Science.gov

Sample records for chlorinated hydrocarbon residues

  1. Chlorinated hydrocarbon and mercury residues in woodcock in the United States, 1970-71

    USGS Publications Warehouse

    Clark, D.R., Jr.; McLane, M.A.R.

    1974-01-01

    During Late 1970 and early 1971, 229 woodcock (Philohela minor) were collected from 23 Eastern and Midwestern States. Analyses for chlorinated hydrocarbons and mercury in these migratory birds showed generally low levels which are not considered dangerous to human consumers. In this survey, Louisiana woodcock had lower residues of heptachlor epoxide and DDE than those tested in a 1965 survey. PCB levels, however, may have increased. Mirex levels were greatest in Mississipi and Louisiana woodcock. Pooling of birds and averaging of individually analyzed birds did not provide equivalent estimates of equivalent residues; pool values tended to be larger and more variable. Levels of six chlorinated hydrocarbons and mercury were negatively correlated with the latitude of the collection site. However, this relationship seemed weakest for PCB's. Among eight chemical residues, PCB levels were most often correlated with levels of the other seven. Levels of chlorinated hydrocarbons in wings were correlated with levels in breast muscle and in carcass; however, mean levels of certain residues differed significantly among wing, muscle, and carcass even when compared on a lipid basis.

  2. Polychlorinated biphenyl and other chlorinated hydrocarbon residues in adipose tissue of Canadians

    SciTech Connect

    Mes, J.; Davies, D.J.; Turton, D.

    1982-01-01

    The data reported in this paper are part of a continuing monitoring program of chlorinated hydrocarbons in adipose tissue of Canadians in order to determine a possible trend in both the disappearance of restricted OC pesticides, such as p,p,-DDT, as well as the appearance of new environmental contaminants, such as hexachloro-1,3-butadiene (HCBD).

  3. Chlorinated hydrocarbon residues in Baikal seal (Phoca sibirica) from Lake Baikal: Levels, patterns, and metabolism

    SciTech Connect

    Nakata, H.; Tanabe, S.; Tatsukawa, R.; Amano, M.; Miyazaki, N.; Petrov, A.

    1995-12-31

    Contamination of chlorinated hydrocarbons such as DDTs (DDT and its metabolites), PCBs (polychlorinated biphenyls), CHLs (chlordane compounds) and HCHs (hexachlorocyclohexanes) was assessed in the blubber of Baikal seal (Phoca sibirica) and their fish diet collected from Lake Baikal in 1992. Higher concentrations of DDTs and PCBs were detected, ranging from 4.9 to 160 {micro}g/g and 3.5 to 64 {micro}g/g on a lipid weight basis, respectively, whereas levels of CHLs and HCHs were approximately one or three orders of magnitude lower than those of DDTs and PCBs. The average of DDTs concentrations in adult male Baikal seals were about an order of magnitude higher than those reported for seals in the North Sea around UK and comparable to grey seal in the Baltic Sea, indicating that Baikal seals are categorized in a highly contaminated group. A positive age dependent accumulation of DDTs, PCBs and CHLs was found in male, while a steady-state was observed in female which attributes to the reproductive transfer, mainly lactation, of these chemicals. On the basis of contaminant burdens in adult seals, it was estimated that adult females transfer about 19% and 14% of their DDT and PCB body burdens to their pups during a reproductive process. Based on the data from isomer specific analysis of PCBs, it can be suggested that Baikal seals have higher capacity to metabolize congeners with vicinal H-atoms in meta, para positions than those of marine mammals.

  4. The historical residue trend of chlorinated hydrocarbons in the Agassiz Ice Cap, Ellesmere I., Canada

    SciTech Connect

    Gregor, D.J.; Peters, A.J.; Backus, S.; Fisher, D.; Zheng, J.

    1995-12-31

    Current detailed measurements of contaminant deposition can not provide a historical perspective except through long term monitoring programs. In the Arctic, ice caps provide an alternative to lake sediments in that the annual snow layers reflect the atmospheric deposition. As a result of the remoteness of the Agassiz Ice Cap (80{degree}49`50``N, 72{degree}56`30``W) and the limited summer melt, annual layers undergo little chemical change, especially after the first summer season, and therefore provide a well defined historical record. PCBs were first measured above detection limit in the core in the late 1950`s. Mean concentration of {Sigma}PCB over the thirty year period is 3.5 ({+-}1.3) ng. L{sup {minus}1}. {Sigma}PCB is dominated by the lower chlorinated congeners with only infrequent detections of congeners with eight or more chlorines. Deposition peaked at 930 ng.m{sup {minus}2}.a{sup {minus}1} in 1967/68 and decreased to 90 ng.m{sup {minus}2}.a{sup {minus}1} in 1980/81. Since 1980/81, deposition has again increased to a local maximum of 850 ng.m{sup {minus}2}.a{sup {minus}1} in 1989/90. PAHs are detectable throughout the sampling period. Only 7 individual PAHs were above the quantification limits including naphthalene (accounting for an overall mean of 88% of the {Sigma}PAH) acenaphthene, fluorene, phenanthrene, fluoranthene, pyrene and chrysene. No PAHs with five or more aromatic rings were observed to be present above the detection limits. The flux of PAHs to the Ice Cap remained relatively constant from 1790 to 1940 at approximately 3 {micro}g.m{sup {minus}2}.a{sup {minus}1}. The period 1940 to 1980 is dominated by a large increase in deposition peaking at 70 {micro}g.m{sup {minus}2}.a{sup {minus}1} in the early 1970`s. The final period, 1980 to 1993 shows a steady increase by a factor of about 2 from a minimum of 10--20 {micro}g.m{sup {minus}2}.a{sup {minus}1}.

  5. Process for Photochemical Chlorination of Hydrocarbons

    DOEpatents

    Beanblossom, W S

    1951-08-28

    A process for chlorination of a major portion of the hydrogen atoms of paraffinic hydrocarbons of five or more carbon atoms may be replaced by subjecting the hydrocarbon to the action of chlorine under active light. The initial chlorination is begun at 25 to 30 deg C with the chlorine diluted with HCl. The later stages may be carried out with undiluted chlorine and the temperature gradually raised to about 129 deg C.

  6. Chlorinated hydrocarbons in peat

    SciTech Connect

    Rapaport, R.A.

    1985-01-01

    Concentrations (ng/g), accumulation rates (ug/m/sup 2/=yr) and burdens were determined for DDT (1,1,1-trichlorophenyl2-2'bis(p-chlorophenyl)ethane), polychlorinated biphenyls. Toxaphene, hexachlorobenzene (HCB) and a,b,g-hexachlorocyclohexanes (HCHs) in peat cores taken across the mid-latitudes of North America. Because peat bogs are ombrotrophic, thereby receiving all contaminant inputs from the atmosphere and because peat cores were dated, atmospheric input functions were constructed for all of the compounds listed above excepting the HCHs. Compound inventories (burdens) in peat cores of PCBs, HCB, HCHs, Toxaphene, DDT, Pb and Zn were compared, indicating a strong influence from areas proximate to industrial sources and the atmospheric transport from source regions. Untransformed parent DDT (p,p' and o,p'-DDT) in surface peat and in precipitation provides evidence for the long range transport of DDT from neighboring countries where use has increased over the past 10-15 years. Present accumulation rates of DDT in peat are about 10-20% of maximum levels associated with peak use in the US around 1960. The DDT input function that was developed can be used to date peat cores. Transformations of DDT and PCBs were also examined in peat cores. First order transformation rates of DDT (p,p' and o,p') to DDD in anaerobic peat core environments ranged from 0.03 to 0.09 yr/sup -1/ with differences related to temperature. Aerobic transformation of PCB congeners in peat cores and microcosms was rapid for 2,3 and several 4 chlorinated congeners (T/sub 1/2 less than or equal to 0.2 to 3 years) and declined with increasing chlorine number.

  7. BOOSTER CHLORINATION FOR MANAGING DISINFECTANT RESIDUALS

    EPA Science Inventory

    Booster chlorination is an approach to residual maintenance in which chlorine is applied at strategic locations within the distribution system. Situations in which booster chlorination may be most effective for maintaining a residual are explained informally in the context of a ...

  8. RELATIONSHIPS BETWEEN LABORATORY AND PILOT-SCALE COMBUSTION OF SOME CHLORINATED HYDROCARBONS

    EPA Science Inventory

    Factors governing the occurence of trace amounts of residual organic substance emmissions (ROSEs) in full-scale incierators are not fully understood. Pilot-scale spray combustion expereiments involving some liquid chlorinated hydrocarbons (CHCs) and their dilute mixtures with hy...

  9. Flame stabilization in chlorine-hydrocarbon mixtures

    SciTech Connect

    Steblev, A.V.

    1986-11-01

    The authors determine the limits of stable steady-state combustion of binary mixtures of methane, propane, ethylene, and chlorine using cylindrical stabilizers of various diameters. The studies were performed on Bunsen burners. Two series of experiments were performed. The first studied the effect of stabilizer size on the limits of flame stabilization in mixtures of fixed composition having the highest flame velocity; the second studied the effect on combustion limits of mixture composition for the fixed stabilizer diameter at which the combustion limits were widest. The principles established by these experiments are used as contributing factors in the design of high-output combustion chambers for hydrocarbon-chlorine mixtures.

  10. Behavioral toxicology, risk assessment, and chlorinated hydrocarbons

    SciTech Connect

    Evangelista de Duffard, A.M.; Duffard, R.

    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.

  11. Behavioral toxicology, risk assessment, and chlorinated hydrocarbons.

    PubMed Central

    Evangelista de Duffard, A M; Duffard, R

    1996-01-01

    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 changes 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. PMID:9182042

  12. Chlorinated hydrocarbon contaminants in arctic marine mammals.

    PubMed

    Norstrom, R J; Muir, D C

    1994-09-16

    By 1976, the presence of chlorinated hydrocarbon contaminants (CHCs) had been demonstrated in fur seal (Callorhinus ursinus), ringed seal (Phoca hispida), hooded seal (Cystophora cristata), bearded seal (Erignathus barbatus), walrus (Obdobenus rosmarus divergens), beluga (Delphinapterus leucas), porpoise (Phocoena phocoena) and polar bear (Ursus maritimus) in various parts of the Arctic. In spite of this early interest, very little subsequent research on contaminants in Arctic marine mammals was undertaken until the mid-1980s. Since that time, there has been an explosion of interest, resulting in a much expanded data base on contaminants in Arctic marine mammals. Except in the Russian Arctic, data have now been obtained on the temporospatial distribution of PCBs and other contaminants in ringed seal, beluga and polar bear. Contaminants in narwhal (Monodon monoceros) have also now been measured. On a fat weight basis, the sum of DDT-related compounds (S-DDT) and PCB levels are lowest in walrus (< 0.1 microgram/g), followed by ringed seal, (0.1-1 microgram/g range). Levels are an order of magnitude higher in beluga and narwhal (1-10 micrograms/g range). It appears that metabolism and excretion of S-DDT and PCBs may be less efficient in cetaceans, leading to greater biomagnification. Polar bears have similar levels of PCBs as cetaceans (1-10 micrograms/g), but with a much simpler congener pattern. DDE levels are lowest in polar bear, indicating rapid metabolism. Effects of age and sex on residue levels are found for all species where this was measured. Among cetaceans and ringed seal, sexually mature females have lower levels than males due to lactation. Although PCB levels in adult male polar bears are about twice as high as females, there is only a trivial age effect in either sex apart from an initial decrease from birth to sexual maturity (age 0-5). Comparison of levels of S-DDT and PCBs in Arctic beluga and ringed seal with those in beluga in the Gulf of St

  13. Stable isotope investigations of chlorinated aliphatic hydrocarbons.

    SciTech Connect

    Abrajano, T.; Heraty, L. J.; Holt, B. D.; Huang, L.; Sturchio, N. C.

    1999-06-01

    Stable isotope ratio measurements for carbon (C) and chlorine (Cl) can be used to elucidate the processes affecting transformation and transportation of chlorinated aliphatic hydrocarbons (CAHs) in the environment. Methods recently developed in our laboratory for isotopic analysis of CAHs have been applied to laboratory measurements of the kinetic isotope effects associated with aerobic degradation of dichloromethane (DCM) and with both anaerobic and aerobic cometabolic degradation of trichlomethene (TCE) in batch and column microbial cultures. These experimental determinations of fractionation factors are crucial for understanding the behavior of CAHs in complex natural systems, where the extent of biotransformation can be masked by dispersion and volatilization. We have also performed laboratory investigations of kinetic isotope effects accompanying evaporation of CAHs, as well as field investigations of natural attenuation and in situ remediation of CAHs in a number of contaminated shallow aquifers at sites operated by the federal government and the private sector.

  14. Hydrocarbon and chlorinated hydrocarbon-soluble magnesium dialkoxides

    SciTech Connect

    Kamienski, C.W.

    1988-05-31

    This patent describes a process for the preparation of hydrocarbon or chlorinated hydrocarbon solvent solutions of magnesium dialkoxides, which comprises reacting a suspension of magnesium metal or magnesium amide, or a solution of a dialkyimagnesium compound, in a volatile hydrocarbon or chlorinated hydrocarbon solvent with an alcohol selected from the group of (a) aliphatic, cycloaliphatic and acyclic C/sub 5/-C/sub 18/ beta- and gamma-alkyl-substituted secondary and tertiary monohydric alcohols; or (b) mixtures of the (a) alcohols with C/sub 3/-C/sub 18/ aliphatic or cycloaliphatic beta- and gamma-alkyl-unsubstituted secondary or tertiary alcohols; or (c) mixtures of the (a) alcohols with C/sub 1/-C/sub 18/ aliphatic primary unsubstituted and 2-alkyl-substituted alcohols; the mole ratios of the (a) to the (b), and the (a) to the (c), alcohols being 1 of the (a) alcohols to 0.1 to 2 of the (b) and/or the (c) alcohols.

  15. Biological monitoring of chlorinated hydrocarbon solvents

    SciTech Connect

    Monster, A.C.

    1986-08-01

    The possibility of biological monitoring of exposure to some volatile, halogenated hydrocarbons will be discussed. Most of these agents are widely used as solvents. All agents act on the nervous system as narcotics and differ widely in toxicity. Most of the solvents undergo biotransformation to metabolites. This allows biological assessment of exposure by measurement of the solvent and/or metabolites in exhaled air, blood, and/or urine. However, the same metabolites may occur with exposure to different chlorinated hydrocarbons, eg, trichloroethanol and trichloroacetic acid from exposure to trichloroethene, tetrachloroethene, and 1,1,1-trichloroethane. On the other hand, these agents differ widely in the percentage that is metabolized. There are large gaps in our knowledge, however, and much research will have to be carried out before even tentative data can be established for most of the solvents.

  16. Chlorinated hydrocarbons in women with repeated miscarriages.

    PubMed Central

    Gerhard, I; Daniel, V; Link, S; Monga, B; Runnebaum, B

    1998-01-01

    This study was conducted to investigate a possible etiological role of chlorinated hydrocarbons in the pathogenesis of repeated miscarriages. The blood levels of chlorinated hydrocarbons [CHCs: pentachlorophenol, hexachlorocyclohexane, hexachlorobenzene, the dichlorodiphenyltrichloroethane (DDT) group, polychlorinated biphenyls] were determined in 89 women with repeated miscarriages, who were referred to the University Hospital of Obstetrics and Gynecology of Heidelberg for investigations between 1989 and 1993, and compared to a previously investigated reference population. In more than 20% of the women, at least one of the CHC levels exceeded the reference range. CHC levels did not differ significantly between women with primary or secondary and early or late miscarriages; neither did they differ between women with hormonal or immunological disorders as causes of repeated miscarriages or women with idiopathic repeated miscarriages. No significant associations were detected between CHC levels and further conceptions or the outcome of further pregnancies. As significant associations were found between increasing CHC blood concentrations and immunological and hormonal changes, CHCs may have an impact on the pregnancy course in certain cases. PMID:9755145

  17. Chlorinated hydrocarbons in lichen and moss samples from the Antarctic Peninsula

    SciTech Connect

    Bacci, E.; Calamari, D.; Gaggi, C.; Fanelli, R.; Focardi, S.; Morosini, M.

    1986-01-01

    The concentrations of some chlorinated hydrocarbon residues (HCB, HCH isomers, p,p'DDT and DDE, PCB cogeners) in lichen and moss samples from the Antarctic Peninsula are reported and compared with available data from other parts of the world. The use of these materials as indicators of tropospheric contamination levels in Antarctica is discussed.

  18. Chlorinated hydrocarbons and eggshell changes in raptorial and fish-eating birds

    USGS Publications Warehouse

    Hickey, J.J.; Anderson, D.W.

    1968-01-01

    Catastrophic declines of three raptorial species in the United States have been accompanied by decreases in eggshell thickness that began in 1947, have amounted to 19 percent or more, and were identical to phenomena reported in Britain. In 1967, shell thickness in herring gull eggs from five states decreased with increases in chlorinated hydrocarbon residues.

  19. In-situ demonstration of radio-frequency enhanced chlorinated hydrocarbon remediation

    SciTech Connect

    Kasevich, R.S.; Price, S.L.; Faust, D.L.; Jarosch, T.R.

    1994-06-01

    This paper discusses the results of a successful demonstration of radio frequency (RF) heating for enhanced chlorinated hydrocarbon remediation at the M-Area Seepage Basin of the Department of Energy`s Savannah River Site. RF heating was integrated with soil vapor extraction (SVE) to enhance the release of residual volatile chlorinated hydrocarbons which are concentrated in low permeable clay lenses in the unsaturated zone. Participants in this effort consisted of the Westinghouse Savannah River Technology Center; the Westinghouse Science and Technology Center (Pittsburgh, PA); and KAI Technologies, Inc. which provided the RF technology. Additionally, a better understanding of RF heating technology is gained through a description of the RF heating system.

  20. Persistence of chlorinated hydrocarbon contamination in a California marine ecosystem

    SciTech Connect

    Young, D.R.; Gossett, R.W.; Heesen, T.C.

    1989-01-01

    Despite major reductions in the dominant DDT and polychlorinated biphenyls (PCB) input off Los Angeles (California, U.S.A.) in the early 1970s, the levels of these pollutants decreased only slightly from 1972 to 1975 both in surficial bottom sediments and in a flatfish bioindicator (Dover sole, Microstomus pacificus) collected near the submarine outfall. Concentrations of these pollutants in the soft tissues of the mussel Mytilus californianus, collected intertidally well inshore of the highly contaminated bottom sediments, followed much more closely the decreases in the outfall discharges. These observations suggest that contaminated sediments on the seafloor were the principal (although not necessarily direct) cause of the relatively high and persistent concentrations of DDT and PCB residues in tissues. The study indicated that residues of the higher-molecular-weight chlorinated hydrocarbons, such as DDT and PCB, can be highly persistent once released to coastal marine ecosystems and that their accumulation in surficial bottom sediments is the most likely cause of this persistence observed in the biota of the discharge zone.

  1. Shock-tube pyrolysis of chlorinated hydrocarbons - Formation of soot

    NASA Technical Reports Server (NTRS)

    Frenklach, M.; Hsu, J. P.; Miller, D. L.; Matula, R. A.

    1986-01-01

    Soot formation in pyrolysis of chlorinated methanes, their mixtures with methane, and chlorinated ethylenes were studied behind reflected shock waves by monitoring the attenuation of an He-Ne laser beam. An additional single-pulse shock-tube study was conducted for the pyrolysis of methane, methyl chloride, and dichloromethane. The experiments were performed at temperatures 1300-3000 K, pressures of 0.4-3.6 bar, and total carbon atom concentrations of 1-5 x 10 to the 17th atoms cu cm. The amounts of soot produced in the pyrolysis of chlorinated hydrocarbons are larger than that of their nonchlorinated counterparts. The sooting behavior and product distribution can be generally explained in terms of chlorine-catalyzed chemical reaction mechanisms. The pathway to soot from chlorinated methanes and ethylenes with high H:Cl ratio proceeds via the formation of C2H, C2H2, and C2H3 species. For chlorinated hydrocarbons with low H:Cl ratio, the formation of C2 and its contribution to soot formation at high temperatures becomes significant. There is evidence for the importance of CHCl radical and its reactions in the pyrolysis of dichloromethane.

  2. Transformation of Chlorinated Hydrocarbons on Synthetic Green Rusts

    EPA Science Inventory

    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...

  3. TURBULENT FLAME REACTOR STUDIES OF CHLORINATED HYDROCARBON DESTRUCTION EFFICIENCY

    EPA Science Inventory

    Four mixtures of C1 and C2 chlorinated hydrocarbons, diluted in heptane, were burned in a Turbulent Flame Reactor (TFR) under high and low oxygen conditions. Emissions of undestroyed feed, stable organic by-products, carbon monoxide, carbon dioxide and oxyg...

  4. Microemulsion formation with mixed chlorinated hydrocarbon liquids

    SciTech Connect

    Baran, J.R. Jr.; Pope, G.A.; Wade, W.H.; Weerasooriya, V.; Yapa, A. )

    1994-11-01

    Mixing rules for water/chlorocarbon/anionic surfactant systems have been studied. It was found that the behavior of chlorocarbons parallels the ideal mixing rules for hydrocarbons. The polarity of some chlorocarbons prevented a direct determination of electrolyte concentration and solubilization parameter for optimum formulations. These values were obtained by extrapolation and have been tabulated. Various complex mixtures containing chlorocarbons and hydrocarbons were prepared and their experimental optimum salinities were compared to calculated values.

  5. Estimating The Thermodynamics And Kinetics Of Chlorinated Hydrocarbon Degradation

    SciTech Connect

    Bylaska, Eric J.

    2006-08-01

    Many different degradation reactions of chlorinated hydrocarbons are possible in natural ground waters. In order to identify which degradation reactions are important, a large number of possible reaction pathways must be sorted out. Recent advances in ab initio electronic structure methods have the potential to help identify relevant environmental degradation reactions by characterizing the thermodynamic properties of all relevant contaminant species and intermediates for which experimental data is usually not available, as well as provide activation energies for relevant pathways. In this paper, strategies based on ab initio electronic structure methods for estimating thermochemical and kinetic properties of reactions with chlorinated hydrocarbons are presented. Particular emphasis is placed on strategies that are computationally fast and can be used for large organochlorine compounds such as 4,4?-DDT.

  6. Aerobic microorganism for the degradation of chlorinated aliphatic hydrocarbons

    DOEpatents

    Fliermans, Carl B.

    1989-01-01

    A chlorinated aliphatic hydrocarbon-degrading microorganism, having American Type Culture Collection accession numbers ATCC 53570 and 53571, in a biologically pure culture aseptically collected from a deep subsurface habitat and enhanced, mineralizes trichloroethylene and tetrachloroethylene to HCl, H.sub.2 O and Co.sub.2 under aerobic conditions stimulated by methane, acetate, methanol, tryptone-yeast extract, propane and propane-methane.

  7. Chlorinated hydrocarbons in flatfishes from the Southern California, USA, Bight

    SciTech Connect

    Schiff, K.; Allen, M.J.

    2000-06-01

    Although inputs of chlorinated hydrocarbon compounds to the Southern California Bight (SCB) are presently low, historical deposits represent a source of bioaccumulation potential to sediment-associated fauna. To assess this bioaccumulation potential, 14 chlorinated hydrocarbon classes were measured in livers of three species of flatfish collected from 63 randomly selected sites on the coastal shelf between Point Conception and the United States-Mexico international border. Tissue contamination was widespread throughout the SCB, but was limited to just two chlorinated hydrocarbon classes. Virtually 100% of Pacific sanddab (Citharichthys sordidus) and longfin sanddab (Citharichthys xanthostigma) populations were estimated to be contaminated with dichlorodiphenyltrichloroethane (total DDT = sum of o.p{prime} and p,p{prime} isomers of DDT + dichlorodiphenyldichloroethylene [DDE] + dichlorodiphenyldichloroethane [DDD]) and/or polychlorinated biphenyls (total PCBs). Total DDT also contaminated the majority (64%) of the Dover sole (Microstomus pacificus) population in the SCB. Total PCB measurements in tissues of SCB flatfish were dominated by 12 congeners (52, 66, 87, 101, 105, 118, 128, 138, 153, 170, 180, and 187), which averaged 95% of the combined mass of the 27 congeners analyzed. Sediment concentrations accounted for most of the variability observed in tissue concentrations for 8 of these 12 congeners and total PCBs. Normalized sediment concentrations were also significantly correlated to normalized tissue concentrations for total DDT and p,p{prime}-DDE. Tissue concentrations measured in this study from reference areas of the SCB were compared to tissue concentrations measured form reference areas in studies conducted in 1977 and 1985. Total DDT and total PCB liver concentrations were found to have decreased one to two orders of magnitude in pacific and longfin sanddabs between 1985 and 1994. Total DDT and total PCB liver concentrations decreased 5- to 35-fold in

  8. Supported metal nanoparticles for the remediation of chlorinated hydrocarbons

    NASA Astrophysics Data System (ADS)

    Schrick, Bettina

    Zero valent iron filings are currently being used in pilot scale field studies to dehalogenate toxic chlorinated hydrocarbons from contaminated surface- and groundwater. Iron filings reduce trichloroethylene (TCE), a model contaminant, via two interconnected degradation pathways: (a) reductive beta-elimination and (b) sequential hydrogenolysis, in which each chlorine atom is sequentially replaced by hydrogen. For the latter pathway, problems arise because the dehalogenation rate decreases as the number of chlorine atoms in the molecule decreases. Therefore, some of the products formed, such as vinyl chloride (VC), are more toxic than the parent compound (TCE), and are only slowly reduced by iron. To improve the rate, cost and technique of remediation for chlorinated hydrocarbons, zero valent nickel-iron (Ni-Fe) nanoparticles have been developed. To elucidate the dehalogenation reaction and particularly the product distributions from a mechanistic standpoint, the roles that nickel and iron play in the dehalogenation of TCE were studied. On the bimetallic particles, the reaction occurs by nickel-catalyzed hydrodechlorination. As the iron actively corrodes, the cathodically protected nickel surface chemisorbs hydrogen ions, and TCE adsorbed to the Ni surface is thus hydrogenated. This reaction competes kinetically with the evolution of molecular hydrogen. Hydrogenolysis of the C-Cl bond results in the formation of linear, as well as branched saturated and unsaturated hydrocarbons. Dispersing the nanometals onto high surface area supports, such as hydrophilic carbon or polyacrylic acid (PAA), provides a delivery vehicle for the reactive nanoparticles. The support acts as a nanometal carrier, and may also help preconcentrate the toxins, and provide a conductive pathway for electron transfer. In general, supports are expected to stabilize the nanoparticles and give an increased surface to volume ratio. The carbon- and PAA-supported nanometals form a permanent suspension

  9. Carbon and chlorine isotopologue fractionation of chlorinated hydrocarbons during diffusion in water and low permeability sediments

    NASA Astrophysics Data System (ADS)

    Wanner, Philipp; Hunkeler, Daniel

    2015-05-01

    To identify reactive processes in diffusion dominated water-saturated systems using compound-specific isotope analysis (CSIA), the effect of the diffusive transport process on isotope ratios needs to be known. This study aims to quantify the magnitude of carbon and chlorine isotopologue fractionation of two chlorinated hydrocarbons (trichloroethene (TCE) and 1,2-dichloroethane (1,2-DCA)) during diffusion in the aqueous phase and to relate for the first time laboratory with field results. Diffusion coefficient ratios in the aqueous phase were experimentally quantified with a modified Stokes diffusion cell. The experiment revealed a significant shift of carbon and chlorine isotopologue ratios of TCE and 1,2-DCA during diffusion. For both TCE and 1,2-DCA, the magnitude of the shift of chlorine isotopologue ratios was larger (TCE: D132/D130 = 0.99963 ± 0.00003; 1,2-DCA: D102/D100 = 0.99939 ± 0.00003) in comparison to carbon isotopologue ratios (TCE: D131/D130 = 0.99978 ± 0.00006; 1,2-DCA: D101/D100 = 0.99977 ± 0.00004), which is consistent with the larger mass difference between stable chlorine compared to carbon isotopes. Determined diffusion coefficients for carbon and chlorine isotopologues of TCE and 1,2-DCA follow an inverse power law form (D ∝m-β) with β < 0.5 revealing that the magnitude of isotopologue fractionation of TCE and 1,2-DCA is lower than in the previously postulated kinetic theory (D ∝m-0.5). To relate laboratory with field results, a water-saturated clay core from a VOC contaminated site was retrieved and subsampled as a function of depth to assess possible shifts in isotopologue ratios during downward diffusion of VOCs into the low permeable clay. Observed small shifts of TCE carbon and chlorine isotopologue ratio profiles were consistent with laboratory determined diffusion coefficient ratios, demonstrated by a 1D-diffusion model. Further 1D-simulations for shorter diffusion periods (5-10 years) than observed in the retrieved clay core

  10. Iron-carbon composites for the remediation of chlorinated hydrocarbons

    NASA Astrophysics Data System (ADS)

    Sunkara, Bhanu Kiran

    This research is focused on engineering submicron spherical carbon particles as effective carriers/supports for nanoscale zerovalent iron (NZVI) particles to address the in situ remediation of soil and groundwater chlorinated contaminants. Chlorinated hydrocarbons such as trichloroethylene (TCE) and tetrachloroethylene (PCE) form a class of dense non-aqueous phase liquid (DNAPL) toxic contaminants in soil and groundwater. The in situ injection of NZVI particles to reduce DNAPLs is a potentially simple, cost-effective, and environmentally benign technology that has become a preferred method in the remediation of these compounds. However, unsupported NZVI particles exhibit ferromagnetism leading to particle aggregation and loss in mobility through the subsurface. This work demonstrates two approaches to prepare carbon supported NZVI (iron-carbon composites) particles. The objective is to establish these iron-carbon composites as extremely useful materials for the environmental remediation of chlorinated hydrocarbons and suitable materials for the in situ injection technology. This research also demonstrates that it is possible to vary the placement of iron nanoparticles either on the external surface or within the interior of carbon microspheres using a one-step aerosol-based process. The simple process of modifying iron placement has significant potential applications in heterogeneous catalysis as both the iron and carbon are widely used catalysts and catalyst supports. Furthermore, the aerosol-based process is applied to prepare new class of supported catalytic materials such as carbon-supported palladium nanoparticles for ex situ remediation of contaminated water. The iron-carbon composites developed in this research have multiple functionalities (a) they are reactive and function effectively in reductive dehalogenation (b) they are highly adsorptive thereby bringing the chlorinated compound to the proximity of the reactive sites and also serving as adsorption

  11. Determination of Residual Chlorine and Turbidity in Drinking Water. Instructor's Manual.

    ERIC Educational Resources Information Center

    Office of Water Program Operations (EPA), Cincinnati, OH. National Training and Operational Technology Center.

    This instructor's guide presents analytical methods for residual chlorine and turbidity. Topics include sample handling, permissable concentration levels, substitution of residual chlorine for bacteriological work, public notification, and the required analytical techniques to determine residual chlorine and turbidity. This publication is intended…

  12. Determination of Residual Chlorine and Turbidity in Drinking Water. Student Manual.

    ERIC Educational Resources Information Center

    Office of Water Program Operations (EPA), Cincinnati, OH. National Training and Operational Technology Center.

    This student's manual covers analytical methods for residual chlorine and turbidity. Topics include sample handling, permissable concentration levels, substitution of residual chlorine for bacteriological work, public notification, and the required analytical techniques to determine residual chlorine and turbidity. The publication is intended for…

  13. Chlorinated hydrocarbons in the Sargasso sea atmosphere and surface water.

    PubMed

    Bidleman, T F; Olney, C E

    1974-02-01

    Polychlorinated biphenyls (PCB), DDT, and chlordane concentrations were measured in air sampled from a tower on the south shore of Bermuda and in Sargasso Sea surface water approximately 80 to 320 kilometers south of Bermuda. The atmospheric chlorinated hydrocarbons appeared to be gaseous, and the DDT concentration was two orders of magnitude higher than previously reported particulate values. The PCB and DDT were enriched in the surface microlayer (150 micrometers) relative to their concentrations in water at a depth of 30 centimeters. Atmospheric residence times for PCB and DDT of 40 to 50 days, calculated from the concentrations in the air and water, are 20 times shorter than values previously estimated for DDT from rainfall and DDT production data.

  14. Effects of chlorinated hydrocarbon insecticides upon quail and pheasants

    USGS Publications Warehouse

    DeWitt, J.B.

    1955-01-01

    Previous studies had shown that heavy or repeated applications of DDT resulted in decreases.in bird populations, but long-range effects of this and other chlorinated hydrocarbon insecticides had not been fully evaluated. Experiments were conducted to determine toxiCitY to quail and pheasants of aldrin, dieldrin, endrin, and strobane, and to determine effects of these compounds upon survival, growth, and reproduction....Feeding of diets containing 0.02% DDT to breeding quail resulted in significant decreases in hatchability of eggs and in viability of chiCks. Similar results were obtained by feeding 0.001% dieldrin, but effects upon reproduct.ion of short-term feeding of aldrin and endrin could not be determined....Aldrin, dieldrin, and endrin were lethal to both male and female quail when fed at levels of 0.0005% in the diets. Female pheasants appeared more resistant than males to the effects of these compounds.

  15. Bioconcentration of chlorinated hydrocarbons from sediment by oligochaetes

    SciTech Connect

    Connell, D.W.; Bowman, M.; Hawker, D.W.

    1988-12-01

    Previously published data on the accumulation of 15 chlorinated hydrocarbons from sediment by oligochaetes have been interpreted on the basis of bioconcentration from interstitial water. Calculation of the interstitial water concentration allowed determination of uptake and clearance rate constants together with bioconcentration factors (KB) for these compounds. These three factors each exhibited a systematic relationship to the octanol/water partition coefficient (KOW). The log KB versus log KOW relationship was roughly linear over the log KOW range from 4.4 to 6.4 and displayed an increasing nonlinear deviation for log KOW values greater than 6.4. These relationships are qualitatively similar to those established for other aquatic organisms where bioconcentration from water was the mechanism involved. This suggests that interstitial water may be the phase from which lipophilic compounds in sediment are bioconcentrated by oligochaetes. An expression relating the bioconcentration factor to the biotic concentration and various sediment characteristics has also been developed.

  16. A New, Rapid, Precise and Sensitive Method for Chlorine Stable Isotope Analysis of Chlorinated Aliphatic Hydrocarbons

    NASA Astrophysics Data System (ADS)

    van Acker, M. R.; Shahar, A.; Young, E. D.; Coleman, M. L.

    2005-12-01

    Chlorinated aliphatic hydrocarbons (CAH) are recognized common groundwater contaminants. Because of their physico-chemical properties, their lifespan in groundwater is in the order of decades (Pankow and Cherry, 1996). Stable isotopes can play a role in determining the rate and extent of CAH attenuation (Slater, 2003). The use of chlorine has been hampered by the current time consuming and insensitive analytical methods. We present a new analytical procedure to measure chlorine stable isotope values using a gas chromatograph coupled to a multi-collector inductively coupled mass spectrometer (GC-MC-ICP-MS). The GC has a Porapack Q packed column. The carrier gas was helium and the temperature was constant at 160°C. The GC was coupled to the MC-ICP-MS by heated stainless steel tubing. Our high resolution spectra showed that 37Cl is free of its main interference 36Ar-H over a range of 0.004 amu. Two pure CAH, trichloroethene (TCE) and tetrachloroethene (PCE), were used for zero enrichment (sample relative to itself) and standard-sample difference measurements. Integrations and background corrections of transient signals were performed using Microsoft Excel after import of the raw data from the MC-ICPMS acquisition software. Zero enrichment tests with TCE and PCE yielded δ37Cl of -0.04±0.16‰ and -0.03±0.17‰, respectively, results for sample injections of 0.12 to 0.02 microliters. Accuracy was tested by injecting 0.24 microliters of a 50/50 mixture of TCE and PCE of known isotopic compositions as the difference between the two solvents was of paramount interest. The δ37Cl(TCE) value of PCE was -1.99±0.16‰. A highly satisfactory comparison with the conventional method is shown by published values for TCE and PCE, -2.04±0.12‰ and -0.30±0.14‰, respectively (Jendrzejewski et al., 2001), giving a δ37Cl(TCE) value for PCE of -2.34±0.18‰. These tests of the GC-MC-ICP-MS method showed that we can obtain reproducible and accurate Cl isotope values using an

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

    NASA Astrophysics Data System (ADS)

    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.

  18. Comparative ecotoxicology of halogenated hydrocarbon residues.

    PubMed

    Winteringham, F P

    1977-12-01

    The term ecotoxicology is adopted in the sense of a comparative and integrated study of the undesirable effects of trace contaminants on the range of fauna and flora of an "ecosystem" or of a defined part or unit thereof. The importance of population changes over long periods of time is stressed. Sources, usage, and global trends of representative halogenated hydrocarbon (HHC) residues which appear as trace contaminants of environment, food, and living organisms are briefly compared: industrial solvents and intermediates, chlorofluoromethanes as an atmospheric pollutant, methyl bromide as a food and soil residue, HCH (hexachlorobenzene) as a fungicide residue, DDT, lindane (gamma-hexachlorocyclohexane), and dieldrin as insecticide residues, and polychlorinated biphenyls (PCBs) as industrial contaminants. A simple mathematical approach to the problem of relating inputs, persistence, and steady-state residue levels is explained. Persistence and biodegradation of representative compounds are compared. Attention is drawn to the persistence of hexachlorobenzene, the p,p'-dichlorodiphenyl- and hexachlorocyclopentadiene-derived moities of HHC residues. Ecotoxicological effects and their implications are discussed comparatively under the indirect effects of atmospheric pollutants and direct and indirect effects of trace contaminants of soil and aquatic ecosystems. Some conclusions related to research and "impact monitoring" are drawn.

  19. Trends in chlorinated hydrocarbon levels in Hudson River basin sediments.

    PubMed Central

    Bopp, R F; Chillrud, S N; Shuster, E L; Simpson, H J; Estabrooks, F D

    1998-01-01

    Analysis of sections from dated sediment cores were used to establish geographic distributions and temporal trends of chlorinated hydrocarbon contaminant levels in sediments from natural waters of the Hudson River basin. Radiometric dating was based primarily on the depth distribution of 137(Cs) in the cores and on the occurrence of detectable levels of 7(Be) in surface sediment samples. Eighteen sampling sites included several along the main stem of the Hudson, its major tributaries, and components of the New York/New Jersey (NY/NJ) harbor complex. Drinking-water reservoirs were sampled to place upper limits on atmospheric inputs. Core sections were analyzed for polychlorinated biphenyls (PCBs), 1,1,1-trichloro-2,2-bis(p-chlorophenyl) ethane (DDT)-derived compounds, chlordane, and dioxins. Sediment concentrations of most contaminants at most sites have decreased significantly since the mid-1960s. The data provide a basinwide perspective on major point-source inputs of PCBs to the upper Hudson River and of 2,3,7,8-tetrachlorodibenzo-p-dioxin and DDT to the lower Passaic River. Evidence was found for significant but poorly characterized sources of PCBs and chlordane to the western NY/NJ harbor, and of highly chlorinated dioxins to the upstream sites on the main stem of the Hudson. The results indicate that analysis of dated sediment samples is a most effective and efficient monitoring tool for the study of large-scale geographic and temporal trends in levels of particle-associated contaminants. Images Figure 1 Figure 3 Figure 4 Figure 5 Figure 6 Figure 7 PMID:9703496

  20. Chlorinated hydrocarbons in plant foliage: an indication of the tropospheric contamination level

    SciTech Connect

    Gaggi, C.; Bacci, E.; Calamari, D.; Fanelli, R.

    1985-01-01

    Levels of some chlorinated hydrocarbons in foliage from the Italian peninsula and other countries of the world are reported. The use of plant leaves in monitoring and for a prediction of potential environmental distribution of persistent hydrophobic pollutants is discussed.

  1. Hydrous pyrolysis/oxidation process for in situ destruction of chlorinated hydrocarbon and fuel hydrocarbon contaminants in water and soil

    DOEpatents

    Knauss, Kevin G.; Copenhaver, Sally C.; Aines, Roger D.

    2000-01-01

    In situ hydrous pyrolysis/oxidation process is useful for in situ degradation of hydrocarbon water and soil contaminants. Fuel hydrocarbons, chlorinated hydrocarbons, polycyclic aromatic hydrocarbons, petroleum distillates and other organic contaminants present in the soil and water are degraded by the process involving hydrous pyrolysis/oxidation into non-toxic products of the degradation. The process uses heat which is distributed through soils and water, optionally combined with oxygen and/or hydrocarbon degradation catalysts, and is particularly useful for remediation of solvent, fuel or other industrially contaminated sites.

  2. Accumulation and diagenesis of chlorinated hydrocarbons in lacustrine sediments

    USGS Publications Warehouse

    Elsenreich, S.J.; Capel, P.D.; Robbins, J.A.; Bourbonniere, R.

    1989-01-01

    Two sediment cores were taken from the Rochester Basin of eastern Lake Ontario and analyzed for the radionuclides 210Pb and 137Cs and several high molecular weight chlorinated hydrocarbons (CHs). The two sites are geographically proximate but differ in sedimentation rate, permitting sedimentation-dependent processes to be factored out. The 210Pb chronology showed a mixed depth of 3-5 cm and an intrinsic time resolution of 11-14 years. Vertically integrated numbers of deposit-feeding oligochaete worms and burrowing organisms are insufficient to homogenize the sediment on the time scale of CH inputs, which are non steady state. U.S. production and sales of polychlorinated biphenyls (PCBs), DDT, Mirex, and hexachlorobenzene (HCB), as determinants of the shape of the input function, adequately predict the overall shape and, in many cases, details in the sedimentary profile. Sediment focusing factors (FF) inferred from 137Cs and 210Pb inventories averaged 1.17 and 1.74 for cores E-30 and G-32, respectively. This permitted CH accumulation rates to be corrected for focusing. Apparent molecular diffusion coefficients modeled for many of the CHs were about (1-3) ?? 10-9 cm2/s.

  3. Heterogeneity of chlorinated hydrocarbon sorption properties in a sandy aquifer.

    PubMed

    Zhao, Xianda; Wallace, Roger B; Hyndman, David W; Dybas, Michael J; Voice, Thomas C

    2005-08-01

    Hydraulic conductivity and sorption coefficients for chlorinated hydrocarbons (chloroform, carbon tetrachloride and tetrachloroethylene) were evaluated for 216 sediment samples collected across a 15 m transect and a 21 m depth interval in a contaminated aquifer near Schoolcraft, Michigan. Relationships between hydraulic conductivity, linear sorption partition coefficients, grain size classes, and spatial location were investigated using linear regression analysis and geostatistical techniques. Clear evidence of layering was found in sorption properties, hydraulic conductivity and grain sizes. Conductivity correlated well with grain size, as expected, but sorption varied inversely with grain size, contrary to some previous reports. No significant correlation was found between sorption properties and hydraulic conductivity. This is likely due to the unexpected presence of small amounts of highly sorptive coal-like solids, which dominate the sorption behavior but have little effect on conductivity. The results demonstrate that recent findings regarding the high sorption capacity of coal materials found in soils can exert a controlling influence on contaminant transport. Designers of in situ remediation systems should be cautioned that 1) it is not reasonable to assume that sorption capacity and hydraulic conductivity are related, 2) sorption capacity and hydraulic conductivity are critical measurements for contaminant site characterization and subsequent transport modeling, 3) estimating sorption capacity from organic carbon measurement may lead to greater errors than performing sorption isotherms, and 4) it is more important to characterize vertical heterogeneity rather than horizontal heterogeneity because both sorption and hydraulic conductivity are correlated across longer distances in the horizontal plane.

  4. Petroleum and chlorinated hydrocarbons in water from Lake Manzala and associated canals

    SciTech Connect

    Badawy, M.I.; Wahaab, R.A.; Abou Waly, H.F.

    1995-08-01

    Lake Manzala is located at the north eastern edge of Nile Delta in Egypt. It is separated from the Mediterranean sea by a sandy beach ridge. However, the lake is in connection with the sea through three opening nearby Port Said. The area of the lake is about 769 Km{sup 2} and relatively shallow with an average depth of 1.3 m. The lake is of high economic value as a natural resource, for fishery, reacreation and for migratory birds. The lake is highly polluted as it receives wastewaters discharged by several canal. The present investigation aimed to assess the residue levels of petroleum hydrocarbons, chlorinated insecticides and polychlorinated biphenyls in the lake water as well as in Hadous canal, Fariskur canal and Bahr-El-Baqar canal. 9 refs., 1 fig., 3 tabs.

  5. Assimilation of chlorinated alkanes by hydrocarbon-utilizing fungi

    SciTech Connect

    Murphy, G.L.; Perry, J.J.

    1984-12-01

    The fatty acid compositions of two filamentous fungi (Cunninghamella elegans and Penicillium zonatum) and a yeast (Candida lipolytica) were determined after the organisms were grown on 1-chlorohexadecane or 1-chlorooctadecane. These organisms utilized the chlorinated alkanes as sole sources of carbon and energy. Analyses of the fatty acids present after growth on the chlorinated alkanes indicated that 60 to 70% of the total fatty acids in C. elegans were chlorinated. Approximately 50% of the fatty acids in C. lipolytica were also chlorinated. P. zonatum contained 20% 1-chlorohexadecanoic acid after growth on either substrate but did not incorporate C/sub 18/ chlorinated fatty acids.

  6. Hydrocarbon-solvent based cleaners as replacements for chlorinated and CFC solvents

    SciTech Connect

    Schreiner, J.L.; Berlin, E.P.

    1995-12-31

    Chlorinated and CFC solvents have been used for about 30 years to remove various contaminants from products during the manufacturing process. Among the contaminants being removed are oils, greases, and waxes that have petroleum products as the base. Prior to the advent of the chlorinated solvents petroleum distillates were used for these cleaning operations. Processing improvements over the past 30 years now permit production of higher purity hydrocarbons solvents that can be used as replacements for the chlorinated and CFC solvents being phased out. These hydrocarbon solvents are well suited for removal of the various petroleum based contaminants, as one recalls the old adage {open_quotes}like dissolves like.{close_quotes}

  7. Biological monitoring of environmental contaminants: chlorinated hydrocarbons in eggs of hens.

    PubMed

    Siddiqui, M K; Saxena, M C

    1983-12-15

    High concentrations of persistent chlorinated hydrocarbon pesticide residues were detected by gas-liquid chromatography with an electron capture detector (3H), in eggs of hens collected from Lucknow under the pesticide monitoring programme. The present study reveals extremely high contamination of eggs, particularly with DDT and HCH residues. The eggs may be an important source of DDT and HCH build-up in the human body. Residue levels of p,p'-DDT and its metabolites p,p'-DDE and alpha, beta and gamma-isomers of HCH were higher in eggs of poultry-farm hens compared to those of domestic hens. Egg yolk contained higher levels compared with egg white, because of the lipophilic nature of pesticides and the high lipid content in the yolk. Average levels of total DDT and HCH residues in the yolk and white in the whole egg of a poultry-farm hen were found to be 18.5 and 4.6 micrograms respectively, whereas the average levels were 7.4 and 4.1 micrograms, respectively, in the whole egg of a domestic hen.

  8. BIOTRANSFORMATION OF MIXTURES OF CHLORINATED ALIPHATIC HYDROCARBONS BY AN ACETATE-GROWN METHANOGENIC ENRICHMENT CULTURE. (R825549C053)

    EPA Science Inventory

    Biotransformation of chlorinated aliphatic hydrocarbons under anaerobic conditions has received considerable attention due to the prevalence of these compounds as groundwater contaminants. However, information concerning the impact of mixtures of chlorinated compounds on their...

  9. Using trees to remediate groundwaters contaminated with chlorinated hydrocarbons. 1998 annual progress report

    SciTech Connect

    Strand, S.E.; Gordon, M.P.

    1998-06-01

    'Industrial practices in the past have resulted in contamination of groundwater with chlorinated hydrocarbons (CHCs) at many DOE sites, such as Hanford and Savannah River. Such contamination is a major problem because existing groundwater remediation technologies are expensive and difficult. An inexpensive method for groundwater remediation is greatly needed. Trees could be used to remediate CHC polluted groundwater at minimal cost (phytoremediation). Before phytoremediation can be extensively applied, the authors must determine the range of compounds that are attacked, the effects of metabolic products on the plants and the environment, and the effect of transpiration and concentration of CHC on uptake and metabolism. They will test the ability of hybrid poplar to take up and transform the chlorinated methanes, ethanes and ethylenes. The rate of uptake and transformation by poplar of TCE as a function of concentration in the soil, transpiration rate and illumination level will be determined. Methods will be developed to permit rapid testing of plants from contaminated sites for species able to oxidize and sequester chlorinated compounds. They will identify the nature of the bound residues of TCE metabolism in poplar. They will identify the mechanisms involved in CHC oxidation in poplar and use genetic manipulations to enhance that activity. They will introduce the genes for mammalian cytochrome P-450-IIE1, known to oxidize light CHCs such as TCE to attempt to increase the CHC metabolism capacity of poplar. The results of this research will place phytoremediation of CHCs on a firm scientific footing, allowing a rational assessment of its application to groundwater contamination. This report summarizes the results of the first 1.5 years of work on a three-year project.'

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

    PubMed

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

    2015-09-01

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

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

    PubMed

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

    2015-09-01

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

  12. Method for removing chlorine compounds from hydrocarbon mixtures

    DOEpatents

    Janoski, Edward J.; Hollstein, Elmer J.

    1985-12-31

    A process for removing halide ions from a hydrocarbon feedstream containing halogenated hydrocarbons wherein the contaminated feedstock is contacted with a solution of a suitable oxidizing acid containing a lanthanide oxide, the acid being present in a concentration of at least about 50 weight percent for a time sufficient to remove substantially all of the halide ion from the hydrocarbon feedstock.

  13. Method for removing chlorine compounds from hydrocarbon mixtures

    DOEpatents

    Janoski, E.J.; Hollstein, E.J.

    1984-09-29

    A process for removing halide ions from a hydrocarbon feedstream containing halogenated hydrocarbons wherein the contaminated feedstock is contacted with a solution of a suitable oxidizing acid containing a lanthanide oxide, the acid being present in a concentration of at least about 50 weight percent for a time sufficient to remove substantially all of the halide ion from the hydrocarbon feedstock.

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

    Technology Transfer Automated Retrieval System (TEKTRAN)

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

  15. Chlorinated Hydrocarbon Degradation in Plants: Mechanisms and Enhancement of Phytoremediation of Groundwater Contamination

    SciTech Connect

    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.

  16. Persistent pollutants: a brief history of the discovery of the widespread toxicity of chlorinated hydrocarbons.

    PubMed

    Rosner, David; Markowitz, Gerald

    2013-01-01

    Rachel Carson's Silent Spring is often depicted as the beginning of a broad societal concern about the dangers of DDT and other pesticides. Attention to the other chlorinated hydrocarbons, specifically PCBs, is seen as an outgrowth of the late 1960s environmental movement. Carson's work was clearly critical in broadening the history to include the environmental impact and set the stage for the path breaking work decades later by Theo Colburn and others on endocrine disruptions associated with other synthetic chemicals. This article reviews the development of the understanding the dangers of the chlorinated hydrocarbons in the decades preceding Carson's book. Although little noticed, Rachel Carson makes this observation herself.

  17. Formation of stable chlorinated hydrocarbons in weathering plant material

    SciTech Connect

    Myneni, Satish C. B.

    2001-10-01

    Though several chlorinated organic compounds produced by humans are carcinogenic and toxic, some are also produced by the biotic and abiotic processes in the environment. In situ x-ray spectroscopy data indicate that natural organic matter in soils, sediments, and natural waters contain stable, less volatile organic compounds with chlorinated phenolic and aliphatic groups as the principal Cl forms. These compounds are formed at rapid rates from the transformation of inorganic Cl during humification of plant material and, thus, play a critical role in the cycling of Cl and of several major and trace elements in the environment and may influence human health. [References: 19

  18. Transfer of chlorinated hydrocarbons in the food chain lichen > reindeer > man

    SciTech Connect

    Villeneuve, J.P.; Holm, E.; Cattini, C.

    1985-01-01

    Lichen Caladonia alpestris collected in the Northern part of Sweden were analyzed together with samples of reindeer and wolf living in the same area. From these results one can estimate the annual intake of these compounds by Lapplanders. The amount ingested by lapplanders is far below the maximum permissible limit set for the intake of chlorinated hydrocarbons through food.

  19. Chlorinated Hydrocarbon Degradation in Plants: Mechanisms and Enhancement of Phytoremediation of Groundwater Contamination

    SciTech Connect

    Strand, Stuart E.

    2003-06-01

    Our research objectives are as follows: (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.

  20. Modeling the national chlorinated hydrocarbon supply chain and effects of disruption.

    SciTech Connect

    Sun, Amy Cha-Tien; Downes, Paula Sue; Blair, Angela S.; Welk, Margaret Ellen

    2010-03-01

    Chlorinated hydrocarbons represent the precursors for products ranging from PVC and refrigerants to pharmaceuticals. Natural or manmade disruptions that affect the availability of these products nationally have the potential to affect a wide range of markets, from healthcare to construction. Sandia National Laboratories (Sandia) has developed datasets and models that allow the analysis of the interdependencies within the chlorine chemical supply chain and consequences of disruptions. Combining data on plant locations, transportation, utilities, and the chemical supply chain itself, with modeling tools such as N-ABLE, a Sandia-developed agent based modeling system, allows Sandia to model this complex system dynamically. Sandia has used the N-ABLE technology to simulate a disruption to the chlorinated hydrocarbon supply chain caused by a hurricane striking the Louisiana coast. This paper presents results and conclusions from this analysis.

  1. Process for solvent deasphalting of residual hydrocarbon oils

    SciTech Connect

    Auboir, P.; Bonnefond, P.; Mank, L.

    1983-07-26

    An asphaltene-containing residual hydrocarbon oil is deasphalted by means of a light hydrocarbon solvent. Heating of the resultant asphaltic phase for solvent removal is effected by heat exchange with the deasphalted oil previously subjected to sufficient heating in a furnace heated by flame. Fouling of the plant is thus avoided.

  2. Incorporation of chlorinated alkanes into fatty acids of hydrocarbon-utilizing mycobacteria.

    PubMed

    Murphy, G L; Perry, J J

    1983-12-01

    The cellular fatty acid composition of Mycobacterium vaccae JOB5 and Mycobacterium convolutum R22 was examined after growth on n-alkanes and compared with the fatty acids of the organisms after growth on 1-chlorohexadecane and 1-chlorooctadecane. Growth on n-alkanes resulted in normal fatty acid profiles. Mass spectral analyses indicated that, after growth on the terminally chlorinated n-alkanes, 75 to 86% of the fatty acids in M. convolutum and ca. 55% of the fatty acids in M. vaccae contained chlorine. Neither organism could utilize chloroacetate or 3-chloropropionate as sole source of carbon and energy. When these compounds were added to a growth medium with n-hexadecane as substrate, there was no evidence that chlorinated fatty acids were produced. Terminally chlorinated n-alkanes can be added to the list of n-alkanes, alkenes, and cyclohexylalkane derivatives that can be directly incorporated into cellular fatty acids of hydrocarbon-utilizing organisms.

  3. Assessment of degradation pathways in an aquifer with mixed chlorinated hydrocarbon contamination using stable isotope analysis.

    PubMed

    Hunkeler, Daniel; Aravena, Ramon; Berry-Spark, Karen; Cox, Evan

    2005-08-15

    The demonstration of monitored natural attenuation (MNA) of chlorinated hydrocarbons in groundwater is typically conducted through the evaluation of concentration trends and parent-daughter product relationships along prevailing groundwater flow paths. Unfortunately, at sites contaminated by mixtures of chlorinated ethenes, ethanes, and methanes, the evaluation of MNA by using solely concentration data and parent-daughter relationships can result in erroneous conclusions regarding the degradation mechanisms that are truly active at the site, since many of the daughter products can be derived from multiple parent compounds. Stable carbon isotope analysis was used, in conjunction with concentration data, to clarify and confirm the active degradation pathways at a former waste solvent disposal site where at least 14 different chlorinated hydrocarbons have been detected in the groundwater. The isotope data indicate that TCE, initially believed to be present as a disposed product and/or a PCE dechlorination intermediate, is attributable to dehydrochlorination of 1,1,2,2-PCA. The isotope data further support that vinyl chloride and ethene in the site groundwater result from dichloroelimination of 1,1,2-trichlorethane and 1,2-dichloroethane, respectively, rather than from reductive dechlorination of the chlorinated ethenes PCE, TCE, or 1,2-DCE. The isotope data confirm that the chlorinated ethanes and chlorinated methanes are undergoing significant intrinsic degradation, whereas degradation of the chlorinated ethenes may be limited. In addition to the classical trend of enriched isotope values of the parent compounds with increasing distance associated to biodegradation, shifts of isotope ratios of degradation byproduct in the opposite direction due to mixing of isotopically light byproducts of biodegradation with compounds from the source are shown to be of high diagnostic value. These data underline the value of stable isotope analysis in confirming transformation

  4. Determination of chlorinated polycyclic aromatic hydrocarbons in water by solid-phase extraction coupled with gas chromatography and mass spectrometry.

    PubMed

    Wang, Xianli; Kang, Haiyan; Wu, Junfeng

    2016-05-01

    Given the potential risks of chlorinated polycyclic aromatic hydrocarbons, the analysis of their presence in water is very urgent. We have developed a novel procedure for determining chlorinated polycyclic aromatic hydrocarbons in water based on solid-phase extraction coupled with gas chromatography and mass spectrometry. The extraction parameters of solid-phase extraction were optimized in detail. Under the optimal conditions, the proposed method showed wide linear ranges (1.0-1000 ng/L) with correlation coefficients ranging from 0.9952 to 0.9998. The limits of detection and the limits of quantification were in the range of 0.015-0.591 and 0.045-1.502 ng/L, respectively. Recoveries ranged from 82.5 to 102.6% with relative standard deviations below 9.2%. The obtained method was applied successfully to the determination of chlorinated polycyclic aromatic hydrocarbons in real water samples. Most of the chlorinated polycyclic aromatic hydrocarbons were detected and 1-monochloropyrene was predominant in the studied water samples. This is the first report of chlorinated polycyclic aromatic hydrocarbons in water samples in China. The toxic equivalency quotients of chlorinated polycyclic aromatic hydrocarbons in the studied tap water were 9.95 ng the toxic equivalency quotient m(-3) . 9,10-Dichloroanthracene and 1-monochloropyrene accounted for the majority of the total toxic equivalency quotients of chlorinated polycyclic aromatic hydrocarbons in tap water.

  5. Determination of chlorinated polycyclic aromatic hydrocarbons in water by solid-phase extraction coupled with gas chromatography and mass spectrometry.

    PubMed

    Wang, Xianli; Kang, Haiyan; Wu, Junfeng

    2016-05-01

    Given the potential risks of chlorinated polycyclic aromatic hydrocarbons, the analysis of their presence in water is very urgent. We have developed a novel procedure for determining chlorinated polycyclic aromatic hydrocarbons in water based on solid-phase extraction coupled with gas chromatography and mass spectrometry. The extraction parameters of solid-phase extraction were optimized in detail. Under the optimal conditions, the proposed method showed wide linear ranges (1.0-1000 ng/L) with correlation coefficients ranging from 0.9952 to 0.9998. The limits of detection and the limits of quantification were in the range of 0.015-0.591 and 0.045-1.502 ng/L, respectively. Recoveries ranged from 82.5 to 102.6% with relative standard deviations below 9.2%. The obtained method was applied successfully to the determination of chlorinated polycyclic aromatic hydrocarbons in real water samples. Most of the chlorinated polycyclic aromatic hydrocarbons were detected and 1-monochloropyrene was predominant in the studied water samples. This is the first report of chlorinated polycyclic aromatic hydrocarbons in water samples in China. The toxic equivalency quotients of chlorinated polycyclic aromatic hydrocarbons in the studied tap water were 9.95 ng the toxic equivalency quotient m(-3) . 9,10-Dichloroanthracene and 1-monochloropyrene accounted for the majority of the total toxic equivalency quotients of chlorinated polycyclic aromatic hydrocarbons in tap water. PMID:26960154

  6. Flux of transuranium nuclides and chlorinated hydrocarbons in the northwestern Mediterranean

    NASA Astrophysics Data System (ADS)

    Fowler, S. W.; Ballestra, S.; Villeneuve, J.-P.

    1990-09-01

    The transuranium nuclides, plutonium and americium, and selected chlorinated hydrocarbon compounds have been measured in sediment trap samples, bottom sediments and waters. These measurements have been used to quantify vertical fluxes and elucidate particulate biogeochemical cycles, of these man-made contaminants in the northwestern Mediterranean. Sediment trap experiments in the Gulf of Lions (Lacaze-Duthiers Canyon) have shown that transuranic fluxes are considerably higher in the Gulf of Lions, than those which have been reported for the northeast Pacific; principally this is due to the relatively high mass fluxes in this region of the Mediterranean. Water, surface sediment and sediment trap data indicate that 241Am is being transported downward (via particle settling) more rapidly than 239+240Pu. From direct flux measurement, residence times for 239+240Pu and 241Am in the upper 300 m were computed to be 2.5 and 0.14 years, respectively. Comparison of 239+240Pu concentrations in the water column, in 1986, with similar measurements made 5-11 years earlier suggests that fallout input to the Mediterranean has decreased by nearly a factor of 2 during the period 1975-1986. Fluxes of PCB, HCB, γ-HCH and DDT residues varied by as much as an order of magnitude, or more, both temporally and with depth. The average fluxes of most of the compounds in the Lacaze-Duthiers Canyon, during 1985-1986, were quite similar to those measured off the coast of Monaco several years earlier. Generally, the increased chlorinated hydrocarbon fluxes observed with depth were a direct result of the much higher mass fluxes which occurred at depth. Demonstrated differences in PCB concentrations in the settling particles, deposited surface sediments and overlying sediment floc indicate that simple bottom sediment resuspension is not a major contributor to the enhanced PCB flux noted at depth. The PCB concentration in sedimenting particulate material collected from deeper waters, is similar to

  7. POPULATION DIVERSITY IN MODEL DRINKING WATER BIOFILMS RECEIVING CHLORINE OR MONOCHLORAMINE RESIDUAL

    EPA Science Inventory

    Most water utilities add monochloramine or chlorine as a residual disinfectant in potable water distribution systems (WDS) to control bacterial regrowth. While monochloramine is considered more stable than chlorine, little is known about the fate of this disinfectant or the effec...

  8. ASCORBIC ACID REDUCTION ON RESIDUAL ACTIVE CHLORINE IN POTABLE WATER PRIOR TO HALOCARBOXYLATE DETERMINATION

    EPA Science Inventory

    In studies on the formation of disinfection byproducts (DBPs), it is necessary to scavenge residual active (odxidizing) chlorine in order to fix the chlorination byproducts (such as haloethanoates) at a point in time . Such research projects often have distinct needs from requi...

  9. ASCORBIC ACID REDUCTION OF RESIDUAL ACTIVE CHLORINE IN POTABLE WATER PRIOR TO HALOCARBOXYLATE DETERMINATION

    EPA Science Inventory

    In studies on the formation of disinfection byproducts (DBPs), it is necessary to scavenge residual active (oxidizing) chlorine in order to fix the chlorination byproducts (such as haloethanoates) at a point in time. Thus, methods designed for compliance monitoring are not alway...

  10. Kinetics of aerobic cometabolic biodegradation of chlorinated and brominated aliphatic hydrocarbons: A review.

    PubMed

    Jesus, João; Frascari, Dario; Pozdniakova, Tatiana; Danko, Anthony S

    2016-05-15

    This review analyses kinetic studies of aerobic cometabolism (AC) of halogenated aliphatic hydrocarbons (HAHs) from 2001-2015 in order to (i) compare the different kinetic models proposed, (ii) analyse the estimated model parameters with a focus on novel HAHs and the identification of general trends, and (iii) identify further research needs. The results of this analysis show that aerobic cometabolism can degrade a wide range of HAHs, including HAHs that were not previously tested such as chlorinated propanes, highly chlorinated ethanes and brominated methanes and ethanes. The degree of chlorine mineralization was very high for the chlorinated HAHs. Bromine mineralization was not determined for studies with brominated aliphatics. The examined research period led to the identification of novel growth substrates of potentially high interest. Decreasing performance of aerobic cometabolism were found with increasing chlorination, indicating the high potential of aerobic cometabolism in the presence of medium- and low-halogenated HAHs. Further research is needed for the AC of brominated aliphatic hydrocarbons, the potential for biofilm aerobic cometabolism processes, HAH-HAH mutual inhibition and the identification of the enzymes responsible for each aerobic cometabolism process. Lastly, some indications for a possible standardization of future kinetic studies of HAH aerobic cometabolism are provided.

