fractionation effects for stable isotopes in ClO4- (Cl and O) and NO3- (N and O) resulting from biodegradation in an aquifer. Abstract. An in situ experiment was performed in a shallow alluvial aquifer in Maryland to quantify the fractionation of stable isotopes in perchlorate (Cl and O) and nitrate (N and O) during biodegradation. An emulsified soybean oil substrate that was previously injected into this aquifer provided the electron donor necessary for biological perchlorate reduction and denitrification. During the field experiment, groundwater extracted from an upgradient well was pumped into an injection well located within the in situ oil barrier, and then groundwater samples were withdrawn for the next 30 h. After correction for dilution (using Br- as a conservative tracer of the injectate), perchlorate concentrations decreased by 78% and nitrate concentrations decreased by 82% during the initial 8.6 h after the injection. The observed ratio of fractionation effects of O and Cl isotopes in perchlorate (18O/37Cl) was 2.6, which is similar to that observed in the laboratory using pure cultures (2.5). Denitrification by indigenous bacteria fractionated O and N isotopes in nitrate at a ratio of ???0.8 (18O/15N), which is within the range of values

  12. Systematics of Natural Perchlorate in Precipitation, Soils, and Plants at the Amargosa Desert Research Site, Nye County, Nevada

    Science.gov (United States)

    Andraski, B. J.; Stonestrom, D. A.; Jackson, W. A.; Rajagopalan, S.; Taylor, E. M.

    2007-12-01

    Naturally occurring perchlorate is known to be associated with nitrate deposits of the hyperarid Atacama Desert in Chile, and recent large-scale sampling has identified a substantial reservoir (up to 1 kg/ha) of natural perchlorate in diverse unsaturated zones of the arid and semiarid Southwestern United States (Rao et al., 2007, ES&T, DOI: 10.1021/es062853i). The objective of the Amargosa Desert work is to develop a better understanding of the deposition, accumulation, and biological cycling of perchlorate in arid environments. Occurrence of perchlorate was evaluated by sampling shallow soil profiles up to 3 m in depth at four different locations and at two different time periods, and by sampling dominant plant species growing near the subsurface profiles. Deposition of perchlorate was evaluated by analyzing both bulk deposition (precipitation plus dry fall, collected under oil) collected on site and wet deposition samples collected by the National Atmospheric Deposition program at a nearby site. Soil samples and atmospheric-deposition samples were tested for both perchlorate (ClO4- ) and major anions. Perchlorate concentrations (0.2-20 µg/kg) were variable with depth in soil profiles and generally correlated most highly with chloride (Cl-) and nitrate (NO3-), although the intensity of these relations differed among profiles. Plant concentrations were generally above 1 mg/kg, suggesting ClO4- accumulation. Concentrations of ClO4- were generally much greater in total deposition than wet deposition samples, indicating a substantial dryfall component of meteoric deposition. This presentation will present the mass distribution and variability of perchlorate in bulk deposition, soils, and plants. Reasons for observed relations between subsurface concentrations of perchlorate and other anions will be explored.

  13. Simultaneous determination of chromium(III) and chromium(VI) in aqueous solutions by ion chromatography and chemiluminescence detection

    DEFF Research Database (Denmark)

    Gammelgaard, Bente; Jøns, O; Nielsen, B

    1992-01-01

    A method for the simultaneous determination of chromium(iii) and chromium(vi) in a flow system based on chemiluminescence was developed. A Dionex cation-exchange guard column was used to separate chromium(iii) from chromium(vi), and chromium(vi) was reduced by potassium sulfite, whereupon both sp....... The detection limit was 0.5 micrograms l-1 for both species. Data were in agreement with Zeeman-effect background corrected atomic absorption spectrometry measurements....

  14. AEROSOL BEHAVIOR IN CHROMIUM WASTE INCINERATION

    Institute of Scientific and Technical Information of China (English)

    Suyuan Yu

    2003-01-01

    Cr2O3 is considered as the dominant incineration product during the combustion disposal of chromium waste. A hydrogen/air diffusion flame was employed to simulate the industrial process of incineration. Cr2O3 aerosols were generated inside the flame by the gas phase reaction of chromium and oxygen. Chromium came from the rapid decomposition of chromium hexacarbonyl (Cr(CO)6) at room temperature and was carried into the combustion chamber by hydrogen. Aerosol and clusters can then be easily formed in the flame by nucleation and coagulation. A two dimensional Discrete-Sectional Model (DSM) was adopted to calculate the Cr2O3 aerosol behavior. The experimental measurement method was Dynamic Light Scattering. The numerically predicted results agreed well with those of the experimental measurement. Both results show that the Cr2O3 aerosol size reached about 70 nanometers at the flame top.

  15. Potentiometry: A Chromium (III) -- EDTA Complex

    Science.gov (United States)

    Hoppe, J. I.; Howell, P. J.

    1975-01-01

    Describes an experiment that involves the preparation of a chromium (III)-EDTA compound, a study of its infrared spectrum, and the potentiometric determination of two successive acid dissociation constants. (Author/GS)

  16. Bioremediation of chromium solutions and chromium containing wastewaters.

    Science.gov (United States)

    Malaviya, Piyush; Singh, Asha

    2016-08-01

    Cr(VI) represents a serious threat to human health, living resources and ecological system as it is persistent, carcinogenic and toxic, whereas, Cr(III), another stable oxidation state of Cr, is less toxic and can be readily precipitated out of solution. The conventional methods of Cr(VI) removal from wastewaters comprise of chemical reduction followed by chemical precipitation. However, these methods utilize large amounts of chemicals and generate toxic sludge. This necessitates the need for devising an eco-technological strategy that would use the untapped potential of the biological world for remediation of Cr(VI) containing wastewaters. Among several viable approaches, biotransformation of Cr(VI) to relatively non-toxic Cr(III) by chromium resistant bacteria offers an economical- and environment-friendly option for its detoxification. Various studies on use of Cr(VI) tolerant viable bacterial isolates for treatment of Cr(VI) containing solutions and wastewater have been reported. Therefore, a detailed account of mechanisms and processes involved in bioreduction of Cr(VI) from solutions and wastewaters by bacterial isolates are the focus of this review article in addition to a discussion on toxicity of Cr(VI) on bacterial strains and various factors affecting Cr(VI) bioreduction. PMID:25358056

  17. Diminishing Chromium Use on Combined Chromium-Gambier Tanning Process Upon the Characteristics of Tanned Leather

    Directory of Open Access Journals (Sweden)

    A. Kasim

    2014-04-01

    Full Text Available The research was aimed to investigate the influence of minimizing chromium use on combined chromium-gambier process upon the characteristics of tanned leather. At the first stage of tanning process, chromium was used and in the second stage it was replaced by gambier. The raw material used was dried saline-preserved goat skin. The treatments applied on the tanning process were the different concentrations of chromium ranging from the highest level of 6% to the lowest level of 1% which was then re-tanned by using 8% concentration of gambier. The examination parameters included chemical and physical properties as well as visual investigation on the tanned leather in accordance with SNI-06-0463-1989-A. The result showed that the tanning process by using 2% chromium in the first step and 8% gambier in the second step was a treatment combination producing tanned leather that met the standard. The examination on tanned leather resulted from such treatment showed 56.33% rawhide, 17.45% of bound tannin, 31.22% of tanning level, tensile strength 386.30 kg/cm2, flexibility 31.91%, leather width 1.3 mm, density 0.75 g/cm3, the leather was quite elastic with light brownish color. In conclusion, minimizing the use of chromium in the combined tanning process of chromium and gambier can be implemented to the lowest of 2% chromium concentration and 8% gambier in the first and second step, respectively.

  18. Dissimilatory perchlorate reduction linked to aerobic methane oxidation via chlorite dismutase

    Science.gov (United States)

    Oremland, R. S.; Baesman, S. M.; Miller, L. G.

    2013-12-01

    The presence of methane (CH4) in the atmosphere of Mars is controversial yet the evidence has aroused scientific interest, as CH4 could be a harbinger of extant or extinct microbial life. There are various oxidized compounds present on the surface of Mars that could serve as electron acceptors for the anaerobic oxidation of CH4, including perchlorate (ClO4-). We examined the role of perchlorate, chlorate (ClO3-) and chlorite (ClO2-) as oxidants linked to CH4 oxidation. Dissimilatory perchlorate reduction begins with reduction of ClO4- to ClO2- and ends with dismutation of chlorite to yield chloride (Cl-) and molecular oxygen (O2). We explored the potential for aerobic CH4 oxidizing bacteria to couple with oxygen derived from chlorite dismutation during dissimilatory perchlorate reduction. Methane (0.2 kPa) was completely removed within several days from the N2-flushed headspace above cell suspensions of methanotrophs (Methylobacter albus strain BG8) and perchlorate reducing bacteria (Dechloromonas agitata strain CKB) in the presence of 5 mM ClO2-. Similar rates of CH4 consumption were observed for these mixed cultures whether they were co-mingled or segregated under a common headspace, indicating that direct contact of cells was not required for methane consumption to occur. We also observed complete removal of 0.2 kPa CH4 in bottles containing dried soil (enriched in methanotrophs by CH4 additions over several weeks) and D. agitata CKB and in the presence of 10 mM ClO2-. This soil (seasonally exposed sediment) collected from the shoreline of a freshwater lake (Searsville Lake, CA) demonstrated endogenous CH4 uptake as well as perchlorate, chlorate and chlorite reduction/dismutation. However, these experiments required physical separation of soil from the aqueous bacterial culture to allow for the partitioning of O2 liberated from chlorite dismutation into the shared headspace. Although dissimilatory reduction of ClO4- and ClO3- could be inferred from the

  19. Lateral stress evolution in chromium sulfide cermets with varying excess chromium

    Science.gov (United States)

    Petel, O. E.; Appleby-Thomas, G. J.; Wood, D. C.; Capozzi, A.; Nabavi, A.; Goroshin, S.; Frost, D. L.; Hazell, P. J.

    2016-04-01

    The shock response of chromium sulfide-chromium, a cermet of potential interest as a matrix material for ballistic applications, has been investigated at two molar ratios. Using a combustion synthesis technique allowed for control of the molar ratio of the material, which was investigated under near-stoichiometric (cermet) and excess chromium (interpenetrating composite) conditions, representing chromium:sulfur molar ratios of 1.15:1 and 4:1, respectively. The compacts were investigated via the plate-impact technique, which allowed the material to be loaded under a one-dimensional state of strain. Embedded manganin stress gauges were employed to monitor the temporal evolution of longitudinal and lateral components of stress in both materials. Comparison of these two components has allowed assessment of the variation of material shear strength both with impact pressure/strain-rate and time for the two molar ratio conditions. The two materials exhibited identical material strength despite variations in their excess chromium contents.

  20. Physiological and genetic description of dissimilatory perchlorate reduction by the novel marine bacterium Arcobacter sp. strain CAB.

    Science.gov (United States)

    Carlström, Charlotte I; Wang, Ouwei; Melnyk, Ryan A; Bauer, Stefan; Lee, Joyce; Engelbrektson, Anna; Coates, John D

    2013-01-01

    A novel dissimilatory perchlorate-reducing bacterium (DPRB), Arcobacter sp. strain CAB, was isolated from a marina in Berkeley, CA. Phylogenetically, this halophile was most closely related to Arcobacter defluvii strain SW30-2 and Arcobacter ellisii. With acetate as the electron donor, strain CAB completely reduced perchlorate (ClO4(-)) or chlorate (ClO3(-)) [collectively designated (per)chlorate] to innocuous chloride (Cl(-)), likely using the perchlorate reductase (Pcr) and chlorite dismutase (Cld) enzymes. When grown with perchlorate, optimum growth was observed at 25 to 30°C, pH 7, and 3% NaCl. Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) preparations were dominated by free-swimming straight rods with 1 to 2 polar flagella per cell. Strain CAB utilized a variety of organic acids, fructose, and hydrogen as electron donors coupled to (per)chlorate reduction. Further, under anoxic growth conditions strain CAB utilized the biogenic oxygen produced as a result of chlorite dismutation to oxidize catechol via the meta-cleavage pathway of aerobic catechol degradation and the catechol 2,3-dioxygenase enzyme. In addition to (per)chlorate, oxygen and nitrate were alternatively used as electron acceptors. The 3.48-Mb draft genome encoded a distinct perchlorate reduction island (PRI) containing several transposases. The genome lacks the pcrC gene, which was previously thought to be essential for (per)chlorate reduction, and appears to use an unrelated Arcobacter c-type cytochrome to perform the same function. IMPORTANCE The study of dissimilatory perchlorate-reducing bacteria (DPRB) has largely focused on freshwater, mesophilic, neutral-pH environments. This study identifies a novel marine DPRB in the genus Arcobacter that represents the first description of a DPRB associated with the Campylobacteraceae. Strain CAB is currently the only epsilonproteobacterial DPRB in pure culture. The genome of strain CAB lacks the pcrC gene found in all

  1. Determination of perchlorate in drinking water by ion chromatography using macrocycle-based concentration and separation methods.

    Science.gov (United States)

    Lamb, John D; Simpson, David; Jensen, Bryce D; Gardner, Joseph S; Peterson, Quinn P

    2006-06-16

    Macrocycle-based ion chromatography provides a convenient, reliable method for the determination of perchlorate ion, which is currently of great interest to the environmental community. This study shows that effective perchlorate determinations can be made using standard conductimetric detection by combining an 18-crown-6-based mobile phase with an underivatized reversed-phase mobile phase ion chromatography (MPIC) column. One unique feature of this method is the flexibility in column capacity that is achieved through simple variations in eluent concentrations of 18-crown-6 and KOH, facilitating the separation of target analyte anions such as perchlorate. Using a standard anion exchange column as concentrator makes possible the determination of perchlorate as low as 0.2 ug/L in low ionic strength matrices. Determination of perchlorate at the sub-ug/L level in pure water and in spiked local city hard water samples with high background ion concentrations can be achieved this way. However, like other IC techniques, this method is challenged to achieve analyses at the ug/L level in the demanding high ionic strength matrix described by the United States Environmental Protection Agency (EPA) (1,000 mg/L chloride, sulfate and carbonate). We approached this challenge by use of the Cryptand C1 concentrator column, provided by Dionex Corporation, to effectively preconcentrate perchlorate while reducing background ion concentrations in the high ionic strength matrix. The retention characteristics of the concentrator column were studied in order to maximize its effectiveness for perchlorate determinations. The method makes possible the determination of perchlorate at the 5 ug/L level in the highest ionic strength matrix described by the EPA. PMID:16516902

  2. Perchlorate content of plant foliage reflects a wide range of species-dependent accumulation but not ozone-induced biosynthesis

    International Nuclear Information System (INIS)

    Perchlorate (ClO4−) interferes with uptake of iodide in humans. Emission inventories do not explain observed distributions. Ozone (O3) is implicated in the natural origin of ClO4−, and has increased since pre-industrial times. O3 produces ClO4−in vitro from Cl−, and plant tissues contain Cl− and redox reactions. We hypothesize that O3 exposure may induce plant synthesis of ClO4−. We exposed contrasting crop species to environmentally relevant O3 concentrations. In the absence of O3 exposure, species exhibited a large range of ClO4− accumulation but there was no relationship between leaf ClO4− and O3, whether expressed as exposure or cumulative flux (dose). Older, senescing leaves accumulated more ClO4− than younger leaves. O3 exposed vegetation is not a source of environmental ClO4−. There was evidence of enhanced ClO4− content in the soil surface at the highest O3 exposure, which could be a significant contributor to environmental ClO4−. -- Highlights: • Exposure to ozone in crop species does not induce accumulation nor biosynthesis of perchlorate. • Older leaves accumulate more perchlorate than younger leaves. • Soil surface may accumulate perchlorate following exposure to ozone. • Species differ greatly in accumulation of perchlorate from the rhizosphere, independent of ozone. • Ozone exposed vegetation is not a candidate source of environmental perchlorate. -- Exposure of crop species to ozone did not lead to biosynthesis or greater accumulation of foliar perchlorate. Older leaves accumulated more perchlorate than younger leaves

  3. Oxygen and chlorine isotopic fractionation during perchlorate biodegradation: Laboratory results and implications for forensics and natural attenuation studies

    Science.gov (United States)

    Sturchio, N.C.; Böhlke, J.K.; Beloso, A.D., Jr.; Streger, S.H.; Heraty, L.J.; Hatzinger, P.B.

    2007-01-01

    Perchlorate is a widespread environmental contaminant having both anthropogenic and natural sources. Stable isotope ratios of O and Cl in a given sample of perchlorate may be used to distinguish its source(s). Isotopic ratios may also be useful for identifying the extent of biodegradation of perchlorate, which is critical for assessing natural attenuation of this contaminant in groundwater. For this approach to be useful, however, the kinetic isotopic fractionations of O and Cl during perchlorate biodegradation must first be determined as a function of environmental variables such as temperature and bacterial species. A laboratory study was performed in which the O and Cl isotope ratios of perchlorate were monitored as a function of degradation by two separate bacterial strains (Azospira suillum JPLRND and Dechlorospirillum sp. FBR2) at both 10??C and 22??C with acetate as the electron donor. Perchlorate was completely reduced by both strains within 280 h at 22??C and 615 h at 10??C. Measured values of isotopic fractionation factors were ??18O = -36.6 to -29.0??? and ??37Cl = -14.5 to -11.5???, and these showed no apparent systematic variation with either temperature or bacterial strain. An experiment using 18O-enriched water (??18O = +198???) gave results indistinguishable from those observed in the isotopically normal water (??18O = -8.1???) used in the other experiments, indicating negligible isotope exchange between perchlorate and water during biodegradation. The fractionation factor ratio ??18O/??37Cl was nearly invariant in all experiments at 2.50 ?? 0.04. These data indicate that isotope ratio analysis will be useful for documenting perchlorate biodegradation in soils and groundwater. The establishment of a microbial fractionation factor ratio (??18O/??37Cl) also has significant implications for forensic studies. ?? 2007 American Chemical Society.

  4. Speciation of Chromium in Water Samples with Homogeneous Liquid-Liquid Extraction and Determination by Flame Atomic Absorption Spectrometry

    International Nuclear Information System (INIS)

    A novel method was developed for the speciation of chromium in natural water samples based on homogeneous liquid-liquid extraction and determination by flame atomic absorption spectrometry (FAAS). In this method, Cr(III) reacts with a new Schiff's base ligand to form the hydrophobic complex, which is subsequently entrapped in the sediment phase, whereas Cr(VI) remained in aqueous phase. The Cr(VI) assay is based on its reduction to Cr(III) by the addition of sodium sulfite to the sample solution. Thus, separation of Cr(III) and Cr(VI) could be realized. Homogeneous liquid-liquid extraction based on the pH-independent phase-separation process was investigated using a ternary solvent system (water-tetrabutylammonium ion (TBA+)-chloroform) for the preconcentration of chromium. The phase separation phenomenon occurred by an ion-pair formation of TBA and perchlorate ion. Then sedimented phase was separated using a 100 μL micro-syringe and diluted to 1.0 mL with ethanol. The sample was introduced into the flame by conventional aspiration. After the optimization of complexation and extraction conditions such as pH = 9.5, [ligand] = 1.0 x 10-4 M, [TBA+] = 2.0 x 10-2 M, [CHCl3] = 100.0 μL and [ClO4-] = 2.0 x 10-2 M, a preconcentration factor (Va/Vs) of 100 was obtained for only 10 mL of the sample. The relative standard deviation was 2.8% (n = 10). The limit of detection was sufficiently low and lie at ppb level. The proposed method was applied for the extraction and determination of chromium in natural water samples with satisfactory results

  5. A Reservoir of Natural Perchlorate in Unsaturated Zones of Arid and Semi-Arid Regions, Southwestern USA

    Science.gov (United States)

    Rao, B. A.; Stonestrom, D. A.; Anderson, T. A.; Orris, G. J.; Rajagapolan, S.; Sandvig, R. M.; Scanlon, B. R.; Walvoord, M. A.; Jackson, W.

    2006-12-01

    Natural perchlorate (ClO4-) is generally present in unsaturated zones of steppe-to-desert regions of the arid and semi-arid southwestern United States. The perchlorate is associated with atmospherically deposited chloride that has accumulated throughout the Holocene. To assess this natural reservoir, we analyzed unsaturated-zone profiles from ten sites across Nevada, New Mexico, Texas, and Utah for perchlorate and other anions. The sampled sites represent a wide range of precipitation (0.1 0.5 m yr-1), dominant vegetation, soil type, underlying geology, and include five distinct ecological regions: Chihuahuan, Mojave, and southern Great Basin deserts; Arizona-New Mexico semi-desert; and Texas High Plains dry steppe. Concentrations of perchlorate correlated closely with chloride and bromide. The perchlorate reservoir (up to 1 kg ha-1) is sufficiently large to impact groundwater when natural recharge during pluvial periods or induced recharge after conversion to agriculture flushes accumulated salts from the unsaturated zone. This little explored source can explain perchlorate in milk and other agricultural products far from anthropogenic contamination, and should be considered when evaluating overall exposure risk.

  6. The enriched chromium neutrino source for GALLEX

    International Nuclear Information System (INIS)

    The preparation and study of an intense source of neutrinos in the form of neutron irradiated materials which are enriched in Cr-50 for use in the GALLEX solar neutrino experiment are discussed. Chromyl fluoride gas is enriched in the Cr-50 isotope by gas centrifugation and subsequently converted to a very stable form of chromium oxide. The results of neutron activation analyses of such chromium samples indicate low levels of any long-lived activities, but show that short-lived activities, in particular Na-24, may be of concern. These results show that irradiating chromium oxide enriched in Cr-50 is preferable to irradiating either natural chromium or argon gas as a means of producing a neutrino source to calibrate the GALLEX detector. These results of the impurity level analysis of the enriched chromyl fluoride gas and its conversion to the oxide are also of interest to work in progress by other members of the Collaboration investigating an alternative conversion of the enriched gas to chromium metal. 35 refs., 12 figs., 5 tabs

  7. Serum chromium levels in gestational diabetes mellitus

    Directory of Open Access Journals (Sweden)

    P G Sundararaman

    2012-01-01

    Full Text Available Objective: To measure serum chromium level in women with gestational diabetes mellitus (GDM from Chennai, South India. Materials and Methods: Thirty women with gestational diabetes, 60 age matched controls. Inclusion criteria: Gestational age 22-28 weeks, age group 20-35 years. Exclusion Criteria: Gestational age beyond 28 weeks, malnutrition or presence of infection. Serum chromium was measured using inductive couple plasma emission spectrometer. Results: Serum chromium levels of women with GDM, 1.59+/-0.02 ng/ml (range: 0.16-4.0 ng/ml were lower than in controls (4.58+/-0.62 ng/ml; range 0.82-5.33 ng/ml (P < 0.001. However, there were no significant differences among cases and controls when subdivided by parity. Conclusions: Women with GDM from a South Indian city had lower levels of serum chromium compared to pregnant women without GDM. Studies may be done whether chromium supplementation is useful in this group of women.

  8. Occupational exposure to chromium(VI compounds

    Directory of Open Access Journals (Sweden)

    Jolanta Skowroń

    2015-07-01

    Full Text Available This article discusses the effect of chromium(VI (Cr(VI on human health under conditions of acute and chronic exposure in the workplace. Chromium(VI compounds as carcinogens and/or mutagens pose a direct danger to people exposed to them. If carcinogens cannot be eliminated from the work and living environments, their exposure should be reduced to a minimum. In the European Union the proposed binding occupational exposure limit value (BOELV for chromium(VI of 0.025 mg/m³ is still associated with high cancer risk. Based on the Scientific Commitee of Occupational Exposure Limits (SCOEL document chromium(VI concentrations at 0.025 mg/m³ increases the risk of lung cancer in 2–14 cases per 1000 exposed workers. Exposure to chromium(VI compounds expressed in Cr(VI of 0.01 mg Cr(VI/m3 is responsible for the increased number of lung cancer cases in 1–6 per 1000 people employed in this condition for the whole period of professional activity. Med Pr 2015;66(3:407–427

  9. [Occupational exposure to chromium(VI) compounds].

    Science.gov (United States)

    Skowroń, Jolanta; Konieczko, Katarzyna

    2015-01-01

    This article discusses the effect of chromium(VI) (Cr(VI)) on human health under conditions of acute and chronic exposure in the workplace. Chromium(VI) compounds as carcinogens and/or mutagens pose a direct danger to people exposed to them. If carcinogens cannot be eliminated from the work and living environments, their exposure should be reduced to a minimum. In the European Union the proposed binding occupational exposure limit value (BOELV) for chromium(VI) of 0.025 mg/m³ is still associated with high cancer risk. Based on the Scientific Commitee of Occupational Exposure Limits (SCOEL) document chromium(VI) concentrations at 0.025 mg/m³ increases the risk of lung cancer in 2-14 cases per 1000 exposed workers. Exposure to chromium(VI) compounds expressed in Cr(VI) of 0.01 mg Cr(VI)/m3; is responsible for the increased number of lung cancer cases in 1-6 per 1000 people employed in this condition for the whole period of professional activity. PMID:26325053

  10. Secondary transformation mechanism of paramagnetic centers in irradiated alkali metal perchlorates

    International Nuclear Information System (INIS)

    The EPR method has been used to study thermal transformations of paramagnetic centres (PC) in X-ray irradiated potassium, rubidium and cesium perchlorates. Experimental data make it possible to suppose that diffusion coefficient of O- ion a rather high and this ion is freely diffused already at 262 K. Colliding with [MeClO4]+ centres it is transformed in a molecule of oxygen. Another part of O- is transformed in stable ozonide-ion at 300 K. About room temperature hole centres dissociate with formation of ClO2 radical. It is supposed that part of electron and hole centres is not stabilized but at 77 K it is transformed in stable radiolysis products. This process most effective proceeds in dislocations and on the surface of microcrystals. The suggested model of thermal transformations of primary PC in irradiated perchlorates of alkali metals explains formation of all the finite ion and paramagnetic radiolysis products

  11. Kinetics of oxidation of uranium(IV) by permanganate ion in aqueous perchlorate media

    International Nuclear Information System (INIS)

    The kinetics of oxidation of uranium(IV) by permanganate ion in 1.0 mol dm-3 perchloric acid solution has been investigated using a stopped-flow spectrophotometer. The reaction was found to be second order overall and first order in the concentrations of both reactants. The catalytic effect of the perchlorates of Hg2+, Cu2+, and Fe3+ on the reaction rate has been investigated. The activation parameters were evaluated and found to be ΔS not= 30.52 ± 1.22 kJ-1 mol-1, ΔH not= 62.89 ± 1.87 kJ mol-1, and ΔG not=53.79 ± 1.44 kJ mol-1. A tentative mechanism consistent with the kinetics is discussed. (author)

  12. Laboratory investigation of perchlorate deliquescence at the surface of Mars with a Raman scattering lidar

    Science.gov (United States)

    Nikolakakos, George; Whiteway, James A.

    2015-10-01

    A sample of magnesium perchlorate hexahydrate was subjected to the water vapor pressure and temperatures found at the landing site of the Phoenix Mars mission. Laser Raman scattering was applied to detect the onset of deliquescence and provide a relative estimate of the quantity of water taken up and subsequently released by the sample. As the temperature of the sample decreased at the same rate as measured on Mars during the evening, significant uptake of water from the atmosphere was observed to occur prior to the frost point temperature being reached. As the temperature was lowered further, the relative humidity over ice increased to 100% and frost formed on the surface surrounding the perchlorate sample. Freezing of the brine film was observed at the eutectic temperature of -67°C, and thawing occurred at a temperature of -62°C.

  13. trans-Tetraaquabis[bis(pyridin-3-ylmethanone-κN]manganese(II bis(perchlorate

    Directory of Open Access Journals (Sweden)

    Bin Liu

    2012-01-01

    Full Text Available In the title complex, [Mn(C11H8N2O2(H2O4](ClO42, the Mn2+ ion is located on an inversion center with the slightly distorted N2O4 octahedral coordination sphere comprising N-atom donors from two monodentate trans-related bis(pyridin-3-ylmethanone ligands and four water ligands. The two perchlorate anions are linked to the mononuclear complex molecule through water O—H...O hydrogen bonds while inter-complex water O—H...N(pyridine interactions form an infinite chain structure extending along the b axis. The perchlorate anions also function as inter-unit links through water O—H...O hydrogen bonds which, together with water O—H...O(carbonyl interactions, give a three-dimensional framework structure.

  14. Thermal behavior of aluminum powder and potassium perchlorate mixtures by DTA and TG

    International Nuclear Information System (INIS)

    In this work the thermal decomposition characteristics of micron sized aluminum powder + potassium perchlorate pyrotechnic systems were studied with thermal analytical techniques. The results show that the reactivity of aluminum powder in air increases as the particle size decreases. Pure aluminum with 5 μm particle size has a fusion temperature about 647 deg. C, but this temperature for 18 μm powder is 660 deg. C. Pure potassium perchlorate has an endothermic peak at 300 deg. C corresponding to a rhombic-cubic transition, a fusion temperature around 590 deg. C and decomposes at 592 deg. C. DTA curves for Al5/KClO4 (30:70) mixture show a maximum peak temperature for thermal decomposition at 400 deg. C. Increasing the particle size of aluminum powder increases the ignition temperature of the mixture. The oxidation temperature increased by enhance in the aluminum content of the mixture

  15. Thermal behavior of aluminum powder and potassium perchlorate mixtures by DTA and TG

    Energy Technology Data Exchange (ETDEWEB)

    Pourmortazavi, S.M. [Faculty of Material and Manufacturing Technologies, Malek Ashtar University of Technology, P.O. Box 16765-3454, Tehran (Iran, Islamic Republic of)]. E-mail: pourmortazavi@yahoo.com; Fathollahi, M. [Faculty of Material and Manufacturing Technologies, Malek Ashtar University of Technology, P.O. Box 16765-3454, Tehran (Iran, Islamic Republic of); Hajimirsadeghi, S.S. [Faculty of Material and Manufacturing Technologies, Malek Ashtar University of Technology, P.O. Box 16765-3454, Tehran (Iran, Islamic Republic of); Hosseini, S.G. [Faculty of Material and Manufacturing Technologies, Malek Ashtar University of Technology, P.O. Box 16765-3454, Tehran (Iran, Islamic Republic of)

    2006-04-01

    In this work the thermal decomposition characteristics of micron sized aluminum powder + potassium perchlorate pyrotechnic systems were studied with thermal analytical techniques. The results show that the reactivity of aluminum powder in air increases as the particle size decreases. Pure aluminum with 5 {mu}m particle size has a fusion temperature about 647 deg. C, but this temperature for 18 {mu}m powder is 660 deg. C. Pure potassium perchlorate has an endothermic peak at 300 deg. C corresponding to a rhombic-cubic transition, a fusion temperature around 590 deg. C and decomposes at 592 deg. C. DTA curves for Al{sub 5}/KClO{sub 4} (30:70) mixture show a maximum peak temperature for thermal decomposition at 400 deg. C. Increasing the particle size of aluminum powder increases the ignition temperature of the mixture. The oxidation temperature increased by enhance in the aluminum content of the mixture.

  16. Radiation-chemical behaviour of Rh(3) in perchloric and nitric acid media

    International Nuclear Information System (INIS)

    Rhodium(3) behaviour in solutions of concentrated (> 1 mol/l) nitric and perchloric acids under 60Co gamma radiation with dose rate of 3.5 Gy/s has been studied. It is shown that in case of nitrate solution irradiation by doses up to 2x104 Gy, rhodium(3) concentration does not change. Rhodium(3) proved to be stable in perchlorate solutions in case of irradiation by doses up to 3x104 Gy; however, in the presence of organic acids and alcohols its reduction to methane occurred. Kinetic characteristics of rhodium(3) reduction by ethyl alcohol by the doses up to 4x104 Gy have been ascertained, reduction mechanism being considered. 6 refs.; 4 figs.; 1 tab

  17. Flashlamp-pumped lasing of chromium-doped GSG garnet

    International Nuclear Information System (INIS)

    The implications for the practical use of chromium:GSGG in lamp-pumped tunable lasers are discussed in this paper. The authors report here some major improvements in the performance of the flashlamp-pumped chromium:GSGG laser

  18. Surface Chemistry and Spectroscopy of Chromium in Inorganic Oxides

    OpenAIRE

    Weckhuysen, B. M.; Wachs, I.E.; Schoonheydt, R. A.

    1996-01-01

    Focuses on the surface chemistry and spectroscopy of chromium in inorganic oxides. Characterization of the molecular structures of chromium; Mechanics of hydrogenation-dehydrogenation reactions; Mobility and reactivity on oxidic surfaces.

  19. Experimental investigation on the heterogeneous kinetic process of the low thermal decomposition of ammonium perchlorate particles

    Energy Technology Data Exchange (ETDEWEB)

    Longuet, Baptiste [Laboratoire Energetique Explosions et Structures Universite d' Orleans (Germany); Gillard, Philippe [Laboratoire Energetic Explosions et Structures, Universite d' Orleans, Bourges (France)

    2009-02-15

    The thermal decomposition of ammonium perchlorate has been extensively studied in the past. Nevertheless, the various results published illustrate, on the one hand, significant differences regarding the influence of different parameters on the decomposition and on the other hand, a lack of useful quantitative laws to predict the thermal behaviour of this crystal under a range of conditions (temperature, duration of exposure, presence of confinement). (Abstract Copyright [2009], Wiley Periodicals, Inc.)

  20. Electric conductivity of gel-polymeric electrolytes with Ca, Mg and Zn perchlorate salts

    OpenAIRE

    NIKOLA CVJETICANIN; SLAVKO MENTUS

    1999-01-01

    The gel-polymeric electrolytes were prepared with calcium, magnesium and zinc perchlorates dissolved in propylene carbonate together with poly (acrylo nitrile) or poly(methyl methacrylate) as a solution immobilizing polymers. The electric conductivity of these electrolytes was examined in the dependence of temperature and solvent content, at a constant salt-to-polymer concentration ratio. The electrolyte compositions were outlined having the conductivity close to 10-3 S cm-1. It was demonstra...

