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Sample records for evaluating chlorinated hydrocarbon

  1. Evaluation of Chlorinated Hydrocarbon Concentrations in Tehran’s Districts Drinking Water

    Directory of Open Access Journals (Sweden)

    Alireza Pardakhti

    2012-01-01

    Full Text Available In this study Tehran’s drinking water was evaluated for the presence of chlorinated hydrocarbons during spring and summer of 2009. Chlorinated hydrocarbons are an important class of environmental pollutants that cause adverse health effects on human’s kidney, liver and central nervous systems. In this study six water districts were selected for taking drinking water samples in the city of Tehran as well as one location outside the city limits. The samples were analyzed by GC/MS using EPA method 8260. The average concentrations of 1,1-dichloroethylene, 1,2 Dichloromethane, Tetra chloromethane, Trichloroethylene and tetra chloroethylene were determined during a 7 month period and the results were 0.04ppb, 0.52ppb, 0.01ppb, 0.24ppb, 0.03ppb respectively. The highest concentration of chlorinated hydrocarbon observed in Tehran’s drinking water was Trichloroethylene and the lowest concentration was Tetra chloromethane. Districts 5 and 6 showed the highest concentrations of chlorinated hydrocarbons in the city of Tehran.

  2. Push-Pull Tests for Evaluating the Aerobic Cometabolism of Chlorinated Aliphatic Hydrocarbons

    National Research Council Canada - National Science Library

    Semprini, Lew

    2006-01-01

    .... This report describes a newly developed single-well technology for evaluating the feasibility of using in situ aerobic cometabolic processes to treat groundwater contaminated with chlorinated solvent mixtures...

  3. Push-Pull Tests for Evaluating the Aerobic Cometabolism of Chlorinated Aliphatic Hydrocarbons: Cost & Performance Report

    National Research Council Canada - National Science Library

    Semprini, Lew

    2006-01-01

    .... This report describes a newly developed single-well technology for evaluating the feasibility of using in situ aerobic cometabolic processes to treat groundwater contaminated with chlorinated solvent mixtures...

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

    Energy Technology Data Exchange (ETDEWEB)

    Brigmon, R.L.; Franck, M.M.; Brey, J.; Fliermans, C.B. [Westinghouse Savannah River, Aiken, SC (United States). Environmental Biotechnology Section; Scott, D.; Lanclos, K. [Medical Coll. of Georgia, Augusta, GA (United States)

    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.

  5. Hydrochloric acid recycling from chlorinated hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

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

    1993-12-31

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

  6. Hydrochloric acid recycling from chlorinated hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

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

    1994-12-31

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

  7. Radiolytic degradation of chlorinated hydrocarbons in water

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Xing-Zheng; Yamamoto, Takeshi [Fukui Univ., Faculty of Engineering, Dept. of Materials Science and Engineering, Fukui (Japan); Hatashita, Masanori [The Wakasa Wan Energy Research Center, Research Dept., Tsuruga, Fukui (Japan)

    2002-11-01

    Radiolytic degradation of chlorinated hydrocarbons (chloroform, trichloroethylene, and tetrachloroethylene) in water was carried out. Water solutions of the chlorinated hydrocarbons with different concentrations were irradiated with {gamma} rays. Concentrations of methane, ethane, CO, CO{sub 2}, H{sub 2}, and O{sub 2} after the irradiation were determined by gas chromatography. Concentration of chloride ion in the irradiated sample was determined by ion chromatography. Experimental results show that radiolytic degradation of the chlorinated hydrocarbon increased with the radiation dose. Methane, ethane, CO{sub 2}, H{sub 2}, and Cl{sup -} concentrations increased with the radiation dose and the sample concentration. On the other hand, O{sub 2} concentration decreased with the radiation dose and the sample concentration. When sample concentration was high, dissolved oxygen might be not enough for converting most of the C atoms in the sample into CO{sub 2}. This resulted in a low decomposition ratio. Addition of H{sub 2}O{sub 2} as an oxygen resource could increase the decomposition ratio greatly. Furthermore, gas chromatography-mass spectroscopy was applied to identify some intermediates of the radiolytic dehalogenation. Radiolytic degradation mechanisms are also discussed. (author)

  8. Detecting chlorinated hydrocarbon residues: Rachel Carson's villains.

    Science.gov (United States)

    Travis, Anthony S

    2012-07-01

    In 1962, Rachel Carson's Silent Spring drew the public's attention to the deleterious effects of chlorinated hydrocarbons employed as economic poisons in agriculture. However, she did not discuss how their residues could be routinely identified and quantified. In part, this was because the introduction of instruments for use in environmental analysis had only just begun, and she was probably unaware of their existence. The development of the instrumental methods began in industry, particularly at Dow and Shell, in the mid-1950s. Dow scientists, by combining mass spectrometry with gas chromatography, developed the most powerful technique, then and now, for the separation, quantitation and identification of chlorinated hydrocarbons. Shell scientists were no less innovative, particularly with the application of highly sensitive gas chromatography detectors to trace analysis. The first of these detectors, the electron capture detector, was invented by James Lovelock at the National Institute of Medical Research, North London, at the end of the 1950s. Around the same time, Dale Coulson in the USA developed his microcoulometric detector.

  9. Chlorinated hydrocarbons in a pelagic community

    International Nuclear Information System (INIS)

    Elder, D.; Fowler, S.W.

    1976-01-01

    For several years data have been accruing on the distribution of chlorinated hydrocarbon pollutants in marine ecosystems. An overall picture of ambient levels in biota, water and sediments is now emerging however, despite the vast amount of data collected to date, questions still arise as to whether certain pollutants such as chlorinated hydrocarbons are indeed magnified through the marine food web. Evidence both for and against trophic concentration of PCB and DDT compounds has been cited. The answer to this question remains unclear due to lack of adequate knowledge on the relative importance of food and water in the uptake of these compounds as well as the fact that conclusions are often confounded by comparing pollutant concentrations in successive links in the food chain sampled at different geographical locations and/or at different points in time. The situation is further complicated by complex prey-predator relationships that exist in many marine communities. In the present study we have tried to eliminate some of these problems by examining PCB and DOT concentrations in species belonging to a relatively well-defined pelagic food chain sampled at one point in space and time

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

    NARCIS (Netherlands)

    Atashgahi, S.; Maphosa, F.; Vrieze, de J.; Haest, P.J.; Boon, N.; Smidt, H.; Springael, D.; Dejonghe, W.

    2014-01-01

    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

  11. Evaluation of anaerobic in-situ bioremediation of chlorinated hydrocarbons and BTEX with laboratory microcosm and PCR

    Energy Technology Data Exchange (ETDEWEB)

    Gemoets, J.; Lookman, R.; Borremans, B.; Ceuster, T. de [VITO, Mol (Belgium)

    2003-07-01

    The results of a number of microcosm studies are presented for contaminated aquifer materials which were collected from a variety of industrial sites. These represent the following contaminant situations: perchloro-ethylene, trichloro-ethylene and their degradation products, 1,1,1-TCA and DCA and a site with a complex mixture of trichloro-ethene, cDCE, dichloro-methane, 1,1,1-TCA, 1,1-DCA, 1,2-dichloropropane, toluene, xylenes, 1,24-trimethylbenzene and mineral oil. The following electron donors were evaluated for their ability to stimulate halorespiration: lactate, methanol, ethanol, molasses and yeast extract. All of these carbon sources were found to stimulate biodegradation of chlorinated ethenes, but their relative performance was found to be site specific. For a number of sites, stagnation was observed at cDCE, for other sites complete conversion of PER and TRI to ethene was observed. Some aquifer materials were screened for the presence of genetic material of Dehalococcoides sp. by means of the polymerase chain reaction. Dehalococcoides sp. are believed to be required for complete reduction of perchloro-ethylene or trichloro-ethylene to ethene. A positive signal was found for aquifer material which exhibited formation of ethene, while soil material from another area at the same site which did not exhibit formation of ethene gave a negative PCR-signal. For two sites anaerobic biodegradation of 1,1,1-TCA could not be stimulated by addition of various carbon sources and it was also persistent under aerobic conditions for one site. Reductive dehalogenation of 1,1,1-TCA to DCA was rapid when zerovalent iron was used, but conversion of DCA was much slower. (orig.)

  12. Chlorinated hydrocarbon contaminants in arctic marine mammals.

    Science.gov (United States)

    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 (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. Lawrence and ringed seal in the Baltic Sea, indicate that overall contamination of the Arctic marine ecosystem is 10-50 times less than the most highly contaminated areas in the northern hemisphere temperate latitude marine environment. Geographic distribution of residue levels in polar bears

  13. Riverine input of chlorinated hydrocarbons in the coastal pollution

    Digital Repository Service at National Institute of Oceanography (India)

    Sarkar, A.; Everaarts, J.M.

    of various chlorinated hydrocarbons. It deals with an in-depth analysis of pollution of the coastal ecosystem around the Netherlands, U.K. and Germany due to inputs of contaminants from the rivers namely, Elbe, Weser, Ems Ijssel, Rhine, Meuse, Scheldt, Thames...

  14. Bioremediation of soils containing petroleum hydrocarbons, chlorinated phenols, and polycyclic aromatic hydrocarbons

    International Nuclear Information System (INIS)

    Seech, A.; Burwell, S.; Marvan, I.

    1994-01-01

    Bench-scale treatability investigations, pilot-scale and full-scale bioremediation projects were conducted to evaluate Daramend trademark bioremediation of soils containing petroleum hydrocarbons, heavy oils, paraffins, chlorinated phenols and polycyclic aromatic hydrocarbons (PAHs). Bench-scale investigations were conducted using glass microcosms. Pilot-scale and full-scale demonstrations were conducted at industrial sites and included treatment of excavated soils and sediments in on-site cells constructed using synthetic liners and covered by steel/polyethylene structures as well as in-situ treatment. A total of approximately 5,000 tons of soil was treated. The soil treatment included organic soil amendments, specialized tillage/aeration apparatus, and strict control of soil moisture. The amendments are composed of naturally-occurring organic materials prepared to soil-specific particle size distributions, nutrient profiles, and nutrient-release kinetics. Bench-scale work indicated that in refinery soil containing high concentrations of heavy oils, extractable hydrocarbon concentrations could be rapidly reduced to industrial clean-up criteria, and that the hydrocarbons were fully mineralized with release of CO 2

  15. Atmospheric chlorinated polycyclic aromatic hydrocarbons in East Asia.

    Science.gov (United States)

    Kakimoto, Kensaku; Nagayoshi, Haruna; Konishi, Yoshimasa; Kajimura, Keiji; Ohura, Takeshi; Hayakawa, Kazuichi; Toriba, Akira

    2014-09-01

    This study estimates atmospheric concentrations of chlorinated polycyclic aromatic hydrocarbons (ClPAHs) and polycyclic aromatic hydrocarbons (PAHs) in East Asia using a Gas Chromatograph with High Resolution Mass Spectrometer (GC-HRMS). ClPAHs are ubiquitously generated from PAHs through substitution, and some ClPAHs show higher aryl hydrocarbon receptor (AhR)-mediated activities than their parent PAHs. Atmospheric particles were collected using a high-volume air sampler equipped with a quartz-fiber filter. We determined the ClPAH concentrations of atmospheric particles collected in Japan (Sapporo, Sagamihara, Kanazawa, and Kitakyushu), Korea (Busan), and China (Beijing). The concentrations of ClPAHs were highest in the winter Beijing sample, where the total mean concentration was approximately 15-70 times higher than in the winter samples from Japan and Korea. The concentrations of Σ19ClPAHs and Σ9PAHs were significantly correlated in the Kanazawa and the Busan samples. This indicates that within those cities ClPAHs and PAHs share the same origin, implying direct chlorination of parent PAHs. Toxic equivalent concentrations (TEQs) of the total ClPAHs and PAHs were lowest in Kanazawa in the summer, reaching 1.18 and 2610fg-TEQm(-3) respectively, and highest in Beijing in the winter, reaching 627 and 4240000fg-TEQm(-3) respectively. Copyright © 2014 Elsevier Ltd. All rights reserved.

  16. Predicting the distribution of contamination from a chlorinated hydrocarbon release

    Energy Technology Data Exchange (ETDEWEB)

    Lupo, M.J. [K.W. Brown Environmental Services, College Station, TX (United States); Moridis, G.J. [Lawrence Berkeley Laboratory, Berkeley, CA (United States)

    1995-03-01

    The T2VOC model with the T2CG1 conjugate gradient package was used to simulate the motion of a dense chlorinated hydrocarbon plume released from an industrial plant. The release involved thousands of kilograms of trichloroethylene (TCE) and other chemicals that were disposed of onsite over a period of nearly twenty years. After the disposal practice ceased, an elongated plume was discovered. Because much of the plume underlies a developed area, it was of interest to study the migration history of the plume to determine the distribution of the contamination.

  17. Chlorinated hydrocarbons and PCBs in field soils, sediments and sewage sludges

    International Nuclear Information System (INIS)

    Schaaf, H.

    1992-01-01

    As requested by the Ministry of Agriculture of the FRG, the 'Verband Deutscher Landwirtschaftlicher Untersuchungs- und Forschungsanstalten (VDLUFA)' built up a data collection over chlorinated hydrocarbons and PCBs in field soils, sediments, sewage sludges. Nearly 70.000 samples were collected and statistically evaluated. The results of these investigations will be described. The major constituents of the chlorinated hydrocarbons generally were Lindane, DDT(total) and HCB. In sewage sludges PCBs could be detected in nearly every sample. The contents of PCBs in field soils are smaller than in sewage sludges. Rather 'high contents', greater than 100-200 μg/kg d.m./organic pollutants, were detected only in 2% of the samples. 7 refs., 5 figs., 2 tabs

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

    Science.gov (United States)

    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.

  19. Subsurface Transport of Hydrocarbon Fuel Additives and a Dense Chlorinated Solvent

    National Research Council Canada - National Science Library

    Guven, O

    1996-01-01

    This report provides a description of the work done at Auburn University for the research project 'Subsurface Transport of Hydrocarbon Fuel additives and a Chlorinated Solvent', supported by Armstrong...

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

    NARCIS (Netherlands)

    Hamonts, K.; Ryngaert, A.; Smidt, H.; Springael, D.; Dejonghe, W.

    2014-01-01

    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,

  1. Distribution of nonionic organic compounds (highly volatile chlorinated hydrocarbons) in the unsaturated zone

    Energy Technology Data Exchange (ETDEWEB)

    Grathwohl, P.

    1988-01-01

    Nonpolar pollutants, e.g. highly volatile chlorinated hydrocarbons (HVCH) are more or less equally distributed among all three soil phases (solids, water, air) in the unsaturated zone. The sorption of HVCH on soil solids depends on the amount and type of organic matter in the soil. For wet material an additional sorption on mineral surfaces can be neglected, since all possible sites for sorption are occupied by water. Provided the partition-coefficients or sorption-constants are known the contamination of the whole system can be evaluated from the pollutant concentration in the soil air; in addition it is possible to estimate a groundwater risk.

  2. Role of soot in the transport of chlorine in hydrocarbon-air diffusion flames

    International Nuclear Information System (INIS)

    Venkatesh, S.; Saito, K.; Stencel, J.M.; Majidi, V.; Owens, M.

    1991-01-01

    Soot is an inevitable product of incomplete combustion in many practical combustion systems such as automobiles, incinerators and furnaces. Recent studies on chlorinated hydrocarbon combustion have shown that soot and other praticulates (eg. fly ash) play an important role in secondary reactions leading to the formation of chlorine substituted polyaromatic hydrocarbons (PAHs). In order to attain very high destruction efficiencies the fundamental chemical and physical processes that are associated with combustion, and post-combustion cleanup must be well understood. In order to understand the effect of chlorine on the soot formed in a combustion system, fundamental studies using a coflow laminar hydrocarbon-air diffusion flame have been carried out. Phenomenological studies have revealed the effect of chlorine on the visible structure of the flame. Soot inception activation energies were estimated for methane, ethane and ethylene diffusion flames for the case of with and without chlorine addition. No significant difference in the activation energy was estimated for either case. The effect of chlorine on the soot escape rate of an acetylene diffusion flame was estimated. The soot formed in these diffusion flames was analyzed for chlorine using scanning electron microscopy with energy dispersive spectroscopy (SEM/EDS) and by laser induced plasma spectroscopy (LIPS). REsults from these techniques indicate the presence of chlorine in the soot formed. In this paper a chemical scheme to explain the chlorine found in the soot is proposed based on known theories of soot formation

  3. Microbial and molecular techniques to evaluate and to implement in-situ biodegradation potential and activity at sites contaminated with aromatic and chlorinated hydrocarbons

    International Nuclear Information System (INIS)

    Karg, F.; Henkler, Ch.

    2005-01-01

    (Biochemical Laboratory of the Medical Faculty) the first PBG-SP : 'Pole Biotechnologique et Genetique - Sites Pollues' in France. The modern tools and approaches have been applied successfully at several field sites for the evaluation, implementation and on-going monitoring of the bio-restoration/ attenuation of various aromatic and chlorinated compounds. (authors)

  4. Application of Pseudomonas sp. strain DCA1 for the removal of chlorinated hydrocarbons

    NARCIS (Netherlands)

    Hage, J.C.

    2004-01-01

    The large-scale application of chlorinated aliphatic hydrocarbons (CAHs) has resulted in many cases of groundwater contamination. Contaminated groundwater can be remediated by pump-and-treat: the groundwater is pumped to the surface and treated. The groundwater can be treated in bioreactors, in

  5. Anaerobic transformation of chlorinated hydrocarbons in a packed-bed reactor

    NARCIS (Netherlands)

    Best, Jappe Hinco de

    1999-01-01

    Chlorinated aliphatic hydrocarbons belong to the most frequently found contaminants in soil. Because of their toxicity and persistence, they are a potential threat to human health and the diversity of ecosystems. For the cleanup of soils contaminated with these compounds, biological degradation by

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

    Czech Academy of Sciences Publication Activity Database

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

    2015-01-01

    Roč. 112, Jul (2015), s. 108-116 ISSN 0969-806X R&D Projects: GA ČR GA13-28721S Institutional support: RVO:68378271 Keywords : chlorinated hydrocarbons * TCE * PCE * PCBs * dechlorination * gamma irradiation * modifiers * cell membrane permeability Subject RIV: CH - Nuclear ; Quantum Chemistry Impact factor: 1.207, year: 2015

  7. Kinetics of Chlorinated Hydrocarbon Degradation by Methylosinus trichosporium OB3b and Toxicity of Trichloroethylene

    NARCIS (Netherlands)

    Oldenhuis, Roelof; Oedzes, Johannes Y.; Waarde, Jacob J. van der; Janssen, Dick B.

    The kinetics of the degradation of trichloroethylene (TCE) and seven other chlorinated aliphatic hydrocarbons by Methylosinus trichosporium OB3b were studied. All experiments were performed with cells grown under copper stress and thus expressing soluble methane monooxygenase. Compounds that were

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

    Science.gov (United States)

    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. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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

    Science.gov (United States)

    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. Copyright © 2016 Elsevier B.V. All rights reserved.

  10. The effect of fuel and chlorinated hydrocarbons on a vapor phase carbon adsorption system

    International Nuclear Information System (INIS)

    Crawford, W.J.; Cheney, J.L.; Taggart, D.B.

    1995-01-01

    A soil vapor extraction (SVE) system installed at the South Tacoma Well 12A Superfund Site was designed to recover 1,2-dichloroethylene (DCE), trichloroethylene (TCE), tetrachloroethylene (PCE), and 1,1,2,2-tetrachloroethane (1,1,2,2-TCA) from the vadose zone. The basic system consisted of twenty-two extraction wells, three centrifugal blowers, and three carbon adsorbers. The carbon adsorbers were regenerated on site by steam stripping. The mixture of steam and stripped organics was condensed and then decanted to separate the water from the organic phase. The recovered water was air stripped to remove the dissolved organics prior to discharge to the city storm sewer. The recovered organic phase was then shipped off site for thermal destruction. Previous reports described operating difficulties with the decanter, and air strippers. Sampling and analyses were performed which identified the problem as the simultaneous recovery of unexpected fuel hydrocarbons in addition to the solvents. Recovery of fuels resulted in a light phase in the decanter in addition to the water and heavy solvent phases. This required redesign of the decanter to handle the third phase. The effectiveness of desorption of the carbon beds by steam stripping gradually decreased as the remediation progressed into the second year of operation. Samples were collected from the carbon beds to evaluate the effect of the fuel and chlorinated hydrocarbons on the activated carbon. This report describes the results of these analyses. The data indicated that both 1,1,2,2-TCA and fuel hydrocarbons in the C-9 to C-24 range remained in the carbon beds after steam regeneration in sufficient quantities to require replacing the carbon

  11. Application of compound specific 13C isotope investigations of chlorinated hydrocarbons in contaminated groundwaters

    International Nuclear Information System (INIS)

    Osenbrueck, K.; Heidinger, M.; Voropaev, A.; Ertl, S.; Eichinger, L.

    2002-01-01

    Full text: Chlorinated hydrocarbons are one of the most common pollutants found in groundwater. Due to complex contamination situations with overlapping contamination plumes the assessment of the organic contaminants requires the installation of expensive observation wells and high analytical effort. Here the determination of the stable isotope ratio 13 C/ 12 C of the organic compounds offers a promising and efficient tool to investigate the origin and the biodegradation characteristics of the chlorinated hydrocarbons in groundwater. The application of the method is based on characteristic isotope fingerprints, differing in chlorinated solvents. This isotope fingerprint is derived from different production pathways and is not influenced by transport or by retardation processes in the underground. Due to the fact, that two different contaminations can easily be distinguished by isotope ratios, an improved distinction of spatially and temporally different contamination plumes might be possible. In course of biologically mediated degradation processes a shift of the isotope ratios between the precursor and the product can frequently be observed, such as with denitrification or sulfate reduction processes. The isotope fractionation is due to a preferential reaction of the bonds formed by the lighter isotopes and leads to a progressive enrichment of the heavy isotopes in the precursor while the product becomes depleted in the heavy isotopes. Biological degradation of the highly chlorinated hydrocarbons is due to a co-metabolic dechlorinisation. Tetrachloroethene (PCE) for example degrades under anoxic conditions via trichloroethene (TCE) to cis-1,2-dichloroethene (cDCE). Subsequent degradation to vinyl chloride (VC) and ethene may appear under aerobic as well as reducing environments depending on the site specific conditions. In several laboratory studies it has been shown, that biodegradation of the chlorinated hydrocarbons is accompanied by an isotope fractionation of

  12. Performance studies of an IR fiber optic sensor for chlorinated hydrocarbons in water

    International Nuclear Information System (INIS)

    Goebel, R.; Krska, R.; Neal, S.; Kellner, R.

    1994-01-01

    Chlorinated hydrocarbons (CHCs) were monitored using a recently presented infrared fiber-optic physico-chemical sensor consisting of an MIR transparent, polymer coated, silver halide fiber coupled to a commercial FTIR spectrometer. The aim of this study was to test the performance of this new fiber optic sensing device with respect to temperature dependence, simultaneous detection of several CHCs, sensitivity and dynamic response behavior. In addition the diffusion process of the CHCs into the polymer was analyzed in order to better understand and evaluate the obtained results. During the investigation of the temperature dependence of the sensor response to real trend could be observed in the temperature range of 0 to 22 C. The dynamic response of the sensor is in the minute range when experiencing an increase in concentration of the analyte while with a decrease in concentration, the response is relatively slow. The sensor enabled the detection of 10 environmentally relevant CHCs at concentrations of 1 to 50 ppm. The simulation of the experimental diffusion data revealed Fick's 1st law diffusion for CHCs into the polymer layers. Finally the sensing device was validated with head spacegas chromatography (HSGC) analyses and showed good agreement with these already established methods. This work shows the great potential of IR fiber optic sensors as early warning systems for a variety of CHCs in water (''threshold alarm sensor'') (orig.)

  13. The use of DNA technologies in determining the biotreatability of chlorinated aliphatic hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Douglas, A. [HydroQual, Calgary, AB (Canada)

    2008-07-01

    HydroQual Laboratories is a wholly-owned subsidiary of Golder Associates and uses biological testing for measuring the effect of toxins and their impact on various links in the food chain in order to evaluate and improve environmental health. It has expertise in various fields of the natural sciences and is ISO certified. This presentation discussed the use of DNA technologies in determining the biotreatability of chlorinated aliphatic hydrocarbons. The paper presented biotreatability studies run by the company which included bench scale testing on various types of contaminants. The testing involved multiple treatments, determination of dosage, and additional amendments. The strategy may vary based on bench test results and legislation. Trichloroethylene/perchloroethylene remediation strategies were also presented for chemical oxidation; aerobic bioremediation; abiotic remediation; and anaerobic biostimulation and augmentation. Biostimulation was defined as the addition of nutrients to influence the redox potential. The presentation also reviewed anaerobic dehalorespiration; detection methods; DNA isolation; polymerase chain reaction (PCR); and biotreatability case studies. The presentation concluded with some future directions and other uses of PCR. tabs., figs.

  14. Evaluation of hydrocarbon potential

    International Nuclear Information System (INIS)

    Cashman, P.H.; Trexler, J.H. Jr.

    1992-01-01

    Task 8 is responsible for assessing the hydrocarbon potential of the Yucca Mountain vincinity. Our main focus is source rock stratigraphy in the NTS area in southern Nevada. (In addition, Trexler continues to work on a parallel study of source rock stratigraphy in the oil-producing region of east central Nevada, but this work is not funded by Task 8.) As a supplement to the stratigraphic studies, we are studying the geometry and kinematics of deformation at NTS, particularly as these pertain to reconstructing Paleozoic stratigraphy and to predicting the nature of the Late Paleozoic rocks under Yucca Mountain. Our stratigraphic studies continue to support the interpretation that rocks mapped as the open-quotes Eleana Formationclose quotes are in fact parts of two different Mississippian units. We have made significant progress in determining the basin histories of both units. These place important constraints on regional paleogeographic and tectonic reconstructions. In addition to continued work on the Eleana, we plan to look at the overlying Tippipah Limestone. Preliminary TOC and maturation data indicate that this may be another potential source rock

  15. Biodegradation of chlorinated hydrocarbons in a vapor phase reactor

    International Nuclear Information System (INIS)

    Ensley, B.D.

    1992-01-01

    A bench scale gas lift loop reactor was constructed to evaluate the feasibility of trichloroethylene (TCE) degradative microorganisms being used to treat TCE contaminated air. Two different microorganisms were used as biocatalysts in this reactor. After proper operating conditions were established for use of this reactor/biocatalyst combination, both microorganisms could degrade 95% of inlet TCE at air flow rates of up to 3% of the total reactor volume per minute. TCE concentrations of between 300 μg/L (60ppmv) and 3000 μg/L (600 ppmv) were degraded with 95% or better efficiency. Preliminary economic evaluations suggest that bioremediation may be the low cost alternative for treating certain TCE contaminated air streams and field trials of a scaled-up reactor system based on this technology are currently underway

  16. Internal laboratory control in residue analysis of chlorinated hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    1980-01-01

    The thesis contains a chapter on gaschromatographic system in which gas current, temperatures, separation system, detector system, recorder, dosing system and integrator are described. The chapter on reagents deals with standards and solvents, absorbents and other reagents. The chapter on laboratory equipment deals with general recommendations for apparatus, purification and total numerical result of blank test. The chapter ''Methods'' contains general references, aptitude for a special problem, common investigations and control by standard reference materials. The chapter on the work up of samples treats extraction, purification, concentrating the solution, internal standard, multiple determination and control samples. The chapter on measurement presents calibration, internal standard, multiple determination, securing the result and control samples. The chapter on evaluation consists of qualitative and quantitave evaluation, decision criteria and communication of the result. The chapter of documentation described routine investigations, tests and controls of internal laboratory control, preliminary works, maintenance and service works.

  17. Analytical method development using functionalized polysulfone membranes for the determination of chlorinated hydrocarbons in water.

    Science.gov (United States)

    Nuhu, Abdulmumin A; Basheer, Chanbasha; Abu-Thabit, Nedal Y; Alhooshani, Khalid; Al-Arfaj, Abdul Rahman

    2011-12-15

    In this study, functionalized polysulfone membrane has been utilized as a sorbent for the extraction of chlorinated hydrocarbons (CHCs) in water samples. Two different functionalized polysulfones (i) phosphonic acid functionalized polysulfone (PPSU-A) with different forms (cross-linked and non cross-linked) membranes and (ii) phosphonic ester functionalized polysulfone (PPSU-E) with different forms (cross-linked and non cross-linked) were evaluated for the extraction of CHCs in water. A 10 ml of spiked water sample was extracted with 50mg piece of the functionalized membrane. After extraction, the membrane was desorbed by organic solvent and the extract was analyzed by gas chromatography-mass spectrometry. Eight CHCs, 1,3,5-trichlorobenzene (1,3,5-TCB), 1,2,3-trichlorobenzene (1,2,3-TCB), 1,1,2,3,4,4-hexachloro-1,3-butadiene (HCBD), 1,2,4-trichloro-3-methylbenzene (TCMB), 1,2,3,4-tetrachlorobenzene (1,2,3,4-TeCB), 1,2,4,5-tetrachlorobenzene (1,2,4,5-TeCB), pentachlorobenzene (PeCB) and hexachlorobenzene (HCB) were used as model compounds. Experimental parameters such as extraction time, desorption time, types of polymer membrane as well the nature of desorption solvent were optimized. Using optimum extraction conditions calibration curves were linear with coefficients of determination between 0.9954 and 0.9999 over wide range of concentrations (0.05-100 μgl(-1)). The method detection limits (at a signal-to-noise ratio of 3) were in the range of 0.4-3.9 ng l(-1). The proposed method was evaluated for the determination of CHCs in drinking water samples. Copyright © 2011 Elsevier B.V. All rights reserved.

  18. Determination of chlorinated hydrocarbons in single and multi component test gases

    Energy Technology Data Exchange (ETDEWEB)

    Giese, U.; Stenner, H. (Paderborn Univ. (Gesamthochschule) (Germany, F.R.). Angewandte Chemie); Ludwig, E.; Kettrup, A. (Paderborn Univ. (Gesamthochschule) (Germany, F.R.). Angewandte Chemie Gesellschaft fuer Strahlen- und Umweltforschung mbH Muenchen, Neuherberg (Germany, F.R.). Inst. fuer Oekologische Chemie)

    1990-11-01

    For comparing the efficiency of active and diffusive sampling methods two diffusive samplers with different properties were used to determine chlorinated hydrocarbons (CH{sub 2}Cl{sub 2}, CHCl{sub 3}, CCl{sub 4}) in single and multi component test gas mixtures. One of the chosen diffusive samplers can also be used for active sampling. In general, good correlations of all tested methods could be observed in the direct comparison of active and diffusive sampling and in the determination of the efficiencies. During the application of active and diffusive sampling methods in multi component test gases of the analytes possible interferences could not be ascertained. (orig.).

  19. Volatile Short-chain Chlorinated Hydrocarbons in the Groundwater of the City of Zagreb

    OpenAIRE

    Marijanović-Rajčić, M.; Senta, A.

    2008-01-01

    The aim of the study was to assess the quality of the groundwater sampled from private wells and the public water-supply system in terms of estimating the contamination caused by short-chain chlorinated hydrocarbons, as well as to estimate the exposure of the citizens dwelling in different suburbs to these pollutants of their drinking water (Fig. 1). The aim of the study was also to determine which suburb is supplied through the public water-supply system with water originating from the Sašna...

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

    Science.gov (United States)

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

    2014-12-01

    Chlorinated aliphatic hydrocarbons (CAHs) are common groundwater contaminants that can be removed from the environment by natural attenuation processes. CAH biodegradation can occur in wetland environments by reductive dechlorination as well as oxidation pathways. In particular, CAH oxidation may occur in vegetated wetlands, by microorganisms that are naturally associated with the roots of wetland plants. The main objective of this study was to evaluate the cometabolic degradation kinetics of the CAHs, cis-1,2-dichloroethene (cisDCE), trichloroethene (TCE), and 1,1,1-trichloroethane (1,1,1TCA), by methane-oxidizing bacteria associated with the roots of a typical wetland plant in soil-free system. Laboratory microcosms with washed live roots investigated aerobic, cometabolic degradation of CAHs by the root-associated methane-oxidizing bacteria at initial aqueous [CH4] ~ 1.9 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.

  1. Application of novel activated carbon fiber solid-phase, microextraction to the analysis of chlorinated hydrocarbons in water by gas chromatography-mass spectrometry

    International Nuclear Information System (INIS)

    Sun Tonghua; Jia Jinping; Fang Nenghu; Wang Yalin

    2005-01-01

    This paper presents a study on the performance of activated carbon fiber (ACF) used as extraction fiber for solid-phase microextraction (SPME) and its application for analysis of chlorinated hydrocarbons in water. By means of evaluating scanning electron microscope (SEM) images, specific surface area, pore volume, pore distribution, and properties of adsorption and desorption, the optimal active concentration of phosphoric acid has been determined. Coupled with gas chromatograph-mass spectrometry (GC-MS), ACF-SPME is suitable for determination chlorinated hydrocarbons in water with headspace. Experimental parameters such as adsorption and desorption conditions were studied. The optimized method has an acceptable linearity, good precision, with R.S.D. values <10% for each compound. Compared with commercial fibers, ACF has many advantages such as better resistance to organic solvents, better endurance to high temperature and longer lifetime

  2. Biotransformation of monoaromatic and chlorinated hydrocarbons at an aviation-gasoline spill site

    International Nuclear Information System (INIS)

    Wilson, B.H.; Wilson, J.T.; Kampbell, D.H.; Bledsoe, B.E.; Armstrong, J.M.

    1991-01-01

    Loss of petroleum products from underground storage tanks, pipelines, and accidental spills are major sources of contamination of unsaturated soils, aquifer solids, and 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 a chlorinated solvent spill adjacent to the aviation gasoline spill. The groundwater is buffered near neutrality. The aviation gasoline plume is methanogenic and the aquifer contains enough iron minerals to support significant iron solubilization. Field evidence of both aerobic and anaerobic biotransformation of monoaromatics was confirmed by laboratory studies of aquifer material obtained from the site. In the laboratory studies, the removal of the monoaromatics in the anaerobic material was rapid and compared favorable with removal in the aerobic material. The kinetics of anaerobic removal of monoaromatics in the laboratory were similar to the kinetics at field scale in the aquifer. Biotransformation of the chlorinated solvents was not observed until late in the study, when daughter products from reductive dechlorination of the chlorinated solvents were identified by GC/MS

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

    Science.gov (United States)

    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.

  4. WHIM-3D-QSPR APPROACH FOR PREDICTING AQUEOUS SOLUBILITY OF CHLORINATED HYDROCARBONS

    Directory of Open Access Journals (Sweden)

    Oman Zuas

    2010-06-01

    Full Text Available The weighted holistic invariant molecular-three dimensional-quantitative structure property relationship (WHIM-3D-QSPR approach has been applied to the study of the aqueous solubility (- log Sw of chlorinated hydrocarbon compounds (CHC's. The obtained QSPR model is predictive and only requires four WHIM-3D descriptors in the calculation. The correlation equation of the model that is based on a training set of 50 CHC's compound has statistical parameters: standard coefficient correlation (R2 = 0.948; cross-validated correlation coefficients (Q2 = 0.935; Standard Error of Validation (SEV = 0.35; and average absolute error (AAE = 0.31. The application of the best model to a testing set of 50 CHC's demonstrates a reliable result with good predictability. Besides, it was possible to construct new model by applying WHIM-3D-QSPR approach without require any experimental physicochemical properties in the calculation of aqueous solubility.   Keywords: WHIM-3D; QSPR; aqueous solubility; - Log Sw, chlorinated hydrocarbons, CHC's

  5. Rush-hour aromatic and chlorinated hydrocarbons in selected subway stations of Shanghai, China.

    Science.gov (United States)

    Zhang, Yanli; Li, Chunlei; Wang, Xinming; Guo, Hai; Feng, Yanli; Chen, Jianmin

    2012-01-01

    Air samples were collected simultaneously at platform, mezzanine and outdoor in five typical stations of subway system in Shanghai, China using stainless steel canisters and analyzed by gas chromatography-mass selective detector (GC-MSD) after cryogenic preconcentration. Benzene, toluene, ethylbenzene and xylenes (BTEX) at the platforms and mezzanines inside the stations averaged (10.3 +/- 2.1), (38.7 +/- 9.0), (19.4 +/- 10.1) and (30.0 +/- 11.1) microg/m3, respectively; while trichloroethylene (TrCE), tetrachloroethylene (TeCE) and para-dichlorobenzene (pDCB), vinyl chloride and carbon tetrachloride were the most abundant chlorinated hydrocarbons inside the stations with average levels of (3.6 +/- 1.3), (1.3 +/- 0.5), (4.1 +/- 1.1), (2.2 +/- 1.1) and (1.2 +/- 0.3) microg/m3, respectively. Mean levels of major aromatic and chlorinated hydrocarbons were higher indoor (platforms and mezzanines) than outdoor with average indoor/outdoor (I/O) ratios of 1.1-9.5, whereas no significant indoor/outdoor differences were found except for benzene and TrCE. The highly significant mutual correlations (p subway stations from indoor/outdoor air exchange and traffic emission should be their dominant source. TrCE and pDCB were mainly from indoor emission and TeCE might have both indoor emission sources and contribution from outdoor air, especially in the mezzanines.

  6. Analysis of dechlorination kinetics of chlorinated aliphatic hydrocarbons by Fe(II) in cement slurries

    Energy Technology Data Exchange (ETDEWEB)

    Jung, Bahngmi [Department of Earth and Environmental Sciences, Wright State University, Dayton, OH 45435-0001 (United States)], E-mail: jung.bahngmi@gmail.com; Batchelor, Bill [Department of Civil Engineering, Texas A and M University, College Station, TX 77843-3136 (United States)

    2008-03-21

    Degradative solidification/stabilization with ferrous iron (DS/S-Fe(II)) has been found to be effective in degrading a number of chlorinated aliphatic hydrocarbons including 1,1,1-trichloroethane (1,1,1-TCA), 1,1,2,2-tetrachloroethane (1,1,2,2-TeCA), tetrachloroethylene (PCE), trichloroethylene (TCE), 1,1-dichloroethylene (1,1-DCE), vinyl chloride (VC), carbon tetrachloride (CT) and chloroform (CF). Previous studies have characterized degradation kinetics in DS/S-Fe(II) systems as affected by Fe(II) dose, pH and initial target organic concentration. The goal of this study is to investigate the importance of various chemical properties on degradation kinetics of DS/S-Fe(II). This was accomplished by first measuring rate constants for degradation of 1,1,1-TCA, 1,1,2,2-TeCA and 1,2-dichloroethane (1,2-DCA) in individual batch experiments. Rate constants developed in these experiments and those obtained from the literature were related to thermodynamic parameters including one-electron reduction potential, two-electron reduction potential, bond dissociation energy and lowest unoccupied molecular orbital energies. Degradation kinetics by Fe(II) in cement slurries were generally represented by a pseudo-first-order rate law. The results showed that the rate constants for chlorinated methanes (e.g. CT, CF) and chlorinated ethanes (e.g. 1,1,1-TCA) were higher than those for chlorinated ethylenes (e.g. PCE, TCE, 1,1-DCE and VC) under similar experimental conditions. The log of the pseudo-first-order rate constant (k) was found to correlate better with lowest unoccupied molecular orbital energies (E{sub LUMO}) (R{sup 2} = 0.874) than with other thermodynamic parameter descriptors.

  7. Chlorine

    Science.gov (United States)

    ... your clothing, rapidly wash your entire body with soap and water, and get medical care as quickly as possible. Removing and disposing of clothing: Quickly take off clothing that has liquid chlorine on it. Any clothing that has to ...

  8. In situ bioremediation of petroleum hydrocarbons and chlorinated hydrocarbons: Three case studies

    International Nuclear Information System (INIS)

    Bost, R.C.; Perry, R.G.; Barber, T.

    1997-01-01

    In situ biodegradation of organic contaminants is one of the most cost-effective means of site remediation. This method has proven successful in soils, ground water, and slurries. Bacteria capable of degrading organic contaminants within an aquifer include many species from a wide spectrum of genera, e.g. Pseudomonas, Corynebacterium, Bacillus, etc. In most cases, a mixture of bacterial strains is required to completely oxidize a complex organic contaminant. Each strain of an organism may target a specific compound, working together with other organisms to ultimately degrade each intermediate until complete degradation, also known as mineralization, occurs. One or more of the following mechanisms are utilized by bacteria for organic chemical degradation: (1) aerobic, (2) anaerobic, and (3) co-metabolic. During aerobic oxidation of organic chemicals, bacteria utilize the pollutant as an electron and hydrogen source and oxygen acts as the electron and hydrogen acceptor, resulting in water. As the bacterial enzymes cleave the compound, oxidized products are produced along with energy for the reaction to proceed. This is the most rapid and widely utilized mechanism. Dehalogenation occurs under aerobic, or perhaps more often, under anoxic conditions. This process occurs in the presence of alternate electron acceptors and replaces chlorine with hydrogen. The mechanism of co-metabolism can be aerobic or anaerobic, but is more often aerobic. This process requires a separate energy source for the bacterial cell because the pollutant is not utilized as an energy source. The role of bioremediation in site remediation is demonstrated below by three case studies: (1) a refinery, (2) a municipal landfill and (3) a pesticide formulation plant

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

    NARCIS (Netherlands)

    Hamonts, K.; Kuhn, T.; Vos, J.; Maesen, M.; Kalka, H.; Smidt, H.; Springael, D.; Meckenstock, R.U.; Dejonghe, W.

