WorldWideScience

Sample records for bromates

  1. 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 Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN... Specific Usage Additives § 172.730 Potassium bromate. The food additive potassium bromate may be...

  2. 21 CFR 137.205 - Bromated whole wheat flour.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 2 2010-04-01 2010-04-01 false Bromated whole wheat flour. 137.205 Section 137... Cereal Flours and Related Products § 137.205 Bromated whole wheat flour. Bromated whole wheat flour... of ingredients, prescribed for whole wheat flour by § 137.200, except that potassium bromate is...

  3. 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.

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

    Science.gov (United States)

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

    2015-04-01

    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 necessary and other drugs with potential ototoxicity should be avoided. The outcome of cochlear implantation was excellent in this case of bromate-induced deafness.

  5. 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...... reduced by each pretreatment while the required ozone dose for 90% atrazine removal increased at different degree for each pre-treatment....

  6. 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)...

  7. A new electrochemical oscillatory system of bromate in alkaline solution

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    A new electrochemical oscillatory system of bromate in alkaline solution is reported. In PtBromate-Alkaline solution system, two different types of electrochemical oscillations (Type Ⅰ and Type Ⅱ) can be observed. Type Ⅰ appears before hydrogen evolution and Type Ⅱ involves periodic hydrogen evolution. Type Ⅰ relates to the adsorption/desorption of the hydrogen on platinum electrode, and Type Ⅱ with periodic oscillation stems from the coupling of electrochemical reactions (the reduction of bromate and evolution hydrogen reaction) with mass transfer (diffusion and convection). More over, under the right conditions, the two types appear in different oscillatory modes, for example,simple periodical mode and mixed one, etc,, Crossed cycle in the cyclic voltammograms, which is the basiccharacteristics for electrochemical oscillatory systems, has also been observed as expected.

  8. 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.

  9. 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.

  10. 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...

  11. Control of Bromate and THM Precursors Using Ozonation Combined System

    Institute of Scientific and Technical Information of China (English)

    SHU-GUANG XIE; DONG-WEN SHI; DONG-HUI WEN; RUI WANG; DAN-LI XI

    2007-01-01

    Objective To investigate the feasibility of reducing THM precursors and controlling bromate taste and odor in drinking water taken from the Yellow River by an ozonation combined system. Methods The appropriate ozone dosage was determined,and then the changes of TOC,UV254 and THM formation potential(THMFP)in the combined system were evaluated. Results One mg/L ozone could effectively remove taste and odor and meet the maximum allowable bromate level in drinking water.The pre-ozonation increased THMFP,but the conventional treatment system could effectively reduce the odor.The bio-ceramic filter could partly reduce CHCI3FP,but sometimes might increase CHCI2BrFP and CHCIBr2FP.The biological activated carbon(BAC)filter could effectively reduce CHCI3FP and CHCI2BrFP,but increase CHCIBr2FP.Compared with other filters.the fresh activated carbon(FAC)filter performed better in reducing THMFP and even reduced CHCIBrzFP.Conclusion The combined system can effectively reduce taste,odor,CHCI3FP,and CHCI2BrFP and also bring bromate under control.

  12. 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...

  13. Bromate ion formation in dark chlorination and ultraviolet/chlorination processes for bromide-containing water

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Bormate (BrO3-) is a carcinogenic chemical produced in ozonation or chlorination of bromide-containing water. Although its formation in seawater with or without sunlight has been previously investigated, the formation of bromate in dilute solutions,particularly raw water for water treatment plant, is unknown. In this article, the results of bench scale tests to measure the formation rates of bromate formation in dilute solutions, including de-ionized water and raw water from Yangtze River, were presented in dark chlorination and ultraviolet (UV)/chlorination processes. And the effects of initial pH, initial concentration of NaOCl, and UV light intensity on bromate formation in UV/chlorination of the diluted solutions were investigated. Detectable bromate was formed in dark chlorination of the two water samples with a relatively slow production rate. Under routine disinfecting conditions, the amount of formed bromate is not likely to exceed the national standards (10 μg/L). UV irradiation enhanced the decay of free chlorine, and,simultaneously, 6.6%-32% of Br- was oxidized to BrO3-. And the formation of bromate exhibited three stages: rapid stage, slow stage and plateau. Under the experimental conditions (pH = 4.41-11.07, CCl2= 1.23-4.50 mg/L), low pH and high chlorine concentration favored the generation of bromate. High light intensity promoted the production rate of bromate, but decreased its total generation amount due to acceleration of chlorine decomposition.

  14. Stirring and mixing effects on oscillations and inhomogeneities in the minimal bromate oscillator

    Science.gov (United States)

    Dutt, A. K.; Menzinger, M.

    1999-04-01

    Stirring and mixing effects on the oscillations and inhomogeneities in the bromate-bromide-cerous system (minimal bromate oscillator) have been investigated in a continuously fed stirred tank reactor (CSTR). A movable microelectrode is used to monitor the inhomogeneities inside the CSTR in an oscillating phase. The results are explained in terms of the theory of imperfect mixing.

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

    Institute of Scientific and Technical Information of China (English)

    Ji Li; Li Zou; Lulu Guo; Jialin Ji

    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 0.20mg/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.

  16. Effects of ion-exchange treatment on bromate formation and oxidation efficiency during ozonation

    OpenAIRE

    Echigo, S.; Itoh, S.; Niwa, A

    2012-01-01

    Ion-exchange treatment is a promising technique for removing hydrophilic compounds during drinking water treatment. In this study, we applied several different ion exchangers (i.e., anion exchange resins and a hydrotalcite compound) to bromide removal to minimize bromate formation during ozonation. It was found that ion-exchange treatment affected ozone and hydroxyl radical concentration profiles as well as bromate ion concentration after ozonation. Selecting an appropriate ion exchanger is i...

  17. Bistability in an uncatalyzed bromate oscillator in a continuously fed stirred tank reactor

    Science.gov (United States)

    Dutt, Arun K.; Müller, S. C.

    1996-01-01

    Uncatalyzed gallic acid oscillating system has been investigated in a continuously fed stirred tank reactor (CSTR). In the [Bromate]0-[Bromide]0 concentration space, a region has been located where a bistability is observed between an oscillatory branch and a flow branch. To our knowledge this is the first evidence of bistability in an uncatalyzed bromate oscillator. Some observations have been explained in terms of the skeleton mechanism proposed in the past.

  18. [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.

  19. 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.

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

    Directory of Open Access Journals (Sweden)

    Alanowd O. Mehder

    2015-06-01

    Full Text Available 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 samples of food stuffs.

  1. Bromate formation on the non-porous TiO2 photoanode in the photoelectrocatalytic system.

    Science.gov (United States)

    Selcuk, Huseyin; Sarikaya, Hasan Z; Bekbolet, Miray; Anderson, Marc A

    2006-02-01

    The increasing use of ozone in water disinfection processes has been the focus of considerable concern in regards to inorganic disinfection by product formation of bromate in waters containing bromide. Due to the public health risk caused by the presence of bromate as a suspected carcinogen, attention had been addressed to the conditions under which bromate is formed. In this study, photoanodic bromine generation and bromate (BrO(3)(-)) formation were investigated using a TiO(2) electrode in a photoelectrocatalytic (PEC) treatment process. The separation of anodic and cathodic reactions in the PEC system resulted in a pH decrease from 9.3 to 3.0 in the photoanode compartment and an increase to 11.0 in the cathode compartment. Under a photo-illumination intensity of 5.7 m W cm(-2) UV, a biasing potential of +1.0V vs SCE, a pH of 6.0 and at a NaBr concentration of 1.0 x 10(-2) M, active bromine formation increased over time with 2.4 x 10(-6) M min(-6) rate and reached a steady-state concentration of 1.44 x 10(-4) M in 60 min. Bromate formation was detected after a lag-period of 15 min and exhibited a continuous increasing trend with respect to irradiation time. No bromate formation was observed below pH 6.5 whereas an increasing bromate concentrations and pH up to pH=8.5 were noted.

  2. 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.

  3. [Peripheral nerve disease associated with acute renal failure due to bromate poisoning].

    Science.gov (United States)

    Deshimaru, M; Miyagawa, T; Sumiyoshi, S; Nomura, Y

    1976-08-01

    A case of 21 year old male with neuropathy caused by renal insufficiency was present. He had taken bromate (mixed powder of potassium bromate and sodium bromate) for the purpose of suicide and suffered from acute renal insufficiency and hard of hearing. Renal dysfunction improved gradually by peritoneal dialysis and hemodialysis. However, on the 32th day after the onset, burning pain appeared in the bilateral feets. Following this, he began to complain of the disturbances of superficial and deep sensory below the ankle jerks and the weakness of his toes. Considering the clinical features, we supposed that the disturbance of the peripheral nerve was caused by uremia due to taking bromate. N. suralis was biopsied on the 80th day after the onset and examined electron microscopically. Electroscopical findings was as follows. Degeneration of the Schwann cells and irregularity or destruction of the myelin sheaths were observed. The axoplasm of the myelinated nerve fiber were relatively preserved as compared with the changes of the myelin sheaths. In the unmyelinated nerve fibers, cavity formations were observed. The findings of regeneration were not observed. From the electron microscopical findings, we speculate that the changes of the Schwann cells and the myelin sheaths are primary resulting from the disturbance of the metabolism of the Schwann cells. We speculate that anemia and hypoproteinemia caused by bromate disturbed regeneration.

  4. 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...... is of high interest. This study tested improvements to conventional ozonation that reduce the formation of the oxidation-by-product bromate, while maintaining the effectiveness for removal emerging contaminants (atrazine). MnO4−, ClO2−, ClO2, ClO−, CH3COOO−, HSO5− or S2O8−2 with NH4+ were tested as pre......-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...

  5. 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.

  6. Selenium dioxide catalysed oxidation of acetic acid hydrazide by bromate in aqueous hydrochloric acid medium

    Indian Academy of Sciences (India)

    R S Yalgudre; G S Gokavi

    2012-07-01

    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. The mechanism of the reaction involves prior complex formation between the catalyst and substrate, hydrazide, followed by its oxidation by diprotonated bromate in a slow step. Acetic acid was found to be the oxidation product. Other kinetic data like effect of solvent polarity and ionic strength on the reaction support the proposed mechanism.

  7. 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.

  8. 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. ...

  9. 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...

  10. 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.

  11. 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.

  12. Valorization of aluminum scrap via an acid-washing treatment for reductive removal of toxic bromate from water.

    Science.gov (United States)

    Lin, Kun-Yi Andrew; Lin, Jia-Yin; Lien, Hsing-Lung

    2017-04-01

    Aluminum scrap (AS) is adopted for the first time as a readily available aluminum source to prepare zero-valent aluminum (ZVAl) for removing bromate from water via a reductive reaction. Since aluminum is easily oxidized to aluminum oxide (Al2O3) on exposure to air, an acid-washing pretreatment on AS is developed to remove the layer of Al2O3. HCl is found as the most effective acid to pretreat AS and the HCl-pretreated or acid-washed AS (AWAS) is able to remove bromate from water and convert it to bromide. Factors, such as temperature, pH, co-existing anions, and particle size, which influence the bromate removal using AWAS are also investigated. The mechanism of bromate removal by AWAS can be attributed to both reduction and adsorption. The elevated temperature also significantly improves bromate removal capacity of AWAS as well as the reaction kinetics. The bromate removal capacity of AWAS is substantially improved under acidic conditions. However, the basic conditions and co-existing anions suppress or interfere with the interaction between bromate and AWAS, leading to much lower removal capacities. The recyclability of AWAS is also evaluated and the acid-washing regeneration is necessary to restore its capacity. However, the mass of AWAS can gradually decrease due to multi-cycle acid-washing regeneration. Through this study, the valorization of AS via acid-washing is demonstrated and optimization of acid-washing parameters is presented. Our findings reveal that the acid-washing is a useful technique to utilize AS as an inexpensive and efficient material for removing bromate from water.

  13. Research strategy for developing key information on bromate's mode of action.

    Science.gov (United States)

    Bull, Richard J; Cottruvo, Joseph A

    2006-04-17

    Bromate is produced when ozone is used to treat waters that contain trace amounts of bromide ion. It is also a contaminant of hypochlorite solutions produced by electrolysis of salt that contains bromide. Both ozone and hypochlorite are extensively used to disinfect drinking water, a process that is credited with reducing the incidence of waterborne infections diseases around the world. In studies on experimental animals, bromate has been consistently demonstrated to induce cancer, although there is evidence of substantial species differences in sensitivity (rat>mouse>hamster). There are no data to indicate bromate is carcinogenic in humans. An issue that is critical to the continued use of ozone as a disinfectant for drinking water in bromide-containing waters depends heavily on whether current predictions of carcinogenic risk based on carcinogenic responses in male rats treated with bromate are accurate at the much lower exposure levels of humans. Thiol-dependent oxidative damage to guanine in DNA is a plausible mode of action for bromate-induced cancer. However, other mechanisms may contribute to the response, including the accumulation of alpha2u-globulin in the kidney of the male rat. To provide direction to institutions that have an interest in clarifying the toxicological risks that bromate in drinking water might pose, a workshop funded by the Awwa Research Foundation was convened to lay out a research strategy that, if implemented, could clarify this important public health issue. The technical issues that underlie the deliberations of the workshop are provided in a series of technical papers. The present manuscript summarizes the conclusions of the workgroup with respect to the type and timing of research that should be conducted. The research approach is outlined in four distinct phases that lay out alternative directions as the research plan is implemented. Phase I is designed to quantify pre-systemic degradation, absorption, distribution, and

  14. Oscillatory bromate-oxalic acid-Ce-acetone-sulfuric acid reaction, in CSTR

    OpenAIRE

    Pereira,Janaina A. M.; Roberto B Faria

    2004-01-01

    Periodic oscillations were observed for the first time, in a CSTR, in the system bromate-oxalic acid-Ce(IV)-acetone-sulfuric acid, in a CSTR. A reaction between Ce(IV) and acetone, until now not described in the literature and occurring before the addition of the reagents to the reactor, was identified as a decisive factor for the appearing of the regular oscillations.

  15. Electrochemical fabrication of copper-containing metal-organic framework films as amperometric detectors for bromate determination.

    Science.gov (United States)

    Shi, Erbin; Zou, Xiaoqin; Liu, Jia; Lin, Huiming; Zhang, Feng; Shi, Shaoxuan; Liu, Fenghua; Zhu, Guangshan; Qu, Fengyu

    2016-05-04

    A facile electrochemical plating strategy has been employed to prepare the electroactive metal-organic framework film (NENU-3) onto a copper electrode in the acid electrolyte containing 1,3,5-benzenetricarboxylic acid (H3BTC) and phosphotungstic acid (PTA). The as-made NENU-3 films have been characterized using powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), Fourier transform infrared (FT-IR) spectroscopy and thermogravimetric analyses (TGA). These analyses indicate that NENU-3 films have high phase purity and high stability. Further, different electrochemical techniques are utilized for measuring the electrochemical behaviors of the NENU-3 film electrodes. Accordingly, the kinetic parameters of a NENU-3 film electrode towards the electrocatalytic reduction of bromate are obtained, including the electron transfer coefficient (α), the catalytic rate constant (ks), and the diffusion coefficient (D). The film electrodes present excellent electrocatalytic ability for the bromate reduction, and can be used successfully for the amperometric detection of bromate. Under the optimized conditions, the proposed sensor exhibits a wide linear range (0.05-72.74 mM) and a lower detection limit (12 μM) measured by chronoamperometry (CA). Moreover, the films possess high electrochemical stability and strong anti-interference capability in the bromate detection process. It has been demonstrated that the electrochemical plating method reported here offers a reliable and efficient way to fabricate MOF films on conductive substrates for bromate detection.

  16. 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.

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

    Indian Academy of Sciences (India)

    K Kishan Rao; V Surender

    2001-12-01

    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 systematically oriented growth hillocks are observed almost on all the faces. Further dislocation studies are made to understand the growth history of these crystals. These studies suggest that the crystals grow by 2D-growth mechanism. In addition to this, studies are also conducted on the formation of overgrowths and inclusions in these crystals.

  18. 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.

  19. Complex dynamic behavior in the bromate-oxalic acid-acetone-Mn(II) oscillating reaction in a continuous stirred tank reactor (CSTR)

    Science.gov (United States)

    Silva, Lucyane C.; Faria, Roberto B.

    2007-05-01

    The oscillating reaction bromate-oxalic acid-acetone-Mn(II)-sulfuric acid was observed for the first time in a CSTR at 20 °C. Depending on the bromate concentrations and flow rate, the system showed large amplitude oscillations, two kinds of mixed mode oscillations, quasiperiodicity and bursts of large amplitude oscillations, all mapped in a phase diagram. More complex behavior was favored at low bromate concentrations. The system without acetone was discovered to oscillate too, but the more complex patterns were not seen, indicating that acetone is implied in their formation.

  20. 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...

  1. 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.

  2. Determination of bromate in drinking water by zone electrophoresis-isotachophoresis on a column-coupling chip with conductivity detection.

    Science.gov (United States)

    Bodor, Róbert; Kaniansky, Dusan; Masár, Marián; Silleová, Katarína; Stanislawski, Bernd

    2002-10-01

    The use of capillary zone electrophoresis (CZE) on-line coupled with isotachophoresis (ITP) sample pretreatment (ITP-CZE) on a poly(methylmethacrylate) chip, provided with two separation channels in the column-coupling (CC) arrangement and on-column conductivity detection sensors, to the determination of bromate in drinking water was investigated. Hydrodynamic and electroosmotic flows of the solution in the separation compartment of the chip were suppressed and electrophoresis was a dominant transport process in the ITP-CZE separations. A high sample load capacity, linked with the use of ITP in this combination, made possible loading of the samples by a 9.2 microL sample injection channel of the chip. In addition, bromate was concentrated by a factor of 10(3) or more in the ITP stage of the separation and, therefore, its transfer to the CZE stage characterized negligible injection dispersion. This, along with a favorable electric conductivity of the carrier electrolyte solution, contributed to a 20 nmol/L (2.5 ppb) limit of detection for bromate in the CZE stage. Sample cleanup, integrated into the ITP stage, effectively complemented such a detection sensitivity and bromate could be quantified in drinking water matrices when its concentration was 80 nmol/L (10 ppb) or slightly less while the concentrations of anionic macroconstituent (chloride, sulfate, nitrate) in the loaded sample corresponding to a 2 mmol/L (70 ppm) concentration of chloride were still tolerable. The samples containing macroconstituents at higher concentrations required appropriate dilutions and, consequently, bromate in these samples could be directly determined only at proportionally higher concentrations.

  3. 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.

  4. EFFECTS OF POTASSIUM BROMATE ON THE KIDNEY AND HAEMATOLOGICAL PARAMETERS OF SWISS ALBINO MICE

    Directory of Open Access Journals (Sweden)

    MARIA STUTI

    2013-01-01

    Full Text Available The present study aimed to investigate the possible effects of potassium bromate toxicity on histological,haematological and biochemical parameters in Swiss albino mice. Mice were orally administered with potassiumbromate at the rate of 150 mg/kg body weight daily in a single dose for 30, 60 and 120 days. The chemicalsignificantly reduced the RBC count (p<0.01 Hb% (p<0.01 and platelet count (p<0.01, while it increasedsignificantly the urea (p<0.01 and creatinine level (p<0.01 and decreased total protein and Albumin (p<0.01Histopathological examination showed degenerative changes of tubular cells, cytoplasma vacuolation, cellularinfiltration, tubular dilation with eosinophilic debris and clear cell cytoplasm were observed. These findingssuggest that KBrO3 affects the physiological and biochemical activities of Swiss albino mice

  5. Effect of temperature in cerium-ion-catalyzed bromate-driven oscillators

    Science.gov (United States)

    Nagy, Gabriella; Körös, Endre; Oftedal, Norunn; Tjelflaat, Kjetil; Ruoff, Peter

    1996-03-01

    The influence of substrate composition and initial reagent concentrations on activation energies in closed Ce-ion catalyzed Belousov-Zhabotinsky (BZ) reactions is reported. While changes in the initial concentration of organic substrate, bromate ion or sulfuric acid showed different changes in activation energies for the various organic substrate BZ systems, for all systems it was found that lowering the Ce-ion concentration leads to a significant decrease in the overall activation energy of the oscillator. When comparing the performance of a malonic acid oscillator run in a batch or in a continuous stirred flow reactor (CSTR), it was found that under CSTR conditions Q10 values may become as low as 1.3, while for the batch system the corresponding Q10 values are about 2.3.

  6. Electrocatalytic reduction of bromate based on Pd nanoparticles uniformly anchored on polyaniline/SBA-15.

    Science.gov (United States)

    Sun, Chencheng; Deng, Ning; An, Hao; Cui, Hao; Zhai, Jianping

    2015-12-01

    A nano-composite electrocatalyst of Pd nanoparticles (Pd-NPs) anchored on polyaniline (PANI) supported by mesoporous SBA-15 (Pd-NPs/PANI/SBA-15), was synthesized using an in situ chemical method. Transmission electron microscopy showed that the Pd-NPs were homogeneously dispersed. Fourier-transform infrared and X-ray photoelectron spectroscopies confirmed that the Pd-NPs in the metallic state (Pd(0)) were predominantly immobilized on nitrogen sites in the PANI chains. The electrochemical performance of Pd-NPs/PANI/SBA-15 for electrocatalytic reduction of bromate (BrO3(-)) in an acidic medium was investigated by cyclic voltammetry (CV) and amperometric measurement. The reduction peak in the CV curves in the region 0.12 to -0.22V (vs. SCE) corresponded to response of BrO3(-) electroreduction, and the reduction peak current was well fitted linearly to the BrO3(-) concentration. It is proposed that the bromate ions diffuse to the Pd-NPs active sites and then the electrocatalytic reduction occurred with the H(+) doped in PANI. Furthermore, by amperometric measurement, Pd-NPs/PANI/SBA-15 showed relatively high sensitivity with respect to BrO3(-) concentration in the range of 8μmolL(-1) to 40mmolL(-1). Continuous CV for 200 cycles proved that Pd-NPs/PANI/SBA-15 had excellent electrocatalytic stability. These results show that Pd-NPs/PANI/SBA-15 is effective for electrocatalytic reduction of BrO3(-) and has great potential for the fabrication of BrO3(-) electrochemical sensor.

  7. 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.

  8. 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

  9. 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

  10. [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.

  11. 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).

  12. 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.

  13. 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.

  14. 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.

  15. 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.

  16. 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.

  17. 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}.

  18. 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)

  19. 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.

  20. 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.

  1. Spectrophotometric Method for Estimation of Tamsulosin Hydrochloride in Pharmaceutical Dosage Form Using Bromate-Bromide and Methyl Orange Reagent

    Directory of Open Access Journals (Sweden)

    Bharatkumar Ganeshbhai Chaudhari

    2012-09-01

    Full Text Available A simple, rapid, accurate and precise assay procedure based on Spectrophotometric method has been developed for the estimation of Tamsulosin hydrochloride in Pharmaceutical formulation. The method was based on the bromination of Tamsulosin hydrochloride with a known excess amount of Bromate-bromide mixture in acidic medium followed by the determination of surplus bromine by reacting with dye methyl orange and measuring the absorbance at 513 nm. Validation was carried out in compliance with International Conference on Harmonization guidelines. Linear regression analysis of method showed good linearity with the correlation co-efficient (r of 0.9978 with respect to absorbance in the concentration range of 2-12 μg/mL and the mean recovery for Tamsulosin hydrochloride was 99.65% ± 0.47 . The proposed method can be successfully applied for the analysis of tablet formulations.

  2. 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.

  3. On-line capillary isotachophoresis-capillary zone electrophoresis analysis of bromate in drinking waters in an automated analyzer with coupled columns and photometric detection.

    Science.gov (United States)

    Marák, Jozef; Staňová, Andrea; Vaváková, Veronika; Hrenáková, Martina; Kaniansky, Dušan

    2012-12-07

    A new, sensitive, and robust analytical method based on capillary zone electrophoresis with on-line capillary isotachophoresis sample pretreatment (ITP-CZE) using a column-coupling (CC) arrangement of automated capillary electrophoretic analyzer was developed for determination of bromate in different type of drinking water samples. Both columns were provided with contact-less conductivity detectors and in CZE step UV detection at 200 nm wavelength was used. Electroosmotic flow of the buffer solutions was suppressed with the addition of 0.1% or 0.05% (m/v) methylhydroxyethylcellulose into the leading and terminating electrolyte, respectively. Hydrodynamic and electroosmotic flows of the buffer solutions were successfully suppressed and therefore, only the electrophoretic transport of ions was significant. Limit of detection for bromate approaching 0.6 μg/L was achieved. Good repeatabilities of migration time (RSD less than 0.3%) and peak area (RSD less than 4.0%) at concentration level 1 μg/L were obtained. Robustness of proposed ITP-CZE method and validation parameters were evaluated. Developed automated ITP-CZE method was applied to the determination of bromate in drinking water samples with different content of inorganic macroconstituents without the need of further sample preparation.

  4. 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.

  5. 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.

  6. 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.

  7. Tephrosia purpurea ameliorates N-diethylnitrosamine and potassium bromate-mediated renal oxidative stress and toxicity in Wistar rats.

    Science.gov (United States)

    Khan, N; Sharma, S; Alam, A; Saleem, M; Sultana, S

    2001-06-01

    In an earlier communication, we have shown that Tephrosia purpurea ameliorates benzoyl peroxide-induced oxidative stress in murine skin (Saleem et al. 1999). The present study was designed to investigate a chemopreventive efficacy of T purpurea against N-diethylnitrosamine-initiated and potassium bromate-mediated oxidative stress and toxicity in rat kidney. A single intraperitoneal dose of N-diethylnitrosamine (200 mg/kg body weight) one hr prior to the dose of KBrO3 (125 mg/kg body weight) increases microsomal lipid peroxidation and the activity of xanthine oxidase and decreases the activities of renal antioxidant enzymes viz., catalase, glutathione peroxidase, glutathione reductase and glucose-6-phosphate dehydrogenase, phase II metabolizing enzymes such as glutathione-S-transferase and quinone reductase and causes depletion in the level of renal glutathione content. A sharp increase in blood urea nitrogen and serum creatinine has also been observed. Prophylactic treatment of rats with T. purpurea at doses of 5 mg/kg body weight and 10 mg/kg body weight prevented N-diethylnitrosamine-initiated and KBrO3 promoted renal oxidative stress and toxicity. The susceptibility of renal microsomal membrane for iron ascorbate-induced lipid peroxidation and xanthine oxidase activities were significantly reduced (Ppurpurea besides a skin antioxidant can be a potent chemopreventive agent against renal oxidative stress and carcinogenesis induced by N-diethylnitrosamine and KBrO3.