  1. Non-aqueous titrimetric assay of gabapentin in capsules using perchloric acid as titrant

    OpenAIRE

    Sameer A. M. Abdulrahman; KANAKAPURA BASAVAIAH

    2011-01-01

    Two simple, rapid, accurate and inexpensive methods using visual and potentiometric titrimetric techniques are described for the determination of gabapentin (GBP) in bulk drug as well as in capsules. The methods are based on the neutralization reaction of the primary amino group of GBP with acetous perchloric acid as titrant in anhydrous acetic acid medium. The end point was detected either visually using crystal violet as indicator or potentiometrically using a modified glass electrode SCE e...

  2. Electrochromic iridium oxide films: Compatibility with propionic acid, potassium hydroxide, and lithium perchlorate in propylene carbonate

    OpenAIRE

    Wen, Rui-Tao; Niklasson, Gunnar A.; Granqvist, Claes G.

    2013-01-01

    Porous thin films of It oxide were prepared by reactive dc magnetron sputtering onto unheated substrates. The crystallite size was similar to 5 nm, and a small amount of unoxidized Ir was present. The electrochromic performance was studied by optical transmittance measurements and cyclic voltammetry applied to films in aqueous and non-aqueous electrolytes, specifically being 1 M propionic acid, 1 M potassium hydroxide (KOH), and 1 M lithium perchlorate in propylene carbonate (Li-PC). Cyclic v...

  3. Disproportionation of plutonium IV in concentrated solutions of plutonium in perchloric acid

    International Nuclear Information System (INIS)

    This work was carried out to study the dependence of the PuIV disproportionation reaction in perchloric acid solution on the plutonium concentration up to 20 g/l. Solutions of such high plutonium concentration have not previously been studied. It was found that the bimolecular rate constant and the equilibrium constant of the disproportionation reaction were not appreciably different from their values at lower concentrations. (author)

  4. Radiometric quantification of thyrotoxic and goitrogenic effects of exogenous bromide and perchlorate ions

    Czech Academy of Sciences Publication Activity Database

    Pavelka, Stanislav

    Bratislava: Slovenská technická univerzita, 2012, s. 152-156. ISBN 978-80-227-3722-7. [Priemyselná toxikológia 2012 /32./. Svit, Vysoké Tatry (SK), 20.06.2012-22.06.2012] R&D Projects: GA ČR(CZ) GA304/08/0256 Institutional research plan: CEZ:AV0Z50110509 Keywords : bromide * perchlorate * radiometric assay * thyroid peroxidase Subject RIV: ED - Physiology

  5. The use of chlorate, nitrate, and perchlorate to promote crude oil mineralization in salt marsh sediments.

    Science.gov (United States)

    Brundrett, Maeghan; Horita, Juske; Anderson, Todd; Pardue, John; Reible, Danny; Jackson, W Andrew

    2015-10-01

    Due to the high volume of crude oil released by the Deepwater Horizon oil spill, the salt marshes along the gulf coast were contaminated with crude oil. Biodegradation of crude oil in salt marshes is primarily limited by oxygen availability due to the high organic carbon content of the soil, high flux rate of S(2-), and saturated conditions. Chlorate, nitrate, and perchlorate were evaluated for use as electron acceptors in comparison to oxygen by comparing oil transformation and mineralization in mesocosms consisting of oiled salt marsh sediment from an area impacted by the BP Horizon oil spill. Mineralization rates were determined by measuring CO2 production and δ (13)C of the produced CO2 and compared to transformation evaluated by measuring the alkane/hopane ratios over a 4-month period. Total alkane/hopane ratios decreased (~55-70 %) for all treatments in the following relative order: aerated ≈ chlorate > nitrate > perchlorate. Total CO2 produced was similar between treatments ranging from 550-700 mg CO2-C. The δ (13)C-CO2 values generally ranged between the indigenous carbon and oil values (-17 and -27‰, respectively). Oil mineralization was greatest for the aerated treatments and least for the perchlorate amended. Our results indicate that chlorate has a similar potential as oxygen to support oil mineralization in contaminated salt marshes, but nitrate and perchlorate were less effective. The use of chlorate as a means to promote oil mineralization in situ may be a promising means to remediate contaminated salt marshes while preventing unwanted secondary impacts related to nutrient management as in the case of nitrate amendments. PMID:25854211

  6. The Investigation of Perchlorate/Iron Phase Mixtures as A Possible Source of Oxygen Detected by the Sample Analysis at Mars (SAM) Instrument in Gale Crater, Mars

    Science.gov (United States)

    Sutter, B.; Heil, E.; Morris, R. V.; Archer, P. D.; Ming, D. W.; Niles, P. B.; Eigenbrode, J. L.; Franz, H.; Freissinet C.; Glavin, D. P.; McAdam, A. C.; Mahaffy, P.; Martin-Torres, F. Javier; Navarro-Gonzalez, R.; Paz-Zorzano, Maria; Stern, J. C.; McKay, C. P.

    2015-01-01

    The Sample Analysis at Mars (SAM) instrument onboard the Curiosity rover detected O2 and HCl gas releases from the Rocknest (RN) eolian bedform and the John Klein (JK) and Cumberland (CB) drill hole materials in Gale Crater. Chlorinated hydrocarbons have also been detected by the SAM quadrupole mass spectrometer (QMS) and gas chromatography/mass spectrometer (GCMS). These detections along with the detection of perchlorate (ClO4-) by the Mars Phoenix Lander's Wet Chemistry Laboratory (WCL) suggesting perchlorate is a possible candidate for evolved O2 and chlorine species. Laboratory thermal analysis of individual per-chlorates has yet to provide an unequivocal temperature match to the SAM O2 and HCl release data. These detections along with the detection of perchlorate (ClO4-) by the Mars Phoenix Lander's Wet Chemistry Laboratory suggested perchlorate is a possible candidate for evolved O2 and chlorine species. Laboratory thermal analysis of pure perchlorates has yet to provide an unequivocal temperature match to the SAM O2 and HCl release data. Analog laboratory analysis of iron mineralogy detected in Gale materials that was physically mixed with Ca- and Mg-perchlorate has been shown to catalyze lower O2 release temperatures and approach some SAM O2 release data. Instead of physical mixtures used in previous work, the work presented here utilized perchlorate solutions added to Fe phases. This technique allowed for perchlorate to come in closer contact with the Fe-phase and may more closely mimic Mars conditions where humidity can increase enough to cause deliquescence of the highly hygroscopic perchlorate phases. The objective of this work is to: 1) Utilize a laboratory SAM analog instrument to evaluate the O2 release temperatures from Mg- and Ca-perchlorates solutions applied to Fephases detetected in Gale Crate; and 2) Determine if perchlorate solutions can provide improved matches with the SAM O2 temperature release profiles.

  7. Evaluation of the natural attenuation potential of a complex pollution plume (chlorate, perchlorate, 1,2dichloroethane and vinyl chloride) by autochthonous microbial communities

    OpenAIRE

    Harris-Hellal, Jennifer; Joulian, Catherine; Hube, Daniel; Coulon, Stéphanie; Guérin, Valérie; Garrido, Françis

    2013-01-01

    Artificially synthetized chloride-based-oxyanions such as perchlorate (ClO4-) and chlorate (ClO3-), are used in a vast number of applications such as military and aerospace industry; they are also used as herbicides and in pyrotechnic applications. Due to their very high solubility, perchlorate and chlorate are readily transported in water systems and can thus end up in drinking water. Ingestion of perchlorate may affect iodine uptake by the human thyroid and thus thyroidal hormone production...

  8. Studies of Some Novel Chromium Pyridine Dicarboxylate Complexes

    OpenAIRE

    Chauhan Jayprakash S; Patel Rameshchandra P; Pandya Ajit V

    2014-01-01

    Chromium pyridine di-carboxylate complexes are synthesized from Chromium (III) with pyridine 2, 6- dicarboxylic acid, pyridine 2, 3 and 2, 5- dicarboxylic acids. Chromium forms colored complexes. Chromium (III) forms a violate complex with pyridine 2, 6- dicarboxylic acid and purple violate complex with pyridine 2, 3 and 2, 5- dicarboxylic acids. The job’s method indicates metal ligand ratio to be 1:2. The interpretation of UV-VIS spectra indicates octahedral geometry and IR spectra give clue...

  9. Kinetics of thermal decomposition of nano magnesium oxide catalyzed ammonium perchlorate

    International Nuclear Information System (INIS)

    Arrhenius kinetic parameters of ammonium perchlorate (AP) catalyzed with nano-sized magnesium oxide (MgO) has been determined in this work. Nano particles of MgO with an average size of approximately 20 to 30 nm have been used to catalyze the AP. The particles were characterized using Scanning electron microscope (SEM) and X-ray diffraction (XRD) techniques before mixing with AP. Simultaneous Thermal Analysis (STA) shows that MgO nanoparticles have a strong catalytic effect on the thermal decomposition of ammonium perchlorate. The addition of MgO nano particles reduces the two stage decomposition of ammonium perchlorate to a single stage. Arrhenius kinetic parameters of pure and the catalyzed AP have been calculated using non isothermal kinetic approach based on Kissinger method. The comparison of the thermal behavior and kinetic parameters of pure and catalyzed AP has also been carried out to elucidate the reaction mechanism. The results show that the activation energy of the catalyzed AP has increased from 138.1 kJ/mole to 159.1kJ/mole. The rate of reaction, however, has increased in the catalyzed AP showing that it has become more reactive by the addition of MgO nano particles. The enthalpy of activation has increased by 16 percent in the catalyzed AP. (author)

  10. Perchlorate induced low temperature carbonate decomposition in the Mars Phoenix Thermal and Evolved Gas Analyzer (TEGA)

    Science.gov (United States)

    Cannon, K. M.; Sutter, B.; Ming, D. W.; Boynton, W. V.; Quinn, R.

    2012-07-01

    Simulated Thermal Evolved Gas Analyzer (TEGA) analyses have shown that a CO2 release detected between 400°C and 680°C by the Phoenix Lander's TEGA instrument may have been caused by a reaction between calcium carbonate and hydrated magnesium perchlorate. In our experiments a CO2 release beginning at 385 ± 12°C was attributed to calcite reacting with water vapor and HCl gas from the dehydration and thermal decomposition of Mg-perchlorate. The release of CO2 is consistent with the TEGA detection of CO2 released between 400 and 680°C, with the amount of CO2 increasing linearly with added perchlorate. X-ray diffraction (XRD) experiments confirmed CaCl2 formation from the reaction between calcite and HCl. These results have important implications for the Mars Science Laboratory (MSL) Curiosity rover. Heating soils may cause inorganic release of CO2; therefore, detection of organic fragments, not CO2 alone, should be used as definitive evidence for organics in Martian soils.

  11. Temporal and spatial variation of perchlorate in streambed sediments: results from in-situ dialysis samplers

    International Nuclear Information System (INIS)

    The fate of perchlorate (ClO4-) in streambed sediments is becoming a concern due to the increasing number of groundwater and surface water contamination sites in the United States. Dialysis samplers were deployed at three sites over a period of 1 year to determine the vertical distribution of ClO4-in sediment pore water. Results indicated that the spatial and temporal ClO4-penetration into sediments could be affected by numerous factors, such as temperature, microbial degradation, ClO4-surface water concentration, and sediment physico-geological properties. In general, maximum ClO4-penetration into sediments at the studied sites was 30 cm below the sediment-water surface. The vertical sequential depletion of electron acceptors in sediments suggested that microbial reduction was responsible for ClO4-depletion in stream sediments. Biodegradation of ClO4-occurred over a seasonally variable active depth zone of 1-10 cm. Results implied that there was a rapid natural attenuation potential of perchlorate in saturated near-surface sediments. -Perchlorate may be rapidly attenuated in saturated near-surface sediments

  12. Widespread occurrence of perchlorate in water, foodstuffs and human urine collected from Kuwait and its contribution to human exposure.

    Science.gov (United States)

    Alomirah, Husam F; Al-Zenki, Sameer F; Alaswad, Marivi C; Alruwaih, Noor A; Wu, Qian; Kannan, Kurunthachalam

    2016-06-01

    Perchlorate is a thyroid hormone-disrupting compound and is reported to occur widely in the environment. Little is known on human exposure to perchlorate in Kuwait. In this study, 218 water samples, 618 commonly consumed foodstuffs and 532 urine samples collected from Kuwait were analysed to assess the exposure of the Kuwaiti population to perchlorate. For the estimation of daily intake of perchlorate, food consumption rates were obtained from the National Nutrition Survey in the State of Kuwait (NNSSK). The results showed that leafy vegetables accounted for a major share of perchlorate exposure among the Kuwaiti population at 0.062 µg kg(-)(1) bw day(-)(1) (36.2%), followed by fruits at 0.026 µg kg(-)(1) bw day(-)(1) (15.3%) and non-leafy vegetables at 0.017 µg kg(-)(1) bw day(-)(1) (10.1%). The urinary perchlorate geometric mean (GM) concentrations ranged from 8.51 to 17.1 µg l(-)(1) for the five age groups, which were higher than those reported in other countries. The estimated urinary perchlorate exposure for the Kuwaiti general population was 0.42 µg kg(-)(1) bw day(-)(1), which was higher than that reported for the United States. The dietary intake of perchlorate for the Kuwaiti population ranged from 0.14 to 0.67 µg kg(-)(1) bw day(-)(1) for the five age groups, with a mean total daily intake of 0.17 µg kg(-)(1) bw day(-)(1) for the general population. The highest estimated dietary mean daily intake of perchlorate (0.67 µg kg(-)(1) bw day(-)(1)) was found for children at 3-5 years. The estimated dietary perchlorate exposure in Kuwait is higher than the recommended mean reference dose (RfD) but lower than that of provisional maximum tolerable daily intake (PMTDI) set by the Joint FAO/WHO Expert Committee on Food Additives (JECFA). PMID:27248576

  13. Determination of chromium combined with DNA, RNA and proteins in chromium-rich brewer's yeast by NAA

    International Nuclear Information System (INIS)

    The content of chromium in the DNA, RNA and protein fractions separated from chromium-rich and normal brewer's yeast was determined by neutron activation analysis (NAA). Our results show that the extracted relative amounts and concentrations of DNA, RNA and proteins have no significant difference for two types of yeast, but the chromium content in DNA, RNA and proteins fractions extracted from the chromium-rich yeast are substantially higher than those from the normal. In addition, the concentration of chromium in DNA is much higher than that in RNA and proteins. It is evident that the inorganic chromium compounds can enter the yeast cell during the yeast cultivation in the chromium-containing culture medium and are converted into organic chromium species, which are combined with DNA, RNA and proteins. (author)

  14. Chromium allergy and dermatitis: prevalence and main findings

    DEFF Research Database (Denmark)

    Bregnbak, David; Johansen, Jeanne D.; Jellesen, Morten Stendahl;

    2015-01-01

    The history of chromium as an allergen goes back more than a century, and includesan interventional success with national legislation that led to significant changes inthe epidemiology of chromium allergy in construction workers. The 2015 EU Leather Regulation once again put a focus on chromium...

  15. 21 CFR 73.1326 - Chromium hydroxide green.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 1 2010-04-01 2010-04-01 false Chromium hydroxide green. 73.1326 Section 73.1326... COLOR ADDITIVES EXEMPT FROM CERTIFICATION Drugs § 73.1326 Chromium hydroxide green. (a) Identity. (1) The color additive chromium hydroxide green is principally hydrated chromic sesquioxide...

  16. 21 CFR 73.2326 - Chromium hydroxide green.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 1 2010-04-01 2010-04-01 false Chromium hydroxide green. 73.2326 Section 73.2326... COLOR ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2326 Chromium hydroxide green. (a) Identity and specifications.The color additive chromium hydroxide green shall conform in identity and specifications to...

  17. Thermodynamic properties of chromium bearing slags and minerals. A review

    Energy Technology Data Exchange (ETDEWEB)

    Xiao Yanping; Holappa, L.

    1996-12-31

    In this report, the thermodynamic properties of chromium bearing slags and minerals were reviewed based on the available information in the literature. It includes the analysing methods for oxidation state of chromium in slags, oxidation state of chromium and activities of chromium oxides in slags and minerals. The phase diagrams of chromium oxide systems and chromium distributions between slag and metal phases are also covered ill this review. Concerning the analysing methods, it was found that most of the available approaches are limited to iron free slag systems and the sample preparation is very sensitive to the analysing results. In silicate slags under reducing atmosphere, divalent and trivalent chromium co-exist in the slags. It is agreed that the fraction of divalent chromium to total chromium increases with higher temperature, lower slag basicity and oxygen potential. For the slags under oxidising atmosphere, trivalent, pentavalent and hexavalent states were reported to be stable. The activities of CrO and CrO{sub 1.5} were concluded to have positive deviation from ideal solution. Slag basicity has a positive effect and temperature has a negative effect on the activities of chromium oxides. The phase diagrams of the Cr-O, binary, and ternary chromium containing oxide systems have been examined systematically. The analysis shows that the data on the quaternary and quinary systems are insufficient, and require further investigation. The most important features of the chromium containing silicate slags are the large miscibility gaps and the stability of the chromite spinel. (orig.) (76 refs.)

  18. 21 CFR 73.1015 - Chromium-cobalt-aluminum oxide.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 1 2010-04-01 2010-04-01 false Chromium-cobalt-aluminum oxide. 73.1015 Section 73... LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION Drugs § 73.1015 Chromium-cobalt-aluminum oxide. (a) Identity. The color additive chromium-cobalt-aluminum oxide is a blue-green pigment obtained by calcining...

  19. Hexavalent and trivalent chromium in leather: What should be done?

    Science.gov (United States)

    Moretto, Angelo

    2015-11-01

    Trivalent chromium compounds are used for leather tanning, and chromium may be released during use of leather goods. In certain instances, small amounts of hexavalent chromium can be formed and released. Both trivalent and hexavalent chromium can elicit allergic skin reaction in chromium sensitised subjects, the latter being significantly more potent. Induction of sensitisation only occurs after exposure to hexavalent chromium. A minority of subjects are sensitised to chromium, and in a fraction of these subjects allergic skin reaction have been described after wearing leather shoes or, less frequently, other leather goods. The evidence that in all these cases the reaction is related to hexavalent chromium is not always strong. The content of hexavalent chromium in leather is regulated in European Union, but rate of release rather than content is relevant for allergic skin reaction. The role of trivalent chromium appear much less relevant if at all. Modern tanning procedure do not pose significant risk due to either hexavalent or trivalent chromium. Dismissing bad quality and worn-off leather goods is relevant in reducing or eliminating the skin reaction. It should also be pointed out that shoe components or substances other than chromium in leather may cause allergic/irritative skin reactions. PMID:26361854

  20. SAFETY OF TRIVALENT CHROMIUM COMPLEXES USED IN NUTRIENT SUPPLEMENTS

    Science.gov (United States)

    Toxicity studies regarding trivalent chromium have often been completed under conditions that are not designed to reflect conditions that would be encountered under normal physiological conditions. We have shown that the incorporation of chromium into tissues of rats from chromium chloride and chro...

  1. Strategies for chromium bioremediation of tannery effluent.

    Science.gov (United States)

    Garg, Satyendra Kumar; Tripathi, Manikant; Srinath, Thiruneelakantan

    2012-01-01

    Bioremediation offers the possibility of using living organisms (bacteria, fungi, algae,or plants), but primarily microorganisms, to degrade or remove environmental contaminants, and transform them into nontoxic or less-toxic forms. The major advantages of bioremediation over conventional physicochemical and biological treatment methods include low cost, good efficiency, minimization of chemicals, reduced quantity of secondary sludge, regeneration of cell biomass, and the possibility of recover-ing pollutant metals. Leather industries, which extensively employ chromium compounds in the tanning process, discharge spent-chromium-laden effluent into nearby water bodies. Worldwide, chromium is known to be one of the most common inorganic contaminants of groundwater at pollutant hazardous sites. Hexavalent chromium poses a health risk to all forms of life. Bioremediation of chromium extant in tannery waste involves different strategies that include biosorption, bioaccumulation,bioreduction, and immobilization of biomaterial(s). Biosorption is a nondirected physiochemical interaction that occurs between metal species and the cellular components of biological species. It is metabolism-dependent when living biomass is employed, and metabolism-independent in dead cell biomass. Dead cell biomass is much more effective than living cell biomass at biosorping heavy metals, including chromium. Bioaccumulation is a metabolically active process in living organisms that works through adsorption, intracellular accumulation, and bioprecipitation mechanisms. In bioreduction processes, microorganisms alter the oxidation/reduction state of toxic metals through direct or indirect biological and chemical process(es).Bioreduction of Cr6+ to Cr3+ not only decreases the chromium toxicity to living organisms, but also helps precipitate chromium at a neutral pH for further physical removal,thus offering promise as a bioremediation strategy. However, biosorption, bioaccumulation, and

  2. Collisional properties of trapped cold chromium atoms

    CERN Document Server

    Pavlovich, Z; Côté, R; Sadeghpour, H R; Pavlovic, Zoran; Roos, Bjoern O.; Côté, Robin

    2004-01-01

    We report on calculations of the elastic cross section and thermalization rate for collision between two maximally spin-polarized chromium atoms in the cold and ultracold regimes, relevant to buffer-gas and magneto-optical cooling of chromium atoms. We calculate ab initio potential energy curves for Cr2 and the van der Waals coefficient C6, and construct interaction potentials between two colliding Cr atoms. We explore the effect of shape resonances on elastic cross section, and find that they dramatically affect the thermalization rate. Our calculated value for the s-wave scattering length is compared in magnitude with a recent measurement at ultracold temperatures.

  3. Influence of nitrogen on the structure and properties of chromium, chromium-molybdenum and chromium-manganese steels

    International Nuclear Information System (INIS)

    Phase transformations, precipitation processes and properties of the chromium, chromium-molybdenum and chromium-manganese steels with a high content of nitrogen as the dependence on thermal treatment were investigated. In case of Fe-0.08C-18Cr-18Mn-N and Fe-0.08C-18Cr-18Mn-2Mo-N steels the samples in the state after solution at temperature 1050oC and 1150oC and 1250oC and after subsequent annealing in 600oC and 800oC were investigated. heat treatment of the Fe-0.5C-10Cr-N and Fe-0.5C-10Cr-1Mo-N steels included austenitizment from 1000oC with air cooling and hardening from 1000oC with oil cooling and tempering in 650oC and 750oC in two hours with cooling in the air. These investigations show that the influence of nitrogen as an alloy element on the phase transformations, precipitation processes, mechanical and corrosion properties is connected with the presence of molybdenum and chromium in the steel. Nitrogen with these elements creates complex ions with the coordinate number 6. This statement is formed on the base of both calculations and investigation results. (author)

  4. Inhibition of microbial sulfate reduction in a flow-through column system by (per)chlorate treatment.

    Science.gov (United States)

    Engelbrektson, Anna; Hubbard, Christopher G; Tom, Lauren M; Boussina, Aaron; Jin, Yong T; Wong, Hayden; Piceno, Yvette M; Carlson, Hans K; Conrad, Mark E; Anderson, Gary; Coates, John D

    2014-01-01

    Microbial sulfate reduction is a primary cause of oil reservoir souring. Here we show that amendment with chlorate or perchlorate [collectively (per)chlorate] potentially resolves this issue. Triplicate packed columns inoculated with marine sediment were flushed with coastal water amended with yeast extract and one of nitrate, chlorate, or perchlorate. Results showed that although sulfide production was dramatically reduced by all treatments, effluent sulfide was observed in the nitrate (10 mM) treatment after an initial inhibition period. In contrast, no effluent sulfide was observed with (per)chlorate (10 mM). Microbial community analyses indicated temporal community shifts and phylogenetic clustering by treatment. Nitrate addition stimulated Xanthomonadaceae and Rhizobiaceae growth, supporting their role in nitrate metabolism. (Per)chlorate showed distinct effects on microbial community structure compared with nitrate and resulted in a general suppression of the community relative to the untreated control combined with a significant decrease in sulfate reducing species abundance indicating specific toxicity. Furthermore, chlorate stimulated Pseudomonadaceae and Pseudoalteromonadaceae, members of which are known chlorate respirers, suggesting that chlorate may also control sulfidogenesis by biocompetitive exclusion of sulfate-reduction. Perchlorate addition stimulated Desulfobulbaceae and Desulfomonadaceae, which contain sulfide oxidizing and elemental sulfur-reducing species respectively, suggesting that effluent sulfide concentrations may be controlled through sulfur redox cycling in addition to toxicity and biocompetitive exclusion. Sulfur isotope analyses further support sulfur cycling in the columns, even when sulfide is not detected. This study indicates that (per)chlorate show great promise as inhibitors of sulfidogenesis in natural communities and provides insight into which organisms and respiratory processes are involved. PMID:25071731

  5. Electrodeposition of black chromium thin films from trivalent chromium-ionic liquid solution

    OpenAIRE

    Eugénio, S.; Vilar, Rui; C. M. Rangel; Baskaran, I.

    2009-01-01

    In the present study, black chromium thin films were electrodeposited from a solution of 1-butyl-3- methylimidazolium tetrafluoroborate ([BMIm][BF4] ionic liquid containing trivalent chromium (Cr(III)). Homogeneous and well adherent coatings have been obtained on nickel, copper and stainless steel substrates. The nucleation and growth of the films were investigated by cyclic voltammetry and current-density/time transient techniques. SEM/EDS, XPS and XRD were used to study the morphology, chem...

  6. Reduction of Hexavalent Chromium by Viable Cells of Chromium Resistant Bacteria Isolated from Chromite Mining Environment

    OpenAIRE

    Satarupa Dey; Baishali Pandit; A. K. Paul

    2014-01-01

    Environmental contamination of hexavalent chromium [Cr(VI)] is of serious concern for its toxicity as well as mutagenic and carcinogenic effects. Bacterial chromate reduction is a cost-effective technology for detoxification as well as removal of Cr(VI) from polluted environment. Chromium resistant and reducing bacteria, belonging to Arthrobacter, Pseudomonas, and Corynebacterium isolated from chromite mine overburden and seepage samples of Orissa, India, were found to tolerate 12–18 mM Cr(VI...

  7. Reduction of Chromium-VI by Chromium Resistant Lactobacilli: A Prospective Bacterium for Bioremediation

    OpenAIRE

    Mishra, Ritesh; Sinha, Vartika; Kannan, Ambrose; Upreti, Raj K.

    2012-01-01

    Chromium is a toxic heavy metal, which primarily exists in two inorganic forms, Cr (VI) and Cr (III). Highly soluble hexavalent chromium is carcinogenic due to its oxidizing nature. It is well established that the intestinal bacteria including Lactobacilli have regulatory effect on intestinal homeostasis and a breakdown in the relationship between intestinal cells and bacteria results in the manifestation of gastrointestinal (GI) disorders. In this study Cr (VI) resistance was developed in La...

  8. Mechanical properties of metal-ceramic systems from nickel-chromium and cobalt-chromium alloys

    OpenAIRE

    Mirković Nemanja

    2007-01-01

    Background/Aim. Metal-ceramic bond strength and alloys' elastic modulus clearly determine the potential of alloy application, because the ceramic integrity during mastication depends on these two characteristics. The aim of this study was to evaluate metal-ceramic bond strength and elastic modulus of cobalt-chromium alloys in making porcelainfused- to-metal restorations, regarding the application of the most frequent nickel-chromium alloy. Methods. The research was performed as an experimenta...

  9. Rapid measurement of perchlorate in polar ice cores down to sub-ng L(-1) levels without pre-concentration.

    Science.gov (United States)

    Peterson, Kari; Cole-Dai, Jihong; Brandis, Derek; Cox, Thomas; Splett, Scott

    2015-10-01

    An ion chromatography-electrospray ionization-tandem mass spectrometry (IC-ESI-MS/MS) method has been developed for rapid and accurate measurement of perchlorate in polar snow and ice core samples in which perchlorate concentrations are expected to be as low as 0.1 ng L(-1). Separation of perchlorate from major inorganic species in snow is achieved with an ion chromatography system interfaced to an AB SCIEX triple quadrupole mass spectrometer operating in multiple reaction monitoring mode. Under optimized conditions, the limit of detection and lower limit of quantification without pre-concentration have been determined to be 0.1 and 0.3 ng L(-1), respectively, with a linear dynamic range of 0.3-10.0 ng L(-1) in routine measurement. These represent improvements over previously reported methods using similar analytical techniques. The improved method allows fast, accurate, and reproducible perchlorate quantification down to the sub-ng L(-1) level and will facilitate perchlorate measurement in the study of natural perchlorate production with polar ice cores in which perchlorate concentrations are anticipated to vary in the low and sub-ng L(-1) range. Initial measurements of perchlorate in ice core samples from central Greenland show that typical perchlorate concentrations in snow dated prior to the Industrial Revolution are about 0.8 ng L(-1), while perchlorate concentrations are significantly higher in recent (post-1980) snow, suggesting that anthropogenic sources are a significant contributor to perchlorate in the current environment. PMID:26297465

  10. Chromium-manganese steels of transition class

    International Nuclear Information System (INIS)

    Possibilities of nickel replacing by manganese and preparing the same level of mechanical properties as in chromium-nickel steels due to γ-α transformations taking place during property tests, are studied. Chromium-manganese steels with the composition of 0.05-0.1%C, 13-14%Cr, 5.0-6.5%Mn, 0.2-0.5%Si, 0.03-0.13%N, 0.05-0.01%Al and additionally alloyed 0.3-2.0%Cu, 0.05-0.6%V, 0.3-1.0%Mo, 0.02-0.05%Ca in various combinations have been melted. It is shown, that using alloying and heat treatment one can control the phase composition, austenite resistance to martensite transformation during loading and mechanical properties of chromium-manganese steels of the transition class. The use of the phase transformation in the process of testing determines the level of mechanical properties. The optimum development of the transformation accompanied by a sufficient development of processes of hardening and microstresses relaxation permits to obtain a high level of mechanical properties: σsub(B)=1500 MPa, σsub(0.2)-1130MPa, delta=15%, psi=37%, asub(H)=1000 kJ/msup(2) which exceeds the level for chromium-nickel steels. Steels have a lower cost and do not require any complecated heat treatment regime

  11. Defect structure of electrodeposited chromium layers

    International Nuclear Information System (INIS)

    Positron annihilation spectroscopy was applied to study the effects of pre-treatment and composition of substrates on the quality and defect structure of electrodeposited thick chromium coatings. The results show that both parameters are important, and a scenario is proposed why the mechanically polished substrate gives more defective film than the electro polished one.

  12. Defect structure of electrodeposited chromium layers

    CERN Document Server

    Marek, T; Vertes, A; El-Sharif, M; McDougall, J; Chisolm, C U

    2000-01-01

    Positron annihilation spectroscopy was applied to study the effects of pre-treatment and composition of substrates on the quality and defect structure of electrodeposited thick chromium coatings. The results show that both parameters are important, and a scenario is proposed why the mechanically polished substrate gives more defective film than the electro polished one.

  13. Flashlamp-pumped lasing of chromium: GSGG

    International Nuclear Information System (INIS)

    Lasing action in chromium-doped gadolinium scandium gallium garnet (Cr:GSGG) is well established for both CW/sup (1)/ and flashlamp/sup (2)/ pumping. This paper describes an investigation of flashlamp-pumped Cr:GSGG lasers and indicates some of the factors which limit performance

  14. Trace Elements Excluding Iron - Chromium and Zinc

    Science.gov (United States)

    The percentage of middle-aged US adults who are participating in leisure-time physical activities is growing. These adults also seek credible information about specific supplements that the public press routinely describes as necessary to enable increases in physical performance. Chromium and zinc a...

  15. HEALTH ASSESSMENT DOCUMENT FOR CHROMIUM. FINAL REPORT

    Science.gov (United States)

    The full document represents a comprehensive data base that considers all sources of chromium in the environment, the likelihood for its exposure to humans, and the possible consequences to man and lower organisms from its absorption. This information is integrated into a format ...

  16. 29 CFR 1926.1126 - Chromium (VI).

    Science.gov (United States)

    2010-07-01

    ... CFR 1926.51 Where skin contact with chromium (VI) occurs, the employer shall provide washing facilities in conformance with 29 CFR 1926.51. Eating and drinking areas provided by the employer shall also... requirements of the Hazard Communication Standard, 29 CFR 1910.1200. (3) Cleaning and replacement. (i)...

  17. 29 CFR 1910.1026 - Chromium (VI).

    Science.gov (United States)

    2010-07-01

    ... CFR 1910.141. Where skin contact with chromium (VI) occurs, the employer shall provide washing facilities in conformance with 29 CFR 1910.141. Eating and drinking areas provided by the employer shall also... requirements of the Hazard Communication Standard, 29 CFR 1910.1200. (3) Cleaning and replacement. (i)...

  18. 29 CFR 1915.1026 - Chromium (VI).

    Science.gov (United States)

    2010-07-01

    ... CFR 1910.141. Where skin contact with chromium (VI) occurs, the employer shall provide washing facilities in conformance with 29 CFR 1915.97. Eating and drinking areas provided by the employer shall also... requirements of the Hazard Communication Standard, 29 CFR 1910.1200. (3) Cleaning and replacement. (i)...

