WorldWideScience

Sample records for bromates

  1. Modeling bromate formation during ozonation

    OpenAIRE

    JARVIS, Peter; Parsons, Simon A.; Smith, Rosie

    2007-01-01

    Bromate formation has been identified as a significant barrier in the application of ozone during water treatment for water sources that contain high levels of bromide. Bromate has been identified as a possible human carcinogen and bromate levels in drinking water are strictly controlled at 10 mu g/L in most developed countries. Various models have been proposed to model bromate formation during ozonation based on raw water quality, ozone dose and contact time. Two main appr...

  2. Bromate Reduction by Denitrifying Bacteria

    OpenAIRE

    Hijnen, W.; Voogt, R.; Veenendaal, H. R.; Jagt, H.; van der Kooij, D

    1995-01-01

    In the presence of bromide, ozonation as applied in water treatment results in the formation of bromate, an ion with carcinogenic properties. The reduction of bromate by mixed bacterial populations as well as pure cultures was studied under laboratory conditions. Bromate was reduced to bromide by a mixed bacterial population with and without a preceding nitrate reduction step in an anaerobically incubated medium with ethanol as the energy and carbon source at 20 and 25 deg C. The predominatin...

  3. 21 CFR 172.730 - Potassium bromate.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Potassium bromate. 172.730 Section 172.730 Food and... Specific Usage Additives § 172.730 Potassium bromate. The food additive potassium bromate may be safely... malt from the treatment does not exceed 75 parts per million of bromate (calculated as Br), and the...

  4. 186 183 Potassium Bromate Content of Bread

    African Journals Online (AJOL)

    2008-12-02

    Dec 2, 2008 ... This study has shown that in spite of National Agency for Food and Drug Administration and Control. (NAFDAC) campaign for bromate-free ... agents' flavourings, yeasts, and bread improver. Yeast feed on sugar to produce .... mutagenic studies show that potassium bromate is a potential cancer initiator.

  5. Bromate removal by anaerobic bacterial community: mechanism and phylogenetic characterization.

    Science.gov (United States)

    Assunção, Ana; Martins, Mónica; Silva, Gonçalo; Lucas, Helena; Coelho, Maria Rosário; Costa, Maria Clara

    2011-12-15

    A highly bromate resistant bacterial community and with ability for bromate removal was obtained from a sulphate-reducing bacteria enrichment consortium. This community was able to remove 96% of bromate and 99% of sulphate from an aqueous solution containing 40 μM bromate and 10 mM sulphate. Moreover, 93% of bromate was removed in the absence of sulphate. Under this condition bromate was reduced stoichiometrically to bromide. However, in the presence of sulphate only 88% of bromate was reduced to bromide. Although, bromate removal was not affected by the absence of sulphate, this anion promoted a modification on the structure of the bacterial community. Phylogenetic analysis of 16S rRNA gene showed that the community grown in the presence of bromate and sulphate was mainly composed by bacteria closely to Clostridium and Citrobacter genera, while the community grown in the absence of sulphate was predominantly composed by Clostridium genus. It is the first time that Clostridium and Citrobacter genera are reported as having bromate removal ability. Furthermore, bromate removal by the consortium predominantly composed by Clostridium and Citrobacter genera occurred by enzymatic reduction and by extracellular metabolic products, while the enzymatic process was the only mechanism involved in bromate removal by the consortium mainly composed by Clostridium genus. Copyright © 2011 Elsevier B.V. All rights reserved.

  6. Drinking water toxicity study of the environmental contaminant--Bromate.

    Science.gov (United States)

    Dongmei, Liu; Zhiwei, Wang; Qi, Zhu; Fuyi, Cui; Yujuan, Shan; Xiaodong, Liu

    2015-12-01

    Bromate is a byproduct of water disinfection that is produced when waters contain bromide treated with ozone. To investigate the level of the toxicity of bromate and find the most sensitive indicators in a short time, a series of toxicological assessments were conducted including the acute toxicity, cumulative toxicity, genetic toxicity and subacute toxicity of bromate (using Potassium Bromate to represent bromate). The LD50 of orally administered Potassium Bromate was 215 mg/kg in Wistar rats and 464 mg/kg in ICR mice. The cumulative toxicity of Potassium Bromate was not obvious. The Ames test, mouse bone marrow cell micronucleus test and mouse sperm abnormality test did not indicate mutagenicity. The results of the subacute study did not exhibit significant differences in most of the parameters, except the white blood cell count, which was significantly decreased in male rats. In addition, Potassium Bromate influenced the albumin, creatinine, total cholesterol, triglycerides and glucose levels in male rats to various extents. A thorough analysis of the above tests clearly demonstrates that bromate has toxicity, not obvious cumulative toxicity and the white blood cell count can be used as an indicator to reflect the toxicity of bromate and investigate bromate's toxic mechanism. Copyright © 2015 Elsevier Inc. All rights reserved.

  7. 186 183 Potassium Bromate Content of Bread

    African Journals Online (AJOL)

    2008-12-02

    Dec 2, 2008 ... that potassium bromate affects the nutritional quality of bread as the main vitamins available in bread are ... inhalation, abdominal pain, diarrhoea, nausea, vomiting, kidney failure, hearing loss as well as ... because a cancer warning is required on the label (Starr, 2002). The World Health. Organisation in ...

  8. Acute Renal Failure following Accidental Potassium Bromate ...

    African Journals Online (AJOL)

    Accidental poisoning is common in children. Potassium bromate is a commonly used additive and raising agent in many edibles particularly bread, a staple food worldwide, yet its accidental poisoning has hitherto, not been documented in Nigeria. We report an unusual case of acute renal failure following accidental ...

  9. BROMATE: A CONCERN FOR DEVELOPMENTAL NEUROTOXICITY?

    Science.gov (United States)

    In February of 2005 a workshop was held to evaluate the state-of-the-science of bromate toxicity. The workshop was sponsored by the American Water Works Association - Research Foundation, the Southern Nevada Water Authority, Fairfax Water Authority, and Miami University. This m...

  10. Evidence of specialized bromate-reducing bacteria in a hollow fiber membrane biofilm reactor.

    Science.gov (United States)

    Martin, K J; Downing, L S; Nerenberg, R

    2009-01-01

    Bromate is a carcinogenic disinfection by-product formed from bromide during ozonation or advanced oxidation. We previously observed bromate reduction in a hydrogen-based, denitrifying hollow fiber membrane biofilm reactor (MBfR). In this research, we investigated the potential existence of specialized bromate-reducing bacteria. Using denaturing gradient gel electrophoresis (DGGE), we compared the microbial ecology of two denitrifying MBfRs, one amended with nitrate as the electron acceptor and the other with nitrate plus bromate. The DGGE results showed that bromate exerted a selective pressure for a putative, specialized bromate-reducing bacterium, which developed a strong presence only in the reactor with bromate. To gain further insight into the capabilities of specialized, bromate-reducing bacteria, we explored bromate reduction in a control MBfR without any primary electron acceptors. A grown biofilm in the control MBfR reduced bromate without previous exposure, but the rate of reduction decreased over time, especially after perturbations resulting in biomass loss. The decrease in bromate reduction may have been the result of the toxic effects of bromate. We also used batch tests of the perchlorate-reducing pure culture, Dechloromonas sp. PC1 to test bromate reduction and growth. Bromate was reduced without measurable growth. Based on these results, we speculate bromate's selective pressure for the putative, specialized BRB observed in the DGGE was not growth related, but possibly based on resistance to bromate toxicity.

  11. Reduction of Bromate Formation During Ozonation of Drinking Water

    DEFF Research Database (Denmark)

    Antoniou, Maria; Sichel, C.; Andre, K.

    This study focused on the prevention of carcinogenic bromate formation during ozonation of tap water from the DTU university campus. To achieve this, different pre-treatments including pH-adjustment, ammonia addition and chlorine-ammonia addition, were tested. Formation of bromated was drastically...

  12. Potassium bromate content of some baked breads sold in Kano ...

    African Journals Online (AJOL)

    Background: Potassium bromate is an additive used by some bakers to make the bread rise rapidly, create a good texture in the finished product and to give bulkiness to the dough. Objective: The main objective of this work was to assess the potassium bromate residues of some baked breads sold in some selected local ...

  13. Potassium Bromate Content of Bread Produced in Sokoto Metropolis ...

    African Journals Online (AJOL)

    Fifteen different bread samples were randomly collected from various local bakeries located in Sokoto metropolis. The samples were analysed for presence and quantity of potassium bromate. All the samples were analysed using the redox titrimetric method for the detection of potassium bromate. All the samples contained ...

  14. Accidental Potassium Bromate Poisoning Causing Acute Renal Failure

    OpenAIRE

    Adeleke SI; Asani MO

    2009-01-01

    Accidental poisoning is common in children. Potassium bromate is commonly used additive and raising agent in many edibles especially bread which is a staple food in Nigeria. This communication is that of an unusual case of acute renal failure following accidental ingestion of potassium bromate tablets.

  15. Accidental Potassium Bromate Poisoning Causing Acute Renal Failure

    Directory of Open Access Journals (Sweden)

    Adeleke SI

    2009-05-01

    Full Text Available Accidental poisoning is common in children. Potassium bromate is commonly used additive and raising agent in many edibles especially bread which is a staple food in Nigeria. This communication is that of an unusual case of acute renal failure following accidental ingestion of potassium bromate tablets

  16. The Effect Of Potassium Bromate On Some Haematological ...

    African Journals Online (AJOL)

    Summary: Potassium bromate used widely in foods has been associated with various complications in humans. However there is paucity of literature on adverse effects on haematological parameters. Thus we decided to carry out an experimental study to determine the effects of potassium bromate on some blood indices ...

  17. A Case of Cochlear Implantation in Bromate-Induced Bilateral Sudden Deafness

    OpenAIRE

    Eom, Tae-Ho; Lee, Sungsu; Cho, Hyong-Ho; Cho, Yong-Beom

    2015-01-01

    Despite the well-established nature of bromate-induced ototoxicity, cochlear implantation after bromate intoxication has been rarely documented. We hereby present a case of a 51-year-old female deafened completely after bromate ingestion. Her hearing was not restored by systemic steroid treatment and hearing aids were of no use. A cochlear implantation was performed on her right ear 3 months after the bromate ingestion. In bromate intoxication cases, early monitoring of hearing level is neces...

  18. Bromate removal from aqueous solutions by ordered mesoporous carbon.

    Science.gov (United States)

    Xu, Chunhua; Wang, Xiaohong; Shi, Xiaolei; Lin, Sheng; Zhu, Liujia; Che, Yaming

    2014-01-01

    We investigated the feasibility of using ordered mesoporous carbon (OMC) for bromate removal from water. Batch experiments were performed to study the influence of various experimental parameters such as the effect of contact time, adsorbent dosage, initial bromate concentration, temperature, pH and effect of competing anions on bromate removal by OMC. The adsorption kinetics indicates that the uptake rate ofbromate was rapid at the beginning: 85% adsorption was completed in 1 h and equilibrium was achieved within 3 h. The sorption process was well described with pseudo-second-order kinetics. The maximum adsorption capacity of OMC for bromate removal was 17.6 mg g(-1) at 298 K. The adsorption data fit the Freundlich model well. The amount of bromate removed was found to be proportional to the influent bromate concentration. The effects of competing anions and solution pH (3-11) were negligible. These limited data suggest that OMC can be effectively utilized for bromate removal from drinking water.

  19. Bromate removal from water by granular ferric hydroxide (GFH).

    Science.gov (United States)

    Bhatnagar, Amit; Choi, Yanghun; Yoon, Yeojoon; Shin, Yongsoon; Jeon, Byong-Hun; Kang, Joon-Wun

    2009-10-15

    The feasibility of granular ferric hydroxide (GFH) for bromate removal from water has been studied. Batch experiments were performed to study the influence of various experimental parameters such as effect of contact time, initial bromate concentration, temperature, pH and effect of competing anions on bromate removal by GFH. The adsorption kinetics indicates that uptake rate of bromate was rapid at the beginning and 75% adsorption was completed in 5 min and equilibrium was achieved within 20 min. The sorption process was well described by pseudo-second-order kinetics. The maximum adsorption potential of GFH for bromate removal was 16.5 mg g(-1) at 25 degrees C. The adsorption data fitted well to the Langmuir model. The increase in OH peak and absence of Br-O bonding in FTIR spectra indicate that ion-exchange was the main mechanism during bromate sorption on GFH. The effects of competing anions and solution pHs (3-9) were negligible. Results of the present study suggest that GFH can be effectively utilized for bromate removal from drinking water.

  20. Potassium Bromate Assay by Redox Titrimetry Using Arsenic Trioxide

    OpenAIRE

    Smeller, Johanna M.; Leigh, Stefan D.

    2003-01-01

    Bromate, a disinfectant, is one of the analytes of interest in wastewater analysis. Environmental laboratories have a regulatory need for their measurements to be traceable to NIST standards. Bromate is not currently certified as a NIST Standard Reference Material (SRM). Therefore, a traceable assay of potassium bromate (KBrO3) is needed. KBrO3 was dissolved in water and assayed by redox titrimetry using arsenic trioxide (As2O3). A nominal (0.1 g) sample of As2O3 was dissolved in 10 mL of 5 m...

  1. Characterization of bromate-reducing bacterial isolates and their potential for drinking water treatment.

    Science.gov (United States)

    Davidson, Andrew N; Chee-Sanford, Joanne; Lai, Hoi Yi Mandy; Ho, Chi-hua; Klenzendorf, J Brandon; Kirisits, Mary Jo

    2011-11-15

    The objective of the current study was to isolate and characterize several bromate-reducing bacteria and to examine their potential for bioaugmentation to a drinking water treatment process. Fifteen bromate-reducing bacteria were isolated from three sources. According to 16S rRNA gene sequencing, the bromate-reducing bacteria are phylogenetically diverse, representing the Actinobacteria, Bacteroidetes, Firmicutes, and α-, β-, and γ-Proteobacteria. The broad diversity of bromate-reducing bacteria suggests the widespread capability for microbial bromate reduction. While the cometabolism of bromate via nitrate reductase and (per)chlorate reductase has been postulated, five of our bromate-reducing isolates were unable to reduce nitrate or perchlorate. This suggests that a bromate-specific reduction pathway might exist in some microorganisms. Bioaugmentation of activated carbon filters with eight of the bromate-reducing isolates did not significantly decrease start-up time or increase bromate removal as compared to control filters. To optimize bromate reduction in a biological drinking water treatment process, the predominant mechanism of bromate reduction (i.e., cometabolic or respiratory) needs to be assessed so that appropriate measures can be taken to improve bromate removal. Copyright © 2011 Elsevier Ltd. All rights reserved.

  2. [Acute Toxic Effects of Bromate on Aquatic Organisms].

    Science.gov (United States)

    Wang, Zhi-wei; Liu, Dong-mei; Zhang, Wen-juan; Cui, Fu-yi

    2016-02-15

    Acute toxic effects of potassium bromate, sodium bromate and potassium bromide on luminescent bacteria, water flea, green alga and zebrafish were studied using standard toxic testing methods. The results showed that the pollutants had no effect on the luminous intensity of luminescent bacteria. The 96 h EC5. of potassium bromate on Scenedesmus obliquus was 738.18 mg x L(-1), 48 h EC50 on Daphnia magna and Moina was 154.01 mg x L(-1) was 161.80 mg x L(-1), while 48 h LC50 was 198 52 mg x L(-1), 175.68 mg x L(-1), and 96 h LC50 on zebrafish was 931.4 mg x L(-1). The 96 h EC50 of sodium bromate on Scenedesmus obliquus was 540.26 mg x L(-1), 48 h EC50 Daphnia magna and Moina was 127.90 mg x L(-1), 111.07 mg x L(-1), while 48 h LC50 was 161.80 mg x L(-1), 123.47 mg x L(-1), and 96 h LC50 on zebrafish was 1065.6 mg x L(-1). But the effects of potassium bromide on the above several kinds of aquatic organisms were far smaller than those of potassium bromate and sodium bromate. The toxic effects on test organisms were due to the impacts of bromate after the comparison of different pollutants, and the effects were more obvious with the increase of exposure time. The order of sensitivity to the toxic effects of bromate was Daphnia magna, Moina > Scenedesmus obliquus > zebrafish > Chlorella vulgaris, luminescent bacteria.

  3. Kinetics and Mechanism of the Oxidation of Menthol by Potassium Bromate in Acidic Solution

    OpenAIRE

    Ravikant na; Ms. Meena; Shrikant Sharma

    2014-01-01

    No suitable method is available for the estimation of menthol, hence in all kinetic results reported in this chapter, menthol was in excess over potassium bromate and the stoichiometry was also determined under the experimental conditions where menthol (substrate) was in excess over potassium bromate (oxidant). Present study was focused on the analysis of kinetics and mechanism of oxidation of neomenthol by potassium bromate in acidic medium. For oxidizing neomenthol, potassium bromate stock ...

  4. Kinetics and Mechanism of the Oxidation of Neomenthol by Potassium Bromate in Acidic Solution

    OpenAIRE

    Ravikant na

    2014-01-01

    Present study was focused on the analysis of kinetics and mechanism of oxidation of neomenthol by potassium bromate in acidic medium. For oxidizing neomenthol, potassium bromate stock solution (5.0×10─2 mol. dm─3) was prepared by dissolving exactly weighed quantity of potassium bromate in doubly distilled water. The suitable reaction mixtures were prepared and left at 313 K for over 24 hours to ensure complete oxidation of neomenthol15. The unreacted potassium bromate was determined iodometri...

  5. BROMATE-INDUCED TRANSCRIPTIONAL CHANGES IN LONG-EVANS RAT KIDNEYS

    Science.gov (United States)

    Bromate-Induced Transcriptional Changes in Long-Evans Rat Kidneys.Ozone disinfection of surface waters containing bromide ion (Br-) results in the oxidation of bromide to bromate, which can be found in finished drinking water as a by-product. Potassium bromate (KBrO3)...

  6. Options and limitations for bromate control during ozonation of wastewater.

    Science.gov (United States)

    Soltermann, Fabian; Abegglen, Christian; Tschui, Manfred; Stahel, Sandro; von Gunten, Urs

    2017-06-01

    Wastewater treatment plants (WWTPs) are important point sources for micropollutants, which are harmful to freshwater organisms. Ozonation of wastewater is a powerful option to abate micropollutants, but may result in the formation of the potentially toxic oxidation by-product bromate in bromide-containing wastewaters. This study investigates options to reduce bromate formation during wastewater ozonation by (i) reducing the bromide concentration of the wastewater, (ii) lowering the ozone dose during wastewater treatment and (iii) adding hydrogen peroxide to limit the lifetime of ozone and quench the intermediates of the bromate formation pathway. Two examples demonstrate that a high share of bromide in wastewater can originate from single point sources (e.g., municipal waste incinerators or landfills). The identification of major point sources requires laborious sampling campaigns, but may facilitate the reduction of the bromide load significantly. To reduce the bromate formation by lowering the ozone dose interferes with the aim to abate micropollutants. Therefore, an additional treatment is necessary to ensure the elimination of micropollutants. Experiments at a pilot-plant illustrate that a combined treatment (ozone/powdered activated carbon) allows to eliminate micropollutants with low bromate yields. Furthermore, the addition of hydrogen peroxide was investigated at bench-scale. The bromate yields could be reduced by ∼50% and 65% for a hydrogen peroxide dose of 5 and 10 mg L(-1), respectively. In conclusion, there are options to reduce the bromate formation during wastewater ozonation, however, they are not simple with sometimes limited efficiency. Copyright © 2017 Elsevier Ltd. All rights reserved.

  7. Kinetics and Mechanism of the Oxidation of Neomenthol by Potassium Bromate in Acidic Solution

    Directory of Open Access Journals (Sweden)

    Ravikant na

    2014-03-01

    Full Text Available Present study was focused on the analysis of kinetics and mechanism of oxidation of neomenthol by potassium bromate in acidic medium. For oxidizing neomenthol, potassium bromate stock solution (5.0×10─2 mol. dm─3 was prepared by dissolving exactly weighed quantity of potassium bromate in doubly distilled water. The suitable reaction mixtures were prepared and left at 313 K for over 24 hours to ensure complete oxidation of neomenthol15. The unreacted potassium bromate was determined iodometrically and the results indicate that one mole of potassium bromate is consumed for every three moles of neomenthol which leads to the formation of menthone (ketone.

  8. Reduction of bromate by biogenic sulfide produced during microbial sulfur disproportionation.

    Science.gov (United States)

    Chairez, Monserrat; Luna-Velasco, Antonia; Field, Jim A; Ju, Xiumin; Sierra-Alvarez, Reyes

    2010-04-01

    Bromate (BrO(3) (-)) is a carcinogenic contaminant formed during ozonation of waters that contain trace amounts of bromide. Previous research shows that bromate can be microbially reduced to bromide using organic (i.e. acetate, glucose, ethanol) and inorganic (H(2)) electron-donating substrates. In this study, the reduction of bromate by a mixed microbial culture was investigated using elemental sulfur (S(0)) as an electron donor. In batch bioassays performed at 30 degrees C, bromate (0.30 mM) was completely converted to bromide after 10 days and no accumulation of intermediates occurred. Bromate was also reduced in cultures supplemented with thiosulfate and hydrogen sulfide as electron donor. Our results demonstrated that S(0)-disproportionating microorganisms were responsible for the reduction of bromate in cultures spiked with S(0) through an indirect mechanism involving microbial formation of sulfide and subsequent abiotic reduction of bromate by the biogenic sulfide. Confirmation of this mechanism is the fact that bromate was shown to undergo rapid chemical reduction by sulfide (but not S(0) or thiosulfate) in abiotic experiments. Bromate concentrations above 0.30 mM inhibited sulfide formation by S(0)-disproportionating bacteria, leading to a decrease in the rate of bromate reduction. The results suggest that biological formation of sulfide from by S(0) disproportionation could support the chemical removal of bromate without having to directly use sulfide as a reagent.

  9. Kinetics and Mechanism of the Oxidation of Menthol by Potassium Bromate in Acidic Solution

    Directory of Open Access Journals (Sweden)

    Ravikant na

    2014-06-01

    Full Text Available No suitable method is available for the estimation of menthol, hence in all kinetic results reported in this chapter, menthol was in excess over potassium bromate and the stoichiometry was also determined under the experimental conditions where menthol (substrate was in excess over potassium bromate (oxidant. Present study was focused on the analysis of kinetics and mechanism of oxidation of neomenthol by potassium bromate in acidic medium. For oxidizing neomenthol, potassium bromate stock solution (5.0×10─2 mol. dm─3 was prepared by dissolving exactly weighed quantity of potassium bromate in doubly distilled water. The suitable reaction mixtures were prepared and left at 313 K for over 24 hours to ensure complete oxidation of neomenthol. The unreacted potassium bromate was determined iodometrically and the results indicate that one mole of potassium bromate is consumed for every three moles of neomenthol and leads to the formation of menthone (ketone.

  10. Spectrophotometeric Determination of Bromate in Bread by the ...

    African Journals Online (AJOL)

    DR. MIKE HORSFALL

    Hazard Analysis Critical Control Points (HACCP) guidelines acceptable world wide. In addition, they should explore such other natural bread improvers like AMIPAN and unbrominated bread improver, SS103U made in. Malaysia. REFERENCES. Akunyili, D N (2004). Medical Nigeria: Potassium bromate in bread… what ...

  11. Histopathologic effect of potassium bromate on the kidney of adult ...

    African Journals Online (AJOL)

    Objective: We aimed to demonstrate the histopathologic effects of potassium bromate (KBrO ) on the kidney tissues of rats following 3 short-term and long-term exposures. Method: Twenty young wistar rats of weights 180-250g were divided into three groups. The control group A was sub-divided into two groups of three rats ...

  12. Adsorption / reduction of bromate from drinking water using GAC ...

    African Journals Online (AJOL)

    This study investigated the feasibility of using granular activated carbon (GAC) to remove bromate (BrO3-) from drinking water through batch experiments, rapid small-scale column tests (RSSCT) and a pilot-scale study. The results indicated that the GAC capacity for BrO3- removal was dependent on the GAC surface ...

  13. catalyzed oxidation of some amino acids by acid bromate

    African Journals Online (AJOL)

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    Srivastava, S., Tripathi, H. and Singh, K. (2001). Ruthenium(III) Catalysed oxidation of glycerol by acidified KBrO3.Transition Metal. Chemistry 26:727–729. 19. Subramanian, N. Venkata and Thiagarajan, V. (1969). Kinetics and mechanism of ruthenium tetroxide catalysed oxidation of cyclic alcohols by bromate in a base.

  14. The mutagenic potentials of potassium bromate and some ...

    African Journals Online (AJOL)

    GREGO

    2007-04-16

    Apr 16, 2007 ... This revealed that potassium bromate is mutagenic in bacteria and could be said to possess carcinogenic potentials. Key words: Food additives, E.coli, Ames spot assay, Mutant strains. INTRODUCTION. Food additives are substances added to preserve flavour or improve the taste and appearance of food.

  15. the effect of potassium bromate on some haematological parameters ...

    African Journals Online (AJOL)

    Daniel Owu

    wave hair solution (Ueno 2000). Potassium bromate is a substance that has a vapour density of 5.8 (air=1) and density of 3.27. (gcm3) and when in contact with combustible material may cause fire. It is incompatible with organics, reducing agents, aluminum, and finely powdered metals (USEPA 1993). When heated, it.

  16. Analysis of bromate in drinking water using liquid chromatography-tandem mass spectrometry without sample pretreatment.

    Science.gov (United States)

    Kosaka, Koji; Asami, Mari; Takei, Kanako; Akiba, Michihiro

    2011-01-01

    An analytical method for determining bromate in drinking water was developed using liquid chromatography-tandem mass spectrometry (LC-MS/MS). The (18)O-enriched bromate was used as an internal standard. The limit of quantification (LOQ) of bromate was 0.2 µg/L. The peak of bromate was separated from those of coexisting ions (i.e., chloride, nitrate and sulfate). The relative and absolute recoveries of bromate in two drinking water samples and in a synthesized ion solution (100 mg/L chloride, 10 mg N/L nitrate, and 100 mg/L sulfate) were 99-105 and 94-105%, respectively. Bromate concentrations in 11 drinking water samples determined by LC-MS/MS were water without sample pretreatment.

  17. Bromate formation in a hybrid ozonation-ceramic membrane filtration system.

    Science.gov (United States)

    Moslemi, Mohammadreza; Davies, Simon H; Masten, Susan J

    2011-11-01

    The effect of pH, ozone mass injection rate, initial bromide concentration, and membrane molecular weight cut off (MWCO) on bromate formation in a hybrid membrane filtration-ozonation reactor was studied. Decreasing the pH, significantly reduced bromate formation. Bromate formation increased with increasing gaseous ozone mass injection rate, due to increase in dissolved ozone concentrations. Greater initial bromide concentrations resulted in higher bromate concentrations. An increase in the bromate concentration was observed by reducing MWCO, which resulted in a concomitant increase in the retention time in the system. A model to estimate the rate of bromate formation was developed. Good correlation between the model simulation and the experimental data was achieved. Copyright © 2011 Elsevier Ltd. All rights reserved.

  18. Occurrence and sources of bromate in chlorinated tap drinking water in Metropolitan Manila, Philippines.

    Science.gov (United States)

    Genuino, Homer C; Espino, Maria Pythias B

    2012-04-01

    Significant levels of potentially carcinogenic bromate were measured in chlorinated tap drinking water in Metropolitan Manila, Philippines, using an optimized ion-chromatographic method. This method can quantify bromate in water down to 4.5 μg l⁻¹ by employing a postcolumn reaction with acidic fuchsin and subsequent spectrophotometric detection. The concentration of bromate in tap drinking water samples collected from 21 locations in cities and municipalities within the 9-month study period ranged from 7 to 138 μg l⁻¹. The average bromate concentration of all tap drinking water samples was 66 μg l⁻¹ (n = 567), almost seven times greater than the current regulatory limit in the country. The levels of bromate in other water types were also determined to identify the sources of bromate found in the distribution lines and to further uncover contaminated sites. The concentration of bromate in water sourced from two rivers and two water treatment plants ranged from 15 to 80 and 12 to 101 μg l⁻¹, respectively. Rainwater did not contribute bromate in rivers but decreased bromate level by dilution. Groundwater and wastewater samples showed bromate concentrations as high as 246 and 342 μg l⁻¹, respectively. Bromate presence in tap drinking water can be linked to pollution in natural water bodies and the practice of using hypochlorite chemicals in addition to gaseous chlorine for water disinfection. This study established the levels, occurrence, and possible sources of bromate in local drinking water supplies.

  19. [Effects of Anions on Bromate Formation During Ozonation of Bromide-Containing Water].

    Science.gov (United States)

    Wu, Yue; Wu, Chun-de; Liu, Lü-gang; Yuan, Bo-jie

    2015-09-01

    To study the effects of common inorganic anions on bromate formation during ozonation of bromide-containing water, the effects of different mass concentrations of Cl-, HCO3-, and SO(4)2- on bromate formation were investigated in bench-scale test. The mechanisms of these three coexisting anions on bromate formation was analyzed based on the ozone decomposition, HOBr/OBr- formation, and transformation of total bromine species. Our results showed that adding of 3-150 mg.L-1 Cl- can reduce 8. 8%-25. 7% of bromate formation within 60 min. 63. 9% of bromate would be decreased by increasing SO(4)2- concentration from 0 mg.L-1 to 30 mg.L-1 within 20 min. However, more than 6. 4 times the mass concentrations of bromate were formed as HCO3- mass concentrations increased from 0 mg.L-1 to 30 mg.L-1 within 20 min. The production of bromate was slightly increased when HCO3- mass concentrations was above 30 mg.L-1. Under the condition of the same ozone dosage and reaction time, adding of Cl- and SO(4)2- will inhibit the formation of bromate during ozonation, while adding of HCOC3- significantly will increase the production of bromate.

  20. Formation of bromate in sulfate radical based oxidation: mechanistic aspects and suppression by dissolved organic matter.

    Science.gov (United States)

    Lutze, Holger V; Bakkour, Rani; Kerlin, Nils; von Sonntag, Clemens; Schmidt, Torsten C

    2014-04-15

    Sulfate radical based oxidation is discussed being a potential alternative to hydroxyl radical based oxidation for pollutant control in water treatment. However, formation of undesired by-products, has hardly been addressed in the current literature, which is an issue in other oxidative processes such as bromate formation in ozonation of bromide containing water (US-EPA and EU drinking water standard of bromate: 10 μg L(-1)). Sulfate radicals react fast with bromide (k = 3.5 × 10(9) M(-1) s(-1)) which could also yield bromate as final product. The mechanism of bromate formation in aqueous solution in presence of sulfate radicals has been investigated in the present paper. Further experiments were performed in presence of humic acids and in surface water for investigating the relevance of bromate formation in context of pollutant control. The formation of bromate by sulfate radicals resembles the well described mechanism of the hydroxyl radical based bromate formation. In both cases hypobromous acid is a requisite intermediate. In presence of organic matter formation of bromate is effectively suppressed. That can be explained by formation of superoxide formed in the reaction of sulfate radicals plus aromatic moieties of organic matter, since superoxide reduces hypobromous acid yielding bromine atoms and bromide. Hence formation of bromate can be neglected in sulfate radical based oxidation at typical conditions of water treatment. Copyright © 2014. Published by Elsevier Ltd.

  1. Nitrate and bromate removal by autotrophic and heterotrophic denitrification processes: batch experiments

    National Research Council Canada - National Science Library

    Sevgi Demirel; Ibrahim Bayhan

    2013-01-01

    .... At stoichiometrically sufficient methanol concentration as an external carbon source, nitrate and bromate were reduced to below US EPA drinking water limits in heterotrophic denitrification conditions...

  2. MODELING CRYPTOSPORIDIUM PARVUM OOCYST INACTIVATION AND BROMATE IN A FLOW-THROUGH OZONE CONTACTOR TREATING NATURAL WATER

    Science.gov (United States)

    A reactive transport model was developed to simultaneously predict Cryptosporidium parvum oocyst inactivation and bromate formation during ozonation of natural water. A mechanistic model previously established to predict bromate formation in organic-free synthetic waters w...

  3. A Comparison between Ion chromatography and Inductively Coupled Plasma for the Determination of Bromate in Certain Samples of Foodstuffs

    OpenAIRE

    Alanowd O. Mehder

    2015-01-01

    Ion chromatography (IC) and inductively coupled plasma (ICP-MS) both were applied for the determination of bromate in some food samples. Attempts were made to establish calibration curves, however in case of IC, an additional abnormal peak was found to overlap with the bromate peak. This renders IC to be unsuccessful in the determination of bromate compared to ICP-MS technique. ICP-MS was found to give accurate results; therefore, it was applied for the determination of bromate in different ...

  4. Removal efficiency and economic cost comparison of hydrated electron-mediated reductive pathways for treatment of bromate

    DEFF Research Database (Denmark)

    Nawaz, Shah; Shah, Noor S.; Khan, Javed Ali

    2017-01-01

    , and different pH (highly acidic to highly basic) proved that UV-254/sulfite successfully provides aqueous electron that effectively participate in bromate removal from water. Significant removal, 86%, of initially 39.0µM bromate was achieved by UV-254/sulfite under conditions that dominate aqueous electron...... decomposition of bromate into bromide proved UV-254/sulfite-based ARPs to be economical and highly rewarding in efficient decomposition of bromate and other inorganic oxyhalides....

  5. Determination of BROMATE AT PARTS-PER-TRILLION LEVELS BY GAS CHROMATOGRAPHY-MASS SPECTROMETRY WITH NEGATIVE CHEMICAL IONIZATION

    Science.gov (United States)

    The ozonation of bromide-containing source waters produces bromate as a class 2B carcinogenic disinfection by-product. The present work describes the determination of bromate by gas chromatography-negative chemical ionization mass spectrometry (GC-NCIMS) following a bromate react...

  6. Potassium Bromate Assay by Redox Titrimetry Using Arsenic Trioxide.

    Science.gov (United States)

    Smeller, Johanna M; Leigh, Stefan D

    2003-01-01

    Bromate, a disinfectant, is one of the analytes of interest in wastewater analysis. Environmental laboratories have a regulatory need for their measurements to be traceable to NIST standards. Bromate is not currently certified as a NIST Standard Reference Material (SRM). Therefore, a traceable assay of potassium bromate (KBrO3) is needed. KBrO3 was dissolved in water and assayed by redox titrimetry using arsenic trioxide (As2O3). A nominal (0.1 g) sample of As2O3 was dissolved in 10 mL of 5 mol/L sodium hydroxide. The solution was acidified with hydrochloric acid and about 95 % of the KBrO3 titrant was added gravimetrically. The end point was determined by addition of dilute (1:3) titrant using an automated titrator. The KBrO3 assay was determined to be 99.76 % ± 0.20 %. The expanded uncertainty considered the titrations of three independently prepared KBrO3 solutions.

  7. Revisiting the Kinetics and Mechanism of Bromate-Bromide Reaction

    Directory of Open Access Journals (Sweden)

    Côrtes Carlos Eduardo S.

    2001-01-01

    Full Text Available The bromate-bromide reaction was investigated in an acidity range not studied yet. The reaction was followed at the Br2/Br3- isosbestic point (lambda = 446 nm. It was observed a first-order behavior for bromate and bromide ions and a second-order behavior for H+ ion that results in the rate law nu = k[BrO3-][Br- ][H+]². This rate law suggests a mechanism involving two successive protonation of bromate followed by the interaction of the intermediate species H2BrO3+ with bromide. These results disagree with the obtained by other authors who observed a second-order behavior for the bromide and first-order for H+, and have proposed intermediate species like H2Br2O3 and HBr2O3-. The second-order for [H+] observed in the range 0.005 <= [H+] <= 2.77 mol L-1 sets down that the pKa of bromic acid, HBrO3, must be lower than -0.5 (T = 25 °C, different from all other values for this pKa proposed in the literature.

  8. Bromate formation in bromide-containing water through the cobalt-mediated activation of peroxymonosulfate.

    Science.gov (United States)

    Li, Zhaobing; Chen, Zhi; Xiang, Yingying; Ling, Li; Fang, Jingyun; Shang, Chii; Dionysiou, Dionysios D

    2015-10-15

    Bromate formation in bromide-containing water through the cobalt (Co)-mediated activation of peroxymonosulfate (PMS) was investigated. Increasing the PMS dosage and the cobalt dosage increased the formation of bromate and bromate yields of up to 100% were recorded under the test conditions. The bromate yield increased to a maximum as the pH rose from 2.7 to 6 before decreasing by over 90% as the pH rose further from 6 to above 9. The bromate formation is a two-step process involving free bromine as a key intermediate and bromate as the final product. In the first step, apart from the known oxidation of bromide to free bromine and of free bromine to bromate by sulfate radicals (SO4(-)), Co(III) produced from the oxidation of Co(II) by PMS and SO4(-) also oxidizes bromide to free bromine. The contribution of Co(III) to the bromate formation was verified with the addition of methanol and EDTA, a radical scavenger and a Co(III) ligand, respectively. In the presence of methanol, free bromine formation increased with increasing Co(II) dosage but no bromate was detected, indicating that Co(III) oxidized bromide to form free bromine but not bromate. In the presence of both EDTA and methanol, no free bromine or bromate was detected, as Co(III) was stabilized by EDTA to form the Co(III)EDTA(-) complex, which could not oxidize bromide. Mathematical simulation further suggested that Co(III) outweighed SO4(-) to oxidize bromide to free bromine. On the other hand, SO4(-) is essential for the oxidation of free bromine to bromate in the second step. In real water, the presence of NOM significantly decreased the bromate formation but caused the brominated organic DBP formation with high quantity. This is the first study to demonstrate the significant bromate formation in the Co/PMS system and the substantial contribution of Co(III) to the formation. Copyright © 2015 Elsevier Ltd. All rights reserved.

  9. Performance of sodium bromate as cathodic electron acceptor in microbial fuel cell.

    Science.gov (United States)

    Dai, Hongyan; Yang, Huimin; Liu, Xian; Zhao, Yu; Liang, Zhenhai

    2016-02-01

    The potential of using sodium bromate as a cathodic electron acceptor in a microbial fuel cell (MFC) was determined in this study. The effects of sodium bromate concentration and initial catholyte pH on the electricity production of the MFC were investigated. The MFC performance improved with increasing sodium bromate concentration and decreasing catholyte pH. The maximum voltage output (0.538 V), power density (1.4908 W m(-3)), optimal open circuit potential (1.635 V), coulombic efficiency (11.1%), exchange current density (0.538 A m(-3)) and charge transfer resistance (4274.1 Ω) were obtained at pH 3.0 and 100 mM sodium bromate. This work is the first to confirm that sodium bromate could be used as an electron acceptor in MFCs. Copyright © 2015 Elsevier Ltd. All rights reserved.

  10. Pilot study on bromate reduction in ozonation of water with low carbonate alkalinities by carbon dioxide.

    Science.gov (United States)

    Li, Ji; Zou, Li; Guo, Lulu; Ji, Jialin

    2011-01-01

    A pilot study was carried out to explore the application of carbon dioxide for pH depression in a bubble column and its ability to inhibit bromate formation for water with a low alkalinity. Results showed that in the absence of ammonia, CO2 was capable of reducing bromate 38.0%-65.4% with one-unit pH depression. CO2 caused a slightly lower bromate reduction (4.2%) than did H2SO4 when the pH was depressed to 7.4, and a more a pronounced lower reduction (8.8%) when the pH was depressed to 6.9. In the presence of 0.20 mg/L-N ammonia, bromate was largely inhibited with 73.9% reduction. When the pH was depressed to 7.4, CO2 and H2SO4 showed an 11.3% and 23.5% bromate reduction respectively, demonstrating that the joint use of CO2 and ammonia might be a plausible strategy of blocking all three bromate formation pathways. CO2 could be applied through the aeration diffuser together with ozone gas, resulting in a similar bromate reduction compared with the premixing method through Venturi mixer.

  11. Acute kidney injury due to sodium bromate intoxication: a report of two cases.

    Science.gov (United States)

    Ryu, Dong Hwan; Jang, Kyung Ae; Kim, Seok Min; Park, Jong Won; Do, Jun Young; Yoon, Kyung Woo

    2011-12-01

    Sodium bromate is a strong oxidant used as a neutralizing solution in hair permanents, as well as an auxiliary agent in printing and dyeing. Accidental or deliberate ingestion of bromate solution has rarely been reported in Korea. The clinical manifestations of bromate intoxication are vomiting, diarrhea, central nervous system symptoms, oliguric or non-oliguric acute kidney injury, hemolytic anemia, and deafness; most of these manifestations are reversible, with the exception of renal failure and deafness. Here, we report on two patients who demonstrated distinct clinical progressions. In the first case, a 16-year-old woman was successfully treated with hemodialysis and recovered renal function without hearing loss. However, in the second case, delayed hemodialysis resulted in persistent renal failure and hearing loss in a 77-year-old woman. This suggests that emergency therapeutic measures, including hemodialysis, should be taken as soon as possible, as the rapid removal of bromate may be essential to preventing severe intoxication and its sequelae.

  12. Complex spatiotemporal behavior in the photosensitive ferroin-bromate-4-nitrophenol reaction.

    Science.gov (United States)

    Bell, Jeffrey G; Wang, Jichang

    2015-04-09

    Investigation illustrates that the bromate-4-nitrophenol reaction in a stirred batch reactor undergoes spontaneous oscillations under very broad initial reactant concentrations. The addition of ferroin has subtle influences on the nonlinear behavior, in which the frequency and total number of oscillations were greatly reduced at a low or high ferroin concentration, as opposed to the significant increase at a moderate ferroin concentration. Temporal oscillations with a modulating frequency were also observed in the ferroin-bromate-4-nitrophenol system. In a capillary tube the ferroin-bromate-4-nitrophenol reaction generated propagating wave trains with various complex behaviors such as period-doubled intermittent propagation failure. Illumination was found to have a profound effect on the temporal oscillations in the bromate-4-nitrophenol reaction and on those long lasting wave activities. Spectroscopic studies were able to identify 1,4-benzoquinone, 2-bromo-1,4-benzoquinone, and 2-bromo-4-nitrophenol as major components during the reaction.

  13. Determination of bromate in drinking water by ultraperformance liquid chromatography-tandem mass spectrometry.

    Science.gov (United States)

    Alsohaimi, Ibrahim Hotan; Alothman, Zeid Abdullah; Khan, Mohammad Rizwan; Abdalla, Mohammad Abulhassan; Busquets, Rosa; Alomary, Ahmad Khodran

    2012-10-01

    Bromate is a byproduct formed as a result of disinfection of bromide-containing source water with ozone or hypochlorite. The International Agency for Research on Cancer has recognized bromate as a possible human carcinogen, thus it is essential to determine in drinking water. Present work highlights a development of sensitive and fast analytical method for bromate determination in drinking water by using ultraperformance liquid chromatography-tandem mass spectrometry. The quality parameters of the developed method were established, obtaining very low limit of detection (0.01 ng/mL), repeatability and reproducibility have been found to be less than 3% in terms of relative standard deviation when analyzing a bromate standard at 0.05 μg/mL with 0.4 min analysis time. Developed method was applied for the analysis of metropolitan and bottled water from Saudi Arabia; 22 samples have been analyzed. Bromate was detected in the metropolitan water samples (from desalinization source) at concentrations ranging between 3.43 and 75.04 ng/mL and in the bottled water samples at concentrations ranging between 2.07 and 21.90 ng/mL. Moreover, in comparison to established analytical methods such as liquid chromatography-tandem mass spectrometry, the proposed method was found to be very sensitive, selective and rapid for the routine analysis of bromate at low level in drinking water. © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  14. [Determination of trace bromate in drinking water by ion chromatography with suppressed conductivity detection].

    Science.gov (United States)

    Ying, Bo; Li, Shumin; Yue, Yinling; Xueli, E

    2006-05-01

    Bromate is a common disinfection by-product produced from the ozonation of source water containing bromide. An ion exchange chromatographic method with suppressed conductivity detection for the determination of trace bromate in drinking water was developed. The separation of the bromate in drinking water was achieved on a Metrosep A Supp 5 anion exchange column and a Metrosep A Supp 4/5 Guard column with a carbonate eluent. A new dual suppressed system, an MSM II chemical suppressor combined with a CO2 suppressor, was used to suppress the background conductivity, and to improve the detection limit of bromate. Ion chromatographic experiments were carried out by using a Metrosep A Supp 5 anion exchange column with a suppressed conductivity detector and an eluent of 3.2 mmoL/L Na2CO3-1.0 mmol/L NaHCO3 at a flow rate of 0.65 mL/min. This method had good linearity (r = 0.9999) in the range of 5-100 microg/L and high precision (relative standard deviation (RSD) water, pure water and mineral water were 96.1%-107%, and the detection limit for bromate was 0.50 microg/L. This method has a simple operation procedure, good separation results, high sensitivity and good repeatability. It can be used as a standard method for the determination of bromate in drinking water.

  15. Room temperature phosphorimetric determination of bromate in flour based on energy transfer.

    Science.gov (United States)

    Menendez-Miranda, Mario; Fernandez-Argüelles, Maria T; Costa-Fernandez, Jose M; Pereiro, Rosario; Sanz-Medel, Alfredo

    2013-11-15

    Determination of bromate ions in contaminated flour samples by using a room temperature phosphorescence (RTP) optosensor is described. The optosensor is based on the non-radiative energy transfer from α-bromonaphthalene (a phosphorescent molecule insensitive to the presence of the analyte) acting as donor, to an energy acceptor bromate-sensitive molecule (trifluoperazine hydrochloride). The RTP emission of the selected donor greatly overlaps with the absorption spectrum of the acceptor, resulting in a decrease of the measured signal as the concentration of bromate ions increases. A simple and general procedure is proposed to carry out the incorporation of both the donor and acceptor molecules in an appropriate solid material (sensing phase) through the co-immobilization of the species in a sol-gel inorganic matrix. The optimum amounts of the sol-gel precursors, including silica precursors, type of catalysis, and concentrations of donor and acceptor molecules, have been evaluated in order to obtain the best analytical features of the proposed optosensor for bromate determination. The highly stable developed sensing phase shows a selective and reversible response towards bromate even in presence of dissolved oxygen (a well-known quencher of the RTP). The calibration graphs were linear up to 200 mg L(-1), with a detection limit for bromate dissolved in aqueous medium of 0.2 mg L(-1). Sample throughput of the proposed optosensor was about 18 measurements h(-1). Application of the developed sensing phase was successfully proved for the detection of bromate ions in commercial flours, obtaining good recoveries. © 2013 Elsevier B.V. All rights reserved.

  16. Bromide oxidation by ferrate(VI): The formation of active bromine and bromate.

    Science.gov (United States)

    Jiang, Yanjun; Goodwill, Joseph E; Tobiason, John E; Reckhow, David A

    2016-06-01

    Ferrate (VI) (abbreviated as Fe(VI)) has long been considered as a green oxidant that does not produce any known hazardous byproducts. However, this work shows that Fe(VI) can slowly oxidize bromide forming active bromine (HOBr/OBr(-)) and bromate, and in natural waters total organic bromine (TOBr) can also be detected. Results showed that the highest levels of active bromine and bromate were formed at lower pHs and in the absence of phosphate. Hydrogen peroxide, which forms from the reaction of Fe(VI) and water, plays an essential role in suppressing bromate formation by reducing active bromine back to bromide. Fe(VI) decomposition products (assumed to be particulate phase Fe(III)) can catalyze the decomposition of hydrogen peroxide by Fe(VI). Phosphate had a substantial inhibiting effect on the formation of active bromine, but less so on bromate formation. The presence of the raw water matrix in natural water suppressed bromate formation. For a natural water spiked with 0.1 mg/L of bromide, the bromate and TOBr concentrations after Fe(VI) oxidation were below 3.0 and 15 μg/L, respectively. No consistent trend regarding the effect of pH or buffer ions on TOBr formation was observed due to the competition between Fe(VI), hydrogen peroxide, and natural organic matter (NOM) for reaction with active bromine. Under environmentally relevant conditions, the formation of bromate and TOBr would not be a problem for Fe(VI) application as their concentration levels are quite low. Copyright © 2016 Elsevier Ltd. All rights reserved.

  17. Determination of bromate in sea water using multi-dimensional matrix-elimination ion chromatography.

    Science.gov (United States)

    Zakaria, Philip; Bloomfield, Carrie; Shellie, Robert A; Haddad, Paul R; Dicinoski, Greg W

    2011-12-16

    A multi-dimensional matrix-elimination ion chromatography approach has been applied to the determination of bromate in seawater samples. Two-dimensional and three-dimensional configurations were evaluated for their efficacy to eliminate the interference caused by the high concentration of ubiquitous ions present in seawater, such as chloride and sulfate. A two-dimensional approach utilising a high capacity second dimension separation comprising two Dionex AS24 columns connected in series was applied successfully and permitted the determination of bromate in undiluted seawater samples injected directly onto the ion chromatography system. Using this approach the limit of detection (LOD) for bromate based on a signal to noise ratio of 3 was 1050 μg/L using a 500 μL injection loop. Good linearity was obtained for bromate with correlation coefficients for the calibration curves of 0.9981 and 0.9996 based on peak height and area, respectively. A three-dimensional method utilising two 10-port switching valves to allow sharing of the second suppressor and detector between the second and third dimension separations showed better resolution and detection for bromate and reduced the LOD to 60 μg/L for spiked seawater samples. Good linearity was maintained with correlation coefficients of 0.9991 for both peak height and area. Ozonated seawater samples were also analysed and exhibited a non-linear increase in bromate level on increasing ozonation time. A bromate concentration in excess of 1770 μg/L was observed following ozonation of the seawater sample for 120 min. Recoveries for the three-dimensional system were 92% and 89% based on peak height and area, respectively, taken over 5 ozonated samples with 3 replicates per sample. Copyright © 2011 Elsevier B.V. All rights reserved.

  18. Reducing bromate formation with H(+)-form high silica zeolites during ozonation of bromide-containing water: Effectiveness and mechanisms.

    Science.gov (United States)

    Zhang, Tao; Hou, Pin; Qiang, Zhimin; Lu, Xiaowei; Wang, Qunhui

    2011-01-01

    This paper investigated the effect of H(+)-form high silica ZSM-5 (HZSM-5) zeolites on bromate formation. HZSM-5 zeolites with different Si/Al molar ratios (i.e., 25-300) were tested taking ozonation alone as control. The zeolites were more effective in reducing bromate formation for the filtered surface water than CeO₂, a former reported oxide that can reduce bromate formation at slightly acidic pH. The reduction efficiencies were not closely related to their Si/Al ratios. The HZSM-5 (Si/Al=300) selected for detailed studies effectively reduced bromate formation by 58% for the filtered water, and also enhanced the removal of dissolved organic carbon (DOC) during ozonation. The efficiency of the HZSM-5 in reducing bromate formation increased with ozone dose (0.38-1.16 mg O₃ mg⁻¹ DOC) and pH (6.6-9.3). The HZSM-5 adsorbed OBr⁻ (one of the critical intermediates in bromate formation) quickly with an adsorption capacity of 54 mg g⁻¹, but had no adsorption for ozone, Br⁻, HOBr and BrO₃⁻. It also significantly inhibited the formation of trace H₂O₂ which was generated from ozone decomposition and had been considered promoting bromate formation at low concentrations during ozonation. The reduction of bromate formation in O₃/HZSM-5 is possibly ascribed to the selective OBr⁻ adsorption in combination with the inhibited H₂O₂ formation. Copyright © 2010 Elsevier Ltd. All rights reserved.

  19. [Simultaneous determination of bromate and perchlorate in vegetable by ion chromatography tandem mass spectrometry].

    Science.gov (United States)

    Yang, Jiajia; Yang, Yi; Zhang, Jing; Shao, Bing; Wu, Yongning

    2012-03-01

    To develop a method for simultaneous determination of bromate and perchiorate in vegetable using ion chromatography tandem mass spectrometry. Target ions in vegetable matrix were extracted by water and purified using a GCB cartridge. With the hydrophilic Ion Pac AS19 column and linear gradient potassium hydroxide used as eluent, bromate and perchlorate were analyzed by a triple quadrupole mass spectrometer under negative electronspray ionization mode and multiple reaction monitoring (MRM). Internal standard calibration was used for quantification. Good linearity was achieved for bromate and perchlorate over the range of 0.1- 50 microg/L and 0.05-50 microg/L, respectively, with correlation coefficients R2 > 0.998. The quantification limits of the method were 2.5 microg/kg and 0.7 microg/kg for bromate and perchlorate, respectively. Mean recoveries of two target analytes (spiked at three concentration levels in 5 kinds of vegetables) ranged from 80.3% to 124%, with within-day precisions no more than 21.4% and intraday precisions no more than 12.2%. This method could be applied in the simultaneous detection of bromate and perchlorate in vegetable.

  20. Bromate pollutant in ozonated bottled Zamzam water from Saudi Arabia determined by LC/ICP-MS.

    Science.gov (United States)

    Al-Ansi, Seham A; Othman, Ahmed A; Al-Tufail, Mohammed A

    2011-01-01

    Bromate (BrO(3) (-)) as a human carcinogenic pollutant in bottled drinking Zamzam water from Mecca, Saudi Arabia has been determined using liquid chromatography inductively coupled plasma mass spectrometry (LC/ICP-MS). For analysis, samples were injected directly without any further pretreatment, using only 50 μL injection volume. The method showed: 0.5 μg/L detection limit, 1.0 μg/L limit of quantification and 1.0-200.0 μg/L linearity range (r(2) = 0.9998). The relative standard deviation (%RSD) values for reproducibility (interday precision) obtained are at 11 % and 14 % for bromate and bromide at low concentration levels (5, 10 μg/L) and at 4 % for both at high concentration levels (50, 100 μg/L), respectively. The results concluded that the ozonated bottled Zamzam water samples are contaminated with bromate. The concentration is 20 times higher than U.S. Environmental Protection Agency (U.S. EPA) allowable limit (10 μg/L) for bromate in bottled drinking water. Bottled drinking water brands, disinfected with ozone showed relatively lower levels of bromate as compared with Zamzam water.

  1. Fe(II)-Al(III) layered double hydroxides prepared by ultrasound-assisted co-precipitation method for the reduction of bromate.

    Science.gov (United States)

    Zhong, Yu; Yang, Qi; Luo, Kun; Wu, Xiuqiong; Li, Xiaoming; Liu, Yang; Tang, Wangwang; Zeng, Guangming; Peng, Bo

    2013-04-15

    Bromate is recognized as an oxyhalide disinfection byproduct in drinking water. In this paper, Fe(II)-Al(III) layered double hydroxides (Fe-Al LDHs) prepared by the ultrasound-assisted co-precipitation method were used for the reduction of bromate in solution. The Fe-Al LDHs particles were characterized by X-ray diffractometer, scanning electron microscopy and thermogravimetry-differential scanning calorimetry. It was found that ultrasound irradiation assistance promoted the formation of the hydrotalcite-like phase and then improved the removal efficiency of bromate. In addition, the effects of solid-to-solution ratio, contact time, initial bromate concentration, initial pH, coexisting anions on the bromate removal were investigated. The results showed the bromate with an initial concentration of 1.56 μmol/L could be completely removed from solution by Fe-Al LDHs within 120 min. When the initial bromate concentration was 7.81 μmol/L, the Fe-Al LDHs with irradiation time of 30 min exhibited the optimum removal efficiency and the bromate removal capacity (qe) was 6.80 μmol/g. In addition, the appearance of sulfate and production of bromide were observed simultaneously in this process, which suggested that ion-exchange between sulfate and bromate, and the reduction of bromate to bromide by Fe(2+) were the main mechanisms responsible for the bromate removal by Fe-Al LDHs. Copyright © 2013 Elsevier B.V. All rights reserved.

  2. Determination of bromate in water samples using post column derivatization method with triiodide.

    Science.gov (United States)

    Michalski, Rajmund; Lyko, Aleksandra

    2010-08-01

    This paper describes the application of the method of post-column derivatization with triiodide and UV detection at 352 nm for the determination of bromate in drinking water, mineral water and swimming pool water samples. Optimized analytical conditions were further validated in terms of accuracy, precision, linearity, limit of detection and limit of quantification. The method detection limit was at the level of 0.4 μg/L, and the spiked recovery for bromate was in the range of 92% - 104%. The method did not need a special sample treatment and was successfully applied to the analysis of bromate at the required value that is below 2.5 μg/L.

  3. Bromate peak distortion in ion chromatography in samples containing high chloride concentrations.

    Science.gov (United States)

    Pappoe, Michael K; Naeeni, Mohammad Hosein; Lucy, Charles A

    2016-04-29

    In this study, the effect of column overload of the matrix ion, chloride, on the elution peak profiles of trace bromate is investigated. The resultant peak profiles of chloride and bromate are explained on the basis of competitive Langmuir isotherms. The Thermo IonPac AS9-HC, AS19 and AS23 columns are recommended by the manufacturer for bromate (a carcinogen) analysis. Under trace conditions, these columns provide baseline resolution of bromate from matrix ions such as chloride (Rs=2.9, 3.3 and 3.2, respectively for the three columns). Injection of 10-300 mM chloride with both hydroxide and carbonate eluents resulted in overload on these columns. On the basis of competitive Langmuir isotherms, a deficiency in the local concentration of the more retained eluent in addition to analyte overload leads to fronting of the overloaded analyte peak. The peak asymmetries (B/A10%) for chloride changed from 1.0 (Gaussian) under trace conditions to 0.7 (fronting) at 300 mM Cl(-) for IonPac AS9-HC, 0.9-0.6 for AS19 and 0.8-0.5, for AS23, respectively. The 10mM bromate peak is initially near Gaussian (B/A10%=0.9) but becomes increasingly distorted and pulled back into the chloride peak as the concentration of chloride increased. Increasing the eluent strength reduced the pull-back effect on bromate and fronting in chloride in all cases. Copyright © 2016 Elsevier B.V. All rights reserved.

  4. Bromate Formation Characteristics of UV Irradiation, Hydrogen Peroxide Addition, Ozonation, and Their Combination Processes

    Directory of Open Access Journals (Sweden)

    Naoyuki Kishimoto

    2012-01-01

    Full Text Available Bromate formation characteristics of six-physicochemical oxidation processes, UV irradiation, single addition of hydrogen peroxide, ozonation, UV irradiation with hydrogen peroxide addition (UV/H2O2, ozonation with hydrogen peroxide addition (O3/H2O2, and ozonation with UV irradiation (O3/UV were investigated using 1.88 μM of potassium bromide solution with or without 6.4 μM of 4-chlorobenzoic acid. Bromate was not detected during UV irradiation, single addition of H2O2, and UV/H2O2, whereas ozone-based treatments produced . Hydroxyl radicals played more important role in bromate formation than molecular ozone. Acidification and addition of radical scavengers such as 4-chlorobenzoic acid were effective in inhibiting bromate formation during the ozone-based treatments because of inhibition of hydroxyl radical generation and consumption of hydroxyl radicals, respectively. The H2O2 addition was unable to decompose 4-chlorobenzoic acid, though O3/UV and O3/H2O2 showed the rapid degradation, and UV irradiation and UV/H2O2 showed the slow degradation. Consequently, if the concentration of organic contaminants is low, the UV irradiation and/or UV/H2O2 are applicable to organic contaminants removal without bromate formation. However, if the concentration of organic contaminants is high, O3/H2O2 and O3/UV should be discussed as advanced oxidation processes because of their high organic removal efficiency and low bromate formation potential at the optimum condition.

  5. Propagation failures, breathing fronts, and nonannihilation collisions in the ferroin-bromate-pyrocatechol system

    Science.gov (United States)

    Harati, Mohammad; Wang, Jichang

    2009-06-01

    The emergence of propagating pulses was investigated with the photosensitive ferroin-bromate-pyrocatechol reaction in capillary tubes, in which various interesting spatiotemporal behaviors such as propagation failure, breathing fronts, and transitions between propagating pulses and fronts have been observed. Rather than a mutual annihilation, the collision of a propagating pulse and a growing front forces the front to recede gradually. A phase diagram in the pyrocatechol-bromate concentration space shows that the pulse instabilities take place throughout the conditions at which the system generates wave activities, suggesting that the presence of coupled autocatalytic feedbacks may facilitate the onset of pulse instabilities.

  6. Effect of characteristics of activated carbon on removal of bromate

    Energy Technology Data Exchange (ETDEWEB)

    Huang, W.J.; Cheng, Y.L. [Hung Kuang University, Taichung (Taiwan). Dept. of Environmental Engineering

    2008-02-15

    This study evaluates how the characteristics of activated carbon (AC) influence the adsorption-reduction of bromate (BrO{sup 3-}) by performing kinetic and isotherm tests. Experimental results reveal that both physical and chemical effects simultaneously affect the adsorption-reduction process. The wood-based carbons contained more mesopores than coconut- and coal-based carbons, resulting in the adsorption of more BrO{sup 3-}. The equilibrium- and maximum-adsorption capacities were calculated as a function of the effect of mesopore volume. The carbon surface chemistry seems to be significant in the adsorption-reduction process. Activated carbons with high pH(zpc) values and many basic groups exhibit a neutral or positive charge under typical pH conditions, promoting BrO{sup 3-} adsorption-reduction at the carbon surface. The kinetic data obtained from three forms of carbons have been analyzed using three kinetic models-pseudo-first-order, pseudo-second-order and intraparticle diffusion models. Among the kinetic models studied, the intraparticle diffusion was the best applicable model to describe the adsorption of BrO{sup 3-} onto AC.