  11. Kinetics of aerobic cometabolic biodegradation of chlorinated and brominated aliphatic hydrocarbons: A review.

    PubMed

    Jesus, João; Frascari, Dario; Pozdniakova, Tatiana; Danko, Anthony S

    2016-05-15

    This review analyses kinetic studies of aerobic cometabolism (AC) of halogenated aliphatic hydrocarbons (HAHs) from 2001-2015 in order to (i) compare the different kinetic models proposed, (ii) analyse the estimated model parameters with a focus on novel HAHs and the identification of general trends, and (iii) identify further research needs. The results of this analysis show that aerobic cometabolism can degrade a wide range of HAHs, including HAHs that were not previously tested such as chlorinated propanes, highly chlorinated ethanes and brominated methanes and ethanes. The degree of chlorine mineralization was very high for the chlorinated HAHs. Bromine mineralization was not determined for studies with brominated aliphatics. The examined research period led to the identification of novel growth substrates of potentially high interest. Decreasing performance of aerobic cometabolism were found with increasing chlorination, indicating the high potential of aerobic cometabolism in the presence of medium- and low-halogenated HAHs. Further research is needed for the AC of brominated aliphatic hydrocarbons, the potential for biofilm aerobic cometabolism processes, HAH-HAH mutual inhibition and the identification of the enzymes responsible for each aerobic cometabolism process. Lastly, some indications for a possible standardization of future kinetic studies of HAH aerobic cometabolism are provided. PMID:26874310

  12. Biodegradation of individual and multiple chlorinated aliphatic hydrocarbons by methane-oxidizing cultures.

    PubMed Central

    Chang, H L; Alvarez-Cohen, L

    1996-01-01

    The microbial degradation of chlorinated and nonchlorinated methanes, ethanes, and ethanes by a mixed methane-oxidizing culture grown under chemostat and batch conditions is evaluated and compared with that by two pure methanotrophic strains: CAC1 (isolated from the mixed culture) and Methylosinus trichosporium OB3b. With the exception of 1,1-dichloroethylene, the transformation capacity (Tc) for each chlorinated aliphatic hydrocarbon was generally found to be in inverse proportion to its chlorine content within each aliphatic group (i.e., methanes, ethanes, and ethenes), whereas similar trends were not observed for degradation rate constants. Tc trends were similar for all methane-oxidizing cultures tested. None of the cultures were able to degrade the fully chlorinated aliphatics such as perchloroethylene and carbon tetrachloride. Of the four cultures tested, the chemostat-grown mixed culture exhibited the highest Tc for trichloroethylene, cis-1,2-dichloroethylene, tetrachloroethane, 1,1,1-trichloroethane, and 1,2-dichloroethane, whereas the pure batch-grown OB3b culture exhibited the highest Tc for all other compounds tested. The product toxicity of chlorinated aliphatic hydrocarbons in a mixture containing multiple compounds was cumulative and predictable when using parameters measured from the degradation of individual compounds. The Tc for each chlorinated aliphatic hydrocarbon in a mixture (Tcmix) and the total Tc for the mixture (sigma Tcmix) are functions of the individual Tc, the initial substrate concentration (S0), and the first-order rate constant (k/Ks) of each compound in the mixture, indicating the importance of identifying the properties and compositions of all potentially degradable compounds in a contaminant mixture. PMID:8795228

  13. MODELING CHLORINE RESIDUALS IN DRINKING-WATER DISTRIBUTION SYSTEMS

    EPA Science Inventory

    A mass-transfer-based model is developed for predicting chlorine decay in drinking-water distribution networks. The model considers first-order reactions of chlorine to occur both in the bulk flow and at the pipe wall. The overall rate of the wall reaction is a function of the ...

  14. Mass balance studies of volatile chlorinated hydrocarbon phytoremediation.

    PubMed

    Strand, Stuart E; Dossett, Michael; Harris, Chad; Wang, Xiaoping; Doty, Sharon L

    2005-01-01

    In field-scale mass balance studies of poplar remediation of carbon tetrachloride (CT), more than 95% of the mass of CT was degraded with all of the CT chlorine accountable as chloride ion accumulation in the soil. Atmospheric loss of CT through leaf transpiration and trunk diffusion was insignificant. These findings are consistent with previously reported uptake and degradation of trichloroethylene (TCE) by poplar. Poplar phytoremediation of CT and TCE results in little decrease in aqueous concentration, since water is taken up at about the same rate as the chlorinated compounds. From this result we predict that phytoirrigation--the application of pumped contaminated groundwater to planted systems--will result in concentrations of the pollutants at the bottom of the root zone that are higher than permitted regulatory levels. Such plantations will be susceptible to loss of contaminants during rainfall events, possibly resulting in pollution of uncontaminated soil. Greenhouse studies of pollutant profiles in the media beneath poplar trees that were surface irrigated with TCE and CT confirmed that regulatory concentrations of these pollutants were not achieved in the root zone of the poplar; rather concentrations fell by less than 50%.

  15. Evaluated Enthalpies of Formation of the Stable Closed Shell C1 and C2 Chlorinated Hydrocarbons

    NASA Astrophysics Data System (ADS)

    Manion, Jeffrey A.

    2002-03-01

    Experimental data on the enthalpies of formation of chloromethanes, chloroethynes, chloroethenes, and chloroethanes are critically reviewed. Enthalpy of formation values for the C1 and C2 chlorinated hydrocarbons are highly cross-linked by various measured reaction equilibria and currently available sets of values are not internally self-consistent. It is shown that the early static bomb combustion calorimetry studies on highly chlorinated compounds generally give enthalpies of formation that are systematically more positive than later values derivable from rotating bomb combustion or equilibria studies. Those previously recommended values which were based mainly on the early static bomb work therefore need substantial revision. On the basis of more recent literature data obtained with rotating bomb combustion calorimetry, together with analyses of literature data on other reaction enthalpies and equilibria involving chlorinated hydrocarbons, an updated self-consistent set of ΔfHo[298.15 K] values for closed shell chlorinated C1 and C2 hydrocarbons (25 compounds) is recommended. Data on the enthalpies of vaporization are also reviewed and values of ΔvapH[298.15 K] and ΔvapHo[298.15 K] are recommended. The presently suggested enthalpies of formation for highly chlorinated alkenes and alkanes (particularly C2Cl4, C2HCl3, C2HCl5, and C2Cl6) are significantly (8-15 kJ mol-1) more negative than given by most previous evaluators. Values for the chloroethynes are 10-25 kJ mol-1 more positive than given in previous reviews and more limited changes are suggested for other compounds in the series.

  16. Radiation induced dechlorination of some chlorinated hydrocarbons in aqueous suspensions of various solid particles

    NASA Astrophysics Data System (ADS)

    Múčka, V.; Buňata, M.; Čuba, V.; Silber, R.; Juha, L.

    2015-07-01

    Radiation induced dechlorination of trichloroethylene (TCE) and tetrachloroethylene (PCE) in aqueous solutions containing the active carbon (AC) or cupric oxide (CuO) as the modifiers was studied. The obtained results were compared to the previously studied dechlorination of polychlorinated biphenyls (PCBs). Both modifiers were found to decrease the efficiency of dechlorination. The AC modifier acts mainly via adsorption of the aliphatic (unlike the aromatic) hydrocarbons and the CuO oxide mainly inhibits the mineralization of the perchloroethylene. The results presented in this paper will be also helpful for the studies of the impact of chlorinated hydrocarbons on the membrane permeability of living cells.

  17. Optimum energy and by-product recovery in chlorinated hydrocarbon disposal systems

    SciTech Connect

    Santoleri, J.J.

    1982-01-01

    This paper covers the three principal areas of a chlorinated hydrocarbon waste disposal system for a typical vinyl chloride monomer facility. These are the incineration, the energy recovery system, and the by-product recovery system. It is shown that the overall efficiency of the energy and by-product recovery systems is dependent on the optimization of the primary combustor (incineration system). 11 refs.

  18. Using trees to remediate groundwaters contaminated with chlorinated hydrocarbons. 1997 annual progress report

    SciTech Connect

    Gordon, M.P.; Newman, L.A.; Strand, S.E.

    1997-01-01

    'Metabolism of Chlorinated Hydrocarbons Laboratory and field tests with poplar in tissue culture, bioreactors, and field sites have shown that, unlike bacteria, these plants are able to carry out complete degradation of fully chlorinated alkanes and alkenes to carbon dioxide and chloride. Carbon dioxide was produced as a product of the degradation of trichloroethylene (TCE), carbon tetrachloride (CT), and perchloroethylene (PCE) when axenic tissue cultures of poplar cells were exposed to radiolabelled compounds. The apparent degradation of PCE and CT, fully chlorinated hydrocarbons, in these aerobic plants is remarkable when contrasted to the lack of comparable aerobic degradation by bacteria. Oxidized metabolites, such as trichloroethanol, and di- and trichloroacetic acid, were detected in cell cultures exposed to TCE, suggesting the involvement of cytochrome P450s or other monooxygenase activities. Mass balance experiments with small poplar plants in laboratory reactors showed that significant TCE and CT was volatilized from the leaves, while a similar fraction of radiolabeled carbon from these chlorinated solvents was retained in the plant tissue.'

  19. Formation of phosgene during welding activities in an atmosphere containing chlorinated hydrocarbons.

    PubMed

    Nieuwenhuizen, M S; Groeneveld, F R

    2000-01-01

    The formation of phosgene During welding activities in an atmosphere containing chlorinated hydrocarbons was investigated. Four different chlorinated hydrocarbons were studied under laboratory conditions. Results are presented as time-averaged phosgene concentration in a total volume of 250 L of air being purged through a 52-L reaction vessel during 20 min. It was found that the formation of phosgene was in the order dichloromethane < Freon-22 < carbon tetrachloride < trichoroethylene. Local concentrations may be higher depending on dispersion phenomena. The interpretation in terms of occupational health was rather difficult because of the interaction with smoke particles and because of possible nonhomogeneous dispersion of phosgene around the workers. In the case of dichloromethane and carbon tetrachloride the short-term maximum allowable concentration (MAC) of phosgene was not attained at the respective MAC values of the chlorinated hydrocarbons themselves. In the case of trichloroethylene and Freon-22, however, the short-term MAC-value of phosgene was attained even when the concentration was still much below the respective MAC-values.

  20. Membrane-Extraction Ion Mobility Spectrometry for In-Situ Detection of Chlorinated Hydrocarbons in Water

    SciTech Connect

    Du, Yongzhai; Zhang, Wei; Whitten, William B; Li, Haiyang; Watson, David B; Xu, Jun

    2010-01-01

    Membrane-extraction ion mobility spectrometry (ME-IMS) has been developed for in-situ sampling and analysis of trace chlorinated hydrocarbons in water in a single procedure. The sampling is configured so that aqueous contaminants permeate through a spiral hollow polydimethylsiloxane (PDMS) membrane and are carried away by a vapor flow through the membrane tube. The extracted analyte flows into an atmospheric pressure chemical ionization (APCI) chamber and is analyzed in a home-made IMS analyzer. PDMS membrane is found to effectively extract chlorinated hydrocarbon solvents from liquid phase to vapor. The specialized IMS analyzer has been found to have resolutions of R=33 and 41, respectively, for negative- and positive-modes and is capable of detecting aqueous tetrachloroethylene (PCE) and trichloroethylene (TCE) as low as 80 g/L and 74 g/L in negative ion mode, respectively. The time-dependent characteristics of sampling and detection of TCE are both experimentally and theoretically studied for various concentrations, membrane lengths, and flow rates. These characteristics demonstrate that membrane-extraction IMS is feasible for the continuous monitoring of chlorinated hydrocarbons in water.

  1. Polyethylene as a source of artifacts in the paper chromatography of chlorinated hydrocarbon insecticides

    USGS Publications Warehouse

    Van Valin, C.C.; Kallman, B.J.; O'Donnell, J.J

    1963-01-01

    The introduction of artifacts from vessels, materials, and chemicals is a serious problem in the study of pesticide residues. It is therefore of interest to record findings that polyethylene wash bottles contain substances soluble in organic solvents and reactive with the silver nitrate chromogenic spray commonly employed in the paper chromatographic analysis of chlorinated organic insecticides.

  2. Natural attenuation of chlorinated hydrocarbons in a freshwater wetland

    USGS Publications Warehouse

    Lora, Michelle M.; Olsen, Lisa D.; Smith, Barrett L.; Alleman, Bruce C.; Leeson, Andrea

    1997-01-01

    Natural attenuation of chlorinated volatile organic compounds (VOC's) occurs as ground water discharges from a sand aquifer to a freshwater wetland at Aberdeen Proving Ground, Md. Field and laboratory results indicate that biotransformation in the anaerobic wetland sediments is an important attenuation process. Relatively high concentrations of the parent compounds trichloroethylene (TCE) and 1,1,2,2-tetrachloroethane (PCA) and low or undetectable concentrations of daughter products were measured in the aquifer. In contrast, relatively high concentrations of the daughter products cis- and trans-1,2-dichloroethylene (12DCE); vinyl chloride (VC); 1,1,2-trichloroethane (112TCA); and 1,2-dichloroethane (12DCA) were measured in ground water in the wetland sediments, although total VOC concentrations decreased upward from about 1 mu mol/L (micromoles per liter) at the base of the wetland sediments to less than 0.2 near the surface. Microcosm experiments showed that 12DCE and VC are produced from anaerobic degradation of both TCE and PCA; PCA degradation also produced 112TCA and 12DCA.

  3. Eggshell thinning, chlorinated hydrocarbons, and mercury in inland aquatic bird eggs, 1969 and 1970

    USGS Publications Warehouse

    Faber, R.A.; Hickey, J.J.

    1973-01-01

    In the Upper Great Lakes States, 9 out of 13 species of fish-eating birds were found in 1969-70 to have sustained statistically significant decreases in eggshell thickness since 1946. Maximum changes in a thickness index occurred in great blue herons (-25%), red-breasted mergansers (-23%), common mergansers (-15%). and double-crested cormorants (-15%). Heron eggs taken in Louisiana generally displayed a smaller post-'46 change than herons in the Middle West. On a lipid basis, mean PCB- and DDE- residue levels exceeded 100 ppm in 7 out of 13 species in the Great Lakes States, and in 2 of 7 species in Louisiana, the average DDE: PCB ratios in the two regions being 1.25:1 and 3.9:1, respectively. Individual dieldrin values tended 10 be higher in Louisiana (31.6 and 13.95 ppm in heron species from two different locations), although values reached 10.1 and 9.4 ppm in great blue and black-crowned night herons in Wisconsin. BHC averaged 3.01 and 0.39 ppm in the Lake States and Louisiana, respectively. Of eggs examined for mercury. 29% had levels greater than 0.5 ppm, and 9% greater than 1.0 ppm on a wet-weight basis. Mercury levels in a small sample of eggs from Louisiana were consistently low. The differences in mercury levels between the two regions thus were similar to those found for the chlorinated hydrocarbons. While DDE was a prominent factor for most groups, especially herons, in relation to the eggshell thinning observed, dieldrin was also important to two groups even though DDE was present in much higher amounts. PCB's were also important to mergansers, while mercury was positively correlated with thickness index in grebes and negatively correlated in mergansers.

  4. Assessing breeding potential of peregrine falcons based on chlorinated hydrocarbon concentrations in prey.

    PubMed

    Elliott, J E; Miller, M J; Wilson, L K

    2005-03-01

    Peregrine falcons (Falco peregrinus) now breed successfully in most areas of North America from which they were previously extirpated. The loss during the mid-part of the last century of many of the world's peregrine populations was largely a consequence of impaired reproduction caused by the effects of DDE on eggshell quality and embryo hatchability. Population recovery has been attributed to re-introduction efforts, coupled with regulatory restrictions on the use of organochlorine pesticides. Peregrines have not returned to breed in some areas, such as the Okanagan Valley of British Columbia. That region has been extensively planted in fruit orchards which were treated annually with DDT during the early 1950s to the 1970s. Ongoing contamination of avian species, including potential peregrine prey, inhabiting orchards has been documented. In response to an initiative to release peregrines around the city of Kelowna in the Okanagan Valley, we collected potential peregrine prey species and analyzed whole bodies for chlorinated hydrocarbon residues. We used a simple bioaccumulation model to predict concentrations of DDE in peregrine eggs using concentrations in prey and estimates of dietary makeup as input. Peregrines would be expected to breed successfully only if they fed on a diet primarily of doves. Feeding on as little as 10% of other species such as starlings, robins, gulls and magpies would produce DDE concentrations in peregrine eggs greater than the threshold of 15 mg/kg. We also estimated the critical concentration of DDE in total prey to be about 0.5 mg/kg, one half of the previous most conservative criterion for peregrine prey. Concentrations of dieldrin and PCBs in peregrine prey are less than suggested critical levels.

  5. Chlorinated hydrocarbons in coastal lagoons of the pacific coast of Nicaragua.

    PubMed

    Carvalho, F P; Montenegro-Guillen, S; Villeneuve, J; Cattini, C; Bartocci, J; Lacayo, M; Cruz, A

    1999-02-01

    A screening for persistent chlorinated hydrocarbons was carried out in December 1995 in the main coastal lagoons on the Pacific side of Nicaragua, where most of the country's agriculture and pesticide use has been taking place for decades. Results for a wide range of organochlorine pesticides in lagoon sediments show levels that generally were very low in Estero Real, Estero Padre Ramos, and estuary of San Juan del Sur. For example, total DDTs in these lagoons averaged 4.5 +/- 3.4 ng g-1 dry weight, which may be considered a baseline level for the region. Other compounds such as HCHs, BHC, endosulfan, heptachlor, endrin, toxaphene, and aroclors were present in concentrations even lower, generally below 1 ng g-1 dry weight. However, sediments of the Esteros Naranjo-Paso Caballos system at Chinandega district contained pesticide residues in much higher levels, attaining maximum values of 1,420 ng g-1 and 270 ng g-1 dry weight, respectively, for toxaphene and total DDTs. Other compounds such as aroclors, chlordane, endosulfan, and dieldrin were also present in the sediments of this lagoon system, but in lower concentrations. The very high concentrations of toxaphene and DDTs in this lagoon are a result of the intensive use of these pesticides in cotton growing in the district of Chinandega. Due to the long environmental half-lives of these compounds (t(1/2) > 10 years in temperate soils), their concentrations in lagoon sediments will likely remain high for years to come. Based on these results, the development of the new shrimp farming activities in the Pacific coastal lagoons should be restricted to selected areas.

  6. Potential of non-ligninolytic fungi in bioremediation of chlorinated and polycyclic aromatic hydrocarbons.

    PubMed

    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.

  7. Stabile Chlorine Isotope Study of Martian Shergottites and Nakhlites; Whole Rock and Acid Leachates and Residues

    NASA Technical Reports Server (NTRS)

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

    2011-01-01

    We have established a precise analytical technique for stable chlorine isotope measurements of tiny planetary materials by TIMS (Thermal Ionization Mass Spectrometry) [1], for which the results are basically consistent with the IRMS tech-nique (gas source mass spectrometry) [2,3,4]. We present here results for Martian shergottites and nakhlites; whole rocks, HNO3-leachates and residues, and discuss the chlorine isotope evolution of planetary Mars.

  8. Polychlorinated biphenyls (PCB), chlorinated pesticides, and polycyclic aromatic hydrocarbons (PAHs) in environmental standard reference materials

    SciTech Connect

    Poster, D.L.; Schantz, M.M.; Parris, R.M.; Benner, B.A. Jr.; Wise, S.A.

    1995-12-31

    Standard reference materials (SRMs) are certified reference materials issued by the National Institute of Standards and Technology (NIST). Natural matrix environmental sample SRMs have been developed the Analytical Chemistry Division to assist in validating measurements for organic contaminants in the environment. Many of these are well characterized for contaminants such as polychlorinated biphenyls (PCBs), chlorinated pesticides, and polycyclic aromatic hydrocarbons (PAHs). SRM 1649, Organics in Urban Dust, is currently available with certified concentrations for 5 PAHs but because of the widespread use of this material in air pollution monitoring programs and to expand the usefulness of this material, the authors are further characterizing the material for a larger number of PAHs as well as PCBs and chlorinated pesticides. They will also soon issue a diesel particulate extract (SRM 1975) that is well characterized for PAHS, including many nitrogen substituted compounds. In addition to natural matrix materials, solutions useful for calibrating chromatographic detector response factors and retention times, and spiking sample blanks for determination of analyte recoveries, are also available. Solution SRMs currently available contain PCS congeners, chlorinated pesticides, and PAHs. New solution SRMs in preparation will contain additional chlorinated pesticides, PCB congeners (e.g., non-ortho substituted chlorobiphenyls), and perdeuterated PAHs. Recent SRM work will be presented with particular attention on the methods used for determining organic contaminant concentrations in the urban dust material and in the diesel particulate extract.

  9. Assessment of biological effects of chlorinated hydrocarbons in osprey chicks

    USGS Publications Warehouse

    Elliott, J.E.; Wilson, L.K.; Henny, Charles J.; Trudeau, Suzanne F.; Leighton, Frederick A.; Kennedy, Sean W.; Cheng, Kimberly M.

    2001-01-01

    Osprey (Pandion haliaetus) eggs were collected during 1995 and 1996 at seven sites along the Fraser and Columbia River systems of British Columbia, Canada, and Washington and Oregon, USA. Fifty-four eggs were placed into a laboratory incubator. Thirty-eight of the hatched chicks were sacrificed within 24 h. Hatching success did not differ among sites and therefore between treatment and reference areas. Residual yolk sacs of eggs collected downstream of the large bleached-kraft pulp mill at Castlegar contained greater mean concentrations of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD, 2,930 ng/kg lipid) compared with reference sites such as the Nechako River, an upper tributary of the Fraser system (33.7 ng/kg). Total polychlorinated biphenyls (PCBs) in yolk sacs were also higher at Castlegar and in samples from the Columbia River downstream of Portland, Oregon, compared with those from the Nechako River. Concentrations of measured chemicals, including TCDD toxic equivalents (TEQs), total PCBs, p,pa??-dichlorodiphenylethylene (p,pa??-DDE), and other organochlorines were not different in eggs that failed to hatch compared with calculated whole-egg values for hatched eggs. There were significant biochemical responses; a hepatic cytochrome P4501A (CYP1A) cross-reactive protein was detected in all samples tested and correlated positively with ethoxyresorufin o-deethylase (EROD) activity and yolk sac concentrations of TEQs and total PCBs. Tissue concentrations of vitamin A compounds varied among sites and correlated positively with yolk sac concentrations of TEQs and PCBs. Morphological, histological, and other physiological parameters, including chick growth, edema, deformities, and hepatic and renal porphyrin concentrations, neither varied among sites nor showed concentration-related effects.

  10. Chloroxyanion residue quantification in cantaloupes treated with chlorine dioxide gas

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Previous studies show that treatment of cantaloupes with chlorine dioxide (ClO2) gas at 5 mg/L for 10 minutes, results in a significant reduction (p<0.05) in initial microflora, an increase in shelf life without any alteration in color, and a 4.6 and 4.3 log reduction of E. coli O157:H7 and L. monoc...

  11. Determination of residual chlorine in greywater using o-tolidine.

    PubMed

    March, J G; Gual, M; Simonet, B M

    2002-11-12

    The determination of chlorine with o-tolidine in greywater has been studied, and a batch method and a sequential injection method have been proposed. It was found that the reaction of o-tolidine with chlorine was slower in a greywater matrix. Grey water samples must be filtered before analysis, or alternatively, a blank of sample must be measured. The samples are very unstable, and after 2 h of storage in dark conditions at 4 degrees C the chlorine concentration can diminish. The standard addition method, in some samples gave unsatisfactory results as a consequence of matrix effects. It was concluded that samples with a total organic carbon (TOC) higher than 60 mgCl(-1) can not be accurately analysed using these methods. However, samples with a TOC lower than 60 mgCl(-1) gave 100+/-3% recoveries. The linear range of the methods was 0-3.0 and 0-5.0 mgCl(2)l(-1), and the limit of quantification 0.2 and 0.5 mgCl(2)l(-1), for the batch method and the sequential injection method, respectively. This is the first paper devoted to grey water from the analytical chemistry point of view.

  12. Chlorine-hydrocarbon photochemistry in the marine troposphere and lower stratosphere

    NASA Technical Reports Server (NTRS)

    Singh, H. B.; Kasting, J. F.

    1988-01-01

    The role of chlorine atoms in the oxidation of methane and nonmethane hydrocarbons (NMHCs) in the marine troposphere and lower stratosphere was investigated using a one-dimensional photochemical model that incorporated the chemistry of CH4, NMHCs, NO(x), O(x), and HO(x), as well as organic and inorganic halogens in the troposphere and lower stratosphere. The model predicted that chlorine atoms are present in the marine troposphere at the concentrations of about 1000/cu cm, mostly as a product of the reaction between OH and HCl released from sea spray. The results indicate that Cl atoms cause 20 to 40 percent of NMHC oxidation in the troposphere and 40 to 90 percent in the lower stratosphere. At 15 km, the NMHC-Cl reactions account for nearly 80 percent of the PAN produced. Where available, experimental data confirmed the model predictions.

  13. Natural attenuation of chlorinated solvents, petroleum hydrocarbons, and other organic compounds

    SciTech Connect

    Alleman, B.C.; Leeson, A.

    1999-11-01

    The natural attenuation option is getting more attention from site managers and regulators as a viable alternative to more costly engineered site remediation approaches. Natural attenuation was first demonstrated at sites with hydrocarbon contamination, but recent studies at sites contaminated by chlorinated compounds have shown that this approach often has merit for these more challenging contamination problems. Covering natural attenuation in media ranging from deep aquifers to shallow soils, and for contaminants ranging from fuels to solvents to herbicides, this volume offers the reader a comprehensive overview of case studies that represent the current state of the art in natural attenuation approaches to site remediation.

  14. Cl app: android-based application program for monitoring the residue chlorine in water

    NASA Astrophysics Data System (ADS)

    Intaravanne, Yuttana; Sumriddetchkajorn, Sarun; Porntheeraphat, Supanit; Chaitavon, Kosom; Vuttivong, Sirajit

    2015-07-01

    A farmer usually uses a cheap chemical material called chlorine to destroy the cell structure of unwanted organisms and remove some plant effluents in a baby shrimp farm. A color changing of the reaction between chlorine and chemical indicator is used to monitor the residue chlorine in water before releasing a baby shrimp into a pond. To get rid of the error in color reading, our previous works showed how a smartphone can be functioned as a color reader for estimating the chlorine concentration in water. In this paper, we show the improvement of interior configuration of our prototype and the distribution to several baby shrimp farms. In the future, we plan to make it available worldwide through the online market as well as to develop more application programs for monitoring other chemical substances.

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

    NASA Astrophysics Data System (ADS)

    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

  16. USING REDUCING AGENTS TO ELIMINATE CHLORINE DIOXIDE AND CHLORITE ION RESIDUALS IN DRINKING WATER

    EPA Science Inventory

    In an effort to determine the viability of various disinfection alternatives, the Evansville, Ind. Water and Sewer Utility is engaged in a pilot-plant investigation to compare chlorine dioxide and ozone pretreatment. As a result of increased speculation that the total residual c...

  17. Effect of reduced iron on the degradation of chlorinated hydrocarbons in contaminated soil and ground water: A review of publications

    NASA Astrophysics Data System (ADS)

    Vodyanitskii, Yu. N.

    2014-02-01

    Chlorinated hydrocarbons are among the most hazardous organic pollutants. The traditional remediation technologies, i.e., pumping of contaminated soil- and groundwater and its purification appear to be costly and not very efficient as applied to these pollutants. In the last years, a cheaper method of destroying chlorine-replaced hydrocarbons has been used based on the construction of an artificial permeable barrier, where the process develops with the participation of in situ bacteria activated by zerovalent iron. The forced significant decrease in the redox potential (Eh) down to -750 mV provides the concentration of electrons necessary for the reduction of chlorinated hydrocarbons. A rise in the pH drastically accelerates the dechlorination process. In addition to chlorine-organic compounds, ground water is often contaminated with heavy metals. The influence of the latter on the effect of zerovalent iron may be different: both accelerating its degradation (Cu) and inhibiting it (Cr). Most of the products of zerovalent iron corrosion, i.e., green rust, magnetite, ferrihydrite, hematite, and goethite, weaken the efficiency of the Fe0 barrier by mitigating the dechlorination and complicating the water filtration. However, pyrrhotite FeS, on the contrary, accelerates the dechlorination of chlorine hydrocarbons.

  18. Determination of Chlorinated Hydrocarbons in Water Using Highly Sensitive Mid-Infrared Sensor Technology

    NASA Astrophysics Data System (ADS)

    Lu, Rui; Mizaikoff, Boris; Li, Wen-Wei; Qian, Chen; Katzir, Abraham; Raichlin, Yosef; Sheng, Guo-Ping; Yu, Han-Qing

    2013-08-01

    Chlorinated aliphatic hydrocarbons and chlorinated aromatic hydrocarbons (CHCs) are toxic and carcinogenic contaminants commonly found in environmental samples, and efficient online detection of these contaminants is still challenging at the present stage. Here, we report an advanced Fourier transform infrared spectroscopy-attenuated total reflectance (FTIR-ATR) sensor for in-situ and simultaneous detection of multiple CHCs, including monochlorobenzene, 1,2-dichlorobenzene, 1,3-dichlorobenzene, trichloroethylene, perchloroethylene, and chloroform. The polycrystalline silver halide sensor fiber had a unique integrated planar-cylindric geometry, and was coated with an ethylene/propylene copolymer membrane to act as a solid phase extractor, which greatly amplified the analytical signal and contributed to a higher detection sensitivity compared to the previously reported sensors. This system exhibited a high detection sensitivity towards the CHCs mixture at a wide concentration range of 5~700 ppb. The FTIR-ATR sensor described in this study has a high potential to be utilized as a trace-sensitive on-line device for water contamination monitoring.

  19. Determination of Chlorinated Hydrocarbons in Water Using Highly Sensitive Mid-Infrared Sensor Technology

    PubMed Central

    Lu, Rui; Mizaikoff, Boris; Li, Wen-Wei; Qian, Chen; Katzir, Abraham; Raichlin, Yosef; Sheng, Guo-Ping; Yu, Han-Qing

    2013-01-01

    Chlorinated aliphatic hydrocarbons and chlorinated aromatic hydrocarbons (CHCs) are toxic and carcinogenic contaminants commonly found in environmental samples, and efficient online detection of these contaminants is still challenging at the present stage. Here, we report an advanced Fourier transform infrared spectroscopy-attenuated total reflectance (FTIR-ATR) sensor for in-situ and simultaneous detection of multiple CHCs, including monochlorobenzene, 1,2-dichlorobenzene, 1,3-dichlorobenzene, trichloroethylene, perchloroethylene, and chloroform. The polycrystalline silver halide sensor fiber had a unique integrated planar-cylindric geometry, and was coated with an ethylene/propylene copolymer membrane to act as a solid phase extractor, which greatly amplified the analytical signal and contributed to a higher detection sensitivity compared to the previously reported sensors. This system exhibited a high detection sensitivity towards the CHCs mixture at a wide concentration range of 5~700 ppb. The FTIR-ATR sensor described in this study has a high potential to be utilized as a trace-sensitive on-line device for water contamination monitoring. PMID:23982222

  20. Chlorinated and polycyclic aromatic hydrocarbons in riverine and estuarine sediments from Pearl River Delta, China.

    PubMed

    Mai, Bi-Xian; Fu, Jia-Mo; Sheng, Guo-Ying; Kang, Yue-Hui; Lin, Zheng; Zhang, Gan; Min, Yu-Shuan; Zeng, Eddy Y

    2002-01-01

    Spatial distribution of chlorinated hydrocarbons [chlorinated pesticides (CPs) and polychlorinated biphenyls (PCBs)] and polycyclic aromatic hydrocarbons (PAHs) was measured in riverine and estuarine sediment samples from Pearl River Delta, China, collected in 1997. Concentrations of CPs of the riverine sediment samples range from 12 to 158 ng/g, dry weight, while those of PCBs range from 11 to 486 ng/g. The CPs concentrations of the estuarine sediment samples are in the range 6-1658 ng/g, while concentrations of PCBs are in the range 10-339 ng/g. Total PAH concentration ranges from 1168 to 21,329 ng/g in the riverine sediment samples, whereas the PAH concentration ranges from 323 to 14,812 ng/g in the sediment samples of the Estuary. Sediment samples of the Zhujiang River and Macao harbor around the Estuary show the highest concentrations of CPs, PCBs, and PAHs. Possible factors affecting the distribution patterns are also discussed based on the usage history of the chemicals, hydrologic condition, and land erosion due to urbanization processes. The composition of PAHs is investigated and used to assess petrogenic, combustion and naturally derived PAHs of the sediment samples of the Pearl River Delta. In addition, the concentrations of a number of organic compounds of the Pearl River Delta samples indicate that sediments of the Zhujiang river and Macao harbor are most likely to pose biological impairment.

  1. Transport Modeling of Membrane Extraction of Chlorinated Hydrocarbon from Water for Ion Mobility Spectrometry

    SciTech Connect

    Zhang, Wei; Du, Yongzhai; Feng, Zhili; Xu, Jun

    2010-01-01

    Membrane-extraction Ion Mobility Spectrometry (ME-IMS) is a feasible technique for the continuous monitoring of chlorinated hydrocarbons in water. This work studies theoretically the time-dependent characteristics of sampling and detection of trichloroethylene (TCE). The sampling is configured so that aqueous contaminants permeate through a hollow polydimethylsiloxane (PDMS) membrane and are carried away by a transport gas flowing through the membrane tube into IMS analyzer. The theoretical study is based on a two-dimensional transient fluid flow and mass transport model. The model describes the TCE mixing in the water, permeation through the membrane layer, and convective diffusion in the air flow inside membrane tube. The effect of various transport gas flow rates on temporal profiles of IMS signal intensity is investigated. The results show that fast time response and high transport yield can be achieved for ME-IMS by controlling the flow rate in the extraction membrane tube. These modeled time-response profiles are important for determining duty cycles of field-deployable sensors for monitoring chlorinated hydrocarbons in water.

  2. Determination of an acceptable assimilable organic carbon (AOC) level for biological stability in water distribution systems with minimized chlorine residual.

    PubMed

    Ohkouchi, Yumiko; Ly, Bich Thuy; Ishikawa, Suguru; Kawano, Yoshihiro; Itoh, Sadahiko

    2013-02-01

    There is considerable interest in minimizing the chlorine residual in Japan because of increasing complaints about a chlorinous odor in drinking water. However, minimizing the chlorine residual causes the microbiological water quality to deteriorate, and stricter control of biodegradable organics in finished water is thus needed to maintain biological stability during water distribution. In this investigation, an acceptable level of assimilable organic carbon (AOC) for biologically stable water with minimized chlorine residual was determined based on the relationship between AOC, the chlorine residual, and bacterial regrowth. In order to prepare water samples containing lower AOC, the fractions of AOC and biodegradable organic matter (BOM) in tap water samples were reduced by converting into biomass after thermal hydrolysis of BOM at alkaline conditions. The batch-mode incubations at different conditions of AOC and chlorine residual were carried out at 20 °C, and the presence or absence of bacterial regrowth was determined. The determined curve for biologically stable water indicated that the acceptable AOC was 10.9 μg C/L at a minimized chlorine residual (0.05 mg Cl(2)/L). This result indicated that AOC removal during current water treatment processes in Japan should be significantly enhanced prior to minimization of the chlorine residual in water distribution.

  3. Determination of the Sources of Chlorinated Hydrocarbons Detected During MSL Missions

    NASA Astrophysics Data System (ADS)

    Buch, Arnaud; Belmahdi, Imène; Szopa, Cyril; Freissinet, Caroline; Glavin, Danny P.; Miller, Kirsten; Summons, Roger; Francois, Pascaline; Coll, Patrice; Eigenbrode, Jennifer; Teinturier, Samuel; Navarro-Gonzalez, Rafael; Stern, Jennifer; McAdam, Amy; Dequaire, Tristan; Millan, Maeva; Bonnet, Jean Yves; Coscia, David; Cabane, Michel; Mahaffy, Paul

    2015-04-01

    Sample Analysis at Mars (SAM) is one of the instruments of the MSL mission. Three analytical instruments composed SAM: the Tunable Laser Spectrometer (TLS), the Gas Chromatography (GC) and the Mass Spectrometer (QMS). It includes a sample preparation and gas processing system implemented with a pyrolysis system, wet chemistry (MTBSTFA and TMAH) and the hydrocarbon trap (silica beads, Tenax® TA and Carbosieve G), employed to concentrate volatiles released from the sample prior to GC-MS analysis [1]. This study investigates several propositions for chlorinated hydrocarbon formation, detected by SAM. Here we report on the detection of chlorohydrocarbon compounds and their potential origin. To date, SAM has detected a range of diverse chlorinated hydrocarbons from GCMS analysis of samples collected at the several locations explored by Curiosity (Rocknest, John Klein, Cumberland and Confidence Hill). Some of these chlorohydrocarbons are produced during pyrolysis by the reaction of Martian oxychlorine compounds in the samples with terrestrial carbon from a derivatization agent (MTBSTFA) present in SAM [2, 3]. Chlorobenzene cannot be formed by the reaction of MTBSTFA and perchlorates (2) and two other reaction pathways were therefore proposed : (i) reactions between the volatile thermal degradation products of perchlorates (e.g. O2, Cl2 and HCl) and Tenax® and (ii) the interaction of perchlorates (T > 200 °C) with OM from Martian soil such as benzenecarboxylates [4, 5]. References: 1. P. R. Mahaffy et al. (2012) Space Sci. Rev. 170, 401-478. 2. D. P. Glavin et al.(2013) JGR 118, 1955-1973. 3. L. a Leshin et al. (2013) Science 341, 1238937. 4. C. Freissinet et al. (2014) LPSC XXXXV Abstract 2796. 5. H. Steininger et al. (2012) Planet. Space Sci. 71, 9-17.

  4. Chlorinated pesticide residues in sediments from the Arabian Sea along the central west coast of India

    SciTech Connect

    Sarkar, A.; Gupta, R.S.

    1987-12-01

    The problem of environmental contamination by persistent chlorinated pesticides still evokes major concern due to the presence of their residues in the environment and in human tissues. In developing countries like India organochlorine insecticides, especially DDT are extensively being used in agriculture and vector control programs. Few data are available on their levels of concentration from the seas around India. Persistent pesticides residues can be expected to accumulate in marine sediments. However, very little data on this are available along the Indian coast. An attempt has been made in the present communication to identify and quantify some of the chlorinated pesticides residues in the marine sediments collected from different region along the central west coast of India. This is a part of our ongoing project to monitor and map pollutants within the exclusive economic zone of India.

  5. The Influence of Silica on the Reactivity of Iron Towards Chlorinated Hydrocarbons

    NASA Astrophysics Data System (ADS)

    Kohn, T.; Himmelheber, D. W.; Vikesland, P. J.; Fairbrother, D.; Roberts, A.

    2001-12-01

    Previous work has illustrated that dissolved silica present in groundwater can adsorb onto the iron media of a permeable reactive barrier. To date, little is known about the effect of adsorbed silica on the reactivity of iron towards chlorinated contaminants. Silica is a known corrosion inhibitor, and therefore silica sorption may affect the reactivity of cast iron towards redox-active species such as chlorinated ethanes. To determine the effect of silica sorption on iron reactivity towards chlorinated hydrocarbons, it is necessary to examine contaminant degradation rates under conditions where silica adsorption has been carefully accounted for. In this study we couple measurements of chlorinated hydrocarbon (CHC) (either trichloroethane (TCA) or trichloroethene) degradation rates with measurements of silica surface content. Both batch and columns studies were conducted as part of this effort. Batch studies were performed using electrolytic iron powder or iron coupons (1 cm2) in solutions containing sodium metasilicate and TCA. To evaluate the potential long-term effect of silica sorption, columns packed with untreated sieved Master Builder's iron were fed with simulated groundwater containing low levels of sodium metasilicate and chlorinated hydrocarbons (CHCs). Batch studies showed that at pH 8.5 the rate of TCA degradation decreased significantly with increasing silica concentration. Silica concentrations of 50 mg/L or more led to a two-fold decrease in the reaction rate, and a shift in the distribution of the reaction products towards less chlorinated compounds was observed. This shift could also be discerned at pH 7.5, even though the overall reaction rates were unaffected by the presence of silica. We ascribe the loss of reactivity at pH 8.5 but not at pH 7.5 to the fact that silica adsorbs onto iron more readily at higher pH. A decrease in iron reactivity towards CHCs was also observed in column experiments. Addition of silica to the feed resulted in

  6. Chlorinated hydrocarbon contaminants in feces of river otters from the southern Pacific coast of Canada, 1998-2004.

    PubMed

    Elliott, John E; Guertin, Daniel A; Balke, Jennifer M E

    2008-07-01

    Chlorinated hydrocarbon contaminants in coastal river otters (Lontra canadensis) were evaluated by sampling feces (scats) collected on the south coast of British Columbia, Canada. A broad survey of industrialized areas of the Strait of Georgia region was conducted in 1998, and a subsequent survey of working harbours in 2004. Samples from 1998 were analyzed for polychlorinated biphenyls (PCBs), organochlorine (OC) pesticides, and polychlorinated dioxins (PCDDs) and furans (PCDFs), while in 2004, chemistry was confined to summation operatorPCBs and OC pesticides. Concentrations of OC pesticides were low in both years, with only dichlorodiphenyldichloroethylene (DDE; range: 0.01-2.12 mg/kg lw) and hexachlorocyclobenzene (HCB; range: 0.003-0.25 mg/kg lw) detected in all samples. In 1998, octachlorodibenzo-p-dioxin (OCDD) and other higher chlorinated PCDD/Fs were found in most samples, with OCDD ranging from 120 ng/kg lw in Clayoquot Sound to 19,100 ng/kg lw in a pooled sample from two latrines in Nanaimo. PCBs were present in all samples. In 1998 geometric mean concentrations of the sum of 59 PCB congeners ranged from 0.49 mg/kg lw in Nanaimo to 12.3 mg/kg lw in Victoria Harbour. Six years later, mean summation operatorPCBs remained elevated (geometric mean 9.5 mg/kg lw) in Victoria Harbour. Geometric mean concentrations of summation operatorPCBs from Victoria Harbour in 1998 and 2004 were >9 mg/kg lw, a published adverse effect level for reproduction. At some latrines in both Victoria and Esquimalt Harbours, concentrations of TCDD-toxic equivalents exceeded 1500 ng/kg lw, a value for health effects in otters that we derived using published information. As shown in previous studies, analysis of scats provides an efficient and non-intrusive approach to assessing contaminant threats to otter populations, and to documenting spatial trends in residues.

  7. Toxic effects of residual chlorine on larvae of Hydropsyche pellucidula (Trichoptera, Hydropsychidae): A proposal of biological indicator

    SciTech Connect

    Camargo, J.A. )

    1991-08-01

    Elemental chlorine (Cl{sub 2}) and other chlorine compounds, such as chloramines and hypochlorites, have been used as important bactericides in disinfection of drinking waters for many years. Residual chlorine concentrations in municipal water supplies are normally between 0.5 and 2 mg/L. In water at pH values above 5, elemental chlorine and hypochlorite compounds react rapidly, resulting in the formation of hypochlorous acid (HOCl) in equilibrium with hypochlorite ions (OCL-). Very little is known about the toxicity of residual chlorine on aquatic insects that comprise the macroinvertebrate communities of freshwater ecosystems. This study examines the toxic effects of municipal chlorinated waters on larvae of Hydropsyche pellucidula (Curtis), a common insect species in macrobenthic communities of rivers and streams in the Iberian Peninsula and other European countries, evaluating implications on their life cycles. Field and laboratory studies were performed in order to reach these goals.

  8. PERMEABLE REACTIVE SUBSURFACE BARRIERS FOR THE INTERCEPTION AND REMEDIATION OF CHLORINATED HYDROCARBON AND CHROMIUM (VI) PLUMES IN GROUND WATER

    EPA Science Inventory

    This document concerns the use of permeable reactive subsurface barriers for the remediation of plumes of chlorinated hydrocarbons and Cr(VI) species in ground water, using zero-valent iron (Fe0) as the reactive substrate. Such systems have undergone thorough laboratory research,...

  9. Chlorine

    Integrated Risk Information System (IRIS)

    Chlorine ; CASRN 7782 - 50 - 5 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic Effects

  10. Chlorine

    ERIC Educational Resources Information Center

    Young, Jay A.

    2004-01-01

    A chemical laboratory information profile (CLIP) of the chemical chlorine, produced in small quantities in the laboratory, is presented. The profile summarizes physical and harmful properties, exposure limits, reactivity risks, and symptoms of major exposure for the benefit of teachers and students using the chemical in the laboratory.

  11. Evidence for Perchlorates and the Origin of Chlorinated Hydrocarbons Detected by SAM at the Rocknest Aeolian Deposit in Gale Crater

    NASA Technical Reports Server (NTRS)

    Glavin, Daniel P.; Freissinet, Caroline; Miller, Kristen E.; Eigenbrode, Jennifer L.; Brunner, Anna E.; Buch, Arnaud; Sutter, Brad; Archer, P. Douglas, Jr.; Atreya, Sushil K.; Brinckerhoff, William B.; Cabane, Michel; Coll, Patrice; Conrad, Pamela G.; Coscia, David; Dworkin, Jason P.; Franz, Heather B.; Grotzinger, John P.; Leshin, Laurie A.; Martin, Mildred G.; McKay, Christopher; Ming, Douglas W.; Navarro-Gonzalez, Rafael; Pavlov, Alexander; Steele, Andrew; Summons, Roger E.; Szopa, Cyril; Teinturier, Samuel; Mahaffy, Paul R.

    2013-01-01

    A single scoop of the Rocknest aeolian deposit was sieved (less than 150 micrometers), and four separate sample portions, each with a mass of approximately 50 mg, were delivered to individual cups inside the Sample Analysis at Mars (SAM) instrument by the Mars Science Laboratory rover's sample acquisition system. The samples were analyzed separately by the SAM pyrolysis evolved gas and gas chromatograph mass spectrometer analysis modes. Several chlorinated hydrocarbons including chloromethane, dichloromethane, trichloromethane, a chloromethylpropene, and chlorobenzene were identified by SAM above background levels with abundances of approximately 0.01 to 2.3 nmol. The evolution of the chloromethanes observed during pyrolysis is coincident with the increase in O2 released from the Rocknest sample and the decomposition of a product of N-methyl-N-(tert-butyldimethylsilyl)-trifluoroacetamide (MTBSTFA), a chemical whose vapors were released from a derivatization cup inside SAM. The best candidate for the oxychlorine compounds in Rocknest is a hydrated calcium perchlorate (Ca(ClO4)2·nH2O), based on the temperature release of O2 that correlates with the release of the chlorinated hydrocarbons measured by SAM, although other chlorine-bearing phases are being considered. Laboratory analog experiments suggest that the reaction of Martian chlorine from perchlorate decomposition with terrestrial organic carbon from MTBSTFA during pyrolysis can explain the presence of three chloromethanes and a chloromethylpropene detected by SAM. Chlorobenzene may be attributed to reactions of Martian chlorine released during pyrolysis with terrestrial benzene or toluene derived from 2,6-diphenylphenylene oxide (Tenax) on the SAM hydrocarbon trap. At this time we do not have definitive evidence to support a nonterrestrial carbon source for these chlorinated hydrocarbons, nor do we exclude the possibility that future SAM analyses will reveal the presence of organic compounds native to the

  12. Chlorinated Hydrocarbon Degradation in Plants: Mechanisms and Enhancement of Phytoremediation of Groundwater Contamination

    SciTech Connect

    Strand, Stuart E.

    2002-06-01

    Several varieties of transgenic poplar containing cytochrome P-450 2E1 have been constructed and are undergoing tests. Strategies for improving public acceptance and safety of transgenic poplar for chlorinated hydrocarbon phytoremediation are being developed. We have discovered a unique rhizobium species that lives within the stems of poplar and we are investigating whether this bacterium contributes nitrogen fixed from the air to the plant and whether this endophyte could be used to introduce genes into poplar. Studies of the production of chloride ion from TCE have shown that our present P-450 constructs did not produce chloride more rapidly than wild type plants. Follow-up studies will determine if there are other rate limiting downstream steps in TCE metabolism in plants. Studies of the metabolism of carbon tetrachloride in poplar cells have provided evidence that the native plant metabolism is due to the activity of oxidative enzymes similar to the mammalian cytochrome P-450 2E1.

  13. Role of plant biomass in the global environmental partitioning of chlorinated hydrocarbons

    SciTech Connect

    Calamari, D.; Morosini, M.; Vighi, M. ); Bacci, E.; Focardi, S.; Gaggi, C. )

    1991-08-01

    Plant biomass plays a significant role in the global environmental partitioning phenomena and plants are good indicators of tropospheric contamination levels by chlorinated hydrocarbons. In the present research 300 samples of plants were collected in 265 areas distributed worldwide and analyzed for HCB (hexachlorobenzene), {alpha}-HCH (hexachlorocyclohexane), {gamma}-HCH, p,p{prime}-DDT,o,p{prime}-DDT, and p,p{prime}-DDE (degradation product of DDT). Global HCB distribution is strongly dependent on the temperature, the HCB being present mainly in samples from cold areas. The sum of DDTs show higher concentrations in samples from topical areas, while the sum of HCHs is higher in the plants from the Northern Hemisphere. These results are discussed, taking into account the role of physicochemical properties in determining the global distribution as well as the air age of the contamination.

  14. Comparative bioaccumulation of chlorinated hydrocarbons from sediment by two infaunal invertebrates

    SciTech Connect

    Meador, J.P.; Adams, N.G.; Casillas, E.; Bolton, J.L.

    1995-12-31

    Bioaccumulation of chlorinated hydrocarbons (CHs) from field-contaminated sediments by two infaunal invertebrates, Rhepoxynius abronius and Armandia brevis was examined in the laboratory. Sediments were selected over a large geographical area of an urban estuary, the Hudson-Raritan, to assess the potential for bioaccumulation. Amphipod and polychaete tissue burdens were highly correlated over sites; however, concentrations of the trichlorobiphenyls in the polychaete were about twice that found in the amphipod and 4 to 8 times higher for the more hydrophobic PCBs. Unlike PAHs from these sediments, concentrations of CHs in IW and sediment indicated that partition coefficients (K{sub oc}) were generally as predicted. K{sub oc} values determined with non-sorbed interstitial water concentrations (IW{sub free}) were much closer to predicted values compared to those based on the total chlorinated compound. As expected, BAF values were highly variable among sites and increased greatly with declining TOC content. The BAF{sub loc} (lipid/organic carbon normalized bioaccumulation factor) for trichlorobiphenyls in the polychaete was similar to that for the amphipod; however the polychaete BAF{sub loc} increased with increasing hydrophobicity and was maximum for the pentachlorobiphenyls and close to the expected maximum. Some evidence for site-specific BAF{sub loc} values was found because of a strong correlation between BAF{sub loc} and sediment concentration; however for some PCBs, this correlation was weak.

  15. Chlorine

    SciTech Connect

    Talmage, Sylvia Smith

    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

  16. Relative induction of a biomarker, P450 RGS, by PAHs and chlorinated hydrocarbons

    SciTech Connect

    Bothner, K.; Anderson, J. |

    1995-12-31

    A reporter gene system (RGS) assay has been engineered from a human liver cancer cell fine so that the induction of CPA gene will result in the production of luciferase (firefly plasmid) instead of cytochrome P450. Induction of this test system by compounds such as polycyclic aromatic hydrocarbons (PAHs) and chlorinated hydrocarbons infers these xenobiotics are present at levels that are potentially toxic, carcinogenic, or mutagenic to organisms. Six well plates with 1.0 {times} 10{sup 6} adhered cells in 2 mLs of media are inoculated with varying volumes of organic solvents containing a reference toxicant (TCDD) and sample extracts. Solvent extracts (EPA 3540) of aquatic sediments, soils, and mussel tissue have been applied directly to this system. Test results show a significant RGS induction from concentrations of PAHs, that if present in a 40 gram sediment sample, would be (in ng/g or ppb): 20 for dibenz(a,h)anthracene; 70 for benz(a)anthracene; 100 for benzo(a)pyrene; and 250 for chrysene. Testing with mixtures of PAHs and environmental samples has shown that levels of 300 to 400 ppb are detected. Results to be presented from P450 RGS testing will show that the estimated health risk (Toxic Equivalent Factors, TEFs) of some of the PAHs may be as great or greater than some of the coplanar PCB.

  17. Crossflow air stripping and catalytic oxidation of chlorinated hydrocarbons from groundwater

    SciTech Connect

    Gavaskar, A.R.; Kim, B.C.; Rosansky, S.H.; Ong, S.K.; Marchand, E.G.

    1995-02-01

    This paper describes air stripping of chlorinated hydrocarbon contaminants from groundwater in a crossflow air stripping tower and destruction of the organic compounds by catalytic oxidation. Crossflow stripping has an advantage over conventional countercurrent stripping. In typical stripping operations, the mass transfer coefficient is insensitive to the velocity of the gas stream. The crossflow stripping tower is a geometry that increases the cross section of gas flow while making minimal disturbances to the liquid flow, allowing high gas-liquid ratios without flooding. By increasing the flow cross section for the gas stream, pressure drop (and thus fan power) can be reduced significantly. A field demonstration of the crossflow column was performed at a contaminated groundwater site. The groundwater was pumped out and sent to two 17-ft-high (5.2-m) towers in a parallel arrangement. One tower was a crossflow air stripper and the other a conventional countercurrent design. The performance of the two was compared. The key organic species targeted was dichloroethane, which has a low Henry`s law constant. Three different baffle configurations were tested in the crossflow tower. The results of this demonstration were used to develop design criteria for crossflow air strippers to be used for destruction of halogenated hydrocarbons. 4 refs., 15 figs., 2 tabs.

  18. BENZENE AND NAPHTHALENE SORPTION ON SOIL CONTAMINATED WITH HIGH MOLECULAR WEIGHT RESIDUAL HYDROCARBONS FROM UNLEADED GASOLINE

    EPA Science Inventory

    For complex nonaqueous phase liquids (NAPLs), the composition of the NAPL retained in the pore space of geologic material weathers until the residual NAPL no longer acts a liquid and exists as discrete regions of hydrocarbon (termed residual hydrocarbons) in association with the ...

  19. Microbial diversity in a hydrocarbon- and chlorinated-solvent- contaminated aquifer undergoing intrinsic bioremediation

    USGS Publications Warehouse

    Dojka, M.A.; Hugenholtz, P.; Haack, S.K.; Pace, N.R.

    1998-01-01

    A culture-independent molecular phylogenetic approach was used to survey constituents of microbial communities associated with an aquifer contaminated with hydrocarbons (mainly jet fuel) and chlorinated solvents undergoing intrinsic bioremediation. Samples were obtained from three redox zones: methanogenic, methanogenic-sulfate reducing, and iron or sulfate reducing. Small-subunit rRNA genes were amplified directly from aquifer material DNA by PCR with universally conserved or Bacteria- or Archaea-specific primers and were cloned. A total of 812 clones were screened by restriction fragment length polymorphisms (RFLP), approximately 50% of which were unique. All RFLP types that occurred more than once in the libraries, as well as many of the unique types, were sequenced. A total of 104 (94 bacterial and 10 archaeal) sequence types were determined. Of the 94 bacterial sequence types, 10 have no phylogenetic association with known taxonomic divisions and are phylogenetically grouped in six novel division level groups (candidate divisions WS1 to WS6); 21 belong to four recently described candidate divisions with no cultivated representatives (OPS, OP8, OP10, and OP11); and 63 are phylogenetically associated with 10 well-recognized divisions. The physiology of two particularly abundant sequence types obtained from the methanogenic zone could be inferred from their phylogenetic association with groups of microorganisms with a consistent phenotype. One of these sequence types is associated with the genus Syntrophus; Syntrophus spp. produce energy from the anaerobic oxidation of organic acids, with the production of acetate and hydrogen. The organism represented by the other sequence type is closely related to Methanosaeta spp., which are known to be capable of energy generation only through aceticlastic methanogenesis. We hypothesize, therefore, that the terminal step of hydrocarbon degradation in the methanogenic zone of the aquifer is aceticlastic methanogenesis and

  20. [Applicability of an electronic nose for detection of volatile chlorinated hydrocarbons in soil].

    PubMed

    Bu, Fan-Yang; Wen, Xiao-Gang; Wan, Mei; Liu, Rui; Cai, Qiang; Chen, Lü-Jun; Zhang, Yong-Ming

    2011-12-01

    An electronic nose principally composed of a photo ionization detector (PID) was developed for rapid detection of volatile chlorinated hydrocarbons (VCHs) in contaminated soil. Removal of interference gas such as benzene homologues with a pre-filtration tube was analyzed with gas chromatography (GC). A standard gas generator was applied to generate different concentrations of perchloroethylene (PCE) and trichloroethylene (TCE) gas, with which the determine precision and reproducibility of the electronic nose were evaluated by comparison with GC. Finally, simulated contamination soil with three typical paddy soils in Yangtze river delta region were used for ventilation purification experiments, the change of VCHs concentrations in the ventilation gas was monitored, based on which the applicability of the electronic nose was evaluated for on-line detection of the on-going of the ventilation purification process. Results showed that a halogenated hydrocarbon RAE-SEP tube was effective to remove interference gas, with 80%-97% of benzene homologues such as benzene and ethyl benzene being removed while more than 90% of VCHs passed through. With PCE or TCE gas, a linear dependence was derived between the data determined with the electronic nose and GC, the linear slope being 1.012 and R2 > 0.99. The electronic nose showed data consistent with GC (R2 > 0.99, n = 47) when applied for monitoring the remediation progress in a soil ventilation process. The electronic nose is therefore possibly applicable for rapid determination of soil pollution by VCHs, improving the efficiency of pollution diagnosis and remediation.

  1. Accuracy, precision, usability, and cost of free chlorine residual testing methods.

    PubMed

    Murray, Anna; Lantagne, Daniele

    2015-03-01

    Chlorine is the most widely used disinfectant worldwide, partially because residual protection is maintained after treatment. This residual is measured using colorimetric test kits varying in accuracy, precision, training required, and cost. Seven commercially available colorimeters, color wheel and test tube comparator kits, pool test kits, and test strips were evaluated for use in low-resource settings by: (1) measuring in quintuplicate 11 samples from 0.0-4.0 mg/L free chlorine residual in laboratory and natural light settings to determine accuracy and precision; (2) conducting volunteer testing where participants used and evaluated each test kit; and (3) comparing costs. Laboratory accuracy ranged from 5.1-40.5% measurement error, with colorimeters the most accurate and test strip methods the least. Variation between laboratory and natural light readings occurred with one test strip method. Volunteer participants found test strip methods easiest and color wheel methods most difficult, and were most confident in the colorimeter and least confident in test strip methods. Costs range from 3.50-444 USD for 100 tests. Application of a decision matrix found colorimeters and test tube comparator kits were most appropriate for use in low-resource settings; it is recommended users apply the decision matrix themselves, as the appropriate kit might vary by context.

  2. The Efficacy of Residual Chlorine Content on the Control of Legionella Spp. In Hospital Water Systems

    PubMed Central

    RAFIEE, Mohammad; MESDAGHINIA, Alireza; HAJJARAN, Homa; HAJAGHAZADEH, Mohammad; MIAHIPOUR, Abolfazl; JAHANGIRI-RAD, Mahsa

    2014-01-01

    Abstract Background Outbreaks of legionellosis may be a side effect of institution-water treatment. However, the long-term outcomes and the predictive factors of Legionella prevalence in such systems have still not been fully studied. This study was therefore conducted to investigate the prevalence of Legionella spp. and to evaluate the role of bacteriological water quality parameters on its prevalence and removal in hospital water systems. Methods A total of 45 samples were collected from distinct sites at seven hospitals in Tehran, Iran. The prevalence of this bacterium was assayed through a sensitive and specific technique for DNA detection using PCR. Multivariable stepwise regression analysis was used to explore the independent effects of the baseline factors on the incidence of Legionella. Two positive samples were also identified for species by DNA sequencing. Results Legionella were detected in 31.1% of samples. Showerheads and cold-water taps were the most and the least contaminated sources with 55.3 and 9 percent positive samples, respectively. Total mean of residual chlorine was 0.38 mg/L, with the peak value of 1.7 mg/L. Legionella detection was proportional to the residual chlorine content of water and the results indicated that residual chlorine content is a critical factor in the incidence and proliferation of Legionella (r=-0.33). The prevalence of Legionella also coincided with the prevalence of HPC and amoeba cysts. Conclusion The high positive rate of Legionella colonization shows that hospital-acquired legionellosis might be under diagnosed in studied hospitals. Further, Legionella colonization is independent of the type of water, system characteristics and of preventive maintenance measures. PMID:26060765

  3. Direct immunofluorescence and enzyme-linked immunosorbent assays for evaluating chlorinated hydrocarbon degrading bacteria

    SciTech Connect

    Brigmon, R.L.; Franck, M.M.; Brey, J.; Fliermans, C.B.; Scott, D.; Lanclos, K.

    1997-06-01

    Immunological procedures were developed to enumerate chlorinated hydrocarbon degrading bacteria. Polyclonal antibodies (Pabs) were produced by immunizing New Zealand white rabbits against 18 contaminant-degrading bacteria. These included methanotrophic and chlorobenzene (CB) degrading species. An enzyme-linked immunosorbent assay (ELISA) was used to test for specificity and sensitivity of the Pabs. Direct fluorescent antibodies (DFAs) were developed with these Pabs against select methanotrophic bacteria isolated from a trichloroethylene (TCE) contaminated landfill at the Savannah River Site (SRS) and cultures from the American Type Culture Collection (ATCC). Analysis of cross reactivity testing data showed some of the Pabs to be group specific while others were species specific. The threshold of sensitivity for the ELISA is 105 bacteria cells/ml. The DFA can detect as few as one bacterium per ml after concentration. Results from the DFA and ELISA techniques for enumeration of methanotrophic bacteria in groundwater were higher but not significantly different (P < 0.05) compared to indirect microbiological techniques such as MPN. These methods provide useful information on in situ community structure and function for bioremediation applications within 1--4 hours of sampling.

  4. Structural and dynamical properties of chlorinated hydrocarbons studied with resonant inelastic x-ray scattering

    NASA Astrophysics Data System (ADS)

    Bohinc, R.; Žitnik, M.; Bučar, K.; Kavčič, M.; Carniato, S.; Journel, L.; Guillemin, R.; Marchenko, T.; Kawerk, E.; Simon, M.; Cao, W.

    2016-04-01

    We present a theoretical and experimental study of resonant inelastic x-ray scattering on a large group of chlorinated hydrocarbons: CH3Cl, CH2Cl2, CHCl3, CCl4, CH3CH2Cl, ClCH2CH2Cl, CH3CHCl2, CH3CCl3, C2H2Cl2-iso, C2H2Cl2-cis, C2H2Cl2-trans, and C6H5Cl. Differences in structural and dynamical properties of the molecules generated by diverse chemical environments are observed in the measured Cl(Kα) spectral maps as well as in the Cl(K) total fluorescence yield spectra. The energy position, relative intensity, and the width of the Franck-Condon distribution of low-lying σ∗ and π∗ resonances are extracted by a fitting procedure taking into account the experimental broadening. The theoretical values obtained with the transition potential and Δ Kohn-Sham methods are in good agreement with the experimental parameters indicating subtle differences due to variations in the molecular structure.

  5. Contamination of stream fishes with chlorinated hydrocarbons from eggs of Great Lakes salmon

    SciTech Connect

    Merna, J.W.