  19. Chromium(III) and chromium(VI) surface treated galvanized steel for outdoor constructions: environmental aspects.

    Science.gov (United States)

    Lindström, David; Hedberg, Yolanda; Odnevall Wallinder, Inger

    2010-06-01

    The long-term degradation of chromium(III) (Zn-Cr(III)) and chromium(VI)-based (Zn-Cr(VI)) surface treatments on galvanized steel and their capacities to hinder the release of zinc induced by atmospheric corrosion at nonsheltered urban and marine exposure conditions for 2 years are investigated. Compared to bare zinc sheet, both surface treatments revealed high corrosion protection abilities and capacities to hinder the release of zinc, still evident after 2 years of exposure. The zinc barrier properties of the thinner Zn-Cr(VI) (10 nm) treatment were during the first 100 days of urban exposure slightly improved compared with Zn-Cr(III) (35 nm). However, their long-term protection capacities were inverse. Released concentrations of total chromium correspond to annual release rates less than 0.000032 (Zn-Cr(III)) and 0.00014 g Cr m(-2) yr(-1) (Zn-Cr(VI)) after 1 year of urban exposure. Aging by indoor storage of the surface treatments prior to outdoor exposure reduced the released Cr concentrations from the surface treatments. No Cr(VI) was released from the aged surfaces but from the freshly exposed Zn-Cr(VI). Marine exposure conditions resulted in a faster reduction of chromate to chromium(III)oxide compared with urban conditions, and a significantly lower amount of both chromium(III) and chromium(VI) released from Zn-Cr(VI) at the marine site compared with the urban site. PMID:20462267

  20. Biological groundwater treatment for chromium removal at low hexavalent chromium concentrations.

    Science.gov (United States)

    Mamais, Daniel; Noutsopoulos, Constantinos; Kavallari, Ioanna; Nyktari, Eleni; Kaldis, Apostolos; Panousi, Eleni; Nikitopoulos, George; Antoniou, Kornilia; Nasioka, Maria

    2016-06-01

    The objective of this work is to develop and evaluate biological groundwater treatment systems that will achieve hexavalent chromium reduction and total chromium removal from groundwater at hexavalent chromium (Cr(VI)) groundwater concentrations in the 0-200 μg/L range. Three lab-scale units operated, as sequencing batch reactors (SBR) under aerobic, anaerobic and anaerobic-aerobic conditions. All systems received groundwater with a Cr(VI) content of 200 μg/L. In order to support biological growth, groundwater was supplemented with milk, liquid cheese whey or a mixture of sugar and milk to achieve a COD concentration of 200 mg/L. The results demonstrate that a fully anaerobic system or an anaerobic-aerobic system dosed with simple or complex external organic carbon sources can lead to practically complete Cr(VI) reduction to Cr(III). The temperature dependency of maximum Cr(VI) removal rates can be described by the Arrhenius relationship. Total chromium removal in the biological treatment systems was not complete because a significant portion of Cr(III) remained in solution. An integrated system comprising of an anaerobic SBR followed by a sand filter achieved more than 95% total chromium removal thus resulting in average effluent total and dissolved chromium concentrations of 7 μg/L and 3 μg/L, respectively. PMID:26971177

  1. Nephrotoxic and hepatotoxic effects of chromium compounds in rats

    Energy Technology Data Exchange (ETDEWEB)

    Laborda, R.; Diaz-Mayans, J.; Nunez, A.

    1986-03-01

    The nephrotoxic, hepatotoxic and cardiotoxic actions of hexavalent chromium compounds, as well as their effects on lung, blood and circulation may contribute to the fatal outcome of chromium intoxication. Although trivalent chromium have been regarded as relatively biologically inert, there are a few salts of chromium III that have been found to be carcinogenic when inhaled, ingested or brought in contact with the tissues. Sensitive persons and industry workers have been subjects of dermatitis, respiratory tract injuries and digestive ulcers due to chromium compounds. In this work, the authors have studied the effect of trivalent and hexavalent chromium compounds on rats measuring the transaminases (GOT and GPT), urea and creatinine levels in serum of chromium poisoned animals at different times.

  2. A Kinetic Model of Chromium in a Flame

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Chromium has been identified as a carcinogenic metal.Incineration is the useful method for disposal of toxic chromium hazard waste and a chromium kinetic model in a flame is very important to study chromium oxidation.Chromium chemical kinetics over a range of temperatures of a hydrogen/air flame is proposed.Nine chromium compounds and fifty-eight reversible chemical reactions were considered The forward reaction rates are calculated based on the molecular collision approach for unknown ones and Arrhenius's Law for known ones.The backward reaction rates were calculated according to forward reaction rates, the equilibrium constants and chemical thermodynamics.It is verified by several equilibrium cases and is tested by a hydrogen/air diffusion flame.The results show that the kinetic model could be used in cases in which the chromium kinetics play an important role in a flame

  3. The Chromium is an essential element in the human

    International Nuclear Information System (INIS)

    The Chromium is an essential element for human and animals, because it a preponderant function in the insulin metabolism as a glucose tolerance factor (GTF). The deficiency of chromium engenders a deterioration in the glucose metabolism due to bad efficiency of insulin. Because the importance of this element an exhaustive reference review was made and this presents some studies realized in laboratory animals and in human beings where it is prove with resuits the effect of chromium over the improvement of patients with non-insulin dependant diabetes. Three substances are presented as chromium active biological forms: a material rich in chromium known as glucose tolerance factor, chromium picolinate and a substance of low molecular weight LMWCr in its forms of apo and holo that contains chromium and it links the insulin receptor and improves its activity. Also this paper presents information about the condition of diabetes in Costa Rica. (Author)

  4. Reaction of chromium(VI) with glutathione or with hydrogen peroxide: identification of reactive intermediates and their role in chromium(VI)-induced DNA damage.

    OpenAIRE

    Aiyar, J; Berkovits, H J; Floyd, R A; Wetterhahn, K E

    1991-01-01

    The types of reactive intermediates generated upon reduction of chromium(VI) by glutathione or hydrogen peroxide and the resulting DNA damage have been determined. In vitro, reaction of chromium(VI) with glutathione led to formation of two chromium(V) complexes and the glutathione thiyl radical. When chromium(VI) was reacted with DNA in the presence of glutathione, chromium-DNA adducts were obtained, with no DNA strand breakage. The level of chromium-DNA adduct formation correlated with chrom...

  5. (Per)chlorate reduction by the thermophilic bacterium Moorella perchloratireducens sp. nov., isolated from underground gas storage.

    Science.gov (United States)

    Balk, Melike; van Gelder, Ton; Weelink, Sander A; Stams, Alfons J M

    2008-01-01

    A thermophilic bacterium, strain An10, was isolated from underground gas storage with methanol as a substrate and perchlorate as an electron acceptor. Cells were gram-positive straight rods, 0.4 to 0.6 mum in diameter and 2 to 8 mum in length, growing as single cells or in pairs. Spores were terminal with a bulged sporangium. The temperature range for growth was 40 to 70 degrees C, with an optimum at 55 to 60 degrees C. The pH optimum was around 7. The salinity range for growth was between 0 and 40 g NaCl liter(-1) with an optimum at 10 g liter(-1). Strain An10 was able to grow on CO, methanol, pyruvate, glucose, fructose, cellobiose, mannose, xylose, and pectin. The isolate was able to respire with (per)chlorate, nitrate, thiosulfate, neutralized Fe(III) complexes, and anthraquinone-2,6-disulfonate. The G+C content of the DNA was 57.6 mol%. On the basis of 16S rRNA analysis, strain An10 was most closely related to Moorella thermoacetica and Moorella thermoautotrophica. The bacterium reduced perchlorate and chlorate completely to chloride. Key enzymes, perchlorate reductase and chlorite dismutase, were detected in cell extracts. Strain An10 is the first thermophilic and gram-positive bacterium with the ability to use (per)chlorate as a terminal electron acceptor. PMID:17981952

  6. Design and performance of chromium mist generator

    Directory of Open Access Journals (Sweden)

    Tirgar Aram

    2006-01-01

    Full Text Available Chromium mist generator is an essential tool for conducting researches and making science-based recommendations to evaluate air pollution and its control systems. The purpose of this research was to design and construct a homogenous chromium mist generator and the study of some effective factors including sampling height and distances between samplers in side-by-side sampling on chromium mist sampling method. A mist generator was constructed, using a chromium electroplating bath in pilot scale. Concentration of CrO3 and sulfuric acid in plating solution was 125 g L-1 and 1.25 g L-1, respectively. In order to create permanent air sampling locations, a Plexiglas cylindrical chamber (75 cm height, 55 cm i.d was installed the bath overhead. Sixty holes were produced on the chamber in 3 rows (each 20. The distance between rows and holes was 15 and 7.5 cm, respectively. Homogeneity and effective factors were studied via side-by-side air sampling method. So, 48 clusters of samples were collected on polyvinyl chloride (PVC filters housed in sampling cassettes. Cassettes were located in 35, 50, and 65 cm above the solution surface with less than 7.5 and/or 7.5-15 cm distance between heads. All samples were analyzed according to the NIOSH method 7600. According to the ANOVA test, no significant differences were observed between different sampling locations in side-by-side sampling (P=0.82 and between sampling heights and different samplers distances (P=0.86 and 0.86, respectively. However, there were notable differences between means of coefficient of variations (CV in various heights and distances. It is concluded that the most chromium mist homogeneity could be obtained at height 50 cm from the bath solution surface and samplers distance of < 7.5 cm.

  7. Light and variable 37Cl/35Cl ratios in rocks from Gale Crater, Mars: Possible signature of perchlorate

    Science.gov (United States)

    Farley, K. A.; Martin, P.; Archer, P. D.; Atreya, S. K.; Conrad, P. G.; Eigenbrode, J. L.; Fairén, A. G.; Franz, H. B.; Freissinet, C.; Glavin, D. P.; Mahaffy, P. R.; Malespin, C.; Ming, D. W.; Navarro-Gonzalez, R.; Sutter, B.

    2016-03-01

    Cl isotope ratios measured on HCl thermally evolved from as-yet-unknown phases in sedimentary rocks and sand in Gale Crater provide unexpected insights to the Martian surficial Cl cycle. The seven samples yield δ37Cl values ranging from - 1 ± 25 ‰ to - 51 ± 5 ‰. Five analyses from two samples of the Sheepbed mudstone (Yellowknife Bay study area) are analytically indistinguishable with a mean δ37Cl of - 11 ± 7 ‰ (1 σ). In contrast, four mudstones/sandstones from the Kimberley and Pahrump study areas also yielded indistinguishable ratios, but with a mean δ37Cl of - 43 ± 6 ‰. The Rocknest sand deposit gave a highly uncertain δ37Cl value of - 7 ± 44 ‰. These light and highly variable δ37Cl values are unique among known solar system materials. Two endmember models are offered to account for these observations, and in both, perchlorate, with its extreme ability to fractionate Cl isotopes, is critical. In the first model, SAM is detecting HCl from an oxychlorine compound (e.g., perchlorate) produced from volcanic gas emissions by atmospheric chemical reactions. Similar reactions in Earth's atmosphere may be responsible for the isotopically lightest known Cl outside of this study, in perchlorate from the Atacama Desert. Some of the Gale Crater δ37Cl values are more negative than those in Atacama perchlorate, but because reaction mechanisms and associated fractionation factors are unknown, it is impossible to assess whether this difference is prohibitive. If the negative δ37Cl signal is produced in this fashion, the isotopic variability among samples could arise either from variations in the relative size of the reactant chloride and product perchlorate reservoirs, or from variations in the fraction of perchlorate reduced back to chloride after deposition. Such reduction strongly enriches 37Cl in the residual perchlorate. Perchlorate reduction alone offers an alternative endmember model that can explain the observed data if SAM measured HCl derived

  8. Electron donors and co-contaminants affect microbial community composition and activity in perchlorate degradation.

    Science.gov (United States)

    Guan, Xiangyu; Xie, Yuxuan; Wang, Jinfeng; Wang, Jing; Liu, Fei

    2015-04-01

    Although microbial reduction of perchlorate (ClO4(-)) is a promising and effective method, our knowledge on the changes in microbial communities during ClO4(-) degradation is limited, especially when different electron donors are supplied and/or other contaminants are present. Here, we examined the effects of acetate and hydrogen as electron donors and nitrate and ammonium as co-contaminants on ClO4(-) degradation by anaerobic microcosms using six treatments. The process of degradation was divided into the lag stage (SI) and the accelerated stage (SII). Quantitative PCR was used to quantify four genes: pcrA (encoding perchlorate reductase), cld (encoding chlorite dismutase), nirS (encoding copper and cytochrome cd1 nitrite reductase), and 16S rRNA. While the degradation of ClO4(-) with acetate, nitrate, and ammonia system (PNA) was the fastest with the highest abundance of the four genes, it was the slowest in the autotrophic system (HYP). The pcrA gene accumulated in SI and played a key role in initiating the accelerated degradation of ClO4(-) when its abundance reached a peak. Degradation in SII was primarily maintained by the cld gene. Acetate inhibited the growth of perchlorate-reducing bacteria (PRB), but its effect was weakened by nitrate (NO3(-)), which promoted the growth of PRB in SI, and therefore, accelerated the ClO4(-) degradation rate. In addition, ammonia (NH4(+)), as nitrogen sources, accelerated the growth of PRB. The bacterial communities' structure and diversity were significantly affected by electron donors and co-contaminants. Under heterotrophic conditions, both ammonia and nitrate promoted Azospira as the most dominant genera, a fact that might significantly influence the rate of ClO4(-) natural attenuation by degradation. PMID:25382499

  9. The Effects of Perchlorates on the Permafrost Methanogens: Implication for Autotrophic Life on Mars

    Directory of Open Access Journals (Sweden)

    Viktoria Shcherbakova

    2015-09-01

    Full Text Available The terrestrial permafrost represents a range of possible cryogenic extraterrestrial ecosystems on Earth-like planets without obvious surface ice, such as Mars. The autotrophic and chemolithotrophic psychrotolerant methanogens are more likely than aerobes to function as a model for life forms that may exist in frozen subsurface environments on Mars, which has no free oxygen, inaccessible organic matter, and extremely low amounts of unfrozen water. Our research on the genesis of methane, its content and distribution in permafrost horizons of different ages and origin demonstrated the presence of methane in permanently frozen fine-grained sediments. Earlier, we isolated and described four strains of methanogenic archaea of Methanobacterium and Methanosarcina genera from samples of Pliocene and Holocene permafrost from Eastern Siberia. In this paper we study the effect of sodium and magnesium perchlorates on growth of permafrost and nonpermafrost methanogens, and present evidence that permafrost hydogenotrophic methanogens are more resistant to the chaotropic agent found in Martian soil. In this paper we study the effect of sodium and magnesium perchlorates on the growth of permafrost and nonpermafrost methanogens, and present evidence that permafrost hydogenotrophic methanogens are more resistant to the chaotropic agent found in Martian soil. Furthermore, as shown in the studies strain M2T M. arcticum, probably can use perchlorate anion as an electron acceptor in anaerobic methane oxidation. Earth’s subzero subsurface environments are the best approximation of environments on Mars, which is most likely to harbor methanogens; thus, a biochemical understanding of these pathways is expected to provide a basis for designing experiments to detect autotrophic methane-producing life forms on Mars.

  10. Chromium supplementation improved post-stroke brain infarction and hyperglycemia.

    Science.gov (United States)

    Chen, Wen-Ying; Mao, Frank Chiahung; Liu, Chia-Hsin; Kuan, Yu-Hsiang; Lai, Nai-Wei; Wu, Chih-Cheng; Chen, Chun-Jung

    2016-04-01

    Hyperglycemia is common after acute stroke and is associated with a worse outcome of stroke. Thus, a better understanding of stress hyperglycemia is helpful to the prevention and therapeutic treatment of stroke. Chromium is an essential nutrient required for optimal insulin activity and normal carbohydrate and lipid metabolism. Beyond its nutritional effects, dietary supplement of chromium causes beneficial outcomes against several diseases, in particular diabetes-associated complications. In this study, we investigated whether post-stroke hyperglycemia involved chromium dynamic mobilization in a rat model of permanent focal cerebral ischemia and whether dietary supplement of chromium improved post-stroke injury and alterations. Stroke rats developed brain infarction, hyperglycemia, hyperinsulinemia, glucose intolerance, and insulin resistance. Post-stroke hyperglycemia was accompanied by elevated secretion of counter-regulatory hormones including glucagon, corticosterone, and norepinephrine, decreased insulin signaling in skeletal muscles, and increased hepatic gluconeogenesis. Correlation studies revealed that counter-regulatory hormone secretion showed a positive correlation with chromium loss and blood glucose increased together with chromium loss. Daily chromium supplementation increased tissue chromium levels, attenuated brain infarction, improved hyperglycemia, and decreased plasma levels of glucagon and corticosterone in stroke rats. Our findings suggest that stroke rats show disturbance of tissue chromium homeostasis with a net loss through urinary excretion and chromium mobilization and loss might be an alternative mechanism responsible for post-stroke hyperglycemia. PMID:26477944

  11. Development of Biosensors for Real Time Analysis of Perchlorate in Water

    OpenAIRE

    Frankenberger, William T.; Okeke, Benedict C.; Cheng, Quan Jason

    2006-01-01

    Perchlorate (ClO4 -) contamination of ground water is a widespread problem in the U.S., which can adversely affect human health and wildlife. Current methods for detecting and quantifying ClO4 - in water are time consuming, expensive, and subject to error due to complex procedures and various interferences. Thus, there is an urgent need to develop a method that can accurately detect and measure low concentrations of ClO4 - in the field. This study reports the construction of a ClO4 -- reducta...

  12. Bis(1,10-phenanthroline)lithium perchlorate: crystal structure and dissociation of complex in acetone

    International Nuclear Information System (INIS)

    Composition of solid phase formed in acetone at concentration ratios of 1,10-phenanthroline (phen) and LiClO4 near 2:1 is established. Molecular structure of bis(1,10-phenanthroline)lithium perchlorate is determined by X-ray structural analysis: space group Pnna, a=7.191(2), b=39.929(9), c=14.494(3) A, Z=8, Dx=1.490 g/cm3. Data of IR spectroscopy in acetone denotes dissociation of the Li(phen)2ClO4 complex for the 1:1 composition complex and molecule phen in the solution equilibrium with the solid phase

  13. Lanthanide perchlorate complexes of quinoline-1-oxide and isoquinoline-2-oxide

    OpenAIRE

    Kalyanasundaram, R; Navaneetham, NS; Soundararajan, S.

    1985-01-01

    Complexes of lanthanide perchlorates with quinoline-1-oxide and isoquinoline-2-oxide have been isolated for the first time characterised by analysis, conductance and IR, NMR and electronic spectoral studies. The complexes of quinoline-1-oxide have the composition $Ln(QNO)_8$$(ClO_4)_3$ where Ln = La, Pr or Nd and $Ln(QNO)_7$ where Ln = Gd, Dy, Ho, Er, Yb. The isoquinoline-2-oxide complexes analyse for the formula $Ln(IsoQNO)_7(ClO_4)_3$ where Ln = La-Yb.

  14. (Per)chlorate reduction by an acetogenic bacterium, Sporomusa sp., isolated from an underground gas storage

    OpenAIRE

    2010-01-01

    A mesophilic bacterium, strain An4, was isolated from an underground gas storage reservoir with methanol as substrate and perchlorate as electron acceptor. Cells were Gram-negative, spore-forming, straight to curved rods, 0.5–0.8 μm in diameter, and 2–8 μm in length, growing as single cells or in pairs. The cells grew optimally at 37°C, and the pH optimum was around 7. Strain An4 converted various alcohols, organic acids, fructose, acetoin, and H2/CO2 to acetate, usually as the only product. ...

  15. (Per)chlorate reduction by an acetogenic bacterium, Sporomusa sp., isolated from an underground gas storage

    OpenAIRE

    Balk, M.; Mehboob, F.; Gelder, van, M.; Rijpstra, I.; Sinninghe-Damsté, J.S.; Stams, A.J.M.

    2010-01-01

    A mesophilic bacterium, strain An4, was isolated from an underground gas storage reservoir with methanol as substrate and perchlorate as electron acceptor. Cells were Gram-negative, spore-forming, straight to curved rods, 0.5-0.8 microm in diameter, and 2-8 microm in length, growing as single cells or in pairs. The cells grew optimally at 37 degrees C, and the pH optimum was around 7. Strain An4 converted various alcohols, organic acids, fructose, acetoin, and H(2)/CO(2) to acetate, usually a...

  16. (Per)chlorate reduction by an acetogenic bacterium, Sporomusa sp., isolated from an underground gas storage

    OpenAIRE

    Balk, M.; Mehboob, F.; van Gelder, T; Rijpstra, W.I.C.; J. S. Sinninghe Damsté; Stams, A.J.M.

    2010-01-01

    A mesophilic bacterium, strain An4, was isolated from an underground gas storage reservoir with methanol as substrate and perchlorate as electron acceptor. Cells were Gram-negative, spore-forming, straight to curved rods, 0.5–0.8 μm in diameter, and 2–8 μm in length, growing as single cells or in pairs. The cells grew optimally at 37°C, and the pH optimum was around 7. Strain An4 converted various alcohols, organic acids, fructose, acetoin, and H2/CO2 to acetate, usually as the only product. ...

  17. 2-(2-Hydroxy-3-methoxyphenyl-1H-benzimidazol-3-ium perchlorate

    Directory of Open Access Journals (Sweden)

    Chuan Chen

    2012-06-01

    Full Text Available In the title molecular salt, C14H13N2O2+·ClO4−, the ring systems in the cation are almost coplanar [dihedral angle = 5.53 (13°]. Intramolecular N—H...O and O—H...O hydrogen bonds generate S(6 and S(5 rings, respectively. In the crystal, the two H atoms involved in the intramolecular hydrogen bonds also participate in intermolecular links to acceptor O atoms of the perchlorate anions. A simple intermolecular N—H...O bond also occurs. Together, these form a double-chain structure along [101].

  18. Combined effects of perchlorate, thiocyanate, and iodine on thyroid function in the National Health and Nutrition Examination Survey 2007–08

    Energy Technology Data Exchange (ETDEWEB)

    Steinmaus, Craig, E-mail: craigs@berkeley.edu [Office of Environmental Health Hazard Assessment, California Environmental Protection Agency, 1515 Clay St. 16th Floor, Oakland, CA 94612 (United States); Miller, Mark D., E-mail: ucsfpehsumiller@gmail.com [Office of Environmental Health Hazard Assessment, California Environmental Protection Agency, 1515 Clay St. 16th Floor, Oakland, CA 94612 (United States); Cushing, Lara, E-mail: lara.cushing@berkeley.edu [Energy and Resources Group, 310 Barrows Hall, University of California, Berkeley, CA 93720-3050 (United States); Blount, Benjamin C., E-mail: bkb3@cdc.gov [Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, 4770 Buford Highway, NE, Mail Stop F47, Atlanta, GA (United States); Smith, Allan H., E-mail: ahsmith@berkeley.edu [Arsenic Health Effects Research Group, 1950 Addison St., Suite 204, University of California, Berkeley, CA 94704 (United States)

    2013-05-15

    Perchlorate, thiocyanate, and low iodine intake can all decrease iodide intake into the thyroid gland. This can reduce thyroid hormone production since iodide is a key component of thyroid hormone. Previous research has suggested that each of these factors alone may decrease thyroid hormone levels, but effect sizes are small. We hypothesized that people who have all three factors at the same time have substantially lower thyroid hormone levels than people who do not, and the effect of this combined exposure is substantially larger than the effects seen in analyses focused on only one factor at a time. Using data from the 2007–2008 National Health and Nutrition Examination Survey, subjects were categorized into exposure groups based on their urinary perchlorate, iodine, and thiocyanate concentrations, and mean serum thyroxine concentrations were compared between groups. Subjects with high perchlorate (n=1939) had thyroxine concentrations that were 5.0% lower (mean difference=0.40 μg/dl, 95% confidence interval=0.14–0.65) than subjects with low perchlorate (n=2084). The individual effects of iodine and thiocyanate were even smaller. Subjects with high perchlorate, high thiocyanate, and low iodine combined (n=62) had thyroxine concentrations 12.9% lower (mean difference=1.07 μg/dl, 95% confidence interval=0.55–1.59) than subjects with low perchlorate, low thiocyanate, and adequate iodine (n=376). Potential confounders had little impact on results. Overall, these results suggest that concomitant exposure to perchlorate, thiocyanate, and low iodine markedly reduces thyroxine production. This highlights the potential importance of examining the combined effects of multiple agents when evaluating the toxicity of thyroid-disrupting agents. -- Highlights: ► Recent data suggest that essentially everyone in the US is exposed to perchlorate. ► Perchlorate exposure may be associated with lower thyroid hormone levels. ► Some groups may be more susceptible to

  19. Combined effects of perchlorate, thiocyanate, and iodine on thyroid function in the National Health and Nutrition Examination Survey 2007–08

    International Nuclear Information System (INIS)

    Perchlorate, thiocyanate, and low iodine intake can all decrease iodide intake into the thyroid gland. This can reduce thyroid hormone production since iodide is a key component of thyroid hormone. Previous research has suggested that each of these factors alone may decrease thyroid hormone levels, but effect sizes are small. We hypothesized that people who have all three factors at the same time have substantially lower thyroid hormone levels than people who do not, and the effect of this combined exposure is substantially larger than the effects seen in analyses focused on only one factor at a time. Using data from the 2007–2008 National Health and Nutrition Examination Survey, subjects were categorized into exposure groups based on their urinary perchlorate, iodine, and thiocyanate concentrations, and mean serum thyroxine concentrations were compared between groups. Subjects with high perchlorate (n=1939) had thyroxine concentrations that were 5.0% lower (mean difference=0.40 μg/dl, 95% confidence interval=0.14–0.65) than subjects with low perchlorate (n=2084). The individual effects of iodine and thiocyanate were even smaller. Subjects with high perchlorate, high thiocyanate, and low iodine combined (n=62) had thyroxine concentrations 12.9% lower (mean difference=1.07 μg/dl, 95% confidence interval=0.55–1.59) than subjects with low perchlorate, low thiocyanate, and adequate iodine (n=376). Potential confounders had little impact on results. Overall, these results suggest that concomitant exposure to perchlorate, thiocyanate, and low iodine markedly reduces thyroxine production. This highlights the potential importance of examining the combined effects of multiple agents when evaluating the toxicity of thyroid-disrupting agents. -- Highlights: ► Recent data suggest that essentially everyone in the US is exposed to perchlorate. ► Perchlorate exposure may be associated with lower thyroid hormone levels. ► Some groups may be more susceptible to

  20. Femtosecond laser surface structuring and oxidation of chromium thin coatings: Black chromium

    Energy Technology Data Exchange (ETDEWEB)

    Kotsedi, L., E-mail: Kotsedi@tlabs.ac.za [UNESCO-UNISA Africa Chair in Nanosciences-Nanotechnology, College of Graduate Studies, University of South Africa, Muckleneuk Ridge, P.O. Box 392, Pretoria (South Africa); Nanosciences African Network (NANOAFNET), iThemba LABS-National Research Foundation, 1 Old Faure Road, Somerset West 7129, P.O. Box 722, Somerset West, Western Cape (South Africa); Nuru, Z.Y. [UNESCO-UNISA Africa Chair in Nanosciences-Nanotechnology, College of Graduate Studies, University of South Africa, Muckleneuk Ridge, P.O. Box 392, Pretoria (South Africa); Nanosciences African Network (NANOAFNET), iThemba LABS-National Research Foundation, 1 Old Faure Road, Somerset West 7129, P.O. Box 722, Somerset West, Western Cape (South Africa); Mthunzi, P. [National Laser Centre, Council for Scientific and Industrial Research, 0001 Pretoria (South Africa); Muller, T.F.G. [University of the Western Cape, Physics Department, Bellville, 7535 Cape Town (South Africa); Eaton, S.M. [Physics Department, Politecnico di Milano, Piazza Leonardo Da Vinci, 32, 20133 Milano (Italy); Julies, B. [University of the Western Cape, Physics Department, Bellville, 7535 Cape Town (South Africa); Manikandan, E. [UNESCO-UNISA Africa Chair in Nanosciences-Nanotechnology, College of Graduate Studies, University of South Africa, Muckleneuk Ridge, P.O. Box 392, Pretoria (South Africa); Nanosciences African Network (NANOAFNET), iThemba LABS-National Research Foundation, 1 Old Faure Road, Somerset West 7129, P.O. Box 722, Somerset West, Western Cape (South Africa); Ramponi, R. [Physics Department, Politecnico di Milano, Piazza Leonardo Da Vinci, 32, 20133 Milano (Italy); Maaza, M. [UNESCO-UNISA Africa Chair in Nanosciences-Nanotechnology, College of Graduate Studies, University of South Africa, Muckleneuk Ridge, P.O. Box 392, Pretoria (South Africa); Nanosciences African Network (NANOAFNET), iThemba LABS-National Research Foundation, 1 Old Faure Road, Somerset West 7129, P.O. Box 722, Somerset West, Western Cape (South Africa)

    2014-12-01

    Highlights: • Oxidation of the chromium thin film to chromium oxide by femtosecond laser with a fundamental wavelength of 1064 nm. • Solar absorber from chromium oxide that low percentage reflectance. • Femtosecond laser oxidation, with a de-focused laser. • Chromium oxide formation by femtosecond laser in normal ambient. - Abstract: In view of their potential applications as selective solar absorbers, chromium coatings on float glass substrates were nano/micro structured by femtosecond laser in air. Raman and X-rays diffraction investigations confirmed the formation of an ultra-porous α-Cr{sub 2}O{sub 3} layer at the surface; higher is the input laser power, enhanced is the crystallinity of the α-Cr{sub 2}O{sub 3} layer. The α-Cr{sub 2}O{sub 3} layer with the Cr underneath it in addition to the photo-induced porosity acted as a classical ceramic–metal nano-composite making the reflectance to decrease significantly within the spectral range of 190–1100 nm. The average reflectance decreased from 70 to 2%.

  1. Femtosecond laser surface structuring and oxidation of chromium thin coatings: Black chromium

    International Nuclear Information System (INIS)

    Highlights: • Oxidation of the chromium thin film to chromium oxide by femtosecond laser with a fundamental wavelength of 1064 nm. • Solar absorber from chromium oxide that low percentage reflectance. • Femtosecond laser oxidation, with a de-focused laser. • Chromium oxide formation by femtosecond laser in normal ambient. - Abstract: In view of their potential applications as selective solar absorbers, chromium coatings on float glass substrates were nano/micro structured by femtosecond laser in air. Raman and X-rays diffraction investigations confirmed the formation of an ultra-porous α-Cr2O3 layer at the surface; higher is the input laser power, enhanced is the crystallinity of the α-Cr2O3 layer. The α-Cr2O3 layer with the Cr underneath it in addition to the photo-induced porosity acted as a classical ceramic–metal nano-composite making the reflectance to decrease significantly within the spectral range of 190–1100 nm. The average reflectance decreased from 70 to 2%

  2. Production of basic chromium sulfate by using recovered chromium from ashes of thermally treated leather.

    Science.gov (United States)

    Dettmer, Aline; Nunes, Keila Guerra Pacheco; Gutterres, Mariliz; Marcílio, Nilson Romeu

    2010-04-15

    Leather wastes tanned with chromium are generated during the production process of leather, hence the wastes from hand crafted goods and footwear industries are a serious environmental problem. The thermal treatment of leather wastes can be one of the treatment options because the wastes are rich in chromium and can be used as a raw material for sodium chromate production and further to obtain several chromium compounds. The objective of this study was to utilize the chromium from leather wastes via basic chromium sulfate production to be subsequently applied in a hide tanning. The obtained results have shown that this is the first successful attempt to achieve desired base properties of the product. The result was achieved when the following conditions were applied: a molar ratio between sodium sulfite and sodium dichromate equal to 6; reaction time equal to 5 min before addition of sulfuric acid; pH of sodium dichromate solution equal to 2. Summarizing, there is an opportunity to utilize the dangerous wastes and reused them in the production scheme by minimizing or annulling the environmental impact and to attend a sustainable process development concept. PMID:20031309

  3. Inelastic Scattering of Neutrons in Chromium

    International Nuclear Information System (INIS)

    The phonon spectrum of chromium has been studied by neutron inelastic scattering. The dispersion curves are very similar, in form to those of tungsten and molybdenum, indicating similar interionic force constants. The neutron groups broaden but do not shift appreciably when the temperature is raised. No effect has been observed which can be attributed to the interaction between the phonons and the crystal magnetization in the antiferromagnetic phase. (author)

  4. Observational Approach to Chromium Site Remediation - 13266

    International Nuclear Information System (INIS)

    Production reactors at the U.S. Department of Energy's (DOE) Hanford Site in Richland, Washington, required massive quantities of water for reactor cooling and material processing. To reduce corrosion and the build-up of scale in pipelines and cooling systems, sodium dichromate was added to the water feedstock. Spills and other releases at the makeup facilities, as well as leaks from miles of pipelines, have led to numerous areas with chromium-contaminated soil and groundwater, threatening fish populations in the nearby Columbia River. Pump-and-treat systems have been installed to remove chromium from the groundwater, but significant contamination remain in the soil column and poses a continuing threat to groundwater and the Columbia River. Washington Closure Hanford, DOE, and regulators are working on a team approach that implements the observational approach, a strategy for effectively dealing with the uncertainties inherent in subsurface conditions. Remediation of large, complex waste sites at a federal facility is a daunting effort. It is particularly difficult to perform the work in an environment of rapid response to changing field and contamination conditions. The observational approach, developed by geotechnical engineers to accommodate the inherent uncertainties in subsurface conditions, is a powerful and appropriate method for site remediation. It offers a structured means of quickly moving into full remediation and responding to the variations and changing conditions inherent in waste site cleanups. A number of significant factors, however, complicate the application of the observational approach for chromium site remediation. Conceptual models of contamination and site conditions are difficult to establish and get consensus on. Mid-stream revisions to the design of large excavations are time-consuming and costly. And regulatory constraints and contract performance incentives can be impediments to the flexible responses required under the observational

  5. Stainless chromium-nickel steels. Chapter I

    International Nuclear Information System (INIS)

    The chemical composition is tabulated of 90 chromium-nickel stainless steels and alloys given in volume %. The values are also given of the corrosion resistance of the steels and alloys. The tables show data on the surface condition or the methods of material working, types and chemical composition of the medium where corrosion resistance tests were carried out, temperature, pressure, time of tests, corrosion rates, corrosion types, and literature references. A total of 35 references is given. (J.B.)

  6. Loading chromium atoms in a magnetic guide

    OpenAIRE

    Greiner, A; Sebastian, J.; Rehme, P.; Aghajani-Talesh, A.; Griesmaier, A.; Pfau, T.