  7. Subchronic toxicity evaluation of potassium bromate in Fischer 344 rats.

    Science.gov (United States)

    Dodd, Darol E; Layko, Debra K; Cantwell, Katherine E; Willson, Gabrielle A; Thomas, Russell S

    2013-11-01

    Male F344 rats were exposed to potassium bromate (KBrO₃) in drinking water at concentrations of 0, 5, 20, 100, 200, or 400 mg/L for 2 or 13 weeks. Endpoints evaluated included clinical observations, body weights, serum chemistry, gross pathology, organ weights, and select tissue histopathology (kidney, lung, liver, thyroid, and tunica vaginalis). Weekly body weight and water consumption means were similar between KBrO₃ and control groups throughout the study. Increases in kidney weights were observed in rats of the 400 mg/L group following 2- or 13-weeks exposure. Hyaline droplets were observed in renal tubules of rats of the 200 and 400 mg/L groups following 2 weeks exposure and in rats of the 400 mg/L group at 13 weeks. There were no KBrO₃-related microscopic findings in the lung, liver, thyroid, and tunica vaginalis at the 2- and 13-week time points. A no observed effect level of 100 mg/L KBrO₃ (8.1 mg/kg/day) was selected based on the absence of microscopic alterations in the kidney. Copyright © 2013 Elsevier B.V. All rights reserved.

  8. Fe(II)–Al(III) layered double hydroxides prepared by ultrasound-assisted co-precipitation method for the reduction of bromate

    Energy Technology Data Exchange (ETDEWEB)

    Zhong, Yu [College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China); Key Laboratory of Environmental Biology and Pollution Control, Hunan University, Ministry of Education, Changsha 410082 (China); Yang, Qi, E-mail: yangqi@hnu.edu.cn [College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China); Key Laboratory of Environmental Biology and Pollution Control, Hunan University, Ministry of Education, Changsha 410082 (China); Luo, Kun; Wu, Xiuqiong [College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China); Key Laboratory of Environmental Biology and Pollution Control, Hunan University, Ministry of Education, Changsha 410082 (China); Li, Xiaoming, E-mail: xmli@hnu.edu.cn [College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China); Key Laboratory of Environmental Biology and Pollution Control, Hunan University, Ministry of Education, Changsha 410082 (China); Liu, Yang [College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China); Urban and Rural Garbage Disposal Technology Research Center, Hunan Province, Changsha 410082 (China); Tang, Wangwang; Zeng, Guangming; Peng, Bo [College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China); Key Laboratory of Environmental Biology and Pollution Control, Hunan University, Ministry of Education, Changsha 410082 (China)

    2013-04-15

    Highlights: ► Fe(II)–Al(III) LDHs were synthesized by ultrasound-assisted co-precipitation method. ► The Fe–Al (30 min) exhibited highly reduction reactivity on bromate. ► Pseudo-first-order model described the experimental data well. ► The mechanisms of bromate removal were proposed. -- Abstract: Bromate is recognized as an oxyhalide disinfection byproduct in drinking water. In this paper, Fe(II)–Al(III) layered double hydroxides (Fe–Al LDHs) prepared by the ultrasound-assisted co-precipitation method were used for the reduction of bromate in solution. The Fe–Al LDHs particles were characterized by X-ray diffractometer, scanning electron microscopy and thermogravimetry–differential scanning calorimetry. It was found that ultrasound irradiation assistance promoted the formation of the hydrotalcite-like phase and then improved the removal efficiency of bromate. In addition, the effects of solid-to-solution ratio, contact time, initial bromate concentration, initial pH, coexisting anions on the bromate removal were investigated. The results showed the bromate with an initial concentration of 1.56 μmol/L could be completely removed from solution by Fe–Al LDHs within 120 min. When the initial bromate concentration was 7.81 μmol/L, the Fe–Al LDHs with irradiation time of 30 min exhibited the optimum removal efficiency and the bromate removal capacity (q{sub e}) was 6.80 μmol/g. In addition, the appearance of sulfate and production of bromide were observed simultaneously in this process, which suggested that ion-exchange between sulfate and bromate, and the reduction of bromate to bromide by Fe{sup 2+} were the main mechanisms responsible for the bromate removal by Fe–Al LDHs.

  9. Conversion of organic micropollutants with limited bromate formation during the Peroxone process in drinking water treatment

    NARCIS (Netherlands)

    Knol, A.H.; Lekkerkerker-Teunissen, K.; Houtman, C.J.; Scheideler, J.; Ried, A.; Van Dijk, J.C.

    2015-01-01

    Advanced oxidation with O3 / H2O2 (peroxone) was conducted on pilot plant scale on pre-treated Meuse river water to investigate the conversion of organic micropollutants (OMPs) and the formation of bromate. Fourteen selected model compounds were dosed to the pre-treated river water on a regular

  10. Surface studies on as-grown (111) faces of sodium bromate crystals

    Indian Academy of Sciences (India)

    Unknown

    Abstract. Single crystals of sodium bromate are grown at various supersaturations ranging from 3% to 8%. Surface studies have been carried out on as-grown and etched (111) faces of these crystals. Typical and syste- matically oriented growth hillocks are observed almost on all the faces. Further dislocation studies are ...

  11. MUTATIONS IN THE VHL GENE FRIOM POTASSIUM BROMATE-INDUCED RAT CLEAR CELL RENAL TUMORS

    Science.gov (United States)

    Potassium bromate (KBrO3) is a rat renal carcinogen and a major drinking water disinfection by-product in water disinfected with ozone. Clear cell renal tumors, the most common form of human renal epithelial neoplasm, are rare in animals but are inducible by KBrO3 in F344 rats. ...

  12. Study On Adsorption of Bromate From Aqueous Solution On Modified Activated Carbon

    Science.gov (United States)

    Liu, Tong-mian; Cui, Fu-yi; Zhao, Zhi-wei; Liu, Dong-mei; Zhu, Qi; Wang, Huan

    2010-11-01

    A coal-based activated carbon was treated chemically with nitric acid, sodium hydroxide and ammonia for its surface modification, and its adsorption capacity was investigated with bromate. Several techniques were used to characterize the physicochemical properties of these materials including BET, XPS, pHpzc and Boehm titration. The results indicated that the specific surface area of the activated carbon decreased after oxidation with nitric acid. But the amount of surface acidic oxygen-containing functional groups of the oxidized sample increased compared to the raw carbon and the points of zero charge (pHpzc) decreased. The specific surface area of the activated carbon also decreased after sodium hydroxide treatment and the points of zero charge increased. The changes of surface chemical properties after the ammonia treatment was opposite to the oxidized sample. As a result, the pHpzc of the carbon was increased to near pH9.3, the amount of surface basic groups was increased. Furthermore, the data of bromate adsorption on all the samples were fitted to the Langmuir isotherm model well which indicates monolayer adsorption. In addition, the adsorption capacity of ammonia treatment sample was the highest and its saturated adsorption capacity reached 1.55 mg/g. A strong correlation was found between basic groups and adsorption capacity of bromate. Enhancement of basic groups was favorable for bromate removal.

  13. On the failure of sustained oscillations in the bromate/hypophosphite-acetone/dual catalyst flow system

    Science.gov (United States)

    Nogueira, Paulo A.; Faria, Roberto B.; Varela, Hamilton

    2013-02-01

    In this report we present experimental results on the dynamical behavior of the bromate/hypophosphite-acetone/dual catalyst system. According to our findings we state that this two-catalyst system does not show oscillations under flow conditions. Our discussion is based on the sequential action of the two catalysts system.

  14. Determination of Bromate at Trace Level in Sudanese Bottled Drinking Water Using Ion Chromatography

    Directory of Open Access Journals (Sweden)

    Mei Musa

    2010-01-01

    Full Text Available Bromate ion was determined by ion chromatography with spectro-photometric detection after post column reaction with o-dianisidine reagent in acidic medium. IonPac AS19 anion-exchange column was used with 20 mM sodium hydroxide eluent. The eluent from the column was then allowed to react with o-dianisidine at 60 °C. The developed colour of the final product was measured spectrophotometrically at 450 nm. Linearity of the method was checked up to 200 μg/L by using 200 μL sample injection volume and the linear correlation coefficient was 0.9998. The method detection limit was 0.56 μg/L and the precision was 6.2% at 100 μg/L. The spiked recovery for bromate in water samples was 93%. Interferences from some anions eg. nitrate, chloride and nitrite were studied. The method was applied for the determination of bromate ion in ten sudanese bottled drinking water. Bromate was detected in 60% of the samples at concentrations ranged between 5-169 μg/L.

  15. KIDNEY TOXICOGENOMICS OF ACUTE SODIUM AND POTASSIUM BROMATE EXPOSURE IN F344 MALE RAT

    Science.gov (United States)

    Bromate, used in both the food and cosmetics industry, is a drinking water disinfection by-product that is nephrotoxic and carcinogenic to rodents. To gain insight into the carcinogenic mechanism of action, identify possible biomarkers of exposure, and determine if the cation, po...

  16. KIDNEY TOXICOGENOMICS OF CHRONIC POTASSIUM BROMATE EXPOSURE IN F344 MALE RAT

    Science.gov (United States)

    Potassium bromate (KBrO3), used in both the food and cosmetics industry, and a drinking water disinfection by-product, is a nephrotoxic compound and rodent carcinogen. To gain insight into the carcinogenic mechanism of action and provide possible biomarkers of KBrO3 exposure, the...

  17. Determination of dissolved bromate in drinking water by ion chromatography and post column reaction: interlaboratory study.

    Science.gov (United States)

    Cordeiro, Fernando; Robouch, Piotr; de la Calle, Maria Beatriz; Emteborg, Håkan; Charoud-Got, Jean; Schmitz, Franz

    2011-01-01

    A collaborative study, International Evaluation Measurement Programme-25a, was conducted in accordance with international protocols to determine the performance characteristics of an analytical method for the determination of dissolved bromate in drinking water. The method should fulfill the analytical requirements of Council Directive 98/83/EC (referred to in this work as the Drinking Water Directive; DWD). The new draft standard method under investigation is based on ion chromatography followed by post-column reaction and UV detection. The collaborating laboratories used the Draft International Organization for Standardization (ISO)/Draft International Standard (DIS) 11206 document. The existing standard method (ISO 15061:2001) is based on ion chromatography using suppressed conductivity detection, in which a preconcentration step may be required for the determination of bromate concentrations as low as 3 to 5 microg/L. The new method includes a dilution step that reduces the matrix effects, thus allowing the determination of bromate concentrations down to 0.5 microg/L. Furthermore, the method aims to minimize any potential interference of chlorite ions. The collaborative study investigated different types of drinking water, such as soft, hard, and mineral water. Other types of water, such as raw water (untreated), swimming pool water, a blank (named river water), and a bromate standard solution, were included as test samples. All test matrixes except the swimming pool water were spiked with high-purity potassium bromate to obtain bromate concentrations ranging from 1.67 to 10.0 microg/L. Swimming pool water was not spiked, as this water was incurred with bromate. Test samples were dispatched to 17 laboratories from nine different countries. Sixteen participants reported results. The repeatability RSD (RSD(r)) ranged from 1.2 to 4.1%, while the reproducibility RSD (RSDR) ranged from 2.3 to 5.9%. These precision characteristics compare favorably with those of ISO

  18. A new catalytic oxidation method for sensitive quantification of bromate in flours and bottled water using AgNPs.

    Science.gov (United States)

    Farmany, Abbas; Mortazavi, Seyede Shima; Hashemi, Ehsan; Sahraei, Reza

    2014-03-01

    In this paper, a simple and sensitive spectrophotometric method for the determination of nanomolar level of bromate, based on the catalytic effect of silver nanoparticles on the oxidation of acid red 14 by potassium bromate, is described. The reaction rate was monitored spectrophotometrically by measuring the decrease in absorbance of acid red 14 at 516 nm. The detection limit of the method was 8 ng/mL, and the linear range was between 15 and 130 ng/mL. The effects of acidity, concentration of reactants and reaction time, and external ions were also discussed. The optimum reaction conditions were fixed, and some kinetic parameters determined. The relative standard deviation for the determination of bromate at the concentration of 50 ng/mL was calculated to be 0.996 % (n = 10). The method has been successfully applied to the determination of bromate in flours and bottled waters.

  19. CONSUMER WILLINGNESS TO PAY FOR SAFETY LABELS IN NIGERIA: A CASE STUDY OF POTASSIUM BROMATE IN BREAD

    Directory of Open Access Journals (Sweden)

    O Oni

    2006-05-01

    Full Text Available The study analysed consumer willingness to pay for safety labels in Nigeria by a case study of potassium bromate in bread” in Benin City, Edo State. It specifi cally investigates factors that promote willingness to pay for label among consumers of bread in Benin City, Edo State. Data used for the study were obtained through a well-structured questionnaire from 200 respondents. Both descriptive analytical methods and probit regression models were used for the analysis. The study revealed that 73% of the respondents are in their active working age with 50 percent of the respondent being male and female respectively. 67 percent of the respondents are married with 55 percent having an average of 5 members per household. 99 percent of the respondents are educated i.e. they have the capability of being able to read and write. Respondents purchased bread mainly from hawkers (60% with about 60% of them being aware of the presence of bromate in bread. 40% of the consumers used labeling as a way of identifying bromate free bread. Other methods reported deal with differences in price of bread with same weight, aroma and taste. Result also revealed that 60% of the respondents got to know about the negative effect of bromate from news (both print and mass media. Econometric results show that variables like education, gender, income, prior knowledge of bromate and perception held by respondents of negative implications of bromate signifi cantly infl uence the willingness to pay for safety labels. Education, gender, income and prior knowledge of bromate positively infl uence the probability of consumers’ decision to pay for safety label, while price of bread and confi dence and perception held by respondents of negative implications of bromate on human health infl uence consumers willingness to pay more for safety labels. The study, thus, suggests a defi ned market for bread purchases, community based awareness programme and extension of National Agency

  20. Enhancement of bromate formation by pH depression during ozonation of bromide-containing water in the presence of hydroxylamine.

    Science.gov (United States)

    Yang, Jingxin; Li, Ji; Dong, Wenyi; Ma, Jun; Yang, Yi; Li, Jiayin; Yang, Zhichao; Zhang, Xiaolei; Gu, Jia; Xie, Wanying; Cang, Yan

    2017-02-01

    This work investigated the fate of bromate formation during ozonation in the presence of hydroxylamine (HA). Results indicated that pH depression, as a commonly feasible control strategy for bromate formation during ozonation, unexpectedly enhanced the bromate formation during ozonation in the presence of HA. A dramatically high level of bromate was observed at acidic pH in the ozone/HA process. The scavenging experiments demonstrated the essential role of OH produced in the reaction of ozone with HA in bromate formation. In the process, OH mainly oxidizes bromide to Br, which is further oxidized by ozone and eventually converts to bromate. Further investigations suggested that the unexpected enhancement on bromate formation by pH depression can be mainly ascribed to the pH-dependent ozone decay, OH exposures and formation rate of Br. As pH decreased from 7 to 5, the reduced OH scavenging capacity of HA led to higher OH exposures, which contributed to the enhancement of bromate formation. As pH decreased from 5 to 3, the enhanced formation rate of Br largely augmented the formation of bromate. In addition, the ozone decay slowed down by pH depression provided more available ozone for the oxidation of the formed Br to bromate. The enhanced effect of pH depression on bromate formation was still observed in the real water samples in the ozone/HA process. Accordingly, pH depression might be avoided to control the bromate formation during ozonation in the presence of HA. Copyright © 2016 Elsevier Ltd. All rights reserved.

  1. Advanced oxidation of bromide-containing drinking water: a balance between bromate and trihalomethane formation control.

    Science.gov (United States)

    Wang, Yongjing; Yu, Jianwei; Han, Po; Sha, Jing; An, Tao; Li, Wei; Liu, Juan; Yang, Min

    2013-11-01

    Addition of H202 has been employed to repress bromate formation during ozonation of bromide-containing source water. However, the addition of H2O2 will change the oxidation pathways of organic compounds due to the generation of abundant hydroxyl radicals, which could affect the removal efficacy of trihalomethane precursors via the combination of ozone and biological activated carbon (O3-BAC). In this study, we evaluated the effects of H2O2 addition on bromate formation and trihalomethane formation potential (THMFP) reduction during treatment of bromide-containing (97.6-129.1 microg/L) source water by the O3-BAC process. At an ozone dose of 4.2 mg/L, an H2O2/O3 (g/g) ratio of over 1.0 was required to maintain the bromate concentration below 10.0 microg/L, while a much lower H2O2/O3 ratio was sufficient for a lower ozone dose. An H2O2/O3 (g/g) ratio below 0.3 should be avoided since the bromate concentration will increase with increasing H2O2 dose below this ratio. However, the addition of H202 at an ozone dose of 3.2 mg/L and an H2O2/O3 ratio of 1.0 resulted in a 43% decrease in THMFP removal when comparedwith the O3-BAC process. The optimum H2O2/O3 (g/g) ratio for balancing bromate and trihalomethane control was about 0.7-1.0. Fractionation of organic materials showed that the addition of H2O2 decreased the removal efficacy of the hydrophilic matter fraction of DOC by ozonation and increased the reactivity of the hydrophobic fractions during formation of trihalomethane, which may be the two main reasons responsible for the decrease in THMFP reduction efficacy. Overall, this study clearly demonstrated that it is necessary to balance bromate reduction and THMFP control when adopting an H2O2 addition strategy.

  2. Complete bromate and nitrate reduction using hydrogen as the sole electron donor in a rotating biofilm-electrode reactor

    Energy Technology Data Exchange (ETDEWEB)

    Zhong, Yu; Li, Xin [College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China); Key Laboratory of Environmental Biology and Pollution Control, Hunan University, Ministry of Education, Changsha 410082 (China); Yang, Qi, E-mail: yangqi@hnu.edu.cn [College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China); Key Laboratory of Environmental Biology and Pollution Control, Hunan University, Ministry of Education, Changsha 410082 (China); Wang, Dongbo [College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China); Key Laboratory of Environmental Biology and Pollution Control, Hunan University, Ministry of Education, Changsha 410082 (China); Advanced Water Management Centre, The University of Queensland, QLD 4072 (Australia); Yao, Fubing [College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China); Key Laboratory of Environmental Biology and Pollution Control, Hunan University, Ministry of Education, Changsha 410082 (China); Li, Xiaoming, E-mail: xmli@hnu.edu.cn [College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China); Key Laboratory of Environmental Biology and Pollution Control, Hunan University, Ministry of Education, Changsha 410082 (China); Zhao, Jianwei; Xu, Qiuxiang; Zhang, Chang; Zeng, Guangming [College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China); Key Laboratory of Environmental Biology and Pollution Control, Hunan University, Ministry of Education, Changsha 410082 (China)

    2016-04-15

    Graphical abstract: Main mechanism of simultaneous bromate and nitrate removal in the RBER. - Highlights: • Cathode of RBER was designed to automatically rotate. • Simultaneous bromate and nitrate removal was achieved by auto-hydrogenotrophic reduction. • The maximum bromate reduction rate estimated by the Monod equation was 109.12 μg/L h. • An electron transfer process and main reaction mechanism in RBER was explored. - Abstract: Simultaneous reduction of bromate and nitrate was investigated using a rotating biofilm-electrode reactor (RBER) with graphite carbon (GC) rods as anode and activated carbon fiber (ACF) bonded with steel ring as cathode. In RBER, the community of denitrifying bacteria immobilized on the cathode surface could completely utilize hydrogen (H{sub 2}) as the electron donor, which was internally produced by the electrolysis of water. The short-term test confirmed that the RBER system could reduce 150–800 μg/L bromate to below 10 μg/L under autotrophic conditions. The reduced bromate was considered to be roughly equivalent to the amount of bromide in effluent, indicating that bromate was completely reduced to bromide without accumulation of by-products. The long-term test (over 120 days) showed that the removal fluxes of bromate and nitrate could be improved by increasing the electric current and decreasing the hydraulic retention time (HRT). But nitrite in effluent was significantly accumulated when the electric current was beyond 10 mA and the HRT was less than 6 h. The maximum bromate reduction rate estimated by the Monod equation was 109.12 μg/L h when the electric current was 10 mA and HRT was 12 h. It was proposed that the electron transfer process in RBER produced H{sub 2} on the surface of the ACF cathode, and the microbial cultures attached closely on the cathode which could completely utilize H{sub 2} as electron donors for reduction of bromate and nitrate.

  3. Complete bromate and nitrate reduction using hydrogen as the sole electron donor in a rotating biofilm-electrode reactor.

    Science.gov (United States)

    Zhong, Yu; Li, Xin; Yang, Qi; Wang, Dongbo; Yao, Fubing; Li, Xiaoming; Zhao, Jianwei; Xu, Qiuxiang; Zhang, Chang; Zeng, Guangming

    2016-04-15

    Simultaneous reduction of bromate and nitrate was investigated using a rotating biofilm-electrode reactor (RBER) with graphite carbon (GC) rods as anode and activated carbon fiber (ACF) bonded with steel ring as cathode. In RBER, the community of denitrifying bacteria immobilized on the cathode surface could completely utilize hydrogen (H2) as the electron donor, which was internally produced by the electrolysis of water. The short-term test confirmed that the RBER system could reduce 150-800μg/L bromate to below 10μg/L under autotrophic conditions. The reduced bromate was considered to be roughly equivalent to the amount of bromide in effluent, indicating that bromate was completely reduced to bromide without accumulation of by-products. The long-term test (over 120 days) showed that the removal fluxes of bromate and nitrate could be improved by increasing the electric current and decreasing the hydraulic retention time (HRT). But nitrite in effluent was significantly accumulated when the electric current was beyond 10mA and the HRT was less than 6h. The maximum bromate reduction rate estimated by the Monod equation was 109.12μg/Lh when the electric current was 10mA and HRT was 12h. It was proposed that the electron transfer process in RBER produced H2 on the surface of the ACF cathode, and the microbial cultures attached closely on the cathode which could completely utilize H2 as electron donors for reduction of bromate and nitrate. Copyright © 2015 Elsevier B.V. All rights reserved.

  4. Bromate catalytic reduction in continuous mode using metal catalysts supported on monoliths coated with carbon nanofibers

    OpenAIRE

    Marco, Yanila; Garcia-Bordeje, Enrique; Franch, Cristina; Palomares, Antonio E.; Yuranova, Tatiana; Kiwi-Minsker, Lioubov

    2013-01-01

    Nitrogen-doped and un-doped carbon nanofibers layers, denoted as N-CNFs and CNFs respectively, coating the walls of cordierite monoliths have been used as support for Pd and Ru catalyst. They have been tested in bromate reduction in batch and continuous operation employing different reactor configurations. The CNF/monolith catalysts were benchmarked with Pd catalyst on CNF coated on another structured support, namely sintered metal fibers. CNF/monolith is a robust, active and stable catalyst ...

  5. Titrimetric and spectrophotometric determination of doxycycline hyclate using bromate-bromide, methyl orange and indigo carmine

    Directory of Open Access Journals (Sweden)

    Pavagada Jagannathamurthy Ramesh

    2010-07-01

    Full Text Available One titrimetric and two indirect spectrophotometric methods are described for the determination of doxycycline hyclate (DCH in bulk drug and in its formulations. The methods use bromate-bromide, methyl orange and indigo carmine as reagents. In titrimetry (method A, DCH is treated with a known excess of bromate- -bromide mixture in acid medium and the residual bromine is back titrated iodometrically after the reaction between DCH and in situ bromine is ensured to be complete. In spectrophotometric methods, the excess of bromine is estimated by treating with a fixed amount of either methyl orange (method B or indigo carmine (method C and measuring the change in absorbance either at 520 or 610 nm. Titrimetric method is applicable over 1-8 mg range and the calculations are based on a 1:2 (DCH:bromate stoichiometric ratio. In spectrophotometry, the calibration graphs were found to be linear over 0.25-1.25 and 1.0-5.0 μg mL-1 for method B and C, respectively, with corresponding molar absorptivity values of 2.62×105 and 6.97×104 L mol-1 cm-1. The accuracy and precision of the assays were determined by computing the intra-day and inter-day variations at three different levels of DCH.

  6. Ruthenium catalyst on carbon nanofiber support layers for use in silicon-based structured microreactors, Part II: Catalytic reduction of bromate contaminants in aqueous phase

    NARCIS (Netherlands)

    Thakur, D.B.; Tiggelaar, Roald M.; Weber, Y.; Gardeniers, Johannes G.E.; Lefferts, Leonardus; Seshan, Kulathuiyer

    2011-01-01

    Catalyst layers were synthesized inside a structured channel of silicon based microreactor and used to remove bromate contaminants in water. It is demonstrated that Ru/CNF based catalyst is active for bromate reduction, resulting in turn over frequencies (TOFs) higher than conventional powdered

  7. Modeling Cryptosporidium parvum oocyst inactivation and bromate in a flow-through ozone contactor treating natural water.

    Science.gov (United States)

    Kim, Jae-Hong; Elovitz, Michael S; von Gunten, Urs; Shukairy, Hiba M; Mariñas, Benito J

    2007-01-01

    A reactive transport model was developed to simultaneously predict Cryptosporidium parvum oocyst inactivation and bromate formation during ozonation of natural water. A mechanistic model previously established to predict bromate formation in organic-free synthetic waters was coupled with an empirical ozone decay model and a one-dimensional axial dispersion reactor (ADR) model to represent the performance of a lab-scale flow-through ozone bubble-diffuser contactor. Dissolved ozone concentration, bromate concentration (in flow-through experiments only), hydroxyl radical exposure and C. parvum oocyst survival were measured in batch and flow-through experiments performed with filtered Ohio River water. The model successfully represented ozone concentration and C. parvum oocyst survival ratio in the flow-through reactor using parameters independently determined from batch and semi-batch experiments. Discrepancies between model prediction and experimental data for hydroxyl radical concentration and bromate formation were attributed to unaccounted for reactions, particularly those involving natural organic matter, hydrogen peroxide and carbonate radicals. Model simulations including some of these reactions resulted in closer agreement between predictions and experimental observations for bromate formation.

  8. Bromate and trace metal levels in bread loaves from outlets within Ile-Ife Metropolis, Southwestern Nigeria

    Directory of Open Access Journals (Sweden)

    J.A.O. Oyekunle

    2014-01-01

    Full Text Available Bread loaves randomly sampled from nine outlets and bakeries within Ile-Ife were analysed to determine their safety levels for human consumption with respect to bromate and trace metal contents. Bromate determination was carried out via spectrophotometric method while trace metals in the digested bread samples were profiled using Flame Atomic Absorption Spectrophotometer. Bromate levels in the analyzed bread samples ranged from 2.051 ± 0.011 μg/g to 66.224 ± 0.014 μg/g while the trace metal levels were of the order: 0.03–0.10 μg/g Co = 0.03–0.10 μg/g Pb < 0.23–0.46 μg/g Cu < 2.23–6.63 μg/g Zn < 25.83–75.53 μg/g Mn. This study revealed that many bread bakers around Ile-Ife had not fully complied with the bromate-free rule stipulated by NAFDAC contrary to the “bromate free” inscribed on the labels of the bread. The bread samples contained both essential and toxic trace metals to levels that could threaten the health of consumers over prolonged regular consumption.

  9. Sensitive determination of bromate in ozonated and chlorinated water, and sea water by gas chromatography-mass spectrometry after derivatization.

    Science.gov (United States)

    Shin, Ho-Sang

    2012-02-03

    A sensitive gas chromatographic method has been established for the determination of bromate in ozonated and chlorinated water, and in sea water. With acidic conditions, bromate reacts with chloride to form bromine, which reacts with 2,6-dialkylphenol to form 4-bromo-2,6-dialkylphenol. The organic derivative was extracted with ethyl acetate after quenching remaining oxidants with ascorbic acid, and then measured by gas chromatography-mass spectrometry (GC-MS). The lowest detection limit and limit of quantification of bromate in drinking water were 0.02 and 0.07 μg/L, respectively, and the calibration curve showed good linearity with r²=0.998. The 32 common ions did not interfere even when present in 100-fold excess over the bromated ion. The accuracy was in a range of 102-106% and the precision of the assay was less than 6% in chlorinated and ozonated tap water, ozonated mineral water, and sea water. The method was sensitive, reproducible and simple enough to permit reliable analysis of bromate to the ng/L level in water. Copyright © 2011 Elsevier B.V. All rights reserved.

  10. Oxidation of micro or trace amounts of bromide to bromate by peroxodisulphate before their iodometric determination by titration or spectrophotometry.

    Science.gov (United States)

    Lundström, U

    1982-04-01

    The optimum conditions for the oxidation of bromide to bromate by peroxodisulphate at 120 degrees as well as for the decomposition of the excess of oxidant have been determined. The predicted advantages of this oxidizing agent, viz. minimal blanks and destruction of small amounts of interfering organic matter and reducing substances, were confirmed. The bromate was determined iodometrically either by titration with thiosulphate or by spectrophotometry in absence of oxygen at 355 nm. The titrimetric finish applied to 0.8-8 micromole of bromide gave a mean yield of 100.0%, s = 6 nmole. The spectrophotometric finish applied to 0.05-0.25 micromole of bromide gave a mean yield of 98.9%, s = 1.1 nmole. Interfering amounts of iodide present in the sample and oxidized to iodate can be corrected for by making use of the pH-dependence of the reaction of iodide with bromate and iodate.

  11. Pathway fraction of bromate formation during O₃ and O₃/H₂O₂ processes in drinking water treatment.

    Science.gov (United States)

    Qi, Shengqi; Mao, Yuqin; Lv, Miao; Sun, Lili; Wang, Xiaomao; Yang, Hongwei; Xie, Yuefeng F

    2016-02-01

    Ozone process has been widely used for drinking water treatment recently. In the oxidation process, bromate is formed by three pathways, i.e., the direct pathway, the direct-indirect pathway and the indirect-direct pathway. This study developed a method to calculate the percentage of these three pathways for bromate formation during O3 process and O3/H2O2 process. Two kinds of water, distilled water containing bromide (DW) and surface water from the Yellow River (SW) were selected as raw rater. The result showed that in natural water systems, the direct-indirect pathway was dominant for bromate formation during the oxidation process. When 3 mg L(-1) O3 was used as the only oxidant, nearly 26% of bromide ion was transferred into bromate in two kinds of water after 80 min. The dominant pathway in DW was the direct pathway (48.5%) and the direct-indirect pathway (46.5%), while that was the direct-indirect pathway (68.9%) in SW. When O3/H2O2 were used as oxidants, as the H2O2 dosage increased, the fractions of bromate formation by direct pathway and direct-indirect pathway decreased, while that by indirect-direct pathway increased. The conversion ratio from bromide to bromate first kept stable or increased, then decreased and reached its minimum when [H2O2]/[O3] ratio was 1.0 in DW and 1.5 in SW. Under this condition the indirect-direct pathway took the largest fraction of 70.7% in DW and 64.0% in SW, respectively. Copyright © 2015. Published by Elsevier Ltd.

  12. A mineral and antioxidant-rich extract from the red marine Algae Alsidium corallinum exhibits cytoprotective effects against potassium bromate-induced erythrocyte oxidative damages in mice.

    Science.gov (United States)

    Ben Saad, Hajer; Nasri, Imen; Elwej, Awatef; Krayem, Najeh; Jarraya, Raoudha; Kallel, Choumous; Zeghal, Najiba; Amara, Ibtissem Ben

    2014-07-01

    The present study was carried out to investigate potassium bromate toxicity in mice and the corrective effects of marine algae Alsidium corallinum. The red algae demonstrated its rich composition in phenols, triterpenes, flavonoids, alkaloids, tropolones, sodium, potassium, calcium, magnesium, iron, copper, and zinc. To confirm its antioxidant potential, an in vivo study was performed on adult mice. The animals were divided into four groups: group I were used as controls, group II received potassium bromate (0.5 g/L) via drinking water, group III received potassium bromate (0.5 g/L) by the same route as group II and 7% of A. corallinum ethanolic extract via their diet, and group IV received only 7% of algae. The potassium bromate-treated group showed a significant decrease in erythrocyte, platelet, hemoglobin, and hematocrit values and a significant increase in total white blood cells, compared to those of controls. While, superoxide dismutase, catalase, glutathione, and vitamin C values were decreased by potassium bromate treatment, lipid peroxidation (as malondialdehyde) and erythrocyte osmotic fragility values were increased. Interestingly, potassium bromate treatment showed significant genotoxic effects, as demonstrated by DNA degradation. These changes were confirmed by blood smears histopathological observations which were marked by a necrosis and a decrease of erythrocytes number. A. corallinum extract appeared to be effective against hematotoxic and genotoxic changes induced by potassium bromate, as evidenced by the improvement of the parameters cited above.

  13. Chlorination of bromide-containing waters: enhanced bromate formation in the presence of synthetic metal oxides and deposits formed in drinking water distribution systems.

    Science.gov (United States)

    Liu, Chao; von Gunten, Urs; Croué, Jean-Philippe

    2013-09-15

    Bromate formation from the reaction between chlorine and bromide in homogeneous solution is a slow process. The present study investigated metal oxides enhanced bromate formation during chlorination of bromide-containing waters. Selected metal oxides enhanced the decay of hypobromous acid (HOBr), a requisite intermediate during the oxidation of bromide to bromate, via (i) disproportionation to bromate in the presence of nickel oxide (NiO) and cupric oxide (CuO), (ii) oxidation of a metal to a higher valence state in the presence of cuprous oxide (Cu2O) and (iii) oxygen formation by NiO and CuO. Goethite (α-FeOOH) did not enhance either of these pathways. Non-charged species of metal oxides seem to be responsible for the catalytic disproportionation which shows its highest rate in the pH range near the pKa of HOBr. Due to the ability to catalyze HOBr disproportionation, bromate was formed during chlorination of bromide-containing waters in the presence of CuO and NiO, whereas no bromate was detected in the presence of Cu2O and α-FeOOH for analogous conditions. The inhibition ability of coexisting anions on bromate formation at pH 8.6 follows the sequence of phosphate > sulfate > bicarbonate/carbonate. A black deposit in a water pipe harvested from a drinking water distribution system exerted significant residual oxidant decay and bromate formation during chlorination of bromide-containing waters. Energy dispersive spectroscopy (EDS) analyses showed that the black deposit contained copper (14%, atomic percentage) and nickel (1.8%, atomic percentage). Cupric oxide was further confirmed by X-ray diffraction (XRD). These results indicate that bromate formation may be of concern during chlorination of bromide-containing waters in distribution systems containing CuO and/or NiO. Copyright © 2013 Elsevier Ltd. All rights reserved.

  14. Chlorination of bromide-containing waters: Enhanced bromate formation in the presence ofsynthetic metal oxides and deposits formed indrinking water distribution systems

    KAUST Repository

    Liu, Chao

    2013-09-01

    Bromate formation from the reaction between chlorine and bromide in homogeneous solution is a slow process. The present study investigated metal oxides enhanced bromate formation during chlorination of bromide-containing waters. Selected metal oxides enhanced the decay of hypobromous acid (HOBr), a requisite intermediate during the oxidation of bromide to bromate, via (i) disproportionation to bromate in the presence of nickel oxide (NiO) and cupric oxide (CuO), (ii) oxidation of a metal to a higher valence state in the presence of cuprous oxide (Cu2O) and (iii) oxygen formation by NiO and CuO. Goethite (α-FeOOH) did not enhance either of these pathways. Non-charged species of metal oxides seem to be responsible for the catalytic disproportionation which shows its highest rate in the pH range near the pKa of HOBr. Due to the ability to catalyze HOBr disproportionation, bromate was formed during chlorination of bromide-containing waters in the presence of CuO and NiO, whereas no bromate was detected in the presence of Cu2O and α-FeOOH for analogous conditions. The inhibition ability of coexisting anions on bromate formation at pH 8.6 follows the sequence of phosphate>>sulfate>bicarbonate/carbonate. A black deposit in a water pipe harvested from a drinking water distribution system exerted significant residual oxidant decay and bromate formation during chlorination of bromide-containing waters. Energy dispersive spectroscopy (EDS) analyses showed that the black deposit contained copper (14%, atomic percentage) and nickel (1.8%, atomic percentage). Cupric oxide was further confirmed by X-ray diffraction (XRD). These results indicate that bromate formation may be of concern during chlorination of bromide-containing waters in distribution systems containing CuO and/or NiO. © 2013 Elsevier Ltd.

  15. Dynamics of bromate oscillators with 1,4-cyclohexanedione in a continuously fed stirred tank reactor

    Science.gov (United States)

    Keresztúri, Klára; Szalai, István

    2006-09-01

    The dynamics of the bromate-1,4-cyclohexanedione reaction and its ferroin catalyzed version in a continuously fed stirred tank reactor are reported. In the ([Br -] 0, [H 2SO 4] 0) and ([Br -] 0, [ferroin] 0) planes steady-state bistability and oscillations are observed. Close to the upper [Br -] 0 limit of the oscillatory domain the oscillations become aperiodic. By increasing the [ferroin] 0 the characteristic of the oscillations switches from 'uncatalyzed' to 'catalyzed'-type. Additionally, the effects of the bromide ions and ferroin on the batch dynamics are investigated.

  16. Photo-mediated bromate--1,4-benzoquinone reaction: A novel photochemical oscillator

    Science.gov (United States)

    Zhao, Bei; Wang, Jichang

    2006-10-01

    1,4-Benzoquinone is uncovered to react with acidic bromate in the presence of illumination, in which temporal oscillations are observed in the stirred batch system. This new photochemical oscillator shows subtle dependence on compositions of the reaction mixture, in which oscillations could be revived immediately upon the addition of fresh 1,4-benzoquinone solution. A proposed mechanism on the basis of light-induced conversion of 1,4-benzoquinone to 1,4-hydroquinone qualitatively reproduces the oscillatory phenomena as well as the long induction time seen in experiments.

  17. Addition of hydrogen peroxide for the simultaneous control of bromate and odor during advanced drinking water treatment using ozone.

    Science.gov (United States)

    Wang, Yongjing; Yu, Jianwei; Zhang, Dong; Yang, Min

    2014-03-01

    Complete removal of the characteristic septic/swampy odor from Huangpu River source water could only be achieved under an ozone dose as high as 4.0 mg/L in an ozone-biological activated carbon (O3-BAC) process, which would lead to the production of high concentrations of carcinogenic bromate due to the high bromide content. This study investigated the possibility of simultaneous control of bromate and the septic/swampy odor by adding H2O2 prior to the O3-BAC process for the treatment of Huangpu River water. H2O2 addition could reduce the bromate concentration effectively at an H2O2/O3 (g/g) ratio of 0.5 or higher. At the same time, the septic/swampy odor removal was enhanced by the addition of H2O2, although optimization of the H2O2/O3 ratio was required for each ozone dose. At an ozone dose of 2.0 mg/L, the odor was removed completely at an H2O2/O3 ratio of 0.5. The results indicated that H2O2 application at a suitable dose could enhance the removal of the septic/swampy odor while suppressing the formation of bromate during ozonation of Huangpu River source water. Copyright © 2014 The Research Centre for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.

  18. USE OF qRTPCR TO IDENTIFY POTENTIAL BIOMARKERS OF BROMATE EXPOSURE IN F344 MALE RAT KIDNEYS

    Science.gov (United States)

    Potassium bromate (KBrO3) is a drinking water disinfection by-product that is nephrotoxic and carcinogenic. To identify potential biomarkers of carcinogenicity, male F344 rats were chronically exposed to a carcinogenic dose (400mg/l) of KBrO3 in their drinking water. Kidneys were...

  19. Mixed mode and sequential oscillations in the cerium-bromate-4-aminophenol photoreaction

    Energy Technology Data Exchange (ETDEWEB)

    Bell, Jeffrey G.; Wang Jichang [Department of Chemistry and Biochemistry, University of Windsor, Windsor, Ontario N9B 3P4 (Canada)

    2013-09-15

    Cerium was introduced to the bromate-aminophenol photochemical oscillator to implement coupled autocatalytic feedbacks. Mixed mode and sequential oscillations emerged in the studied system, making it one of the few chemical oscillators known to support consecutive bifurcations in a batch system. The complex reaction behavior showed a strong dependence on the intensity of illumination supplied to the system. Removal of illumination during an oscillatory window affected both the frequency and amplitude of the oscillation but did not fully extinguish them, indicating that the cerium-bromate-4-aminophenol oscillator was photosensitive rather than photo-controlled. A moderate light intensity allowed for a slow evolution of the system, which proved to be critical for the emergence of transient complex oscillations. Variation of individual reaction parameters was carried out, which indicated that the development of complex oscillations occur in a narrow region and a phase diagram in the 4-aminophenol and sulfuric acid plane demonstrated this. Simulations provide strong support that transient complex oscillations observed experimentally arise from the coupling of two autocatalytic cycles.

  20. Comparison of the oxidation of two porphyrin complexes by bromate with respect to wave propagation

    Science.gov (United States)

    Rácz, Krisztina; Burger, Maria; Ungvarai-Nagy, Zsuzsanna

    2010-06-01

    The kinetics and mechanism of the oxidation of iron(III) protoporphyrin IX (hemin) and iron(III) meso-tetra(4-sulfonatophenyl)porphine (TPPSFe) were compared. Both reactions exhibit sigmoid-shaped time dependence of the absorbance of the porphyrin complexes during the course of the reaction. The oxidation of hemin was proved to be an autocatalytic reaction resembling very much the autocatalytic subset reaction of the BZ oscillators. The oxidation of TPPSFe was proved not to be autocatalytic. It consists of consecutive reaction steps without any feedback. One of the intermediates absorbing in the same region as TPPSFe could be identified as an iron(V)-oxo complex of TPPS. According to the kinetic differences, single autocatalytic wave fronts could be observed in the autocatalytic hemin-bromate reaction if hemin was fixed and stabilized in silica gels, while no wave formation appeared in the TPPSFe-bromate system. The kinetic differences are in agreement with the different structures of the two porphyrin complexes.

  1. An electrochemiluminescence sensor for bromate assay based on a new cationic polythiophene derivative.

    Science.gov (United States)

    Li, Xiaojian; Li, Jianxiu; Wang, Huan; Li, Rongxia; Ma, Hongmin; Du, Bin; Wei, Qin

    2014-12-10

    A sensitive electrochemiluminescence (ECL) sensor was fabricated for bromate assay based on a cationic polythiophene derivative, poly[3-(1,1'-dimethyl-4-piperidinemethylene)thiophene-2,5-diyl chloride] (PTh-D)/nafion modified Au electrode. Bromate was used as the coreactant as well as detecting analyte in the ECL sensor for the first time. The prepared PTh-D exhibited excellent solubility, strong and stable cathodic ECL activity. PTh-D can be immobilized on the surface of Au electrode via AuS bonding and nafion and chitosan were also used to immobilize PTh-D. The fabricated sensor exhibited a good linear relationship between the ECL intensities and the concentrations of BrO3(-) ranging from 1 μM to 0.1 M with a detection limit of 1 μM. This proposed method not only expands the application of PTh-D, but also opens new doors toward the detection of BrO3(-). Copyright © 2014 Elsevier B.V. All rights reserved.

  2. Spectrophotometric determination of nitrite by its catalytic effect on the oxidation of congo red with bromate

    Directory of Open Access Journals (Sweden)

    Zenovia Moldovan

    2012-08-01

    Full Text Available A novel simple, sensitive and rapid kinetic-spectrophotometric method for the determination of trace amounts of nitrite is proposed. The method is based on its catalytic effect on the oxidation of congo red (CR by potassium bromate in acidic solution. The oxidation reaction is monitored spectrophotometrically by measuring the decrease in the absorbance of CR at a suitable λmax = 570 nm for the first 10–40 s from the start of the reaction. Under the optimum experimental conditions (sulfuric acid, 0.3 M; CR, 0.75Χ10-4 M; potassium bromate, 5Χ10-4 M and 25 oC, nitrite can be determined in the range of 0.015–0.75 µg mL−1 with the detection limit of 0.006 µg mL−1. The relative standard deviation of five replicate determination of 0.25 µg mL−1 nitrite was 2.5%. The proposed method was applied satisfactorily to the determination of nitrite in spiked drinking water samples.DOI: http://dx.doi.org/10.4314/bcse.v26i2.1

  3. Nigella sativa fixed and essential oil modulates glutathione redox enzymes in potassium bromate induced oxidative stress.

    Science.gov (United States)

    Sultan, Muhammad Tauseef; Butt, Masood Sadiq; Karim, Roselina; Ahmed, Waqas; Kaka, Ubedullah; Ahmad, Shakeel; Dewanjee, Saikat; Jaafar, Hawa Z E; Zia-Ul-Haq, M

    2015-09-18

    Nigella sativa is an important component of several traditional herbal preparations in various countries. It finds its applications in improving overall health and boosting immunity. The current study evaluated the role of fixed and essential oil of Nigella sativa against potassium bromate induced oxidative stress with special reference to modulation of glutathione redox enzymes and myeloperoxidase. Animals; 30 rats (Sprague Dawley) were divided in three groups and oxidative stress was induced using mild dose of potassium bromate. The groups were on their respective diets (iso-caloric diets for a period of 56 days) i.e. control and two experimental diets containing N. sativa fixed (4%) and essential (0.3%) oils. The activities of enzymes involved in glutathione redox system and myeloperoxidase (MPO) were analyzed. The experimental diets modulated the activities of enzymes i.e. glutathione-S-transferase (GST), glutathione reductase (GR) and glutathione peroxidase (GPx) positively. Indices of antioxidant status like tocopherols and glutathione were in linear relationship with that of GPx, GR and GST (Pbromate induced oxidative stress.

  4. Mixed mode and sequential oscillations in the cerium-bromate-4-aminophenol photoreaction

    Science.gov (United States)

    Bell, Jeffrey G.; Wang, Jichang

    2013-09-01

    Cerium was introduced to the bromate-aminophenol photochemical oscillator to implement coupled autocatalytic feedbacks. Mixed mode and sequential oscillations emerged in the studied system, making it one of the few chemical oscillators known to support consecutive bifurcations in a batch system. The complex reaction behavior showed a strong dependence on the intensity of illumination supplied to the system. Removal of illumination during an oscillatory window affected both the frequency and amplitude of the oscillation but did not fully extinguish them, indicating that the cerium-bromate-4-aminophenol oscillator was photosensitive rather than photo-controlled. A moderate light intensity allowed for a slow evolution of the system, which proved to be critical for the emergence of transient complex oscillations. Variation of individual reaction parameters was carried out, which indicated that the development of complex oscillations occur in a narrow region and a phase diagram in the 4-aminophenol and sulfuric acid plane demonstrated this. Simulations provide strong support that transient complex oscillations observed experimentally arise from the coupling of two autocatalytic cycles.

  5. Ion Chromatographic Method with Post-Column Fuchsin Reaction for Measurement of Bromate in Chlorinated Water

    Directory of Open Access Journals (Sweden)

    Homer C. Genuino

    2009-06-01

    Full Text Available An ion chromatographic method that employs a post-column reaction with fuchsin and spectrophotometric detection was optimized for measuring bromate (BrO3- in water. BrO3- is converted to Br2 by sodium metabisulfite and then reacted with acidic fuchsin to form a red-colored product that strongly absorbs at 530 nm. The reaction of BrO3- and fuchsin reagent is optimum at pH 3.5 and 65 oC. The method has a limit of quantitation of 4.5 µg L-1 and is linear up to 150 µg L-1 BrO3-. Recoveries from spiked samples were high ranging from 95 to 102 % using external standard calibration and 87 to 103 % using standard addition method. Intra-batch and inter-batch reproducibility studies of the method resulted to RSD values ranging from 0.62 to 2.01 % and percent relative error of 0.12 to 2.94 % for BrO3- concentrations of 10 µg L-1 and 50 µg L-1. This method is free of interferences from common inorganic anions at levels typically found in chlorinated tap drinking water without preconcentration. The optimized method can be applied to trace analysis of bromate in chlorinated tap drinking water samples.

  6. Simultaneous detection of perchlorate and bromate using rapid high-performance ion exchange chromatography-tandem mass spectrometry and perchlorate removal in drinking water.

    Science.gov (United States)

    West, Danielle M; Mu, Ruipu; Gamagedara, Sanjeewa; Ma, Yinfa; Adams, Craig; Eichholz, Todd; Burken, Joel G; Shi, Honglan

    2015-06-01

    Perchlorate and bromate occurrence in drinking water causes health concerns due to their effects on thyroid function and carcinogenicity, respectively. The purpose of this study was threefold: (1) to advance a sensitive method for simultaneous rapid detection of perchlorate and bromate in drinking water system, (2) to systematically study the occurrence of these two contaminants in Missouri drinking water treatment systems, and (3) to examine effective sorbents for minimizing perchlorate in drinking water. A rapid high-performance ion exchange chromatography-tandem mass spectrometry (HPIC-MS/MS) method was advanced for simultaneous detection of perchlorate and bromate in drinking water. The HPIC-MS/MS method was rapid, required no preconcentration of the water samples, and had detection limits for perchlorate and bromate of 0.04 and 0.01 μg/L, respectively. The method was applied to determine perchlorate and bromate concentrations in total of 23 selected Missouri drinking water treatment systems during differing seasons. The water systems selected include different source waters: groundwater, lake water, river water, and groundwater influenced by surface water. The concentrations of perchlorate and bromate were lower than or near to method detection limits in most of the drinking water samples monitored. The removal of perchlorate by various adsorbents was studied. A cationic organoclay (TC-99) exhibited effective removal of perchlorate from drinking water matrices.

  7. The Effect of Anionic, Cationic and Nonionic Surfactants on the Uncatalyzed Bromate Oscillator

    Science.gov (United States)

    Grančičová, Ol'ga; Olexová, Anna; Zacher, Tomáš

    2008-08-01

    The response of an uncatalyzed bromate oscillator with phenol as substrate to the increasing concentrations of cationic (CTAN), anionic (SDS) and nonionic surfactants (Brij-30 and Triton X-100) was monitored at (25±0.1) °C under stirred batch conditions. Addition of the surfactants influenced the oscillatory parameters: a slight increase of the induction period of the first series of oscillations, a significant increase of the induction period of the second series of oscillations and a gradual decrease of the oscillation numbers of both series until complete disappearance at a certain surfactant concentration. The changes in the oscillatory parameters have been ascribed to solubilization of phenol and of bromination products in the micelles, to inhibition of bromination of the aromatic substrate due to bromine solubilization, and to the catalytic effect of the charged micelle surface.

  8. Chemiluminescence determination of potassium bromate in flour based on flow injection analysis.

    Science.gov (United States)

    Yan, Zhengyu; Zhang, Zhengwei; Yu, Yan; Liu, Zhen; Chen, Jianqiu

    2016-01-01

    A novel and highly sensitive flow-injection chemiluminescence method for the determination of potassium bromate (KBrO3) has been developed. This method is based on the luminescence properties of the KBrO3-Na2SO3-quinine sulfate system in acid medium. Optimized experimental conditions and a possible mechanism were investigated. The relative chemiluminescence intensity responded linearly to the concentration of KBrO3 in the range of 7.054 × 10(-6)-1.008 × 10(-4) mol/L with a detection limit of 2.116 × 10(-6) mol/L. The relative standard deviation (RSD) at 5.0 × 10(-5) mol/L KBrO3 (n = 12) was 2.3%. The proposed method was applied successfully to the determination of KBrO3 in flour. Copyright © 2015 Elsevier Ltd. All rights reserved.

  9. Determination of trace amount of formaldehyde base on a bromate-Malachite Green system

    Science.gov (United States)

    Tang, Yufang; Chen, Hao; Weng, Chao; Tang, Xiaohui; Zhang, Miaoling; Hu, Tao

    2015-01-01

    A novel catalytic kinetic spectrophotometric method for determination of trace amount of formaldehyde (FA) has been established, based on catalytic effect of trace amount of FA on the oxidation of Malachite Green (MG) by potassium bromate in presence of sulfuric acid medium, and was reported for the first time. The method was monitored by measuring the decrease in absorbance of MG at 617 nm and allowed a precise determination of FA in the range of 0.003-0.08 μg mL-1, with a limit of detection down to 1 ng mL-1. The relative standard deviation of 10 replicate measurements was 1.63%. The method developed was approved to be sensitive, selective and accurate, and adopted to determinate free FA in samples directly with good accuracy and reproducibility.

  10. Direct injection, simple and robust analysis of trace-level bromate and bromide in drinking water by IC with suppressed conductivity detection.

    Science.gov (United States)

    Lawal, Wasiu; Gandhi, Jay; Zhang, Chunlong Carl

    2010-08-01

    Bromide is ubiquitously found in drinking water. It is introduced into source water primarily by contact with bromide-containing soils or seawater having high bromide content. Bromide is converted into carcinogenic bromate during ozonation processes employed in some drinking water and wastewater treatment plants. Therefore, monitoring of bromate in drinking water and its precursor bromide in source water is required. The purpose of this study was to survey bromide and bromate concentrations in randomly selected bottle waters of various brands and several tap water samples in the coastal Houston area using a direct-injection ion chromatography (IC) and a suppressed conductivity system. The method employs a simple isocratic IC with loop injection with calculated detection limit of 0.009 microg/L for bromate and 0.028 microg/L for bromide (250-microL sample volume). Allowing the detection of both species at the microg/L level in drinking water, this method does not require specialized instrumentation such as two-dimensional IC, expensive sample preparation, or post-column reactions. The results show that, whereas bromate remains undetected in all five tap water samples, there are significant high concentrations of bromide in the coastal Houston area (294.79 +/- 56.97 microg/L). Its link to potential seawater intrusion need to be further investigated. For bottle water samples randomly collected, 18.2% (2 out of 11) showed detectable amount of both bromide and bromate. The detection of bromate coincides with those bottle water samples that underwent ozonation treatment. Further sample campaign with exclusively ozonated bottle water samples (n = 19) showed 100% detection rate for both bromide and bromate. The 99% confidence intervals were 14.45-37.97 microg/L and 0.32-2.58 microg/L for bromide and bromate, respectively. The highest level of bromate among all ozonated bottle water samples was 7.57 microg/L, a concentration close to the U.S. EPA prescribed limit for

  11. Anti-Nutritional Factors and Potassium Bromate Content in Bread and Flour Samples in Uyo Metropolis, Nigeria

    Directory of Open Access Journals (Sweden)

    A. S. Ekop

    2008-01-01

    Full Text Available The aim of the study is to evaluate the anti-nutritional composition factors and potassium bromate content of some selected bread and flour samples in Uyo Metropolis. The result of the analysis shows that, though the concentration of phytic acid and tannins was high in both the bread and flour samples their concentrations did not exceed lethal doses. The potassium bromate content was minimal in all the bread and flour samples and within safe limits of residual bromide found in flour as specified by the US Food and Drug Administration. The concentrations of the anti-nutritional factors in the bread and flour samples were partially different from each other when subjected to the students t-test statistics.

  12. Termination of nanoscale zero-valent iron reactivity by addition of bromate as a reducing reactivity competitor

    Science.gov (United States)

    Mines, Paul D.; Kaarsholm, Kamilla M. S.; Droumpali, Ariadni; Andersen, Henrik R.; Lee, Wontae; Hwang, Yuhoon

    2017-09-01

    Remediation of contaminated groundwater by nanoscale zero-valent iron (nZVI) is widely becoming a leading environmentally friendly solution throughout the globe. Since a wide range of various nZVI-containing materials have been developed for effective remediation, it is necessary to determine an appropriate way to terminate the reactivity of any nZVI-containing material for a practical experimental procedure. In this study, bimetallic Ni/Fe-NPs were prepared to enhance overall reduction kinetics owing to the catalytic reactivity of nickel on the surface of nZVI. We have tested several chemical strategies in order to terminate nZVI reactivity without altering the concentration of volatile compounds in the solution. The strategies include surface passivation in alkaline conditions by addition of carbonate, and consumption of nZVI by a reaction competitor. Four halogenated chemicals, trichloroethylene, 1,1,1-trichloroethane, atrazine, and 4-chlorophenol, were selected and tested as model groundwater contaminants. Addition of carbonate to passivate the nZVI surface was not effective for trichloroethylene. Nitrate and then bromate were applied to competitively consume nZVI by their faster reduction kinetics. Bromate proved to be more effective than nitrate, subsequently terminating nZVI reactivity for all four of the tested halogenated compounds. Furthermore, the suggested termination method using bromate was successfully applied to obtain trichloroethylene reduction kinetics. Herein, we report the simple and effective method to terminate the reactivity of nZVI by addition of a reducing reactivity competitor.

  13. Association of brominated proteins and changes in protein expression in the rat kidney with subcarcinogenic to carcinogenic doses of bromate

    Energy Technology Data Exchange (ETDEWEB)

    Kolisetty, Narendrababu [Department of Pharmaceutical and Biomedical Sciences, College of Pharmacy, University of Georgia, Athens, GA 30602 (United States); Bull, Richard J. [MoBull Consulting, Richland, WA 99352 (United States); Muralidhara, Srinivasa; Costyn, Leah J. [Department of Pharmaceutical and Biomedical Sciences, College of Pharmacy, University of Georgia, Athens, GA 30602 (United States); Delker, Don A. [School of Medicine, University of Utah, Salt Lake City, UT 84132 (United States); Guo, Zhongxian [Water Quality Office, Public Utilities Board, 608576 (Singapore); Cotruvo, Joseph A. [Joseph Cotruvo and Associates, LLC, Washington, DC 20016 (United States); Fisher, Jeffrey W. [National Center for Toxicological Research, FDA, Jefferson, AR 72079 (United States); Cummings, Brian S., E-mail: bsc@rx.uga.edu [Department of Pharmaceutical and Biomedical Sciences, College of Pharmacy, University of Georgia, Athens, GA 30602 (United States)

    2013-10-15

    The water disinfection byproduct bromate (BrO{sub 3}{sup −}) produces cytotoxic and carcinogenic effects in rat kidneys. Our previous studies demonstrated that BrO{sub 3}{sup −} caused sex-dependent differences in renal gene and protein expression in rats and the elimination of brominated organic carbon in their urine. The present study examined changes in renal cell apoptosis and protein expression in male and female F344 rats treated with BrO{sub 3}{sup −} and associated these changes with accumulation of 3-bromotyrosine (3-BT)-modified proteins. Rats were treated with 0, 11.5, 46 and 308 mg/L BrO{sub 3}{sup −} in drinking water for 28 days and renal sections were prepared and examined for apoptosis (TUNEL-staining), 8-oxo-deoxyguanosine (8-oxoG), 3-BT, osteopontin, Kim-1, clusterin, and p-21 expression. TUNEL-staining in renal proximal tubules increased in a dose-related manner beginning at 11.5 mg BrO{sub 3}{sup −}/L in female rats and 46 mg/L in males. Increased 8-oxoG staining was observed at doses as low as 46 mg/L. Osteopontin expression also increased in a dose-related manner after treatment with 46 mg/L, in males only. In contrast, Kim-1 expression increased in a dose-related manner in both sexes, although to a greater extent in females at the highest dose. Clusterin and p21 expression also increased in a dose-related manner in both sexes. The expression of 3-BT-modified proteins only increased in male rats, following a pattern previously reported for accumulation of α-2{sub u}-globulin. Increases in apoptosis in renal proximal tubules of male and female rats at the lowest doses suggest a common mode of action for renal carcinogenesis for the two sexes that is independent of α-2{sub u}-globulin nephropathy. - Highlights: • Bromate induced nephrotoxicity in both male and female rats by similar mechanisms. • Apoptosis was seen in both male and female rats at the lowest doses tested. • Bromate-induced apoptosis correlated to 8-oxo

  14. Bromate formation from the oxidation of bromide in the UV/chlorine process with low pressure and medium pressure UV lamps.

    Science.gov (United States)

    Fang, Jingyun; Zhao, Quan; Fan, Chihhao; Shang, Chii; Fu, Yun; Zhang, Xiangru

    2017-09-01

    When a bromide-containing water is treated by the ultraviolet (UV)/chlorine process, hydroxyl radicals (HO) and halogen radicals such as Cl or Br are formed due to the UV photolysis of free halogens. These reactive species may induce the formation of bromate, which is a probable human carcinogen. Bromate formation in the UV/chlorine process using low pressure (LP) and medium pressure (MP) lamps in the presence of bromide was investigated in the present study. The UV/chlorine process significantly enhanced bromate formation as compared to dark chlorination. The bromate formation was elevated with increasing UV fluence, bromide concentration, and pH values under both LP and MP UV irradiations. It was significantly enhanced at pH 9 compared to those at pH 6 and 7 with MP UV irradiation, while it was slightly enhanced at pH 9 with LP UV. The formation by UV/chlorine process started with the formation of free bromine (HOBr/OBr-) through the reaction of chlorine and bromide, followed by a subsequent oxidation of free bromine and formation of BrO and bromate by reacting with radicals. Copyright © 2017 Elsevier Ltd. All rights reserved.

  15. [Determination of trace and ultra-trace level bromate in water by large volume sample injection with enrichment column for on-line preconcentration coupled with ion chromatography].

    Science.gov (United States)

    Liu, Jing; He, Qingqing; Yang, Lili; Hu, Enyu; Wang, Meifei

    2015-10-01

    A method for the determination of trace and ultra-trace level bromate in water by ion chromatography with large volume sample injection for on-line preconcentration was established. A high capacity Dionex IonPac AG23 guard column was simply used as the enrichment column instead of the loop for the preconcentration of bromate. High purity KOH solution used as eluent for gradient elution was on-line produced by an eluent generator automatically. The results showed that a good linear relationship of bromate was exhibited in the range of 0.05-51.2 μg/L (r ≥ 0.999 5), and the method detection limit was 0.01 μg/L. Compared with conventional sample injection, the injection volume was up to 5 mL, and the enrichment factor of this method was about 240 times. This method was successfully applied for several real samples of pure water which were purchased in the supermarket, and the recoveries of bromate were between 90%-100% with the RSDs (n = 6) of 2.1%-6.4% at two spiked levels. This method without pretreatment is simple, and of high accuracy and precision. The preconcentration can be achieved by large volume sample injection. It is suitable for the analysis of trace and ultra-trace level bromate.

