WorldWideScience

Sample records for chlorates

  1. Characterization of the chlorate reductase from Pseudomonas chloritidismutans

    NARCIS (Netherlands)

    Wolterink, A.F.W.M.; Schiltz, E.; Hagedoorn, P.L.; Hagen, W.R.; Kengen, S.W.M.; Stams, A.J.M.

    2003-01-01

    A chlorate reductase has been purified from the chlorate-reducing strain Pseudomonas chloritidismutans. Comparison with the periplasmic (per)chlorate reductase of strain GR-1 showed that the cytoplasmic chlorate reductase of P. chloritidismutans reduced only chlorate and bromate. Differences were al

  2. Chlorate analyses in matrices of animal origin

    Science.gov (United States)

    Sodium chlorate is being developed as a potential food-safety tool for use in the livestock industry because of its effectiveness at decreasing concentrations of certain Gram-negative pathogens in gastrointestinal tracts of food animals. A number of studies with sodium chlorate in animals have demon...

  3. Reversed flow injection spectrophotometric determination of chlorate.

    Science.gov (United States)

    Chuesaard, Thanyarat; Wonganan, Tharinee; Wongchanapiboon, Teerapol; Liawruangrath, Saisunee

    2009-09-15

    An interfacing has been developed to connect a spectrophotometer with a personal computer and used as a readout system for development of a simple, rapid and sensitive reversed flow injection (rFI) procedure for chlorate determination. The method is based on the oxidation of indigo carmine by chlorate ions in an acidic solution (dil. HCl) leading to the decrease in absorbance at 610 nm. The decrease in absorbance is directly related to the chlorate concentration present in the sample solutions. Optimum conditions for chlorate were examined. A linear calibration graph over the range of 0.1-0.5 mg L(-1) chlorate was established with the regression equation of Y=104.5X+1.0, r(2)=0.9961 (n=6). The detection limit (3 sigma) of 0.03 mg L(-1), the limit of quantitation (10 sigma) of 0.10 mg L(-1) and the RSD of 3.2% for 0.3 mg L(-1) chlorate (n=11) together with a sample throughput of 92 h(-1) were obtained. The recovery of the added chlorate in spiked water samples was 98.5+/-3.1%. Major interferences for chlorate determination were found to be BrO(3)(-), ClO(2)(-), ClO(-) and IO(3)(-) which were overcome by using SO(3)(2-) (as Na(2)SO(3)) as masking agent. The method has been successfully applied for the determination of chlorate in spiked water samples with the minimum reagent consumption of 14.0 mL h(-1). Good agreement between the proposed rFIA and the reference methods was found verified by Student's t-test at 95% confidence level. PMID:19615529

  4. Current efficiency in the chlorate cell process

    Directory of Open Access Journals (Sweden)

    Spasojević Miroslav D.

    2014-01-01

    Full Text Available A mathematical model has been set up for current efficiency in a chlorate cell acting as an ideal electrochemical tubular reactor with a linear increase in hypochlorite concentration from the entrance to the exit. Good agreement was found between the results on current efficiency experimentally obtained under simulated industrial chlorate production conditions and the theoretical values provided by the mathematical model. [Projekat Ministarstva nauke Republike Srbije, br. 172057 i br. 172062

  5. Kinetics and disposition of orally dosed sodium chlorate in sheep

    Science.gov (United States)

    Experiments were conducted in sheep to determine excretory characteristics of sodium chlorate after a single oral dose. In Exp. 1 lambs (n = 16; age = 8.1 ± 1.7 d; BW = 8.2 ± 1.1 kg; mean ± SD) were dosed orally with 0, 30, 60, or 90 mg/kg BW of sodium chlorate. Twenty-four h after exposure chlorate...

  6. Pharmacokinetics of ruminally-dosed sodium chlorate in beef cattle

    Science.gov (United States)

    The recently recognized potential of sodium chlorate as a possible pre-harvest food safety tool in meat animals has spurred interest in the pharmacokinetics of intraruminally-dosed chlorate. Six Loala cattle were assigned (one heifer and one steer per treatment) to one of three intraruminal doses of...

  7. MECHANISM OF CHLORATE FORMATION IN CHLORINE DIOIXDE DELIGNIFICATION

    Institute of Scientific and Technical Information of China (English)

    Byung-Ho Yoon; Li-Jun Wang; Se-Jong Kim

    2004-01-01

    The effect of pH on chlorate formation during chlorine dioxide delignification of oxygen delignified kraft pulp was studied. Chlorate formation was found to increase slightly when pH was increased from 1.8 to 2.5, further increase of pH decreased chlorate formation.The above phenomenon is explained by the combination of two mechanisms, one by the reaction between hypochlorous acid and chlorite, another by the effect of chlorine on the regeneration of chlorine dioxide. The first mechanism suggests that chlorate formation is highly dependent on HCIO concentration which decreases with increasing pH and causes chlorate formation to behave in the same trend. The second mechanism suggests that chlorine favors the regeneration of chlorine dioxide while HCIO favors chlorate formation, thus lowering the pH from about 4 to the acidic end should decreases chlorate formation. The two opposite effects lead to the maximum formation of chlorate at around pH 2.5.

  8. MECHANISM OF CHLORATE FORMATION IN CHLORINE DIOIXDE DELIGNIFICATION

    Institute of Scientific and Technical Information of China (English)

    Byung-HoYoon; Li-JunWangI; Se-JongKim

    2004-01-01

    The effect of pH on chlorate formation duringchlorine dioxide delignification of oxygen delignifiedkraft pulp was studied. Chlorate formation was foundto increase slightly when pH was increased from 1.8to 2.5, further increase of pH decreased chlorateformation.The above phenomenon is explained by thecombination of two mechanisms, one by the reactionbetween hypochlorous acid and chlorite, another bythe effect of chlorine on the regeneration of chlorinedioxide. The first mechanism suggests that chlorateformation is highly dependent on HC10concentration which decreases with increasing pHand causes chlorate formation to behave in the sametrend. The second mechanism suggests that chlorinefavors the regeneration of chlorine dioxide whileHCIO favors chlorate formation, thus lowering thepH from about 4 to the acidic end should decreaseschlorate formation. Thethe maximum formation2.5.two opposite effects lead toof chlorate at around pH

  9. Manufacturing of soda chlorate by electrolysis of sodium chloride with graphite anodes; Fabrication du chlorate de soude par electrolyse du chlorure de sodium avec anodes en graphite

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1983-12-31

    Liquors containing soda chlorate and sodium chloride are injected into electrolyzers which transform chloride into chlorate with titanium anodes. The resulting liquors are then sent to a crystallizing pond where part of the chlorate is recovered. The remaining part is returned to the electrolyzers after addition of sodium chloride.

  10. Chlorate Concentration in the Jejunum and Cecum in Growing Pigs when Supplemented in Drinking Water

    Science.gov (United States)

    Prior research has demonstrated that oral administration of chlorate and nitrate results in reduced risk and / or concentration of Salmonella enterica fecal shedding of infected pigs, poultry and ruminants. The effect of chlorate is concentration dependent in vitro, but the concentrations of chlorat...

  11. Analytical Method for the Determination of Chlorate in Animal Matrices

    Science.gov (United States)

    Contamination of meat products with gram-negative enteric pathogens contribute to over 1.5 million food borne illnesses each year. Recent studies have demonstrated 2-3 log unit reductions in numbers of E. coli O157:H7 and(or) Salmonella in food animals dosed with an experimental chlorate-containing ...

  12. Total radioactive residues and residues of [36Cl]chlorate in market size broilers.

    Science.gov (United States)

    Smith, David J; Byrd, James A; Anderson, Robin C

    2007-07-11

    The oral administration of chlorate salts reduces the numbers of Gram-negative pathogens in gastrointestinal tracts of live food animals. Although the efficacy of chlorate salts has been demonstrated repeatedly, the technology cannot be introduced into commercial settings without first demonstrating that chlorate residues, and metabolites of chlorate remaining in edible tissues, represent a negligible risk to consumers. Typically, a first step in this risk assessment is to quantify the parent compound and to identify metabolites remaining in edible tissues of animals treated with the experimental compound. The objectives of this study were to determine the pathway(s) of chlorate metabolism in market broilers and to determine the magnitude of chlorate residues remaining in edible tissues. To this end, 12 broilers (6 weeks; 2.70+/-0.34 kg) were randomly assigned to three treatments of 7.4, 15.0, and 22.5 mM sodium [36Cl]chlorate dissolved in drinking water (n=4 broilers per treatment). Exposure to chlorate, dissolved in drinking water, occurred at 0 and 24 h (250 mL per exposure), feed was withdrawn at hour 38, water was removed at hour 48, and birds were slaughtered at hour 54 (16 h after feed removal and 8 h after water removal). The radioactivity was rapidly eliminated in excreta with 69-78% of the total administered radioactivity being excreted by slaughter. Total radioactive residues were proportional to dose in all edible tissues with chloride ion comprising greater than 98.5% of the radioactive residue for the tissue (9.4-97.8 ppm chlorate equivalents). Chlorate residues were typically greatest in the skin (0.33-0.82 ppm), gizzard (0.1-0.137 ppm), and dark muscle (0.05-0.14 ppm). Adipose, liver, and white muscle tissue contained chlorate concentrations from 0.03 to 0.13 ppm. In contrast, chlorate concentrations in excreta eliminated during the 6 h period prior to slaughter ranged from 53 to 71 ppm. Collectively, these data indicate that broilers rapidly

  13. EFFECT OF SODIUM [36CL]CHLORATE DOSE ON TOTAL RADIOACTIVE RESIDUES AND RESIDUES OF PARENT CHLORATE IN GROWING SWINE

    Science.gov (United States)

    An experimental chlorate-based product has shown to be efficacious in eliminating economically important, Gram-negative human pathogens in the gastrointestinal tracts of food animals. Prior to the commercial marketing of such a product, the magnitude and chemical nature of residues remaining in edib...

  14. Invited review: Efficacy, metabolism, and toxic responses to chlorate salts in food and laboratory animals.

    Science.gov (United States)

    Smith, D J; Oliver, C E; Taylor, J B; Anderson, R C

    2012-11-01

    For over 100 yr, scientists have explored uses of sodium chlorate in agricultural applications. Sodium chlorate is a strong oxidizer, and thus can be very hazardous when not handled accordingly. Nevertheless, late 19th century agriculturists and scientists attempted to exploit the chemical properties of sodium chlorate as an herbicide and food preservative. It is the herbicidal utility that led to subsequent use of sodium chlorate in the agricultural industry since then. However, in 2000, USDA-ARS scientists proposed a new and targeted use of sodium chlorate against enterobacteria in food animal production. Specifically, when orally dosed in to cattle (Bos taurus), swine (Sus scrofa), broilers (Gallus gallus), turkeys (Meleagris gallopavo), and sheep (Ovis aries), chlorate reduced the fecal shedding of common enteropathogens of the Enterobacteriaceae family. Subsequent to this discovery, the efficacy of chlorate salts has been demonstrated in numerous production classes within species. Doses of sodium chlorate as low as 30 mg/kg BW, but typically 50 to 150 mg/kg BW, have been used to demonstrate efficacy against pathogens. Single or short-duration (food animals. In all species studied to date, the major biotransformation product of chlorate is chloride ion; chlorite is not present in tissues or excreta of chlorate dosed animals. Chlorate is rapidly eliminated in ruminants and nonruminants, primarily in urine; likewise, residual chlorate in tissues depletes rapidly. Application of any new chemical entity to food animal production carries with it a responsibility to understand adverse reactions that intended and nonintended exposures may have in target and (or) nontarget animals and an understanding of the pathways of elimination that occur after exposure. Therefore, the purpose of this review is to summarize the published data regarding the efficacy, metabolism, and toxicology of chlorate salts in target (livestock) and nontarget species.

  15. 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

  16. Efficacy, metabolism, and toxic responses to chlorate salts in food and laboratory animals

    Science.gov (United States)

    For over 100 years, scientists have explored uses of sodium chlorate in agricultural applications. Sodium chlorate is a strong oxidizer, and thus can be very hazardous when not handled accordingly. Nevertheless, late 19th century agriculturists and scientists attempted to exploit the chemical proper...

  17. Chlorate reduction in the brine circuit of a chlor-alkali electrolysis. Chlorat-Reduktion im Solekreislauf einer Chlor-Alkali-Elektrolyse

    Energy Technology Data Exchange (ETDEWEB)

    Rodermund, R.

    1983-02-25

    The influence of reactant concentrations and temperature on the rate and selectivity of the chlorate/hydrochloric acid reaction was determined experimentally. A model equation system was derived on the basis of a reaction mechanism describing the reaction between chlorate and hydrochloric acid at high H/sup +/ and Cl/sup -/ concentrations in the temperature range between 40 and 90/sup 0/C. The reaction of chlorate and hydrochloric acid was found to be sufficient to maintain a low chlorate level in the brine circuit of a chlor-alkali electrolysis. ClO/sub 2/ formation is negligible if suitable reaction conditions are chosen. Further, a model equation based on Henry's law was established for the solubility of ClO/sub 2/ in mixed solutions of HCl and NaCl in the temperature range of 40 to 90/sup 0/C.

  18. Minimising chlorate in the electrolytic disinfection of irrigation water

    Directory of Open Access Journals (Sweden)

    Ingo Schuch

    2016-03-01

    Full Text Available Die Minimierung von Chlorat bei der elektrolytischen Gießwasserdesinfektion ist aufgrund problematischer Chloratrückstände in pflanzlichen Lebensmitteln von Bedeutung. Im Hinblick auf verfahrenstechnische Optimierungsvorschläge wurde daher am Beispiel einer Salzelektrolyseanlage (Einkammersystem geprüft, wie viel Chlorat beim Herstellungsprozess des Desinfektionsmittels entsteht und wie sich dessen Anteil bei einer Lagerung unter warmen Temperaturbedingungen im Gewächshaus verändert. Zudem wurde untersucht, wie sich der Pflanzendünger Ammonium auf das Desinfektionsmittel auswirkt. Dabei ergab sich, dass die Chloratbildung durch eine Kühlung des Elektrolysereaktors sowie des Desinfektionsmitteltanks und durch ein zur Kurzzeitlagerung ausgelegtes Bevorratungssystem von Desinfektionsmittel minimiert werden könnte. Ferner wurde bestätigt, dass Ammonium den Desinfektionsmittelverbrauch bzw. Chlorateintrag deutlich erhöht. Daher empfiehlt sich eine sensorbasierte Dosierung, um sich ändernde chemische Vorgänge im Gießwasser (Chlorzehrung zu berücksichtigen.

  19. Why chlorate occurs in potable water and processed foods: a critical assessment and challenges faced by the food industry.

    Science.gov (United States)

    Kettlitz, Beate; Kemendi, Gabriella; Thorgrimsson, Nigel; Cattoor, Nele; Verzegnassi, Ludovica; Le Bail-Collet, Yves; Maphosa, Farai; Perrichet, Aurélie; Christall, Birgit; Stadler, Richard H

    2016-06-01

    Recently, reports have been published on the occurrence of chlorate mainly in fruits and vegetables. Chlorate is a by-product of chlorinating agents used to disinfect water, and can be expected to be found in varying concentrations in drinking water. Data on potable water taken at 39 sampling points across Europe showed chlorate to range from foods of 0.01 mg kg(-1). This default MRL has now led to significant problems in the EU, where routinely disinfected water, used in the preparation of food products such as vegetables or fruits, leaves chlorate residues in excess of the default MRL, and in strict legal terms renders the food unmarketable. Due to the paucity of data on the chlorate content of prepared foods in general, we collated chlorate data on more than 3400 samples of mainly prepared foods, including dairy products, meats, fruits, vegetables and different food ingredients/additives. In total, 50.5% of the food samples contained chlorate above 0.01 mg kg(-1), albeit not due to the use of chlorate as a pesticide but mainly due to the occurrence of chlorate as an unavoidable disinfectant by-product. A further entry point of chlorate into foods may be via additives/ingredients that may contain chlorate as a by-product of the manufacturing process (e.g. electrolysis). Of the positive samples in this study, 22.4% revealed chlorate above 0.1 mg kg(-1). In the absence of EU levels for chlorate in water, any future EU regulations must consider the already available WHO guideline value of 0.7 mg l(-1) in potable water, and the continued importance of the usage of oxyhalides for disinfection purposes.

  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. Fe-Mo alloy coatings as cathodes in chlorate production process

    Directory of Open Access Journals (Sweden)

    Gajić-Krstajić Ljiljana M.

    2016-01-01

    Full Text Available The aim of this study was to gain a better understanding of the feasibility of partial replacement of dichromate, Cr(VI, with phosphate buffer, focusing on the cathode reaction selectivity for hydrogen evolution on mild steel and Fe-Mo cathodes in undivided cell for chlorate production. To evaluate the ability of phosphate and Cr(VI additions to hinder hypochlorite and chlorate reduction, overall current efficiency (CE measurements in laboratory cell for chlorate production on stationary electrodes were performed. The concentration of hypochlorite was determined by a conventional potentiometric titration method using 0.01 mol dm-3 As2O3 solution as a titrant. The chlorate concentration was determined by excess of 1.0 mol dm-3 As2O3 solution and excess of arsenic oxide was titrated with 0.1 mol dm-3 KBrO3 solution in a strong acidic solution. Cathodic hypochlorite and chlorate reduction were suppressed efficiently by addition of 3 g dm-3 dichromate at both cathodes, except that Fe-Mo cathode exhibited higher catalytic activity for hydrogen evolution reaction (HER. The overvoltage for the HER was around 0.17 V lower on Fe-Mo cathode than on mild steel at the current density of 3 kA m-2. It was found that a dichromate content as low as 0.1 g dm-3 is sufficient for complete suppression of cathodic hypochlorite and chlorate reduction onto Fe-Mo catalyst in phosphate buffering system (3 g dm-3 Na2HPO4 + NaH2PO4. The overall current efficiency was practically the same as in the case of the presence of 3 g dm-3 dichromate buffer (98 %. However, for the mild steel cathode, the overall current efficiency for the chlorate production was somewhat lower in the above mentioned mixed phosphate + dichromate buffering system (95% than in the pure dichromate buffering solution (97.5%.

  2. Continuous, low-dose oral exposure to sodium chlorate reduces fecal Enterobacteriaceae coliforms in sheep feces without inducing subclinical chlorate toxicosis

    Science.gov (United States)

    Our objectives were to determine a minimal daily dose of sodium chlorate, to be included in the drinking water for 5 days, that is safe yet maintains efficacy in reducing fecal shedding of Escherichia coli in mature ewes. In a complete randomized experimental design, 25 Targhee ewes (age = 18- to 20...

  3. Clorate Metabolism in Pure Cultures of E.Coli 0157:H7 Pretreated with Either Nitrate or Chlorate

    Science.gov (United States)

    Experiments were conducted to determine the effects of 5, 7.5, and 10 mM nitrate, and 5, 10, or 20 mM chlorate on total E. coli counts, chlorate metabolism, and volatile fatty acid (VFA) concentrations in anaerobic ruminal fluid cultures. Nitrate did not affect total E. coli counts (P = 0.05), chlor...

  4. Evaluation of an experimental sodium chlorate product, with and without nitroethane, on Salmonella in cull dairy cattle

    Science.gov (United States)

    Ruminant animals are natural reservoirs for Salmonella. These bacteria can reduce nitrate to nitrite through the membrane bound enzyme nitrate reductase which also has the ability to reduce chlorate to the cytotoxic end-product chlorite. An experimental product containing sodium chlorate (ECP) has...

  5. Foliar fertilization as an alternative to hand thinning fruit in chlorate treated Dimocarpus longan Lour. trees in Hawaii.

    Science.gov (United States)

    Longan, Dimocarpus longan Lour, is a member of the Sapindaceae, a family that also includes lychee, and rambutan. The discovery of potassium chlorate (KClO3) induced flowering solved the problem of alternate bearing and enabled the grower to produce off-season longan. Chlorate treatments commonly i...

  6. 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

  7. Physiological and phylogenetic characterization of a stable chlorate-reducing benzene-degrading microbial community

    NARCIS (Netherlands)

    Weelink, S.A.B.; Tan, N.C.G.; Broeke, ten H.; Doesburg, van W.C.J.; Langenhoff, A.A.M.; Gerritse, J.; Stams, A.J.M.

    2007-01-01

    stable anoxic enrichment culture was obtained that degraded benzene with chlorate as an electron acceptor. The benzene degradation rate was 1.65 mM benzene per day, which is similar to reported aerobic benzene degradation rates but 20¿1650 times higher than reported for anaerobic benzene degradation

  8. Influence of drinking water treatments on chlorine dioxide consumption and chlorite/chlorate formation.

    Science.gov (United States)

    Sorlini, Sabrina; Gialdini, Francesca; Biasibetti, Michela; Collivignarelli, Carlo

    2014-05-01

    Disinfection is the last treatment stage of a Drinking Water Treatment Plant (DWTP) and is carried out to maintain a residual concentration of disinfectant in the water distribution system. Chlorine dioxide (ClO2) is a widely used chemical employed for this purpose. The aim of this work was to evaluate the influence of several treatments on chlorine dioxide consumption and on chlorite and chlorate formation in the final oxidation/disinfection stage. A number of tests was performed at laboratory scale employing water samples collected from the DWTP of Cremona (Italy). The following processes were studied: oxidation with potassium permanganate, chlorine dioxide and sodium hypochlorite, coagulation/flocculation with ferric chloride and aluminum sulfate, filtration and adsorption onto activated carbon. The results showed that the chlorine dioxide demand is high if sodium hypochlorite or potassium permanganate are employed in pre-oxidation. On the other hand, chlorine dioxide leads to the highest production of chlorite and chlorate. The coagulation/flocculation process after pre-oxidation shows that chlorine dioxide demand decreases if potassium permanganate is employed as an oxidant, both with ferric chloride and aluminum sulfate. Therefore, the combination of these processes leads to a lower production of chlorite and chlorate. Aluminum sulfate is preferable in terms of the chlorine dioxide demand reduction and minimization of the chlorite and chlorate formation. Activated carbon is the most effective solution as it reduced the chlorine dioxide consumption by about 50% and the DBP formation by about 20-40%.

  9. Physiological and phylogenetic characterization of a stable benzene-degrading, chlorate-reducing microbial community

    NARCIS (Netherlands)

    Weelink, S.A.B.; Tan, N.C.G.; Broeke, H. ten; Doesburg, W. van; Langenhoff, A.A.M.; Gerritse, J.; Stams, A.J.M.

    2007-01-01

    A stable anoxic enrichment culture was obtained that degraded benzene with chlorate as an electron acceptor. The benzene degradation rate was 1.65 mM benzene per day, which is similar to reported aerobic benzene degradation rates but 20-1650 times higher than reported for anaerobic benzene degradati

  10. Control of sodium chlorate content in brine%盐水中氯酸钠含量的控银

    Institute of Scientific and Technical Information of China (English)

    韩飞; 张晓龙

    2011-01-01

    The source, hazards and control of sodium chlorate concentration in brine system were introduced. In order to ensure the decomposition efficiency of sodium chlorate and security of operation, the operation of chlorate decomposition and some notes were put%介绍了氯碱生产中盐水系统中氯酸钠的来源、危害及浓度的控制方法。为了保证氯酸钠的分解效率和操作安全性,对氯酸盐分解单元的操作及注意事项提出了建议。

  11. Contribution of tap water to chlorate and perchlorate intake: a market basket study.

    Science.gov (United States)

    Asami, Mari; Yoshida, Nobue; Kosaka, Koji; Ohno, Koichi; Matsui, Yoshihiko

    2013-10-01

    The contributions of water to total levels of chlorate and perchlorate intake were determined using food and water samples from a market basket study from 10 locations in Japan between 2008 and 2009. Foods were categorized into 13 groups and analyzed along with tap water. The average total chlorate intake was 333 (min. 193-max. 486) μg/day for samples cooked with tap water. The contribution of tap water to total chlorate intake was as high as 47%-58%, although total chlorate intake was less than 32% of the tolerable daily intake, 1500 μg/day for body weight of 50 kg. For perchlorate, daily intake from water was 0.7 (0.1-4.4) μg/day, which is not high compared to the average total intake of 14 (2.5-84) μg/day, while the reference dose (RfD) is 35 μg/day and the provisional maximum tolerable daily intake (PMTDI) is 500 μg/day for body weight of 50 kg. The highest intake of perchlorate was 84 μg/day, where concentrations in foods were high, but not in water. The contribution of water to total perchlorate intake ranged from 0.5% to 22%, while the ratio of highest daily intake to RfD was 240% and that to PMTDI was 17%. Eight baby formulas were also tested--total chlorate and perchlorate intakes were 147 (42-332) μg/day and 1.11 (0.05-4.5) μg/day, respectively, for an ingestion volume of 1 L/day if prepared with tap water.

  12. Technological transformation of chlorate decomposing tank%氯酸盐分解槽的工艺改造

    Institute of Scientific and Technical Information of China (English)

    封小洪; 蒲云彬

    2015-01-01

    介绍氯酸盐产生的原因及危害,分析分解槽分解效率不高的原因,给出工艺改进方案和采取的改造措施.%The formation causes and harm of chlorate were introduced. The causes of low decomposition rate of chlorate in decomposer were analyzed. Process improvement plans and reform measures taken were provided.

  13. Basal levels of pesticide organ chlorates in the plasma of dogs of Zaragoza, Spain

    International Nuclear Information System (INIS)

    During the month of January of 1992 they took samples of plasma in 83 dogs of the Center of Animal Protection of Zaragoza, Spain, specify their concentrations of pesticides organ chlorates. The biggest levels means were reached by the Endosulfan Sulfate and the Lindano, being also detected beta residuals and alpha - HCL, Endosulfan I and II, Dieldr and p,p - DDE. They have not been significant differences in the pesticides levels according to the sex, age or weight of it lauds animals

  14. 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

  15. EFSA CONTAM Panel (EFSA Panel on Contaminants in the Food Chain), 2015. Scientific Opinion on risks for public health related to the presence of chlorate in food

    DEFF Research Database (Denmark)

    Petersen, Annette

    Following a request from the European Commission, the risks to human health related to the presence of chlorate in food were assessed by the EFSA Panel on Contaminants in the Food Chain (CONTAM Panel). The presence of chlorate in food can arise from the use of chlorinated water for food processing...... and the disinfection of food-processing equipment. Inhibition of iodine uptake in humans was identified as the critical effect for chronic exposure to chlorate. A tolerable daily intake (TDI) of 3 µg chlorate/kg body weight (b.w.) was set by read-across from a TDI of 0.3 µg/kg b.w. derived for this effect...... for perchlorate, multiplied by a factor of 10 to account for the lower potency of chlorate. Formation of methaemoglobin was identified as the critical acute effect of chlorate. An acute reference dose (ARfD) of 36 µg chlorate/kg b.w. was derived from a no-observed-effect-level for chlorate in a controlled...

  16. OPTICAL DIAGNOSTIC AND MODELING SOLUTION GROWTH PROCESS OF SODIUM CHLORATE CRYSTALS

    Institute of Scientific and Technical Information of China (English)

    WANG Tao; DUAN Li

    2006-01-01

    Both a real time optical interferometric experiment and a numerical simulation of two-dimension non-steady state model were employed to study the growth process of aqueous sodium chlorate crystals. The parameters such as solution concentration distribution, crystal dimensions, growth rate and velocity field were obtained by both experiment and numerical simulation. The influence of earth gravity during crystal growth process was analyzed. A reasonable theory model corresponding to the present experiment is advanced. The thickness of concentration boundary layer was investigated especially. The results from the experiment and numerical simulation match well.

  17. (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.

  18. Evaluation of sodium chlorate as a pre-harvest intervention for controlling Salmonella in the peripheral lymph nodes of cattle

    Science.gov (United States)

    The objective of the current study was to evaluate sodium chlorate as a potential pre-harvest intervention for reducing or eliminating Salmonella from the peripheral lymph nodes of experimentally-infected cattle. The peripheral lymph nodes of Holstein steers (approx. BW = 160 kg; 4 and 6 head in co...

  19. Effect of intravenous or oral sodium chlorate administration on the fecal shedding of Escherichia coli in sheep

    Science.gov (United States)

    The effect of gavage or intravenous (i.v.) administration of sodium chlorate salts on the fecal shedding of generic Escherichia coli in wether lambs was studied. To this end, 9 lambs (27 +/- 2.5 kg) were administered 150 mg NaClO3 per kg BW by gavage or i.v. infusion in a cross-over design with sal...

  20. Ordinary Toxicity of Chlorine Dioxide and By-products Chlorite and Chlorate in Water

    Institute of Scientific and Technical Information of China (English)

    王丽; 常爱敏; 黄君礼

    2003-01-01

    Acute toxicity and accumulated toxicity of chlorine dioxide (C1O2) and by-products chlorite ( C1O-2 ) and chlorate (C1O-3) in water acted on mice are studied by the method of Horn and accumulation coefficient.Subchronic toxicity of the mixture of C1O2 and C1O-2 and ClO-3 in water acted on rat is studied though feeding test for 90 days, including statistical analysis of variance on weight gaining, food utilization efficiency, index of blood and serum, liver (or kidney)to body weight ratio, and histopathological examination on liver and kidney. The results show that aqueous solution of C1O2, NaC1O2 and NaC1O3 (with the concentration of 276. 5 mg/L, 200 mg/L and 200 mg/L respectively) and the mixed aqueous solution of C1O2 with the concentration of 553 mg/L are actually non poisonous, and non-cumulative aqueous solution as well.

  1. Zoonotic bacterial populations, gut fermentation characteristics and methane production in feedlot steers during oral nitroethane treatment and after the feeding of an experimental chlorate product

    Science.gov (United States)

    Nitroethane inhibits the growth of certain zoonotic pathogens such as Campylobacter and Salmonella spp., foodborne pathogens estimated to cause millions of human infections each year, and enhances the Salmonella- and E. coli-killing effect of an experimental chlorate product being developed as a fee...

  2. 氯酸盐电解槽废气的处理%Waste gas treatment of chlorate electrolyzers

    Institute of Scientific and Technical Information of China (English)

    许瑞光

    2011-01-01

    Based on the analysis about the waste gas produced from chlorate electrolyzers, waste gas treatment technology of chlorate electrolyzers was introduced as follows;firstly,content of chlorine in waste gas is reduced by 50% after pre-treatment;then,volume fraction of chlorine is below 2 × 10-5 through the absorption columns in series, whose absorber is NaOH solution;finally,by the deoxygenization column with palladium as catalyst and Al2O3 as carrier,the gas is transported to the next procedure through water-ring vacuum pump and compressor. Some attentive problems and appropriate measures in the process of waste gas treatment were put forward.%对氯酸盐电解槽废气的产生进行分析.介绍了电解槽废气处理的工艺:经过预处理,使气体中氯气含量降低50%,再经过以氢氧化钠溶液为氯气吸收剂的串联吸收塔,可使氯气体积分数达2×10-5以下;将该气体通过以钯为催化剂、三氧化二铝为载体的除氧塔进行处理,经水环式真空泵及压缩机输送至下一工序予以利用.提出了废气处理过程中应注意的问题以及应采取的措施.

  3. 氯酸钾制备膨胀石墨的研究%Preparation of Expanded Graphite by Potassium Chlorate

    Institute of Scientific and Technical Information of China (English)

    彭颖昊; 蒋述兴

    2012-01-01

    Low-temperature expandable graphite with high initial expansion temperature was prepared using the potassium chlorate as the solid oxidant. Reaction conditions was researched on the low-temperature expandable graphite swelling volume, the results showed that the initial expansion temperature was 260℃, and the expansion was up to 300 mL/g at 400℃ while taking 5 g of graphite, 0.6 g of potassium chlorate, 13.5 ml of concentrated sulfuric and 4.5 mL of concentrated nitricacid reacting 60 min at 20 ℃. The X-ray diffraction confirmed the formation of graphite intercalation compounds, and the SEM showed the microstructure of expanded graphite.%以氯酸钾为固体氧化剂,制备了高起始膨胀温度的低温可膨胀石墨.考察了反应条件对可膨胀石墨低温膨胀体积的影响,确定了最佳工艺条件:5g石墨配以0.6g氯酸钾、13.5 mL浓硫酸、4.5 mL浓硝酸、在20℃时反应60min.此条件下得到的可膨胀石墨起始膨张温度为260℃,在400℃时膨胀体积为300 mL/g.X射线衍射证实了石墨层间化合物的生成,并利用SEM扫描电镜分析了膨胀石墨的微观结构.

  4. 氯酸盐电解槽爆炸原因分析%Analysis of the reason of chlorate electrolyzer explosion

    Institute of Scientific and Technical Information of China (English)

    孙永泰

    2015-01-01

    The phenomenon and the reason of chlorate electrolyzer explosion in operation was analyzed. At the same time, the corresponding measures were put forward.%详细分析了氯酸盐电解槽在操作时发生爆炸的现象和原因,同时,也提出了应采取的相应措施。

  5. The Investigation of Chlorate and Perchlorate/Saponite Mixtures as a Possible Source of Oxygen and Chlorine Detected by the Sample Analysis at Mars (SAM) Instrument in Gale Crater

    Science.gov (United States)

    Clark, J.; Sutter, B.; Min, D. W.; Mahaffy, P.

    2016-01-01

    The Sample Analysis at Mars (SAM) instrument on board the Curiosity Rover has detected O2 and HCl gas releases from all analyzed Gale Crater sediments, which are attributed to the presence of perchlorates and/or chlorates in martian sediment. Previous SAM analog laboratory analyses found that most pure perchlorates and chlorates release O2 and HCl at different temperatures than those observed in the SAM data. Subsequent studies examined the effects of perchlorate and chlorate mixtures with Gale Crater analog iron phases, which are known to catalyze oxychlorine decomposition. Several mixtures produced O2 releases at similar temperatures as Gale Crater materials, but most of these mixtures did not produce significant HCl releases comparable to those detected by the SAM instrument. In order to better explain the Gale Crater HCl releases, perchlorates and chlorates were mixed with Gale Crater analog saponite, which is found at abundances from 8 to 20 wt % in the John Klein and Cumberland drill samples. Mixtures of chlorates or perchlorates with calcium-saponite or ferrian-saponite were heated to 1000 deg C in a Labsys EVO differential scanning calorimeter/mass spectrometer configured to operate similarly to the SAM oven/quadrupole mass spectrometer system. Our results demonstrate that all chlorate and perchlorate mixtures produce significant HCl releases below 1000 deg C as well as depressed oxygen peak release temperatures when mixed with saponite. The type of saponite (calcium or ferrian saponite) did not affect the evolved gas results significantly. Saponite/Mg-perchlorate mixtures produced two HCl releases similar to the Cumberland drilled sample. Mg-chlorate mixed with saponite produced HCl releases similar to the Big Sky drilled sample in an eolian sandstone. A mixture of Ca-perchlorate and saponite produced HCl and oxygen releases similar to the Buckskin mudstone drilled sample and the Gobabeb 2 eolian dune material. Ca-chlorate mixed with saponite produced both

  6. Enantioselective Crystallization of Sodium Chlorate in the Presence of Racemic Hydrophobic Amino Acids and Static Magnetic Fields

    Directory of Open Access Journals (Sweden)

    María-Paz Zorzano

    2014-06-01

    Full Text Available We study the bias induced by a weak (200 mT external magnetic field on the preferred handedness of sodium chlorate crystals obtained by slow evaporation at ambient conditions of its saturated saline solution with 20 ppm of added racemic (dl hydrophobic amino acids. By applying the Fisher test to pairs of experiments with opposing magnetic field orientation we conclude, with a confidence level of 99.7%, that at the water-air interface of this saline solution there is an enantioselective magnetic interaction that acts upon racemic mixtures of hydrophobic chiral amino acids. This interaction has been observed with the three tested racemic hydrophobic amino acids: dl-Phe, dl-Try and dl-Trp, at ambient conditions and in spite of the ubiquitous chiral organic contamination. This enantioselective magnetic dependence is not observed when there is only one handedness of added chiral amino-acid, if the added amino acid is not chiral or if there is no additive. This effect has been confirmed with a double blind test. This novel experimental observation may have implications for our view of plausible initial prebiotic scenarios and of the roles of the geomagnetic field in homochirality in the biosphere.

  7. The Investigation of Chlorates as a Possible Source of Oxygen and Chlorine Detected by the Sample Analysis at Mars (SAM) Instrument in Gale Crater, Mars

    Science.gov (United States)

    Sutter, B.; Archer, D. P.; Ming, D. W.; Niles, P. B.; Eigenbrode, J. L.; Franz, H.; Glavin, D. P.; McAdam, A. C.; Mahaffy, P; Stern, J. C.; Navarro-Gonzalez, R.; McKay, C. .P.

    2014-01-01

    The Sample Analysis at Mars (SAM) instrument onboard the Curiosity rover detect-ed 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 perchlorates has yet to provide an unequivocal temperature match to the SAM O2 and HCl release data. Iron mineralogy found in the Rocknest materials when mixed with Ca-perchlorate does cause O2 release temperatures to be closer match to the SAM O2 release data but more work is required in evaluating the catalytic effects of Fe mineralogy on perchlorate decomposition. Chlorates (ClO3-) are relevant Mars materials and potential O2 and Cl sources. The objective of this work is to evaluate the thermal decomposition of select chlorate (ClO3-) salts as possible sources of the O2 and HCl releases in the Gale Crater materials.

  8. 氯酸钠生产中母液处理工艺研究%Study on treatment process of mother liquor in sodium chlorate industry

    Institute of Scientific and Technical Information of China (English)

    郭淑芬; 周俊波; 潘胜

    2012-01-01

    Recently .chemical precipitation is used for treating sulfate radicals in the sodium chlorate production, but produces a considerable amount of sludge containing Cr,causing pollution to the environment.The use of ion exchange resin and nanofiltration membrane device integrated treatment of sodium chlorate industry crystallization mother liquor was presented.This method not only could recover sodium dichromate but also could remove sulfate radicals.Results showed that the recovery rate of sodium dichromate could reach 98%, and the content of sodium sulfate in the crystallization mother liquor was less than 3 g/L after treatment, reaching the recycling requirements.%目前,在氯酸钠生产中常用化学沉淀法处理硫酸根,但是会产生大量含铬污泥,污染环境.提出利用离子交换树脂和纳滤膜装置综合处理结晶母液的方法,既能回收重铬酸钠又能脱除硫酸根.实验结果表明,重铬酸钠的回收率可达98%,结晶母液处理后硫酸钠质量浓度低于3 g/L,达到母液循环利用的要求.

  9. The Investigation of Chlorate/Iron-Phase Mixtures as a Possible Source of Oxygen and Chlorine Detected by the Sample Analysis at Mars (SAM) Instrument in Gale Crater, Mars

    Science.gov (United States)

    Clark, J.; Sutter, B.; Morris, R. V.; Archer, P. D.; Ming, D. W.; Niles, P.; Mahaffy, P.; Navarro-Gonzalez, R.

    2016-01-01

    The Sample Analysis at Mars (SAM) instrument on board the Curiosity Rover has detected oxygen and HCl gas releases from all analyzed Gale Crater sediments. The presence of perchlorate ClO4(sup-) and/or chlorates ClO3(sup-) are potential sources of the aforementioned O2 releases. The detections of O2 and HCl gas releases and chlorinated hydrocarbons by SAM coupled with the detection of perchlorates by Phoenix Lander's 2008 Wet Chemistry Laboratory all suggest that perchlorates, and possibly chorates, may be present in the Gale Crater sediments. Previous laboratory studies have attempted to replicate these O2 releases by heating perchlorates and chlorates in instruments operated similarly to those in the SAM instrument. Early studies found that pure perchlorates release O2 at temperatures higher than those observed in SAM data. Subsequently, studies were done to test the effects of mixing iron-phase minerals, analogous to those detected on Mars by ChemMin, with perchlorates. The iron in these minerals acts as a catalyst and causes O2 to be released from the perchlorate at a lower temperature. These studies found that perchlorate solutions mixed with either Hawaii palagonite or ferrihydrite produce O2 releases at temperatures similar to the Rocknest (RN) windblown deposit and the John Klein (JK) drill sample from the Sheepbed mudstone. The study also determined that perchlorate mixtures with magnetite, hematite, fayalite-magnetite, ilmentite, and pyrrhotite produce O2 releases at temperatures similar to the Confidence Hills (CH) drill sample from the Murray mudstone. Oxygen re-leases from pure chlorates were recently compared with the SAM data. Laboratory analyses determined that Ca-chlorate produces O2 and HCl peaks that are similar to those detected in RN and JK materials. Currently, no perchlorate/chlorate mixture with iron-phase minerals can explain the O2 releases from either the Cumberland (CB) drill sample from the Sheepbed mudstone or Windjana (WJ) drill

  10. The influence of 2,3-dihydroxybenzaldehyde thiosemicarbazone on catalytic currents in the system molybdenum(VI) - potassium chlorate in acid sulfate solutions

    International Nuclear Information System (INIS)

    The polarographic catalytic current in acid solutions of Mo(VI), 2,3-dihydroxybenzaldehyde thiosemicarbazone (TSC 2,3-DHBA) and chlorate ions has been investigated. The scheme of reactions, taking place in the solutions and on the electrode, has been proposed. The increase of the catalytic current is explained by the formation of an active intermediate complex [Mo(V) TSC 2,3-DHBA (ClO-3)]. The rate constant of this complex formation K = 2.56x106 mol-1 dm3 s-1, the activation energy Ea = 15.9 kcal x mol-1 and the reaction activation entropy ΔSa≠ = -23.5 e.u. have been calculated. (authors)

  11. THE INFLUENCE OF THIOSEMICARBAZONE 2,3-DIHYDROXYBENZALDEHYDE ON CATALYTIC CURRENTS IN THE SYSTEM MOLYBDENUM (VI – POTASSIUM CHLORATE IN ACID SULFATE SOLUTIONS

    Directory of Open Access Journals (Sweden)

    Ludmila Chiriac

    2011-06-01

    Full Text Available The polarographic catalytic current in acid solutions of Mo(VI, thiosemicarbazone 2,3-dihydroxybenzaldehyde (TSC 2,3-DHBA and chlorate ions has been investigated. The scheme of reactions, taking place in the solutions and on the electrode, has been proposed. The increase of the catalytic current is explained by the formation of an active intermediate complex [Mo(V×TSC 2,3-DHBA (ClO-3]. The rate constant of this complex formation K = 2.56 × 106 mol-1×dm3×s-1, the activation energy Ea = 15.9 kcal×mol-1 and the reaction activation entropy ∆Sa¹ = -23.5 e.u. have been calculated.

  12. THREE WASTES TREATMENT IN THE PRODUCTION OF SODIUM CHLORATE.%氯酸钠生产中的三废处理

    Institute of Scientific and Technical Information of China (English)

    张广惠; 张玉生

    2001-01-01

    The treatment technology for the three wastes( water, gas and sludge)in the production of sodium chlorate is introduced. By practice, it proves that this technology is reasonable, the utilization ratio of resources is high and the pollution is decreased.%介绍万吨工业氯酸钠生产中废水、废气、废渣的处理技术,实践证明,三废治理的工艺是合理的,原料有效成分利用率高,节约了资源,减少了二次污染,各项指标均达到排放标准。

  13. Control of Sulfidogenesis Through Bio-oxidation of H2S Coupled to (per)chlorate Reduction

    Energy Technology Data Exchange (ETDEWEB)

    Gregoire, Patrick [Univ. of California, Berkeley, CA (United States); Engelbrektson, Anna [Univ. of California, Berkeley, CA (United States); Hubbard, Christopher G. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Metlagel, Zoltan [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Csencsits, Roseann [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Auer, Manfred [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Conrad, Mark E. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Thieme, Jurgen [Brookhaven National Lab. (BNL), Upton, NY (United States); Northrup, Paul [Brookhaven National Lab. (BNL), Upton, NY (United States); Coates, John D. [Univ. of California, Berkeley, CA (United States)

    2014-04-04

    Here, we investigate H2S attenuation by dissimilatory perchlorate-reducing bacteria (DPRB). All DPRB tested oxidized H2S coupled to (per)chlorate reduction without sustaining growth. H2S was preferentially utilized over organic electron donors resulting in an enriched (34S)-elemental sulfur product. Electron microscopy revealed elemental sulfur production in the cytoplasm and on the cell surface of the DPRB Azospira suillum. We also propose a novel hybrid enzymatic-abiotic mechanism for H2S oxidation similar to that recently proposed for nitrate-dependent Fe(II) oxidation. The results of this study have implications for the control of biosouring and biocorrosion in a range of industrial environments.

  14. Natural chlorate in the environment: Application of a new IC-ESI/MS/MS method with a Cl18O3- internal standard

    Science.gov (United States)

    Rao, Balaji; Hatzinger, Paul B.; Böhlke, John Karl; Sturchio, Neil C.; Andraski, Brian J.; Eckardt, Frank D.; Jackson, W. Andrew

    2010-01-01

    A new ion chromatography electrospray tandem mass spectrometry (IC-ESI/MS/MS) method has been developed for quantification and confirmation of chlorate (ClO3-) in environmental samples. The method involves the electro-chemical generation of isotopically labeled chlorate internal standard (Cl18O3-) using 18O water (H218O). The standard was added to all samples prior to analysis thereby minimizing the matrix effects that are associated with common ions without the need for expensive sample pretreatments. The method detection limit (MDL) for ClO3- was 2 ng L-1 for a 1 mL volume sample injection. The proposed method was successfully applied to analyze ClO3- in difficult environmental samples including soil and plant leachates. The IC-ESI/MS/MS method described here was also compared to established EPA method 317.0 for ClO3- analysis. Samples collected from a variety of environments previously shown to contain natural perchlorate (ClO 4-) occurrence were analyzed using the proposed method and ClO3- was found to co-occur with ClO4- at concentrations ranging from 500 mg kg-1 in caliche salt deposits from the Atacama Desert in Chile. Relatively low concentrations of ClO3- in some natural groundwater samples (-1) analyzed in this work may indicate lower stability when compared to ClO4- in the subsurface. The high concentrations of ClO3- in caliches and soils (3-6 orders of magnitude greater) as compared to precipitation samples indicate that ClO3-, like ClO4-, may be atmospherically produced and deposited, then concentrated in dry soils, and is possibly a minor component in the biogeochemical cycle of chlorine.

  15. The Two-stage Push Material Centrifuge In The Production Of Sodium Chlorate Application And Improvement%双级推料离心机在氯酸钠生产中的应用及改进

    Institute of Scientific and Technical Information of China (English)

    余浩; 崔政

    2011-01-01

    双级活塞推料离心机以其独有的自动连续操作、生产能力高、功率消耗低等优势,已被越来越多的氯酸盐生产企业认识和使用。针对双级推料离心机结构特点、氯酸钠物料特性及在氯酸钠脱水中存在的问题,提出了对双级推料离心机在结构及操作维护上的改进。%Two-stage push centrifuges with its unique automatic and continuous operation,high productive capacity,low power consumption advantages,has been more and more the chlorate production companies know and use.In view of the two-stage push material structure characteristics,sodium chlorate centrifuge material properties and the problem in sodium chlorate dehydration,it presents Two-stage pusher centrifuges in structure and operation and maintenance centrifuge on improvement.

  16. 离子膜电解盐水中氯酸盐含量的测定%Determination of chlorate content in brine for ion-exchange membrane electrolyzsis

    Institute of Scientific and Technical Information of China (English)

    李志平

    2015-01-01

    提出用双氧水测定离子膜法烧碱生产用的盐水中的氯酸盐含量。试验结果表明:采用该法检测,相对标准偏差低于0.4%,回收率在99%以上。%A method of using hydrogen peroxide to determine chlorate content in brine used for production of ion-exchange membrane caustic soda was proposed.Test results showed that relative standard deviation was lower than 0 .4%, and recovery rate was more than 99%.

  17. Development of Detection Method for Chlorates of Alkali Metals in Cosmetics%化妆品中碱金属氯酸盐的检测方法研究

    Institute of Scientific and Technical Information of China (English)

    杨轶眉; 李勤; 薛峰

    2014-01-01

    A thin layer chromatography(TCL)&potentiometric titration method was developed for the determination of chlo-rates of alkali metals in cosmetics. Chlorates were separated from other halates by thin layer chromatography and identified by the oxidation of iodide to form iodine. After identification,chlorate was reduced by zinc powder under acid conditions. The formed chloride was measured by potentiometric titration using a silver nitrate solution. The results showed that the recovery of the method was in the range of 81.4% to 105.2% under the concentration of 0.03% to 3.41% while being counted as chlorate ions(with relative standard deviation of not more than 10% ). Additionally,the detection and quantification limits were found to be 0.03% and 0.10% respectively.%建立了薄层色谱法和电位滴定法联用测定化妆品中碱金属氯酸盐含量的方法。用薄层色谱将氯酸盐从其他卤酸盐中分离,与碘化物形成碘来鉴别碱金属的氯酸盐。通过鉴别试验后,在酸性条件下氯酸盐被锌粉还原,所形成的氯化物用硝酸银溶液进行电位滴定。试验结果表明:在0.03%~3.41%(以氯酸根离子计)的质量分数范围内,加标回收率为81.4%~105.2%,相对标准偏差(RSD)≤10%;定性检出限为0.03%(质量分数),定量检出限为0.10%(质量分数)。

  18. Ion chromatographic determination of trace iodate, chlorite, chlorate, bromide, bromate and nitrite in drinking water using suppressed conductivity detection and visible detection.

    Science.gov (United States)

    Binghui, Zhu; Zhixiong, Zhong; Jing, Yao

    2006-06-16

    An ion chromatography method for the simultaneous determination of trace iodate, chlorite, chlorate, bromide, bromate and nitrite in drinking water has been developed using an anion-exchange column and the suppressed conductivity detector, followed by post-column addition of reagent to enhance visible absorbance detection of ions. A high capacity anion exchange Ion Pac9-HC column (250 mm x 4 mm I.D.) was used. Eight millimole per liter sodium carbonate was used as eluent, an auto-suppression external water mode was selected, 0.5 g/l o-dianisidine.2HCl (ODA)+4.5 g/l KBr+25% methanel+5.6% nitric acid was used as post-column reagent. The post-column reaction (PCR) temperature was at 60 degrees C, and the visible absorbance detected wavelength at 450 nm. The sample's pH and coexist anions had no influence on determination. The method enjoyed a wide linear range and a good linear correlation coefficient (r>0.999). The method detection limits were between 0.023 and 2.0 microg/l. The average recoveries ranged from 87.5 to 110.0%, and the relative standard deviations (RSD) were in the range of 1.1-4.6%. The analytical results by the method of post-column addition of reagent to enhance visible absorbance detection of anions was compared with that of the suppressed conductivity detection, and the former was proved to be better in sensitivity and selectivity. The results showed that this method was accurate, sensitive and might be good for application and suitable for trace analysis at the level of mug/l.