    2007-01-01

    We have realized a magnetic guide for ultracold chromium atoms by continuously loading atoms directly from a Zeeman slower into a horizontal guide. We observe an atomic flux of $2 \\cdot 10^7$ atoms/s and are able to control the mean velocity of the guided atoms between 0 m/s and 3 m/s. We present our experimental results on loading and controlling the mean velocity of the guided atoms and discuss the experimental techniques that are used.

  7. X-616 Chromium Sludge Lagoons pictorial overview, Piketon, Ohio

    International Nuclear Information System (INIS)

    The Portsmouth Gaseous Diffusion Plant uses large quantities of water for process cooling. The X-616 Liquid Effluent Control Facility was placed in operation in December 1976 to treat recirculation cooling water blowdown from the process cooling system. A chromium-based corrosion inhibitor was used in the cooling water system. A chromium sludge was produced in a clarifier to control chromium levels in the water. Chromium sludge produced by this process was stored in two surface impoundments called the X-616 Chromium Sludge Lagoons. The sludge was toxic due to its chromium concentration and therefore required treatment. The sludge was treated, turning it into a sanitary waste, and buried in an Ohio EPA approved landfill. The plant's process cooling water system has changed to a more environmentally acceptable phosphate-based inhibitor. Closure activities at X-616 began in August 1990, with all construction activities completed in June 1991, at a total cost of $8.0 million

  8. Chromium oxidation state mapping in human cells

    Science.gov (United States)

    Ortega, R.; Fayard, B.; Salomé, M.; Devès, G.; Susini, J.

    2003-03-01

    The widespread use of chromium in industrial applications such as chemical production of pigments, refractory brick production, tanning, metallurgy, electroplating, and combustion of fuels has lead to human occupational exposure and to its increased introduction into the environment. Hexavalent chromium compounds are established carcinogens but their mechanism of cell transformation is not known. Up to now, no microanalytical technique was sensitive enough to allow the observation of chromium distribution, and oxidation state identification, within isolated cells at carcinogenic concentrations. In this experiment, we used successfully the ID-21 X-ray microscope to map Cr(VI) and total Cr distributions in cells exposed in vitro to soluble, and insoluble, Cr(VI) compounds. Exposure to soluble compounds, weak carcinogens, resulted in a homogeneous intracellular distribution of Cr, confirming by in situ measurement that Cr is present in the cell nucleus. Cr(VI) was never detected in cells which suggests a mechanism of rapid intracellular reducticn. On the other hand, exposure to insoluble compounds, strong carcinogens, also resulted in a homogeneous distribution of reduced forms of Cr in cells, and their nucleus. However, in this case, Cr(VI)-rich structures were observed into the cells suggesting that carcinogenicity is enhanced when oxidation reactions due to Cr(VI) chronic exposure are associated to Cr-DNA alterations.

  9. Dimensionally Controlled Lithiation of Chromium Oxide

    Energy Technology Data Exchange (ETDEWEB)

    Fister, Tim T. [Argonne National Lab. (ANL), Argonne, IL (United States); Hu, Xianyi [Northwestern Univ., Evanston, IL (United States); Esbenshade, Jennifer [Univ. of Illinois, Urbana-Champaign, IL (United States); Chen, Xiao [Northwestern Univ., Evanston, IL (United States); Wu, Jinsong [Northwestern Univ., Evanston, IL (United States); Dravid, Vinayak [Northwestern Univ., Evanston, IL (United States); Bedzyk, Michael [Northwestern Univ., Evanston, IL (United States); Long, Brandon [Argonne National Lab. (ANL), Argonne, IL (United States); Gewirth, Andrew A. [Univ. of Illinois, Urbana-Champaign, IL (United States); Shi, Bing [Argonne National Lab. (ANL), Argonne, IL (United States); Schlepütz, Christian M. [Argonne National Lab. (ANL), Argonne, IL (United States); Fenter, Paul [Argonne National Lab. (ANL), Argonne, IL (United States)

    2016-01-12

    Oxide conversion reactions are an alternative approach for high capacity lithium ion batteries but are known to suffer from structural irreversibility associated with the phase separation and reconstitution of reduced metal species and Li2O. In particular, the morphology of the reduced metal species is thought to play a critical role in the electrochemical properties of a conversion material. Here we use a model electrode with alternating layers of chromium and chromium oxide to better understand and control these phase changes in real-time and at molecular length scales. Despite lacking crystallinity at the atomic scale, this superstructure is observed (with X-ray reflectivity, XR) to lithiate and delithiate in a purely one-dimensional manner, preserving the layered structure. The XR data show that the metal layers act as nucleation sites for the reduction of chromium in the conversion reaction. Irreversibility during delithiation is due to the formation of a ternary phase, LiCrO2, which can be further delithiated at higher potentials. The results reveal that the combination of confining lithiation to nanoscale sheets of Li2O and the availability of reaction sites in the metal layers in the layered structure is a strategy for improving the reversibility and mass transport properties that can be used in a wide range of conversion materials.

  10. Chromium--a material for fusion technology

    International Nuclear Information System (INIS)

    Due to their low neutron-induced radioactivity chromium based materials are considered to be candidates for structure materials in fusion technology. In this paper investigations are presented of unirradiated chromium with a purity of 99.96% (DUCROPUR) and a dispersion strengthened chromium alloy Cr5Fe1Y2O3 (DUCROLLOY). Both materials have been produced in a powder metallurgical route. Mechanical tests of smooth and pre-cracked specimens have been performed in a wide temperature range. Below 280 deg. C the fracture toughness values of DUCROPUR are very low (1/2), above the transition temperature they exceed 500 MPa m1/2. Large plastic deformations have been observed. DUCROLLOY does not indicate such a significant increase of fracture toughness in the tested temperature range. But above 400 deg. C large plastic deformations can be obtained in bending samples, too. The fatigue crack propagation behaviour of DUCROPUR at 300 deg. C is similar to that of a ductile metal

  11. A REVIEW OF BIOSORPTION OF CHROMIUM IONS BY MICROORGANISMS

    OpenAIRE

    Inga Zinicovscaia

    2012-01-01

    Due to its widespread industrial use, chromium has become a serious pollutant in diverse environmental settings. The main source of chromium pollution including the Republic o Moldova is industry. It is a great need to develop new eco-friendly methods of chromium removal. Biosorption of heavy metals is a most promising technology involved in the removal of toxic metals from industrial waste streams and natural waters. This article is an extended abstract of a communication presented at the...

  12. CHROMIUM INDUCED CYTOTOXICITY IN BLACKGRAM (VIGNA MUNGO L.)

    OpenAIRE

    A. Chidambaram ، P. Sundaramoorthy ، A. Murugan ، K. Sankar Ganesh ، L. Baskaran

    2009-01-01

    Chromium is known to be highly toxic to biological systems. This study was designed to determine the mutagenic effects of different concentrations (0, 10, 25, 50, 100 and 200 mg/L) of hexavalent chromium on root tip cells of blackgram (Vigna mungo L. Hepper). The blackgram seeds were equi-spacially arranged in sterilized petriplates lined with filter paper and they were treated with different concentrations of chromium solution. In germination studies, the morphological growth parameters such...

  13. Processes affecting the remediation of chromium-contaminated sites.

    OpenAIRE

    Palmer, C.D.; Wittbrodt, P R

    1991-01-01

    The remediation of chromium-contaminated sites requires knowledge of the processes that control the migration and transformation of chromium. Advection, dispersion, and diffusion are physical processes affecting the rate at which contaminants can migrate in the subsurface. Heterogeneity is an important factor that affects the contribution of each of these mechanisms to the migration of chromium-laden waters. Redox reactions, chemical speciation, adsorption/desorption phenomena, and precipitat...

  14. Analysis of molybdenum, chromium, vanadium and iron by polarographic techniques

    International Nuclear Information System (INIS)

    The application of direct current Tast polarograph, differential pulse polarography and phase-selective alternative current Tast polarography to the problem of determining molybdenum, chromium, vanadium and iron in various supporting electrolytes is reported. The effect of the supporting electrolyte on the wave/peak potential and sensitivity of the metal ion have been examined. The polarographic methods were applied for simultaneous determination of chromium (3)/chromium (6), vanadium (4), vanadium (5) and iron (2)/iron (3) in different supporting electrolytes

  15. Production of a chromium Bose-Einstein condensate

    OpenAIRE

    Griesmaier, Axel; Stuhler, Jürgen; Pfau, Tilman

    2005-01-01

    The recent achievement of Bose-Einstein condensation of chromium atoms [1] has opened longed-for experimental access to a degenerate quantum gas with long-range and anisotropic interaction. Due to the large magnetic moment of chromium atoms of 6 {$\\mu$}B, in contrast to other Bose- Einstein condensates (BECs), magnetic dipole-dipole interaction plays an important role in a chromium BEC. Many new physical properties of degenerate gases arising from these magnetic forces have been predicted in ...

  16. Removal of chromium(VI) from saline wastewaters by

    OpenAIRE

    AKSU, Zümriye

    2002-01-01

    Some industrial wastewaters contain higher quantities of salts besides chromium(VI) ions so the effect of these salts on the biosorption of chromium(VI) should be investigated. The biosorption of chromium (VI) from saline solutions on two strains of living Dunaliella algae were tested under laboratory conditions as a function of pH, initial metal ion and salt (NaCl) concentrations in a batch system. The biosorption capacity of both Dunaliella strains strongly de...

  17. Increase of chromium utilization in stainless steel melting

    International Nuclear Information System (INIS)

    The processes of deoxidizing when melting stainless 18-10 steels in electric are furnaces by the method of remelting with wastes are investigated. The dependences of amount of reduced chromium on silicon consumption are made more precise. It is shown that it is useful to apply aluminium for deoxidation of acid high-chromium slags. Based on the data on pilot melts the extent to which aluminium can be used as a reducing agent for chromium is estimated. 3 refs., 2 figs

  18. Scientific Opinion on ChromoPrecise® cellular bound chromium yeast added for nutritional purposes as a source of chromium in food supplements and the bioavailability of chromium from this source

    OpenAIRE

    EFSA Panel on Food Additives and Nutrient Sources added to Food (ANS)

    2012-01-01

    The Panel on Food Additives and Nutrient Sources added to Food (ANS) provides a scientific opinion re-evaluating the safety of ChromoPrecise® cellular bound chromium yeast added for nutritional purposes as a source of chromium in food supplements and the bioavailability of chromium from this source. ChromoPrecise® is a yeast preparation with an enriched trivalent chromium content, obtained by culture of Saccharomyces cerevisiae in the presence of chromium chloride. A daily intake of 100 µg ch...

  19. Extraction-spectrophotometric determination of niobium with 1,2,4,6-tetraphenylpyridinium perchlorate and thiocyanate

    International Nuclear Information System (INIS)

    1,2,4,6-Tetraphenylpyridinium (TPP+) as the acetate or perchlorate was used as a counter ion in the spectrophotometric determination of Nb(V) by extraction into toluene of the anionic Nb(V) -thiocyanate complex from 4 to 6 M hydrochloric acid. The molar absorptivity of the ion-association complex, whose composition was shown to be NbOCl(SCN)3-.TPP+, was 2.82 x 104 l mol-1cm-1 at 395 nm. Beer's law was obeyed over the range 0.1 to 2.5 μg ml-1 of Nb(V). The method was applied to the determination of niobium in standard steels and ores with good precision and accuracy. 1-(4'-Nitrophenyl)-2,4,6-triphenylpyridinium (nitro-TPP+) perchlorate was also synthesised and used in the spectrophotometric determination of Nb(V), but did not show advantages over TPP+. The fluorescence of TPP+ and Nb(V)-SCN--TPP+ solutions in toluene also disappeared when nitro-TPP+ was used, owing to the paramagnetic effect of the NO2 group. (author)

  20. Interfacial behavior of perchlorate versus chloride ions in saturated aqueous salt solutions

    Energy Technology Data Exchange (ETDEWEB)

    Ghosal, S; Kuo, I W; Baer, M D; Bluhm, H

    2009-04-14

    In recent years combination of theoretical and experimental work have presented a novel view of the aqueous interface wherein hard and/or multiply charged ions are excluded from the interface, but large polarizable anions show interfacial enhancement relative to the bulk. The observed trend in the propensity of anions to adsorb at the air/water interface appears to be reverse of the Hofmeister series for anions. This study focuses on experimental and theoretical examination of the partitioning behavior of perchlorate (ClO{sub 4}{sup -}) and chloride (Cl{sup -}) ions at the air/water interface. We have used ambient pressure X-ray photoelectron spectroscopy technique to directly probe the interfacial concentrations of ClO{sub 4}{sup -} and Cl{sup -} ions in sodium perchlorate and sodium chloride solutions, respectively. Experimental observations are compared with first principles molecular dynamics simulations. Both experimental and simulation results show enhancement of ClO{sub 4}{sup -} ion at the interface, compared with the absence of such enhancement in the case of Cl{sup -} ion. These observations are in agreement with the expected trend in the interfacial propensity of anions based on the Hofmeister series.

  1. 123Iodine scintigraphy and perchlorate discharge test in the diagnosis of congenital hypothyroidism

    International Nuclear Information System (INIS)

    Aim: Thirty eight children suffering from congenital primary permanent hypothyroidism were studied to determine the diagnostic impact of 123I scintigraphy in comparison to laboratory findings and ultrasonography. Methods: In all patients 123I scintigraphy was performed after intravenous administration of 3,7 MBq 123I. If accumulation of the radiotracer in thyroid tissue occured a perchlorate discharge test was performed subsequently. Results: Scintigraphy revealed athyrosis in 7 children. In 9 children a lingual thyroid was observed. Deficiency in iodine organification was diagnosed by a significant discharge of 123I in 15 patients. In four of these children the diagnosis of Pendred's syndrome could be established. Ectopic thyroid tissue could be demonstrated only by scintigraphy where clinical examination and sonography failed in the diagnosis in all cases. Hypoplasia of the thyroid gland as it was diagnosed in 2 cases by ultrasonography appeared to be unlikely because of normal 123I uptake was seen in these patients. In 2 patients with scintigraphic proven athyrosis an orthotopic gland had been falsely considered by ultrasound. In 44% of our patients the final diagnosis could only be established if 123I scintigraphy and perchlorate discharge test were performed. Conclusion: This findings suggest that scintigraphy is indispensible in the correct diagnostic work up of congenital hypothyroidism. (orig.)

  2. Sol-gel preparation of a di-ureasil electrolyte doped with lithium perchlorate

    International Nuclear Information System (INIS)

    Solid polymer electrolytes (SPEs) synthesized by the sol-gel process and designated as di-ureasils have been prepared through the incorporation of lithium perchlorate, LiClO4, into the d-U(2000) organic-inorganic hybrid network. Electrolytes with lithium salt compositions of n (where n indicates the number of oxyethylene units per Li+ ion) between ∞ and 0.5 were characterized by conductivity measurements, cyclic voltammetry at a gold microelectrode, thermal analysis and Fourier transform Raman (FT-Raman) spectroscopy. The conductivity results obtained suggest that this system offers a quite significant improvement over previously characterized analogues doped with lithium triflate [S.C. Nunes, V. de Zea Bermudez, D. Ostrovskii, M.M. Silva, S. Barros, M.J. Smith, R.A. Sa Ferreira, L.D. Carlos, J. Rocha, E. Morales, J. Electrochem. Soc. 152 (2) (2005), A429]. 'Free' perchlorate ions, detected in all the samples examined, are identified as the main charge carriers in the sample that yields the highest room temperature conductivity (n = 20). In the di-ureasils with n ≤ 10 ionic association is favoured and the ionic conductivity drops

  3. Nano-Ammonium Perchlorate: Preparation, Characterization, and Evaluation in Composite Propellant Formulation

    Science.gov (United States)

    Kumari, A.; Mehilal; Jain, S.; Jain, M. K.; Bhattacharya, B.

    2013-07-01

    Nanomaterials are finding applications in explosives and propellant formulations due to their large surface area and high surface energy. This high surface energy is responsible for the low activation energy and increase in burning rate of the composition. Therefore, a successful attempt has been made to prepare nano-ammonium perchlorate using a nonaqueous method by dissolving ammonium perchlorate (AP) in methanol followed by adding the dissolved AP to the hydroxyl-terminated polybutadiene (HTPB), homogenization, and vacuum distillation of the solvent. The nano-AP thus formed was characterized using a NANOPHOX particle size analyzer (Sympatec, Germany), transmission electron microscopy (FEI, Hillsboro, OR), X-ray diffraction (PANalytical B.V., The Netherlands) and scanning electron microscopy (Ikon Analytical Equipment Pvt. Ltd., Mumbai, India) for particle size, purity, and morphology, respectively. The thermal behavior of nano-AP was also studied using differential thermal analysis-thermo gravimetric analysis (DTA-TGA). The data indicated that the particle size of the prepared AP was in the range of 21-52 nm and the thermal decomposition temperature was lower than that of coarse AP. Characterized nano-AP was subsequently used in composite propellant formulation up to 5% with 86% solid loading and studied for different properties. The results showed a 14% increase in burning rate in comparison to standard propellant composition with desired mechanical properties.

  4. Chromium depletion from stainless steels during vacuum annealing

    International Nuclear Information System (INIS)

    The behaviour of chromium during selective evaporation by high temperature vacuum annealing has been investigated by means of energy dispersive X-ray analysis and by neutron activation analysis. It was established that the rate of chromium loss from austenitic stainless steels 316 and 321 is controlled by chromium inter-diffusion rather than tracer diffusion in the alloy. Two important parameters in selective removal of chromium from alloy steels are the variation in the chromium surface concentration with time and the depletion profile in the alloy. The present work gives support for the model in which loss of chromium is dependent on its diffusivity in the alloy and on an interface transfer coefficient. The results showed that the surface concentration of chromium decreased with increasing vacuum annealing time. The chromium depletion profile in the metal was in accord with the previous derived model, apart from an anomalous near surface region. Here the higher resolution of a neutron activation technique indicated a region within approximately 2 microns of the surface where the chromium concentration decreased more steeply than expected. (author)

  5. Stabilization and solidification of chromium-contaminated soil

    Energy Technology Data Exchange (ETDEWEB)

    Cherne, C.A.; Thomson, B.M. [Univ. of New Mexico, Albuquerque, NM (United States). Civil Engineering Dept.; Conway, R. [Sandia National Labs., Albuquerque, NM (United States)

    1997-11-01

    Chromium-contaminated soil is a common environmental problem in the United States as a result of numerous industrial processes involving chromium. Hexavalent chromium [Cr(VI)] is the species of most concern because of its toxicity and mobility in groundwater. One method of diminishing the environmental impact of chromium is to reduce it to a trivalent oxidation state [Cr(III)], in which it is relatively insoluble and nontoxic. This study investigated a stabilization and solidification process to minimize the chromium concentration in the Toxicity Characteristic Leaching Procedure (TCLP) extract and to produce a solidified waste form with a compressive strength in the range of 150 to 300 pounds per square inch (psi). To minimize the chromium in the TCLP extract, the chromium had to be reduced to the trivalent oxidation state. The average used in this study was an alluvium contaminated with chromic and sulfuric acid solutions. The chromium concentration in the in the in situ soil was 1212 milligrams per kilogram (mg/kg) total chromium and 275 mg/kg Cr(VI). The effectiveness of iron, ferrous sulfate to reduce Cr(VI) was tested in batch experiments.

  6. Tribological Characteristics of Chromium-active Carbon Electroplated Composite Coatings

    Institute of Scientific and Technical Information of China (English)

    GUKa-fi; HUAMeng; Yi-min

    2004-01-01

    A process of chromium electroplating using a standard bath with additives and active carbon particles was reported, and the tribological behaviors of the composite coatings using the pin-on-disk tester and the table wear tester were i nvestig(aed. Experimental results indicate that the electroplated chromium-active carbon composite coatings exhibited the low friction coefficient anti excellent anti-wear properties whets coffered with the normal chromium electroplated ones. The formation of active carbon particles within the chromium matrices can be explained by SEM analysis and the mechanis of wear resistance of the composite coatings were studied.

  7. Defect transformation in GSGG crystals during chromium ion activation

    International Nuclear Information System (INIS)

    Absorption and induced absorption spectra, dose dependence of induced absorption, thermoluminescence of GSGG crystals, nominally pure and activated with chromium and neodymium ions in different concentrations, are investigated. It is shown that it is chromium ion presence in large concentration that decreases the induced coloration in GSGG crystals after γ-irradiation at 300 K. Optimum concentration of chromium ions for the minimum of induced coloration are found. The mechanism of decrease of induced coloration consisting in Fermi level displacement by chromium ion activation is established. Defect concentration and localization and recombination possibilities of electrons and holes in GSGG crystals are estimated by computer simulation

  8. Oral bioavailability of chromium from a specific site.

    OpenAIRE

    Witmer, C M; Harris, R.; Shupack, S I

    1991-01-01

    Analysis of soil from a specific site in New Jersey indicated a low level of sodium and chromium present as a calcium compound. Chromium was then administered orally to young, mature male rats at a level of 240 micrograms/kg for 14 days as chromium-contaminated soil, as CaCrO4, and as an equimolar mixture of the soil and calcium salts for 14 days. The rats were sacrificed 24 hr after the last dosing, and tissues were taken immediately for chromium analysis. Blood, muscle, and liver contained ...

  9. MICRO-SEGREGATION OF CHROMIUM IN Fe-Cr ALLOY

    OpenAIRE

    Igata, N.; Sato, S; ANDO, T.; H. Doi; Nishikawa, O.; Shibata, M.

    1984-01-01

    The objective of this investigation is to clarify the behavior of chromium atoms in iron-5at.% chromium alloy. When the specimens were quenched after soultion annealing at 1150°C for 1hr, FIM image was only a bright area, but when they were tempered from 450°C to 650°C, both bright areas and dark areas were observed in the FIM image. In these quenched specimens there was microsegregation of chromium atoms : In bright areas the chromium concentration was lower, and in dark areas it was higher ...

  10. Influence of Chelating Agents on Chromium Fate in Sediment

    Institute of Scientific and Technical Information of China (English)

    WANGXIAOCHANG; SUNJINHE; 等

    1996-01-01

    A laboratory investigation on reaction between chelating agents and chromium was conducted to evaluate the effect of chelating agents on the adsorption and desorption of chromium in sediment.The amount of adsorbed chromium(VI) in sediment decreased slightly by 5%-10% because of addition of chelating agents.Chelating agents inhibited the removal of Cr(Ⅲ)by sediment from solutions and the inhibiting effect was in the order:citric acid>tartaric acid>EDTA,Salicylic acid.No effect of chelating agents on desorption of chromium in sediment was observed.

  11. Analysing the chromium-chromium multiple bond using multiconfigurational quantum chemistry

    OpenAIRE

    Brynda, Marcin; Gagliardi, Laura; Roos, Björn O.

    2009-01-01

    This Letter discusses the nature of the chemical bond between two chromium atoms in different di-chromium complexes with the metal atoms in different oxidation states. Starting with the Cr diatom, with its formally sextuple bond and oxidation number zero, we proceed to analyse the bonding in some Cr(I)–Cr(I) XCrCrX complexes with X varying from F, to Phenyl, and Aryl. The bond distance in these complexes varies over a large range: 1.65–1.83 Å and we suggest explanations for these variations. ...

  12. The effect of chromium picolinate on serum cholesterol and apolipoprotein fractions in human subjects.

    OpenAIRE

    Press, R. I.; Geller, J.; Evans, G. W.

    1990-01-01

    Chromium has been implicated as a cofactor in the maintenance of normal lipid and carbohydrate metabolism. A deficiency of chromium results from diets low in biologically available chromium. Picolinic acid, a metabolite of tryptophan, forms stable complexes with transitional metal ions, which results in an improved bioavailability of the metal ion chromium. To determine whether or not chromium picolinate is effective in humans, 28 volunteer subjects were given either chromium tripicolinate (3...

  13. Reversible, Selective Trapping of Perchlorate from Water in Record Capacity by a Cationic Metal-Organic Framework.

    Science.gov (United States)

    Colinas, Ian R; Silva, Rachel C; Oliver, Scott R J

    2016-02-16

    We report the capture of ppm-level aqueous perchlorate in record capacity and kinetics via the complete anion exchange of a cationic metal-organic framework. Ambient conditions were used for both the synthesis of silver 4,4'-bipyridine nitrate (SBN) and the exchange, forming silver 4,4'-bipyridine perchlorate (SBP). The exchange was complete within 90 min, and the capacity was 354 mg/g, representing 99% removal. These values are greater than current anion exchangers such as the resins Amberlite IRA-400 (249 mg/g), Purolite A530E (104 mg/g), and layered double hydroxides (28 mg/g). Moreover, unlike resins and layered double hydroxides, SBN is fully reusable and displays 96% regeneration to SBN in nitrate solution, with new crystal formation allowing the indefinite cycling for perchlorate. We show seven cycles as proof of concept. Perchlorate contamination of water represents a serious health threat because it is a thyroid endocrine disruptor. This noncomplexing anionic pollutant is significantly mobile and environmentally persistent. Removal of other anionic pollutants from water such as chromate, pertechnetate, or arsenate may be possible by this methodology. PMID:26765213

  14. Anomalous aryl strengthening of americium and europium complexes during extraction by alkylenediphosphine dioxides from perchloric acid media

    International Nuclear Information System (INIS)

    Extraction of americium and europium from perchlorate environments by solutions of three types of methylenediphosphine dioxides, namely (C6H5)P(O)(CH2)sub(n)(O)P(C6H5)2, (C6H5)2P(O)CH2(O)P(C8H17)2 and (C8H17)2P(O)(CH2)sub(n)(O)P(C8H17)2 has been studied (n is 1 or 2 ) The diluents used have been dichlorethane and chloroform. In perchlorate environments the distribuiton coefficients of americium and europium have proved to be by about 3 orders of magnitude higher than in nitric acid environments, i.e. in perchlorate media the complexes are far more stable. Separation coefficients of americium and REE in perchloric acid soutions are much higher than in nitrate environments. The average value of Am/Eu separation coeffecient at 1-5 M acidity was about 6 (with dichlorethane as diluent) or about 7 (with chloroform as diluent). The complexes essentially exist as trisolvated. Americium complexes display anomalous stability increase upon being diluted: by about 2 orders of magnitude with dichlorethane and by up to 3 orders of magnitude with chloroform used as diluent

  15. The Effect of Chromium Added into Basal Diet on Serum Total Protein, Urea, Triglyceride, Cholesterol and Serum and Tissue Chromium, Zinc, Copper Levels in Rabbits

    OpenAIRE

    *, Kâzim ŞAHİN; *, Talat GÜLER; +, N. ŞAHİN; *, O. N. ERTAS; +, N. ERKAL

    1999-01-01

    This study was conducted to determine the effect of supplemantal dietary chromium on serum total protein, urea, triglycerides, cholesterol, and serum and tissue chromium, zinc, and copper contents of pregnant rabbits, their offspring and their young rabbits. Treatment groups consisted of chromium level as follows: Control Group no supplementation chromium into basal diet, Treatment I (200 ppb Group) contained 200 ppb of supplemental chromium into basal diet, and Treatment II (400 ppb Group...

  16. STABILITY AND ABSORPTION OF CHROMIUM AND ABSORPTION OF CHROMIUM HISTIDINE BY HUMANS

    Science.gov (United States)

    Increased intake of chromium has been shown to lead to improvements in glucose, insulin, lipids, and related variables in studies involving humans, experimental and farm animals. However, the results are often variable depending not only upon the selection of subjects, but also dietary conditions a...

  17. Chromium and Polyphenols From Cinnamon Improve Insulin Sensitivity

    Science.gov (United States)

    Naturally occurring compounds that have been shown to improve insulin sensitivity include chromium and polyphenols found in cinnamon. These compounds also have similar effects on insulin signaling and glucose control. The signs of chromium deficiency are similar to those for the metabolic syndrome ...

  18. IRIS Toxicological Review of Hexavalent Chromium (2010 External Review Draft)

    Science.gov (United States)

    [UPDATE] New Schedule for IRIS Hexavalent Chromium Assessment In Feb 2012, EPA developed a new schedule for completing the IRIS hexavalent chromium assessment. Based on the recommendations of the external peer review panel, which met in May 2011 to review the dra...

  19. Composition and structure of plasma sprayed chromium steel powders

    Czech Academy of Sciences Publication Activity Database

    Schneeweiss, O.; Voleník, Karel; Kolman, Blahoslav Jan

    Praha, 2005, s. 105-111. ISBN 1899072 18 7. [EURO Powder Metallurgy Congress & Exhibition. Prague (CZ), 02.10.2005-05.10.2005] Institutional research plan: CEZ:AV0Z20430508 Keywords : chromium steel * plasma spraying * chromium depletion * Mössbauer spectroscopy Subject RIV: JH - Ceramics, Fire-Resistant Materials and Glass

  20. Safety, absorption, and antioxidant effects of chromium histidine

    Science.gov (United States)

    Supplemental chromium has been shown to be involved in the alleviation of the metabolic syndrome, glucose intolerance, polycystic ovary syndrome, depression, excess body fat, and gestational, steroid-induced, and type 2 diabetes. Chromium amino acid complexes that contained histidine displayed cons...

  1. Toxicity and adaptation of Dictyosphaerium chlorelloides to extreme chromium contamination.

    Science.gov (United States)

    Sánchez-Fortún, Sebastián; López-Rodas, Victoria; Navarro, Macarena; Marvá, Fernando; D'ors, Ana; Rouco, Mónica; Haigh-Florez, David; Costas, Eduardo

    2009-09-01

    Metals are often spilled by industries into inland water environments, with adverse consequences. Numerous papers have reported that heavy metals produce massive destruction of algae. Nevertheless, algal populations seem to become tolerant when they have had previous exposures to heavy metals. Because the mechanisms allowing heavy metal tolerance of algae are not yet known, the present study analyzed the effect of hexavalent chromium on growth and photosynthetic performance of Dictyosphaerium chlorelloides, stressing on the adaptation mechanisms to chromium contamination. Growth and photosynthetic performance of algal cells were inhibited by Cr(VI) at 10 mg/L, and the 72-h median inhibition concentration was established as 1.64 and 1.54 mg/L, respectively. However, after further incubation for a three month period in an environment with 25 mg/L of chromium, some rare, chromium-resistant cells occasionally were found. A Luria-Delbrück fluctuation analysis was performed to distinguish between resistant algae arising from rare, spontaneous mutations and resistant algae arising from physiological adaptation and other adaptive mechanisms. Resistant cells arose only by spontaneous mutations before the addition of chromium, with a rate of 1.77 x 10(-6) mutants per cell division. From a practical point of view, the use of both chromium-sensitive and chromium-resistant genotypes could make possible a specific algal biosensor for chromium. PMID:19323601

  2. Residual Chromium in Leather by Instrumental Neutron Activation Analysis

    Directory of Open Access Journals (Sweden)

    S. Okoh

    2012-01-01

    Full Text Available Problem statement: Most tanning processes employ the use of chromium sulphate. For chromium tanned leather, finished products may contain high amount of residual chromium. This may pose some health hazards, since chromium is known to be toxic at elevated concentration. This justifies the need for the study. Approach: Various samples of leather were collected from a tannery, a leather crafts market, a leather dump site and from local tanners all in Kano, Nigeria in 2009. The samples were irradiated for 6 h in the inner site of the Nigerian Research Reactor (NIRR-1 at a flux of 5×1011 ncm-2 sec-1. Results: After evaluating the spectrum, the mean results for chromium in the samples were determined as 2.33±0.3, 2.23±0.3 and 2.93±0.4% for samples from the tannery, leather crafts market and leather dump sites respectively. Chromium concentration in samples collected from local tanners who use tannins from Acacia nilotica as tanning agent was below the detection limit of Instrumental Neutron Activation Analysis (INAA technique used in the study. Conclusion: Although, the concentrations of chromium in the analysed samples were not much higher than what were obtained in literature, they may be enough to sensitize the population that is allergic to chromium.

  3. AMORPHOUS ALLOY SURFACE COATINGS FOR HARD CHROMIUM REPLACEMENT - PHASE I

    Science.gov (United States)

    Hard chromium coatings (0.25 to10 mil thick) are used extensively for imparting wear and erosion resistance to components in both industrial and military applications. The most common means of depositing hard chromium has been through the use of chromic acid baths containing ...

  4. ADVANCES IN HEXAVALENT CHROMIUM REMOVAL AT HANFORD

    Energy Technology Data Exchange (ETDEWEB)

    NESHEM DO; RIDDELLE J

    2012-01-30

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

  5. Chromium-Makes stainless steel stainless

    Science.gov (United States)

    Kropschot, S.J.; Doebrich, Jeff

    2010-01-01

    Chromium, a steely-gray, lustrous, hard metal that takes a high polish and has a high melting point, is a silvery white, hard, and bright metal plating on steel and other material. Commonly known as chrome, it is one of the most important and indispensable industrial metals because of its hardness and resistance to corrosion. But it is used for more than the production of stainless steel and nonferrous alloys; it is also used to create pigments and chemicals used to process leather.

  6. The electronic structure of antiferromagnetic chromium

    DEFF Research Database (Denmark)

    Skriver, Hans Lomholt

    1981-01-01

    The author has used the local spin density formalism to perform self-consistent calculations of the electronic structure of chromium in the non-magnetic and commensurate antiferromagnetic phases, as a function of the lattice parameter. A change of a few per cent in the atomic radius brings...... the calculated ground state properties into agreement with experiment. The magnetisation is studied as function of volume in several models, and it is shown that a Stoner picture provides an extremely accurate description of the full calculation provided the sp-d hybridisation is taken into account. It is found...

