WorldWideScience

Sample records for chlorine oxides

  1. Kinetic study of neodymium oxide chlorination with gaseous chlorine

    Energy Technology Data Exchange (ETDEWEB)

    Bosco, Marta V., E-mail: marta.bosco@cab.cnea.gov.ar [Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET) (Argentina); Fouga, Gaston G. [Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET) (Argentina); Complejo Tecnologico Pilcaniyeu, Comision Nacional de Energia Atomica, Avenida Bustillo 9500, CP 8400 San Carlos de Bariloche (Argentina); Bohe, Ana E. [Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET) (Argentina); Complejo Tecnologico Pilcaniyeu, Comision Nacional de Energia Atomica, Avenida Bustillo 9500, CP 8400 San Carlos de Bariloche (Argentina); Centro Regional Universitario Bariloche, Universidad Nacional del Comahue, CP 8400 San Carlos de Bariloche (Argentina)

    2012-07-20

    Highlights: Black-Right-Pointing-Pointer We analyze the kinetics of the neodymium oxide chlorination reactions. Black-Right-Pointing-Pointer For temperatures below 425 Degree-Sign C the system is under chemical control. Black-Right-Pointing-Pointer The formation of oxychloride progresses through a nucleation and growth mechanism. Black-Right-Pointing-Pointer A reaction order of 0.40 with respect to chlorine partial pressure was determined. Black-Right-Pointing-Pointer An activation energy of 161 {+-} 4 kJ mol{sup -1} was determined. - Abstract: The kinetics of the chlorination of neodymium oxide has been investigated by thermogravimetry between 312 Degree-Sign C and 475 Degree-Sign C, and for partial pressures of chlorine ranging from 10 kPa to 50 kPa. The starting temperature for the reaction of neodymium oxide with chlorine was determined to be about 250 Degree-Sign C, leading to neodymium oxychloride as product. The results showed that, for temperatures below 425 Degree-Sign C, the system is under chemical control and the formation of the oxychloride progresses through a nucleation and growth mechanism. The influence of chlorine mass transport through the bulk gas phase and through the boundary layer on the overall reaction rate was analyzed. In the absence of these two mass-transfer steps, a reaction order of 0.39 with respect to chlorine partial pressure, and an activation energy of 161 {+-} 4 kJ mol{sup -1} were determined. A complete rate equation has been successfully developed.

  2. Effects of chlorine content and position of chlorinated phenols on their oxidation kinetics by potassium permanganate

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    Chlorine content and position of chlorinated phenols have many significant effects on the reactivity of oxido-reduction. The effects of chlorine content and position of chlorinated phenols on their oxidation kinetics by potassium permanganate were evaluated through different kinetics studies. Since chlorine was an electron withdrawing atom, the substitution of chlorine on the aromatic ring decreased the oxidation rate constant by σ-electron withdrawing conductive effect; at the same time, the substitution of chlorine at ortho or para position on the aromatic ring increased the oxidation rate constant by π-electron donating conjugative effect, and the conjugative effect could counteract the negative impact of the conductive effect to some extent. On the other hand, the substitution of chlorine at ortho position on the aromatic ring decreased the oxidation rate constant by steric hindrance effect. The oxidation rate constants of phenol and chlorinated phenols studied decreased as follow order: 4-chlorophenol>2,4-dichlorophenol>phenol>2,6-dichlorophenol.

  3. Halogenase-Inspired Oxidative Chlorination Using Flavin Photocatalysis.

    Science.gov (United States)

    Hering, Thea; Mühldorf, Bernd; Wolf, Robert; König, Burkhard

    2016-04-18

    Chlorine gas or electropositive chlorine reagents are used to prepare chlorinated aromatic compounds, which are found in pharmaceuticals, agrochemicals, and polymers, and serve as synthetic precursors for metal-catalyzed cross-couplings. Nature chlorinates with chloride anions, FAD-dependent halogenases, and O2 as the oxidant. A photocatalytic oxidative chlorination is described based on the organic dye riboflavin tetraacetate mimicking the enzymatic process. The chemical process allows within the suitable arene redox potential window a broader substrate scope compared to the specific activation in the enzymatic binding pocket.

  4. Chlorination and Carbochlorination of Cerium Oxide

    International Nuclear Information System (INIS)

    The chlorination and carbochlorination of cerium oxide were studied by thermogravimetry under controlled atmosphere (TG) in the 7000C 9500C temperature range.Both reactants and products were analyzed by X-ray diffraction (RX), scanning electronic microscopy (SEM) and energy dispersive spectroscopy (EDS). Thermodynamic calculations were performed by computer assisted software.The chlorination starts at a temperature close to 8000C.This reaction involves the simultaneous formation and evaporation of CeCl3.Both processes control the reaction rate and their kinetic may not be easily separated.The apparent chlorination activation energy in the 8500C-9500C temperature range is 172 to 5 kJ/ mole.Carbon transforms the CeO2-Cl2 into a more reactive system: CeO2-C-Cl2, where the effects of the carbon content, total flow rate and temperature were analyzed.The carbochlorination starting temperature is 7000C.This reaction is completed in one step controlled by mass transfer with an apparent activation energy of 56 to 5 kJ/mole in the 8500C-9500C temperature range

  5. Oxidative elimination of cyanotoxins: comparison of ozone, chlorine, chlorine dioxide and permanganate.

    Science.gov (United States)

    Rodríguez, Eva; Onstad, Gretchen D; Kull, Tomas P J; Metcalf, James S; Acero, Juan L; von Gunten, Urs

    2007-08-01

    As the World Health Organization (WHO) progresses with provisional Drinking Water Guidelines of 1 microg/L for microcystin-LR and a proposed Guideline of 1 microg/L for cylindrospermopsin, efficient treatment strategies are needed to prevent cyanotoxins such as these from reaching consumers. A kinetic database has been compiled for the oxidative treatment of three cyanotoxins: microcystin-LR (MC-LR), cylindrospermopsin (CYN), and anatoxin-a (ANTX) with ozone, chlorine, chlorine dioxide and permanganate. This kinetic database contains rate constants not previously reported and determined in the present work (e.g. for permanganate oxidation of ANTX and chlorine dioxide oxidation of CYN and ANTX), together with previously published rate constants for the remaining oxidation processes. Second-order rate constants measured in pure aqueous solutions of these toxins could be used in a kinetic model to predict the toxin oxidation efficiency of ozone, chlorine, chlorine dioxide and permanganate when applied to natural waters. Oxidants were applied to water from a eutrophic Swiss lake (Lake Greifensee) in static-dose testing and dynamic time-resolved experiments to confirm predictions from the kinetic database, and to investigate the effects of a natural matrix on toxin oxidation and by-product formation. Overall, permanganate can effectively oxidize ANTX and MC-LR, while chlorine will oxidize CYN and MC-LR and ozone is capable of oxidizing all three toxins with the highest rate. The formation of trihalomethanes (THMs) in the treated water may be a restriction to the application of sufficiently high-chlorine doses.

  6. Chlorine dioxide as an oxidant for organoboron compounds

    International Nuclear Information System (INIS)

    Practicability of using chlorine dioxide aqueous solution as an oxidant for terpene organoboron compounds prepared by hydroborating (+)α-pinene (1) and (-)β-pinene (2) is studied. By the methods of IR spectroscopy and 13C NMR it is shown that products of 1 and 2 oxidation are (-)-isopinocampheol and (-)-cis-myrtanol, which are formed with a high yield. In terms of its efficiency chlorine dioxide is no worse than hydrogen peroxide in reactions of organoboric compounds oxidation

  7. Advantages and disadvantages of chemical oxidation and disinfection by ozone and chlorine dioxide

    Energy Technology Data Exchange (ETDEWEB)

    Fiessinger, F.; Richard, Y.; Montiel, A.; Musquere, P.

    1981-04-01

    Ozone and chlorine dioxide present definite advantages and disadvantages over chlorination. Chlorination, particularly for the removal of ammonia and the maintenance of a disinfectant residual in the distribution system has decisive advantages and will be difficult to replace. Ozone and chlorine dioxide seem to produce fewer carcinogenic by-products but the risk for acute toxicity, especially from the chlorites which follow chlorine dioxide, is higher than with chlorine. Chlorine dioxide and more particularly ozone should be considered as useful complements to chlorination, but no strong oxidative treatment should be applied before most of the organic matter has been removed.

  8. Oxidation of pharmaceuticals by chlorine dioxide in wastewater effluent.

    OpenAIRE

    Alcalá Borao, Raquel

    2015-01-01

    The presence of pharmaceuticals in the environment has raised an emerging interest due to the fact that they pose negative environmental impact and health hazards related to long-term toxicity effects. As conventional treatments are not able to totally remove these substances it is necessary to seek for alternative advanced technologies such as oxidation with chlorine dioxide (ClO2). The objective of this master thesis is thus to find the most optimal dose – reaction time of ClO2 for the oxid...

  9. Detection of chlorinated methanes by tin oxide gas sensors.

    Science.gov (United States)

    Park, S H; Son, Y C; Shaw, B R; Creasy, K E; Suib, S L

    2001-08-01

    Tin oxide thin films prepared by thermal oxidation of Sn films were used for the detection of chlorinated methanes (CH2Cl2, CHCl3 and CCl4). This resulted in better chemical selectivity, sensitivity, response speed and detection limit than seen with previous detectors. The temperature dependence of the sensing of 1% CCl4 gas was studied and the best sensing behavior was observed at 300 degrees C. The films showed different chemical selectivity in both speed and direction of sensing response to each gas and were stable for more than 3 weeks under operating conditions. The films showed rapid gas sensing (<40 s to reach 90% of full response) and low detection limits (< 4 ppm CCl4). The role of oxygen in the detection of chlorinated methanes and in resistance changes without chlorinated methanes was also studied. The changes at the surface of the film after gas sensing were examined using scanning electron microscopy with energy-dispersive X-ray spectrometry. PMID:11534610

  10. Removal of C.I. Reactive Red 2 by low pressure UV/chlorine advanced oxidation.

    Science.gov (United States)

    Wu, Qianyuan; Li, Yue; Wang, Wenlong; Wang, Ting; Hu, Hongying

    2016-03-01

    Azo dyes are commonly found as pollutants in wastewater from the textile industry, and can cause environmental problems because of their color and toxicity. The removal of a typical azo dye named C.I. Reactive Red 2 (RR2) during low pressure ultraviolet (UV)/chlorine oxidation was investigated in this study. UV irradiation at 254nm and addition of free chlorine provided much higher removal rates of RR2 and color than UV irradiation or chlorination alone. Increasing the free chlorine dose enhanced the removal efficiency of RR2 and color by UV/chlorine oxidation. Experiments performed with nitrobenzene (NB) or benzoic acid (BA) as scavengers showed that radicals (especially OH) formed during UV/chlorine oxidation are important in the RR2 removal. Addition of HCO3(-) and Cl(-) to the RR2 solution did not inhibit the removal of RR2 during UV/chlorine oxidation. PMID:26969069

  11. Hydrothermal Synthesis of Indium Tin Oxide Nanoparticles without Chlorine Contamination

    International Nuclear Information System (INIS)

    Indium tin oxide (In2Sn1-xO5-y) nanoparticles were synthesized by hydrothermal method from stable indium tin acetylacetone complexes and post annealing at 600 .deg. C. The absence of chlorine ions shortened the synthesis process, decreased the particle agglomeration and improved the particle purity. The introduced complexing ligand acetylacetone decreased the obtained nanoparticle size. The improved powder properties accelerated the sintering of the In2Sn1-xO5-y nanoparticles and reached a relative density of 96.4% when pressureless sintered at 1400 .deg. C

  12. Chlorine

    Energy Technology Data Exchange (ETDEWEB)

    Talmage, Sylvia Smith [ORNL

    2009-01-01

    Following a brief description of the use of chlorine as a chemical warfare agent in World War I, this chapter summarizes physical and chemical data and recent clinical and controlled laboratory studies on the irritant and lethal effects of chlorine. The mechanism of toxicity for both irritation and lethal effects is described. The mathematical relationship between concentration and exposure duration for a set endpoint is given for both an irritancy response and mortality. This information can be used to assist in time-scaling for the set endpoint to other exposure durations. Risk assessment addresses the potential for greater effects in sensitive populations such as asthmatics. A concentration of 0.5 ppm for up to 8 hours is a no-adverse-effect concentration in most sensitive subjects; whereas, a concentration of 1.0 ppm induces some sensory irritation and transient changes in respiratory tract airflow parameters. Treatment and intervention of exposed individuals is dependent upon symptoms

  13. Oxidation of pharmaceuticals by chlorine dioxide in biologically treated wastewater

    DEFF Research Database (Denmark)

    Hey, G.; Grabic, R.; Ledin, A.;

    2012-01-01

    nitrogen removal (low COD) and one without (high COD). About one third of the tested APIs resisted degradation even at the highest ClO2 dose (20mg/L), while others were reduced by more than 90% at the lowest ClO2 level (0.5mg/L). In the low COD effluent, more than half of the APIs were oxidized at 5mg/L Cl......O2, while in high COD effluent a significant increase in API oxidation was observed after treatment with 8mg/L ClO2. This study illustrates the successful degradation of several APIs during treatment of wastewater effluents with chlorine dioxide....

  14. Fluorine and chlorine determination in oxides and metals by ion chromatography

    International Nuclear Information System (INIS)

    Method for simultaneous determination of fluorine and chlorine microquantitie in tantalum, uranium and plutonium oxides, based on combined methods of pyrohydrolysis (1000-1100 deg C) and two-column ion chromatography with conductometric detection is suggested. The relative root-mean-square deviation of determination error is 0.2, the fluorine and chlorine content being 5·10-4 mass%

  15. Chlorine dioxide-facilitated oxidation of the azo dye amaranth.

    Science.gov (United States)

    Nadupalli, S; Koorbanally, N; Jonnalagadda, S B

    2011-10-27

    The oxidation reaction of amaranth (trisodium 2-hydroxy-1-(4-sulfonato-1-naphthylazo)naphthalene-3,6-disulfonate or AM(-)) by chlorine dioxide (ClO(2)) in aqueous conditions was investigated in detail. The major reaction products immediately after decolorization of AM(-) were 1,2-naphthoquinone disulfonate sodium salt and 1,4-napthalenedione. The reaction had first-order dependence on both AM(-) and ClO(2). The rate-limiting step involved the reaction between AM(-) and OH(-) ions. The role of hydroxide ion as a catalyst was established. The second-order rate constant increased with pH, from (19.8 ± 0.9) M(-1) s(-1) at pH 7.0, (97.1 ± 2.3) M(-1) s(-1) at pH 8.0 to (132.5 ± 2.8) M(-1) s(-1) at pH 9.0. In the pH range of 6.0-7.5, the catalytic constant for OH(-) ion was 4.0 × 10(9) M(-2) s(-1). The energy and entropy of activation values for the reaction were 50.0 kJ mol(-1) and -658.7 J K(-1) mol(-1), respectively. A probable reaction mechanism was elucidated and was validated by simulations.

  16. Effect of sulfur dioxide on indium (3) oxide chlorination

    International Nuclear Information System (INIS)

    On the basis of thermodynamic calculations and kinetic investigations, it is established that in the temperature range from 550 to 800 deg C in the In2O3-Cl2-SO2 system coupled reactions of InCl3 and In2(SO4)3 formation accompanying by further In2(SO4)3 chlorination with gaseous chlorine are main processes, SO2 accelerates considerably In2O3 chlorination at a temperature below 800 deg C, its influence on the process of chloride sublimation at a temperature higher than 800 deg C is not so noticeable

  17. The mechanism for free chlorine oxidation of reduced manganese in mixed-media filters

    OpenAIRE

    Occiano, Suzanne

    1988-01-01

    The removal mechanisms of soluble manganese [Mn (1l)] through mixed-media filters were investigated. Experimentation was directed toward the continuous supply of an oxidant during column filter studies. Free chlorine (HOCl, OC1â ) was chosen to increase soluble manganese removal efficiency because chlorine is readily available and inexpensive. Filter media from four different water treatment plants were used in this study. Continuous-flow filter columns were operated in the presence and a...

  18. Kinetics of the oxidation of cylindrospermopsin and anatoxin-a with chlorine, monochloramine and permanganate.

    Science.gov (United States)

    Rodríguez, Eva; Sordo, Ana; Metcalf, James S; Acero, Juan L

    2007-05-01

    Cyanobacteria produce toxins that may contaminate drinking water sources. Among others, the presence of the alkaloid toxins cylindrospermopsin (CYN) and anatoxin-a (ANTX) constitutes a considerable threat to human health due to the acute and chronic toxicity of these compounds. In the present study, not previously reported second-order rate constants for the reactions of CYN and ANTX with chlorine and monochloramine and of CYN with potassium permanganate were determined and the influence of pH and temperature was established for the most reactive cases. It was found that the reactivity of CYN with chlorine presents a maximum at pH 7 (rate constant of 1265 M(-1)s(-1)). However, the oxidation of CYN with chloramine and permanganate are rather slow processes, with rate constants <1 M(-1)s(-1). The first chlorination product of CYN was found to be 5-chloro-CYN (5-Cl-CYN), which reacts with chlorine 10-20 times slower than the parent compound. The reactivity of ANTX with chlorine and chloramines is also very low (k<1M(-1)s(-1)). The elimination of CYN and ANTX in surface water was also investigated. A chlorine dose of 1.5 mg l(-1) was enough to oxidize CYN almost completely. However, 3 mg l(-1) of chlorine was able to remove only 8% of ANTX, leading to a total formation of trihalomethanes (TTHM) at a concentration of 150 microg l(-1). Therefore, chlorination is a feasible option for CYN degradation during oxidation and disinfection processes but not for ANTX removal. The permanganate dose required for CYN oxidation is very high and not applicable in waterworks.

  19. Sulfur dioxide effect on cadmium and zinc oxide interaction with chlorine

    International Nuclear Information System (INIS)

    Comparison of electrophysical properties of cadmium and zinc oxides with kinetic regularities of their interaction with Cl2 and SO2 was conducted. It is shown that SO2 presence in gas phase leads to retardation of chlorination of both oxides. In the case of CdO the effect of SO2 is manifested more clearly

  20. Electrochemical chlorine evolution at rutile oxide (110) surfaces

    DEFF Research Database (Denmark)

    Hansen, Heine Anton; Man, Isabela Costinela; Studt, Felix;

    2010-01-01

    of the oxygen binding energy, giving rise to a Sabatier volcano. By combining the surface phase diagram and the volcano describing the catalytic activity, we find that the reaction mechanism differs depending on catalyst material. The flexibility in reaction path means that the chlorine evolution activity...

  1. Kinetics and pathways of ibuprofen degradation by the UV/chlorine advanced oxidation process.

    Science.gov (United States)

    Xiang, Yingying; Fang, Jingyun; Shang, Chii

    2016-03-01

    The UV/chlorine advanced oxidation process (AOP), which forms reactive species such as hydroxyl radicals (HO) and reactive chlorine species (RCS) such as chlorine atoms (Cl) and Cl2(-), is being considered as an alternative to the UV/H2O2 AOP for the degradation of emerging contaminants. This study investigated the kinetics and pathways of the degradation of a recalcitrant pharmaceutical and personal care product (PPCP)-ibuprofen (IBP)-by the UV/chlorine AOP. The degradation of IBP followed the pseudo first-order kinetics. The first-order rate constant was 3.3 times higher in the UV/chlorine AOP than in the UV/H2O2 AOP for a given chemical molar dosage at pH 6. The first-order rate constant decreased from 3.1 × 10(-3) s(-1) to 5.5 × 10(-4) s(-1) with increasing pH from 6 to 9. Both HO and RCS contributed to the degradation, and the contribution of RCS increased from 22% to 30% with increasing pH from 6 to 9. The degradation was initiated by HO-induced hydroxylation and Cl-induced chlorine substitution, and sustained through decarboxylation, demethylation, chlorination and ring cleavage to form more stable products. Significant amounts of chlorinated intermediates/byproducts were formed from the UV/chlorine AOP, and four chlorinated products were newly identified. The yield of total organic chlorine (TOCl) was 31.6 μM after 90% degradation of 50 μM IBP under the experimental conditions. The known disinfection by-products (DBPs) comprised 17.4% of the TOCl. The effects of water matrix in filtered drinking water on the degradation were not significant, demonstrating the practicality of the UV/chlorine AOP for the control of some refractory PPCPs. However, the toxicity of the chlorinated products should be further assessed.

  2. Oxidation of pharmaceuticals by chlorine dioxide in biologically treated wastewater

    OpenAIRE

    Hey, G.; Grabic, R.; Ledin, A.; la Cour Jansen, J; Andersen, H R

    2012-01-01

    Biologically treated wastewater spiked with a mixture of 56 active pharmaceutical ingredients (APIs) was treated with 0–20mg/L chlorine dioxide (ClO2) solution in laboratory-scale experiments. Wastewater effluents were collected from two wastewater treatment plants in Sweden, one with extended nitrogen removal (low COD) and one without (high COD). About one third of the tested APIs resisted degradation even at the highest ClO2 dose (20mg/L), while others were reduced by more than 90% at the l...

  3. SIMULATING THE IN-SITU OXIDATIVE TREATMENT OF CHLORINATED ETHYLENES BY POTASSIUM PERMANGANATE

    Science.gov (United States)

    In recent years, MnO{sub}4 oxidation of chlorinated ethylenes (PCE, TCE, and DCE) has emerged as a potentially useful approach for destroying these componds in water. Recently, more applied studies have looked at whether KMnO{sub}4 could be used in remediating sites contaminated ...

  4. Corrosion behavior of silicon nitride, magnesium oxide, and several metals in molten calcium chloride with chlorine

    International Nuclear Information System (INIS)

    In this paper corrosion studies are described in a molten calcium chloride environment sparged with chlorine gas at 850 degrees C, both in the melt and in the gas phase above the salt, in support of efforts at Westinghouse Savannah River Company to develop more resistant materials of construction for molten salt processing of plutonium. Corrosion rates and electron microscope analyses are reported for Inconel alloys 601 and 617, tantalum, tungsten, magnesium oxide, and silicon nitride. Silicon nitride exhibited the greatest resistance, showing 2 · h loss in both melt and vapor None of the metallic coupons withstood the chlorine vapor environment, although Inconel indicated resistance immersed in the melt if protected from chlorine gas

  5. Chlorine Gas Exposure Causes Systemic Endothelial Dysfunction by Inhibiting Endothelial Nitric Oxide Synthase–Dependent Signaling

    OpenAIRE

    Honavar, Jaideep; Samal, Andrey A.; Bradley, Kelley M.; Brandon, Angela; Balanay, Joann; Squadrito, Giuseppe L.; MohanKumar, Krishnan; Maheshwari, Akhil; Postlethwait, Edward M.; Matalon, Sadis; Patel, Rakesh P.

    2010-01-01

    Chlorine gas (Cl2) exposure during accidents or in the military setting results primarily in injury to the lungs. However, the potential for Cl2 exposure to promote injury to the systemic vasculature leading to compromised vascular function has not been studied. We hypothesized that Cl2 promotes extrapulmonary endothelial dysfunction characterized by a loss of endothelial nitric oxide synthase (eNOS)-derived signaling. Male Sprague Dawley rats were exposed to Cl2 for 30 minutes, and eNOS-depe...

  6. Contrasting effects of sulfur dioxide on cupric oxide and chloride during thermochemical formation of chlorinated aromatics.

    Science.gov (United States)

    Fujimori, Takashi; Nishimoto, Yoshihiro; Shiota, Kenji; Takaoka, Masaki

    2014-12-01

    Sulfur dioxide (SO2) gas has been reported to be an inhibitor of polychlorinated dibenzo-p-dioxins and furans (PCDD/Fs) formation in fly ash. However, other research has suggested little or no inhibitory effect of SO2 gas. Although these studies focused on reactions between SO2 gas and gas-phase chlorine (Cl) species, no attention was paid to thermochemical gas-solid reactions. In this study, we found contrasting effects of SO2 gas depending on the chemical form of copper (CuO vs CuCl2) with a solid-phase inorganic Cl source (KCl). Chlorinated aromatics (PCDD/Fs, polychlorinated biphenyls, and chlorobenzenes) increased and decreased in model fly ash containing CuO + KCl and CuCl2 + KCl, respectively, with increased SO2 injection. According to in situ Cu K-edge and S K-edge X-ray absorption spectroscopy, Cl gas and CuCl2 were generated and then promoted the formation of highly chlorinated aromatics after thermochemical reactions of SO2 gas with the solid-phase CuO + KCl system. In contrast, the decrease in aromatic-Cls in a CuCl2 + KCl system with SO2 gas was caused mainly by the partial sulfation of the Cu. The chemical form of Cu (especially the oxide/chloride ratio) may be a critical factor in controlling the formation of chlorinated aromatics using SO2 gas.

  7. Chlorination of UO2, PuO2, and rare-earth oxides using ZrCl4

    International Nuclear Information System (INIS)

    A new chlorination method using ZrCl4, which has a high reactivity with oxygen, has been investigated for more efficient oxide treatment. After actinide oxides are chlorinated and dissolved in a molten salt bath, actinide metals can be selectively collected using the electrorefining process. This process is well suited for pyrochemical reprocessing of metallic fuels. In LiCl-KCI eutectic melts, rare-earth oxides (Y2O3, La2O3, CeO2, and Nd2O3) and actinide oxides (UO2 and PuO2) were chlorinated by adding ZrCl4. As a result, rare-earth and actinide elements were dissolved into the salt as trivalent ions and ZrO2 was precipitated. When an excess of ZrCI4 was added, oxides in powder form were completely chlorinated in five hours. It was demonstrated that the ZrCI4 chlorination method, free from corrosive gas such as chlorine, was very simple and useful. (author)

  8. Reduction of excess sludge production in sequencing batch reactor through incorporation of chlorine dioxide oxidation

    International Nuclear Information System (INIS)

    In this study, chlorine dioxide (ClO2) instead of chlorine (Cl2) was proposed to minimize the formation of chlorine-based by-products and was incorporated into a sequencing batch reactor (SBR) for excess sludge reduction. The results showed that the sludge disintegrability of ClO2 was excellent. The waste activated sludge at an initial concentration of 15 g MLSS/L was rapidly reduced by 36% using ClO2 doses of 10 mg ClO2/g dry sludge which was much lower than that obtained using Cl2 based on similar sludge reduction efficiency. Maximum sludge disintegration was achieved at 10 mg ClO2/g dry sludge for 40 min. ClO2 oxidation can be successfully incorporated into a SBR for excess sludge reduction without significantly harming the bioreactor performance. The incorporation of ClO2 oxidation resulted in a 58% reduction in excess sludge production, and the quality of the effluent was not significantly affected.

  9. EVALUATING ARSENIC AND MANGANESE REMOVAL FROM WATER BY CHLORINE OXIDATION FOLLOWED BY CLARIFICATION

    Directory of Open Access Journals (Sweden)

    V. G. R. Pires

    2015-06-01

    Full Text Available AbstractThis paper investigates the simultaneous removal of arsenic [As(V or As(III] and manganese [Mn(II] from natural waters of low and high turbidity by clarification (with polyaluminum chloride and aluminum sulfate as primary coagulants associated or not with chlorine pre-oxidation. The results showed that the clarification process exhibited low Mn(II removal, that varied from 6% to 18% and from 19% to 27% for natural waters of low and high turbidity, respectively. The use of chlorine as pre-oxidant increased Mn(II removal up to 77% and was associated with the formation of birnessite. Regarding As(V removal by clarification, particularly for high turbidity water, a concentration lower than that established by the National Drinking Water Quality Standards (10 μg.L-1 was achieved in almost all tests. Oxidation preceding the clarification led to AsIII removal efficiencies from 80% to 90% for both coagulants and types of water.

  10. Literature information applicable to the reaction of uranium oxides with chlorine to prepare uranium tetrachloride

    International Nuclear Information System (INIS)

    The reaction of uranium oxides and chlorine to prepare anhydrous uranium tetrachloride (UCl4) are important to more economical preparation of uranium metal. The most practical reactions require carbon or carbon monoxide (CO) to give CO or carbon dioxide (CO2) as waste gases. The chemistry of U-O-Cl compounds is very complex with valances of 3, 4, 5, and 6 and with stable oxychlorides. Literature was reviewed to collect thermochemical data, phase equilibrium information, and results of experimental studies. Calculations using thermodynamic data can identify the probable reactions, but the results are uncertain. All the U-O-Cl compounds have large free energies of formation and the calculations give uncertain small differences of large numbers. The phase diagram for UCl4-UO2 shows a reaction to form uranium oxychloride (UOCl2) that has a good solubility in molten UCl4. This appears more favorable to good rates of reaction than reaction of solids and gases. There is limited information on U-O-Cl salt properties. Information on the preparation of titanium, zirconium, silicon, and thorium tetrachlorides (TiCl4, ZrCl4, SiCl4, ThCl4) by reaction of oxides with chlorine (Cl2) and carbon has application to the preparation of UCl4

  11. Active chlorine and nitric oxide formation from chemical rocket plume afterburning

    Science.gov (United States)

    Leone, D. M.; Turns, S. R.

    1994-01-01

    Chlorine and oxides of nitrogen (NO(x)) released into the atmosphere contribute to acid rain (ground level or low-altitude sources) and ozone depletion from the stratosphere (high-altitude sources). Rocket engines have the potential for forming or activating these pollutants in the rocket plume. For instance, H2/O2 rockets can produce thermal NO(x) in their plumes. Emphasis, in the past, has been placed on determining the impact of chlorine release on the stratosphere. To date, very little, if any, information is available to understand what contribution NO(x) emissions from ground-based engine testing and actual rocket launches have on the atmosphere. The goal of this work is to estimate the afterburning emissions from chemical rocket plumes and determine their local stratospheric impact. Our study focuses on the space shuttle rocket motors, which include both the solid rocket boosters (SRB's) and the liquid propellant main engines (SSME's). Rocket plume afterburning is modeled employing a one-dimensional model incorporating two chemical kinetic systems: chemical and thermal equilibria with overlayed nitric oxide chemical kinetics (semi equilibrium) and full finite-rate chemical kinetics. Additionally, the local atmospheric impact immediately following a launch is modeled as the emissions diffuse and chemically react in the stratosphere.

  12. Oxidation of diclofenac by aqueous chlorine dioxide: identification of major disinfection byproducts and toxicity evaluation.

    Science.gov (United States)

    Wang, Yingling; Liu, Haijin; Liu, Guoguang; Xie, Youhai

    2014-03-01

    Diclofenac (DCF), a synthetic non-steroidal anti-inflammatory drug, is one of the most frequently detected pharmaceuticals in the aquatic environment. In this work, the mechanism and toxicity of DCF degradation by ClO2 under simulated water disinfection conditions were investigated. Experimental results indicate that rapid and significant oxidation of DCF occurred within the first few minutes; however, its mineralization process was longer than its degradation process. UPLC-MS and (1)H NMR spectroscopy were performed to identify major disinfection byproducts that were generated in three tentative degradation routes. The two main routes were based on initial decarboxylation of DCF on the aliphatic chain and hydroxylation of the phenylacetic acid moiety at the C-4 position. Subsequently, the formed aldehyde intermediates were the starting point for further multistep degradation involving decarboxylation, hydroxylation, and oxidation reactions of CN bond cleavage. The third route was based on transient preservation of chlorinated derivatives resulting from electrophilic attack by chlorine on the aromatic ring, which similarly underwent CN bond cleavage. Microtox bioassay was employed to evaluate the cytotoxicity of solutions treated by ClO2. The formation of more toxic mid-byproducts during the ClO2 disinfection process poses a potential risk to consumers.

  13. A Nanoarchitecture Based on Silver and Copper Oxide with an Exceptional Response in the Chlorine-Promoted Epoxidation of Ethylene.

    Science.gov (United States)

    Ramirez, Adrian; Hueso, Jose L; Suarez, Hugo; Mallada, Reyes; Ibarra, Alfonso; Irusta, Silvia; Santamaria, Jesus

    2016-09-01

    The selective oxidation of ethylene to ethylene epoxide is highly challenging as a result of competing reaction pathways leading to the deep oxidation of both ethylene and ethylene oxide. Herein we present a novel catalyst based on silver and copper oxide with an excellent response in the selective oxidation pathway towards ethylene epoxide. The catalyst is composed of different silver nanostructures dispersed on a tubular copper oxide matrix. This type of hybrid nanoarchitecture seems to facilitate the accommodation of chlorine promoters, leading to high yields at low reaction temperatures. The stability after the addition of chlorine promoters implies a substantial improvement over the industrial practice: a single pretreatment step at ambient pressure suffices in contrast with the common practice of continuously feeding organochlorinated precursors during the reaction.

  14. UV Irradiation Chlorine Dioxide Photocatalytic Oxidation of Simulated Fuchsine Wastewater by UV-Vis and Online FTIR Spectrophotometric Method

    OpenAIRE

    Jie Liu; Chunlei Huai; Na Li; Xiaomei Wang; Laishun Shi

    2012-01-01

    The photocatalyst TiO2/SiO2 was prepared and used for chlorine dioxide photocatalytic oxidation of simulated fuchsine wastewater under UV irradiation. The removal efficiency of fuchsine treated by photocatalytic oxidation process is higher than that of chemical oxidation process. By using UV-Vis and online FTIR analysis technique, the intermediates during the degradation process were obtained. The benzene ring in fuchsine was degraded into quinone and carboxylic acid and finally changed into ...

  15. Reduction of tri halomethanes in drinking water using chlorine dioxide as a pre oxidant; Rduccion de trihalometanos en agua potable mediante preoxidacion con dioxido de cloro

    Energy Technology Data Exchange (ETDEWEB)

    Marcian Cervera, V. J.; Monforte Monleon, L.; Ribera Orts, R.; Alvarez Alondiga, I.; Garcia Garrido, J.

    2007-07-01

    The object of the present study is to verify the suitability of using chlorine dioxide as a pre oxidant in the Water Treatment Plant of La Presa (Manises) and El Realon (Picassent), in order to minimize the tri halomethanes formation. To prove the effectiveness of chlorine dioxide, on the tri halomethanes precursors removal by oxidation, many controls and analytics have been done on the two water treatment plants. On the other hand this study also shows the chlorine dioxide generation method used, as well as its high disinfection efficiency, higher than the chlorine. (Author)

  16. STUDY OF THE EFFECT OF CHLORINE ADDITION ON MERCURY OXIDATION BY SCR CATALYST UNDER SIMULATED SUBBITUMINOUS COAL FLUE GAS

    Science.gov (United States)

    An entrained flow reactor is used to study the effect of addition of chlorine-containing species on the oxidation of elemental mercury (Hgo)by a selective catalytic reduction (SCR) catalyst in simulated subbituminous coal combustion flue gas. The combustion flue gas was doped wit...

  17. Increased formation of halomethanes during chlorination of chloramphenicol in drinking water by UV irradiation, persulfate oxidation, and combined UV/persulfate pre-treatments.

    Science.gov (United States)

    Wenhai, Chu; Tengfei, Chu; Erdeng, Du; Deng, Yang; Yingqing, Guo; Naiyun, Gao

    2016-02-01

    Ultraviolet/persulfate (UV/PS) has been widely used to generate sulfate radicals for degradation of water organic pollutants in previous studies. However, its impacts on disinfection byproduct formation during post-chlorination of degraded compounds is unclear. The objective of this study was to evaluate the impacts of UV irradiation, PS oxidation, and the combined UV/PS advanced oxidation process (AOP) pre-treatments on halomethane formation during the following chlorination of chloramphenicol (CAP), a model antibiotic commonly found in wastewater-impacted water. Results showed that CAP could be transformed to more trichloromethane (TCM) than monochloromethane (MCM) and dichloromethane (DCM) in the presence of excess chlorine. UV photolysis, PS oxidation and UV/PS AOP all directly decomposed CAP to produce halomethanes (HMs) before post-chlorination. Moreover, UV and UV/PS pre-treatments both enhanced the formation of all the HMs in the subsequent chlorination. PS pre-oxidation decreased the TCM formation during post-chlorination, but increased the yields of MCM, DCM and total HMs. UV pre-irradiation significantly increased the bromide utilization of HMs, whereas UV/PS pre-oxidation decreased the bromine incorporation and utilization of HMs from the chlorination of CAP in a low-bromide water. UV irradiation, PS oxidation, and UV/PS AOP can inactivate pathogens and degrade organic pollutants, but this benefit should be weighed against a potential risk of the increased halomethane formation from degraded organic pollutants with and without post-chlorination.

  18. Degradation kinetics of chlorinated aliphatic hydrocarbons by methane oxidizers naturally-associated with wetland plant roots.

    Science.gov (United States)

    Powell, C L; Goltz, M N; Agrawal, A

    2014-12-01

    Chlorinated aliphatic hydrocarbons (CAHs) are common groundwater contaminants that can be removed from the environment by natural attenuation processes. CAH biodegradation can occur in wetland environments by reductive dechlorination as well as oxidation pathways. In particular, CAH oxidation may occur in vegetated wetlands, by microorganisms that are naturally associated with the roots of wetland plants. The main objective of this study was to evaluate the cometabolic degradation kinetics of the CAHs, cis-1,2-dichloroethene (cisDCE), trichloroethene (TCE), and 1,1,1-trichloroethane (1,1,1TCA), by methane-oxidizing bacteria associated with the roots of a typical wetland plant in soil-free system. Laboratory microcosms with washed live roots investigated aerobic, cometabolic degradation of CAHs by the root-associated methane-oxidizing bacteria at initial aqueous [CH4] ~1.9mgL(-1), and initial aqueous [CAH] ~150μgL(-1); cisDCE and TCE (in the presence of 1,1,1TCA) degraded significantly, with a removal efficiency of approximately 90% and 46%, respectively. 1,1,1TCA degradation was not observed in the presence of active methane oxidizers. The pseudo first-order degradation rate-constants of TCE and cisDCE were 0.12±0.01 and 0.59±0.07d(-1), respectively, which are comparable to published values. However, their biomass-normalized degradation rate constants obtained in this study were significantly smaller than pure-culture studies, yet they were comparable to values reported for biofilm systems. The study suggests that CAH removal in wetland plant roots may be comparable to processes within biofilms. This has led us to speculate that the active biomass may be on the root surface as a biofilm. The cisDCE and TCE mass losses due to methane oxidizers in this study offer insight into the role of shallow, vegetated wetlands as an environmental sink for such xenobiotic compounds.

  19. Macrokinetic relationships between anodic processes in chlorine electrolysis on ruthenium-titanium oxide anodes

    International Nuclear Information System (INIS)

    Effect of porosity on kinetics of the main (chlorine evolution) and side (oxygen evolution and anodic dissolution of ruthenium dioxide) reactions for chlorine electrolysis conditions has been analyzed. Making allowance for chlorine hydrolysis secondary reaction, the distribution of chlorine concentration, solution pH and current densities of the main and side processes over the porous anode depth, have been found. It is shown that solution acidification in the anode pores due to chlorine hydrolysis can bring about replacement of oxygen evolution and ruthenium dioxide dissolution side reactions toward the porous anode external sides thus affecting its selectivity and corrosion resistance

  20. Quantification of chlorine in zirconium oxide and biological samples by instrumental NAA utilizing PCF of Dhruva reactor

    International Nuclear Information System (INIS)

    Recently studies on chlorine contents in various samples are being pursued due to its corrosive nature. Chlorine present at trace level in various finished products as well as powder is used as a raw material for production of different types of zircaloys used as structural materials in nuclear technology. As a part of quality assurance program, it is necessary to quantify chlorine accurately with suitable and simple technique. In the present work we have applied instrumental neutron activation analysis (INAA) utilizing its short-lived activation product (38Cl, 37 min, 1642 and 2168 keV) for its estimation. Pneumatic Carrier Facility (PCF) of Dhruva reactor, BARC was used sample irradiation of zirconium oxide dry powder, synthetic wax and IAEA RMs 1515 (Apple leaves) and Lichen 336. (author)

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

    KAUST Repository

    Liu, Chao

    2013-07-19

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

  2. Reactions of aqueous chlorine and chlorine dioxide with model food compounds.

    OpenAIRE

    Fukayama, M Y; Tan, H; Wheeler, W B; Wei, C I

    1986-01-01

    Chlorine and chlorine dioxide (ClO2), common disinfecting and bleaching chemicals used in the food industry, are potent oxidizing and chlorinating agents. Unfortunately, little is known about the nature of the reactions of chlorine with organic food constituents. This presentation reviews published information concerning the reactions of chlorine gas (Cl2[g]), aqueous chlorine, and ClO2 with model food compounds, the fate of chlorine during the chlorination of specific food products, and the ...

  3. Carbon isotope fractionation of chlorinated ethenes during oxidation by Fe{sup 2+} activated persulfate

    Energy Technology Data Exchange (ETDEWEB)

    Marchesi, Massimo, E-mail: m2marche@uwaterloo.ca [Departament de Cristallografia, Mineralogia i Diposits Minerals, Universitat de Barcelona, Barcelona, Catalunya 08028 (Spain); Earth and Environmental Department, University of Waterloo, Waterloo, Ontario, Canada N2L 3G1 (Canada); Aravena, Ramon [Earth and Environmental Department, University of Waterloo, Waterloo, Ontario, Canada N2L 3G1 (Canada); Sra, Kanwartej S. [Department of Civil and Environmental Engineering, University of Waterloo, Waterloo, Ontario, Canada N2L 3G1 (Canada); Golder Associates Inc, Toronto, Ontario, Canada L5N 5Z7 (Canada); Thomson, Neil R. [Department of Civil and Environmental Engineering, University of Waterloo, Waterloo, Ontario, Canada N2L 3G1 (Canada); Otero, Neus; Soler, Albert [Departament de Cristallografia, Mineralogia i Diposits Minerals, Universitat de Barcelona, Barcelona, Catalunya 08028 (Spain); Mancini, Silvia [Golder Associates Inc, Toronto, Ontario, Canada L5N 5Z7 (Canada)

    2012-09-01

    The increased use of persulfate (S{sub 2}O{sub 8}{sup 2-}) for in situ chemical oxidation to treat groundwater and soils contaminated by chlorinated hydrocarbon compounds (CHCs) requires unbiased methods to assess treatment performance. Stable carbon isotope analysis offers a potential tool for assessing the in situ treatment performance of persulfate at sites contaminated with CHCs. This study investigated the extent of C isotope fractionation during oxidation of tetrachloroethene (PCE), trichloroethene (TCE) and cis-dichloroethene (cis-DCE) by persulfate activated by ferrous ion (Fe{sup 2+}). An average carbon isotope enrichment factor {epsilon}{sub bulk} of - 4.9 Per-Mille-Sign for PCE, - 3.6 Per-Mille-Sign for TCE and - 7.6 Per-Mille-Sign for cis-DCE were obtained in batch experiments. Variations in the initial S{sub 2}O{sub 8}{sup 2-}/Fe{sup 2+}/CHC molar ratios did not result in any significant differences in carbon isotope fractionation. The occurrence of carbon isotope fractionation during oxidation and the lack of dependence of enrichment factors upon the S{sub 2}O{sub 8}{sup 2-}/Fe{sup 2+}/CHC molar ratio demonstrate that carbon isotope analysis can potentially be used at contaminated sites as an additional technique to estimate treatment efficacy during oxidation of CHCs by Fe{sup 2+} activated persulfate. Highlights: Black-Right-Pointing-Pointer The performance of in situ chemical oxidation (ISCO) is still difficult to assess. Black-Right-Pointing-Pointer We investigated the potential of carbon isotope analysis as a new assessing tool. Black-Right-Pointing-Pointer C isotope of PCE, TCE and DCE oxidized by persulfate activated by Fe{sup 2+} was measured. Black-Right-Pointing-Pointer Enrichment factors of - 4.9 Per-Mille-Sign for PCE, - 3.6 Per-Mille-Sign for TCE and - 7.6 Per-Mille-Sign for cisDCE were obtained. Black-Right-Pointing-Pointer Carbon isotope can potentially be used to estimate the ISCO treatment efficacy.

  4. Chlorine-doped reduced graphene oxide nanosheets as an efficient and stable electrode for supercapacitor in acidic medium.

    Science.gov (United States)

    Kakaei, Karim; Hamidi, Milad; Husseindoost, Somayeh

    2016-10-01

    We demonstrate the efficient doping of reduced graphene oxide (RGO) by Chlorine and its capacitive performance was calculated by cyclic voltammetry and charge-discharge cycling in 1M H2SO4 solution. In this regard, we are prepared RGO nanosheets through a simple, eco-friendly and efficient electrochemical method, with selectively functionalized edges by chlorine which involves added the RGO to the halogen-containing acid solution and dispersed by ultrasonic. After synthesis, Cl-RGO is characterized using X-ray diffraction, Raman spectroscopy, Fourier-transform infrared (FTIR) spectroscopy, Energy-dispersive X-ray (EDX) spectroscopy and tunneling electron microscopy. FTIR spectra show the chlorine-containing functional groups. Energy-dispersive X-ray spectroscopy analysis confirmed the presence of doped chlorine in RGO. Raman spectroscopy shows a high density of defects in the RGO layer. Electrochemical characteristics of Cl-RGO are characterized by cyclic voltammetery, galvanostatic charge/discharge and electrochemical impedance spectroscopy. According to the galvanostatic charge/discharge analysis, Cl-RGO represents specific capacitance (Cs) of 178.4Fg(-1) at current density of 1Ag(-1), which is higher than that of RGO (100.5Fg(-1)) in H2SO4 solution. PMID:27388125

  5. Oxidation of diclofenac with chlorine dioxide in aquatic environments: influences of different nitrogenous species.

    Science.gov (United States)

    Wang, Yingling; Liu, Haijin; Liu, Guoguang; Xie, Youhai; Ni, Tianjun

    2015-06-01

    The oxidation of diclofenac (DCF), a non-steroidal anti-inflammatory drug and emerging water pollutant, with chlorine dioxide was investigated under simulated water disinfection conditions. The reaction kinetics as functions of the initial concentrations of DCF, different nitrogenous species, and different pE values were experimentally determined. The results demonstrated that DCF reacted rapidly with ClO2, where more than 75 % of DCF (≤3.00 μM) was removed by 18.94 μM ClO2 within 60 s. All of the reactions followed pseudo first-order kinetics with respect to DCF, and the rate constant, k obs, exhibited a significant decrease from 4.21 × 10(-2) to 8.09 × 10(-3) s(-1), as the initial DCF concentration was increased from 1.00 to 5.00 μM. Furthermore, the degradation kinetics of DCF was clearly dependent on nitrogen-containing ion concentrations in the reaction solution. Ammonium and nitrite ions inhibited the DCF degradation by ClO2, whereas nitrate ion clearly initiated its promotion. In contrast, the inhibitory effect of NO2 (-) was more robust than that of NH4 (+). When the values of pE were gradually increased, the transformation of NH4 (+) to NO2 (-), and subsequently to NO3 (-), would occur, the rate constants were initially decreased, and then increased. When NH4 (+) and NO2 (-) coexisted, the inhibitory effect on the DCF degradation was less than the sum of the partial inhibitory effect. However, when NO2 (-) and NO3 (-) coexisted, the actual inhibition rate was greater than the theoretical estimate. These results indicated that the interaction of NH4 (+) and NO2 (-) was antagonistic, while the coexistence of NO2 (-) and NO3 (-) was observed to have a synergistic effect in aqueous environments. PMID:25604564

  6. Fabrication and Characterization of a SPR Based Fiber Optic Sensor for the Detection of Chlorine Gas Using Silver and Zinc Oxide

    Directory of Open Access Journals (Sweden)

    Sruthi P. Usha

    2015-04-01

    Full Text Available A fiber optic chlorine gas sensor working on surface plasmon resonance (SPR technique fabricated using coatings of silver and zinc oxide films over unclad core of the optical fiber is reported. The sensor probe is characterized using wavelength interrogation and recording SPR spectra for different concentrations of chlorine gas around the probe. A red shift is observed in the resonance wavelength on increasing the concentration of the chlorine gas. The thickness of the zinc oxide film is optimized to achieve the maximum sensitivity of the sensor. In addition to wavelength interrogation, the sensor can also work on intensity modulation. The selectivity of the sensor towards chlorine gas is verified by carrying out measurements for different gases. The sensor has various advantages such as better sensitivity, good selectivity, reusability, fast response, low cost, capability of online monitoring and remote sensing.

  7. Application of in situ chemical oxidation technique with potassium permanganate for the remediation of a shallow aquifer contaminated with chlorinated solvents

    OpenAIRE

    Alaine Santos da Cunha; Reginaldo Antonio Bertolo

    2012-01-01

    In situ chemical oxidation is a method that is frequently being used for the remediation of contaminated areas, since it presents an adequate efficiency in the reduction of the contaminant mass, particularly chlorinated ethenes, in a relatively short period of time. This manuscript presents the results of the application of this method, using the injection of potassium permanganate as the remediation agent, in an impacted area with chlorinated organic compounds, especially 1,1-dichloroethene....

  8. Effect of chlorination and ozone pre-oxidation on the photobacteria acute toxicity for dissolved organic matter from sewage treatment plants

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    The effect of chlorination and ozone pre-oxidation on the photobacteria acute toxicity for dissolved organic matter(DOM) from sewage treatment plants was investigated in this study.The results show that ozone pre-oxidation enhanced the photobacteria acute toxicity of the water samples.DOM before and after ozone pre-oxidation was fractionated by resins into six kinds of hydrophobic and hydrophilic organics.The six fractions were chlorinated individually and the photobacteria acute toxicity before and after chlorination was tested.It was found that the percentage of hydrophilic organics in DOM significantly increased after ozone pre-oxidation and hydrophilic organics exhibited remarkably higher acute toxicity than hydrophobic organics.In view of potentiometric titration and fourier transform infrared(FTIR) analysis,the hydrophilic organics showed a rather higher content of ph-OH structures than hydrophobic organics.

  9. Surface water disinfection by chlorination and advanced oxidation processes: Inactivation of an antibiotic resistant E. coli strain and cytotoxicity evaluation.

    Science.gov (United States)

    Miranda, Andreza Costa; Lepretti, Marilena; Rizzo, Luigi; Caputo, Ivana; Vaiano, Vincenzo; Sacco, Olga; Lopes, Wilton Silva; Sannino, Diana

    2016-06-01

    The release of antibiotics into the environment can result in antibiotic resistance (AR) spread, which in turn can seriously affect human health. Antibiotic resistant bacteria have been detected in different aquatic environments used as drinking water source. Water disinfection may be a possible solution to minimize AR spread but conventional processes, such as chlorination, result in the formation of dangerous disinfection by-products. In this study advanced oxidation processes (AOPs), namely H2O2/UV, TiO2/UV and N-TiO2/UV, have been compared with chlorination in the inactivation of an AR Escherichia coli (E. coli) strain in surface water. TiO2 P25 and nitrogen doped TiO2 (N-TiO2), prepared by sol-gel method at two different synthesis temperatures (0 and -20°C), were investigated in heterogeneous photocatalysis experiments. Under the investigated conditions, chlorination (1.0mgL(-1)) was the faster process (2.5min) to achieve total inactivation (6 Log). Among AOPs, H2O2/UV resulted in the best inactivation rate: total inactivation (6 Log) was achieved in 45min treatment. Total inactivation was not observed (4.5 Log), also after 120min treatment, only for N-doped TiO2 synthesized at 0°C. Moreover, H2O2/UV and chlorination processes were evaluated in terms of cytotoxicity potential by means of 3-(4,5-dime-thylthiazol-2-yl)-2,5-diphenylte-trazolium colorimetric test on a human-derived cell line and they similarly affected HepG2 cells viability. PMID:26945469

  10. Surface water disinfection by chlorination and advanced oxidation processes: Inactivation of an antibiotic resistant E. coli strain and cytotoxicity evaluation.

    Science.gov (United States)

    Miranda, Andreza Costa; Lepretti, Marilena; Rizzo, Luigi; Caputo, Ivana; Vaiano, Vincenzo; Sacco, Olga; Lopes, Wilton Silva; Sannino, Diana

    2016-06-01

    The release of antibiotics into the environment can result in antibiotic resistance (AR) spread, which in turn can seriously affect human health. Antibiotic resistant bacteria have been detected in different aquatic environments used as drinking water source. Water disinfection may be a possible solution to minimize AR spread but conventional processes, such as chlorination, result in the formation of dangerous disinfection by-products. In this study advanced oxidation processes (AOPs), namely H2O2/UV, TiO2/UV and N-TiO2/UV, have been compared with chlorination in the inactivation of an AR Escherichia coli (E. coli) strain in surface water. TiO2 P25 and nitrogen doped TiO2 (N-TiO2), prepared by sol-gel method at two different synthesis temperatures (0 and -20°C), were investigated in heterogeneous photocatalysis experiments. Under the investigated conditions, chlorination (1.0 mg L(-1)) was the faster process (2.5 min) to achieve total inactivation (6 Log). Among AOPs, H2O2/UV resulted in the best inactivation rate: total inactivation (6 Log) was achieved in 45 min treatment. Total inactivation was not observed (4.5 Log), also after 120 min treatment, only for N-doped TiO2 synthesized at 0°C. Moreover, H2O2/UV and chlorination processes were evaluated in terms of cytotoxicity potential by means of 3-(4,5-dime-thylthiazol-2-yl)-2,5-diphenylte-trazolium colorimetric test on a human-derived cell line and they similarly affected HepG2 cells viability.

  11. Insight into the unique oxidation chemistry of elemental mercury by chlorine-containing species: experiment and simulation.

    Science.gov (United States)

    Byun, Youngchul; Cho, Moohyun; Namkung, Won; Lee, Kiman; Koh, Dong Jun; Shin, Dong Nam

    2010-03-01

    This work investigated the oxidation chemistry of elemental mercury (Hg(0)) by chlorine-containing species produced indirectly through the gas-to-solid phase reaction between NO(x) gases and NaClO(2) powder (NaClO(2)(s)), where both experiment and simulation results were compared to clarify which species are responsible for the oxidation of Hg(0). At first, we introduced 30 ppm of NO(2) into the pack-bed reactor containing NaClO(2)(s) to produce OClO species and then injected NO and Hg(0) (260 microg/Nm(3)) to Mixer, where the concentration of NO was varied up to 180 ppm and the reaction temperature was set to 130 degrees C. We observed for the first time that the degree of Hg(0) oxidation is completely controlled by the introduced concentration of NO: for example, the oxidation efficiency of Hg(0) is drastically increased to become 100% at near 7 ppm NO, but further increasing NO concentration results in the oxidation efficiency of Hg(0) being gradually decreased. The simulation results indicated that such a propensity of Hg(0) oxidation efficiency to NO concentration can be attributed to the NO concentration-dependent Cl, ClO, and Cl(2) formation which plays a critical role in the oxidation of Hg(0). PMID:20131790

  12. 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.

  13. Oxidation of MC-LR and -RR with chlorine and potassium permanganate: toxicity of the reaction products.

    Science.gov (United States)

    Rodríguez, Eva M; Acero, Juan L; Spoof, Lisa; Meriluoto, Jussi

    2008-03-01

    Toxin-producing cyanobacteria are abundant in surface waters used as drinking water resources. Microcystins (MC) produced by certain cyanobacteria present acute and chronic toxicity, and their removal in drinking water treatment processes is of increasing concern. Previous studies have demonstrated that chlorine and potassium permanganate are feasible oxidants for the removal of MCs present in drinking water resources, although the oxidation might lead to toxic oxidation products. In this paper, the toxicity of the oxidation products of MC-LR and -RR has been studied using protein phosphatase 1 inhibition assay (PPIA). The HPLC and ELISA analyses correlated with the PPIA results for both toxins. The samples containing the oxidation products were fractionated by HPLC and the toxicity of the fractions was tested with PPIA. The results revealed that protein phosphatase 1 inhibition emerged only from intact MC, while the oxidation products were non-toxic. Similar results were obtained in experiments performed in natural waters: no reaction products or interactions exhibiting protein phosphatase 1 inhibition were detected.

  14. Reaction of bromine and chlorine with phenolic compounds and natural organic matter extracts--Electrophilic aromatic substitution and oxidation.

    Science.gov (United States)

    Criquet, Justine; Rodriguez, Eva M; Allard, Sebastien; Wellauer, Sven; Salhi, Elisabeth; Joll, Cynthia A; von Gunten, Urs

    2015-11-15

    Phenolic compounds are known structural moieties of natural organic matter (NOM), and their reactivity is a key parameter for understanding the reactivity of NOM and the disinfection by-product formation during oxidative water treatment. In this study, species-specific and/or apparent second order rate constants and mechanisms for the reactions of bromine and chlorine have been determined for various phenolic compounds (phenol, resorcinol, catechol, hydroquinone, phloroglucinol, bisphenol A, p-hydroxybenzoic acid, gallic acid, hesperetin and tannic acid) and flavone. The reactivity of bromine with phenolic compounds is very high, with apparent second order rate constants at pH 7 in the range of 10(4) to 10(7) M(-1) s(-1). The highest value was recorded for the reaction between HOBr and the fully deprotonated resorcinol (k = 2.1 × 10(9) M(-1) s(-1)). The reactivity of phenolic compounds is enhanced by the activating character of the phenolic substituents, e.g. further hydroxyl groups. With the data set from this study, the ratio between the species-specific rate constants for the reactions of chlorine versus bromine with phenolic compounds was confirmed to be about 3000. Phenolic compounds react with bromine or chlorine either by oxidation (electron transfer, ET) or electrophilic aromatic substitution (EAS) processes. The dominant process mainly depends on the relative position of the hydroxyl substituents and the possibility of quinone formation. While phenol, p-hydroxybenzoic acid and bisphenol A undergo EAS, hydroquinone, catechol, gallic acid and tannic acid, with hydroxyl substituents in ortho or para positions, react with bromine by ET leading to quantitative formation of the corresponding quinones. Some compounds (e.g. phloroglucinol) show both partial oxidation and partial electrophilic aromatic substitution and the ratio observed for the pathways depends on the pH. For the reaction of six NOM extracts with bromine, electrophilic aromatic substitution

  15. Comparisons of the film peeling from the composite oxides of quartz sand filters using ozone, hydrogen peroxide and chlorine dioxide.

    Science.gov (United States)

    Guo, Yingming; Huang, Tinglin; Wen, Gang; Cao, Xin

    2015-08-01

    To solve the problem of shortened backwashing intervals in groundwater plants, several disinfectants including ozone (O3), hydrogen peroxide (H2O2) and chlorine dioxide (ClO2) were examined to peel off the film from the quartz sand surface in four pilot-scale columns. An optimized oxidant dosage and oxidation time were determined by batch tests. Subsequently, the optimized conditions were tested in the four pilot-scale columns. The results demonstrated that the backwashing intervals increased from 35.17 to 54.33 (H2O2) and to 53.67 hr (ClO2) after the oxidation treatments, and the increase of backwashing interval after treatment by O3 was much less than for the other two treatments. Interestingly, the treatment efficiency of filters was not affected by O3 or H2O2 oxidation; but after oxidation by ClO2, the treatment efficiency was deteriorated, especially the ammonia removal (from 96.96% to 24.95%). The filter sands before and after the oxidation were characterized by scanning electron microscopy and X-ray photoelectron spectroscopy. Compared with the oxidation by O3 and H2O2, the structures on the surface of filter sands were seriously damaged after oxidation by ClO2. The chemical states of manganese on the surfaces of those treated sands were only changed by ClO2. The damage of the structures and the change of the chemical states of manganese might have a negative effect on the ammonia removal. In summary, H2O2 is a suitable agent for film peeling. PMID:26257342

  16. Alleviation of membrane fouling in a submerged membrane bioreactor with electrochemical oxidation mediated by in-situ free chlorine generation.

    Science.gov (United States)

    Chung, Chong Min; Tobino, Tomohiro; Cho, Kangwoo; Yamamoto, Kazuo

    2016-06-01

    The control of membrane fouling is still the biggest challenge that membrane bioreactor (MBR) for wastewater treatment faces with. In this report, we evince that an in-situ electrochemical free chlorine generation is effective for membrane fouling mitigation. An electrochemical oxidation (EO) apparatus with perforated Ti/IrO2 anodes and Ti/Pt cathodes was integrated into a conventional MBR with microfiltration module (EO-MBR). The membrane fouling characteristics of EO-MBR fed with synthetic wastewater were monitored for about 2 months in comparison to control MBRs. In the EO-MBR at a direct current density of 0.4 mA/cm(2), the frequency of membrane fouling when the trans-membrane pressure (TMP) reached 30 kPa was effectively reduced by 40% under a physical membrane cleaning regime. The evolution patterns of TMP together with hydraulic resistance analysis based on resistance-in-series model indicated that the electrochemically generated active chlorine alleviated the physically irremovable membrane fouling. Further analysis on extracellular polymeric substances (EPS) of sludge cake layer (SCL) revealed significant reductions of protein contents in soluble EPS and fluorescence emission intensities from humic acids and other fluorophores in bound EPS, which in-turn would decrease the hydrophobic accumulation of organic foulants on membrane pores. The chlorine dosage from the EO apparatus was estimated to be 4.7 mg Cl2/g MLVSS/day and the overall physicochemical properties (bio-solids concentration, floc diameter, zeta-potential) as well as the microbial activity in terms of specific oxygen utilization rate and removal efficiency of dissolved organic carbon (>97%) were not affected significantly. A T-RFLP (terminal restriction fragment length polymorphism) analysis suggested noticeable shifts in microbial community both in mixed liquor and sludge cake layer. Consequently, our electrochemical chlorination would be an efficient fouling control strategy in membrane

  17. IN-SITU DUOX™ CHEMICAL OXIDATION TECHNOLOGY TO TREAT CHLORINATED ORGANICS AT THE ROOSEVELT MILLS SITE, VERNON, CT: SITE CHARACTERIZATION AND TREATABILITY STUDY

    Science.gov (United States)

    A study was performed investigating the feasibility of applying the DUOX™ chemical oxidation technology to chlorinated solvent contaminated media at the Roosevelt Mills site in Vernon, Connecticut. The Roosevelt Mills site is a former woolen mill that included dry cleaning operat...

  18. Inductively coupled plasma torch efficiency at atmospheric pressure for organo-chlorine liquid waste removal: Chloroform destruction in oxidative conditions

    Energy Technology Data Exchange (ETDEWEB)

    Kamgang-Youbi, Georges, E-mail: kamyougeo@yahoo.fr [French Atomic Commission-CEA, Marcoule-DTCD/SCDV/LPIC, BP 17171, 30207 Bagnols-Sur-Cèze Cedex (France); Department of Inorganic Chemistry, The University of Yaounde I, P.O Box, 812 Yaounde (Cameroon); Poizot, Karine; Lemont, Florent [French Atomic Commission-CEA, Marcoule-DTCD/SCDV/LPIC, BP 17171, 30207 Bagnols-Sur-Cèze Cedex (France)

    2013-01-15

    Highlights: ► Inductively plasma torch is used for the decomposition of organochlorine molecule. ► We examine the impact of liquid water substitution by oxygen gas as oxidant. ► Complete and safe decomposition is achieved with the presence of oxygen. ► The energy efficiency and capabilities of process are better with O{sub 2} than H{sub 2}O. -- Abstract: The performance of a plasma reactor for the degradation of chlorinated hydrocarbon waste is reported. Chloroform was used as a target for a recently patented destruction process based using an inductive plasma torch. Liquid waste was directly injected axially into the argon plasma with a supplied power of ∼4 kW in the presence of oxygen as oxidant and carrier gas. Decomposition was performed at CHCl{sub 3} feed rates up to 400 g h{sup −1} with different oxygen/waste molar ratios, chloroform destruction was obtained with at least 99% efficiency and the energy efficiency reached 100 g kWh{sup −1}. The conversion end products were identified and assayed by online FTIR spectroscopy (CO{sub 2}, HCl and H{sub 2}O) and redox titration (Cl{sub 2}). Considering phosgene as representative of toxic compounds, only very small quantities of toxics were released (<1 g h{sup −1}) even with high waste feed rates. The experimental results were very close to the equilibrium composition predicted by thermodynamic calculations. At the bottom of the reactor, the chlorinated acids were successfully trapped in a scrubber and transformed into mineral salts, hence, only CO{sub 2} and H{sub 2}O have been found in the final off-gases composition.

  19. Kinetics and Mechanisms of Cr(VI) Formation via the Oxidation of Cr(III) Solid Phases by Chlorine in Drinking Water.

    Science.gov (United States)

    Chebeir, Michelle; Liu, Haizhou

    2016-01-19

    Hexavalent chromium Cr(VI), typically existing as the oxyanion form of CrO4(2-), is being considered for more stringent drinking water standards by regulatory agencies. Cr(VI) can be inadvertently produced via the oxidation of trivalent chromium Cr(III) solids. This study investigated the kinetics and mechanisms of Cr(III) solids oxidation by chlorine in drinking water and associated Cr(VI) formation. Batch experiments were carried out with three Cr(III) solids of environmental relevance, i.e., chromium hydroxide Cr(OH)3(s), chromium oxide Cr2O3(s), and copper chromite Cu2Cr2O5(s). Impacts of water chemical parameters including pH (6.0-8.5) and bromide concentration (0-5 mg/L) were examined. Results showed that the rapid oxidation of Cr(III) solid phases by chlorine was accompanied by Cr(VI) formation and an unexpected production of dissolved oxygen. Analysis of reaction stoichiometry indicated the existence of Cr intermediate species that promoted the autocatalytic decay of chlorine. An increase in pH modestly enhanced Cr(VI) formation due to changes of reactive Cr(III) surface hydroxo species. Bromide, a trace chemical constituent in source waters, exhibited a catalytic effect on Cr(VI) formation due to an electron shuttle mechanism between Cr(III) and chlorine and the bypass of Cr intermediate formation. The kinetics data obtained from this study suggest that the oxidation of Cr(III) solids by chlorine in water distribution systems can contribute to Cr(VI) occurrence in tap water, especially in the presence of a trace level of bromide.

  20. Zirconia concentrate chlorination

    International Nuclear Information System (INIS)

    Chlorination experiments were conducted in order to study the kinetics of gasification of the zirconium oxide present in the zirconia concentrate. The variables studied are temperature (1173 to 1373 K), percentage of reducing agent (12 to 36%) and porosity (22 to 30%). The results indicated a greater influence of temperature and percentage of reducing agent as well as allowed the conclusion that a balance between the levels of these variables is an important factor in the appropriate chlorination conditions. (author)

  1. Development and Electrochemical Studies of Ruthenium Based Mixed Oxide Catalyst Electrodes for Chlorine Evolution

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Experimental results are presented which allow comparison of the electrochemical performance of RuO2/Ti, Ru0.3Sn0.7O2/Ti and Ru0.3V0.7O2/Ti catalysts prepared on a titanium substrate by thermal decomposition from respective precursors. The highest activity for chlorine evolution is observed on the Ru0.3V0.7O2/Ti electrode, lower on Ru0.3Sn0.7O2/Ti and least on RuO2/Ti. Voltammograms obtained in the polarisable region are used to characterize the different electrodes. Further more an analysis of the catalytic activity and reaction kinetics of the developed electrodes in NaCl are presented.

  2. Efficient oxidative dechlorination and aromatic ring cleavage of chlorinated phenols catalyzed by iron sulfophthalocyanine

    Energy Technology Data Exchange (ETDEWEB)

    Sorokin, A.; Meunier, B. [Laboratoire de Chimie de Coordination du CNRS, Toulouse (France); Seris, J.L. [Elf-Aquitaine, Artix (France)

    1995-05-26

    An efficient method has been developed for the catalytic oxidation of pollutants that are not easily degraded. The products of the hydrogen peroxide (H{sub 2}O{sub 2}) oxidation of 2,4,6-trichlorophenol (TCP) catalyzed by the iron complex 2,9,16,23-tetrasulfophthalocyanine (FePcS) were observed to be chloromaleic, chlorofumaric, maleic, and fumaric acids from dechlorination and aromatic cycle cleavage, as well as additional products that resulted from oxidative coupling. Quantitative analysis of the TCP oxidation reaction revealed that up to two chloride ions were released per TCP molecule. This chemical system, consisting of an environmentally safe oxidant (H{sub 2}O{sub 2}) and an easily accessible catalyst (FePcS), can perform several key steps in the oxidative mineralization of TCP, a paradigm of recalcitrant pollutants. 20 refs., 4 figs., 2 tabs.

  3. Microbial dynamics during and after in situ chemical oxidation of chlorinated solvents

    NARCIS (Netherlands)

    Sutton, N.B.; Atashgahi, S.; Wal, van der J.; Wijn, G.; Grotenhuis, J.T.C.; Smidt, H.; Rijnaarts, H.

    2015-01-01

    In situ chemical oxidation (ISCO) followed by a bioremediation step is increasingly being considered as an effective biphasic technology. Information on the impact of chemical oxidants on organohalide respiring bacteria (OHRB), however, is largely lacking. Therefore, we used quantitative PCR (qPCR)

  4. Reactivity of selenium-containing compounds with myeloperoxidase-derived chlorinating oxidants

    DEFF Research Database (Denmark)

    Carroll, Luke; Pattison, David I.; Fu, Shanlin;

    2015-01-01

    and N-chloramines, causes damage to host tissue. Low molecular mass thiol compounds, including glutathione (GSH) and methionine (Met), have demonstrated efficacy in scavenging MPO-derived oxidants, which prevents oxidative damage in vitro and ex vivo. Selenium species typically have greater reactivity...... toward oxidants compared to the analogous sulfur compounds, and are known to be efficient scavengers of HOCl and other hypohalous acids produced by MPO. In this study, we examined the efficacy of a number of sulfur and selenium compounds to scavenge a range of biologically relevant N-chloramines and...... oxidants produced by both isolated MPO and activated neutrophils and characterized the resulting selenium-derived oxidation products in each case. A dose-dependent decrease in the concentration of each N-chloramine was observed on addition of the sulfur compounds (cysteine, methionine) and selenium...