    2012-01-01

    Chlorinated aliphatic hydrocarbons (CAHs) often discharge into rivers as contaminated groundwater base flow. Biotrans formation, 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

  10. MULTICOMPONENT DETERMINATION OF CHLORINATED HYDROCARBONS USING A REACTION-BASED CHEMICAL SENSOR .2. CHEMICAL SPECIATION USING MULTIVARIATE CURVE RESOLUTION

    NARCIS (Netherlands)

    Tauler, R.; Smilde, A. K.; HENSHAW, J. M.; BURGESS, L. W.; KOWALSKI, B. R.

    1994-01-01

    A new multivariate curve resolution method that can extract analytical information from UV/visible spectroscopic data collected from a reaction-based chemical sensor is proposed. The method is demonstrated with the determination of mixtures of chlorinated hydrocarbons by estimating the kinetic and

  11. Adsorption of chlorinated hydrocarbons from aqueous solutions by wetted and non-wetted synthetic sorbents:dynamics

    NARCIS (Netherlands)

    Rexwinkel, G.; Rexwinkel, Glenn; Berkhout, J.T.A.M.; Heesink, Albertus B.M.

    2003-01-01

    In the present investigation the dynamics of the adsorption of several chlorinated hydrocarbons onto wetted and non-wetted synthetic sorbents was studied. A single particle model was developed to describe the adsorption behavior. The values of the mass transfer coefficient, needed to describe the

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

    Science.gov (United States)

    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.; hide

    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

  13. Unsaturated medium hydrocarbons pollution evaluation

    International Nuclear Information System (INIS)

    Di Luise, G.

    1991-01-01

    When the so called porous unsaturated medium, that's the vertical subsoil section between both the ground and water-table level, is interested by a hydrocarbons spill, the problem to evaluate the pollution becomes difficult: considering, essentially, the natural coexistence in it of two fluids, air and water, and the interactions between them. This paper reports that the problems tend to increase when a third fluid, the pollutant, immiscible with water, is introduced into the medium: a three-phases flow, which presents several analogies with the flow conditions present in an oil-reservoir, will be established. In such a situation, it would be very useful to handle the matter by the commonly used parameters in the oil reservoirs studies such as: residual saturation, relative permeability, phases mobility, to derive a first semiquantitative estimation of the pollution. The subsoil pollution form hydrocarbons agents is one of the worldwide more diffused causes of contamination: such events are generally referable to two main effects: accidental (oil pipeline breakdowns, e.g.), and continuous (underground tanks breaks, industrial plants leakages, e.g.)

  14. Volatile Short-chain Chlorinated Hydrocarbons in the Groundwater of the City of Zagreb

    Directory of Open Access Journals (Sweden)

    Marijanović-Rajčić, M.

    2008-01-01

    Full Text Available The aim of the study was to assess the quality of the groundwater sampled from private wells and the public water-supply system in terms of estimating the contamination caused by short-chain chlorinated hydrocarbons, as well as to estimate the exposure of the citizens dwelling in different suburbs to these pollutants of their drinking water (Fig. 1. The aim of the study was also to determine which suburb is supplied through the public water-supply system with water originating from the Sašnak spring that is contaminated with volatile chlorinated short-chain hydrocarbons.Drinking water samples were taken from 3 private wells and 1 public water-supply system situated in 3 Zagreb suburbs - Pešćenica, Trnje, and Trešnjevka. The sampling was carried out during 2003 and was undertaken on a seasonal basis. Short-chain chlorinated hydrocarbons - 1,1,1-trichloroethane, carbon tetrachloride, 1,1,2-trichloroethene and 1,1,2,2-tetrachloroethene - were determined by gas chromatography, following "liquid-liquid extraction" in pentane. For that purpose, we applied the gas chromatograph equipped with an electron-capture detector, thermo-programmable operations, and a suitable capillary column. The technique applied was that of split-injection.The groundwater of the City of Zagreb was found to be contaminated with volatile chlorinated hydrocarbons. The concentration level of 1,1,1-trichloroethane, determined in most of the samples, was found to be low (Fig. 2. On the other hand, 1,1,2-trichloroethene was present in all samples in concentrations of about 1 µg l-1- (Fig. 3. Only the drinking water samples taken from private wells in the suburb of Trnje contained somewhat higher mass concentrations of 1,1,1-trichloroethane, with the peak value of 19.03 µg l-1, measured in the winter season. In the samples taken from private wells in Trnje, the mass concentrations of 1,1,2,2-tetrachloroethene rangedfrom 15.30 µg l-1 to 18.65 µg l-1, as measured in autumn

  15. SCENARIOS EVALUATION TOOL FOR CHLORINATED SOLVENT MNA

    Energy Technology Data Exchange (ETDEWEB)

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

    2006-08-16

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

  16. IN SITU DESTRUCTION OF CHLORINATED HYDROCARBON COMPOUNDS IN GROUNDWATER USING CATALYTIC REDUCTIVE REDUCTIVE DEHALOGENATION IN A REACTIVE WELL: TESTING AND OPERATIONAL EXPERIENCES. (R825421)

    Science.gov (United States)

    A groundwater treatment technology based on catalytic reductive dehalogenation has been developed to efficiently destroy chlorinated hydrocarbons in situ using a reactive well approach. The treatment process utilizes dissolved H2 as an electron donor, in...

  17. In situ sensing of subsurface contamination--part I: near-infrared spectral characterization of alkanes, aromatics, and chlorinated hydrocarbons.

    Science.gov (United States)

    Klavarioti, Maria; Kostarelos, Konstantinos; Pourjabbar, Anahita; Ghandehari, Masoud

    2014-05-01

    There is an imperative need for a chemical sensor capable of remote, in situ, long-term monitoring of chemical species at sites containing toxic chemical spills, specifically at chemical waste dumps, landfills, and locations with underground storage tanks. In the current research, a series of experiments were conducted measuring the near-infrared optical absorption of alkanes, aromatics, and chlorinated hydrocarbons. A spectral library was then developed to characterize the optical spectra of liquid hydrocarbons. Near-infrared analysis was chosen due to compatibility with optical fibers. The goal was to differentiate between classes of hydrocarbons and to also discriminate between compounds within a class of similar molecular structures. It was observed that unique absorption spectra can be obtained for each hydrocarbon, and this uniqueness can be used to discriminate between hydrocarbons from different families. Statistical analyses, namely, principal component analysis (PCA) and correlation coefficient (Spearman and Pearson methods), were attempted to match absorption spectra from an unknown hydrocarbon with the database with limited success. An algorithm was subsequently written to identify the characteristic peaks of each hydrocarbon that could be used to match data from an unknown chemical species with the database.

  18. Anaerobic Transformation of Chlorinated Aliphatic Hydrocarbons in a Sand Aquifer Based on Spatial Chemical Distributions

    Science.gov (United States)

    Semprini, Lewis; Kitanidis, Peter K.; Kampbell, Don H.; Wilson, John T.

    1995-04-01

    We estimated the distribution of chlorinated aliphatic hydrocarbons (CAHs) from groundwater samples collected along three transects in a sand aquifer. Trichloroethylene (TCE) leaked and contaminated the aquifer probably more than a decade before we collected the measurements. The data show significant concentrations of TCE, cis-l,2-dichloroethylene (c-DCE), vinyl chloride (VC), and ethene. We attributed DCE, VC, and ethene to the reductive dehalogenation of TCE. The CAH concentrations varied significantly with depth and correlate with sulfate and methane concentrations. Anoxic aquifer conditions exist with methane present at relatively high concentrations at depth. High concentrations of TCE correspond with the absence of methane or low methane concentrations, whereas products of TCE dehalogenation are associated with higher methane concentrations and low sulfate concentrations. Indications are that the dechlorination of TCE and DCE to VC and ethene is associated with sulfate reduction and active methanogenesis. TCE dechlorination to DCE is likely occurring under the less reducing conditions of sulfate reduction, with further reductions to VC and ethene occurring under methanogenic conditions. We estimated that about 20% of TCE has dechlorinated to ethene. The analysis of the data enhanced our knowledge of natural in situ transformation and transport processes of CAHs.

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

    Science.gov (United States)

    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.

  20. A metabolomics strategy to assess the combined toxicity of polycyclic aromatic hydrocarbons (PAHs) and short-chain chlorinated paraffins (SCCPs).

    Science.gov (United States)

    Wang, Feidi; Zhang, Haijun; Geng, Ningbo; Ren, Xiaoqian; Zhang, Baoqin; Gong, Yufeng; Chen, Jiping

    2018-03-01

    The combined toxicity of mixed chemicals is usually evaluated according to several specific endpoints, and other potentially toxic effects are disregarded. In this study, we provided a metabolomics strategy to achieve a comprehensive understanding of toxicological interactions between mixed chemicals on metabolism. The metabolic changes were quantified by a pseudotargeted analysis, and the types of combined effects were quantitatively discriminated according to the calculation of metabolic effect level index (MELI). The metabolomics strategy was used to assess the combined effects of polycyclic aromatic hydrocarbons (PAHs) and short-chain chlorinated paraffins (SCCPs) on the metabolism of human hepatoma HepG2 cells. Our data suggested that exposure to a combination of PAHs and SCCPs at human internal exposure levels could result in an additive effect on the overall metabolism, whereas diverse joint effects were observed on various metabolic pathways. The combined exposure could induce a synergistic up-regulation of phospholipid metabolism, an additive up-regulation of fatty acid metabolism, an additive down-regulation of tricarboxylic acid cycle and glycolysis, and an antagonistic effect on purine metabolism. SCCPs in the mixture acted as the primary driver for the acceleration of phospholipid and fatty acid metabolism. Lipid metabolism disorder caused by exposure to a combination of PAHs and SCCPs should be an important concern for human health. Copyright © 2017 Elsevier Ltd. All rights reserved.

  1. Scenarios Evaluation Tool for Chlorinated Solvent MNA

    Energy Technology Data Exchange (ETDEWEB)

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

    2007-02-28

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

  2. A statistical approach to evaluate hydrocarbon remediation in the unsaturated zone

    International Nuclear Information System (INIS)

    Hajali, P.; Marshall, T.; Overman, S.

    1991-01-01

    This paper presents an evaluation of performance and cleanup effectiveness of a vapor extraction system (VES) in extracting chlorinated hydrocarbons and petroleum-based hydrocarbons (mineral spirits) from the unsaturated zone. The statistical analysis of soil concentration data to evaluate the VES remediation success is described. The site is a former electronics refurbishing facility in southern California; soil contamination from organic solvents was found mainly in five areas (Area A through E) beneath two buildings. The evaluation begins with a brief description of the site background, discusses the statistical approach, and presents conclusions

  3. Site-specific probabilistic ecological risk assessment of a volatile chlorinated hydrocarbon-contaminated tidal estuary.

    Science.gov (United States)

    Hunt, James; Birch, Gavin; Warne, Michael St J

    2010-05-01

    Groundwater contaminated with volatile chlorinated hydrocarbons (VCHs) was identified as discharging to Penrhyn Estuary, an intertidal embayment of Botany Bay, New South Wales, Australia. A screening-level hazard assessment of surface water in Penrhyn Estuary identified an unacceptable hazard to marine organisms posed by VCHs. Given the limitations of hazard assessments, the present study conducted a higher-tier, quantitative probabilistic risk assessment using the joint probability curve (JPC) method that accounted for variability in exposure and toxicity profiles to quantify risk (delta). Risk was assessed for 24 scenarios, including four areas of the estuary based on three exposure scenarios (low tide, high tide, and both low and high tides) and two toxicity scenarios (chronic no-observed-effect concentrations [NOEC] and 50% effect concentrations [EC50]). Risk (delta) was greater at low tide than at high tide and varied throughout the tidal cycle. Spatial distributions of risk in the estuary were similar using both NOEC and EC50 data. The exposure scenario including data combined from both tides was considered the most accurate representation of the ecological risk in the estuary. When assessing risk using data across both tides, the greatest risk was identified in the Springvale tributary (delta=25%)-closest to the source area-followed by the inner estuary (delta=4%) and the Floodvale tributary (delta=2%), with the lowest risk in the outer estuary (delta=0.1%), farthest from the source area. Going from the screening level ecological risk assessment (ERA) to the probabilistic ERA changed the risk from unacceptable to acceptable in 50% of exposure scenarios in two of the four areas within the estuary. The probabilistic ERA provided a more realistic assessment of risk than the screening-level hazard assessment. Copyright (c) 2010 SETAC.

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

    Energy Technology Data Exchange (ETDEWEB)

    Elliott, J.E. [Canadian Wildlife Service, Pacific Wildlife Research Centre, 5421 Robertson Rd., RR no. 1, Delta, British Columbia, V4K 3N2 (Canada)]. E-mail: john.elliott@ec.gc.ca; Miller, M.J. [Iolaire Ecological Consulting, 7899 Thrasher St., Mission, British Columbia, V2V 5H3 (Canada); Wilson, L.K. [Canadian Wildlife Service, Pacific Wildlife Research Centre, 5421 Robertson Rd., RR no. 1, Delta, British Columbia, V4K 3N2 (Canada)

    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. - Based on the level of DDE contamination of prey items, it seems unlikely that peregrine falcons could breed successfully throughout most of the Okanagan Valley of British Columbia.

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

    Science.gov (United States)

    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 (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.

  6. Molecular mechanisms in the pyrolysis of unsaturated chlorinated hydrocarbons: formation of benzene rings. 1. Quantum chemical studies.

    Science.gov (United States)

    McIntosh, Grant J; Russell, Douglas K

    2013-05-23

    Analogues of important aromatic growth mechanisms in hydrocarbon pyrolysis and combustion systems are extended to chlorinated systems. We consider the addition of C2Cl2 to both C4Cl3 and C4Cl5 radicals at the M06-2X/6-311+G(3df,3p)//B3LYP/6-31G(d) level of theory, and we demonstrate that these reaction systems have much in common with those of nonchlorinated species. In particular, we find that these radicals appear to lead preferentially to fulvenes, and not to the observed aromatic products, as is found in nonchlorinated systems. We have therefore also considered nonradical C4/C2 channels by way of Diels-Alder cyclization of C4Cl4/C2Cl2 and C4H2Cl2/C2HCl pairs to describe aromatic formation. While the latter pair readily leads to the formation of partially chlorinated benzenes, the fully chlorinated congeners are sterically prohibited from ring closing directly; this leads to a series of novel rearrangement processes which predict the formation of hexachloro-1,5-diene-3-yne, in addition to hexachlorobenzene, in good agreement with experiment. This suggests, for the first time, that facile nonradical routes to aromatic formation are operative in partially and fully chlorinated pyrolysis and combustion systems.

  7. Comparison of atmosphere/aquatic environment concentration ratio of volatile chlorinated hydrocarbons between temperate regions and Antarctica.

    Science.gov (United States)

    Zoccolillo, Lelio; Amendola, Luca; Insogna, Susanna

    2009-09-01

    For the purpose of understanding the transport and deposition mechanisms and the air-water distribution of some volatile chlorinated hydrocarbons (VCHCs), their atmosphere/aquatic environment concentration ratio was evaluated. In addition, for the purpose of differentiating VCHC behaviour in a temperate climate from its behaviour in a polar climate, the atmosphere/aquatic environment concentration ratio evaluated in matrices from temperate zones was compared with the concentration ratio evaluated in Antarctic matrices. In order to perform air samplings also at rigid Antarctic temperatures, the sampling apparatus, consisting of a diaphragm pump and canisters, was suitably modified. Chloroform, 1,1,1-trichloroethane, tetrachloromethane, 1,1,2-trichloroethylene and tetrachloroethylene were measured in air, water and snow using specific techniques composed of a purpose-made cryofocusing-trap-injector (for air samples) and a modified purge-and-trap injector (for aqueous samples) coupled to a gas chromatograph with mass spectrometric detection operating in selected ion monitoring mode. The VCHCs were retrieved in all the investigated matrices, both Italian and Antarctic, with concentrations varying from tens to thousands of ng m(-3) in air and from digits to hundreds of ng kg(-1) in water and snow. The atmosphere/aquatic environment concentration ratios were always found to be lower than 1. In particular, the Italian air/water concentration ratios were smaller than the Antarctic ones, by reason of the higher atmospheric photochemical activity in temperate zones. On the other hand, the Antarctic air/snow concentration ratios proved to be largely in favour of snow with respect to the Italian ratios, thus corroborating the hypothesis of a more efficient VCHC deposition mechanism and accumulation on Antarctic snow.

  8. Technical Protocol for Using Soluble Carbohydrates to Enhance Reductive Dechlorination of Chlorinated Aliphatic Hydrocarbons

    Science.gov (United States)

    2002-12-19

    lead, arsenic, nickel, mercury and cadmium) is also widespread at the same military facilities due to the use of these metals in ordnance...Eds.), Bioremediation and phytoremediation of chlorinated and recalcitrant compounds. Battelle Second International Conference on Remediation of...Electron Donors, in Wickramanayake, G., Gavashkar, A., Alleman, B., Magar, V., eds. Bioremediation and Phytoremediation of Chlorinated and Recalcitrant

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

    Science.gov (United States)

    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.

  10. Groundwater contamination by chlorinated hydrocarbons in the soil vapour phase - risk assessment at a former dry cleaner site

    Energy Technology Data Exchange (ETDEWEB)

    Danzer, J. [Boden-und-Grundwasser GbR, Sonthofen (Germany)

    2002-07-01

    Chlorinated hydrocarbons, e.g. Perchloroethene (PCE) were commonly used for dry cleaning purposes among other ones. Since they have a significant toxic potential they impose a serious risk to groundwater quality. Due to their physico-chemical properties - particularly high volatility and medium to high water solubility - and their low biodegradation potential they are highly mobile within the unsaturated soil (vapour phase) as well as within the groundwater. This poster (paper) presents data and calculations of a consultant's ''virtual every day'' work in order to assess the risk of groundwater contamination at a former dry cleaner site. (orig.)

  11. Chlorinated polycyclic aromatic hydrocarbons in sediments from industrial areas in Japan and the United States.

    Science.gov (United States)

    Horii, Yuichi; Ohura, Takeshi; Yamashita, Nobuyoshi; Kannan, Kurunthachalam

    2009-11-01

    Chlorinated polycyclic aromatic hydrocarbons (ClPAHs) are widespread environmental pollutants in the urban environment. Nevertheless, there is little information available regarding the occurrence and profiles of ClPAHs in environmental matrices. In this study, residual concentrations and profiles of 20 individual ClPAHs and 16 US EPA-priority PAHs were determined using high- resolution gas chromatography-high-resolution mass spectrometry in sediments from water bodies near industrialized areas: Tokyo Bay, Japan; the Saginaw River watershed, Michigan, USA; a former chlor-alkali plant, Georgia, USA; and the New Bedford Harbor Superfund site, Massachusetts, USA. A sediment core from Tokyo Bay showed temporal patterns in the distribution of ClPAHs from the 1950s through 2004. The fluxes of ClPAHs and 16 priority PAHs in Tokyo Bay sediment core were 0.029-0.57 ng/cm(2)/year and 85-609 ng/cm(2)/year, respectively; fluxes were lowest in the 1950s and highest in 1989-1990. In the United States, a high mean concentration of ClPAHs was found in sediment collected near a former chlor-alkali plant [8820 pg/g dry weight (dry wt)], and lower mean concentrations were found for New Bedford Harbor (1880 pg/g dry wt) and the Saginaw River watershed (1140 pg/g dry wt). Among individual ClPAHs, 6-ClBaP and 1-ClPyr were the dominant compounds in sediments; this pattern is similar to the pattern reported in the literature for waste incineration and ambient urban air samples. Significant correlation between SigmaClPAH concentrations and Sigmaparent-PAH concentrations in Tokyo Bay sediment implies that the sources and distribution of ClPAHs are directly related to those of parent PAHs. We also analyzed ClPAHs and parent PAHs in blue mussels from New Bedford Harbor. The mean concentration of ClPAHs in mussels from New Bedford Harbor was 21 ng/g lipid weight, a concentration three orders of magnitude lower than the mean concentration of parent PAHs. Low-molecular-weight ClPAHs predominated

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

    Science.gov (United States)

    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

  13. The effect of remedial measures upon groundwater quality in connection with soil contamination by chlorinated hydrocarbons and the related costs - by example of the City of Hanover

    International Nuclear Information System (INIS)

    Mull, R.; Mull, J.; Pielke, M.

    1992-01-01

    The effectiveness of remedial actions on the groundwater quality was investigated in the aquifer of the City of Hannover. The improvement of groundwater quality was related to the costs for the remedial actions. The attention was focussed on groundwater pollution by chlorinated hydrocarbons as the most important contaminants of groundwater in urban areas. (orig.)

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

    Science.gov (United States)

    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...

  15. Intrinsic and enhanced bioremediation in aquifers contaminated with chlorinated and aromatic hydrocarbons in The Netherlands

    NARCIS (Netherlands)

    Rijnaarts, H.H.M.; Aalst-van Leeuwen, M.A. van; Heiningen, E. van; Buyzen, H. van; Sinke, A.; Liere, H.C. van; Harkes, M.; Baartmans, R.; Bosma, T.N.P.; Doddema, H.J.

    1998-01-01

    The feasibility of intrinsic and enhanced bioremediation approaches for 16 contaminated sites in the Netherlands are discussed. At at least five out of 10 chlorinated solvent sites, natural attenuation can be used as one of the tools to prevent further dispersion of the plume. At two sites

  16. An investigation into the activation and deactivation of chlorinated hydrocarbons to genotoxins in metabolically competent human cells.

    Science.gov (United States)

    Doherty, A T; Ellard, S; Parry, E M; Parry, J M

    1996-05-01

    We have investigated the induction of micronuclei by 15 chlorinated hydrocarbons in the cytochalasin B-blocked micronucleus assay utilizing genetically engineered cell lines. The human lymphoblastoid cell line AHH-1, with native cytochrome CYP1A1 activity, the MCL-5 cell line, which stably expresses cDNAs encoding human CYP1A2, 2A6, 3A4, 2E1 and microsomal epoxide hydrolase, and the h2E1 cell line, containing a cDNA for CYP2E1, were used in this study. We have demonstrated the induction of kinetochore-positive micronuclei by two chlorinated solvents, 2,3-dichlorobutane and 1,1, 2-trichloroethane, in the metabolically competent cell lines MCL-5 and h2E1. The MCL-5 and h2E1 cell lines have in addition shown the capacity to produce metabolites in the presence of methylene chloride, carbon tetrachloride, 1,2,3-trichloropropane, tetrachloroethylene, toluene and n-hexane, wich yield elevated micronucleus frequencies compared with the parental cell line AHH-1. Hexachloroethane failed to induce micronuclei in any of the cell lines and 1,2-dichloroethane and 1-chlorohexane induced micronuclei without the requirement for metabolic activation in all three cell lines. The MCL-5 cell line exhibited reduced micronucleus frequencies compared with the AHH-1 and h2E1 cell lines following exposure to 1,2-dichloroethylene, 1,3-dichloropropane, 1,1, 1-trichloroethane and 1,2,3-trichloropropane. The methodology used has shown the ability of metabolically competent cell lines expressing cDNAs encoding the cytochrome P450 isoenzymes to metabolize halogenated hydrocarbons to genotoxic species, including both clastogens and aneugens. The biotransformation of chemicals to aneugenic species has not previously been demonstrated.

  17. The use of field redox measurements in assessing remediation of ground water containing petroleum hydrocarbons and chlorinated organic compounds

    International Nuclear Information System (INIS)

    Warner, S.D.; Gallinatti, J.D.; Honniball, J.H.

    1995-01-01

    Field measurements of the reduction-oxidation (redox) condition of ground water were used to assess the effects of in situ remediation of ground water affected by petroleum hydrocarbons and chlorinated organic compounds at multiple sites in northern California. The redox condition of ground water, traditionally measured quickly and inexpensively using a meter that measures electrode potential (Eh), is a valuable parameter by which to assess the conditions that affect the relative stability of various chemicals in ground water. Although not specific to a given redox couple measurements obtained using the traditional Eh meter give a sense of the relative tendency for a ground water to be reducing or oxidizing by providing a measurement of the system Eh. Two cases demonstrate the use of ground water Eh measurements in assessing the effects of in situ ground water remediation. In the first case, ground water affected by petroleum hydrocarbons-gasoline (TPHg), and benzene, toluene, ethylbenzene, and xylenes (BTEX) (ambient Eh of -100 to +100 millivolts [mv]) was treated by injecting hydrogen peroxide to supply oxygen to the subsurface environment and stimulate microbial activity. The second case involved remediation of ground water containing chlorinated organic compounds. In this case, a subsurface permeable ground water treatment wall containing granular iron was installed across the flow path of the affected ground water. The in situ chemical treatment, which successfully dechlorinates compounds such as trichloroethylene, 1,2-dichloroethylene, and vinyl chloride, caused reducing conditions in the ground water, which resulted in the decrease in ground water Eh from am ambient reading of about -50 mv to about -400 mv

  18. Occurrence, profiles, and toxic equivalents of chlorinated and brominated polycyclic aromatic hydrocarbons in E-waste open burning soils.

    Science.gov (United States)

    Nishimura, Chiya; Horii, Yuichi; Tanaka, Shuhei; Asante, Kwadwo Ansong; Ballesteros, Florencio; Viet, Pham Hung; Itai, Takaaki; Takigami, Hidetaka; Tanabe, Shinsuke; Fujimori, Takashi

    2017-06-01

    We conducted this study to assess the occurrence, profiles, and toxicity of chlorinated polycyclic aromatic hydrocarbons (Cl-PAHs) and brominated polycyclic aromatic hydrocarbons (Br-PAHs) in e-waste open burning soils (EOBS). In this study, concentrations of 15 PAHs, 26 Cl-PAHs and 14 Br-PAHs were analyzed in EOBS samples. We found that e-waste open burning is an important emission source of Cl-PAHs and Br-PAHs as well as PAHs. Concentrations of total Cl-PAHs and Br-PAHs in e-waste open burning soil samples ranged from 21 to 2800 ng/g and from 5.8 to 520 ng/g, respectively. Compared with previous studies, the mean of total Cl-PAH concentrations of the EOBS samples in this study was higher than that of electronic shredder waste, that of bottom ash, and comparable to fly ash from waste incinerators in Korea and Japan. The mean of total Br-PAH concentrations of the EOBS samples was generally three to four orders of magnitude higher than those in incinerator bottom ash and comparable to incinerator fly ash, although the number of Br-PAH congeners measured differed among studies. We also found that the Cl-PAH and Br-PAH profiles were similar among all e-waste open burning soil samples but differed from those in waste incinerator fly ash. The profiles and principal component analysis results suggested a unique mechanism of Cl-PAH and Br-PAH formation in EOBS. In addition, the Cl-PAHs and Br-PAHs showed high toxicities equivalent to PCDD/Fs measured in same EOBS samples when calculated based on their relative potencies to benzo[a]pyrene. Along with chlorinated and brominated dioxins and PAHs, Cl-PAHs and Br-PAHs are important environmental pollutants to investigate in EOBS. Copyright © 2016 Elsevier Ltd. All rights reserved.

  19. California sea lions (Zalophus californianus californianus) have lower chlorinated hydrocarbon contents in northern Baja California, Mexico, than in California, USA

    Energy Technology Data Exchange (ETDEWEB)

    Del Toro, Ligeia [Universidad Autonoma de Baja California (UABC), Facultad de Ciencias Marinas, Ensenada, Baja California (Mexico); Investigacion y Conservacion de Mamiferos Marinos de Ensenada, A.C., Placido Mata 2309 Depto. D-5, Condominio Las Fincas, Ensenada, Baja California 22810 (Mexico); Heckel, Gisela [Investigacion y Conservacion de Mamiferos Marinos de Ensenada, A.C., Placido Mata 2309 Depto. D-5, Condominio Las Fincas, Ensenada, Baja California 22810 (Mexico) and Centro de Investigacion Cientifica y de Educacion Superior de Ensenada, B.C. Km 107 Carretera Tijuana-Ensenada, Ensenada, Baja California 22860 (Mexico)]. E-mail: gheckel@cicese.mx; Camacho-Ibar, Victor F. [Instituto de Investigaciones Oceanologicas, UABC, Apdo. Postal 453, Ensenada, Baja California 22860 (Mexico); Schramm, Yolanda [Universidad Autonoma de Baja California (UABC), Facultad de Ciencias Marinas, Ensenada, Baja California (Mexico); Investigacion y Conservacion de Mamiferos Marinos de Ensenada, A.C., Placido Mata 2309 Depto. D-5, Condominio Las Fincas, Ensenada, Baja California 22810 (Mexico)

    2006-07-15

    Chlorinated hydrocarbons (CHs) were determined in blubber samples of 18 California sea lions (Zalophus californianus californianus) that stranded dead along Todos Santos Bay, Ensenada, Baja California, Mexico, January 2000-November 2001. {sigma}DDTs were the dominant group (geometric mean 3.8 {mu}g/g lipid weight), followed by polychlorinated biphenyls ({sigma}PCBs, 2.96 {mu}g/g), chlordanes (0.12 {mu}g/g) and hexachlorocyclohexanes (0.06 {mu}g/g). The {sigma}DDTs/{sigma}PCBs ratio was 1.3. We found CH levels more than one order of magnitude lower than those reported for California sea lion samples collected along the California coast, USA, during the same period as our study. This sharp north-south gradient suggests that Z. californianus stranded in Ensenada (most of them males) would probably have foraged during the summer near rookeries 500-1000 km south of Ensenada and the rest of the year migrate northwards, foraging along the Baja California peninsula, including Ensenada, and probably farther north. - Results suggest that sea lion prey must also have lower hydrocarbons in Baja California than in California in the USA.

  20. California sea lions (Zalophus californianus californianus) have lower chlorinated hydrocarbon contents in northern Baja California, Mexico, than in California, USA

    International Nuclear Information System (INIS)

    Del Toro, Ligeia; Heckel, Gisela; Camacho-Ibar, Victor F.; Schramm, Yolanda

    2006-01-01

    Chlorinated hydrocarbons (CHs) were determined in blubber samples of 18 California sea lions (Zalophus californianus californianus) that stranded dead along Todos Santos Bay, Ensenada, Baja California, Mexico, January 2000-November 2001. ΣDDTs were the dominant group (geometric mean 3.8 μg/g lipid weight), followed by polychlorinated biphenyls (ΣPCBs, 2.96 μg/g), chlordanes (0.12 μg/g) and hexachlorocyclohexanes (0.06 μg/g). The ΣDDTs/ΣPCBs ratio was 1.3. We found CH levels more than one order of magnitude lower than those reported for California sea lion samples collected along the California coast, USA, during the same period as our study. This sharp north-south gradient suggests that Z. californianus stranded in Ensenada (most of them males) would probably have foraged during the summer near rookeries 500-1000 km south of Ensenada and the rest of the year migrate northwards, foraging along the Baja California peninsula, including Ensenada, and probably farther north. - Results suggest that sea lion prey must also have lower hydrocarbons in Baja California than in California in the USA

  1. Impact Of Landfill Closure Designs On Long-Term Natural Attenuation Of Chlorinated Hydrocarbons

    Science.gov (United States)

    2002-03-01

    petroleum hydrocarbons and VC) and to stimulate the precipitation of arsenic (Turpie et al., 2000). Such an engineered remedy provides for continued...precipitation of arsenic . This treatment system provides many advantages over remedial measures currently proposed for this and other similar sites with...1999a. Summary of the Remediation Technologies Development Forum. Phytoremediation Action Team Alternative Cover Assessment Program (ACAP

  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

    Science.gov (United States)

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

    International Nuclear Information System (INIS)

    Umezu, Toyoshi; Shibata, Yasuyuki

    2014-01-01

    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

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

    Energy Technology Data Exchange (ETDEWEB)

    Umezu, Toyoshi, E-mail: umechan2@nies.go.jp; Shibata, Yasuyuki, E-mail: yshibata@nies.go.jp

    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.

  5. Development of a standard reference material containing 22 chlorinated hydrocarbon gases at 1 μmol/mol in nitrogen.

    Science.gov (United States)

    Li, Ning; Du, Jian; Yang, Jing; Fan, Qiang; Tian, Wen

    2017-11-01

    A gas standard mixture containing 22 chlorinated hydrocarbons in high purity nitrogen was prepared using a two-step weighing method and a gasifying apparatus developed in-house. The concentration of each component was determined using a gas chromatograph with flame ionization detection (GC/FID). Linear regression analysis of every component was performed using the gas standard mixture with concentrations ranging from 1 to 10 μmol/mol, showing the complete gasification of volatile organic compound (VOCs) species in a selected cylinder. Repeatability was also examined to ensure the reliability of the preparation method. In addition, no significant difference was observed between domestic treated and imported treated cylinders, which were conducive to reduction of the cost of raw materials. Moreover, the results of stability testing at different pressures and long-term stability tests indicated that the gas standard at 1 μmol/mol level with relative expanded uncertainties of 5% was stable above 2 MPa for a minimum of 12 months. Finally, a quantity comparison was conducted between the gas standard and a commercial gas standard from Scott Specialty Gases (now Air Liquide America Specialty Gases). The excellent agreement of every species suggested the favorable accuracy of our gas standard. Therefore, this reference material can be applied to routine observation of VOCs and for other purposes.

  6. Thermal decomposition of selected chlorinated hydrocarbons during gas combustion in fluidized bed

    Directory of Open Access Journals (Sweden)

    Olek Malgorzata

    2013-01-01

    Full Text Available Abstract Background The process of thermal decomposition of dichloromethane (DCM and chlorobenzene (MCB during the combustion in an inert, bubbling fluidized bed, supported by LPG as auxiliary fuel, have been studied. The concentration profiles of C6H5CI, CH2Cl2, CO2, CO, NOx, COCl2, CHCl3, CH3Cl, C2H2, C6H6, CH4 in the flue gases were specified versus mean bed temperature. Results The role of preheating of gaseous mixture in fluidized bed prior to its ignition inside bubbles was identified as important factor for increase the degree of conversion of DCM and MCB in low bed temperature, in comparison to similar process in the tubular reactor. Conclusions Taking into account possible combustion mechanisms, it was identified that autoignition in bubbles rather than flame propagation between bubbles is needed to achieve complete destruction of DCM and MCB. These condition occurs above 900°C causing the degree of conversion of chlorine compounds of 92-100%.

  7. Treatability of volatile chlorinated hydrocarbon-contaminated soils of different textures along a vertical profile by mechanical soil aeration: A laboratory test.

    Science.gov (United States)

    Ma, Yan; Shi, Yi; Hou, Deyi; Zhang, Xi; Chen, Jiaqi; Wang, Zhifen; Xu, Zhu; Li, Fasheng; Du, Xiaoming

    2017-04-01

    Mechanical soil aeration is a simple, effective, and low-cost soil remediation technology that is suitable for sites contaminated with volatile chlorinated hydrocarbons (VCHs). Conventionally, this technique is used to treat the mixed soil of a site without considering the diversity and treatability of different soils within the site. A laboratory test was conducted to evaluate the effectiveness of mechanical soil aeration for remediating soils of different textures (silty, clayey, and sandy soils) along a vertical profile at an abandoned chloro-alkali chemical site in China. The collected soils were artificially contaminated with chloroform (TCM) and trichloroethylene (TCE). Mechanical soil aeration was effective for remediating VCHs (removal efficiency >98%). The volatilization process was described by an exponential kinetic function. In the early stage of treatment (0-7hr), rapid contaminant volatilization followed a pseudo-first order kinetic model. VCH concentrations decreased to low levels and showed a tailing phenomenon with very slow contaminant release after 8hr. Compared with silty and sandy soils, clayey soil has high organic-matter content, a large specific surface area, a high clay fraction, and a complex pore structure. These characteristics substantially influenced the removal process, making it less efficient, more time consuming, and consequently more expensive. Our findings provide a potential basis for optimizing soil remediation strategy in a cost-effective manner. Copyright © 2016. Published by Elsevier B.V.

  8. Reductive dechlorination of chlorinated hydrocarbons as non-aqueous phase liquid (NAPL): Preliminary investigation on effects of cement doses

    Energy Technology Data Exchange (ETDEWEB)

    Do, Si-Hyun, E-mail: sihyun2@hanyang.ac.kr [Department of Chemical Engineering, Hanyang University, Seoul 133-791 (Korea, Republic of); Batchelor, Bill [Zachry Department of Civil Engineering, Texas A and M University, College Station, TX 77843 (United States)

    2012-07-15

    The reactivities of various types of iron mixtures to degrade chlorinated hydrocarbons (PCE, TCE and 1,1,1-TCA) in the form of non-aqueous phase liquids were investigated. The iron mixtures included a mixture of Fe(II) and Portland cement (Fe(II)-C), a mixture of Fe(II), Fe(III) and Ca(OH){sub 2} (Fe(II/III)-L), and a mixture of Fe(II), Fe(III), Ca(OH){sub 2}, and Portland cement (Fe(II/III)-C). When the same amount of Fe(II) was used, Fe(II)-C was more reactive with chlorinated ethylenes (i.e. PCE and TCE) than Fe(II/III)-L. The reductive pathway for high concentrations of total PCE (i.e. above solubility) with Fe(II)-C was determined to be a combination of two-electron transfer, {beta}-elimination and hydrogenolysis. Increasing the cement dose from 5% to 10% in Fe(II)-C did not affect PCE dechlorination rates, but it did favor the {beta}-elimination pathway. In addition, when Fe(II/III)-C with 5%C was used, PCE dechlorination was similar to that by Fe(II)-C, but this mixture did not effectively degrade TCE. A modified second-order kinetic model was developed and shown to appropriately describe degradation of TCE at high concentrations. Fe(II/III)-L effectively degraded high concentrations of 1,1,1-TCA at rates that were similar to those obtained with Fe(II)-C using 10% C. Moreover, both increasing cement doses and the presence of Fe(III) increased dechlorination rates of 1,1,1-TCA, which was mainly through the hydrogenolysis pathway. The reactivity of Fe(II/III)-L was strongly dependent on the target compound (i.e. less reactivity with TCE, more with 1,1,1-TCA). Therefore, Fe(II/III)-L could be a potential mixture for degrading 1,1,1-TCA, but it should be modified to degrade TCE more effectively. - Highlights: Black-Right-Pointing-Pointer TCE yield indicated that PCE dechlorination was through hydrogenolysis and {beta}-elimination. Black-Right-Pointing-Pointer {beta}-elimination, especially PCE to dichloroacetylene, was favored with the higher cement doses. Black

  9. Comparative evaluation of effects of ozonated and chlorinated thermal discharges on estuarine and freshwater organisms

    Energy Technology Data Exchange (ETDEWEB)

    Guerra, C.R.; Sugam, R.; Meldrim, J.W.; Holmstrom, E.R.; Balog, G.E.

    1980-08-01

    As a part of a program at PSE and G designed to examine the feasibility of ozonation as an alternative to chlorination for control of biofouling in once-through cooling systems, the biological effects of ozonated and chlorinated thermal discharges were evaluated with estuarine and freshwater organisms. Mortality at salinities between 0.5 to 2.5 ppt with mummichog and white perch indicated greater toxicity for chlorine while the alewife, spottail shiner, rainbow trout and white perch in freshwater were more sensitive to ozone. Behavioral and physograhic results were consistent with those observed in toxicity studies. Initial cough response and avoidance concentrations of mummicog and white perch in estuarine waters were lower when exposed to chlorine than to ozone. In freshwater, blueback herring, alewife, rainbow trout, spottail shiner, banded killifish, and white perch avoided lower concentrations of ozone than chlorine.