  8. Kinetics and mechanism of oxidation of dimethyl sulphoxide by sodium bromate-sodium bisulphite reagent in aqueous medium

    Indian Academy of Sciences (India)

    J Viroopakshappa; V Jagannadham

    2002-04-01

    Rates of oxidation of dimethyl sulphoxide (DMSO) by HOBr produced in situ from sodium bromate-sodium bisulphite reagent have been studied iodometrically in aqueous medium. The order in [DMSO] is one when [DMSO] < 0.01 mol dm-3, fractional when [DMSO] is between 0.01 and 0.5 mol dm-3 and zero when (DMSO) < 0.5 mol dm-3. Different rate laws are operative under these three conditions though HOBr is the effective oxidizing species in all the cases. A mechanism involving an intermediate four-membered cyclic transition state between DMSO and HOBr (formation constant ), which decomposes in a slow step with a rate constant () has been proposed. Thermodynamic parameters for the adduct formation step and activation parameters for the first-order decomposition of the adduct step have been evaluated in the temperature range 308-323 K. Activation parameters have also been determined while the orders in [DMSO] are unity and zero. The reaction product has been identified as dimethyl sulphone (DMSO2).

  9. Formation potentials of bromate and brominated disinfection by-products in bromide-containing water by ozonation.

    Science.gov (United States)

    Lin, Tao; Wu, Shouke; Chen, Wei

    2014-12-01

    The ozonation involved in drinking water treatment raises issues of water quality security when the raw water contains bromide (Br(-)). Br(-) ions may be converted to bromate (BrO3 (-)) during ozonation and some brominated disinfection by-products (Br-DBPs) in the following chlorination. In this study, the effects of ozone (O3) dosage, contact time, pH, and Br(-) and ammonia (NH3-N) concentrations on the formation of BrO3 (-) and Br-DBPs have been investigated. The results show that decreasing the initial Br(-) concentration is an effective means of controlling the formation of BrO3 (-). When the concentration of Br(-) was lower than 100 μg/L, by keeping the ratio of O3 dosage to dissolved organic carbon (DOC) concentration at less than 1, BrO3 (-) production was effectively suppressed. The concentration of BrO3 (-) steadily increased with increasing O3 dosage at high Br(-) concentration (>900 μg/L). Additionally, a longer ozonation time increased the concentrations of BrO3 (-) and total organic bromine (TOBr), while it had less impact on the formation potentials of brominated trihalomethanes (Br-THMFP) and haloacetic acids (Br-HAAFP). Higher pH value and the presence of ammonia may lead to an increase in the formation potential of BrO3 (-) and Br-DBPs.

  10. 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.

  11. 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

  12. 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.

  13. UV/O3工艺去除甲基叔丁基醚过程中BrO3-的产生与控制%Bromate formation and control in process of removing methyl tert-butyl ether by UV/O3 technology

    Institute of Scientific and Technical Information of China (English)

    赵光宇; 吕锡武; 周易

    2013-01-01

    Bromate is a potential carcinogen and formed in treatment of bromide-containing water using ozone-based technologies.So,the study on bromate formation during removal of organic pollutions is necessary for applying UV/O3 process.The effects of water background,initial MTBE concentration,ozone dosage and dosing method on removal of methyl tert-butyl ether (MTBE) and formation of bromate were studied.Besides,the mechanism of action for ozone dosing method was explored.The results showed that MTBE removal rates obtained by UV/O3 process in ultrapure water and tap water were 93.5 % and 88.67%,and bromate concentration were 18.01 μg · L-1 and 12.13 μg· L-1,respectively,which were higher than the standard value of 10 μg · L-1.The promotion of initial MTBE concentration inhibited bromate formation,but longer reaction time were compulsory since MTBE concentration was required to be lower than proposed concentration of 5 μg · L-1.In this case,bromate formation was eventually enhanced.Increase of ozone dosage was favorable for MTBE removal,but caused decline of the utilization rate of ozone and the promotion of bromate formation.Comparing three ozone dosing methods in which the same ozone dosage of 5 mg · min · L-1 was applied,the highest hydroxyl radical (· OH) exposure and minimum ozone exposure were obtained in the method at ozone concentration of 0.75 mg · L-1 and reaction time of 120 min.Therefore,the concentrations of MTBE and bromate in water both met the standard values after treatment.

  14. 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

  15. 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.

  16. 村镇供水中臭氧消毒副产物溴酸盐生成规律研究%Study on formation law of byproduct——bromate during ozone disinfection for rural drinking water supply

    Institute of Scientific and Technical Information of China (English)

    贾燕南; 宋卫坤; 李晓琴; 胡孟; 刘文朝

    2013-01-01

    结合村镇供水特点,本文采取三种投加方式对9省63份作为饮用水水源的地下水水样进行臭氧投加试验,考察了不同地区的水样消毒后生成溴酸盐浓度水平的差异,研究了臭氧投加量、投加方式对溴酸盐生成浓度的影响.结果表明:原水溴离子浓度越低,pH值越低,投加臭氧后生成的溴酸盐量也较小;溴酸盐生成量与臭氧投加量在一定范围内呈线性正相关关系.同一投加量下,三种臭氧投加方式对应的溴酸盐生成量由小到大依次为:投加高浓度臭氧水、水射器投加、直接通入臭氧气体.%In accordance with the characteristics of rural drinking water supply, the ozone adding experiment on the groundwater samples from 63 water sources for the rural drinking water in 9 provinces is made with three ozone dosing methods, and then the difference among the levels of bromate concentrations formed after the disinfections of the water samples from various areas is investigated and the impacts from both the ozone dosing and the dosing method on the bromate forming concentration are studied.The result shows that the less the bromonium ion concentration of the raw water is, the lower the pH value is to be, and then the less content of the bromate formed after ozone adding is to be as well, while the bromate formation shows linear positive correlation with the ozone dosage with a certain range.Under an identical dosing, the bromate formations corresponded to the three o-zone dosing methods, i.e.adding high concentration ozone water, adding by water-jet, direct adding of ozone gas, vary in an order from less to large.

  17. 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).

  18. Determination of Bromate in Wheat Flour and Wheat Flour Products%小麦粉及小麦粉制品中溴酸盐的测定

    Institute of Scientific and Technical Information of China (English)

    陶大利; 苑向杰

    2012-01-01

    A method for determination of bromate in wheat flour and wheat flour products by Ion chromatography method is reported.The chromatographic column for DIONEX AS19(250mm×4.0mm),eluent(mobile phase) for KOH solution,Conductivity detector,extraced by pure water samples of bromate ion(BrO-3),RP(C18) column was used to remove the organic matter,the Ag/H column to remove sample extraction liquid disturbance in the chloride ion(Cl-),using ion chromatography conductivity detector for the determination,quantified by external standard method.Linear ranges of lutein was 0.05~2.0μg/mL,the linear equation was y=1.435x-0.031,relevant index R2=0.9998;Concentration in the 1.60mg/kg~4.80mg/kg range,the average recovery rate were 92.8~103.5%.%建立离子色谱法测定小麦粉及其小麦粉制品中溴酸盐的测定方法。采用的色谱柱为戴安的AS19(250×4.6mm),淋洗液(流动相)为KOH溶液。用纯水提取样品中溴酸根离子(BrO3-),经RP(C18)柱除去样品中得有机物,经Ag/H柱除去样品提取液中干扰氯离子(Cl-),采用离子交换色谱-电导检测器测定,外标法定量,经测试溴酸盐在0.05~2.0μg/mL范围内,线性良好,线性方程为y=1.435x-0.031,相关系数R=0.9998,添加浓度在1.60mg/kg~4.80mg/kg范围内,平均回收率在97.5%~98.4%之间。

  19. 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.

  20. 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.

  1. DISSCUSS ON CONTROL TECHNOLOGIES FOR THE CONTENT OF BROMATE FROM OZONATION DISINFECTION BY-PRODUCT IN DRINKING WATER%饮用水中臭氧消毒副产物溴酸盐含量的控制技术探讨

    Institute of Scientific and Technical Information of China (English)

    张书芬; 王全林; 沈坚; 钟雄华

    2011-01-01

    The paper described the formation mechanism of bromate in the process of ozonation, and then studied control method to limit the bromated content in drinking water in the steps of pretreatment of raw water, controlment of bromate formation and removal of bromated.It is a feasible approach to adopt membrane separation technology (control of raw water conductivity and microbial content), ammonia treatment, combination of various disinfectants and using new disinfectant, optimization of ozone disinfection process and activated carbon adsorption technology to control the bromate content in drinking water.In order to get the balance of ozone, microorganisms and bromate, water characteristic, production capacity,enterprise size and running cost should be concerned.%在阐述臭氧化过程中溴酸盐的生成机理的前提下,从原水预处理、溴酸盐形成过程控制、溴酸盐形成后消除3个阶段来分析研究控制饮用水中溴酸盐含量的方法.经过探讨和实践表明,采用膜分离技术(控制原水电导率和微生物含量)、加氨、采用新型消毒剂和多种消毒剂组合使用、优化臭氧消毒工艺和活性炭吸附技术等是较为可行的控制途径.饮用水生产企业根据水源特点,生产能力,企业规模、运行成本等条件进行选择尝试,从而实现臭氧,微生物和溴酸盐之间的平衡.

  2. 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.

  3. 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.

  4. 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.

  5. 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.

  6. 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.

  7. 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%.

  8. 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.

  9. Determination of Trace Nitrite and Bromate in Pure Water Samples by Ion Chroma Tography%离子色谱法测定饮用水中亚硝酸盐和溴酸盐含量的变化

    Institute of Scientific and Technical Information of China (English)

    李舒

    2011-01-01

    [目的]探讨饮用水中亚硝酸盐(NO2-)和溴酸盐(BrO3-)含量的变化.[方法]利用ICS-2000离子色谱法检测了3种饮用水中亚硝酸盐和溴酸盐在不同条件下的含量.[结果]在自来水、桶装纯净水、桶装矿泉水3种水中,亚硝酸盐含量随时间的增加有所增加,加热也未降低亚硝酸盐含量;纯水、自来水中未检测出溴酸盐,桶装矿泉水中测得的溴酸盐均随着时间的增加而增加,加热后能够较大程度上降低桶装矿泉水中溴酸盐的浓度.该方法检测的NO2-浓度在0~2 mg/L范围内有良好的线性关系(r=0.999 95),最小检测值为0.000 1 mg/L,实样加标回收率在97.34% ~ 108.61%;BrO3-浓度在0~2 mg/L范围内也有良好的线性关系(r=0.999 97),最小检测值为0.000 2 mg/L,实样加标回收率在95.93%~101.04%.[结论]该方法精密度高、操作简便、易推广.%[Objective] Changes of trace nitrite and bromate in pure water samples were explored. [ Method ] Contents of trace nitrite and bromate in three kinds of pure water samples under different conditons were determined by using ICS-2000 ion chromatography. [Result]The contents of nitrite in three samples of tap water,bottled water and bottled mineral water increased with the increase of time,but didn' t decrease under the treatment of heating. There was no bromate in pure water and tap water; the content of bromate in bottled mineral water also increased with the increase of time,and could be decreased to a much greater extent after healing. Nitrite showed good linear relationship within 0-2 mg/L (r = 0.999 95); the minimum detection value was 0.000 1 mg/L; and the sample standard addition was 97.34% - 108. 61%. Bromate also showed good linear relationship within 0 ~ 2 mg/L ( r = 0.999 97); the minimum detection value was 0.000 2 mg/L; and the sample standard addition was 95.93% ~ 101.04%. [ Conclusion]The method has high accuracy,simple operation and application.

  10. Photocatalytic Removal of Bromates with Noble Metal-Modified Titanium Dioxide%贵金属改性二氧化钛光催化去除溴酸盐

    Institute of Scientific and Technical Information of China (English)

    喻灵敏; 朱荣淑; 董文艺

    2014-01-01

    用浸渍法制备了各贵金属(包括Pt、Pd、Ru、Rh、Ir、Au、Ag)改性二氧化钛(M/TiO2)光催化剂,研究了紫外光下其光催化去除溴酸盐(BrO3-)活性。结果表明,Pt和高Ag量负载提高了TiO2光催化去除BrO3-活性,分别提高了4.6和2.9倍,Pt通过表面活性物种PtCl4的光敏化作用提高了其活性,而高负载量Ag通过与BrO3-还原产物Br-生成具有可见光活性的 AgBr 来提高其活性。Pd/TiO2、Ru/TiO2、Au/TiO2、Ir/TiO2、Rh/TiO2和低负载量的 Ag/TiO2,因不能有效提高 P25 TiO2光生电子与空穴的分离效率,反而可成为电子与空穴的复合中心,从而抑制了 TiO2光催化去除BrO3-活性。%TiO2 modified with nobel metals (M/TiO2, M = Pt, Pd, Ru, Rh, Ir, Au, Ag) was prepared by an impregnation method. The photocatalytic activity of M/TiO2 for bromate removal was studied under UV or visible light. The results show that high loading of Pt and Ag improves the photocatalytic activity of TiO2 on the removal of bromates up to 4.6 and 2.9 times, respectively. The photosensitization of the active species of the PtCl4 at the surface of Pt/TiO2 significantly improves the photocatalytic activity of TiO2. Ag mainly existed on the surface of TiO2 in the form of Ag0. During the photocatalytic removal process, Ag0 reacted with Br-to form AgBr with visible light activity. Similar to PtCl4, AgBr greatly improves the photocatalytic activity of TiO2 for bromate removal under visible light. However, Pd/TiO2, Ru/TiO2, Au/TiO2, Ir/TiO2, Rh/TiO2 and Ag/TiO2 with low Ag loading can not enhance the separation efficiency of photogenerated electron and hole, or generate the active species with visible activity directly or indirectly. These materials become the recombination centers of the charge carriers, thus inhibits the photocatalytic activity of TiO2 for bromate removal.

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

    Institute of Scientific and Technical Information of China (English)

    周虹; 周小新

    2009-01-01

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

  12. A Preliminary Study of the Formation of Bromate By-products During Ozone Disinfection in Rural Drinking Water Supply%农村供水臭氧消毒副产物溴酸盐生成的初步研究

    Institute of Scientific and Technical Information of China (English)

    贾燕南; 魏向辉; 刘文朝

    2013-01-01

    臭氧消毒近年来为各地农村供水工程所广泛采用,但其带来的副产物溴酸盐超标问题却没有引起足够的重视.对北京若干区县的实际水样进行臭氧投加试验,考察了副产物溴酸盐的生成情况,探讨了臭氧消毒的适用性.结果表明:北京地区地下水采用臭氧消毒时溴酸盐超标的风险较高,建议在选择臭氧消毒前首先对原水进行臭氧投加试验,并考察生成溴酸盐的浓度水平;臭氧投加方式对于溴酸盐生成量的影响较大.%Ozone disinfection is widely used in many rural drinking water supply projects. However, more attention should be paid to the fact that the bromate by-product formed may be over standard in the disinfection process. In this paper, ozone adding experiments towards groundwater samples of different rural drinking water projects from various towns in Beijing are developed, and the bromate formation of the water samples is observed. Results show that risk of bromate of theses groundwater samples from Beijing exceeding the standard values is rather high after ozone disinfection. Besides, ozone dosing methods has a significant effect on formation of bromate.

  13. 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.

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

    Institute of Scientific and Technical Information of China (English)

    窦艳艳; 杨丽莉; 徐荣; 胡恩宇

    2013-01-01

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

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

    Institute of Scientific and Technical Information of China (English)

    孙卫明; 孙建飞; 王权帅

    2013-01-01

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

  16. 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 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.

  17. Determination of rhenium by chrome black-T-sodium bromate catalytic kinetic spectrophotometry%铬黑T溴酸钠催化动力学分光光度法测定铼

    Institute of Scientific and Technical Information of China (English)

    王毅梦; 樊雪梅

    2015-01-01

    A new method combined with ultraviolet visible spectrophotometry was developed for the determination of rhenium which catalyzed the reaction of chrome black‐T‐sodium bromate. The dynamic conditions of the catalytic system was determined and the catalytic reaction apparent activation energy and the reaction rate constant were calculated ,respectively ,Ea=39.12 KJ/mol and K=1.248 × 10‐3/s. Under the optimal conditions ,the rhenium concentration showed a good linear relationship with the relative ab‐sorbance in the range of 0‐10.02 mg/L ,the detection limit was 2.7675 mg/L.%基于在硫酸介质中,铼催化溴酸钠氧化铬黑T的褪色反应,建立了测定铼的光度分析新方法。确定了催化体系的动力学条件,计算得出催化反应的表观活化能 Ea =39.12 KJ/mol ,反应速率常数为K =1.248×10-3/s。在选定的试验优条件下,铼的浓度在0~10.02 m g/L范围内与相对吸光度呈良好的线性关系,检出限为2.7675 m g/L。方法所用仪器简单,操作简便。

  18. 溴酸钾-基橙-铁试剂-(V)体系催化光度法测定痕量钒%A modified spectrophotometric determination of vanadium by catalysis of the methyl orange-tiron-bromate reaction

    Institute of Scientific and Technical Information of China (English)

    杨武; 张煊; 管飞

    2000-01-01

    讨论了在钛铁试剂活化下钒催化溴酸钾氧化甲基橙的最佳反应条件,建立了测定钒的新方法.在0.1mol·L-1H2SO4溶液中,506nm处监测反应,可测定0.1~100.0ng·mL-1范围的钒.方法检测下限可达30pg·mL-1,比文献方法提高了30余倍.用于铝合金及食品样中钒的测定,结果满意.%Conditions are described for improving the speed and sensitivity of a catalytic determination of vanadium.The reaction of methyl orange with potassium bromate using tiron as an activator at 0.1 mol·L-1 sulfuric acid and spectrophotometric measurement at 506 nm are recommended.Reagent concentration,reaction temperature and pH were studied in detail.The calibration curves are obtained over the range 0.1~100.0 ng·mL-1 of vanadium by fixed-time method and the detection limit was down to 30pg·mL-1,which was about 30 times better than the previous methods.The improved method was applied to determination of vanadium in aluminum alloy and food samples with satisfactory results.

  19. 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.

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

    Institute of Scientific and Technical Information of China (English)

    齐春华; 张颖; 王化勇

    2012-01-01

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

  1. 离子色谱法测定瓶(桶)装纯净水中痕量溴酸盐和亚硝酸盐的含量%IC Determination of Trace Amounts of Bromate and Nitrite in Bottled or Barrelled Purified Water

    Institute of Scientific and Technical Information of China (English)

    王洁; 谢晓烽; 陈英

    2012-01-01

    采用离子色谱法同时测定瓶(桶)装纯净水中溴酸盐和亚硝酸盐的含量。水样经AG19-4mm保护柱及DIONEX AS19色谱柱分离,以不同浓度的氢氧化钾溶液为淋洗液,溴酸盐和亚硝酸盐得到很好的分离。BrO3-和NO2-分别在5.00~100.00μg.L-1和1.00~50.00μg.L-1范围内呈线性,检出限(3s/k)分别为0.08,0.14μg.L-1。方法用于瓶(桶)装水中溴酸盐和亚硝酸盐的测定,加标回收率在92.7%~98.4%之间,相对标准偏差(n=5)均小于5.0%。%Contents of bromate and nitrite in bottle or barrelled purified water were determined by ion chromatography(IC).The protective column(AG19-4mm) and chromatographic column(DIONEX AS19) were used for separation,and KOH solutions of different concentrations were used as eluent.The bromate and nitrite were separated successfully.Linearity ranges of BrO3-and NO2-were found between 5.00-100.00 μg·L-1 and 1.00-50.00 μg·L-1,with detection limits(3s/k) of 0.08 and 0.14 μg·L-1 respectively.The proposed method was applied to the determination of BrO3-and NO2-in the samples of bottled or barrelled purified water,values of recovery found by standard addition method were in the range of 92.7%-98.4%,and RSD′s(n=5) were less than 5.0%.

  2. 大体积直接进样离子色谱法测定饮用水中痕量溴酸盐的方法研究%Determination of trace bromate in drinking water by Large volume direct injection ion chromatography method

    Institute of Scientific and Technical Information of China (English)

    杨国栋

    2012-01-01

    Objective:To establish a large volume direct injection ion chromatography method for conductivity detection of bro-mate in drinking water. Methods; Dionex ICS -20Q0 ion chromatography, EGC II KOH eluent generator, Dionex Ionpac AS19 analytical column, DS6 thermal conductivity detector and ASRS300 anion suppressor were involved in this method. The 10 mmol/L~35 mmol/L KOH was used for gradient elution at the flow rate of 1. 00 ml/min, and the injection volume was 500 ul. Results:It was obtained from the experiment that the correlation coefficient was 0.9999, precision was RSD < 2% , average recoveries were between 95.0% ~ 107% and the minimum detection limit was 5 ug/L. Conclusion; The method has the advantages of simple operation, rapidness, high sensitivity, good reproducibility, which can be used for the analysis of trace bro-roate in drinking water.%目的:建立一种大体积直接进样,电导检测饮用水中痕量溴酸盐的离子色谱分析法.方法:采用Dionex ICS -2000型离子色谱仪,EGCⅡKOH淋洗液自动发生器,10 mmol/L~ 35 mmol/L KOH梯度淋洗,流速1.00 ml/min,Dionex Ionpac AS19型分析柱,DS6型热电导检测器,ASRS300阴离子抑制器,进样体积500μl等分析条件.结果:经实验得到相关系数r =0.9999,精密度RSD <2%,平均加标回收率在95.0%~107%之间,方法的最低检出限为5μg/L.结论:该方法具有操作简单、快速、灵敏度高、重现性好等优点,可应用于饮用水中痕量溴酸盐的分析测定.

  3. 溴酸钾-苯酚红体系催化动力学光度法测定食品中的痕量甲醛%Determination of Trace Formaldehyde in Foods with Catalytic Kinetic Spectrophotometry in Potassium Bromate-Phenol Red System

    Institute of Scientific and Technical Information of China (English)

    严进

    2015-01-01

    A catalytic spectrophotometric method for the determination of trace formaldehyde is established based on the inhibitory effect of formaldehyde on the oxidation of phenol red by potassium bromate in H2SO4 medium. The optimum kinetic condition of the catalytic reaction has been investigated. The wavelength for the determination is 380 nm, and the linear range for determination of formaldehyde is 0.02~0.32 μg/mL with the detection limit of 6.10×10-9 g/mL.v The results from the studies suggest that the catalytic reaction is zero-or-der and the apparent activation energy of this reaction is 38.87 kJ/mol,and the apparent rate constant is k=9.1×10-4s-1. The procedure has been used to determine formaldehyde in foods, with the relative standard devi-ation of below 3.9%and the average recovery of 96.3 %~105.5 %. Results obtained by this method are con-sistent with the results found by the acetylacetone photometry.%基于溴酸钾在硫酸介质中可氧化苯酚红,甲醛的加入催化该氧化反应的进行,从而使溴酸钾氧化苯酚红的速度明显加快,据此建立了测定食品中痕量甲醛的新催化动力学分光光度法,并研究了该催化褪色反应的最佳动力学条件和参数。在测定波长380 nm下,测定方法的线性范围0.02~0.32滋g/mL,检出限为6.10×10-9 g/mL。催化反应为动力学零级反应,表现活化能为38.87 kJ/mol,催化反应速率常数k=9.1×10-4s-1。运用所建立的方法测定食品中痕量甲醛,相对标准偏差小于3.9%,回收率在96.3%~105.5%,表明该方法测得的结果与乙酰丙酮光度法所测结果一致。

  4. Simultaneous analysis of iodate,iodide,bromate and bromide by ion chromatography with ultraviolet detection%离子色谱-紫外检测法同时分析碘酸根、碘离子、溴酸根和溴离子

    Institute of Scientific and Technical Information of China (English)

    李朦; 于泓; 郑秀荣

    2014-01-01

    An analytical method of ion chromatography with ultraviolet detection has been developed and applied for the simultaneous determination of iodate,iodide,bromate and bro-mide. The separation was performed on a quaternary ammonium type anion exchange column with citric acid and acetonitrile as mobile phase. The effects of the detection wavelength,the kind and concentration of the mobile phase and other parameters on separation and detection of the four ions were investigated. The retention rules were studied and the chromatographic con-ditions were optimized. Under the conditions of 210 nm as detection wavelength,0. 9 mL / min as flow rate,40 ℃ as column temperature,and 1. 0 mmol / L citric acid-acetonitrile(85 :15,v /v;pH 5. 0)as mobile phase,the four ions were completely separated and the system peaks and other common anions didn’t interfere with the determination. The detection limits of the four ions(S / N = 3)were 0. 07 - 0. 16 mg / L. The relative standard deviations of the retention times and peak areas obtained by determining samples five times continuously were below 1% . The spiked recoveries of the four anions were from 98. 0% to 102% . This method has been success-fully used to determine ionic liquids synthesized by chemistry laboratory and underground water samples. The results were accurate and reliable.%建立了同时分析碘酸根、碘离子、溴酸根和溴离子的离子色谱-紫外检测分析方法。用季铵型阴离子交换柱,以柠檬酸-乙腈为流动相,采用紫外检测器实现了4种离子的同时分离和检测。研究了检测波长和流动相种类、浓度、pH 值等因素对4种离子分离和测定的影响,探讨了保留规律,优化了色谱分析条件。在检测波长为210 nm、流动相为1.0 mmol / L 柠檬酸-乙腈(85:15,v / v;pH 5.0)、流速为0.9 mL / min、柱温为40℃条件下,4种离子完全分离,且系统峰不干扰测定。4种离子的检出限(S / N =3)为0

  5. Fe-Al/Al2O3催化臭氧化去除水中有机污染物2,4-D过程中溴酸盐的生成控制研究%Inhibition of bromate formation during catalytic ozonation of organic pollutant 2,4-D in bromide-containing water over Fe-Al/Al2O3

    Institute of Scientific and Technical Information of China (English)

    李能能; 聂玉伦; 胡春

    2013-01-01

    Fe-Al supported on γ-Al2O3 (Fe-Al/Al2O3) was prepared via impregnation method followed by hydrolysis and hydrothermal treatment.Based on characterization of X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS),Fe3 + and Fe2 + coexisted-in Fe-Al/Al2O3 while Al was in the state of Al2O3 and AlOOH.In comparison with ozonation alone,the addition of Fe-A1/Al2O3 resulted in complete inhibition of BrO3-formation with higher efficiency for catalytic ozonation of 2,4-dichlorophenoxyacetic acid (2,4-D).Moreover,the catalyst could be reused for six times without significant loss of activity,indicating Fe-Al/Al2O3 has an excellent long-term stability.The effects of ozone dose and bromide concentration on TOC removal and bromate formation were also studied.The results showed that no significant bromate formation was found in catalytic ozonation process over FeAl/Al2O3 even with the increased ozone dose and bromide concentration,whereas the increase of ozone dose could result in higher TOC removal efficiency.%采用浸渍、强化水解和后续水浴加热的方法制得催化剂Fe-Al/Al2O3,并通过XRD和XPS等表征手段对其结构性能进行了研究.结果表明,催化剂中铁是以二价和三价存在,且以三价铁为主;铝则以Al2O3和AlOOH形态存在.与单独臭氧化相比,Fe-Al/Al2 O3既能高效矿化水中的难降解有机物2,4-二氯苯氧乙酸(2,4-D),又能明显抑制溴酸盐的生成,体现出很好的循环使用稳定性.进一步探讨了臭氧投加量和溴离子初始浓度对催化臭氧化效率和溴酸盐生成的影响.研究表明,在Fe-Al/Al2O3催化臭氧化过程中,水中溴酸盐浓度受臭氧投加量和溴离子初始浓度的影响较小,均可明显抑制溴酸盐的生成,且有机物的矿化效率随着臭氧投加量的增加而显著提高.