  7. Determination of chromium content in potato by graphite furnace atomic absorption spectrometry%石墨炉原子吸收光谱法测定马铃薯中铬含量

    Institute of Scientific and Technical Information of China (English)

    向文军; 陈安银

    2014-01-01

    采用石墨炉原子吸收光谱法测定马铃薯中铬含量,采用了一种新的前处理方法(硝酸+硫酸+过氧化氢)的湿法消解法,并与传统湿法消解法(硝酸+高氯酸)作对比。结果表明,新的湿法消解法测得铬的含量略高于传统消解法测得铬的含量,加标回收率在92.7%~99.2%,精密度RSD为1.7135%,都优于传统的湿法消解法,避免了危险性较大的高氯酸,且反应温和,操作安全,简单,消解完全,结果准确,可以作为选择方法在实际工作中应用推广。%Graphite furnace atomic absorption spectrometry was used to determine content of chromium, and a comparison was made between a new wet digestion( nitric acid,hydrogen peroxide and sulfuric acid)and traditional wet digestion( nitric acid and perchloric acid)for pretreatment. The results showed that the content of Cr measured with new wet digestion method is slightly higher than that of traditional di-gestion method measured chromium,the recovery rate was 92. 7% ~99. 2% and RSD of precision was 1. 713 5%,the new wet digestion method is better than the traditional,the larger risk of perchloric acid was avoided,and the mild reaction conditions,safe operation,simple,complete digestion,accurate,and can be used as a selection method was applied in practical work.

  8. Effects of UV light and chromium ions on wood flavonoids

    International Nuclear Information System (INIS)

    The individual and simultaneous effect of UV light and chromium ions was investigated by spectrophotometric methods on inert surfaces impregnated with quercetin or robinetin. The UV-VIS spectra of the silica gel plates impregnated with these flavonoids were modified characteristically after irradiating ultraviolet light. Even a half an hour of irradiation has caused irreversible changes in the molecule structure. A certain chemical - presumably complexation - was concluded from the change of spectral bands assigned to flavonoids when impregnated with chromic ions. Hexavalent chromium caused more complex changes in the absorption spectra. The differences in the spectra could indicate either the oxidation and decomposition of flavonoids, or some kind of coordination process and the reduction of hexavalent chromium. The simultaneous application of UV light and chromium ions caused more pronounced effects. The complexation process between chromium(III) and flavonoid was completed

  9. CHROMIUM BIOACCUMULATION FROM COMPOSTS AND VERMICOMPOSTS BASED ON TANNERY SLUDGES

    Directory of Open Access Journals (Sweden)

    Krzysztof GONDEK

    2008-07-01

    Full Text Available Storage of waste substances is not indifferent to ecological equilibrium in the environment therefore should not be the ultimate way to limit waste arduousness. Therefore, the conducted investigations aimed to determine the effect of tannery composts and vermicomposts loaded with chromium on this element bioaccumulation in earthworm bodies and biomass of selected plants. Chromium in composts and vermicomposts based on tannery sludges occurred in small quantities and easily soluble compounds. Chromium concentrations in redworm biomass points to this metal accumulation in Eisenia fetida body tissues. This element content in redworm biomass was signifi cantly positively correlated with its content in composts. Chromium content in plants was diversifi ed and on treatments was generally smaller than on mineral treatment or farmyard manure. Chromium absorbed by plants was stored mainly in the root systems, and over the norm content of this element found in vermicomposts did not cause its excessive accumulation in plant biomass.

  10. Biosorption potency of Aspergillus niger for removal of chromium (VI).

    Science.gov (United States)

    Srivastava, Shaili; Thakur, Indu Shekhar

    2006-09-01

    Aspergillus niger isolated from soil and effluent of leather tanning mills had higher activity to remove chromium. The potency of Aspergillus niger was evaluated in shake flask culture by absorption of chromium at pH 6 and temperature 30 degrees C. The results of the study indicated removal of more than 75% chromium by Aspergillus niger determined by diphenylcarbazide colorimetric assay and atomic absorption spectrophotometry after 7 days. Study of microbial Cr(VI) reduction and identification of reduction intermediates has been hindered by the lack of analytical techniques that can identify the oxidation state with subcellular spatial resolution. Therefore, removal of chromium was further substantiated by transmission electron microscopy (TEM), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDX), which indicated an accumulation of chromium in the fungal mycelium. PMID:16874547

  11. Specific features of the electrocrystallization of chromium together with molybdenum

    International Nuclear Information System (INIS)

    A study was made on molybdenum effect on surface structure and some physicomechanical properties of electrolytic chromium during Cr-Mo electrodeposition from CrO3 solutions with additions of SO42- and SiFe62- anions. Cr-Mo deposition was conducted at 55 deg C and 0.5 A/cm2 current density which corresponds to conditions of hard chromizing. It is shown that the change hardness, hydridation and internal stresses of chromium coatings during their alloying with molybdenum is conditioned by structure change. Mo introduction into chromium is not manifested clearly in these characteristics. The change of chromium structure during deposition with molybdenum is probably related both with change of anion relation in cathode film (decrease of catalytic anion content in it) and peculiarities of chromium electrocrystallization. This requires special study with application of methods for investigation into fine and surface structure

  12. Effect of Triethanolamine and Benzaldehyde on the Storage Stability of Polystyrene- Ammonium Perchlorate Propellant

    Directory of Open Access Journals (Sweden)

    K. Kishore

    1986-10-01

    Full Text Available The effect of triethanolamine and benzaldehyde on the stability of polystyrene has been studied by dynamic thermogravimetry (TG. Slower decomposition of polymer in the presence of these compounds indicates their inhibiting ability on the oxidation of the polymer. The burning rate measurements of polystyrene (PS/ammonium perchlorate (AP propellants at ambient temperature and pressure shows an increase with the storage time. The percentage change in the burning rate of the propellants containing aldehyde and amine is less during the ageing which indicates the increased stability of the propellants. The safe-life time of the propellants for the ballistic stability has been calculated from the activation energy for the ageing process using an Arrhenius type equation. The safe-life of the propellants containing triethanolamine and benzaldehyde is more than the neat propellant.

  13. Potentiometric Electronic Tongue to Resolve Mixtures of Sulfide and Perchlorate Anions

    Directory of Open Access Journals (Sweden)

    Deivy Wilson

    2011-03-01

    Full Text Available This work describes the use of an array of potentiometric sensors and an artificial neural network response model to determine perchlorate and sulfide ions in polluted waters, by what is known as an electronic tongue. Sensors used have been all-solid-state PVC membrane selective electrodes, where their ionophores were different metal-phtalocyanine complexes with specific and anion generic responses. The study case illustrates the potential use of electronic tongues in the quantification of mixtures when interfering effects need to be counterbalanced: relative errors in determination of individual ions can be decreased typically from 25% to less than 5%, if compared to the use of a single proposed ion-selective electrode.

  14. Structure and properties of 2-cyanopyridinium perchlorate [2-CNPyH][ClO4

    Science.gov (United States)

    Czupinski, O.; Wojtas, M.; Zaleski, J.; Jakubas, R.; Medycki, W.

    2006-03-01

    The crystal structure of 2-cyanopyridinium perchlorate, [2-CNPyH][ClO4], has been determined at 100 (phase II) and 293 K (phase I). It is monoclinic P 21 at 100 K and orthorhombic P 212121 at 293 K. The dynamic properties of the crystal were studied by differential scanning calorimetry, dilatometry, pyroelectric, dielectric, proton (1H NMR), chlorine (35Cl NMR) magnetic resonance spectroscopies and the infrared method. The crystal undergoes a structural phase transition (\\mathrm {I\\rightarrow II} ) at 170 K characterized by a complex mechanism involving both 'order-disorder' and 'displacive' contributions. It reveals pyroelectric properties below 170 K. The dielectric relaxation existing over phase I is due to the motion of the cyano group, whereas the dynamics of the [ClO4]- anions is reflected in the significant dielectric increment around the \\mathrm {I\\rightarrow II} phase transition.

  15. Structure and properties of 2-cyanopyridinium perchlorate [2-CNPyH][ClO4

    International Nuclear Information System (INIS)

    The crystal structure of 2-cyanopyridinium perchlorate, [2-CNPyH][ClO4], has been determined at 100 (phase II) and 293 K (phase I). It is monoclinic P 21 at 100 K and orthorhombic P 212121 at 293 K. The dynamic properties of the crystal were studied by differential scanning calorimetry, dilatometry, pyroelectric, dielectric, proton (1H NMR), chlorine (35Cl NMR) magnetic resonance spectroscopies and the infrared method. The crystal undergoes a structural phase transition (I →II) at 170K characterized by a complex mechanism involving both 'order-disorder' and 'displacive' contributions. It reveals pyroelectric properties below 170K. The dielectric relaxation existing over phase I is due to the motion of the cyano group, whereas the dynamics of the [ClO4]- anions is reflected in the significant dielectric increment around the I →II phase transition

  16. Degradation study of trichloroethylene and perchloric ethylene using high energy electron beam generated in industrial accelerator

    International Nuclear Information System (INIS)

    The pollution of potable water with chlorinated hydrocarbons, mainly trichloroethylene (TCE) and perchloric ethylene (PCE), is seriously increasing the problem of contamination of water, specially in highly industrialized areas. Recent studies show that depuration by ionizing radiation has been considered a possible alternative to the control of water pollution, wherein the process by ionizing radiation converts TCE and PCE into approximately 100% carbon dioxide ions. Water samples containing TCE e PCE were submitted to radiation in the pilot plant installed in the industrial electron accelerator at IPEN from Radiation Dynamics, Dynamitron II, of 1,5 MeV - 25 m A, with doses varying from 2 kGy to 8 kGy, being its parameters analyzed before and after irradiation TCE and PCE concentrations were determined by the gas chromatography method by liquid-liquid extraction using a gas chromatograph, model CG 90, with an electron capture detector. (author). 5 refs, 4 figs

  17. Thyroid scintigraphy and perchlorate discharge test in the diagnosis of congenital hypothyroidism

    International Nuclear Information System (INIS)

    Quantitative thyroid scanning using low doses of technetium-99m sodium pertechnetate was performed on 147 infants (55 males and 92 females) with congenital hypothyroidism detected through the national neonatal screening programme. Thirty-two (21.8%) were athyrotic, while 62 (42.2%) had an ectopic thyroid and 53 (36%) had a eutopic gland with increased 99mTc uptake (mean 17%; range, 5%-38%). The perchlorate discharge test (PDT) was performed in nine of the infants with ectopic glands and 15 with eutopic glands; the findings were consistent with an organification defect in 22 cases (seven ectopic and 15 eutopic). Thyroid scintigraphy and PDT can add useful aetiological, genetic and prognostic information in the clinical evaluation of infants with congenital hypothyroidism detected by neonatal screening. (orig.). With 4 figs., 1 tab

  18. Promethium-147 extraction with 1,1-diantipyrylalkanes from perchlorate solutions

    International Nuclear Information System (INIS)

    Conditions for quantitative extraction of indicator amounts of promethium-147 from perchlorate solutions with 1,1-diantipyrylalkanes are found. The composition of oxtracted complexes is identified. Extraction concentration constants are calculated. The dependence between the extraction capacity and reagent structure is established. Promethium-147 is used as a radioactive label when studying La3+, Ce3+, Pr3+, Nd3+, Sm3+, Lu3+ extraction. The concentration constants of r.e.e. extraction with diantipyrylmethane are 3.1x1010; 3.5x1010; 3.5x1010; 3.8x1010; 4.0x1010; 6.2x1010, respectively, when μ=0.2

  19. Non-aqueous titrimetric assay of gabapentin in capsules using perchloric acid as titrant

    Directory of Open Access Journals (Sweden)

    SAMEER A.M. ABDULRAHMAN

    2011-06-01

    Full Text Available Two simple, rapid, accurate and inexpensive methods using visual and potentiometric titrimetric techniques are described for the determination of gabapentin (GBP in bulk drug as well as in capsules. The methods are based on the neutralization reaction of the primary amino group of GBP with acetous perchloric acid as titrant in anhydrous acetic acid medium. The end point was detected either visually using crystal violet as indicator or potentiometrically using a modified glass electrode SCE electrode system. Both methods are applicable over the range 1.0-16.0 mg of GBP and the titration reaction follows a 1:1 stoichiometry. The methods were successfully applied to the determination of GBP in capsules. The validity of the proposed methods was further ascertained by parallel determination by a reference method and by recovery studies via standard-addition technique.

  20. Thyroid scintigraphy and perchlorate discharge test in the diagnosis of congenital hypothyroidism

    Energy Technology Data Exchange (ETDEWEB)

    El-Desouki, M. [Dept. of Medicine, King Saud Univ., Riyadh (Saudi Arabia); Al-Jurayyan, N. [Dept. of Paediatrics, King Saud Univ., Riyadh (Saudi Arabia); Al-Nuaim, A. [Div. of Endocrinology, King Saud Univ., Riyadh (Saudi Arabia); Al-Herbish, A. [Dept. of Paediatrics, King Saud Univ., Riyadh (Saudi Arabia); Abo-Bakr, A. [Dept. of Paediatrics, King Saud Univ., Riyadh (Saudi Arabia); Al-Mazrou, Y. [Ministry of Health, Riyadh (Saudi Arabia); Al-Swailem, A. [Ministry of Health, Riyadh (Saudi Arabia)

    1995-09-01

    Quantitative thyroid scanning using low doses of technetium-99m sodium pertechnetate was performed on 147 infants (55 males and 92 females) with congenital hypothyroidism detected through the national neonatal screening programme. Thirty-two (21.8%) were athyrotic, while 62 (42.2%) had an ectopic thyroid and 53 (36%) had a eutopic gland with increased {sup 99m}Tc uptake (mean 17%; range, 5%-38%). The perchlorate discharge test (PDT) was performed in nine of the infants with ectopic glands and 15 with eutopic glands; the findings were consistent with an organification defect in 22 cases (seven ectopic and 15 eutopic). Thyroid scintigraphy and PDT can add useful aetiological, genetic and prognostic information in the clinical evaluation of infants with congenital hypothyroidism detected by neonatal screening. (orig.). With 4 figs., 1 tab.

  1. Effect of Microwave Heating on the Leaching of Lateritic Nickel Ore in Perchloric Acid

    International Nuclear Information System (INIS)

    In this study, the leaching conditions of Sivrihisar (Adatepe) limonite type lateritic ore in acidic medium were investigated. Leaching experiments were carried out using conventional and microwave-assisted method. The effects of stirring speed, leaching temperature, perchloric acid concentration, solid/liquid ratio and particle size on conventional leaching were determined. Microwave-assisted leaching was carried out by using the optimum results of the conventional leaching. The pre-heating process was applied on different microwave powers (0, 90, 180, 360 and 600 W) and pre-processing time (0, 1, 3, 5, 7, 10, 15 and 20 min). These experimental results demonstrated that acid leaching was a convenient method for Ni extraction from lateritic ore. The higher dissolution and the higher Ni recoveries in the microwave-assisted leaching process were obtained in less leach time. (author)

  2. Hydration of some trivalent metal ions extracted as perchlorates with trioctylphosphine oxide in hexane

    International Nuclear Information System (INIS)

    Perchlorates of Sc3+, Y3+, La3+, and Eu3+ have each been extracted from 0.1 mol x dem-3 aqueous solution of μ=1 with trioctylphosphine oxide (TOPO) in hexane. The hydration number of the extracted salts has been determined by Karl Fischer titration. Sc3+, Y3+, and Eu3+ are extracted as the tetra- and hexa-solvates of TOPO but the assumption of octa-solvate on addition to the tetra-solvate explains the extraction data of La3+ well. The hydration number of tetra-solvates is 2(Sc3+ and Eu3+), 3(Y3+) and probably 4 for La3+ ion. That of hexa-and octa-solvates is 4-5. (author)

  3. Hydration and Solvation of Metal Perchlorates Extracted with Trioctylphosphine Oxide in Hexane

    International Nuclear Information System (INIS)

    Perchlorates of Sc3+, Y3+, La3+, and Eu3+ have each been extracted from 0.1 mol dm-3 aqueous solution of μ=1 with trioctylphosphine oxide (TOPO) in hexane. The hydration number of the extracted salts has been determined by Karl Fischer titration. Sc3+, Y3+, and Eu3+ are extracted as the tetra- and hexa-solvates of TOPO but the assumption of octa-solvate on addition to the tetra-solvate explains the extraction data of La3+ well. The hydration number of tetra-solvates is 2 (Sc3+ and Eu3+), 3 (Y3+) and probably 4 for La3+ ion. That of hexa-and octa- solvates is 4-5. (author). 1 tabs

  4. Extraction of lanthanide and scandium perchlorates by podands bearing diphenylphosphorylacetamide terminal groups

    International Nuclear Information System (INIS)

    Interphase distribution of La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu,Y and Sc perchlorate trace amounts between HClO4 aqueous solutions and phosphorus-containing podands with two end groups Ph2P(O)CH2C(O)NH- connected by di- and triethylene glycol chain in dichlorethane has been studied. Stoichiometry of extracted complexes is determined, effect of HClO4 concentration in aqueous phase and nature of organic solvent on the efficiency of metal ion transitions in organic phase are treated. Studied compounds reveal higher extraction ability regarding to metal ions in HClO4 solutions as compared with the same ability of (dibutylcarbamoylmethyl)diphenylphosphine oxide. Possibility for the using macroporous polymer sorbents impregnated by studied podands for the separation and concentration of rare earth(III) and Sc(III) ions from aqueous solutions containing ClO4- anions has been demonstrated

  5. A Consideration for Design of Ammonium Perchlorate/Hydroxyl Terminated Polybutadiene Composite Propellant

    Science.gov (United States)

    Kohga, Makoto

    Specific impulse and burning rate characteristics are the important properties for the propellant design. Because of the requirements for the preparation of ammonium perchlorate (AP)/hydroxyl-terminated polybutadiene (HTPB) composite propellant, there is an upper limit content, φ of AP contained propellant. Specific impulse and burning rate increase with increasing the AP content. The specific impulse, Ispφ and the burning rate, rφ of the propellant prepared at φ, rφ are the highest values of the propellant prepared with AP used as an oxidizer. It is necessary for the propellant design to estimate φ, Ispφ and rφ. The φ, Ispφ and rφ are closely associated with the specific surface area, Swp measured by air-permeability method. Therefore, these values are estimated with Swp. A process for the design of AP/HTPB composite propellant would be proposed in this study.

  6. Large Angular Jump Mechanism Observed for Hydrogen Bond Exchange in Aqueous Perchlorate Solution

    Energy Technology Data Exchange (ETDEWEB)

    Ji, Minbiao; /SLAC, PULSE /Stanford U., Phys. Dept.; Odelius3, Michael; /Stockholm U.; Gaffney1, K.J.; /aff SLAC, PULSE

    2010-06-11

    The mechanism for hydrogen bond (H-bond) switching in solution has remained subject to debate despite extensive experimental and theoretical studies. We have applied polarization-selective multidimensional vibrational spectroscopy to investigate the H-bond exchange mechanism in aqueous NaClO{sub 4} solution. The results show that a water molecule shifts its donated H-bonds between water and perchlorate acceptors by means of large, prompt angular rotation. Using a jump-exchange kinetic model, we extract an average jump angle of 49 {+-} 4{sup o}, in qualitative agreement with the jump angle observed in molecular dynamics simulations of the same aqueous NaClO{sub 4} solution.

  7. Complexes of rare-earth perchlorates with ditbutyl amides of di, tri and tetraglycolic acids

    OpenAIRE

    Premlatha, C; Soundararajan, S

    1981-01-01

    New complexes of lanthanide perchlorates with di-t-butyl amides of di, tri and tetraglycolic acids have been synthesised. The complexes have the general formula Ln(DiGA)3(ClO4)3; Ln(TriGA)2 (ClO4)3 and Ln(TetGA)2 (C1O4)3, where Ln = La-Yb and Y and DiGA = N,N′, di-t-butyl diglycolamide, TriGA N,N′, di-t-butyl triglycolamide and TetGA = N,N′ di-t-butyl tetraglycolamide, respectively. The complexes have been characterized by analysis, electrolytic conductance, infrared,1H and13C nuclear magneti...

  8. Effect of Perchlorates on Electron Radiolysis of Glycine with Application to Mars

    Science.gov (United States)

    Góbi, Sándor; Abplanalp, Matthew J.; Kaiser, Ralf I.

    2016-05-01

    This work explores the radiolytic decomposition of glycine (H2NCH2COOH) under simulated Martian conditions in the presence of perchlorates ({{{ClO}}4}-), which are abundant oxidizers on the surface of Mars, by energetic electrons at 10, 160, 210, and 260 K, mimicking the radiation exposure of the Martian regolith in the first 5-10 cm depths over about 250 million years. Our experiments present quantitative evidence that the rate constants of the glycine decomposition in the presence of magnesium perchlorate hexahydrate (Mg(ClO4)2 · 6H2O) were a factor of about two higher than that of the pure glycine, suggesting that energetic oxygen atoms (O) released from the {{{ClO}}4}- have a significant effect on the decomposition rates and accelerate them by providing a unique oxidizing environment in the radiolyzed samples. Hence, two decay mechanisms exist: radiolysis by the electrons and oxidation by the O atoms. Within the Mars-relevant temperature range covering 160-260 K, the destruction rates are nearly temperature invariant with rates varying as little as 5%. Further, the formation rates of carbon dioxide (CO2) and carbon monoxide (CO) are both accelerated in the presence of {{{ClO}}4}- by a factor of three to five, supporting our conclusion of an active oxygen-initiated chemistry. In addition, the degradation rates are significantly higher than the formation rates of CO2 and CO. This suggests that, besides the decarboxylation, alternative degradation pathways such as a polymerization of glycine must exist. Finally, besides CO2 and CO, three alternative products were identified tentatively: methylamine (CH3NH2), methane (CH4), and ammonia (NH3).

  9. Selenium protection from cadmium and chromium poisoning

    International Nuclear Information System (INIS)

    The interaction of selenium with cadmium and chromium was studied in 168 chicken-broilers (DWCxWR) divided into four equal groups. Eight-week old control animals received an intravenous dose of /sup 115m/Cd Chloride 370 KBq/Kg (Group I), or 51Cr Chloride 370 KBq/Kg (Group II). The kinetics of these isotopes were studied by scintillation spectrometry (NaI/TI) carried out for whole blood, plasma, plasma proteins, urine, feces and homogenates of all organs at various time intervals. Animals in Groups III and IV received eight subcutaneous doses of sodium selenate (5ug) at 8-week intervals prior to /sup 115m/Cd or 51Cr. The kinetics of these elements were studied as in the previous two groups. It was found that selenium affected those kinetics in two ways: (a) by increasing the excretion of Cd by 11 +/- 3% (P < 0.001) and that of Cr by 7 +/- 1% (P < 0.001); and (b) by favoring redistribution of those elements, with significant (P < 0.001) reductions in liver, endocrine glands and kidney and increases (P < 0.01) in bone. The study suggests that selenium protects the animals' vital organs from environmental pollutants, such as cadmium and chromium

  10. The hydrogen anode in chromium electrowinning

    International Nuclear Information System (INIS)

    The use of a hydrogen anode for electrowinning of chromium from an ammonium chromium sulfate electrolyte (chrome alum process) was investigated in a laboratory-scale cell equipped with a diaphragm. The composition of the solution and the temperature followed industrial practice. Current density, pH, and anolyte flow rate through the diaphragm were varied and optimized for the cell. For a cathodic current density of 915 A/m2 at 50oC, the optimum initial pH was 2.37. The hydrogen anode was made of a platinized Toray carbon paper (0.35 mg Pt per cm2) supplied by E-TEK. The hydrogen pressure was maintained at 2 cm H20 above ambient atmosphere. The potential of the hydrogen anode was about 1 V lower than that of a Pb-Ag anode (1%Ag) in a similar cell. As expected, no Cr+6 was generated in the anolyte. The cathodic current efficiency was slightly lower with the hydrogen anode than with the Pb-Ag anode. (author)

  11. Biliary excretion of chromium in the rat

    International Nuclear Information System (INIS)

    The relative amount of chromium excreted in rat bile after injection of Cr-III is much less than after injection of Cr-VI, about 0.1% and from 6-8% during 5 hours respectively, for corresponding dose levels. The liver to bile ratio was 50-100 for Cr-III injection for Cr-VI the ratio was 2-3. With doses up to 18 μmol Cr/kg, only Cr-III was found in bile even after injection of CR-VI.Glutathione depletion of the liver with cyclohexene oxide decreased chromium excretion in bile. Such treatment also decresed the reduction of Cr-VI to Cr-III in the liver cell as only Cr-VI was found in bile. A different distribution of Cr-III in the liver dependent on whether derived from Cr-VI or taken up by the liver as such must be assumed. Taking into account the usual low penetration of biological membranes by Cr-III, a possible active transport mechanism or a specific diffusable Cr-III compound must be postulated. (author)

  12. METHOD 332.0: DETERMINATION OF PERCHLORATE IN DRINKING WATER BY ION CHROMATOGRAPHY WITH SUPPRESSED CONDUCTIVITY AND ELECTROSPRAY IONIZATION MASS SPECTROMETRY

    Science.gov (United States)

    This method is applicable to the identification and quantitation of perchlorate in raw and finished drinking waters. The approach used is ion chromatography with suppressed conductivity and electrospray ionization mass spectrometry (IC-ESI/MS)

  13. Thermal Diffusivity and Specific Heat Measurements of Titanium Potassium Perchlorate Titanium Subhydride Potassium Perchlorate 9013 Glass 7052 Glass SB-14 Glass and C-4000 Muscovite Mica Using the Flash Technique.

    Energy Technology Data Exchange (ETDEWEB)

    Specht, Paul Elliott; Cooper, Marcia A.

    2015-02-01

    The flash technique was used to measure the thermal diffusivity and specific heat of titanium potassium perchlorate (TKP) ignition powder (33wt% Ti - 67wt% KP) with Ventron sup- plied titanium particles, TKP ignition powder (33wt% Ti - 67wt% KP) with ATK supplied titanium particles, TKP output powder (41wt% Ti - 59wt% KP), and titanium subhydride potassium perchlorate (THKP) (33wt% TiH 1.65 - 67wt% KP) at 25 o C. The influence of density and temperature on the thermal diffusivity and specific heat of TKP with Ventron supplied titanium particles was also investigated. Lastly, the thermal diffusivity and specific heats of 9013 glass, 7052 glass, SB-14 glass, and C-4000 Muscovite mica are presented as a function of temperature up to 300 o C.

  14. Workshop on effects of chromium coating on Nb3Sn superconductor strand: Proceedings

    International Nuclear Information System (INIS)

    This report discusses the following topics: Chromium coating on superconductor strand -- an overview; technology of chromium plating; comparison of wires plated by different platers; search for chromium in copper; strand manufactures' presentations; chromium plating at the Lawrence Livermore National Laboratory; a first look at a chromium plating process development project tailored for T.P.X. and I.T.E.R. strand; and influence of chromium diffusion and related phenomena on the reference ratios of bare and chromium plated Nb3Sn strand

  15. Stabilization of chromium salt in ordinary portland cement

    Indian Academy of Sciences (India)

    Damir Barbir; Pero Dabić; Petar Krolo

    2012-12-01

    Ordinary Portland cement (OPC) samples containing the chromium salt have been investigated using differential microcalorimetry, conductometry and Fourier transform infrared spectroscopic analysis. The effect of chromium on OPC hydration was evaluated by continuous observing of early hydration. The microcalorimetrical results show that with increasing the share of chromium salt, heat maximums assume lower values and the occurrence of the maximum registered in the earlier hydration times. Conductometrical measurements show that with increasing addition of chromium salt, curve did not show any specific shape, immediate drop in specific conductivity is noticed and the maximum is reached earlier. This coincides with microcalorimetrical results. It can be concluded that the addition of chromium does not affect the mechanism of the hydration process, but it does affect the kinetic parameters and dynamics of the cement hydration process. It was found that chromium salt addition to the cement–water system is acceptable up to 2 wt.%. According to standard EN 196-3 for OPC, the beginning of binding time should occur after 60 minutes. Increased amount of chromium over 2 wt.% significantly accelerate the beginning of binding time and for the system it is not acceptable.

  16. Chromium speciation in rainwater: temporal variability and atmospheric deposition

    Energy Technology Data Exchange (ETDEWEB)

    Kieber, R.J.; Willey, J.D.; Zvalaren, S.D. [University of North Carolina at Wilmington, Wilmington, NC (United States). Dept. of Chemistry

    2002-12-15

    Chromium is released into the atmosphere by a variety of anthropogenic activities which include steel manufacturing, leather tanning, wood presentation and fossil fuel combustion. The concentrations of the various chromium species were determined in 89 rainwater samples collected in Wilmington, NC from October 1, 1999 to December 31, 2001. Volume weighted annual average concentrations of Cr{sub total}, particulate Cr, Cr(III)(aq), and Cr(VI)(aq) were 4.6, 2.2, 0.8 and 1.2 nM, respectively. There was distinct seasonal and diurnal variability in the concentrations of the various chromium species. Chromium emissions to the global atmosphere by both natural and anthropogenic sources are estimated to be 2.2 x 10{sup 9} mol/yr. Using rainwater concentration data along with other published rainwater Cr concentrations and an estimate for total global annual rain, the total global flux of chromium removed from the atmosphere via wet deposition is 2.1 x 10{sup 9} mol/yr. This represents complete removal of Cr and indicates that essentially all chromium released into the global atmosphere is removed via rain. About half this chromium is dissolved with roughly equal concentrations of toxic Cr(VI) and relatively harmless Cr(III) species. 48 refs., 4 figs., 3 tabs.

  17. Bioavailability of a potato chromium complex to the laboratory rat

    International Nuclear Information System (INIS)

    Research objectives were to study the effect of food source, preparation method and chemical form on bioavailability of chromium. Chromium concentration in potatoes was determined and tubers labeled either intrinsically or extrinsically with radioactive chromate. A labeled chromium complexes was isolated from preparations of raw, baked or fried potatoes and chromatographed on gel permeation media. Availability of the potato chromium complex to the rat was examined in three feeding studies. Animals were dosed with radioactive extrinsically or intrinsically labeled potato extract or with chromate. A labeled chromium complex was isolated from gastrointestinal contents of rats and chromatographed. Potato pulp and peel contained 1.63 and 2.70 μg Cr/g tissue respectively. True and apparent absorption from extrinsically labeled feedings were 33.4 +/- 4.7 and 29.8 +/- 11.2% respectively, and no differences existed between absorption from raw and cooked potatoes. Absorption from the extrinsic labeled potatoes differed significantly from absorption of inorganic chromatium. Apparent absorption of raw (11.1 +/- 7.9%) and cooked (-0.7 +/- 2.8%) intrinsically labeled feedings differed significantly. Absorption of inorganic chromium was 17.8% (true) and 11.5% (apparent). Examination of the chromium complex isolated from gastrointestinal tract contents showed enlargement of the complex in the stomach after consumption

  18. Chromium-induced membrane damage: protective role of ascorbic acid

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Importance of chromium as environmental toxicant is largely due to impact on the body to produce cellular toxicity. The impact of chromium and their supplementation with ascorbic acid was studied on plasma membrane of liver and kidney in male Wistar rats (80 - 100gbody weight). It has been observed that the intoxication with chromium ( i. p. ) at the dose of 0.8 mg/100g body weight per day for a period of 28 days causes significant increase in the level of cholesterol and decrease in the level of phospbolipid of both liver and kidney. The alkaline pbosphatase, total ATPase and Na + -K + -ATPase activities were significantly decreased in both liver and kidney after chromium treatment,except total ATPase activity of kidney. It is suggested that chromium exposure at the present dose and duration induce for the alterations of structure and function of both liver and kidney plasma membrane. Ascorbic acid ( i.p. at the dose of 0.5 mg,/100g body weight per day for period of 28 days) supplementation can reduce these structural changes in the plasma membrane of liver and kidney. But the functional changes can not be completely replenished by the ascorbic acid supplementation in response to chromium exposure. So it is also suggested that ascorbic acid (nutritional antioxidant) is useful free radical scavenger to restrain the chromium-induced membrane damage.

  19. Fertilizers and Mixed Crop Cultivation of Chromium Tolerant and Sensitive Plants under Chromium Toxicity

    OpenAIRE

    B. Dheeba; Sampathkumar, P; Kannan, K.

    2015-01-01

    Zea mays (maize) and Vigna radiata (green gram) are found to be the chromium (Cr) tolerant and sensitive plants, respectively. In the present paper, we investigate the reduction of the toxicity of Cr in the sensitive plants by the mixed crop cultivation in the field using various amendments. Further, the potassium dichromate was used as the source of hexavalent Cr. The results indicated that Cr adversely affects both the growth and yield of plants. The soil properties vary with Cr and differe...

  20. Microbial Diversity of Chromium-Contaminated Soils and Characterization of Six Chromium-Removing Bacteria

    Science.gov (United States)

    He, Zhiguo; Hu, Yuting; Yin, Zhen; Hu, Yuehua; Zhong, Hui

    2016-06-01

    Three soil samples obtained from different sites adjacent to a chromium slag heap in a steel alloy factory were taken to examine the effect of chromium contamination on soil bacterial diversity as determined by construction of 16S rDNA clone libraries and sequencing of selected clones based on restriction fragment length polymorphism (RFLP) analysis. Results revealed that Betaproteobacteria, Gammaproteobacteria, Firmicutes, and Alphaproteobacteria occurred in all three soil samples, although the three samples differed in their total diversity. Sample 1 had the highest microbial diversity covering 12 different classes, while Sample 3 had the lowest microbial diversity. Strains of six different species were successfully isolated, one of which was identified as Zobellella denitrificans. To our knowledge, this is the first report of a strain belonging to the genus Zobellella able to resist and reduce chromium. Among all isolates studied, Bacillus odysseyi YH2 exhibited the highest Cr(VI)-reducing capability, with a total removal of 23.5 % of an initial Cr(VI) concentration of 350 mg L-1.