  10. TiO2 on magnesium silicate monolith: effects of different preparation techniques on the photocatalytic oxidation of chlorinated hydrocarbons

    International Nuclear Information System (INIS)

    Cardona, Ana I.; Candal, Roberto; Sanchez, Benigno; Avila, Pedro; Rebollar, Moises

    2004-01-01

    In this article, the comparative results of the photocatalytic oxidation of trichloroethylene (TCE) alone and a mixture of chlorinated hydrocarbons (trichloroethylene, perchloroethylene and chloroform) in gas phase, obtained with three different monolithic catalysts in a flat reactor frontally illuminated with a Xenon lamp are presented. The three catalysts incorporate titanium dioxide (TiO 2 ) as active phase on a magnesium silicate support, by means of different procedures: (i) incorporation of commercial TiO 2 powder into the silicate matrix ('massic monolith'); (ii) sol-gel coating of the silicate support; (iii) impregnation with a commercial TiO 2 aqueous suspension of the same silicate support. In the first case, the massic monolith was made from a 50:50 w/w mixture of magnesium silicate and 'Titafrance G5' TiO 2 powder. In the second case, a magnesium silicate monolith was coated with several layers of an aqueous TiO 2 sol prepared from hydrolysis and condensation of titanium tetra-isopropoxide (Ti(OC 3 H 7 ) 4 ) in excess of acidified water (acid catalysis). The third catalyst was prepared by impregnating the same silicate support with several layers of 'Titafrance G5' TiO 2 powder water suspension. All the catalysts were thermal treated under comparable conditions in order to fix the TiO 2 active phase to the silicate support. Although the performance of the massic monolith was better than the sol-gel monolith, the latter is of great interest because this technique allows the chemical composition of the active films to be easily modified

  11. Gas-particle phase partitioning and particle size distribution of chlorinated and brominated polycyclic aromatic hydrocarbons in haze.

    Science.gov (United States)

    Jin, Rong; Zheng, Minghui; Yang, Hongbo; Yang, Lili; Wu, Xiaolin; Xu, Yang; Liu, Guorui

    2017-12-01

    Chlorinated and brominated polycyclic aromatic hydrocarbons (Cl/Br-PAHs) are emerging semi-volatile organic pollutants in haze-associated particulate matter (PM). Their gas-particle phase partitioning and distribution among PM fractions have not been clarified. Clarification would increase understanding of atmospheric behavior and health risks of Cl/Br-PAHs. In this study, samples of the gas phase and 4 PM phases (aerodynamic diameters (d ae ) > 10 μm, 2.5-10 μm, 1.0-2.5 μm, and <1.0 μm) were collected simultaneously during haze events in Beijing and analyzed. Normalized histogram distribution indicated that the Cl/Br-PAHs tended to adhere to fine particles. Over 80% of the Cl-PAHs and 70% of the Br-PAHs were associated with fine PM (d ae  < 2.5 μm). The gas-particle phase partitioning and PM distribution of Cl/Br-PAHs when heating of buildings was required, which was associated with haze events, were obviously different from those when heating was not required. The relationship between the logarithmic geometric mean diameters of the Cl/Br-PAH congeners and reciprocal of the temperature (1/T) suggested that low air temperatures during the heating period could lead to high proportions of Cl/Br-PAHs in the fine particles. Increased coal burning during the heating period also contributed to high Cl/Br-PAH loads in the fine particles. Copyright © 2017 Elsevier Ltd. All rights reserved.

  12. Contamination of the eggs of raptors by chlorinated hydrocarbons between 1974 and 1980. [Falco peregrinus, Athene noctua, Falco tinnunculus

    Energy Technology Data Exchange (ETDEWEB)

    Venant, A.; Richou-Bac, L.; Gleizes, E.; Juillard, M.; Terrasse, M.; Terrasse, J.F.

    1984-01-01

    The contents of 206 unfertilized eggs (especially those of birds of prey) were analyzed for residues of chlorinated hydrocarbons (pesticides and PCB) from 1974 to 1980. Eggs collected in Jura (France and Switzerland) were sent deep-frozen to the laboratory. In 1974 and 1975, only 14 peregrine falcon Falco peregrinus eggs were received, and this study therefore really began in 1976. Since 1976, only peregrine falcon, little owl Athene noctua and lesser kestrel Falco tinnunculus eggs have been systematically analyzed. Other results are given for information. No important levels of cyclodienes or BHC were found, but only high levels for HCB, DDE and PCB residues. Of these three species, peregrine falcon eggs were the most contaminated (high level in food chain) but the pollutant levels have seemed to decrease. In 1976, the authors found 1.7 ..mu..g g..pi../sup 1/ HCB, 17.41 ..mu..g g/sup -1/ DDE and 9 ..mu..g g/sup -1/ PCB against 0.269 ..mu..g g/sup -1/ HCB, 5.84 ..mu..g g/sup -1/ DDE and 8.59 ..mu..g g/sup -1/ PCB in 1980 (it is important to record a very high PCB level in 1977 - 63 ..mu..g g/sup -1/. Residue levels were lower for other eggs such as lesser kestrel - 0.029 ..mu..g g/sup -1/ HCB, 0.099 ..mu..g g/sup -1/ DDE, and 0.24 ..mu..g g/sup -1/ PCB; or little owl eggs - 0.041 ..mu..g g/sup -1/ HCB, 1.18 ..mu..g g/sup -1/ DDE, and 0.652 ..mu..g g/sup -1/ PCB in 1980.

  13. Site profiles of low-volatile chlorinated hydrocarbons - cause-oriented monitoring in aquatic media. Vol.2. Low-volatile chlorinated hydrocarbons in surface water, sediments, suspended matter and fish of the Elbe river and its tributaries; Standortprofile schwerfluechtiger chlorierter Kohlenwasserstoffe (SCKW) - ursachenorientiertes Monitoring in aquatischen Medien. Bd. 2. SCKW in Oberflaechenwasser, Sediment, Schwebstoffen und Fischen aus der Elbe und Nebenfluessen

    Energy Technology Data Exchange (ETDEWEB)

    Heinisch, E.; Kettrup, A.; Gebefuegi, I.; Martens, D.; Bergheim, W.; Wenzel, S.

    2001-07-01

    Evaluating the primary data from ARGE ELBE, LAU Halle/Saale and the Environmental Specimen Banking (Umweltprobenbank) as well from publications from the Czech Republic (CHMU) the concentrations of the following low volatile chlorinated hydrocarbons were established for surface water, sediment, breams and eels from the rivers Elbe, Schwarze Elster, Mulde and Saale partly from 1989 till 1999: DDT and its metabolites DDE and DDD, partly as 2,4'- and 4,4' isomers; HCH ({alpha}-, {beta}-, {gamma}- and {delta} isomers); chlorinated benzenes with 1-6 Cl atoms and octachlorostyrene. The data evaluated were drawn up into tables - comprehensive in a separate supplement, in short versions within the text - and consolidated into graphs. Aim of the paper was a cause-oriented monitoring. The by far most important emission sources, found from the distance and time profiles as well as from special assessments of the substance patterns, were chemical plants. (orig.) [German] Durch Auswertung von Primaerdaten der ARGE ELBE, des LAU Halle/Saale und der Umweltprobenbank sowie von Publikationen aus Tschechien (CHMU) wurden fuer Oberflaechenwasser, Sediment, Brassen/Bleien und Aale aus der Elbe, Schwarzen Elster, Mulde und Saale fuer die Jahre von z.T. 1989 bis 1999 die Konzentrationen der folgenden schwerfluechtigen Kohlenwasserstoffe (SCKW) ermittelt: DDT und seine Metabolite DDE und DDD, z.T. als 2,4'- und 4,4'-Isomere; HCH ({alpha}-, {beta}-, {gamma}- und {delta}-Isomere); chlorierte Benzole mit 1-6 Cl-Atomen und Octachlorstyrol. Die ausgewerteten Daten wurden zu Tabellen - ausfuehrlich in einem gesonderten Tabellenanhang und verkuerzt im Textteil - zusammengestellt sowie zu Grafiken verdichtet. Ziel der Arbeit war ein ursachenorientiertes Monitoring. Als mit Abstand wesentlichste Emissionsquellen konnten anhand von Streckenprofilen und Zeitrastern sowie durch spezielle Auswertungen der Stoffmusterverteilungen Chemibetriebe ermittelt werden. (orig.)

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

    Science.gov (United States)

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

    2015-12-01

    Tramadol (TRA) is one of the most detected analgesics in environmental matrices, and it is of high significance to study the reactivity of TRA during chlorination considering its potential toxicity to the environment. The chlorine/TRA reaction is first order with respect to the TRA concentration, and a combination of first-order and second-order with respect to chlorine concentration. The pH dependence of the observed rate constants (kobs) showed that the TRA oxidation reactivity increased with increasing pH. kobs can be quantitatively described by considering all active species including Cl2, Cl2O and HOCl, and the individual rate constants of HOCl/TRA(0), HOCl/TRAH(+), Cl2/TRA and Cl2O/TRA reactions were calculated to be (2.61±0.29)×10(3)M(-1)s(-1), 14.73±4.17M(-1)s(-1), (3.93±0.34)×10(5)M(-1)s(-1) and (5.66±1.83)×10(6)M(-1)s(-1), respectively. Eleven degradation products were detected with UPLC-Q-TOF-MS, and the corresponding structures of eight products found under various pH conditions were proposed. The amine group was proposed to be the initial attack site under alkaline pH conditions, where reaction of the deprotonated amine group with HOCl is favorable. Under acidic and neutral pH conditions, however, two possible reaction pathways were proposed. One is an electrophilic substitution on the aromatic ring, and another is an electrophilic substitution on the nitrogen, leading to an N-chlorinated intermediate, which can be further oxidized. Finally, the SOS/umu test showed that the genotoxicity of TRA chlorination products increased with increasing dosage of chlorine, which was mostly attributed to the formation of some chlorine substitution products. Copyright © 2015 Elsevier Ltd. All rights reserved.

  15. Occurrence and distribution of persistent chlorinated hydrocarbons in the seas around India

    Digital Repository Service at National Institute of Oceanography (India)

    Sarkar, A.

    Article deals with an evaluation of the levels of contamination of various organochlorine pesticides such as DDTs, HCHs, aldrin, dieldrin, endrin, and different congeners of polychlorinated biphenyls in different compartment of the ocean (water...

  16. Evaluation of hydrocarbon potential, Task 8

    International Nuclear Information System (INIS)

    Cashman, P.H.; Trexler, J.H. Jr.

    1993-01-01

    Task 8 is responsible for assessing the hydrocarbon potential of the Yucca Mountain vicinity. Our main focus is source rock stratigraphy in the Nevada Test Site (NTS) area in southern Nevada. In order to reconstruct the Paleozoic stratigraphy, we are also studying the geometry and kinematics of deformation at NTS. A thorough understanding of the structure will also be essential to predicting the nature of the Late Paleozoic rocks under Yucca Mountain. Our stratigraphic studies continue to support the interpretation that rocks mapped as the open-quotes Eleana Formationclose quotes are in fact parts of two different Mississippian units. We are now provisionally limiting the name open-quotes Eleana Formationclose quotes to the rocks that make up the Eleana Range - i.e., the rocks that we have been calling open-quotes western Eleanaclose quotes. The mudstone section (which we have until now called open-quotes eastern Eleanaclose quotes) we are provisionally calling the open-quotes Chainman Shaleclose quotes, in keeping with regional lithostratigraphic nomenclature. We continue to work out the internal stratigraphies and basin histories of both units; XRD (r-ray diffraction) determinations of clay mineralogy are an addition to our understanding of the Chainman. The basin histories place important constraints on regional paleogeographic and tectonic reconstructions. This year we have hired a consulting petroleum geologist for two jobs: (1) to review drillhole data from southern Nevada on file at NBMG and make recommendations about more detailed study of any interesting drillholes; and (2) to log the UE17e core (in the Chainman) and evaluate source rock potential. The results of these studies have been incorporated into this report, and the consultant's reports

  17. EVALUATION OF PETROLEUM HYDROCARBONS ELUTION FROM SOIL

    Directory of Open Access Journals (Sweden)

    Janina Piekutin

    2015-06-01

    Full Text Available The paper presents studies on oil removal from soil by means of water elution with a help of shaking out the contaminants from the soil. The tests were performed on simulated soil samples contaminated with a mixture of petroleum hydrocarbons. The study consisted in recording the time influence and the number of elution cycles to remove contaminants from the soil. The samples were then subject to the determination of petroleum hydrocarbons, aliphatic hydrocarbons, and BTEX compounds (benzene, toluene, ethylbenzene, xylene. Due to adding various concentrations of petroleum into particular soil samples and applying different shaking times, it was possible to find out the impact of petroleum content and sample shaking duration on the course and possibility of petroleum substances removal by means of elution process.

  18. Evaluation of Hydrocarbons Level and Identification of Indigenous ...

    African Journals Online (AJOL)

    PROF HORSFALL

    Auto-Mechanic Workshops along Ikokwu Mechanic Village, Port Harcourt, Nigeria. *1AKOMAH, ON .... The study was aimed at evaluating the levels of hydrocarbon and ..... tropical countries, Cambridge University Press. United Kingdom 2: ...

  19. Reversed phase liquid chromatography with UV absorbance and flame ionization detection using a water mobile phase and a cyano propyl stationary phase Analysis of alcohols and chlorinated hydrocarbons.

    Science.gov (United States)

    Quigley, W W; Ecker, S T; Vahey, P G; Synovec, R E

    1999-10-01

    The development of liquid chromatography with a commercially available cyano propyl stationary phase and a 100% water mobile phase is reported. Separations were performed at ambient temperature, simplifying instrumental requirements. Excellent separation efficiency using a water mobile phase was achieved, for example N=18 800, or 75 200 m(-1), was obtained for resorcinol, at a retention factor of k'=4.88 (retention time of 9.55 min at 1 ml min(-1) for a 25 cmx4.6 mm i.d. column, packed with 5 mum diameter particles with the cyano propyl stationary phase). A separation via reversed phase liquid chromatography (RP-LC) with a 100% water mobile phase of six phenols and related compounds was compared to a separation of the same compounds by traditional RP-LC, using octadecylsilane (ODS), i.e. C18, bound to silica and an aqueous mobile phase modified with acetonitrile. Nearly identical analysis time was achieved for the separation of six phenols and related compounds using the cyano propyl stationary phase with a 100% water mobile phase, as compared to traditional RP-LC requiring a relatively large fraction of organic solvent modifier in the mobile phase (25% acetonitrile:75% water). Additional understanding of the retention mechanism with the 100% water mobile phase was obtained by relating measured retention factors of aliphatic alcohols, phenols and related compounds, and chlorinated hydrocarbons to their octanol:water partition coefficients. The retention mechanism is found to be consistent with a RP-LC mechanism coupled with an additional retention effect due to residual hydroxyl groups on the cyano propyl stationary phase. Advantages due to a 100% water mobile phase for the chemical analysis of alcohol mixtures and chlorinated hydrocarbons are reported. By placing an absorbance detector in-series and preceding a novel drop interface to a flame ionization detector (FID), selective detection of a separated mixture of phenols and related compounds and aliphatic

  20. Application of BGPR tomography investigate the Soil and Groundwater Contaminated with Chlorinated Hydrocarbon:Case study

    Science.gov (United States)

    Liu, H. C.; Lin, C. P.; Dong, T. H.; Yang, C. H.

    2014-12-01

    The success of an environmental contaminated project is often determined by the extent to which it is able to ascertain and control subsurface conditions. At present, site managers have limited tools to gain detailed information on the distribution of possible underground barriers or anomalous bodies. The technology employed in Taiwan to evaluate or confirm subsurface anomalies relies primarily on surface geophysical surveys, borehole drillings, or past records. Surface ground-penetrating radar GPR survey is among the most popular of these methods. Surface GPR technique can be used in many ways, but this method is not always the best suited to Taiwan's conditions. Surface GPR surveys are adversely affected by the conductivity of silty/clayey sediment and cultural noises. As a result, when surface GPR surveys are used, both detection and resolution of subsurface anomalies will decrease with depth. In order to overcome these obstacles, the use of borehole GPR BGPR with a few boreholes may provide a more direct and effective way to detect an underground target. Recent improvement in the quality of BGPR contributes to the suitability of this type of survey work when implemented on construction sites. This paper ues the BGPR geophysical technology has been developed to overcome above limitations. The information of multi-wells logging could be used to interpret the permeability of subsurface, the dominate flow path and the hot-spot for evaluating the distribution of pollution and the efficiency of remediation in different time sequences.

  1. Penetrometer compatible, fiber-optic sensor for continuous monitoring of chlorinated hydrocarbons -- field test results

    International Nuclear Information System (INIS)

    Milanovich, F.P.; Brown, S.B.; Colston, B.W. Jr.

    1993-04-01

    We have developed and field tested a fiber optic chemical sensor for use in environmental monitoring and remediation. The principle of detection is colorimetric and is based on an irreversible chemical reaction between a specific reagent and the target compound. The formation of reaction products are monitored remotely with optical fibers. Successive or on-demand measurements are made possible with a reagent reservoir and a miniature pumping system. The sensor has been evaluated against gas chromatography standards and has demonstrated accuracy and sensitivity (>5ppb w/w) sufficient for the environmental monitoring of the contaminants triceoroethlyene (TCE) and chloroform. The sensor system can be used for bench-top analyses or for in-situ measurements such as groundwater and vadose monitoring wells or in Penetrometry mediated placements

  2. Task 8: Evaluation of hydrocarbon potential

    International Nuclear Information System (INIS)

    Cashman, P.H.; Trexler, J.H. Jr.

    1994-01-01

    Our studies focus on the stratigraphy of Late Devonian to early Pennsylvanian rocks at the NTS, because these are the best potential hydrocarbon source rocks in the vicinity of Yucca Mountain. In the last year, our stratigraphic studies have broadened to include the regional context for both the Chainman and the Eleana formations. New age data based on biostratigraphy constrain the age ranges of both Chainman and Eleana; accurate and reliable ages are essential for regional correlation and for regional paleogeographic reconstructions. Source rock analyses throughout the Chainman establish whether these rocks contained adequate organic material to generate hydrocarbons. Maturation analyses of samples from the Chainman determine whether the temperature history has been suitable for the generation of liquid hydrocarbons. Structural studies are aimed at defining the deformation histories and present position of the different packages of Devonian - Pennsylvanian rocks. This report summarizes new results of our structural, stratigraphic and hydrocarbon source rock potential studies at the Nevada Test Site and vicinity. Stratigraphy is considered first, with the Chainman Shale and Eleana Formation discussed separately. New biostratigraphic results are included in this section. New results from our structural studies are summarized next, followed by source rock and maturation analyses of the Chainman Shale. Directions for future work are included where appropriate

  3. Contamination of Omnivorous Freshwater Fish Species and Sediments by Chlorinated Hydrocarbons in Poland

    Directory of Open Access Journals (Sweden)

    Niewiadowska Alicja

    2014-10-01

    Full Text Available The occurrence and concentrations of organochlorine pesticides and polychlorinated biphenyls (PCBs were determined in 158 muscle samples of bream (Abramis brama and roach (Rutilus rutilus, and 84 samples of sediments collected from 10 river and lake sampling sites in 2011 and 2012. The concentrations of DDTs (p,p’-DDT, o,p’-DDT, p,p’-DDE, and p,p’-DDD, HCH isomers (a-, ß-, and y-HCH, HCB, and PCBs (six indicator PCB congeners 28, 52, 101, 138, 153 and 180 were determined using the capillary gas chromatography. The mean concentrations of DDTs in bream and roach were in the range of 11.2-654 and 4.5-121 ug/kg wet weight respectively, and PCBs were in the range of 1.3-75.9 and 1.1-112 ug/kg wet weight, respectively. Mean concentrations of DDTs and PCBs in sediments were 0.5-270 ug/kg dry weight and ⋋0.1-2.2 ug/kg dry weight respectively. The study showed clear spatial differences in the levels of organochlorine pesticides and PCBs in fish and sediments from different aquatic ecosystems. The highest levels of contaminants were detected in fish and sediments from the Vistula River in vicinity of Cracow. The possible risk to the fish meat consumers and ecological risk were evaluated.

  4. Intercalibration of analytical methods on marine environmental samples. Results of MEDPOL-II exercise for the intercalibration of chlorinated hydrocarbon measurements on mussel homogenate (MA-M-2/OC)

    International Nuclear Information System (INIS)

    1986-10-01

    Mussels have been considered as good indicators of chlorinated hydrocarbon pollution of the marine environment and this led to the development of mussel watch programmes in many countries in the late seventies. These intercalibration exercises were arranged in order to increase the quality of analytical capabilities of environmental laboratories. The samples MA-M-2/0C of Mediterranean mussels with chlorinated hydrocarbon content were checked by 27 laboratories. It was judged highly suitable for these laboratories to have at their disposal a reference material made of mussel tissue with robust estimations of the true values with respect to several chlorinated hydrocarbons. Such a material would allow chemists to check the validity of new analytical procedures

  5. Persistent chlorinated hydrocarbons and mercury in birds caught off the west coast of Spitsbergen. [Larus hyperboreus, Fulmarus glacialis, Uria lomvia, Alle alle, Somateria mollissima

    Energy Technology Data Exchange (ETDEWEB)

    Norheim, G.; Kjos-Hanssen, B.

    1984-01-01

    The tissue concentrations of DDE, PCB, hexachlorobenzene (HCB) and mercury were determined in five species of migrating seabirds: glaucous gull Larus hyperboreus; fulmar Fulmarus glacialis; Bruennech's guillemot Uria lomvia; little auk Alle alle and eider Somateria mollissima. These birds nest on Svalbard and were shot in May 1980 off the west coast of Spitsbergen. The highest levels of DDE, PCB and HCB were found in glaucous gull, whilst low levels were found in Bruennich's guillemot, little auk and, expecially, eider. Fulmars were intermediate. Highly significant correlations were found between the concentrations of HCB, DDE and PCB. These results could indicate that the Gulf Stream is a common source of these substances. The highest mercury levels were found in the fulmar; glaucous gull and eider were intermediate, whilst the lowest mercury levels were found in Bruennich's guillemot and little auk. There was no connection between the nutritional condition and concentrations of the pollutants determined. However, there seems to be a close relationship between the levels of chlorinated hydrocarbons and the trophic level of the birds in the food chain. A comparison between the present results and analyses of Antartic seabirds indicates that the aquatic food chain in the Arctic is more loaded with persistent chlorinated hydrocarbons than in the Antarctic, whereas more mercury seems to be found in Antarctic birds.

  6. Development and evaluation of analytical techniques for total chlorine in burner fuels

    International Nuclear Information System (INIS)

    Gaskill, A. Jr.; Estes, E.D.; Hardison, D.L.; Friedman, P.H.

    1987-01-01

    A current EPA regulation prohibits the sale for burning in non-industrial boilers of used oils and oil fuels contaminated above specified levels with certain metals and total chlorine. When burned as fuel in a small boiler, the contaminants may be emitted to the ambient air at hazardous levels. This regulation establishes a rebuttable presumption that used oil containing more than 1,000 ppm total chlorine has been mixed with halogenated solvents and is a hazardous waste. Rebutting the presumption requires the seller of the oil to prove that this chlorine is not due to halogenated solvents or other hazardous halogenated organics. If the rebuttal is successful, the oil can be sold as fuel up to a level of 4000 ppm total chlorine. Analytical techniques for determination of total chlorine were evaluated or developed to provide regulatory agencies and the regulated community with appropriate chlorine test methods. The techniques evaluated included chemical titrations following oxygen bomb combustion, disposable field test kits, instrumental microcoulometry, and x-ray fluorescence spectrometry. These candidate techniques were subjected to interlaboratory testing to estimate their precision, accuracy, sensitivity, and susceptibility to matrix effects. Information on ease of use and analysis costs was also collected. Based on this pilot study, test methods will be written for the most promising techniques and subjected to a formal collaborative study to generate precision and accuracy data for each method. These methods are to be proposed in the Federal Register as mandatory for compliance with the existing used oil regulation

  7. Development and evaluation of analytical techniques for total chlorine in used oils and oil fuels

    International Nuclear Information System (INIS)

    Gaskill, A. Jr.; Estes, E.D.; Hardison, D.L.; Friedman, P.H.

    1990-01-01

    A current EPA regulation prohibits the sale for burning in nonindustrial boilers of used oils and oil fuels. This paper discusses how analytical techniques for determining total chlorine were evaluated to provide regulatory agencies and the regulated community with appropriate chlorine test methods. The techniques evaluated included oxygen bomb combustion followed by chemical titration or ion chromatography, instrumental microcoulometry, field test kits, and instrumental furnace/specific ion electrode determinator, a device based on the Beilstein reaction, and x-ray fluorescence spectrometry. These techniques were subjected to interlaboratory testing to estimate their precision, accuracy, and sensitivity. Virgin and used crankcase oils, hydraulic and metalworking oils, oil fuels and oil fuel blends with used oils were tested. The bomb techniques, one of the test kits, microcoulometry and all but one x-ray analyzer were found to be suitable for this application. The chlorine furnace and the Beilstein device were found to be inapplicable at the levels of interest

  8. Evaluation of hydrocarbons level and identification of indigenous ...

    African Journals Online (AJOL)

    Evaluation of hydrocarbons level and identification of indigenous bacteria in soil from auto-mechanic workshops along Ikokwu Mechanic Village, Port Harcourt, ... (ii) it is essential that the metagenomics of spent engine oil contaminated soil at auto-mechanic workshop be studied for optimum utilization of their potentials.

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

    Science.gov (United States)

    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

  10. Hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    1927-02-22

    Coal tar, mineral oils, bitumens, coal extraction products, hydrogenation products of coal, oil schists can be atomized and heated with steam to decompose pyrogenetically and form gases rich in olefins which may be heated with or without pressure and with or without catalysts to produce liquid hydrocarbons of low boiling point, some of which may be aromatic. The apparatus should be lined with copper, silica, or ferrosilicon to prevent contact of the bases with iron which causes deposition of soot. Catalysts used may be metal oxides, silica, graphite, active charcoal, mica, pumice, porcelain, barium carbonate, copper, silver, gold, chromium, boron, or their compounds. At temperatures from 300 to 400/sup 0/C, olefins are produced. At higher temperatures, naphthenes and benzene hydrocarbons are produced.

  11. Evaluation of possible use of disinfectant based on chlorine dioxide in dairy plant

    Directory of Open Access Journals (Sweden)

    Rakić-Martinez Mira

    2009-01-01

    Full Text Available Poor sanitation of food contact surfaces has been a contributing factor in food borne disease outbreaks, especially those involving Listeria monocytogenes, Salmonella spp., Escherichia coli, Staphylococcus aureus etc. The objectives of this study were therefore to: 1. Determine the efficiency of a disinfectant based on chlorine dioxide in suspension in a closed system in a dairy plant. 2. Evaluate the possibility of disinfection of working surfaces with a disinfectant based on chlorine dioxide. In order to determine the germicidal effect of the disinfectant based on chlorine dioxide by suspension test (BSEN 1276:1997; the following test organisms were used: Listeria monocytogenes, Proteus mirabilis, Escherichia coli, Bacillus cereus, Staphylococcus aureus and Pseudomonas aeruginosa clinical isolate. The corrosive properties of the disinfectant based on chlorine dioxide were tested by IDF 077:1977 standard. The efficacy of this disinfectant was investigated in a closed system in a dairy plant. Results indicated a 100% reduction of >108 cfu/ml L. monocytogenes, E. coli, Proteus mirabilis, Pseudomonas aeruginosa, S. aureus, viable count after 1 minute of exposure to 100 ppm of the disinfectant based on chlorine dioxide and 400 ppm for Bacillus cereus. In the presence of 2% skim milk and 4 % skim milk concentrations of 200 and 250 ppm resulted in 100% reduction in numbers of the five of six test microorganisms, respectively. The spore former, Bacillus cereus is less susceptible to the disinfectant. Therefore, the efficient concentration for 100% reduction in viable count after 1 minute exposure was 500 ppm. The corrosive properties of the disinfectant were not determined. In the case of closed system disinfection in a dairy plant, reduction in viable count after 15 minute exposure to 100 ppm of disinfectant based on chlorine dioxide ranged from 80 to 100%.

  12. Evaluation on joint toxicity of chlorinated anilines and cadmium to Photobacterium phosphoreum and QSAR analysis

    Energy Technology Data Exchange (ETDEWEB)

    Jin, Hao, E-mail: realking163@163.com [School of Life and Chemistry, Jiangsu Second Normal University, Nanjing, Jiangsu 210013 (China); Wang, Chao; Shi, Jiaqi [State Key Laboratory of Pollution Control and Resources Reuse, School of Environment, Nanjing University, Nanjing, Jiangsu 210023 (China); Chen, Lei [School of Life and Chemistry, Jiangsu Second Normal University, Nanjing, Jiangsu 210013 (China)

    2014-08-30

    Highlights: • Cd has different effects on joint toxicity when in different concentrations. • The toxicity of most binary mixtures decreases when Cd concentration rises. • Different QSAR models are developed to predict the joint toxicity. • Descriptors in QSARs can help to elucidate the joint toxicity mechanism. • Van der Waals’ force or complexation may reduce the toxicity of mixtures. - Abstract: The individual IC{sub 50} (the concentrations causing a 50% inhibition of bioluminescence after 15 min exposure) of cadmium ion (Cd) and nine chlorinated anilines to Photobacterium phosphoreum (P. phosphoreum) were determined. In order to evaluate the combined effects of the nine chlorinated anilines and Cd, the toxicities of chlorinated anilines combined with different concentrations of Cd were determined, respectively. The results showed that the number of chlorinated anilines manifesting synergy with Cd decreased with the increasing Cd concentration, and the number manifesting antagonism decreased firstly and then increased. The joint toxicity of mixtures at low Cd concentration was weaker than that of most binary mixtures when combined with Cd at medium and high concentrations as indicated by TU{sub Total}. QSAR analysis showed that the single toxicity of chlorinated anilines was related to the energy of the lowest unoccupied molecular orbital (E{sub LUMO}). When combined with different concentrations of Cd, the toxicity was related to the energy difference (E{sub HOMO} − E{sub LUMO}) with different coefficients. Van der Waals’ force or the complexation between chlorinated anilines and Cd had an impact on the toxicity of combined systems, which could account for QSAR models with different physico-chemical descriptors.

  13. Migration of chlorinated hydrocarbons in multilayer unconsolidated porous media: a case study from the Po Plain, Italy

    Directory of Open Access Journals (Sweden)

    Maria Filippini

    2017-12-01

    Full Text Available Chlorinated solvents are the most ubiquitous organic contaminants found in groundwater since the last six decades. Due to their high degree of carcinogenicity/toxicity and the relatively high mobility and persistence, they represent a serious threat against the human health and the environment. These contaminants generally reach groundwater as Dense Non-Aqueous Phase Liquid (DNAPL that can migrate through aquifers easier than aqueous contaminants. The complex phase partitioning to which chlorinated solvent DNAPLs can undergo (i.e. to the dissolved, vapor or sorbed phase, as well as their transformations (e.g. degradation, depend on the physico-chemical properties of the contaminants and on the features of the hydrogeological system in which they migrate. The hydrogeologic setting below the city of Ferrara (Po plain, northern Italy, which is affected by scattered contamination by chlorinated solvents, has been investigated. In particular, a limited-inspace high-resolution investigation was performed in one selected contaminated test-site, known as “Caretti site”. Here, high-resolution vertical profiling of different kind of data (i.e. stratigraphic data, hydraulic heads, hydrochemical composition of water, stable isotopes of water and contaminants were collected by means of multilevel monitoring systems and other innovative sampling and analytical techniques. The main goals of the research were to assess the intrinsic vulnerability of the aquifers and to identify the dynamics of migration and transformation of the chloroethene contaminants in relationship to the features of the hosting porous medium. The confined aquifers turned out to be more vulnerable to DNAPLs than aqueous contaminants due to the occurrence of microfractures in the overlying clayey aquitards. The presence of organic-rich deposits in the local stratigraphy enhanced the biodegradation of chloroethenes causing accumulation of Vinyl Chloride. The results are useful at the

  14. Comparative analysis of concentrations of lead, cadmium and mercury in cord blood, maternal blood, and breast milk, as well as persistent chlorinated hydrocarbons in maternal milk samples from Germany and Iran

    International Nuclear Information System (INIS)

    Javanmardi, F.

    2001-01-01

    The concentration of the heavy metals lead, cadmium and mercury in cord blood, maternal blood and breast milk has been studied. Lead and cadmium were analyzed by atomic absorption spectrometry. Mercury was determined using the flow-injection hydride technique. According to the concentrations of heavy metals and chlorinated hydrocarbons we ascertained for the region of Rendsburg, the toxic risk for infants relative to the consumption of contaminated maternal milk can be viewed as very slight. (orig.) [de

  15. Evaluation of Chlorine Treatment Levels for Inactivation of Human Norovirus and MS2 Bacteriophage during Sewage Treatment.

    Science.gov (United States)

    Kingsley, David H; Fay, Johnna P; Calci, Kevin; Pouillot, Régis; Woods, Jacquelina; Chen, Haiqiang; Niemira, Brendan A; Van Doren, Jane M

    2017-12-01

    This study examined the inactivation of human norovirus (HuNoV) GI.1 and GII.4 by chlorine under conditions mimicking sewage treatment. Using a porcine gastric mucin-magnetic bead (PGM-MB) assay, no statistically significant loss in HuNoV binding (inactivation) was observed for secondary effluent treatments of ≤25 ppm total chlorine; for both strains, 50 and 100 ppm treatments resulted in ≤0.8-log 10 unit and ≥3.9-log 10 unit reductions, respectively. Treatments of 10, 25, 50, and 100 ppm chlorine inactivated 0.31, 1.35, >5, and >5 log 10 units, respectively, of the norovirus indicator MS2 bacteriophage. Evaluation of treatment time indicated that the vast majority of MS2 and HuNoV inactivation occurred in the first 5 min for 0.2-μm-filtered, prechlorinated secondary effluent. Free chlorine measurements of secondary effluent seeded with MS2 and HuNoV demonstrated substantial oxidative burdens. With 25, 50, and 100 ppm treatments, free chlorine levels after 5 min of exposure ranged from 0.21 to 0.58 ppm, from 0.28 to 16.7 ppm, and from 11.6 to 53 ppm, respectively. At chlorine treatment levels of >50 ppm, statistically significant differences were observed between reductions for PGM-MB-bound HuNoV (potentially infectious) particles and those for unbound (noninfectious) HuNoV particles or total norovirus particles. While results suggested that MS2 and HuNoV (measured as PGM-MB binding) behave similarly, although not identically, both have limited susceptibility to chlorine treatments of ≤25 ppm total chlorine. Since sewage treatment is performed at ≤25 ppm total chlorine, targeting free chlorine levels of 0.5 to 1.0 ppm, these results suggest that traditional chlorine-based sewage treatment does not inactivate HuNoV efficiently. IMPORTANCE HuNoV is ubiquitous in sewage. A receptor binding assay was used to assess inactivation of HuNoV by chlorine-based sewage treatment, given that the virus cannot be routinely propagated in vitro Results reported here

  16. Persistent chlorinated hydrocarbons (PHC) - end products and intermediate products of technical synthesis processes in surface water of the Rhine region. Vol. 5: Site profiles of persistent chlorinated hydrocarbons - source-oriented monitoring in aquatic media; Persistente chlorierte Kohlenwasserstoffe (PCKW) - End- und Zwischenprodukte technischer Synthesen in Gewaessern der Rheinregion. Band 5 der Reihe: Standortprofile persistenter chlorierter Kohlenwasserstoffe - ursachenorientiertes Monitoring in aquatischen Medien

    Energy Technology Data Exchange (ETDEWEB)

    Heinisch, E.; Kettrup, A.; Bergheim, W.; Wenzel, S.

    2003-07-01

    By evaluating the primary data from 20 regional institutions in the period 1984-2002 about persistent chlorinated hydrocarbons (PCHC) in fishes (eels, Anguilla anguilla; breams, Abramis brama; barbs, Barbus barbus and reaches, Rutilus rutilus), sediment and suspended matter it was tried to mark the burdens and substance profiles for sampling sites on the river Rhine and rivers in BW, Hess, RP and NRW. The compounds investigated were the isomere di-, tri- and tetrachlorobenzenes, penta- and hexachlorobenzene, octachlorostyrene (OCS), hexachlorobutadiene (HCBD) as well as the 6 DIN (IUPAC, Ballschmiter) congeners of the PCB, substances which were - as to the REACH - described as PBT, partly as vPvB substances and regarded as ''priority harmful substances'' (PCBz; HCB, HCBD), respectively. The statistically elaborated single data were summarized in distance profiles and time series, aiming at marking local and regional immissions as well as hints to their origin and current importance. The background of these efforts is the lack of specialized publications about technical synthesis or compulsory yield of the compounds concerning kind, amount and period. Especially tetrachlorobenzene (mainly 1,2,4,5-TeCBz) and HCBD could be defined as indicator substances for past and recent technical synthesis of chloroorganic compounds. The higher chlorinated PCB congeners no. 138, 153 and 180 (HPCB) proved very persistent. The sites of chemical industry in the vicinity of the sampling points Rheinfelden, Grenzach, Lampertheimer Altrhein, Biebesheimer Rhein, Muendung Schwarzbach, Bischofsheim and Griesheim (Main), Hitdorf, Duisburg-Homberg und Huels (Lippe) could be made transparent by maxima and special substance patterns. (orig.) [German] Durch Auswertung von Primaerdaten ueber persistente chlorierte Kohlenwasserstoffe (PCKW) in Fischen (Aale, Anguilla anguilla; Brachsen, Abramis brama; Barben, Barbus barbus und Rotaugen, Rutilus rutilus), Sediment und

  17. Application of chemical tools to evaluate phytoremediation of weathered hydrocarbons

    International Nuclear Information System (INIS)

    Camp, H.; Kulakow, P.; Smart, D.R.; O'Reilly, K.

    2002-01-01

    The effectiveness of using phytoremediation methods to treat soils contaminated with hydrocarbons was tested in a three-year study at a site in northern California at a treatment pond for refinery process water. The treatment pond was drained several years ago and is targeted for cleanup. The petroleum hydrocarbons from the refinery waste were already highly degraded from natural weathering processes by the time the study began. The soil consists of about 23 per cent sand, 38 per cent silt, and 39 per cent clay. The study followed the Environmental Protection Agency's standardized field protocol and analytical approach. During the study, chemical data for several hydrocarbon parameters was gathered. Soil samples were Soxhlet-extracted in organic solvent and measured for oil and grease and total petroleum hydrocarbons using gravimetric techniques. One of the objectives was to develop an accurate quantitative way to identify sites and conditions where phytoremediation will be effective to supplement decision-tree-type approaches. The focus of the study is the application of chemical data in evaluating the effectiveness of the treatment process. Phytoremediation uses living plants for in situ remediation of polluted soils. The basic benefits of the techniques is that it is aesthetically pleasing, natural and passive. In addition, it is effective in cleaning up sites with low to moderate levels of pollution at shallow depths. A particular form of phytoremediation called rhizodegradation or enhanced rhizosphere biodegradation was the treatment used in this study. It is a treatment in which microorganisms digest organic substances and beak them down by biodegradation while being supported in the plant root structure. Test results indicate that the effects of phytoremediation treatments are subtle for highly weathered source material. It was noted that more statistical analysis will be performed with the data to determine compositional changes due to phytoremediation

  18. Electrical resistivity and induced polarization tomography in identifying the plume of chlorinated hydrocarbons in sedimentary formation: a case study in Rho (Milan - Italy).

    Science.gov (United States)

    Cardarelli, Ettore; Di Filippo, Gerardina

    2009-09-01

    Resistivity and induced polarization surveying were originally developed for mineral exploration but are now finding new applications in the field of environmental and engineering geophysics. The present article reports the results of a geophysical survey performed with the aim of identifying a plume of chlorinated hydrocarbons in sedimentary formations of the Pandania plain. The tested site is characterized by three sand and gravel aquifers containing a quantity of clay particles which influence the overall bulk resistivity and chargeability. According to data obtained using shallow boreholes, mainly dense non-aqueous phase liquids were found as contaminants in the first and second aquifer. The aforementioned geo-electrical methods were applied in both two- and three-dimensional approaches. Steel and copper electrodes were used in the process of field data acquisition and the results of the survey were compared. The geophysical survey revealed some anomalies that could be explained by the presence of dense non-aqueous phase liquids in the soil medium. The concept of normalized chargeability facilitates the interpretation of detected induced polarization anomalies. The shape of the plume was inferred from maps of resistivity and chargeability to a depth of 25 m below the surface of the ground.

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

    Science.gov (United States)

    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. Copyright © 2014 Elsevier Ltd. All rights reserved.

  20. Quicklime-induced changes of soil properties: Implications for enhanced remediation of volatile chlorinated hydrocarbon contaminated soils via mechanical soil aeration.