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

    DEFF Research Database (Denmark)

    Antoniou, Maria; Andersen, Henrik Rasmus

    2011-01-01

    limit of 10 μg/L. Depression of solution pH to 6.0, reduced BrO3- formation to half, but it was still well above the water limit. Pre-treatment with NH4+ also reduced BrO3- formation by approximately 50%, though it reduced atrazine degradation to 65%. Pre-treatment with Cl2/NH4+ reduced BrO3- formation......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...... for each pre-treatment. The required delivered O3 dose to achieve 90% removal of atrazine in the tap water from the DTU-campus was 3.5 mg/L which produced 130-170 µg/L BrO3-. Perozone did not reduce the required O3 dose for contaminant removal, however it limited BrO3- formation below the drinking water...

  7. 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.

  8. Substitute of potassium bromate%溴酸钾的替代物

    Institute of Scientific and Technical Information of China (English)

    岑涛

    2006-01-01

    介绍了溴酸钾等化学氧化剂在面包烘焙中的基本作用,以及酶制剂、乳化剂和非溴酸钾化学氧化剂替代溴酸钾的功能和非溴酸钾改良剂在面包焙烤实验中的效果.

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

    OpenAIRE

    2010-01-01

    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 o...

  10. 溴酸钾-藏红T光度法测定痕量亚硝酸根%Spectrophotometric determination of trace nitrite with potassium bromate and safranine T

    Institute of Scientific and Technical Information of China (English)

    李忠军; 崔宏伟; 熊良武

    2002-01-01

    研究了在磷酸介质中,由于亚硝酸根催化作用,溴酸钾能够氧化藏红T使之褪色,建立了测定痕量亚硝酸根的新方法,并探讨了这一催化反应的动力学条件.其线性范围为0~5.6 μg/L,检出限为2.0×10-8 g/L.用于纯净水中的亚硝酸根测定,结果满意.

  11. 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.

  12. Determination of trace silver by solid substrate-room temperature phosphorescence quenching method based on double catalytic system of meta-nitrophenyfluorone-polyoxyethylene-chromium-potassium bromate-β-cyclodextrin

    Science.gov (United States)

    Jiaming, Liu; Xuan, Lin; Aihong, Wu; Li-Xiang, Hu; Hangxia, HE; Honghua, Huang; Longdi, Li; Shaoqin, Lin

    2006-09-01

    A new solid substrate-room temperature phosphorescence (SS-RTP) quenching method for the determination of trace silver has been established. It is based on the fact that when using Mg 2+ as ion perturber and β-CD as surfactant, the system of meta-nitrophenyfluorone (R)-polyoxyethylene-Cr(III) can emit strong and stable room temperature phosphorescence signal on filter paper whose surface is modified by polyvinyl alcohol (PVA)-H 3BO 3-NaOH. Ag(I) can catalyze KBrO 3 oxidizing R-PEO-Cr(III) system which causes the quenching of SS-RTP. The reducing value of phosphorescence intensity (Δ Ip) is directly proportional to the concentration of Ag(I) in the range of 3.2-160 ag spot -1 (corresponding concentration: 2.43 fg ml -1, the sample volume: 0.40 μl spot -1) with a detection limit (LD) of 0.97 ag spot -1. The regression equation of working curve can be expressed as Δ Ip = 13.92 + 0.3089 m (ag spot -1) ( r = 0.9983, n = 6). This method has many advantages, such as a wide linear dynamic range, high sensitivity, good repeatability and selectivity. It has been applied to the determination of trace silver in real samples with satisfactory results. What is more, the mechanism of SS-RTP quenching method based on Ag(I) catalyzing KBrO 3 oxidizing meta-nitrophenyfluorone has also been discussed.

  13. 反相离子对液相色谱法测定小麦粉中的溴酸钾%Method of Potassium Bromate Determination in Wheat Flour by Ion-pair RP-HPLC

    Institute of Scientific and Technical Information of China (English)

    王骏; 张卉; 祝建华

    2007-01-01

    建立了反相离子对液相色谱法分离和测定小麦粉中的溴酸钾的方法.使用Symmetry shieldTM RP18色谱柱,以甲醇:4mmol/L柠檬酸+2mmol/L十六烷基三甲基溴化铵水溶液=48:52(V/V)为流动相,在220nm波长下检测.线性范围为:3.0~96.0mg/L,方法检出限为1.0mg/kg,方法回收率在89.7%~103.6%.

  14. Determination of trace rhodium by potassium bromate-safranine O inhibition kinetic spectrophotometry%溴酸钾-番红花红O阻抑动力学光度法测定痕量铑

    Institute of Scientific and Technical Information of China (English)

    张金宝

    2012-01-01

    在1.0 mol/L的硫酸介质和95℃热水浴中,痕量铑(Ⅲ)对KBrO3氧化番红花红O变色反应有很强的抑制作用,据此,建立了阻抑动力学光度法测定痕量铑(Ⅲ)的新方法并测定了有关动力学参数.在选定的试验条件下,方法的线性范围是0.2~0.8 ng/mL,检出限为1.93×10-11 g/mL,表观活化能为118.2 kJ/mol,阻抑反应对硫酸和铑都为一级反应.方法用于测定催化剂中铑,测定结果与SnCl2光度法的测定结果一致,相对标准偏差(RSD)为2.7%和2.9%.%In 1. 0 mol/L sulfuric acid medium and hot water bath at 95 °C , trace rhodium (Ⅲ) had strong inhibition action on the fading reaction of safranine O oxidized by KBrO3. Based on this, a new determination method of trace rhodium (Ⅲ) by inhibition kinetic spectrophotometry was established. Moreover, the related kinetic parameters were measured. Under the selected experimental conditions, the linear range of method was 0. 2 - 0. 8 ng/Ml, the detection limit was 1. 93×10-11 g/Ml, and the apparent activation energy was 118. 2 Kj/mol. The inhibition reaction was first order reaction for both sulfuric acid and rhodium. The proposed method was applied to the determination of rhodium in catalyst. The found results were consistent with those obtained by SnCl2 photometry. The relative standard deviations CRSD) were 2. 7% and 2. 9%.

  15. Control of Bromate of Drinking Water in Ozone Disinfection Process%饮用水臭氧消毒过程中溴酸盐含量的控制途径

    Institute of Scientific and Technical Information of China (English)

    刘长江; 贾娜; 韩梅

    2014-01-01

    本文论述了给水处理中溴酸根(BrO3-)的控制方法.BrO3-的生成与Br-初始浓度、臭氧投加量、水中天然有机物(NOM)的种类利浓度、有机碳浓度、以及水的pH值等多种因素有关.目前研究较多的削减BrO3-生成势的方法包括降低原水溴离子浓度、改变氯氨工艺、pH值、加氨(NH3)、加羟基自由基抑制剂、加过氧化氢(H2O2)以及多相催化臭氧氧化等多种方法.相比较而言,多相催化臭氧氧化方法克服了向水中投加化学试剂的主要缺点,副作用小,具有较好的发展前景.

  16. Detection of content of potassium bromate in wheat flour by reverse-titrate method%用反滴定法测定小麦粉中溴酸钾含量

    Institute of Scientific and Technical Information of China (English)

    罗力力; 向小黎; 李红敏; 陈霞; 姬勇

    2006-01-01

    采用反滴定测定小麦粉中溴酸钾的含量.研究了测定条件及干扰因素对测定的影响,并与AACC方法进行了比较.方法操作简单、灵活、实用,最低检出限0.01g/kg,标准偏差(S)小于0.56,相对标准偏差小于1.24%,回收率为:91.6%~95.2%.

  17. 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

  18. Interaction between gaseous ozone and crystalline potassium bromide

    Science.gov (United States)

    Levanov, A. V.; Maksimov, I. B.; Isaikina, O. Ya.; Antipenko, E. E.; Lunin, V. V.

    2016-07-01

    The formation of nonvolatile products of the oxidation of a bromide ion during the interaction between gaseous ozone and powdered crystalline KBr is studied. It is found that potassium bromate KBrO3 is the main product of the reaction. The influence of major experimental factors (the duration of ozonation, the concentration of ozone, the humidity of the initial gas, and the temperature) on the rate of formation of bromate is studied. The effective constants of the formation of bromate during the interaction between O3 and Br- in a heterogeneous gas-solid body system and in a homogeneous aqueous solution are compared.

  19. 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...

  20. 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.

  1. 40 CFR 141.64 - Maximum contaminant levels for disinfection byproducts.

    Science.gov (United States)

    2010-07-01

    ... in this paragraph (a): Disinfection byproduct Best available technology Bromate Control of ozone... source water: Disinfection byproduct Best available technology Total trihalomethanes (TTHM) and... disinfection byproducts. 141.64 Section 141.64 Protection of Environment ENVIRONMENTAL PROTECTION...

  2. 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.

  3. Catalytic Kinetic Potentiometry for the Determination of Trace Nitrite by the Potassium Bromate-Iodide System%溴酸钾-碘离子体系催化动力学电位法测定痕量亚硝酸根

    Institute of Scientific and Technical Information of China (English)

    刘金霞; 程伟; 孙炳耀

    2002-01-01

    实验中发现NO-2对KBrO3氧化I-的反应有很强的催化作用.可用碘离子选择电极跟踪反应过程,由此建立了测定痕量NO-2的新方法.在适宜条件下,该指示反应为一级反应,反应速度可用电位变化ΔE表示.当时间固定,ΔE与NO-2浓度在0~16×10-6 mol/L范围内呈线性关系,检出限为14×10-10 mol/L.该方法已用于肉类、蔬菜、粮食和血清中NO-2的测定,得到了可靠结果.

  4. 溴酸钾体系十二烷基苯磺酸钠动力学分光光度法测定食品中痕量铜(Ⅱ)%Determination of Trace Cu (Ⅱ) in Foods by Kinetic Spectrophotometry with Potassium Bromate-Sodium Dodecyl Benzene Sulfonate System

    Institute of Scientific and Technical Information of China (English)

    沈淑君; 李术艳

    2016-01-01

    研究了在表面活性剂十二烷基苯磺酸钠存在下,在pH=9.00的氨性缓冲溶液中,铜(Ⅱ)对溴酸钾氧化中性红褪色有明显的催化作用.通过测定595 nm下吸光度值的变化及其与铜(Ⅱ)浓度的线性关系,建立了分光光度法测定铜(Ⅱ)的新方法.方法的线性范围为0.012~0.12 μg/mL,线性方程为:△A=6.995c-0.0977,相关系数r=0.9992,检出限为7.74×10-10 g/mL.用于食品及水样中痕量铜的测定,结果令人满意,相对标准偏差(RSD,n=6)为1.8%~2.3%.

  5. Kinetic spectrophotometric determination of trace thallium(Ⅲ) based on the discoloring reaction of arsenazo M by oxidation of potassium bromate%溴酸钾氧化偶氮胂M褪色动力学光度法测定痕量铊(Ⅲ)

    Institute of Scientific and Technical Information of China (English)

    周之荣; 张纪文; 周瑜芬; 魏家文

    2006-01-01

    基于0.08 mol/LH2SO4介质中,痕量铊(Ⅲ)催化溴酸钾氧化偶氮胂M(AsAM)的褪色反应,建立了测定痕量铊(Ⅲ)的催化光度法.讨论了酸度、反应物浓度、反应温度、时间、干扰离子等因素的影响.研究了反应的最佳条件,并测定了一些动力学参数,催化反应的表观活化能为70.12kJ/mol.方法检出限为0.17μg/L,线性范围为0~20 μg/L.在25 mL溶液中,测定0.5μg铊(Ⅲ)的相对标准偏差为3.4%(n=11).结合溶剂萃取分离技术,用于测定废水及土壤样品中痕量铊(Ⅲ),回收率为97.0%~103.0%.

  6. Determination of trace formaldehyde by solid substrate-room temperature phosphorescence quenching method based on the rose bengal-potassium bromate-tween-80 system%固体基质室温燐光猝灭测定痕量甲醛

    Institute of Scientific and Technical Information of China (English)

    郑志勇

    2008-01-01

    基于R(HFinCl4I4)在滤纸同体基质上能发射强而稳定的室温燐光,KBrO3氧化R发生室温燐光猝灭,HCHO与KBrO3反应生成Br2进一步氧化R,导致室温燐光剧烈猝灭,HCHO含量△Ip值呈良好线性关系,据此建立了HFinCl4I4-KBrO3-Tween-80体系同体基质室温燐光猝灭测定痕量甲醛的新方法.加比不加Tween-80时,△Ip增大9.1倍.本方法的线性范围为0.016~1.6(fg/spot)(对应浓度为0.040~4.0pg/mL,0.40pL/spot),工作曲线回归方程△Ip=136.6+28.28mHCHO(fg/spot),n=6,相关系数r=0.9935,检出限为4.5ag/spot(对应浓度1.1x10-44g/mL),灵敏、简便、快速,用于实际样品中痕量甲醛的测定,结果满意.同时探讨了HFinCI4I4-KBrOy-Tween-80体系固体基质室温燐光猝灭法测定甲醛的反应机理.

  7. 饮用水臭氧消毒副产物——溴酸盐产生机理及影响因素研究进展%Research Advance of Mechanism and Influencing Factors About Ozone Disinfection By-product: Bromate in Drinking Water

    Institute of Scientific and Technical Information of China (English)

    刘利兵; 庞月红; 钱和; 姜雪

    2010-01-01

    随着饮用水安全问题的凸显,饮用水在臭氧消毒过程中产生的消毒副产物溴酸盐也引起了广大消费者的普遍关注.综述了臭氧消毒过程中溴酸盐的产生机理及其对人体健康的影响,并进一步阐述了影响消毒过程中溴酸盐产生的理化因素,为人们正确认识溴酸盐的危害,合理选择饮用水消毒方法和优化消毒工艺提供理论依据.

  8. 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.

  9. Analytic Solution of the Three-Variable Dynamical Equations of Oscillation Phenomena in B-Z Reaction

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The dynamical behaviour of the inorganic bromate oscillator catalyzed by manganese ions in the B-Z reaction is discussed, a three-variable nonlinear dynamical equations of the oscillation phenomena have been obtained, and an analytic solution and numerical results of the equations are given.

  10. 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.

  11. Efficient oxidative deprotection of trimethylsilyl, tetrahydropyranyl and methoxymethyl ethers under solvent-free conditions

    Institute of Scientific and Technical Information of China (English)

    Farhad Shirini; Saeideh Saeidi

    2008-01-01

    A mild, efficient and fast method for direct oxidation of trimethylsilyl, tetrahydropyranyl and methoxymethyl ethers to their corresponding carbonyl compounds using trinitratocerium (IV) bromate (TNCB) supported on NaHSO4·H2O under solvent-flee conditions is reported.

  12. 臭氧消毒水中溴酸盐生成及其控制

    Institute of Scientific and Technical Information of China (English)

    王文生; 陈存坤; 于晋泽; 纪海鹏; 贾凝

    2014-01-01

    Based on introducing the application of the technology of ozone disinfection on water treatment and food disinfection, the formation and influencing factors of bromate during the process of ozone disinfection are reviewed. The main factors influencing the formation of bromate are summarized,including the content of bromate in drinking water,ozone dosage and dosing mode,the temperature and pH value of water,ionic strength and the adding additive. The main ways that controls the formation of bromate are concluded.%在介绍臭氧消毒技术在饮用水处理及食品消毒中应用的基础上,对臭氧在水处理消毒杀菌过程中溴酸盐生成及影响因素进行综述;阐明影响溴酸盐生成的主要因素,包括原水中溴化物含量、臭氧投加量和投加方式、臭氧处理时水温及pH值、水中离子强度和投加催化剂等;总结控制溴酸盐生成的主要途径。

  13. Period-doubling and chaotic oscillations the ferroin-catalyzed Belousov-Zhabotinsky reaction in a CSTR

    Institute of Scientific and Technical Information of China (English)

    ZONG ChunYan; GAO QingYu; WANG YuMei; FENG JiaMin; MAO ShanCheng; ZHANG Lu

    2007-01-01

    The ferroin-catalyzed Belousov-Zhabotinsky (BZ) reaction, the oxidation of malonic acid by acidic bromate, is the most commonly investigated chemical system for understanding spatial pattern formation. Various oscillatory behaviors were found from such as mixed-mode and simple period-doubling oscillations and chaos on both Pt electrode and Br-ISE at high flow rates to mixed-mode oscillations on Br-ISE only at Iow flow rates. The complex dynamic behaviors were qualitatively reproduced with a two-cycle coupling model proposed initially by Gy(o)rgyi and Field. This investigation offered a proper medium for studying pattern formation under complex temporal dynamics. In addition, it also shows that complex oscillations and chaos in the BZ reaction can be extended to other bromate-driven nonlinear reaction systems with different metal catalysts.

  14. Period-doubling and chaotic oscillations in the ferroin-catalyzed Belousov-Zhabotinsky reaction in a CSTR

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The ferroin-catalyzed Belousov-Zhabotinsky(BZ) reaction,the oxidation of malonic acid by acidic bromate,is the most commonly investigated chemical system for understanding spatial pattern forma-tion. Various oscillatory behaviors were found from such as mixed-mode and simple period-doubling oscillations and chaos on both Pt electrode and Br-ISE at high flow rates to mixed-mode oscillations on Br-ISE only at low flow rates. The complex dynamic behaviors were qualitatively reproduced with a two-cycle coupling model proposed initially by Gy?rgyi and Field. This investigation offered a proper medium for studying pattern formation under complex temporal dynamics. In addition,it also shows that complex oscillations and chaos in the BZ reaction can be extended to other bromate-driven nonlinear reaction systems with different metal catalysts.

  15. A Novel Chemical Oscillator with Tyrosine as the Substrate

    Institute of Scientific and Technical Information of China (English)

    Wu YANG; Jie REN; Jin Zhang GAO; Hua YANG; Dong Yu Lü; Xiu Hui LIU

    2003-01-01

    A new chemical oscillating reaction system involving the manganese(II)-catalyzed reaction among potassium bromate, acetone and tyrosine in acidic medium was described in this paper. The apparent activation energy of the induction period (Ein) and that of oscillation period (Ep) were calculated, Ein=110.61KJ/mol, Ep=159.41KJ/mol. The optimum concentration of each reactant was investigated and a steady chemical oscillating system was obtained.

  16. An Investigation on Physical and Chemical Quality of Spring Waters

    Directory of Open Access Journals (Sweden)

    Fesem BAŞARI

    2010-12-01

    Full Text Available Objective: The aim of this study was to analyse the chemical and physical qualities of spring water coming to Water Chemistry Laboratory of Adana Hygiene Institute in 2009. The water quality parameters analysed were colour, flavor, odour, turbidity, conductivity, pH, iron, aluminum, boron, manganese, arsenic, ammonia, ozone and bromate. Method: The spring water samples coming to the laboratory, colour in 59 samples, flavor in 22 samples, odour in 57 samples, turbidity and bromate in 61 samples, pH in 63 samples, conductivity in 62 samples, aluminum and iron in 30 samples, boron in 15 samples, arsenic and manganese in 18 samples, ammonia in 60 samples, ozone in 48 samples were studied. ISO (International Organization for Standardization, DIN (Deutsches Institut für Normung, TS (Turkish Standard methods were used for study. The results evaluated according to criterion of ‘‘Regulation on the Quality of Water Intended for Human Comsumption’’.Results: As a result of physical analysis of spring water, turbidity was assigned in just two (%3,2 of 61 samples. pH and conductivity were studied in 63 and in 62 samples respectively and all the values were appropriate. Higher concentrations than the regulation limits were found for bromate in three samples (4,9 % of 61, and in one sample of respectively boron (6,7 % out of 15, manganese (5,6 % out of 18 and arsenic (5,6% out of 18. Aluminum, ammonia, iron and ozone values in the analized samples were not found over the limits.Conclusion: Being found of bromate rates high was related to ozonize. And found of boron, manganese and arsenic was a symptom of dangerous pollution in terms of health. So, spring water pollution control essential for public health.

  17. Post-Self-Assembly Cross-Linking to Integrate Molecular Nanofibers with Copolymers in Oscillatory Hydrogels

    Science.gov (United States)

    2013-05-09

    chemical reaction is the Belousov−Zhabotinsky (BZ) reaction, the bromate oxidation of an organic substrate catalyzed by a metal ion or metal complex.14...to tailor their properties and on understanding the correlation between molecular structure, chemical oscillation, and mechan- ical actuation. In our...Cationic Amphiphiles: Potent Antibacterial Agent. J. Phys. Chem. B 2010, 114, 4407−4415. Figure 8. Process for making type II hydrogels via self-assembly

  18. Monobromination of Activated Aromatic Compounds withPolyvinylbenzyltriphenylphosphonium Supported Tribromide

    Institute of Scientific and Technical Information of China (English)

    WU Ming-Hu; YANG Gui-Chun; CHEN Zu-Xing

    2001-01-01

    Chloromethylated crosslinked co-polyvinylbenzene-divinylber-zene (2% DVB) was treated with triphenylphospbhie and then with sodium bromate and hydrobromic acid to afford red col-ored insoluble polyvinylbenzyltriphenylphosphon supportedtribromide.This reagent could be used as a mild and efficient monobrominating reagent for activated aromatic compounds such as phenols,aromatic,aromatic amines and acety-lanilines with good yields and high para-selectivity.

  19. 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.

  20. 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...

  1. Facile and efficient aromatization of 1,4-dihydropyridines with M(NO3)2.XH2O, TNCB, TBAP and HMTAI and preparation of deuterium labeled dehydronifedipine from nifedipine-d3.

    Science.gov (United States)

    Shaikh, Ajam C; Chen, Chinpiao

    2010-06-15

    The easy and efficient aromatization of various 1,4-dihydropyridines was investigated using various metal nitrates, trinitratocerium(IV) bromate (TNCB), and tetrabutyl ammonium periodate (TBAP) as oxidant in acetic acid at 100 degrees C, as well as hexamethylenetetramine-iodine (HMTAI) reflux in methanol. The efficient conversion of nifedipine-d(3) to dehydronifedipine-d(3) as an internal standard can be used in the measurement of nifedipine concentration in a body.

  2. 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.

  3. AOPs with ozone and UV radiation in drinking water: contaminants removal and effects on disinfection byproducts formation.

    Science.gov (United States)

    Collivignarelli, C; Sorlini, S

    2004-01-01

    In this study, the advanced oxidation with ozone and UV radiation (with two low pressure UV lamps, at 254 and 185 nm wavelength) were experimented on a surface water in order to study the removal of two odorous compounds (geosmin and 2-methylisoborneol) and a pesticide (metolachlor), the influence on organic compounds (UV absorbance and THM precursors) and bromate formation. Different batch tests were performed with ozone concentration up to 10 mg/L, UV dose up to 14,000 J/m2 and a maximum contact time of 10 minutes. The main results show that metolachlor can be efficiently removed with ozone alone while for geosmin and MIB a complete removal can be obtained with the advanced oxidation of ozone (with concentration of 1.5-3 mg/L and contact time of 2-3 minutes) with UV radiation (with doses of 5,000-6,000 J/m2). As concerns the influence on the organic precursors, all the experimented processes show a medium removal of about 20-40% for UV absorbance and 15-30% for THMFP (trihalomethanes formation potential). As concerns bromate formation, the advanced oxidation of ozone/UV 254 nm shows a bromate formation that is about 40% lower with respect to conventional oxidation with ozone.

  4. 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.

  5. 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.

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

    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).

  7. 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.

  8. Implications of sequential use of UV and ozone for drinking water quality.

    Science.gov (United States)

    Meunier, Laurence; Canonica, Silvio; von Gunten, Urs

    2006-05-01

    The formation of bromate levels exceeding the drinking water standard of 10 microg L-1 may impose the reduction of ozone doses used in the treatment of drinking water. This paper illustrates the procedure of evaluating the use of reduced ozone doses while implementing an additional UV disinfection step for an actual drinking water treatment plant. Ozonation was performed at low ozone doses in bench-scale experiments with a pretreated river water from the Paris area (France). At the low ozone dose of 0.5 mg L-1, bromate formation could be kept below 0.4 microg L-1, while inactivation of vegetative bacteria and UV-resistant viruses was calculated to exceed 5 log units, and a substantial decoloration (31% of the absorption at lambda=254 nm) was achieved. Based on the measured transient ozone and OH radical concentrations, the oxidation of micropollutants was calculated. Fast reacting micropollutants containing phenol, amine or double bond moieties, such as sulfamethoxazole, diclofenac and 17-alpha-ethinylestradiol, were completely oxidized. Slow-reacting synthetic micropollutants, e.g., atrazine, iopromide and methyl tertiary butyl ether (MTBE), were oxidized by only 20%, 20% and 10%, respectively, and the taste and odor compounds 2-methylisoborneol (MIB) and geosmin by 40% and 50%, respectively. The addition of an UV treatment step to the existing treatment train, which should guarantee disinfection of ozone-resistant pathogenic microorganisms, including Cryptosporidium parvum oocysts, has negligible effects on water matrix components but may induce significant transformation of micropollutants. Overall, the combination of ozonation at reduced doses and UV treatment leads to an improved water quality with regard to disinfection, oxidation of micropollutants and minimization of bromate.