  5. Three-dimensional density-dependent flow and multicomponent reactive transport modeling of chlorinated solvent oxidation by potassium permanganate

    Science.gov (United States)

    Henderson, Thomas H.; Mayer, K. Ulrich; Parker, Beth L.; Al, Tom A.

    2009-05-01

    A popular method for the treatment of aquifers contaminated with chlorinated solvents is chemical oxidation based on the injection of potassium permanganate (KMnO 4). Both the high density (1025 gL - 1 ) and reactivity of the treatment solution influence the fate of permanganate (MnO 4) in the subsurface and affect the degree of contaminant treatment. The MIN3P multicomponent reactive transport code was enhanced to simulate permanganate-based remediation, to evaluate the pathways of MnO 4 utilization, and to assess the role of density contrasts for the delivery of the treatment solution. The modified code (MIN3P-D) provides a direct coupling between density-dependent fluid flow, solute transport, contaminant treatment, and geochemical reactions. The model is used to simulate a field trial of TCE oxidation in a sandy aquifer that is underlain by an aquitard. Three-dimensional simulations are conducted for a coupled reactive system comprised of ten aqueous components, two mineral phases, TCE (dissolved, adsorbed, and NAPL), reactive organic matter, and including ion exchange reactions. Model parameters are constrained by literature data and a detailed data set from the field site under investigation. The general spatial and transient evolution in observed concentrations of the oxidant, dissolved TCE, and reaction products are adequately reproduced by the simulations. The model elucidates the important role of density-induced flow and transport on the distribution of the treatment solution into NAPL containing regions located at the aquifer-aquitard interface. Model results further suggest that reactions that do not directly affect the stability of MnO 4 have a negligible effect on solution density and MnO 4 delivery.

  6. Chlorination of UO2, PuO2 and rare earth oxides using ZrCl4 in LiCl-KCl eutectic melt

    International Nuclear Information System (INIS)

    A new chlorination method using ZrCl4 in a molten salt bath has been investigated for the pyrometallurgical reprocessing of nuclear fuels. ZrCl4 has a high reactivity with oxygen but is not corrosive to refractory metals such as steel. Rare earth oxides (La2O3, CeO2, Nd2O3 and Y2O3) and actinide oxides (UO2 and PuO2) were allowed to react with ZrCl4 in a LiCl-KCl eutectic salt at 773 K to give a metal chloride solution and a precipitate of ZrO2. An addition of zirconium metal as a reductant was effective in chlorinating the dioxides. When the oxides were in powder form, the reaction was observed to progress rapidly. Cyclic voltammetry provided a convenient way of establishing when the reaction was completed. It was demonstrated that the ZrCl4 chlorination method, free from corrosive gas, was very simple and useful

  7. Enhanced photocatalytic activity of degrading short chain chlorinated paraffins over reduced graphene oxide/CoFe2O4/Ag nanocomposite.

    Science.gov (United States)

    Chen, Xin; Zhao, Qidong; Li, Xinyong; Wang, Dong

    2016-10-01

    Short chain chlorinated paraffins have recently attracted great attention because of their environmental persistence and biological toxicity as an important organic pollutant. In this work, reduced graphene oxide/CoFe2O4/Ag (RGO/CoFe2O4/Ag) nanocomposite was prepared and employed for photocatalytic degradation of short chain chlorinated paraffins. The process of photocatalytic degradation of short chain chlorinated paraffins over RGO/CoFe2O4/Ag under visible light (λ>400nm) was investigated by in situ Fourier transform infrared spectroscopy and the related mechanisms were proposed. An apparent degradation ratio of 91.9% over RGO/CoFe2O4/Ag could be obtained under visible light illumination of 12h, while only about 21.7% was obtained with commercial P25 TiO2 under the same experimental conditions, which demonstrates that the RGO/CoFe2O4/Ag nanocomposite is a potential candidate for effective photocatalytic removal of short chain chlorinated paraffins. PMID:27376973

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

    OpenAIRE

    Ferreira, Francisco Cardoso

    1991-01-01

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

  9. Oxidation of elemental mercury by chlorine: Gas phase, Surface, and Photo-induced reaction pathways

    OpenAIRE

    Yan, Nai-Qiang; Liu, Shou-Heng; Chang, Shih-Ger

    2004-01-01

    Accurate oxidation rate constants of mercury gas are needed for determining its dispersion and lifetime in the atmosphere. They would also help in developing a technology for the control of mercury emissions from coal-fired power plants. However, it is difficult to establish the accurate rate constants primarily due to the fact that mercury easily adsorbs on solid surface and its reactions can be catalyzed by the surface. We have demonstrated a procedure that allows the determination of ...

  10. Citric Acid-Modified Fenton's Reaction for the Oxidation of Chlorinated Ethylenes in Soil Solution Systems

    Energy Technology Data Exchange (ETDEWEB)

    Seol, Yongkoo; Javandel, Iraj

    2008-03-15

    Fenton's reagent, a solution of hydrogen peroxide and ferrous iron catalyst, is used for an in-situ chemical oxidation of organic contaminants. Sulfuric acid is commonly used to create an acidic condition needed for catalytic oxidation. Fenton's reaction often involves pressure buildup and precipitation of reaction products, which can cause safety hazards and diminish efficiency. We selected citric acid, a food-grade substance, as an acidifying agent to evaluate its efficiencies for organic contaminant removal in Fenton's reaction, and examined the impacts of using citric acid on the unwanted reaction products. A series of batch and column experiments were performed with varying H{sub 2}O{sub 2} concentrations to decompose selected chlorinated ethylenes. Either dissolved iron from soil or iron sulfate salt was added to provide the iron catalyst in the batch tests. Batch experiments revealed that both citric and sulfuric acid systems achieved over 90% contaminant removal rates, and the presence of iron catalyst was essential for effective decontamination. Batch tests with citric acid showed no signs of pressure accumulation and solid precipitations, however the results suggested that an excessive usage of H{sub 2}O{sub 2} relative to iron catalysts (Fe{sup 2+}/H{sub 2}O{sub 2} < 1/330) would result in lowering the efficiency of contaminant removal by iron chelations in the citric acid system. Column tests confirmed that citric acid could provide suitable acidic conditions to achieve higher than 55% contaminant removal rates.

  11. Oxidizing behavior of some platinum metal fluorides. [Xe complexes with Pt, Pd fluorides; Chlorine-2 oxidation by transition metal hexafluorides

    Energy Technology Data Exchange (ETDEWEB)

    Graham, L.

    1978-10-01

    The previously known compounds Xe/sub 2/F/sub 3//sup +/PtF/sub 6//sup -/, XeF/sup +/PtF/sub 6//sup -/ and XeF/sub 2/.2PtF/sub 4/(XePt/sub 2/F/sub 10/) were prepared by the interaction of XeF/sub 2/ with PtF/sub 4/. The new compounds XeF/sub 2/.PdF/sub 4/ and XeF/sub 2/.2PdF/sub 4/(XePd/sub 2/F/sub 10/) were produced by interaction of XeF/sub 2/ with either PdF/sub 4/ or Pd/sub 2/F/sub 6/. A weight loss-versus-time curve indicated the presence of 4:1, 3:1 and 2:1 XeF/sub 2//PdF/sub 4/ complexes. The thermal decomposition of XeFPtF/sub 6/ or XePd/sub 2/F/sub 10/ yields highly pure XeF/sub 4/. Thus the interaction of XeF/sub 2/ with platinum fluorides (PtF/sub 4/ or PtF/sub 5/) or palladium fluorides (Pd/sub 2/F/sub 6/ or PdF/sub 4/) provides for the conversion of XeF/sub 2/ to XeF/sub 4/. The compound XePd/sub 2/F/sub 10/ is a close structural relative of XePt/sub 2/F/sub 10/, and spectroscopic evidence suggests that both are salts of XeF/sup +/ and a polymeric (M/sub 2/F/sub 9/)/sub x//sup x-/ ion. A Xe:PtF/sub 6/ material of approximately 1:1 stoichiometry has been prepared and compared with XePdF/sub 6/(XeF/sub 2/.PdF/sub 4/). The interaction of chlorine with the third-series transition metal hexafluorides has been investigated. Gravimetric and tensimetric evidence indicate that the initial product of the Cl/sub 2/ plus IrF/sub 6/ reaction is a solid of composition Cl/sub 2/IrF/sub 6/. Vibrational spectroscopic and other evidence indicates that this solid yields a sequence of products, of which Cl/sub 3//sup +/IrF/sub 6//sup -/, Cl/sub 3//sup +/Ir/sub 2/F/sub 11//sup -/ and Ir/sub 4/F/sub 20/ have been identified, the last being the ultimate solid product of the room temperature decomposition of the adduct. A new chlorine fluoride generated in the room temperature decomposition of Cl/sub 2/IrF/sub 6/ has been tentatively formulated as Cl/sub 3/F from infrared evidence.

  12. Oxidative stress induced by chlorine dioxide as an insecticidal factor to the Indian meal moth, Plodia interpunctella.

    Science.gov (United States)

    Kumar, Sunil; Park, Jiyeong; Kim, Eunseong; Na, Jahyun; Chun, Yong Shik; Kwon, Hyeok; Kim, Wook; Kim, Yonggyun

    2015-10-01

    A novel fumigant, chlorine dioxide (ClO2) is a commercial bleaching and disinfection agent. Recent study indicates its insecticidal activity. However, its mode of action to kill insects is yet to be understood. This study set up a hypothesis that an oxidative stress induced by ClO2 is a main factor to kill insects. The Indian meal moth, Plodia interpunctella, is a lepidopteran insect pest infesting various stored grains. Larvae of P. interpunctella were highly susceptible to ClO2 gas, which exhibited an acute toxicity. Physiological damages by ClO2 were observed in hemocytes. At high doses, the larvae of P. interpunctella suffered significant reduction of total hemocytes. At low doses, ClO2 impaired hemocyte behaviors. The cytotoxicity of ClO2 was further analyzed using two insect cell lines, where Sf9 cells were more susceptible to ClO2 than High Five cells. The cells treated with ClO2 produced reactive oxygen species (ROS). The produced ROS amounts increased with an increase of the treated ClO2 amount. However, the addition of an antioxidant, vitamin E, significantly attenuated the cytotoxicity of ClO2 in a dose-dependent manner. To support the oxidative stress induced by ClO2, two antioxidant genes (superoxide dismutase (SOD) and thioredoxin-peroxidase (Tpx)) were identified from P. interpunctella EST library using ortholog sequences of Bombyx mori. Both SOD and Tpx were expressed in larvae of P. interpunctella especially under oxidative stress induced by bacterial challenge. Exposure to ClO2 gas significantly induced the gene expression of both SOD and Tpx. RNA interference of SOD or Tpx using specific double stranded RNAs significantly enhanced the lethality of P. interpunctella to ClO2 gas treatment as well as to the bacterial challenge. These results suggest that ClO2 induces the production of insecticidal ROS, which results in a fatal oxidative stress in P. interpunctella.

  13. Oxidative stress induced by chlorine dioxide as an insecticidal factor to the Indian meal moth, Plodia interpunctella.

    Science.gov (United States)

    Kumar, Sunil; Park, Jiyeong; Kim, Eunseong; Na, Jahyun; Chun, Yong Shik; Kwon, Hyeok; Kim, Wook; Kim, Yonggyun

    2015-10-01

    A novel fumigant, chlorine dioxide (ClO2) is a commercial bleaching and disinfection agent. Recent study indicates its insecticidal activity. However, its mode of action to kill insects is yet to be understood. This study set up a hypothesis that an oxidative stress induced by ClO2 is a main factor to kill insects. The Indian meal moth, Plodia interpunctella, is a lepidopteran insect pest infesting various stored grains. Larvae of P. interpunctella were highly susceptible to ClO2 gas, which exhibited an acute toxicity. Physiological damages by ClO2 were observed in hemocytes. At high doses, the larvae of P. interpunctella suffered significant reduction of total hemocytes. At low doses, ClO2 impaired hemocyte behaviors. The cytotoxicity of ClO2 was further analyzed using two insect cell lines, where Sf9 cells were more susceptible to ClO2 than High Five cells. The cells treated with ClO2 produced reactive oxygen species (ROS). The produced ROS amounts increased with an increase of the treated ClO2 amount. However, the addition of an antioxidant, vitamin E, significantly attenuated the cytotoxicity of ClO2 in a dose-dependent manner. To support the oxidative stress induced by ClO2, two antioxidant genes (superoxide dismutase (SOD) and thioredoxin-peroxidase (Tpx)) were identified from P. interpunctella EST library using ortholog sequences of Bombyx mori. Both SOD and Tpx were expressed in larvae of P. interpunctella especially under oxidative stress induced by bacterial challenge. Exposure to ClO2 gas significantly induced the gene expression of both SOD and Tpx. RNA interference of SOD or Tpx using specific double stranded RNAs significantly enhanced the lethality of P. interpunctella to ClO2 gas treatment as well as to the bacterial challenge. These results suggest that ClO2 induces the production of insecticidal ROS, which results in a fatal oxidative stress in P. interpunctella. PMID:26453230

  14. Formation of iodinated disinfection by-products during oxidation of iodide-containing waters with chlorine dioxide.

    Science.gov (United States)

    Ye, Tao; Xu, Bin; Lin, Yi-Li; Hu, Chen-Yan; Lin, Lin; Zhang, Tian-Yang; Gao, Nai-Yun

    2013-06-01

    This study was to explore the formation of iodinated disinfection by-products (I-DBPs), including iodoform (CHI3), iodoacetic acid (IAA) and triiodoacetic acid (TIAA), when iodide-containing artificial synthesized waters and raw waters are in contact with chlorine dioxide (ClO2). Among the investigated I-DBPs, CHI3 was the major species during ClO2 oxidation in artificial synthesized waters. Impact factors were evaluated, including the concentrations of ClO2, iodide (I(-)), dissolved organic carbon (DOC) and pH. Formation of CHI3, IAA and TIAA followed an increasing and then decreasing pattern with increased ClO2 or DOC concentration. I-DBPs yield was significantly affected by solution pH. High concentrations of I-DBPs were generated under circumneutral conditions with the maximum formation at pH 8. The increase of I(-) concentration can increase I-DBPs yields, but the increment was suppressed when I(-) concentration was higher than 50 μM. When 100 μg/L I(-)and ClO2 (7.5-44.4 μM) were spiked to the raw water samples from Yangshupu and Minhang drinking water treatment plant, certain amounts of CHI3 and IAA were found under pH 7 and the concentrations were strongly correlated with ClO2 dosage and water qualities, however, no TIAA was detected. Finally, we investigated I-DBPs formation of 18 model compounds, including 4 carboxylic acids, 5 phenols and 8 amino acids, treating with ClO2 when I(-) was present. Results showed that most of these model compounds could form a considerable amount of I-DBPs, especially for propanoic acid, butanoic acid, resorcinol, hydroquinone, alanine, glutamic acid, phenylalanine and serine.

  15. Inactivation of Chironomid Larvae with Chlorine Dioxide and Chlorine

    Institute of Scientific and Technical Information of China (English)

    SUN Xin-bin; CUI Fu-yi

    2008-01-01

    Chironomid larvae propagate prolifically in eutrophic water body and they cannot be exterminated by conventional disinfection process.The inactivation effects of chlorine and chlorine dioxide on Chironomid larvae were investigated and some boundary values in practice were determined under conditions of various oxidant dosage,organic precursor concentration and pH value.In addition,removal effect of differmt pre-oxidation combined with coagulation process on Chironomid larvae in law water was evaluated.It was found that chlorine dioxide possessed better inactivation effect than chlorine.Complete inactivation of Chironomid larvae in raw water was resulted by 1.5mg/L of chlorine dioxide with 30min of contact time. Additionally,the ocgallic precursor concentration,pH value had little influence on the inactivation effect.The coagulation jar test showed that Chironomid larvae in the raw water could be completely ronxwed by chlorine dioxide pre-oxidation in combination with the omgulation process at chlorine dioxide dosage of 0.8 mg/L.

  16. Transformation of iopamidol during chlorination.

    Science.gov (United States)

    Wendel, Friedrich M; Lütke Eversloh, Christian; Machek, Edward J; Duirk, Stephen E; Plewa, Michael J; Richardson, Susan D; Ternes, Thomas A

    2014-11-01

    The transformation of the iodinated X-ray contrast media (ICM) iopamidol, iopromide, iohexol, iomeprol, and diatrizoate was examined in purified water over the pH range from 6.5 to 8.5 in the presence of sodium hypochlorite, monochloramine, and chlorine dioxide. In the presence of aqueous chlorine, only iopamidol was transformed. All other ICM did not show significant reactivity, regardless of the oxidant used. Chlorination of iopamidol followed a second order reaction, with an observed rate constant of up to 0.87 M(-1) s(-1) (±0.021 M(-1) s(-1)) at pH 8.5. The hypochlorite anion was identified to be the reactive chlorine species. Iodine was released during the transformation of iopamidol, and was mainly oxidized to iodate. Only a small percentage (less than 2% after 24 h) was transformed to known organic iodinated disinfection byproducts (DBPs) of low molecular weight. Some of the iodine was still present in high-molecular weight DBPs. The chemical structures of these DBPs were elucidated via MSn fragmentation and NMR. Side chain cleavage was observed as well as the exchange of iodine by chlorine. An overall transformation pathway was proposed for the degradation of iopamidol. CHO cell chronic cytotoxicity tests indicate that chlorination of iopamidol generates a toxic mixture of high molecular weight DBPs (LC50 332 ng/μL).

  17. Chlorinated indium tin oxide electrode by InCl3 aqueous solution for high-performance organic light-emitting diodes

    Science.gov (United States)

    Hu, Yun; Zhou, Dong-Ying; Wang, Bo; Wang, Zhao-Kui; Liao, Liang-Sheng

    2016-04-01

    The authors develop a facile and effective method to produce the chlorinated indium tin oxide (Cl-ITO) treated by InCl3 aqueous solution and UV/ozone. The work function of the Cl-ITO achieved by this treatment is as high as 5.69 eV, which is increased by 1.09 eV compared with that of the regular ITO without any treatment. Further investigation proved that the enhancement of the work function is attributed to the formation of In-Cl bonds on the Cl-ITO surface. Green phosphorescent organic light-emitting devices based on the Cl-ITO electrodes exhibit excellent electroluminescence performance, elongating lifetime due to the improvement in hole injection.

  18. Application of in situ chemical oxidation technique with potassium permanganate for the remediation of a shallow aquifer contaminated with chlorinated solvents

    Directory of Open Access Journals (Sweden)

    Alaine Santos da Cunha

    2012-12-01

    Full Text Available In situ chemical oxidation is a method that is frequently being used for the remediation of contaminated areas, since it presents an adequate efficiency in the reduction of the contaminant mass, particularly chlorinated ethenes, in a relatively short period of time. This manuscript presents the results of the application of this method, using the injection of potassium permanganate as the remediation agent, in an impacted area with chlorinated organic compounds, especially 1,1-dichloroethene. The effectiveness of this remediation method is related to the complexity of the conceptual model of the contaminated site and to the conduction of specific studies in laboratory and pilot tests in field scale, prior to the accomplishment of the full-scale remediation. Therefore, this work contributes presenting a description of the procedures that are commonly used for conducting this kind of studies. In the case under study, it was estimated that the mass of 1.1-dichloroethene (1.1-DCE was reduced from 15.53 to 1.81 kg in groundwater 22 months after the injection of potassium permanganate in the aquifer. The average concentrations of 1.1-DCE in groundwater decreased from 200 to 24 g/L, which value is lower than the environmental standard limit and also to the calculated target of remediation based on human-health risk assessment. Significant contamination rebounds were not identified in the aquifer after the injection of the chemical oxidant. The suitable results of the remediation in this case may be related to the relatively low aquifer heterogeneity and low original concentrations of the contaminant.

  19. Impact of UV/H2O2 pre-oxidation on the formation of haloacetamides and other nitrogenous disinfection byproducts during chlorination.

    Science.gov (United States)

    Chu, Wenhai; Gao, Naiyun; Yin, Daqiang; Krasner, Stuart W; Mitch, William A

    2014-10-21

    Haloacetamides (HAcAms), an emerging class of nitrogen-based disinfection byproducts (N-DBPs) of health concern in drinking water, have been found in drinking waters at μg/L levels. However, there is a limited understanding about the formation, speciation, and control of halogenated HAcAms. Higher ultraviolet (UV) doses and UV advanced oxidation (UV/H2O2) processes (AOPs) are under consideration for the treatment of trace organic pollutants. The objective of this study was to examine the potential of pretreatment with UV irradiation, H2O2 oxidation, and a UV/H2O2 AOP for minimizing the formation of HAcAms, as well as other emerging N-DBPs, during postchlorination. We investigated changes in HAcAm formation and speciation attributed to UV, H2O2 or UV/H2O2 followed by the application of free chlorine to quench any excess hydrogen peroxide and to provide residual disinfection. The results showed that low-pressure UV irradiation alone (19.5-585 mJ/cm(2)) and H2O2 preoxidation alone (2-20 mg/L) did not significantly change total HAcAm formation during subsequent chlorination. However, H2O2 preoxidation alone resulted in diiodoacetamide formation in two iodide-containing waters and increased bromine utilization. Alternatively, UV/H2O2 preoxidation using UV (585 mJ/cm(2)) and H2O2 (10 mg/L) doses typically employed for trace contaminant removal controlled the formation of HAcAms and several other N-DBPs in drinking water.

  20. Attacks of Asthma due to Chlorinized Water: Case Report

    OpenAIRE

    Murat Eyup Berdan; Ercan Gocgeldi; Sami Ozturk; Ali Kutlu

    2008-01-01

    The presence of a high prevalence of bronchial hyperresponsiveness and asthma-like symptoms in swimmers has been reported. But, attacks of asthma which is related to chlorinized water is rare. Chlorine, a strong oxidizing agent, is an important toxic gas that the swimmer can breath during swimming and a worker can exposed to chlorine while he or she was using water with chlorine at home. We describe a persistent increase in nonspecific bronchial hyperresponsiveness following chronic exposure ...

  1. Internal chlorination of Ni-Cr alloys

    Energy Technology Data Exchange (ETDEWEB)

    Berztiss, D.; Hennesen, K.; Grabke, H.J. [Max-Planck-Institut fuer Eisenforschung GmbH, Duesseldorf (Germany)

    1998-12-31

    In contrast to internal oxidation, sulfidation and carburization, very little information is available regarding internal chlorination, especially diffusion of chlorine in metallic alloys. This paper describes results of experiments on Ni-Cr alloys (<10 wt% Cr) exposed in an atmosphere containing radioactive HCl. The diffusion of chlorine in the alloy can be determined by measurement of residual {beta}-activity from the sample surface. Successively thin layers (0.5-10 {mu}m) of the alloy were removed by lapping and the surface activity was measured to obtain a depth profile. Both single and polycrystalline materials were tested. Through this work it should be determined if there is in fact solubility and diffusion of chlorine in Ni-based alloys as some authors have proposed or if the ingress of chlorine is mainly a grain boundary phenomenon. (orig.)

  2. Kinetic studies on dissolution of UO2 powders in acid solutions by using cerium (IV) or chlorine dioxide as oxidants

    International Nuclear Information System (INIS)

    The UO2 powders of 100-150, 150-212, 212-250, and 250-300 μm were dissolved in HNO3 or HCl solutions containing strong oxidants to examine their effect on the dissolution rates. Cerium(IV) species and ClO2 were used as oxidants in HNO3 and HCl solutions, respectively. The Ce(IV) species were prepared by bubbling O3 gas into HNO3 solutions containing Ce(NO3)3. All dissolution experiments were carried out under rapid stirring conditions which make it possible to neglect the diffusion effect. Dissolution reactions were analyzed on the assumptions that the UO2 powders are spherical particles and homogeneously dissolved from their external surface. Dissolution rate constants (Φ) in mol·cm-2·min-1 were measured at various concentrations of oxidants and temperatures. Furthermore, the effect of acid concentrations on the dissolution rate was also examined. As a result, the dissolution rate constants Φ were found to be expressed as Φ=kN[Ce(IV)][H+]0.6 for HNO3 solution([HNO3]=1-5M, Temp.≤30degC) and Φ=kH[ClO2][H+]-0.3 for HCl solution([HCl]=1-5M, Temp.≤30degC), respectively. Activation energies(kJ·mol-1) for the apparent dissolution rate constants are 44.1±1.9 for the HNO3 solution system and 33.5±2.8 for the HCl solution system, respectively. (author)

  3. Technology assessment: Chlorine chemistry

    International Nuclear Information System (INIS)

    Chlorine is not just one of many chemical feedstocks which is used in a few definitely harmful products like PVC or CFC but is irrelevant in all other respects. Just the opposite is true: There is hardly any product line of the chemical industry that can do without chlorine, from herbicides and pesticides to dyes, plastics, pharmaceuticals, photographic atricles, and cosmetics. Chlorine is not only a key element of chemical production but also an ubiquitous element of everyday life in civilisation. There are even many who would agree that the volume of chlorine production is an indicator of the competitive strength and national wealth of a modern society. By now, however, it has become evident that the unreflected use of chlorine is no longer ecologically acceptable. The consequences of a chlorine phase-out as compared to the continued chlorine production at the present level were investigated scientifically by a PROGNOS team. They are presented in this book. (orig.)

  4. Removal of iodide from water by chlorination and subsequent adsorption on powdered activated carbon

    OpenAIRE

    Ikari, Mariya; Matsui, Yoshihiko; Suzuki, Yuta; Matsushita, Taku; Shirasaki, Nobutaka

    2015-01-01

    Chlorine oxidation followed by treatment with activated carbon was studied as a possible method for removing radioactive iodine from water. Chlorination time, chlorine dose, the presence of natural organic matter (NOM), the presence of bromide ion (Br-), and carbon particle size strongly affected iodine removal. Treatment with superfine powdered activated carbon (SPAC) after 10-min oxidation with chlorine (1 mg-Cl-2/L) removed 90% of the iodine in NOM-containing water (dissolved organic carbo...

  5. Transformation of cefazolin during chlorination process: products, mechanism and genotoxicity assessment.

    Science.gov (United States)

    Li, Liping; Wei, Dongbin; Wei, Guohua; Du, Yuguo

    2013-11-15

    Large quantities of cephalosporins have entered into aquatic environment in recent years, posing potential adverse effect to human health and ecological safety. In this study, cefazolin, one of widely used cephalosporins, was targeted to explore its transformation behaviors in chlorination disinfection process. With the help of ultra high performance liquid chromatography and high resolution mass spectroscopy, one chlorinated product and four oxidation products were detected in cefazolin chlorination system. The corresponding transformation pathways of cefazolin were proposed. Two kinds of reactions occurred in chlorination system, one was oxidation of thioether-sulfur to sulfoxide and di-sulfoxide, and the other was base-catalyzed electrophilic substitution of alpha-H of amide by chlorine atom. The pH value determined the occurrence of reaction types, and increasing chlorine dose promoted transformation of cefazolin. More importantly, genotoxicity in SOS/umu assay had an elevation after chlorination, which might be attributed to the formation of chlorinated product and sulfoxide during chlorination process.

  6. Influencing factors and degradation products of antipyrine chlorination in water with free chlorine

    Institute of Scientific and Technical Information of China (English)

    Meiquan Cai; Liqiu Zhang; Fei Qi; Li Feng

    2013-01-01

    Owing to its low cost,free chlorine is one of the most common disinfectants for wastewater and drinking water treatment.However,the formation of disinfection byproducts has been found to occur after free chlorine disinfection in recent decades.Antipyrine (ANT),an anti-inflammatory analgesic,has been frequently detected in the aquatic environment.In this work.the removal efficiency of ANT by free chlorine oxidation in ultrapure water was investigated with batch experiments.The influencing factors on the removal of ANT were explored at initial concentrations of ANT from 0.04 to 0.64 mg/L,free chlorine dosage from 0.30 to 1.31 mg/L,and pH from 1.5 to 9.0.The main degradation products were identified by solid phase extraction-gas chromatography-mass spectrometry.The results showed that ANT reacted rapidly with free chlorine in ultrapure water systems and up to 90.6% removal efficiency of ANT was achieved after 25 sec (initial free chlorine 1 mg/L,ANT 0.5 mg/L,pH 7.0).Higher oxidant dosage,lower ANT initial concentration and low pH favor the ANT removal.The main degradation product in ANT chlorination was a monochlorine substitution product (4-chloro-l,2-dihydro1,5-dimethyl-2-phenyl-3H-pyrazol-3-one),which can be further chlorinated by free chlorine.In addition,the total organic carbon result indicated that ANT is difficult to be mineralized using chlorine.

  7. Influencing factors and degradation products of antipyrine chlorination in water with free chlorine.

    Science.gov (United States)

    Cai, Meiquan; Zhang, Liqiu; Qi, Fei; Feng, Li

    2013-01-01

    Owing to its low cost, free chlorine is one of the most common disinfectants for wastewater and drinking water treatment. However, the formation of disinfection byproducts has been found to occur after free chlorine disinfection in recent decades. Antipyrine (ANT), an anti-inflammatory analgesic, has been frequently detected in the aquatic environment. In this work, the removal efficiency of ANT by free chlorine oxidation in ultrapure water was investigated with batch experiments. The influencing factors on the removal of ANT were explored at initial concentrations of ANT from 0.04 to 0.64 mg/L, free chlorine dosage from 0.30 to 1.31 mg/L, and pH from 1.5 to 9.0. The main degradation products were identified by solid phase extraction-gas chromatography-mass spectrometry. The results showed that ANT reacted rapidly with free chlorine in ultrapure water systems and up to 90.6% removal efficiency of ANT was achieved after 25 sec (initial free chlorine 1 mg/L, ANT 0.5 mg/L, pH 7.0). Higher oxidant dosage, lower ANT initial concentration and low pH favor the ANT removal. The main degradation product in ANT chlorination was a monochlorine substitution product (4-chloro-1,2-dihydro-1,5-dimethyl-2-phenyl-3H-pyrazol-3-one), which can be further chlorinated by free chlorine. In addition, the total organic carbon result indicated that ANT is difficult to be mineralized using chlorine.

  8. 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.

  9. Chlorinated and nitrogenous disinfection by-product formation from ozonation and post-chlorination of natural organic matter surrogates.

    Science.gov (United States)

    Bond, Tom; Templeton, Michael R; Rifai, Omar; Ali, Hussain; Graham, Nigel J D

    2014-09-01

    Ozonation before chlorination is associated with enhanced formation of chloropicrin, a halonitromethane disinfection by-product (DBP), during drinking water treatment. In order to elucidate reasons for this, five natural organic matter (NOM) surrogates were treated using both chlorination and ozonation-chlorination under controlled laboratory conditions. Selected surrogates comprised two phenolic compounds, two free amino acids and one dipeptide; these were resorcinol, 3-aminophenol, L-aspartic acid, β-alanine and ala-ala, respectively. Quantified DBPs included chloropicrin, chloroform, dichloroacetonitrile and trichloroacetonitrile. Relative to chlorination alone, increases in the formation of chloropicrin from ozonation-chlorination varied from 138% for 3-aminophenol to 3740% for ala-ala for the four amine surrogates. This indicates that ozone is more effective than chlorine in mediating a rate-limiting oxidation step in chloropicrin formation, most plausibly involving conversion of an amine group to a nitro group. While both hydrophilic and hydrophobic surrogates acted as chloropicrin precursors, ala-ala was the most reactive precursor following ozonation-chlorination. Since peptides are far commoner in drinking water sources than free amino acids, further research into chemical oxidation of these species by ozone and chlorine is recommended. In contrast, oxidation with ozone prior to chlorination reduced chloroform formation moderately for the two phenolic compounds.

  10. Transformation of cefazolin during chlorination process: Products, mechanism and genotoxicity assessment

    Energy Technology Data Exchange (ETDEWEB)

    Li, Liping, E-mail: lisaleercees807@yahoo.cn; Wei, Dongbin, E-mail: weidb@rcees.ac.cn; Wei, Guohua, E-mail: wgh@rcees.ac.cn; Du, Yuguo, E-mail: duyuguo@rcees.ac.cn

    2013-11-15

    Highlights: • Base-catalyzed electrophilic substitution occurred in cefazolin chlorination. • Oxidation of thioether in cefazolin was found in chlorination process. • The pH conditions impacted on the occurrence of reaction types. • Genotoxicity had an elevation after chlorination of cefazolin. • Reaction pathways of cefazolin chlorination were replayed in surface water matrix. -- Abstract: Large quantities of cephalosporins have entered into aquatic environment in recent years, posing potential adverse effect to human health and ecological safety. In this study, cefazolin, one of widely used cephalosporins, was targeted to explore its transformation behaviors in chlorination disinfection process. With the help of ultra high performance liquid chromatography and high resolution mass spectroscopy, one chlorinated product and four oxidation products were detected in cefazolin chlorination system. The corresponding transformation pathways of cefazolin were proposed. Two kinds of reactions occurred in chlorination system, one was oxidation of thioether-sulfur to sulfoxide and di-sulfoxide, and the other was base-catalyzed electrophilic substitution of alpha-H of amide by chlorine atom. The pH value determined the occurrence of reaction types, and increasing chlorine dose promoted transformation of cefazolin. More importantly, genotoxicity in SOS/umu assay had an elevation after chlorination, which might be attributed to the formation of chlorinated product and sulfoxide during chlorination process.

  11. Fate of free chlorine in drinking water during distribution in premise plumbing.

    Science.gov (United States)

    Zheng, Muzi; He, Chunguang; He, Qiang

    2015-12-01

    Free chlorine is a potent oxidizing agent and has been used extensively as a disinfectant in processes including water treatment. The presence of free chlorine residual is essential for the prevention of microbial regrowth in water distribution systems. However, excessive levels of free chlorine can cause adverse health effects. It is a major challenge to maintain appropriate levels of free chlorine residual in premise plumbing. As the first effort to assessing the fate of chlorine in premise plumbing using actual premise plumbing pipe sections, three piping materials frequently used in premise plumbing, i.e. copper, galvanized iron, and polyvinyl chloride (PVC), were investigated for their performance in maintaining free chlorine residual. Free chlorine decay was shown to follow first-order kinetics for all three pipe materials tested. The most rapid chlorine decay was observed in copper pipes, suggesting the need for higher chlorine dosage to maintain appropriate levels of free chlorine residual if copper piping is used. PVC pipes exhibited the least reactivity with free chlorine, indicative of the advantage of PVC as a premise plumbing material for maintaining free chlorine residual. The reactivity of copper piping with free chlorine was significantly hindered by the accumulation of pipe deposits. In contrast, the impact on chlorine decay by pipe deposits was not significant in galvanized iron and PVC pipes. Findings in this study are of great importance for the development of effective strategies for the control of free chlorine residual and prevention of microbiological contamination in premise plumbing.

  12. Fate of free chlorine in drinking water during distribution in premise plumbing.

    Science.gov (United States)

    Zheng, Muzi; He, Chunguang; He, Qiang

    2015-12-01

    Free chlorine is a potent oxidizing agent and has been used extensively as a disinfectant in processes including water treatment. The presence of free chlorine residual is essential for the prevention of microbial regrowth in water distribution systems. However, excessive levels of free chlorine can cause adverse health effects. It is a major challenge to maintain appropriate levels of free chlorine residual in premise plumbing. As the first effort to assessing the fate of chlorine in premise plumbing using actual premise plumbing pipe sections, three piping materials frequently used in premise plumbing, i.e. copper, galvanized iron, and polyvinyl chloride (PVC), were investigated for their performance in maintaining free chlorine residual. Free chlorine decay was shown to follow first-order kinetics for all three pipe materials tested. The most rapid chlorine decay was observed in copper pipes, suggesting the need for higher chlorine dosage to maintain appropriate levels of free chlorine residual if copper piping is used. PVC pipes exhibited the least reactivity with free chlorine, indicative of the advantage of PVC as a premise plumbing material for maintaining free chlorine residual. The reactivity of copper piping with free chlorine was significantly hindered by the accumulation of pipe deposits. In contrast, the impact on chlorine decay by pipe deposits was not significant in galvanized iron and PVC pipes. Findings in this study are of great importance for the development of effective strategies for the control of free chlorine residual and prevention of microbiological contamination in premise plumbing. PMID:26407709

  13. Attacks of Asthma due to Chlorinized Water: Case Report

    Directory of Open Access Journals (Sweden)

    Murat Eyup Berdan

    2008-02-01

    Full Text Available The presence of a high prevalence of bronchial hyperresponsiveness and asthma-like symptoms in swimmers has been reported. But, attacks of asthma which is related to chlorinized water is rare. Chlorine, a strong oxidizing agent, is an important toxic gas that the swimmer can breath during swimming and a worker can exposed to chlorine while he or she was using water with chlorine at home. We describe a persistent increase in nonspecific bronchial hyperresponsiveness following chronic exposure to strong respiratory irritant with chlorinized water in two subjects with no past history of asthma or atopy. We conclude that airway hyperresponsiveness can develop or increase after chronic inhalation of high concentrations of irritants such as chlorinized water an indoor irritant factor and that these changes may be prolonged. [TAF Prev Med Bull. 2008; 7(1: 87-90

  14. Attacks of Asthma due to Chlorinized Water: Case Report

    Directory of Open Access Journals (Sweden)

    Murat Eyup Berdan

    2008-02-01

    Full Text Available The presence of a high prevalence of bronchial hyperresponsiveness and asthma-like symptoms in swimmers has been reported. But, attacks of asthma which is related to chlorinized water is rare. Chlorine, a strong oxidizing agent, is an important toxic gas that the swimmer can breath during swimming and a worker can exposed to chlorine while he or she was using water with chlorine at home. We describe a persistent increase in nonspecific bronchial hyperresponsiveness following chronic exposure to strong respiratory irritant with chlorinized water in two subjects with no past history of asthma or atopy. We conclude that airway hyperresponsiveness can develop or increase after chronic inhalation of high concentrations of irritants such as chlorinized water an indoor irritant factor and that these changes may be prolonged. [TAF Prev Med Bull 2008; 7(1.000: 87-90

  15. An Experimental Study of Removing Sulfur Dioxide and Nitrogen Oxides by Stabilized Chlorine Dioxide%稳定性二氧化氯脱氮除硫实验研究

    Institute of Scientific and Technical Information of China (English)

    王春慧; 晋日亚; 池致超; 宋相丹

    2011-01-01

    实验以稳定性二氧化氯溶液作为吸收液,采用气液逆流操作,研究了填料高度、二氧化氟溶液的质量浓度及溶液的pH值等因素对稳定性二氧化氯脱氮除硫效果的影响.实验结果表明:二氧化氯的质量浓度对去除率的影响最大,溶液的pH值对去除率的影响较小,不论在酸性或碱性的条件下都能达到较高的去除率.当填料高度大于20 cm,二氧化氯的质量浓度为0.6 g/L,溶液的pH值为3.47时,NOx和SO2的去除率分别达到90%和99.95%以上.%In the experiment, stabilized chlorine dioxide solution was used as absorbent and gas-liquid countercurrent was adopted in operation. The effects of packing height, mass concentration of chlorine dioxide solution and solution pH value, etc.on the efficiency of removal rate of sulfur dioxide and nitrogen oxides by stabilized chlorine dioxide were investigated. The results show that the mass concentration of chlorine dioxide has the greatest impact on the removal rate and the pH value is of less influence on the removal rate. The removal rate can reach a higher level under both acidic and alkaline conditions. When the packing height is greater than 20 cm, chlorine dioxide concentration is 0.6 g/L, pH is 3.47, the removal rates of NOx and SO2 can reach 90 % and 99.95 % respectively.

  16. Water Treatment Technology - Chlorination.

    Science.gov (United States)

    Ross-Harrington, Melinda; Kincaid, G. David

    One of twelve water treatment technology units, this student manual on chlorination provides instructional materials for nine competencies. (The twelve units are designed for a continuing education training course for public water supply operators.) The competencies focus on the following areas: purpose and process of chlorination, chlorine…

  17. Chlorination of organophosphorus pesticides in natural waters.

    Science.gov (United States)

    Acero, Juan L; Benítez, F Javier; Real, Francisco J; González, Manuel

    2008-05-01

    Unknown second-order rate constants for the reactions of three organophosphorus pesticides (chlorpyrifos, chlorfenvinfos and diazinon) with chlorine were determined in the present study, and the influence of pH and temperature was established. It was found that an increase in the pH provides a negative effect on the pesticides degradation rates. Apparent second-order rate constants at 20 degrees C and pH 7 were determined to be 110.9, 0.004 and 191.6 M(-1) s(-1) for chlorpyrifos, chlorfenvinfos and diazinon, respectively. A higher reactivity of chlorine with the phosphorothioate group (chlorpyrifos and diazinon) than with the phosphate moiety (chlorfenvinfos) could explain these results. Intrinsic rate constant for the elementary reactions of chlorine species with chlorpyrifos and diazinon were also calculated, leading to the conclusion that the reaction between hypochlorous acid and the pesticide is predominant at neutral pH. The elimination of these pesticides in surface waters was also investigated. A chlorine dose of 2.5 mg L(-1) was enough to oxidize chlorpyrifos and diazinon almost completely, with a formation of trihalomethanes below the EU standard for drinking water. However, the removal of chlorfenvinfos was not appreciable. Therefore, chlorination is a feasible option for the removal of organophosphorus pesticides with phosphorothioate group during oxidation and disinfection processes, but not for the elimination of pesticides with phosphate moiety.

  18. 46 CFR 151.50-31 - Chlorine.

    Science.gov (United States)

    2010-10-01

    ... desired rate of discharge, provided the air or gas is oil-free and thoroughly dried by passing it over activated aluminum oxide, silica gel, or other acceptable drying agent, and provided the supply pressure is...-resistant to chlorine in either the gas or liquid phase. Cast or malleable iron shall not be used....

  19. 钌镧氧化物涂层析氯反应动力学比较研究%Comparative Study on Kinetics of Chlorine Evolution Reaction for Ru-La-O Oxide Coatings

    Institute of Scientific and Technical Information of China (English)

    龙萍; 许立坤; 崔秀芳; 金国

    2015-01-01

    通过热分解法制备了Ti/RuO2和Ti/Ru-La-O氧化物涂层,利用微分电容和极化曲线等实验方法对涂层Clˉ特性吸附、La对RuO2涂层析氯反应过程的影响及反应机理进行了研究.结果表明,在NaCl溶液中,涂层表面存在Clˉ的特性吸附,这种特性吸附对析氯反应的动力学产生了影响,导致Tafel斜率上升,反应级数下降,加入La使氧化钌涂层的过电位下降,交换电流密度增大,有利于析氯反应的进行.本文对涂层存在的两种可能反应机理进行了比较分析,认为在中性NaCl溶液中析氯反应是由2≡S·OCl*(rds→)≡S·O +Cl2过程控制的.%The Ti/RuO2 and Ti/Ru-La-O oxide coatings were prepared by thermal decomposition of the metal chlorides in the precursor solution. The specific adsorption of Clˉ on coatings, the effect of La on the chlorine evo-lution reactions (ClER) and the kinetic mechanism were investigated by using differential capacity (DC) and po-larization curves (PC). Results show that the coating surface exhibits significantly specific adsorption of Clˉ in NaCl neutral solution, which has an influence on the kinetics of the chlorine evolution process, resulting in an in-crease of the Tafel slope and a decrease of the reaction order. The addition of lanthanum reduces the overpotential of Ti/RuO2 coating and enhances the exchange current density, which improves the chlorine evolution reaction of the coatings. Both kinetic mechanisms of recombination and electrochemical desorption of adsorbed intermediate species for the coatings are comparatively studied. It is confirmed that the Chlorine evolution reaction on Ru-La-O oxide coatings in NaCl neutral solution is controlled by the process of 2≡ S· OCl* (rds→)≡ S·O +Cl2.

  20. Metals releases and disinfection byproduct formation in domestic wells following shock chlorination

    OpenAIRE

    Walker, M.; Newman, J.

    2010-01-01

    Shock chlorination is used for rapid disinfection to control pathogens and nuisance bacteria in domestic wells. A typical shock chlorination procedure involves adding sodium hypochlorite in liquid bleach solutions to achieve concentrations of free chlorine of up to 200 ppm in the standing water of a well. The change in pH and oxidation potential may bring trace metals from aquifer materials into solution and chlorine may react with dissolved organic carbon to form disinfection byproducts. We ...

  1. Study on encapsulation of chlorine dioxide in gelatin microsphere for reducing release rate

    OpenAIRE

    Ci, Ying; Wang, Lin; Guo, YanChuan; Sun, Ruixue; Wang, Xijie; Li, Jinyou

    2015-01-01

    Objective: This study aims to explore the effects of encapsulation of chlorine dioxide in a hydrophilic biodegradable polymer gelatin to reduce its release rate. Methods: An emulsification-coacervation method was adopted. The characterizations of chlorine dioxide-gelatin microspheres were described. Using UV-vis spectrophotometer the λmax of chlorine dioxide was observed at 358 nm. The particle size and distribution of chlorine oxide-gelatin microspheres was measured by a dynamic light scatte...

  2. Chlorination of nickel ore by gaseous chlorine in the presence of active additives

    Directory of Open Access Journals (Sweden)

    Ilić Ilija B.

    2003-01-01

    Full Text Available Paper presents a thermodynamic analysis of chemical reactions occurring during chlorination with and without additives for both nickel oxides and nickel ferrites, which are component parts of nickel ore. The experimental research investigated the influence of temperature in the range from 600 up to 1000 °C and time (up to 3 h on the chlorination degree of nickel ores with and without additives. It was found that the introduction of additives such as C, S, BaS and NaCl intensified the chlorination of nickel ore. The results can be applied and may help determine the optimal conditions for the chlorination of low-grade ferrous nickel ores.

  3. Chapter 3. Chloric decomposition of aluminosilicate ores. 3.1. Features of chlorination of aluminium containing ores

    International Nuclear Information System (INIS)

    The features of chlorination of aluminium containing ores are considered in this article. Theoretical aspects of metals, oxides and natural compounds chlorination, specific features of synthesis of various chlorides are considered as well.

  4. Determination of chlorine in silicate rocks

    Science.gov (United States)

    Peck, L.C.

    1959-01-01

    In a rapid accurate method for the determination of chlorine in silicate rocks, the rock powder is sintered with a sodium carbonate flux containing zinc oxide and magnesium carbonate. The sinter cake is leached with water, the resulting solution is filtered, and the filtrate is acidified with nitric acid. Chlorine is determined by titrating this solution with mercuric nitrate solution using sodium nitroprusside as the indicator. The titration is made in the dark with a beam of light shining through the solution. The end point of the titration is found by visually comparing the intensity of this beam of light with that of a similar beam of light in a reference solution.

  5. Treatment of algae-induced tastes and odors by chlorine, chlorine dioxide and permanganate

    OpenAIRE

    Buffin, Lisa Webster

    1992-01-01

    Chlorine (C12(sq»' chlorine dioxide (Cl02 ) and potassium permanganate (KMn04) were evaluated as oxidants for the removal of grassy and cucumber odors associated with the pure compounds, cis-3-hexenol and trans-2, cis-6-nonadienal, respectively, and for the removal of fishy odors associated with a culture of an alga, Synura petersenii. The effects of the oxidants on the pure compounds were assessed both by Flavor Profile Analysis (FPA) and gas chromatography/mass spectrometry (GC/MS). The ef...

  6. Chlorination of pyrene in soil components with sodium chloride under xenon irradiation

    International Nuclear Information System (INIS)

    It was previously reported that chlorinated pyrenes (1-chloropyrene and dichloropyrene) were produced from pyrene in soil under sunlight irradiation. It was suggested that pyrene reacted with chlorine ion under sunlight. In this work, the formation of chlorinated pyrenes is investigated on 9 metallic oxides as soil components with pyrene and sodium chloride under xenon lamp irradiation. The chlorinated pyrenes as the reaction products were extracted with benzene:ethanol (4:1), and analyzed by GC/MS (SIM). The chlorinated pyrenes were produced in high amounts on 5 metallic oxides [silicon dioxides (quartz, silicic anhydride and silica gel forms) and titanium dioxides (rutile and anatase forms)] and in small amounts in 3 sorts of metallic oxides (aluminium oxide, magnesium oxide and ferric oxide), whereas they were not produced on calcium oxide. It was found that the yields of chlorinated pyrenes depended on the amounts of pyrene and chlorine ions in metallic oxides. In silicon dioxides, the yields of chlorinated pyrenes increased as the irradiation time was extended. In the titanium dioxides, the yields of chlorinated pyrenes had a peak at 0.5 – 1 hours irradiation of xenon lamp, and decreased as the irradiation time elapsed. (author)

  7. Mutual separation characteristics for binary oxides Y2O3-Ln2O3(Ln = Sc,La,Nd,Sm) using stepwise selective chlorination-chemical vapor transport reaction mediated by vapor complexes KLnCl4

    Institute of Scientific and Technical Information of China (English)

    孙艳辉; 陈振飞; 王之昌

    2004-01-01

    Mutual separation characteristics for binary oxide mixtures Y2 O3-Sc2 O3, Y2 O3-La2 O3, Y2 O3-Nd2 O3and Y2 O3-Sm2 O3 using a stepwise selective chlorination-chemical vapor transport(SC-CVT) reaction mediated by vapor complexes KLnCl4 were investigated. The total transported yields of the chlorides produced from the oxide mixtures are in the order of NdCl3 >SmCl3 >LaCl3 >YCl3 >ScCl3 , the main deposition temperature of the chlorides is in the order of ScCl3 <YCl3 <SmCl3 <NdCl3 <LaCl3, and the largest separation factor values are 1 100 for Y . Sc,14.88 for Y : La, 9.86 for Y . Nd and 16.45 for Y . Sm in the temperature range from 1 000 K to 1 120 K, while 157.7 for La : Y, 51.6 for Nd : Y and 12.4 for Sm : Y in the temperature range from 1 200 K to 1 300 K, respectively. The results were discussed on the difference of KScCl4, KYCl4 and KLnCl4 and the selective chlorination of binary oxides at 800 K. Furthermore, the separation characteristics of vapor rare earth complex KLnCl4 were studied compared with those of LnAlnCl3n+3.

  8. Reaction products of chlorine dioxide.

    OpenAIRE

    Stevens, A A

    1982-01-01

    Inspection of the available literature reveals that a detailed investigation of the aqueous organic chemistry of chlorine dioxide and systematic identification of products formed during water disinfection has not been considered. This must be done before an informed assessment can be made of the relative safety of using chlorine dioxide as a disinfectant alternative to chlorine. Although trihalomethanes are generally not formed by the action of chlorine dioxide, the products of chlorine dioxi...

  9. Breakpoint chlorination curves of greywater.

    Science.gov (United States)

    March, J G; Gual, M

    2007-08-01

    A study on chlorination of raw greywater with hypochlorite is reported in this paper. Samples were chlorinated in a variety of conditions, and residual chlorine (Cl2) was measured spectrophotometrically. For each sample, the chlorination curve (chlorine residuals versus chlorine dose) was obtained. Curves showed the typical hump-and-dip profile attributable to the formation and destruction of chloramines. It was observed that, after reactions with strong reductants and chloramines-forming compounds, the remaining organic matter exerted a certain demand of chlorine. The evolution of chlorination curves with addition of ammonia and dodecylbencene sulfonate sodium salt and with dilution of the greywater sample were studied. In addition, chlorination curves at several contact times have been obtained, resulting in slower chlorine decay in the hump zone than in the dip zone. In addition, the decay of coliforms in chlorinated samples was also investigated. It was found that, for a chlorination dosage corresponding to the maximum of the hump zone (average 8.9 mg Cl2/ L), samples were negative in coliforms after 10 to 30 minutes of contact time. After-growth was not observed within 3 days after chlorination. Implications in chlorination treatments of raw greywater can be derived from these results. PMID:17824528

  10. Formation of chlorinated lipids post-chlorine gas exposure.

    Science.gov (United States)

    Ford, David A; Honavar, Jaideep; Albert, Carolyn J; Duerr, Mark A; Oh, Joo Yeun; Doran, Stephen; Matalon, Sadis; Patel, Rakesh P

    2016-08-01

    Exposure to chlorine (Cl2) gas can occur during accidents and intentional release scenarios. However, biomarkers that specifically indicate Cl2 exposure and Cl2-derived products that mediate postexposure toxicity remain unclear. We hypothesized that chlorinated lipids (Cl-lipids) formed by direct reactions between Cl2 gas and plasmalogens serve as both biomarkers and mediators of post-Cl2 gas exposure toxicities. The 2-chloropalmitaldehyde (2-Cl-Pald), 2-chlorostearaldehyde (2-Cl-Sald), and their oxidized products, free- and esterified 2-chloropalmitic acid (2-Cl-PA) and 2-chlorostearic acid were detected in the lungs and plasma of mouse and rat models of Cl2 gas exposure. Levels of Cl-lipids were highest immediately post-Cl2 gas exposure, and then declined over 72 h with levels remaining 20- to 30-fold higher at 24 h compared with baseline. Glutathione adducts of 2-Cl-Pald and 2-Cl-Sald also increased with levels peaking at 4 h in plasma. Notably, 3-chlorotyrosine also increased after Cl2 gas exposure, but returned to baseline within 24 h. Intranasal administration of 2-Cl-PA or 2-Cl-Pald at doses similar to those formed in the lung after Cl2 gas exposure led to increased distal lung permeability and inflammation and systemic endothelial dysfunction characterized by loss of eNOS-dependent vasodilation. These data suggest that Cl-lipids could serve as biomarkers and mediators for Cl2 gas exposure and toxicity. PMID:27324796

  11. New ORP/pH based control strategy for chlorination and dechlorination of wastewater: pilot scale application.

    Science.gov (United States)

    Kim, H; Kwon, S; Han, S; Yu, M; Kim, J; Gong, S; Colosimo, M F

    2006-01-01

    Due to its efficiency and low capital demands, chlorination has been widely used for disinfection in many wastewater treatment plants. Since the oxidation power of free chlorine is bigger than combined chlorines which are formed from the reaction between chlorine and reducing agents in water (especially, NH4+ and organic nitrogen), for effective disinfection, excess amount of chlorine is added until all the reducing agents are oxidized and free chlorine is available. After chlorination, chlorine residues in wastewater are usually reduced with SO2 or sulfites before the treated wastewater is discharged, since they are toxic to aquatic life. Addition of excess amount of SO2 or sulfite should be avoided. Otherwise, they consume dissolved oxygen in a river or stream and may have adverse impact on the aquatic life. Determination of wastewater chlorine demand and of sulfite dosages for dechlorination has been a challenge to WWTP operators, due to the dynamic characteristics of wastewater. Recently, a new ORP/pH based approach to determine chlorine demand and sulfite dosage was proposed. The method utilizes significant points occurring on the pH and ORP profiles during chlorination and dechlorination titrations. In this study, the proposed automatic titration system has been implemented into a control system to optimize chlorine and sulfite doses for a pilot scale chlorination/dechlorination system. In short, the disinfection system with the pH/ORP based controller showed very successful results; complete inactivation of total coliforms, and almost zero residual chlorines and high DO in its effluent. PMID:16749451

  12. Chlorine, Chloramine, Chlorine Dioxide, and Ozone Susceptibility of Mycobacterium avium

    OpenAIRE

    Taylor, Robert H.; Joseph O. Falkinham; Norton, Cheryl D.; LeChevallier, Mark W.

    2000-01-01

    Environmental and patient isolates of Mycobacterium avium were resistant to chlorine, monochloramine, chlorine dioxide, and ozone. For chlorine, the product of the disinfectant concentration (in parts per million) and the time (in minutes) to 99.9% inactivation for five M. avium strains ranged from 51 to 204. Chlorine susceptibility of cells was the same in washed cultures containing aggregates and in reduced aggregate fractions lacking aggregates. Cells of the more slowly growing strains wer...

  13. Chlorine Dioxide Gas Treatment of Cantaloupe and Residue Analysis

    OpenAIRE

    Kaur, Simran

    2013-01-01

    Chlorine dioxide is a selective oxidant and powerful antimicrobial agent. Previous work has shown that treatment of cantaloupe with chlorine dioxide gas at 5 mg/L for 10 minutes results in a 4.6 and 4.3 log reduction of E. coli O157:H7 and L. monocytogenes respectively. A significant reduction (p Current analytical methods for chlorine dioxide and chloroxyanions are only applicable to aqueous samples. Some of these methods have been used to determine surface residues in treated products by...

  14. 氯气氧化分解草酸钴沉淀母液中的草酸%Oxidation of oxalic acid by chlorine in mother-liquor originated from precipitation of cobalt oxalate

    Institute of Scientific and Technical Information of China (English)

    田庆华; 易宇; 郭学益

    2011-01-01

    为有效去除草酸沉钴母液中残留的大量草酸,采用氯气作为氧化剂探索氧化分解母液中草酸的可行性.考察反应温度、反应时间、氯气用量、搅拌速度和钴离子浓度等因素对氧化效果的影响.确定了优化工艺条件:反应温度50℃,搅拌速度700 r/min,次氯酸钙150 g,6 mol/L盐酸550 mL,反应时间3h.在此条件下,草酸的氧化率可达97.9%,母液中残留的草酸质量浓度仅为0.42 g/L,处理后的母液可直接返回含钴物料的浸出,实现了工艺流程的闭路循环.%In order to remove the oxalic acid left in the mother-liquor originated from the precipitation of cobalt by oxalic acid, a novel method of using chlorine as the oxidant to decompose the oxalic acid was proposed. The main factors affecting the oxidation rate such as the solution temperature, reaction time, quantity of chlorine, stirring speed and Co2* concentration were investigated. The optimal conditions are as follows: 700 r/min of stirring speed, 150 g calcium hypochlorite, 550 mL of hydrochloric acid with concentration of 6 mol/L and 5 h of reaction time at 70 °C. Under these conditions, the oxidation rate of oxalic acid is 97.9% and the concentration of residual oxalic acid in mother liquor is only 0.42 g/L. The treated mother liquor can be returned directly for leaching cobalt. There is a closed circulation in the whole process.

  15. Synergistic effect between UV and chlorine (UV/chlorine) on the degradation of carbamazepine: Influence factors and radical species.

    Science.gov (United States)

    Wang, Wen-Long; Wu, Qian-Yuan; Huang, Nan; Wang, Ting; Hu, Hong-Ying

    2016-07-01

    For successful wastewater reclamation, advanced oxidation processes have attracted attention for elimination of emerging contaminants. In this study, the synergistic treatment with UV irradiation and chlorine (UV/chlorine) was used to degrade carbamazepine (CBZ). Neither UV irradiation alone nor chlorination alone could efficiently degraded CBZ. UV/chlorine oxidation showed a significant synergistic effect on CBZ degradation through generation of radical species (OH and Cl), and this process could be well depicted by pseudo first order kinetic. The degradation rate constants (kobs,CBZ) of CBZ increased linearly with increasing UV irradiance and chlorine dosage. The degradation of CBZ by UV/chlorine in acidic solutions was more efficient than that in basic solutions mainly due to the effect of pH on the dissociation of HOCl and OCl(-) and then on the quantum yields and radical species quenching of UV/chlorine. When pH was increased from 5.5 to 9.5, the rate constants of degradation of CBZ by OH decreased from 0.65 to 0.14 min(-1) and that by Cl decreased from 0.40 to 0.11 min(-1). The rate constant for the reaction between Cl and CBZ was 5.6 ± 1.6 × 10(10) M(-1) s(-1). Anions of HCO3(-) (1-50 mM) showed moderate inhibition of CBZ degradation by UV/chlorine, while Cl(-) did not. UV/chlorine could efficiently degrade CBZ in wastewater treatment plant effluent, although the degradation was inhibited by about 30% compared with that in ultrapure water with chlorine dosage of 0.14-0.56 mM. Nine main oxidation products of the CBZ degradation by UV/chlorine were identified using the HPLC-QToF MS/MS. Initial oxidation products arose from hydroxylation, carboxylation and hydrogen atom abstraction of CBZ by OH and Cl, and were then further oxidized to generate acylamino cleavage and decarboxylation products of acridine and acridione. PMID:27105033

  16. Total catalytic wet oxidation of phenol and its chlorinated derivates with MnO{sub 2}/CeO{sub 2} catalyst in a slurry

    Energy Technology Data Exchange (ETDEWEB)

    Luna, A.J. [Instituto Nacional de Propriedade Industrial (INPI), Rio de Janeiro, RJ (Brazil)], e-mail: airtonj@inpi.gov.br; Rojas, L.O.A.; Sousa, J.F. de [Universidade Federal do Rio Grande do Norte (UFRN), Natal, RN (Brazil). Dept. of Chemical Engineering; Melo, D.M.A. [Universidade Federal do Rio Grande do Norte (UFRN), Natal, RN (Brazil). Dept. of Chemistry; Benachour, M. [Universidade Federal de Pernambuco (UFPE)Recife, PE (Brazil). Dept. of Chemical Engineering

    2009-07-15

    In the present work, a synthetic effluent of phenol was treated by means of a total oxidation process - Catalyzed Wet Oxidation (CWO). A mixed oxide of Mn-Ce (7:3), the catalyst, was synthesized by co-precipitation from an aqueous solution of MnCl{sub 2} and CeCl{sub 3} in a basic medium. The mixed oxide, MnO{sub 2}/CeO{sub 2}, was characterized and used in the oxidation of phenol in a slurry reactor in the temperature range of 80-130 deg C and pressure of 2.04-4.76 MPa. A phenol solution containing 2.4-dichlorophenol and 2.4- dichlorophenoxyacetic acid was also degraded with good results. A lumped kinetic model, with two parallel reaction steps, fits precisely with the integrated equation and the experimental data. The kinetic parameters obtained are in agreement with the Arrhenius equation. The activation energies were determined to be 38.4 for the total oxidation and 53.4 kJ/mol for the organic acids formed. (author)

  17. Total catalytic wet oxidation of phenol and its chlorinated derivates with MnO2/CeO2 catalyst in a slurry

    Directory of Open Access Journals (Sweden)

    A. J. Luna

    2009-09-01

    Full Text Available In the present work, a synthetic effluent of phenol was treated by means of a total oxidation process-Catalyzed Wet Oxidation (CWO. A mixed oxide of Mn-Ce (7:3, the catalyst, was synthesized by co-precipitation from an aqueous solution of MnCl2 and CeCl3 in a basic medium. The mixed oxide, MnO2/CeO2, was characterized and used in the oxidation of phenol in a slurry reactor in the temperature range of 80-130ºC and pressure of 2.04-4.76 MPa. A phenol solution containing 2.4-dichlorophenol and 2.4-dichlorophenoxyacetic acid was also degraded with good results. A lumped kinetic model, with two parallel reaction steps, fits precisely with the integrated equation and the experimental data. The kinetic parameters obtained are in agreement with the Arrhenius equation. The activation energies were determined to be 38.4 for the total oxidation and 53.4 kJ/mol for the organic acids formed.

  18. Removal effect on Mesocyclops leukarti and mutagenicity with chlorine dioxide

    Institute of Scientific and Technical Information of China (English)

    ZUO Jin-long; CUI Fu-yi; QU Bo; ZHU Gui-bing

    2006-01-01

    Mesocyclops leukarti of zooplankton propagates excessively in eutrophic water body and it cannot be effectively inactivated by the conventional drinking water treatment process. In order to tackle this problem, a study of removal effect on Mesocyclops leukarti with chlorine dioxide in a waterworks was performed. The results showed that Mesocyclops leukarti could be effectively removed from water by 1.0 mg/L chlorine dioxide preoxidation combined with the conventional drinking water treatment process.Higher oxidizability and molecular state of chlorine dioxide in water is the key to the inactivation of Mesocyclops leukarti. The chlorite, disinfection by-products (DBPs) of chlorine dioxide, was stable at 0.45 mg/L, which is lower than that critical value of the USEPA. GC-MS examination showed that the quantity of organic substance in the water treated by chlorine dioxide obviously decreased. Ames test further revealed that the mutagenicity was reduced by chlorine dioxide with respect to prechlorine. The propagation ofMesocyclops leukarti can be inactivated effectively and safely by chlorine dioxide pre-oxidation.

  19. Investigation of chlorination of zirconium and hafnium and their compounds in discharge from hollow cathode

    International Nuclear Information System (INIS)

    The possibility is investigated of chlorinating various zirconium and hafnium compounds (metal, oxide, carbide) in a hot discharge from a hollow cathode with various chlorinating reagents: copper monochloride, nickel chloride, magnesium chloride, for the purpose of accelerating their entrance into the excitation zone. It has been shown thermodynamically and experimentally that chlorination of metal zirconium and hafnium and their carbides with copper monochloride in hot hollow cathode conditions provides a sharp increase in the intensity of the lines of these elements

  20. Spatial and temporal variability of inorganic chlorine in Northwestern Europe

    Science.gov (United States)

    Sommariva, R.; Hollis, L. D. J.; Baker, A. R.; Ball, S. M.; Bell, T. G.; Cordell, R. L.; Fleming, Z.; Gaget, M.; Yang, M. X.; Monks, P. S.

    2015-12-01

    Chlorine is well known to be a strong oxidant in the atmosphere;chlorine reactivity impacts the formation of tropospheric ozone, theoxidation of methane and non-methane hydrocarbons, and the cycling ofnitrogen, sulphur and mercury. An accurate assessment of the roleplayed by chlorine in tropospheric chemical processes is complicatedby the scarce knowledge of its sources, sinks and distribution.We report observations of inorganic chlorine species (Cl2, ClNO2,particulate chloride) taken over the period 2014-2015 at threedifferent locations in Britain: an urban site a hundred kilometersfrom the ocean (Leicester), a coastal site mostly affected by shiptraffic (Penlee Point, Cornwall) and a coastal site experiencingeither clean air from the North Sea or polluted air from inland(Weybourne, Norfolk).This dataset provides a first look into the geographical distributionand seasonal variability of chlorine in Northwestern Europe: theresults suggest that, during the night, ClNO2 is ubiquitous withconcentrations in the range of hundreds to thousands of pptV at alllocations, whereas Cl2 can be observed only at coastal sites, withconcentrations of a few tens of pptV. The implications of thewidespread presence of these forms of inorganic chlorine for ozoneproduction and, in general, for the oxidative processes in the loweratmosphere are discussed with the help of a wide range of supportingmeasurements.

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

    Science.gov (United States)

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

    2014-05-01

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

  2. Theoretical Study on the Reaction of Chlorine Trifluoride Oxide with Propylene Oxide by Density Functional Theory%ClF3O和环氧丙烷反应的理论研究

    Institute of Scientific and Technical Information of China (English)

    闫华; 刘志勇; 史茂盛; 罗永锋; 颜澎; 贡雪东

    2015-01-01

    应用密度泛函理论对 ClF3 O 和环氧丙烷的反应机理进行了研究。在 B3PW91/6-31++G(d ,p )水平上优化了各驻点(反应物、中间体、过渡态和产物)的几何构型,并计算了它们的振动频率和零点振动能。采用 CCSD(T)/6-31++G(d ,p )//B3PW91/6-3l++G(d ,p )单点能计算方法求得各物质的能量,并做零点能校正。计算结果表明,ClF3 O 与 C3 H 6 O 可经过不同的反应路径,引发 C3 H 5 O 自由基和 ClOF2自由基生成环氧丙醇和三氟化氯,其中,位于 ClF3 O 周向位置的 F 原子与 C3 H 6 O 的 C(7)上与 CH 3异侧的 H(9)原子结合的活化能最低,仅15.63 kJ/mo1;ClF3 O 与 C3 H 6 O 反应生成的 C3 H 5 O 自由基和 ClOF2自由基继续反应,经过不同反应路径生成 C3 H 4 O、ClOF 和 HF,其中,ClOF2中的 F 原子和 C3 H 5 O 中的 H(2)或 H(4)原子结合是无能垒的过程。整个反应的主要路径为 C3 H 6 O+ClF3→O→TS12 P4(C3 H 5 O+HF+ClOF2→) P12(CH 2 CHCHO+2 HF+ClOF)。%Using density functional theory (DFT),the reaction of chlorine trifluoride oxide (ClF3 O)with propylene oxide (C3 H 6 O)was studied.At the B3PW91/6-31++G(d ,p )level,geometries of all species (re-actants,transition states and products)were optimized,and the vibrational frequencies and zero point vibration-al energies (ZPVE)were calculated.The energies of all species were refined with CCSD(T)/6-31++G(d,p)//B3PW91/6-31++G(d,p)method and ZPVE correction.The calculated results suggest that the initial reaction has various pathways to yield the main products of C3 H 5 O and ClOF2 radicals,and C3 H 6 O 2 and ClF3 mole-cules.The reactions of C3 H 5 O and ClOF2 radicals have different pathways to yield the main products of C3 H 4 O,ClOF and HF molecules.The main reaction channel is C3 H 6 O+ClF3→O→TS12 P4 (C3 H 5 O+HF+ClOF2→) P12 (CH 2 CHCHO+2 HF+ClOF).P4 is produced by C3 H 6 O and ClF3 O via TS12 with a low barrier of 1 5.63 kJ/mol,and P12 can be formed from P4 through a barrierless

  3. The chlorination of cooling water

    International Nuclear Information System (INIS)

    After reviewing the means of fighting biological pollution of cooling water circuits in nuclear power stations, the authors describe the chlorination treatment methods used by EDF. This deals with the massive shock chlorination of the cooling towers and the continuous low-level chlorination of coastal nuclear power stations. In both areas, the Research and Development Board of EDF has carried out and encouraged research with the aim of improving circuit protection, while still protecting the aquatic eco-system against damage that might be caused by waste chlorinated water

  4. Plant physiological response of strawberry fruit to chlorine dioxide gas treatment during postharvest storage

    Science.gov (United States)

    Chlorine dioxide, a strong oxidizing and sanitizing agent, is used as a postharvest sanitizer for fruits and vegetables and generally applied on a packing line using a chlorine dioxide generator. The objective of this research was to study the physiological responses of strawberries to ClO2 when app...