  19. Thermal Reactivity of Organic Molecules in the Presence of Chlorates and Perchlorates and the Quest for Organics on Mars with the SAM Experiment Onboard the Curiostiy Rover

    Science.gov (United States)

    Szopa, Cyril; Millan, Maeva; Buch, Arnaud; Belmahdi, Imene; Coll, Patrice; Glavin, Daniel P.; Freissinet, Caroline; Eigenbrode, Jennifer; archer, doug; sutter, brad; Summons, Roger; Navarro-Gonzalez, Rafael; Mahaffy, Paul; cabane, Michel

    2016-10-01

    One of the main objectives of the Sample Analysis at Mars (SAM) experiment is the in situ molecular analysis of gases evolving from solid samples collected by Curiosity when they are heated up to ~850°C. With this aim SAM uses a gas-chromatograph coupled to a mass spectrometer (GC-MS) able to detect and identify both inorganic and organic molecules released by the samples.During the pyrolysis, chemical reactions occur between oxychlorines, probably homogeneously distributed at Mars's surface, and organic compounds SAM seeks for. This was confirmed by the first chlorohydrocarbons (chloromethane and di- and trichloromethane) detected by SAM that were entirely attributed to reaction products occurring between these oxychlorines and organics from instrument background. But SAM also detected in the Sheepbed mudstone of Gale crater, chloroalkanes produced by reaction between oxychlorines and Mars indigenous organics, proving for the first time the presence of organics in the soil of Mars. However, the identification of the molecules at the origin of these chloroalkanes is much more difficult due to the complexity of the reactivity occurring during the sample pyrolysis. If a first study has already been done recently with this aim, it was relatively limited in terms of parameters investigated.This is the reason why, we performed a systematic study in the laboratory to help understanding the influence of oxychlorines on organic matter during pyrolysis. With this aim, different organic compounds from various chemical families (e.g. amino and carboxylic acids) mixed with different perchlorates and chlorates, in concentrations compatible with the Mars soil from estimations done with SAM measurements, were pyrolyzed under SAM like conditions. The products of reaction were analyzed and identified by GC-MS in order to show a possible correlation between them and the parent molecule. Different parameters were tested for the pyrolysis to evaluate their potential influence on the

  20. 氢氧化钠溶液中氯酸钠含量测定方法探究%Study on the content determination method of sodium chlorate in sodium hydroxide solution

    Institute of Scientific and Technical Information of China (English)

    李云枫; 王世荣

    2011-01-01

    对GB/T11200.1—89与GB/T11200.1—2006测定氢氧化钠溶液中氯酸钠含量的方法进行了分析,对GB/T11200.1—89测定氢氧化钠溶液中氯酸钠含量分析方法进行了实验研究,并提出了修改建议。%The content determination method of sodium chlorate in sodium hyd~vxide solution accrding to GB/T11200-89 and GB/T11200-2006 was studied by the experiment and analysis method. MoreoveL, some useful revisions were attempted, which make the content determin

  1. 饮用水中的亚氯酸盐、氯酸盐和溴酸盐的离子色谱测定法%Determination of Chlorite ,Chlorate and Bromate in Drinking Water by Ion Chromatography

    Institute of Scientific and Technical Information of China (English)

    周虹; 周小新

    2009-01-01

    Objective To develop an ion chromatography (IC) for simultaneous determination of chlorite, chlorate and bromate in drinking water. Methods The IC separation was carried out with the IonPAC AS23 column by using 4.5 mmol/L Na_2CO_3-0.8 mmol/L NaHCO_3 at the flow rate of 1.0 ml/min. The injection volume was 250 μl.the temperature of conductivity detector cell and column were 30 ℃ and 35 ℃, respectively. The pressure upon the bottle of mobile phase was 40 kPa. The current of auto-regenerating suppressor was 25 mA. Results The results showed that in the range of 0 to 1 000 mg/L, the calibration equation for chlorite was y=0.009 6+1.600 0 x (r=0.999 3),for bromate was y=0.003 2+3.184 7 x (r=0.999 9),for chlorate was y= 0.001 8+1.788 9 x(r=0.999 9).The detection limit of chlorite,chlorate and bromate were all 5 μg/ L,the recovery rates were 89.0% -108.0% and the relative standard deviations (RSD) were 0.21%-2.70%. Conclusion The method is simple,fast,accurate, sensitive, little interference and is applicable to the simultaneous determination of chlorite, chlorate and bromate in drinking water.%目的 建立同时测定饮用水中亚氯酸盐、氯酸盐和溴酸盐的离子色谱法.方法 选择IonPacAS23色谱柱,淋洗液为4.5mmol/L Na_2CO_3-0.8 mmol/L NaHCO_3,流速为1.0 ml/min,进样量为250 μl,电导检测池温度为30℃,色谱柱温度为35 ℃,流动相瓶加压为40 kPa,抑制器抑制模式为自动再生模式,抑制器电流为25 mA.结果 在0~1 000.0 mg/L范围内,亚氯酸盐的线性方程为:y=0.009 6+1.600 0x,r=0.999 3,检出限为5μg/L;溴酸盐的线性方程为:y=0.003 2+3.184 7x,r=0.999 9,检出限为5μg/L;氯酸盐的线性方程为:y=0.001 8+1.788 9x,r=0.999 9,检出限为5μg/L.加标回收试验结果显示,该方法的平均回收率为89.0%~108.0%,RSD为0.21%~2.70%.结论 该法操作简单、快速、准确,灵敏度高、干扰少,适用于饮用水中亚氯酸盐、氯酸盐和溴酸盐的同时测定.

  2. 生活饮用水中溴酸盐、氯酸盐和亚氯酸盐的离子色谱测定法%Determination of bromate, chlorate, and chlorite in drinking water by ion chromatography

    Institute of Scientific and Technical Information of China (English)

    孙卫明; 孙建飞; 王权帅

    2013-01-01

    [ Objective ] To establish a method for determination of bromate, chlorate, and chlorite in drinking water by ion chroma-tography. [ Methods] ] After filtration by 0.22 μm membrane filter, The water samples were put into the ion exchange system of ion chromatography, with the potassium hydroxide eluent. Different ions separated with the different affinity in one separation column and determined quantitatively by the external standard method. [ Results] Recoveries of bromate were 87.5% to 116.0% , and the relative standard deviation (RSD) was 69% ; recoveries of chlorate were 86. 8% to 99.0% , with RSD of 1. 21% ; recoveries of chlorite of 80.1% to 87.0% , with the RSD of 0.93% and the correlation coefficients of all 3 ions were r >0.999 0. [ Conclusion] This method is simple, rapid, can obtain satisfactory separation, with high sensitivity and precision. Also, the recovery meets the methodological requirements. Above all, this method is entirely suitable for the simultaneous determination of bromate, chlorate, and chlorite in drinking water.%目的 建立离子色谱法测定生活饮用水中有溴酸盐、氯酸盐、亚氯酸盐的检测方法.方法 水样经0.22 μm滤膜过滤后,随氢氧化钾淋洗液进入离子色谱的离子交换系统.根据分离柱对不同离子的亲和力不同进行分离,外标法定量.结果 溴酸盐回收率为87.5% ~ 116.0%,相对标准偏差为2.69%;氯酸盐回收率为86.8%~ 99.0%,相对标准偏差为1.21%;亚氯酸盐回收率为80.1% ~ 87.0%,相对标准偏差为0.93%.以上3个项目相关系数均大于0.999 0.结论 该方法检测速度快,样品处理简便,能获得满意的分离效果,具有较高的灵敏度和精密度,回收率也满足方法学要求,完全适合于生活饮用水中有溴酸盐、氯酸盐、亚氯酸盐的同时测定.

  3. Determination of Chlorite, Bromate, Chlorate in Surface Water and Drinking Water by Ion Chromatography%离子色谱法测定地表水和饮用水中亚氯酸盐、溴酸盐和氯酸盐

    Institute of Scientific and Technical Information of China (English)

    窦艳艳; 杨丽莉; 徐荣; 胡恩宇

    2013-01-01

    采用KOH梯度淋洗离子色谱法测定地表水和饮用水中ClO2-、BrO3-和ClO3-,在试验确定的条件下,3种离子与F-、Cl-、NO2-、NO3-、SO2-4、Br-、I-等7种离子分离度良好。 ClO2-、BrO3-、ClO3-在50.0μg/L~1000μg/L范围内线性良好,检出限分别为5.2μg/L、8.9μg/L、7.6μg/L,环境水样加标平行测定的RSD分别为2.1%~5.4%、4.1%~5.4%、2.5%~4.8%,两个质量浓度水平加标的平均回收率分别为93.7%~96.5%、90.3%~94.8%、98.7%~111%。%An ion chromatography method for determining chlorite , bromate and chlorate in surface water and drinking water was studied .The separation of the anions was achieved on an IonPac AS 19 Column with KOH as eluent, the chlorite, bromate, chlorate and other 7 kinds of anions could be well separated and determined within 25 min by employing a concentration gradient .The method has good linearity during the concentration 50.0 μg/L ~1 000 μg/L.The method detection limits of chlorite, bromate and chlorate was 5.2 μg/L, 8.9 μg/L and 7.6 μg/L, respectively.The RSD of the samples were 2.1%~5.4% ( chlorite), 4.1%~5.4%(bromate), and 2.5%~4.8% (chlorate).The recoveries of chlorite, bromate and chlorate in water samples were 93.7%~96.5%, 90.3%~94.8%and 98.7%~111%.

  4. 氯酸钠法制备二氧化氯还原剂研究进展%Research progress in reducing agent for preparation of chlorine dioxide by sodium chlorate process

    Institute of Scientific and Technical Information of China (English)

    李建生; 刘炳光; 孙宝丰; 董广前; 王芳

    2012-01-01

    对比介绍了氯酸钠法生产二氧化氯常用还原剂的特点;综述了氯酸钠法制备二氧化氯新还原剂(硫化合物、多元醇、有机酸、碳水化合物、尿素和乙二醛)的研究进展;讨论了氯酸钠法制备二氧化氯有机还原剂甲醇和乙二醛的作用机理;指出采用复合还原剂降低生产成本和采用有机还原剂同时制备两种有用产品是氯酸钠法制备二氧化氯还原剂发展趋势.%Characteristics of reducing agents commonly used in industrially producing chlorine dioxide were introduced with comparison.Research progress in new reducing agents,such as sulfur compound, poly alcohol, organic acid, carbohydrate, urea, and glyoxal for the preparation of chlorine dioxide by sodium chlorate process was summarized.Reaction mechanism of organic reducing agents, methanol and glyoxal, in preparation of chlorine dioxide was discussed.lt was pointed that decreasing production cost by using combined reducing agent as well as preparing two useful products simultaneously by using organic reducing agenl is the tendency of reducing agent development.

  5. Synthesis of CuO porous nanorods and their catalytic activity in the decomposition of potassium chlorate and peroxide%孔状氧化铜纳米棒的制备及其催化性能研究

    Institute of Scientific and Technical Information of China (English)

    徐惠; 黄剑; 陈泳

    2011-01-01

    Copper monoxide (CUO) porous nanorods of 100-200nm in diameter and 2-3μm in length were successfully synthesized using a hydrothermal reaction method in the presence of urea. The products were characterized by SEM., TEM, FT-IR, XRD and TG analysis techniques. The results of catalytic activity indicate that CuO nanocrystal promoted potassium chlorate and peroxide decomposition. When the ratio of H2O2 to CuP is 5 to 1,the decomposition of peroxide is perfect.%以硝酸铜为铜源,采用尿素矿化剂,通过水热法制得纳米氧化铜前驱体,高温煅烧后得到长21μm,直径200nm的氧化铜多孔纳米捧,所得产品尺寸均一,微孔分布均匀,排列整齐.通过IR、XRD、SEM以及TEM对其结构和形貌进行了表征.研究表明,所制备的纳米氧化铜多孔棒无需任何制样处理对氯酸钾和过氧化氢具有较高的催化活性,当n(H2O2):n(CuO)=5:1时,过氧化氢的分解速率最快.

  6. Spectrophotometric Determination of Nitrite by Catalytic Oxidation of Methyl Red with Potassium Chlorate%氯酸钾氧化甲基红催化光度法测定痕量亚硝酸根

    Institute of Scientific and Technical Information of China (English)

    李红艳; 李子荣

    2013-01-01

    This paper erects a new method for the storage of nitrite under normal temperature and pressure in brown volumetric flask storage by adding appropriate amount of sodium carbonate solution and sodium hydroxide.A method of measuring nitrite un-der the normal temperature and pressure is established.In the presence of nitrite, methyl red can be oxidized by potassium chlorate in the solution of H3 PO4 .Under the wavelength of maximum absorption 519nm and the conditions of the experiment, linear equa-tions: y =0.1443x +0.011, R =0.9990,linear range: 0.04 ~4.0 μg・ mL -1 , detection limit is 0.01μg・ mL -1 .The method is simple, fast, reproducible, energy saving and environmental protection,The method has been applied to the determination of boiling water, lake water and river water with satisfactory results.%  通过加入适量碳酸钠和氢氧化钠,用棕色容量瓶储藏,获得常温、常压下储存亚硝酸根的新方法。基于磷酸介质中,利用亚硝酸根对氯酸钾氧化甲基红褪色有诱导催化作用,建立了常温、常压下测定痕量亚硝酸根的方法,在最大吸收波长519 nm 及选择的试验条件下,线性方程 y =0.1463x +0.011,R =0.9990,线性范围0.04~4.0μg・ mL -1,检出限为0.01μg・ mL -1,该方法简单、快捷、重现性好,节能环保。

  7. Ion chromatography for simultaneous determination of bromate,chlorite and chlorate in drinking water%用离子色谱法同时测定生活饮水中溴酸盐、亚氯酸盐、氯酸盐

    Institute of Scientific and Technical Information of China (English)

    齐春华; 张颖; 王化勇

    2012-01-01

    Objective; To develop an ion chromatography (IC ) for simultaneous determination of chlorite, chlorate and bromate in drinking water. Methods: The IC separation was carried out with the IonPAC AS19 column by using hydroxide eluent at the flow rate of 1.0 ml/min. The injection volume was 500 jxl. Conductivity detection cell temperature was set at 30℃ , column temperature was set at 35℃. Suppressor was in automatic regeneration mode, suppressor current was 87 mA. Results: The results showed that in the range of 0 μg/L to 500 μg/L, the linear e-quation of chlorite was y =2. 640x -0.027, r =0.9999, the detection limit was 0. 1 μg/L; In the range of 0 μg/L ~ 100 μg/L, the linear equation of bromate was y = 1. 342x - 0. 003 , r - 0. 9999 , detection limit was 0. 5 μg/L; In the range of 0 μg/L -500 μg/L, the linear equation of chlorate was y =2. 157x -0. 043 , r -0. 9999, the detection limit was 0.2 μg/L. The recovery rates were 99. 70% ~102.6% and the relative standard deviations (RSD) were 1. 16% ~3.56%. Conclusion; The method is simple,fast,accurate, sensitive, little interference and applicable to the simultaneous determination of chlorite, chlorate and bromate in drinking water.%目的:建立能够同时测定生活饮用水中亚氯酸盐、氯酸盐和溴酸盐的离子色谱法.方法:选择Ion-PacAS19色谱柱,淋洗液为氢氧根淋洗液,流速为1.0 ml/min,进样量为500μl,电导检测池温度为30℃,色谱柱温度为35℃,抑制器抑制模式为自动再生模式,抑制器电流为87 mA.结果:在0μg/L ~ 500.0 μg/L范围内,亚氯酸盐的线性方程为:y=2.640x-0.027,r=0.9999,检出限为0.1 μg/L;在0μg/L ~ 100.0 μg/L溴酸盐的线性方程为:y=1.342x-0.003,r=0.9999,检出限为0.5 μg/L;在0μg/L~500.0 μg/L氯酸盐的线性方程为:y=2.157x-0.043,r=0.9999,检出限为0.2μg/L.加标回收试验结果显示,该方法的平均回收率为99.7% ~102.6%,RSD为1.16% ~3.56%.结论:该法操作简单、快速、准

  8. Simultaneous Determination of Trace Amount of Chlorite,Chlorate and Common Inorganic Anions in Running Water with kOH Isocratic Elution by Ion Chromatographic Method%KOH等度淋洗IC法同时测定自来水中微量ClO2-、ClO3-及常规阴离子

    Institute of Scientific and Technical Information of China (English)

    陈东; 罗倚坪

    2014-01-01

    The method to determine a trace of chlorite, chlorate and common inorganic anions in running water with KOH isocratic elution by ion chromatography was investigated. The conditions of method was that the concentration of KOH is 20. 5 mmol/L, the flow rate is 1. 0 mL/min, and the injection volume is 50 μL. The results showed that the concentration of F-,Cl-,NO3 -, SO4 2-,ClO2 -,ClO3 - in water was determined completely only in 12 minutes. The correlation coefficients of calibration curve was 0. 997 0-0. 999 9,while the detection limits was between 0. 05-7. 00 μg/L. The relative standard deviation( RSD) and the recoveries were between 0. 61%-3. 82%and 97. 6%-101. 7%, respectively. The method was sensitive, accurate and rapid, which was favorable to simultaneous quantification of chlorite, chlorate and common inorganic anions in drinking water.%建立了KOH等度淋洗离子色谱法同时测定自来水中微量亚氯酸盐、氯酸盐及氟化物、氯化物、硝酸盐、硫酸盐的分析方法。该方法以20.5 mmol/L KOH为淋洗液,流速1.0 mL/min,进样量50μL。结果表明,6种阴离子可在12分钟内检测完毕,各离子的线性相关系数为0.9970~0.9999;检出限为0.05~7.00μg/L;精密度为0.61%~3.82%;回收率为97.6%~101.7%,能够满足饮用水中这些指标的定量需要,是一种灵敏、准确、快速的理想方法。

  9. 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

  10. Microbial degradation of aliphatic and aromatic hydrocarbons with (per)chlorate as electron acceptor

    NARCIS (Netherlands)

    Mehboob, F.; Weelink, S.A.B.; Talarico Saia, F.; Junca, H.; Stams, A.J.M.; Schraa, G.

    2009-01-01

    "Water is life!" All active cellular systems require water as the medium and solvent of their metabolic activities. Hydrophobic compounds and structures, which tend to exclude water, though providing inter alia excellent sources of energy and a means of biological compartmentalization, present probl

  11. Optimization of chlorate decomposition system%氯酸盐分解系统的优化

    Institute of Scientific and Technical Information of China (English)

    周菊

    2014-01-01

    分析了离子膜烧碱工艺中氯酸盐产生的主要原因、氯酸盐分解装置使用的工艺流程和分解过程中的反应机理及去除方法,提出了运行和安装该装置时各工艺参数最优控制及装置的优化改造.

  12. Safety and efficacy of low-dose, subacute exposure of mature ewes to sodium chlorate

    Science.gov (United States)

    The objective was to determine the safety and efficacy of low-dose, subacute exposure of mature ewes to NaClO3 in the drinking water. Twenty-five ewes (BW = 62.5 ± 7.3 kg) were placed indoors in individual pens with ad libitum access to water and feed. After 7 d of adaptation, ewes were assigned ran...

  13. Controlled clinical evaluations of chlorine dioxide, chlorite and chlorate in man.

    OpenAIRE

    Lubbers, J R; Chauan, S; Bianchine, J. R.

    1982-01-01

    To assess the relative safety of chronically administered chlorine water disinfectants in man, a controlled study was undertaken. The clinical evaluation was conducted in the three phases common to investigational drug studies. Phase I, a rising dose tolerance investigation, examined the acute effects of progressively increasing single doses of chlorine disinfectants to normal healthy adult male volunteers. Phase II considered the impact on normal subjects of daily ingestion of the disinfecta...

  14. ESR of trapped centers in γ irradiated silver chlorates single crystals

    International Nuclear Information System (INIS)

    The paramagnetic centers O-3, ClO2, and (ClO2--Cl)- have been identified in irradiated AgClO3 single crystals by X and Q band ESR experiments at room temperatures and by the optical absorption bands at 480 and 360 nm, characteristic of the first two centers, respectively. The ESR spectrum and its angular dependence show that the first two centers have two magnetically inequivalent sites per unit cell. The third center was clearly observed only at certain orientations. The data for ClO2 show that the principal directions of the g and A tensors do not coincide; the two magnetically inequivalent sites have similar principal values of the g and A tensors related by a 900 rotation about the tetragonal crystal axis of symmetry, and can therefore be assumed to be chemically equivalent. It is found that the ClO2 center is formed substitutionally in the ClO-3 ion position, but that the ozonide O-3 is not. The thermal annealing of the γ irradiated AgClO3 has revealed an increase in the concentration of the O-3 radical that seems to be connected with the simultaneous destruction of the ClO2 center

  15. Ab initio investigations of the elastic properties of chlorates and perchlorates

    Science.gov (United States)

    Korabel'nikov, D. V.; Zhuravlev, Yu. N.

    2016-06-01

    Elastic properties of NaClO3, KClO3, LiClO4, NaClO4, and KClO4 have been investigated from first principles by the method of linear combination of atomic orbitals in the gradient approximation of the density functional theory using CRYSTAL software. The elastic constants and moduli, hardness, Poisson's ratio, and the anisotropy parameters have been calculated. The velocities of sound, the Debye temperature, the thermal conductivity, and the Grüneisen parameter have been estimated. It has been found that these compounds are mechanically stable, anisotropic, and ductile materials. The dependences of their elastic parameters on the atomic number of the cation have been calculated. The obtained results are in good agreement with the available experimental data.

  16. Microbial redox processes in deep subsurface environments and the potential application of (per)chlorate in oil reservoirs

    NARCIS (Netherlands)

    Liebensteiner, M.; Tsesmetzis, N.; Stams, A.J.M.; Lomans, B.P.

    2014-01-01

    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 m

  17. Les risques sanitaires des produits dérivés de la chloration des eaux de bassins de natation

    OpenAIRE

    Carbonnelle, Sylviane

    2003-01-01

    Les piscines sont fréquentées par de nombreuses personnes à travers le monde, pour y nager ou pour s’y délasser. Cependant, l’atmosphère chlorée des piscines pourrait être responsable de problèmes de santé. En effet, la majorité des piscines sont désinfectées par des produits à base de chlore –menant à la formation de dérivés potentiellement toxiques- et des études ont récemment attiré l'attention sur les risques pour la santé liés à la fréquentation des piscines. Il a entre autres été suggér...

  18. Sodium chlorate reduces presence of Escherichia coli in feces of lambs and ewes managed in shed-lambing systems

    Science.gov (United States)

    Our objective was to establish doses of orally-administered NaClO3 that reduced presence of generic Escherichia coli in intestines of ewes and neonatal lambs managed in a shed-lambing system. Neonatal lambs (n = 32; age = 7.1 ± 1.2 d; BW = 6.8 ± 1.0 kg) and yearling ewes (n = 44; BW = 74.8 ± 5.6 kg)...

  19. Discussion on the material of chlorate decomposition tank%氯酸盐分解槽材质的探讨

    Institute of Scientific and Technical Information of China (English)

    钱碧峰

    2005-01-01

    为寻求合适的氯酸盐分解槽材质,选取了金属钛、海特隆197玻璃钢、DERAKANE470玻璃钢3种材质进行腐蚀试验对比,结果认为:金属钛耐高温氯酸盐腐蚀,但价格昂贵;海特隆197玻璃钢性能不理想; DERAKANE470玻璃钢耐高温氯酸盐性能较理想,使用寿命、价格适中.

  20. Effect of the Presence of Chlorates and Perchlorates on the Pyrolysis of Organic Compounds: Implications for Measurements Done with the SAM Experiment Onboard the Curiosity Rover

    Science.gov (United States)

    Millan, M.; Szopa, C.; Buch, A.; Belmahdi, I.; Coll, P.; Glavin, D. P.; Freissinet, C.; Archer, P. D., Jr.; Sutter, B.; Summons, R. E.; Mahaffy, P.

    2016-01-01

    The Mars Science Laboratory (MSL) Curiosity Rover carries a suite of instruments, one of which is the Sample Analysis at Mars (SAM) experiment. SAM is devoted to the in situ molecular analysis of gases evolving from solid samples collected by Curiosity on Mars surface/sub-surface. Among its three analytical devices, SAM has a gaschromatograph coupled to a quadrupole mass spectrometer (GC-QMS). The GC-QMS is devoted to the separation and identification of organic and inorganic material. Before proceeding to the GC-QMS analysis, the solid sample collected by Curiosity is subjected to a thermal treatment thanks to the pyrolysis oven to release the volatiles into the gas processing system. Depending on the sample, a derivatization method by wet chemistry: MTBSTFA of TMAH can also be applied to analyze the most refractory compounds. The GC is able to separate the organic molecules which are then detected and identified by the QMS (Figure 1). For the second time after the Viking landers in 1976, SAM detected chlorinated organic compounds with the pyrolysis GC-QMS experiment. The detection of perchlorates salts (ClO4-) in soil at the Phoenix Landing site suggests that the chlorohydrocarbons detected could come from the reaction of organics with oxychlorines. Indeed, laboratory pyrolysis experiments have demonstrated that oxychlorines decomposed into molecular oxygen and volatile chlorine (HCl and/or Cl2) when heated which then react with the organic matter in the solid samples by oxidation and/or chlorination processes.

  1. 自冷结晶法在氯酸盐生产中的应用%Application of self-cooled crystallization process in production of chlorates

    Institute of Scientific and Technical Information of China (English)

    沈锡贤

    2002-01-01

    根据氯酸盐水溶液中氯酸钾溶解性的特点,提出在氯酸钠与氯化钾复分解反应生产氯酸钾过程中,采用自冷结晶的新方法.与传统的间歇冷却结晶法相比,该法具有避免产生晶垢、提高生产效率、节能和减轻劳动强度等优点.

  2. An analysis of relations for simultaneous production of after product of chlorate%浅析氯酸盐深加工产品的关联性

    Institute of Scientific and Technical Information of China (English)

    游立菡

    2003-01-01

    以氯酸钠为主产品,同时生产氯酸钾、高氯酸钾、亚氯酸钠、ADC发泡剂、合成盐酸6个深加工产品,研究了各产品之间的关联性,使物料最大限度地相互转化和平衡,从而确定最佳的规模匹配,使企业取得最佳的整体综合经济效益.

  3. Improvement on Chloration Synthesis Process of 2,4-Dichlorotoluene%2,4-二氯甲苯氯化合成工艺的改进

    Institute of Scientific and Technical Information of China (English)

    袁志明

    2003-01-01

    针对目前国内2,4-二氯甲苯生产合成工艺中存在的问题,改进了合成工艺,最佳工艺条件为反应温度40 ℃,转速30 r/min以及多管道通氯,使氯化收率提高至75%,氯气利用率提高至90%.

  4. Discussion on decomposition conditions of chlorate in brine by experiment%盐水中氯酸盐分解条件试验探讨

    Institute of Scientific and Technical Information of China (English)

    吴军祥; 王秀萍

    2011-01-01

    介绍了氯碱生产中电解盐水中氯酸盐的分解试验,并根据试验结果确定氯酸盐分解的最佳条件是:氢离子浓度0.8 - 1.0 mol/L、分解温度90 ~95℃、分解时间15 ~20min.

  5. Determination of chlorate and perchlorate in explosive residues of chlorate explosive by ion chromatography%离子色谱法检测氯酸盐炸药爆炸残留物中ClO-3和ClO-4

    Institute of Scientific and Technical Information of China (English)

    杨开莲

    2010-01-01

    利用离子色谱法检测氯酸盐类炸药爆炸残留物中的ClO-3和ClO-4,采用高容量阴离子分析柱IonPac AS23、抑制型电导检测,以KOH为流动相,等度淋洗.19 min内测定样品中包含ClO-3和ClO-4在内的4种阴离子,ClO-3和ClO-4的保留时间分别为5.0 min和17.7 min,检出限(S/N=3)分别为3.0 μg/L和5.0 μg/L.将此法应用于两起爆炸案的检材测定,4种阴离子的加标回收率在94.2%~101.1%之间.

  6. 氯酸盐在龙眼生产中运用和研究现状及其生物学效应的机理探讨%Current Situation in the Research and Application of Chlorate in Longan Production and Approaches to Understanding the Mechanisms of the Biological Effects of Chlorate

    Institute of Scientific and Technical Information of China (English)

    陆洁梅; 黄旭明; 王惠聪; 张承林; 杨瑞陶; 谢亮

    2006-01-01

    文章介绍了国内外利用氯酸钾诱导龙眼成花的现状和存在的问题,结合氯酸钾在其他生物中的生理学研究进展,探讨其对龙眼生物学效应的可能机理,并提出了进一步研究的设想.

  7. The Improvement of the Experiment Equipment of Potassium Chlorate and Manganese Dioxider for the Preparation of Oxygen%氯酸钾和二氧化锰制备氧气实验装置的改进

    Institute of Scientific and Technical Information of China (English)

    陈浩漫; 穆旗旗; 衷明华

    2015-01-01

    利用具支试管、橡胶管、直角导管、集气瓶、烧杯等常见实验仪器对氯酸钾和二氧化锰制备氧气的实验装置进行了改进,增强了实验的直观性和简易性,更加利于教师在课堂上演示实验.

  8. 氯酸钾氧化孔雀绿催化光度法测定痕量锇%CATALYTIC SPECTROPHOTOMETRIC DETERMINATION OF TRACE AMOUNTS OF OSMIUM ON OXIDATION OF MALACHITE GREEN BY USING POTASSIUM CHLORATE

    Institute of Scientific and Technical Information of China (English)

    唐宁莉; 黄尚格

    1999-01-01

    基于在稀硫酸溶液中,As(Ⅲ)存在下,Os(Ⅷ)对KClO3氧化孔雀绿的褪色反应具有强烈的催化作用,提出了催化光度法测定痕量锇的新方法,其灵敏度为4.98×10-13 g/L Os(Ⅷ),测定范围为0~6 ng/12 mL,用于地质管理样中痕量锇的测定.

  9. A Preliminary Investigation of the Influences of the Application of Potassium Chlorate on the Flower Forming of Longan%施用氯酸钾对龙眼成花影响初探

    Institute of Scientific and Technical Information of China (English)

    李莲英

    2002-01-01

    @@ 九十年代中后期台湾、泰国已有反季节龙眼批量出口,倍受瞩目的龙眼药物催花技术又称龙眼产期调控或反季节栽培,目前在龙眼促花方面取得一定的成效.

  10. Determination of Chlorine Dioxide, Chlorine, Chlorite and Chlorate in Water by Ion Chromatography%用离子色谱法测定水中的二氧化氯、氯、亚氯酸根及氯酸根

    Institute of Scientific and Technical Information of China (English)

    田芳; 谢家理

    2004-01-01

    建立了一种测定水中的ClO2、Cl2、ClO-2、ClO-3离子色谱法,在含有碳酸氢钠缓冲溶液的中性条件下,用NaNO2将ClO2、Cl2还原为ClO-2、Cl-,通过测定ClO-2和NO-3的变化值,间接测定ClO2和Cl2.加入硫代乙酰胺(TAA)作掩蔽剂测定ClO-2.

  11. 再论氯酸钾与花炮安全生产的关系%Discussion on the Relationship of Potassium Chlorate with Safety in Production of Fireworks

    Institute of Scientific and Technical Information of China (English)

    刘青春

    2002-01-01

    根据硫磺对感度的贡献明显大于氯酸钾的实验事实,参照部分国家有关花炮条例和标准,提出我国花炮生产除已规定的"硫化锑不得与氯酸盐配伍"外,应补充规定"硫磺不得与氯酸盐配伍",以应对WTO规则,确保烟花炮竹安全生产.

  12. Study of 10 Metal Oxides on the Thermal Decomposition of Potassium Chlorate to Yield Oxygen%10种金属氧化物对氯酸钾热分解制氧催化效果的研究

    Institute of Scientific and Technical Information of China (English)

    陈金娥; 张海容

    2001-01-01

    加热KCIO3分解制氧常使用MnO2作催化剂.实验发现:CaO,Al2O3,CuO,Fe2O3,TiO2,Nd2O3,PdO2,V2O5,Cr2O3 9种金属氧化物及无机盐MnSO4,FeCl2,FeCl3,CoCl2,ZnCl2等亦有较好的催化效果,在试剂用量、产氧量、反应速度和控制副反应等方面具有明显的优点.

  13. COMPARATIVE STUDY OF CHLORATED AND PHOSPHORATED INSECTICIDES IN BAIT ATTRACTIVENESS BY “BANANA BORER” (Cosmopolites sordidus GERMAR, 1824 ESTUDO COMPARATIVO DE INSETICIDAS CLORADOS E FOSFORADOS NA ATRATIVIDADE DE ISCAS PELO “MOLEQUE DA BANANEIRA” (Cosmopolites sordidus Germar, 1824

    Directory of Open Access Journals (Sweden)

    Ronaldo Veloso Naves

    2007-09-01

    Full Text Available

    The efficiency of several insecticides for the control of the banana borer were tested in two kinds of traps. The cloride insecticides are most widely used but they are probably repellent to the weevil. DDT, Aldrin, Diazinon and Parathion were compared in two kinds of traps: slices of rhizome and pieces of pseudostem. The best results were obtained with Parathion in rhizome slices.

    A broca-da-bananeira ou “moleque” (Cosmopolites sordidus Germar é urna das pragas mais importantes da bananeira. A revisão de literatura mostra que os produtos clorados são os mais utilizados e recomendados no combate a essa praga, principalmente, Aldrin. O presente trabalho visou a testar inseticidas fosforados e também verificar o tipo de isca mais atrativa. A análise estatística dos dados obtidos demonstrou haver diferença significativa entre os tratamentos, entre os dois tipos de iscas, e na interação iscas x tratamento. Com base nos resultados e observações feitas durante a fase experimental, podemos tirar as seguintes conclusões: a As iscas do tipo sanduíche, feitas com pedaços de rizoma são mais atrativas do que as do tipo telha, feita de pedaços de pseudo-caule, cortados longitudinalmente; b O inseticida que apresentou melhores resultados foi o RHODIATOX (Parathion.

  14. Chloriet, chloraat en bromaat in drink- en oppervlaktewater: Voorkomen, herkomst en gezondheidsaspecten

    NARCIS (Netherlands)

    Versteegh JFM; Neele J; Cleven RFMJ

    1992-01-01

    Chlorate and chlorite exist in surface water especially in the rivers Meuse and Rhine. The average concentration of chlorite and chlorate in river water varies from 10 - 40 mug/l during the six months monitoring program in 1991/1992. The concentrations are lowered during dune infiltration and afte

  15. Arabidopsis CDS blastp result: AK287911 [KOME

    Lifescience Database Archive (English)

    Full Text Available AK287911 J065213B08 At1g12110.1 68414.m01402 nitrate/chlorate transporter (NRT1.1) ...(CHL1) identical to nitrate/chlorate transporter SP:Q05085 from [Arabidopsis thaliana]; contains Pfam profile: PF00854 POT family 3e-85 ...

  16. Arabidopsis CDS blastp result: AK318551 [KOME

    Lifescience Database Archive (English)

    Full Text Available AK318551 J075138M12 At1g12110.1 68414.m01402 nitrate/chlorate transporter (NRT1.1) ...(CHL1) identical to nitrate/chlorate transporter SP:Q05085 from [Arabidopsis thaliana]; contains Pfam profile: PF00854 POT family 4e-27 ...

  17. Arabidopsis CDS blastp result: AK241823 [KOME

    Lifescience Database Archive (English)

    Full Text Available AK241823 J065212G21 At1g12110.1 68414.m01402 nitrate/chlorate transporter (NRT1.1) ...(CHL1) identical to nitrate/chlorate transporter SP:Q05085 from [Arabidopsis thaliana]; contains Pfam profile: PF00854 POT family 1e-150 ...

  18. Arabidopsis CDS blastp result: AK243378 [KOME

    Lifescience Database Archive (English)

    Full Text Available AK243378 J100063A13 At1g12110.1 68414.m01402 nitrate/chlorate transporter (NRT1.1) ...(CHL1) identical to nitrate/chlorate transporter SP:Q05085 from [Arabidopsis thaliana]; contains Pfam profile: PF00854 POT family 5e-18 ...

  19. Arabidopsis CDS blastp result: AK288351 [KOME

    Lifescience Database Archive (English)

    Full Text Available AK288351 J090024C17 At1g12110.1 68414.m01402 nitrate/chlorate transporter (NRT1.1) ...(CHL1) identical to nitrate/chlorate transporter SP:Q05085 from [Arabidopsis thaliana]; contains Pfam profile: PF00854 POT family 2e-24 ...

  20. Copper and silver halates

    CERN Document Server

    Woolley, EM; Salomon, M

    2013-01-01

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

  1. Arabidopsis CDS blastp result: AK242252 [KOME

    Lifescience Database Archive (English)

    Full Text Available AK242252 J075182G16 At1g12110.1 68414.m01402 nitrate/chlorate transporter (NRT1.1) ...(CHL1) identical to nitrate/chlorate transporter SP:Q05085 from [Arabidopsis thaliana]; contains Pfam profile: PF00854 POT family 6e-88 ...

  2. Chlorine dioxide and by-products in water distribution systems

    OpenAIRE

    Ferreira, Francisco Cardoso

    1991-01-01

    Chlorine dioxide is used as both a pre-oxidant and/or a post-disinfectant in several water treatment plants in the United States. Chlorine dioxide is associated with its byproducts chlorite and chlorate. Chlorine dioxide, chlorine, chlori te and chlorate were sampled in four distribution systems where chlorine dioxide is used for disinfection purposes: Charleston, WV, Columbus, GA, New Castle, PA, and Skagit, WA. The fate of chlorine dioxide and its by-products in dist...

  3. Chlorine dioxide by-products in drinking water and their control by powdered activated carbon

    OpenAIRE

    Grabeel, Margaret N.

    1992-01-01

    The concentrations of chlorine dioxide (CI02), chlorine, chlorite (CIO2), and chlorate (CI03) were evaluated following pretreatment of raw water by CI02 at water treatment plants in New Castle, Pennsylvania; Charleston, West Virginia; Skagit, Washington; and Columbus, Georgia. Chlorite and chlorate concentrations were unaffected by any of the water treatment processes and did not vary as a function of time of travel in the distribution system. Chlorine dioxide, which was ana...

  4. Study and application of sodium chlorate oxygen equipment on safety protection of pipeline construction in trench%氯酸钠氧烛装置在管道沟下作业安全防护中的应用研究

    Institute of Scientific and Technical Information of China (English)

    王江宇; 齐晨光; 汪振宇

    2016-01-01

    管道施工人员在沟下作业时,时常面临着管沟塌方,人员被土体掩埋的风险,现实中发生的多起事故均反映出缺氧窒息是被掩埋人员死亡的主要原因.为了保证遇险工人的安全,为沟下作业的工人装备氯酸钠氧烛,一旦管沟塌方将人员掩埋,遇险人员可立即启动氧烛装置,在一定时间内维持被埋状态下的氧气供应,保证人的呼吸,从而为营救行动争取宝贵时间,最大限度避免人员伤亡事故.

  5. Catalytic kinetic spectrophotometric determination of trace copper using copper(Ⅱ)-potassium chlorate-phenylhydrazine hydrochloride-α-naphthylamine system%铜(Ⅱ)-氯酸钾-盐酸苯肼-α-萘胺体系催化动力学光度法测定痕量铜

    Institute of Scientific and Technical Information of China (English)

    任健敏; 林壮森; 彭珊珊

    2006-01-01

    基于铜(Ⅱ)催化氯酸钾氧化盐酸苯肼继而与α-萘胺偶合显色的反应,建立了催化动力学光度法测定痕量铜的新方法.通过正交试验得到测定痕量铜的最佳条件.在合适条件下,催化和非催化反应吸光度差(△A)与反应时间(t)呈线性关系,其回归方程为△A=2.857 1+55.087t,r=0.998 5;表观速率常数为k=8.2×10-2/s,为准零级反应;表观活化能为92.1kJ/mol,方法的线性范围为0~0.08μg/mL,检出限为6.26×10-10 g/mL.大多数离子无干扰,Fe3+干扰可加入NaF掩蔽.用于管网水中痕量铜的测定,回收率96.8%和98.8%.

  6. The Effect of the Compounds of Rare Earths Chlorate (Pr,Nd) on Tissue Culture and Rapid Propagation of Saintpaulia Ionantha Wendl%稀土(镨、钕)配合物对非洲紫罗兰组织培养与快繁的影响

    Institute of Scientific and Technical Information of China (English)

    王艳; 杨一心; 聂光华; 但悠梦

    2005-01-01

    测定了两种氯稀土与乙酰丙氨酸咪唑配合物RE(C5H8NO3)2(C3H5N2)2Cl3·4H2O(RE=Pr、Nd)对非洲紫罗兰组织培养及快繁的影响,结果表明:稀土配合物对非洲紫罗兰组织培养及快繁确有一定的促进作用,但其范围有限,浓度太高将抑制外植物的生长.低于800mg/L浓度的稀土配合物一般可以使植物正常生长或不同程度的有促进作用,且不同稀土之间也有差异.

  7. Studies of nitrate transport by marine phytoplankton using TWCl-ClO3 as a transport analogue. I. Physiological findings. [Skeletonema costatum; Nitzschia closterium

    Energy Technology Data Exchange (ETDEWEB)

    Balch, W.M.

    1987-03-01

    Transport of a nitrate analogue, TWCl-ClO3 , was examined in two diatoms, Skeletonema costatum (Greve.) Cleve and Nitzschia closterium (Ehrenb) W. Sm. A dinoflagellate, Gonyaulax polyedra did not transport ClO3 . Transport of TWCl-ClO3 by diatoms appeared to be active and showed saturation kinetics. The data were fitted by Michaelis-Menten equation at all but the lowest chlorate concentrations (where plots of S vs. v showed a slight concave bend). Affinity of cells for nitrate was considerably higher than for chlorate. The K/sub i/ for nitrate inhibition of chlorate transport was calculated assuming competitive inhibition. Light had little or no effect on chlorate transport. Pulse-chase experiments demonstrated that (1) ClO3 (hence NO3 ) was stored in two intracellular compartments of equal size, (2) internal ClO3 was exchangeable with external ClO3 (rates of efflux and influx were measured), and (3) efflux of intracellular ClO3 showed transient states following a chase of ClO3 or NO3 which stabilized after 10-20 min. Transport of chlorate was a function of growth phase.

  8. The tropical fruit and nut collections and research activities at the USDA-ARS Pacific Basin Agricultural Research Center, Tropical Plant Genetic Resource and Disease Research unit

    Science.gov (United States)

    In Hawaii, consistency and reliability are important factors determining the success of a crop, for example, longan generated the highest income return for the farmers among the Sapindaceae (lychee, longan and rambutan) group in 2006 because of the use of potassium chlorate for off-season production...

  9. Chloroxyanion residues in cantaloupe and tomatoes after chlorine dioxide gas sanitation

    Science.gov (United States)

    Chlorine dioxide gas is effective at cleansing fruits and vegetables of bacterial pathogens and(or) rot organisms, but few data are available on chemical residues remaining subsequent to chlorine gas treatment. Therefore, studies were conducted to quantify chlorate and perchlorate residues after tom...

  10. Food safety on the farm: Movement toward the development of sustainable and environmentally compatible pre-harvest interventions for livestock producers

    Science.gov (United States)

    Pathogenic bacteria residing in the gut of food-producing animals can contaminate meat and dairy products during processing. A chlorate-based feeding strategy specifically targeting respiratory nitrate reductases possessed by E. coli and Salmonella has shown promise in depopulating these pathogens. ...

  11. New Rice Mutants(NR676 and NR827)Low in Nitrate Reduction

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Mutants deficient in nitrate reductase(NR) were classfied into two groups,nia types are deficient in apoprotein and cnx types are lack of Mo- Co. This paper reports the characteristics of low NR mutants,which are not deficient in NR activity but 40%~60% of the NR activity of the wild type,Nipponbare. Mutants NR676 and NR827 were selected as seedings showing poor growth with nitrate as sole mitrogen source from M2 population. They exhibited chlorate resistance. Genetic analysis in the F1 and F2 indicated that chlorate resistance in the mutants was transmitted by a single recessive nuclear gene and that NR676 and NR827 were induced by a mutation at a single locus. In the F2 population,all of the seedings showing yellow green leaves were resistant to chlorate and low in NR activity. Photosynthetic rate and mRNA expression of NR676 and NR827 were lower than wild type. These results suggested that low NR activity and chlorate resistance of NR676 and NR827 were caused by a defect in photosynthetic process.

  12. 40 CFR Table 10 to Part 455 - List of Appropriate Pollution Control Technologies

    Science.gov (United States)

    2010-07-01

    .... Boron sodium oxide (B4Na2O7) (1330-43-4) 11112 Inorganic Pollution Prevention. Polybutene 11402 Polymer...-polymer 72701 Polymer Activated Carbon. Sodium chlorate 73301 Inorganic Pollution Prevention. Calcium... 40 Protection of Environment 29 2010-07-01 2010-07-01 false List of Appropriate Pollution...

  13. 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.

  14. 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

  15. Chlorine dioxine DBPs (disinfection by-products in drinking water

    Directory of Open Access Journals (Sweden)

    C. Lasagna

    2013-01-01

    Full Text Available Since the 1970s it has been well known that, though water for human consumption is generally disinfected before being distributed along the network, the use of chemicals results in the formation of many different Disinfection By-Products (DBPs. In the case of chlorine dioxide, the most important and represented DBPs are chlorite and chlorate: after an introduction concerning the current Italian regulation on this subject, in the experimental part the results of a 7-year minitoring campaign, concerning water of different origin collected from taps in various Italian regions, are shown. The analytical technique used for the determination of chlorite and chlorate was Ion Chromatography. The result obtained are finally discussed.

  16. Recovery and Biological Properties of Nitrate Non-utilizing Mutants of Rice Blast, Magnaporthe grisea

    Institute of Scientific and Technical Information of China (English)

    ZHANG Chuan-qing; ZHOU Ming-guo

    2004-01-01

    Eleven nitrate non-utilizing (nit) mutants were recovered from six isolates of Magnaporthe grisea cultured on MM media amended with 60 g/L potassium chlorate, with a frequency of 1.42 %. Some biological properties, such as growth rate, growth biomass, cultural characters, conidial production, sexual reproduction ability, and pathogenicity were compared between nit mutants and their parent isolates. Results showed that all the nit mutants were resistant to chlorate. Some important biological properties such as the growth rate on YPSA, conidial production ability on TPSA, pathogenicity, had no significant differences between nit mutants and their parent isolates. Mating type didn't change, but perithecia production ability of fertile isolates changed significantly as compared with that of their parent isolates. Therefore, the nit can be used as a genetic marker to study the genetics such as pathogenicity, fungicide resistance in Magnaporthe grisea.

  17. 钛基二氧化铅阳极电化合成高氯酸钠的研究%ELECTROLYTIC SYNTHESIS OF SODIUM PERCHLORATE BY LEAD DIOXIDE ANODE BASED TITANIUM METAL

    Institute of Scientific and Technical Information of China (English)

    孙洋洲; 姚沛

    2001-01-01

    介绍了以钛基体二氧化铅作为阳极,电解氯酸钠合成高氯酸钠的过程。考察了电解温度、电解液初始氯酸钠浓度及氯化钠浓度对电流效率的影响。得出了电解反应的最佳条件。%A process of electrolytic synthesis of sodium perchlorate from sodium chlorate solution by lead dioxide anode based titanium metal is introduced. The influence of temperature,the concentration of sodium chlorate and the concentration of sodium chloride on the current efficiency is investigated, and the optimum conditions of the electrolytic process are also obtained.

  18. Measurement of temperature and temperature gradient in millimeter samples by chlorine NQR

    Science.gov (United States)

    Lužnik, Janko; Pirnat, Janez; Trontelj, Zvonko

    2009-09-01

    A mini-thermometer based on the 35Cl nuclear quadrupole resonance (NQR) frequency temperature dependence in the chlorates KClO3 and NaClO3 was built and successfully tested by measuring temperature and temperature gradient at 77 K and higher in about 100 mm3 active volume of a mini Joule-Thomson refrigerator. In the design of the tank-circuit coil, an array of small coils connected in series enabled us (a) to achieve a suitable ratio of inductance to capacity in the NQR spectrometer input tank circuit, (b) to use a single crystal of KClO3 or NaClO3 (of 1-2 mm3 size) in one coil as a mini-thermometer with a resolution of 0.03 K and (c) to construct a system for measuring temperature gradients when the spatial coordinates of each chlorate single crystal within an individual coil are known.

  19. New considerations on hydrogen peroxide and related substances as food additives in view of carcinogenicity.

    Science.gov (United States)

    Ito, R

    1982-01-01

    The use of hydrogen peroxide as a labile and safe food preservative in fish cake and boiled noodles has recently been restricted by the Japanese government, since hyperplasia has been found in the duodenum of mice after long-term peroral study. The action of compounds with resembling mode of action, potassium bromate as an improving agent in bread, and sodium chlorate as a weed killer are discussed in this paper in view of developmental and environmental pharmacology. PMID:7078983

  20. Disinfecting capabilities of oxychlorine compounds.

    OpenAIRE

    Noss, C I; Olivieri, V P

    1985-01-01

    The bacterial virus f2 was inactivated by chlorine dioxide at acidic, neutral, and alkaline pH values. The rate of inactivation increased with increasing pH. Chlorine dioxide disproportionation products, chlorite and chlorate, were not active disinfectants. As chlorine dioxide solutions were degraded under alkaline conditions, they displayed reduced viricidal effectiveness, thereby confirming the chlorine dioxide free radical as the active disinfecting species.

  1. Electrochemical and Integrated Process Opportunities for On-Site/On-Demand Generation of Chlorine Dioxide - Final Report - 08/02/1996 - 08/01/1999; FINAL

    International Nuclear Information System (INIS)

    Due to continued evidence of environmental harm from elemental chlorine bleaching, the nation's paper industry continues to search for cost effective alternative bleaching. A practical and cost effective bleaching alternative is chlorine dioxide manufactured entirely from sodium chlorate. Sodium chlorate is produced by the electrolysis of brine in an undivided cell with steel plate cathodes and dimensionally stable anodes. Although the overpotential at the anode is only 50 mV, the cathodic overpotential is 940 mV. Thus, nearly one volt of electricity is wasted in driving hydrogen evolution at the cathode. Auburn University's Center for Microfibrous Materials Manufacturing has demonstrated that high performance, three dimensional, microfibrous electrodes can improve the performance of capacitors, batteries, hybrid power cells, and electrolysis electrodes in a variety of applications. The goal of this research was to apply this technology to a chlorate cell's cathode and reduce the overpotential between 200 and 400 mV. An economic analysis of the industry has shown that for every 100 mV reduction in overpotential,$100 per square meter of electrode can be saved annually. Due to their enhanced surface area over plates, corrosion of microfibrous electrodes is a major issue in this research. Samples based on chromium protection (i.e. stainless steel) have proved unfeasible for chlorate application. However, samples based on stainless steel and nickel show dramatic performance improvements over industry status quo in chlor-alkali application. Building microfibrous electrodes on a titanium base protected with a silver coating alleviates the corrosion problem and provides 100 mV or more of overpotential reduction. Further reduction is realized by impregnating silver-titanium microfibrous mesh with a PVDF binder and dispersed platinum on activated carbon. The resulting electrodes are mechanically sound, active towards hydrogen evolution, and hold promise for practical

  2. Removal of chlorite by reaction with ferrous iron

    OpenAIRE

    Iatrou, Angela

    1991-01-01

    The use of chlorine dioxide as an oxidant and/or disinfectant for drinking water treatment has been an alternative considered when utilities seek to control trihalomethane concentrations. However, concern regarding residual concentrations of chlorite and chlorate have resulted in limitations on applied chlorine dioxide dosages. This study describes the use of ferrous iron as a possible reducing agent for the elimination of residual chlorite from drinking water.

  3. Electrochemical and Integrated Process Opportunities for On-Site/On-Demand Generation of Chlorine Dioxide - Final Report - 08/02/1996 - 08/01/1999

    Energy Technology Data Exchange (ETDEWEB)

    Tatarchuk, Bruce J.; Krishnagopalan, G.; Nickell, Ryan A.

    2000-01-30

    Due to continued evidence of environmental harm from elemental chlorine bleaching, the nation's paper industry continues to search for cost effective alternative bleaching. A practical and cost effective bleaching alternative is chlorine dioxide manufactured entirely from sodium chlorate. Sodium chlorate is produced by the electrolysis of brine in an undivided cell with steel plate cathodes and dimensionally stable anodes. Although the overpotential at the anode is only 50 mV, the cathodic overpotential is 940 mV. Thus, nearly one volt of electricity is wasted in driving hydrogen evolution at the cathode. Auburn University's Center for Microfibrous Materials Manufacturing has demonstrated that high performance, three dimensional, microfibrous electrodes can improve the performance of capacitors, batteries, hybrid power cells, and electrolysis electrodes in a variety of applications. The goal of this research was to apply this technology to a chlorate cell's cathode and reduce the overpotential between 200 and 400 mV. An economic analysis of the industry has shown that for every 100 mV reduction in overpotential, $100 per square meter of electrode can be saved annually. Due to their enhanced surface area over plates, corrosion of microfibrous electrodes is a major issue in this research. Samples based on chromium protection (i.e. stainless steel) have proved unfeasible for chlorate application. However, samples based on stainless steel and nickel show dramatic performance improvements over industry status quo in chlor-alkali application. Building microfibrous electrodes on a titanium base protected with a silver coating alleviates the corrosion problem and provides 100 mV or more of overpotential reduction. Further reduction is realized by impregnating silver-titanium microfibrous mesh with a PVDF binder and dispersed platinum on activated carbon. The resulting electrodes are mechanically sound, active towards hydrogen evolution, and hold promise for

  4. Mutagenesis and transformation of Aspergillus terreus based on the nitrate reductase pathway

    OpenAIRE

    Ferraz, Elza; Lima, Nelson; Mota, M

    1996-01-01

    Aspergillus terreus is an efficient producer of different extracellular enzymes which are used in food industries. Thus, we are interested in developing a genetic transformation system based on the nitrate structural gene niaD. In order to develop this system the nitrate assimilation pathway in A. terreus was studied and spontaneous mutants defective in the genes required for nitrate assimilation were obtained on the basis of chlorate resistance. Of particular interest were ...

  5. Kinetics and mechanism study on chlorine dioxide generation with hydrogen peroxide%过氧化氢法制备二氧化氯反应动力学及机理研究

    Institute of Scientific and Technical Information of China (English)

    朱明新; 黄辉; 董娴; 沈丽娜; 徐炎华

    2011-01-01

    The reaction between hydrogen peroxide and sodium chlorate in presence of aqueous sulfuric acid was studied at various temperatures and molar concentrations of hydrogen peroxide, chlorate and sulfuric acid. The reaction rate law was established by analyzing the consumption of chlorate or hydrogen peroxide. Reaction order is found 0. 5 and 1 with respect to hydrogen peroxide and chlorate concentration, respectively. Reaction order is found about 5. 99 with respect to molar concentration of sulfuric acid, but it reduces to 1. 64 when acidity func-tion(h- ) , is substituted in place of molar concentration. The reaction is a process of leat absorption and the activation energy is about 105kJ/mol. Reaction mechanism shows it is a self-catalyze reaction.%通过改变反应温度和物料浓度,研究过氧化氢与氯酸钠在硫酸溶液中的反应过程,获得宏观反应动力学方程,并对其反应机理进行了深入探讨.研究表明过氧化氢法制备二氧化氯反应过程中过氧化氢的反应级数为0.5,氯酸钠为1,对于硫酸摩尔浓度的反应级数为5.99,当用酸度函数(h_)代替硫酸摩尔浓度时反应级数则下降为1.64;该反应是吸热过程,反应活化能约为105kJ/mol;机理分析表明该反应是自催化反应过程.