  9. Catalytic spectrophotometric determination of trace selenium in microemulsion after separation and enrichment by SDG

    Institute of Scientific and Technical Information of China (English)

    LI Huizhi; ZHAI Diantang; FAN Yingju

    2006-01-01

    A new catalytic spectrophotometric method was developed for the determination of trace amount of Se(Ⅳ) in microemulsion medium. The method is based on the catalytic effect of traces of Se(Ⅳ) on the oxidation of2',4'-dichlorophenylfluorone (p-CPF) by potassium bromate with HNO3 as an activator in the presence of nonionic microemulsion medium. Under optimum conditions, the calibration graph is linear in the range of 0.4-15 μg. L-1 of Se(Ⅳ) atseparated and enriched by sulphydryl dextrane gel (SDG). The method has been applied for determination of trace selenium with satisfactory results.

  10. 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)

  11. 40 CFR 372.65 - Chemicals and chemical categories to which this part applies.

    Science.gov (United States)

    2010-07-01

    ... iodide 74-88-4 1/1/87 Methyl isobutyl ketone 108-10-1 1/1/87 Methyl isocyanate 624-83-9 1/1/87 Methyl...-36-3 1/1/87 Potassium bromate 7758-01-2 1/1/95 Potassium dimethyldithiocarbamate 128-03-0 1/1/95 Potassium N-methyldithiocarbamate 137-41-7 1/1/95 Profenofos 41198-08-7 1/1/95 Prometryn 7287-19-6...

  12. 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

    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...... assay. There was an inverse association between age and DNA repair activity with a 0.65% decline in activity per year from age 18 to 83 (95% confidence interval: 0.16-1.14% per year). Univariate regression analysis also indicated inverse associations between DNA repair activity and waist-hip ratio (P...

  13. 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

  14. The role of Ce(III) in BZ oscillating reactions

    Science.gov (United States)

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

    2012-03-01

    Herein we present results on the oscillatory dynamics in the bromate-oxalic acid-acetone-Ce(III)/Ce(IV) system in batch and also in a CSTR. We show that Ce(III) is the necessary reactant to allow the emergence of oscillations. In batch, oscillations occur with Ce(III) and also with Ce(IV), but no induction period is observed with Ce(III). In a CSTR, no oscillations were found using a freshly prepared Ce(IV), but only when the cerium-containing solution was aged, allowing partial conversion of Ce(IV) to Ce(III) by reaction with acetone.

  15. 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.)

  16. Preozonation of bromide-bearing source water in south China

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    The effectiveness of preozonation was evaluated on treating a bromide-bearing dam source water in south China through batch-scale experiments. Preozonation at ozone doses of 0.5-1.0 mg/L (at ozone consumption base) enhanced total organic carbon(TOC) removal through coagulation, and resulted in an almost linear reduction of ultraviolet absorbance at 254 nm (UV254). The removals of TOC (after coagulation) and UV254 at the ozone dose of 1.0 mg/L were 36% and 70%, respectively. Preozonation at an ozone dose between 0.5 and 1.0 mg/L resulted in the removal of disinfection byproducts formation potential (DBFP) including trihalomethane formation potential (THMFP) and haloacetic acid formation potential (HAAFP) for about 50%. The removals of THMFP and HAAFP decreased with the further increase of ozone dose. Ozonation of bromide-bearing water (bromide concentration,34 μg/L) produced a bromate concentration under the detection limit(2 μg/L) at ozone doses < 1.5 mg/L. However, bromate >10 μg/L could be produced when the bromide concentration was increased to 96 μg/L.

  17. 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.

  18. Synthesis of α-Bromine- Terminated Polystyrene Macroinitiator and Its Initiation of MMA Polymerization by ATRP

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    In the present paper the synthesis of block copolymers via the transformation from living anionic polymerization (LAP) to atom transfer radical polymerization (ATRP) was described. Α-Bromine-terminated polystyrenes(PStBr) in the LAP step was prepared by using n-BuLi as initiator, tetrahydrofuran (THF) as the activator, α-methylstyrene (α-MeSt) as the capping group and liquid bromine (Br2) as the bromating agent. The effects of reaction conditions such as the amounts of α-MeSt, THF, and Br2 as well as molecular weight of polystyrene on the bromating efficiency (BE) and coupling extent (CE) were examined. The present results show that the yield of PStBr obtained was more than 93.8% and the coupling reaction was substantially absent. PStBr was further used as the macroinitiator in the polymerization of methyl-methacrylate(MMA) in the presence of copper(Ⅰ) halogen and 2,2-bipyridine(bpy) complexes. It was found that the molecular weight of the resulted PSt-b-PMMA increased linearly with the increase of the conversion of MMA and the polydispersity was 1.2-1.6. The structures of PStBr and P(St-b-MMA) were characterized by 1H NMR spectra.

  19. 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).

  20. Determination of UV active inorganic anions in potable and high salinity water by ion pair reversed phase liquid chromatography.

    Science.gov (United States)

    Sadiq Khan, Sadaf; Riaz, M

    2014-05-01

    Reversed phase column was dynamically modified into anion exchange column using various types of tetraalkylammonium salts as ion pair reagents (IPRs) for the separation and quantification of toxic anions such as nitrite, bromate, bromide and nitrate in potable and high salinity water. Various chromatographic parameters such as types and concentration of IPRs, concentration of organic modifier, phosphate buffer and mobile phase pH were optimized for the base-line separation of anions. The lowest detection limits (LDLs) were 0.2 for nitrate and nitrite, 0.6 µg ml(-1)for bromate and bromide respectively for potable water samples. NaCl and Na₂SO₄ were incorporated in the mobile phase for the analysis of high salinity water samples to minimize matrix interferences. This has resulted in change in elution order of anions, better tolerance of matrix anions such as chloride and sulphate. The developed method was successfully utilized for analysis of anions in potable, high salinity and sea water samples.

  1. Green synthesis of 5-bromo-vanillin%5-溴香兰素的绿色合成

    Institute of Scientific and Technical Information of China (English)

    彭安顺; 英荣建

    2009-01-01

    以冰醋酸为溶剂,香兰素为原料,AlBr3为催化剂,HBrO3与KBrO3为溴化剂合成了5-溴香兰素.采用正交实验法考察了影响收率的因素.最佳条件为:香兰素、KBrO3与AlBr3的物质的量的摩尔比为1:0.5:0.056,反应时间6.0h,反应温度30℃.在优化条件下收率可达90.4%.产物结构通过IR、1HNMR、熔点测定和元素分析得以确认.%5-bromo-vanillin was synthesizedby using vanillin as raw material,aluminium chloride as catalyst, hydrobromic acid and potassium bromate as brominating agent and acetic acid as solvent.Factors influencing the yield were investigated by the orthogonal experimental method.The optimum conditions are as follows:Vanillin: potassium bromate:aluminium chloride is 1mol:0.5mol:0.056mol, reaction time is 6.0h,reaction temperature is 30%. The yield is above 90.4% under the optimum conditions. The title compound was characterized by IR,1H NMR,mp. Measurement and element analysis.

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

    Science.gov (United States)

    Dansby-Sparks, Royce; Chambers, James Q; Xue, Zi-Ling

    2009-06-08

    An electrochemical technique has been developed for ultra-trace (ng L(-1)) vanadium (V) measurement. Catalytic adsorptive stripping voltammetry for V analysis was developed at mercury-coated gold micro-wire electrodes (MWEs, 100 microm) 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(-1) range (2 min deposition), with a detection limit of 0.88 ng L(-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(-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).

  4. UV-based advanced oxidation processes for the treatment of odour compounds: efficiency and by-product formation.

    Science.gov (United States)

    Zoschke, Kristin; Dietrich, Norman; Börnick, Hilmar; Worch, Eckhard

    2012-10-15

    The occurrence of the taste and odour compounds geosmin and 2-methyl isoborneol (2-MIB) affects the organoleptic quality of raw waters from drinking water reservoirs worldwide. UV-based oxidation processes for the removal of these substances are an alternative to adsorption and biological processes, since they additionally provide disinfection of the raw water. We could show that the concentration of geosmin and 2-MIB could be reduced by VUV irradiation and the combination of UV irradiation with ozone and hydrogen peroxide in pure water and water from a drinking water reservoir. The figure of merit EE/O is an appropriate tool to compare the AOPs and showed that VUV and UV/O(3) yielded the lowest treatment costs for the odour compounds in pure and raw water, respectively. Additionally, VUV irradiation with addition of ozone, generated by the VUV lamp, was evaluated. The generation of ozone and the irradiation were performed in a single reactor system using the same low-pressure mercury lamp, thereby reducing the energy consumption of the treatment process. The formation of the undesired by-products nitrite and bromate was investigated. The combination of VUV irradiation with ozone produced by a VUV lamp avoided the formation of relevant concentrations of the by-products. The internal generation of ozone is capable to produce ozone concentrations sufficient to reduce EE/O below 1 kWh m(-3) and without the risk of the formation of nitrite or bromate above the maximum contaminant level.

  5. 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.

  6. Acute and chronic toxicity of selected disinfection byproducts to Daphnia magna, Cyprinodon variegatus, and Isochrysis galbana.

    Science.gov (United States)

    Fisher, Daniel; Yonkos, Lance; Ziegler, Gregory; Friedel, Elizabeth; Burton, Dennis

    2014-05-15

    Ballast water treatment has become a major issue in the last decade due to the problem of invasive species transported and released by the uptake and discharge of ballast water for shipping operations. One of the important issues considering ballast water treatment is to determine whether treated ballast water, once discharged, is safe to the aquatic environment. The International Maritime Organization (IMO) Marine Environmental Protection Committee (MEPC) has determined that prior to approval of a ballast water management system, aquatic toxicity data must be available for both the active substance and relevant byproducts. Many proposed ballast water treatment systems use chlorine as the active ingredient. Although there are sufficient toxicity data concerning active substances such as chlorine, there are limited toxicity data concerning disinfection (halogenated) byproducts including dibromochloromethane, four haloacetic acids and sodium bromate. Acute and chronic toxicity were determined for these disinfection byproducts (DBPs). Acute toxicity values ranged from 96-h LC50s of 46.8 mg/l for Daphnia magna for both dibromochloromethane and sodium bromate to a 96-h LC50 of 376.4 mg/l for Cyprinodon variegatus for tribromoacetic acid. Acute Isochrysis galbana population growth effect values ranged from a 72-h EC10 of 39.9 mg/l for dichloroacetic acid to a 72-h EC50 of 15,954 mg/l for sodium bromate. Chronic toxicity mortality/reproduction effects values for D. magna ranged from a 21-d IC25 of 160.9 mg/l for tribromoacetic acid to a 21-d LOEC of 493.0 mg/l for trichloroacetic acid. Chronic toxicity mortality/growth values for C. variegatus ranged from a 32-d IC25 of 246.8 mg/l for trichloroacetic acid to a 32-d LOEC of 908.1 mg/l for tribromoacetic acid. I. galbana 96-h chronic population growth effects values ranged from an EC10 of 38.5 mg/l for trichloroacetic acid to an LOEC of 500.0 mg/l for tribromoacetic acid. Acute to chronic ratios for all of these

  7. 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).

  8. 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.

  9. Kinetic Determination of Uric Acid in Human Serum by Using the Uncatalyzed BZ Reaction in Non-equilibrium Steady State

    Institute of Scientific and Technical Information of China (English)

    Ren, Jie; Yang, Wu; Niu, Xiuli; Gao, Jinzhang

    2012-01-01

    A novel kinetic method for determination of uric acid in human serum by means of an uncatalyzed BZ system consisting of potassium bromate and p-hydroxybenzaldehyde (p-HBA) in sulfuric acid medium was proposed, in which the analyte perturbation to the system was recorded close to the bifurcation point. The potential change was directly proportional to the logarithm of concentration of uric acid in the range of 3.73 × 10 8--7.48 × 10-4 mol.L-1 (r=0.9983) with a detection limit of 7.45 × 10-9mol.L-I and a recovery from 98.9% to 101.1%. A comparison between the proposed technique and other methods indicated that results obtained were in agreement with those in clinical detection. In addition, the possible mechanism of action of uric acid on the uncatalyzed BZ reaction was also discussed briefly.

  10. 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.

  11. Sensitive Determination of Epinephrine Using Kinetic Spectrophotometric Method

    Directory of Open Access Journals (Sweden)

    Atefah Ekhtesasi

    2016-03-01

    Full Text Available In this study, thionine – bromate as a sensitive reaction system using kinetic spectrophotometric method for the determination of epinephrine is proposed. The method is based on the catalytic effect of epinephrine on the selected reaction system. The change in absorbance was followed spectrophotometrically as a criterion of the oxidation reaction progress. The effective reaction variables were optimized. Under optimized experimental conditions, calibration curve was linear over the range 0.4 – 12.8 mg/l and the detection limit was 0.13 mg/l for five replicate determinations of blank signal. The interfering effect of various species was also investigated. The developed procedure was successfully applied for the determination of diclofenac in pharmaceutical and biological samples satisfactorily.

  12. Inorganic-Organic Hybrid 18-Molybdodiphosphate Nanoparticles Bulk-modified Carbon Paste Electrode and Its Electrocatalysis

    Institute of Scientific and Technical Information of China (English)

    WANG,Xiu-Li(王秀丽); KANG,Zhen-Hui(康振辉); WANG,En-Bo(王恩波); HU,Chang-Wen(胡长文)

    2002-01-01

    A kind of inorganic- organic hybrid 18-molybdodiphosphate nanoparticles ([(C4H9)4N]6P2Mo18O62 @4H2O) was firstly used as a bulk-modifier to fabricate a three-dimensional chemically modified carbon paste electrode (CPE) by direct mixing. The electrochemical behavior of the solid nanoparticles dispersed in the CPE in acidic aqueous solution was characterized by cyclic and square-wave voltammetry. The hybrid 18-molybdodiphosphate nanoparticles bulk-modified CPE (MNP-CPE) displayed a high electrocatalytic activity towards the reduction of nitrite,bromate and hydrogen peroxide. The remarkable advantages of the MNP-CPE over the traditional polyoxometalates-modified electrodes are their excellent reproducibility of surface-renewal and high stability owing to the insolubility of the hybrid 18-molybdodiphosphate nanoparticles.

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

    Science.gov (United States)

    Hautman, D P; Bolyard, M

    1992-06-01

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

  14. [Investigation of the oxidation reaction of O3 with bromide ion in aqueous solution].

    Science.gov (United States)

    Yu, Xiao-Ting; Zhang, Jia-Hui; Pan, Xun-Xi; Zhang, Ren-Xi; Hou, Hui-Qi

    2012-09-01

    The reaction mechanism of O3 with bromide ion in aqueous solution was studied by ion chromatography and UV-Vis spectrometry instruments. Ion chromatography analysis showed that only 10% of Br- which was oxidized by ozone was formed into bromate ion. The results demonstrated that the final products of the oxidation reaction were identified as Br2 and Br3- except for BrO3-. The formation of Br3- which was yielded from the reaction of Br2 with Br- was the major process in the reaction of Br attacked by O3. The characteristic absorption spectrum of Br3- with an absorption peak at 260 nm was also investigated. The results may provide helpful information about the mechanism of the oxidation reaction of Br- with O3 and fate of Br- or its derivatives in the environment by the oxidation processes.

  15. 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.

  16. 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.

  17. Kinetic spectrophotometric determination of bromide in clidinium-c drug

    Institute of Scientific and Technical Information of China (English)

    Ali Sheibani; M. Reza Shishehbore; Zahra Tavakolian Ardakani

    2011-01-01

    A simple, rapid and sensitive method has been described for the determination of the trace amounts of bromide. The method is based on the catalytic effect of bromide ion on the oxidation of methylene blue by bromate in sulfuric acid media. The reaction is monitored spectrophotometrically by measuring the decrease in the absorbance of methylene blue at 665 nm. Bromide was determined in the range of 0.05-1.90 μg/mL with the detection limit of 0.03 μg/mL. The relative standard deviations of five replicate determinations of 0.20 and 10.0 μg/mL of bromide were 2.4% and 1.8%, respectively. The influence of potential interfering ions and substances was studied. The method is applied to the analysis of bromide in clidinium-c tablet as a real sample.

  18. 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.

  19. Use of a molecular beacon to track the activity of base excision repair protein OGG1 in live cells.

    Science.gov (United States)

    Mirbahai, Leda; Kershaw, Rachael M; Green, Richard M; Hayden, Rachel E; Meldrum, Rosalind A; Hodges, Nikolas J

    2010-02-01

    An abundant form of DNA damage caused by reactive oxygen species is 8-oxo-7,8-dihydroguanine for which the base excision repair protein 8-oxoguanine-DNA glycosylase 1 (OGG1) is a major repair enzyme. To assess the location and intracellular activity of the OGG1 protein in response to oxidative stress, we have utilised a fluorescence-quench molecular beacon switch containing a 8-oxo-dG:C base pair and a fluorescent and quencher molecule at opposite ends of a hairpin oligonucleotide. Oxidative stress was induced by treatment with potassium bromate. Flow cytometry demonstrated a concentration-dependent increase in the activity of OGG1 that was detected by the fluorescence produced when the oligonucleotide was cleaved in the cells treated with potassium bromate. This signal is highly specific and not detectable in OGG1 knock out cells. Induction of OGG1 activity is not a result of induction of OGG1 gene expression as assessed by qPCR suggesting a role for protein stabilisation or increased OGG1 catalytic activity. High resolution confocal microscopy pinpointed the location of the fluorescent molecular beacon in live cells to perinuclear regions that were identified as mitochondria by co-staining with mitotracker dye. There is no evidence of cut beacon within the nuclear compartment of the cell. Control experiments with a positive control beacon (G:C base pair and lacking the DAB quencher) did not result in mitochondrial localisation of fluorescence signal indicating that the dye does not accumulate in mitochondria independent of OGG1 activity. Furthermore, faint nuclear staining was apparent confirming that the beacon structure is able to enter the nucleus. In conclusion, these data indicate that the mitochondria are the major site for OGG1 repair activity under conditions of oxidative stress.

  20. Preparation and Electrocatalytic Application of Composites Containing Gold Nanoparticles Protected with Rhodium-Substituted Polyoxometalates

    Science.gov (United States)

    Wiaderek, Kamila M.; Cox, James A.

    2010-01-01

    Substitution of a metal center of phosphomolybdate, PMo12O403- (PMo12), or its tungsten analogue with dirhodium(II) and subsequent stabilization of gold nanoparticles, AuNPs, with Rh2PMo11 is demonstrated. The AuNP-Rh2PMo11 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-Rh2PMo11. At GC|APTES|AuNP-Rh2PMo11, cyclic voltammetry showed the expected set of three reversible peak-pairs for PMo11 in the range -0.2 to 0.6 vs (Ag/AgCl)/V and the reversible RhII,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|Rh2PMo11, and the electrocatalytic oxidation of methionine displayed characteristics of synergism between the AuNP and RhII. To stabilize AuNP-Rh2PMo11 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 × 10-8 mol dm-3. PMID:21499522

  1. Preparation and Electrocatalytic Application of Composites Containing Gold Nanoparticles Protected with Rhodium-Substituted Polyoxometalates.

    Science.gov (United States)

    Wiaderek, Kamila M; Cox, James A

    2011-04-01

    Substitution of a metal center of phosphomolybdate, PMo(12)O(40) (3-) (PMo(12)), or its tungsten analogue with dirhodium(II) and subsequent stabilization of gold nanoparticles, AuNPs, with Rh(2)PMo(11) is demonstrated. The AuNP-Rh(2)PMo(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(2)PMo(11). At GC|APTES|AuNP-Rh(2)PMo(11), cyclic voltammetry showed the expected set of three reversible peak-pairs for PMo(11) in the range -0.2 to 0.6 vs (Ag/AgCl)/V and the reversible Rh(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(2)PMo(11), and the electrocatalytic oxidation of methionine displayed characteristics of synergism between the AuNP and Rh(II). To stabilize AuNP-Rh(2)PMo(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 × 10(-8) mol dm(-3).

  2. Transformation of bromide in thermo activated persulfate oxidation processes.

    Science.gov (United States)

    Lu, Junhe; Wu, Jinwei; Ji, Yuefei; Kong, Deyang

    2015-07-01

    Sulfate radicals ( [Formula: see text] ) are applied to degrade various organic pollutants. Due to its high oxidative potential, [Formula: see text] is presumed to be able to transform bromide to reactive bromine species that can react with natural organic matter subsequently to form brominated products including brominated disinfection by-products (Br-DBPs). This research was designed to investigate the transformation of bromide in thermo activated persulfate oxidation process in the presence of humic acid (HA). Significant formation of bromoform and bromoacetic acids was verified. Their formation was attributed to the reactions of HA and reactive bromine species including Br·, [Formula: see text] HOBr(-), and free bromine resulted from the oxidation of bromide by [Formula: see text] . Yields of Br-DBPs increased monotonically at persulfate concentration of 1.0 mM and working temperature of 70 °C. However, the time-depended formation exhibited an increasing and the decreasing profile when persulfate was 5.0 mM, suggesting further degradation of organic bromine. HPLC/ICP-MS analysis demonstrated that the organic bromine was eventually transformed to bromate at this condition. Thus, a transformation scheme was proposed in which the bromine could be recycled multiple times between inorganic bromide and organic bromine before being finally transformed to bromate. This is the first study that reveals the comprehensive transformation map of bromine in [Formula: see text] based reaction systems, which should be taken into consideration when such technologies are used to eliminate contamination in real practice.

  3. 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.

  4. Fluorimeric analysis of bisphenol A based on carbon dots modified silica%基于碳量子点修饰硅胶荧光法测定塑料制品中的双酚A

    Institute of Scientific and Technical Information of China (English)

    任悦; 向国强; 张美然; 杨俊峰; 王帆

    2015-01-01

    Fluorimetric silica was prepared by carbon dots modifying silica .In hydrochloric acid medium ,the carbon dots could be oxided by potassium bromate .This could result in the fluo‐rescence quenching .However ,bisphenol A showed the inhibitory effect on the reaction of po‐tassium bromated oxidation of carbon dots .The fluorimertic method was just based on the in‐hibitory effect .The detection limit for bisphenol A was 5 2.μg · L -1 ,with a linear range of 20-500 μg · L -1 .The method was successfully applied for the determination of BPA in plastic products with a spiking recovery of 95% -104% .%制备了碳量子点修饰的硅胶SiO2@ CDs .在盐酸介质中KBrO3能够氧化碳量子点使其荧光发射峰减弱,而双酚A (BPA )对此氧化猝灭有明显抑制作用,据此建立了荧光法测定痕量双酚 A的新方法,线性范围是20~500μg·L -1,检出限3σ为52.μg·L -1.本文作者将该方法成功用于塑料制品中双酚A的测定,回收率在95%~104%之间.

  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. Disinfection by-products in ballast water treatment: an evaluation of regulatory data.

    Science.gov (United States)

    Werschkun, Barbara; Sommer, Yasmin; Banerji, Sangeeta

    2012-10-15

    To reduce the global spread of invasive aquatic species, international regulations will soon require reductions of the number of organisms in ballast water discharged by ships. For this purpose, ballast water treatment systems were developed and approved by an international procedure. These systems rely on established water treatment principles which, to different degrees, have been proven to generate disinfection by-products with hazardous properties but have only scarcely been investigated in marine environments. Our study evaluates the publicly available documentation about approved ballast water treatment systems with regard to by-product formation. The most commonly employed methods are chlorination, ozonation, and ultraviolet (UV) irradiation. Chlorination systems generate trihalomethanes, halogenated acetic acids, and bromate in substantially larger quantities than reported for other areas of application. Levels are highest in brackish water, and brominated species predominate, in particular bromoform and dibromoacetic acid. Ozonation, which is less frequently utilized, produces bromoform in lower concentrations but forms higher levels of bromate, both of which were effectively reduced by active carbon treatment. In systems based on UV radiation, medium pressure lamps are employed as well as UV-induced advanced oxidation. For all UV systems, by-product formation is reported only occasionally. The most notable observations were small increases in nitrite, hydrogen peroxide, halogenated methanes and acetic acids. The assessment of by-product formation during ballast water treatment is limited by the lacking completeness and quality of available information. This concerns the extent and statistical characterisation of chemical analysis as well as the documentation of the test water parameters.

  7. 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.

  8. VARIATION OF DISINFECTION BYPRODUCTS(DBPs)IN THE WATER PLANT USING PRE-OZONATION TREATMENT%水厂预臭氧化处理过程中消毒副产物的变化研究

    Institute of Scientific and Technical Information of China (English)

    李思思; 何凤华; 钟晓; 孙淑琴; 翟利芳; 王启山

    2012-01-01

    Study on the variation of disinfection byproducts (DBPs) in a water plant, which treated Luan River by preozonalion-UV+chlorine disinfection technics. THMFP. HAAFP, fonnaldehyde, and bromate in effluent water were detected. The results showed that preozonation can reduce THMFP and HAAFP, the average removal rate were 22.76% and 2238% separately; and it reached up to 46.23% and 55.38% after the whole processes. Though the concentration of fonnaldehyde increased after treated by pre-ozonation, it was significantly reduced in the following process. No bromate was detected in the effluent water.%以滦河水为处理对象,对天津市某水厂预臭氧化-紫外+氯联合消毒工艺处理过程中的氯化消毒副产物和臭氧副产物的变化情况进行了分析研究.分别对各处理单元出水中的三卤甲烷生成势(THMFP)、卤乙酸生成势(HAAFP)、甲醛、溴酸盐的含量进行检测.结果表明,原水经过预臭氧化处理后,THMFP和HAAFP的质量浓度均有降低,预臭氧处理单元对THMFP和HAAFP的平均去除率分别为22.76%和22.38%;整套工艺对THMFP和HAAFP的平均去除率分别可达46.23%和55.38%.经预臭氧化处理后,甲醛的浓度上升,但后续工艺对甲醛的去除效果较好,未出现溴酸盐超标.

  9. pH oscillations in the BrO3--SO3(2-)/HSO3- reaction in a CSTR.