  5. Chlorination of calcium tungstate by mixture of chlorine and sulfur dioxide

    International Nuclear Information System (INIS)

    Results of thermodynamic calculations and experimental investigations of interaction of calcium tungstate with Cl2+SO2 mixture at 400-850 deg C are presented. It is shown that the processes passes through several sequential and parallel stages with formation of tungsten (6) oxide and calcium chloride as intermediate products. Peculiarities of the process are determined by the ratio of rates of WO3 formation and chlorination stages

  6. Detection, identification and formation of new iodinated disinfection byproducts in chlorinated saline wastewater effluents.

    Science.gov (United States)

    Gong, Tingting; Zhang, Xiangru

    2015-01-01

    The use of seawater for toilet flushing introduces high levels of inorganic ions, including iodide ions, into a city's wastewater treatment systems, resulting in saline wastewater effluents. Chlorination is widely used in disinfecting wastewater effluents owing to its low cost and high efficiency. During chlorination of saline wastewater effluents, iodide may be oxidized to hypoiodous acid, which may further react with effluent organic matter to form iodinated disinfection byproducts (DBPs). Iodinated DBPs show significantly higher toxicity than their brominated and chlorinated analogues and thus have been drawing increasing concerns. In this study, polar iodinated DBPs were detected in chlorinated saline wastewater effluents using a novel precursor ion scan method. The major polar iodinated DBPs were identified and quantified, and their organic precursors and formation pathways were investigated. The formation of iodinated DBPs under different chlorine doses and contact times was also studied. The results indicated that a few polar iodinated DBPs were generated in the chlorinated saline primary effluent, but few were generated in the chlorinated saline secondary effluent. Several major polar iodinated DBPs in the chlorinated saline primary effluent were proposed with structures, among which a new group of polar iodinated DBPs, iodo-trihydroxybenzenesulfonic acids, were identified and quantified. The organic precursors of this new group of DBPs were found to be 4-hydroxybenzenesulfonic acid and 1,2,3-trihydroxybenzene, and the formation pathways of these new DBPs were tentatively proposed. Both chlorine dose and contact time affected the formation of iodinated DBPs in the chlorinated saline wastewater effluents.

  7. Thermodynamic analysis of the selective chlorination of electric arc furnace dust.

    Science.gov (United States)

    Pickles, C A

    2009-07-30

    The remelting of automobile scrap in an electric arc furnace (EAF) results in the production of a dust, which contains high concentrations of the oxides of zinc, iron, calcium and other metals. Typically, the lead and zinc are of commercial value, while the other metals are not worth recovering. At the present time, EAF dusts are treated in high temperature Waelz rotary kiln-type processes, where the lead and zinc oxides are selectively reduced and simultaneously reoxidized and a crude zinc oxide is produced. Another alternative processing route is selective chlorination, in which the non-ferrous metals are preferentially chlorinated to their gaseous chlorides and in this manner separated from the iron. In the present research, a detailed thermodynamic analysis of this chlorination process has been performed and the following factors were investigated; temperature, amount of chlorine, lime content, silica content, presence of an inert gas and the oxygen potential. High lead and zinc recoveries as gaseous chlorides could be achieved but some of the iron oxide was also chlorinated. Additionally, the calcium oxide in the dust consumes chlorine, but this can be minimized by adding silica, which results in the formation of stable calcium silicates. The optimum conditions were determined for a typical dust composition. The selectivities achieved with chlorination were lower than those for reduction, as reported in the literature, but there are other advantages such as the potential recovery of copper.

  8. Thermodynamic analysis of the selective chlorination of electric arc furnace dust

    Energy Technology Data Exchange (ETDEWEB)

    Pickles, C.A., E-mail: pickles-c@mine.queensu.ca [Department of Mining Engineering, Queen' s University, Kingston, Ontario, K7L 3N6 (Canada)

    2009-07-30

    The remelting of automobile scrap in an electric arc furnace (EAF) results in the production of a dust, which contains high concentrations of the oxides of zinc, iron, calcium and other metals. Typically, the lead and zinc are of commercial value, while the other metals are not worth recovering. At the present time, EAF dusts are treated in high temperature Waelz rotary kiln-type processes, where the lead and zinc oxides are selectively reduced and simultaneously reoxidized and a crude zinc oxide is produced. Another alternative processing route is selective chlorination, in which the non-ferrous metals are preferentially chlorinated to their gaseous chlorides and in this manner separated from the iron. In the present research, a detailed thermodynamic analysis of this chlorination process has been performed and the following factors were investigated; temperature, amount of chlorine, lime content, silica content, presence of an inert gas and the oxygen potential. High lead and zinc recoveries as gaseous chlorides could be achieved but some of the iron oxide was also chlorinated. Additionally, the calcium oxide in the dust consumes chlorine, but this can be minimized by adding silica, which results in the formation of stable calcium silicates. The optimum conditions were determined for a typical dust composition. The selectivities achieved with chlorination were lower than those for reduction, as reported in the literature, but there are other advantages such as the potential recovery of copper.

  9. Photostability of different chlorine photosensitizers

    International Nuclear Information System (INIS)

    In this paper, we report the photodegradation of three different chlorine photosensitizers (Photoditazine®, Radachlorin®, and Foscan®). The photosensitizer degradation was analyzed by changes in the fluorescence spectrum during illumination. The rate of fluorescence variation was normalized to the solution absorption and the photon energy resulting in the determination of the necessary number of photons to be absorbed to induce photosensitizer photodegradation. The parameter for rate of the molecules decay, the photon fluence rate and optical properties of the solution allow us to determine the photosensitizer stability in solution during illumination. The results show that the order of susceptibility for photodegradation rate is: Radachlorin® < Photoditazine® < Foscan®. This difference in the photodegradation rate for Foscan can be explained by the high proportion of aggregates in solution that inhibit the photo-oxidative process that impede the singlet oxygen formation. We hypothesize that there is a correlation between photodegradation rate and photodynamic efficacy witch is governed by the singlet oxygen formation responsible for the most relevant reaction of the cell death photodynamic induction. Then its is important to know the photostability of different types of drugs since the photodegradation rate, the photodegradation as well as the photodynamic efficacy are strong correlated to the oxygen concentration in the tissue

  10. Chlorination of tramadol: Reaction kinetics, mechanism and genotoxicity evaluation.

    Science.gov (United States)

    Cheng, Hanyang; Song, Dean; Chang, Yangyang; Liu, Huijuan; Qu, Jiuhui

    2015-12-01

    Tramadol (TRA) is one of the most detected analgesics in environmental matrices, and it is of high significance to study the reactivity of TRA during chlorination considering its potential toxicity to the environment. The chlorine/TRA reaction is first order with respect to the TRA concentration, and a combination of first-order and second-order with respect to chlorine concentration. The pH dependence of the observed rate constants (kobs) showed that the TRA oxidation reactivity increased with increasing pH. kobs can be quantitatively described by considering all active species including Cl2, Cl2O and HOCl, and the individual rate constants of HOCl/TRA(0), HOCl/TRAH(+), Cl2/TRA and Cl2O/TRA reactions were calculated to be (2.61±0.29)×10(3)M(-1)s(-1), 14.73±4.17M(-1)s(-1), (3.93±0.34)×10(5)M(-1)s(-1) and (5.66±1.83)×10(6)M(-1)s(-1), respectively. Eleven degradation products were detected with UPLC-Q-TOF-MS, and the corresponding structures of eight products found under various pH conditions were proposed. The amine group was proposed to be the initial attack site under alkaline pH conditions, where reaction of the deprotonated amine group with HOCl is favorable. Under acidic and neutral pH conditions, however, two possible reaction pathways were proposed. One is an electrophilic substitution on the aromatic ring, and another is an electrophilic substitution on the nitrogen, leading to an N-chlorinated intermediate, which can be further oxidized. Finally, the SOS/umu test showed that the genotoxicity of TRA chlorination products increased with increasing dosage of chlorine, which was mostly attributed to the formation of some chlorine substitution products.

  11. Aluminum recovery from coal fly ash by high temperature chlorination

    Energy Technology Data Exchange (ETDEWEB)

    Wijatno, H.

    1977-10-01

    A study of aluminum recovery from power plant fly ash by high temperature chlorination was undertaken to demonstrate that fly ash could be a potential source of aluminum, iron and possibly silicon. Magnetic separation of the iron oxide served as a first step to alleviate the iron contamination problem. However, the agglomeration of some iron oxide with alumina and silica made it difficult to completely separate the iron from the fly ash. Further iron separation was achieved by chlorinating the nonmagnetic ash fraction at 550/sup 0/C for 30 minutes. This reduced the iron oxide content to less than 4 percent by weight. Chlorine flow rates affected the reaction rate much more drastically than temperatures. This suggested that diffusion was the major rate-controlling step. Besides Fe/sub 2/O/sub 3/, Al/sub 2/O/sub 3/ and SiO/sub 2/, other oxides such as CaO, K/sub 2/O, Na/sub 2/O and MgO might have complicated the alumina recovery by forming individual chlorides or complexes. Investigating methods for separating more Fe/sub 2/O/sub 3/, and possibly CaO, K/sub 2/O, Na/sub 2/O and MgO from the nonmagnetic ash fraction before chlorinating it is highly recommended.

  12. The effect of chlorine dioxide on polymeric packaging materials

    Science.gov (United States)

    Chlorine dioxide (ClO2), with its high oxidizing capacity and broad disinfecting property, is used frequently as a disinfectant in many applications. As a biocide in food applications, it showed a microbial inactivating capacity against many important pathogenic and spoilage microorganisms, located ...

  13. ASCORBIC ACID REDUCTION OF ACTIVE CHLORINE PRIOR TO DETERMINING AMES MUTAGENICITY OF CHLORINATED NATURAL ORGANIC MATTER (NOM)

    Science.gov (United States)

    Many potable water disinfection byproducts (DBPs) that result from the reaction of natural organic matter (NOM) with oxidizing chlorine are known or suspected to be carcinogenic and mutagenic. The Ames assay is routinely used to assess an overall level of mutagenicity for all com...

  14. A carbon nanotube based resettable sensor for measuring free chlorine in drinking water

    Energy Technology Data Exchange (ETDEWEB)

    Hsu, Leo H. H. [School of Biomedical Engineering, McMaster University, Hamilton L8S 4L8 (Canada); Hoque, Enamul; Kruse, Peter [Department of Chemistry and Chemical Biology, McMaster University, Hamilton L8S 4L8 (Canada); Ravi Selvaganapathy, P. [School of Biomedical Engineering, McMaster University, Hamilton L8S 4L8 (Canada); Department of Mechanical Engineering, McMaster University, Hamilton L8S 4L7 (Canada)

    2015-02-09

    Free chlorine from dissolved chlorine gas is widely used as a disinfectant for drinking water. The residual chlorine concentration has to be continuously monitored and accurately controlled in a certain range around 0.5–2 mg/l to ensure drinking water safety and quality. However, simple, reliable, and reagent free monitoring devices are currently not available. Here, we present a free chlorine sensor that uses oxidation of a phenyl-capped aniline tetramer (PCAT) to dope single wall carbon nanotubes (SWCNTs) and to change their resistance. The oxidation of PCAT by chlorine switches the PCAT-SWCNT system into a low resistance (p-doped) state which can be detected by probing it with a small voltage. The change in resistance is found to be proportional to the log-scale concentration of the free chlorine in the sample. The p-doping of the PCAT-SWCNT film then can be electrochemically reversed by polarizing it cathodically. This sensor not only shows good sensing response in the whole concentration range of free chlorine in drinking water but is also able to be electrochemically reset back many times without the use of any reagents. This simple sensor is ideally suited for measuring free chlorine in drinking water continuously.

  15. Grundfoss: Chlorination of Swimming Pools

    DEFF Research Database (Denmark)

    Hjorth, Poul G.; Hogan, John; Andreassen, Viggo

    1998-01-01

    Grundfos asked for a model, describing the problem of mixing chemicals, being dosed into water systems, to be developed. The application of the model should be dedicated to dosing aqueous solution of chlorine into swimming pools.......Grundfos asked for a model, describing the problem of mixing chemicals, being dosed into water systems, to be developed. The application of the model should be dedicated to dosing aqueous solution of chlorine into swimming pools....

  16. Research on the Preparation of Crosslinked Starch Chlorinated with Sodium Hypochlorite

    Institute of Scientific and Technical Information of China (English)

    LiangYin; ZhuZhi-feng

    2003-01-01

    Optimization of reaction variables such as catalyst type and amount, reaction temperature and time, formaldehyde amount, and oxidation extent of starch was studied for the crosslinking reaction of chlorinated cornstarch with form-aldehyde. The reaction was carried out in aqueous suspension dispersed granular chlorinated cornstarch. Catalysts such as hydrochloric acid, sulfuric acid, and nitric acid were individually evaluated. The results show that the type and amount of the inorganic acid, formaldehyde amount, and oxidation extent of the chlorinated starch strongly affect the reaction efficiency. Hydrochloric acid shows the best catalyst effect on the reaction. Increasing the amount of the catalyst favourably raises the reaction efficiency. It is also demonstrated that the reaction efficiency is enhanced with the decrease of the oxidation extent of granular chlorinated starch.

  17. Research on the Preparation of Crosslinked Starch Chlorinated with Sodium Hypochlorite

    Institute of Scientific and Technical Information of China (English)

    Liang Yin; Zhu Zhi-feng

    2003-01-01

    Optimization of reaction variables such as catalyst type and amount, reaction temperature and time, formaldehyde amount, and oxidation extent of starch was studied for the crosslinking reaction of chlorinated cornstarch with formaldehyde. The reaction was carried out in aqueous suspension dispersed granular chlorinated cornstarch. Catalysts such as hydrochloric acid, sulfuric acid, and nitric acid were individually evaluated. The results show that the type and amount of the inorganic acid, formaldehyde amount, and oxidation extent of the chlorinated starch strongly affect the reaction efficiency. Hydrochloric acid shows the best catalyst effect on the reaction. Increasing the amount of the catalyst favourably raises the reaction efficiency. It is also demonstrated that the reaction efficiency is enhanced with the decrease of the oxidation extent of granular chlorinated starch.

  18. EFFECTS OF OZONE, CHLORINE DIOXIDE, CHLORINE, AND MONOCHLORAMINE ON CRYTOSPORIDIUM PARVUM OOCYST VIABILITY

    Science.gov (United States)

    Purified Cryptosporiodium parvum oocysts were exposed to ozone, chlorine dioxide, chlorine, and monochloramine. Excystation and mouse infectivity were compareatively evaluated to assess oocyst viability. Ozone and chlorine dioxide more effectively inactivated oocysts than chlor...

  19. Synthesis of magnesium aluminate spinel by periclase and alumina chlorination

    Energy Technology Data Exchange (ETDEWEB)

    Orosco, Pablo, E-mail: porosco@unsl.edu.ar [Instituto de Investigaciones en Tecnología Química (INTEQUI), Chacabuco y Pedernera, San Luis (Argentina); Facultad de Química, Bioquímica y Farmacia, Universidad Nacional de San Luis Chacabuco y Pedernera, San Luis (Argentina); Barbosa, Lucía [Instituto de Investigaciones en Tecnología Química (INTEQUI), Chacabuco y Pedernera, San Luis (Argentina); Instituto de Ciencias Básicas (ICB), Universidad Nacional de Cuyo Parque General San Martín, Mendoza (Argentina); Ruiz, María del Carmen [Instituto de Investigaciones en Tecnología Química (INTEQUI), Chacabuco y Pedernera, San Luis (Argentina); Facultad de Química, Bioquímica y Farmacia, Universidad Nacional de San Luis Chacabuco y Pedernera, San Luis (Argentina)

    2014-11-15

    Highlights: • Use of chlorination for the synthesis of magnesium aluminate spinel. • The reagents used were alumina, periclase and chlorine. • Isothermal and non-isothermal assays were performed in air and Cl{sub 2}–N{sub 2} flows. • The chlorination produced magnesium aluminate spinel at 700 °C. • Selectivity of the chlorination reaction to obtain spinel is very high. - Abstract: A pyrometallurgical route for the synthesis of magnesium aluminate spinel by thermal treatment of a mechanical mixture containing 29 wt% MgO (periclase) and 71 wt% Al{sub 2}O{sub 3} (alumina) in chlorine atmosphere was developed and the results were compared with those obtained by calcining the same mixture of oxides in air atmosphere. Isothermal and non-isothermal assays were performed in an experimental piece of equipment adapted to work in corrosive atmospheres. Both reagents and products were analyzed by differential thermal analysis (DTA), X-ray diffraction (XRD) and X-ray fluorescence (XRF). Thermal treatment in Cl{sub 2} atmosphere of the MgO–Al{sub 2}O{sub 3} mixture produces magnesium aluminate spinel at 700 °C, while in air, magnesium spinel is generated at 930 °C. The synthesis reaction of magnesium aluminate spinel was complete at 800 °C.

  20. Synthesis of magnesium aluminate spinel by periclase and alumina chlorination

    International Nuclear Information System (INIS)

    Highlights: • Use of chlorination for the synthesis of magnesium aluminate spinel. • The reagents used were alumina, periclase and chlorine. • Isothermal and non-isothermal assays were performed in air and Cl2–N2 flows. • The chlorination produced magnesium aluminate spinel at 700 °C. • Selectivity of the chlorination reaction to obtain spinel is very high. - Abstract: A pyrometallurgical route for the synthesis of magnesium aluminate spinel by thermal treatment of a mechanical mixture containing 29 wt% MgO (periclase) and 71 wt% Al2O3 (alumina) in chlorine atmosphere was developed and the results were compared with those obtained by calcining the same mixture of oxides in air atmosphere. Isothermal and non-isothermal assays were performed in an experimental piece of equipment adapted to work in corrosive atmospheres. Both reagents and products were analyzed by differential thermal analysis (DTA), X-ray diffraction (XRD) and X-ray fluorescence (XRF). Thermal treatment in Cl2 atmosphere of the MgO–Al2O3 mixture produces magnesium aluminate spinel at 700 °C, while in air, magnesium spinel is generated at 930 °C. The synthesis reaction of magnesium aluminate spinel was complete at 800 °C

  1. Coagulation properties of anelectrochemically prepared polyaluminum chloride containing active chlorine

    Institute of Scientific and Technical Information of China (English)

    HU Chengzhi; LIU Huijuan; QU Jiuhui

    2006-01-01

    With high content of the Al13 species and the active chloride, an electrochemically prepared polyaluminum chloride (E-PACl) presents integrated efficiency of coagulation and oxidation. The coagulation properties of E-PACl were systemically investigated through jar tests in the various water quality conditions. The active chlorine in E-PACl can significantly influence the coagulation behavior due to the active chlorine preoxidation, which can change the surface charge characteristic of organic matter (OM) in water. The active chlorine preoxidation could improve the E-PACl coagulation efficiency if the water possessed the characteristics of relatively low OM content (2 mg/L) and high hardness (278 mg CaCO3/L). In the water with medium content of OM (5 mg/L), dosage would be a crucial factor to decide whether the active chlorine in E-PACl aided coagulation process or not. Comparing with alkaline condition, active chlorine would show a more significant influence on the coagulation process in acidic region.

  2. Degradation of atrazine by UV/chlorine: Efficiency, influencing factors, and products.

    Science.gov (United States)

    Kong, Xiujuan; Jiang, Jin; Ma, Jun; Yang, Yi; Liu, Weili; Liu, Yulei

    2016-03-01

    In this work, the degradation of atrazine by the combination of UV and chlorine (UV/chlorine) due to the formation of radicals during chlorine photolysis was systematically investigated in terms of efficiency, factors that influence the degradation kinetics, as well as oxidation products. It was found that the degradation efficiency of atrazine was enhanced by UV/chlorine compared to UV or chlorine alone. The degradation efficiency of atrazine was favorable at a lower pH, but was inhibited in the presence of natural organic matters. Meanwhile, the initial chlorine dosage, alkalinity, and chloride barely influenced the degradation efficiency under neutral pH conditions. The degradation of atrazine by UV/chlorine was inhibited in real waters (i.e., surface water and ground water) compared to in deionized water but was still more effective than UV alone. The oxidation products of atrazine resulting from de-alkylation, dechlorination-hydroxylation, alkylic-hydroxylation, alkylic-oxidation, alkylic-hydroxylation-dehydration, deamination-hydroxylation, and dechlorination-hydrogenation in UV/chlorine process were detected, which were slightly different from those formed in UV/H2O2 (commonly used UV-based advanced oxidation process). Particularly, the yields of three primary transformation products (desethyl-atrazine (DEA), desisopropyl-atrazine (DIA), and desethyl-desisopropyl-atrazine (DEIA)) were comparatively quantified in these two processes. The different trend of them formed in UV/chlorine system (DEA:DIA≈4) compared to that formed in UV/H2O2 system (DEA:DIA≈1) could be ascribed to the different reaction reactivities and mechanisms between HO• and Cl• with atrazine.

  3. Transformation pathways and acute toxicity variation of 4-hydroxyl benzophenone in chlorination disinfection process.

    Science.gov (United States)

    Liu, Wei; Wei, Dongbin; Liu, Qi; Du, Yuguo

    2016-07-01

    Benzophenones compounds (BPs) are widely used as UV filters, and have been frequently found in multiple environmental matrices. The residual of BPs in water would cause potential threats on ecological safety and human health. Chlorination disinfection is necessary in water treatment process, in which many chemicals remained in water would react with disinfectant chlorine and form toxic by-products. By using ultra performance liquid phase chromatography quadrupole time of flight mass spectrometer (UPLC-QTOF-MS), nuclear magnetic resonance (NMR), the transformation of 4-hydroxyl benezophenone (4HB) with free available chlorine (FAC) was characterized. Eight major products were detected and seven of them were identified. Transformation pathways of 4HB under acid, neutral, and alkaline conditions were proposed respectively. The transformation mechanisms involved electrophilic chlorine substitution of 4HB, Baeyer-Villiger oxidation of ketones, hydrolysis of esters and oxidative breakage of benzene ring. The orthogonal experiments of pH and dosages of disinfectant chlorine were conducted. The results suggested that pH conditions determined the occurrence of reaction types, and the dosages of disinfectant chlorine affected the extent of reactions. Photobacterium assay demonstrated that acute toxicity had significant increase after chlorination disinfection of 4HB. It was proved that 3,5-dichloro-4HB, one of the major transformation products, was responsible for the increasing acute toxicity after chlorination. It is notable that, 4HB at low level in real ambient water matrices could be transformed during simulated chlorination disinfection practice. Especially, two major products 3-chloro-4HB and 3,5-dichloro-4HB were detected out, implying the potential ecological risk after chlorination disinfection of 4HB.

  4. Transformation pathways and acute toxicity variation of 4-hydroxyl benzophenone in chlorination disinfection process.

    Science.gov (United States)

    Liu, Wei; Wei, Dongbin; Liu, Qi; Du, Yuguo

    2016-07-01

    Benzophenones compounds (BPs) are widely used as UV filters, and have been frequently found in multiple environmental matrices. The residual of BPs in water would cause potential threats on ecological safety and human health. Chlorination disinfection is necessary in water treatment process, in which many chemicals remained in water would react with disinfectant chlorine and form toxic by-products. By using ultra performance liquid phase chromatography quadrupole time of flight mass spectrometer (UPLC-QTOF-MS), nuclear magnetic resonance (NMR), the transformation of 4-hydroxyl benezophenone (4HB) with free available chlorine (FAC) was characterized. Eight major products were detected and seven of them were identified. Transformation pathways of 4HB under acid, neutral, and alkaline conditions were proposed respectively. The transformation mechanisms involved electrophilic chlorine substitution of 4HB, Baeyer-Villiger oxidation of ketones, hydrolysis of esters and oxidative breakage of benzene ring. The orthogonal experiments of pH and dosages of disinfectant chlorine were conducted. The results suggested that pH conditions determined the occurrence of reaction types, and the dosages of disinfectant chlorine affected the extent of reactions. Photobacterium assay demonstrated that acute toxicity had significant increase after chlorination disinfection of 4HB. It was proved that 3,5-dichloro-4HB, one of the major transformation products, was responsible for the increasing acute toxicity after chlorination. It is notable that, 4HB at low level in real ambient water matrices could be transformed during simulated chlorination disinfection practice. Especially, two major products 3-chloro-4HB and 3,5-dichloro-4HB were detected out, implying the potential ecological risk after chlorination disinfection of 4HB. PMID:27085063

  5. Effects of assimilable organic carbon and free chlorine on bacterial growth in drinking water.

    Directory of Open Access Journals (Sweden)

    Xiaolu Liu

    Full Text Available Assimilable organic carbon (AOC is one of the most important factors affecting the re-growth of microorganisms in drinking water. High AOC concentrations result in biological instability, but disinfection kills microbes to ensure the safety of drinking water. Free chlorine is an important oxidizing agent used during the disinfection process. Therefore, we explored the combined effects of AOC and free chlorine on bacterial growth in drinking water using flow cytometry (FCM. The initial AOC concentration was 168 μg.L(-1 in all water samples. Without free chlorine, the concentrations of intact bacteria increased but the level of AOC decreased. The addition of sodium hypochlorite caused an increase and fluctuation in AOC due to the oxidation of organic carbon. The concentrations of intact bacteria decreased from 1.1 × 10(5 cells.mL(-1 to 2.6 × 10(4 cells.mL(-1 at an initial free chlorine dose of 0.6 mg.L(-1 to 4.8 × 10(4 cells.mL(-1 at an initial free chlorine dose of 0.3 mg.L(-1 due to free chlorine originating from sodium hypochlorite. Additionally, free chlorine might be more obviously affected AOC concentrations than microbial growth did. These results suggested that AOC and free chlorine might have combined effects on microbial growth. In this study, our results showed concentrations determined by FCM were higher than those by HPC, which indicated that some E. coli detected by FCM might not be detected using HPC in drinking water. The level of free chlorine might restrain the consumption of AOC by inhibiting the growth of E. coli; on the other hand, chlorination might increase the level of AOC, thereby increase the potential for microbial growth in the drinking water network.

  6. Metals releases and disinfection byproduct formation in domestic wells following shock chlorination

    Directory of Open Access Journals (Sweden)

    M. Walker

    2010-06-01

    Full Text Available Shock chlorination is used for rapid disinfection to control pathogens and nuisance bacteria in domestic wells. A typical shock chlorination procedure involves adding sodium hypochlorite in liquid bleach solutions to achieve concentrations of free chlorine of up to 200 ppm in the standing water of a well. The change in pH and oxidation potential may bring trace metals from aquifer materials into solution and chlorine may react with dissolved organic carbon to form disinfection byproducts. We carried out experiments with four wells to observe and determine the persistence of increased concentrations of metals and disinfection byproducts. Water samples from shock chlorinated wells were analyzed for Pb, Cu, As, radionuclides and disinfection byproducts (haloacetic acids and trihalomethanes, immediately prior to treatment, after sufficient contact time with chlorine had elapsed, and at intervals determined by the number of casing volumes purged, for up to four times the well casing volume.

    Elevated concentrations of lead and copper dissipated in proportion to free chlorine (measured semi-quantitatively during the purging process. Trihalomethanes and haloacetic acids were formed in wells during disinfection. In one of two wells tested, disinfection byproducts dissipated in proportion to free chlorine during purging. However, one well retained disinfection byproducts and free chlorine after four well volumes had been purged. Although metals returned to background concentrations in this well, disinfection byproducts remained elevated, though below the MCL, likely because purging volume was insufficient. Simple chlorine test strips may be a useful method for indicating when purging is adequate to remove metals and disinfection by-products mobilized and formed by shock chlorination.

  7. Metals releases and disinfection byproduct formation in domestic wells following shock chlorination

    Directory of Open Access Journals (Sweden)

    M. Walker

    2011-01-01

    Full Text Available Shock chlorination is used for rapid disinfection to control pathogens and nuisance bacteria in domestic wells. A typical shock chlorination procedure involves adding sodium hypochlorite in liquid bleach solutions to achieve concentrations of free chlorine of up to 200 mg L−1 in the standing water of a well. The change in pH and oxidation potential may bring trace metals from aquifer materials into solution and chlorine may react with dissolved organic carbon to form disinfection byproducts. We carried out experiments with four wells to observe and determine the persistence of increased concentrations of metals and disinfection byproducts. Water samples from shock chlorinated wells were analyzed for Pb, Cu, As, radionuclides and disinfection byproducts (haloacetic acids and trihalomethanes, immediately prior to treatment, after sufficient treatment time with chlorine had elapsed, and at intervals determined by the number of casing volumes purged, for up to four times the well casing volume.

    Elevated concentrations of lead and copper dissipated in proportion to free chlorine (measured semi-quantitatively during the purging process. Trihalomethanes and haloacetic acids were formed in wells during disinfection. In one of two wells tested, disinfection byproducts dissipated in proportion to free chlorine during purging. However, one well retained disinfection byproducts and free chlorine after 4 WV had been purged. Although metals returned to background concentrations in this well, disinfection byproducts remained elevated, though below the MCL. This may have been due to well construction characteristics and interactions with aquifer materials. Simple chlorine test strips may be a useful method for indicating when purging is adequate to remove metals and disinfection by-products mobilized and formed by shock chlorination.

  8. Chlorine/UV Process for Decomposition and Detoxification of Microcystin-LR.

    Science.gov (United States)

    Zhang, Xinran; Li, Jing; Yang, Jer-Yen; Wood, Karl V; Rothwell, Arlene P; Li, Weiguang; Blatchley Iii, Ernest R

    2016-07-19

    Microcystin-LR (MC-LR) is a potent hepatotoxin that is often associated with blooms of cyanobacteria. Experiments were conducted to evaluate the efficiency of the chlorine/UV process for MC-LR decomposition and detoxification. Chlorinated MC-LR was observed to be more photoactive than MC-LR. LC/MS analyses confirmed that the arginine moiety represented an important reaction site within the MC-LR molecule for conditions of chlorination below the chlorine demand of the molecule. Prechlorination activated MC-LR toward UV254 exposure by increasing the product of the molar absorption coefficient and the quantum yield of chloro-MC-LR, relative to the unchlorinated molecule. This mechanism of decay is fundamentally different than the conventional view of chlorine/UV as an advanced oxidation process. A toxicity assay based on human liver cells indicated MC-LR degradation byproducts in the chlorine/UV process possessed less cytotoxicity than those that resulted from chlorination or UV254 irradiation applied separately. MC-LR decomposition and detoxification in this combined process were more effective at pH 8.5 than at pH 7.5 or 6.5. These results suggest that the chlorine/UV process could represent an effective strategy for control of microcystins and their associated toxicity in drinking water supplies. PMID:27338715

  9. Laboratory tests using chlorine trifluoride in support of deposit removal at MSRE

    International Nuclear Information System (INIS)

    Experimental trials were conducted to investigate some unresolved issues regarding the use of chlorine trifluoride (ClF3) for removal of uranium-bearing deposits in the Molten Salt Reactor Experiment (MSRE) off-gas system. The safety and effectiveness of operation of the fixed-bed trapping system for removal of reactive gases were the primary focus. The chief uncertainty concerns the fate of chlorine in the system and the potential for forming explosive chlorine oxides (primarily chlorine dioxide) in the trapping operation. Tests at the MSRE Reactive Gas Removal System reference conditions and at conditions of low ClF3 flow showed that only very minor quantities of reactive halogen oxides were produced before column breakthrough. Somewhat larger quantities accompanied breakthrough. A separation test that exposed irradiated MSRE simulant salt to ClF3 confirmed the expectation that the salt is basically inert for brief exposures to ClF3 at room temperature

  10. Laboratory tests using chlorine trifluoride in support of deposit removal at MSRE

    Energy Technology Data Exchange (ETDEWEB)

    Williams, D.F.; Rudolph, J.C.; Del Cul, G.D.; Loghry, S.L.; Simmons, D.W.; Toth, L.M.

    1997-04-01

    Experimental trials were conducted to investigate some unresolved issues regarding the use of chlorine trifluoride (ClF{sub 3}) for removal of uranium-bearing deposits in the Molten Salt Reactor Experiment (MSRE) off-gas system. The safety and effectiveness of operation of the fixed-bed trapping system for removal of reactive gases were the primary focus. The chief uncertainty concerns the fate of chlorine in the system and the potential for forming explosive chlorine oxides (primarily chlorine dioxide) in the trapping operation. Tests at the MSRE Reactive Gas Removal System reference conditions and at conditions of low ClF{sub 3} flow showed that only very minor quantities of reactive halogen oxides were produced before column breakthrough. Somewhat larger quantities accompanied breakthrough. A separation test that exposed irradiated MSRE simulant salt to ClF{sub 3} confirmed the expectation that the salt is basically inert for brief exposures to ClF{sub 3} at room temperature.

  11. Enhanced Elemental Mercury Removal from Coal-fired Flue Gas by Sulfur-chlorine Compounds

    OpenAIRE

    Miller, Nai-Qiang Yan-Zan Qu Yao Chi Shao-Hua Qiao Ray Dod Shih-Ger Chang Charles

    2008-01-01

    Oxidation of Hg0 with any oxidant or converting it to a particle-bound form can facilitate its removal. Two sulfur-chlorine compounds, sulfur dichloride (SCl2) and sulfur monochloride (S2Cl2), were investigated as oxidants for Hg0 by gas phase reaction and by surface-involved reactions in the presence of flyash or activated carbon. The gas phase reaction rate constants between Hg0 and the sulfur/chlorine compounds were determined, and the effects of temperature and the main components in flue...

  12. Effects of ozone, chlorine dioxide, chlorine, and monochloramine on Cryptosporidium parvum oocyst viability.

    OpenAIRE

    Korich, D G; Mead, J R; Madore, M S; Sinclair, N. A.; Sterling, C R

    1990-01-01

    Purified Cryptosporidium parvum oocysts were exposed to ozone, chlorine dioxide, chlorine, and monochloramine. Excystation and mouse infectivity were comparatively evaluated to assess oocyst viability. Ozone and chlorine dioxide more effectively inactivated oocysts than chlorine and monochloramine did. Greater than 90% inactivation as measured by infectivity was achieved by treating oocysts with 1 ppm of ozone (1 mg/liter) for 5 min. Exposure to 1.3 ppm of chlorine dioxide yielded 90% inactiv...

  13. Formation of disinfection byproducts upon chlorine dioxide preoxidation followed by chlorination or chloramination of natural organic matter.

    Science.gov (United States)

    Yang, Xin; Guo, Wanhong; Lee, Wontae

    2013-06-01

    Chlorine dioxide (ClO2) is often used as an oxidant to remove taste, odor and color during water treatment. Due to the concerns of the chlorite formation, chlorination or chloramination is often applied after ClO2 preoxidation. We investigated the formation of regulated and emerging disinfection byproducts (DBPs) in sequential ClO2-chlorination and ClO2-chloramination processes. To clarify the relationship between the formation of DBPs and the characteristics of natural organic matter (NOM), changes in the properties of NOM before and after ClO2 oxidation were characterized by fluorescence, Fourier transform infrared spectroscopy (FTIR), and size and resin fractionation techniques. ClO2 preoxidation destroyed the aromatic and conjugated structures of NOM and transformed large aromatic and long aliphatic chain organics to small and hydrophilic organics. Treatment with ClO2 alone did not produce significant amount of trihalomethanes (THMs) and haloacetic acids (HAAs), but produced chlorite. ClO2 preoxidation reduced THMs, HAAs, haloacetonitriles (HANs) and chloral hydrate (CH) during subsequent chlorination, but no reduction of THMs was observed during chloramination. Increasing ClO2 doses enhanced the reduction of most DBPs except halonitromethanes (HNMs) and haloketones (HKs). The presence of bromide increased the formation of total amount of DBPs and also shifted DBPs to more brominated ones. Bromine incorporation was higher in ClO2 treated samples. The results indicated that ClO2 preoxidation prior to chlorination is applicable for control of THM, HAA and HAN in both pristine and polluted waters, but chlorite formation is a concern and HNMs and HKs are not effectively controlled by ClO2 preoxidation.

  14. Reaction products from the chlorination of seawater. Final report 15 Jul 75-14 Jul 80

    Energy Technology Data Exchange (ETDEWEB)

    Carpenter, J.H.; Smith, C.A.; Zika, R.G.

    1981-03-01

    Chemical treatment of natural waters, in particular the use of chlorine as a biocide, modifies the chemistry of these waters in ways that are not fully understood. The research described in this report examined both inorganic and organic reaction products from the chlorination of seawater using a variety of analytical approaches. Some analytical methods in widespread current use underestimate the residual oxidants in chlorinated seawater by as much as 70% depending upon the detail of the procedures. The chlorination of seawater in the presence of light produces substantial quantities of bromate ions which can influence standard analytical procedures and represents an unknown factor in estuarine and coastal waters. The copper complexing capacity of Biscayne Bay, Florida water was found to be substantially reduced with the addition of chlorine. Analysis was made by anodic stripping voltammetry on water samples after successive additions of copper sulfate solution. Laboratory chlorination of water from the intake of the Port Everglades, Florida power plant produces bromoform levels comparable to that found in the plant discharge. These results are in contrast to results reported in the literature for a power plant on the Patuxent estuary in Maryland, so that bromoform production appears to be site-specific. Chloroform extracts of chlorinated Biscayne Bay water are found to contain halogenated compounds which are new and different, and which pose unusual analytical problems. Studies using GC/ECD, GC/MS, HPLC, H NMR, differential pulsed polarography and other techniques on natural extracts and synthesized compounds are reported.

  15. Pilot-scale study of removal effect on Chironomid larvae with chlorine dioxide

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Chironomid larvae propagated excessively in eutrophic water body and could not be effectively inactivated by the conventional disinfection process like chlorination due to its stronger resistance to oxidation. In this paper, a pilot-scale study of chlorine dioxide preoxidation cooperating with routine clarification process for Chironomid larvae removal was conducted in Shenzhen Waterworks in Guangdong Province, China. The experimental results were compared with that of the existing prechlorination process in several aspects, including the Chironomid larvae removal efficiencies of water samples taken from the outlets of sedimentation tank, sand filter, the security of drinking water and so on. The results showed that chlorine dioxide might be more effective to inactivate Chironomid larvae than chlorine and Chironomid larvae could be thoroughly removed from water by pre-dosing chlorine dioxide process. The GC-MS examination and Ames test further showed that the sort and amount of organic substance in the treated water by chlorine dioxide preoxidation were evidently less than that ofprechlorination and the mutagenicity of drinking water treated by pre-dosing chlorine dioxide was substantially reduced compared with prechlorination.

  16. Full-scale study of removal effect on Cyclops of zooplankton with chlorine dioxide

    Institute of Scientific and Technical Information of China (English)

    LIN Tao; CUI Fu-yi; LIU Dong-mei; AN Dong

    2004-01-01

    Cyclops of zooplankton propagated excessively in eutrophic water body and could not be effectively inactivated by the conventional disinfections process like chlorination due to its stronger resistance to oxidation. In this paper, a full-scale study of chlorine dioxide preoxidation cooperating with routine clarification process for Cyclops removal was conducted in a waterworks. The experimental results were compared with that of the existing prechlorination process in several aspects: including the Cyclops removal efficiencies of water samples taken from the outlets of sedimentation tank and sand filter and the security of drinking water etc. The results showed that chlorine dioxide might be more effective to inactivate Cyclops than chlorine and Cyclops could be thoroughly removed from water by pre-dosing chlorine dioxide process. The GC-MS examination and Ames test further showed that the sort and amount of organic substance in the treated water by chlorine dioxide preoxidation were evidently less than that of prechlorination and the mutagenicity of drinking water treated by pre-dosing chlorine dioxide was substantially reduced compared with prechlorination.

  17. Ultrafast measurements of chlorine dioxide photochemistry

    Energy Technology Data Exchange (ETDEWEB)

    Ludowise, P.D.

    1997-08-01

    Time-resolved mass spectrometry and time-resolved photoelectron spectroscopy are used to study the ultrafast photodissociation dynamics of chlorine dioxide, an important constituent in stratospheric ozone depletion. Chapter 1 introduces these pump/probe techniques, in which a femtosecond pump pulse excites a molecule to a dissociative state. At a later time, a second femtosecond probe pulse ionizes the molecule. The resulting mass and photoelectron spectra are acquired as a function of the delay between the pump and probe pulses, which follows the evolution of the molecule on the excited state. A comparison to other techniques used to study reaction dynamics is discussed. Chapter 2 includes a detailed description of the design and construction of the experimental apparatus, which consists of a femtosecond laser system, a molecular beam time-of-flight spectrometer, and a data acquisition system. The time-of-flight spectrometer is specifically designed to have a short flight distance to maximize the photoelectron collection efficiency without degrading the resolution, which is limited by the bandwidth of the femtosecond laser system. Typical performance of the apparatus is demonstrated in a study of the time-resolved photoelectron spectroscopy of nitric oxide. The results of the time-resolved mass spectrometry experiments of chlorine dioxide are presented in Chapter 3. Upon excitation to the A {sup 2}A{sub 2} state near 3.2 eV, the molecule dissociates through an indirect two-step mechanism. The direct dissociation channel has been predicted to be open, but is not observed. A quantum beat is observed in the OClO{sup +} species, which is described as a vibrational coherence of the optically prepared A {sup 2}A{sub 2} state. Chapter 4 presents the results of the time-resolved photoelectron experiments of chlorine dioxide. At short delay time, the quantum beat of the OClO{sup +} species is observed in the X {sup 1}A{sub 1} state of the ion. At infinite delay, the signal

  18. Chlorine signal attenuation in concrete.

    Science.gov (United States)

    Naqvi, A A; Maslehuddin, M; ur-Rehman, Khateeb; Al-Amoudi, O S B

    2015-11-01

    The intensity of prompt gamma-ray was measured at various depths from chlorine-contaminated silica fume (SF) concrete slab concrete specimens using portable neutron generator-based prompt gamma-ray setup. The intensity of 6.11MeV chloride gamma-rays was measured from the chloride contaminated slab at distance of 15.25, 20.25, 25.25, 30.25 and 35.25cm from neutron target in a SF cement concrete slab specimens. Due to attenuation of thermal neutron flux and emitted gamma-ray intensity in SF cement concrete at various depths, the measured intensity of chlorine gamma-rays decreases non-linearly with increasing depth in concrete. A good agreement was noted between the experimental results and the results of Monte Carlo simulation. This study has provided useful experimental data for evaluating the chloride contamination in the SF concrete utilizing gamma-ray attenuation method.

  19. Kinetics of aqueous chlorination of some pharmaceuticals and their elimination from water matrices.

    Science.gov (United States)

    Acero, Juan L; Benitez, F Javier; Real, Francisco J; Roldan, Gloria

    2010-07-01

    Apparent rate constants for the reactions of four selected pharmaceutical compounds (metoprolol, naproxen, amoxicillin, and phenacetin) with chlorine in ultra-pure (UP) water were determined as a function of the pH. It was found that amoxicillin (in the whole pH range 3-12), and naproxen (in the low pH range 2-4) presented high reaction rates, while naproxen (in the pH range 5-9), and phenacetin and metoprolol (in the pH range 2.5-12 for phenacetin, and 3-10 for metoprolol) followed intermediate and slow reaction rates. A mechanism is proposed for the chlorination reaction, which allowed the evaluation of the intrinsic rate constants for the elementary reactions of the ionized and un-ionized species of each selected pharmaceutical with chlorine. An excellent agreement is obtained between experimental and calculated rate constants by this mechanism.The elimination of these substances in several waters (a groundwater, a surface water from a public reservoir, and two effluents from municipal wastewater treatment plants) was also investigated at neutral pH. The efficiency of the chlorination process with respect to the pharmaceuticals elimination and the formation THMs was also established. It is generally observed that the increasing presence of organic and inorganic matter in the water matrices demand more oxidant agent (chlorine), and therefore, less chlorine is available for the oxidation of these compounds. Finally, half-life times and oxidant exposures (CT) required for the removal of 99% of the four pharmaceuticals are also evaluated. These parameters are useful for the establishment of safety chlorine doses in oxidation or disinfection stages of pharmaceuticals in treatment plants.

  20. Corrosion of copper by chlorine trifluoride

    International Nuclear Information System (INIS)

    The research described called for a considerable amount of preliminary development of the test methods and equipment in order that the various measurements and observations could be carried out without contaminating either the samples or this highly reactive gas. The chlorine trifluoride was highly purified before use, its purity being checked by gas-phase chromatography, micro-sublimation and infrared spectrography. The tests were carried out on copper samples of various purities, in particular a 99.999 per cent copper in the form of mono-crystals. They involved kinetic measurements and the characterization of corrosion products under different temperature and pressure conditions. The kinetics showed reactions of the same order of magnitude as those obtained with elementary fluorine. At atmospheric pressure there occurs formation of cupric fluoride and cuprous chloride. The presence of this latter product shows that it is not possible to consider ClF3 simply as a fluorinating agent. At low pressures an unknown product has been characterized. There are strong grounds for believing that it is the unstable cuprous fluoride which it has not yet been possible to isolate. A germination phenomenon has been shown to exist indicating an analogy between the initial phases of fluorination and those of oxidation. Important effects resulting from the dissociation of the copper fluorides and the solubility of chlorine in this metal have been demonstrated. Finally, tests have shown the considerable influence of the purity of the gas phase and of the nature of the reaction vessel walls on the rates of corrosion which can in certain cases be increased by a factor of several powers of ten. (author)

  1. 二氧化氯/TiO2光催化氧化降解碱性品红模拟废水及反应机理%Investigation of Chlorine Dioxide/TiO2 Photocatalytic Oxidative Degradation of Simulated Wastewater Containing Fuchsine and Its Reaction Mechanism

    Institute of Scientific and Technical Information of China (English)

    施来顺; 王晓美

    2012-01-01

    The photocatalyst TiO2 was prepared by dipping-calcination method using silica gel as catalyst support.The chlorine dioxide/TiO2 photocatalyst was used for the photocatalytic oxidation of simulated fuchsine wastewater.The degradation effect of fuchsine by the combination of chlorine dioxide,TiO2 photocatalyst and UV irradiation was confirmed by comparison test.The optimum treatment conditions were as follows:the volume of wastewater containing 150 mg·L-1 fuchsine was 50 mL;ClO2 concentration was 6.14 mg·L-1,pH value was 5.0;the distance between UV lamp and flask was 20 cm;UV irradiation time was 13 min;and photocatalyst dosage was 10 g·L-1.The removal efficiency of fuchsine could reach 80%,compared with 46% of chlorine dioxide chemical oxidation.With UV-vis and FT IR analysis technique,the intermediates in the degradation process were obtained.Fuchsine was degradated into quinone and carboxylic acid,and finally changed into carbon dioxide and water during the photocatalytic oxidation.The degradation reaction mechanism of fuchsine by chlorine dioxide/TiO2 photocatalytic oxidation was proposed.%以硅胶为载体,采用浸渍-焙烧法制备了TiO2光催化剂,并将其用于二氧化氯/TiO2光催化氧化降解碱性品红模拟废水.经对比实验验证了ClO2/TiO2光催化剂/UV照射对碱性品红的氧化降解作用.50 mL质量浓度为150 mg.L-1的碱性品红模拟废水,在pH值为5.0,二氧化氯质量浓度6.14 mg.L-1和10 g.L-1光催化剂条件下,紫外照射距离20 cm,紫外照射时间13 min,碱性品红的去除率可达80%,远远高于二氧化氯化学氧化处理碱性品红的去除率46%.在废水处理过程中,采用紫外可见光谱和红外光谱分析降解产物,碱性品红被氧化降解为醌和羧酸,并进一步降解为二氧化碳和水,提出了二氧化氯/TiO2光催化氧化降解碱性品红废水的反应机理.

  2. The effect of chlorine and combined chlorine/UV treatment on coliphages in drinking water disinfection.

    Science.gov (United States)

    Zyara, Alyaa M; Torvinen, Eila; Veijalainen, Anna-Maria; Heinonen-Tanski, Helvi

    2016-08-01

    Chlorine disinfection is a globally used method to ensure the safety of drinking water. However, it has not always been successful against viruses and, therefore, it is important to find new methods to disinfect water. Seventeen different coliphages were isolated from the treated municipal wastewater. These coliphages and MS2 were treated with different dosages of chlorine in drinking water, and a combined chlorine/ultraviolet irradiation treatment for the chlorine-resistant coliphages. Chlorine disinfection with 0.3-0.5 mg/L total chlorine (free Cl-dosage 0.12-0.21 mg/L) for 10 min achieved 2.5-5.7 Log10-reductions for 11 sensitive coliphages. The six most resistant coliphages showed no reduction with these chlorine concentrations. MS2 was intermediate in chlorine resistance, and thus it is not a good indicator for viruses in chlorine disinfection. In the combined treatment total chlorine of 0.05-0.25 mg/L (free Cl-dosage 0.02-0.08 mg/L) and ultraviolet irradiation (14-22 mWs/cm(2)) were more effective than chlorine alone, and 3-5 Log10-reductions were achieved for the chlorine-resistant strains. The chlorination efficiency could be increased by higher dosages and longer contact times, but this could increase the formation of disinfection by-products. Therefore, the combination treatment is a recommended disinfection method.

  3. Sorption- and diffusion-associated isotope effects for chlorinated and non chlorinated aromatic hydrocarbons in a sediment pore water diffusion sampler

    Science.gov (United States)

    Passeport, E.; Chu, K.; Lacrampe Couloume, G.; Landis, R.; Lutz, E. J.; Mack, E. E.; West, K.; Sherwood Lollar, B.

    2013-12-01

    Compound Specific Isotope Analysis (CSIA) has gained prominence for evaluation of microbial and abiotic degradation processes governing the fate of organic contaminants in groundwater. At the sediment pore water interface, in wetland or river bottom sediments, variations in oxidation-reduction conditions can affect reaction mechanisms and hence the contaminant mass flux discharged to surface waters. Carbon isotope fractionation has been shown to be an important tool in identifying the effects of degradation and differentiating between different degradation pathways. To date, while passive diffusion samplers (commonly called 'peepers') have provided a powerful tool for high spatial resolution sampling for dissolved VOC across the sediment water interface, peepers' compatibility with CSIA has never been evaluated. The operating principle of peepers involves compound diffusion from the sediment pore water to the peeper chambers via a membrane. In this study, we evaluated the isotope effects of diffusion through, and possible adsorption to a polysulfone membrane for priority groundwater contaminants including chlorinated and non-chlorinated aromatic hydrocarbons. Chlorinated benzenes tend to accumulate in the food web and therefore represent a significant threat to water resources. This is due to their larger sorption coefficients (Koc) and higher hydrophobicity properties (logKow) compared to other commonly-studied compounds (e.g., chlorinated ethenes). Application of CSIA to BTEX and chlorinated ethenes has demonstrated that non-degradative processes (e.g., sorption, volatilization, diffusion) typically result in smaller carbon isotope fractionation compared to degradative processes that involve breaking bonds. The large sorption properties of chlorinated benzenes preclude a direct extrapolation to these compounds of existing data on sorption-associated isotope effects obtained on other compounds. To date, similar studies have not been done for chlorinated aromatics

  4. Catalytic hydrogen-chlorine exchange between chlorinated hydrocarbons under oxygen-free conditions

    NARCIS (Netherlands)

    van der Heijden, A.W.A.M.; Podkolzin, S.G.; Jones, M.E.; Bitter, J.H.; Weckhuysen, B.M.

    2008-01-01

    Chlorinated hydrocarbons (CHCs) remain important industrial chemical intermediates and solvents, especially for the exploration of the potential of La-based materials for the conversion of chlorinated waste compounds.[1] The production of industrially important CHCs frequently occurs with concurrent

  5. Fracturing graphene by chlorination: a theoretical viewpoint

    OpenAIRE

    Ijäs, M.; Havu, P.; Harju, A.

    2012-01-01

    Motivated by the recent photochlorination experiment [B. Li et al., ACS Nano 5, 5957 (2011)], we study theoretically the interaction of chlorine with graphene. In previous theoretical studies, covalent binding between chlorine and carbon atoms has been elusive upon adsorption to the graphene basal plane. Interestingly, in their recent experiment, Li et al. interpreted their data in terms of chemical bonding of chlorine on top of the graphene plane, associated with a change from sp2 to sp3 in ...

  6. EFFICIENCY PROBLEMS RELATED TO PERMANGANATE OXIDATION SCHEMES

    Science.gov (United States)

    Oxidation schemes for the in-situ destruction of chlorinated solvents, using potassium permanganate, are receiving considerable attention. Indication from field studies and from our own work are that permanganate oxidation schemes have inherent problems that could severely limit...

  7. Dry Machining Tool Design via Chlorine Ion Implantation

    Institute of Scientific and Technical Information of China (English)

    TatsuhikoAizawa; AtsushiMitsuo; ShigeoYamamoto; ShinjiMuraishi; TaroSumitomo

    2004-01-01

    Dry machining has become a key issue to significantly reduce the wastes of used lubricants and cleaning agents and to improve the environmental consciousness for medical and food applications of special tooling. Since the tools and metallic works are in direct contact in dry, severe adhesive wear and oxidation are thought to occur even at the presence of hard protective coatings. Self-lubrication mechanism with use of lubricous oxide films is found to be effective for dry machining. Through the chlorine ion implantation to tools, titanium base oxides are in-situ formed on the tool surface. This oxide deforms elasto-plastically so that both friction coefficient and wear volume are reduced even in the high-speed cutting.

  8. Dry Machining Tool Design via Chlorine Ion Implantation

    Institute of Scientific and Technical Information of China (English)

    Tatsuhiko Aizawa; Atsushi Mitsuo; Shigeo Yamamoto; Shinji Muraishi; Taro Sumitomo

    2004-01-01

    Dry machining has become a key issue to significantly reduce the wastes of used lubricants and cleaning agents and to improve the environmental consciousness for medical and food applications of special tooling. Since the tools and metallic works are in direct contact in dry, severe adhesive wear and oxidation are thought to occur even at the presence of hard protective coatings. Self-lubrication mechanism with use of lubricous oxide films is found to be effective for dry machining. Through the chlorine ion implantation to tools, titanium base oxides are in-situ formed on the tool surface.This oxide deforms elasto-plastically so that both friction coefficient and wear volume are reduced even in the high-speed cutting.

  9. Potassium chloride production by microcline chlorination

    Energy Technology Data Exchange (ETDEWEB)

    Orosco, Pablo, E-mail: porosco@unsl.edu.ar [Instituto de Investigaciones en Tecnología Química (INTEQUI), Chacabuco y Pedernera, San Luis (Argentina); Facultad de Química, Bioquímica y Farmacia, Universidad Nacional de San Luis, Chacabuco y Pedernera, San Luis (Argentina); Ruiz, María del Carmen [Instituto de Investigaciones en Tecnología Química (INTEQUI), Chacabuco y Pedernera, San Luis (Argentina)

    2015-08-10

    Highlights: • Use of chlorination for the KCl production. • The reagents used were microcline, hydromagnesite and chlorine. • Isothermal and non-isothermal assays were performed in Cl{sub 2}–N{sub 2} mixture. • The chlorination generated KCl at 700 °C. • The chlorination products promote KCl formation. - Abstract: The potassium chloride is one of the most important fertilizers used in agriculture. The current demand of this salt makes interesting the study of potassium chloride production from unconventional potassium resources. In this work the potassium chloride production by chlorination of microcline was investigated. The starting reagents were microcline, hydromagnesite and chlorine. Non-isothermal and isothermal chlorination assays were carried out in a thermogravimetric device adapted to work in corrosive atmospheres. The temperature effect on potassium extraction and the phase transformations produced during chlorination of microcline were studied. The reagents and reaction products were analyzed by X-ray fluorescence (XRF) and X-ray diffraction (XRD). The experimental results indicated that by chlorination of microcline an important extraction of potassium in the temperature range from 800 to 900 °C was produced. Moreover, at 800 °C the forsterite, enstatite and magnesium aluminate spinel phases were generated.

  10. The chlorination of cyclopentanone and cyclohexanone

    NARCIS (Netherlands)

    Maatman, Hendrik

    1980-01-01

    In this thesis the results of an investigation of the chlorination of cyclopentanone and cyclohexanone in the solvent carbontetrachloride and catalyzed by hydrogen chloride are described. ... Zie: Summary

  11. High resolution spectrophotometry for identification of chlorine dioxide in concentrated chlorine solutions.

    Science.gov (United States)

    Gauw, R D; Emmert, G L; Bubnis, B; Gordon, G

    1999-12-01

    Electrolyzed salt brine generators hold great promise for water disinfection in small communities and remote locations. Electrolysis cell liquors have been reported to contain chlorine, chlorine dioxide and ozone. High resolution spectrophotometry was used to observe the presence (or absence) of a unique spectral absorbance pattern present in solutions containing 1-2 mg/l chlorine dioxide. PMID:18967802

  12. Behavior of chlorine in lake water

    International Nuclear Information System (INIS)

    Water from monsoon fed Sagre lake is being used as a source of raw water for Tarapur Atomic Power Station (TAPS--1 and 2). The raw water from the lake is initially pumped to Sagre water treatment plant (SWTP) operated by Maharashtra Industrial Development Corporation (MIDC) from where, the processed water is sent to cater the needs of both the units of TAPS-1 and 2, townships of TAPS and MIDC, and the nearby villages. At the SWTP the raw water is treated with alum to remove the turbidity, filtered and chlorinated using bleaching powder. All these years the raw water is chlorinated in such a way whereby a residual chlorine level of 0.5-1.0 mg/l, is maintained at the outlet of water treatment plant. The adequacy of the current chlorination practice was investigated, at the request of the NPC-500 MWe group during 1990, so that the future requirements of raw water for TAPP-3 and 4, can be met from the expanded SWTP. In this connection experiments on chlorine dose -- residual chlorine relationship and the decay pattern of chlorine with time was carried out in the lake water (with low value of total dissolved solids and total hardness 3 sample at the site. The total bacterial count in the raw water observed to be 107 counts/ml originally came down to 103 counts/ml at the end of one-hour exposure time to chlorine. It was found that the chlorine demand of the water was around 6 mg/l. In addition Jar test to evaluate the aluminum dose was also carried out. Based on these experiments a chlorine dose of 6 mg/l for one hour contact time was arrived at. The experimental findings were in agreement with the current chlorination practices. (author)

  13. Dechlorination progress of chlorinated organic pollutants degraded by use of ionizing radiation in aqueous solutions

    International Nuclear Information System (INIS)

    Kinetics and mechanisms of dechlorination of chlorinated organic pollutants induced by ionizing radiation were described in this article. The progress on the dechlorination of chlorophenols, polychlorinated biphenyl, trichloroethylene, and perchloroethylene involved in radiolysis was also reviewed. In oxidative condition, hydroxyl radical (·OH) would attack chlorophenol to form ·OH-adducts, which could be dechlorinated gradually. However, chlorophenol can be directly reduced by hydrated electron (eaq-) to release Cl-. It was found that radiolytic degradation of polychlorinated biphenyls in organic solvent would release chlorine atoms gradually by chain reactions and the final products were Cl- and biphenyl. Trichloroethylene and tetrachloroethylene mainly reacted with ·OH with the final products of CO2, HCOOH and HCI. As conclusion, the reductive dechlorination of chlorinated organic pollutants possesses advantages of high degradation efficiency, simple products and relatively low radiation dose compared with the oxidation methods. (authors)

  14. Inactivation of simian rotavirus SA11 by chlorine, chlorine dioxide, and monochloramine.

    OpenAIRE

    Berman, D.; Hoff, J C

    1984-01-01

    The kinetics of inactivation of simian rotavirus SA11 by chlorine, chlorine dioxide, and monochloramine were studied at 5 degrees C with a purified preparation of single virions and a preparation of cell-associated virions. Inactivation of the virus preparations with chlorine and chlorine dioxide was studied at pH 6 and 10. The monochloramine studies were done at pH 8. With 0.5 mg of chlorine per liter at pH 6, more than 4 logs (99.99%) of the single virions were inactivated in less than 15 s...

  15. Biodegradation of chlorinated ethenes by a methane-utilizing mixed culture

    International Nuclear Information System (INIS)

    Chlorinated ethenes are toxic substances which are widely distributed groundwater contaminants and are persistent in the subsurface environment. Reports on the biodegradation of these compounds under anaerobic conditions which might occur naturally in groundwater show that these substances degrade very slowly, if at all. Previous attempts to degrade chlorinated ethenes aerobically have produced conflicting results. A mixed culture containing methane-utilizing bacteria was obtained by methane enrichment of a sediment sample. Biodegradation experiments carried out in sealed culture bottles with radioactively labeled trichloroethylene (TCE) showed that approximately half of the radioactive carbon had been converted to 14CO2 and bacterial biomass. In addition to TCE, vinyl chloride and vinylidene chloride could be degraded to products which are not volatile chlorinated substances and are therefore likely to be further degraded to CO2. Two other chlorinated ethenes, cis and trans-1,2-dichloroethylene, were shown to degrade to chlorinated products, which appeared to degrade further. A sixth chlorinated ethene, tetrachloroethylene, was not degraded by the methane-utilizing culture under these conditions. The biodegradation of TCE was inhibited by acetylene, a specific inhibitor of methane oxidation by methanotrophs. This observation supported the hypothesis that a methanotroph is responsible for the observed biodegradations

  16. Elimination of the reactivation process in the adhesion of chlorinated SBS rubber with polychloroprene adhesives

    Directory of Open Access Journals (Sweden)

    2007-04-01

    Full Text Available Chlorination treatment of a thermoplastic styrene-butadiene-styrene rubber (SBS with a 3 wt% solution of trichloroisocyanuric acid (TCI in methyl ethyl ketone (MEK introduces chlorinated and oxidized moieties on the rubber surface which increase its surface energy and produces surface microroughness. Consequently adhesion properties, evaluated by T-peel strength measurements in chlorinated SBS/solvent based-polyurethane adhesive/leather joints, are enhanced. In this study, two solvent-based polychloroprene adhesives (PCP0 and PCP30R have been considered as an alternative to the commonly used solvent-based polyurethane adhesive (PU. A thermoreactive phenolic resin was added to one of the polychloroprene adhesive formulations (PCP30R. This tackifier resin favors chlorination of the adhesive and reinforces the interface between the chlorinated adhesive and the chlorinated rubber surface. Besides, PCP30R adhesive does not need adhesive reactivation and considerable high T-peel strength value (5.7±0.3 kN/m was obtained. Elimination of the reactivation process implies a considerable improvement of the manufacturing process in the footwear industry.

  17. Transformation of benzophenone-type UV filters by chlorine: Kinetics, products identification and toxicity assessments.

    Science.gov (United States)

    Li, Jian; Ma, Li-yun; Xu, Li

    2016-07-01

    The present study focused on the kinetics, transformation pathways and toxicity of several benzophenone-type ultraviolet filters (BPs) during the water chlorination disinfection process. The transformation kinetics of the studied three BPs was found to be second-order reaction, which was dependent on the concentration of BPs and chlorine. The second-order rate constants increased from 86.7 to 975 M(-1) s(-1) for oxybenzone, 49.6-261.7 M(-1) s(-1) for 4-hydroxybenzophenone and 51.7-540 M(-1) s(-1) for 2-hydroxy-4-methoxybenzophenone-5-sulfonic acid with the increasing pH value from 6 to 8 of the chlorination disinfection condition. Then the transformation products (TPs) of these BPs were identified by HPLC-QTof analysis. Several transformation pathways, including electrophilic substitution, methoxyl substitution, ketone groups oxidation, hydrolysis, decarboxylation and ring cleavage reaction, were speculated to participate in the chlorination transformation process. Finally, according to the toxicity experiment on luminescent bacteria, Photobacterium phosphoreum, enhanced toxicity was observed for almost all the TPs of the studied BPs except for 2,2'-dihydroxy-4,4'-dimethoxybenzophenone; it suggested the formation of TPs with more toxic than the parent compounds during the chlorination process. The present study provided a foundation to understand the transformation of BPs during chlorination disinfection process, and was of great significance to the drinking water safety.

  18. Chlorination of oxybenzone: Kinetics, transformation, disinfection byproducts formation, and genotoxicity changes.

    Science.gov (United States)

    Zhang, Shujuan; Wang, Xiaomao; Yang, Hongwei; Xie, Yuefeng F

    2016-07-01

    UV filters are a kind of emerging contaminant, and their transformation behavior in water treatment processes has aroused great concern. In particular, toxic products might be produced during reaction with disinfectants during the disinfection process. As one of the most widely used UV filters, oxybenzone has received significant attention, because its transformation and toxicity changes during chlorine oxidation are a concern. In our study, the reaction between oxybenzone and chlorine followed pseudo-first-order and second-order kinetics. Three transformation products were detected by LC-MS/MS, and the stability of products followed the order of tri-chloro-methoxyphenoyl > di-chlorinated oxybenzone > mono-chlorinated oxybenzone. Disinfection byproducts (DBPs) including chloroform, trichloroacetic acid, dichloroacetic acid and chloral hydrate were quickly formed, and increased at a slower rate until their concentrations remained constant. The maximum DBP/oxybenzone molar yields for the four compounds were 12.02%, 6.28%, 0.90% and 0.23%, respectively. SOS/umu genotoxicity test indicated that genotoxicity was highly elevated after chlorination, and genotoxicity showed a significantly positive correlation with the response of tri-chloro-methoxyphenoyl. Our results indicated that more genotoxic transformation products were produced in spite of the elimination of oxybenzone, posing potential threats to drinking water safety. This study shed light on the formation of DBPs and toxicity changes during the chlorination process of oxybenzone.

  19. Investigation of Ohmic mechanism for chlorine-treated p-type GaN using x-ray photoelectron spectroscopy

    Science.gov (United States)

    Chen, Po-Sung; Lee, Ching-Ting

    2006-08-01

    To investigate the function and mechanism of oxidation, the surface of the chlorine-treated p-type GaN semiconductor was analyzed using x-ray photoelectron spectroscopy. The chlorinated surface treatment was performed by electrolyzing HCl chemical solution to generate HClO, which in turn could be used to oxidize the p-type GaN. The chlorinated surface treatment enhances the formation of GaOx on the GaN surface and removing GaOx layer from the surface thereafter leads to the creation of additional Ga vacancies. Consequently, more holes are generated as a result of the generated Ga vacancies. Therefore, a relatively higher Ohmic performance with a specific contact resistance of 6.1×10-6Ωcm2 can be obtained for Ni /Au metal contact subsequently patterned on the chlorine-treated p-type GaN via the enhanced formation of GaOx.

  20. Removal of iodide from water by chlorination and subsequent adsorption on powdered activated carbon.

    Science.gov (United States)

    Ikari, Mariya; Matsui, Yoshihiko; Suzuki, Yuta; Matsushita, Taku; Shirasaki, Nobutaka

    2015-01-01

    Chlorine oxidation followed by treatment with activated carbon was studied as a possible method for removing radioactive iodine from water. Chlorination time, chlorine dose, the presence of natural organic matter (NOM), the presence of bromide ion (Br⁻), and carbon particle size strongly affected iodine removal. Treatment with superfine powdered activated carbon (SPAC) after 10-min oxidation with chlorine (1 mg-Cl₂/L) removed 90% of the iodine in NOM-containing water (dissolved organic carbon concentration, 1.5 mg-C/L). Iodine removal in NOM-containing water increased with increasing chlorine dose up to 0.1 mg-Cl₂/L but decreased at chlorine doses of >1.0 mg-Cl₂/L. At a low chlorine dose, nonadsorbable iodide ion (I⁻) was oxidized to adsorbable hypoiodous acid (HOI). When the chlorine dose was increased, some of the HOI reacted with NOM to form adsorbable organic iodine (organic-I). Increasing the chlorine dose further did not enhance iodine removal, owing to the formation of nonadsorbable iodate ion (IO₃⁻). Co-existing Br⁻ depressed iodine removal, particularly in NOM-free water, because hypobromous acid (HOBr) formed and catalyzed the oxidation of HOI to IO₃⁻. However, the effect of Br⁻ was small in the NOM-containing water because organic-I formed instead of IO₃⁻. SPAC (median particle diameter, 0.62 μm) had a higher equilibrium adsorption capacity for organic-I than did conventional PAC (median diameter, 18.9 μm), but the capacities of PAC and SPAC for HOI were similar. The reason for the higher equilibrium adsorption capacity for organic-I was that organic-I was adsorbed principally on the exterior of the PAC particles and not inside the PAC particles, as indicated by direct visualization of the solid-phase iodine concentration profiles in PAC particles by field emission electron probe microanalysis. In contrast, HOI was adsorbed evenly throughout the entire PAC particle. PMID:25462731

  1. Kinetic model for predicting the concentrations of active halogens species in chlorinated saline cooling waters. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Haag, W.R.; Lietzke, M.H.

    1981-08-01

    A kinetic model has been developed for describing the speciation of chlorine-produced oxidants in seawater as a function of time. The model is applicable under a broad variety of conditions, including all pH range, salinities, temperatures, ammonia concentrations, organic amine concentrations, and chlorine doses likely to be encountered during power plant cooling water chlorination. However, the effects of sunlight are not considered. The model can also be applied to freshwater and recirculating water systems with cooling towers. The results of the model agree with expectation, however, complete verification is not feasible at the present because analytical methods for some of the predicted species are lacking.

  2. 21 CFR 173.300 - Chlorine dioxide.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Chlorine dioxide. 173.300 Section 173.300 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) SECONDARY DIRECT FOOD ADDITIVES PERMITTED IN FOOD FOR HUMAN CONSUMPTION Specific Usage Additives § 173.300 Chlorine...

  3. Elements from chlorine to calcium nuclear reactions

    CERN Document Server

    Kunz, Wunibald

    1968-01-01

    Nuclear Tables: Part II Nuclear Reactions, Volume 3: The Elements from Chlorine to Calcium contains tabulations of the nuclear reaction values of elements chlorine, argon, potassium, and calcium. These tabulations provide the calculated Q-values of the elements and their isotopes. This book will be of value to general chemistry researchers.