  6. Disinfection aboard cruise liners and naval units: formation of disinfection by-products using chlorine dioxide in different qualities of drinking water.

    Science.gov (United States)

    Ufermann, Petra; Petersen, Hauke; Exner, Martin

    2011-12-01

    The world-wide deployment of cruise liners and naval units has caused an increased need for the disinfection of drinking water. The main cause for this is the unknown quality of drinking water in foreign harbours--besides the formation of bio-films due to the climatically disadvantageous conditions in the operational area. Water conduits on board are currently disinfected with calcium hypochlorite in case of microbiological contamination. Chemical and physical analyses after disinfection with calcium hypochlorite have shown that organic by-products consisting of trihalomethanes develop in considerable amounts during disinfection. Furthermore, the method is susceptible to handling errors and thus often leads to insufficient disinfection results. Hitherto, the use of other disinfection methods allowed by government regulations, especially chlorine dioxide, is not widely spread. Unlike disinfection with calcium hypochlorite, chlorine dioxide does not lead to the formation of trihalomethanes. Typical disinfection by-products (DBP) are the anions chlorite and chlorate, which are formed in oxidative processes. The formation conditions of these anions have not yet been elucidated. For this reason, the probability of the generation of inorganic by-products after disinfection with chlorine dioxide has been determined, and their occurrence in drinking water on board has been examined with respect to a possible correlation between water quality and the formation of chlorate and chlorite. Therefore, a chromatographic method was developed and validated in order to determine the periodical development of chlorate and chlorite from chorine dioxide in purified water at different pH-values as well as in actual drinking water samples from water conduits on board. The formation of the by-products chlorite and chlorate after disinfection with chlorine dioxide is influenced neither by pH-value nor by chemical properties of the disinfected water. Considering the examined conditions

  7. Nitrate Uptake into Barley (Hordeum vulgare) Plants 1

    Science.gov (United States)

    Deane-Drummond, Celia E.; Glass, Anthony D. M.

    1982-01-01

    Evidence is presented that chlorate is an extremely good analog for nitrate during nitrate uptake by intact barley (Hordeum vulgare cv. Fergus) roots. The depletion of ClO3− or NO3− from uptake media over 2 to 6 hours by seedlings was found to be dependent on combined NO3− plus ClO3− concentrations, and total anion uptake was equivalent at different NO3−/ClO3− ratios. After loading barley seedlings with 36ClO3− for 6 hours, kinetic parameters were derived from the analysis of efflux of [36Cl] chlorate into unlabeled solution. On the basis of this analysis, the half times for exchange for the cytoplasmic and vacuolar phases were 17 minutes and 20 hours, respectively. Data pooled from a number of different experiments were used to calculate kinetic constants (Km and Vmax) for 36ClO3− influx into barley roots at different external ClO3−/NO3− ratios, using short (10 minutes) influx times. There appeared to be no discrimination by the root cells between ClO3− and NO3−. Lineweaver-Burk analysis of the interaction between nitrate and chlorate were characteristic of competitive inhibition at low nitrate concentrations (0-0.5 mm). At higher concentrations, in the range of >1 mm, similar interactions between these ions were evident. PMID:16662478

  8. Genome analysis and physiological comparison of Alicycliphilus denitrificans strains BC and K601T

    Energy Technology Data Exchange (ETDEWEB)

    Oosterkamp, Margreet J. [Wageningen University and Research Centre, The Netherlands; Veuskens, Teun [Wageningen University and Research Centre, The Netherlands; Saia, Flavia Talarico [Wageningen University and Research Centre, The Netherlands; Weelink, Sander A.B. [Wageningen University and Research Centre, The Netherlands; Goodwin, Lynne A. [Los Alamos National Laboratory (LANL); Daligault, Hajnalka E. [Los Alamos National Laboratory (LANL); Bruce, David [Los Alamos National Laboratory (LANL); Detter, J. Chris [U.S. Department of Energy, Joint Genome Institute; Tapia, Roxanne [Los Alamos National Laboratory (LANL); Han, Cliff [Los Alamos National Laboratory (LANL); Land, Miriam L [ORNL; Hauser, Loren John [ORNL; Langenhoff, A. M. [Deltares, The Netherlands; Gerritse, Jan [Deltares, The Netherlands; Van Berkel, Willem J. H. [Wageningen University and Research Centre, The Netherlands; Pieper, Dietmar [HZI - Helmholtz Centre for Infection Research, Braunschweig, Germany; Junca, Howard [CorpoGen, Bogota Colombia; Smidt, Hauke [Wageningen University and Research Centre, The Netherlands; Schraa, Gosse [Wageningen University and Research Centre, The Netherlands; Davids, Mark [Wageningen University and Research Centre, The Netherlands; Schaap, Peter J [Wageningen University and Research Centre, The Netherlands; Plugge, Caroline M. [Wageningen University and Research Centre, The Netherlands; Stams, Alfons J. M. [Wageningen University and Research Centre, The Netherlands

    2013-01-01

    The genomes of the Betaproteobacteria Alicycliphilus denitrificans strains BC and K601T have been sequenced to get insight into the physiology of the two strains. Strain BC degrades benzene with chlorate as electron acceptor. The cyclohexanol-degrading denitrifying strain K601T is not able to use chlorate as electron acceptor, while strain BC cannot degrade cyclohexanol. The 16S rRNA sequences of strains BC and K601T are identical and the fatty acid methyl ester patterns of the strains are similar. Basic Local Alignment Search Tool (BLAST) analysis of predicted open reading frames of both strains showed most hits with Acidovorax sp. JS42, a bacterium that degrades nitro-aromatics. The genomes include strain-specific plasmids (pAlide201 in strain K601T and pAlide01 and pAlide02 in strain BC). Key genes of chlorate reduction in strain BC were located on a 120 kb megaplasmid (pAlide01), which was absent in strain K601T. Genes involved in cyclohexanol degradation were only found in strain K601T. Benzene and toluene are degraded via oxygenase-mediated pathways in both strains. Genes involved in the meta-cleavage pathway of catechol are present in the genomes of both strains. Strain BC also contains all genes of the ortho-cleavage pathway. The large number of mono- and dioxygenase genes in the genomes suggests that the two strains have a broader substrate range than known thus far.

  9. Chemical Control of Pennesetum Purpureum Laboratory Trials

    Directory of Open Access Journals (Sweden)

    B.N Tripathi

    1977-10-01

    Full Text Available Dichloral urea, diethyl chloracetamide, nitrourea, chloralhydrate, sodium trichloroacetate, sodium borate, ammonium thiocynate, sodium arsenite, arsenic oxide-sulphuric acid mixture, sodium chlorate, maleic hydrazide and the salts containing inorganic ions Cu/sup 2+/, Co/sup 2+/, MoO/sub 4//sup 2-/ and Zn/sup 2+/ were tested in experimental plots for their phytotoxic activity on a hybrid variety of Pennesetum purpureum. Sodium borate (2500 Kg/hectare, Sodium arsenite (250 Kg/hectare and sodium chlorate (1000 Kg/hectare through soil and ammonium thiocyanate (100 Kg/hectare through direct spray function as growth retardants. Arsenic oxide-sulphuric acid (100 : 300 Kg/hectare spray kills the existing leaves. Sodium chlorate (250 Kg/hectare spray exerts phytocidal action on young plants (3 weeks. Maleic hydrazide (50 Kg/hectare exerts permanent growth suppressant action on older plants (height >=1 m and kills the existing leaves of younger plants (height=<0.5 m. Copper sulphate (100 Kg/hectare induces partial drying of existing leaves and cobalt sulphate in the same dose induces yellowing of leaves extending the period of growth beyond the season of maximum growth of the control. Ammonium molybdate and Zinc acetate in the same dose do not exert any perceptible effect.

  10. Synthesis of semiconductor polymers by inductive plasma; Sintesis de polimeros semiconductores por plasmas inductivos

    Energy Technology Data Exchange (ETDEWEB)

    Fernandez, G.; Cruz, G.; Olayo, M.G. [ININ, 52045 Ocoyoacac, Estado de Mexico (Mexico); Morales, J. [UAM-I, 09340 Mexico D.F. (Mexico)

    2003-07-01

    When carrying out the synthesis of semiconductor polymers by plasma it is important to consider the electric arrangement of the discharge since this it influences in the distribution of the energy of the particles in the reactor. The main electric arrangements in those that are developed the brightness discharges of radio frequency are resistive, capacitive and inductive. In the Laboratory of Materials processing by plasma of the ININ its have been worked different synthesis of polymers with resistive arrangements with good results. In this work the results of the synthesis and characterization of poly aniline and chlorate polyethylene by inductive plasma are presented. (Author)

  11. Traitement du foisonnement filamenteux dû à Microthrix parvicella par ajout de sels métalliques

    OpenAIRE

    Durban, N.; Juzan, L.; Krier, J.; Héduit, A.; Gillot, S.

    2012-01-01

    / Les dysfonctionnements biologiques dus au développement de bactéries filamenteuses posent de nombreux problèmes d’exploitation aux stations d'épuration du type boues activées. Le filament le plus souvent mis en cause dans ce type de dysfonctionnement en France est Microthrix parvicella. La solution curative la plus utilisée actuellement est la chloration, traitement efficace mais non spécifique, qui impacte également la biologie des boues activées. Une solution émergente consiste à ut...

  12. Aquatic macro algae of a region under Almirante Alvaro Alberto nuclear power plant influence. I. Spatial seasonal evaluation; Macroalgas marinhas da regiao sob influencia da Central Nuclear Almirante Alvaro Alberto (CNAAA), Saco de Piraquara de Fora, Angra dos Reis, RJ, Brasil. I. Avaliacao espaco-temporal

    Energy Technology Data Exchange (ETDEWEB)

    Pedrini, A.G. [Instituto de Radioprotecao e Dosimetria (IRD), Rio de Janeiro, RJ (Brazil)]|[Universidade Santa Ursula, Rio de Janeiro, RJ (Brazil). Centro de Ciencias Biologicas; Cassano, V.; Coelho, L.G.; Labronici, G.J. [Universidade do Estado, Rio de Janeiro, RJ (Brazil). Inst. de Biologia

    1994-12-31

    Marine macro algae from the area which is under in fluence of the heated and chlorate liquid effluent to the CNAAA were observed (1981-1983) at 3 collection points: Pingo Dagua, Velho Beach, discharge point. A total of 121 taxa were found: 29 Chlorophyta, 26 Phaeophyta and 66 Rhodophyta. The spring season was the richest in taxa (78) while autumn was the poorest (85). Overall, the data suggest that the point A (Pingo Dagua) macro algae community (which is similar to the discharge point (0,80) is adequate for the control of the CNAAA effluent impact ad Piraquara de Fora. (author). 11 refs, 5 figs, 1 tab.

  13. Evaluation of the sensitivity of three sublethal cytotoxicity assays in human HepG2 cell line using water contaminants

    OpenAIRE

    Jondeau, Adeline; DAHBI, Laurence; Bani-Estivals, Marie-Helene; Chagnon, Marie-Christine

    2006-01-01

    The in vitro toxicological index IC50 (the millimolar concentration of compound which inhibits response assay by 50% compared to the solvent control) of 11 water contaminants (acrylamide, atrazine, B[a]P, BPA, 2,4-DAT, 17-alphaEE, H(2)O(2), 4-OP, sodium bromate, sodium chlorate, sodium nitrate) was evaluated on the human hepatoma (HepG2) cells using three short-term bioassays related to their morbidity status [radiometric RNA synthesis assay (RNA), luminometric ATP assay (ATP), fluorometric A...

  14. Ion exchange purification of scandium

    Science.gov (United States)

    Herchenroeder, Laurie A.; Burkholder, Harvey R.

    1990-10-23

    An improvement in purification of scandium through ion exchange chromatography is disclosed in which the oxidation potential of the eluting solution is altered by the addition of potassium chlorate or ammonium chloride so that removal of contaminants is encouraged. The temperature, pH and concentration of the eluent HEDTA are controlled in order to maintain the scandium in the column while minimizing dilution of the scandium band. Recovery of scandium is improved by pumping dilute scandium over the column prior to stripping the scandium and precipitation. This eliminates the HEDTA ion and other monovalent cations contaminating the scandium band. This method maximizes recovery of scandium while maintaining purity.

  15. The assessment of strain in materials using synchrotron radiation techniques and the role of strain in growth rate dispersion

    Science.gov (United States)

    Ristić, R. I.; Sherwood, J. N.; Wojciechowski, K.

    1994-11-01

    A question has been raised [Rule et al., J. Crystal Growth 123 (1992) 373] concerning the reliability of recent studies which we have made of the role of strain in defining growth rate dispersion in sodium chlorate microcrystals. A particular criticism was that our method of assessment of strain using synchrotron X-radiation was invalid due to the fact that radiation damage could have occurred in the samples. The authors also claimed that they could find no correlation between strain and growth rate. In this response we seek to define that the method of assessment of strain was sound.

  16. Evidence for the distribution of perchlorates on Mars

    Science.gov (United States)

    Clark, Benton C.; Kounaves, Samuel P.

    2016-10-01

    Various Mars missions have detected Cl atoms, chlorides and perchlorates in martian surface materials. The global soils, in particular, always contain significant levels of observable Cl. Direct evidence points to this Cl being in the form of both chlorides and perchlorates, and possibly also chlorates and other oxychlorines. The most widespread measurements have been of Cl atoms, and cannot discern the chemical form. However, from separate evidence of perchlorate obtained at high latitudes (Phoenix lander) and low latitudes (Curiosity rover), it is likely that perchlorates are widespread, albeit in varying proportions relative to the total amount of ubiquitous Cl.

  17. 危险货物介绍(30)%Introduction to Dangerous Goods (30)

    Institute of Scientific and Technical Information of China (English)

    莫道

    2001-01-01

    @@ 俗称:白药粉,白药,洋硝,盐酸加里 英文名称:Potassium Chlorate 分子式:KCLO3 特性:为透明无色结晶或白色粉末.味咸而凉,可与铵的化合物、易燃物或细碎金属粉末组成爆炸性混合物.与易燃物的混合物对摩擦敏感,与硫酸接触易着火或爆炸.

  18. 催化动力学法测定人发中痕量硒%CATALYTIC KINETIC SPECTROPHOTOMETRIC DETERMINATION OF TRACE SELENIUM(Ⅳ) IN HUMAN HAIR

    Institute of Scientific and Technical Information of China (English)

    仇佩虹; 林丽; 叶晓霞; 叶小琴

    2001-01-01

    A new catalytic kinetic method for determining trace selenium(Ⅳ) was described.Se(Ⅳ) can catalyze the discolouring of 2-(5-Bromo-2-Pyridylazo)-5-diethylaminophenol(5-Br-PADAP) by potassium chlorate in hydrochloric acid medium.The detection limit for Se(Ⅳ) is 5.7×10-5μg/ml.The linear range of determination is 0~0.4μg/25ml Se(Ⅳ).Satisfactory results may be obtained by direct determination of trace Se(Ⅳ) in human hair.

  19. Metabolism and pharmacokinetics of alternate drinking water disinfectants.

    OpenAIRE

    Abdel-Rahman, M S; Couri, D; Bull, R J

    1982-01-01

    The chlorination of surface waters is known to elevate trihalomethanes; consequently, chlorine dioxide (ClO2) is being considered as an alternative disinfectant. The primary products resulting from ClO2 disinfection of waters are chlorites (ClO2-) and chlorates (ClO3-). Studies in rats revealed that ClO2 is converted to chloride (Cl-), ClO2- and ClO3-. ClO2- and ClO3- are excreted as Cl-, ClO2- and Cl-, ClO2-, ClO3-, respectively. Radioactivity was rapidly absorbed from the gastrointestinal t...

  20. Contact Electrification of Regolith Particles and Chloride Electrolysis: Synthesis of Perchlorates on Mars

    Science.gov (United States)

    Tennakone, K.

    2016-10-01

    Contact electrification of chloride-impregnated martian regolith particles due to eolian agitation and moisture condensation on coalesced oppositely charged grains may lead to spontaneous electrolysis that generates hypochlorite, chlorite, chlorate, and perchlorate with a concomitant reduction of water to hydrogen. This process is not curtailed even if moisture condenses as ice because chloride ionizes on the surface of ice. Limitations dictated by potentials needed for electrolysis and breakdown electric fields enable estimation of the required regolith grain size. The estimated dimension turns out to be of the same order of magnitude as the expected median size of martian regolith, and a simple calculation yields the optimum rate of perchlorate production.

  1. Model Building of Disinfection-related By-product in Drinking Water Treatment%水消毒过程无机副产物生成模型的建立

    Institute of Scientific and Technical Information of China (English)

    胡本涛; 崔崇威

    2009-01-01

    探讨了饮用水ClO2消毒无机副产物ClO2和ClO3-产生预测模型建立的必要性.分析了模型建立的方法与过程,并提出存在的不足与建议.%The paper discusses necessity of building predicting model of chlorine and chlorate by - product in drinking water treatment. Methods and processes using for the modelare analyzed. And deficiencies and sugges-tions were brought forward.

  2. QUALITE DE L'EAU DE CONSOMMATION DANS LA COMMUNE DE SOUMAA (BLIDA - ALGERIE

    Directory of Open Access Journals (Sweden)

    F. HAMAIDI - CHERGUI

    2016-09-01

    Full Text Available Cette étude a été réalisée en vue d’apporter des rép onses convaincantes aux préoccupations des consommateurs de la commune de Soumaa sur la qualité de l'eau de robinet. Pour évaluer l’efficacité du traitement (chloration, un suivi saisonnier durant une période de sept mois de la qualité bactériologique des échantillons d'eau prélevés depuis la source (oued Bouchemla jusqu'au point d'usage, en passant par le stade d'eau traitée (après sa chloration a été effectué. Les résultats obtenus pour les 49 échantillons prélevés ont montré que : - 57,14% des échantillons d'eau prélevés après son traitement présentent un chlore positif, et 42,85% des échantillons sont de bonne qualité bactériologique. -60% des prélèvements effectués auprès des consommateurs sont de bonne qualité bactériologique, parmi eux, 34,28% ont présenté un chlore négatif.

  3. Chloroxyanion Residues in Cantaloupe and Tomatoes after Chlorine Dioxide Gas Sanitation.

    Science.gov (United States)

    Smith, D J; Ernst, W; Herges, G R

    2015-11-01

    Chlorine dioxide gas is effective at cleansing fruits and vegetables of bacterial pathogens and(or) rot organisms, but little data are available on chemical residues remaining subsequent to chlorine gas treatment. Therefore, studies were conducted to quantify chlorate and perchlorate residues after tomato and cantaloupe treatment with chlorine dioxide gas. Treatments delivered 50 mg of chlorine dioxide gas per kg of tomato (2-h treatment) and 100 mg of gas per kg of cantaloupe (6-h treatment) in sealed, darkened containers. Chlorate residues in tomato and cantaloupe edible flesh homogenates were less than the LC-MS/MS limit of quantitation (60 and 30 ng/g respectively), but were 1319 ± 247 ng/g in rind + edible flesh of cantaloupe. Perchlorate residues in all fractions of chlorine dioxide-treated tomatoes and cantaloupe were not different (P > 0.05) than perchlorate residues in similar fractions of untreated tomatoes and cantaloupe. Data from this study suggest that chlorine dioxide sanitation of edible vegetables and melons can be conducted without the formation of unwanted residues in edible fractions. PMID:26496046

  4. Depth profiling for the identification of unknown substances and concealed content at remote distances using time-resolved stand-off Raman spectroscopy.

    Science.gov (United States)

    Zachhuber, Bernhard; Gasser, Christoph; Ramer, Georg; Chrysostom, Engelene t H; Lendl, Bernhard

    2012-08-01

    Time-resolved stand-off Raman spectroscopy was used to determine both the position and identity of substances relative to each other at remote distances (up to tens of meters). Spectral information of three xylene isomers, toluene, and sodium chlorate was obtained at a distance of 12 m from the setup. Pairs and triplets of these samples were placed at varying distances (10-60 cm) relative to each other. Via the photon time of flight the distance between the individual samples was determined to an accuracy of 7% (corresponding to a few cm) of the physically measured distance. Furthermore, at a distance of 40 m, time-resolved Raman depth profiling was used to detect sodium chlorate in a white plastic container that was non-transparent to the human eye. The combination of the ranging capabilities of Raman LIDAR (sample location usually determined using prior knowledge of the analyte of interest) with stand-off Raman spectroscopy (analyte detection at remote distances) provides the capability for depth profile identification of unknown substances and analysis of concealed content in distant objects. To achieve these results, a 532 nm laser with a pulse length of 4.4 ns was synchronized to an intensified charge-coupled device camera with a minimum gate width of 500 ps. For automated data analysis a multivariate curve resolution algorithm was employed. PMID:22800681

  5. Analysis of P(VdCl-co-AN-co-MMA)-LiClO4-EC triblock copolymer electrolytes

    Indian Academy of Sciences (India)

    D Inbavalli; S Selvasekarapandian; C Sanjeeviraja; R Baskaran; S Nithya; Junichi Kawamura; Yoshitake Masuda

    2015-02-01

    The lithium ion conducting copolymer electrolytes based on poly(vinylidene chloride-co-acrylonitrileco- methyl methacrylate) P(VdCl-co-AN-co-MMA)-lithium per chlorate (LiClO4) (P(VdCl-co-AN-co-MMA): LiClO4) and poly(vinylidene chloride-co-acrylonitrile-co-methyl methacrylate)P(VdCl-co-AN-co-MMA)-lithium per chlorate (LiClO4)-ethylene carbonate (EC) (P(VdCl-co-AN-co-MMA):LiClO4:EC) of different compositions were prepared by solution-casting technique. Structural and surface morphological characterizations were studied by X-ray diffraction analysis and scanning electron microscopy measurements, respectively. Thermal and conductivity behaviour of copolymer–salt and copolymer–salt–plasticizer complexes were studied by employing differential scanning calorimetry and AC impedance measurements, respectively. The highest bulk conductivity was found to be 1.94 × 10-4 S cm-1 at 303 K for the plasticized sample. The dielectric behaviour and relaxation parameters of the samples have been presented and discussed.

  6. The influence of synchrotron radiation-induced strain on the growth and dissolution of brittle and ductile materials

    Science.gov (United States)

    Ristic, R. I.; Shekunov, B. Yu.; Sherwood, J. N.

    1997-08-01

    Sodium chlorate (brittle) and sodium nitrate (ductile) crystals were irradiated by synchrotron radiation to produce samples in which one-half of a particular crystal was strained by radiation damage and the other not. The growth and dissolution kinetics of these samples were investigated using in situ laser interferometry and X-ray topography. An appreciable difference was observed in the growth and dissolution kinetics of the irradiated and nonirradiated halves. In the region of very low supersaturation, σ < σ c = 0.32% for sodium chlorate and σ < σ c = 0.065% for sodium nitrate, the irradiated portions of both types of crystals dissolved; simultaneously, the nonirradiated portions grew. Above the critical supersaturation, σ c, both halves grew. This defines a difference in solubility between the irradiated and nonirradiated material. The significant difference between the two critical supersaturations in the two materials confirms our earlier findings that a larger amount of elastic strain per unit volume can be introduced into brittle materials than into ductile ones. This, in turn, has a much stronger effect on both growth and dissolution kinetics. Irradiation is shown to yield pure point defect strain and not to introduce dislocations in the system. A possible mechanism by which strain influences the growth and dissolution kinetics is discussed.

  7. 海砂对混凝土耐久性的影响及其淡化处理%Effect of sea sand on concrete durability and the desalination

    Institute of Scientific and Technical Information of China (English)

    贺烽; 韩继先

    2015-01-01

    近年来,随着河砂开采的限制和资源的匮乏,海砂在沿海地区建筑行业中的使用越来越普遍.介绍了我国的海砂资源情况和海砂性能特征,并分析了海砂中盐类尤其是氯盐和杂质对混凝土耐久性能的影响.海砂通过淡化处理,可以很好地去除其中有害的盐类和杂质,从而可确保淡化后的海砂在建筑工程中的安全可靠应用.%In recent years, with the restricted mining and resource-poor of river sand, the utilization of sea sand in construction indus?try of coastal area is more and more common. China sea sand resource and performance characteristics are introduced, and the effects of chlorate and impurities in sea sand on concrete durability are analysed. By desalinating the harmful chlorate and impurities in sea sand can be moved effectively, which guarantees safe and reliable application of desalted sea sand in construction engineering.

  8. Dissimilatory reduction of perchlorate and other common pollutants by a consortium enriched from tidal flats of the Yellow Sea

    Institute of Scientific and Technical Information of China (English)

    Nirmala Bardiya; Jae-Ho Bae

    2015-01-01

    Objective: To enrich a facultative anaerobic bacterial consortium from the Yellow Sea and assess its ability to reduce perchlorate and other co-pollutants. Methods: Bacterial consortium collected from the tidal flats of the Yellow Sea was enriched in an anoxic medium containing perchlorate as the electron (e-) acceptor and acetate as the electron (e-) donor. The enriched consortium was then tested for perchlorate reduction under different perchlorate concentrations and in the presence of nitrate by using standard anaerobic techniques. The complete enzymatic reduction of perchlorate to chloride was confirmed by chlorite dismutation. Ability of the consortium to grow with alternate e- acceptors was also tested with acetate as the e- donor. Results: The enriched consortium could rapidly reduce perchlorate up to the initial concentration of 25.65 mmol/L. In the presence of nitrate, perchlorate reduction did not occur immediately and reduction of nitrate started after a lag phase, with concomitant accumulation of nitrite. The perchlorate-enriched consortium could reduce chlorate, oxygen, Cr (VI), and selenate as the alternate e- acceptors but failed to utilize sulfate, thiosulfate, sulfite, and nitrite. Conclusions: The consortium from the tidal flats of the Yellow Sea could reduce perchlorate and co-contaminants such as chlorate, nitrate, Cr (VI), and selenate under heterotrophic conditions with acetate as the e- donor and carbon source. While perchlorate was completely dismutated into innocuous chloride and oxygen, accumulation of nitrite occurred during the reduction of nitrate.

  9. The measures to improve conversion rate of chlorine dioxide in methanol method process%提高甲醇法二氧化氯制备工艺转化率的措施

    Institute of Scientific and Technical Information of China (English)

    徐萃声; 詹磊; 黄丙贵

    2016-01-01

    在强酸性环境下,甲醇可以与氯酸钠发生氧化还原反应,氯酸钠由此被还原而产生二氧化氯,人们将这种二氧化氯制备方法称之为甲醇法。纸浆漂白甲醇法二氧化氯制备系统国产化已经实现,目前已成功运行多套系统。本文分析了影响纸浆漂白甲醇法二氧化氯系统工艺转化率的相关因素,并结合生产实际提出了相应的改进措施。%Methanol can make oxidation-reduction reaction with sodium chlorate under strong acid situation. Sodium chlorate is restored to make chlorine dioxide, which is called methanol method to prepare chlorine dioxide. The methanol method for chlorine dioxide preparation has been localized successfully, which has been well proven in many projects in bleaching plant in pulp industry. In this article were analyzed the relating factors of conversion rate of chlorine dioxide which is used in pulp bleaching process, and was put forward the corresponding improving measures combined with the production practice.

  10. Occurrence of persistent pollutants in soils, waters and firns of the Pirin mountains of Bulgaria; Persistente organische Schadstoffe in Boeden, Gewaessern und in Firn der Region noerdliche Piringebirge (Bulgarien)

    Energy Technology Data Exchange (ETDEWEB)

    Grunewald, K. [Technische Univ. Dresden (Germany). Inst. fuer Geographie; Schmidt, W. [DVGW - Technologiezentrum Wasser, Karlsruhe, TZW Aussenstelle Dresden (Germany)

    2001-07-01

    Systematic environmental screenings are still the exception in South-Eastern Europe. Especially, there is a decisive lack of information concerning the occurrence and behaviour of xenobiotic and toxic compounds like volatile- and non volatile halogenated organics, suppressed by the surrogate AOX, synthetic chelating agents, pesticides, like DDT as well as chlorate in the biosphere. The analysis of soils, waters, and firns of a representative area in Bulgaria, the Pirin mountains, indicate a relatively low back ground pollution. The accumulation of the xenobiotics in this high mountain region is recognised to be low. Nevertheless, traces of pesticides and chelating agents like EDTA and NTA in ice (firns) and soils were found. The surrogate AOX should be a parameter, suitable for routine environmental screenings of such areas. (orig.) [German] Systematische Umweltuntersuchungen stellen in Suedosteuropa noch eine Ausnahme dar. Dies betrifft insbesondere die Analyse organischer Schadstoffe, die innerhalb der Biosphaere zu toxischen Wirkungen fuehren koennen. In einer repraesentativen Region in Suedwest-Bulgarien wurden Boden-, Firn- und Wasserproben auf AOX, CKW, Chlorat, synthetische Komplexbildner, Insektizide und Herbizide untersucht. Die Hintergrundbelastung der analysierten Stoffe in Boeden und Waessern ist relativ niedrig. Eine vermutete Akkumulation persistenter organischer Chemikalien im Hochgebirge Pirin wurde nur teilweise bestaetigt. Nachgewiesen wurden Insektizidrueckstaende und die synthetischen Komplexbildner EDTA und NTA in Firnproben sowie AOX in Substratmaterial. AOX bietet sich als Parameter zur Umweltueberwachung in der Region an. Die Analyse weiterer POPs steht noch an. (orig.)

  11. Unusual inherent electrochemistry of graphene oxides prepared using permanganate oxidants.

    Science.gov (United States)

    Eng, Alex Yong Sheng; Ambrosi, Adriano; Chua, Chun Kiang; Saněk, Filip; Sofer, Zdeněk; Pumera, Martin

    2013-09-16

    Graphene and graphene oxides are materials of significant interest in electrochemical devices such as supercapacitors, batteries, fuel cells, and sensors. Graphene oxides and reduced graphenes are typically prepared by oxidizing graphite in strong mineral acid mixtures with chlorate (Staudenmaier, Hofmann) or permanganate (Hummers, Tour) oxidants. Herein, we reveal that graphene oxides pose inherent electrochemistry, that is, they can be oxidized or reduced at relatively mild potentials (within the range ±1 V) that are lower than typical battery potentials. This inherent electrochemistry of graphene differs dramatically from that of the used oxidants. Graphene oxides prepared using chlorate exhibit chemically irreversible reductions, whereas graphene oxides prepared through permanganate-based methods exhibit very unusual inherent chemically reversible electrochemistry of oxygen-containing groups. Insight into the electrochemical behaviour was obtained through cyclic voltammetry, chronoamperometry, and X-ray photoelectron spectroscopy experiments. Our findings are of extreme importance for the electrochemistry community as they reveal that electrode materials undergo cyclic changes in charge/discharge cycles, which has strong implications for energy-storage and sensing devices.

  12. Functional complementation of a nitrate reductase defective mutant of a green alga Dunaliella viridis by introducing the nitrate reductase gene.

    Science.gov (United States)

    Sun, Yu; Gao, Xiaoshu; Li, Qiyun; Zhang, Qingqi; Xu, Zhengkai

    2006-08-01

    Nitrate reductase (NR) catalyzes NAD (P) H dependent reduction of nitrate to nitrite. Transformation systems have been established in several species of green algae by nitrate reductase gene functional complementation. In this report, an endogenous NR cDNA (3.4 kb) and a genomic fragment (14.6 kb) containing the NR gene (DvNIA1) were isolated from the D. viridis cDNA and genomic libraries respectively. Southern blot and Northern blot analyses showed that this gene exists as a single copy in D. viridis and is induced by nitrate. To obtain a NR defective mutant as a recipient strain, D. viridis cells were treated with a chemical mutagen and then cultured on a chlorate-containing plate to enrich chlorate tolerant mutants. Southern analysis showed that one isolate, B14, had a deletion in the DvNIA1 gene region. Using electroporation conditions determined in this laboratory, plasmid pDVNR containing the intact DvNIA1 gene has been electroporated into the defective mutant B14. Strains retaining a nitrate assimilation phenotype were obtained from nitrate plates after spreading the electroporated cells. In some individual strains, transcription of the introduced gene was detected. NR activity in these strains was slightly higher than that in the defective B14 cell, but excretion of nitrite into culture media was almost as high as that of the wild-type cell. Possible episomal presence of the introduced DNA in D. viridis is discussed. PMID:16797881

  13. The Investigation of Magnesium Perchlorate/Iron Phase-mineral Mixtures as a Possible Source of Oxygen and Chlorine Detected by the Sample Analysis at Mars (SAM) Instrument in Gale Crater, Mars

    Science.gov (United States)

    Sutter, B.; Heil, E.; Archer, P. D.; Ming, D. W.; Eigenbrode, J. L.; Franz, H. B.; Glavin, D. P.; McAdam, A. C.; Mahaffy, P. R.; Niles, P. B.; Stern, J. C.; Navarro-Gonzalez, R.; McKay, C. P.

    2014-01-01

    The Sample Analysis at Mars (SAM) instrument onboard the Curiosity rover detect-ed O2 and HCl gas releases from the Rocknest (RN) eolian bedform and the John Klein (JK) and Cumber-land (CB) drill hole materials in Gale Crater (Fig. 1) [1,2]. Chlorinated hydrocarbons have also been detect-ed by the SAM quadrupole mass spectrometer (QMS) and gas chromatography/mass spectrometer (GCMS) [1,2,3,4]. These detections along with the detection of perchlorate (ClO4(-)) by the Mars Phoenix Lander's Wet Chemistry Laboratory (WCL) [5] suggesting perchlo-rate is a possible candidate for evolved O2 and chlorine species. Laboratory thermal analysis of individual per-chlorates has yet to provide an unequivocal tempera-ture match to the SAM O2 and HCl release data [1,2]. Catalytic reactions of Fe phases in the Gale Crater ma-terial with perchlorates can potentially reduce the de-composition temperatures of these otherwise pure per-chlorate/chlorate phases [e.g., 6,7]. Iron mineralogy found in the Rocknest materials when mixed with Ca-perchlorate was found to cause O2 release temperatures to be closer match to the SAM O2 release data and enhance HCl gas releases. Exact matches to the SAM data has unfortnunately not been achieved with Ca-perchlorate-Fe-phase mixtures [8]. The effects of Fe-phases on magnesium perchlorate thermal decomposi-tion release of O2 and HCl have not been evaluated and may provide improved matches to the SAM O2 and HCl release data. This work will evaluate the thermal decomposition of magnesium perchlorate mixed with fayalite/magnetite phase and a Mauna Kea palagonite (HWMK 919). The objectives are to 1) summarize O2 and HCl releases from the Gale Crater materials, and 2) evaluate the O2 and HCl releases from the Mg-perchlorate + Fe phase mixtures to determine if Mg-perchlorate mixed with Fe-phases can explain the Gale Crater O2 and HCl releases.

  14. Enhanced chlorine dioxide decay in the presence of metal oxides: Relevance to drinking water distribution systems

    KAUST Repository

    Liu, Chao

    2013-07-19

    Chlorine dioxide (ClO2) decay in the presence of typical metal oxides occurring in distribution systems was investigated. Metal oxides generally enhanced ClO2 decay in a second-order process via three pathways: (1) catalytic disproportionation with equimolar formation of chlorite and chlorate, (2) reaction to chlorite and oxygen, and (3) oxidation of a metal in a reduced form (e.g., cuprous oxide) to a higher oxidation state. Cupric oxide (CuO) and nickel oxide (NiO) showed significantly stronger abilities than goethite (α-FeOOH) to catalyze the ClO2 disproportionation (pathway 1), which predominated at higher initial ClO2 concentrations (56-81 μM). At lower initial ClO2 concentrations (13-31 μM), pathway 2 also contributed. The CuO-enhanced ClO2 decay is a base-assisted reaction with a third-order rate constant of 1.5 × 10 6 M-2 s-1 in the presence of 0.1 g L -1 CuO at 21 ± 1 C, which is 4-5 orders of magnitude higher than in the absence of CuO. The presence of natural organic matter (NOM) significantly enhanced the formation of chlorite and decreased the ClO 2 disproportionation in the CuO-ClO2 system, probably because of a higher reactivity of CuO-activated ClO2 with NOM. Furthermore, a kinetic model was developed to simulate CuO-enhanced ClO 2 decay at various pH values. Model simulations that agree well with the experimental data include a pre-equilibrium step with the rapid formation of a complex, namely, CuO-activated Cl2O4. The reaction of this complex with OH- is the rate-limiting and pH-dependent step for the overall reaction, producing chlorite and an intermediate that further forms chlorate and oxygen in parallel. These novel findings suggest that the possible ClO2 loss and the formation of chlorite/chlorate should be carefully considered in drinking water distribution systems containing copper pipes. © 2013 American Chemical Society.

  15. Synthesis of polymer electrolyte membranes from cellulose acetate/poly(ethylene oxide)/LiClO4 for lithium ion battery application

    International Nuclear Information System (INIS)

    This study was conducted to determine the effect of cellulose acetate on poly(ethylene oxide)-LiClO4 membranes as the polymer electrolyte. Cellulose acetate is used as an additive to increase ionic conductivity and mechanical property of polymer electrolyte membranes. The increase the percentage of cellulose acetate in membranes do not directly effect on the ionic conductivity, and the highest ionic conductivity of membranes about 5,7 × 10−4 S/cm was observed in SA/PEO/LiClO4 membrane with cellulose ratio of 10-25% (w/w). Cellulose acetate in membranes increases mechanical strength of polymer electrolyte membranes. Based on TGA analysis, this polymer electrolyte thermally is stable until 270 °C. The polymer electrolyte membrane prepared by blending the cellulose acetate, poly(ethylene oxide), and lithium chlorate could be potentially used as a polymer electrolyte for lithium ion battery application

  16. The XPS study of physical and chemical forms of neptunium group on the surface of minerals

    Directory of Open Access Journals (Sweden)

    Teterin Anton Yu.

    2010-01-01

    Full Text Available The sorption behavior and the physical and chemical forms of neptunium on the surface of minerals of the two chlorate samples, biotite and kaolin, with different contents of Fe(II was studied. The liquid-liquid extraction and the X-ray photoelectron spectroscopy were employed to identify the valence forms of neptunium. On the basis of the obtained data the quantitative elemental composition of the surface of the studied minerals, as well as the ionic composition of the formed neptunium complexes was determined. It was shown that the Np(IV and Np(VI containing compounds did not form, while the complexes Np(VO+ -hydroxyl did form on the surface. The oxygen ions bonded with iron and oxygen belonging to water and/or of carboxyl were suggested to be present in the equatorial plane of the neptunyl group NpO+.

  17. Enhancement of gamma-ray-induced mutation frequency in rice by post-treatment with chloral hydrate, methanol and their mixtures with ethanol

    International Nuclear Information System (INIS)

    An evaluation has been made of the mutagenic activity of ethanol, chlorate hydrate (CH) and methanol on rice seed. In independent treatments with ethanol, methanol, CH and four aqueous mixtures of these chemicals, chlorophyll-deficient mutants were not recovered in the M2 generation. However, in sequential treatments with gamma rays + CH, gamma rays + methanol and gamma rays + aqueous mixtures of these chemicals, significant increases in the yields of chlorophyll mutations were observed as compared to that of a 30 kR gamma ray treatment. In contrast, post-irradiation treatment with ethanol failed to provoke any increase in the frequency of chlorophyll mutants in the M2 generation. The results indicate that CH and methanol alone and mixed with ethanol can potentiate gamma ray-induced genetic lesions in rice seed. (author)

  18. Biochemical and genetical characterization of nitrate reductase deficient mutants of Petunia.

    Science.gov (United States)

    Steffen, A; Schieder, O

    1984-08-01

    Four NR(-) lines were selected by their resistance to 100 mM chlorate from X-ray irradiated protoplasts of haploid Petunia hybrida var. Mitchell. The four cell lines were characterized by the presence of xanthine dehydrogenase activity and by complementation tests via protoplast fusion. One mutant (line 1) was classified as defective in the NR apoprotein (tentatively, nia-type) and the other three (lines 2, 3, 4) in the molybdenum cofactor (tentatively, cnx-type). Some NR activity (15 %) could be restored by adding unphysiologically high concentrations of molybdate to the culture medium in two of the cnx-lines (lines 3 and 4). The third cnx-line (line 2) had no NR activity. A complementation analysis via protoplast fusion confirmed that the mutants comprised 3 non-allelic groups. From these results it can be concluded that these NR(-) mutants are recessive and that two of the cnx-mutants (lines 3, 4) are allelic.

  19. CHLORINE DIOXIDE BLEACHING OF SODA-ANTHRAQUINONE JUTE PULP TO A VERY HIGH BRIGHTNESS

    Directory of Open Access Journals (Sweden)

    M. Sarwar Jahan

    2010-05-01

    Full Text Available Bleaching of soda-anthraquinone jute pulp by chlorine dioxide (ClO2 was studied to reach a target brightness of above 88% for the purpose of using less bleaching chemicals. The performance of either chlorine dioxide or peroxide in the final bleaching to boost brightness was also studied. The experimental results revealed that the final brightness depended on ClO2 charge in the Do and D1 stages. The brightness reversion was lower when the final stage brightening was done by peroxide. The use of Mg(OH2 in the D1 and D2 stages improved the final brightness due to the formation of less chlorate and chlorite during the Mg(OH2- based ClO2 brightening stages. The strength properties of pulp bleached by peroxide in the final stage was slightly better than that from ClO2 as the final ClO2 bleaching stage.

  20. Structural and electrochemical properties of PEMA with the influence of MWCNT / TiO2 filler

    Science.gov (United States)

    Pradeepa, P.; Raj, S. Edwin; Kalaiselvimary, J.; Sowmya, G.; Selvakumar, K.; Prabhu, M. Ramesh

    2016-05-01

    An attempt has been made to prepare a hybrid Nano composite polymer electrolytes (NCPES) based on Poly(ethyl methacrylate) (PEMA) doped with multiwalled carbon nanotubes (MWCNT) and Titanium oxide (TiO2) as additives, Lithium per chlorate (LiClO4) as ionic salt and Propylene Carbonate as plasticizer (PC) by using solvent casting technique. X-ray diffraction analysis (XRD) confirms the miscibility and amorphous nature of the prepared electrolytes. It has been found from the a.c impedance analysis that the inorganic filler reduces the bulk resistance of the electrolytes and thus ionic conductivity enhanced. A high dielectric loss value is observed for the case of doped MWCNT-PEMA in comparison with pure PEMA and doped TiO2 -PEMA membranes. Based on the study of relaxation spectra, it is found that the relaxation time decreases with increase in temperature.

  1. Synthesis of polymer electrolyte membranes from cellulose acetate/poly(ethylene oxide)/LiClO{sub 4} for lithium ion battery application

    Energy Technology Data Exchange (ETDEWEB)

    Nurhadini,, E-mail: nur-chem@yahoo.co.id; Arcana, I Made, E-mail: arcana@chem.itb.ac.id [Inorganic and Physical Chemistry Research Division, Faculty of Mathematics and Natural Sciences, Institiut Teknologi Bandung, Jalan Ganesha 10, Bandung 40132 (Indonesia)

    2015-09-30

    This study was conducted to determine the effect of cellulose acetate on poly(ethylene oxide)-LiClO{sub 4} membranes as the polymer electrolyte. Cellulose acetate is used as an additive to increase ionic conductivity and mechanical property of polymer electrolyte membranes. The increase the percentage of cellulose acetate in membranes do not directly effect on the ionic conductivity, and the highest ionic conductivity of membranes about 5,7 × 10{sup −4} S/cm was observed in SA/PEO/LiClO{sub 4} membrane with cellulose ratio of 10-25% (w/w). Cellulose acetate in membranes increases mechanical strength of polymer electrolyte membranes. Based on TGA analysis, this polymer electrolyte thermally is stable until 270 °C. The polymer electrolyte membrane prepared by blending the cellulose acetate, poly(ethylene oxide), and lithium chlorate could be potentially used as a polymer electrolyte for lithium ion battery application.

  2. Synthesis of polymer electrolyte membranes from cellulose acetate/poly(ethylene oxide)/LiClO4 for lithium ion battery application

    Science.gov (United States)

    Nurhadini, Arcana, I. Made

    2015-09-01

    This study was conducted to determine the effect of cellulose acetate on poly(ethylene oxide)-LiClO4 membranes as the polymer electrolyte. Cellulose acetate is used as an additive to increase ionic conductivity and mechanical property of polymer electrolyte membranes. The increase the percentage of cellulose acetate in membranes do not directly effect on the ionic conductivity, and the highest ionic conductivity of membranes about 5,7 × 10-4 S/cm was observed in SA/PEO/LiClO4 membrane with cellulose ratio of 10-25% (w/w). Cellulose acetate in membranes increases mechanical strength of polymer electrolyte membranes. Based on TGA analysis, this polymer electrolyte thermally is stable until 270 °C. The polymer electrolyte membrane prepared by blending the cellulose acetate, poly(ethylene oxide), and lithium chlorate could be potentially used as a polymer electrolyte for lithium ion battery application.

  3. Synthesis by plasma and characterization of semiconductor compounds derived of polyacetylene; Sintesis por plasma y caracterizacion de compuestos semiconductores derivados del poliacetileno

    Energy Technology Data Exchange (ETDEWEB)

    Vasquez, M.; Cruz, G. [ININ, 52045 Ocoyoacac, Estado de Mexico (Mexico); Timoshina, T. [ESIQIE-IPN, 07738 Mexico D.F. (Mexico); Olayo, R. [UAM-I, 09340 Mexico D.F. (Mexico)

    2003-07-01

    In this work it is made a study of the structure and electric properties of chlorate polyethylene (PE-CI) with double and simple bonds obtained by continuous plasma with resistive coupling to 13.5 MHz. The synthesis conditions are power between 10 and 14 W and pressure of (6-7) x 10{sup -2} Torr. The synthesized PE-Cl in that way is soluble in acetone what indicates that probably is formed of short chains and not it shows the generalized inter crossing that is presented in some syntheses by plasma and that it can degrade the electric properties of these polymers. The IR and XPS analysis show the vibration of the C-C, C=C and C-CI bonds. The morphology of the polymer after being dissolved shows a compact and flat configuration. The electric conductivity has an approximately lineal behavior in an interval of 35 to 90% of relative humidity. (Author)

  4. Mass transfer in the absorption of SO2 and NOx using aqueous euchlorine scrubbing solution

    Institute of Scientific and Technical Information of China (English)

    DESHWAL Bal-Raj; LEE Hyung-Keun

    2009-01-01

    Attempts have been made to generate euchlorine gas by chlorate-chloride process and to utilize it further to clean up SO2 and NOx from the flue gas in a lab scale bubbling reactor.Preliminary experiments were carried out to determine the gas and liquid phase mass transfer coefficients and their correlation equations have been established.Simultaneous removal of SO2 and NOx from the simulated flue gas using aqueous euchlorine scrubbing solution has been investigated.Euchlorine oxidized NO into NO2 completely and the later subsequently absorbed into the scrubbing solution in the form of nitrate.SO2 removal efficiency of around 100% and NOx removal efficiency of around 72 % were achieved under optimized conditions.Mass balance has been confirmed by analyzing the sulfate, nitrate, euchlorine and chloride ion using ion chromatograph/auto-titrator and comparing it with their corresponding calculated values.

  5. Determination of ribavirin by flow injection chemiluminescence

    Institute of Scientific and Technical Information of China (English)

    Juqing Jin; Yuhai Tang; Langchong He; Hong Yao; Yuanyuan Sun

    2006-01-01

    Objective: To establish a rapid and precise continuous flow-injection chemiluminescence (CL) method to determine ribavirin. Methods: The ribavirin could restrain strongly CL reaction of luminol in sodium hydroxide (NaOH) solution with potassium chlorate(KClO3). The different experimental parameters affecting the CL intensity were studied carefully. Results:Under optimum conditions(The concentrations of luminol,KClO3, and NaOH were at 0.1 mmol/L,0.5 μmol/L,and 0.2 mol/L, respectively), the linear range of the working curves was 0.01-7.00 μg/ml with a detection limit of 0.004 μg/ml. Conclusion: The method is simple, rapid and sensitive, and successfully applied to the determination of ribavirin in pharmaceutical preparations and biological fluids.

  6. Preparation and characterization of CoFe2O4/TiO2 magnetic composite films

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    CoFe2O4/TiO2 magnetic composite films were prepared using the sol-gel method with tetrabutyltitanate and metallic chlorates as starting materials. The effects of heat treatment temperatures on micro- structures and on magnetic properties were studied. The microstructure and properties of the samples at different heat treatment temperatures were characterized by X-ray diffraction, Raman spectrum, scanning electron microscopy, polarized microscopy and vibrating sample magnetometry. The results show that crystals of different substances grow up independently. Cobalt ferrite is evenly embedded into the titanium dioxide matrix in the prepared composite films. The magnetism of the composite films is enhanced with an increase of the heat temperature.

  7. Optøjer og dioxiner

    DEFF Research Database (Denmark)

    Berg, Rolf W.

    2008-01-01

    Forhåbentlig er vinterens dille med afbrændte biler et overstået fænomen. En bilbrand kan nemlig udlede store mængder dioxin - et of de giftigste molekyler, vi kender. Optøjerne kan derfor være en anledning tit at slå fast, at det i det hele taget er en dårlig ide at brænde materialer af, der kan...... bandlyst, ligesom fyrværkeri (sædvanligvis baseret på chlorater) næppe er godt i forhold til dioxin-udsendelse. I brændeovne bør man under ingen omstændigheder afbrænde PVC og andet chlor-holdigt affald. Faktaboks med detaljer om dioxin....

  8. 新型消毒剂-ClO2的制备方法及应用现状%PREPARATION OF NEW DISINFECTANT-ClO2 AND ITS APPLICATION

    Institute of Scientific and Technical Information of China (English)

    郑建华; 韩舞鹰

    2001-01-01

    The preparation method of ClO2, its some present products and application are introduced in this paper. Its preparation methods mainly include chemical and electrolysis methods, and their raw materials are mainly sodium chlorate, sodium chlorite and table salt. The present chloride dioxide products are mainly the stable ClO2 aqueous solution and solid chloride dioxide; the solid chloride dioxide has adsorbing type, gelatifying type and mono-packing type etc. due to different preparation technique. They are extensively applied to the aspects of disinfection, sterilization, algue removal, pulp-bleaching, air purification, food antisepsis and retaining freshness etc. of drinking water, industrial wastewater, hospital sewage, industrial cycle cooling water, fowl slaughter, indoor hygiene, beer production and aquiculture etc.%本文详细地介绍了二氧化氯的制备方法和现有的几种二氧化氯制品及其应用。

  9. Reversed flow injection spectrophotometric determination of low residuals of chlorine dioxide in water using chlorophenol red

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    A novel,simple,rapid,sensitive and highly selective flow injection procedure for the spectrophotometrie determination of chlorine dioxide in the presence of other chlorine species,viz,free chlorine,chlorite,chlorate and hypoehlorite,is developed.The method is based on the discoloration reaction between chlorine dioxide and chlorophenol red and can overcome the shortcomings existed in direct speetrophotometrie determination for chlorine dioxide owing to the serious interference of free and combined chlorine.The procedure gave a linear calibration graph over the range 0-0.71 mg/L of chlorine dioxide.With a detection limit of 0.024 mg/L and a sample throughput of 60 samples/h.

  10. An industrial customer's view of changes in electricity purchasing

    International Nuclear Information System (INIS)

    The purchasing agent for Canadian Occidental Chemicals described his experiences in the purchase of electricity under the new circumstances of competition. Electrical power costs for Canadian Occidental's manufacturing operation were described as a key consideration in expanding their chlorate production. The ideal purchasing scheme was described from the purchaser's standpoint. A list of what purchasers wish to gain from increased supplier choices was provided. The behaviour of the electricity suppliers that provide power to CanadianOccidental was described since changes in British Columbia's electric power regulations were enacted. Electric utility marketing practices in Ontario, Manitoba and Alberta were noted in comparison. It was prophesized that deeregulation will ultimately benefit consumers and provincial economies, by transforming the power industry into a customer driven industry

  11. Some Observations on the Ignition of Composite Solid Propellants

    Directory of Open Access Journals (Sweden)

    K. Kishore

    1995-07-01

    Full Text Available Heat-up times derived from studies on the ignition characteristics of a few model composite solid propellants, containing polystyrene, carboxy-terminated polybutadiene, plasticised polyvinyl chloride and polyphenol formaldehyde as binders, show that they are directly proportional to the mass of the sample and inversely proportional to the heat flux. Propellant weight-loss prior to ignition and high pressure ignition temperature data on the propellants, ammonium per chlorate, and binders show that the ignition is governed by the gasification of the binder pyrolysis products. The activation energy for the gasification of the pyrolysed polymer products corresponds to their ignition behaviour suggesting that propellant ignition is controlled by the binder.