    1986-01-01

    Pacific salmon Oncorhynchus spp. have been stocked in the Great Lakes where they accumulate body burdens of chlorinated hydrocarbons. The transport of these contaminants to resident communities in spawning streams was studied in two tributaries of Lake Michigan accessible to anadromous spawners and one control tributary blocked to them. No polychlorinated biphenyls (PCBs), DDT, or dieldrin were detected in the sediments or biota of the control stream, or in sediments of the test streams. However, trout Salmo spp. and, to a lesser extent, sculpins Cottus spp. accumulated PCBs and DDT as a result of eating contaminated salmon eggs. Eggs constituted as much as 87% (by weight) of the total stomach contents of trout collected during the salmon spawning season early October to early January. Salmon eggs contained 0.46-9.50 mg PCBs/kg,. and 0.14-1.80 mg DDT/kg. Consumption of eggs varied greatly among individual trout, and there was a strong correlation between numbers of eggs in the stomachs and PCB and DDT concentrations in the fillets.

  6. Microbiota associated with the migration and transformation of chlorinated aliphatic hydrocarbons in groundwater.

    PubMed

    Guan, Xiangyu; Liu, Fei; Xie, Yuxuan; Zhu, Lingling; Han, Bin

    2013-08-01

    Pollution of groundwater with chlorinated aliphatic hydrocarbons (CAHs) is a serious environmental problem which is threatening human health. Microorganisms are the major participants in degrading these contaminants. Here, groundwater contaminated for a decade with CAHs was investigated. Numerical simulation and field measurements were used to track and forecast the migration and transformation of the pollutants. The diversity, abundance, and possible activity of groundwater microbial communities at CAH-polluted sites were characterized by molecular approaches. The number of microorganisms was between 5.65E+05 and 1.49E+08 16S rRNA gene clone numbers per liter according to quantitative real-time PCR analysis. In 16S rRNA gene clone libraries constructed from samples along the groundwater flow, eight phyla were detected, and Proteobacteria were dominant (72.8 %). The microbial communities varied with the composition and concentration of pollutants. Meanwhile, toluene monooxygenases and methane monooxygenases capable of degradation of PCE and TCE were detected, demonstrating the major mechanism for PCE and TCE degradation and possibility for in situ remediation by addition of oxygen in this study.

  7. Isotopic and geochemical assessment of in situ biodegradation of chlorinated hydrocarbons.

    PubMed

    Kirtland, Brian C; Aelion, C Marjorie; Stone, Peter A; Hunkeler, Daniel

    2003-09-15

    Currently there is no in situ method to detect and quantify complete mineralization of chlorinated hydrocarbons (CHCs) to CO2. Combined isotopic measurements in conjunction with traditional chemical techniques were used to assess in situ biodegradation of trichloroethylene (TCE) and carbon tetrachloride (CT). Vadose zone CHC, ethene, ethane, methane, O2, and CO2 concentrations were analyzed using gas chromatography over 114 days at the Savannah River Site. delta13C of CHC and delta13C and 14C of vadose zone CO2, sediment organic matter, and groundwater dissolved inorganic carbon (DIC)were measured. Intermediate metabolites of TCE and CT accounted for < or = 10% of total CHCs. Delta13C of cis-1,2-dichloroethylene (DCE) was always heavier than TCE indicating substantial DCE biodegradation. 14C-CO2 values ranged from 84 to 128 percent modern carbon (pMC), suggesting that plant root-respired CO2 was dominant. 14C-CO2 values decreased over time (up to 12 pMC), and contaminated groundwater 14C-DIC (76 pMC) was substantially depleted relative to the control (121 pMC). 14C provided a direct measure of complete CHC mineralization in vadose zone and groundwater in situ and may improve remediation strategies.

  8. Determinants of the microbial community structure of eutrophic, hyporheic river sediments polluted with chlorinated aliphatic hydrocarbons.

    PubMed

    Hamonts, Kelly; Ryngaert, Annemie; Smidt, Hauke; Springael, Dirk; Dejonghe, Winnie

    2014-03-01

    Chlorinated aliphatic hydrocarbons (CAHs) often discharge into rivers as contaminated groundwater baseflow. As biotransformation of CAHs in the impacted river sediments might be an effective remediation strategy, we investigated the determinants of the microbial community structure of eutrophic, CAH-polluted sediments of the Zenne River. Based on PCR-DGGE analysis, a high diversity of Bacteria, sulfate-reducing bacteria, Geobacteraceae, methanogenic archaea, and CAH-respiring Dehalococcoides was found. Depth in the riverbed, organic carbon content, CAH content and texture of the sediment, pore water temperature and conductivity, and concentrations of toluene and methane significantly contributed to the variance in the microbial community structure. On a meter scale, CAH concentrations alone explained only 6% of the variance in the Dehalococcoides and sulfate-reducing communities. On a cm-scale, however, CAHs explained 14.5-35% of the variation in DGGE profiles of Geobacteraceae, methanogens, sulfate-reducing bacteria, and Bacteria, while organic carbon content explained 2-14%. Neither the presence of the CAH reductive dehalogenase genes tceA, bvcA, and vcrA, nor the community structure of the targeted groups significantly differed between riverbed locations showing either no attenuation or reductive dechlorination, indicating that the microbial community composition was not a limiting factor for biotransformation in the Zenne sediments.

  9. Numerical simulation of the thermal destruction of some chlorinated C sub 1 and C sub 2 hydrocarbons

    SciTech Connect

    Fisher, E.M.; Koshland, C.P. )

    1990-10-01

    The authors have numerically modeled the breakdown of small quantities of several chlorinated hydrocarbons (CH{sub 3}Cl, CH{sub 2}Cl{sub 2}, CHCl{sub 3}, CCl{sub 4}, C{sub 2}H{sub 3}Cl, and C{sub 2}H{sub 5}Cl) in a lean mixture of combustion products between 800 and 1,480 K. This simulates the fate of poorly atomized waste in a liquid-injection incinerator. Kinetics calculations were performed using the CHEMKIN and SENKIN programs, with a reaction mechanism that was developed at Louisiana State University to model flat-flame burner experiments. A 99.99-percent destruction efficiency was attained in one second at temperatures ranging from 1,280 to 960 k, with CCl{sub 4} requiring the highest temperature for destruction and C{sub 2}H{sub 5}Cl the lowest. For all compounds except C{sub 2}H{sub 5}Cl, there was a range of temperatures at which byproducts accounted for several percent of the elemental chlorine at the outlet. The more heavily chlorinated compounds formed more byproducts even though the amount of elemental chlorine was the same in all cases. The sensitivity of results to residence time, equivalence ratio, temperature profile, and the presence of additional chlorine, was examined for the case of CHCl{sub 3}.

  10. Reproductive and morphological condition of wild mink (Mustela vison) and river otters (Lutra canadensis) in relation to chlorinated hydrocarbon contamination.

    PubMed

    Harding, L E; Harris, M L; Stephen, C R; Elliott, J E

    1999-02-01

    We assessed chlorinated hydrocarbon contamination of mink and river otters on the Columbia and Fraser River systems of northwestern North America, in relation to morphological measures of condition. We obtained carcasses of mink and river otters from commercial trappers during the winters 1994-1995 and 1995-1996. Necropsies included evaluation of the following biological parameters: sex, body mass and length, age, thymus, heart, liver, lung, spleen, pancreas, kidney, gonad, omentum, adrenal gland and baculum masses, baculum length, and stomach contents. Livers were analyzed, individually or in pools, for residues of organochlorine (OC) pesticides, polychlorinated biphenyls (PCBs), dibenzo-p-dioxins, and dibenzofurans. Contaminant levels were relatively low compared to those documented in other North American populations, although they ranged higher than those detected during an earlier survey (1990-1992) of these regional populations. Body condition varied slightly among collection regions, but showed no relationship with contaminant burden. Mink from the upper Fraser River had less fat stores and also had some of the lowest OC contamination levels observed. Similarly, a few individuals with enlarged livers and kidneys had low contaminant levels. Although a few individual animals with gross abnormalities of reproductive systems did not show high levels of contamination, there was a significant negative correlation between total PCB concentrations (as Aroclor 1260) and baculum length in juvenile mink (r = 0.707; p = 0.033; n = 8). The association of juvenile baculum length with eventual reproductive success is unknown, but further characterization of reproductive organ morphology and relationship to contaminants should be undertaken in a larger subset of these populations. PMID:9924010

  11. Occurrence and profiles of chlorinated and brominated polycyclic aromatic hydrocarbons in waste incinerators.

    PubMed

    Horii, Yuichi; Ok, Gon; Ohura, Takeshi; Kannanct, Kurunthachalam

    2008-03-15

    Chlorinated polycyclic aromatic hydrocarbons (CIPAHs) have been reported to occur in urban air. Nevertheless, sources of CIPAHs in urban air have not been studied, due to the lack of appropriate analytical methods and standards. In this study, we measured concentrations of 20 CIPAHs and 11 brominated PAHs (BrPAHs) in fly ash and bottom ash from 11 municipal/hazardous/industrial waste incinerators, using analytical standards synthesized in our laboratory. Concentrations of total CIPAHs and BrPAHs in ash samples ranged from <0.06 to 6990 ng/g and from <0.14 to 1235 ng/g, respectively. The concentrations of CIPAHs were approximately 100-fold higher than the concentrations of BrPAHs. 6-CIBaP and 1-CIPyr were the dominant compounds in fly ash samples. The profiles of halogenated PAHs were similar to the profiles reported previously for urban air. 1-BrPyr was the predominant BrPAH in fly ash. Concentrations of 6-CIBaP, 9,10-Cl2Phe, 9-CIAnt, and 6-BrBaP in fly ash were significantly correlated with the corresponding parent PAH concentrations. Significant correlation between sigmaCIPAH and sigmaPAH concentrations suggests that direct chlorination of parent PAHs is the mechanism of formation of CIPAHs during incineration of wastes; nevertheless, a comparable correlation was not found for BrPAHs. There was no significant correlation between the capacity and temperature of an incinerator and the concentrations of sigmaCl-/BrPAHs in ash samples, although lower concentrations of all halogenated PAHs were found in stoker-type incinerators than in fixed grate-type incinerators. Toxicity equivalency quotients (TEQs) for CIPAHs in ash samples were calculated with CIPAH potencies. Average TEQ concentrations of CIPAHs in fly ash and bottom ash were15800 pg-TEQ/g and 67 pg-TEQ/g, respectively. Our results suggest that the extent of dioxin-like toxicity contributed by CIPAHs in ash generated during waste incineration is similar to that reported previously for dioxins. Waste

  12. Quantification of Degradation of Chlorinated Hydrocarbons in Saturated Low Permeability Sediments Using Compound-Specific Isotope Analysis.

    PubMed

    Wanner, Philipp; Parker, Beth L; Chapman, Steven W; Aravena, Ramon; Hunkeler, Daniel

    2016-06-01

    This field and modeling study aims to reveal if degradation of chlorinated hydrocarbons in low permeability sediments can be quantified using compound-specific isotope analysis (CSIA). For that purpose, the well-characterized Borden research site was selected, where an aquifer-aquitard system was artificially contaminated by a three component chlorinated solvent mixture (tetrachloroethene (PCE) 45 vol %, trichloroethene (TCE) 45 vol %, and chloroform (TCM) 10 vol %). Nearly 15 years after the contaminant release, several high-resolution concentration and CSIA profiles were determined for the chlorinated hydrocarbons that had diffused into the clayey aquitard. The CSIA profiles showed large shifts of carbon isotope ratios with depth (up to 24‰) suggesting that degradation occurs in the aquitard despite the small pore sizes. Simulated scenarios without or with uniform degradation failed to reproduce the isotope data, while a scenario with decreasing degradation with depth fit the data well. This suggests that nutrients had diffused into the aquitard favoring stronger degradation close to the aquifer-aquitard interface than with increasing depth. Moreover, the different simulation scenarios showed that CSIA profiles are more sensitive to different degradation conditions compared to concentration profiles highlighting the power of CSIA to constrain degradation activities in aquitards. PMID:27153381

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

    PubMed

    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.

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

    NASA Astrophysics Data System (ADS)

    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] ~ 1.9 mg L- 1, and initial aqueous [CAH] ~ 150 μg L- 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 ± 0.07 d- 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.

  15. Chlorinated hydrocarbon pesticides and polychlorinated biphenyls in sediment cores from San Francisco Bay

    USGS Publications Warehouse

    Venkatesan, M.I.; De Leon, R. P.; VanGeen, A.; Luoma, S.N.

    1999-01-01

    Sediment cores of known chronology from Richardson and San Pablo Bays in San Francisco Bay, CA, were analyzed for a suite of chlorinated hydrocarbon pesticides and polychlorinated biphenyls to reconstruct a historic record of inputs. Total DDTs (DDT = 2,4'- and 4,4'-dichlorodiphenyltrichloroethane and the metabolites, 2,4'- and 4,4'-DDE, -DDD) range in concentration from 4-21 ng/g and constitute a major fraction (> 84%) of the total pesticides in the top 70 cm of Richardson Bay sediment. A subsurface maximum corresponds to a peak deposition date of 1969-1974. The first measurable DDT levels are found in sediment deposited in the late 1930's. The higher DDT inventory in the San Pablo relative to the Richardson Bay core probably reflects the greater proximity of San Pablo Bay to agricultural activities in the watershed of the Sacramento and San Joaquin rivers. Total polychlorinated biphenyls (PCBs) occur at comparable levels in the two Bays (< 1-34 ng/g). PCBs are first detected in sediment deposited during the 1930's in Richardson Bay, about a decade earlier than the onset of detectable levels of DDTs. PCB inventories in San Pablo Bay are about a factor of four higher in the last four decades than in Richardson Bay, suggesting a distribution of inputs not as strongly weighed towards the upper reaches of the estuary as DDTs. The shallower subsurface maximum in PCBs compared to DDT in the San Pablo Bay core is consistent with the imposition of drastic source control measures four these constituents in 1970 and 1977 respectively. The observed decline in DDT and PCB levels towards the surface of both cores is consistent with a dramatic drop in the input of these pollutants once the effect of sediment resuspension and mixing is taken into account.

  16. Multifunctional iron-carbon nanocomposites through an aerosol-based process for the in situ remediation of chlorinated hydrocarbons.

    PubMed

    Zhan, Jingjing; Kolesnichenko, Igor; Sunkara, Bhanukiran; He, Jibao; McPherson, Gary L; Piringer, Gerhard; John, Vijay T

    2011-03-01

    Spherical iron-carbon nanocomposites were developed through a facile aerosol-based process with sucrose and iron chloride as starting materials. These composites exhibit multiple functionalities relevant to the in situ remediation of chlorinated hydrocarbons such as trichloroethylene (TCE). The distribution and immobilization of iron nanoparticles on the surface of carbon spheres prevents zerovalent nanoiron aggregation with maintenance of reactivity. The aerosol-based carbon microspheres allow adsorption of TCE, thus removing dissolved TCE rapidly and facilitating reaction by increasing the local concentration of TCE in the vicinity of iron nanoparticles. The strongly adsorptive property of the composites may also prevent release of any toxic chlorinated intermediate products. The composite particles are in the optimal range for transport through groundwater saturated sediments. Furthermore, those iron-carbon composites can be designed at low cost, the process is amenable to scale-up for in situ application, and the materials are intrinsically benign to the environment.

  17. Low-concentration tailing and subsequent quicklime-enhanced remediation of volatile chlorinated hydrocarbon-contaminated soils by mechanical soil aeration.

    PubMed

    Ma, Yan; Du, Xiaoming; Shi, Yi; Xu, Zhu; Fang, Jidun; Li, Zheng; Li, Fasheng

    2015-02-01

    Mechanical soil aeration has long been regarded as an effective ex-situ remediation technique and as suitable for remediation of large-scale sites contaminated by volatile organic compounds (VOCs) at low cost. However, it has been reported that the removal efficiency of VOCs from soil is relatively low in the late stages of remediation, in association with tailing. Tailing may extend the remediation time required; moreover, it typically results in the presence of contaminants residues at levels far exceeding regulations. In this context, the present study aimed to discuss the tailing that occurs during the process of remediation of soils contaminated artificially with volatile chlorinated hydrocarbons (VCHs) and to assess possible quicklime-enhanced removal mechanisms. The results revealed the following conclusions. First, temperature and aeration rate can be important controls on both the timing of appearance of tailing and the levels of residual contaminants. Furthermore, the addition of quicklime to soil during tailing can reduce the residual concentrations rapidly to below the remedial target values required for site remediation. Finally, mechanical soil aeration can be enhanced using quicklime, which can improve the volatilization of VCHs via increasing soil temperature, reducing soil moisture, and enhancing soil permeability. Our findings give a basic understanding to the elimination of the tailing in the application of mechanical soil aeration, particularly for VOCs-contaminated soils.

  18. Synergistic degradation of chlorinated hydrocarbons with microorganisms and zero valent iron

    NASA Astrophysics Data System (ADS)

    Schöftner, Philipp; Summer, Dorothea; Leitner, Simon; Watzinger, Andrea; Wimmer, Bernhard; Reichenauer, Thomas

    2016-04-01

    Sites contaminated with chlorinated hydrocarbons (CHC) are located mainly within build-up regions. Therefore in most cases only in-situ technologies without excavation of soil material can be used for remediation. This project examines a novel in-situ remediation method, in which the biotic degradation via bacteria is combined with abiotic degradation via zero-valent iron particles (ZVI). ZVI particles are injected into the aquifer where CHC-molecules are reductively dechlorinated. However Fe0 is also oxidized by reaction with water leading to generation of H2 without any CHC degradation. To achieve biotic degradation often strictly anaerobic strains of the bacteria Dehalococcoides are used. These bacteria can dechlorinate CHC by utilizing H2. By combining these processes the H2, produced during the anaerobic corrosion of Fe0, could be used by bacteria for further CHC degradation. Therefore the amount of used Fe0 and as a consequence also remediation costs could be reduced. Additionally the continuous supply of H2 could make the bacterial degradation more controllable. Different Fe0 particles (nano- and micro-scale) were tested for their perchloroethene (PCE) degradation rate and H2 production rate in microcosms. PCE-degradation rate by different bacterial cultures was investigated in the same microcosm system. In course of these experiments the 13C enrichment factors of the PCE degradation of the different particles and cultures were determined to enable the differentiation of biotic and abiotic degradation. Preliminary results showed, that the nano-scale particles reacted faster with PCE and water than their micro-scaled counterparts. The PCE degradation via micro-scaled particles lead to 13C enrichment factors in the range of -3,6 ‰ ± 0,6 to -9,5 ‰ ± 0,2. With one of the examined bacterial cultures a fast reduction of PCE to ethene was observed. Although PCE and TCE were completely degraded by this culture the metabolites DCE and VC could still be detected

  19. Patterns and trends of chlorinated hydrocarbons in nestling bald eagle (Haliaeetus leucocephalus) plasma in British Columbia and Southern California.

    PubMed

    Cesh, Lillian S; Williams, Tony D; Garcelon, David K; Elliott, John E

    2008-10-01

    Patterns and trends of chlorinated hydrocarbons were assessed in bald eagle nestling plasma from sites along the west coast of North America. Eagle plasma was sampled from four areas in southwestern British Columbia (BC), a reference site in northern BC, and from Santa Catalina Island, off the coast of California. Sites were chosen to reflect variation in contaminant exposure due to differing recent and/or historic anthropogenic activities. Santa Catalina Island had significantly greater mean concentrations of p,p'-DDE, 41.3 microg/kg wet weight (ww), than other sites, and Nanaimo/Crofton, BC had the greatest mean concentration of total PCBs, 28.9 microg/kg ww. Contaminant levels measured in 2003 in BC were compared to levels measured in 1993; over that ten year span, concentrations and patterns of chlorinated hydrocarbons have not significantly changed. There were no significant differences in levels of p,p'-DDE or hexachlorobenzene between 1993 and 2003, but significant decreases were found for trans-nonachlor and PCBs at BC sites. Levels of total PCBs and trans-nonachlor in the central Fraser Valley and Nanaimo/Crofton area have significantly decreased. Mean concentrations of p,p'-DDE measured in bald eagle nestling plasma samples in 2003 exceeded published criteria for effects on bald eagle reproduction at Santa Catalina Island and Barkley Sound, more than 30 years since heavy usage restrictions were imposed.

  20. Patterns and trends of chlorinated hydrocarbons in nestling bald eagle (Haliaeetus leucocephalus) plasma in British Columbia and Southern California.

    PubMed

    Cesh, Lillian S; Williams, Tony D; Garcelon, David K; Elliott, John E

    2008-10-01

    Patterns and trends of chlorinated hydrocarbons were assessed in bald eagle nestling plasma from sites along the west coast of North America. Eagle plasma was sampled from four areas in southwestern British Columbia (BC), a reference site in northern BC, and from Santa Catalina Island, off the coast of California. Sites were chosen to reflect variation in contaminant exposure due to differing recent and/or historic anthropogenic activities. Santa Catalina Island had significantly greater mean concentrations of p,p'-DDE, 41.3 microg/kg wet weight (ww), than other sites, and Nanaimo/Crofton, BC had the greatest mean concentration of total PCBs, 28.9 microg/kg ww. Contaminant levels measured in 2003 in BC were compared to levels measured in 1993; over that ten year span, concentrations and patterns of chlorinated hydrocarbons have not significantly changed. There were no significant differences in levels of p,p'-DDE or hexachlorobenzene between 1993 and 2003, but significant decreases were found for trans-nonachlor and PCBs at BC sites. Levels of total PCBs and trans-nonachlor in the central Fraser Valley and Nanaimo/Crofton area have significantly decreased. Mean concentrations of p,p'-DDE measured in bald eagle nestling plasma samples in 2003 exceeded published criteria for effects on bald eagle reproduction at Santa Catalina Island and Barkley Sound, more than 30 years since heavy usage restrictions were imposed. PMID:18253687

  1. Increased mortality odds ratio of male liver cancer in a community contaminated by chlorinated hydrocarbons in groundwater

    PubMed Central

    Lee, L; Chung, C; Ma, Y; Wang, G; Chen, P; Hwang, Y; Wang, J

    2003-01-01

    Aims: To investigate the association between cancer mortality risk and exposure to chlorinated hydrocarbons in groundwater of a downstream community near a contaminated site. Methods: Death certificates inclusive for the years 1966–97 were collected from two villages in the vicinity of an electronics factory operated between 1970 and 1992. These two villages were classified into the downstream (exposed) village and the upstream (unexposed) according to groundwater flow direction. Exposure classification was validated by the contaminant levels in 49 residential wells measured with gas chromatography/mass spectrometry. Mortality odds ratios (MORs) for cancer were calculated with cardiovascular-cerebrovascular diseases as the reference diseases. Multiple logistic regressions were performed to estimate the effects of exposure and period after adjustment for age. Results: Increased MORs were observed among males for all cancer, and liver cancer for the periods after 10 years of latency, namely, 1980–89, and 1990–97. Adjusted MOR for male liver cancer was 2.57 (95% confidence interval 1.21 to 5.46) with a significant linear trend for the period effect. Conclusion: The results suggest a link between exposure to chlorinated hydrocarbons and male liver cancer risk. However, the conclusion is limited by lack of individual information on groundwater exposure and potential confounding factors. PMID:12709523

  2. Evidence for Perchlorates and the Origin of Chlorinated Hydrocarbons Detected by SAM at the Rocknest Aeolian Deposit in Gale Crater

    NASA Technical Reports Server (NTRS)

    Glavin, Daniel P.; Freissinet, Caroline; Miller, Kristen E.; Eigenbrode, Jennifer L.; Brunner, Anna E.; Buch, Arnaud; Sutter, Brad; Archer, P. Douglas, Jr.; Atreya, Sushil K.; Brinckerhoff, William B.; Cabane, Michael; Coll, Patrice; Conrad, Pamela G.; Coscia, David; Dworkin, Jason P.; Franz, Heather B.; Grotzinger, John P.; Leshin, Laurie A.; Martin, Mildred G.; McKay, Christopher; Ming, Douglas W.; Navarro-Gonzalez, Rafael; Pavlov, Alexander; Steele, Andrew; Summons, Roger E.; Szopa, Cyril; Teinturier, Samuel; Mahaffy, Paul R.

    2013-01-01

    Four individual sample portions from a single scoop of the Rocknest aeolian deposit were sieved ( 150 m) and delivered to the Sample Analysis at Mars (SAM) instrument by the Mars Science Laboratory rover's sample acquisition system. The samples were analyzed separately by the SAM pyrolysis evolved gas and gas chromatography mass spectrometry analysis modes. Several chlorinated hydrocarbons including chloromethane, dichloromethane, trichloromethane, a chloromethylpropene, and chlorobenzene were identified by SAM above background levels with abundances of 0.01 to 2.3 nanomole.The evolution of the chloromethanes observed during pyrolysis is coincident with the increase in O2 released from the Rocknest sample and the decomposition of a product of N-methyl-N- (tert-butyldimethylsilyl)trifluoroacetamide (MTBSTFA), a chemical that leaked from a derivatization cup inside SAM.The best candidate for the oxychloride phase in Rocknest is a hydrated calcium perchlorate (Ca(ClO4)2nH2O), based on the temperature release of O2 that correlates with the release of the chlorinated species measured by SAM, although other chlorine bearing phases are being considered. Laboratory pyrolysis experiments suggest that reaction of martian chlorine with organic carbon from MTBSTFA can explain the presence of the chloromethanes and a chloromethylpropene also detected by SAM.However, we cannot exclude the possibility that traces of organic carbon of either martian or exogenous origin contributed to some of the chloromethanes measured by SAM. Although the alteration history and exposure age of the Rocknest deposit is unknown, it is possible that oxidative degradation of complex organic matter by ionizing radiation or other chemical processes in Rocknest has occurred.

  3. Interpreting residues of petroleum hydrocarbons in wildlife tissues

    USGS Publications Warehouse

    Hall, R.J.; Coon, N.C.

    1988-01-01

    A brief guidance publication that explains how to evaluate reports of petroleum concentrations in animal tissue. Sections on background, sampling and handling of samples, reports and interpretation, when to analyze for hydrocarbons, and how to interpret the magnitude of the concentrations.

  4. Biosurfactant-enhanced removal of residual hydrocarbon from soil

    NASA Astrophysics Data System (ADS)

    Bai, Guiyun; Brusseau, Mark L.; Miller, Raina M.

    1997-02-01

    An anionic monorhamnolipid biosurfactant produced by Pseudomonas aeruginosa was investigated for its potential to remove residual hexadecane from sand columns. In a series of column experiments, residual hexadecane saturation was established by pumping 14C-hexadecane into water-saturated sand columns and then flushing with water at a velocity of 25 cm h -1. Monorhamnolipid solutions of varying concentration were then applied to the columns at a velocity of 15 cm H -1 to remove the residual hexadecane. Of the rhamnolipid concentrations tested, which ranged from 40 to 1500 mg l -1, the optimal concentration for residual removal was 500 mg l -1, approximately ten times the critical micelle concentration (cmc). Approximately 84% of the residual was removed from the column packed with {20}/{30} mesh sand, and 22% was removed from the {40}/{50} mesh column. The primary mechanism for residual removal was mobilization (displacement and dispersion), whereas solubilization was found to be insignificant. The performance of monorhamnolipid was compared with that of two synthetic surfactant solutions on a mass basis (500 mg l -1) for the {40}/{50} mesh sand. Sodium dodecyl sulfate (0.2 X cmc), and polyoxyethylene (20) sorbitan monooleate (38 × cmc), removed 0% and 6.1% of the residual saturation, respectively.

  5. [Distribution of hydrocarbon residues in the sediment from Bizerte lagoon (Northern Tunisia)].

    PubMed

    Soussi, N

    1983-01-01

    The study of hydrocarbon residue by infrared spectrophotometry in the deposits of the Bizerta Lagoon allows us to recognize a polluted zone sector of the Menzel Bourguiba Arsenal. The Eastern part of the lagoon, a zone of "oyster parks" is not affected by pollution. Its average contents of hydrocarbon residues are clearly below the maximum content determined by international regulations. The distribution of hydrocarbon residues in the superficial sediments following three well differentiated zones, reflects the weak hydrodynamism in the lagoon. The vertical variations of this pollution agent contents show the preferential accumulation of the terrigenous material, from lake Ichkeul , in the western part and the weak rate of sedimentation in the eastern zone. PMID:6677195

  6. SIMULATION OF PERFORMANCE OF CHLORINE-FREE FLURORINATED ETHERS AND FLUORINATED HYDROCARBONS TO REPLACE CFC-11 AND CFC-114 IN CHILLERS

    EPA Science Inventory

    The paper discusses simulation of the performance of chlorine-free fluorinated ethers and fluorinated hydrocarbons as potential long-term replacements for CFC-11 and -114. Modeling has been done with in-house refrigeration models based on the Carnahan-Starling-DeSantis Equation o...

  7. Bidet toilet seats with warm-water tanks: residual chlorine, microbial community, and structural analyses.

    PubMed

    Iyo, Toru; Asakura, Keiko; Nakano, Makiko; Yamada, Mutsuko; Omae, Kazuyuki

    2016-02-01

    Despite the reported health-related advantages of the use of warm water in bidets, there are health-related disadvantages associated with the use of these toilet seats, and the bacterial research is sparse. We conducted a survey on the hygienic conditions of 127 warm-water bidet toilet seats in restrooms on a university campus. The spray water from the toilet seats had less residual chlorine than their tap water sources. However, the total viable microbial count was below the water-quality standard for tap water. In addition, the heat of the toilet seats' warm-water tanks caused heterotrophic bacteria in the source tap water to proliferate inside the nozzle pipes and the warm-water tanks. Escherichia coli was detected on the spray nozzles of about 5% of the toilet seats, indicating that the self-cleaning mechanism of the spray nozzles was largely functioning properly. However, Pseudomonas aeruginosa was detected on about 2% of the toilet seats. P. aeruginosa was found to remain for long durations in biofilms that formed inside warm-water tanks. Infection-prevention measures aimed at P. aeruginosa should receive full consideration when managing warm-water bidet toilet seats in hospitals in order to prevent opportunistic infections in intensive care units, hematology wards, and other hospital locations. PMID:26837831

  8. Bidet toilet seats with warm-water tanks: residual chlorine, microbial community, and structural analyses.

    PubMed

    Iyo, Toru; Asakura, Keiko; Nakano, Makiko; Yamada, Mutsuko; Omae, Kazuyuki

    2016-02-01

    Despite the reported health-related advantages of the use of warm water in bidets, there are health-related disadvantages associated with the use of these toilet seats, and the bacterial research is sparse. We conducted a survey on the hygienic conditions of 127 warm-water bidet toilet seats in restrooms on a university campus. The spray water from the toilet seats had less residual chlorine than their tap water sources. However, the total viable microbial count was below the water-quality standard for tap water. In addition, the heat of the toilet seats' warm-water tanks caused heterotrophic bacteria in the source tap water to proliferate inside the nozzle pipes and the warm-water tanks. Escherichia coli was detected on the spray nozzles of about 5% of the toilet seats, indicating that the self-cleaning mechanism of the spray nozzles was largely functioning properly. However, Pseudomonas aeruginosa was detected on about 2% of the toilet seats. P. aeruginosa was found to remain for long durations in biofilms that formed inside warm-water tanks. Infection-prevention measures aimed at P. aeruginosa should receive full consideration when managing warm-water bidet toilet seats in hospitals in order to prevent opportunistic infections in intensive care units, hematology wards, and other hospital locations.

  9. Effect of sediment contact and uptake mechanisms on accumulation of three chlorinated hydrocarbons in the midge, Chironomus riparius

    SciTech Connect

    Fry, D.M.; Fisher, S.W. )

    1990-05-01

    Chlorinated hydrocarbons (CHCs) are major contaminants of bottom sediments in many freshwater systems. The behavior and availability of sediment-sorbed compounds arouse much controversy due to the potential impact these contaminants could have on the ecosystem if they were to get into the food chain. Benthic organisms are at great risk from sediment-sorbed contaminants since they inhabit bottom sediments. In this investigation, uptake of sediment-sorbed 5,5{prime},6-trichlorobiphenyl (PCB), p,p{prime}-DDE and PCP by the midge (Chironomus riparius) was examined under 3 conditions. Uptake from direct contact with contaminated sediment (sediment + water) was compared to uptake levels by the midge when it was screened from contaminated sediment contact (screened sediment) and to uptake in dead organisms exposed to contaminated sediment (passive).

  10. Polynuclear aromatic and chlorinated hydrocarbons in mussels from the coastal zone of Ushuaia, Tierra del Fuego, Argentina.

    PubMed

    Amin, Oscar A; Comoglio, Laura I; Sericano, José L

    2011-03-01

    Mussels (Mytilus edulis chilensis) were collected from 12 coastal locations in Ushuaia Bay, Argentina, and the surrounding area in October 1999 and again in October 2003. Concentrations of polynuclear aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), and selected chlorinated pesticides were determined to assess the impact of a fast-growing population in the area. Total PAH concentrations ranged from 2.24 to an extremely high concentration of 2,420 µg/g lipid measured in mussels collected near an oil jetty used to discharge to shore storage tanks. The composition of PAHs in these samples indicates that the source of these compounds inside Ushuaia Bay is predominantly petrogenic, with some pyrogenic background, whereas mostly pyrogenic-related PAHs were evident in areas outside the bay. Total concentrations of PCBs ranged between 12.8 and 8,210 ng/g lipid, with the highest concentration, detected inside Ushuaia harbor, representing a 10-fold increase when compared with historical data. Chlorinated pesticides were detected at comparatively lower concentrations, with 4-4'- 1,1-dichloro-2,2-bis(p-chlorophenyl)ethylene being the most common. The aggressive increase in population and related activities observed in the city of Ushuaia over the last two decades might have affected the environmental quality of the local bay. Moreover, the oceanographic and atmospheric conditions existing in Ushuaia Bay and surrounding areas may favor the accumulation and long-term presence of these organic pollutants in all compartments of this fragile environment.

  11. Polycyclic aromatic hydrocarbons residues in sandstorm depositions in Beijing, China.

    PubMed

    Fu, S; Li, K; Xia, X J; Xu, X B

    2009-02-01

    This study was conducted to determine the concentration of 16 polycyclic aromatic hydrocarbons (PAHs) in sandstorm depositions in Beijing, China. The PAH concentrations in 13 samples collected in Beijing ranged from 0.18 to 3.52 microg g(-1). Analysis of the sources of contamination revealed that the PAHs were derived from a coal combustion source, although various effects of traffic emissions were also observed. Furthermore, the PAH levels in Beijing tended to be higher in the southeast. Finally, the nemerow composite index revealed that the degree of pollution in the sandstorm depositions varied widely among sampling sites.

  12. Polycyclic aromatic hydrocarbons residues in sandstorm depositions in Beijing, China

    SciTech Connect

    Fu, S.; Li, K.; Xia, X.J.; Xu, X.B.

    2009-02-15

    This study was conducted to determine the concentration of 16 polycyclic aromatic hydrocarbons (PAHs) in sandstorm depositions in Beijing, China. The PAH concentrations in 13 samples collected in Beijing ranged from 0.18 to 3.52 {mu} g g{sup -1}. Analysis of the sources of contamination revealed that the PAHs were derived from a coal combustion source, although various effects of traffic emissions were also observed. Furthermore, the PAH levels in Beijing tended to be higher in the southeast. Finally, the Nemerow composite index revealed that the degree of pollution in the sandstorm depositions varied widely among sampling sites.

  13. Polycyclic aromatic hydrocarbons residues in sandstorm depositions in Beijing, China.

    PubMed

    Fu, S; Li, K; Xia, X J; Xu, X B

    2009-02-01

    This study was conducted to determine the concentration of 16 polycyclic aromatic hydrocarbons (PAHs) in sandstorm depositions in Beijing, China. The PAH concentrations in 13 samples collected in Beijing ranged from 0.18 to 3.52 microg g(-1). Analysis of the sources of contamination revealed that the PAHs were derived from a coal combustion source, although various effects of traffic emissions were also observed. Furthermore, the PAH levels in Beijing tended to be higher in the southeast. Finally, the nemerow composite index revealed that the degree of pollution in the sandstorm depositions varied widely among sampling sites. PMID:18773130

  14. 40 CFR 180.526 - Synthetic isoparaffinic petroleum hydrocarbons; tolerances for residues.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... residues. (a) General. Synthetic isoparaffinic petroleum hydrocarbons complying with 21 CFR 172.882 (a) and... 40 CFR part 180 and in this part. (b) Section 18 emergency exemptions. (c) Tolerances with regional... 40 Protection of Environment 25 2012-07-01 2012-07-01 false Synthetic isoparaffinic...

  15. 40 CFR 180.526 - Synthetic isoparaffinic petroleum hydrocarbons; tolerances for residues.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... residues. (a) General. Synthetic isoparaffinic petroleum hydrocarbons complying with 21 CFR 172.882 (a) and... 40 CFR part 180 and in this part. (b) Section 18 emergency exemptions. (c) Tolerances with regional... 40 Protection of Environment 23 2010-07-01 2010-07-01 false Synthetic isoparaffinic...

  16. 40 CFR 180.526 - Synthetic isoparaffinic petroleum hydrocarbons; tolerances for residues.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... residues. (a) General. Synthetic isoparaffinic petroleum hydrocarbons complying with 21 CFR 172.882 (a) and... 40 CFR part 180 and in this part. (b) Section 18 emergency exemptions. (c) Tolerances with regional... 40 Protection of Environment 25 2013-07-01 2013-07-01 false Synthetic isoparaffinic...

  17. 40 CFR 180.526 - Synthetic isoparaffinic petroleum hydrocarbons; tolerances for residues.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... residues. (a) General. Synthetic isoparaffinic petroleum hydrocarbons complying with 21 CFR 172.882 (a) and... 40 CFR part 180 and in this part. (b) Section 18 emergency exemptions. (c) Tolerances with regional... 40 Protection of Environment 24 2011-07-01 2011-07-01 false Synthetic isoparaffinic...

  18. 40 CFR 180.526 - Synthetic isoparaffinic petroleum hydrocarbons; tolerances for residues.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... residues. (a) General. Synthetic isoparaffinic petroleum hydrocarbons complying with 21 CFR 172.882 (a) and... 40 CFR part 180 and in this part. (b) Section 18 emergency exemptions. (c) Tolerances with regional... 40 Protection of Environment 24 2014-07-01 2014-07-01 false Synthetic isoparaffinic...

  19. TAILORING CATALYSTS FOR HYDRODECHLORINATING CHLORINATED HYDROCARBON CONTAMINANTS IN GROUNDWATER. (R825689C093)

    EPA Science Inventory

    Abstract

    A palladium-on-zeolite catalyst has been optimized for treating groundwater contaminated with halogenated hydrocarbon compounds (HHCs) by hydrodechlorination with dissolved hydrogen. Aqueous sulfite was used as the model poison and the dechlorination of 1,2-di...

  20. TAILORING CATALYSTS FOR HYDRODECHLORINATING CHLORINATED HYDROCARBON CONTAMINANTS IN GROUNDWATER. (R825689C078)

    EPA Science Inventory

    Abstract

    A palladium-on-zeolite catalyst has been optimized for treating groundwater contaminated with halogenated hydrocarbon compounds (HHCs) by hydrodechlorination with dissolved hydrogen. Aqueous sulfite was used as the model poison and the dechlorination of 1,2-di...

  1. BIOTRANSFORMATION OF MONOAROMATIC AND CHLORINATED HYDROCARBONS AT AN AVIATION GASOLINE SPILL SITE

    EPA Science Inventory

    A shallow water table aquifer under the U.S. Coast Guard Air Station at Traverse City, MI, has acclimated to the aerobic and anaerobic transformation of monoaromatic hydrocarbons (BTX) released from an aviation gasoline spill. The aquifer also exhibits reductive dechlorination of...

  2. Chlorinated hydrocarbons in the marine environment. A report prepared by the Panel on Monitoring Persistent Pesticides in the Marine Environment of the Committee on Oceanography

    USGS Publications Warehouse

    ,; Goldberg, E.D.; Butler, P.; Meier, P.; Menzel, D.; Paulik, G.; Risebrough, R.; Stickel, L.F.

    1971-01-01

    SUMMARY AND RECOMMENDATIONS : The oceans are an ultimate accumulation site for the persistent chlorinated hydrocarbons. As much as 25 percent of the DDT compounds produced to date may have been transferred to the sea. The amount of DDT compounds in the marine biota is estimated to be less than 0.1 percent of total production, yet this amount has produced a demonstrable impact upon the marine environment. Populations of fish-eating birds have experienced reproductive failure and decline. With continued accumulations of persistent chlorinated hydrocarbons in the marine ecosystem, additional species will be threatened. Continued release of these pollutants to the environment can only accelerate the accumulation of unacceptable levels of persistent chlorinated hydrocarbons in the tissues of marine food fish. Certain risks in the utilization of chlorinated hydrocarbons are especially hard to quantify, but they require serious consideration. The rate at which such substances degrade to harmless products in the marine system is unknown; the half-lives of some of the more persistent materials are certainly of the order of years, and perhaps even of decades or centuries. If most of the remaining 75 percent of the persistent chlorinated hydrocarbons is now in reservoirs that will in time transfer their contents to the sea, we may expect an increased level of these substances in marine organisms, despite future improvements of manufacturing practices. In fact, if these compounds degrade with half-lives of decades or longer, there will be no opportunity to redress the consequences. The more the problems are studied, the more unexpected effects are identified. In view of the findings of the past decade, our prediction of the potential hazards of chlorinated hydrocarbons in the marine environment may be vastly underestimated. The Panel makes the following recommendations, which will be developed and expanded in the remainder of the report: ? A massive national effort should be

  3. Natural attenuation of chlorinated-hydrocarbon contamination at Fort Wainwright, Alaska; a hydrogeochemical and microbiological investigation workplan

    USGS Publications Warehouse

    McCarthy, Kathleen A.; Lilly, Michael R.; Braddock, Joan F.; Hinzman, Larry D.

    1998-01-01

    Natural attenuation processes include biological degradation, by which microorganisms break down contaminants into simpler product compounds; adsorption of contaminants to soil particles, which decreases the mass of contaminants dissolved in ground water; and dispersion, which decreases dissolved contaminant concentrations through dilution. The primary objectives of this study are to (1) assess the degree to which such natural processes are attenuating chlorinated-hydrocarbon contamination in ground water, and (2) evaluate the effects of ground-water/surface-water interactions on natural-attenuation processes in the area of the former East and West Quartermasters Fueling Systems for Fort Wainwright, Alaska. The study will include investigations of the hydrologic, geochemical, and microbiological processes occurring at this site that influence the transport and fate of chlorinated hydrocarbons in ground water. To accomplish these objectives, a data-collection program has been initiated that includes measurements of water-table elevations and the stage of the Chena River; measurements of vertical temperature profiles within the subsurface; characterization of moisture distribution and movement in the unsaturated zone; collection of ground-water samples for determination of both organic and inorganic chemical constituents; and collection of ground-water samples for enumeration of microorganisms and determination of their potential to mineralize contaminants. We will use results from the data-collection program described above to refine our conceptual model of hydrology and contaminant attenuation at this site. Measurements of water-table elevations and river stage will help us to understand the magnitude and direction of ground-water flow and how changes in the stage of the Chena River affect ground-water flow. Because ambient ground water and surface water typically have different temperature characteristics, temperature monitoring will likely provide further insight

  4. Polychlorinated naphthalenes and other chlorinated tricyclic aromatic hydrocarbons emitted from combustion of polyvinylchloride.

    PubMed

    Wang, Dongli; Xu, Xiaobai; Chu, Shaogang; Li, Qing X

    2006-11-16

    Chloronaphthalenes (CNs) and phenanthrenes or/and anthracenes (CP/CAs) were detected in the emissions of polyvinylchloride (PVC) combustion at 900 degrees C. The presence of metallic iron, copper, or aluminum increased the formation of highly chlorinated CNs (tri- to octachloro-homologues) in the PVC combustion process. Total levels of CNs and CP/CAs were 40-48 and 76-116 mg/kg PVC, respectively, in the emissions from combustion of PVC with metals. Monochloronaphthalenes, dichloronaphtahlenes, monochlorophenanthrenes, and monochloroanthracenes were the predominant homologues. The other CN homologues were minor combustion byproducts. Detection of CNs in the PVC combustion emissions suggests that CN formation from solid waste incineration is a source of CNs in the environment. PMID:16982140

  5. In situ recovery from residually heated sections in a hydrocarbon containing formation

    SciTech Connect

    Vinegar, Harold J.; Karanikas, John Michael; Ryan, Robert Charles

    2010-12-14

    Methods of treating a tar sands formation is described herein. The methods may include providing heat to a first section of a hydrocarbon layer in the formation from a plurality of heaters located in the first section of the formation. Heat is transferred from the heaters so that at least a first section of the formation reaches a selected temperature. At least a portion of residual heat from the first section transfers from the first section to a second section of the formation. At least a portion of hydrocarbons in the second section are mobilized by providing a solvation fluid and/or a pressurizing fluid to the second section of the formation.

  6. Structures and Nuclear Quadrupole Coupling Tensors of a Series of Chlorine-Containing Hydrocarbons

    NASA Astrophysics Data System (ADS)

    Dikkumbura, Asela S.; Webster, Erica R.; Dorris, Rachel E.; Peebles, Rebecca A.; Peebles, Sean A.; Seifert, Nathan A.; Pate, Brooks

    2016-06-01

    Rotational spectra for gauche-1,2-dichloroethane (12DCE), gauche-1-chloro-2-fluoroethane (1C2FE) and both anti- and gauche-2,3-dichloropropene (23DCP) have been observed using chirped-pulse Fourier-transform microwave (FTMW) spectroscopy in the 6-18 GHz region. Although the anti conformers for all three species are predicted to be more stable than the gauche forms, they are nonpolar (12DCE) or nearly nonpolar (predicted dipole components for anti-1C2FE: μ_a = 0.11 D, μ_b = 0.02 D and for anti-23DCP: μ_a = 0.25 D, μ_b = 0.02 D); nevertheless, it was also possible to observe and assign the spectrum of anti-23DCP. Assignments of parent spectra and 37Cl and 13C substituted isotopologues utilized predictions at the MP2/6-311++G(2d,2p) level and Pickett's SPCAT/SPFIT programs. For the weak anti-23DCP spectra, additional measurements also utilized a resonant-cavity FTMW spectrometer. Full chlorine nuclear quadrupole coupling tensors for gauche-12DCE and both anti- and gauche-23DCP have been diagonalized to allow comparison of coupling constants. Kraitchman's equations were used to determine r_s coordinates of isotopically substituted atoms and r_0 structures were also deduced for gauche conformers of 12DCE and 1C2FE. Structural details and chlorine nuclear quadrupole coupling constants of all three molecules will be compared, and effects of differing halogen substitution and carbon chain length on molecular properties will be evaluated.

  7. Polycyclic aromatic hydrocarbons, polychlorinated biphenyls, and chlorinated pesticides in background air in central Europe - investigating parameters affecting wet scavenging of polycyclic aromatic hydrocarbons

    NASA Astrophysics Data System (ADS)

    Shahpoury, P.; Lammel, G.; Holubová Šmejkalová, A.; Klánová, J.; Přibylová, P.; Váňa, M.

    2014-10-01

    Concentrations of polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), and chlorinated pesticides (CPs) were measured in air and precipitation at a background site in central Europe. Σ PAH concentrations in air and rainwater ranged from 0.7 to 327.9 ng m-3 and below analytical method detection limit (< MDL) to 2.1 × 103 ng L-1. The concentrations of PCBs and CPs in rainwater were < MDL. Σ PCB and Σ CP concentrations in air ranged from < MDL to 44.6 and < MDL to 351.7 pg m-3, respectively. The potential relationships between PAH wet scavenging and particulate matter and rainwater properties were investigated. The concentrations of ionic species in particulate matter and rainwater were significantly correlated, highlighting the importance of particle scavenging process. Overall, higher scavenging efficiencies were found for relatively less volatile PAHs, underlining the effect of analyte gas-particle partitioning on scavenging process. The PAH wet scavenging was more effective when the concentrations of ionic species were high. In addition, the elemental and organic carbon contents of the particulate matter were found to influence the PAH scavenging.

  8. Polycyclic aromatic hydrocarbons, polychlorinated biphenyls, and chlorinated pesticides in background air in central Europe - investigating parameters affecting wet scavenging of polycyclic aromatic hydrocarbons

    NASA Astrophysics Data System (ADS)

    Shahpoury, P.; Lammel, G.; Holubová Šmejkalová, A.; Klánová, J.; Přibylová, P.; Váňa, M.

    2015-02-01

    Concentrations of polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), and chlorinated pesticides (CPs) were measured in air and precipitation at a background site in central Europe. ∑ PAH concentrations in air and rainwater ranged from 0.7 to 327.9 ng m-3 and below limit of quantification (< LOQ) to 2.1 × 103 ng L-1. The concentrations of PCBs and CPs in rainwater were < LOQ. ∑ PCB and ∑ CP concentrations in air ranged from < LOQ to 44.6 and < LOQ to 351.7 pg m-3, respectively. The potential relationships between PAH wet scavenging and particulate matter and rainwater properties were investigated. The concentrations of ionic species in particulate matter and rainwater were significantly correlated, highlighting the importance of particle scavenging process. Overall, higher scavenging efficiencies were found for relatively less volatile PAHs, underlining the effect of analyte gas-particle partitioning on scavenging process. The particulate matter removal by rain, and consequently PAH wet scavenging, was more effective when the concentrations of ionic species were high. In addition, the elemental and organic carbon contents of the particulate matter were found to influence the PAH scavenging.

  9. Temporal variations in natural attenuation of chlorinated aliphatic hydrocarbons in eutrophic river sediments impacted by a contaminated groundwater plume.

    PubMed

    Hamonts, Kelly; Kuhn, Thomas; Vos, Johan; Maesen, Miranda; Kalka, Harald; Smidt, Hauke; Springael, Dirk; Meckenstock, Rainer U; Dejonghe, Winnie

    2012-04-15

    Chlorinated aliphatic hydrocarbons (CAHs) often discharge into rivers as contaminated groundwater baseflow. Biotransformation, sorption and dilution of CAHs in the impacted river sediments have been reported to reduce discharge, but the effect of temporal variations in environmental conditions on the occurrence and extent of those processes in river sediments is largely unknown. We monitored the reduction of CAH discharge into the Zenne River during a 21-month period. Despite a relatively stable influx of CAHs from the groundwater, the total reduction in CAH discharge from 120 to 20 cm depth in the river sediments, on average 74 ± 21%, showed moderate to large temporal variations, depending on the riverbed location. High organic carbon and anaerobic conditions in the river sediments allowed microbial reductive dechlorination of both chlorinated ethenes and chlorinated ethanes. δ(13)C values of the CAHs showed that this biotransformation was remarkably stable over time, despite fluctuating pore water temperatures. Daughter products of the CAHs, however, were not detected in stoichiometric amounts and suggested the co-occurrence of a physical process reducing the concentrations of CAHs in the riverbed. This process was the main process causing temporal variations in natural attenuation of the CAHs and was most likely dilution by surface water-mixing. However, higher spatial resolution monitoring of flow transients in the riverbed is required to prove dilution contributions due to dynamic surface water-groundwater flow exchanges. δ(13)C values and a site-specific isotope enrichment factor for reductive dechlorination of the main groundwater pollutant vinyl chloride (VC) allowed assessment of changes over time in the extent of both biotransformation and dilution of VC for different scenarios in which those processes either occurred consecutively or simultaneously between 120 and 20 cm depth in the riverbed. The extent of reductive dechlorination of VC ranged from 27

  10. Simulation of ground-water flow and transport of chlorinated hydrocarbons at Graces Quarters, Aberdeen Proving Ground, Maryland

    USGS Publications Warehouse

    Tenbus, Frederick J.; Fleck, William B.

    2001-01-01

    Military activity at Graces Quarters, a former open-air chemical-agent facility at Aberdeen Proving Ground, Maryland, has resulted in ground-water contamination by chlorinated hydrocarbons. As part of a ground-water remediation feasibility study, a three-dimensional model was constructed to simulate transport of four chlorinated hydrocarbons (1,1,2,2-tetrachloroethane, trichloroethene, carbon tetrachloride, and chloroform) that are components of a contaminant plume in the surficial and middle aquifers underlying the east-central part of Graces Quarters. The model was calibrated to steady-state hydraulic head at 58 observation wells and to the concentration of 1,1,2,2-tetrachloroethane in 58 observation wells and 101direct-push probe samples from the mid-1990s. Simulations using the same basic model with minor adjustments were then run for each of the other plume constituents. The error statistics between the simulated and measured concentrations of each of the constituents compared favorably to the error statisticst,1,2,2-tetrachloroethane calibration. Model simulations were used in conjunction with contaminant concentration data to examine the sources and degradation of the plume constituents. It was determined from this that mixed contaminant sources with no ambient degradation was the best approach for simulating multi-species solute transport at the site. Forward simulations were run to show potential solute transport 30 years and 100 years into the future with and without source removal. Although forward simulations are subject to uncertainty, they can be useful for illustrating various aspects of the conceptual model and its implementation. The forward simulation with no source removal indicates that contaminants would spread throughout various parts of the surficial and middle aquifers, with the100-year simulation showing potential discharge areas in either the marshes at the end of the Graces Quarters peninsula or just offshore in the estuaries. The

  11. Health risk assessment on residents exposed to chlorinated hydrocarbons contaminated in groundwater of a hazardous waste site.

    PubMed

    Lee, Lukas Jyuhn-hsiarn; Chan, Chang-Chuan; Chung, Chih-Wen; Ma, Yee-Chung; Wang, Gan-Shuh; Wang, Jung-Der

    2002-02-01

    We conducted this study to estimate residents' chronic hazard and carcinogenic risk in a groundwater-contaminated community after on-site remediation in Taiwan during 1999-2000. We followed guidelines for assessing hazardous waste sites of the U.S. Environmental Protection Agency (EPA) and used empirically measured contaminant levels and exposure parameters to perform health risk assessment on seven chlorinated hydrocarbons. We measured groundwater concentrations of vinyl chloride, tetrachloroethylene, trichloroethylene, 1,1-dichloroethylene, 1,1,1-trichloroethane, cis-1,2-dichloroethylene, and 1,1-dichloroethane in 49 off-site residential wells by gas chromatography/mass spectrometry. Exposure parameters were mainly derived from our field survey of 382 residents, and partially from U.S. EPA default values. Total exposure dose estimation included routes of inhalation during showering and dermal absorption of showers and other activities involved with hand-water contacts. The ingestion route of water was not included because most residents drank boiled water with negligible contaminants. We calculated a hazard index (HI) for all seven chlorinated hydrocarbons and carcinogenic risks for known human carcinogen of vinyl chloride and probable human carcinogens of tetrachloroethylene and trichloroethylene, which had the same target organ, the liver. The HI values for reasonable maximal exposure (RME) and average exposure were 14.3 and 0.2, respectively. The cancer risks based on RME and average exposure (in parentheses) for vinyl chloride, tetrachloroethylene, and trichloroethylene were 8.4 x 10(-6) (7.3 x 10(-9)), 1.9 x 10(-4) (1.3 x 10(-7)), and 1.4 x 10(-4) (1.2 x 10(-6)), respectively. We applied Monte Carlo simulations to the sensitivity analysis, which showed that the contaminant levels, exposure duration, and time for showers were major determinants of health risks. We concluded that the contaminated groundwater was still unsafe for use even after the contaminated

  12. Evaluation of Membrane Ultrafiltration and Residual Chlorination as a Decentralized Water Treatment Strategy for Ten Rural Healthcare Facilities in Rwanda

    PubMed Central

    Huttinger, Alexandra; Dreibelbis, Robert; Roha, Kristin; Ngabo, Fidel; Kayigamba, Felix; Mfura, Leodomir; Moe, Christine

    2015-01-01

    There is a critical need for safe water in healthcare facilities (HCF) in low-income countries. HCF rely on water supplies that may require additional on-site treatment, and need sustainable technologies that can deliver sufficient quantities of water. Water treatment systems (WTS) that utilize ultrafiltration membranes for water treatment can be a useful technology in low-income countries, but studies have not systematically examined the feasibility of this technology in low-income settings. We monitored 22 months of operation of 10 WTS, including pre-filtration, membrane ultrafiltration, and chlorine residual disinfection that were donated to and operated by rural HCF in Rwanda. The systems were fully operational for 74% of the observation period. The most frequent reasons for interruption were water shortage (8%) and failure of the chlorination mechanism (7%). When systems were operational, 98% of water samples collected from the HCF taps met World Health Organization (WHO) guidelines for microbiological water quality. Water quality deteriorated during treatment interruptions and when water was stored in containers. Sustained performance of the systems depended primarily on organizational factors: the ability of the HCF technician to perform routine servicing and repairs, and environmental factors: water and power availability and procurement of materials, including chlorine and replacement parts in Rwanda. PMID:26516883

  13. Evaluation of Membrane Ultrafiltration and Residual Chlorination as a Decentralized Water Treatment Strategy for Ten Rural Healthcare Facilities in Rwanda.

    PubMed

    Huttinger, Alexandra; Dreibelbis, Robert; Roha, Kristin; Ngabo, Fidel; Kayigamba, Felix; Mfura, Leodomir; Moe, Christine

    2015-10-01

    There is a critical need for safe water in healthcare facilities (HCF) in low-income countries. HCF rely on water supplies that may require additional on-site treatment, and need sustainable technologies that can deliver sufficient quantities of water. Water treatment systems (WTS) that utilize ultrafiltration membranes for water treatment can be a useful technology in low-income countries, but studies have not systematically examined the feasibility of this technology in low-income settings. We monitored 22 months of operation of 10 WTS, including pre-filtration, membrane ultrafiltration, and chlorine residual disinfection that were donated to and operated by rural HCF in Rwanda. The systems were fully operational for 74% of the observation period. The most frequent reasons for interruption were water shortage (8%) and failure of the chlorination mechanism (7%). When systems were operational, 98% of water samples collected from the HCF taps met World Health Organization (WHO) guidelines for microbiological water quality. Water quality deteriorated during treatment interruptions and when water was stored in containers. Sustained performance of the systems depended primarily on organizational factors: the ability of the HCF technician to perform routine servicing and repairs, and environmental factors: water and power availability and procurement of materials, including chlorine and replacement parts in Rwanda. PMID:26516883

  14. Chlorinated hydrocarbons in early life stages of the common snapping turtle (Chelydra serpentina serpentina) from a coastal wetland on Lake Ontario, Canada

    SciTech Connect

    Bishop, C.A.; Lean, D.R.S.; Carey, J.H.; Brooks, R.J.; Ng, P.

    1995-03-01

    To assess intra-clutch variation in contaminant concentrations in eggs, and to investigate the dynamics of chlorinated hydrocarbon accumulation in embryos of the common snapping turtle (Chelydra serpentina), concentrations of p,p{prime}-DDE, hexachlorobenzene, trans-nonachlor, cis-chlordane, and six PCB congeners were measured in eggs, embryos, and hatchlings. Samples were collected from Cootes Paradise, a wetland at the western end of Lake Ontario, Ontario, Canada. The intra-clutch variation in chlorinated hydrocarbon concentrations within four snapping turtle clutches was determined by analyzing the first, last, and middle five eggs oviposited in the nest. The first five eggs had the highest mean concentrations of all chlorinated hydrocarbons, wet weight, and egg diameter. On a lipid weight basis, the first five eggs contained the highest concentration of all compounds except total PCBs and cis-chlordane. The concentration of cis-chlordane was the only parameter measured that was significantly different among the three sets of eggs. At hatching, snapping turtles without yolk sacs contained from 55.2 to 90.5% of the absolute amount of organochlorine compounds measured in the egg at oviposition. Eighteen days after hatching, the body burden of PCBs and pesticides decreased to 45.3 to 62.2% of that in the fresh egg. The accumulation of organochlorine chemicals in embryonic turtles peaked at or just before hatching and then declined thereafter, which is consistent with trends reported in developing sea turtles, fish, and birds.

  15. Secondary aerosol formation from the oxidation of biogenic hydrocarbons by chlorine atoms

    NASA Astrophysics Data System (ADS)

    Cai, Xuyi; Griffin, Robert J.

    2006-07-01

    The chlorine atom (Cl) is a potential oxidant of volatile organic compounds (VOCs) in the atmosphere and is hypothesized to lead to secondary organic aerosol (SOA) formation in coastal and industrialized areas. The purpose of this paper is to test this hypothesis and to quantify the SOA formation potentials of the common monoterpenes α-pinene, β-pinene, and d-limonene when oxidized by Cl in laboratory chamber experiments. Results indicate that the oxidation of these monoterpenes generates significant amounts of aerosol. The SOA yields of α-pinene, β-pinene, and d-limonene in this study are comparable to those when they are oxidized by ozone, by nitrate radical, and in photooxidation scenarios. For aerosol mass up to 30.0 μg m-3, their yields reach approximately 0.20, 0.20, and 0.30, respectively. For d-limonene, data indicate two yield curves that depend on the initial concentration ratio of Cl precursor to d-limonene. It is argued theoretically that multiple SOA yield curves may be common for VOCs, depending on the initial concentration ratio of oxidant to VOC. SOA formation from the three typical monoterpenes when oxidized by Cl in the marine boundary layer, coastal areas, and inland industrialized areas could be a source of organic aerosol in the early morning.

  16. Modelling of spatial contaminant probabilities of occurrence of chlorinated hydrocarbons in an urban aquifer.

    PubMed

    Greis, Tillman; Helmholz, Kathrin; Schöniger, Hans Matthias; Haarstrick, Andreas

    2012-06-01

    In this study, a 3D urban groundwater model is presented which serves for calculation of multispecies contaminant transport in the subsurface on the regional scale. The total model consists of two submodels, the groundwater flow and reactive transport model, and is validated against field data. The model equations are solved applying finite element method. A sensitivity analysis is carried out to perform parameter identification of flow, transport and reaction processes. Coming from the latter, stochastic variation of flow, transport, and reaction input parameters and Monte Carlo simulation are used in calculating probabilities of pollutant occurrence in the domain. These probabilities could be part of determining future spots of contamination and their measure of damages. Application and validation is exemplarily shown for a contaminated site in Braunschweig (Germany), where a vast plume of chlorinated ethenes pollutes the groundwater. With respect to field application, the methods used for modelling reveal feasible and helpful tools to assess natural attenuation (MNA) and the risk that might be reduced by remediation actions.

  17. Monitoring the effect of poplar trees on petroleum-hydrocarbon and chlorinated-solvent contaminated ground water

    USGS Publications Warehouse

    Landmeyer, J.E.

    2001-01-01

    At contaminated groundwater sites, poplar trees can be used to affect groundwater levels, flow directions, and ultimately total groundwater and contaminant flux to areas downgradient of the trees. The magnitude of the hydrologic changes can be monitored using fundamental concepts of groundwater hydrology, in addition to plant physiology-based approaches, and can be viewed as being almost independent of the contaminant released. The affect of poplar trees on the fate of groundwater contaminants, however, is contaminant dependent. Some petroleum hydrocarbons or chlorinated solvents may be mineralized or transformed to innocuous compounds by rhizospheric bacteria associated with the tree roots, mineralized or transformed by plant tissues in the transpiration stream or leaves after uptake, or passively volatilized and rapidly dispersed or oxidized in the atmosphere. These processes also can be monitored using a combination of physiological- or geochemical-based field or laboratory approaches. When combined, such hydrologic and contaminant monitoring approaches can result in a more accurate assessment of the use of poplar trees to meet regulatory goals at contaminated groundwater sites, verify that these goals continue to be met in the future, and ultimately lead to a consensus on how the performance of plant-based remedial strategies (phytoremediation) is to be assessed.

  18. Sensitive detection of black powder by stand-alone ion mobility spectrometer with chlorinated hydrocarbon modifiers in drift gas.

    PubMed

    Liang, Xixi; Wang, Xin; Wang, Weiguo; Zhou, Qinghua; Chen, Chuang; Peng, Liying; Wen, Meng; Qu, Tuanshuai; Wang, Zhenxin; Zhao, Kun; Li, Jinghua; Li, Haiyang

    2014-04-01

    This paper introduces a simple method for selective and sensitive detection of black powder by adding chlorinated hydrocarbons in the drift gas instead of changing the structure of conventional ion mobility spectrometer (IMS). The function of chloride modifiers was to substitute Cl(-)(H₂O)n for [O₂⁻ (H₂O)(n)] in the drift region so as to avoid the overlap between O₂⁻ (H₂O)(n) and sulfur ion peaks. Among CH₂Cl₂, CHCl₃ and CCl₄, CCl₄ was chosen as the modifier due to the best peak-to-peak resolution and stability towards the fluctuation of modifier concentration. With 1.4 ppm CCl₄ as the modifier, the minimum detectable quantity of 0.1 ng for sulfur was achieved. Moreover, this method showed the ability for detection of common explosives at sub-nanogram level, such as black powder (BP), ammonium nitrate fuel oil (ANFO), 2,4,6-trinitrotoluene (TNT), and pentaerythritol tetranitrate (PETN). In summary, this method requiring no configuration modification has high sensitivity and selectivity, and consumes trace amount of modifier. And these characteristics make it easy to be adopted in current deployed IMS to detect black powder explosives.