    Science.gov (United States)

    Ma, Yan; Dong, Binbin; He, Xiaosong; Shi, Yi; Xu, Mingyue; He, Xuwen; Du, Xiaoming; Li, Fasheng

    2017-04-01

    Mechanical soil aeration is used for soil remediation at sites contaminated by volatile organic compounds. However, the effectiveness of the method is limited by low soil temperature, high soil moisture, and high soil viscosity. Combined with mechanical soil aeration, quicklime has a practical application value related to reinforcement remediation and to its action in the remediation of soil contaminated with volatile organic compounds. In this study, the target pollutant was trichloroethylene, which is a volatile chlorinated hydrocarbon pollutant commonly found in contaminated soils. A restoration experiment was carried out, using a set of mechanical soil-aeration simulation tests, by adding quicklime (mass ratios of 3, 10, and 20%) to the contaminated soil. The results clearly indicate that quicklime changed the physical properties of the soil, which affected the environmental behaviour of trichloroethylene in the soil. The addition of CaO increased soil temperature and reduced soil moisture to improve the mass transfer of trichloroethylene. In addition, it improved the macroporous cumulative pore volume and average pore size, which increased soil permeability. As soil pH increased, the clay mineral content in the soils decreased, the cation exchange capacity and the redox potential decreased, and the removal of trichloroethylene from the soil was enhanced to a certain extent. After the addition of quicklime, the functional group COO of soil organic matter could interact with calcium ions, which increased soil polarity and promoted the removal of trichloroethylene. Copyright © 2017 Elsevier Ltd. All rights reserved.

  1. Evaluation and performance analysis of hydrocarbon detection methods using hyperspectral data

    OpenAIRE

    Lenz, Andreas; Schilling, Hendrik; Gross, Wolfgang; Middelmann, Wolfgang

    2015-01-01

    Different methods for the detection for hydrocarbons in aerial hyperspectral images are analyzed in this study. The scope is to find a practical method for airborne oil spill mapping on land. Examined are Hydrocarbon index and Hydrocarbon detection index. As well as spectral reidentification algorithms, like Spectral angle mapper, in comparison to the indices. The influence of different ground coverage and different hydrocarbons was tested and evaluated. A ground measurement campaign was cond...

  2. Seismic Evaluation of Hydrocarbon Saturation in Deep-Water Reservoirs

    Energy Technology Data Exchange (ETDEWEB)

    Michael Batzle

    2006-04-30

    During this last period of the ''Seismic Evaluation of Hydrocarbon Saturation in Deep-Water Reservoirs'' project (Grant/Cooperative Agreement DE-FC26-02NT15342), we finalized integration of rock physics, well log analysis, seismic processing, and forward modeling techniques. Most of the last quarter was spent combining the results from the principal investigators and come to some final conclusions about the project. Also much of the effort was directed towards technology transfer through the Direct Hydrocarbon Indicators mini-symposium at UH and through publications. As a result we have: (1) Tested a new method to directly invert reservoir properties, water saturation, Sw, and porosity from seismic AVO attributes; (2) Constrained the seismic response based on fluid and rock property correlations; (3) Reprocessed seismic data from Ursa field; (4) Compared thin layer property distributions and averaging on AVO response; (5) Related pressures and sorting effects on porosity and their influence on DHI's; (6) Examined and compared gas saturation effects for deep and shallow reservoirs; (7) Performed forward modeling using geobodies from deepwater outcrops; (8) Documented velocities for deepwater sediments; (9) Continued incorporating outcrop descriptive models in seismic forward models; (10) Held an open DHI symposium to present the final results of the project; (11) Relations between Sw, porosity, and AVO attributes; (12) Models of Complex, Layered Reservoirs; and (14) Technology transfer Several factors can contribute to limit our ability to extract accurate hydrocarbon saturations in deep water environments. Rock and fluid properties are one factor, since, for example, hydrocarbon properties will be considerably different with great depths (high pressure) when compared to shallow properties. Significant over pressure, on the other hand will make the rocks behave as if they were shallower. In addition to the physical properties, the scale and

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

    Energy Technology Data Exchange (ETDEWEB)

    Hans Peter H. Arp; Gijs D. Breedveld; Gerard Cornelissen [Norwegian Geotechnical Institute (NGI), Oslo (Norway). Department of Environmental Engineering

    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.

  4. Evaluation of environmental samples containing heavy hydrocarbon components in environmental forensic investigations

    Energy Technology Data Exchange (ETDEWEB)

    Raia, J.C.; Blakley, C.R.; Fuex, A.N.; Villalanti, D.C.; Fahrenthold, P.D. [Triton Anal Corp, Houston, TX (United States)

    2004-03-01

    This article presents a procedure to evaluate and characterize environmental samples containing mixtures of hydrocarbons over a wide boiling range of materials that include fuels and other products used in commerce. The range of the method extends to the higher boiling and heavier molecular weight hydrocarbon products in the range of motor oil, bunker fuel, and heavier residue materials. The procedure uses the analytical laboratory technique of high-temperature simulated distillation along with mathematical regression of the analytical data to estimate the relative contribution of individual products in mixtures of hydrocarbons present in environmental samples. An analytical technique to determine hydrocarbon-type distributions by gas chromatography-mass spectrometry with nitric oxide ionization spectrometry evaluation is also presented. This type of analysis allows complex hydrocarbon mixtures to be classified by their chemical composition, or types of hydrocarbons that include paraffins, cycloparaffins, monoaromatics, and polycyclic aromatic hydrocarbons. Characteristic hydrocarbon patterns for example, in the relative distribution of polycyclic aromatic hydrocarbons are valuable for determining the potential origin of materials present in environmental samples. These methods provide quantitative data for hydrocarbon components in mixtures as a function of boiling range and 'hydrocarbon fingerprints' of the types of materials present. This information is valuable in assessing environmental impacts of hydrocarbons at contaminated sites and establishing the liabilities and cost allocations for responsible parties.

  5. Evaluation of Biostimulation (Nutrients) in hydrocarbons contaminated soils by respirometry

    International Nuclear Information System (INIS)

    Garcia, Erika; Roldan, Fabio; Garzon, Laura

    2011-01-01

    The biostimulation process was evaluated in a hydrocarbon contaminated soil by respirometry after amendment with inorganic compound fertilizer (ICF) (N: P: K 28:12:7) and simple inorganic salts (SIS) (NH 4 NO 3 and K 2 HPO 4 ). The soil was contaminated with oily sludge (40.000 MgTPH/Kgdw). The oxygen uptake was measured using two respirometers (HACH 2173b and OXITOP PF 600) during thirteen days (n=3). Two treatments (ICF and SIS) and three controls (abiotic, reference substance and without nutrients) were evaluated during the study. Physicochemical (pH, nutrients, and TPH) and microbiological analysis (heterotrophic and hydrocarbon-utilizing microorganisms) were obtained at the beginning and at the end of each assay. Higher respiration rates were recorded in sis and without nutrient control. Results were 802.28 and 850.72- 1 d-1, MgO 2 kgps - 1d i n HACH, while in OXITOP were 936.65 and 502.05 MgO 2 Kgps respectively. These data indicate that amendment of nutrients stimulated microbial metabolism. ICF had lower respiration rates (188.18 and 139.87 MgO 2 kgps - 1d - 1 i n HACH and OXITOP, respectively) as well as counts; this could be attributed to ammonia toxicity.

  6. Reproductive success and chlorinated hydrocarbon contamination of resident great blue herons (Ardea herodias) from coastal British Columbia, Canada, 1977 to 2000

    International Nuclear Information System (INIS)

    Harris, M.L.; Elliott, J.E.; Butler, R.W.; Wilson, L.K.

    2003-01-01

    Human disturbance and loss of nesting habitat were more important factors than chlorinated hydrocarbons in changing heron reproductive success. - Over the period 1977-2000, eggs of Pacific great blue heron (Ardea herodias fannini) were collected from 23 colonies along the southern coast of British Columbia, Canada, and analyzed for persistent organochlorine (OC) pesticides and polychlorinated biphenyls (PCBs). Concentrations of OC pesticides in eggs declined sharply in the late 1970s, after which there were minimal changes. The sums of PCB congeners were not reduced appreciably during the 1980s and 1990s, but Aroclor 1260 concentrations suggested a sharp decline in PCB contamination of eggs in the late 1970s, similar to that shown for OC pesticides. Eggs collected along or near the Fraser River delta showed higher levels of most pesticides compared to other monitored colonies. Although the delta lands support a long-standing agricultural economy, the primary factors influencing OC levels in the delta colonies were thought to be driven by estuarine processes. We suggest two possible influencing factors were: 1) a greater rate of bioaccumulation in the estuary due to the deposition of particulates collected over a vast area encompassed by the Fraser River watershed; or 2) a higher rate of biomagnification in the estuary due to species differences at lower trophic levels of the heron food chain. Eggs from urban colonies contained higher levels of PCBs. The congener pattern was not clearly different from that observed in less contaminated eggs from rural and pulp mill-influenced colonies, except that colonies in Vancouver had greater proportions of PCB-66, suggesting a local source of Aroclor 1242. Productivity in the coastal heron colonies was highly variable over the period of study, with 71% of recorded colony-wide reproductive failures occurring in colonies near pulp mills. However, the predominant factors influencing reproductive success were probably disturbance

  7. TiO{sub 2} on magnesium silicate monolith: effects of different preparation techniques on the photocatalytic oxidation of chlorinated hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Cardona, Ana I.; Candal, Roberto; Sanchez, Benigno; Avila, Pedro; Rebollar, Moises

    2004-05-01

    In this article, the comparative results of the photocatalytic oxidation of trichloroethylene (TCE) alone and a mixture of chlorinated hydrocarbons (trichloroethylene, perchloroethylene and chloroform) in gas phase, obtained with three different monolithic catalysts in a flat reactor frontally illuminated with a Xenon lamp are presented. The three catalysts incorporate titanium dioxide (TiO{sub 2}) as active phase on a magnesium silicate support, by means of different procedures: (i) incorporation of commercial TiO{sub 2} powder into the silicate matrix ('massic monolith'); (ii) sol-gel coating of the silicate support; (iii) impregnation with a commercial TiO{sub 2} aqueous suspension of the same silicate support. In the first case, the massic monolith was made from a 50:50 w/w mixture of magnesium silicate and 'Titafrance G5' TiO{sub 2} powder. In the second case, a magnesium silicate monolith was coated with several layers of an aqueous TiO{sub 2} sol prepared from hydrolysis and condensation of titanium tetra-isopropoxide (Ti(OC{sub 3}H{sub 7}){sub 4}) in excess of acidified water (acid catalysis). The third catalyst was prepared by impregnating the same silicate support with several layers of 'Titafrance G5' TiO{sub 2} powder water suspension. All the catalysts were thermal treated under comparable conditions in order to fix the TiO{sub 2} active phase to the silicate support. Although the performance of the massic monolith was better than the sol-gel monolith, the latter is of great interest because this technique allows the chemical composition of the active films to be easily modified.

  8. Evaluation of sea water chlorine demand in condenser cooling water at TAPS 1 and 2

    International Nuclear Information System (INIS)

    Papachan, Deepa; Gupta, P.K.; Patil, D.P.; Save, C.B.; Anilkumar, K.R.

    2008-01-01

    To prevent microbiological growth in the condenser tubes, condenser cooling water chlorination is very important. For effective chlorination, chlorine dose rate and frequency of dosing has to be determined on the basis of sea water chlorine demand. TAPS 1 and 2 is located near Arabian sea and draws water from this sea for its condenser cooling. The present practice of chlorine dosing at TAPS 1 and 2, based on the analysis carried out by GE in 1969, is 2500 kg/day/CWpump and 90 kg/day/SSWpump for a contact period of 25 minutes. Normal frequency of dosing is once per 8 hour and booster dose is once in a week at the same rate for 1 hour. The criteria of effective chlorination is to get residual chlorine of 2-3 ppm at the condenser water box outlet during chlorination at water box inlet/CW pump suction header in the recommended dose rate. The other option of chlorination was continuous dosing to get 0.5 ppm residual chlorine. This option has its own limitations as it is more expensive and also that micro organisms get immune to chlorine eventually due to continuous dosing. Nevertheless higher chlorine dosing is detrimental to AI-brass condenser tubes. Therefore the second option was not adopted at TAPS 1 and 2. Tarapur Atomic Power Station-1 is in the process of replacement of condenser tubes due to frequent condenser tube failures in the recent years. It was essential to analyse the present sea water chlorine demand and re-determine the chlorine dose rate because of development of industries under Maharashtra Industrial Development Corporation (MIDC) and simultaneous population growth around this area over a period of three decades. This paper discusses the experimental observations regarding significant change in sea water chlorine demand over this period and the effect of seasonal changes on sea water chlorine demand. (author)

  9. EVALUATION OF THE PROTOCOL FOR THE NATURAL ATTENUATION OF CHLORINATED SOLVENTS: CASE STUDY AT THE TWIN CITIES ARMY AMMUNITION PLANT

    Science.gov (United States)

    At the request of staff in the EPA Regions, EPA?s Office of Research and Development carried out an independent evaluation of the Technical Protocol for Evaluating Natural Attenuation of Chlorinated Solvents in Ground Water (EPA/600/R-98/128). The Protocol was developed around c...

  10. 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.

    Science.gov (United States)

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

    2013-11-08

    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. Copyright © 2013 Elsevier B.V. All rights reserved.

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

    Science.gov (United States)

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

    2014-03-01

    Diclofenac (DCF), a synthetic non-steroidal anti-inflammatory drug, is one of the most frequently detected pharmaceuticals in the aquatic environment. In this work, the mechanism and toxicity of DCF degradation by ClO2 under simulated water disinfection conditions were investigated. Experimental results indicate that rapid and significant oxidation of DCF occurred within the first few minutes; however, its mineralization process was longer than its degradation process. UPLC-MS and (1)H NMR spectroscopy were performed to identify major disinfection byproducts that were generated in three tentative degradation routes. The two main routes were based on initial decarboxylation of DCF on the aliphatic chain and hydroxylation of the phenylacetic acid moiety at the C-4 position. Subsequently, the formed aldehyde intermediates were the starting point for further multistep degradation involving decarboxylation, hydroxylation, and oxidation reactions of CN bond cleavage. The third route was based on transient preservation of chlorinated derivatives resulting from electrophilic attack by chlorine on the aromatic ring, which similarly underwent CN bond cleavage. Microtox bioassay was employed to evaluate the cytotoxicity of solutions treated by ClO2. The formation of more toxic mid-byproducts during the ClO2 disinfection process poses a potential risk to consumers. Copyright © 2013 Elsevier B.V. All rights reserved.

  12. Evaluation of disinfection efficiency in pet's hospital by using chlorine dioxide

    Directory of Open Access Journals (Sweden)

    Ching-Shan Hsu

    2016-07-01

    Full Text Available Microbial aerosols could cause various human and animal health problems and their control is becoming a significant scientific and technological topic for consideration. The main objectives of this study were to monitor bioaerosol levels of the pet's hospital and then to perform disinfection efficiency by applying chlorine dioxide. The air quality within these pet's hospitals should satisfy the guidelines specified by the Taiwan Environmental Protection Administration (TEPA. Accordingly, this study performed an experimental investigation into the efficiency of two different gaseous chlorine dioxide (0.3 mg m−3 treatments in disinfecting a local pet's hospital, namely a single, one-off application and a multiple-daily application. In both cases, the ClO2 was applied using strategically-placed aerosol devices. The air quality before and after disinfection was evaluated by measuring the bioaerosol levels of bacteria and fungi. The experimental results found that the average background levels of bacteria and fungi prior to ClO2 disinfection were found to be 2014 ± 1350 and 1002 ± 669 CFU m−3, respectively. A single ClO2 application was found to total disinfected bacteria and fungi concentration levels by as much as 57.3 and 57.6%. By contrast, a multiple-daily ClO2 application was found to total disinfected bacteria and fungi concentration levels by as much as 65.1 and 57.6%. Among the two disinfection methods, the multiple-daily ClO2 application method was found to yield a higher disinfection efficiency for bacteria, i.e., 16.28 ± 0.92%. Thus, using a ClO2 disinfectant to maintain the air quality is of great importance to reduce infectious diseases in the pet's hospital. Therefore, the results suggest that the air quality guidelines prescribed by the TEPA for pet's hospital and other animal facilities can best be achieved by applying chlorine dioxide at regular intervals. The ClO2 aerosol devices can effectively restrain or

  13. Evaluation of synthetic hydrocarbons for mark-recapture studies on the red milkweed beetle.

    Science.gov (United States)

    Ginzel, Matthew D; Hanks, Lawrence M

    2002-05-01

    This study evaluates the potential for using blends of synthetic hydrocarbons in mark-recapture studies of insects. To test the durability of hydrocarbons, we applied a blend of five straight-chain hydrocarbons (C24, C21, C26. C28, C30) to detached elytra of the red milkweed beetle, Tetraopes tetrophthalmus (Forster) (Coleoptera: Cerambycidae), mounted the elytra on pins, and placed them in an exposed location outdoors. The amount of hydrocarbons on the elytra did not change over time, even after two months of exposure to sun and rain. Synthetic hydrocarbons applied to the elytra of living beetles did not significantly influence their longevity or mating success in a laboratory study. and the amounts of hydrocarbons did not change with age. The invariability of hydrocarbon ratios over time suggests that blends could provide a nearly infinite variety of ratios to mark individual insects uniquely and indelibly with a hydrocarbon "fingerprint." This technique offers a convenient, safe, and durable means of individually marking insects and may find application in field studies of larger bodied insects that are long-lived and sedentary.

  14. Microbial transformation of chlorinated aromatics in sediments

    NARCIS (Netherlands)

    Beurskens, J.E.M.

    1995-01-01

    Numerous contaminants like heavy metals, polycyclic aromatic hydrocarbons (PAHs), chlorinated benzenes (CBs), polychlorinated biphenyls (PCBs), polychlorinated dibenzo- p -dioxins (PCDDs) and polychlorinated furans (PCDFs) are detected in the major rivers in the

  15. Purifying hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Demoulins, H D; Garner, F H

    1923-02-07

    Hydrocarbon distillates, including natural gases and vapors produced by cracking hydrocarbon oils, are desulfurized etc. by treating the vapor with an aqueous alkaline solution of an oxidizing agent. The hydrocarbons may be previously purified by sulfuric acid. In examples aqueous solutions of sodium or calcium hydrochlorite containing 1.5 to 5.0 grams per liter of available chlorine and sufficient alkali to give an excess of 0.1 percent in the spent reagent are preheated to the temperature of the vapor, and either sprayed or atomized into the vapors near the outlet of the dephlegmator or fractionating tower, or passed in countercurrent to the vapors through one or a series of scrubbers.

  16. Demonstration of tools for evaluating the durability of natural attenuation of petroleum hydrocarbons in groundwater

    International Nuclear Information System (INIS)

    Gemoets, J.; Ceuster, T. de; Vandervelpen, B.; Gutschoven, K.

    2005-01-01

    The dominant process for natural attenuation of petroleum hydrocarbons such as BTEX or alkanes in groundwater is microbial oxidation. In many instances demonstration of natural attenuation is limited to historic trend analysis of pollutant concentrations and analyses of electron acceptors and their reduced forms as secondary evidence for NA. By doing so one can demonstrate that biodegradation processes are occurring naturally. However, this approach does not ensure that natural attenuation processes will continue to occur to the extent that is required to sustain control of the complete pollutant mass over a long time. A sufficient supply of naturally occurring oxidants (electron acceptors) is required to enable adequate microbial oxidation of hydrocarbons. Naturally occurring oxidants for microbial oxidation are oxygen, nitrate, ferric iron, manganese(IV), sulfate and carbon dioxide. At many sites iron(III) may be the most abundant electron acceptor, as it may be present in large quantities in the solid aquifer materials. However, only a fraction of it may be available for micro-organisms. Thus far this parameter is rarely analyzed during site investigation programs for MNA. Bio-available iron may also play an important role in the feasibility of complete microbial dehalogenation of chlorinated solvents. We will present results of a research project in which we have evaluated three methods for determining the quantity of bio-available ferric iron in solid aquifer material samples. These were mild acid extraction followed by spectrophotometry, redox titration with titanium(III)-EDTA and a commercially available enzymatic test kit (BAFeIII assay). The results will be compared, considering implications for practical implementation. The program is being carried out for two petrol station sites for which MNA has been applied as the groundwater remediation method. At each site three soil boring are performed across a depth trajectory below the groundwater table

  17. Demonstration of tools for evaluating the durability of natural attenuation of petroleum hydrocarbons in groundwater

    Energy Technology Data Exchange (ETDEWEB)

    Gemoets, J.; Ceuster, T. de; Vandervelpen, B.; Gutschoven, K. [Haskoning Belgium (Belgium)

    2005-07-01

    The dominant process for natural attenuation of petroleum hydrocarbons such as BTEX or alkanes in groundwater is microbial oxidation. In many instances demonstration of natural attenuation is limited to historic trend analysis of pollutant concentrations and analyses of electron acceptors and their reduced forms as secondary evidence for NA. By doing so one can demonstrate that biodegradation processes are occurring naturally. However, this approach does not ensure that natural attenuation processes will continue to occur to the extent that is required to sustain control of the complete pollutant mass over a long time. A sufficient supply of naturally occurring oxidants (electron acceptors) is required to enable adequate microbial oxidation of hydrocarbons. Naturally occurring oxidants for microbial oxidation are oxygen, nitrate, ferric iron, manganese(IV), sulfate and carbon dioxide. At many sites iron(III) may be the most abundant electron acceptor, as it may be present in large quantities in the solid aquifer materials. However, only a fraction of it may be available for micro-organisms. Thus far this parameter is rarely analyzed during site investigation programs for MNA. Bio-available iron may also play an important role in the feasibility of complete microbial dehalogenation of chlorinated solvents. We will present results of a research project in which we have evaluated three methods for determining the quantity of bio-available ferric iron in solid aquifer material samples. These were mild acid extraction followed by spectrophotometry, redox titration with titanium(III)-EDTA and a commercially available enzymatic test kit (BAFeIII assay). The results will be compared, considering implications for practical implementation. The program is being carried out for two petrol station sites for which MNA has been applied as the groundwater remediation method. At each site three soil boring are performed across a depth trajectory below the groundwater table

  18. Evaluating the Environmental Fate of Short-Chain Chlorinated Paraffins (SCCPs) in the Nordic Environment Using a Dynamic Multimedia Model

    OpenAIRE

    Krogseth, Ingjerd Sunde; Breivik, Knut; Arnot, Jon A; Wania, Frank; Borgen, Anders; Schlabach, Martin

    2013-01-01

    Short chain chlorinated paraffins (SCCPs) raise concerns due to their potential for persistence, bioaccumulation, long-range transport and adverse effects. An understanding of their environmental fate remains limited, partly due to the complexity of the mixture. The purpose of this study was to evaluate whether a mechanistic, integrated, dynamic environmental fate and bioaccumulation multimedia model (CoZMoMAN) can reconcile what is known about environmental emissions and human exposure of SC...

  19. Evaluating the effects of granular and membrane filtrations on chlorine demand in drinking water.

    Science.gov (United States)

    Jegatheesan, Veeriah; Kim, Seung Hyun; Joo, C K; Gao, Baoyu

    2009-01-01

    In this study, chlorine decay experiments were conducted for the raw water from Nakdong River that is treated by Chilseo Water Treatment Plant (CWTP) situated in Haman, Korea as well as the effluents from sand and granular activated carbon (GAC) filters of CWTP and fitted using a chlorine decay model. The model estimated the fast and slow reacting nitrogenous as well as organic/inorganic compounds that were present in the water. It was found that the chlorine demand due to fast and slow reacting (FRA and SRA) organic/inorganic substances was not reduced significantly by sand as well as GAC filters. However, the treated effluents from those filters contained FRA and SRA that are less reactive and had small reaction rate constants. For the effluents from microfiltration, ultrafiltration, and nanofiltration the chlorine demand because FRA and SRA were further reduced but the reaction rate constants were larger compared to those of sand and GAC filter effluents. This has implications in the formation of disinfection by products (DBPs). If DBPs are assumed to form due to the interactions between chlorine and SRA, then it is possible that the DBP formation potential in the effluents from membrane filtrations could be higher than that in the effluents from granular media filters.

  20. Statistical evaluation of variables affecting occurrence of hydrocarbons in aquifers used for public supply, California

    Science.gov (United States)

    Landon, Matthew K.; Burton, Carmen A.; Davis, Tracy A.; Belitz, Kenneth; Johnson, Tyler D.

    2014-01-01

    The variables affecting the occurrence of hydrocarbons in aquifers used for public supply in California were assessed based on statistical evaluation of three large statewide datasets; gasoline oxygenates also were analyzed for comparison with hydrocarbons. Benzene is the most frequently detected (1.7%) compound among 17 hydrocarbons analyzed at generally low concentrations (median detected concentration 0.024 μg/l) in groundwater used for public supply in California; methyl tert-butyl ether (MTBE) is the most frequently detected (5.8%) compound among seven oxygenates analyzed (median detected concentration 0.1 μg/l). At aquifer depths used for public supply, hydrocarbons and MTBE rarely co-occur and are generally related to different variables; in shallower groundwater, co-occurrence is more frequent and there are similar relations to the density or proximity of potential sources. Benzene concentrations are most strongly correlated with reducing conditions, regardless of groundwater age and depth. Multiple lines of evidence indicate that benzene and other hydrocarbons detected in old, deep, and/or brackish groundwater result from geogenic sources of oil and gas. However, in recently recharged (since ~1950), generally shallower groundwater, higher concentrations and detection frequencies of benzene and hydrocarbons were associated with a greater proportion of commercial land use surrounding the well, likely reflecting effects of anthropogenic sources, particularly in combination with reducing conditions.

  1. Analyzing Environmental Policies for Chlorinated Solvents with a Model of Markets and Regulations

    Science.gov (United States)

    1991-01-01

    chlorine, fluorine , bromine, and iodine. Another broad term is chlorocarbons (fluorocarbons), which indicates the chlorinated ( fluorinated ) hydrocarbons... varnishes , and lacquers (Wolf, Yazdani, and Yates, 1990b). Process Substitutes. The only process modifications that are available for consumer paint

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

    Science.gov (United States)

    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

  3. Evaluation of cooling water treatment programme at RAPS-3 and 4 with reference to chlorination and microbial control

    International Nuclear Information System (INIS)

    Kora, Aruna Jyothi; Rao, T.S.; Narasimhan, S.V.

    2008-01-01

    Water from Rana Pratap Sagar Lake is used in Rajasthan Atomic Power Station (RAPS) units 3 and 4 for cooling the condenser system. As the lake water is rich in nutrients and microflora, investigations were carried out on the nutrient quality, microflora distribution and chlorine decay to evaluate the cooling water treatment programme. Algal growth in emergency storage makeup water pools, weed growth on the cooling tower decks and biofilm growth on various materials (carbon steel, stainless steel, admiralty brass and cupronickel) were studied with an objective to understand the reasons for corrosion and failure of fire water pipeline. Visual examination showed that the emergency makeup water pools were infested with green algae and cyano-bacterial mats. Some algal growth was observed on induced draft cooling tower-3 structures. The bacterial counts in various water samples were low, except in emergency makeup water pool. Sulphate reducing bacteria (SRB) were present in makeup and demineralised waters. Chlorophyll pigment analysis showed that the makeup and emergency storage water pool had abundant algal growth. To prevent biofouling, chlorine is dosed at the rate of 7 kg/hr for 10 minutes; free residual oxidant (FRO) and chlorine decay were monitored at regular intervals. After 24 hrs, biofilm thickness on different materials ranged from 27-45 μm. However, the thickness was reduced by 50 % after exposure to 2 ppm of chlorine for 15 minutes. In further investigations, it was found that the anion resin beads of demineraliser plant were infested with filamentous microbes. Hence, It is recommended to treat the feed water of DM plant. Tubercles were observed inside the failed fire water carbon steel pipeline and on removing the tubercles concentric ring patterns, typical signatures of SRB corrosion were observed. For controlling the biofouling problem in the cooling water system, it is recommended to maintain a chlorine dose of 2.3 ppm (which gives 0.8 ppm FRO) for two

  4. On the efficiency of the hybrid and the exact second-order sampling formulations of the EnKF: a reality-inspired 3-D test case for estimating biodegradation rates of chlorinated hydrocarbons at the port of Rotterdam

    KAUST Repository

    El Gharamti, Mohamad

    2016-11-15

    This study considers the assimilation problem of subsurface contaminants at the port of Rotterdam in the Netherlands. It involves the estimation of solute concentrations and biodegradation rates of four different chlorinated solvents. We focus on assessing the efficiency of an adaptive hybrid ensemble Kalman filter and optimal interpolation (EnKF-OI) and the exact second-order sampling formulation (EnKFESOS) for mitigating the undersampling of the estimation and observation errors covariances, respectively. A multi-dimensional and multi-species reactive transport model is coupled to simulate the migration of contaminants within a Pleistocene aquifer layer located around 25 m below mean sea level. The biodegradation chain of chlorinated hydrocarbons starting from tetrachloroethene and ending with vinyl chloride is modeled under anaerobic environmental conditions for 5 decades. Yearly pseudo-concentration data are used to condition the forecast concentration and degradation rates in the presence of model and observational errors. Assimilation results demonstrate the robustness of the hybrid EnKF-OI, for accurately calibrating the uncertain biodegradation rates. When implemented serially, the adaptive hybrid EnKF-OI scheme efficiently adjusts the weights of the involved covariances for each individual measurement. The EnKFESOS is shown to maintain the parameter ensemble spread much better leading to more robust estimates of the states and parameters. On average, a well tuned hybrid EnKF-OI and the EnKFESOS respectively suggest around 48 and 21 % improved concentration estimates, as well as around 70 and 23 % improved anaerobic degradation rates, over the standard EnKF. Incorporating large uncertainties in the flow model degrades the accuracy of the estimates of all schemes. Given that the performance of the hybrid EnKF-OI depends on the quality of the background statistics, satisfactory results were obtained only when the uncertainty imposed on the background

  5. Chlorine poisoning

    Science.gov (United States)

    ... gas) Gas released when opening a partially filled industrial container of chlorine tablets that have been sitting ... change in acid level of the blood (pH balance), which leads to damage in all of the ...

  6. Evaluating potential chlorinated methanes degradation mechanisms and treatments in interception trenches filled with concrete-based construction wastes

    Science.gov (United States)

    Rodríguez-Fernandez, Diana; Torrentó, Clara; Rosell, Mònica; Audí-Miró, Carme; Soler, Albert

    2014-05-01

    conditions in the trenches with in situ chemical oxidation (ISCO), which would be able to remove the rest of the accompanying pollutants, is proposed and merits evaluation. Preliminary batch experiments were performed to evaluate the feasibility of different chemical oxidation reactions (permanganate, persulphate, hydrogen peroxide and Fenton) on the complex contaminated recharge water which were, in general, more effective for degrading the chlorinated ethenes than for the chlorinated methanes (Torrentó et al. EGU 2012). Therefore, this study seeks to improve the understanding of CF and CT degradation mechanisms/processes that are going on in the interception trenches as well as to select between the two most effective chemical oxidation remediation treatments (persulphate and permanganate) taking into account their efficiency respect the chlorinated methanes removal, the generated acute toxicity and the applicability of the carbon isotopic fractionation as an indicator of the effectiveness of the future in situ remediation. Additionally, ongoing batch experiments are expected to elucidate if CT is undergoing abiotic reductive dechlorination by Fe-bearing minerals such as hydrophobic green rust (Ayala-Luis et al., 2012) which transform CT into non-chlorinated substances such as formic acid and carbon monoxide. This unstable iron compound might be formed in the interception trenches during chloride induced corrosion of iron mineral phases present in the concrete-based construction wastes (Sagoe-Crentsil and Glasser, 1993). The role of other minerals like iron oxy-hydroxides, carbonates or sulphides cannot be discarded at all. The potential of δ13C values to assess the efficiency of this abiotic CT degradation reaction will be also evaluated. References Ayala-Luis, K.; Cooper, N.; Bender C. and Hansen. H. (2012) Efficient dechlorination of carbon tetrachloride by hydrophobic green rust intercaled with dodecanoate anions. Environmental Science & Technology 46, 3390

  7. Evaluation of genotoxic effects caused by extracts of chlorinated drinking water using a combination of three different bioassays.

    Science.gov (United States)

    Zeng, Qiang; Zhang, Shao-Hui; Liao, Jing; Miao, Dong-Yue; Wang, Xin-Yi; Yang, Pan; Yun, Luo-Jia; Liu, Ai-Lin; Lu, Wen-Qing

    2015-10-15

    Potential genotoxic effects of chlorinated drinking water now are of a great concern. In this study, raw water, finished water, and tap water from a water plant in Wuhan, China were collected in two different sampling times of the year (January and July). Genotoxic effects of water extracts were evaluated using a combination of three different bioassays: SOS/umu test, HGPRT gene mutation assay, and micronucleus assay, which were separately used to detect DNA damage, gene mutation, and chromosome aberration. The results of three different bioassays showed that all water samples in January and July induced at least one types of genotoxic effects, of which the DNA-damage effects were all detectable. The levels of DNA-damage effects and gene-mutation effects of finished water and tap water in January were higher than those in July. Chlorination could increase the DNA-damage effects of drinking water in January and the gene-mutation effects of drinking water in both January and July, but did not increase the chromosome-aberration effects of drinking water in both January and July. Our results highlighted the importance of using a combination of different bioassays to evaluate the genotoxicity of water samples in different seasons. Copyright © 2015 Elsevier B.V. All rights reserved.

  8. Hydrocarbon source rock potential evaluation of the Late Paleocene ...

    Indian Academy of Sciences (India)

    63

    research is available on its source rock potential evaluation at Nammal Gorge Section in the Salt. Range, Potwar Basin .... methods of Tucker (2003) and Assaad (2008) have been followed. A total of fifteen ..... Business Media. Baker D M, Lillie ...

  9. Evaluation of 10 aliphatic halogenated hydrocarbons in the mouse bone marrow micronucleus test.

    Science.gov (United States)

    Crebelli, R; Carere, A; Leopardi, P; Conti, L; Fassio, F; Raiteri, F; Barone, D; Ciliutti, P; Cinelli, S; Vericat, J A

    1999-03-01

    Ten halogenated aliphatic hydrocarbons (carbon tetrachloride, 1-chlorohexane, 2,3-dichlorobutane, 1,2-dichloroethane, 1,2-dichloroethylene, 1,3-dichloropropane, hexachloroethane, 1,1,2-trichloroethane, 1,2,3-trichloropropane and 1,1,3-trichloropropene), previously assayed in genetic assays in fungi, were evaluated in the mouse bone marrow micronucleus test in order to assess their genotoxicity in vivo. All chemicals were administered once i.p. at 40 and 70-80% of their respective LD50 to male and female CD-1 mice, 24 and 48 h before killing. All treatments produced evident clinical symptoms, but no marked depression of bone marrow proliferation. No statistically significant increases in the incidence of micronucleated polychromatic erythrocytes over the control values were observed at any sampling time with any of the 10 halogenated hydrocarbons assayed. The comparison of the results obtained in this study with the findings provided by in vitro micronucleus assays on the same chemicals, reported by other authors, indicate that mouse bone marrow is weakly sensitive to the genotoxic effects induced by halogenated hydrocarbons in other test systems. This suggests that the role of such an assay in carcinogen screening may be questionable for this chemical class. An examination of mouse bone marrow micronucleus test results with the halogenated aliphatic hydrocarbons classified as carcinogens by IARC supports this conclusion.

  10. Development of a solid-phase microextraction-based method for sampling of persistent chlorinated hydrocarbons in an urbanized coastal environment.

    Science.gov (United States)

    Zeng, Eddy Y; Tsukada, David; Diehl, Dario W

    2004-11-01

    Solid-phase microextraction (SPME) has been used as an in situ sampling technique for a wide range of volatile organic chemicals, but SPME field sampling of nonvolatile organic pollutants has not been reported. This paper describes the development of an SPME-based sampling method employing a poly(dimethylsiloxane) (PDMS)-coated (100-microm thickness) fiber as the sorbent phase. The laboratory-calibrated PDMS-coated fibers were used to construct SPME samplers, and field tests were conducted at three coastal locations off southern California to determine the equilibrium sampling time and compare the efficacy of the SPME samplers with that of an Infiltrex 100 water pumping system (Axys Environmental Systems Ltd., Sidney, British Columbia, Canada). p,p'-DDE and o,p'-DDE were the components consistently detected in the SPME samples among 42 polychlorinated biphenyl congeners and 17 chlorinated pesticidestargeted. SPME samplers deployed attwo locations with moderate and high levels of contamination for 18 and 30 d, respectively, attained statistically identical concentrations of p,p'-DDE and o,p'-DDE. In addition, SPME samplers deployed for 23 and 43 d, respectively, at a location of low contamination also contained statistically identical concentrations of p,p'-DDE. These results indicate that equilibrium could be reached within 18 to 23 d. The concentrations of p,p'-DDE, o,p'-DDE, or p,p'-DDD obtained with the SPME samplers and the Infiltrex 100 system were virtually identical. In particular, two water column concentration profiles of p,p'-DDE and o,p'-DDE acquired by the SPME samplers at a highly contaminated site on the Palos Verdes Shelf overlapped with the profiles obtained by the Infiltrex 100 system in 1997. The field tests not only reveal the advantages of the SPME samplers compared to the Infiltrex 100 system and other integrative passive devices but also indicate the need to improve the sensitivity of the SPME-based sampling technique.

  11. Coupling spectroscopic and chromatographic techniques for evaluation of the depositional history of hydrocarbons in a subtropical estuary

    International Nuclear Information System (INIS)

    Martins, César C.; Doumer, Marta E.; Gallice, Wellington C.; Dauner, Ana Lúcia L.; Cabral, Ana Caroline; Cardoso, Fernanda D.

    2015-01-01

    Spectroscopic and chromatographic techniques can be used together to evaluate hydrocarbon inputs to coastal environments such as the Paranaguá estuarine system (PES), located in the SW Atlantic, Brazil. Historical inputs of aliphatic hydrocarbons (AHs) and polycyclic aromatic hydrocarbons (PAHs) were analyzed using two sediment cores from the PES. The AHs were related to the presence of biogenic organic matter and degraded oil residues. The PAHs were associated with mixed sources. The highest hydrocarbon concentrations were related to oil spills, while relatively low levels could be attributed to the decrease in oil usage during the global oil crisis. The results of electron paramagnetic resonance were in agreement with the absolute AHs and PAHs concentrations measured by chromatographic techniques, while near-infrared spectroscopy results were consistent with unresolved complex mixture (UCM)/total n-alkanes ratios. These findings suggest that the use of a combination of techniques can increase the accuracy of assessment of contamination in sediments. - Highlights: • Historical inputs of hydrocarbons in a subtropical estuary were evaluated. • Spectroscopic and chromatographic methods were used in combination. • High hydrocarbon concentrations were related to anthropogenic activities. • Low hydrocarbon levels could be explained by the 1970s global oil crisis. - Spectroscopic and chromatographic techniques could be used together to evaluate hydrocarbon inputs to coastal environments

  12. Ready-to-eat vegetables production with low-level water chlorination. An evaluation of water quality, and of its impact on end products.

    Science.gov (United States)

    D'Acunzo, Francesca; Del Cimmuto, Angela; Marinelli, Lucia; Aurigemma, Caterina; De Giusti, Maria

    2012-01-01

    We evaluated the microbiological impact of low-level chlorination (1 ppm free chlorine) on the production of ready-to-eat (RTE) vegetables by monitoring the microbiological quality of irrigation and processing water in two production plants over a 4-season period, as well as the microbiological quality of unprocessed vegetables and RTE product. Water samples were also characterized in terms of some chemical and physico-chemical parameters of relevance in chlorination management. Both producers use water with maximum 1 ppm free chlorine for vegetables rinsing, while the two processes differ by the number of washing cycles. Salmonella spp and Campylobacter spp were detected once in two different irrigation water samples out of nine from one producer. No pathogens were found in the vegetable samples. As expected, the procedure encompassing more washing cycles performed slightly better in terms of total mesophilic count (TMC) when comparing unprocessed and RTE vegetables of the same batch. However, data suggest that low-level chlorination may be insufficient in preventing microbial build-up in the washing equipment and/or batch-to batch cross-contamination.

  13. IMPLICATIONS OF MICROBIAL ADHESION TO HYDROCARBONS FOR EVALUATING CELL-SURFACE HYDROPHOBICITY .1. ZETA-POTENTIALS OF HYDROCARBON DROPLETS

    NARCIS (Netherlands)

    BUSSCHER, HJ; VANDEBELTGRITTER, B; VANDERMEI, HC

    1995-01-01

    Microbial adhesion to hydrocarbons (MATH) is generally considered to be a measure of the organisms cell surface hydrophobicity. As microbial adhesion is a complicated interplay of long-range van der Waals and electrostatic forces and various short-range interactions, the above statement only holds

  14. River sediment (S-37)--a new analytical quality control material ensuring comparability of chlorinated hydrocarbon analysis during an international environmental study in China.