  16. Sensitive and simple determination of bromate in foods disinfected with hypochlorite reagents using high performance liquid chromatography with post-column derivatization.

    Science.gov (United States)

    Yokota, Azusa; Kubota, Hiroki; Komiya, Satomi; Sato, Kyoko; Akiyama, Hiroshi; Koshiishi, Ichiro

    2012-11-02

    A novel analytical method for the quantification of bromate in fresh foods using high performance liquid chromatography (HPLC) with a post-column reaction has been developed. The fresh food sample solutions were pretreated with homogenization, centrifugal ultrafiltration and subsequent solid phase extraction using a strong anion-exchange resin. After separation on a strong anion-exchange chromatography column using a highly concentrated NaCl solution (0.3M) as the eluent, the bromate was quantified by detection using a post-column reaction with a non-carcinogenic reagent (tetramethylbenzidine). The developed HPLC technique made it possible to quantify bromate in salt-rich fresh foods. The recoveries from fresh foods spiked with bromate at low levels (2 or 10 ng/g) satisfactorily ranged from 75.3 to 90.7%. The lowest quantification limit in fresh foods was estimated to be 0.6 ng/g as bromic acid. The method should be helpful for the quantification of bromate in fresh foods disinfected with hypochlorite solutions. Copyright © 2012 Elsevier B.V. All rights reserved.

  17. Bromate inhibition by reduced graphene oxide in thermal/PMS process.

    Science.gov (United States)

    Huang, Xin; Zhou, Xujie; Zhou, Jizhi; Huang, Zhifeng; Liu, Shuang; Qian, Guangren; Gao, Naiyun

    2017-10-01

    Bromate (BrO3(-)), as a contaminant producing from bromide (Br(-)) oxidation, has been revealed for generation in sulfate radical involved processes. In this work, reduced graphene oxide (rGO) was firstly applied to inhibit the formation of BrO3(-) in thermally activated peroxymonosulfate (thermal/PMS) treatment. In the presence of 5-35 mg/L rGO, the decomposition rate of PMS was slightly increased from 0.0162 ± 0.0013 min(-1) to 0.0200 ± 0.0010 min(-1), corresponding to removal rate of target pollutant increasing from 0.0157 ± 0.0012 min(-1) to 0.0204 ± 0.0022 min(-1). This suggested the decay of PMS, the concentration and distribution of radicals were not influenced dramatically by the addition of rGO, which was partly supported by the almost unchanged HPLC chromatograms as compared with that in the absence of rGO. However, the produced BrO3(-) was significantly lowered by 67%-100% with the addition of rGO in a wide range of pH at 5-9 and activation temperature at 60-80 °C. Moreover, a quick reduction of hypobromous acid (HOBr) to Br(-) was achieved with addition of rGO at room temperature, whilst no abatement of BrO3(-) and Br(-) was observed in the same conditions. Therefore, masking HOBr was probably the role of rGO on bromate inhibition in thermal/PMS process. Because HOBr is a requisite intermediate for BrO3(-), the inhibition effect of rGO is likely irrelevant of oxidation processes, which was inevitably showed by the good performance of rGO on BrO3(-) suppress in ozonation. Therefore, the addition of rGO in tens of mg/L is a promising measure to avoid the formation of unwanted bromine species in advanced oxidation processes. Copyright © 2017. Published by Elsevier Ltd.

  18. Flow-injection spectrophotometric determination of bromate in bottled drinking water samples using chlorpromazine reagent and a liquid waveguide capillary cell.

    Science.gov (United States)

    Tóth, Ildikó V; Santos, Inês C; Azevedo, Cláudia F M; Fernandes, Jorge F S; Páscoa, Ricardo N M J; Mesquita, Raquel B R; Rangel, António O S S

    2013-01-01

    In this work, aiming to develop a simple, inexpensive method for the determination of low bromate levels in water samples, a liquid waveguide capillary cell (LWCC) was coupled to a FIA system. The long optical path (100 cm) of the LWCC was used to improve the sensitivity and the limit of detection without resorting to any off-line or in-line preconcentration processes. The spectrophotometric determination was based on the oxidation of chlorpromazine by bromate in an acidic medium, resulting in the formation of a colored radical product. Sulfamic acid was added to the reagent for minimizing the interference of nitrite, and a chelating ion exchange resin was used to remove major cationic interferences. The developed system allowed the determination of bromate within the range between 1 - 20 μg L(-1) with a detection limit of 0.2 μg L(-1).

  19. Extractive liquid-liquid spectrofluorometric determination of trace and ultra concentrations of bromate in water samples by the fluorescence quenching of tetraphenylphosphonium iodide

    Science.gov (United States)

    Al-Saidi, H. M.; El-Shahawi, M. S.

    2015-03-01

    A low cost and selective spectrofluorimetric method has been developed for trace determination of bromate ions in water. The method has been based upon complete extraction of the produced yellow colored ion associate of the reagent tetraphenylphosphonium iodide (TPP+ I-) and bromate ions from aqueous media into chloroform and measuring the fluorescence quenching at λex/em = 242/305 nm. The composition, stability and the most probable mechanism of the produced associate have been determined. The plot of fluorescence intensity of TPP+ I-vs. bromate concentration was linear in the range 0.86-150.0 μg L-1. The limits of detection (LOD) and quantification (LOQ) of BrO3- were 0.24 and 0.76 μg L-1, respectively. The method was found free from most of the interferences present in chromatographic, spectrofluorometric and spectrophotometric methods. Intra and inter-day laboratory accuracy and precision for analysis of bromate in water were determined. The method provides better performance compared to the international standard method recently issued (ISO 11206:2011). The method was applied satisfactorily for analysis of 1.0 μg L-1 bromate in the presence of high excess of chloride (50 mg/L) without pretreatment with a relative standard deviation (RSD) of ±2.9%. The method was applied for analysis of bromate in various water samples. Statistical comparison of the results of the proposed method with those obtained by the standard method revealed no significant differences in the accuracy and precision.

  20. Rapid analysis of perchlorate, chlorate and bromate ions in concentrated sodium hypochlorite solutions.

    Science.gov (United States)

    Pisarenko, Aleksey N; Stanford, Benjamin D; Quiñones, Oscar; Pacey, Gilbert E; Gordon, Gilbert; Snyder, Shane A

    2010-02-05

    A sensitive, rapid, and rugged liquid chromatography with tandem mass spectrometry (LC-MS/MS) method for measuring concentrations of perchlorate, chlorate, and bromate ions in concentrated sodium hypochlorite solutions is presented. The LC-MS/MS method offers a practical quantitation limit (PQL) of 0.05 microg L(-1) for ClO(4)(-), 0.2 microg L(-1) for BrO(3)(-), and 0.7 microg L(-1) for ClO(3)(-) and a sample analysis time of only 10 min. Additionally, an iodometric titration technique was compared with the LC-MS/MS method for measurement of chlorate ion at high concentration. The LC-MS/MS method was the most reproducible for chlorate concentrations below 0.025 M while the iodometric titration method employed was the most reproducible above 0.025 M. By using both methods, concentrations of chlorate can be measured over a wide range, from 0.7 microg L(-1) to 210 g L(-1) in hypochlorite ion solutions. Seven quenching agents were also evaluated for their ability to neutralize hypochlorite ion, thereby stopping formation of perchlorate ion in solution, without adversely impacting the other oxyhalide ions. Malonic acid was chosen as the quenching agent of choice, meeting all evaluation criteria outlined in this manuscript. Copyright 2009 Elsevier B.V. All rights reserved.

  1. Treatment of Aqueous Bromate by Superparamagnetic BiOCl-Mediated Advanced Reduction Process

    Directory of Open Access Journals (Sweden)

    Xiaowei Liu

    2017-05-01

    Full Text Available Bromate ( BrO 3 − contamination in drinking water is a growing concern. Advanced reduction processes (ARPs are reportedly promising in relieving this concern. In this work, UV/superparamagnetic BiOCl (BiOCl loaded onto superparamagnetic hydroxyapatite assisted with small molecule carboxylic acid (formate, citrate, and acetate, a carboxyl anion radical ( CO 2 • − -based ARP, was proposed to eliminate aqueous BrO 3 − . Formate and citrate were found to be ideal CO 2 • − precursor, and the latter was found to be safe for practical use. BrO 3 − (10 μg·L−1, WHO guideline for drinking water can be completely degraded within 3 min under oxygen-free conditions. In this process, BrO 3 − degradation was realized by the reduction of CO 2 • − (major role and formyloxyl radical (minor role in bulk solution. The formation mechanism of radicals and the transformation pathway of BrO 3 − were proposed based on data on electron paramagnetic resonance monitoring, competitive kinetics, and degradation product analysis. The process provided a sustainable decontamination performance (<5% deterioration for 10 cycles and appeared to be more resistant to common electron acceptors (O2, NO 3 − , and Fe3+ than hydrated electron based-ARPs. Phosphate based-superparamagnetic hydroxyapatite, used to support BiOCl in this work, was believed to be applicable for resolving the recycling problem of other metal-containing catalyst.

  2. Photocatalytic decomposition of bromate ion by the UV/P25-Graphene processes.

    Science.gov (United States)

    Huang, Xin; Wang, Longyong; Zhou, Jizhi; Gao, Naiyun

    2014-06-15

    The photocatalysis of bromate (BrO3(-)) attracts much attention as BrO3(-) is a carcinogenic and genotoxic contaminant in drinking water. In this work, TiO2-graphene composite (P25-GR) photocatalyst for BrO3(-) reduction were prepared by a facile one-step hydrothermal method, which exhibited a higher capacity of BrO3(-) removal than P25 or GR did. The maximum removal of BrO3(-) was observed in the optimal conductions of 1% GR doping and at pH 6.8. Compared with that without UV, the higher decreasing of BrO3(-) on the composite indicates that BrO3(-) decomposition was predominantly contributed to photo-reduction with UV rather than adsorption. This hypothesis was supported by the decreasing of [BrO3(-)] with the synchronous increasing of [Br(-)] at nearly constant amount of total Bromine ([BrO3(-)] + [Br(-)]). Furthermore, the improvement of BrO3(-) reduction on P25-GR was observed in the treatment of a tap water. However, the efficiency of BrO3(-) removal was less than that in deionized water, probably due to the consumption of photo-generated electrons and the adsorption of natural organic matters (NOM) on graphene. Copyright © 2014. Published by Elsevier Ltd.

  3. Research on Efficiency of Ozonation and Bromate Formation in Low Temperature and Low Turbidity Water

    Science.gov (United States)

    Zhu, Qi; Liu, Dongmei; Cui, Fuyi; Fang, Lei; Zhao, Zhiwei; Liu, Tongmian

    2010-11-01

    The efficiency of ozonation and the influence factor of bromate formation were studied in filtered water at low temperature and low turbidity in Harbin Shaohe water treatment plant, of which source water was from Songhua river. The results showed that when adding 3 mg/L O3 to the filtered water, the average removal rate of UV254 were 22.31%, the removal rate of TOC in filtered water were 6.33%. When adding 2 mg/L O3 and 4 mg/L O3 to the filtered water, the CODMn decreased by 21.53% and 24.68%, respectively. Ozonation had no obvious effect on reducing turbidity and the content of ammonia nitrogen of filtered water in Shaohe water treatment plant. It could be found that the formation amount of BrO3- would increase with the concentration of Br- increasing in low temperature and low turbidity water. When Ct value of filtered water in Shaohe water treatment plant was less than 30 mgṡL-1ṡmin, the formation amount of BrO3- could be controlled under 10 μg/L.

  4. Formation of brominated disinfection by-products and bromate in cobalt catalyzed peroxymonosulfate oxidation of phenol.

    Science.gov (United States)

    Liu, Kuo; Lu, Junhe; Ji, Yuefei

    2015-11-01

    Formation of halogenated disinfection by-products (DBPs) in sulfate radical [Formula: see text] based oxidation processes attracted considerable attention recently. However, the underlying reaction pathways have not been well explored. This study focused on the transformation of Br(-) in cobalt activated peroxymonosulfate (Co(2+)/PMS) oxidation process. Phenol was added as a model compound to mimic the reactivity of natural organic matter (NOM). It was revealed that Br(-) was efficiently transformed to reactive bromine species (RBS) including free bromine and bromine radicals (Br, [Formula: see text] , etc.) in Co(2+)/PMS system. [Formula: see text] played a principal role during this process. RBS thus generated resulted in the bromination of phenol and formation brominated DBPs (Br-DBPs) including bromoform and bromoacetic acids, during which brominated phenols were detected as the intermediates. Br-DBPs were further degraded by excessive [Formula: see text] and transformed to bromate ultimately. Free bromine was also formed in the absence of Co(2+), suggesting Br(-) could be oxidized by PMS per se. Free bromine was incorporated to phenol sequentially leading to Br-DBPs as well. However, Br-DBPs could not be further transformed in the absence of [Formula: see text] . This is the first study that elucidated the comprehensive transformation map of Br(-) in PMS oxidation systems, which should be taken into consideration when PMS was applied to eliminate contamination in real practice. Copyright © 2015 Elsevier Ltd. All rights reserved.

  5. Ameliorative effects of vanillin on potassium bromate induces bone and blood disorders in vivo.

    Science.gov (United States)

    Ben Saad, H; Ben Amara, I; Krayem, N; Boudawara, T; Kallel, C; Zeghal, K M; Hakim, A

    2015-11-08

    The objective of this study was to investigate the propensity of potassium bromate (KBrO3) to induce oxidative stress in blood and bone of adult mice and its possible attenuation by vanillin. Our results demonstrated, after KBrO3 treatment, a decrease of red blood cells and hemoglobin and a significant increase of white blood cell. A decrease in plasma levels of folic acid, vitamin B12 and iron was also noted. Interestingly, an increase of lipid peroxidation, hydroperoxides, hydrogen peroxide, advanced oxidation protein products and protein carbonyl levels in erythrocytes and bone was observed, while superoxide dismutase, catalase and glutathione peroxidase activities and glutathione, non-protein thiol and vitamin C levels were decreased. KBrO3 treatment resulted in blood and bone DNA fragmentation, a hallmark of genotoxicity-KBrO3-induced, with reduction of DNA levels. Calcium and phosphorus levels showed a decrease in the bone and an increase in the plasma after KBrO3 treatment. These biochemical alterations were accompanied by histological changes in the blood smear and bone tissue. Treatment with vanillin improved the histopathological, hematotoxic and genotoxic effects induced by KBrO3. The results showed, for the first time, that the vanillin possesses a potent protective effect against the oxidative stress and genotoxicity in bone and blood of KBrO3-treated mice.

  6. Oxidative treatment of fentanyl compounds in water by sodium bromate combined with sodium sulphite.

    Science.gov (United States)

    Xu, Lin; Ren, Lijun; Wang, Zhihua; Tian, Xingtao; Qi, Lihong; Fan, Qiping; Xiang, Yulian

    2015-01-01

    As narcotic analgesics, fentanyl compounds have been commonly produced and widely used during surgical procedures. The residual and waste of fentanyl compounds have potential harmful impacts on the environment and human health. The oxidative degradation of fentanyl compounds by sodium bromate mixed systems was studied. Factors influencing the oxidation reaction, including molar ratio of NaBrO3/H(+)/SO3(2-), molar ratio of NaBrO3/fentanyl and pH, were investigated. Fentanyl, carfentanil and 3-methylfentanyl were able to be completely degraded in 30 minutes by a NaBrO3 mixed system under optimum conditions, the molar ratio of NaBrO3/H(+)/SO3(2-) equal to 20:3:10, the molar ratio of NaBrO3:fentanyl compounds 50:1 and pH = 4. Sufentanil was only able to be degraded by 74% under the same conditions. The degradation products of the fentanyl compounds detected and identified by gas chromatography/mass spectrometry suggested several possible degradation pathways.

  7. Bromate Removal from Water Using Doped Iron Nanoparticles on Multiwalled Carbon Nanotubes (CNTS

    Directory of Open Access Journals (Sweden)

    Aasem Zeino

    2014-01-01

    Full Text Available The raw carbon nanotubes (CNTs were prepared by the floating catalyst chemical vapor deposition method. The raw carbon nanotubes were functionalized, impregnated with iron nanoparticles, and characterized using high resolution transmission electron microscopy (HRTEM, scanning electron microscopy with energy dispersive spectroscopy (SEM-EDS, Fourier transform infrared spectroscopy (FTIR, Differential Scanning Calorimetry (DSC, and thermogravimetric analysis (TGA. The three types of these multiwalled carbon nanotubes were applied as adsorbents for the removal of bromate from drinking water. The effects of the pH, the concentration of BrO3- anion, the adsorbent dose, the contact time, and the coanions on the adsorption process have been investigated. The results concluded that the highest adsorption capacities were 0.3460 and 0.3220 mg/g through using CNTs-Fe and raw CNTs, respectively, at the same conditions. The results showed that the CNTs-Fe gives higher adsorption capacity compared with the raw CNTs and the functionalized CNTs. The presence of nitrate (NO3- in the solution decreases the adsorption capacity of all CNTs compared with chloride (Cl- associated with pH adjustment caused by nitric acid or hydrochloric acid, respectively. However, the adsorption of all MWNCTs types increases as the pH of solution decreases.

  8. Determination of ranitidine hydrochloride in pharmaceutical preparations by titrimetry and visible spectrophotometry using bromate and acid dyes.

    Science.gov (United States)

    Basavaiah, K; Nagegowda, P

    2004-02-01

    Four new methods using titrimetry and spectrophotometry are described for the determination of ranitidine hydrochloride (RNH) with potassium bromate as the oxidimetric reagent and acid dyes, methyl orange, indigo carmine and metanil yellow. In direct titrimetry (method A), the drug is titrated directly with bromate in acid medium and in the presence of excess of bromide using methyl orange indicator. In back titrimetry (method B), the drug is treated with a measured excess of bromate in the presence of bromide and acid, and the unreacted bromine is determined iodometrically. Both spectrophotometric methods are based on the oxidation of RNH by a known excess of bromate in acid medium and in the presence of excess of bromide followed by estimation of surplus oxidant by reacting with either indigo carmine (method C) or metanil yellow (method D), and measuring the absorbance at 610 or 530 nm. In methods B, C and D, reacted oxidant corresponds to the drug content. The experimental conditions are optimized. Titrimetric procedures are applicable over the ranges 1-10 mg (A) and 1-17 mg (B), and the reaction stoichiometry is found to be 1:1 (BrO(-)(3): RNH). In spectrophotometric methods, the absorbance is found to increase linearly with increasing concentration of RNH, which is corroborated by the calculated correlation coefficient (r) of 0.9984 (C) and 0.9976 (D). The systems obey Beer's law for 2-12 and 1-7 microg ml(-1), for methods C and D, respectively. Method D with a molar absorptivity of 9.82 x 10(4) l mol(-l) cm(-1) is found to be more sensitive than method C ( epsilon = 2.06 x l0(4) l mol(-1) cm(-1)). The limits of detection and quantification are reported for both the spectrophotometric methods. The proposed methods were applied successfully to the determination of RNH in tablets and injections. The reliability of the assay was established by parallel determination by the official method and by recovery studies.

  9. [Mg/Al layered double hydroxides prepared by microwave-assisted co-precipitation method for the removal of bromate].

    Science.gov (United States)

    Zhong, Qiong; Li, Huan

    2014-04-01

    In this paper, Mg/Al layered double hydroxides (Mg/Al LDHs) were prepared by the microwave-assisted co-precipitation method and the conventional co-precipitation method. The samples were labeled as Mg/Al LDHs-MW and Mg/Al LDHs-H, respectively. Mg/Al LDHs were characterized by X-ray diffractometer (XRD), Brunauer-Emmett-Teller (BET), scanning electron microscopy (SEM) and Fourier transform infrared (FT-IR). The results showed that the application of microwave in the preparation process promoted the formation of smaller pore diameter and higher crystallinity particles. The pore size and particle size of Mg/Al LDHs-MW were 41.13 nm and 427.08 nm, respectively. Batch experiments were investigated to evaluate the effect of dosage, initial pH and regeneration frequencies for bromate removal. The conclusion showed that the process of bromate removal on Mg/Al LDHs could be described by the pseudo-second kinetic model. The Langmuir isotherm well described the experimental data, and the Mg/Al LDHs-MW has a stronger adsorption capacity while the maximum adsorption capacity (q(0)) of Mg/Al LDHs-MW for bromate was 321.26 microg x g(-1) which was larger than the q(0) (288.74 microg x g(-1)) of Mg/Al LDHs-H. For the continuous fixed-bed column, model simulations using the Thomas model showed that the experimental data obtained at three different columns packed with Mg/Al LDHs-MW were able to predict breakthrough curves. Simulating the maximum adsorption capacity of adsorption column for bromate removal was 288.81 microg x g(-1). When the bed depth was 10 cm, inlet concentration was 800 microg x L(-1) and flow rate was 4.0 mL x min, the correlation coefficient of model was 0.92, indicating that the experimental data was described well by the Thomas model.

  10. Front propagation in the bromate-sulfite-ferrocyanide-aluminum (III) system: Autocatalytic front in a buffer system

    Science.gov (United States)

    Kovacs, Klara; Leda, Marcin; Vanag, Vladimir K.; Epstein, Irving R.

    2010-06-01

    We study the propagation of pH fronts in a narrow, pseudo-one-dimensional strip of gel containing bromate, sulfite, ferrocyanide and aluminum ions. The front propagation speed v decreases with [ Al 3+] as 1/v=1/v0+c[Al], where c is a constant. We determine the diffusion coefficients of protons and ferricyanide ions and find that Al(OH) 3 loaded in agarose or acrylamide gels binds protons reversibly, thereby slowing the propagating fronts without significantly affecting the diffusion of ferricyanide ions. We present a model that qualitatively reproduces the experimental behavior, and we suggest some general principles governing autocatalytic fronts in buffered systems.

  11. Oxyhalogen-sulfur chemistry: kinetics and mechanism of oxidation of captopril by acidified bromate and aqueous bromine.

    Science.gov (United States)

    Kapungu, G P; Rukweza, G; Tran, Thai; Mbiya, Wilbes; Adigun, Risikat; Ndungu, Patrick; Martincigh, Bice; Simoyi, Reuben H

    2013-04-04

    By nature of their nucleophilicity, all thiol-based drugs are oxidatively metabolized in the physiological environment. The key to understanding the physiological role of a hypertension drug, (2S)-1-[(2S)-2-methyl-3-sulfanylpropanoyl]pyrrolidine-2-carboxylic acid, medically known as captopril is through studying its oxidation pathway: its reactive intermediates and oxidation products. The oxidation of captopril by aqueous bromine and acidified bromate has been studied by spectrophotometric and electrospray ionization techniques. The stoichiometry for the reaction of acidic bromate with captopril is 1:1, BrO3(-) + (C4H6N)(COOH)(COCHCH3CH2)-SH → (C4H6N)(COOH)(COCHCH3CH2)-SO3H + Br(-), with reaction occurring only at the thiol center. For the direct reaction of bromine with captopril, the ratio is 3:1; 3Br2 + (C4H6N)(COOH)(COCHCH3CH2)-SH + 3H2O → (C4H6N)(COOH)(COCHCH3CH2)-SO3H + 6HBr. In excess acidic bromate conditions the reaction displays an initial induction period followed by a sharp rise in absorbance at 390 nm due to rapid formation of bromine. The direct reaction of aqueous bromine with captopril was much faster than oxidation of the thiol by acidified bromate, with a bimolecular rate constant of (1.046 (±0.08) × 10(5) M(-1) s(-1). The detection of thiyl radicals confirms the involvement of radicals as intermediates in the oxidation of Captopril by acidified BrO3(-). The involvement of thiyl radicals in oxidation of captopril competes with a nonradical pathway involving 2-electron oxidations of the sulfur center. The oxidation product of captopril under these strong oxidizing conditions is a sulfonic acid as confirmed by electrospray ionization mass spectrometry (ESI-MS), iodometric titrations, and proton nuclear magnetic resonance ((1)H NMR) results. There was no evidence from ESI-MS for the formation of the sulfenic and sulfinic acids in the oxidation pathway as the thiol group is rapidly oxidized to the sulfonic acid. A computer simulation analysis of

  12. OXIDATIVE DNA DAMAGE FROM POTASSIUM BROMATE EXPOSURE IN LONG-EVANS RATS IS NOT ENHANCED BY A MIXTURE OF DRINKING WATER DISINFECTION BY-PRODUCTS

    Science.gov (United States)

    Public drinking water treated with chemical disinfectants contains a complex mixture of disinfection by-products (DBPs) for which the relative toxicity of the mixtures needs to be characterized to accurately assess risk. Potassium bromate (KBrO3) is a by-product from ozonation of...

  13. Creation of Pd/Al2O3 Catalyst by a Spray Process for Fixed Bed Reactors and Its Effective Removal of Aqueous Bromate

    Science.gov (United States)

    Gao, Yu; Sun, Wuzhu; Yang, Weiyi; Li, Qi

    2017-02-01

    Palladium nanoparticles were grown on sub-millimeter activated Al2O3 particle support by spraying H2PdCl4 solution evenly onto the support, followed with a thermal reduction under H2 atmosphere. Compared with its counterpart created by the conventional impregnation method, the Pd/Al2O3 catalyst created by the spray process could enrich the existence of active Pd nanoparticles on the surface of the catalyst support and increase their degree of dispersion, resulting in a much higher activity in the catalytic reduction of bromate in water. The effect of Al2O3 support particle size on the bromate removal rate was also investigated, which demonstrated that smaller support particle size could have higher activity in the catalytic reduction of bromate in water because of its larger exposed surface. This Pd/Al2O3 catalyst could be easily used in the fixed bed reactor due to its large support size and demonstrated excellent stability in the catalytic reduction of bromate in mineral water. This Pd/Al2O3 catalyst also exhibited a good catalytic reduction performance on azo dyes as demonstrated by its effective catalytic hydrogenation of methyl orange. Thus, catalysts prepared by the spray method developed in this work could have the potential to be used in fixed bed reactors for various water treatment practices.

  14. Photocatalytic Reduction Activity of 001  TiO2 Codoped with F and Fe under Visible Light for Bromate Removal

    Directory of Open Access Journals (Sweden)

    Yan Zhang

    2016-01-01

    Full Text Available The presence of bromate in water is a well-known problem because of its toxic effects on human health, particularly its carcinogenic potential. Photocatalytic reduction is an attractive process for bromate removal. F- and Fe-codoped TiO2 (F-Fe-TiO2 with a {001} facet was successfully prepared, and its bromate-removal activity under visible light was examined. The microstructure, morphology, and chemical state of the doping elements and the optical property of the photocatalysts were examined using transmission electron microscopy (TEM, X-ray photoelectron spectroscopy (XPS, electron paramagnetic resonance (EPR, photoluminescence spectroscopy (PLS, and UV-Vis diffuse reflectance spectra (DRS. The results indicate that the optical properties of F-Fe-TiO2 with the {001} facet and cuboid morphology were obviously improved and its photocatalytic activity was significantly enhanced. The bromate solution of 100 μg/L was thoroughly removed with 0.5 g/L dosage of 1.0% F- and 0.08% Fe-codoped TiO2 composite within 1 hour under visible light.

  15. Potassium bromate treatment predominantly causes large deletions, but not GC > TA transversion in human cells

    Energy Technology Data Exchange (ETDEWEB)

    Luan, Yang [Div. of Cellular and Gene Therapy Products, National Inst. of Health Sciences, 1-18-1 Kamiyoga, Setagaya-ku, Tokyo 158-8501 (Japan)]|[Div. of Genetics and Mutagenesis, National Inst. of Health Sciences, 1-18-1 Kamiyoga, Setagaya-ku, Tokyo 158-8501 (Japan)]|[Center for Drug Safety Evaluation, Shanghai Inst. of Materia Medica, Chinese Academy of Sciences, 294 Tai-Yuan Road, Shanghai 200031 (China); Suzuki, Takayoshi [Div. of Cellular and Gene Therapy Products, National Inst. of Health Sciences, 1-18-1 Kamiyoga, Setagaya-ku, Tokyo 158-8501 (Japan); Palanisamy, Rajaguru [Div. of Cellular and Gene Therapy Products, National Inst. of Health Sciences, 1-18-1 Kamiyoga, Setagaya-ku, Tokyo 158-8501 (Japan)]|[Department of Biotechnology, School of Engineering and Technology, Bharathidasan Univ., Palkalaiperur, Tiruchirappalli 620024 (India); Takashima, Yoshio; Sakamoto, Hiroko; Sakuraba, Mayumi; Koizumi, Tomoko; Hayashi, Makoto [Div. of Genetics and Mutagenesis, National Inst. of Health Sciences, 1-18-1 Kamiyoga, Setagaya-ku, Tokyo 158-8501 (Japan); Saito, Mika [Div. of Genetics and Mutagenesis, National Inst. of Health Sciences, 1-18-1 Kamiyoga, Setagaya-ku, Tokyo 158-8501 (Japan)]|[Dept. of Food Science and Technology, College of Bioresource Sciences, Nihon Univ., 1866 Kameino, Fujisawa-shi, Kanagawa 252-8510 (Japan); Matsufuji, Hiroshi; Yamagata, Kazuo [Dept. of Food Science and Technology, College of Bioresource Sciences, Nihon Univ., 1866 Kameino, Fujisawa-shi, Kanagawa 252-8510 (Japan); Yamaguchi, Teruhide [Div. of Cellular and Gene Therapy Products, National Inst. of Health Sciences, 1-18-1 Kamiyoga, Setagaya-ku, Tokyo 158-8501 (Japan); Honma, Masamitsu [Div. of Genetics and Mutagenesis, National Inst. of Health Sciences, 1-18-1 Kamiyoga, Setagaya-ku, Tokyo 158-8501 (Japan)]. E-mail: honma@nihs.go.jp

    2007-06-01

    Potassium bromate (KBrO{sub 3}) is strongly carcinogenic in rodents and mutagenic in bacteria and mammalian cells in vitro. The proposed genotoxic mechanism for KBrO{sub 3} is oxidative DNA damage. KBrO{sub 3} can generate high yields of 8-hydroxydeoxyguanosine (8OHdG) DNA adducts, which cause GC > TA transversions in cell-free systems. In this study, we investigated the in vitro genotoxicity of KBrO{sub 3} in human lymphoblastoid TK6 cells using the comet (COM) assay, the micronucleus (MN) test, and the thymidine kinase (TK) gene mutation assay. After a 4 h treatment, the alkaline and neutral COM assay demonstrated that KBrO{sub 3} directly yielded DNA damages including DNA double strand breaks (DSBs). KBrO{sub 3} also induced MN and TK mutations concentration-dependently. At the highest concentration (5 mM), KBrO{sub 3} induced MN and TK mutation frequencies that were over 30 times the background level. Molecular analysis revealed that 90% of the induced mutations were large deletions that involved loss of heterozygosity (LOH) at the TK locus. Ionizing-irradiation exhibited similar mutational spectrum in our system. These results indicate that the major genotoxicity of KBrO{sub 3} may be due to DSBs that lead to large deletions rather than to 8OHdG adducts that lead to GC > TA transversions, as is commonly believed. To better understand the genotoxic mechanism of KBrO{sub 3}, we analyzed gene expression profiles of TK6 cells using Affymetrix Genechip. Some genes involved in stress, apoptosis, and DNA repair were up-regulated by the treatment of KBrO{sub 3}. However, we could not observe the similarity of gene expression profile in the treatment of KBrO{sub 3} to ionizing-irradiation as well as oxidative damage inducers.

  16. Isolation and growth characterization of chlorate and/or bromate resistant mutants generated by spontaneous and induced foreword mutations at several gene loci in aspergillus niger

    Science.gov (United States)

    Kanan, Ghassan J. M.; Al-Najjar, Heyam E.

    2010-01-01

    We aimed her mainly to evaluate the contribution of newly employed bromate selection system, in obtaining new Aspergillus niger nitrate/nitrite assimilation defective mutants, through Ultraviolet treatment (UV), 1, 2, 7, 8-Diepoxyoctane (DEO), phenols mixture (Phx)) and spontaneous treatments. The newly employed bromate selection system was able to specify only two putative novel mutant types designated brn (bromate resistant but chlorate sensitive (RS) strain, which may specify nitrite specific transporter) and cbrn mutants (bromate resistant and chlorate resistant strain, which may specify nitrate/nitrite bispecific system). The most relevant and innovative findings of this research work involve the isolation of the RR ( cbrn) mutants (a new type of nitrate assimilation defective mutants), that could be useful for studying the bispecific nitrate /nitrite transporter system. The majority of obtained bromate resistant mutants (93.3% of the total mutants obtained by all treatments) were of the brn type, whereas the remaining percentage (6.76%) was given to cbrn strains. The highest percentages of brn mutant strains (48% and 58.6% of the total RS strains) were obtained with UA after spontaneous and Phx treatment, whereas Trp has generated 29% and 42% of RS strains after UV and DEO treatments, respectively. The obtained ratios of cbrn mutants were higher (i.e. in the range of 8.4%-11.64% of the total bromate mutants) with chemical treatments, especially when U.A or Pro was serving as sole N-sources at 25ºC rather than 37ºC. A 69% mutants` yield of Aspergillus niger mutant strains representing nine gene loci ( niaD, cnx-6 loci , nrt and nirA) were selected on the bases of chlorate (600 mM) toxicity. All chlorate resistant mutants were completely sensitive to bromate (250 mM). The niaD mutants showed the highest percentage (73.97%) of chlorate resistant mutants obtained with all tested treatments. The UV treatment has generated the highest ratio (86.9%) of nia

  17. Isolation and growth characterization of chlorate and/or bromate resistant mutants generated by spontaneous and induced foreword mutations at several gene loci in Aspergillus niger

    Directory of Open Access Journals (Sweden)

    Ghassan J. M. Kanan

    2010-12-01

    Full Text Available We aimed her mainly to evaluate the contribution of newly employed bromate selection system, in obtaining new Aspergillus niger nitrate/nitrite assimilation defective mutants, through Ultraviolet treatment (UV, 1, 2, 7, 8-Diepoxyoctane (DEO, phenols mixture (Phx and spontaneous treatments. The newly employed bromate selection system was able to specify only two putative novel mutant types designated brn (bromate resistant but chlorate sensitive (RS strain, which may specify nitrite specific transporter and cbrn mutants (bromate resistant and chlorate resistant strain, which may specify nitrate/nitrite bispecific system. The most relevant and innovative findings of this research work involve the isolation of the RR (cbrn mutants (a new type of nitrate assimilation defective mutants, that could be useful for studying the bispecific nitrate /nitrite transporter system. The majority of obtained bromate resistant mutants (93.3% of the total mutants obtained by all treatments were of the brn type, whereas the remaining percentage (6.76% was given to cbrn strains. The highest percentages of brn mutant strains (48% and 58.6% of the total RS strains were obtained with UA after spontaneous and Phx treatment, whereas Trp has generated 29% and 42% of RS strains after UV and DEO treatments, respectively. The obtained ratios of cbrn mutants were higher (i.e. in the range of 8.4%-11.64% of the total bromate mutants with chemical treatments, especially when U.A or Pro was serving as sole N-sources at 25ºC rather than 37ºC. A 69% mutants' yield of Aspergillus niger mutant strains representing nine gene loci (niaD, cnx-6 loci, nrt and nirA were selected on the bases of chlorate (600 mM toxicity. All chlorate resistant mutants were completely sensitive to bromate (250 mM. The niaD mutants showed the highest percentage (73.97% of chlorate resistant mutants obtained with all tested treatments. The UV treatment has generated the highest ratio (86.9% of niaD mutants

  18. Phosphomolybdate-doped-poly(3,4-ethylenedioxythiophene) coated gold nanoparticles: Synthesis, characterization and electrocatalytic reduction of bromate

    Energy Technology Data Exchange (ETDEWEB)

    Hassan, Syeda Sara [School of Chemistry, Monash University, VIC 3800 (Australia); National Center of Excellence in Analytical Chemistry, University of Sindh, Jamshoro 76080 (Pakistan); Liu, Yuping [School of Chemistry, Monash University, VIC 3800 (Australia); Sirajuddin,; Solangi, Amber Rehana [National Center of Excellence in Analytical Chemistry, University of Sindh, Jamshoro 76080 (Pakistan); Bond, Alan M., E-mail: alan.bond@monash.edu [School of Chemistry, Monash University, VIC 3800 (Australia); Zhang, Jie, E-mail: jie.zhang@monash.edu [School of Chemistry, Monash University, VIC 3800 (Australia)

    2013-11-25

    Graphical abstract: -- Highlights: •Stable and water soluble phosphomolybdate-doped-PEDOT coated gold nanoparticles were synthesized. •Electrodes modified with these nanoparticles show well defined voltammetric response and excellent stability in acidic media. •These nanocomposite catalysts exhibit an excellent catalytic activity towards electroreduction of bromate. -- Abstract: Phosphomolybdate, H{sub 3}PMo{sub 12}O{sub 40}, (PMo{sub 12})-doped-poly(3,4-ethylenedioxythiophene) (PEDOT) coated gold nanoparticles have been synthesized in aqueous solution by reduction of AuCl{sub 4}{sup −} using hydroxymethyl EDOT as a reducing agent in the presence of polystyrene sulfonate and PMo{sub 12}. The resulting PMo{sub 12}-doped-PEDOT stabilized Au nanoparticles are water soluble and have been characterized by UV–visible spectroscopy, scanning electron microscopy and electrochemistry. Glassy carbon electrodes modified with these Au nanoparticles show excellent stability and catalytic activity towards the reduction of bromate in an aqueous electrolyte solution containing 10 mM H{sub 2}SO{sub 4} and 0.1 M Na{sub 2}SO{sub 4}.

  19. Oscillatory dynamics in systems containing bromate and 1,4-cyclohexanedione in acidic media. I. The effect of temperature; Dinamica oscilatoria em sistemas contendo bromato e 1,4-ciclo-hexanodiona em meio acido. I. Efeito da temperatura

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira, Hyrla C.L.; Oliveira, Tatiane B.; Varela, Hamilton, E-mail: varela@iqsc.usp.br [Instituto de Quimica de Sao Carlos, Universidade de Sao Paulo (IQSC/USP), Sao Carlos, SP (Brazil)

    2012-07-01

    We present in this work the influence of temperature on the dynamics of homogeneous chemical systems containing bromate and 1,4-cyclohexanedione (1,4-CHD) in acidic media. In particular, the following systems were studied: bromate/1,4-CHD/acid, bromate/1,4-CHD/ferroin/acid and bromate/1,4-CHD/trisbipyridine ruthenium/acid. Investigations were carried out by means of an electrochemical probe, at five temperatures between 5 and 45 degree C. Activation energies (Ea) were estimated in different ways for the pre-oscillatory and oscillatory regimes. In any case, the Ea was found to depend on the catalyst, composition and initial concentrations. In addition, it was observed that ferroin and trisbipyridine ruthenium act as catalysts only during the transition between the induction period and oscillatory regime. (author)

  20. Catálise eletroquímica da redução do bromato em superfícies modificadas por filmes de molibdênio Catalysis of the bromate reduction at a molybdenum oxide modified electrode

    Directory of Open Access Journals (Sweden)

    Mauro Bertotti

    1998-04-01

    Full Text Available In this paper some studies concerning the electroreduction of Mo(VI in sulphuric acid solutions are described. We have shown that at suitable experimental conditions very stable molybdenum oxide films can be electrochemically deposited at glassy carbon electrodes, the reduction of bromate occurring at less negative potentials on the modified surface. Coulometric experiments have shown that bromide is not the only product of the catalytic bromate reduction by the molybdenum film and species like BrO2 may have part in this process. Based on chronoamperometric curves recorded at -0.60 V, analytical curves have been obtained for the reduction of bromate in the 0.1 - 0.8 mM range, a limit of detection of 20 µM for bromate being determined.

  1. Epigenetic changes in p21 expression in renal cells after exposure to bromate.

    Science.gov (United States)

    Scholpa, N E; Zhang, X; Kolli, R T; Cummings, B S

    2014-10-01

    This study tested the hypothesis that bromate (KBrO3)-induced renal cell death is mediated by epigenetic mechanisms. Global DNA methylation, as assessed by 5-methylcytosine staining, was not changed in normal rat kidney cells treated with acute cytotoxic doses of KBrO3 (100 and 200 ppm), as compared with controls. However, KBrO3 treatment did increase p38, p53 and histone 2AX (H2AX) phosphorylation, and p21 expression. Treatment of cells with inhibitors of DNA methyltransferase (5-azacytidine or 5-Aza) and histone deacetylase (trichostatin A or TSA) in addition to KBrO3 increased cytotoxicity, as compared with cells exposed to KBrO3 alone. 5-Aza and TSA co-treatment did not alter p38 or p53 phosphorylation, but slightly decreased H2AX phosphorylation and significantly decreased p21 expression. We also assessed epigenetic changes in cells treated under sub-chronic conditions with environmentally relevant concentrations of KBrO3. Under these conditions (0-10ppm KBrO3 for up to 18 days), we detected no increases in cell death or DNA damage. In contrast, slight alterations were detected in the phosphorylation of H2AX, p38, and p53. Sub-chronic low-dose KBrO3 treatment also induced a biphasic response in p21 expression, with lower concentrations increasing expression, but higher concentrations decreasing expression. Methylation-specific PCR demonstrated that sub-chronic KBrO3 treatment altered the methylation of cytosine bases in the p21 gene, as compared with controls, correlating to alterations in p21 protein expression. Collectively, these data show the novel finding that KBrO3-induced renal cell death is altered by inhibitors of epigenetic modifying enzymes and that KBrO3 itself induces epigenetic changes in the p21 gene. © The Author 2014. Published by Oxford University Press on behalf of the Society of Toxicology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

  2. Application of UV absorbance and fluorescence indicators to assess the formation of biodegradable dissolved organic carbon and bromate during ozonation.

    Science.gov (United States)

    Li, Wen-Tao; Cao, Meng-Jie; Young, Tessora; Ruffino, Barbara; Dodd, Michael; Li, Ai-Min; Korshin, Gregory

    2017-03-15

    This study examined the significance of changes of UV absorbance and fluorescence of dissolved organic matter (DOM) as surrogate indicators for assessing the formation of bromate and biodegradable dissolved organic carbon (BDOC) during the ozonation of surface water and wastewater effluent. Spectroscopic monitoring was carried out using benchtop UV/Vis and fluorescence spectrophotometers and a newly developed miniature LED UV/fluorescence sensor capable of rapidly measuring UVA280 and protein-like and humic-like fluorescence. With the increase of O3/DOC mass ratio, the plots of BDOC formation were characterized of initial lag, transition slope and final plateau. With the decrease of UV absorbance and fluorescence, BDOC concentrations initially increased slowly and then rose more noticeably. Inflection points in plots of BDOC versus changes of spectroscopic indicators were close to 35-45% loss of UVA254 or UVA280 and 75-85% loss of humic-like fluorescence. According to the data from size exclusion chromatography (SEC) with organic carbon detection and 2D synchronous correlation analyses, DOM fractions assigned to operationally defined large biopolymers (apparent molecular weight, AMW>20 kDa) and medium AMW humic substances (AMW 5.5-20 kDa) were transformed into medium-size building blocks (AMW 3-5.5 kDa) and other smaller AMW species (AMWbromate formation was observed only after the values of UVA254, UVA280 and humic-like fluorescence in O3-treated samples were decreased by 45-55%, 50-60% and 86-92% relative to their respective initial levels. No significant differences in plots of bromate concentrations versus decreases of humic-like fluorescence were observed for surface water and wastewater effluent samples. This was in contrast with the plots of bromate concentration versus UVA254 and UVA280 which exhibited sensitivity to varying initial bromide concentrations in the investigated water matrixes. These results suggest that measurements of humic

  3. Development of a miniature dielectric barrier discharge–optical emission spectrometric system for bromide and bromate screening in environmental water samples

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Yong-Liang [Department of Chemistry, College of Sciences, Northeastern University, Box 332, Shenyang 110819 (China); Research Center for Analytical Sciences, College of Sciences, Northeastern University, Box 332, Shenyang 110819 (China); Cai, Yi [Research Center for Analytical Sciences, College of Sciences, Northeastern University, Box 332, Shenyang 110819 (China); Chen, Ming-Li, E-mail: chenml@mail.neu.edu.cn [Research Center for Analytical Sciences, College of Sciences, Northeastern University, Box 332, Shenyang 110819 (China); Wang, Jian-Hua, E-mail: jianhuajrz@mail.neu.edu.cn [Research Center for Analytical Sciences, College of Sciences, Northeastern University, Box 332, Shenyang 110819 (China); Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300071 (China)

    2014-01-27

    Graphical abstract: -- Highlights: •Dielectric barrier discharge (DBD) is for the first time used as a radiation source for the excitation of bromine and its emission. •A DBD–optical emission spectrometric (OES) system was developed for the detection of bromide and bromate. •The DBD–OES system has been demonstrated by screening trace bromide and bromate in a series of environmental water samples. -- Abstract: Dielectric barrier discharge (DBD) at atmospheric pressure provides an efficient radiation source for the excitation of bromine and it is used for the first time for optical emission spectrometric (OES) detection of bromide and bromate. A portable DBD–OES system is developed for screening potential pollution from bromide and bromate in environmental waters. Bromide is on-line oxidized to bromine for in-situ generation of volatile bromine. Meanwhile, a helium stream carries bromine into the DBD micro-plasma for its excitation at a discharging voltage of 3.7 kV and optical emission spectrometric detection with a QE65000 charge-coupled device (CCD) spectrometer in the near-infrared spectral region. Similarly, the quantification of bromate is performed by its pre-reduction into bromide and then oxidized to bromine. The spectral characteristics and configuration of the DBD micro-plasma excitation source in addition to the oxidation vapor generation of bromine have been thoroughly investigated. With a sampling volume of 1 mL, a linear range of 0.05–10.0 mg L{sup −1} is obtained with a detection limit of 0.014 mg L{sup −1} by measuring the emission at 827 nm. A precision of 2.3% is achieved at 3 mg L{sup −1} bromide. The system is validated by bromine detection in certified reference material of laver (GBW10023) at mg L{sup −1} level, giving rise to satisfactory agreement. In addition, it is further demonstrated by screening trace bromide and bromate as well as spiking recoveries in a series of environmental water samples.

  4. Non-chromate deoxidation of AA2024-T3: Sodium bromate nitric acid (20 60 °C)

    Science.gov (United States)

    Harvey, T. G.; Hughes, A. E.; Hardin, S. G.; Nikpour, T.; Toh, S. K.; Boag, A.; McCulloch, D.; Horne, M.

    2008-03-01

    The effect of a non-chromate deoxidiser (bromate-nitric acid) on AA2024-T3 has been examined by SEM, TEM/EELS and XPS. At low temperatures (20 °C) the deoxidiser removed all intermetallics but had little effect on the surface oxide. At 40 °C, attack on the intermetallics was again extensive but there was also evidence of attack on the surface oxide covering the matrix after 10 min of immersion, leaving a roughened porous oxide. At 60 °C, removal of intermetallics was complete and longer immersion times resulted in a characteristic scalloped structure across the surface which became more pronounced with increasing immersion time.

  5. Phase diagram and complex patterns in the modeling of the bromate-oxalic acid-Ce-acetone oscillating reaction

    Directory of Open Access Journals (Sweden)

    Janaina A. M. Pereira

    2007-06-01

    Full Text Available Simulations have been carried out on the bromate - oxalic acid - Ce(IV - acetone oscillating reaction, under flow conditions, using Field and Boyd's model (J. Phys. Chem. 1985, 89, 3707. Many different complex dynamic behaviors were found, including simple periodic oscillations, complex periodic oscillations, quasiperiodicity and chaos. Some of these complex oscillations can be understood as belonging to a Farey sequence. The many different behaviors were systematized in a phase diagram which shows that some regions of complex patterns were nested with one inside the other. The existence of almost all known dynamic behavior for this system allows the suggestion that it can be used as a model for some very complex phenomena that occur in biological systems.

  6. Potassium bromate, a potent DNA oxidizing agent, exacerbates germline repeat expansion in a Fragile X premutation mouse model

    Science.gov (United States)

    Entezam, A.; Lokanga, A. R.; Le, W.; Hoffman, G.; Usdin, K.

    2010-01-01

    Tandem repeat expansion is responsible for the Repeat Expansion Diseases, a group of human genetic disorders that includes Fragile X syndrome. FXS results from expansion of a premutation (PM) allele having 55–200 CGG•CCG-repeats in the 5’ UTR of the FMR1 gene. The mechanism of expansion is unknown. We have treated FX PM mice with potassium bromate (KBrO3), a potent DNA oxidizing agent. We then monitored the germline and somatic expansion frequency in the progeny of these animals. We show here that KBrO3 increased both the level of 8-oxoG in the oocytes of treated animals and the germline expansion frequency. Our data thus suggest that oxidative damage may be a factor that could affect expansion risk in humans. PMID:20213777

  7. The catalytic kinetic method for the determination of trace formaldehyde (FA) base on a bromate-eosin Y system

    Science.gov (United States)

    Tang, Yufang; Chen, Hao; Weng, Chao; Tang, Xiaohui; Zhang, Miaoling; Yang, Qiongqiong; Hu, Tao; Cai, Changqun

    A new simple and highly sensitive catalytic kinetic method for the determination of trace amount of FA in food sample has been established. The method was based on the catalytic effect of FA on the oxidation of eosin Y by potassium bromate in present of phosphoric acid. The reaction was monitored spectrophotometrically by measuring the decrease in absorbance of eosin Y at 518 nm. Under the optimized experimental conditions, the developed method allowed the determination of FA in the range of 0.03-0.6 μg mL-1 with a good precision, and the limit of detection was down to 0.00988 μg mL-1. The relative standard deviation of five replicate measurements for the determination of FA in concentration 0.12 μg mL-1 was 1.8%. The proposed method was successfully applied to the determination of FA in food directly and satisfactory results were obtained.

  8. Catalytic kinetic spectrophotometric determination of trace titanium based on titanium(IV-(DBS-arsenazo-potassium bromate system

    Directory of Open Access Journals (Sweden)

    Qing-Zhou Zhai

    2007-04-01

    Full Text Available Based on the property that in 0.12 M sulfuric acid medium titanium(IV catalyzes the discoloring reaction of DBS-arsenazo oxidized by potassium bromate, a new catalytic kinetic spectrophotometric method for the determination of trace titanium (IV was developed. The linear range of the determination of titanium is 0-2.4 μg/25 mL. The detection limit of the method is 0.47 ng/mL. The effects of fifty coexisting substances were studied and most of common substances do not interfere with the determination of titanium. The method has good selectivity. The present method was used in the determination of trace amount of titanium in cabbage and potato samples with satisfactory results. The relative standard deviations of ten replicate determinations of the method are 1.4-1.5 % and the recoveries of standard addition are 97.6-98.0 %, respectively.

  9. Catalytic Spectrophotometric Method for Determination of Formaldehyde Based on its Catalytic Effect on the ReactionBetween Bromate and Safranin

    Directory of Open Access Journals (Sweden)

    Mohsen Keyvanfard

    2010-01-01

    Full Text Available The reaction monitored spectrophotometrically by measuring the decrease in absorbance of the reaction mixture at 533 nm. The fixed-time method was used for the first 60s. For initiation of the reaction, under the optimum conditions, in the concentration range of 0.02-1.5 μg mL–1 formaldehyde can be determined with a limit of detection 9.5 ng mL–1. The relative standard deviation of five replicate measurements is 2.3% for 0.5 μg mL–1 of formaldehyde. The method was used for the determination of formaldehyde in water samples with satisfactory results. A new simple and fast catalytic kinetic method for the determination of trace amount of formaldehyde is described. The method is based on the catalytic effect of formaldehyde on the oxidation of safranin by bromate in the present of sulfuric acid.

  10. Analysis of haloacetic acids, bromate, and dalapon in natural waters by ion chromatography-tandem mass spectrometry.

    Science.gov (United States)

    Wu, Shimin; Anumol, Tarun; Gandhi, Jay; Snyder, Shane A

    2017-03-03

    The addition of oxidants for disinfecting water can lead to the formation of potentially carcinogenic compounds referred to as disinfection byproducts (DBPs). Haloacetic acids (HAAs) are one of the most widely detected DBPs in US water utilities and some of them are regulated by the US Environmental Protection Agency (USEPA). The present study developed a method to analyze all the compounds in the USEPA method 557 (nine HAAs, bromate and dalapon) plus four potentially more toxic iodinated HAAs in water by coupling ion chromatography with tandem mass spectrometry (IC-MS/MS). This aqueous direct injection method has significant advantages over traditional GC methods, which require a derivatization and sample extraction that are laborious, time-consuming, and can negatively impact reproducibility. The method developed in this study requires half the time of the current USEPA method 557 on IC-MS/MS while including more compounds and achieving sub-μg/L level method detection limits (MDLs) for all 15 target analytes. The single laboratory lowest concentration minimum reporting level (LCMRL) has also been determined in reagent water, which ranged from 0.011 to 0.62μg/L for the analytes. The mean recoveries of the analytes during matrix spike recovery tests were 77-125% in finished drinking water and 81-112% in surface water. This method was then applied to untreated, chlorinated, and chloraminated groundwater and surface water samples. Bromate and 9 HAAs were detected at different levels in some of these samples. Copyright © 2017 Elsevier B.V. All rights reserved.

  11. The indirect effect of radiation reduces the repair fidelity of NHEJ as verified in repair deficient CHO cell lines exposed to different radiation qualities and potassium bromate

    Energy Technology Data Exchange (ETDEWEB)

    Bajinskis, Ainars, E-mail: ainars.bajinskis@gmt.su.se [Centre for Radiation Protection Research, Department of Genetics, Microbiology and Toxicology, Stockholm University, S-10691 Stockholm (Sweden); Olsson, Gunilla; Harms-Ringdahl, Mats [Centre for Radiation Protection Research, Department of Genetics, Microbiology and Toxicology, Stockholm University, S-10691 Stockholm (Sweden)

    2012-03-01

    The complexity of DNA lesions induced by ionizing radiation is mainly dependent on radiation quality, where the indirect action of radiation may contribute to different extent depending on the type of radiation under study. The effect of indirect action of radiation can be investigated by using agents that induce oxidative DNA damage or by applying free radical scavengers. The aim of this study was to investigate the role of the indirect effect of radiation for the repair fidelity of non-homologous end-joining (NHEJ), homologous recombination repair (HRR) and base excision repair (BER) when DNA damage of different complexity was induced by gamma radiation, alpha particles or from base damages (8-oxo-dG) induced by potassium bromate (KBrO{sub 3}). CHO cells lines deficient in XRCC3 (HRR) irs1SF, XRCC7 (NHEJ) V3-3 and XRCC1 (BER) EM9 were irradiated in the absence or presence of the free radical scavenger dimethyl sulfoxide (DMSO). The endpoints investigated included rate of cell proliferation by the DRAG assay, clonogenic cell survival and the level of primary DNA damage by the comet assay. The results revealed that the indirect effect of low-LET radiation significantly reduced the repair fidelity of both NHEJ and HRR pathways. For high-LET radiation the indirect effect of radiation also significantly reduced the repair fidelity for the repair deficient cell lines. The results suggest further that the repair fidelity of the error prone NHEJ repair pathway is more impaired by the indirect effect of high-LET radiation relative to the other repair pathways studied. The response to bromate observed for the two DSB repair deficient cell lines strongly support earlier studies that bromate induces complex DNA damages. The significantly reduced repair fidelity of irs1SF and V3-3 suggests that NHEJ as well as HRR are needed for the repair, and that complex DSBs are formed after bromate exposure.

  12. Sensitive and rapid titrimetric and spectrophotometric methods for the determination of stavudine in pharmaceuticals using bromate-bromide and three dyes.

    Science.gov (United States)

    Basavaiah, Kanakapura; Ramakrishna, Veeraiah; Somashekar, Chikkaswamy; Kumar, Urdigere R Anil

    2008-06-01

    Four sensitive and rapid methods for the determination of stavudine (STV) in bulk drug and in dosage forms were developed and optimized. In titrimetry, aqueous solution of STV was treated with a known excess of bromate-bromide in HCl medium followed by estimation of unreacted bromine by iodometric back titration. Spectrophotometric methods involve the addition of a measured excess of bromate-bromide in HCl medium and subsequent estimation of the residual bromine by reacting with a fixed amount of methyl orange, indigocarmine or thymol blue followed by measurement of absorbance at 520 nm (method A), 610 nm (method B) or 550 nm (method C). In all the methods, the amount of bromate reacted corresponds to the amount of STV. Calculations in titrimetry were based on a 1:0.666 (STV:KBrO3) stoichiometry and the method was found to be applicable over 3.5-10 mg range. A linear increase in absorbance with concentration of STV was observed in the spectrophotometric methods, and the Beer's law was obeyed over the concentration ranges 0.125-1.75, 1-10 and 1-9.0 microg mL-1 STV for method A, method B and method C, respectively. The methods when applied to the determination of STV in tablets and capsules were found to give satisfactory results.

  13. Cisapride a green analytical reagent for rapid and sensitive determination of bromate in drinking water, bread and flour additives by oxidative coupling spectrophotometric methods

    Science.gov (United States)

    Al Okab, Riyad Ahmed

    2013-02-01

    Green analytical methods using Cisapride (CPE) as green analytical reagent was investigated in this work. Rapid, simple, and sensitive spectrophotometric methods for the determination of bromate in water sample, bread and flour additives were developed. The proposed methods based on the oxidative coupling between phenoxazine and Cisapride in the presence of bromate to form red colored product with max at 520 nm. Phenoxazine and Cisapride and its reaction products were found to be environmentally friendly under the optimum experimental condition. The method obeys beers law in concentration range 0.11-4.00 g ml-1 and molar absorptivity 1.41 × 104 L mol-1 cm-1. All variables have been optimized and the presented reaction sequences were applied to the analysis of bromate in water, bread and flour additive samples. The performance of these method was evaluated in terms of Student's t-test and variance ratio F-test to find out the significance of proposed methods over the reference method. The combination of pharmaceutical drugs reagents with low concentration create some unique green chemical analyses.

  14. Sensitive and robotic determination of bromate in sea water and drinking deep-sea water by headspace solid-phase micro extraction and gas chromatography-mass spectrometry.

    Science.gov (United States)

    Lim, Hyun-Hee; Shin, Ho-Sang

    2012-09-05

    A robotic method has been established for the determination of bromate in sea water and drinking deep-sea water. Bromate in water was converted into volatile derivative, which was measured with headspace solid-phase micro extraction and gas chromatography-mass spectrometry (HS-SPME GC-MS). Derivatization reagent and the HS-SPME parameters (selection of fibre, extraction/derivatization temperature, heating time and; the morality of HCl) were optimized and selected. Under the established conditions, the detection and the quantification limits were 0.016 μg L(-1) and 0.051 μg L(-1), respectively, and the intra- and inter-day relative standard deviation was less than 7% at concentrations of 1.0 and 10.0 μg L(-1). The calibration curve showed good linearity with r(2)=0.9998. The common ions Cl(-), NO(3)(-), SO(4)(2-), HPO(4)(2-), H(2)PO(4)(-), K(+), Na(+), NH(4)(+), Ca(2+), Mg(2+), Ba(2+), Mn(4+), Mn(2+), Fe(3+) and Fe(2+) did not interfere even when present in 1000-fold excess over the active species. The method was successfully applied to the determination of bromate in sea water and drinking deep-sea water. Copyright © 2012 Elsevier B.V. All rights reserved.

  15. 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.

  16. Oxyhalogen-sulfur chemistry: kinetics and mechanism of oxidation of N-acetyl homocysteine thiolactone by acidified bromate and aqueous bromine.

    Science.gov (United States)

    Mbiya, Wilbes; Choi, Boyoung; Martincigh, Bice S; Morakinyo, Moshood K; Simoyi, Reuben H

    2013-12-12

    N-acetyl homocysteine thiolactone (NAHT), medically known as citiolone, can be used as a mucolytic agent and for the treatment of certain hepatic disorders. We have studied the kinetics and mechanisms of its oxidation by acidic bromate and aqueous bromine. In acidic bromate conditions the reaction is characterized by a very short induction period followed by a sudden and rapid formation of bromine and N-acetyl homocysteine sulfonic acid. The stoichiometry of the bromate-NAHT reaction was deduced to be: BrO3(-) + H2O + CH3CONHCHCH2CH2SCO → CH3CONHCHCH2CH2(SO3H)COOH + Br(-) (S1) while in excess bromate it was deduced to be: 6BrO3(-) + 5CH3CONHCHCH2CH2SCO + 6H(+) → 3Br2 + 5CH3CONHCHCH2CH2(SO3H)COOH + 2H2O (S2). For the reaction of NAHT with bromine, a 3:1 stoichiometric ratio of bromine to NAHT was obtained: 3Br2 + CH3CONHCHCH2CH2SCO + 4H2O → 6Br(-) + CH3CONHCHCH2CH2(SO3H)COOH + 6H(+) (S3). Oxidation occurred only on the sulfur center where it was oxidized to the sulfonic acid. No sulfate formation was observed. The mechanism involved an initial oxidation to a relatively stable sulfoxide without ring-opening. Further oxidation of the sulfoxide involved two pathways: one which involved intermediate formation of an unstable sulfone and the other involves ring-opening coupled with oxidation through to the sulfonic acid. There was oligooscillatory production of aqueous bromine. Bromide produced in S1 reacts with excess bromate to produce aqueous bromine. The special stability associated with the sulfoxide allowed it to coexist with aqueous bromine since its further oxidation to the sulfone was not as facile. The direct reaction of aqueous bromine with NAHT was fast with an estimated lower limit bimolecular rate constant of 2.94 ± 0.03 × 10(2) M(-1) s(-1).