    Science.gov (United States)

    Szantó, Tibor G; Rabai, Gyula

    2005-06-23

    Large-amplitude pH oscillations have been measured during the oxidation of sulfur (IV) species by the bromate ion in aqueous solution in a continuous-flow stirred tank reactor in the absence of any additional oxidizing or reducing reagent. The source of the oscillation in this simple chemical reaction is a two-way oxidation of sulfur (IV) by the bromate ion: (1) the hydrogen-ion-producing self-accelerating oxidation to sulfur (VI) (SO4(2-)), and (2) a hydrogen-ion-consuming oxidation to sulfur (V) (S2O6(2-)). In such a way, both the H+-producing and H+-consuming composite processes required for a pH oscillator take place in parallel in a reaction between two reagents in this system. A simple reaction scheme, consisting of the protonation equilibria of SO3(2-) and HSO3-, the oxidation of HSO3- and H2SO3 by BrO3- to SO4(2-), and the oxidation of H2SO3 to S2O6(2-) has successfully been used to simulate the observed dynamical behavior. Simulation with this simple scheme shows that oscillations can be calculated even if only about 1% of sulfur (IV) is oxidized to S2O6(2-) along with the main product SO4(2-). Agreement between calculated and measured dynamical behavior is found to be quite good. Increasing temperature decreases both the period length of oscillations in a CSTR and the Landolt time measured in a closed reactor. No temperature compensation of the oscillatory frequency is found in this reaction.

  10. pH-Controlled assembly of two novel Dawson-sandwiched clusters involving the in situ reorganization of trivacant α-[P2W15O56](12-) into divacant α-[P2W16O57](8.).

    Science.gov (United States)

    Guo, Ling-Yu; Jagodič, Marko; Zeng, Su-Yuan; Wang, Zhi; Shi, Zhi-Qiang; Wang, Xing-Po; Tung, Chen-Ho; Sun, Di

    2016-05-28

    Modified classical trivacant Wells-Dawson α-[P2W15O56](12-) and the assembly of related sandwiched transition metal clusters are of interest, but surprisingly few reports of these materials exist because of the sensitivity of α-[P2W15O56](12-) to the assembly environment. Herein, we describe the pH-controlled assembly of two novel Dawson-sandwiched clusters, (H2bpz)6[Co2(P2W16O57)2]·22H2O (1, bpz = 3,3',5,5'-tetramethyl-4,4'-bipyrazole) and (H2bpz)6[Co3H2(P2W16O57)(P2W15O56)(H2O)]·12H2O (2), involving the in situ transformation of α-[P2W15O56](12-). Both clusters were characterized by X-ray single-crystal diffraction, FT-IR spectroscopy, UV-Visible spectroscopy, thermogravimetric analysis, powder X-ray diffraction, and elemental analyses. X-ray crystallography showed that both heteropolytungstates become divacant α-[P2W16O57](8-) and symmetrically encapsulate two edge-shared CoO6 octahedra in the interior in 1, while only one divacant α-[P2W16O57](8-) is observed in 2, which combined with another trivacant α-[P2W15O56](12-) to asymmetrically clamp three edge-shared CoO6 octahedra. The α-[P2W16O57](8-) heteropolytungstate should be generated in situ from α-[P2W15O56](12-)via self-decomposition equilibria in solution. Their electrochemical behaviors reveal characteristic multi-electron redox processes related to W(VI) centers. The electrocatalytic reduction performances toward nitrite, hydrogen peroxide, chlorate, bromate and iodate were fully measured and discussed; among these species, both clusters exhibit the best electrocatalytic activity towards the reduction of bromate. Magnetic measurements indicate weak ferromagnetic exchange interactions between Co atoms sandwiched by vacant polyoxometalates.

  11. 3种填料有机物和氨氮去除性能及吸附效果比较%ORGANIC MATTER AND AMMONIA REMOVAL AND ADSORPTION ABILITY OF THREE KINDS OF CARRIERS

    Institute of Scientific and Technical Information of China (English)

    李朋; 汪群慧; 郑天龙; 谢维民

    2012-01-01

    Study on the variation of disinfection byproducts (DBPs) in a water plant, which treated Luan River by preozonalion-UV+chlorine disinfection technics. THMFP. HAAFP, fonnaldehyde, and bromate in effluent water were detected. The results showed that preozonation can reduce THMFP and HAAFP, the average removal rate were 22.76% and 2238% separately; and it reached up to 46.23% and 55.38% after the whole processes. Though the concentration of fonnaldehyde increased after treated by pre-ozonation, it was significantly reduced in the following process. No bromate was detected in the effluent water.%考察了海绵球形填料、螺旋形填料和纤维球填料的处理效果及吸附性能.结果表明,常温低填充比(15~20℃,13.75%)时,螺旋形填料COD平均去除率最高,可达到97%以上,3种填料氨氮平均去除率均可达到99%以上.海绵球形填料受填充比影响较小,而填充比过高会影响螺旋形填料和纤维球填料的传质布气效果.纤维球具有巨大的比表面积,吸附性能较强,单位体积附着污泥量可达22.97 g/L,且其吸附性能受温度影响小.螺旋形填料单位比表面积附着污泥量为0.042g·m3/m2,其吸附性能与其表面电荷和构型有关.海绵球形填料单位质量填料附着污泥量高,在相同要求下需要填料质量小,运输和安装时可节约成本.

  12. 预臭氧化工艺对消毒副产物影响的生产性研究%Full-scale study on effects of pre-ozonation on disinfection by - products

    Institute of Scientific and Technical Information of China (English)

    岳尚超; 王启山; 张伟林; 李思思; 张怡然; 刘艳芳; 鲁金凤; 赵文玉

    2012-01-01

    通过进行预臭氧化一紫外线联合氯消毒工艺处理高温高藻期滦河水的生产性试验,检测和分析三卤甲烷生成势(THMFP)和卤乙酸生成势(HAAFP)的含量变化情况,研究了整套水处理工艺,尤其是预臭氧化单元对氯消毒副产物(DBPs)的去除效果.同时,研究了甲醛和溴酸盐这两种臭氧化副产物在处理过程中的生成情况.结果表明:在高温高藻期,预臭氧化单元对THMFP和HAAFP的平均去除率分别为12.43%和15.06%,整套工艺对THMFP和HAAFP的平均总去除率分别为39.33%和54.12%,氯消毒副产物前体物得到有效去除;出水中甲醛含量低于50μg/L,溴酸盐的含量小于6μg/L,臭氧氧化副产物得到了有效控制.%A full-scale study was done on the processes of pre-ozonation and a combination disinfection of ultraviolet and chlorine to treat the Luan River raw water in high temperature and high algae concentration phase. Through the testing and analyzing of the trihalomethanes formation potential (THMFP) and haloacetic acids formation potential (HAAFP) variances, the whole set of water treatment process was studied, especially the effects of pre-ozonation on disinfection byproducts (DBPs) removal. At the same time, the formation of formaldehyde and bromated in treatment process was also studied. The results showed: during high temperature and high algae concentration period, the average removal rates of THMFP and HAAFP by pre-ozonation were 12. 43% and 15. 06% respectively, and the removal rates of combined process were 39. 33% and 54. 12% respectively, which meant the precursors of DBPs were removed effectively; formaldehyde and bromate in effluent were less than 50 μg/L and 6 μg/L respectively, which meant the DBPs were also controlled effectively.

  13. Cloud point extraction of plutonium in environmental matrixes coupled to ICPMS and α spectrometry in highly acidic conditions.

    Science.gov (United States)

    Labrecque, Charles; Whitty-Léveillé, Laurence; Larivière, Dominic

    2013-11-01

    A new cloud point extraction procedure has been developed for the quantification of plutonium(IV) in environmental samples. The separation procedure can be either coupled to inductively coupled plasma mass spectrometry (ICPMS) or α spectrometry for plutonium quantification. The method uses a combination of selective ligand (P,P'-di(2-ethylhexyl) methanediphosphonic acid (H2DEH[MDP])) and micelle shielding by bromine formation to enable quantitative extraction of Pu in highly acidic solutions. Cross-optimization of all parameters (nonionic and ionic surfactant, chelating agent, bromate, bromide, and pH) led to optimal of the extraction conditions. Figures of merit of the method for the detection using α spectrometry and ICPMS are reported (limit of detection, limit of quantification, minimal detectable activity, and recovery). Quantitative extractions (>95%) were obtained for a wide variety of aqueous and digested samples (synthetic urine, wastewater, drinking water, seawater, and soil samples). The method features the first successful coupling between α spectrometry and cloud point extraction and is the first demonstration of CPE suitability with metaborate fusion as a sample preparation approach, techniques used extensively in nuclear industries.

  14. Determinination of Trace Formaldehyde by Methyl Orange Polarography%甲基橙极谱法测定痕量甲醛

    Institute of Scientific and Technical Information of China (English)

    戴丽艳

    2014-01-01

    The existence of trace formaldehyde had a strong catalytic effect on the reaction of potassium bromate oxidation of methyl orange in the dilute sulphuric acid medium.Methyl orange and their oxidation products could produce sensitive polarographic adsorptive wave in the dropping mercury electrode. In this article the change of the concentration of methyl orange in the process of catalytic reaction was determined by the polarography. And the determination of trace formaldehyde was established by the kinetics of catalytic polarography method.%稀硫酸介质中,痕量甲醛的存在对溴酸钾氧化甲基橙的反应有很强的催化作用。而甲基橙及其氧化产物均能在滴汞电极上产生灵敏的极谱吸附波。本文以极谱法测定催化反应过程中甲基橙浓度的变化,建立了催化动力学极谱法测定痕量甲醛的方法。

  15. 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.

  16. Exposure to mutagenic disinfection byproducts leads to increase of antibiotic resistance in Pseudomonas aeruginosa.

    Science.gov (United States)

    Lv, Lu; Jiang, Tao; Zhang, Shenghua; Yu, Xin

    2014-07-15

    Bacterial antibiotic resistance (BAR) in drinking water has become a global issue because of its risks on the public health. Usually, the antibiotic concentrations in drinking water are too low to select antibiotic resistant strains effectively, suggesting that factors other than antibiotics would contribute to the emergence of BAR. In the current study, the impacts of mutagenic disinfection byproducts (DBPs) on BAR were explored, using four typical DBPs: dibromoacetic acid, dichloroacetonitrile, potassium bromate, and 3-chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone (MX). After exposure to DBPs, resistances to 10 individual antibiotics and multiple antibiotics were both raised by various levels, norfloxacin and polymycin B resistances were enhanced even greater than 10-fold compared with control. MX increased the resistance most observably in the selected DBPs, which was consistent with its mutagenic activity. The resistant mutants showed hereditary stability during 5-day culturing. The increase of BAR was caused by the mutagenic activities of DBPs, since mutation frequency declined by adding ROS scavenger. Mutagenesis was further confirmed by sequencing of the related genes. Our study indicated that mutagenic activities of the selected DBPs could induce antibiotic resistance, even multidrug resistance, which may partially explain the lack of agreement between BAR and antibiotic levels in drinking water.

  17. Interaction of ozone and carbon dioxide with polycrystalline potassium bromide and its atmospheric implication

    Science.gov (United States)

    Levanov, Alexander V.; Isaikina, Oksana Ya.; Maksimov, Ivan B.; Lunin, Valerii V.

    2017-03-01

    It has been discovered for the first time that gaseous ozone in the presence of carbon dioxide and water vapor interacts with crystalline potassium bromide giving gaseous Br2 and solid salts KHCO3 and KBrO3. Molecular bromine and hydrocarbonate ion are the products of one and the same reaction described by the stoichiometric equation 2KBr(cr.) + O3(gas) + 2CO2(gas) + H2O(gas) → 2KHCO3(cr.) + Br2(gas) + O2(gas). The dependencies of Br2, KHCO3 and KBrO3 formation rates on the concentrations of O3 and CO2, humidity of initial gas mixture, and temperature have been investigated. A kinetic scheme has been proposed that explains the experimental regularities found in this work on the quantitative level. According to the scheme, the formation of molecular bromine and hydrocarbonate is due to the reaction between hypobromite BrO-, the primary product of bromide oxidation by ozone, with carbon dioxide and water; bromate results from consecutive oxidation of bromide ion by ozone Br- → +O3 , -O2 BrO- → +O3 , -O2 BrO2- → +O3, -O2 BrO3- .

  18. Switching the BZ reaction with a strong-acid-free gel.

    Science.gov (United States)

    Hara, Yusuke; Yamaguchi, Yoshinori; Mayama, Hiroyuki

    2014-01-16

    In the present study, a novel gel with a semi-interpenetrating polymer network (semi-IPN) that undergo the Belousov-Zhabotinsky (BZ) reaction without the addition of a strong acid (HNO3 or H2SO4) was developed. The required concentrations of the BZ substrates, sodium bromate (NaBrO3) and malonic acid (MA), under these conditions were higher than under the normal BZ reaction conditions, involving the addition of a strong acid. The period of the BZ reaction with the novel gel (semi-IPN BZ gel) decreased with increasing concentrations of NaBrO3 and MA. Moreover, the connection of the semi-IPN BZ gel to a conventional BZ gel facilitated the reaction in the latter through the propagation of the intermediates from the former to the latter. The BZ reaction stopped when the conventional BZ gel was disconnected from the semi-IPN BZ gel. These results demonstrate that the BZ reaction in the conventional BZ gel underwent on-off switching, controlled by its attachment to the semi-IPN BZ gel. This on-off switching mechanism would be valuable in controlling actuators and robots without strong acids.

  19. New Inorganic-organic Hybrid Compound Containing One Dimensional Keggin Polyoxometalate[SiW11O39Co]6- Chains:Preparation,Characterization and Application in Chemically Bulk-modified Electrode

    Institute of Scientific and Technical Information of China (English)

    WANG Xiu-li; LIN Hong-yan; LIU Guo-cheng; CHEN Bao-kuan; BI Yan-feng

    2008-01-01

    A new inorganic-organic hybrid compound based on polyoxometalate and organic ligand formulated as (H2bpp)3[SiW11O39Co]~2H2O(1)[bpp=1,3-bis(4-pyridyl)propane]was hydrothermally synthesized and structurally characterized by elemental analysis,single-crystal X-ray diffraction,IR,TG,and cyclic voltammetry.Single-crystal X-ray diffraction analysis reveals that compound 1 consists of interesting cobalt-monosubstituted POMs one dimensional chain together with protonated bpp ligands.Additionally,the polyoxoanions combined with the discrete organic substrates by hydrogen bond interactions to afford a supramolecular 3D network structure.The hybrid compound 1 was used as a bulk modifier to fabricate a three-dimensional chemically modified carbon paste electrode(1-CPE)by direct mixing.The electrochemical behavior and electrocatalysis of 1-CPE were studied in detail.The results indicate that 1-CPE has good electrocatalytic activities toward the reduction of nitrite or bromate in 1mol/L H2SO4 aqueous solution.1-CPE shows remarkable stability that can be ascribed to the insolubility of compound 1 and the supramolecular interactions existed between 1D POM anion chains and organic ligand bpp,which is very important for practical applications in electrode modification.

  20. New Inorganic-organic Hybrid Tetravanadate:Preparation, Characterization and Application in Chemically Modified Electrode

    Institute of Scientific and Technical Information of China (English)

    SUN Ying-hua; LI Xiao-ping; MEI Ze-min; ZHU Yu; NIU Li

    2011-01-01

    A new inorganic-organic hybrid tetravanadate [Co(2,2'-bpy)3]2V4O12.llH2O(l) has been prepared and characterized. X-Ray diffraction study reveals that compound 1 contains classical cluster anions [V4O12]4-, coordi nated cations [Co(2,2'-bpy)3]2+ and eleven water molecules, in which an interesting decamer water cluster is formed.The hybrid nanoparticles were firstly used as a bulk-modifier to fabricate a chemically modified paste electrode (1-CPE). The electrochemical behavior and electrocatalysis of 1-CPE have been studied in detail. The results indicate that 1-CPE has a good electrocatalytic activity toward the reduction of bromate in a 0.5 mol/L H2SO4 aqueous solu tion. I-CPE shows remarkable stability that be ascribed to the hydrogen bonding interactions between V4O12 cluster and water cluster, which are very important for practical application in electrode modification.

  1. Oscillating chemiluminescence in rhodamine B-induced Belousov-Zhabotinsky reaction catalyzed by Ce(Ⅳ)

    Institute of Scientific and Technical Information of China (English)

    DUAN ChunFeng; LIU GuangMing; ZHANG ZhiFeng; CUI Hua

    2009-01-01

    It was found that rhodamine B could induce oscillating chemiluminescence (OCL) from the Ce4+-cata-lyzed Belousov-Zhabotinsky reaction. This new OCL system, i.e., rhodamine B-malonic acid-bromate-Ce(IV)-sulfuric acid, exhibited two clearly distinguished emission peaks in each oscillation period. The initial concentrations of the reactants strongly influenced the oscillation pattern. For the study of the CL mechanism, a platform for a versatile and simultaneous potential and CL measurement was estab-lished to compare the potential oscillation with the CL oscillation behavior of this system. The CL spectra, UV-visible absorption spectra and time-resolved fluorescence spectra of this OCL system were studied. A possible, simplified mechanism for the OCL is proposed. It is suggested that the generation of the two CL peaks is likely due to the oxidation of the intermediate of rhodamine B by Co(IV) and Br2, respectively. This work provided a new method and platform to research the complex chemical oscilla-tions.

  2. Controlling various contaminants in wastewater effluent through membranes and engineered wetland

    Institute of Scientific and Technical Information of China (English)

    Sarper SARP; Sungyun LEE; Noeon PARK; Nguyen Thi HANH; Jaeweon CHO

    2009-01-01

    For effective wastewater reclamation and water recovery, the treatment of natural and effluent organic matters (NOM and EfOM), toxic anions, and micropollutants was considered in this work. Two different NOM (humic acid of the Suwannee River, and NOM of US and Youngsan River, Korea), and one EfOM from the Damyang wastewater treatment plant, Korea, were selected for investigating the removal efficiencies of tight nanofiltration (NF) and ultrafiltration (UF) membranes with different properties. Nitrate, bromate, and perchlorate were selected as target toxic anions due to their well known high toxicities. Tri-(2-chloroethyl)-phosphate (TCEP),oxybenzone, and caffeine, due to their different Kow and pKa values, were selected as target micropollutants. As expected, the NF membranes provided high removal efficiencies in terms of all the tested contaminants, and the UF membrane provided fairly high removal efficien-cies for anions (except for nitrate) and the relatively hydrophobic micropollutant, oxybenzon. Through the wetlands, nitrate was successfully removed. Therefore, a fair process of combining membranes with an engineered wetland could be proposed for sustainable wastewater reclamation and optimum control of contaminats.

  3. 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.

  4. Formation of disinfection by-products in the ultraviolet/chlorine advanced oxidation process.

    Science.gov (United States)

    Wang, Ding; Bolton, James R; Andrews, Susan A; Hofmann, Ron

    2015-06-15

    Disinfection by-product (DBP) formation may be a concern when applying ultraviolet light and free chlorine (UV/chlorine) as an advanced oxidation process (AOP) for drinking water treatment, due to typically large chlorine doses (e.g. 5-10 mg L(-1) as free chlorine). A potential mitigating factor is the low chlorine contact times for this AOP treatment (e.g. seconds). Full-scale and pilot-scale test results showed minimal trihalomethane (THM) and haloacetic acid (HAA) formation during UV/chlorine treatment, while dichloroacetonitrile (DCAN) and bromochloroacetonitrile (BCAN) were produced rapidly. Adsorbable organic halide (AOX) formation was significant when applying the UV/chlorine process in water that had not been previously chlorinated, while little additional formation was observed in prechlorinated water. Chlorine photolysis led to chlorate and bromate formation, equivalent to approximately 2-17% and 0.01-0.05% of the photolyzed chlorine, respectively. No perchlorate or chlorite formation was observed. During simulated secondary disinfection of AOP-treated water, DBP formation potential for THMs, HAAs, HANs, and AOX was observed to increase approximately to the same extent as was observed for pretreatment using the more common AOP of UV combined with hydrogen peroxide (UV/H2O2).

  5. Abatement of Polychoro-1,3-butadienes in Aqueous Solution by Ozone, UV Photolysis, and Advanced Oxidation Processes (O3/H2O2 and UV/H2O2).

    Science.gov (United States)

    Lee, Minju; Merle, Tony; Rentsch, Daniel; Canonica, Silvio; von Gunten, Urs

    2017-01-03

    The abatement of 9 polychloro-1,3-butadienes (CBDs) in aqueous solution by ozone, UV-C(254 nm) photolysis, and the corresponding advanced oxidation processes (AOPs) (i.e., O3/H2O2 and UV/H2O2) was investigated. The following parameters were determined for 9 CBDs: second-order rate constants for the reactions of CBDs with ozone (kO3) (50% at specific ozone doses of 0.5 gO3/gDOC to ∼100% at ≥1.0 gO3/gDOC) were achieved for tetra-CBDs followed by (Z)-1,1,2,3,4-penta-CBD and hexa-CBD. This is consistent with the magnitude of the determined kO3 and k(•)OH. The formation of bromate, a potentially carcinogenic ozonation byproduct, could be significantly reduced by addition of H2O2. For a typical UV disinfection dose (400 J/m(2)), various extents of phototransformations (10-90%) could be achieved. However, the efficient formation of photoisomers from CBDs with E/Z configuration must be taken into account because of their potential residual toxicity. Under UV-C(254 nm) photolysis conditions, no significant effect of H2O2 addition on CBDs abatement was observed due to an efficient direct phototransformation of CBDs.

  6. 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.

  7. 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.

  8. Laser-induced removal of a dye C.I. Acid Red 87 using n-type WO3 semiconductor catalyst.

    Science.gov (United States)

    Qamar, M; Gondal, M A; Hayat, K; Yamani, Z H; Al-Hooshani, K

    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 WO3 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 (H2O2), and potassium bromate (KBrO3). 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.

  9. Rapid simultaneous analysis of 17 haloacetic acids and related halogenated water contaminants by high-performance ion chromatography-tandem mass spectrometry.

    Science.gov (United States)

    Xue, Runmiao; Donovan, Ariel; Shi, Honglan; Yang, John; Hua, Bin; Inniss, Enos; Eichholz, Todd

    2016-09-01

    Haloacetic acids (HAAs), which include chloroacetic acids, bromoacetic acids, and emerging iodoacetic acids, are toxic water disinfection byproducts. General screening methodology is lacking for simultaneously monitoring chloro-, bromo-, and iodoacetic acids. In this study, a rapid and sensitive high-performance ion chromatography-tandem mass spectrometry method for simultaneous determination of chloro-, bromo-, and iodo- acetic acids and related halogenated contaminants including bromate, bromide, iodate, and iodide was developed to directly analyze water samples after filtration, eliminating the need for preconcentration, and chemical derivatization. The resulting method was validated in both untreated and treated water matrices including tap water, bottled water, swimming pool water, and both source water and drinking water from a drinking water treatment facility to demonstrate application potential. Satisfactory accuracies and precisions were obtained for all types of tested samples. The detection limits of this newly developed method were lower or comparable with similar techniques without the need for extensive sample treatment requirement and it includes all HAAs and other halogenated compounds. This provides a powerful methodology to water facilities for routine water quality monitoring and related water research, especially for the emerging iodoacetic acids. Graphical abstract High performance ion chromatography-tandem mass spectrometry method for detection of haloacetic acids in water.

  10. 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.

  11. 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.

  12. 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.

  13. 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.

  14. Research on Spectrophotometric Determination of Nanotrace Vanadium by Catalytic Photometry%纤痕量钒的催化光度法测定研究

    Institute of Scientific and Technical Information of China (English)

    王淑志

    2011-01-01

    A new catalytic kinetic spectrotmetic method for the determination of nanotrace vanadium based on index reaction between potassium bromate and Calmagite (R)in H3PO4 medium has been established. The optimum conditions had been investigated. The calibration curves are obtained over the range 0~100pg/ml of vanadium and detection limit was 2.36 pg/ml. The apparent activation energy of this catalytic reaction was found to be 44.91kJ/mol and the apparent rate constant of this catalytic reaction was found to be 1.45×10-3 s-1. The method has been applied to determination of vanadium in water samples with satisfactory results.%在磷酸介质中,钒(V)强烈的催化溴酸钾氧化钙指示剂褪色的指示反应,研究了该催化反应的最佳实验条件,建立了测定钒的新方法.方法的测定范围是0~100pg/ml,检出限为2.36pg/ml.催化反应的表观活化能为44.91kJ/mol,表观速率常数为1.45x10 s.方法用于水样中痕量钒的测定,结果满意.

  15. Formation of oxidation byproducts from ozonation of wastewater.

    Science.gov (United States)

    Wert, Eric C; Rosario-Ortiz, Fernando L; Drury, Doug D; Snyder, Shane A

    2007-04-01

    Disinfection byproduct (DBP) formation in tertiary wastewater was examined after ozonation (O(3)) and advanced oxidation with O(3) and hydrogen peroxide (O(3)/H(2)O(2)). O(3) and O(3)/H(2)O(2) were applied at multiple dosages to investigate DBP formation during coliform disinfection and trace contaminant oxidation. Results showed O(3) provided superior disinfection of fecal and total coliforms compared to O(3)/H(2)O(2). Color, UV absorbance, and SUVA were reduced by O(3) and O(3)/H(2)O(2), offering wastewater utilities a few potential surrogates to monitor disinfection or trace contaminant oxidation. At equivalent O(3) dosages, O(3)/H(2)O(2) produced greater concentrations of assimilable organic carbon (5-52%), aldehydes (31-47%), and carboxylic acids (12-43%) compared to O(3) alone, indicating that organic DBP formation is largely dependent upon hydroxyl radical exposure. Bromate formation occurred when O(3) dosages exceeded the O(3) demand of the wastewater. Bench-scale tests with free chlorine showed O(3) is capable of reducing total organic halide (TOX) formation potential by at least 20%. In summary, O(3) provided superior disinfection compared to O(3)/H(2)O(2) while minimizing DBP concentrations. These are important considerations for water reuse, aquifer storage and recovery, and advanced wastewater treatment applications.

  16. Simultaneous Bioreduction of Multiple Oxidized Contaminants Using a Membrane Biofilm Reactor.

    Science.gov (United States)

    Li, Haixiang; Lin, Hua; Xu, Xiaoyin; Jiang, Minmin; Chang, Chein-Chi; Xia, Siqing

    2017-02-01

      This study tests a hydrogen-based membrane biofilm reactor (MBfR) to investigate simultaneous bioreduction of selected oxidized contaminants, including nitrate (-N), sulfate (), bromate (), chromate (Cr(VI)) and para-chloronitrobenzene (p-CNB). The experiments demonstrate that MBfR can achieve high performance for contaminants bioreduction to harmless or immobile forms in 240 days, with a maximum reduction fluxes of 0.901 g -N/m2·d, 1.573 g /m2·d, 0.009 g /m2·d, 0.022 g Cr(VI)/m2·d, and 0.043 g p-CNB/m2·d. Increasing H2 pressure and decreasing influent surface loading enhanced removal efficiency of the reactor. Flux analysis indicates that nitrate and sulfate reductions competed more strongly than , Cr(VI) and p-CNB reduction. The average H2 utilization rate, H2 flux, and H2 utilization efficiency of the reactor were 0.026 to 0.052 mg H2/cm3·d, 0.024 to 0.046 mg H2/cm2·d, and 97.5% to 99.3% (nearly 100%). Results show the hydrogen-based MBfR may be suitable for removing multiple oxidized contaminants in drinking water or groundwater.