  12. Multidimensional detection of explosives and explosive signatures via laser electrospray mass spectrometry

    Science.gov (United States)

    Brady, John J.; Flanigan, Paul M., IV; Perez, Johnny J.; Judge, Elizabeth J.; Levis, Robert J.

    2012-06-01

    Nitro- and inorganic-based energetic material is vaporized at atmospheric pressure using nonresonant, 70 femtosecond laser pulses prior to electrospray post-ionization and transfer into a time-of-flight mass spectrometer for mass analysis. Measurements of a nitro-based energetic molecule, cyclotrimethylenetrinitramine (RDX), adsorbed on metal and dielectric surfaces indicate nonresonant vaporization of intact molecules, demonstrating the universality of laser electrospray mass spectrometry (LEMS) technique for explosives. In addition, RDX is analyzed at a distance of 2 meters to demonstrate the remote detection capability of LEMS. Finally, the analysis and multivariate statistical classification of inorganic-based explosives containing ammonium nitrate, chlorate, perchlorate, black powder, and an organic-based explosive is presented, further expanding the capabilities of the LEMS technique for detection of energetic materials.

  13. Survey of electrochemical production of inorganic compounds. Final report

    Energy Technology Data Exchange (ETDEWEB)

    1980-10-01

    The electrochemical generation of inorganic compounds, excluding chlorine/caustic, has been critically reviewed. About 60 x 10/sup 12/ Btu/y fossil fuel equivalent will be used in the year 2000 for the electrosynthesis of inorganic compounds. Significant energy savings in chlorate production can result from the development of suitable electrocatalysts for lowering the cathodic overpotential. Perchlorates, electrolytic hypochlorite, electrolytic manganese dioxide, fluorine and other miscellaneous compounds use relatively small amounts of electrical energy. Implementation of caustic scrubber technology for stack gas cleanup would result in appreciable amounts of sodium sulfate which could be electrolyzed to regenerate caustic. Hydrogen peroxide, now produced by the alkyl anthraquinone process, could be made electrolytically by a new process coupling anodic oxidation of sulfate with cathodic reduction of oxygen in alkaline solution. Ozone is currently manufactured using energy-inefficient silent discharge equipment. A novel energy-efficient approach which uses an oxygen-enhanced anodic reaction is examined.

  14. Detection of DNA Hypomethylation Mediated Floral Induction in Longan and Spinach Using the HAT-RAPD Technique

    Directory of Open Access Journals (Sweden)

    S. Anuntalabhochai

    2009-01-01

    Full Text Available In this study, the HAT-RAPD technique was used to detect DNA methylation in the four plant species, rice (Oryza sativa, petunia (Petunia hybrida, spinach (Spinacea oleracea L. and longan (Dimocarpus longan Lour., which were treated using 5-azacytidine, potassium chlorate (KClO3 and a low temperature induction. Rice and petunia were chosen to be induced because in these species it is known that 5-azacytidine is able to induce hypomethylation in their genomes leading to morphological changes, in particular floral induction, in the developing plants. Using the HAT-RAPD technique, DNA methylation was detected using the restriction enzymes HpaII and MspI in rice and petunia (as expected and in spinach, but was found to be absent in longan, which suggests that floral induction in longan is undetectable in longan.

  15. Ion chromatography in the manufacture of multilayer circuit boards

    Science.gov (United States)

    Smith, Robert E.

    1990-09-01

    Ion chromatography (IC) has proven useful in analyzing chemical solutions used in the manufacture of multilayer circuit boards. The manufacturing process is described briefly and previously published IC methods are reviewed. Then, methods are described for determining chlorate and chlorite in a brown oxide solution; salicylic acid in an epoxy cure agent; formate, sulfate, and tartrate in an electroless copper bath; anionic detergents in a tin-lead brightener and in a cleaning solution; and aqueous photoresist and nonionic brightener in a tin-lead bath. Anion exchange, reverse phase HPLC on a poly(styrene/divinylbenzene), PS/DVB, column and 2-D liquid chromatography also are described. Chemically suppressed conductivity and photometric detection are used.

  16. Analysis of oxyhalide disinfection by-products and other anions of interest in drinking water by ion chromatography.

    Science.gov (United States)

    Hautman, D P; Bolyard, M

    1992-06-01

    The US Environmental Protection Agency is developing regulations for various drinking water disinfection by-products (DBPs). This effort involves developing analytical methods for the DBPs formed as a result of different disinfection treatments and collecting occurrence data for these species. Ion chromatography is one method being used to analyze drinking water samples for the following inorganic DBPs: chlorite, chlorate and bromate. These anions, however, are difficult to separate from common interfering anions of chloride, carbonate and nitrate. A method is therefore presented by which tetraborate/boric acid is used to separate these anions. Method detection limits of the order of 10 micrograms/l, using conductivity and UV detection were obtained. Stability studies of chlorite showing the effectiveness of ethylenediamine as a preservative and summary data for an occurrence of nitrite, nitrate and the DBP precursor bromide are presented.

  17. Alternative Electrode Materials and Ceramic Filter Minimize Disinfection Byproducts in Point-of-Use Electrochemical Water Treatment

    Science.gov (United States)

    Yoon, Yeojoon; Jung, Youmi; Kwon, Minhwan; Cho, Eunha; Kang, Joon-Wun

    2013-01-01

    Abstract Effects of various electrodes and prefiltration to minimize disinfection byproducts (DBPs) in electrochemical water disinfection was evaluated. The target microorganism, Escherichia coli O157:H7, was effectively inactivated even applying a solar-charged storage battery for the electrolysis process. Extent of microbial inactivation decreased with lower water temperature and higher pH in the free chlorine disinfection system. The RuO2/Ti electrode was most efficient because it produced the lowest concentration of chlorate and the highest generation of free chlorine. Prefiltration using a ceramic filter inhibited formation of halogenated DBPs because it removed precursors of DBPs. For safe point-of-use water treatment, the use of a hybrid prefiltration stage with the electrolysis system is strongly recommended to reduce risks from DBPs. The system is particularly suited to use in developing regions. PMID:24381482

  18. Alternative Electrode Materials and Ceramic Filter Minimize Disinfection Byproducts in Point-of-Use Electrochemical Water Treatment.

    Science.gov (United States)

    Yoon, Yeojoon; Jung, Youmi; Kwon, Minhwan; Cho, Eunha; Kang, Joon-Wun

    2013-12-01

    Effects of various electrodes and prefiltration to minimize disinfection byproducts (DBPs) in electrochemical water disinfection was evaluated. The target microorganism, Escherichia coli O157:H7, was effectively inactivated even applying a solar-charged storage battery for the electrolysis process. Extent of microbial inactivation decreased with lower water temperature and higher pH in the free chlorine disinfection system. The RuO2/Ti electrode was most efficient because it produced the lowest concentration of chlorate and the highest generation of free chlorine. Prefiltration using a ceramic filter inhibited formation of halogenated DBPs because it removed precursors of DBPs. For safe point-of-use water treatment, the use of a hybrid prefiltration stage with the electrolysis system is strongly recommended to reduce risks from DBPs. The system is particularly suited to use in developing regions.

  19. Drinking Water Disinfection by In-line Electrolysis: Product and Inorganic By-Product Formation

    Science.gov (United States)

    Bergmann, M. E. Henry

    This section covers peculiarities of so-called in-line electrolysis when drinking water is electrolysed to produce disinfection species killing microorganisms. Mainly mixed oxide electrodes (MIO) based on IrO2 and/or RuO2 coatings and boron-doped diamond electrodes were used in the studies. Artificial and real drinking water systems were electrolysed in continuous and discontinuous operating mode, varying water composition, current density and electrode materials. Results show, besides the ability of producing active chlorine, risks of inorganic disinfection by-products (DBPs) such as chlorate, perchlorate, nitrite, ammonium, chloramines, hydrogen peroxide and others. DBPs are responsible for analysis errors using DPD method for active chlorine measurements. Geometry may influence by-product yield. As a conclusion, the necessity of developing test routines for practical cell applications must be underlined.

  20. Synthesis of Graphene Oxide by Oxidation of Graphite with Ferrate(VI) Compounds: Myth or Reality?

    Science.gov (United States)

    Sofer, Zdeněk; Luxa, Jan; Jankovský, Ondřej; Sedmidubský, David; Bystroň, Tomáš; Pumera, Martin

    2016-09-19

    It is well established that graphene oxide can be prepared by the oxidation of graphite using permanganate or chlorate in an acidic environment. Recently, however, the synthesis of graphene oxide using potassium ferrate(VI) ions has been reported. Herein, we critically replicate and evaluate this new ferrate(VI) oxidation method. In addition, we test the use of potassium ferrate(VI) for the synthesis of graphene oxide under various experimental routes. The synthesized materials are analyzed by a number of analytical methods in order to confirm or disprove the possibility of synthesizing graphene oxide by the ferrate(VI) oxidation route. Our results confirm the unsuitability of using ferrate(VI) for the oxidation of graphite on graphene oxide because of its high instability in an acidic environment and low oxidation power in neutral and alkaline environments.

  1. Anti-neurotrophic effects from autoantibodies in adult diabetes having primary open angle glaucoma or dementia

    Directory of Open Access Journals (Sweden)

    Mark B Zimering

    2013-05-01

    Full Text Available Aims: To test for anti-endothelial and anti-neurotrophic effects from autoantibodies in subsets of diabetes having open- angle glaucoma, dementia or control subjects.Methods: Protein-A eluates from plasma of 20 diabetic subjects having glaucoma or suspects and 34 age-matched controls were tested for effects on neurite outgrowth in rat pheochromocytoma PC12 cells or endothelial cell survival. The mechanism of the diabetic glaucoma autoantibodies' neurite inhibitory effect was investigated in coincubations with the selective Rho kinase inhibitor Y27632 or the sulfated proteoglycan synthesis inhibitor sodium chlorate. Stored protein-A eluates from certain diabetic glaucoma or dementia subjects which contained long-lasting, highly stable cell inhibitory substances were characterized using mass spectrometry and amino acid sequencing.Results: Diabetic primary open angle glaucoma or suspects (n=20 or diabetic dementia (n=3 autoantibodies caused significantly greater mean inhibition of neurite outgrowth in PC12 cells (p < .0001 compared to autoantibodies in control diabetic (n=24 or nondiabetic (n=10 subjects without glaucoma (p < .01. Neurite inhibition by the diabetic glaucoma autoantibodies was completely abolished by 10 µM concentrations of Y27632 (n=4. It was substantially reduced by 30 mM concentrations of sodium chlorate (n=4. Peak, long-lasting activity survived storage x 5 years at 0-4 deg C and was associated with a restricted subtype of Ig kappa light chain. Diabetic glaucoma or dementia autoantibodies (n=5 caused contraction and process retraction in quiescent cerebral cortical astrocytes effects which were blocked by 5 µM concentrations of Y27632. Conclusion: These data suggest that autoantibodies in adult diabetes having primary open angle glaucoma (glaucoma suspects and/or dementia inhibit neurite outgrowth and promote a reactive astrocyte morphology by a mechanism which may involve activation of the RhoA/p160 ROCK signaling pathway.

  2. The uptake of polluting chemicals into the plant and its relationship to physical-chemical substance properties

    International Nuclear Information System (INIS)

    The accumulation behaviour of 14C-labelled organic pollutants under laboratory and field conditions was investigated in spring barley and garden cress and evaluated in the light of a number of previously selected substance properties. The studies in the laboratory were restricted to one week, while those in the field were carried out over the entire growing season. They had the purpose of determining the accumulation of certain pollutants in the test plants with reference to the residues detected for those substances in the soil. The laboratory studies were focused on benzene and five chlorated derivatives as well as a further few chemicals from other groups of substances. The substances investigated in the field were benzene and an additional three chlorated benzenes. The accumulation of organic pollutants in the above-ground parts and roots of barley can rather easily be forecasted on the basis of the compounds' structural properties like molecular weight, molecule volume and connectivity indices. This applies to the majority of cases, providing the mineralisation of the substances in the soil is only minor and no unduly large amounts of metabolites are formed, the physical-chemical properties of which deviate greatly from those of the mother substances. Any such forecasts for cress should preferably be made on the basis of distribution parameters of the individual compounds. It was found that the results from laboratory and field studies were in reasonable agreement, thus permitting the same conclusions to be drawn as to the biotransfer of the test substances from the soil and the probable links between these observations and physical-chemical substance properties. (orig./MG)

  3. Preparation of polyferric chloride sulfate%聚合氯化硫酸铁制备方法

    Institute of Scientific and Technical Information of China (English)

    贾汝林

    2009-01-01

    聚合氯化硫酸铁是一种新型高效无机高分子水处理剂,其制备方法包括氯酸盐氧化法和氯气氧化法,即硫酸亚铁溶液在一定温度和酸度下与氯酸钠或液氯反应,生成一系列不同聚合度的聚铁溶液,温度、酸度和氧化剂都可影响其聚合度,不同产品用于水处理时效果也相差甚远.氯酸盐氧化法制备聚合氯化硫酸铁与氯气氧化法相比在成本和环保方面都占优,该方法代表了聚合氯化硫酸铁的工业生产方法.%Polyferric chloride sulfate (PFCS) is a new - type high - performance inorganic macromolecular water treatment agent.Its main preparation methods include chlorate oxidation method and chlorine oxidation method,namely ferrous sulfate solution react with sodium chlorate or liquid chlorine at a certain temperature and acidity to generate a series of PFCS solution with different polymerization degrees.Temperature,acidity,and oxidants can affect polymerization degree of the products and effect will differ greatly when they were used as water treatment agents.Compared with chlorine oxidation method,the other one is dominant in both terms of cost and environment protection,and it represents the industrial production method for PFCS.

  4. 草酸钠作为促染剂在活性黄3RS染色中的应用%Using Sodium Oxalate in the Dyeing of Cotton Fabric with Reactive Yellow 3 RS as an Accelerant

    Institute of Scientific and Technical Information of China (English)

    虞波; 周康; 胡文乾; 叶晓燕

    2015-01-01

    草酸盐作为光催化促进剂,在光化学反应中有着广泛的应用.研究了在活性黄3RS染棉织物过程中,草酸钠作为促染剂以取代无机盐(硫酸钠和氯化钠)的可行性,并将草酸钠与甲酸钠和柠檬酸钠等有机盐的促染效果进行了比较.结果显示草酸钠的促染效果优于甲酸钠、柠檬酸钠和氯化钠,与硫酸钠的促染效果相当.草酸钠作为促染剂,对染色织物的染色牢度和色光均没有影响.草酸钠可以取代无机盐,提高降解染色废水的光化学效果.%Sodium oxalate is used widely in the field of photochemical reaction as an accelerant. The feasibility of using sodium oxalate in the dyeing of cotton fabrics with reactive dyes in place of inorganic salt ( sodium sulfate or sodium chlorate) was studied. Meanwhile, the dyeing of cotton fabrics with reactive dyes using sodium formate and sodium citrate were investigated and the results obtained were compared with that of sodium oxalate. The re-sults show that the effect of sodium oxalate as an accelerant is better than that of sodium formate, sodium citrate and sodium chlorate, and its effect is equal to that of sodium sulfate. Sodium oxalate has no effect on the fastness and shade of the dyed fabric as an exhausting agent. Sodium oxalate could substitute for inorganic salt to enhance photochemical reaction of dyeing wastewater.

  5. Integrated Data Collection Analysis (IDCA) Program - AN and Bullseye Smokeless Powder

    Energy Technology Data Exchange (ETDEWEB)

    Sandstrom, Mary M. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Brown, Geoffrey W. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Preston, Daniel N. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Pollard, Colin J. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Warner, Kirstin F. [Naval Surface Warfare Center (NSWC), Indian Head, MD (United States); Sorensen, Daniel N. [Naval Surface Warfare Center (NSWC), Indian Head, MD (United States); Remmers, Daniel L. [Naval Surface Warfare Center (NSWC), Indian Head, MD (United States); Phillips, Jason J. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Shelley, Timothy J. [Bureau of Alcohol, Tobacco, and Firearms, Redstone Arsenal, AL (United States); Reyes, Jose A. [Applied Research Associates, Tyndall Air Force Base, FL (United States); Hsu, Peter C. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Reynolds, John G. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

    2013-07-17

    chlorate, sodium chlorate, sugar, dodecane, PETN, carbon, ammonium nitrate, Gunpowder, Bullseye® smokeless powder.

  6. 低成本靛蓝牛仔布氧化拔染印花工艺%Oxidative discharge printing process of denim fabric with low cost

    Institute of Scientific and Technical Information of China (English)

    朱瀛洲

    2013-01-01

      借鉴苯胺黑黑地防染印花工艺中的氯酸钠和黄血盐钾氧化组合,作为靛蓝氧化拔染剂,以柠檬酸为酸性介质,可以实现靛蓝牛仔布的氧化拔染印花,还可以用于靛蓝套染硫化染料或直接染料地色拔染印花等。生产中根据拔染效果和织物强力,可以调整氯酸钠和黄血盐钾用量和酸的用量,比商品靛蓝拔染剂如拔染剂C-100、拔染剂JN等更有优势,印花成本低,制浆采用冷法制备,简便快捷、汽蒸时间短、工艺条件可控、重现性好,能有效控制织物的强力损失。无甲醛使靛蓝拔染印花获得新生。%In view of the combination of sodium chlorate and yellow prussiate of potash used in black-based dye-resist printing process for aniline black as oxidative discharging agent, oxidative discharge printing of denim fabric can be realized through citric acid used as acidic medium. This kind combination can also be applied in the discharge printing based on sulfur dye or direct dye used with indigo. The dosage of sodium chlorate, yellow prussiate of potash and acid can be adjusted according to discharge effect and fabric strength in manufacture. It is superior to commercial discharging agents such as discharging agent C-100 and discharging agent JN due to low cost. The paste is prepared by cold method, which presented advantages as simpleness, rapidness, short steaming time, controlled technological conditions, good reproducibility and effective control the loss of fabric strength. Moreover, the formaldehyde-free process recreates indigo discharge printing.

  7. Construction, Characterization, and Animal Testing of WRSd1, a Shigella dysenteriae 1 Vaccine

    Science.gov (United States)

    Venkatesan, Malabi M.; Hartman, Antoinette B.; Newland, John W.; Ivanova, Vessela S.; Hale, Thomas L.; McDonough, Marie; Butterton, Joan

    2002-01-01

    WRSd1 is a Shigella dysenteriae 1 vaccine containing deletions of the virG(icsA) gene required for intercellular spreading and a 20-kb chromosomal region encompassing the Shiga toxin genes (stxAB). WRSd1 was constructed from S. dysenteriae 1 strain 1617 that was originally isolated during the 1968 to 1969 epidemic of Shiga dysentery in Guatemala. The virG(icsA) deletion was constructed from a streptomycin-resistant (Strr) mutant of 1617 by a filter mating procedures using a virG(icsA) deletion derivative, pΔvirG2. A colony that was invasive for HeLa cells and negative for the virG(icsA) gene by Southern blotting was grown anaerobically on plates containing chlorate for selection of resistant colonies that had lost the entire Shiga toxin gene. A virG(icsA) stxAB Strr mutant selected from the chlorate plates was designated WRSd1. This candidate vaccine was evaluated for safety, immunogenicity, and protective efficacy using the guinea pig keratoconjunctivitis model. WRSd1 was Sereny negative, and two applications of this strain to the cornea elicited a significant protective immune response against the S. dysenteriae 1 O antigen. Vaccination with WRSd1 conferred protection against challenge with each of three virulent S. dysenteriae 1 strains. Since a vaccine protecting against multiple Shigella species is required for most areas where Shigella is endemic, protection studies using a combination vaccine of Shigella sonnei vaccine strain WRSS1, Shigella flexneri 2a vaccine strain SC602, and WRSd1 were also performed. Guinea pigs vaccinated with a mixture of equal amounts of the three vaccine strains were protected against challenge with each of the homologous virulent strains. Unlike WRSS1 and SC602, however, the level of protection afforded by WRSd1 in a combination vaccine was lower than the protection elicited by a pure culture. A current Good Manufacturing Practice product of WRSd1 given intragastrically to rhesus monkeys proved safe and immunogenic. PMID:12010984

  8. 甘油合成1,3-丙二醇%Synthesis of 1,3-Propanediol from Glycerol

    Institute of Scientific and Technical Information of China (English)

    陈国辉; 孙全

    2011-01-01

    1,3-Propanediol was synthesized from glycerol by chloration,oxidation, Clemmensen reaction and hydrolysis. The structure of the target compound was determined by method of IR and MS. The molar ratio, temperature and solvent of the reaction were investigated to optimize the reaction conditions. The optimum conditions are: for chloration: 120 ℃; for oxidation: 23 ~ 27 ℃, n ( 1,3-dichloroacetone ): n ( sodium dichromate) = 1.8:1, the amount of reaction solvent: 1.4 g 1,3-dichloro-2-propanol per 1 mL water, and for Clemmensen reaction: n (1,3-dichloropropane): n ( zinc )= 1:1.2, with water as the desirable solvent, and the overall yield of 37. 1%.%以甘油为原料,经过氯代、氧化、克莱门森还原、水解4步反应,最终合成1,3-丙二醇,并用红外光谱仪和质谱仪对目标产物进行结构确定.从反应物摩尔比、反应温度、反应溶剂等优化了反应条件.最优反应条件为:氯代反应:温度120℃;氧化反应:温度23~27℃,,n(1,3-二氯-2-丙醇):n(重铬酸钠)=1.8:1,反应溶剂用量:1 mL水溶解1.4 g 1,3-二氯-2-丙醇;克莱门森还原反应:n(1,3-二氯丙酮):n(锌)=1:1.2,水作反应溶剂最佳,在该条件下,1,3-丙二醇总产率可达37.1%.

  9. Radiation chemical effects in the near-field environment of a radwaste repository: {gamma} radiolysis in 6 molal NaCl solutions; Strahlenchemische Effekte im Endlagernahbereich: {gamma}-Radiolyse in 6 molarer NaCl-Loesung

    Energy Technology Data Exchange (ETDEWEB)

    Kelm, M.; Bohnert, E.

    1997-12-01

    The radiation emitted from high-level radioactive wastes in a radwaste repository causes radiolysis products to be formed in brines resulting from water intrusion. The products may alter via redox and complexing reactions the mobilisation processes of radionuclides. The major products of {gamma} radiolysis determined in 6 molal NaCl solution as a function of radiation dose are hydrogen, oxygen, and chlorate. Hypochlorite and chlorite were found to have concentrations in the {mu}Mol/kg range. There was no dependence on dose rate. For the experiments under atmospheric pressure, which allowed radiolytic gas to escape from the solution, the G values measured are 0.46 (H{sub 2}), 0.16 (O{sub 2}), and 0.074 (ClO{sub 3}). In pressurized experiments, with radiolytic gas remaining contained in the solution, the radiolytic effect was much smaller. After approx. 100 days, at a dose of about 2 MGy, gas equilibrium concentrations of some mMol/kg were measured. The results can be qualitatively described by a system of parallel running reaction rate equations. As to quantitative analysis, the reaction model needs to be refined. (orig./CB) [Deutsch] Die Strahlung von hochradioaktiven Abfaellen in einem Endlager im Salz hat zur Folge, dass bei einem Wasserzutritt in den entstehenden Laugen Radiolyseprodukte gebildet werden. Die Radiolyseprodukte koennen durch Redox- und Komplexierungsreaktionen die Mobilisierbarkeit von Radionukliden veraendern. Als Hauptprodukte der {gamma}-Radiolyse wurden in 6 molaler NaCl-Loesung Wasserstoff, Sauerstoff und Chlorat in Abhaengigkeit von der Dosis bestimmt. Hypochlorit und Chlorit erreichten nur Konzentrationen im {mu}Mol/kg-Bereich. Eine Dosisleistungsabhaengigkeit war nicht festzustellen. Bei den Experimenten unter Normaldruck, bei denen die Radiolysegase aus der Loesung entweichen konnten, betrugen die G-Werte 0.46 (H{sub 2}), 0,16 (O{sub 2}) und 0,074 (ClO{sub 3}{sup -}). Bei den Experimenten unter Druck wurden die Radiolysegase in Loesung

  10. 尿样消化对尿碘检测结果质量的影响分析

    Institute of Scientific and Technical Information of China (English)

    闫向阳

    2013-01-01

    目的:探讨尿样消化对尿碘检测结果的影响。方法:随机选取20份尿检样品,采用氯酸消化法进行尿碘检测,采用两种不同质量的消化管进行尿样消化,观察两种消化管的消化结果,分析尿样消化对尿碘检测的影响。结果:消化管A尿碘检测质量优于消化管B,消化剩余酸量大于0.4ml或小于0.2ml,可见,消化温度及氯酸量是尿碘检测主要影响因素。结论:尿样消化温度需控制在110℃~115℃范围内,且氯酸量应为0.5ml,避免尿样消化对尿碘检测的影响。%Objective: to investigate the results of urine sample digestion for detecting urine iodine.Methods: randomly selected 20 samples of urine and chloric acid digestion method for urine iodine testing, using two different quality of digestive tube to carry on the urine sample digestion, observation of two kinds of digestive tube digestion as a result, the analysis of the effect of urine sample digestion for detecting urine iodine.Results: the digestive tube A urinary iodine testing quality is better than that of the digestive tube B, digesting residual acid amount is greater than 0.4 ml or less than 0.2 ml, visible, digestion temperature and quantity of chlorate are the main factors that influence the urine iodine testing.Conclusion: the urine sample digestion temperature to control within 110 ℃ ~ 115 ℃, and the amount of chlorate should be 0.5 ml, avoid the influence of the urine sample digestion for detecting urine iodine.

  11. Oxidative discharge printing process of denim fabric with low cost%低成本靛蓝牛仔布氧化拔染印花工艺

    Institute of Scientific and Technical Information of China (English)

    朱瀛洲

    2013-01-01

      借鉴苯胺黑黑地防染印花工艺中的氯酸钠和黄血盐钾氧化组合,作为靛蓝氧化拔染剂,以柠檬酸为酸性介质,可以实现靛蓝牛仔布的氧化拔染印花,还可以用于靛蓝套染硫化染料或直接染料地色拔染印花等。生产中根据拔染效果和织物强力,可以调整氯酸钠和黄血盐钾用量和酸的用量,比商品靛蓝拔染剂如拔染剂C-100、拔染剂JN等更有优势,印花成本低,制浆采用冷法制备,简便快捷、汽蒸时间短、工艺条件可控、重现性好,能有效控制织物的强力损失。无甲醛使靛蓝拔染印花获得新生。%In view of the combination of sodium chlorate and yellow prussiate of potash used in black-based dye-resist printing process for aniline black as oxidative discharging agent, oxidative discharge printing of denim fabric can be realized through citric acid used as acidic medium. This kind combination can also be applied in the discharge printing based on sulfur dye or direct dye used with indigo. The dosage of sodium chlorate, yellow prussiate of potash and acid can be adjusted according to discharge effect and fabric strength in manufacture. It is superior to commercial discharging agents such as discharging agent C-100 and discharging agent JN due to low cost. The paste is prepared by cold method, which presented advantages as simpleness, rapidness, short steaming time, controlled technological conditions, good reproducibility and effective control the loss of fabric strength. Moreover, the formaldehyde-free process recreates indigo discharge printing.

  12. Identification of inorganic improvised explosive devices by analysis of postblast residues using portable capillary electrophoresis instrumentation and indirect photometric detection with a light-emitting diode.

    Science.gov (United States)

    Hutchinson, Joseph P; Evenhuis, Christopher J; Johns, Cameron; Kazarian, Artaches A; Breadmore, Michael C; Macka, Miroslav; Hilder, Emily F; Guijt, Rosanne M; Dicinoski, Greg W; Haddad, Paul R

    2007-09-15

    A commercial portable capillary electrophoresis (CE) instrument has been used to separate inorganic anions and cations found in postblast residues from improvised explosive devices (IEDs) of the type used frequently in terrorism attacks. The purpose of this analysis was to identify the type of explosive used. The CE instrument was modified for use with an in-house miniaturized light-emitting diode (LED) detector to enable sensitive indirect photometric detection to be employed for the detection of 15 anions (acetate, benzoate, carbonate, chlorate, chloride, chlorite, cyanate, fluoride, nitrate, nitrite, perchlorate, phosphate, sulfate, thiocyanate, thiosulfate) and 12 cations (ammonium, monomethylammonium, ethylammonium, potassium, sodium, barium, strontium, magnesium, manganese, calcium, zinc, lead) as the target analytes. These ions are known to be present in postblast residues from inorganic IEDs constructed from ammonium nitrate/fuel oil mixtures, black powder, and chlorate/perchlorate/sugar mixtures. For the analysis of cations, a blue LED (470 nm) was used in conjunction with the highly absorbing cationic dye, chrysoidine (absorption maximum at 453 nm). A nonaqueous background electrolyte comprising 10 mM chrysoidine in methanol was found to give greatly improved baseline stability in comparison to aqueous electrolytes due to the increased solubility of chrysoidine and its decreased adsorption onto the capillary wall. Glacial acetic acid (0.7% v/v) was added to ensure chrysoidine was protonated and to enhance separation selectivity by means of complexation with transition metal ions. The 12 target cations were separated in less than 9.5 min with detection limits of 0.11-2.30 mg/L (calculated at a signal-to-noise ratio of 3). The anions separation system utilized a UV LED (370 nm) in conjunction with an aqueous chromate electrolyte (absorption maximum at 371 nm) consisting of 10 mM chromium(VI) oxide and 10 mM sodium chromate, buffered with 40 mM tris

  13. VLT/SINFONI Observations of Europa: New Insights into the Surface Composition

    Science.gov (United States)

    Ligier, N.; Poulet, F.; Carter, J.; Brunetto, R.; Gourgeot, F.

    2016-06-01

    We present new insights into Europa’s surface composition on the global scale from linear spectral modeling of a high spectral resolution data set acquired during a ground-based observation campaign using SINFONI4, an adaptive optics near-infrared instrument on the Very Large Telescope (ESO). The spectral modeling confirms the typical “bullseye” distribution of sulfuric acid hydrate on the trailing hemisphere, which is consistent with Iogenic sulfur ion implantation. However, the traditional hypothesis of the presence of sulfate salts on the surface of the satellite is challenged as Mg-bearing chlorinated species (chloride, chlorate, and perchlorate) are found to provide improved spectral fits. The derived global distribution of Mg-chlorinated salts (and particularly chloride) is correlated with large-scale geomorphologic units such as chaos and darker areas, thus suggesting an endogenous origin. Based on the 1.65 μm water-ice absorption band shape and position, the surface temperature is estimated to be in the range 110–130 K, and water ice is found to be predominantly in its crystalline state rather than amorphous. While amorphous water ice exhibits a strong correlation with the expected intensity of the Ionian plasma torus bombardment, crystalline water ice is instead more associated with distinct geomorphological units. Endogenous processes such as jets and ice heating due to active geology may explain this relationship. Otherwise, no evidence of a correlation between grain size for the water ice and the sputtering rate has been detected so far.

  14. Effects of low concentrations of bisulfite--sulfite and nitrite on microorganisms

    Energy Technology Data Exchange (ETDEWEB)

    Wodzinski, R.S.; Labeda, D.P.; Alexander, M.

    1978-04-01

    A wide range of microorganisms was tested to determine their sensitivity to low concentrations of bisulfite-sulfite and nitrite, solubility products of SO/sub 2/ and NO/sub 2/, respectively. Photosynthesis by blue-green algae (cyanobacteria) was more strongly inhibited by 0.1 mM bisulfite-sulfite and 1 mM nitrite at pH 6.0 than photosynthesis by eucaryotic algae and respiration of bacteria, fungi, and protozoa. At pH 7.7, blud-green algae were still more sensitive to busulfite-sulfite and nitrite than eurcaryotic algae, but the toxicity of bisulfite-sulfite and nitrite decreased as the pH increased. Photosynthesis by Anabaena flos-aquae at pH 6.0 was inhibited 25% by a bisulfite-sulfite concentration of 10 ..mu..M and 15% by a nitrite concentration of 50 ..mu..M. Photosynthesis by the blud-green alga, Lyngbya sp., was not exceptionally sensitive to chlorate and thiosulfate. Acetylene-reducing activity of Beijerinckia indica was completely inhibited by 0.1 mM bisulfite-sulfite at pH 4.0, the suppression being decreased with increasing pH.

  15. Organic acids and inorganic anions in Bayer liquors by ion chromatography after solid-phase extraction

    Institute of Scientific and Technical Information of China (English)

    ZHONG Fu-jin; CHEN Xiao-qing; ZHANG Shu-chao; LI Yue-ping

    2007-01-01

    A method for the simultaneous separation and determination of organic acids and inorganic anions in Bayer liquors was developed by gradient ion chromatography with suppressed conductivity detection. Formate, acetate, propionate, oxalate, succinate,glutarate, fluoride, chloride and sulfate were separated and determined in 33 min. The samples were pretreated with solid-phase extraction, which has high selectivity for removing a large number of metallic ions in the Bayer liquors, and filtered with a 0.45 μm filter membrane before being injected into the ion chromatographic system. The separation of six organic acids and three inorganic anions was achieved on an IonPac AS11-HC column with KOH as the eluent, and the detection was performed by a conductivity detection mode. No interference is found in the presence of fluorate, chlorate and sulphate when organic acids are determined. The calibration graphs of peak area for all the analytes are linear over a wide range. The relative standard derivation of the peak area of analytes is less than 2.14%. Under optimum conditions the detection ranges from 0.2 to 100.0 mg/L. The average recoveries of the added standards are between 94.3% and 102.8%.

  16. Cultivation and characterization of thermophilic Nitrospira species from geothermal springs in the US Great Basin, China, and Armenia.

    Science.gov (United States)

    Edwards, Tara A; Calica, Nicole A; Huang, Dolores A; Manoharan, Namritha; Hou, Weiguo; Huang, Liuqin; Panosyan, Hovik; Dong, Hailiang; Hedlund, Brian P

    2013-08-01

    Despite its importance in the nitrogen cycle, little is known about nitrite oxidation at high temperatures. To bridge this gap, enrichment cultures were inoculated with sediment slurries from a variety of geothermal springs. While nitrite-oxidizing bacteria (NOB) were successfully enriched from seven hot springs located in US Great Basin, south-western China, and Armenia at ≤ 57.9 °C, all attempts to enrich NOB from > 10 hot springs at ≥ 61 °C failed. The stoichiometric conversion of nitrite to nitrate, chlorate sensitivity, and sensitivity to autoclaving all confirmed biological nitrite oxidation. Regardless of origin, all successful enrichments contained organisms with high 16S rRNA gene sequence identity (≥ 97%) with Nitrospira calida. In addition, Armenian enrichments also contained close relatives of Nitrospira moscoviensis. Physiological properties of all enrichments were similar, with a temperature optimum of 45-50 °C, yielding nitrite oxidation rates of 7.53 ± 1.20 to 23.0 ± 2.73 fmoles cell(-1) h(-1), and an upper temperature limit between 60 and 65 °C. The highest rates of NOB activity occurred with initial NO2 - concentrations of 0.5-0.75 mM; however, lower initial nitrite concentrations resulted in shorter lag times. The results presented here suggest a possible upper temperature limit of 60-65 °C for Nitrospira and demonstrate the wide geographic range of Nitrospira species in geothermal environments. PMID:23528039

  17. Oxychlorine Detections on Mars: Implications for Cl Cycling

    Science.gov (United States)

    Sutter, B.; Jackson, W. A.; Ming, D. W.; Archer, P. D.; Stern, J. C.; Mahaffy, P. R.; Gellert, R.

    2016-01-01

    The Sample Analysis at Mars (SAM) instrument has detected evolved O2 and HCl indicating the presence of perchlorate and/or chlorate (oxychlorine) in all 11 sediments analyzed to date. The hyperarid martian climate is believed to have allowed accumulation of oxychlorine and assumed chloride contents similar to those in hyperarid terrestrial settings. The linear correlation of oxychlorine and chloride of Gale Crater sediments is low (r (sup 2) equals 0.64). Correlations present in hyperarid Antarctica and the Atacama Desert are attributed to unaltered atmospheric source coupled with minimal redox cycling by biological activity. Terrestrial semi-arid to arid settings have low correlations similar to Gale Crater and are attributed to additional inputs of Cl minus from sea salt, dust, and/or proximal playa settings, and possible reduction of oxychlorine phases during wetter periods. While microbiological processes could contribute to low oxychlorine/chloride correlations on Mars, several abiotic mechanisms are more likely, such as changing oxychlorine production rates with time and/or post-depositional geochemical redox processes that altered the Gale Crater oxychlorine and chloride contents.

  18. Isolation and preliminary characterization of a respiratory nitrate reductase from hydrocarbon-degrading bacterium Gordonia alkanivorans S7.

    Science.gov (United States)

    Romanowska, Irena; Kwapisz, Ewa; Mitka, Magdalena; Bielecki, Stanisław

    2010-06-01

    Gordonia alkanivorans S7 is an efficient degrader of fuel oil hydrocarbons that can simultaneously utilize oxygen and nitrate as electron acceptors. The respiratory nitrate reductase (Nar) from this organism has been isolated using ion exchange chromatography and gel filtration, and then preliminarily characterized. PAGE, SDS-PAGE and gel filtration chromatography revealed that Nar consisted of three subunits of 103, 53 and 25 kDa. The enzyme was optimally active at pH 7.9 and 40 degrees C. K(m) values for NO(3)(-) (110 microM) and for ClO(3)(-) (138 microM) were determined for a reduced viologen as an electron donor. The purified Nar did not use NADH as the electron donor to reduce nitrate or chlorate. Azide was a strong inhibitor of its activity. Our results imply that enzyme isolated from G. alkanivorans S7 is a respiratory membrane-bound nitrate reductase. This is the first report of purification of a nitrate reductase from Gordonia species.

  19. Derivation of the critical effect size/benchmark response for the dose-response analysis of the uptake of radioactive iodine in the human thyroid.

    Science.gov (United States)

    Weterings, Peter J J M; Loftus, Christine; Lewandowski, Thomas A

    2016-08-22

    Potential adverse effects of chemical substances on thyroid function are usually examined by measuring serum levels of thyroid-related hormones. Instead, recent risk assessments for thyroid-active chemicals have focussed on iodine uptake inhibition, an upstream event that by itself is not necessarily adverse. Establishing the extent of uptake inhibition that can be considered de minimis, the chosen benchmark response (BMR), is therefore critical. The BMR values selected by two international advisory bodies were 5% and 50%, a difference that had correspondingly large impacts on the estimated risks and health-based guidance values that were established. Potential treatment-related inhibition of thyroidal iodine uptake is usually determined by comparing thyroidal uptake of radioactive iodine (RAIU) during treatment with a single pre-treatment RAIU value. In the present study it is demonstrated that the physiological intra-individual variation in iodine uptake is much larger than 5%. Consequently, in-treatment RAIU values, expressed as a percentage of the pre-treatment value, have an inherent variation, that needs to be considered when conducting dose-response analyses. Based on statistical and biological considerations, a BMR of 20% is proposed for benchmark dose analysis of human thyroidal iodine uptake data, to take the inherent variation in relative RAIU data into account. Implications for the tolerated daily intakes for perchlorate and chlorate, recently established by the European Food Safety Authority (EFSA), are discussed. PMID:27268963

  20. 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.

  1. 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.

  2. Electrochemical disinfection using boron-doped diamond electrode--the synergetic effects of in situ ozone and free chlorine generation.

    Science.gov (United States)

    Rajab, Mohamad; Heim, Carolin; Letzel, Thomas; Drewes, Jörg E; Helmreich, Brigitte

    2015-02-01

    This work investigated the capability of using a boron-doped diamond (BDD) electrode for bacterial disinfection in different water matrices containing varying amounts of chloride. The feed water containing Pseudomonas aeruginosa was electrochemically treated while applying different electrode conditions. Depending on the applied current density and the exposure time, inactivation between 4- and 8-log of the targeted microorganisms could be achieved. The disinfection efficiency was driven by the generation of free chlorine as a function of chloride concentration in the water. A synergetic effect of generating both free chlorine and ozone in situ during the disinfection process resulted in an effective bactericidal impact. The formation of the undesired by-products chlorate and perchlorate depended on the water matrix, the applied current density and the desired target disinfection level. In case of synthetic water with a low chloride concentration (20 mg L(-1)) and an applied current density of 167 mA cm(-2), a 6-log inactivation of Pseudomonas aeruginosa could be achieved after 5 min of exposure. The overall energy consumption ranged between 0.3 and 0.6 kW h m(-3) depending on the applied current density and water chemistry. Electrochemical water disinfection represents a suitable and efficient process for producing pathogen-free water without the use of any chemicals.

  3. Consumers’ perception and knowledge of food safety: results of questionnaires accessible on IZSalimenTO website

    Directory of Open Access Journals (Sweden)

    Amaranta Traversa

    2015-04-01

    Full Text Available The present survey was undertaken to investigate consumers’ knowledge of the main foodborne agents and dietary regimen during pregnancy. Data were collected using monthly questionnaires available on IZSalimenTO website between March 2013 and January 2014. Hepatitis A virus questionnaire: 20 respondents (77% recognized berries as foodstuff linked to the outbreak of hepatitis A. The majority correctly indicated as precautionary advice to boil berries before consumption. Botulism questionnaire: 29 respondents (62% indicated pesto as food involved in botulism alert in July 2013. The risk of infant botulism in infant less than 1 year old due to honey consumption is known by 24 respondents (51%. Main foodborne disease questionnaire: the risk of infection by Salmonella after the consumption of foods made with raw eggs is known by the majority (94%; N=17 as well as the treatments to be applied in order to make fresh fish safe from parasites (76%. Pregnancy questionnaire: 20 respondents (74% believed that washing vegetables and fruits with sodium bicarbonate or chlorate solution is able to inactivate Toxoplasma; only 4 (15% reported both raw meat and vegetables washed with sodium bicarbonate as food at risk. Results indicate that all consumers should be trained on behaviour and dietary regimen to be adopted in pregnancy and in infant <1 year old. The website may be considered as a useful tool to assess consumers’ knowledge: both the news section and the contents published may be a source of information and education for consumers on food safety.

  4. Proton and deuterium NMR experiments in zero field

    International Nuclear Information System (INIS)

    High field solid-state NMR lineshapes suffer from inhomogeneous broadening since resonance frequencies are a function of molecular orientation. Time domain zero field NMR is a two-dimensional field-cycling technique which removes this broadening by probing the evolution of the spin system under zero applied field. The simplest version, the sudden transition experiment, induces zero field evolution by the sudden removal of the applied magnetic field. Theory and experimental results of this experiment and several variations using pulsed dc magnetic fuelds to initiate zero field evolution are presented. In particular, the pulsed indirect detection method allows detection of the zero field spectrum of one nuclear spin species via another (usually protons) by utilizing the level crossings which occur upon adiabatic demagnetization to zero field. Experimental examples of proton/deuteron systems are presented which demonstrate the method results in enhanced sensitivity relative to that obtained in sudden transition experiments performed directly on deuterium. High resolution 2H NQR spectra of a series of benzoic acid derivatives are obtained using the sudden transition and indirect detection methods. Librational oscillations in the water molecules of barium chlorate monohydrate are studied using proton and deuterium ZF experiments. 177 refs., 88 figs., 2 tabs

  5. 不同浓度下四种除草剂对福寿螺和坑螺的生态毒理效应%Eco-toxicological effects of four herbicides on typical aquatic snail Pomacea canaliculata and Crown conchs

    Institute of Scientific and Technical Information of China (English)

    赵兰; 骆世明; 黎华寿; 贺鸿志; 陈桂葵; 秦俊豪

    2011-01-01

    以化学除草剂应用为前提的水稻免耕抛秧栽培技术是近年来推广的节本栽培新技术.为更好地评价除草剂的环境风险,为防治除草剂的负效应提供科学依据,采用室内静水模拟实验研究了4种免耕稻田除草剂丁草胺、苄嘧N磺隆、丁苄混剂和氯酸钾的3种浓度梯度下对典型水生动物福寿螺、坑螺的影响.结果表明,各除草剂对水生动物的代谢都有不同程度的影响,氯酸钾和苄嘧磺隆对2种水生动物的呼吸作用影响不大,而丁草胺和丁苄混剂对3种水生动物的呼吸作用的影响有显著的抑制作用,且呈现一定的剂量效应;在本实验染毒剂量下,丁草胺和丁苄混剂对2种水生动物的存活率影响很大,而氯酸钾和苄嘧磺隆对其存活率影响较小.丁草胺和丁苄混剂处理对福寿螺的氮代谢影响远远大于氯酸钾和苄嘧磺隆处理,而从水体总氮和总磷含量的影响来看,4种除草剂对其影响都较大.总之,从4种除草剂对实验用螺存活率和主要代谢生理指标的综合影响大小来看,丁草胺>丁苄混剂>苄嘧磺隆>氯酸钾.%There has been an increase in the use of other herbicides for both agricultural and non-agricultural purposes. The use of herbicides in China also has increased faster than that of insecticides and fungicides since last 30 years. The new technique of rice seedling-broadcasting with no-tillage ( RSB-NT) is widely used and it was based on the applition of herbicides. The increasing pollution of herbicides in soil and water has been of concerns. The effect of four herbicides including butachlor, bensulfuron-methyl, the mixture of bensulfuron and butachlor, potassium chlorate on typical aquatic animals (Pomacea canaliculata Spix, Tunnel snail) in rice paddy wetland were studied in laboratory. In the immersion experiment, both of the aquatic animals divided into four groups with three concentrations. The results showed that the

  6. Comparison of Bacillus atrophaeus spore viability following exposure to detonation of C4 and to deflagration of halogen-containing thermites

    Energy Technology Data Exchange (ETDEWEB)

    Tringe, J. W.; Létant, S. E.; Dugan, L. C.; Levie, H. W.; Kuhl, A. L.; Murphy, G. A.; Alves, S. W.; Vandersall, K. S. [Lawrence Livermore National Laboratory, 7000 East Avenue, Livermore, California 94550 (United States); Pantoya, M. L. [Mechanical Engineering Department, Texas Tech University, Lubbock, Texas 79409 (United States)

    2013-12-21

    Energetic materials are being considered for the neutralization of spore-forming bacteria. In this study, the neutralization effects of a monomolecular explosive were compared to the effects of halogen-containing thermites. Bacillus atrophaeus spores were exposed to the post-detonation environment of a 100 g charge of the military explosive C-4 at a range of 50 cm. These tests were performed in the thermodynamically closed environment of a 506-l barometric calorimeter. Associated temperatures were calculated using a thermodynamic model informed by calculations with the Cheetah thermochemical code. Temperatures in the range of 2300–2800 K were calculated to persist for nearly the full 4 ms pressure observation time. After the detonation event, spores were characterized using optical microscopy and the number of viable spores was assessed. Results showed live spore survival rates in the range of 0.01%–1%. For the thermite tests, a similar, smaller-scale configuration was employed that examined the spore neutralization effects of two thermites: aluminum with iodine pentoxide and aluminum with potassium chlorate. Only the former mixture resulted in spore neutralization. These results indicate that the detonation environment produced by an explosive with no chemical biocides may provide effective spore neutralization similar to a deflagrating thermite containing iodine.

  7. 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.

  8. Influence of electrolytes (TEABF4 and TEMABF4) on electrochemical performance of graphite oxide derived from needle coke.

    Science.gov (United States)

    Yang, Sunhye; Kim, Ick-Jun; Choi, In-Sik; Bae, Mi-Kyeong; Kim, Hyun-Soo

    2013-05-01

    The structure of needle coke was changed to graphite oxide structure after oxidation treatment with 70 wt.% of nitric acid and sodium chlorate (NaClO3), and the inter-layer distance of the oxidized needle coke was expanded to 6.9 angstroms. The first charge profile of the oxidized needle coke-cell with 1.2 M TEMABF4/acetonitrile solution displayed that the intercalation of electrolyte ions into the inter-layer occurred at 1.0 V, which value is lower than 1.3 V of the oxidized needle coke-cell with 1.2 M TEABF4/acetonitrile solution. After first charge/discharge, the cell using TEMABF4 electrolyte exhibited smaller electrode resistance of 0.05 omega, and larger specific volume capacitance of 25.5 F/ml at the two-electrode system in the potential range 0-2.5 V than those of the cell using TEABF4 electrolyte. Compared to the TEABF4 electrolyte, better electrochemical performance of the TEMABF4 electrolyte in the oxidized needle coke may be caused by the smaller cation (TEMA+) size and better ion mobility in the nanopores between inter-layers. PMID:23858941

  9. Enthalpy-driven interactions with sulfated glycosaminoglycans promote cell membrane penetration of arginine peptides.

    Science.gov (United States)

    Takechi-Haraya, Yuki; Nadai, Ryo; Kimura, Hitoshi; Nishitsuji, Kazuchika; Uchimura, Kenji; Sakai-Kato, Kumiko; Kawakami, Kohsaku; Shigenaga, Akira; Kawakami, Toru; Otaka, Akira; Hojo, Hironobu; Sakashita, Naomi; Saito, Hiroyuki

    2016-06-01

    The first step of cell membrane penetration of arginine peptides is thought to occur via electrostatic interactions between positive charges of arginine residues and negative charges of sulfated glycosaminoglycans (GAGs) on the cell surface. However, the molecular interaction of arginine peptides with GAG still remains unclear. Here, we compared the interactions of several arginine peptides of Tat, R8, and Rev and their analogues with heparin in relation to the cell membrane penetration efficiency. The high-affinity binding of arginine peptides to heparin was shown to be driven by large favorable enthalpy contributions, possibly reflecting multidentate hydrogen bondings of arginine residues with sulfate groups of heparin. Interestingly, the lysine peptides in which all arginine residues are substituted with lysine residues exhibited negligible binding enthalpy despite of their considerable binding to heparin. In CHO-K1 cells, arginine peptides exhibited a great cell-penetrating ability whereas their corresponding lysine peptides did not penetrate into cells. The degree of cell penetration of arginine peptides markedly decreased by the chlorate treatment of cells which prevents the sulfation of GAG chains. Significantly, the cell penetration efficiency of arginine peptides was found to be correlated with the favorable enthalpy of binding to heparin. These results suggest that the enthalpy-driven strong interaction with sulfated GAGs such as heparan sulfate plays a critical role in the efficient cell membrane penetration of arginine peptides.

  10. Entamoeba mitosomes play an important role in encystation by association with cholesteryl sulfate synthesis.

    Science.gov (United States)

    Mi-ichi, Fumika; Miyamoto, Tomofumi; Takao, Shouko; Jeelani, Ghulam; Hashimoto, Tetsuo; Hara, Hiromitsu; Nozaki, Tomoyoshi; Yoshida, Hiroki

    2015-06-01

    Hydrogenosomes and mitosomes are mitochondrion-related organelles (MROs) that have highly reduced and divergent functions in anaerobic/microaerophilic eukaryotes. Entamoeba histolytica, a microaerophilic, parasitic amoebozoan species, which causes intestinal and extraintestinal amoebiasis in humans, possesses mitosomes, the existence and biological functions of which have been a longstanding enigma in the evolution of mitochondria. We previously demonstrated that sulfate activation, which is not generally compartmentalized to mitochondria, is a major function of E. histolytica mitosomes. However, because the final metabolites of sulfate activation remain unknown, the overall scheme of this metabolism and the role of mitosomes in Entamoeba have not been elucidated. In this study we purified and identified cholesteryl sulfate (CS) as a final metabolite of sulfate activation. We then identified the gene encoding the cholesteryl sulfotransferase responsible for synthesizing CS. Addition of CS to culture media increased the number of cysts, the dormant form that differentiates from proliferative trophozoites. Conversely, chlorate, a selective inhibitor of the first enzyme in the sulfate-activation pathway, inhibited cyst formation in a dose-dependent manner. These results indicate that CS plays an important role in differentiation, an essential process for the transmission of Entamoeba between hosts. Furthermore, we show that Mastigamoeba balamuthi, an anaerobic, free-living amoebozoan species, which is a close relative of E. histolytica, also has the sulfate-activation pathway in MROs but does not possess the capacity for CS production. Hence, we propose that a unique function of MROs in Entamoeba contributes to its adaptation to its parasitic life cycle.

  11. Evaluation of the sensitivity of three sublethal cytotoxicity assays in human HepG2 cell line using water contaminants

    International Nuclear Information System (INIS)

    The in vitro toxicological index IC50 (the millimolar concentration of compound which inhibits response assay by 50% compared to the solvent control) of 11 water contaminants (acrylamide, atrazine, B[a]P, BPA, 2,4-DAT, 17-αEE, H2O2, 4-OP, sodium bromate, sodium chlorate, sodium nitrate) was evaluated on the human hepatoma (HepG2) cells using three short-term bioassays related to their morbidity status [radiometric RNA synthesis assay (RNA), luminometric ATP assay (ATP), fluorometric Alamar blue assay (AB)]. Among all substances, we were not able to determine atrazine IC50 value whatever the test used. Furthermore, B[a]P was not cytotoxic in the ATP and AB assays. Statistical analysis revealed a correlation between the IC50 values obtained in the three assays. Except with 4-OP, RNA assay was always inhibited at lower concentrations than those required in the other assays, suggesting that this assay is a very sensitive indicator of the presence of toxic compounds. ATP and AB assays responded to a similar pattern. Due to its higher sensitivity and its reliability, RNA synthesis assay using HepG2 cell line provides the most suitable tool for the screening of water contaminants

  12. A new method for oxidation of gaseous, elemental mercury.

    Energy Technology Data Exchange (ETDEWEB)

    Livengood, C. D.; Mendelsohn, M. H.