  17. Thionine-Bromate as a New Reaction System for Kinetic Spectrophotometric Determination of Hydrazine in Cooling Tower Water Samples

    Directory of Open Access Journals (Sweden)

    Masoud Reza Shishehbore

    2013-01-01

    Full Text Available A simple, selective, and inexpensive kinetic method was developed for the determination of hydrazine based on its inhibitory effect on the thionine-bromate system in sulfuric acid media. The reaction was monitored spectrophotometrically at 601 nm by a fixed time method. The effect of different parameters such as concentration of reactants, ionic strength, temperature, and time on the rate of reaction was investigated, and the optimum conditions were obtained. Under optimum conditions, the calibration curve was linear in the concentration range from 0.8–23.0 μg mL−1 of hydrazine, and the detection limit of the method was 0.22 μg mL−1. The relative standard deviation for five replicate determinations of 1.0 μg mL−1 of hydrazine was 0.74%. The potential of interfering effect of foreign species on the hydrazine determination was studied. The proposed method was successfully applied for the determination of hydrazine in different water samples.

  18. An overview of advanced reduction processes for bromate removal from drinking water: Reducing agents, activation methods, applications and mechanisms.

    Science.gov (United States)

    Xiao, Qian; Yu, Shuili; Li, Lei; Wang, Ting; Liao, Xinlei; Ye, Yubing

    2017-02-15

    Bromate (BrO 3 - ) is a possible human carcinogen regulated at a strict standard of 10μg/L in drinking water. Various techniques to eliminate BrO 3 - usually fall into three main categories: reducing bromide (Br - ) prior to formation of BrO 3 - , minimizing BrO 3 - formation during the ozonation process, and removing BrO 3 - from post-ozonation waters. However, the first two approaches exhibit low degradation efficiency and high treatment cost. The third workaround has obvious advantages, such as high reduction efficiency, more stable performance and easier combination with UV disinfection, and has therefore been widely implemented in water treatment. Recently, advanced reduction processes (ARPs), the photocatalysis of BrO 3 - , have attracted much attention due to improved performance. To increase the feasibility of photocatalytic systems, the focus of this work concerns new technological developments, followed by a summary of reducing agents, activation methods, operational parameters, and applications. The reaction mechanisms of two typical processes involving UV/sulfite homogeneous photocatalysis and UV/titanium dioxide heterogeneous photocatalysis are further summarized. The future research needs for ARPs to reach full-scale potential in drinking water treatment are suggested accordingly. Copyright © 2016. Published by Elsevier B.V.

  19. Application of bromate-bromide mixture as a green brominating agent for the spectrophotometric determination of atenolol in pharmaceuticals

    Directory of Open Access Journals (Sweden)

    Prashanth Nagaraj Kudige

    2012-01-01

    Full Text Available Two highly sensitive spectrophotometric methods are proposed for the quantification of atenolol (ATN in pure drug as well as in pharmaceutical formulations. The methods are based on the bromination reaction of ATN with a known excess of bromate-bromide mixture in acid medium followed by the determination of unreacted bromine. The residual bromine is determined by its reaction with excess iodide and the liberated iodine (I3□ is either measured at 360 nm (method A or reacted with starch followed by the measurement of the starch-iodine chromogen at 570 nm (method B. Under the optimum conditions, ATN could be assayed in the concentration ranges of 0.5-9.0 and 0.3-6.0μg mL-1 for method A and method B, respectively, with corresponding molar absorptivity values of 2.36×104 and 2.89×104 L/mol.cm. Sandell’s sensitivity values are found to be 0.0113 and 0.0092 μg/cm2 for method A and method B, respectively. The proposed methods were successfully applied to the analysis of different commercial brands of pharmaceutical formulations and the results obtained by the proposed methods were in good agreement with those obtained using the reference method. The reliability of the methods was further ascertained by recovery studies using standard- addition method.

  20. pH-oscillations in the bromate-sulfite reaction in semibatch and in gel-fed batch reactors

    Science.gov (United States)

    Poros, Eszter; Kurin-Csörgei, Krisztina; Szalai, István; Rábai, Gyula; Orbán, Miklós

    2015-06-01

    The simplest bromate oxidation based pH-oscillator, the two component BrO3--SO32- flow system was transformed to operate under semibatch and closed arrangements. The experimental preconditions of the pH-oscillations in semibatch configuration were predicted by model calculations. Using this information as guideline large amplitude (ΔpH˜3), long lasting (11-24 h) pH-oscillations accompanied with only a 20% increase of the volume in the reactor were measured when a mixture of Na2SO3 and H2SO4 was pumped into the solution of BrO3- with a very low rate. Batch-like pH-oscillations, similar in amplitude and period time appeared when the sulfite supply was substituted by its dissolution from a gel layer prepared previously in the reactor in presence of high concentration of Na2SO3. The dissolution vs time curve and the pH-oscillations in the semibatch and closed systems were successfully simulated. Due to the simplicity in composition and in experimental technique, the semibatch and batch-like BrO3--SO32- pH-oscillators may become superior to their CSTR (continuous flow stirred tank reactor) version in some present and future applications.

  1. Biological properties of Alsidium corallinum and its potential protective effects against damage caused by potassium bromate in the mouse liver.

    Science.gov (United States)

    Ben Saad, Hajer; Kharrat, Nadia; Krayem, Najeh; Boudawara, Ons; Boudawara, Tahia; Zeghal, Najiba; Ben Amara, Ibtissem

    2016-02-01

    In the course of searching for hepatoprotective agents from natural sources, the protective effect of chemical constituents of the marine red alga Alsidium corallinum (A. corallinum) against potassium bromate (KBrO3)-induced liver damage in adult mice was investigated. The in vitro antioxidant and antibacterial properties of A. corallinum were firstly investigated. Then, A. corallinum was tested in vivo for its potential protective effects against damage caused by KBrO3 in mice models divided into four groups: controls, KBrO3, KBrO3 + A. corallinum, and A. corallinum. Our results demonstrated the rich composition of A. corallinum in antioxidant compounds like phenolics, flavonoids, anthocyanins, polysaccharides, chlorophyll and carotenoids. Its antioxidant activity was also confirmed using β-carotene bleaching by linoleic acid assay, reducing sugar test and trolox equivalent antioxidant capacity. The ethanolic extract of A. corallinum also showed good inhibition of the tested bacteria. The coadministration of the red alga associated to the KBrO3 alleviated hepatotoxicity as monitored by the improvement of hepatic oxidative stress biomarkers and plasma biochemical parameters, when compared to the KBrO3-treated mice. These results were confirmed by the improvement of histological and molecular changes. Treatment with A. corallinum prevented liver damage induced by KBrO3, thus protecting the body against free radicals and reducing inflammation and hypercholesterolemia risks.

  2. Kinetic Spectrophotometric Method for Trace Amounts Determination of Bromide in Pharmaceutical Samples Using Janus Green-Bromate System

    Directory of Open Access Journals (Sweden)

    Masoud Reza Shishehbore

    2011-01-01

    Full Text Available A new simple and rapid kinetic spectrophotometric method has been developed to trace amounts determination of bromide. This method is based on the catalytic effect of bromide on the reaction between Janus Green and bromate in sulfuric acid media. The reaction was followed spectrophotometrically by measuring the absorbance at 618 nm. The fixed-time method was used for the first 210 s. The influence of reagents concentration, temperature and time on the sensitivity was studied. Under optimum experimental conditions, bromide can be determined in the range of 10.0-1800.0 μg/L. The relative standard deviations (n = 10 were 0.22 and 0.19% for 100.0 and 1000.0 g/L of bromide, respectively. The detection limit of the proposed method was 4.1 μg/L. The influence of potential interfering of some ions and biological species on the selectivity was studied. The proposed method was successfully applied for the determination of bromide in pharmaceutical samples. The new developed method was found to have fairly good selectivity, sensitivity, simplicity and rapidity.

  3. Spectrophotometric determination of nitrite based on its catalytic effect on the reaction of nuclear fast red and potassium bromate

    Directory of Open Access Journals (Sweden)

    HASSAN ZAVVAR MOUSAVI

    2009-08-01

    Full Text Available A highly selective and sensitive catalytic spectrophotometric method was developed for the determination of nitrite in water samples. The method is based on its catalytic effect on the nuclear fast red–potassium bromate redox reaction in acidic medium. The reaction was followed spectrophotometrically by measuring the change in the absorbance at 518 nm of nuclear fast red 5 min after initiation of the reaction. In this study, the experimental parameters were optimized and the effects of other cations and anions on the determination of nitrite were examined. The calibration graph was linear in the range 2.0–45 µg mL-1 of nitrite. The relative standard deviations for the determination of 15 and 30 µg mL-1 of nitrite were 3.1 and 1.75 %, respectively (n = 8. The detection limit calculated from three times the standard deviation of the blank 3Sb was 0.7 µg mL-1. The method was successfully applied to the determination of nitrite in spiked tap, natural and wastewater samples.

  4. Oral administration of potassium bromate induces neurobehavioral changes, alters cerebral neurotransmitters level and impairs brain tissue of swiss mice.

    Science.gov (United States)

    Ajarem, Jamaan; Altoom, Naif G; Allam, Ahmed A; Maodaa, Saleh N; Abdel-Maksoud, Mostafa A; Chow, Billy Kc

    2016-05-12

    Potassium bromate (KBrO3) is widely used as a food additive and is a major water disinfection by-product. The present study reports the side effects of KBrO3 administration on the brain functions and behaviour of albino mice. Animals were divided into three groups: control, low dose KBrO3 (100 mg/kg/day) and high dose KBrO3 (200 mg/kg/day) groups. Administration of KBrO3 led to a significant change in the body weight in the animals of the high dose group in the first, second and the last weeks while water consumption was not significantly changed. Neurobehavioral changes and a reduced Neurotransmitters levels were observed in both KBrO3 groups of mice. Also, the brain level of reduced glutathione (GSH) in KBrO3 receiving animals was decreased. Histological studies favoured these biochemical results showing extensive damage in the histological sections of brain of KBrO3-treated animals. These results show that KBrO3 has serious damaging effects on the central nervous system and therefore, its use should be avoided.

  5. Vanillin mitigates potassium bromate-induced molecular, biochemical and histopathological changes in the kidney of adult mice.

    Science.gov (United States)

    Ben Saad, Hajer; Driss, Dorra; Ellouz Chaabouni, Samia; Boudawara, Tahia; Zeghal, Khaled Mounir; Hakim, Ahmed; Ben Amara, Ibtissem

    2016-05-25

    The present study aimed to explore the ability of vanillin to ameliorate the adverse effects induced by potassium bromate (KBrO3) in the renal tissue. Our results showed a significant increase in hydrogen peroxide, superoxide anion, malondialdehyde, advanced oxidation protein product and protein carbonyl levels in the kidney of KBrO3 treated mice, compared with the control group. Nephrotoxicity was evidenced by a decrease in plasma uric acid and kidney glutathione levels, Na(+)-K(+)-ATPase, lactate dehydrogenase and catalase activities. Additionally, creatinine and urea levels significantly increased in the plasma and declined in the urine. Also, Kidney glutathione peroxidase, superoxide dismutase, metallothionein (MT1 and MT2) mRNA expression remarkably increased. These modifications in biochemical and molecular values were substantiated by histopathological data. Co-treatment with vanillin restored these parameters to near control values. Interestingly, vanillin proved to possess, in vitro, a stronger scavenging radical activity than vitamin C and Trolox. Thus, vanillin inhibited KBrO3-induced damage via its antioxidant and antiradical activities as well as its capacity to protect genes expression and histopathological changes. Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.

  6. Adsorption characteristics of trace levels of bromate in drinking water by modified bamboo-based activated carbons.

    Science.gov (United States)

    Chen, Ho-Wen; Chuang, Yen Hsun; Hsu, Cheng-Feng; Huang, Winn-Jung

    2017-09-19

    This study was undertaken to investigate the adsorption kinetics and isotherms of bromate (BrO 3 - ) on bamboo charcoals that are activated with nitrogen and water vapor. Bamboo-based activated carbon (AC) was dipped in acid and oxidized in a mixture of potassium permanganate and sulfuric acid. Oxidation treatment considerably improved the physicochemical properties of AC, including purity, pore structure and surface nature, significantly enhancing BrO 3 - adsorption capacity. AC with many oxygenated groups and a high mesopore volume exhibited a particularly favorable tendency for BrO 3 - adsorption. Its adsorption of BrO 3 - is best fitted using Langmuir isotherm, and forms a monolayer. A kinetic investigation revealed that the adsorption of BrO 3 - by the ACs involved chemical sorption and was controlled by intra-particle diffusion. The competitive effects of natural organic matter (NOM) on AC were evaluated, and found to reduce the capacity of carbon to adsorb BrO 3 - . Residual dissolved ozone reacted with AC, reducing its capacity to absorb BrO 3 - . Proper dosing and staging of the ozonation processes can balance the ozone treatment efficiency, BrO 3 - formation, and the subsequent removal of BrO 3 - .

  7. The influence of the combined effects of acute gamma-radiation, sodium bromate and sodium nitrate on lettuce (Lactuca sativa) seedling root growth

    Energy Technology Data Exchange (ETDEWEB)

    Pryakhin, E.; Osipov, D. [Urals Research Center for Radiation Medicine - URCRM (Russian Federation)

    2014-07-01

    Among special industrial reservoirs used for the storage of liquid radioactive waste of Mayak PA, Russia, one of the most radioactively contaminated is the R-17 reservoir, so-called 'Staroye Boloto' (the total β-activity of water ranged in the observation period from 0.4 MBq/l to 4.5 MBq/l, the total a-activity ranged from 43 to 420 Bq/l). Also this reservoir is characterized by high level of chemical contamination, in particular, the concentration of nitrates in water is 2.5-4,4 g/l, sodium bromate - up to 35 mg/l. One of the interesting questions is interaction of radiation and chemical contamination in their effect on living organisms in this reservoir. In laboratory experiments seeds of Lactuca sativa were used; the effect of the studied factor on the length of the sprout's root was estimated. To assess the effect of chemical toxicants the solutions of each salt in 7 different concentrations were used, distilled water was used as a control. For evaluation of acute effects of external gamma irradiation the seeds after exposure for 24 hours in distilled water, were irradiated at 7 different doses using gamma-unit on the basis of Cs-137 with the dose rate of 0.62 Gy/min. To assess the combined effects of acute external gamma irradiation, of nitrates and bromates, seeds after 24 hour exposure at each test concentration of the salts solutions were irradiated using gamma-unit. To calculate the effective concentrations or doses was used drc package for R software. To calculate the dose rate to aquatic organisms in the R-17 was used ERICA Assessment Tool 2012. It was found out that the EC50 of sodium nitrate for lettuce was 2.69 g/l, which is comparable to the concentration of nitrates in the 'Staroye Boloto'. This indicates that nitrate can have significant toxic effect on aquatic higher plants of the reservoir. The EC50 of sodium bromate was 14.6 mg/l. This is less than the maximum concentration of the substance in the R-17, which suggests

  8. Reuse of sewage sludge as a catalyst in ozonation - Efficiency for the removal of oxalic acid and the control of bromate formation

    Energy Technology Data Exchange (ETDEWEB)

    Wen, Gang [State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150090 (China); Pan, Zhi-Hui [School Of Civil Engineering, Guangzhou University, Guangzhou 510006 (China); Ma, Jun, E-mail: majun@hit.edu.cn [State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150090 (China); Liu, Zheng-Qian, E-mail: liuzhengqian@gmail.com [School of Environmental Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China); Zhao, Lei [School of Civil Engineering, Harbin Institute of Technology, Harbin 150090 (China); Li, Jun-Jing [State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150090 (China)

    2012-11-15

    Highlights: Black-Right-Pointing-Pointer Sewage sludge was converted into catalyst (SBC) and characterized. Black-Right-Pointing-Pointer SBC can enhance oxalic acid degradation in ozonation. Black-Right-Pointing-Pointer Surface reaction mechanism is responsible for enhancement of ozonation by SBC. Black-Right-Pointing-Pointer SBC can control the formation of bromate in ozonation. Black-Right-Pointing-Pointer Several combined reasons for the control of bromate formation are proposed. - Abstract: Sewage derived sludge is produced with an annual amount increase of 2% all over the world and it is an urgent issue to be addressed by human being. In the present study, sludge was converted into sludge-based catalyst (SBC) with ZnCl{sub 2} as activation agent and characterized by several methods (e.g., scanning electron microscope, X-ray photoelectron spectroscope and Fourier transform infrared spectroscope). Then it was used as a catalyst to enhance the removal of refractory organic matter, oxalic acid, and to control the formation of bromate (BrO{sub 3}{sup -}) in bench semi-continuous ozonation experiments. The effects of various operating parameters on the control of BrO{sub 3}{sup -} formation were investigated. Furthermore, the mechanism for the enhancement of organic matter removal and the control of BrO{sub 3}{sup -} formation was discussed as well. Results indicate that the combination of SBC with ozone shows a strong synergistic effect, resulting in a notable improvement on oxalic acid removal. A crucial surface reaction mechanism for the enhancement of organic matter removal is proposed on the basis of negative effect of higher pH and no inhibition effect of tert-butanol. The control for BrO{sub 3}{sup -} formation was demonstrated and the reason for its control in the process of O{sub 3}/SBC is the combined effect of SBC reductive properties, ozone exposure decrease and hydrogen peroxide concentration increase.

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

    Energy Technology Data Exchange (ETDEWEB)

    Salimi, Abdollah [Department of Chemistry, University of Kurdistan, P.O. Box 416, Sanandaj (Iran, Islamic Republic of); Nanotechnology Research Center of University of Kurdistan, P.O. Box 416, Sanandaj (Iran, Islamic Republic of); E-mail: absalimi@uok.ac.ir; MamKhezri, Hussein [Department of Chemistry, University of Kurdistan, P.O. Box 416, Sanandaj (Iran, Islamic Republic of); Hallaj, Rahman [Department of Chemistry, University of Kurdistan, P.O. Box 416, Sanandaj (Iran, Islamic Republic of); Zandi, Shiva [Laboratory of Biochemistry, Kurdistan Medical University, Sanandaj (Iran, Islamic Republic of)

    2007-06-10

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

  10. The indirect effect of radiation reduces the repair fidelity of NHEJ as verified in repair deficient CHO cell lines exposed to different radiation qualities and potassium bromate.

    Science.gov (United States)

    Bajinskis, Ainars; Olsson, Gunilla; Harms-Ringdahl, Mats

    2012-03-01

    The complexity of DNA lesions induced by ionizing radiation is mainly dependent on radiation quality, where the indirect action of radiation may contribute to different extent depending on the type of radiation under study. The effect of indirect action of radiation can be investigated by using agents that induce oxidative DNA damage or by applying free radical scavengers. The aim of this study was to investigate the role of the indirect effect of radiation for the repair fidelity of non-homologous end-joining (NHEJ), homologous recombination repair (HRR) and base excision repair (BER) when DNA damage of different complexity was induced by gamma radiation, alpha particles or from base damages (8-oxo-dG) induced by potassium bromate (KBrO(3)). CHO cells lines deficient in XRCC3 (HRR) irs1SF, XRCC7 (NHEJ) V3-3 and XRCC1 (BER) EM9 were irradiated in the absence or presence of the free radical scavenger dimethyl sulfoxide (DMSO). The endpoints investigated included rate of cell proliferation by the DRAG assay, clonogenic cell survival and the level of primary DNA damage by the comet assay. The results revealed that the indirect effect of low-LET radiation significantly reduced the repair fidelity of both NHEJ and HRR pathways. For high-LET radiation the indirect effect of radiation also significantly reduced the repair fidelity for the repair deficient cell lines. The results suggest further that the repair fidelity of the error prone NHEJ repair pathway is more impaired by the indirect effect of high-LET radiation relative to the other repair pathways studied. The response to bromate observed for the two DSB repair deficient cell lines strongly support earlier studies that bromate induces complex DNA damages. The significantly reduced repair fidelity of irs1SF and V3-3 suggests that NHEJ as well as HRR are needed for the repair, and that complex DSBs are formed after bromate exposure. Copyright © 2011 Elsevier B.V. All rights reserved.

  11. Reduction of Bromate by Cobalt-Impregnated Biochar Fabricated via Pyrolysis of Lignin Using CO2 as a Reaction Medium.

    Science.gov (United States)

    Cho, Dong-Wan; Kwon, Gihoon; Ok, Yong Sik; Kwon, Eilhann E; Song, Hocheol

    2017-04-19

    In this study, pyrolysis of lignin impregnated with cobalt (Co) was conducted to fabricate a Co-biochar (i.e., Co/lignin biochar) for use as a catalyst for bromate (BrO3-) reduction. Carbon dioxide (CO2) was employed as a reaction medium in the pyrolysis to induce desired effects associated with CO2; (1) the enhanced thermal cracking of volatile organic compounds (VOCs) evolved from the thermal degradation of biomass, and (2) the direct reaction between CO2 and VOCs, which resulted in the enhanced generation of syngas (i.e., H2 and CO). This study placed main emphases on three parts: (1) the role of impregnated Co in pyrolysis of lignin in the presence of CO2, (2) the characterization of Co/lignin biochar, and (3) evaluation of catalytic capability of Co-lignin biochar in BrO3- reduction. The findings from the pyrolysis experiments strongly evidenced that the desired CO2 effects were strengthened due to catalytic effect of impregnated Co in lignin. For example, the enhanced generation of syngas from pyrolysis of Coimpregnated lignin in CO2 was more significant than the case without Co impregnation. Moreover, pyrolysis of Coimpregnated lignin in CO2 led to production of biochar of which surface area (599 m2 g-1) is nearly 100 times greater than the biochar produced in N2 (6.6 m2 g-1). Co/lignin biochar produced in CO2 also showed a great performance in catalyzing BrO3- reduction as compared to the biochar produced in N2.

  12. Association of brominated proteins and changes in protein expression in the rat kidney with subcarcinogenic to carcinogenic doses of bromate.

    Science.gov (United States)

    Kolisetty, Narendrababu; Bull, Richard J; Muralidhara, Srinivasa; Costyn, Leah J; Delker, Don A; Guo, Zhongxian; Cotruvo, Joseph A; Fisher, Jeffrey W; Cummings, Brian S

    2013-10-15

    The water disinfection byproduct bromate (BrO3(-)) produces cytotoxic and carcinogenic effects in rat kidneys. Our previous studies demonstrated that BrO3(-) caused sex-dependent differences in renal gene and protein expression in rats and the elimination of brominated organic carbon in their urine. The present study examined changes in renal cell apoptosis and protein expression in male and female F344 rats treated with BrO3(-) and associated these changes with accumulation of 3-bromotyrosine (3-BT)-modified proteins. Rats were treated with 0, 11.5, 46 and 308 mg/L BrO3(-) in drinking water for 28 days and renal sections were prepared and examined for apoptosis (TUNEL-staining), 8-oxo-deoxyguanosine (8-oxoG), 3-BT, osteopontin, Kim-1, clusterin, and p-21 expression. TUNEL-staining in renal proximal tubules increased in a dose-related manner beginning at 11.5mg BrO3(-)/L in female rats and 46 mg/L in males. Increased 8-oxoG staining was observed at doses as low as 46 mg/L. Osteopontin expression also increased in a dose-related manner after treatment with 46 mg/L, in males only. In contrast, Kim-1 expression increased in a dose-related manner in both sexes, although to a greater extent in females at the highest dose. Clusterin and p21 expression also increased in a dose-related manner in both sexes. The expression of 3-BT-modified proteins only increased in male rats, following a pattern previously reported for accumulation of α-2u-globulin. Increases in apoptosis in renal proximal tubules of male and female rats at the lowest doses suggest a common mode of action for renal carcinogenesis for the two sexes that is independent of α-2u-globulin nephropathy. © 2013.

  13. Flavonoid compounds from the red marine alga Alsidium corallinum protect against potassium bromate-induced nephrotoxicity in adult mice.

    Science.gov (United States)

    Ben Saad, Hajer; Gargouri, Manel; Kallel, Fatma; Chaabene, Rim; Boudawara, Tahia; Jamoussi, Kamel; Magné, Christian; Mounir Zeghal, Khaled; Hakim, Ahmed; Ben Amara, Ibtissem

    2017-05-01

    Potassium bromate (KBrO3 ), an environmental pollutant, is a well-known human carcinogen and a potent nephrotoxic agent. Currently, natural products have built a well-recognized role in the management of many diseases induced by pollutants. As potent natural sources of bioactive compounds, marine algae have been demonstrated to be rich in novel secondary metabolites with a broad range of biological functions. In this study, adults male mice were orally treated for 15 days with KBrO3 (0.5 g/L) associated or not with extract of Alsidium corallinum, a red Mediterranean alga. In vitro study demonstrated that algal extract has antioxidant efficacy attributable to the presence of flavonoids and polyphenols. Among these, Liquid chromatography-mass spectrometry analysis showed A. corallinum is rich in kaempferol, apigenin, catechin, and quercetin flavonoids. In vivo study showed that supplementation with the alga significantly prevented KBrO3 -induced nephrotoxicity as indicated by plasma biomarkers (urea, uric acid, and creatinin levels) and oxidative stress related parameters (malondialdehyde, superoxide dismutase, catalase, glutathione peroxidase, reduced glutathione, vitamin C, hydrogen peroxide, protein oxidation products) in kidney tissue. The corrective effect of A. corallinum on KBrO3 -induced kidney injury was also supported by molecular and histopathological observations. In conclusion, it was established that the red alga, thanks to its bioactive compounds, effectively counteracts toxic effects of KBrO3 and could be a useful coadjuvant agent for treatment of this pollutant poisonings. © 2016 Wiley Periodicals, Inc. Environ Toxicol 32: 1475-1486, 2017. © 2016 Wiley Periodicals, Inc.

  14. Sensitive Spectrophotometric Methods for the Determination of Gatifloxacin in Pharmaceuticals Using Bromate-Bromide, Methylene Blue and Rhodamine-B as Reagents

    Directory of Open Access Journals (Sweden)

    K. Basavaiah

    2007-01-01

    Full Text Available Two new simple, precise, rapid and extraction-free spectrophotometric methods are proposed for the determination of gatifloxacin(GTF using bromate-bromide mixture and two dyes, methylene blue and rhodamine B, as reagents. Spectrophotometric methods entail the addition of a known excess of bromate-bromide mixture to GTF in hydrochloric acid medium followed by determination of residual bromine by reacting with a fixed amount of either methylene blue and measuring the absorbance at 665 nm (Method A or rhodamine B and measuring the absorbance at 555 nm (Method B. Beer᾽s law is obeyed in the ranges, 0.5-5.0 and 0.2-1.5 μg mL-1 for method A and method B, respectively. The apparent molar absorptivities are calculated to be 5.6×104 and 9.6×104 L mol-1cm-1 for method A and method B, respectively, and the corresponding Sandell sensitivity values are 0.0071 and 0.0042 μg cm-2. The methods were successfully applied to the assay of GTF in pharmaceutical formulations with satisfactory results.

  15. Effects of vanillin on potassium bromate-induced neurotoxicity in adult mice: impact on behavior, oxidative stress, genes expression, inflammation and fatty acid composition.

    Science.gov (United States)

    Ben Saad, Hajer; Kharrat, Nadia; Driss, Dorra; Gargouri, Manel; Marrakchi, Rim; Jammoussi, Kamel; Magné, Christian; Boudawara, Tahia; Ellouz Chaabouni, Samia; Zeghal, Khaled Mounir; Hakim, Ahmed; Ben Amara, Ibtissem

    2017-07-01

    Vanillin is known to possess important antioxidant activity. The current study was conducted to establish the therapeutic efficiency of vanillin against potassium bromate (KBrO3)-induced depression-like behavior and oxidative stress in mice. Mice were exposed during 15 days either to potassium bromate (KBrO3), KBrO3+ vanillin or to only vanillin. Our results revealed a significant modification in the fatty acid composition of the KBrO3-treated mice. In addition, KBrO3 induced a significant reduction in enzymatic activities and gene expressions, Na(+) -K(+ ) and Mg(2+)-ATPases, acetylcholinesterase and butylcholinesterase activities. The gene expression of tumor necrosis factor-α, interleukin-1β, interleukin-6 and COX2, significantly increased in the cerebrum of KBrO3-treated group. Histopathological observations were consistent with these effects. Co-treatment with vanillin significantly attenuated KBrO3-induced oxidative stress and inflammation. This work suggests that vanillin mitigates KBrO3-induced depression, and that this neuroprotective effect proceeds through anti-oxidant and anti-inflammatory activities.

  16. Complex dynamics in the bromate/hypophosphite/acetone/manganese and ferroin system; Dinamica complexa no sistema bromato/hipofosfito/acetona/manganes e ferroina

    Energy Technology Data Exchange (ETDEWEB)

    Tokoro, Gustavo; Oliveira, Hyrla C.L.; Varela, Hamilton [Universidade de Sao Paulo (USP), Sao Carlos, SP (Brazil). Inst. de Quimica]. E-mail: varela@iqsc.usp.br

    2007-07-01

    New chemical systems have been recently designed for the study of complex phenomena such as oscillatory dynamics in the temporal domain and spatio-temporal pattern formation. Systems derived from oscillators based on the chemistry of bromate are the most extensively studied, with the celebrated Belousov-Zhabotinsky (BZ) reaction being the most popular example. Problems such as the formation of bubbles (CO{sub 2}) and solid precipitate in the course of the reaction and the occurrence of simply short-lived oscillations under batch conditions are very common and, in some cases, compromise the use of some of these systems. It is investigated in this paper the dynamic behavior of the bromate/hypophosphite/acetone/dual catalyst system, which has been suggested as an interesting alternative to circumvent those inconvenient. In this work, manganese and ferroin are employed as catalysts and the complete system (BrO{sub 3}-/H{sub 2}PO{sub 2} -/acetone/Mn(II)-ferroin) is studied under batch conditions. Temporal symmetry breaking was studied in a reactor under agitation by means of simultaneous records of the potential changes of platinum and Ag/AgBr electrodes, both measured versus a reversible hydrogen electrode. Additionally, spatio-temporal formation of target patterns and spiral waves were obtained when the oscillating mixture was placed in a quasi two-dimensional reactor. (author)

  17. Protective effect of taurine against potassium bromate-induced hemoglobin oxidation, oxidative stress, and impairment of antioxidant defense system in blood.

    Science.gov (United States)

    Ahmad, Mir Kaisar; Mahmood, Riaz

    2016-03-01

    Potassium bromate (KBrO3 ) is widely used as a food-additive and is a major water disinfection by-product. KBrO3 causes severe toxicity in humans and experimental animals. Bromate is considered a probable human carcinogen and a complete carcinogen in animals. We have investigated the potential role of taurine in protecting against KBrO3 -induced oxidative stress in rat blood. Animals were given taurine for 5 days prior to KBrO3 and then sacrificed. Blood was collected and used to prepare hemolysates and plasma, which were then used for the analysis of several biochemical parameters. Administration of single oral dose of KBrO3 alone induced hepato- and nephro-toxicity as evident by elevated marker levels in plasma. Lipid peroxidation and protein oxidation were increased both in plasma and erythrocytes, suggesting the induction of oxidative stress. KBrO3 increased methemoglobin, nitric oxide, and hydrogen peroxide levels. It also altered the activities of the major antioxidant enzymes and lowered the antioxidant power of blood. Administration of taurine, prior to treatment with KBrO3 , resulted in significant attenuation in all these parameters but the administration of taurine alone had no effect. These results show that taurine is effective in mitigating the oxidative insult induced in rat blood by KBrO3 . © 2014 Wiley Periodicals, Inc.

  18. Chemoprotective effect of taurine on potassium bromate-induced DNA damage, DNA-protein cross-linking and oxidative stress in rat intestine.

    Directory of Open Access Journals (Sweden)

    Mir Kaisar Ahmad

    Full Text Available Potassium bromate (KBrO3 is widely used as a food additive and is a major water disinfection by-product. It induces multiple organ toxicity in humans and experimental animals and is a probable human carcinogen. The present study reports the protective effect of dietary antioxidant taurine on KBrO3-induced damage to the rat intestine. Animals were randomly divided into four groups: control, KBrO3 alone, taurine alone and taurine+ KBrO3. Administration of KBrO3 alone led to decrease in the activities of intestinal brush border membrane enzymes while those of antioxidant defence and carbohydrate metabolism were also severely altered. There was increase in DNA damage and DNA-protein cross-linking. Treatment with taurine, prior to administration of KBrO3, resulted in significant attenuation in all these parameters but the administration of taurine alone had no effect. Histological studies supported these biochemical results showing extensive intestinal damage in KBrO3-treated animals and greatly reduced tissue injury in the taurine+ KBrO3 group. These results show that taurine ameliorates bromate induced tissue toxicity and oxidative damage by improving the antioxidant defence, tissue integrity and energy metabolism. Taurine can, therefore, be potentially used as a therapeutic/protective agent against toxicity of KBrO3 and related compounds.

  19. Chemoprotective effect of taurine on potassium bromate-induced DNA damage, DNA-protein cross-linking and oxidative stress in rat intestine.

    Science.gov (United States)

    Ahmad, Mir Kaisar; Khan, Aijaz Ahmed; Ali, Shaikh Nisar; Mahmood, Riaz

    2015-01-01

    Potassium bromate (KBrO3) is widely used as a food additive and is a major water disinfection by-product. It induces multiple organ toxicity in humans and experimental animals and is a probable human carcinogen. The present study reports the protective effect of dietary antioxidant taurine on KBrO3-induced damage to the rat intestine. Animals were randomly divided into four groups: control, KBrO3 alone, taurine alone and taurine+ KBrO3. Administration of KBrO3 alone led to decrease in the activities of intestinal brush border membrane enzymes while those of antioxidant defence and carbohydrate metabolism were also severely altered. There was increase in DNA damage and DNA-protein cross-linking. Treatment with taurine, prior to administration of KBrO3, resulted in significant attenuation in all these parameters but the administration of taurine alone had no effect. Histological studies supported these biochemical results showing extensive intestinal damage in KBrO3-treated animals and greatly reduced tissue injury in the taurine+ KBrO3 group. These results show that taurine ameliorates bromate induced tissue toxicity and oxidative damage by improving the antioxidant defence, tissue integrity and energy metabolism. Taurine can, therefore, be potentially used as a therapeutic/protective agent against toxicity of KBrO3 and related compounds.

  20. Sensitive and rapid titrimetric and spectrophotometric methods for the determination of stavudine in pharmaceuticals using bromate-bromide and three dyes

    Directory of Open Access Journals (Sweden)

    Kanakapura Basavaiah

    2008-06-01

    Full Text Available Four sensitive and rapid methods for the determination of stavudine (STV in bulk drug and in dosage forms were developed and optimized. In titrimetry, aqueous solution of STV was treated with a known excess of bromate-bromide in HCl medium followed by estimation of unreacted bromine by iodometric back titration. Spectrophotometric methods involve the addition of a measured excess of bromate-bromide in HCl medium and subsequent estimation of the residual bromine by reacting with a fixed amount of methyl orange, indigocarmine or thymol blue followed by measurement of absorbance at 520 nm (method A, 610 nm (method B or 550 nm (method C. In all the methods, the amount of bromate reacted corresponds to the amount of STV. Calculations in titrimetry were based on a 1:0.666 (STV:KBrO3 stoichiometry and the method was found to be applicable over 3.5-10 mg range. A linear increase in absorbance with concentration of STV was observed in the spectrophotometric methods, and the Beer's law was obeyed over the concentration ranges 0.125-1.75, 1-10 and 1-9.0 µg mL-1 STV for method A, method B and method C, respectively. The methods when applied to the determination of STV in tablets and capsules were found to give satisfactory results.Este trabalho descreve quatro métodos rápidos e sensíveispara a determinação de estavudina (STV na matéria-prima ou em produtos formulados. Soluções aquosas de STV podem ser tituladas tratando-as com excesso de bromato-brometo em meio ácido clorídrico, seguido da determinação iodimétrica de bromo em excesso. Métodos espectrofotométricos tambémenvolvem a adição de excesso de bromato-brometo à amostra, seguida da determinação de bromo residual por adição de uma quantidade fixa de alaranjado de metila, índigo-carmim ou azul de timol, e de medidas de absorbância nos comprimentos de onda apropriados: 520, 610 ou 550 nm. Em todos os métodos, a quantidade de bromato consumida corresponde à quantidade de STV e

  1. Oscillatory reactions in the acetone-glucose-sodium bromate-sulfuric acid system with a tetraazamacrocyclic copper (II complex as a catalyst

    Directory of Open Access Journals (Sweden)

    Hu Lin

    2016-01-01

    Full Text Available The behavior of glycolysis concerning the biochemical reaction was thought to be similar to the oscillatory reaction with glucose being the substrate. The objective of this research is to find a new oscillatory system and study its relevant properties, so new Cu (II-catalyzed oscillating reaction involved glucose and acetone as the double substrates was investigated systematically. As a function of reaction temperature and concentration of glucose, bromate, and acetone, the features in this novel oscillation system was studied. The results showed that the activation energy reached up to 90.839 KJ/mol and the oxidized product of the double substrates provided the impetus in the course of the new oscillating reaction. A tentative mechanism was considered on the basis of FNK.

  2. Dose-response analysis of bromate-induced DNA damage and mutagenicity is consistent with low-dose linear, nonthreshold processes.

    Science.gov (United States)

    Spassova, Maria A; Miller, David J; Eastmond, David A; Nikolova, Nadejda S; Vulimiri, Suryanarayana V; Caldwell, Jane; Chen, Chao; White, Paul D

    2013-01-01

    Mutagenic agents have long been inferred to act through low-dose linear, nonthreshold processes. However, there is debate about this assumption, with various studies interpreting datasets as showing thresholds for DNA damage and mutation. We have applied rigorous statistical analyses to investigate the shape of dose-response relationships for a series of in vitro and in vivo genotoxicity studies using potassium bromate (KBrO(3) ), a water ozonation byproduct that is bioactivated to a reactive species causing oxidative damage to DNA. We analyzed studies of KBrO(3) genotoxicity where no-effect/threshold levels were reported as well as other representative datasets. In all cases, the data were consistent with low-dose linear models. In the majority of cases, the data were fit either by a linear (straight line) model or a model which was linear at low doses and showed a saturation-like downward curvature at high doses. Other datasets with apparent upward curvature were still adequately represented by models that were linear at low dose. Sensitivity analysis of datasets showing upward curvature revealed that both low-dose linear and nonlinear models provide adequate fits. Additionally, a simple biochemical model of selected key processes in bromate-induced DNA damage was developed and illustrated a situation where response for early primary events suggested an apparent threshold while downstream events were linear. Overall, the statistical analyses of DNA damage and mutations induced by KBrO(3) are consistent with a low-dose linear response and do not provide convincing evidence for the presence of a threshold. Copyright © 2012 Wiley Periodicals, Inc.

  3. New Sensitive Spectrophotometric Methods for the Determination of Raloxifene Hydrochloride in Pharmaceuticals Using Bromate-Bromide,Methyl Orange and Indigo Carmine

    Directory of Open Access Journals (Sweden)

    K Basavaiah

    2006-01-01

    Full Text Available Two new sensitive spectrophotometric methods are proposed for the determination of raloxifene hydrochloride (RLX using bromate-bromide mixture and two dyes, methyl orange and indigocarmine, as reagents. The methods entail the addition of a known excess of bromate-bromide mixture to RLX in hydrochloric acid medium followed by determination of residual bromine by reacting with a fixed amount of either methyl orange and measuring the absorbance at 520 nm (Method A or indigo carmine and measuring the absorbance at 610 nm (Method B. In both methods, the amount of bromine reacted corresponds to the amount of RLX. The absorbance is found to increase linearly with concentration of RLX. Under the optimum conditions, RLX could be assayed in the concentration range 0.1-2.0 and 0.5-6.0 μg mL-1 by method A and method B, respectively. The apparent molar absorptivities are calculated to be 1.9×105 and 4.5×104 L mol-1cm-1 for method A and method B, respectively, and the corresponding Sandell sensitivity values are 0.003 and 0.011 μg cm-2. The limits of detection and quantification are also reported for both methods. Intra-day and inter-day precision and accuracy of the developed methods were evaluated as per the current ICH guidelines. The methods were successfully applied to the assay of RLX in its tablet formulation and the results were compared with those of a reference method by calculating the Student’s t-value and F-value. No interference was observed from common tablet adjuvants. The accuracy and reliability of the methods were further ascertained by recovery experiments via standard-addition procedure.

  4. Electrocatalytic reduction of bromate ion using a polyaniline-modified electrode: An efficient and green technology for the removal of BrO{sub 3}{sup -} in aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Ding Liang; Li Qin; Cui Hao; Tang Rong; Xu Hui; Xie Xianchuan [State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, 22 Hankou Road, Nanjing 210093 (China); Zhai Jianping, E-mail: jpzhai@nju.edu.c [State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, 22 Hankou Road, Nanjing 210093 (China)

    2010-12-01

    The electrocatalytic reduction of bromate ion (BrO{sub 3}{sup -}) was investigated in a three-electrode system using polyaniline (PANI) as the electrode material. Bromate ion reduction and Br{sup -} removal were observed during electrochemical treatment because of the catalytic and doping capabilities of the PANI film. BrO{sub 3}{sup -} removal efficiency in the 0.10 mol L{sup -1} Na{sub 2}SO{sub 4} supporting electrolyte achieved 99% at pH 7 in 25 min, with no bromide ion detected in the solution. Optimal removal was found in pH range 6-7, and the pH of the solution had a significant impact on bromate reduction. A reduction mechanism was also discussed by analyzing the cyclic voltammograms of the reduction process and X-ray photoelectron spectra of the main elements (N 1s and Br 3d) on the PANI surface. We propose that during the electrocatalytic reduction process, bromate is reduced to bromide because of the loss of electrons from the nitrogen atoms on the PANI chains. The doping of the resultant Br{sup -} ions in the PANI film has an important role in avoiding further oxidation of Br{sup -} to BrO{sub 3}{sup -}. The used PANI film can be regenerated by de-doping the Br{sup -} ions with a 0.5 mol L{sup -1} H{sub 2}SO{sub 4} solution. Thus the process can be considered efficient and green.

  5. Use of weak ion association in the separation of inorganic anions by capillary electrophoresis with specific application to simultaneous-trace determination of bromate and iodate in drinking water

    Directory of Open Access Journals (Sweden)

    Julius Mbuna

    2008-04-01

    Full Text Available In this work weak ion association was used to effect selectivity and detection of inorganic anions with environmental or health significance by capillary electropheresis, CE. Tetrabutylammonium ion was used as a pairing anion to separate mixtures containing closely or co-migrating inorganic anions at pHs 3.8 and pH 7. Despite taking a longer analysis time, better resolution is achieved at pH 7 than 3.8. Trace level of bromate and iodate present in drinking water were determined after online pre-concentration by field enhanced sample injection (FESI technique. Consequently an internal standard (SCN- was employed, which entailed the use of tetrabutylammonium ion as a pairing cation to resolve the internal standard from a co-migrating broad peak. The LODs (S/N = 3 were 7.8 x 10-10 M (10 ppb and 1.2 x 10-9 M (0.21 ppb for bromate and iodate, respectively. The method was subsequently used to determine bromate and iodate levels in drinking water.

  6. Combination of UV absorbance and electron donating capacity to assess degradation of micropollutants and formation of bromate during ozonation of wastewater effluents.

    Science.gov (United States)

    Chon, Kangmin; Salhi, Elisabeth; von Gunten, Urs

    2015-09-15

    In this study, the changes in UV absorbance at 254 nm (UVA254) and electron donating capacity (EDC) were investigated as surrogate indicators for assessing removal of micropollutants and bromate formation during ozonation of wastewater effluents. To measure the EDC, a novel method based on size exclusion chromatography followed by a post-column reaction was developed and calibrated against an existing electrochemical method. Low specific ozone doses led to a more efficient abatement of EDC than of UVA254. This was attributed to the abatement of phenolic moieties in the dissolved organic matter (DOM), which lose their EDC upon oxidation, but are partially transformed into quinones, which still absorb in the measured UV range. For higher specific ozone doses, the relative EDC abatement was lower than the relative UVA abatement, which can be explained by the oxidation of UV absorbing moieties (e.g. non-activated aromatic compounds), which contribute less to EDC. The abatement of the selected micropollutants (i.e., 17α-ethinylestradiol (EE2), carbamazepine (CBZ), atenolol (ATE), bezafibrate (BZF), ibuprofen (IBU), and p-chlorobenzoic acid (pCBA)) varied significantly depending on their reactivity with ozone in the examined specific ozone dose range of 0-1.45 mgO3/mgDOC. The decrease of EE2 and CBZ with high ozone reactivity was linearly proportional to the reduction of the relative residuals of UVA254 and EDC. The abatement of ATE, BZF, IBU, and pCBA with intermediate to low ozone reactivities was not significant in a first phase (UVA254/UVA254,0 = 1.00-0.70; EDC/EDC0 = 1.00-0.56) while their abatement was more efficient than the degradation of the relative residual UVA254 and much more noticeable than the degradation of the relative residual EDC in a second phase (UVA254/UVA254,0 = 0.70-0.25; EDC/EDC0 = 0.56-0.25) because the partially destroyed UV absorbing and electron donating DOM moieties become recalcitrant to ozone attack. Bromate formation was

  7. Oxyhalogen-sulfur chemistry: kinetics and mechanism of oxidation of chemoprotectant, sodium 2-mercaptoethanesulfonate, MESNA, by acidic bromate and aqueous bromine.

    Science.gov (United States)

    Adigun, Risikat Ajibola; Mhike, Morgen; Mbiya, Wilbes; Jonnalagadda, Sreekanth B; Simoyi, Reuben H

    2014-03-27

    The oxidation of a well-known chemoprotectant in anticancer therapies, sodium 2-mercaptoethanesulfonate, MESNA, by acidic bromate and aqueous bromine was studied in acidic medium. Stoichiometry of the reaction is: BrO3(-) + HSCH2CH2SO3H → Br(-) + HO3SCH2CH2SO3H. In excess bromate conditions the stoichiometry was deduced to be: 6BrO3(-) + 5HSCH2CH2SO3H + 6H(+) → 3Br2 + 5HO3SCH2CH2SO3H + 3H2O. The direct reaction of bromine and MESNA gave a stoichiometric ratio of 3:1: 3Br2 + HSCH2CH2SO3H + 3H2O → HO3SCH2CH2SO3H + 6Br(-) + 6H(+). This direct reaction is very fast; within limits of the mixing time of the stopped-flow spectrophotometer and with a bimolecular rate constant of 1.95 ± 0.05 × 10(4) M(-1) s(-1). Despite the strong oxidizing agents utilized, there is no cleavage of the C-S bond and no sulfate production was detected. The ESI-MS data show that the reaction proceeds via a predominantly nonradical pathway of three consecutive 2-electron transfers on the sulfur center to obtain the product 1,2-ethanedisulfonic acid, a well-known medium for the delivery of psychotic drugs. Thiyl radicals were detected but the absence of autocatalytic kinetics indicated that the radical pathway was a minor oxidation route. ESI-MS data showed that the S-oxide, contrary to known behavior of organosulfur compounds, is much more stable than the sulfinic acid. In conditions where the oxidizing equivalents are limited to a 4-electron transfer to only the sulfinic acid, the products obtained are a mixture of the S-oxide and the sulfonic acid with negligible amounts of the sulfinic acid. It appears the S-oxide is the preferred conformation over the sulfenic acid since no sulfenic acids have ever been stabilized without bulky substituent groups. The overall reaction scheme could be described and modeled by a minimal network of 18 reactions in which the major oxidants are HOBr and Br2(aq).

  8. Understanding mechanisms of pressure-assisted electrokinetic injection: application to analysis of bromate, arsenic and selenium species in drinking water by capillary electrophoresis-mass spectrometry.

    Science.gov (United States)

    Zhang, Huijuan; Gavina, Jennilee; Feng, Yong-Lai

    2011-05-20

    The mechanism underlying the enrichment power by pressure-assisted electrokinetic injection (PAEKI) in capillary electrophoresis (CE) was investigated for on-line pre-concentration of arsenic [As(III) and As(V)], selenium [Se(IV) and Se(VI)] and bromate (BrO(3)(-)). Analyte diffusion behaviour from PAEKI sample plugs were evaluated by monitoring peak broadening as a function of stagnant time and position in the capillary. During PAEKI, anionic analytes accumulate at the sample-separation buffer boundary. We proposed that a counter-ion layer formed in PAEKI, where a cation layer was formed at the separation buffer side of boundary. The cation layer served as a soft boundary which impeded zone broadening via electrostatic attraction between layers. This effect likely played an important role in maintaining focused analyte bands by suppressing diffusion. Comparison of analyte behaviour in PAEKI injected sample plugs to behaviour in hydrodynamically injected ones proved the existence of a counter-ion layer. The dependence of analyte diffusion in PAEKI plugs on electrochemical properties (viscosity, conductivity, electrophoretic mobility) further supported the hypothesis. Additionally, it was noted that analytes with low electrophoretic mobility were more efficiently pre-concentrated by PAEKI and were less subject to forces of dispersion than analytes with greater electrophoretic mobility. PAEKI-CE coupled to electrospray tandem mass spectroscopy (ESI-MS/MS) was then optimized and validated for detection of arsenic, selenium and bromate in water samples. On-line enrichment of the target analytes was achieved with 1-3 ng mL(-1) detection limits, which was below the maximum contaminant levels in drinking water for all five anions studied. Noteworthy, the potential of the method for unbiased detection of molecular species in untreated water was demonstrated. No contamination was detected in the water samples tested; however, recovery was 90-118% for spiked samples. The

  9. Influence of UV lamp, sulfur(IV) concentration, and pH on bromate degradation in UV/sulfite systems: Mechanisms and applications.

    Science.gov (United States)

    Xiao, Qian; Wang, Ting; Yu, Shuili; Yi, Peng; Li, Lei

    2017-03-15

    Bromate (BrO3(-)) is a possible human carcinogen regulated worldwide at a strict standard of 10 μg/L in drinking water. Removal of BrO3(-) by advanced reduction processes (ARPs) has attracted much attention due to its high reduction efficiency and easier combination with ultraviolet (UV) disinfection. In this study, we employed a UV/sulfite process to degrade BrO3(-) and studied the effects of UV lamp, sulfur(IV) concentration, and pH on effectiveness of the system in degrading BrO3(-). Low-pressure UV lamps (UV-L) instead of medium-pressure UV lamps (UV-M) were selected because of the high ultraviolet-C (UV-C) efficiency of UV-L. The increased sulfur(IV) concentration is proportionally correlated with enhanced degradation kinetics. BrO3(-) reduction was improved by increasing pH when pH is within 6.0-9.0, and principal component analysis demonstrated that pH is the most influential factor over sulfur(IV) concentration and type of UV lamp. Degradation mechanisms at different pH levels were subsequently investigated. Results showed that the reduction reactions are induced by hydrated electron (eaq(-)) at pH > 9.0, by H at pH 4.0, and by both eaq(-) and H at pH 7.0. Effective quantum efficiency for the formation of eaq(-) and H in the photocatalytic systems was determined to be 0.109 ± 0.001 and 0.034 ± 0.001 mol E(-1), respectively. Furthermore, mass balance calculation of bromine and sulfur at pH 7 showed that bromide, sulfate and possibly dithionate ions were the major products, and a degradation pathway was proposed accordingly. Moreover, UV/sulfite processes could reduce the initial bromate concentration of 0.1 mM by 82% and 95% in the presence and absence of O2 in tap water respectively, and 99% in the absence of O2 in deionized water within 20 min at pH 9.0 and 2.0 mM sulfur (IV). Copyright © 2017 Elsevier Ltd. All rights reserved.

  10. Multiple linear regression model for bromate formation based on the survey data of source waters from geographically different regions across China.

    Science.gov (United States)

    Yu, Jianwei; Liu, Juan; An, Wei; Wang, Yongjing; Zhang, Junzhi; Wei, Wei; Su, Ming; Yang, Min

    2015-01-01

    A total of 86 source water samples from 38 cities across major watersheds of China were collected for a bromide (Br(-)) survey, and the bromate (BrO3 (-)) formation potentials (BFPs) of 41 samples with Br(-) concentration >20 μg L(-1) were evaluated using a batch ozonation reactor. Statistical analyses indicated that higher alkalinity, hardness, and pH of water samples could lead to higher BFPs, with alkalinity as the most important factor. Based on the survey data, a multiple linear regression (MLR) model including three parameters (alkalinity, ozone dose, and total organic carbon (TOC)) was established with a relatively good prediction performance (model selection criterion = 2.01, R (2) = 0.724), using logarithmic transformation of the variables. Furthermore, a contour plot was used to interpret the influence of alkalinity and TOC on BrO3 (-) formation with prediction accuracy as high as 71 %, suggesting that these two parameters, apart from ozone dosage, were the most important ones affecting the BFPs of source waters with Br(-) concentration >20 μg L(-1). The model could be a useful tool for the prediction of the BFPs of source water.

  11. Altered hepatic mRNA expression of immune response-associated DNA damage in mice liver induced by potassium bromate: Protective role of vanillin.

    Science.gov (United States)

    Ben Saad, Hajer; Driss, Dorra; Ben Amara, Ibtissem; Boudawara, Ons; Boudawara, Tahia; Ellouz Chaabouni, Samia; Mounir Zeghal, Khaled; Hakim, Ahmed

    2016-12-01

    Chronic exposure to potassium bromate (KBrO3 ), a toxic halogen existing widely in the environment, environment through contaminated drinking water, has become a global problem of public health. The present study investigates the protective role of vanillin against KBrO3 induced oxidative stress, distruption in inflammatory cytokines expression, DNA damage, and histopathological changes. Adult mice were exposed orally to KBrO3 (2g/L of drinking water) for 2 weeks The co-administration of vanillin to the KBrO3 -treated mice significantly prevented the plasma transaminases increase in. Furthermore, it inhibited hepatic lipid peroxidation (malondialdehyde), advanced oxidation protein product (AOPP) and protein carbonyl (PCO) formation and attenuated the KBrO3 -mediated depletion of enzymatic and non enzymatic antioxidants catalase, superoxide dismutase, and glutathione peroxidase activities and glutathione level in the liver. In addition, vanillin markedly attenuated the expression levels of proinflammatory cytokines, including tumor necrosis factor-α, interleukin-1β, interleukin-6, and COX2 and prevented KBrO3 -induced hepatic cell alteration and necrosis, as indicated by histopathological data. DNA damage, as assessed by the alkaline comet assay, was also found to be low in the co-treated group. Thus, these findings show that vanillin acts as potent chemopreventive agent against KBrO3 -mediated liver oxidative stress and genotoxicity through its antioxidant properties. © 2015 Wiley Periodicals, Inc. Environ Toxicol 31: 1796-1807, 2016. © 2015 Wiley Periodicals, Inc.

  12. Evaluation of repeated dose micronucleus assays of the liver and gastrointestinal tract using potassium bromate: a report of the collaborative study by CSGMT/JEMS.MMS.

    Science.gov (United States)

    Okada, Emiko; Fujiishi, Yohei; Narumi, Kazunori; Kado, Shoichi; Wako, Yumi; Kawasako, Kazufumi; Kaneko, Kimiyuki; Ohyama, Wakako

    2015-03-01

    The food additive potassium bromate (KBrO3) is known as a renal carcinogen and causes chromosomal aberrations in vitro without metabolic activation and in vivo in hematopoietic and renal cells. As a part of a collaborative study by the Mammalian Mutagenicity Study group, which is a subgroup of the Japanese Environmental Mutagen Society, we administered KBrO3 to rats orally for 4, 14, and 28 days and examined the micronucleated (MNed) cell frequency in the liver, glandular stomach, colon, and bone marrow to confirm whether the genotoxic carcinogen targeting other than liver and gastrointestinal (GI) tract was detected by the repeated dose liver and GI tract micronucleus (MN) assays. In our study, animals treated with KBrO3 showed some signs of toxicity in the kidney and/or stomach. KBrO3 did not increase the frequency of MNed cells in the liver and colon in any of the repeated dose studies. However, KBrO3 increased the frequency of MNed cells in the glandular stomach and bone marrow. Additionally, the MNed cell frequency in the glandular stomach was not significantly affected by the difference in the length of the administration period. These results suggest that performing the MN assay using the glandular stomach, which is the first tissue to contact agents after oral ingestion, is useful for evaluating the genotoxic potential of chemicals and that the glandular stomach MN assay could be integrated into general toxicity studies. Copyright © 2014 Elsevier B.V. All rights reserved.

  13. Study on the interaction among pyronine Y, potassium bromate and naphthols by absorption, three-dimension fluorescence and resonance light scattering spectra and their application

    Science.gov (United States)

    Yang, Hongmei; Wang, Yongsheng; Wang, Ying; Li, Junhong; Xiao, Xilin; Tan, Xuan

    2008-12-01

    A novel method for the determination of trace naphthols was proposed based on naphthols, potassium bromate and pyronine Y in dilute sulfuric acid medium can react to form ion-association complexes, which not only resulted in the changes of the three-dimension fluorescence spectra, absorption spectra and the quenching of fluorescence, but also resulted in the great enhancement of resonance light scattering (RLS). The characteristics of RLS spectra, the effective factors and optimum conditions of reaction were studied. It was found that the enhanced intensity of RLS at 396 nm was proportional to the concentration of 1-naphthol and 2-naphthol in the range of 41.4 ˜ 3024 ng mL -1 and 38.3 ˜ 3068 ng mL -1, respectively. The urine samples analysis of the relative standard deviation was 3.1-7.1% and the average recovery was 96.0% ( n = 6). The present method had been applied to the determination of trace naphthols in human urine, the obtained results were in good agreement with those obtained by the HPLC method; moreover, we had carried on an initial study of the reaction mechanism in terms of spectral characteristics.

  14. New inorganic (an)ion exchangers with a higher affinity for arsenate and a competitive removal capacity towards fluoride, bromate, bromide, selenate, selenite, arsenite and borate

    KAUST Repository

    Chubar, Natalia

    2011-12-01

    Highly selective materials and effective technologies are needed to meet the increasingly stronger drinking water standards for targeted ionic species. Inorganic ion exchangers based on individual and mixed-metal hydrous oxides (or mixed adsorbents that contain inorganic ion exchangers in their composition) are adsorptive materials that are capable of lowering the concentrations of anionic contaminants, such as H 2AsO 4 -, H 3AsO 3, F -, Br -, BrO 3 -, HSeO 4 -, HSeO 3 - and H 3BO 3, to 10 μg/L or less. To achieve a higher selectivity towards arsenate, a new ion exchanger based on Mg-Al hydrous oxides was developed by a novel, cost-effective and environmentally friendly synthesis method via a non-traditional (alkoxide-free) sol-gel approach. The exceptional adsorptive capacity of the Mg-Al hydrous oxides towards H 2AsO 4 - (up to 200 mg[As]/gdw) is due to the high affinity of this sorbent towards arsenate (steep equilibrium isotherms) and its fast adsorption kinetics. Because of the mesoporous (as determined by N 2 adsorption and SEM) and layered (as determined by XRD and FTIR) structure of the ion-exchange material as well as the abundance of anion exchange sites (as determined by XPS and potentiometric titration) on its surface the material demonstrated very competitive (or very high) removal capacity towards other targeted anions, including fluoride, bromide, bromate, selenate, selenite, and borate. © 2011 IWA Publishing.

  15. Formation of bromate and halogenated disinfection byproducts during chlorination of bromide-containing waters in the presence of dissolved organic matter and CuO

    KAUST Repository

    Liu, Chao

    2015-12-02

    Previous studies showed that significant bromate (BrO3-) can be formed via the CuO-catalyzed disproportionation of hypobromous acid (HOBr) pathway. In this study, the influence of CuO on the formation of BrO3- and halogenated disinfection byproducts (DBPs) (e.g., trihalomethanes, THMs and haloacetic acids, HAAs) during chlorination of six dissolved organic matter (DOM) isolates was investigated. Only in the presence of slow reacting DOM (from treated Colorado River water, i.e., CRW-BF-HPO), significant BrO3- formation is observed, which competes with bromination of DOM (i.e., THM and HAA formation). Reactions between HOBr and 12 model compounds in the presence of CuO indicates that CuO-catalyzed HOBr disproportionation is completely inhibited by fast reacting phenols, while it predominates in the presence of practically unreactive compounds (acetone, butanol, propionic, and butyric acids). In the presence of slow reacting di- and tri-carboxylic acids (oxalic, malonic, succinic, and citric acids), BrO3- formation varies, depending on its competition with bromoform and dibromoacetic acid formation (i.e., bromination pathway). The latter pathway can be enhanced by CuO due to the activation of HOBr. Therefore, increasing CuO dose (0-0.2 g L-1) in a reaction system containing chlorine, bromide, and CRW-BF-HPO enhances the formation of BrO3-, total THMs and HAAs. Factors including pH and initial reactant concentrations influence the DBP formation. These novel findings have implications for elevated DBP formation during transportation of chlorinated waters in copper-containing distribution systems.

  16. Photo-reduction of bromate in drinking water by metallic Ag and reduced graphene oxide (RGO) jointly modified BiVO4 under visible light irradiation.