  19. Comparison of purge and trap GC/MS and purgeable organic chloride analysis for monitoring volatile chlorinated hydrocarbons

    USGS Publications Warehouse

    Barber, Larry B.; Thurman, E. Michael; Takahashi, Yoshi; Noriega, Mary C.

    1992-01-01

    A combined field and laboratory study was conducted to compare purge and trap gas chromatography/mass spectrometry (PT-GC/MS) and purgeable organic chloride (POCl) analysis for measuring volatile chlorinated hydrocarbons (VCH) in ground water. Distilled-water spike and recovery experiments using 10 VCH indicate that at concentrations greater than 1 ??g/l recovery is more than 80 percent for both methods with relative standard deviations of about 10 percent. Ground-water samples were collected from a site on Cape Cod, Massachusetts, where a shallow unconfined aquifer has been contaminated by VCH, and were analyzed by both methods. Results for PT-GC/MS and POCl analysis of the ground-water samples were not significantly different (alpha = 0.05, paired t-test analysis) and indicated little bias between the two methods. Similar conclusions about concentrations and distributions of VCH in the ground-water contamination plume were drawn from the two data sets. However, only PT-GC/MS analysis identified the individual compounds present and determined their concentrations, which was necessary for toxicological and biogeochemical evaluation of the contaminated ground water. POCl analysis was a complimentary method for use with PT-GC/MS analysis for identifying samples with VCH concentrations below the detection limit or with high VCH concentrations that require dilution. Use of POCl as a complimentary monitoring method for PT-GC/MS can result in more efficient use of analytical resources.

  20. Identifying sources of chlorinated aliphatic hydrocarbons in a residential area in Italy using the integral pumping test method

    NASA Astrophysics Data System (ADS)

    Alberti, Luca; Lombi, Silvia; Zanini, Andrea

    2011-09-01

    The results of integral pumping tests (IPTs) performed in the city of Fabriano, Italy, are presented. The IPT methodology was developed by the European Union project INCORE, as a tool for groundwater investigation and source localization in contaminated areas. This methodology consists of a multiple-well pumping test in which the wells are positioned along a control plane downstream of suspected contaminant source zones and perpendicular to the mean groundwater flow direction. During the pumping, concentration time series of target contaminants are measured. In Fabriano, two control planes were realized to identify a chlorinated aliphatic hydrocarbon plume, to estimate the mass fluxes and draw up a ranked list of the main contamination sources. A numerical flow model was implemented to support the IPT design and to interpret the results. This study revealed low-level trichloroethylene contamination (concentration below 8 μg/l), tetrachloroethylene contamination (mean concentration up to 500 μg/l) and a mass flow rate of about 300 g/day. Through the application of the IPT method, the mean contaminant concentrations, the spatial distribution of concentration values along the control planes, and the total contaminant mass flow rates were evaluated, and the investigation area was reduced for further and deeper investigation activities.

  1. Impact of carbon, oxygen and sulfur content of microscale zerovalent iron particles on its reactivity towards chlorinated aliphatic hydrocarbons.

    PubMed

    Velimirovic, Milica; Larsson, Per-Olof; Simons, Queenie; Bastiaens, Leen

    2013-11-01

    Zerovalent iron (ZVI) abiotically degrades several chlorinated aliphatic hydrocarbons (CAHs) via reductive dechlorination, which offers perspectives for in situ groundwater remediation applications. The difference in reactivity between ZVI particles is often linked with their specific surface area. However, other parameters may influence the reactivity as well. Earlier, we reported for a set of microscale zerovalent iron (mZVI) particles the disappearance kinetic of different CAHs which were collected under consistent experimental conditions. In the present study, these kinetic data were correlated with the carbon, oxygen and sulfur content of mZVI particles. It was confirmed that not only the specific surface area affects the disappearance kinetic of CAHs, but also the chemical composition of the mZVI particles. The chemical composition, in addition, influences CAHs removal mechanism inducing sorption onto mZVI particles instead of dechlorination. Generally, high disappearance kinetic of CAHs was observed for particles containing less oxygen. A high carbon content, on the other hand, induced nonreactive sorption of the contaminants on the mZVI particles. To obtain efficient remediation of CAHs by mZVI particles, this study suggested that the carbon and oxygen content should not exceed 0.5% and 1% respectively. Finally, the efficiency of the mZVI particles may be improved to some extent by enriching them with sulfur. However, the impact of sulfur content on the reactivity of mZVI particles is less pronounced than that of the carbon and oxygen content.

  2. Hydrocarbons in oil residues on beaches of islands of Prince William Sound, Alaska

    USGS Publications Warehouse

    Kvenvolden, K.A.; Hostettler, F.D.; Rapp, J.B.; Carlson, P.R.

    1993-01-01

    Aliphatic and aromatic hydrocarbons were measured on oil residues from beaches on six islands in Prince William Sound, Alaska. In addition to altered products from the Exxon Valdez oil spill of 1989, we also found, at two widely separated locations, residues that are similar to each other but chemically distinct from the spilled oil. Terpanes, steranes, monoaromatic steranes, and carbon isotopic compositions of total extracts were most useful in correlating the altered products of the spilled oil. These same parameters revealed that the two non-Valdez samples are likely residues of oil originally produced in California. The results indicate that oil residues currently on the beaches of this estuary have at least two quite different origins.

  3. A sensitive extracto-photometric method for determination of residual chlorine in greywater.

    PubMed

    March, Juan G; Gual, Mateu; Simonet, Bartolomé M

    2004-01-01

    A new photometric method for chlorine determination based on the oxidative transformation of iodide to iodine and subsequent extraction in ethyl acetate has been developed. The effects of several chemical variables (pH, ionic strength, and iodide concentration) have been studied. Characteristics of the method were linear range 0-0.6 mg C12/L, limit of detection 5 microg Cl2/L, and coefficient of variation 0.6%. The method has been applied to greywater without previous sample treatment.

  4. [Compositions and residual properties of petroleum hydrocarbon in contaminated soil of the oilfields].

    PubMed

    Hu, Di; Li, Chuan; Dong, Qian-Qian; Li, Li-Ming; Li, Guang-He

    2014-01-01

    The aims of this study were to determine the compositions and residual properties of petroleum hydrocarbon in soil, as well as to identify the source and weathering degree of the pollution. A total of 5 producing wells in Gudao and Hekou oil producing region of Shengli oilfields were analyzed. More than 50 individual target compounds including straight-and branched-chain alkanes( n-alkanes, pristine and phytane) and polycyclic aromatic hydrocarbons (PAHs) in soil samples and crude oil were determined by gas chromatography-mass spectrometry (GC-MS). The percentages of chain alkanes and PAHs in total solvent extractable matters(TSEM) of soil samples were both much lower than those in the crude oil samples. The compositions of petroleum hydrocarbon in soil samples differed from those in crude oil, which indicated the n-alkanes with carbon numbers <12 were much easier to lose in contrast to the n-alkanes with high carbon numbers. With n-octadecane/phytane as index for the weathering rate of oil contaminated soils, the relationship between the index and petroleum hydrocarbon compounds was analyzed using principal component analysis (PCA). The results showed that the n-alkanes with carbon numbers > 33 and the PAHs with rings between 3 and 5 were much harder to degrade. PCA of 4 indexes for source identification revealed more than 50% of the soil samples were polluted by crude oil, which needs more attention during remediation.

  5. Genetic Engineering of Plants to Improve Phytoremediation of Chlorinated Hydrocarbons in Groundwater

    SciTech Connect

    Strand, Stuart E.

    2004-12-01

    I. Mechanism of halogenated hydrocarbon oxidation We are using poplar culture cells to determine the pathway of TCE metabolism. In our earlier work, we found that trichloroethanol (TCEOH) is a major early intermediate. Our studies this year have focused on the steps that follow this toxic intermediate. We did several experiments to track the disappearance of TCEOH after the cells were removed from TCE. We could conclude that TCEOH is not an end-product but is rapidly degraded. Six flasks of poplar liquid suspension cells were exposed to a level of 50 {micro}g/ml TCE for three days. Three of the cultures were subjected to MTBE extractions to quantify the levels of TCEOH produced. The cells of the remaining three cultures were then pelleted and resuspended in fresh medium. After three more days, these were also subjected to MTBE extractions. The samples were analyzed by GC-ECD. After the three days of further metabolism, an average of 91% of the trichloroethanol was gone. When similar experiments were done with intact plants and both free and conjugated TCEOH were quantified, a similar rapid decline in both forms was seen (Shang, 2001). Therefore, it seems probable that similar mechanisms are taking place in both poplar suspension cells and whole poplar plants, so we continued to do our studies with the suspension cells. Metabolism of trichloroethanol may go through trichloroacetic acid (TCAA) prior to dehalogenation. To test this possibility, we exposed cells to TCE and analyzed for TCAA over time. The cultures were analyzed after 4, 5, 6, and 14 days from TCE exposure. We did not detect any significant amount of TCAA above the background in undosed cells. To determine if trichloroethanol itself is directly dehalogenated, we analyzed TCE-exposed cells for the presence of dichloroethanol. Undosed cells did not have any of the DCEOH peak but TCE-dosed cells that produced the highest levels of trichloroethanol did have a small DCEOH peak. Cultures that did not produce

  6. In Vitro Transformation of Chlorinated Parabens by the Liver S9 Fraction: Kinetics, Metabolite Identification, and Aryl Hydrocarbon Receptor Agonist Activity.

    PubMed

    Terasaki, Masanori; Wada, Takeshi; Nagashima, Satoshi; Makino, Masakazu; Yasukawa, Hiro

    2016-01-01

    We investigated the kinetics of in vitro transformation of a dichlorinated propyl paraben (2-propyl 3,5-dichloro-4-hydroxybenzoate; Cl2PP) by the rat liver S9 fraction and assessed the aryl hydrocarbon receptor (AhR) agonist activity of the metabolite products identified in HPLC and GC/MS analysis and by metabolite syntheses. The results indicated that the chlorination of Cl2PP reduced its degradation rate by approximately 40-fold. Two hydroxylated metabolite products showed AhR agonist activity of up to 39% of that of the parent Cl2PP when assessed in a yeast (YCM3) reporter gene assay. The determination of the metabolic properties of paraben bioaccumulation presented here provides further information on the value of risk assessments of chlorinated parabens as a means to ensure human health and environmental safety. PMID:27250800

  7. A Model to Predict Total Chlorine Residue in the Cooling Seawater of a Power Plant Using Iodine Colorimetric Method

    PubMed Central

    Wang, Jih-Terng; Chen, Ming-Hui; Lee, Hung-Jen; Chang, Wen-Been; Chen, Chung-Chi; Pai, Su-Cheng; Meng, Pei-Jie

    2008-01-01

    A model experiment monitoring the fate of total residue oxidant (TRO) in water at a constant temperature and salinity indicated that it decayed exponentially with time, and with TRO decaying faster in seawater than in distilled water. The reduction of TRO by temperature (°K) was found to fit a curvilinear relationship in distilled water (r2 = 0.997) and a linear relationship in seawater (r2 = 0.996). Based on the decay rate, flow rate, and the length of cooling water flowing through at a given temperature, the TRO level in the cooling water of a power plant could be estimated using the equation developed in this study. This predictive model would provide a benchmark for power plant operators to adjust the addition of chlorine to levels necessary to control bio-fouling of cooling water intake pipelines, but without irritating ambient marine organisms. PMID:19325768

  8. Quantification of temperature impacts on the dissolution of chlorinated hydrocarbons into groundwater

    NASA Astrophysics Data System (ADS)

    Koproch, Nicolas; Popp, Steffi; Köber, Ralf; Beyer, Christof; Bauer, Sebastian; Dahmke, Andreas

    2016-04-01

    -water contact areas. Thirdly, heatable 2D-tanks (40 cm x 25 cm x 10 cm) homogenously filled with quartz sand and percolated by distilled H2O were used to investigate the dissolution behavior and plume development of TCE from a residual source zone (5 cm x 5 cm x 10 cm) at 10-70°C. Using NAPL source zone saturation of 5% (Case A) and 20% (Case B) two exemplary cases of a depleted and a fresh source zone were investigated. TCE outflow concentrations in case A increased continuously with increasing temperature, but were controlled by the temperature-dependent solubility in Case B. The experimental results showed that the TCE mass transfer rate has a minimum at about 40°C, if dissolution is non-rate limited and a continuous increase with increasing temperature for rate-limited systems. Implementation of temperature dependent NAPL dissolution and two different blob categories with different mass transfer rate coefficients in the OpenGeoSys code proved successful in reproducing the experimental results. Acknowledgments: The presented work is part of the ANGUS+ project (03EK3022) funded by the German Ministry of Education and Research (BMBF).

  9. Residues of petroleum hydrocarbons in tissues of sea turtles exposed to the IXTOC I oil spill

    USGS Publications Warehouse

    Hall, R.J.; Belisle, A.A.; Sileo, L.

    1983-01-01

    Sea turtles found dead when the Ixtoc I oil spill reached Texas waters were necropsied and tissues were analyzed for residues of petroleum hydrocarbons. Two of the three turtles were in poor flesh, but had no apparent oil-caused lesions. There was evidence of oil in all tissues examined and indications that the exposure had been chronic. Comparisons with results of studies done on birds indicate consumption of 50,000 ppm or more of oil in the diet. Some possible mechanisms of mortality are suggested.

  10. Residues of petroleum hydrocarbons in tissues of sea turtles exposed to the Ixtoc I oil spill

    SciTech Connect

    Hall, R.J.; Belisle, A.A.; Sileo, L.

    1983-04-01

    Sea turtles found dead when the Ixtoc I oil spill reached Texas waters were necropsied and tissues were analyzed for residues of petroleum hydrocarbons. Two of three turtles were in poor flesh, but had no apparent oil-caused lesions. There was evidence of oil in all tissues examined and indications that the exposure had been chronic. Comparisons with results of studies done on birds indicate consumption of 50,000 ppm or more of oil in the diet. Some possible mechanisms of mortality are suggested.

  11. EXPECTED EFFECTS OF RESIDUAL CHLORINE AND NITROGEN IN SEWAGE EFFLUENT ON THE ESTUARINE ECOSYSTEM OF GREENWICH COVE, RI: AN ENERGY SYSTEMS AND RISK ASSESSMENT OF EFFECTS

    EPA Science Inventory

    Physical, toxicological, and energy systems modeling were combined to make estimates of likely ecosystem-level effects due to residual chlorine in sewage effluent. The energy systems model also allowed us to make estimates of the effects of nutrient loading on the estuary both se...

  12. Heavy metal and hydrocarbon residues in tissue and blood of beef steers bedded on waste newspapers

    SciTech Connect

    Comerford, J.W.

    1992-07-01

    There are over 3 million tons of waste newspaper generated annually in Pennsylvania alone. This provides a significant disposal problem for many municipalities who are confronted with dwindling options for solid waste disposal. Previous studies have identified several of the potential advantages of the material as a bedding material for livestock. With over 1 million beef and dairy cattle in the state, the potential use of newspaper as bedding is important. Of concern, however, is the effect of the chemical composition of the paper on animals which have the opportunity to consume it, and subsequent entry of undesirable residues into the food chain. Metals such as cadmium, lead, mercury and copper are known to exist in relatively high quantities in newsprint from the ink used in printing. Naphthalene and other aromatic hydrocarbons which are found in coal tar and synthetic and natural crude oils are known to accumulate in marine life and are absorbed by humans after consumption. A preliminary report indicated beef steers bedded on newspaper did consume varying amounts of the material. Few studies have determined if residues of heavy metals or organic compounds are found in the carcasses of animals continuously bedded on newspaper. The objectives of this study were to determine the levels of cadmium, copper, lead, mercury and certain aromatic hydrocarbons in the blood and liver of feedlot cattle bedded continuously on waste newspaper or sawdust. 4 refs., 3 tabs.

  13. CHLORINATED SOLVENT CONTAMINATED SOILS AND GROUNDWATER: FIELD APPLICATION OF THE SOLVENT EXTRACTION RESIDUAL BIOTREATMENT TECHNOLOGY

    EPA Science Inventory

    A pilot scale demonstration of the Solvent Extraction Residual Biotreatment (SERB) technology was conducted at the former Sage's Dry Cleaner site in Jacksonville, FL. The SERB technology is a treatment train approach to complete site restoration, which combines an active in situ...

  14. Implications of treating water containing polynuclear aromatic hydrocarbons with chlorine: a gas chromatographic-mass spectrometric study.

    PubMed Central

    Oyler, A R; Liukkonen, R J; Lukasewycz, M K; Cox, D A; Peake, D A; Carlson, R M

    1982-01-01

    The products of aqueous chlorination reactions of 1-methylnaphthalene, fluorene, dibenzofuran, anthracene, phenanthrene, 1-methylphenanthrene, fluoranthene, and pyrene have been determined. The conditions employed for these reactions approximated those that might be encountered in water treatment facilities. Reactions at pH greater than 6 tended to produce oxygenated products (epoxides, phenols, quinones, etc.), and reactions at pH less than 6 tended to produce both oxygenated (quinones) and chlorinated products. PMID:7151769

  15. Distributions and fate of chlorinated pesticides, biomarkers and polycyclic aromatic hydrocarbons in sediments along a contamination gradient from a point-source in San Francisco Bay, California

    USGS Publications Warehouse

    Pereira, W.E.; Hostettler, F.D.; Rapp, J.B.

    1996-01-01

    The distribution and fate of chlorinated pesticides, biomarkers, and polycyclic aromatic hydrocarbons (PAHs) in surficial sediments along a contamination gradient in the Lauritzen Canal and Richmond Harbor in San Francisco Bay was investigated. Compounds were identified and quantified using gas chromatography-ion trap mass spectrometry. Biomarkers and PAHs were derived primarily from weathered petroleum. DDT was reductively dechlorinated under anoxic conditions to DDD and several minor degradation products, DDMU, DDMS, and DDNU. Under aerobic conditions, DDT was dehydrochlorinated to DDE and DBP. Aerobic degradation of DDT was diminished or inhibited in zones of high concentration, and increased significantly in zones of lower concentration: Other chlorinated pesticides identified in sediment included dieldrin and chlordane isomers. Multivariate analysis of the distributions of the DDTs suggested that there are probably two sources of DDD. In addition, DDE and DDMU are probably formed by similar mechanisms, i.e. dehydrochlorination. A steep concentration gradient existed from the Canal to the Outer Richmond Harbor, but higher levels of DDD than those found in the remainder of the Bay indicated that these contaminants are transported on particulates and colloidal organic matter from this source into San Francisco Bay. Chlorinated pesticides and PAHs may pose a potential problem to biota in San Francisco Bay.

  16. Characterisation of chlorinated, brominated and mixed halogenated dioxins, furans and biphenyls as potent and as partial agonists of the Aryl hydrocarbon receptor.

    PubMed

    Wall, Richard J; Fernandes, Alwyn; Rose, Martin; Bell, David R; Mellor, Ian R

    2015-03-01

    The Aryl hydrocarbon receptor (AhR) binds a variety of chlorinated and brominated dioxins, furans and biphenyls. Mixed halogenated variants have been recently identified in food at significant levels but full characterisation requires potency data in order to gauge their impact on risk assessment. Rat H4IIE and human MCF-7 cells were treated with various mixed halogenated ligands. Antagonist properties were measured by treating cells with various concentrations of TCDD in the presence of EC25 of the putative antagonist. Measurement of CYP1A1 RNA was used to quantify the potency of agonism and antagonism. The PXDDs were found to be slightly less potent than the corresponding fully chlorinated congeners with the exception of 2-B,3,7,8-TriCDD which was 2-fold more potent than TCDD. PXDFs and non-ortho-PXBs were found to be more potent than their chlorinated congeners whilst several mono-ortho-substituted PXBs were shown to have partial agonistic properties. REPs were produced for a range of mixed halogenated AhR-activating ligands providing a more accurate estimation of potency for risk assessment. Several environmentally abundant biphenyls were shown to be antagonists and reduce the ability of TCDD to induce CYP1A1. The demonstration of antagonism for AhR ligands represents a challenge for existing REP risk assessment schemes for AhR ligands.

  17. Chlorinated hydrocarbons and mercury in sediments, red-winged blackbirds (Agelaius phoeniceus) and tree swallows (Tachycineta bicolor) from wetlands in the Great Lakes-St. Lawrence River basin

    SciTech Connect

    Bishop, C.A.; Koster, M.D.; Chek, A.A.; Hussell, D.J.T.; Jock, K.

    1995-03-01

    In 1991, the authors collected red-winged blackbird (Agelauis phoeniceus) eggs and tree swallow (Tachycineta bicolor) eggs and nestlings, and sediment samples from 2 wetland sites in the Great lakes and St. Lawrence River basin. They analyzed for chlorinated hydrocarbons and total mercury and found that biota contained contaminant concentrations which were one to two orders of magnitude above those in sediments. Maximum concentrations of contaminants were found in Akwesasne, St. Lawrence river (PCBs = 18,558.8 ng/g in red-winged blackbird eggs, oxychlordane = 58.8/g and mirex = 40.1 ng/g in tree swallow eggs); Mud Creek, Lake Erie and Cootes Paradise. Despite the migratory habits of red-winged blackbirds and tree swallows, agreement among biota and sediment in geographic variation of contaminant concentrations supports the use of these animals as biomonitors of persistent chemicals. Although chlorinated hydrocarbon concentrations in red-winged blackbird eggs were significantly correlated with sediment contamination, the local nature of the tree swallow chick diet suggests that nestlings would be the best indicator of local contaminant trends.

  18. Chlorinated dibenzo-p-dioxin and dibenzofuran residue levels in food. Final report

    SciTech Connect

    Stanley, J.S.; Bauer, K.M.

    1989-10-26

    The chemical analysis of selected foods was conducted to provide an estimate of the residue levels of PCDDs and PCDFs. The foodstuffs included saltwater fish, freshwater fish, beef, chicken, pork, bovine milk, and eggs. The foodstuffs were collected from San Francisco and Los Angeles. Emphasis was placed on the collection of foodstuffs of California origin. Individual foods collected from multiple sites within San Francisco and Los Angeles were composited for analysis of the residue levels. Detectable levels of PCDDs and PCDFs were identified in all but the egg samples that were analyzed. Overall, the freshwater fish composites were found to have the highest incidence of detectable levels. The order of highest to lowest incidence of detection follows: freshwater fish > saltwater fish > pork and chicken > beef and milk > eggs. All data were generated from a sample size of approximately 10 g of extractable fatty materials. All data are presented to reflect lipid or fat concentrations such that extrapolation with other data bases can be achieved.

  19. Evaluation of approaches to quantify total residual oxidants in ballast water management systems employing chlorine for disinfection.

    PubMed

    Zimmer-Faust, Amity G; Ambrose, Richard F; Tamburri, Mario N

    2014-01-01

    With the maturation and certification of several ballast water management systems that employ chlorine as biocide to prevent the spread of invasive species, there is a clear need for accurate and reliable total residual oxidants (TRO) technology to monitor treatment dose and assure the environmental safety of treated water discharged from ships. In this study, instruments used to measure TRO in wastewater and drinking water applications were evaluated for their performance in scenarios mimicking a ballast water treatment application (e.g., diverse hold times, temperatures, and salinities). Parameters chosen for testing these technologies in the past do not reflect conditions expected during ballast water treatment. Salinity, temperature, and oxidant concentration all influenced the response of amperometric sensors. Oxidation reduction potential (ORP) sensors performed more consistently than amperometric sensors under different conditions but it may be difficult to correlate ORP and TRO measurements for the multitude of biogeochemical conditions found naturally in ballast water. N,N-diethyl-p-phenylenediamine (DPD) analyzers and amperometric sensors were also tested under intermittent sampling conditions mimicking a ballasting scenario, with cyclical dosage and discharge operations. When sampling was intermittent, amperometric sensors required excessive response and conditioning times, whereas DPD analyzers provided reasonable estimates of TRO under the ballasting scenario.

  20. A New On-Line Detecting Apparatus of the Residual Chlorine in Disinfectant for Fresh-Cut Vegetables

    NASA Astrophysics Data System (ADS)

    Hu, Chao; Su, Shu-Qiang; Li, Bao-Guo; Liu, Meng-Fang

    With the fast development of modern food and beverage industry, fresh-cut vegetables have wider application than before. During the process of sterilization in fresh-cut vegetables, the concentration of chloric disinfectant is usually so high that the common sensor can't be used directly on the product line. In order to solve this problem, we have invented a new detecting apparatus which could detect high concentration of chloric disinfectant directly. In this paper, the working principle, main monitor indicators, application and technical creations of the on-line apparatus have been discussed, and we also carried on the experimental analysis for its performance. The actual demands in factory could be met when the detecting flux is 2L/min, the dilution ratio is 15 and input amount of the disinfectant is 200ml per time, the max of the detecting deviation achieves ±4.8ppm(mg/L). The main detecting range of residual chlorine is 0~300ppm.

  1. Residue level of polycyclic aromatic hydrocarbons in Japanese paddy soils from 1959 to 2002.

    PubMed

    Honda, K; Mizukami, M; Ueda, Y; Hamada, N; Seike, N

    2007-08-01

    The residue level of 21 polycyclic aromatic hydrocarbons (PAHs) and the temporal changes in this level were investigated in paddy soils collected from particular experimental sites in Japan from 1959 to 2002. The average total PAH concentration in all the samples was 496 microg kg(-1), and it ranged from 52.9 to 2180 microg kg(-1). The residue level of the PAHs was the highest during the 1960s, rapidly decreased during the 1970s, and remained almost constant thereafter. Relatively high PAH concentrations were observed in soils from areas that experienced heavy snowfall and that had relatively low air temperature. The predominant PAHs were phenanthrene, fluoranthene, naphthalene, and pyrene, and their concentration overall and in relation to that of the total PAHs decreased each year since the 1960s. Similarities in the PAH profiles among the locations were determined using the concentration correlation matrix and cluster analysis, and ratios of the levels of specific PAH pairs were also calculated to determine their origin. The collected data suggested that the origins of soil PAHs changed chronologically from the burning of agricultural wastes such as stubble before the mid-1970s to the combustion of fossil fuel and its secondary products after the mid-1970s.

  2. Biodegradation pattern of hydrocarbons from a fuel oil-type complex residue by an emulsifier-producing microbial consortium.

    PubMed

    Nievas, M L; Commendatore, M G; Esteves, J L; Bucalá, V

    2008-06-15

    The biodegradation of a hazardous waste (bilge waste), a fuel oil-type complex residue from normal ship operations, was studied in a batch bioreactor using a microbial consortium in seawater medium. Experiments with initial concentrations of 0.18 and 0.53% (v/v) of bilge waste were carried out. In order to study the biodegradation kinetics, the mass of n-alkanes, resolved hydrocarbons and unresolved complex mixture (UCM) hydrocarbons were assessed by gas chromatography (GC). Emulsification was detected in both experiments, possibly linked to the n-alkanes depletion, with differences in emulsification start times and extents according to the initial hydrocarbon concentration. Both facts influenced the hydrocarbon biodegradation kinetics. A sequential biodegradation of n-alkanes and UMC was found for the higher hydrocarbon content. Being the former growth associated, while UCM biodegradation was a non-growing process showing enzymatic-type biodegradation kinetics. For the lower hydrocarbon concentration, simultaneous biodegradation of n-alkanes and UMC were found before emulsification. Nevertheless, certain UCM biodegradation was observed after the medium emulsification. According to the observed kinetics, three main types of hydrocarbons (n-alkanes, biodegradable UCM and recalcitrant UCM) were found adequate to represent the multicomponent substrate (bilge waste) for future modelling of the biodegradation process. PMID:17997031

  3. Assessment of the intrinsic bioremediation capacity of an eutrophic river sediment polluted by discharging chlorinated aliphatic hydrocarbons: a compound-specific isotope approach.

    PubMed

    Kuhn, Thomas K; Hamonts, Kelly; Dijk, John A; Kalka, Harald; Stichler, Willibald; Springael, Dirk; Dejonghe, Winnie; Meckenstock, Rainer U

    2009-07-15

    At a field site in the industrial area of Vilvoorde, Belgium, we investigated the capacity of the indigenous microbial community of a eutrophic river sediment to biodegrade chlorinated aliphatic hydrocarbons (CAHs) originating from discharging, polluted groundwater using a compound-specific isotope approach. We specifically targeted the site's major pollutants cis-1,2-dichloroethene (cis-DCE) and vinyl chloride (VC). Analysis of Rayleigh correlation plots enabled us to assess the extent to which microbial and abiotic natural attenuation processes contributed to the mitigation of a pollution of the surface water due to discharging CAH-contaminated groundwater. Our results provide evidence for (i) the occurrence of biodegradation of cis-DCE and VC by reductive dechlorination in parts of the aquifer and at several positions in the river sediment (ii) the presence of river sediment zones exhibiting attenuation of chloroethenes by a combination of biodegradation and dilution through unpolluted water, (iii) the existence of zones in the river sediment lacking significant biodegradation, and thus (iv) a pronounced spatial heterogeneity in the occurrence and extent of biodegradation in the aquifer and river sediment. We conclude that at many investigated positions in the river sediment the indigenous microbial community failed to facilitate complete biodegradation of the groundwater-sourced chloroethenes. The overall intrinsic bioremediation capacity of the river sediment was thus not high enough to completely prevent the release of these pollutants into the surface water. These findings and conclusions are thus in agreement with those of our companion paper (1), which investigated the river sediments at the Vilvoorde study site by a combination of stable hydrogen and oxygen isotope analysis of water and the detection of chlorinated aliphatic hydrocarbons (CAHs) and their dechlorination products.

  4. A comparison of the concentrations of certain chlorinated hydrocarbons and polychlorinated biphenyls in bone marrow and fat tissue of children and their concentrations in breast milk

    SciTech Connect

    Scheele, J.; Teufel, M.; Niessen, K.H.

    1995-12-31

    Chlorinated hydrocarbon (CHC) and polychlorinated biphenyl (PCB) concentrations in the bone marrow of 57 children were compared with the concentrations in adipose tissue of 50 children and the concentrations in breast milk in the Federal Republic of Germany from 1984 to 1991. The concentrations of hexachlorobenzene (HCB), the dichlorodiphenyl-trichlorethane (DDT)-metabolites, and polychlorinated biphenyl (PCB) congeners no. 138 and no. 153 were increased threefold, while the concentrations of several hexachloro-cyclohexane (HCH)-isomers and PCB congener no. 180 were only increased two fold. Because breast feeding is the primary source of CHC and PCB in toddlers and infants we also compared the concentrations in bone marrow of children with the concentrations in breast milk and found approximately fourfold higher concentrations for the most highly chlorinated PCB congener no. 180, but only threefold higher concentrations for PCB 138 and 153 and the DDT-metabolites. The concentrations of {beta}-HCH and HCB were only slightly higher in bone marrow. 15 refs., 2 figs.

  5. Experimental and theoretical studies into the formation of C4-C6 products in partially chlorinated hydrocarbon pyrolysis systems: a probabilistic approach to congener-specific yield predictions.

    PubMed

    McIntosh, Grant J; Russell, Douglas K

    2014-09-25

    This work presents a study of the pyrolytic formation of vinylacetylene and benzene congeners formed from chlorinated hydrocarbon precursors, a complex, multipath polymerization system formed in a monomer-rich environment. (Co-)pyrolyses of dichloro- and trichloroethylene yield a rich array of products, and assuming a single dominant underlying growth mechanism, this (on comparing expected and observed products) allows a number of potentially competing channels to C4 and C6 products to be ruled out. Poor congener/isomer descriptions rule out even-carbon radical routes, and the absence of C3 and C5 products rule out odd-carbon processes. Vinylidenes appear unable to describe the increased reactivity of acetylenes with chlorination noted in our experiments, leaving molecular acetylene dimerization processes and, in C6 systems, the closely related Diels-Alder cyclization as the likely reaction mechanism. The feasibility of these routes is further supported by ab initio calculations. However, some of the most persuasive evidence is provided by congener-specific yield predictions enabled by the construction of a probability tree analogue of kinetic modeling. This approach is relatively quick to construct, provides surprisingly accurate predictions, and may be a very useful tool in screening for important reaction channels in poorly understood congener- or isomer-rich reaction systems.

  6. Novel oxidative electrophilic coupling reactions of phenoxazine derivatives with MBTH and their applications to spectrophotometric determination of residual chlorine in drinking water and environmental water samples.

    PubMed

    Al-Okab, Riyad Ahmed; Syed, Akheel Ahmed

    2009-10-15

    Novel, sensitive and rapid spectrophotometric methods, using phenoxazine (PNZ), 2-chlorophe-noxazine (CPN) and 2-trifluoromethylphenoxazine (TPN) as chromogenic reagents for the determination of residual chlorine are proposed. The methods are based on the reduction of chlorine by an electrophilic coupling reagent, 3-methyl-2-benzothiazoline hydrazono hydrochloride hydrate (MBTH) in mild hydrochloric acid medium and subsequent coupling with PNZ, CPN or TPN. The blue color formed in the reaction showed maximum absorbance at 680-690 nm and obeyed Beer's law over the range 0.1-2.2 microg ml(-1). The molar absorptivity values with PNZ, CPN and TPN were 2.80 x 10(4), 2.67 x 10(4) and 1.91 x 10(4) l mol(-1)cm(-1) and Sandell's sensitivity values were 0.028, 0.027 and 0.028 microg cm(-2) respectively. The proposed methods were successfully applied in the determination of residual chlorine in drinking water and environmental water samples. The performance of proposed methods was evaluated in terms of Student's t-test and variance ratio F-test which indicated the significance of proposed methods over the standard spectrophotometric method.

  7. The total and freely dissolved polycyclic aromatic hydrocarbons content in residues from biogas production.

    PubMed

    Stefaniuk, Magdalena; Oleszczuk, Patryk

    2016-01-01

    In the situation of increasing agricultural utilization of residues from biogas production (RBP) it is important to determine the concentration of contaminants, which could occur in these materials. The group of contaminants that requires special attention are polycyclic aromatic hydrocarbons (PAH). The objective of the study was to determine the total and freely dissolved (Cfree) of PAHs in RBP from 6 different biogas plants operating under various temperature conditions and without or with the separation into the solid and liquid fractions. The freely dissolved PAHs were determined using polyoxymethylene (POM method). The total content of the Σ16 PAHs in RBP varied from 449 to 6147 μg/kgdw, while that of Cfree PAHs was at the level from 57 to 653 ng/L. No significant differences were noted in the content of the Σ16 PAHs (total) between the solid and the liquid fractions. This indicates that in the course of the separation, the PAHs are distributed proportionally between the fractions. However in the case of Cfree, PAHs content in the solid fraction was over twice as high as in the liquid fraction. This was probably due to the greater affinity of the particles present in the liquid fraction to the analysed PAHs than to the particles of the solid fraction. Higher affinity to liquid fraction was also confirmed by the distribution coefficients KTOC determined on the basis of Cfree.

  8. Chlorinated hydrocarbons in livers of American mink (Mustela vison) and river otter (Lutra canadensis) from the Columbia and Fraser River Basins, 1990-1992

    USGS Publications Warehouse

    Elliott, J.E.; Henny, Charles J.; Harris, M.L.; Wilson, L.K.; Norstrom, R.J.

    1999-01-01

    We investigated chlorinated hydrocarbon contaminants in aquatic mustelid species on the Fraser and Columbia Rivers of northwestern North America. Carcasses of river otter (Lutra canadensis) (N=24) and mink (Mustela vison) (N=34) were obtained from commercial trappers during the winters of 1990-91 and 1991a??92. Pooled liver samples were analyzed for organochlorine pesticides, polychlorinated biphenyls (PCBs), including non-ortho congeners, polychlorinated dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs). Most samples contained detectable concentrations of DDE, PCBs, although there was substantial variability in patterns and trends among neighboring samples. Concentrations of DDE were in some mink and several otter samples from the lower Columbia River elevated (to 4700 g/kg wet weight); excluding one mink sample from the Wenatchee area, mean DDE levels generally decreased between 1978a??79 and 1990a??92. PCBs were present in all samples. PCB concentrations in otter livers collected from the lower Columbia were ten-fold lower than measured a decade previously; nevertheless, a sample taken near Portland had a mean concentration of 1500 g/kg, within a range of concentrations associated with reproductive effects in captive mink. Concentrations of 2,3,7,8-TCDD and TCDF were generally below detection limits, except for one otter collected near a pulp mill at Castlegar, on the upper Columbia, with 11 ng TCDD/kg in liver. Elevated concentrations of higher chlorinated PCDD/Fs, probably resulting from use of chlorophenolic wood preservatives, were found in both species; one otter sample from the lower Columbia had 2200 ng OCDD/kg. International TCDD toxic equivalent levels in mink (31 ng/kg) and otter (93 ng/kg) from the lower Columbia River approached toxicity thresholds for effects on reproduction in ranch mink.

  9. Transformation of chlorinated hydrocarbons using aquocobalamin or coenzyme F{sub 430} in combination with zero-valent iron

    SciTech Connect

    Morra, M.J.; Borek, V.; Koolpe, J.

    2000-06-01

    More effective methods are necessary for the remediation of soils, sediments, and ground waters contaminated with halogenated organic compounds. The authors objective was to determine the feasibility and utility of using a tetrapyrrole-Fe(0) mixture for reductive dehalogenation of synthetic organic contaminants. Aquocobalamin or coenzyme F{sub 430} was combined with Fe(0) in aqueous systems containing either a single chlorinated compound or mixtures of chlorinated compounds, and substrate disappearance was monitored using gas chromatography-mass spectrometry (GC-MS). Zero-valent iron effectively dehalogenated CCl{sub 4} at low to neutral pH values, while increases in CCl{sub 4} dehalogenation resulting from inclusion of tetrapyrrole catalysts along with Fe(0) occurred only at basic pH values. Rates of CCl{sub 4} disappearance increased with additional aquocobalamin, but reached a maximum and decreased at higher aquocobalamin concentrations. overall dehalogenation rates may thus be a function of Fe(0)'s limited reactive surface area. There was a trend for both tetrapyrrole catalysts to promote the disappearance of halogenated compounds in a mixed substrate containing 20 compounds. Studies with five individual substrates likewise showed trends for increased substrate removal with F{sub 430} beyond that for Fe(0) alone. This increase is most important for compounds such as 1,2-dichloroethane and 1,4-dichlorobenzene that are not readily dehalogenated by Fe(0). Chloride concentrations in the reaction mixtures indicated that reductive dehalogenation was the dominant process responsible for substrate disappearance. Use of a combination of aquocobalamin or coenzyme F{sub 430} and Fe(0) may effectively promote dehalogenation, thus producing fewer products and more complete dehalogenation of the target substrates than can be achieved using only one of the abiotic reductants alone.

  10. Bugs digest chlorinated organics

    SciTech Connect

    Not Available

    1993-02-01

    This article describes a new bioreactor that uses a consortium of aerobic bacteria to biodegrade chlorinated aromatic hydrocarbons. Methanotrophic bacteria are cultivated for their MMO enzyme. After the MMO enzyme breaks down the chlorinated organics by oxidation, non-methanotrophic bacteria consume the byproducts. Pilot-scale testing has demonstrated successful treatment of groundwater containing coal-tar constituents, toluene, trichloroethylene, vinyl chlorides, chlorobenzene, and methyl methacrylate from three Superfund sites.

  11. Comparison of two extraction methods for the analysis of petroleum hydrocarbon residues in mallard duck eggs by GC and GC-MS

    USGS Publications Warehouse

    Belisle, A.A.; Gay, M.L.; Coon, N.C.

    1981-01-01

    Hydrocarbon residues in pooled eggs from a mallard duck on a diet of 25,000 ppm South Louisiana crude oil were compared after cleanup with and without saponification. The saponification procedure yielded superior reproducibility and extraction efficiency

  12. Comparison of two extraction methods for the analysis of petroleum hydrocarbon residues in mallard duck eggs by GC and GC-MS. [NONE

    SciTech Connect

    Belisle, A.A.; Gay, M.L.; Coon, N.C.

    1981-01-01

    Hydrocarbon residues in pooled eggs from a mallard duck on a diet of 25,000 ppm South Louisiana crude oil were compared after cleanup with and without saponification. The saponification procedure yielded superior reproducibility and extraction efficiency..

  13. Breakpoint chlorination curves of greywater.

    PubMed

    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

  14. Breakpoint chlorination curves of greywater.

    PubMed

    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.

  15. Quantification of biotransformation of chlorinated hydrocarbons in a biostimulation study: Added value via stable carbon isotope analysis

    NASA Astrophysics Data System (ADS)

    Hirschorn, Sarah K.; Grostern, Ariel; Lacrampe-Couloume, Georges; Edwards, Elizabeth A.; MacKinnon, Leah; Repta, Cory; Major, David W.; Sherwood Lollar, Barbara

    2007-12-01

    Stable carbon isotope analysis of chlorinated aliphatic compounds was performed at an in situ biostimulation pilot test area (PTA) at a site where 1,2-dichloroethane (1,2-DCA) and trichloroethene (TCE) were present in groundwater. Chlorinated products of TCE reductive dechlorination ( cis-dichloroethene (cDCE) and vinyl chloride (VC)) were present at concentrations of 17.5 to 126.4 μmol/L. Ethene, a potential degradation product of both 1,2-DCA dihaloelimination and TCE reductive dechlorination was also present in the PTA. Emulsified soybean oil and lactate were added as electron donors to stimulate anaerobic dechlorination in the PTA. Stable carbon isotope analysis provided evidence that dechlorination was occurring in the PTA during biostimulation, and a means of monitoring changes in dechlorination efficiency over the 183 day monitoring period. Stable carbon isotope analysis was also used to determine if ethene production in the PTA was due to dechlorination of TCE, 1,2-DCA, or both. Fractionation factors ( α) were determined in the laboratory during anaerobic biotransformation of 1,2-DCA via a dihaloelimination reaction in four separate enrichment cultures. These α values (as well as the previously published ranges of α for the dechlorination of TCE, cDCE and 1,2-DCA) were used, along with isotopic values measured during the pilot test, to derive quantitative estimates of biotransformation during the pilot test. Dechlorination was found to account for 10.7 to 35.9%, 21.9 to 74.9%, and 54.4 to 67.8% of 1,2-DCA, TCE and cDCE concentration loss respectively in the PTA. Stable carbon isotope analysis indicates that dechlorination of 1,2-DCA, TCE and cDCE were all significant processes during the pilot test, while ethene production during the pilot test was dominated by 1,2-DCA dihaloelimination. This study demonstrates how stable carbon isotope analysis can provide more conservative estimates of the extent of biotransformation than do conventional protocols. In

  16. Chlorinated hydrocarbon contaminants in blood of black and turkey vultures from Savannah River Site, South Carolina, USA.

    PubMed

    Senthil Kumar, Kurunthachalam; Bowerman, William W; DeVault, Travis L; Takasuga, Takumi; Rhodes, Olin E; Lehr Brisbin, I; Masunaga, Shigeki

    2003-10-01

    Blood of adult and juvenile black and turkey vultures in the Savannah River Site of South Carolina, USA was analyzed for the presence of 2,3,7,8-chlorine substituted polychlorinated dibenzo-p-dioxins (2,3,7,8-PCDDs), dibenzofurans (2,3,7,8-PCDFs), -dioxin-like and -di-ortho polychlorinated biphenyls. Concentration ranges of 2,3,7,8-PCDD/DFs in blood of black and turkey vultures were 14.2-34.6 and 8.7-56.2 pg/ml wet wt., respectively. Dioxin-like PCBs were in the ranges of 815-4627 and 753-3611 pg/ml wet wt. respectively, in black and turkey vultures. Considerable concentrations of two congeners of di-ortho PCBs were noticed in the ranges of 1415-10325 and 663-7500 pg/ml respectively, in black and turkey vultures. Comparatively, greater toxic equivalency (TEQ) were observed in blood of turkey vultures with the ranges of 3.2-20, whereas black vulture contained 1.8-8.4 pgTEQ/ml wet wt. basis. The species-specific accumulation profiles of PCDD/DFs and dioxin-like PCBs may reflect the different feeding habits, ecology, metabolic capacity and migratory movements of these two scavenging species.

  17. Different behavioral effect dose–response profiles in mice exposed to two-carbon chlorinated hydrocarbons: Influence of structural and physical properties

    SciTech Connect

    Umezu, Toyoshi Shibata, Yasuyuki

    2014-09-01

    The present study aimed to clarify whether dose–response profiles of acute behavioral effects of 1,2-dichloroethane (DCE), 1,1,1-trichloroethane (TCE), trichloroethylene (TRIC), and tetrachloroethylene (PERC) differ. A test battery involving 6 behavioral endpoints was applied to evaluate the effects of DCE, TCE, TRIC, and PERC in male ICR strain mice under the same experimental conditions. The behavioral effect dose–response profiles of these compounds differed. Regression analysis was used to evaluate the relationship between the dose–response profiles and structural and physical properties of the compounds. Dose–response profile differences correlated significantly with differences in specific structural and physical properties. These results suggest that differences in specific structural and physical properties of DCE, TCE, TRIC, and PERC are responsible for differences in behavioral effects that lead to a variety of dose–response profiles. - Highlights: • We examine effects of 4 chlorinated hydrocarbons on 6 behavioral endpoints in mice. • The behavioral effect dose–response profiles for the 4 compounds are different. • We utilize regression analysis to clarify probable causes of the different profiles. • The compound's physicochemical properties probably produce the different profiles.

  18. An evaluation of the use of an advanced oxidation process to remove chlorinated hydrocarbons from groundwater at the US Department of Energy Kansas City Plant

    SciTech Connect

    Garland, S.B. II; Peyton, G.R.

    1990-10-01

    The Allied-Signal Aerospace Company currently operates a production facility in Kansas City, Missouri, under contract with the US Department of Energy (DOE). Over the years the operation of the DOE Kansas City Plant has resulted in the contamination of groundwater with chlorinated hydrocarbons, including trichloroethene (TCE). One of the plumes of contaminated groundwater, the underground tank farm (UTF) plume, was selected for remediation with an advanced oxidation process (AOP) consisting of simultaneous treatment by ozone (O{sub 3}), ultraviolet (UV) radiation, and hydrogen peroxide (H{sub 2}O{sub 2}). Since the use of AOPs is relatively new for the removal of organics from groundwater, information on design criteria, costs, performance, and operating experience is not well documented in the literature. Therefore, the Oak Ridge National Laboratory (ORNL) was requested to evaluate the treatment process. This report documents the work performed through FY 1989. The results of the initial year of the evaluations, FY 1988, have been published previously, and the evaluation will continue at least through FY 1990. This report first briefly describes the treatment plant and the mechanisms of the treatment process. Next, the methodology and the results from the evaluation are discussed. Finally, conclusions and recommendations are presented. 8 refs., 14 figs., 16 tabs.

  19. On-line analysis of volatile chlorinated hydrocarbons in air by gas chromatography-mass spectrometry Improvements in preconcentration and injection steps.

    PubMed

    Zoccolillo, Lelio; Amendola, Luca; Insogna, Susanna; Pastorini, Elisabetta

    2010-06-11

    An analytical system composed of a cryofocusing trap injector device coupled to a gas chromatograph with mass spectrometric detection (CTI-GC-MS) specific for the on-line analysis in air of volatile chlorinated hydrocarbons (VCHCs) (dichloromethane; chloroform; 1,1,1-trichloroethane; tetrachloromethane; 1,1,2-trichloroethylene; tetrachloroethylene) was developed. The cryofocusing trap injector was the result of appropriate low cost modifications to an original purge-and-trap device to make it suitable for direct air analysis even in the case of only slightly contaminated air samples, such as those from remote zones. The CTI device can rapidly and easily be rearranged into the purge-and-trap allowing water and air analysis with the same apparatus. Air samples, collected in stainless steel canisters, were introduced directly into the CTI-GC-MS system to realize cryo-concentration (at -120 degrees C), thermal desorption (at 200 degrees C) and for the subsequent analysis of volatiles. The operating phases and conditions were customised and optimized. Recovery efficiency was optimized in terms of moisture removal, cold trap temperature and sampling mass flow. The injection of entrapped volatiles was realized through a direct transfer with high chromatographic reliability (capillary column-capillary column). These improvements allowed obtaining limits of detection (LODs) at least one order of magnitude lower than current LODs for the investigated substances. The method was successfully employed on real samples: air from urban and rural areas and air from remote zones such as Antarctica.

  20. Estimating the in situ sediment-porewater distribution of PAHs and chlorinated aromatic hydrocarbons in anthropogenic impacted sediments

    SciTech Connect

    Hans Peter H. Arp; Gijs D. Breedveld; Gerard Cornelissen

    2009-08-15

    It has become increasingly apparent that the in situ sediment-porewater distribution behavior of organic compounds within anthropogenic impacted sediments is quite diverse, and challenging to generalize. Traditional models based on octanol-water partitioning generally overestimate native porewater concentrations, and modern approaches accounting for multiple carbon fractions, including black carbon, appear sediment specific. To assess the diversity of this sorption behavior, we collected all peer-reviewed total organic carbon (TOC)-normalized in situ sediment-porewater distribution coefficients, K{sub TOC}, for impacted sediments. This entailed several hundreds of data for PAHs, PCBs, PCDD/Fs, and chlorinated benzenes, covering a large variety of sediments, locations, and experimental methods. Compound-specific KTOC could range up to over 3 orders of magnitude. Output from various predictive models for individual carbonaceous phases found in impacted sediments, based on peer-reviewed polyparameter linear free energy relationships (PP-LFERs), Raoult's Law, and the SPARC online-calculator, were tested to see if any of the models could consistently predict literature K{sub TOC} values within a factor of 30 (i.e. about 1.5 orders of magnitude, or half the range of K{sub TOC} values). The Raoult's Law model and coal tar PP-LFER achieved the sought-after accuracy for all tested compound classes, and are recommended for general, regional-scale modeling purposes. As impacted sediment-porewater distribution models are unlikely to get more accurate than this, this review underpins that the only way to accurately obtain accurate porewater concentrations is to measure them directly, and not infer them from sediment concentrations. 86 refs., 2 figs., 3 tabs.

  1. Evaluation of solid polymeric organic materials for use in bioreactive sediment capping to stimulate the degradation of chlorinated aliphatic hydrocarbons.

    PubMed

    Atashgahi, Siavash; Maphosa, Farai; De Vrieze, Jo; Haest, Pieter Jan; Boon, Nico; Smidt, Hauke; Springael, Dirk; Dejonghe, Winnie

    2014-03-01

    In situ bioreactive capping is a promising technology for mitigation of surface water contamination by discharging polluted groundwater. Organohalide respiration (OHR) of chlorinated ethenes in bioreactive caps can be stimulated through incorporation of solid polymeric organic materials (SPOMs) that provide a sustainable electron source for organohalide respiring bacteria. In this study, wood chips, hay, straw, tree bark and shrimp waste, were assessed for their long term applicability as an electron donor for OHR of cis-dichloroethene (cDCE) and vinyl chloride (VC) in sediment microcosms. The initial release of fermentation products, such as acetate, propionate and butyrate led to the onset of extensive methane production especially in microcosms amended with shrimp waste, straw and hay, while no considerable stimulation of VC dechlorination was obtained in any of the SPOM amended microcosms. However, in the longer term, short chain fatty acids accumulation decreased as well as methanogenesis, whereas high dechlorination rates of VC and cDCE were established with concomitant increase of Dehalococcoides mccartyi and vcrA and bvcA gene numbers both in the sediment and on the SPOMs. A numeric simulation indicated that a capping layer of 40 cm with hay, straw, tree bark or shrimp waste is suffice to reduce the groundwater VC concentration below the threshold level of 5 μg/l before discharging into the Zenne River, Belgium. Of all SPOMs, the persistent colonization of tree bark by D. mccartyi combined with the lowest stimulation of methanogenesis singled out tree bark as a long-term electron donor for OHR of cDCE/VC in bioreactive caps.

  2. Aqueous chlorination of resorcinol

    USGS Publications Warehouse

    Heasley, V.L.; Burns, M.D.; Kemalyan, N.A.; Mckee, T.C.; Schroeter, H.; Teegarden, B.R.; Whitney, S.E.; Wershaw, R. L.

    1989-01-01

    An investigation of the aqueous chlorination (NaOCl) of resorcinol is reported. The following intermediates were detected in moderate to high yield at different pH values and varying percentages of chlorination: 2-chloro-, 4-chloro-, 2,4-dichloro-, 4,6-dichloro- and 2,4,6-trichlororesorcinol. Only trace amounts of the intermediates were detected when the chlorination was conducted in the presence of phosphate buffer. This result has significant implications since resorcinol in phosphate buffer has been used as a model compound in several recent studies on the formation of chlorinated hydrocarbons during chlorination of drinking water. Relative rates of chlorination were determined for resorcinol and several of the chlorinated resorcinols. Resorcinol was found to chlorinate only three times faster than 2,4,6-trichlororesorcinol. The structure 2,4,6-trichlororesorcinol was established as a monohydrate even after sublimation. A tetrachloro or pentachloro intermediate was not detected, suggesting that the ring-opening step of such an intermediate must be rapid. ?? 1989.

  3. Mobilization of soil bound residue of organochlorine pesticides and polycyclic aromatic hydrocarbons in an in-vitro gastrointestinal model

    PubMed Central

    TAO, SHU; LI, LI; DING, JUNNAN; ZHONG, JUNJUN; ZHANG, DIYU; LU, YAN; YANG, YIFENG; WANG, XILONG; LI, XIQING; CAO, JUN; LU, XIAOXIA; LIU, WENXIN

    2011-01-01

    A previous study on mobilization of organochlorine pesticides (OCPs) in contaminated soils from the field revealed that the total amount of OCPs measured in digestive fluid and chyme of an in-vitro gastrointestinal model was higher than the quantity directly extracted using a solvent extraction without digestion, providing a clue that the bound residue of OCPs might be mobilized. This hypothesis was tested in this study for both OCPs and polycyclic aromatic hydrocarbons (PAHs). Three contaminated surface soil samples with different organic carbon (OC) contents were collected from the field, and extracted with a solvent with and without digestion in an in-vitro gastrointestinal model. It was found that bound residues of OCPs and PAHs were mobilized to a certain extent during digestion. The ratios of the mobilized bound residues over the total quantities extracted after digestion (Rb) varied from 0 to 0.96 for individual compounds. The Rb was positively correlated with OC content. Among the five constitutes of digestive juice, bile salt was the only one that served to mobilize the bound residues and the extractability of bile salt was constant over a concentration range from 2 to 20 mg/mL. The mobilization process followed typical first-order kinetics. The calculated rate constants suggest that mobilization was fast and 90% of extracted bound residues of OCPs and PAHs were mobilized within 2.4 and 4.8 h, respectively. PMID:21175124

  4. Chlorinated hydrocarbons and biomarkers of exposure in wading birds and fish of the Lower Rio Grande Valley, Texas

    USGS Publications Warehouse

    Wainwright, S.E.; Mora, M.A.; Sericano, J.L.; Thomas, P.

    2001-01-01

    During 1997 we evaluated reproductive success in colonial water birds nesting in the Lower Rio Grande Valley (LRGV), Texas, and correlated success with concentrations of contaminants in eggs. We also measured steroid hormones and gonadosomatic index (GSI) as biomarkers of endocrine effects in common carp (Cyprinus carpio). Nest and fledging success of green herons (Butorides virescens) and great egrets (Ardea alba) were similar to those found in other parts of North America; however, nesting success of black-crowned night-herons (Nycticorax nycticorax) was lower, very likely due to flooding of the nesting area. Except for DDE and toxaphene, all chlorinated pesticides in bird eggs were low and not of concern for negative effects on any of the three species. DDE was highest in green heron eggs and seemed to increase along a geographic gradient from west to east, with eggs from Falcon Reservoir containing low concentrations, and those at Los Indios containing the highest concentrations (approx. 11,000 ng/g WW), near or above the threshold for reproductive impairment. DDE levels in great egrets and black-crowned night-herons were below those that are associated with reproductive impairment. Mean DDE levels in carp at the JAS Farms site were above the threshold level suggested for predator protection. Toxaphene was detected in about 20% of the samples with high levels observed in green heron eggs from Los Indios (mean = 4,402 ng/g WW). These are the highest toxaphene levels reported in bird eggs in the LRGV. Toxaphene levels in fish ranged between 90 and 312 ng/g WW. In general, PCBs in bird eggs and fish tissue were low and at levels not of concern for reproductive effects. The greatest concentrations of testosterone and 11-ketotestosterone were detected in fish from the JAS Farms site, which also had the greatest concentrations of DDE. Increased androgen production and gonad development in fish at this site, relative to Pharr, could be possibly associated with

  5. Chlorinated and parent polycyclic aromatic hydrocarbons in environmental samples from an electronic waste recycling facility and a chemical industrial complex in China.

    PubMed

    Ma, Jing; Horii, Yuichi; Cheng, Jinping; Wang, Wenhua; Wu, Qian; Ohura, Takeshi; Kannan, Kurunthachalam

    2009-02-01

    Chlorinated polycyclic aromatic hydrocarbons (CIPAHs) are a class of halogenated contaminants found in the urban atmosphere; they have toxic potential similar to that of dioxins. Information on the sources of CIPAHs is limited. In this study, concentrations of 20 CIPAHs and 16 parent PAHs were measured in electronic wastes, workshop-floor dust, vegetation, and surface soil collected from the vicinity of an electronic waste (e-waste) recycling facility and in surface soil from a chemical industrial complex (comprising a coke-oven plant, a coal-fired power plant, and a chlor-alkali plant), and agricultural areas in central and eastern China. High concentrations of SigmaCIPAHs were found in floor dust (mean, 103 ng/g dry wt), followed in order of decreasing concentration by leaves (87.5 ng/g drywt), electronic shredder waste (59.1 ng/g dry wt), and soil (26.8 ng/g dry wt) from an e-waste recycling facility in Taizhou. The mean concentration of SigmaCIPAHs in soil from the chemical industrial complex (88 ng/g dry wt) was approximately 3-fold higher than the concentration in soil from e-waste recycling facilities. The soils from e-waste sites and industrial areas contained mean concentrations of SigmaCIPAHs 2 to 3 orders of magnitude higher than the concentrations in agricultural soils (ND-0.76 ng/g), suggesting that e-waste recycling and chlorine-chemical industries are potential emission sources of CIPAHs. The profiles of CIPAHs in soil and dust were similar to a profile that has been reported previously for fly ash from municipal solid waste incinerators (6-CIBaP was the predominant compound), but the profiles in vegetation and electronic shredder waste were different from those found in fly ash. Concentrations of 16 parent PAHs were high (150-49,700 ng/g) in samples collected from the e-waste recycling facility. Significant correlation between SigmaCIPAH and SigmaPAH concentrations suggests that direct chlorination of parent PAHs is the major pathway of formation of

  6. Hepatic microsomal cytochrome p450s and chlorinated hydrocarbons in largha and ribbon seals from Hokkaido, Japan: differential response of seal species to Ah receptor agonist exposure.

    PubMed

    Chiba, Issei; Sakakibara, Akihito; Iwata, T Hisato; Ishizuka, Mayumi; Tanabe, Shinsuke; Akahori, Fumiaki; Kazusaka, Akio; Fujita, Shoichi

    2002-04-01

    From 16 largha seals (Phoca largha) and 15 ribbon seals (Phoca fasciata) in the coastal waters of Hokkaido, Japan, blubber chlorinated hydrocarbon (CHC) levels and hepatic cytochrome P450 (CYP) catalytic activities and their immunochemically detected protein content levels were measured. Concentrations of DDTs (2,2-bis(4-chlorophenyl)-1,1-dichloroethylene,p,p'-DDE; 2,2-bis(4-chlorophenyl)-1,1-dichloroethane, p,p'-DDD; dichlorodiphenyltrichloroethane, p,p'-DDT), polychlorinated biphenyl congeners (PCBs), and chlordane compounds (oxychlordane, chlordanes, and nonachlors) in both species were in the range of 290 to 5,300, 420 to 4,000, and 130 to 1,500 ng/g lipid weight, respectively. Aryl hydrocarbon receptor (AhR) agonists, non-ortho (IUPAC 77 and 126) and mono-ortho (IUPAC 105, 118, and 156) coplanar PCB congeners, were also detected, and the 2,3,7,8-tetrachlordibenzo-p-dioxin (TCDD) toxic equivalents (TEQs) were 4.9 to 120 pg TEQ/g lipid weight. Cross-reactive proteins with polyclonal antibodies against rat CYP1A1 and CYP3A2 were notably detected in seal liver microsomes. Interestingly, a polyclonal antibody against rat CYP2B1 recognized proteins only at trace levels. In largha seals, both levels of alkoxyresorufin- (methoxy-, ethoxy-, pentoxy-, and benzyloxyresorufin) O-dealkylase (AROD) activities and proteins detected by polyclonal antibodies against rat CYP1A1 were significantly correlated with the concentrations of individual coplanar PCB congeners, total TEQs, and total PCBs. Threshold concentrations for TEQs in blubber of the largha seal to induce hepatic CYP1A protein and EROD activity were estimated to be 8.5 and 19 pg TEQ/g fat weight, respectively. In ribbon seals, similar correlations were not detected, although the TEQ levels were not significantly lower than those in largha seals. These results suggest that AROD activity and CYP1A1 protein in the liver of the largha seal could be a biomarker for the exposure to AhR agonists such as coplanar PCB

  7. Behaviour of I/Br/Cl-THMs and their projected toxicities under simulated cooking conditions: Effects of heating, table salt and residual chlorine.

    PubMed

    Yan, Mingquan; Li, Mingyang; Han, Xuze

    2016-08-15

    This study examined the effects of heating, residual chlorine and concentration of table salt on the generation of iodine-, bromine- and chlorine-containing trihalomethanes (THMs) under simulated cooking conditions. In the case of addition of either KI- or KIO3-fortified salt, total I-THM concentrations increased with increasing iodine concentration, while total Cl/Br-THM concentrations decreased. CHCl2I, CHBrClI, CHBrI2, CHBr2I and CHI3 were formed in the presence of KI salt, while only CHCl2I was formed in the presence of KIO3 salt. CHCl2I was unstable under cooking conditions, and >90% of this DBP was removed during heating, which in some cases increased the concentrations of the other I-THMs. The calculated cytotoxicity increased with addition of KI- or KIO3-fortified salt due to the generation of I-THMs, whose impact on the cytotoxicity at room temperature was equal to or five times higher, respectively, than the cytotoxicity of the simultaneously formed Cl/Br-THMs for the cases of salts. Heating decreased the cytotoxicity, except for the case of addition of KI salt, in which the calculated cytotoxicity of I-THMs increased above 150% as the temperature was increased up to 100°C. The reported results may have important implications for epidemiologic exposure assessments and, ultimately, for public health protection. PMID:27107240

  8. Behaviour of I/Br/Cl-THMs and their projected toxicities under simulated cooking conditions: Effects of heating, table salt and residual chlorine.

    PubMed

    Yan, Mingquan; Li, Mingyang; Han, Xuze

    2016-08-15

    This study examined the effects of heating, residual chlorine and concentration of table salt on the generation of iodine-, bromine- and chlorine-containing trihalomethanes (THMs) under simulated cooking conditions. In the case of addition of either KI- or KIO3-fortified salt, total I-THM concentrations increased with increasing iodine concentration, while total Cl/Br-THM concentrations decreased. CHCl2I, CHBrClI, CHBrI2, CHBr2I and CHI3 were formed in the presence of KI salt, while only CHCl2I was formed in the presence of KIO3 salt. CHCl2I was unstable under cooking conditions, and >90% of this DBP was removed during heating, which in some cases increased the concentrations of the other I-THMs. The calculated cytotoxicity increased with addition of KI- or KIO3-fortified salt due to the generation of I-THMs, whose impact on the cytotoxicity at room temperature was equal to or five times higher, respectively, than the cytotoxicity of the simultaneously formed Cl/Br-THMs for the cases of salts. Heating decreased the cytotoxicity, except for the case of addition of KI salt, in which the calculated cytotoxicity of I-THMs increased above 150% as the temperature was increased up to 100°C. The reported results may have important implications for epidemiologic exposure assessments and, ultimately, for public health protection.