  1. Chromium removal from tannery wastewater by using of flying ash

    International Nuclear Information System (INIS)

    A simple and economic method to chromium removal from tannery wastewater by means of flying ash is presented. The chromium removal operation is a discontinuous process that involve the mass of flying ash, time of contact and temperature or ph as variables, their which are optimized through Box-Wilson type experimental design. The results were successful: From an initial fluid whit chromium concentration of 1850m ppm, final concentrations of 0.008 ppm and 0.5 ppm of Cr+3 and Cr+6 respectively were achieved. These post-treatment concentrations are into the approved range definite by Government's Laws to this waste type

  2. A REVIEW OF BIOSORPTION OF CHROMIUM IONS BY MICROORGANISMS

    Directory of Open Access Journals (Sweden)

    Inga Zinicovscaia

    2012-12-01

    Full Text Available Due to its widespread industrial use, chromium has become a serious pollutant in diverse environmental settings. The main source of chromium pollution including the Republic o Moldova is industry. It is a great need to develop new eco-friendly methods of chromium removal. Biosorption of heavy metals is a most promising technology involved in the removal of toxic metals from industrial waste streams and natural waters. This article is an extended abstract of a communication presented at the Conference Ecological Chemistry 2012

  3. Poly[[tetrakis(μ2-pyrazine N,N′-dioxide-κ2O:O′erbium(III] tris(perchlorate

    Directory of Open Access Journals (Sweden)

    James D. Buchner

    2010-09-01

    Full Text Available The title three-dimensional coordination network, {[Er(C4H4N2O24](ClO43}n, is isostructural to that of other lanthanides. The Er+3 cation lies on a fourfold roto-inversion axis. It is coordinated in a distorted square-antiprismatic fashion by eight O atoms from bridging pyrazine N,N′-dioxide ligands. There are two unique pyrazine N,N′-dioxide ligands. One ring is located around an inversion center, and there is a a twofold rotation axis at the center of the other ring. There are also two unique perchlorate anions. One is centered on a twofold rotation axis and the other on a fourfold roto-inversion axis. The perchlorate anions are located in channels that run perpendicular to (001 and (110 and interact with the coordination network through C—H...O hydrogen bonds.

  4. Bis(μ-bis{[4-(2-pyridylpyrimidin-2-yl]sulfanyl}methanedisilver(I bis(perchlorate

    Directory of Open Access Journals (Sweden)

    Hai-Bin Zhu

    2010-12-01

    Full Text Available In the macrocyclic centrosymmetric dinuclear complex, [Ag2(C19H14N6S22](ClO42, the AgI atom, bis{[4-(2-pyridylpyrimidin-2-yl]sulfanyl}methane (2-bppt ligand and perchlorate anion each lie on a twofold rotation axis. The 2-bppt ligand chelates two four-coordinated AgI atoms through its two bipyridine-like arms. The O atoms of the perchlorate anion are disordered each over two positions of equal occupancy. Adjacent complex molecules are linked by π–π interactions between the pyridine and pyrimidine rings [centroid–centroid distance = 3.663 (8 Å].

  5. Poly[[tetrakis(μ2-pyrazine N,N′-dioxide-κ2O:O′holmium(III] tris(perchlorate

    Directory of Open Access Journals (Sweden)

    James D. Buchner

    2010-09-01

    Full Text Available The title three-dimensional coordination network, {[Ho(C4H4N2O24](ClO43}n, is isostructural to that of other lanthanides. The Ho+3 cation lies on a fourfold roto-inversion axis. It is coordinated in a distorted square anti-prismatic fashion by eight O atoms from bridging pyrazine N,N′-dioxide ligands. There are two unique pyrazine N,N′-dioxide ligands. One ring is located around an inversion center, and there is a a twofold rotation axis at the center of the other ring. There are also two unique perchlorate anions. One is centered on a twofold rotation axis and the other on a fourfold roto-inversion axis. The perchlorate anions are located in channels that run perpendicular to (001 (110 and interact with the coordination network through C—H...O hydrogen bonds.

  6. Thermal incorporation behavior during the reduction and stabilization of chromium wastes

    OpenAIRE

    Yang, Jun; 楊駿

    2015-01-01

    The possibility of employing periclase to stabilize chromium in chromium wastes into spinel-based ceramics through thermal method was investigated by heating mixture of simulated chromium waste and magnesium oxide. Different types of magnesium oxide precursors were introduced to incorporate chromium oxide into magnesiochromite (MgCr2O4) ranging from 550 ºC to 1350 ºC. Magnesium oxide precursors of both types can effectively incorporate chromium oxide but via different mechanisms. Three main f...

  7. Effects of Supplemental Dietary Chromium on Yield and Nutrient Digestibility of Laying Hens Under Low Temperature

    OpenAIRE

    ŞAHİN, Kazım; ERTAŞ, O. Nihat; GÜLER, Talat; ÇİFTÇİ, Mehmet

    2001-01-01

    This study was conducted to determine the effects of chromium picolinate (CrPi) added into diet containing 710.3 ppb chromium on yield and nutrient digestibility of laying hens at low temperature. Forty-six-week-old laying hens were randomly assigned to four groups of 30 hens per group. Treatment groups were fed different supplemental dietary chromium levels. Thus, hens were fed diets with no supplemental chromium (Control Group), 100 ppb of supplemental chromium (100 Group), 200 ppb of s...

  8. Evaluation of the comprehensiveness and reliability of the chromium composition of foods in the literature ☆

    OpenAIRE

    Thor, Mayly Y.; Harnack, Lisa; King, Denise; Jasthi, Bhaskarani; Pettit, Janet

    2011-01-01

    In the early 1960s, trivalent chromium Cr3+ became recognized as an essential trace element due to its potential metabolic and cardiovascular benefits. No comprehensive chromium database currently exists; thus a thorough review of the literature was conducted to examine the availability and reliability of chromium data for foods. A number of key issues were identified that challenge the feasibility of adding chromium to a food and nutrient database. Foremost, dietary chromium data reported in...

  9. Chromium(III) complexation to natural organic matter : Mechanisms and modeling

    OpenAIRE

    Gustafsson, Jon Petter; Persson, I.; Oromieh, A. G.; Van Schaik, J. W. J.; Sjöstedt, Carin; Kleja, D. B.

    2014-01-01

    Chromium is a common soil contaminant, and it often exists as chromium(III). However, limited information exists on the coordination chemistry and stability of chromium(III) complexes with natural organic matter (NOM). Here, the complexation of chromium(III) to mor layer material and to Suwannee River Fulvic Acid (SRFA) was investigated using EXAFS spectroscopy and batch experiments. The EXAFS results showed a predominance of monomeric chromium(III)-NOM complexes at low pH (<5), in which o...

  10. Abatement of Chromium Emissions from Steelmaking Slags - Cr Stabilization by Phase Separation

    OpenAIRE

    Albertsson, Galina

    2013-01-01

    Chromium is an important alloying element in stainless steel but also environmentally harmful element. A number of mineralogical phases present in the slag matrix can contain chromium and lead to chromium leaching. Chromium in slag if not stabilized, could oxidize to the cancerogenic hexavalent state, and leach out if exposed to acidic and oxygen rich environment. Other environmental concerns are slag dusting and chromium escape to the atmosphere. Despite the fact that there is a certain risk...

  11. The oxidation and reduction of chromium of stainless steels in an eletric arc furnace

    OpenAIRE

    Arh, B.; F. Tehovnik

    2011-01-01

    The oxidation of chromium during the elaboration of stainless steels occurs with oxygen in solution blown inthe melt and with oxides in the slag. A higher content of silicon in the furnace charge decreases the extent of oxidation of chromium, however, the efficient reduction of chromium from the slag is of essential importance for a minimal loss of chromium. In this survey, the theory of the oxidation of chromium, its reduction from the slag and the conditions for the formation of foaming sla...

  12. Chromium accumulation, microorganism population and enzyme activities in soils around chromium-containing slag heap of steel alloy factory

    Institute of Scientific and Technical Information of China (English)

    HUANG Shun-hong; PENG Bing; YANG Zhi-hui; CHAI Li-yuan; ZHOU Li-cheng

    2009-01-01

    The environmental risk of chromium pollution is pronounced in soils adjacent to chromate industry. It is important to investigate the functioning of soil microorganisms in ecosystems exposed to long-term contamination by chromium. 45 soil samples obtained from different places of the slag heap in a steel alloy factory were analyzed for chromium contamination level and its effect on soil microorganisms and enzyme activities. The results show that the average concentrations of total Cr in the soil under the slag heap, adjacent to the slag heap and outside the factory exceed the threshold of Secondary Environmental Quality Standard for Soil in China by 354%, 540% and 184%, respectively, and are 15, 21 and 9 times higher than the local background value, respectively. Elevated chromium loadings result in changes in the activity of the soil microbe, as indicated by the negative correlations between soil microbial population and chromium contents. Dehydrogenase activity is greatly depressed by chromium in the soil. The results imply that dehydrogenase activity can be used as an indicator for the chromium pollution level in the area of the steel alloy factory.

  13. Evaluation of chromium in red blood cells as an indicator of exposure to hexavalent chromium: An in vitro study.

    Science.gov (United States)

    Devoy, Jérôme; Géhin, Antoine; Müller, Samuel; Melczer, Mathieu; Remy, Aurélie; Antoine, Guillaume; Sponne, Isabelle

    2016-07-25

    Chromium(VI) compounds are classified as carcinogenic to humans. Whereas chromium measurements in urine and whole blood (i.e., including plasma) are indicative of recent exposure, chromium in red blood cells (RBC) is attributable specifically to Cr(VI) exposure. Before recommending Cr in RBC as a biological indicator of Cr(VI) exposure, in-vitro studies must be undertaken to assess its reliability. The present study examines the relationship between the chromium added to a blood sample and that subsequently found in the RBC. After incubation of total blood with chromium, RBC were isolated, counted and their viability assessed. Direct analysis of chromium in RBC was conducted using Atomic Absorption Spectrometry. Hexavalent, but not trivalent Cr, was seen to accumulate in the RBC and we found a strong correlation between the Cr(VI) concentration added to a blood sample and the amount of Cr in RBC. This relationship appears to be independent of the chemical properties of the human blood samples (e.g., different blood donors or different reducing capacities). Even though in-vivo studies are still needed to integrate our understanding of Cr(VI) toxicokinetics, our findings reinforce the idea that a single determination of the chromium concentration in RBC would enable biomonitoring of critical cases of Cr(VI) exposure. PMID:27178267

  14. The fate of chromium during tropical weathering

    DEFF Research Database (Denmark)

    Berger, Alfons; Frei, Robert

    2014-01-01

    We performed a mineral, geochemical and Cr–Sr–Pb isotope study on a laterite profile developed on ca. 540 Ma old tonalitic bedrock in Madagascar with special emphasis on the behavior of chromium during tropical weathering. The observed strong depletions of Ca, Si, and P, and enrichment of Fe and Al...... weathering profile. The negatively fractionated δ53Cr values measured in the weathering profile relative to the unaltered tonalitic bedrock characterized by a high temperature magmatic inventory Cr isotope signature are consistent with loss of a positively fractionated Cr(VI) pool formed during weathering...... highly oxidative conditions, which in well drained sulfide-bearing parent bedrocks potentially lead to both, acid dissolution of sulfide-hosted Cr and redox-promoted mobilization of Cr(VI) from silicates during later stages of weathering under basic pH conditions....

  15. Neutron capture by the chromium isotopes

    International Nuclear Information System (INIS)

    Capture cross sections of the chromium isotopes have been measured at neutron energies up to 350 keV using the capture cross section facility at the 40 m station of the Oak Ridge Electron Linear Accelerator. Parameters have been derived for 180 resonances. A moderate correlation [rho(gamma-n-0,gamma-gamma) approximately 0.45] is observed between reduced neutron widths and radiative widths for s-wave resonances. Calculations of valence widths show that valence capture can only account for the correlated component of the observed radiative widths. An additional mechanism such as a 2p-1h doorway state must therefore be occurring to explain the uncorrelated component. (author)

  16. Reactions between cerium(IV) and methyl-6-x-derivatives of aniline in perchloric acid solutions

    International Nuclear Information System (INIS)

    The oxidation of 2,6-dimethyl-, 2-isopropyl-6-methyl, 2-chloro-6-methyl-and 2-methyl-6-nitro aniline with cerium(IV) in perchloric acid solutions has been examined. It has been found that the concentration of hydrogen ions and the basicity of nitrogen atom in the amine group decide about the resultant intermediate products. Some of these products can be practically prepared using cerium(IV) as an oxidizing agent. (author). 16 refs, 1 tab

  17. X-ray, vibrational spectra and quantum chemical studies on a new semiorganic crystal: 4-Chloroanilinium perchlorate

    Science.gov (United States)

    Anitha, R.; Athimoolam, S.; Gunasekaran, M.; Anitha, K.

    2014-11-01

    A new semi-organic material 4-chloroanilinium perchlorate was synthesized and grown as a single crystal by slow evaporation solution growth technique. A good X-ray quality single crystal was selected from the grown crops and used for the single crystal diffraction studies. The asymmetric part of the unit cell contains a 4-chloroanilinium cation and a perchlorate anion. The protonation on the N site of the chloroaniline is confirmed from the CN bond distance and the deprotonation on perchloric acid is confirmed from ClO bond geometry. The molecular aggregations are stabilized through intricate three dimensional hydrogen bonding network formed by the classical NH⋯O hydrogen bonds. It form two infinite chains running along the b-axis of the unit cell which are cross-linked through another NH⋯O bond leading to alternate ring R44(12) motifs. These ring and chain motifs lead to alternate hydrophilic and hydrophobic layers along c-axis of the unit cell. The presence of different functional groups and the nature of their vibrations were identified in experimental vibrational studies through Infra-Red and Raman measurements in the range of 4000-400 cm-1. The optimized molecular structure, vibrational mode, computed spectra, molecular properties and NBO analysis of the 4-chloroanilinium perchlorate were found out by quantum chemical calculations with HF and DFT/B3LYP methods invoking 6-311++G(d,p) basis sets. Computed geometrical parameters and harmonic frequencies of fundamental, combination and overtone transitions were found in satisfactory agreement with the experimental data. The electronic properties such as HOMO and LUMO energies were carried out.

  18. Evaluation of the Protective Effects of Emilia sonchifolia Linn. (DC.) on Perchlorate-Induced Oxidative Damage

    OpenAIRE

    D. Gayathri Devi; Y. Lija; T.R. Cibin; Biju, P.G.; V. Gayathri Devi; Annie Abraham

    2006-01-01

    Emilia sonchifolia Linn. (DC.) is a traditionally used medicinal plant seen in most tropical and subtropical regions worldwide. Various parts of the plant are used for the treatment of diseases like asthma, intermittent fevers, breast cancer, ophthalmia, nyctalopia etc. We have isolated the flavonoid fraction from E. sonchifolia (whole plant). Female albino rats were fed with 0.2% sodium perchlorate to induce oxidative stress. The flavonoid fraction of the plant was fed along with sodium perc...

  19. 2,5-Bis[2-({bis[3-(dimethylazaniumylpropyl]azaniumyl}methylphenyl]-1,3,4-oxadiazole hexakis(perchlorate sesquihydrate

    Directory of Open Access Journals (Sweden)

    Vieri Fusi

    2012-12-01

    Full Text Available In the title hydrated salt, C36H66N8O6+·6ClO4−·1.5H2O, the asymmetric unit consists of a hexaprotonated [H6L]6+ cation, five perchlorate anions in general positions, two on twofold rotation axes (one of which is disordered, and two water molecules of crystallization in general positions, one of them disordered around a twofold crystallographic axis. In the [H6L]6+ cation, two strong intramolecular N—H...N hydrogen bonds occur, involving the N atoms of the oxadiazole ring as acceptors and the closest NH+ groups of each dipropylenetriamine unit. In the crystal, the [H6L]6+ cations form channels along the a-axis direction, in which the perchlorate counter-ions and the water molecules are lodged. The crystal packing features a network of N—H...O and O—H...O hydrogen bonds involving the NH+ groups of the [H6L]6+ cation, the perchlorate anions and the water molecules.

  20. Microbial respiration with chlorine oxyanions: diversity and physiological and biochemical properties of chlorate- and perchlorate-reducing microorganisms.

    Science.gov (United States)

    Liebensteiner, Martin G; Oosterkamp, Margreet J; Stams, Alfons J M

    2016-02-01

    Chlorine oxyanions are valuable electron acceptors for microorganisms. Recent findings have shed light on the natural formation of chlorine oxyanions in the environment. These suggest a permanent introduction of respective compounds on Earth, long before their anthropogenic manufacture. Microorganisms that are able to grow by the reduction of chlorate and perchlorate are affiliated with phylogenetically diverse lineages, spanning from the Proteobacteria to the Firmicutes and archaeal microorganisms. Microbial reduction of chlorine oxyanions can be found in diverse environments and different environmental conditions (temperature, salinities, pH). It commonly involves the enzymes perchlorate reductase (Pcr) or chlorate reductase (Clr) and chlorite dismutase (Cld). Horizontal gene transfer seems to play an important role for the acquisition of functional genes. Novel and efficient Clds were isolated from microorganisms incapable of growing on chlorine oxyanions. Archaea seem to use a periplasmic Nar-type reductase (pNar) for perchlorate reduction and lack a functional Cld. Chlorite is possibly eliminated by alternative (abiotic) reactions. This was already demonstrated for Archaeoglobus fulgidus, which uses reduced sulfur compounds to detoxify chlorite. A broad biochemical diversity of the trait, its environmental dispersal, and the occurrence of relevant enzymes in diverse lineages may indicate early adaptations of life toward chlorine oxyanions on Earth. PMID:26104311

  1. Chromium and Polyphenols from Cinnamon and Insulin Sensitivity

    Science.gov (United States)

    Factors that improve insulin sensitivity usually lead to improvements in risk factors associated with the metabolic syndrome, diabetes, and cardiovascular diseases. Naturally occurring bioactive compounds that have been shown to improve insulin sensitivity include chromium and polyphenols found in ...

  2. Contingency plans for chromium utilization. Publication NMAB-335

    International Nuclear Information System (INIS)

    The United States depends entirely on foreign sources for the critical material, chromium, making it very vulnerable to supply disruptions. This vulnerability results because chromium is essential for the fabrication of corrosion-resisting steels and high-temperature, oxidation-resisting alloys in applications that are vital to the nation's technological well-being; because no substitutes are known for these materials in those applications; and because the known, substantial deposits of chromite ore are only in a few geographical locations that could become inaccessible to the United States as a result of political actions. The effectiveness of programs such as stockpiling, conservation, and research and development for substitutes to reduce the impact of disruption of imports of chromite and ferrochromium are discussed. Alternatives for decreasing chromium consumption also are identified for chromium-containing materials in the areas of design, processing, and substitution

  3. Synthesis and characterization of novel chromium pillared clays

    International Nuclear Information System (INIS)

    New chromium pillared clays of basal spacing 2.45 nm were synthesized and characterized. The chromium oligomers used for intercalation were prepared by quick addition of base and acid to Cr(III) monomeric solutions followed by reflux. The synthesized clays exhibit increased BET surface area and higher micropore volume compared to clays with lower galleries, pillared either by smaller Cr(III) oligomers or by Cr(III) monomers. Important parameters affecting the d001 basal spacing were studied, e.g. the pH of the pillaring solution, the intercalation time, the chromium concentration and the counter-anion present in the chromium solutions. Scanning electron micrographs were acquired to demonstrate changes of the clay texture before and after pillaring. The thermal behavior of the synthesized clays was also examined

  4. Adsorption Properties of Chromium (VI by Chitosan Coated Montmorillonite

    Directory of Open Access Journals (Sweden)

    Dahe Fan

    2006-01-01

    Full Text Available The adsorption of chromium (VI by Chitosan Coated Montmorillonite (CCM from aqueous solution was studied. To evaluate the adsorption capacity, the effects of pH, initial concentration and temperature on the adsorption were investigated. The isothermal data was applied to Langmuir linear and the Freundlich linear isotherm equation and the thermodynamic parameters (ΔH, ΔG, ΔS were calculated according to the values of binding Langmuir constant, KL. Results indicated that the adsorption between CCM and chromium (VI was significantly physical, the negative ΔH constant at lower temperature confirmed that the more chromium (VI was adsorbed by chitosan coated montmorillonite at lower temperature. The kinetics of the sorption process of chromium (VI on chitosan coated montmorillonite were investigated using the pseudo-first order and pseudo-second order kinetics, results showed that the pseudo-second order equation model provided the best correlation with the experimental results.

  5. IRIS Toxicological Review of Hexavalent Chromium (Peer Review Plan)

    Science.gov (United States)

    EPA is conducting a peer review of the scientific basis supporting the human health hazard and dose-response assessment of hexavalent chromium that will appear on the Integrated Risk Information System (IRIS) database.

  6. Fabrication of high rate chromium getter sources for fusion applications

    International Nuclear Information System (INIS)

    Design and fabrication techniques are described for the manufacture of large-capacity chromium getter sources, analogous to the commercially available titanium getter source known as Ti-Ball, manufactured by Varian Associates

  7. Detecting Grain-Boundary Chromium Depletion in Inconel 600

    Science.gov (United States)

    Airey, G. P.; Vaia, A. R.; Pessall, N.; Aspden, R. G.

    1981-11-01

    Techniques to evaluate grain-boundary chromium depletion in Inconel Alloy 600 were investigated. Procedures studied were a modified Huey test, reactivation polarization, magnetic permeability measurements, and eddy current measurements. Results from these tests were correlated with susceptibility to stress-assisted intergranular cracking in polythionic acid. Thermally treated Inconel Alloy 600 steam generator tubing was the principal source of material evaluated, but experimental heats of Ni-Cr-Fe alloys with 8-18 wt.% Cr were prepared to determine the critical chromium level below which stress-assisted intergranular cracking occurs; this critical chromium content was found to be between 9.8 and 11.7 wt.%. All four techniques were considered suitable to evaluate grain-boundary chromium depletion; the modified Huey test and reactivation polarization technique showed a greater sensitivity than the magnetic permeability and eddy current measurements.

  8. The diffusion of chromium in a duplex alloy steel

    International Nuclear Information System (INIS)

    Diffusion of chromium in a duplex stainless steel containing approximately 8% ferrite has been investigated in the temperature range 600 to 10000C using the standard serial sectioning technique. The resulting concentration profiles exhibited up to four distinct regions. The two main regions are attributed to volume diffusion in the austenite and ferrite phases, the other zones being due to short circuiting paths. Volume diffusion in the austenite phase is in good agreement with chromium diffusion in Type 316 steel. The chromium diffusion coefficient in the ferrite phase of approximate composition 25 wt % Cr, 5 wt % Ni is given by: Dsub(α) = (6.0(+11,-3)) x 10-6 exp - ((212+-5)/RT) m2s-1 the activation energy being expressed in kJ.mol-1. Little evidence was found for enhanced chromium diffusion along austenite/ferrite interface boundaries. (author)

  9. Chromium plating pollution source reduction by plasma source ion implantation

    International Nuclear Information System (INIS)

    There is growing concern over the environmental toxicity and workers' health issues due to the chemical baths and rinse water used in the hard chromium plating process. In this regard the significant hardening response of chromium to nitrogen ion implantation can be environmentally beneficial from the standpoint of decreasing the thickness and the frequency of application of chromium plating. In this paper the results of a study of nitrogen ion implantation of chrome plated test flats using the non-line-of-sight Plasma Source Ion Implantation (PSII) process, are discussed. Surface characterization was performed using Scanning Electron Microscopy (SEM), Auger Electron Spectroscopy (AES), and Electron Spectroscopy for Chemical Analysis (ESCA). The surface properties were evaluated using a microhardness tester, a pin-on-disk wear tester, and a corrosion measurement system. Industrial field testing of nitrogen PSII treated chromium plated parts showed an improvement by a factor of two compared to the unimplanted case

  10. New Chromium Carbonyl Catalysts for [6+2] Cycloaddition Reactions

    OpenAIRE

    Kundig, Ernst Peter; Robvieux, Fabrice; Kondratenko, Mikhail

    2002-01-01

    The complexes, (benzene)chromiumdicarbonyl(methyl acrylate) and chromiumdicarbonylbis(cyclohexadiene), are precursors for the highly coordinatively unsaturated chromium dicarbonyl fragment 3, a catalyst for the cycloaddition of activated olefins to cycloheptatriene.

  11. Removal of toxic ions (chromate, arsenate, and perchlorate) using reverse osmosis, nanofiltration, and ultrafiltration membranes

    KAUST Repository

    Yoon, Jaekyung

    2009-09-01

    Rejection characteristics of chromate, arsenate, and perchlorate were examined for one reverse osmosis (RO, LFC-1), two nanofiltration (NF, ESNA, and MX07), and one ultrafiltration (UF and GM) membranes that are commercially available. A bench-scale cross-flow flat-sheet filtration system was employed to determine the toxic ion rejection and the membrane flux. Both model and natural waters were used to prepare chromate, arsenate, and perchlorate solutions (approximately 100 μg L-1 for each anion) in mixtures in the presence of other salts (KCl, K2SO4, and CaCl2); and at varying pH conditions (4, 6, 8, and 10) and solution conductivities (30, 60, and 115 mS m-1). The rejection of target ions by the membranes increases with increasing solution pH due to the increasingly negative membrane charge with synthetic model waters. Cr(VI), As(V), and ClO4 - rejection follows the order LFC-1 (>90%) > MX07 (25-95%) ≅ ESNA (30-90%) > GM (3-47%) at all pH conditions. In contrast, the rejection of target ions by the membranes decreases with increasing solution conductivity due to the decreasingly negative membrane charge. Cr(VI), As(V), and ClO4 - rejection follows the order CaCl2 < KCl ≅ K2SO4 at constant pH and conductivity conditions for the NF and UF membranes tested. For natural waters the LFC-1 RO membrane with a small pore size (0.34 nm) had a significantly greater rejection for those target anions (>90%) excluding NO3 - (71-74%) than the ESNA NF membrane (11-56%) with a relatively large pore size (0.44 nm), indicating that size exclusion is at least partially responsible for the rejection. The ratio of solute radius (ri,s) to effective membrane pore radius (rp) was employed to compare ion rejection. For all of the ions, the rejection is higher than 70% when the ri,s/rp ratio is greater than 0.4 for the LFC-1 membrane, while for di-valent ions (CrO4 2 -, SO4 2 -, and HAsSO4 2 -) the rejection (38-56%) is fairly proportional to the ri,s/rp ratio (0.32-0.62) for the ESNA

  12. Perchlorate production by ozone oxidation of chloride in aqueous and dry systems

    International Nuclear Information System (INIS)

    Overwhelming evidence now exists that perchlorate is produced through natural processes and can be ubiquitously found at environmentally relevant concentrations in arid and semi-arid locations. A number of potential production mechanisms have been hypothesized and ClO4- production by ozone oxidation of surface bound Cl- was demonstrated. However, no information concerning the impact of concentration, final reaction products distribution, impact of reaction phase, or oxidation of important oxychlorine intermediates has been reported. Using IC-MS-MS analysis and replicate oxidation experiments, we show that exposing aqueous solutions or Cl- coated sand or glass surfaces to O3 (0.96%) generated ClO4- with molar yields of 0.007 and 0.01% for aqueous Cl- solutions and 0.025 and 0.42% for Cl- coated sand and glass, respectively. Aqueous solutions of Cl- produced less ClO4- than Cl- coated sand or glass as well as a higher ratio of ClO3- to ClO4-. Reduction of the initial Cl- mass resulted in substantially higher molar yields of ClO4- and ClO3-. In addition, alkaline absorbers that captured gaseous products contained substantial quantities of Cl-, ClO3-, and ClO4-. Solutions of possible oxychlorine intermediates (OCl- and ClO3-) exposed to O3 produced only scant amounts of ClO4- while a ClO2- solution exposed to O3 produced substantial molar yields of ClO4- (4% molar yield). Scanning electron microscopy coupled with energy energy-dispersive X-ray analysis demonstrated a significant loss of Cl- and an increase in oxygen on the Cl- coated silica sand exposed to O3. While the experimental conditions are not reflective of natural conditions this work clearly demonstrates the relative potential of Cl- precursors in perchlorate production and the likely importance of dry aerosol oxidation over solution phase reactions. It also suggests that ClO2- may be a key intermediate while ClO3- and OCl- are unlikely to play a significant role

  13. Anomalous aryl strengthening of complexes at americium and europium extraction with alkylenediphospine dioxide from perchloric media

    International Nuclear Information System (INIS)

    Studied was the extraction of americium(3) and europium(3) from perchlorate solutions(0.001 M) with dioxides of alkylenediphosphines of three types: aryl Ph2P(O)CH2(O)PPh2(briefly 4P), and Ph2P(O)(CH2)2(O)PPh2, mixed Ph2P(O)CH2(O)P(C8H17)2 (or 2Ph2Oct) and alkyl (C8H17)2P(O)CH2(O)P(C8H17)2 (or 4 Oct). Trisolvates of MeS3x(ClO4)3 are predominantly formed but americium disolvates are also present upon dilution with dichloroethane. For 4Ph,2Ph2Oct and 4 Oct the concentration is, respectively, 1015, 2x1014, and 1013; for disolvates by 4 orders of magnitude lower which is, nevertheless, by 2 orders of magnitude higher than for nitric acid solutions. The separation coefficient of β Am/Eu for 4Ph attains 6-8. As in the case of nitrate solutions, an anomalous aryl strengthening of the complexes is observed: an increase in the distribution coefficients and extraction constants in the series of 4 Oct - 2Ph 2 Oct - 4Ph, in spite of the introduction of electronegative aryl substituents into the dioxide molecule, which reduce electron density on oxygen atoms and basicity of dioxides. In contrast to nitric acid solutions, observed is a nonlinear effect of a change in basicity on extraction properties upon dilution with dichloroethane (dioxide of 2Ph2 Oct does not occupy an intermediate position but is close to 4Ph). Upon dilution with chloroform the dependence is linear and anomalous effect rises due to a different nature of interactions of dioxides with chloroform. When the bridge increases up to ethylene, an anomalous strengthening of the complexes disappears. However, the distribution coefficients upon extraction with alkyl dioxide are considerably lower, which can be explained by a stronger extraction of perchloric acid

  14. Thermodynamics of the complexation of ciprofloxacin with calcium and magnesium perchlorate

    International Nuclear Information System (INIS)

    Highlights: → The thermodynamics of the reactions of ciprofloxacin (CIP) with Ca(ClO4)2 and Mg(ClO4)2 were investigated by conductometric titration. → The reactions of CIP with each ion produce two ionic complexes with the formulas M(CIP)2+ and M(CIP)22+. → The change in enthalpy and entropy were negative which indicate that the complexation is driven by the enthalpy change. - Abstract: The thermodynamics of the reactions of ciprofloxacin (CIP) with calcium perchlorate (Ca(ClO4)2) and magnesium perchlorate (Mg(ClO4)2) have been investigated in water-methanol solvent using conductometric titration. The reactions of CIP with each ion produce two ionic complexes with the general formulas M(CIP)2+ and M(CIP)22+. The stability constants K1 and K2 at 25 oC for the complexes formed from the reaction with Ca(ClO4)2 were 8.84 x 104 and 3.62 x 104, respectively. For the reaction with Mg(ClO4)2K1 and K2 were 1.72 x 105 and 2.50 x 103, respectively. The enthalpy (ΔH1, ΔH2, ΔH12) and entropy (ΔS1, ΔS2, ΔS12) of complexation reactions were determined from the temperature dependence of the complexation constants. The reactions of CIP with both ions are accompanied by a decrease in entropy (ΔS12 = -468.12 and -478.89 J/K mol for complexation with Ca(ClO4)2 and Mg(ClO4)2, respectively) and enthalpy (ΔH12 = -193.09 and -192.01 kJ/mol for complexation with Ca(ClO4)2 and Mg(ClO4)2, respectively), which indicate that the reactions are driven by the enthalpy change.

  15. Thermodynamics of the complexation of ciprofloxacin with calcium and magnesium perchlorate

    Energy Technology Data Exchange (ETDEWEB)

    Al-Mustafa, Jamil, E-mail: malkawi@just.edu.jo [Department of Applied Chemistry, Faculty of Arts and Sciences, Jordan University of Science and Technology, P.O. Box 3030, Irbid (Jordan); Taha, Ziyad A. [Department of Applied Chemistry, Faculty of Arts and Sciences, Jordan University of Science and Technology, P.O. Box 3030, Irbid (Jordan)

    2011-07-10

    Highlights: {yields} The thermodynamics of the reactions of ciprofloxacin (CIP) with Ca(ClO{sub 4}){sub 2} and Mg(ClO{sub 4}){sub 2} were investigated by conductometric titration. {yields} The reactions of CIP with each ion produce two ionic complexes with the formulas M(CIP){sup 2+} and M(CIP){sub 2}{sup 2+}. {yields} The change in enthalpy and entropy were negative which indicate that the complexation is driven by the enthalpy change. - Abstract: The thermodynamics of the reactions of ciprofloxacin (CIP) with calcium perchlorate (Ca(ClO{sub 4}){sub 2}) and magnesium perchlorate (Mg(ClO{sub 4}){sub 2}) have been investigated in water-methanol solvent using conductometric titration. The reactions of CIP with each ion produce two ionic complexes with the general formulas M(CIP){sup 2+} and M(CIP){sub 2}{sup 2+}. The stability constants K{sub 1} and K{sub 2} at 25 {sup o}C for the complexes formed from the reaction with Ca(ClO{sub 4}){sub 2} were 8.84 x 10{sup 4} and 3.62 x 10{sup 4}, respectively. For the reaction with Mg(ClO{sub 4}){sub 2}K{sub 1} and K{sub 2} were 1.72 x 10{sup 5} and 2.50 x 10{sup 3}, respectively. The enthalpy ({Delta}H{sub 1}, {Delta}H{sub 2}, {Delta}H{sub 12}) and entropy ({Delta}S{sub 1}, {Delta}S{sub 2}, {Delta}S{sub 12}) of complexation reactions were determined from the temperature dependence of the complexation constants. The reactions of CIP with both ions are accompanied by a decrease in entropy ({Delta}S{sub 12} = -468.12 and -478.89 J/K mol for complexation with Ca(ClO{sub 4}){sub 2} and Mg(ClO{sub 4}){sub 2}, respectively) and enthalpy ({Delta}H{sub 12} = -193.09 and -192.01 kJ/mol for complexation with Ca(ClO{sub 4}){sub 2} and Mg(ClO{sub 4}){sub 2}, respectively), which indicate that the reactions are driven by the enthalpy change.