    Science.gov (United States)

    Gawlik, B M; Martens, D; Henkelmann, B; Schramm, K W; Kettrup, A; Muntau, H

    2000-06-01

    A sediment reference material (S-37) was prepared as analytical quality control material to be used within an international project on polychlorinated hydrocarbon analysis in two Chinese rivers. The raw material was sampled during a cruise on Yangtse River and transported afterwards to the JRC Ispra for further processing. The material was treated according to the general principles applicable for candidate reference material production. After a thorough homogeneity study of the bulk the material was bottled. A total of 1,080 bottles each containing 50 g of dry sediment powder was obtained. Final homogeneity and stability testing proved the material to be fit for the purpose. Isotope dilution GC/MS was used to establish target values for pentachlorobenzene (1.17 +/- 0.08 ng/g), hexachlorobenzene (3.60 +/- 0.17 ng/g), octachlorostyrene (0.19 +/- 0.01 ng/g), pentachloroanisole (0.52 +/- 0.02 ng/g), alpha-HCH (0.70 +/- 0.05 ng/g), beta-HCH (1.38 +/- 0.18 ng/g), gamma-HCH (0.83 +/- 038 ng/g), 2,4'-DDT (0.36 +/- 0.04 ng/g), 2,4'-DDE (0.29 +/- 0.02 ng/g), 2,4'-DDD (0.49 +/- 0.02), 4,4'-DDT (3.42 +/- 0.47 ng/g), 4,4'-DDD (1.29 +/- 0.17 ng/g), PCB 28 (0.11 +/- 0.01 ng/g), PCB 52 (0.09 +/- 0.003 ng/g), PCB 101 (0.07 +/- 0.003 ng/g), PCB 138 (0.06 +/- 0.003 ng/g) and PCB 153 (0.06 +/- 0.003 ng/g). Furthermore, indicative values for major and minor constituents as well as for polychlorinated dibenzodioxines and -furanes were measured.

  15. Bacterial oxidation of low-chlorinated compounds under anoxic conditions

    NARCIS (Netherlands)

    Dijk, J.A.

    2005-01-01

    Chlorinated hydrocarbons belong to the most frequently encountered contaminants in soil and groundwater. Many of them were found to be toxic and recalcitrant, which causes a potential threat to the environment. Therefore, it is of great importance that sites contaminated with chlorinated

  16. Removal of Chlorinated Chemicals in H2 Feedstock Using Modified Activated Carbon

    Directory of Open Access Journals (Sweden)

    Prapaporn Luekittisup

    2015-01-01

    Full Text Available Activated carbon (GAC was impregnated by sodium and used as adsorbent to remove chlorinated hydrocarbon (CHC gases contaminated in H2 feedstock. The adsorption was carried out in a continuous packed-bed column under the weight hourly space velocity range of 0.8–1.0 hr−1. The adsorption capacity was evaluated via the breakthrough curves. This modified GAC potentially adsorbed HCl and VCM of 0.0681 gHCl/gadsorbent and 0.0026 gVCM/gadsorbent, respectively. It showed higher adsorption capacity than SiO2 and Al2O3 balls for both organic and inorganic CHCs removal. In addition, the kinetic adsorption of chlorinated hydrocarbons on modified GAC fit well with Yoon-Nelson model.

  17. Evaluation of benzodiazepines and zolpidem in nails and their stability after prolonged exposure to chlorinated water.

    Science.gov (United States)

    Moretti, Matteo; Andrello, Luisa; Visonà, Silvia; Vignali, Claudia; Groppi, Angelo; Freni, Francesca; Osculati, Antonio; Tajana, Luca; Morini, Luca

    2018-04-15

    The study aims the development and validation of a LC-MS/MS method for the identification and quantification of benzodiazepines and zolpidem in nails as alternative keratinized matrix to hair in long-term monitoring of anxiolytic and hypnotic drugs. Both fingernail and toenail samples (1-2 mm) were collected by clipping the excess overhang of the nail from volunteers and from postmortem cases. They were washed twice with organic solvents, dried under nitrogen stream, pulverized, immersed in a methanol solution (internal standard: diazepam-D5) and sonicated up to two hours. The solution was then direct injected in the LC-MS/MS system. Mass spectrometry was set in MRM mode, selecting two transitions for each substance. 32 analytes among benzodiazepines, metabolites and hypnotics were included in the list. The method fulfilled the internationally required criteria for validation. Limits of detection ranged from 0.03 pg/mg (zolpidem) to 13.1 pg/mg (bromazepam). 9 subjects under therapy were positive at 7 different benzodiazepines and/or metabolites (lorazepam, desalkylflurazepam, bromazepam, diazepam, alprazolam, lormetazepam and prazepam), while 5 molecules were measured in 4 postmortem cases (diazepam, desmethyldiazepam, delorazepam, 7-aminoclonazepam and zolpidem). In vitro experiments on eight authentic samples suggested that benzodiazepines in nails are influenced by the prolonged exposure to chlorinated water. Copyright © 2018 Elsevier B.V. All rights reserved.

  18. Evaluation of polyethersulfone performance for the microextraction of polar chlorinated herbicides from environmental water samples.

    Science.gov (United States)

    Prieto, Ailette; Rodil, Rosario; Quintana, José Benito; Cela, Rafael; Möder, Monika; Rodríguez, Isaac

    2014-05-01

    In this work, the suitability of bulk polyethersulfone (PES) for sorptive microextraction of eight polar, chlorinated phenoxy acids and dicamba from environmental water samples is assessed and the analytical features of the optimized method are compared to those reported for other microextraction techniques. Under optimized conditions, extractions were performed with samples (18 mL) adjusted at pH 2 and containing a 30% (w/v) of sodium chloride, using a tubular PES sorbent (1 cm length × 0.7 mm o.d., sorbent volume 8 µL). Equilibrium conditions were achieved after 3h of direct sampling, with absolute extraction efficiencies ranging from 39 to 66%, depending on the compound. Analytes were recovered soaking the polymer with 0.1 mL of ethyl acetate, derivatized and determined by gas chromatography-mass spectrometry (GC-MS). Achieved quantification limits (LOQs) varied between 0.005 and 0.073 ng mL(-1). After normalization with the internal surrogate (IS), the efficiency of the extraction was only moderately affected by the particular characteristics of different water samples (surface and sewage water); thus, pseudo-external calibration, using spiked ultrapure water solutions, can be used as quantification technique. The reduced cost of the PES polymer allowed considering it as a disposable sorbent, avoiding variations in the performance of the extraction due to cross-contamination problems and/or surface modification with usage. Copyright © 2014 Elsevier B.V. All rights reserved.

  19. Evaluating the environmental fate of short-chain chlorinated paraffins (SCCPs) in the Nordic environment using a dynamic multimedia model.

    Science.gov (United States)

    Krogseth, Ingjerd S; Breivik, Knut; Arnot, Jon A; Wania, Frank; Borgen, Anders R; Schlabach, Martin

    2013-12-01

    Short chain chlorinated paraffins (SCCPs) raise concerns due to their potential for persistence, bioaccumulation, long-range transport and adverse effects. An understanding of their environmental fate remains limited, partly due to the complexity of the mixture. The purpose of this study was to evaluate whether a mechanistic, integrated, dynamic environmental fate and bioaccumulation multimedia model (CoZMoMAN) can reconcile what is known about environmental emissions and human exposure of SCCPs in the Nordic environment. Realistic SCCP emission scenarios, resolved by formula group, were estimated and used to predict the composition and concentrations of SCCPs in the environment and the human food chain. Emissions at the upper end of the estimated range resulted in predicted total concentrations that were often within a factor of 6 of observations. Similar model performance for a complex group of organic contaminants as for the well-known polychlorinated biphenyls strengthens the confidence in the CoZMoMAN model and implies a relatively good mechanistic understanding of the environmental fate of SCCPs. However, the degree of chlorination predicted for SCCPs in sediments, fish, and humans was higher than observed and poorly established environmental half-lives and biotransformation rate constants contributed to the uncertainties in the predicted composition and ∑SCCP concentrations. Improving prediction of the SCCP composition will also require better constrained estimates of the composition of SCCP emissions. There is, however, also large uncertainty and lack of coherence in the existing observations, and better model-measurement agreement will require improved analytical methods and more strategic sampling. More measurements of SCCP levels and compositions in samples from background regions are particularly important.

  20. Evaluation of gaseous chlorine dioxide for the inactivation of Tulane virus on blueberries.

    Science.gov (United States)

    Kingsley, David H; Pérez-Pérez, Rafael E; Niemira, Brendan A; Fan, Xuetong

    2018-05-20

    To determine the effectiveness of gaseous chlorine dioxide (gClO 2 ) against a human norovirus surrogate on produce, gClO 2 was generated and applied to Tulane virus-coated blueberries in a 240 ml-treatment chamber. gClO 2 was produced by an acidifying sodium chlorite solution. Initial assessments indicated that blueberries treated with gClO 2 generated from ≤1 mg acidified sodium chlorite in the small chamber appeared unaffected while gClO 2 generated from ≥10 mg of acidified sodium chlorite solution altered the appearance and quality of the blueberries. Treatments of inoculated blueberries with gClO 2 generated from 0.1 mg sodium chlorite reduced the virus populations by >1 log after exposure for 30 to 330 min. For the 1 mg sodium chlorite treatments, the virus populations were reduced by >2.2 log after 15 min exposure and to non-detectable levels (>3.3 logs reductions) after 180 min exposure. Measured concentrations of gClO 2 peaked in the treatment chamber at 0.9 μg/l after 10 min for 0.1 mg treatments and 600 μg/l after around 20 min for 1 mg treatment. Overall results indicate that gClO 2 could be a feasible waterless intervention for blueberries and other produce. Published by Elsevier B.V.

  1. Process engineering and economic evaluations of diaphragm and membrane chlorine cell technologies. Final report

    Energy Technology Data Exchange (ETDEWEB)

    1980-12-01

    The chlor-alkali manufacturing technologies of (1), diaphragm cells (2), current technology membrane cells (3), catalytic cathode membrane cells (4), oxygen-cathode membrane cells and to a lesser extent several other related emerging processes are studied. Comparisons have been made on the two bases of (1) conventional industrial economics, and (2) energy consumption. The current diaphragm cell may have a small economic advantage over the other technologies at the plant size of 544 metric T/D (600 T/D). The three membrane cells all consume less energy, with the oxygen-cathode cell being the lowest. The oxygen-cathode cell appears promising as a low energy chlor-alkali cell where there is no chemical market for hydrogen. Federal funding of the oxygen-cathode cell has been beneficial to the development of the technology, to electrochemical cell research, and may help maintain the US's position in the international chlor-alkali technology marketplace. Tax law changes inducing the installation of additional cells in existing plants would produce the quickest reduction in power consumption by the chlor-alkali industry. Alternative technologies such as the solid polymer electrolyte cell, the coupling of diaphragm cells with fuel cells and the dynamic gel diaphragm have a strong potential for reducing chloralkali industry power consumption. Adding up all the recent and expected improvements that have become cost-effective, the electrical energy required to produce a unit of chlorine by 1990 should be only 50% to 60% of that used in 1970. In the United States the majority of the market does not demand salt-free caustic. About 75% of the electrolytic caustic is produced in diaphragm cells and only a small part of that is purified. This study indicates that unless membrane cell costs are greatly reduced or a stronger demand develops for salt-free caustic, the diaphragm cells will remain competitive. (WHK)

  2. Three versus five micrometer chlorinated polysaccharide-based packings in chiral capillary electrochromatography: performance evaluation.

    Science.gov (United States)

    Hendrickx, Ans; De Klerck, Katrijn; Mangelings, Debby; Clincke, Lies; Heyden, Yvan Vander

    2014-01-01

    In this study, a test set of 44 nonacidic compounds was analyzed on four 3 µm chlorinated polysaccharide-based chiral stationary phases with cellulose tris (3-chloro-4-methylphenylcarbamate) (Lux Cellulose-2®; LC2), amylose tris (5-chloro-2-methylphenylcarbamate) (Lux Amylose-2®, LA2), cellulose tris (4-chloro-3-methylphenylcarbamate) (Lux Cellulose-4®; LC4) and cellulose tris (3,5-dichlorophenylcarbamate) (Sepapak-5®, Sp5) as selectors. The analysis times, retention factors, efficiencies and enantioselectivities were compared with the results obtained on their 5 µm analogs. All 3 µm packings, except for LA2, individually separated more compounds than their 5 µm analogs. When the cumulative success rates on the 3 and 5 µm packings were considered, it was observed that they were similar for both particle sizes; the combination of three or four 5 µm columns separated one compound more from the considered test set than that of the same number of 3 µm columns. Furthermore, it was observed that the 3 and 5 µm packings showed some complementarity. Only four compounds were not separated on any of the columns, while the use of only either the 3 or 5 µm columns resulted in 10 and nine not-separated compounds, respectively. The analyses on 5 µm LC2 and Sp5 were faster than on their 3 µm analogs. For LC4 the 3 µm packing showed the shortest analysis times and diverse analysis times for both particle sizes were obtained on LA2. Furthermore, three out of four 3 µm packings, that is, LC2, LC4, and Sp5, were found to be more efficient than their 5 µm analogs. Copyright © 2013 John Wiley & Sons, Ltd.

  3. Studies on chlorinated bromide salt for microfouling control

    International Nuclear Information System (INIS)

    Satpathy, K.K.; Rajmohan, R.; Rao, T.S.; Nair, K.V.K.; Mathur, P.K.

    1995-01-01

    The Fast Breeder Test reactor (FBTR) at Kalpakkam has been facing various problems in cooling water systems in spite of intermittent chlorination.Effects of chlorinated-bromide mixture was evaluated against heterotrophic bacteria (TVC) and iron oxidising bacteria (IOB) vis-a-vis chlorine. Results indicated that chlorinated-bromide mixture was far superior (2 orders of magnitude for TVC and 2 times for IOB) to chlorine in microfouling control. Results also showed that at bromide to chlorine ratio of one effectiveness of chlorinated-bromide was at its maximum. (author). 9 refs., 1 tab

  4. Polycyclic aromatic hydrocarbons levels evaluation in urban area after October 23rd 1998 promulgation

    International Nuclear Information System (INIS)

    Galimberti, E.; Baroni, R.; Villa, V.; Sesana, G.

    1999-01-01

    This paper reports the result concerning the air quality evaluation in an urban centre in the hinterland of Milan., with an high population density and an intense road traffic, relatively to polycyclic aromatic hydrocarbons (PAH) concentration levels. The data, referred to the annual season, indicate that, near high traffic road, the above compounds are always present in the concentration level analytically detectable and that the concentration of benzo(a)pyrene is 2.7 ng/m 3 . The reported study is an useful instruments both for a road town planning, in order to people disease prevention, and for monitoring the evolution of PAH concentration levels in the future [it

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

    DEFF Research Database (Denmark)

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

    2013-01-01

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

  6. Study of the processes of ion pairs formation by the method of ion-ion coincidence: I2 and chlorine-containing hydrocarbons

    International Nuclear Information System (INIS)

    Golovin, A.V.

    1991-01-01

    A method of ion-ion coincidences was suggested to study the process of ion pairs formation during molecule photoionization. The principle of action of ion-ion coincidence method is based on recording of only the negative and positive ions that formed as a result of a molecule decomposition. The flowsheet of the facility of ion-ion coincidences was presented. The processes of ion pairs formation in iodine, chloroform, propyl-, n-propenyl-, tert.butyl- and benzyl-chlorides were studied. A simple model permitting to evaluate the dependence of quantum yield of ion pair formation on excitation energy was suggested

  7. The hydrogen concentration as parameter to identify natural attenuation processes of volatile chlorinated hydrocarbons in ground water; Die Wasserstoffkonzentration als Parameter zur Identifizierung des natuerlichen Abbaus von leichtfluechtigen Chlorkohlenwasserstoffen (LCKW) im Grundwasser

    Energy Technology Data Exchange (ETDEWEB)

    Alter, M.D.

    2006-06-15

    In this study, the hydrogen concentration as parameter to identify natural attenuation processes of volatile chlorinated hydrocarbons was investigated. The currently accepted and recommended bubble strip method for hydrogen sampling was optimized, and a storage method for hydrogen samples was developed. Furthermore batch experiments with a dechlorinating mixed culture and pure cultures were carried out to study H{sub 2}-concentrations of competing redox processes. The extraction of hydrogen from ground water was optimized by a reduced inlet diameter of the usually applied gas sampling bulbs, allowing a maximal turbulent ow and gas transfer. With a gas volume of 10 ml and flow rates of 50 to 140 ml/min, the course of extraction almost followed the theoretical course of equilibration. At flow rates > 100 ml/min a equilibrium of 98% was achieved within 20 min. Until recently it was generally accepted that hydrogen samples can be stored only for 2 hours and therefore have to be analyzed immediately in the eld. Here, it was shown that eld samples can be stored for 1-3 days until analysis. For the dechlorination of tetrachloroethene (PCE), a hydrogen threshold concentration of 1-2 nM was found with the dechlorinating mixed culture as well as with a pure culture of Sulfurospirillum multivorans in combination with another pure culture Methanosarcina mazei. No dechlorination was detectable below this concentration. With the dechlorinating mixed culture, this finding is valid for all successive dechlorination steps until ethene. The hydrogen threshold concentration for denitrification were below the detection limit of 0,2 nM with the dechlorinating mixed culture. A threshold concentration of 3,1-3,5 nM was found for sulphate reduction and a threshold of 7-9 nM H{sub 2} for hydrogenotrophic methanogenesis. This implies that the natural dechlorination at contaminated sites is preferred to competing processes like sulphate reduction and methanogenesis. The threshold

  8. Re-evaluation of solid-phase adsorption and desorption techniques for isolation of trace organic pollutants from chlorinated water.

    Science.gov (United States)

    Onodera, S; Nagatsuka, A; Rokuhara, T; Asakura, T; Hirayama, N; Suzuki, S

    1993-07-16

    Amberlite XAD resin and activated carbon columns were tested for their abilities to concentrate trace organic pollutants in chlorinated water. Both XAD-2 and XAD-7 resin columns (20 ml) were capable of adsorbing about 30% of total organic halogen (TOX) present in 20 l of drinking water (pH 7) containing about 100 micrograms/l of TOX, whereas the carbon column (10 ml) adsorbed over 90% of TOX. The adsorption capacity of XAD-7 resin was found to be strongly dependent on the solution pH, as compared with those of XAD-2 and carbon adsorbents. Soxhlet and sonication extractions were also evaluated for their abilities to recover the adsorbed organics from the adsorbents, by measurements of TOX, chromatographable compounds and mutagenicity in the eluates. Soxhlet extraction gave higher recoveries than sonication, as measured with the above indices, but these differences were generally small (ca. 20%), with exception of the carbon extracts. The XAD-2 and XAD-7 extracts of drinking water also showed about 3-4 times higher mutagenic activity than the carbon extracts.

  9. Chlorine isotope investigation of natural attenuation of trichloroethene in an aerobic aquifer

    International Nuclear Information System (INIS)

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

    1998-01-01

    Natural attenuation of chlorinated aliphatic hydrocarbons (CAHs) can be an important mechanism for groundwater remediation. It is difficult to determine the effectiveness of natural CAH attenuation from chemical analyses of groundwater samples because mixing, dispersion, and secondary reactions can mask the chemical evidence of attenuation. In this paper, the authors explore the application of stable chlorine isotope ratio measurements as a new tool for evaluating natural attenuation of CAHs. They report stable isotope ratios of chlorine in both trichloroethene (TCE) and inorganic chloride in groundwater from an aerobic aquifer beneath an extensively contaminated industrial site, the Paducah Gaseous Diffusion Plant in western Kentucky. Variations in the concentrations and chlorine isotope ratios of TCE and chloride in the groundwater are consistent with those expected from natural attenuation. These data support a model in which partial TCE degradation occurred in relatively impermeable, clay-rich sediments above the aquifer, and little or no further degradation of TCE occurred within the aquifer. A record of changing conditions within the TCE source area can be inferred from the spatial variation of chlorine isotope ratios for TCE and chloride within the plume

  10. On the efficiency of the hybrid and the exact second-order sampling formulations of the EnKF: a reality-inspired 3-D test case for estimating biodegradation rates of chlorinated hydrocarbons at the port of Rotterdam

    KAUST Repository

    El Gharamti, Mohamad; Valstar, Johan; Janssen, Gijs; Marsman, Annemieke; Hoteit, Ibrahim

    2016-01-01

    This study considers the assimilation problem of subsurface contaminants at the port of Rotterdam in the Netherlands. It involves the estimation of solute concentrations and biodegradation rates of four different chlorinated solvents. We focus

  11. On chlorinated hydrocarbons in the Indian Ocean

    Digital Repository Service at National Institute of Oceanography (India)

    Sarkar, A.; SenGupta, R.

    concentrations are due to larger anthropogenic inputs from the East Coast of India. The metabolite DDE constituted the major fraction of t-DDT in the fishes from the Arabian Sea suggesting that this region is not subject to high inputs of DDT...

  12. DNA-damage effect of polycyclic aromatic hydrocarbons from urban area, evaluated in lung fibroblast cultures

    International Nuclear Information System (INIS)

    Calesso Teixeira, Elba; Pra, Daniel; Idalgo, Daniele; Henriques, João Antonio Pêgas; Wiegand, Flavio

    2012-01-01

    This study was designed to biomonitor the effect of PAH extracts from urban areas on the DNA of lung cell cultures. The analyses of the polycyclic aromatic hydrocarbons (PAHs) were performed in atmospheric PM 2.5 and PM 10 collected at three sampling sites with heavy traffic located in the Metropolitan Area of Porto Alegre (MAPA) (Brazil). The concentrations of 16 major PAHs were determined according to EPA. Comet assay on V79 hamster lung cells was chosen for genotoxicity evaluation. Temperature, humidity, and wind speed were recorded. With regard to the damage index, higher levels were reported in the extract of particulate matter samples from the MAPA during the summer. High molecular weight compounds showed correlation with DNA damage frequency and their respective carcinogenicity. - Highlights: ► Cell line V79 was used to assess the effect of PAHs in PM 2.5 and PM 10 from urban area. ► Temperature showed a significant seasonal variation with the level of DNA damage. ► PAHs with higher molecular weight contributed to higher DNA damage levels. - DNA-damage effect of polycyclic aromatic hydrocarbons from urban area, showed difference according to season

  13. Chlorine in the stratosphere

    OpenAIRE

    VON CLARMANN, T.

    2013-01-01

    This paper reviews the various aspects of chlorine compounds in the stratosphere, both their roles as reactants and as tracers of dynamical processes. In the stratosphere, reactive chlorine is released from chlorofluorocarbons and other chlorine-containing organic source gases. To a large extent reactive chlorine is then sequestered in reservoir species ClONO2 and HCl. Re-activation of chlorine happens predominantly in polar winter vortices by heterogeneous reaction in combination with sunlig...

  14. Evaluation of current operating standards for chlorine dioxide in disinfection of dump tank and flume for fresh tomatoes.

    Science.gov (United States)

    Tomás-Callejas, Alejandro; López-Velasco, Gabriela; Valadez, Angela M; Sbodio, Adrian; Artés-Hernández, Francisco; Danyluk, Michelle D; Suslow, Trevor V

    2012-02-01

    Standard postharvest unit operations that rely on copious water contact, such as fruit unloading and washing, approach the criteria for a true critical control point in fresh tomato production. Performance data for approved sanitizers that reflect commercial systems are needed to set standards for audit compliance. This study was conducted to evaluate the efficacy of chlorine dioxide (ClO(2)) for water disinfection as an objective assessment of recent industry-adopted standards for dump tank and flume management in fresh tomato packing operations. On-site assessments were conducted during eight temporally distinct shifts in two Florida packinghouses and one California packinghouse. Microbiological analyses of incoming and washed fruit and dump and flume system water were evaluated. Water temperature, pH, turbidity, conductivity, and oxidation-reduction potential (ORP) were monitored. Reduction in populations of mesophilic and coliform bacteria on fruit was not significant, and populations were significantly higher (P Turbidity and conductivity increased with loads of incoming tomatoes. Water temperature varied during daily operations, but pH and ORP mostly remained constant. The industry standard positive temperature differential of 5.5°C between water and fruit pulp was not maintained in tanks during the full daily operation. ORP values were significantly higher in the flume than in the dump tank. A positive correlation was found between ORP and temperature, and negative correlations were found between ORP and turbidity, total mesophilic bacteria, and coliforms. This study provides in-plant data indicating that ClO(2) can be an effective sanitizer in flume and spray-wash systems, but current operational limitations restrict its performance in dump tanks. Under current conditions, ClO(2) alone is unlikely to allow the fresh tomato industry to meet its microbiological quality goals under typical commercial conditions.

  15. Toxicity evaluation of chlorinated organic compounds using immortalized rat hepatocytes; Fushika rat kansaibo wo mochiita yuki enso kagobutsu no dokusei hyoka no kokoromi

    Energy Technology Data Exchange (ETDEWEB)

    Sone, H; Nakajima, M; Yonemoto, J [National Institute for Environmental Studies, Tsukuba (Japan)

    1997-11-10

    Chlorinated organic compounds has high priority for toxicity screening among environmental hazardous chemicals. In the present study, we used immortalized rat hepatocytes as a liver model in vitro to evaluate the toxicity of nine chlorinated organic compounds. Toxicity of nine chlorinated organic compounds were evaluated to cellular viability of immortalized rat hapatocytes. The potency of the toxicity based on 50% inhibitory concentration (IC50) value was in the following order: triclocalban>triclosan>3,4-dichloroaniline>2,5-diclorophenol> 2,5-dichloroanisole>p-dichlorobenzene> p-chloroaniline>o-dichlorobenzene=tris (2-chloroethyl) phosphate. The rank order of cytotoxic potency of nine chemicals was compared with toxicity information using animals. The rank order of cytotoxic potency did not relative to the order referenced mean lethal dose (LD50) as an index of acute toxicity of rats or mice. However, the rank order of cytotoxic potency relatively correlated non-observed adverse effect level (NOAEL) under the exposure duration adjusted for chronic toxicity in vivo. These data suggests that the origin of testing cell had better to make match target organ of toxic chemicals for extrapolation from data of bioassay in vitro to in vivo. 16 refs., 2 figs., 3 tabs.

  16. Formation of secondary products in water purification. ; Toxicological evaluation of mutagenic chlorination by-products during drinking water treatment. Josui shori ni okeru fukuseiseibutsu. ; Josui shori ni okeru hen'i genseibusshitsu no dokusei hyoka

    Energy Technology Data Exchange (ETDEWEB)

    Nakamuro, K [Setsunan Univ., Osaka (Japan). Faculty of Pharmaceutical Sciences; Sayato, Y [Setsunan Univ., Osaka (Japan)

    1993-12-10

    The biological effects of acute toxicity, chronic toxicity, carcinogenicity, etc. of chlorination by-products detected in drinking water in Japan are discussed. The biological effects of representative chlorination by-products such as trihalomethane, haloacetic acid, haloaldehyde, haloacetonitrile, chlorophenol, chloropicrin, etc. as well as the evaluation of mutagenicity in drinking water purification process, for which Ames Salmonella/microsome assay is used for safety evaluation of drinking water, are discussed. The extent of the contribution of mutagenicity of chlorination disinfection by-products to the mutagenicity of drinking water is investigated. It must be admitted that biological evaluation of the safety of water quality is impossible currently by using only the known chemical substances contained in drinking water. The effects of chlorination and ozone treatment which are often applied to drinking water treatment are different each other. 58 refs., 1 fig., 4 tabs.

  17. An in vitro evaluation of the antibacterial efficacy of chlorine dioxide on E. faecalis in bovine incisors.

    Science.gov (United States)

    Eddy, Russell S; Joyce, Anthony P; Roberts, Steven; Buxton, Thomas B; Liewehr, Frederick

    2005-09-01

    This study investigated the ability of chlorine dioxide to eliminate Enterococcus faecalis from dentinal tubules of bovine incisors. Thirty-seven extracted bovine incisor roots were sectioned into seventy-four 5 mm disks. Standardized lumens were filled with either sterile Brain Heart Infusion Broth (contamination controls, n = 10) or BHI containing E. faecalis (1.0 x 10 cfu/ml). Disks were incubated in 5% CO2 at 37 degrees C for 72 h. To simulate endodontic instrumentation the lumens were again enlarged. Sixty disks were randomly divided into four experimental groups and filled with one of the following irrigants: 10% Clidox-S (chlorine dioxide), 13.8% BioClenz (chlorine dioxide), 5.25% Clorox, or saline. The disks were incubated for 30 min and were then frozen, pulverized, serially diluted in phosphate buffered saline, and plated on BHI plates in triplicate. Total colony forming units were counted macroscopically. Statistical analysis of the data was performed with a Kruskal-Wallis one-way ANOVA on ranks (p " denotes significant differences): Saline > Clidox-S = BioClenz > Clorox. All negative controls were sterile. Chlorine dioxide and NaOCL were both effective in eliminating E. faecalis from the dentinal disks within 30 min.

  18. Evaluation of perchlorate sources in the Rialto-Colton and Chino California subbasins using chlorine and oxygen isotope ratio analysis

    Science.gov (United States)

    Hatzinger, Paul B.; Böhlke, John Karl; Izbicki, John; Teague, Nicholas F.; Sturchio, Neil C.

    2015-01-01

    Perchlorate (ClO4-) in groundwater can be from synthetic or natural sources, the latter of which include both historical application of imported nitrate fertilizers from the Atacama Desert of Chile and naturally deposited ClO4- that forms atmospherically and accumulates in arid regions such as the southwestern US. The objective of this study was to evaluate the use of isotopic data to distinguish sources of ClO4- in groundwater in a specific region of the Rialto-Colton and Chino, CA groundwater subbasins (Study Area). This region includes two groundwater ClO4- plumes emanating from known military/industrial source areas, and a larger area outside of these plumes having measurable ClO4-. Perchlorate extracted from wells in this region was analyzed for chlorine and oxygen stable isotope ratios (δ37Cl, δ18O, δ17O) and radioactive chlorine-36 (36Cl) isotopic abundance, along with other geochemical, isotopic, and hydrogeologic data. Isotope data indicate synthetic, Atacama, and indigenous natural ClO4- were present in the Study Area. Stable isotope data from nearly all sampled wells within the contours of the two characterized plumes, including those located in a perched zone and within the regional groundwater aquifer, were consistent with a dominant synthetic ClO4- source. In wells downgradient from the synthetic plumes and in the Chino subbasin to the southwest, isotopic data indicate the dominant source of ClO4- largely was Atacama, presumably from historical application of nitrate fertilizer in this region. Past agricultural land use and historical records are consistent with this source being present in groundwater. The 36Cl and δ18O data indicate that wells having predominantly synthetic or Atacama ClO4- also commonly contained small fractions of indigenous natural ClO4-. The indigenous ClO4- was most evident isotopically in wells having the lowest overall ClO4- concentrations (< 1 μg/L), consistent with its occurrence as a low-level background constituent

  19. Evaluation of abundant hydrocarbon-generation depressions in the deepwater area of Qiongdongnan Basin, South China Sea

    Institute of Scientific and Technical Information of China (English)

    LIU Zhen; SUN Zhipeng; WANG Zisong; ZHANG Wei; LI Tingan; HE Weijun; LI Fengxia

    2016-01-01

    It has been confirmed that the key source rocks of Qiongdongnan Basin are associated with the Yacheng Formation, which was deposited in a transitional marine-continental environment. Because the distribution and evolution patterns of the source rocks in the major depressions are different, it is important to determine the most abundant hydrocarbon-generation depressions in terms of exploration effectiveness. Based on an analysis of organic matter characteristics of the source rocks, in combination with drilling data and seismic data, this paper establishes a model to evaluate the hydrocarbon-generation depressions in the deepwater area of Qiongdongnan Basin. First of all, by using the method of seismic-facies model analysis, the distribution of sedimentary facies was determined. Then, the sedimentary facies were correlated with the organic facies, and the distribution of organic facies was predicted. Meanwhile, the thickness of source rocks for all the depressions was calculated on the basis of a quantitative analysis of seismic velocity and lithology. The relationship between mudstone porosity and vitrinite reflectance (Ro) was used to predict the maturity of source rocks. Second, using the parameters such as thickness and maturity of source rocks, the quantity and intensity of gas generation for Yacheng and Lingshui Formations were calculated. Finally, in combination with the identified hydrocarbon resources, the quantity and intensity of gas generation were used as a guide to establish an evaluation standard for hydrocarbon-generation depressions, which was optimized for the main depressions in the Central Depression Belt. It is proposed that Lingshui, Ledong, Baodao and Changchang Depressions are the most abundant hydrocarbon depressions, whilst Songnan and Beijiao Depressions are rich hydrocarbon depressions. Such an evaluation procedure is beneficial to the next stage of exploration in the deep-water area of Qiongdongnan Basin.

  20. Model studies for evaluating the acute neurobehavioral effects of complex hydrocarbon solvents. I. Validation of methods with ethanol

    NARCIS (Netherlands)

    McKee, R.H.; Lammers, J.H.C.M.; Hoogendijk, E.M.G.; Emmen, H.H.; Muijser, H.; Barsotti, D.A.; Owen, D.E.; Kulig, B.M.

    2006-01-01

    As a preliminary step to evaluating the acute neurobehavioral effects of hydrocarbon solvents and to establish a working model for extrapolating animal test data to humans, joint neurobehavioral/toxicokinetic studies were conducted which involved administering ethanol to rats and volunteers. The

  1. Effectiveness of Chlorinated Water, Sodium Hypochlorite, Sodium ...

    African Journals Online (AJOL)

    This study evaluated the efficacy of chlorinated water, sodium hypochlorite solution, sodium chloride solution and sterile distilled water in eliminating pathogenic bacteria on the surfaces of raw vegetables. Lettuce vegetables were dipped in different concentrations of chlorinated water, sodium hypochlorite solution, sodium ...

  2. Evaluation of phytoremediation of petroleum hydrocarbon and heavy metals with using Catharanthus roseus

    Directory of Open Access Journals (Sweden)

    Mehri Askary Mehrabadi

    2014-08-01

    Full Text Available Crude oil pollution is an inevitable worldwide phenomenon in oil producing and consuming areas that stems from human error, accidental discharge and other sources. The aim of this study was to evaluate the phytoremediation potential of vinca in petroleum-polluted soil. The experiment was laid out as a completely randomized design in 3 replications with different concentrations of crude oil (0, 0.5, 1, 2, 3 and 4 % V/W in pot planting stage. At the end of the 70-day period, soil samples were analyzed for total hydrocarbons removal. Contents of pb, zn and Ni were measured by atomic absorption from the soils and the leaves. Statistical analysis of data were performed on the basis of duncan’s test and by using of SPSS16 software. In concentrations higher than 3 % no growth was observed. The growth parameters such as stem length, stem fresh and dry matter decreased progressively from 0.5-3 % crude oil in soil. The results showed heavy metal accumulation in plant leaves and reduction of them in the soil. Heavy metals containing zinc, lead and nickel in plant increased in different concentration of crude oil. Total hydrocarbons and heavy metals containing zinc, lead and nickel reduced were in planted contaminated soil. This study showed that Periwinkle was able to grow and survive in low concentrations of oil and reduced pollutants in the soil. Based upon these results, Catharanthus roseus can be used as phytoremediator of petroleum-contaminated soil in low concentrations.

  3. Development of an analysis method for determining chlorinated hydrocarbons in marine sediments and suspended matter giving particular consideration to supercritical fluid extraction; Entwicklung eines Analysenverfahrens zur Bestimmung von chlorierten Kohlenwasserstoffen in marinen Sedimenten und Schwebstoffen unter besonderer Beruecksichtigung der ueberkritischen Fluidextraktion

    Energy Technology Data Exchange (ETDEWEB)

    Sterzenbach, D.

    1997-11-01

    The purpose of the present study was to develop an analysis method for chlorinate hydrocarbons in marine environments using supercritical fluid extraction (SFE) instead of conventional approaches. In order to apply this extraction method the available SFE device had to be extended and all the individual steps of the analysis method had to be optimised and adapted. As chlorinated hydrocarbons only occur at very low concentrations in marine environments (ppm to ppt range) the analysis method had to be extremely sensitive. High sensitivity, in town, is generally associated with a high susceptibility of an analysis method to faults through contamination or losses. This meant that the entire method and all its individual steps had to scrutinised for such weak points and improved where necessary. A method for sampling suspended matter in marine environments had to be developed which permits efficient separation of the smallest possible particles from seawater. The designated purpose of the developed analysis method is to deal with topical aspects of marine chemistry relating to sources, transport, distribution, and the fate of chlorinated hydrocarbons in marine environments. (orig.) [Deutsch] Ziel der vorliegenden Arbeit ist, ein Analysenverfahren fuer chlorierte Kohlenwasserstoffe in der marinen Umwelt zu entwickeln. Dabei soll die ueberkritische Fluidextraktion (SFE) anstelle herkoemmlicher Verfahren eingesetzt werden. Fuer die Anwendung dieser Extraktionsmethode ist es erforderlich, das zur Verfuegung stehende SFE-Geraet zu erweitern und saemtliche Teilschritte des Analysenverfahrens zu optimieren und auf diese Methode abzustimmen. Der Umstand, dass die chlorierten Kohlenwasserstoffe nur in sehr geringen Konzentrationen in der marinen Umwelt vorkommen (ppm- bis ppt-Bereich), erfordert eine sehr hohe Empfindlichkeit des Analysenverfahrens. Eine hohe Empfindlichkeit bedingt eine grosse Stoeranfaelligkeit des Analysenverfahrens durch Kontaminationen oder Verluste. Aus

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

    International Nuclear Information System (INIS)

    Garrett, W.E. Jr.; Laylor, M.M.

    1995-01-01

    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

  5. Heat-Activated Persulfate Oxidation of Chlorinated Solvents in Sandy Soil

    Directory of Open Access Journals (Sweden)

    Jialu Liu

    2014-01-01

    Full Text Available Heat-activated persulfate oxidative treatment of chlorinated organic solvents containing chlorinated ethenes and ethanes in soil was investigated with different persulfate dosages (20 g/L, 40 g/L, and 60 g/L and different temperatures (30°C, 40°C, and 50°C. Chlorinated organic solvents removal was increased as persulfate concentration increase. The persulfate dosage of 20 g/L with the highest OE (oxidant efficiency value was economically suitable for chlorinated organic solvents removal. The increasing temperature contributed to the increasing depletion of chlorinated organic solvents. Chlorinated ethenes were more easily removed than chlorinated ethanes. Moreover, the persulfate depletion followed the pseudo-first-order reaction kinetics (kps=0.0292 [PS]0+0.0008, R2=0.9771. Heat-activated persulfate appeared to be an effective oxidant for treatment of chlorinated hydrocarbons.

  6. Evaluation of total petroleum hydrocarbons (TPH in urban soil from Maicao, Colombia

    Directory of Open Access Journals (Sweden)

    Martha L. Castellanos

    2015-09-01

    Full Text Available The presence of total petroleum hydrocarbons (TPH and their effects on soil properties in urban area of Maicao, Colombia, was evaluated. 18 sites were selected: nine contaminated and nine non-contaminated and two depths (0-30 cm and 30-60 cm were evaluated. The medium TPH fraction (Soxhlet reflux method, EPA 3540C and heavy TPH fraction (Soxhlet reflux method, EPA 3550C were extracted. TPH were identified by gas chromatography with flame ionization detector (GC-FID. Soil parameters related potential adsorption were determined: pH, electrical conductivity (EC, organic carbon (OC, cation exchange capacity (CEC, texture; soil moisture retention, aggregate stability. High contents of TPH was found in all fractions. No significant changes were found for texture and (EC. There was an increase in the content of OC (500%, soil aggregation and aggregate stability (200%; slight decrease pH, CEC and soil moisture retention (23.5% soil surface. These results show the vulnerability of the urban soils to the TPH contamination and exposure of the human population to these contaminants.

  7. Durability and degradation analysis of hydrocarbon ionomer membranes in polymer electrolyte fuel cells accelerated stress evaluation

    Science.gov (United States)

    Shimizu, Ryo; Tsuji, Junichi; Sato, Nobuyuki; Takano, Jun; Itami, Shunsuke; Kusakabe, Masato; Miyatake, Kenji; Iiyama, Akihiro; Uchida, Makoto

    2017-11-01

    The chemical durabilities of two proton-conducting hydrocarbon polymer electrolyte membranes, sulfonated benzophenone poly(arylene ether ketone) (SPK) semiblock copolymer and sulfonated phenylene poly(arylene ether ketone) (SPP) semiblock copolymer are evaluated under accelerated open circuit voltage (OCV) conditions in a polymer electrolyte fuel cell (PEFC). Post-test characterization of the membrane electrodes assemblies (MEAs) is carried out via gel permeation chromatography (GPC) and nuclear magnetic resonance (NMR) spectroscopy. These results are compared with those of the initial MEAs. The SPP cell shows the highest OCV at 1000 h, and, in the post-test analysis, the SPP membrane retains up to 80% of the original molecular weight, based on the GPC results, and 90% of the hydrophilic structure, based on the NMR results. The hydrophilic structure of the SPP membrane is more stable after the durability evaluation than that of the SPK. From these results, the SPP membrane, with its simple hydrophilic structure, which does not include ketone groups, is seen to be significantly more resistant to radical attack. This structure leads to high chemical durability and thus impedes the chemical decomposition of the membrane.