  9. Use of mussels and semipermeable membrane devices to assess bioavailability of residual polynuclear aromatic hydrocarbons three years after the Exxon Valdez oil spill

    SciTech Connect

    Shigenaka, G.; Henry, C.B. Jr.

    1995-12-31

    Mussels (Mytilus cf. trossulus) were transplanted to a heavily oiled and extensively treated site on Smith Island, Prince William Sound, Alaska, in 1992. A new monitoring and assessment tool, the semipermeable membrane device, was also deployed to compare hydrocarbon uptake with mussels and to evaluate the route of exposure to mussels. Both mussels and semipermeable membrane devices accumulated polynuclear aromatic hydrocarbons during 14- and 52-day deployments, particularly at the oiled site. Accumulation levels were similar between mussels and the semipermeable membrane devices, but the distribution of individual hydrocarbons differed. The results permit some inference about route of exposure to mussels. Sheens leaching from subsurface deposits of residual oil, and particulate material with adsorbed hydrocarbons were apparently more important exposure pathways than dissolved hydrocarbons in water. Semipermeable membrane devices show promise as monitoring tools and to provide insights into exposure pathways for biota. 20 refs., 7 figs., 4 tabs.

  10. [Hydrocarbons and chlorinated hydrocarbons in groundwater].

    PubMed

    Hanert, H H

    1989-01-01

    The contribution deals with the following topics: --Microbiological in situ investigations of polluted ground water aquifers in order to develop a concept for biological remediation. --Removal of organic and halogenated organic compounds from ground water using methods which are common in the drinking water treatment (sand-fastfiltering, immobilized reactors). --Removal of organic and halogenated organic compounds from ground water using methods which are common in sewage treatment (activated sludge, suspension reactors). The conclusion has been drawn that there are many microbiological methods existing which can be used to remove the above contaminants from soil and ground water environments.

  11. Remediation of inorganic contaminants and polycyclic aromatic hydrocarbons from soils polluted by municipal solid waste incineration residues.

    PubMed

    Jobin, Philippe; Coudert, Lucie; Taillard, Vincent; Blais, Jean-Francois; Mercier, Guy

    2016-08-01

    Three soils polluted by municipal solid waste (MSW) incineration residues and containing various concentrations of Cu, Pb, Sb, Sn and Zn were treated using magnetism, gravity separation (jig and shaking table) and flotation/leaching. The process removed between 18% and 39% of the contaminants present in soil 1, between 31% and 53% of the contaminants present in soil 2 and between 42% and 56% of the contaminants present in soil 3. Polycyclic aromatic hydrocarbons were present only in soil 3, and the process removed 64% of its PAHs total content. Magnetism seemed to be the most efficient technique to remove metals from contaminated soils, followed by gravity separation and finally flotation/leaching. The global efficiency of the process was higher when the initial contaminant concentrations were lower (smaller proportions of MSW incineration residues). The estimated costs of the process, including direct and indirect costs, varied from $82 to $88 per ton of treated soil depending on the proportion of MSW incineration residues mixed with the soil.

  12. Remediation of inorganic contaminants and polycyclic aromatic hydrocarbons from soils polluted by municipal solid waste incineration residues.

    PubMed

    Jobin, Philippe; Coudert, Lucie; Taillard, Vincent; Blais, Jean-Francois; Mercier, Guy

    2016-08-01

    Three soils polluted by municipal solid waste (MSW) incineration residues and containing various concentrations of Cu, Pb, Sb, Sn and Zn were treated using magnetism, gravity separation (jig and shaking table) and flotation/leaching. The process removed between 18% and 39% of the contaminants present in soil 1, between 31% and 53% of the contaminants present in soil 2 and between 42% and 56% of the contaminants present in soil 3. Polycyclic aromatic hydrocarbons were present only in soil 3, and the process removed 64% of its PAHs total content. Magnetism seemed to be the most efficient technique to remove metals from contaminated soils, followed by gravity separation and finally flotation/leaching. The global efficiency of the process was higher when the initial contaminant concentrations were lower (smaller proportions of MSW incineration residues). The estimated costs of the process, including direct and indirect costs, varied from $82 to $88 per ton of treated soil depending on the proportion of MSW incineration residues mixed with the soil. PMID:26729603

  13. Role of Hot Water System Design on Factors Influential to Pathogen Regrowth: Temperature, Chlorine Residual, Hydrogen Evolution, and Sediment

    PubMed Central

    Brazeau, Randi H.; Edwards, Marc A.

    2013-01-01

    Abstract Residential water heating is linked to growth of pathogens in premise plumbing, which is the primary source of waterborne disease in the United States. Temperature and disinfectant residual are critical factors controlling increased concentration of pathogens, but understanding of how each factor varies in different water heater configurations is lacking. A direct comparative study of electric water heater systems was conducted to evaluate temporal variations in temperature and water quality parameters including dissolved oxygen levels, hydrogen evolution, total and soluble metal concentrations, and disinfectant decay. Recirculation tanks had much greater volumes of water at temperature ranges with potential for increased pathogen growth when set at 49°C compared with standard tank systems without recirculation. In contrast, when set at the higher end of acceptable ranges (i.e., 60°C), this relationship was reversed and recirculation systems had less volume of water at risk for pathogen growth compared with conventional systems. Recirculation tanks also tended to have much lower levels of disinfectant residual (standard systems had 40–600% higher residual), 4–6 times as much hydrogen, and 3–20 times more sediment compared with standard tanks without recirculation. On demand tankless systems had very small volumes of water at risk and relatively high levels of disinfectant residual. Recirculation systems may have distinct advantages in controlling pathogens via thermal disinfection if set at 60°C, but these systems have lower levels of disinfectant residual and greater volumes at risk if set at lower temperatures. PMID:24170969

  14. Reaction products of chlorine dioxide.

    PubMed Central

    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 dioxide treatment of organic materials are oxidized species, some of which also contain chlorine. The relative amounts of species types may depend on the amount of chlorine dioxide residual maintained and the concentration and nature of the organic material present in the source water. The trend toward lower concentrations of chlorinated by-products with increasing ClO2 concentration, which was observed with phenols, has not been observed with natural humic materials as measured by the organic halogen parameter. Organic halogen concentrations have been shown to increase with increasing chlorine dioxide dose, but are much lower than those observed when chlorine is applied. Aldehydes have been detected as apparent by-products of chlorine dioxide oxidation reactions in a surface water that is a drinking water source. Some other nonchlorinated products of chlorine dioxide treatment may be quinones and epoxides. The extent of formation of these moieties within the macromolecular humic structure is also still unknown. PMID:7151750

  15. Simultaneous determination of polycyclic aromatic hydrocarbons and their chlorination by-products in drinking water and the coatings of water pipes by automated solid-phase microextraction followed by gas chromatography-mass spectrometry.

    PubMed

    Tillner, Jocelyn; Hollard, Caroline; Bach, Cristina; Rosin, Christophe; Munoz, Jean-François; Dauchy, Xavier

    2013-11-01

    In this study, an automated method for the simultaneous determination of polycyclic aromatic hydrocarbons (PAHs) and their chlorination by-products in drinking water was developed based on online solid-phase microextraction-gas chromatography-mass spectrometry. The main focus was the optimisation of the solid-phase microextraction step. The influence of the agitation rate, type of fibre, desorption time, extraction time, extraction temperature, desorption temperature, and solvent addition was examined. The method was developed and validated using a mixture of 17 PAHs, 11 potential chlorination by-products (chlorinated and oxidised PAHs) and 6 deuterated standards. The limit of quantification was 10 ng/L for all target compounds. The validated method was used to analyse drinking water samples from three different drinking water distribution networks and the presumably coal tar-based pipe coatings of two pipe sections. A number of PAHs were detected in all three networks although individual compositions varied. Several PAH chlorination by-products (anthraquinone, fluorenone, cyclopenta[d,e,f]phenanthrenone, 3-chlorofluoranthene, and 1-chloropyrene) were also found, their presence correlating closely with that of their respective parent compounds. Their concentrations were always below 100 ng/L. In the coatings, all PAHs targeted were detected although concentrations varied between the two coatings (76-12,635 mg/kg and 12-6295 mg/kg, respectively). A number of chlorination by-products (anthraquinone, fluorenone, cyclopenta[d,e,f]phenanthrenone, 3-chlorofluoranthene, and 1-chloropyrene) were also detected (from 40 to 985 mg/kg), suggesting that the reaction of PAHs with disinfectant agents takes place in the coatings and not in the water phase after migration.

  16. Inactivation of influenza virus haemagglutinin by chlorine dioxide: oxidation of the conserved tryptophan 153 residue in the receptor-binding site.

    PubMed

    Ogata, Norio

    2012-12-01

    Airborne influenza virus infection of mice can be prevented by gaseous chlorine dioxide (ClO(2)). This study demonstrated that ClO(2) abolished the function of the haemagglutinin (HA) of influenza A virus (H1N1) in a concentration-, time- and temperature-dependent manner. The IC(50) during a 2 min reaction with ClO(2) at 25 °C was 13.7 µM, and the half-life time of HA with 100 µM ClO(2) at 25 °C was 19.5 s. Peptides generated from a tryptic digest of ClO(2)-treated virus were analysed by mass spectrometry. An HA fragment, (150)NLLWLTGK(157) was identified in which the tryptophan residue (W153) was 32 mass units greater than expected. The W153 residue of this peptide, which is derived from the central region of the receptor-binding site of HA, is highly conserved. It was shown that W153 was oxidized to N-formylkynurenine in ClO(2)-treated virus. It was concluded that the inactivation of influenza virus by ClO(2) is caused by oxidation of W153 in HA, thereby abolishing its receptor-binding ability.

  17. Study of weathering effects on the distribution of aromatic steroid hydrocarbons in crude oils and oil residues.

    PubMed

    Wang, Chuanyuan; Chen, Bing; Zhang, Baiyu; Guo, Ping; Zhao, Mingming

    2014-01-01

    The composition and distribution of triaromatic steroid hydrocarbons in oil residues after biodegradation and photo-oxidation processes were detected, and the diagnostic ratios for oil spill identification were developed and evaluated based on the relative standard deviation (RSD) and the repeatability limit. The preferential loss of C27 methyl triaromatic steranes (MTAS) relative to C28 MTAS and C29 MTAS was shown during the photo-oxidation process. In contrast to the photochemical degradation, the MTAS with the original 20R biological configuration was preferentially degraded during the biodegradation process. The RSD of most of the diagnostic ratios of MTAS ranged from 9 to 84% during the photo-oxidation process. However, the RSDs of such ratios derived from MTAS were all <5% even in high biodegradation, and such parameters may also provide new methods on oil spill identification. The parameters of monoaromatic sterane and monoaromatic sterane are not used well for oil spill identification after photo-oxidation. The triaromatic steroid hydrocarbons retained their molecular compositions after biodegradation and photo-oxidation and most of the diagnostic ratios derived from them could be efficiently used in oil spill identification.

  18. Study of weathering effects on the distribution of aromatic steroid hydrocarbons in crude oils and oil residues.

    PubMed

    Wang, Chuanyuan; Chen, Bing; Zhang, Baiyu; Guo, Ping; Zhao, Mingming

    2014-01-01

    The composition and distribution of triaromatic steroid hydrocarbons in oil residues after biodegradation and photo-oxidation processes were detected, and the diagnostic ratios for oil spill identification were developed and evaluated based on the relative standard deviation (RSD) and the repeatability limit. The preferential loss of C27 methyl triaromatic steranes (MTAS) relative to C28 MTAS and C29 MTAS was shown during the photo-oxidation process. In contrast to the photochemical degradation, the MTAS with the original 20R biological configuration was preferentially degraded during the biodegradation process. The RSD of most of the diagnostic ratios of MTAS ranged from 9 to 84% during the photo-oxidation process. However, the RSDs of such ratios derived from MTAS were all <5% even in high biodegradation, and such parameters may also provide new methods on oil spill identification. The parameters of monoaromatic sterane and monoaromatic sterane are not used well for oil spill identification after photo-oxidation. The triaromatic steroid hydrocarbons retained their molecular compositions after biodegradation and photo-oxidation and most of the diagnostic ratios derived from them could be efficiently used in oil spill identification. PMID:25144907

  19. Chlorine demand of Savannah River water

    SciTech Connect

    Wilde, E.W.

    1989-01-01

    Savannah River water used for cooling SRS reactors was tested for chlorine demand and the rate of decay for both free and total residual chlorine on seven quarterly dates between 1986 and 1988. Test conditions included chlorine dosages of 1, 3, and 5 mg/l and a variety of contact times ranging from less than 1 minute to one day. Statistically significant differences were detected in the chlorine demand for the seven dates; however, there was no discernible seasonality to the variation. The chlorine demand, amount of combined residual chlorine formed and the persistence of total residual chlorine following a dose of 5 mg/l was significantly greater on one of the seven sampling dates (February, 1988) compared to all of the other dates. These differences could not be attributed to water temperature, pH, ammonia nitrogen concentration, or the amount of rainfall prior to or during the collection of the cooling water. Except as noted above, dissipation of chlorine was similar among the sampling dates. Most reactions of available chlorine with other constituents in the cooking water occurred in the first minute of contact, although measurable total chlorine residuals generally persisted for 24 hours after the dose had been administered. The results of this study indicate that, with occasional exceptions, a chlorine dose of between 3 and 5 mg/l will provide a free chlorine residual of 1 mg/l in Savannah River water. 14 refs., 3 figs., 4 tabs.

  20. Multi-class, multi-residue analysis of pesticides, polychlorinated biphenyls, polycyclic aromatic hydrocarbons, polybrominated diphenyl ethers and novel flame retardants....mass spectrometry

    Technology Transfer Automated Retrieval System (TEKTRAN)

    A multi-class, multi-residue method for the analysis of 13 novel flame retardants, 18 representative pesticides, 14 polychlorinated biphenyl (PCB) congeners, 16 polycyclic aromatic hydrocarbons (PAHs), and 7 polybrominated diphenyl ether (PBDE) congeners in catfish muscle was developed and evaluated...

  1. Direct immersion-solid phase microextraction for the determination of chlorinated pesticide residues in tomatoes by gas chromatography with an electron capture detector.

    PubMed

    Mariani, Maurizio Boccacci; Giannetti, Vanessa; Testani, Elena; Ceccarelli, Valentina

    2013-01-01

    The use of pesticides in agriculture has grown dramatically over the last decades. Environmental exposure of humans to agrochemicals is common and results in both acute and chronic health effects. In this study, direct immersion-solid phase microextraction (SPME) was coupled with electron capture detection for trace determination of 19 chlorinated pesticides in tomato samples, using a 100 pm polydimethylsiloxane fiber. The experimental parameters extraction time, extraction temperature, stirring, and salting out were evaluated and optimized. The LODs ranged from 0.5 to 8 microg/kg, and the LOQs from 5 to 30 microg/kg. A linear response was confirmed by correlation coefficients ranging from 0.97 to 0.9985. The developed method was tested by analyzing real samples purchased within the network of Italian distribution. The samples were found to be free from detectable residues of the studied pesticides. SPME has been shown to be a fast extraction technique that has several advantages such as solvent-free extraction, simplicity, and compatibility with the chromatographic analytical system. PMID:24645525

  2. Petroleum hydrocarbon residues in the marine environment of Bassein-Mumbai.

    PubMed

    Chouksey, Mithlesh Kumar; Kadam, A N; Zingde, M D

    2004-10-01

    The paper reports PHc contamination in water, sediment and biota of the coastal area of Bassein-Mumbai in relation to relatively less polluted sites (Dabhol and Ratnagiri) off the west coast of India. To facilitate inter-comparison three standards have been used though the results are reported in terms of SAM (Residue of Saudi Arabian Mix crude). The concentration of PHc in water off Bassein-Mumbai varies widely (2.9-39.2 microg l(-1)) as compared to the average baseline (2.8 microg l(-1)) with higher values generally confined to creeks and estuaries. The higher concentration of PHc in the bottom water of shallow areas is attributed to the contribution from the sediment-associated petroleum residue. High concentration of PHc in the surficial sediment of inshore area Ratnagiri (107.7 ppm, dry wt) is perhaps the remnants of an oil spill that occurred in the Bombay High region on May 17, 1993. The majority of values of PHc concentration in the surficial sediment of the Bassein-Mumbai region exceed 15 ppm (dry wt) against the expected background (<3 ppm, dry wt) and the trend is indicative of transfer of PHc loads from the inshore areas to the open-shore sediments. The PHc concentration of 0.8-2.6 ppm (dry wt) in sediment deposited prior to the first global commercial use of petroleum in core R5 represents the biogenic background. Based on the period of industrialisation and the horizon of PHc accumulation, a sedimentation rate of 0.2 and 1.0 cm y(-1) respectively is estimated for cores U11 and U12. Substantial increase in the concentration of PHc in sediment after 1950 in cores T8 and T10 correlates well with the establishment of refineries on the western shore of the Thane Creek in 1955-1960. A minor peak in most cores in the top 10 cm sediment probably results from biological transfer of PHc lower into the sediment by benthic organisms. Excess of PHc retained in the sediment of the Bassein-Mumbai region over the biogenic background is estimated at 40,000 t. The PHc

  3. Degradation of polycyclic aromatic hydrocarbons in a coking wastewater treatment plant residual by an O3/ultraviolet fluidized bed reactor.

    PubMed

    Lin, Chong; Zhang, Wanhui; Yuan, Mengyang; Feng, Chunhua; Ren, Yuan; Wei, Chaohai

    2014-09-01

    Coking wastewater treatment plant (CWWTP) represents a typical point source of polycyclic aromatic hydrocarbons (PAHs) to the water environment and threatens the safety of drinking water in downstream regions. To enhance the removal of residual PAHs from bio-treated coking wastewater, a pilot-scale O3/ultraviolet (UV) fluidized bed reactor (O3/UV FBR) was designed and different operating factors including UV irradiation intensity, pH, initial concentration, contact time, and hydraulic retention time (HRT) were investigated at an ozone level of 240 g h(-1) and 25 ± 3 °C. A health risk evaluation and cost analysis were also carried out under the continuous-flow mode. As far as we know, this is the first time an O3/UV FBR has been explored for PAHs treatment. The results indicated that between 41 and 75 % of 18 target PAHs were removed in O3/UV FBR due to synergistic effects of UV irradiation. Both increased reaction time and increased pH were beneficial for the removal of PAHs. The degradation of the target PAHs within 8 h can be well fitted by the pseudo-first-order kinetics (R (2) > 0.920). The reaction rate was also positively correlated with the initial concentrations of PAHs. The health risk assessment showed that the total amount of carcinogenic substance exposure to surface water was reduced by 0.432 g day(-1). The economic analysis showed that the O3/UV FBR was able to remove 18 target PAHs at a cost of US$0.34 m(-3). These results suggest that O3/UV FBR is efficient in removing residuals from CWWTP, thus reducing the accumulation of persistent pollutant released to surface water.

  4. Studies of the movement and the formation of bound residues of atrazine, of its chlorinated derivatives, and of hydroxyatrazine in soil using /sup 14/C ring-labeled compounds under outdoor conditions

    SciTech Connect

    Schiavon, M.

    1988-02-01

    Using unperturbed-structure soil columns, placed under field conditions for a 1-year period, we have evaluated the possibilities of penetration into the soil of various /sup 14/C ring-labeled s-triazinic compounds: atrazine, chlorinated derivatives, and hydroxyatrazine. We have simultaneously examined the possibilities of formation of bound residues for each of the compounds. 2-Cl-4,6-Diaminoatrazine appears to be the product most apt to form bound residues but this reaction is paralleled by a rapid loss of total residues. On the other hand, hydroxyatrazine is a strongly adsorbed product which is lost from the soil into the atmosphere only slowly and forms practically no bound residues.

  5. Two years after the Hebei Spirit oil spill: residual crude-derived hydrocarbons and potential AhR-mediated activities in coastal sediments.

    PubMed

    Hong, Seongjin; Khim, Jong Seong; Ryu, Jongseong; Park, Jinsoon; Song, Sung Joon; Kwon, Bong-Oh; Choi, Kyungho; Ji, Kyunghee; Seo, Jihyun; Lee, Sangwoo; Park, Jeongim; Lee, Woojin; Choi, Yeyong; Lee, Kyu Tae; Kim, Chan-Kook; Shim, Won Joon; Naile, Jonathan E; Giesy, John P

    2012-02-01

    The Hebei Spirit oil spill occurred in December 2007 approximately 10 km off the coast of Taean, South Korea, on the Yellow Sea. However, the exposure and potential effects remain largely unknown. A total of 50 surface and subsurface sediment samples were collected from 22 sampling locations at the spill site in order to determine the concentration, distribution, composition of residual crudes, and to evaluate the potential ecological risk after two years of oil exposure. Samples were extracted and analyzed for 16 polycyclic aromatic hydrocarbons (PAHs), 20 alkyl-PAHs, 15 aliphatic hydrocarbons, and total petroleum hydrocarbons using GC-MSD. AhR-mediated activity associated with organic sediment extracts was screened using the H4IIE-luc cell bioassay. The response of the benthic invertebrate community was assessed by mapping the macrobenthic fauna. Elevated concentrations of residual crudes from the oil spill were primarily found in muddy bottoms, particularly in subsurface layers. In general, the bioassay results were consistent with the chemistry data in a dose-dependent manner, although the mass-balance was incomplete. More weathered samples containing greater fractions of alkylated PAHs exhibited greater AhR activity, due to the occurrence of recalcitrant AhR agonists present in residual oils. The macrobenthic population distribution exhibits signs of species-specific tolerances and/or recolonization of certain species such as Batillaria during weathering periods. Although the Hebei Spirit oil spill was a severe oil exposure, it appears the site is recovering two years later.

  6. Review of chlorinated phenols

    SciTech Connect

    Exon, J.H.

    1984-12-01

    The chlorinated phenols are a group of 19 isomers composed of phenol with substituted chlorines. These chemicals are readily soluble in organic solvents but only slightly soluble in water, except for the chlorophenate salts. Chlorophenols with less than 3 chlorines are not used extensively except in the production of higher chlorophenols and chlorophenyloxyacetic acid herbicides. Pentachlorophenol and some tetrachlorophenols are used worldwide, primarily as wood preservatives or fungicides. Residues of chlorophenols have been found worldwide in soil, water and air samples, in food products, and in human and animal tissues and body fluids. Environmental contamination with these chemicals occurs from industrial effluents, agricultural runoff, breakdown of chlorophenyloxyacetic acid herbicides and hexachlorobenzene, and from spontaneous formation following chlorination of water for disinfection and deodorization. The acute toxicity of these chemicals is relatively low and little is known concerning their chronic effects. Chlorophenols have not been shown conclusively to be mutagens, teratogens or carcinogens. However, these compounds may act as promotors or cocarcinogens and the immune system is particularly sensitive to their toxic effects. Transplacental exposure to chlorophenols may result in embryotoxicity and abortion. The major mode of toxic action is as uncouplers of oxidative phosphorylation. The toxicity of chlorophenols decreases with decreasing chlorination. These chemicals are mild hepatotoxins and are stored mainly in hepatic and renal tissues.

  7. Characterization of Preferential Ground-Water Seepage From a Chlorinated Hydrocarbon-Contaminated Aquifer to West Branch Canal Creek, Aberdeen Proving Ground, Maryland, 2002-04

    USGS Publications Warehouse

    Majcher, Emily H.; Phelan, Daniel J.; Lorah, Michelle M.; McGinty, Angela L.

    2007-01-01

    Wetlands act as natural transition zones between ground water and surface water, characterized by the complex interdependency of hydrology, chemical and physical properties, and biotic effects. Although field and laboratory demonstrations have shown efficient natural attenuation processes in the non-seep wetland areas and stream bottom sediments of West Branch Canal Creek, chlorinated volatile organic compounds are present in a freshwater tidal creek at Aberdeen Proving Ground, Maryland. Volatile organic compound concentrations in surface water indicate that in some areas of the wetland, preferential flow paths or seeps allow transport of organic compounds from the contaminated sand aquifer to the overlying surface water without undergoing natural attenuation. From 2002 through 2004, the U.S. Geological Survey, in cooperation with the Environmental Conservation and Restoration Division of the U.S. Army Garrison, Aberdeen Proving Ground, characterized preferential ground-water seepage as part of an ongoing investigation of contaminant distribution and natural attenuation processes in wetlands at this site. Seep areas were discrete and spatially consistent during thermal infrared surveys in 2002, 2003, and 2004 throughout West Branch Canal Creek wetlands. In these seep areas, temperature measurements in shallow pore water and sediment more closely resembled those in ground water than those in nearby surface water. Generally, pore water in seep areas contaminated with chlorinated volatile organic compounds had lower methane and greater volatile organic compound concentrations than pore water in non-seep wetland sediments. The volatile organic compounds detected in shallow pore water in seeps were spatially similar to the dominant volatile organic compounds in the underlying Canal Creek aquifer, with both parent and anaerobic daughter compounds detected. Seep locations characterized as focused seeps contained the highest concentrations of chlorinated parent compounds

  8. Analysis of organo-chlorine pesticides residue in raw coffee with a modified "quick easy cheap effective rugged and safe" extraction/clean up procedure for reducing the impact of caffeine on the gas chromatography-mass spectrometry measurement.

    PubMed

    Bresin, Bruno; Piol, Maria; Fabbro, Denis; Mancini, Maria Antonietta; Casetta, Bruno; Del Bianco, Clorinda

    2015-01-01

    The control of pesticide residues on raw coffee is a task of great importance due to high consumption of this beverage in Italy and in many other countries. High caffeine content can hamper extraction and measurement of any pesticide residue. A tandem extraction protocol has been devised by exploiting the quick easy cheap effective rugged and safe (QuEChERS) scheme for extraction, coupled to a dispersive liquid-liquid micro-extraction (DLLME) in order to drastically reduce caffeine content in the final extract. Gas chromatography-mass spectrometry (GC-MS) has been used for quantification of organo-chlorine pesticides in single ion monitoring (SIM) mode. Method has been validated and performances meet the criteria prescribed by European Union regulations. PMID:25537171

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

    SciTech Connect

    Gordon, G.; Rosenblatt, A.

    1996-11-01

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

  10. Chlorine cyanide

    Integrated Risk Information System (IRIS)

    Chlorine cyanide ; CASRN 506 - 77 - 4 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic

  11. Chlorine dioxide

    Integrated Risk Information System (IRIS)

    Chlorine dioxide ; CASRN 10049 - 04 - 4 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogeni

  12. Estimation of polycyclic aromatic hydrocarbon concentrations in the water column based on tissue residues in mussels and salmon: An equilibrium partitioning approach

    SciTech Connect

    Neff, J.M.; Burns, W.A.

    1996-12-01

    Equilibrium partitioning was used to estimate concentrations of dissolved polycyclic aromatic hydrocarbons (PAHs) in the water column from PAH residues in tissues of mussels and juvenile pink salmon collected from coastal marine waters affected by the Exxon Valdez oil spill. Estimated concentrations were within factors of 2 to 5 for fish and 5 to 10 for mussels of average total dissolved and particulate PAHs measured in concurrent water samples. Temporal trends of estimated and measured water-column PAH concentrations were comparable. Water-column PAH concentrations estimated from residues in tissues of mussels (Mytilus trossulus) were higher than estimates based on residues in tissues of juvenile pink salmon (Oncorhynchus gorbuscha). Possible reasons for this difference include seasonal variations in mussel lipid content, differences in PAH uptake and depuration rates between fish and mussels, differences in how fish and mussels interact with particulate oil, and possible short exposure times for juvenile pink salmon. All of these factors may play a role. In any event, estimates of dissolved PAHs in the water column, based on PAH residues in either fish or mussel tissue, confirm that PAH concentrations generally did not exceed water quality standards for protection of marine life.

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

    PubMed

    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

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

    PubMed

    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.

  15. Chlorinated, brominated, and perfluorinated compounds, polycyclic aromatic hydrocarbons and trace elements in livers of sea otters from California, Washington, and Alaska (USA), and Kamchatka (Russia)

    USGS Publications Warehouse

    Kannan, K.; Moon, H.-B.; Yun, S.-H.; Agusa, T.; Thomas, N.J.; Tanabe, S.

    2008-01-01

    Concentrations of organochlorine pesticides (DDTs, HCHs, and chlordanes), polychlorinated biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs), polycyclic aromatic hydrocarbons (PAHs), perfluorinated compounds (PFCs), and 20 trace elements were determined in livers of 3- to 5-year old stranded sea otters collected from the coastal waters of California, Washington, and Alaska (USA) and from Kamchatka (Russia). Concentrations of organochlorine pesticides, PCBs, and PBDEs were high in sea otters collected from the California coast. Concentrations of DDTs were 10-fold higher in California sea otters than in otters from other locations; PCB concentrations were 5-fold higher, and PBDE concentrations were 2-fold higher, in California sea otters than in otters from other locations. Concentrations of PAHs were higher in sea otters from Prince William Sound than in sea otters from other locations. Concentrations of several trace elements were elevated in sea otters collected from California and Prince William Sound. Elevated concentrations of Mn and Zn in sea otters from California and Prince William Sound were indicative of oxidative stress-related injuries in these two populations. Concentrations of all of the target compounds, including trace elements, that were analyzed in sea otters from Kamchatka were lower than those found from the US coastal locations. ?? The Royal Society of Chemistry.

  16. Chlorinated hydrocarbon concentrations in plasma of the Lake Erie water snake (Nerodia sipedon insularum) and northern water snake (Nerodia sipedon sipedon) from the Great Lakes basin in 1998.

    PubMed

    Bishop, C A; Rouse, J D

    2000-11-01

    From the Great Lakes basin, concentrations of 59 congener-specific polychlorinated biphenyls (PCBs) and 14 organochlorine pesticides were measured in blood plasma of northern water snake (Nerodia sipedon sipedon) and Lake Erie water snake (Nerodia sipedon insularum), which is endangered in Canada. In 1998, four male adult Lake Erie water snakes were sampled from Pelee Island, western Lake Erie; four male northern water snakes were sampled at Little Lake, about 20 km north of Parry Sound in central Ontario; and four adult gravid female northern water snakes were sampled from Garden Island, eastern Lake Ontario. The blood plasma was pooled by site for a total of three samples analyzed. The Pelee Island sample from male Lake Erie water snakes contained less than half the lipid concentration (0.349%) than samples from the other sites, but it was the most contaminated with PCBs, even on a wet weight basis. Summed concentration of individual PCBs in the Pelee Island sample was 167 ng/g (wet weight), which was 14-fold higher than the next most contaminated sample, which was from Little Lake. The plasma sample from Little Lake contained 12 ng/g (WW) and was four times more contaminated with PCBs than the sample from female snakes from Garden Island, Lake Ontario. Organochlorine pesticide concentrations in plasma were relatively similar among sites. None of the pesticides was found above trace concentrations (0.1-0.9 ng/g) except pp'-DDE, which occurred at 2-5 ng/g among sites. PCB congener patterns in the Lake Erie water snakes were compared to PCB patterns in plasma of common snapping turtle (Chelydra serpentina serpentina) from Lake Ontario, herring gull eggs (Larus argentatus) from western Lake Erie, and mudpuppy eggs (Necturus maculosus) from the Detroit River. The PCB patterns in water snake and herring gull sample were most similar, followed by the pattern in snapping turtle plasma. The presence of more lower-chlorinated chlorobiphenyls in the mudpuppy eggs relative

  17. Chlorine Clues

    NASA Technical Reports Server (NTRS)

    2004-01-01

    This plot shows that levels of the element chlorine rise dramatically in the deeper rocks lining the walls of the crater dubbed 'Endurance.' The data shown here were taken by the Mars Exploration Rover Opportunity's alpha particle X-ray spectrometer at Endurance and 'Eagle Crater,' the site where Opportunity first landed at Meridiani Planum.

    Opportunity has been inching down the walls of Endurance Crater, investigating distinct layers of rock as it goes for clues to Mars' buried past. The various Endurance layers have been informally labeled 'A' through 'F.' Targets within these layers are listed on the graph along with previous targets from Eagle Crater. All the rocks listed here were observed after they had been drilled by the rover's rock abrasion tool.

    The observations indicate that the elements making up the shallow rock layers of Endurance Crater resemble those of Eagle, while the deeper layers of Endurance possess increasingly higher concentrations of the element chlorine.

    Opportunity will continue to roll deeper into Endurance to see if this puzzling trend continues. Scientists hope the new data will help them figure out how the presence of chlorine fits into the history of water at Endurance Crater.

  18. Pt/MgO as catalyst for hydrogenolysis reactions of C[sub 5] and C[sub 6] hydrocarbons: Evidence for metal-support interactions

    SciTech Connect

    Clarke, J.K.A.; Bradley, M.J. ); Garvie, L.A.J.; Craven, A.J.; Baird, T. )

    1993-09-01

    Pt/magnesia catalysts having high metal dispersion (av. dia. 21 [angstrom]) have been prepared employing nonaqueous impregnating solutions and an incipient wetness technique. Both chlorine-free and residual-chlorine-containing catalysts were studied, the latter being prepared from platinum (IV) chloride. Both types of catalyst are of negligible sulphur content (<2ppm). Comparison of hydrogen chemisorption and transmission electron microscopy results for both [open quotes]chlorine-free[close quotes] and chlorine-containing Pt/MgO catalysts showed that (i) chemisorption capacity was substantially as expected from TEM-derived particle size following a reduction temperature of 593 K (LTR), and (ii) chemisorption was depressed to 40% or less of expectation when a reduction temperature of 753 K (HTR) was used. Reactions of saturated hydrocarbons in a flow of hydrogen (p[sub hydrocarbon] = 8-16 Torr, balance to 760 Torr hydrogen) showed hydrogenolysis to be a prominent reaction. With LTR chlorine-free catalysts, hydrogenolysis of n-pentane was almost exclusively by central scission. The chlorine-containing HTR catalyst yielded largely terminal scission. HTR chlorine-free catalysts and LTR chlorine-containing catalysts gave an intermediate behavior. Thus, both higher reduction temperature and presence of chlorine act to move scission of the C-C chain from the center to the ends. Hydrogenolysis of neohexane showed increased direct demethanation to give n-butane with the presence of chlorine in the catalyst. Ring scission of methylcyclopentane depressed hydrogen chemisorption and the carbanionic reactivity in these cracking reactions are interpreted in terms of a moderately strong metal-support interaction with a shift of negative charge from the magnesia O[sup 2[minus

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

    SciTech Connect

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

    1986-11-01

    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 pipe were added for circulation. The levels of residual disinfectants tested were 0.2 mg/L and 1.0 mg/L as available chlorine. In the absence of a disinfectant residual, microorganisms in the sewage contaminant were consistently recovered at high levels. The presence of any disinfectant residual reduced the microorganism level and frequency of occurrence at the consumer's tap. Free chlorine was the most effective residual disinfectant and may serve as a marker or flag in the distribution network. Free chlorine and chlorine dioxide were the least stable in the pipe network. The loss of disinfectant in the pipe network followed first-order kinetics. The half-life determined in static tests for free chlorine, chlorine dioxide, and combined chlorine was 140, 93, and 1680 min.

  20. TREATMENT OF HYDROCARBON, ORGANIC RESIDUE AND PRODUCTION CHEMICAL DAMAGE MECHANISMS THROUGH THE APPLICATION OF CARBON DIOXIDE IN NATURAL GAS STORAGE WELLS

    SciTech Connect

    Lawrence J. Pekot; Ron Himes

    2004-05-31

    Core specimens and several material samples were collected from two natural gas storage reservoirs. Laboratory studies were performed to characterize the samples that were believed to be representative of a reservoir damage mechanism previously identified as arising from the presence of hydrocarbons, organic residues or production chemicals. A series of laboratory experiments were performed to identify the sample materials, use these materials to damage the flow capacity of the core specimens and then attempt to remove or reduce the induced damage using either carbon dioxide or a mixture of carbon dioxide and other chemicals. Results of the experiments showed that pure carbon dioxide was effective in restoring flow capacity to the core specimens in several different settings. However, in settings involving asphaltines as the damage mechanism, both pure carbon dioxide and mixtures of carbon dioxide and other chemicals provided little effectiveness in damage removal.

  1. Polycyclic Aromatic Hydrocarbons Residues in Gentile Di Maiale, a Smoked Meat Product Typical of Some Mountain Areas in Latina Province (Central Italy)

    PubMed Central

    Carrabs, Giuseppe; Mercogliano, Raffaelina; Carosielli, Leonardo; Vollano, Lucia; Anastasio, Aniello

    2014-01-01

    Gentile di maiale is a typical meat product prepared in some traditional plants of Latina Province (Central Italy). It is obtained from dehydration, salting, smoking and ripening of swine rectum. Aim of this study was to evaluate the influence of the traditional smoking process on polycyclic aromatic hydrocarbons (PAHs) content by means of high-performance liquid chromatographic/fluorescence detection. Polycyclic aromatic hydrocarbons detected in 8 samples of raw material (swine rectum) and samples of smoked gentile were: benzo[a]anthracene, chrisene, benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[a] pyrene, benzo[a,h]anthracene. Their residues were detected in all samples of finished product. European Regulation 835/2011 established two levels of PAHs content in meat products. According to first levels, in force until September 2014, only 2 out of 8 samples exceeded legal limit. According to the subsequent, more restrictive, limits all samples would be non-compliant. An improvement and a standardisation of traditional smoking procedures are recommended. PMID:27800340

  2. TREATMENT OF HYDROCARBON, ORGANIC RESIDUE AND PRODUCTION CHEMICAL DAMAGE MECHANISMS THROUGH THE APPLICATION OF CARBON DIOXIDE IN NATURAL GAS STORAGE WELLS

    SciTech Connect

    Lawrence J. Pekot

    2004-06-30

    Two gas storage fields were studied for this project. Overisel field, operated by Consumer's Energy, is located near the town of Holland, Michigan. Huntsman Storage Unit, operated by Kinder Morgan, is located in Cheyenne County, Nebraska near the town of Sidney. Wells in both fields experienced declining performance over several years of their annual injection/production cycle. In both fields, the presence of hydrocarbons, organic materials or production chemicals was suspected as the cause of progressive formation damage leading to the performance decline. Core specimens and several material samples were collected from these two natural gas storage reservoirs. Laboratory studies were performed to characterize the samples that were believed to be representative of a reservoir damage mechanism previously identified as arising from the presence of hydrocarbons, organic residues or production chemicals. A series of laboratory experiments were performed to identify the sample materials, use these materials to damage the flow capacity of the core specimens and then attempt to remove or reduce the induced damage using either carbon dioxide or a mixture of carbon dioxide and other chemicals. Results of the experiments showed that pure carbon dioxide was effective in restoring flow capacity to the core specimens in several different settings. However, in settings involving asphaltines as the damage mechanism, both pure carbon dioxide and mixtures of carbon dioxide and other chemicals provided little effectiveness in damage removal.

  3. Chlorine Analysis - Water. Training Module 5.260.2.77.

    ERIC Educational Resources Information Center

    Kirkwood Community Coll., Cedar Rapids, IA.

    This document is an instructional module package prepared in objective form for use by an instructor familiar with the procedures for chlorine residual analysis. It includes objectives, an instructor guide, and student handouts. The module addresses the determination of combined and free residual chlorine in water supply samples using three…

  4. Toxicity of chlorinated insecticides to quail and pheasants

    USGS Publications Warehouse

    DeWitt, J.B.

    1956-01-01

    'Residues from insecticidal applications of chlorinated hydrocarbons may remain toxic for extended periods. In experiments designed to furnish information on the effects upon quail and pheasants of prolonged feeding upon diets containing small percentages of these compounds, it was shown that aldrin, dieldrin and endrin are cumulative, and that quail are unable to survive after ingesting 5-10 mg./kg, of aldrin, 30-50 mg./kg, of dieldrin, or 6-15 mg./kg, of endrin. Maximum levels (p.p.m.) in the diets permitting survival for extended periods were: DDT, 200; strobane, above 500; aldrin, 0.5; dieldrin, 1.0; endrin, 1.0. Inclusion of these compounds in the diets of breeding quail and pheasants affected hatchability of eggs and viability of chicks, even though the adult birds appeared unaffected.' Detailed figures are given for all points mentioned.

  5. [Residues and risk assessment of polycyclic aromatic hydrocarbons in the surface sediments and marine organisms from Dapeng Bay, Shenzhen].

    PubMed

    Sun, Run-Xia; Ke, Chang-Liang; Gu, Yang-Guang; Lu, Teng-Teng; Du, Fei-Yan; Ma, Sheng-Wei; Lin, Qin

    2013-10-01

    In order to assess contamination by polycyclic aromatic hydrocarbons (PAHs), surface sediments and marine organism samples of fish, shrimp and shellfish were collected from the Dapeng Bay, Shenzhen in October 2011. Concentrations fof sixteen priority PAHs were determined by gas chromatography and mass spectrometry (GC-MS). The total concentrations of PAHs (Sigma PAHs ) ranged from 216. 56 ng.g-1 to 1 314. 92 ng.g-1 dry weight in sediment samples and from 70. 88 ng.g-1 to 251.90 ng.g-1 wet weight in biological samples, respectively. The mean concentration was the highest in fish (171.52 ng.g-1 ), followed by mussel (134.75 ng.g-1) and shrimp (123.35 ng.g-1) in the studied marine organisms. Compared with those in other water bodies around the world, PAHs pollution in the studied area was at medium level. The dominant fraction in the surface sediments was the 4-ring PAHs. Identification of PAH sources suggested that PAHs in Dapeng Bay were likely originated from both pyrolytic and petrogenic sources. The most abundant PAHs were 3-ring PAHs in the tissues of organisms, which may be governed by their feeding behaviors, habitats, and bioavailability of PAHs. Ecological risk assessment indicated that PAHs in surface sediments might have adverse impacts on local ecosystem. Health risk analysis revealed that the potency equivalent concentrations of BaP to the total PAHs in marine organisms from Dapeng Bay were relatively high and may cause some concerns on human health by consumption.

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

    SciTech Connect

    Garrett, W.E. Jr.

    1995-06-01

    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.

  7. Distribution of polycyclic aromatic hydrocarbon (PAH) residues in several tissues of edible fishes from the largest freshwater lake in China, Poyang Lake, and associated human health risk assessment.

    PubMed

    Zhao, Zhonghua; Zhang, Lu; Cai, Yongjiu; Chen, Yuwei

    2014-06-01

    The residual levels, tissue distribution and human health risk assessment of polycyclic aromatic hydrocarbons (PAHs) in edible fishes, bighead carp (Aristichthys nobilis) and silver carp (Hypophthalmichthys molitrix), from the largest freshwater lake in China, Poyang Lake, were studied. PAH concentrations ranged from 105 to 513ng g(-1)ww and from 53.9 to 401ng g(-1)ww in different tissues of bighead carp and silver carp, respectively. Low molecular weight (LMW) PAHs were the predominant compounds, suggesting the gill-water transfer might be the major exposure route for PAHs in the studied fish species. Tissue distribution indicated that the hepatobiliary system accumulated higher concentrations of PAHs than the extrahepatic tissues with bile being the most predominant tissue for both species. Composition analysis demonstrated that PAHs were from the combined petrogenic and pyrogenic origin, and the gasoline combustion might be the main source. A preliminary evaluation of human health risk using benzo[a]pyrene (BaP) potency equivalent concentration (PEC) as well as the incremental lifetime cancer risk (ILCR) indicated that PAHs in fish would induce potential carcinogenic effects. PMID:24732028

  8. Organochlorine residues in two Norwegian puffin (Fratercula arctica) colonies.

    PubMed

    Ingebrigtsen, K; Skaare, J U; Teigen, S W

    1984-01-01

    Residue levels of the chlorinated hydrocarbons hexachlorobenzene (HCB), polychlorinated biphenyls (PCBs), alpha-, beta-, and gamma-hexachlorocyclohexane (HCH), oxychlordane, trans-nonachlor, aldrin, and dieldrin in adult puffins (Fratercula arctica) from two colonies in Norway (Røst 67 degrees 30'N and Hornøy 70 degrees 20'N) showing differences in breeding performance were compared in 1982. Furthermore, residue levels in puffin chicks from Røst in 1982, when breeding failed totally, were compared with the corresponding levels in 1983, when breeding was successful. Residue levels of chlorinated hydrocarbons were also measured in eggs from Røst 1982. An autoradiographic study of the distribution of [14C]HCB in adult puffins and chicks from Røst 1982 was included. In general, organochlorine contamination was low, and the results are interpreted to eliminate the organochlorines as a serious factor for impaired reproduction in the Røst colony. Significant differences between the two colonies are discussed in relation to geographical and nutritional aspects. The finding of significantly higher levels of organochlorines in organ tissue from puffin chicks from Røst in 1982 compared to the corresponding levels in 1983 may reflect the dramatic difference in nutritional status between the two years. PMID:6084067

  9. Hydrocarbon pneumonia

    MedlinePlus

    Pneumonia - hydrocarbon ... Coughing Fever Shortness of breath Smell of a hydrocarbon product on the breath Stupor (decreased level of ... Most children who drink or inhale hydrocarbon products and develop ... hydrocarbons may lead to rapid respiratory failure and death.

  10. Optimizing booster chlorination in water distribution networks: a water quality index approach.

    PubMed

    Islam, Nilufar; Sadiq, Rehan; Rodriguez, Manuel J

    2013-10-01

    The optimization of chlorine dosage and the number of booster locations is an important aspect of water quality management in distribution networks. Booster chlorination helps to maintain uniformity and adequacy of free residual chlorine concentration, essential for safeguarding against microbiological contamination. Higher chlorine dosages increase free residual chlorine concentration but generate harmful by-products, in addition to taste and odor complaints. It is possible to address these microbial, chemical, and aesthetic water quality issues through free residual chlorine concentration. Estimating a water quality index (WQI) based on regulatory chlorine thresholds for microbial, chemical, and aesthetics criteria can help engineers make intelligent decisions. An innovative scheme for maintaining adequate residual chlorine with optimal chlorine dosages and numbers of booster locations was established based on a proposed WQI. The City of Kelowna (BC, Canada) water distribution network served to demonstrate the application of the proposed scheme. Temporal free residual chlorine concentration predicted with EPANET software was used to estimate the WQI, later coupled with an optimization scheme. Preliminary temporal and spatial analyses identified critical zones (relatively poor water quality) in the distribution network. The model may also prove useful for small or rural communities where free residual chlorine is considered as the only water quality criterion.

  11. The Chlorination Quandary

    ERIC Educational Resources Information Center

    Josephson, Julian

    1978-01-01

    Current use of chlorination technology to disinfect water supplies can cause the production of undesirable products, among them chloroform and chlorobenzene. Alternatives to this methodology include the use of ozone, chlorine dioxide, and bromine chloride in place of chlorine. Presently, the methods are feasible in developed countries only. (MA)

  12. Biodegration of chlorinated ethenes

    USGS Publications Warehouse

    Bradley, Paul M.; Chapelle, Francis H.

    2010-01-01

    Biodegradation of chlorinated ethenes by naturally occurring or artificially enhanced processes is an important component of current site remediation strategies. At this writing, several microbial mechanisms for chlorinated ethene transformation and degradation have been identified. The purpose of this chapter is to briefly summarize the current understanding of those processes that lead to the biodegradation of chlorinated ethenes.

  13. Water chlorination Vol. 5

    SciTech Connect

    Jolley, R.L.; Bull, R.J.; Davis, W.P.; Katz, S.; Roberts, M.H.

    1985-01-01

    This book describes the significant original contributions in the field of water chlorination of the last three years. It includes chlorination research, developments and alternatives. Issues covered include: water chlorination; risk; epidemiology; carcinogenic and mutagenic effects; toxicology of disinfectants; aquatic models and tumor induction; environmental effects; disinfection; reaction dynamics; chemical methods; drinking water treatment and wastewater treatment.

  14. The Galeta Oil Spill. III. Chronic Reoiling, Long-term Toxicity of Hydrocarbon Residues and Effects on Epibiota in the Mangrove Fringe

    NASA Astrophysics Data System (ADS)

    Levings, Sally C.; Garrity, Stephen D.; Burns, Kathryn A.

    1994-04-01

    In April 1986, 75 000-100 000 barrels of medium-weight crude oil (˜ 10 000-13 500 metric tons) spilled into Bahı´a las Minas, a large mangrove-lined bay on the Caribbean coast of Panamá. Between 1986 and 1991, biological and chemical effects of this spill were studied. The epibiota of fringing mangroves ( Rhizophora mangle L.) were examined in three habitats: (1) the shoreward margins of reef flats that fronted the open sea, (2) the edges of channels and lagoons, and (3) the banks of streams and man-made cuts that drained interior mangroves or uplands into lagoons. Chemical analyses of bivalves collected from submerged prop roots (oysters and false mussels) and records of slicks and tarry deposits on artificial roots documented chronic reoiling. Each habitat was repeatedly oiled between 1986 and 1991, with petroleum residues identified as the oil spilled in 1986. There was a decline in the release of tarry oils recorded as slicks and on roots over time, but not in tissue burdens of hydrocarbons in bivalves. This suggested that the processes that released these different types of oil residues were at least partially independent and that toxic hydrocarbons were likely to be released from sediments over the long term. The submerged prop roots of fringing mangroves in each habitat had a characteristic epibiota. On the open coast, roots were covered with a diverse assemblage of sessile invertebrates and algae. In channels, the most abundant species on roots was the edible oyster Crassostrea virginica ( rhizophorae morph). In streams, the false mussel Mytilopsis sallei covered the most space on roots. Cover of sessile invertebrates was significantly reduced at oiled compared with unoiled sites on the open coast for 4 years after oiling, while oysters and false mussels were reduced in cover at oiled sites in channels and streams through at least 1991, when observations ended. False mussels transplanted from an unoiled stream to oiled and unoiled streams were

  15. Bioavailability of polycyclic aromatic hydrocarbons from buried shoreline oil residues thirteen years after the Exxon Valdez oil spill: a multispecies assessment.

    PubMed

    Neff, Jerry M; Bence, A Edward; Parker, Keith R; Page, David S; Brown, John S; Boehm, Paul D

    2006-04-01

    Seven taxa of intertidal plants and animals were sampled at 17 shoreline sites in Prince William Sound ([PWS]; AK, USA), that were heavily oiled in 1989 by the Exxon Valdez oil spill (EVOS) to determine if polycyclic aromatic hydrocarbons (PAH) from buried oil in intertidal sediments are sufficiently bioavailable to intertidal prey organisms that they might pose a health risk to populations of birds and wildlife that forage on the shore. Buried residues of EVOS oil are present in upper and middle intertidal sediments at 16 sites. Lower intertidal (0 m) sediments contain little oil. Much of the PAH in lower intertidal sediments are from combustion sources. Mean tissue total PAH (TPAH) concentrations in intertidal clams, mussels, and worms from oiled sites range from 24 to 36 ng/g (parts per billion) dry weight; sea lettuce, whelks, hermit crabs, and intertidal fish contain lower concentrations. Concentrations of TPAH are similar or slightly lower in biota from unoiled reference sites. The low EVOS PAH concentrations detected in intertidal biota at oiled shoreline sites indicate that the PAH from EVOS oil buried in intertidal sediments at these sites have a low bioavailability to intertidal plants and animals. Individual sea otters or shorebirds that consumed a diet of intertidal clams and mussels exclusively from the 17 oiled shores in 2002 were at low risk of significant health problems. The low concentrations of EVOS PAH found in some intertidal organisms at some oiled shoreline sites in PWS do not represent a health risk to populations of marine birds and mammals that forage in the intertidal zone. PMID:16629134

  16. Bioavailability of polycyclic aromatic hydrocarbons from buried shoreline oil residues thirteen years after the Exxon Valdez oil spill: a multispecies assessment.

    PubMed

    Neff, Jerry M; Bence, A Edward; Parker, Keith R; Page, David S; Brown, John S; Boehm, Paul D

    2006-04-01

    Seven taxa of intertidal plants and animals were sampled at 17 shoreline sites in Prince William Sound ([PWS]; AK, USA), that were heavily oiled in 1989 by the Exxon Valdez oil spill (EVOS) to determine if polycyclic aromatic hydrocarbons (PAH) from buried oil in intertidal sediments are sufficiently bioavailable to intertidal prey organisms that they might pose a health risk to populations of birds and wildlife that forage on the shore. Buried residues of EVOS oil are present in upper and middle intertidal sediments at 16 sites. Lower intertidal (0 m) sediments contain little oil. Much of the PAH in lower intertidal sediments are from combustion sources. Mean tissue total PAH (TPAH) concentrations in intertidal clams, mussels, and worms from oiled sites range from 24 to 36 ng/g (parts per billion) dry weight; sea lettuce, whelks, hermit crabs, and intertidal fish contain lower concentrations. Concentrations of TPAH are similar or slightly lower in biota from unoiled reference sites. The low EVOS PAH concentrations detected in intertidal biota at oiled shoreline sites indicate that the PAH from EVOS oil buried in intertidal sediments at these sites have a low bioavailability to intertidal plants and animals. Individual sea otters or shorebirds that consumed a diet of intertidal clams and mussels exclusively from the 17 oiled shores in 2002 were at low risk of significant health problems. The low concentrations of EVOS PAH found in some intertidal organisms at some oiled shoreline sites in PWS do not represent a health risk to populations of marine birds and mammals that forage in the intertidal zone.

  17. Bioremediation and phytoremediation: Chlorinated and recalcitrant compounds

    SciTech Connect

    1998-12-31

    Bioremediation and phytoremediation have progressed, especially with regard to the treatment of hydrocarbon-contaminated sites. Sites contaminated with chlorinated and recalcitrant compounds have proven more resistant to these approaches, but exciting progress is being made both in the laboratory and in the field. This book brings together the latest breakthrough thinking and results in bioremediation, with chapters on cometabolic processes, aerobic and anaerobic mechanisms, biological reductive dechlorination processes, bioaugmentation, biomonitoring, and phytoremediation of recalcitrant organic compounds.

  18. PCDD/F and related compounds in solid residues from municipal solid waste incineration--a literature review.

    PubMed

    Vehlow, Jürgen; Bergfeldt, Britta; Hunsinger, Hans

    2006-10-01

    Emissions of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/F) from waste incineration into the air have been a major focus of interest during the last two decades. An integrated approach to clean waste disposal has to take the occurrence of PCDD/F in all residues into account. This paper compiles published data on concentration ranges of PCDD/F and the related compounds polychlorinated biphenyls (PCB), chlorinated benzenes and phenols, as well as polyaromatic hydrocarbons (PAH) in solid residues from waste incineration in grate furnaces and their development since 1985. A short description of inertization processes for PCDD/F loaded materials is added.

  19. Precision Cleaning Verification of Nonvolatile Residues by Using Water, Ultrasonics, and Turbidity Analyses

    NASA Technical Reports Server (NTRS)

    Skinner, S. Ballou

    1991-01-01

    Chlorofluorocarbons (CFC's) in the atmosphere are believed to present a major environmental problem because they are able to interact with and deplete the ozone layer. NASA has been mandated to replace chlorinated solvents in precision cleaning, cleanliness verification, and degreasing of aerospace fluid systems hardware and ground support equipment. KSC has a CFC phase-out plan which provides for the elimination of over 90 percent of the CFC and halon use by 1995. The Materials Science Laboratory and KSC is evaluating four analytical methods for the determination of nonvolatile residues removal by water: (1) infrared analyses using an attenuated total reflectance; (2) surface tension analyses, (3) total organic content analyses, and (4) turbidity analyses. This research project examined the ultrasonic-turbidity responses for 22 hydrocarbons in an effect to determine: (1) if ultrasonics in heated water (70 C) will clean hydrocarbons (oils, greases, gels, and fluids) from aerospace hardware; (2) if the cleaning process by ultrasonics will simultaneously emulsify the removed hydrocarbons in the water; and (3) if a turbidimeter can be used successfully as an analytical instrument for quantifying the removal of hydrocarbons. Sixteen of the 22 hydrocarbons tested showed that ultrasonics would remove it at least 90 percent of the contaminated hydrocarbon from the hardware in 10 minutes or less giving a good ultrasonic-turbidity response. Six hydrocarbons had a lower percentage removal, a slower removal rate, and a marginal ultrasonic-turbidity response.

  20. All About Chlorinated Carbon Nanotubes

    NASA Astrophysics Data System (ADS)

    Erbahar, Dogan; Berber, Savas

    2011-03-01

    The halogens are viable alternatives to harsher chemicals in the post-process of purification of carbon nanotube production. However the chlorine is known to bind less agresively to carbon nanotubes than fluorine and hydrogen. Therefore, in principle the residual Cl left after the halogen gas treatment of the nanotubes can be removed without damaging the nanotube walls easier. We report ab initio density functional calculation results about pure and defective carbon nanotubes of various diameters interacting with single and multiple chlorine atoms. We first focus on pure nanotubes and investigate the adsorption of additional Cl atoms near the first adsorbtion site, investigate the clustering tendency and most favourable configurations. We report the energetics results as well as the alteration of electronic properties. We then focus on monovacancy and divacancy defects on carbon nanotubes. It is a known fact that the defective site to be more active in this case. We apply the same procedure as in the pure nanotubes but also investigate the effect of chlorination on reconstruction process and also electronic transport properties. Supported by TUBITAK Grant No 108T740.

  1. Bioremediation of chlorinated benzene compounds

    SciTech Connect

    Peck, P.C.; Rhodes, S.H.; Guerin, T.F.

    1995-12-31

    In early 1994, investigations at a pharmaceutical manufacturing site revealed extensive areas of soil contaminated with chlorinated benzenes. The soil was a heavy clay and contained chlorobenzene (CB), 1,2-dichlorobenzene (referred to in this paper as DCB), and small amounts of 1,3- and 1,4-dichlorobenzene and other solvents. The soil was bioremediated in a pilot-scale treatment using an ex situ process with various inorganic and organic amendments. Approximately 90% of the DCB mass present in the soil was removed over a period of 2 to 3 weeks. Up to 100-fold increases in both total heterotrophs and specific degraders were observed. Residual concentrations of chlorinated benzenes were generally below detection limits. Adding organic matter did not appear to significantly enhance the treatment efficiency. Mass balance calculations applied to the treatment indicated that less than 5% of the chlorinated benzenes were removed by volatilization. Evidence was obtained that approximately 90% of the DCB was removed by biodegradation in these pilot-scale trials. Laboratory shake flask trials were conducted which confirmed that the soils in the pilot-scale treatment contained microorganisms capable of mineralizing CB and DCB.

  2. Atomic scale insights on chlorinated gamma-alumina surfaces.

    PubMed

    Digne, Mathieu; Raybaud, Pascal; Sautet, Philippe; Guillaume, Denis; Toulhoat, Hervé

    2008-08-20

    The thermochemistry of chlorinated gamma-alumina surfaces is explored by means of density functional calculations as a function of relevant reaction conditions used in experiments and in high-octane fuel production in the refining industry such as hydrocarbon isomerization and reforming. The role of chlorine as a dope of the Brønsted acidity of gamma-alumina surfaces is investigated at an atomic scale. Combining infrared spectroscopy and density functional theory calculations, the most favorable location of chlorine atoms on the (110), (100) and (111) surfaces of gamma-alumina is found to result either from direct adsorption or from the exchange of basic hydroxyl groups. Moreover, the modification of the hydrogen bond network upon chlorine adsorption is put forward as a key parameter for changing the Brønsted acidity. In a second step, we use a thermodynamic approach based on DFT total energy calculations corrected by the chemical potentials of HCl and H2O to determine the adsorption isotherms of chlorine and the relative surface concentration of hydroxyl groups and chlorine species on the gamma-alumina surfaces. The determination of chlorine content as a function of temperature and partial pressures of H2O and HCl offers new quantitative data required for optimizing the state of the support surface in industrial conditions. The mechanisms of chlorination are also discussed as a function of reaction conditions. PMID:18646849

  3. Recovering hydrocarbons from hydrocarbon-containing vapors

    DOEpatents

    Mirza, Zia I.; Knell, Everett W.; Winter, Bruce L.

    1980-09-30

    Values are recovered from a hydrocarbon-containing vapor by contacting the vapor with quench liquid consisting essentially of hydrocarbons to form a condensate and a vapor residue, the condensate and quench fluid forming a combined liquid stream. The combined liquid stream is mixed with a viscosity-lowering liquid to form a mixed liquid having a viscosity lower than the viscosity of the combined liquid stream to permit easy handling of the combined liquid stream. The quench liquid is a cooled portion of the mixed liquid. Viscosity-lowering liquid is separated from a portion of the mixed liquid and cycled to form additional mixed liquid.

  4. Water Treatment Technology - Chlorination.

    ERIC Educational Resources Information Center

    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…

  5. Photochemical chlorine activation from artificial saline snowpacks

    NASA Astrophysics Data System (ADS)

    Wren, Sumi; Donaldson, James; Abbatt, Jon

    2013-04-01

    Halogen activation on snow and ice substrates has a profound influence on the oxidative capacity of the polar boundary layer. The release of reactive chlorine species is of particular interest since chlorine atoms can participate in both ozone depletion and hydrocarbon oxidation. However, the mechanisms by which halides in sea ice substrates are converted into reactive halogen species are not well understood. In this study we investigated the activation of halogens from artificial saline snow in the presence of light and ozone. Gas phase Cl2, BrCl and Br2 were detected using a chemical ionization mass spectrometer. We observe the dark release of Br2 in the presence of ozone; BrCl and Cl2 are only observed in the presence of both ozone and light. Interestingly, photo-induced release of halogens is still seen when a 320 nm or a 380 nm long-pass filter is placed in the light path. The observed halogen release is consistent with the chemistry occurring in a concentrated brine located at the surface of the snow grains. Results suggest that smaller snow grains, which present a larger total snow surface area, enhance chlorine production to a greater extent than BrCl or Br2 production. Chlorine production is shown to be strongly pH dependent, with higher chlorine yields under acidic conditions. Overall the results indicate that a mechanism involving UV-A light and ozone leads to accelerated halogen activation, which may be particularly important for releasing chlorine from bromide-depleted snow.

  6. Chlorine dioxide treatment for zebra mussel control

    SciTech Connect

    Rybarik, D.; Byron, J.; Germer, M.

    1995-06-01

    Chlorine is recognized and commonly used biocide for power plant cooling water and service water treatment programs, including the control of zebra mussels. Chlorine dioxide has recently become a popular method of zebra mussel control because of its economy, safety, environmental acceptability, and effectiveness when compared to other mussel control methods. This control technique was recently demonstrated at Dairyland Power Cooperative`s Alma Generating Station on the east bank of the upper Mississippi River in Alma, Wisconsin. The project was assisted with EPRI Tailored Collaboration Program funds. The Dairyland Power Alam Generating Station consists of five generating units that utilize raw, untreated Mississippi River water for condenser, circulating, and service water supplies. The first units were built in 1947, with the final and largest unit being completed in 1960. Total station generating capacity is 200 MW. Because of recent increases in the zebra mussel density at the station intake, Dairyland Power selected the team of Nalco and Rio Linda to perform a chlorine dioxide treatment of the station`s new water systems to eradicate and control the mussels before their presence created operational difficulties. This paper will present the results of the treatment including treatment theory, design and construction of the treatment system, the method of chlorine dioxide generation, treatment concentration, analytical methods o monitoring chlorine dioxide generation, residuals and trihalomethane (THM) concentrations, protocol for monitoring treatment mortality, and the effects of chlorine dioxide and detoxification on other water chemistry parameters and equipment materials. The goal of this paper is to inform and assist users with establishing consistent and uniform practices for safely utilizing and monitoring chlorine dioxide in the eradication and control of zebra mussels.

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

    PubMed

    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.

  8. TECHNICAL PROTOCOL FOR EVALUATING NATURAL ATTENUATION OF CHLORINATED SOLVENTS IN GROUND WATER

    EPA Science Inventory

    This Protocol is designed to evaluate the fate in ground water of chlorinated aliphatic hydrocarbons and/or fuel hydrocarbons. Documentation of natural attenuation requires detailed site characterization. The data collected under this protocol can be used to compare the relati...