    1999-08-23

    Elemental mercury (Hg) is difficult to remove from flue-gas streams using existing wet-scrubber technology, primarily because of its limited volubility in water. We have proposed and tested a concept for enhancing gaseous Hg{sup 0}removal in wet scrubber systems by altering the chemical form of the Hg{sup 0} to a water-soluble oxidized species. Recently, we have discovered a new method for injection of the oxidizing species that dramatically improves reactant utilization and at the same time gives significant nitric oxide (NO) oxidation as well. Our method uses a diluted oxidizing solution containing chloric acid and sodium chlorate (sold commercially as NOXSORB{trademark}). When this solution is injected into a gas stream containing Hg{sup 0} at about 300 F, we found that nearly 100% of the Hg{sup 0} was removed from the gas phase and was recovered in liquid samples from the test system. At the same time, approximately 80% of the added NO was also removed (oxidized). The effect of sulfur dioxide (SO{sub 2}) on this method was also investigated, and it appears to decrease slightly the amount of Hg oxidized. We are currently testing the effect of variations in oxidizing solution concentration, SO{sub 2} concentration, NO concentration, and reaction time (residence time).

  13. PLA-b-PEG/magnetite hyperthermic agent prepared by Ugi four component condensation

    Directory of Open Access Journals (Sweden)

    L. P. Icart

    2016-03-01

    Full Text Available Ugi four component condensation (UFCC, is an important tool for the synthesis of different types of bioconjugate species. In this study, a PLA-PEG/magnetite magnetic composite was prepared by a synthetic-route approach based on UFCC. In particular, poly(lactic acid (PLA was synthesized by autocatalytic polycondensation. Also, poly(ethyleneglycol bis-amine (bis-amine PEG was synthesized by two different methods: via carbonyldiimidazol (CDI/ethylenediamine (ED (75% yield and via chlorate monochlorated acetyl (CCA/ED (95% yield. All products were characterized by gel permeation chromatography (GPC, hydrogen-1 nuclear magnetic resonance (NMR 1H, Fourier transform infrared (FTIR, differential scanning calorimetry (DSC and thermogravimetric analysis (TGA. In addition, magnetite was prepared and modified to generate aldehyde groups which are also necessary for UFCC. This product was characterized by DSC, TGA, X-ray diffraction (XRD and magnetic force (MF techniques. Also, the magnetic composite PLA-PEG/magnetite was synthesized by UFCC. The calculated yield was equal to 80%. Furthermore, magnetic microspheres were prepared by the procedure of emulsion solvent-evaporation and characterized by scanning electron microscopy (SEM and magnetic induction hyperthermia (MIH. The main contribution of these results is to propose a new application for UFCC in the preparation of biomasked magnetic drug delivery systems able to improve the cancer treatment and even the welfare of the patients.

  14. Canadian Occidental Petroleum Ltd. 1998 annual report

    International Nuclear Information System (INIS)

    Financial information from Canadian Occidental Petroleum Ltd. and a review of their 1998 operations was made available for the benefit of shareholders. The company's core oil and gas business activities include exploration, development, production and marketing of crude oil and natural gas. The company produces oil and gas in Canada, Yemen, the Gulf of Mexico and Nigeria. Canadian Occidental also owns a 7.23 per cent share in the Syncrude joint venture. The company is developing new production in Hay, British Columbia, offshore west Africa and offshore northwest Australia. They are also one of North America's top three manufacturers of sodium chlorate. The report presents a summary of operations, a thorough management discussion and analysis of results and provides the customary consolidated financial statements and notes. Overall, 1998 was described as a difficult year financially, due to falling commodity prices. On the operations side, the company experienced its best results to date, producing more oil and gas than ever before. The company also invested over $ 950 million in new projects and opportunities. Some of the Company's most promising projects are located offshore Nigeria, offshore northwest Australia, in the Gulf of Mexico and in western Canada. These projects are expected to add 40,000 BOE of production by early 2000, with promise of attractive returns even at current low oil prices. tabs., figs

  15. Recovery of Co(Ⅱ) and Ni(Ⅱ) from hydrochloric acid solution of alloy scrap

    Institute of Scientific and Technical Information of China (English)

    SHEN Yong-feng; XUE Wen-ying; NIU Wen-yong

    2008-01-01

    A hydrometallurgical process was developed for recovery of nickel and cobalt from the hydrochloric acid leaching solution of alloy scraps. The process consists of five major unit operations: 1) leaching with 6 mol/L hydrochloric acid under the L/S ratio of 10:1 at 95 ℃ for 3 h; 2) copper replacement by iron scraps under pH value of 2.0 at 80 ℃, and stirring for 1 h; 3) removal of iron and chromium by chemical precipitation: iron removal under pH value of 2.0 at 90 ℃ by dropwise addition of sodium chlorate and 18% sodium carbonate solution, then chromium removal under pH value of 4.0 at 70 ℃ by addition of nickel carbonate solution, stirred by air flow for 2 h; 4) selective separation of cobalt from nickel by extraction using 30% trialkyl amine+50% kerosene (volume fraction) and tri-n-butylphosphate (TBP) as a phase modifier with the O/A ratio of 2:1, and stripping of cobalt with 0.01 mol/L HC1; 5) crystallization of nickel chloride and electrodeposition of cobalt. It is found that the nickel recovery of 95% and the cobalt recovery of approximately 60% with purity over 99.9% are obtained by this process.

  16. Synthesis,Crystal Structure and Electrochemical Properties of a One-dimensional Chain Coordination Polymer[Cu(phen)(2,4,6-TMBA)2(H2O)]n

    Institute of Scientific and Technical Information of China (English)

    LI Wei; LI Chang-Hong; YANG Ying-Qun; KUANG Yun-Fei

    2008-01-01

    A one-dimensional chain coordination polymer[Cu(phen)(2,4,6-TMBA)2(H2O)]n has been synthesized by reacting 2,4,6-trimethyl-benzoic acid,1,10-phenanthroline and Cu(Ⅱ)per-chlorate and its structure Was characterized.Crystal data for this complex:tetragonal,space group I41,a=2.0293(3),b=2.0293(3),c=113758(2)nm,a=β=γ=90°,V=5.6657(13)nm3,Dc=1.379g/cm3,Z=8,μ(MoKa)=0.815mm-1,Mr=588.14,F(000)=2456,S=1.047,R=0.0459 and wR=O.1053.The crystal structure shows that two neighboring Cu(Ⅱ)ions are linked together by one bridging-chelating 2,4,6-trimethyl-benzoic group,forming a one-dimensional chain structure.Each Cu(Ⅱ)ion is coordinated with two nitrogen atoms from one 1,10-phenanthroline molecule,three oxygen atoms from three 2,4,6-trimethyl-benzoic acid molecules and one oxygen atom from one water molecule,giving a six-coordinate distorted octahedral coordination geometry.The cyclic voltamrnetry behavior of the complex was also investigated.

  17. Water-miscible cooling lubricants - determination of anorganic anions and carboxylic acids using capillary zone electrophoresis; Wassermischbare Kuehlschmierstoffe - Bestimmung von anorganischen Anionen und Carbonsaeuren mittels der Kapillarzonenelektrophorese

    Energy Technology Data Exchange (ETDEWEB)

    Schubert, B.A. [Fachbereich 8, Analytische Chemie II, Universitaet-GH Siegen (Germany); Dengel, H.S. [Fachbereich 8, Analytische Chemie II, Universitaet-GH Siegen (Germany); Hohaus, E. [Fachbereich 8, Analytische Chemie II, Universitaet-GH Siegen (Germany); Maurer, W. [Fachbereich 8, Analytische Chemie II, Universitaet-GH Siegen (Germany); Riepe, W. [Fachbereich 13, Analytische Chemie, Universitaet-GH Paderborn (Germany)

    1997-07-01

    A procedure is presented which allows the quantitative determination for most of the essentiell inorganic anions besides several carbonic acids (oxalic-, citric-, malonic-, tartaric-, formic-, succinic- and adipinic acid) in concentrates and industrial application emulsions of watermiscible cooling lubricants either free of mineral oil or oleiferous. The method used is based on capillary zones electrophoresis (CZE) using indirect UV-detection. The quantification of these substances regarding a qualiy surveillance of lubricants for manufacturers and a control of possible toxicological infleunces in working places is easily performed in spite of the complex matrix of the lubricants. Only a simple dilution is necessary. Analytical chemcial parameters such as accuracy, precision and recovery rate for concentrates and emulsions in industrial use for 1995/96 reveal sufficient universal application of the presented method for general purpose analyzing cooling lubricants. (orig.) [Deutsch] Es wird ein Verfahren vorgestellt, mit dem in Konzentraten und Emulsionen von wassermischbaren mineraloelfreien und mineraloelhaltigen Kuehlschmierstoffen (KSS) neben den wesentlichen anorganischen Anionen (Thiosulfat, Bromid, Chlorid, Sulfat, Nitrit, Nitrat, Perchlorat, Chlorat, Phosphonat, Fluorid, Phosphat) Carbonsaeuren (Oxal-, Citronen-, Malon-, Wein-, Ameisen-, Bernstein- und Adipinsaeure) mit Hilfe der Kapillarzonenelektrophorese (CZE) und indirekter UV-Detektion quantitativ bestimmt werden koennen. Die Quantifizierung dieser Substanzen im Rahmen von Qualitaetssicherungs- und Arbeitsschutzmassnahmen in KSS ist trotz der komplexen Matrix der KSS ohne eine aufwendige Probenvorbereitung moeglich. Ein einfacher Verduennungsschritt der Proben genuegt. Die analytischen Verfahrenskenngroessen Richtigkeit, Praezision, Wiederfindung sowie die Untersuchungsergebnisse fuer KSS-Konzentrate einiger Hersteller aus den Produktionsjahren 1995/96 werden vorgestellt. (orig.)

  18. Kinetics study of leaching arsenic from Ni-Mo ore roasting in dust mixture of hydrochloric and sulfuric acids

    Institute of Scientific and Technical Information of China (English)

    侯晓川; 杨润德; 李贺; 曾理; 肖连生

    2014-01-01

    The kinetics of leaching arsenic from Ni-Mo ore roasting dust was investigated. The effects including leaching temperature, particle size of the smelter dust, stirring speed, the coefficientβ(the molar ratio of sodium chlorate to arsenic in the smelter dust) and the initial H+ concentration on leaching arsenic were studied. The results indicate that the leaching of arsenic increases sharply with the decrease of particle size. The orders of reaction with respect to H+ concentration and particle size are determinted to be 1.136 and-1.806, respectively.The leaching of arsenic reaches 99% under experimental conditions, the apparent activation energy is determined to be 11.157 kJ/mol, which is consistent with the values of activation energy for diffusion model. The kinetics equation of leaching arsenic from the roasting dust could be expressed by a semi-empirical equation as 1-2/3η-(1-η)2/3=k0(c[H+])1.136r0-1.806exp[(-11157/RT)t].

  19. Vanadium recovery from clay vanadium mineral using an acid leaching method

    Institute of Scientific and Technical Information of China (English)

    LI Haoran; FENG Yali; LIANG Jianglong; LUO Xiaobing; DU Zhuwei

    2008-01-01

    A technique including direct acid leaching,vanadium precipitation with alkaline,sodium hydroxide releaching,impurity removing by adjusting pH value,precipitation vanadium with ammonium chloride,and vanadium pentoxide by roasting steps was proposed according to the characteristic of Xichuan clay vanadium mineral.The factors influencing leaching vanadium such as temperature and the concentration of sulfuric acid were investigated and optimized.The experimental results indicate that the extract ratios of V2O5 can reach 94% and 92% at a sodium chlorate ratio of 3% and a manganese dioxide ratio of 3%,respectively.A completely chemical precipitation method was adopted to decontaminate and enrich the vanadium in the acid leaching solution.The X-ray diffraction (XRD) pattern and the purity analysis of vanadium pentoxide indicate that the purity of final vanadium pentoxide can reach 99% and meet the standard specifications.The total recovery can reach about 75%.The technique has the characteristics of simplicity,less investlnent,and more environment safety as compared with the traditional salt roasting method.

  20. Preparation and magnetic properties of CoFe2O4/TiO2 composite films

    Institute of Scientific and Technical Information of China (English)

    TIAN XiaoXia; QU ShaoBo; PEI ZhiBin; WANG BinKe

    2008-01-01

    Using (Ti(OC4H9)4) and metal chlorates as starting materials, CoFe2O4/TiO2 composite films were pre-pared by sol-gel method. The effects of heat treatment temperature and pH of the precursor on micro-structure and magnetic properties were studied. The phase structure of the samples was examined by X-ray diffraction. The microstructure was examined by scanning electron microscope, atomic force microscope and polarized microscope. The magnetic property was measured by vibrating sample magnetometer. The results show that the crystals of different phases grow up independently. CoFe2O4 is uniformly embedded into the TiO2 matrix in the prepared composite films, and the growth of com-posite films is dependent on the heat treatment temperatures and PH of the precursor. The average size of CoFe2O4 crystal is 19 nm in Nanocomposite film prepared when the heat treatment temperature is 800℃ and the pH of the precursor is between 2 and 3. The magnetism of the composite films is en-hanced as the heat treatment temperature increases.

  1. 用于空间站火灾防护的隔绝式氧烛呼吸自救器研制%Study of oxygen candle's self-contained breathing rescuer against space station fire

    Institute of Scientific and Technical Information of China (English)

    周兴明; 胡晓; 毛胜华; 毛龙; 张毅; 陈淑娟

    2013-01-01

    A breathing self-rescuer is designed for fire escape in manned spacecraft. Its new self-contained breathing protecting device is composed of hood, sodium chlorate oxygen candle and CO2 absorbing part. The Venturi tube drives the air cycling with the oxygen produced by the oxygen candle, and the Lithium hydroxide absorbs CO2. The device went through human tests and was found comfortable. The possible use of the self-rescuer against space station fire is discussed. It is concluded that the oxygen candle's self-contained rescuer can be used for the fire escape in manned spacecraft.%文章介绍某新型隔绝式氧烛呼吸自救器的研制.其呼吸保护装置主要由防护头罩、氯酸钠氧烛和CO2吸附3个单元组成,利用氧烛产生的O2通过文丘里管推动头罩内的空气循环,采用LiOH吸附剂吸附循环气体中的CO2.该装置进行了适用性试验,人体感觉良好.文章对该装置用于空间站火灾逃生自救的可行性进行了分析,认为其适用于空间站火灾逃生.

  2. On the suppression of cathodic hypochlorite reduction by electrolyte additions of molybdate and chromate ions

    Directory of Open Access Journals (Sweden)

    JOHN GUSTAVSSON

    2012-11-01

    Full Text Available The goal of this study was to gain a better understanding of the feasibility of replacing Cr(VI in the chlorate process by Mo(VI, focusing on the cathode reaction selectivity for hydrogen evolution on steel and titanium in a hypochlorite containing electrolyte. To evaluate the ability of Cr(VI and Mo(VI additions to hinder hypochlorite reduction, potential sweep experiments on rotating disc electrodes and cathodic current efficiency (CE measurements on stationary electrodes were performed. Formed electrode films were investigated with scanning electron microscopy and energy-dispersive X-ray spectroscopy. Cathodic hypochlorite reduction is hindered by the Mo-containing films formed on the cathode surface after Mo(VI addition to the electrolyte, but much less efficient compared to Cr(VI addition. Very low levels of Cr(VI, in the mM range, can efficiently suppress hypochlorite reduction on polished titanium and steel. Phosphate does not negatively influence the CE in the presence of Cr(VI or Mo(VI but the Mo-containing cathode films become thinner if the electrolyte during the film build-up also contains phosphate. For a RuO2-TiO2 anode polarized in electrolyte with 40 mM Mo(VI, the anode potential increased and increased molybdenum levels were detected on the electrode surface

  3. A study of the effects of solid phase reactions on the thermal degradation and ballistic properties of solid propellants

    Science.gov (United States)

    Schmidt, W. G.

    1974-01-01

    The thermal stability of perchlorate composite propellants was studied at 135 and 170 C. The experimental efforts were concentrated on determining the importance of heterogeneous oxidizer-fuel reactions in the thermal degradation process. The experimental approach used to elucidate the mechanisms by which the oxidizer fuel composites thermally degrade was divided into two parts: (1) keeping the fuel constant and varying the nature of the oxidizers, and (2) holding the oxidizer constant and varying the fuel components. The fuel component primarily utilized in the first phase was polyethylene. Oxidizers included KClO4, KClO3, NH4ClO4 and NH4ClO4 doped with materials such as chlorate, phosphate and arsenate. In the second phase the oxidizer used was primarily NH4ClO4 while the fuels included saturated and unsaturated polybutadiene prepolymers and a series of bonding agents. Techniques employed in the current study include thermogravimetric measurements, differential thermal analysis, infrared, mass spectrometry, electron microscopy, and appropriate wet chemical analysis.

  4. Glycosaminoglycans in human retinoblastoma cells: Heparan sulfate, a modulator of the pigment epithelium-derived factor-receptor interactions

    Science.gov (United States)

    Alberdi, Elena M; Weldon, John E; Becerra, S Patricia

    2003-01-01

    Background Pigment epithelium-derived factor (PEDF) has binding affinity for cell-surface receptors in retinoblastoma cells and for glycosaminoglycans. We investigated the effects of glycosaminoglycans on PEDF-receptor interactions. Results 125I-PEDF formed complexes with protease-resistant components of medium conditioned by human retinoblastoma Y-79 cells. Using specific glycosaminoglycan degrading enzymes in spectrophotometric assays and PEDF-affinity chromatography, we detected heparin and heparan sulfate-like glycosaminoglycans in the Y-79 conditioned media, which had binding affinity for PEDF. The Y-79 conditioned media significantly enhanced the binding of 125I-PEDF to Y-79 cell-surface receptors. However, enzymatic and chemical depletion of sulfated glycosaminoglycans from the Y-79 cell cultures by heparitinase and chlorate treatments decreased the degree of 125I-PEDF binding to cell-surface receptors. Conclusions These data indicate that retinoblastoma cells secrete heparin/heparan sulfate with binding affinity for PEDF, which may be important in efficient cell-surface receptor binding. PMID:12625842

  5. The contribution of mediated oxidation mechanisms in the electrolytic degradation of cyanuric acid using diamond anodes.

    Science.gov (United States)

    Bensalah, Nasr; Dbira, Sondos; Bedoui, Ahmed

    2016-07-01

    In this work, the contribution of mediated oxidation mechanisms in the electrolytic degradation of cyanuric acid using boron-doped diamond (BDD) anodes was investigated in different electrolytes. A complete mineralization of cyanuric acid was obtained in NaCl; however lower degrees of mineralization of 70% and 40% were obtained in Na2SO4 and NaClO4, respectively. This can be explained by the nature of the oxidants electrogenerated in each electrolyte. It is clear that the contribution of active chlorine (Cl2, HClO, ClO(-)) electrogenerated from oxidation of chlorides on BDD is much more important in the electrolytic degradation of cyanuric acid than the persulfate and hydroxyl radicals produced by electro-oxidation of sulfate and water on BDD anodes. This could be explained by the high affinity of active chlorine towards nitrogen compounds. No organic intermediates were detected during the electrolytic degradation of cyanuric acid in any the electrolytes, which can be explained by their immediate depletion by hydroxyl radicals produced on the BDD surface. Nitrates and ammonium were the final products of electrolytic degradation of cyanuric acid on BDD anodes in all electrolytes. In addition, small amounts of chloramines were formed in the chloride medium. Low current density (≤10mA/cm(2)) and neutral medium (pH in the range 6-9) should be used for high efficiency electrolytic degradation and negligible formation of hazardous chlorate and perchlorate. PMID:27372125

  6. Comparison of Bacillus atrophaeus spore viability following exposure to detonation of C4 and to deflagration of halogen-containing thermites

    Science.gov (United States)

    Tringe, J. W.; Létant, S. E.; Dugan, L. C.; Levie, H. W.; Kuhl, A. L.; Murphy, G. A.; Alves, S. W.; Vandersall, K. S.; Pantoya, M. L.

    2013-12-01

    Energetic materials are being considered for the neutralization of spore-forming bacteria. In this study, the neutralization effects of a monomolecular explosive were compared to the effects of halogen-containing thermites. Bacillus atrophaeus spores were exposed to the post-detonation environment of a 100 g charge of the military explosive C-4 at a range of 50 cm. These tests were performed in the thermodynamically closed environment of a 506-l barometric calorimeter. Associated temperatures were calculated using a thermodynamic model informed by calculations with the Cheetah thermochemical code. Temperatures in the range of 2300-2800 K were calculated to persist for nearly the full 4 ms pressure observation time. After the detonation event, spores were characterized using optical microscopy and the number of viable spores was assessed. Results showed live spore survival rates in the range of 0.01%-1%. For the thermite tests, a similar, smaller-scale configuration was employed that examined the spore neutralization effects of two thermites: aluminum with iodine pentoxide and aluminum with potassium chlorate. Only the former mixture resulted in spore neutralization. These results indicate that the detonation environment produced by an explosive with no chemical biocides may provide effective spore neutralization similar to a deflagrating thermite containing iodine.

  7. Mirror Symmetry Breaking in Helical Polysilanes: Preference between Left and Right of Chemical and Physical Origin

    Directory of Open Access Journals (Sweden)

    Michiya Fujiki

    2010-08-01

    Full Text Available From elemental particles to human beings, matter is dissymmetric with respect to mirror symmetry. In 1860, Pasteur conjectured that biomolecular handedness— homochirality—may originate from certain inherent dissymmetric forces existing in the universe. Kipping, a pioneer of organosilicon chemistry, was interested in the handedness of sodium chlorate during his early research life. Since Kipping first synthesized several Si-Si bonded oligomers bearing phenyl groups, Si-Si bonded high polymers carrying various organic groups—polysilanes—can be prepared by sodium-mediated condensation of the corresponding organodichlorosilanes. Among these polysilanes, optically active helical polysilanes with enantiomeric pairs of organic side groups may be used for testing the mirror symmetry-breaking hypothesis by weak neutral current (WNC origin in the realm of chemistry and material science. Several theoretical studies have predicted that WNC-existing chiral molecules with stereogenic centers and/or stereogenic bonds allow for distinguishing between image and mirror image molecules. Based on several amplification mechanisms, theorists claimed that minute differences, though still very subtle, may be detectable by precise spectroscopic and physicochemical measurements if proper chiral molecular pairs were employed. The present paper reports comprehensively an inequality between six pairs of helical polysilane high polymers, presumably, detectable by (chiroptical and achiral 29Si-/13C- NMR spectra, and viscometric measurements.

  8. SYNTHESIS OF SULFUR-BASED WATER TREATMENT AGENT FROM SULFUR DIOXIDE WASTE STREAMS

    Energy Technology Data Exchange (ETDEWEB)

    Robert C. Brown; Maohong Fan

    2001-12-01

    We propose a process that uses sulfur dioxide from coal combustion as a raw material to synthesize polymeric ferric sulfate (PFS), a water treatment agent. The process uses sodium chlorate as an oxidant and ferrous sulfate as an absorbent. The major chemical mechanisms in this reaction system include oxidation, hydrolysis, and polymerization. Oxidation determines sulfur conversion efficiency while hydrolysis and polymerization control the quality of product. Many factors, including SO{sub 2} inlet concentration, flow rate of simulated flue gas, reaction temperature, addition rate of oxidant and stirring rate, may affect the efficiencies of SO{sub 2} removal. Currently, the effects of SO{sub 2} inlet concentration, the flow rate of simulated flue gas and addition rate of flue gas on removal efficiencies of SO{sub 2}, are being investigated. Experiments shown in this report have demonstrated that the conversion efficiencies of sulfur dioxide with ferrous sulfate as an absorbent are in the range of 60-80% under the adopted process conditions. However, the conversion efficiency of sulfur dioxide may be improved by optimizing reaction conditions to be investigated. Partial quality indices of the synthesized products, including Fe{sup 2+} concentration and total iron concentration, have been evaluated.

  9. Proton and deuterium NMR experiments in zero field. [Perdeuterated p-demethoxybenzene, perdeuterated malonic acid, diethyl terephthalate-d4, nonadecane-2,2'-D2, sodium propionate-D2

    Energy Technology Data Exchange (ETDEWEB)

    Millar, J.M.

    1986-02-01

    High field solid-state NMR lineshapes suffer from inhomogeneous broadening since resonance frequencies are a function of molecular orientation. Time domain zero field NMR is a two-dimensional field-cycling technique which removes this broadening by probing the evolution of the spin system under zero applied field. The simplest version, the sudden transition experiment, induces zero field evolution by the sudden removal of the applied magnetic field. Theory and experimental results of this experiment and several variations using pulsed dc magnetic fuelds to initiate zero field evolution are presented. In particular, the pulsed indirect detection method allows detection of the zero field spectrum of one nuclear spin species via another (usually protons) by utilizing the level crossings which occur upon adiabatic demagnetization to zero field. Experimental examples of proton/deuteron systems are presented which demonstrate the method results in enhanced sensitivity relative to that obtained in sudden transition experiments performed directly on deuterium. High resolution /sup 2/H NQR spectra of a series of benzoic acid derivatives are obtained using the sudden transition and indirect detection methods. Librational oscillations in the water molecules of barium chlorate monohydrate are studied using proton and deuterium ZF experiments. 177 refs., 88 figs., 2 tabs.

  10. Ammonia-oxidizing activity and microbial community structure in acid tea (Camellia sinensis) orchard soil

    Science.gov (United States)

    Okamura, K.; Takanashi, A.; Yamada, T.; Hiraishi, A.

    2012-03-01

    The purpose of this study was to determine the ammonia-oxidizing activity and the phylogentic composition of microorganisms involved in acid tea (Camellia sinensis) orchard soil. All soil samples were collected from three sites located in Tahara and Toyohashi, Aichi Prefecture, Japan. The potential nitrification rate (PNR) was measured by the chlorate inhibition method. The soil pH of tea orchards studied ranged from 2.78 to 4.84, differing significantly from sample to sample, whereas that of meadow and unplanted fields ranged from 5.78 to 6.35. The PNR ranged from 0.050 to 0.193 μg NO2--Ng-1 h-1 and were positively correlated with the soil pH (r2 = 0.382, pamoA genes. The detected archaeal clones separated from the cluster of the 'Soil clones' and tightly clustered with the clones originating from other acidic soil environments including the Chinese tea orchard soil. These results suggest that the specific archaeal populations dominate as the ammonia oxidizers in acid tea-orchard soils and possibly other acid soils, independent of geographic locations, which results from the adaptation to specific ecological niches.

  11. The use of ion chromatography in environmental and process control in the nuclear industry. Vol. 4

    International Nuclear Information System (INIS)

    Ion chromatography has become the method choice for determining sub ppb for inorganic anions and cations, such as chloride, sulfide, fluoride, sodium, potassium, and ammonium, in aqueous matrices. Steam generators in pressurized water reactors nuclear power plants occasionally experience tubing degradation by a variety of corrosion related mechanisms which depends on water chemistry. Ion chromatography is also used in other environmental applications such as air pollution, industrial hygiene, drinking water quality, and industrial waste treatment. In this paper, several methods of separation and detection are present and also a number of examples of samples for various types of water are shown. The examples will include sub ppb amounts of chloride, sulfate, sodium, potassium, and ammonium in high purity turbine steam. Testing of chlorinated drinking water for inorganic anions including chlorite, chloride chlorate nitrite, nitrate as other organic anions using chemically suppressed conductivity. The role of chemical suppression is discussed. The analysis of ppb levels of transition moles in high purity water using ion chromatography with post column derivatization and UV detection are reviewed. Testing of disinfected drinking water with ozone for bromate, the detection of cyanide in waste after acid digestion, and the detection of highly toxic hexavalent in the presence of trivalent chromium is discussed. A fast method for the analysis of rain water for anions and cations is described. The presentation will also show new method (chelation ion chromatography) which enables ppb levels of heavy metals to be determined as pollutants in difficult environmental matrices such seawater, and oyster tissue. 4 figs

  12. Determining the effects of routine fingermark detection techniques on the subsequent recovery and analysis of explosive residues on various substrates.

    Science.gov (United States)

    King, Sam; Benson, Sarah; Kelly, Tamsin; Lennard, Chris

    2013-12-10

    An offender who has recently handled bulk explosives would be expected to deposit latent fingermarks that are contaminated with explosive residues. However, fingermark detection techniques need to be applied in order for these fingermarks to be detected and recorded. Little information is available in terms of how routine fingermark detection methods impact on the subsequent recovery and analysis of any explosive residues that may be present. If an identifiable fingermark is obtained and that fingermark is found to be contaminated with a particular explosive then that may be crucial evidence in a criminal investigation (including acts of terrorism involving improvised explosive devices). The principal aims of this project were to investigate: (i) the typical quantities of explosive material deposited in fingermarks by someone who has recently handled bulk explosives; and (ii) the effects of routine fingermark detection methods on the subsequent recovery and analysis of explosive residues in such fingermarks. Four common substrates were studied: paper, glass, plastic (polyethylene plastic bags), and metal (aluminium foil). The target explosive compounds were 2,4,6-trinitrotoluene (TNT), pentaerythritol tetranitrate (PETN), and hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX), as well as chlorate and nitrate ions. Recommendations are provided in terms of the application of fingermark detection methods on surfaces that may contain explosive residues.

  13. (17)O NMR Investigation of Water Structure and Dynamics.

    Science.gov (United States)

    Keeler, Eric G; Michaelis, Vladimir K; Griffin, Robert G

    2016-08-18

    The structure and dynamics of the bound water in barium chlorate monohydrate were studied with (17)O nuclear magnetic resonance (NMR) spectroscopy in samples that are stationary and spinning at the magic-angle in magnetic fields ranging from 14.1 to 21.1 T. (17)O NMR parameters of the water were determined, and the effects of torsional oscillations of the water molecule on the (17)O quadrupolar coupling constant (CQ) were delineated with variable temperature MAS NMR. With decreasing temperature and reduction of the librational motion, we observe an increase in the experimentally measured CQ explaining the discrepancy between experiments and predictions from density functional theory. In addition, at low temperatures and in the absence of (1)H decoupling, we observe a well-resolved (1)H-(17)O dipole splitting in the spectra, which provides information on the structure of the H2O molecule. The splitting arises because of the homogeneous nature of the coupling between the two (1)H-(17)O dipoles and the (1)H-(1)H dipole. PMID:27454747

  14. Studying the processes of sulphates and chlorides extraction from water at low-waste water demineralization technology

    Directory of Open Access Journals (Sweden)

    Inna M. Тrus

    2014-12-01

    Full Text Available To solve the disposal problem of high-salinity liquid wastes resulting from the water demineralization, researched are the processes of chlorides’ and sulphates’ ion-exchange separation with further sulphates (in the form of calcium sulphate removal from the technological cycle. It is shown that the desulphatized water can be effectively desalinated by reverse osmosis filters, including low-pressure membranes Filmtec TW30-1812-50. The liquid waste obtained in form of concentrates, does contain chlorides, sodium ions and hardness ions. Established is that at these concentrates processing by lime and sodium carbonate or alkali and sodium carbonate they are softened with hardness decrease up to 0,25…0,95 mg-eq/dm3, which allows these solutions’ further electrolysis to obtain alkali and hydrochloric acid. Through direct electrolysis of concentrates, obtained by reverse osmosis water desalination at anionic membrane two-chamber electrolysers, we obtained a disinfectant solution containing chlorine oxigenates (active chlorine, hypochlorite, chlorite and sodium chlorate and duly effective in water sterilization. The resulting solution well keeps its properties and is promising for disinfection of natural and waste waters.

  15. 氯酸钾体系催化动力学光度法测定痕量钒(Ⅱ)%Catalytic kinetic spectrophotometric determination of trace vanadium

    Institute of Scientific and Technical Information of China (English)

    沈淑君; 邹小勇

    2012-01-01

    A new catalytic kinetic spectrophotometry was presented for the determination of trace vanadium ( V ).The catalytic effect was investigated for vanadium ( V ) on the oxidation of methyl red( C15H15N3O2 )by potassium chlorate ( KClO3 ) with ascorbic acid ( C6 Hg O6 ) as an activating agent in phosphoric acid solution (0.1 mol/L). The linear range is 0.09 ~ 7.0 ng/mL and the detection limit is 2.9 × 10 -2ng/mL. The proposed method has been successfully applied to the determination of vanadium ( V ) in water and food samples, and the satisfactory results were obtained.%研究了在0.1mol/LH3PO4介质中,活化剂抗坏血酸的作用下,V(Ⅴ)催化KClO3氧化甲基红褪色的指示反应,由此建立了一种测定痕量V(Ⅱ)的催化动力学光度新方法.研究了影响该催化褪色反应的因素.方法的线性范围为0.09~7.0ng/mL,检出限为2.9×10-2ng/mL.方法用于实际样品的测定.

  16. A stable room-temperature sodium-sulfur battery

    Science.gov (United States)

    Wei, Shuya; Xu, Shaomao; Agrawral, Akanksha; Choudhury, Snehashis; Lu, Yingying; Tu, Zhengyuan; Ma, Lin; Archer, Lynden A.

    2016-06-01

    High-energy rechargeable batteries based on earth-abundant materials are important for mobile and stationary storage technologies. Rechargeable sodium-sulfur batteries able to operate stably at room temperature are among the most sought-after platforms because such cells take advantage of a two-electron-redox process to achieve high storage capacity from inexpensive electrode materials. Here we report a room-temperature sodium-sulfur battery that uses a microporous carbon-sulfur composite cathode, and a liquid carbonate electrolyte containing the ionic liquid 1-methyl-3-propylimidazolium-chlorate tethered to SiO2 nanoparticles. We show that these cells can cycle stably at a rate of 0.5 C (1 C=1675, mAh g-1) with 600 mAh g-1 reversible capacity and nearly 100% Coulombic efficiency. By means of spectroscopic and electrochemical analysis, we find that the particles form a sodium-ion conductive film on the anode, which stabilizes deposition of sodium. We also find that sulfur remains interred in the carbon pores and undergo solid-state electrochemical reactions with sodium ions.

  17. Water-Quality Constituents, Dissolved-Organic-Carbon Fractions, and Disinfection By-Product Formation in Water from Community Water-Supply Wells in New Jersey, 1998-99

    Science.gov (United States)

    Hopple, Jessica A.; Barringer, Julia L.; Koleis, Janece

    2007-01-01

    to a pH of 7, dosed with sodium hypochlorite, and incubated for 168 hours (seven days) at 25 ?C to form disinfection by-products (DBPs). Concentrations of the DBPs-trihalomethanes, haloacetic acids, haloacetonitriles, and chlorate-were measured. Concentrations of these compounds, with few exceptions, were higher in water from Coastal Plain wells than from wells in glacial and bedrock aquifers. The organic-carbon fractions were dosed with sodium hypochlorite, incubated for 168 hours at 25 ?C, and analyzed for trihalomethanes, haloacetic acids, haloacetonitriles, and chlorate. Concentrations of trihalomethanes and haloacetic acids were higher in most of the hydrophobic organic-acid fractions than in the hydrophilic fractions, with the highest concentrations in samples from Coastal Plain aquifers. Traces of haloacetonitriles were measured, mostly in the hydrophilic fraction. The aromaticity of the precursor DOC, as estimated by measurements of the absorbance of ultraviolet light at 254 nanometers, apparently is a factor in the DBP formation potentials determined, as aromaticity was greater in the samples that developed high concentrations of DBPs. VOCs may have contributed to the organic carbon present in some of the samples, but much of the DOC present in water from the 20 wells appeared to be natural in origin. The sediments of the Coastal Plain aquifers, in particular, contain substantial amounts of organic matter, which contribute ammonia, organic nitrogen, and aromatic DOC compounds to the ground water. Thus, the geologic characteristics of the aquifers appear to be a major factor in the potential for ground water to form DBPs when chlorinated.

  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. 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

  20. "Let's take back our roots through Science". The Sicilian Sulfur: a mineralogical treasure to rediscover.

    Science.gov (United States)

    Parisi, Bianca

    2015-04-01

    The name of sulfur is synonymous of Sicily! Sicilian Sulfur minerals and evaporitic deposits are well-known because they are connected with an important evolution stage of the old mediterranean area. In this Island, in the southern part of Italy, a geological formation of Messinian age, called "gessoso solfifera", outcrops. These rocks are widespread in the south and south-west Sicily, and, there, salt mines and "zolfare", sulfur mines, were located. The formation is characterized by large amounts of gypsum, potassium salts, sodium chlorates and other deposits. Most of the main mineralogical museum collections all over the world have at least a sample of one of these minerals that are usually characterized by a high aesthetic quality. When I proposed a lesson on the origin of sulfur in evaporitic rocks, I realized that an important part of the hystory of our region was in danger to be forgotten by younger generation. The exploitation of this mineral resource in the past is strictly linked to the troubled social and cultural transformation of Sicily during the last century. Thus, this is a particularly suitable topic for a multidisciplinary approach. In cooperation with the Mineralogical Museum (SteBiCeF Department, University of Palermo), a learning project was proposed to a group of 4th year high school students. It has been carrying on in order to develop the knowledge of the geological and chemical features of evaporitic deposits and to promote scientific abilities together with a better understanding of social-environmental issues. Project aims and activities include: ➢ Solubility and saturation experiments to reconstruct a simplified model of minerals deposition ➢ Working in groups: collection of data about old geological outcrops and current evaporating basins where rocks are forming in the world as well as information on sicilian mines from literature and historical documents (video, interviews, pictures, newspapers and others) ➢ a guided tour of the

  1. Role of phosphate and other proton-donating anions in respiration-coupled transport of Ca2+ by mitochondria.

    Science.gov (United States)

    Lehninger, A L

    1974-04-01

    Measurements of extra oxygen consumption, (45)Ca(2+) uptake, and the osmotic expansion of the matrix compartment show that not all permeant anions are capable of supporting and accompanying the energy-dependent transport of Ca(2+) from the medium into the matrix in respiring rat-liver mitochondria. Phosphate, arsenate, acetate, butyrate, beta-hydroxybutyrate, lactate, and bicarbonate + CO(2) supported Ca(2+) uptake, whereas the permeant anions, nitrate, thiocyanate, chlorate, and perchlorate, did not. The active anions share a common denominator, the potential ability to donate a proton to the mitochondrial matrix; the inactive anions lack this capacity. Phosphate and the other active permeant anions move into the matrix in response to the alkaline-inside electrochemical gradient of protons generated across the mitochondrial membrane by electron transport, thus forming a negative-inside anion gradient. It is postulated that the latter gradient is the immediate "pulling" force for the influx of Ca(2+) on the electrogenic Ca(2+) carrier in respiring mitochondria under intracellular conditions. Since mitochondria in the cell are normally exposed to an excess of phosphate (and the bicarbonate-CO(2) system), particularly in state 4, inward transport of these proton-yielding anions probably precedes and is necessary for inward transport of Ca(2+) and other cations under biological conditions. These observations indicate that a negative-inside gradient of phosphate generated by electron transport is a common step and provides the immediate motive power not only for (a) the inward transport of dicarboxylates and tricarboxylates and (b) the energy-dependent exchange of external ADP(3-) for internal ATP(4-) during oxidative phosphorylation, as has already been established, but also for (c) the inward transport of Ca(2+), K(+), and other cations.

  2. Application of electrochemical advanced oxidation processes to the mineralization of the herbicide diuron.

    Science.gov (United States)

    Pipi, Angelo R F; Sirés, Ignasi; De Andrade, Adalgisa R; Brillas, Enric

    2014-08-01

    Here, solutions with 0.185mM of the herbicide diuron of pH 3.0 have been treated by electrochemical advanced oxidation processes (EAOPs) like electrochemical oxidation with electrogenerated H2O2 (EO-H2O2), electro-Fenton (EF) and UVA photoelectro-Fenton (PEF) or solar PEF (SPEF). Trials were performed in stirred tank reactors of 100mL and in a recirculation flow plant of 2.5L using a filter-press reactor with a Pt or boron-doped diamond (BDD) anode and an air-diffusion cathode for H2O2 electrogeneration. Oxidant hydroxyl radicals were formed from water oxidation at the anode and/or in the bulk from Fenton's reaction between added Fe(2+) and generated H2O2. In both systems, the relative oxidation ability of the EAOPs increased in the sequence EO-H2O2treatment with BDD was the most potent method, yielding 93% mineralization after 360 min at 100 mA cm(-2). In the flow plant, the SPEF process attained a maximum mineralization of 70% at 100 mA cm(-2). Lower current densities slightly reduced the mineralization degree in SPEF, enhancing the current efficiency and dropping the energy consumption. The diuron decay always obeyed a pseudo-first-order kinetics, with a much greater apparent rate constant in EF and SPEF compared to EO-H2O2. Oxalic and oxamic acids were detected as final carboxylic acids. Ammonium and chloride ions were also released, the latter ion being partially converted into chlorate and perchlorate ions at the BDD surface.

  3. Silicic volcanism on Mars evidenced by tridymite in high-SiO2 sedimentary rock at Gale crater

    Science.gov (United States)

    Morris, Richard V.; Vaniman, David T.; Blake, David F.; Gellert, Ralf; Chipera, Steve J.; Rampe, Elizabeth B.; Ming, Douglas W.; Morrison, Shaunna M.; Downs, Robert T.; Treiman, Allan H.; Yen, Albert S.; Grotzinger, John P.; Achilles, Cherie N.; Bristow, Thomas F.; Crisp, Joy A.; Des Marais, David J.; Farmer, Jack D.; Fendrich, Kim V.; Frydenvang, Jens; Graff, Trevor G.; Morookian, John-Michael; Stolper, Edward M.; Schwenzer, Susanne P.

    2016-06-01

    Tridymite, a low-pressure, high-temperature (>870 °C) SiO2 polymorph, was detected in a drill sample of laminated mudstone (Buckskin) at Marias Pass in Gale crater, Mars, by the Chemistry and Mineralogy X-ray diffraction instrument onboard the Mars Science Laboratory rover Curiosity. The tridymitic mudstone has ˜40 wt.% crystalline and ˜60 wt.% X-ray amorphous material and a bulk composition with ˜74 wt.% SiO2 (Alpha Particle X-Ray Spectrometer analysis). Plagioclase (˜17 wt.% of bulk sample), tridymite (˜14 wt.%), sanidine (˜3 wt.%), cation-deficient magnetite (˜3 wt.%), cristobalite (˜2 wt.%), and anhydrite (˜1 wt.%) are the mudstone crystalline minerals. Amorphous material is silica-rich (˜39 wt.% opal-A and/or high-SiO2 glass and opal-CT), volatile-bearing (16 wt.% mixed cation sulfates, phosphates, and chlorides‑perchlorates‑chlorates), and has minor TiO2 and Fe2O3T oxides (˜5 wt.%). Rietveld refinement yielded a monoclinic structural model for a well-crystalline tridymite, consistent with high formation temperatures. Terrestrial tridymite is commonly associated with silicic volcanism, and detritus from such volcanism in a “Lake Gale” catchment environment can account for Buckskin's tridymite, cristobalite, feldspar, and any residual high-SiO2 glass. These cogenetic detrital phases are possibly sourced from the Gale crater wall/rim/central peak. Opaline silica could form during diagenesis from high-SiO2 glass, as amorphous precipitated silica, or as a residue of acidic leaching in the sediment source region or at Marias Pass. The amorphous mixed-cation salts and oxides and possibly the crystalline magnetite (otherwise detrital) are primary precipitates and/or their diagenesis products derived from multiple infiltrations of aqueous solutions having variable compositions, temperatures, and acidities. Anhydrite is post lithification fracture/vein fill.

  4. Acute exposure to the biopesticide azadirachtin affects parameters in the gills of common carp (Cyprinus carpio).

    Science.gov (United States)

    Murussi, Camila R; Costa, Maiara D; Leitemperger, Jossiele W; Flores-Lopes, Fábio; Menezes, Charlene C; Loebens, Luisa; de Avila, Luis Antonio; Rizzetti, Tiele M; Adaime, Martha B; Zanella, Renato; Loro, Vania L

    2016-02-01

    The biopesticide, azadirachtin (Aza) is less hazardous to the environment, but may cause several toxic effects in aquatic organisms. The Cyprinus carpio (n=12, for all concentrations) after 10days of acclimation under controlled conditions, were exposed at 20, 40, and 60μL/L of Aza during 96h. After this period, fish were anesthetized and euthanized then mucus layer and gills collected. In this study, the effects of exposure to different Aza concentrations were analysed through a set of biomarkers: Na(+)/K(+-)ATPase, lipid peroxidation (TBARS), protein carbonyl (PC), superoxide dismutase (SOD), glutathione-S-transferase (GST), catalase (CAT), glutathione peroxidase (GPx), non-protein thiols (NPSH), ascorbic acid (AsA) and histological parameters and, yet, protein and glucose concentration in the surface area of mucous layer. Na(+)K(+-)ATPase was inhibited at 40 and 60μL/L compared to control. TBARS decreased at 40μL/L compared to control. PC, SOD and GST increased at 60μL/L in comparison to control. CAT increased at 20 and 60μL/L, and GPx increased in all Aza concentrations compared to control. NPSH decreased and AsA increased in all concentrations in comparison to control. Histological analyses demonstrated an increase in the intensity of the damage with increasing Aza concentration. Alterations in histological examination were elevation and hypertrophy of the epithelial cells of the secondary filament, hypertrophy and hyperplasia of the mucous and chlorate cells and lamellar aneurism. Glucose and protein concentrations in mucus layer increased at 60μL/L compared to control. In general, we suggest that 60μL/L Aza concentration affected several parameters causing disruptions carp metabolism. PMID:26689640

  5. Silicic volcanism on Mars evidenced by tridymite in high-SiO2 sedimentary rock at Gale crater.

    Science.gov (United States)

    Morris, Richard V; Vaniman, David T; Blake, David F; Gellert, Ralf; Chipera, Steve J; Rampe, Elizabeth B; Ming, Douglas W; Morrison, Shaunna M; Downs, Robert T; Treiman, Allan H; Yen, Albert S; Grotzinger, John P; Achilles, Cherie N; Bristow, Thomas F; Crisp, Joy A; Des Marais, David J; Farmer, Jack D; Fendrich, Kim V; Frydenvang, Jens; Graff, Trevor G; Morookian, John-Michael; Stolper, Edward M; Schwenzer, Susanne P

    2016-06-28

    Tridymite, a low-pressure, high-temperature (>870 °C) SiO2 polymorph, was detected in a drill sample of laminated mudstone (Buckskin) at Marias Pass in Gale crater, Mars, by the Chemistry and Mineralogy X-ray diffraction instrument onboard the Mars Science Laboratory rover Curiosity The tridymitic mudstone has ∼40 wt.% crystalline and ∼60 wt.% X-ray amorphous material and a bulk composition with ∼74 wt.% SiO2 (Alpha Particle X-Ray Spectrometer analysis). Plagioclase (∼17 wt.% of bulk sample), tridymite (∼14 wt.%), sanidine (∼3 wt.%), cation-deficient magnetite (∼3 wt.%), cristobalite (∼2 wt.%), and anhydrite (∼1 wt.%) are the mudstone crystalline minerals. Amorphous material is silica-rich (∼39 wt.% opal-A and/or high-SiO2 glass and opal-CT), volatile-bearing (16 wt.% mixed cation sulfates, phosphates, and chlorides-perchlorates-chlorates), and has minor TiO2 and Fe2O3T oxides (∼5 wt.%). Rietveld refinement yielded a monoclinic structural model for a well-crystalline tridymite, consistent with high formation temperatures. Terrestrial tridymite is commonly associated with silicic volcanism, and detritus from such volcanism in a "Lake Gale" catchment environment can account for Buckskin's tridymite, cristobalite, feldspar, and any residual high-SiO2 glass. These cogenetic detrital phases are possibly sourced from the Gale crater wall/rim/central peak. Opaline silica could form during diagenesis from high-SiO2 glass, as amorphous precipitated silica, or as a residue of acidic leaching in the sediment source region or at Marias Pass. The amorphous mixed-cation salts and oxides and possibly the crystalline magnetite (otherwise detrital) are primary precipitates and/or their diagenesis products derived from multiple infiltrations of aqueous solutions having variable compositions, temperatures, and acidities. Anhydrite is post lithification fracture/vein fill.

  6. Removal of organic contaminants from secondary effluent by anodic oxidation with a boron-doped diamond anode as tertiary treatment

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Segura, Sergi, E-mail: sergigarcia@ub.edu [Advanced Water Management Centre, The University of Queensland, Level 4, Gehrmann Bld. (60), St Lucia, QLD 072 (Australia); Laboratori d’Electroquímica dels Materials i del Medi Ambient, Departament de Química Física, Facultat de Química, Universitat de Barcelona, Martí i Franquès 1-11, 08028 Barcelona (Spain); Keller, Jürg [Advanced Water Management Centre, The University of Queensland, Level 4, Gehrmann Bld. (60), St Lucia, QLD 072 (Australia); Brillas, Enric [Laboratori d’Electroquímica dels Materials i del Medi Ambient, Departament de Química Física, Facultat de Química, Universitat de Barcelona, Martí i Franquès 1-11, 08028 Barcelona (Spain); Radjenovic, Jelena, E-mail: j.radjenovic@awmc.uq.edu.au [Advanced Water Management Centre, The University of Queensland, Level 4, Gehrmann Bld. (60), St Lucia, QLD 072 (Australia)

    2015-02-11

    Graphical abstract: - Highlights: • Mineralization of secondary effluent by anodic oxidation with BDD anode. • Complete removal of 29 pharmaceuticals and pesticides at trace level concentrations. • Organochlorine and organobromine byproducts were formed at low μM concentrations. • Chlorine species evolution assessed to evaluate the anodic oxidation applicability. - Abstract: Electrochemical advanced oxidation processes (EAOPs) have been widely investigated as promising technologies to remove trace organic contaminants from water, but have rarely been used for the treatment of real waste streams. Anodic oxidation with a boron-doped diamond (BDD) anode was applied for the treatment of secondary effluent from a municipal sewage treatment plant containing 29 target pharmaceuticals and pesticides. The effectiveness of the treatment was assessed from the contaminants decay, dissolved organic carbon and chemical oxygen demand removal. The effect of applied current and pH was evaluated. Almost complete mineralization of effluent organic matter and trace contaminants can be obtained by this EAOP primarily due to the action of hydroxyl radicals formed at the BDD surface. The oxidation of Cl{sup −} ions present in the wastewater at the BDD anode gave rise to active chlorine species (Cl{sub 2}/HClO/ClO{sup −}), which are competitive oxidizing agents yielding chloramines and organohalogen byproducts, quantified as adsorbable organic halogen. However, further anodic oxidation of HClO/ClO{sup −} species led to the production of ClO{sub 3}{sup −} and ClO{sub 4}{sup −} ions. The formation of these species hampers the application as a single-stage tertiary treatment, but posterior cathodic reduction of chlorate and perchlorate species may reduce the risks associated to their presence in the environment.

  7. Ozone enhanced activity of aqueous titanium dioxide suspensions for photodegradation of 4-chloronitrobenzene

    International Nuclear Information System (INIS)

    The TiO2/UV/O3 process has been employed to remove 4-chloronitrobenzene (4-CNB) and compared to UV/air, O3, TiO2/O3, TiO2/UV/O2 and UV/O3 five parallel oxidation pathways. The reaction activities of these six processes were tested in aqueous using electron paramagnetic resonance (EPR) spin trapping technique with 5,5-dimethyl-1-pyrroline N-oxide (DMPO) spin trap. Moreover, the effects of ozone dosage, catalyst dosage and initial solution pH on the degradation of 4-CNB by TiO2/UV/O3 process were also investigated. Results showed that the TiO2/UV/O3 is the most efficient process for complete mineralization of 4-CNB since the combination of photocatalytic oxidation with ozone has a synergistic effect. The relative intensity of DMPO-·OH follows the order of UV/air 3 2/O3 3 2/UV/O2 2/UV/O3. In TiO2/UV/O3 process, the ozone and catalyst dosage are found to have a significant impact on the process efficiency whereas initial pH has relatively less effect. Chlorine atoms of 4-CNB are absolutely oxidized to chloride anions when the ozone dosage in the range of 5-18 mg/min, or the catalyst dosage ranging from 1.0 to 2.0 g/L. Part of chloride anions would be further oxidized to chlorate(V) ions if the ozone dosage exceeds 24 mg/min, or the catalyst dosage exceeds 2.0 g/L.

  8. 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.