  4. Chlorine

    Science.gov (United States)

    ... Del.icio.us Digg Facebook Google Bookmarks Technorati Yahoo MyWeb Updates Subscribe Listen Page last reviewed April ... Del.icio.us Digg Facebook Google Bookmarks Technorati Yahoo MyWeb Download page Subscribe to RSS Get email ...

  5. Enhancing the efficacy of electrolytic chlorination for ballast water treatment by adding carbon dioxide.

    Science.gov (United States)

    Cha, Hyung-Gon; Seo, Min-Ho; Lee, Heon-Young; Lee, Ji-Hyun; Lee, Dong-Sup; Shin, Kyoungsoon; Choi, Keun-Hyung

    2015-06-15

    We examined the synergistic effects of CO2 injection on electro-chlorination in disinfection of plankton and bacteria in simulated ballast water. Chlorination was performed at dosages of 4 and 6ppm with and without CO2 injection on electro-chlorination. Testing was performed in both seawater and brackish water quality as defined by IMO G8 guidelines. CO2 injection notably decreased from the control the number of Artemia franciscana, a brine shrimp, surviving during a 5-day post-treatment incubation (1.8 and 2.3 log10 reduction in seawater and brackish water, respectively at 6ppm TRO+CO2) compared with water electro-chlorinated only (1.2 and 1.3 log10 reduction in seawater and brackish water, respectively at 6ppm TRO). The phytoplankton Tetraselmis suecica, was completely disinfected with no live cell found at >4ppm TRO with and without CO2 addition. The effects of CO2 addition on heterotrophic bacterial growth was not different from electro-chlorination only. Total residual oxidant concentration (TRO) more rapidly declined in electro-chlorination of both marine and brackish waters compared to chlorine+CO2 treated waters, with significantly higher amount of TRO being left in waters treated with the CO2 addition. Total concentration of trihalomethanes (THMs) and haloacetic acids (HAAs) measured at day 0 in brackish water test were found to be 2- to 3-fold higher in 6ppm TRO+CO2-treated water than in 6ppm TRO treated water. The addition of CO2 to electro-chlorination may improve the efficiency of this sterilizing treatment of ballast water, yet the increased production of some disinfection byproducts needs further study. PMID:25841887

  6. Enhancing the efficacy of electrolytic chlorination for ballast water treatment by adding carbon dioxide.

    Science.gov (United States)

    Cha, Hyung-Gon; Seo, Min-Ho; Lee, Heon-Young; Lee, Ji-Hyun; Lee, Dong-Sup; Shin, Kyoungsoon; Choi, Keun-Hyung

    2015-06-15

    We examined the synergistic effects of CO2 injection on electro-chlorination in disinfection of plankton and bacteria in simulated ballast water. Chlorination was performed at dosages of 4 and 6ppm with and without CO2 injection on electro-chlorination. Testing was performed in both seawater and brackish water quality as defined by IMO G8 guidelines. CO2 injection notably decreased from the control the number of Artemia franciscana, a brine shrimp, surviving during a 5-day post-treatment incubation (1.8 and 2.3 log10 reduction in seawater and brackish water, respectively at 6ppm TRO+CO2) compared with water electro-chlorinated only (1.2 and 1.3 log10 reduction in seawater and brackish water, respectively at 6ppm TRO). The phytoplankton Tetraselmis suecica, was completely disinfected with no live cell found at >4ppm TRO with and without CO2 addition. The effects of CO2 addition on heterotrophic bacterial growth was not different from electro-chlorination only. Total residual oxidant concentration (TRO) more rapidly declined in electro-chlorination of both marine and brackish waters compared to chlorine+CO2 treated waters, with significantly higher amount of TRO being left in waters treated with the CO2 addition. Total concentration of trihalomethanes (THMs) and haloacetic acids (HAAs) measured at day 0 in brackish water test were found to be 2- to 3-fold higher in 6ppm TRO+CO2-treated water than in 6ppm TRO treated water. The addition of CO2 to electro-chlorination may improve the efficiency of this sterilizing treatment of ballast water, yet the increased production of some disinfection byproducts needs further study.

  7. Formation of new brominated disinfection byproducts during chlorination of saline sewage effluents.

    Science.gov (United States)

    Ding, Guoyu; Zhang, Xiangru; Yang, Mengting; Pan, Yang

    2013-05-15

    Chlorination could be the most cost-effective method for disinfecting saline sewage effluents resulting from toilet flushing with seawater. Upon chlorination, the high levels of bromide ions in saline sewage effluents (up to 32 mg/L) can be oxidized to hypobromous acid/hypobromite, which could then react with organic matter in the sewage effluents to form brominated disinfection byproducts (Br-DBPs). In this study, primary and secondary saline sewage effluents were collected and chlorinated at different chlorine doses, and a powerful precursor ion scan method using ultra performance liquid chromatography/electrospray ionization-triple quadrupole mass spectrometry was adopted for detection and identification of polar Br-DBPs in these samples. With the new method, 54 major polar Br-DBPs were detected in the chlorinated saline effluents and six of them were newly identified as wastewater DBPs, including bromomaleic acid, 5-bromosalicylic acid, 3,5-dibromo-4-hydroxybenzaldehyde, 3,5-dibromo-4-hydroxybenzoic acid, 2,6-dibromo-4-nitrophenol, and 2,4,6-tribromophenol. The formation of polar Br-DBPs, especially those newly detected ones, during chlorination of the saline effluents was studied. For the secondary saline effluent, various polar Br-DBPs formed and reached their maximum levels at different chlorine doses, whereas for the primary saline effluent, the formation of polar Br-DBPs basically kept increasing with increasing chlorine dose. Compared with the secondary saline effluent, the primary saline effluent generated fewer and less Br-DBPs and rarely generated nitrogenous Br-DBPs.

  8. Ground State Reactions of nC60 with Free Chlorine in Water.

    Science.gov (United States)

    Wu, Jiewei; Benoit, Denise; Lee, Seung Soo; Li, Wenlu; Fortner, John D

    2016-01-19

    Facile, photoenhanced transformations of water-stable C60 aggregates (nC60) to oxidized, soluble fullerene derivatives, have been described as key processes in understanding the ultimate environmental fate of fullerene based materials. In contrast, fewer studies have evaluated the aqueous reactivity of nC60 during ground-state conditions (i.e., dark conditions). Herein, this study identifies and characterizes the physicochemical transformations of C60 (as nC60 suspensions) in the presence of free chlorine, a globally used chemical oxidant, in the absence of light under environmentally relevant conditions. Results show that nC60 undergoes significant oxidation in the presence of free chlorine and the oxidation reaction rates increase with free chlorine concentration while being inversely related to solution pH. Product characterization by FTIR, XPS, Raman Spectroscopy, TEM, XRD, TOC, collectively demonstrates that oxidized C60 derivatives are readily formed in the presence of free chlorine with extensive covalent oxygen and even chlorine additions, and behave as soft (or loose) clusters in solution. Aggregation kinetics, as a function of pH and ionic strength/type, show a significant increase in product stabilities for all cases evaluated, even at pH values approaching 1. As expected with increased (surface) oxidation, classic Kow partitioning studies indicate that product clusters are relatively more hydrophilic than parent (reactant) nC60. Taken together, this work highlights the importance of understanding nanomaterial reactivity and the identification of corresponding stable daughter products, which are likely to differ significantly from parent material properties and behaviors.

  9. Selective chlorination of natural organic matter: identification of previously unknown disinfection byproducts.

    Science.gov (United States)

    Lavonen, Elin E; Gonsior, Michael; Tranvik, Lars J; Schmitt-Kopplin, Philippe; Köhler, Stephan J

    2013-03-01

    Natural organic matter (NOM) serve as precursors for disinfection byproducts (DBPs) in drinking water production making NOM removal essential in predisinfection treatment processes. We identified molecular formulas of chlorinated DBPs after chlorination and chloramination in four Swedish surface water treatment plants (WTPs) using ultrahigh resolution Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR-MS). Chlorine-containing formulas were detected before and after disinfection and were therefore classified to identify DBPs. In total, 499 DBPs were detected, of which 230 have not been reported earlier. The byproducts had, as a group, significantly lower ratio of hydrogen to carbon (H/C) and significantly higher average carbon oxidation state (COS), double bond equivalents per carbon (DBE/C) and ratio of oxygen to carbon (O/C) compared to Cl-containing components present before disinfection and CHO formulas in samples taken both before and after disinfection. Electrophilic substitution, the proposed most significant reaction pathway for chlorination of NOM, results in carbon oxidation and decreased H/C while O/C and DBE/C is left unchanged. Because the identified DBPs had significantly higher DBE/C and O/C than the CHO formulas we concluded that chlorination of NOM during disinfection is selective toward components with relatively high double bond equivalency and number of oxygen atoms per carbon. Furthermore, choice of disinfectant, dose, and predisinfection treatment at the different WTPs resulted in distinct patterns in the occurrence of DBP formulas.

  10. The effect of chlorine dioxide on the formation of trihalomethanes; Dioxido de cloro y su efecto en la formacion de trihalometanos

    Energy Technology Data Exchange (ETDEWEB)

    Ciurana de Gay, C.

    2000-07-01

    The chlorine dioxide presents a high reactivity with certain organic and inorganic compounds. In the process of making water fit to drink, one of the most valued characteristics of the chlorine dioxide is the oxidation of the precursors of trihalomethanes, that allows their decrease in the drinking water. The generation of the chlorine dioxide is the oxidation of the precursors of trihalomethanes, that allows their decrease in the drinking water. The generation of the chlorine dioxide must be made at the dosage point. Both, the generation and its control can be made in an easy way. Since a few years ago, in the ETAP, in Montfulla, some researches are being carried out in order to decrease the concentration of trihalomethanes. In this work it is exposed the generation the dosage control and the reduction of trihalomethanes obtained through the dosage of the chlorine dioxide at different doses. (Author) 8 refs.

  11. Mass Transfer Study of Chlorine Dioxide Gas Through Polymeric Packaging Materials

    Science.gov (United States)

    A continuous system for measuring the mass transfer of gaseous chlorine dioxide (ClO2), a strong oxidizing agent and used in food and pharmaceutical packaging, through 10 different types of polymeric packaging material was developed utilizing electrochemical sensor as a detector. Permeability, diff...

  12. Two-phase ozonation of chlorinated organics

    International Nuclear Information System (INIS)

    In the last few years the amount of research being conducted in the field of single-phase ozonation has grown extensively. However, traditional aqueous-phase ozonation systems are limited by a lack of selective oxidation potential, low ozone solubility in water, and slow intermediate decomposition rates. Furthermore, ozone may decompose before it can be utilized for pollutant destruction since ozone can be highly unstable in aqueous solutions. Naturally occurring compounds such as NaHCO3 also affect ozone reactions by inhibiting the formation of OH-free radicals. To compensate for these factors, excess ozone is typically supplied to a reactor. Since ozone generation requires considerable electric power consumption (16 - 24 kWh/kg of O3), attempts to enhance the ozone utilization rate and stability should lead to more efficient application of this process to hazardous waste treatment. To improve the process, ozonation may be more efficiently carried out in a two-phase system consisting of an inert solvent (saturated with O3) contacted with an aqueous phase containing pollutants. The non-aqueous phase must meet the following criteria: (1) non-toxic, (2) very low vapor pressure, (3) high density (for ease of separation), (4) complete insolubility in water, (5) reusability, (6) selective pollutant extractability, (7) high oxidant solubility, and (8) extended O3 stability. Previously published studies (1) have indicated that a number of fluorinated hydrocarbon compounds fit these criteria. For this project, FC40 (a product of 3M Co.) was chosen due to its low vapor pressure (3 mm Hg) and high specific gravity (1.9). The primary advantages of the FC40 solvent are that it is non-toxic, reusable, has an ozone solubility 10 times that of water, and that 85 % of the ozone remains in the solvent even after 2 hours. This novel two-phase process has been utilized to study the rapid destruction of organic chlorine compounds and organic mixtures

  13. Occurrence of by-products of strong oxidants reacting with drinking water contaminants--scope of the problem.

    OpenAIRE

    Rice, R G; Gomez-Taylor, M

    1986-01-01

    This paper describes results of a detailed literature review of the organic and inorganic by-products that have been identified as being formed in aqueous solution with four of the strong oxidizing/disinfecting agents commonly employed in drinking water treatment. These agents are: chlorine, chlorine dioxide, chloramine, and ozone. Significant findings include the production of similar nonchlorinated organic oxidation products from chlorine, chlorine dioxide, and ozone. In addition, all three...

  14. THM reduction on water distribution network with chlorine dioxide as disinfectant

    International Nuclear Information System (INIS)

    A disinfectant change on water distribution network, by chlorine dioxide in that case, avoids THM formation. In the other hand it creates big doubts about utilization and analytical determination of another oxidant different to chlorine. Just a need to comply the current legislation points us to make a change as the one mentioned above and carried out in DWTP Rio Verde, being managed by Acosol, where the THM formation is been reduced to 80%, according to the new limit of 100μg/l, along the 200 km of the supply network. (Author) 13 refs.

  15. Use of chlorination, ozonization and GAC adsorption to eliminate triazine pesticides in water supplies

    International Nuclear Information System (INIS)

    This study is focused on the research made between Facsa and Universidad de Zaragoza (Spain) related to the oxidation techniques application by chlorination and ozonization, and their combination with granular activated carbon (GAC) adsorption of mineral origin, in order to control triazine pesticides in water supplies. Experiments are carried out is a pilot plant. Although the chlorination or ozonization can partially degrade pesticides under study (atrazine, simazine, terbutilazine and bromacil), their passing through an adsorption column with GAC mineral, achieves their total removal when their initial concentrations are about 500 ng/l. These concentrations are obtained by fortification of studied sample. (Author) 9 refs

  16. Some kinetics aspects of chlorine-solids reactions

    Directory of Open Access Journals (Sweden)

    Kanari, N.

    2010-02-01

    Full Text Available The present paper describes detailed kinetics investigations on some selected chlorine-solid reactions through thermogravimetric measurements. The solids studied in this article include chemical pure oxides and sulfides as well as their natural bearing materials. The chlorinating agents employed are gaseous mixtures of Cl2+N2 (chlorination, Cl2+O2 (oxychlorination, and Cl2+CO (carbochlorination. Results are presented as effects of various parameters on the reaction rate of these solids with these chlorinating agents. It was observed that the reactivity of these solids towards different chlorinating agents varied widely. Sulfides could be chlorinated at room temperature, while carbochlorination of chromium (III oxide was possible only above 500 °C. The variation of the chlorination rate of these complex materials with respect to gas velocity, composition and temperature enabled us to focus some light on the plausible reaction mechanisms and stoichiometries. The obtained results were used for selective removal of iron from chromite concentrates, extraction of valuable metals from sulfide materials, purification of MgO samples, etc.

    Este trabajo describe detalladas investigaciones cinéticas en algunas reacciones seleccionadas de cloro-sólido a través de medidas termogravimétricas. Los sólidos estudiados en este artículo incluyen óxidos químicos puros y sulfuros, así como sus materiales naturales de soporte. Los agentes de cloración empleados son mezclas de gases de Cl2+N2 (cloración, Cl2+O2 (oxicloración y Cl2+O2 (carbocloración. Los resultados se presentan como efecto de varios parámetros en el porcentaje de reacción de estos sólidos con los agentes de cloración. Se ha observado que la reactividad de estos sólidos a través de diferentes agentes de cloración varía ampliamente. Los sulfuros se pudieron

  17. A comparison of the virucidal properties of chlorine, chlorine dioxide, bromine chloride and iodine.

    OpenAIRE

    Taylor, G R; Butler, M

    1982-01-01

    Chlorine dioxide, bromine chloride and iodine were compared with chlorine as virucidal agents. Under optimal conditions all disinfectants were effective at low concentrations, but each disinfectant responded differently to acidity and alkalinity. Disinfection by chlorine was impaired by the presence of ammonia, but the other disinfectants retained much of their potency. Disinfection of poliovirus by iodine resulted in structural changes in the virions as seen by electron micrroscopy, but the ...

  18. Chlorination of organic material in different soil types

    OpenAIRE

    Gustavsson, Malin

    2009-01-01

    Research has shown that formation of chlorinated organic matter occurs naturally and that organic chlorine is as abundant as the chloride ion in organic soils. A large number of organisms are known to convert inorganic chloride (Clin) to organic chlorine (Clorg) (e.g. bacteria, lichen, fungi and algae) and some enzymes associated to these organisms are capable of chlorinating soil organic matter. The aim with the study was to compare organic matter chlorination rates in soils from several dif...

  19. Ozone depletion and chlorine loading potentials

    Science.gov (United States)

    Pyle, John A.; Wuebbles, Donald J.; Solomon, Susan; Zvenigorodsky, Sergei; Connell, Peter; Ko, Malcolm K. W.; Fisher, Donald A.; Stordal, Frode; Weisenstein, Debra

    1991-01-01

    The recognition of the roles of chlorine and bromine compounds in ozone depletion has led to the regulation or their source gases. Some source gases are expected to be more damaging to the ozone layer than others, so that scientific guidance regarding their relative impacts is needed for regulatory purposes. Parameters used for this purpose include the steady-state and time-dependent chlorine loading potential (CLP) and the ozone depletion potential (ODP). Chlorine loading potentials depend upon the estimated value and accuracy of atmospheric lifetimes and are subject to significant (approximately 20-50 percent) uncertainties for many gases. Ozone depletion potentials depend on the same factors, as well as the evaluation of the release of reactive chlorine and bromine from each source gas and corresponding ozone destruction within the stratosphere.

  20. Why does Kevlar decompose, while Nomex does not, when treated with aqueous chlorine solutions?

    Science.gov (United States)

    Akdag, Akin; Kocer, Hasan B; Worley, S D; Broughton, R M; Webb, T R; Bray, Travis H

    2007-05-24

    Kevlar and Nomex are high-performance polymers which have wide varieties of applications in daily life. Recently, they have been proposed to be biocidal materials when reacted with household bleach (sodium hypochlorite solution) because they contain amide moieties which can be chlorinated to generate biocidal N-halamine functional groups. Although Nomex can be chlorinated without any significant decomposition, Kevlar decomposes under the same chlorination conditions. In this study, two mimics for each of the polymers were synthesized to simulate the carboxylate and diaminophenylene components of the materials. It was found that the p-diaminophenylene component of the Kevlar mimic is oxidized to a quinone-type structure upon treatment with hypochlorous acid, which then decomposes. However, such a mechanism for the Nomex mimic is not possible. In this paper, based upon these observations, a plausible answer will be provided to the title question. PMID:17465537

  1. Why does Kevlar decompose, while Nomex does not, when treated with aqueous chlorine solutions?

    Science.gov (United States)

    Akdag, Akin; Kocer, Hasan B; Worley, S D; Broughton, R M; Webb, T R; Bray, Travis H

    2007-05-24

    Kevlar and Nomex are high-performance polymers which have wide varieties of applications in daily life. Recently, they have been proposed to be biocidal materials when reacted with household bleach (sodium hypochlorite solution) because they contain amide moieties which can be chlorinated to generate biocidal N-halamine functional groups. Although Nomex can be chlorinated without any significant decomposition, Kevlar decomposes under the same chlorination conditions. In this study, two mimics for each of the polymers were synthesized to simulate the carboxylate and diaminophenylene components of the materials. It was found that the p-diaminophenylene component of the Kevlar mimic is oxidized to a quinone-type structure upon treatment with hypochlorous acid, which then decomposes. However, such a mechanism for the Nomex mimic is not possible. In this paper, based upon these observations, a plausible answer will be provided to the title question.

  2. Formation pathways of brominated products from benzophenone-4 chlorination in the presence of bromide ions

    Institute of Scientific and Technical Information of China (English)

    Ming Xiao; Dongbin Wei; Liping Li; Qi Liu; Huimin Zhao; Yuguo Du

    2014-01-01

    The brominated products,formed in chlorination treatment of benzophenone-4 in the presence of bromide ions,were identified,and the formation pathways were proposed.Under disinfection conditions,benzophenone-4 would undertake electrophilic substitution generating mono-or di-halogenated products,which would be oxidized to esters and further hydrolyzed to phenol derivatives.The generated catechol intermediate would be transformed into furan-like heterocyclic product.The product species were pH-dependent,while benzophenone-4 ehmination was chlorine dose-dependent.When the chlorination treatment was performed on ambient water spiked with benzophenone-4 and bromide ions,most of brominated byproducts could be detected,and the acute toxicity significantly increased as well.

  3. Hydrochloric acid recycling from chlorinated hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Sowieja, D. [Sulzer Escher Wyss GmbH, Ravensburg (Germany); Schaub, M. [Sulzer Chemtech Ltd., Winterthur (Switzerland)

    1993-12-31

    Chlorinated hydrocarbons present a major ecological hazard since most of them are only poorly biodegradable. Incineration is an economical process for their destruction, however the usually recovered sodium or calcium chlorides do not present a value and their disposal may even be very costly. Recovery of hydrochloric acid may therefore present an economical solution, mainly were large quantities of highly chlorinated compounds can be processed (author) 6 refs., 4 figs., 1 tab.

  4. Experimental studies on oxidizing removal of Cyclops of zooplankton

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    The inactivation of Cyclops with currently available oxidants such as chlorine, chlorine dioxide,ozone and potassium permanganate was investigated and reported under various working conditions of different oxidant dosage, organic substance content and pH value. The removal efficiency of Cyclops by predosing chlorine dioxide in water treatment process was comprehensively compared with that of the conventional prechlorination process. The results showed that chlorine dioxide might be most effective to inactivate Cyclops than other oxidants and its effect was less influenced by external conditions. Cyclops could be effectively inactivated by chlorine dioxide preoxidation and be thoroughly removed from water by chlorine dioxide preoxidation cooperating with routine clarification process, i.e. flocculation, sedimentation and filtration.

  5. Aqueous chlorination of mefenamic acid: kinetics, transformation by-products and ecotoxicity assessment.

    Science.gov (United States)

    Adira Wan Khalit, Wan Nor; Tay, Kheng Soo

    2016-05-18

    Mefenamic acid (Mfe) is one of the most frequently detected nonsteroidal anti-inflammatory drugs in the environment. This study investigated the kinetics and the transformation by-products of Mfe during aqueous chlorination. The potential ecotoxicity of the transformation by-products was also evaluated. In the kinetic study, the second-order rate constant (kapp) for the reaction between Mfe and free available chlorine (FAC) was determined at 25 ± 0.1 °C. The result indicated that the degradation of Mfe by FAC is highly pH-dependent. When the pH was increased from 6 to 8, it was found that the kapp for the reaction between Mfe and FAC was decreased from 16.44 to 4.4 M(-1) s(-1). Characterization of the transformation by-products formed during the chlorination of Mfe was carried out using liquid chromatography-quadrupole time-of-flight accurate mass spectrometry. Four major transformation by-products were identified. These transformation by-products were mainly formed through hydroxylation, chlorination and oxidation reactions. Ecotoxicity assessment revealed that transformation by-products, particularly monohydroxylated Mfe which is more toxic than Mfe, can be formed during aqueous chlorination.

  6. Investigation of heavy metal partitioning influenced by flue gas moisture and chlorine content during waste incineration.

    Science.gov (United States)

    Li, Qinghai; Meng, Aihong; Jia, Jinyan; Zhang, Yanguo

    2010-01-01

    The impact of moisture on the partitioning of the heavy metals including Pb, Zn, Cu and Cd in municipal solid waste (MSW) was studied in a laboratory tubular furnace. A thermodynamic investigation using CHEMKIN software was performed to compare the experimental results. Simulated waste, representative of typical MSW with and without chlorine compounds, was burned at the background temperature of 700 and 950 degrees C, respectively. In the absence of chlorine, the moisture content has no evident effect on the volatility of Pb, Zn and Cu at either 700 or 950 degrees C, however, as flue gas moisture increasing the Cd distribution in the bottom ash increased at 700 degrees C and reduced at 950 degrees C, respectively. In the presence of chlorine, the flue gas moisture reduced the volatility of Pb, Zn and Cu due to the transformation of the more volatile metal chlorides into less volatile metal oxides, and the reduction became significant as chlorine content increase. For Cd, the chlorine promotes its volatility through the formation of more volatile CdCl2. As a result, the increased moisture content increases the Pb, Zn, Cu and Cd concentrations in the bottom ash, which limits the utilization of the bottom ash as a construction material. Therefore, in order to accumulate heavy metals into the fly ash, MSW should be dried before incineration. PMID:20608514

  7. Formation potentials of typical DBPs and changes of genotoxicity for chlorinated tertiary effluent pretreated by ozone

    Institute of Scientific and Technical Information of China (English)

    CAO Nan; MIAO Tingting; LI Kuixiao; ZHANG Yu; YANG Min

    2009-01-01

    The effects of ozonation on the formation potential of typical disinfection byproducts (DBPs) and the changes of genotoxicity during post chlorination of tertiary effluent from a sewage treatment plant were investigated. Ozonation enhanced the yields of all detected chlorine DBPs except CHCl3. At a chlorine dose of 5 mg/L, the three brominated THMs and five HAAs increased, while chloroform decreased with the increase of ozone dose from 0 to 10 mg/L (ozone dose in consumption base). At a chlorine dose of 10 mg/L, the two mixed bromochloro species THMs and two dominant HAAs (DCAA and TCAA) firstly increased and then decreased with the increase of ozone dose, with the turning point approximately occurring at an ozone dose of 5 mg/L. The genotoxicity detected using umu test, on the other hand, was removed from 7 μg 4-NQO/L to a negligible level by ozonation under an ozone dose of 5 mg/L. Chlorination could further remove the genotoxicity to some extent. It was found that SUVA (UV absorbance divided by DOC concentration) might be used as an indicative parameter for monitoring the removal of genotoxicity during the oxidation.

  8. Chlorine Abundances in Cool Stars

    CERN Document Server

    Maas, Z G; Hinkle, K

    2016-01-01

    Chlorine abundances are reported in 15 evolved giants and one M dwarf in the solar neighborhood. The Cl abundance was measured using the vibration-rotation 1-0 P8 line of H$^{35}$Cl at 3.69851 $\\mu$m. The high resolution L-band spectra were observed using the Phoenix infrared spectrometer on the Kitt Peak Mayall 4m telescope. The average [$^{35}$Cl/Fe] abundance in stars with --0.72$<$[Fe/H]$<$0.20 is [$^{35}$Cl/Fe]=(--0.10$\\pm$0.15) dex. The mean difference between the [$^{35}$Cl/Fe] ratios measured in our stars and chemical evolution model values is (0.16$\\pm$0.15) dex. The [$^{35}$Cl/Ca] ratio has an offset of $\\sim$0.35 dex above model predictions suggesting chemical evolution models are under producing Cl at the high metallicity range. Abundances of C, N, O, Si, and Ca were also measured in our spectral region and are consistent with F and G dwarfs. The Cl versus O abundances from our sample match Cl abundances measured in planetary nebula and \\ion{H}{2} regions. In one star where both H$^{35}$Cl a...

  9. Establishment of the roadmap for chlorination process development for zirconium recovery and recycle

    International Nuclear Information System (INIS)

    Process development studies are being conducted to recover, purify, and reuse the zirconium (about 98.5% by mass) in used nuclear fuel (UNF) zirconium alloy cladding. Feasibility studies began in FY 2010 using empty cladding hulls that were left after fuel dissolution or after oxidation to a finely divided oxide powder (voloxidation). In FY 2012, two industrial teams (AREVA and Shaw-Westinghouse) were contracted by the Department of Energy Office of Nuclear Energy (NE) to provide technical assistance to the project. In FY 2013, the NE Fuel Cycle Research and Development Program requested development of a technology development roadmap to guide future work. The first step in the roadmap development was to assess the starting point, that is, the current state of the technology and the end goal. Based on previous test results, future work is to be focused on first using chlorine as the chlorinating agent and secondly on the use of a process design that utilizes a chlorination reactor and dual ZrCl4 product salt condensers. The likely need for a secondary purification step was recognized. Completion of feasibility testing required an experiment on the chemical decladding flowsheet option. This was done during April 2013. The roadmap for process development will continue through process chemistry optimization studies, the chlorinated reactor design configuration, product salt condensers, and the off-gas trapping of tritium or other volatile fission products from the off-gas stream. (authors)

  10. Sporicidal/bactericidal textiles via the chlorination of silk.

    Science.gov (United States)

    Dickerson, Matthew B; Lyon, Wanda; Gruner, William E; Mirau, Peter A; Slocik, Joseph M; Naik, Rajesh R

    2012-03-01

    Bacterial spores, such as those of the Bacillus genus, are extremely resilient, being able to germinate into metabolically active cells after withstanding harsh environmental conditions or aggressive chemical treatments. The toughness of the bacterial spore in combination with the use of spores, such as those of Bacillus anthracis, as a biological warfare agent necessitates the development of new antimicrobial textiles. In this work, a route to the production of fabrics that kill bacterial spores and cells within minutes of exposure is described. Utilizing this facile process, unmodified silk cloth is reacted with a diluted bleach solution, rinsed with water, and dried. The chlorination of silk was explored under basic (pH 11) and slightly acidic (pH 5) conditions. Chloramine-silk textiles prepared in acidified bleach solutions were found to have superior breaking strength and higher oxidative Cl contents than those prepared under caustic conditions. Silk cloth chlorinated for ≥1 h at pH 5 was determined to induce >99.99996% reduction in the colony forming units of Escherichia coli, as well as Bacillus thuringiensis Al Hakam (B. anthracis simulant) spores and cells within 10 min of contact. The processing conditions presented for silk fabric in this study are highly expeditionary, allowing for the on-site production of protein-based antimicrobial materials from a variety of agriculturally produced feed-stocks.

  11. Investigation of molybdenum pentachloride interaction with chlorine

    International Nuclear Information System (INIS)

    In Raman spectra of molybdenum pentachloride solutions in liquid chlorine lines were recorded in case of 397, 312, 410, 217 and 180 cm-1 vibrations of ν1(A1'), ν2(A1'), ν5(E'), ν6(E') and ν8(E'') monomer (symmetry D3h) molecules of MoCl5. Interaction of molten molybdenum pentachloride with chlorine at increased (up to 6 MPa) pressures of Cl2 was studied. In Raman spectra of its vapour distillation in liquid chlorine alongside with MoCl5 lines appearance of new lines at 363 and 272 cm-1, similar in their frequency to the ones calculated for the vibrations ν1(A1g) and ν2(Eg) of MoCl6 molecules (symmetry Oh), was observed

  12. Inactivation of antibiotic resistance genes in municipal wastewater by chlorination, ultraviolet, and ozonation disinfection.

    Science.gov (United States)

    Zhuang, Yao; Ren, Hongqiang; Geng, Jinju; Zhang, Yingying; Zhang, Yan; Ding, Lili; Xu, Ke

    2015-05-01

    This study investigated the inactivation of two antibiotic resistance genes (ARGs)-sul1 and tetG, and the integrase gene of class 1 integrons-intI1 by chlorination, ultraviolet (UV), and ozonation disinfection. Inactivation of sul1, tetG, and intI1 underwent increased doses of three disinfectors, and chlorine disinfection achieved more inactivation of ARGs and intI1 genes (chlorine dose of 160 mg/L with contact time of 120 min for 2.98-3.24 log reductions of ARGs) than UV irradiation (UV dose of 12,477 mJ/cm(2) for 2.48-2.74 log reductions of ARGs) and ozonation disinfection (ozonation dose of 177.6 mg/L for 1.68-2.55 log reductions of ARGs). The 16S rDNA was more efficiently removed than ARGs by ozone disinfection. The relative abundance of selected genes (normalized to 16S rDNA) increased during ozonation and with low doses of UV and chlorine disinfection. Inactivation of sul1 and tetG showed strong positive correlations with the inactivation of intI1 genes (for sul1, R (2)  = 0.929 with p disinfection, ozonation disinfection, Fenton oxidation, and coagulation), chlorination is an alternative method to remove ARGs from wastewater effluents. At a chlorine dose of 40 mg/L with 60 min contact time, the selected genes inactivation efficiency could reach 1.65-2.28 log, and the cost was estimated at 0.041 yuan/m(3).

  13. Of cabbages and chlorine: cholera in Peru.

    Science.gov (United States)

    1992-07-01

    The low case fatality rates (1%) from the 1991 cholera epidemic in Peru was more a result of including diarrheas of a less virulent etiology than that of cholera. In fact, a study during the early phases of the cholera epidemic in Trujillo, Peru revealed that only 79% of suspected cholera cases were infected with vibrio cholera 01. Further other people contended that the government of Peru did not chlorinate many water supplies because studies by the US Environmental Protection Agency suggested that chlorine increases the cancer risk. It reacts with organic matter to make trihalomethanes. 1 study noted that this risk may explain as many as 700 cases of cancer/year in the US, yet cholera was responsible for nearly 40009 deaths in Latin America the 1st year. Besides in Trujillo, Peru the reason for not chlorinating the water supply was not due to a conscious decision to not do so on the part of the government, but because no funds had been made available to purchase chlorinators and chlorine. This is typical of many towns in developing countries. Further raw fish also played a role in transmitting cholera in Peru. Moreover the study in Trujillo indicated that water stored in containers in the home, and not the water supply, was the most important vehicle of transmission. Nevertheless chlorination of both the water supply and stored water would have prevented cholera transmission. In addition, cabbage irrigated with raw wastewater contributed to cholera transmission in Trujillo. But a concern arises if developing countries follow the advice of WHO of 1st treating wastewater in stabilization ponds. Aquatic blue green algae, other zooplankton, and phytoplankton from a microhabitat suitable for V. cholera. In fact, a study in Peru identified a seasonal pattern of the cholera epidemic with the seasonality of V. cholera non-01 from sewage lagoons in Lima. PMID:1351603

  14. Atmospheric reactivity of alcohols, thiols and fluoroalcohols with chlorine atoms

    Science.gov (United States)

    Garzon Ruiz, Andres

    Alcohols, thiols and fluoroalcohols are volatile organic compounds (VOCs) which are emitted to the atmosphere from both natural (vegetation, oceans, volcanoes, etc.) and anthropogenic sources (fuels, solvents, wastewater, incinerators, refrigerants, etc.). These pollutants can be eliminated from the troposphere by deposition on the terrestrial surface, direct photolysis or reaction with different tropospheric oxidants. Reactions of VOCs with tropospheric oxidants are involved in the well-known atmospheric phenomenon of photochemical smog or the production of tropospheric ozone. The oxidation of these VOCs in the troposphere is mainly initiated by reaction with OH radicals during the daytime and with NO radicals at night. However, in recent years, the oxidation by chlorine atoms (Cl) has gained great importance in the study of atmospheric reactions because they may exert some influence in the boundary layer, particularly in marine and coastal environments. In general, Cl atoms are much more reactive species than OH and NO; radicals and therefore low concentrations of Cl may compete with OH and NO3 in hydrocarbon oxidation processes. The main source of tropospheric Cl atoms is believed to be the photolysis of chlorine-containing molecules generated by heterogeneous reactions of sea salt aerosols. It has also been proposed that Cl atoms, produced in the photolysis of Cl2 emitted from industrial processes, may enhance hydrocarbon oxidation rates and ozone production in urban environments. In this work, a kinetic, theoretical and mechanistic study of the reaction of several alcohols, thiols, and fluoroalcohols with Cl atoms has been carried out. Pulsed laser photolysis-fluorescence resonance (PLP-RF) technique was used for the kinetic study as a function of temperature and pressure. An environmental chamber-Fourier transform infrared (FTIR) system was also employed in the kinetic studies. Tropospheric lifetimes of these pollutants were estimated using obtained kinetic

  15. Occupational exposure to chlorinated and petroleum solvents and mycosis fungoides

    DEFF Research Database (Denmark)

    Morales-Suárez-Varela, Maria M; Olsen, Jørn; Villeneuve, Sara;

    2013-01-01

    To evaluate the potential association between occupational exposure to chlorinated and petroleum solvents and mycosis fungoides (MF).......To evaluate the potential association between occupational exposure to chlorinated and petroleum solvents and mycosis fungoides (MF)....

  16. The effects of low level chlorination and chlorine dioxide on biofouling control in a once-through service water system

    International Nuclear Information System (INIS)

    Continuous chlorination has been successfully used for the control of Corbicula at a nuclear power plant located on the Chattahoochee River in southeastern Alabama, since 1986. The purpose of this study was to investigate further minimization of chlorine usage and determine if chlorine dioxide is a feasible alternative. Four continuous biocide treatments were evaluated for macro and microfouling control effectiveness, operational feasibility, and environmental acceptability. One semi-continuous chlorination treatment was also evaluated for macrofouling control effectiveness. Higher treatment residuals were possible with chlorine dioxide than with chlorination due to the river discharge limitations. At the levels tested, continuous chlorine dioxide was significantly more effective in providing both macro and microfouling control. Semi-continuous chlorination was just as effective as continuous chlorination for controlling macrofouling. The Corbicula treatment programs that were tested should all provide sufficient control for zebra mussels. Chlorine dioxide was not as cost effective as chlorination for providing macrofouling control. The semi-continuous treatment save 50% on chemical usage and will allow for the simultaneous treatment of two service water systems. Chlorite levels produced during the chlorine dioxide treatments were found to be environmentally acceptable. Levels of trihalomethanes in the chlorinated service water were less than the maximum levels allowed in drinking water

  17. Review of chlorination of zirconium dioxide

    International Nuclear Information System (INIS)

    A review of chlorination zirconium dioxide is presented.used semi batch process with vertical reactor, horizontal reactor and fluidized reactor. The feed were zircon dioxide from Aldrich, direct zircon sand and briquette of zircon sand. From the study it is obtained that the best reactor is vertical reactor.It needs modification of chlorination reactor and sublimator to obtain the larger conversion. It is come to reality that zirconium tetrachloride preparation by process is significant with zirconium tetrachloride from Aldrich. It needs the sequel research to get the best result of process. (author)

  18. Chlorinated organic compounds produced by Fusarium graminearum.

    Science.gov (United States)

    Ntushelo, Khayalethu

    2016-06-01

    Fusarium graminearum, a pathogen of wheat and maize, not only reduces grain yield and degrades quality but also produces mycotoxins in the infected grain. Focus has been on mycotoxins because of the human and animal health hazards associated with them. In addition to work done on mycotoxins, chemical profiling of F. graminearum to identify other compounds produced by this fungus remains critical. With chemical profiling of F. graminearum the entire chemistry of this fungus can be understood. The focus of this work was to identify chlorinated compounds produced by F. graminearum. Various chlorinated compounds were detected and their role in F. graminearum is yet to be understood. PMID:27165533

  19. Effects of the temperature and the irradiation on the behaviour of chlorine 37 in nuclear graphite: consequences on the mobility of chlorine 36 in irradiated graphites

    International Nuclear Information System (INIS)

    This thesis deals with the studies of the management of irradiated graphite wastes issued from the dismantling of the UNGG French reactors. This work focuses on the behavior of 36Cl. This radionuclide is mainly issued through the neutron activation of 35Cl by the reaction 35Cl(n, γ)36Cl, pristine chlorine being an impurity of nuclear graphite, present at the level of some at.ppm. 36Cl is a long lived radionuclide (about 300,000 years) and is highly soluble in water and mobile in concrete and clay. The solubilization of 36Cl is controlled by the water accessibility into irradiated graphite pores as well as by factors related to 36Cl itself such as its chemical speciation and its location within the irradiated graphite. Both speciation and chlorine location should strongly influence its behaviour and need to be taken into account for the choice of liable management options. However, data on radioactive chlorine features are difficult to assess in irradiated graphite and are mainly related to detection sensitivity problems. In this context, we simulated and evaluated the impact of the temperature, the irradiation and the radiolytic oxidation on the chlorine 36 behaviour. In order to simulate the presence of 36Cl, we implanted 37Cl into virgin nuclear graphite. Ion implantation has been widely used to study the lattice location, the diffusion and the release of fission and activation products in nuclear materials. Our results on the comparative effects of the temperature and the irradiation show that chlorine occurs in irradiated graphite on temperature and electronic and nuclear irradiation improve this effect. (author)

  20. Blends of caprolactam/caprolactone copolymers and chlorinated polymers

    NARCIS (Netherlands)

    Alberda van Ekenstein, G.O.R.; Deuring, H.; ten Brinke, G.; Ellis, T.S.

    1997-01-01

    The phase behaviour of blends of chlorinated polyethylene, polyvinyl chloride (PVC) and chlorinated PVC with random copolymers of caprolactone and caprolactam has been investigated and the results correlated with a binary interaction model. The known miscibility of polycaprolactone in the chlorinate

  1. Chlorine Gas: An Evolving Hazardous Material Threat and Unconventional Weapon

    Directory of Open Access Journals (Sweden)

    Jones, Robert MD

    2010-05-01

    Full Text Available Chlorine gas represents a hazardous material threat from industrial accidents and as a terrorist weapon. This review will summarize recent events involving chlorine disasters and its use by terrorists, discuss pre-hospital considerations and suggest strategies for the initial management for acute chlorine exposure events. [West J Emerg Med. 2010; 11(2:151-156.

  2. Surface reactivity of V2O5(001): Effects of vacancies, protonation, hydroxylation, and chlorination

    Science.gov (United States)

    Negreira, Ana Suarez; Aboud, Shela; Wilcox, Jennifer

    2011-01-01

    Using density-functional theory we analyze the thermodynamic stability of partially reduced, protonated, hydroxylated, and chlorinated V2O5(001) surfaces under flue gas conditions. These surfaces are characterized geometrically through surface relaxation calculations and electronically through charge distribution and density-of-states analysis to understand the change in surface reactivity under different pressure and temperature conditions, with a primary focus on coal-fired flue gas conditions. The stoichiometric surface is found to be the most favorable termination under flue gas conditions, but at low oxygen partial pressures (i.e., ultra-high-vacuum conditions) and elevated temperatures, the partially reduced V2O5(001) surfaces with one or two vanadyl oxygen vacancies are found to be stable. A surface semiconductor-to-metal transformation takes place with the addition of oxygen vacancies indicated by a decrease in the band gap. The protonation of the V2O5(001) surface only takes place at low oxygen partial pressures where the main source or sink of hydrogen atoms comes from H2. The study of the thermodynamic stability of protonated surfaces and surfaces with dissociated water with both H- and OH- groups indicated that these surfaces are not stable under flue gas conditions. Chlorinated surfaces were not stable under the flue gas and the coverage conditions tested. Larger HCl concentrations or smaller coverages may lead to stable chlorinated structures; however, the small coverages required to accurately represent the chlorine flue gas concentrations would require much larger unit-cell sizes that would be too computationally expensive. From this work it is evident that the stoichiometric surface of V2O5 is the most stable under flue gas conditions, and likely reactivity corresponding to NOx reduction, surface chlorination, and mercury oxidation stems from support effects on the vanadia catalyst, which influences the vanadium oxidation state and subsequent

  3. Mitigation of chlorine-induced lung injury by low-molecular-weight antioxidants

    OpenAIRE

    Leustik, Martin; Doran, Stephen; Bracher, Andreas; Williams, Shawn; Squadrito, Giuseppe L.; Schoeb, Trenton R.; Postlethwait, Edward; Matalon, Sadis

    2008-01-01

    Chlorine (Cl2) is a highly reactive oxidant gas used extensively in a number of industrial processes. Exposure to high concentrations of Cl2 results in acute lung injury that may either resolve spontaneously or progress to acute respiratory failure. Presently, the pathophysiological sequelae associated with Cl2-induced acute lung injury in conscious animals, as well as the cellular and biochemical mechanisms involved, have not been elucidated. We exposed conscious Sprague-Dawley rats to Cl2 g...

  4. INVESTIGATION OF INTERMITTENT CHLORINATION SYSTEM IN BIOLOGICAL EXCESS SLUDGE REDUCTION BY SEQUENCING BATCH REACTORS

    OpenAIRE

    A. Takdastan ، N. Mehrdadi ، A. A. Azimi ، A. Torabian ، G. Nabi Bidhendi

    2009-01-01

    The excessive biological sludge production is one of the disadvantages of aerobic wastewater treatment processes such as sequencing batch reactors. To solve the problem of excess sludge production, oxidizing some of the sludge by chlorine, thus reducing the biomass coefficient as well as the sewage sludge disposal may be a suitable idea. In this study, two sequencing batch reactors, each with 20 L volume and controlled by on-line system were used. After providing the steady state conditions i...

  5. Chlorinated organic compounds in urban river sediments

    Energy Technology Data Exchange (ETDEWEB)

    Soma, Y.; Shiraishi, H.; Inaba, K. [National Inst. of Environmental Studies, Tsukuba, Ibaraki (Japan)

    1995-12-31

    Among anthropogenic chemicals, many chlorinated organic compounds have been used as insecticides and detected frequently as contaminants in urban river sediments so far. However, the number and total amount of chemicals produced commercially and used are increasing year by year, though each amount of chemicals is not so high. New types of contaminants in the environment may be detected by the use of newly developed chemicals. Chlorinated organic compounds in the urban river sediments around Tokyo and Kyoto, large cities in Japan, were surveyed and recent trends of contaminants were studied. Contaminants of the river sediments in industrial areas had a variety, but PCB (polychlorinated biphenyls) was detected in common in industrial areas. Concentration of PCB related well to the number of factories on both sides of rivers, although the use of PCB was stopped 20 years ago. In domestic areas, Triclosan (5-chloro-2-(2,4-dichlorophenoxy)-phenol) and Triclocarban (3,4,4{prime}-trichlorocarbanilide)(both are contained in soap or shampoo for fungicides), p-dichlorobenzene (insecticides for wears) and TCEP(tris-chloroethyl phosphate) were detected. EOX(extracted organic halogen) in the sediments was 5 to 10 times of chlorinated organic compounds detected by GC/MS. Major part of organic halogen was suggested to be included in chlorinated organics formed by bleaching or sterilization.

  6. Chlorinated tyrosine derivatives in insect cuticle

    DEFF Research Database (Denmark)

    Andersen, Svend Olav

    2004-01-01

    , not-yet sclerotized cuticle of adult femur and tibia, the amounts increased rapidly during the first 24 h after ecdysis and more slowly during the next two weeks. Control analyses using stable isotope dilution mass spectrometry have confirmed that the chlorinated tyrosines are not artifacts formed...

  7. Cellular Response of the Amoeba Acanthamoeba castellanii to Chlorine, Chlorine Dioxide, and Monochloramine Treatments ▿

    OpenAIRE

    Mogoa, Emerancienne; Bodet, Charles; Morel, Franck; Rodier, Marie-Hélène; Legube, Bernard; Héchard, Yann

    2011-01-01

    Acanthamoeba castellanii is a free-living amoebae commonly found in water systems. Free-living amoebae might be pathogenic but are also known to bear phagocytosis-resistant bacteria, protecting these bacteria from water treatments. The mode of action of these treatments is poorly understood, particularly on amoebae. It is important to examine the action of these treatments on amoebae in order to improve them. The cellular response to chlorine, chlorine dioxide, and monochloramine was tested o...

  8. Anaerobic biodegradability and toxicity of wastewaters from chlorine and total chlorine-free bleaching of eucalyptus kraft pulps.

    NARCIS (Netherlands)

    Vidal, G.; Soto, M.; Field, J.; Mendez-Pampin, R.; Lema, J.M.

    1997-01-01

    Chlorine bleaching effluents are problematic for anaerobic wastewater treatment due to their high methanogenic toxicity and low biodegradability. Presently, alternative bleaching processes are being introduced, such as elemental chlorine-free (ECF) and total chlorine-free (TCF) bleaching. The methan

  9. Photo-assisted electrochemical degradation of simulated textile effluent coupled with simultaneous chlorine photolysis.

    Science.gov (United States)

    de Mello Florêncio, Thaíla; de Araújo, Karla Santos; Antonelli, Raissa; de Toledo Fornazari, Ana Luiza; da Cunha, Paula Cordeiro Rodrigues; da Silva Bontempo, Letícia Helena; de Jesus Motheo, Artur; Granato, Ana Claudia; Malpass, Geoffroy Roger Pointer

    2016-10-01

    The influence of chloride ion concentration during the photo-assisted electrochemical degradation of simulated textile effluent, using a commercial Ti/Ru0.3Ti0.7O2 anode, was evaluated. Initially, the effect of applied current and supporting electrolyte concentration on the conversion of chloride ions to form reactive chlorine species in 90 min of experiment was analyzed in order to determine the maximum production of reactive chlorine species. The optimum conditions encountered (1.5 A and 0.3 mol dm(-3) NaCl) were subsequently employed for the degradation of simulated textile effluent. The efficiency of the process was determined through the analysis of chemical oxygen demand (COD), total organic carbon (TOC), of the presence of organochlorine products and phytotoxicity. Photo-assisted electrochemical degradation was more efficient for COD and TOC removal than the electrochemical technique alone. With simultaneous UV irradiation, a reduced quantity of reactive chlorine was produced, indicating that photolysis of the chlorine species led to the formation of hydroxyl radicals. This fact turns a simple electrochemical process into an advanced oxidation process.

  10. Simultaneous Recovery of Hydrogen and Chlorine from Industrial Waste Dilute Hydrochloric Acid

    Directory of Open Access Journals (Sweden)

    N. Paidimarri

    2016-01-01

    Full Text Available Recovery of chlorine from byproduct HCl has inevitable commercial importance in industries lately because of insufficient purity or too low concentration to recycle it. Instead it is being neutralized in industries before disposing to meet stringent environmental conditions. Although recovery through catalytic oxidation processes is studied since the 19th century, their high operating conditions combined with sluggish reaction kinetics and low single pass conversions make electrolysis a better alternative. The present motive of this work is to develop a novel electrolysis process which in contrast to traditional processes effectively recovers both hydrogen and chlorine from dilute HCl. For this, an electrolytic cell with an Anionic Exchange Membrane has been designed which only allows the passage of chlorine anions from catholyte to anolyte separating the gasses in a single step. The catholyte can be as low as 3.59 wt% because of fixed anolyte concentration of 1.99 wt% which minimizes oxygen formation. Preliminary results show that the simultaneous recovery of hydrogen and chlorine is possible with high conversion up to 98%. The maximum current density value for 4.96 cm2 membrane surface area (70% active surface area is 2.54 kAm−2, which is comparable with reported commercial processes. This study is expected to be useful for process intensification of the same in a continuous process environment.

  11. Effects of electrode settings on chlorine generation efficiency of electrolyzing seawater

    Directory of Open Access Journals (Sweden)

    Guoo-Shyng Wang Hsu

    2015-12-01

    Full Text Available Electrolyzed water has significant disinfection effects, can comply with food safety regulations, and is environmental friendly. We investigated the effects of immersion depth of electrodes, stirring, electrode size, and electrode gap on the properties and chlorine generation efficiency of electrolyzing seawater and its storage stability. Results indicated that temperature and oxidation-reduction potential (ORP of the seawater increased gradually, whereas electrical conductivity decreased steadily in electrolysis. During the electrolysis process, pH values and electric currents also decreased slightly within small ranges. Additional stirring or immersing the electrodes deep under the seawater significantly increased current density without affecting its electric efficiency and current efficiency. Decreasing electrode size or increasing electrode gap decreased chlorine production and electric current of the process without affecting its electric efficiency and current efficiency. Less than 35% of chlorine in the electrolyzed seawater was lost in a 3-week storage period. The decrement trend leveled off after the 1st week of storage. The electrolyzing system is a convenient and economical method for producing high-chlorine seawater, which will have high potential applications in agriculture, aquaculture, or food processing.

  12. Degradation of microcystin-RR in water by chlorine dioxide

    Institute of Scientific and Technical Information of China (English)

    JI Ying; HUANG Jun-li; FU Jiao; WU Ming-song; CUI Chong-wei

    2008-01-01

    Due to the potent hepatotoxicity and tumor-promoting activity of microcystins, a successful removal of these toxins during drinking water treatment processes is of increasing concern. The oxidation kinetics of MC-RR by chlorine dioxide (C1O2)was studied with HPLC and characterization of the reacdon products was performed with UV-spectrometry, TOC and LC-MS. Our experimental results show that the oxidation process is a second order overall and a first order with respect to C1O2 and MC-RR.The activation energy of MC-RR degradation by C1O2 is 53.07 kJ/mol. The rate constant k of the action can be increased by increasing temperature and decreasing pH value and ranged from 6. 11x102 L/(mol.min) to 5.29x 102 L/(mol-min) at pH from 3.44 to 10.41 at 10 ℃. Reaction products were determined to be organic and volatile, because they could be almost removed from aqueous solution by heating for 15 min at 60 ℃. In addition, the main oxidation products have m/z values of 1072 and are identified as dihydroxy isomers of MC-RR.

  13. Toxic effects of chlorinated cake flour in rats.

    Science.gov (United States)

    Cunningham, H M; Lawrence, G A; Tryphonas, L

    1977-05-01

    Four experiments were conducted using weanling Wistar rats to determine whether chlorinated cake flour or its constituents were toxic. Levels of 0.2 and 1.0% chlorine added to unbleached cake flour significantly (p less than 0.01) reduced growth rate by 20.7 and 85.2% and increased liver weight relative to body weight by 16.7 and 25.3%, respectively. Lipids extracted from flour chlorinated at the same levels had similar effects. Rat chow diets containing 0.2 and 0.6% chlorine in the form of chlorinated wheat gluten reduced growth rate and increased liver weight as a percentage of body weight. A rat chow diet containing 0.2% chlorine as chlorinated flour lipids increased absolute liver weight by 40%, kidney by 20%, and heart by 10% compared to pair-fed controls. PMID:864787

  14. Relation between chlorine with the quality of crude water

    International Nuclear Information System (INIS)

    Chlorine as disinfection agent in drinking water was used widely since it was successfully been practiced in drinking water in Jersey City, 1908. Mostly, water treatment plants in Malaysia were using chlorine as disinfection agent to kill pathogen and contaminated materials that can be dangerous to consumer. Because of chlorine was a strongly disinfection agent, it also can react with another chemical components such as manganese, hydrogen, sulfides, ammonia and phenol in water. These reactions happen very fast, and chlorine will not react as disinfection agent unless all the organic and inorganic substitution presented in water reacts with chlorine. These reactions between components will increase demand of chlorine in water. The demand of chlorine in water must be filled before the free radical chlorine occurred. These free radical chlorine will decay into hypochlorous acid and hypochlorite ion that so important in disinfection process to kill pathogens and pollutants in water. Most of water treatment plant to maintain free chlorine up to 0.2 mg/ L in distribution system to consumer. These researches involved determination of parameters that can be trusted to react with the chlorine in nine sampling station along Semenyih River and four stations in water treatment plants. These parameters were determined from ammonia, cyanides, sulfides, phenol, phosphorus, nitrite, manganese, iron and sum of organic carbons. Overall, these researches concluded that ammonia and sum of organic carbons were the most compounds that react with the chlorine to produce tryhalometane and chloramines. Besides that, the concentration of cyanides compounds, sulfide, phenol, phosphorus, nitrite, manganese and iron also decrease after the chlorination process. Results can used to evaluate demanding levels of chlorine in Semenyih River. (author)

  15. Antiradiation effectiveness of the chlorine C

    International Nuclear Information System (INIS)

    At present ever more attention of the experimenters in the field of search of high-effective antiray means - is directed to development of preparations from bio-active substances of a natural origin. In this connection all greater interest is caused by researches of antiray activity of these compounds, distinguished, as a rule, from known preparations of synthetic manufacture of low toxicity, absence of expressed collateral effects and possibility of course application. It has biological (antiray) activity in dozes 5-10 mg/kg and chlorine C which is derivative of chlorophil A. At present it passes tests in oncology. Porphyrines (synthetic and natural) are recently subjected to wide study as potential medicinal means, due to their ability to be accumulated in bodies of the reticulo-endothelial system and proliferous tissues, as well as their physical-chemical characteristics (fluorescence, photosensitizing action, colouring). All this testifies for the benefit of perspective use of porphyrin for treatment and diagnostics of tumors. According to the above described properties of porphyrines there is that fact, that for some of them radioprotective properties are revealed during the injections as well as before and after radiation treatment. The above said has formed the basis for study of antiray properties of the chlorine C during the experiments on small-sized laboratory animals. Antiradiation effectivity of chlorine C was studied on the mice (CBA x C57 B1) F1. Chlorine C was applied in a wide range of dozes with its' use in 3 variants: before radiation treatment, after radiation treatment, combined (before and after radiation treatment). Radioprotective activity of chlorine C reduces at an increase of a time of the injection before radiation treatment and at other ways of injection (intramuscularly, subcutaneously, per os). Studies of medical activity of chlorine C in experiments on mice have shown, that the compound does not possess medical activity. The death of

  16. Comparative efficacy of chlorine and chlorine dioxide regimes for condenser slime control in seawater cooled heat exchangers

    Energy Technology Data Exchange (ETDEWEB)

    Murthy, P.S.; Veeramani, P.; Ershath, M.; Rajamohan, R.; Harinath, Y.V.; Mohan, T.V.K.; Venugopalan, V.P. [BARC Facilities, Water and Steam Chemistry Div., Kalpakkam, Tamil nadu (India)

    2010-07-01

    Chlorination has long been used as an effective and economic biocide for biofouling control in seawater cooling systems. However, the efficacy of chlorine is reduced in the presence of organic content of seawater and the inability of chlorine to effectively penetrate biofilms. Chlorine dioxide is being projected as a possible alternative to chlorine. Experiments were carried out with the help of a seawater circulating facility, in which direct comparison of the efficacy of the two biocides was possible using test condenser tube assemblies. The test condenser tubes made of titanium, SS 316L and Cu-Ni 90/10 were dosed with chlorine and chlorine dioxide. Each dose was evaluated for 30 days. Continuous and intermittent additions of chlorine (0.38 - 0.45 mg L{sup -1} TRO) and chlorine dioxide (0.4 - 0.5 mg L{sup -1}) were used, along with control. The flow velocity in the tubes was maintained at 1.5 m/s. Results of the study showed that the efficacy of the biocide to control biofilms depended on the biocide and the material. Continuous chlorination resulted in 75% reduction of viable counts on titanium, followed by 24% reduction on CuNi and 6% reduction on SS 316L surfaces, as compared to the control. When compared to continuous chlorination, increase in bacterial density in the tubes was observed at different regimes of intermittent chlorination. On SS 316L and Cu-Ni surfaces, intermittent chlorination for 1h, once every 3 h, appeared to give adequate protection. Continuous addition of chlorine dioxide resulted in 99% reduction of viable counts on titanium surfaces, followed by 28% reduction on SS 316 L surfaces and 52% reduction on Cu-Ni surfaces, as compared to the controls. The data indicate that the efficacy of biocides to control biofilms depend on not only the biocide and its frequency of application but also the material of construction. (author)

  17. Comparative efficacy of chlorine and chlorine dioxide regimes for condenser slime control in seawater cooled heat exchangers

    International Nuclear Information System (INIS)

    Chlorination has long been used as an effective and economic biocide for biofouling control in seawater cooling systems. However, the efficacy of chlorine is reduced in the presence of organic content of seawater and the inability of chlorine to effectively penetrate biofilms. Chlorine dioxide is being projected as a possible alternative to chlorine. Experiments were carried out with the help of a seawater circulating facility, in which direct comparison of the efficacy of the two biocides was possible using test condenser tube assemblies. The test condenser tubes made of titanium, SS 316L and Cu-Ni 90/10 were dosed with chlorine and chlorine dioxide. Each dose was evaluated for 30 days. Continuous and intermittent additions of chlorine (0.38 - 0.45 mg L-1 TRO) and chlorine dioxide (0.4 - 0.5 mg L-1) were used, along with control. The flow velocity in the tubes was maintained at 1.5 m/s. Results of the study showed that the efficacy of the biocide to control biofilms depended on the biocide and the material. Continuous chlorination resulted in 75% reduction of viable counts on titanium, followed by 24% reduction on CuNi and 6% reduction on SS 316L surfaces, as compared to the control. When compared to continuous chlorination, increase in bacterial density in the tubes was observed at different regimes of intermittent chlorination. On SS 316L and Cu-Ni surfaces, intermittent chlorination for 1h, once every 3 h, appeared to give adequate protection. Continuous addition of chlorine dioxide resulted in 99% reduction of viable counts on titanium surfaces, followed by 28% reduction on SS 316 L surfaces and 52% reduction on Cu-Ni surfaces, as compared to the controls. The data indicate that the efficacy of biocides to control biofilms depend on not only the biocide and its frequency of application but also the material of construction. (author)

  18. In Situ Bioremediation of Chlorinated Ethenes in Hydraulically-Tight Sediments: Challenges and Limitations

    Science.gov (United States)

    Zhang, M.; Yoshikawa, M.; Takeuchi, M.; Komai, T.

    2011-12-01

    Chlorinated ethenes, like perchloroethene (PCE) and trichloroethene (TCE), have been widely used by many industries, especially in developed countries like Japan. Because of their wide applications, lack of proper regulation, poor handing, storage and disposal practices in the past, chlorinated ethenes have become a type of the most prevalent contaminants for soils and groundwater pollution. For the sake of their degradability, bioremediation has been considered as a potentially cost-effective and environmentally friendly approach for cleanup of chlorinated ethenes in situ. In this presentation, we briefly overview the status of soil and groundwater pollution, the recent amendment of the Soil Contamination Countermeasures Act in Japan, comparison between the bioremediation and other techniques like pump and treat, and the mechanisms of reductive dechlorination, direct oxidation and co-metabolism of chlorinated ethenes. We then introduce and discuss some recent challenges and advancements in in-situ bioremediation including technologies for accelerating bio-degradation of chlorinated ethenes, technologies for assessing diffusive properties of dissolved hydrogen in hydraulically-tight soil samples, and combination of bioremediation with other techniques like electro-kinetic approach. Limiting factors that may cause incomplete remediation and/or ineffectiveness of bioremediation are examined from biochemical, geochemical and hydro-geological aspects. This study reconfirmed and illustrated that: 1) The key factor for an effective bioremediation is how to disperse a proper accelerating agent throughout the polluted strata, 2) The effective diffusion coefficient of dissolved hydrogen in geologic media is relatively big and is almost independent on their permeability, and 3) To effectively design and perform an accelerated bioremediation, a combination of natural migration with pressurized injection and/or other approaches, like electro-migration, for stimulating mass

  19. Examination of the potential of chlorine dioxide for use in zebra mussel veliger control

    Energy Technology Data Exchange (ETDEWEB)

    Rusznak, L.; Smolik, N.; Hale, L.; Freymark, S. [Ashland Chemical Company, Drew Division, Boonton, NJ (United States)

    1995-06-01

    Dreissena polymorpha (zebra mussel) veligers were treated with various concentrations of chlorine dioxide and exposed at several time intervals to determine the effectiveness of this oxidant as a veliger control agent. The direction of this testing was based on previous studies which determined the effectiveness of chlorine dioxide as a molluscicide for adult zebra mussel control. Zebra mussel veligers were collected from the Niagara River shoreline at an untreated site and tested using filtered river water from the same source. All testing was conducted on site at an industrial plant in order to insure the integrity of veligers collected for this study. The plankton wheel method was used to examine the effects of chlorine dioxide. This methodology involves intense microscopic examination of the test organism prior to and after chemical exposure todeterminen molluscicidal efficacy. Veliger mortality was determined based on observations of veliger movement. Typical criteria for the determination of mortality was expanded to include four categories; veliger actively swimming, internal musculature movement, no internal musculature movement observed, however not necessarily indicating a mortality and obviously a mortality. The treatment levels ranged from 0.75 ppm - 2.0 ppm which are considered to simulate treatment levels in actual applications. Mortality levels ranged on average from 16%-42% based on 30 minute or 60 minute exposure times. The determination exposure time was based on water flow time intervals in actural applications. Sodium hypochlorite was also evaluated in order to compare the effectiveness of chlorine dioxide against this known veliger control agent. Testing resulted in chlorine dioxide providing significantly better veliger control than sodium hypochlorite under similar conditions.

  20. Revisiting the thermochemistry of chlorine fluorides

    CERN Document Server

    Sánchez, H R

    2016-01-01

    In this work, accurate calculations of standard enthalpies of formation of chlorine fluorides (ClF$_n$, n=1--7; Cl$_2$F and Cl$_3$F$_2$) were performed through the isodesmic reactions scheme. It is argued that, for many chlorine fluorides, the gold standard method of quantum chemistry (CCSD(T)) is not capable to predict enthalpy values nearing chemical accuracy if atomization scheme is used. This is underpinned by a thorough analysis of total atomization energy results and the inspection of multireference features of these compounds. Other thermodynamic quantities were also calculated at different temperatures. In order to complement the energetic description, elimination curves were studied through density functional theory as a computationally affordable alternative to highly correlated wave function-based methods.

  1. Bacterial responses to reactive chlorine species.

    Science.gov (United States)

    Gray, Michael J; Wholey, Wei-Yun; Jakob, Ursula

    2013-01-01

    Hypochlorous acid (HOCl), the active ingredient of household bleach, is the most common disinfectant in medical, industrial, and domestic use and plays an important role in microbial killing in the innate immune system. Given the critical importance of the antimicrobial properties of chlorine to public health, it is surprising how little is known about the ways in which bacteria sense and respond to reactive chlorine species (RCS). Although the literature on bacterial responses to reactive oxygen species (ROS) is enormous, work addressing bacterial responses to RCS has begun only recently. Transcriptomic and proteomic studies now provide new insights into how bacteria mount defenses against this important class of antimicrobial compounds. In this review, we summarize the current knowledge, emphasizing the overlaps between RCS stress responses and other more well-characterized bacterial defense systems, and identify outstanding questions that represent productive avenues for future research. PMID:23768204

  2. Behavioral toxicology, risk assessment, and chlorinated hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Evangelista de Duffard, A.M.; Duffard, R. [Laboratorio de Toxicologia Experimental, Santa Fe (Argentina)

    1996-04-01

    Behavioral end points are being used with greater frequency in neurotoxicology to detect and characterize the adverse effects of chemicals on the nervous system. Behavioral measures are particularly important for neurotoxicity risk assessment since many known neurotoxicants do not result in neuropathology. The chlorinated hydrocarbon class consists of a wide variety of chemicals including polychlorinated biphenyls, clioquinol, trichloroethylene, hexachlorophene, organochlorine insecticides (DDT, dicofol, chlordecone, dieldrin, and lindane), and phenoxyherbicides. Each of these chemicals has effects on motor, sensory, or cognitive function that are detectable using functional measures such as behavior. Furthermore, there is evidence that if exposure occurs during critical periods of development, many of the chlorinated hydrocarbons are developmental neurotoxicants. Developmental neurotoxicity is frequently expressed as alterations in motor function or cognitive abilities or charges in the ontogeny of sensorimotor reflexes. Neurotoxicity risk assessment should include assessments of the full range of possible neurotoxicological effects, including both structural and functional indicators of neurotoxicity. 121 refs., 1 tab.

  3. Recent Achievements in the Radiation-Catalysed Chlorination of Chlorinated Pentane Derivatives

    International Nuclear Information System (INIS)

    The radiation-catalysed chlorination of the so-called tetrachloro-cyclopentane, the product obtained from cyclopentadiene by addition of chlorine, has already been studied earlier by the authors with success. On maintaining an adequate dosage rate, no ring cleavage occurs, and, mainly for stereochemical reasons, octachloro-cyclopentene forms as an end product - similarly to conventional chlorination carried out at high temperature (400-500oC), but at substantially lower temperature (170oC) and without any resin formation. It is known that besides other end products, octachloro-cyclopentene forms also from perchlorinated pentane, under simultaneous cyclization. In their recent experiments presented here, the authors investigated how and to what extent the yield of octachloro-cyclopentene is affected by additional chlorination of pentane, previously chlorinated under cooling (at 10 to 30oC). The experiments were carried out with a Co60 radiation source of 330 c at a dosage rate of 8 x 103 to 8 x 104r/hr, in a heated reaction mixture, mixed with a chlorine stream for periods not exceeding 30 hr. It was found that also this type of chlorination and cyclization takes place at a temperature substantially lower than the conventional 500-600oC. According to the experiments, in this case it is advisable to raise the initial temperature of 170oC of the reaction gradually to 220oC with the progress of the reaction, in order to promote the cyclization reaction. It was found, namely, that first the paraffin chain was further chlorinated and later the perchlorinated pentane derivatives cyclize partly to octachloro-cyclopentene, under formation of other chlorinated alkane and alkene derivatives. This reaction mechanism was also supported by thermodynamical calculations. The end product contains three main components; its content of octachloro-cyclopentene ranges between 25 and 35%. The data required for the evaluation of the economy of the method will be available only on the

  4. Fluoridation of gaseous phase chlorinated hydrocarbons in presence of chromium oxide-based catalysts. Effect of doping substance addition; Fluoration d'hydrocarbures chlores en phase gazeuse en presence de catalyseurs a base d'oxyde de chrome. Effet de l'ajout de dopant

    Energy Technology Data Exchange (ETDEWEB)

    Loustaunau, A.

    2003-11-01

    The preparation of various hydro-fluorocarbons (HFC), like CF{sub 3}CH{sub 2}F, CF{sub 3}CHF{sub 2} and CH{sub 2}F{sub 2}, has been studied at temperatures of 380 deg. C and 250 deg. C in gaseous phase by catalytic fluoridation of the corresponding chlorinated hydrocarbons. The addition of doping substances like zinc, nickel or magnesium to fluorinated alumina supported chromium oxide-based catalysts, has been particularly examined in order to favour the main fluoridation reaction (by simple Cl/F exchange) with respect to secondary reactions (de-hydro-fluoridation and Deacon). Only the addition of small amounts of Zn (Zn/(Zn+Cr) = 0.15) allows to promote the fluoridation reaction and to inhibit the secondary reactions. This effect is enhanced when the molecule is less reactive and when the quantity of matter at the surface of the fluorinated alumina is low. Therefore, the promoting effect is more important in presence of CF{sub 3}CH{sub 2}Cl than in presence of CF{sub 3}CHCl{sub 2} and CH{sub 2}Cl{sub 2}. This positive effect of zinc may result from the formation of a mixed ZnCr{sub 2}O{sub 4} phase during the preparation of the catalyst (evidenced by X-ray photoelectron spectroscopy (XPS)) which may have modified the chemical properties of chromium atoms. Moreover, the XPS and electron microscopy characterizations indicate that the presence of zinc (contrary to nickel and magnesium) may allow a better dispersion of the active chromium atoms for Cl/F exchanges after fluoridation of the catalyst. Those may correspond to the presence of very fluorinated species, like 'Cr-F', and oxi-fluorinated like 'CrOF'. Thus, in the presence of a small amount of metals at the surface of the support, the formation of these different species is favoured. (J.S.)