    Science.gov (United States)

    Chen, Fei; Yang, Qi; Zhong, Yu; An, Hongxue; Zhao, Jianwei; Xie, Ting; Xu, Qiuxiang; Li, Xiaoming; Wang, Dongbo; Zeng, Guangming

    2016-09-15

    Bromate (BrO3(-)), an oxyhalide disinfection by-product (DBP) in drinking water, has been demonstrated to be carcinogenic and genotoxic. In the current work, metallic Ag and reduced graphene oxide (RGO) co-modified BiVO4 was successfully synthesized by a stepwise chemical method coupling with a photo-deposition process and applied in the photo-reduction of BrO3(-) under visible light irradiation. In this composite, metallic Ag acted as an electron donor or mediator and RGO enhanced the BrO3(-) adsorption onto the surface of catalysts as well as an electron acceptor to restrict the recombination of photo-generated electron-hole pairs. The Ag@BiVO4@RGO composite exhibited greater photo-reduction BrO3(-) performance than pure BiVO4, Ag@BiVO4 and RGO@BiVO4 under identical experimental conditions: initial BrO3(-) concentration 150 μg/L, catalyst dosage 0.5 g/L, pH 7.0 and visible light (λ > 420 nm). The photoluminescence spectra (PL), electron-spin resonance (ESR), photocurrent density (PC) and electrochemical impedance spectroscopy (EIS) measurements indicated that the modified BiVO4 enhanced the photo-generated electrons and separated the electron-hole pairs. The photocatalytic reduction efficiency for BrO3(-) removal decreased with the addition of electron quencher K2S2O8, suggesting that electrons were the primary factor in this photo-reduction process. The declining photo-reduction efficiency of BrO3(-) in tap water should attribute to the consumption of photo-generated electrons by coexisting anions and the adsorption of dissolved organic matter (DOM) on graphene surface. The overall results indicate a promising application potential for photo-reduction in the DBPs removal from drinking water. Copyright © 2016 Elsevier Ltd. All rights reserved.

  17. Effective removal of bromate in nitrate-reducing anoxic zones during managed aquifer recharge for drinking water treatment: Laboratory-scale simulations.

    Science.gov (United States)

    Wang, Feifei; van Halem, Doris; Ding, Lei; Bai, Ying; Lekkerkerker-Teunissen, Karin; van der Hoek, Jan Peter

    2018-03-01

    The removal of bromate (BrO3-) as a by-product of ozonation in subsequent managed aquifer recharge (MAR) systems, specifically in anoxic nitrate (NO3-)-reducing zones, has so far gained little attention. In this study, batch reactors and columns were used to explore the influence of NO3- and increased assimilable organic carbon (AOC) due to ozonation pre-treatment on BrO3- removal in MAR systems. 8 m column experiments were carried out for 10 months to investigate BrO3- behavior in anoxic NO3--reducing zones of MAR systems. Anoxic batch experiments showed that an increase of AOC promoted microbial activity and corresponding BrO3- removal. A drastic increase of BrO3- biodegradation was observed in the sudden absence of NO3- in both batch reactors and columns, indicating that BrO3- and NO3- competed for biodegradation by denitrifying bacteria and NO3- was preferred as an electron acceptor under the simultaneous presence of NO3- and BrO3-. However, within 75 days' absence of NO3- in the anoxic column, BrO3- removal gradually decreased, indicating that the presence of NO3- is a precondition for denitrifying bacteria to reduce BrO3- in NO3--reducing anoxic zones. In the 8 m anoxic column set-up (retention time 6 days), the BrO3- removal achieved levels as low as 1.3 μg/L, starting at 60 μg/L (98% removal). Taken together, BrO3- removal is likely to occur in vicinity of NO3--reducing anoxic zones, so MAR systems following ozonation are potentially effective to remove BrO3-. Copyright © 2017. Published by Elsevier Ltd.

  18. Simultaneous determination of bromate, chlorite and haloacetic acids by two-dimensional matrix elimination ion chromatography with coupled conventional and capillary columns.

    Science.gov (United States)

    Teh, Hui Boon; Li, Sam Fong Yau

    2015-02-27

    A new, highly sensitive and reliable two-dimensional matrix elimination ion chromatography (IC) method was developed for simultaneous detection of bromate, chlorite and five haloacetic acids. This method combined the conventional IC in first dimension with capillary IC in the second dimension coupled with suppressed conductivity detection. The first dimension utilizes a high capacity column to partially resolve matrix from target analytes. By optimizing the cut window, the target analytes were selectively cut and trapped in a trap column through the use of a six-port valve, while the separated matrix were diverted to waste. The trapped target analytes were delivered on to the capillary column for further separation and detection. Temperature programming was used to improve selectivity in second dimension column to obtain complete resolution of the target analytes. Compared to the performance of one-dimensional IC, the two-dimensional approach resulted in a significant increase in sensitivity for all target analytes with limit of detection ranging from 0.30 to 0.64μg/L and provided more reliable analysis due to second column confirmation. Good linearity was obtained for all the target analytes with correlation coefficients >0.998. The proposed method was successfully applied to the determination of oxyhalides and haloacetic acids in various matrices with recoveries ranging from 90 to 116% and RSD less than 6.1%. The method allows direct injection of samples and the use of columns with different selectivity, thus significantly reduces the level of false positive results. The method is fully automated and simple, making it practical for routine monitoring of water quality. The satisfactory results also demonstrated that the two-dimensional matrix elimination method coupled with capillary IC is a promising approach for detection of trace substances in complex matrices. Copyright © 2015 Elsevier B.V. All rights reserved.

  19. Determination of trace formaldehyde by solid substrate-room temperature phosphorescence quenching method based on the rose bengal-potassium bromate-Tween-80 system

    Science.gov (United States)

    Liu, Jiaming; Yang, Tianlong; Zhu, Guohui; Chen, Hailing; Li, Pingping; Lin, Xuan; Huang, Xiaomei

    2008-03-01

    A new method for the determination of trace formaldehyde by solid substrate-room temperature phosphorescence quenching method has been proposed. It is based on the facts that rose bengal (R) can emit intense and stable room temperature phosphorescence on the solid substrate of filter paper (SS-RTP). Potassium bromate (KBrO 3) can oxidize R, which causes the quenching of RTP. In the presence of HCHO, it can react with KBrO 3 to form Br 2 and Br 2 can oxidize R, which causes smart quenching of RTP. The phosphorescence intensity (Δ Ip) is directly proportional to the concentration of HCHO. In the presence of Tween-80, the Δ Ip will be increased to 9.1 times higher than that without it. The linear range of this method is 0.016-1.6 fg spot -1 (corresponding concentration: 0.040-4.0 pg ml -1, 0.40 μl spot -1) with the detection limit of 4.5 ag spot -1 (corresponding concentration: 1.1 × 10 -14 g ml -1). The regression equation for working curve is Δ Ip = 136.6 + 28.28 mHCHO fg spot -1 ( r = 0.9935, n = 6). This method is sensitive, simple, rapid and has been applied to the determination of trace formaldehyde in real samples with satisfactory results. The mechanism of determination of trace formaldehyde by SS-RTP quenching method based on the rose bengal-KBrO 3-Tween-80 system is also discussed.

  20. Enhanced formation of bromate and brominated disinfection byproducts during chlorination of bromide-containing waters under catalysis of copper corrosion products.

    Science.gov (United States)

    Hu, Jun; Qiang, Zhimin; Dong, Huiyu; Qu, Jiuhui

    2016-07-01

    Copper corrosion products (CCPs) in water distribution pipes may catalyze the reactions among disinfectant, natural organic matter (NOM), and bromide (Br(-)). This study investigated the simultaneous formation of bromate (BrO3(-)) and brominated disinfection byproducts (Br-DBPs) during chlorination of Br(-)-containing waters in the presence of three CCPs (i.e., CuO, Cu2O, and Cu(2+)). In a synthetic water, both oxidant decay and BrO3(-) formation were enhanced by CCPs, whereas the presence of humic acid (HA) significantly inhibited BrO3(-) formation due to its competition for HOBr to form Br-DBPs. In the HOClBr(-)CuO system, the BrO3(-) yield increased obviously with increasing CuO dose and initial Br(-) concentration, while the catalytic formation of Br-DBPs was rather limited. A molar conversion (Br(-) to BrO3(-)) of 22.1% was observed under CuO catalysis, compared with little conversion in the absence of CuO. In the HOClBr(-)Cu2O/Cu(2+) systems, Cu2O or Cu(2+) mainly enhanced the formation of Br-DBPs, with enhancement ratios of 69.9% and 50.1%, respectively. The degree of enhancement on Br-DBPs formation became more apparent with increasing pH, while that on BrO3(-) formation reached maximal at pH 7.6. The catalytic formation of Br-DBPs and BrO3(-) by CCPs was also verified in three filtered real waters, although to a lesser extent because of the water matrix effect. In mechanism, the CCPs promoted the formation of BrO3(-) and Br-DBPs through catalyzing the HOBr disproportionation pathway and the reaction of HOBr toward HA, respectively. Copyright © 2016 Elsevier Ltd. All rights reserved.

  1. Cerium incorporated MCM-48 (Ce-MCM-48) as a catalyst to inhibit bromate formation during ozonation of bromide-containing water: Efficacy and mechanism.

    Science.gov (United States)

    Li, Weiwei; Lu, Xiaowei; Xu, Ke; Qu, Jiuhui; Qiang, Zhimin

    2015-12-01

    The composite mesoporous sieve Ce-MCM-48 (cerium incorporated MCM-48) with different Si/Ce molar ratios were synthesized hydrothermally and characterized with X-ray diffraction, X-ray photoelectron spectroscopy, BET surface area, and pHpzc. Results indicate that Ce-MCM-48, especially with a Si/Ce molar ratio of 66 (i.e., Ce66-MCM-48), could significantly inhibit bromate (BrO3(-)) formation during ozonation of Br(-)-containing water, achieving 91% of inhibition efficiency at pH 7.6 and 25 °C. An acidic or alkaline pH decreased the inhibition efficiency of Ce66-MCM-48 to some extent, but reaction temperature ranging from 15 to 30 °C had no significant impact. By comparing the bromine mass balance, aqueous O3 decomposition, and newly formed H2O2 between O3 and O3/Ce66-MCM-48 processes, the inhibition mechanism was proposed: Ce66-MCM-48 promoted aqueous O3 decomposition to generate hydroxyl radicals (OH) that could merge into H2O2, so the oxidative transformation of Br(-) and HOBr/OBr(-) by O3 and OH was primarily suppressed. The catalytic ability of Ce66-MCM-48 was continuously regenerated through the circulating reactions between Ce(III) and Ce(IV) occurring on the catalyst surface. Besides its inhibition on BrO3(-) formation, Ce66-MCM-48 could also enhance the degradation of refractory organic micropollutants. Because of these distinct merits, Ce66-MCM-48 has potential applications to water treatment by ozone. Copyright © 2015 Elsevier Ltd. All rights reserved.

  2. Kinetic-spectrophotometric determination of trace amounts of vanadium(V) based on its catalytic effect on the reaction of DBM-arsenazo and potassium bromate

    Science.gov (United States)

    Zhai, Qing-zhou; Zhang, Xiao-xia; Huang, Chong

    2008-03-01

    A simple and sensitive kinetic-spectrophotometric method is developed for the determination of trace vanadium(V), based on the catalytic effect of vanadium(V) on the oxidation of DBM-arsenazo by potassium bromate in 0.0138 mol l -1 phosphoric acid medium and at 100 °C in the presence of citric acid as activator. The absorbance is measured at 528 nm with the fixed-time method. The optimization of the operating conditions regarding concentrations of the reagents, temperature and interferences are also investigated. The working curve is linear over the concentration range 0-20 ng ml -1 of vanadium(V) with good precision and accuracy and the detection limit was down to 3.44 ng l -1. The relative standard deviation for a standard solution of 14 ng ml -1 is 0.28% ( n = 11). The apparent activity energies of the catalytic reaction and the non-catalytic reaction are 73.48, 113.5 kJ/mol, respectively. The proposed method proved highly sensitive, selective and relatively rapid for the assay of vanadium at low-level range of 0-20 ng ml -1 without any pre-concentration step. Thw method was applied to the determination of vanadium(V) in steels, rice, flour, cabbage, potato, fish, shrimp and tea samples with satisfactory results. The obtained results for the steel samples were excellent agreement with the standard reference values. The analytical results of the rice, flour, cabbage, potato, fish, shrimp and tea samples were excellent agreement with those of atomic absorption spectrometry. The recovery experiments have been made for the rice, flour, cabbage, potato, fish, shrimp and tea samples except the steels; excellent results were obtained. The relative standard deviations were over the range of 0.18-2.60% and the recoveries were over the range of 98.00-102.4%, respectively. The analytical results obtained were satisfactory.

  3. Effect of Potassium Bromate on the Liver of Adult Male Albino Rat and A Possible Protective Role of Vitamin C: Histological, Immunohistochemical, and Biochemical Study.

    Science.gov (United States)

    Bayomy, Naglaa A; Soliman, Gehan M; Abdelaziz, Eman Z

    2016-09-01

    Potassium bromate (KBrO3 ) is a food additive which is used primarily as a maturing agent for flour. It is proved as a toxic agent with significant reduction in the activities of antioxidant capacity. The therapeutic efficacy of vitamin C as antioxidant may provide a possible solution to KBrO3 mediated oxidative damage. Twenty four adult male albino rats were used to evaluate the protective role of vitamin C against KBrO3 induced hepatotoxicity and divided into four groups; Group 1 (control), Group 2: received 30 mg/Kg/day vitamin C orally for 4 weeks, Group 3: received 20 mg/Kg/dose KBrO3 orally twice weekly for 4 weeks and Group 4: received both KBrO3 and vitamin C. Liver specimens were processed for histological study by light and electron microscopes and stained immunohistochemically to detect glial fibriller acidic protein (GFAP). Serum levels of aspartate aminotransferase (AST) and alanine aminotransferase (ALT) were estimated as well as the levels of malondialdehyde (MDA), glutathione (GSH) and superoxide dismutase (SOD) activities in all dissected tissues were determined. KBrO3 induced histological alterations in the form of degeneration, cellular infiltration and significant increase in collagen deposition in portal tracts with a significant increase in immunoexpression of GFAP. Significant rise in serum levels of AST, ALT, and MDA in liver tissues were recorded. However, levels of GSH and SOD were significantly decreased. Most of these changes were improved by vitamin C treatment. In conclusion, vitamin C ameliorates the histological and biochemical alterations of the liver induced by KBrO3 . Anat Rec, 299:1256-1269, 2016. © 2016 Wiley Periodicals, Inc. © 2016 Wiley Periodicals, Inc.

  4. 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.

  5. Dinâmica complexa no sistema bromato/hipofosfito/acetona/manganês e ferroína Complex Dynamics in the bromate/hypophosphite/acetone/manganese and ferroin system

    Directory of Open Access Journals (Sweden)

    Gustavo Tokoro

    2007-01-01

    Full Text Available New chemical systems have been recently designed for the study of complex phenomena such as oscillatory dynamics in the temporal domain and spatiotemporal pattern formation. Systems derived from oscillators based on the chemistry of bromate are the most extensively studied, with the celebrated Belousov-Zhabotinsky (BZ reaction being the most popular example. Problems such as the formation of bubbles (CO2 and solid precipitate in the course of the reaction and the occurrence of simply short-lived oscillations under batch conditions are very common and, in some cases, compromise the use of some of these systems. It is investigated in this paper the dynamic behavior of the bromate/hypophosphite/acetone/dual catalyst system, which has been sugested as an interesting alternative to circumvent those inconvenients. In this work, manganese and ferroin are employed as catalysts and the complete system (BrO3-/H2PO2-/acetone/Mn(II-ferroin is studied under batch conditions. Temporal symmetry breaking was studied in a reactor under agitation by means of simultaneous records of the potential changes of platinum and Ag/AgBr electrodes, both measured versus a reversible hydrogen electrode. Additionally, spatio-temporal formation of target patterns and spiral waves were obtained when the oscillating mixture was placed in a quasi two-dimensional reactor.

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

    Science.gov (United States)

    Fotsing, Marcellin; Barbeau, Benoit; Prevost, Michele

    2011-01-01

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

  7. Graphene-modified Pd/C cathode and Pd/GAC particles for enhanced electrocatalytic removal of bromate in a continuous three-dimensional electrochemical reactor.

    Science.gov (United States)

    Mao, Ran; Zhao, Xu; Lan, Huachun; Liu, Huijuan; Qu, Jiuhui

    2015-06-15

    Bromate (BrO3(-)) is a carcinogenic and genotoxic contaminant commonly generated during ozonation of bromide-containing water. In this work, the reductive removal of BrO3(-) in a continuous three-dimensional electrochemical reactor with palladium-reduced graphene oxide modified carbon paper (Pd-rGO/C) cathode and Pd-rGO modified granular activated carbon (Pd-rGO/GAC) particles was investigated. The results indicated that the rGO sheets significantly promoted the electrochemical reduction of BrO3(-). With the enhanced electron transfer by rGO sheets, the electroreduction of H2O to atomic H* on the polarized Pd particles could be significantly accelerated, leading to a faster reaction rate of BrO3(-) with atomic H*. The synergistic effect of the Pd-rGO/C cathode and Pd-rGO/GAC particles were also exhibited. The atomic H* involved in various electroreduction processes was detected by electron spin resonance spectroscopy and its role for BrO3(-) reduction was determined. The performance of the reactor was evaluated in terms of the removal of BrO3(-) and the yield of Br(-) as a function of the GO concentration, Pd loading amount, current density, hydraulic residence time (HRT), and initial BrO3(-) concentration. Under the current density of 0.9 mA/cm(2), BrO3(-) with the initial concentration of 20 μg/L was reduced to be less than 6.6 μg/L at the HRT of 20 min. The BrO3(-) reduction was inhibited in the presence of dissolved organic matter. Although the precipitates generated from Ca(2+) and Mg(2+) in the tap water would cover the Pd catalysts, a long-lasting electrocatalytic activity could be maintained for the 30 d treatment. SEM and XPS analysis demonstrated that the precipitates were predominantly deposited onto the Pd-rGO/C cathode rather than the Pd-rGO/GAC particles. Copyright © 2015 Elsevier Ltd. All rights reserved.

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

    Energy Technology Data Exchange (ETDEWEB)

    Salimi, Abdollah [Department of Chemistry, University of Kurdistan, P.O. Box 416, Sanandaj (Iran, Islamic Republic of); Research Center for Nanotechnology, University of Kurdistan, P.O. Box 416, Sanandaj (Iran, Islamic Republic of)], E-mail: absalimi@uok.ac.ir; Kavosi, Begard [Department of Chemistry, University of Kurdistan, P.O. Box 416, Sanandaj (Iran, Islamic Republic of); Department of Chemistry, Arak University, P.O. Box, 38156-879 Arak (Iran, Islamic Republic of); Babaei, Ali [Department of Chemistry, Arak University, P.O. Box, 38156-879 Arak (Iran, Islamic Republic of); Hallaj, Rahman [Department of Chemistry, University of Kurdistan, P.O. Box 416, Sanandaj (Iran, Islamic Republic of)

    2008-06-16

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

  9. The Development of a New Inhibition Kinetic Spectrophotometric Method for the Determination of Phenylhydrazine Based on its Inhibitory Effect on Oxidation of Methyl Red by Bromate in Micellar Medium

    Directory of Open Access Journals (Sweden)

    Mohsen Keyvanfard

    2010-01-01

    Full Text Available A new, simple, sensitive and selective kinetic spectrophotometric method was developed for the determination of trace amounts of phenylhydrazine over the range of 0.02-0.30 μg/mL. The method is based on the inhibitory effect of phenylhydrazine on the oxidation of methyl red by bromate in acidic and micellar medium. The reaction was monitored spectrophotometrically by measuring the decrease in absorbance of methyl red at 518 nm with a fixed-time 0.5–2.0 min from initiation of the reaction..The relative standard deviation of 0.08 and 0.2 μg/mL phenylhydrazine was 1.7 and 2.4%, respectively. The method was applied to the determination of phenylhydrazine in water samples.

  10. Validação do método de determinação simultânea dos íons brometo e bromato por cromatografia iônica em águas de consumo humano Validation of simultaneous determination of bromides and bromates by ion chromatography in drinking water

    Directory of Open Access Journals (Sweden)

    Maria Edite Pinto Gonçalves

    2004-06-01

    Full Text Available European Directive (98/83/CE, compulsory after 2008, states that bromate in drinking water must be controlled at levels below 10 mg L-1. Supporting implementation of the Directive, the European Comission has established project SMT4-CT96 2134, in collaboration with various european institutions, aiming at the identification of the interferents to the current analytical method (Ionic Chromatography with Conductimetric Detection - IC/CD, their removal and the automation of pre-treatment and injection steps, as well as the development of alternative methods. EPAL, responsible for the water supply to a great deal of Portuguese regions, has taken steps to meet these requirements. Although not part of such project, this work (the result of a project conducted under a protocol of collaboration between EPAL SA and FCUL - Faculty of Sciences, University of Lisbon, reports on studies of usefulness to laboratories planning to monitor bromate in ozone treated waters, in conditions different from those described in EPA 300.1. Simultaneous determination of bromide is justified by its role as bromate precursor.

  11. Effect of operational and water quality parameters on conventional ozonation and the advanced oxidation process O3/H2O2: Kinetics of micropollutant abatement, transformation product and bromate formation in a surface water.

    Science.gov (United States)

    Bourgin, Marc; Borowska, Ewa; Helbing, Jakob; Hollender, Juliane; Kaiser, Hans-Peter; Kienle, Cornelia; McArdell, Christa S; Simon, Eszter; von Gunten, Urs

    2017-10-01

    The efficiency of ozone-based processes under various conditions was studied for the treatment of a surface water (Lake Zürich water, Switzerland) spiked with 19 micropollutants (pharmaceuticals, pesticides, industrial chemical, X-ray contrast medium, sweetener) each at 1 μg L-1. Two pilot-scale ozonation reactors (4-5 m3 h-1), a 4-chamber reactor and a tubular reactor, were investigated by either conventional ozonation and/or the advanced oxidation process (AOP) O3/H2O2. The effects of selected operational parameters, such as ozone dose (0.5-3 mg L-1) and H2O2 dose (O3:H2O2 = 1:3-3:1 (mass ratio)), and selected water quality parameters, such as pH (6.5-8.5) and initial bromide concentration (15-200 μg L-1), on micropollutant abatement and bromate formation were investigated. Under the studied conditions, compounds with high second-order rate constants kO3>104 M-1 s-1 for their reaction with ozone were well abated (>90%) even for the lowest ozone dose of 0.5 mg L-1. Conversely, the abatement efficiency of sucralose, which only reacts with hydroxyl radicals (OH), varied between 19 and 90%. Generally, the abatement efficiency increased with higher ozone doses and higher pH and lower bromide concentrations. H2O2 addition accelerated the ozone conversion to OH, which enables a faster abatement of ozone-resistant micropollutants. Interestingly, the abatement of micropollutants decreased with higher bromide concentrations during conventional ozonation due to competitive ozone-consuming reactions, except for lamotrigine, due to the suspected reaction of HOBr/OBr- with the primary amine moieties. In addition to the abatement of micropollutants, the evolution of the two main transformation products (TPs) of hydrochlorothiazide (HCTZ) and tramadol (TRA), chlorothiazide (CTZ) and tramadol N-oxide (TRA-NOX), respectively, was assessed by chemical analysis and kinetic modeling. Both selected TPs were quickly formed initially to reach a maximum concentration

  12. The Development of a New Kinetic Spectrophotometric Method for the Determination of Vanadium(V Based on its Catalytic Effect on the Oxidation of Malachite Green Oxalate by Bromate in Acidic and Micellar Medium

    Directory of Open Access Journals (Sweden)

    M. Keyvanfard

    2010-01-01

    Full Text Available A new, simple, sensitive and selective kinetic spectrophotometric method was developed for the determination of ultra trace amounts of vanadium(V. The method is based on the catalytic effect of vanadium(V on the oxidation of malachite green oxalate (MG by bromate in acidic and micellar medium. The reaction was monitored spectrophotometrically by measuring the decrease in the absorbance of malachite green oxalate (MG at 625 nm with a fixed-time method. The decrease in the absorbance of MG is proportional to the concentration of vanadium(V in the range of 1-100 ng/mL with a fixed time of 0.5-2 min from the initiation of the reaction. The limit of detection is 0.71 ng/mL of vanadium(V. The relative standard deviation for the determination of 5, 30, 50 ng/mL of vanadium(V was2.5% 2.6%, 2.4% and respectively. The method was applied to the determination of vanadium(V in water samples.

  13. Method for the fast determination of bromate, nitrate and nitrite by ultra performance liquid chromatography-mass spectrometry and their monitoring in Saudi Arabian drinking water with chemometric data treatment.

    Science.gov (United States)

    Khan, Mohammad Rizwan; Wabaidur, Saikh Mohammad; Alothman, Zeid Abdullah; Busquets, Rosa; Naushad, Mu

    2016-05-15

    A rapid, sensitive and precise method for the determination of bromate (BrO3(-)), nitrate (NO3(-)) and nitrite (NO2(-)) in drinking water was developed with Ultra performance Liquid Chromatography-Mass Spectrometry (UPLC-ESI/MS). The elution of BrO3(-), NO3(-) and NO2(-) was attained in less than two minutes in a reverse phase column. Quality parameters of the method were established; run-to-run and day-to-day precisions were <3% when analysing standards at 10 µg L(-1). The limit of detection was 0.04 µg NO2(-) L(-1) and 0.03 µg L(-1) for both NO3(-)and BrO3(-). The developed UPLC-ESI/MS method was used to quantify these anions in metropolitan water from Saudi Arabia (Jeddah, Dammam and Riyadh areas) and commercial bottled water (from well or unknown source) after mere filtration steps. The quantified levels of NO3(-) were not found to pose a risk. In contrast, BrO3(-) was found above the maximum contaminant level established by the US Environmental Protection Agency in 25% and 33% of the bottled and metropolitan waters, respectively. NO2(-) was found at higher concentrations than the aforementioned limits in 70% and 92% of the bottled and metropolitan water samples, respectively. Therefore, remediation measures or improvements in the disinfection treatments are required. The concentrations of BrO3(-), NO3(-) and NO2(-) were mapped with Principal Component analysis (PCA), which differentiated metropolitan water from bottled water through the concentrations of BrO3(-) and NO3(-) mainly. Furthermore, it was possible to discriminate between well water; blend of well water and desalinated water; and desalinated water. The point or source (region) was found to not be distinctive. Copyright © 2016. Published by Elsevier B.V.

  14. Immobilization of [Cu(bpy){sub 2}]Br{sub 2} complex onto a glassy carbon electrode modified with {alpha}-SiMo{sub 12}O{sub 40}{sup 4-} and single walled carbon nanotubes: Application to nanomolar detection of hydrogen peroxide and bromate

    Energy Technology Data Exchange (ETDEWEB)

    Salimi, Abdollah [Department of Chemistry, University of Kurdistan, P.O. Box 416, Sanandaj (Iran, Islamic Republic of); Research Center for Nanotechnology, University of Kurdistan, P.O. Box 416, Sanandaj (Iran, Islamic Republic of)], E-mail: absalimi@uok.ac.ir; Korani, Aazam; Hallaj, Rahman; Khoshnavazi, Roshan [Department of Chemistry, University of Kurdistan, P.O. Box 416, Sanandaj (Iran, Islamic Republic of); Hadadzadeh, Hasan [Department of Chemistry, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of)

    2009-03-02

    A simple procedure has been used for preparation of modified glassy carbon electrode with carbon nanotubes and copper complex. Copper complex [Cu(bpy){sub 2}]Br{sub 2} was immobilized onto glassy carbon (GC) electrode modified with silicomolybdate, {alpha}-SiMo{sub 12}O{sub 40}{sup 4-} and single walled carbon nanotubes (SWCNTs){sub .} Copper complex and silicomolybdate irreversibly and strongly adsorbed onto GC electrode modified with CNTs. Electrostatic interactions between polyoxometalates (POMs) anions and Cu-complex, cations mentioned as an effective method for fabrication of three-dimensional structures. The modified electrode shows three reversible redox couples for polyoxometalate and one redox couple for Cu-complex at wide range of pH values. The electrochemical behavior, stability and electron transfer kinetics of the adsorbed redox couples were investigated using cyclic voltammetry. Due to electrostatic interaction, copper complex immobilized onto GC/CNTs/{alpha}-SiMo{sub 12}O{sub 40}{sup 4-} electrode shows more stable voltammetric response compared to GC/CNTs/Cu-complex modified electrode. In comparison to GC/CNTs/Cu-complex the GC/CNTs/{alpha}-SiMo{sub 12}O{sub 40}{sup 4-} modified electrodes shows excellent electrocatalytic activity toward reduction H{sub 2}O{sub 2} and BrO{sub 3}{sup -} at more reduced overpotential. The catalytic rate constants for catalytic reduction hydrogen peroxide and bromate were 4.5({+-}0.2) x 10{sup 3} M{sup -1} s{sup -1} and 3.0({+-}0.10) x 10{sup 3} M{sup -1} s{sup -1}, respectively. The hydrodynamic amperommetry technique at 0.08 V was used for detection of nanomolar concentration of hydrogen peroxide and bromate. Detection limit, sensitivity and linear concentration range proposed sensor for bromate and hydrogen peroxide detection were 1.1 nM and 6.7 nA nM{sup -1}, 10 nM-20 {mu}M, 1 nM, 5.5 nA nM{sup -1} and 10 nM-18 {mu}M, respectively.

  15. Novel pre-treatments to control bromate formation during ozonation

    DEFF Research Database (Denmark)

    Antoniou, Maria; Sichel, Cosima; Andre, Klaus

    2017-01-01

    Worldwide water shortage increase and water quality depletion from microbial and chemical compounds, pose significant challenges for today’s water treatment industry. Both the development of new advanced oxidation technologies, but also the enhancement of existing conventional technologies......-treatments to ozonation of ground water. Each oxidant and NH4+ were added in a single stage or separately prior to ozonation. To the best of our knowledge, this is the first study that has tested all the above-mentioned oxidants for the same water matrix. Based on our results, the most promising pre-treatments were MnO4...

  16. catalyzed oxidation of some amino acids by acid bromate

    African Journals Online (AJOL)

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    Further, the product analysis by spotting techniques indicates the presence of aldehyde in the reaction mixture. So the product of oxidation should be the glycolic aldehyde (2-hydroxy ethanal) and α-hydroxy propionaldehyde (3- hydroxy propanal) for dl-serine and dl-threonine, respectively. The kinetic results were collected ...

  17. The mutagenic potentials of potassium bromate and some ...

    African Journals Online (AJOL)

    The mutant strains of the organism were examined in the presence or absence of rat liver metabolizing enzymes. The result showed that sodium bicarbonate, sodium benzoate and ammonium bicarbonate produced no mutant strain of the organism and no alteration in the phenotypic characteristics of the organism as ...

  18. Protective effects of rutin against potassium bromate induced nephrotoxicity in rats

    Directory of Open Access Journals (Sweden)

    Khan Rahmat

    2012-11-01

    Full Text Available Abstract Background Rutin, a polyphenolic flavonoid, was investigated for its protective effects against the KBrO3 induced renal injuries in rat. Methods Group I was control (untreated, group II was given saline 0.5 ml/kg bw (0.9% NaCl, group III was administered KBrO3 (20 mg/kg bw intragastric twice a week for four weeks. Rutin was administered to group VI (50 mg/kg bw and Group V (70 mg/kg bw along with KBrO3 (20 mg/kg bw while group VI was given rutin (70 mg/kg bw alone twice a week for four weeks. Protective effects of rutin on KBrO3-induced nephrotoxicity in rats were determined for biochemical parameter of urine, and serum, various antioxidant enzymes, DNA and histopathological damages in kidneys. Results The level of urinary red blood cells, leucocytes count, specific gravity, urea, creatinine and urobilinogen was increased (P3. Marked histopathological lesions, elevated DNA fragmentation and AgNORs count in renal tissues was determined. Activity of antioxidant enzymes; catalase, superoxide dismutase, glutathione peroxidase, glutathione-S-transferase, glutathione reductase, and reduced glutathione contents were decreased (P3 treatment in kidneys. DNA ladder assay was intimately related with the DNA fragmentation assay. Telomerase activity was found positive in the KBrO3 treated kidneys. Treatment with rutin effectively ameliorated the alterations in the studied parameters of rat. Rutin administration alone to rats did not exhibit any significant change in any of the parameters studied. Conclusion These results suggest that rutin works as an antioxidant in vivo by scavenging reactive oxygen species and this serves to prevent oxidative renal damage in rat treated with KBrO3.

  19. Protective effects of rutin against potassium bromate induced nephrotoxicity in rats

    Science.gov (United States)

    2012-01-01

    Background Rutin, a polyphenolic flavonoid, was investigated for its protective effects against the KBrO3 induced renal injuries in rat. Methods Group I was control (untreated), group II was given saline 0.5 ml/kg bw (0.9% NaCl), group III was administered KBrO3 (20 mg/kg bw) intragastric twice a week for four weeks. Rutin was administered to group VI (50 mg/kg bw) and Group V (70 mg/kg bw) along with KBrO3 (20 mg/kg bw) while group VI was given rutin (70 mg/kg bw) alone twice a week for four weeks. Protective effects of rutin on KBrO3-induced nephrotoxicity in rats were determined for biochemical parameter of urine, and serum, various antioxidant enzymes, DNA and histopathological damages in kidneys. Results The level of urinary red blood cells, leucocytes count, specific gravity, urea, creatinine and urobilinogen was increased (P<0.01) whereas creatinine clearance was reduced. Serum level of protein, albumin, globulin, nitrite, creatinine and blood urea nitrogen (BUN) was significantly increased (P<0.01) by KBrO3. Marked histopathological lesions, elevated DNA fragmentation and AgNORs count in renal tissues was determined. Activity of antioxidant enzymes; catalase, superoxide dismutase, glutathione peroxidase, glutathione-S-transferase, glutathione reductase, and reduced glutathione contents were decreased (P<0.01) while thiobarbituric acid reactive substances were increased (P<0.01) with KBrO3 treatment in kidneys. DNA ladder assay was intimately related with the DNA fragmentation assay. Telomerase activity was found positive in the KBrO3 treated kidneys. Treatment with rutin effectively ameliorated the alterations in the studied parameters of rat. Rutin administration alone to rats did not exhibit any significant change in any of the parameters studied. Conclusion These results suggest that rutin works as an antioxidant in vivo by scavenging reactive oxygen species and this serves to prevent oxidative renal damage in rat treated with KBrO3. PMID:23116356

  20. Chemical wave in the un-illuminated aminophenol-bromate beads system

    Science.gov (United States)

    Harati, Mohammad

    2009-07-01

    We report observation of slow oscillations and slow waves in the aminophenol system. The system with slow oscillations in the stirred batch reactor does not always exhibit slow waves. The unperturbed system exhibits more than 2 days of wave activity, while the perturbed system shows about 5 days of wave activity. The longest lifetime of wave propagation stage and quiescent window were 30 and 11 h, respectively.

  1. Potassium bromate causes cell lysis and induces oxidative stress in human erythrocytes.

    Science.gov (United States)

    Ahmad, Mir Kaisar; Amani, Samreen; Mahmood, Riaz

    2014-02-01

    In the present study, we have studied the effect of KBrO3 on human erythrocytes under in vitro conditions. Erythrocytes were isolated from the blood of healthy nonsmoking volunteers and incubated with different concentrations of KBrO3 at 37°C for 60 min. This resulted in marked hemolysis in a KBrO3 -concentration dependent manner. Lysates were prepared from KBrO3 -treated and control erythrocytes and assayed for various parameters. KBrO3 treatment caused significant increase in protein oxidation, lipid peroxidation, hydrogen peroxide levels, and decrease in total sulfhydryl content, which indicates induction of oxidative stress in human erythrocytes. Methemoglobin levels and methemoglobin reductase activity were significantly increased while the total antioxidant power of lysates was greatly reduced upon KBrO3 treatment. Intracellular production of reactive oxygen species increased in a dose dependent manner. Exposure of erythrocytes to KBrO3 also caused decrease in the activities of catalase, glutathione peroxidase, thioredoxin reductase, glucose 6-phosphate dehydrogenase and glutathione reductase whereas the activities of Cu-Zn superoxide dismutase and glutathione-S-transferase were increased. These results show that KBrO3 induces oxidative stress in human erythrocytes through the generation of reactive oxygen species and alters the cellular antioxidant defense system. Copyright © 2011 Wiley Periodicals, Inc., A Wiley Company.

  2. Evaluation of pre-treatments for inhibiting bromate formation during ozonation

    DEFF Research Database (Denmark)

    Antoniou, Maria; Andersen, Henrik Rasmus

    2011-01-01

    This study compared several pre-treatment methods for inhibiting BrO3- formation during ozonation of tap water, from the DTU campus, including H2O2 addition (perozone), pH-depression, NH4+ and Cl2/NH4+ addition. At the same time, the inhibition of atrazine and carbamazepine removal was evaluated...... close to the 10 μg/L limit, however atrazine removal did not exceed 75%. Carbamazepine was completely removed under all the tested experimental conditions with the 3.5 mg/L O3 dose....

  3. Spectrophotometric determination of lansoprazole in pharmaceuticals using bromate-bromide mixture based on redox and complexation reactions

    OpenAIRE

    Basavaiah, K.; Ramakrishna, V.; U. R. Anil Kumar; Somashekar, B. C.

    2007-01-01

    Two sensitive spectrophotometric methods are described for the determination of lansoprazole (LPZ) in bulk drug and in capsule formulation. The methods are based on the oxidation of lansoprazole by insitu generated bromine followed by determination of unreacted bromine by two different reaction schemes. In one procedure (method A), the residual bromine is treated with excess of iron (II), and the resulting iron (III) is complexed with thiocyanate and measured at 470 nm. The second approach (m...

  4. Termination of nanoscale zero-valent iron reactivity by addition of bromate as a reducing reactivity competitor

    DEFF Research Database (Denmark)

    Mines, Paul D.; Kaarsholm, Kamilla Marie Speht; Droumpali, Ariadni

    2017-01-01

    an appropriate way to terminate the reactivity of any nZVI-containing material for a practical experimental procedure. In this study, bimetallic Ni/Fe-NPs were prepared to enhance overall reduction kinetics owing to the catalytic reactivity of nickel on the surface of nZVI. We have tested several chemical...

  5. Sensitive Spectrophotometric Determination of Atenolol in Pharmaceutical Formulations Using Bromate-Bromide Mixture as an Eco-Friendly Brominating Agent

    Directory of Open Access Journals (Sweden)

    Kudige N. Prashanth

    2012-01-01

    Full Text Available Three simple and sensitive spectrophotometric methods are proposed for the determination of atenolol (ATN in bulk drug and tablets. The methods are based on the bromination of ATN by the bromine generated in situ by the action of the acid on the bromate–bromide mixture followed by the determination of unreacted bromine by reacting with a fixed amount of either meta-cresol purple (MCP and measuring the absorbance at 540 nm (method A and 445 nm (method B or erioglaucine (EGC and measuring the absorbance at 630 nm (method C. Beer's law is valid within the concentration ranges of 1.0–20.0, 2.0–40.0 and 1.0–8.0 μg/mL for method A, method B and method C, respectively. The calculated molar absorptivities were found to be 1.20×104, 4.51×103 and 3.46×104  L/mol⋅cm for method A, method B and method C, respectively. Sandell’s sensitivity values, correlation coefficients, limits of detection and quantification are also reported. Recovery results were statistically compared with those of a reference method by applying Student’s t- and F-test. The novelty of the present study is the measurement of two different colors using MCP, that is, red-pink color of MCP in acid medium at 540 nm and yellowish-orange color of brominated MCP at 445 nm.

  6. A NEW, SENSITIVE, AND SELECTIVE METHOD FOR DETERMINING SUB-MG/L LEVELS OF BROMATE IN DRINKING WATER. (R825952)

    Science.gov (United States)

    The perspectives, information and conclusions conveyed in research project abstracts, progress reports, final reports, journal abstracts and journal publications convey the viewpoints of the principal investigator and may not represent the views and policies of ORD and EPA. Concl...

  7. Electrodeposition of silver particles from alkaline aqueous solutions and their electrocatalytic activity for the reduction of nitrate, bromate and chlorite ions

    Energy Technology Data Exchange (ETDEWEB)

    Casella, Innocenzo G., E-mail: innocenzo.casella@unibas.i [Dipartimento di Chimica dell' Universita degli Studi della Basilicata, Via N. Sauro 85, 85100 Potenza (Italy); Ritorti, Mariagiovanna [Dipartimento di Chimica dell' Universita degli Studi della Basilicata, Via N. Sauro 85, 85100 Potenza (Italy)

    2010-09-01

    A pulsed electrochemical method was used for the preparation of silver deposit onto glassy carbon surfaces from an alkaline medium containing ammonia ligand. The morphology of the silver deposit, obtained under pulsed and cyclic conditions was examined and compared using the scanning electron microscopy (SEM) technique. From the experimental evidences, it can be inferred that pulsed method induces a favourable dendritic growth of silver particles, while deposited films obtained under cyclic voltammetry appear formed of globular particles with well regular and defined surface geometry. The electroanalytical performance of the deposited silver, towards the electroreduction of NO{sub 3}{sup -}, BrO{sub 3}{sup -} and ClO{sub 2}{sup -} ions, using cyclic voltammetry and chronoamperometry technique, was evaluated. Interesting analytical results, in terms of sensitivity and temporal reproducibility, in alkaline medium and under constant applied potentials (i.e., -1.45 and -0.6 V vs. SCE), were obtained.

  8. The Effect of Msh2 Knockdown on Toxicity Induced by tert-Butyl-hydroperoxide, Potassium Bromate, and Hydrogen Peroxide in Base Excision Repair Proficient and Deficient Cells

    Directory of Open Access Journals (Sweden)

    N. Cooley

    2013-01-01

    Full Text Available The DNA mismatch repair (MMR and base excision repair (BER systems are important determinants of cellular toxicity following exposure to agents that cause oxidative DNA damage. To examine the interactions between these different repair systems, we examined whether toxicity, induced by t-BOOH and KBrO3, differs in BER proficient (Mpg+/+, Nth1+/+ and deficient (Mpg−/−, Nth1−/− mouse embryonic fibroblasts (MEFs following Msh2 knockdown of between 79 and 88% using an shRNA expression vector. Msh2 knockdown in Nth1+/+ cells had no effect on t-BOOH and KBrO3 induced toxicity as assessed by an MTT assay; knockdown in Nth1−/− cells resulted in increased resistance to t-BOOH and KBrO3, a result consistent with Nth1 removing oxidised pyrimidines. Msh2 knockdown in Mpg+/+ cells had no effect on t-BOOH toxicity but increased resistance to KBrO3; in Mpg−/− cells, Msh2 knockdown increased cellular sensitivity to KBrO3 but increased resistance to t-BOOH, suggesting a role for Mpg in removing DNA damage induced by these agents. MSH2 dependent and independent pathways then determine cellular toxicity induced by oxidising agents. A complex interaction between MMR and BER repair systems, that is, exposure dependent, also exists to determine cellular toxicity.

  9. The Effect of Msh2 Knockdown on Toxicity Induced by tert-Butyl-hydroperoxide, Potassium Bromate, and Hydrogen Peroxide in Base Excision Repair Proficient and Deficient Cells

    Science.gov (United States)

    Cooley, N.; Elder, R. H.; Povey, A. C.

    2013-01-01

    The DNA mismatch repair (MMR) and base excision repair (BER) systems are important determinants of cellular toxicity following exposure to agents that cause oxidative DNA damage. To examine the interactions between these different repair systems, we examined whether toxicity, induced by t-BOOH and KBrO3, differs in BER proficient (Mpg +/+, Nth1 +/+) and deficient (Mpg −/−, Nth1 −/−) mouse embryonic fibroblasts (MEFs) following Msh2 knockdown of between 79 and 88% using an shRNA expression vector. Msh2 knockdown in Nth1 +/+ cells had no effect on t-BOOH and KBrO3 induced toxicity as assessed by an MTT assay; knockdown in Nth1 −/− cells resulted in increased resistance to t-BOOH and KBrO3, a result consistent with Nth1 removing oxidised pyrimidines. Msh2 knockdown in Mpg +/+ cells had no effect on t-BOOH toxicity but increased resistance to KBrO3; in Mpg −/− cells, Msh2 knockdown increased cellular sensitivity to KBrO3 but increased resistance to t-BOOH, suggesting a role for Mpg in removing DNA damage induced by these agents. MSH2 dependent and independent pathways then determine cellular toxicity induced by oxidising agents. A complex interaction between MMR and BER repair systems, that is, exposure dependent, also exists to determine cellular toxicity. PMID:23984319

  10. Removal of Pesticides and Inorganic Contaminants in Anaerobic and Aerobic Biological Contactors

    Science.gov (United States)

    This presentation contains data on the removal of pesticides (acetochlor, clethodim, dicrotophos), ammonia, nitrate, bromate and perchlorate through aerobic and anaerobic biological treatment processes.

  11. Bromide en bromaat in drink- en oppervlaktewater

    NARCIS (Netherlands)

    Versteegh JFM; Neele J; Cleven RFMJ; Smeenk JGMM; Westra R

    1993-01-01

    This report describes the results of research done in 1992 after the occurrence of bromate during the production of drinking water. A survey was carried out among five drinking water plants ; surface waters of the rivers Rhine and Meuse were included as well. Bromate is only occasionnally present

  12. Oxyhalogen-Sulfur Chemistry: Kinetics and Mechanism of Oxidation ...

    African Journals Online (AJOL)

    The oxidation of N-acetylthiourea (ACTU) by acidic bromate has been studied by observing formation of bromine in excess bromate conditions. The reaction displays an induction period before formation of bromine. The stoichiometry of the reaction was determined to be 4:3: 4BrO3 ...

  13. Download this PDF file

    African Journals Online (AJOL)

    Summary. Okeniyi JAO, Aladekomo TA, Oyelami 0A. Acute Renal Failure following Accidental. Potassium Bromate Poisoning: A Case Report. Nigerian journal of Paediatrics 2003; 30:150. Accidental poisoning is common in children. Potassium bromate is a commonly used additive and raising agent in many edibles ...

  14. OZONE CONTACTOR FLOW VISUALIZATION AND CHARACTERIZATION USING 3-DIMENSIONAL LASER INDUCED FLUORESCENCE

    Science.gov (United States)

    Hydrodynamics of ozone contactors have a crucial impact on efficient inactivation of pathogens such as Cryptosporidium as well as control of disinfection byproducts such as bromate. Improper mixing behaviors including short-circuiting, internal recirculation and presence...

  15. dbs-arsenazo

    African Journals Online (AJOL)

    IV) catalyzes the discoloring reaction of DBS-arsenazo oxidized by potassium bromate, a new catalytic kinetic spectrophotometric method for the determination of trace titanium (IV) was developed. The linear range of the determination of ...

  16. Combination of ozonation and photocatalysis for purification of aqueous effluents containing formic acid as probe pollutant and bromide ion.

    Science.gov (United States)

    Parrino, F; Camera-Roda, G; Loddo, V; Palmisano, G; Augugliaro, V

    2014-03-01

    The treatment by advanced oxidation processes (AOPs) of waters contaminated by organic pollutants and containing also innocuous bromide ions may generate bromate ions as a co-product. In the present work heterogeneous photocatalysis and ozonation have individually been applied and in combination (integrated process) to degrade the organic compounds in water containing also bromide anions. The results show that: i) the sole photocatalysis does not produce bromate ions and in the case of its presence, it is able to reduce bromate to innocuous bromide ions; ii) the integration of photocatalysis and ozonation synergistically enhances the oxidation capabilities; and iii) in the integrated process bromate ions are not produced as long as some oxidizable organics are present. Copyright © 2013 Elsevier Ltd. All rights reserved.

  17. Dinâmica oscilatória em sistemas contendo bromato e 1,4-ciclo-hexanodiona em meio ácido: I. Efeito da temperatura

    Directory of Open Access Journals (Sweden)

    Hyrla C. L. Oliveira

    2012-01-01

    Full Text Available We present in this work the influence of temperature on the dynamics of homogeneous chemical systems containing bromate and 1,4-cyclohexanedione (1,4-CHD in acidic media. In particular, the following systems were studied: bromate/1,4-CHD/acid, bromate/1,4-CHD/ferroin/acid and bromate/1,4-CHD/trisbipyridine ruthenium/acid. Investigations were carried out by means of an electrochemical probe, at five temperatures between 5 and 45 °C. Activation energies (Ea were estimated in different ways for the pre-oscillatory and oscillatory regimes. In any case, the Ea was found to depend on the catalyst, composition and initial concentrations. In addition, it was observed that ferroin and trisbipyridine ruthenium act as catalysts only during the transition between the induction period and oscillatory regime.

  18. Kinetics and Mechanism of Oxidation of N-acetylthiourea by ...

    African Journals Online (AJOL)

    NICOLAAS

    The oxidation of N-acetylthiourea (ACTU) by acidic bromate has been studied by observing formation of bromine in excess bromate conditions. The reaction displays an induction period before formation of bromine. The stoichiometry of the reaction was determined to be 4:3: 4BrO3. – + 3(CH3CO)NH(NH2)C=S + 3H2O ...

  19. The Effect of Ozonation Process on Bromide-Containing Groundwaters in Bandung Area and Its Surroundings

    Directory of Open Access Journals (Sweden)

    Mindriany Syafila

    2012-11-01

    Full Text Available Disinfection process was applied as the last step of the water treatment to kill pathogenic bacteria in the water. However, according to several studies, the ozonation disinfection process could form undesired by-products. One of the by-products potentially affecting human life is bromate produced from bromide ionic-containing water. This study was carried out to examine the effect of raw water characteristics and pH on bromate formation. Also, the performance of bromate formation for a period of exposure time was analyzed. Raw waters taken from four different areas around Bandung were exposed to ozone introduced to a reactor with a flow rate of 2 L/min. The pH of the raw waters varied from 4, 7 to 10. The results show that there was no evidence of an initial bromide ion concentration, whereas a change in pH value gives a significantly different outcome. In acidic condition (pH of 4 the bromate formation tends to decrease, whereas when the pH value increases to a pH of 10, the bromate formation increases. Therefore, for drinking water with a neutral pH, when bromide ions are detected in the raw water, the drinking water may be toxic due to the presence of bromate.

  20. Determinação de bromato em melhoradores de farinha por cromatografia de troca iônica com detecção espectrofotométrica Bromate determination in flour improvers by ion exchange chromatography with spectrophotometric detection

    Directory of Open Access Journals (Sweden)

    Rogério Marcos Dallago

    2005-08-01

    Full Text Available KBrO3 is registered by the FAO/OMS as a genotoxic and carcinogenic compound. In spite of this, KBrO3 is still employed by Brazilian bakeries. Nowadays ion exchange chromatography (IEC is the most rapid and trustful method for BrO3- analysis. When at high concentrations, chloride ions can interfere in the BrO3- analysis, if the detection is performed by electrical conductivity. On the other hand, spectrophotometric detection, presented here is based on the absorption of BrO3- in the ultraviolet region (210 - 230 nm where the absortion of chloride ions is very low, thus making possible the qualitative and quantitative analysis of BrO3- in flour improver samples.

  1. DEMONSTRATION OF THE HIPOX ADVANCED OXIDATION TECHNOLOGY FOR THE TREATMENT OF MTBE-CONTAMINATED GROUNDWATER

    Science.gov (United States)

    The HiPOx technology is an advanced oxidation process that incorporates high-precision delivery of ozone and hydrogen peroxide to chemically destroy organic contaminants with the promise of minimizing bromate formation. A MTBE-contaminated groundwater from the Ventura County Nav...

  2. Formation of hazardous inorganic by-products during electrolysis of seawater as a disinfection process for desalination.

    Science.gov (United States)

    Oh, Byung Soo; Oh, Sang Guen; Hwang, Youn Young; Yu, Hye-Weon; Kang, Joon-Wun; Kim, In S

    2010-11-01

    From our previous study, an electrochemical process was determined to be a promising tool for disinfection in a seawater desalination system, but an investigation on the production of several hazardous by-products is still required. In this study, a more intensive exploration of the formation patterns of perchlorate and bromate during the electrolysis of seawater was conducted. In addition, the rejection efficiencies of the targeted by-products by membrane processes (microfiltration and seawater reverse osmosis) were investigated to uncover the concentrations remaining in the final product from a membrane-based seawater desalination system for the production of drinking water. On the electrolysis of seawater, perchlorate did not provoke any problem due to the low concentrations formed, but bromate was produced at a much higher level, resulting in critical limitation in the application of the electrochemical process to the desalination of seawater. Even though the formed bromate was rejected via microfiltration and reverse osmosis during the 1st and 2nd passes, the residual concentration was a few orders of magnitude higher than the USEPA regulation. Consequently, it was concluded that the application of the electrochemical process to seawater desalination cannot be recommended without the control of bromate. Copyright © 2010 Elsevier B.V. All rights reserved.

  3. Author Details

    African Journals Online (AJOL)

    Olojo, Rotimi. Vol 55 (2002) - Articles Complex Kinetics in the Reaction of Taurine with Aqueous Bromine and Acidic Bromate : A Possible Cytoprotective Role against Hypobromous Acid Abstract PDF. ISSN: 0379-4350. AJOL African Journals Online. HOW TO USE AJOL... for Researchers · for Librarians · for Authors · FAQ's ...

  4. Author Details

    African Journals Online (AJOL)

    Mundoma, Claudius. Vol 55 (2002) - Articles Complex Kinetics in the Reaction of Taurine with Aqueous Bromine and Acidic Bromate : A Possible Cytoprotective Role against Hypobromous Acid Abstract PDF. ISSN: 0379-4350. AJOL African Journals Online. HOW TO USE AJOL... for Researchers · for Librarians · for Authors.

  5. South African Journal of Chemistry - Vol 55 (2002)

    African Journals Online (AJOL)

    On-line Determination of Hydrochloric Acid in Process Effluent Streams by Potentiometric Sequential Injection Acid-Base Titration · EMAIL FREE FULL TEXT EMAIL ... Complex Kinetics in the Reaction of Taurine with Aqueous Bromine and Acidic Bromate : A Possible Cytoprotective Role against Hypobromous Acid · EMAIL ...

  6. CATALYTIC KINETIC SPECTROPHOTOMETRIC DETERMINATION ...

    African Journals Online (AJOL)

    Based on the property that in 0.12 M sulfuric acid medium titanium(IV) catalyzes the discoloring reaction of DBS-arsenazo oxidized by potassium bromate, a new catalytic kinetic spectrophotometric method for the determination of trace titanium (IV) was developed. The linear range of the determination of titanium is

  7. Kinetics and mechanism of oxidation of glycine by iron(III)–1,10 ...

    Indian Academy of Sciences (India)

    Unknown

    of oxidation are reported to be formaldehyde, car- bon dioxide and ammonia with K2S2O8, KMnO4, po- tassium bromate and aquomanganese(III), while the products obtained with ferricyanide are keto acid and ammonia and with Mn(III) sulphate, formalde- hyde, glyoxalic acid, carbon dioxide and ammonia. In an attempt to ...

  8. Selenium dioxide catalysed oxidation of acetic acid hydrazide by ...

    Indian Academy of Sciences (India)

    Selenium dioxide catalysed acetic acid hydrazide oxidation by bromate was studied in hydrochloric acid medium. The order in oxidant concentration, substrate and catalyst were found to be unity. Increasing hydrogen ion concentration increases the rate of the reaction due to protonation equilibria of the oxidant.

  9. Perspectives

    Indian Academy of Sciences (India)

    Prakash

    The processes start again. The reaction will stop when the amount of citric acid and bromate is exhausted. In his early writings, A M Zhabotinsky showed that the liberation of free bromine was not essential for the Belousov reaction. Belousov felt that he had discovered a significant phenomenon. 'The reaction described here ...

  10. Enzyme activities and histopathology of selected tissues in rats ...

    African Journals Online (AJOL)

    The effect of chronic administration of potassium bromate (KBrO3), a flour improver, on some 'marker' enzymes of rat cellular system was investigated. The levels of these enzymes were measured progressively in the kidney, liver and small intestine, 24h after days 1, 3, 5, 10, 15 and 20 following the administration of ...

  11. Bulletin of Materials Science | Indian Academy of Sciences

    Indian Academy of Sciences (India)

    Home; Journals; Bulletin of Materials Science. V Surender. Articles written in Bulletin of Materials Science. Volume 24 Issue 6 December 2001 pp 665-669 Single Crystals. Surface studies on as-grown (111) faces of sodium bromate crystals · K Kishan Rao V Surender · More Details Abstract Fulltext PDF. Single crystals of ...

  12. 40 CFR 141.64 - Maximum contaminant levels for disinfection byproducts.

    Science.gov (United States)

    2010-07-01

    ... the Act, hereby identifies the following as the best technology, treatment techniques, or other means... treatment process to reduce production of bromate Chlorite Control of treatment processes to reduce disinfectant demand and control of disinfection treatment processes to reduce disinfectant levels (b) TTHM and...

  13. Download this PDF file

    African Journals Online (AJOL)

    Femi J. Olorunniji

    2015-03-31

    Mar 31, 2015 ... Fitoterapia 77(4):324-326. Khan, N., Sharma, S. and Sultana, S. (2004) Attenuation of potassium bromate-induced nephrotoxicity by coumarin (1,2- benzopyrone) in Wistar rats: chemoprevention against free radical-mediated renal oxidative stress and tumor promotion response. Redox report 9(1):19-28.

  14. Acute Renal Failure following Accidental Potassium

    African Journals Online (AJOL)

    . Summary. Okeniyi JAO, Aladekomo TA, Oyelami 0A. Acute Renal Failure following Accidental. Potassium ... Serum Electrvgyte and Urea lef in the Patient '. ' D91 4 Dry 7 D49! ... determination of bromate residues with accuracy in a variety of ...

  15. Modulation of enzyme activities following the coadministration of ...

    African Journals Online (AJOL)

    Nonetheless, acid phosphatase (ACP) activity was not appreciably affected in both tissues. Corresponding significant increases (p<0.05) in activity of these enzymes in the serum was observed. However, unexpected high values of enzyme activities in both tissues when both potassium bromate and chloroquine were ...

  16. SPECTROPHOTOMETRIC DETERMINATION OF NITRITE BY ITS ...

    African Journals Online (AJOL)

    Preferred Customer

    KEY WORDS: Nitrite, Catalytic effect, Congo red, Spectrophotometry, Drinking water. INTRODUCTION ... such as high sensitivity, low detection limits, good selectivity, rapid analysis and inexpensive instrumentation. ... Determination of nitrite by its catalytic effect on oxidation of congo red with bromate. Bull. Chem. Soc.

  17. 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

  18. 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.

  19. Complex Kinetics in the Reaction of Taurine with Aqueous Bromine ...

    African Journals Online (AJOL)

    Complex Kinetics in the Reaction of Taurine with Aqueous. Bromine and Acidic Bromate: A Possible Cytoprotective. Role against Hypobromous Acid. Reuben H. Simoyi1*, Kevin Streete2, Claudius Mundoma2 and Rotimi Olojo2. 1Department of Chemistry, University of Cape Town, Rondebosch, 7700 South Africa.

  20. Kinetic-Spectrophotometric Determination of Iodide Based on its Inhibitory Effect on the Decolorization Reaction of Methyl Orange

    Directory of Open Access Journals (Sweden)

    Reyhaneh Rahnama Kozani

    2009-01-01

    Full Text Available A simple, sensitive, rapid and reliable method has been developed for spectrophotometric determination of iodide based on its inhibition effect on the redox reaction between bromate and hydrochloric acid. The decolorization of methyl orange by the reaction products was used to monitor the reaction spectrophotometrically at 525 nm. The variables affecting the rate of the reaction were investigated. Under the optimum conditions, the limit of detection is 1.5 × 10-7 mol L-1 and calibration range is 2.0 × 10-6–1.3 × 10-4 mol L-1 of iodide. The linearity range of the calibration graph is depends on bromate concentration. The relative standard deviation of ten-replication determination of 8.2 × 10-5 mol L-1 iodide was 1.4%. The proposed method was applied to the determination of iodide in natural water samples with satisfactory results.

  1. The Effect of Different Boiling and Filtering Devices on the Concentration of Disinfection By-Products in Tap Water

    OpenAIRE

    Glòria Carrasco-Turigas; Villanueva, Cristina M.; Fernando Goñi; Panu Rantakokko; Nieuwenhuijsen, Mark J.

    2013-01-01

    Disinfection by-products (DBPs) are ubiquitous contaminants in tap drinking water with the potential to produce adverse health effects. Filtering and boiling tap water can lead to changes in the DBP concentrations and modify the exposure through ingestion. Changes in the concentration of 4 individual trihalomethanes (THM4) (chloroform (TCM), bromodichloromethane (BDCM), dibromochloromethane (DBCM), and bromoform (TBM)), MX, and bromate were tested when boiling and filtering high bromine-conta...

  2. Porovnání metod pro stanovení prokainu v léčivých přípravcích

    OpenAIRE

    Baptistová, Adéla

    2014-01-01

    The aim of this bachelor thesis was to compare four analytical methods for determination of procaine hydrochloride in medical formulations in terms of precision and measurement trueness, and its time, and financial cost. The selected methods are: titration with potassium bromate, titration with sodium nitrite, UV spectrophotometry, VIS spectrophotometry. Three injection solutions of different concentrations (0.2%, 0.5%, and 1.0% of procaine) were analysed. VIS spectrophotometry provides the m...