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

    PubMed

    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

  10. Evaluation of the Tenax trap in the Sample Analysis at Mars instrument suite on the Curiosity rover as a potential hydrocarbon source for chlorinated organics detected in Gale Crater

    NASA Astrophysics Data System (ADS)

    Miller, Kristen E.; Kotrc, Benjamin; Summons, Roger E.; Belmahdi, Imene; Buch, Arnaud; Eigenbrode, Jennifer L.; Freissinet, Caroline; Glavin, Daniel P.; Szopa, Cyril

    2015-08-01

    The Sample Analysis at Mars (SAM) instrument suite aboard Curiosity has detected chlorinated organic compounds in Martian sediment samples. The chlorine in these molecules is thought to derive from oxychlorine salts in Martian sediments, but the carbon source remains under investigation. To constrain possible carbon sources, we investigated how the composition and concentration of oxychlorine phases in solid samples affect organic molecules released from the Tenax traps on board SAM. We created Mars analogue soils by spiking olivine sand with calcium perchlorate, magnesium perchlorate, or ferric iron chloride and analyzed the volatiles generated during pyrolysis-gas chromatography-mass spectrometry using commercial instruments operated under SAM-like conditions, with and without a Tenax trap. Benzoic acid, phthalic anhydride, high molecular weight aromatics, and chlorobenzenes are produced from the trap in response to volatiles released during Cl salt pyrolysis. Changes in composition or concentration of oxychlorine phases between samples could thus potentially produce an increase in chlorobenzene, as observed between samples from Rocknest and Cumberland. However, in our experiments benzoic acid, phthalic anhydride, and chlorobenzenes increase in proportion with the amount of HCl sent to the trap, while in Cumberland samples the chlorobenzene increase showed no corresponding increase in HCl. Based on our experiments, the Tenax trap is a possible source of the traces of chlorobenzene observed at Rocknest, John Klein, and Confidence Hills. The order-of-magnitude higher chlorobenzene abundances observed at Cumberland cannot be attributed to the Tenax trap. Furthermore, we found no evidence of significant trap degradation after hundreds of experiments with Cl salt-containing analogue soils.

  11. Assessing fuel spill risks in polar waters: Temporal dynamics and behaviour of hydrocarbons from Antarctic diesel, marine gas oil and residual fuel oil.

    PubMed

    Brown, Kathryn E; King, Catherine K; Kotzakoulakis, Konstantinos; George, Simon C; Harrison, Peter L

    2016-09-15

    As part of risk assessment of fuel oil spills in Antarctic and subantarctic waters, this study describes partitioning of hydrocarbons from three fuels (Special Antarctic Blend diesel, SAB; marine gas oil, MGO; and intermediate grade fuel oil, IFO 180) into seawater at 0 and 5°C and subsequent depletion over 7days. Initial total hydrocarbon content (THC) of water accommodated fraction (WAF) in seawater was highest for SAB. Rates of THC loss and proportions in equivalent carbon number fractions differed between fuels and over time. THC was most persistent in IFO 180 WAFs and most rapidly depleted in MGO WAF, with depletion for SAB WAF strongly affected by temperature. Concentration and composition remained proportionate in dilution series over time. This study significantly enhances our understanding of fuel behaviour in Antarctic and subantarctic waters, enabling improved predictions for estimates of sensitivities of marine organisms to toxic contaminants from fuels in the region. PMID:27389459

  12. Assessing fuel spill risks in polar waters: Temporal dynamics and behaviour of hydrocarbons from Antarctic diesel, marine gas oil and residual fuel oil.

    PubMed

    Brown, Kathryn E; King, Catherine K; Kotzakoulakis, Konstantinos; George, Simon C; Harrison, Peter L

    2016-09-15

    As part of risk assessment of fuel oil spills in Antarctic and subantarctic waters, this study describes partitioning of hydrocarbons from three fuels (Special Antarctic Blend diesel, SAB; marine gas oil, MGO; and intermediate grade fuel oil, IFO 180) into seawater at 0 and 5°C and subsequent depletion over 7days. Initial total hydrocarbon content (THC) of water accommodated fraction (WAF) in seawater was highest for SAB. Rates of THC loss and proportions in equivalent carbon number fractions differed between fuels and over time. THC was most persistent in IFO 180 WAFs and most rapidly depleted in MGO WAF, with depletion for SAB WAF strongly affected by temperature. Concentration and composition remained proportionate in dilution series over time. This study significantly enhances our understanding of fuel behaviour in Antarctic and subantarctic waters, enabling improved predictions for estimates of sensitivities of marine organisms to toxic contaminants from fuels in the region.

  13. Polycyclic aromatic hydrocarbon body residues and lysosomal membrane destabilization in mussels exposed to the Dubai Star bunker fuel oil (intermediate fuel oil 380) spill in San Francisco Bay.

    PubMed

    Hwang, Hyun-Min; Stanton, Beckye; McBride, Toby; Anderson, Michael J

    2014-05-01

    Following the spill of bunker fuel oil (intermediate fuel oil 380, approximately 1500-3000 L) into San Francisco Bay in October 2009, polycyclic aromatic hydrocarbon (PAH) concentrations in mussels from moderately oiled areas increased up to 87 554 ng/g (dry wt) and, 3 mo later, decreased to concentrations found in mussels collected prior to oiling, with a biological half-life of approximately 16 d. Lysosomal membrane destabilization increased in mussels with higher PAH body burdens.

  14. CHLORINATED SOLVENT PLUME CONTROL

    EPA Science Inventory

    This lecture will cover recent success in controlling and assessing the treatment of shallow ground water plumes of chlorinated solvents, other halogenated organic compounds, and methyl tert-butyl ether (MTBE).

  15. Breathing with chlorinated solvents

    SciTech Connect

    McCarty, P.L.

    1997-06-06

    Chlorinated solvents are effective cleaners and in the past dirted solvents were dumped into landfills, stored in tanks that often leaked, or spilled. As a result the most common contaminants of organic groundwater at hazardous waste sites are the two major chlorinated solvents - tetrachloroethylene (PCE) and trichloroethylene (TCE). Both are suspected carcinogens and both are highly resistant to biodegradation. Now however, there is a report of a bacterium that can remove all of the chlorine atoms from both by halorespiration to form ethene, an innocuous end product. This article goes on to discuss the background of biodegradation of chlorinated compounds, why it is so difficult, and what the future is in this area. 9 refs., 1 fig.

  16. Sarcoendoplasmic reticulum Ca(2+) ATPase. A critical target in chlorine inhalation-induced cardiotoxicity.

    PubMed

    Ahmad, Shama; Ahmad, Aftab; Hendry-Hofer, Tara B; Loader, Joan E; Claycomb, William C; Mozziconacci, Olivier; Schöneich, Christian; Reisdorph, Nichole; Powell, Roger L; Chandler, Joshua D; Day, Brian J; Veress, Livia A; White, Carl W

    2015-04-01

    Autopsy specimens from human victims or experimental animals that die due to acute chlorine gas exposure present features of cardiovascular pathology. We demonstrate acute chlorine inhalation-induced reduction in heart rate and oxygen saturation in rats. Chlorine inhalation elevated chlorine reactants, such as chlorotyrosine and chloramine, in blood plasma. Using heart tissue and primary cardiomyocytes, we demonstrated that acute high-concentration chlorine exposure in vivo (500 ppm for 30 min) caused decreased total ATP content and loss of sarcoendoplasmic reticulum calcium ATPase (SERCA) activity. Loss of SERCA activity was attributed to chlorination of tyrosine residues and oxidation of an important cysteine residue, cysteine-674, in SERCA, as demonstrated by immunoblots and mass spectrometry. Using cardiomyocytes, we found that chlorine-induced cell death and damage to SERCA could be decreased by thiocyanate, an important biological antioxidant, and by genetic SERCA2 overexpression. We also investigated a U.S. Food and Drug Administration-approved drug, ranolazine, used in treatment of cardiac diseases, and previously shown to stabilize SERCA in animal models of ischemia-reperfusion. Pretreatment with ranolazine or istaroxime, another SERCA activator, prevented chlorine-induced cardiomyocyte death. Further investigation of responsible mechanisms showed that ranolazine- and istaroxime-treated cells preserved mitochondrial membrane potential and ATP after chlorine exposure. Thus, these studies demonstrate a novel critical target for chlorine in the heart and identify potentially useful therapies to mitigate toxicity of acute chlorine exposure.

  17. Reaction kinetics and transformation of antipyrine chlorination with free chlorine.

    PubMed

    Cai, Mei-Quan; Feng, Li; Jiang, Jin; Qi, Fei; Zhang, Li-Qiu

    2013-05-15

    Chlorine has been documented that it can effectively remove some pharmaceuticals. Recently, new active oxidants chlorine monoxide and molecular chlorine, which exist as free active chlorine in solution, were reported during pharmaceuticals chlorination. In this study, reaction kinetics, active oxidants, and transformation products during antipyrine chlorination were investigated with batch experiments. The reaction orders in [chlorine] were determined at various pH (6.53-7.62) and ranged from 1.13 ± 0.15 to 1.59 ± 0.08, which indicated that antipyrine chlorination is the concurrent existence of reactions appearing first-order and second-order in [chlorine]. The results by varying solution conditions (solution pH, chloride, ionic strength, and buffer concentration) show that chlorine monoxide and molecular chlorine play significant roles during the process of antipyrine chlorination. With kinetics modeling, the second-order rate constants for hypochlorous acid, chlorine monoxide, and molecular chlorine were obtained at 25 ± 2 °C (units: M(-1) s(-1)): kHOCl = 3.23 × 10(3), kCL2 = 2.86 × 10(7), kCL2O= 8.38 × 10(9) (R(2) = 0.9801). At pH 7, hypochlorous acid and chlorine monoxide are the main contributors to the degradation of antipyrine, about 80% and 20%, respectively (calculated by kHOCl, kCL2 and kCL2O. By applying these rate constants to predict the antipyrine elimination in real water matrixes (surface water, ground water), a good agreement was obtained, particularly in ground water. Moreover, liquid chromatography-tandems mass spectrometry (LC-MS/MS) and gas chromatograph-mass spectrometry (GC-MS) were used for products identification. Two main intermediate products and three stable products were observed during the process of antipyrine chlorination. The possible routes for antipyrine chlorination were proposed, which mainly consisted of halogenations, dealkylations and hydroxylations.

  18. Impact of water quality on chlorine demand of corroding copper.

    PubMed

    Lytle, Darren A; Liggett, Jennifer

    2016-04-01

    Copper is widely used in drinking water premise plumbing system materials. In buildings such as hospitals, large and complicated plumbing networks make it difficult to maintain good water quality. Sustaining safe disinfectant residuals throughout a building to protect against waterborne pathogens such as Legionella is particularly challenging since copper and other reactive distribution system materials can exert considerable demands. The objective of this work was to evaluate the impact of pH and orthophosphate on the consumption of free chlorine associated with corroding copper pipes over time. A copper test-loop pilot system was used to control test conditions and systematically meet the study objectives. Chlorine consumption trends attributed to abiotic reactions with copper over time were different for each pH condition tested, and the total amount of chlorine consumed over the test runs increased with increasing pH. Orthophosphate eliminated chlorine consumption trends with elapsed time (i.e., chlorine demand was consistent across entire test runs). Orthophosphate also greatly reduced the total amount of chlorine consumed over the test runs. Interestingly, the total amount of chlorine consumed and the consumption rate were not pH dependent when orthophosphate was present. The findings reflect the complex and competing reactions at the copper pipe wall including corrosion, oxidation of Cu(I) minerals and ions, and possible oxidation of Cu(II) minerals, and the change in chlorine species all as a function of pH. The work has practical applications for maintaining chlorine residuals in premise plumbing drinking water systems including large buildings such as hospitals. PMID:26826646

  19. Application of thermal desorption to the development of a gas chromatographic/mass spectrometric method for the determination of toluene, chlorinated aromatic hydrocarbons, and 2,3,7,8-tetrachlorodibenzo-p-dioxin in combustion emissions.

    PubMed

    Donaldson, John D; Grimes, Susan M; Mehta, Lina; Jafari, Ahmad J

    2003-01-01

    A fast and accurate analytical method, which uses commercially available adsorbents (Tenax TA, Carbotrap B and C, and Carbosieve S-III), was developed for the sampling and determination of aromatic hydrocarbons, chloroaromatic compounds, and 2,3,7,8-tetrachlorodibenzo-p-dioxin. The breakthrough volume data show that Carbotrap C has a good capacity for compounds of high molecular weight, whereas Carbosieve S-III and Tenax TA are efficient for volatile compounds. The organic components are thermally desorbed and transferred to a gas chromatograph/mass spectrometer. Importantly, thermal desorption avoids conventional solvent extraction procedures and also allows reuse of adsorbent tubes. Preliminary results for recovery of analytes from tubes packed with single adsorbent prove that a single-adsorbent bed is not capable of sampling a wide range of compounds. The best method to obtain the desired collection and desorption properties is to use adsorbent tubes containing several different materials. The results of optimization studies are summarized. PMID:12607738

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

    NASA Astrophysics Data System (ADS)

    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. Hydrodesulfurization of chlorinized coal

    NASA Technical Reports Server (NTRS)

    Kalvinskas, J. J.; Rohatgi, N. K. (Inventor)

    1983-01-01

    A method of desulfurization is described in which high sulfur coals are desulfurized by low temperature chlorinolysis of coal in liquid media, preferably water, followed by hydrodesulfurization at a temperature above 500 C. The coals are desulfurized to an extent of up to 90% by weight and simultaneously dechlorinated to a chlorine content below 0.1% by weight. The product coals have lower volatiles loss, lower oxygen and nitrogen content and higher fixed carbon than raw coals treated with hydrogen under the same conditions. Heating the chlorinated coal to a temperature above 500 C. in inert gas such as nitrogen results in significantly less desulfurization.

  2. Condenser targeted chlorination demonstration at Brayton Point Station, Unit 2

    SciTech Connect

    Not Available

    1991-02-01

    EPRI sponsored the development of condenser targeted chlorination to control slime fouling on condenser tubes. Hydraulic model studies, chlorine schedules optimization, and corrosion studies were conducted between 1983 and 1986 to develop design parameters. A full-scale demonstration at the Brayton Point Station -- Unit 2 condenser was performed in 1987--1988. One half of the condenser bundle was fitted with a fixed nozzle targeted injection system. The other half was used as a control with conventional chlorination. The condenser was instrumented to allow daily trending of the cleanliness factors in the targeted and conventionally treated bundles. The chemical parameters, such as the chlorine schedules (dosage, duration, and frequency) and water quality, were documented. The Trihalomethane (THM) levels at the effluent were evaluated and, after the test, tube scrapings were analyzed. Targeted chlorination resulted in: up to 20 percent condenser performance improvement; up to 80 percent chlorine consumption reduction; less than 0.1 ppM total residual chlorine achieved at the effluent in the sealpit; no measurable condenser corrosion; and undetectable levels of THM at the effluent in the sealpit.

  3. EFFECT OF THE DECHLORINATING AGENT, ASCORBIC ACID, ON THE MUTAGENICITY OF CHLORINATED WATER SAMPLES

    EPA Science Inventory

    XAD resin adsorption has been widely used to concentrate the organic compounds present in chlorinated drinking waters prior to mutagenicity testing. Previous work has shown that mutagenic artifcats can arise due to the reaction of residual chlorine with the resins. Althrough the ...

  4. In vitro cytotoxicity of polycyclic aromatic hydrocarbon residues arising through repeated fish fried oil in human hepatoma Hep G2 cell line.

    PubMed

    Pandey, Manoj K; Pant, Aditya B; Das, Mukul

    2006-04-01

    Repeated frying of vegetarian and non-vegetarian foods in edible oil is a common practice round the globe. Our studies suggest that repeated fish fried oil (RFFO) generates polycyclic aromatic hydrocarbons (PAHs), which may lead to hazardous effect on human health. In order to understand the mechanism of toxicity of RFFO extracts containing a mixture of PAHs, the in vitro cytotoxicity assays in human hepatoma cell line, Hep G2 was undertaken. In addition to RFFO extract, benzo(a)pyrene (BP) and chrysene were used as prototype compounds for heavy and light PAHs, respectively. Doses of BP and chrysene were made in such a way, that it could represent the appropriate content of heavy and light PAHs found in the RFFO extract. Out of total content of PAHs (1240.4 microg/kg) in RFFO, major composition is of light PAHs (854.8 microg/kg) while heavy PAHs showed the concentration of 385.7 microg/kg. Treatment of cells with 1 microg/ml RFFO extract for 48 h showed significant induction in ethoxyresorufin-O-deethylase (EROD) activity. Exposure of cells to higher doses of RFFO extract (10-100 microg/ml) for 24, 48 and 72 h caused 3.5-5.2, 4.3-8.5 and 1.8-2.3-fold enhancement in EROD activity, respectively. Further, RFFO extract caused a dose dependent increase (2.1-3.5-fold) in aryl hydrocarbon hydroxylase (AHH) activity at 48 h. Induction of EROD and AHH activity in Hep G2 cells was found to be relatively more following BP or chrysene treatment as compared to RFFO extract. RFFO extract did not cause any significant effect on cell viability at 1 microg/ml and 10 microg/ml. However, at 100 microg/ml concentration RFFO extract significantly decreased the cell viability at 24, 48 and 72 h. Exposure of 10 microg/ml RFFO extract reduced the colony forming ability (CFA) of Hep G2 cells with maximum decrease of 33.5% at 72 h. However, exposure of cells to RFFO extract at highest concentration of assay (100 microg/ml) reduced CFA (35-52%) at 24, 48 and 72 h. RFFO extract (1-100 microg

  5. Chlorine dioxide and hemodialysis

    SciTech Connect

    Smith, R.P. . Dept. of Pharmacology and Toxicology)

    1989-05-01

    Because it has little or no tendency to generate carcinogenic trihalomethanes such as chloroform, chlorine dioxide is an attractive alternative to chlorine for drinking water disinfection. There are, however, concerns about its acute toxicity, and the toxic effects of its by-products, chlorite and chlorate. The human experience with chlorine dioxide in both controlled, prospective studies and in actual use situations in community water supplies have as yet failed to reveal adverse health effects. The EPA has recommended standards of 0.06 mg/L for chlorine dioxide and standards of 0.007 mg/L for chlorite and chlorate in drinking water. Among groups who may be at special risk from oxychlorines in drinking water are patients who must undergro chronic extracorporeal hemodialysis. Although even units for home hemodialysis are supposed to be equipped with devices which effectively remove oxychlorines, there is a always a possibility of operator error or equipment failure. When the equipment is adequately maintained, it is likely that dialysis patients will have more intensive exposures from drinking water than from dialysis fluids despite the much larger volumes of water that are involved in dialysis. This paper discusses a hemodialysis and the standards and effects of oxychlorines. 90 refs., 2 tabs.

  6. Chlorination of lanthanum oxide.

    PubMed

    Gaviría, Juan P; Navarro, Lucas G; Bohé, Ana E

    2012-03-01

    The reactive system La(2)O(3)(s)-Cl(2)(g) was studied in the temperature range 260-950 °C. The reaction course was followed by thermogravimetry, and the solids involved were characterized by X-ray diffraction, scanning electron microscopy, and energy dispersive spectroscopy. The results showed that the reaction leads to the formation of solid LaOCl, and for temperatures above 850 °C, the lanthanum oxychloride is chlorinated, producing LaCl(3)(l). The formation of the oxychloride progresses through a nucleation and growth mechanism, and the kinetic analysis showed that at temperatures below 325 °C the system is under chemical control. The influence of diffusive processes on the kinetics of production of LaOCl was evaluated by studying the effect of the reactive gas flow rate, the mass of the sample, and the chlorine diffusion through the boundary layer surrounding the solid sample. The conversion curves were analyzed and fitted according to the Johnson-Mehl-Avrami description, and the reaction order with respect to the chlorine partial pressure was obtained by varying this partial pressure between 10 and 70 kPa. The rate equation was obtained, which includes the influence of the temperature, chlorine partial pressure, and reaction degree.

  7. Chlorine Dioxide (Gas)

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Chlorine dioxide (ClO2) gas is registered by the U.S. Environmental Protection Agency (EPA) as a sterilant for use in manufacturing, laboratory equipment, medical devices, environmental surfaces, tools and clean rooms. Aqueous ClO2 is registered by the EPA as a surface disinfectant and sanitizer fo...

  8. Impacts of Water Chlorination

    ERIC Educational Resources Information Center

    Environmental Science and Technology, 1976

    1976-01-01

    To learn the consequences of one aspect of technology on man and his surroundings, scientists meeting at the Oak Ridge National Laboratory discussed what is known about the impacts of water chlorination. The conference produced state-of-the-art information about the technology and attempted to summarize all the information on the subject. (BT)

  9. Chlorination of lanthanum oxide.

    PubMed

    Gaviría, Juan P; Navarro, Lucas G; Bohé, Ana E

    2012-03-01

    The reactive system La(2)O(3)(s)-Cl(2)(g) was studied in the temperature range 260-950 °C. The reaction course was followed by thermogravimetry, and the solids involved were characterized by X-ray diffraction, scanning electron microscopy, and energy dispersive spectroscopy. The results showed that the reaction leads to the formation of solid LaOCl, and for temperatures above 850 °C, the lanthanum oxychloride is chlorinated, producing LaCl(3)(l). The formation of the oxychloride progresses through a nucleation and growth mechanism, and the kinetic analysis showed that at temperatures below 325 °C the system is under chemical control. The influence of diffusive processes on the kinetics of production of LaOCl was evaluated by studying the effect of the reactive gas flow rate, the mass of the sample, and the chlorine diffusion through the boundary layer surrounding the solid sample. The conversion curves were analyzed and fitted according to the Johnson-Mehl-Avrami description, and the reaction order with respect to the chlorine partial pressure was obtained by varying this partial pressure between 10 and 70 kPa. The rate equation was obtained, which includes the influence of the temperature, chlorine partial pressure, and reaction degree. PMID:22280490

  10. The historical residue trends of DDT, hexachlorocyclohexanes and polycyclic aromatic hydrocarbons in an ice core from Mt. Everest, central Himalayas, China

    NASA Astrophysics Data System (ADS)

    Wang, Xiao ping; Xu, Bai qing; Kang, Shi chang; Cong, Zhi yuan; Yao, Tan dong

    High mountains may serve as "cold traps" for persistent organic pollutants (POPs) and ice cores can provide long-term records of atmospheric deposition of pollutants. In this study, DDT, hexachlorocyclohexanes (HCHs) and polycyclic aromatic hydrocarbons (PAHs) in an ice core from East Rongbuk Glacier were analyzed and the deposition fluxes of these pollutants were investigated. Concentrations of total DDTs reached maxima of approximately 2 ng l -1 in mid-1970s, which is corresponding to the peak of malaria cases in India (in 1976). The decrease of DDT concentration after 1990s was in-line with the ban of DDT in India (in 1989). High level of α-HCH was observed in early 1970s and it showed a decrease to undetectable level at the end of 1990s, which is in agreement with the period when India banned the usage of HCH (in 1997). Concentrations of total PAHs sharply increased after 1990 and the peak (approximately 100 ng l -1) was found at the end of 1990s, when India entered the rapid industrialization (urbanization). PAHs in the ice core are dominantly pyrogenic in source, and are mainly from incomplete combustion of coal and biomass burning. Good correlations among concentrations of PAHs, nssSO 42- and microparticles in snow pit samples showed that the origin of the PAHs and nssSO 42- is often the same and they may be absorbed by particles and transported to high mountain regions by atmospheric circulation.

  11. Characterisation of polycyclic aromatic hydrocarbons in flue gas and residues of a full scale fluidized bed combustor combusting non-hazardous industrial waste.

    PubMed

    Van Caneghem, J; Vandecasteele, C

    2014-11-01

    This paper studies the fate of PAHs in full scale incinerators by analysing the concentration of the 16 EPA-PAHs in both the input waste and all the outputs of a full scale Fluidized Bed Combustor (FBC). Of the analysed waste inputs i.e. Waste Water Treatment (WWT) sludge, Refuse Derived Fuel (RDF) and Automotive Shredder Residue (ASR), RDF and ASR were the main PAH sources, with phenanthrene, fluoranthene and pyrene being the most important PAHs. In the flue gas sampled at the stack, naphthalene was the only predominant PAH, indicating that the PAHs in FBC's combustion gas were newly formed and did not remain from the input waste. Of the other outputs, the boiler and fly ash contained no detectable levels of PAHs, whereas the flue gas cleaning residue contained only low concentrations of naphthalene, probably adsorbed from the flue gas. The PAH fingerprint of the bottom ash corresponded rather well to the PAH fingerprint of the RDF and ASR, indicating that the PAHs in this output, in contrast to the other outputs, were mainly remainders from the PAHs in the waste inputs. A PAH mass balance showed that the total PAH input/output ratio of the FBC ranged from about 100 to about 2600 depending on the waste input composition and the obtained combustion conditions. In all cases, the FBC was clearly a net PAH sink. PMID:25002370

  12. Characterisation of polycyclic aromatic hydrocarbons in flue gas and residues of a full scale fluidized bed combustor combusting non-hazardous industrial waste.

    PubMed

    Van Caneghem, J; Vandecasteele, C

    2014-11-01

    This paper studies the fate of PAHs in full scale incinerators by analysing the concentration of the 16 EPA-PAHs in both the input waste and all the outputs of a full scale Fluidized Bed Combustor (FBC). Of the analysed waste inputs i.e. Waste Water Treatment (WWT) sludge, Refuse Derived Fuel (RDF) and Automotive Shredder Residue (ASR), RDF and ASR were the main PAH sources, with phenanthrene, fluoranthene and pyrene being the most important PAHs. In the flue gas sampled at the stack, naphthalene was the only predominant PAH, indicating that the PAHs in FBC's combustion gas were newly formed and did not remain from the input waste. Of the other outputs, the boiler and fly ash contained no detectable levels of PAHs, whereas the flue gas cleaning residue contained only low concentrations of naphthalene, probably adsorbed from the flue gas. The PAH fingerprint of the bottom ash corresponded rather well to the PAH fingerprint of the RDF and ASR, indicating that the PAHs in this output, in contrast to the other outputs, were mainly remainders from the PAHs in the waste inputs. A PAH mass balance showed that the total PAH input/output ratio of the FBC ranged from about 100 to about 2600 depending on the waste input composition and the obtained combustion conditions. In all cases, the FBC was clearly a net PAH sink.

  13. Avoidance responses of estuarine fish subjected to heated chlorinated and dechlorinated power plant effluents

    SciTech Connect

    Not Available

    1983-12-01

    The avoidance responses of striped bass (Morone saxatilis) and Atlantic menhaden (Brevoortia tyrannus) exposed to simultaneous total residual chlorine (TRC) and dechlorinated conditions were evaluated at acclimation temperatures of 15, 20, 25 and 30C.

  14. PCB removal by conventional water treatment: effect of chemical coagulation and chlorination

    SciTech Connect

    Aly, O.A.; Badawy, M.I.

    1986-06-01

    Previous studies revealed that residue levels of PCBs in the drinking waters in Egypt tend to exceed the permissible levels. This study evaluated the efficiency of coagulation and chlorination for removal of PCBs from drinking water.

  15. Snapping Turtles (Chelydra serpentina) from Canadian Areas of Concern across the southern Laurentian Great Lakes: Chlorinated and brominated hydrocarbon contaminants and metabolites in relation to circulating concentrations of thyroxine and vitamin A.

    PubMed

    Letcher, Robert J; Lu, Zhe; de Solla, Shane R; Sandau, Courtney D; Fernie, Kimberly J

    2015-11-01

    The metabolites of polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs), as well as other halogenated phenolic contaminants (HPCs) have been shown to have endocrine-disrupting properties, and have been reported with increasing frequency in the blood of wildlife, and mainly in mammals and birds. However, little is known about the persistence, accumulation and distribution of these contaminants in long-lived freshwater reptiles. In the present study, in addition to a large suite of chlorinated and brominated contaminants, metabolites and HPCs, we assessed and compared hydroxylated (OH) PCBs and OH-PBDEs relative to PCBs and PBDEs, respectively, in the plasma of adult male common snapping turtles (Chelydra serpentina). Blood samples were collected from 62 snapping turtles (2001-2004) at 12 wetland sites between the Detroit River and the St. Lawrence River on the Canadian side of the Laurentian Great Lakes of North America. Turtles were sampled from sites designated as Areas of Concern (AOCs) and from a relatively clean reference site in southern Georgian Bay (Tiny Marsh), Lake Huron. Plasma concentrations of Σ46PCB (10-340 ng/g wet weight (ww)) and Σ28OH-PCB (3-83 ng/g ww) were significantly greater (p<0.05) in turtles from the Turkey Creek and Muddy Creek-Wheatley Harbour sites in Lake Erie compared with the reference site turtles. The HPC, pentachlorophenol (PCP), had a mean concentration of 9.6±1.1 ng/g ww. Of the 28 OH-CB congeners screened for, 4-OH-CB187 (42±7 ng/g ww) was the most concentrated of all HPCs measured. Of the 14 OH-BDE congeners examined, four (4'-OH-BDE17, 3-OH-BDE47, 5-OH-BDE47 and 4'-OH-BDE49) were consistently found in all plasma samples. p,p'-DDE was the most concentrated of the 18 organochlorine pesticides (OCPs) examined. The mean concentrations of circulating total thyroxine (TT4), dehydroretinol and retinol in the plasma of the male snapping turtles regardless of sampling site were 5.4±0.3, 81±4.7 and 291±13

  16. Snapping Turtles (Chelydra serpentina) from Canadian Areas of Concern across the southern Laurentian Great Lakes: Chlorinated and brominated hydrocarbon contaminants and metabolites in relation to circulating concentrations of thyroxine and vitamin A.

    PubMed

    Letcher, Robert J; Lu, Zhe; de Solla, Shane R; Sandau, Courtney D; Fernie, Kimberly J

    2015-11-01

    The metabolites of polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs), as well as other halogenated phenolic contaminants (HPCs) have been shown to have endocrine-disrupting properties, and have been reported with increasing frequency in the blood of wildlife, and mainly in mammals and birds. However, little is known about the persistence, accumulation and distribution of these contaminants in long-lived freshwater reptiles. In the present study, in addition to a large suite of chlorinated and brominated contaminants, metabolites and HPCs, we assessed and compared hydroxylated (OH) PCBs and OH-PBDEs relative to PCBs and PBDEs, respectively, in the plasma of adult male common snapping turtles (Chelydra serpentina). Blood samples were collected from 62 snapping turtles (2001-2004) at 12 wetland sites between the Detroit River and the St. Lawrence River on the Canadian side of the Laurentian Great Lakes of North America. Turtles were sampled from sites designated as Areas of Concern (AOCs) and from a relatively clean reference site in southern Georgian Bay (Tiny Marsh), Lake Huron. Plasma concentrations of Σ46PCB (10-340 ng/g wet weight (ww)) and Σ28OH-PCB (3-83 ng/g ww) were significantly greater (p<0.05) in turtles from the Turkey Creek and Muddy Creek-Wheatley Harbour sites in Lake Erie compared with the reference site turtles. The HPC, pentachlorophenol (PCP), had a mean concentration of 9.6±1.1 ng/g ww. Of the 28 OH-CB congeners screened for, 4-OH-CB187 (42±7 ng/g ww) was the most concentrated of all HPCs measured. Of the 14 OH-BDE congeners examined, four (4'-OH-BDE17, 3-OH-BDE47, 5-OH-BDE47 and 4'-OH-BDE49) were consistently found in all plasma samples. p,p'-DDE was the most concentrated of the 18 organochlorine pesticides (OCPs) examined. The mean concentrations of circulating total thyroxine (TT4), dehydroretinol and retinol in the plasma of the male snapping turtles regardless of sampling site were 5.4±0.3, 81±4.7 and 291±13

  17. Environmental availability of chlorinated organics, explosives, and metals in soils

    SciTech Connect

    Anderson, W.C.; Loehr, R.C.; Smith, B.P.

    1999-08-01

    Environmental availability is key to defining the extent of remediation required. Nationally recognized experts summarize what is known about the environmental availability of chlorinated organics (Perry McCarty), explosives (Judith Pennington), and metals (Rufus Chaney). It also summarizes the current use of environmental availability to set cleanup goals for petroleum hydrocarbons and identifies essential research needed to expand the knowledge base for environmental availability.

  18. Distribution of chlorine in coal

    SciTech Connect

    Zhao Fenghua; Ren Deyi; Zhang Shuangquan; Zhang Wang

    1998-12-31

    The current advance of study on chlorine in coal is reviewed. The concentrations of chlorine in 45 Chinese coal samples are determined on whole coal basis using instrumental neutron activation analysis (INAA). The sequential chemical extraction method is put forward to determine the occurrence modes of chlorine in coal. The research shows that Chinese coals are not chlorine-rich ones compared with those from other countries. In coal from Pingshuo Antaibao Opencast Mine, 46.70%--91.78% of chlorine is in a water-soluble state, 5.20%--48.38% of it is organic chlorine bonded to coal molecules, and only 4.92%--18.78% is an organic one in an ion-exchange state; the proportions of organic chlorine increase with the decrease in ash of coal.

  19. Chlorine Analysis - Wastewater. Training Module 5.125.2.77.

    ERIC Educational Resources Information Center

    Kirkwood Community Coll., Cedar Rapids, IA.

    This document is an instructional module package prepared in objective form for use by an instructor familiar with the laboratory procedures for determining the combined chlorine residual of a wastewater sample. Included are objectives, instructor guides, student handouts, and transparency masters. This module considers the amperometric, DPD,…

  20. Chlorofluorocarbon CFCs, potential alternative HCFCs and HFCs, and related chlorinated compounds: mass spectral study, Part II.

    PubMed

    Reizian-Fouley, A; Dat, Y; Rault, S

    1997-04-01

    In a previous publication, mass spectrometry was applied to the study of several ions formed by dissociative ionization of ethanes, partially substituted with fluorine and chlorine, and to the determination of the fragmentation pattern of each related compound. The aim of the present investigation was to extend this mass spectral study (70 eV and low ionization energy) to a group of closely related analogs, hydrofluorocarbons (HCFCs), HFCs, chlorinated fluorocarbons, and chlorinated hydrocarbons--halogenated methane, ethane, and propane molecules--to make an attempt to predict the relative bond strength and then the behavior--metabolic pathway and tropospheric degradation--of new HCFCs and HFCs.

  1. Performance and reliability improvement of HfSiON gate dielectrics using chlorine plasma treatment

    SciTech Connect

    Park, Hong Bae; Ju, Byongsun; Kang, Chang Yong; Park, Chanro; Park, Chang Seo; Lee, Byoung Hun; Kim, Tea Wan; Kim, Beom Seok; Choi, Rino

    2009-01-26

    The effects of chlorine plasma treatment on HfSiON gate dielectrics were investigated with respect to device performance and reliability characteristics. The chlorine plasma treatment was performed on atomic layer deposited HfSiON films to remove the residual carbon content. The optimal chlorine plasma treatment is shown to lower gate leakage current density without increasing equivalent oxide thickness of the gate stack. Secondary ion mass spectroscopy depth profiling showed that the carbon residue in HfSiON was reduced by the chlorine plasma treatment. It is demonstrated that an optimized chlorine plasma treatment improves the transistor I{sub on}-I{sub off} characteristics and reduces negative-bias temperature instability.

  2. Performance of chlorination process during nanofiltration of sulfonamide antibiotic.

    PubMed

    Ramli, Mohd Redzuan; Sulaiman, Nik Meriam Nik; Mohd, Mustafa Ali; Rabuni, Mohamad Fairus

    2015-01-01

    The effectiveness of combined nanofiltration and disinfection processes was studied by comparing the pre-disinfection and post-disinfection when in combination with nanofiltration. Four types of sulfonamide (sulfanilamide, sulfadiazine, sulfamethoxazole, and sulfadimethoxine) were chosen as substrates, with sodium hypochlorite as a disinfectant. A laboratory-scale nanofiltration system was used to conduct the following sets of experiment: (1) a pre-chlorination system, where the free active chlorine (FAC) was added to the membrane influent; and (2), a post-chlorination system, where the FAC was added to the membrane effluent. Overall, the pre-disinfection nanofiltration system showed higher sulfonamide removal efficiency compared to the post-chlorination nanofiltration system (>99.5% versus >89.5%). In the case of limited FAC ([FAC]0: [sulfonamide]0≤1), the removal efficiency for the post-chlorination nanofiltration system was higher, due to the prior nanofiltration process that could remove 12.5% to 80% of sulfonamide. The flux of the treated feed system was considerably higher than in the untreated feed system; however, the membrane was observed to be slightly damaged due to residual chlorine attack. PMID:26524453

  3. Bacterial repopulation of drinking water pipe walls after chlorination.

    PubMed

    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

  4. Bacterial repopulation of drinking water pipe walls after chlorination.

    PubMed

    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.

  5. Lethality of chlorine, chlorine dioxide, and a commercial produce sanitizer to Bacillus cereus and Pseudomonas in a liquid detergent, on stainless steel, and in biofilm.

    PubMed

    Kreske, Audrey C; Ryu, Jee-Hoon; Pettigrew, Charles A; Beuchat, Larry R

    2006-11-01

    Many factors that are not fully understood may influence the effectiveness of sanitizer treatments for eliminating pathogens and spoilage microorganisms in food or detergent residues or in biofilms on food contact surfaces. This study was done to determine the sensitivities of Pseudomonas cells and Bacillus cereus cells and spores suspended in a liquid dishwashing detergent and inoculated onto the surface of stainless steel to treatment with chlorine, chlorine dioxide, and a commercial produce sanitizer (Fit). Cells and spores were incubated in a liquid dishwashing detergent for 16 to 18 h before treatment with sanitizers. At 50 microg/ml, chlorine dioxide killed a significantly higher number of Pseudomonas cells (3.82 log CFU/ml) than did chlorine (a reduction of 1.34 log CFU/ml). Stainless steel coupons were spot inoculated with Pseudomonas cells and B. cereus cells and spores, with water and 5% horse serum as carriers. Chlorine was more effective than chlorine dioxide in killing cells and spores of B. cereus suspended in horse serum. B. cereus biofilm on stainless steel coupons that were treated with chlorine dioxide or chlorine at 200 microg/ml had total population reductions (vegetative cells plus spores) of > or = 4.42 log CFU per coupon; the number of spores was reduced by > or = 3.80 log CFU per coupon. Fit (0.5%) was ineffective for killing spot-inoculated B. cereus and B. cereus in biofilm, but treatment with mixtures of Fit and chlorine dioxide caused greater reductions than did treatment with chlorine dioxide alone. In contrast, when chlorine was combined with Fit, the lethality of chlorine was completely lost. This study provides information on the survival and sanitizer sensitivity of Pseudomonas and B. cereus in a liquid dishwashing detergent, on the surface of stainless steel, and in a biofilm. This information will be useful for developing more effective strategies for cleaning and sanitizing contact surfaces in food preparation and processing

  6. Effectiveness of breakpoint chlorination to reduce accelerated chemical chloramine decay in severely nitrified bulk waters.

    PubMed

    Bal Krishna, K C; Sathasivan, Arumugam; Kastl, George

    2014-12-01

    Rectifying the accelerated chloramine decay after the onset of nitrification is a major challenge for water utilities that employ chloramine as a disinfectant. Recently, the evidence of soluble microbial products (SMPs) accelerating chloramine decay beyond traditionally known means was reported. After the onset of nitrification, with an intention to inactivate nitrifying bacteria and thus maintaining disinfectant residuals, breakpoint chlorination followed by re-chloramination is usually practiced by water utilities. However, what actually breakpoint chlorination does beyond known effects is not known, especially in light of the new finding of SMPs. In this study, experiments were conducted using severely nitrified chloraminated water samples (chloramine residuals <0.5 mg Cl2 L−1, nitrite residuals >0.1 mg N L−1 and an order of magnitude higher chloramine decay rate compared to normal decay) obtained from two laboratory scale systems operated by feeding natural organic matter (NOM) containing and NOM free waters. Results showed that the accelerated decay of chloramine as a result of SMPs can be eliminated by spiking higher free chlorine residuals (about 0.92 ± 0.03 to 1.16 ± 0.12 mg Cl2 L−1) than the stoichiometric requirement for breakpoint chlorination and nitrite oxidation. Further, accelerated initial chlorine decay showed chlorine preferentially reacts with nitrite and ammonia before destroying SMPs. This study, clearly demonstrated there is an additional demand from SMPs that needs to be satisfied to effectively recover disinfection residuals in subsequent re-chloramination. PMID:25461936

  7. Process for converting light alkanes to higher hydrocarbons

    DOEpatents

    Noceti, Richard P.; Taylor, Charles E.

    1988-01-01

    A process is disclosed for the production of aromatic-rich, gasoline boiling range hydrocarbons from the lower alkanes, particularly from methane. The process is carried out in two stages. In the first, alkane is reacted with oxygen and hydrogen chloride over an oxyhydrochlorination catalyst such as copper chloride with minor proportions of potassium chloride and rare earth chloride. This produces an intermediate gaseous mixture containing water and chlorinated alkanes. The chlorinated alkanes are contacted with a crystalline aluminosilicate catalyst in the hydrogen or metal promoted form to produce gasoline range hydrocarbons with a high proportion of aromatics and a small percentage of light hydrocarbons (C.sub.2 -C.sub.4). The light hydrocarbons can be recycled for further processing over the oxyhydrochlorination catalyst.

  8. 40 CFR 704.43 - Chlorinated naphthalenes.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... § 704.43 Chlorinated naphthalenes. (a) Definitions—(1) Extent of chlorination means the percent by... the chlorine atom(s) on the naphthalene. (4) Polychlorinated biphenyl means any chemical...

  9. 21 CFR 177.1610 - Polyethylene, chlorinated.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... chlorinated polyethylene contains a maximum of 60 percent by weight of total chlorine, as determined by ASTM 1method D1303-55 (Reapproved 1979), “Standard Test Method for Total Chlorine in Vinyl Chloride...

  10. Basic Gas Chlorination Workshop Manual.

    ERIC Educational Resources Information Center

    Ontario Ministry of the Environment, Toronto.

    This manual was developed for use at workshops designed to introduce treatment plant operators to the safe operation and maintenance of gas chlorination systems employing the variable vacuum gas chlorinator. Each of the lessons in this document has clearly stated behavioral objectives to tell the trainee what he should know or do after completing…

  11. Papillomas on fish exposed to chlorinated wastewater effluent.

    PubMed

    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

  12. Site remediation using photocatalytic VOC destruction of chlorinated hydrocarbons

    SciTech Connect

    Brunet, R.A.H.; Pearcey, R.; Kittrell, J.R.; Mackin, G.; Wise, C.A.

    1999-07-01

    An innovative environmental technology has been developed and demonstrated for cost-effective control of toxic air emissions, such as trichloroethylene (TCE) and perchloroethylene (PCE), found in soil and groundwater at hazardous waste sites and in industrial effluents. The technology uses UV light and a proprietary photocatalyst to adsorb and destroy pollutants at ambient conditions, even with high humidity. Air stripping and soil vapor extraction efficiently transfer the pollutants to the gas phase, where they can be economically treated by photocatalysis without the risk of hazardous by-product formation. The AIR2000 photocatalytic technology was successfully installed at the Stamina Mills Superfund site in Rhode Island, where a commercial scale unit is treating 700 cfm of up to 1,000 ppm TCE, mixed with PCE, dichloroethylene (DCE), trichloroethane (TCA), and vinyl chloride (VC) produced through a combination of soil vapor extraction (SVE) and air stripping. As part of the EPA SITE program, the system was monitored for overall destruction removal efficiency (DRE) and hazardous by-product formation. A DRE in excess of 99% was reported over the first four months of operation, with greater than 99.99% DRE achieved, without production of hazardous by-products. The operating cost of the system is approximately 20% of activated carbon adsorption, which provides approximately $1,500,000 in cost savings over the life of the Stamina Mills project. The Adsorption Integrated Reaction (AIR) process is the recipient of the 1997 SBIR Technology of the Year award, the 1998 EPA Environmental Technology Innovator Award, and the 1998 R and D 100 Award.

  13. Chlorinated hydrocarbons in the young of Lake Michigan coho salmon

    USGS Publications Warehouse

    Willford, W.A.; Sills, J.B.; Whealdon, E.W.

    1969-01-01

    Three thousand eyed coho salmon (Oncorhynchus kisutch) eggs from Lake Michigan stock were sent by the Department of Natural Resources to the Fish Control Laboratory, La Crosse, Wis., on January 15, 1969, for use in evaluating candidate fish-cnotrol chemicals.

  14. Biological Chlorine Cycling in Arctic Peat Soils

    NASA Astrophysics Data System (ADS)

    Zlamal, J. E.; Raab, T. K.; Lipson, D.

    2014-12-01

    Soils of the Arctic tundra near Barrow, Alaska are waterlogged and anoxic throughout most of the profile due to underlying permafrost. Microbial communities in these soils are adapted for the dominant anaerobic conditions and are capable of a surprising diversity of metabolic pathways. Anaerobic respiration in this environment warrants further study, particularly in the realm of electron cycling involving chlorine, which preliminary data suggest may play an important role in arctic anaerobic soil respiration. For decades, Cl was rarely studied outside of the context of solvent-contaminated sites due to the widely held belief that it is an inert element. However, Cl has increasingly become recognized as a metabolic player in microbial communities and soil cycling processes. Organic chlorinated compounds (Clorg) can be made by various organisms and used metabolically by others, such as serving as electron acceptors for microbes performing organohalide respiration. Sequencing our arctic soil samples has uncovered multiple genera of microorganisms capable of participating in many Cl-cycling processes including organohalide respiration, chlorinated hydrocarbon degradation, and perchlorate reduction. Metagenomic analysis of these soils has revealed genes for key enzymes of Cl-related metabolic processes such as dehalogenases and haloperoxidases, and close matches to genomes of known organohalide respiring microorganisms from the Dehalococcoides, Dechloromonas, Carboxydothermus, and Anaeromyxobacter genera. A TOX-100 Chlorine Analyzer was used to quantify total Cl in arctic soils, and these data were examined further to separate levels of inorganic Cl compounds and Clorg. Levels of Clorg increased with soil organic matter content, although total Cl levels lack this trend. X-ray Absorption Near Edge Structure (XANES) was used to provide information on the structure of Clorg in arctic soils, showing great diversity with Cl bound to both aromatic and alkyl groups

  15. Chlorination byproducts, their toxicodynamics and removal from drinking water.

    PubMed

    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.

  16. Apparatus for hydrocarbon extraction

    SciTech Connect

    Bohnert, George W.; Verhulst, Galen G.

    2013-03-19

    Systems and methods for hydrocarbon extraction from hydrocarbon-containing material. Such systems and methods relate to extracting hydrocarbon from hydrocarbon-containing material employing a non-aqueous extractant. Additionally, such systems and methods relate to recovering and reusing non-aqueous extractant employed for extracting hydrocarbon from hydrocarbon-containing material.

  17. Perspectives on the Meaning of Detectable Distribution System Residual and Implications for N. Fowleri Control

    EPA Science Inventory

    The objectives of this presentation are to: review history of distribution system chlorination regulations, raise awareness on the meaning of detectable residual as it relates to chloramines, and perhaps renew dialogue on the discussion of minimum disinfectant residuals.

  18. Chlorination/dechlorination studies relating to proposed cooling towers for K and C reactors

    SciTech Connect

    Wilde, E.W.

    1986-12-01

    The purpose of this study was to obtain data on the chlorination and dechlorination of the cooling water that is pumped through the C- and K-Reactor heat exchangers. More specifically, data were obtained on: (1) chlorine demand and dissipation rates; (2) the effectiveness of sodium sulfite as a dechlorinating agent; (3) the toxicity of chlorination and dechlorination on indigenous fish; (4) the effects of dechlorination on water quality; and (5) the comparative precision of three conventional residual chlorine detection methods. The study results strongly indicate that implementation of present plans for chlorination and dechlorination (with sodium sulfite) of SRP reactor cooling towers will cause no significant adverse environmental impacts and should not result in problems in meeting future regulatory guidelines for TRC. 9 figs., 11 tabs.

  19. Zebra mussel mortality with chlorine

    SciTech Connect

    Van Benschoten, J.E.; Jensen, J.N.; Harrington, D.; DeGirolamo, D.J.

    1995-05-01

    The rate of mortality of the zebra mussel in response to chlorine is described by a kinetic model that combines a statistical characterization of mussel mortality with a disinfection-type modeling approach. Parameter estimates were made with nine sets of data from experiments conducted in Niagara River water. From the kinetic model, an operational diagram was constructed that describes the time to 95% mortality as a function of chlorine concentration and temperature. Either the model or the diagram can be used to assist utilities in planning chlorination treatments for controlling zebra mussels.

  20. 46 CFR 151.50-31 - Chlorine.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 46 Shipping 5 2013-10-01 2013-10-01 false Chlorine. 151.50-31 Section 151.50-31 Shipping COAST... LIQUID HAZARDOUS MATERIAL CARGOES Special Requirements § 151.50-31 Chlorine. (a) Chlorine barges. Subparts 98.03 and 98.20 of Part 98 of this chapter have been revoked. However, chlorine barges that...

  1. 46 CFR 151.50-31 - Chlorine.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 46 Shipping 5 2014-10-01 2014-10-01 false Chlorine. 151.50-31 Section 151.50-31 Shipping COAST... LIQUID HAZARDOUS MATERIAL CARGOES Special Requirements § 151.50-31 Chlorine. (a) Chlorine barges. Subparts 98.03 and 98.20 of Part 98 of this chapter have been revoked. However, chlorine barges that...

  2. 21 CFR 177.1610 - Polyethylene, chlorinated.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyethylene, chlorinated. 177.1610 Section 177... Components of Single and Repeated Use Food Contact Surfaces § 177.1610 Polyethylene, chlorinated. Chlorinated... this section. (a) For the purpose of this section, chlorinated polyethylene consists of basic...

  3. 21 CFR 177.1610 - Polyethylene, chlorinated.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyethylene, chlorinated. 177.1610 Section 177... Components of Single and Repeated Use Food Contact Surfaces § 177.1610 Polyethylene, chlorinated. Chlorinated... this section. (a) For the purpose of this section, chlorinated polyethylene consists of basic...

  4. 40 CFR 704.43 - Chlorinated naphthalenes.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Chlorinated naphthalenes. 704.43... § 704.43 Chlorinated naphthalenes. (a) Definitions. (1) Extent of chlorination means the percent by... means the relative amounts of each isomeric chlorinated naphthalene that composes the chemical...

  5. 40 CFR 704.43 - Chlorinated naphthalenes.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Chlorinated naphthalenes. 704.43... § 704.43 Chlorinated naphthalenes. (a) Definitions. (1) Extent of chlorination means the percent by... means the relative amounts of each isomeric chlorinated naphthalene that composes the chemical...

  6. Stimulation of 2-methylisoborneol (MIB) production by actinomycetes after cyclic chlorination in drinking water distribution systems.

    PubMed

    Abbaszadegan, Morteza; Yi, Min; Alum, Absar

    2015-01-01

    The impact of fluctuation in chlorine residual on actinomycetes and the production of 2-methylisoborneol (MIB) were studied in cast-iron and PVC model distribution systems. Actinomycetes were spiked in each system and continued operation for a 12-day non-chlorine experiment, resulting in no changes in actinomycetes and MIB concentrations. Three cyclic chlorination events were performed and chlorine residuals were maintained as follows: 1.0 mg L(-1) for 24 h, 0 mg L(-1) for 48 h, 0.5 mg L(-1) for 48 h, 0 mg L(-1) for 48 h and 2 mg L(-1) for 24 h. After each chlorination event, 2 -3 log decrease in actinomycetes was noted in both systems. However, within 48 h at 0 mg L(-1) chlorine, the actinomycetes recovered to the pre-chlorination levels. On the contrary, MIB concentration in both systems remained un-impacted after the first cycle and increased by fourfold (< 5 to > 20 mg L(-1)) after the second cycle, which lasted through the third cycle despite the fact that actinomycetes numbers fluctuated 2-3 logs during this time period. For obtaining biofilm samples from field, water meters were collected from municipality drinking water distribution systems located in central Arizona. The actinomycetes concentration in asbestos cement pipe and cast iron pipe averaged 3.1 × 10(3) and 1.9 × 10(4) CFU cm(-2), respectively. The study shows that production of MIB is associated with changes in chlorine residual in the systems. This is the first report of cyclic chlorine shock as a stimulus for MIB production by actinomycetes in drinking water distribution system's ecology.

  7. Improved method generates more chlorine dioxide

    SciTech Connect

    Jordan, R.W.; Kosinski, A.J.; Baker, R.J.

    1980-10-01

    The addition of acid can greatly improve the chlorine-chlorite process and enhance the use of chlorine dioxide as an alternative to chlorine for disinfection. The process is economical for use in taste and odor control, and for manganese, oxidation. The maximum yield is obtained using no excess chlorine, and the amount of unreacted sodium chlorite and chlorine in the product stream is reduced. (1 diagram, 4 graphs, 9 references)

  8. CHLORINE INACTIVATION OF BACILLUS ENDOSPORES

    EPA Science Inventory

    The possibility of a bioterrorism event resulting in the release of Bacillus anthracis endospores into a drinking water distribution system necessitates research into means by which these endospores can be inactivated. This study was designed to determine the chlorine resistance...

  9. Chlorine Isotope Variation in Eucrites

    NASA Astrophysics Data System (ADS)

    Barrett, T. J.; Barnes, J. J.; Anand, M.; Franchi, I. A.; Greenwood, R. C.; Charlier, B. L. A.; Grady, M. M.

    2016-08-01

    We present Cl isotopic compositions for several eucrites with a wide range of petrological and geochemical histories. Our results include some of the heaviest chlorine isotopic compositions recorded so far in the solar system.

  10. Microbial degradation of chlorinated acetophenones

    SciTech Connect

    Havel, J.; Reineke, W. )

    1993-08-01

    Chlorinated acetophenones can originate from several sources: insecticides and as by-products of degradation of chlorosubstituted xanthones, PCPs, ethylbenzene, and styrene. This paper describes the isolation and characterization of a mixed culture which mineralizes 4-chloroacetophenone. Arthrobacter sp., found in the mixed culture, was found to utilize 4-chloroacetophenone for growth and was able to mineralize a broad spectrum of chlorinated acetophenones. 29 refs., 6 figs. 2 tabs.

  11. Chlorination of Pyridinium Compounds

    PubMed Central

    Daumer, Kathleen M.; Khan, Ahsan U.; Steinbeck, Marla J.

    2010-01-01

    Reactive oxygen species produced by activated neutrophils and monocytes are thought to be involved in mediating the loss of collagen and other matrix proteins at sites of inflammation. To evaluate their potential to oxidize the pyridinoline (Pyd) cross-links found in collagen types I and II, we reacted hydrogen peroxide (H2O2), hypochlorous acid/hypochlorite (HOCl/OCl−), and singlet oxygen (O2(1Δg)) with the Pyd substitutes, pyridoxamine dihydrochloride and vitamin B6, which share the same chemical structure and spectral properties of Pyd cross-links. Neither H2O2 (125–500 µm) nor O2(1Δg) (10–25 µm) significantly changed the spectral properties of pyridoxamine or vitamin B6. Reaction of HOCl/OCl− (12.5–50 µm) with pyridoxamine at pH 7.2 resulted in a concentration-dependent appearance of two new absorbance peaks and a decrease in fluorescence at 400 nm (excitation 325 nm). The new absorbance peaks correlated with the formation of an N-chloramine and the product of its subsequent reaction with pyridoxamine. In contrast, the extent to which HOCl reacted with vitamin B6, which lacks a primary amine group, was variable at this pH. At lysosomal pH 5.5, Cl2/HOCl/OCl− reacted with both pyridoxamine and vitamin B6. Four of the chlorinated products of this reaction were identified by gas chromatography-mass spectrometry and included 3-chloropyridinium, an aldehyde, and several chlorinated products with disrupted rings. To evaluate the effects of Cl2/HOCl/OCl− on Pyd cross-links in collagen, we exposed bone collagen type I and articular cartilage type II to HOCl. Treatment of either collagen type with HOCl at pH 5.0 or 7.2 resulted in the oxidation of amine groups and, for collagen type II, the specific decrease in Pyd cross-link fluorescence, suggesting that during inflammation both oxidations may be used by neutrophils and monocytes to promote the loss of matrix integrity. PMID:10940296

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

    NASA Astrophysics Data System (ADS)

    Hsu, Leo H. H.; Hoque, Enamul; Kruse, Peter; Ravi Selvaganapathy, P.

    2015-02-01

    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.

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

    SciTech Connect

    Hsu, Leo H. H.; Hoque, Enamul; Kruse, Peter; Ravi Selvaganapathy, P.

    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.

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

    PubMed

    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%.

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

    PubMed

    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%. PMID:24534637

  16. Transformation of iopamidol during chlorination.

    PubMed

    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. In situ bioremediation of chlorinated solvents

    SciTech Connect

    Sack, W.A.; Carriere, P.E.; Whiteman, C.S.; Davis, M.P.; Raman, S.; Cuddeback, J.E.; Shiemke, A.K.

    1995-12-31

    In situ bioremediation of chlorinated organic is receiving growing support and widespread testing in the field. It is an attractive alternative with the potential to destroy contaminants almost completely. The research seeks to exploit the natural symbiotic relationship between methanogenic and methanotrophic microorganisms. The methanogens are able to carry out anaerobic reductive dehalogenation of highly chlorinated solvents while producing methane. The methanotrophs in turn utilize the end products of the methanogens, including the methane, to aerobically degrade the residual CAH compounds to environmentally acceptable end products. Both groups of organisms degrade the CAH compounds cometabolically and require a primary substrate. The purpose of the research is to evaluate and optimize the ability of methanotrophic, methanogenic, and other selected bacteria for cost-effective biotransformation of TCE and other volatile organic compounds (VOCs). This paper describes initial studies using separate anaerobic and aerobic columns. As soon as the initial column studies are complete, the anaerobic and aerobic columns will be combined in both sequential and simultaneous modes to evaluate complete CAH destruction.

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

    EPA Science Inventory

    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. IDENTIFICATION OF NEW DRINKING WATER DISINFECTION BY-PRODUCTS FROM OZONE, CHLORINE DIOXIDE, CHLORAMINE, AND CHLORINE

    EPA Science Inventory

    Due to concern over the potential adverse health effects of trihalomethanes (THMs) and other chlorinated by-products in chlorinated drinking water, alternative disinfection methods are being explored. Ozone, chlorine dioxide, and chloramine are currently popular alternatives to ...

  20. Cleaning without chlorinated solvents

    SciTech Connect

    Thompson, L.M.; Simandl, R.F.

    1994-12-31

    Because of health and environmental concerns, many regulations have been passed in recent years regarding the use of chlorinated solvents. The Oak Ridge Y-12 Plant has had an active program to find alternatives for these solvents used in cleaning applications for the past 7 years. During this time frame, the quantity of solvents purchased has been reduced by 92%. The program has been a twofold effort. Vapor degreasers used in batch cleaning-operations have been replaced by ultrasonic cleaning with aqueous detergent, and other organic solvents have been identified for use in hand-wiping or specialty operations. In order to qualify these alternatives for use, experimentation was conducted on cleaning ability as well as effects on subsequent operations such as welding, painting and bonding. Cleaning ability was determined using techniques such as X-ray photoelectron spectroscopy (XPS) and Fourier Transform Infrared Spectroscopy (FTIR) which are capable of examining monolayer levels of contamination on a surface. Solvents have been identified for removal of rust preventative oils, lapping oils, machining coolants, lubricants, greases, and mold releases. Solvents have also been evaluated for cleaning urethane foam spray guns, swelling of urethanes and swelling of epoxies.

  1. Cleaning without chlorinated solvents

    NASA Technical Reports Server (NTRS)

    Thompson, L. M.; Simandl, R. F.

    1995-01-01

    Because of health and environmental concerns, many regulations have been passed in recent years regarding the use of chlorinated solvents. The Oak Ridge Y-12 Plant has had an active program to find alternatives for these solvents used in cleaning applications for the past 7 years. During this time frame, the quantity of solvents purchased has been reduced by 92 percent. The program has been a twofold effort. Vapor degreasers used in batch cleaning operations have been replaced by ultrasonic cleaning with aqueous detergent, and other organic solvents have been identified for use in hand-wiping or specialty operations. In order to qualify these alternatives for use, experimentation was conducted on cleaning ability as well as effects on subsequent operations such as welding, painting, and bonding. Cleaning ability was determined using techniques such as x-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR) which are capable of examining monolayer levels of contamination on a surface. Solvents have been identified for removal of rust preventative oils, lapping oils, machining coolants, lubricants, greases, and mold releases. Solvents have also been evaluated for cleaning urethane foam spray guns, swelling of urethanes, and swelling of epoxies.

  2. Organo-Chlorinated Thin Films Deposited by Atmospheric Pressure Plasma-Enhanced Chemical Vapor Deposition for Adhesion Enhancement between Rubber and Zinc-Plated Steel Monofilaments.

    PubMed

    Vandenabeele, Cédric; Bulou, Simon; Maurau, Rémy; Siffer, Frederic; Belmonte, Thierry; Choquet, Patrick

    2015-07-01

    A continuous-flow plasma process working at atmospheric pressure is developed to enhance the adhesion between a rubber compound and a zinc-plated steel monofilament, with the long-term objective to find a potential alternative to the electrolytic brass plating process, which is currently used in tire industry. For this purpose, a highly efficient tubular dielectric barrier discharge reactor is built to allow the continuous treatment of "endless" cylindrical substrates. The best treatment conditions found regarding adhesion are Ar/O2 plasma pretreatment, followed by the deposition from dichloromethane of a 75 nm-thick organo-chlorinated plasma polymerized thin film. Ar/O2 pretreatment allows the removal of organic residues, coming from drawing lubricants, and induces external growth of zinc oxide. The plasma layer has to be preferably deposited at low power to conserve sufficient hydrocarbon moieties. Surface analyses reveal the complex chemical mechanism behind the establishment of strong adhesion levels, more than five times higher after the plasma treatment. During the vulcanization step, superficial ZnO reacts with the chlorinated species of the thin film and is converted into porous and granular bump-shaped ZnwOxHyClz nanostructures. Together, rubber additives diffuse through the plasma layer and lead to the formation of zinc sulfide on the substrate surface. Hence, two distinct interfaces, rubber/thin film and thin film/substrate, are established. On the basis of these observations, hypotheses explaining the high bonding strength results are formulated. PMID:26069994

  3. Organo-Chlorinated Thin Films Deposited by Atmospheric Pressure Plasma-Enhanced Chemical Vapor Deposition for Adhesion Enhancement between Rubber and Zinc-Plated Steel Monofilaments.

    PubMed

    Vandenabeele, Cédric; Bulou, Simon; Maurau, Rémy; Siffer, Frederic; Belmonte, Thierry; Choquet, Patrick

    2015-07-01

    A continuous-flow plasma process working at atmospheric pressure is developed to enhance the adhesion between a rubber compound and a zinc-plated steel monofilament, with the long-term objective to find a potential alternative to the electrolytic brass plating process, which is currently used in tire industry. For this purpose, a highly efficient tubular dielectric barrier discharge reactor is built to allow the continuous treatment of "endless" cylindrical substrates. The best treatment conditions found regarding adhesion are Ar/O2 plasma pretreatment, followed by the deposition from dichloromethane of a 75 nm-thick organo-chlorinated plasma polymerized thin film. Ar/O2 pretreatment allows the removal of organic residues, coming from drawing lubricants, and induces external growth of zinc oxide. The plasma layer has to be preferably deposited at low power to conserve sufficient hydrocarbon moieties. Surface analyses reveal the complex chemical mechanism behind the establishment of strong adhesion levels, more than five times higher after the plasma treatment. During the vulcanization step, superficial ZnO reacts with the chlorinated species of the thin film and is converted into porous and granular bump-shaped ZnwOxHyClz nanostructures. Together, rubber additives diffuse through the plasma layer and lead to the formation of zinc sulfide on the substrate surface. Hence, two distinct interfaces, rubber/thin film and thin film/substrate, are established. On the basis of these observations, hypotheses explaining the high bonding strength results are formulated.