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

    Directory of Open Access Journals (Sweden)

    Alexandra Huttinger

    2015-10-01

    Full Text Available 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.

  9. Microbial transformation of chlorinated aromatics in sediments

    OpenAIRE

    Beurskens, J.E.M.

    1995-01-01

    Numerous contaminants like heavy metals, polycyclic aromatic hydrocarbons (PAHs), chlorinated benzenes (CBs), polychlorinated biphenyls (PCBs), polychlorinated dibenzo- p -dioxins (PCDDs) and polychlorinated furans (PCDFs) are detected in the major rivers in the Netherlands. These contaminants have relatively low aqueous solubilities and bind substantially to the suspended solids in river water. Due to decreasing stream velocities in the downstream stretches of a...

  10. Behavior of chlorine in lake water

    International Nuclear Information System (INIS)

    Sriraman, A.K.

    2006-01-01

    Water from monsoon fed Sagre lake is being used as a source of raw water for Tarapur Atomic Power Station (TAPS--1 and 2). The raw water from the lake is initially pumped to Sagre water treatment plant (SWTP) operated by Maharashtra Industrial Development Corporation (MIDC) from where, the processed water is sent to cater the needs of both the units of TAPS-1 and 2, townships of TAPS and MIDC, and the nearby villages. At the SWTP the raw water is treated with alum to remove the turbidity, filtered and chlorinated using bleaching powder. All these years the raw water is chlorinated in such a way whereby a residual chlorine level of 0.5-1.0 mg/l, is maintained at the outlet of water treatment plant. The adequacy of the current chlorination practice was investigated, at the request of the NPC-500 MWe group during 1990, so that the future requirements of raw water for TAPP-3 and 4, can be met from the expanded SWTP. In this connection experiments on chlorine dose -- residual chlorine relationship and the decay pattern of chlorine with time was carried out in the lake water (with low value of total dissolved solids and total hardness 3 sample at the site. The total bacterial count in the raw water observed to be 10 7 counts/ml originally came down to 10 3 counts/ml at the end of one-hour exposure time to chlorine. It was found that the chlorine demand of the water was around 6 mg/l. In addition Jar test to evaluate the aluminum dose was also carried out. Based on these experiments a chlorine dose of 6 mg/l for one hour contact time was arrived at. The experimental findings were in agreement with the current chlorination practices. (author)

  11. Halogenated hydrocarbons - an environmental problem

    Energy Technology Data Exchange (ETDEWEB)

    Schoeler, H F; Thofern, E

    1984-01-01

    The paper provides a survey of the incidence of highly volatile halogenated hydrocarbons in ground, surface and drinking water as well as in the snows of Western Germany. Almost the entire production of chlorinated solvents is released into the environment. The absorption media are mostly soil, water and atmosphere. Whereas in the atmosphere elimination reactions take place, solvents that have passed the soil get into the ground water owing to their persistence and can cause considerable pollutions of drinking water. Moreover haloforms may occur in drinking water, which are produced during chlorine disinfection of pre-treated water.

  12. Evaluation of clean-up agents for total petroleum hydrocarbon analysis in biota and sediments.

    NARCIS (Netherlands)

    Muijs, B.; Jonker, M.T.O.

    2009-01-01

    Petroleum hydrocarbons (oil) are common environmental contaminants. For risk assessment purposes, their concentrations in environmental matrixes, such as biota and soils/sediments are frequently determined by solvent extraction and subsequent analysis with gas chromatography (GC) equipped with flame

  13. Technology assessment: Chlorine chemistry

    International Nuclear Information System (INIS)

    Wolff, H.; Alwast, H.; Buttgereit, R.

    1994-01-01

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

  14. Evaluating the utility of hydrocarbons for Re-Os geochronology : establishing the timing of processes in petroleum ore systems

    Energy Technology Data Exchange (ETDEWEB)

    Selby, D.; Creaser, R.A. [Alberta Univ., Edmonton, AB (Canada). Dept. of Earth and Atmospheric Sciences

    2005-07-01

    Oil from 6 Alberta oil sands deposits were analyzed with a rhenium-osmium (Re-Os) isotope chronometer, an emerging tool for determining valuable age information on the timing of petroleum generation and migration. The tool uses molybdenite and other sulphide minerals to establish the timing and duration of mineralization. However, establishing the timing events of petroleum systems can be problematic because viable sulphides for the Re-Os chronometer are often not available. Therefore, the known presence of Re and Os associated with organic matter in black shale, a common source of hydrocarbons, may suggest that bitumen and petroleum common to petroleum systems may be utilised for Re-Os geochronology. This study evaluated the potential of the Re-Os isotopic system for geochronology and as an isotopic tracer for hydrocarbon systems. The evaluation was based on Re-Os isotopic analyses of bitumen and oil sands. Hydrocarbons formed from migrated oil in both Alberta oil sand deposits and a Paleozoic Mississippi Valley-type lead-zinc deposit contain significant Re and Os contents with high {sup 187}Re/{sup 188}Os and radiogenic {sup 187}Os/{sup 188}Os ratios suitable for geochronology. The oil from the 6 Alberta oil sand deposits yields Re-Os analyses with very high Re/{sup 188}Os ratios, and radiogenic Os isotopic compositions. Regression of the Re-Os data yields a date of 116 {+-} 27 Ma. This date plausibly represents the period of in situ radiogenic growth of {sup 187}Os following hydrocarbon migration and reservoir filling. Therefore, directly dating these processes, and this formation age corresponds with recent burial history models for parts of the Western Canada Sedimentary Basin. The very high initial {sup 187}Os/{sup 188}Os for this regression requires rocks much older than Cretaceous for the hydrocarbon source.

  15. Evaluating Evidence for Association of Human Bladder Cancer with Drinking-Water Chlorination Disinfection By-Products.

    Science.gov (United States)

    Hrudey, Steve E; Backer, Lorraine C; Humpage, Andrew R; Krasner, Stuart W; Michaud, Dominique S; Moore, Lee E; Singer, Philip C; Stanford, Benjamin D

    2015-01-01

    Exposure to chlorination disinfection by-products (CxDBPs) is prevalent in populations using chlorination-based methods to disinfect public water supplies. Multifaceted research has been directed for decades to identify, characterize, and understand the toxicology of these compounds, control and minimize their formation, and conduct epidemiologic studies related to exposure. Urinary bladder cancer has been the health risk most consistently associated with CxDBPs in epidemiologic studies. An international workshop was held to (1) discuss the qualitative strengths and limitations that inform the association between bladder cancer and CxDBPs in the context of possible causation, (2) identify knowledge gaps for this topic in relation to chlorine/chloramine-based disinfection practice(s) in the United States, and (3) assess the evidence for informing risk management. Epidemiological evidence linking exposures to CxDBPs in drinking water to human bladder cancer risk provides insight into causality. However, because of imprecise, inaccurate, or incomplete estimation of CxDBPs levels in epidemiologic studies, translation from hazard identification directly to risk management and regulatory policy for CxDBPs can be challenging. Quantitative risk estimates derived from toxicological risk assessment for CxDBPs currently cannot be reconciled with those from epidemiologic studies, notwithstanding the complexities involved, making regulatory interpretation difficult. Evidence presented here has both strengths and limitations that require additional studies to resolve and improve the understanding of exposure response relationships. Replication of epidemiologic findings in independent populations with further elaboration of exposure assessment is needed to strengthen the knowledge base needed to better inform effective regulatory approaches.

  16. Evaluation of thirteen haloacetic acids and ten trihalomethanes formation by peracetic acid and chlorine drinking water disinfection.

    Science.gov (United States)

    Xue, Runmiao; Shi, Honglan; Ma, Yinfa; Yang, John; Hua, Bin; Inniss, Enos C; Adams, Craig D; Eichholz, Todd

    2017-12-01

    Free chlorine is a commonly used disinfectant in drinking water treatment. However, disinfection by-products (DBPs) are formed during water disinfection. Haloacetic acids (HAAs) and trihalomethanes (THMs) are two major groups of DBPs. Iodo-HAAs and iodo-THMs (I-HAAs and I-THMs) are formed during the disinfection of the water containing high levels of iodide and are much more toxic than their chlorinated and brominated analogs. Peracetic acid (PAA) is a strong antimicrobial disinfectant that is expected to reduce the formation of HAAs and THMs during disinfection. In this study, the formations of thirteen HAAs and ten THMs, including the iodinated forms, have been investigated during PAA disinfection and chlorination as the comparison. The DBP formations under different iodide concentrations, pHs, and contact times were systematically investigated. Two types of commercial PAAs containing different concentrations of PAA and hydrogen peroxide (H 2 O 2 ) were studied. A solid-phase microextraction gas chromatography-mass spectrometry method was upgraded for THM analysis including I-THMs. HAAs were analyzed by following a recently developed high performance ion chromatography-tandem mass spectrometry method. Results show that the ratio of PAA and H 2 O 2 concentration significantly affect the formation of I-THMs and I-HAAs. During PAA disinfection with lower PAA than H 2 O 2 , no detectable levels of THMs and HAAs were observed. During PAA disinfection with higher PAA than H 2 O 2 , low levels of monoiodoacetic acid, diiodoacetic acid, and iodoform were formed, and these levels were enhanced with the increase of iodide concentration. No significant quantities of chloro- or bromo-THMs and HAAs were formed during PAA disinfection treatment. Copyright © 2017 Elsevier Ltd. All rights reserved.

  17. Evaluating Evidence for Association of Human Bladder Cancer with Drinking-Water Chlorination Disinfection By-Products

    Science.gov (United States)

    Hrudey, Steve E.; Backer, Lorraine C.; Humpage, Andrew R.; Krasner, Stuart W.; Michaud, Dominique S.; Moore, Lee E.; Singer, Philip C.; Stanford, Benjamin D.

    2015-01-01

    Exposure to chlorination disinfection by-products (CxDBPs) is prevalent in populations using chlorination-based methods to disinfect public water supplies. Multifaceted research has been directed for decades to identify, characterize, and understand the toxicology of these compounds, control and minimize their formation, and conduct epidemiologic studies related to exposure. Urinary bladder cancer has been the health risk most consistently associated with CxDBPs in epidemiologic studies. An international workshop was held to (1) discuss the qualitative strengths and limitations that inform the association between bladder cancer and CxDBPs in the context of possible causation, (2) identify knowledge gaps for this topic in relation to chlorine/chloramine-based disinfection practice(s) in the United States, and (3) assess the evidence for informing risk management. Epidemiological evidence linking exposures to CxDBPs in drinking water to human bladder cancer risk provides insight into causality. However, because of imprecise, inaccurate, or incomplete estimation of CxDBPs levels in epidemiologic studies, translation from hazard identification directly to risk management and regulatory policy for CxDBPs can be challenging. Quantitative risk estimates derived from toxicological risk assessment for CxDBPs currently cannot be reconciled with those from epidemiologic studies, notwithstanding the complexities involved, making regulatory interpretation difficult. Evidence presented here has both strengths and limitations that require additional studies to resolve and improve the understanding of exposure response relationships. Replication of epidemiologic findings in independent populations with further elaboration of exposure assessment is needed to strengthen the knowledge base needed to better inform effective regulatory approaches. PMID:26309063

  18. Third-Party Evaluation of Petro Tex Hydrocarbons, LLC, ReGen Lubricating Oil Re-refining Process

    Energy Technology Data Exchange (ETDEWEB)

    Compere, A L [ORNL; Griffith, William {Bill} L [ORNL

    2009-04-01

    This report presents an assessment of market, energy impact, and utility of the PetroTex Hydrocarbons, LLC., ReGen process for re-refining used lubricating oil to produce Group I, II, and III base oils, diesel fuel, and asphalt. PetroTex Hydrocarbons, LLC., has performed extensive pilot scale evaluations, computer simulations, and market studies of this process and is presently evaluating construction of a 23 million gallon per year industrial-scale plant. PetroTex has obtained a 30 acre site in the Texas Industries RailPark in Midlothian Texas. The environmental and civil engineering assessments of the site are completed, and the company has been granted a special use permit from the City of Midlothian and air emissions permits for the Texas Commission on Environmental Quality.

  19. Aromatic hydrocarbons

    International Nuclear Information System (INIS)

    Roder, M.

    1985-01-01

    Papers dealing with radiolysis of aromatic hydrocarbons of different composition (from benzene to terphenyls and hydrocarbons with condensed rings) as well as their mixtures (with alkanes, alkenes, other aromatic hydrocarbons) are reviewed. High radiation stability of aromatic hydrocarbons in condensed phases associated with peculiarities of molecular structure of compounds is underlined. Mechanisms of radiolytic processes, vaues of product yields are considered

  20. Evaluation of Perchlorate Sources in the Rialto-Colton and Chino California Subbasins using Chlorine and Oxygen Isotope Ratio Analysis

    Science.gov (United States)

    2015-03-01

    matches, air bags , chlorine bleach, safety flares, perchloric acid, and chlorate herbicides (Trumpholt et al., 2005; Aziz et al., 2006, 2008). Based...L, assuming no losses to biodegradation or other removal processes. Additional information on Atacama NO3- fertilizers as a source of ClO4- can be...in each well), the IX columns were removed from the each well, sealed in Zip-Loc type bags , placed at 4oC (or on ice), and shipped to the UIC EIGL

  1. Evaluation of metals and hydrocarbons in sediments from a tropical tidal flat estuary of Southern Brazil

    International Nuclear Information System (INIS)

    Costa, Eduardo S.; Grilo, Caroline F.; Wolff, George A.; Thompson, Anu; Figueira, Rubens Cesar Lopes; Neto, Renato Rodrigues

    2015-01-01

    Highlights: • Metals and hydrocarbons in estuary mouth showed indication of anthropogenic input. • Metals in estuary mouth were associated with petroleum-derivative hydrocarbons. • Metals were possibly associated with activities that use oil and its derivatives. • Copper was associated with domestic sewage. - Abstract: Although the Passagem Channel estuary, Espírito Santo State, Brazil, is located in an urbanized and industrialized region, it has a large mangrove system. Here we examined natural and anthropogenic inputs that may influence trace metal (Cd, Cr, Cu, Ni, Sc, Pb and Zn) and hydrocarbon (n-alkane and terpane) deposition in three sediment cores collected in the tidal flat zone of the estuary. The cores were also analyzed for carbonate, grain size and stable isotopic composition (δ 13 C org. and δ 15 N total ). Metal enrichment and its association to petroleum hydrocarbons in the surficial sediments of one of the cores, indicate crude oil and derivative inputs, possibly from small vessels and road run-off from local heavy automobile traffic. At the landward sites, the major contributions for metals and hydrocarbons are from natural sources, but in one case, Cu may have been enriched by domestic effluent inputs

  2. Comparative evaluation of antiplaque and antigingivitis effects of an herbal and chlorine dioxide mouthwashes: A clinicomicrobiological study

    Directory of Open Access Journals (Sweden)

    Srinivasa T Siddeshappa

    2018-01-01

    Full Text Available Aim: The aim of the present study was to compare the efficacy of herbal mouthwash and chlorine dioxide mouthwash in reduction of plaque and gingivitis. Settings and Design: In a randomized clinical trial, forty patients were randomly selected and divided equally into two groups. Materials and Methods: After professional oral prophylaxis, the clinical parameters plaque index, gingival index, and modified sulcular bleeding index were recorded at baseline, 7th day, 14th day, and 21st day. The plaque samples were collected from gingival sulcus with an absorbent sterile paper point and were stored in a thioglycollate broth, then sent for microbiological examination. The microbial colony-forming units were assessed at baseline, 7th day, 14th day, and 21st day for Streptococcus mutans, Tannerella forsythia, and Fusobacterium nucleatum. Results: There was a statistical significant reduction in both clinical and microbiological parameters were observed with use of both the mouthwashes. However, herbal mouthwash was more effective in reducing the plaque and gingivitis than chlorine dioxide mouthwash. Conclusion: Herbal mouthwash was statistically efficacious in controlling plaque and gingivitis with potent antimicrobial activity.

  3. Tolerance of anaerobic bacteria to chlorinated solvents.

    Science.gov (United States)

    Koenig, Joanna C; Groissmeier, Kathrin D; Manefield, Mike J

    2014-01-01

    The aim of this research was to evaluate the effects of four chlorinated aliphatic hydrocarbons (CAHs), perchloroethene (PCE), carbon tetrachloride (CT), chloroform (CF) and 1,2-dichloroethane (1,2-DCA), on the growth of eight anaerobic bacteria: four fermentative species (Escherichia coli, Klebsiella sp., Clostridium sp. and Paenibacillus sp.) and four respiring species (Pseudomonas aeruginosa, Geobacter sulfurreducens, Shewanella oneidensis and Desulfovibrio vulgaris). Effective concentrations of solvents which inhibited growth rates by 50% (EC50) were determined. The octanol-water partition coefficient or log Po/w of a CAH proved a generally satisfactory measure of its toxicity. Most species tolerated approximately 3-fold and 10-fold higher concentrations of the two relatively more polar CAHs CF and 1,2-DCA, respectively, than the two relatively less polar compounds PCE and CT. EC50 values correlated well with growth rates observed in solvent-free cultures, with fast-growing organisms displaying higher tolerance levels. Overall, fermentative bacteria were more tolerant to CAHs than respiring species, with iron- and sulfate-reducing bacteria in particular appearing highly sensitive to CAHs. These data extend the current understanding of the impact of CAHs on a range of anaerobic bacteria, which will benefit the field of bioremediation.

  4. Evaluation of the performance of biochars as an adsorbent for polycyclic aromatic hydrocarbons

    Science.gov (United States)

    Jung, J.; Kang, S.; Ok, Y.; Choi, Y.

    2016-12-01

    Biochars, byproducts generated by pyrolysis of biomass, are known to have several advantages as a soil amendment such as carbon sequestration effect, enhancement of soil microbial activity, and nutrient supply. Because of their high surface area and affinity to organic pollutants, biochars are also being evaluated as an adsorbent for hydrophobic organic pollutants such as polycyclic aromatic hydrocarbons (PAHs) in soils, stormwater, and wastewater. Depending on their organic precursors and pyrolysis temperatures, biochars have been shown to have various physicochemical properties, which should determine their performance as an adsorbent for hydrophobic organic pollutants. In this study, we obtained biochars derived from soybean stover, wood chip, rice husk, and sewage sludge with pyrolysis temperatures of 700°, 250°, 500°, and 500°, respectively, to investigate their performance for PAH adsorption. Adsorption kinetic and isotherm experiments were conducted using naphthalene and phenanthrene as model compounds. Soybean stover biochar reached close to equilibrium in 7 days while the others did in 25 days in the kinetic experiments. The first-order sorption rate constants were greater for naphthalene than for phenanthrene for all biochars studied, and they were generally in the order of soybean stover>rice husk>sewage sludge>wood chip biochars for the two contaminants. The removal rates of aqueous PAHs at equilibrium were in the order of soybean stover>rice husk>sewage sludge>wood chip biochars at a concentration range of a few ng/mL. The results suggested that the sorption capability and the rate is generally greater for biochar produced from plant materials than that from sludge, and for biochar produced at higher pyrolysis temperature. Comparing the sorption properties of the biochars and granular activated carbon (GAC), it is shown that biochar produced at optimal conditions can exhibit performance for PAH adsorption similar to GAC.

  5. Alternative methods for chlorination

    Energy Technology Data Exchange (ETDEWEB)

    Fiessinger, F; Rook, J J; Duguet, J P

    1985-12-01

    Existing disinfectants are oxidative agents which all present negative effects on subsequent treatment processes. None of them has decisive advantages over chlorine, although chlorine-dioxide and chloramines might at times be preferable. Optimum treatment practices will improve the removal of organic precursors before final disinfection which could then consist in a light chlorine addition. A philosophy of radical change in water treatment technology encompassing physical treatment without chemicals such as membrane filtration, solid disinfectants is presented.

  6. Chlorination and chloramines formation

    International Nuclear Information System (INIS)

    Yee, Lim Fang; Mohd Pauzi Abdullah; Sadia Ata; Abbas Abdullah; Basar IShak; Khairul Nidzham

    2008-01-01

    Chlorination is the most important method of disinfection in Malaysia which aims at ensuring an acceptable and safe drinking water quality. The dosing of chlorine to surface water containing ammonia and nitrogen compounds may form chloramines in the treated water. During this reaction, inorganic and organic chloramines are formed. The recommended maximum acceptable concentration (MAC) for chloramines in drinking water is 3000 μg/L. The production of monochloramine, dichloramine and trichloramine is highly dependent upon pH, contact time and the chlorine to ammonia molar ratio. The purpose of this study is to examine the formation of chloramines that occur upon the chlorination during the treatment process. Chloramines were determined using the N,N-diethyl-p-phenylenediamine (DPD) colorimetric method. The influences of ammonia, pH and chlorine dosage on the chloramines formation were also studied. This paper presents a modeling approach based on regression analysis which is designed to estimate the formation of chloramines. The correlation between the concentration of chloramines and the ammonia, pH and chlorine dosage was examined. In all cases, the quantity of chloramines formed depended linearly upon the amount of chlorine dosage. On the basis of this study it reveals that the concentration of chloramines is a function of chlorine dosage and the ammonia concentration to the chlorination process. PH seems to not significantly affect the formation of chloramines. (author)

  7. The role of chlorine and additives of PVC-plastic in combustion

    International Nuclear Information System (INIS)

    Mattila, H.

    1991-01-01

    The PVC differs from other common plastics due to the chlorine content. As the PVC is combusted, the chlorine is released mainly as hydrogen chloride. The content of chlorinated hydrocarbons is small, but these can also contain polychlorinated dibenzofuranes and dibenzodioxines, which are extremely poisonous. The aim of this study was to find out, what is the portion of PVC combustion in total emission of chlorinated hydrocarbons. Additionally, the amounts chlorine coming into combustion process with ordinary fuels have been estimated, and they are compared with the amounts of PVC. The chloride content of municipal wastes vary in between 0.4-0.9 %. The portion of plastics is about 30 % of the total, and the rest being from paper, food , wood and garden wastes an textiles. Both organic and inorganic chlorine form gaseous hydrogen chlorid in combustion processes. HCl can then react with oxygen and produce caseous chlorine. This can react with unreacted carbon of the smoke and produce different kinds of chlorinated hydrocarbons. The portion of PVC of the chlorine going into combustion in Finland has been estimated to be about 1-2 %. Combustion tests were made using coal and bark and plastic waste as additional fuel. It was noticed that addition of plastic decreased the amount of polyaromatic hydrocarbons in the smoke. Chlorinated dioxins and furans occurred a little less in the gases of combustion of plastic mixtures not containing PVC than in reference tests, but they increased when PVC containing plastic mixture was combusted, but more chlorinated dioxins and furans were absorbed into fly ash, so the emissions remained almost the same

  8. Aerobic biodegradation of a mixture of chlorinated organics in ...

    African Journals Online (AJOL)

    STORAGESEVER

    2008-07-04

    Jul 4, 2008 ... DCM; and 0.232 – 0.588 week-1 for DCA in both water microcosms with higher degradation generally observed in New ... Key words: Bioaugmentation, biodegradation, biostimulation, chlorinated aliphatic hydrocarbons, microcosms. ... culture (OD of 1 at λ600) of the consortia was added separately to.

  9. Evaluation of the effectiveness of different methods for the remediation of contaminated groundwater by determining the petroleum hydrocarbon content

    Energy Technology Data Exchange (ETDEWEB)

    Voyevoda, Maryna; Geyer, Wolfgang; Mothes, Sibylle [Department of Analytical Chemistry, UFZ, Helmholtz Centre for Environmental Research - UFZ, Leipzig (Germany); Mosig, Peter [Centre for Environmental Biotechnology, UFZ, Helmholtz Centre for Environmental Research - UFZ, Leipzig (Germany); Seeger, Eva M. [Department of Environmental Biotechnology, UFZ, Helmholtz Centre for Environmental Research - UFZ, Leipzig (Germany)

    2012-08-15

    The effectiveness of different remediation procedures for decreasing the amount of TPH (total petroleum hydrocarbons) in contaminated groundwater was evaluated at the site of a former refinery. The investigations were carried out on samples taken from several gravel based HSSF (horizontal subsurface flow) constructed wetlands (CW) which differed in relation to their filter material additives (no additive, charcoal, and ferric oxides additives) and examined the potential effect of these additives on the overall treatment efficiency. Samples of the following gravel based HSSF CW were investigated. No filter additive (system A), 0.1% activated carbon (system B), 0.5% iron(III) hydroxide (system C), and the reference (system D). Systems A-C were planted with common reed (Phragmites australis), whereas system D remained unplanted. In addition, the influence of seasonal conditions on the reduction of these hydrocarbons and the correlation between the amounts of TPH and BTEX (benzene, toluene, ethylbenzene, and xylene isomers), on the one hand, and methyl tert-butyl ether, on the other, was investigated. The study was carried out by using a modified GC-FID approach and multivariate methods. The investigations carried out in the first year of operation demonstrated that the effectiveness of the petroleum hydrocarbon removal was highest and reached a level of 93 {+-} 3.5% when HSSF filters with activated carbon as a filter additive were used. This remediation method allowed the petroleum hydrocarbon content to be reduced independently of seasonal conditions. The correlation between the reduction of TPH and BTEX was found to be R = 0.8824. Using this correlation coefficient, the time-consuming determination of the BTEX content was no longer necessary. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  10. Chlorine solar neutrino experiment

    International Nuclear Information System (INIS)

    Rowley, J.K.; Cleveland, B.T.; Davis, R. Jr.

    1984-01-01

    The chlorine solar neutrino experiment in the Homestake Gold Mine is described and the results obtained with the chlorine detector over the last fourteen years are summarized and discussed. Background processes producing 37 Ar and the question of the constancy of the production rate of 37 Ar are given special emphasis

  11. Tightness and suitability evaluation of abandoned salt caverns served as hydrocarbon energies storage under adverse geological conditions (AGC)

    International Nuclear Information System (INIS)

    Wei, Liu; Jie, Chen; Deyi, Jiang; Xilin, Shi; Yinping, Li; Daemen, J.J.K.; Chunhe, Yang

    2016-01-01

    Highlights: • Tightness conditions are set to assess use of old caverns for hydrocarbons storage. • Gas seepage and tightness around caverns are numerically simulated under AGC. • κ of interlayers act as a key factor to affect the tightness and use of salt cavern. • The threshold upper permeability of interlayers is proposed for storing oil and gas. • Three types of real application are introduced by using the tightness conditions. - Abstract: In China, the storage of hydrocarbon energies is extremely insufficient partially due to the lack of storage space, but on the other side the existence of a large number of abandoned salt caverns poses a serious threat to safety and geological environments. Some of these caverns, defined as abandoned caverns under adverse geological conditions (AGC), are expected to store hydrocarbon energies (natural gas or crude oil) to reduce the risk of potential disasters and simultaneously support the national strategic energy reserve of China. Herein, a series of investigations primarily related to the tightness and suitability of the caverns under AGC is performed. Laboratory measurements to determine the physical and mechanical properties as well as porosity and permeability of bedded salt cores from a near target cavern are implemented to determine the petro-mechanical properties and basic parameters for further study. The results show that the mechanical properties of the bedded rock salts are satisfactory for the stability of caverns. The interface between the salt and interlayers exhibits mechanical properties that are between those of rock salt and interlayers and in particular is not a weak zone. The silty mudstone interlayers have relatively high porosity and permeability, likely due to their low content of clay minerals and the presence of halite-filled cracks. The conditions for evaluating the tightness and suitability of a cavern for storing hydrocarbons are proposed, including “No tensile stress,”

  12. Toxicity of jet fuel aliphatic and aromatic hydrocarbon mixtures on human epidermal Keratinocytes: evaluation based on in vitro cytotoxicity and interleukin-8 release

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Jen-Hung (Chung-Shan Medical University Hospital, Department of Dermatology, Taichung, Taiwan, R.O.C); Lee, Chia-Hue; Tsang, Chau-Loong [National Chung-Hsing University, College of Veterinary Medicine, Taichung (Taiwan); Monteiro-Riviere, Nancy A.; Riviere, Jim E. [North Carolina State University, Center for Chemical Toxicology Research and Pharmacokinetics (CCTRP), Raleigh, NC (United States); Chou, Chi-Chung [National Chung-Hsing University, College of Veterinary Medicine, Taichung (Taiwan); National Chung-Hsing University, College of Veterinary Medicine, Taichung (Taiwan)

    2006-08-15

    Jet fuels are complex mixtures of aliphatic (ALI) and aromatic (ARO) hydrocarbons that vary significantly in individual cytotoxicity and proinflammatory activity in human epidermal keratinocytes (HEK). In order to delineate the toxicological interactions among individual hydrocarbons in a mixture and their contributions to cutaneous toxicity, nine ALI and five ARO hydrocarbons were each divided into five (high/medium/low cytotoxic and strong/weak IL-8 induction) groups and intra/inter-mixed to assess for their mixture effects on HEK mortality and IL-8 release. Addition of single hydrocarbon to JP-8 fuel was also evaluated for their changes in fuel dermatotoxicity. The results indicated that when hydrocarbons were mixed, HEK mortality and IL-8 release were not all predictable by their individual ability affecting these two parameters. The lowest HEK mortality (7%) and the highest IL-8 production were induced with mixtures including high cytotoxic and weak IL-8 inductive ARO hydrocarbons. Antagonistic reactions not consistently correlated with ALI carbon chain length and ARO structure were evident and carried different weight in the overall mixture toxicities. Single addition of benzene, toluene, xylene or ethylbenzene for up to tenfold in JP-8 did not increase HEK mortality while single addition of ALI hydrocarbons exhibited dose-related differential response in IL-8. In an all ALI environment, no single hydrocarbon is the dominating factor in the determination of HEK cytotoxicity while deletion of hexadecane resulted in a 2.5-fold increase in IL-8 production. Overall, decane, undecane and dodecane were the major hydrocarbons associated with high cytotoxicity while tetradecane, pentadecane and hexadecane were those which had the greatest buffering effect attenuating dermatotoxicity. The mixture effects must be considered when evaluating jet fuel toxicity to HEK. (orig.)

  13. Relation between chlorine with the quality of crude water

    International Nuclear Information System (INIS)

    Lim, Fang Yee; Mohd Pauzi Abdullah

    2008-01-01

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

  14. Oil spill aftermath : temporal evaluation of hydrocarbon sources in Guanabara Bay, Brazil

    International Nuclear Information System (INIS)

    Meniconi, M.F.G.; Massone, C.G.; Scofield, A.L.; Junior, V.J.F.

    2005-01-01

    The sources of polycyclic aromatic hydrocarbons (PAH) in environmental ecosystems are both natural and anthropogenic. PAHs interact with different types of environmental compartments and are subject to processes that lead to geochemical fates such as physical-chemical transformation, biodegradation and photo-oxidation. This study examined the sources of PAHs in the estuarine sediment of Guanabara Bay, Brazil following an accidental oil spill from an oil refinery in January 2000. The main portion of the oil was carried by tidal currents and wind. It spread over the water and reached islands and shorelines at the north part of the bay. The objective of this study was to determine the likely sources of hydrocarbons in the bay where untreated municipal sewage and industrial wastes are also dumped. Sediment samples were collected using cores and dredges from the intertidal and subtidal regions of the bay, reflecting both affected and unaffected areas. This paper summarized the results of 16 EPA priority PAH and their alkylated homologues from 21 sediment samples collected in the bay 10 days after the oil spill, immediately after the clean up effort, and then 3 years later. The hydrocarbon source was determined using PAH ratios for the samples studied. The highest PAH concentration was observed in 2000 as a result of the petrogenic and pyrolytic contribution to the sediments. 38 refs., 3 tabs., 9 figs

  15. Evaluation of the condensation potential of hydrocarbon fluids in the national gas pipeline system; establishing of adequate operational schemes

    International Nuclear Information System (INIS)

    Pineda Gomez, Cesar Augusto; Arenas Mantilla, Oscar Armando; Santos Santos, Nicolas

    2007-01-01

    For transporting industry of natural gas by pipeline systems, it's vital to guarantee the integrity of their lines, in order to decrease operational costs and prevent accidents that may damaging against people's safety, the environment or the infrastructure itself. in this paper it's presented the principal compounds from o technical study about principal net and its distribution branches to municipalities of the National System Transport of Natural Gas pointed by the Colombian Natural Gas Company - ECOGAS, (specifically the Cusiana - Porvenir - La Belleza, La Belleza - Cogua, La Belleza - Vasconia, Vasconia - Neiva and Vasconia - Cali gas lines, (see Figure 1). The principal objective is evaluate the possible condensation of hydrocarbons fluids inside gas lines, due to compositional characteristics of the gas, the different topographical conditions along the gas line route and the actual and future operational conditions to be implemented in the system. The evaluation performed over this gas streams, generates transcendental information in the creation of safe operational limits that minimizing the existence of obstacle problems and damages over pipeline systems and process equipment, due to the presence of liquid hydrocarbons inside these flow lines. This article has been prepared in four sections in order to guarantee easy access to each one of the steps involved in the study. Section one presents the compositional and thermodynamic analysis of feeding gas streams; in section two, its presented the required information for modeling gas lines with definition of the gas pipeline numerical simulation model in stable state; section three presents the sensitivity analysis for gas variation upon loading gas composition at the inlet point of the system, variation of the operational conditions (flow, pressure and gas temperature) and environment temperatures for the different inlet points (branches) with verification of compliance of the Unique Transport Regulation

  16. Study for the chlorination of zirconium oxide

    International Nuclear Information System (INIS)

    Seo, E.S.M.; Takiishi, H.; Paschoal, J.O.A.; Andreoli, M.

    1990-12-01

    In the development of new ceramic and metallic materials the chlorination process constitutes step in the formation of several intermediate compounds, such as metallic chlorides, used for the production of high, purity raw materials. Chlorination studies with the aim of fabrication special zirconium-base alloys have been carried out at IPEN. Within this program the chlorination technique has been used for zirconium tetrachloride production from zirconium oxide. In this paper some relevant parameters such as: time and temperature of reaction, flow rate of chloride gas and percentage of the reducing agent which influence the efficiency of chlorination of zirconium oxide are evaluated. Thermodynamical aspects about the reactions involved in the process are also presented. (author)

  17. Evaluation of the Removal of Hydrocarbons from Soil Media Using Persulfate Oxidation in the Presence of Mineral Siderite

    Directory of Open Access Journals (Sweden)

    Farzad Mohammadi

    2016-09-01

    Full Text Available Introduction and purpose: Soil contamination by petroleum is mostly resulted from oil exploration, refining processes, leaking of oil products from storage tanks, leaking from pipelines due to pipe friction and decay, refinery wastewater discharge and agricultural irrigation with such materials. Sodium persulfate (Na2S2O8, which is a chemical oxidant, could be activated in the presence of ferrous (Fe2+ and, leading to the treatment of a wide range of soil contaminants. Therefore, this study aimed to evaluate the removal of hydrocarbons from soil media using persulfate oxidation in the presence of mineral siderite. Methods: Initially, oil-contaminated soil was prepared in the form of two separate samples, including silt-clay and sandy-loam soils, which were orderly spiked with 5000 mg fuel oil per kilogram of dry soil. Following that, the effects of various factors, such as different concentrations of persulfate (100-500 mmol/L and siderite (0.1-0.5 g/L, pH (3-9 and temperature (20-60◦C and the removal of petroleum hydrocarbon were assessed.Results: In this study, the optimum condition for degeneration of total petroleum hydrocarbon in silt-clay soils was reported, as follows: temperature: 60◦C, pH: 3, and persulfate/siderite molar ratio of 400 mmol/L to 4.0 g/L. Meanwhile, the optimum condition for the removal of hydrocarbon from sandy-loam soils was pH: 3, temperature: 60◦C and persulfate/siderite molar ratio of 300 mmol/L to 3.0 g/L.Conclusion: According to the results of this study, the optimal amount of persulfate and siderite could be used to remove hydrocarbons from contaminated soils.

  18. Evaluation of a novel and efficient solvent system containing chlorinated cobalt dicarbollide for radio-cesium recovery from acidic wastes

    Energy Technology Data Exchange (ETDEWEB)

    Kandwal, Pankaj; Mohapatra, Prasanta Kumar [Bhabha Atomic Research Centre, Mumbai (India). Radiochemistry Div.

    2014-11-01

    A novel solvent system containing chlorinated cobalt dicarbollide (CCD) in a diluent mixture containing 2-nitrophenyloctyl ether (NPOE) and n-dodecane was found to be highly efficient for the extraction of radio-cesium from acidic feed conditions. When PEG-400 (polyethylene glycol with average molecular weight of 400) was added to the solvent system, it was found to extract radio-strontium as well similar to that reported with the UNEX (Universal Extractant) solvent. The solvent system was found to be superior as compared to analogous solvent systems reported previously using CCD in either nitrobenzene or PTMS (phenyltrifluoromethyl sulphone, a fluorinated diluent). The present work deals with less toxic solvent formulation which can be used as an alternative to these hazardous/toxic chemicals for simultaneous recovery of Cs(I) and Sr(II) from acidic solutions. Batch co-current extraction data are also presented for the simultaneous recovery of Cs and Sr which indicated near quantitative extraction (>99.5%) of the metal ions in 4 and 3 stages, respectively. The reusability and radiolytic stability studies were also carried out which suggested highly encouraging results.

  19. Evaluation of the fate and transport of chlorinated ethenes in a complex groundwater system discharging to a stream in Wonju, Korea

    Science.gov (United States)

    Lee, Seong-Sun; Kaown, Dugin; Lee, Kang-Kun

    2015-11-01

    Chlorinated ethenes such as trichloroethylene (TCE) are common and persistent groundwater contaminants. If contaminated groundwater discharges to a stream, then stream water pollution near the contamination site also becomes a problem. In this respect, the fate and transport of chlorinated ethenes around a stream in an industrial complex were evaluated using the concentration of each component, and hydrogeochemical, microbial, and compound-specific carbon isotope data. Temporal and spatial monitoring reveal that a TCE plume originating from main and local source zones continues to be discharged to a stream. Groundwater geochemical data indicate that aerobic conditions prevail in the upgradient area of the studied aquifer, whereas conditions become anaerobic in the downgradient. The TCE molar fraction is high at the main and local source zones, ranging from 87.4 to 99.2% of the total volatile organic compounds (VOCs). An increasing trend in the molar fraction of cis-1, 2-Dichloroethene (cis-DCE) and vinyl chloride (VC) was observed in the downgradient zone of the study area. The enriched δ13C values of TCE and depleted values of cis-DCE in the stream zone, compared to those of the source zone, also suggest biodegradation of VOCs. Microbial community structures in monitoring wells adjacent to the stream zone in the downgradient area were analyzed using 16S rRNA gene-based pyrosequencing to identify the microorganisms responsible for biodegradation. This was attributed to the high relative abundance of dechlorinating bacteria in monitoring wells under anaerobic conditions farthest from the stream in the downgradient area. The multilateral approaches adopted in this study, combining hydrogeochemical and biomolecular methods with compound-specific analyses, indicate that contaminants around the stream were naturally attenuated by active anaerobic biotransformation processes.

  20. Evaluation of the fate and transport of chlorinated ethenes in a complex groundwater system discharging to a stream in Wonju, Korea.

    Science.gov (United States)

    Lee, Seong-Sun; Kaown, Dugin; Lee, Kang-Kun

    2015-11-01

    Chlorinated ethenes such as trichloroethylene (TCE) are common and persistent groundwater contaminants. If contaminated groundwater discharges to a stream, then stream water pollution near the contamination site also becomes a problem. In this respect, the fate and transport of chlorinated ethenes around a stream in an industrial complex were evaluated using the concentration of each component, and hydrogeochemical, microbial, and compound-specific carbon isotope data. Temporal and spatial monitoring reveal that a TCE plume originating from main and local source zones continues to be discharged to a stream. Groundwater geochemical data indicate that aerobic conditions prevail in the upgradient area of the studied aquifer, whereas conditions become anaerobic in the downgradient. The TCE molar fraction is high at the main and local source zones, ranging from 87.4 to 99.2% of the total volatile organic compounds (VOCs). An increasing trend in the molar fraction of cis-1, 2-Dichloroethene (cis-DCE) and vinyl chloride (VC) was observed in the downgradient zone of the study area. The enriched δ(13)C values of TCE and depleted values of cis-DCE in the stream zone, compared to those of the source zone, also suggest biodegradation of VOCs. Microbial community structures in monitoring wells adjacent to the stream zone in the downgradient area were analyzed using 16S rRNA gene-based pyrosequencing to identify the microorganisms responsible for biodegradation. This was attributed to the high relative abundance of dechlorinating bacteria in monitoring wells under anaerobic conditions farthest from the stream in the downgradient area. The multilateral approaches adopted in this study, combining hydrogeochemical and biomolecular methods with compound-specific analyses, indicate that contaminants around the stream were naturally attenuated by active anaerobic biotransformation processes. Copyright © 2015 Elsevier B.V. All rights reserved.