  3. Minutes of the Explosives Safety Seminar (16th), Held at the Diplomat Hotel, Hollywood, Florida on 24-26 September 1974. Volume 2

    Science.gov (United States)

    1974-09-26

    peroxide, sodium hypochlorite, chlorine gas, potassium persulfate, potassium bromate, sodium perborate and air (catalyzed and uncatalyzed). Although the...for destruction of that same agent. GB is de- stroyed by chemically neutralizing it with caustic ( sodium hydroxide). This reduces the agent to a brine...phenols, sodium , sulfate, BOD (biological oxygen demand) and suspended solids as parameters for primer wastes. Table III presents the industrial

  4. Belousov-Zhabotinsky oscillatory reaction. Kinetics of malonic acid decomposition

    Directory of Open Access Journals (Sweden)

    LJILJANA KOLAR-ANIC

    2000-10-01

    Full Text Available The kinetics of the Belousov-Zhabotinsky (BZ oscillatory reaction was analyzed. With this aim, the time evolution of a reaction mixture composed of malonic acid, bromate, sulfuric acid and cerium(III was studied at 298 K. Pseudo-first order kinetics with respect to malonic acid as the species undergoing decomposition with a corresponding rate constant, k = 7.5×10-3 min-1, was found.

  5. Protective effects of Sonchus asper against KBrO3 induced lipid peroxidation in rats

    Directory of Open Access Journals (Sweden)

    Khan Rahmat Ali

    2012-11-01

    Full Text Available Abstract Background Sonchus asper is traditionally used in Pakistan for the treatment of reproductive dysfunction and oxidative stress. The present investigation was aimed to evaluate chloroform extract of Sonchus asper (SACE against potassium bromate-induced reproductive stress in male rats. Methods 20 mg/kg body weight (b.w. potassium bromate (KBrO3 was induced in 36 rats for four weeks and checked the protective efficacy of SACE at various hormonal imbalances, alteration of antioxidant enzymes, and DNA fragmentation levels. High performance chromatography (HPLC was used for determination of bioactive constituents responsible. Results The level of hormonal secretion was significantly altered by potassium bromate. DNA fragmentation%, activity of antioxidant enzymes; catalase (CAT, peroxidase (POD, superoxide dismutase (SOD and phase II metabolizing enzymes viz; glutathione reductase (GSR, glutathione peroxidase (GSHpx, glutathione-S-tansase (GST and reduced glutathione (GSH was decreased while hydrogen per oxide contents and thiobarbituric acid reactive substances (TBARS were increased with KBrO3 treatment. Treatment with SACE effectively ameliorated the alterations in the biochemical markers; hormonal and molecular levels while HPLC characterization revealed the presence of catechin, kaempferol, rutin and quercetin. Conclusion Protective effects of Sonchus asper vs. KBrO3 induced lipid peroxidation might be due to bioactive compound present in SACE.

  6. The Effect of Different Boiling and Filtering Devices on the Concentration of Disinfection By-Products in Tap Water

    Directory of Open Access Journals (Sweden)

    Glòria Carrasco-Turigas

    2013-01-01

    Full Text Available Disinfection by-products (DBPs are ubiquitous contaminants in tap drinking water with the potential to produce adverse health effects. Filtering and boiling tap water can lead to changes in the DBP concentrations and modify the exposure through ingestion. Changes in the concentration of 4 individual trihalomethanes (THM4 (chloroform (TCM, bromodichloromethane (BDCM, dibromochloromethane (DBCM, and bromoform (TBM, MX, and bromate were tested when boiling and filtering high bromine-containing tap water from Barcelona. For filtering, we used a pitcher-type filter and a household reverse osmosis filter; for boiling, an electric kettle, a saucepan, and a microwave were used. Samples were taken before and after each treatment to determine the change in the DBP concentration. pH, conductivity, and free/total chlorine were also measured. A large decrease of THM4 (from 48% to 97% and MX concentrations was observed for all experiments. Bromine-containing trihalomethanes were mostly eliminated when filtering while chloroform when boiling. There was a large decrease in the concentration of bromate with reverse osmosis, but there was a little effect in the other experiments. These findings suggest that the exposure to THM4 and MX through ingestion is reduced when using these household appliances, while the decrease of bromate is device dependent. This needs to be considered in the exposure assessment of the epidemiological studies.

  7. The effect of different boiling and filtering devices on the concentration of disinfection by-products in tap water.

    Science.gov (United States)

    Carrasco-Turigas, Glòria; Villanueva, Cristina M; Goñi, Fernando; Rantakokko, Panu; Nieuwenhuijsen, Mark J

    2013-01-01

    Disinfection by-products (DBPs) are ubiquitous contaminants in tap drinking water with the potential to produce adverse health effects. Filtering and boiling tap water can lead to changes in the DBP concentrations and modify the exposure through ingestion. Changes in the concentration of 4 individual trihalomethanes (THM4) (chloroform (TCM), bromodichloromethane (BDCM), dibromochloromethane (DBCM), and bromoform (TBM)), MX, and bromate were tested when boiling and filtering high bromine-containing tap water from Barcelona. For filtering, we used a pitcher-type filter and a household reverse osmosis filter; for boiling, an electric kettle, a saucepan, and a microwave were used. Samples were taken before and after each treatment to determine the change in the DBP concentration. pH, conductivity, and free/total chlorine were also measured. A large decrease of THM4 (from 48% to 97%) and MX concentrations was observed for all experiments. Bromine-containing trihalomethanes were mostly eliminated when filtering while chloroform when boiling. There was a large decrease in the concentration of bromate with reverse osmosis, but there was a little effect in the other experiments. These findings suggest that the exposure to THM4 and MX through ingestion is reduced when using these household appliances, while the decrease of bromate is device dependent. This needs to be considered in the exposure assessment of the epidemiological studies.

  8. ERK Oscillation-Dependent Gene Expression Patterns and Deregulation by Stress-Response

    Energy Technology Data Exchange (ETDEWEB)

    Waters, Katrina M.; Cummings, Brian S.; Shankaran, Harish; Scholpa, Natalie E.; Weber, Thomas J.

    2014-09-15

    Studies were undertaken to determine whether ERK oscillations regulate a unique subset of genes in human keratinocytes and subsequently, whether the p38 stress response inhibits ERK oscillations. A DNA microarray identified many genes that were unique to ERK oscillations, and network reconstruction predicted an important role for the mediator complex subunit 1 (MED1) node in mediating ERK oscillation-dependent gene expression. Increased ERK-dependent phosphorylation of MED1 was observed in oscillating cells compared to non-oscillating counterparts as validation. Treatment of keratinocytes with a p38 inhibitor (SB203580) increased ERK oscillation amplitudes and MED1 and phospho-MED1 protein levels. Bromate is a probable human carcinogen that activates p38. Bromate inhibited ERK oscillations in human keratinocytes and JB6 cells and induced an increase in phospho-p38 and decrease in phospho-MED1 protein levels. Treatment of normal rat kidney cells and primary salivary gland epithelial cells with bromate decreased phospho-MED1 levels in a reversible fashion upon treatment with p38 inhibitors (SB202190; SB203580). Our results indicate that oscillatory behavior in the ERK pathway alters homeostatic gene regulation patterns and that the cellular response to perturbation may manifest differently in oscillating vs non-oscillating cells.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2012-10-01

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

  10. Comparison of methylisoborneol and geosmin abatement in surface water by conventional ozonation and an electro-peroxone process.

    Science.gov (United States)

    Yao, Weikun; Qu, Qiangyong; von Gunten, Urs; Chen, Chao; Yu, Gang; Wang, Yujue

    2017-01-01

    In this study methylisoborneol (MIB) and geosmin abatement in a surface water by conventional ozonation and the electro-peroxone (E-peroxone) process was compared. Batch tests with addition of ozone (O3) stock solutions and semi-batch tests with continuous O2/O3 gas sparging (simulating real ozone contactors) were conducted to investigate O3 decomposition, •OH production, MIB and geosmin abatement, and bromate formation during the two processes. Results show that with specific ozone doses typically used in routine drinking water treatment (0.5-1.0 mg O3/mg dissolved organic carbon (DOC)), conventional ozonation could not adequately abate MIB and geosmin in a surface water. While increasing the specific ozone doses (1.0-2.5 mg O3/mg DOC) could enhance MIB and geosmin abatement by conventional ozonation, this approach resulted in significant bromate formation. By installing a carbon-based cathode to electrochemically produce H2O2 from cathodic oxygen reduction, conventional ozonation can be conveniently upgraded to an E-peroxone process. The electro-generated H2O2 considerably enhanced the kinetics and to a lesser extent the yields of hydroxyl radical (•OH) from O3 decomposition. Consequently, during the E-peroxone process, abatement of MIB and geosmin occurred at much higher rates than during conventional ozonation. In addition, for a given specific ozone dose, the MIB and geosmin abatement efficiencies increased moderately in the E-peroxone (by ∼8-9% and ∼10-25% in the batch and semi-batch tests, respectively) with significantly lower bromate formation compared to conventional ozonation. These results suggest that the E-peroxone process may serve as an attractive backup of conventional ozonation processes during accidental spills or seasonal events such as algal blooms when high ozone doses are required to enhance MIB and geosmin abatement. Copyright © 2016 Elsevier Ltd. All rights reserved.

  11. Process analysis and economics of drinking water production from coastal aquifers containing chromophoric dissolved organic matter and bromide using nanofiltration and ozonation.

    Science.gov (United States)

    Sobhani, R; McVicker, R; Spangenberg, C; Rosso, D

    2012-01-01

    In regions characterized by water scarcity, such as coastal Southern California, groundwater containing chromophoric dissolved organic matter is a viable source of water supply. In the coastal aquifer of Orange County in California, seawater intrusion driven by coastal groundwater pumping increased the concentration of bromide in extracted groundwater from 0.4 mg l⁻¹ in 2000 to over 0.8 mg l⁻¹ in 2004. Bromide, a precursor to bromate formation is regulated by USEPA and the California Department of Health as a potential carcinogen and therefore must be reduced to a level below 10 μg l⁻¹. This paper compares two processes for treatment of highly coloured groundwater: nanofiltration and ozone injection coupled with biologically activated carbon. The requirement for bromate removal decreased the water production in the ozonation process to compensate for increased maintenance requirements, and required the adoption of catalytic carbon with associated increase in capital and operating costs per unit volume. However, due to the absence of oxidant addition in nanofiltration processes, this process is not affected by bromide. We performed a process analysis and a comparative economic analysis of capital and operating costs for both technologies. Our results show that for the case studied in coastal Southern California, nanofiltration has higher throughput and lower specific capital and operating cost, when compared to ozone injection with biologically activate carbon. Ozone injection with biologically activated carbon, compared to nanofiltration, has 14% higher capital cost and 12% higher operating costs per unit water produced while operating at the initial throughput. Due to reduced ozone concentration required to accommodate for bromate reduction, the ozonation process throughput is reduced and the actual cost increase (per unit water produced) is 68% higher for capital cost and 30% higher for operations. Copyright © 2011 Elsevier Ltd. All rights reserved.

  12. Determination of Thiocyanate by Kinetic Spectrophotometric Flow Injection Analysis

    Directory of Open Access Journals (Sweden)

    Mohsen Keyvanfard

    2013-01-01

    Full Text Available A simple and rapid flow injection spectrophotometric method has been developed for the determination of amount of thiocyanate in wastewaters and well water samples. It is based on the reaction of thiocyanate in hydrochloric acid with janus green and bromate. Reaction was monitored spectrophotometrically by measuring janus green absorbance at λmax=554 nm. The calibration graph was linear over the range 0.02–1.0 μg mL−1 and the detection limit was 0.016 μg mL−1 (s/n=3. The throughput was 25 samples per hour.

  13. Effect of Position and Number of Hydroxyl Groups on the Oscillatory Behaviour of Isomers of Hydroxybenzoic Acid

    Directory of Open Access Journals (Sweden)

    Masood A. Nath

    2009-01-01

    Full Text Available In the present communication, the effect of isomers of hydroxybenzoic acids with respect to their oscillatory behaviour as organic substrates with inorganic bromate and manganese(II ion as catalyst in aqueous acid medium (1.0 M H2SO4 have been studied. The number and the relative position of hydroxyl groups (-OH in the aromatic ring is found to influence the oscillatory behaviour. Besides, the role of bromination reaction and the formation of corresponding bromoderivative is found to be an important step. The experimental findings are within the purview of Field, Koros and Noyes (FKN mechanism.

  14. Renal deterioration caused by carcinogens as a consequence of free radical mediated tissue damage: a review of the protective action of melatonin

    Energy Technology Data Exchange (ETDEWEB)

    Gultekin, Fatih; Hicyilmaz, Hicran [Suleyman Demirel University, School of Medicine, Department of Biochemistry, Isparta (Turkey)

    2007-10-15

    This brief review summarizes some of the publications that document the preventive role of melatonin in kidney damage caused by carcinogens such as 2-nitropropane, arsenic, carbon tetrachloride, nitrilotriacetic acid and potassium bromate. Numerous chemicals generate excessive free radicals that eventually induce renal worsening. Melatonin partially or totally prevents free radical mediated tissue damages induced by many carcinogens. Protective actions of melatonin against the harmful effects of carcinogens are believed to stem from its direct free radical scavenging and indirect antioxidant activities. Dietary or pharmacologically given melatonin may attenuate the oxidative stress, thereby mitigating the subsequent renal damage. (orig.)

  15. Spectrophotometric determination of nitrite by its catalytic effect on ...

    African Journals Online (AJOL)

    Under the optimum experimental conditions (sulfuric acid, 0.3 M; CR, 0.75x10-4 M; potassium bromate, 5x10-4 M and 25 oC), nitrite can be determined in the range of 0.015–0.75 µg mL−1 with the detection limit of 0.006 µg mL−1. The relative standard deviation of five replicate determination of 0.25 µg mL−1 nitrite was ...

  16. A Pendulum-Like Motion of Nanofiber Gel Actuator Synchronized with External Periodic pH Oscillation

    Directory of Open Access Journals (Sweden)

    Shuji Hasimoto

    2011-02-01

    Full Text Available In this study, we succeeded in manufacturing a novel nanofiber hydrogel actuator that caused a bending and stretching motion synchronized with external pH oscillation, based on a bromate/sulfite/ferrocyanide reaction. The novel nanofiber gel actuator was composed of electrospun nanofibers synthesized by copolymerizing acrylic acid and hydrophobic butyl methacrylate as a solubility control site. By changing the electrospinning flow rate, the nanofiber gel actuator introduced an anisotropic internal structure into the gel. Therefore, the unsymmetrical motion of the nanofiber actuator was generated.

  17. Oscillatory behaviour of isomers of hydroxybenzoic acid with and without catalyst

    Energy Technology Data Exchange (ETDEWEB)

    Nath, Masood A.; Rastogi, R.P.; Peerzada, G.M. [University of Kashmir, Srinagar (India). Dept. of Chemistry]. E-mail: nath_masood@yahoo.co.in

    2009-07-01

    The present work establishes and compares the oscillatory behaviour of mono-, di- and trihydroxybenzoic acids as organic substrates in acidic bromate (1.0 mol L{sup -1} H{sub 2}SO{sub 4}) without catalyst and in the presence of Mn{sup 2+} ion as the main catalyst. The oscillations are also affected by other catalyst such as Fe{sup 2+} ion. Further, the oscillations start diminishing in mixed catalyst systems. The experimental parameters were obtained potentiometrically and the results have been interpreted on the basis of FKN mechanism. (author)

  18. Ozone and hydrogen peroxide applications for disinfection by-products control in drinking water; Applicazioni con ozono e perossido di idrogeno per il controllo dei sottoprodotti di disinfezione nelle acque potabili

    Energy Technology Data Exchange (ETDEWEB)

    Collivignarelli, C.; Sorlini, S. [Brescia Univ., Brescia (Italy). Dipt. di Ingegneria Civile; Colombino, M. [Azienda Mediterranea Gas e Acqua, Genoa (Italy); Riganti, V. [Pavia Univ., Pavia (Italy). Dipt. di Chimica Generale

    2001-04-01

    A great interest has been developed during the last years for ozone in drinking water treatments thanks to its strong oxidant and disinfectant power and for its efficiency in disinfection by-products (DBPs) precursors removal. However ozonization produces some specific DBPs, such as aldehydes and ketones; moreover, the presence of bromide in raw water engages ozone in a complex cycle in which both organic bromide and inorganic bromate are end products. In this paper the combination of hydrogen peroxide with ozone (known as peroxone process) and the ozone alone process were experimented on one surface water coming from the lake of Brugneto (Genova) in order to investigate bromate formation and trihalomethanes precursors removal during the oxidation process. The results show that the advanced peroxone process can be applied for bromate reduction (about 30-40%) with better results in comparison with the ozone alone process, while no advantages are shown for THMs precursors removal. The addition of in-line filtration step after pre-oxidation improves both bromate and THMs precursors removal, particularly with increasing hydrogen peroxide/ozone ratio in the oxidation step. [Italian] Un notevole interesse e' stato mostrato di recente per l'utilizzo dell'ozono nei trattamenti di potabilizzazione sia per il suo forte potere ossidante e disinfettante sia per la capacita' di rimuovere alcuni precursori di formazione dei sottoprodotti di ossidazione (OBPs). Tuttavia, anche l'ozono puo' produrre a sua volta alcuni specifici sottoprodotti, quali aldeidi e chetoni; inoltre, la presenza di bromuro nell'acqua grezza coinvolge l'ozono in una serie di reazioni che portano alla formazione di composti organici bromurati e di sottoprodotti inorganici, i piu' noti tra i quali sono i bromati. In questo articolo vengono presentati i risultati di alcuni trattamenti di ossidazione convenzionali a base di ozono combinato con perossido di idrogeno

  19. Application of methyl orange oxidation in the presence of hydrazine to kinetic determination of periodate ion

    OpenAIRE

    Danilina, E.; Ibragimova, Yu

    2014-01-01

    It is possible to apply the induction period of Landolt reaction of methyl orange with potassium bromate in the presence of hydrazine to determination of periodate ion. Optimal conditions are: 0.030 M HCl, 10 mg/mL methyl orange, 1.6·10 -4 M KBrO 3, 3·10-5 M N 2H 4. Calibration curve is linear (0.06-0.9) mg/mL periodate ion range, reproducibility error is 2.6%, relative error is 4.6%.

  20. Mineralizing urban net-zero water treatment: Phase II field ...

    Science.gov (United States)

    Net-zero water (NZW) systems, or water management systems achieving high recycling rates and low residuals generation so as to avoid water import and export, can also conserve energy used to heat and convey water, while economically restoring local eco-hydrology. However, design and operating experience are extremely limited. The objective of this paper is to present the results of the second phase of operation of an advanced oxidation-based NZW pilot system designed, constructed, and operated for a period of two years, serving an occupied four-person apartment. System water was monitored, either continuously or thrice daily, for routine water quality parameters, minerals, and MicroTox® in-vitro toxicity, and intermittently for somatic and male-specific coliphage, adenovirus, Cryptosporidium, Giardia, emerging organic constituents (non-quantitative), and the Florida drinking water standards. All 115 drinking water standards with the exception of bromate were met in this phase. Neither virus nor protozoa were detected in the treated water, with the exception of measurement of adenovirus genome copies attributed to accumulation of inactive genetic material in hydraulic dead zones. Chemical oxygen demand was mineralized to 90% in treatment. Total dissolved solids were maintained at ∼500 mg/L at steady state, partially through aerated aluminum electrocoagulation. Bromate accumulation is projected to be controlled by aluminum electrocoagulation with separate dispo

  1. Optimized removal of dissolved organic carbon and trace organic contaminants during combined ozonation and artificial groundwater recharge.

    Science.gov (United States)

    Hübner, U; Miehe, U; Jekel, M

    2012-11-15

    Pilot scale experiments using an 8 g/h ozonation unit and a 1.4 m(2) slow sand filter have demonstrated that the combination of ozonation and artificial groundwater recharge is suitable for efficient reduction of bulk and trace organics. The biodegradation of dissolved organic carbon (DOC) in the slow sand filter was enhanced from 22% without pre-treatment to 34% by pre-ozonation. In addition, realistic surface water concentrations of most investigated trace organic compounds (TrOCs) including carbamazepine, sulfamethoxazole, phenazone and metoprolol were reduced below the limits of quantification. Only a few TrOCs, e.g. primidone and benzotriazole, were not efficiently removed in both treatment steps and could be detected regularly in the filter effluent. For these compounds, enhanced treatment, such as advanced oxidation processes, needs to be considered. Testing for genotoxicity and cytotoxicity did not reveal any systematic adverse effects for human health. The formation of the by-product bromate from bromide was below the limit of the German drinking water directive of 10 μg/L. No removal of bromate was observed in the aerobic slow sand filter. Additional experiments with sand columns showed that operating a preceding bank filtration step to reduce DOC can reduce oxidant demand by approximately 20%. Copyright © 2012 Elsevier Ltd. All rights reserved.

  2. Kinetic spectrophotometric determination of trace amounts of selenium and vanadium

    Energy Technology Data Exchange (ETDEWEB)

    Safavi, A.; Sedghy, H.R.; Shams, E. [Dept. of Chemistry, Shiraz Univ. (Iran)

    1999-11-01

    A sensitive kinetic spectrophotometric method has been developed for the determination of Se(IV) over the range of 45 to 4000 ng in 10 mL of solution. The method is based on the catalytic effect of Se(IV) on the reduction reaction of bromate by hydrazinium dichloride, with subsequent reaction of Ponceau S with products of the above reaction (chlorine and bromine), causing color changing of Ponceau S. Method development includes optimization of time interval for measurement of slope, pH, reagents concentration, and temperature. The optimized conditions yielded a theoretical detection limit of 33 ng/10 mL of solution of Se(IV). The interfering effects were studied and removed. The method was applied to the determination of selenium in spiked water, Kjeldahl tablet, selenium tablet, and shampoo. Vanadium(V) has an inhibition effect on the catalyzed reaction of bromate and hydrazine by selenium. Using this effect, V(V) can be determined in the range of 70 to 2500 ng in 10 mL of solution. The optimization procedure includes pH and selenium concentration. An extraction method was used for interference removal. The method was applied to the determination of vanadium in petroleum. (orig.)

  3. Second-order advantage from kinetic-spectroscopic data matrices in the presence of extreme spectral overlapping

    Energy Technology Data Exchange (ETDEWEB)

    Culzoni, Maria J. [Laboratorio de Desarrollo Analitico y Quimiometria (LADAQ), Catedra de Quimica Analitica I, Facultad de Bioquimica y Ciencias Biologicas, Universidad Nacional del Litoral, Ciudad Universitaria, Santa Fe S3000ZAA (Argentina); Goicoechea, Hector C. [Laboratorio de Desarrollo Analitico y Quimiometria (LADAQ), Catedra de Quimica Analitica I, Facultad de Bioquimica y Ciencias Biologicas, Universidad Nacional del Litoral, Ciudad Universitaria, Santa Fe S3000ZAA (Argentina)], E-mail: hgoico@fbcb.unl.edu.ar; Ibanez, Gabriela A.; Lozano, Valeria A. [Departamento de Quimica Analitica, Facultad de Ciencias Bioquimicas y Farmaceuticas, Universidad Nacional de Rosario and Instituto de Quimica Rosario (IQUIR-CONICET), Suipacha 531, Rosario S2002LRK (Argentina); Marsili, Nilda R. [Laboratorio de Desarrollo Analitico y Quimiometria (LADAQ), Catedra de Quimica Analitica I, Facultad de Bioquimica y Ciencias Biologicas, Universidad Nacional del Litoral, Ciudad Universitaria, Santa Fe S3000ZAA (Argentina); Olivieri, Alejandro C. [Departamento de Quimica Analitica, Facultad de Ciencias Bioquimicas y Farmaceuticas, Universidad Nacional de Rosario and Instituto de Quimica Rosario (IQUIR-CONICET), Suipacha 531, Rosario S2002LRK (Argentina)], E-mail: aolivier@fbioyf.unr.edu.ar; Pagani, Ariana P. [Departamento de Quimica Analitica, Facultad de Ciencias Bioquimicas y Farmaceuticas, Universidad Nacional de Rosario and Instituto de Quimica Rosario (IQUIR-CONICET), Suipacha 531, Rosario S2002LRK (Argentina)

    2008-04-28

    Multivariate curve resolution coupled to alternating least-squares (MCR-ALS) has been employed to model kinetic-spectroscopic second-order data, with focus on the achievement of the important second-order advantage, under conditions of extreme spectral overlapping among sample components. A series of simulated examples shows that MCR-ALS can conveniently handle the studied analytical problem unlike other second-order multivariate calibration algorithms, provided matrix augmentation is implemented in the spectral mode instead of in the usual kinetic mode. The approach has also been applied to three experimental examples, which involve the determination of: (1) the antiparkinsonian carbidopa (analyte) in the presence of levodopa as a potential interferent, both reacting with cerium (IV) to produce the fluorescent species cerium (III) with different kinetics; (2) Fe(II) (analyte) in the presence of the interferent Zn(II), both catalyzing the oxidation of methyl orange with potassium bromate; and (3) tartrazine (analyte) in the presence of the interferent brilliant blue, both oxidized with potassium bromate, with the interferent leading to a product with an absorption spectrum very similar to tartrazine. The results indicate good analytical performance towards the analytes, despite the intense spectral overlapping and the presence of unexpected constituents in the test samples.

  4. Occurrence and Assessment of Chemical Contaminants in Drinking Water in Tunceli, Turkey

    Directory of Open Access Journals (Sweden)

    Veysel Demir

    2013-01-01

    Full Text Available The objective of this study was to analyze drinking water samples from 21 sites in the city center and seven municipalities of Tunceli, Turkey, in order to determine the presence of nitrate, nitrite, fluoride, bromate, pesticides, polycyclic aromatic hydrocarbons (PAHs, trihalomethanes (THMs, and some other chemicals. In all locations, the concentrations of chemicals investigated were below the permissible limits set by local and international organizations for drinking water. Low levels of nitrate (4.79 ± 4.20 mg/L, fluoride (0.11 ± 0.08 mg/L, and THMs (6.63 ± 5.14 μg/L were detected in all locations. A low level of tetra, chloroethane, which is suspected to be a human carcinogen, was also detected in 8 locations in the range of 0.26–0.43 μg/L. These contaminants may pose adverse health effects or minimum hazard due to long-term exposure. In all locations, bromate, benzene, total PAH, 1-2 dichloroethane, vinyl chloride, acrylamide, and epichloridine levels in drinking water samples were under detection limits.

  5. Influence of the Belousov–Zhabotinsky substrate concentration on the lifetime and self-oscillating behavior of a polymer solution

    Directory of Open Access Journals (Sweden)

    Nakazumi Tomoka

    2017-01-01

    Full Text Available In this study, we synthesized a self-oscillating polymer chain with N-ethylacrylamide (NEAAm as the main-chain. This exhibits a higher lower critical solution temperature than an N-isopropylacrylamide main chain. We subsequently measured the transmittance self-oscillation of poly[NEAAm-co-Ru(bpy3] [Ru(bpy3 = 4-vinyl-4’-methyl-2,2’-bipyridinebis(2,2’ bipyridinebis(hexafluorophosphate ruthenium] solutions comprising three Belousov-Zhabotinsky (BZ substrates (malonic acid, sodium bromate, and sulfuric acid, under stirring at constant temperature. The soluble-insoluble self-oscillation of the polymer solution originated from the different solubility of the Ru(bpy3 moiety as a catalyst of the BZ reaction in the reduced and oxidized states. We demonstrated that the self-oscillating behavior was significantly affected by the initial concentration of the sodium bromate. Moreover, we clarified that the lifetime of the transmittance self-oscillation can be predicted from the initial concentration of malonic acid.

  6. Chiral symmetry breaking in unstirred crystallization

    Energy Technology Data Exchange (ETDEWEB)

    Szurgot, M. [Center of Mathematics and Physics, Technical University of Lodz (Poland)

    2012-01-15

    Statistics of nucleation of chiral forms of sodium bromate from unstirred aqueous solutions was studied. It was established that bimodal, trimodal and unimodal distributions of enantiomers are obtained in unstirred crystallization. It was also found out that probabilities of the creation of L or D crystals and racemates R, as well as the presence of D, L, and R peaks in distributions depend on crystallizer size, supersaturation and temperature. Nucleation at low supersaturations in small, closed crystallizers leads to the formation of pure enantiomers, and to bimodal distributions with D and L peaks at any temperature. At high supersaturations in large, open crystallizers the formation of racemates and unimodal distributions with racemate R peaks results. In open crystallizers at the lowest temperatures and at the highest temperatures used in crystallization from aqueous solution racemates of sodium bromate are preferentially formed, but in a wide range of intermediate-temperatures apart from racemates, pure enantiomers are efficiently formed which leads to trimodal distributions. The spontaneous formation of pure enantiomers in crystallization from unstirred, unseeded solutions is caused by the chiral symmetry breaking phenomenon, the same as that discovered in stirred crystallization. The conservation of chiral symmetry is, in unstirred crystallization, one of the two possibilities, and the other one is the breakage of symmetry. Both of them occur in nature. (copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  7. Trace vanadium analysis by catalytic adsorptive stripping voltammetry using mercury-coated micro-wire and polystyrene-coated bismuth film electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Dansby-Sparks, Royce; Chambers, James Q. [Department of Chemistry, University of Tennessee, Knoxville, TN 37996-1600 (United States); Xue Ziling, E-mail: xue@ion.chem.utk.edu [Department of Chemistry, University of Tennessee, Knoxville, TN 37996-1600 (United States)

    2009-06-08

    An electrochemical technique has been developed for ultra-trace (ng L{sup -1}) vanadium (V) measurement. Catalytic adsorptive stripping voltammetry for V analysis was developed at mercury-coated gold micro-wire electrodes (MWEs, 100 {mu}m) in the presence of gallic acid (GA) and bromate ion. A potential of -0.275 V (vs Ag/AgCl) was used to accumulate the complex in acetate buffer (pH 5.0) at the electrode surface followed by a differential pulse voltammetric scan. Parameters affecting the electrochemical response, including pH, concentration of GA and bromate, deposition potential and time have been optimized. Linear response was obtained in the 0-1000 ng L{sup -1} range (2 min deposition), with a detection limit of 0.88 ng L{sup -1}. The method was validated by comparison of results for an unknown solution of V by atomic absorption measurement. The protocol was evaluated in a real sample by measuring the amount of V in river water samples. Thick bismuth film electrodes with protective polystyrene films have also been made and evaluated as a mercury free alternative. However, ng L{sup -1} level detection was only attainable with extended (10 min) deposition times. The proposed use of MWEs for the detection of V is sensitive enough for future use to test V concentration in biological fluids treated by the advanced oxidation process (AOP).

  8. Easy to use program “Simkine3” for simulating kinetic profiles of multi-step chemical Systems and optimisation of predictable rate coefficients therein

    Directory of Open Access Journals (Sweden)

    S.B. Jonnalagadda

    2012-08-01

    Full Text Available ‘Simkine3’, a Delphi based software is developed to simulate the kinetic schemes of complex reaction mechanisms involving multiple sequential and competitive elementary steps for homogeneous and heterogeneous chemical reactions. Simkine3 is designed to translate the user specified mechanism into chemical first-order differential equations (ODEs and optimise the estimated rate constants in such a way that simulated curves match the experimental kinetic profiles. TLSoda which uses backward differentiation method is utilised to solve resulting ODEs and Downhill Simplex method is used to optimise the estimated rate constants in a robotic way. An online help file is developed using HelpScrible Demo to guide the users of Simkine3. The versatility of the software is demonstrated by simulating the complex reaction between methylene violet and acidic bromate, a reaction which exhibits complex nonlinear kinetics. The new software is validated after testing it on a 19-step intricate mechanism involving 15 different species. The kinetic profiles of multiple simulated curves, illustrating the effect of initial concentrations of bromate, and bromide were matched with the corresponding experimental curves.DOI: http://dx.doi.org/10.4314/bcse.v26i2.10

  9. Semiconductor-mediated photocatalysed degradation of two selected azo dye derivatives, amaranth and bismarck brown in aqueous suspension.

    Science.gov (United States)

    Tariq, M Abu; Faisal, M; Muneer, M

    2005-12-09

    Semiconductor-mediated photocatalysed degradation of two selected azo dye derivatives such as amaranth (1) and bismarck brown (2) has been investigated in aqueous suspension by monitoring the change in substrate concentration employing UV spectroscopic analysis technique as a function of irradiation time. The degradation was studied under different conditions such as types of TiO(2), pH, substrate concentration, catalyst concentration, and in the presence of electron acceptors such as hydrogen peroxide (H(2)O(2)), potassium bromate (KBrO(3)) and ammonium persulphate (NH(4))(2)S(2)O(8) besides air. The degradation rates were found to be strongly influenced by all the above parameters. The photocatalyst Degussa P25 showed comparatively highest photocatalytic activity. The dye derivative, bismarck brown (2) was found to degrade faster than amaranth dye (1).

  10. Kinetic spectrophotometric method for the determination of morphine in biological samples

    Science.gov (United States)

    Sheibani, A.; Shishehbore, M. Reza; Mirparizi, E.

    2010-10-01

    In this paper a simple, selective and inexpensive kinetic method was developed for the determination of morphine based on its inhibitory effect on the Janus green-bromate system in sulfuric acid media. The reaction was monitored spectrophotometrically at 618 nm by a fixed time method. The effect of different parameters such as concentration of reactants and temperature on the rate of reaction was investigated and optimum conditions were obtained. The calibration curve was linear in the concentration range 0.07-7.98 mg L -1 of morphine, and detection limit of the method was 3.0 × 10 -2 mg L -1. The relative standard deviation for five determinations of 3.74 mg L -1 of morphine was 0.57%. Finally, the proposed method was successfully applied to the determination of morphine in human urine and serum as real samples.

  11. Carbon-dot-based dual-emission silica nanoparticles as a ratiometric fluorescent probe for Bisphenol A

    Science.gov (United States)

    Xiang, Guo-Qiang; Ren, Yue; Xia, Yin; Mao, Wenjie; Fan, Chao; Guo, Si-Yu; Wang, Pan-Pan; Yang, Deng-Hui; He, Lijun; Jiang, Xiuming

    2017-04-01

    A simple and effective strategy for designing a ratiometric fluorescent nanosensor is described in this work. A carbon dots (CDs) based dual-emission nanosensor for Bisphenol A (BPA) was prepared by coating CDs on the surface of dye-doped silica nanoparticles. The fluorescence of dual-emission silica nanoparticles was quenched in hydrochloric acid by potassium bromate (KBrO3) oxidation; BPA inhibited KBrO3 oxidation, resulting in the ratiometric fluorescence response of dual-emission silica nanoparticles. Several important parameters affecting the performance of the nanosensor were investigated and optimized. The detection limit of this nanosensor was 0.80 ng mL- 1 with a linear range from 10 to 500 ng mL- 1. This was applied successfully to determine BPA in the leached solution of different plastic products with satisfactory results.

  12. A fixed cations and low Tg polymer: the poly(4-vinyl-pyridine) quaternized by poly(ethylene oxide) links. Conductivity study; Un electrolyte polymere a cations fixes et bas Tg: les poly(4-vinylpyridine) quaternisees par des chainons de poly(oxyde d`ethylene). Etude de la conductivite

    Energy Technology Data Exchange (ETDEWEB)

    Gramain, Ph. [Ecole Nationale Superieure de Chimie de Montpellier, 34 (France); Frere, Y. [Centre National de la Recherche Scientifique (CNRS), 67 - Strasbourg (France). Institut Charles Sadron

    1996-12-31

    The spontaneous ionic polymerization of 4-vinyl-pyridine in presence of mono-tosylated or bromated short chains of poly(ethylene oxide)-(PEO) is used to prepare amorphous comb-like poly-cations with low Tg. The polymer electrolyte properties of these new structures have been studied without any addition of salts. The ionic conductivity of these fixed cation poly-electrolytes depends on the length of the grafted PEO and varies from 10{sup -7} to 10{sup -4} S/cm between 25 and 80 deg. C. It is only weakly dependent on the nature of the cation but it is controlled by the movements of the pyridinium cation which are facilitated by the plastifying effect of the POE chains which do not directly participate to the ionic transport. (J.S.) 17 refs.

  13. Copper(I) Bromide: An Alternative Emitter for Blue-Colored Flame Pyrotechnics.

    Science.gov (United States)

    Juknelevicius, Dominykas; Karvinen, Eero; Klapötke, Thomas M; Kubilius, Rytis; Ramanavicius, Arunas; Rusan, Magdalena

    2015-10-19

    Copper(I) bromide was evaluated as an alternative emitter for blue flame pyrotechnic compositions. CuBr and CuCl emission spectra were recorded from a butane torch flame and compared. Cu(BrO3 )2 was synthesized and used in pyrotechnic compositions as an oxidizer and the source for the generation of CuBr species. Pyrotechnic compositions, which contained copper and potassium bromates as oxidizers, were optimized for the generation of blue flames. The experimental data, including emission spectra of the flames, chromaticity coordinates, burning rates, luminous intensities, and sensitivity tests, were analyzed and compared. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  14. PIXE analysis of Nigerian flour and bread samples

    Science.gov (United States)

    Olise, Felix S.; Fernandes, Adriana M.; Cristina Chaves, P.; Taborda, Ana; Reis, Miguel A.

    2014-01-01

    The alleged use of potassium bromate (KBrO3) in bread baking led a few authors to report on the chemical methods for the determination of KBrO3 levels in bread. In order to examine the potentials of a non chemical particle induced X-ray emission (PIXE) method for this purpose, six sets of samples, each composed of flour, dough and bread from a production batch were analysed. The samples were obtained from six different bakers of bread at Ile-Ife, Nigeria. The flour samples were air-dried while others were freeze dried at about -16 °C. The samples were homogenised in an agate mortar and then pelletised. Samples were analysed at the CTN standard PIXE setup and standard procedures for thick target samples analysis were followed. In some samples significant concentrations of bromine were found. In the present work we present possible explanations for the presence of this potentially dangerous contaminant in the samples.

  15. The effect of flow rate on the oscillatory activation energy of an oscillating reaction

    Science.gov (United States)

    Monteiro, Emily V.; Varela, Hamilton; Faria, Roberto B.

    2017-09-01

    The simultaneous influence of temperature and flow rate (k0) in the oscillatory regime of the bromate-oxalic acid-acetone-Ce(III) oscillating reaction was investigated. The influence of temperature was evaluated in terms of the oscillatory activation energy (Eω), which was determined at different flow rates. Increasing k0, the oscillatory activation energy is decreased, tending to a limit value, Eω∞. The sensitivity of Eω with k0 is described by the parameter η = dEω/d(1/k0). Eω∞ and η are global properties of any particular oscillating reaction and describes a correlation between the dynamical behavior and temperature, and should be used when comparing different oscillating reactions.

  16. Association between age and repair of oxidatively damaged DNA in human peripheral blood mononuclear cells

    DEFF Research Database (Denmark)

    Løhr, Mille; Jensen, Annie; Eriksen, Louise

    2015-01-01

    It has been hypothesised that positive associations between age and levels of oxidative stress-generated damage to DNA may be related to an age-dependent decline in DNA repair activity. The objective of this study was to investigate the association between age and repair activity of oxidatively......, the results show an inverse association between age and DNA repair activity of oxidatively damaged DNA....... damaged DNA in peripheral blood mononuclear cells (PBMCs). We isolated PBMCs from subjects aged 18-83 years, as part of a health survey of the Danish population that focussed on lifestyle factors. The level of DNA repair activity was measured as incisions on potassium bromate-damaged DNA by the comet...

  17. Photoassisted Degradation of a Herbicide Derivative, Dinoseb, in Aqueous Suspension of Titania

    Directory of Open Access Journals (Sweden)

    Niyaz A. Mir

    2012-01-01

    Full Text Available The titanium dioxide (TiO2 photoassisted degradation of herbicide dinoseb has been examined in aqueous suspensions under UV light irradiation. The degradation kinetics were studied under various conditions such as substrate concentration, type of catalyst, catalyst dosage, pH, and light intensity as well as in presence of electron acceptors such as hydrogen peroxide, potassium bromate, and potassium persulphate under continuous air purging, and the degradation rates were found to be strongly influenced by these parameters. The Degussa P25 was found to be more efficient photocatalyst as compared to other photocatalysts tested. Dinoseb was found to degrade efficiently in acidic pH and all the electron acceptors studied enhanced the degradation rate. The results manifested that the photocatalysis of dinoseb followed pseudo-first-order kinetics. A qualitative study of the degradation products generated during the process was performed by GC-MS, and a degradation mechanism was proposed.

  18. A New Inhibition Kinetic Spectrophotometric Method for the Determination of Resorcinol

    Directory of Open Access Journals (Sweden)

    Mohsen Keyvanfard

    2010-01-01

    Full Text Available A new, simple, inexpensive and fast kinetic spectrophotometric method was developed for the determination of trace amounts of resorcinol over the range of 0.02-0.80 μg/mL. The method is based on the inhibitory effect of resorcinol on the formaldehyde catalyzed oxidation reaction of of cresyl violet by bromate in acidic media is reported. The reaction was monitored spectrophotometrically by measuring the decrease in absorbance of cresyl violet at 596 nm with a fixed-time 0.5–2.5 min from initiation of the reaction.The detection limit is 0.017 μg/mL and relative standard deviation of 0.1 and 0.5 μg/mL resorcinol for six replicate measurements was 2.6 and 2.9 %, respectively. The method was applied to the determination of resorcinol in water samples.

  19. Heterogeneous photocatalyzed degradation of uracil and 5-bromouracil in aqueous suspensions of titanium dioxide

    Energy Technology Data Exchange (ETDEWEB)

    Singh, H.K. [Department of Chemistry, Aligarh Muslim University, Aligarh 202002 (India); Saquib, M. [Department of Chemistry, Aligarh Muslim University, Aligarh 202002 (India); Haque, M.M. [Department of Chemistry, Aligarh Muslim University, Aligarh 202002 (India); Muneer, M. [Department of Chemistry, Aligarh Muslim University, Aligarh 202002 (India)]. E-mail: mmuneer@uclan.ac.uk

    2007-04-02

    Photocatalyzed degradation of uracil (1) and 5-bromouracil (2) has been investigated in aqueous suspensions of titanium dioxide under a variety of conditions. The degradation was studied by monitoring the change in substrate concentration employing UV spectroscopic analysis technique and depletion in total organic carbon (TOC) content as a function of irradiation time. The degradation of the compounds under investigation was studied using various parameters such as, different types of TiO{sub 2} powders, pH, catalyst concentration, substrate concentrations, and in the presence of electron acceptors like hydrogen peroxide (H{sub 2}O{sub 2}) and potassium bromate (KBrO{sub 3}) besides molecular oxygen. Photocatalyst Degussa P25 was found to be more efficient for the degradation of both compounds as compared with other TiO{sub 2} powders such as UV100, PC500 and TTP.

  20. Experimental Evidence of Large Amplitude pH Mediated Autonomous Chemomechanical Oscillation

    Directory of Open Access Journals (Sweden)

    Xin Yang

    2017-10-01

    Full Text Available Large amplitude autonomous chemomechanical oscillations were observed in a coupled system consisting of a porous pH-responsive hydrogel and a bromate-sulfite-manganese (II pH oscillatory reaction. The porous structure effectively improves the chemomechanical response speed, and the negative feedback species of the bulk oscillation Mn2+ takes part in the coupling by forming complex and physical crosslinks with the responsive group in the gel. It strengthens the porous gel by forming additional networks, which may contribute to sustaining the long-lasting chemomechanical oscillation. Additionally, the interaction between Mn2+ and the hydrogel alters the period of the oscillatory reaction due to its binding competition with H+, the positive feedback species.

  1. A New Technique for Quantitative Determination of Dexamethasone in Pharmaceutical and Biological Samples Using Kinetic Spectrophotometric Method

    Directory of Open Access Journals (Sweden)

    Ali Mohammad Akhoundi-Khalafi

    2015-01-01

    Full Text Available Dexamethasone is a type of steroidal medications that is prescribed in many cases. In this study, a new reaction system using kinetic spectrophotometric method for quantitative determination of dexamethasone is proposed. The method is based on the catalytic effect of dexamethasone on the oxidation of Orange G by bromate in acidic media. The change in absorbance as a criterion of the oxidation reaction progress was followed spectrophotometrically. To obtain the maximum sensitivity, the effective reaction variables were optimized. Under optimized experimental conditions, calibration graph was linear over the range 0.2–54.0 mg L−1. The calculated detection limit (3sb/m was 0.14 mg L−1 for six replicate determinations of blank signal. The interfering effect of various species was also investigated. The present method was successfully applied for the determination of dexamethasone in pharmaceutical and biological samples satisfactorily.

  2. Analysis of self-oscillating behaviors aimed at the development of a molecular robot with organic acids as fuel

    Science.gov (United States)

    Nakazumi, Tomoka; Hara, Yusuke

    2017-09-01

    We studied the transmittance self-oscillation of a polymer chain driven by an organic acid as the fuel. The self-oscillating polymer chain consists of 4-acryloylmorpholine (ACMO) and the Ru catalyst (Ru(bpy)3) of the Belousov–Zhabotinsky (BZ) reaction. The transmittance self-oscillating behavior was affected significantly by the temperature. As the amplitude of the transmittance self-oscillation, which is reflected by the aggregation state, decreased with time, the oscillation period also decreased. This trend indicates that the polymer aggregation affects the rate of the BZ reaction significantly. The activation energy of the self-oscillating value was almost the same in the normal BZ reaction, which does not include Ru(bpy)3 complexes in the polymer chains. In addition, we demonstrated the effect of one BZ substrate (sodium bromate or malonic acid) on the transmittance self-oscillation period.

  3. Preparation and electrocatalytic application of composites containing gold nanoparticles protected with rhodium-substituted polyoxometalates

    Energy Technology Data Exchange (ETDEWEB)

    Wiaderek, Kamila M. [Department of Chemistry and Biochemistry, Miami University, Oxford, OH 45056 (United States); Cox, James A., E-mail: coxja@muohio.ed [Department of Chemistry and Biochemistry, Miami University, Oxford, OH 45056 (United States)

    2011-04-01

    Substitution of a metal center of phosphomolybdate, PMo{sub 12}O{sub 40}{sup 3-} (PMo{sub 12}), or its tungsten analogue with dirhodium(II) and subsequent stabilization of gold nanoparticles, AuNPs, with Rh{sub 2}PMo{sub 11} are demonstrated. The AuNP-Rh{sub 2}PMo{sub 11} mediates oxidations but adsorbs too weakly for direct modification of electrode materials. Stability in quiescent solution was achieved by modifying glassy carbon (GC) with 3-aminopropyltriethoxysilane (APTES) and then electrostatically assembling AuNP-Rh{sub 2}PMo{sub 11}. At GC|APTES|AuNP-Rh{sub 2}PMo{sub 11}, cyclic voltammetry showed the expected set of three reversible peak-pairs for PMo{sub 11} in the range -0.2 to 0.6 vs. (Ag/AgCl)/V and the reversible Rh{sup II,III} couple at 1.0 vs. (Ag/AgCl)/V. The presence of AuNPs increased the current for the reduction of bromate by a factor of 2.5 relative to that at GC|Rh{sub 2}PMo{sub 11}, and the electrocatalytic oxidation of methionine displayed characteristics of synergism between the AuNP and Rh{sup II}. To stabilize AuNP-Rh{sub 2}PMo{sub 11} on a surface in a flow system, GC was modified by electrochemically assisted deposition of a sol-gel with templated 10-nm pores prior to immobilizing the catalyst in the pores. The resulting electrode permitted determination of bromate by flow-injection amperometry with a detection limit of 4.0 x 10{sup -8} mol dm{sup -3}.

  4. Induction and repair of DNA damage measured by the comet assay in human T lymphocytes separated by immunomagnetic cell sorting.

    Science.gov (United States)

    Bausinger, Julia; Speit, Günter

    2014-11-01

    The comet assay is widely used in human biomonitoring to measure DNA damage in whole blood or isolated peripheral blood mononuclear cells (PBMC) as a marker of exposure to genotoxic agents. Cytogenetic assays with phytohemagglutinin (PHA)-stimulated cultured T lymphocytes are also frequently performed in human biomonitoring. Cytogenetic effects (micronuclei, chromosome aberrations, sister chromatid exchanges) may be induced in vivo but also occur ex vivo during the cultivation of lymphocytes as a consequence of DNA damage present in lymphocytes at the time of sampling. To better understand whether DNA damage measured by the comet assay in PBMC is representative for DNA damage in T cells, we comparatively investigated DNA damage and its repair in PBMC and T cells obtained by immunomagnetic cell sorting. PBMC cultures and T cell cultures were exposed to mutagens with different modes of genotoxic action and DNA damage was measured by the comet assay after the end of a 2h exposure and after 18h post-incubation. The mutagens tested were methyl methanesulfonate (MMS), (±)-anti-B[a]P-7,8-dihydrodiol-9,10-epoxide (BPDE), 4-nitroquinoline-1-oxide (4NQO), styrene oxide and potassium bromate. MMS and potassium bromate were also tested by the modified comet assay with formamido pyrimidine glycosylase (FPG) protein. The results indicate that the mutagens tested induce DNA damage in PBMC and T cells in the same range of concentrations and removal of induced DNA lesions occurs to a comparable extent. Based on these results, we conclude that the comet assay with PBMC is suited to predict DNA damage and its removal in T cells. Copyright © 2014 Elsevier B.V. All rights reserved.

  5. UTILIZATION OF BROMINATION REACTION FOR THE SPECTROPHOTOMETRIC ASSAY OF DOMPERIDONE IN PHARMACEUTICALS

    Directory of Open Access Journals (Sweden)

    O. ZENITA DEVI

    2011-03-01

    Full Text Available Three simple and sensitive spectrophotometric methods are described for the determination of domperidone (DOM in bulk drug and in dosage forms using bromate-bromide mixture as brominating agent in acid medium and three dyes, meta-cresol purple (MCP, amaranth (AMR and erioglaucine (EGC. The methods involve the addition of a known excess of bromate-bromide mixture to an acidified solution of DOM followed by the determination of the residual bromine by reacting with a fixed amount of either MCP dye and measuring the absorbance at 530 nm (method A or AMR dye and measuring the absorbance at 520 nm (method B or EGC dye and measuring the absorbance at 630 nm (method C. Beer’s law is obeyed over the concentration ranges, 0.63–10.0, 0.25-4.0 and 0.13-2.0 µg mL-1 for method A, B and C, respectively. The ap¬parent molar absorptivities are calculated to be 3.751x104, 6.604x104 and 1.987x105 L mol-1cm-1 for method A, B and C, respectively, and the corresponding sandell sensitivity values are 0.011, 0.006 and 0.002 μg cm-2. The limit of detection and the limit of quantification are also reported for all the three methods. No interference was observed from common additives found in pharmaceutical preparations. Statistical comparisons of the results with those of the reference method showed excellent agreement, and indicated no significant difference in accuracy and precision. The accuracy and reliability of the methods were further ascertained by performing recovery tests via standardaddition technique.

  6. Advanced oxidation and disinfection processes for onsite net-zero greywater reuse: A review.

    Science.gov (United States)

    Gassie, Lucien W; Englehardt, James D

    2017-11-15

    Net-zero greywater (NZGW) reuse, or nearly closed-loop recycle of greywater for all original uses, can recover both water and its attendant hot-water thermal energy, while avoiding the installation and maintenance of a separate greywater sewer in residential areas. Such a system, if portable, could also provide wash water for remote emergency health care units. However, such greywater reuse engenders human contact with the recycled water, and hence superior treatment. The purpose of this paper is to review processes applicable to the mineralization of organics, including control of oxidative byproducts such as bromate, and maintenance of disinfection consistent with potable reuse guidelines, in NZGW systems. Specifically, TiO2-UV, UV-hydrogen peroxide, hydrogen peroxide-ozone, ozone-UV advanced oxidation processes, and UV, ozone, hydrogen peroxide, filtration, and chlorine disinfection processes were reviewed for performance, energy demand, environmental impact, and operational simplicity. Based on the literature reviewed, peroxone is the most energy-efficient process for organics mineralization. However, in portable applications where delivery of chemicals to the site is a concern, the UV-ozone process appears promising, at higher energy demand. In either case, reverse osmosis, nanofiltration, or ED may be useful in controlling the bromide precursor in make-up water, and a minor side-stream of ozone may be used to prevent microbial regrowth in the treated water. Where energy is not paramount, UV-hydrogen peroxide and UV-TiO2 can be used to mineralize organics while avoiding bromate formation, but may require a secondary process to prevent microbial regrowth. Chlorine and ozone may be useful for maintenance of disinfection residual. Copyright © 2017 Elsevier Ltd. All rights reserved.

  7. Organic Contaminant Abatement in Reclaimed Water by UV/H2O2 and a Combined Process Consisting of O3/H2O2 Followed by UV/H2O2: Prediction of Abatement Efficiency, Energy Consumption, and Byproduct Formation.

    Science.gov (United States)

    Lee, Yunho; Gerrity, Daniel; Lee, Minju; Gamage, Sujanie; Pisarenko, Aleksey; Trenholm, Rebecca A; Canonica, Silvio; Snyder, Shane A; von Gunten, Urs

    2016-04-05

    UV/H2O2 processes can be applied to improve the quality of effluents from municipal wastewater treatment plants by attenuating trace organic contaminants (micropollutants). This study presents a kinetic model based on UV photolysis parameters, including UV absorption rate and quantum yield, and hydroxyl radical (·OH) oxidation parameters, including second-order rate constants for ·OH reactions and steady-state ·OH concentrations, that can be used to predict micropollutant abatement in wastewater. The UV/H2O2 kinetic model successfully predicted the abatement efficiencies of 16 target micropollutants in bench-scale UV and UV/H2O2 experiments in 10 secondary wastewater effluents. The model was then used to calculate the electric energies required to achieve specific levels of micropollutant abatement in several advanced wastewater treatment scenarios using various combinations of ozone, UV, and H2O2. UV/H2O2 is more energy-intensive than ozonation for abatement of most micropollutants. Nevertheless, UV/H2O2 is not limited by the formation of N-nitrosodimethylamine (NDMA) and bromate whereas ozonation may produce significant concentrations of these oxidation byproducts, as observed in some of the tested wastewater effluents. The combined process of O3/H2O2 followed by UV/H2O2, which may be warranted in some potable reuse applications, can achieve superior micropollutant abatement with reduced energy consumption compared to UV/H2O2 and reduced oxidation byproduct formation (i.e., NDMA and/or bromate) compared to conventional ozonation.

  8. Synthesis, characterization, magnetic and electrochemical properties of a new 3D hexa-copper-substituted germanotungstate

    Energy Technology Data Exchange (ETDEWEB)

    Li, Yanzhou; Luo, Jie; Zhang, Yanting [Institute of Molecular and Crystal Engineering, Henan Key Lab of Polyoxometalate Chemistry, College of Chemistry and Chemical Engineering, Henan University, Kaifeng, Henan 475004 (China); Zhao, Junwei, E-mail: zhaojunwei@henu.edu.cn [Institute of Molecular and Crystal Engineering, Henan Key Lab of Polyoxometalate Chemistry, College of Chemistry and Chemical Engineering, Henan University, Kaifeng, Henan 475004 (China); Basic Experiment Teaching Center, Henan University, Kaifeng, Henan 475004 (China); Chen, Lijuan, E-mail: ljchen@henu.edu.cn [Institute of Molecular and Crystal Engineering, Henan Key Lab of Polyoxometalate Chemistry, College of Chemistry and Chemical Engineering, Henan University, Kaifeng, Henan 475004 (China); State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002 (China); Ma, Pengtao; Niu, Jingyang [Institute of Molecular and Crystal Engineering, Henan Key Lab of Polyoxometalate Chemistry, College of Chemistry and Chemical Engineering, Henan University, Kaifeng, Henan 475004 (China)

    2013-09-15

    An inorganic–organic hybrid hexa-copper-substituted germanotungstate Na{sub 2}[Cu(dap){sub 2}]{sub 2}[Cu(dap){sub 2}] ([Cu{sub 6}(H{sub 2}O){sub 2}(dap){sub 2}][B-α-GeW{sub 9}O{sub 34}]{sub 2})·4H{sub 2}O (1) (dap=1,2-diaminopropane) has been hydrothermally prepared and characterized by elemental analyses, inductively coupled plasma atomic emission spectrometry (ICP–AES) analyses, IR spectra, powder X-ray diffraction (PXRD), thermogravimetric analysis (TGA) and single-crystal X-ray diffraction. 1 displays the six-connected 3D network with the long topological (O′Keefe) vertex symbol is 4·4·6{sub 4}·4·4·4·4·6{sub 4}·4·4·4·6{sub 4}·4·4·4 and the short vertex (Schläfli) symbol of 4{sup 12}6{sup 3}. Magnetic measurements indicate that there are the overall ferromagnetic exchange interactions in the belt-like hexa-Cu{sup II} cluster in 1. Furthermore, the electrochemical behavior and electrocatalysis of 1 modified carbon paste electrode (1-CPE) have been studied. The reductions of nitrite, bromate and hydrogen peroxide are principally mediated by the W{sup VI}-based wave. - Graphical abstract: A hexa-Cu{sup II} sandwiched germanotungstate has been synthesized and structurally characterized. The magnetic, solid-state electrochemical and electrocatalytic properties have been investigated. Display Omitted - Highlights: • Transition-metal substituted polyoxometalates. • Hexa-copper-substituted germanotungstate. • Six-connected 3D network. • Electrocatalytic reduction of nitrite, bromate and hydrogen peroxide.

  9. Feasibility of wavelength dispersive X-ray fluorescence spectrometry for a simplified analysis of bromine in water samples with the aid of a strong anion exchange disk

    Energy Technology Data Exchange (ETDEWEB)

    An, Jinsung; Jung, Hyeyeon; Bae, Jo-Ri; Yoon, Hye-On, E-mail: dunee@kbsi.re.kr; Seo, Jungju, E-mail: jjseo@kbsi.re.kr

    2014-01-01

    The feasibility of wavelength dispersive X-ray fluorescence spectrometry (WDXRF) for a simplified analysis of bromine (Br) in water samples with the aid of strong anion exchange (SAX) disk was assessed in this study. Dissolved Br in the water sample was pre-concentrated on the SAX disk and directly analyzed by WDXRF without an elution step. The SAX disk was capable of fully adsorbing both bromide (Br{sup −}) and bromate (BrO{sub 3}{sup −}) on its surface owing to their anionic properties, regardless of the pH level of environmental samples. The SAX–WDXRF system was examined using calibration standards (i.e., SAX disks with specific amounts of Br retained; 1, 10, 50, 100 and 500 μg), and a determination coefficient of R{sup 2} = 0.9999 was yielded. The system had a low detection limit for Br (limit of detection = 0.253 μg for Br on the SAX disk) with good reproducibility (relative standard error (RSE) = 4–7%). Spike and inter-comparison tests were performed to confirm the accuracy of the proposed SAX–WDXRF method. Both tests exhibited reasonable accuracy (RSE = 3–6%). The method is simple and easy, indicating a great possibility of application in various environmental sample types, especially for which a simplified analytical system for the determination of Br is urgently required. - Highlights: • Bromide and bromate were entirely retained on a strong anion exchange (SAX) disk. • The SAX disk was used to pre-concentrate dissolved Br species from water samples. • The SAX disk adsorbing dissolved Br was directly analyzed by WDXRF. • The accuracy of the SAX–WDXRF method was confirmed by spike and inter-comparison tests. • Rapid and sensitive Br analysis can be achieved using the proposed SAX–WDXRF method.

  10. Graft copolymer (chitosan-g-N-vinyl formamide): Synthesis and study of its properties like swelling, metal ion uptake and flocculation

    Energy Technology Data Exchange (ETDEWEB)

    Mishra, D.K.; Tripathy, J.; Srivastava, A.; Mishra, M.M.; Behari, K. [University of Allahabad, Allahabad (India). Dept. of Chemistry

    2008-11-04

    A graft copolymer of chitosan and N-vinyl formamide has been synthesized by free radical polymerization using bromate/cyclohexanone redox in an inert atmosphere. The grafting ratio, add on, and efficiency increase continuously with increase in concentration of N-vinyl formamide from 9 x 10{sup -2} mol dm{sup -3} to 41 x 10{sup -2} mol dm{sup -3}, bromate ion from 0.4 x 10{sup -2} mol dm{sup -3} to 2.4 x 10{sup -2} mol dm{sup -3} and chitosan from 0.6 g dm{sup -3} to 1.4 g dm{sup -3}. Grafting parameters decrease with increase in concentration of hydrogen ion from 2 x 10{sup -3} mol dm{sup -3} to 10 x 10{sup -3} mol dm{sup -3}. Experimental results also show that these parameters i.e. grafting ratio, add on, and efficiency increase with increase in cyclohexanone concentration from 0.4 x 10{sup -2} mol dm{sup -3} to 1.2 x 10{sup -2} mol dm{sup -3}, but beyond this cited range, these parameters decrease. Maximum grafting i.e. 189.5% has been found at 120 min and 40{sup o}C. The swelling, metal ion sorption and flocculation capability have been studied, respectively. The flocculation capability of chitosan and chitosan-g-N-vinyl formamide in both coking and non-coking coals has been studied for the treatment of coal mine waste water. The graft copolymer has been characterized by infra red (IR) spectroscopy and thermogravimetric analysis.