  16. Biosorption of Chromium (VI) from Aqueous Solutions onto Fungal Biomass

    OpenAIRE

    Ismael Acosta R.; Xöchitl Rodríguez; Conrado Gutiérrez; Ma. de Guadalupe Moctezuma

    2004-01-01

    The biosorption of chromium (VI) on eighteen different natural biosorbents: Natural sediment, chitosan, chitin, Aspergillus flavus I-V, Aspergillus fumigatus I-ll, Helmintosporium sp, Cladosporium sp, Mucor rouxii mutant, M. rouxii IM-80, Mucor sp-I and 2, Candida albicans and Cryptococcus neoformans was studied in this work. It was found that the biomass of C. neoformans, natural sediment, Helmintosporium sp and chitosan was more efficient to remove chromium (VI) (determined spectrophotometr...

  17. Stainless Steel Leaches Nickel and Chromium into Foods During Cooking

    OpenAIRE

    Kamerud, Kristin L.; Hobbie, Kevin A.; Anderson, Kim A.

    2013-01-01

    Toxicological studies show that oral doses of nickel and chromium can cause cutaneous adverse reactions such as dermatitis. Additional dietary sources, such as leaching from stainless steel cookware during food preparation, are not well characterized. This study examined stainless steel grades, cooking time, repetitive cooking cycles, and multiple types of tomato sauces for their effects on nickel and chromium leaching. Trials included three types of stainless steels and a stainless steel sau...

  18. Genetic Predisposition for Dermal Problems in Hexavalent Chromium Exposed Population

    OpenAIRE

    Priti Sharma; Vipin Bihari; Agarwal, Sudhir K.; Goel, Sudhir K.

    2012-01-01

    We studied the effect of genetic susceptibility on hexavalent chromium induced dermal adversities. The health status of population was examined from the areas of Kanpur (India) having the elevated hexavalent chromium levels in groundwater. Blood samples were collected for DNA isolation to conduct polymorphic determination of genes, namely: NQO1 (C609T), hOGG1 (C1245G), GSTT1, and GSTM1 (deletion). Symptomatic exposed subjects (n = 38) were compared with asymptomatic exposed subjects (n = 108)...

  19. Chromium (V) compounds as cathode material in electrochemical power sources

    Science.gov (United States)

    Delnick, F.M.; Guidotti, R.A.; McCarthy, D.K.

    A cathode for use in a thermal battery, comprising a chromium (V) compound. The preferred materials for this use are Ca/sub 5/(CrO/sub 4/)/sub 3/Cl, Ca/sub 5/(CrO/sub 4/)OH, and Cr/sub 2/O/sub 5/. The chromium (V) compound can be employed as a cathode material in ambient temperature batteries when blended with a suitably conductive filler, preferably carbon black.

  20. SCIENCE AND TECHNOLOGY ACTIVITIES FOR CHROMIUM IN THE 100 AREAS

    Energy Technology Data Exchange (ETDEWEB)

    PETERSEN SW

    2009-07-02

    {sm_bullet} Primary Objective: Protect the Columbia River - Focus is control and treatment of contamination at or near the shoreline, which is influenced by bank storage {sm_bullet} Secondary Objective: Reduce hexavalent chromium to <48 parts per billion (ppb) in aquifer (drinking water standard) - Large plumes with isolated areas of high chromium concentrations (> 40,000 ppb), - Unknown source location(s); probably originating in reactor operation areas

  1. DANGER OF HEXAVALENT CHROMIUM AND STRATEGY FOR THE REMEDITATION

    OpenAIRE

    Aniruddha Roy; Ayan Das; Nirmal Paul

    2013-01-01

    Some metals as micronutrients have a major role in the life and growth process of plants and animals. However, certain forms of some metals may also act as toxic material even in relatively small quantities. Chromium is such a metal, whose concentration above a certain limit may cause a serious problem to the health of living organisms. Chromium (Cr) may occur in several chemical forms in organic and inorganic systems. In biological systems only Cr (III) and Cr (VI) are signifi...

  2. Stereology of carbide phase in modified hypereutectic chromium cast iron

    Directory of Open Access Journals (Sweden)

    J. Suchoń

    2010-04-01

    Full Text Available In paper are presented results of studies of carbide phase stereology modified hypereutectic wear resistance chromium cast iron which contains carbon about 3,5% and chromium about 25%. Three substances were applied to the modification: boron carbide (B4C, ferroniobium (FeNb and mixture of ferroniobium and rare-earth (RE. The measurements of geometrical features of carbides were conducted on microsection taken from castings wich were cooled with various velocities.

  3. Stereology of carbide phase in modified hypereutectic chromium cast iron

    OpenAIRE

    J. Suchoń; A. Studnicki; M. Przybył

    2010-01-01

    In paper are presented results of studies of carbide phase stereology modified hypereutectic wear resistance chromium cast iron which contains carbon about 3,5% and chromium about 25%. Three substances were applied to the modification: boron carbide (B4C), ferroniobium (FeNb) and mixture of ferroniobium and rare-earth (RE). The measurements of geometrical features of carbides were conducted on microsection taken from castings wich were cooled with various velocities.

  4. Chromium reduction from slag on electromelting of stainless steel

    International Nuclear Information System (INIS)

    Specific features of chromium reduction from the slag on electromelting of stainless steel type Kh18N10T according to one- or two-slag procedure were studied. It was shown that one-slag melting technology allows double decrease of chromium losses in the form of incompletely reduced oxides. This occurs due to additional chemical reactions between metal and slag on their combined pouring into the ladle. 1 ref.; 3 figs

  5. 40 CFR Appendix Xii to Part 266 - Nickel or Chromium-Bearing Materials that may be Processed in Exempt Nickel-Chromium Recovery...

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 26 2010-07-01 2010-07-01 false Nickel or Chromium-Bearing Materials that may be Processed in Exempt Nickel-Chromium Recovery Furnaces XII Appendix XII to Part 266... FACILITIES Pt. 266, App. XII Appendix XII to Part 266—Nickel or Chromium-Bearing Materials that may...

  6. Immunological detection of small organic molecules in the presence of perchlorates: relevance to the life marker chip and life detection on Mars.

    Science.gov (United States)

    Rix, Catherine S; Sims, Mark R; Cullen, David C

    2011-11-01

    The proposed ExoMars mission, due to launch in 2018, aims to look for evidence of extant and extinct life in martian rocks and regolith. Previous attempts to detect organic molecules of biological or abiotic origin on Mars have been unsuccessful, which may be attributable to destruction of these molecules by perchlorate salts during pyrolysis sample extraction techniques. Organic molecules can also be extracted and measured with solvent-based systems. The ExoMars payload includes the Life Marker Chip (LMC) instrument, capable of detecting biomarker molecules of extant and extinct Earth-like life in liquid extracts of martian samples with an antibody microarray assay. The aim of the work reported here was to investigate whether the presence of perchlorate salts, at levels similar to those at the NASA Phoenix landing site, would compromise the LMC extraction and detection method. To test this, we implemented an LMC-representative sample extraction process with an LMC-representative antibody assay and used these to extract and analyze a model sample that consisted of a Mars analog sample matrix (JSC Mars-1) spiked with a representative organic molecular target (pyrene, an example of abiotic meteoritic infall targets) in the presence of perchlorate salts. We found no significant change in immunoassay function when using pyrene standards with added perchlorate salts. When model samples spiked with perchlorate salts were subjected to an LMC-representative liquid extraction, immunoassays functioned in a liquid extract and detected extracted pyrene. For the same model sample matrix without perchlorate salts, we observed anomalous assay signals that coincided with yellow coloration of the extracts. This unexpected observation is being studied further. This initial study indicates that the presence of perchlorate salts, at levels similar to those detected at the NASA Phoenix landing site, is unlikely to prevent the LMC from extracting and detecting organic molecules from

  7. Multi-fractal property of perchlorate reductase gene sequences and DNA photonics application to UV fluorescence detection on Mars-like surfaces

    Science.gov (United States)

    Tremberger, George, Jr.; Cheung, Eric; Gadura, N.; Holden, Todd; Subramaniam, Raji; Sullivan, Regina; Schneider, Pat; Flamholz, Alex; Lieberman, David H.; Cheung, Tak D.

    2009-08-01

    The discovery of perchlorate on Mars raises the possibility of the existence of perchlorate reduction microbes on that planet. The perchlorate reductase gene sequence fractal dimensions of two Dechloromonas species were compared with five other sequences in the microbial dimethyl sulfoxide (DMSO) reductase family. A nucleotide sequence can be expressed as a numerical sequence where each nucleotide is assigned its proton number. The resulting numerical sequence can be investigated for its fractal dimension in terms of evolution and chemical properties for comparative studies. Analysis of the fractal dimensions for the DMSO reductase family supports phylogenetic analyses that show that the perchlorate reductase gene sequences are members of the same family. A sub-family with roughly the same nucleotide length emerges having the property that the gene fractal dimension is negatively correlated with the Shannon di-nucleotide entropy (R2 ~ 0.95, N =5). The gene sequence fractal dimension is found to be positively correlated with the neighbor joining distances reported in a published protein phylogeny tree (R2~ 0.92, N = 5). The multi-fractal property associated with these genes shows that perchlorate reductase has lower dimensionality as compared to the relatively higher dimensionality DNA-break repair genes Rec-A and Rad-A observed in the Dechloromonas aromatica and Deinococcus radiodurans genomes. The studied perchlorate gene sequences show a higher Shannon di-nucleotide entropy (~3.97 bits) relative to Dechloromonas aromatica DNA repair sequences (~3.87 bits Rec-A, ~3.92 bits Rad-A), suggesting that there are fewer constraints on nucleotide variety in the perchorlate sequences . These observations thus allow for the existence of perchlorate reducing microbes on Mars now or in the past. Timeresolved UV fluorescence study near the emission bands of nucleotide sequences could be used for bio-detection on Mars-like surfaces and the results may further constrain the

  8. Evaluating trivalent chromium toxicity on wild terrestrial and wetland plants.

    Science.gov (United States)

    Lukina, A O; Boutin, C; Rowland, O; Carpenter, D J

    2016-11-01

    Elevated chromium levels in soil from mining can impact the environment, including plants. Mining of chromium is concentrated in South Africa, several Asian countries, and potentially in Northern Ontario, Canada, raising concerns since chromium toxicity to wild plants is poorly understood. In the first experiment, concentration-response tests were conducted to evaluate effects of chromium on terrestrial and wetland plants. Following established guidelines using artificial soil, seeds of 32 species were exposed to chromium (Cr(3+)) at concentrations simulating contamination (0-1000 mg kg(-1)). This study found that low levels of chromium (250 mg kg(-1)) adversely affected the germination of 22% of species (33% of all families), while higher levels (500 and 1000 mg kg(-1)) affected 69% and 94% of species, respectively, from 89% of the families. Secondly, effects on seedbanks were studied using soil collected in Northern Ontario and exposed to Cr(3+) at equivalent concentrations (0-1000 mg kg(-1)). Effects were less severe in the seedbank study with significant differences only observed at 1000 mg kg(-1). Seeds exposed to Cr(3+) during stratification were greatly affected. Seed size was a contributing factor as was possibly the seed coat barrier. This study represents an initial step in understanding Cr(3+) toxicity on wild plants and could form the basis for future risk assessments. PMID:27543852

  9. Wear resistance of chromium cast iron – research and application

    Directory of Open Access Journals (Sweden)

    A. Studnicki

    2006-04-01

    Full Text Available Purpose: A short characteristic of wear resistance chromium cast iron has been presented as well as possibilities of this material researches realization in Foundry Department have been discussed.Design/methodology/approach: Main attention was given on research process of crystallization and analysis of chromium cast iron microstructure and its resistance on erosion wears. Separate part of paper was devoted to discuss the bimetallic castings with chromium cast iron layer as well as typical applications of chromium cast iron castings in minig, proccesing, metallurgical and power industry.Findings: The new method of crystallization process research with three testers (DTA-K3 was found in the work. The method makes possible to characterize sensitivity of chromium cast iron on cooling kinetic.Research limitations/implications: DTA-K3 method can be used for research of crystallization proccess of cast materials particularly for abrasion-resisting alloy.Practical implications: Wide scope researches of chromium cast iron in Foundry Department enable extending applications its material in many industries.Originality/value: Value of the paper is the presentation of researches possibilities which undertaken in Foundry Department within the range of wear resistant materials.

  10. cis-Difluoridobis(1,10-phenanthrolinechromium(III perchlorate monohydrate

    Directory of Open Access Journals (Sweden)

    Högni Weihe

    2008-02-01

    Full Text Available The title complex, [CrF2(C12H8N22]ClO4·H2O, displays a slightly distorted octahedral coordination geometry around the central chromium(III ion. The Cr environment is composed of a cis arrangement of two 1,10-phenanthroline [average CrIII—N = 2.0726 (10 Å] and two fluoride [average CrIII—F = 1.8533 (6 Å] ligands. The water molecule forms a hydrogen bond to fluorine in a neighbouring cation.

  11. Experimental skin deposition of chromium on the hands following handling of samples of leather and metal

    DEFF Research Database (Denmark)

    Bregnbak, David; Thyssen, Jacob P.; Jellesen, Morten Stendahl;

    2016-01-01

    Background: Chromium is an important skin sensitizer. Exposure to it has been regulated in cement, and recently in leather. Studies on the deposition of chromium ions on the skin as a result of handling different chromium-containing materials are sparse, but could improve the risk assessment of...... contact sensitization and allergic contact dermatitis caused by chromium. Objectives: To determine whether the handling of chromium-containing samples of leather and metal results in the deposition of chromium onto the skin. Methods: Five healthy volunteers participated. For 30 min, they handled samples...... of leather and metal known to contain and release chromium. Skin deposition of chromium was assessed with the acid wipe sampling technique. Results: Acid wipe sampling of the participants' fingers showed chromium deposition on the skin in all participants who had been exposed to leather (range 0...

  12. Effect of recasting on the thickness of metal-ceramic interface of nickel-chromium and cobalt-chromium alloys

    OpenAIRE

    Mirković Nemanja; Draganjac Miroslav; Stamenković Dragoslav; Ristić Ljubiša

    2008-01-01

    Introduction/Aim. This research was done to establish recasting effects of nickel-chromium and cobalt-chromium alloys on the thickness of their metal-ceramic interface in making fixed partial dentures. Metal-ceramic interface determines their functional integrity and prevents damages on ceramics during mastication. Investigation of metal-ceramic samples is supposed to show if base metal alloys for metalceramics are successfully recycled without any risk of reduction of metal-ceramic interface...

  13. Activation of bentonite to remove the chromium from waste water produced by panning industry, and studying the chromium recovery efficiency

    International Nuclear Information System (INIS)

    The fast development of tanning industry led to an increase in environmental problems resulting from discharging its wastes to the surrounding environment. Thus solving this problem became one of the most important aims that the researchers work on. The chromium content of the industrial water wastes of the tanning industry considered as the main pollutant for the environment. The Aleppo Bentonite is used in early research to remove the chromium from the industrial waste water.The current research aims to find a method to activate the Aleppo Bentonite in order to increase the effective removal of chromium from the industrial waste water which is produced by tanning industry, as well as to specify the optimal conditions for chromium recovery.This study used the Aleppo Bentonite, whose origin is Tal Ajar-Aleppo to study the activation aspects using Sulfuric Acid, Hydrochloric Acid and Nitric Acid, in addition to study the recovery aspects using the same acids and hydrogen peroxide and to specify the optimal conditions for chromium recovery through applying some experiments based on three main factors: concentration, settling time and temperature.It was observed from the applied experiments that it is possible to recover chromium from Bentonite efficiently up to (80% - 90%) by treating the Bentonite with hydrogen peroxide(33% concentration) at room temperature, or by treating it with hydrogen peroxide(8.25% concentration) at 75oC, while the settling time factor proved that full recovery of chromium is obtained during the first hour, and increasing the time factor does not affect the efficiency of chromium recovery. (author)

  14. Size and Shape of Ammonium Perchlorate and their Influence on Properties of Composite Propellant

    Directory of Open Access Journals (Sweden)

    Sunil Jain

    2009-05-01

    Full Text Available Most of the composite propellant compositions contain solid loading up to 86 per cent. The main solid ingredients of composite propellant are ammonium perchlorate (AP and aluminium powder. Therefore, it is a must to characterise these to improve processibility and quality of composite propellant. Effect of particle size on propellants slurry viscosity and ballistic parameters are well documented, however, the effect of oxidizer particle shape is not reported. In the present study, different methods for size and shape characterisation are discussed and effect of size and shape of AP on composite propellant properties are studied. The data indicate that as size of AP decreases, propellant slurry viscosity increases and burn rate increases. The particles having higher shape factor provides less endof mix (EOM viscosity of propellant slurry and burn rate. Further, effect of size of ground AP on shape is also investigated. From the data thus obtained, it is inferred that as size of ground AP decreases, shape factor decreases, and particles become more irregular in shape.Defence Science Journal, 2009, 59(3, pp.294-299, DOI:http://dx.doi.org/10.14429/dsj.59.1523

  15. Structure and properties of 2-cyanopyridinium perchlorate [2-CNPyH][ClO{sub 4}

    Energy Technology Data Exchange (ETDEWEB)

    Czupinski, O [Faculty of Chemistry, University of Wroclaw, Joliot-Curie 14, 50-383 Wroclaw (Poland); Wojtas, M [Faculty of Chemistry, University of Wroclaw, Joliot-Curie 14, 50-383 Wroclaw (Poland); Zaleski, J [Institute of Chemistry, University of Opole, Oleska 48, 45-951 Opole (Poland); Jakubas, R [Faculty of Chemistry, University of Wroclaw, Joliot-Curie 14, 50-383 Wroclaw (Poland); Medycki, W [Institute of Molecular Physics, Polish Academy of Science, Smoluchowskiego 17, 60-179 Poznan (Poland)

    2006-03-29

    The crystal structure of 2-cyanopyridinium perchlorate, [2-CNPyH][ClO{sub 4}], has been determined at 100 (phase II) and 293 K (phase I). It is monoclinic P 2{sub 1} at 100 K and orthorhombic P 2{sub 1}2{sub 1}2{sub 1} at 293 K. The dynamic properties of the crystal were studied by differential scanning calorimetry, dilatometry, pyroelectric, dielectric, proton ({sup 1}H NMR), chlorine ({sup 35}Cl NMR) magnetic resonance spectroscopies and the infrared method. The crystal undergoes a structural phase transition (I {yields}II) at 170K characterized by a complex mechanism involving both 'order-disorder' and 'displacive' contributions. It reveals pyroelectric properties below 170K. The dielectric relaxation existing over phase I is due to the motion of the cyano group, whereas the dynamics of the [ClO{sub 4}]{sup -} anions is reflected in the significant dielectric increment around the I {yields}II phase transition.

  16. Shock wave response of ammonium perchlorate single crystals to 6 GPa

    International Nuclear Information System (INIS)

    Plane shock wave experiments were carried out on ammonium perchlorate single crystals compressed along [210] and [001] orientations to peak stresses ranging from 1.2 to 6.2 GPa. Quartz gauge and velocity interferometer techniques were used to measure the elastic and plastic shock wave velocities, and stress and particle velocity histories in the shocked samples. The measured Hugoniot elastic limit (HEL) was 0.48±0.09 GPa. Above the HEL and up to about 6 GPa, the data show a clear two-wave structure, indicating an elastic-plastic response. Time-dependent elastic precursor decay and plastic wave ramping are discernable and orientation dependent in the low stress data. However, the orientation dependence of the peak state response is small. Hence, data for both orientations were summarized into a single isotropic, elastic-plastic-stress relaxation model. Reasonable agreement was obtained between the numerical simulations using this model and the measured wave profiles. At a shock stress of about 6 GPa and for the time duration and crystal orientations examined, we did not observe any features that may be identified as a sustained chemical reaction or a phase transformation. (c) 2000 American Institute of Physics

  17. Microscopic observations of X-ray and gamma-ray induced decomposition of ammonium perchlorate crystals

    Science.gov (United States)

    Herley, P. J.; Levy, P. W.

    1972-01-01

    The X-ray and gamma-ray induced decomposition of ammonium perchlorate was studied by optical, transmission, and scanning electron microscopy. This material is a commonly used oxidizer in solid propellents which could be employed in deep-space probes, and where they will be subjected to a variety of radiations for as long as ten years. In some respects the radiation-induced damage closely resembles the effects produced by thermal decomposition, but in other respects the results differ markedly. Similar radiation and thermal effects include the following: (1) irregular or ill-defined circular etch pits are formed in both cases; (2) approximately the same size pits are produced; (3) the pit density is similar; (4) the c face is considerably more reactive than the m face; and (5) most importantly, many of the etch pits are aligned in crystallographic directions which are the same for thermal or radiolytic decomposition. Thus, dislocations play an important role in the radiolytic decomposition process.

  18. Spectroscopic and structural studies of di-ureasils doped with lithium perchlorate

    International Nuclear Information System (INIS)

    Di-urea cross-linked POE/siloxane hybrid ormolytes (di-ureasils) doped with a wide concentration range of lithium perchlorate trihydrate (LiClO4.3H2O) (200 ≥ n ≥ 0.5, where n expresses the salt content in terms of the number of ether oxygen atoms per Li+ ion) have been analysed by Fourier transform infrared and Raman (FT-IR and FT-Raman, respectively) spectroscopies and X-ray diffraction (XRD). The results obtained lead us to conclude that the xerogels with n ≥ 5 are totally amorphous. At n ≤ 1 free salt is observed. 'Free' ClO4- ions appear to be the main charge carriers at the conductivity maximum located within the 25 ≤ n ≤ 8 composition range of this family of ormolytes. At n = 15 ClO4- ions coordinated in mono/tridentate (C3v symmetry) and bidentate (C2v symmetry) configurations were detected. In salt-rich samples with n + ions bond to the urea carbonyl oxygen atoms over the entire range of salt concentration studied

  19. Ion Conduction and Polymer Dynamics of Poly(2-vinylpyridine) - Lithium Perchlorate Mixtures

    Science.gov (United States)

    Atorngitjawat, Pornpen; Runt, James

    2008-03-01

    Ion conduction and polymer dynamics of single phase mixtures of poly(2-vinylpyridine) (P2VPy) with 0.1 to 10 mol% lithium perchlorate (LiClO4) were investigated using broadband dielectric spectroscopy. Interpretation of the relaxation behavior was assisted by findings from wide-angle and small-angle X-ray scattering experiments, and other techniques. Five dielectric relaxations were observed: a local β process in the glassy state, a segmental relaxation, a slow segmental process, an ion-mode relaxation, and electrode polarization. The local P2VPy relaxation was strongly suppressed with increasing LiClO4 content arising from the formation of transient crosslinks, which lead to a subsequent decrease in the number of free pyridine groups, and/or a reduction in the local free volume in the presence of LiClO4. Ion conduction at low LiClO4 concentrations (diffusion of anions through the matrix, which is strongly coupled with the segmental relaxation. At relatively high LiClO4 concentration (10 mol%), partial decoupling between ion motion and the segmental relaxation was observed, leading to increased conductivity.

  20. Effect of Surface Microstructure on the Temperature sensitivity of Burning Rate of Ammonium Perchlorate

    Directory of Open Access Journals (Sweden)

    K. Kishore

    1997-04-01

    Full Text Available Considering Vielle's law and the new thermodynamic model which the authors have developed recently the true dependence of temperature sensitivity of burning rate of ammonium perchlorate (AP on pressure is resolved and experimentally verified for bellet burning. The value of decreases with pressure steeply in regime I' (below 20 atm, but gently in regime I (above 20 atm. The value of powder AP has been determined and it is observed that (powder > (pellet, which clearly suggests that of is innuenced by the surface temperature sensitive parameter and hence by the surface/subsurface microstructure. In powder burning, the buoyant lifting of the particles into the gas phase occurs, Which constitutes the so-called 'free board region' (FER extending just above the true surface. Consequent to the decomposition of AP particles in FER, the condensed phase heat release gets curtailed and (powder becomes larger. A general relationship for in terms of density and surface temperature is suggested, which is applicable to both pellet and powder AP.

  1. Stoichiometric analysis of ammonium nitrate and ammonium perchlorate with nanosecond laser induced breakdown spectroscopy

    Science.gov (United States)

    Sreedhar, S.; Rao, S. Venugopal; Kiran, P. Prem; Tewari, Surya P.; Kumar, G. Manoj

    2010-04-01

    We present our results on the stoichiometric analysis of ammonium nitrate (AN) and ammonium Perchlorate (AP) studied using laser induced breakdown spectroscopy (LIBS) with nanosecond pulses. The LIBS spectra collected for AP and AN, without any gating and using a high resolution spectrometer, exhibited characteristic lines corresponding to O, N, H, C, and K. The Oxygen line at 777.38 nm and three Nitrogen lines (N1, N2, N3) at 742.54 nm, 744.64 nm, 747.12 nm were used for evaluating the Oxygen/Nitrogen ratios. The intensities were calculated using area under the peaks and normalized to their respective transition probabilities and statistical weights. The O/N1 ratios estimated from the LIBS spectra were ~4.94 and ~5.11 for AP and O/N3 ratios were ~1.64 and ~1.47 for AN obtained from two independent measurements. The intensity ratios show good agreement with the actual stoichiometric ratios - four for AP and one for AN.

  2. Poly[[μ2-acetato-aquadi-μ3-isonicotinato-holmium(IIIsilver(I] perchlorate

    Directory of Open Access Journals (Sweden)

    Sun Feng

    2009-12-01

    Full Text Available In the title three-dimensional heterometallic complex, {[AgHo(C6H4NO22(C2H3O2(H2O]ClO4}n, the HoIII ion is eight-coordinated by four O atoms from four different isonicotinate ligands, three O atoms from two different acetate ligands and one O atom of a water molecule. The two-coordinate AgI ion is bonded to two N atoms from two different isonicotinate anions. These metal coordination units are connected by bridging isonicotinate and acetate ligands, generating a three-dimensional network. The coordinated water molecules link the carboxylate group of the acetate ligand and the nitrate ligand by O—H...O hydrogen bonding. The crystal structure is further stabilized by hydrogen bonds. The perchlorate ion is disordered over two sites with site-occupancy factors 0.539 (12 and 0.461 (12, while the methyl group of the acetate ligand is disordered over two sites with site-occupancy factors 0.51 (4 and 0.49 (4.

  3. Potentiometric anion selectivity of polymer-membrane electrodes based on cobalt, chromium, and aluminum salens

    Energy Technology Data Exchange (ETDEWEB)

    Badr, Ibrahim H.A. [Department of Chemistry, Faculty of Science, Ain Shams University, P.O. Box 11566, Cairo (Egypt)]. E-mail: ibadr1@yahoo.com

    2006-06-16

    Metallo-salens of cobalt(II) (Co-Sal), chromium(III) (Cr-Sal), and aluminum(III) (Al-Sal) are used as the active ionophores within plasticized poly(vinyl chloride) membranes. It is shown that central metal-ion plays a critical role in directing the ionophore selectivity. Polymer-membrane electrodes based on Co-Sal, Cr-Sal, and Al-Sal are demonstrated to exhibit enhanced responses and selectivity toward nitrite/thiocyanate, thiocyanate, and fluoride anions, respectively. The improved anion selectivity of the three ionophore systems is shown to deviate significantly from the classical Hofmeister pattern that is based only on ion lipophilicity. For example, optimized membrane electrodes for nitrite ion based on Co-Sal exhibit logK{sub Nitrite,Anion}{sup pot} values of -5.22, -4.66, -4.48, -2.5 towards bromide, perchlorate, nitrate, and iodide anions, respectively. Optimized membrane electrodes based on Co-Sal and Cr-Sal show near-Nernstian responses towards nitrite (-57.9+/-0.9mV/decade) and thiocyanate (-56.9+/-0.8mV/decade), respectively, with fast response and recovery times. In contrast, Al-Sal based membrane electrodes respond to fluoride ion in a super-Nernstian (-70+/-3mV/decade) and nearly an irreversible mode. The operative response mechanism of Co-Sal, Cr-Sal, and Al-Sal membrane electrodes is examined using the effect of added ionic sites on the potentiometric response characteristics. It is demonstrated that addition of lipophilic anionic sites to membrane electrodes based on the utilized metallo-salens enhances the selectivity towards the primary ion, while addition of cationic sites resulted in Hofmeister selectivity patterns suggesting that the operative response mechanism is of the charged carrier type. Electron spin resonance (ESR) data indicates that Co(II) metal-ion center of Co-Sal ionophore undergoes oxidation to Co(III). This process leads to formation of a charged anion-carrier that is consistent with the response behavior obtained for Co

  4. Scientific Opinion on chromium(III) lactate tri-hydrate as a source of chromium added for nutritional purposes to foodstuff

    OpenAIRE

    EFSA Panel on Food Additives and Nutrient Sources added to Food (ANS)

    2012-01-01

    The Panel on Food Additives and Nutrient Sources added to Food provides a scientific opinion on the safety and bioavailability of chromium(III) lactate tri-hydrate as a source of chromium(III) added for nutritional purposes to foodstuffs. The safety of chromium itself, in terms of the amounts that may be consumed, is outside the remit of this Panel. No new data have been provided as regards the safety and bioavailability of chromium from chromium(III) lactate tri-hydrate. The Panel c...

  5. Creep deformation of TD--nickel chromium

    International Nuclear Information System (INIS)

    The creep behavior of thoria dispersed nickel-chromium (TD-NiCr) was examined at 10930C. Major emphasis was placed on 1) the effects of the material and the test related variables (grain size, temperature, stress, strain and strain rate) on the deformation characteristics, and 2) the evaluation of single crystal TD-NiCr material produced by a directional recrystallization technique. Creep activation enthalpies were found to increase with increasing grain size reaching maximum values for the single crystal TD-NiCr. Stress exponent of the steady state creep rate was also significantly higher for the single crystal material as compared with that determined for the polycrystalline TD-NiCr. The elevated temperature deformation of TD-NiCr was analyzed in terms of two parallel-concurrent processes: 1) diffusion controlled grain boundary sliding and 2) dislocation motion. The characteristics of the dislocation motion deformation mode (as observed in the single crystal TD-NiCr) suggest that strong particle-dislocation interactions are present. The relative contributions of dislocation motion and grain boundary sliding in TD-NiCr were estimated. In creep, grain boundary sliding was found to predominate for the small, equiaxed grain structures, whereas the dislocation deformation mode became significant for only the large grain TD-NiCr and the single crystal material

  6. Low energy spin excitations in chromium metal

    Energy Technology Data Exchange (ETDEWEB)

    Pynn, R. [Los Alamos National Lab., NM (United States); Azuah, R.T. [Hahn-Meitner-Inst., Berlin (Germany); Stirling, W.G. [Univ. of Liverpool (United Kingdom). Dept. of Physics; Kulda, J. [Inst. Laue Langevin, Grenoble (France)

    1997-12-31

    Neutron scattering experiments with full polarization analysis have been performed with a single crystal of chromium to study the low-energy spin fluctuations in the transverse spin density wave (TSDW) state. A number of remarkable results have been found. Inelastic scattering observed close to the TSDW satellite positions at (1 {+-} {delta},0,0) does not behave as expected for magnon scattering. In particular, the scattering corresponds to almost equally strong magnetization fluctuations both parallel and perpendicular to the ordered moments of the TSDW phase. As the Neel temperature is approached from below, scattering at the commensurate wavevector (1,0,0) increases in intensity as a result of critical scattering at silent satellites (1,0, {+-} {delta}) being included within the spectrometer resolution function. This effect, first observed by Sternlieb et al, does not account for all of the inelastic scattering around the (1,0,0) position, however, Rather, there are further collective excitations, apparently emanating from the TSDW satellites, which correspond to magnetic fluctuations parallel to the ordered TSDW moments. These branches have a group velocity that is close to that of (1,0,0) longitudinal acoustic (LA) phonons, but assigning their origin to magneto-elastic scattering raises other unanswered questions.

  7. A Rare Terminal Dinitrogen Complex of Chromium

    Energy Technology Data Exchange (ETDEWEB)

    Mock, Michael T.; Chen, Shentan; Rousseau, Roger J.; O' Hagan, Molly J.; Dougherty, William G.; Kassel, W. S.; DuBois, Daniel L.; Bullock, R. Morris

    2011-10-12

    The reduction of dinitrogen to ammonia from N2 and H2 is currently carried out by the Haber-Bosch process, an energy intensive process that requires high pressures and high temperatures and accounts for the production of millions of tons of ammonia per year. The development of a catalytic, energy-efficient process for N2 reduction is of great interest and remains a formidable challenge. In this communication, we are reporting the preparation, characterization and computational electronic structure analysis of a rare 'Chatt-type' ((P-P)2M(N2)2, P-P = diphosphine ligand) complex of chromium, cis-[Cr(N2)2(PPh2NBn2)2] and its reactivity with CO. This complex is supported by the diphosphine ligand PPh2NBn2, containing non-coordinating pendant amine bases, to serve as proton relays. Future studies for this complex are aimed at answering fundamental questions regarding the role of proton relays in the second coordination sphere in their ability to facilitate proton movement from an external acid to metal-bound dinitrogen ligands in the challenging multi-proton/electron reduction of N2 to ammonia.

  8. A Rare Terminal Dinitrogen Complex of Chromium

    International Nuclear Information System (INIS)

    The reduction of dinitrogen to ammonia from N2 and H2 is currently carried out by the Haber-Bosch process, an energy intensive process that requires high pressures and high temperatures and accounts for the production of millions of tons of ammonia per year. The development of a catalytic, energy-efficient process for N2 reduction is of great interest and remains a formidable challenge. In this communication, we are reporting the preparation, characterization and computational electronic structure analysis of a rare 'Chatt-type' ((P-P)2M(N2)2, P-P = diphosphine ligand) complex of chromium, cis-(Cr(N2)2(PPh2NBn2)2) and its reactivity with CO. This complex is supported by the diphosphine ligand PPh2NBn2, containing non-coordinating pendant amine bases, to serve as proton relays. Future studies for this complex are aimed at answering fundamental questions regarding the role of proton relays in the second coordination sphere in their ability to facilitate proton movement from an external acid to metal-bound dinitrogen ligands in the challenging multi-proton/electron reduction of N2 to ammonia.