  17. Poly(ethylene oxide)-bonded stationary phase for separation of inorganic anions in capillary ion chromatography.

    Science.gov (United States)

    Linda, Roza; Lim, Lee Wah; Takeuchi, Toyohide

    2013-06-14

    A tosylated-poly(ethylene oxide) (PEO) reagent was reacted with primary amino groups of an aminopropylsilica packing material (TSKgel NH2-60) in acetonitrile to form PEO-bonded stationary phase. The reaction was a single and simple step reaction. The prepared stationary phase was able to separate inorganic anions. The retention behavior of six common inorganic anions on the prepared stationary phase was examined under various eluent conditions in order to clarify its separation/retention mechanism. The elution order of the tested anions was iodate, bromate, bromide, nitrate, iodide, and thiocyanate, which was similar as observed in common ion chromatography. The retention of inorganic anions could be manipulated by ion exchange interaction which is expected that the eluent cation is coordinated among the PEO chains and it works as the anion-exchange site. Cations and anions of the eluent therefore affected the retention of sample anions. We demonstrated that the retention of the analyte anions decreased with increasing eluent concentration. The repeatability of retention time for the six anions was satisfactory on this column with relative standard deviation values from 1.1 to 4.3% when 10mM sodium chloride was used as the eluent. Compared with the unmodified TSKgel NH2-60, the prepared stationary phase retained inorganic anions more strongly and the selectivity was also improved. The present stationary phase was applied for the determination of inorganic anions contained in various water samples.

  18. 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.

  19. 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.

  20. 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.

  1. Zeolitic polyoxometalate-based metal-organic frameworks (Z-POMOFs): computational evaluation of hypothetical polymorphs and the successful targeted synthesis of the redox-active Z-POMOF1.

    Science.gov (United States)

    Rodriguez-Albelo, L Marleny; Ruiz-Salvador, A Rabdel; Sampieri, Alvaro; Lewis, Dewi W; Gómez, Ariel; Nohra, Brigitte; Mialane, Pierre; Marrot, Jérôme; Sécheresse, Francis; Mellot-Draznieks, Caroline; Ngo Biboum, Rosa; Keita, Bineta; Nadjo, Louis; Dolbecq, Anne

    2009-11-11

    The targeted design and simulation of a new family of zeolitic metal-organic frameworks (MOFs) based on benzenedicarboxylate (BDC) as the ligand and epsilon-type Keggin polyoxometalates (POMs) as building units, named here Z-POMOFs, have been performed. A key feature is the use of the analogy between the connectivity of silicon in dense minerals and zeolites with that of the epsilon-type Keggin POMs capped with Zn(II) ions. Handling the epsilon-Keggin as a building block, a selection of 21 zeotype structures, together with a series of dense minerals were constructed and their relative stabilities computed. Among these Z-POMOFs, the cristobalite-like structure was predicted to be the most stable structure. This prediction has been experimentally validated by the targeted synthesis of the first experimental Z-POMOF structure, which was strikingly found to possess the cristobalite topology, with three interpenetrated networks. Crystals of [NBu(4)](3)[PMo(V)(8)Mo(VI)(4)O(36)(OH)(4)Zn(4)(BDC)(2)].2H(2)O (Z-POMOF1) have been isolated under hydrothermal conditions from the reduction of ammonium heptamolybdate in the presence of phosphorous acid and Zn(II) ions. Tetrabutylammonium cations play the role of counterions and space-filling agents in this tridimensional interpenetrated framework. Moreover, the electrochemistry of the epsilon-Keggin POM is maintained and can be exploited in the insoluble Z-POMOF1 framework, as demonstrated by the electrocatalytic reduction of bromate.

  2. 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.

  3. Defective DNA repair and increased chromatin binding of DNA repair factors in Down syndrome fibroblasts.

    Science.gov (United States)

    Necchi, Daniela; Pinto, Antonella; Tillhon, Micol; Dutto, Ilaria; Serafini, Melania Maria; Lanni, Cristina; Govoni, Stefano; Racchi, Marco; Prosperi, Ennio

    2015-10-01

    Down syndrome (DS) is characterized by genetic instability, neurodegeneration, and premature aging. However, the molecular mechanisms leading to this phenotype are not yet well understood. Here, we report that DS fibroblasts from both fetal and adult donors show the presence of oxidative DNA base damage, such as dihydro-8-oxoguanine (8-oxodG), and activation of a DNA damage response (DDR), already during unperturbed growth conditions. DDR with checkpoint activation was indicated by histone H2AX and Chk2 protein phosphorylation, and by increased p53 protein levels. In addition, both fetal and adult DS fibroblasts were more sensitive to oxidative DNA damage induced by potassium bromate, and were defective in the removal of 8-oxodG, as compared with age-matched cells from control healthy donors. The analysis of core proteins participating in base excision repair (BER), such as XRCC1 and DNA polymerase β, showed that higher amounts of these factors were bound to chromatin in DS than in control cells, even in the absence of DNA damage. These findings occurred in concomitance with increased levels of phosphorylated XRCC1 detected in DS cells. These results indicate that DS cells exhibit a BER deficiency, which is associated with prolonged chromatin association of core BER factors.

  4. Simple and sensitive synchronous- fluorescence method for the determination of trace bisphenol S based on its inhibitory effect on the fluorescence quenching reaction of rhodamine B.

    Science.gov (United States)

    Cao, Gui-ping; Chen, Ting; Zhuang, Ya-feng

    2013-07-01

    An inhibitory kinetic fluorimetric method is reported for the determination of trace bisphenol S (BPS). The proposed method is based on the inhibitory effect of BPS on the fluorescence quenching of rhodamine B (RhB) caused by potassium bromate in a dilute phosphoric acid medium. Under the optimal conditions of the experiment, the detection limit for BPS was 0.021 mg/L, and the linear range of determination was from 0.035 mg/L to 0.750 mg/L. The relative standard deviations of 11 measurements for 0.20 mg/L and 0.40 mg/L BPS solutions were 2.74 % and 1.87 %, respectively. The method was successfully applied to the determination of bisphenol S derived from commercially available plastic film samples in hot water. A possible reaction mechanism of the inhibitory effect of BPS on the fluorescence quenching of RhB was proposed.

  5. 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.

  6. 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.

  7. [Quantification of acrylamide in foods by gas chromatography-mass spectrometry coupled with pro-column derivatization].

    Science.gov (United States)

    Yang, Sichao; Zhang, Hui; Wang, Junhan; Chen, Fang

    2011-05-01

    The quantification of acrylamide in foods was investigated by gas chromatography-mass spectrometry (GC-MS). In this method, (13)C3-acrylamide was used as an internal standard. The samples were homogenized, defatted with hexane and extracted with ethyl acetate for twice. The derivatization of acrylamide into 2-bromopropenamide (2-BPA) was done using potassium bromide/potassium bromate at 4 degrees C for 90 min. Selective ion monitoring mode was chosen to monitor objective chromatography. This method had a good linearity between 0.05-2.00 mg/kg (r2 = 0.9995), and the limits of detection and quantification were 3 microg/kg and 7 microg/kg, respectively. The recoveries of acrylamide were in the range of 62.7%-65.5%. In order to confirm this GC-MS method, the acrylamide in foods was also determined by high performance liquid chromatography coupled to quadrupole tandem mass spectrometry (HPLC-MS/MS), which had been proved in our laboratory. The concentrations of acrylamide in the samples quantified by GC-MS were slightly higher than those detected by HPLC-MS/MS. This method can be used to quantify acrylamide in normal foods.

  8. Determination of acrylamide in starch-based foods by HPLC with pre-column ultraviolet derivatization.

    Science.gov (United States)

    Geng, Zhiming; Wang, Peng; Liu, Aiming

    2011-01-01

    A new method is developed for the determination of acrylamide in starch-based foods. The method included the extraction of acrylamide with water, defatting with hexane, derivatization with potassium bromate (KBrO(3)) and potassium bromide (KBr), liquid-liquid extraction with ethyl acetate-hexane (4:1), and concentration. The final analyte (2-bromopropenamide, 2-BPA) is analyzed by high-performance liquid chromatography coupled with diode array detection for quantification and by gas chromatography coupled to mass spectrometry for confirmation. The chromatographic analysis is performed on an ODS-3 C(18) column, and good retention and peak response of acrylamide are achieved under the optimal conditions. The limit of detection and quantitation are estimated to be 15 and 50 μg/kg, respectively. The recoveries of acrylamide from the commercial samples are spiked at levels of 50-1000 μg/kg, and range between 89.6 and 102.0%. These results show that this method should be regarded as a new, low-cost, and robust alternative for conventional investigation of acrylamide.

  9. Rapid determination of acrylamide contaminant in conventional fried foods by gas chromatography with electron capture detector.

    Science.gov (United States)

    Zhang, Yu; Dong, Yi; Ren, Yiping; Zhang, Ying

    2006-05-26

    Gas chromatography coupled with electron capture detector (GC-ECD) was successfully developed and applied for the rapid determination of acrylamide in conventional fried foods, such as potato crisps, potato chips, and fried chicken wings. The method included defatting with n-hexane, extraction with aqueous solution of sodium chloride (NaCl), derivatization with potassium bromate (KBrO3) and potassium bromide (KBr), and liquid-liquid extraction with ethyl acetate. The final acrylamide extract was analyzed by GC-ECD for quantification and by GC-MS for confirmation. The chromatographic analysis was performed on the HP-INNOWax capillary column, and good retention and peak response of acrylamide were achieved under the optimal conditions (numbers of theoretical plates N = 83,815). The limit of detection (LOD) was estimated to be 0.1 microg kg(-1) on the basis of ECD technique. Recoveries of acrylamide from conventional samples spiked at levels of 150, 500 and 1000 microg kg(-1) (n = 4 for each level) ranged between 87 and 97% with relative standard deviations (RSD) of less than 4%. Furthermore, the GC-ECD method showed that no clean-up steps of acrylamide derivative would be performed prior to injection and was slightly more sensitive than the MS/MS-based methods. Validation and quantification results demonstrated that this method should be regarded as a new, low-cost, and robust alternative for conventional investigation of acrylamide.

  10. 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.

  11. Studies on the Chemical Constituents from Marine Bryozoan Cryptosula pallasiana

    Directory of Open Access Journals (Sweden)

    Xiang-Rong Tian

    2015-06-01

    Full Text Available The aim of this study was to investigate the chemical constituents of marine bryozoan Cryptosula pallasiana inhabiting Huang Island of China. Three aromatic compounds, p-methylsulfonylmethyl-phenol (1, p-hydroxybenzaldehyde (4 and methylparaben (5, nine alkaloids, 7-bromoquinolin-4(1H-one (2, 7-bromo-2,4(1H,3H-quinazolinedione (3, benzamide (6, phenylacetamide (7, 4(3H-quinazolinone (8, thymine (9, uracil (10, hypoxanthine (11 and tryptophan (12, together with two glycerol derivatives, glycerol (13 and monoheneicosanoin (14, were isolated for the first time from this marine bryozoan. Among the isolates, compounds 1 and 2 were new natural products, and their spectral traits were reported for the first time. The structures of the two compounds were elucidated by extensive spectroscopic analyses, including HR-ESI-MS, EI-MS, 1D- and 2D-NMR techniques. The isolated compounds 1–3 were evaluated for their cytotoxicity against HL-60 human myeloid leukemia cell line. The results showed that bromated alkaloid (3 appeared strong cytotoxicity against HL-60 cells with IC 50 value of 11.87 µg/mL, while compounds 1 and 2 were inactivity.

  12. A nanoliter-scale open chemical reactor.

    Science.gov (United States)

    Galas, Jean-Christophe; Haghiri-Gosnet, Anne-Marie; Estévez-Torres, André

    2013-02-01

    An open chemical reactor is a container that exchanges matter with the exterior. Well-mixed open chemical reactors, called continuous stirred tank reactors (CSTR), have been instrumental for investigating the dynamics of out-of-equilibrium chemical processes, such as oscillations, bistability, and chaos. Here, we introduce a microfluidic CSTR, called μCSTR, that reduces reagent consumption by six orders of magnitude. It consists of an annular reactor with four inlets and one outlet fabricated in PDMS using multi-layer soft lithography. A monolithic peristaltic pump feeds fresh reagents into the reactor through the inlets. After each injection the content of the reactor is continuously mixed with a second peristaltic pump. The efficiency of the μCSTR is experimentally characterized using a bromate, sulfite, ferrocyanide pH oscillator. Simulations accounting for the digital injection process are in agreement with experimental results. The low consumption of the μCSTR will be advantageous for investigating out-of-equilibrium dynamics of chemical processes involving biomolecules. These studies have been scarce so far because a miniaturized version of a CSTR was not available.

  13. 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.

  14. 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.

  15. A model for imperfect mixing in a CSTR

    Science.gov (United States)

    Bar-Eli, Kedma; Noyes, Richard M.

    1986-09-01

    When a chemical reaction is carried out in a continuously stirred tank reactor, the behavior may be significantly affected by the efficiency with which the entering chemicals are mixed with the main contents of the reactor. We have developed a model for this effect which assumes that a feed of premixed chemicals remains for a while in totally segregated packets before they are rapidly and perfectly mixed with the rest of the system. The time of this initial segregation is affected by the efficiency of stirring in the reactor. The model has been tested by computations on a mechanism developed by Roelofs et al. for a reaction which would oscillate even in a closed system. It has also been tested by computations on the rapid autocatalytic oxidation of cerous ion by bromate in the presence of a small amount of bromide. The results are qualitatively consistent with effects observed experimentally and in computations with other models including a somewhat similar one by Kumpinsky and Epstein. More quantitative tests should recognize the difference whether two streams of chemicals enter the reactor independently or are premixed before they do so.

  16. Determination of caffeine using oscillating chemical reaction in a CSTR.

    Science.gov (United States)

    Gao, Jinzhang; Ren, Jie; Yang, Wu; Liu, XiuHui; Yang, Hua

    2003-07-14

    A new analytical method for the determination of caffeine by the sequential perturbation caused by different amounts of caffeine on the oscillating chemical system involving the manganese(II)-catalyzed reaction between potassium bromate and tyrosine in acidic medium in a CSTR was proposed. The method exposed for the first time in this work. It relies on the relationship between the changes in the oscillation amplitude of the chemical system and the concentration of caffeine. The calibration curve fits a second-order polynomial equation very well when the concentration of caffeine over the range 4.0 x 10(-6) - 1.2 x 10(-4) M (r = 0.9968). The effect of influential variables, such as the concentration of reaction components, injection point, temperature, flow rate and stirring rate were studied. Some aspects of the potential mechanism of action of caffeine on the chemical oscillating system were also discussed. A real sample was determined and the result was satisfactory.

  17. 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.

  18. 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.

  19. Preparation and characterization of poly(acrylic acid)-hydroxyethyl cellulose graft copolymer.

    Science.gov (United States)

    Abdel-Halim, E S

    2012-10-01

    Poly(acrylic acid) hydroxyethyl cellulose [poly(AA)-HEC] graft copolymer was prepared by polymerizing acrylic acid (AA) with hydroxyethyl cellulose (HEC) using potassium bromate/thiourea dioxide (KBrO(3)/TUD) as redox initiation system. The polymerization reaction was carried out under a variety of conditions including concentrations of AA, KBrO(3) and TUD, material to liquor ratio and polymerization temperature. The polymerization reaction was monitored by withdrawing samples from the reaction medium and measuring the total conversion. The rheological properties of the poly(AA)-HEC graft copolymer were investigated. The total conversion and rheological properties of the graft copolymer depended on the ratio of KBrO(3) to TUD and on acrylic acid concentration as well as temperature and material to liquor ratio. Optimum conditions of the graft copolymer preparation were 30 mmol KBrO(3) and 30 mmol TUD/100g HEC, 100% AA (based on weight of HEC), duration 2h at temperature 50 °C using a material to liquor ratio of 1:10.

  20. Belousov-Zhabotinsky autonomic hydrogel composites: Regulating waves via asymmetry

    Science.gov (United States)

    Buskohl, Philip R.; Vaia, Richard A.

    2016-01-01

    Belousov-Zhabotinsky (BZ) autonomic hydrogel composites contain active nodes of immobilized catalyst (Ru) encased within a nonactive matrix. Designing functional hierarchies of chemical and mechanical communication between these nodes enables applications ranging from encryption, sensors, and mechanochemical actuators to artificial skin. However, robust design rules and verification of computational models are challenged by insufficient understanding of the relative importance of local (molecular) heterogeneities, active node shape, and embedment geometry on transient and steady-state behavior. We demonstrate the predominance of asymmetric embedment and node shape in low-strain, BZ-gelatin composites and correlate behavior with gradients in BZ reactants. Asymmetric embedment of square and rectangular nodes results in directional steady-state waves that initiate at the embedded edge and propagate toward the free edge. In contrast, symmetric embedment does not produce preferential wave propagation because of a lack of diffusion gradient across the catalyzed region. The initiation at the embedded edge is correlated with bromide absorption by the inactive matrix, which locally elevates the bromate concentration required for catalyst oxidation. The competition between embedment asymmetry and node geometry was used to demonstrate a repeatable switch in wave direction that functions as a signal delay. Furthermore, signal propagation in or out of the composite was demonstrated via embedment asymmetry and relative dimensions of a T-shaped active network node. Overall, structural asymmetry provides a robust approach to controlling initiation and orientation of chemical-mechanical communication within composite BZ gels. PMID:27679818

  1. Study on Pentosan from Corn Fiber by Alkaline Peroxide Extraction and Oxidative Cross-linking Property of Pentosan%碱性过氧化氢法提取玉米皮戊聚糖及其氧化交联性质的研究

    Institute of Scientific and Technical Information of China (English)

    王文侠; 张晓静; 宋春丽; 李建强

    2012-01-01

    Extracting pentosan was studied by alkaline peroxide treatment of the corn fiber. Extracted pentosan with ammomium persulfae, potassium bromate and hydrogen peroxide/peroxidase was studied. The effects of the concentration of hydrogen peroxide, pH, ratio of solid to liquid, temperature, extraction time and temperature on the yield of pentosan were studied respectively. Based on the results, other four key factors except ratio of solid to liquid were optimized through response surface methodology with four factors and three levels based on the principle of Box-Behnken design. The results showed that the optimum extraction conditions were 85 ℃, hydrogen peroxide concentration 2.14%, pH 11.65, 2.23 h, ratio of substrate and water 1:25(m/V). Under this optimal conditions, the yield of pentosan was highly reach to 47.18%. Extracted pentosan with ammomium persulfae, potassium bromate and hydrogen peroxide/peroxidase gave a slow increase in viscosity and when pentosan concentration was 1%(m/V), optimum concentration of three oxidant was 0.75%, 0.17%, 10 U/g pentosan respectively.%以玉米皮为原料,对碱性过氧化氢提取玉米皮中的戊聚糖提取条件以及戊聚糖的氧化交联性质进行研究.在考察H2O2溶液的体积分数、H2O2的pH值、固液比、提取时间、提取温度5个因素对戊聚糖得率影响的基础上,根据Box-Benhnken中心组合试验设计原理,采用四因素三水平响应面分析法,确定戊聚糖提取的最优条件是:固液比为1∶25(m/V),H2O2溶液体积分数2.14%,pH 11.65,提取温度85℃,提取时间2.23 h,此条件下戊聚糖得率达到47.18%.戊聚糖的氧化交联性与氧化剂的用量有关,用量过多或过少均会使氧化交联程度减弱.在糖质量分数为1%时,(NH4)2S2O8、KBrO3及过氧化氢与过氧化物酶(H2O2/POX)3个体系中氧化剂的最适用量分别为0.75%,0.17%,10U/g戊聚糖,此时有利于戊聚糖氧化凝胶的形成.

  2. 天津开发区净水厂三期工程紫外线消毒系统应用研究%Application study on UV disinfection system in the third stage project of Tianjin development zone Water Treatment Plant

    Institute of Scientific and Technical Information of China (English)

    聂雪彪; 刘文君; 何凤华

    2011-01-01

    The UV - chlorine disinfection process was employed in the third stage project in Tianjin development zone water treatment plant. The production water and pipe - network water were tested, and the results showed: Cryptozoite, Giardia, coronavirus and adenovirus were not found; the coliform, total plate count, HPC (Heterotrophic bacteria count), bromate, haloacetic acids, and trihalomethanes in production water and pipe-network water all met the standards; when UVT (UV transmittance) in UV disinfection reactor was relatively high (UVT=95%), the power of UV disinfection equipment could be lowered; there was still some space for the decrease of chlorine dosage in the UV-chlorine disinfection process.%天津开发区净水厂三期工程采用紫外线联合氯消毒工艺,对主要工艺出水及管网水进行检测,未检出隐孢子虫、贾第鞭毛虫、冠状病毒和腺病毒;出厂水及管网水中总大肠菌群、菌落总数、HPC(Heterotrophic bacteria count,异养菌计数),以及溴酸盐、卤乙酸、三卤甲烷等理化指标均达到相关标准要求;紫外线反应器进水UVT(UV transmittance,紫外透光率)较高时(如UVT=95%),可降低紫外线消毒设备功率;联合消毒的加氯量经初步探究有一定的降低空间.

  3. Determination of trace uranium by resonance fluorescence method coupled with photo-catalytic technology and dual cloud point extraction.

    Science.gov (United States)

    Li, Jiekang; Li, Guirong; Han, Qian

    2016-12-01

    In this paper, two kinds of salophens (Sal) with different solubilities, Sal1 and Sal2, have been respectively synthesized, and they all can combine with uranyl to form stable complexes: [UO2(2+)-Sal1] and [UO2(2+)-Sal2]. Among them, [UO2(2+)-Sal1] was used as ligand to extract uranium in complex samples by dual cloud point extraction (dCPE), and [UO2(2+)-Sal2] was used as catalyst for the determination of uranium by photocatalytic resonance fluorescence (RF) method. The photocatalytic characteristic of [UO2(2+)-Sal2] on the oxidized pyronine Y (PRY) by potassium bromate which leads to the decrease of RF intensity of PRY were studied. The reduced value of RF intensity of reaction system (ΔF) is in proportional to the concentration of uranium (c), and a novel photo-catalytic RF method was developed for the determination of trace uranium (VI) after dCPE. The combination of photo-catalytic RF techniques and dCPE procedure endows the presented methods with enhanced sensitivity and selectivity. Under optimal conditions, the linear calibration curves range for 0.067 to 6.57ngmL(-1), the linear regression equation was ΔF=438.0 c (ngmL(-1))+175.6 with the correlation coefficient r=0.9981. The limit of detection was 0.066ngmL(-1). The proposed method was successfully applied for the separation and determination of uranium in real samples with the recoveries of 95.0-103.5%. The mechanisms of the indicator reaction and dCPE are discussed.

  4. 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.

  5. 溴酸钾光催化降解刚果红的研究

    Institute of Scientific and Technical Information of China (English)

    毛晓明; 靳永胜

    2014-01-01

    An experiment demonstrated that the dye of Congo Red (CR) in water could be photocatalytic degraded effectively in the presence of potassium bromate (KBrO 3) under simulated sunlight irradiation. The degradation efficiency of CR increased as the dosage of KBrO 3 increased, while decreased as the CR initial concentration increased. When the dosage of KBrO 3 was 1.5 g·L-1, the degradation of CR was up to 100%in 30 min. This paper revealed that the degradation reaction followed pseudo first-order kinetics. The apparent activation energy (Ea) for 40 mg·L-1 CR between 298 K and 328 K was 8.073 kJ·mol-1. The lower Ea indicated that the breakdown of the chemical bonds of CR in photodegradation reaction required less energy. By examining the effect of isopropanol (IPA), ethanol (EA) and methanol (MT) as the scavenger of hydroxyl radicals, it was shown that hydroxyl radicals played a main role in photodegradation of CR with KBrO 3.%本文研究表明溴酸钾(KBrO3)可光催化降解刚果红,刚果红的降解效率随溴酸钾用量的增加而增加,随刚果红初始浓度的增加而降低。较低的活化能表明较少的能量即可使刚果红的化学键断裂。捕获剂实验结果表明羟基自由基在刚果红的光催化降解反应中起主要作用。

  6. 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.

  7. Simultaneous removal of selected oxidized contaminants in groundwater using a continuously stirred hydrogen-based membrane biofilm reactor

    Institute of Scientific and Technical Information of China (English)

    Siqing Xia; Jun Liang; Xiaoyin Xu; Shuang Shen

    2013-01-01

    A laboratory trial was conducted for evaluating the capability of a continuously stirred hydrogen-based membrane biofilm reactor to simultaneously reduce nitrate (NO3--N),sulfate (SO42-),bromate (BrO3-),hexavalent chromium (Cr(Ⅵ)) and parachloronitrobenzene (p-CNB).The reactor contained two bundles of hollow fiber membranes functioning as an autotrophic biofilm carrier and hydrogen pipe as well.On the condition that hydrogen was supplied as electron donor and diffused into water through membrane pores,autohydrogenotrophic bacteria were capable of reducing contaminants to forms with lower toxicity.Reduction occurred within 1 day and removal fluxes for NO3--N,SO42-,BrO3-,Cr(Ⅵ),and p-CNB reached 0.641,2.396,0.008,0.016 and 0.031 g/(day.m2),respectively after 112 days of continuous operation.Except for the fact that sulfate was 37% removed under high surface loading,the other four contaminants were reduced by over 95%.The removal flux comparison between phases varying in surface loading and H2 pressure showed that decreasing surface loading or increasing H2 pressure would promote removal flux.Competition for electrons occurred among the five contaminants.Electron-equivalent flux analysis showed that the amount of utilized hydrogen was mainly controlled by NO2--N and SO42-reduction,which accounted for over 99% of the electron flux altogether.It also indicated the electron acceptor order,showing that nitrate was the most prior electron acceptor while sulfate was the second of the five contaminants.

  8. Cellular distribution of cell cycle-related molecules in the renal tubules of rats treated with renal carcinogens for 28 days: relationship between cell cycle aberration and carcinogenesis.