  9. Photochemical oxidation of chloride ion by ozone in acid aqueous solution.

    Science.gov (United States)

    Levanov, Alexander V; Isaykina, Oksana Ya; Amirova, Nazrin K; Antipenko, Ewald E; Lunin, Valerii V

    2015-11-01

    The experimental investigation of chloride ion oxidation under the action of ozone and ultraviolet radiation with wavelength 254 nm in the bulk of acid aqueous solution at pH 0-2 has been performed. Processes of chloride oxidation in these conditions are the same as the chemical reactions in the system O3 - OH - Cl(-)(aq). Despite its importance in the environment and for ozone-based water treatment, this reaction system has not been previously investigated in the bulk solution. The end products are chlorate ion ClO3(-) and molecular chlorine Cl2. The ions of trivalent iron have been shown to be catalysts of Cl(-) oxidation. The dependencies of the products formation rates on the concentrations of O3 and H(+) have been studied. The chemical mechanism of Cl(-) oxidation and Cl2 emission and ClO3(-) formation has been proposed. According to the mechanism, the dominant primary process of chloride oxidation represents the complex interaction with hydroxyl radical OH with the formation of Cl2(-) anion-radical intermediate. OH radical is generated on ozone photolysis in aqueous solution. The key subsequent processes are the reactions Cl2(-) + O3 → ClO + O2 + Cl(-) and ClO + H2O2 → HOCl + HO2. Until the present time, they have not been taken into consideration on mechanistic description and modelling of Cl(-) oxidation. The final products are formed via the reactions 2ClO → Cl2O2, Cl2O2 + H2O → 2H(+) + Cl(-) + ClO3(-) and HOCl + H(+) + Cl(-) ⇄ H2O + Cl2. Some portion of chloride is oxidized directly by O3 molecule with the formation of molecular chlorine in the end.

  10. Perchlorate and volatiles of the brine of Lake Vida (Antarctica): Implication for the in situ analysis of Mars sediments

    Science.gov (United States)

    Kenig, Fabien; Chou, Luoth; McKay, Christopher P.; Jackson, W. Andrew; Doran, Peter T.; Murray, Alison E.; Fritsen, Christian H.

    2016-07-01

    The cold (-13.4°C), cryoencapsulated, anoxic, interstitial brine of the >27 m thick ice of Lake Vida (Victoria Valley, Antarctica) contains 49 µg · L-1 of perchlorate and 11 µg · L-1 of chlorate. Lake Vida brine (LVBr) may provide an analog for potential oxychlorine-rich subsurface brine on Mars. LVBr volatiles were analyzed by solid-phase microextraction (SPME) gas chromatography-mass spectrometry (GC-MS) with two different SPME fibers. With the exception of volatile organic sulfur compounds, most other volatiles observed were artifacts produced in the GC injector when the thermal decomposition products of oxychlorines reacted with reduced carbon derived from LVBr and the SPME fiber phases. Analysis of MilliQ water with perchlorate (40 µg · L-1) showed low level of organic artifacts, reflecting carbon limitation. In order to observe sample-derived organic compounds, both in analog samples and on Mars, the molar abundance of reduced carbon in a sample must exceed those of O2 and Cl2 produced during decomposition of oxychlorines. This suggests that the abundance of compounds observed by the Sample Analysis at Mars (SAM) instruments in Sheepbed samples (CB-3, CB5, and CB6) may be controlled by an increase in the reduced-carbon/oxychlorine ratio of these samples. To increase chances of in situ detection of Martian organics during pyrolysis-GC-MS, we propose that the derivatization agents stored on SAM may be used as an external source of reduced carbon, increasing artificially the reduced-carbon to perchlorate ratio during pyrolysis, allowing the expression of more abundant and perhaps more diverse Martian organic matter.

  11. Methane oxidation linked to chlorite dismutation

    Science.gov (United States)

    Miller, Laurence G.; Baesman, Shaun M.; Carlström, Charlotte I.; Coates, John D.; Oremland, Ronald S.

    2014-01-01

    We examined the potential for CH4 oxidation to be coupled with oxygen derived from the dissimilatory reduction of perchlorate, chlorate, or via chlorite (ClO−2) dismutation. Although dissimilatory reduction of ClO−4 and ClO−3 could be inferred from the accumulation of chloride ions either in spent media or in soil slurries prepared from exposed freshwater lake sediment, neither of these oxyanions evoked methane oxidation when added to either anaerobic mixed cultures or soil enriched in methanotrophs. In contrast, ClO−2 amendment elicited such activity. Methane (0.2 kPa) was completely removed within several days from the headspace of cell suspensions of Dechloromonas agitata CKB incubated with either Methylococcus capsulatus Bath or Methylomicrobium album BG8 in the presence of 5 mM ClO−2. We also observed complete removal of 0.2 kPa CH4 in bottles containing soil enriched in methanotrophs when co-incubated with D. agitata CKB and 10 mM ClO−2. However, to be effective these experiments required physical separation of soil from D. agitata CKB to allow for the partitioning of O2 liberated from chlorite dismutation into the shared headspace. Although a link between ClO−2 and CH4 consumption was established in soils and cultures, no upstream connection with either ClO−4 or ClO−3 was discerned. This result suggests that the release of O2 during enzymatic perchlorate reduction was negligible, and that the oxygen produced was unavailable to the aerobic methanotrophs.

  12. Sweet and Sour: Attenuating Sulfidogenesis in an Advective Flow Column System with Perchlorate or Nitrate Treatment

    Science.gov (United States)

    Engelbrektson, A. L.; Hubbard, C. G.; Piceno, Y.; Boussina, A.; Jin, Y.; Dubinsky, E. A.; Tom, L.; Hu, P.; Conrad, M. E.; Anderson, G. L.; Coates, J. D.

    2013-12-01

    Hydrogen sulfide (H2S) biogenesis in oil reservoirs is a primary cause of souring and of associated costs in reservoir and pipeline maintenance. In addition to the corrosive effects of the H2S itself, abiotic and biological oxidation also generates sulfuric acid, further degrading metallic surfaces. Amending these environments with perchlorate (ClO4-) resolves these problems by inhibition of biological sulfate reduction and re-oxidation of H2S to elemental sulfur by dissimilatory (per)chlorate reducing bacteria (DPRB). Triplicate flow through columns packed with San Francisco bay sediment were flushed with bay water ([SO4=] = 25-30 mM) containing yeast extract with 50 mM inhibitor concentrations (NO3-or ClO4-) decreasing to 25 mM and finally 12.5 mM. Influent and effluent geochemistry was monitored and DNA was prepared from the sediment bed for microbial community analysis. Souring was reversed by both treatments (at 50 mM) compared to the control columns that had no ion addition. Nitrate began to re-sour when treatment concentration was decreased to 25 mM but treatment had to be decreased to 12.5 mM before the perchlorate treated columns began to re-sour. However, the treated columns re-soured to a lesser extent than the control columns. Phylochip microbial community analyses indicated microbial community shifts and phylogenetic clustering by treatment. Isotopic analysis of sulfate showed trends that broadly agreed with the geochemistry but also suggested further sulfur cycling was occurring. This study indicates that perchlorate shows great promise as an inhibitor of sulfidogenesis in natural communities and provides insight into which organisms are involved in this process.

  13. Characterization of a hybrid-smectite nanomaterial formed by immobilizing of N-pyridin-2-ylmethylsuccinamic acid onto (3-aminopropyl)triethoxysilane modified smectite and its potentiometric sensor application

    Science.gov (United States)

    Topcu, Cihan; Caglar, Sema; Caglar, Bulent; Coldur, Fatih; Cubuk, Osman; Sarp, Gokhan; Gedik, Kubra; Bozkurt Cirak, Burcu; Tabak, Ahmet

    2016-09-01

    A novel N-pyridin-2-ylmethylsuccinamic acid-functionalized smectite nanomaterial was synthesized by immobilizing of N-pyridin-2-ylmethylsuccinamic acid through chemical bonding onto (3-aminopropyl)triethoxysilane modified smectite. The structural, thermal, morphological and surface properties of raw, silane-grafted and the N-pyridin-2-ylmethylsuccinamic acid-functionalized smectites were investigated by various characterization techniques. The thermal analysis data showed the presence of peaks in the temperature range from 200 °C to 600 °C due to the presence of physically adsorbed silanes, intercalated silanes, surface grafted silanes and chemically grafted silane molecules between the smectite layers. The powder x-ray diffraction patterns clearly indicated that the aminopropyl molecules also intercalated into the smectite interlayers as bilayer arrangement whereas N-pyridin-2-ylmethylsuccinamic acid molecules were only attached to 3-aminopropyltriethoxysilane molecules on the external surface and edges of clay and they did not intercalate. Fourier transform infrared spectroscopy confirms N-pyridin-2-ylmethylsuccinamic acid molecules bonding through the amide bond between the amine group of aminopropyltriethoxysilane molecules and a carboxylic acid functional group of N-pyridin-2-ylmethylsuccinamic acid molecules. The guest molecules functionalized onto the smectite caused significant alterations in the textural and morphological parameters of the raw smectite. The anchoring of N-pyridin-2-ylmethylsuccinamic acid molecules led to positive electrophoretic mobility values when compared to starting materials. N-pyridin-2-ylmethylsuccinamic acid-functionalized smectite was employed as an electroactive ingredient in the structure of potentiometric PVC-membrane sensor. The sensor exhibited more selective potentiometric response towards chlorate ions compared to the other common anionic species.

  14. Optimizing potentiometric ionophore and electrode design for environmental on-site control of antibiotic drugs: application to sulfamethoxazole.

    Science.gov (United States)

    Almeida, S A A; Truta, Liliana A A N A; Queirós, Raquel B; Montenegro, M C B S M; Cunha, Alexandre L; Sales, M G F

    2012-05-15

    Potentiometric sensors are typically unable to carry out on-site monitoring of environmental drug contaminants because of their high limits of detection (LODs). Designing a novel ligand material for the target analyte and managing the composition of the internal reference solution have been the strategies employed here to produce for the first time a potentiometric-based direct reading method for an environmental drug contaminant. This concept has been applied to sulfamethoxazole (SMX), one of the many antibiotics used in aquaculture practices that may occur in environmental waters. The novel ligand has been produced by imprinting SMX on the surface of graphitic carbon nanostructures (CN)environmental water. The best membrane cocktail was applied on the smaller end of a 1000 μL micropipette tip made of polypropylene. The tip was then filled with inner reference solution containing SMX and chlorate (as interfering compound). The corresponding concentrations were studied for 1 × 10(-5) to 1 × 10(-10) and 1 × 10(-3) to 1 × 10(-8)mol/L. The best condition allowed the detection of 5.92 ng/L (or 2.3 × 10(-8)mol/L) SMX for a sub-Nernstian slope of -40.3 mV/decade from 5.0 × 10(-8) to 2.4 × 10(-5)mol/L. The described sensors were found promising devices for field applications. The good selectivity of the sensory materials together with a carefully selected composition for the inner reference solution allowed LODs near the nanomolar range. Both solid-contact and "pipette tip"-based sensors were successfully applied to the analysis of aquaculture waters.

  15. Emprêgo de desfolhantes na cultura da batatinha The use of potato vine killers

    Directory of Open Access Journals (Sweden)

    O. J. Boock

    1962-01-01

    Full Text Available Uma das medidas que se impõem para a melhoria do estado de sanidade dos tubérculos de batatinha (Solanum tuberosum L., tanto para o consumo como principalmente para o plantio, é a destruição da folhagem com alguma antecedência à colheita normal Além dessa melhoria, tal prática permite colocar o produto no mercado antes das épocas das maiores safras obtendo-se maiores lucros. Neste trabalho são apresentados resultados obtidos com o emprêgo de desfolhantes físicos, químicos e mecânicos, para determinação dos mais eficientes nas condições locais. Tal prática, em relação ao estado de sanidade, principalmente quanto às moléstias de vírus e apodrecimentos devidos à requeima (Phytophthora infestans e pinta preta (Alternaria solani, será objeto de novos experimentos, utilizando-se como desfolhante aquêles que, neste trabalho, se mostraram mais eficientes e econômicos, como foi o casododinitro-orto-secundário-butil-fenol e do dínitro-cresol.This paper discusses the results of preliminary tests for determining the best way to kill the potato vine under the conditions of the State of São Paulo. Of the methods compared (cutting or flaming the vines, or spraying them with sodium chlorate, sodium arsenite, dinitro cresol or dinitro-o-sec-butyl phenol, spraying with the dinitro derivatives seemed to be the best. Further experiments are needed to observe the incidence of virus diseases and rots caused by Phytophthora infstans and Alternaria solani in the seed potatoes coming from fields treated with the latter products.

  16. Adsorption of arsenate and arsenite from aqueous solutions by cerium-loaded cation exchange resin

    Institute of Scientific and Technical Information of China (English)

    HE Zongliang; TIAN Senlin; NING Ping

    2012-01-01

    The removal of arsenic from water and wastewater is obligatory.Resin is one of the most effective adsorbents for the removal of arsenic.In order to improve the adsorption capacity of resin,a new cerium-loaded cation exchange resin arsenic adsorbent was prepared by impregnating cerium into the cation exchange resin.Batch adsorption experiments under various conditions,such as time,temperature,pH and with coexisting ions were carried out to evaluate the adsorption characteristics of cerium-loaded resin in the removal of As(Ⅴ) and As(Ⅲ) from aqueous solutions.The results showed that the adsorption kinetics of As(Ⅴ) and As(Ⅲ) obeyed a pseudo second-order kinetic model and the adsorption rate constants were 0.3159 and 0.5215 g·mg-1·min-1,respectively.The adsorption of As(Ⅴ) followed the Freundlich adsorption isotherm model and the adsorption isotherm data for As(Ⅲ) fitted well to the Langmuir equation model.The adsorption capacities were 1.0278 mg/g for As(Ⅴ) and 2.5297 mg/g for As(Ⅲ).Both the adsorption of As(Ⅴ) and As(Ⅲ) were found to be pH sensitive and the optimum pH was found to be 5-6.Except for the phosphate ion,the coexisting anionics,such as nitrate,chlorate,sulphate and carbonate,showed no remarkable effect on AS(Ⅴ) and As(Ⅲ) adsorption.The desorption and regeneration study showed that the adsorption capacity of Ce-loaded resin for As(Ⅴ) and As(Ⅲ) could be restored to 97.80% and 69.61%,respectively,using 0.5 mol/L sodium hydroxide solution.

  17. Chlorine and Sulfur Volatiles from in Situ Measurements of Martian Surface Materials

    Science.gov (United States)

    Clark, B. C.

    2014-12-01

    A sentinel discovery by the first in situ measurements on Mars was the high sulfur and chlorine content of global-wide soils. A variety of circumstantial evidence led to the conclusion that soil S is in the form of sulfate, and the Cl is probably chloride. An early hypothesis states that these volatiles are emitted as gases from magmas, and quickly react with dust, soil, and exposed rocks. Subsequent determination that SNC meteorites are also samples of the martian crust revealed a significantly higher S content, as sulfide, than terrestrial igneous rocks but substantially less than in soils. The ensuing wet chemical analyses by the high-latitude Phoenix mission discovered not only chloride but also perchlorate and possibly chlorate. MSL data now also implicate perchlorate at low latitudes. Gaseous interactions may have produced amorphous material on grain surfaces without forming stoichiometric salts. Yet, when exposed to liquid water, Phoenix samples released electrolytes, indicating that the soils have not been leached by rain or fresh groundwater. Sulfate occurrences at many locations on Mars, as well as some chloride enrichments, have now been discovered by remote sensing, Landed missions have discovered Cl-enrichments and ferric, Mg, Ca and more complex sulfates as duricrust, subsurface soil horizons, sandstone evaporites, and rock coatings - most of which cannot be detected from orbit. Salt-forming volatiles affect habitability wherever they are in physical contact: physicochemical parameters (ionic strength, freezing point, water activity); S is an essential element for terrestrial organisms; perchlorate is an oxidant which can degrade some organics but also can be utilized as an energy source; the entire valence range of S-compounds has been exploited by diverse microbiota on Earth. Whether such salt-induced conditions are "extremes" of habitability depends on the relative abundance of liquid H2O.

  18. Removal of organic contaminants from secondary effluent by anodic oxidation with a boron-doped diamond anode as tertiary treatment

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • Mineralization of secondary effluent by anodic oxidation with BDD anode. • Complete removal of 29 pharmaceuticals and pesticides at trace level concentrations. • Organochlorine and organobromine byproducts were formed at low μM concentrations. • Chlorine species evolution assessed to evaluate the anodic oxidation applicability. - Abstract: Electrochemical advanced oxidation processes (EAOPs) have been widely investigated as promising technologies to remove trace organic contaminants from water, but have rarely been used for the treatment of real waste streams. Anodic oxidation with a boron-doped diamond (BDD) anode was applied for the treatment of secondary effluent from a municipal sewage treatment plant containing 29 target pharmaceuticals and pesticides. The effectiveness of the treatment was assessed from the contaminants decay, dissolved organic carbon and chemical oxygen demand removal. The effect of applied current and pH was evaluated. Almost complete mineralization of effluent organic matter and trace contaminants can be obtained by this EAOP primarily due to the action of hydroxyl radicals formed at the BDD surface. The oxidation of Cl− ions present in the wastewater at the BDD anode gave rise to active chlorine species (Cl2/HClO/ClO−), which are competitive oxidizing agents yielding chloramines and organohalogen byproducts, quantified as adsorbable organic halogen. However, further anodic oxidation of HClO/ClO− species led to the production of ClO3− and ClO4− ions. The formation of these species hampers the application as a single-stage tertiary treatment, but posterior cathodic reduction of chlorate and perchlorate species may reduce the risks associated to their presence in the environment

  19. Silicic volcanism on Mars evidenced by tridymite in high-SiO2 sedimentary rock at Gale crater.

    Science.gov (United States)

    Morris, Richard V; Vaniman, David T; Blake, David F; Gellert, Ralf; Chipera, Steve J; Rampe, Elizabeth B; Ming, Douglas W; Morrison, Shaunna M; Downs, Robert T; Treiman, Allan H; Yen, Albert S; Grotzinger, John P; Achilles, Cherie N; Bristow, Thomas F; Crisp, Joy A; Des Marais, David J; Farmer, Jack D; Fendrich, Kim V; Frydenvang, Jens; Graff, Trevor G; Morookian, John-Michael; Stolper, Edward M; Schwenzer, Susanne P

    2016-06-28

    Tridymite, a low-pressure, high-temperature (>870 °C) SiO2 polymorph, was detected in a drill sample of laminated mudstone (Buckskin) at Marias Pass in Gale crater, Mars, by the Chemistry and Mineralogy X-ray diffraction instrument onboard the Mars Science Laboratory rover Curiosity The tridymitic mudstone has ∼40 wt.% crystalline and ∼60 wt.% X-ray amorphous material and a bulk composition with ∼74 wt.% SiO2 (Alpha Particle X-Ray Spectrometer analysis). Plagioclase (∼17 wt.% of bulk sample), tridymite (∼14 wt.%), sanidine (∼3 wt.%), cation-deficient magnetite (∼3 wt.%), cristobalite (∼2 wt.%), and anhydrite (∼1 wt.%) are the mudstone crystalline minerals. Amorphous material is silica-rich (∼39 wt.% opal-A and/or high-SiO2 glass and opal-CT), volatile-bearing (16 wt.% mixed cation sulfates, phosphates, and chlorides-perchlorates-chlorates), and has minor TiO2 and Fe2O3T oxides (∼5 wt.%). Rietveld refinement yielded a monoclinic structural model for a well-crystalline tridymite, consistent with high formation temperatures. Terrestrial tridymite is commonly associated with silicic volcanism, and detritus from such volcanism in a "Lake Gale" catchment environment can account for Buckskin's tridymite, cristobalite, feldspar, and any residual high-SiO2 glass. These cogenetic detrital phases are possibly sourced from the Gale crater wall/rim/central peak. Opaline silica could form during diagenesis from high-SiO2 glass, as amorphous precipitated silica, or as a residue of acidic leaching in the sediment source region or at Marias Pass. The amorphous mixed-cation salts and oxides and possibly the crystalline magnetite (otherwise detrital) are primary precipitates and/or their diagenesis products derived from multiple infiltrations of aqueous solutions having variable compositions, temperatures, and acidities. Anhydrite is post lithification fracture/vein fill. PMID:27298370

  20. Temporal changes in abundance and composition of ammonia-oxidizing bacterial and archaeal communities in a drained peat soil in relation to N{sub 2}O emissions

    Energy Technology Data Exchange (ETDEWEB)

    Andert, Janet [Swedish Univ. of Agricultural Sciences, Uppsala (Sweden). Dept. of Microbiology; Max-Planck-Institute of Colloids and Interfaces, Potsdam (Germany); Wessen, Ella; Hallin, Sara [Swedish Univ. of Agricultural Sciences, Uppsala (Sweden). Dept. of Microbiology; Boerjesson, Gunnar [Swedish Univ. of Agricultural Sciences, Uppsala (Sweden). Dept. of Soil and Environment

    2011-12-15

    Boreal peat soils comprise about 3% of the terrestrial environments, and when drained, they become sources of the greenhouse gas nitrous oxide (N{sub 2}O). Ammonia oxidation can result in N{sub 2}O emissions, either directly or by fuelling denitrification, but we know little about the ecology of ammonia-oxidizing bacteria (AOB) and archaea (AOA) in peat soils. Our aim was to determine temporal alterations in abundance and composition of these communities in a drained and forested peat soil in relation to N{sub 2}O emissions and ammonia oxidation activity. Materials and methods The peat was sampled at three different depths in the upper 0.5 m over a period of 9 months covering two summer and two winter samplings. Community composition and abundance were determined by T-RFLP and quantitative real-time PCR of the bacterial and archaeal amoA genes. Potential ammonia oxidation rates were measured using the chlorate inhibition technique, and in situ N{sub 2}O emission was determined using chambers. Results and discussion The soil parameters displayed little spatial and temporal heterogeneity, which probably explained why there were no depth-related effects on the abundance, composition, or activity of the ammonia oxidizers. In contrast to most terrestrial environments, the AOB dominated numerically over the AOA. Both groups changed in community composition between sampling occasions, although the AOB showed more significant seasonal signatures than the AOA. Temporal changes in abundance were only observed for the AOB, with a decrease in numbers from May to March. Such differences were not reflected by the activity or N{sub 2}O emissions. Conclusions The high ammonium concentrations in the peat soil likely favored the AOB over the AOA, and we hypothesize that they were more active than the AOA and therefore responded to climatic and environmental changes. However, other processes rather than ammonia oxidation were likely responsible for N{sub 2}O emissions at the site.

  1. Characterization of dissolved organic material in the interstitial brine of Lake Vida, Antarctica

    Science.gov (United States)

    Cawley, Kaelin M.; Murray, Alison E.; Doran, Peter T.; Kenig, Fabien; Stubbins, Aron; Chen, Hongmei; Hatcher, Patrick G.; McKnight, Diane M.

    2016-06-01

    Lake Vida (LV) is located in the McMurdo Dry Valleys (Victoria Valley, East Antarctica) and has no inflows, outflows, or connectivity to the atmosphere due to a thick (16 m), turbid ice surface and cold (salty, dilute low molecular weight fraction. This analytical path resulted in three, low salt sub-fractions and allowed comparison to other Antarctic lake DOM samples isolated using similar procedures. Compared to other Antarctic lakes, a lower portion of the DOC was retained by XAD-8 (∼10% vs. 16-24%) resin, while the portions retained by XAD-4 (∼8%) resin and the 1 kDa ultrafiltration membrane (∼50%) were similar. The 14C radiocarbon ages of the XAD-8 (mean 3940 ybp), XAD-4 (mean 4048 ybp) and HMW (mean 3270 ybp) fractions are all older than the apparent age of ice-cover formation (2800 ybp). Ultrahigh resolution mass spectrometry showed that compounds with two and three nitrogen atoms in the molecular formulas were common in both the LV-XAD8 and LV-XAD4 fractions, consistent with microbial production and processing. The long-term oxidation of LVBr DOM by abiotic oxidants including perchlorate and chlorate may explain the low portion in the XAD8 fraction and the lack of aromatic carbon, as measured by 13C NMR spectroscopy, found for all but the most hydrophobic fraction, LV-XAD8. Overall, the chemical characteristics of Lake Vida brine DOM suggest that legacy DOM sealed and concentrated within the brine has been altered due to a combination of both biological and abiotic chemical reactions.

  2. The use of image analysis for the interaction of 1,3,5-trisubstituted isocyanurates with oxidizer and different binders in composite materials

    Directory of Open Access Journals (Sweden)

    Dostanić Jasmina

    2006-01-01

    Full Text Available Composite propellants are non-homogenous propellants and comprise primarily crystalline oxidizer and metal fuels uniformly suspended in a resin binder. The strength of the bonds between the polymer matrix and the oxidizer determine the mechanical properties of composite propellants. In order to achieve good mechanical properties of the fuel, bonding agents are added to the mixture. The role of the bonding agents is to enable good interactions (interphase between the polymer matrix and the oxidizer grains. The level of interconnection between the phases could be measured by using the surface obtained by cutting the composite material and observing the resulting surface. A problem in the visualization of such a material is to enable the visibility of the polymer matrix and the grains in the image as both phases are white. There are two possible ways to overcome this problem: to add a pigment into the matrix polymer and to color the matrix and make it different from the grain color. Another possibility is to find a solvent for one of the phases and to dissolve one of the phases in an appropriate solvent so that the remaining phase could be stained, photographed and analyzed using the image analysis program. The morphological characteristics of the image could be established and analyzed. The topic of this study was to establish the conditions of preparation of composite propellants containing ammonium per chlorate and HMX and RDX as oxidizers, and polymer of the polybutadiene type and 1,3,5-trisubstituted isocyanurates as bonding agents. The bonding phenomenon was investigated by optical microscopy. The established procedure of preparation will enable the visualization of the composite structure and the morphological characteristics of the surface will be obtained. From the morphological properties of the obtained composite, it will be possible to select a suitable polymer for the preparation of uniformly distributed composite propellant.

  3. Perchlorate and Volatiles of the Brine of Lake Vida (Antarctica): Implication for the in Situ Analysis of Mars Sediments

    Science.gov (United States)

    Kenig, Fabien; Chou, Luoth; McKay, Christopher P.; Jackson, W. Andrew; Doran, Peter T.; Murray, Alison E.; Fritsen, Christian H.

    2016-01-01

    The cold (-13.4 C), cryoencapsulated, anoxic, interstitial brine of the 27 m-thick ice of Lake Vida (Victoria Valley, Antarctica) contains 49 microgram L-1 of perchlorate and 11 microgram L-1 of chlorate. Lake Vida brine (LVBr) may provide an analog for potential oxychlorine-rich subsurface brine on Mars. LVBr volatiles were analyzed by solid-phase microextraction (SPME) gas chromatography-mass spectrometry (GC-MS) with two different SPME fibers. With the exception of volatile organic sulfur compounds, most other volatiles observed were artifacts produced in the GC injector when the thermal decomposition products of oxychlorines reacted with reduced carbon derived from LVBr and the SPME fiber phases. Analysis of MilliQ water with perchlorate (40 microgram L-1) showed low level of organic artifacts, reflecting carbon limitation. In order to observe sample-derived organic compounds, both in analog samples and on Mars, the molar abundance of reduced carbon in a sample must exceed those of O2 and Cl2 produced during decomposition of oxychlorines. This suggests that the abundance of compounds observed by the Sample Analysis at Mars (SAM) instruments in Sheepbed samples (CB-3, CB5, and CB6) may be controlled by an increase in the reduced-carbon/oxychlorine ratio of these samples. To increase chances of in situ detection of Martian organics during pyrolysis-GC-MS, we propose that the derivatization agents stored on SAM may be used as an external source of reduced carbon, increasing artificially the reduced-carbon to perchlorate ratio during pyrolysis, allowing the expression of more abundant and perhaps more diverse Martian organic matter.

  4. Properties of the periplasmic ModA molybdate-binding protein of Escherichia coli.

    Science.gov (United States)

    Rech, S; Wolin, C; Gunsalus, R P

    1996-02-01

    The modABCD operon, located at 17 min on the Escherichia coli chromosome, encodes the protein components of a high affinity molybdate uptake system. Sequence analysis of the modA gene (GenBank L34009) predicts that it encodes a periplasmic binding protein based on the presence of a leader-like sequence at its N terminus. To examine the properties of the ModA protein, the modA structural gene was overexpressed, and its product was purified. The ModA protein was localized to the periplasmic space of the cell, and it was released following a gentle osmotic shock. The N-terminal sequence of ModA confirmed that a leader region of 24 amino acids was removed upon export from the cell. The apparent size of ModA is 31.6 kDa as determined by gel sieve chromatography, whereas it is 22.5 kDa when examined by SDS-polyacrylamide gel electrophoresis. A ligand-dependent protein mobility shift assay was devised using a native polyacrylamide gel electrophoresis protocol to examine binding of molybdate and other anions to the ModA periplasmic protein. Whereas molybdate and tungstate were bound with high affinity (approximately 5 microM), sulfate, chromate, selenate, phosphate, and chlorate did not bind even when tested at 2 mM. A UV spectral assay revealed apparent Kd values of binding for molybdate and tungstate of 3 and 7 microM, respectively. Strains defective in the modA gene were unable to transport molybdate unless high levels of the anion were supplied in the medium. Therefore the modA gene product is essential for high affinity molybdate uptake by the cell. Tungstate interference of molybdate acquisition by the cell is apparently due in part to the high affinity of the ModA protein for this anion.

  5. Molecular analysis of microbial community in a groundwater sample polluted by landfill leachate and seawater

    Institute of Scientific and Technical Information of China (English)

    TIAN Yang-jie; YANG Hong; WU Xiu-juan; LI Dao-tang

    2005-01-01

    Seashore landfill aquifers are environments of special physicochemical conditions (high organic load and high salinity), and microbes in leachate-polluted aquifers play a significant role for intrinsic bioremediation. In order to characterize microbial diversity and look for clues on the relationship between microbial community structure and hydrochemistry, a culture-independent examination of a typical groundwater sample obtained from a seashore landfill was conducted by sequence analysis of 16S rDNA clone library. Two sets of universal 16S rDNA primers were used to amplify DNA extracted from the groundwater so that problems arising from primer efficiency and specificity could be reduced. Of 74 clones randomly selected from the libraries, 30 contained unique sequences whose analysis showed that the majority of them belonged to bacteria (95.9%), with Proteobacteria (63.5%) being the dominant division. One archaeal sequence and one eukaryotic sequence were found as well. Bacterial sequences belonging to the following phylogenic groups were identified: Bacteroidetes (20.3%), β, γ, δ and ε-subdivisions of Proteobacteria (47.3%, 9.5%, 5.4% and 1.3%, respectively), Firmicutes (1.4%), Actinobacteria (2.7%), Cyanobacteria (2.7%). The percentages of Proteobacteria and Bacteroides in seawater were greater than those in the groundwater from a non-seashore landfill, indicating a possible influence of seawater. Quite a few sequences had close relatives in marine or hypersaline environments. Many sequences showed affiliations with microbes involved in anaerobic fermentation. The remarkable abundance of sequences related to (per)chlorate-reducing bacteria (C1RB) in the groundwater was significant and worthy of further study.

  6. Nitrification Potential of Mud Sediment of the Ariake Sea Tidal Flat and the Individual Effect of Temperature, pH, Salinity and Ammonium Concentration on its Nitrification Rate

    Directory of Open Access Journals (Sweden)

    Alim Isnansetyo

    2011-08-01

    Full Text Available The aims of this study were to know the nitrification potential of the mud sediment of the Ariake sea tidal flat, and to investigate the individual influence of environmental parameters such as temperature, pH, salinity and ammonium concentration on its nitrification rate. The Ariake Sea is a semi-closed shallow sea with macro-tidal and the largest tidal flat in Japan. Nitrification Potential Rate (NPR and Nitrification Rate (NR of the tidal flat mud sediment were determined by amending sodium chlorate to inhibit the oxidation of NO2-N to NO3-N. NPRs of the sediment were 91.4, 71.2 and 64.8 nmol N/g Dry Weight Sediment (DWS/h at the depth of 0-3, 3-6 and 6-9 cm, respectively. NRs were relatively high in the temperatures range of 20-35oC with the optimum temperature of 29.3oC. Relatively high NRs were determined in the range of pHs 7.5-8 with the optimum pH 7.7. The optimum salinity for nitrification was 15 ppt. NRs increased drastically in the range of salinity 10 to 15 ppt, but it decreased sharply at 15 to 20 ppt. Relationship between ammonium concentration and NR resulted a hyperbolic Michaëlis-Menten type curve (R2 = 0.98 with the maximum NR rate (Vmax 32.5 nmol N/g DWS/h at NH4-N concentration 3,000 mM and the half saturation constant (Ks 700 mM NH4-N. To our knowledge, this is the first report on nitrification of mud sediment of the Ariake sea tidal flat, and its optimal temperature, pH, salinity and NH4-N concentration as a single parameter.

  7. Study of consumer fireworks post-blast residues by ATR-FTIR.

    Science.gov (United States)

    Martín-Alberca, Carlos; Zapata, Félix; Carrascosa, Héctor; Ortega-Ojeda, Fernando E; García-Ruiz, Carmen

    2016-03-01

    Specific analytical procedures are requested for the forensic analysis of pre- and post-blast consumer firework samples, which present significant challenges. Up to date, vibrational spectroscopic techniques such as Fourier transform infrared spectroscopy (FTIR) have not been tested for the analysis of post-blast residues in spite of their interesting strengths for the forensic field. Therefore, this work proposes a simple and fast procedure for the sampling and analysis of consumer firework post-blast residues by a portable FTIR instrument with an Attenuated Total Reflection (ATR) accessory. In addition, the post-blast residues spectra of several consumer fireworks were studied in order to achieve the identification of their original chemical compositions. Hence, this work analysed 22 standard reagents usually employed to make consumer fireworks, or because they are related to their combustion products. Then, 5 different consumer fireworks were exploded, and their residues were sampled with dry cotton swabs and directly analysed by ATR-FTIR. In addition, their pre-blast fuses and charges were also analysed in order to stablish a proper comparison. As a result, the identification of the original chemical compositions of the post-blast samples was obtained. Some of the compounds found were potassium chlorate, barium nitrate, potassium nitrate, potassium perchlorate or charcoal. An additional study involving chemometric tools found that the results might greatly depend on the swab head type used for the sampling, and its sampling efficiency. The proposed procedure could be used as a complementary technique for the analysis of consumer fireworks post-blast residues. PMID:26717839

  8. 铅阳极泥中有价金属的分离研究%Research on Separation of Valued Metals from Lead Anode Slime

    Institute of Scientific and Technical Information of China (English)

    吴文花; 刘吉波; 王志坚; 苏正夫

    2013-01-01

    After natural stacking oxidation,lead anode slime was leached with potential controlled at 80 ℃ for four hours in medium of 5 mol/L sulfuric acid added with sodium chloride (c(Cl-) =3 mol/L) and oxidant of sodium chlorate with ratio of solid to liquid of 5 ∶ 1.The results show that the leaching rates of copper,bismuth,antimony and arsenic are all above 99%,the leaching rate of tellurium is above 97%,and the leaching rates of gold and silver are below 1% under the potential controlled leaching conditions including stacking duration of lead anode slime of over 4 days,oxidant dosage of >20%,and potential of 40~500 mV.Copper,bismuth,antimony,arsenic and tellurium are successfully separated from gold and silver.%铅阳极泥经过自然堆放氧化后,在5 mol/L硫酸介质中加入一定量的氯化钠(c(Cl-)=3 mol/L)和氧化剂氯酸钠,液固比为5∶1,80℃控制电位氧化浸出4h.结果表明,当铅阳极泥堆放氧化4天以上,氧化剂用量大于20%,电位400~500 mV时,铜、铋、锑、砷的浸出率均在99%以上,碲浸出率大于97%,金、银入液损失均小于1%,很好地实现了铜、铋、锑、砷、碲与金、银的分离.

  9. Silicic volcanism on Mars evidenced by tridymite in high-SiO2 sedimentary rock at Gale crater

    Science.gov (United States)

    Morris, Richard V.; Vaniman, David T.; Blake, David F.; Gellert, Ralf; Chipera, Steve J.; Rampe, Elizabeth B.; Ming, Douglas W.; Morrison, Shaunna M.; Downs, Robert T.; Treiman, Allan H.; Yen, Albert S.; Grotzinger, John P.; Achilles, Cherie N.; Bristow, Thomas F.; Crisp, Joy A.; Des Marais, David J.; Farmer, Jack D.; Fendrich, Kim V.; Graff, Trevor G.; Morookian, John-Michael; Stolper, Edward M.; Schwenzer, Susanne P.

    2016-01-01

    Tridymite, a low-pressure, high-temperature (>870 °C) SiO2 polymorph, was detected in a drill sample of laminated mudstone (Buckskin) at Marias Pass in Gale crater, Mars, by the Chemistry and Mineralogy X-ray diffraction instrument onboard the Mars Science Laboratory rover Curiosity. The tridymitic mudstone has ∼40 wt.% crystalline and ∼60 wt.% X-ray amorphous material and a bulk composition with ∼74 wt.% SiO2 (Alpha Particle X-Ray Spectrometer analysis). Plagioclase (∼17 wt.% of bulk sample), tridymite (∼14 wt.%), sanidine (∼3 wt.%), cation-deficient magnetite (∼3 wt.%), cristobalite (∼2 wt.%), and anhydrite (∼1 wt.%) are the mudstone crystalline minerals. Amorphous material is silica-rich (∼39 wt.% opal-A and/or high-SiO2 glass and opal-CT), volatile-bearing (16 wt.% mixed cation sulfates, phosphates, and chlorides−perchlorates−chlorates), and has minor TiO2 and Fe2O3T oxides (∼5 wt.%). Rietveld refinement yielded a monoclinic structural model for a well-crystalline tridymite, consistent with high formation temperatures. Terrestrial tridymite is commonly associated with silicic volcanism, and detritus from such volcanism in a “Lake Gale” catchment environment can account for Buckskin’s tridymite, cristobalite, feldspar, and any residual high-SiO2 glass. These cogenetic detrital phases are possibly sourced from the Gale crater wall/rim/central peak. Opaline silica could form during diagenesis from high-SiO2 glass, as amorphous precipitated silica, or as a residue of acidic leaching in the sediment source region or at Marias Pass. The amorphous mixed-cation salts and oxides and possibly the crystalline magnetite (otherwise detrital) are primary precipitates and/or their diagenesis products derived from multiple infiltrations of aqueous solutions having variable compositions, temperatures, and acidities. Anhydrite is post lithification fracture/vein fill. PMID:27298370

  10. Tyrosine sulfation of the amino terminus of PSGL-1 is critical for enterovirus 71 infection.

    Directory of Open Access Journals (Sweden)

    Yorihiro Nishimura

    Full Text Available Enterovirus 71 (EV71 is one of the major causative agents of hand, foot, and mouth disease, a common febrile disease in children; however, EV71 has been also associated with various neurological diseases including fatal cases in large EV71 outbreaks particularly in the Asia Pacific region. Recently we identified human P-selectin glycoprotein ligand-1 (PSGL-1 as a cellular receptor for entry and replication of EV71 in leukocytes. PSGL-1 is a sialomucin expressed on the surface of leukocytes, serves as a high affinity counterreceptor for selectins, and mediates leukocyte rolling on the endothelium. The PSGL-1-P-selectin interaction requires sulfation of at least one of three clustered tyrosines and an adjacent O-glycan expressing sialyl Lewis x in an N-terminal region of PSGL-1. To elucidate the molecular basis of the PSGL-1-EV71 interaction, we generated a series of PSGL-1 mutants and identified the post-translational modifications that are critical for binding of PSGL-1 to EV71. We expressed the PSGL-1 mutants in 293T cells and the transfected cells were assayed for their abilities to bind to EV71 by flow cytometry. We found that O-glycosylation on T57, which is critical for PSGL-1-selectin interaction, is not necessary for PSGL-1 binding to EV71. On the other hand, site-directed mutagenesis at one or more potential tyrosine sulfation sites in the N-terminal region of PSGL-1 significantly impaired PSGL-1 binding to EV71. Furthermore, an inhibitor of sulfation, sodium chlorate, blocked the PSGL-1-EV71 interaction and inhibited PSGL-1-mediated viral replication of EV71 in Jurkat T cells in a dose-dependent manner. Thus, the results presented in this study reveal that tyrosine sulfation, but not O-glycosylation, in the N-terminal region of PSGL-1 may facilitate virus entry and replication of EV71 in leukocytes.

  11. NasR, a novel RNA-binding protein, mediates nitrate-responsive transcription antitermination of the Klebsiella oxytoca M5al nasF operon leader in vitro.

    Science.gov (United States)

    Chai, W; Stewart, V

    1998-10-23

    In Klebsiella oxytoca (pneumoniae), enzymes required for nitrate assimilation are encoded by the nasFEDCBA operon. Previous genetic studies led to the conclusion that nitrate and nitrite induction of nasF operon expression is determined by a transcriptional antitermination mechanism. In the presence of nitrate or nitrite, the nasR gene product is hypothesized to inhibit transcription termination at the factor-independent terminator site located in the nasF operon leader region. To test this model in vitro, we first purified NasR as both a maltose binding protein fusion form (MBP-NasR) and a His6-tagged form (His6-NasR). Templates for in vitro transcription contained the nasF operon leader region, with a substitution of the sigma70-dependent tac promoter for the native sigmaN-dependent promoter. We found that in vitro transcription of the leader template terminated at the terminator site, and that MBP-NasR and His6-NasR proteins both caused transcription readthrough of this site in response to nitrate or nitrite. Half-maximal antitermination required nitrate or nitrite at moderate (1 to 10 microM) concentrations, and several other anions tested, including chlorate, were without effect. Previous in vivo analysis of leader deletions identified regions required for both negative regulation (the terminator) and for positive regulation. Results from in vitro transcription of these deletion templates correlated fully with the in vivo analysis. Finally, electrophoresis mobility shift analysis revealed that His6-NasR bound specifically to nasF leader RNA. This binding was independent of nitrate in vitro. These results strongly support the conclusions drawn from previous in vivo analysis, and establish that NasR mediates ligand-responsive transcription antitermination through interaction with nasF leader RNA. PMID:9769209

  12. Identification and determination of inorganic anions in real extracts from pre- and post-blast residues by capillary electrophoresis.

    Science.gov (United States)

    Sarazin, Cédric; Delaunay, Nathalie; Varenne, Anne; Vial, Jérôme; Costanza, Christine; Eudes, Véronique; Minet, Jean-Jacques; Gareil, Pierre

    2010-10-29

    Fast, selective, and sensitive analysis of inorganic anions is compulsory for the identification of explosives in post-blast or environmental samples. For the last twenty years, capillary electrophoresis (CE) has become a valuable alternative to ion chromatography (IC) for the analysis of inorganic-based explosives because of its low running costs and its simplicity of use. This article focuses on the development and validation of a CE method for the simultaneous analysis of 10 anions (chloride, nitrite, nitrate, thiosulphate, perchlorate, chlorate, thiocyanate, carbonate, sulphate, and phosphate) which can be found in post-blast residues, plus for the first time azide anion, possibly present in the composition of detonators, and the internal standard (formate) in 20 min total runtime. Intermediate precisions were 2.11% for normalized areas and 0.72% for normalized migration times. Limits of detection close to 0.5 ppm for all anions were obtained with the use of preconcentration techniques, thanks to a fast and simple sample preparation allowing the analysis of a large variety of matrices with the developed generic CE method. The matrix effects were statistically studied for the first time in the explosive field for different matrices, containing interfering anions and cations, sometimes at high levels. In fact, no significant matrix effect occurred (tests with blank matrix extracts of soil, cloth, glass, plastic, paper, cotton, and metal). Finally, analyses of real post-blast residues and real detonator extracts were performed. The CE results were compared with those obtained with the IC method used routinely and showed excellent correlation.

  13. Final Technical Report: Genetic Control of Nitrogen Assimilation in Klebsiella oxytoca.

    Energy Technology Data Exchange (ETDEWEB)

    Valley Stewart

    2007-03-07

    Klebsiella oxytoca, an enterobacterium closely related to Escherichia coli and amenable to molecular genetic analysis, is a long-established model organism for studies of bacterial nitrogen assimilation. Our work concerned utilization of purines, nitrogen-rich compounds that are widespread in the biosphere. This project began with our observation that molybdenum cofactor (chlorate-resistant) mutants can use (hypo)xanthine as sole nitrogen source (Garzón et al., J. Bacteriol. 174:6298, 1992). Since xanthine dehydrogenase is a molybdoenzyme, Klebsiella must use an alternate route for (hypo)xanthine catabolsim. We identified and characterized a cluster of 22 genes that encode the enzymes, permeases and regulators for utilizing hypoxanthine and xanthine as sole nitrogen source. (Hypoxanthine and xanthine arise from deamination of adenine and guanine, respectively.) Growth and complementation tests with insertion mutants, combined with protein sequence comparisons, allow us to assign probable functions for the products of these genes and to deduce the overall pathway. We present genetic evidence that the first two enzymes for the Klebsiella purine utilization pathway have been recruited from pathways involved in catabolism of aromatic compounds. The first, HxaAB enzyme catalyzing (hypo)xanthine oxidation, is related to well-studied aromatic ring hydroxylating oxygenases such as phthalate dioxygenase. The second, HxbA enzyme catalyzing urate hydroxylation, is related to single-component monooxygenases. Thus, the Klebsiella purine utilization pathway has likely experienced non-orthologous gene displacement, substituting these oxygenases for the conventional enzymes, xanthine dehydrogenase and uricase. We also present evidence that transcription of the hxaAB operon is subject to dual regulation: global general nitrogen regulation (Ntr) through an unknown mechanism, and (hypo)xanthine induction mediated by a LysR-type activator.

  14. Clinical application of therapeutic erythrocytapheresis (TEA).

    Science.gov (United States)

    Valbonesi, M; Bruni, R

    2000-06-01

    Therapeutic erythrocytapheresis (TEA) has been used in different diseases such as polycythemia vera (PV), secondary erythrocytosis or hemochromatosis as a process of the less cumbersome but more expensive phlebotomy. TEA is preferred in emergency conditions such as thrombocytosis or in conditions such as porphyria cutanea tarda (PCT) or erythropoietic porphyria when plasma exchange (PEX) is often combined with TEA to reduce extracellular levels of uroporphyrin which contribute to plasma hyperviscosity. TEA is often combined with drug therapy that varies from etoposide in PV to EPO and desferoxamine which are used to mobilize and reduce iron stores in hemochromatosis. Benefits from this combination may be more long lasting than expected. Nonetheless for TEA, there is no standard protocol and, clinical experience with this therapy remains highly anecdotal. Therapeutic red cell-exchange (TREX) has been used with much interest over the years, starting with the management of hemolytic disease of the newborn and later used to correct severe anemia in thalassemia patients thereby preventing iron overload. It has also been used for the management of complications of sickle cell disease such as priapism, chest syndrome, stroke, retinal, bone, splenic and hepatic infarction or in preparation for surgery by reducing HbS to less than 30%. Automated apheresis has also favored the use of TREX in conditions such as paroxysmal nocturnal hemoglobinuria and aniline poisoning, arsenic poisoning, Na chlorate intoxications and CO intoxications, hemoglobinopathies, autoimmune hemolytic anemia, reactions due to ABO incompatibility, in preparation for ABO incompatible bone marrow transplantation or for preventing anti-D immunization after the transfusion of D(+) cells to D(-) recipients. Another field of application has been in the emergency management of intraerythrocytic parasite infections such as malaria and babesiosis. Application of TREX may be wide but its real use remains limited

  15. Identification of improvised explosives residues using physical-chemical analytical methods under real conditions after an explosion

    Science.gov (United States)

    Kotrlý, Marek; Mareš, Bohumil; Turková, Ivana; Beroun, Ivo

    2016-05-01

    Within the analysis of cases relating to the use of explosives for crimes, we have experienced a shift from using industrial explosives towards substances made in amateur and illegal way. Availability of industrial explosives is increasingly limited to a narrow sphere of subjects with a relevant permission. Thus, on the part of perpetrators, terrorists, ever greater attention is paid to illegal production of explosives that are easily made from readily available raw materials. Another alarming fact is the availability of information found on the internet. Procedures of preparation are often very simple and do not require even a deeper professional knowledge. Explosive characteristics are not actually accessible for many of these substances (detonation velocity, sensitivity, working capacity, brisance, physical and chemical stability, etc.). Therefore, a project is being implemented, which on grounds of assessment of individual information available in literature and on the internet, aiming at choosing individual areas of potentially abusable substances (e.g. mixtures of nitric acid (98%) with organic substances, mixtures nitromethane and tetranitromethane with organic substances, mixtures of chlorates and perchlorates of alkali metals with organic substances, chemically individual compounds of organic base type of perchloric acid, azides, fulminates, acetylides, picrates, styphnates of heavy metals, etc.). It is directed towards preparation of these explosives also in non-stoichiometric mixtures, conducting test explosives, determination of explosive characteristics (if they are unknown) and analysis of both primary phases and post-blast residues through available analytical techniques, such as gas and liquid chromatography with mass detection, FTIR, micro-Raman spectrometry, electron microscopy with microanalysis and Raman microspectrometry directly in SEM chamber for analysis at the level of individual microparticles. The received characteristics will be used to

  16. Identification of inorganic improvised explosive devices using sequential injection capillary electrophoresis and contactless conductivity detection.

    Science.gov (United States)

    Blanco, Gustavo A; Nai, Yi H; Hilder, Emily F; Shellie, Robert A; Dicinoski, Greg W; Haddad, Paul R; Breadmore, Michael C

    2011-12-01

    A simple sequential injection capillary electrophoresis (SI-CE) instrument with capacitively coupled contactless conductivity detection (C(4)D) has been developed for the rapid separation of anions relevant to the identification of inorganic improvised explosive devices (IEDs). Four of the most common explosive tracer ions, nitrate, perchlorate, chlorate, and azide, and the most common background ions, chloride, sulfate, thiocyanate, fluoride, phosphate, and carbonate, were chosen for investigation. Using a separation electrolyte comprising 50 mM tris(hydroxymethyl)aminomethane, 50 mM cyclohexyl-2-aminoethanesulfonic acid, pH 8.9 and 0.05% poly(ethyleneimine) (PEI) in a hexadimethrine bromide (HDMB)-coated capillary it was possible to partially separate all 10 ions within 90 s. The combination of two cationic polymer additives (PEI and HDMB) was necessary to achieve adequate selectivity with a sufficiently stable electroosmotic flow (EOF), which was not possible with only one polymer. Careful optimization of variables affecting the speed of separation and injection timing allowed a further reduction of separation time to 55 s while maintaining adequate efficiency and resolution. Software control makes high sample throughput possible (60 samples/h), with very high repeatability of migration times [0.63-2.07% relative standard deviation (RSD) for 240 injections]. The separation speed does not compromise sensitivity, with limits of detection ranging from 23 to 50 μg·L(-1) for all the explosive residues considered, which is 10× lower than those achieved by indirect absorbance detection and 2× lower than those achieved by C(4)D using portable benchtop instrumentation. The combination of automation, high sample throughput, high confidence of peak identification, and low limits of detection makes this methodology ideal for the rapid identification of inorganic IED residues.

  17. Silicic volcanism on Mars evidenced by tridymite in high-SiO2 sedimentary rock at Gale crater

    Science.gov (United States)

    Morris, Richard V.; Vaniman, David T.; Blake, David F.; Gellert, Ralf; Chipera, Steve J.; Rampe, Elizabeth B.; Ming, Douglas W.; Morrison, Shaunna M.; Downs, Robert T.; Treiman, Allan H.; Yen, Albert S.; Grotzinger, John P.; Achilles, Cherie N.; Bristow, Thomas F.; Crisp, Joy A.; Des Marais, David J.; Farmer, Jack D.; Fendrich, Kim V.; Frydenvang, Jens; Graff, Trevor G.; Morookian, John-Michael; Stolper, Edward M.; Schwenzer, Susanne P.

    2016-06-01

    Tridymite, a low-pressure, high-temperature (>870 °C) SiO2 polymorph, was detected in a drill sample of laminated mudstone (Buckskin) at Marias Pass in Gale crater, Mars, by the Chemistry and Mineralogy X-ray diffraction instrument onboard the Mars Science Laboratory rover Curiosity. The tridymitic mudstone has ˜40 wt.% crystalline and ˜60 wt.% X-ray amorphous material and a bulk composition with ˜74 wt.% SiO2 (Alpha Particle X-Ray Spectrometer analysis). Plagioclase (˜17 wt.% of bulk sample), tridymite (˜14 wt.%), sanidine (˜3 wt.%), cation-deficient magnetite (˜3 wt.%), cristobalite (˜2 wt.%), and anhydrite (˜1 wt.%) are the mudstone crystalline minerals. Amorphous material is silica-rich (˜39 wt.% opal-A and/or high-SiO2 glass and opal-CT), volatile-bearing (16 wt.% mixed cation sulfates, phosphates, and chlorides-perchlorates-chlorates), and has minor TiO2 and Fe2O3T oxides (˜5 wt.%). Rietveld refinement yielded a monoclinic structural model for a well-crystalline tridymite, consistent with high formation temperatures. Terrestrial tridymite is commonly associated with silicic volcanism, and detritus from such volcanism in a “Lake Gale” catchment environment can account for Buckskin's tridymite, cristobalite, feldspar, and any residual high-SiO2 glass. These cogenetic detrital phases are possibly sourced from the Gale crater wall/rim/central peak. Opaline silica could form during diagenesis from high-SiO2 glass, as amorphous precipitated silica, or as a residue of acidic leaching in the sediment source region or at Marias Pass. The amorphous mixed-cation salts and oxides and possibly the crystalline magnetite (otherwise detrital) are primary precipitates and/or their diagenesis products derived from multiple infiltrations of aqueous solutions having variable compositions, temperatures, and acidities. Anhydrite is post lithification fracture/vein fill.