  5. Chlorine diffusion in CdTe

    Energy Technology Data Exchange (ETDEWEB)

    Sadaiyandi, K.; Ramachandran, K. (School of Physics, Madurai Kamaraj Univ. (India))

    1991-06-01

    The experimental results of chlorine diffusion in CdTe reveal that the dominant mechanism for diffusion is through neutral defect pair such as (V{sub Cd}V{sub Te}){sup *}. Here, theoretical calculations are carried out for all the possible mechanisms such as single vacancy, single interstitial, neutral defect pair, and Frenkel defect pair. The results suggest that the most possible mechanism for Cl diffusion in CdTe is that through neutral defect pair, supporting the experiment. (orig.).

  6. On normalization of chlorine content in the nitrogen dioxide based coolant

    International Nuclear Information System (INIS)

    From the viewpoint of thermodynamics ways to transform chlorine-containing impurities in nitrogen dioxide into nitrosyl chloride are analyzed. The effect of the impurities on coolant corrosion activity in case of their content up to 0.07 % in terms of chlorine is studied experimentally. The conclusion is made on the admissible content of chlorine compounds in nitrogen dioxide within 0.01-0.03 %. When the admissible content of chloride in the coolant subjected to high-temperature treatment is exceeded, the rectification purification is possible. Lines of phase equilibria in systems nitrogen dioxide-nitrosyl chloride and nitrogen dioxide-nitrogen oxide in the range of low concentration of highly volatile component practically coincide in liquid content-vapor content coordinates. A twofold decrease in nitrosyl chloride concentration in still bottoms is accompanied by the twofold decrease in nitrogen oxide concentration. For twofold decrease in nitrosyl chloride concentration in the process of degassing during boiling the evaporation of 30 % of coolant is required

  7. Radiolytic degradation of chlorinated hydrocarbons in water

    International Nuclear Information System (INIS)

    Radiolytic degradation of chlorinated hydrocarbons (chloroform, trichloroethylene, and tetrachloroethylene) in water was carried out. Water solutions of the chlorinated hydrocarbons with different concentrations were irradiated with γ rays. Concentrations of methane, ethane, CO, CO2, H2, and O2 after the irradiation were determined by gas chromatography. Concentration of chloride ion in the irradiated sample was determined by ion chromatography. Experimental results show that radiolytic degradation of the chlorinated hydrocarbon increased with the radiation dose. Methane, ethane, CO2, H2, and Cl- concentrations increased with the radiation dose and the sample concentration. On the other hand, O2 concentration decreased with the radiation dose and the sample concentration. When sample concentration was high, dissolved oxygen might be not enough for converting most of the C atoms in the sample into CO2. This resulted in a low decomposition ratio. Addition of H2O2 as an oxygen resource could increase the decomposition ratio greatly. Furthermore, gas chromatography-mass spectroscopy was applied to identify some intermediates of the radiolytic dehalogenation. Radiolytic degradation mechanisms are also discussed. (author)

  8. Formation potentials of typical disinfection byproducts and changes of genotoxicity for chlorinated tertiary effluent pretreated by ozone.

    Science.gov (United States)

    Cao, Nan; Miao, Tingting; Li, Kuixiao; Zhang, Yu; Yang, Min

    2009-01-01

    The effects of ozonation on the formation potential of typical disinfection byproducts (DBPs) and the changes of genotoxicity during post chlorination of tertiary effluent from a sewage treatment plant were investigated. Ozonation enhanced the yields of all detected chlorine DBPs except CHCl3. At a chlorine dose of 5 mg/L, the three brominated THMs and five HAAs increased, while chloroform decreased with the increase of ozone dose from 0 to 10 mg/L (ozone dose in consumption base). At a chlorine dose of 10 mg/L, the two mixed bromochloro species THMs and two dominant HAAs (DCAA and TCAA) increased firstly and then decreased with the increase of ozone dose, with the turning point approximately occurring at an ozone dose of 5 mg/L. The genotoxicity detected using umu test, on the other hand, was removed from 7 microg 4-NQO/L to a negligible level by ozonation under an ozone dose of 5 mg/L. Chlorination could further remove the genotoxicity to some extent. It was found that SUVA (UV absorbance divided by DOC concentration) might be used as an indicative parameter for monitoring the removal of genotoxicity during the oxidation.

  9. Enhanced Elemental Mercury Removal from Coal-fired Flue Gas by Sulfur-chlorine Compounds

    Energy Technology Data Exchange (ETDEWEB)

    Chang, Shih-Ger; Yan, Nai-Qiang; Qu, Zan; Chi, Yao; Qiao, Shao-Hua; Dod, Ray; Chang, Shih-Ger; Miller, Charles

    2008-07-02

    Oxidation of Hg0 with any oxidant or converting it to a particle-bound form can facilitate its removal. Two sulfur-chlorine compounds, sulfur dichloride (SCl2) and sulfur monochloride (S2Cl2), were investigated as oxidants for Hg0 by gas phase reaction and by surface-involved reactions in the presence of flyash or activated carbon. The gas phase reaction rate constants between Hg0 and the sulfur/chlorine compounds were determined, and the effects of temperature and the main components in flue gases were studied. The gas phase reaction between Hg0 and SCl2 is shown to be more rapid than the gas phase reaction with chlorine, and the second order rate constant was 9.1(+-0.5) x 10-18 mL-molecules-1cdots-1 at 373oK. Nitric oxide (NO) inhibited the gas phase reaction of Hg0 with sulfur-chlorine compounds. The presence of flyash or powdered activated carbon in flue gas can substantially accelerate the reaction. The predicted Hg0 removal is about 90percent with 5 ppm SCl2 or S2Cl2 and 40 g/m3 of flyash in flue gas. The combination of activated carbon and sulfur-chlorine compounds is an effective alternative. We estimate that co-injection of 3-5 ppm of SCl2 (or S2Cl2) with 2-3 Lb/MMacf of untreated Darco-KB is comparable in efficiency to the injection of 2-3 Lb/MMacf Darco-Hg-LH. Extrapolation of kinetic results also indicates that 90percent of Hg0 can be removed if 3 Lb/MMacf of Darco-KB pretreated with 3percent of SCl2 or S2Cl2 is used. Unlike gas phase reactions, NO exhibited little effect on Hg0 reactions with SCl2 or S2Cl2 on flyash or activated carbon. Mercuric sulfide was identified as one of the principal products of the Hg0/SCl2 or Hg0/S2Cl2 reactions. Additionally, about 8percent of SCl2 or S2Cl2 in aqueous solutions is converted to sulfide ions, which would precipitate mercuric ion from FGD solution.

  10. Transformation of chlorine in NaCl-loaded Victorian brown coal during the gasification in steam

    Institute of Scientific and Technical Information of China (English)

    ZHANG Shu; Mohammad Asadullah; Rosalie Hocking; LIN Jian-ying; LI Chun-zhu

    2012-01-01

    This study is to examine the changes in Cl volatilizations and chemical forms in NaCl-loaded Victorian brown coal during gasification in steam at 800 ℃ using Cl K-edge X-ray absorption near-edge structure (XANES) spectroscopy.The char samples were prepared in a novel one-stage fluidised-bed/fixed-bed quartz reactor at a fast heating rate.The samples were then collected and sealed in an argon-filled bag in order to minimise possible oxidation of char and Cl by air prior to analysis by XANES.Char-steam reactions were found to significantly affect the transformation of Cl,including the possible formation of chlorine-containing organic structures.On the other hand,volatile-char interactions during the gasificauon appeared to enhance the Cl retention and prevent the formation of organic chlorine compounds in chars.

  11. Kinetic modelling of chlorination of nitrided ilmenite using MATLAB

    Science.gov (United States)

    Ramakrishnan, Sivakumar; Kwok, Teong Chen; Hamid, Sheikh Abdul Rezan Sheikh Abdul

    2016-07-01

    In the present study, chlorination of nitride ilmenite using 2k factorial design was investigated. The reduction experiments were carried out in a temperature range of 400°C to 500°C, chlorination duration from 1 hour to 3 hours and using different type of carbon reactant. Phases of raw materials and reduced samples were analyzed by X-ray diffraction (XRD). Ilmenite was reduced to TiOxCyNz through carbothermal and nitridation for further chlorination into titanium tetrachloride. The Design of Experiment analysis suggested that the types of carbon reactant contribute most influence to the extent of chlorination of nitride ilmenite. The extent of chlorination was highest at 500°C with 3 hours chlorination time and carbon nanotube as carbon reactant.

  12. Cyclopalladated Ferrocenylimine Catalyzed Chlorination of 2-Arylbenzoxazoles%Cyclopalladated Ferrocenylimine Catalyzed Chlorination of 2-Arylbenzoxazoles

    Institute of Scientific and Technical Information of China (English)

    冷瑜婷; 杨帆; 吴养洁; 李克

    2011-01-01

    An efficient and facile protocol for palladacycle-catalyzed chlorination of 2-arylbenzoxazoles was developed. The results represent the first examples involving the palladacycle as the catalyst for such chlorination. This chlori- nation was not a ligand-directed ortho-C--H activation, but an electrophilic substitution process at the para-position of the nitrogen atom in the benzo ring of benzoxazole moiety, the regiochemistry of which had been confirmed by HMBC spectral analysis. The catalytic system could tolerate various halogen atoms, such as F, Cl and Br, affording the corresponding products in moderate to excellent yields.

  13. The use of chlorine dioxide for zebra mussel control - A perspective of treatment histories

    Energy Technology Data Exchange (ETDEWEB)

    Smolik, N.; Rusznak, L.; Anderson, J.; Hale, L. [Ashland Chemical Coman, Drew Division, Booton, NJ (United States)

    1995-06-01

    It is of utmost importance to provide updated performance results of various chemical treatments presently being utilized for zebra mussel control. Zebra mussels have a distinctive ability to endure environmental changes by reproducing effectively and attaching to various hard surfaces. These traits are cause for concern and have resulted in some operating difficulties for industries bordering infested waterways. Various methods are being employed by industries to deal with the problems associated with these species. One of the options is control via chemical treatment. Prior field test studies showed that chlorine dioxide was determined to be an effective molluscicidal agent for adult zebra mussel eradication. Continuous feed of chlorine dioxide at treatment levels ranging from 0.25 - 5.0 ppm above the oxidant demand provided 100% adult zebra mussel mortality which required between 2.9 - 8.8 days of treatment. Previous studies also showed that water temperature was an essential parameter in determining the time required to achieve 100% mortality of adult zebra mussels. Further field applications were undertaken at three electric utility sites located in the midwest. These facilities were concerned with the potential for zebra mussels to reduce efficiency and availability by blocking water flow or plugging equipment. Treatment applications at these facilities consisted of a continuous feed of chlorine dioxide ranging from 0.15 - 0.5 ppm above the oxidant demand. Significant mortality was achieved in monitored mussels tested at each utility in a period ranging from two to four days. This time period was directly related to a number of parameters, with the predominant one being water temperature. Data from these field applications is presented in this paper and confirms that chlorine dioxide is an effective molluscicide for adult zebra mussel control.

  14. The removal of phenols from oily wastewater by chlorine dioxide

    OpenAIRE

    Hsu, Chung-Jung

    1988-01-01

    Treatability studies were performed on oily wastewaters produced by petroleum and canning industries. Chlorine dioxide was used for the removal of phenolic compounds from these oily wastewaters. Most of phenolic compounds can be destroyed by chlorine dioxide within 15 minutes if CI02-to-phenol ratios of higher than 5.0 are provided. Factors such as pH, temperature, and COD have little effect on phenol removal. The effectiveness of chlorine dioxide treatment depends critic...

  15. Blends of caprolactam/caprolactone copolymers and chlorinated polymers

    OpenAIRE

    Alberda van Ekenstein, G.O.R.; Deuring, H.; ten Brinke, G.; Ellis, T. S.

    1997-01-01

    The phase behaviour of blends of chlorinated polyethylene, polyvinyl chloride (PVC) and chlorinated PVC with random copolymers of caprolactone and caprolactam has been investigated and the results correlated with a binary interaction model. The known miscibility of polycaprolactone in the chlorinated polymers is not compromised until a relatively high lactam content in the copolymer is attained. The incorporation of segmental interaction parameters, derived from separate studies involving pol...

  16. Biochars made from agro-industrial by-products remove chlorine and lower water toxicity

    Science.gov (United States)

    Tzachristas, Andreas; Xirou, Maria; Manariotis, Ioannis D.; Dailianis, Stefanos; Karapanagioti, Hrissi K.

    2016-04-01

    Chlorination is the most common disinfection process for water and treated wastewater. For the industrial use of water in food production, chlorine can add undesired taste and odor to the final product. For this reason, dechlorination is desired for food industries that use municipal tap water. For treated wastewater discharge or reuse, chlorine can be toxic to the receiving aqueous systems and to the irrigated plants. In both the above cases, dechlorination is also required. Traditionally activated carbon has been used as the ideal material for the removal of chlorine. The main mechanisms that describe the interaction between activated carbon and HOCl or OCl- are described by the following equations (AWWA, 1990): HOCl + C* → C*O + H+ + Cl- (1), OCl- + C* → C*O + Cl- (2) Where C* and C*O represent the activated carbon surface and a surface oxide, respectively. The present study proposes the use of agro-industrial by-products for the production of biochars that will be used for dechlorination of tap-water used for food-industry production. Different raw materials such as malt spent rootlets, coffee residue, olive and grape seeds, etc. are used for the production of biochar. Various temperatures and air-to-solid ratios are tested for optimizing biochar production. Batch tests as well as a column test are employed to study the dechlorination efficiency and kinetics of the different raw and biochar materials as well as those of commercial activated carbons. As chlorine concentration increases the removal also increases linearily. After 1 and 24 hours of contact the chlorine relative removal efficiencies for the biochar made from olive seeds are 50 and 77 ± 4%, respectively. It seems that the removal kinetics are faster during the first hour; then, removal continues but with a slower rate. Most of the biochars tested (with 3 mg of solid in 20 mL of chlorine solution at initial concentration Co=1.5 mg/L) demonstrated removal efficiencies with an average of 9.4 ± 0

  17. Mechanisms of inactivation of poliovirus by chlorine dioxide and iodine.

    OpenAIRE

    Alvarez, M E; O'Brien, R T

    1982-01-01

    Chlorine dioxide and iodine inactivated poliovirus more efficiently at pH 10.0 than at pH 6.0. Sedimentation analyses of viruses inactivated by chlorine dioxide and iodine at pH 10.9 showed that viral RNA separated from the capsids, resulting in the conversion of virions from 156S structures to 80S particles. The RNAs release from both chlorine dioxide- and iodine-inactivated viruses cosedimented with intact 35S viral RNA. Both chlorine dioxide and iodine reacted with the capsid proteins of p...

  18. Effects of UV irradiation and UV/chlorine co-exposure on natural organic matter in water

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Wei; Zhang, Zaili; Yang, Xin; Xu, Yiyue; Liang, Yongmei, E-mail: liangym@mail.sysu.edu.cn

    2012-01-01

    The effects of co-exposure to ultraviolet (UV) irradiation (with either low- or medium-pressure UV lamps) and free chlorine (chloramine) at practical relevant conditions on changes in natural organic matter (NOM) properties were investigated using four waters. The changes were characterized using the specific disinfection by-product formation potential (SDBPFP), specific total organic halogen formation potential (STOXFP), differential UV absorbance ( Increment UVA), and size-exclusion chromatography (SEC). The results for exposure to UV irradiation alone and for samples with no exposure were also obtained. The SDBPFPs in all UV-irradiated NOM waters observed were higher than those of non-irradiated samples. UV irradiation led to increases in STOXFPs as a result of chlorination, but no changes, or only small decreases, from chloramination. UV irradiation alone led to positive Increment UVA spectra of the four NOM waters; co-exposure to UV and chlorine gave larger negative Increment UVA spectra than those obtained by chlorine exposure alone. No obvious changes in SEC results were observed for samples only irradiated with UV light; co-exposure gave no detectable changes in the abundances of small fractions for exposure to chlorine only. Both UV photooxidation and photocatalytic oxidation appear to affect the reactivity of the NOM toward subsequent chlorination, and the magnitude of the changes is generally greater for medium-pressure lamps than for low-pressure lamps. These results suggest that applying UV disinfection technology to a particular source may not always be disinfection by-product-problem-free, and the interactions between UV light, chlorine, and NOM may need to be considered. - Highlights: Black-Right-Pointing-Pointer We discussed the effects of co-exposure to UV light and chlorine on properties of natural organic matters in waters. Black-Right-Pointing-Pointer UV irradiation led to increases in SDBPFP and STOXFP of NOM waters from chlorination. Black

  19. Peroxone activated persulfate treatment of 1,4-dioxane in the presence of chlorinated solvent co-contaminants.

    Science.gov (United States)

    Eberle, Dylan; Ball, Raymond; Boving, Thomas B

    2016-02-01

    1,4-dioxane is often found as a co-contaminant with chlorinated volatile organic compounds (VOCs) at solvent release sites such as landfills, solvent recycling facilities, or fire training areas. Historically, soil and groundwater samples were not routinely analyzed for 1,4-dioxane and therefore the number of known 1,4-dioxane sites is still increasing. Due to its co-occurrence with chlorinated compounds, remediation strategies are needed that simultaneously treat both 1,4-dioxane as well as chlorinated VOC co-contaminants. In this proof of concept laboratory study, the fate of 1,4-dioxane was examined during the targeted destruction of aqueous phase VOC, using a peroxone activated persulfate (PAP) chemical oxidation method. Bench-scale experiments were carried out to evaluate the treatability of 1,4-dioxane as both a single-contaminant and in the presence of trichloroethene (TCE), and 1,1,1-trichloroethane (1,1,1-TCA). Possible dependencies on oxidant concentration and reaction kinetics were studied. The oxidative destruction of 1,4-dioxane, TCE and 1,1,1-TCA in single-contaminant batch systems followed pseudo-first-order reaction kinetics and even at the most dilute oxidant concentration lasted for at least 13 days. The rate of oxidation for each contaminant increased linearly with increasing persulfate concentration over the range of oxidant concentrations tested. The rate of oxidative destruction, from most easily degraded to least, was: TCE > 1,4-dioxane > 1,1,1-TCA. Oxidation rates were up to 87% slower in a mixture of these three compounds. Although additional tests are necessary, our data suggest that PAP oxidation of 1,4-dioxane might aid in the cleanup of VOC contaminated sites. PMID:26408980

  20. Scenarios Evaluation Tool for Chlorinated Solvent MNA

    Energy Technology Data Exchange (ETDEWEB)

    Vangelas, Karen; Michael J. Truex; Charles J. Newell; Brian Looney

    2007-02-28

    Over the past three decades, much progress has been made in the remediation of chlorinated solvents from the subsurface. Yet these pervasive contaminants continue to present a significant challenge to the U.S. Department of Energy (DOE), other federal agencies, and other public and private organizations. The physical and chemical properties of chlorinated solvents make it difficult to rapidly reach the low concentrations typically set as regulatory limits. These technical challenges often result in high costs and long remediation time frames. In 2003, the DOE through the Office of Environmental Management funded a science-based technical project that uses the U.S. Environmental Protection Agency's technical protocol (EPA, 1998) and directives (EPA, 1999) on Monitored Natural Attenuation (MNA) as the foundation on which to introduce supporting concepts and new scientific developments that will support remediation of chlorinated solvents based on natural attenuation processes. This project supports the direction in which many site owners want to move to complete the remediation of their site(s), that being to complete the active treatment portion of the remedial effort and transition into MNA. The overarching objective of the effort was to examine environmental remedies that are based on natural processes--remedies such as Monitored Natural Attenuation (MNA) or Enhanced Attenuation (EA). The research program did identify several specific opportunities for advances based on: (1) mass balance as the central framework for attenuation based remedies, (2) scientific advancements and achievements during the past ten years, (3) regulatory and policy development and real-world experience using MNA, and (4) exploration of various ideas for integrating attenuation remedies into a systematic set of ''combined remedies'' for contaminated sites. These opportunities are summarized herein and are addressed in more detail in referenced project documents and

  1. The Potential Feasibility of Chlorinic Photosynthesis on Extrasolar Planets

    Science.gov (United States)

    Haas, Johnson

    2009-09-01

    It is highly likely that the first convincing evidence of extrasolar life will arrive in the form of atmospheric absorption spectra. The modern search for life-bearing extrasolar planets emphasizes the potential detection of O2 and O3 absorption spectra in exoplanetary atmospheres as archetypal signatures of biology. However, oxygenic photosynthesis apparently failed to evolve independently more than once on Earth, and is thus unlikely to be reliably ubiquitous throughout the universe. Alternative evolutionary paths may yield planetary atmospheres tinted with the waste products of other dominant metabolisms, including potentially exotic biochemistries. This study examines the potential feasibility of one such exotic metabolism: chlorinic photosynthesis (CPS), defined as biologically-mediated halogenation of aqueous chloride to HClO, Cl2 or partially-oxidized intermediates (e.g. haloalkanes, haloacids, haloaromatics), coupled with photosynthetic CO2 fixation. This metabolic couple is feasible thermodynamically and appears to be geochemically plausible under approximately terrestrial conditions. This study hypothesizes that planetary biospheres dominated by CPS would develop atmospheres enriched with dihalogens and other halogenated compounds, evolve a highly oxidizing surface geochemical environment, and foster biological selection pressures favoring halogen resistance and eventual metazoan heterotrophy based on dihalogen and halocarbon respiration. Planets favoring the evolution of CPS would probably receive equivalent or greater surface UV flux than Earth did in the Paleoarchean (promoting abiotic photo-oxidation of aqueous halides, and establishing a strong biological selective pressure toward their accommodation), and would orbit stars having equivalent or greater bulk metallicities (promoting greater planetary halide abundances) relative to the Sun. Directed searches for such worlds should probably focus on A, F and G0 spectral class stars having bulk

  2. Structural changes and dynamic behaviour of vanadium oxide-based catalysts for gas-phase selective oxidations

    OpenAIRE

    Luciani, Silvia

    2009-01-01

    Selective oxidation is one of the simplest functionalization methods and essentially all monomers used in manufacturing artificial fibers and plastics are obtained by catalytic oxidation processes. Formally, oxidation is considered as an increase in the oxidation number of the carbon atoms, then reactions such as dehydrogenation, ammoxidation, cyclization or chlorination are all oxidation reactions. In this field, most of processes for the synthesis of important chemicals used vanadium oxide-...

  3. Development of RuO2/TiO2 titanium anodes and a device for in situ active chlorine generation

    Directory of Open Access Journals (Sweden)

    Spasojević Miroslav D.

    2013-01-01

    Full Text Available Chlorine is used worldwide for water disinfection purposes. However, due to its toxicity the EU has imposed a set of standards that must be applied when transporting and storing chlorine. In Serbia, numerous studies have been conducted attempting to develop the technology for the generation of active chlorine disinfectant but with a non-toxic aqueous solution of sodium chloride as the raw material. This study provides an overview of the titanium anodes activated by thermally obtained solid solution of ruthenium and titanium oxide development. It also presents new findings on the effect of the temperature of thermal treatment, the composition, the thickness of an active coating on its microstructural properties, and consequently on the catalytic activity, ion selectivity, and corrosion stability during active chlorine generation through the electrolysis of dilute sodium chloride solutions at room temperature. The study also evaluates the effect of the kinetic and operational parameters of the electrochemical process of active chlorine generation on both current and energy efficiencies. The results obtained were used to determine optimal values of technological parameters of the production process. This comprehensive research resulted in the construction of different types of remote-controlled and fully automated active chlorine generating plants.

  4. Chlorine gas inhalation: human clinical evidence of toxicity and experience in animal models.

    Science.gov (United States)

    White, Carl W; Martin, James G

    2010-07-01

    inhalation have demonstrated evidence of oxidative injury and inflammation. Early epithelial injury, airways hyperresponsiveness, and airway remodeling, likely diminishing over time, have been shown. As in humans, ALI/ARDS can occur, becoming more likely when the upper airways are bypassed. Inhalation models of chlorine toxicity provide unique opportunities for testing potential pharmacologic rescue agents. PMID:20601629

  5. UASB reactor effluent disinfection by ozone and chlorine

    NARCIS (Netherlands)

    Ribeiro da Silvia, G.H.; Bruning, H.; Gerrity, D.; Daniel, L.A.

    2015-01-01

    This research studied the sequential ozone and chlorine process with respect to, the inactivation of indicator bacteria and the formation of ozone disinfection byproducts in sanitary wastewater effluent. The applied ozone doses were 5, 8 and 10 mg.O3.L-1, followed by chlorine doses of 10, 20 and 30

  6. Chlorine Dioxide Induced Multiple Chemical Sensitivity: MMPI Validity Problems.

    Science.gov (United States)

    Tentoni, Stuart C.

    This paper discusses Minnesota Multiphasic Personality Inventory (MMPI) data obtained from individuals exposed to chlorine dioxide in the workplace who developed Multiple Chemical Sensitivity Syndrome. The paper explores current research on chlorine dioxide exposed persons who were misdiagnosed on the basis of MMPI interpretations. Difficulties…

  7. 78 FR 66767 - Chlorinated Isocyanurates From China and Japan

    Science.gov (United States)

    2013-11-06

    ... publishing the notice in the Federal Register of September 10, 2013 (78 FR 55293). The conference was held in... COMMISSION Chlorinated Isocyanurates From China and Japan Determinations On the basis of the record \\1... injured by reason of imports from China and Japan of chlorinated isocyanurates, provided for...

  8. Chlorine-containing natural compounds in higher plants

    DEFF Research Database (Denmark)

    Engvild, Kjeld Christensen

    1986-01-01

    More than 130 chlorine-containing compounds have been isolated from higher plants and ferns; about half are polyacetylenes, thiophenes and sesquiterpene lactones from the Asteraceae. A chlorinated chlorophyll may be an important part of photosystem 1. High biological activity is found in 4...

  9. INVESTIGATION OF INTERMITTENT CHLORINATION SYSTEM IN BIOLOGICAL EXCESS SLUDGE REDUCTION BY SEQUENCING BATCH REACTORS

    Directory of Open Access Journals (Sweden)

    A. Takdastan ، N. Mehrdadi ، A. A. Azimi ، A. Torabian ، G. Nabi Bidhendi

    2009-01-01

    Full Text Available The excessive biological sludge production is one of the disadvantages of aerobic wastewater treatment processes such as sequencing batch reactors. To solve the problem of excess sludge production, oxidizing some of the sludge by chlorine, thus reducing the biomass coefficient as well as the sewage sludge disposal may be a suitable idea. In this study, two sequencing batch reactors, each with 20 L volume and controlled by on-line system were used. After providing the steady state conditions in the reactors, sampling and testing of parameters were done during 8 months. The results showed that during the solid retention time of 10 days the kinetic coefficient of Y and Kd were 0.58 mg biomass/mg COD and 0.058/day, respectively. At the next stage, different concentrations of chlorine were used in the reactors intermittently. Results showed that 15 mg chlorine/gMLSS in the reactor was able to reduce the yield coefficient from 0.58 to 0.3 mg biomass/mg COD. In other words, the biological excess sludge was reduced about 48%. But the soluble chemical oxygen demand increased slightly in the effluent and the removal percentage decreased from 95% in the blank reactor to 55% in the test reactor.

  10. Reducing the chlorine dioxide demand in final disinfection of drinking water treatment plants using activated carbon.

    Science.gov (United States)

    Sorlini, Sabrina; Biasibetti, Michela; Collivignarelli, Maria Cristina; Crotti, Barbara Marianna

    2015-01-01

    Chlorine dioxide is one of the most widely employed chemicals in the disinfection process of a drinking water treatment plant (DWTP). The aim of this work was to evaluate the influence of the adsorption process with granular activated carbon (GAC) on the chlorine dioxide consumption in final oxidation/disinfection. A first series of tests was performed at the laboratory scale employing water samples collected at the outlet of the DWTP sand filter of Cremona (Italy). The adsorption process in batch conditions with seven different types of GAC was studied. A second series of tests was performed on water samples collected at the outlet of four GAC columns installed at the outlet of the DWTP sand filter. The results showed that the best chlorine dioxide demand (ClO2-D) reduction yields are equal to 60-80% and are achieved in the first 30 min after ClO2 addition, during the first 16 days of the column operation using a mineral, coal-based, mesoporous GAC. Therefore, this carbon removes organic compounds that are more rapidly reactive with ClO2. Moreover, a good correlation was found between the ClO2-D and UV absorbance at wavelength 254 nm using mineral carbons; therefore, the use of a mineral mesoporous GAC is an effective solution to control the high ClO2-D in the disinfection stage of a DWTP. PMID:25465650

  11. Parallel oxygen and chlorine evolution on Ru1-xNixO2-y nanostructured electrodes

    International Nuclear Information System (INIS)

    Nanocrystalline materials with chemical composition corresponding to formula Ru1-xNixO2-y (0.02 1-xNixO2-y with respect to parallel oxygen (oxygen evolution reaction, OER) and chlorine (chlorine evolution reaction, CER) evolution in acidic media was studied by voltammetry combined with differential electrochemical mass spectrometry (DEMS). The DEMS data indicate a significant decrease of the over-voltage for chlorine evolution with respect to that of pure RuO2. The oxygen evolution is slightly hindered. The increasing Ni content affects the electrode material activity and selectivity. The overall material's activity increases with increasing Ni content. The activity of the Ru-Ni-O oxides towards Cl2 evolution shows a distinguished maximum for material containing 10% of Ni. Further increase of Ni content results in suppression of Cl2 evolution in favor of O2 evolution. A model reflecting the cation-cation interactions resulting from Ni-doping is proposed to explain the observed trends in electrocatalytic behavior

  12. Performance of an anaerobic, static bed, fixed film bioreactor for chlorinated solvent treatment

    Science.gov (United States)

    Lorah, Michelle M.; Walker, Charles; Graves, Duane

    2015-01-01

    Anaerobic, fixed film, bioreactors bioaugmented with a dechlorinating microbial consortium were evaluated as a potential technology for cost effective, sustainable, and reliable treatment of mixed chlorinated ethanes and ethenes in groundwater from a large groundwater recovery system. Bench- and pilot-scale testing at about 3 and 13,500 L, respectively, demonstrated that total chlorinated solvent removal to less than the permitted discharge limit of 100 μg/L. Various planned and unexpected upsets, interruptions, and changes demonstrated the robustness and reliability of the bioreactor system, which handled the operational variations with no observable change in performance. Key operating parameters included an adequately long hydraulic retention time for the surface area, a constant supply of electron donor, pH control with a buffer to minimize pH variance, an oxidation reduction potential of approximately −200 millivolts or lower, and a well-adapted biomass capable of degrading the full suite of chlorinated solvents in the groundwater. Results indicated that the current discharge criteria can be met using a bioreactor technology that is less complex and has less downtime than the sorption based technology currently being used to treat the groundwater.

  13. [Aspartic Acid Generated in the Process of Chlorination Disinfection By-product Dichloroacetonitrile].

    Science.gov (United States)

    Ding, Chun-sheng; Li, Nai-jun; Zhang, Tao; Zhang, Meng-qing

    2016-05-15

    In this study, a method was developed for the determination of dichloroacetonitrile (DCAN) in drinking water by liquid- liquid micro-extraction and gas chromatography/mass spectrometry ( LLE-GC/MS), which used 1,2-dibromopropane as the internal standard and methyl tertiary butyl ether (MTBE) as the extractant for high accuracy. The aspartic acid was used as the precursor of the DCAN formation during chlorination and the influencing factors were evaluated. The formation mechanism of DCAN was also discussed. The results showed that the DCAN amount increased with the increase of pH value under the neutral and acidic conditions, however, the amount of DCAN decreased with the increase of pH value under the alkali condition. And the final amount of DCAN under the alkali condition was much less than that under the neutral and acidic conditions. It was also found that the DCAN amount increased with the increase of chlorine addition, while the temperature in the range of 10-30°C had little influence on the DCAN formation. The formation process of the DCAN from aspartic acid by chlorination included seven steps, such as substitution, decarboxylation, oxidation, etc and ultimately formed DCAN. PMID:27506037

  14. [Aspartic Acid Generated in the Process of Chlorination Disinfection By-product Dichloroacetonitrile].

    Science.gov (United States)

    Ding, Chun-sheng; Li, Nai-jun; Zhang, Tao; Zhang, Meng-qing

    2016-05-15

    In this study, a method was developed for the determination of dichloroacetonitrile (DCAN) in drinking water by liquid- liquid micro-extraction and gas chromatography/mass spectrometry ( LLE-GC/MS), which used 1,2-dibromopropane as the internal standard and methyl tertiary butyl ether (MTBE) as the extractant for high accuracy. The aspartic acid was used as the precursor of the DCAN formation during chlorination and the influencing factors were evaluated. The formation mechanism of DCAN was also discussed. The results showed that the DCAN amount increased with the increase of pH value under the neutral and acidic conditions, however, the amount of DCAN decreased with the increase of pH value under the alkali condition. And the final amount of DCAN under the alkali condition was much less than that under the neutral and acidic conditions. It was also found that the DCAN amount increased with the increase of chlorine addition, while the temperature in the range of 10-30°C had little influence on the DCAN formation. The formation process of the DCAN from aspartic acid by chlorination included seven steps, such as substitution, decarboxylation, oxidation, etc and ultimately formed DCAN.

  15. Reducing the chlorine dioxide demand in final disinfection of drinking water treatment plants using activated carbon.

    Science.gov (United States)

    Sorlini, Sabrina; Biasibetti, Michela; Collivignarelli, Maria Cristina; Crotti, Barbara Marianna

    2015-01-01

    Chlorine dioxide is one of the most widely employed chemicals in the disinfection process of a drinking water treatment plant (DWTP). The aim of this work was to evaluate the influence of the adsorption process with granular activated carbon (GAC) on the chlorine dioxide consumption in final oxidation/disinfection. A first series of tests was performed at the laboratory scale employing water samples collected at the outlet of the DWTP sand filter of Cremona (Italy). The adsorption process in batch conditions with seven different types of GAC was studied. A second series of tests was performed on water samples collected at the outlet of four GAC columns installed at the outlet of the DWTP sand filter. The results showed that the best chlorine dioxide demand (ClO2-D) reduction yields are equal to 60-80% and are achieved in the first 30 min after ClO2 addition, during the first 16 days of the column operation using a mineral, coal-based, mesoporous GAC. Therefore, this carbon removes organic compounds that are more rapidly reactive with ClO2. Moreover, a good correlation was found between the ClO2-D and UV absorbance at wavelength 254 nm using mineral carbons; therefore, the use of a mineral mesoporous GAC is an effective solution to control the high ClO2-D in the disinfection stage of a DWTP.

  16. Biodegradability of Chlorinated Anilines in Waters

    Institute of Scientific and Technical Information of China (English)

    CHAO WANG; GUAN-GHUA LU; YAN-JIE ZHOU

    2007-01-01

    Objective To identify the bacteria tolerating chlorinated anilines and to study the biodegradability of o-chloroaniline and its coexistent compounds. Methods Microbial community of complex bacteria was identified by plate culture observation techniques and Gram stain method. Bacterial growth inhibition test was used to determine the tolerance of complex bacteria to toxicant. Biodegradability of chlorinated anilines was determined using domesticated complex bacteria as an inoculum by shaking-flask test. Results The complex bacteria were identified, consisting of Xanthomonas, Bacillus alcaligenes,Acinetobacter, Pseudomonas, and Actinomycetaceae nocardia. The obtained complex bacteria were more tolerant to o-chloroaniline than mixture bacteria in natural river waters. The effects of exposure concentration and inoculum size on the biodegradability of o-chloroaniline were analyzed, and the biodegradation characteristics of single o-chloroaniline and 2,4-dichloroaniline were compared with the coexistent compounds. Conclusion The biodegradation rates can be improved by decreasing concentration of compounds and increasing inoculum size of complex bacteria. When o-chloroaniline coexists with aniline, the latter is biodegraded prior to the former, and as a consequence the metabolic efficiency of o-chloroaniline is improved with the increase of aniline concentration. Meanwhile, when o-chloroaniline coexists with 2,4-dichloroaniline, the metabolic efficiency of 2,4-dichloroaniline is markedly improved.

  17. Low-Cost Graphite-Based Free Chlorine Sensor.

    Science.gov (United States)

    Pan, Si; Deen, M Jamal; Ghosh, Raja

    2015-11-01

    Pencil lead was used to fabricate a graphite-based electrode for sensing applications. Its surface was electrochemically modified using ammonium carbamate to make it suitable for sensing free chlorine in water samples. Chlorine is widely used as a disinfectant in the water industry, and the residual free chlorine concentration in water distributed to the consumers must be lower than that stipulated by regulatory bodies. The graphite-based amperometric sensor gave a selective and linear response to free chlorine in the relevant concentration range and no response to commonly interfering ions. It was evaluated further for storage stability, response time, and hysteresis. This sensor is being proposed as a low-cost device for determining free chlorine in water samples. Its ease-of-use, limitations, and feasibility for mass-production and application is discussed.

  18. Reactive chlorine chemistry in the boundary layer of coastal Antarctica

    Science.gov (United States)

    Zielcke, Johannes; Poehler, Denis; Friess, Udo; Hay, Tim; Eger, Philipp; Kreher, Karin; Platt, Ulrich

    2015-04-01

    A unique feature of the polar troposphere is the strong impact of halogen photochemistry, in which reactive halogen species are responsible for ozone depletion as well as the oxidation of elemental mercury and dimethyl sulphide. The source, however, as well as release and recycling mechanisms of these halogen species - for some species even abundances - are far from being completely known, especially of chlorine and iodine compounds. Here we present active long-path differential optical absorption spectroscopy (LP-DOAS) measurements conducted during austral spring 2012 at Ross Island, Antarctica, observing several species (BrO, O3, NO2, IO, ClO, OBrO, OClO, OIO, I2, CHOCHO, HCHO, HONO). For the first time, ClO was detected and quantified in the marine boundary layer of coastal Antarctica, with typical mixing ratios around 20 pptv and maxima around 50 pptv. Meteorological controls on the mixing ratio of ClO as well as the interplay with other halogen compounds will be discussed, such as the lack of observed OClO (< 1 pptv). The results seem to reflect previously in chamber studies observed dependences on ozone levels and solar irradiance.

  19. Degradation of chlorinated phenols by nanoscale zero-valent iron

    Institute of Scientific and Technical Information of China (English)

    Rong CHENG; Jianlong WANG; Weixian ZHANG

    2008-01-01

    Chlorophenols (CPs), as important contami-nants in groundwater, are toxic and difficult to biode-grade. Recently nanoscale zero-valent iron received a great deal of attention because of its excellent performance in treating recalcitrant compounds. In this study, nanoscale zero-valent iron particles were prepared using chemical reduction, and the reductive transformations of three kinds of chlorinated phenols (2-CP, 3-CP, and 4-CP) by nanoscale zero-valent iron under different conditions were investigated. The transformation process of the CPs was shown to be dechlorination first, then cleavage of the benzene ring. The removal efficiency of the CPs varied as follows: 2-CP3-CP4-CP. The reactivity of CPs was associated with their energy of lowest unoccupied molecular orbit (ELUMO). With the increase in initial concentrations of CPs, removal efficiency decreased a little. But the quantities of CPs reduced increased evidently. Temperature had influence on not only the removal efficiency, but also the transformation pathway. At higher temperatures, dechlorination occurred prior to benzene ring cleavage. At lower temperatures, however, the oxidation product was formed more easily.

  20. The Dutch secret: how to provide safe drinking water without chlorine in the Netherlands

    Directory of Open Access Journals (Sweden)

    G. J. Medema

    2009-03-01

    Full Text Available The Netherlands is one of the few countries where chlorine is not used at all, neither for primary disinfection nor to maintain a residual disinfectant in the distribution network. The Dutch approach that allows production and distribution of drinking water without the use of chlorine while not compromising microbial safety at the tap, can be summarized as follows:
    1. Use the best source available, in order of preference:
        – microbiologically safe groundwater,
        – surface water with soil passage such as artificial recharge or bank filtration,
        – direct treatment of surface water in a multiple barrier treatment;
    2. Use a preferred physical process treatment such as sedimentation, filtration and UV-disinfection. If absolutely necessary, also oxidation by means of ozone or peroxide can be used, but chlorine is avoided;
    3. Prevent ingress of contamination during distribution;
    4. Prevent microbial growth in the distribution system by production and distribution of biologically stable (biostable water and the use of biostable materials;
    5. Monitor for timely detection of any failure of the system to prevent significant health consequences.

    New developments in safe drinking water in the Netherlands include the adaptation of the Dutch drinking water decree, implementation of quantitative microbial risk assessment (QMRA by water companies and research into source water quality, drinking water treatment efficacy, safe distribution and biostability of drinking water during distribution and Legionella. This paper summarizes how the Dutch water companies warrant the safety of the drinking water without chlorine.

  1. The Dutch secret: safe drinking water without chlorine in the Netherlands

    Directory of Open Access Journals (Sweden)

    J. C. van Dijk

    2008-10-01

    Full Text Available The Netherlands is one of the few countries where chlorine is not used at all, neither for primary disinfection nor to maintain a residual disinfectant in the distribution network. The Dutch approach that allows production and distribution of drinking water without the use of chlorine while not compromising microbial safety at the tap, can be summarized as follows:

    1. Use the best source available, in order of preference:
      – microbiologically safe groundwater,
      – surface water with soil passage such as artificial recharge or bank filtration,
      – direct treatment of surface water in a multiple barrier treatment;
    2. Use a preferred physical process treatment such as sedimentation, filtration and UV-disinfection. If absolutely necessary, also oxidation by means of ozone or peroxide can be used, but chlorine is avoided;
    3. Prevent ingress of contamination during distribution;
    4. Prevent microbial growth in the distribution system by production and distribution of biologically stable (biostable water and the use of biostable materials;
    5. Monitor for timely detection of any failure of the system to prevent significant health consequences.
    New developments in safe drinking water in the Netherlands include the adaptation of the Dutch drinking water decree, implementation of quantitative microbial risk assessment (QMRA by water companies and research into source water quality, drinking water treatment efficacy, safe distribution and biostability of drinking water during distribution and extit{Legionella}. This paper summarizes how the Dutch water companies warrant the safety of the drinking water without chlorine.

  2. Demonstration of denitration and chlorination process using real high level liquid waste

    International Nuclear Information System (INIS)

    The pyropartitioning process separates the actinide elements including the minor actinide elements from the high-level liquid waste generated at the Purex reprocessing of spent LWR fuel and introduces them to metallic fuel cycle. Since the separation of the actinide elements from the fission product elements is performed in molten chloride salt/liquid metal system, the actinide and fission product elements in the high-level liquid waste must be converted to the chlorides as the first step of the pyropartitioning process. In order to demonstrate the conversion of the actinide and fission product elements to the chlorides, a series of denitration and chlorination test using 520g of real high-level liquid waste, which contains 8400 micro-g/g of uranium, 600 micro-g/g of transuranium elements, and 2000 micro-g/g of fission products including 870 micro-g/g of rare-earth elements, was performed. The results of the tests are as following; 1) The entire denitration product of the high-level liquid waste was successfully recovered from the containing crucible, which is made of stainless steel. No damage was found on the inside surface of the crucible. During the denitration, small amount of ruthenium was evaporated. 2) After the chlorination of the denitrated material, only 1 to 5% of each actinide element remained as the water insoluble material in the salt phase, which is assumed to be oxide. And almost all of the actinide elements were converted to water soluble material in the salt phase, which are assumed to be chloride. Additionally, almost all of the rare-earth fission product, alkaline-earth fission product, and alkaline-metal fission product elements were also converted to water soluble material in the salt. Some of the fission products such as molybdenum and zirconium were evaporated during the chlorination. 3) Since nearly 100% of each actinide element was recovered as the chloride, the denitration and chlorination were successfully demonstrated. (author)

  3. Recovering Y and Eu from Waste Phosphors Using Chlorination Roasting—Water Leaching Process

    Directory of Open Access Journals (Sweden)

    Mingming Yu

    2016-10-01

    Full Text Available Recovering Y and Eu from waste phosphors using chlorination roasting followed by a water leaching process was investigated in this study. Firstly, by chlorination roasting and water leaching, Y and Eu elements present in waste phosphors were efficiently extracted into a leach solution. Secondly, the majority of the impurities in the solution can be removed by adjusting the pH to 4.5 using a Na2S and NH3·H2O solution. Thirdly, the rare earths can be precipitated afterwards by adding a H2C2O4 solution and adjusting the pH to 2.0. Then rare earth oxides (REOs can be obtained after calcining at 800 °C for 1 h. The characterization study of the waste phosphors and the rare earth oxide products was performed by XRD, XRF, and SEM-EDS analysis to determine the phase and morphological features. Influences of the factors, such as roasting temperatures and time, the addition of ammonium chloride on the roasting of waste phosphors, as well as the pH and the amount of oxalates on the precipitation of Y and Eu, were investigated. The maximum grade (99.84% of mixed rare earth oxides and recovery rate (87.35% of Y and Eu were obtained at the optimized conditions.

  4. Effects of chlorine or chlorine dioxide during immersion chilling on recovery of bacteria from broiler carcasses and chiller water

    Science.gov (United States)

    A study was conducted to determine the microbiological impact of immersion chilling broiler carcasses with chlorine or chlorine dioxide. Eviscerated, pre-chill commercial broiler carcasses were cut into left and right halves along the keel bone, and each half was rinsed (HCR) in 100 mL of 0.1% pept...

  5. Change in genotoxicity of wastewater during chlorine dioxide and chlorine disinfections and the influence of ammonia nitrogen

    Institute of Scientific and Technical Information of China (English)

    WANG Lisha; HU Hongying; WANG Chao; Koichi Fujie

    2007-01-01

    The effects of chlorine dioxide and chlorine disinfections on the genotoxicity of different biologically treated sewage wastewater samples were studied by umu-test.The experiment results showed that when chlorine dioxide dosage was increased from 0 to 30 mg/L,the genotoxicity of wastewater first decreased rapidly and then tended to be stable,while when the chlorine dosage was increased from 0 to 30 mg/L,the genotoxicity of wastewater changed diversely for different samples.It was then found that ammonia nitrogen did not affect the change of genotoxicity during chlorine dioxide disinfection of wastewater,while it greatly affected the change of genotoxicity during chlorine disinfection of wastewater.When the concentration of ammonia nitrogen was low(<10-20mg/L),the genotoxicity of wastewater decreased after chlorine disinfection,and when the concentration of ammonia nitrogen was high(>10-20 mg/L),the genotoxicity of wastewater increased after chlorine disinfection.

  6. Postexposure aerosolized heparin reduces lung injury in chlorine-exposed mice

    OpenAIRE

    Zarogiannis, Sotirios G.; Wagener, Brant M.; Basappa, Susanna; Doran, Stephen; Rodriguez, Cilina A.; Jurkuvenaite, Asta; Pittet, Jean Francois; Matalon, Sadis

    2014-01-01

    Chlorine (Cl2) is a highly reactive oxidant gas that, when inhaled, may cause acute lung injury culminating in death from respiratory failure. In this study, we tested the hypothesis that exposure of mice to Cl2 causes intra-alveolar and systemic activation of the coagulation cascade that plays an important role in development of lung injury. C57Bl/6 mice were exposed to Cl2 (400 for 30 min or 600 ppm for 45 min) in environmental chambers and then returned to room air for 1 or 6 h. Native coa...

  7. Comparison of electrochemical method with ozonation, chlorination and monochloramination in drinking water disinfection

    Energy Technology Data Exchange (ETDEWEB)

    Li Hongna, E-mail: lihongna@gmail.com [Department of Environmental Engineering, Peking University, Key Laboratory of Water and Sediment Sciences, Ministry of Education, Beijing 100871 (China); Zhu Xiuping [Department of Environmental Engineering, Peking University, Key Laboratory of Water and Sediment Sciences, Ministry of Education, Beijing 100871 (China); Ni Jinren, E-mail: nijinren@iee.pku.edu.cn [Department of Environmental Engineering, Peking University, Key Laboratory of Water and Sediment Sciences, Ministry of Education, Beijing 100871 (China)

    2011-11-30

    Highlights: > Electrochemical, O{sub 3}, NaClO and NH{sub 2}Cl were compared at respective optimal condition. > Disinfection efficacy was similar for different bacteria in electrolysis. > Harsh Bacillus was inactivated more difficult in O{sub 3}, NaClO and NH{sub 2}Cl system. > Efficient disinfection of electrolysis was attributed to nonselectivity of {center_dot}OH. > Cell surface damage was more obvious in electrochemical process than the others. - Abstract: Electrochemical process in chloride-free electrolytes was proved to be powerful in disinfection due to the strong oxidants produced in the electrolysis and no formation of disinfection byproducts (DBPs). In this study, disinfection experiments were conducted by electrochemical treatment compared with ordinary and advanced methods (ozonation, chlorination and monochloramination), with Escherichia coli (E. coli) K-12, Staphylococcus aureus (S. aureus) A106, Bacillus subtilis (BST) and an isolated Bacillus as the representative microorganisms. Firstly, factor tests were performed on E. coli to obtain the optimal conditions of the four disinfection procedures. At their respective optimal condition, CT (concentration of disinfectant x contact time) value of a 4-log E. coli inactivation was 33.5, 1440, 1575, 1674 mg min L{sup -1} for electrochemical process, ozonation, chlorination and monochloramination, respectively. It was demonstrated that the disinfection availability was in the following order: electrochemical process > ozonation > chlorination > monochloramination, which could be attributed to the hydroxyl radical generated in the electrolysis, with strong oxidizing ability and non-selectivity compared with the other three disinfectants. Moreover, the disinfection efficacy of the four disinfection procedures was compared for four different bacteria. It was found that the disinfection efficacy was similar for the selected four bacteria in electrochemical process, while in the other three treatments

  8. Quantitative structure–activity relationships (QSARs) for the transformation of organic micropollutants during oxidative water treatment

    OpenAIRE

    Lee, Yunho; VON GUNTEN, Urs

    2012-01-01

    Various oxidants such as chlorine, chlorine dioxide, ferrateVI, ozone, and hydroxyl radicals can be applied for eliminating organic micropollutant by oxidative transformation during water treatment in systems such as drinking water, wastewater, and water reuse. Over the last decades, many second-order rate constants (k) have been determined for the reaction of these oxidants with model compounds and micropollutants. Good correlations (quantitative structure–activity relationships or QSARs) ar...

  9. Synergetic Inactivation of Microorganisms in Drinking Water by Short-term Free Chlorination and Subsequent Monochloramination

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    To introduce synergetic inactivation of microorganisms in drinking water by short-term free chlorination for less than 15 minutes followed by monochloramination. Methods Indicator microorganisms such as Escherichia coli,Staphylococcus aureus, Candida albicans, and spores of Bacillus subtilis were used to assess the efficiency of sequential chlorination and free chlorination. Results The sequential chlorination was more efficient in inactivating these microorganisms than free chlorination, indicating that synergy was provided by free chlorine and monochloramine. Ammonia addition time, temperature and pH had influences on this synergy. Conclusion The possible mechanism of this synergy might involve three aspects: free chlorine causing sublethal injury to microorganisms and monochloramine further inactivating them; different ability of free chlorine and monochloramine to penetrate and inactivate microorganism congeries; and higher concentration of residual chlorine in sequential chlorination than in free chlorination.

  10. Appraisal of chlorine contact tank modelling practices.

    Science.gov (United States)

    Rauen, William B; Angeloudis, Athanasios; Falconer, Roger A

    2012-11-15

    With new water directives imposing strict regulations to reduce the footprint of treatment operations and contaminant levels, a performance review of water treatment facilities, including Chlorine Contact Tanks (CCTs) is required. This paper includes a critical appraisal of the international literature on CCT modelling practices to date, aiming to assist the identification of areas requiring further development, in particular, relating to the computational modelling capability and availability of tools to assist hydraulic design and optimisation studies of CCTs. It notes that the hydraulic optimisation practice of poorly designed tanks commenced with experimental studies undertaken in the 1960s and 1970s, which involved mainly two types of studies, namely in situ tracer tests and laboratory physical modelling. The former has traditionally been conducted to diagnose the hydraulic performance of existing CCTs, typically based on results such as Residence Time Distribution (RTD) curves and values of the Hydraulic Efficiency Indicators (HEIs). The latter has been useful in trial and error testing of the impact of certain design modifications on those results, with suggestions for later improvements of the field scale unit. In the 1980s mathematical and numerical modelling studies started to be used to assist CCT investigations, offering a greater level of detail in a more cost-effective manner than equivalent experimentally based investigations. With the growth of computing power and the popularisation of computational models, the 1990s saw the development and application of Computational Fluid Dynamics (CFD) tools to simulate the hydraulic performance of CCTs, sometimes independently of experimentation, other than by using available data to calibrate and validate modelling predictions. This has led to the current scenario of CFD models being invaluable assistive tools in optimisation studies of CCTs, with the experimentation practice continuing to allow for specific

  11. Chlorine Isotopes: As a Possible Tracer of Fluid/Bio-Activities on Mars and a Progress Report on Chlorine Isotope Analysis by TIMs

    Science.gov (United States)

    Nakamura, N.; Nyquist, L.E.; Reese, Y.; Shih, C-Y.; Numata, M.; Fujitani, T.; Okano, O.

    2009-01-01

    Significantly large mass fractionations between chlorine isotopes (Cl-35, Cl-37) have been reported for terrestrial materials including both geological samples and laboratory materials. Also, the chlorine isotopic composition can be used as a tracer for early solar system processes. Moreover, chlorine is ubiquitous on the Martian surface. Typical chlorine abundances in Gusev soils are approx.0.5 %. The global surface average chlorine abundance also is approx.0.5 %. Striking variations among outcrop rocks at Meridiani were reported with some chlorine abundances as high as approx.2%. Characterizing conditions under which chlorine isotopic fractionation may occur is clearly of interest to planetary science. Thus, we have initiated development of a chlorine isotopic analysis technique using TIMS at NASA-JSC. We present here a progress report on the current status of development at JSC and discuss the possible application of chlorine isotopic analysis to Martian meteorites in a search for fluid- and possibly biological activity on Mars.

  12. Anaerobic Degradation of Chlorinated Hydrocarbons in Groundwater Aquifers or "Chlorinated Hydrocarbon Degradation"

    OpenAIRE

    Nielsen, R. Brent; Jay D Keasling

    1997-01-01

    Groundwater contamination by chlorinated hydrocarbons, such as tetrachloroethene (PCE) or trichloroethene (TCE), is a major concern throughout the United States. A developing strategy for the remediation of PCE and TCE contaminated aquifers is anaerobic biodegradation. From a TCE contaminated groundwater site, microorganisms were enriched with the ability to anaerobically convert PCE and TCE completely to ethene. Kinetic studies performed with this culture showed that degradation of PCE, TCE...

  13. Thermal and under irradiation diffusion of chlorine in uranium dioxide

    International Nuclear Information System (INIS)

    This work concerns the study of the thermal and radiation enhanced diffusion of 36Cl in uranium dioxide. We simulated the presence of 36Cl by implanting a quantity of 37Cl comparable to the impurity content of chlorine in UO2. In order to evaluate the diffusion properties of chlorine in the fuel and in particular to assess the influence of the irradiation defects, we performed two kinds of experiments: - the influence of the temperature was studied by carrying out thermal annealings in the temperature range 900 - 1300 C; we showed that implanted chlorine was mobile from temperatures as low as 1000 C and determined a thermal diffusion coefficient D1000 C around 10-16 cm2s-1 - the influence of the irradiation by fission products were studied by irradiating the samples with 127I (energy of 63.5 MeV). We could determine that the diffusion of the implanted chlorine under irradiation and in the range of temperature 30 - 250 C was not purely athermal. We calculated a diffusion coefficient under irradiation D250 C of about 0-14 cm2.s-1. We showed the importance of the implantation and irradiation defects as preferential paths for a fast chlorine transport. We carried out ab initio calculations showing that chlorine is preferentially located in a substitutional site. This is in favour of a Frank-Turnbull diffusion mechanism or a vacancy/chlorine. (author)

  14. Does chlorination of seawater reverse osmosis membranes control biofouling?

    Science.gov (United States)

    Khan, Muhammad Tariq; Hong, Pei-Ying; Nada, Nabil; Croue, Jean Philippe

    2015-07-01

    Biofouling is the major problem of reverse osmosis (RO) membranes used for desalting seawater (SW). The use of chlorine is a conventional and common practice to control/prevent biofouling. Unlike polyamide RO membranes, cellulose triacetate (CTA) RO membranes display a high chlorine tolerance. Due to this characteristic, CTA membranes are used in most of the RO plants located in the Middle East region where the elevated seawater temperature and water quality promote the risk of membrane biofouling. However, there is no detailed study on the investigation/characterization of CTA-RO membrane fouling. In this investigation, the fouling profile of a full-scale SWRO desalination plant operating with not only continuous chlorination of raw seawater but also intermittent chlorination of CTA-RO membranes was studied. Detailed water quality and membrane fouling analyses were conducted. Profiles of microbiological, inorganic, and organic constituents of analysed fouling layers were extensively discussed. Our results clearly identified biofilm development on these membranes. The incapability of chlorination on preventing biofilm formation on SWRO membranes could be assigned to its failure in effectively reaching throughout the different regions of the permeators. This failure could have occurred due to three main factors: plugging of membrane fibers, chlorine consumption by organics accumulated on the front side fibers, or chlorine adaptation of certain bacterial populations. PMID:25917390

  15. Does Chlorination of Seawater Reverse Osmosis Membranes Control Biofouling?

    KAUST Repository

    Khan, Muhammad Tariq

    2015-04-01

    Biofouling is the major problem of reverse osmosis (RO) membranes used for desalting seawater (SW). The use of chlorine is a conventional and common practice to control/prevent biofouling. Unlike polyamide RO membranes, cellulose triacetate (CTA) RO membranes display a high chlorine tolerance. Due to this characteristic, CTA membranes are used in most of the RO plants located in the Middle East region where the elevated seawater temperature and water quality promote the risk of membrane biofouling. However, there is no detailed study on the investigation/characterization of CTA-RO membrane fouling. In this investigation, the fouling profile of a full–scale SWRO desalination plant operating with not only continuous chlorination of raw seawater but also intermittent chlorination of CTA-RO membranes was studied. Detailed water quality and membrane fouling analyses were conducted. Profiles of microbiological, inorganic, and organic constituents of analysed fouling layers were extensively discussed. Our results clearly identified biofilm development on these membranes. The incapability of chlorination on preventing biofilm formation on SWRO membranes could be assigned to its failure in effectively reaching throughout the different regions of the permeators. This failure could have occurred due to three main factors: plugging of membrane fibers, chlorine consumption by organics accumulated on the front side fibers, or chlorine adaptation of certain bacterial populations.

  16. Does chlorination of seawater reverse osmosis membranes control biofouling?

    Science.gov (United States)

    Khan, Muhammad Tariq; Hong, Pei-Ying; Nada, Nabil; Croue, Jean Philippe

    2015-07-01

    Biofouling is the major problem of reverse osmosis (RO) membranes used for desalting seawater (SW). The use of chlorine is a conventional and common practice to control/prevent biofouling. Unlike polyamide RO membranes, cellulose triacetate (CTA) RO membranes display a high chlorine tolerance. Due to this characteristic, CTA membranes are used in most of the RO plants located in the Middle East region where the elevated seawater temperature and water quality promote the risk of membrane biofouling. However, there is no detailed study on the investigation/characterization of CTA-RO membrane fouling. In this investigation, the fouling profile of a full-scale SWRO desalination plant operating with not only continuous chlorination of raw seawater but also intermittent chlorination of CTA-RO membranes was studied. Detailed water quality and membrane fouling analyses were conducted. Profiles of microbiological, inorganic, and organic constituents of analysed fouling layers were extensively discussed. Our results clearly identified biofilm development on these membranes. The incapability of chlorination on preventing biofilm formation on SWRO membranes could be assigned to its failure in effectively reaching throughout the different regions of the permeators. This failure could have occurred due to three main factors: plugging of membrane fibers, chlorine consumption by organics accumulated on the front side fibers, or chlorine adaptation of certain bacterial populations.

  17. Behavior and stability of adenosine triphosphate (ATP) during chlorine disinfection.

    Science.gov (United States)

    Nescerecka, Alina; Juhna, Talis; Hammes, Frederik

    2016-09-15

    Adenosine triphosphate (ATP) analysis is a cultivation-independent alternative method for the determination of bacterial viability in both chlorinated and non-chlorinated water. Here we investigated the behavior and stability of ATP during chlorination in detail. Different sodium hypochlorite doses (0-22.4 mg-Cl2 L(-1); 5 min exposure) were applied to an Escherichia coli pure culture suspended in filtered river water. We observed decreasing intracellular ATP with increasing chlorine concentrations, but extracellular ATP concentrations only increased when the chlorine dose exceeded 0.35 mg L(-1). The release of ATP from chlorine-damaged bacteria coincided with severe membrane damage detected with flow cytometry (FCM). The stability of extracellular ATP was subsequently studied in different water matrixes, and we found that extracellular ATP was stable in sterile deionized water and also in chlorinated water until extremely high chlorine doses (≤11.2 mg-Cl2 L(-1); 5 min exposure). In contrast, ATP decreased relatively slowly (k = 0.145 h(-1)) in 0.1 μm filtered river water, presumably due to degradation by either extracellular enzymes or the fraction of bacteria that were able to pass through the filter. Extracellular ATP decreased considerably faster (k = 0.368 h(-1)) during batch growth of a river water bacterial community. A series of growth potential tests showed that extracellular ATP molecules were utilized as a phosphorus source during bacteria proliferation. From the combined data we conclude that ATP released from bacteria at high chlorine doses could promote bacteria regrowth, contributing to biological instability in drinking water distribution systems. PMID:27295623

  18. Behavior and stability of adenosine triphosphate (ATP) during chlorine disinfection.

    Science.gov (United States)

    Nescerecka, Alina; Juhna, Talis; Hammes, Frederik

    2016-09-15

    Adenosine triphosphate (ATP) analysis is a cultivation-independent alternative method for the determination of bacterial viability in both chlorinated and non-chlorinated water. Here we investigated the behavior and stability of ATP during chlorination in detail. Different sodium hypochlorite doses (0-22.4 mg-Cl2 L(-1); 5 min exposure) were applied to an Escherichia coli pure culture suspended in filtered river water. We observed decreasing intracellular ATP with increasing chlorine concentrations, but extracellular ATP concentrations only increased when the chlorine dose exceeded 0.35 mg L(-1). The release of ATP from chlorine-damaged bacteria coincided with severe membrane damage detected with flow cytometry (FCM). The stability of extracellular ATP was subsequently studied in different water matrixes, and we found that extracellular ATP was stable in sterile deionized water and also in chlorinated water until extremely high chlorine doses (≤11.2 mg-Cl2 L(-1); 5 min exposure). In contrast, ATP decreased relatively slowly (k = 0.145 h(-1)) in 0.1 μm filtered river water, presumably due to degradation by either extracellular enzymes or the fraction of bacteria that were able to pass through the filter. Extracellular ATP decreased considerably faster (k = 0.368 h(-1)) during batch growth of a river water bacterial community. A series of growth potential tests showed that extracellular ATP molecules were utilized as a phosphorus source during bacteria proliferation. From the combined data we conclude that ATP released from bacteria at high chlorine doses could promote bacteria regrowth, contributing to biological instability in drinking water distribution systems.

  19. Stability and effectiveness of chlorine disinfectants in water distribution systems.

    OpenAIRE

    Olivieri, V P; Snead, M C; Krusé, C W; Kawata, K.

    1986-01-01

    A test system for water distribution was used to evaluate the stability and effectiveness of three residual disinfectants--free chlorine, combined chlorine, and chlorine dioxide--when challenged with a sewage contaminant. The test distribution system consisted of the street main and internal plumbing for two barracks at Fort George G. Meade, MD. To the existing pipe network, 152 m (500 ft) of 13-mm (0.5 in.) copper pipe were added for sampling, and 60 m (200 ft) of 2.54-cm (1.0 in.) plastic p...

  20. INFRARED VIBRATIONAL SPECTRA OF CHLORINATED AND HYDROGENATED AMORPHOUS SILICON

    OpenAIRE

    Kalem, S; Chevallier, J.; Al Dallal, S.; Bourneix, J.

    1981-01-01

    The infrared spectra of chlorinated and hydrogenated amorphous silicon have been measured. In addition to the hydrogen induced bands at 2110, 1990, 885, 840 and 640 cm-1, we observe two new modes at 545 cm-1 (Si-Cl stretching) and 500 cm-1 ( Si TO modes induced by chlorine). Observation of the 545 cm-1 band proves that chlorine acts as a dangling bond terminator. Upon annealing, some of the Si-Cl groups transform into SiCl4 molecules (SiCl4 stretching at 615 cm-1). A good agreement is found b...

  1. THM reduction on water distribution network with chlorine dioxide as disinfectant; Reduccion de THM en red de distribucion utilizando dioxido de cloro como desinfectante

    Energy Technology Data Exchange (ETDEWEB)

    Ventura, G.; Gorriz, D.; Pascual, E.; Romero, M.

    2009-07-01

    A disinfectant change on water distribution network, by chlorine dioxide in that case, avoids THM formation. In the other hand it creates big doubts about utilization and analytical determination of another oxidant different to chlorine. Just a need to comply the current legislation points us to make a change as the one mentioned above and carried out in DWTP Rio Verde, being managed by Acosol, where the THM formation is been reduced to 80%, according to the new limit of 100{mu}g/l, along the 200 km of the supply network. (Author) 13 refs.

  2. A contribution of research by chlorination from nickel silicate and nickel ferrite in the presence of calcium chloride and coke with possibilities of their intensification

    OpenAIRE

    Krstev, Boris

    1988-01-01

    The previous investigations in the field of the metal compounds chlorination of the refractory nickel minerals: garnierite and nontronite, by the chlorine, Cl2, HCl, NaCl or CaCl2, were determined directions, confirming the perspective of the mentioned process for the treatment of the low grade and complex minerals-laterites. The existing combined methods for enriching of the oxide-silicate nickel ores are these through which by heating the ore with coke and CaCl2 at high temperature reduced...

  3. Use of chlorination, ozonization and GAC adsorption to eliminate triazine pesticides in water supplies; Eliminacion de plaguicidas en aguas de abastecimiento mediante cloracion, ozonizacion y adsorcion con GAC

    Energy Technology Data Exchange (ETDEWEB)

    Ormad Melero, M. P.; Garcia Castillo, F. J.; Munarriz Cid, B.

    2009-07-01

    This study is focused on the research made between Facsa and Universidad de Zaragoza (Spain) related to the oxidation techniques application by chlorination and ozonization, and their combination with granular activated carbon (GAC) adsorption of mineral origin, in order to control triazine pesticides in water supplies. Experiments are carried out is a pilot plant. Although the chlorination or ozonization can partially degrade pesticides under study (atrazine, simazine, terbutilazine and bromacil), their passing through an adsorption column with GAC mineral, achieves their total removal when their initial concentrations are about 500 ng/l. These concentrations are obtained by fortification of studied sample. (Author) 9 refs.