  4. Hydrocarbon residues in tissues of sea otters (`enhydra lutris`) collected following the Exxon Valdez oil spill. Marine mammal study 6-16. Exxon Valdez oil spill state/federal natural resource damage assessment. Final report

    SciTech Connect

    Ballachey, B.E.; Kloecker, K.A.

    1997-04-01

    Ten moderately to heavily oiled sea otters were collected in Prince William Sound during the Exxon Valdez oil spill and up to seven tissues from each were analyzed for hydrocarbons. Aliphatic and aromatic hydrocarbons were detected in all tissues. Concentrations of aromatic hydrocarbons in fat samples were an order of magnitude higher than in other tissues. The patterns of distribution of these hydrocarbons suggested crude oil as the source of contamination. However, there was variation among oiled otters in the concentrations of individual hydrocarbons, which may be due to differing proximate causes of mortality and varying lengths of time and sea otters survived following oil exposure. The concentrations of both aliphatic and aromatic hydrocarbons in the tissues of the ten oiled sea otters generally were higher than in tissues from 7 sea otters with no external oiling that were collected from prince William Sound in 1989 and 1990, or from 12 sea otters collected from an area in southeast Alaska which had not experienced an oil spill.

  5. Kinetics of reactions between chlorine and the cyanobacterial toxins microcystins.

    PubMed

    Acero, Juan L; Rodriguez, Eva; Meriluoto, Jussi

    2005-04-01

    Blooms of cyanobacteria can give rise to the production of toxins which contaminate drinking water sources. Among the oxidants and disinfectants typically applied in waterworks, chlorine has been found to be effective for the degradation of microcystins. In the present study, unknown second-order rate constants for the reactions of microcystin-LR (MC-LR), -RR and -YR with chlorine were determined over a wide pH range. It was found that an increase of pH has a negative effect on the microcystin degradation rate. Apparent second-order rate constant for the chlorination of MC-LR at 20 degrees C varied from 475 M(-1)s(-1) at pH 4.8 to 9.8 M(-1)s(-1) at pH 8.8. From these apparent second-order rate constants, rate constants for the reactions of MC-LR with hypochlorous acid (HOCl) and hypochlorite (ClO-) were evaluated. Half-life times ranged from minutes at pH 6 to 1 h at pH 8 for a constant residual chlorine concentration of 1.0-0.5 mgl(-1), typical of oxidation pre-treatment and final disinfection. Similar reactivity with chlorine was found for MC-RR and MC-YR. Therefore, chlorination is a feasible option for microcystin degradation during oxidation and disinfection processes, and can be applied in drinking water treatment in case of cyanobacterial toxin risk if the pH is kept below 8.

  6. Application of Chlorine-Assisted Chemical Vapor Deposition of Diamond at Low Temperatures

    NASA Technical Reports Server (NTRS)

    Pan, Chenyu; Altemir, David A.; Margrave, John L.; Hauge, Robert H.

    1994-01-01

    Low temperature deposition of diamond has been achieved by a chlorine-assisted diamond chemical vapor deposition (CA-CVD) process. This method begins with the thermal dissociation of molecular chlorine into atomic chlorine in a resistively heated graphite furnace at temperatures between 1300 and 1500 deg. C. The atomic chlorine, upon mixing, subsequently reacts with molecular hydrogen and hydrocarbons. The rapid exchange reactions between the atomic chlorine, molecular hydrogen, and hydrocarbons give rise to the atomic hydrogen and carbon precursors required for diamond deposition. Homoepitaxial diamond growth on diamond substrates has been studied over the substrate temperature range of 100-950 C. It was found that the diamond growth rates are approximately 0.2 microns/hr in the temperature range between 102 and 300 C and that the growth rates do not decrease significantly with a decrease in substrate temperature. This is unique because the traditional diamond deposition using H2/CH4 systems usually disappears at substrate temperatures below approx. 500 deg. C. This opens up a possible route to the deposition of diamond on low-melting point materials such as aluminum and its alloys.

  7. Persistence of pharmaceuticals and other organic compounds in chlorinated drinking water as a function of time

    USGS Publications Warehouse

    Gibs, J.; Stackelberg, P.E.; Furlong, E.T.; Meyer, M.; Zaugg, S.D.; Lippincott, R.L.

    2007-01-01

    Ninety eight pharmaceuticals and other organic compounds (POOCs) that were amended to samples of chlorinated drinking-water were extracted and analyzed 1, 3, 6, 8, and 10 days after amendment to determine whether the total chlorine residual reacted with the amended POOCs in drinking water in a time frame similar to the residence time of drinking water in a water distribution system. Results indicated that if all 98 were present in the finished drinking water from a drinking-water treatment plant using free chlorine at 1.2??mg/L as the distribution system disinfectant residual, 52 POOCs would be present in the drinking water after 10??days at approximately the same concentration as in the newly finished drinking water. Concentrations of 16 POOCs would be reduced by 32% to 92%, and 22 POOCs would react completely with residual chlorine within 24??h. Thus, the presence of free chlorine residual is an effective means for transforming some POOCs during distribution. ?? 2006 Elsevier B.V. All rights reserved.

  8. Evaluation of the use of chlorine dioxide to control zebra mussels

    SciTech Connect

    Tsou, J.; Coyle, J.; Pallo, S.

    1995-06-01

    Chlorine dioxide was tested as a zebra mussel biocide at two steam electric generating stations in Illinois. The purpose of these studies was to determine the efficacy of chlorine dioxide in killing zebra mussels and to develop site specific treatment programs for the two utilities. The Electric Power Research Institute (EPRI) Zebra Mussel Consortium sponsored the testing of this recent use of chlorine dioxide. The raw water system at Central Illinois Public Service`s Meredosia Station, on the Illinois River, received two to four day applications of chlorine dioxide in April, July, and September 1994. The raw water system at Illinois Power Company`s Wood River Station, on the Mississippi River, received two to four day applications in July 1993, January, April, May, July, and September 1994. Chlorine dioxide was generated on-site and injected into the water intake structure, in front of or just behind the traveling screens, at both power stations. Both cooling and service water systems were treated at the facilities. Various water quality parameters, including residual chlorine in the discharge effluent, were measured during the studies. Residual chlorine was neutralized with sodium bisulfite prior to discharge at both plants. Bioboxes, containing healthy zebra mussels, were placed at various strategic locations throughout the power stations. Control bioboxes were also placed in the rivers, upstream of the chlorine dioxide injection locations. Results of the chlorine dioxide applications varied from 35 percent to 100 percent. These varied results appear to be related to seasonal water temperature differences, water quality, and/or plant design. Mortality differences were also noted in bioboxes which contained zebra mussels imported from Lake Erie and those which contained local mussels. These and other data are presented.

  9. Debate over phaseout of chlorine, chlorinated organics continues

    SciTech Connect

    Hileman, B. )

    1993-12-06

    During the past two months, the debate over whether to phase out the use and production of chlorine and chlorinated organics as a broad class of chemicals has continued on a number of fronts. This question was the major focus of discussion at the recent biennial meeting in Windsor Ontario, of the International Joint Commission (IJC)--a binational group that oversees implementation of the Great Lakes Water Quality Agreement. Just prior to the meeting, the governments of the US and Canada presented their views on this issue, and it was the topic most of the speakers discussed during the organized sessions and public hearings. IJC is working on its seventh Biennial Report, which will be completed shortly after the first of the year. The very large comprehensive study on the health and environmental effects of chlorinated organics being prepared by CanTox, a consulting group in Mississauga, Ontario, for CCC and the Chlorine Institute was originally scheduled to be published in June. It is now slated for release sometime in early 1994, and the conference on the health and environmental effects of chlorinated organics that was to be sponsored by CCC and held in September of this year was canceled and has not been rescheduled. The movement to phase out chlorine also may be gathering momentum in Europe. On Oct 15, the 21 nations party to the Barcelona Convention on pollution of the Mediterranean recommended that their governments phase out toxic, persistent, and bioaccumulative substances, especially organohalogens (which include organochlorine), by 2005. This action is similar to proposals made in September 1992 by the Paris Commission, which oversees discharges of pollutants in the northeast Atlantic Ocean.

  10. Biological Instability in a Chlorinated Drinking Water Distribution Network

    PubMed Central

    Nescerecka, Alina; Rubulis, Janis; Vital, Marius; Juhna, Talis; Hammes, Frederik

    2014-01-01

    The purpose of a drinking water distribution system is to deliver drinking water to the consumer, preferably with the same quality as when it left the treatment plant. In this context, the maintenance of good microbiological quality is often referred to as biological stability, and the addition of sufficient chlorine residuals is regarded as one way to achieve this. The full-scale drinking water distribution system of Riga (Latvia) was investigated with respect to biological stability in chlorinated drinking water. Flow cytometric (FCM) intact cell concentrations, intracellular adenosine tri-phosphate (ATP), heterotrophic plate counts and residual chlorine measurements were performed to evaluate the drinking water quality and stability at 49 sampling points throughout the distribution network. Cell viability methods were compared and the importance of extracellular ATP measurements was examined as well. FCM intact cell concentrations varied from 5×103 cells mL−1 to 4.66×105 cells mL−1 in the network. While this parameter did not exceed 2.1×104 cells mL−1 in the effluent from any water treatment plant, 50% of all the network samples contained more than 1.06×105 cells mL−1. This indisputably demonstrates biological instability in this particular drinking water distribution system, which was ascribed to a loss of disinfectant residuals and concomitant bacterial growth. The study highlights the potential of using cultivation-independent methods for the assessment of chlorinated water samples. In addition, it underlines the complexity of full-scale drinking water distribution systems, and the resulting challenges to establish the causes of biological instability. PMID:24796923

  11. Biological instability in a chlorinated drinking water distribution network.

    PubMed

    Nescerecka, Alina; Rubulis, Janis; Vital, Marius; Juhna, Talis; Hammes, Frederik

    2014-01-01

    The purpose of a drinking water distribution system is to deliver drinking water to the consumer, preferably with the same quality as when it left the treatment plant. In this context, the maintenance of good microbiological quality is often referred to as biological stability, and the addition of sufficient chlorine residuals is regarded as one way to achieve this. The full-scale drinking water distribution system of Riga (Latvia) was investigated with respect to biological stability in chlorinated drinking water. Flow cytometric (FCM) intact cell concentrations, intracellular adenosine tri-phosphate (ATP), heterotrophic plate counts and residual chlorine measurements were performed to evaluate the drinking water quality and stability at 49 sampling points throughout the distribution network. Cell viability methods were compared and the importance of extracellular ATP measurements was examined as well. FCM intact cell concentrations varied from 5×10(3) cells mL(-1) to 4.66×10(5) cells mL(-1) in the network. While this parameter did not exceed 2.1×10(4) cells mL(-1) in the effluent from any water treatment plant, 50% of all the network samples contained more than 1.06×10(5) cells mL(-1). This indisputably demonstrates biological instability in this particular drinking water distribution system, which was ascribed to a loss of disinfectant residuals and concomitant bacterial growth. The study highlights the potential of using cultivation-independent methods for the assessment of chlorinated water samples. In addition, it underlines the complexity of full-scale drinking water distribution systems, and the resulting challenges to establish the causes of biological instability.

  12. Zebra mussel control using periodic chlorine dioxide treatments. Final report

    SciTech Connect

    Mussalli, Y.G.; Martin, P.D.

    1995-11-01

    Chlorine dioxide was injected into the water intakes at two power plants in Illinois and one in Indiana in an effort to eradicate the existing population of zebra mussels and mitigate further settlement in station river water cooling systems. Results of the treatments at Illinois Power Company`s Wood River Station on the Mississippi River, Central Illinois Public Service`s Meredosia Station on the Illinois River, and SI Energy`s Gallagher Station on the Ohio River are reported. Treatments were performed on a turnkey basis, with three treatments performed at Meredosia Station in 1994, six treatments performed at Wood River Station between July 1993 and September 1994, and 2 treatments performed at Gallagher Station in 1994. For each treatment, a contractor installed and operated a portable chlorine dioxide generator, monitored water quality and oxidant levels, and provided and monitored bioboxes containing test mussels. Results of the treatments were very favorable, indicating a good potential for periodic treatments with chlorine dioxide to control zebra mussel infestations in the raw water systems of power plants and other industrial facilities. Some difficulties with the chlorine dioxide generation system and cold temperature effects reduced the treatment effectiveness, particularly the second treatment at Gallagher Station. Average induced mortalities ranged from 70 to 100% at Wood River, 87 to 92% at Meredosia, and 30 to 100% at Gallagher for native mussels. Dechlorination successfully kept total oxidant residual levels at or below 0.05 ppM during all treatments at all stations.

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

    PubMed

    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.

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

    PubMed

    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

  15. Detection of chlorinated aromatic compounds

    DOEpatents

    Ekechukwu, A.A.

    1996-02-06

    A method for making a composition for measuring the concentration of chlorinated aromatic compounds in aqueous fluids, and an optical probe for use with the method are disclosed. The composition comprises a hydrophobic polymer matrix, preferably polyamide, with a fluorescent indicator uniformly dispersed therein. The indicator fluoresces in the presence of the chlorinated aromatic compounds with an intensity dependent on the concentration of these compounds in the fluid of interest, such as 8-amino-2-naphthalene sulfonate. The probe includes a hollow cylindrical housing that contains the composition in its distal end. The probe admits an aqueous fluid to the probe interior for exposure to the composition. An optical fiber transmits excitation light from a remote source to the composition while the indicator reacts with chlorinated aromatic compounds present in the fluid. The resulting fluorescence light signal is reflected to a second optical fiber that transmits the light to a spectrophotometer for analysis. 5 figs.

  16. Stable Chlorine Isotope Fractionation

    NASA Astrophysics Data System (ADS)

    Sharp, Z.

    2006-12-01

    Chlorine isotope partitioning between different phases is not well understood. Pore fluids can have δ37Cl values as low as -8‰, with neoform sediments having strongly positive values. Most strikingly, volcanic gases have δ37Cl values that cover a range in excess of 14‰ (Barnes et al., this meeting). The large range is difficult to explain in terms of equilibrium fractionation, which, although calculated to be very large for Cl in different oxidation states, should be less than 2‰ between chloride species (Schauble et al., 2003, GCA). To address the discrepancy between Nature and theory, we have measured Cl isotope fractionation for selected equilibrium and disequilibrium experiments in order to identify mechanisms that might lead to large fractionations. 1) NaCl (s,l) NaCl (v): NaCl was sealed in an evacuated silica tube and heated at one end, causing vaporization and reprecipitation of NaCl (v) at the cool end of the tube. The fractionation is 0.2‰ at 700°C (halite-vapor) and 0.7‰ at 800°C (liquid-vapor), respectively. The larger fractionation at higher temperature may be related to equilibrium fractionation between liquid and gas vs. `stripping' of the solid in the lower T experiments. 2) Sodalite NaCl(l): Nepheline and excess NaCl were sealed in a Pt crucible at 825°C for 48 hrs producing sodalite. The measured newly-formed sodalite-NaCl fractionation is -0.2‰. 3) Volatilization of HCl: Dry inert gas was bubbled through HCl solutions and the vapor was collected in a downstream water trap. There was no fractionation for 12.4M HCl (HCl fuming) vapor at 25°C. For a 1 M boiling HCl solution, the HCl-vapor fractionation was ~9‰. The difference is probably related to the degree of dissociation in the acid, with HCl dissolved in water for the highly acidic solutions, and dissociated H3O+ and Cl- for lower concentrations. The HCl volatilization experiments are in contrast to earlier vapor-liquid experiments in NaCl-H2O system, where fractionation was

  17. SPME-GC-EC of chlorinated paraffins in water

    SciTech Connect

    Webster, G.R.B.; Sarna, L.P.; Thomas, D.A.

    1995-12-31

    Contamination of aquatic ecosystems with chlorinated organic contaminants is an increasing toxicological problem. Chlorinated paraffins (CPs) are a class of compounds which are used as fire retardants in paints and as high pressure lubricants and are classified as Priority Toxic Substances under the Canadian Environmental Protection Act (CEPA). As the largest group of high molecular weight chlorinated hydrocarbons produced in Western Europe and North America, CPs have recently come under increased regulatory scrutiny in Canada, the USA, and Europe, because of concerns about their environmental persistence, possible adverse effects on terrestrial and aquatic organisms, and potential carcinogenicity to humans. In both the monitoring of such contamination and the determination of the success of remediation methods, straightforward and inexpensive analytical methodology increases the ease of environmental assessment and facilitates regulatory enforcement. CPs have been considered to be incapable of being analyzed by GC. The authors report the solid phase microextraction (SPME) based analysis of CPs by GC using electron capture (EC) detection. Both synthetic C{sub 10} standards and fractionated commercially derived material have been analyzed by this method in water.

  18. PPCP degradation by UV/chlorine treatment and its impact on DBP formation potential in real waters.

    PubMed

    Yang, Xin; Sun, Jianliang; Fu, Wenjie; Shang, Chii; Li, Yin; Chen, Yiwei; Gan, Wenhui; Fang, Jingyun

    2016-07-01

    The ultraviolet/chlorine (UV/chlorine) water purification process was evaluated for its ability to degrade the residues of pharmaceuticals and personal care products (PPCPs) commonly found in drinking water sources. The disinfection byproducts (DBPs) formed after post-chlorination were documented. The performance of the UV/chlorine process was compared with that of the UV/hydrogen peroxide (UV/H2O2) process in treating three types of sand-filtered natural water. Except caffeine and carbamazepine residues, the UV/chlorine process was found to be 59-99% effective for feed water with a high level of dissolved organic carbon and alkalinity, and 27-92% effective for water with a high ammonia content. Both chlorine radicals and hydroxyl radicals were found to contribute to the observed PPCP degradation. The removal efficiencies of chlorine- and UV-resistant PPCPs such as carbamazepine and caffeine were 2-3 times greater than in the UV/H2O2 process in waters not enriched with ammonia. UV/chlorine treatment slightly enhanced the formation chloral hydrate (CH), haloketone (HK) and trichloronitromethane (TCNM). It reduced haloacetonitrile (HAN) formation during the post-chlorination in comparison with the UV/H2O2 process. In waters with high concentrations of ammonia, the UV/chlorine process was only 5-7% more effective than the UV/H2O2 process, and it formed slightly more THMs, HKs and TCNM along with reduced formation of CH and HAN. The UV/chlorine process is thus recommended as a good alternative to UV/H2O2 treatment for its superior PPCP removal without significantly enhancing DBP formation.

  19. PPCP degradation by UV/chlorine treatment and its impact on DBP formation potential in real waters.

    PubMed

    Yang, Xin; Sun, Jianliang; Fu, Wenjie; Shang, Chii; Li, Yin; Chen, Yiwei; Gan, Wenhui; Fang, Jingyun

    2016-07-01

    The ultraviolet/chlorine (UV/chlorine) water purification process was evaluated for its ability to degrade the residues of pharmaceuticals and personal care products (PPCPs) commonly found in drinking water sources. The disinfection byproducts (DBPs) formed after post-chlorination were documented. The performance of the UV/chlorine process was compared with that of the UV/hydrogen peroxide (UV/H2O2) process in treating three types of sand-filtered natural water. Except caffeine and carbamazepine residues, the UV/chlorine process was found to be 59-99% effective for feed water with a high level of dissolved organic carbon and alkalinity, and 27-92% effective for water with a high ammonia content. Both chlorine radicals and hydroxyl radicals were found to contribute to the observed PPCP degradation. The removal efficiencies of chlorine- and UV-resistant PPCPs such as carbamazepine and caffeine were 2-3 times greater than in the UV/H2O2 process in waters not enriched with ammonia. UV/chlorine treatment slightly enhanced the formation chloral hydrate (CH), haloketone (HK) and trichloronitromethane (TCNM). It reduced haloacetonitrile (HAN) formation during the post-chlorination in comparison with the UV/H2O2 process. In waters with high concentrations of ammonia, the UV/chlorine process was only 5-7% more effective than the UV/H2O2 process, and it formed slightly more THMs, HKs and TCNM along with reduced formation of CH and HAN. The UV/chlorine process is thus recommended as a good alternative to UV/H2O2 treatment for its superior PPCP removal without significantly enhancing DBP formation. PMID:27110887

  20. Field-usable portable analyzer for chlorinated organic compounds

    SciTech Connect

    Buttner, W.J.; Penrose, W.R.; Stetter, J.R.

    1995-10-01

    Transducer Research, Inc. (TRI) has been working with the DOE Morgantown Energy Technology Center to develop a new chemical monitor based on a unique sensor which responds selectively to vapors of chlorinated solvents. We are also developing field applications for the monitor in actual DOE cleanup operations. During the initial phase, prototype instruments were built and field tested. Because of the high degree of selectivity that is obtained, no response was observed with common hydrocarbon organic compounds such as BTX (benzene, toluene, xylene) or POLs (petroleum, oil, lubricants), and in fact, no non-halogen-containing chemical has been identified which induces a measurable response. By the end of the Phase I effort, a finished instrument system was developed and test marketed. This instrument, called the RCL MONITOR, was designed to analyze individual samples or monitor an area with automated repetitive analyses. Vapor levels between 0 and 500 ppm can be determined in 90 s with a lower detection limit of 0.2 ppm using the handportable instrument. In addition to the development of the RCL MONITOR, advanced sampler systems are being developed to: (1) extend the dynamic range of the instrument through autodilution of the vapor and (2) allow chemical analyses to be performed on aqueous samples. When interfaced to the samplers, the RCL MONITOR is capable of measuring chlorinated solvent contamination in the vapor phase up to 5000 ppm and in water and other condensed media from 10 to over 10,000 ppb(wt)--without hydrocarbon and other organic interferences.

  1. 21 CFR 177.1610 - Polyethylene, chlorinated.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... chlorine, as determined by ASTM 1method D1303-55 (Reapproved 1979), “Standard Test Method for Total Chlorine in Vinyl Chloride Polymers and Copolymers,” which is incorporated by reference (Copies may...

  2. 40 CFR 704.43 - Chlorinated naphthalenes.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... weight of chlorine. (2) Import means to import in bulk form or as part of a mixture. (3) Isomeric ratio... the chlorine atom(s) on the naphthalene. (4) Polychlorinated biphenyl means any chemical...

  3. 21 CFR 177.1610 - Polyethylene, chlorinated.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... chlorine, as determined by ASTM 1method D1303-55 (Reapproved 1979), “Standard Test Method for Total Chlorine in Vinyl Chloride Polymers and Copolymers,” which is incorporated by reference (Copies may...

  4. THE ROLE OF CHLORINE IN DIOXIN FORMATION

    EPA Science Inventory

    There is poor correlation between total chlorine in waste streams and formation of polychlorinated dibenzodioxin and polychlorinated dibenzofuran (PCDD/F) during waste combustion. This is because the active chlorine (Cl) species are strongly dependent upon combustion conditions. ...

  5. Colorectal cancers and chlorinated water

    PubMed Central

    El-Tawil, Ahmed Mahmoud

    2016-01-01

    Published reports have revealed increased risk of colorectal cancers in people exposed to chlorinated drinking water or chemical derivatives of chlorination. Oestrogen plays a dual positive functions for diminishing the possibilities of such risk by reducing the entrance, and increasing the excretion, of these chemicals. In addition, there are supplementary measures that could be employed in order to reduce this risk further, such as boiling the drinking water, revising the standard concentrations of calcium, magnesium and iron in the public drinking water and prescribing oestrogen in susceptible individuals. Hypo-methylation of genomic DNA could be used as a biological marker for screening for the potential development of colorectal cancers. PMID:27096035

  6. STABLE CHLORINE ISOTOPE ANALYSIS OF CHLORINATED ORGANIC CONTAMINANTS

    EPA Science Inventory

    The biogeochemical cycling of chlorinated organic contaminants in the environment is often difficult to understand because of the complex distributions of these compounds and variability of sources. To address these issues from an isotopic perspective, we have measured the, 37Cl...

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

    SciTech Connect

    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.

  8. Effect of turbidity on chlorination efficiency and bacterial persistence in drinking water.

    PubMed

    LeChevallier, M W; Evans, T M; Seidler, R J

    1981-07-01

    To define interrelationships between elevated turbidities and the efficiency of chlorination in drinking water, experiments were performed to measure bacterial survival, chlorine demand, and interference with microbiological determinations. Experiments were conducted on the surface water supplies for communities which practice chlorination as the only treatment. Therefore, the conclusions of this study apply only to such systems. Results indicated that disinfection efficiency (log10 of the decrease in coliform numbers) was negatively correlated with turbidity and was influenced by season, chlorine demand of the samples, and the initial coliform level. Total organic carbon was found to be associated with turbidity and was shown to interfere with maintenance of a free chlorine residual by creating a chlorine demand. Interference with coliform detection in turbid waters could be demonstrated by the recovery of typical coliforms from apparently negative filters. The incidence of coliform masking in the membrane filter technique was found to increase as the turbidity of the chlorinated samples increased. the magnitude of coliform masking in the membrane filter technique increased from less than 1 coliform per 100 ml in water samples of less than 5 nephelometric turbidity units to greater than 1 coliform per 100 ml in water samples of greater than 5 nephelometric turbidity units. Statistical models were developed to predict the impact of turbidity on drinking water quality. The results justify maximum contaminant levels for turbidity in water entering a distribution system as stated in the National Primary Drinking Water Regulations of the Safe Drinking Water Act. PMID:7259162

  9. Environmental distribution of chlorinated organic pollutants

    SciTech Connect

    Emmi, F.

    1983-01-01

    A survey of the concentration of PCB's and chlorinated hydrocarbon pesticides in Susquehanna River Basin sediments was performed on samples collected from New York and Pennsylvania in 1976-1979. Highest concentrations were found for PCB's, with median and range of 38 and 13-524 ng/g, respectively. Pesticides had median concentrations ranging from approx.1 ng/g for DDT, DDD, and DDE, to less than 0.1 ng/g for aldrin and dieldrin. Highest concentrations generally were found downstream from industrial centers. Concentrations of PCB's and pesticides were also determined for soil composites collected from six areas of the basin. For several pollutants, the highest levels were found in the Pennsylvania areas, especially the Conestoga River Basin site. The PCB levels were the same (approx.35 ng/g) in all New York soil composites; this was consistent with concentrations predicted from known atmospheric deposition data. Adsorption of atrazine and simazine on model substrates was stuided to elucidate the partitioning of these herbicides on river sediments. Clean sea sand had little affinity for these compounds. Adsorption on illite clay and humic acid-coated sea sand gave relatively large K/sub p/ and K/sub oc/ values compared to the values for river sediments, suggesting that the nature of the sites available for absorbing organic molecules needs further study.

  10. Effect of moisture, charge size, and chlorine concentration on PCDD/F emissions from simulated open burning of forest biomass

    EPA Science Inventory

    Loblolly pine (Pinus taeda) was combusted at different charge sizes, fuel moisture, and chlorine content to determine the effect on emissions of polychlorinated dibenzo-p-dioxins and polychlorinated diberizofurans (PCDDslFs) as well as co-pollutants CO, PM, and total hydrocarbons...

  11. 49 CFR 179.102-2 - Chlorine.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 49 Transportation 3 2012-10-01 2012-10-01 false Chlorine. 179.102-2 Section 179.102-2... Tank Car Tanks (Classes DOT-105, 109, 112, 114 and 120) § 179.102-2 Chlorine. (a) Each tank car used to transport chlorine must comply with all of the following: (1) Tanks must be fabricated from carbon...

  12. 49 CFR 179.102-2 - Chlorine.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 49 Transportation 3 2011-10-01 2011-10-01 false Chlorine. 179.102-2 Section 179.102-2... Tank Car Tanks (Classes DOT-105, 109, 112, 114 and 120) § 179.102-2 Chlorine. (a) Each tank car used to transport chlorine must comply with all of the following: (1) Tanks must be fabricated from carbon...

  13. 49 CFR 179.102-2 - Chlorine.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 49 Transportation 3 2013-10-01 2013-10-01 false Chlorine. 179.102-2 Section 179.102-2... Tank Car Tanks (Classes DOT-105, 109, 112, 114 and 120) § 179.102-2 Chlorine. (a) Each tank car used to transport chlorine must comply with all of the following: (1) Tanks must be fabricated from carbon...

  14. 49 CFR 179.102-2 - Chlorine.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 49 Transportation 3 2014-10-01 2014-10-01 false Chlorine. 179.102-2 Section 179.102-2... Tank Car Tanks (Classes DOT-105, 109, 112, 114 and 120) § 179.102-2 Chlorine. (a) Each tank car used to transport chlorine must comply with all of the following: (1) Tanks must be fabricated from carbon...

  15. 49 CFR 179.102-2 - Chlorine.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 49 Transportation 2 2010-10-01 2010-10-01 false Chlorine. 179.102-2 Section 179.102-2... Specifications for Pressure Tank Car Tanks (Classes DOT-105, 109, 112, 114 and 120) § 179.102-2 Chlorine. (a) Each tank car used to transport chlorine must comply with all of the following: (1) Tanks must...

  16. 40 CFR 704.45 - Chlorinated terphenyl.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... No. 61788-33-6, comprised of chlorinated ortho-, meta-, and paraterphenyl. (2) Extent of chlorination means the percent by weight of chlorine for each isomer (ortho, meta, and para). (3) Isomeric ratio means the ratios of ortho-, meta-, and parachlorinated terphenyls. (4) Polychlorinated biphenyl...

  17. PREDICTING CHLORINE RESIDUAL LOSSES IN UNLINED METALLIC PIPES (PRESENTATION)

    EPA Science Inventory

    There is substantial evidence that as water moves through a water distribution system its quality can deteriorate through interactions between the bulk phase and the pipe wall. One of the most serious aspects of water quality deterioration, in a network, is the loss of disinfecta...

  18. PREDICTING CHLORINE RESIDUAL LOSSES IN UNLINED METALLIC PIPES (POSTER)

    EPA Science Inventory

    There is substantial evidence that as water moves through a water distribution system its quality can deteriorate through interactions between the bulk phase and the pipe wall. One of the most serious aspects of water quality deterioration, in a network, is the loss of disinfect...

  19. PREDICTING CHLORINE RESIDUAL LOSSES IN UNLINED METALIC PIPES

    EPA Science Inventory

    There is substantial evidence that as water moves through a water distribution system its quality can deteriorate through interactions between the bulk phase and the pipe wall. One of the most serious aspects of water quality deterioration, in a network, is the loss of disinfect...

  20. Disinfectants: Chlorine and chlorine dioxide. (Latest citations from the Life Sciences Collection database). Published Search

    SciTech Connect

    Not Available

    1993-05-01

    The bibliography contains citations concerning the antimicrobial properties of chlorine and chlorine dioxide. The use of chlorine for the inactivation of viruses, bacteria, and fungi in wastewater treatment plants is discussed, including the mode of action and factors influencing inactivation. The use of chlorine dioxide as an alternative to chlorine disinfection in swimming pools and water supplies, and possible adverse effects are also discussed. (Contains a minimum of 157 citations and includes a subject term index and title list.)

  1. Chlorine Abundances in Martian Meteorites

    NASA Technical Reports Server (NTRS)

    Bogard, D.D.; Garrison, D.H.; Park, J.

    2009-01-01

    Chlorine measurements made in martian surface rocks by robotic spacecraft typically give Chlorine (Cl) abundances of approximately 0.1-0.8%. In contrast, Cl abundances in martian meteorites appear lower, although data is limited, and martian nakhlites were also subjected to Cl contamination by Mars surface brines. Chlorine abundances reported by one lab for whole rock (WR) samples of Shergotty, ALH77005, and EET79001 range 108-14 ppm, whereas Cl in nakhlites range 73-1900 ppm. Measurements of Cl in various martian weathering phases of nakhlites varied 0.04-4.7% and reveal significant concentration of Cl by martian brines Martian meteorites contain much lower Chlorine than those measured in martian surface rocks and give further confirmation that Cl in these surface rocks was introduced by brines and weathering. It has been argued that Cl is twice as effective as water in lowering the melting point and promoting melting at shallower martian depths, and that significant Cl in the shergottite source region would negate any need for significant water. However, this conclusion was based on experiments that utilized Cl concentrations more analogous to martian surface rocks than to shergottite meteorites, and may not be applicable to shergottites.

  2. The Chlorine Isotopic Composition Of Lunar UrKREEP

    NASA Technical Reports Server (NTRS)

    Barnes, J. J.; Tartese, R.; Anand, M.; McCubbin, F. M.; Neal, C. R.; Franchi, I. A.

    2016-01-01

    Since the long standing paradigm of an anhydrous Moon was challenged there has been a renewed focus on investigating volatiles in a variety of lunar samples. Numerous studies have examined the abundances and isotopic compositions of volatiles in lunar apatite, Ca5(PO4)3(F,Cl,OH). In particular, apatite has been used as a tool for assessing the sources of H2O in the lunar interior. However, current models for the Moon's formation have yet to fully account for its thermal evolution in the presence of H2O and other volatiles. For ex-ample, in the context of the lunar magma ocean (LMO) model, it is anticipated that chlorine (and other volatiles) should have been concentrated in the late-stage LMO residual melts (i.e., the dregs enriched in incompatible elements such as K, REEs (Rare Earth Elements), and P, collectively called KREEP, and in its primitive form - urKREEP, given its incompatibility in mafic minerals like olivine and pyroxene, which were the dominant phases that crystallized early in the cumulate pile of the LMO. When compared to chondritic meteorites and terrestrial rocks, lunar samples have exotic chlorine isotope compositions, which are difficult to explain in light of the abundance and isotopic composition of other volatile species, especially H, and the current estimates for chlorine and H2O in the bulk silicate Moon (BSM). In order to better understand the processes involved in giving rise to the heavy chlorine isotope compositions of lunar samples, we have performed a comprehensive in situ high precision study of chlorine isotopes in lunar apatite from a suite of Apollo samples covering a range of geochemical characteristics and petrologic types.

  3. BIODEGRADATION OF HYDROCARBON VAPORS IN THE UNSATURATED ZONE

    EPA Science Inventory

    The time-averaged concentration of hydrocarbon and oxygen vapors were measured in the unsaturated zone above the residually contaminated capillary fringe at the U.S. Coast Guard Air Station in Traverse City, Michigan. Total hydrocarbon and oxygen vapor concentrations were observe...

  4. Household Effectiveness vs. Laboratory Efficacy of Point-of-use Chlorination

    PubMed Central

    Levy, Karen; Anderson, Larissa; Robb, Katharine A.; Cevallos, William; Trueba, Gabriel; Eisenberg, Joseph N.S.

    2014-01-01

    Treatment of water at the household level offers a promising approach to combat the global burden of diarrheal diseases. In particular, chlorination of drinking water has been a widely promoted strategy due to persistence of residual chlorine after initial treatment. However, the degree to which chlorination can reduce microbial levels in a controlled setting (efficacy) or in a household setting (effectiveness) can vary as a function of chlorine characteristics, source water characteristics, and household conditions. To gain more understanding of these factors, we carried out an observational study within households in rural communities of northern coastal Ecuador. We found that the efficacy of chlorine treatment under controlled conditions was significantly better than its effectiveness when evaluated both by ability to meet microbiological safety standards and by log reductions. Water treated with chlorine achieved levels of microbial contamination considered safe for human consumption after 24 hours of storage in the household only 39 – 51% of the time, depending on chlorine treatment regimen. Chlorine treatment would not be considered protective against diarrheal disease according to WHO log reduction standards. Factors that explain the observed compromised effectiveness include: source water turbidity, source water baseline contamination levels, and in-home contamination. Water in 38% of the households that had low turbidity source water (< 10 NTU) met the safe water standard as compared with only 17% of the households that had high turbidity source water (> 10 NTU). A 10 MPN/100mL increase in baseline E. coli levels was associated with a 2.2% increase in failure to meet the E. colistandard. Higher mean microbial contamination levels in 54% of household samples in comparison to their matched controls, which is likely the result of in-home contamination during storage. Container characteristics (size of the container mouth) did not influence chlorine

  5. Modeling and kinetic characterization of wastewater disinfection using chlorine and UV irradiation.

    PubMed

    Mounaouer, Brahmi; Abdennaceur, Hassen

    2016-10-01

    Sewage disinfection has the primary objective of inactivating pathogenic organisms to prevent the dissemination of waterborne diseases. This study analyzed individual disinfection, with chlorine alone, ultraviolet radiation alone, and a combined disinfection process (chlorine-UV radiation). Pseudomonas aeruginosa ATCC 15442, Escherichia coli ATCC 11229, Salmonella typhi ATCC 14028, and Clostridium perfringens were selected to evaluate the efficiency of different disinfection processes. The aim of the present study was to characterize the kinetics of chlorine (as NaHOCl) consumption, to evaluate responses of these bacterial species to the chlorination, the ultraviolet (UV) radiation, and the chlorine/UV disinfection processes in secondary wastewater using a batch laboratory reactor. Another target of this work was to study the modeling of the kinetic of water disinfection by chlorination and/or UV irradiation. Two kinetic models (Chick-Watson and Hom) were tested as to ability to scale disinfection of these bacterial species by different ultraviolet and/or chlorine doses. The results of the kinetics of chlorine consumption showed that monochloramines and trichloramines were the most important forms of residual chlorine as compared to free chlorine and dichloramines. The kinetics of inactivation of all examined bacterial strains showed that the application of the model of Hom in its original form was not representative of this kinetics of inactivation. Modification of this model, considering an initial decline of bacteria during the contact of water with chlorine, improved the results of the model. By the same, results revealed that the involved processes of UV irradiation were too complex to be approached by a simplified formulation, even in the case of specific strains of microorganisms and the use of nearly constant UV radiation intensity. In fact, the results have pointed out that the application of the Chick-Watson law is known to be inadequate to describe

  6. Modeling and kinetic characterization of wastewater disinfection using chlorine and UV irradiation.

    PubMed

    Mounaouer, Brahmi; Abdennaceur, Hassen

    2016-10-01

    Sewage disinfection has the primary objective of inactivating pathogenic organisms to prevent the dissemination of waterborne diseases. This study analyzed individual disinfection, with chlorine alone, ultraviolet radiation alone, and a combined disinfection process (chlorine-UV radiation). Pseudomonas aeruginosa ATCC 15442, Escherichia coli ATCC 11229, Salmonella typhi ATCC 14028, and Clostridium perfringens were selected to evaluate the efficiency of different disinfection processes. The aim of the present study was to characterize the kinetics of chlorine (as NaHOCl) consumption, to evaluate responses of these bacterial species to the chlorination, the ultraviolet (UV) radiation, and the chlorine/UV disinfection processes in secondary wastewater using a batch laboratory reactor. Another target of this work was to study the modeling of the kinetic of water disinfection by chlorination and/or UV irradiation. Two kinetic models (Chick-Watson and Hom) were tested as to ability to scale disinfection of these bacterial species by different ultraviolet and/or chlorine doses. The results of the kinetics of chlorine consumption showed that monochloramines and trichloramines were the most important forms of residual chlorine as compared to free chlorine and dichloramines. The kinetics of inactivation of all examined bacterial strains showed that the application of the model of Hom in its original form was not representative of this kinetics of inactivation. Modification of this model, considering an initial decline of bacteria during the contact of water with chlorine, improved the results of the model. By the same, results revealed that the involved processes of UV irradiation were too complex to be approached by a simplified formulation, even in the case of specific strains of microorganisms and the use of nearly constant UV radiation intensity. In fact, the results have pointed out that the application of the Chick-Watson law is known to be inadequate to describe

  7. Characterization and identification of a chlorine-resistant bacterium, Sphingomonas TS001, from a model drinking water distribution system.

    PubMed

    Sun, Wenjun; Liu, Wenjun; Cui, Lifeng; Zhang, Minglu; Wang, Bei

    2013-08-01

    This study describes the identification and characterization of a new chlorine resistant bacterium, Sphingomonas TS001, isolated from a model drinking water distribution system. The isolate was identified by 16s rRNA gene analysis and morphological and physiological characteristics. Phylogenetic analysis indicates that TS001 belongs to the genus Sphingomonas. The model distribution system HPC results showed that, when the chlorine residual was greater than 0.7 mg L(-1), 100% of detected heterotrophic bacteria (HPC) was TS001. The bench-scale inactivation efficiency testing showed that this strain was very resistant to chlorine, and 4 mg L(-1) of chlorine with 240 min retention time provided only approximately 5% viability reduction of TS001. In contrast, a 3-log inactivation (99.9%) was obtained for UV fluencies of 40 mJ cm(-2). A high chlorine-resistant and UV sensitive bacterium, Sphingomonas TS001, was documented for the first time.

  8. Aqueous cleaning of flux residue from solder joints. Final report

    SciTech Connect

    Krska, C.M.

    1992-08-01

    Solder joints have traditionally been cleaned using chlorinated or fluorinated solvents. This study addressed alternate processing. One process involved using a saponifier/water solution to remove rosin flux residues; the other process involved using a water-soluble flux and water to remove the residues. Although both processes were satisfactory, the water-soluble flux with water cleaning proved to be the best.

  9. Aqueous cleaning of flux residue from solder joints

    SciTech Connect

    Krska, C.M.

    1992-08-01

    Solder joints have traditionally been cleaned using chlorinated or fluorinated solvents. This study addressed alternate processing. One process involved using a saponifier/water solution to remove rosin flux residues; the other process involved using a water-soluble flux and water to remove the residues. Although both processes were satisfactory, the water-soluble flux with water cleaning proved to be the best.

  10. Environmental factors regulating soil organic matter chlorination

    NASA Astrophysics Data System (ADS)

    Svensson, Teresia; Montelius, Malin; Reyier, Henrik; Rietz, Karolina; Karlsson, Susanne; Lindberg, Cecilia; Andersson, Malin; Danielsson, Åsa; Bastviken, David

    2016-04-01

    Natural chlorination of organic matter is common in soils. Despite the widespread abundance of soil chlorinated soil organic matter (SOM), frequently exceeding soil chloride abundance in surface soils, and a common ability of microorganisms to produce chlorinated SOM, we lack fundamental knowledge about dominating processes and organisms responsible for the chlorination. To take one step towards resolving the terrestrial chlorine (Cl) puzzle, this study aims to analyse how environmental factors influence chlorination of SOM. Four factors were chosen for this study: soil moisture (W), nitrogen (N), chloride (Cl) and organic matter quality (C). These factors are all known to be important for soil processes. Laboratory incubations with 36Cl as a Cl tracer were performed in a two soil incubation experiments. It was found that addition of chloride and nitrogen seem to hamper the chlorination. For the C treatment, on the other hand, the results show that chlorination is enhanced by increased availability of labile organic matter (glucose and maltose). Even higher chlorination was observed when nitrogen and water were added in combination with labile organic matter. The effect that more labile organic matter strongly stimulated the chlorination rates was confirmed by the second separate experiment. These results indicate that chlorination was not primarily a way to cut refractory organic matter into digestible molecules, representing one previous hypothesis, but is related with microbial metabolism in other ways that will be further discussed in our presentation.

  11. Distribution and chemical fate of chlorine dioxide gas during sanitation of tomatoes and cantaloupe

    Technology Transfer Automated Retrieval System (TEKTRAN)

    A series of studies was conducted to establish the 1) distribution and chemical fate of 36-ClO2 on tomatoes and cantaloupe; and 2) the magnitude of residues in kilogram quantities of tomatoes and cantaloupe sanitized with a slow-release chlorine dioxide formulation. Tomatoes and cantaloupe were resp...

  12. Chlorine signal attenuation in concrete.

    PubMed

    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.

  13. Detection of chlorinated aromatic compounds

    DOEpatents

    Ekechukwu, Amy A.

    1996-01-01

    A method for making a composition for measuring the concentration of chloated aromatic compounds in aqueous fluids, and an optical probe for use with the method. The composition comprises a hydrophobic polymer matrix, preferably polyamide, with a fluorescent indicator uniformly dispersed therein. The indicator fluoresces in the presence of the chlorinated aromatic compounds with an intensity dependent on the concentration of these compounds in the fluid of interest, such as 8-amino-2-naphthalene sulfonate. The probe includes a hollow cylindrical housing that contains the composition in its distal end. The probe admits an aqueous fluid to the probe interior for exposure to the composition. An optical fiber transmits excitation light from a remote source to the composition while the indicator reacts with chlorinated aromatic compounds present in the fluid. The resulting fluorescence light signal is reflected to a second optical fiber that transmits the light to a spectrophotometer for analysis.

  14. Microbial based chlorinated ethene destruction

    DOEpatents

    Bagwell, Christopher E.; Freedman, David L.; Brigmon, Robin L.; Bratt, William B.; Wood, Elizabeth A.

    2009-11-10

    A mixed culture of Dehalococcoides species is provided that has an ability to catalyze the complete dechlorination of polychlorinated ethenes such as PCE, TCE, cDCE, 1,1-DCE and vinyl chloride as well as halogenated ethanes such as 1,2-DCA and EDB. The mixed culture demonstrates the ability to achieve dechlorination even in the presence of high source concentrations of chlorinated ethenes.

  15. Coal desulfurization by aqueous chlorination

    NASA Technical Reports Server (NTRS)

    Kalvinskas, J. J.; Vasilakos, N.; Corcoran, W. H.; Grohmann, K.; Rohatgi, N. K. (Inventor)

    1982-01-01

    A method of desulfurizing coal is described in which chlorine gas is bubbled through an aqueous slurry of coal at low temperature below 130 degrees C., and at ambient pressure. Chlorinolysis converts both inorganic and organic sulfur components of coal into water soluble compounds which enter the aqueous suspending media. The media is separated after chlorinolysis and the coal dechlorinated at a temperature of from 300 C to 500 C to form a non-caking, low-sulfur coal product.

  16. Bacterial dehalorespiration with chlorinated benzenes.

    PubMed

    Adrian, L; Szewzyk, U; Wecke, J; Görisch, H

    2000-11-30

    Chlorobenzenes are toxic, highly persistent and ubiquitously distributed environmental contaminants that accumulate in the food chain. The only known microbial transformation of 1,2,3,5-tetrachlorobenzene (TeCB) and higher chlorinated benzenes is the reductive dechlorination to lower chlorinated benzenes under anaerobic conditions observed with mixed bacterial cultures. The lower chlorinated benzenes can subsequently be mineralized by aerobic bacteria. Here we describe the isolation of the oxygen-sensitive strain CBDB1, a pure culture capable of reductive dechlorination of chlorobenzenes. Strain CBDB1 is a highly specialized bacterium that stoichiometrically dechlorinates 1,2,3-trichlorobenzene (TCB), 1,2,4-TCB, 1,2,3,4-TeCB, 1,2,3,5-TeCB and 1,2,4,5-TeCB to dichlorobenzenes or 1,3,5-TCB. The presence of chlorobenzene as an electron acceptor and hydrogen as an electron donor is essential for growth, and indicates that strain CBDB1 meets its energy needs by a dehalorespiratory process. According to their 16S rRNA gene sequences, strain CBDB1, Dehalococcoides ethenogenes and several uncultivated bacteria form a new bacterial cluster, of which strain CBDB1 is the first, so far, to thrive on a purely synthetic medium.

  17. UV/chlorine process for ammonia removal and disinfection by-product reduction: comparison with chlorination.

    PubMed

    Zhang, Xinran; Li, Weiguang; Blatchley, Ernest R; Wang, Xiaoju; Ren, Pengfei

    2015-01-01

    The combined application of UV irradiation at 254 nm and chlorination (UV/chlorine process) was investigated for ammonia removal in water treatment. The UV/chlorine process led to higher ammonia removal with less chlorine demand, as compared to breakpoint chlorination. Chlorination of NH₃ led to NH₂Cl formation in the first step. The photolysis of NH₂Cl and radical- mediated oxidation of ammonia appeared to represent the main pathways for ammonia removal. The trivalent nitrogen of ammonia was oxidized, presumably by reactions with aminyl radicals and chlorine radicals. Measured products included NO₃⁻and NO₂⁻; it is likely that N₂ and N₂O were also generated. In addition, UV irradiation appeared to have altered the reactivity of NOM toward free chlorine. The UV/chlorine process had lower chlorine demand, less C-DBPs (THMs and HAAs), but more HANs than chlorination. These results indicate that the UV/chlorine process could represent an alternative to conventional breakpoint chlorination for ammonia-containing water, with several advantages in terms of simplicity, short reaction time, and reduced chemical dosage.

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

    PubMed

    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. PMID:27441859

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

    PubMed

    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.

  20. Chlorine disinfection of grey water for reuse: effect of organics and particles.

    PubMed

    Winward, Gideon P; Avery, Lisa M; Stephenson, Tom; Jefferson, Bruce

    2008-01-01

    Adequate disinfection of grey water prior to reuse is important to prevent the potential transmission of disease-causing microorganisms. Chlorine is a widely utilised disinfectant and as such is a leading contender for disinfection of grey water intended for reuse. This study examined the impact of organics and particles on chlorine disinfection of grey water, measured by total coliform inactivation. The efficacy of disinfection was most closely linked with particle size. Larger particles shielded total coliforms from inactivation and disinfection efficacy decreased with increasing particle size. Blending to extract particle-associated coliforms (PACs) following chlorine disinfection revealed that up to 91% of total coliforms in chlorinated grey water were particle associated. The organic concentration of grey water affected chlorine demand but did not influence the disinfection resistance of total coliforms when a free chlorine residual was maintained. Implications for urban water reuse are discussed and it is recommended that grey water treatment systems target suspended solids removal to ensure removal of PACs prior to disinfection.

  1. Bacterial Community Shift Drives Antibiotic Resistance Promotion during Drinking Water Chlorination.

    PubMed

    Jia, Shuyu; Shi, Peng; Hu, Qing; Li, Bing; Zhang, Tong; Zhang, Xu-Xiang

    2015-10-20

    For comprehensive insights into the effects of chlorination, a widely used disinfection technology, on bacterial community and antibiotic resistome in drinking water, this study applied high-throughput sequencing and metagenomic approaches to investigate the changing patterns of antibiotic resistance genes (ARGs) and bacterial community in a drinking water treatment and distribution system. At genus level, chlorination could effectively remove Methylophilus, Methylotenera, Limnobacter, and Polynucleobacter, while increase the relative abundance of Pseudomonas, Acidovorax, Sphingomonas, Pleomonas, and Undibacterium in the drinking water. A total of 151 ARGs within 15 types were detectable in the drinking water, and chlorination evidently increased their total relative abundance while reduced their diversity in the opportunistic bacteria (p < 0.05). Residual chlorine was identified as the key contributing factor driving the bacterial community shift and resistome alteration. As the dominant persistent ARGs in the treatment and distribution system, multidrug resistance genes (mainly encoding resistance-nodulation-cell division transportation system) and bacitracin resistance gene bacA were mainly carried by chlorine-resistant bacteria Pseudomonas and Acidovorax, which mainly contributed to the ARGs abundance increase. The strong correlation between bacterial community shift and antibiotic resistome alteration observed in this study may shed new light on the mechanism behind the chlorination effects on antibiotic resistance.

  2. Hydrocarbon release investigations in Missouri

    SciTech Connect

    Fels, J.B.

    1996-09-01

    Hydrocarbon releases are among the most common environmental problems in Missouri, as well as across the country. Old, unprotected underground storage tanks and buried piping from the tanks to pumps are notorious sources of petroleum contamination at LUST (leaking underground storage tank) sites. Missouri has an estimated 5000 LUST sites across the state with the majority being simple spills into clay-rich soils or into a shallow perched water system. However, in the southern half of the state, where residual soils and karst bedrock are not conducive to trapping such releases, significant groundwater supplies are at risk. This article discusses the process used to identify the source of contamination.

  3. Observations of interstellar chlorine and phosphorus

    NASA Technical Reports Server (NTRS)

    Jura, M.; York, D. G.

    1978-01-01

    Copernicus observations of interstellar Cl I, Cl II, and P II UV lines toward 10 stars are reported. Column densities are estimated for each species, and upper limits are computed for HCl column densities. Derivation of the gas-phase abundances of chlorine and phosphorus indicates that the averages of both the chlorine and the phosphorus logarithmic abundances relative to hydrogen are between 5.0 and 5.1. It is suggested that interstellar chlorine may be depleted by about a factor of 3 relative to the solar abundance and that interstellar phosphorus is depleted by a factor of 2 to 3. The results are shown to support the prediction that chlorine is ionized in regions containing primarily atomic oxygen and is neutral in regions where there is a significant amount of molecular hydrogen. The photoionization rate of neutral chlorine toward 15 Mon is estimated, and it is concluded that most chlorine is contained within the gas phase.

  4. [Chlorinate solvents natural biodegradation in shallow groundwater].

    PubMed

    He, Jiang-tao; Li, Ye; Liu, Shi; Chen, Hong-han

    2005-03-01

    Chlorinated solvents contaminations are most popular in shallow groundwater. A serious local groundwater contamination of chlorinated solvents is founded in a north city of China during the organic pollution investigation. On the basis of the available data and the determining methods of chlorinated solvents biodegradation in groundwater under natural conditions, research on chlorinated solvents biodegrading potential is carried out. The results show that the ground water environment parameters, Eh and pH of the groundwater, indirect sign of biodegradation, i.e. NO3- changing, and concentration variation of biodegradation intermediate products of PCE and TCE all proved that chlorinated solvents can be degraded by microorganism in groundwater. The results of simulating experiment also reveal that, co-metabolism biodegradation of chlorinated solvent was possible under the groundwater circumstances in this sample. Therefore, admitting there is biotransformation from PCE to TCE can explain the present situation more reasonably.

  5. pH fluorescent probes: chlorinated fluoresceins.

    PubMed

    Ge, Feng-Yan; Chen, Li-Gong

    2008-01-01

    A series of regiospecific chlorinated fluoresceins have been synthesized by the reaction of the regiospecific chlorinated resorcinols with chlorinated phthalic anhydride. The regioisomers were successfully separated by chromatography. The photophysical properties of the obtained chlorinated fluoresceins were examined and found their absorption and emission maxima at long wavelength with high fluorescence quantum yield. Especially, pH-dependent properties of chlorinated fluoresceins have been studied in detail. These compounds show strongly pH-sensitive range of 3.5-7.0, and have lower pK (a) values than fluorescein. Furthermore, their fluorescent intensity could reach the maximum in the physiological environment of pH range 6.8-7.4. Due to higher fluorescence quantum yield and lower pK (a) values, chlorinated fluoresceins will be expected to be used as excellent pH fluorescent probes for pH measurement of the acidic cell.

  6. Hydrocarbon product stripping

    SciTech Connect

    Harandi, M.N.; Owen, H.; Siuta, M.T.

    1989-04-18

    A method is described for stripping light gasiform components from the liquid effluent of a catalytic hydrodesulfurization process, which comprises separating the liquid effluent containing relatively low boiling hydrocarbon components, relatively high boiling hydrocarbon components, hydrogen, and hydrogen sulfide.

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

    PubMed

    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.

  8. Vanadium-catalyzed chlorination under molecular oxygen.

    PubMed

    Moriuchi, Toshiyuki; Fukui, Yasuhiro; Kato, Satoshi; Kajikawa, Tomomi; Hirao, Toshikazu

    2015-06-01

    A catalytic chlorination of ketones was performed by using a vanadium catalyst in the presence of Bu4NI and AlCl3 under atmospheric molecular oxygen. This catalytic chlorination could be applied to the chlorination of alkenes to give the corresponding vic-dichlorides. AlCl3 was found to serve as both a Lewis acid and a chloride source to induce the facile chlorination. A combination of Bu4NI and AlI3 in the presence of a vanadium catalyst under atmospheric molecular oxygen induced the iodination of ketones.

  9. Foaming of mixtures of pure hydrocarbons

    NASA Technical Reports Server (NTRS)

    Robinson, J. V.; Woods, W. W.

    1950-01-01

    Mixtures of pure liquid hydrocarbons are capable of foaming. Nine hydrocarbons were mixed in pairs, in all possible combinations, and four proportions of each combination. These mixtures were sealed in glass tubes, and the foaming was tested by shaking. Mixtures of aliphatic with other aliphatic hydrocarbons, or of alkyl benzenes with other alkyl benzenes, did not foam. Mixtures of aliphatic hydrocarbons with alkyl benzenes did foam. The proportions of the mixtures greatly affected the foaming, the maximum foaming of 12 of 20 pairs being at the composition 20 percent aliphatic hydrocarbon, 80 percent alkyl benzene. Six seconds was the maximum foam lifetime of any of these mixtures. Aeroshell 120 lubricating oil was fractionated into 52 fractions and a residue by extraction with acetone in a fractionating extractor. The index of refraction, foam lifetime, color, and viscosity of these fractions were measured. Low viscosity and high index fractions were extracted first. The viscosity of the fractions extracted rose and the index decreased as fractionation proceeded. Foam lifetimes and color were lowest in the middle fractions. Significance is attached to the observation that none of the foam lifetimes of the fractions or residue is as high as the foam lifetime of the original Aeroshell, indicating that the foaming is not due to a particular foaming constituent, but rather to the entire mixture.

  10. Chlorine-Susceptible and Chlorine-Resistant Type 021N Bacteria Occurring in Bulking Activated Sludges

    PubMed Central

    Séka, M. A.; Kalogo, Y.; Hammes, F.; Kielemoes, J.; Verstraete, W.

    2001-01-01

    Two filamentous bacteria causing bulking in two activated sludges were examined. Investigations using morphological features, staining techniques, and fluorescent in situ hybridization identified both filaments as type 021N. However, an examination of the effect of chlorine on the sludges revealed a chlorine-susceptible type 021N in one sludge and a chlorine-resistant type 021N in the other. PMID:11679359

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

    PubMed

    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. A kinetics investigation of several reactions involving chlorine containing compounds

    NASA Technical Reports Server (NTRS)

    Davis, D. D.

    1978-01-01

    The technique of flash photolysis-resonance fluorescence was utilized to study nine reactions of stratospheric importance. The tropospheric degradation reactions of seven halogenated hydrocarbons were studied to assess their possible influx into the stratosphere. There are reactions of either Cl, OH, or O(3P) species with hydrogenated species, O3 or chlorinated compounds. Apart from the kinetic measurements, the quantum yield for the production of O(1D) from O3 in the crucial wavelength region of 293 to 316.5 nm was studied by utilizing a narrow wavelength laser as the photolysis source. The product formation was monitored by measuring the fluorescence of NO2 formed through O(1D) reaction with N2O followed by NO reaction with O3 to give NO2.

  13. Chlorine fate and transport in drinking water distribution systems: Results from experimental and modeling studies

    NASA Astrophysics Data System (ADS)

    Clark, Robert M.

    2011-12-01

    It has become generally accepted that water quality can deteriorate in a distribution system through microbiological and chemical reactions in the bulk phase and/or at the pipe wall. The most serious aspect of water quality deterioration in a network is the loss of the disinfectant residual that can weaken the barrier against microbial contamination. Studies have suggested that one factor contributing to the loss of disinfectant residuals is the reaction between bulk phase disinfectants and pipe wall material. Free chlorine loss in corroded metal and PVC pipes, subject to changes in velocity, was assessed during an experiment conducted under controlled conditions in a specially constructed pipe loop located at the US Environmental Protection Agency's (EPA's) Test and Evaluation (T&E) Facility in Cincinnati, Ohio (USA). These studies demonstrated that in older unlined metal pipes, the loss of chlorine residual increases with velocity but that wall demand in PVC was negligible.

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

    PubMed

    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.

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

    PubMed

    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

  16. Decontamination of Pangasius fish (Pangasius hypophthalmus) with chlorine or peracetic acid in the laboratory and in a Vietnamese processing company.

    PubMed

    Tong Thi, Anh Ngoc; Sampers, Imca; Van Haute, Sam; Samapundo, Simbarashe; Ly Nguyen, Binh; Heyndrickx, Marc; Devlieghere, Frank

    2015-09-01

    This study evaluated the decontamination of Pangasius fillets in chlorine or peracetic acid treated wash water. First, the decontamination efficacy of the washing step with chlorinated water applied by a Vietnamese processing company during trimming of Pangasius fillets was evaluated and used as the basis for the experiments performed on a laboratory scale. As chlorine was only added at the beginning of the batch and used continuously without renewal for 239min; a rapid increase of the bacterial counts and a fast decrease of chlorine in the wash water were found. This could be explained by the rapid accumulation of organic matter (ca. 400mg O2/L of COD after only 24min). Secondly, for the experiments performed on a laboratory scale, a single batch approach (one batch of wash water for treating a fillet) was used. Chlorine and PAA were evaluated at 10, 20, 50 and 150ppm at contact times of 10, 20 and 240s. Washing with chlorine and PAA wash water resulted in a reduction of Escherichia coli on Pangasius fish which ranged from 0-1.0 and 0.4-1.4logCFU/g, respectively while less to no reduction of total psychrotrophic counts, lactic acid bacteria and coliforms on Pangasius fish was observed. However, in comparison to PAA, chlorine was lost rapidly. As an example, 53-83% of chlorine and 15-17% of PAA were lost after washing for 40s (COD=238.2±66.3mg O2/L). Peracetic acid can therefore be an alternative sanitizer. However, its higher cost will have to be taken into consideration. Where (cheaper) chlorine is used, the processors have to pay close attention to the residual chlorine level, pH and COD level during treatment for optimal efficacy. PMID:26058007

  17. Decontamination of Pangasius fish (Pangasius hypophthalmus) with chlorine or peracetic acid in the laboratory and in a Vietnamese processing company.

    PubMed

    Tong Thi, Anh Ngoc; Sampers, Imca; Van Haute, Sam; Samapundo, Simbarashe; Ly Nguyen, Binh; Heyndrickx, Marc; Devlieghere, Frank

    2015-09-01

    This study evaluated the decontamination of Pangasius fillets in chlorine or peracetic acid treated wash water. First, the decontamination efficacy of the washing step with chlorinated water applied by a Vietnamese processing company during trimming of Pangasius fillets was evaluated and used as the basis for the experiments performed on a laboratory scale. As chlorine was only added at the beginning of the batch and used continuously without renewal for 239min; a rapid increase of the bacterial counts and a fast decrease of chlorine in the wash water were found. This could be explained by the rapid accumulation of organic matter (ca. 400mg O2/L of COD after only 24min). Secondly, for the experiments performed on a laboratory scale, a single batch approach (one batch of wash water for treating a fillet) was used. Chlorine and PAA were evaluated at 10, 20, 50 and 150ppm at contact times of 10, 20 and 240s. Washing with chlorine and PAA wash water resulted in a reduction of Escherichia coli on Pangasius fish which ranged from 0-1.0 and 0.4-1.4logCFU/g, respectively while less to no reduction of total psychrotrophic counts, lactic acid bacteria and coliforms on Pangasius fish was observed. However, in comparison to PAA, chlorine was lost rapidly. As an example, 53-83% of chlorine and 15-17% of PAA were lost after washing for 40s (COD=238.2±66.3mg O2/L). Peracetic acid can therefore be an alternative sanitizer. However, its higher cost will have to be taken into consideration. Where (cheaper) chlorine is used, the processors have to pay close attention to the residual chlorine level, pH and COD level during treatment for optimal efficacy.

  18. Chlorinated Withanolides from Withania somnifera

    PubMed Central

    Tong, Xiaoqin; Zhang, Huaping; Timmermann, Barbara N.

    2011-01-01

    A chlorinated withanolide, 6α-chloro-5β,17α-dihydroxywithaferin A (1), and nine known withanolides, 6α-chloro-5β-hydroxywithaferin A (2), (22R)-5β-formyl-6β,27-dihydroxy-1-oxo-4-norwith-24-enolide, withaferin A, 2,3-dihydrowithaferin A, 3-methoxy-2,3-dihydrowithaferin A, 2,3-didehydrosomnifericin, withanone, withanoside IV and withanoside X, were isolated from Withania somnifera (Solanaceae). All structures were elucidated on the basis of spectroscopic methods (IR, HRESIMS, 1D/2D NMR). X-ray crystallography confirmed the absolute configuration of 1. PMID:22125584

  19. A comparison of two systems for chlorinating water in rural Honduras.

    PubMed

    Henderson, Amy K; Sack, R Bradley; Toledo, Erick

    2005-09-01

    This study investigated a small subset of the two community water-disinfection systems--hypochlorinators and tablet feeders-in rural Honduras. Levels of residual chlorine were assessed at three locations within the distribution system: the tank, the proximal house, and the distal house. The levels of residual chlorine were compared with the standard guidelines set by the Pan American Health Organization and the International Rural Water Association for potable water that require a minimum of 1.0 (tank), 0.5 (proximal house), and 0.2 (distal house) ppm for each location. The levels of residual chlorine were also compared across systems, e.g. hypochlorinators to tablet feeders. At the tank and proximal house, tablet feeders had significantly higher mean values for levels of residual chlorine (measured in ppm) than hypochlorinators (tank: 1.20 vs 0.67; proximal house: 0.44 vs 0.32, p < 0.001 for both) with no significant difference at the distal house (0.16 vs 0.16). At the tank and proximal house, tablet feeders were more likely to meet recommended standards than hypochlorinators (90.3% vs 13.3%, p < 0.0001 and 41.3% vs 23.7%, p < 0.0001) with a smaller difference seen at the distal house (30.6% vs 27.1%, p = 0.24). The apparent dichotomy in chlorine levels of tablet feeders (e.g. between tank/proximal house and distal house) is discussed. The results suggest that tablet feeders may be more effective than hypochlorinators in supplying clean water in rural, resource-poor settings and possibly serve as an alternative technology for water disinfection. Further research on techniques for empowering and building capacity within community water boards will help organize and introduce sustainable water systems in developing countries.