  9. Hexavalent Chromium Reduction and Its Distribution in the Cell and Medium by Chromium Resistant Fusarium solani

    Directory of Open Access Journals (Sweden)

    Mousumi Sen

    2013-01-01

    Full Text Available In the present work, batch biosorption of Cr(VI was studied using the fungal strain isolated from soil. The fungal strain was characterized as Fusarium solani. The total Cr distribution in the biomass (fungus and in the media obtained from the experiment conducted at 500 mg l -1 initial Cr(VI concentration and pH 5.0. The results indicated both intracellular and extracellular accumulation and enzymatic reduction of Cr(VI and this was supported by the Transmission Electron Microscopic (TEM observation at the same Cr(VI concentration and pH value. Chromium elution from Fusarium solani containing Cr was then tried out using a number of chromium eluting reagents and a maximum Cr could be eluted using 0.5N sodium hydroxide solution without destructing the biomass structure. The total Cr was recovered by pH adjustment from both biomass and media was found to be 44% of the initial Cr(VI concentration (500 mg l-1.

  10. Electron transfer. 75. Reduction of carboxylato-bound chromium(V) with vanadium(IV). Intervention of chromium(IV)

    International Nuclear Information System (INIS)

    The chelated (carboxylato)chromium(V) anion bis(2-hydroxy-2-ethylbutyrato)oxochromate(V) (I), [(Lig)2Cr(O)]-, reacts with oxovanadium(IV) to form a strongly absorbing species (lambda/sub max/ = 515 nm; epsilon = 1.7 x 103 M-1) in the presence of 2-hydroxy-2-ethylbutyric acid buffers (pH 2-4). EPR data support 1:1 stoichiometry with VO2+ in deficiency, indicating the formation of a chromium(IV) species by reduction. With excess VO2+ a chromium(III) product was obtained. Spectral and ion-exchange properties of this product correspond to those observed for the titanium(III) and iron(II) reductions of chromium(V) and are consistent with the formulation of the product as a bis(hydroxycarboxylate) chelate of (H2O)2Cr/sup III/. With excess vanadium(IV), the reaction exhibits triphasic kinetics. The remaining step of the reaction is the reduction of the chromium(IV) intermediate with VO2+. Rates for all steps increase with decreasing [H+] and level off at low [H+]. The limiting rate constants for the formation of the chromium(IV) intermediate by the (Lig)3Cr(O)2- and (Lig)2Cr(O)- pathways are 2.8 x 103 and 2.2 x 102 M-1s-1. The bimolecular limiting rate constant for the reduction of chromium(IV) is computed to be 7.7 x 102 M-1 s-1. 33 references, 7 tables

  11. Structural characterization, phase transition and dielectric properties of 4-cyanopyridynium perchlorate monohydrate: [(4-CNC 5H 4NH)][ClO 4]·H 2O

    Science.gov (United States)

    Czupiński, O.; Wojtaś, M.; Pietraszko, A.; Jakubas, R.

    2007-01-01

    Crystal structure of 4-cyanopyridynium perchlorate monohydrate ([(4-CNC 5H 4NH)][ClO 4]·H 2O) has been determined at 293 and 240 K as orthorhombic space group, Pnma and monoclinic space group, P2 1/ c, respectively, by means of single crystal X-ray diffraction. At room temperature the perchlorate anion reveals significant disorder, which is realized by the splitting of two oxygen atoms into four sites. DSC, dilatometric and dielectric spectroscopy techniques show that the crystal undergoes phase transition at 286/288 K (on cooling/heating scans). [(4-CNC 5H 4NH)][ClO 4]·H 2O appears to be an insulator with relatively high activation energy of the order of 100 kJ/mol. The phase transition in the title crystal is believed to be related to the dynamics of the perchlorate anion.

  12. Chromium propionate enhances adipogenic differentiation of bovine intramuscular adipocytes

    Directory of Open Access Journals (Sweden)

    Rebecca eTokach

    2015-09-01

    Full Text Available In vitro experiments were performed to determine the effects of increasing concentrations of chromium propionate on mRNA and protein abundance of different enzymes and receptors. Intramuscular and subcutaneous preadipocytes and bovine satellite cells were isolated from the longissimus muscle to determine the effect of treatment on glucose transporter type 4 (GLUT4 and peroxisome proliferator-activated receptor γ mRNA and GLUT4 protein abundance. Preadipocyte cultures were treated with differentiation media plus either sodium propionate or different concentrations of chromium propionate (CrPro for 96, 120, and 144 h before harvest. This study indicated adipogenesis of the bovine intramuscular adipocytes were more sensitive to the treatment of chromium propionate as compared to subcutaneous adipocytes. Enhancement of adenosine monophosphate-activated protein kinase and GLUT4 mRNA by CrPro treatment may enhance glucose uptake in intramuscular adipocytes. Chromium propionate decreased GLUT4 protein levels in muscle cell cultures suggesting those cells have increased efficiency of glucose uptake due to exposure to increased levels of CrPro. In contrast, each of the two adipogenic lines had opposing responses to the CrPro. It appeared that CrPro had the most stimulative effect of GLUT4 response in the intramuscular adipocytes as compared to subcutaneous adipocytes. These findings indicated opportunities to potentially augment marbling in beef cattle fed chromium propionate during the finishing phase.

  13. Anthropogenic chromium emissions in china from 1990 to 2009.

    Science.gov (United States)

    Cheng, Hongguang; Zhou, Tan; Li, Qian; Lu, Lu; Lin, Chunye

    2014-01-01

    An inventory of chromium emission into the atmosphere and water from anthropogenic activities in China was compiled for 1990 through to 2009. We estimate that the total emission of chromium to the atmosphere is about 1.92×10⁵ t. Coal and oil combustion were the two leading sources of chromium emission to the atmosphere in China, while the contribution of them showed opposite annual growth trend. In total, nearly 1.34×10⁴ t of chromium was discharged to water, mainly from six industrial categories in 20 years. Among them, the metal fabrication industry and the leather tanning sector were the dominant sources of chromium emissions, accounting for approximately 68.0% and 20.0% of the total emissions and representing increases of 15.6% and 10.3% annually, respectively. The spatial trends of Cr emissions show significant variation based on emissions from 2005 to 2009. The emission to the atmosphere was heaviest in Hebei, Shandong, Guangdong, Zhejiang and Shanxi, whose annual emissions reached more than 1000t for the high level of coal and oil consumption. In terms of emission to water, the largest contributors were Guangdong, Jiangsu, Shandong and Zhejiang, where most of the leather production and metal manufacturing occur and these four regions accounted for nearly 47.4% of the total emission to water. PMID:24505309

  14. Anthropogenic chromium emissions in china from 1990 to 2009.

    Directory of Open Access Journals (Sweden)

    Hongguang Cheng

    Full Text Available An inventory of chromium emission into the atmosphere and water from anthropogenic activities in China was compiled for 1990 through to 2009. We estimate that the total emission of chromium to the atmosphere is about 1.92×10⁵ t. Coal and oil combustion were the two leading sources of chromium emission to the atmosphere in China, while the contribution of them showed opposite annual growth trend. In total, nearly 1.34×10⁴ t of chromium was discharged to water, mainly from six industrial categories in 20 years. Among them, the metal fabrication industry and the leather tanning sector were the dominant sources of chromium emissions, accounting for approximately 68.0% and 20.0% of the total emissions and representing increases of 15.6% and 10.3% annually, respectively. The spatial trends of Cr emissions show significant variation based on emissions from 2005 to 2009. The emission to the atmosphere was heaviest in Hebei, Shandong, Guangdong, Zhejiang and Shanxi, whose annual emissions reached more than 1000t for the high level of coal and oil consumption. In terms of emission to water, the largest contributors were Guangdong, Jiangsu, Shandong and Zhejiang, where most of the leather production and metal manufacturing occur and these four regions accounted for nearly 47.4% of the total emission to water.

  15. Enhancement of chromium uptake in tanning using oxazolidine.

    Science.gov (United States)

    Sundarapandiyan, S; Brutto, Patrick E; Siddhartha, G; Ramesh, R; Ramanaiah, B; Saravanan, P; Mandal, A B

    2011-06-15

    Monocyclic and bicyclic oxazolidines were offered at three different junctures of chrome tanning process viz. prior to BCS offer, along with BCS and after basification. It was found that oxazolidine when offered after basification brought about better chromium uptake and reduction of chromium load in the wastewater. Offer of oxazolidine was also varied. Increase in offer of oxazolidine from 0.25% to 1% was found to enhance the chromium uptake and decrease the chromium load in wastewater. But the increase in uptake was not proportionate to the increase in oxazolidine offer more than 0.75%. Offer of 1% Zoldine ZA 78 (monocyclic oxazolidine) and Zoldine ZE (bicyclic oxazolidine) after basification brought about 63.4% and 73.1% enhancement in chrome content in leather compared to control where oxazolidine was not offered. The tone of the wetblue was found to be altered moderately. However this did not call for any process adjustments in wet-finishing. The oxazolidine treated leathers were found to be immensely fuller and tighter. It was found experimentally that offer of 1% of oxazolidine facilitated reduction in the offer of syntans administered for filling and grain tightening by around 46%. Oxazolidine could bring about significant reduction in cost of chemicals apart from resulting environmental benefits due to enhancement of chromium uptake during tanning. PMID:21536383

  16. Low-chromium reduced-activation ferritic steels for fusion

    Energy Technology Data Exchange (ETDEWEB)

    Klueh, R.L.; Alexander, D.J.; Kenik, E.A. [Oak Ridge National Laboratory, TN (United States)

    1996-04-01

    Development of reduced-activation ferritic steels has concentrated on high-chromium (8-10 wt% Cr) steels. However, there are advantages for a low-chromium steel, and initial ORNL studies on reduced-activation steels were on compositions with 2.25 to 12% Cr. Those studies showed an Fe-2.25Cr-2W-0.25V-0.1C (2 1/4Cr-2WV) steel to have the highest strenglth of the steels studied. Although this steel had the best strength, Charpy impact properties were inferior to those of an Fe-9Cr-2W-0.25V-0.07Ta-0.1C (9Cr-2WVTa) and an Fe-2.25Cr-2W-0.1C (2 1/4Cr-2W) steel. Therefore, further development of the low-chromium Cr-W steels was required. These results indicate that it is possible to develop low-chromium reduced-activation ferritic steels that have tensile and impact properties as good or better than those of high-chromium (7-9% Cr) steels. Further improvement of properties should be possible by optimizing the composition.

  17. Shock sensitivity of the explosive 2-(5-Cyanotetrazolato) Pentaamine Cobalt(III) Perchlorate (CP)

    International Nuclear Information System (INIS)

    The inorganic explosive, 2-(5-Cyanotetrazolato) Pentaamine Cobalt(III) Perchlorate, more commonly designated CP, is used in a number of hot-wire initiated deflagration-to-detonation detonators. Analyses of the safety aspects of these detonators are dependent upon utilizing shock initiation sensitivity data on this explosive where sensitivity is defined as the amplitude (P) and duration (tau) of the shock stimulus which produces a 50% probability of initiation. In this work the shock sensitivity of CP powder pressed to 1.50 Mg/m3 bulk density was determined using flyer plate impact techniques which provided pulse durations of 0.17 μs and 0.23 μs and pulse amplitudes of 0.8 to 2.3 GPa. Impact tests were conducted in air and vacuum, and with flyers of different area. It was necessary to develop a new test technique to generate flyer velocities to bracket the threshold of initiation for this study. This was done by electrically exploding a metal foil against a lucite shock-moderator from which a plastic flyer lifted off at a controlled velocity. The energy source was a large capacitor bank and provided flyer velocities repeatable within 7% and with a planarity of 30 ns or less. The pressure thresholds for detonation of CP were found to be 1.75 GPa and 1.40 GPa, for pulse durations of 0.17 μs and 0.23 μs respectively. There was no discernible difference in response between samples tested in air or vacuum, or with flyers of different area, within experimental error

  18. Widespread presence of naturally occurring perchlorate in high plains of Texas and New Mexico

    Science.gov (United States)

    Rajagopalan, S.; Anderson, T.A.; Fahlquist, L.; Rainwater, K.A.; Ridley, M.; Jackson, W.A.

    2006-01-01

    Perchlorate (ClO4-) occurrence in groundwater has previously been linked to industrial releases and the historic use of Chilean nitrate fertilizers. However, recently a number of occurrences have been identified for which there is no obvious anthropogenic source. Groundwater from an area of 155 000 km2 in 56 counties in northwest Texas and eastern New Mexico is impacted by the presence of ClO4-. Concentrations were generally low (<4 ppb), although some areas are impacted by concentrations up to 200 ppb. ClO4- distribution is not related to well type (public water system, domestic, agricultural, or water-table monitoring) or aquifer (Ogallala, Edward Trinity High Plains, Edwards Trinity Plateau, Seymour, or Cenozoic). Results from vertically nested wells strongly indicate a surface source. The source of ClO4- appears to most likely be atmospheric deposition. Evidence supporting this hypothesis primarily relates to the presence of ClO 4- in tritium-free older water, the lack of relation between land use and concentration distribution, the inability of potential anthropogenic sources to account for the estimated mass of ClO4-, and the positive relationship between conserved anions (e.g., IO3-, Cl-, SO4-2) and ClO4-. The ClO4- distribution appears to be mainly related to evaporative concentration and unsaturated transport. This process has led to higher ClO4- and other ion concentrations in groundwater where the water table is relatively shallow, and in areas with lower saturated thickness. Irrigation may have accelerated this process in some areas by increasing the transport of accumulated salts and by increasing the number of evaporative cycles. Results from this study highlight the potential for ClO4- to impact groundwater in arid and semiarid areas through long-term atmospheric deposition. ?? 2006 American Chemical Society.

  19. Solution-reaction Calorimetric Study of Coordination Compounds of Rare Earth Perchlorates with Alanine and Imidazole

    Institute of Scientific and Technical Information of China (English)

    ZHAO, Yan-Ru(赵艳茹); HOU, An-Xin(侯安新); DONG, Jia-Xin(董家新); ZHAO, Shun-Sheng(赵顺省); LIU, Yi(刘义); QU, Song-Sheng(屈松生)

    2004-01-01

    Two coordination compounds of rare earth perchlorates with alanine and imidazole, [RE(Ala)n(Im)(H2O)](ClO4)3(s) (RE=La, n=3; RE=Nd, n=2), have been prepared and characterized. The standard molar enthalpies of reaction for the following two reactions, LaCL·7H2O(s)+3Ala(s)+Im(s)+3NaClO4(s)=[La(Ala).(Im)(H2O)]-(ClO4)3(s)+3NaCl(s)+6H2O(I)(1)and NdCl3·6H2O(s)+2Ala(s)+2Ala(s)+Im(s)+3NaClO4(s)=[Nd(Ala)2(Im)(H2O)]-(ClO4)3(s)+3NaCl(s)+5H2O(l) (2), were determined by solution-reaction calorimetry, at T=298.15 K, as 36.168 ±0.642kJ·mol-1 and 48.590±0.934kJ·mol-1 respectively. From the results and other auxiliary quantities, the standard molar enthalpies of formation of [La(Ala)3(Im)(H2O)](ClO4)3(s) and [Nd(Ala)2(Im)(H2O)] (ClO4)3(s) were derived,△fH(-)m{[La(Ala).(Im)(H2O)](ClO4)3,s}=(-2984.8±1.0)kJ·mol-1 and △fH(-)m{[Nd(Ala).(Im)(H2O)]-(ClO4)3,s}=(-2387.8±0.8)kJ·mol-1, respectively.

  20. FORMATION AND DESTRUCTION OF HEXAVALENT CHROMIUM IN A LABORATORY SWIRL FLAME INCINERATOR

    Science.gov (United States)

    The partitioning of chromium (Cr) in combustion systems was investigated theoretically and experimentally. Theoretical predictions were based on chemical equilibrium and suggested that hexavalent chromium [Cr(VI)] was favored by the presence of chlorine (Cl) and diminished by the...

  1. 4,4,5,5-Tetramethyl-2-(4-pyridinio-2-imidazoline-1-oxyl-3-oxide perchlorate

    Directory of Open Access Journals (Sweden)

    Kai Jiang

    2009-05-01

    Full Text Available The crystal structure of the title compound, C12H17N3O2+·ClO4−, consists of 4,4,5,5-tetramethyl-2-(4-pyridinioimidazoline-1-oxyl-3-oxide radical cations and perchlorate anions. Both the cation and the Cl atom of the anion are located on the same twofold rotation axis, and the crystal structure shows the average structure for the radical cation. The five-membered ring assumes a half-chair conformation. The cation links with the anion via N—H...O hydrogen bonding.

  2. Kinetics and mechanism of oxidation of glycine by iron(III)-1,10-phenanthroline complex in perchloric acid medium

    Indian Academy of Sciences (India)

    T V N Partha Sarathi; A Kalyan Kumar; K Krishna Kishore; P Vani

    2005-07-01

    Kinetics and mechanism of oxidation of glycine by iron(III)-1,10-phenanthroline complex has been studied in perchloric acid medium. The reaction is first order with respect to iron(III) and glycine. An increase in (phenanthroline) increases the rate, while increase in [H+] decreases the rate. Hence it can be inferred that the reactive species of the substrate is the zwitterionic form and that of the oxidant is [Fe(phen)2(H2O)2]3+. The proposed mechanism leads to the rate law as elucidated.

  3. Eu(III) extraction by bis(2-ethylhexyl)phosphoric acid and 8-hydroxyquinoline in dodecane from perchlorate medium

    International Nuclear Information System (INIS)

    Europium(III) was extracted by bis(2-ethylhexyl)phosphoric acid (HDEHP) and 8-hydroxyquinoline (HQ) in dodecane from aqueous perchlorate media of constant ionic strength (0.1M; H+, NaClO4). Slope analysis of the data indicate that three molecules of HDEHP or HQ are attached to Eu3+. Extraction constants were obtained at different temperatures. The data were used to calculate the thermodynamic parameters (ΔG, ΔH and ΔS) for the extraction process in the two systems. When using mixtures of crown ethers with HDEHP no synergism was observed. (author) 18 refs.; 8 figs.; 3 tabs

  4. Thermodynamics of Eu(III) extraction by Bis (2-ethylhexyl) phosphoric acid or 8-hydroxyquinoline in dodecane from perchlorate medium

    International Nuclear Information System (INIS)

    Europium (III) was extracted by bis (2-ethylhexyl) phosphoric acid (HDEHP) and 8-hydroxyquinoline (Hq) at different temperatures in dodecane, from perchlorate aqueous media of constant ionic strength (0.1 M ; H+, NaCl O4). Slope analysis of the data indicated that three molecules of HDEHP or Hq are attached to Eu3+. The extraction constants were evaluated at different temperatures. The data obtained were used to calculate the thermodynamic parameters (Δ G,Δ H and Δ S ) for the two systems. Some trials to use mixtures of crown ethers with the reagents investigated but no synergism was observed. 8 fig.,3 tab

  5. (Per)chlorate reduction by the thermophilic bacterium Moorella perchloratireducens sp. nov., isolated from underground gas storage

    OpenAIRE

    Balk, M.; Gelder, van, M.; Weelink, S.A.B.; Stams, A.J.M.

    2008-01-01

    A thermophilic bacterium, strain An10, was isolated from underground gas storage with methanol as a substrate and perchlorate as an electron acceptor. Cells were gram-positive straight rods, 0.4 to 0.6 µm in diameter and 2 to 8 µm in length, growing as single cells or in pairs. Spores were terminal with a bulged sporangium. The temperature range for growth was 40 to 70°C, with an optimum at 55 to 60°C. The pH optimum was around 7. The salinity range for growth was between 0 and 40 g NaCl lite...

  6. (Per)chlorate Reduction by the Thermophilic Bacterium Moorella perchloratireducens sp. nov., Isolated from Underground Gas Storage▿

    OpenAIRE

    2007-01-01

    A thermophilic bacterium, strain An10, was isolated from underground gas storage with methanol as a substrate and perchlorate as an electron acceptor. Cells were gram-positive straight rods, 0.4 to 0.6 μm in diameter and 2 to 8 μm in length, growing as single cells or in pairs. Spores were terminal with a bulged sporangium. The temperature range for growth was 40 to 70°C, with an optimum at 55 to 60°C. The pH optimum was around 7. The salinity range for growth was between 0 and 40 g NaCl lite...

  7. Preignition reactions of AP-HTPB propellants studied by IR spectrometry. [Ammonium Perchlorate-Hydroxyl Terminated PolyButadiene

    Science.gov (United States)

    Law, R. J.; Baer, A. D.; Ryan, N. W.

    1977-01-01

    IR absorption spectrometry was used to follow the disappearance of NH and CH bonds during the pyrolysis of a polymer film containing 30 weight percent ammonium perchlorate (AP). The remaining 70 weight percent consisted of a mixture of 92.5 weight percent hydroxyl-terminated polybutadiene (HTPB) and 7.5 weight percent isophrone diisocyanate (IPDI). The results indicate that polymer decomposition is induced by products of AP decomposition, and that about 2.5 CH bonds disappear for each NH bond that disappears. The diffusion process occurring in the later stages of the reaction is analyzed in an attempt to account for the unexpectedly low activation energy.

  8. On the adhesion between hydroxyl-terminated polybutadiene fuel-binder and ammonium perchlorate. Performance of bonding agents

    Energy Technology Data Exchange (ETDEWEB)

    Hori, K.; Iwama, A.; Fukuda, T.

    1985-12-01

    A simple method to evaluate the adhesive force between solid oxidizer and polymeric fuel-binder is presented. As an illustration, hydroxyl-terminated polybutadiene (HTPB) sticks including several different bonding agents are bonded on ammonium perchlorate (AP) single crystals, and stress-strain history unitl rupture occurs is obtained by applying uniaxial tensile stress perpendicularly to the adhesion surface. Further, whether each bonding agent reacts with AP or not was analysed with pursuing infrared absorption spectra. The hypothesis that the interfacial adhesive force arises from hydrogen bonding force is proposed.

  9. Analysis of perchlorate in foods and beverages by ion chromatography coupled with tandem mass spectrometry (IC-ESI-MS/MS)

    International Nuclear Information System (INIS)

    A new IC-ESI-MS/MS method, with simple sample preparation procedure, has been developed for quantification and confirmation of perchlorate (ClO4-) anions in water, fresh and canned food, wine and beer samples at low part-per-trillion (ng l-1) levels. To the best of our knowledge, this is the first time an analytical method is used for determination of perchlorate in wine and beer samples. The IC-ESI-MS/MS instrumentation consisted of an ICS-2500 ion chromatography (IC) system coupled to either an API 2000TM or an API 3200TM mass spectrometer. The IC-ESI-MS/MS system was optimized to monitor two pairs of precursor and fragment ion transitions, i.e., multiple reaction monitoring (MRM). All samples had oxygen-18 isotope labeled perchlorate internal standard (ISTD) added prior to extraction. Chlorine isotope ratio (35Cl/37Cl) was used as a confirmation tool. The transition of 35Cl16O4- (m/z 98.9) into 35Cl16O3- (m/z 82.9) was monitored for quantifying the main analyte; the transition of 37Cl16O4- (m/z 100.9) into 37Cl16O3- (m/z 84.9) was monitored for examining a proper isotopic abundance ratio of 35Cl/37Cl; and the transition of 35Cl18O4- (m/z 107.0) into 35Cl18O3- (m/z 89.0) was monitored for quantifying the internal standard. The minimum detection limit (MDL) for this method in de-ionized water is 5 ng l-1 (ppt) using the API 2000TM mass spectrometer and 0.5 ng l-1 using the API 3200TM mass spectrometer. Over 350 food and beverage samples were analyzed mostly in triplicate. Except for four, all samples were found to contain measurable amounts of perchlorate. The levels found ranged from 5 ng l-1 to 463.5 ± 6.36 μg kg-1 using MRM 98.9 → 82.9 and 100 μl injection

  10. cis-Aquabis(2,2′-bipyridine-κ2N,N′fluoridochromium(III bis(perchlorate dihydrate

    Directory of Open Access Journals (Sweden)

    Torben Birk

    2010-02-01

    Full Text Available The title mixed aqua–fluoride complex, [CrF(C10H8N22(H2O](ClO42·2H2O, has been synthesized by aquation of the corresponding difluoride complex using lanthanide(III ions as F− acceptors. The complex crystallizes with a CrIII ion at the center of a distorted octahedral coordination polyhedron with a cis arrangement of ligands. The crystal packing shows a hydrogen-bonding pattern involving water molecules, the coordinated F atom and the perchlorate anions

  11. Chromium solubility in anhydrous Phase B

    Science.gov (United States)

    Bindi, Luca; Sirotkina, Ekaterina A.; Bobrov, Andrey V.; Nestola, Fabrizio; Irifune, Tetsuo

    2016-02-01

    The crystal structure and chemical composition of a crystal of (Mg14- x Cr x )(Si5- x Cr x )O24 ( x ≈ 0.30) anhydrous Phase B (Anh-B) synthesized in the model system MgCr2O4-Mg2SiO4 at 12 GPa and 1600 °C have been investigated. The compound was found to be orthorhombic, space group Pmcb, with lattice parameters a = 5.900(1), b = 14.218(2), c = 10.029(2) Å, V = 841.3(2) Å3 and Z = 2. The structure was refined to R 1 = 0.065 using 1492 independent reflections. Chromium was found to substitute for both Mg at the M3 site (with a mean bond distance of 2.145 Å) and Si at the octahedral Si1 site (mean bond distance: 1.856 Å), according to the reaction Mg2+ + Si4+ = 2Cr3+. Such substitutions cause a reduction in the volume of the M3 site and an increase in the volume of the Si-dominant octahedron with respect to the values typically observed for pure Anh-B and Fe2+-bearing Anh-B. Taking into account that Cr3+ is not expected to be Jahn-Teller active, it appears that both the Cr3+-for-Mg and Cr3+-for-Si substitutions in the Anh-B structure decrease the distortion of the octahedra. Electron microprobe analysis gave the Mg13.66(8)Si4.70(6)Cr0.62(4)O24 stoichiometry for the studied phase. The successful synthesis of this phase provides new information for the possible mineral assemblages occurring in the Earth's deep upper mantle and shed new light on the so-called X discontinuity that has been observed at 275-345 km depth in several subcontinental and subduction zone environments.

  12. Scientific Opinion on chromium(III lactate tri-hydrate as a source of chromium added for nutritional purposes to foodstuff

    Directory of Open Access Journals (Sweden)

    EFSA Panel on Food Additives and Nutrient Sources added to Food (ANS

    2012-10-01

    Full Text Available

    The Panel on Food Additives and Nutrient Sources added to Food provides a scientific opinion on the safety and bioavailability of chromium(III lactate tri-hydrate as a source of chromium(III added for nutritional purposes to foodstuffs. The safety of chromium itself, in terms of the amounts that may be consumed, is outside the remit of this Panel. No new data have been provided as regards the safety and bioavailability of chromium from chromium(III lactate tri-hydrate. The Panel concurs with its earlier views stating that no evidence was provided supporting the bioavailability of chromium from chromium(III lactate tri-hydrate. Chromium(III lactate tri-hydrate is claimed to be freely soluble in water, however, chromium(III lactate tri-hydrate exists as a weak complex that may influence the bioavailability of chromium(III in the gastrointestinal tract. The Panel re-iterates that because of the complex chemistry of chromium(III lactate tri-hydrate in aqueous solutions and its limited solubility at pH >5, the bioavailability of chromium(III from chromium(III lactate tri-hydrate is low. Based on a conservative exposure estimate, the Panel calculated the combined intake of chromium(III from supplements and from foods fortified with chromium(III lactate tri-hydrate, for both adults and children, to be approximately 240 μg chromium(III/day, which is below the value of 250 µg/day established by the WHO for supplemental intake of chromium that should not be exceeded. The Panel noted that the use of chromium(III lactate tri-hydrate in the form of a premix with lactose, added to foods, would result in an exposure at the mean for adults of approximately 7-37 mg lactose/day (0.12-0.62 μg lactose/kg bw/day and to 36-192 μg lactate/day (0.60-3.20 μg/kg bw/day. Given that subjects with lactose maldigestion will tolerate up to 12 g of lactose with no or minor symptoms, these levels are not of safety concern.

  13. Biosorption of hexavalent chromium in a tannery industry wastewater using fungi species

    OpenAIRE

    Sivakumar, D.

    2016-01-01

    The isolated fungi species of different kinds from chromium contaminated soil sites located in Nagalkeni, Chennai were used for reducing chromium(VI) in a tannery industry wastewater of Nagalkeni, Chennai.  The experiments were conducted to know biosorption potential of isolated fungi species for removing chromium(VI) in a tannery industry wastewater against the different pH, fungi biomass and chromium(VI) concentration (dilution ratio).  The results of this study indicated that the order of ...

  14. Investigation of hexavalent chromium removal from Synthetic wastewater by using Peaganum

    OpenAIRE

    Ali Akbar Taghizadeh; Maryam khodadadi; Taher Shahriary; Hadighe Dorri; mahla zaferanieh; rasoul khosravi

    2012-01-01

    Background and Aim: Discharge of industrial wastewater containing hexavalent chromium into the environment can have harmful effects to the types of organisms. So, chromium should remove before discharging to the environment with an effective method. The purpose of this study of is hexavalent chromium removed with Peganum harmala granular seeds(PGS).   Materials and Methods: In this experimental study, The removal of hexavalent chromium with using PGS, with changes in time, pH, adsorbent dose,...

  15. Chromium Exposure and Hygienic Behaviors in Printing Workers in Southern Thailand

    OpenAIRE

    Somsiri Decharat

    2015-01-01

    Objectives. The main objective of this study was to assess the chromium exposure levels in printing workers. The study evaluated the airborne, serum, and urinary chromium levels and determines any correlation between level of chromium in specimen and airborne chromium levels. Material and Methods. A cross-sectional study was conducted with 75 exposed and 75 matched nonexposed subjects. Air breathing zone was measured by furnace atomic absorption spectrophotometer. Serum and urine samples were...

  16. Structure and morphology studies of chromium film at elevated temperature in hypersonic environment

    OpenAIRE

    Hegde, GM; Kulkarni, V; Nagaboopathy, M; Reddy, KPJ

    2012-01-01

    This paper presents the after shock heated structural and morphological studies of chromium film coated on hypersonic test model as a passive drag reduction element. The structural changes and the composition of phases of chromium due to shock heating (2850 K) are characterized using X-ray diffraction studies. Surface morphology changes of chromium coating have been studied using scanning electron microscopy (SEM) before and after shock heating. Significant amount of chromium ablation and sub...

  17. Cutaneous absorption of trivalent chromium: tissue levels and treatment by exchange transfusion

    OpenAIRE

    Kelly, W F; Ackrill, P; Day, J P; O'Hara, Maureen; Tye, C T; Burton, I.; Orton, C.; Harris, M.

    1982-01-01

    ABSTRACT A man was accidentally immersed in hot acidic trivalent chromium sulphate solution but none was swallowed. The clinical course was dominated by burns, intravascular haemolysis, and acute renal failure. Blood concentrations of chromium were measured during treatment and tissue concentrations were measured at death. Exchange transfusion reduced blood chromium concentrations by two-thirds. The total quantities of chromium absorbed and removed by various routes were calculated. In-vitro ...

  18. The risk to groundwater from wastewater irrigation using high chromium tannery effluent

    OpenAIRE

    Stuart, M E; Milne, C. J.

    2001-01-01

    Wastewater from Leon containing high concentrations of chromium from the tanning industry is used to irrigate agricultural land overlying an aquifer used for to supply potable water. Chromium from irrigation water is accumulating in agricultural soils, and in the lagoon and canal sediments, but groundwater appears to be unaffected and chromium concentrations remain low. A limited area of very high chromium concnetrations in groundwater was confirmed to be derived from a factory supplying the ...

  19. High-nitrogen-based pyrotechnics: longer- and brighter-burning, perchlorate-free, red-light illuminants for military and civilian applications.

    Science.gov (United States)

    Sabatini, Jesse J; Nagori, Amita V; Chen, Gary; Chu, Phillip; Damavarapu, Reddy; Klapötke, Thomas M

    2012-01-01

    The full-up prototype testing of perchlorate-free, hand-held, signal illuminants for the US Army's M126A1 red star parachute hand-held signal is described. Compared to the perchlorate-containing control, the disclosed illuminants yielded excellent stabilities toward various ignition stimuli while offering superior pyrotechnic performance. Militarily, the illuminants provided further evidence that development of smaller hand-held signal items in an environmentally conscious way is a realistic and obtainable goal. The results are also important from the perspective of civilian fireworks, as the development of brighter, longer-burning, and environmentally compatible red-light-emitting pyrotechnics is now possible. PMID:22161957

  20. A Hydrogen Ion-Selective Poly(Vinyl Chloride) Membrane Electrode Based on Calix[4]arene as a Perchlorate Ion-Selective Electrode

    OpenAIRE

    CANEL, Esin; ERDEN, Sevcan; ÖZEL, Ayça DEMİREL; MEMON, Sahahabuddin

    2008-01-01

    A hydrogen ion-selective electrode was prepared using 5,11,17,23-tetra-tert-butyl-25,26,27,28-tetracyanometoxy-calix[4]arene and the possibility of its use as a perchlorate ion-selective electrode was investigated using its characteristic of becoming perchlorate sensitive in acidic regions. The electrode of the optimum characteristic had a composition of 1% ionophore, 66% o-NPOE, and 33% PVC. This electrode exhibited a linear response over the range 1.0 \\times 10-1-1.0 \\times 10-5 M o...