  18. A Cabin Air Separator for EVA Oxygen

    Science.gov (United States)

    Graf, John C.

    2011-01-01

    Presently, the Extra-Vehicular Activities (EVAs) conducted from the Quest Joint Airlock on the International Space Station use high pressure, high purity oxygen that is delivered to the Space Station by the Space Shuttle. When the Space Shuttle retires, a new method of delivering high pressure, high purity oxygen to the High Pressure Gas Tanks (HPGTs) is needed. One method is to use a cabin air separator to sweep oxygen from the cabin air, generate a low pressure/high purity oxygen stream, and compress the oxygen with a multistage mechanical compressor. A main advantage to this type of system is that the existing low pressure oxygen supply infrastructure can be used as the source of cabin oxygen. ISS has two water electrolysis systems that deliver low pressure oxygen to the cabin, as well as chlorate candles and compressed gas tanks on cargo vehicles. Each of these systems can feed low pressure oxygen into the cabin, and any low pressure oxygen source can be used as an on-board source of oxygen. Three different oxygen separator systems were evaluated, and a two stage Pressure Swing Adsorption system was selected for reasons of technical maturity. Two different compressor designs were subjected to long term testing, and the compressor with better life performance and more favorable oxygen safety characteristics was selected. These technologies have been used as the basis of a design for a flight system located in Equipment Lock, and taken to Preliminary Design Review level of maturity. This paper describes the Cabin Air Separator for EVA Oxygen (CASEO) concept, describes the separator and compressor technology trades, highlights key technology risks, and describes the flight hardware concept as presented at Preliminary Design Review (PDR)

  19. Investigation, Analysis, and Testing of Self-contained Oxygen Generators

    Science.gov (United States)

    Keddy, Christopher P.; Haas, Jon P.; Starritt, Larry

    2008-01-01

    Self Contained Oxygen Generators (SCOGs) have widespread use in providing emergency breathing oxygen in a variety of environments including mines, submarines, spacecraft, and aircraft. These devices have definite advantages over storing of gaseous or liquid oxygen. The oxygen is not generated until a chemical briquette containing a chlorate or perchlorate oxidizer and a solid metallic fuel such as iron is ignited starting a thermal decomposition process allowing gaseous oxygen to be produced. These devices are typically very safe to store, easy to operate, and have primarily only a thermal hazard to the operator that can be controlled by barriers or furnaces. Tens of thousands of these devices are operated worldwide every year without major incident. This report examines the rare case of a SCOG whose behavior was both abnormal and lethal. This particular type of SCOG reviewed is nearly identical to a flight qualified version of SCOG slated for use on manned space vehicles. This Investigative Report is a compilation of a NASA effort in conjunction with other interested parties including military and aerospace to understand the causes of the particular SCOG accident and what preventative measures can be taken to ensure this incident is not repeated. This report details the incident and examines the root causes of the observed SCOG behavior from forensic evidence. A summary of chemical and numerical analysis is provided as a background to physical testing of identical SCOG devices. The results and findings of both small scale and full scale testing are documented on a test-by-test basis along with observations and summaries. Finally, conclusions are presented on the findings of this investigation, analysis, and testing along with suggestions on preventative measures for any entity interested in the safe use of these devices.

  20. Effects of Different Oxidants on HCl-based Pickling Process of 430 Stainless Steel

    Institute of Scientific and Technical Information of China (English)

    Qiong XIE; Pei-yang SHI; Cheng-jun LIU; Mao-fa JIANG

    2016-01-01

    To shorten the time required for the pickling process and to enhance the quality of ferritic stainless steel plates,the effects of oxidants including hydrogen peroxide (H2 O2 ),potassium permanganate (KMnO4 ),and potas-sium chlorate (KClO3 )on the pickling behavior in HCl-based electrolyte as well as the surface quality of hot-rolled and blasted 430 stainless steel (430-SS)were studied.Experiments were conducted using mass-loss tests,micro-structure analyses,potentiodynamic polarization curves,and electrochemical impedance spectroscopy measurements. The results showed that the addition of oxidants substantially accelerated the pickling process of 430-SS by enhancing the cathodic reaction rate and reducing the charge transfer resistance.In electrolytes comprising 5-8 mass% HCl at a temperature of 40-60 ℃ and at the same concentration within the range from 0 to 2 mass%,H2 O2 was demon-strated to be superior to KMnO4 and KClO3 in accelerating the pickling process.The surface quality of 430-SS pick-led in the presence of H2 O2 was better than those of specimens pickled in the presence of KMnO4 and KClO3 when the removal of the oxide layer,intergranular corrosion,and surface roughness were collectively considered. When 1 mass% H2 O2 was added,the mass loss rate of 430-SS was increased by 629% and no residual oxide layer or intergranular corrosion was observed on the surface of the steel;in addition,the roughness was only 1.7μm.H2 O2 was determined to be a better oxidant than KMnO4 and KClO3 when the pickling process,surface quality,solution recycling,and environment protection were considered as a whole.

  1. 二氧化氯与氯联合消毒对饮用水中消毒副产物的影响%EFFECT OF COMBINED DISINFECTION WITH CHLORINE AND CHLORINE DIOXIDE ON THE FORMATION OF DISINFECTION BY-PRODUCTS IN DRINKING WATER

    Institute of Scientific and Technical Information of China (English)

    叶必雄; 王五一; 杨林生; 王小龙; 魏建荣

    2011-01-01

    In an effect to explore the production mechanisms and characteristics of the by-products in different water disinfection processes,and to investigate the effect of chlorine dioxide on the formation of chlorine by-products,water samples from 4 water plants in a city in China were analyzed.Compared with the water disinfected with chlorine alone,the amount of THMs and HAAs decreased by 74.39% and 40.65%,respectively,in water samples disinfected with both chlorine dioxide and chlorine.Likewise,the amounts of chlorate and chlorite produced by the chlorine dioxide chemical generator was higher than that of the pure chlorine dioxide generator.%为了研究二氧化氯与氯联合消毒工艺过程中消毒副产物的形成规律以及特点,探讨二氧化氯对氯化消毒副产物的控制效果,对我国北方某市使用同一水源的4家水厂消毒工艺进行全面的采样与检测,并对各项消毒副产物检测结果进行了全面的分析.结果表明,二氧化氯与氯联合消毒比单纯液氯消毒形成的三卤甲烷平均降低74.39%,卤乙酸平均降低40.65%.在控制氯酸盐及亚氯酸盐生成方面,使用纯二氧化氯发生器生成的氯酸盐要显著低于化学法复合二氧化氯发生器.

  2. The relationship between anammox and denitrification in the sediment of an inland river

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Sheng, E-mail: zhous@outlook.com [Eco-environmental Protection Research Institute, Shanghai Academy of Agricultural Sciences, No. 1000 Jinqi Road, Shanghai 201403 (China); Institute of Engineering, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei, Tokyo 184-8588 (Japan); Borjigin, Sodbilig; Riya, Shohei; Terada, Akihiko; Hosomi, Masaaki [Institute of Engineering, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei, Tokyo 184-8588 (Japan)

    2014-08-15

    This study measured the microbial processes of anaerobic ammonium oxidation (anammox) and denitrification in sediment sampled from two sites in the estuary of an inland river (Koisegawa River, Ibaragi prefecture, Japan) using a nitrogen isotope pairing technique (IPT). The responses of anammox and denitrification activities to temperature and nitrate concentration were also evaluated. Further, to elucidate the correlation between anammox and denitrification processes, an inhibition experiment was conducted, using chlorate to inhibit the first step of denitrification. Denitrification activity was much higher than anammox activity, and it reached a maximum at the surface layer in February 2012. Denitrification activity decreased as sediment depth increased, and a similar phenomenon was observed for anammox activity in the sediment of site A, where aquatic plants were absent from the surroundings. The activities of both denitrification and anammox were temperature-dependent, but they responded differently to changes in incubation temperature. Compared to a linear increase in denitrification as temperature rose to 35 °C, the optimal temperature for anammox was 25 °C, after which the activity decreased sharply. At the same time, both anammox and denitrification activities increased with NO{sub 3}{sup −} concentration. The Michaelis–Menten kinetic constants (V{sub max} and K{sub m}) of denitrification were significantly higher than those of the anammox process. Furthermore, anammox activity decreased accordingly when the first step of denitrification was inhibited, which probably reduced the amount of the intermediate NO{sub 2}{sup −}. Our study provides the first direct exploration of the denitrification-dependent correlation of anammox activity in the sediment of inland river. - Highlights: • The activity of denitrification in river sediment was much higher than anammox. • Denitrification and anammox respond differently to changes in temperature.

  3. Methane oxidation linked to chlorite dismutation.

    Directory of Open Access Journals (Sweden)

    Laurence G. Miller

    2014-06-01

    Full Text Available We examined the potential for CH4 oxidation to be coupled with oxygen derived from the dissimilatory reduction of perchlorate, chlorate or via chlorite (ClO2- dismutation. Although dissimilatory reduction of ClO4- and ClO3- could be inferred from the accumulation of chloride ions either in spent media or in soil slurries prepared from exposed freshwater lake sediment, neither of these oxyanions evoked methane oxidation when added to either anaerobic mixed cultures or soil enriched in methanotrophs. In contrast, ClO2- amendment elicited such activity. Methane (0.2 kPa was completely removed within several days from the headspace of cell suspensions of Dechloromonas agitata CKB incubated with either Methylococcus capsulatus Bath or Methylomicrobium album BG8 in the presence of 5 mM ClO2-. We also observed complete removal of 0.2 kPa CH4 in bottles containing soil enriched in methanotrophs when co-incubated with D. agitata CKB and 10 mM ClO2-. However, to be effective these experiments required physical separation of soil from D. agitata CKB to allow for the partitioning of O2 liberated from chlorite dismutation into the shared headspace. Although a link between ClO2- and CH4 consumption was established in soils and cultures, no upstream connection with either ClO4- or ClO3- was discerned. This result suggests that the release of O2 during enzymatic perchlorate reduction was negligible, and that the oxygen produced was unavailable to the aerobic methanotrophs.

  4. Dual chitosan/albumin-coated alginate/dextran sulfate nanoparticles for enhanced oral delivery of insulin.

    Science.gov (United States)

    Lopes, Marlene; Shrestha, Neha; Correia, Alexandra; Shahbazi, Mohammad-Ali; Sarmento, Bruno; Hirvonen, Jouni; Veiga, Francisco; Seiça, Raquel; Ribeiro, António; Santos, Hélder A

    2016-06-28

    The potential of nanoparticles (NPs) to overcome the barriers for oral delivery of protein drugs have led to the development of platforms capable of improving their bioavailability. However, despite the progresses in drug delivery technologies, the success of oral delivery of insulin remains elusive and the disclosure of insulin mechanisms of absorption remains to be clarified. To overcome multiple barriers faced by oral insulin and to enhance the insulin permeability across the intestinal epithelium, here insulin-loaded alginate/dextran sulfate (ADS)-NPs were formulated and dual-coated with chitosan (CS) and albumin (ALB). The nanosystem was characterized by its pH-sensitivity and mucoadhesivity, which enabled to prevent 70% of in vitro insulin release in simulated gastric conditions and allowed a sustained insulin release following the passage to simulated intestinal conditions. The pH and time-dependent morphology of the NPs was correlated to the release and permeation profile of insulin. Dual CS/ALB coating of the ADS-NPs demonstrated augmented intestinal interactions with the intestinal cells in comparison to the uncoated-NPs, resulting in a higher permeability of insulin across Caco-2/HT29-MTX/Raji B cell monolayers. The permeability of the insulin-loaded ALB-NPs was reduced after the temperature was decreased and after co-incubation with chlorpromazine, suggesting an active insulin transport by clathrin-mediated endocytosis. Moreover, the permeability inhibition with the pre-treatment with sodium chlorate suggested that the interaction between glycocalix and the NPs was critical for insulin permeation. Overall, the developed nanosystem has clinical potential for the oral delivery of insulin and therapy of type 1 diabetes mellitus. PMID:27074369

  5. Chloroxyanion Residue Quantification in Cantaloupes Treated with Chlorine Dioxide Gas.

    Science.gov (United States)

    Kaur, Simran; Smith, David J; Morgan, Mark T

    2015-09-01

    Previous studies show that treatment of cantaloupes with chlorine dioxide (ClO2) gas at 5 mg/liter for 10 min results in a significant reduction (P < 0.05) in initial microflora, an increase in shelf life without any alteration in color, and a 4.6- and 4.3-log reduction of Escherichia coli O157:H7 and Listeria monocytogenes, respectively. However, this treatment could result in the presence of chloroxyanion residues, such as chloride (Cl(-)), chlorite (ClO2(-)), chlorate (ClO3(-)), and perchlorate (ClO4(-)), which, apart from chloride, are a toxicity concern. Radiolabeled chlorine dioxide ((36)ClO2) gas was used to describe the identity and distribution of chloroxyanion residues in or on cantaloupe subsequent to fumigation with ClO2 gas at a mean concentration of 5.1 ± 0.7 mg/liter for 10 min. Each treated cantaloupe was separated into rind, flesh, and mixed (rind and flesh) sections, which were blended and centrifuged to give the corresponding sera fractions. Radioactivity detected, ratio of radioactivity to mass of chlorite in initial ClO2 gas generation reaction, and distribution of chloroxyanions in serum samples were used to calculate residue concentrations in flesh, rind, and mixed samples. Anions detected on the cantaloupe were Cl(-) (∼ 90%) and ClO3(-) (∼ 10%), located primarily in the rind (19.3 ± 8.0 μg of Cl(-)/g of rind and 4.8 ± 2.3 μg of ClO3(-)/g of rind, n = 6). Cantaloupe flesh (∼ 200 g) directly exposed to(36)ClO2 gas treatment showed the presence of only Cl(-) residues (8.1 ± 1.0 μg of Cl(-)/g of flesh, n = 3). Results indicate chloroxyanion residues Cl(-) and ClO3(-) are only present on the rind of whole cantaloupes treated with ClO2 gas. However during cutting, residues may be transferred to the fruit flesh. Because Cl(-) is not toxic, only ClO3(-) would be a toxicity concern, but the levels transferred from rind to flesh are very low. In the case of fruit flesh directly exposed to ClO2 gas, only nontoxic Cl(-) was detected. This

  6. Electron transport to periplasmic nitrate reductase (NapA) of Wolinella succinogenes is independent of a NapC protein.

    Science.gov (United States)

    Simon, Jörg; Sänger, Monica; Schuster, Stephan C; Gross, Roland

    2003-07-01

    The rumen bacterium Wolinella succinogenes grows by respiratory nitrate ammonification with formate as electron donor. Whereas the enzymology and coupling mechanism of nitrite respiration is well known, nitrate reduction to nitrite has not yet been examined. We report here that intact cells and cell fractions catalyse nitrate and chlorate reduction by reduced viologen dyes with high specific activities. A gene cluster encoding components of a putative periplasmic nitrate reductase system (napA, G, H, B, F, L, D) was sequenced. The napA gene was inactivated by inserting a kanamycin resistance gene cassette. The resulting mutant did not grow by nitrate respiration and did not reduce nitrate during growth by fumarate respiration, in contrast to the wild type. An antigen was detected in wild-type cells using an antiserum raised against the periplasmic nitrate reductase (NapA) from Paracoccus pantotrophus. This antigen was absent in the W. succinogenes napA mutant. It is concluded that the periplasmic nitrate reductase NapA is the only respiratory nitrate reductase in W. succinogenes, although a second nitrate-reducing enzyme is apparently induced in the napA mutant. The nap cluster of W. succinogenes lacks a napC gene whose product is thought to function in quinol oxidation and electron transfer to NapA in other bacteria. The W. succinogenes genome encodes two members of the NapC/NirT family, NrfH and FccC. Characterization of corresponding deletion mutants indicates that neither of these two proteins is required for nitrate respiration. A mutant lacking the genes encoding respiratory nitrite reductase (nrfHA) had wild-type properties with respect to nitrate respiration. A model of the electron transport chain of nitrate respiration is proposed in which one or more of the napF, G, H and L gene products mediate electron transport from menaquinol to the periplasmic NapAB complex. Inspection of the W. succinogenes genome sequence suggests that ammonia formation from

  7. Enhanced bromate formation during chlorination of bromide-containing waters in the presence of CuO: Catalytic disproportionation of hypobromous acid

    KAUST Repository

    Liu, Chao

    2012-10-16

    Bromate (BrO3 -) in drinking water is traditionally seen as an ozonation byproduct from the oxidation of bromide (Br-), and its formation during chlorination is usually not significant. This study shows enhanced bromate formation during chlorination of bromide-containing waters in the presence of cupric oxide (CuO). CuO was effective to catalyze hypochlorous acid (HOCl) or hypobromous acid (HOBr) decay (e.g., at least 104 times enhancement for HOBr at pH 8.6 by 0.2 g L-1 CuO). Significant halate concentrations were formed from a CuO-catalyzed hypohalite disproportionation pathway. For example, the chlorate concentration was 2.7 ± 0.2 μM (225.5 ± 16.7 μg L-1) after 90 min for HOCl (Co = 37 μM, 2.6 mg L-1 Cl2) in the presence of 0.2 g L-1 CuO at pH 7.6, and the bromate concentration was 6.6 ± 0.5 μM (844.8 ± 64 μg L -1) after 180 min for HOBr (Co = 35 μM) in the presence of 0.2 g L-1 CuO at pH 8.6. The maximum halate formation was at pHs 7.6 and 8.6 for HOCl or HOBr, respectively, which are close to their corresponding pKa values. In a HOCl-Br--CuO system, BrO3 - formation increases with increasing CuO doses and initial HOCl and Br- concentrations. A molar conversion (Br - to BrO3 -) of up to (90 ± 1)% could be achieved in the HOCl-Br--CuO system because of recycling of Br - to HOBr by HOCl, whereas the maximum BrO3 - yield in HOBr-CuO is only 26%. Bromate formation is initiated by the formation of a complex between CuO and HOBr/OBr-, which then reacts with HOBr to generate bromite. Bromite is further oxidized to BrO3 - by a second CuO-catalyzed process. These novel findings may have implications for bromate formation during chlorination of bromide-containing drinking waters in copper pipes. © 2012 American Chemical Society.

  8. Influence of ultrasound enhancement on chlorine dioxide consumption and disinfection by-products formation for secondary effluents disinfection.

    Science.gov (United States)

    Zhou, Xiaoqin; Zhao, Junyuan; Li, Zifu; Lan, Juanru; Li, Yajie; Yang, Xin; Wang, Dongling

    2016-01-01

    Chlorine dioxide (ClO2) has been promoted as an alternative disinfectant because of its high disinfection efficiency and less formation of organic disinfection by-products (DBPs). However, particle-associated microorganisms could be protected during the disinfection process, which decreases the disinfection efficiency or increases the required dosage. Besides, the formation of inorganic disinfection by-products is a significant concern in environment health. Ultrasound (US)-combined disinfection methods are becoming increasingly attractive because they are efficient and environmentally friendly. In this study, US was introduced as an enhancement method to identify its influence on ClO2 demand reduction and to minimize the production of potential DBPs for secondary effluents disinfection. Fecal coliform was used as an indicator, and DBPs, including trichloromethane (TCM), dichloroacetic acid (DCAA), trichloroacetic acid (TCAA), chlorite (ClO2(-)), and chlorate (ClO3(-)), were analyzed to observe the potential DBPs formation. Results show that US pretreatment could reduce half of ClO2 dosage compared with ClO2 disinfection alone for the same disinfection efficiency, and that an input power density of 2.64 kJ/L pretreatment with the 1.5mg/L ClO2 was enough to meet the discharge requirement in China (i.e., fecal coliform below 1000 CFU/L for Class 1A) for secondary effluent disinfection, and the ClO2(-) concentration in the disinfection effluent was only 1.37 mg/L at the same time. Furthermore, the different effects of US on the two processes (US as pretreatment and simultaneous US/ClO2 disinfection) were also analyzed, including deagglomerating, cell damage, and synergistic disinfection as well as degasing/sonolysis. It was proved that the production of TCM, DCAA, and TCAA was insignificantly influenced with the introduction of US, but US pretreatment did reduce the production of ClO2(-) and ClO3(-) effectually. In general, US pretreatment could be a better option for

  9. Role of Heparan Sulfate in Cellular Infection of Integrin-Binding Coxsackievirus A9 and Human Parechovirus 1 Isolates.

    Science.gov (United States)

    Merilahti, Pirjo; Karelehto, Eveliina; Susi, Petri

    2016-01-01

    Heparan sulfate/heparin class of proteoglycans (HSPG) have been shown to function in cellular attachment and infection of numerous viruses including picornaviruses. Coxsackievirus A9 (CV-A9) and human parechovirus 1 (HPeV-1) are integrin-binding members in the family Picornaviridae. CV-A9 Griggs and HPeV-1 Harris (prototype) strains have been reported not to bind to heparin, but it was recently shown that some CV-A9 isolates interact with heparin in vitro via VP1 protein with a specific T132R/K mutation. We found that the infectivity of both CV-A9 Griggs and HPeV-1 Harris was reduced by sodium chlorate and heparinase suggestive of HSPG interactions. We analyzed the T132 site in fifty-four (54) CV-A9 clinical isolates and found that only one of them possessed T132/R mutation while the other nine (9) had T132K. We then treated CV-A9 Griggs and HPeV-1 Harris and eight CV-A9 and six HPeV-1 clinical isolates with heparin and protamine. Although infectivity of Griggs strain was slightly reduced (by 25%), heparin treatment did not affect the infectivity of the CV-A9 isolates that do not possess the T132R/K mutation, which is in line with the previous findings. Some of the HPeV-1 isolates were also affected by heparin treatment, which suggested that there may be a specific heparin binding site in HPeV-1. In contrast, protamine (a specific inhibitor of heparin) completely inhibited the infection of both prototypes and clinical CV-A9 and HPeV-1 isolates. We conclude that T132R/K mutation has a role in heparin binding of CV-A9, but we also show data, which suggest that there are other HSPG binding sites in CV-A9. In all, we suggest that HSPGs play a general role in both CV-A9 and HPeV-1 infections.

  10. Role of Heparan Sulfate in Cellular Infection of Integrin-Binding Coxsackievirus A9 and Human Parechovirus 1 Isolates.

    Directory of Open Access Journals (Sweden)

    Pirjo Merilahti

    Full Text Available Heparan sulfate/heparin class of proteoglycans (HSPG have been shown to function in cellular attachment and infection of numerous viruses including picornaviruses. Coxsackievirus A9 (CV-A9 and human parechovirus 1 (HPeV-1 are integrin-binding members in the family Picornaviridae. CV-A9 Griggs and HPeV-1 Harris (prototype strains have been reported not to bind to heparin, but it was recently shown that some CV-A9 isolates interact with heparin in vitro via VP1 protein with a specific T132R/K mutation. We found that the infectivity of both CV-A9 Griggs and HPeV-1 Harris was reduced by sodium chlorate and heparinase suggestive of HSPG interactions. We analyzed the T132 site in fifty-four (54 CV-A9 clinical isolates and found that only one of them possessed T132/R mutation while the other nine (9 had T132K. We then treated CV-A9 Griggs and HPeV-1 Harris and eight CV-A9 and six HPeV-1 clinical isolates with heparin and protamine. Although infectivity of Griggs strain was slightly reduced (by 25%, heparin treatment did not affect the infectivity of the CV-A9 isolates that do not possess the T132R/K mutation, which is in line with the previous findings. Some of the HPeV-1 isolates were also affected by heparin treatment, which suggested that there may be a specific heparin binding site in HPeV-1. In contrast, protamine (a specific inhibitor of heparin completely inhibited the infection of both prototypes and clinical CV-A9 and HPeV-1 isolates. We conclude that T132R/K mutation has a role in heparin binding of CV-A9, but we also show data, which suggest that there are other HSPG binding sites in CV-A9. In all, we suggest that HSPGs play a general role in both CV-A9 and HPeV-1 infections.

  11. The effectiveness of selected feed and water additives for reducing Salmonella spp. of public health importance in broiler chickens: a systematic review, meta-analysis, and meta-regression approach.

    Science.gov (United States)

    Totton, Sarah C; Farrar, Ashley M; Wilkins, Wendy; Bucher, Oliver; Waddell, Lisa A; Wilhelm, Barbara J; McEwen, Scott A; Rajić, Andrijana

    2012-10-01

    Eating inappropriately prepared poultry meat is a major cause of foodborne salmonellosis. Our objectives were to determine the efficacy of feed and water additives (other than competitive exclusion and antimicrobials) on reducing Salmonella prevalence or concentration in broiler chickens using systematic review-meta-analysis and to explore sources of heterogeneity found in the meta-analysis through meta-regression. Six electronic databases were searched (Current Contents (1999-2009), Agricola (1924-2009), MEDLINE (1860-2009), Scopus (1960-2009), Centre for Agricultural Bioscience (CAB) (1913-2009), and CAB Global Health (1971-2009)), five topic experts were contacted, and the bibliographies of review articles and a topic-relevant textbook were manually searched to identify all relevant research. Study inclusion criteria comprised: English-language primary research investigating the effects of feed and water additives on the Salmonella prevalence or concentration in broiler chickens. Data extraction and study methodological assessment were conducted by two reviewers independently using pretested forms. Seventy challenge studies (n=910 unique treatment-control comparisons), seven controlled studies (n=154), and one quasi-experiment (n=1) met the inclusion criteria. Compared to an assumed control group prevalence of 44 of 1000 broilers, random-effects meta-analysis indicated that the Salmonella cecal colonization in groups with prebiotics (fructooligosaccharide, lactose, whey, dried milk, lactulose, lactosucrose, sucrose, maltose, mannanoligosaccharide) added to feed or water was 15 out of 1000 broilers; with lactose added to feed or water it was 10 out of 1000 broilers; with experimental chlorate product (ECP) added to feed or water it was 21 out of 1000. For ECP the concentration of Salmonella in the ceca was decreased by 0.61 log(10)cfu/g in the treated group compared to the control group. Significant heterogeneity (Cochran's Q-statistic p≤0.10) was observed

  12. Chloroxyanion Residue Quantification in Cantaloupes Treated with Chlorine Dioxide Gas.

    Science.gov (United States)

    Kaur, Simran; Smith, David J; Morgan, Mark T

    2015-09-01

    Previous studies show that treatment of cantaloupes with chlorine dioxide (ClO2) gas at 5 mg/liter for 10 min results in a significant reduction (P color, and a 4.6- and 4.3-log reduction of Escherichia coli O157:H7 and Listeria monocytogenes, respectively. However, this treatment could result in the presence of chloroxyanion residues, such as chloride (Cl(-)), chlorite (ClO2(-)), chlorate (ClO3(-)), and perchlorate (ClO4(-)), which, apart from chloride, are a toxicity concern. Radiolabeled chlorine dioxide ((36)ClO2) gas was used to describe the identity and distribution of chloroxyanion residues in or on cantaloupe subsequent to fumigation with ClO2 gas at a mean concentration of 5.1 ± 0.7 mg/liter for 10 min. Each treated cantaloupe was separated into rind, flesh, and mixed (rind and flesh) sections, which were blended and centrifuged to give the corresponding sera fractions. Radioactivity detected, ratio of radioactivity to mass of chlorite in initial ClO2 gas generation reaction, and distribution of chloroxyanions in serum samples were used to calculate residue concentrations in flesh, rind, and mixed samples. Anions detected on the cantaloupe were Cl(-) (∼ 90%) and ClO3(-) (∼ 10%), located primarily in the rind (19.3 ± 8.0 μg of Cl(-)/g of rind and 4.8 ± 2.3 μg of ClO3(-)/g of rind, n = 6). Cantaloupe flesh (∼ 200 g) directly exposed to(36)ClO2 gas treatment showed the presence of only Cl(-) residues (8.1 ± 1.0 μg of Cl(-)/g of flesh, n = 3). Results indicate chloroxyanion residues Cl(-) and ClO3(-) are only present on the rind of whole cantaloupes treated with ClO2 gas. However during cutting, residues may be transferred to the fruit flesh. Because Cl(-) is not toxic, only ClO3(-) would be a toxicity concern, but the levels transferred from rind to flesh are very low. In the case of fruit flesh directly exposed to ClO2 gas, only nontoxic Cl(-) was detected. This indicates that ClO2 gas that comes into contact with edible flesh would not pose a

  13. 复杂银铜精矿的沸腾焙烧综合回收工艺%Fluidized roasting synthetic reclaiming of complex silver copper concentrate

    Institute of Scientific and Technical Information of China (English)

    徐斌; 王成彦; 王忠; 赵海

    2011-01-01

    The treatment of Gacun complex silver copper concentrate with high Pb, Zn, Ag and Sb by a fluidized roasting synthetic reclaiming process was studied. The process consists of desulfurization by roasting, two-stage countercurrent leaching of copper and zinc with sulfuric acid, leaching of antimony and silver with chloride, leaching of gold with sodium chlorate, and transformation of lead with ammonia bicarbonate, and it can reclaim synthetically valuable elements well. Agglomerating of the concentrate can be avoided through controlling air surplus coefficient to be only 1.1, linear velocity in the hearth to be 0. 25 to 0. 35 m·s-1 and roasting temperature to be 600 to 630 ℃. The desulfurization ratio was 49.68% and the concentration of SO2 in smoke reached 5.5% , which meet the requirement of producing sulfuric acid in commercial production at these operating parameters.%采用沸腾焙烧综合回收工艺对呷村复杂银铜精矿难浸出问题进行实验,以沸腾焙烧脱硫、脱砷→硫酸浸出铜、锌→氯盐浸出锑、银→NaClO3氧化浸金→碳铵转化铅的工艺进行处理,实现铜、锌、银、锑、铅、金、砷和硫等有价元素的综合回收.在硫酸化沸腾焙烧过程中控制1.1倍空气过剩系数、0.25~0.35m·s-1的工况炉膛线速度以及600~630℃的焙烧温度,可以避免高铅复杂银铜精矿的烧结,脱硫率为49.68%,烟气中SO2体积分数为5.5%可满足制酸要求.

  14. Process for combined control of mercury and nitric oxide.

    Energy Technology Data Exchange (ETDEWEB)

    Livengood, C. D.; Mendelsohn, M. H.

    1999-11-03

    Continuing concern about the effects of mercury in the environment may lead to requirements for the control of mercury emissions from coal-fired power plants. If such controls are mandated, the use of existing flue-gas cleanup systems, such as wet scrubbers currently employed for flue-gas desulfurization, would be desirable, Such scrubbers have been shown to be effective for capturing oxidized forms of mercury, but cannot capture the very insoluble elemental mercury (Hg{sup 0}) that can form a significant fraction of the total emissions. At Argonne National Laboratory, we have proposed and tested a concept for enhancing removal of Hg{sup 0}, as well as nitric oxide, through introduction of an oxidizing agent into the flue gas upstream of a scrubber, which readily absorbs the soluble reaction products. Recently, we developed a new method for introducing the oxidizing agent into the flue-gas stream that dramatically improved reactant utilization. The oxidizing agent employed was NOXSORB{trademark}, which is a commercial product containing chloric acid and sodium chlorate. When a dilute solution of this agent was introduced into a gas stream containing Hg{sup 0} and other typical flue-gas species at 300 F, we found that about 100% of the mercury was removed from the gas phase and recovered in process liquids. At the same time, approximately 80% of the nitric oxide was removed. The effect of sulfur dioxide on this process was also investigated and the results showed that it slightly decreased the amount of Hg{sup 0} oxidized while appearing to increase the removal of nitric oxide from the gas phase. We are currently testing the effects of variations in NOXSORB{trademark} concentration, sulfur dioxide concentration, nitric oxide concentration, and reaction time (residence time). Preliminary economic projections based on the results to date indicate that the chemical cost for nitric oxide oxidation could be less than $5,000/ton removed, while for Hg{sup 0} oxidation it

  15. The Effects of Endogenous Mycorrhiza (Glomus spp. on Stand Establishment Rate and Yield of Open Field Tomato Crop

    Directory of Open Access Journals (Sweden)

    ANGJELINA VUKSANI

    2015-03-01

    Full Text Available Graded seeds of a tomato commercial cultivar (Suta F1 were sown in plugged (30 cm3 foam trays filled with vermiculate. For the half of seeds the substrate was homogenously mixed (10% vol/vol with broken expanded clay biologically activated by immobilized propagules of naturally occurring AM-fungi (Glomus intradadices, Glomus etunicatum, Glomus mosseae, Glomus geosporum, Glomus clarum, supplied by BioSym B.V. For the next half, it was homogenously mixed with free clay particles of the same size with the previous one (10% vol/vol. Thirty days after sowing, tomato seedlings were transplanted in to 200 cm3 plastic pots filled with vermiculite. Either AMF non pre inoculated seedlings (non AMF, or AMF pre inoculated (AMF, were equally divided in three subgroups based on the level of salinity applied in the nutrient solution (0, 50 and 100 mM sodium chlorate. On the day of transplanting and 7 days after transplanting, 10 plants were randomly selected for each experimental plot. For each of them, the dry weight of root (RW, leaf (LA, steam (SW and the whole plant (W was determined and based on that, the relative growth rates (RGR and root relative growth rate (RRGR were calculated and used as the parameters assessing the stand establishment rate of tomato seedlings after transplanting. Additionally, stomata conductance and leaf temperature were measured to assess AMF effects on physiological performance of transplanted seedlings. In order to assess the effect of AM fungi pre inoculation on total yield, parallel with pot transplanting, a field experiment was conducted according to a three replication randomized block design. It was proved that the production of open field tomato can be enhanced by the pre inoculation of AM fungi to tomato transplants at the nursery stage. Due to the pre inoculation of AM fungi, the tomato seedlings can subsequently benefit a faster stand establishment rate and higher vigor which is further reflected to a prolonged

  16. 污水处理厂反硝化除磷研究及实践%Study and application of denitrifying phosphorus removal in wastewater treatment plant

    Institute of Scientific and Technical Information of China (English)

    吴魏刚

    2011-01-01

    结合苏州娄江污水处理厂生产运行实践,研究了改良型一体化交替反应池在实现良好反硝化除磷条件下的运行工况.实践表明,提高反硝化除磷的关键是要有充足的硝酸盐氮为反硝化聚磷菌(DPB)提供电子受体,当NO-2N浓度在5 mg/L以上时,可以实现较好的反硝化除磷;当SRT为12~14 d时,反硝化除磷和系统脱氮除磷效果最好,生物除磷运行成本较低.此外,进水COD/TP、好氧池DO、厌氧池MLSS以及SRT也是影响一体化反应池生物除磷的主要因素.针对雨季低负荷运行除磷效果不理想的现象,提出了相应的工况运行措施.%Based on the practical operation of the Suzhou Loujiang Wastewater Treatment Plant, the operating condition of improved all-in-one alternate reaction tank in well denitrifying phosphorus removing condition was studied. The practice results showed: the key points to improve denitrifying phosphorus removal lied in offering enough chlorate as electron acceptor for denitrifying phosphorus bacteria (DPB); when the NO3--N concentration was above 5 mg/L, relatively good denitrifying phosphorus removal could be achieved. The best denitrifying phosphorus removal and system nitrogen and phosphorus removal could be achieved when SRT was 12~ 14 days, and the bio-phosphorus removal operation cost was low. The results also showed that influent COD/TP ratio,aerobic reaction tank DO, anaerobic tank MLSS and SRT were also main factors on all-in-one reaction tank bio-phosphorus removal effects. According to the unsatisfying low-loading phosphorus removal effects in rainy season, relating operation measures were also brought forward.

  17. Determination of Tungsten and Molybdenum in Geochemical Exploration Samples by Polarography%催化波极谱法测定化探样品中钨量及钼量

    Institute of Scientific and Technical Information of China (English)

    许卓; 于健; 马建学

    2012-01-01

    试样经碱熔分解,水提取,铁、锰、铺、镍元素量氢氧化物沉淀与钨、钼分离。在0.34moL/L硫酸-2g/L苯羟乙酸-24g/L氯酸钠-0.08g/L辛兜宁体系中,钨和锢均能产生灵敏的极谱催化波,峰电位约为-0.70V和-0.07V(对饱和日‘汞电极)。方法检出限为WO.29蚓g、Mo0.26μg/g,精密度(RSD,n=12)为W1.21%-10.1%、Mo2.7%~12.4%,准确度(RE,n=12)为W-3.7%-2.33%、Mo-4.79%~3.17%。适用于化探样品中钨钿厄索的连续测定。%The sample was melted with potassium hydroxide and extracted with water. Tungsten and molybdenum were separated from iron, manganese, cobalt and nickel with their hydroxides. In 0.34 moL/L sulfuric acid-2 g/L hydroxyphenylacetic acid-24 g/L sodium chlorate -0.08 g/L cinchonine system, tungsten and molybdenum were produced sensitive polarographic catalytic waves with peak potentials (with a saturated calomel electrode) at -0.70 V and-0.07 V, respectively. The detection limit of tungsten and molybdenum were 0.29/ag/g and 0.26μg/g, respectively. The RSD (n=12) of method were 1.21%-10.1% for W, 2.7 %~12.4 % for Mo. The RE (n=12) of method were -3.7 %-2.33 % for W,-4.79 %-3.17% for Mo. The method has been applied to the continuous determination of tungsten and molybdenum in geochemical exploration samples.

  18. Primary retention following nuclear recoil in β-decay: Proposed synthesis of a metastable rare gas oxide ((38)ArO4) from ((38)ClO4(-)) and the evolution of chemical bonding over the nuclear transmutation reaction path.

    Science.gov (United States)

    Timm, Matthew J; Matta, Chérif F

    2014-12-01

    Argon tetroxide (ArO4) is the last member of the N=50 e(-) isoelectronic and isosteric series of ions: SiO4(4-), PO4(3-), SO4(2-), and ClO4(-). A high level computational study demonstrated that while ArO4 is kinetically stable it has a considerable positive enthalpy of formation (of ~298kcal/mol) (Lindh et al., 1999. J. Phys. Chem. A 103, pp. 8295-8302) confirming earlier predictions by Pyykkö (1990. Phys. Scr. 33, pp. 52-53). ArO4 can be expected to be difficult to synthesize by traditional chemistry due to its metastability and has not yet been synthesized at the time of writing. A computational investigation of the changes in the chemical bonding of chlorate (ClO4(-)) when the central chlorine atom undergoes a nuclear transmutation from the unstable artificial chlorine isotope (38)Cl to the stable rare argon isotope (38)Ar through β-decay, hence potentially leading to the formation of ArO4, is reported. A mathematical model is presented that allows for the prediction of yields following the recoil of a nucleus upon ejecting a β-electron. It is demonstrated that below a critical angle between the ejected β-electron and that of the accompanying antineutrino their respective linear momentums can cancel to such an extent as imparting a recoil to the daughter atom insufficient for breaking the Ar-O bond. As a result, a primary retention yield of ~1% of ArO4 is predicted following the nuclear disintegration. The study is conducted at the quadratic configuration interaction with single and double excitations [QCISD/6-311+G(3df)] level of theory followed by an analysis of the electron density by the quantum theory of atoms in molecules (QTAIM). Crossed potential energy surfaces (PES) were used to construct a PES from the metastable ArO4 ground singlet state to the Ar-O bond dissociation product ArO3+O((3)P) from which the predicted barrier to dissociation is ca. 22kcal/mol and the exothermic reaction energy is ca. 28kcal/mol [(U)MP2/6-311+G(d)].

  19. The application of the atmosphere control technology for the manned submersible Jiaolong%大气环境控制技术在“蛟龙”号载人潜水器上的应用

    Institute of Scientific and Technical Information of China (English)

    姜磊; 金凤来; 侯德永; 刘帅

    2014-01-01

    介绍各种类型水下运载器如潜艇、载人深潜器等对载人密闭舱室内大气环境控制的共性要求。针对“蛟龙”号的客观条件,从动力、空间大小、浓度要求等方面分析其对大气环境控制的特殊要求。分析常见的几种密闭环境供氧及二氧化碳吸收技术如物理供氧、电解水、氧烛、超氧化物、一乙醇胺、固态胺、分子筛、碱石灰、氢氧化锂等技术各自的优缺点。在此基础上研制出一套环境控制样机,并将样机随“蛟龙”号载人潜水器进行1000,3000,5000及7000米级海试。海试的圆满成功进一步证实了样机的有效性。%Inthispapersamerequirementsoftheatmospherecontroltechnologyintheclosedspace at various underwater vehicles, such as submarine and manned submersible, are introduced. Based on the objective conditions of Jiaolong, this paper analyzed the particular demand for the atmosphere control technology from the aspects of power, space size and gases concentration. Several O2 supplying methods and CO2 absorption methods in closed space such as peroxide, physical oxygen supply, water electroanalysis, the potassium chlorate pyrogenation, mono ethanol amine( MEA) , molecular sieve, solid amine, soda lime and lithium hydroxide are compared. Based on these methods, a suitable atmosphere control technology and a prototype is developed, and the prototype is set up in the cabin of“Jiaolong” . A series of experiments has been achieved in both the South China Sea and the North-East Pacific. The validity of the prototype is approved by these experiments.

  20. 含不同氧化剂的复合推进剂能量及特征信号研究%Energetic Characteristics and Signature of Composite Propellant Containing Different Oxidizer

    Institute of Scientific and Technical Information of China (English)

    李猛; 赵凤起; 徐司雨; 姚二岗; 郝海霞; 李鑫

    2013-01-01

    为研究含能氧化剂环三亚甲基三硝胺(RDX)、六硝基六氮杂异戊兹烷(CL-20)、二硝酰胺铵(ADN)、硝仿肼(HNF)逐步取代高氯酸铵(AP)后复合推进剂的能量特性和特征信号性能,采用最小自由能原理对配方进行了化学平衡性能计算.结果表明:四种高能氧化剂逐步取代AP都达到了增加标准理论比冲和降低二次烟的目的,标准理论比冲增加率的峰值分别为0.85%,1.1%,3.37%及5.1%,ADN对降低特征信号二次燃烧火焰效果最好.ADN和HNF逐步取代A1后,标准理论比冲、一次烟及二次燃烧火焰都呈下降趋势,二次烟呈上涨趋势.%To study energetic characteristics and signature of composite propellant of Ammonium Per chlorate (AP) using a substitute of oxidant,such as Cyclotrimethylenetrinitriamine (RDX),hexanitro hexazaisowurtzitane(CL-20),Ammonium dinitramide (ADN) and Hydrazinenitroform (HNF),theoretical performance of the propellant was calculated based on the principle of free-energy minimization.The results show that theoretical specific impulse of the composite propellant is increased and signature of secondary smokes is reduced,and the most increasing rate of theoretical specific impulse are O.85%,1.1%,3.37% and 5.1%,respectively.Effects of secondary combustion of the composite propellant of AP using a substitute of ADN are decreased obviously.The energy properties are consistent with signature when the composite propellant of A1 is using a substitute of ADN and HNF.Theoretical specific impulse,primary smoke and secondary combustion of the composite propellant are all decreased.

  1. Influence of different disinfecting modes on disinfection efficiency of outlet water from sand filter%不同的消毒方式对砂滤池出水消毒效果的影响

    Institute of Scientific and Technical Information of China (English)

    李芳; 陆少鸣

    2013-01-01

    Using pilot test with the mid-positioning O3-biological activated carbon filter,influences of different disinfection methods on disinfection efficiency of outlet water from sand filter were researched by the detection and analysis of microorganism,micro aquatic animals,DBPs and AOC.The results showed that the effect of chlorine disinfection was slightly weaker than ozone disinfection combined chlorination in removing microorganisms and micro aquatic animals.For the disinfection by-production of halogenated hydrocarbon and chlorate,chlorine disinfection produced more than ozone disinfection combined chlorination,the bromated is on the same level,while the formaldehyde is the opposite.The average AOC of sand filter effluent with chlorination and with ozone disinfection combined chlorination is 75.93 μg acetic acid carbon/L and 101.23 μg acetic acid carbon/L,respectively.The latter is more than 100 μg acetic acid carbon/L,which is unbeneficial for the biology stability of water distribution system.%采用中置O3-BAC工艺进行中试实验,通过对微生物、微型生物、消毒副产物和AOC进行检测分析,研究了不同的消毒方式对砂滤池出水消毒效果的影响.结果表明,氯消毒对微型生物、微生物的去除效果稍弱于臭氧联合氯消毒;对于消毒副产物而言,氯消毒产生的卤代烃、氯酸盐的含量高于臭氧联合氯消毒,产生的溴酸盐两者处于同一水平,而产生的甲醛则是氯消毒低于臭氧联合氯消毒;氯消毒最终砂滤池出水AOC平均含量75.93 μg乙酸碳/L,臭氧联合氯消毒为101.23μg乙酸碳/L,大于100 μg乙酸碳/L,不利于供水管网的生物稳定性.

  2. Nitrification and growth of autotrophic nitrifying bacteria and Thaumarchaeota in the coastal North Sea

    Science.gov (United States)

    Veuger, B.; Pitcher, A.; Schouten, S.; Sinninghe Damsté, J. S.; Middelburg, J. J.

    2013-03-01

    Nitrification and the associated growth of autotrophic nitrifiers, as well as the contributions of bacteria and Thaumarchaeota to total autotrophic C-fixation by nitrifiers were investigated in the Dutch coastal North Sea from October 2007 to March 2008. Rates of nitrification were determined by incubation of water samples with 15N-ammonium and growth of autotrophic nitrifiers was measured by incubation with 13C-DIC (dissolved inorganic carbon) in the presence and absence of nitrification inhibitors (nitrapyrin and chlorate) in combination with compound-specific stable isotope (13C) analysis of bacterial and Thaumarchaeotal lipid biomarkers. Net nitrification during the sampling period was evident from the concentration dynamics of ammonium, nitrite and nitrate. Measured nitrification rates were high (41-221 nmol N L-1 h-1). Ammonium assimilation was always substantially lower than nitrification - with nitrification on average contributing 89% (range 73-97%) to total ammonium consumption. 13C-DIC fixation into bacterial and Thaumarchaeotal lipids was strongly reduced by the nitrification inhibitors (27-95 %). The inhibitor-sensitive 13C-PLFA (phospholipid-derived fatty acid) pool was dominated by the common PLFAs 16:0, 16:1ω7c and 18:1ω7c throughout the whole sampling period and occasionally also included the polyunsaturated fatty acids 18:2ω6c and 18:3ω3. 13C-DIC fixation activity of the nitrifying bacteria was much higher than that of the nitrifying Thaumarchaeota throughout the whole sampling period, even during the peak in Thaumarchaeotal abundance and activity. This suggests that the contribution of autotrophic Thaumarchaeota to nitrification during winter in the coastal North Sea may have been smaller than expected from their gene abundance (16S rRNA and amoA (ammonia monooxygenase)). These results emphasize the importance of direct measurements of the actual activity of bacteria and Thaumarchaeota, rather than abundance measurements only, in order to

  3. Possible Detection of Perchlorates by the Sample Analysis at Mars (SAM) Instrument: Comparison with Previous Missions

    Science.gov (United States)

    Navarro-Gonzalex, Rafael; Sutter, Brad; Archer, Doug; Ming, Doug; Eigenbrode, Jennifer; Franz, Heather; Glavin, Daniel; McAdam, Amy; Stern, Jennifer; McKay, Christopher; Coll, Patrice; Cabane, Michel; Mahaffy, Paul; Conrad, Pamela; Martin-Torres, Francisco; Zorzano-Mier, Maria; Grotzinger, John

    2013-01-01

    The first chemical analysis of soluble salts in the soil was carried out by the Phoenix Lander in the Martian Arctic [1]. Surprisingly, chlorine was present as magnesium or calcium perchlorate at 0.4 to 0.6 percent. Additional support for the identification of perchlorate came from the evolved gas analysis which detected the release of molecular oxygen at 350-550C [1]. When Mars-like soils from the Atacama Desert were spiked with magnesium perchlorate (1 percent) and heated using the Viking GC-MS protocol, nearly all the organics were combusted but a small amount was chlorinated, forming chloromethane and dichloromethane [2]. These chlorohydrocarbons were detected by the Viking GC-MS experiments when the Martian soil was analyzed but they were considered to be terrestrial contaminants [3]. Reinterpretation of the Viking results suggests <0.1 percent perchlorate and ppm levels of organic carbon at landing site 1 and 2 [2]. The suggestion of perchlorate in the Viking sites [2] has been challenged on the grounds that the detected compounds (CH3Cl and CH2Cl2) were carried from Earth [4]. Recently the Sample Analysis at Mars (SAM) instrument on board the Mars Science Laboratory (MSL) ran four samples from an aeolian bedform named Rocknest. The samples analyzed were portioned from the fifth scoop at this location. The samples were heated to 835C at 35C/min with a He flow. The SAM QMS detected a major oxygen release (300-500C) [5], coupled with the release of chlorinated hydrocarbons (chloromethane, dichloromethane, trichloromethane, and chloromethylpropene) detected both by SAM QMS and GC-MS derived from known Earth organic contaminants in the instrument [6]. Calcium perchlorate appears to be the best candidate for evolved O2 in the Rocknest samples at this time but other Cl species (e.g., chlorates) are possible and must be evaluated. The potential detection of perchlorates in Rocknest material adds weight to the argument that both Viking Landers measured signatures of

  4. Hydrogeology, degradation of ground-water quality, and simulation of infiltration from the Delaware River into the Potomac aquifers, northern Delaware

    Science.gov (United States)

    Phillips, S.W.

    1987-01-01

    Brackish water is infiltrating from the Delaware River into the underlying Potomac aquifers in the Cretaceous Potomac Formation in northern Delaware. Evidence that infiltration at the river is actually occurring includes chloride concentrations in the aquifers that are above ambient levels and chemical characteristics of groundwater and river water that are similar. Water quality within the Potomac aquifers has been degraded by the infiltration of river water and by leachate from waste disposal sites. The ambient groundwater has chloride concentrations from 10 to 21 mg/L. Chemical analyses indicate that the ambient groundwater is a sodium magnesium calcium-chloride sulfate bicarbonate type. Areas of the Potomac aquifers that have been degraded have chloride concentrations from 40 to 8,600 m/L, with specific conductances of 200 to 27 ,200 microsiemens/cm at 25 C. Chemical analyses indicate the groundwater in these areas is a sodium-chlorate type. Two wells in the lower Potomac aquifer near the Wilmington Marine Terminal also have been affected by the infiltration of river water. Leachate from waste disposal sites has caused localized groundwater degradation in all three Potomac aquifers, especially north of the Delaware Memorial Bridge and at sites near Army Creek and Red Lion Creek. Chloride concentrations up to 8,600 mg/L have resulted from waste disposal leachate. Simulated infiltration of river water into the Potomac aquifers accounts for approximately 6 to 12% of the total aquifer recharge in the area of influence of the pumping. There is a direct correlation between the rate of infiltration of river water and the total well-field pumpage. The rate of infiltration of river water for the pumping scenarios ranged from 0.31 to 0.62 million gal/day. Simulations of freshwater injection demonstrated that 12 barriers wells, each injecting 300 gal/min, would be needed to create a barrier against the infiltration of river water in the upper Potomac aquifer, whereas the

  5. High-Temperature, Perhaps Silicic, Volcanism on Mars Evidenced by Tridymite Detection in High-SiO2 Sedimentary Rock at Gale Crater, Mars

    Science.gov (United States)

    Morris, R. V.; Vaniman, D. T.; Blake, D. F.; Gellert, R.; Chipera, S. J.; Rampe, E. B.; Ming, D. W.; Morrison, S. M.; Downs, R. T.; Treiman, A. H.; Yen, A. S.; Achilles, C. N.; Bristow, T. F.; Crisp, J. A.; Des Marais, D. J.; Farmer, J. D.; Fendrich, K. V.; Frydenvang, J.; Graff, T. G.; Grotzinger, J. P.; Morookian, J. M.; Schwenzer, S. P.

    2016-01-01

    stoichiometry. The XRD-calculated amorphous component was 50 +/- 15 wt%. We constrained the value to 60 wt% because it is the minimum value necessary to give a positive Al2O3 concentration for the amorphous component using APXS data for the post-sieve dump pile (Table 2). The amorphous component has high SiO2 (approx.77 wt%) and high anion (SO3+P2O5+Cl 10 wt%) concentrations. Calculation shows that a cation-anion balance is achieved if the cations in the amorphous component except SiO2 and TiO2, which do not readily form salts, are assumed to be present as amorphous mixed-cation sulfates, phosphates, and chlorides (or perchlorates/ chlorates).