  11. BROMATOMATRIC ASSAY OF GATIFLOXACIN IN PHARMACEUTICALS

    Directory of Open Access Journals (Sweden)

    KALSANG THARPA

    2008-09-01

    Full Text Available Three new, simple, and cost-effective visible spectrophotometric methods are proposed for determination of gatifloxacin (GTF using bromate-bromide mixture, and three dyes, methyl orange, indigocarmine and thymol blue, as reagents.The methods engross the addition of a known excess of bromate-bromide mixture to GTF in hydrochloric acid medium followed by determination of residual bromine by reacting with a fixed amount of either methyl orange andmeasuring the absorbance at 520 nm (method A or indigo carmine and measuring the absorbance at 610 nm (method B or thymol blue and measuring the absorbance at 550 nm (method C. In all the methods, the amount of brominereacted corresponds to the amount of GTF, and the absorbance is found to increase linearly with the concentration of GTF. Under the optimum conditions, GTF could be assayed in the concentration range 0.25-1.5, 0.5-6.0, and 0.5-10μg/mL by method A, method B and method C, respectively. The apparent molar absorptivities are calculated to be 1.6x105, 4.0x104 and 3.2x104 L mol-1 cm-1 for the method A, method B and method C, respectively, and the corresponding Sandell sensitivity values are 0.0025, 0.010 and 0.012 μg/cm2. The intra-day and inter-day precision, and the accuracy of the methods were evaluated as per the current ICH guidelines. The methods were successfully applied to the determination of GTF in pharmaceutical preparations without the interference from any of the pharmaceutical adjuvants.

  12. Evaluation of a full-scale wastewater treatment plant upgraded with ozonation and biological post-treatments: Abatement of micropollutants, formation of transformation products and oxidation by-products.

    Science.gov (United States)

    Bourgin, Marc; Beck, Birgit; Boehler, Marc; Borowska, Ewa; Fleiner, Julian; Salhi, Elisabeth; Teichler, Rebekka; von Gunten, Urs; Siegrist, Hansruedi; McArdell, Christa S

    2018-02-01

    sorption. The relative abatement of the indicator substances ranged between 20 and 89% after 27'000 bed volumes (BV) and was still substantial at 50'000 BV. In an identical GAC filter running in parallel and being fed with the effluent of the secondary clarifier, the elimination was less efficient. Seven primary OTPs (chlorothiazide and six N-oxides) formed during ozonation could be quantified thanks to available reference standards. Their concentration decreased with increasing specific ozone doses with the concomitant formation of other OTPs. The seven OTPs were found to be stable compounds and were not abated in the biological post-treatments. They were sorbed in the fresh GAC filter, but less efficiently than the corresponding parent compounds. Two OBPs, bromate (BrO3-) and N-nitrosodimethylamine (NDMA), were formed during ozonation but did not exceeded 5 μg/L for bromate and 30 ng/L for NDMA at the recommended specific ozone dose of 0.55 g O3/g DOC. NDMA was well abated in all post-treatments (minimum 41% during fixed bed filtration, maximum 83% during fresh GAC filtration), while bromate was very stable as expected. Copyright © 2017 Elsevier Ltd. All rights reserved.

  13. Bromide, Chloride, and Sulfate Concentrations, and Specific Conductance, Lake Texoma, Texas and Oklahoma, 2007-08

    Science.gov (United States)

    Baldys, Stanley

    2009-01-01

    The U.S. Geological Survey, in cooperation with the City of Dallas Water Utilities Division, collected water-quality data from 11 sites on Lake Texoma, a reservoir on the Texas-Oklahoma border, during April 2007-September 2008. At 10 of the sites, physical properties (depth, specific conductance, pH, temperature, dissolved oxygen, and alkalinity) were measured and samples were collected for analysis of selected dissolved constituents (bromide, calcium, magnesium, potassium, sodium, carbonate, bicarbonate, chloride, and sulfate); at one site, only physical properties were measured. The primary constituent of interest was bromide. Bromate can form when ozone is used to disinfect raw water containing bromide, and bromate is a suspected human carcinogen. Chloride and sulfate were of secondary interest. Only the analytical results for bromide, chloride, sulfate, and measured specific conductance are discussed in this report. Median dissolved bromide concentrations ranged from 0.28 to 0.60 milligrams per liter. The largest median dissolved bromide concentration (0.60 milligram per liter at site 11) was from the Red River arm of Lake Texoma. Dissolved bromide concentrations generally were larger in the Red River arm of Lake Texoma than in the Washita arm of the lake. Median dissolved chloride concentrations were largest in the Red River arm of Lake Texoma at site 11 (431 milligrams per liter) and smallest at site 8 (122 milligrams per liter) in the Washita arm. At site 11 in the Red River arm, the mean and median chloride concentrations exceeded the secondary maximum contaminant level of 300 milligrams per liter for chloride established by the 'Texas Surface Water Quality Standards' for surface-water bodies designated for the public water supply use. Median dissolved sulfate concentrations ranged from 182 milligrams per liter at site 4 in the Big Mineral arm to 246 milligrams per liter at site 11 in the Red River arm. None of the mean or median sulfate concentrations

  14. Fabrication, electrochemical and electrocatalytic properties of carbon nanotube@nano-SiO{sub 2}BenV/phosphomolybdic acid polynary nanocomposite materials

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Jiang; Wang, Jing; Wang, Wen-Bo [Department of Chemistry, Fudan University, 220 Handan Road, Shanghai 200433 (China); Chen, Meng [Department of Material Science, Fudan University, 220 Handan Road, Shanghai 200433 (China); Qian, Dong-Jin, E-mail: djqian@fudan.edu.cn [Department of Chemistry, Fudan University, 220 Handan Road, Shanghai 200433 (China)

    2017-06-30

    Highlights: • Carbon nanotube@nano-SiO{sub 2}BenV(+86-21-65643666)/PMA polynary nanocomposites were prepared. • Functionalized silica nanoparticles covalently attached on the MWNT surfaces. • The nanocomposites showed reversible redox properties of viologen and PMA. • The nanocomposites acted as efficient heterogeneous catalysts for bromate reduction. - Abstract: Organic-inorganic nano-materials have attracted growing attention due to their potential applications for optoelectronic devices, sensors, and heterogeneous catalysts. We reported here on the preparation of polynary nanocomposites composed of poly(4-vinylpyridine) (P4VP) functionalized multi-walled carbon nanotubes (MWNTP4VP), silica nanoparticles (nano-SiO{sub 2}), viologens, and/or phosphomolybdic acid (PMA), in which the MWNTP4VP, nano-SiO{sub 2}, and viologens were covalently connected while PMA was electrostatically adsorbed. Thermogravimetric analysis revealed that the nanocomposites were composed of about 40–45% MWNTs, 40–45% nanoSiO{sub 2}, as well as 10–15% organic species and others. The preparation processes and compositions of the nanocomposites were characterized using Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. Field emission transmission electron microscopic images revealed that the nano-SiO{sub 2}BenV particles were strongly attached to the MWNTP4VP surfaces to form MWNTP4VP@nano-SiO{sub 2}BenV triad nano-cores. Cyclic voltammograms of the MWNTP4VP@nano-SiO{sub 2}BenV casting films showed three couples of redox waves in the potential range between −0.8 and 0 V (vs Ag/AgCl), designated to the electron transfer process of viologen substituents of MWNTP4VP@nano-SiO{sub 2}BenV{sup 2+} ↔ MWNTP4VP@nano-SiO{sub 2}BenV{sup +}· and their dimers. Further, three couples of redox waves were recorded for the casting films of MWNTP4VP@nano-SiO{sub 2}BenV/PMA polynary nanocomposites in the potential range between −0.2 and 0.8 V, designated to three

  15. Analysis of Diurnal Variations in Energy Footprint and Its Associated Carbon Emission for Water Supply and Reuse in Arid and Semi-Arid Areas

    Science.gov (United States)

    Sobhani, Reza

    characterized by water scarcity, such as Southern California, groundwater containing chromophoric dissolved organic matter is a viable source of water supply. However, the seawater intrusion increased the concentration of bromide in extracted groundwater. Bromide, a precursor to bromate formation is regulated by USEPA as a potential carcinogen. This study compares the energy footprint among the two processes utilized for treatment of highly colored groundwater (i.e. nanofiltration and ozone injection coupled with biologically activated carbon) and discusses the impacts of bromate formation among these processes.

  16. Interaction of inorganic anions with iron-mineral adsorbents in aqueous media--a review.

    Science.gov (United States)

    Kumar, Eva; Bhatnagar, Amit; Hogland, William; Marques, Marcia; Sillanpää, Mika

    2014-01-01

    A number of inorganic anions (e.g., nitrate, fluoride, bromate, phosphate, and perchlorate) have been reported in alarming concentrations in numerous drinking water sources around the world. Their presence even in very low concentrations may cause serious environmental and health related problems. Due to the presence and significance of iron minerals in the natural aquatic environment and increasing application of iron in water treatment, the knowledge of the structure of iron and iron minerals and their interactions with aquatic pollutants, especially inorganic anions in water are of great importance. Iron minerals have been known since long as potential adsorbents for the removal of inorganic anions from aqueous phase. The chemistry of iron and iron minerals reactions in water is complex. The adsorption ability of iron and iron minerals towards inorganic anions is influenced by several factors such as, surface characteristics of the adsorbent (surface area, density, pore volume, porosity, pore size distribution, pHpzc, purity), pH of the solution, and ionic strength. Furthermore, the physico-chemical properties of inorganic anions (pore size, ionic radius, bulk diffusion coefficient) also significantly influence the adsorption process. The aim of this paper is to provide an overview of the properties of iron and iron minerals and their reactivity with some important inorganic anionic contaminants present in water. It also summarizes the usage of iron and iron minerals in water treatment technology. © 2013.

  17. Evaluating hydraulic and disinfection efficiencies of a full-scale ozone contactor using a RANS-based modeling framework.

    Science.gov (United States)

    Zhang, Jie; Tejada-Martínez, Andrés E; Zhang, Qiong; Lei, Hongxia

    2014-04-01

    The capability of predicting hydraulic and disinfection efficiencies of ozone disinfection contactors is essential for evaluating existing contactors and improving future designs. Previous attempts based on ideal and non-ideal models for the hydraulics and simplified mechanisms for chemical reaction modeling have resulted in low accuracy and are restricted to contactors with simple geometries. This manuscript develops a modeling framework for the ozonation process by combining computational fluid dynamics (CFD) with a kinetics-based reaction modeling for the first time. This computational framework has been applied to the full-scale ozone contactor operated by the City of Tampa Water Department. Flow fields, residence time distribution, ozone concentration distribution, and concentration-contact time (CT) distribution within the contactor have been predicted via the computational framework. The predictions of ozone and bromate concentrations at sample points agree well with physical experimental data measured in the contactor. The predicted CT values at the contactor outlet demonstrate that the disinfection performance of the ozone contactor operated by the City of Tampa Water Department is sufficient to meet regulation requirements. The impact of seasonal flow rate change on disinfection performance is found to be significant and deserves attention during the management and operation of a water treatment plant. Copyright © 2014 Elsevier Ltd. All rights reserved.

  18. A sensitive colorimetric method for the determination of nitrite in water supplies, meat and dairy products using ionic liquid-modified methyl red as a colour reagent.

    Science.gov (United States)

    Zhang, Haijuan; Qi, Shengda; Dong, Yalei; Chen, Xiaojiao; Xu, Yinyin; Ma, Yanhua; Chen, Xingguo

    2014-05-15

    This paper describes a colorimetric approach to determine trace amounts of nitrite in water supplies, meat and dairy products using 1-butyl-3-methylimidazolium-modified methyl red ([BMIM]MR) as a colour reagent. The technique capitalises on the catalytic effect of nitrite on the oxidative degradation of [BMIM]MR by potassium bromate in acidic media. The absorbances were proportional to nitrite concentrations in the range of 8.70×10(-2) to 4.17 μM with a detection limit of 1.64×10(-2) μM. Compared with the method using methyl red as a colour reagent, 60 times improvement of sensitivity was obtained. Activation energy and the apparent rate constant for the catalytic reaction are 61.11 kJ mol(-1) and 1.18×10(4) s(-1), respectively. The proposed method was successfully applied for the analysis of nitrite in Yellow River water, chicken, and milk with recoveries ranging from 96% to 105%. Copyright © 2013 Elsevier Ltd. All rights reserved.

  19. Enhancement of oxyanion and diatrizoate reduction kinetics using selected azo dyes on Pd-based catalysts.

    Science.gov (United States)

    Shuai, Danmeng; Chaplin, Brian P; Shapley, John R; Menendez, Nathaniel P; McCalman, Dorrell C; Schneider, William F; Werth, Charles J

    2010-03-01

    Azo dyes are widespread pollutants and potential cocontaminants for nitrate; we evaluated their effect on catalytic reduction of a suite of oxyanions, diatrizoate, and N-nitrosodimethylamine (NDMA). The azo dye methyl orange significantly enhanced (less than or equal to a factor of 5.24) the catalytic reduction kinetics of nitrate, nitrite, bromate, perchlorate, chlorate, and diatrizoate with several different Pd-based catalysts; NDMA reduction was not enhanced. Nitrate was selected as a probe contaminant, and a variety of azo dyes (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. Hydrogenation energies of azo dyes were calculated using density functional theory and a volcano relationship between hydrogenation energies and reduction rate enhancement was observed. A kinetic model based on Brønsted-Evans-Polanyi (BEP) theory matched the volcano relationship and suggests sorbed azo dyes enhance reduction kinetics through hydrogen atom shuttling between reduced azo dyes (i.e., hydrazo dyes) and oxyanions or diatrizoate. This is the first research that has identified this synergetic effect, and it has implications for designing more efficient catalysts and reducing Pd costs in water treatment systems.

  20. Bayesian analysis of physiologically based toxicokinetic and toxicodynamic models.

    Science.gov (United States)

    Hack, C Eric

    2006-04-17

    Physiologically based toxicokinetic (PBTK) and toxicodynamic (TD) models of bromate in animals and humans would improve our ability to accurately estimate the toxic doses in humans based on available animal studies. These mathematical models are often highly parameterized and must be calibrated in order for the model predictions of internal dose to adequately fit the experimentally measured doses. Highly parameterized models are difficult to calibrate and it is difficult to obtain accurate estimates of uncertainty or variability in model parameters with commonly used frequentist calibration methods, such as maximum likelihood estimation (MLE) or least squared error approaches. The Bayesian approach called Markov chain Monte Carlo (MCMC) analysis can be used to successfully calibrate these complex models. Prior knowledge about the biological system and associated model parameters is easily incorporated in this approach in the form of prior parameter distributions, and the distributions are refined or updated using experimental data to generate posterior distributions of parameter estimates. The goal of this paper is to give the non-mathematician a brief description of the Bayesian approach and Markov chain Monte Carlo analysis, how this technique is used in risk assessment, and the issues associated with this approach.

  1. Inactivation of invasive marine species in the process of conveying ballast water using OH based on a strong ionization discharge.

    Science.gov (United States)

    Bai, Mindong; Zheng, Qilin; Tian, Yiping; Zhang, Zhitao; Chen, Cao; Cheng, Chao; Meng, Xiangying

    2016-06-01

    In this paper, invasive marine species in medium-salinity ballast water were inactivated using OH generated from a strong ionization discharge. The OH is determined by the concentration of oxygen active species combined with the effects of water jet cavitation. The results indicated that the OH concentration reached 7.62 μM, within 1 s, which is faster and higher than in conventional AOP methods. In a pilot-scale OH ballast water system with a capacity of 10 m(3)/h, algae were inactivated when CT value was 0.1 mg min/L with a contact time only 6 s. The viable and nonviable cells were determined using SYTOX Green nucleic acid stain and Flow cytometry. As a result, the OH treatment could be completed during the process of conveying the ballast water. In addition, the concentrations of relevant disinfection by-products (DBPs), such as trihalomethanes (THMs), haloacetic acids (HAAs), and bromate, were less than that required by the World Health Organization's drinking water standards, which suggest that the discharged ballast water posed no risks to the oceanic environment. Nevertheless, for conventional ozonation and electrolysis methods, the ballast water should be treated only in the treated tanks during the ship's voyage and form higher level DBPs. Copyright © 2016 Elsevier Ltd. All rights reserved.

  2. The advanced EctoSys electrolysis as an integral part of a ballast water treatment system.

    Science.gov (United States)

    Echardt, J; Kornmueller, A

    2009-01-01

    A full-scale 500 m(3)/h ballast water treatment system was tested according to the landbased type approval procedure of the International Maritime Organization (IMO). The system consists of disc filters followed by the advanced EctoSys electrolysis as an integral part for disinfection. The test water quality exceeded by far the minimum requirements for type approval testing. Due to the properties of the special electrodes used together with the striking disinfection effect, the disinfectants assumed to be produced inline by the EctoSys cell in river water were hydroxyl radicals, while in brackish water additionally chlorine and consequently the more stable bromine were formed. In river water, no residual oxidants could be detected in accordance with the assumed production of not responding, highly-reactive and short-living hydroxyl radicals. Accordingly, disinfection byproduct (DBP) formation was very low and close to the limit of quantification in river water. While in brackish water, initial residual oxidant concentrations were maximum 2 mg/L as chlorine and mostly brominated DBP (especially bromoform and bromate) were found. Overall considering this worst case test approach, the DBP concentrations of the treated effluents were below or in the range of the WHO Drinking Water Guideline values and therefore evaluated as acceptable for discharge to the environment. The stringent discharge standard by IMO concerning viable organisms was fully met in river and brackish water, proving the disinfection efficiency of the EctoSys electrolysis against smaller plankton and bacteria.

  3. Photocatalytic degradation of a widely used insecticide Thiamethoxam in aqueous suspension of TiO2: adsorption, kinetics, product analysis and toxicity assessment.

    Science.gov (United States)

    Mir, Niyaz A; Khan, A; Muneer, M; Vijayalakhsmi, S

    2013-08-01

    This paper deals with the study of photocatalyzed degradation of an insecticide, Thiamethoxam in aqueous suspension of TiO2. The adsorption of Thiamethoxam on TiO2 surface under dark conditions was also investigated in order to find out equilibrium adsorption constant. The degradation kinetics was studied using spectrophotometric method under various conditions such as substrate concentration, type of catalyst, catalyst dosage, pH, and in the presence of electron acceptors such as hydrogen peroxide, potassium bromate, and ammonium persulphate under continuous purging of atmospheric oxygen, and the degradation rates were found to be strongly influenced by these parameters. The results manifested that the photocatalysis of Thiamethoxam follows pseudo-first-order kinetics. The toxicity assessments of the irradiated samples were carried out using human erythrocytes as a model system under in vitro conditions. GC-MS study showed the formation of several intermediate products which were characterised based on their molecular mass and mass fragmentation pattern. A probable mechanism for the formation of various products formed during the photocatalytic process of Thiamethoxam was also proposed. Copyright © 2013 Elsevier B.V. All rights reserved.

  4. New inorganic (an)ion exchangers based on Mg–Al hydrous oxides: (Alkoxide-free) sol–gel synthesis and characterisation

    KAUST Repository

    Chubar, Natalia

    2011-05-01

    New inorganic ion exchangers based on double Mg-Al hydrous oxides were generated via the new non-traditional sol-gel synthesis method which avoids using metal alkoxides as raw materials. Surface chemical and adsorptive properties of the final products were controlled by several ways of hydrogels and xerogels treatments which produced the materials of the layered structure, mixed hydrous oxides or amorphous adsorbents. The final adsorptive materials obtained via thermal treatment of xerogels were the layered mesoporous materials with carbonate in the interlayer space, surface abundance with hydroxylic groups and maximum adsorptive capacity to arsenate. Higher affinity of Mg-Al hydrous oxides towards H2AsO4- is confirmed by steep adsorption isotherms having plateau (removal capacity) at 220. mg[As]. gdw-1 for the best sample at pH = 7, fast adsorption kinetics and little pH effect. Adsorption of arsenite, fluoride, bromate, bromide, selenate, borate by Mg-Al hydrous oxides was few times high either competitive (depending on the anion) as compare with the conventional inorganic ion exchange adsorbents. © 2011 Elsevier Inc.

  5. An on-line spectrophotometric determination of trace amounts of thiourea in tap water, orange juice, and orange peel samples using multi-channel flow injection analysis.

    Science.gov (United States)

    Arab Chamjangali, M; Goudarzi, N; Ghochani Moghadam, A; Amin, A H

    2015-01-01

    In this work, a flow injection analysis (FIA) method was introduced for the determination of trace amounts of thiourea in tap water. This method is based upon the inhibition effect of thiourea on the reaction between meta-cresol purple (MCP) and potassium bromate catalyzed by bromide ions in a sulfuric acid medium. In the presence of thiourea, an induction period appears in the reaction system, and as a result, the absorbance of MCP increases at 525 nm in the FIA manifold. The chemical and FIA variables are studied and optimized using the univariate and Simplex optimization methods. Under the optimum conditions, thiourea can be determined in the range of 0.100-13.0 μg mL(-1). The limit of detection (3σ) for thiourea was found to be 0.0310 μg mL(-1). The relative standard deviations (RSDs) for six replicate determinations of 0.500, 5.00, and 12.0 μg mL(-1) of thiourea were 4.0%, 1.8%, and 1.2%, respectively. The proposed method was also applied for the determination of thiourea in orange juice and orange peel samples with recoveries in the range of 98.0-101%. The analytical speed of the method was calculated to be about 120 sample per hour. Copyright © 2015 Elsevier B.V. All rights reserved.

  6. Solar photocatalytic H{sub 2} production from water using a dual bed photosystem

    Energy Technology Data Exchange (ETDEWEB)

    Linkous, C.A. [Florida Solar Energy Center, Cocoa, FL (United States)

    1996-10-01

    The authors are developing a dual stage, direct photoconversion scheme for water splitting. The overall system consists of an aqueous solution circulated through two modules, or beds, each of which contains a photochemically active surface layer below the solution. The idea is to divide the energy requirement for water decomposition between the two photosystems, so that more abundant, lower energy photons in the solar spectrum can be utilized, and that the H{sub 2} and O{sub 2} products can be evolved separately from each other. Catalyst-modified semiconductor powders, immobilized within a polymer binder are currently being employed as the photoactive layers. TiO{sub 2} and platinized-InP have been employed for the O{sub 2} and H{sub 2} evolution tasks, respectively. A major effort over the last year was identification of a suitable redox mediator that is responsible for transferring electron equivalents from one unit to the other. After testing more than a dozen candidates, spanning a wide range of electropotentials, under a variety of conditions, it was found that the bromide/bromate (Br{sup {minus}}/BrO{sub 3}{sup {minus}}) and iodide/iodate (I{sup {minus}}/IO{sub 3}{sup {minus}}) redox systems could function in both modules, necessary for closed cycle operation.

  7. Control of the red tide dinoflagellate Cochlodinium polykrikoides by ozone in seawater.

    Science.gov (United States)

    Shin, Minjung; Lee, Hye-Jin; Kim, Min Sik; Park, Noh-Back; Lee, Changha

    2017-02-01

    The inactivation of C. polykrikoides, a red tide dinoflagellate, by ozonation was investigated in seawater by monitoring numbers of viable and total cells. Parameters affecting the inactivation efficacy of C. polykrikoides such as the ozone dose, initial cell concentration, pH, and temperature were examined. The viable cell number rapidly decreased in the initial stage of the reaction (mostly in 1-2 min), whereas the decrease in total cell number was relatively slow and steady. Increasing ozone dose and decreasing initial cell concentration increased the inactivation efficacy of C. polykrikoides, while increasing pH and temperature decreased the cell inactivation efficacy. The addition of humic acid (a promoter for the ozone decomposition) inhibited the inactivation of C. polykrikoides, whereas bicarbonate ion (an inhibitor for the ozone decomposition) accelerated the C. polykrikoides inactivation. Observations regarding the effects of pH, temperature, humic acid, and bicarbonate ion collectively indicate that the inactivation of C. polykrikoides by ozonation is mainly attributed to oxidative cell damages by molecular ozone, rather than by hydroxyl radical, produced during the ozone decomposition. At high ozone dose (e.g., 5 mg/L), hypobromous acid formed by the reaction of bromide with ozone may partially contribute to cell inactivation. The use of ozone of less than 1 mg/L produced 0.75-2.03 μg/L bromate. Copyright © 2016 Elsevier Ltd. All rights reserved.

  8. Photocatalytic degradation of a widely used insecticide Thiamethoxam in aqueous suspension of TiO{sub 2}: Adsorption, kinetics, product analysis and toxicity assessment

    Energy Technology Data Exchange (ETDEWEB)

    Mir, Niyaz A.; Khan, A. [Department of Chemistry, Aligarh Muslim University, Aligarh-202002, UP (India); Muneer, M., E-mail: readermuneer@gmail.com [Department of Chemistry, Aligarh Muslim University, Aligarh-202002, UP (India); Vijayalakhsmi, S. [SAIF, CRNTS, IIT Bombay, Powai, 400076, Mumbai (India)

    2013-08-01

    This paper deals with the study of photocatalyzed degradation of an insecticide, Thiamethoxam in aqueous suspension of TiO{sub 2}. The adsorption of Thiamethoxam on TiO{sub 2} surface under dark conditions was also investigated in order to find out equilibrium adsorption constant. The degradation kinetics was studied using spectrophotometric method under various conditions such as substrate concentration, type of catalyst, catalyst dosage, pH, and in the presence of electron acceptors such as hydrogen peroxide, potassium bromate, and ammonium persulphate under continuous purging of atmospheric oxygen, and the degradation rates were found to be strongly influenced by these parameters. The results manifested that the photocatalysis of Thiamethoxam follows pseudo-first-order kinetics. The toxicity assessments of the irradiated samples were carried out using human erythrocytes as a model system under in vitro conditions. GC–MS study showed the formation of several intermediate products which were characterised based on their molecular mass and mass fragmentation pattern. A probable mechanism for the formation of various products formed during the photocatalytic process of Thiamethoxam was also proposed. Highlights: • TiO{sub 2} P25 is a more efficient photocatalyst than UV100 and PC500 for degradation of Thiamethoxam. • Low H{sub 2}O{sub 2} dosages enhance degradation whereas overdose retards it. • Toxicity of Thiamethoxam decreases with the increase in irradiation time. • Eight intermediate products have been identified using GC–MS analysis technique.

  9. Oxidative Stress in the Carcinogenicity of Chemical Carcinogens

    Directory of Open Access Journals (Sweden)

    Hideki Wanibuchi

    2013-10-01

    Full Text Available This review highlights several in vivo studies utilizing non-genotoxic and genotoxic chemical carcinogens, and the mechanisms of their high and low dose carcinogenicities with respect to formation of oxidative stress. Here, we survey the examples and discuss possible mechanisms of hormetic effects with cytochrome P450 inducers, such as phenobarbital, a-benzene hexachloride and 1,1-bis(p-chlorophenyl-2,2,2-trichloroethane. Epigenetic processes differentially can be affected by agents that impinge on oxidative DNA damage, repair, apoptosis, cell proliferation, intracellular communication and cell signaling. Non-genotoxic carcinogens may target nuclear receptors and induce post-translational modifications at the protein level, thereby impacting on the stability or activity of key regulatory proteins, including oncoproteins and tumor suppressor proteins. We further discuss role of oxidative stress focusing on the low dose carcinogenicities of several genotoxic carcinogens such as a hepatocarcinogen contained in seared fish and meat, 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline, arsenic and its metabolites, and the kidney carcinogen potassium bromate.

  10. Effects of operating conditions on THMs and HAAs formation during wastewater chlorination

    Energy Technology Data Exchange (ETDEWEB)

    Sun Yingxue; Wu Qianyuan [Environmental Simulation and Pollution Control State Key Joint Laboratory, Department of Environmental Science and Engineering, Tsinghua University, Beijing 100084 (China); Hu Hongying, E-mail: hyhu@tsinghua.edu.cn [Environmental Simulation and Pollution Control State Key Joint Laboratory, Department of Environmental Science and Engineering, Tsinghua University, Beijing 100084 (China); Tian Jie [Environmental Simulation and Pollution Control State Key Joint Laboratory, Department of Environmental Science and Engineering, Tsinghua University, Beijing 100084 (China)

    2009-09-15

    Disinfection is the last barrier of wastewater reclamation process to protect ecosystem safety and human health. However, the chlorination process results in the formation of mutagenic/carcinogenic disinfection by-products (DBPs) deriving from the reaction of the chlorine with organic compounds in wastewater. The effects of operating conditions (chlorine dose, contact time, reaction temperature and pH value) of chlorination on the formation of trihalomethanes (THMs) and haloacetic acids (HAAs) in biologically treated wastewater samples were investigated in this study. The results indicated that the total THMs (TTHM) and total HAAs (THAA) increased exponentially with increasing chlorine dose, but there are discrepancies between the formation rates of TTHM and THAA. The THAA reached a peak at contact time of 2 h and thereafter decreased with extended time. The formation time of THMs depends on the wastewater content of quick or slow formers. The yields of bromated HAAs (as MBAA, BCAA, and BDCAA) would decrease markedly after the contact time over 2 h during wastewater chlorination, and were favored in low pH values of 4 and high pH values of 9 under certain contact time. In addition, the formation of MBAA, BCAA, BDCAA decreased gradually as reaction temperature increased from 4 to 30 deg. C in the chlorination of wastewater containing a certain concentration of bromide. The effects of operating conditions on THMs and HAAs formation during wastewater chlorination were completely different from those of surface water disinfection.

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

    Energy Technology Data Exchange (ETDEWEB)

    Luca, Gilmara Caseri de

    1996-02-01

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

  12. Protective effects of bilberry (Vaccinium myrtillus L.) extract on KBrO3-induced kidney damage in mice.

    Science.gov (United States)

    Bao, Li; Yao, Xin-Sheng; Tsi, Daniel; Yau, Chin-Chin; Chia, Chew-Sern; Nagai, Hajime; Kurihara, Hiroshi

    2008-01-23

    Potassium bromate (KBrO3) is an oxidizing agent used as a food additive which causes kidney damage as a potent nephrotoxic agent, and the mechanism may be explained by the generation of oxygen free radicals. Our experiments showed that single intraperitoneal administration of 200 mg/kg KBrO3 could induce serious kidney damage, with an increase in serum blood urea nitrogen (BUN) and creatinine levels. Five-day oral administration of bilberry ( Vaccinium myrtillus L.) extract at 50, 100, and 200 mg/kg resulted in a reversal in serum BUN and creatinine to normal levels and decreased kidney malondialdehyde (MDA), nitric oxide (NO), and xanthine oxidase (XOD) levels. Also, bilberry extract improved oxygen radical absorbance capacity (ORAC) levels in kidney tissue, which showed that bilberry extract reduced the degree of oxidative stress and kidney damage induced by KBrO3. These findings demonstrate that the protective effect of bilberry extract is attributed to its free radical scavenging activity and lipid peroxidation inhibitory effect.

  13. PIXE analysis of Nigerian flour and bread samples

    Energy Technology Data Exchange (ETDEWEB)

    Olise, Felix S., E-mail: felix_olise@rushpost.com [Department of Physics, Obafemi Awolowo University, Ile-Ife 220005 (Nigeria); Fernandes, Adriana M.; Cristina Chaves, P. [CFA: Centro de Física Atómica da Universidade de Lisboa, Av. Prof. Gama Pinto 2, 1649-003 Lisboa (Portugal); Taborda, Ana; Reis, Miguel A. [IST/CTN: Instituto Superior Técnico, Universidade Técnica de Lisboa, Campus Tecnológico e Nuclear (CTN), EN10, 2686-953 Sacavém (Portugal); CFA: Centro de Física Atómica da Universidade de Lisboa, Av. Prof. Gama Pinto 2, 1649-003 Lisboa (Portugal)

    2014-01-01

    Highlights: • The PIXE technique has been used to determine K and Br in a major Nigerian food item. • Samples were analysed using two proton beam energies, namely 1.25 MeV and 2.15 MeV. • Mismatched Ca results reflect its nature and accuracy/precision of the procedure. • Explanations for the presence of the contaminant in the samples are presented. • Other sources originating from erroneous burning of dangerous products suspected. -- Abstract: The alleged use of potassium bromate (KBrO{sub 3}) in bread baking led a few authors to report on the chemical methods for the determination of KBrO{sub 3} levels in bread. In order to examine the potentials of a non chemical particle induced X-ray emission (PIXE) method for this purpose, six sets of samples, each composed of flour, dough and bread from a production batch were analysed. The samples were obtained from six different bakers of bread at Ile-Ife, Nigeria. The flour samples were air-dried while others were freeze dried at about −16 °C. The samples were homogenised in an agate mortar and then pelletised. Samples were analysed at the CTN standard PIXE setup and standard procedures for thick target samples analysis were followed. In some samples significant concentrations of bromine were found. In the present work we present possible explanations for the presence of this potentially dangerous contaminant in the samples.

  14. Polyoxometallates as inorganic templates for electrocatalytic network films of ultra-thin conducting polymers and platinum nanoparticles.

    Science.gov (United States)

    Karnicka, Katarzyna; Chojak, Malgorzata; Miecznikowski, Krzysztof; Skunik, Magdalena; Baranowska, Beata; Kolary, Aneta; Piranska, Aleksandra; Palys, Barbara; Adamczyk, Lidia; Kulesza, Pawel J

    2005-04-01

    We develop a concept of fabrication of the multilayer network films on electrodes by exploring the ability of a Keggin-type polyoxometallate, phosphododecamolybdate (PMo(12)O(40)(3-)), to form stable anionic monolayers (templates) on carbon and metals including platinum. By repeated alternate treatments in the solution of PMo(12)O(40)(3-) (or in the colloidal suspension of polyoxometallate-protected Pt-nanoparticles) and in the solution of monomer (e.g. anilinium) cations, the amount of the material can be increased systematically (layer-by-layer) to form stable three-dimensional assemblies on electrode (e.g. glassy carbon) surfaces. In the resulting hybrid (organic-inorganic) films, the layers of negatively charged polyoxometallate, or polyoxometallate-protected (stabilized) Pt-nanoparticles, are linked or electrostatically attracted by ultra-thin layers of such positively charged conducting polymers as polyaniline (PANI), polypyrrole (PPy) or poly(3,4-ethylenedioxythiophene), PEDOT. Consequently, the attractive physicochemical properties of polymers and reactivity of polyoxometallate or noble metal particles are combined. The films are functionalized and show electrocatalytic properties towards reduction of nitrite, bromate, hydrogen peroxide or oxygen. They are of importance to the chemical and biochemical sensing as well as to the biochemical and medical applications.

  15. Sensitive Bromatometric Methods for the Determination of Sumatriptan Succinate in Pharmaceutical Formulations

    Directory of Open Access Journals (Sweden)

    K. V. V. Satyanarayana

    2011-01-01

    Full Text Available Two simple and sensitive spectrophotometric methods are described for the determination of sumatriptan succinate (STS in pure and tablets using bromate-bromide as the bromination reagent in acid medium and two dyes as subsidiary reagents. The two methods are based on the bromination of STS by a known excess of in situ generated bromine followed by determination of unreacted bromine by reacting with a fixed amount of methyl orange (Method A or indigo carmine (Method B and measuring the absorbance at 508 or 610 nm. In both methods, the amount of bromine reacted corresponds to the amount of STS. The experimental conditions for the assay have been optimized. In two methods, the absorbance was found to increase linearly with the concentration of STS at the respective wavelengths. Beer’s law was obeyed over the ranges 0.2-1.6 and 2.0-12.0 μg mL-1 for method A and method B respectively and the respective molar absorptivity values were 1.898×105 and 2.71×104 L mol-1 cm-1. The statistical analysis of the methods was validated according to the present ICH guidelines. The proposed methods were applied to the analysis of tablet form of STS and the results tallied well with the label claim.

  16. Integration of vanadium-mixed addenda Dawson heteropolytungstate within poly(3,4-ethylenedioxythiophene) and poly(2,2'-bithiophene) films by electrodeposition from the nonionic micellar aqueous medium

    Energy Technology Data Exchange (ETDEWEB)

    Goral, Monika [Department of Chemistry, University of Warsaw, Pasteura 1, 02-093 Warsaw (Poland); Jouini, Mohamed, E-mail: jouini@univ-paris-diderot.f [Laboratory Interfaces, Traitements, Organisation et DYnamique des Systemes (ITODYS) UMR 7086, Universite Paris Diderot Paris 7 Batiment Lavoisier, 15 Rue Jean Antoine de Baif, 75205 Paris Cedex 13 (France); Perruchot, Christian [Laboratory Interfaces, Traitements, Organisation et DYnamique des Systemes (ITODYS) UMR 7086, Universite Paris Diderot Paris 7 Batiment Lavoisier, 15 Rue Jean Antoine de Baif, 75205 Paris Cedex 13 (France); Miecznikowski, Krzysztof; Rutkowska, Iwona A. [Department of Chemistry, University of Warsaw, Pasteura 1, 02-093 Warsaw (Poland); Kulesza, Pawel J., E-mail: pkulesza@chem.uw.edu.p [Department of Chemistry, University of Warsaw, Pasteura 1, 02-093 Warsaw (Poland)

    2011-04-01

    A comparative study describing immobilization of the Dawson type mixed addenda heteropolyanion, [P{sub 2}W{sub 17}VO{sub 62}]{sup 8-} into conducting polymer films of poly(3,4-ethylenedioxythiophene), PEDOT, and poly(2,2'-bithiophene), PBT, is reported. Electrosynthesis of these hybrid films was performed using a micellar aqueous solution of the nonionic surfactant, polyethylene glycol tert-octylphenyl ether (Triton X-100). Deposited composite films were characterised electrochemically and, on the whole, they exhibited fast electron transfer (ET) properties and relatively high stability towards continuous potential cycling in acidic media. In particular, PEDOT composite showed relatively faster ET properties in comparison to PBT composite. Their permeability was investigated in the presence of cationic and anionic redox probes. Our results implied good mediating capabilities of the [P{sub 2}W{sub 17}V{sup 4+}O{sub 62}]{sup 8-} anion (within the [P{sub 2}W{sub 17}V{sup 4+}O{sub 62}]{sup 8-}-PEDOT hybrid film) towards the iron (III) reduction. The specific electrocatalytic (reductive) capabilities of hybrid films were also studied by probing the reduction of bromate. The films were further characterised by X-ray photoelectron spectroscopy to establish their interfacial elemental composition. Moreover, their surface morphology was imaged by atomic force microscopy and scanning electron microscopy. Results have shown that physicochemical properties of the investigated hybrid films were affected by polymer hydrophobicity.

  17. Application of biofiltration system on AOC removal: Column and field studies

    Energy Technology Data Exchange (ETDEWEB)

    Chien, C.C.; Kao, C.M.; Chen, C.W.; Dong, C.D.; Wu, C.Y. [National Sun Yat Sen University, Kaohsiung (Taiwan). Inst. for Environmental Engineering

    2008-04-15

    The Cheng-Ching Lake Water Treatment Plant (CCLWTP) is the main supplier of domestic water for the Greater Kaohsiung area, the second largest metropolis in Taiwan. Biological activated carbon (BAC) filtration is one of the major treatment processes in CCLWTP. The objectives of this study were to evaluate the effectiveness of BAC filtration on water treatment in the studied advanced water treatment plant and its capability on pollutants (e.g., AOC (assimilable organic carbon) removal. In this study, water samples from each treatment process of CCLWTP were collected and analyzed periodically to assess the variations in concentrations of AOC and other water quality indicators after each treatment unit. Moreover, the efficiency of biofiltration process using granular activated carbon (GAC) and anthracite as the fillers was also evaluated through a column experiment. Results show that the removal efficiencies for AOC, bromide, bromate, and iron are 86% 100%, 17%, and 30% after the BAC filter bed, respectively. This indicates that BAC filtration plays an important role in pollutant removal. Results of column study show that the AOC removal efficiencies in the GAC and anthracite columns are 60% and 17%, respectively. Microbial colonization on GAC and anthracite were detected via the observation of scanning electron microscopic images. The observed microorganisms included bacteria (rods, cocci, and filamentous bacteria), fungi, and protozoa.

  18. Electrochemistry and electrocatalysis of polyoxometalate-ordered mesoporous carbon modified electrode

    Energy Technology Data Exchange (ETDEWEB)

    Zhou Ming [Faculty of Chemistry, Northeast Normal University, Changchun 130024 (China); Guo Liping [Faculty of Chemistry, Northeast Normal University, Changchun 130024 (China)]. E-mail: guolp078@nenu.edu.cn; Lin Fanyun [Faculty of Chemistry, Northeast Normal University, Changchun 130024 (China); Liu Haixia [Faculty of Chemistry, Northeast Normal University, Changchun 130024 (China)

    2007-03-21

    In this work, we have developed a convenient and efficient method for the functionalization of ordered mesoporous carbon (OMC) using polyoxometalate H{sub 6}P{sub 2}Mo{sub 18}O{sub 62}.xH{sub 2}O (P{sub 2}Mo{sub 18}). By the method, glassy carbon (GC) electrode modified with P{sub 2}Mo{sub 18} which was immobilized on the channel surface of OMC was prepared and characterized for the first time. The large specific surface area and porous structure of the modified OMC particles result in high heteropolyacid loading, and the P{sub 2}Mo{sub 18} entrapped in this order matrix is stable. Fourier transform infrared spectroscopy (FTIR), nitrogen adsorption-desorption isotherm and X-ray diffraction (XRD) were employed to give insight into the intermolecular interaction between OMC and P{sub 2}Mo{sub 18}. The electrochemical behavior of the modified electrode was studied in detail, including pH-dependence, stability and so on. The cyclic voltammetry (CV) and amperometry studies demonstrated that P{sub 2}Mo{sub 18}/OMC/GC electrode has high stability, fast response and good electrocatalytic activity for the reduction of nitrite, bromate, idonate, and hydrogen peroxide. The mechanism of catalysis on P{sub 2}Mo{sub 18}/OMC/GC electrode was discussed. Moreover, the development of our approach for OMC functionalization suggests the potential applications in catalysis, molecular electronics and sensors.

  19. pH-oscillations in the bromate–sulfite reaction in semibatch and in gel-fed batch reactors

    Energy Technology Data Exchange (ETDEWEB)

    Poros, Eszter; Kurin-Csörgei, Krisztina; Szalai, István; Orbán, Miklós, E-mail: orbanm@chem.elte.hu [Department of Analytical Chemistry, Institute of Chemistry, L. Eötvös University, P.O. Box 32, H-1518 Budapest 112 (Hungary); Rábai, Gyula [Institute of Physical Chemistry, University of Debrecen, P.O. Box 7, H-4010 Debrecen (Hungary)

    2015-06-15

    The simplest bromate oxidation based pH-oscillator, the two component BrO{sub 3}{sup −}–SO{sub 3}{sup 2–} flow system was transformed to operate under semibatch and closed arrangements. The experimental preconditions of the pH-oscillations in semibatch configuration were predicted by model calculations. Using this information as guideline large amplitude (ΔpH∼3), long lasting (11–24 h) pH-oscillations accompanied with only a 20% increase of the volume in the reactor were measured when a mixture of Na{sub 2}SO{sub 3} and H{sub 2}SO{sub 4} was pumped into the solution of BrO{sub 3}{sup −} with a very low rate. Batch-like pH-oscillations, similar in amplitude and period time appeared when the sulfite supply was substituted by its dissolution from a gel layer prepared previously in the reactor in presence of high concentration of Na{sub 2}SO{sub 3}. The dissolution vs time curve and the pH-oscillations in the semibatch and closed systems were successfully simulated. Due to the simplicity in composition and in experimental technique, the semibatch and batch-like BrO{sub 3}{sup −}–SO{sub 3}{sup 2–} pH-oscillators may become superior to their CSTR (continuous flow stirred tank reactor) version in some present and future applications.

  20. Two new inorganic-organic hybrid single pendant hexadecavanadate derivatives with bifunctional electrocatalytic activities

    Energy Technology Data Exchange (ETDEWEB)

    Dong, Baoxia [Key Laboratory of Polyoxometalate Science of Ministry of Education, Faculty of Chemistry, Northeast Normal University, Changchun, Jilin 130024 (China); Peng, Jun [Key Laboratory of Polyoxometalate Science of Ministry of Education, Faculty of Chemistry, Northeast Normal University, Changchun, Jilin 130024 (China)]. E-mail: jpeng@nenu.edu.cn; Tian, Aixiang [Key Laboratory of Polyoxometalate Science of Ministry of Education, Faculty of Chemistry, Northeast Normal University, Changchun, Jilin 130024 (China); Sha, Jingquan [Key Laboratory of Polyoxometalate Science of Ministry of Education, Faculty of Chemistry, Northeast Normal University, Changchun, Jilin 130024 (China); Li, Li [Key Laboratory of Polyoxometalate Science of Ministry of Education, Faculty of Chemistry, Northeast Normal University, Changchun, Jilin 130024 (China); Liu, Hongsheng [Key Laboratory of Polyoxometalate Science of Ministry of Education, Faculty of Chemistry, Northeast Normal University, Changchun, Jilin 130024 (China)

    2007-03-01

    Two new supramolecular assembly hexadecavanadate derivatives of H{sub 2}[Cd(phen){sub 3}]{sub 2}{l_brace}[Cd(H{sub 2}O)(phen){sub 2}](V{sub 16}O{sub 38}Cl){r_brace}.2.5H{sub 2}O 1 (phen = 1,10'-phenanthroline) and H{sub 2}[Cd(bipy){sub 3}][Cd(H{sub 2}O)(bipy){sub 2}]{l_brace}[Cd(H{sub 2}O)(bipy){sub 2}](V{sub 16}O{sub 38}Cl){r_brace}.1.5H{sub 2}O 2 (bipy 2,2'-bipyridine), have been prepared under mild hydrothermal conditions and structurally characterized by IR, XPS spectra, TG analyses and single-crystal X-ray diffraction. Compounds 1 and 2 are constructed from single pendant [CdL{sub 2}] (L = phen, 1 and L = bipy, 2) modified hexadecavanadates. The hybrids 1 and 2 were used as solid bulk modifier to fabricate bulk-modified carbon paste electrodes (CPEs) (1-CPE and 2-CPE) by direct mixing. The electrochemical behaviors and electrocatalysis of 1-CPE and 2-CPE indicate bifunctional electrocatalytic activities toward both the oxidation and reduction of nitrite. Furthermore, their electrocatalytic activities toward the reduction of bromate and oxidation of ascorbic acid are also studied in 1 M H{sub 2}SO{sub 4} aqueous solutions.

  1. A Novel Kinetic Spectrophotometric Method for the Determination of Dopamine in Biological and Pharmaceutical Samples

    Directory of Open Access Journals (Sweden)

    M. Reza Shishehbore

    2013-01-01

    Full Text Available A sensitive and accurate method for quantitative determination of dopamine was introduced. The proposed method is based on inhibitory effect of dopamine on the oxidation of thionine by bromate in acidic media. The change in absorbance was followed spectrophotometrically at 601 nm. The dependence of sensitivity on the reaction variables was investigated and optimized to obtain the maximum sensitivity. Under optimum experimental conditions, calibration curve was linear over the range 0.2–103.3 μg mL−1 of dopamine. The relative standard deviations ( of 0.5, 1.0, 5.0, and 30.0 μg mL−1 of dopamine were 1.13, 1.02, 0.99, and 0.97%, respectively. The limit of detection was 0.057 μg mL−1 of dopamine. The effect of diverse species was also investigated. The developed method was successfully applied for the determination of dopamine in pharmaceutical and biological samples.

  2. Protective Effects of Extracts from Fructus rhodomyrti against Oxidative DNA Damage In Vitro and In Vivo

    Directory of Open Access Journals (Sweden)

    Yuebin Ke

    2013-01-01

    Full Text Available Objective. To evaluate the potential protective effects of extracts from Fructus rhodomyrti (FR against oxidative DNA damage using a cellular system and the antioxidant ability on potassium bromate- (KBrO3- mediated oxidative stress in rats. Methods. The effects of FR on DNA damage induced by hydrogen peroxide (H2O2 were evaluated by comet assay in primary spleen lymphocytes cultures. The effects of FR on the activities of SOD, CAT, and GPx and the levels of GSH, hydroperoxides, and 8-OHdG were determined in the plasma and tissues of rats treated with KBrO3. Results. FR was shown to effectively protect against DNA damage induced by H2O2  in vitro, and the maximum protective effect was observed when FR was diluted 20 times. Endogenous antioxidant status, namely, the activities of SOD, CAT, and GPx and the levels of GSH were significantly decreased in the plasma, the liver, and the kidney of the KBrO3-treated rats, while the pretreatment of FR prevented the decreases of these parameters. In addition, the pretreatment of FR was also able to prevent KBrO3-induced increases in the levels of hydroperoxides and 8-OHdG in the plasma, the liver, and the kidney in rats. Conclusions. Our findings suggested that FR might act as a chemopreventive agent with antioxidant properties offering effective protection against oxidative DNA damage in a concentration-dependent manner in vitro and in vivo.

  3. Photodegradation of clopyralid in TiO{sub 2} suspensions: Identification of intermediates and reaction pathways

    Energy Technology Data Exchange (ETDEWEB)

    Sojic, Daniela V., E-mail: daniela@ih.ns.ac.yu [Faculty of Sciences, Department of Chemistry, Trg D. Obradovica 3, 21000 Novi Sad (Serbia); Anderluh, Vesna B. [Faculty of Sciences, Department of Chemistry, Trg D. Obradovica 3, 21000 Novi Sad (Serbia); Orcic, Dejan Z., E-mail: orcicdejan@gmail.com [Faculty of Sciences, Department of Chemistry, Trg D. Obradovica 3, 21000 Novi Sad (Serbia); Abramovic, Biljana F., E-mail: abramovic@ih.ns.ac.yu [Faculty of Sciences, Department of Chemistry, Trg D. Obradovica 3, 21000 Novi Sad (Serbia)

    2009-08-30

    The work is concerned with the kinetics, identification of intermediates and reaction pathways of the photocatalytic degradation of the herbicide clopyralid (3,6-dichloropyridine-2-carboxylic acid) in UV illuminated aqueous suspensions of TiO{sub 2} (Degussa P25). In the investigated concentration range (0.5-3.0 mM) the photocatalytic degradation kinetics of clopyralid in the first stage of the reaction follows approximately a pseudo-first kinetic order. The highest reaction rate was observed at 4 mg mL{sup -1}of catalyst concentration, the apparent activation energy of the reaction being 7.74 kJ mol{sup -1}. The effect of the presence of hydrogen peroxide, potassium bromate, and ammonium persulfate, acting as electron acceptors along with molecular oxygen, were also studied. By studying the effect of ethanol as a hydroxyl radical scavenger it was shown that the heterogeneous catalysis takes place mainly via hydroxyl radicals. The reaction intermediates (3,6-dichloropyridin-2-ol, 3,6-dichloro hydroxypyridine-2-carboxylic acid, and 3,3',6,6'-tetrachloro-2,4'-bipyridine-2'-carboxylic acid) were identified and the kinetics of their appearance/disappearance was followed by LC-MS/MS (ESI+). Tentative photodegradation pathways were proposed and discussed.

  4. Electrochemical behavior and its electrocatalytic properties of chemically modified electrode with Keggin-type [SiNi(H{sub 2}O)W{sub 11}O{sub 39}]{sup 6-}

    Energy Technology Data Exchange (ETDEWEB)

    Chen Chuangye [College of Chemistry and Chemical engineering, Jiangxi Normal University, Nanchang 330022 (China); Song Yonghai [College of Chemistry and Chemical engineering, Jiangxi Normal University, Nanchang 330022 (China)], E-mail: yhsong@jxnu.edu.cn; Wang Li [College of Chemistry and Chemical engineering, Jiangxi Normal University, Nanchang 330022 (China)], E-mail: lwang@jxnu.edu.cn

    2009-02-01

    A monolayer of Keggin-type heteropolyanion [SiNi(H{sub 2}O)W{sub 11}O{sub 39}]{sup 6-} was fabricated by electrodepositing [SiNi(H{sub 2}O)W{sub 11}O{sub 39}]{sup 6-} on cysteamine modified gold electrode. The monolayer of [SiNi(H{sub 2}O)W{sub 11}O{sub 39}]{sup 6-} modified gold electrode was characterized by atomic force microscopy (AFM) and electrochemical method. AFM results showed the [SiNi(H{sub 2}O)W{sub 11}O{sub 39}]{sup 6-} uniformly deposited on the electrode surface and formed a porous monolayer. Cyclic voltammetry exhibited one oxidation peak and two reduction peaks in 1.0 M H{sub 2}SO{sub 4} in the potential range of -0.2 to 0.7 V. The constructed electrode could exist in a large pH (0-7.6) range and showed good catalytic activity towards the reduction of bromate anion (BrO{sub 3}{sup -}) and nitrite (NO{sub 2}{sup -}), and oxidation of ascorbic acid (AA) in acidic solution. The well catalytic active of the electrode was ascribed to the porous structure of the [SiNi(H{sub 2}O)W{sub 11}O{sub 39}]6{sup -} monolayer.

  5. Laser-induced removal of a dye C.I. Acid Red 87 using n-type WO{sub 3} semiconductor catalyst

    Energy Technology Data Exchange (ETDEWEB)

    Qamar, M. [Center of Excellence in Nanotechnology, King Fahd University of Petroleum and Minerals, KFUPM Box 741, Dhahran 31261 (Saudi Arabia); Gondal, M.A., E-mail: magondal@kfupm.edu.sa [Center of Excellence in Nanotechnology, King Fahd University of Petroleum and Minerals, KFUPM Box 741, Dhahran 31261 (Saudi Arabia); Laser Research Laboratory, Physics Department, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Hayat, K. [Chemistry Department, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Yamani, Z.H. [Center of Excellence in Nanotechnology, King Fahd University of Petroleum and Minerals, KFUPM Box 741, Dhahran 31261 (Saudi Arabia); Laser Research Laboratory, Physics Department, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Al-Hooshani, K. [Center of Excellence in Nanotechnology, King Fahd University of Petroleum and Minerals, KFUPM Box 741, Dhahran 31261 (Saudi Arabia); Chemistry Department, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia)

    2009-10-30

    Water contamination by organic substances such as dyes is of great concern worldwide due to their utilization in many industrial processes and environmental concerns. To cater the needs for waste water treatment polluted with organic dyes, laser-induced photocatalytic process was investigated for removal of a dye derivative namely Acid Red 87 using n-type WO{sub 3} semiconductor catalyst. The degradation was investigated in aqueous suspensions of tungsten oxide under different experimental conditions using laser instead of conventional UV lamp as an irradiation source. The degradation process was monitored by measuring the change in dye concentration as a function of laser irradiation time by employing UV spectroscopic analysis. The degradation of dye was studied by varying different parameters such as laser energy, reaction pH, substrate concentration, catalyst concentration, and in the presence of electron acceptors such as hydrogen peroxide (H{sub 2}O{sub 2}), and potassium bromate (KBrO{sub 3}). The degradation rates were found to be strongly dependent on all the above-mentioned parameters. Our experimental results revealed that the dye degradation process was very fast (within few minutes) under laser irradiation as compared to conventional setups using broad spectral lamps (hours or days) and this laser-induced photocatalytic degradation method could be an effective means to eliminate the pollutants present in liquid phase. The experience gained through this study could be beneficial for treatment of waste water contaminated with organic dyes and other organic pollutants.

  6. Capacitive behavior of nanostructured MnO{sub 2} prepared by sonochemistry method

    Energy Technology Data Exchange (ETDEWEB)

    Zolfaghari, Alireza [Chemistry and Chemical Engineering Research Center of Iran (Iran); Ataherian, Fatemeh; Ghaemi, Mehdi; Gholami, Ameneh [Department of Chemistry, Science Faculty, Tarbiat Modares University, Tehran (Iran)

    2007-02-10

    Nanostructured manganese dioxide has been successfully prepared by a sonochemical method from an aqueous solution of potassium bromate and manganese sulfate. Changing the proportions of reagents leads either to {gamma}- or layered structures of MnO{sub 2}. The capacitive characteristics of the samples were systematically investigated in aqueous electrolytes through means of cyclic voltammetry and chronopotentiometry methods. The electrochemical properties of MnO{sub 2} were strongly affected by the pH of electrolyte employed and this material exhibited ideally capacitive behavior in 0.5 M aqueous Na{sub 2}SO{sub 4} solution. A maximum specific capacitance of 344 F g{sup -1} was obtained for the layered structure determined via cyclic voltammetry at a scan rate of 5 mV s{sup -1} in 0.5 M aqueous Na{sub 2}SO{sub 4} solution at pH 3.3. Excellent electrochemical reversibility of the materials was also demonstrated. Layered structure MnO{sub 2} showed higher energy density at high power density than the {gamma}-structure material. Impedance spectroscopy studies revealed that charge transfer resistance of the {gamma}-structure oxide has higher value than that of the layered structure. (author)

  7. [Substitution of ascorbic acid for potassium bromide in the making of French bread].

    Science.gov (United States)

    Corrales, X; Guerra, M; Granito, M; Ferris, J

    1993-09-01

    The potassium bromate (PB) is the flour improving additive for bread making, most widely used in Venezuela. This additive has been reported to have hazardous effects. For this reason it has been forbidden in various countries. In order to find a substitute for PB, the feasibility of using ascorbic acid (AA) in bread making flours was considered. Flours with 80, 40 and 20 ppm of AA were tested and contrasted with an experimental and industrial flour with 80 ppm of PB, maximum quantity allowed by the Venezuelan Legislation. The effect of these additives was evaluated on French bread, of high consumption in our country. It was found that the bread prepared using the flour containing 20 ppm of AA did not present significant differences from those made out of the pattern flour, concerning their organoleptic and physico-chemical properties. It was demonstrated that it is technically feasible to replaced 80 ppm of PB for 20 ppm of AA in the flours, without affecting the bread acceptability.

  8. Oxidative Stress in the Carcinogenicity of Chemical Carcinogens

    Energy Technology Data Exchange (ETDEWEB)

    Kakehashi, Anna; Wei, Min [Department of Pathology, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-Ku, Osaka 545-8585 (Japan); Fukushima, Shoji [Japan Bioassay Research Center, Japan Industrial Safety and Health Association, 2445 Hirasawa, Hadano, Kanagawa 257-0015 (Japan); Wanibuchi, Hideki, E-mail: wani@med.osaka-cu.ac.jp [Department of Pathology, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-Ku, Osaka 545-8585 (Japan)

    2013-10-28

    This review highlights several in vivo studies utilizing non-genotoxic and genotoxic chemical carcinogens, and the mechanisms of their high and low dose carcinogenicities with respect to formation of oxidative stress. Here, we survey the examples and discuss possible mechanisms of hormetic effects with cytochrome P{sub 450} inducers, such as phenobarbital, α-benzene hexachloride and 1,1-bis(p-chlorophenyl)-2,2,2-trichloroethane. Epigenetic processes differentially can be affected by agents that impinge on oxidative DNA damage, repair, apoptosis, cell proliferation, intracellular communication and cell signaling. Non-genotoxic carcinogens may target nuclear receptors and induce post-translational modifications at the protein level, thereby impacting on the stability or activity of key regulatory proteins, including oncoproteins and tumor suppressor proteins. We further discuss role of oxidative stress focusing on the low dose carcinogenicities of several genotoxic carcinogens such as a hepatocarcinogen contained in seared fish and meat, 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline, arsenic and its metabolites, and the kidney carcinogen potassium bromate.

  9. Removal of BrO₃⁻ from drinking water samples using newly developed agricultural waste-based activated carbon and its determination by ultra-performance liquid chromatography-mass spectrometry.

    Science.gov (United States)

    Naushad, Mu; Khan, Mohammad R; ALOthman, Zeid A; AlSohaimi, Ibrahim; Rodriguez-Reinoso, Francisco; Turki, Turki M; Ali, Rahmat

    2015-10-01

    Activated carbon was prepared from date pits via chemical activation with H3PO4. The effects of activating agent concentration and activation temperature on the yield and surface area were studied. The optimal activated carbon was prepared at 450 °C using 55 % H3PO4. The prepared activated carbon was characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, thermogravimetric-differential thermal analysis, and Brunauer, Emmett, and Teller (BET) surface area. The prepared date pit-based activated carbon (DAC) was used for the removal of bromate (BrO3 (-)). The concentration of BrO3 (-) was determined by ultra-performance liquid chromatography-mass tandem spectrometry (UPLC-MS/MS). The experimental equilibrium data for BrO3 (-) adsorption onto DAC was well fitted to the Langmuir isotherm model and showed maximum monolayer adsorption capacity of 25.64 mg g(-1). The adsorption kinetics of BrO3 (-) adsorption was very well represented by the pseudo-first-order equation. The analytical application of DAC for the analysis of real water samples was studied with very promising results.

  10. The control of disinfection byproducts and their precursors in biologically active filtration processes.

    Science.gov (United States)

    Liu, Chao; Olivares, Christopher I; Pinto, Ameet J; Lauderdale, Chance V; Brown, Jess; Selbes, Meric; Karanfil, Tanju

    2017-11-01

    While disinfection provides hygienically safe drinking water, the disinfectants react with inorganic or organic precursors, leading to the formation of harmful disinfection byproducts (DBPs). Biological filtration is a process in which an otherwise conventional granular filter is designed to remove not only fine particulates but also dissolved organic matters (e.g., DBP precursors) through microbially mediated degradation. Recently, applications of biofiltration in drinking water treatment have increased significantly. This review summarizes the effectiveness of biofiltration in removing DBPs and their precursors and identifies potential factors in biofilters that may control the removal or contribute to formation of DBP and their precursors during drinking water treatment. Biofiltration can remove a fraction of the precursors of halogenated DBPs (trihalomethanes, haloacetic acids, haloketones, haloaldehydes, haloacetonitriles, haloacetamides, and halonitromethanes), while also demonstrating capability in removing bromate and halogenated DBPs, except for trihalomethanes. However, the effectiveness of biofiltration mediated removal of nitrosamine and its precursors appears to be variable. An increase in nitrosamine precursors after biofiltration was ascribed to the biomass sloughing off from media or direct nitrosamine formation in the biofilter under certain denitrifying conditions. Operating parameters, such as pre-ozonation, media type, empty bed contact time, backwashing, temperature, and nutrient addition may be optimized to control the regulated DBPs in the biofilter effluent while minimizing the formation of unregulated emerging DBPs. While summarizing the state of knowledge of biofiltration mediated control of DBPs, this review also identifies several knowledge gaps to highlight future research topics of interest. Copyright © 2017 Elsevier Ltd. All rights reserved.