  4. Removal of carbamazepine in aqueous solutions through solar photolysis of free available chlorine.

    Science.gov (United States)

    Yang, Bin; Kookana, Rai S; Williams, Mike; Du, Jun; Doan, Hai; Kumar, Anupama

    2016-09-01

    Removal of a persistent antiepileptic drug carbamazepine (CBZ) in aqueous solutions was investigated by using solar photolysis combined with free available chlorine (FAC). The combination of chlorination with simulated or natural sunlight markedly enhanced removal of CBZ in 10 mM phosphate buffer solution (pH 7.0) and river water (pH 7.0) compared with sunlight or FAC alone. Further analysis indicated that the observed enhancements in CBZ removal can be attributed to the in situ hydroxyl radical (HO) and ozone (O3) production during FAC photolysis. During 70 min simulated sunlight photolysis combined with FAC treatment, HO reaction contributed to 35.8% removal of CBZ and O3 reaction contributed to 40.6% removal, while only 5.3% of CBZ was removed by HOCl reaction. The oxidation products of CBZ, epoxide CBZ, 10,11-dihydro-10,11-dihydroxy CBZ, 1-(2-benzaldehyde)-4-hydro-(1H,3H)-quinazoline-2-one (BQM), 1-(2-benzaldehyde)-(1H,3H)-quinazoline-2,4-dione (BQD) and 4-aldehyde-9-acridone, were mainly formed from the HO and O3 attack at the double bond on the central heterocyclic ring of CBZ. Formation of these oxidation products did not cause any increase or decrease in toxicity to microbial species tested through Microbial Assay for Toxicity Risk Assessment (MARA). The initial FAC concentration and pH had a major influence on the removal process of CBZ during FAC photolysis, while temperature had a minor effect only. The combination of chlorination with natural sunlight could provide an effective approach for removal of CBZ and other contaminants during water treatment. PMID:27232985

  5. Effect of the temperature and the chlorine pressure, over the aluminium chlorides obtained by direct chlorination of the 6061 alloy

    International Nuclear Information System (INIS)

    The aluminium chloride is synthesized by direct chlorination of aluminium, in agreement with the following reaction: Al(s) + 3/2 Cl2 AlCl3 (s,g).The present work focuses on the preparation of aluminium chlorides by two methods: (a) Chlorination of 6061 aluminium alloy with gaseous chlorine in sealed containers, filled with different pressures of gas, from 0.8 to 74 Kpa and in the range of temperature between 2000 and 5000C.(b) Chlorination of the same alloy in chlorine flow between 1500 and 4000C.In the sealed systems, the hexahydrated aluminium trichloride predominated over the anhydrous form. For pressures lower than 14 Kpa and temperatures under 2500C, the chloride didn't appear.The residues were rich in aluminium, chlorine and magnesium.In the other systems, the anhydrous chloride was found in the areas of the reactor of temperatures above 1000C, for all the thermal treatments. The waste was composed by CrCl3 and AlCl3.6H2O.The influence of the chlorine pressures and the heating temperature over the characteristics of the product, was studied.The characterization techniques were x-ray diffraction and energy dispersive spectroscopy, and the evolution of the structure was followed by scanning electron microscopy

  6. RESEARCH ON MATHEMATICAL SIMULATION OF RESIDUAL CHLORINE DECAY AND OPTIMIZATION OF CHLORINATION ALLOCATION OF URBAN WATER DISTRIBUTION SYSTEM

    Institute of Scientific and Technical Information of China (English)

    TIAN Yi-mei; CHI Hai-yan; LI Hong; SHAN Jin-lin; ZHAI Chun-nian

    2005-01-01

    The concentration of Residual Chlorine (RC) frequently violates the standard in situations of urban water distribution system with large water supply area and long time of distribution.If chlorine dosage increases within water treatment plant, although RC in distribution system could meet water quality standard, Disinfection By-Products (DBPs) such as hydrocarbon halide rises.In the paper, a mathematical model of chlorine allocation optimization was presented based on reaction kinetics mechanism and optimization theory to solve the problem.The model includes the objective function of minimizing annual operation cost and constraints of RC standard and rational chlorination station distribution, and solving by 0-1 Integer Programming (IP).The model had been applied to a real water distribution system.The simulation results of the model showed that adding chlorine in water distribution system remarkably improved water quality and reduced the operation cost by 49.3% per year less than chlorine dosed only in water treatment plant to meet RC standard.The results prove adding chlorine in water distribution system based on the model can bring both technological and economic advancement.

  7. Reactivity of lignin and problems of its oxidative destruction with peroxy reagents

    International Nuclear Information System (INIS)

    Published data on reactivity and oxidation of lignin and model compounds with hydrogen peroxide, ozone and chlorine dioxide as well as on oxidative destruction of the sulfate pulp lignin with various reagents during bleaching are systematised and generalised. Concepts of lignin activation towards its selective oxidation and kinetic features of sulfate pulp oxidative delignification are considered. The bibliography includes 157 references.

  8. Behavior of Zn and Fe Content in Electric Arc Furnace Dust as Submitted to Chlorination Methods

    Science.gov (United States)

    Santos, Felipe; Brocchi, Eduardo; Araújo, Victor; Souza, Rodrigo

    2015-08-01

    This work covers initially a general thermodynamics assessment regarding the zinc ferrite (ZnFe2O4) behavior toward direct and reducing chlorination. Then, the use of alternative chlorination agents were also theoretically appreciated, before a set of experiments has been carried out with industrial residue (electric arc furnace dust). Besides identifying zinc ferrite (95.4 pct), the XRD analysis indicated the presence of ZnO (4.6 pct). Therefore, the main objective of the present work is related to a theoretical (thermodynamics) and experimental (kinetics) evaluation of the mentioned residue chemical behavior as submitted to chlorination methods. Several characterization methods were used, such as X-ray diffraction, scanning electron microscopy, X-ray fluorescence, mass spectroscopy (ICP-MS), and energy-dispersive X-ray spectroscopy (EDS). It was observed that zinc was present, mostly, in the form of zinc ferrite (franklinite). The thermodynamics study revealed that Zn has a more susceptible behavior regarding the oxides conversion into chlorides. However, this tendency is not necessarily associated with a selective reaction, as showed for the chlorination in the presence of carbon, as both iron and zinc chlorides formation is feasible. The experimental results have indicated that some reaction systems can be further studied in order to identify operational conditions that enable selective formations. So, it was observed that for the calcium chloride reaction conducted at 1273 K (1000 °C) for 30 minutes, the iron content in the residue slightly increases (with 15 pct removal), whereas the zinc content decreases from 20 to 12 pct (53 pct removal), suggesting complementary studies where this possible selectivity could be even more determinant. Such results have also indicated that the direct action of chlorine at 1073 K (800 °C) allowed complete removal of zinc, followed by conversion in the order of 40 pct in iron. Therefore, a complementary investigation over

  9. Assessing the Impact of Chlorinated-Solvent Sites on Metropolitan Groundwater Resources

    OpenAIRE

    Brusseau, Mark L.; Narter, Matthew

    2013-01-01

    Chlorinated-solvent compounds are among the most common groundwater contaminants in the U.S.A. The majority of the many sites contaminated by chlorinated-solvent compounds are located in metropolitan areas, and most such areas have one or more chlorinated-solvent contaminated sites. Thus, contamination of groundwater by chlorinated-solvent compounds may pose a potential risk to the sustainability of potable water supplies for many metropolitan areas. The impact of chlorinated-solvent sites on...

  10. MULTISPECTRAL IDENTIFICATION OF CHLORINE DIOXIDE BYPRODUCTS IN DRINKING WATER

    Science.gov (United States)

    This paper discusses the identification of organic disinfectant byproducts (DNPS) at a pilot plant in Evansville, IN, that uses chlorine dioxide as a primary disinfectant. nconventional multispectral identification techniques (gas chromatography combined with high- and low-resolu...

  11. MICROEMULSION OF MIXED CHLORINATED SOLVENTS USING FOOD GRADE (EDIBLE) SURFACTANTS

    Science.gov (United States)

    Ground water contamination frequently consists of mixed chlorinated solvents [e.g., tetrachloroethylene (PCE), trichloroethylene (TCE), and trans-1,2- dichloroethylene (DCE)]. In this research, mixtures of the food grade (edible) surfactants bis(2-ethylhexyl) sodium sulfosuccinat...

  12. Modeling of residual chlorine in water distribution system

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    Water quality within water distribution system may vary with both location and time. Water quality models are used to predict the spatial and temporal variation of water quality throughout water system. A model of residual chlorine decay in water pipe has been developed,given the consumption of chlorine in reactions with chemicals in bulk water, bio-films on pipe wall, in corrosion process, and the mass transport of chlorine from bulk water to pipe wall. Analytical methods of the flow path from water sources to the observed point and the water age of every observed node were proposed. Model is used to predict the decay of residual chlorine in an actual distribution system. Good agreement between calculated and measured values was obtained.

  13. In situ bioremediation of chlorinated solvent with natural gas

    International Nuclear Information System (INIS)

    A bioremediation system for the removal of chlorinated solvents from ground water and sediments is described. The system involves the the in-situ injection of natural gas (as a microbial nutrient) through an innovative configuration of horizontal wells

  14. The chlorination kinetics of zirconium dioxide mixed with carbon black

    International Nuclear Information System (INIS)

    In this research, the effects of chlorine gas at different chlorine partial pressures and carbon concentrations on the carbochlorination of zirconia were studied. It was found that in briquettes containing 18.7 %wt carbon, in a chlorine partial pressure range of 0.25-0.75 atm and for a reacted fraction of less than 0.7, the chemical reaction model was dominant for the carbochlorination process of zirconia. The order of reaction into chlorine gas (n) in this situation was 0.57. Moreover, the best weight ratio of carbon to zirconia was 40/60. In this case, the activation energy of the reaction was 209.9 kJ mol-1 in a temperature range of 1023-1223 K, and the dominant model was the chemical reaction model.

  15. Effect of Chlorine Dioxide Gas on Polymeric Packaging Materials

    Science.gov (United States)

    Permeability, solubility and diffusion coefficients of chlorine dioxide for high-density polyethylene (HDPE), low-density polyethylene (LDPE), linear low-density polyethylene (LLDPE), polyvinyl chloride (PVC), polystyrene (PS), polyethylene terephthalate (PET), nylon, and multilayer of ethylene viny...

  16. Bioremediation of chlorinated ethenes in aquifer thermal energy storage

    NARCIS (Netherlands)

    Ni, Z.

    2015-01-01

      Subjects: bioremediation; biodegradation; environmental biotechnology, subsurface and groundwater contamination; biological processes; geochemistry; microbiology The combination of enhanced natural attenuation (ENA) of chlorinated volatile organic compounds (CVOCs) and aquife

  17. Determination of chlorine in graphite by combustion-ion chromatography

    Energy Technology Data Exchange (ETDEWEB)

    Chen Lianzhong [Academia Sinica, Beijing, BJ (China). Inst. of Atomic Energy; Watanabe, Kazuo; Itoh, Mitsuo

    1995-09-01

    A combustion/ion chromatographic method has been studied for the sensitive determination of chlorine in graphite. A graphite sample was burnt at 900degC in a silica reaction tube at an oxygen flow rate of 200 ml/min. Chlorine evolved was absorbed in 20 ml of a 0.1 mM sodium carbonate solution. The solution was evaporated to dryness. The residue was dissolved with a small volume of water. Chlorine in the solution was determined using ion chromatography. The method was applied to JAERI graphite certified reference materials and practical graphite materials. The detection limit was about 0.8 {mu}gCl/g for a 2.0 g sample. The precision was about 2.5% (relative standard deviation) for samples with chlorine content of 70 {mu}g/g level. The method is also usable for coal samples. (author).

  18. Release of Chlorine and Sulfur during Biomass Torrefaction and Pyrolysis

    DEFF Research Database (Denmark)

    Saleh, Suriyati Binti; Flensborg, Julie Pauline; Shoulaifar, Tooran Khazraie;

    2014-01-01

    The release of chlorine (Cl) and sulfur (S) during biomass torrefaction and pyrolysis has been investigated via experiments in two laboratory-scale reactors: a rotating reactor and a fixed bed reactor. Six biomasses with different chemical compositions covering a wide range of ash content and ash......-forming elements were torrefied/pyrolyzed in the temperature range of 150-500 degrees C. The relative release of chlorine and sulfur was calculated based on mass balance and analysis of the biomass before and after torrefaction. In selected cases, measurement of methyl chloride (CH3Cl) in the gas from straw...... torrefaction has furthermore been conducted. The release of chlorine from straw was first observed at 250 degrees C and peaked with about 60-70% at 350 degrees C. Analysis of the released gas showed that most of the chlorine was released as methyl chloride. Increasing the straw content in the reactor resulted...

  19. ANAEROBIC AND AEROBIC TREATMENT OF CHLORINATED ALIPHATIC COMPOUNDS

    Science.gov (United States)

    Biological degradation of 12 chlorinated aliphatic compounds (CACs) was assessed in bench-top reactors and in serum bottle tests. Three continuously mixed daily batch-fed reactor systems were evaluated: anaerobic, aerobic, and sequential-anaerobic-aerobic (sequential). Glucose,...

  20. Complete Non-Radioactive Operability Tests for Cladding Hull Chlorination

    Energy Technology Data Exchange (ETDEWEB)

    Collins, Emory D [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Johnson, Jared A. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Hylton, Tom D. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Brunson, Ronald Ray [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Hunt, Rodney Dale [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); DelCul, Guillermo Daniel [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Bradley, Eric Craig [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Spencer, Barry B. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

    2016-04-01

    Non-radioactive operability tests were made to test the metal chlorination reactor and condenser and their accessories using batch chlorinations of non-radioactive cladding samples and to identify optimum operating practices and components that need further modifications prior to installation of the equipment into the hot cell for tests on actual used nuclear fuel (UNF) cladding. The operability tests included (1) modifications to provide the desired heating and reactor temperature profile; and (2) three batch chlorination tests using, respectively, 100, 250, and 500 g of cladding. During the batch chlorinations, metal corrosion of the equipment was assessed, pressurization of the gas inlet was examined and the best method for maintaining solid salt product transfer through the condenser was determined. Also, additional accessing equipment for collection of residual ash and positioning of the unit within the hot cell were identified, designed, and are being fabricated.

  1. Determination of chlorine in graphite by combustion-ion chromatography

    International Nuclear Information System (INIS)

    A combustion/ion chromatographic method has been studied for the sensitive determination of chlorine in graphite. A graphite sample was burnt at 900degC in a silica reaction tube at an oxygen flow rate of 200 ml/min. Chlorine evolved was absorbed in 20 ml of a 0.1 mM sodium carbonate solution. The solution was evaporated to dryness. The residue was dissolved with a small volume of water. Chlorine in the solution was determined using ion chromatography. The method was applied to JAERI graphite certified reference materials and practical graphite materials. The detection limit was about 0.8 μgCl/g for a 2.0 g sample. The precision was about 2.5% (relative standard deviation) for samples with chlorine content of 70 μg/g level. The method is also usable for coal samples. (author)

  2. MULTISPECTRAL IDENTIFICATION OF CHLORINE DIOXIDE DISINFECTION BYPRODUCTS IN DRINKING WATER

    Science.gov (United States)

    This paper discusses the identification of organic disinfection byproducts (DBPs) at a pilot plant in Evansville, IN, which uses chlorine dioxide as a primary disinfectant. Unconventional multispectral identification techniques (gas chromatography combined with high- and low reso...

  3. CHLORINE INACTIVATION OF CATEGORY "A" BIO-TERRORISM AGENTS

    Science.gov (United States)

    This poster presents information on the inactivation of select bioterrorist agents. Information will be presented on chlorine disinfection of vegetative cells of Brucella suis, Brucella melitensis, Burkholderia mallei, Burkholderia pseudomallei, Francisella tularensis and endos...

  4. Kinetics of Chlorine Decay in Water Distribution Systems

    Institute of Scientific and Technical Information of China (English)

    周建华; 薛罡; 赵洪宾; 汪永辉; 郭美芳

    2004-01-01

    A combined first and second-order model, which includes bulk decay and wall decay, was developed to describe chlorine decay in water distribution systems. In the model the bulk decay has complex relationships with total organic carbon (TOC), the initial chlorine concentration and the temperature. Except for the initial stages they can be simplified into a linear increase with TOC, a linear decrease with initial chlorine concentration and an exponential relationship with the temperature. The model also explains why chlorine decays rapidly in the initial stages. The parameters of model are determined by deriving the best fitness with experimental data. And the accuracy of model has been verified by using the experimental data and the monitoring data in a distribution system.

  5. SCENARIOS EVALUATION TOOL FOR CHLORINATED SOLVENT MNA

    Energy Technology Data Exchange (ETDEWEB)

    Vangelas, K; Brian02 Looney, B; Michael J. Truex; Charles J. Newell

    2006-08-16

    Over the past three decades, much progress has been made in the remediation of chlorinated solvents from the subsurface. Yet these pervasive contaminants continue to present a significant challenge to the U.S. Department of Energy (DOE), other federal agencies, and other public and private organizations. The physical and chemical properties of chlorinated solvents make it difficult to rapidly reach the low concentrations typically set as regulatory limits. These technical challenges often result in high costs and long remediation time frames. In 2003, the DOE through the Office of Environmental Management funded a science-based technical project that uses the U.S. Environmental Protection Agency's technical protocol (EPA, 1998) and directives (EPA, 1999) on Monitored Natural Attenuation (MNA) as the foundation on which to introduce supporting concepts and new scientific developments that will support remediation of chlorinated solvents based on natural attenuation processes. This project supports the direction in which many site owners want to move to complete the remediation of their site(s), that being to complete the active treatment portion of the remedial effort and transition into MNA. The overarching objective of the effort was to examine environmental remedies that are based on natural processes--remedies such as Monitored Natural Attenuation (MNA) or Enhanced Attenuation (EA). The research program did identify several specific opportunities for advances based on: (1) mass balance as the central framework for attenuation based remedies, (2) scientific advancements and achievements during the past ten years, (3) regulatory and policy development and real-world experience using MNA, and (4) exploration of various ideas for integrating attenuation remedies into a systematic set of ''combined remedies'' for contaminated sites. These opportunities are summarized herein and are addressed in more detail in referenced project documents and

  6. Study on application of chlorine dioxide in oilfield sewage treatment%二氧化氯在油田污水处理中的应用研究

    Institute of Scientific and Technical Information of China (English)

    叶兴平

    2012-01-01

    Due to its good oxidative bactericidal action, chlorine dioxide could effectively remove the reduction chemicals such as iron and sulfur, which led to corrosion and scaling, and the bacteria in the oilfield sewage. Practical use of chlorine dioxide in oilfield water injection enhanced oil recovery was summarized and it showed that chlorine dioxide could have a well application prospect in this field.%由于二氧化氯具有良好的氧化杀菌作用,可以有效地去除油田污水中铁、硫等具有腐蚀性和结垢性的还原性物质,以及杀灭油田污水中的细菌微生物.考察了它在油田注水采油中应用情况,展示了它在油田注水采油中应用前景.

  7. Survival of Campylobacter jejuni in biofilms after chlorine treatment

    Directory of Open Access Journals (Sweden)

    Kunyaboon, S

    2006-09-01

    Full Text Available Survival of C. jejuni in biofilms isolated from two chicken houses in Thailand (FBRL-C04, FBRLB05 and FBRL-B06 after chlorine treatment was studied. Biofilm cultures were grown on stainless steel surface in 50% trypticase soy broth for 3 days, subsequently C. jejuni cells were allowed to attach to these biofilms for 4 h at 25ºC. Sodium hypochlorite was used to prepare sanitizing solution with active chlorine of 15 ppm and 25 ppm. Stainless steel coupons containing C. jejuni with and without biofilms were treated with chlorine for 30 sec and neutralized with 0.05% sodium thiosulfate. At both concentrations, C. jejuni were inactivated to lower than 1 log10CFU/cm2 when initial attachment load was approximately 4 log10CFU/cm2. However, C. jejuni in all samples treated with 15 ppm active chlorine were recovered in enrichment media. When treated with the higher concentration of chlorine, 25 ppm, C. jejuni in biofilm of FBRL-C04 (5/9, FBRL-B06 (1/9 and biofilm-free surface (1/9 could also be recovered. This indicates that chlorine treatment at 15 and 25 ppm could not completely inactivate C. jejuni attached to biofilms and biofilm-free surfaces. Biofilm of FBRL-C04 enhanced the survival of C. jejuni after chlorine treatment at 25 ppm although biofilm initial attachment as determined by plate count method was similar to that of other biofilms. Attachment load of viable biofilm cells may not contribute to enhanced survival of C. jejuni in chlorine treatment.

  8. Bromoform production in tropical open-ocean waters: OTEC chlorination

    Energy Technology Data Exchange (ETDEWEB)

    Hartwig, E.O.; Valentine, R.

    1981-09-01

    The bromoform, and other volatile organics produced while chlorinating both the evaporator and condenser seawater during operation of the one megawatt (1 MW) OTEC-1 test facility are reported. Although many halogenated compounds might be produced as a result of chlorination, the quantitative analyses in this study focused on volatile EPA priority pollutants. Bromoform is the compound specifically recognized as a potential pollutant. Its concentration may be indicative of other halogenated species.

  9. Assessment of the risk of transporting liquid chlorine by rail

    Energy Technology Data Exchange (ETDEWEB)

    Andrews, W.B.

    1980-03-01

    This report presents the risk of shipping liquid chlorine by rail. While chlorine is not an energy material, there are several benefits to studying chlorine transportation risks. First, chlorine, like energy materials, is widely used as a feedstock to industry. Second, it is the major purification agent in municipal water treatment systems and therefore, provides direct benefits to the public. Finally, other risk assessments have been completed for liquid chlorine shipments in the US and Europe, which provide a basis for comparison with this study. None of the previous PNL energy material risk assessments have had other studies for comparison. For these reasons, it was felt that a risk assessment of chlorine transportation by rail could provide information on chlorine risk levels, identify ways to reduce these risks and use previous studies on chlorine risks to assess the strengths and weaknesses of the PNL risk assessment methodology. The risk assessment methodology used in this study is summarized. The methodology is presented in the form of a risk assessment model which is constructed for ease of periodic updating of the data base so that the risk may be reevaluated as additional data become available. The report is sectioned to correspond to specific analysis steps identified in the model. The transport system and accident environment are described. The response of the transport system to accident environments is described. Release sequences are postulated and evaluated to determine both the likelihood and possible consequences of a release. Supportive data and analyses are given in the appendices. The risk assessment results are related to the year 1985 to allow a direct comparison with other reports in this series.

  10. Challenges in subsurface in situ remediation of chlorinated solvents

    OpenAIRE

    Broholm, Mette Martina; Fjordbøge, Annika Sidelmann; Christiansen, Camilla Maymann; Hønning, J.; B. H. Hansen; Nedergaard, L. W.; Kern, Kristina; Uthuppu, Basil; Jakobsen, Mogens Havsteen; Kjeldsen, Peter; Bjerg, Poul Løgstrup; Ottesen, L.

    2014-01-01

    Chlorinated solvent source zones in the subsurface pose a continuous threat to groundwater quality at many sites worldwide. In situ remediation of these sites is particularly challenging in heterogeneous fractured media and where the solvents are present as DNAPL. In situ remediation by chemical as well as biological degradation of chlorinated solvents is a contact sport and requires direct contact between the contaminant and the reactants and/or degrading microorganisms. In fractured geologi...

  11. Disinfection of swine wastewater using chlorine, ultraviolet light and ozone.

    Science.gov (United States)

    Macauley, John J; Qiang, Zhimin; Adams, Craig D; Surampalli, Rao; Mormile, Melanie R

    2006-06-01

    Veterinary antibiotics are widely used at concentrated animal feeding operations (CAFOs) to prevent disease and promote growth of livestock. However, the majority of antibiotics are excreted from animals in urine, feces, and manure. Consequently, the lagoons used to store these wastes can act as reservoirs of antibiotics and antibiotic-resistant bacteria. There is currently no regulation or control of these systems to prevent the spread of these bacteria and their genes for antibiotic resistance into other environments. This study was conducted to determine the disinfection potential of chlorine, ultraviolet light and ozone against swine lagoon bacteria. Results indicate that a chlorine dose of 30 mg/L could achieve a 2.2-3.4 log bacteria reduction in lagoon samples. However, increasing the dose of chlorine did not significantly enhance the disinfection activity due to the presence of chlorine-resistant bacteria. The chlorine resistant bacteria were identified to be closely related to Bacillus subtilis and Bacillus licheniformis. A significant percentage of lagoon bacteria were not susceptible to the four selected antibiotics: chlortetracycline, lincomycin, sulfamethazine and tetracycline (TET). However, the presence of both chlorine and TET could inactivate all bacteria in one lagoon sample. The disinfection potential of UV irradiation and ozone was also examined. Ultraviolet light was an effective bacterial disinfectant, but was unlikely to be economically viable due to its high energy requirements. At an ozone dose of 100 mg/L, the bacteria inactivation efficiency could reach 3.3-3.9 log.

  12. Carboranyl-Chlorin e6 as a Potent Antimicrobial Photosensitizer.

    Directory of Open Access Journals (Sweden)

    Elena O Omarova

    Full Text Available Antimicrobial photodynamic inactivation is currently being widely considered as alternative to antibiotic chemotherapy of infective diseases, attracting much attention to design of novel effective photosensitizers. Carboranyl-chlorin-e6 (the conjugate of chlorin e6 with carborane, applied here for the first time for antimicrobial photodynamic inactivation, appeared to be much stronger than chlorin e6 against Gram-positive bacteria, such as Bacillus subtilis, Staphyllococcus aureus and Mycobacterium sp. Confocal fluorescence spectroscopy and membrane leakage experiments indicated that bacteria cell death upon photodynamic treatment with carboranyl-chlorin-e6 is caused by loss of cell membrane integrity. The enhanced photobactericidal activity was attributed to the increased accumulation of the conjugate by bacterial cells, as evaluated both by centrifugation and fluorescence correlation spectroscopy. Gram-negative bacteria were rather resistant to antimicrobial photodynamic inactivation mediated by carboranyl-chlorin-e6. Unlike chlorin e6, the conjugate showed higher (compared to the wild-type strain dark toxicity with Escherichia coli ΔtolC mutant, deficient in TolC-requiring multidrug efflux transporters.

  13. Effect of wastewater chlorination on endocrine disruptor removal.

    Science.gov (United States)

    Noutsopoulos, C; Mamais, D; Samaras, V; Bouras, T; Marneri, M; Antoniou, K

    2013-01-01

    Endocrine disrupting chemicals (EDCs) are compounds of mainly anthropogenic origin that interfere with the endocrine system of animals and humans thus causing a series of disorders. Wastewater treatment plants are one of the major routes for transporting such chemicals to the water courses. In the context of this study, several chlorination batch tests were performed in order to assess the effectiveness of chlorination to remove bisphenol A (BPA), triclosan (TCS), nonylphenol (NP) and its ethoxylates (NP1EO and NP2EO) from secondary effluent. According to the results, an appreciable removal of NP, BPA and TCS to the order of 60-84% was observed as an effect of moderate chlorination doses. This was not the case for NP1EO and NP2EO as even at high chlorine doses, removal efficiencies were lower (37% for NP1EO and 52% for NP2EO). Removal efficiencies of NP, BPA and TCS are practically independent of contact time, although this was not the case for NP1EO and NP2EO. Based on toxicity experiments, it is anticipated that following chlorination of the target chemicals, production of more toxic metabolites is taking place. Therefore the effectiveness of chlorination to remove EDCs is questionable and more research is needed to guarantee safe wastewater reuse. PMID:23552244

  14. Prompt gamma analysis of chlorine in concrete for corrosion study.

    Science.gov (United States)

    Naqvi, A A; Nagadi, M M; Al-Amoudi, O S B

    2006-02-01

    Measurement of chlorine in concrete is very important for studying of corrosion of reinforcing steel in concrete. Corrosion of reinforcing steel is primarily ascribed to the penetration of chloride ions to the steel surface. Preventive measures for avoiding concrete structure reinforcement corrosion requires monitoring the chloride ion concentration in concrete so that its concentration does not exceed a threshold limit to initiate reinforcement concrete corrosion. An accelerator based prompt gamma neutron activation analysis (PGNAA) setup has been developed for non-destructive analysis of elemental composition of concrete samples. The setup has been used to measure chlorine concentration in concrete samples over a 1-3 wt% concentration range. Although a strong interference has been observed between the chlorine gamma-rays and calcium gamma-rays from concrete, the chlorine concentration in concrete samples has been successfully measured using the 1.164 and 7.643 MeV chlorine gamma-rays. The experimental data were compared with the results of the Monte Carlo simulations. An excellent agreement has been achieved between the experimental data and results of Monte Carlo simulations. The study has demonstrated the successful use of the accelerator-based PGNAA setup in non-destructive analysis of chlorine in concrete samples. PMID:16129605

  15. Site-selective photofragmentation of chlorinated polymeric films observed around the chlorine K-edge

    Energy Technology Data Exchange (ETDEWEB)

    Arantes, C., E-mail: csilva@inmetro.gov.br [Divisão de Metrologia de Materiais, Instituto Nacional de Metrologia, Qualidade e Tecnologia, Xerém 25250-020, Duque de Caxias, RJ (Brazil); Mendes, L.A.V. [Instituto de Física, Universidade Federal da Bahia, Ondina, 40210-340 Salvador, BA (Brazil); Pinho, R.R. [Departamento de Física-ICE, Universidade Federal de Juiz de Fora, Campus Universitário, 36036-330 Juiz de Fora, MG (Brazil); Ferreira, M. [PEMM/COPPE, Universidade Federal do Rio de Janeiro, Cidade Universitária, Ilha do Fundão, 21941-972 Rio de Janeiro, RJ (Brazil); Souza, G.G.B. de; Rocha, A.B.; Rocco, M.L.M. [Instituto de Química, Universidade Federal do Rio de Janeiro, Cidade Universitária, Ilha do Fundão, 21941-909 Rio de Janeiro, RJ (Brazil)

    2013-03-29

    Highlights: ► PVC and PVDC were studied by PSID and NEXAFS techniques at the Chlorine 1s-edge. ► PVC film presented isotope ratio of 3:1 in the PSID spectrum. ► Cl{sup +} ion yield curves reproduce the photoabsorption spectrum for both polymers. ► Site-selectivity of C–Cl bond breaking due to an efficient spectator Auger decay. - Abstract: Photon stimulated ion desorption (PSID) and Near-edge X-ray absorption fine structure (NEXAFS) studies have been performed on poly(vinyl chloride) (PVC) and poly(vinyl dichloride) (PVDC) around the chlorine 1s-edge. Experiments were performed using a synchrotron source operating in the single-bunch mode and a time-of-flight mass spectrometry for ion analysis. Cl{sup +} ion yields, as a function of the photon energy, reproduce the photoabsorption spectrum, showing significant increase at the 1s-resonance. Edge-jump ratios, defined as the ratio between edge-jumps (intensity ratio of the yields between above and below the absorption edge) of two different transitions, for Cl{sup +} ion yields were much higher than the equivalent electron yields, indicating site-selectivity in C–Cl bond breaking for both polymers, as a result of efficient spectator Auger decay. The expected isotope ratio of 3:1 for chlorine was measured for PVC. The interpretation of the NEXAFS spectrum was assisted by quantum mechanical calculations at a multireference perturbation theory level.

  16. Assessing chlorinated ethene degradation in a large scale contaminant plume by dual carbon–chlorine isotope analysis and quantitative PCR

    DEFF Research Database (Denmark)

    Hunkeler, D.; Abe, Y.; Broholm, Mette Martina;

    2011-01-01

    DCE. The significant enrichment of 13C in VC indicates that VC was transformed further, although the mechanismcould not be determined. The transformation of cDCEwas the rate limiting step as no accumulation of VC occurred. In summary, the study demonstrates that carbon–chlorine isotope analysis and qPCR combinedwith......The fate of chlorinated ethenes in a large contaminant plume originating from a tetrachloroethene (PCE) source in a sandy aquifer in Denmark was investigated using novel methods including compound-specific carbon and chlorine isotope analysis and quantitative real-time polymerase chain reaction (q......) concentrations remained low (b1 μg/L) and ethene was not observed. The correlated shift of carbon and chlorine isotope ratios of cDCE by 8 and 3.9‰, respectively, the detection of Dehaloccocides sp genes, and strongly reducing conditions in this zone provide strong evidence for reductive dechlorination of c...

  17. Inactivation of antibiotic resistance genes in municipal wastewater effluent by chlorination and sequential UV/chlorination disinfection

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Yingying; Zhuang, Yao; Geng, Jinju, E-mail: jjgeng@nju.edu.cn; Ren, Hongqiang, E-mail: hqren@nju.edu.cn; Zhang, Yan; Ding, Lili; Xu, Ke

    2015-04-15

    This study investigated disinfection methods including chlorination, ultraviolet (UV) irradiation and sequential UV/chlorination treatment on the inactivation of antibiotic resistance genes (ARGs). ARGs including sul1, tetX, tetG, intI1, and 16S rRNA genes in municipal wastewater treatment plant (MWTP) effluent were examined. The results indicated a positive correlation between the removal of ARGs and chlorine dosage (p = 0.007–0.014, n = 6),as well as contact time (p = 0.0001, n = 10). Greater free chlorine (FC) dosage leads to higher removal for all the genes and the maximum removal (1.30–1.49 logs) could be achieved at FC dosage of 30 mg L{sup −1}. The transformation kinetic data for ARGs removal (log C{sub 0} / C) followed the second-order reaction kinetic model with FC dosage (R{sup 2} = 0.6829–0.9999) and contact time (R{sup 2} = 0.7353–8634), respectively. Higher ammonia nitrogen (NH{sub 3}–N) concentration was found to lead to lower removal of ARGs at the same chlorine dosage. When the applied Cl{sub 2}:NH{sub 3}–N ratio was over 7.6:1, a significant reduction of ARGs (1.20–1.49 logs) was achieved. By using single UV irradiation, the log removal values of tetX and 16Ss rRNA genes were 0.58 and 0.60, respectively, while other genes were 0.36–0.40 at a fluence of 249.5 mJ cm{sup −2}, which was observed to be less effective than chlorination. With sequential UV/chlorination treatment, 0.006 to 0.31 log synergy values of target genes were observed under different operation parameters. - Highlights: • Chlorine is more effective than UV irradiation in removing ARGs from MWTP effluent. • The chlorination reaction followed the second-order reaction kinetic model. • Higher NH{sub 3}–N contents result in lower ARGs removal in the chlorination process. • FC is more effective than CC on the inactivation of ARGs. • UV irradiation followed by chlorination shows high efficiency in removing ARGs.

  18. Inactivation of antibiotic resistance genes in municipal wastewater effluent by chlorination and sequential UV/chlorination disinfection

    International Nuclear Information System (INIS)

    This study investigated disinfection methods including chlorination, ultraviolet (UV) irradiation and sequential UV/chlorination treatment on the inactivation of antibiotic resistance genes (ARGs). ARGs including sul1, tetX, tetG, intI1, and 16S rRNA genes in municipal wastewater treatment plant (MWTP) effluent were examined. The results indicated a positive correlation between the removal of ARGs and chlorine dosage (p = 0.007–0.014, n = 6),as well as contact time (p = 0.0001, n = 10). Greater free chlorine (FC) dosage leads to higher removal for all the genes and the maximum removal (1.30–1.49 logs) could be achieved at FC dosage of 30 mg L−1. The transformation kinetic data for ARGs removal (log C0 / C) followed the second-order reaction kinetic model with FC dosage (R2 = 0.6829–0.9999) and contact time (R2 = 0.7353–8634), respectively. Higher ammonia nitrogen (NH3–N) concentration was found to lead to lower removal of ARGs at the same chlorine dosage. When the applied Cl2:NH3–N ratio was over 7.6:1, a significant reduction of ARGs (1.20–1.49 logs) was achieved. By using single UV irradiation, the log removal values of tetX and 16Ss rRNA genes were 0.58 and 0.60, respectively, while other genes were 0.36–0.40 at a fluence of 249.5 mJ cm−2, which was observed to be less effective than chlorination. With sequential UV/chlorination treatment, 0.006 to 0.31 log synergy values of target genes were observed under different operation parameters. - Highlights: • Chlorine is more effective than UV irradiation in removing ARGs from MWTP effluent. • The chlorination reaction followed the second-order reaction kinetic model. • Higher NH3–N contents result in lower ARGs removal in the chlorination process. • FC is more effective than CC on the inactivation of ARGs. • UV irradiation followed by chlorination shows high efficiency in removing ARGs

  19. Novel Lead dioxide-Graphite-Polymer composite anode for electrochemical chlorine generation

    International Nuclear Information System (INIS)

    Graphical abstract: Display Omitted -- Highlights: • Synthesis of tetragonal β-PbO2 impregnated graphite powder (G-PbO2). • Fabrication of polymer composite disc (G-PbO2-PMMA). • G-PbO2-PMMA electrode surface containing catalytic amounts of β-PbO2. • Better performance of G-PbO2-PMMA anode vs. Pt for chlorine evolution. • Efficient, low-cost anode for indirect oxidation of pollutants. -- Abstract: Lead dioxide coated graphite powder (G-PbO2) was synthesized using in-situ wet chemical synthesis method. Phase identification by X-ray diffraction (XRD) revealed the successful synthesis of G-PbO2 powder, containing β-PbO2. This powder was mixed with poly-methyl methacrylate (PMMA) and molded into circular discs for use as electrodes conveniently. The surface morphology and composition of the polymer composite (G-PbO2-PMMA) electrodes was characterized using SEM, EDXA and XPS. Electron transfer dynamics at the G-PbO2-PMMA electrode were examined using standard ferro-ferricyanide redox couple, Fe(CN)63−/4−, which displayed peak-to-peak separation of ∼71 mV. The electrochemical evolution of chlorine at G-PbO2-PMMA anode was also studied which showed favorableshift in the value of oxidation peak potential by ∼ 116 mV relative to Pt electrode. The concentration of total chlorine in solution was determined as a function of number of cyclic voltammetric scans at different scan rates. The observed concentration of the dissolved Cl2 was 23 mg L−1 (G-PbO2-PMMA, 5 mVs−1, 50CV cycles) and 15 mg L−1(Pt, 5 mVs−1, 50CV cycles). The performance of G-PbO2-PMMA with respect to chlorine evolution was found to be better compared with that of Pt electrode. The electron transfer at the lead dioxide coated graphite is found to be facile and the G-PbO2-PMMA is inferred to be good anode material for efficient Cl2 evolution

  20. Hydrogen-chlorine fuel cell for production of hydrochloric acid and electric power : chlorine kinetics and cell design

    OpenAIRE

    Thomassen, Magnus Skinlo

    2005-01-01

    This thesis work is the continuation and final part of a joint project between the Department of Materials Technology, NTNU and Norsk Hydro Research Center in Porsgrunn, looking at the possibility of using fuel cells for production of hydrogen chloride and electric power. The experimental work encompass an evaluation of three hydrogen - chlorine fuel cell design concepts, development and implementation of a mathematical fuel cell model and a kinetic study of the chlorine reduction reaction. T...

  1. Efficacy of Nucleic Acid Probes for Detection of Poliovirus in Water Disinfected by Chlorine, Chlorine Dioxide, Ozone, and UV Radiation

    OpenAIRE

    Moore, Norman J.; Margolin, Aaron B.

    1994-01-01

    MilliQ water was inoculated with poliovirus type 1 strain LSc-1 and was treated with disinfectants, including chlorine, chlorine dioxide, ozone, and UV light. No relationship between probes and plaque assays were seen, demonstrating that viral nucleic acids were not destroyed. These findings suggest that nucleic acid probes cannot distinguish between infectious and noninfectious viruses and cannot be used in the evaluation of treated waters.

  2. Efficacy of chlorine, acidic electrolyzed water and aqueous chlorine dioxide solutions to decontaminate Escherichia coli O157:H7 from lettuce leaves

    Science.gov (United States)

    This study compared the efficacy of chlorine (20 – 200 ppm), acidic electrolyzed water (50 ppm chlorine, pH 2.6), acidified sodium chlorite (20 – 200 ppm chlorite ion concentration, Sanova), and aqueous chlorine dioxide (20 – 200 ppm chlorite ion concentration, TriNova) washes in reducing population...

  3. Chlorine Stabilizer T-128 enhances efficacy of chlorine against cross contamination by E. coli O157:H7 and Salmonella in fresh-cut lettuce processing

    Science.gov (United States)

    During fresh produce processing, organic materials released from cut tissues can rapidly react with free chlorine in the wash solution, leading to the potential survival of foodborne bacterial pathogens and cross-contamination when the free chlorine is depleted. A reported chlorine stabilizer, T128...

  4. Role of alloying elements and carbides in the chlorine-induced corrosion of steels and alloys

    Directory of Open Access Journals (Sweden)

    Hans Jürgen Grabke

    2004-03-01

    Full Text Available The high temperature corrosion of steels and Ni-base alloys in oxidizing and chloridizing environments is of practical interest in relation to problems in waste incineration plants and power plants using Cl containing fuels. The behaviour of the most important alloying elements Fe, Cr, Ni, Mo, Mn, Si, Al upon corrosion in an oxidizing and chloridizing atmosphere was elucidated: the reactions and kinetics can be largely understood on the base of thermodynamic data, i.e. free energy of chloride formation, vapor pressure of the chlorides and oxygen pressure pO2 needed for the conversion chlorides -> oxides. The mechanism is described by 'active oxidation', comprising inward penetration of chlorine into the scale, formation of chlorides at the oxide/metal interface, evaporation of the chlorides and conversion of the evaporating chlorides into oxides, which occurs in more or less distance from the surface (depending on pO2. This process leads to loose, fragile, multilayered oxides which are unprotective (therefore: active oxidation. Fe and Cr are rapidly transferred into such scale, Ni and Mo are relatively resistant. In many cases, the grain boundaries of the materials are strongly attacked, this is due to a susceptibility of chromium carbides to chloridation. In contrast the carbides Mo2C, TiC and NbC are less attacked than the matrix. Alloys on the basis Fe-Cr-Si proved to be rather resistant, and the alloying elements Ni and Mo clearly retard the attack in an oxidizing and chloridizing environment.

  5. Chemical speciation of chlorine in atmospheric aerosol samples by high-resolution proton induced X-ray emission spectroscopy

    International Nuclear Information System (INIS)

    Chlorine is a main elemental component of atmospheric particulate matter (APM). The knowledge of the chemical form of chlorine is of primary importance for source apportionment and for estimation of health effects of APM. In this work the applicability of high-resolution wavelength dispersive proton induced X-ray emission (PIXE) spectroscopy for chemical speciation of chlorine in fine fraction atmospheric aerosols is studied. A Johansson-type crystal spectrometer with energy resolution below the natural linewidth of Cl K lines was used to record the high-resolution Kα and Kβ proton induced spectra of several reference Cl compounds and two atmospheric aerosol samples, which were collected for conventional PIXE analysis. The Kα spectra which refers to the oxidation state, showed very minor differences due to the high electronegativity of Cl. However, the Kβ spectra exhibited pronounced chemical effects which were significant enough to perform chemical speciation. The major chlorine component in two fine fraction aerosol samples collected during a 2010 winter campaign in Budapest was clearly identified as NaCl by comparing the high-resolution Cl Kβ spectra from the aerosol samples with the corresponding reference spectra. This work demonstrates the feasibility of high-resolution PIXE method for chemical speciation of Cl in aerosols. - Highlights: ► Chemical specation of Cl in aerosol samples by high resolution PIXE spectroscopy. ► Fine structure of Kα and Kβ lines of reference compounds and APM samples was given. ► Kα spectra were well aligned with each other confirming the same Cl oxidation state. ► Pronounced chemical effects were observed in the Kβ spectra. ► We showed that chemical speciation of Cl was possible on thin aerosol samples

  6. Analysis of residual chlorine in simple drinking water distribution system with intermittent water supply

    Science.gov (United States)

    Goyal, Roopali V.; Patel, H. M.

    2015-09-01

    Knowledge of residual chlorine concentration at various locations in drinking water distribution system is essential final check to the quality of water supplied to the consumers. This paper presents a methodology to find out the residual chlorine concentration at various locations in simple branch network by integrating the hydraulic and water quality model using first-order chlorine decay equation with booster chlorination nodes for intermittent water supply. The explicit equations are developed to compute the residual chlorine in network with a long distribution pipe line at critical nodes. These equations are applicable to Indian conditions where intermittent water supply is the most common system of water supply. It is observed that in intermittent water supply, the residual chlorine at farthest node is sensitive to water supply hours and travelling time of chlorine. Thus, the travelling time of chlorine can be considered to justify the requirement of booster chlorination for intermittent water supply.

  7. Investigation of the oxidation of hydrochloric acid in scrubbing solutions containing hydrogen peroxide

    International Nuclear Information System (INIS)

    Oxidation and absorption of nitrogen oxides by a solution containing sulphuric, nitric acids and hydrogen peroxide have been investigated. The oxidation of nitric oxide is dependent among others on hydrogen peroxide concentration total acidity and temperature. The absorption of N O2 by the scrubbing solution (H2 S O4,H N O3 and H2 O2) in all cases studied is not less than 98%. The oxidation of chloride into chlorine gas increases as the concentration of each of hydrochloric acid, nitric oxide and nitric acid increases. On the other hand as the concentration of hydrogen peroxide increases the amount of chlorine gas decreases. The results show that the oxidation of chloride into chlorine gas is mainly due to nitrogen dioxide. 7 fig., 2 tab

  8. Development of a Site-Specific Kinetic Model for Chlorine Decay and the Formation of Chlorination By-Products in Seawater

    Directory of Open Access Journals (Sweden)

    Suhur Saeed

    2015-07-01

    Full Text Available Chlorine is used commonly to prevent biofouling in cooling water systems. The addition of chlorine poses environmental risks in natural systems due to its tendency to form chlorination by-products (CBPs when exposed to naturally-occurring organic matter (NOM. Some of these CBPs can pose toxic risks to aquatic and benthic species in the receiving waters. It is, therefore, important to study the fate of residual chlorine and CBPs to fully understand the potential impacts of chlorination to the environment. The goal of this study was to develop improved predictions of how chlorine and CBP concentrations in seawater vary with time, chlorine dose and temperature. In the present study, chlorination of once-through cooling water at Ras Laffan Industrial City (RLIC, Qatar, was studied by collecting unchlorinated seawater from the RLIC cooling water system intake, treating it with chlorine and measuring time series of chlorine and CBP concentrations. Multiple-rate exponential curves were used to represent fast and slow chlorine decay and CBP formation, and site-specific chlorine kinetic relationships were developed. Through extensive analysis of laboratory measurements, it was found that only some of the control parameters identified in the literature were important for predicting residual chlorine and CBP concentrations for this specific location. The new kinetic relationships were able to significantly improve the predictability and validity of Generalized Environmental Modeling System for Surfacewaters (GEMSS-chlorine kinetics module (CKM, a three-dimensional hydrodynamic and chlorine kinetics and transport model when applied for RLIC outfall studies using actual field measurements.

  9. Structural modeling and intermolecular correlation of liquid chlorine dioxide

    International Nuclear Information System (INIS)

    Chlorine dioxide (ClO2) is water-soluble yellow gas at room temperature. It has long been used as a disinfectant of tap water and various commodities owing to its strong oxidizing activity against various microbial proteins. The oxidizing activity is believed to be due to the presence of unpaired electron in its molecular orbital. Despite wealth of physicochemical studies of gaseous ClO2, little is known about liquid ClO2, especially about fine molecular structure and intermolecular interactions of liquid ClO2. The purpose of this study is to elucidate the fine structure and intermolecular orientations of ClO2 molecules in its liquid state using a high-energy X-ray diffraction technique. The measurements of liquid ClO2 were carried out at -50 to 0 degree Celsius using a two-axis diffractometer installed at the BL04B2 beamline in the third-generation synchrotron radiation facility SPring-8 (Hyogo, Japan). The incident X-ray beamline was 113.4 keV in energy and 0.1093 Armstrong in wavelength from a Si(111) monochromator with the third harmonic reflection. Liquid ClO2 held in a quartz capillary tube was placed in a temperature-controlled vacuum chamber. We obtained a structure factor S(Q) to a range of Q = 0.3-30 Amstrong-1 and a pair distribution function g(r) upon Fourier transform of the S(Q). The total g(r) showed peaks at 1.46, 2.08, 2.48, 3.16 and 4.24 Armstrong. From intramolecular bond lengths of 1.46 Armstrong for Cl-O and 2.48 Armstrong for O-O, O-Cl-O bond angle was estimated to be 116.1 degrees. Peaks at 3.16 and 4.24 Armstrong in the total g(r) strongly indicate presence of specific intermolecular orientations of ClO2 molecules that are distinct from those observed as a dimer in the solid phase ClO2. This view was further supported by molecular simulation using a reverse Monte Carlo method (RMC). (author)

  10. Can chlorination co-select antibiotic-resistance genes?

    Science.gov (United States)

    Lin, Wenfang; Zhang, Menglu; Zhang, Shenghua; Yu, Xin

    2016-08-01

    Selective pressures, such as chemical or heavy metal pollution, may co-select for bacterial antibiotic resistance in the environment. However, whether chlorination in water treatment can co-select antibiotic-resistant bacteria is controversial. In this study, high capacity quantitative polymerase chain reaction (qPCR) analysis was applied to target almost all known antibiotic-resistance genes (ARGs) (282 types) and 13 mobile genetic elements (MGEs) in bacteria detected in secondary effluents from a municipal wastewater treatment plant after chlorination. The results revealed that 125 unique ARGs were detected in non-chlorinated samples, and the number decreased (79-91 types) as the chlorine concentration was increased. Moreover, 7.49 × 10(4)-3.92 × 10(7) copies/100 ml water reduction of ARGs occurred with 4 mg Cl2/l. Considering the relative abundance of ARGs (i.e., ARG copies normalized to 16S rRNA gene copies), 119 ARGs decreased in response to chlorination, whereas only six ARGs, such as dfrA1, tetPB-03, tetPA, ampC-04, tetA-02, and erm(36), were potentially enriched by 10.90-, 10.06-, 8.63-, 6.86-, 3.77-, and 1.09-fold, respectively. Furthermore, the relative abundance of 12 detected MGEs was lower after chlorination. Therefore, chlorination was effective in reducing ARGs and MGEs rather than co-selecting them. PMID:27192478

  11. Cold Incineration of Chlorophenols in Aqueous Solution by Advanced Electrochemical Process Electro-Fenton. Effect of Number and Position of Chlorine Atoms on the Degradation Kinetics

    Science.gov (United States)

    Oturan, Nihal; Panizza, Marco; Oturan, Mehmet A.

    2009-09-01

    This study reports the kinetics of the degradation of several chlorophenols (CPs), such as monochlorophenols (2-chlorophenol and 4-chlorophenol), dichlorophenols (2,4-dichlorophenol and 2,6- dichlorophenol), trichlorophenols (2,3,5- trichlorophenol and 2,4,5-trichlorophenol), 2,3,5,6-tetrachlorophenol, and pentachlorophenol, by the electro-Fenton process using a carbon felt cathode and a Pt anode. The effect of number and the position of the chlorine atoms in the aromatic ring on the oxidative degradation rate was evaluated and discussed. The oxidation reaction of all the CPs with hydroxyl radicals evidenced a pseudo-first-order kinetics and the rate constant decreased with increasing the number of chlorine atoms. The absolute rate constant of second-order reaction kinetics between CPs and •OH was determined by the competition kinetics method in the range of (3.56-7.75) × 109 M-1 s-1 and follows the same sequence of the apparent rate constants. The mineralization of several CPs and of a mixture of all CPs under study was monitored by the total organic carbon (TOC) removal and the chlorine release during mineralization was followed by ion chromatography. Our results demonstrated that more chlorinated phenols are more difficult to mineralize; however for all the tested CPs, almost quantitative release of chloride ions was obtained after 6 h of treatment.

  12. Electrochemical reduction characteristics and the mechanism of chlorinated hydrocarbons at the copper electrode

    Institute of Scientific and Technical Information of China (English)

    XU Wenying; GAO Tingyao; ZHOU Rongfeng; MA Lumin

    2007-01-01

    The electrochemical reduction characteristies of chlorinated hyrdrocarbons were investigated by cyclic voltammetry technique.The reduction mechanism and activity of the chlorinated hydrocarbons at the copper electrode were explored.The relationship between the structure of chlorinated hydrocarbons and their reductive activity were discussed.The experimental results showed that chlorinated alkanes and a portion of chlorinated aromatic hydrocarbons could be reduced directly at the copper electrode.However,chlorinated aromatic hydrocarbons were not easy to reduce at the copper electrode.The results provided a theoretical basis for the catalyzed iron inner electrolysis method.

  13. Study on metal corrosion caused by chlorine dioxide of various purities

    Institute of Scientific and Technical Information of China (English)

    崔崇威; 黄君礼; 许晶

    2004-01-01

    Weight lost method was used to comparatively study the corrosion behavior of four different metals under the dosage of chlorine dioxide, chlorine and their mixture respectively. The experimental results indicated that chlorine causes the most serious corrosion of carbon steel, and the higher the concentration of chlorine, the more serious the corrosion. On the contras, metals corrosion is the least serious in the case of chlorine dioxide.The results further revealed that chlorine dioxide is the most effective water treatment reagent, making it the best choice to use extensively in circulated cooling water disinfection and corrosion control.

  14. Fenton process for degradation of selected chlorinated aliphatic hydrocarbons exemplified by trichloroethylene, 1,1-dichloroethylene and chloroform

    Institute of Scientific and Technical Information of China (English)

    Zhimin QIANG; Weiwei BEN; ChinPao HUANG

    2008-01-01

    The degradation of selected chlorinated ali-phatic hydrocarbons (CAHs) exemplified by trichloroethy-lene (TCE), 1,1-dichloroethylene (DCE), and chloroform (CF) was investigated with Fenton oxidation process. The results indicate that the degradation rate was primarily affected by the chemical structures of organic contami-nants. Hydroxyl radicals (·OH) preferred to attack the organic contaminants with an electron-rich structure such as chlorinated alkenes (i.e., TCE and DCE). The dosing mode of Fenton's reagent, particularly of Fe2+, significantly affected the degradation efficiency of studied organic compound. A new "time-squared" kinetic model, C = Coexp(-kobst2), was developed to express the degrada-tion kinetics of selected CAHs. This model was applicable to TCE and DCE, but inapplicable to CF due to their varied reaction rate constants towards ·OH. Chloride release was monitored to examine the degree of dechlorina- tion during the oxidation of selected CAHs. TCE was more easily dechlorinated than DCE and CF. Dichloroacetic acid (DCAA) was identified as the major reaction intermediate in the oxidation of TCE, which could be completely removed as the reaction proceeded. No reaction intermedi- ates or byproducts were identified in the oxidation of DCE and CF. Based on the identified intermediate, the reaction mechanism of TCE with Fenton's reagent was proposed.

  15. Chemical aspects of incinerating highly chlorinated and actinide α contaminated organic waste: application to the Iris process

    International Nuclear Information System (INIS)

    A fraction of the waste produced by nuclear activities is combustible, and thus suitable for incineration to produce gases, ash and fines. A typical composition representative of actual organic waste mixtures was defined for the purpose of investigating possible heat treatment processes; the composition is identified according to components Table 1 and elements Table II. The high polyvinyl chloride (PVC) content is responsible for the high chlorine potential in the process equipment. The quantity and quality of the resulting solid residue depends entirely on the inorganic load of the organic waste, whose behavior is entirely conditioned by the process conditions. For example, pure polyethylene is totally converted to gases (water and carbon dioxide), while the composition shown in Table II produces a range of oxides and chlorides. The high chlorine content results in partial chlorination of the inorganic compounds, but can also lead to interactions with the process equipment. The temperature dependent variation of the chlorination equilibrium constants of various metals clearly shows that all the elements of technological alloys may be subject to active corrosion by hydrochloric acid. However, the corresponding oxides-notably alumina-are much less sensitive to corrosion; aluminum-based alloys are therefore preferred for incinerator construction and to limit corrosion by hydrochloric acid. Thermodynamic and kinetic studies led to the development of the IRIS three-step process. Gas emissions occurring during processing of solid materials are completely oxidized in the after-burning step at 1100 deg C, and are then ducted to a HERA filtration system capable of retaining all the actinide α radionuclides. Although corrosion-related problems are attenuated in the two-step process chlorine can combine with the inorganic waste material to form chlorides with potentially damaging effects on the system; this is the case for zinc chloride and for volatile chlorides in

  16. Inactivation of antibiotic resistance genes in municipal wastewater effluent by chlorination and sequential UV/chlorination disinfection.

    Science.gov (United States)

    Zhang, Yingying; Zhuang, Yao; Geng, Jinju; Ren, Hongqiang; Zhang, Yan; Ding, Lili; Xu, Ke

    2015-04-15

    This study investigated disinfection methods including chlorination, ultraviolet (UV) irradiation and sequential UV/chlorination treatment on the inactivation of antibiotic resistance genes (ARGs). ARGs including sul1, tetX, tetG, intI1, and 16S rRNA genes in municipal wastewater treatment plant (MWTP) effluent were examined. The results indicated a positive correlation between the removal of ARGs and chlorine dosage (p=0.007-0.014, n=6),as well as contact time (p=0.0001, n=10). Greater free chlorine (FC) dosage leads to higher removal for all the genes and the maximum removal (1.30-1.49 logs) could be achieved at FC dosage of 30 mg L(-1). The transformation kinetic data for ARGs removal (log C0/C) followed the second-order reaction kinetic model with FC dosage (R(2)=0.6829-0.9999) and contact time (R(2)=0.7353-8634), respectively. Higher ammonia nitrogen (NH3-N) concentration was found to lead to lower removal of ARGs at the same chlorine dosage. When the applied Cl2:NH3-N ratio was over 7.6:1, a significant reduction of ARGs (1.20-1.49 logs) was achieved. By using single UV irradiation, the log removal values of tetX and 16Ss rRNA genes were 0.58 and 0.60, respectively, while other genes were 0.36-0.40 at a fluence of 249.5 mJ cm(-2), which was observed to be less effective than chlorination. With sequential UV/chlorination treatment, 0.006 to 0.31 log synergy values of target genes were observed under different operation parameters.

  17. Rapid Determination of HAAs Formation Potential of the Reaction of Humic Acid with Chlorine or Chlorine Dioxide

    Institute of Scientific and Technical Information of China (English)

    ZHU Zhi-liang; GE Yuan-xin; ZHANG Rong-hua; MA Hong-mei; HAO Jian-fu

    2007-01-01

    On the basis of gas chromatography(GC) coupled with a short capillary column and an electron capture detector(ECD), a simple and rapid method for the determination of five haloacetic acids(HAAs) in drinking water was developed by the optimization of derivation conditions and the modification of gas chromatographic program. HAAs formation potential(HAAFP) of the reaction of humic acid with chlorine was determined via this method. The major advantages of the method are the simplicity of chromatographic temperature program and the short run time of GC. Dichloroacetic acid(DCAA) and Trichloroacetic acid(TCAA), which were detected in the determination of HAAFP, were rapidly formed in the first 72 h of the reaction of humic acid with chlorine. HAAFP of the reaction of humic acid with chlorine increased with the increase in the concentrations of humic acid and chlorine. The average HAAFP of the reaction of humic acid with chlorine was 39.9 μg/mg TOC under the experimental conditions. When the concentration of humic acid was 4 mg/L, the concentration of HAAs, which were produced in the reaction of humic acid with chorine, may exceed MCL of 60 μg/L HAAs as the water quality standards for urban water supply of China and the first stage of US EPA disinfection/disinfection by-products(D/DBP) rule; when the concentration of humic acid was 2 mg/L, the concentration of HAAs may exceed MCL of 30 μg/L HAAs for the second stage of US EPA D/DBP rule. When humic acid was reacted with chlorine dioxide, only DCAA was detected with a maximum concentration of 3.3 μg/L at a humic acid content of 6 mg/L. It was demonstrated that the substitution of chlorine dioxide for chorine may entirely or partly control the formation of HAAs and effectively reduce the health risk associated with disinfected drinking water.

  18. Immobilization of chlorine dioxide modified cells for uranium absorption

    International Nuclear Information System (INIS)

    There has been a trend towards the use of microorganisms to recover metals from industrial wastewater, for which various methods have been reported to be used to improve microorganism adsorption characteristics such as absorption capacity, tolerance and reusability. In present study, chlorine dioxide(ClO2), a high-efficiency, low toxicity and environment-benign disinfectant, was first reported to be used for microorganism surface modification. The chlorine dioxide modified cells demonstrated a 10.1% higher uranium adsorption capacity than control ones. FTIR analysis indicated that several cell surface groups are involved in the uranium adsorption and cell surface modification. The modified cells were further immobilized on a carboxymethylcellulose (CMC) matrix to improve their reusability. The cell-immobilized adsorbent could be employed either in a high concentration system to move vast UO22+ ions or in a low concentration system to purify UO22+ contaminated water thoroughly, and could be repeatedly used in multiple adsorption-desorption cycles with about 90% adsorption capacity maintained after seven cycles. - Highlights: • Chlorine dioxide was first reported to be used for microorganism surface modification. • The chlorine dioxide modified cells demonstrated a 10.1% higher uranium adsorption capacity than control ones. • The chlorine dioxide modified cells were further immobilized by carboxymethylcellulose to improve their reusability

  19. Biofilm formation by Pseudoalteromonas ruthenica and its removal by chlorine.

    Science.gov (United States)

    Saravanan, Periasamy; Nancharaiah, Y Venkata; Venugopalan, Vayalam P; Rao, T Subba; Jayachandran, Seetharaman

    2006-01-01

    The distribution of a recently described marine bacterium, SBT 033 GenBank Accession No. AY723742), Pseudoalteromonas ruthenica, at the seawater intake point, outfall and mixing point of an atomic power plant is described, and its ability to form biofilm was investigated. The effectiveness of the antifouling biocide chlorine in the inactivation of planktonic as well as biofilm cells of P. ruthenica was studied in the laboratory. The results show that the planktonic cells were more readily inactivated than the cells enclosed in a biofilm matrix. Viable counting showed that P. ruthenica cells in biofilms were up to 10 times more resistant to chlorine than those in liquid suspension. Using confocal laser scanning microscopy it was shown that significant detachment of P. ruthenica biofilm developed on a glass substratum could be accomplished by treatment with a dose of 1 mg l-1 chlorine. Chlorine-induced detachment led to a significant reduction in biofilm thickness (up to 69%) and substratum coverage (up to 61%), after 5-min contact time. The results show that P. ruthenica has a remarkable ability to form biofilms but chlorine, a common biocide, can be used to effectively kill and detach these biofilms. PMID:17178570

  20. MECHANISM OF CHLORATE FORMATION IN CHLORINE DIOIXDE DELIGNIFICATION

    Institute of Scientific and Technical Information of China (English)

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

    2004-01-01

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

  1. Bacterial repopulation of drinking water pipe walls after chlorination.

    Science.gov (United States)

    Mathieu, Laurence; Francius, Grégory; El Zein, Racha; Angel, Edith; Block, Jean-Claude

    2016-09-01

    The short-term kinetics of bacterial repopulation were evaluated after chlorination of high-density polyethylene (HDPE) colonized with drinking water biofilms and compared with bare HDPE surfaces. The effect of chlorination was partial as a residual biofilm persisted and was time-limited as repopulation occurred immediately after water resupply. The total number of bacteria reached the same levels on both the bare and chlorinated biofilm-fouled HDPE after a seven-day exposure to drinking water. Due to the presence of a residual biofilm, the hydrophobicity of chlorinated biofilm-fouled surface exhibited much lower adhesion forces (2.1 nN) compared to bare surfaces (8.9 nN). This could explain the rapid repopulation after chlorination, with a twofold faster bacterial accumulation rate on the bare HDPE surface. γ-Proteobacteria dominated the early stages of repopulation of both surfaces and a shift in the dominance occurred over the colonization time. Such observations define a timescale for cleaning frequency in industrial environments and guidelines for a rinsing procedure using drinking water. PMID:27483985

  2. Biofouling control: Bacterial quorum quenching versus chlorination in membrane bioreactors.

    Science.gov (United States)

    Weerasekara, Nuwan A; Choo, Kwang-Ho; Lee, Chung-Hak

    2016-10-15

    Biofilm formation (biofouling) induced via cell-to-cell communication (quorum sensing) causes problems in membrane filtration processes. Chorine is one of the most common chemicals used to interfere with biofouling; however, biofouling control is challenging because it is a natural process. This study demonstrates biofouling control for submerged hollow fiber membranes in membrane bioreactors by means of bacterial quorum quenching (QQ) using Rhodococcus sp. BH4 with chemically enhanced backwashing. This is the first trial to bring QQ alongside chlorine injection into practice. A high chlorine dose (100 mg/L as Cl2) to the system is insufficient for preventing biofouling, but addition of the QQ bacterium is effective for disrupting biofouling that cannot be achieved by chlorination alone. QQ reduces the biologically induced metal precipitate and extracellular biopolymer levels in the biofilm, and biofouling is significantly delayed when QQ is applied in addition to chlorine dosing. QQ with chlorine injection gives synergistic effects on reducing physically and chemically reversible fouling resistances while saving substantial filtration energy. Manipulating microbial community functions with chemical treatment is an attractive tool for biofilm dispersal in membrane bioreactors.

  3. Chlorinated organic pesticides in marketed food: Barcelona, 2001-06

    International Nuclear Information System (INIS)

    This paper reports concentration levels of 22 chlorinated organic compounds (both primary compounds and metabolites) in food marketed in the city of Barcelona (Catalonia, Spain) in 2001-06. Samples included meat products, fish and seafood, eggs, milk and dairy, vegetal oils, cereal products and derivates, vegetables, fresh fruits, dry fruits, spices, formula and baby food, tea and wine. Levels of chlorinated organic compounds were determined by gas chromatography with selective detectors: electron capture (ECD), flame photometric (FPD) and confirmation with mass-spectrometry. Chlorinated organic pesticides were detected in 7 of the 1,484 samples analyzed in the 2001-06 period (0.5%): 1 dairy product, 1 fruit, 1 olive oil and 4 vegetables. Specific pesticides detected are lindane and endosulfan α, β or sulphate. A decrease in both the proportion of samples with detectable residues and in the variety of chlorinated pesticides found is visible when comparing these results with those of the previous 1989-2000 period. These results suggest the gradual disappearance of regulated chlorinated organic pesticides as a consequence of the growing worldwide implementation of current regulatory agreements

  4. Chlorination byproducts, their toxicodynamics and removal from drinking water.

    Science.gov (United States)

    Gopal, Krishna; Tripathy, Sushree Swarupa; Bersillon, Jean Luc; Dubey, Shashi Prabha

    2007-02-01

    No doubt that chlorination has been successfully used for the control of water borne infections diseases for more than a century. However identification of chlorination byproducts (CBPs) and incidences of potential health hazards created a major issue on the balancing of the toxicodynamics of the chemical species and risk from pathogenic microbes in the supply of drinking water. There have been epidemiological evidences of close relationship between its exposure and adverse outcomes particularly the cancers of vital organs in human beings. Halogenated trihalomethanes (THMs) and haloacetic acids (HAAs) are two major classes of disinfection byproducts (DBPs) commonly found in waters disinfected with chlorine. The total concentration of trihalomethanes and the formation of individual THM species in chlorinated water strongly depend on the composition of the raw water, on operational parameters and on the occurrence of residual chlorine in the distribution system. Attempts have been made to develop predictive models to establish the production and kinetics of THM formations. These models may be useful for operational purposes during water treatment and water quality management. It is also suggested to explore some biomarkers for determination of DBP production. Various methods have been suggested which include adsorption on activated carbons, coagulation with polymer, alum, lime or iron, sulfates, ion exchange and membrane process for the removal of DBPs. Thus in order to reduce the public health risk from these toxic compounds regulation must be inforced for the implementation of guideline values to lower the allowable concentrations or exposure.

  5. Inactivation of Aspergillus flavus in drinking water after treatment with UV irradiation followed by chlorination

    Energy Technology Data Exchange (ETDEWEB)

    Al-Gabr, Hamid Mohammad [Key Laboratory of Urban Environment and Health, Institute of Urban Environment, Chinese Academy of Sciences, Xiamen 361021 (China); State Key Laboratory of Environmental Sciences, and Key Laboratory of Ministry of Education for Coast and Wetland Ecosystems, School of Life Sciences, Xiamen University, Xiamen 361005 (China); Zheng, Tianling [State Key Laboratory of Environmental Sciences, and Key Laboratory of Ministry of Education for Coast and Wetland Ecosystems, School of Life Sciences, Xiamen University, Xiamen 361005 (China); Yu, Xin, E-mail: xyu@iue.ac.cn [Key Laboratory of Urban Environment and Health, Institute of Urban Environment, Chinese Academy of Sciences, Xiamen 361021 (China)

    2013-10-01

    The disinfection process for inactivating microorganisms at drinking water treatment plants is aimed for safety of drinking water for humans from a microorganism, such as bacteria, viruses, algae, fungi by using chlorination, ozonation, UV irradiation, etc. In the present study, a combination of two disinfectants, UV irradiation followed by chlorination, was evaluated for inactivating Aspergillus flavus under low contact time and low dosage of UV irradiation. The results indicated an inverse correlation between the inactivation of A. flavus by using UV irradiation only or chlorination alone. By using UV radiation, the 2 log{sub 10} control of A. flavus was achieved after 30 s of irradiation, while chlorination was observed to be more effective than UV, where the 2 log was achieved at chlorine concentration of 0.5, 1, 2 and 3 mg/l, in contact time of 60, 5, 1 and 1 min, respectively. However, combined use (UV irradiation followed by chlorination) was more effective than using either UV or chlorination alone; 5 s UV irradiation followed by chlorination produced 4 log{sub 10} reduction of A. flavus at chlorine concentrations of 2 and 3 mg/l under a contact time of 15 min. The results indicated that efficiency of UV irradiation improves when followed by chlorination at low concentrations. - Highlights: • As a disinfectant, chlorine is more effective than UV in inactivating Aspergillus flavus. • As a combined method, UV irradiation followed by chlorination shows high efficiency. • UV irradiation can improve effectiveness of chlorination in reducing Aspergillus flavus.

  6. Halopyrroles: a new group of highly toxic disinfection byproducts formed in chlorinated saline wastewater.

    Science.gov (United States)

    Yang, Mengting; Zhang, Xiangru

    2014-10-21

    Utilizing seawater for toilet flushing is an effective way to conserve freshwater in coastal cities. During chlorination for disinfecting saline wastewater effluents, the high levels of bromide from seawater are oxidized to hypobromous acid which may then react with effluent organics to form brominated disinfection byproducts (DBPs). In this research, by applying a new precursor ion scan method, we detected and identified a group of halopyrroles in a chlorinated saline wastewater effluent, including tetrabromopyrrole, tribromochloropyrrole, tribromoiodopyrrole, and tribromopyrrole, with tetrabromopyrrole as the predominant species. It is the first time that this group of halopyrroles were identified as wastewater DBPs (though 2,3,5-tribromopyrrole has been found to be a DBP in drinking water before). Detection of halopyrroles was problematic as these compounds in the pretreated samples were found to convert to halonitropyrroles; the problem was successfully solved by diluting the pretreated samples. The formation, occurrence, precursor, and toxicity of tetrabromopyrrole were investigated. This DBP showed significantly higher developmental toxicity than any of the haloaliphatic and haloaromatic DBPs previously tested. PMID:25236171

  7. The geochemistry of stable chlorine and bromine isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Eggenkamp, Hans [Onderzock and Beleving, Bussum (Netherlands)

    2014-11-01

    First book solely dedicated to the geochemistry of chlorine and bromine isotopes. Detailed description of analytical techniques, including their advantages and disadvantages. Indication of research fields where measurement of these isotopes is especially useful. This book provides detailed information on the history, analysis and applications of chlorine and bromine isotope geochemistry. Chlorine and bromine are geochemically unique as they prefer to exist as single charged negative ions. For this reason isotope fractionation reflects mostly processes that are not related to changes in the redox state and this fractionation is generally modest. The book will describe the processes that are most easily detected using these isotopes. Also isotope variations, and processes that cause them, measured in oxidised species such as perchlorates and in organic molecules will be described in this book.