    Science.gov (United States)

    Taniai, Eriko; Hayashi, Hitomi; Yafune, Atsunori; Watanabe, Maiko; Akane, Hirotoshi; Suzuki, Kazuhiko; Mitsumori, Kunitoshi; Shibutani, Makoto

    2012-09-01

    Some renal carcinogens can induce karyomegaly, which reflects aberrant cell division in the renal tubules, from the early stages of exposure. To clarify the cell cycle-related changes during the early stages of renal carcinogenesis, we performed immunohistochemical analysis of tubular cells in male F344 rats treated with carcinogenic doses of representative renal carcinogens for 28 days. For this purpose, the karyomegaly-inducing carcinogens ochratoxin A (OTA), ferric nitrilotriacetic acid, and monuron, and the non-karyomegaly-inducing carcinogens tris(2-chloroethyl) phosphate and potassium bromate were examined. For comparison, a karyomegaly-inducing non-carcinogen, p-nitrobenzoic acid, and a non-carcinogenic non-karyomegaly-inducing renal toxicant, acetaminophen, were also examined. The outer stripe of the outer medulla (OSOM) and the cortex + OSOM were subjected to morphometric analysis of immunoreactive proximal tubular cells. Renal carcinogens, irrespective of their karyomegaly-inducing potential, increased proximal tubular cell proliferation accompanied by an increase in topoisomerase IIα-immunoreactive cells, suggesting a reflection of cell proliferation. Karyomegaly-inducing carcinogens increased nuclear Cdc2-, γH2AX-, and phosphorylated Chk2-immunoreactive cells in both areas, the former two acting in response to DNA damage and the latter one suggestive of sustained G₂. OTA, an OSOM-targeting carcinogen, could easily be distinguished from untreated controls and non-carcinogens by evaluation of molecules responding to DNA damage and G₂/M transition in the OSOM. Thus, all renal carcinogens examined facilitated proximal tubular proliferation by repeated short-term treatment. Among these, karyomegaly-inducing carcinogens may cause DNA damage and G₂ arrest in the target tubular cells.

  9. A novel copper(II) complex constructed with mixed ligands of biphenyl-4,4'-dicarboxylic acid (H 2bpdc) and dipyrido[3,2-d:2',3'-f]quinoxaline (Dpq): Synthesis, structure, electrochemistry and electrocatalysis

    Science.gov (United States)

    Lin, HongYan; Wang, XiuLi; Hu, HaiLiang; Chen, BaoKuan; Liu, GuoCheng

    2009-03-01

    A novel metal-organic framework [Cu 2(bpdc) 2(Dpq) 2(H 2O)]·H 2O ( 1) has been obtained from hydrothermal reaction of copper chloride with the mixed ligands [biphenyl-4,4'-dicarboxylic acid (H 2bpdc) and dipyrido[3,2-d:2',3'-f]quinoxaline (Dpq)], and structurally characterized by elemental analysis, IR, TG and single-crystal X-ray diffraction analysis. The unique feature is that there simultaneously exist two kinds of one-dimensional (1-D) zigzag polymeric chains in complex 1. Moreover, the 1-D polymeric chains are ultimately packed into a three-dimensional (3-D) supramolecular framework through two different hydrogen bonding interactions. The adjacent different chains are linked by C-H⋯O hydrogen bonding interactions, and the same kind chains are further connected through C-H⋯π stacking interactions. Additionally, the complex 1 was used as solid bulk-modifier to fabricate renewable carbon paste electrode (Cu-CPE) by the direct mixing method. The electrochemical behavior and electrocatalysis of Cu-CPE have been studied in detail. The results indicate that Cu-CPE give one-electron quasi-reversible redox waves in potential range of 400 to -300 mV due to the metal copper ion Cu(II)/Cu(I). The Cu-CPE showed good electrocatalytic activity toward the reduction of the bromate, nitrite and hydrogen peroxide. The electrocatalytic reduction peak currents of KBrO 3, KNO 2 and H 2O 2 showed a linear dependence on their concentrations. All of the results revealed that the Cu-CPE had a good reproducibility, remarkable long-term stability and especially good surface renewability by simple mechanical polishing in the event of surface fouling, which is important for practical application.

  10. UV/H2O2联用工艺去除水中微量有机污染物的中试研究%Pilot study of UV/H2O2 combined process on removing micro organic pollutants in water

    Institute of Scientific and Technical Information of China (English)

    夏萍; 叶辉; 周新宇; 张东; 王铮

    2012-01-01

    为了考察UV/H2O2工艺对微量有机物的去除效果,在砂滤池出水后接UV/H2O2高级氧化中试设备,并投加了特征污染物(阿特拉津、臭味物质2-MIB与Geosmine).结果表明,UV/H2O2工艺对Geosmine去除效果最好,去除率能达到90%以上,对MIB和阿特拉津的去除效果比较接近,去除率均在50%以上,对UV254的去除率为20%~38%.在UV/H2O2工艺中无溴酸盐生成.%To study the removal efficiency of UV/H2O2 process on micro organic pollutants, UV/H2O2 pilot equipment was used to treat the sedimentation effluent dosed with target pollutants (including Atrazine, odor matter 2 - MIB, and Geosmine). The results showed: UV/H2O2 had the best efficiency on removing Geosmine with the removal rate over 90%. The removal effect of MIB and Atrazine was alike, and the removal rates both reached over 50%. The removal rate of UV254 was 20%-38%. No bromate was formed in the UV/H2O2 process.

  11. Gaseous, chlorine-free chlorine dioxide for drinking water

    Energy Technology Data Exchange (ETDEWEB)

    Gordon, G. [Miami Univ., Oxford, OH (United States); Rosenblatt, A. [CDG Technology Inc., New York, NY (United States)

    1996-11-01

    The benefits of applying chlorine dioxide (ClO{sub 2}) for the oxidative treatment of drinking water are well established. Chlorine dioxide treated finished water typically has substantially lower trihalomethane (THM) levels because ClO{sub 2} will not form chlorinated organic species as a by-product of disinfection. The THMs that are formed are probably due to chlorine from the generator or chlorine used to maintain a post-disinfection residual. An emerging regulatory issue concerning the formation of disinfection by-products (DBPs) is causing the water industry to set standards for the generation and delivery of ClO{sub 2}. The Federal Register (11 February 1994) contains language developed to limit the production of the unwanted inorganic by-products chlorite (ClO{sub 2}{sup -}), chlorate (ClO{sub 3}{sup -}), and bromate (BrO{sub 3}{sup -}) ions by requiring utilities to maintain high (95%) generation efficiencies and by limiting the amount of excess Cl{sub 2} that can be used during the generation process. The efficiency and excess Cl{sub 2} regulations may be problematic for utilities that over-chlorinate to attain chlorine dioxide high yields. Many utilities will have to decide either to reduce the amount of Cl{sub 2} used to react with sodium chlorite (NaClO{sub 2}), thereby increasing the ClO{sub 2}{sup -} residual in finished water, or over-chlorinate to increase yields and surpass the excess Cl{sub 2} limits.

  12. 表面活性剂增敏光度法测定电镀废水中的铬(Ⅵ)%Determination of chromium (Ⅵ) in eIectropIating wastewater by surfactant sensibization spectrophotometric method

    Institute of Scientific and Technical Information of China (English)

    张梦颖; 贾华丽; 王春杰; 赵辉

    2016-01-01

    A new method for the determination of trace Cr (Ⅵ) has been developed,based on catalytic effect of chromium (Ⅵ) on the oxidative decoloration reaction of malachite green oxidized with potassium bromate ,and cetyl trimethyl ammonium bromide(CTMAB) as sensitizer in sulfuric acid medium. The factors affecting decoration reac-tion are studied. Under optimized experimental conditions ,the linear range of the determination is 0-60 μg/L for chromium (Ⅵ),and the detection limit 7.5 ×10-4μg/L. The method is successfully applied to the determination of chromium(Ⅵ) in electroplating wastewater,its relative standard deviation(n=6) is 2.1%. The results are consistent with those obtained by atomic absorption spectrometry.%在硫酸介质中以及在十六烷基三甲基溴化铵(CTMAB)存在条件下,对痕量Cr(Ⅵ)催化溴酸钾氧化孔雀石绿褪色的反应进行了研究,建立了测定痕量Cr(Ⅵ)的新方法,研究了影响褪色反应的因素。在优化实验条件下,方法的线性范围0~60μg/L,检出限为7.5×10-4μg/L。该法用于测定电镀废水中的铬(Ⅵ),相对标准偏差(n=6)为2.1%,结果与原子吸收法相符。

  13. Differential mobility spectrometry with nanospray ion source as a compact detector for small organics and inorganics.

    Science.gov (United States)

    Coy, Stephen L; Krylov, Evgeny V; Nazarov, Erkinjon G; Fornace, Albert J; Kidd, Richard D

    2013-09-01

    Electrospray ionization (ESI) is an important tool in chemical and biochemical survey and targeted analysis in many applications. For chemical detection and identification electrospray is usually used with mass spectrometry (MS). However, for screening and monitoring of chemicals of interest in light, low power field-deployable instrumentation, an alternative detection technology with chemical selectivity would be highly useful, especially since small, lightweight, chip-based gas and liquid chromatographic technologies are being developed. Our initial list of applications requiring portable instruments includes chemical surveys on Mars, medical diagnostics based on metabolites in biological samples, and water quality analysis. In this report, we evaluate ESI-Differential Mobility Spectrometry (DMS) as a compact, low-power alternative to MS detection. Use of DMS for chemically-selective detection of ESI suffers in comparison with mass spectrometry because portable MS peak capacity is greater than that of DMS by 10X or more, but the development of light, fast chip chromatography offers compensating resolution. Standalone DMS provides the chemical selectivity familiar from DMS-MS publications, and exploits the sensitivity of ion detection. We find that sub-microliter-per-minute flows and a correctly-designed interface prepare a desolvated ion stream that enables DMS to act as an effective ion filter. Results for a several small organic biomarkers and metabolites, including citric acid, azelaic acid, n-hexanoylglycine, thymidine, and caffeine, as well as compounds such as dinitrotoluene and others, have been characterized and demonstrate selective detection. Water-quality-related halogen-containing anions, fluoride through bromate, contained in liquid samples are also isolated by DMS. A reaction-chamber interface is highlighted as most practical for portable ESI-DMS instrumentation.

  14. 溴化蓖麻油多元醇合成及其制备的阻燃聚氨酯硬泡性能%The Synthesis of Bromine-containing Castor Oil Polyol and the Flame-retardant Polyurethane Foam Prooerties

    Institute of Scientific and Technical Information of China (English)

    何明; 罗振扬; 史以俊; 顾晓利; 张银萍

    2011-01-01

    A novel bromine-containing castor oil based polyol was prepared via the reaction of glycerin-exchanged castor oil and bromine.Structure of bromation product was analyzed by FT-IR.The basic characters of the polyol, such as viscosity, hydroxyl value and acid value were investigated.The effects of bromine-containing castor oil based polyols on properties of the rigid polyurethane foams, especially on their resistance to combustion, were studied by foam experiment, oxygen index, smoke density and horizontal burning experiments.It was compared with the foam prepared by RB-79 of Albemarle Corporation.It was found that the bromine-containing castor oil based polyols were effective for improving the resistance to combustion of rigid polyurethane foams, having the same effects with the commercial flame retardant RB-79 of Albemarle Corporation.%采用可再生的醇解蓖麻油多元醇为原料,与液溴进行加成反应制备溴化蓖麻油多元醇,通过红外光谱证实发生了溴化反应,并测定了产物粘度、羟值、酸值.通过发泡实验和氧指数、烟密度、水平燃烧等测试手段,考察了溴化蓖麻油基聚氨酯硬泡发泡参数和阻燃性质,并与工业级阻燃荆雅保RB-79制备的聚氨酯硬泡进行比较.结果表明,由溴化蓖麻油多元醇制备的泡沫体现出较好阻燃性能,与RB-79的阻燃效果相当.

  15. Determination of trace uranium by resonance fluorescence method coupled with photo-catalytic technology and dual cloud point extraction

    Science.gov (United States)

    Li, Jiekang; Li, Guirong; Han, Qian

    2016-12-01

    In this paper, two kinds of salophens (Sal) with different solubilities, Sal1 and Sal2, have been respectively synthesized, and they all can combine with uranyl to form stable complexes: [UO22 +-Sal1] and [UO22 +-Sal2]. Among them, [UO22 +-Sal1] was used as ligand to extract uranium in complex samples by dual cloud point extraction (dCPE), and [UO22 +-Sal2] was used as catalyst for the determination of uranium by photocatalytic resonance fluorescence (RF) method. The photocatalytic characteristic of [UO22 +-Sal2] on the oxidized pyronine Y (PRY) by potassium bromate which leads to the decrease of RF intensity of PRY were studied. The reduced value of RF intensity of reaction system (ΔF) is in proportional to the concentration of uranium (c), and a novel photo-catalytic RF method was developed for the determination of trace uranium (VI) after dCPE. The combination of photo-catalytic RF techniques and dCPE procedure endows the presented methods with enhanced sensitivity and selectivity. Under optimal conditions, the linear calibration curves range for 0.067 to 6.57 ng mL- 1, the linear regression equation was ΔF = 438.0 c (ng mL- 1) + 175.6 with the correlation coefficient r = 0.9981. The limit of detection was 0.066 ng mL- 1. The proposed method was successfully applied for the separation and determination of uranium in real samples with the recoveries of 95.0-103.5%. The mechanisms of the indicator reaction and dCPE are discussed.

  16. 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.

  17. Visible light-induced formation of corrole-manganese(V)-oxo complexes: Observation of multiple oxidation pathways.

    Science.gov (United States)

    Ka, Wai Kwong; Ngo, Fung Lee; Ranburger, Davis; Malone, Jonathan; Zhang, Rui

    2016-10-01

    Two manganese(V)-oxo corroles [Mn(V)(Cor)O] that differ in their electronic environments were produced by visible light irradiation of highly photo-labile corrole-manganese(IV) bromates. The corrole ligands under study include 5,10,15-tris(pentafluorophenyl)corrole (TPFC), and 5,10,15-triphenylcorrole (TPC). The kinetics of oxygen transfer atom (OAT) reactions with various organic reductants by these photo-generated Mn(V)(Cor)O were also studied in CH3CN and CH2Cl2 solutions. Mn(V)(Cor)O exhibits remarkable solvent and ligand effect on its reactivity and spectral behavior. In the more electron-deficient TPFC system and in the polar solvent CH3CN, Mn(V)(Cor)O returned Mn(III) corrole in the end of oxidation reactions. However, in the less polar solvent CH2Cl2 or in the less electron-deficient TPC system, Mn(IV) product was formed instead of Mn(III). Furthermore, with the same substrates and in the same solvent, the order of reactivity of Mn(V)(Cor)O was TPC>TPFC, which is inverted from that expected based on the electron-demand of corrole ligands. Our spectral and kinetic results in this study provide compelling evidence in favor of multiple oxidation pathways, where Mn(V)(Cor)O may serve as direct two-electron oxidant or undergo a disproportionation reaction to form a manganese(VI)-oxo corrole as the true oxidant. The choice of pathways is strongly dependent on the nature of the solvent and the corrole ligand.

  18. Fabrication of CdS/CdTe solar cells with transparent p-type conductive BaCuSeF back contact

    Science.gov (United States)

    Yamamoto, Koichi; Sakakima, Hiroshi; Ogawa, Yohei; Hosono, Aikyo; Okamoto, Tamotsu; Wada, Takahiro

    2015-08-01

    BaCuSeF films were applied to CdS/CdTe solar cells as back electrodes. The interfaces between the CdTe and BaCuSeF layers in the CdS/CdTe solar cells with BaCuSeF back contact deposited at substrate temperatures (TS) of 200 and 300 °C were analyzed by transmission electron microscopy (TEM) and energy dispersive X-ray spectroscopy (EDS). We clearly observed many dislocations in the CdTe layer in the CdS/CdTe solar cell with the BaCuSeF layer deposited at TS = 300 °C. We also observed a reaction layer of Cu2.72Te2 between the BaCuSeF and CdTe layers in both solar cells. We concluded that (1) the substrate temperature for the pulsed laser deposition of the BaCuSeF layer and (2) the interface between the CdTe and BaCuSeF layers are important factors for the performance of the CdTe solar cells. We obtained high conversion efficiency of 8.31% for a solar cell with a BaCuSeF layer deposited at TS = 200 °C on a CdTe surface etched in a NH3 aqueous solution. The highest conversion efficiency of 9.91% was obtained for a solar cell with a CdTe surface etched in a bromide-bromate solution.

  19. Synthesis of Piceatannol%白皮杉醇的合成

    Institute of Scientific and Technical Information of China (English)

    李晓霞; 晏日安; 段翰英

    2011-01-01

    以3,4-二甲氧基苄醇为原料,通过溴代、Arbuzov重排反应、Wittig-Homer反应和脱甲基化反应得到目标产物(E)-3,3',4,5'-四羟基二苯乙烯,即白皮杉醇.该文考察了溴代试剂、Arbuzov重排反应温度、Wittig-Horner反应中溶剂及脱甲基反应试剂等各因素对产物产率的影响,得到最佳反应条件为:以三溴化磷为溴代试剂,Arbuzov重排反应条件为100℃反应1 h,再于120~130℃反应3~4 h,以DMF为Wittig-Horner反应溶剂,无水AlCl3作为脱甲基化试剂.通过IR、1HNMR及13CNMR确定了目标产物的结构.%Starting from the 3,4-dimethoxybenzyl alcohol, 3,3', 4,5'-tetrahydroxystilbene ( piceatannol ) was synthesized through bromation, Arbuzov rearrangement followed by Wittig-Horner reaction and demethylation reaction.The effects of brominating agents, the temperature of Arbuzov rearrangement,solvent in Wittig-Horner reaction, and demethylation agents were investigated.The optimal conditions were: phosphorus tribromide being used as the brominating agent, Arbuzov rearrangement conditions of 100 ℃ for 1 h and then 120 ~ 130 ℃ for 3 ~4 h,dimethylformamide being used as the solvent in Wittig-Horner reaction, dry aluminum chloride being used as the demethylation agent.The structure of the target molecules was confirmed by means of IR, 1HNMR and 13 CNMR spectra.

  20. Trade-offs in disinfection byproduct formation associated with precursor preoxidation for control of N-nitrosodimethylamine formation.

    Science.gov (United States)

    Shah, Amisha D; Krasner, Stuart W; Lee, Chih Fen Tiffany; von Gunten, Urs; Mitch, William A

    2012-05-01

    Chloramines in drinking water may form N-nitrosodimethylamine (NDMA). Various primary disinfectants can deactivate NDMA precursors prior to chloramination. However, they promote the formation of other byproducts. This study compared the reduction in NDMA formation due to chlorine, ozone, chlorine dioxide, and UV over oxidant exposures relevant to Giardia control coupled with postchloramination under conditions relevant to drinking water practice. Ten waters impacted by treated wastewater, poly(diallyldimethylammonium chloride) (polyDADMAC) polymer, or anion exchange resin were examined. Ozone reduced NDMA formation by 50% at exposures as low as 0.4 mg×min/L. A similar reduction in NDMA formation by chlorination required ∼60 mg×min/L exposure. However, for some waters, chlorination actually increased NDMA formation at lower exposures. Chlorine dioxide typically had limited efficacy regarding NDMA precursor destruction; moreover, it increased NDMA formation in some cases. UV decreased NDMA formation by ∼30% at fluences >500 mJ/cm(2), levels relevant to advanced oxidation. For the selected pretreatment oxidant exposures, concentrations of regulated trihalomethanes, haloacetic acids, bromate, and chlorite typically remained below current regulatory levels. Chloropicrin and trichloroacetaldehyde formation were increased by preozonation or medium pressure UV followed by postchloramination. Among preoxidants, ozone achieved the greatest reduction in NDMA formation at the lowest oxidant exposure associated with each disinfectant. Accordingly, preozonation may inhibit NDMA formation with minimal risk of promotion of other byproducts. Bromide >500 μg/L generally increased NDMA formation during chloramination. Higher temperatures increased NDMA precursor destruction by preoxidants but also increased NDMA formation during postchloramination. The net effect of these opposing trends on NDMA formation was water-specific.

  1. 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.

  2. 3,5-二溴-2-氨基吡嗪的合成研究%Synthesis of 3,5-dibromopyrazin-2-amine

    Institute of Scientific and Technical Information of China (English)

    姜卫东; 王瑜; 刘明星

    2016-01-01

    The 3 ,5-dibromopyrazin-2-amine was prepared and preparation parameters were optimized. The 2-Amino pyrazine was prepared by one-pot method via rearrangement and hydrolysis reaction using 2-cyanopyrazine. 3 ,5-dibromopyrazin-2-amine was synthesized using NBS as a bromating agent. The 3 , 5-dibromopyrazin-2-amine was identified by 1 H-NMR and MS. Meanwhile, the above preparation parameters were optimized. The total yield was 62%and the purity was more than 99% (HPLC). This method has some advantages of cheap materials, simple operation, lower environment pollution, a gentle reaction conditions and higher application value for the industrial production.%制备3,5-二溴-2-氨基吡嗪,并优化工艺。以2-氰基吡嗪为原料,经水解、重排一锅法得到2-氨基吡嗪,再用N-溴代丁二酰亚胺(NBS)溴化得3,5-二溴-2-氨基吡嗪。目标产物经1H-NMR和MS确认,与标准图谱相符;改进后的制备工艺所用原料和试剂工业上易得,价格低廉,操作简单,反应温和,产品纯度高,环境污染小,总收率达到62%,含量大于99%( HPLC),可适合规模化生产。

  3. 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.

  4. 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.

    Science.gov (United States)

    Zhang, Yu; Ren, Yiping; Zhao, Hangmei; Zhang, Ying

    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 microg kg(-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 microg kg(-1) for acrylamide. The GC-MECD method achieved quantification limits of 10 microg kg(-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 microg kg(-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.

  5. Determination of Vanadium by New Catalytic Polarographic Method%催化动力学极谱法测定痕量钒

    Institute of Scientific and Technical Information of China (English)

    王术皓; 杜凌云; 张爱梅; 张美芹

    2001-01-01

    在硫酸介质中,以酒石酸为活化剂,痕量钒对溴酸钾氧化甲基橙的反应有极强的催化作用,以极谱法监测催化反应过程中甲基橙及其氧化产物浓度的变化,建立了双峰指示催化动力学极谱法测定痕量钒的新方法。方法的线性范围为0.23~3.70μg/L,检出限为0.17μg/L。方法已用于食品及水样中痕量钒的测定。%A new catalytic polarographic method for determination of traceamounts of vanadium(Ⅴ) was proposed .The method was based on the catalytic effects of V(Ⅴ) on the oxidation of methy1 orange by bromate in sulfuric acid medium with tartaric acid as an activator. The reaction was monitored by measuring the decrease of the peak height at -0.62V or the increase of the peak height at -0.52V. The linear range is 0.23~3.70 μg/L for vanadium(Ⅴ), with detection limit of 0.17 μg/L. The method was used to determine trace vanadium in food and water samples with satisfactory results.

  6. 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.

  7. DRINKING WATER DISINFECTION BYPRODUCTS:CHEMICAL CHARACTERIZATION AND TOXICITY%饮用水消毒副产物:化学特征与毒性

    Institute of Scientific and Technical Information of China (English)

    赵玉丽; 李杏放

    2011-01-01

    Disinfection of drinking water is essential to and effective for the prevention of water-borne diseases.While achieving deactivation of microbial pathogens to minimize the acute risk, an unintentional consequence is the formation of disinfection byproducts (DBPs) resulting from reactions of disinfectants with natural organic materials (NOMs) in water. Epidemiological studies show potential associations of increased risk of bladder cancer and adverse health effects with DBPs. Balancing microbial risk with chemical risk is challenging for public health protection. Currently, the most commonly used disinfectants are chlorine, chlorine dioxide,chloramines and ozone. Here we provide an overview of chemical characterization, toxicity and analytical methods of 10 classes of DBPs, including trihalomethanes ( THMs), haloacefic acids ( HAAs), bromate ( BrO3- ), chlorite ( ClO2- ), haloacetonitriles (HANs), mutagen X (MX), halonitromethane ( HNMs), iodo acids (IAs), N-nitrosodimethylamines (NMs) and halobenzoquinones (HBQs). We will discuss the challenges and opportunities in the research of DBPs and health effects.%饮用水消毒过程中消毒剂与天然有机物(NOMs)反应生成消毒副产物(DBPs).本文针对氯、氯胺、二氧化氯、臭氧4种主要消毒方式产生的消毒副产物,综述了10类DBPs的化学特性、毒性和分析方法.具体包括:三卤甲烷(THMs)、卤乙酸(HAAs)、溴酸盐(BrO3-)、亚氯酸盐(CIO2-)、卤乙腈(HANs)、致诱变化合物(MX)、卤代硝基甲烷(HNMs)、碘代酸(Ias)、亚硝胺(NMs)以及卤代对苯醌(HBQs).

  8. Preparation of Anion-exchange Polymer-based Monolithic Column and Its Application in Ion Chromatography%阴离子交换聚合物整体柱的制备及其在离子色谱中的应用

    Institute of Scientific and Technical Information of China (English)

    李晶; 周琰春; 张嘉捷; 朱岩

    2012-01-01

    An anion-exchange monolithic column was prepared by a polymerization inside a stainless steel tube( 150 mm x 4. 6 i. d. mm) , taking glycidyl methacrylate( GMA) as functional monomer, ethylene dimethacrylate ( EDMA) as cross-linking agent and in the presence of 1, 4-butanediol, 1 -propanol and water as the porogen solvents and azobisisobutyronitrile ( AIBN) as a suitable initiator. Introduction of anion-exchange sites were achieved by reacting with tirmethylamine. Under the optimized reaction conditions and the modified conditions, the chromatographic characteristics of the prepared anion-exchange columns were further studied, and the separation of 5 common anions ( such as, acetate, bromate, nitrite, bromide, nitrate) on the prepared anion-exchange column was investigated. The prepared column exhibits more advantages such as simple preparation and low cost, and could be coupled with a commercial ion chromatography system directly, which will be favorable for more applications and investigations.%以偶氮二异丁腈( AIBN)为自由基引发剂,将甲基丙烯酸缩水甘油酯(GMA)单体和亚乙基二甲基丙烯酸酯(EDMA)交联剂通过原位聚合的方法,在不锈钢管柱(150 mm ×4.6 i.d.mm)中合成为具有一定机械性能和一定孔径结构的聚合物整体色谱柱;利用三甲胺动态修饰反应将整体柱改性为具有阴离子交换功能的整体型离子色谱分离柱.实验优化了制备条件和改性修饰条件,考察了相关离子交换容量、流体动力学参数和色谱性能等.采用直接紫外检测的方法,在205 nm检测波长下,常规阴离子乙酸根、溴酸根、亚硝酸根、溴离子、硝酸根均能得到较好的分离检测.结果表明,该阴离子交换整体色谱柱制备方法简便,成本较低,可以方便地与常规色谱系统进行联用,具有一定分析实用价值和较大的开发前景.