  20. A comparison of two systems for chlorinating water in rural Honduras.

    PubMed

    Henderson, Amy K; Sack, R Bradley; Toledo, Erick

    2005-09-01

    This study investigated a small subset of the two community water-disinfection systems--hypochlorinators and tablet feeders-in rural Honduras. Levels of residual chlorine were assessed at three locations within the distribution system: the tank, the proximal house, and the distal house. The levels of residual chlorine were compared with the standard guidelines set by the Pan American Health Organization and the International Rural Water Association for potable water that require a minimum of 1.0 (tank), 0.5 (proximal house), and 0.2 (distal house) ppm for each location. The levels of residual chlorine were also compared across systems, e.g. hypochlorinators to tablet feeders. At the tank and proximal house, tablet feeders had significantly higher mean values for levels of residual chlorine (measured in ppm) than hypochlorinators (tank: 1.20 vs 0.67; proximal house: 0.44 vs 0.32, p < 0.001 for both) with no significant difference at the distal house (0.16 vs 0.16). At the tank and proximal house, tablet feeders were more likely to meet recommended standards than hypochlorinators (90.3% vs 13.3%, p < 0.0001 and 41.3% vs 23.7%, p < 0.0001) with a smaller difference seen at the distal house (30.6% vs 27.1%, p = 0.24). The apparent dichotomy in chlorine levels of tablet feeders (e.g. between tank/proximal house and distal house) is discussed. The results suggest that tablet feeders may be more effective than hypochlorinators in supplying clean water in rural, resource-poor settings and possibly serve as an alternative technology for water disinfection. Further research on techniques for empowering and building capacity within community water boards will help organize and introduce sustainable water systems in developing countries. PMID:16262025

  1. Ether and hydrocarbon production

    SciTech Connect

    Harandi, M.N.; Owen, H.

    1991-03-19

    This patent describes a continuous process for converting lower aliphatic alkanol and olefinic hydrocarbon to alkyl tertiary-alkyl ethers and C{sub 5} + gasoline boiling range hydrocarbons. It comprises contacting alkanol and a light olefinic hydrocarbon stream rich in isobutylene and other C{sub 4} isomeric hydrocarbons under iso-olefin etherification conditions in an etherification reaction zone containing acid etherification catalyst; separating etherification effluent to recover a light stream comprising unreacted alkanol and light olefinic hydrocarbon and a liquid product stream containing alkyl tertiary-butyl ether; and contacting the light stream with acidic, medium pore metallosilicate catalyst under alkanol and hydrocarbon conversion conditions whereby C{sub 5} + gasoline boiling range hydrocarbons are produced.

  2. Induction of hepatic cytochrome P450 isozymes, benzo(a)pyrene metabolism and DNA binding following exposure to polycyclic aromatic hydrocarbon residues generated during repeated fish fried oil in rats

    SciTech Connect

    Pandey, Manoj K.; Yadav, Sanjay; Parmar, Devendra; Das, Mukul . E-mail: mditrc@rediffmail.com

    2006-06-01

    In the present study the effect of repeated fish fried oil (RFFO) and its extract (RFFE) on hepatic cytochrome P450 (CYP) isozymes, benzo(a)pyrene (BP) metabolism and DNA adduct formation was undertaken. HPLC analysis of RFFO showed the presence of several polycyclic aromatic hydrocarbons. CYP in microsomes from control and RFFO-treated animals showed a peak at 450 nm; however, a shift of 2 nm in the SORET region along with significant induction was observed in microsomes prepared from 3-methylcholanthrene (MC)- and RFFE-treated animals. Activities of hepatic ethoxyresorufin-O-deethylase, methoxyresorufin-O-deethylase, aryl hydrocarbon hydroxylase and erythromycin-N-demethylase were found to be significantly (P < 0.05) induced following exposure of RFFE, whereas none of these enzymes were altered in RFFO-treated group. Immunoblot analysis revealed that RFFE and MC were potent inducers of CYP1A1, 1A1/2 and 3A1 isozymes, where as RFFO showed no change in these protein levels. RT-PCR analysis showed induction of cDNA of CYP1A1 and CYP3A1 by RFFE treatment. Hepatic microsomes prepared from RFFE exposed animals enhanced BP metabolism with a concomitant increase in the relative proportion of BP 7,8-diol. Hepatic microsomes prepared from animals pretreated with RFFE and MC significantly enhanced the binding of [{sup 3}H]-BP to calf thymus DNA. The overall results suggest that exposure to RFFE may induce hepatic CYP isozymes thereby producing enhanced reactive metabolites with a potential to bind with DNA that may result in cancer.

  3. Chlorination-induced genotoxicity in the mussel Perna viridis: assessment by single cell gel electrophoresis (comet) assay.

    PubMed

    Chavan, Pooja; Kumar, Rajesh; Kirubagaran, Ramalingam; Venugopalan, Vayalam P

    2016-08-01

    Mussels are important fouling organisms in the cooling water systems of coastal power plants. Continuous low-dose chlorination (CLDC) is being practiced as an effective method to control mussel biofouling in power plant cooling water systems. CLDC effectively controls mussel fouling by discouraging larval settlement rather than by killing the larvae or adults. Mussels are an integral part of the natural benthic community in the receiving water body where the coolant water is discharged. Hence, from a toxicological point of view, they can serve as both target and non-target organisms. Previous researchers have indicated that chlorine residual, rather than elevated temperature, can be the major stress factor in the effluents released from coastal power plants. However, very little data are available on the sub-lethal effects of low level chlorination on representative benthic fauna. In this study, we used native and transplanted mussels (Perna viridis) to study lethal and sub-lethal effects of chlorination in the cooling water circuit of an operating power plant. Experiments involving comet assay suggested that CLDC can cause DNA damage in treated mussels. However, activation of DNA repair appeared to get initiated after the accrued damage reached a threshold. The results indicate that, at chlorine residual levels observed at the discharge point, exposure to chlorinated effluents is unlikely to cause significant genetic damage to mussels in the recipient water body. PMID:27155389

  4. Chemotaxis of Pseudomonas putida toward chlorinated benzoates

    SciTech Connect

    Harwood, C.S.; Parales, R.E.; Dispensa, M. )

    1990-05-01

    The chlorinated aromatic acids 3-chlorobenzoate and 4-chlorobenzoate are chemoattractants for Pseudomonas putida PRS2000. These compounds are detected by a chromosomally encoded chemotactic response to benzoate which is inducible by {beta}-ketoadipate, and intermediate of benzoate catabolism. Plasmid pAC27, encoding enzymes for 3-chlorobenzoate degradation, does not appear to carry genes for chemotaxis toward chlorinated compounds.

  5. Toxicity of chlorine to zebrafish embryos.

    PubMed

    Kent, Michael L; Buchner, Cari; Barton, Carrie; Tanguay, Robert L

    2014-01-16

    Surface disinfection of fertilized fish eggs is widely used in aquaculture to reduce extraovum pathogens that may be released from brood fish during spawning, and this is routinely used in zebrafish Danio rerio research laboratories. Most laboratories use approximately 25 to 50 ppm unbuffered chlorine solution for 5 to 10 min. Treatment of embryos with chlorine has significant germicidal effects for many Gram-negative bacteria, viruses, and trophozoite stages of protozoa, but is less effective against cyst or spore stages of protozoa and certain Mycobacterium spp. Therefore, we evaluated the toxicity of unbuffered and buffered chlorine solutions to embryos exposed at 6 or 24 h post-fertilization (hpf) to determine whether higher concentrations can be used for treating zebrafish embryos. Most of our experiments entailed using an outbred line (5D), with both mortality and malformations as endpoints. We found that 6 hpf embryos consistently were more resistant than 24 hpf embryos to the toxic effects of chlorine. Chlorine is more toxic and germicidal at lower pH, and chlorine causes elevated pH. Consistent with this, we found that unbuffered chlorine solutions (pH ca. 8-9) were less toxic at corresponding concentrations than solutions buffered to pH 7. Based on our findings here, we recommend treating 6 hpf embryos for 10 min and 24 hpf embryos for 5 min with unbuffered chlorine solution at 100 ppm.

  6. Factors Regulating Soil Organic Matter Chlorination

    NASA Astrophysics Data System (ADS)

    Svensson, T.; Gustavsson, M.; Reyier, H.; Rietz, K.; Karlsson, S.; Göransson, C.; Andersson, M.; Öberg, G.; Bastviken, D.

    2013-12-01

    Natural chlorination of organic matter is a common process in various soils. Despite the widespread abundance of soil organic chlorine, knowledge on the processes and regulation of soil organic matter chlorination are modest. The purpose of this study is to elucidate how environmental factors may influence chlorination of organic matter in soil. Four factors were chosen for this study; water content, and nitrogen, organic carbon, and chloride concentrations. The variables are all known in different ways as important for microbes and transformation of chlorine in soil. The soil was collected from 5-15 cm depth in a coniferous forest southeast of Sweden. To test how the selected factors influenced chlorination of organic matter, we used soil laboratory incubations using 36Cl-chloride as a radioisotopic marker. A multivariate factorial design with two levels of i) soil moisture, ii) chloride amendment, iii) nitrogen amendment, and iv) glucose and maltose addition was used to simultaneously test for possible combination effects for all factors. A known radioactivity of 36chloride was added to the soil samples and incubated with four different factor treatments during an incubation period of 15 and 60 days. This presentation will discuss the results of this study including what combination of factors enhanced or hampered chlorination and thereby discuss previous observed variability of organic chlorine and chloride in soil.

  7. 46 CFR 151.50-31 - Chlorine.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... GUARD, DEPARTMENT OF HOMELAND SECURITY (CONTINUED) CERTAIN BULK DANGEROUS CARGOES BARGES CARRYING BULK LIQUID HAZARDOUS MATERIAL CARGOES Special Requirements § 151.50-31 Chlorine. (a) Chlorine barges... as complying with this part. (b) Design and construction of cargo tanks. (1) The cargo tanks...

  8. Radiochemical analysis of chlorine-36

    NASA Astrophysics Data System (ADS)

    Rodríguez, M.; Piña, G.; Lara, E.

    2006-01-01

    The radioactive chlorine isotope, 36Cl, decays with a half-life of 3×105 years by emitting a beta particle (98 %) and by electron capture. The aim of this paper is to propose a radiochemical separation method of 36Cl from the other beta-gamma emitters present in low and medium radioactive wastes such as spent ion exchange resins and evaporator concentrates, that arise from Nuclear Power Plants and particularly in the wastes that come from decommissioning activities of graphite reactors, in order to provide data for 36Cl inventory calculations. The separation method proposed is based on an oxidation technique where chlorine is trapped by NaOH. 36Cl beta emissions are measured by liquid scintillation counting by the dual label technique in order to avoid the contamination produced by 14C which is also trapped by NaOH and which is the main contaminant present in graphite samples. The sensitivity of this method is sufficient to achieve the needed thresholds for the radiological characterization of the radioactive materials to which this method can be applied.

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

    SciTech Connect

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

    1990-05-01

    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% inactivation after 1 h, while 80 ppm of chlorine and 80 ppm of monochloramine required approximately 90 min for 90% inactivation. The data indicate that C. parvum oocysts are 30 times more resistant to ozone and 14 times more resistant to chlorine dioxide than Giardia cysts exposed to these disinfectants under the same conditions. With the possible exception of ozone, the use of disinfectants alone should not be expected to inactivate C. parvum oocysts in drinking water.

  10. Chlorine

    MedlinePlus

    ... gas are inhaled. Fluid in the lungs (pulmonary edema) that may be delayed for a few hours ... problems such as fluid in the lungs (pulmonary edema) following the initial exposure. How people can protect ...

  11. Spatial distribution, temporal variation and risks of parabens and their chlorinated derivatives in urban surface water in Beijing, China.

    PubMed

    Li, Wenhui; Gao, Lihong; Shi, Yali; Wang, Yuan; Liu, Jiemin; Cai, Yaqi

    2016-01-01

    The occurrence and distribution of 13 target compounds, including eight parabens, four chlorinated parabens and p-hydroxybenzoic acid (PHBA), were detected in surface water samples at 35 sampling sites in the Beijing River system, China. The surface water samples were collected from the main rivers and lakes in the urban area monthly from July 2013 to June 2014 (except the frozen period). Laboratory analyses revealed that parabens were ubiquitous in the surface water of Beijing. PHBA was the predominant compound in the surface water samples, with the average concentration of 239ngL(-1), followed by the total amount of chlorinated parabens (average 50.1ng/L) and parabens (average 44.3ng/L). It is noteworthy that octylparaben with longer chain was firstly detected in the surface water. Significant difference was observed for paraben concentrations from different sampling sites, and the highest level of parabens was found in the Xiaotaihou River, which was mainly due to the untreated sewage discharge. Seasonal variation of target compounds in the urban surface water was also studied, and parabens exhibited a different temporal variation from chlorinated derivatives. A combination of factors including high residual chlorine level and water temperature as well as intense ultraviolet radiation might enhance the persistence of chlorinated parabens in chlorinated water during the wet season. Risk assessment showed that parabens and their chlorinated derivatives are not likely to produce biological effects on aquatic ecosystems at current levels in the surface water of Beijing.

  12. Biodegradation of Chlorinated Solvents: Reactions near DNAPL and Enzyme Function

    SciTech Connect

    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

  13. Effects of oil pipeline explosion on ambient particulate matter and their associated polycyclic aromatic hydrocarbons.

    PubMed

    Zhao, Yue; Cao, Lixin; Zhou, Qing; Que, Qiming

    2015-01-01

    Effects of the oil pipeline explosion on PM(2.5)-associated polycyclic aromatic hydrocarbons (PAHs) and their substituted (alkylated, nitrated, oxygenated, hydroxyl and chlorinated) derivatives are assessed near the accident scene of Qingdao, China. Compared with those in TSP-PM(2.5), gaseous phase, burn residue and unburned crude oil, eighty-nine PAHs in PM(2.5) are identified and quantified to investigate the composition, temporal and spatial distribution, and sources. The concentrations of PM(2.5)-associated parent PAHs increase approximately seven times from the non-explosion samples to the explosion samples (mean ± standard deviation: 112 ± 2 vs 764 ± 15 ng/m(3)), while some substituted products (nitro- and oxy-) increase by two orders of magnitude (3117 ± 156 pg/m(3) vs 740 ± 37 ng/m(3)). The toxicity evaluation indicates the BaP equivalent concentrations (based on the US EPA's toxicity factors) in PM(2.5) are much higher than those in the other phases, especially for a long duration after the tragic accident.

  14. Ecological risk assessment of pesticide residues in coastal lagoons of Nicaragua.

    PubMed

    Carvalho, Fernando P; Villeneuve, Jean-Pierre; Cattini, Chantal; Tolosa, Immaculada; Montenegro-Guillén, S; Lacayo, Martha; Cruz, Adela

    2002-10-01

    A detailed investigation on the contamination with chlorinated hydrocarbons and organophosphorous pesticides of the coastal lagoon system of Chinandega district, Nicaragua, allowed the identification of contaminant sources and lagoon areas currently more contaminated. The discharge of rivers into the lagoons is the main transport pathway of pesticide residues; whereas atmospheric depositions are likely to be the main pathway for the introduction of PCBs into the lagoons. Analysis of water samples indicates widespread contamination with soluble organophosphorous compounds, such as dichlorvos, up to 410 ng L(-1), diazinon, up to 150 ng L(-1), and chlorpyrifos, up to 83 ng L(-1). Analyses of suspended matter for low solubility organochlorine (OC) compounds revealed very high concentrations of toxaphene, up to 17,450 ng g(-1) dry weight (dw), total DDTs up to 478 ng g(-1), Aroclor 1254, up to 119 ng g(-1) (dw), and lower concentrations for other compounds. Lagoon sediments contain high concentrations also of toxaphene, from 7.9 to 6,900 ng g(-1) (dw), and DDTs, from 1.5 to 321 ng g(-1) (dw), and lower concentrations of chlorpyrifos, hexachlorocyclohexanes, chlordane and other residues. Concentrations of OCs in soft tissues of clams are statistically correlated with the concentrations of the same compounds in bottom sediments, indicating that sediments are a source of contaminants to biota. In some areas of the lagoon system, concentration of residues in sediments are far above recommended threshold guideline values for protection of aquatic life, and may cause acute and chronic toxic effects on more sensitive aquatic species. Despite the ban on the use of toxaphene and DDT, residues of these compounds are still entering the lagoons due to erosion of, and leaching from, agriculture soils in the region. Measures for protection of the lagoon ecosystem are discussed.

  15. Chlorinated contaminants in chorio-allantoic membranes from great blue heron eggs at Whidbey Island Naval Air Station.

    PubMed

    Cobb, G P; Norman, D M; Miller, M W; Brewer, L W; Johnston, R K

    1995-01-01

    Chorio-allantoic membranes (CAMs) were collected and analyzed for chlorinated hydrocarbons as part of a wildlife toxicology demonstration project at Naval Air Station (NAS) Whidbey Island, Washington, USA. Concentrations of DDT, DDE, DDD, Aroclor 1254, and Aroclor 1260 were found at concentrations below 0.4 ppm for 13 of 14 samples. The low correlations among DDT and its metabolites in CAMs suggest herons are not being exposed to a consistent source of these compounds. Comparison of chlorinated hydrocarbon data for CAMs from three Puget Sound heron colonies, NAS Whidbey, Samish Island and Dumas Bay, indicates contaminant burdens in herons from NAS Whidbey and Samish Island are significantly lower than burdens in herons from Dumas Bay.

  16. Chlorine-induced cardiopulmonary injury.

    PubMed

    Carlisle, Matthew; Lam, Adam; Svendsen, Erik R; Aggarwal, Saurabh; Matalon, Sadis

    2016-06-01

    Chlorine (Cl2 ) is utilized worldwide for a diverse range of industrial applications, including pulp bleaching, sanitation, and pharmaceutical development. Though Cl2 has widespread use, little is known regarding the mechanisms of toxicity associated with Cl2 exposure, which occurs during industrial accidents or acts of terrorism. Previous instances of Cl2 exposure have led to reported episodes of respiratory distress that result in high morbidity and mortality. Furthermore, studies suggest that acute Cl2 exposure also results in systemic vascular injury and subsequent myocardial contractile dysfunction. Here, we review both lung and cardiac pathology associated with acute Cl2 inhalation and discuss recently published data that suggest that mitochondrial dysfunction underlies the pathogenesis of Cl2 -induced toxicity. Last, we discuss our findings that suggest that upregulation of autophagy protects against Cl2 -induced lung inflammation and can be a potential therapeutic target for ameliorating the toxic effects of Cl2 exposure. PMID:27303906

  17. The occurrence of chlorine in serpentine minerals

    USGS Publications Warehouse

    Miura, Y.; Rucklidge, J.; Nord, G.L.

    1981-01-01

    Partially serpentinized dunites containing small amounts of Chlorine (< 0.5%) from Dumont, Quebec, and Horoman, Hokkaido, Japan, and one containing less than 0.05% Chlorine from Higashi-Akaishi-Yama, Ehime, Japan have been examined using the electron probe microanalyzer and scanning transmission electron microscope with X-ray analytical capabilities. Chlorine was found together with Si, Mg, Ca and Fe in the serpentine minerals of the Dumont and Hokkaido dunites but not in the Ehime dunite. Chlorine is found associated only with the most finely crystalline facies of the serpentine (grain size less than 10 nm). The Ehime dunite contained no such fine grained serpentine, and was thus effectively chlorine-free, as are the coarser grained serpentines of the other samples. The finegrained chlorine-bearing serpentine also has a much higher concentration of Fe, and can contain smaller amounts of Ca, Ni and Mn than the coarse-grained variety as well as minute awaruite (FeNi3) grains. This fine-grained serpentine probably represents an early stage in the transformation of olivine to serpentine, with chlorine from hydrothermal solutions assisting the necessary chemical changes. The Cl increases the reaction rate by lowering the activation barrier to reaction by the introduction of reaction steps. ?? 1981 Springer-Verlag.

  18. Specific Sequence Motifs Direct the Oxygenation and Chlorination of Tryptophan by Myeloperoxidase

    PubMed Central

    Fu, Xiaoyun; Wang, Yi; Kao, Jeffery; Irwin, Angela; d’Avignon, André; Mecham, Robert P.; Parks, William C.; Heinecke, Jay W.

    2008-01-01

    Most studies of protein oxidation have typically focused on the reactivity of single amino acid side chains while ignoring the potential importance of adjacent sequences in directing the reaction pathway. We previously showed that hypochlorous acid (HOCl), a specific product of myeloperoxidase, inactivates matrilysin by modifying adjacent tryptophan and glycine (WG) residues in the catalytic domain. Here, we use model peptides that mimic the region of matrilysin involved in this reaction, VVWGTA, VVWATA and the library VVWXTA, to determine whether specific sequence motifs are targeted for chlorination or oxygenation by myeloperoxidase. Our results demonstrate that HOCl generated by myeloperoxidase or activated neutrophils converts the peptide VVWGTA to a chlorinated product, WG+32(Cl). Tandem mass spectrometry in concert with high resolution 1H and two-dimensional NMR analysis revealed that the modification required cross-linking of the tryptophan to the amide of glycine followed by chlorination of the indole ring of tryptophan. In contrast, when glycine in the peptide was replaced with alanine, the major products were mono- and di-oxygenated tryptophan residues. When the peptide library VVWXTA (where X represents all 20 common amino acids) was exposed to HOCl, only WG produced a high yield of the chloroindolenine derivative. However, when glycine was replaced by other amino acids, oxygenated tryptophan derivatives were the major products. Our observations indicate that WG may represent a specific sequence motif in proteins that is targeted for chlorination by myeloperoxidase. PMID:16548523

  19. Evaluation of short-term exposure to heated water and chlorine for control of the Asiatic clam (Corbicula fluminea)

    SciTech Connect

    Mattice, J.S.; McLean, R.B.; Burch, M.B.

    1982-01-01

    Based on the need for development of efficient procedures for prevention or control of fouling by the Asiatic clam, Corbicula fluminea, the response of these clams to chlorine in combination with rapid increases in water temperature was examined. Small clams were acclimated to 10 and 25/sup 0/C, and large clams were acclimated to 25/sup 0/C. Experiments with each of these acclimation groups consisted of variables of total residual chlorine concentration (0, 5, 7.5, and 10 mg/L) and test temperature (ambient and 3 test temperatures ranging from 35 to 46/sup 0/C). The periods of exposure to increased temperature and chlorine were 40 and 30 min respectively. Clam mortalities were related to water temperature but not to chlorine exposure. At high temperatures at least 50% of the clams remained open through the entire chlorine exposure period. At higher temperatures all of the clams remained open. Even when clams remained open for the entire 30-min chlorine exposure period, all clams were not killed. However, virtually all clams exposed to 41 to 43/sup 0/C water temperatures were killed whether open or closed during the exposure period. Death due to temperature shock is the logical conclusion from these data. Combined application of heated water and chlorine at the concentrations used is not more effective in killing Corbicula than is heated water alone. Current regulations on the concentration of chlorine in power plant effluents indicate that further studies of control of Corbicula using chlorine offer little likelihood for success. (ERB)

  20. Chlorine emissions from a medical waste incinerator.

    PubMed

    Murnyak, G R; Guzewich, D C

    1982-01-01

    Chloride/chlorine emissions from a hospital's medical waste incinerator were quantified in conjunction with a particulate emission stack test. Chlorine emissions averaged 100.5 mg/m3 with a standard deviation of 72 mg/m3 for five sample runs. It was estimated that the plastic content of the waste burned varied up to about 30%. Since, in general, emission standards for chlorine from medical waste incinerators do not exist, a simple diffusion model technique is suggested to estimate a safe distance to locate a medical waste incinerator from occupied buildings.

  1. Chlorination. Training Module 2.300.2.77.

    ERIC Educational Resources Information Center

    Kirkwood Community Coll., Cedar Rapids, IA.

    This document is an instructional module package prepared in objective form for use by an instructor familiar with chlorine, the reasons for chlorination and safe operation and maintenance of gas chlorine, dry calcium hypochlorite and liquid sodium hypochlorite chlorination systems for water supply and wastewater treatment facilities. Included are…

  2. Chlorination of Wastewater, Manual of Practice No. 4.

    ERIC Educational Resources Information Center

    Water Pollution Control Federation, Washington, DC.

    This manual reviews chlorination practices in the treatment and disposal of wastes from the earliest known applications. The application of chlorination for various purposes is described but no attempt has been made to compare chlorination with other methods. Included are chapters on the development and practice of wastewater chlorination,…

  3. Influence of Chlorine Emissions on Ozone Levels in the Troposphere

    EPA Science Inventory

    Chlorine emissions from cooling towers are emitted mainly as hypochlous acid, not as molecular chlorine. Chlorine emissions from cooling towers in electric utilities in the U.S. are estimated to be 4,400 tons per year. Molecular chlorine increases more tropospheric ozone than hyp...

  4. DETECTION OF CHLORINE DECAY PATTERNS IN WATER DISTRIBUTION DEAD-END FLOW REGIME UNDER VARIOUS HYDRODYNAMIC CONDITIONS

    EPA Science Inventory

    To further understand residual chlorine decay, a pilot-scale pipe dead-end zone was designed and fabricated at the U.S. EPA Test & Evaluation (T&E) facility in Cincinnati, Ohio. Preliminary studies have been conducted to characterize the hydrodynamic characteristics of the pilot...

  5. Hydrocarbon Spectral Database

    National Institute of Standards and Technology Data Gateway

    SRD 115 Hydrocarbon Spectral Database (Web, free access)   All of the rotational spectral lines observed and reported in the open literature for 91 hydrocarbon molecules have been tabulated. The isotopic molecular species, assigned quantum numbers, observed frequency, estimated measurement uncertainty and reference are given for each transition reported.

  6. Transfer of chlorine from the environment to agricultural foodstuffs.

    PubMed

    Kashparov, V; Colle, C; Levchuk, S; Yoschenko, V; Svydynuk, N

    2007-01-01

    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. PMID:17289228

  7. Behavior of chlorine during coal pyrolysis

    USGS Publications Warehouse

    Shao, D.; Hutchinson, E.J.; Cao, H.; Pan, W.-P.; Chou, C.-L.

    1994-01-01

    The behavior of chlorine in Illinois coals during pyrolysis was evaluated by combined thermo-gravimetry-Fourier transform infrared spectroscopy-ion chromatography (TG-FTIR-IC) techniques. It was found that more than 90% of chlorine in Illinois coals (IBC-103, 105, 106, and 109) was liberated as HCl gas during pyrolysis from 300 to 600??C, with the rate reaching a maximum at 440 ??C. Similarity of the HCl and NH3 release profiles during pyrolysis of IBC-109 supports the hypothesis that the chlorine in coal may be associated with nitrogen and the chlorine is probably bonded to the basic nitrogen sites on the inner walls of coal micropores. ?? 1994 American Chemical Society.

  8. Chlorine Salts at the Phoenix Landing Site

    NASA Astrophysics Data System (ADS)

    Hanley, J.; Horgan, B.

    2016-09-01

    Although chlorine salts (perchlorates, chlorides) are known to exist at the Phoenix landing site, their distribution and type have not been positively identified yet. We look for these salts through a novel NIR remote sensing technique.

  9. Ozone depletion and chlorine loading potentials

    NASA Technical Reports Server (NTRS)

    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.

  10. Innovative Technologies for Chlorinated Solvent Remediation

    NASA Astrophysics Data System (ADS)

    Pennell, Kurt D.; Cápiro, Natalie L.

    2014-07-01

    The following sections are included: * INTRODUCTION * TRADITIONAL REMEDIATION TECHNOLOGIES (1980s) * RESEARCH AND DEVELOPMENT OF INNOVATIVE REMEDIATION TECHNOLOGIES (1990s-2000s) * CURRENT TRENDS IN CHLORINATED SOLVENT REMEDIATION (2010s) * CLOSING THOUGHTS * REFERENCES

  11. Imidazole catalyzes chlorination by unreactive primary chloramines.

    PubMed

    Roemeling, Margo D; Williams, Jared; Beckman, Joseph S; Hurst, James K

    2015-05-01

    Hypochlorous acid and simple chloramines (RNHCl) are stable biologically derived chlorinating agents. In general, the chlorination potential of HOCl is much greater than that of RNHCl, allowing it to oxidize or chlorinate a much wider variety of reaction partners. However, in this study we demonstrate by kinetic analysis that the reactivity of RNHCl can be dramatically promoted by imidazole and histidyl model compounds via intermediary formation of the corresponding imidazole chloramines. Two biologically relevant reactions were investigated--loss of imidazole-catalyzed chlorinating capacity and phenolic ring chlorination using fluorescein and the tyrosine analog, 4-hydroxyphenylacetic acid (HPA). HOCl reacted stoichiometrically with imidazole, N-acetylhistidine (NAH), or imidazoleacetic acid to generate the corresponding imidazole chloramines which subsequently decomposed. Chloramine (NH2Cl) also underwent a markedly accelerated loss in chlorinating capacity when NAH was present, although in this case N-α-acetylhistidine chloramine (NAHCl) did not accumulate, indicating that the catalytic intermediate must be highly reactive. Mixing HOCl with 1-methylimidazole (MeIm) led to very rapid loss in chlorinating capacity via formation of a highly reactive chlorinium ion (MeImCl(+)) intermediate; this behavior suggests that the reactive forms of the analogous imidazole chloramines are their conjugate acids, e.g., the imidazolechlorinium ion (HImCl(+)). HOCl-generated imidazole chloramine (ImCl) reacted rapidly with fluorescein in a specific acid-catalyzed second-order reaction to give 3'-monochloro and 3',5'-dichloro products. Equilibrium constants for the transchlorination reactions HOCl + HIm = H2O + ImCl and NH2Cl + HIm = NH3 + ImCl were estimated from the dependence of the rate constants on [HIm]/[HOCl] and literature data. Acid catalysis again suggests that the actual chlorinating agent is HImCl(+); consistent with this interpretation, MeIm markedly catalyzed

  12. Imidazole catalyzes chlorination by unreactive primary chloramines

    PubMed Central

    Roemeling, Margo D.; Williams, Jared; Beckman, Joseph S.; Hurst, James K.

    2015-01-01

    Hypochlorous acid and simple chloramines (RNHCl) are stable biologically-derived chlorinating agents. In general, the chlorination potential of HOCl is much greater than that of RNHCl, allowing it to oxidize or chlorinate a much wider variety of reaction partners. However, in this study we demonstrate by kinetic analysis that the reactivity of RNHCl can be dramatically promoted by imidazole and histidyl model compounds via intermediary formation of the corresponding imidazole chloramines. Two biologically relevant reactions were investigated—loss of imidazole-catalyzed chlorinating capacity and phenolic ring chlorination using fluorescein and the tyrosine analog, 4-hydroxyphenylacetic acid (HPA). HOCl reacted stoichiometrically with imidazole, N-acetylhistidine (NAH), or imidazoleacetic acid to generate the corresponding imidazole chloramines which subsequently decomposed. Chloramine (NH2Cl) also underwent a markedly accelerated loss in chlorinating capacity when NAH was present, although in this case NAHCl did not accumulate, indicating that the catalytic intermediate must be highly reactive. Mixing HOCl with 1-methylimidazole (MeIm) led to very rapid loss in chlorinating capacity via formation of a highly reactive chlorinium ion (MeImCl+) intermediate; this behavior suggests that the reactive forms of the analogous imidazole chloramines are their conjugate acids, e.g., the imidazolechlorinium ion (HImCl+). HOCl-generated imidazole chloramine (ImCl) reacted rapidly with fluorescein in a specific acid-catalyzed second order reaction to give 3′-monochloro and 3′,5′-dichloro products. Equilibrium constants for the transchlorination reactions: HOCl + HIm = H2O + ImCl and NH2Cl + HIm = NH3 + ImCl were estimated from the dependence of the rate constants upon [HIm]/[HOCl] and literature data. Acid catalysis again suggests that the actual chlorinating agent is HImCl+; consistent with this interpretation, MeIm markedly catalyzed fluorescein chlorination by HOCl

  13. Comparative chlorine and temperature tolerance of the oyster Crassostrea madrasensis: implications for cooling system fouling.

    PubMed

    Rajagopal, S; Venugopalan, V P; van der Velde, G; Jenner, H A

    2003-04-01

    Crassostrea madrasensis is an important fouling oyster in tropical industrial cooling water systems. C. madrasensis individuals attach to surfaces by cementing one of their two valves to the substratum. Therefore, oyster fouling creates more problems than mussel fouling in the cooling conduits of power stations, because unlike the latter, the shell of the former remains attached to the substratum even after the death of the animal. However, there are no published reports on the tolerance of this species to chlorination and heat treatment. The mortality pattern and physiological behaviour (oxygen consumption and filtration rate) of three size groups (13 mm, 44 mm and 64 mm mean shell length) of C. madrasensis were studied at different residual chlorine concentrations (0.25, 0.5, 0.75, 1, 2, 3 to 5 mg 1-1) and temperatures (30 degrees C to 45 degrees C). The effect of shell size (= age) on C. madrasensis mortality in the presence of chlorine and taking into account temperature was significant, with the largest size group oysters showing highest resistance. At 1 mg l-1 residual chlorine, the 13 mm and 64 mm size group oysters, took 504 h (21 d) and 744 h (31 d), respectively to reach 100% mortality. At 39 degrees C, the 13 mm size group oysters took 218 min to reach 100% mortality, whereas the 64 mm size group oysters took 325 min. The oxygen consumption and filtration rate of C. madrasensis showed progressive reduction with increasing residual chlorine concentrations. However, the filtration rate and oxygen consumption responses of C. madrasensis were not significantly different between 30 degrees C (control) and 37.5 degrees C. There was a sharp decrease in the filtration rate and oxygen consumption at 38.5 degrees C. A comparison of the present mortality data with previous reports on other bivalves suggests that the chlorine tolerance of C. madrasensis lies in between that of Perna viridis and Perna perna, while its temperature tolerance is significantly higher

  14. Stratospheric chlorine: Blaming it on nature

    SciTech Connect

    Taube, G.

    1993-06-11

    Much of the bitter public debate over ozone depletion has centered on the claim that chlorofluorocarbons (CFCs) pale into insignificance alongside natural sources of chlorine in the stratosphere. If so, goes the argument, chlorine could not be depleting ozone as atmospheric scientists claim, because the natural sources have been around since time immemorial, and the ozone layer is still there. The claim, put forward in a book by Rogelio Maduro and Ralf Schauerhammer, has since been touted by former Atomic Energy Commissioner Dixy Lee Ray and talk-show host Rush Limbaugh, and it forms the basis of much of the backlash now being felt by atmospheric scientists. The argument is simple: Maduro and Schauerhammer calculate that 600 million tons of chlorine enters the atmosphere annually from seawater, 36 million tons from volcanoes, 8.4 million tons from biomass burning, and 5 million tons from ocean biota. In contrast, CFCs account for a mere 750,000 tons of atmospheric chlorine a year. Besides disputing the numbers, scientists have both theoretical and observational bases for doubting that much of this chlorine is getting into the stratosphere, where it could affect the ozone layer. Linwood Callis of the National Aeronautics and Space Administration's (NASA) Langley Research Center points out one crucial problem with the argument: Chlorine from natural sources is soluble, and so it gets rained out of the lower atmosphere. CFCs, in contrast, are insoluble and inert and thus make it to the stratosphere to release their chlorine. What's more, observations of stratospheric chemistry don't support the idea that natural sources are contributing much to the chlorine there.

  15. Photochemical Chlorine Activation From Artificial Saline Snowpacks

    NASA Astrophysics Data System (ADS)

    Wren, S. N.; Abbatt, J.; Donaldson, J.

    2012-12-01

    Halogen activation on snow and ice substrates has a profound influence on the oxidative capacity of the polar boundary layer. The release of reactive chlorine species is of particular interest since chlorine atoms can participate in both ozone depletion and organic oxidation. However, the mechanisms by which halides in sea ice substrates are converted into reactive halogen species are not well understood. In this study we investigated the photochemical activation of chlorine from artificial saline snow. Gas phase Cl2, BrCl and Br2 were detected using a chemical ionization mass spectrometer. We observe the dark release of Br2 in the presence of ozone; BrCl and Cl2 are only observed in the presence of both ozone and light. Interestingly, the release of reactive chlorine species persists when a 320 nm or a 380 nm long-pass filter is placed in the light path. Results suggest that smaller snow grains, which present a larger total snow surface area, enhance chlorine production to a greater extent than BrCl or Br2 production. Here we also present the effect of temperature (above and below the NaCl euctectic), acidity, chloride concentration, and ozone concentration on the production of Br2, BrCl and Cl2. Overall the results indicate that a mechanism involving UV-A light and ozone leads to chlorine activation, which may be particularly important in bromide-depleted snow.

  16. Chemistry of saline-water chlorination

    SciTech Connect

    Haag, W.R.

    1981-06-01

    Vast quantities of natural waters are used by power plants for cooling purposes. This water is chlorinated to prevent slime build-up inside the cooling pipes, is circulated through the cooling system, and eventually discharged back into the water body. In order to assess the environmental impact of water chlorination, it is necessary to know what chemical compounds are produced and discharged into the receiving waters. To attack this problem, a review of the present state of knowledge of natural water chlorination chemistry was performed, and some experimental work explained the results of previous workers by showing that chlorine losses at very high doses in seawater are simply the result of chlorate and bromate formation which, however, is negligible at normal doses. The most important chlorine-produced oxidants, along with the relevant chemical reactions, were chosen as a basis for a kinetic model of saline water chlorination chemistry. Kinetic data were compiled in a computer program which simultaneously solves 24 differential equations, one for each species modelled. Estimates were made for the unknown rate constants. A purely predictive model was not possible due to the great variability in the organic demand; however, the model is applicable under a broad variety of conditions (except sunlight), and it provides a reasonably good description of a halamine chemistry under environmental conditions.

  17. Using Water To Analyze Greasy Residues

    NASA Technical Reports Server (NTRS)

    Hoppesch, Charles W.

    1994-01-01

    Water found useful as substitute for chlorofluorocarbon (CFC) solvents in tests to measure amounts of nonvolatile residues of contaminants (e.g., hydrocarbon greases) on equipment after it has been cleaned. Water does not harm environment and much cheaper than CFCs.

  18. Maxillofacial prostheses of chlorinated polyethylene.

    PubMed

    May, P D

    1978-05-01

    There is clearly a need for maxillofacial prosthetic materials with improved properties. The chlorinated polyethylenes are thermoplastic elastomers which have particularly promising properties, and were used by us to prepare improved maxillofacial prostheses. Suitable CPE resins were compounded with other polymers and with pigments on a heated rubber mill to form thin sheets in a variety of shades. These were heated at 190 degrees C for 10 min and placed between heated linotype mold halves. The prosthesis was formed in a hand press. Sometimes heating and pressing were repeated. After cooling in water, the prosthesis was removed and hand-shaded with oil-soluble dyes. Physical properties were evaluated using standard techniques; skin irritation studies were conducted by 14-day insult patch tests on rabbits. Clinical evaluations were conducted on human volunteers. Parallel evaluations were conducted on commerically available materials for comparison. The CPE was superior to all of the three commerical materials in most properties, and comparable to the better of the three in the remaining properties. On balance, CPE was significantly superior. Early results indicate that the materials and techniques required are easily handled in the dental lab and that the final prosthesis has excellent aesthetic and patient acceptability. PMID:670262

  19. Chlorine isotope composition of volcanic gases and rocks at Mount Etna (Italy) and inferences on the local mantle source

    NASA Astrophysics Data System (ADS)

    Rizzo, Andrea L.; Caracausi, Antonio; Liotta, Marcello; Paonita, Antonio; Barnes, Jaime D.; Corsaro, Rosa A.; Martelli, Mauro

    2013-06-01

    We present the first chlorine isotope compositional data for gases and lavas from Mount Etna (Italy), and to our knowledge, of active Mediterranean volcanism. We investigated lavas erupted and gases discharged during 2008-2011 from a high-temperature fumarole (HT; >300 °C) and plume gases from both North East and Central Craters. Most of the samples vary in a narrow range of chlorine isotope composition (δ37Cl values≈0±0.7‰) with gases partially overlapping with rocks. Only HT gases sampled in 2009 have been clearly affected by secondary processes (δ37Cl values>15.9‰), resulting in partial removal of chlorine and isotopic fractionation producing a 37Cl enrichment in the residual gaseous HCl. These secondary processes also affect, although to a lesser extent, plume gases from North East Crater (NEC). Although post-magmatic processes are able to modify the chlorine isotope composition, δ37Cl values are not affected by magma degassing for residual fractions ≥0.3 in the melt, or any effect is within our data variability. Finally, δ37Cl values and Cl/K ratios of magmatic chlorine constrain the Etnean source to be compatible with depleted mantle (DMM) contaminated by altered oceanic crust (AOC), in agreement with indications from more common isotopic tracers of mantle processes.

  20. Plasma Processing Of Hydrocarbon

    SciTech Connect

    Grandy, Jon D; Peter C. Kong; Brent A. Detering; Larry D. Zuck

    2007-05-01

    The Idaho National Laboratory (INL) developed several patented plasma technologies for hydrocarbon processing. The INL patents include nonthermal and thermal plasma technologies for direct natural gas to liquid conversion, upgrading low value heavy oil to synthetic light crude, and to convert refinery bottom heavy streams directly to transportation fuel products. Proof of concepts has been demonstrated with bench scale plasma processes and systems to convert heavy and light hydrocarbons to higher market value products. This paper provides an overview of three selected INL patented plasma technologies for hydrocarbon conversion or upgrade.

  1. Rapeseed lecithin hydroxylation by chlorine replacing with hydroxyl groups in chlorinated phospholipids.

    PubMed

    Górecki, Michał; Sosada, Marian; Boryczka, Monika; Fraś, Pawel; Pasker, Beata

    2012-01-01

    Rapeseed lecithin ethanol soluble fraction (LESF) was hydroxylated with 30% hydrogen peroxide in the presence of acetic acid. The product was compared to the one obtained by method based on nucleophilic substitution reaction of phospholipids chlorine derivatives. In this approach, hydrogen chloride was added to double bonds in unsaturated acyl groups of phospholipids. Next, chlorine was replaced with hydroxyl groups via the alkaline hydrolysis of chlorine derivatives. The surface active properties of the products obtained with the usage of two methods of rapeseed LESF hydroxylation were determined. The minimal surface tension (eta(min), mN/m) and the critical micelle concentration (CMC, g/L) of LESF hydroxylated with hydrogen peroxide (20.2 mN/m, 6.0 g/L) and obtained by chlorine replacing with hydroxyl groups in chlorinated phospholipids (25.0 mN/m, 9.8 g/L) were compared to LESF (31.8 mN/m, 17.8 g/L). Hydroxylated LESF obtained by lecithin chlorination and chlorine replacing with hydroxyl groups in the chlorine derivatives has no peroxides and the good surface active properties. The product as an effective emulsifier can be used in pharmacy and cosmetics.

  2. Effects of chlorine and chlorine dioxide on human rotavirus infectivity and genome stability.

    PubMed

    Xue, Bin; Jin, Min; Yang, Dong; Guo, Xuan; Chen, Zhaoli; Shen, Zhiqiang; Wang, Xinwei; Qiu, Zhigang; Wang, Jingfeng; Zhang, Bin; Li, Junwen

    2013-06-15

    Despite the health risks posed by waterborne human rotavirus (HRV), little information is available concerning the effectiveness of chlorine or chlorine dioxide (ClO2), two common disinfectants of public water sources, against HRV and their effects on its genome remain poorly understood. This study investigated the effects of chlorine and ClO2 on purified HRV by using cell culture and RT-PCR to assess virus infectivity and genetic integrity, respectively. The disinfection efficacy of ClO2 was found to be higher than that of chlorine. According to the efficiency factor Hom model, Ct value (mg/L min) ranges required for a 4-log reduction of HRV at 20 °C by chlorine and ClO2 were 5.55-5.59 and 1.21-2.47 mg/L min, respectively. Detection of the 11 HRV genome segments revealed that damage to the 1227-2354 bp of the VP4 gene was associated with the disappearance of viral infectivity by chlorine. However, no complete accordance between culturing and RT-PCR assays was observed after treatment of HRV with ClO2. These results collectively indicate that the current practice of chlorine disinfection may be inadequate to manage the risk of waterborne HRV infection, and offer the potential to monitor the infectivity of HRV adapting PCR-based protocols in chlorine disinfection.

  3. Effect of UV irradiation on the proportion of organic chloramines in total chlorine in subsequent chlorination.

    PubMed

    Zhang, Tian-Yang; Lin, Yi-Li; Xu, Bin; Xia, Sheng-Ji; Tian, Fu-Xiang; Gao, Nai-Yun

    2016-02-01

    This study investigated the changes of chlorine species and proportion of organic chloramines during the chlorination process after UV irradiation pretreatment in drinking water. It was found that the UV pretreatment could enhance the percentage of organic chloramines by increasing free chlorine consumption in the chlorination of raw waters. The percentage of organic chloramines in total chlorine increased with UV intensity and irradiation time in raw waters. However, for the humic acid synthesized water, the percentage of organic chloramines increased first and then decreased with the increase of UV irradiation time. The value of SUVA declined in both raw and humic acid synthesized waters over the UV irradiation time, which indicated that the decomposition of aromatic organic matter by UV could be a contributor to the increase of free chlorine consumption and organic chloramine proportion. The percentage of organic chloramines during chlorination of raw waters after 30-min UV irradiation pretreatment varied from 20.2% to 41.8%. Total chlorine decreased obviously with the increase of nitrate concentration, but the percentage of organic chloramines increased and was linearly correlated to nitrate concentration.

  4. Solvent dewaxing waxy hydrocarbon oils using dewaxing aid

    SciTech Connect

    Komine, K.; Naito, T.; Ohashi, F.; Onodera, T.

    1982-02-16

    In a solvent dewaxing process wherein a waxy hydrocarbon oil is mixed with a dewaxing aid and dewaxing solvent and chilled to form a slurry comprising solid particles of wax and a mixture of dewaxed oil and solvent, the improvement which comprises using a polymeric dewaxing aid comprising a condensation product of naphthalene and chlorinated wax having an average molecular weight ranging from about 20,000 to 500,000 and a molecular weight distribution exceeding the range of from about 10,000 to 1 ,000,000.

  5. Chlorination and water quality monitoring within a public drinking water supply in Rawalpindi Cantt (Westridge and Tench) area, Pakistan.

    PubMed

    Hashmi, Imran; Farooq, Shaukat; Qaiser, Sara

    2009-11-01

    Concern over the presence of fecal coliform in public drinking water supplies has been expressed in recent years in Pakistan since it has been regarded as pathogenic organism of prime importance in gastroenteritis. Two major drinking water distribution systems in the Cantt area of Rawalpindi district covering the Westridge and Tench areas was monitored over a 2-month period to determine the prevalence of fecal coliform and chlorine residual. The collected samples were examined for total chlorine, free chlorine residual, chloramines, total coliforms, fecal coliforms, and turbidity. The drinking water quality monitoring in the distribution network was performed by collecting samples from water source, overhead reservoir, and residential taps. In the Westridge area, total chlorine varied from the lowest value of 0.27 mg/L at Station # W-5 to the highest value of 0.42 mg/L at Station # W-2, total coliforms varied from 1.1 to 3.6 most probable number (MPN)/100 mL with presence of Escherichia coli in all samples, total dissolved solids (TDS) ranged from 199.5 to 205 mg/L, conductivity fluctuated between 399 and 411 microS/cm, and turbidity varied from 0.43 to 0.73 NTU. In the Tench area, the value of total chlorine ranged from 0.14 mg/L at Station # T-7 to 0.55 mg/L at Station # T-1. Total coliform varied from 3.6 to 5.1 MPN/100 mL and fecal coliform were detected at all the stations except at Station # T-1. TDS ranged from 201.4 to 257 mg/L, conductivity varied from 343 to 513 microS/cm, and turbidity ranged between 0.66 and 1.55 NTU. It is recommended to the respective agencies to ensure that the chlorine residual is available at consumer end.

  6. Kidney cancer and hydrocarbon exposures among petroleum refinery workers.

    PubMed Central

    Poole, C; Dreyer, N A; Satterfield, M H; Levin, L; Rothman, K J

    1993-01-01

    To evaluate the hypothesis of increased kidney cancer risk after exposure to hydrocarbons, especially those present in gasoline, we conducted a case-control study in a cohort of approximately 100,000 male refinery workers from five petroleum companies. A review of 18,323 death certificates identified 102 kidney cancer cases, to each of whom four controls were matched by refinery location and decade of birth. Work histories, containing an average of 15.7 job assignments per subject, were found for 98% of the cases and 94% of the controls. To each job, industrial hygienists assigned semiquantitative ratings for the intensity and frequency of exposures to three hydrocarbon categories: nonaromatic liquid gasoline distillates, aromatic hydrocarbons, and the more volatile hydrocarbons. Ratings of "present" or "absent" were assigned for seven additional exposures: higher boiling hydrocarbons, polynuclear aromatic hydrocarbons, asbestos, chlorinated solvents, ionizing radiation, and lead. Each exposure had either no association or a weak association with kidney cancer. For the hydrocarbon category of principal a priori interest, the nonaromatic liquid gasoline distillates, the estimated relative risk (RR) for any exposure above refinery background was 1.0 (95% confidence interval [CI] 0.5-1.9). Analyses of cumulative exposures and of exposures in varying time periods before kidney cancer occurrence also produced null or near-null results. In an analysis of the longest job held by each subject (average duration 9.2 years or 40% of the refinery work history), three groups appeared to be at increased risk: laborers (RR = 1.9, 95% CI 1.0-3.9); workers in receipt, storage, and movements (RR = 2.5, 95% CI 0.9-6.6); and unit cleaners (RR = 2.3, 95% CI 0.5-9.9). PMID:8020449

  7. Chlorine treatment effectiveness and physico-chemical and bacteriological characteristics of treated water supplies in distribution networks of Accra-Tema Metropolis, Ghana

    NASA Astrophysics Data System (ADS)

    Karikari, A. Y.; Ampofo, J. A.

    2013-06-01

    Drinking water quality from two major treatment plants in Ghana; Kpong and Weija Plants, and distribution networks in the Accra-Tema Metropolis were monitored monthly for a year at fifteen different locations. The study determined the relationship between chlorine residual, other physico-chemical qualities of the treated water, and, bacteria regrowth. Results indicated that the treated water at the Kpong and Weija Treatment Plants conformed to WHO guidelines for potable water. However, the water quality deteriorated bacteriologically, from the plants to the delivery points with high numbers of indicator and opportunistic pathogens. This could be due to inadequate disinfection residual, biofilms or accidental point source contamination by broken pipes, installation and repair works. The mean turbidity ranged from 1.6 to 2.4 NTU; pH varied from 6.8 to 7.4; conductivity fluctuated from 71.1 to 293 μS/cm. Chlorine residual ranged from 0.13 to 1.35 mg/l. High residual chlorine was observed at the treatment plants, which decreased further from the plants. Results showed that additional chlorination does not take place at the booster stations. Chlorine showed inverse relationship with microbial counts. Total coliform bacteria ranged from 0 to 248 cfu/100 ml, and faecal coliform values varied from 0 to 128 cfu/100 ml. Other microorganisms observed in the treated water included Aeromonas spp., Clostridium spp. and Pseudomonas spp. Boiling water in the household before consumption will reduce water-related health risks.

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

    PubMed

    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.

  9. Water chlorination: An enigma for modern-day environmental chemists

    SciTech Connect

    Johnson, J.D.; Jolley, R.L.

    1987-01-01

    The challenge of modern-day water chlorination is to reap the benefits of chlorine's excellent disinfection efficacy while minimizing its environmental impacts and byproduct toxicity. Chemists, biologists, and engineers need to work together to identify, quantify, and use most effectively the disinfectant forms of chlorine to maximize disinfection, while at the same time they also need to identify, quantify, and minimize the toxic forms of by-products produced by chlorine's reactions with the organic compounds found in water. To the extent that this is possible, we can enjoy the benefits of chlorine disinfection and minimize the human and environmental impacts of chlorination by-products. 22 refs.

  10. Modeling the accumulation of three waterborne chlorinated ethanes in fathead minnows (Pimephales promelas): A physiologically based approach

    SciTech Connect

    Lien, G.J.; Nichols, J.W.; McKim, J.M. . Environmental Research Lab.); Gallinat, C.A. )

    1994-07-01

    A physiologically based kinetic model was used to predict the accumulation of a homologous series of chlorinated ethanes in fathead minnows (Pimephales promelas). Uptake and accumulation of these compounds are described in terms of a few fundamental physiological, morphological, and physicochemical parameters. Chemical residues in 30-d-old fathead minnows exposed to 1,1,2,2-tetrachloroethane, pentachloroethane, and hexachloroethane were used to evaluate model performance. The predicted and observed accumulations of the chlorinated ethanes were in close agreement. A quantitative assessment of the major factors regulating the exchanged of these compounds indicates that the cutaneous surface may be an important route of uptake in small fish.

  11. Modeling the accumulation of three waterborne chlorinated ethanes in fathead minnows ( pimephales promelas'): A physiologically based approach

    SciTech Connect

    Lien, G.J.; Nichols, J.W.; McKim, J.M.; Gallinat, C.A.

    1994-01-01

    A physiologically based kinetic model was used to predict the accumulation of a homologous series of chlorinated ethanes in fathead minnows (Pimephales promelas). Uptake and accumulation of these compounds are described in terms of a few fundamental physiological, morphological, and physicochemical parameters. Chemical residues in 30-d-old fathead minnows exposed to 1,1,2,2-tetrachloroethane, pentachloroethane, and hexachloroethane were used to evaluate model performance. The predicted and observed accumulations of the chlorinated ethanes were in close agreement. A quantitative assessment of the major factors regulating the exchange of these compounds indicates that the cutaneous surface may be an important route of uptake in small fish.

  12. Membrane separation of hydrocarbons

    DOEpatents

    Funk, Edward W.; Kulkarni, Sudhir S.; Chang, Y. Alice

    1986-01-01

    Mixtures of heavy oils and light hydrocarbons may be separated by passing the mixture over a polymeric membrane which comprises a polymer capable of maintaining its integrity in the presence of hydrocarbon compounds at temperature ranging from about ambient to about 100.degree. C. and pressures ranging from about 50 to about 1000 psi. The membranes which possess pore sizes ranging from about 10 to about 500 Angstroms are cast from a solvent solution and recovered.

  13. Hydrocarbon geoscience research strategy

    SciTech Connect

    Not Available

    1990-04-01

    This document outlines a strategy for oil and gas related research focused on optimizing the economic producibility of the Nation's resources. The Hydrocarbon Geoscience Strategy was developed by the Hydrocarbon Geoscience Research Coordinating Committee of the Department of Energy (DOE). This strategy forms the basis for the development of DOE Fossil Energy's Oil Research Program Implementation Plan and Natural Gas Program Implementation Plan. 24 refs., 5 figs., 3 tabs.

  14. Chlorine truck attack consequences and mitigation.

    PubMed

    Barrett, Anthony Michael; Adams, Peter J

    2011-08-01

    We develop and apply an integrated modeling system to estimate fatalities from intentional release of 17 tons of chlorine from a tank truck in a generic urban area. A public response model specifies locations and actions of the populace. A chemical source term model predicts initial characteristics of the chlorine vapor and aerosol cloud. An atmospheric dispersion model predicts cloud spreading and movement. A building air exchange model simulates movement of chlorine from outdoors into buildings at each location. A dose-response model translates chlorine exposures into predicted fatalities. Important parameters outside defender control include wind speed, atmospheric stability class, amount of chlorine released, and dose-response model parameters. Without fast and effective defense response, with 2.5 m/sec wind and stability class F, we estimate approximately 4,000 (half within ∼10 minutes) to 30,000 fatalities (half within ∼20 minutes), depending on dose-response model. Although we assume 7% of the population was outdoors, they represent 60-90% of fatalities. Changing weather conditions result in approximately 50-90% lower total fatalities. Measures such as sheltering in place, evacuation, and use of security barriers and cryogenic storage can reduce fatalities, sometimes by 50% or more, depending on response speed and other factors. PMID:21395636

  15. Chlorination of organophosphorus pesticides in natural waters.

    PubMed

    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.

  16. Temporal Decrease in Upper Atmospheric Chlorine

    NASA Technical Reports Server (NTRS)

    Froidevaux, L.; Livesey, N. J.; Read, W. G.; Salawitch, R. J.; Waters, J. W.; Drouin, B.; MacKenzie, I. A.; Pumphrey, H. C.; Bernath, P.; Boone, C.; Nassar, R.; Montzka, S.; Elkins, J.; Cunnold, D.; Waugh, D.

    2006-01-01

    We report a steady decrease in the upper stratospheric and lower mesospheric abundances of hydrogen chloride (HCl) from August 2004 through January 2006, as measured by the Microwave Limb Sounder (MLS) aboard the Aura satellite. For 60(deg)S to 60(deg)N zonal means, the average yearly change in the 0.7 to 0.1 hPa (approx.50 to 65 km) region is -27 +/- 3 pptv/year, or -0.78 +/- 0.08 percent/year. This is consistent with surface abundance decrease rates (about 6 to 7 years earlier) in chlorine source gases. The MLS data confirm that international agreements to reduce global emissions of ozone-depleting industrial gases are leading to global decreases in the total gaseous chlorine burden. Tracking stratospheric HCl variations on a seasonal basis is now possible with MLS data. Inferred stratospheric total chlorine (CITOT) has a value of 3.60 ppbv at the beginning of 2006, with a (2-sigma) accuracy estimate of 7%; the stratospheric chlorine loading has decreased by about 43 pptv in the 18-month period studied here. We discuss the MLS HCl measurements in the context of other satellite-based HCl data, as well as expectations from surface chlorine data. A mean age of air of approx. 5.5 years and an age spectrum width of 2 years or less provide a fairly good fit to the ensemble of measurements.

  17. Chlorine truck attack consequences and mitigation.

    PubMed

    Barrett, Anthony Michael; Adams, Peter J

    2011-08-01

    We develop and apply an integrated modeling system to estimate fatalities from intentional release of 17 tons of chlorine from a tank truck in a generic urban area. A public response model specifies locations and actions of the populace. A chemical source term model predicts initial characteristics of the chlorine vapor and aerosol cloud. An atmospheric dispersion model predicts cloud spreading and movement. A building air exchange model simulates movement of chlorine from outdoors into buildings at each location. A dose-response model translates chlorine exposures into predicted fatalities. Important parameters outside defender control include wind speed, atmospheric stability class, amount of chlorine released, and dose-response model parameters. Without fast and effective defense response, with 2.5 m/sec wind and stability class F, we estimate approximately 4,000 (half within ∼10 minutes) to 30,000 fatalities (half within ∼20 minutes), depending on dose-response model. Although we assume 7% of the population was outdoors, they represent 60-90% of fatalities. Changing weather conditions result in approximately 50-90% lower total fatalities. Measures such as sheltering in place, evacuation, and use of security barriers and cryogenic storage can reduce fatalities, sometimes by 50% or more, depending on response speed and other factors.

  18. Accumulation of chlorinated benzenes in earthworms

    SciTech Connect

    Beyer, W.N.

    1996-12-31

    Chlorinated benzenes are widespread in the environment. Hexachlorobenzene, pentachlorobenzene and all isomers of dichlorobenzenes, trichlorobenzenes, and tetrachlorobenzenes, have been detected in fish, water, and sediments from the Great Lakes. They probably entered the water as leachates from chemical waste dumps and as effluents from manufacturing. Hexachlorobenzene and pentachlorobenzene are commonly present in Herring gull (Larus argentatus) eggs from the Great Lakes, and some of the isomers of trichlorobenzene and tetrachlorobenzene are occasionally detected at low concentrations. Hexachlorobenzene, which was formerly used as a fungicide, has been the most thoroughly studied chlorinated benzene, and has been detected in many species. Its use as a fungicide in the United States was canceled in 1984. Since about 1975 hexachlorobenzene has been formed mainly in the production of chlorinated solvents. It is highly persistent in the environment and some species are poisoned by hexachlorobenzene at very low chronic dietary exposures. As little as 1 ppm in the diet of mink (Mustela vison) reduced the birth weights of young, and 5 ppm in the diet of Japanese quail (Coturnix coturnix japonica) caused slight liver damage. This paper describes a long-term (26 wk) experiment relating the concentrations of chlorinated benzenes in earthworms to length of exposure and three 8 wk experiments relating concentration to the concentration in soil the soil organic matter content, and the degree of chlorination. 20 refs., 3 figs., 1 tab.

  19. Classification and modelling of non-extractable residue (NER) formation from xenobiotics in soil - a synthesis

    NASA Astrophysics Data System (ADS)

    Kaestner, Matthias; Nowak, Karolina; Miltner, Anja; Trapp, Stefan; Schaeffer, Andreas

    2014-05-01

    This presentation provides a comprehensive overview about the formation of non-extractable residues (NER) from organic pesticides and contaminants in soil and tries classifying the different types. Anthropogenic organic chemicals are deliberately (e.g. pesticides) or unintentionally (e.g. polyaromatic hydrocarbons [PAH], chlorinated solvents, pharmaceuticals) released in major amounts to nearly all compartments of the environment. Soils and sediments as complex matrices provide a wide variety of binding sites and are the major sinks for these compounds. Many of the xenobiotics entering soil undergo turnover processes and can be volatilised, leached to the groundwater, degraded by microorganisms or taken up and enriched by living organisms. Xenobiotic NER may be derived from parent compounds and primary metabolites that are sequestered (sorbed or entrapped) within the soil organic matter (type I NER) or can be covalently bound (type II NER). Especially type I NER may pose a considerably environmental risk of potential release. However, NER resulting from productive biodegradation, which means the conversion of carbon (or nitrogen) from the compounds into microbial biomass molecules during microbial degradation (type III, bioNER), do not pose any risk. Experimental and analytical approaches to clearly distinguish between the types are provided and a model to prospectively estimate their fate in soil is proposed.

  20. Formation of disinfection by-products in chlorinated swimming pool water.

    PubMed

    Kim, Hekap; Shim, Jaeho; Lee, Soohyung

    2002-01-01

    The formation of five volatile disinfection by-products (DBPs: chloroform, bromodichloromethane, chloral hydrate, dichloroacetonitrile, and 1,1,1-trichloropropanone) by the chlorination of the materials of human origin (MHOs: hair, lotion, saliva, skin, and urine) in a swimming pool model system was examined. Chlorination reactions took place with a sufficient supply of chlorine residuals (0.84 mg Cl2/l < total chlorine < 6.0 mg Cl2/l) in 300 ml glass bottles containing either ground water or surface water as a reaction medium at 30 degrees C and pH 7.0, for either 24 or 72 h. A longer reaction period of 72 h or a higher content of organic materials led to the increased formation of DBPs. Of the DBPs formed by the reaction, chloroform was a major compound found in both ground and surface waters. The formation of chloroform and bromodichloromethane per unit total organic carbon (TOC) concentration was suppressed when all types of MHOs were added to the surface water that already contained DBP precursors such as humic substances. However, the formation of dichloroacetonitrile was promoted, probably due to the increased degradation reactions of nitrogen-containing compounds such as urea and proteins of human origin. In conclusion, the materials of swimmers' origin including hair, lotion, saliva, skin, and urine add to the levels of DBPs in swimming pool water, and any mitigation measures such as periodic change of water are needed to protect swimmers from elevated exposures to these compounds.