  6. Influence of specific anions on the orientational ordering of thermotropic liquid crystals at aqueous interfaces.

    Science.gov (United States)

    Carlton, Rebecca J; Ma, C Derek; Gupta, Jugal K; Abbott, Nicholas L

    2012-09-01

    We report that specific anions (of sodium salts) added to aqueous phases at molar concentrations can trigger rapid, orientational ordering transitions in water-immiscible, thermotropic liquid crystals (LCs; e.g., nematic phase of 4'-pentyl-4-cyanobiphenyl, 5CB) contacting the aqueous phases. Anions classified as chaotropic, specifically iodide, perchlorate, and thiocyanate, cause 5CB to undergo continuous, concentration-dependent transitions from planar to homeotropic (perpendicular) orientations at LC-aqueous interfaces within 20 s of addition of the anions. In contrast, anions classified as relatively more kosmotropic in nature (fluoride, sulfate, phosphate, acetate, chloride, nitrate, bromide, and chlorate) do not perturb the LC orientation from that observed without added salts (i.e., planar orientation). Surface pressure-area isotherms of Langmuir films of 5CB supported on aqueous salt solutions reveal ion-specific effects ranking in a manner similar to the LC ordering transitions. Specifically, chaotropic salts stabilized monolayers of 5CB to higher surface pressures and areal densities (12.6 mN/m at 27 Å(2)/molecule for NaClO(4)) and thus smaller molecular tilt angles (30° from the surface normal for NaClO(4)) than kosmotropic salts (5.0 mN/m at 38 Å(2)/molecule with a corresponding tilt angle of 53° for NaCl). These results and others reported herein suggest that anion-specific interactions with 5CB monolayers lead to bulk LC ordering transitions. Support for the proposition that these ion-specific interactions involve the nitrile group was obtained by using a second LC with nitrile groups (E7; ion-specific effects similar to 5CB were observed) and a third LC with fluorine-substituted aromatic groups (TL205; weak dipole and no ion-specific effects were measured). Finally, we also establish that anion-induced orientational transitions in micrometer-thick LC films involve a change in the easy axis of the LC. Overall, these results provide new insights

  7. Primary retention following nuclear recoil in β-decay: Proposed synthesis of a metastable rare gas oxide (38ArO4) from (38ClO4−) and the evolution of chemical bonding over the nuclear transmutation reaction path

    International Nuclear Information System (INIS)

    Argon tetroxide (ArO4) is the last member of the N=50 e– isoelectronic and isosteric series of ions: SiO44−, PO43−, SO42−, and ClO4−. A high level computational study demonstrated that while ArO4 is kinetically stable it has a considerable positive enthalpy of formation (of ∼298 kcal/mol) (Lindh et al., 1999. J. Phys. Chem. A 103, pp. 8295–8302) confirming earlier predictions by Pyykkö (1990. Phys. Scr. 33, pp. 52–53). ArO4 can be expected to be difficult to synthesize by traditional chemistry due to its metastability and has not yet been synthesized at the time of writing. A computational investigation of the changes in the chemical bonding of chlorate (ClO4−) when the central chlorine atom undergoes a nuclear transmutation from the unstable artificial chlorine isotope 38Cl to the stable rare argon isotope 38Ar through β-decay, hence potentially leading to the formation of ArO4, is reported. A mathematical model is presented that allows for the prediction of yields following the recoil of a nucleus upon ejecting a β-electron. It is demonstrated that below a critical angle between the ejected β-electron and that of the accompanying antineutrino their respective linear momentums can cancel to such an extent as imparting a recoil to the daughter atom insufficient for breaking the Ar–O bond. As a result, a primary retention yield of ∼1% of ArO4 is predicted following the nuclear disintegration. The study is conducted at the quadratic configuration interaction with single and double excitations [QCISD/6−311+G(3df)] level of theory followed by an analysis of the electron density by the quantum theory of atoms in molecules (QTAIM). Crossed potential energy surfaces (PES) were used to construct a PES from the metastable ArO4 ground singlet state to the Ar–O bond dissociation product ArO3+O(3P) from which the predicted barrier to dissociation is ca. 22 kcal/mol and the exothermic reaction energy is ca. 28 kcal/mol [(U)MP2/6–311+G

  8. Nitrification and growth of autotrophic nitrifying bacteria and Thaumarchaeota in the coastal North Sea

    Directory of Open Access Journals (Sweden)

    B. Veuger

    2012-11-01

    Full Text Available Nitrification and the associated growth of autotrophic nitrifiers, as well as the contributions of bacteria and Thaumarchaeota to total autotrophic C-fixation by nitrifiers were investigated in the Dutch coastal North Sea from October 2007 to March 2008. Rates of nitrification were determined by incubation of water samples with 15N-ammonium and growth of autotrophic nitrifiers was measured by incubation with 13C-DIC in the presence and absence of nitrification inhibitors (nitrapyrin and chlorate in combination with compound-specific stable isotope (13C analysis of bacterial- and Thaumarchaeotal lipid biomarkers. Net nitrification during the sampling period was evident from the concentration dynamics of ammonium, nitrite and nitrate. Measured nitrification rates were high (41–221 nmol N l−1h−1. Ammonium assimilation was always substantially lower than nitrification with nitrification on average contributing 89% (range 73–97% to total ammonium consumption.

    13C-DIC fixation into bacterial and Thaumarchaeotal lipids was strongly reduced by the nitrification inhibitors (27–95%. The inhibitor-sensitive 13C-PLFA pool was dominated by the common PLFAs 16:0, 16:1ω7c and 18:1ω7c throughout the whole sampling period and occasionally also included the polyunsaturated fatty acids 18:2ω6c and 18:3ω3. Cell-specific 13C-DIC fixation activity of the nitrifying bacteria was much higher than that of the nitrifying Thaumarchaeota throughout the whole sampling period, even during the peak in Thaumarchaeotal abundance and activity. This suggests that the contribution of autotrophic Thaumarchaeota to nitrification during winter in the coastal North Sea may have been smaller than expected from their gene abundance. These results emphasize the importance of direct measurements of the actual activity of bacteria and Thaumarchaeota, rather than abundance

  9. Nitrification and growth of autotrophic nitrifying bacteria and Thaumarchaeota in the coastal North Sea

    Directory of Open Access Journals (Sweden)

    B. Veuger

    2013-03-01

    Full Text Available Nitrification and the associated growth of autotrophic nitrifiers, as well as the contributions of bacteria and Thaumarchaeota to total autotrophic C-fixation by nitrifiers were investigated in the Dutch coastal North Sea from October 2007 to March 2008. Rates of nitrification were determined by incubation of water samples with 15N-ammonium and growth of autotrophic nitrifiers was measured by incubation with 13C-DIC (dissolved inorganic carbon in the presence and absence of nitrification inhibitors (nitrapyrin and chlorate in combination with compound-specific stable isotope (13C analysis of bacterial and Thaumarchaeotal lipid biomarkers. Net nitrification during the sampling period was evident from the concentration dynamics of ammonium, nitrite and nitrate. Measured nitrification rates were high (41–221 nmol N L−1 h−1. Ammonium assimilation was always substantially lower than nitrification – with nitrification on average contributing 89% (range 73–97% to total ammonium consumption. 13C-DIC fixation into bacterial and Thaumarchaeotal lipids was strongly reduced by the nitrification inhibitors (27–95 %. The inhibitor-sensitive 13C-PLFA (phospholipid-derived fatty acid pool was dominated by the common PLFAs 16:0, 16:1ω7c and 18:1ω7c throughout the whole sampling period and occasionally also included the polyunsaturated fatty acids 18:2ω6c and 18:3ω3. 13C-DIC fixation activity of the nitrifying bacteria was much higher than that of the nitrifying Thaumarchaeota throughout the whole sampling period, even during the peak in Thaumarchaeotal abundance and activity. This suggests that the contribution of autotrophic Thaumarchaeota to nitrification during winter in the coastal North Sea may have been smaller than expected from their gene abundance (16S rRNA and amoA (ammonia monooxygenase. These results emphasize the importance of direct measurements of the actual activity of bacteria and Thaumarchaeota, rather than abundance

  10. Nitrification and growth of autotrophic nitrifying bacteria and Thaumarchaeota in the coastal North Sea

    Science.gov (United States)

    Veuger, Bart; Pitcher, Angela; Schouten, Stefan; Sinninghe Damsté, Jaap S.; Middelburg, Jack J.

    2013-04-01

    A dual stable isotope (15N and 13C) tracer approach in combination with compound-specific stable isotope analysis of bacterial and Thaumarchaeotal lipid biomarkers was used to investigate nitrification and the associated growth of autotrophic nitrifiers in the Dutch coastal North Sea. This study focusses on the stoichiometry between nitrification and DIC fixation by autotrophic nitrifiers as well as on the contributions of bacteria versus Thaumarchaeota to total autotrophic DIC-fixation by nitrifiers. Water from the dutch coastal North Sea was collected at weekly to biweekly intervals during the winter of 2007-2008. Watersamples were incubated with 15N-labeled ammonium and 15N was traced into nitrate and suspended material to quantify rates of nitrification and ammonium assimilation respectively. Growth of autotrophic nitrifiers was measured by incubating water samples with 13C-DIC in the presence and absence of nitrification inhibitors (nitrapyrin and chlorate) and subsequent analysis of 13C in bacterial phospholipid-derived fatty acids (PLFAs) and the Thaumarchaeotal biomarker crenarchaeol. Results revealed high nitrification rates with nitrification being the primary sink for ammonium. 13C-DIC fixation into bacterial and Thaumarchaeotal lipids was strongly reduced by the nitrification inhibitors (27-95%). The ratio between rates of nitrification versus DIC fixation by nitrifiers was higher or even much higher than typical values for autotrophic nitrifiers, indicating that little DIC was fixed relative to the amount of energy that was generated by nitrification, and hence that other other processes for C acquisition may have been relevant as well. The inhibitor-sensitive 13C-PLFA pool was dominated by the common PLFAs 16:0, 16:1ω7c and 18:1ω7c throughout the whole sampling period and occasionally also included the polyunsaturated fatty acids 18:2ω6c and 18:3ω3. Cell-specific 13C-DIC fixation activity of the nitrifying bacteria was much higher than that of the

  11. Influence of ultrasound enhancement on chlorine dioxide consumption and disinfection by-products formation for secondary effluents disinfection.

    Science.gov (United States)

    Zhou, Xiaoqin; Zhao, Junyuan; Li, Zifu; Lan, Juanru; Li, Yajie; Yang, Xin; Wang, Dongling

    2016-01-01

    Chlorine dioxide (ClO2) has been promoted as an alternative disinfectant because of its high disinfection efficiency and less formation of organic disinfection by-products (DBPs). However, particle-associated microorganisms could be protected during the disinfection process, which decreases the disinfection efficiency or increases the required dosage. Besides, the formation of inorganic disinfection by-products is a significant concern in environment health. Ultrasound (US)-combined disinfection methods are becoming increasingly attractive because they are efficient and environmentally friendly. In this study, US was introduced as an enhancement method to identify its influence on ClO2 demand reduction and to minimize the production of potential DBPs for secondary effluents disinfection. Fecal coliform was used as an indicator, and DBPs, including trichloromethane (TCM), dichloroacetic acid (DCAA), trichloroacetic acid (TCAA), chlorite (ClO2(-)), and chlorate (ClO3(-)), were analyzed to observe the potential DBPs formation. Results show that US pretreatment could reduce half of ClO2 dosage compared with ClO2 disinfection alone for the same disinfection efficiency, and that an input power density of 2.64 kJ/L pretreatment with the 1.5mg/L ClO2 was enough to meet the discharge requirement in China (i.e., fecal coliform below 1000 CFU/L for Class 1A) for secondary effluent disinfection, and the ClO2(-) concentration in the disinfection effluent was only 1.37 mg/L at the same time. Furthermore, the different effects of US on the two processes (US as pretreatment and simultaneous US/ClO2 disinfection) were also analyzed, including deagglomerating, cell damage, and synergistic disinfection as well as degasing/sonolysis. It was proved that the production of TCM, DCAA, and TCAA was insignificantly influenced with the introduction of US, but US pretreatment did reduce the production of ClO2(-) and ClO3(-) effectually. In general, US pretreatment could be a better option for

  12. Cáncer gástrico en Costa Rica: ¿existe o no relación con la cloración del agua para consumo humano?

    Directory of Open Access Journals (Sweden)

    Darner A Mora Alvarado

    2007-07-01

    significant link between the incidence of GC and the consumption of chlorinated water in Costa Rica. The analysis used the GC-mortality results in 458 districts during the years 1999 to 2002 and the data obtained from the National Water Laboratory on the type of water (chlorinated or not, the number of years of disinfection and the source of the water (underground, surface or mixed. For the statistical analysis, a Standardized Mortality Index (IME and the Pearson correlation coefficient were used. Results showed no relationship between incidence of GC and the chloration of water for human consumption (ACH, even after taking into account the number of years of chloration and also the type of water source used (underground or superficial. Lastly, it is recommended that the Costa Rican Institute of Waters and Sewer Systems (A y A as the leading supplier of drinking water, carry out an educational campaign with the purpose of reducing the lack of user confidence in the consumption of chlorinated ACH. Besides, A y A must promote the study of the relationship of ACH with other types of cancer such as bladder and colorectal cancer.

  13. Microbial degradation of chloroethenes in groundwater systems

    Science.gov (United States)

    Bradley, Paul M.

    éthane (DCE) et le chlorure de vinyl (VC). Bien que des études de laboratoire réalisées avec des micro-organismes adaptés aux composés halogénés montrent que la réduction complète en éthane est possible, dans la plupart des nappes la réaction de déchloration par réduction s'arrête apparemment au DCE et au VC. Cependant, des recherches récentes menées sur des sédiments d'un aquifère et d'alluvions ont démontré que l'oxydation microbienne de ces descendants réduits peut se produire de manière significative dans des conditions de redox anérobies. La déchloration par réduction de PCE et de TCE dans des conditions anérobies suivie par une oxydation microbienne anérobie des DCE et VC fournit une piste microbienne possible pour obtenir une dégradation complète des chloroéthanes polluants dans les aquifères. Resumen Los cloroetanos (tetracloroetano PCE y tricloroetano TCE) son contaminantes muy habituales en los acuíferos. Hasta 1980 se consideraba que los cloroetanos no eran biodegradables y, por tanto, los métodos de rehabilitación en acuíferos contaminados con cloroetanos se limitaban al pump-and-treat, generalmente con poco éxito. Posteriormente se vio que, en condiciones reductoras, algunos microorganismos pueden reducir PCE y TCE a unos subproductos menos clorados, como el dicloroetano (DCE) y el cloruro de vinilo (VC). Aunque estudios de laboratorio recientes sugieren que la reducción completa a etano es posible, en la mayoría de los sistemas acuíferos la decloración suele detenerse en los DCE o VC. Sin embargo, investigaciones más recientes en acuíferos y sedimentos fluviales demuestran que la oxidación microbiana de estos subproductos puede ser importante bajo condiciones redox anaerobias. La combinación de la reducción de PCE y TCE en condiciones anaerobias seguida de la oxidación microbiana anaerobia de DCE y VC proporciona un método potencial para la degradación total de los cloroetanos en los sistemas acuíferos.

  14. Comparative study on precipitation methods of yellow-cake from acid leachate of rock phosphate and Its purification

    International Nuclear Information System (INIS)

    This study was carried-out to leach uranium from rock phosphate using sulphuric acid in presences of potassium chlorate as an oxidant and to investigate the relative purity of different forms of yellow cakes produced with ammonia ((NH4)2 U2 O7), magnesia (UO3.xH2O) and sodium hydroxide (Na2U2O7) as precipitants, as well as purification of the products with TBP extraction and matching its impurity levels with specification of the commercial products. Alpha-particle spectrometry was for used for determination of activity concentration of uranium isotopes (''2''3''4U and ''2''3''8U) in rock phosphate, resulting green phosphoric acid solution, and in different forms of the yellow cake from which the equivalent mass concentration of uranium was deduced. Likewise, AAS was used for determination of impurities (Pb, Ni, Cd, Fe, Zn, Mn, and Cu). On the average, the activity concentration of uranium in the rock phosphate was 1468±979 Bq/Kg (119.38±79.66 ppm), and 711±252 Bq/L (57.85±20.46 ppm) in the resulting green solution with corresponding percent of dissolution amounting to 48% which is considered low indicating that the experimental conditions (i.e. dissolution container, temperature, PH, retention time) were not optimal. However, the isotopic ratio (''2''3''4U, ''2''3''8U) in all stages of hydrometallurgical process was not much different from unity indicating lack of fractionation. Crude yellow cakes (hydrate uranium trioxide, ammonium diuranate and sodium diuranate) were precipitated from the green solutions prior to separation of iron and once after iron separation. Although, iron was tested using bipyridine and SCN, it was found in all types of crude samples analyzed this might be attributed to either the quality of the reagent used or inhibition of Fe present in the solution by stronger complexing agent. Uranium mass concentration in crude yellow cakes precipitated before iron separation was found following the order: UO3.xH2O>ammonium diuranate

  15. Development of sustainable Palladium-based catalysts for removal of persistent contaminants from drinking water

    Science.gov (United States)

    Shuai, Danmeng

    Pd-based catalytic reduction has emerged as an advanced treatment technology for drinking water decontamination, and a suite of persistent contaminants including oxyanions, N-nitrosoamines, and halogenated compounds are amenable to catalytic reduction. The primary goal of this study is to develop novel Pd-based catalysts with enhanced performance (i.e., activity, selectivity, and sustainability) to remove contaminants from drinking water. The effects of water quality (i.e., co-contaminants in water matrix), catalyst support, and catalyst metal were explored, and they provide insights for preparing catalysts with faster kinetics, higher selectivity, and extended lifetime. Azo dyes are wide-spread contaminants, and they are potentially co-exisiting with target contaminants amenable for catalytic removal. The probe azo dye methyl orange (MO) enhanced catalytic reduction kinetics of a suite of oxyanions (i.e., nitrate, nitrite, bromate, chlorate, and perchlorate) and diatrizoate significantly but not N-nitrosodimethylamine (NDMA) with a variety of Pd-based catalysts. Nitrate was selected as a probe contaminant, and several different azo dyes (i.e., (methyl orange, methyl red, fast yellow AB, metanil yellow, acid orange 7, congo red, eriochrome black T, acid red 27, acid yellow 11, and acid yellow 17) were evaluated for their ability to enhance reduction. A hydrogen atom shuttling mechanism was proposed and a kinetic model was proposed based on Bronsted-Evans-Polanyi (BEP) theory, and they suggest sorbed azo dyes and reduced hydrazo dyes shuttle hydrogen atoms to oxyanions or diatrizoate to enhance their reduction kinetics. Next, vapor-grown carbon nanofiber (CNF) supports were used to explore the effects of Pd nanoparticle size and interior versus exterior loading on nitrite reduction activity and selectivity (i.e., dinitrogen over ammonia production). In order to evaluate the amount of interior versus exterior loading of Pd nanoparticles, a fast and accurate geometric

  16. Determination of Anions in High Chloride Matrix by Ion Chromatography with Pre Online Sample Preparation Technique%谱睿在线除氯技术检测高氯水样中的阴离子

    Institute of Scientific and Technical Information of China (English)

    张夕虎; 刘肖

    2011-01-01

    We developed a method in which Dionex "Pre" online sample preparation technique was used to remove chloride by Ag cartridge and Na cartridge. This method is applicable to a wide range of samples and is simpler than offline approach. Each Ag cartridge carries on 400 consecutive injections (25 microlitre each) of 1% NaCl solution, and the removal efficiency is still above 99%. The separation of anions was carried out by high capacity hydroxide selectivity IonPac ASll-HC gradient separation column while Eluent Generator was employed to generate gradient KOH eluent online automatically. Two valves were switched to finish the injection. The system removes chloride well online for different matrix as analysis grade salt and sodium chloride. The detection limits of bromate, chlorate, chlorite, nitrite, nitrate and sulfate are less than 10μg/L, and the recoveries are between 80% and 110%. This method holds the advantages of easy-operation, good reproducibility, lower operation cost etc and is more convenient than off-line approach.%采用戴安公司谱睿(Pre)在线样品前处理技术,使用高容量在线Ag柱和Na柱,开发出了一种柱前去除高氯基体中氯离子的在线分析方法.操作简便,且适用样品范围广;不更换Ag柱可耐受10g/L NaCl基体,25μL连续进样400针,氯离子去除效率可保持在99%以上.系统选用高容量IonPac AS11-HC氢氧根体系阴离子交换色谱柱,在线淋洗液自动发生装置进行梯度淋洗,用抑制型电导检测.对食盐、分析纯氯化钠等不同基体进行检测,可实现样品在线除氯,并可检测其中不高于10μg/L的溴酸根、氯酸根、亚硝酸根、硝酸根和硫酸根等离子.不同离子校准曲线相关系数均在99.8%以上,加标回收率为80%~110%.该技术具有操作简单、可重复性强、方法新颖等特点,解决了以往高氯基体检测成本过高、适用范围有限、前处理操作复杂等问题.

  17. Research on the Oxidation Starch Preparation by Microwave Heating using New Oxidant and its Property%新型氧化剂微波干法制备氧化淀粉及其性能研究

    Institute of Scientific and Technical Information of China (English)

    彭佳莹; 周露; 杨椰; 钟耕

    2012-01-01

    Preparing modified starch by using dry method of microwave has been gradually promoted in China. It has some advantages such as short process, low energy consumption, easy to operate. The process of preparing oxidation starches by two oxidants; chlorine dioxide (to oxidation starch A) and sodium chlorate (to oxidation starch B) was investigated, and the characteristics of the modified starches were also discussed in this paper. The results on theprocess study showed that the oxidation reaction on starch could be caused by both oxidants using dry method of microwave heating. The carboxyl group content of oxidation starch A and oxidation starch B prepared by the method were (0.068 ±0.002)% and (0.586 ±0.002)% separately. The results on the properties of the modified starches showed that the thermal viscosity stability of the oxidation starch was improved and freeze - thaw stability of oxidation starch B was better. The release water rate of oxidation starch B was only 23.7% after freeze thawing twice. The alkali resistance of oxidation starch A was good, but not to the acid resistance. However, oxidation starch B showed a better alkali resistance and acid resistance. The oxidizing reaction to the modified starches happened in amorphous of the starch through X - ray diffraction. However, the crystal structure remains the same as the original starch.%干法制备变性淀粉已逐步在国内推广,它具有流程短,能耗低,操作简便等优点.采用微波干法工艺,研究了二氧化氯、氯酸钠两种氧化剂制备氧化淀粉(分别为氧化淀粉A和氧化淀粉B)的工艺和变性淀粉的性能.工艺研究表明,两种氧化剂均能通过微波干法制备氧化淀粉,而氧化淀粉A和氧化淀粉B的羧基含量分别为(0.068±0.002)%和(0.586±0.002)%.性能研究表明,氧化淀粉的热黏度稳定性得到了改善,氧化淀粉B的冻融稳定性较好,经2次冻融,析水率仅为23.7%;氧化淀粉A耐碱性能好,耐酸性较差,

  18. Destruction and Sequestration of H2O on Mars

    Science.gov (United States)

    Clark, Benton

    2016-07-01

    The availability of water in biologically useable form on any planet is a quintessential resource, even if the planet is in a zone habitable with temperature regimes required for growth of organisms (above -18 °C). Mars and most other planetary objects in the solar system do not have sufficient liquid water at their surfaces that photosynthesis or chemolithoautotrophic metabolism could occur. Given clear evidence of hydrous mineral alteration and geomorphological constructs requiring abundant supplies of liquid water in the past, the question arises whether this H2O only became trapped physically as ice, or whether there could be other, more or less accessible reservoirs that it has evolved into. Salts containing S or Cl appear to be ubiquitous on Mars, having been measured in soils by all six Mars landed missions, and detected in additional areas by orbital investigations. Volcanoes emit gaseous H2S, S, SO2, HCl and Cl2. A variety of evidence indicates the geochemical fate of these gases is to be transformed into sulfates, chlorides, chlorates and perchlorates. Depending on the gas, the net reaction causes the destruction of between one and up to eight molecules of H2O per atom of S or Cl (although hydrogen atoms are also released, they are lost relatively rapidly to atmospheric escape). Furthermore, the salt minerals formed often incorporate H2O into their crystalline structures, and can result in the sequestration of up to yet another six (sometimes, more) molecules of H2O. In addition, if the salts are microcrystalline or amorphous, they are potent adsorbents for H2O. In certain cases, they are even deliquescent under martian conditions. Finally, the high solubility of the vast majority of these salts (with notable exception of CaSO4) can result in dense brines with low water activity, aH, as well as cations which can be inimical to microbial metabolism, effectively "poisoning the well." The original geologic materials on Mars, igneous rocks, also provide some

  19. Exposure assessment of a burning ground for chemical ammunition on the Great War battlefields of Verdun.

    Science.gov (United States)

    Bausinger, Tobias; Bonnaire, Eric; Preuss, Johannes

    2007-09-01

    severe arsenic contamination and the transfer of this carcinogen by leachate, surface runoff and probably by wind. Nevertheless, some studies on the effects of the contaminant inventory on the local vegetation revealed that ammonium nitrate elutable zinc is responsible for the spatial distribution of some tolerant plant species and not arsenic. Previously undetected buried munitions from the former delaboration facility can be an other source of environmental contaminants. This is supported by elevated concentrations of chlorate (cmax.=71 mg/l) and perchlorate (cmax.=0.8 mg/l) detected in the leachate samples. This is the second report about environmental contamination related to post-war ammunition destruction activities along the 1914/18 Western Front.

  20. 二氧化氯消毒饮用水中亚氯酸盐污染的初步研究%Priliminary Study on Chlorite Pollution of Drinking Water Disinfected by Chlorine Dioxide

    Institute of Scientific and Technical Information of China (English)

    施小平; 周明浩

    2000-01-01

    [Objective] To explore the status of chlorite pollution in drinking water due to chlorine dioxide , aswell as its causes and counter measures. [Methods]A water plant collecting surface water as raw water slightly pol-luted by organic compounds and B water plant collecting ground water without organic compounds pollution wereselected as observed objectives. Chlorine dioxide generators were used in both of A and B water plants, their rawmaterials was chlorite for A plant and chlorate for B plant. The levels of chlorite in treated water from these twowater plants were determined by amperometric titration. [Results]The levels of chlorite in treated water of A waterplant ranged 0.530~0.760 mg/L, 2.6~3.8 times of the standard value, with a over standard rate of 100%, thelevels of B water plant range 0.257~0.733 mg/L, 1.3~3.7 times of the standard value, with a over standard rateof 83.3%. [Conclusion] The treated water of A and B water plants presented higher pollution by chlorite, the by-product of chlorine dioxide disinfection.%[目的]了解二氧化氯消毒饮用水产生的亚氯酸盐(ClO2-)污染现状,并探讨其成因和对策。[方法]选择2个自来水厂,其中甲水厂以受轻度有机物污染的地面水为水源,乙水厂以未受有机物污染的地下水为水源,两个水厂均使用二氧化氯发生器,主要原料甲厂为亚氯酸盐,乙厂为氯酸盐。采用电流滴定仪法测定这2个水厂出厂水中ClO2-浓度。[结果]出厂水ClO2-浓度:甲厂0.530~0.760 mg/L,为标准值的2.6~3.8倍,超标率100%;乙厂0.100~0.733 mg/L,其中超标浓度值范围0.257~0.733 mg/L,为标准值的1.3~3.7倍,超标率83.3%。[结论]甲、乙自来水厂出厂水中由二氧化氯消毒产生的消毒副产物亚氯酸盐污染较严重。

  1. Calidad físico-química y microbiólogica del agua en parques acuáticos Physicist-chemistry and Microbiological Water Quality in Aquatic Parks

    Directory of Open Access Journals (Sweden)

    Beatriz Helena Díaz-Solano

    2011-04-01

    establishments. As study zone was chosen the Morelos State, Mexico, which has four water parks. The study analyzed one of these parks, dividing the study as follow: Phase 1 Sampling of water in and out of the park, analyzing physicochemical and microbiological parameters; and Phase 2 Operational evaluation in six pools of water Park, assessing the electrical conductivity, Total Dissolved Solids (TDS, pH, color, turbidity and residual chlorine. The results were compared with Mexican Official Standards, determining whether there is deterioration in the quality of the resource in the operational processes of the parks. The Phase 1 gave as results raised levels in fats and oils (19.0 mg/L, color (100 UPt-Co, fecal coliforms (1.15 · 10(4 NMP/100 mL and total coliforms (1.70 · 10(5 NMP/100 mL. The Phase 2 showed high values of pH (7.9-8.4, diminishing the efficiency in disinfection and a behavior differentiated in conductivity and TDS in swimming pools filtering systems. Since conclusions there decided that the water quality in Water Parks must be controlled in parallel to the operability in swimming pools, the processes of chloration must be standardized. The users are responsible for the deterioration of water and require the generation of an Environmental Management System.

  2. Aspectos clínicos e características do leite em ovelhas com mastite induzida experimentalmente com Staphylococcus aureus Clinical aspects and characteristics of the milk in sheep with mastitis experimentally induced with Staphylococcus aureus

    Directory of Open Access Journals (Sweden)

    Rogério A. Santos

    2007-01-01

    and fat. The pH, the chlorates and CCS reached very high indexes, accompanied by the CMT test reaction. The bacteriological exam revealed the presence of S. aureus during the phase of infection. After the treatment of the sheep 36 hours PI, one animal came to death 48h PI, and the others showed clinical recovery; however there was no physiologic re-establishment of the inoculated udders which lost their function.

  3. Role of MMP1, MMP2 and TIMP2 in treatment of pulmonary interstitial fibrosis in rats with Xiongfufang%MMP1,MMP2和TIMP2在雄附方干预大鼠肺间质纤维化中的作用

    Institute of Scientific and Technical Information of China (English)

    王勇; 杨永滨; 马玉琛

    2013-01-01

      目的探讨基质金属蛋白酶(MMP1和MMP2)和内源性基质金属蛋白酶组织抑制因子(TIMP2)的活性变化在雄附方干预大鼠肺间质纤维化形成机制中的可能作用.方法70只SD健康大鼠随机分为对照组(BC)、假手术组(PS)、纤维化模型组(MD)、醋酸泼尼松组(PN 5.6 mg/kg)、雄附方高、中、低剂量组(XFFH、XFFM和XFFL 1.4 g/kg、0.7 g/kg、0.35 g/kg)7组,每组10只.于造模后第2天用0.9%氯化钠注射液(0.014 L/kg)或相应药物(0.014 L/kg)每天灌胃(ig),4周后取右肺中叶组织,应用免疫组织化学染色(SP)法检测肺组织中MMP1、MMP2和TIMP2的表达水平.结果 MMP1、MMP2和TIMP2在MD组阳性表达水平均为各组最高(P<0.01);用药组中XFFH组MMP1、MMP2和TIMP2的阳性表达水平均最低(P<0.01);XFFH组与BC和PS组相比TIMP2表达增强(P<0.05).结论雄附方对抗肺组织纤维化的形成机制可能与其有效平衡肺组织中MMP1、MMP2和TIMP2的表达水平有关.%Objective To study the role of MMP1, MMP2 and TIMP2 in treatment of pulmonary interstitial fibrosis in rats with Xiongfufang and its mechanism. Methods Seventy healthy SD rats were randomly divided into control group, sham operation group, fibrosis model group, prednione acetate group, and high, medium, low Xiongfufang dose groups (10 in each group). On day 2 after a model was established, the rats were given 0.9%sodium chlorate or gastric drugs for 4 weeks. Expressions of MMP1, MMP2 and TIMP2 in lung tissue were detected with SP staining. Results The expression levels of MMP1, MMP2 and TIMP2 were significantly higher in fibrosis model group than in different drug treatment groups (P<0.01). The expression level of TIMP2 was significantly higher in high Xiongfufang dose group than in control group and sham operation group (P<0.05). Conclusion Xiongfufang prevents lungs against their interstitial fibrosis possibly by regulating the expression of MMP1, MMP2, and TIMP2 in lung tissue.

  4. 利用糠醛废水生产环保融雪剂的工艺研究%Research on the Process of Producing Environmentally-friendly Snowmelt Agent with Furfural Water

    Institute of Scientific and Technical Information of China (English)

    赵国明; 于广军

    2012-01-01

    To protect environment and public facilities from damage of the pollution of furfural water and chlorate snowmelt agent, we come up with the new craft, which produce environmentally-friendly snowmelt agent-calcium magnesium acetate (CMA) from the acetic acid reaction of limestone, magnesium oxide and furfural water. First we make concentrate by double-effect evaporating neutralized furfural water, then produce calcium magnesium acetate in high concentration by adsorpting the concentrate with active carbon, and deliver the evaporated condensated water back to the furfural production, as a result the reusing of furfural water and zero discharge conies true. This article researches the process and parameters of producing environmentally-friendly snowmelt agent-calcium magnesium acetate with furfural water, which are based on experiments. The purity of the calcium magnesium acetate reached 92%, which well conforms to the quality specification of environmentally-friendly snowmelt agent. It accomplishes the efficient resources utilization of the furfural water by solving the bottleneck problem of non-environmentally-friendly producing the furfural, and lower the production cost by leaps aiid bounds. Finally the reusing of furfural water transfers from absolute investment to earning industry.%为解决目前糠醛废水产生的污染以及氯盐融雪剂对环境和公共设施造成的危害,提出采用新工艺,用石灰石、氧化镁等和糠醛塔底废水中的醋酸反应,直接制取环保型融雪剂醋酸钙镁(CMA)技术,并将中和后的废水经双效蒸发得到浓缩液,将浓缩液使用活性炭吸附得到纯度较高的醋酸钙镁,蒸发冷凝水回用糠醛生产,从而实现糠醛废水的资源化利用,达到污水的零排放.本论文通过实验研究确定利用糠醛废水生产环保融雪剂醋酸钙镁的工艺流程及参数,使生产的醋酸钙镁纯度达到92%,完全符合环保融雪剂的质量标准,既解决了制约糠醛

  5. SYNTHESIS OF SULFUR-BASED WATER TREATMENT AGENT FROM SULFUR DIOXIDE WASTE STREAMS

    Energy Technology Data Exchange (ETDEWEB)

    Robert C. Brown; Maohong Fan; Adrienne Cooper

    2004-11-01

    Absorption of sulfur dioxide from a simulated flue gas was investigated for the production of polymeric ferric sulfate (PFS), a highly effective coagulant useful in treatment of drinking water and wastewater. The reaction for PFS synthesis took place near atmospheric pressure and at temperatures of 30-80 C. SO{sub 2} removal efficiencies greater than 90% were achieved, with ferrous iron concentrations in the product less than 0.1%. A factorial analysis of the effect of temperature, oxidant dosage, SO{sub 2} concentration, and gas flow rate on SO{sub 2} removal efficiency was carried out, and statistical analyses are conducted. The solid PFS was also characterized with different methods. Characterization results have shown that PFS possesses both crystalline and non-crystalline structure. The kinetics of reactions among FeSO{sub 4} {center_dot} 7H{sub 2}O, NaHSO{sub 3} and NaClO{sub 3} was investigated. Characterizations of dry PFS synthesized from SO{sub 2} show the PFS possesses amorphous structure, which is desired for it to be a good coagulant in water and wastewater treatment. A series of lab-scale experiments were conducted to evaluate the performance of PFS synthesized from waste sulfur dioxide, ferrous sulfate and sodium chlorate. The performance assessments were based on the comparison of PFS and other conventional and new coagulants for the removal of turbidity and arsenic under different laboratory coagulant conditions. Pilot plant studies were conducted at Des Moines Water Works in Iowa and at the City of Savannah Industrial and Domestic (I&D) Water Treatment Plant in Port Wentworth, Georgia. PFS performances were compared with those of conventional coagulants. The tests in both water treatment plants have shown that PFS is, in general, comparable or better than other coagulants in removal of turbidity and organic substances. The corrosion behavior of polymeric ferric sulfate (PFS) prepared from SO{sub 2} and ferric chloride (FC) were compared. Results

  6. Efeito da cloração da água de beber e do nível energético da ração sobre o ganho de peso e consumo de água em frangos de corte Effect of drinking water chlorination and dietary energy level on body weight gain and water intake in broiler chickens

    Directory of Open Access Journals (Sweden)

    Renato Luis Furlan

    1999-01-01

    Full Text Available Dois experimentos foram realizados com o objetivo de pesquisar o efeito da adição de cloro à água de beber e dos diferentes níveis de energia na ração sobre o ganho de peso e consumo de água em frangos de corte. No experimento 1, as aves foram alimentadas com dois níveis de energia metabolizável na ração (2900 e 3200 kcal EM/kg em cada fase da criação. Foi observado que o nível energético não influi no consumo de água e no ganho de peso dos frangos de corte. No experimento 2, o nível de energia metabolizável da ração foi de 3200 kcal EM/kg e a água de beber foi clorada com hipoclorito de sódio a 11%, correspondendo a 5 ppm de cloro. O consumo de água foi menor nas aves que receberam água clorada. Apesar de o consumo de água ter sido menor, não houve redução no ganho de peso das aves que receberam hipoclorito de sódio. A adição de cloro à água de beber melhorou os índices bacteriológicos. Os resultados obtidos nestes experimentos evidenciam que os níveis energéticos das rações testadas não influenciaram o consumo de água dos frangos de corte; entretanto, a adição de cloro reduziu a ingestão de água, porém sem influir no ganho de peso nas aves tratadas.Two experiments were conducted to study the effect of adding chlorine on drinking water and different dietary energy levels on the body weight gain and water intake in broiler chickens. In Experiment 1, broilers were fed diets containing two levels of energy (2900 and 3200 kcal ME/kg in each growing phase. The dietary energy level did not affect the water intake and the body weight gain of the broilers. In experiment 2, the dietary metabolizable energy level was 3200 kcal ME/kg and drinking water was treated with sodium hypochlorine at 11% corresponding to 5 ppm of chloride. The water intake was reduced in the birds that received chlorated drinking water, however, there was no reduction on body weight gain in birds that received sodium hypochlorine

  7. Laser-induced Fluorescence Spectroscopy for applications in chemical sensing and optical refrigeration

    Science.gov (United States)

    Kumi Barimah, Eric

    Laser-induced breakdown spectroscopy (LIBS) is an innovative technique that has been used as a method for fast elemental analysis in real time. Conventional ultraviolet-visible (UV-VIS) LIBS has been applied to detect the elemental composition of different materials, including explosives, pharmaceutical drugs, and biological samples. The extension of conventional LIBS to the infrared region (˜1-12 mum) promises to provide additional information on molecular emission signatures due to rotational-vibrational transitions. In this research, a pulsed Nd: YAG laser operating at 1064 nm was focused onto several sodium compounds (NaCl, NaClO3, Na2CO3 and NaClO4) and potassium compounds (KCl, KClO3, K2CO3 and KClO4) to produce an intense plasma at the target surface. Several distinct infrared (IR) atomic emission signatures were observed from all sodium and potassium containing compounds. The atomic emission lines observed from the investigated samples matched assigned transitions of neutral sodium and potassium atoms published in the National Institute of Standards and Technology (NIST) atomic database. In addition to the intense atomic lines, the rst evidence of molecular LIBS emission structures were observed at ˜10.0 m in KClO3 and NaClO3 for the chlorate anion (ClO3 --1), at ˜6.7 to 8.0 mum in KNO3 and NaNO 3 for the nitrate anion (NO3--1 ), ˜8.0 to 10.0 mum in KClO4 and NaClO4 for perchlorate anion (ClO4--1 ), and ˜6.88 mum and 11.53 mum in Na2CO3 for the carbonate anion (CO3--1 ). The observed molecular emission showed strong correlation with the conventional Fourier Transform Infrared Spectrometry (FTIR) absorption spectra of the investigated samples. IR LIBS was also applied to determine the limit of detection (LOD) for the perchlorate anion in KClO4 using the 8.0 -11.0 mum IR-LIBS emission band. The calibration curve of ClO4 in KClO4 was constructed using peak and integrated emission intensities for known concentrations of mixed KClO4/NH4NO3 samples. The

  8. Application of preparation process of high pure chlorine dioxide by electrolysis method in water treatment%电解法制高纯二氧化氯工艺在水处理中的应用

    Institute of Scientific and Technical Information of China (English)

    刘艳霞; 韩瑞雄; 赵红; 周俊波

    2011-01-01

    为了开发经济实用的二氧化氯消毒工艺,对电解法制备高纯二氧化氯工艺在水处理中的运用进行了研究.在最佳条件下,电解氯酸盐自动催化循环制备的二氧化氯纯度可达98%左右.通过二氧化氯杀菌除藻试验,讨论了二氧化氯用量以及原水pH对细菌、叶绿素a、藻类的去除率的影响.结果表明,二氧化氯用量在2 mg/L以上时,3者的去除率均达到90%以上.当二氧化氯用量为2 mg/L、原水pH为6~9时,3者的去除率不发生显著变化,并且二氧化氯的剩余质量浓度均控制在0.5 mg/L以下.消毒成本:生产1 kg二氧化氯成本可以控制在6元以内,当二氧化氯用量在0.5 ~2 mg/L时,1 t水的消毒成本为0.003~ 0.012元.%To develop an economical and practical disinfection technology of chlorine dioxide, the application of preparation process of high pure chlorine dioxide by electrolysis method in water treatment was studied. Under the best conditions, the purity of chlorine dioxide, which was prepared by electrolysis of chlorate solution with auto-catalytic cycling,can reach about 98% . Through the experiments of algae removal and sterilization,the influences of concentration of chlorine dioxide and pH of raw water on the removal rate of bacteria,chlorophyll A ,and algal were discussed. Results showed that when the mass concentration of chlorine dioxide was above 2 mg/L, the removal rates of bacteria, chlorophyll A, and algal could all reached above 90% . When the mass concentration of chlorine dioxide was 2 mg/L and pH of raw water was at 6 ~9,the removal rates of them could not occur significant change, and the mass concentration of residual chlorine dioxide was all under 0. 5 mg/L. Though accounting for the cost of water disinfection, the cost of per kilogram chlorine dioxide in the process can be controlled less than RMB 6 Yuan. When the invested amount of chlorine dioxide was at 0.5 ~2 mg/L,and the cost of per ton water disinfection

  9. Diversity and Biomineralization of Microaerophilic Iron-oxidizing Bacteria in Paddy Soil%水稻土嗜中性微好氧亚铁氧化菌多样性及微生物成矿研究

    Institute of Scientific and Technical Information of China (English)

    陈娅婷; 李芳柏; 李晓敏

    2016-01-01

    FeOB in paddy soil. In this study, gradient tubes with opposing gradient Fe(Ⅱ) and O2 were used to enrich and isolate microaerophilic FeOB from paddy soil, where 16S rRNA gene sequencing methods were used to profile the microbial diversity and distribution of FeOB in continuous cultivation and then the ability of Fe(Ⅱ) oxidation by the isolated FeOB and the Fe(Ⅲ) products were tested as well. The results showed thatAzospira,Magnetospirillum,ClostridiumandRhodoplaneswere abundant in the cultured communities. A mixture of several species remained together till the last stage of isolation, which might due to the syntrophic associations among the FeOBs. Among them, Azospira was the dominant FeOB with a relative abundance of 63.9%. Azospira is a well-known nitrate-reducing FeOB, which is capable of utilizing nitrate, chlorate or perchlorate as alternative electron acceptors. The isolated FeOB mixture actively oxidized Fe(Ⅱ), the concentration of HCl-Fe was 6.9 mmol·L-1on day 15.XRD results revealed that amorphous iron oxides were formed as the products of microbial iron oxidation. TEM results showed that cells of microaerophilic FeOB were rod-shaped with globular shaped particles sparsely deposited on the surface or around the cell, which might consist of amorphous Fe(Ⅲ) oxides. Overall, our results revealed that denitrifying bacteria might be capable of microaerophilic Fe(Ⅱ) oxidation which could be stimulated in the oxic-anoxic interface in paddy soil, and amorphous iron oxides were formed as microbial Fe(Ⅱ) oxidation by such bacteria.

  10. Search for nitrates on Mars by the Sample Analysis at Mars (SAM) Instrument

    Science.gov (United States)

    Navarro-Gonzalez, Rafael; Stern, Jennifer; Freissinet, Caroline; Franz, Heather; McKay, Christopher; Coll, Patrice; Sutter, Brad; Archer, Doug; McAdam, Amy; Cabane, Michel; Ming, Douglas; Glavin, Daniel; Eigenbrode, Jennifer; Leshin, Laurie; Wong, Michael; Atreya, Sushil; Wray, James; Steele, Andrew; Buch, Arnaud; Prats, Benito

    2014-05-01

    compared with analog studies of mixtures of nitrates and perchlorates [10]. [1] Luhmann, J.G., Johnson E. And Zhang, M.H.G.: 1992, Evolutionary impact of sputtering of the Martian atmosphere by O+ pickup ions. Geophys. Res. Lett. 19, 2151-2154. [2] Jakosky, B.M. Pepin, R.O., Johnsom, R.E. and Fox, J.L: 1994, Mars atmospheric loss and isotopic fractionation by solar-wind-induced sputtering and photochemical escape. Icarus, 111, 271-288. [3] Melosh, H.J. and Vickery, A.M.: 1989, Impact erosion of the primordial atmosphere of Mars. Nature 338, 487-489. [4] Mancinelli, R.L. and McKay, C.P. :1988, The evolution of nitrogen cycling. Origins Life 18, 311-325. [5] Manning, C.V., McKay, C.P., and Zahnle, K.J.: 2008, The nitrogen cycle on Mars: Impact decomposition of near-surface nitrates as a source for a nitrogen steady state. Icarus, 197, 60-64. [6] Smith, M.L., Claire, M.W., Catling, D.C., and Zahnle, K.J.: 2014, The formation of sulfate, nitrate and perchlorate salts in the martian atmosphere. Icarus 231, 51-64. [7] Hecht, M. H., Kounaves, S.P., Quinn, R.C., West, S.J., Young, S.M.M., Ming, D.W.,Catling, D.C., Clark, B.C., Boynton, W.V.,Hoffman, J., DeFlores, L.P., Gospodinova, K., Kapit, J., and Smith,P.H.: 2009, Detection of Perchlorate and the Soluble Chemistry of Martian Soil at the Phoenix Lander Site. Science, 32, 64-67. [8] Grady, M.M., Wright, I. P., and Pillinger C. T.: 1995, Search for nitrates in Martian meteorite. J. Geophys. Res. 100, 5449. [9] Kounaves, S.P., Carrier, B.L., O'Neil, G.D., Stroble, S.T., Claire, M.W.: 2013, Evidence of martian perchlorate, chlorate, and nitrate in Mars meteorite EETA79001: implications for oxidants and organics, Icarus, doi: http://dx.doi.org/10.1016/j.icarus.2013.11.012. [10] Support from the following grants is acknowledged: IN106013 and CONACYT 98466.

  11. Nickel Titanium Instrument with TF and Protaper for the Efficacy of Root Canal Therapy%机用镍钛器械TF和Protaper用于根管治疗的疗效观察

    Institute of Scientific and Technical Information of China (English)

    黄自理; 黄永坚

    2014-01-01

    Objective To machine nickel titanium mechanical TF and Protaper for the clinical curative ef ects of root canal therapy. Methods The hospital in 2013 May-12 months of Oral Department of internal medicine, 120 patients as the research object, the need for root canal treatment af ected teeth was 142, were randomly divided into observation group and control group each 71, observation group with dental nickel titanium files instruments in root canal preparation using TF machine, the control group teeth with nickel titanium files instruments in root canal preparation by Protaper. Two groups of patients after root canal preparation with sodium chlorate cleaning teeth, root canal is completely dry after use Calcium Hydroxide Paste, confirm the root canal does not affect the daily life of the patients with and 7 days is up, use warm gut a percha and AHplus root canal paste on root canal fil ing with vertical hot pressing method. Results In the observation group, 5 cases of overfil ing root exists, the control group had 10 cases of root tip there is a smal amount of overfil ing, no gut a percha beyond the apical foramen teeth, no charge less teeth occurred. The X light display, control group patients after root canal preparation, the root canal fluency is good, root canal morphology did not change, root canal preparation standard. Root canal preparation time of observation group was significantly shorter compared with the control group, and the P<0.05 has statistical significance. Conclusion TF machine used nickel titanium files instruments in root canal preparation time is shorter than Protaper, nickel titanium files instruments in root canal preparation is better than the Protaper TF machine.%目的:探讨机用镍钛机械TF和Protaper用于根管治疗的临床疗效。方法本次研究选取本院口腔内科2013年5月~12月的患者120例作为研究对象,其中需要进行根管治疗的患牙为142颗,随机分成观察组与对照组各71颗,观察组患牙

  12. On line pre-concentration for simultaneous determination of low molecular weight organic acids and inorganic anions in Amazonian river water samples employing ion chromatography with conductivity detection Pré-concentração em linha para a determinação simultânea de ácidos carboxílicos de baixo peso molecular e ânions inorgânicos em amostras de rios da Amazônia empregando cromatografia de íons com detecção por condutividade elétrica

    Directory of Open Access Journals (Sweden)

    Cristiane Azevedo Tumang

    2009-01-01

    Full Text Available An ion chromatography procedure, employing an IonPac AC15 concentrator column was used to investigate on line preconcentration for the simultaneous determination of inorganic anions and organic acids in river water. Twelve organic acids and nine inorganic anions were separated without any interference from other compounds and carry-over problems between samples. The injection loop was replaced by a Dionex AC15 concentrator column. The proposed procedure employed an auto-sampler that injected 1.5 ml of sample into a KOH mobile phase, generated by an Eluent Generator, at 1.5 mL min-1, which carried the sample to the chromatographic columns (one guard column, model AG-15, and one analytical column, model AS15, with 250 x 4mm i.d.. The gradient elution concentrations consisted of a 10.0 mmol l-1 KOH solution from 0 to 6.5 min, gradually increased to 45.0 mmol l-1 KOH at 21 min., and immediatelly returned and maintained at the initial concentrations until 24 min. of total run. The compounds were eluted and transported to an electro-conductivity detection cell that was attached to an electrochemical detector. The advantage of using concentrator column was the capability of performing routine simultaneous determinations for ions from 0.01 to 1.0 mg l-1 organic acids (acetate, propionic acid, formic acid, butyric acid, glycolic acid, pyruvate, tartaric acid, phthalic acid, methanesulfonic acid, valeric acid, maleic acid, oxalic acid, chlorate and citric acid and 0.01 to 5.0 mg l-1 inorganic anions (fluoride, chloride, nitrite, nitrate, bromide, sulfate and phosphate, without extensive sample pretreatment and with an analysis time of only 24 minutes.A metodologia analítica foi desenvolvida empregando coluna pré-concentradora AC15 em linha na cromatografia iônica na determinação simultânea de ânions orgânicos e inorgânicos, com uso de coluna de guarda AG15 e analítica AS15, 250 x 4 mm i.d. (Dionex Corp.. O gradiente de concentração do eluente

  13. Preparation of disinfectant containing both chlorine dioxide and chlorine for safe urban reuse%复合二氧化氯的制备及其用于城市污水回用消毒

    Institute of Scientific and Technical Information of China (English)

    樊金红; 王红武; 马鲁铭

    2012-01-01

    在酸性环境中通过NaCl电解协同NaClO2化学氧化方法制备的复合二氧化氯溶液中ClO2和自由氯浓度分别达到70%和20%左右,系统地研究了电流密度(A)、NaClO2与NaCl质量比(B)、电解时间(C)对复合溶液中组分浓度和质量百分数的影响,并将复合溶液用于城市污水二级处理出水的消毒.结果表明,复合溶液中自由氯的浓度主要受因素C和A的影响,ClO2的浓度主要受因素C和B的影响,而A对副产物ClO-2和ClO-3的影响最大.总大肠菌群数在105~108个?L-1的城市污水二级处理出水采用复合溶液消毒时,当其中ClO2投加量为4mg? L-1,自由氯含量不低于1.20 mg?L-1,经30 min接触后出水生物学指标满足GB/T 18920-2002的要求.既降低了消毒剂的使用量,又减少了消毒副产物ClO-2的生成.%To achieve simultaneously maximum disinfection and minimum toxicity a mix disinfectant of chlorine dioxide and chlorine are found to be efficient for disinfection of drinking water and urban reused waste-water. However, transportation and reservation of the mixture may threat to environmental safety. Therefore, on-site preparation is necessary for field use. At present, preparation methods of the mix disinfectant have chemical reduction of sodium chlorate and electrolysis of sodium chloride, and the content of chlorine dioxide in mixture obtained is usually below 30%. To get high chlorine dioxide content, a method for the preparation of the mix disinfectant was proposed : electrolyzing sodium chloride (NaCl) was followed by a chemical oxidation of sodium chlorite (NaClC2) in an undivided electrolysis reactor, in which the content of C1O2 in the mix disinfectant can be controlled. The effect of current density (A), mass ratio of NaCIO2: NaCl (B), electrolysis time (C) on the concentration and mass percentage of CIO2, free chlorine, ClO-2 and C1O-3 was investigated systematically. Under the electrolysis conditions: current density 41. 67-83. 33 A