  11. Dicationic imidazolium ionic liquid modified silica as a novel reversed-phase/anion-exchange mixed-mode stationary phase for high-performance liquid chromatography.

    Science.gov (United States)

    Sun, Min; Feng, Juanjuan; Wang, Xiaojiao; Duan, Huimin; Li, Leilei; Luo, Chuannan

    2014-08-01

    A dicationic imidazolium ionic liquid modified silica stationary phase was prepared and evaluated by reversed-phase/anion-exchange mixed-mode chromatography. Model compounds (polycyclic aromatic hydrocarbons and anilines) were separated well on the column by reversed-phase chromatography; inorganic anions (bromate, bromide, nitrate, iodide, and thiocyanate), and organic anions (p-aminobenzoic acid, p-anilinesulfonic acid, sodium benzoate, pathalic acid, and salicylic acid) were also separated individually by anion-exchange chromatography. Based on the multiple sites of the stationary phase, the column could separate 14 solutes containing the above series of analytes in one run. The dicationic imidazolium ionic liquid modified silica can interact with hydrophobic analytes by the hydrophobic C6 chain; it can enhance selectivity to aromatic compounds by imidazolium groups; and it also provided anion-exchange and electrostatic interactions with ionic solutes. Compared with a monocationic ionic liquid functionalized stationary phase, the new stationary phase represented enhanced selectivity owing to more interaction sites. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  12. Speciative determination of total V and dissolved inorganic vanadium species in environmental waters by catalytic–kinetic spectrophotometric method

    Directory of Open Access Journals (Sweden)

    Ramazan Gürkan

    2017-02-01

    Full Text Available A kinetic determination of V(V as a catalyst was spectrophotometrically performed by using the indicator reaction of Gallamine blue (GB+ and bromate at pH 2.0. The reaction was followed by measuring absorbance change for a fixed-time of 3 min at 537 nm. The variables such as reagent concentration, pH, buffer concentration, ionic strength and temperature were optimized to improve the selectivity and sensitivity. Under the optimized conditions, the determination of V(V was performed in the range 1–100 μg L−1 with limits of detection and quantification of 0.31 and 0.94 μg L−1. The developed kinetic method is sufficiently sensitive, selective and simple. It was successfully applied to the speciative determination of total V and inorganic dissolved vanadium species, V(V and V(IV in environmental water samples. The oxidizing property of permanganate is used to differentiate between V(IV and V(V species. The V(IV content was found by subtracting the V(V content from those of total V. The recovery is above 95% for V(V spiked samples. Additionally, the accuracy was validated by analysis of a certified water sample, CRM TMDA-53.3, and the results were in good agreement with the certified value.

  13. Remedial Process Optimization and Green In-Situ Ozone Sparging for Treatment of Groundwater Impacted with Petroleum Hydrocarbons

    Science.gov (United States)

    Leu, J.

    2012-12-01

    A former natural gas processing station is impacted with TPH and BTEX in groundwater. Air sparging and soil vapor extraction (AS/AVE) remediation systems had previously been operated at the site. Currently, a groundwater extraction and treatment system is operated to remove the chemicals of concern (COC) and contain the groundwater plume from migrating offsite. A remedial process optimization (RPO) was conducted to evaluate the effectiveness of historic and current remedial activities and recommend an approach to optimize the remedial activities. The RPO concluded that both the AS/SVE system and the groundwater extraction system have reached the practical limits of COC mass removal and COC concentration reduction. The RPO recommended an in-situ chemical oxidation (ISCO) study to evaluate the best ISCO oxidant and approach. An ISCO bench test was conducted to evaluate COC removal efficiency and secondary impacts to recommend an application dosage. Ozone was selected among four oxidants based on implementability, effectiveness, safety, and media impacts. The bench test concluded that ozone demand was 8 to 12 mg ozone/mg TPH and secondary groundwater by-products of ISCO include hexavalent chromium and bromate. The pH also increased moderately during ozone sparging and the TDS increased by approximately 20% after 48 hours of ozone treatment. Prior to the ISCO pilot study, a capture zone analysis (CZA) was conducted to ensure containment of the injected oxidant within the existing groundwater extraction system. The CZA was conducted through a groundwater flow modeling using MODFLOW. The model indicated that 85%, 90%, and 95% of an injected oxidant could be captured when a well pair is injecting and extracting at 2, 5, and 10 gallons per minute, respectively. An ISCO pilot test using ozone was conducted to evaluate operation parameters for ozone delivery. The ozone sparging system consisted of an ozone generator capable of delivering 6 lbs/day ozone through two ozone

  14. Health effects of disinfection by-products in chlorinated swimming pools.

    Science.gov (United States)

    Florentin, Arnaud; Hautemanière, Alexis; Hartemann, Philippe

    2011-11-01

    Increased attendance at swimming pools is correlated with higher input of organic and minerals pollutants introduced by swimmers in the swimming pool water. In most swimming pools, microbiological control is performed by disinfection with the addition of chlorine. Chlorine is now well-known to lead to the formation of many disinfection by-products (DBPs) including trihalomethanes and chloramines. The hypothesis of a link between the presence of eye and skin irritation syndromes in swimmers and contact with swimming pool water treated with chlorine was initially proposed by Mood (1953). During recent decades many epidemiological studies have described the importance of DBPs generated with natural or imported organic matter present in water. Many of these DBPs are suspected to be toxic or even carcinogenic. Trihalomethanes and haloacetic acid families are the most studied but others DBPs, like chloral hydrate, haloacetonitriles, N-nitrosodimethylamine and the bromate ion, are emerging compounds of interest. Epidemiological data about the risk of cancer are still controversial. However, numerous publications highlight a toxic risk especially the risk of allergy and respiratory symptoms for babies and elite swimmers. The few publications dedicated to risk assessment do not suggest increased risk, other than for elite swimmers. These publications are likely to underestimate the risk associated with DBPs because of the lack of data in the literature precludes the calculation of risk associated with certain compounds or certain pathways. Thus for regulations, the need to take into account the risks associated with disinfection by-products is now important without forgetting the need of the control of microbiological hazards in swimming pools. Copyright © 2011 Elsevier GmbH. All rights reserved.

  15. Influence of 300°C thermal conversion of Fe-Ce hydrous oxides prepared by hydrothermal precipitation on the adsorptive performance of five anions: Insights from EXAFS/XANES, XRD and FTIR (companion paper).

    Science.gov (United States)

    Chubar, Natalia; Gerda, Vasyl; Banerjee, Dipanjan

    2017-04-01

    In this work, we report atomic-scale reconstruction processes in Fe-Ce oxide-based composites (hydrothermally precipitated at Fe-to-Ce dosage ratios of 1:0, 2:1, 1:1, 1:2, and 0:1), upon treatment at 300°C. The structural changes are correlated with the adsorptive removal of arsenate, phosphate, fluoride, bromide, and bromate. The presence of the carbonate-based Ce-component and surface sulfate in precursor samples creates favorable conditions for phase transformation, resulting in the formation of novel (unknown) layered compounds of Fe and Ce. These compounds are of the layered double hydroxide type, with sulfate in the interlayer space. In spite of general awareness of the importance of surface area in adsorptive removal, the increase in surface area upon thermal treatment did not increase adsorption of the studied anions. However, EXAFS simulations and the adsorption tests provided evidence of regularities between local structures of Fe in composites obtained at 80 and 300°C and adsorption performance of most studied anions. The best adsorption of tetrahedral anions was demonstrated by samples whose simulated outer Fe shells resulted from oscillations from both O and Fe atoms. In contrast, the loss of extended x-ray absorption fine structure was correlated with the decrease of adsorptive removal. Both Fe K-edge and Ce L3 -edge EXAFS suggested the formation of solid solutions. For the first time, the utilization of extended x-ray absorption fine structure is suggested as a methodological approach (first expressed in the companion paper) to estimate the surface reactivity of inorganic materials intended for use as anion exchange adsorbents. Copyright © 2016 Elsevier Inc. All rights reserved.

  16. Conducting polymer-based hybrid assemblies for electrochemical sensing: a materials science perspective.

    Science.gov (United States)

    Janáky, Csaba; Visy, Csaba

    2013-04-01

    In this topical review, progress achieved in amperometric sensing of different analytes over conducting polymer-based hybrid electrocatalysts is summarized. We report a variety of synthetic methods and the resulting hybrid assemblies, with the effectiveness of such strategies, for designing conjugated polymer-based hybrids as robust sensors for amperometric detection. Beyond incorporation of metal nanoparticles, metal-oxide and non-oxide semiconductors, carbon-based nanomaterials (nanotubes, graphene, and graphene oxide), and special dopant ions are also discussed. Moreover, some particularly interesting miscellaneous approaches, for example photo-amperometric sensing or use of overoxidized polymers, are also emphasized. Determination of dissolved gases (for example O2, NO, and NO2), ions (sulfite, nitrite, nitrate, chlorate, bromate, and iodate) and smaller and larger molecules (for example H2O2, ascorbic acid (AA), dopamine (DA), urea (UA), amino acids, hydrazine, NADH, serotonin, and epinephrine) is discussed. These achievements are reviewed from the materials perspective, addressing both synthetic and electrocatalytic aspects of the polymer-based modified electrodes. Beyond simple or more sophisticated mixing, a wide range of methods of preparation is presented, including chemical (one-pot polymerization, impregnation), electrochemical (co-deposition, doping type inclusion, etc.) and combined strategies. Classification of such synthetic routes is also included. However, it is important to note that we omit studies in which conducting polymers alone were used for determination of different species. Furthermore, because excellent reviews--cited in this work also--are available on immobilization of biomolecules (for example enzymes) for biosensing purposes, this topic, also, is excluded.

  17. Zirconium-based metal organic frameworks: Highly selective adsorbents for removal of phosphate from water and urine

    Energy Technology Data Exchange (ETDEWEB)

    Lin, Kun-Yi Andrew, E-mail: linky@nchu.edu.tw [Department of Environmental Engineering, National Chung Hsing University, 250 Kuo-Kuang Road, Taichung, Taiwan (China); Chen, Shen-Yi [Department of Environmental Engineering, National Chung Hsing University, 250 Kuo-Kuang Road, Taichung, Taiwan (China); Jochems, Andrew P. [New Mexico Bureau of Geology & Mineral Resources and New Mexico Institute of Mining & Technology, Socorro, NM (United States)

    2015-06-15

    Phosphate is one of the most concerning compounds in wastewater streams and a main nutrient that causes eutrophication. To eliminate the phosphate pollution, Metal Organic Frameworks (MOFs) are proposed in this study as adsorbents to remove phosphate from water. The zirconium-based MOF, UiO-66, was selected as representative MOF given its exceptional stability in water. To investigate the effect of an amine functional group, UiO-66-NH2 was also prepared using an amine-substituted ligand. The adsorption kinetics and isotherm reveal that UiO-66-NH2 exhibited higher adsorption capacities than UiO-66 possibly due to the amine group. However, the interaction between phosphate and zirconium sites of UiO MOFs might be the primary factor accounting for the phosphate adsorption to UiO MOFs. UiO MOFs also exhibited a high selectivity towards phosphate over other anions such as bromate, nitrite and nitrate. Furthermore, UiO MOFs were found to adsorb phosphate and to completely remove diluted phosphate in urine. We also found that UiO MOFs could be easily regenerated and re-used for phosphate adsorption. These findings suggest that UiO MOFs can be effective and selective adsorbents to remove phosphate from water as well as urine. - Highlights: • UiO-66 as the first type of MOFs was used to remove phosphate from water and urine. • The amine group in UiO MOFs was found to enhance the phosphate adsorption. • UiO-66 exhibited a high adsorption selectivity towards phosphate over other anions. • UiO-66 could be easily regenerated and re-used with 85% regeneration efficiency.

  18. Influence of 300°C thermal conversion of Fe-Ce hydrous oxides prepared by hydrothermal precipitation on the adsorptive performance of five anions: Insights from EXAFS/XANES, XRD and FTIR (companion paper)

    KAUST Repository

    Chubar, Natalia

    2016-12-07

    In this work, we report atomic-scale reconstruction processes in Fe-Ce oxide-based composites (hydrothermally precipitated at Fe-to-Ce dosage ratios of 1:0, 2:1, 1:1, 1:2, and 0:1), upon treatment at 300 °C. The structural changes are correlated with the adsorptive removal of arsenate, phosphate, fluoride, bromide, and bromate. The presence of the carbonate-based Ce-component and surface sulfate in precursor samples creates favorable conditions for phase transformation, resulting in the formation of novel (unknown) layered compounds of Fe and Ce. These compounds are of the layered double hydroxide type, with sulfate in the interlayer space. In spite of general awareness of the importance of surface area in adsorptive removal, the increase in surface area upon thermal treatment did not increase adsorption of the studied anions. However, EXAFS simulations and the adsorption tests provided evidence of regularities between local structures of Fe in composites obtained at 80 and 300 °C and adsorption performance of most studied anions. The best adsorption of tetrahedral anions was demonstrated by samples whose simulated outer Fe shells resulted from oscillations from both O and Fe atoms. In contrast, the loss of extended x-ray absorption fine structure was correlated with the decrease of adsorptive removal. Both Fe K-edge and Ce L3 -edge EXAFS suggested the formation of solid solutions. For the first time, the utilization of extended x-ray absorption fine structure is suggested as a methodological approach (first expressed in the companion paper) to estimate the surface reactivity of inorganic materials intended for use as anion exchange adsorbents.

  19. Rapid Removal of Tetrabromobisphenol A by Ozonation in Water: Oxidation Products, Reaction Pathways and Toxicity Assessment

    Science.gov (United States)

    Wang, Xinghao; Huang, Qingguo; Lu, Junhe; Wang, Liansheng; Wang, Zunyao

    2015-01-01

    Tetrabromobisphenol A (TBBPA) is one of the most widely used brominated flame retardants and has attracted more and more attention. In this work, the parent TBBPA with an initial concentration of 100 mg/L was completely removed after 6 min of ozonation at pH 8.0, and alkaline conditions favored a more rapid removal than acidic and neutral conditions. The presence of typical anions and humic acid did not significantly affect the degradation of TBBPA. The quenching test using isopropanol indicated that direct ozone oxidation played a dominant role during this process. Seventeen reaction intermediates and products were identified using an electrospray time-of-flight mass spectrometer. Notably, the generation of 2,4,6-tribromophenol was first observed in the degradation process of TBBPA. The evolution of reaction products showed that ozonation is an efficient treatment for removal of both TBBPA and intermediates. Sequential transformation of organic bromine to bromide and bromate was confirmed by ion chromatography analysis. Two primary reaction pathways that involve cleavage of central carbon atom and benzene ring cleavage concomitant with debromination were thus proposed and further justified by calculations of frontier electron densities. Furthermore, the total organic carbon data suggested a low mineralization rate, even after the complete removal of TBBPA. Meanwhile, the acute aqueous toxicity of reaction solutions to Photobacterium Phosphoreum and Daphnia magna was rapidly decreased during ozonation. In addition, no obvious difference in the attenuation of TBBPA was found by ozone oxidation using different water matrices, and the effectiveness in natural waters further demonstrates that ozonation can be adopted as a promising technique to treat TBBPA-contaminated waters. PMID:26430733

  20. Water quality, compliance, and health outcomes among utilities implementing Water Safety Plans in France and Spain.

    Science.gov (United States)

    Setty, Karen E; Kayser, Georgia L; Bowling, Michael; Enault, Jerome; Loret, Jean-Francois; Serra, Claudia Puigdomenech; Alonso, Jordi Martin; Mateu, Arnau Pla; Bartram, Jamie

    2017-05-01

    Water Safety Plans (WSPs), recommended by the World Health Organization since 2004, seek to proactively identify potential risks to drinking water supplies and implement preventive barriers that improve safety. To evaluate the outcomes of WSP application in large drinking water systems in France and Spain, we undertook analysis of water quality and compliance indicators between 2003 and 2015, in conjunction with an observational retrospective cohort study of acute gastroenteritis incidence, before and after WSPs were implemented at five locations. Measured water quality indicators included bacteria (E. coli, fecal streptococci, total coliform, heterotrophic plate count), disinfectants (residual free and total chlorine), disinfection by-products (trihalomethanes, bromate), aluminum, pH, turbidity, and total organic carbon, comprising about 240K manual samples and 1.2M automated sensor readings. We used multiple, Poisson, or Tobit regression models to evaluate water quality before and after the WSP intervention. The compliance assessment analyzed exceedances of regulated, recommended, or operational water quality thresholds using chi-squared or Fisher's exact tests. Poisson regression was used to examine acute gastroenteritis incidence rates in WSP-affected drinking water service areas relative to a comparison area. Implementation of a WSP generally resulted in unchanged or improved water quality, while compliance improved at most locations. Evidence for reduced acute gastroenteritis incidence following WSP implementation was found at only one of the three locations examined. Outcomes of WSPs should be expected to vary across large water utilities in developed nations, as the intervention itself is adapted to the needs of each location. The approach may translate to diverse water quality, compliance, and health outcomes. Copyright © 2017 Elsevier GmbH. All rights reserved.

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

    Science.gov (United States)

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

    2012-05-04

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

  2. Utilization of a Green Brominating Agent for the Spectrophotometric Determination of Pipazethate HCl in Pure Form and Pharmaceutical Preparations

    Directory of Open Access Journals (Sweden)

    Ayman A. Gouda

    2013-01-01

    Full Text Available Five simple, accurate, and sensitive spectrophotometric methods (A–E have been described for the indirect assay of pipazethate HCl (PZT either in pure form or in pharmaceutical preparations. The proposed methods are based on the bromination of pipazethate HCl with a solution of excess bromate-bromide mixture in hydrochloric acid medium and subsequent estimation of the residual bromine by different reaction schemes. In the first three methods (A–C, the determination of the residual bromine is based on its ability to bleach the color of methyl orange, indigo carmine, or thymol blue dyes and measuring the absorbance at 520, 610, and 550 nm for methods A, B, and C, respectively. Methods D and E involves treating the unreacted bromine with a measured excess of iron(II, and the remaining iron(II is complexed with 1,10-phenanthroline, and the increase in absorbance is measured at 510 nm for method D and the resulting iron(III is complexed with thiocyanate and the absorbance is measured at 480 nm for method E. The different experimental parameters affecting the development and stability of the color are carefully studied and optimized. Regression analysis of the Beer-Lambert plots showed good correlation in the concentration ranges of 0.5–8.0 μg . The apparent molar absorptivity, Sandell's sensitivity, detection and quantitation limits were evaluated. The proposed methods have been applied and validated successfully for the analysis of the drug in its pure form and pharmaceutical formulations with mean recoveries of 99.94%–100.15% and relative standard deviation ≤1.53. No interference was observed from a common pharmaceutical adjuvant. Statistical comparison of the results with the reference method shows excellent agreement and indicates no significant difference in accuracy and precision.

  3. Degradation of acid red 97 dye in aqueous medium using wet oxidation and electro-Fenton techniques.

    Science.gov (United States)

    Kayan, Berkant; Gözmen, Belgin; Demirel, Muhammet; Gizir, A Murat

    2010-05-15

    Degradation of the acid red 97 dye using wet oxidation, by different oxidants, and electro-Fenton systems was investigated in this study. The oxidation effect of different oxidants such as molecular oxygen, periodate, persulfate, bromate, and hydrogen peroxide in wet oxidation system was compared. Mineralization of AR97 with periodate appeared more effective when compared with that of the other oxidants at equal initial concentration. When 5 mM of periodate was used, at the first minute of the oxidative treatment, the decolorization percentage of AR97 solution at 150 and 200 degrees C reached 88 and 98%, respectively. The total organic carbon removal efficiency at these temperatures also reached 60 and 80%. The degradation of AR97 was also studied by electro-Fenton process. The optimal current value and Fe(2+) concentration were found to be 300 mA and 0.2 mM, respectively. The results showed that electro-Fenton process can lead to 70 and 95% mineralization of the dye solution after 3 and 5h giving carboxylic acids and inorganic ions as final end-products before mineralization. The products obtained from degradation were identified by GC/MS as 1,2-naphthalenediol, 1,1'-biphenyl-4-amino-4-ol, 2-naphthalenol diazonium, 2-naphthalenol, 2,3-dihydroxy-1,4-naphthalenedion, phthalic anhydride, 1,2-benzenedicarboxylic acid, phthaldehyde, 3-hydroxy-1,2-benzenedicarboxylic acid, 4-amino-benzoic acid, and 2-formyl-benzoic acid. Copyright (c) 2009 Elsevier B.V. All rights reserved.

  4. Electrocatalysis of the first and second kind: Theoretical and experimental study in conditions of square-wave voltammetry

    Energy Technology Data Exchange (ETDEWEB)

    Mirceski, Valentin, E-mail: valentin@pmf.ukim.m [Institutes of Chemistry, Faculty of Natural Sciences and Mathematics, ' Ss Cyril and Methodius' University, Arhimedova 5, P.O. Box 162, 1000 Skopje (Macedonia, The Former Yugoslav Republic of); Bobrowski, Andrzej; Zarebski, Jerzy [Department of Building Materials Technology, Faculty of Materials Science and Ceramics, AGH - University of Science and Technology, Al Mickiewicza 30, 30-059 Krakow (Poland); Spasovski, Filip [Institutes of Chemistry, Faculty of Natural Sciences and Mathematics, ' Ss Cyril and Methodius' University, Arhimedova 5, P.O. Box 162, 1000 Skopje (Macedonia, The Former Yugoslav Republic of)

    2010-12-01

    A comparative analysis of two common electrocatalytic mechanisms in conditions of square-wave voltammetry (SWV) is presented from both theoretical and experimental points of view. The catalytic mechanism of the first kind is represented by a simple regenerative EC' reaction scheme, where C' is a follow-up irreversible chemical reaction through which the substrate is transformed and the catalyst regenerated. The second mechanism, known as electrocatalysis of the second kind, assumes the formation of an electroactive complex YS between the catalyst Y and the electroinactive substrate S in a chemically reversible reaction, followed by an irreversible electrochemical reaction of YS that yields the catalyst Y and the final electroinactive product P. The latter mechanism is mathematically modelled based on the semi-infinite diffusion model, deriving a general solution in the form of an integral equation that may be used for any voltammetric technique. A specific recurrent formula is derived based on the step-function method, enabling the simulation of SW voltammetric experiments with a wide range of experimental parameters. The properties of the response are thoroughly analyzed in terms of the kinetics and thermodynamics of the preceding chemical reaction, as well as the kinetics of the electrode reaction. The comparative analysis of the two reaction schemes reveals that both mechanisms are rather similar, exhibiting comparable sensitivity toward the kinetics of the catalytic reaction. Theoretical analysis is experimentally illustrated with the electrocatalytic reduction of bromate and nitrite ions catalyzed by Fe(II) (catalysis of the first kind) and Co(II) ions (catalysis of the second kind), respectively.

  5. Parity violation and parity conservation in unstirred crystallization: Effect of first crystals

    Energy Technology Data Exchange (ETDEWEB)

    Szurgot, M. [Center of Mathematics and Physics, Technical University of Lodz (Poland)

    2012-02-15

    Statistics of nucleation of chiral forms was studied to establish the effect of the number of first crystals and their handedness on distributions of enantiomers. Various bimodal, trimodal and unimodal distributions are obtained in unstirred crystallization, depending on the number of initial crystals and growth conditions. The binomial distribution satisfactorily describes experimental distributions of enantiomeric excess and may be used to predict distributions and probabilities of nucleation of enantiomers. The first nucleated crystals determine the handedness of secondary crystals, and number of initial crystals governs statistics of chiral nucleation. According to the binomial distribution if single crystals nucleate as the first, the bimodal distributions result with D and L peaks. If LD, LL, and DD pairs are nucleated as first, trimodal distributions with D, R, and L peaks are created, and if groups of crystals of various handedness nucleate as the first the unimodal distributions of enantiomeric excess with racemate R peaks are formed. Chiral nucleation experiments on sodium bromate were the basis for the theoretical considerations and verifications of predictions resulting from binomial distributions on probabilities of the creation of L and D crystals, and racemates, and the presence of D, L, and R peaks in the distributions. Growth conditions affect the number of the first crystals and effectiveness of cloning, and as a result, the distributions of enantiomers. Formation of pure enantiomers and/or racemates proves that the conservation of chiral symmetry, and the breakage of chiral symmetry can occur in unstirred crystallization. (copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  6. Stability of high molecular fracgels under HTHP conditions in gas wells; Stabilitaet von hochmolekularen Fracfluiden unter HTHP-Bedingungen in Gasbohrungen

    Energy Technology Data Exchange (ETDEWEB)

    Kulicke, W.M. [Hamburg Univ. (Germany). Inst. fuer Technische und Makromolekulare Chemie

    2009-07-15

    Previous experience in frac operation showed that in many cases fracgel recovery is incomplete. This leads to a decreased productivity of the stimulated well. One assumed reason is an insufficient degradation of the fracgel due to a decrease in the effectiveness of the added breaker induced by interactions with added production chemicals. It was the purpose of this project to investigate the effectiveness of breakers for degradation of high molecular guar-based fracgels in the presence of selected production chemicals in low pH, high temperature, high pressure (HTHP)- environments. The present work covers the polymer analytical characterization of basic components for fracgel production and the synthesis of a reference fracgel with a comparable property profile of a field product. The method which was developed to investigate the influence of breakers and production chemicals on the properties of the reference fracgel and its degradation, accounts for the fracgel strength, the absolute molar mass distribution of soluble and the fraction of insoluble residues. In the temperature range of 120 C to 150 C, thermal fracgel degradation is pronounced. Ammonium peroxodisulfate (APS) is the most effective investigated breaker. Compared to APS, sodium bromate shows a significantly lower breaker activity. The temperature-stabilizing agend sodium thiosulfate decelerates fracgel degradation and reduces the effectiveness of APS without annihilating it. Above 90 C, with increasing degradation time and temperature, a part of the deployed polymer precipitates and forms a water-insoluble residue. At 150 C, its fraction increases up to 30% after 48 h. High concentrations of electrolytes favour the formation of insoluble residue. A time-dependant minimum value of the percentage of insoluble residue occurs. It can be influenced by addition of sodium thiosulfate. (orig.)

  7. Bisphenol a promotes cell survival following oxidative DNA damage in mouse fibroblasts.

    Directory of Open Access Journals (Sweden)

    Natalie R Gassman

    Full Text Available Bisphenol A (BPA is a biologically active industrial chemical used in production of consumer products. BPA has become a target of intense public scrutiny following concerns about its association with human diseases such as obesity, diabetes, reproductive disorders, and cancer. Recent studies link BPA with the generation of reactive oxygen species, and base excision repair (BER is responsible for removing oxidatively induced DNA lesions. Yet, the relationship between BPA and BER has yet to be examined. Further, the ubiquitous nature of BPA allows continuous exposure of the human genome concurrent with the normal endogenous and exogenous insults to the genome, and this co-exposure may impact the DNA damage response and repair. To determine the effect of BPA exposure on base excision repair of oxidatively induced DNA damage, cells compromised in double-strand break repair were treated with BPA alone or co-exposed with either potassium bromate (KBrO3 or laser irradiation as oxidative damaging agents. In experiments with KBrO3, co-treatment with BPA partially reversed the KBrO3-induced cytotoxicity observed in these cells, and this was coincident with an increase in guanine base lesions in genomic DNA. The improvement in cell survival and the increase in oxidatively induced DNA base lesions were reminiscent of previous results with alkyl adenine DNA glycosylase-deficient cells, suggesting that BPA may prevent initiation of repair of oxidized base lesions. With laser irradiation-induced DNA damage, treatment with BPA suppressed DNA repair as revealed by several indicators. These results are consistent with the hypothesis that BPA can induce a suppression of oxidized base lesion DNA repair by the base excision repair pathway.

  8. Determination of acrylamide in Chinese traditional carbohydrate-rich foods using gas chromatography with micro-electron capture detector and isotope dilution liquid chromatography combined with electrospray ionization tandem mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Zhang Yu [Department of Food Science and Nutrition, College of Biosystems Engineering and Food Science, Zhejiang University, Hangzhou 310029, Zhejiang Province (China); Ren Yiping [Zhejiang Provincial Center for Disease Prevention and Control, Hangzhou 310009, Zhejiang Province (China); Zhao Hangmei [Department of Food Science and Nutrition, College of Biosystems Engineering and Food Science, Zhejiang University, Hangzhou 310029, Zhejiang Province (China); Zhang Ying [Department of Food Science and Nutrition, College of Biosystems Engineering and Food Science, Zhejiang University, Hangzhou 310029, Zhejiang Province (China)]. E-mail: y_zhang@zju.edu.cn

    2007-02-19

    The present study developed two analytical methods for quantification of acrylamide in complex food matrixes, such as Chinese traditional carbohydrate-rich foods. One is based on derivatization with potassium bromate and potassium bromide without clean-up prior to gas chromatography with micro-electron capture detector (GC-MECD). Alternatively, the underivatized acrylamide was detected by high-performance liquid chromatography coupled to quadrupole tandem mass spectrometry (HPLC-MS/MS) in the positive electrospray ionization mode. For both methods, the Chinese carbohydrate-rich samples were homogenized, defatted with petroleum ether and extracted with aqueous solution of sodium chloride. Recovery rates for acrylamide from spiked Chinese style foods with the spiking level of 50, 500 and 1000 {mu}g kg{sup -1} were in the range of 79-93% for the GC-MECD including derivatization and 84-97% for the HPLC-MS/MS method. Typical quantification limits of the HPLC-MSMS method were 4 {mu}g kg{sup -1} for acrylamide. The GC-MECD method achieved quantification limits of 10 {mu}g kg{sup -1} in Chinese style foods. Thirty-eight Chinese traditional foods purchased from different manufacturers were analyzed and compared with four Western style foods. Acrylamide contaminant was found in all of samples at the concentration up to 771.1 and 734.5 {mu}g kg{sup -1} detected by the GC and HPLC method, respectively. The concentrations determined with the two different quantitative methods corresponded well with each other. A convenient and fast pretreatment procedure will be optimized in order to satisfy further investigation of hundreds of samples.

  9. Electrochemical functionalization of vertically aligned carbon nanotube arrays with molybdenum oxides for the development of a surface-charge-controlled sensor

    Energy Technology Data Exchange (ETDEWEB)

    Ye, J-S [Department of Biological Sciences, National University of Singapore, 14 Science Drive 4, 117543, Singapore (Singapore); Wen Ying [Department of Chemistry, National University of Singapore, 3 Science Drive 3, 117543, Singapore (Singapore); Zhang, W-D [Nano Science Research Center, College of Chemistry, South China University of Technology, Guangzhou 510640 (China); Cui, H F [Department of Biological Sciences, National University of Singapore, 14 Science Drive 4, 117543, Singapore (Singapore); Xu, G Q [Department of Chemistry, National University of Singapore, 3 Science Drive 3, 117543, Singapore (Singapore); Sheu, F-S [Department of Biological Sciences, National University of Singapore, 14 Science Drive 4, 117543, Singapore (Singapore)

    2006-08-14

    The modification of inorganic polymeric oxides at the surface of carbon nanotubes is of paramount importance for developing new sensors. In this study, molybdenum oxide (MoO{sub x}) film was electrodeposited on the surface of multi-walled carbon nanotubes (MWNTs) by cycling the potential between +0.20 and -0.80 V (versus 3 M KCl-Ag|AgCl) in Na{sub 2}MoO{sub 4} solution. The MoO{sub x}-modified nanotube (MoO{sub x}/MWNT) electrode displays well-defined redox transitions in 5 mM H{sub 2}SO{sub 4} or in phosphate buffer solution (PBS), which can be attributed to the reductive formation and the re-oxidation of hydrogen molybdenum oxides. X-ray photoelectron spectra (XPS) showed that the deposited MoO{sub x} films are mainly Mo{sup 6+} complexes. Both MWNT and MoO{sub x}/MWNT electrodes have ideal reversibility in 5 mM K{sub 3}[Fe(CN){sub 6}] in 1 M KCl as supporting electrolytes at all sweep rates (0.02-1.00 V s{sup -1}) by cyclic voltammetry. The negatively charged surface of MoO{sub x}/MWNTs can further attract molecular cations such as Ru(NH{sub 3}){sub 6}{sup 3+}. The MoO{sub x}/MWNT electrode exhibited electrocatalytic ability towards the reduction of bromate due to high surface area and the fast electron transfer rate of nanotubes. Thus, electrochemical modification of inorganic polymeric oxides on the carbon nanotube provides a simple method for the preparation of novel sensors.

  10. Palladium nanoparticles encapsulated in core-shell silica: A structured hydrogenation catalyst with enhanced activity for reduction of oxyanion water pollutants

    KAUST Repository

    Wang, Yin

    2014-10-03

    Noble metal nanoparticles have been applied to mediate catalytic removal of toxic oxyanions and halogenated hydrocarbons in contaminated water using H2 as a clean and sustainable reductant. However, activity loss by nanoparticle aggregation and difficulty of nanoparticle recovery are two major challenges to widespread technology adoption. Herein, we report the synthesis of a core-shell-structured catalyst with encapsulated Pd nanoparticles and its enhanced catalytic activity in reduction of bromate (BrO3-), a regulated carcinogenic oxyanion produced during drinking water disinfection process, using 1 atm H2 at room temperature. The catalyst material consists of a nonporous silica core decorated with preformed octahedral Pd nanoparticles that were further encapsulated within an ordered mesoporous silica shell (i.e., SiO2@Pd@mSiO2). Well-defined mesopores (2.3 nm) provide a physical barrier to prevent Pd nanoparticle (6 nm) movement, aggregation, and detachment from the support into water. Compared to freely suspended Pd nanoparticles and SiO2@Pd, encapsulation in the mesoporous silica shell significantly enhanced Pd catalytic activity (by a factor of 10) under circumneutral pH conditions that are most relevant to water purification applications. Mechanistic investigation of material surface properties combined with Langmuir-Hinshelwood modeling of kinetic data suggest that mesoporous silica shell enhances activity by promoting BrO3- adsorption near the Pd active sites. The dual function of the mesoporous shell, enhancing Pd catalyst activity and preventing aggregation of active nanoparticles, suggests a promising general strategy of using metal nanoparticle catalysts for water purification and related aqueous-phase applications.

  11. Sonochemical assisted synthesis MnO2/RGO nanohybrid as effective electrode material for supercapacitor.

    Science.gov (United States)

    Ghasemi, Shahram; Hosseini, Sayed Reza; Boore-Talari, Omid

    2018-01-01

    Manganese dioxide (MnO2) needle-like nanostructures are successfully synthesized by a sonochemical method from an aqueous solution of potassium bromate and manganese sulfate. Also, hybride of MnO2 nanoparticles wrapped with graphene oxide (GO) nanosheets are fabricated through an electrostatic coprecipitation procedure. With adjusting pH at 3.5, positive and negative charges are created on MnO2 and on GO, respectively which can electrostatically attract to each other and coprecipitate. Then, MnO2/GO pasted on stainless steel mesh is electrochemically reduced by applying -1.1V to obtain MnO2/RGO nanohybrid. The structure and morphology of the MnO2 and MnO2/RGO nanohybrid are examined by Raman spectroscopy, X-ray diffraction (XRD), atomic force microscopy (AFM), field emission-scanning electron microscopy (FE-SEM), energy dispersive spectroscopy (EDX), and thermal gravimetric analysis (TGA). The capacitive behaviors of MnO2 and MnO2/RGO active materials on stainless steel meshes are investigated by cyclic voltammetry (CV), galvanostatic charge/discharge test and electrochemical impedance spectroscopy (EIS) by a three-electrode experimental setup in an aqueous solution of 0.5M sodium sulfate in the potential window of 0.0-1.0V. The electrochemical investigations reveal that MnO2/RGO exhibits high specific capacitance (Cs) of 375Fg(-1) at current density of 1Ag(-1) and good cycle stability (93% capacitance retention after 500 cycles at a scan rate of 200mVs(-1)). The obtained results give good prospect about the application of electrostatic coprecipitation method to prepare graphene/metal oxides nanohybrids as effective electrode materials for supercapacitors. Copyright © 2017 Elsevier B.V. All rights reserved.

  12. Rapid Removal of Tetrabromobisphenol A by Ozonation in Water: Oxidation Products, Reaction Pathways and Toxicity Assessment.

    Directory of Open Access Journals (Sweden)

    Ruijuan Qu

    Full Text Available Tetrabromobisphenol A (TBBPA is one of the most widely used brominated flame retardants and has attracted more and more attention. In this work, the parent TBBPA with an initial concentration of 100 mg/L was completely removed after 6 min of ozonation at pH 8.0, and alkaline conditions favored a more rapid removal than acidic and neutral conditions. The presence of typical anions and humic acid did not significantly affect the degradation of TBBPA. The quenching test using isopropanol indicated that direct ozone oxidation played a dominant role during this process. Seventeen reaction intermediates and products were identified using an electrospray time-of-flight mass spectrometer. Notably, the generation of 2,4,6-tribromophenol was first observed in the degradation process of TBBPA. The evolution of reaction products showed that ozonation is an efficient treatment for removal of both TBBPA and intermediates. Sequential transformation of organic bromine to bromide and bromate was confirmed by ion chromatography analysis. Two primary reaction pathways that involve cleavage of central carbon atom and benzene ring cleavage concomitant with debromination were thus proposed and further justified by calculations of frontier electron densities. Furthermore, the total organic carbon data suggested a low mineralization rate, even after the complete removal of TBBPA. Meanwhile, the acute aqueous toxicity of reaction solutions to Photobacterium Phosphoreum and Daphnia magna was rapidly decreased during ozonation. In addition, no obvious difference in the attenuation of TBBPA was found by ozone oxidation using different water matrices, and the effectiveness in natural waters further demonstrates that ozonation can be adopted as a promising technique to treat TBBPA-contaminated waters.

  13. Application of UV and Fluorescence Indices for Assessing the Performance of Ozonation Process: Towards Smart Water Treatment

    Science.gov (United States)

    Li, Wen-Tao; Abbt-Braun, Gudrun; Dodd, Michael; Korshin, Gregory; Li, Ai-Min

    2017-04-01

    The UV absorbance and fluorescence indices were comprehensively studied as surrogate indicators for assessing the degradation of dissolved organic matter (DOM), the formation of bromate and biodegradable dissolved organic carbon (BDOC) and the elimination of trace organic contaminants (TOrCs) during the ozonation of surface water and wastewater effluent. Spectroscopic monitoring was carried out using benchtop UV/Vis and fluorescence spectrophotometers and a newly developed miniature LED UV/fluorescence sensor capable of rapidly measuring UVA280 and protein-like and humic-like fluorescence. With the increase of O3/DOC mass ratio, the plots of BDOC formation were characterized three phases of initial lag, transition slope and final plateau. With the decrease of UV absorbance and fluorescence, BDOC concentrations initially increased slowly and then rose more noticeably. Inflection points in plots of BDOC versus changes of spectroscopic indicators were close to 35-45% loss of UVA254 or UVA280 and 75-85% loss of humic-like fluorescence. According to the data from size exclusion chromatography (SEC) with organic carbon detection and 2D synchronous correlation analyses, DOM fractions assigned to operationally defined large biopolymers (apparent molecular weight, AMW>20 kDa) and medium AMW humic substances (AMW 5.5-20 kDa) were transformed into medium-size building blocks (AMW 3-5.5 kDa) and other smaller AMW species (AMWa similar removal percentage (25-75 %) of TOrCs of group III (e.g. DEET) and IV (e.g. atrazine), and a poor removal percentage (a useful supplement to UVA indices for characterization of ozonation processes.

  14. Titrimetric, spectrophotometric and kinetic methods for the assay of atenolol using bromate–bromide and methyl orange

    Directory of Open Access Journals (Sweden)

    KANAKAPURA BASAVAIAH

    2006-05-01

    Full Text Available Three new methods have been developed for the determination of atenolol in bulk drug and in tablet formulation. The methods are based on the oxidation–bromination reaction of the drug by bromine, generated in situ by the action of acid on a bromate–bromide mixture. In the titrimetric method, the drug is treated with a known excess of bromate–bromide mixture in hydrochloric acid medium, followed by the determination of the unreacted bromine iodometrically. The spectrophotometric method involves the addition of a measured excess of bromate–bromide reagent in hydrochloric acid medium to atenolol, and after ensuring the reaction had gone to completion, the unreacted bromine is treated with a fixed amount of methyl orange, and absorbance measured at 520 nm. The absorbance was found to increase linearly with increasing concentration of atenolol. The kinetic method depends on the existence of a linear relationship between the concentration of the drug and the time of the oxidation–bromination reaction, as indicated by the bleaching of methyl orange acid colour. The working conditions were optimized. The titrimetric method is based on a 1:1 reaction stoichiometry (atenolol:bromate and is applicable over the 3–20 mg range. The spectrophotometric method permits micro determination of the drug (0.5–4.0 mg ml-1with an apparentmolar absorptivity of 4.13x104 lmol-1 cm-1 and detection limit of 0.07 mg ml-1. The kinetic method is applicable in the concentration range 5–25 mg ml-1 with a detection limit of 3.72 mg ml-1. The proposed methods were successfully applied to the determination of atenolol in tablet preparations with mean recoveries of 97.63 to 101.78 %. The reliability of the assay was established by parallel determination by the reference method and by recovery studies using the standard addition technique.

  15. Fabrication, electrochemical and electrocatalytic properties of carbon nanotube@nano-SiO2BenV/phosphomolybdic acid polynary nanocomposite materials

    Science.gov (United States)

    Liu, Jiang; Wang, Jing; Wang, Wen-Bo; Chen, Meng; Qian, Dong-Jin

    2017-06-01

    Organic-inorganic nano-materials have attracted growing attention due to their potential applications for optoelectronic devices, sensors, and heterogeneous catalysts. We reported here on the preparation of polynary nanocomposites composed of poly(4-vinylpyridine) (P4VP) functionalized multi-walled carbon nanotubes (MWNTP4VP), silica nanoparticles (nano-SiO2), viologens, and/or phosphomolybdic acid (PMA), in which the MWNTP4VP, nano-SiO2, and viologens were covalently connected while PMA was electrostatically adsorbed. Thermogravimetric analysis revealed that the nanocomposites were composed of about 40-45% MWNTs, 40-45% nanoSiO2, as well as 10-15% organic species and others. The preparation processes and compositions of the nanocomposites were characterized using Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. Field emission transmission electron microscopic images revealed that the nano-SiO2BenV particles were strongly attached to the MWNTP4VP surfaces to form MWNTP4VP@nano-SiO2BenV triad nano-cores. Cyclic voltammograms of the MWNTP4VP@nano-SiO2BenV casting films showed three couples of redox waves in the potential range between -0.8 and 0 V (vs Ag/AgCl), designated to the electron transfer process of viologen substituents of MWNTP4VP@nano-SiO2BenV2+ ↔ MWNTP4VP@nano-SiO2BenV+rad and their dimers. Further, three couples of redox waves were recorded for the casting films of MWNTP4VP@nano-SiO2BenV/PMA polynary nanocomposites in the potential range between -0.2 and 0.8 V, designated to three successive electron transfer processes of PMA. Finally, it was revealed that the present MWNTPVP@nano-SiO2BenV/PMA polynary composites could act as efficient heterogeneous catalysts for the electrocatalytic reduction of bromate.

  16. Enhanced formation of disinfection byproducts in shale gas wastewater-impacted drinking water supplies.

    Science.gov (United States)

    Parker, Kimberly M; Zeng, Teng; Harkness, Jennifer; Vengosh, Avner; Mitch, William A

    2014-10-07

    The disposal and leaks of hydraulic fracturing wastewater (HFW) to the environment pose human health risks. Since HFW is typically characterized by elevated salinity, concerns have been raised whether the high bromide and iodide in HFW may promote the formation of disinfection byproducts (DBPs) and alter their speciation to more toxic brominated and iodinated analogues. This study evaluated the minimum volume percentage of two Marcellus Shale and one Fayetteville Shale HFWs diluted by fresh water collected from the Ohio and Allegheny Rivers that would generate and/or alter the formation and speciation of DBPs following chlorination, chloramination, and ozonation treatments of the blended solutions. During chlorination, dilutions as low as 0.01% HFW altered the speciation toward formation of brominated and iodinated trihalomethanes (THMs) and brominated haloacetonitriles (HANs), and dilutions as low as 0.03% increased the overall formation of both compound classes. The increase in bromide concentration associated with 0.01-0.03% contribution of Marcellus HFW (a range of 70-200 μg/L for HFW with bromide = 600 mg/L) mimics the increased bromide levels observed in western Pennsylvanian surface waters following the Marcellus Shale gas production boom. Chloramination reduced HAN and regulated THM formation; however, iodinated trihalomethane formation was observed at lower pH. For municipal wastewater-impacted river water, the presence of 0.1% HFW increased the formation of N-nitrosodimethylamine (NDMA) during chloramination, particularly for the high iodide (54 ppm) Fayetteville Shale HFW. Finally, ozonation of 0.01-0.03% HFW-impacted river water resulted in significant increases in bromate formation. The results suggest that total elimination of HFW discharge and/or installation of halide-specific removal techniques in centralized brine treatment facilities may be a better strategy to mitigate impacts on downstream drinking water treatment plants than altering

  17. Mechanism and kinetics of halogenated compound removal by metallic iron: Transport in solution, diffusion and reduction within corrosion films.

    Science.gov (United States)

    Tang, Shun; Wang, Xiao-Mao; Liu, Shi-Ting; Yang, Hong-Wei; Xie, Yuefeng F; Yang, Xiao-Yi

    2017-07-01

    A detailed kinetic model comprised of mass transport (ktra), pore diffusion (kdif), adsorption and reduction reaction (krea), was developed to quantitatively evaluate the effect of corrosion films on the removal rate (kobs) of halogenated compounds by metallic iron. Different corrosion conditions were controlled by adjusting the iron aging time (0 or 1 yr) and dissolved oxygen concentration (0-7.09 mg/L DO). The kobs values for bromate, mono-, di- and tri-chloroacetic acids (BrO3-, MCAA, DCAA and TCAA) were 0.41-7.06, 0-0.16, 0.01-0.53, 0.10-0.73 h-1, with ktra values at 13.32, 12.12, 11.04 and 10.20 h-1, kdif values at 0.42-5.82, 0.36-5.04, 0.30-4.50, 0.30-3.90 h-1, and krea values at 14.94-421.18, 0-0.19, 0.01-1.30, 0.10-3.98 h-1, respectively. The variation of kobs value with reaction conditions depended on the reactant species, while those of ktra, kdif and krea values were irrelevant to the species. The effects of corrosion films on kdif and krea values were responsible for the variation of kobs value for halogenated compounds. For a mass-transfer-limited halogenated compound such as BrO3-, an often-neglected kdif value primarily determined its kobs value when pore diffusion was the rate-limiting step of its removal. In addition, the value of kdif might influence product composition during a consecutive dechlorination, such as for TCAA and DCAA. For a reaction-controlled compound such as MCAA, an increased krea value was achieved under low oxic conditions, which was favorable to improve its kobs value. The proposed model has a potential in predicting the removal rate of halogenated compounds by metallic iron under various conditions. Copyright © 2017. Published by Elsevier Ltd.

  18. The competition between cathodic oxygen and ozone reduction and its role in dictating the reaction mechanisms of an electro-peroxone process.

    Science.gov (United States)

    Xia, Guangsen; Wang, Yujue; Wang, Bin; Huang, Jun; Deng, Shubo; Yu, Gang

    2017-07-01

    Previous studies indicate that effective generation of hydrogen peroxide (H2O2) from cathodic oxygen (O2) reduction is critical for the improved water treatment performance (e.g., enhanced pollutant degradation and reduced bromate formation) during the electro-peroxone (E-peroxone) process (a combined process of electrolysis and ozonation). However, undesired reactions (e.g., O3, H2O2, and H2O reductions) may occur in competition with O2 reduction at the cathode. To get a better understanding of how these side reactions would affect the process, this study investigated the cathodic reaction mechanisms during electrolysis with O2/O3 gas mixture sparging using various electrochemical techniques (e.g., linear sweep voltammetry and stepped-current chronopotentiometry). Results show that when a carbon brush cathode was used during electrolysis with O2/O3 sparging, H2O and H2O2 reductions were usually negligible cathodic reactions. However, O3 can be preferentially reduced at much more positive potentials (ca. 0.9 V vs. SCE) than O2 (ca. -0.1 V vs. SCE) at the carbon cathode. Therefore, cathodic O2 reduction was inhibited when the process was operated under current limited conditions for cathodic O3 reduction. The inhibition of O2 reduction prevented the desired E-peroxone process (cathodic O2 reduction to H2O2 and ensuing reaction of H2O2 with O3 to OH) from occurring. In contrast, when cathodic O3 reduction was limited by O3 mass transfer to the cathode, cathodic O2 reduction to H2O2 could occur, thus enabling the E-peroxone process to enhance pollutant degradation and mineralization. Many process and water parameters (applied current, ozone dose, and reactivity of water constituents with O3) can cause fundamental changes in the cathodic reaction mechanisms, thus profoundly influencing water treatment performance during the E-peroxone process. To exploit the benefits of H2O2 in water treatment, reaction conditions should be carefully controlled to promote cathodic O

  19. Reclaimed water quality during simulated ozone-managed aquifer recharge hybrid

    KAUST Repository

    Yoon, Min

    2014-06-17

    A synergistic hybrid of two treatment processes, managed aquifer recharge (MAR) combined with ozonation, was proposed for wastewater reclamation and water reuse applications. Batch reactor and soil-column experiments were performed to evaluate reclaimed water quality using various chemical and bacterial analyses. The ozone process was optimized at low ozone dose (0.5 mg O3/mg DOC) based on the control of N-nitrosodimethylamine (<5 ng L-1) and bromate (<10 μg L-1), and applied prior to (i.e., O3-MAR) and after MAR (i.e., MAR-O3). This work demonstrates that effluent organic matter (EfOM) and trace organic contaminants (TOrCs) are effectively removed during the hybrid process of MAR combined ozonation, compared to MAR only. Based on fluorescence excitation-emission matrices analyses, both MAR and ozonation reduce soluble microbial (protein-like) products while only ozonation contributes in reducing humic and fulvic substances. Even at low ozone dose of 0.5 mg O3/mg DOC, the O3-MAR hybrid significantly reduced UV absorbance by ≥2 m-1, BDOC by ≥64 %, and total (Σ) TOrC concentrations by ≥70 % in the effluent water quality. However, no significant improvement (<10 %) in the removal of Σ16 TOrC concentrations was observed for the increased ozone dose at 1.0 mg O3/mg DOC during MAR combined ozonation processes. Overall, O3-MAR was effective by 10-30 % in treating effluent water than MAR based on DOC, UV254 nm EfOM, TOrC and bacterial analyses. In addition, MAR-O3 was better than O3-MAR for the reduction of fluorescence (close MQ), TOrCs (≥74 %) and total bacteria cell concentrations (>3 log reduction). Therefore, implementing MAR prior to ozonation appears to remove the bio-amenable compounds that react rapidly with ozone, thereby reducing oxidant demand and treatment efficiency. © 2014 Springer-Verlag Berlin Heidelberg.

  20. An investigation of sodium–CO{sub 2} interaction byproduct cleaning agent for SFR coupled with S-CO{sub 2} Brayton cycle

    Energy Technology Data Exchange (ETDEWEB)

    Jung, Hwa-Young, E-mail: jhy0523@kaist.ac.kr [Department of Nuclear and Quantum Engineering, Korea Advanced Institute of Science and Technology, 373-1 Guseong-dong Yuseong-gu, Daejeon 305-701 (Korea, Republic of); Division of SFR NSSS System Design, Korea Atomic Energy Research Institute, 111, Daedeok-daero 989beon-gil, Yuseong-gu, Daejeon 305-353 (Korea, Republic of); Lee, Jeong Ik, E-mail: jeongiklee@kaist.ac.kr [Department of Nuclear and Quantum Engineering, Korea Advanced Institute of Science and Technology, 373-1 Guseong-dong Yuseong-gu, Daejeon 305-701 (Korea, Republic of); Wi, Myung-Hwan, E-mail: mhwi@kaeri.re.kr [Division of SFR NSSS System Design, Korea Atomic Energy Research Institute, 111, Daedeok-daero 989beon-gil, Yuseong-gu, Daejeon 305-353 (Korea, Republic of); Ahn, Hong Joo, E-mail: ahjoo@kaeri.re.kr [Division of Nuclear Chemistry Research, Korea Atomic Energy Research Institute, 111, Daedeok-daero 989beon-gil, Yuseong-gu, Daejeon 305-353 (Korea, Republic of)

    2016-02-15

    Highlights: • Study on cleaning agent was conducted to remove Na–CO{sub 2} interaction byproducts. • Screening criteria to select candidate substances as cleaning agents were suggested. • The mixtures of Na{sub 2}CO{sub 3} with NaBrO{sub 3}, NaClO{sub 3}, or NaBF{sub 4} were thermally analyzed with the TG/DTA studies. • Three candidate substances decomposed before 600 °C and did not react with Na{sub 2}CO{sub 3}. - Abstract: One of the promising future nuclear energy systems, the Sodium-cooled Fast Reactor (SFR) has been actively developed internationally. Recently, to improve safety and economics of a SFR further, coupling supercritical CO{sub 2} power cycle was suggested. However, there can be a chemical reaction between sodium and CO{sub 2} at high temperature (more than 400 °C) when the pressure boundary fails in a sodium–CO{sub 2} heat exchanger. To ensure the performance of such a system, it is important to employ a cleaning agent to recover the system back to normal condition after the reaction. When sodium and CO{sub 2} react, solid and gaseous reaction products such as sodium carbonate (Na{sub 2}CO{sub 3}) and carbon monoxide (CO) appear. Since most of solid reaction products are hard and can deteriorate system performance, quick removal of solid reaction products becomes very important for economic performance of the system. Thus, the authors propose the conceptual method to remove the byproducts with a chemical reaction at high temperature. The chemical reaction will take place between the reaction byproducts and a cleaning agent while the cleaning agent is inert with sodium. Thus, various sodium-based compounds were first investigated and three candidate substances satisfying several criteria were selected; sodium bromate (NaBrO{sub 3}), sodium chlorate (NaClO{sub 3}), and sodium tetrafluoroborate (NaBF{sub 4}). The selected substances were thermally analyzed with the TG/DTA studies. Unfortunately, it was revealed that all candidate

  1. Porous Si layers-Preparation, characterization and morphology

    Energy Technology Data Exchange (ETDEWEB)

    Badawy, Waheed A., E-mail: wbadawy@cu.edu.e [Chemistry Department, Faculty of Science, Cairo University, Gamaa Street, 12 613 Giza (Egypt); El-Sherif, Rabab M.; Khalil, Shaaban A. [Chemistry Department, Faculty of Science, Cairo University, Gamaa Street, 12 613 Giza (Egypt)

    2010-12-01

    Porous silicon layers (PSL) of nano- and micro-structures were prepared by metal-assisted electroless etching of silicon in HF-oxidizing agent aqueous solutions. The effect of oxidizing agent and HF content on the characteristics of the formed porous layers was investigated. A thin Pt film was electroless deposited on p-Si<1 0 0> prior to immersion in the etching solution. The properties and morphology of the PSL formed by this method were investigated by electrochemical impedance spectroscopy (EIS) scanning electron microscopy (SEM) and energy dispersive X-ray (EDX) technique. The characteristics of the PSL were found to be affected by the constituents of the etching medium and also, the etching time. Potassium bromate (KBrO{sub 3}), potassium iodate (KIO{sub 3}), and potassium dichromate (K{sub 2}Cr{sub 2}O{sub 7}) have been used as oxidizing agents. Pt-assisted etching of p-Si for 1 h in an etching solution consisting of 22.0 M HF and 0.05 M of KBrO{sub 3}, results in the formation of nano- and micro-pores on the Si surface. The use of 0.05 M KIO{sub 3} or K{sub 2}Cr{sub 2}O{sub 7} as oxidizing agent has led to the formation of a deposit on the silicon surface. At relatively higher concentration [>0.05 M] of K{sub 2}Cr{sub 2}O{sub 7} the surface deposit becomes clear and was found to consist of an insoluble passive solid-phase of K{sub 2}SiF{sub 6} which increases the film impedance and blocks the porous structure formation. The use of higher concentration [>22 M] of HF in the etching electrolyte is accompanied by an increase in the dissolution rate of the insoluble K{sub 2}SiF{sub 6} layer and a decrease in the PSL passivity. The experimental impedance data were fitted to theoretical data according to a proposed equivalent circuit model which accounts for the mechanism of the porous film formation at the Si/electrolyte interface.

  2. Mapeamento da qualidade da água de abastecimento público no nordeste do estado de São Paulo (Brasil | Mapping of public water supply in the northeast of the State of São Paulo (Brazil

    Directory of Open Access Journals (Sweden)

    Sergio Dovidauskas

    2017-05-01

    nitrate concentration was greater than the maximum value allowed in 17 samples; 1730 samples showed fluoride content out-of-range of drinking pattern; bromate concentration was greater than the maximum value allowed in 16 samples; the pH value was outside the range recommended in 161 samples; 292 samples showed levels of free residual chlorine (FRC outside the recommended range; 17 samples showed apparent color values above the maximum allowed; 13 samples showed turbidity values above the maximum allowed. By means of principal components analysis, it was possible to discriminate the waters of the region, with the formation of groups of municipalities with similar physico-chemical profiles, generating a mapping based on prominent variables.

  3. Recent advances in drinking water disinfection: successes and challenges.

    Science.gov (United States)

    Ngwenya, Nonhlanhla; Ncube, Esper J; Parsons, James

    2013-01-01

    Drinking water is the most important single source of human exposure to gastroenteric diseases, mainly as a result of the ingestion of microbial contaminated water. Waterborne microbial agents that pose a health risk to humans include enteropathogenic bacteria, viruses, and protozoa. Therefore, properly assessing whether these hazardous agents enter drinking water supplies, and if they do, whether they are disinfected adequately, are undoubtedly aspects critical to protecting public health. As new pathogens emerge, monitoring for relevant indicator microorganisms (e.g., process microbial indicators, fecal indicators, and index and model organisms) is crucial to ensuring drinking water safety. Another crucially important step to maintaining public health is implementing Water Safety Plans (WSPs), as is recommended by the current WHO Guidelines for Drinking Water Quality. Good WSPs include creating health-based targets that aim to reduce microbial risks and adverse health effects to which a population is exposed through drinking water. The use of disinfectants to inactivate microbial pathogens in drinking water has played a central role in reducing the incidence of waterborne diseases and is considered to be among the most successful interventions for preserving and promoting public health. Chlorine-based disinfectants are the most commonly used disinfectants and are cheap and easy to use. Free chlorine is an effective disinfectant for bacteria and viruses; however, it is not always effective against C. parvum and G. lamblia. Another limitation of using chlorination is that it produces disinfection by-products (DBPs), which pose potential health risks of their own. Currently, most drinking water regulations aggressively address DBP problems in public water distribution systems. The DBPs of most concern include the trihalomethanes (THMs), the haloacetic acids (HAAs), bromate, and chlorite. However, in the latest edition of the WHO Guidelines for Drinking Water Quality

  4. Cinética ruminal da fração fibrosa de volumosos para ruminantes Ruminal kinetics of the fibrous fraction of ruminant roughages

    Directory of Open Access Journals (Sweden)

    Elaine Barbosa Muniz

    2012-09-01

    Full Text Available Os objetivos do presente trabalho foram a caracterização e a determinação das estimativas dos parâmetros relativos à cinética de degradação ruminal da fibra em detergente neutro (FDN dos fenos de mata pasto, juazeiro, mororó, aveia e Tifton 85 e silagens de milho, sorgo e palma forrageira. Foram determinados a composição químico-bromatólogica, os coeficientes de degradação e o efeito de repleção ruminal da FDN. As características químico-bromatológicas dos alimentos avaliados apresentaram variações em seus componentes nutricionais. A fração insolúvel potencialmente degradável da FDN, correspondente à fração B2 dos alimentos estudados, apresentou degradação variável. Os fenos de mata pasto, juazeiro e mororó apresentaram menores valores para a fração potencialmente degradável. As silagens de milho e sorgo apresentaram uma pequena variação para a fração potencialmente degradável e para a fração indigestível, assim como, para a taxa de degradação da FDN potencialmente digestível. O maior tempo de retenção total foi observado para mata pasto, juazeiro e mororó, seguidos pelas silagens, sendo constatados para os fenos de aveia e Tifton 85 os menores valores para esta variável. As forrageiras de regiões semiáridas avaliadas (mata pasto, juazeiro e mororó podem limitar o consumo de matéria seca devido aos menores valores da fração potencialmente degradável e maiores valores da fração indigestível. O efeito de repleção ruminal da FDN é determinado pela integração de várias características da fibra. Dessa maneira, não se pode atribuir a toda e qualquer fonte de fibra as mesmas inferências restritivas à limitação física de consumo.The objectives of the present work were to characterize and determine the estimates of the parameters relating to the kinetics of ruminal degradation of neutral detergent fiber (NDF in hays from forest pasture, the jujube plant, mororo, oats and Tifton 85