  8. Papillomas on fish exposed to chlorinated wastewater effluent.

    Science.gov (United States)

    Grizzle, J M; Melius, P; Strength, D R

    1984-11-01

    The presence of carcinogenic and mutagenic chemical(s) in the effluent of a wastewater treatment plant was indicated by papillomas developing on caged black bullheads (Ictalurus melas), hepatic enzyme induction in exposed fish, and Ames test mutagenicity of organic extracts of the wastewater. Although virus-like particles have been reported in papillomas of several other fish species, no evidence was obtained for the presence of viruses in the black bullhead papillomas. Mutagenic and carcinogenic chemicals were not identified in the wastewater, but chlorination was implicated as a factor contributing to the induction of the papillomas. The prevalence of papillomas on wild black bullheads exposed to the effluent decreased from 73 to 23% after the amount of residual chlorine (CAS: 7782-50-5) in the effluent leaving the chlorine contact chamber was reduced from 1.3-3.1 mg/liter to 0.25-1.2 mg/liter. PMID:6593489

  9. Electronic diffraction study of the chlorination of nickel

    International Nuclear Information System (INIS)

    A study has been made of the chlorination of the (100), (110) and (111) crystal faces of nickel using high energy electron diffraction and electron microscopy. Two methods have been used: bombardment with chlorine ions having an energy of between 10 and 30 keV, and direct chlorination in a diffractor at pressures of about 10-4 torr. It has thus been possible to show the very special properties of nickel chloride (CdBr2 type, space group R 3-bar m) which is always formed along the (0001) plane, whatever the orientation of the substrate. It has also been possible to attain the metal-halide interface and to show the existence of two-dimensional chemisorbed films which are ordered or disordered according to the crystal orientation. (author)

  10. Chlorination of Carbon Nanotubes Obtained on the Different Metal Catalysts

    Directory of Open Access Journals (Sweden)

    Iwona Pełech

    2013-01-01

    Full Text Available In this paper, a chlorination method is proposed for simultaneous purification and functionalization of carbon nanotubes, thus increasing their ability to use. Carbon nanotubes were obtained by CVD method through ethylene decomposition on the nanocrystalline iron or cobalt or bimetallic iron-cobalt catalysts. The effects of temperature (50, 250, and 450°C in the case of carbon nanotubes obtained on the Fe-Co catalyst and type of catalyst (Fe, Co, Fe/Co on the effectiveness of the treatment and functionalization were tested. The phase composition of the samples was determined using the X-ray diffraction method. The quantitative analysis of metal impurity content was validated by means of the thermogravimetric analysis. Using X-ray Photoelectron Spectroscopy (XPS, Energy Dispersive Spectroscopy (EDS analysis, and also Mohr titration method, the presence of chlorine species on the surface of chlorinated samples was confirmed.

  11. Transformation of phenazone-type drugs during chlorination.

    Science.gov (United States)

    Rodil, Rosario; Quintana, José Benito; Cela, Rafael

    2012-05-01

    Chlorination is one of the most popular disinfection steps for water treatment in Europe. However, chlorine can react with pharmaceuticals and other micropollutants leading to either their elimination or by-products being formed. These by-products are frequently not identified and therefore the consequences of chlorination can be underestimated. In this work, the degradation of two analgesics and antipyretics, phenazone (antipyrine) and propyphenazone, during chlorination was investigated by liquid chromatography-mass spectrometry (LC-MS). A quadrupole-time-of-flight (Q-TOF) system was used to follow the time course of the pharmaceuticals, and also used in the identification of the by-products. The degradation kinetics was investigated at different concentrations of chlorine (1-10 mg/L), bromide (0-100 μg/L) and sample pH (5.7-8.3) by means of a Box-Behnken experimental design. Depending on these factors, half-lives were in the ranges: 0.9-295 s for phenazone and 0.4-173 s for propyphenazone. Also, it was observed that chlorine concentration was a significant factor for propyphenazone, resulting in increased degradation rate as it is increased. The transformation path of these drugs consisted mainly of halogenations, hydroxylations and dealkylations. After several days of reaction two derivatives remained stable for phenazone: chloro-hydroxy-phenazone and N-demethyl-chloro-hydroxy-phenazone and two for propyphenazone: N-demethyl-hydroxy-propyphenazone and N-demethyl-chloro-hydroxy-propyphenazone. Moreover, experiments conducted with real water matrices, tap and surface water, showed that reaction, and formation of by-products, can take place both at the emission source point (household) and during drinking water production. PMID:22381982

  12. On chlorization of uranium and plutonium oxides in NaCl-KCl-MgCl2 molten eutectic

    International Nuclear Information System (INIS)

    The chlorination process of U3O8, UO2, and PuO2 in a melt of anhydrous NaCl-KCl-MgCl2 with gaseous chlorine and carbon tetrachloride has been studied. The chlorination rate of uranium oxides has been studied within a temperature range 500-800 deg C at a chlorine feeding rate of 10 ml/min. Thermoqravimetric and X-ray analyses have shown that K2UO2Cl4 compound is the final product of chlorination of uranium oxides. The mechanism of chlorination has been proposed. THe rate of PuO2 chlorination has been studied within the same temperature range. It has been established that PuO2 is readily chlorinated with CCl4 vapours at a feeding rate of 10 ml/min. In contrast to uranium, chloride forms of plutonium in a highest oxidized state are unstable and are reduced in the melt to Pu(3) and Pu(4). The oxygen being released is retained by CCl4 and by the products of CCl4 pyrolysis

  13. Method for combined removal of mercury and nitrogen oxides from off-gas streams

    Science.gov (United States)

    Mendelsohn, Marshall H.; Livengood, C. David

    2006-10-10

    A method for removing elemental Hg and nitric oxide simultaneously from a gas stream is provided whereby the gas stream is reacted with gaseous chlorinated compound to convert the elemental mercury to soluble mercury compounds and the nitric oxide to nitrogen dioxide. The method works to remove either mercury or nitrogen oxide in the absence or presence of each other.

  14. 76 FR 62149 - American Chemistry Council, The Chlorine Institute, Inc., the Fertilizer Institute, and PPG...

    Science.gov (United States)

    2011-10-06

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF TRANSPORTATION Surface Transportation Board American Chemistry Council, The Chlorine Institute, Inc., the Fertilizer... American Chemistry Council, The Chlorine Institute, Inc., The Fertilizer Institute (TFI), and...

  15. Supplying sodium and chlorine is effective on patients with congestive heart failure

    Institute of Scientific and Technical Information of China (English)

    Yu Li; Changcong Cui

    2005-01-01

    Objective: To analyze the relationship of severity of heart failure and the concentration of serum sodium(Na + ) and chlorine(Cl- ) and to explore the effect of supplying sodium and chlorine on patients with Congestive heart failure. Methods: 80 patients with congestive heart failure were divided into two groups, namely supplying and control group. Serum sodium and chlorine were measured in all these patients. All treatments but supplying sodium and chlorine were same between the supplying and control groups. Results:According to NYHA, patients who were in class Ⅳ had lower level of serum sodium and chlorine than those in class Ⅱ ( P < 0.05). The heart function was improved after the level of serum sodium and chlorine were raised. Conclusions: The concentration of serum sodium and chlorine relates to the severity of heart failure. The therapy of supplying sodium and chlorine is an effective way to decrease death rate.

  16. Project Summary. IN-SITU AQUIFER RESTORATION OF CHLORINATED ALIPHATICS BY METHANOTROPHIC BACTERIA

    Science.gov (United States)

    This project evaluated the potential of an innovative approach to aquifer restoration: enhanced in-situ biotransformation of chlorinated aliphatic solvents by a bacterial community grown on methane under aerobic conditions. The target chlorinated compounds were trichloroethene (...

  17. The Health Effects of Chlorine Dioxide as a Disinfectant in Potable Water: A Literature Survey

    Science.gov (United States)

    Calabrese, Edward J.; And Others

    1978-01-01

    The use of chlorine dioxide as a disinfectant in water is being considered by the EPA. This article presents a summary of the known published reports concerning health effects of chlorine dioxide on animal and human populations. (Author/MA)

  18. Chlorine release from biomass. Part 6; Kloravgaang fraan biobraenslen. Del 6

    Energy Technology Data Exchange (ETDEWEB)

    Zintl, Frank; Stroemberg, Birgitta [TPS Termiska Processer AB, Nykoeping (Sweden)

    2000-04-01

    Chlorine release from model compounds and different biomass fuels has been studied during thermal treatment in an electric oven in inert atmosphere (N{sub 2}) and with addition of 10% O{sub 2}. The amount of chlorine in all investigated materials has been kept to 2% with addition of KCl solution in methanol. The amount of chlorine was analysed before and after treatment in the decided atmosphere and to the temperature chosen. The influence from different functional groups on the chlorine release at low temperatures has been studied in pyrolysis experiments of simple model compounds with different structures. A good correlation between the chlorine release and the functional groups in the model substances was achieved. Results from the experiments shows that the early chlorine release, is most likely to occur in all biofuels, since all biomass fuels contains biological material with significant amounts of functional groups which can interact with fuel chlorine ( inorganic chlorine)

  19. Effects of ozone and ozone/peroxide pretreatments on disinfection byproduct formation during subsequent chlorination and chloramination.

    Science.gov (United States)

    Yang, Xin; Peng, Jinfeng; Chen, Baiyang; Guo, Wanhong; Liang, Yongmei; Liu, Wei; Liu, Lu

    2012-11-15

    Ozone (O3) and ozone/hydrogen peroxide (O3/H2O2) can be used in water treatment facilities to remove many organic micropollutants with taste, odor, and color implications. The effects of O3 and O3/H2O2 on the formation of disinfection byproducts (DBPs) in subsequent chlorination and chloramination processes, however, are not well determined. In this study, we compared the yields of a series of regulated and emerging DBPs during sequenced O3-Cl2, O3/H2O2-Cl2, O3-NH2Cl, and O3/H2O2-NH2Cl oxidation of 11 samples, each with different hydrophobicity, bromide concentration, soluble microbial products, and humic substances. For most water, pretreatment with O3 and O3/H2O2 increased the formation of chloral hydrate (CH), trichloronitromethane (TCNM) and haloketones (HKs) but lowered the yields of haloacetonitriles (HANs) during chlorination processes. Compared with O3 alone, O3/H2O2 in combination generated more CH and HKs during chlorination, and their extents of formation appeared to depend on the O3 doses. In terms of chloramination, both O3 and O3/H2O2 reduced THM, HAA, and HAN formation significantly without increasing CH, TCNM, or HKs. These results suggest that O3 or O3/H2O2 pretreatments may provide some benefits for the chloramination process in controlling regulated and emerging DBPs in waters without high bromide content. PMID:23009791

  20. Proportion of bromo-DBPs in total DBPs during reclaimed-water chlorination and its related influencing factors

    Institute of Scientific and Technical Information of China (English)

    ZHANG Hua; QU JiuHui; LIU HuiJuan; ZHAO Xu

    2008-01-01

    During the chlorine disinfection of reclaimed-water, the proportion of bromo-disinfection by-products (bromo-DBPs) in total DBPs is affected by chlorine dosage, reaction time, Ph, ammonia nitrogen (NH3-N) and preozonation. Results show that bromo-trihalomethanes (bromo-THMs) form more easily than bromo-haloacetic acids (bromo-HAAs) and bromine incorporation in DBPs decreases with the increase of chlorine dosage. Within 5 h, bromine incorporation in THMs (n(Br)) increases but bromine incorporation in HAAs (n'(Br)) decreases with the extension of reaction time; however, n(Br) decreases and n'(Br) keeps relatively constant at a longer reaction time. Furthermore, bromine incorporation in DBPs is low under acidic and alkaline conditions. The increase of NH3-N concentration inhibits the formation of chloro-DBPs, resulting in the increase of n(Br) and n'(Br) to some extent. Preozonation enhances the formation of HOBr and the increase of bromine incorporation in DBPs; however, ozone of a high concentration oxidizes HOBr to its salt form, leading to the decrease of bromine incorporation in DBPs.

  1. Proportion of bromo-DBPs in total DBPs during reclaimed-water chlorination and its related influencing factors

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    During the chlorine disinfection of reclaimed-water, the proportion of bromo-disinfection by-products (bromo-DBPs) in total DBPs is affected by chlorine dosage, reaction time, pH, ammonia nitrogen (NH3-N) and preozonation. Results show that bromo-trihalomethanes (bromo-THMs) form more easily than bromo-haloacetic acids (bromo-HAAs) and bromine incorporation in DBPs decreases with the increase of chlorine dosage. Within 5 h, bromine incorporation in THMs (n(Br)) increases but bromine incorpo-ration in HAAs (n′(Br)) decreases with the extension of reaction time; however, n(Br) decreases and n′(Br) keeps relatively constant at a longer reaction time. Furthermore, bromine incorporation in DBPs is low under acidic and alkaline conditions. The increase of NH3-N concentration inhibits the formation of chloro-DBPs, resulting in the increase of n(Br) and n′(Br) to some extent. Preozonation enhances the formation of HOBr and the increase of bromine incorporation in DBPs; however, ozone of a high con-centration oxidizes HOBr to its salt form, leading to the decrease of bromine incorporation in DBPs.

  2. Thermodynamic equilibrium diagram of the chlorine-titanium system

    Institute of Scientific and Technical Information of China (English)

    DU Ailing; GUO Xiaofei; ZHANG Heming; LIU Jiang

    2005-01-01

    The chemical and electrochemical equilibria of the chlorine-titanium system in the presence of gaseous phase were investigated. Many species, which consisted of chlorine and titanium, were considered. Various thermodynamic equilibria were calculated in the different pressures at different temperatures. The calculated results were shown as log p-1/T and E-T diagrams. These diagrams may be used as important tools for corrosion study and titanium production. The diagrams are also used to thermodynamically determine the existence areas of various species and so on.

  3. Inactivation of human and simian rotaviruses by chlorine dioxide.

    OpenAIRE

    Chen, Y.S.(China Institute of Atomic Energy, P.O. Box 275 (10), Beijing 102413, PR China); Vaughn, J M

    1990-01-01

    The inactivation of single-particle stocks of human (type 2, Wa) and simian (SA-11) rotaviruses by chlorine dioxide was investigated. Experiments were conducted at 4 degrees C in a standard phosphate-carbonate buffer. Both virus types were rapidly inactivated, within 20 s under alkaline conditions, when chlorine dioxide concentrations ranging from 0.05 to 0.2 mg/liter were used. Similar reductions of 10(5)-fold in infectivity required additional exposure time of 120 s at 0.2 mg/liter for Wa a...

  4. The chlorine isotope fingerprint of the lunar magma ocean

    OpenAIRE

    Boyce, Jeremy W.; Treiman, Allan H.; Guan, Yunbin; Ma, Chi; Eiler, John M.; Gross, Juliane; Greenwood, James P.; Stolper, Edward M.

    2015-01-01

    The Moon contains chlorine that is isotopically unlike that of any other body yet studied in the Solar System, an observation that has been interpreted to support traditional models of the formation of a nominally hydrogen-free (“dry”) Moon. We have analyzed abundances and isotopic compositions of Cl and H in lunar mare basalts, and find little evidence that anhydrous lava outgassing was important in generating chlorine isotope anomalies, because ^(37)Cl/^(35)Cl ratios are not related to Cl a...

  5. Sonochemical Treatment of Water Polluted by Chlorinated Organocompounds. A Review

    Directory of Open Access Journals (Sweden)

    Olivier Louisnard

    2010-02-01

    Full Text Available As one of several types of pollutants in water, chlorinated compounds have been routinely subjected to sonochemical analysis to check the environmental applications of this technology. In this review, an extensive study of the influence of the initial concentration, ultrasonic intensity and frequency on the kinetics, degradation efficiency and mechanism has been analyzed. The sonochemical degradation follows a radical mechanism which yields a very wide range of chlorinated compounds in very low concentrations. Special attention has been paid to the mass balance comparing the results from several analytical techniques. As a conclusion, sonochemical degradation alone is not an efficient treatment to reduce the organic pollutant level in waste water.

  6. Chlorination of commercial molybdenite concentrate in a fluidized bed reactor

    Science.gov (United States)

    Nair, K. U.; Sathiyamoorthy, D.; Bose, D. K.; Sundaresan, M.; Gupta, C. K.

    1987-06-01

    Studies on recovery of molybdenum from commercial grade molybdenite using the technique of fluidized bed chlorination in the presence of oxygen are presented. Molybdenum recovery above 99 pct at a chlorine utilization efficiency of 84 pct has been achieved for a fluidizing gas flow-rate of 3 L/min of the gases Cl2, O2, and N2 mixed in the proportion of 2∶5∶23, respectively, at 300 °C. The investigations on kinetics showed that the overall oxychlorination reaction is controlled by chemical reaction and is of first order with respect to particle surface area.

  7. Chlorine international thermodynamic tables of the fluid state

    CERN Document Server

    Angus, S; de Reuck, K M

    1985-01-01

    Chlorine: International Thermodynamic Tables of the Fluid State-8 is a four-chapter book that covers available and estimated data on chlorine; estimation of the element's properties; the correlating equations for the element; and how the tabulated properties are calculated from chosen equation. The tables in this book give the volume, entropy, enthalpy, isobaric heat capacity, compression factor, fugacity/pressure ratio, Joule-Thomson coefficient, ratio of the heat capacities, and speed of sound as a function of pressure and temperature. Given in the tables as well are the pressure, entropy, i

  8. Enhanced reductive dechlorination in clay till contaminated with chlorinated solvents

    DEFF Research Database (Denmark)

    Damgaard, Ida

    Chlorinated solvents are among the most frequently found contaminants in groundwater. In fractured media, chlorinated ethenes and ethanes are transported downwards through preferential pathways with subsequent diffusion into the sediment matrix. Due to slow back diffusion it can serve as a long...... the potential for development of degradation throughout the entire clay matrix. When ERD is applied in a low permeability settings one of the major constraints is to obtain the necessary contact between electron donor, bacteria and contaminants to achieve reasonable remediation timeframes. Two injection methods...

  9. Dechlorination by combined electrochemical reduction and oxidation*

    OpenAIRE

    Cong, Yan-qing; Wu, Zu-cheng; Tan, Tian-en

    2005-01-01

    Chlorophenols are typical priority pollutants listed by USEPA (U.S. Environmental Protection Agency). The removal of chlorophenol could be carried out by a combination of electrochemical reduction and oxidation method. Results showed that it was feasible to degrade contaminants containing chlorine atoms by electrochemical reduction to form phenol, which was further degraded on the anode by electrochemical oxidation. Chlorophenol removal rate was more than 90% by the combined electrochemical r...

  10. Chlorine Dioxide Inactivation of Cryptosporidium parvum Oocysts and Bacterial Spore Indicators

    OpenAIRE

    Chauret, Christian P.; Radziminski, Chris Z.; Lepuil, Michael; Creason, Robin; Andrews, Robert C.

    2001-01-01

    Cryptosporidium parvum, which is resistant to chlorine concentrations typically used in water treatment, is recognized as a significant waterborne pathogen. Recent studies have demonstrated that chlorine dioxide is a more efficient disinfectant than free chlorine against Cryptosporidium oocysts. It is not known, however, if oocysts from different suppliers are equally sensitive to chlorine dioxide. This study used both a most-probable-number–cell culture infectivity assay and in vitro excysta...

  11. Combustion Characteristics of Chlorine-Free Solid Fuel Produced from Municipal Solid Waste by Hydrothermal Processing

    OpenAIRE

    Kunio Yoshikawa; Pandji Prawisudha; Bayu Indrawan

    2012-01-01

    An experimental study on converting municipal solid waste (MSW) into chlorine-free solid fuel using a combination of hydrothermal processing and water-washing has been performed. After the product was extracted from the reactor, water-washing experiments were then conducted to obtain chlorine-free products with less than 3000 ppm total chlorine content. A series of combustion experiments were then performed for the products before and after the washing process to determine the chlorine conten...

  12. Killing Chlorella with chlorine dioxide%二氧化氯杀灭小球藻

    Institute of Scientific and Technical Information of China (English)

    李绍秀; 夏文琴; 赵德骏; 袁秀丽; 王志红; 李冬梅; 谢葆红

    2012-01-01

    The experiments of the effect of the ClO2 dosage,initial algal concentration,pH,organic matter and ammonia nitrogen concentration on killing Chlorella in water from reservoir with chlorine dioxide were carried out.The Chlorella removal effect by combining chlorine dioxide oxidation with coagulation was investigated,and the process conditions were optimized.The results showed that the efficiency of killing Chlorella was 71.93% after 10 minutes when chlorine dioxide dosage was 1.1 mg/L.The efficiency of killing Chlorella rose with the increase of chlorine dioxide dosage and initial algal concentration,but decreased remarkably with the increase of organic matter concentration.Ammonia nitrogen had little effect on killing Chlorella.In acidity and basicity conditions,the efficiency of killing Chlorella sharp declined with the increase of pH,but descended slowly from neutral to weak base.For the raw water from reservoir which Chlorella was the advantage alga,the removal efficiency of algae was 98.47% when chlorine dioxide oxidation was combined with coagulation.The best process conditions were that the dosages of ClO2 and aluminium polychlorid were 0.5 mg/L and 5 mg/L,respectively,adding ClO2 and PAC simultaneously.%实验研究了二氧化氯投加量、小球藻的初始浓度、pH、有机物和氨氮含量对ClO2杀灭来自于水库水的小球藻的影响,考察了ClO2氧化与混凝工艺结合时去除小球藻的效果并对工艺条件进行优化。结果表明,ClO2在投加量1.1 mg/L下,接触10 min,小球藻的杀灭率为71.93%。小球藻的杀灭率随着ClO2投加量的增大和藻初始浓度的升高而提高,随水中有机物含量的增加而显著降低,氨氮含量对小球藻杀灭的效果影响很小。在酸性条件和碱性条件下,小球藻的杀灭率均随pH升高而急剧下降,而在中性至弱碱性区间内,藻的杀灭率随pH升高而缓慢下降。对于某以小球藻为优势藻的供水水库源水,ClO2氧化与混凝工

  13. COLORIMETRIC ASSAY OF CHLORINE IN SOIL%土壤中氯的比色测定

    Institute of Scientific and Technical Information of China (English)

    聂全新; 陶文靖; 胡兰

    2014-01-01

    本法采用碳酸钠-氧化锌混合试剂半熔后硫氰酸汞比色测定了土壤中微量的氯。实验并确定了各试剂的最佳加入量,方法相对标准偏差(RSD,n=12)为2%~9%。经国家标准物质验证,测定值与认定值基本符合。%This method is to measure trace chlorine in soil by mercury thiocyanate colorimetry using half-melted mixture of sodium carbonate and zinc oxide. It tested and determined the best addition of each reagent with RSD of 2%~9%. Checked by national standard reference material, the measurement fits certified value in general.

  14. Potential of non-ligninolytic fungi in bioremediation of chlorinated and polycyclic aromatic hydrocarbons.

    Science.gov (United States)

    Marco-Urrea, Ernest; García-Romera, Inmaculada; Aranda, Elisabet

    2015-12-25

    In previous decades, white-rot fungi as bioremediation agents have been the subjects of scientific research due to the potential use of their unspecific oxidative enzymes. However, some non-white-rot fungi, mainly belonging to the Ascomycota and Zygomycota phylum, have demonstrated their potential in the enzymatic transformation of environmental pollutants, thus overcoming some of the limitations observed in white-rot fungi with respect to growth in neutral pH, resistance to adverse conditions and the capacity to surpass autochthonous microorganisms. Despite their presence in so many soil and water environments, little information exists on the enzymatic mechanisms and degradation pathways involved in the transformation of hydrocarbons by these fungi. This review describes the bioremediation potential of non-ligninolytic fungi with respect to chlorinated hydrocarbons and polycyclic aromatic hydrocarbons (PAHs) and also shows known conversion pathways and the prospects for future research.

  15. Interactions of N,N'-dimethylaminoethanol with steel surfaces in alkaline and chlorine containing solutions

    Science.gov (United States)

    Welle, A.; Liao, J. D.; Kaiser, K.; Grunze, M.; Mäder, U.; Blank, N.

    1997-10-01

    Formulations based on dilute aqueous solutions of N,N'-dimethylethanolamine (DMEA) are used to protect reinforcement steel bars ('rebar') in concrete from corrosion. In a previous paper we discussed the usefulness of X-ray photoelectron spectroscopy (XPS) to detect DMEA adsorbed from solution and the application of secondary neutral mass spectrometry (SNMS) to study migration of DMEA through a cement matrix. In this report we present XPS data of DMEA adsorbed on steel surfaces from alkaline and chlorine containing solutions of variable concentration range and discuss models for the interaction of DMEA with the oxidized steel surface and the mechanism of corrosion inhibition of DMEA. DMEA is strongly bonded to the steel surface and displaces ionic species from the substrate/solution interface hence protecting the ironoxide surface from ionic attack.

  16. Recovery of Niobium and Zirconium from the Cyclone Discharge of Chlorination Plant Producing Titanium Tetrachloride

    Directory of Open Access Journals (Sweden)

    V. S. Gireesh

    2014-03-01

    Full Text Available This paper describes a method for recovering niobium and zirconium from the cyclone solid residues arising from chlorination of titaniferrous ores. The residue contains beneficiated ilmenite (BI fines, calcined petroleum coke (CPC and metal chlorides of niobium, aluminium, zirconium, iron, manganese, vanadium etc. The BI fines and CPC present in the residue were removed by soaking the residue with water and by separating the insoluble fraction contain BI and CPC by filtration. The filtrate containing the soluble metal chlorides was acidified with hydrochloric acid followed by agitation and heating in the presence of sulphate ions (sulphuric acid to precipitate niobium and zirconium as their oxo sulphate which is filtered, dried and calcined to convert niobium and zirconium oxides. The optimum amount of sulphuric acid was found to be 3 % and the optimum pH and temperature for precipitation of niobium and zirconium is 0.5 and 90 oC respectively.

  17. Chlorine gas sensing performance of palladium doped nickel ferrite thin films

    Science.gov (United States)

    Rao, Pratibha; Godbole, R. V.; Bhagwat, Sunita

    2016-05-01

    NiFe2O4 and Pd:NiFe2O4 (Pd=1 w/o, 3 w/o and 5 w/o) thin films, p-type semiconducting oxides with an inverse spinel structure have been used as a gas sensor to detect chlorine. These films were prepared by spray pyrolysis technique and XRD was used to confirm the structure. The surface morphology was studied using SEM. Magnetization measurements were carried out at room temperature using SQUID VSM, which shows ferrimagnetic behavior of the samples. The reduction in optimum operating temperature and enhancement in response was observed on Pd-incorporation in nickel ferrite thin films. Faster response and recovery characteristic is observed Pd-incorporated nickel ferrite thin films. The long-term stability is evaluated over a period of six months. This feature may be regarded as a significant facet towards their practical application as gas sensors.

  18. Chlorine cell disinfection determination with flow cell cytometry and plate count (poster)

    NARCIS (Netherlands)

    Peters, M.C.F.M.; Keuten, M.G.A.; De Kreuk, M.K.; Van Loosdrecht, M.C.M.; Rietveld, L.C.

    2013-01-01

    Chlorine is used for disinfection in different water systems. This research focuses on chlorine disinfection in swimming pool water. In the Netherlands, free available chlorine concentrations in swimming pools are limited between 0.5-1.5 mg/L, which is based on a 4-log removal of Pseudomonas aerugin

  19. Evaluating potential chlorinated methanes degradation mechanisms and treatments in interception trenches filled with concrete-based construction wastes

    Science.gov (United States)

    Rodríguez-Fernandez, Diana; Torrentó, Clara; Rosell, Mònica; Audí-Miró, Carme; Soler, Albert

    2014-05-01

    conditions in the trenches with in situ chemical oxidation (ISCO), which would be able to remove the rest of the accompanying pollutants, is proposed and merits evaluation. Preliminary batch experiments were performed to evaluate the feasibility of different chemical oxidation reactions (permanganate, persulphate, hydrogen peroxide and Fenton) on the complex contaminated recharge water which were, in general, more effective for degrading the chlorinated ethenes than for the chlorinated methanes (Torrentó et al. EGU 2012). Therefore, this study seeks to improve the understanding of CF and CT degradation mechanisms/processes that are going on in the interception trenches as well as to select between the two most effective chemical oxidation remediation treatments (persulphate and permanganate) taking into account their efficiency respect the chlorinated methanes removal, the generated acute toxicity and the applicability of the carbon isotopic fractionation as an indicator of the effectiveness of the future in situ remediation. Additionally, ongoing batch experiments are expected to elucidate if CT is undergoing abiotic reductive dechlorination by Fe-bearing minerals such as hydrophobic green rust (Ayala-Luis et al., 2012) which transform CT into non-chlorinated substances such as formic acid and carbon monoxide. This unstable iron compound might be formed in the interception trenches during chloride induced corrosion of iron mineral phases present in the concrete-based construction wastes (Sagoe-Crentsil and Glasser, 1993). The role of other minerals like iron oxy-hydroxides, carbonates or sulphides cannot be discarded at all. The potential of δ13C values to assess the efficiency of this abiotic CT degradation reaction will be also evaluated. References Ayala-Luis, K.; Cooper, N.; Bender C. and Hansen. H. (2012) Efficient dechlorination of carbon tetrachloride by hydrophobic green rust intercaled with dodecanoate anions. Environmental Science & Technology 46, 3390

  20. Chlorine-36 and the initial value problem

    Science.gov (United States)

    Davis, Stanley N.; Cecil, DeWayne; Zreda, Marek; Sharma, Pankaj

    Chlorine-36 is a radionuclide with a half-life of 3.01×105a. Most 36Cl in the hydrosphere originates from cosmic radiation interacting with atmospheric gases. Large amounts were also produced by testing thermonuclear devices during 1952-58. Because the monovalent anion, chloride, is the most common form of chlorine found in the hydrosphere and because it is extremely mobile in aqueous systems, analyses of both total Cl- as well as 36Cl have been important in numerous hydrologic studies. In almost all applications of 36Cl, a knowledge of the initial, or pre-anthropogenic, levels of 36Cl is useful, as well as essential in some cases. Standard approaches to the determination of initial values have been to: (a) calculate the theoretical cosmogenic production and fallout, which varies according to latitude; (b) measure 36Cl in present-day precipitation and assume that anthropogenic components can be neglected; (c) assume that shallow groundwater retains a record of the initial concentration; (d) extract 36Cl from vertical depth profiles in desert soils; (e) recover 36Cl from cores of glacial ice; and (f) calculate subsurface production of 36Cl for water that has been isolated from the atmosphere for more than one million years. The initial value from soil profiles and ice cores is taken as the value that occurs directly below the depth of the easily defined bomb peak. All six methods have serious weaknesses. Complicating factors include 36Cl concentrations not related to cosmogenic sources, changes in cosmogenic production with time, mixed sources of chloride in groundwater, melting and refreezing of water in glaciers, and seasonal groundwater recharge that does not contain average year-long concentrations of 36Cl. Résumé Le chlore-36 est un radionucléide de période 3.01×105a. Pour l'essentiel, le 36Cl dans l'hydrosphère provient des effets du rayonnement cosmique sur les gaz atmosphériques. De grandes quantités de 36Cl ont aussi été produites au cours des

  1. Reactivity of chlorine radical with submicron palmitic acid particles: kinetic measurements and products identification

    Directory of Open Access Journals (Sweden)

    M. Mendez

    2013-06-01

    Full Text Available The heterogeneous reaction of Cl. radicals with sub-micron palmitic acid (PA particles was studied in an aerosol flow tube in the presence or in the absence of O2. Fine particles were generated by homogeneous condensation of PA vapors and introduced in the reactor where chlorine atoms are produced by photolysis of Cl2 using UV lamps surrounding the reactor. The effective reactive uptake coefficient (γ has been determined from the rate loss of PA measured by GC/MS analysis of reacted particles as a function of the chlorine exposure. In the absence of O2, γ = 14 ± 5 indicates efficient secondary chemistry involving Cl2. GC/MS analyses have shown the formation of monochlorinated and polychlorinated compounds in the oxidized particles. Although, the PA particles are solid, the complete mass can be consumed. In the presence of oxygen, the reaction is still dominated by secondary chemistry but the propagation chain length is smaller than in the absence of O2 which leads to an uptake coefficient γ = 3 ± 1. In the particulate phase, oxocarboxylic acids and dicarboxylic acids are identified by GC/MS. Formation of alcohols and monocarboxylic acids are also suspected. All these results show that solid organic particles could be efficiently oxidized by gas-phase radicals not only on their surface, but also in bulk by mechanisms which are still unclear. Furthermore the identified reaction products are explained by a chemical mechanism showing the pathway of the formation of more functionalized products. They help to understand the aging of primary tropospheric aerosol containing fatty acids.

  2. Reactions of oxidation of plutonium metal

    International Nuclear Information System (INIS)

    The investigation into preparation of the powdery plutonium oxides under the reaction of metal plutonium with moist (5 % H2O) air and moist (5 % H2O) argon was carried out. The kinetic dependences in the 250 - 400 Deg C range are demonstrated. The vicissitude of the oxidation is shown, the activation energy is calculated for every stage. The mechanism of the metal plutonium oxidation is proposed. The obtained plutonium oxides were shown to have a high reaction ability at 300 - 400 Deg C in the moist air and moist argon media, and to be feasible for the further chemical treatment - dissolving in nitric acid, fluorination and chlorination

  3. Effect of sulfur dioxide on indium(3) sulfate chlorination

    International Nuclear Information System (INIS)

    The results of thermodynamic calculations and kinetic investigations of In2(SO4)3 interaction with gaseous Cl2 and equimolar Cl2 and SO2 mixture at 127-800 deg C are presented. It is found that acceleration of chlorination rate takes place in the presence of SO2, while the temperature of its beginning and activation energy decrease

  4. In situ aerobic cometabolism of chlorinated solvents: a review.

    Science.gov (United States)

    Frascari, Dario; Zanaroli, Giulio; Danko, Anthony S

    2015-01-01

    The possible approaches for in situ aerobic cometabolism of aquifers and vadose zones contaminated by chlorinated solvents are critically evaluated. Bioaugmentation of resting-cells previously grown in a fermenter and in-well addition of oxygen and growth substrate appear to be the most promising approaches for aquifer bioremediation. Other solutions involving the sparging of air lead to satisfactory pollutant removals, but must be integrated by the extraction and subsequent treatment of vapors to avoid the dispersion of volatile chlorinated solvents in the atmosphere. Cometabolic bioventing is the only possible approach for the aerobic cometabolic bioremediation of the vadose zone. The examined studies indicate that in situ aerobic cometabolism leads to the biodegradation of a wide range of chlorinated solvents within remediation times that vary between 1 and 17 months. Numerous studies include a simulation of the experimental field data. The modeling of the process attained a high reliability, and represents a crucial tool for the elaboration of field data obtained in pilot tests and for the design of the full-scale systems. Further research is needed to attain higher concentrations of chlorinated solvent degrading microbes and more reliable cost estimates. Lastly, a procedure for the design of full-scale in situ aerobic cometabolic bioremediation processes is proposed. PMID:25306537

  5. The role of natural chlorinated hydroquinone metabolites in ligninolytic fungi

    NARCIS (Netherlands)

    Teunissen, P.J.M.

    1999-01-01

    Ligninolytic Basidiomycetes have been reported to produce a wide variety of chloroaromatic compounds as secondary metabolites, which are structurally similar to environmental pollutants. Among these are chlorinated hydroquinone metabolites (CHM), such as 2-chloro-1,4-dimethoxybenzene (2Cl-14DMB), 2,

  6. Bioremediation of chlorinated ethenes in aquifer thermal energy storage

    OpenAIRE

    Ni, Z

    2015-01-01

      Subjects: bioremediation; biodegradation; environmental biotechnology, subsurface and groundwater contamination; biological processes; geochemistry; microbiology The combination of enhanced natural attenuation (ENA) of chlorinated volatile organic compounds (CVOCs) and aquifer thermal energy storage (ATES) appears attractive because such integration provides a promising solution for redevelopment of urban areas in terms of improving the local environmental quality as well as achieving ...

  7. In situ aerobic cometabolism of chlorinated solvents: a review.

    Science.gov (United States)

    Frascari, Dario; Zanaroli, Giulio; Danko, Anthony S

    2015-01-01

    The possible approaches for in situ aerobic cometabolism of aquifers and vadose zones contaminated by chlorinated solvents are critically evaluated. Bioaugmentation of resting-cells previously grown in a fermenter and in-well addition of oxygen and growth substrate appear to be the most promising approaches for aquifer bioremediation. Other solutions involving the sparging of air lead to satisfactory pollutant removals, but must be integrated by the extraction and subsequent treatment of vapors to avoid the dispersion of volatile chlorinated solvents in the atmosphere. Cometabolic bioventing is the only possible approach for the aerobic cometabolic bioremediation of the vadose zone. The examined studies indicate that in situ aerobic cometabolism leads to the biodegradation of a wide range of chlorinated solvents within remediation times that vary between 1 and 17 months. Numerous studies include a simulation of the experimental field data. The modeling of the process attained a high reliability, and represents a crucial tool for the elaboration of field data obtained in pilot tests and for the design of the full-scale systems. Further research is needed to attain higher concentrations of chlorinated solvent degrading microbes and more reliable cost estimates. Lastly, a procedure for the design of full-scale in situ aerobic cometabolic bioremediation processes is proposed.

  8. ANALYSIS OF NASAL TISSUE FOR BIOMARKERS OF CHLORINE EXPOSURE

    Science.gov (United States)

    Both 3-chloro-tyrosine (CT) and 3,5-dichloro-tyrosine (dCT) are sensitive and specific biomarkers for evaluating exposure to chlorine gas (Cl2) and hypochlorous acid (HOCl). Previous investigations have focused on the formation of CT and dCT resulting from biochemical responses ...

  9. Transformation of chlorinated compounds by methanogenic granular sludge

    NARCIS (Netherlands)

    Eekert, van M.H.A.

    1999-01-01

    Chlorinated compounds are an important group of contaminants often found in sediments, groundwater, soils, wastewaters, and off-gasses. Many of these pollutants are found on the EPA list of Priority Pollutants indicating their potential hazard for the environment. Initial degradation can occur via d

  10. Degradation of Chlorinated Aromatic Compounds in UASB Reactors

    DEFF Research Database (Denmark)

    Christiansen, Nina; Hendriksen, Hanne Vang; Järvinen, Kimmo T.;

    1995-01-01

    Data on anaerobic degradation of chloroaromatic compounds in Upflow Anaerobic Sludge Blanket Reactors (UASB-reactor) are presented and compared. Special attention is given to the metabolic pathways for degradation of chlorinated phenols by granular sludge. Results indicate that PCP can be degraded...

  11. Transformation of Chlorinated Hydrocarbons on Synthetic Green Rusts

    Science.gov (United States)

    Green rusts (GRs) are layered double hydroxides that contain both ferrous and ferric ions in their structure. GRs can potentially serve as a chemical reductant for degradation of chlorinated hydrocarbons. GRs are found in zerovalent iron based permeable reactive barriers and in c...

  12. A marine sink for chlorine in natural organic matter

    Science.gov (United States)

    Leri, Alessandra C.; Mayer, Lawrence M.; Thornton, Kathleen R.; Northrup, Paul A.; Dunigan, Marisa R.; Ness, Katherine J.; Gellis, Austin B.

    2015-08-01

    Chloride--the most abundant ion in sea water--affects ocean salinity, and thereby seawater density and ocean circulation. Its lack of reactivity gives it an extremely long residence time. Other halogens are known to be incorporated into marine organic matter. However, evidence of similar transformations of seawater chloride is lacking, aside from emissions of volatile organochlorine by marine algae. Here we report high organochlorine concentrations from 180 to 700 mg kg-1 in natural particulate organic matter that settled into sediment traps at depths between 800 and 3,200 m in the Arabian Sea, taken between 1994 and 1995. X-ray spectromicroscopic imaging of chlorine bonding reveals that this organochlorine exists primarily in concentrated aliphatic forms consistent with lipid chlorination, along with a more diffuse aromatic fraction. High aliphatic organochlorine in particulate material from cultured phytoplankton suggests that primary production is a source of chlorinated organic matter. We also found that particulate algal detritus can act as an organic substrate for abiotic reactions involving Fe2+, H2O2 or light that incorporate chlorine into organic matter at levels up to several grams per kilogram. We conclude that transformations of marine chloride to non-volatile organochlorine through biological and abiotic pathways represent an oceanic sink for this relatively unreactive element.

  13. Riverine input of chlorinated hydrocarbons in the coastal pollution

    Digital Repository Service at National Institute of Oceanography (India)

    Sarkar, A.; Everaarts, J.M.

    of various chlorinated hydrocarbons. It deals with an in-depth analysis of pollution of the coastal ecosystem around the Netherlands, U.K. and Germany due to inputs of contaminants from the rivers namely, Elbe, Weser, Ems Ijssel, Rhine, Meuse, Scheldt, Thames...

  14. Inactivation of human and simian rotaviruses by chlorine dioxide

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Yu-Shiaw (Brookhaven National Lab., Upton, NY (USA)); Vaughn, J.M. (Univ. of New England College of Medicine, Biddeford, ME (USA))

    1990-05-01

    The inactivation of single-particle stocks of human (type 2, Wa) and simian (SA-11) rotaviruses by chlorine dioxide was investigated. Experiments were conducted at 4{degree}C in a standard phosphate-carbonate buffer. Both virus types were rapidly inactivated, within 20 s under alkaline conditions, when chlorine dioxide concentrations ranging from 0.05 to 0.2 mg/liter were used. Similar reductions of 10{sup 5}-fold in infectivity required additional exposure time of 120 s at 0.2 mg/liter for Wa and at 0.5 mg/liter for SA-11, respectively, at pH 6.0. The inactivation of both virus types was moderate a neutral pH, and the sensitivities to chlorine dioxide were similar. The observed enhancement of virucidal efficiency with increasing pH was contrary to earlier findings with chlorine- and ozone-treated rotavirus particles, where efficiencies decreased with increasing alkalinity. Comparison of 99.9% virus inactivation times revealed ozone to be the most effective virucidal agent among these three disinfectants.

  15. Processing of molybdenite concentrates by low-temprature chlorination roasting

    OpenAIRE

    Александров, Павло Володимирович

    2012-01-01

    Prospects of low-temperature chlorination roasting with chlorides of alkaline metals application for processing of molybdenite concentrate are shown. General benefits of it are reduction of evolving of dioxide of sulfur in the atmosphere, reduction of roasting temperature to 450 ºС and formation of water-soluble compounds of molybdenum during roasting

  16. Inhibition of lipopolysaccharide induced acute inflammation in lung by chlorination.

    Science.gov (United States)

    Zhang, Jinshan; Xue, Jinling; Xu, Bi; Xie, Jiani; Qiao, Juan; Lu, Yun

    2016-02-13

    Lipopolysaccharide (LPS, also called endotoxin) is a pro-inflammatory constituent of gram negative bacteria and cyanobacteria, which causes a potential health risk in the process of routine urban application of reclaimed water, such as car wash, irrigation, scenic water refilling, etc. Previous studies indicated that the common disinfection treatment, chlorination, has little effect on endotoxin activity removal measured by Limulus amebocyte lysate (LAL) assay. However, in this study, significant decrease of acute inflammatory effects was observed in mouse lung, while LAL assay still presented a moderate increase of endotoxin activity. To explore the possible mechanisms, the nuclear magnetic resonance (NMR) results showed the chlorination happened in alkyl chain of LPS molecules, which could affect the interaction between LPS and LPS-binding protein. Also the size of LPS aggregates was found to drop significantly after treatment, which could be another results of chlorination caused polarity change. In conclusion, our observation demonstrated that chlorination is effective to reduce the LPS induced inflammation in lung, and it is recommended to use health effect-based methods to assess risk removal of water treatment technologies. PMID:26530889

  17. EFFECTS OF CONTINUOUS CHLORINATION ON ENTRAINED ESTUARINE PLANKTON

    Science.gov (United States)

    The effects of continuous chlorination on entrained plankton are investigated in tests using running sea water and adenosine triphosphate (ATP) as an indicator of biomass. Effects were measured by bioluminescence with the use of luciferin-luciferase reagents from firefly lanterns...

  18. Disinfection byproduct yields from the chlorination of natural waters

    Science.gov (United States)

    Rathbun, R.E.

    1996-01-01

    Yields for the formation of trihalomethane and nonpurgeable total organic-halide disinfection byproducts were determined as a function of pH and initial free-chlorine concentration for the chlorination of water from the Mississippi, Missouri, and Ohio Rivers. Samples were collected at 12 sites on the Mississippi River from Minneapolis, MN, to New Orleans. LA, and on the Missouri and Ohio Rivers 1.6 km above their confluences with the Mississippi during the summer, fall, and spring seasons of the year. Yields varied little with distance along the Mississippi River, although the dissolved organic-carbon concentration decreased considerably with distance downstream. Yields for the Missouri and Ohio were comparable to yields for the Mississippi, despite much higher bromide concentrations for the Missouri and Ohio. Trihalomethane yields increased as the pH and initial free- chlorine concentration increased. Nonpurgeable total organic-halide yields also increased as the initial free-chlorine concentration increased, but decreased as the pH increased.

  19. Clustering chlorine reactivity of haloacetic acid precursors in inland lakes.

    Science.gov (United States)

    Zeng, Teng; Arnold, William A

    2014-01-01

    Dissolved organic matter (DOM) represents the major pool of organic precursors for harmful disinfection byproducts, such as haloacetic acids (HAAs), formed during drinking water chlorination, but much of it remains molecularly uncharacterized. Knowledge of model precursors is thus a prerequisite for understanding the more complex whole water DOM. The utility of HAA formation potential data from model DOM precursors, however, is limited due to the lack of comparability to water samples. In this study, the formation kinetics of dichloroacetic acid (DCAA) and trichloroacetic acid (TCAA), the two predominant HAA species, were delineated upon chlorination of seventeen model DOM precursors and sixty-eight inland lake water samples collected from the Upper Midwest region of the United States. Of particular interest was the finding that the DCAA and TCAA formation rate constants could be grouped into four statistically distinct clusters reflecting the core structural features of model DOM precursors (i.e., non-β-diketone aliphatics, β-diketone aliphatics, non-β-diketone phenolics, and β-diketone phenolics). A comparative approach built upon hierarchical cluster analysis was developed to gain further insight into the chlorine reactivity patterns of HAA precursors in inland lake waters as defined by the relative proximity to four model precursor clusters. This work highlights the potential for implementing an integrated kinetic-clustering approach to constrain the chlorine reactivity of DOM in source waters.

  20. Controlled Burning of Forest Detritus Altering Spectroscopic Characteristics and Chlorine Reactivity of Dissolved Organic Matter: Effects of Temperature and Oxygen Availability.

    Science.gov (United States)

    Wang, Jun-Jian; Dahlgren, Randy A; Chow, Alex T

    2015-12-15

    Forest fires occur with increasing frequency and severity in the western United States, potentially altering the chemistry and quantity of dissolved organic matter (DOM) and disinfection byproduct (DBP) precursors exported from forested watersheds. However, little is known concerning effects of the fire triangle (heat, oxygen, and fuel) on DOM alteration. Using detritus from Pinus ponderosa and Abies concolor (dominant species in forests in the western United States), we prepared DOM from unburned and burned detritus under hypoxic (pyrolysis) and oxic conditions (thermal oxidation) at 250 and 400 °C. DOM characteristics and chlorine reactivity were evaluated by absorption and fluorescence spectroscopy and chlorination-based DBP formation potential tests. Spectroscopic results suggest that burned-detritus extracts had lower molecular weight (reflected by increased E2:E3 and fluorescence index) and divergent aromaticity (reflected by SUVA254) depending on oxygen availability. Temperature and oxygen availability interacted to alter the chlorine reactivity of fire-affected DOM. Increasing temperature from 50 to 400 °C resulted in decreased reactivities for trihalomethane and chloral hydrate formation and divergent reactivities for haloacetonitrile formation (unchanged for pyrolysis and increased for oxidation) and haloketone formation (increased for pyrolysis and decreased for oxidation). We demonstrate that DBP precursors in fire-affected forest detritus are highly dependent on temperature and oxygen availability. PMID:26496434

  1. Impact of January 2005 solar proton events on chlorine species

    Directory of Open Access Journals (Sweden)

    A. Damiani

    2012-01-01

    Full Text Available Sudden changes in stratospheric chlorine species in the polar northern atmosphere, caused by the Solar Proton Events (SPEs of 17 and 20 January 2005, have been investigated and compared with version 4 of the Whole Atmosphere Community Climate Model (WACCM4. We used Aura Microwave Limb Sounder (MLS measurements to monitor the variability of ClO, HCl, HOCl and Michelson Interferometer for Passive Atmospheric Sounder (MIPAS on ENVISAT to retrieve ClONO2. SPE-induced chlorine activation has been identified. HCl decrease occurred at nearly all the investigated altitudes with the lowest values (of less than 0.25 ppbv on 21 January. HOCl was found to be the main active chlorine species under nighttime conditions (with increases of more than 0.2 ppbv whereas both HOCl and ClO enhancements (about 0.1 ppbv have been observed at the polar night terminator. Further, small ClO decreases (of less than 0.1 ppbv and ClONO2 enhancements (about 0.2 ppbv have been observed at higher latitudes (i.e., at nighttime roughly above 2 hPa.

    While WACCM4 reproduces most of the SPE-induced variability in the chlorine species fairly well, in some particular regions discrepancies between the modeled and measured temporal evolution of the abundances of chlorine species were found. HOCl changes are modelled very well with respect to both magnitude and geographic distribution. ClO decreases are reproduced at high latitudes, whereas ClO enhancements in the terminator region are underestimated and attributed to background variations. WACCM4 also reproduces the HCl depletion in the mesosphere but it does not show the observed decrease below about 2 hPa. Finally, WACCM4 simulations indicate that the observed ClONO2 increase is dominated by background variability, although SPE-induced production might contribute by 0.1 ppbv.

  2. Bulk chlorine uptake by polyamide active layers of thin-film composite membranes upon exposure to free chlorine-kinetics, mechanisms, and modeling.

    Science.gov (United States)

    Powell, Joshua; Luh, Jeanne; Coronell, Orlando

    2014-01-01

    We studied the volume-averaged chlorine (Cl) uptake into the bulk region of the aromatic polyamide active layer of a reverse osmosis membrane upon exposure to free chlorine. Volume-averaged measurements were obtained using Rutherford backscattering spectrometry with samples prepared at a range of free chlorine concentrations, exposure times, and mixing, rinsing, and pH conditions. Our volume-averaged measurements complement previous studies that have quantified Cl uptake at the active layer surface (top ≈ 7 nm) and advance the mechanistic understanding of Cl uptake by aromatic polyamide active layers. Our results show that surface Cl uptake is representative of and underestimates volume-averaged Cl uptake under acidic conditions and alkaline conditions, respectively. Our results also support that (i) under acidic conditions, N-chlorination followed by Orton rearrangement is the dominant Cl uptake mechanism with N-chlorination as the rate-limiting step; (ii) under alkaline conditions, N-chlorination and dechlorination of N-chlorinated amide links by hydroxyl ion are the two dominant processes; and (iii) under neutral pH conditions, the rates of N-chlorination and Orton rearrangement are comparable. We propose a kinetic model that satisfactorily describes Cl uptake under acidic and alkaline conditions, with the largest discrepancies between model and experiment occurring under alkaline conditions at relatively high chlorine exposures. PMID:24506252

  3. Chlorinated Hydrocarbon Degradation in Plants: Mechanisms and Enhancement of Phytoremediation of Groundwater Contamination

    Energy Technology Data Exchange (ETDEWEB)

    Stuart Strand

    2004-09-27

    The research objectives for this report are: (1) Transform poplar and other tree species to extend and optimize chlorinated hydrocarbon (CHC) oxidative activities. (2) Determine the mechanisms of CHC oxidation in plants. (3) Isolate the genes responsible for CHC oxidation in plants. We have made significant progress toward an understanding of the biochemical mechanism of CHC transformation native to wild-type poplar. We have identified chloral, trichloroethanol, trichloroacetic acid, and dichloroacetic acid as products of TCE metabolism in poplar plants and in tissue cultures of poplar cells.(Newman et al. 1997; Newman et al. 1999) Use of radioactively labeled TCE showed that once taken up and transformed, most of the TCE was incorporated into plant tissue as a non-volatile, unextractable residue.(Shang et al. 2001; Shang and Gordon 2002) An assay for this transformation was developed and validated using TCE transformation by poplar suspension cells. Using this assay, it was shown that two different activities contribute to the fixation of TCE by poplar cells: one associated with cell walls and insoluble residues, the other associated with a high molecular weight, heat labile fraction of the cell extract, a fixation that was apparently catalyzed by plant enzymes.

  4. Mutagenic activity associated with by-products of drinking water disinfection by chlorine, chlorine dioxide, ozone and UV-irradiation.

    Science.gov (United States)

    Zoeteman, B C; Hrubec, J; de Greef, E; Kool, H J

    1982-12-01

    A retrospective epidemiological study in The Netherlands showed a statistical association between chlorination by-products in drinking water and cancer of the esophagus and stomach for males. A pilot-plant study with alternative disinfectants was carried out with stored water of the Rivers Rhine and Meuse. It was demonstrated that the increase of direct acting mutagens after treatment with chlorine dioxide is similar to the effect of chlorination. Ozonation of Rhine water reduced the mutagenic activity for Salmonella typhimurium TA 98 both with and without metabolic activation. UV alone hardly affects the mutagenicity of the stored river water for S. typh. TA 98. In all studies, practically no mutagenic activity for S. typh. TA 100 was found. Although remarkable changes in the concentration of individual organic compounds are reported, the identity of the mutagens detected is yet unclear. Compounds of possible interest due to their removal by ozonation are 1,3,3-trimethyloxindole, dicyclopentadiene and several alkylquinolines. Compounds which might be responsible for the increased mutagenicity after chlorination are two brominated acetonitriles and tri(2-chlorethyl) phosphate. Furthermore, the concentration procedure with adsorption on XAD resin and the subsequent elution step may have affected the results. It is proposed to focus further research more on the less volatile by-products of disinfection than on the trihalomethanes.

  5. Degradation mechanisms of geosmin and 2-MIB during UV photolysis and UV/chlorine reactions.

    Science.gov (United States)

    Kim, Tae-Kyoung; Moon, Bo-Ram; Kim, Taeyeon; Kim, Moon-Kyung; Zoh, Kyung-Duk

    2016-11-01

    We conducted chlorination, UV photolysis, and UV/chlorin reactions to investigate the intermediate formation and degradation mechanisms of geosmin and 2-methylisoborneol (2-MIB) in water. Chlorination hardly removed geosmin and 2-MIB, while the UV/chlorine reaction at 254 nm completely removed geosmin and 2-MIB within 40 min and 1 h, respectively, with lesser removals of both compounds during UV photolysis. The kinetics during both UV photolysis and UV/chlorine reactions followed a pseudo first-order reaction. Chloroform was found as a chlorinated intermediate during the UV/chlorine reaction of both geosmin and 2-MIB. The pH affected both the degradation and chloroform production during the UV/chlorine reaction. The open ring and dehydration intermediates identified during UV/chlorine reactions were 1,4-dimethyl-adamantane, and 1,3-dimethyl-adamantane from geosmin, 2-methylenebornane, and 2-methyl-2-bornene from 2-MIB, respectively. Additionally, 2-methyl-3-pentanol, 2,4-dimethyl-1-heptene, 4-methyl-2-heptanone, and 1,1-dichloro-2,4-dimethyl-1-heptane were newly identified intermediates from UV/chlorine reactions of both geosmin and 2-MIB. These intermediates were degraded as the reaction progressed. We proposed possible degradation pathways during the UV photolysis and UV/chlorine reactions of both compounds using the identified intermediates.

  6. Simultaneous Control of Microorganisms and Disinfection By-products by Sequential Chlorination

    Institute of Scientific and Technical Information of China (English)

    CHAO CHEN; XIAO-JIAN ZHANG; WEN-JIE HE; HONG-DA HAN

    2007-01-01

    Objective To introduce a new sequential chlorination disinfection process in which short-term free chlorine and chloramine are sequentially added. Methods Pilot tests of this sequential chlorination were carried out in a drinking water plant. Results The sequential chlorination disinfection process had the same or better efficiency on microbe (including virus)inactivation compared with the free chlorine disinfection process. There seemed to be some synergetic disinfection effect between free chlorine and monochloramine because they attacked different targets. The sequential chlorination disinfection process resulted in 35.7%-77.0% TTHM formation and 36.6%-54.8% THAA5 formation less than the free chlorination process.The poorer the water quality was, the more advantage the sequential chlorination disinfection had over the free chlorination.Conclusion This process takes advantages of free chlorine's quick inactivation of microorganisms and chloramine's low disinfection by-product (DBP) yield and long-term residual effect, allowing simultaneous control of microbes and DBPs in an effective and economic way.

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

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

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

  8. Polychlorinated biphenyl toxicity to Japanese quail as related to degree of chlorination

    Science.gov (United States)

    Hill, E.F.; Heath, R.G.; Spann, J.W.; Williams, J.D.

    1974-01-01

    To learn if the percentage of chlorine in a mixture of polychlorinated biphenyls (PCB's) alone determines toxicity, Japanese quail were fed diets containing Aroelor 1248, 1254, or 1260 at levels that added equal amounts of chlorine to the feed. The experiment comprised two consecutive 5-day periods; three sublethal concentrations of chlorine were evaluated during the first period and three lethal concentrations during the second period. Evaluations utilized comparisons of mortality, time to death, weight change, and food consumption. Sublethal concentrations produced no detectable effects. Lethal concentrations with equal Chlorine showed Aroelor 1248 to be less toxic at the highest chlorine concentrations, but at lower concentrations Aroelor 1254 was more toxic than Aroclor 1260. Although chlorine percentage of a PCB is positively correlated with its avian toxicity, PCB toxicity is apparently not simply a function of chlorination.

  9. Direct chlorination process for geothermal power plant off-gas - hydrogen sulfide abatement

    Energy Technology Data Exchange (ETDEWEB)

    Sims, A.V.

    1983-06-01

    The Direct Chlorination Process removes hydrogen sulfide from geothermal off-gases by reacting hydrogen sulfide with chlorine in the gas phase. Hydrogen chloride and elemental sulfur are formed by this reaction. The Direct Chlorination Process has been successfully demonstrated by an on-site operation of a pilot plant at the 3 M We HPG-A geothermal power plant in the Puna District on the island of Hawaii. Over 99.5 percent hydrogen sulfide removal was achieved in a single reaction state. Chlorine gas did not escape the pilot plant, even when 90 percent excess chlorine gas was used. A preliminary economic evaluation of the Direct Chlorination Process indicates that it is very competitive with the Stretford Process. Compared to the Stretford Process, the Direct Chlorination Process requires about one-third the initial capital investment and about one-fourth the net daily expenditure.

  10. Fate of chlorinated fatty acids in migrating sockeye salmon and their transfer to arctic grayling

    DEFF Research Database (Denmark)

    Mu, Huiling; Ewald, G.; Nilsson, E.;

    2004-01-01

    organohalogen compounds in the salmon were halogenated fatty acids, predominantly chlorinated species that accounted for up to 35% of the extractable, organically bound chlorine (EOCl) in the fish tissues. The amount of chlorinated fatty acids in the salmon muscle decreased as a result of spawning migration....... The decrease was correlated with that of triacylglycerols in the salmon muscle, indicating the chlorinated fatty acids to be mobilized and metabolized to approximately the same extent as the other fatty acids. Chlorinated fatty acids were also transferred to the maturing roe in a manner similar...... to that of the unchlorinated fatty acids. Lipids of the Arctic grayling (Thymallus arcticus), a fish resident to the spawning lake of the salmon, contained higher concentrations of chlorinated fatty acids than grayling in a lake without migratory salmon. This may reflect a food-chain transfer of the chlorinated fatty acids...

  11. Effect of oxidation on nitro-based pharmaceutical degradation and trichloronitromethane formation.

    Science.gov (United States)

    Wang, Xiaofeng; Zhou, Beihai; Yang, Hongwei; Wang, Xiaomao; Xie, Yuefeng

    2016-03-01

    Nitro-based compounds are the direct precursors of trichloronitromethane during chlorination disinfection. Two nitro-based pharmaceuticals ranitidine and nizatidine were selected as model compounds to assess the effect of oxidation on the removal of nitro-based pharmaceuticals, as well as the reduction of their trichloronitromethane formation potentials (TCNMFPs). The four oxidants were ozone (O3), chlorine (Cl2), chlorine dioxide (ClO2) and potassium permanganate (KMnO4). The changes in pharmaceuticals and their TCNMFPs during oxidation using various oxidants and dosages were quantified. The relationships between oxidation product structures and TCNMFP changes were also analyzed. The results showed that oxidation with Cl2 and KMnO4 were more effective than ClO2 and O3 in removing the nitro-based pharmaceuticals. Meanwhile, decreased TCNMFPs by KMnO4 oxidation but increased TCNMFPs by Cl2, ClO2 and O3 oxidation were observed. The results of product analysis indicated that chlorine transfer products had higher TCNMFPs, while oxygen transfer products made little contribution to TCNMFPs after oxidation. In addition, one possible reaction pathway leading TCNMFP increase was that chloro-nitromethane or nitromethane, which was a better TCNM precursor, formed when double bond was attacked by oxidants. PMID:26714298

  12. Formation of trichloromethane in chlorinated water and fresh-cut produce and as a result of reacting with citric acid

    Science.gov (United States)

    Chlorine (sodium hypochlorite) is commonly used by the fresh produce industry to sanitize wash water, fresh and fresh-cut fruits and vegetables. However, possible formation of harmful chlorine by-products is a concern. The objectives of this study were to compare chlorine and chlorine dioxide in t...

  13. Durability of Selected Membrane Materials when Exposed to Chlorine Gas

    Energy Technology Data Exchange (ETDEWEB)

    Eikeland, Marianne Soerflaten

    2001-03-01

    This thesis is focusing on the durability of selected membrane materials when exposed to chlorine gas in the temperature range 30-100{sup o}C. Studies of the changes of membrane separation properties and the mechanisms promoting these changes have been studied. The selected membrane materials were poly(dimethylsioxane) (PDMS), Fluorel, fluorosilicone, and blends of PDMS and Fluorel. The thesis is organised in seven chapters. The first chapter gives an introduction to the background of the work. The second chapter presents the theory for gas separation using dense rubbery membranes. The properties of the selected membrane materials are presented in chapter three. The fourth chapter describes degradation mechanisms for polymeric materials in general and for the selected membrane materials in particular. Presentation of the experimental work is given in chapter five, while the results with discussions are presented in chapter six. The conclusions and recommendations for further studies are given in chapter seven. Five appendixes are attached: Appendix A describes the calculations of permeability and solubility coefficients and the accuracy of the experimental measurements. Appendix B summarises the measured values in tables and Appendix C describes the analytical methods. Appendix D gives the properties of the gases used in the experiments. Appendix E is the article ''Durability of Poly(dimethylsiloxane) when Exposed to Chlorine Gas'', submitted to the Journal of Applied Polymer Science. Highly crosslinked PDMS was found to have an initial high permeability for chlorine gas and a high Cl{sub 2}/O{sub 2} selectivity. However when exposed to chlorine gas the permeability decreased significantly. Crosslinking of the PDMS polymer chain and chlorination of the polymer gave a denser polymer structure and thus lower permeability. Fluorel showed very low permeabilities and selectivities for the gases in question and was thus not interesting for this

  14. Evaluation of cooling water treatment programme at RAPS-3 and 4 with reference to chlorination and microbial control

    International Nuclear Information System (INIS)

    Water from Rana Pratap Sagar Lake is used in Rajasthan Atomic Power Station (RAPS) units 3 and 4 for cooling the condenser system. As the lake water is rich in nutrients and microflora, investigations were carried out on the nutrient quality, microflora distribution and chlorine decay to evaluate the cooling water treatment programme. Algal growth in emergency storage makeup water pools, weed growth on the cooling tower decks and biofilm growth on various materials (carbon steel, stainless steel, admiralty brass and cupronickel) were studied with an objective to understand the reasons for corrosion and failure of fire water pipeline. Visual examination showed that the emergency makeup water pools were infested with green algae and cyano-bacterial mats. Some algal growth was observed on induced draft cooling tower-3 structures. The bacterial counts in various water samples were low, except in emergency makeup water pool. Sulphate reducing bacteria (SRB) were present in makeup and demineralised waters. Chlorophyll pigment analysis showed that the makeup and emergency storage water pool had abundant algal growth. To prevent biofouling, chlorine is dosed at the rate of 7 kg/hr for 10 minutes; free residual oxidant (FRO) and chlorine decay were monitored at regular intervals. After 24 hrs, biofilm thickness on different materials ranged from 27-45 μm. However, the thickness was reduced by 50 % after exposure to 2 ppm of chlorine for 15 minutes. In further investigations, it was found that the anion resin beads of demineraliser plant were infested with filamentous microbes. Hence, It is recommended to treat the feed water of DM plant. Tubercles were observed inside the failed fire water carbon steel pipeline and on removing the tubercles concentric ring patterns, typical signatures of SRB corrosion were observed. For controlling the biofouling problem in the cooling water system, it is recommended to maintain a chlorine dose of 2.3 ppm (which gives 0.8 ppm FRO) for two

  15. Comparison of various advanced oxidation processes for the degradation of phenylurea herbicides.

    Science.gov (United States)

    Kovács, Krisztina; Farkas, János; Veréb, Gábor; Arany, Eszter; Simon, Gergő; Schrantz, Krisztina; Dombi, András; Hernádi, Klára; Alapi, Tünde

    2016-01-01

    Various types of advanced oxidation processes (AOPs), such as UV photolysis, ozonation, heterogeneous photocatalysis and their combinations were comparatively examined at the same energy input in a home-made reactor. The oxidative transformations of the phenylurea herbicides fenuron, monuron and diuron were investigated. The initial rates of transformation demonstrated that UV photolysis was highly efficient in the cases of diuron and monuron. Ozonation proved to be much more effective in the transformation of fenuron than in those of the chlorine containing monuron and diuron. In heterogeneous photocatalysis, the rate of decomposition decreased with increase of the number of chlorine atoms in the target molecule. Addition of ozone to UV-irradiated solutions and/or TiO2-containing suspensions markedly increased the initial rates of degradation. Dehalogenation of monuron and diuron showed that each of these procedures is suitable for the simultaneous removal of chlorinated pesticides and their chlorinated intermediates. Heterogeneous photocatalysis was found to be effective in the mineralization.

  16. Interactively interfacial reaction of iron-reducing bacterium and goethite for reductive dechlorination of chlorinated organic compounds

    Institute of Scientific and Technical Information of China (English)

    LI XiaoMin; LI YongTao; LI FangBai; ZHOU ShunGui; FENG ChunHua; LIU TongXu

    2009-01-01

    The interactively interfacial reactions between the iron-reducing bacterium (Shewanella decolorationis,S12) and iron oxide (α-FeOOH) were investigated to determine reductive dechlorination transformation of chlorinated organic compounds (chloroform and pentachlorophenol).The results showed that the interactive system of S12+ α-FeOOH exhibited relatively high dechlorination rate.By comparison,the S12 biotic system alone had no obvious dechlorination,and the α-FeOOH abiotic system showed low dechlorination rate.The enhanced dechlorination of chloroform and pentachlorophenol in the interactive system of S12+α-FeOOH was derived from the promoted generation of adsorbed Fe(Ⅱ) by S12.A decrease in redox potential of the Fe (Ⅲ)/Fe (Ⅱ) couple in the interactive reaction system was determined by cyclic voltammetry.Our results will give new insight into interactively interfacial reaction between iron-reducing bacterium and iron oxides for degradation of chlorinated organic compounds under anaerobic condition.

  17. Study of removal effect on Mesocyclops leukarti with oxidants

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Cyclops of zooplankton propagates prolifically in eutrophic waterbody and it cannot be exterminated by conventional disinfection process. The mutagenicity of Mesocyclops leukarti and its extermination with oxidants in a drinking waterworks in China were studied. Among five oxidants for use in bench-scale, chlorine dioxide is the most effective and the potassium permanganate is the weakest against Mesocyclops leukarti under the same conditions. Full-scale results showed that Mesocyclops leukarti could be effectively removed from water by 1.0 mg/L chlorine dioxide preoxidation combined with conventional removal physical process. After filtration, chlorite, a by-product of prechlorine dioxide, is stable at 0.45 mg/L, which is lower than the critical value of the USEPA. GC-MS examination and Ames test further showed that the quantity of organic substance and the mutagenicity in water treated by chlorine dioxide preoxidation are obviously less than those of prechlorination.