  9. An assessment of the influence of multiple stressors on the Vaal River, South Africa

    Science.gov (United States)

    Wepener, V.; van Dyk, C.; Bervoets, L.; O'Brien, G.; Covaci, A.; Cloete, Y.

    community structures. This was related to decreased fish health as demonstrated by increased oxidative stress due to exposure to metals such as copper and nickel as well as organic pollutants such as PCBs, HCHs and bromated flame retardants. This study clearly demonstrates the importance of the inclusion of higher tier assessment endpoints to elucidate the effects of multiple stressors in aquatic ecosystems. The study further allowed for the identification of specific effect endpoints that need to be included in future monitoring programmes such as viral immunoassays.

  10. Research of Compound Bread Additive%含酶复合面包添加剂的研制

    Institute of Scientific and Technical Information of China (English)

    李素云; 杨留枝; 江柯

    2011-01-01

    Wheat which was planted in China with moderate gluten content and bad muscle strength was researched by adding yeast foodstuff,emulsifier,oxidant,enzyme preparation,big bean powder of high activation,etc.This study examine the additive to the quality impact of bread and the best dosage.Through its single factor and orthogonal test,the best composition was: NH4Cl 0.045%,CaSO4 0.15%,CaH2PO4 0.1%,xylanses 0.003%,gluzyme 0.008%,sucrose fatty acid ester 0.2%,VC 0.1%,SSL0.4%,ADA 0.0045%,glycerin monostearate 0.2%,CaO2 0.08%,high activation old bean powder 1%.The results showed that the compound additives suited to Chinese wheat flour and contain no carcinogenic potassium bromate.%试验以面筋含量适中、筋力较差的国产小麦粉为供试面粉,添加酵母养料、乳化剂、氧化剂、酶制剂、高活性大豆粉等添加剂,研究其对面包质量的影响及最佳添加量。通过单因素及多因素正交试验法等进行试验得到的新型面包改良剂配方组成为:氯化铵0.045%、硫酸钙0.15%、磷酸氢钙0.1%、木聚糖酶0.003%、葡萄糖氧化酶0.008%、蔗糖酯0.2%、VC 0.1%、硬脂酰乳酸钠(SSL)0.4%、偶氮甲酰胺(ADA)0.0045%、单甘酯0.2%、CaO2 0.08%、高活性大豆粉1%、结果表明这种复合添加剂适合我国小麦粉并且不含致癌物溴酸钾。

  11. 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.

  12. 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.

  13. Investigation of the Oxidation Reaction of O3 with Bromide Ion in Aqueous Solution%水溶液中臭氧和溴离子的反应研究

    Institute of Scientific and Technical Information of China (English)

    俞潇婷; 张家辉; 潘循皙; 张仁熙; 侯惠奇

    2012-01-01

    The reaction mechanism of O3 with bromide ion in aqueous solution was studied by ion chromatography and UV-Vis spectrometry instruments.Ion chromatography analysis showed that only 10% of Br-which was oxidized by ozone was formed into bromate ion.The results demonstrated that the final products of the oxidation reaction were identified as Br2 and Br-3 except for BrO-3.The formation of Br-3 which was yielded from the reaction of Br2 with Br-was the major process in the reaction of Br-attacked by O3.The characteristic absorption spectrum of Br-3 with an absorption peak at 260 nm was also investigated.The results may provide helpful information about the mechanism of the oxidation reaction of Br-with O3 and fate of Br-or its derivatives in the environment by the oxidation processes.%为探明O3氧化Br-的反应机制,采用离子色谱、PDA紫外-可见光度仪研究了水中Br-被O3氧化的反应过程.离子色谱分析表明,被氧化的Br-中只有约10%被O3氧化成BrO3-.进一步研究表明,除了生成BrO3-外,Br-被O3氧化过程中还产生了Br2,Br2又与溶液中存在的Br-结合形成Br3-,并首次得到了Br3-的吸收光谱,测得Br3-的最大吸收峰λmax为260 nm,提出了Br-与O3的基元反应.该研究补充和完善了O3氧化Br-的反应机制,也为O3处理含Br-水时Br-的归趋提供了有益信息.

  14. 抗癌药物丙卡巴肼的合成工艺优化研究%Optimization of the synthetic process of antineoplastic drug procarbazine

    Institute of Scientific and Technical Information of China (English)

    刘志军; 陈河如

    2012-01-01

    目的 对丙卡巴肼的合成工艺进行优化.方法 以对甲苯甲酸为起始原料,经氯化亚砜回流得酰氯产物,再与异丙胺反应得N-异丙基对甲苯甲酰胺(3),化合物3经N-溴代丁二酰亚胺(NBS)溴代生成化合物4;甲基肼的硫酸盐在甲酸作用下生成中间体5;4与5反应得到抗癌药物丙卡巴肼.结果与结论 优化了丙卡巴肼的合成工艺,以5步反应、总收率45.9%、单步收率75%~90%合成目标化合物.所有化合物的结构均经1 H-NMR、13C-NMR和MS确证.%Optimization of the synthetic process of procarbazine has been conducted. Firstly, N-isopropyl-4-methylbenzamide(3) was synthesized from P-toluic acid by reaction with thionyl chloride,followed by ami-dation with isopropylamine. 3 was then transformed into N-isopropy1-4-bromomethylbenzamide (4) by bro-mation under light using iV-bromosuccimide(NBS). After changing methylhydrazine into N,N'-diformylm-ethylhydrazine(5),procarbazine was prepared from 4 and 5 in the presence of K2CO3. The process includes 5 steps with an overall yield of 45. 9% , in which the yield for each step lies between 75% to 90%. The structures of all the products were confirmed by 1 H-NMR, 13C-NMR and mass spectroscopy (MS ) respectively.

  15. Kinetic assessment and modeling of an ozonation step for full-scale municipal wastewater treatment: micropollutant oxidation, by-product formation and disinfection.

    Science.gov (United States)

    Zimmermann, Saskia G; Wittenwiler, Mathias; Hollender, Juliane; Krauss, Martin; Ort, Christoph; Siegrist, Hansruedi; von Gunten, Urs

    2011-01-01

    The kinetics of oxidation and disinfection processes during ozonation in a full-scale reactor treating secondary wastewater effluent were investigated for seven ozone doses ranging from 0.21 to 1.24 g O(3) g(-1) dissolved organic carbon (DOC). Substances reacting fast with ozone, such as diclofenac or carbamazepine (k(P, O3) > 10(4) M(-1) s(-1)), were eliminated within the gas bubble column, except for the lowest ozone dose of 0.21 g O(3) g(-1) DOC. For this low dose, this could be attributed to short-circuiting within the reactor. Substances with lower ozone reactivity (k(P, O3) scale measurements. Monte Carlo simulations showed that the observed differences were higher than model uncertainties. The overestimation of micropollutant oxidation was attributed to a protection of micropollutants from ozone attack by the interaction with aquatic colloids. Laboratory-scale batch experiments using wastewater from the same full-scale treatment plant could predict the oxidation of slowly-reacting micropollutants on the full-scale level within a factor of 1.5. The Rct value, the experimentally determined ratio of the concentrations of hydroxyl radicals and ozone, was identified as a major contribution to this difference. An increase in the formation of bromate, a potential human carcinogen, was observed with increasing ozone doses. The final concentration for the highest ozone dose of 1.24 g O(3) g(-1) DOC was 7.5 μg L(-1), which is below the drinking water standard of 10 μg L(-1). N-Nitrosodimethylamine (NDMA) formation of up to 15 ng L(-1) was observed in the first compartment of the reactor, followed by a slight elimination during sand filtration. Assimilable organic carbon (AOC) increased up to 740 μg AOC L(-1), with no clear trend when correlated to the ozone dose, and decreased by up to 50% during post-sand filtration. The disinfection capacity of the ozone reactor was assessed to be 1-4.5 log units in terms of total cell counts (TCC) and 0.5 to 2.5 log units for

  16. 冲击氯消毒控制建筑供水管道二次污染%Effect of Shock Chlorine Disinfection on Secondary Pollution in Building Water Supply System

    Institute of Scientific and Technical Information of China (English)

    王帅; 杨艳玲; 相坤; 李星; 赵锂; 陈永

    2016-01-01

    针对建筑小区的供水管道存在的生物作用等二次污染问题,研究了冲击氯消毒技术对DOC降解和硝化作用的控制效果以及对副产物溴酸盐的影响.结果表明,冲击氯消毒可有效控制DOC降解和硝化作用,生物降解作用明显减弱,可显著降低微生物超标的风险和威胁.停止冲击氯消毒后DOC降解和硝化作用逐步恢复,在冲击氯消毒后的第52 ~ 80天,DOC降解和硝化作用基本恢复到原有水平,因此有必要进行定期冲击氯消毒.冲击消毒后,BrO;浓度总体呈现增加的趋势,但在冲击氯消毒第80天后,供水管道的生物作用限制了BrO3-的生成,因此在进行冲击氯消毒时,应考虑供水管道中相关消毒副产物的变化趋势以及可能造成的化学安全性风险.%Aimed at solving the problem of secondary pollution in building water supply system,the effects of shock chlorine disinfection on dissolved organic carbon (DOC) biodegradation and biological nitrification as well as the existing bromate were investigated.The results showed that the shock chlorine disinfection was effective in controlling the DOC biodegradation and biological nitrification in the building water supply system.Meanwhile,the shock chlorine disinfection could significantly reduce the risk of bacteriological index.However,the biodegradation of DOC and biological nitrification could be restored to the original level on the 52nd to 80th day after chlorination.Therefore,the shock chlorine disinfection was required again.After shock chlorine disinfection,BrO3-concentrations showed an increase trend,and the biodegradation restricted the production of BrO3-concentration on the 80th day.Consequently,there should be paid more attention to the tendency of disinfection by-products and the risk of chemical safety during the shock chlorine disinfection.

  17. O3-BAC工艺处理太湖原水的技术研究和生产实践%Technical study and production practice of the O3-BAC to treat the raw water from Taihu lake

    Institute of Scientific and Technical Information of China (English)

    蒋福春; 张雪; 李琴; 陈玲瑚; 周洵

    2011-01-01

    以苏州相城水厂臭氧—生物活性炭(O3-BAC)工艺的应用情况为基础,分析和探讨该工艺实际应用效果和运行管理要求.结果表明:在常规工艺基础上,有机物去除率可提高20%~40%,氯消毒副产物降低近40%,出厂水水质稳定;O3-BAC工艺能有效应对藻类暴发和原水水质短暂突变等事件;水温对生物活性炭的处理效果影响较大,夏季较冬季理想;运行管理中应重点关注和解决活性炭寿命、溴酸盐、水质生物安全性及冬季高氨氮的处理等问题;针对太湖原水而言,O3-BAC工艺具有一定技术优势.%Based on the application of Ozone-Bilological Activated Carbon (O3 - BAC) in the Xiangcheng Water Treatment Plant of Suzhou, this paper analyzed and studied the practical application effects and operation requirements of this process. The results showed: based on conventional treatment, the organic removal efficiency would be improved by 20%~40%, chlorine disinfection byproducts would be reduced by 40%, and the effluent water quality was stable; O3 -BAC could handle the unexpected accidents, such as algae outbreak, and raw water quality temporal sudden deterio-ration; water temperature had a significant effects on BAC treatment, and the winter treatment was better than summer; during the operation, attention should be paid on the problems such as BAC lifetime, bromated, aqua-organism safety, and high ammonian nitrogen concentration in winter; according to the Taihu lake raw water, the O3 - BAC process had some technical advantages.

  18. 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

    2014-10-01

    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

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

    Institute of Scientific and Technical Information of China (English)

    李芳; 陆少鸣

    2013-01-01

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

  20. A Novel Method to Prepare Furfural from Xylose over Solid Acid Catalysts ( SO42-/TiO2)%固体酸催化剂SO42-/TiO2催化木糖脱水制备糠醛的新方法

    Institute of Scientific and Technical Information of China (English)

    吴树新; 孙涛

    2012-01-01

    探索了以固体超强酸SO42 -/TiO2为催化剂,催化木糖脱水环化制备糠醛的新方法.以TiCl4乙醇溶液(体积比1∶1)作为钛源、以浓氨水作为沉淀剂制备二氧化钛,硫酸溶液作为浸渍液,制备了SO42 -/TiO2固体超强酸.采用二溴化法(溴酸钠-溴化钠)对糠醛产量进行分析,研究了反应条件和催化剂制备过程中硫酸浸渍液浓度、焙烧温度等对糠醛产率的影响.结果表明,使用固体超强酸作催化剂,在最佳条件下,糠醛产率达到42.6%,而同样条件下用硫酸作催化剂糖醛产率只有15.6%.%Dehydration of xylose into furfural was performed with solid super acid(S042-/Ti02) as catalyst. The preparation of SO42-/TiO2 was made using TiCl4 in alcohol ( V(TiCl4) : V(alcohol) = 1:1) as titanium source,strong ammonia as precipitant and H2SO4 as impregnating solution. Dehydration of xylose into furfural was carried out in 25 mL degestion tube with oil-bath heating. The yield of furfural were determined in the method of two brominated (sodium bromate-sodium bromide).The conditions of preparation of furfural and the influence of its yield were researched. The results show that the catalyst is essential in the preparation of furfural for xylose dehydration reaction.The yield of furfural reaches to 42.6 % when solid super acid SO42-VTiO2 used as catalyst, while it is only 15.6 % at the same conditions using H2SO4 as catalyst.

  1. 双氧水预处理—连续滴定法测定铜电解液中砷锑%Determination of arsenic and antimony in copper electrolyte by hydrogen peroxide pretreatment-continuous titration method

    Institute of Scientific and Technical Information of China (English)

    肖发新; 曹岛; 毛建伟; 申晓妮; 杨涤心

    2012-01-01

    为解决铜电解液中砷锑铋之间复杂化学反应所引起的砷锑分析误差大的问题,在含砷锑矿石的砷锑连续滴定方法基础上,模拟了铜电解液中砷锑的存在环境,开发出适合于铜电解液砷锑测定的双氧水预处理-连续滴定法.首先采用适量双氧水消除As(Ⅲ),Sb(Ⅲ)对砷锑分析结果的影响,再依次加入硫酸和硫酸肼两次冒浓烟至瓶颈,冷却后于盐酸介质中,以次甲基兰-甲基橙为指示剂,先用硫酸铈标准溶液滴定Sb(Ⅲ),再用溴酸钾标准溶液滴定As(Ⅲ).实验表明,连续滴定法中,适宜的硫酸加入量为20 mL,发烟时间为5 min,滴定锑时的盐酸浓度为4.3 mol/L,温度为70℃,滴定砷时的盐酸浓度为1.8 mol/L,温度为80℃.采用本方法分析合成铜电解液,砷、锑的回收率分别为96%和104%.采用该方法分析铜电解生产线上铜电解液,测得结果与原子吸收光谱法吻合,相对标准偏差(n=6)小于1.2%.%In order to reduce analytical error resulted from the complicated chemical reaction among arsenic, antimony and bismuth in copper electrolyte, the environment of arsenic and antimony in copper electrolyte was simulated based on the continuous titration method of arsenic and antimony in arsenic-antimony ore,and a method for determination of arsenic and antimony in Copper electrolyte was developed by hydrogen peroxide pretreatment-continuous titration method. Firstly, the influences of As(Ⅲ) and Sb(Ⅲ} on analysis result of arsenic and antimony were eliminated by addtion of hydrogen peroxide. Then, sulfuric acid and hydrazine sulfate were added separately until the smoke emit to the bottle neck. After cooling down, Sb(Ⅲ} was titrated by eerie sulfate and As(Ⅲ} was titrated by potassium bro-mate in hydrochloric acid medium with methylene blue-methyl orange as indicator. The results showed that the optimal conditions in continuous titration were as follows: sulfuric acid dosage was 20 mL; smoking

  2. 紫菀的电化学指纹图谱研究%Electrochemical fingerprints of radix asteris

    Institute of Scientific and Technical Information of China (English)

    程旺兴; 陈振华; 陈佳; 程铭恩; 彭华胜; 方成武

    2012-01-01

    通过别洛索夫-扎鲍京斯基(B-Z)振荡反应研究不同产地中药紫菀鉴别的鉴别,将紫菀粉末加入H2SO4-Ce(SO4)2-CH2(COOH) 2-KBrO3中,干扰化学振荡体系,用电化学工作站记录数据,并对温度、紫菀用量等反应条件进行了考察,确定体系的最佳实验条件为12 mL(3.0 mol/L)H2SO4溶液、3 mL(0.1 mol/L)Ce(SO4)2溶液、6 mL(1.0 mol/L)CH2(COOH)2和3 mL(0.2 mol/L)KBrO3溶液,温度310 K、加入0.4g紫菀粉末,获得了不同产地紫菀的电化学指纹图谱.通过对不同产地中药材紫菀电化学指纹图谱的研究,发现不同产地的紫菀的指纹图谱主要参数有较大区别.该方法简便、准确、可靠,可方便的用于不同产地紫菀的鉴别.%The electrochemical fingerprints of radix asteris from different places have been studied by Belousov-Zhabotin-skii oscillation system. With adding power of Radix Asteris to chemical oscillation system of H2SO4-Ce ( SO4 )2-CH2-(COOH)2KBrO3 ,and the data of potential and time was recorded by the electrochemical workstation. The temperature of B-Z oscillation system,stirring speed,the added amount of radix asteris are studied also. The results showed that the optimum conditions were as follows; 12 mL 3.0 mol/L sulfuric acid,3 mL 0. 1 mol/L cerium( IV ) sulfate,6 mL 1. 0 mol/L malonic acid, 3 mL 0. 2 mol/L potassium bromate, reaction temperature 310 K,0. 4 g powder of radix asteris. The electrochemical fingerprints of radix asteris from different places showed significantly different characteristics, such as the maximum potential,induction time and oscillation lifetime,etc. So this method can be used to identify radix asteris from different origins and has the advantage of convenience, sensitivity and precision.

  3. Study on Chemical Fingerprints of Traditional Chinese Medicine Radix Paeoniae Rubra in Oscillation System%不同产地中药赤芍在振荡体系中的化学指纹图谱研究

    Institute of Scientific and Technical Information of China (English)

    程旺兴; 管艺; 陈佳; 方成武

    2011-01-01

    采用H2 SO4 - CH2 (COOH)2 - Ce2( SO4)3- KBrO3化学振荡体系,研究了中药赤芍的化学指纹图谱,并对温度、赤芍用量进行了考察,确定体系的最佳实验条件为12 mL 3.0 mol/L H2SO4溶液、6 mL 0.4 mol/LCH2( COOH)2溶液、3 mL 0.005 mol/L Ce2( SO4)3和3 mL 0.2 mol/L KBrO3溶液,温度35℃、加入0.4g的中药材粉末.通过对不同产地中药材赤芍(安徽毫州、山东菏泽、内蒙古赤峰、海拉尔)化学指纹图谱的研究,发现不同产地的中药材赤芍不仅具有明显不同的化学指纹图谱形状,而且主要参数也有很大区别.其中毫州赤芍的最高诱导时间较小(133.76 s),但振荡寿命最长(554.89 8);而海拉尔赤芍的诱导时间最长(214.t7 s),但振荡寿命最短(237.11 s).该化学指纹图谱可方便地用于不同产地中药材赤芍的区别和鉴定.%Chemical fingerprints of Radix Paeoniae Rubra( RPR) from different places of origin were studied by chemical oscillation system of H2SO4 - CH2 (COOH) 2 - Ce2 (SO4) 3 - KBrO3. Effects of various variables on the chemical oscillation system were studied. The optimal conditions were as fol lows; 12 mL 3. 0 mol/L sulfuric acid, 6 mL 0. 4 mol/L malonate, 3 mL 0. 005 mol/L cerium am monium sulfate, 3 mL 0. 2 mol/L sodium bromate and 0. 4 g RPR powder at 35 ℃. The results indi cated that, under the optimal conditions, the chemical fingerprints of RPR from different places of origin( Bozhou, Heze, Chifeng and Hailaer) showed significantly different characteristics, such as the maximum potential, induction time and oscillation lifetime, etc. The results also indicated that the RPR from Bozhou had the shortest induction time( 133. 76 s) , but the longest oscillation lifetime (554. 89 s). The RPR from Hailaer had the longest induction time(214. 17 s) , but the shortest os cillation lifetime(only 237. 11 s). The chemical fingerprints could be used to identify the origins of RPR. The method is simple, rapid and sensitive, and without

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

    Science.gov (United States)

    Shuai, Danmeng

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

  5. 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

  6. 柱前衍生化-气相色谱-质谱法定量测定食品中丙烯酰胺的含量%Quantification of acrylamide in foods by gas chromatography- mass spectrometry coupled with pro-column derivatization.

    Institute of Scientific and Technical Information of China (English)

    杨斯超; 张慧; 汪俊涵; 陈芳

    2011-01-01

    建立了气相色谱-质谱(GC-MS)定量测定食品中丙烯酰胺含量的分析方法.选择C-丙烯酰胺作为内标物.通过超纯水提取食品中的丙烯酰胺,经正已烷脱脂两次后,在酸性条件下选用溴化钾/溴酸钾为衍生剂进行衍生化反应,再采用乙酸乙酯进行液-液萃取两次,最后用三乙胺将丙烯酰胺转化为更稳定的产物2-溴丙烯酰胺,利用质谱检测器在选择离子扫描模式下测定2-溴丙烯酰胺.该方法在0.05~2.00 mg/kg范围具有良好的线性(r=0.999 5);检出限和定量限分别达到3 μg/kg和7 μg/kg;回收率范围为62.7%~65.5%.通过与前期建立的液相色谱-串联质谱(HPLC-MS/MS)方法进行对比,该法在薯片和面包样品中丙烯酰胺的检测结果略偏高,是一种可以用于常见食品中丙烯酰胺含量测定的分析方法.%The quantification of acrylamide in foods was investigated by gas chromatographymass spectrometry (GC-MS).In this method, 13C3-acrylamide was used as an internal standard.The samples were homogenized, defatted with hexane and extracted with ethyl acetate for twice.The derivatization of acrylamide into 2-bromopropenamide (2-BPA) was done using potassium bromide/potassium bromate at 4 ℃ for 90 min.Selective ion monitoring mode was chosen to monitor objective chromatography.This method had a good linearity between 0.05 -2.00 mg/kg (r2 = 0.999 5 ), and the limits of detection and quantification were 3 μg/kg and 7μg/kg, respectively.The recoveries of acrylamide were in the range of 62.7% - 65.5%.In order to confirm this GC-MS method, the acrylamide in foods was also determined by high performance liquid chromatography coupled to quadrupole tandem mass spectrometry (HPLC-MS/MS), which had been proved in our laboratory.The concentrations of acrylamide in the samples quantified by GC-MS were slightly higher than those detected by HPLC-MS/MS.This method can be used to quantify acrylamide in normal foods.

  7. Integrated Process of Polytetrafluoroethylene (PTFE)Hollow Fiber Membrane for Polluted Raw Water Treatment%受污染原水处理的聚四氟乙烯中空膜组合工艺

    Institute of Scientific and Technical Information of China (English)

    厉帅; 郭建宁; 范小江; 张亮; 王凌云; 张锡辉

    2014-01-01

    %,respectively;the turbidity of the effluent is below 0. 2 NTU,and the particle number in the effluent is less than 50 CNT/mL. The concentration of THMs,HAAs, bromate and formaldehyde in the effluent are below the standard limits,and the total bacterial counts and coliform counts are not detected. It can be concluded that the addition of ozone (O3/TOC=0. 6~0. 8)can mitigate membrane fouling substantially during the operation and reduce the frequency of membrane cleaning to the half;dosage of 7 ~9 mg O3/L can eliminate membrane fouling gradually without taking out the membrane,thus chemical cleaning frequencies are decreased.

  8. 宽浓度范围水碘的碱性高锰酸钾氧化光度测定方法研究%Method for the determination of broad concentration range of iodide in drinking water by spectrophotometry with alkaline potassium permanganate oxidation

    Institute of Scientific and Technical Information of China (English)

    张亚平; 黄嫣红; 林丽卿

    2009-01-01

    water. Results The linear range of the calibration curve of the new method for iodine was 0-1200 μg/L and the linear correlative coefficient was 0.9998. The detection limit for iodine was 4 μg/L. Results of 6 times repeated determination of water samples with iodine concentration of 76.6, 207.8, 560.4 μg/L showed that the relative standard deviations(RSD) were all under 1%. The recovery of standard addition for iodine added in 8 water samples of different iodide concentration levels was 97.0% (485.2/500.0) - 102.5% (102.5/100.0). Interference of hexavalent chromium(Cr~(6+)) in water was eliminated when treated with ferrous reagent. Interference of bromate (BrO_3~-) in water was eliminated when treated with potassium bromide and nitrite sodium reagent. Zero point two mg/L Cr~(6+), 0.1 mg/L BrO_3~- in water were noninterference. Conclusion This method can be easily performed with good precision and accuracy and has broad detection concentration range, which is suitable for measuring iodide in drinking water.

  9. 臭氧接触池臭氧投加方式的优化%Optimization of Ozone Distribution Method in the Ozone Contactor

    Institute of Scientific and Technical Information of China (English)

    袁蓉芳; 田烨; 施春红; 周北海; 顾军农; 张春雷

    2013-01-01

    effluent water was too high for the following process.The mass transfer efficiency of ozone in the water was 78.1%,and the removal efficiency of oganics was 47.5% when three-point aeration was used,with the proportion of 3∶ 3∶ 1.When humic acid of 3 mg/L was added in the water samples,the mass transfer efficiency of ozone was 76.8%,and the removal efficiency of oganics was 40.3% using the same method.The O3 content in the effluent water was 0.26 mg/L,which would not destroy the biofilm on the surface of the activated carbon in biological activated carbon progress.At the proportion of 3∶ 3∶ 1,the utilization ratio of ozone value was the highest (60.1%),and the generation amount of bromate was the lowest.Therefore,the best method of gas distribution in ozone contactor was three-point aeration,with the proportion of 3∶ 3∶ 1.