  1. Chlorinated drinking water for lightweight laying hens

    Directory of Open Access Journals (Sweden)

    A.F. Schneider

    Full Text Available ABSTRACT The study aimed to evaluate the effect of different levels of chlorine in drinking water of laying hens on zootechnical performance, eggs shell quality, hemogasometry levels and calcium content in tibia. 144 Hy-Line laying hens, 61 weeks old, were used distributed in 24 metabolism cages. They were subjected to water diets, for a period of 28 days, using sodium hypochlorite as a chlorine source in order to obtain the following concentrations: 5ppm (control, 20ppm, 50ppm, and 100ppm. Their performance was evaluated through water consumption, feed intake, egg production and weight, egg mass, feed conversion. Shell quality was measured by specific gravity. At the end of the experiment, arterial blood was collected for blood gas level assessment and a poultry of each replicate was sacrificed to obtain tibia and calcium content measurement. There was a water consumption reduction from 20ppm of chlorine and feed intake reduction in poultry receiving water with 100ppm of chlorine. The regression analysis showed that the higher the level of chlorine in water, the higher the reduction in consumption. There were no differences in egg production and weight, egg mass, feed conversion, specific gravity, tibia calcium content, and hemogasometry levels (hydrogenionic potential, carbon dioxide partial pressure, oxygen partial pressure, sodium, potassium, chloride, bicarbonate, carbon dioxide total concentration, anion gap and oxygen saturation. The use of levels above 5ppm of chlorine is not recommended in the water of lightweight laying hens.

  2. CHARACTERIZATION OF ENALAPRIL AND RANITIDINE CHLORINATION BY-PRODUCTS BY LIQUID CHROMATOGRAPHY/HIGH-RESOLUTION MASS SPECTROMETRY AND THEIR TOXICITY EVALUATION

    Directory of Open Access Journals (Sweden)

    Frederico Jehár Oliveira Quintão

    Full Text Available Due to its low cost, its capability for disinfection and oxidation, chlorination using gaseous chlorine or hypochlorite salts, has also been commonly applied in water treatment plants for oxidation and disinfection purposes. Little is known about the identity and toxicity of by-products resulting from the chlorination of pharmaceutical micropollutants, such as enalapril (ENA and ranitidine (RAN. ENA and RAN chlorination by-products were characterized in this study by high-performance liquid chromatography coupled to high-resolution mass spectrometry (HPLC/HRMS and their toxicity were assessed by MTT assay. Chlorination experiments with ENA and RAN solutions (10 mg L-1 indicate degradation efficiencies of 100% for both compounds after only 5 min of exposure to chlorine at concentration of 9.53 mg Cl2 L-1. On the other hand mineralization rates were lower than 3%, thereby indicating there was accumulation of degradation by-products in all experiments. Mass spectrometric analysis revealed, at all times of reaction after the addition of hypochlorite, the presence of 1-(2-((4-(chlorophenyl-1-ethoxy-1-oxobutan-2-ylaminopropanoylpyrrolidine-2-carboxylic acid (enalapril by-product and N-chloro-N-(2-(((chloro-5-((dimethylaminomethylfuran-2-ylmethylsulfinylethyl-N-methyl-2-nitroethene 1,1-diamine (ranitidine by-product. Despite the formation of oxidized chlorinated by-products in all chlorination assays, the treated solutions were nontoxic to HepG2 cells by the MTT assay. It has been observed that chlorination (10 mg L-1, 5 min of ENA and RAN solutions exhibited high degradation efficiencies of the target compounds and low mineralization rates. Based on the mass spectrometry data, the routes for ENA and RAN successive oxidation by chlorine has been proposed.

  3. Evaluation of mineral oil saturated hydrocarbons (MOSH and mineral oil aromatic hydrocarbons (MOAH in pure mineral hydrocarbon-based cosmetics and cosmetic raw materials using 1H NMR spectroscopy [version 2; referees: 3 approved

    Directory of Open Access Journals (Sweden)

    Dirk W. Lachenmeier

    2017-08-01

    Full Text Available Mineral hydrocarbons consist of two fractions, mineral oil saturated hydrocarbons (MOSH and mineral oil aromatic hydrocarbons (MOAH. MOAH is a potential public health hazard because it may include carcinogenic polycyclic compounds. In the present study, 400 MHz nuclear magnetic resonance (NMR spectroscopy was introduced, in the context of official controls, to measure MOSH and MOAH in raw materials or pure mineral hydrocarbon final products (cosmetics and medicinal products. Quantitative determination (qNMR has been established using the ERETIC methodology (electronic reference to access in vivo concentrations based on the PULCON principle (pulse length based concentration determination. Various mineral hydrocarbons (e.g., white oils, paraffins or petroleum jelly were dissolved in deuterated chloroform. The ERETIC factor was established using a quantification reference sample containing ethylbenzene and tetrachloronitrobenzene. The following spectral regions were integrated: MOSH δ 3.0 – 0.2 ppm and MOAH δ 9.2 - 6.5, excluding solvent signals. Validation showed a sufficient precision of the method with a coefficient of variation <6% and a limit of detection <0.1 g/100 g. The applicability of the method was proven by analysing 27 authentic samples with MOSH and MOAH contents in the range of 90-109 g/100 g and 0.02-1.10 g/100 g, respectively. It is important to distinguish this new NMR-approach from the hyphenated liquid chromatography-gas chromatography methodology previously used to characterize MOSH/MOAH amounts in cosmetic products. For mineral hydrocarbon raw materials or pure mineral hydrocarbon-based cosmetic products, NMR delivers higher specificity without any sample preparation besides dilution. Our sample survey shows that previous methods may have overestimated the MOAH amount in mineral oil products and opens new paths to characterize this fraction. Therefore, the developed method can be applied for routine monitoring of consumer

  4. An accurate evaluation of the potential hazardous impact of Polycyclic Aromatic Hydrocarbons in biochars

    Science.gov (United States)

    María De la Rosa, José; Sánchez-Martín, Águeda; Villaverde-Capellán, Jaime; Madrid, Fernando; Paneque, Marina; Knicker, Heike

    2017-04-01

    Biochar may act as a soil conditioner, enhancing plant growth by supplying and retaining nutrients and by providing other services such as improving soil physical, chemical and biological properties. Feedstock properties and production conditions drive the nature of produced biochars [1]. Special attention have to be paid to their content of polycyclic aromatic hydrocarbons (PAHs), which are persistent organic pollutants formed during biochar production due to incomplete combustion (pyrolysis step) [2]. These PAHs may enter the environment when the biochar is applied as soil conditioner. Therefore, the intention of this study was to test a potential hazardous impact of biochar amendment due to the presence of PAHs. In order to find a relationship between pyrolysis conditions, feedstock and abundance of PAHs, four biochars produced from different feedstock were analyzed. Three biochars were produced by technical pyrolysis (500-600 °C; 20 min) from wood, paper sludge and sewage sludge respectively (samples B1, B2 and B3). The fourth biochar sample derived from old grapevine wood by using the traditional carbonization method in kilns (kiln-stack wood biochar; B4). A detailed characterization of physical and chemical properties of these samples can be found in De la Rosa et al, [3]. Two different PAHs extraction techniques were applied to evaluate the total and available PAHs content of the biochars. They consisted in an extraction with toluene using a Soxhlet extractor and a non-exhaustive extraction with Cyclodextrins (CDs). Chromatographic and mass spectrometric conditions applied are described in [1]. Total PAHs yielded between 3 ppm (B3) and 7 (B4) ppm. The production of biochar by using traditional kilns instead of controlled pyrolysis, increased significantly the total PAHs levels. No direct relationship was found between the total PAHs and the PAHs extracted by CDs, which can be considered as the bioavailable fraction. This parameter should replace the total

  5. Oxidation of fluoroquinolone antibiotics and structurally related amines by chlorine dioxide: Reaction kinetics, product and pathway evaluation.

    Science.gov (United States)

    Wang, Pei; He, Yi-Liang; Huang, Ching-Hua

    2010-12-01

    Fluoroquinolones (FQs) are a group of widely prescribed antibiotics and have been frequently detected in the aquatic environment. The reaction kinetics and transformation of seven FQs (ciprofloxacin (CIP), enrofloxacin (ENR), norfloxacin (NOR), ofloxacin (OFL), lomefloxacin (LOM), pipemidic acid (PIP) and flumequine (FLU)) and three structurally related amines (1-phenylpiperazine (PP), N-phenylmorpholine (PM) and 4-phenylpiperidine (PD)) toward chlorine dioxide (ClO(2)) were investigated to elucidate the behavior of FQs during ClO(2) disinfection processes. The reaction kinetics are highly pH-dependent, can be well described by a second-order kinetic model incorporating speciation of FQs, and follow the trend of OFL > ENR > CIP ∼ NOR ∼ LOM > > PIP in reactivity. Comparison among FQs and related amines and product characterization indicate that FQs' piperazine ring is the primary reactive center toward ClO(2). ClO(2) likely attacks FQ's piperazinyl N4 atom followed by concerted fragmentation involving piperazinyl N1 atom, leading to dealkylation, hydroxylation and intramolecular ring closure at the piperazine moiety. While FQs with tertiary N4 react faster with ClO(2) than FQs with secondary N4, the overall reactivity of the piperazine moiety also depends strongly on the quinolone ring through electronic effects. The reaction rate constants obtained in clean water matrix can be used to model the decay of CIP by ClO(2) in surface water samples, but overestimate the decay in wastewater samples. Overall, transformation of FQs, particularly for those with tertiary N4 amines, could be expected under typical ClO(2) disinfection conditions. However, the transformation may not eliminate antibacterial activity because of little destruction at the quinolone ring. Copyright © 2010 Elsevier Ltd. All rights reserved.

  6. Sonolysis of chlorinated compounds in aqueous solution.

    Science.gov (United States)

    Lim, Myung Hee; Kim, Seung Hyun; Kim, Young Uk; Khim, Jeehyeong

    2007-02-01

    To examine the reaction rates of sonochemical degradation of aqueous phase carbon tetrachloride, trichloroethylene and 1,2,3-trichloropropane at various temperatures, power intensities, and saturating gases, the batch tests were carried out. The degradations of chlorinated hydrocarbons were analyzed as pseudo first order reactions and their reaction rate constants were in the range of 10(-1)-10(-3)/min. The reaction was fast at the low temperature with higher power intensity. Also, the reaction went fast with the saturating gas with high specific heat ratio, high solubility and low thermal conductivity. The main mechanism of destruction of chemicals was believed the thermal combustion in the bubble.

  7. An In Silico Approach for Evaluating a Fraction-Based, Risk Assessment Method for Total Petroleum Hydrocarbon Mixtures

    Directory of Open Access Journals (Sweden)

    Nina Ching Y. Wang

    2012-01-01

    Full Text Available Both the Massachusetts Department of Environmental Protection (MADEP and the Total Petroleum Hydrocarbon Criteria Working Group (TPHCWG developed fraction-based approaches for assessing human health risks posed by total petroleum hydrocarbon (TPH mixtures in the environment. Both organizations defined TPH fractions based on their expected environmental fate and by analytical chemical methods. They derived toxicity values for selected compounds within each fraction and used these as surrogates to assess hazard or risk of exposure to the whole fractions. Membership in a TPH fraction is generally defined by the number of carbon atoms in a compound and by a compound's equivalent carbon (EC number index, which can predict its environmental fate. Here, we systematically and objectively re-evaluate the assignment of TPH to specific fractions using comparative molecular field analysis and hierarchical clustering. The approach is transparent and reproducible, reducing inherent reliance on judgment when toxicity information is limited. Our evaluation of membership in these fractions is highly consistent (̃80% on average across various fractions with the empirical approach of MADEP and TPHCWG. Furthermore, the results support the general methodology of mixture risk assessment to assess both cancer and noncancer risk values after the application of fractionation.

  8. Evaluation of hydrocarbon-liquid disposition. Topical report, July 1990-November 1990

    International Nuclear Information System (INIS)

    Gibbs, J.E.; Tannehill, C.C.

    1991-08-01

    The report examines the current practice and technology used in natural gas liquids (NGL) extraction in small scale gas processing facilities. The removal of NGLs from a natural gas stream is driven by two factors: (1) hydrocarbon dew point and heating value control; and (2) economic recovery of the NGLs. Wellhead condensates are purchased at a price per barrel adjusted for transportation costs. Water is disposed of by truck at an approximate cost of $1.00 per barrel. Natural gas with a BTU content greater than 1150 normally will require NGL extraction prior to pipeline delivery. NGL recovery, if not required for hydrocarbon dew point or heating value control, must be justified by the value of the liquids exceeding the sum of the following costs: BTU value of the liquids; fuel consumed in the process; operating costs for the plant; and return of the plant investment capital. Liquids are purchased based on component posted prices with the cost of transportation, component fractionation and marketing subtracted. Rich gas in small quantities is normally processed in a straight refrigeration plant. Leaner gas in larger quantities is normally processed in a cryogenic expansion plant. With current technology, there is not sufficient margin to treat lean gases on a small scale

  9. Evaluation of a new battery of toxicity tests for boreal forest soils: assessment of the impact of hydrocarbons and salts.

    Science.gov (United States)

    Princz, Juliska I; Moody, Mary; Fraser, Christopher; Van der Vliet, Leana; Lemieux, Heather; Scroggins, Rick; Siciliano, Steven D

    2012-04-01

    The ability to assess the toxic potential of soil contamination within boreal regions is currently limited to test species representative of arable lands. This study evaluated the use of six boreal plant species (Pinus banksiana, Picea glauca, Picea mariana, Populus tremuloides, Calamagrostis Canadensis, and Solidago canadensis) and four invertebrate species (Dendrodrilus rubidus, Folsomia nivalis, Proisotoma minuta, and Oppia nitens) and compared their performance to a suite of standard agronomic soil test species using site soils impacted by petroleum hydrocarbon (PHC) and salt contamination. To maintain horizon-specific differences, individual soil horizons were collected from impacted sites and relayered within the test vessels. Use of the boreal species was directly applicable to the assessment of the contaminated forest soils and, in the case of the hydrocarbon-impacted soil, demonstrated greater overall sensitivity (25th percentile of estimated species sensitivity distribution [ESSD25] = 5.6% contamination: 10,600 mg/kg fraction 3 [F3; equivalent hydrocarbon range of >C16 to C34] Of/Oh horizon, and 270 mg/kg F3 Ahg horizon) relative to the standard test species (ESSD25 = 23% contamination: 44,000 mg/kg F3 Of/Oh horizon, and 1,100 mg/kg F3 Ahg horizon). For salinity, there was no difference between boreal and standard species with a combined ESSD25 = 2.3%, equating to 0.24 and 0.25 dS/m for the Ah and Ck horizons. The unequal distribution of soil invertebrates within the layered test vessels can confound test results and the interpretation of the toxic potential of a site. The use of test species relevant to boreal eco-zones strengthens the applicability of the data in support of realistic ecological risk assessments applicable to the boreal regions. Copyright © 2012 SETAC.

  10. Zirconia concentrate chlorination

    International Nuclear Information System (INIS)

    Costa, N.G.; Albuquerque Brocchi, E. de

    1990-01-01

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

  11. Chlorine trifluoride (1963)

    International Nuclear Information System (INIS)

    Vincent, L.M.; Gillardeau, J.

    1963-01-01

    This monograph on chlorine trifluoride may be considered as a working tool useful in gaseous diffusion research. It consists of data gathered from the literature and includes furthermore a certain amount of original data. This monograph groups together the physical, chemical and physiological properties of chlorine trifluoride, as well as the preparation and analytical methods. It has been thought wise to add some technological information, and the safety regulations governing its use. (authors) [fr

  12. Chlorine as a primary radical: evaluation of methods to understand its role in initiation of oxidative cycles

    Science.gov (United States)

    Young, C. J.; Washenfelder, R. A.; Edwards, P. M.; Parrish, D. D.; Gilman, J. B.; Kuster, W. C.; Mielke, L. H.; Osthoff, H. D.; Tsai, C.; Pikelnaya, O.; Stutz, J.; Veres, P. R.; Roberts, J. M.; Griffith, S.; Dusanter, S.; Stevens, P. S.; Flynn, J.; Grossberg, N.; Lefer, B.; Holloway, J. S.; Peischl, J.; Ryerson, T. B.; Atlas, E. L.; Blake, D. R.; Brown, S. S.

    2014-04-01

    The role of chlorine atoms (Cl) in atmospheric oxidation has been traditionally thought to be limited to the marine boundary layer, where they are produced through heterogeneous reactions involving sea salt. However, recent observation of photolytic Cl precursors (ClNO2 and Cl2) formed from anthropogenic pollution has expanded the potential importance of Cl to include coastal and continental urban areas. Measurements of ClNO2 in Los Angeles during CalNex (California Nexus - Research at the Nexus of Air Quality and Climate Change) showed it to be an important primary (first generation) radical source. Evolution of ratios of volatile organic compounds (VOCs) has been proposed as a method to quantify Cl oxidation, but we find no evidence from this approach for a significant role of Cl oxidation in Los Angeles. We use a box model with the Master Chemical Mechanism (MCM v3.2) chemistry scheme, constrained by observations in Los Angeles, to examine the Cl sensitivity of commonly used VOC ratios as a function of NOx and secondary radical production. Model results indicate VOC tracer ratios could not detect the influence of Cl unless the ratio of [OH] to [Cl] was less than 200 for at least a day. However, the model results also show that secondary (second generation) OH production resulting from Cl oxidation of VOCs is strongly influenced by NOx, and that this effect obscures the importance of Cl as a primary oxidant. Calculated concentrations of Cl showed a maximum in mid-morning due to a photolytic source from ClNO2 and loss primarily to reactions with VOCs. The [OH] to [Cl] ratio was below 200 for approximately 3 h in the morning, but Cl oxidation was not evident from the measured ratios of VOCs. Instead, model simulations show that secondary OH production causes VOC ratio evolution to follow that expected for OH oxidation, despite the significant input of primary Cl from ClNO2 photolysis in the morning. Even though OH is by far the dominant oxidant in Los Angeles, Cl

  13. Separation of chlorinated diastereomers of decarboxy-betacyanins in myeloperoxidase catalyzed chlorinated Beta vulgaris L. extract.

    Science.gov (United States)

    Wybraniec, Sławomir; Starzak, Karolina; Szneler, Edward; Pietrzkowski, Zbigniew

    2016-11-15

    A comparative chromatographic evaluation of chlorinated decarboxylated betanins and betanidins generated under activity of hypochlorous acid exerted upon these highly antioxidative potent decarboxylated pigments derived from natural sources was performed by LC-DAD-ESI-MS/MS. Comparison of the chromatographic profiles of the chlorinated pigments revealed two different directions of retention changes in relation to the corresponding substrates. Chlorination of all betacyanins that are decarboxylated at carbon C-17 results in an increase of their retention times. In contrast, all other pigments (the non-decarboxylated betacyanins as well as 2-decarboxy- and 15-decarboxy-derivatives) exhibit lower retention after chlorination. During further chromatographic experiments based upon chemical transformation of the related pigments (decarboxylation and deglucosylation), the compounds' structures were confirmed. The elaborated method for determination of chlorinated pigments enabled analysis of a chlorinated red beet root extract that was submitted to the MPO/H 2 O 2 /Cl - system acting under inflammation-like conditions (pH 5). This indicates a promising possibility for measurement of these chlorinated pigments as indicators of specific inflammatory states wherein betacyanins and decarboxylated betacyanins act as hypochlorite scavengers. Copyright © 2016 Elsevier B.V. All rights reserved.

  14. Model studies for evaluating the neurobehavioral effects of complex hydrocarbon solvents. II. Neurobehavioral effects of white spirit in rat and human

    NARCIS (Netherlands)

    Lammers, J.H.C.M.; Emmen, H.H.; Muijser, H.; Hoogendijk, E.M.G.; McKee, R.H.; Owen, D.E.; Kulig, B.M.

    2007-01-01

    To evaluate the neurobehavioral effects of hydrocarbon solvents and to establish a working model for extrapolating animal test data to humans, studies were conducted which involved inhalation exposure of rats and humans to white spirit (WS). The specific objectives of these studies were to evaluate

  15. [Formation mechanism and chemical safety of nonintentional chemical substances present in chlorinated drinking water and wastewater].

    Science.gov (United States)

    Onodera, Sukeo

    2010-09-01

    This paper reviews the formation mechanism and chemical safety of nonintentional chemical substances (NICS) present in chlorine-treated water containing organic contaminants. Undesirable compounds, i.e., NICS, may be formed under certain conditions when chlorine reacts with organic matter. The rate and extent of chlorine consumption with organics are strongly dependent on their chemical structures, particularly whether double bonds or sulfur and nitrogen atoms occur in the molecules. Organothiophosphorus pesticides (P=S type) are easily oxidized to their phosphorus compounds (P=O type) in chlorinated water containing HOCl as little as 0.5 mg/l, resulting in an increase in cholinesterase-inhibitory activity. Chlorination of phenols in water also produces a series of highly chlorinated compounds, including chlorophenols, chloroquinones, chlorinated carboxylic acids, and polychlorinated phenoxyphenols (PCPPs). In some of these chloroquinones, 2,6-dichloroalkylsemiquinones exhibit a strong mutagenic response as do positive controls used in the Ames test. 2-phenoxyphenols in these PCPPs are particularly interesting, as they are present in the chlorine-treated phenol solution and they are also precursors (predioxins) of the highly toxic chlorinated dioxins. Polynuclear aromatic hydrocarbons (PAHs) were found to undergo chemical changes due to hypochlorite reactions to give chloro-substituted PAHs, oxygenated (quinones) and hydroxylated (phenols) compounds, but they exhibit a lower mutagenic response. In addition, field work was performed in river water and drinking water to obtain information on chemical distribution and their safety, and the results are compared with those obtained in the model chlorination experiments.

  16. Chlorine dioxide as phenol and H2S scavenger - formation of halogenated phenols and subsequent environmental risk

    Energy Technology Data Exchange (ETDEWEB)

    Melbye, Alf G.; Faksness, Liv-Guri; Knudsen, Boerre Leif

    2006-03-15

    Formation of halogenated phenols as side products from treatment of produced water with aqueous chlorine dioxide has been investigated. The literature describes formation of halogenated hydrocarbons in effluent treatment using chlorine, hypochlorite and chlorine dioxide. A new chlorine dioxide product, originally intended as a H2S scavenger in the oil and gas industry, has been tested both as a phenol scavenger and H2S-scavenger for produced water applications. The concern about the possible formation of halogenated by-products initiated laboratory testing of chlorine dioxide as phenol and H2S scavenger for produced water applications. The tests also included synthetic matrixes containing phenols, and the tests show that halogenated phenols, mainly brominated species, are found in produced water after treatment with chlorine dioxide. Due to potential environmental risk from halogenated organic contaminants, the use of chlorine dioxide as phenol and H2S scavenger is not recommended. (Author)

  17. Petroleum hydrocarbons

    International Nuclear Information System (INIS)

    Farrington, J.W.; Teal, J.M.; Parker, P.L.

    1976-01-01

    Methods for analysis of petroleum hydrocarbons in marine samples are presented. Types of hydrocarbons present and their origins are discussed. Principles and methods of analysis are outlined. Infrared spectrometry, uv spectrometry, gas chromatography, mass spectroscopy, and carbon 14 measurements are described

  18. Evaluation of thermal-hydraulic performance of hydrocarbon refrigerants during flow boiling in a microchannels array heat sink

    International Nuclear Information System (INIS)

    Chávez, Cristian A.; Leão, Hugo L.S.L.; Ribatski, Gherhardt

    2017-01-01

    Highlights: • Evaluation of refrigerants R600a, R290 and R1270 during flow boiling in a microchannels array. • Comparison of data for hydrocarbons with previous data for R134a. • Parametric analysis of heat transfer coefficient, pressure drop, ONB and exergy behaviors. • Comparison of the experimental data and prediction methods from literature. • In general, refrigerant R290 presents the best performance. - Abstract: The present study concerns an experimental evaluation of the performance of hydrocarbon refrigerants during flow boiling in a microchannels array heat sink. The heat sink is composed of fifty channels with cross sectional areas of 123 × 494 μm"2 and length of 15 mm manufactured in a copper block. Heat transfer coefficient and pressure drop data were obtained for refrigerants R600a, R290 and R1270, mass velocities from 165 to 823 kg/m"2 s, heat fluxes up to 400 kW/m"2, liquid subcooling at the inlet of the test section of 5, 10 and 15 °C and saturation temperature of 25 °C. The data were compared with experimental results obtained in a previous study for R134a and predictions by methods from literature. In general, R290 presented the best performance, providing the highest average heat transfer coefficient and a pressure drop only slightly higher than R1270 that was the fluid presenting the lowest pressure drop. An exergy analysis also revealed the refrigerant R290 as the one presenting the best performance. However, R290 needed the highest excess of superheating to trigger the boiling process (ONB). The methods from literature evaluated in the present study poorly predicted the experimental data for two-phase pressure drop. On the other hand, the method of Kanizawa et al. (2016) was quite accurate in predicting the heat transfer results.

  19. Bioremediation of chlorinated solvents and diesel soils

    International Nuclear Information System (INIS)

    Huismann, S.S.; Peterson, M.A.; Jardine, R.J.

    1995-01-01

    The US Army, in a cooperative effort with the Tennessee Valley Authority (TVA) and its cooperator, ENSR, performed an innovative enhanced bioremediation project at Fort Gillem in Atlanta, Georgia. The objective of the project was to remediate six hundred cubic yards of soil affected by a mixture of chlorinated compounds and petroleum hydrocarbons which posed a threat to uppermost groundwater and private drinking water wells. ENSR completed a demonstration project to measure the effects of bioremediation on both chlorinated compounds (primarily TCE) and petroleum hydrocarbons (number-sign 2 diesel). Contaminated soil was placed on top of a bermed polyethylene liner to construct an ex-situ biovault. Nutrients were added to the soil as it was loaded onto the liner. Contaminated soil was also used to construct a control vault. A methane barrier cover was placed over both piles. The cover was designed to prevent short circuiting of induced airflow in and around the enhanced pile, and to prevent the release of fugitive emissions from either pile

  20. 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.

    Science.gov (United States)

    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 (pturtles 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 ng

  1. Integrated evaluation of the performance of a more than seven year old permeable reactive barrier at a site contaminated with chlorinated aliphatic hydrocarbons (CAHs)

    DEFF Research Database (Denmark)

    Muchitsch, Nanna; Nooten, Thomas Van; Bastiaens, Leen

    2011-01-01

    An important issue of concern for permeable reactive iron barriers is the long-term efficiency of the barriers due to the long operational periods required. Mineral precipitation resulting from the anaerobic corrosion of the iron filings and bacteria present in the barrier may play an important...... performed equally well as virgin granular iron of the same type based on determined degradation rates despite that parts of the cored iron material were covered by mineral precipitates (especially iron sulfides, carbonate green rust and aragonite). The PCR analysis performed on the iron core samples...

  2. Evaluation of landfarm remediation of hydrocarbon-contaminated soil at the Inveresk Railyard, Launceston, Australia

    International Nuclear Information System (INIS)

    Line, M.A.; Garland, C.D.; Crowley, M.

    1996-01-01

    The cost of landfarm bioremediation of hydrocarbon-contaminated soil at a disused railyard site in Tasmania, Australia is reported. The landfarm area was enclosed in an impermeable clay embankment and where necessary the base was also rolled with clay. Microbial inoculation was not deemed to be necessary since suitable degrading biota were found to be present in site samples prior to commencement of the landfarming. Fertilizer amendment comprised primarily ammonium sulphate and superphosphate to give a C:N ratio (TPH:fertilizer) of 28:1 and a C:P ratio of 200:1. The soil was turned regularly and watered as required for the 12-month duration of the operation. Over this period levels of TPH showed a linear decline from a mean of 4,644 mg/kg to near 100 mg/kg or less, with greatest losses being in the chain lengths C10-C28. The cost was determined to be $A13.40c per m 3 , which is at the lower end of the spectrum of reported landfarming costs. The cost of such operations is important since the reported economics will influence others' choice of bioremediation techniques

  3. Chlorine transportation risk assessment

    International Nuclear Information System (INIS)

    Lautkaski, Risto; Mankamo, Tuomas.

    1977-02-01

    An assessment has been made on the toxication risk of the population due to the bulk rail transportation of liquid chlorine in Finland. Fourteen typical rail accidents were selected and their probability was estimated using the accident file of the Finnish State Railways. The probability of a chlorine leak was assessed for each type of accident separately using four leak size categories. The assessed leakage probability was dominated by station accidents, especially by collisions of a chlorine tanker and a locomotive. Toxication hazard areas were estimated for the leak categories. A simple model was constructed to describe the centring of the densely populated areas along the railway line. A comparison was made between the obtained risk and some other risks including those due to nuclear reactor accidents. (author)

  4. Chlorination leaching of cadmium

    International Nuclear Information System (INIS)

    Lach, E.; Pajak, I.; Bojanowska, A.

    1978-01-01

    The results of the investigations on chlorination leaching of cadmium from dust coming from dry dust collector of sinter belt, that is leaching with water saturated with gaseous chlorine and leaching with solutions of ammonium chloride and sodium chloride were given. The optimum conditions for these processes were established. It was found, that the method of leaching in the presence of gaseous chlorine is more effective, as it allows to report into the solution over 90% cadmium contained in dust. Owing to technical difficulties, environmental protection and safety conditions more advantageous seems to be the use as leaching agent of the ammonium chloride solutions. When applying 20% NH 4 Cl and temperature of 60 0 C, the time of 2 hours and the ratio of solid to liquid of 1:5, 70% cadmium contained in the dust can be reported into the solution. (auth.)

  5. Surface geochemical data evaluation and integration with geophysical observations for hydrocarbon prospecting, Tapti graben, Deccan Syneclise, India

    OpenAIRE

    Satish Kumar, T.; Dayal, A.M.; Sudarshan, V.

    2014-01-01

    The Deccan Syneclise is considered to have significant hydrocarbon potential. However, significant hydrocarbon discoveries, particularly for Mesozoic sequences, have not been established through conventional exploration due to the thick basalt cover over Mesozoic sedimentary rocks. In this study, near-surface geochemical data are used to understand the petroleum system and also investigate type of source for hydrocarbons generation of the study area. Soil samples were collected from favorable...

  6. Evaluation of bacterial strategies to promote the bioavailability of polycyclic aromatic hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Johnsen, A.R.; Karlson, U. [Dept. of Environmental Chemistry and Microbiology, National Environmental Research Inst., Roskilde (Denmark)

    2004-07-01

    Polycyclic aromatic hydrocarbon (PAHs)-degrading bacteria may enhance the bioavailability of PAHs by excreting biosurfactants, by production of extracellular polymeric substances, or by forming biofilms. We tested these hypotheses in pure cultures of PAHs-degrading bacterial strains. Most of the strains did not substantially reduce the surface tension when grown on PAHs in liquid shaken cultures. Thus, pseudo-solubilization of PAHs in biosurfactant micelles seems not to be a general strategy for these isolates to enhance PAHs-bioavailability. Three semi-colloid Sphingomonas polysaccharides all increased the solubility of PAHs (Gellan 1.3- to 5.4-fold, Welan 1.8- to 6.0-fold and Rhamsan 2.4- to 9.0-fold). The increases were most pronounced for the more hydrophobic PAHs. The polysaccharide-sorbed PAHs were bioavailable. Mineralization rates of 9-[{sup 14}C]-phenanthrene and 3-[{sup 14}C]-fluoranthene by Sphingobium EPA505, were similar with and without sphingans, indicating that mass-transfer rates from PAHs crystals to the bulk liquid were unaffected by the polysaccharides. Biofilm formation on PAHs crystals may favor the diffusive mass transfer of PAHs from crystals to the bacterial cells. A majority of the PAHs-degraders tested formed biofilms in microtiter wells coated with PAHs crystals. For strains capable of growing on different PAHs; the more soluble the PAHs, the lower the percentage of cells attached. Biofilm formation on PAHs-sources was the predominant mechanism among the tested bacteria to overcome mass transfer limitations when growing on poorly soluble PAHs. (orig.)

  7. Proton conducting hydrocarbon membranes: Performance evaluation for room temperature direct methanol fuel cells

    International Nuclear Information System (INIS)

    Krivobokov, Ivan M.; Gribov, Evgeniy N.; Okunev, Alexey G.

    2011-01-01

    The methanol permeability, proton conductivity, water uptake and power densities of direct methanol fuel cells (DMFCs) at room temperature are reported for sulfonated hydrocarbon (sHC) and perfluorinated (PFSA) membranes from Fumatech, and compared to Nafion membranes. The sHC membranes exhibit lower proton conductivity (25-40 mS cm -1 vs. ∼95-40 mS cm -1 for Nafion) as well as lower methanol permeability (1.8-3.9 x 10 -7 cm 2 s -1 vs. 2.4-3.4 x 10 -6 cm 2 s -1 for Nafion). Water uptake was similar for all membranes (18-25 wt%), except for the PFSA membrane (14 wt%). Methanol uptake varied from 67 wt% for Nafion to 17 wt% for PFSA. The power density of Nafion in DMFCs at room temperature decreases with membrane thickness from 26 mW cm -2 for Nafion 117 to 12.5 mW cm -2 for Nafion 112. The maximum power density of the Fumatech membranes ranges from 4 to 13 mW cm -1 . Conventional transport parameters such as membrane selectivity fail to predict membrane performance in DMFCs. Reliable and easily interpretable results are obtained when the power density is plotted as a function of the transport factor (TF), which is the product of proton concentration in the swollen membrane and the methanol flux. At low TF values, cell performance is limited by low proton conductivity, whereas at high TF values it decreases due to methanol crossover. The highest maximum power density corresponds to intermediate values of TF.

  8. Inactivation of Aspergillus flavus in drinking water after treatment with UV irradiation followed by chlorination

    International Nuclear Information System (INIS)

    Al-Gabr, Hamid Mohammad; Zheng, Tianling; Yu, Xin

    2013-01-01

    The disinfection process for inactivating microorganisms at drinking water treatment plants is aimed for safety of drinking water for humans from a microorganism, such as bacteria, viruses, algae, fungi by using chlorination, ozonation, UV irradiation, etc. In the present study, a combination of two disinfectants, UV irradiation followed by chlorination, was evaluated for inactivating Aspergillus flavus under low contact time and low dosage of UV irradiation. The results indicated an inverse correlation between the inactivation of A. flavus by using UV irradiation only or chlorination alone. By using UV radiation, the 2 log 10 control of A. flavus was achieved after 30 s of irradiation, while chlorination was observed to be more effective than UV, where the 2 log was achieved at chlorine concentration of 0.5, 1, 2 and 3 mg/l, in contact time of 60, 5, 1 and 1 min, respectively. However, combined use (UV irradiation followed by chlorination) was more effective than using either UV or chlorination alone; 5 s UV irradiation followed by chlorination produced 4 log 10 reduction of A. flavus at chlorine concentrations of 2 and 3 mg/l under a contact time of 15 min. The results indicated that efficiency of UV irradiation improves when followed by chlorination at low concentrations. - Highlights: • As a disinfectant, chlorine is more effective than UV in inactivating Aspergillus flavus. • As a combined method, UV irradiation followed by chlorination shows high efficiency. • UV irradiation can improve effectiveness of chlorination in reducing Aspergillus flavus

  9. Diagnostic Tools for Performance Evaluation of Innovative In-Situ Remediation Technologies at Chlorinated Solvent-Contaminated Sites

    Science.gov (United States)

    2011-07-01

    isotope analysis. II International Seminar on In-Situ Remediation of Contaminated Sites, Sao Paulo , Brazil , November 3-5, 2003. Hunkeler, D., R...the contami- nated area. Phase 2 was a longer-term permanganate delivery designed to flood certain areas with sufficient permanganate to evaluate...KMnO4 injections into MW-65 and MW-71 (see Exhibit 4) in April, May, and June 2002, with the purpose of flooding these areas and achieving KMnO4 diffusion

  10. Removal of sulfamethoxazole, ibuprofen and nitrobenzene by UV and UV/chlorine processes: A comparative evaluation of 275 nm LED-UV and 254 nm LP-UV.

    Science.gov (United States)

    Kwon, Minhwan; Yoon, Yeojoon; Kim, Seonbaek; Jung, Youmi; Hwang, Tae-Mun; Kang, Joon-Wun

    2018-05-15

    The aim of this study is to evaluate the micropollutant removal capacity of a 275 nm light-emitting diode (LED)-UV/chlorine system. The sulfamethoxazole, ibuprofen, and nitrobenzene removal efficiencies of this system were compared with those of a conventional 254 nm low-pressure (LP)-UV system as a function of the UV dose. In a direct photolysis system, the photon reactivity of sulfamethoxazole is higher than that of nitrobenzene and ibuprofen at both wavelengths. The molar absorption coefficients and quantum yields of each micropollutant were as follows: sulfamethoxazole (ε SMX, 275 nm protonated  = 17,527 M -1  cm -1 , Φ SMX, 275 nm protonated  = 0.239, ε SMX, 275 nm deprotonated  = 8430 M -1  cm -1 , and Φ SMX, 275 nm deprotonated  = 0.026), nitrobenzene (ε NB, 275 nm  = 7176 M -1  cm -1 and Φ NB, 275 nm  = 0.057), and ibuprofen (ε NB, 275 nm  = 200 M -1  cm -1 and Φ IBF, 275 nm  = 0.067). The photon reactivity of chlorine species, i.e., HOCl and OCl-, were determined at 275 nm (ε HOCl, 275 nm  = 28 M -1  cm -1 , Φ HOCl, 275 nm  = 1.97, ε OCl-, 275 nm  = 245 M -1  cm -1 , and Φ OCl-, 275 nm  = 0.8), which indicate that the decomposition rate of OCl - is higher and that of HOCl is lower by 275 nm photolysis than that by 254 nm photolysis (ε HOCl, 254 nm  = 60 M -1  cm -1 , Φ HOCl, 254 nm  = 1.46, ε OCl-, 254 nm  = 58 M -1  cm -1 , and Φ OCl-, 254 nm  = 1.11). In the UV/chlorine system, the removal rates of ibuprofen and nitrobenzene were increased by the formation of OH and reactive chlorine species. The 275-nm LED-UV/chlorine system has higher radical yields at pH 7 and 8 than the 254 nm LP-UV/chlorine system. Copyright © 2018 Elsevier B.V. All rights reserved.

  11. Where does Chlorine-36 go?

    International Nuclear Information System (INIS)

    Anon.

    2000-01-01

    Chlorine-36 and Iodine-129 are the unique long-life radionuclides in the halogen family and halogens are known to be very mobile in the environment. Chlorine-36 is present in slight quantities in radioactive wastes containing carbon or issued from spent fuel reprocessing. The migration of Chlorine-36 in the environment has been very little studied, so a collaboration between the French institute of protection and nuclear safety (IPSN) and the Ukrainian institute for agricultural radioecology (UIAR) has been launched. IPSN will study the migration of Chlorine-36 in soils and UIAR will be in charge of studying the transfer of Chlorine-36 from soil to plants. (A.C.)