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

    Science.gov (United States)

    Ufermann, Petra; Petersen, Hauke; Exner, Martin

    2011-12-01

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

  19. Stepwise Chlorination-Chemical Vapor Transport Reactions for Bastnaesite Concentrate

    Institute of Scientific and Technical Information of China (English)

    张丽清; 王军; 范世华; 雷鹏翔; 王之昌

    2002-01-01

    Vapor phase extraction and mutual separation of rare earth (RE) elements from bastnaesite concentrate were investigated using stepwise chlorination-chemical vapor transport reactions mediated by vapor complexes LnAlnCl3n+3 (Ln=RE elements). The bastnaesite was heated to 800 K and chlorinated between 800~1300 K with C+Cl2+SiCl4 to remove CO2, SiF4 and high volatile chlorides. At the temperature of 1300 K for 6 h, the resulted RE chlorides were chemically transported and mutual separated with the vapor complexes while CaCl2 and BaCl2 were remained in the residues. Significantly different CVT characteristics were observed for gradually decreased and wave form temperature gradients

  20. Pressured liquid chlorine leakage accident simulation in highway tunnel

    Directory of Open Access Journals (Sweden)

    LI Jianfeng, LIU Mao, WANG Wei

    2010-03-01

    Full Text Available With the national economic development, China's transportation infrastructure has also made great progress, particularly in the highway. How to reduce the accident consequence that occurred in the highway tunnel has been the tropical topic in China. The liquid Chlorine accidental leakage in highway tunnel was exemplified for the poisonous gas dispersion consequence analysis using computational fluid dynamics. First, the GAMBIT code was used to create geometrical models and generate meshes. Second, by using the FLUENT code, the Chlorine gas dispersion in the highway tunnel was simulated and the scenarios with different leak sources were discussed. Case study shows that the FLUENT code was useful on the simulation of gas dispersion in highway tunnel that serves the prerequisite for the further research.

  1. Chlorine trifluoride (1963); Le trifluorure de chlore (1963)

    Energy Technology Data Exchange (ETDEWEB)

    Vincent, L.M.; Gillardeau, J. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1963-07-01

    This monograph on chlorine trifluoride may be considered as a working tool useful in gaseous diffusion research. It consists of data gathered from the literature and includes furthermore a certain amount of original data. This monograph groups together the physical, chemical and physiological properties of chlorine trifluoride, as well as the preparation and analytical methods. It has been thought wise to add some technological information, and the safety regulations governing its use. (authors) [French] Cette monographie sur le trifluorure de chlore doit etre consideree comme un instrument de travail dans le cadre des recherches sur la diffusion gazeuse. Il etait necessaire de grouper les donnees eparses dans la litterature. Elle comprend en outre un certain nombre de donnees originales. Cette monographie groupe les proprietes physiques, chimiques et physiologiques du trifluorure de chlore, ainsi que ses methodes de preparation et d'analyse. On a juge utile de joindre des indications technologiques et les consignes de securite concernant son emploi. (auteurs)

  2. Gas Phase Sulfur, Chlorine and Potassium Chemistry in Biomass Combustion

    DEFF Research Database (Denmark)

    Løj, Lusi Hindiyarti

    2007-01-01

    Gas Phase Sulfur, Chlorine and Alkali Metal Chemistry in Biomass Combustion Concern about aerosols formation, deposits, corrosion, and gaseous emissions during biomass combustion, especially straw, continues to be a driving force for investigation on S, Cl, K-containing species under combustions...... conditions. These trace species contained in the biomass structure will be released to the gas phase during combustion and contribute to the problems generated during the process. The investigation during this PhD project is done to stepwise improve the understanding in the chemistry and reduce...... the uncertainties. In the present work, the detailed kinetic model for gas phase sulfur, chlorine, alkali metal, and their interaction has been updated. The K/O/H/Cl chemistry, S chemistry, and their interaction can reasonably predict a range of experimental data. In general, understanding of the interaction...

  3. Biodegradation of Chlorinated Solvents: Reactions near DNAPL and Enzyme Function

    International Nuclear Information System (INIS)

    Chlorinated solvents are among the most widespread groundwater contaminants in the country, contamination which is also among the most difficult and expensive for remediation. These solvents are biodegradable in the absence of oxygen, but this biodegradation requires both a food source for the organisms (electron donor) and the presence of chlorinated solvent biodegrading organisms. These two requirements are present naturally at some contamination sites, leading to natural attenuation of the solvents. If one or both requirements are absent, then engineered bioremediation either through addition of an external electron donor or through bioaugmentation with appropriate microorganisms, or both, may be used for site remediation. The most difficult case for cleanup is when a large residual of undissolved chlorinated solvents are present, residing as dense -non-aqueous-phase- liquid ( DNAPL). A major focus of this study was on the potential for biodegradation of the solvents when pre sent as DNAPL where concentrations are very high and potential for toxicity to microorganisms exist. Another focus was on a better understanding of the biological mechanisms involved in chlorinated solvent biodegradation . These studies were directed towards the chlorinated solvents, trichloroethene (TCE), tetrachloroethene or perchloroethene (PCE), and carbon tetrachloride (CT). The potential for biodegradation of TCE and PCE DNAPL was clearly demonstrated in this research. From column soil studies and batch studies we found there to be a clear advantage in focusing efforts at bioremediation near the DNAPL. Here, chlorinated solvent concentrations are the highest, both because of more favorable reaction kinetics and because such high solvent concentrations are toxic to microorganisms, such as methanogens, which compete with dehalogenators for the electron donor. Additionally, biodegradation near a PCE DNAPL results in an enhanced dissolution rate for the chlorinated solvent, by factors of

  4. MECHANISM OF CHLORATE FORMATION IN CHLORINE DIOIXDE DELIGNIFICATION

    Institute of Scientific and Technical Information of China (English)

    Byung-HoYoon; Li-JunWangI; Se-JongKim

    2004-01-01

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

  5. Biodegradation of Chlorinated Solvents: Reactions near DNAPL and Enzyme Function

    Energy Technology Data Exchange (ETDEWEB)

    McCarty, P. L.; Spormann, Alfred M.; Criddle, Craig, S.

    2003-12-11

    Chlorinated solvents are among the most widespread groundwater contaminants in the country, contamination which is also among the most difficult and expensive for remediation. These solvents are biodegradable in the absence of oxygen, but this biodegradation requires both a food source for the organisms (electron donor) and the presence of chlorinated solvent biodegrading organisms. These two requirements are present naturally at some contamination sites, leading to natural attenuation of the solvents. If one or both requirements are absent, then engineered bioremediation either through addition of an external electron donor or through bioaugmentation with appropriate microorganisms, or both, may be used for site remediation. The most difficult case for cleanup is when a large residual of undissolved chlorinated solvents are present, residing as dense -non-aqueous-phase- liquid ( DNAPL). A major focus of this study was on the potential for biodegradation of the solvents when pre sent as DNAPL where concentrations are very high and potential for toxicity to microorganisms exist. Another focus was on a better understanding of the biological mechanisms involved in chlorinated solvent biodegradation . These studies were directed towards the chlorinated solvents, trichloroethene (TCE), tetrachloroethene or perchloroethene (PCE), and carbon tetrachloride (CT). The potential for biodegradation of TCE and PCE DNAPL was clearly demonstrated in this research. From column soil studies and batch studies we found there to be a clear advantage in focusing efforts at bioremediation near the DNAPL. Here, chlorinated solvent concentrations are the highest, both because of more favorable reaction kinetics and because such high solvent concentrations are toxic to microorganisms, such as methanogens, which compete with dehalogenators for the electron donor. Additionally, biodegradation near a PCE DNAPL results in an enhanced dissolution rate for the chlorinated solvent, by factors of

  6. Biodegradation of chlorinated solvents in a water unsaturated topsoil

    DEFF Research Database (Denmark)

    Borch, T.; Ambus, P.; Laturnus, F.;

    2003-01-01

    In order to investigate topsoils as potential sinks for chlorinated solvents from the atmosphere, the degradation of trichloromethane (CHCl3), 1,1,1-trichloroethane (CH3CCl3), tetrachloromethane (CCl4), trichloroethene (C2HCl3) and tetrachloroethene (C2Cl4) was studied in anoxic laboratory experi...... after 16 days. Based on the results in this study, we conclude that anaerobic topsoils are potential sinks for these contaminants, and that a natural attenuation potential exists, even in water unsaturated topsoils. (C) 2003 Elsevier Science Ltd. All rights reserved....... experiments designed to simulate denitrifying conditions in water unsanstrated by measuring the release of N-15 in N-2 to the headspace from added N-15 labeled nitrate. The degradation of chlorinated aliphatic compounds was followed by measuring their concentrations in the headspace above the soil...

  7. Environmental Behavior, Sources, and Effects of Chlorinated Polycyclic Aromatic Hydrocarbons

    Directory of Open Access Journals (Sweden)

    Takeshi Ohura

    2007-01-01

    Full Text Available The environmental sources and behaviors of chlorinated 2- to 5-ring polycyclic aromatic hydrocarbons (ClPAHs. ClPAHs are ubiquitous contaminants found in urban air, vehicle exhaust gas, snow, tap water, and sediments. The concentrations of ClPAHs in each of these environments are generally higher than those of dioxins but markedly lower than the concentrations of the parent compounds, PAHs. Environmental data and emission sources analysis for ClPAHs reveal that the dominant process of generation is by reaction of PAHs with chlorine in pyrosynthesis. This secondary reaction process also occurs in aquatic environments. Certain ClPAHs show greater toxicity, such as mutagenicity and aryl hydrocarbon receptor activity, than their corresponding parent PAHs. Investigation of the sources and environmental behavior of ClPAHs is of great importance in the assessment of human health risks.

  8. Field-usable portable analyzer for chlorinated organic compounds

    International Nuclear Information System (INIS)

    In 1992, a chemical sensor was developed which showed almost perfect selectivity to vapors of chlorinated solvents. When interfaced to an instrument, a chemical analyzer will be produced that has near- absolute selectivity to vapors of volatile chlorinated organic compounds. TRI has just completed the second of a 2-phase program to develop this new instrument system, which is called the RCL MONITOR. In Phase II, this instrument was deployed in 5 EM40 operations. Phase II applications covered clean-up process monitoring, environmental modeling, routine monitoring, health and safety, and technology validation. Vapor levels between 0 and 100 ppM can be determined in 90 s with a lower detection limit of 0.5 ppM using the hand-portable instrument. Based on the favorable performance of the RCL MONITOR, the commercial instrument was released for commercial sales on Sept. 20, 1996

  9. Highly chlorinated unintentionally produced persistent organic pollutants generated during the methanol-based production of chlorinated methanes: A case study in China.

    Science.gov (United States)

    Zhang, Lifei; Yang, Wenlong; Zhang, Linli; Li, Xiaoxiu

    2015-08-01

    The formation of unintentionally produced persistent organic pollutants (POPs) may occur during various chlorination processes. In this study, emissions of unintentionally produced POPs during the methanol-based production of chlorinated methanes were investigated. High concentrations of highly chlorinated compounds such as decachlorobiphenyl, octachloronaphthalene, octachlorostyrene, hexachlorobutadiene, hexachlorocyclopentadiene, hexachlorobenzene, and pentachlorobenzene were found in the carbon tetrachloride byproduct of the methanol-based production of chlorinated methanes. The total emission amounts of hexachlorocyclopentadiene, hexachlorobutadiene, polychlorinated benzenes, polychlorinated naphthalenes, octachlorostyrene, and polychlorinated biphenyls released during the production of chlorinated methanes in China in 2010 were estimated to be 10080, 7350, 5210, 427, 212, and 167 kg, respectively. Moreover, polychlorinated dibenzo-p-dioxins (PCDDs), polychlorinated dibenzofurans (PCDFs) were formed unintentionally during chlorinated methanes production, the emission factor for PCDDs/DFs was 364 μg toxic equivalency quotient (TEQ) t(-1) product for residues, which should be added into the UNEP toolkit for updating. It was worth noting that a high overall toxic equivalency quotient from polychlorinated naphthalenes and PCDDs/DFs was generated from the chlorinated methanes production in China in 2010. The values reached 563 and 32.8 g TEQ, respectively. The results of the study indicate that more research and improved management systems are needed to ensure that the methanol-based production of chlorinated methanes can be achieved safely. PMID:25777670

  10. Kinetics of uranium (4) oxidation by oxygen in NaCl-2CsCl melt

    International Nuclear Information System (INIS)

    Using the spectrophotometric method the dependence of the rate of uranium (4) oxidation by the molecular oxygen in NaCl-2CsCl melt upon the value of the specific interface, uranium (4) concentration, the partial pressure of oxygen and chlorine the gas reagent composition and upon the temperature has been found. The kinetic scheme for the reaction in which the interaction of the molecular oxygen with chlorine anions at the melt surface is a slow phase has been proposed

  11. First Derivative UV Spectra of Surface Water as a Monitor of Chlorination in Drinking Water Treatment

    Directory of Open Access Journals (Sweden)

    V. Zitko

    2001-01-01

    Full Text Available Many countries require the presence of free chlorine at about 0.1 mg/l in their drinking water supplies. For various reasons, such as cast-iron pipes or long residence times in the distribution system, free chlorine may decrease below detection limits. In such cases it is important to know whether or not the water was chlorinated or if nonchlorinated water entered the system by accident. Changes in UV spectra of natural organic matter in lakewater were used to assess qualitatively the degree of chlorination in the treatment to produce drinking water. The changes were more obvious in the first derivative spectra. In lakewater, the derivative spectra have a maximum at about 280 nm. This maximum shifts to longer wavelengths by up to 10 nm, decreases, and eventually disappears with an increasing dose of chlorine. The water treatment system was monitored by this technique for over 1 year and changes in the UV spectra of water samples were compared with experimental samples treated with known amounts of chlorine. The changes of the UV spectra with the concentration of added chlorine are presented. On several occasions, water, which received very little or no chlorination, may have entered the drinking water system. The results show that first derivative spectra are potentially a tool to determine, in the absence of residual chlorine, whether or not surface water was chlorinated during the treatment to produce potable water.

  12. Heat inactivation of Escherichia coli O157:H7 in apple juice exposed to chlorine.

    Science.gov (United States)

    Folsom, J P; Frank, J F

    2000-08-01

    Exposure of Escherichia coli O157:H7 to chlorine before heat treatment results in increased production of heat shock proteins. Current heating regimens for pasteurizing apple cider do not account for chlorine exposure in the wash water. This research determined the effect of sublethal chlorine treatment on thermal inactivation of E. coli O157:H7. D58-values were calculated for stationary-phase cells exposed to 0.6 mg/liter of total available chlorine and unchlorinated cells in commercial shelf-stable apple juice (pH 3.6). D58-values for unchlorinated and chlorine-exposed cells in buffer were 5.45 and 1.65 min, respectively (P D58-values calculated from these populations are 0.77 min for unexposed cells and 1.19 min for chlorine-exposed cells (P = 0.05). This indicates that a subpopulation of chorine-treated cells is possibly more resistant to heat because of chlorine treatment. The effect of chlorine treatment, however, is insignificant when compared with the effect of losing the shoulder. This is illustrated by the time required to kill the initial 90% of the cell population. This is observed to be 3.14 min for unchlorinated versus 0.3 min for chlorine-exposed cells (P < 0.001). These observations indicate that current heat treatments need not be adjusted for the effect of chlorine treatment. PMID:10945574

  13. Pandora's Poison: Chlorine, Health, and a New Environmental Strategy

    OpenAIRE

    THORNTON, J.

    2002-01-01

    This book focuses on a group of chemicals, organochlorines, that tops the list of all global and environmental contaminants. The author analyzes the cause and effects of problems associated with producing chlorine-based substances. The book examines organochlorines by looking at major sources, the health impacts on humans and wildlife, and its relation to cancer. The author concludes by suggesting policies and alternatives that can reduce the negative impact of organochlorines.

  14. The pool chlorine hypothesis and asthma among boys.

    LENUS (Irish Health Repository)

    Cotter, A

    2012-01-31

    Swimming pool sanitation has largely been concerned with the microbiological quality of pool water, which is normally treated using a number of chlorine products. Recent studies have pointed to the potential hazards of chlorine by-products to the respiratory epithelium, particularly in indoor, poorly ventilated, pools. The aim of our study was to elucidate whether chronic exposure to indoor chlorinated swimming pools was associated with an increased likelihood of the development of asthma in boys. METHODS: The subjects were boys aged between 6 and 12 years. Data was collected by means of parental responses to a standardized asthma questionnaire (ISAAC: International Study of Asthma and Allergies in Childhood), supplemented with additional questions regarding frequency of attendance, number of years attendance, whether the child is a swimming team member. The questionnaire return rate was 71\\/% (n = 121). 23 boys were excluded on the basis that they had asthma before they started swimming (n = 97). There was a significant association between number of years a boy had been swimming and the likelihood of wheezing in the last 12 months (p = 0.009; OR = 1.351; 95% CI = 1.077-1.693) and diagnosed asthma (p = 0.046; OR = 1.299; 95% CI = 1.004-1.506). The greater the number the number of years a boy had been attending an indoor, chlorinated pool, the greater the likelihood of wheezing in the last 12 months or "had asthma". Age, parental smoking habits and being a swimming team member had no association with any of the asthma variables examined. Swimming pool attendance may be a risk factor in asthma in boys.

  15. Chlorine dioxide against bacteria and yeasts from the alcoholic fermentation

    OpenAIRE

    Meneghin, Silvana Perissatto; Reis, Fabricia Cristina; de Almeida, Paulo Garcia; Ceccato-Antonini, Sandra Regina

    2008-01-01

    The ethanol production in Brazil is carried out by fed-batch or continuous process with cell recycle, in such way that bacterial contaminants are also recycled and may be troublesome due to the substrate competition. Addition of sulphuric acid when inoculum cells are washed can control the bacterial growth or alternatively biocides are used. This work aimed to verify the effect of chlorine dioxide, a well-known biocide for bacterial decontamination of water and equipments, against contaminant...

  16. Flash photolysis of chlorine dioxide in aqueous solution

    International Nuclear Information System (INIS)

    The primary process when aqueous solutions of chlorine dioxide are flash photo-lysed by light with a wave length greater than 270 nm is: OClO →hν ClO (2Π) + O (3P). The photochemical decomposition is characterized by the formation of small quantities of O (3P) atoms and of equal amounts of chlorine atoms and molecular oxygen, the latter originating in the reaction: ClOO → Cl + O2. The isomer ClOO is formed by the germinate recombination of ClO and O, a process which is twice as important as diffusion of the fragments into the mass of the solution and one which represents 30 per cent of the decomposition of the chlorine dioxide. Under our experimental conditions, the lifetime of the ClOO is less than one microsecond. Chlorine atoms are precursors of Cl2O2, whose UV absorption spectrum has been determined, and which is formed by the reactions: Cl + OClO → Cl2O2; Cl + Cl- → Cl2-; Cl2- + OClO → Cl2O2 + Cl- k = (1,0 ±0,1) 109 M-1s-1. Cl2O2 disappears by a first-order process which leads to the formation of the ions Cl- and ClO3-. Competition between the reactions: O (3P) + O2 → O3; O (3P) + OClO → ClO3. (kOClO + O)/(kO2 + O) = 1.85±0.25 has been studied and the molar extinction coefficient of ClO3 determined at its absorption maximum (255 nm): ε255nm = (920 ± 90) M-1 cm-1. (author)

  17. The role of natural chlorinated hydroquinone metabolites in ligninolytic fungi

    OpenAIRE

    Teunissen, P.J.M.

    1999-01-01

    Ligninolytic Basidiomycetes have been reported to produce a wide variety of chloroaromatic compounds as secondary metabolites, which are structurally similar to environmental pollutants. Among these are chlorinated hydroquinone metabolites (CHM), such as 2-chloro-1,4-dimethoxybenzene (2Cl-14DMB), 2,6-dichloro-1,4-dimethoxybenzene (26DCl-14DMB), tetrachloro-1,4-dimethoxybenzene and tetrachloro-4-methoxyphenol, which are synthesized by 11 genera of Basidiomycetes.The biosynthesis of these chlor...

  18. Chlorine gas exposure increases susceptibility to invasive lung fungal infection

    OpenAIRE

    Gessner, Melissa A.; Doran, Stephen F.; Yu, Zhihong; Dunaway, Chad W.; Matalon, Sadis; Steele, Chad

    2013-01-01

    Chlorine (Cl2) is a highly irritating and reactive gas with potential occupational and environmental hazards. Acute exposure to Cl2 induces severe epithelial damage, airway hyperreactivity, impaired alveolar fluid clearance, and pulmonary edema in the presence of heightened inflammation and significant neutrophil accumulation in the lungs. Herein, we investigated whether Cl2 exposure affected the lung antimicrobial immune response leading to increased susceptibility to opportunistic infection...

  19. Natural chlorine and fluorine in the atmosphere, water and precipitation

    Science.gov (United States)

    Friend, James P.

    1990-01-01

    The geochemical cycles of chlorine and fluorine are surveyed and summarized as framework for the understanding of the global natural abundances of these species in the atmosphere, water, and precipitation. In the cycles the fluxes into and out of the atmosphere can be balanced within the limits of our knowledge of the natural sources and sinks. Sea salt from the ocean surfaces represent the predominant portion of the source of chlorine. It is also an important source of atmospheric fluorine, but volcanoes are likely to be more important fluorine sources. Dry deposition of sea salt returns about 85 percent of the salt released there. Precipitation removes the remainder. Most of the sea salt materials are considered to be cyclic, moving through sea spray over the oceans and either directly back to the oceans or deposited dry and in precipitation on land, whence it runs off into rivers and streams and returns to the oceans. Most of the natural chlorine in the atmosphere is in the form of particulate chloride ion with lesser amounts as gaseous inorganic chloride and methyl chloride vapor. Fluorine is emitted from volcanoes primarily as HF. It is possible that HF may be released directly form the ocean surface but this has not been confirmed by observation. HCl and most likely HF gases are released into the atmosphere by sea salt aerosols. The mechanism for the release is likely to be the provision of protons from the so-called excess sulfate and HNO3. Sea salt aerosol contains fluorine as F(-), MgF(+), CaF(+), and NaF. The concentrations of the various species of chlorine and fluorine that characterize primarily natural, unpolluted atmospheres are summarized in tables and are discussed in relation to their fluxes through the geochemical cycle.

  20. Chlorine decay under steady and unsteady-state hydraulic conditions

    DEFF Research Database (Denmark)

    Stoianov, Ivan; Aisopou, Angeliki

    2014-01-01

    This paper describes a simulation framework for the scale-adaptive hydraulic and chlorine decay modelling under steady and unsteady-state flows. Bulk flow and pipe wall reaction coefficients are replaced with steady and unsteady-state reaction coefficients. An unsteady decay coefficient is defined...... and these demonstrate that the dynamic hydraulic conditions have a significant impact on water quality deterioration and the rapid loss of disinfectant residual. © 2013 The Authors....

  1. Evaluation of low-chlorine TATB from a production source

    Energy Technology Data Exchange (ETDEWEB)

    Stallings, T.L.; Osborn, A.G.; Johnson, H.D.; Duncan, A.A.; Schaffer, C.L.

    1981-08-01

    Six production lots of low-chlorine TATB powder have been evaluated. Five of the lots were made by a wet-amination process and the other was made by an emulsion-amination process. LX-17 physical properties specimens made from the five wet-aminated TATB lots were exceptionally strong and comparable to dry-aminated TATB, while the emulsion-aminated lot of TATB had lower strength.

  2. The influence of chlorine on the gasification of wood

    Energy Technology Data Exchange (ETDEWEB)

    Scala, C. von; Struis, R.; Stucki, S. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

    1997-06-01

    Chlorides of the heavy metals copper, lead and zinc inhibit the CO{sub 2}-gasification reaction of charcoal. This is observed either by impregnation the wood with the salts before pyrolysis or by mechanically mixing the salts with the charcoal before gasification. Charcoal impregnated or mixed with ammonium chloride reacts more slowly than untreated charcoal. Treating the charcoal with HCl also influences negatively the gasification reactivity, indicating that chlorine plays an important role in the gasification. (author) 2 figs., 4 refs.

  3. pH control for enhanced reductive bioremediation of chlorinated solvent source zones

    International Nuclear Information System (INIS)

    Enhanced reductive dehalogenation is an attractive treatment technology for in situ remediation of chlorinated solvent DNAPL source areas. Reductive dehalogenation is an acid-forming process with hydrochloric acid and also organic acids from fermentation of the electron donors typically building up in the source zone during remediation. This can lead to groundwater acidification thereby inhibiting the activity of dehalogenating microorganisms. Where the soils' natural buffering capacity is likely to be exceeded, the addition of an external source of alkalinity is needed to ensure sustained dehalogenation. To assist in the design of bioremediation systems, an abiotic geochemical model was developed to provide insight into the processes influencing the groundwater acidity as dehalogenation proceeds, and to predict the amount of bicarbonate required to maintain the pH at a suitable level for dehalogenating bacteria (i.e., > 6.5). The model accounts for the amount of chlorinated solvent degraded, site water chemistry, electron donor, alternative terminal electron-accepting processes, gas release and soil mineralogy. While calcite and iron oxides were shown to be the key minerals influencing the soil's buffering capacity, for the extensive dehalogenation likely to occur in a DNAPL source zone, significant bicarbonate addition may be necessary even in soils that are naturally well buffered. Results indicated that the bicarbonate requirement strongly depends on the electron donor used and availability of competing electron acceptors (e.g., sulfate, iron (III)). Based on understanding gained from this model, a simplified model was developed for calculating a preliminary design estimate of the bicarbonate addition required to control the pH for user-specified operating conditions.

  4. Kinetics of corrosion of Si3N4 and SiC-Si3N4 composite in oxygen/chlorine environments

    International Nuclear Information System (INIS)

    The kinetics of corrosion of silicon nitride and nitride bonded silicon carbide materials in flowing gas mixtures consisting of argon, oxygen and chlorine was investigated by thermogravimetric analysis. The corrosion process was characterized by two categories; one is volatilization type of attack in which the corrosion proceeds primarily by a formation of volatile corrosion product in low ratio of oxygen to chlorine environments between 900 C and 1100 C. Another is bubble formation type of corrosion in which the reaction proceeds with a small increase in weight due to the formation of bubble in oxide layer in high ratio of oxygen to chlorine environments at 1200 C and 1300 C. Examination of the corroded specimens by scanning electron microscopy, X-ray analysis and transmission electron microscopy indicated that the SiC was selectively attacked in the nitride bonded materials and that in general, the silicon nitride was more resistant to attack than the silicon carbide under mixed oxidation condition. This may be related to the nature of the silicon dioxide films on the two materials because the stability of silicon dioxide becomes a key to whether or not further attack may occur

  5. Chlorine Analysis by Diode Laser Atomic Absorption Spectrometry

    Institute of Scientific and Technical Information of China (English)

    Joachim Koch; Aleksandr Zybin; Kay Niemax

    2000-01-01

    The general characteristics of Diode Laser Absorption Spectrometry (DLAAS) in low pressure plasmas particulary with respect to the detection of non-metals are comprehensively recapitulated and discussed. Furthermore, a detector, which is based on DLAAS in a microwave-induced low pressure plasma as an alternative technique for halogene-specific analysis of volatile compounds and polymeric matrices is described. The analytical capability of the technique is demonstrated on the chlorine-specific analysis of ablated polymer fragments as well as gas chromatographically separated hydrocarbons. Since the measurements were carried out by means of a balanced-heterodyne detection scheme, different technical noise contributions, such as laser excess and RAM noise could efficiently be suppressed and the registered absorption was limited only by the principal shot noise. Thus, in the case of the polymer analysis a chlorine-specific absolute detection limit of 10 pg could be achieved. Furthermore, fundamental investigations concerning the influence of hydrocarbons on the dissociation capability of the microwave induced plasma were performed. For this purpose, the carbon-, chlorine-and hydrogen-specific stoichiometry of the compounds were empirically determined. Deviations from the exspected proportions were found to be insignificant, implying the possibility of internal standardization relative to the response of a reference sample.

  6. Rapid infrared determination of the potency of chlorinated bactericides.

    Science.gov (United States)

    Spagnolo, F; Cestaro, J P

    1971-06-01

    A rapid infrared reflectance method for evaluating the germicidal potency of synthetic materials containing various amounts of two chlorinated bactericides was developed. The dimeric product 2,2'-methylenebis (4,6-dichlorophenol) exhibited a characteristic C=C skeletal inplane stretching infrared absorption band at 1,640 cm(-1). The monomeric 2,4-dichlorophenol precursor showed a characteristic absorption band at 1,579 cm(-1). These characteristic infrared absorptions may be used for analysis of the potency of the manufactured chlorinated bactericide. For a series of samples known to vary in dimer content, the micrograms per milliliter required for a 100% bacterial kill is first determined by a standard American Petroleum Institute method. Then the area ratio of the infrared absorption bands characteristic of the chlorinated bactericides is measured for each sample and plotted versus the microgram per milliliter required for 100% bacterial kill. The potency of subsequent samples is simply and rapidly determined by measuring this ratio from the infrared absorption curve and calculating micrograms per milliliter required for 100% kill from the calibration curve. Analysis time is approximately 1 hr compared to biocidal tests in current use requiring approximately a 1-month incubation period. PMID:5564677

  7. Behavior and control of chlorine in dyestuff residue incineration

    Institute of Scientific and Technical Information of China (English)

    YAN Jian-hua; TAN Zhong-xin; JIANG Xue-guang; CHI Yong; CEN Ke-fa

    2006-01-01

    Dyestuff residue, a type of hazardous waste, is incinerated in the tubular furnace, and thermodynamic equilibrium model is used to calculate and analyze the chlorine behavior. The HCl emission and its effects on the behaviors of heavy metals are studied.Meanwhile, the effects of three dechlorine reagents are predicted at a high temperature. Results show that HCl emission is dependent on incineration temperature. The HCl evaporated mainly derives from the organic chlorine. Under the working condition of 500--900℃, the main products of Hg, Pb, Cu, Ni, Zn, and Mn in reaction with HCl are HgCl2 (g), PbCl4(g), PbCl2 (g), (CuCl)3 (g), NiCl2 (s),NiCl2 (g), ZnCl2 (s), ZnCl2 (g), Zn (g), MnCl2 (s), and MnCl2 (g), respectively. Among the three dechlorine reagents, CaCO3 is optimal to remove chlorine at high temperature, little of HCl is released below 800℃, whereas Fe3O4 is unstable at high temperature.

  8. Depletion of chlorine into HCl ice in a protostellar core

    CERN Document Server

    Kama, M; Lopez-Sepulcre, A; Wakelam, V; Dominik, C; Ceccarelli, C; Lanza, M; Lique, F; Ochsendorf, B B; Lis, D C; Caballero, R N; Tielens, A G G M

    2014-01-01

    The freezeout of gas-phase species onto cold dust grains can drastically alter the chemistry and the heating-cooling balance of protostellar material. In contrast to well-known species such as carbon monoxide (CO), the freezeout of various carriers of elements with abundances $<10^{-5}$ has not yet been well studied. Our aim here is to study the depletion of chlorine in the protostellar core, OMC-2 FIR 4. We observed transitions of HCl and H2Cl+ towards OMC-2 FIR 4 using the Herschel Space Observatory and Caltech Submillimeter Observatory facilities. Our analysis makes use of state of the art chlorine gas-grain chemical models and newly calculated HCl-H$_{2}$ hyperfine collisional excitation rate coefficients. A narrow emission component in the HCl lines traces the extended envelope, and a broad one traces a more compact central region. The gas-phase HCl abundance in FIR 4 is 9e-11, a factor of only 0.001 that of volatile elemental chlorine. The H2Cl+ lines are detected in absorption and trace a tenuous fo...

  9. SOME ASPECTS REGARING CHLORINE DECAY IN WATER DISTRIBUTION NETWORKS

    Directory of Open Access Journals (Sweden)

    LIANA IOANA VUŢĂ

    2011-03-01

    Full Text Available A major objective of drinking water treatment is to provide microbiologically safe drinking water. The combination of conventional drinking water treatment and disinfection has proved to be one of the major public health advances in modern times. The quality of drinking water delivered to the customer’s tap is influenced by a number of processes; namely water treatment, disinfection and changes during transport of treated water via the distribution system. All natural waters and even treated drinking water exerts disinfectant demand due to the reactions with NOM and other constituents in water. Therefore, the applied disinfectant dose must be sufficient to meet the inherent demand in the treated water, to provide sufficient protection against microbial infection. Thus, controlling free residual chlorine properly is definitely important to ensure meeting regulatory requirements and satisfying customer needs.This paper presents the main aspects regarding chlorine decay in drinking-water distribution networks and, also a free chlorine decay simulation with EPANET2 on Ramnicu Valcea water distribution system.

  10. Impact of January 2005 solar proton events on chlorine species

    Directory of Open Access Journals (Sweden)

    A. Damiani

    2012-05-01

    Full Text Available Sudden changes in stratospheric chlorine species in the polar northern atmosphere, caused by the Solar Proton Events (SPEs of 17 and 20 January 2005, have been investigated and compared with version 4 of the Whole Atmosphere Community Climate Model (WACCM4. We used Aura Microwave Limb Sounder (MLS measurements to monitor the variability of ClO, HCl, HOCl and Michelson Interferometer for Passive Atmospheric Sounder (MIPAS on ENVISAT to retrieve ClONO2. SPE-induced chlorine activation has been identified. HCl decrease occurred at nearly all the investigated altitudes (i.e., 10–0.5 hPa with the strongest decrease (of about 0.25 ppbv on 21 January. HOCl was found to be the main active chlorine species under nighttime conditions (with increases of more than 0.2 ppbv whereas both HOCl and ClO enhancements (about 0.1 ppbv have been observed at the polar night terminator. Further, small ClO decreases (of less than 0.1 ppbv and ClONO2 enhancements (about 0.2 ppbv have been observed at higher latitudes (i.e., at nighttime roughly above 2 hPa.

    While WACCM4 reproduces most of the SPE-induced variability in the chlorine species fairly well, in some particular regions discrepancies between the modeled and measured temporal evolution of the abundances of chlorine species were found. HOCl changes are modelled very well with respect to both magnitude and geographic distribution. ClO decreases are reproduced at high latitudes, whereas ClO enhancements in the terminator region are underestimated and attributed to background variations. WACCM4 also reproduces the HCl depletion in the mesosphere but it does not show the observed decrease below about 2 hPa. Finally, WACCM4 simulations indicate that the observed ClONO2 increase is dominated by background variability, although SPE-induced production might contribute by 0.1 ppbv.

  11. Resistance and Inactivation Kinetics of Bacterial Strains Isolated from the Non-Chlorinated and Chlorinated Effluents of a WWTP

    Directory of Open Access Journals (Sweden)

    Claudia Coronel-Olivares

    2013-08-01

    Full Text Available The microbiological quality of water from a wastewater treatment plant that uses sodium hypochlorite as a disinfectant was assessed. Mesophilic aerobic bacteria were not removed efficiently. This fact allowed for the isolation of several bacterial strains from the effluents. Molecular identification indicated that the strains were related to Aeromonas hydrophila, Escherichia coli (three strains, Enterobacter cloacae, Kluyvera cryocrescens (three strains, Kluyvera intermedia, Citrobacter freundii (two strains, Bacillus sp. and Enterobacter sp. The first five strains, which were isolated from the non-chlorinated effluent, were used to test resistance to chlorine disinfection using three sets of variables: disinfectant concentration (8, 20 and 30 mg·L−1, contact time (0, 15 and 30 min and water temperature (20, 25 and 30 °C. The results demonstrated that the strains have independent responses to experimental conditions and that the most efficient treatment was an 8 mg·L−1 dose of disinfectant at a temperature of 20 °C for 30 min. The other eight strains, which were isolated from the chlorinated effluent, were used to analyze inactivation kinetics using the disinfectant at a dose of 15 mg·L−1 with various retention times (0, 10, 20, 30, 60 and 90 min. The results indicated that during the inactivation process, there was no relationship between removal percentage and retention time and that the strains have no common response to the treatments.

  12. Oxidation of Ketones: A (Chemo-) Enzymatic Approach Using Oxygenases and Hydrolases

    OpenAIRE

    Chávez, Georgina

    2013-01-01

    Oxidation reactions are important in organic chemistry as well as in nature. In industry, oxidations are commonly used for the synthesis of chemicals and pharmaceuticals, however such processes have a number of limitations, they use chlorinated solvents, stoichiometric oxidation reagents, and in some cases the reagents that have risks of explosion during transportation and storage. This has called for more environment-friendly alternative technologies for oxidation reactions. Baeyer-Villiger ...

  13. Research of chemical induction unit on mixing effect and chlorine saving

    Institute of Scientific and Technical Information of China (English)

    Jiao Zhongzhi; Chen Zhonglin; Li ZuoLiang; Xue Zhu; Yuan Xing; Li Guibai

    2007-01-01

    Rapid mixing and chlorine saving are two important problems that most drinking water industries ale focus on, and this paper adopts chemical induction unit to compare with water jet injector to study what merits chemical induction unit has. The experiment chose coefficient of variability of chlorine concentration to evaluate the mix effect and used chlorine consumption to compare the two equipments. Distribution reservoir experiments show that chemical induction unit can completely mix chlorine less than 6. 2 seconds and water jet injector can not completely mix in 3 minutes. Mixing pool experiments show that chemical induction unit can save chlorine compared with water jet injector, and Can save mole if mole chlorine is consumed.

  14. SIMULTANEOUS DETERMINATION OF CHLORINE DIOXIDE AND HYPOCHLOROUS ACID IN BLEACHING SYSTEM

    Directory of Open Access Journals (Sweden)

    Qiang Wang

    2011-04-01

    Full Text Available This study has demonstrated a rapid spectroscopic method for the determination of chlorine dioxide and hypochlorous acid concentrations in the pulp bleaching processes. It was found that chlorine dioxide and hypochlorous acid have an isosbestic wavelength of 295 nm. The soluble lignin in such a system is the main interference, but can be corrected by determining the absorbances at 295 nm, 380 nm, and 480 nm. Thus, based on the spectroscopic measurements at 295 nm (the isosbestic point wavelength for chlorine dioxide and hypochlorous acid, 380 nm (absorbance wavelength of chlorine dioxide and 480 nm (the acid soluble lignin absorbance wavelength, the chlorine dioxide and hypochlorous acid concentrations in the bleaching process can be quantified. However, hypochlorous acid was not detected in the real bleaching effluent for its low content. The present method is simple, rapid, accurate, and has the potential for on-line monitoring of the chlorine dioxide bleaching process.

  15. The role of bound chlorine in the brightness reversion of bleached hardwood kraft pulp

    OpenAIRE

    Kátia Maria Morais Eiras; Jorge Luiz Colodette; Vanessa Lopes Silva

    2009-01-01

    Our previous paper showed fragmentary evidence that pulp brightness reversion may be negatively affected by its organically bound chlorine (OX) content. A thorough investigation on eucalyptus kraft pulp led to the conclusion that OX increases reversion of certain pulps but this trend is not universal. Alkaline bleaching stages decrease reversion regardless of pulp OX content. Pulps bleached with high temperature chlorine dioxide revert less than those bleached with conventional chlorine dioxi...

  16. Use of integrated cell culture-PCR to evaluate the effectiveness of poliovirus inactivation by chlorine.

    Science.gov (United States)

    Blackmer, F; Reynolds, K A; Gerba, C P; Pepper, I L

    2000-05-01

    Current standards, based on cell culture assay, indicate that poliovirus is inactivated by 0.5 mg of free chlorine per liter after 2 min; however, integrated cell culture-PCR detected viruses for up to 8 min of exposure to the same chlorine concentration, requiring 10 min for complete inactivation. Thus, the contact time for chlorine disinfection of poliovirus is up to five times greater than previously thought.

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

    OpenAIRE

    Grabeel, Margaret N.

    1992-01-01

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

  18. Synergistic prevention of biofouling in seawater desalination by zwitterionic surfaces and low-level chlorination.

    Science.gov (United States)

    Yang, Rong; Jang, Hongchul; Stocker, Roman; Gleason, Karen K

    2014-03-19

    Smooth, durable, ultrathin antifouling layers are deposited onto commercial reverse osmosis membranes without damaging them and they exhibit a fouling reduction. A new synergistic approach to antifouling, by coupling surface modification and drinking-water-level chlorination is enabled by the films' unique resistance against chlorine degradation. This approach substantially enhances longer-term fouling resistance compared with surface modification or chlorination alone, and can reduce freshwater production cost and its collateral toxicity to marine biota.

  19. Synthesis and chlorination of manganese-columbine by means of a solid-gas reaction. Determination of crystalline structures

    International Nuclear Information System (INIS)

    Full text. The synthesis of mangano-columbite was carried out as follows: Mixing of N B 203 and Mn Cl 2 with an 10% weight excess of the latter in order to compensate for losses due to volatilization; grinding of the mixture in an agate mortar with agate handle in order to achieve close contact between the two solids; calcination of the sample in a quartz crucible at temperatures between 610 and 620 C (fusion temperature for Mn Cl2) in N2 current for six hours. After this time, temperature was increased at a eat of 50 C/h until reaching 800 C. This temperature was maintained for two hours in order to eliminate Mn Cl2 excess; cooling of the obtained product in N2 current. XRD analysis showed that the obtained products is a mangano-columbite. The mineral in natural state presents and orthorhombic structure. The structure of the synthesized product, though corresponding to mangano-columbite according to DRX, should be confirmed by means of an additional technique such as EXAFS. Th mangano-columbite obtained was subsequently chlorinated at 900 deg C for two hours to obtain conversions close to 50%, at 101 kPa, with a chlorine molar fraction of 1 and a flow of 50 cm3/min. By XRD it can be observed that the chlorination residue presents unreacted mangano-columbite and niobium oxide in an unknown phase, whose crystalline structure is currently under study. Measurements to be performed by means Synchrotron Radiation (EXAFS and XANES) might help elucidate this new structure. (author)

  20. The role of bound chlorine in the brightness reversion of bleached hardwood kraft pulp

    Directory of Open Access Journals (Sweden)

    Kátia Maria Morais Eiras

    2009-01-01

    Full Text Available Our previous paper showed fragmentary evidence that pulp brightness reversion may be negatively affected by its organically bound chlorine (OX content. A thorough investigation on eucalyptus kraft pulp led to the conclusion that OX increases reversion of certain pulps but this trend is not universal. Alkaline bleaching stages decrease reversion regardless of pulp OX content. Pulps bleached with high temperature chlorine dioxide revert less than those bleached with conventional chlorine dioxide in sequences ending with a chlorine dioxide stage but similarly in sequences ending with a final peroxide stage. The use of secondary condensate for pulp washing decreases reversion.

  1. Safety and environmental aspects of zinc--chlorine hydrate batteries for electric-vehicle applications

    Energy Technology Data Exchange (ETDEWEB)

    Kodali, S.; Henriksen, G.L.; Whittlesey, C.C.; Warde, C.J.; Carr, P.; Symons, P.C.

    1978-03-01

    Public acceptance of high-performance cost-effective zinc--chlorine hydrate batteries for the random-use electric-vehicle application will require meeting stringent safety and environmental requirements. These requirements revolve mainly around the question of accidental release and spread of toxic amounts of chlorine gas, the only potential hazard in this battery system. Available information in the areas of physiological effects, environmental impact, and governmental regulation of chlorine were reviewed. The design, operation, and safety features of a first commercial electric-vehicle battery were conceived and analyzed from the chlorine release aspect. Two types of accident scenarios were analyzed in terms of chlorine release rates, atmospheric dispersion, health hazard, and possible clean-up operations. The worst-case scenario, a quite improbable accident, involves the spillage of chlorine hydrate onto the ground, while the other scenario, a more probable accident, involves the release of chlorine gas from a ruptured battery case. Heat-transfer and chlorine-dispersion models, developed to analyze these scenarios, establish a firm basis for a comprehenive and factual position statement on this topic. The results of this preliminary study suggest that electric vehicles powered by appropriately designed zinc--chlorine hydrate batteries will pose negligible health or environmental hazards on the nation's streets and highways. 8 figures, 14 tables.

  2. Oak Ridge K-25 Site chlorinated solvent pollution prevention opportunity assessment

    International Nuclear Information System (INIS)

    A pollution prevention opportunity assessment (PPOA) was conducted at the Oak Ridge K-25 Site to identify opportunities to reduce and better manage the use of chlorinated solvents. At the K-25 Site, 67 control areas were examined for their potential use of chlorinated solvents. Of these areas, 27 were found to be using (1) chlorinated solvents for cleaning, degreasing, and lubricating; (2) laboratory standards and solvents; and (3) test medium. Current management practices encourage the identification and use of nonhazardous chemicals, including the use of chlorinated solvents. The main pollution prevention principles are source reduction and recycling, and a number of pollution prevention options based on these principles were identified and evaluated as part of this chlorinated solvent PPOA. Source reduction options evaluated for the K-25 Site include the substitution of chlorinated solvents with nonchlorinated solvents. Recycling was identified for those areas that would benefit most from the reuse of the chlorinated solvents in use. The pollution prevention options that offer the greatest opportunity for success at the K-25 Site are the implementation of substitutes at the 10 control areas using chlorinated solvents for cleaning, degreasing, and lubrication. A change in the process may be all that is needed to eliminate the use of a chlorinated solvent. Once a decision is made to implement a substitution, the information should be communicated to all shops and laboratories. Another option to consider is the installation of recycling units to recycle the large amounts of methylene chloride used in the analytical sampling procedure

  3. 二氧化氯去除污染物及其动力学研究进展%Research Progress on Kinetics of PoUutants Removal by Chlorine Dioxide

    Institute of Scientific and Technical Information of China (English)

    曹向禹

    2012-01-01

    二氧化氯在消毒杀菌、饮用水净化、工业废水处理和纸浆漂白等领域的应用广泛,是一种极具潜力的绿色氧化剂。本文介绍目前国内外二氧化氯对无机和有机污染物去除的研究现状,并对二氧化氯氧化水中污染物反应动力学的研究进展进行了全面综述,为二氧化氯的应用提供理论指导。%Chlorine dioxide, as a potential green oxidant, is increasingly be used in disinfection, drinking water puritication, industrial wastewater treatment and pulp bleaching process. In the paper, the current research situations of chlorine dioxide in both organic and inorganic pollutants removal were introduced. The internal and external research progress on oxidation kinetics of pollutants in water by chlorine dioxide is summarized comprehensively, which can provide theoretical instruction for application of chlorine dioxide in the furore.

  4. Zirconium oxide obtainment from brazilian zircon concentrate

    International Nuclear Information System (INIS)

    This work presents the experimental results of studies about alkaline melting, acid leaching and sulfation steps for obtention of zirconium oxide and partially stabilized zirconia by yttrium and rare-earth coprecipitation in chlorine medium, starting from the brazilian zircon concentrate. Using statistical methods of factorial design and the Packett-Burman approach, the results are discussed and the optimal conditions of the production steps were determined. (author)

  5. Activated Persulfate Treatment of 1,4-Dioxane in the Presence of Chlorinated Solvent Co-contaminants

    Science.gov (United States)

    Boving, T. T.; Eberle, D. E. H.; Ball, R.

    2014-12-01

    1,4-dioxane is an emerging groundwater contaminant and a likely human carcinogen. Due to its history as a stabilizer in chlorinated solvents, 1,4-dioxane is often found as a co-contaminant at solvent releases sites such as landfills, solvent recycling facilities, vapor decreasing operations, and fire-training areas. Historically, 1,4-dioxane was not routinely analyzed for at solvent release sites. The lack of analyses and the limitations of the analyses that were performed (i.e. high reporting limits) means that the scale of 1,4-dioxane subsurface contamination is still emerging. With the number of known 1,4-dioxane sites increasing, the need for cost effective 1,4-dioxane remediation technologies is rising as well. Remediation strategies that are capable of treating both 1,4-dioxane as well as chlorinated co-contaminants are of particular importance, especially when treating mixed-waste source zones. In the present study, we examined the fate of 1,4-dioxane during the targeted remediation of aqueous phase volatile organic compounds (VOC) using an activated persulfate based ISCO method (OxyZone®). Bench scale laboratory experiments are used to evaluate the treatability of 1,4-dioxane both as a single compound and in the presence of trichloroethene (TCE) and 1,1,1-trichloroethane (1,1,1-TCA). Possible dependencies on oxidant concentration and reaction kinetics were studied. Preliminary results are promising and show that OxyZone® is persistent and long lived, with oxidation of 1,4-dioxane continuing more than 12 days after initial dosage, even at dilute oxidant concentrations. The oxidative destruction of 1,4-dioxane, TCE and 1,1,1-TCA in single compound batch systems followed pseudo first order reaction kinetics. The rate of oxidation for each contaminant increased linearly with increasing persulfate concentration over the range of oxidant concentrations tested. The rate of oxidative destruction, from most easily degraded to least was: TCE > 1,4-Dioxane > 1

  6. Copper chloride electrolyzer for the production of hydrogen via the copper-chlorine thermochemical cycle

    Science.gov (United States)

    Roy, Rahul Dev

    Hydrogen is considered a key element in solving the upcoming energy crisis, it is not the primary fuel source but an "energy carrier" similar to electricity and has to be produced using some other hydrogen rich source. Thermochemical water decomposition is a promising alternative to steam-methane reforming and electrolytic water splitting for a sustainable method of large-scale hydrogen production. The Copper-Chlorine thermochemical cycle is one of prime contenders among all the other thermochemical cycles being studied because of its low energy requirements compared to others and mild operating conditions, therefore making it available to be readily integrated to the available nuclear reactors or solar energy installations. This present work focuses on the study and development of a proton exchange membrane (PEM) electrolyzer cell for the Copper-Chlorine thermo chemical cycle to obtain a better understanding through experiments and models of this process. Different operating and design parameters such as temperature, flow rate, current density, membranes and gas diffusion layers were considered to reduce the voltage and hence increase the efficiency of the electrolyzer. The effects of catalyst and mass transfer were studied on the thin film electrode using a rotating disk electrode (RDE) setup. A mathematical model was also developed to monitor the performance of the electrolyzer by predicting the change in concentration of copper chloride in the system with respect to time. It is observed that flow rate and temperature plays a major role in decreasing the voltage drop. There was no effect of catalyst in the anode when compared to a bare anode at lower flow rates; but at higher flow rates there was significant decrease in voltage drop when a carbon cloth was placed at the anode end. High surface area carbon black has comparable activity towards CuCl oxidation with conventional catalyst like Platinum or Ruthenium oxide. It is also seen that mass transfers possess a

  7. Suppression of chlorine activation on aviation-produced volatile particles

    Directory of Open Access Journals (Sweden)

    S. K. Meilinger

    2002-07-01

    Full Text Available We examine the effect of nm-sized aircraft-induced aqueous sulfuric acid (H2SO4/H2O particles on atmospheric ozone as a function of temperature. Our calculations are based on a previously derived parameterization for the regional-scale perturbations of the sulfate surface area density due to air traffic in the North Atlantic Flight Corridor (NAFC and a chemical box model. We confirm large scale model results that at temperatures T > 210 K additional ozone loss -- mainly caused by hydrolysis of BrONO2 and N2O5 -- scales in proportion with the aviation-produced increase of the background aerosol surface area. However, at lower temperatures (< 210 K we isolate two effects which efficiently reduce the aircraft-induced perturbation: (1 background particles growth due to H2O and HNO3 uptake enhance scavenging losses of aviation-produced liquid particles and (2 the Kelvin effect efficiently limits chlorine activation on the small aircraft-induced droplets by reducing the solubility of chemically reacting species. These two effects lead to a substantial reduction of heterogeneous chemistry on aircraft-induced volatile aerosols under cold conditions. In contrast we find contrail ice particles to be potentially important for heterogeneous chlorine activation and ozone depletion. These features have not been taken into consideration in previous global studies of the atmospheric impact of aviation. Therefore, to parameterize them in global chemistry and transport models, we propose the following parameterisation: scale the hydrolysis reactions by the aircraft-induced surface area increase, and neglect heterogeneous chlorine reactions on liquid plume particles but not on ice contrails and aircraft induced ice clouds.

  8. Suppression of chlorine activation on aviation-produced volatile particles

    Directory of Open Access Journals (Sweden)

    S. K. Meilinger

    2002-01-01

    Full Text Available We examine the effect of nanometer-sized aircraft-induced aqueous sulfuric acid (H2SO4/H2O particles on atmospheric ozone as a function of temperature. Our calculations are based on a previously derived parameterization for the regional-scale perturbations of the sulfate surface area density due to air traffic in the North Atlantic Flight Corridor (NAFC and a chemical box model. We confirm large scale model results that at temperatures T>210 K additional ozone loss -- mainly caused by hydrolysis of BrONO2 and N2O5 -- scales in proportion with the aviation-produced increase of the background aerosol surface area. However, at lower temperatures (2O and HNO3 uptake enhance scavenging losses of aviation-produced liquid particles and (2 the Kelvin effect efficiently limits chlorine activation on the small aircraft-induced droplets by reducing the solubility of chemically reacting species. These two effects lead to a substantial reduction of heterogeneous chemistry on aircraft-induced volatile aerosols under cold conditions. In contrast we find contrail ice particles to be potentially important for heterogeneous chlorine activation and reductions in ozone levels. These features have not been taken into consideration in previous global studies of the atmospheric impact of aviation. Therefore, to parameterize them in global chemistry and transport models, we propose the following parameterisation: scale the hydrolysis reactions by the aircraft-induced surface area increase, and neglect heterogeneous chlorine reactions on liquid plume particles but not on ice contrails and aircraft induced ice clouds.

  9. Modeling Penicillium expansum resistance to thermal and chlorine treatments.

    Science.gov (United States)

    Salomão, Beatriz C M; Churey, John J; Aragão, Gláucia M F; Worobo, Randy W

    2009-12-01

    Apples and apple products are excellent substrates for Penicillium expansum to produce patulin. In an attempt to avoid excessive levels of patulin, limiting or reducing P. expansum contamination levels on apples designated for storage in packinghouses and/or during apple juice processing is critical. The aim of this work was (i) to determine the thermal resistance of P. expansum spores in apple juice, comparing the abilities of the Bigelow and Weibull models to describe the survival curves and (ii) to determine the inactivation of P. expansum spores in aqueous chlorine solutions at varying concentrations of chlorine solutions, comparing the abilities of the biphasic and Weibull models to fit the survival curves. The results showed that the Bigelow and Weibull models were similar for describing the heat inactivation data, because the survival curves were almost linear. In this case, the concept of D- and z-values could be used, and the D-values obtained were 10.68, 6.64, 3.32, 1.14, and 0.61 min at 50, 52, 54, 56, and 60 degrees C, respectively, while the z-value was determined to be 7.57 degrees C. For the chlorine treatments, although the biphasic model gave a slightly superior performance, the Weibull model was selected, considering the parsimony principle, because it has fewer parameters than the biphasic model has. In conclusion, the typical pasteurization regimen used for refrigerated apple juice (71 degrees C for 6 s) is capable of achieving a 6-log reduction of P. expansum spores.

  10. Transfer of chlorine from the environment to agricultural foodstuffs

    International Nuclear Information System (INIS)

    The factors governing chlorine transfer from Phaeozem and Greyzem soils to various important crop species (foodstuff and forage) were determined in natural conditions in the Kiev region of Ukraine. The stable chlorine concentration ratio (CR) values were the lowest in apple (0.5 ± 0.3) and strawberry (2 ± 1), higher in vegetables (5 ± 3), seeds (15 ± 7) and reached a maximum in straw (187 ± 90). The average CR values of 36Cl were estimated for the most important crops using all experimental data on 36Cl and stable chlorine transfer into plants from various soils. It was experimentally shown that boiling potatoes in water leads to an equilibrium between 36Cl specific content in the water and moisture in the cooked potato. The 36Cl processing factor (PF) for boiling various foodstuffs is equal to the ratio of water mass in the cooked foodstuff to the total water mass (in the food and the decoction). 36Cl PF for cereal flour can be estimated as 1. The 36Cl processing factor for dairy products is equal to the ratio of residual water mass in the product to initial water mass in milk. At a 36Cl specific activity in soil of 1 Bq kg-1, the estimated annual dietary 36Cl intake into human organism (adult man) is about 10 kBq. Sixty to seventy percent of the above amount will be taken in via milk and dairy products, 7-16% via meat, 14-16% via bread and bakery items and 8-12% via vegetables. The highest annual 36Cl intake, 10.7 kBq, is predicted for 1-year-old children. The expected effective doses from annual 36Cl intake are higher for younger age groups, increasing from 0.008 mSv in adults to 0.12 mSv in 1-year-old children

  11. A new formulation of equivalent effective stratospheric chlorine (EESC

    Directory of Open Access Journals (Sweden)

    P. A. Newman

    2007-09-01

    Full Text Available Equivalent effective stratospheric chlorine (EESC is a convenient parameter to quantify the effects of halogens (chlorine and bromine on ozone depletion in the stratosphere. We show, discuss, and analyze a new formulation of EESC that now includes the effects of age-of-air dependent fractional release values and an age-of-air spectrum. This EESC can be more appropriately applied to various parts of the stratosphere because of this dependence on mean age-of-air. This new formulation provides quantitative estimates of EESC that can be directly related to inorganic chlorine and bromine throughout the stratosphere. In this paper, we first provide a detailed description of the EESC calculation. We then use this EESC formulation to estimate that human-produced ozone depleting substances will recover to 1980 levels in 2041 in the midlatitudes, and 2067 over Antarctica. These recovery dates are based upon the assumption that the international agreements for regulating ozone-depleting substances are adhered to. In addition to recovery dates, we also estimate the uncertainties and possible problems in the estimated times of recovery. The midlatitude recovery of 2041 has a 95% confidence uncertainty from 2028 to 2049, while the 2067 Antarctic recovery has a 95% confidence uncertainty from 2056 to 2078. The principal uncertainties are from the estimated mean age-of-air and fractional release values, and the assumption that these quantities are time independent. Using other model estimates of age decrease due to climate change, we estimate that midlatitude recovery may be significantly accelerated.

  12. In situ bioremediation of petroleum hydrocarbons and chlorinated hydrocarbons: Three case studies

    International Nuclear Information System (INIS)

    In situ biodegradation of organic contaminants is one of the most cost-effective means of site remediation. This method has proven successful in soils, ground water, and slurries. Bacteria capable of degrading organic contaminants within an aquifer include many species from a wide spectrum of genera, e.g. Pseudomonas, Corynebacterium, Bacillus, etc. In most cases, a mixture of bacterial strains is required to completely oxidize a complex organic contaminant. Each strain of an organism may target a specific compound, working together with other organisms to ultimately degrade each intermediate until complete degradation, also known as mineralization, occurs. One or more of the following mechanisms are utilized by bacteria for organic chemical degradation: (1) aerobic, (2) anaerobic, and (3) co-metabolic. During aerobic oxidation of organic chemicals, bacteria utilize the pollutant as an electron and hydrogen source and oxygen acts as the electron and hydrogen acceptor, resulting in water. As the bacterial enzymes cleave the compound, oxidized products are produced along with energy for the reaction to proceed. This is the most rapid and widely utilized mechanism. Dehalogenation occurs under aerobic, or perhaps more often, under anoxic conditions. This process occurs in the presence of alternate electron acceptors and replaces chlorine with hydrogen. The mechanism of co-metabolism can be aerobic or anaerobic, but is more often aerobic. This process requires a separate energy source for the bacterial cell because the pollutant is not utilized as an energy source. The role of bioremediation in site remediation is demonstrated below by three case studies: (1) a refinery, (2) a municipal landfill and (3) a pesticide formulation plant

  13. Oxidation of dithiocarbamates to yield N-nitrosamines by water disinfection oxidants.

    Science.gov (United States)

    Padhye, Lokesh P; Kim, Jae-Hong; Huang, Ching-Hua

    2013-02-01

    Two most commonly used dithiocarbamate (DTC) pesticides, dimethyldithiocarbamate (DMDTC) and diethyldithiocarbamate (DEDTC), were examined in this study to evaluate their potential to form nitrosamines when in contact with various water disinfection oxidants. Results show that DTCs can serve as nitrosamine precursors, by release of secondary amines through hydrolysis or through reactions with oxidants. The reactions of DTCs with monochloramine and ozone were found to be particularly problematic in the risk of generating nitrosamines, though all four tested oxidants, including free chlorine and chlorine dioxide, formed nitrosamines. NDEA yield from DEDTC was lower, by different degrees, than NDMA yield from DMDTC for all four oxidants, which was attributed to the steric hindrance associated with bulkier reaction intermediate that are more difficult to be further oxidized to form nitrosamine. The yield of nitrosamines increased with the oxidant dosage for both monochloramination and ozonation of DTCs. Results for nitrosamine formation from DTCs at varying pH were found to be consistent with the pH trend of nitrosamine formation from ozonation and monochloramination of secondary amines. Kinetic study results and identification and quantification of reaction products suggest that the DTCs were not significant direct precursors of nitrosamines during monochloramination or ozonation, but rather nitrosamines formed were primarily from reaction of oxidants with the amine which may be generated either through hydrolysis or through oxidation of DTCs. PMID:23176828

  14. BEAM-FOIL SPECTROSCOPY OF CHLORINE AND SULFUR IONS

    OpenAIRE

    Frot, D.; Barchewitz, R.; Cukier, M.; Dei-Cas, R.; Bruneau, J

    1987-01-01

    We report on the measurement of spectra of highly stripped chlorine and sulfur ions in the energy ranges of, respectively, 2900 - 3500 eV and 2300 - 2600 eV. The spectra have been obtained after excitation of ions travelling through a thin carbon foil . X-rays emitted by the emerging beam are analyzed with a Johanntype bent crystal spectrometer. The observation angle with respect to the beam axis is 54°. The interpretation of the spectra is performed by comparing experimental results with Mul...

  15. Future chlorine-bromine loading and ozone depletion

    Science.gov (United States)

    Prather, Michael J.; Ibrahim, Abdel Moneim; Sasaki, Toru; Stordal, Frode; Visconti, Guido

    1991-01-01

    The prediction of future ozone requires three elements: (1) a scenario for the net emissions of chemically and radiatively active trace gases from the land and oceans; (2) a global atmospheric model that projects the accumulation of these gases; and (3) a chemical transport model that describes the distribution of ozone for a prescribed atmospheric composition and climate. This chapter, of necessity, presents models for all three elements and focuses on the following: (1) atmospheric abundance of chlorine and bromine in the form of halocarbons; and (2) the associated perturbations to stratospheric ozone.

  16. Chlorine-based plasma etching of GaN

    Energy Technology Data Exchange (ETDEWEB)

    Shul, R.J.; Briggs, R.D. [Sandia National Labs., Albuquerque, NM (United States); Pearton, S.J.; Vartuli, C.B.; Abernathy, C.R.; Lee, J.W. [Univ. of Florida, Gainesville, FL (United States). Dept. of Materials Science and Engineering; Constantine, C.; Baratt, C. [Plasma-Therm, Inc., Saint Petersburg, FL (United States)

    1997-02-01

    The wide band gap group-III nitride materials continue to generate interest in the semiconductor community with the fabrication of green, blue, and ultraviolet light emitting diodes (LEDs), blue lasers, and high temperature transistors. Realization of more advanced devices requires pattern transfer processes which are well controlled, smooth, highly anisotropic and have etch rates exceeding 0.5 {micro}m/min. The utilization of high-density chlorine-based plasmas including electron cyclotron resonance (ECR) and inductively coupled plasma (ICP) systems has resulted in improved GaN etch quality over more conventional reactive ion etch (RIE) systems.

  17. Theoretical study of the thermochemistry of chlorine oxyfluorides

    Science.gov (United States)

    Sánchez, Hernán R.; Del Pla, Julián

    2016-10-01

    There is a lack of experimental thermochemical values for most chlorine oxyfluorides. Previous high level theoretical, CCSD(T), results showed uncommonly large errors in the standard heats of formation calculated through the atomization method. We propose that the differences are due to unusually large contributions to energy from higher excitations within the coupled cluster framework, and we tackle the problem by using a calculation scheme based on isodesmic reactions. Our suspicions are supported by results of static correlation diagnostics. Our final recommended values are in better agreement with the experimental data available. Other thermodynamic properties are also calculated.

  18. Native sulfur/chlorine SAD phasing for serial femtosecond crystallography

    Energy Technology Data Exchange (ETDEWEB)

    Nakane, Takanori [The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033 (Japan); Song, Changyong [RIKEN SPring-8 Center, 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5148 (Japan); POSTECH, Pohang 790-784 (Korea, Republic of); Suzuki, Mamoru [RIKEN SPring-8 Center, 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5148 (Japan); Osaka University, 3-2 Yamadaoka, Suita, Osaka 565-0871 (Japan); Nango, Eriko; Kobayashi, Jun [RIKEN SPring-8 Center, 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5148 (Japan); Masuda, Tetsuya [RIKEN SPring-8 Center, 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5148 (Japan); Kyoto University, Gokasho, Uji, Kyoto 611-0011 (Japan); Inoue, Shigeyuki [RIKEN SPring-8 Center, 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5148 (Japan); The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033 (Japan); Mizohata, Eiichi [Department of Applied Chemistry, Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871 (Japan); Nakatsu, Toru [RIKEN SPring-8 Center, 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5148 (Japan); Kyoto University, 46-29 Yoshida Shimoadachi-cho, Sakyo-ku, Kyoto 606-8501 (Japan); Tanaka, Tomoyuki; Tanaka, Rie [RIKEN SPring-8 Center, 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5148 (Japan); Shimamura, Tatsuro [Kyoto University, Yoshidakonoe-cho, Sakyo-ku, Kyoto 606-8501 (Japan); Tono, Kensuke; Joti, Yasumasa; Kameshima, Takashi [Japan Synchrotron Radiation Research Institute, 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5198 (Japan); Hatsui, Takaki; Yabashi, Makina [RIKEN SPring-8 Center, 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5148 (Japan); Nureki, Osamu [The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033 (Japan); Iwata, So [RIKEN SPring-8 Center, 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5148 (Japan); Kyoto University, Yoshidakonoe-cho, Sakyo-ku, Kyoto 606-8501 (Japan); Sugahara, Michihiro, E-mail: msuga@spring8.or.jp [RIKEN SPring-8 Center, 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5148 (Japan)

    2015-11-27

    Sulfur SAD phasing facilitates the structure determination of diverse native proteins using femtosecond X-rays from free-electron lasers via serial femtosecond crystallography. Serial femtosecond crystallography (SFX) allows structures to be determined with minimal radiation damage. However, phasing native crystals in SFX is not very common. Here, the structure determination of native lysozyme from single-wavelength anomalous diffraction (SAD) by utilizing the anomalous signal of sulfur and chlorine at a wavelength of 1.77 Å is successfully demonstrated. This sulfur SAD method can be applied to a wide range of proteins, which will improve the determination of native crystal structures.

  19. Bromination vis-a-vis chlorination as a biocide feasibility study

    International Nuclear Information System (INIS)

    Water is used extensively as a cooling medium in various heat transfer equipment's of a power industry such as condenser, heat exchangers and cooling towers. At elevated temperature, the breeding of microbiological growth can form slimes, underneath of this, accelerated corrosion can take place resulting into sudden and catastrophic failure of equipment's. The microbiological growth unchecked in the various systems especially in low velocity areas can lead to large growth of micro organisms such as algae which can even reduce the flow of the fluid thus affecting the efficiency of plant equipment's. Therefore, chlorination is a mandatory requirement in industrial cooling water to reduce biofouling in heat transfer equipment's. The chlorination in drinking water produces germicidal effect and thus reduces the bacterial counts. At NAPS the water quality is good and mild doses of chlorine (5 ppm) two times a day, as envisaged in design is noticed to be satisfactory. The chlorination of recirculating condenser cooling water presently is being done with the established doses for a fixed time twice a day. Some of the problems noticed with the chlorination process are : Corrosion of constructional material of chlorination plant and equipment's and pipelines causing large input of efforts on maintenance for keeping high availability of the chlorination plant. In addition to this, the leakages in the equipment could be a potential safety hazard. The effectiveness of chlorine is observed to be less in alkaline pH (above 9.0) as encountered at NAPS. This results is large quantities of chlorine injection for extended periods. The cost of chlorine and bleaching powder keeps fluctuating in the market as noticed in past few years. Many a times this results in scarcity of chlorine/bleaching powder causing interruption in biofouling control programme. Hence it was felt prudent to work on the alternative biocides which could be cost effective, non-polluting and nature and user

  20. Effect of silica fume addition on the PGNAA measurement of chlorine in concrete

    Energy Technology Data Exchange (ETDEWEB)

    Naqvi, A.A. [Department of Physics, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia)], E-mail: aanaqvi@kfupm.edu.sa; Maslehuddin, M. [Center for Engineering Research, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Garwan, M.A. [Department of Physics, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Nagadi, M.M. [Center for Engineering Research, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Al-Amoudi, O.S.B. [Department of Civil Engineering, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Raashid, M.; Khateeb-ur-Rehman [Department of Physics, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia)

    2010-03-15

    Pozzolanic materials, such as fly ash (FA), silica fume (SF), and blast furnace slag (BFS) are added to Portland cement in concrete to prevent reinforcement steel corrosion in concrete. Further preventive measure against reinforcement steel corrosion require monitoring of chloride salts concentration in concrete using non-destructive techniques, such as the prompt gamma-ray neutron activation analysis (PGNAA) technique. Due to interferences between gamma-rays from chlorine and calcium in PGNAA technique, detection limit of chlorine in concrete strongly depends upon calcium concentration in concrete. SF mainly contains silica and its addition to cement concrete reduces overall concentration of calcium in concrete. This may result in an improvement in detection limit of chlorine in SF-based concrete in PGNAA studies. Particularly for chlorine detection using 6.11 and 6.62 MeV prompt gamma-rays that strongly interfere with 6.42 MeV prompt gamma-rays from calcium. In this study, SF was added to Portland cement to prevent concrete reinforcement steel from corrosion. The chlorine concentration in SF cement concrete specimens containing 0.2-3.0 wt% chlorine was measured through yield of 1.16, 1.95, 6.11, 6.62, 7.41, 7.79, and 8.58 MeV chlorine gamma-rays using PGNAA technique. An excellent agreement was noted between the experimental yield of the prompt gamma-rays and the gamma-ray yield calculated through the Monte Carlo simulations. Further the minimum detectable concentration (MDC) of chlorine in SF cement concrete was calculated and compared with the MDC values of chlorine in plain concrete and concrete mixed with fly ash cement. The MDC of chlorine in SF-based concrete through 6.11 MeV, and 6.62 MeV chlorine gamma-rays was found to be improved as compared to those in plain concrete and concrete mixed with fly ash cement.