  12. Model-based evaluation of the use of polycyclic aromatic hydrocarbons molecular diagnostic ratios as a source identification tool

    International Nuclear Information System (INIS)

    Katsoyiannis, Athanasios; Breivik, Knut

    2014-01-01

    Polycyclic Aromatic Hydrocarbons (PAHs) molecular diagnostic ratios (MDRs) are unitless concentration ratios of pair-PAHs with the same molecular weight (MW); MDRs have long been used as a tool for PAHs source identification purposes. In the present paper, the efficiency of the MDR methodology is evaluated through the use of a multimedia fate model, the calculation of characteristic travel distances (CTD) and the estimation of air concentrations for individual PAHs as a function of distance from an initial point source. The results show that PAHs with the same MW are sometimes characterized by substantially different CTDs and therefore their air concentrations and hence MDRs are predicted to change as the distance from the original source increases. From the assessed pair-PAHs, the biggest CTD difference is seen for Fluoranthene (107 km) vs. Pyrene (26 km). This study provides a strong indication that MDRs are of limited use as a source identification tool. -- Highlights: • Model-based evaluation of the PAHs molecular diagnostic ratios efficiency. • Individual PAHs are characterized by different characteristic travel distances. • MDRs are proven to be a limited tool for source identification. • Use of MDRs for other environmental media is likely unfeasible. -- PAHs molecular diagnostic ratios which change greatly as a function of distance from the emitting source are improper for source identification purposes

  13. Copaiba oleoresin: evaluation of the presence of polycyclic aromatic hydrocarbons (PAHs

    Directory of Open Access Journals (Sweden)

    Wilson Gomes da Silva

    2010-09-01

    Full Text Available The copaiba oleoresin extracted by perforating the tree-trunk found in the Amazonian forest has been used by the native indigenous communities to treat several diseases and also as fuel for lighting and for the motorboats plying the region's rivers. Currently, the oleoresin is mostly employed as a traditional remedy, mainly for the treatment of tonsillitis and as an anti-inflammatory and healing agent in oil and capsule forms, and is also used in several industry sectors. Due to its use in oral form, especially as a traditional remedy, an analysis of the presence of polycyclic aromatic hydrocarbons (PAHs as contaminants in the oleoresin was performed. PAHs are substances formed by two or more benzoic rings and found in the atmosphere as a residue from incomplete combustion of petroleum derivatives and industrial activities. These substances are found everywhere on land and water, and as a consequence can also be found in vegetables and foodstuffs in general. The use of products contaminated with these substances can compromise human and animal life. This study was performed on oleoresin from different areas or regions in the Amazon, using the HPLC methodology with fluorescence detection. The samples analyzed revealed different concentrations of these compounds.O óleo-resina de copaíba que é extraído mediante a perfuração do tronco da árvore que se encontra em forma nativa na floresta amazônica já era empregado pelas comunidades indígenas para a cura de várias doenças e, também, como combustível em iluminação e para o funcionamento de motores de barcos que trafegavam pelos rios da região. Hoje, é largamente empregado na medicina popular, principalmente para o tratamento de amigdalite e como antiinflamatório e cicatrizante na forma de óleo e em cápsulas, sendo utilizado, também, em vários setores da indústria. Devido ao seu uso na forma oral, principalmente na medicina popular, realizou-se um trabalho para avaliar a presen

  14. Evaluation of the performance and response of the bacharach TLV sniffer and H-Nu photoionization gas analyzer to common hydrocarbon solvents.

    Science.gov (United States)

    Chelton, C F; Zakraysek, N; Lautner, G M; Confer, R G

    1983-10-01

    Two direct reading instruments, the H-Nu PI 101 photoionization analyzer and the J.W. Bacharach TLV Sniffer, were evaluated under laboratory conditions to determine their performance characteristics when challenged by vapors of common hydrocarbon solvent mixtures. Each instrument was evaluated against the manufacturer's recommended test solvent for rise time, fall time, noise, span drift, zero drift, position sensitivity, battery life, and recharge time. The precision, accuracy, and operating linear range were also determined for the test solvents and some petroleum solvent mixtures which are common refinery products. For these latter mixtures, correction factors are presented which allow for an improved estimate of ambient concentrations when monitoring with each of these instruments. All tests except operating humidity range were performed by challenging each instrument with a known concentration of hydrocarbon generated by evaporating calculated liquid volumes into a static chamber. Humidity tests were performed using a dynamic dilution apparatus generating a fixed concentration of hydrocarbon while relative humidity was varied. Concentrations in both systems were verified by gas injection into gas chromatograph. Each instrument performed well when challenged by manufacturers' recommended test solvents. Humidity was shown to influence each instrument's readings. Also, the instruments were shown to have application as monitors of airborne concentrations of common hydrocarbon solvent mixtures.

  15. Chlorine inactivation of Tubifex tubifex in drinking water and the synergistic effect of sequential inactivation with UV irradiation and chlorine.

    Science.gov (United States)

    Nie, Xiao-Bao; Li, Zhi-Hong; Long, Yuan-Nan; He, Pan-Pan; Xu, Chao

    2017-06-01

    The inactivation of Tubifex tubifex is important to prevent contamination of drinking water. Chlorine is a widely-used disinfectant and the key factor in the inactivation of T. tubifex. This study investigated the inactivation kinetics of chlorine on T. tubifex and the synergistic effect of the sequential use of chlorine and UV irradiation. The experimental results indicated that the Ct (concentration × time reaction ) concept could be used to evaluate the inactivation kinetics of T. tubifex with chlorine, thus allowing for the use of a simpler Ct approach for the assessment of T. tubifex chlorine inactivation requirements. The inactivation kinetics of T. tubifex by chlorine was found to be well-fitted to a delayed pseudo first-order Chick-Watson expression. Sequential experiments revealed that UV irradiation and chlorine worked synergistically to effectively inactivate T. tubifex as a result of the decreased activation energy, E a , induced by primary UV irradiation. Furthermore, the inactivation effectiveness of T. tubifex by chlorine was found to be affected by several drinking water quality parameters including pH, turbidity, and chemical oxygen demand with potassium permanganate (COD Mn ) concentration. High pH exhibited pronounced inactivation effectiveness and the decrease in turbidity and COD Mn concentrations contributed to the inactivation of T. tubifex. Copyright © 2017 Elsevier Ltd. All rights reserved.

  16. Chlorine signal attenuation in concrete.

    Science.gov (United States)

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

    2015-11-01

    The intensity of prompt gamma-ray was measured at various depths from chlorine-contaminated silica fume (SF) concrete slab concrete specimens using portable neutron generator-based prompt gamma-ray setup. The intensity of 6.11MeV chloride gamma-rays was measured from the chloride contaminated slab at distance of 15.25, 20.25, 25.25, 30.25 and 35.25cm from neutron target in a SF cement concrete slab specimens. Due to attenuation of thermal neutron flux and emitted gamma-ray intensity in SF cement concrete at various depths, the measured intensity of chlorine gamma-rays decreases non-linearly with increasing depth in concrete. A good agreement was noted between the experimental results and the results of Monte Carlo simulation. This study has provided useful experimental data for evaluating the chloride contamination in the SF concrete utilizing gamma-ray attenuation method. Copyright © 2015 Elsevier Ltd. All rights reserved.

  17. Germination of Lepidium sativum as a method to evaluate polycyclic aromatic hydrocarbons (PAHs) removal from contaminated soil

    CSIR Research Space (South Africa)

    Maila, MP

    2002-01-01

    Full Text Available The sensitivity of Lepidium sativum germination to polycyclic aromatic hydrocarbons (PAHs) was investigated in soil(s) artificially and historically contaminated with mixtures of PAR The level of germination of L. sativum decreased with increasing...

  18. Comparative evaluation of ICP sample introduction systems to be used in the metabolite profiling of chlorine-containing pharmaceuticals via HPLC-ICP-MS.

    Science.gov (United States)

    Klencsár, Balázs; Sánchez, Carlos; Balcaen, Lieve; Todolí, José; Lynen, Frederic; Vanhaecke, Frank

    2018-05-10

    A systematic evaluation of four different ICP sample introduction systems to be used in the context of metabolite profiling of chlorine-containing pharmaceuticals via HPLC-ICP-MS was carried out using diclofenac and its major metabolite, 4'-hydroxy-diclofenac, as model compounds. The strict requirements for GMP validation of chromatographic methods in the pharmaceutical industry were adhered to in this context. The final aim of this investigation is an extension of the applicability and validatability of HPLC-ICP-MS in the field of pharmaceutical R&D. Five different gradient programmes were tested while the baseline peak width (w b ), peak capacity (P), USP tailing factor (A s ) and USP signal-to-noise ratio (USP S/N) were determined as major indicators of the chromatographic performance and the values obtained were compared to the corresponding FDA recommendations (if applicable). Four different ICP-MS sample introductions systems were investigated involving two units typically working at higher flow rates (∼1.0 mL min -1 ) and another two systems working at lower flow rates (∼0.1 mL min -1 ). Optimal conditions with potential for applicability under GMP conditions were found at a mobile phase flow rate of 1.0 mL min -1 by using a pneumatic micro-flow LC nebulizer mounted onto a Peltier-cooled cyclonic spray chamber cooled to -1 °C for sample introduction. Under these conditions, HPLC-ICP-MS provided a chromatographic performance similar to that of HPLC with UV detection. The peak shape (USP tailing factor = 1.1-1.4) was significantly improved compared to that obtained with the Peltier-cooled Scott-type spray chamber. Two alternative sample introduction systems - a POINT ® and a High-Temperature Torch-Integrated Sample Introduction System (hTISIS) - were also tested at a flow rate of 0.1 mL min -1 using a chromatographic column with 1.0 mm ID. Although these systems allowed the peak shape to be improved compared to that obtained with

  19. Chlorination of zirconyte concentrate

    International Nuclear Information System (INIS)

    Costa, N.G.

    1988-01-01

    Chlorination experiments with zirconyte concentrate were carried out in order to study the effects of temperature, percentage of reducing agent and porosity on the gasification of ZrO 2 for 10 and 20 minutes of reaction. Factorial analysis was applied and the results indicated that temperature and percentage of reducing agent were the two only variables effecting the ZrO 2 gasification. (author) [pt

  20. Evaluation on occluded hydrocarbon in deep–ultra deep ancient source rocks and its cracked gas resources

    Directory of Open Access Journals (Sweden)

    Jian Li

    2015-12-01

    Full Text Available Oil-cracked gas, as the main type of high-over mature marine natural gas in China, is mainly derived from occluded hydrocarbon. So it is significant to carry out quantitative study on occluded hydrocarbon. In this paper, the occluded hydrocarbon volume of the main basins in China was calculated depending on their types, abundances and evolution stages by means of the forward method (experimental simulation and the inversion method (geologic profile dissection. And then, occluded hydrocarbon evolution models were established for five types of source rocks (sapropelic, sapropelic prone hybrid, humic prone hybrid, humic and coal. It is shown that the hydrocarbon expulsion efficiency of sapropelic and sapropelic prone hybrid excellent source rocks is lower than 30% at the low-maturity stage, 30%–60% at the principal oil generation stage, and 50%–80% at the high-maturity stage, which are all about 10% higher than that of humic prone hybrid and humic source rocks at the corresponding stages. The resource distribution and cracked gas expulsion of occluded hydrocarbon since the high-maturity stage of marine source rocks in the Sichuan Basin were preliminarily calculated on the basis of the evolution models. The cracked gas expulsion is 230.4 × 1012 m3 at the high evolution stage of occluded hydrocarbon of the Lower Cambrian Qiongzhusi Fm in this basin, and 12.3 × 1012 m3 from the source rocks of Sinian Doushantuo Fm, indicating good potential for natural gas resources. It is indicated that the favorable areas of occluded hydrocarbon cracked gas in the Qiongzhusi Fm source rocks in the Sichuan Basin include Gaoshiti–Moxi, Ziyang and Weiyuan, covering a favorable area of 4.3 × 104 km2.

  1. Purifying hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Dunstan, A E

    1918-06-03

    Ligroin, kerosene, and other distillates from petroleum and shale oil, are purified by treatment with a solution of a hypochlorite containing an excess of alkali. The hydrocarbon may be poured into brine, the mixture stirred, and an electric current passed through. Heat may be applied.

  2. Surface geochemical data evaluation and integration with geophysical observations for hydrocarbon prospecting, Tapti graben, Deccan Syneclise, India

    Directory of Open Access Journals (Sweden)

    T. Satish Kumar

    2014-05-01

    Full Text Available The Deccan Syneclise is considered to have significant hydrocarbon potential. However, significant hydrocarbon discoveries, particularly for Mesozoic sequences, have not been established through conventional exploration due to the thick basalt cover over Mesozoic sedimentary rocks. In this study, near-surface geochemical data are used to understand the petroleum system and also investigate type of source for hydrocarbons generation of the study area. Soil samples were collected from favorable areas identified by integrated geophysical studies. The compositional and isotopic signatures of adsorbed gaseous hydrocarbons (methane through butane were used as surface indicators of petroleum micro-seepages. An analysis of 75 near-surface soil-gas samples was carried out for light hydrocarbons (C1–C4 and their carbon isotopes from the western part of Tapti graben, Deccan Syneclise, India. The geochemical results reveal sites or clusters of sites containing anomalously high concentrations of light hydrocarbon gases. High concentrations of adsorbed thermogenic methane (C1 = 518 ppb and ethane plus higher hydrocarbons (ΣC2+ = 977 ppb were observed. Statistical analysis shows that samples from 13% of the samples contain anomalously high concentrations of light hydrocarbons in the soil-gas constituents. This seepage suggests largest magnitude of soil gas anomalies might be generated/source from Mesozoic sedimentary rocks, beneath Deccan Traps. The carbon isotopic composition of methane, ethane and propane ranges are from −22.5‰ to −30.2‰ PDB, −18.0‰ to 27.1‰ PDB and 16.9‰–32.1‰ PDB respectively, which are in thermogenic source. Surface soil sample represents the intersection of a migration conduit from the deep subsurface to the surface connected to sub-trappean Mesozoic sedimentary rocks. Prominent hydrocarbon concentrations were associated with dykes, lineaments and presented on thinner basaltic cover in the study area

  3. A re-circulated toxicity exposure chamber to evaluate hydrocarbon dispersions

    International Nuclear Information System (INIS)

    Fuller, C.B.; Bonner, J.S.; Bujnoch, J.D.; Ussery, S.F.; Arrambide, G.; Sterling, M.C.

    2002-01-01

    Traditional toxicology methods are not suitable for evaluating chemically dispersed oil which exists mostly as a colloidal suspension and as dissolved fractions. A new toxicity exposure chamber was designed with separate chambers for scaled mixing and organism exposure. The design of the chamber incorporates continuous recirculation between the mixing and exposure chamber and an upward flow in the exposure chamber. The toxicity exposure system incorporates scalable and quantitative mixing inputs with real time particle size analysis and traditional petrochemistry methods to characterize the exposure regime. Changes in dispersion were successfully translated to the organism exposure regime. The study determined the petroleum toxicity with a juvenile marine test species. Low control mortality demonstrated the usefulness of the method for testing toxicity of colloidal oil suspensions. 20 refs., 1 tab., 4 figs

  4. Photophysical properties and localization of chlorins substituted with methoxy groups, hydroxyl groups and alkyl chains in liposome-like cellular membrane

    Energy Technology Data Exchange (ETDEWEB)

    Al-Omari, S [Department of Physics, Hashemite University, Zarqa 13115 (Jordan)

    2007-06-01

    Some of the photophysical properties (stationary absorbance and fluorescence, fluorescence decay times and singlet oxygen quantum yields) of chlorins substituted with methoxy groups, hydroxyl groups and hydrocarbonic chains were studied in ethanol and dipalmitoyl-phosphatidylcholine (DPPC) liposomes using steady-state and time-resolved fluorescence spectroscopies. The photophysical behaviors of the chlorins in liposomes like cellular membrane were compared with those obtained from chlorin-liposome systems delivered to Jurkat cells in order to select potent photosensitizers for the photodynamic treatment of cancer. The localization of the studied chlorins inside liposomes was found to depend strongly on the substituents of chlorins. Absorption spectra of chlorins embedded in DPPC-liposomes have been recorded in the temperature range of 20-70 deg. C. It is demonstrated that the location of the chlorin molecules depends on the phase state of the phospholipids. These observations are confirmed by the fluorescence lifetimes, singlet oxygen lifetimes and singlet oxygen quantum yields results.

  5. Evaluation of dissipation gradients of polycyclic aromatic hydrocarbons in rice rhizosphere utilizing a sequential extraction procedure

    International Nuclear Information System (INIS)

    Ma Bin; Wang Jiaojiao; Xu Minmin; He Yan; Wang Haizhen; Wu Laosheng; Xu Jianming

    2012-01-01

    The aim of this study was to evaluate the spatial dissipation gradient of PAHs, including phenanthrene, pyrene, and benzo[a]pyrene, with various bioavailability represented with sequential extraction. Dissipation rates of PAHs in the rhizosphere were greater than those in the bulk soil. The n-butanol extracted fraction showed a general trend of dissipation during phytoremediation. Moreover, the formation of bound PAH residues was inhibited in the rhizosphere. While concerning the PAH toxicity, the reduction rates of PAH toxicity were significantly greater than total soil PAH concentrations. Microbial biomass was the highest at four mm away from the root surface. However, the PAH dissipation rates were the highest at one mm and two mm away from the root surface in high and low PAH treatments, respectively. These results suggest that rhizoremediation with rice is a useful approach to reduce the toxicity of PAHs in soil. - Highlights: ► Dissipation gradients were different in soils spiked with different PAHs concentrations. ► Butanol extracted fraction indicated the remediation in rhizosphere. ► Toxicity of PAHs was more efficiently reduced than total concentration. ► Promotion of PAHs degraders was not synchronized with microbial biomass. - Stimulation of PAH degradation in rice rhizosphere was not simultaneous with microbial biomass.

  6. Thermal degradation of sucralose: a combination of analytical methods to determine stability and chlorinated byproducts

    Science.gov (United States)

    de Oliveira, Diogo N.; de Menezes, Maico; Catharino, Rodrigo R.

    2015-04-01

    In the late years, much attention has been brought to the scientific community regarding the safety of sucralose and its industrial applications. Although it is the most used artificial sweetener in foods and pharmaceuticals, many questions still arise on its potential to form chlorinated byproducts in high temperatures, as demonstrated by several recent studies. In the present contribution, we use a combination of differential scanning calorimetry and thermogravimetric analysis coupled with infrared spectroscopy (DSC/TGA/IR), Hot-stage microscopy (HSM) and high-resolution mass spectrometry (HRMS) on samples submitted to water bath at mild temperatures to evaluate a broad spectrum of hazardous compounds formed in the degradation of this product. TGA/IR has revealed that there is effective decomposition in form of CO2 along with the formation of hydrogen chloride and other minor compounds. HSM results have provided accurate information, where the melting of the crystals was observed, followed by decomposition. Chlorinated derivatives, including polychlorinated aromatic hydrocarbons (PCAHs) were also confirmed by HRMS. These findings not only corroborate the suspected instability of sucralose to high temperatures, but also indicate that even exposed to mild conditions the formation of hazardous polychlorinated compounds is observed.

  7. Environmentally acceptable incineration of chlorinated chemical waste : Review of theory and practice

    NARCIS (Netherlands)

    De Zeeuw, M.A.; Lemkowitz, S.M.

    1987-01-01

    Chlorinated hydrocarbons in the form of chemical waste, represent a threat to the environment and public health of the world. Their proper handling, removal and destruction is critical to long term safety. Increasingly strict government legislation is leading to an increase in the quantity of

  8. Epidemiological evidence of carcinogenicity of chlorinated organics in drinking water.

    OpenAIRE

    Cantor, K P

    1982-01-01

    Concern has recently been voiced over possible chronic toxicity associated with chlorination of public drinking water supplies in the United States. This paper reviews the available evidence and the studies underway to further evaluate hypothesized associations between cancer risk and byproducts of chlorination. Preliminary data from measures of halogenated volatiles and personal exposure histories from respondents in a large epidemiologic study of bladder cancer are presented. These data sup...

  9. Studies on degradation of chlorinated aromatic hydrocarbon by ...

    African Journals Online (AJOL)

    SERVER

    2007-06-04

    Jun 4, 2007 ... chlorobenzene to study the kinetics of degradation of chlorobenzene. The rate of decomposition of ... hydraulic fluids, biocides, herbicides, plastics, degree- ..... degradation by bacteria isolated from contaminated groundwater.

  10. Site remediation using photocatalytic VOC destruction of chlorinated hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    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.

  11. Studies on degradation of chlorinated aromatic hydrocarbon by ...

    African Journals Online (AJOL)

    In this work Pseudomonas aeruginosa (NCIM-2074) has been identified as potential organism to decompose chlorobenzene by its crude extract through immobilization technique. P. aeruginosa was grown on chlorobenzene as sole source of carbon and energy. Chlorobenzene was used as an inducer to develop specific ...

  12. Biological Chlorine Cycling in Arctic Peat Soils

    Science.gov (United States)

    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

  13. The occupational exposure of dermatology nurses to polycyclic aromatic hydrocarbons - evaluating the effectiveness of better skin protection.

    NARCIS (Netherlands)

    Scheepers, P.T.J.; Houtum, J.L.M. van; Anzion, R.B.M.; Champmartin, C.; Hertsenberg, S.; Bos, R.P.; Valk, P. van der

    2009-01-01

    OBJECTIVES: We studied the uptake of polycyclic aromatic hydrocarbons (PAH) in nurses who apply ointments containing coal tar to patients and investigated the effectiveness of skin protection methods. METHODS: We determined gas-phase PAH on XAD-2 and particle-associated PAH on filters. We also used

  14. Determination of volatile organic hydrocarbons in water samples by solid-phase dynamic extraction.

    Science.gov (United States)

    Jochmann, Maik A; Yuan, Xue; Schmidt, Torsten C

    2007-03-01

    In the present study a headspace solid-phase dynamic extraction method coupled to gas chromatography-mass spectrometry (HS-SPDE-GC/MS) for the trace determination of volatile halogenated hydrocarbons and benzene from groundwater samples was developed and evaluated. As target compounds, benzene as well as 11 chlorinated and brominated hydrocarbons (vinyl chloride, dichloromethane, cis-1,2-dichloroethylene, trans-1,2-dichloroethylene, carbon tetrachloride, chloroform, trichloroethylene, tetrachloroethylene, bromoform) of environmental and toxicological concern were included in this study. The analytes were extracted using a SPDE needle device, coated with a poly(dimethylsiloxane) with 10% embedded activated carbon phase (50-microm film thickness and 56-mm film length) and were analyzed by GC/MS in full-scan mode. Parameters that affect the extraction yield such as extraction and desorption temperature, salting-out, extraction and desorption flow rate, extraction volume and desorption volume, the number of extraction cycles, and the pre-desorption time have been evaluated and optimized. The linearity of the HS-SPDE-GC/MS method was established over several orders of magnitude. Method detection limits (MDLs) for the compounds investigated ranged between 12 ng/L for cis-dichloroethylene and trans-dichloroethylene and 870 ng/L for vinyl chloride. The method was thoroughly validated, and the precision at two concentration levels (0.1 mg/L and a concentration 5 times above the MDL) was between 3.1 and 16% for the analytes investigated. SPDE provides high sensitivity, short sample preparation and extraction times and a high sample throughput because of full automation. Finally, the applicability to real environmental samples is shown exemplarily for various groundwater samples from a former waste-oil recycling facility. Groundwater from the site showed a complex contamination with chlorinated volatile organic compounds and aromatic hydrocarbons.

  15. Determination of volatile organic hydrocarbons in water samples by solid-phase dynamic extraction

    Energy Technology Data Exchange (ETDEWEB)

    Jochmann, Maik A.; Schmidt, Torsten C. [Eberhard-Karls-Universitaet Tuebingen, Center for Applied Geoscience (ZAG), Tuebingen (Germany); Chair of Instrumental Analysis, University Duisburg-Essen, Duisburg (Germany); Yuan, Xue [Eberhard-Karls-Universitaet Tuebingen, Center for Applied Geoscience (ZAG), Tuebingen (Germany)

    2007-03-15

    In the present study a headspace solid-phase dynamic extraction method coupled to gas chromatography-mass spectrometry (HS-SPDE-GC/MS) for the trace determination of volatile halogenated hydrocarbons and benzene from groundwater samples was developed and evaluated. As target compounds, benzene as well as 11 chlorinated and brominated hydrocarbons (vinyl chloride, dichloromethane, cis-1,2-dichloroethylene, trans-1,2-dichloroethylene, carbon tetrachloride, chloroform, trichloroethylene, tetrachloroethylene, bromoform) of environmental and toxicological concern were included in this study. The analytes were extracted using a SPDE needle device, coated with a poly(dimethylsiloxane) with 10% embedded activated carbon phase (50-{mu}m film thickness and 56-mm film length) and were analyzed by GC/MS in full-scan mode. Parameters that affect the extraction yield such as extraction and desorption temperature, salting-out, extraction and desorption flow rate, extraction volume and desorption volume, the number of extraction cycles, and the pre-desorption time have been evaluated and optimized. The linearity of the HS-SPDE-GC/MS method was established over several orders of magnitude. Method detection limits (MDLs) for the compounds investigated ranged between 12 ng/L for cis-dichloroethylene and trans-dichloroethylene and 870 ng/L for vinyl chloride. The method was thoroughly validated, and the precision at two concentration levels (0.1 mg/L and a concentration 5 times above the MDL) was between 3.1 and 16% for the analytes investigated. SPDE provides high sensitivity, short sample preparation and extraction times and a high sample throughput because of full automation. Finally, the applicability to real environmental samples is shown exemplarily for various groundwater samples from a former waste-oil recycling facility. Groundwater from the site showed a complex contamination with chlorinated volatile organic compounds and aromatic hydrocarbons. (orig.)

  16. Cracking hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Forwood, G F; Lane, M; Taplay, J G

    1921-10-07

    In cracking and hydrogenating hydrocarbon oils by passing their vapors together with steam over heated carbon derived from shale, wood, peat or other vegetable or animal matter, the gases from the condenser are freed from sulfuretted hydrogen, and preferably also from carbon dioxide, and passed together with oil vapors and steam through the retort. Carbon dioxide may be removed by passage through slaked lime, and sulfuretted hydrogen by means of hydrated oxide of iron. Vapors from high-boiling oils and those from low-boiling oils are passed alternately through the retort, so that carbon deposited from the high-boiling oils is used up during treatment of low-boiling oils.

  17. Distilling hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Bataafsche, N V; de Brey, J H.C.

    1918-10-30

    Hydrocarbons containing a very volatile constituent and less volatile constituents, such as casing-head gases, still gases from the distillation of crude petroleum and bituminous shale are separated into their constituents by rectification under pressure; a pressure of 20 atmospheres and limiting temperatures of 150/sup 0/C and 40/sup 0/C are mentioned as suitable. The mixture may be subjected to a preliminary treatment consisting in heating to a temperature below the maximum rectification temperature at a pressure greater than that proposed to be used in the rectification.

  18. Studies with solid chlorine chemical for chlorination of sea water systems

    International Nuclear Information System (INIS)

    Sankar, N.; Kumaraswamy, P.; Santhanam, V.S.; Jeena, P.; Hari Krishna, K.; Rajendran, D.

    2015-01-01

    Chlorination is one of the conventional methods to control biofouling of condenser cooling water systems using either river water, reservoir water or sea water. However, there are many safety concerns associated with handling, storage and application of gaseous chlorine. Studies were carried out with suitable alternative chlorine chemical compounds which do not involve majority of these concerns but meet the functional requirement of gas chlorine. Trichloroisocyanuric Acid (TCCA) is one of the suitable alternatives to Gas chlorine. TCCA is a chlorine stabilized compound, stabilized with Cyanuric acid, thus similar to Gas Chlorine in its functions except that it is available in solid form. Release of chlorine is a gradual process in TCCA unlike Gaseous chlorine. Field studies with TCCA indicated gradual and near uniform release rate of chlorine, for longer duration with the requisite free residual chlorine levels (FRC). Thus, use of TCCA could be considered as a suitable alternative for gas chlorine for regular chlorination requirements. (author)

  19. Polycyclic aromatic hydrocarbon in urban soils of an Eastern European megalopolis: distribution, source identification and cancer risk evaluation

    Science.gov (United States)

    Shamilishvily, George; Abakumov, Evgeny; Gabov, Dmitriy

    2018-05-01

    This study explores qualitative and quantitative composition of 15 priority polycyclic aromatic hydrocarbons (PAHs) in urban soils of some parkland, residential and industrial areas of the large industrial centre of Saint Petersburg (Russian Federation) in Eastern Europe. The aim of the study was to test the hypothesis on the PAH loading differences among urban territories with different land use scenarios. Benzo(a)pyrene toxic equivalency factors (TEFs) were used to calculate BaPeq in order to evaluate carcinogenic risk of soil contamination with PAHs. Results of the study demonstrated that soils within residential and industrial areas are characterized by common loads of PAHs generally attributed to high traffic activity in the city. Considerable levels of soil contamination with PAHs were noted. Total PAH concentrations ranged from 0.33 to 8.10 mg kg-1. A larger portion of high-molecular-weight PAHs along with determined molecular ratios suggest the predominance of pyrogenic sources, mainly attributed to combustion of gasoline, diesel and oil. Petrogenic sources of PAHs have a significant portion and define the predominance of low-molecular-weight PAHs associated with petroleum, such as phenanthrene. Derived concentrations of seven carcinogenic PAHs as well as calculated BaPeq were multiple times higher than reported in a number of other studies. The obtained BaPeq concentrations of the sum of 15 PAHs ranged from 0.05 to 1.39 mg kg-1. A vast majority of examined samples showed concentrations above the safe value of 0.6 mg kg-1 (CCME, 2010). However, estimated incremental lifetime risks posed to the population through distinct routes of exposure were in an acceptable range. One-way ANOVA results showed significant differences in total PAHs and the sum of seven carcinogenic PAH concentrations as well as in levels of FLU, PHE, FLT, PYR, BaA, CHR, BbF, BaP and BPE among parkland, residential and industrial land uses, suggesting the influence of the land use factor.

  20. Evaluation of hydrocarbons and organochlorine pesticides and their tolerant microorganisms from an agricultural soil to define its bioremediation feasibility.

    Science.gov (United States)

    Islas-García, Alejandro; Vega-Loyo, Libia; Aguilar-López, Ricardo; Xoconostle-Cázares, Beatriz; Rodríguez-Vázquez, Refugio

    2015-01-01

    The concentrations of hydrocarbons and organochlorine pesticides (OCPs), nutrients and tolerant microorganisms in an agricultural soil from a locality in Tepeaca, Puebla, Mexico, were determined to define its feasibility for bioremediation. The OCPs detected were heptachlor, aldrin, trans-chlordane, endosulfán I, endosulfán II, 1,1,1-bis-(4-chlorophenyl)-2,2-trichloroethane (4,4'-DDT), 1,1-bis-(4-chlorophenyl)-2,2-dichloroethene (4,4'-DDE) and endrin aldehyde, with values of 0.69-30.81 ng g(-1). The concentration of hydrocarbons in the soil of Middle Hydrocarbons Fraction (MHF), C10 to C28, was 4608-27,748 mg kg(-1) and 1117-19,610 mg kg(-1) for Heavy Hydrocarbons Fraction (HHF), C28 to C35, due to an oil spill from the rupture of a pipeline. The soil was deficient in nitrogen (0.03-0.07%) and phosphorus (0 ppm), and therefore it was advisable to fertilize to bio-stimulate the native microorganisms of soil. In the soil samples, hydrocarbonoclast fungi 3.72 × 10(2) to 44.6 × 10(2) CFU g(-1) d.s. and hydrocarbonoclast bacteria (0.17 × 10(5) to 8.60 × 10(5) CFU g(-1) d.s.) were detected, with a tolerance of 30,000 mg kg(-1) of diesel. Moreover, pesticideclast fungi (5.13 × 10(2) to 42.2 × 10(2) CFU g(-1) d.s.) and pesticideclast bacteria (0.15 × 10(5) to 9.68 × 10(5) CFU g(-1) d.s.) were determined with tolerance to 20 mg kg(-1) of OCPs. Fungi and bacteria tolerant to both pollutants were also quantified. Therefore, native microorganisms had potential to be stimulated to degrade hydrocarbons and pesticides or both pollutants. The concentration of pollutants and the microbial activity analyzed indicated that bioremediation of the soil contaminated with hydrocarbons and pesticides using bio-stimulation of native microorganisms was feasible.

  1. Identification of irradiation treatment in processed food. Pt. 2. Evaluation of a SPE-method for analyzing irradiation induced hydrocarbons

    International Nuclear Information System (INIS)

    Hartmann, M.; Ammon, J.; Berg, H.

    1996-01-01

    This paper deals with a solid phase extraction (SPE) method for the isolation of irradiation induced hydrocarbons which can replace the column chromatography described in the paragraph 35 LMBG (German Food Law) procedure L06.00-37. Using this new method, only a tenth of solvents and column material is necessary. The SPE method was a good as LC-LC-GC/FID or LC-LC-GC/MS in analyzing new or complex matrices like paprika or salmon. Additionally, it is fast, cheap and easy to perform. As far as we know, the detection of irradiation traetment in paprika powder by analyzing irradiation induced hydrocarbons has not been described before. The new method is a good alternative for the commonly used thermoluminescence procedure. (orig.) [de

  2. Control of fouling organisms in estuarine cooling water systems by chlorine and bromine chloride

    International Nuclear Information System (INIS)

    Burton, D.T.; Margrey, S.L.

    1979-01-01

    The study described was initiated to evaluate the antifouling effectiveness of chlorine and bromine chloride in low velocity flow areas where estuarine waters are used for cooling purposes. The relative antifouling effectiveness of chlorine and bromine chloride under intermittent and continuous modes of application in low velocity flow areas was evaluated at an estuarine power plant located on the Chesapeake Bay

  3. Evaluation of the phototoxicity of unsubstituted and alkylated polycyclic aromatic hydrocarbons to mysid shrimp (Americamysis bahia): Validation of predictive models.

    Science.gov (United States)

    Finch, Bryson E; Marzooghi, Solmaz; Di Toro, Dominic M; Stubblefield, William A

    2017-08-01

    Crude oils are composed of an assortment of hydrocarbons, some of which are polycyclic aromatic hydrocarbons (PAHs). Polycyclic aromatic hydrocarbons are of particular interest due to their narcotic and potential phototoxic effects. Several studies have examined the phototoxicity of individual PAHs and fresh and weathered crude oils, and several models have been developed to predict PAH toxicity. Fingerprint analyses of oils have shown that PAHs in crude oils are predominantly alkylated. However, current models for estimating PAH phototoxicity assume toxic equivalence between unsubstituted (i.e., parent) and alkyl-substituted compounds. This approach may be incorrect if substantial differences in toxic potency exist between unsubstituted and substituted PAHs. The objective of the present study was to examine the narcotic and photo-enhanced toxicity of commercially available unsubstituted and alkylated PAHs to mysid shrimp (Americamysis bahia). Data were used to validate predictive models of phototoxicity based on the highest occupied molecular orbital-lowest unoccupied molecular orbital (HOMO-LUMO) gap approach and to develop relative effect potencies. Results demonstrated that photo-enhanced toxicity increased with increasing methylation and that phototoxic PAH potencies vary significantly among unsubstituted compounds. Overall, predictive models based on the HOMO-LUMO gap were relatively accurate in predicting phototoxicity for unsubstituted PAHs but are limited to qualitative assessments. Environ Toxicol Chem 2017;36:2043-2049. © 2017 SETAC. © 2017 SETAC.

  4. Evaluating the impact of extraction and cleanup parameters on the yield of total petroleum hydrocarbons in soil

    Energy Technology Data Exchange (ETDEWEB)

    Saari, Eija; Peraemaeki, Paavo; Jalonen, Jorma [University of Oulu, Department of Chemistry (Finland)

    2008-11-15

    Interlaboratory comparisons for the analysis of mineral oil in polluted soil using the GC-FID method indicate that extraction and cleanup conditions have significant effects on the analytical results. In this investigation a ruggedness test was performed on the extraction and cleanup method for the determination of total petroleum hydrocarbons in soil. A two-level Plackett-Burman design was utilized to study the effect of 11 different method parameters on the extraction recovery of total petroleum hydrocarbons (TPH) in soil. Both qualitative and quantitative factors were investigated. The results indicate that total petroleum hydrocarbons can be relatively reliably monitored through strict implementation of the ISO and CEN draft standards. However, variation in certain method parameters readily affects the validity of the results. The most critical factors affecting TPH recovery were the solvent and co-solvent used for extraction, the extraction time, adsorbent and its weight and sample TPH concentration. Because adaptation of the draft standards especially with respect to these factors easily leads to TPH recoveries higher than 200% or lower than 70%, the validity of the adapted method should always be verified. A proper estimate of the expanded uncertainty should also be appended to TPH results, because only then can the reliability of the results be guaranteed and further justification is gained to support the end-use of the data. This also supports the credibility of the analytical services and prevents the data end-users from drawing misleading conclusions concerning the environmental risks and potential remediation requirements. (orig.)

  5. Photodynamic tissue adhesion with chlorin(e6) protein conjugates.

    Science.gov (United States)

    Khadem, J; Veloso, A A; Tolentino, F; Hasan, T; Hamblin, M R

    1999-12-01

    To test the hypothesis that a photodynamic laser-activated tissue solder would perform better in sealing scleral incisions when the photosensitizer was covalently linked to the protein than when it was noncovalently mixed. Conjugates and mixtures were prepared between the photosensitizer chlorin(e6) and various proteins (albumin, fibrinogen, and gelatin) in different ratios and used to weld penetrating scleral incisions made in human cadaveric eyes. A blue-green (488-514 nm) argon laser activated the adhesive, and the strength of the closure was measured by increasing the intraocular pressure until the wound showed leakage. Both covalent conjugates and noncovalent mixtures showed a light dose-dependent increase in leaking pressure. A preparation of albumin chlorin(e6) conjugate with additional albumin added (2.5 protein to chlorin(e6) molar ratio) showed significantly higher weld strength than other protein conjugates and mixtures. This is the first report of dye-protein conjugates as tissue solders. These conjugates may have applications in ophthalmology.

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

    Directory of Open Access Journals (Sweden)

    Elena O Omarova

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

  7. Application of Chlorine-Assisted Chemical Vapor Deposition of Diamond at Low Temperatures

    Science.gov (United States)

    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.

  8. Grundfoss: Chlorination of Swimming Pools

    DEFF Research Database (Denmark)

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

    1998-01-01

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

  9. Hydrocarbon oils

    Energy Technology Data Exchange (ETDEWEB)

    Foorwood, G F; Taplay, J G

    1916-12-12

    Hydrocarbon oils are hydrogenated, cracked, or treated for the removal of sulfur by bringing their vapors mixed with steam at temperatures between 450 and 600/sup 0/C into contact with a form of carbon that is capable of decomposing steam with the production of nascent hydrogen at those temperatures. The forms of carbon used include lamp-black, soot, charcoals derived from wood, cellulose, and lignite, and carbons obtained by carbonizing oil residues and other organic bodies at temperatures below 600/sup 0/C. The process is applied to the treatment of coal oil, shale oil, petroleum, and lignite oil. In examples, kerosene is cracked at 570/sup 0/C, cracked spirit is hydrogenated at 500/sup 0/C, and shale spirit is desulfurized at 530/sup 0/C. The products are led to a condenser and thence to a scrubber, where they are washed with creosote oil. After desulfurization, the products are washed with dilute caustic soda to remove sulfurretted hydrogen.

  10. Hydrocarbon exploration

    Energy Technology Data Exchange (ETDEWEB)

    Lerche, I. (South Carolina Univ., Columbia, SC (United States). Dept. of Geological Sciences)

    1993-01-01

    This special issue of the journal examines various aspects of the on-going search for hydrocarbons, ranging from frontier basins where little data are available, to more mature areas where considerable data are available. The incentives underlying the search for oil are roughly: the social, economic and industrial needs of a nation; the incentive of a corporation to be profitable; and the personal incentives of individuals in the oil industry and governments, which range from financial wealth to power and which are as diverse as the individuals who are involved. From a geopolitical perspective, the needs, requirements, goals, strategies, and philosophies of nations, and groups of nations, also impact on the oil exploration game. Strategies that have been employed have ranged from boycott to austerity and rationing, to physical intervention, to global ''flooding'' with oil by over-production. (author)

  11. Chlorination of uranium oxides in melts of alkali metal chlorides and their mixtures

    International Nuclear Information System (INIS)

    Vorobej, M.P.; Bevz, A.S.; Skiba, O.V.

    1978-01-01

    Chlorination of UO 2 , U 3 O 8 , and UO 3 in melts of chlorides of alkali metals and of their mixtures has been studied by thermogravimetric, X-ray phase, and spectrophotometric methods. The thermogravimetric method has been proposed for evaluating the state of uranylcation in the melt; the effect of the composition of the oxide being chlorinated and of the salt-solvent on the composition of the chlorination products has been studied. The effect of the composition of the chlorination products on the stoichiometry of the electrolytic uranium dioxide has been shown

  12. Quantitative evaluation of volatile hydrocarbons in post-mortem blood in forensic autopsy cases of fire-related deaths.

    Science.gov (United States)

    Yonemitsu, Kosei; Sasao, Ako; Oshima, Toru; Mimasaka, Sohtaro; Ohtsu, Yuki; Nishitani, Yoko

    2012-04-10

    Volatile hydrocarbons in post-mortem blood from victims of fires were analyzed quantitatively by headspace gas chromatography mass spectrometry. The benzene and styrene concentrations in the blood were positively correlated with the carboxyhemoglobin (CO-Hb) concentration, which is evidence that the deceased inhaled the hydrocarbons and carbon monoxide simultaneously. By contrast, the concentrations of toluene and CO-Hb in the blood were not significantly correlated. This lack of correlation could be explained by two different sources of toluene, with low blood concentrations of toluene arising when the deceased inhaled smoke and high blood concentrations of toluene arising when the deceased inhaled petroleum vapor or other unknown vapors. The quantity of soot deposited in the respiratory tract was classified into four grades (-, 1+, 2+, 3+). The mean CO-Hb concentration in the 1+ soot group was significantly lower than those in the 2+ (ptypes of smoke produced by different materials. For example, petroleum combustion with a limited supply of oxygen, like in a compartment fire, may produce a large volume of dense black smoke that contains a large quantity of soot. Soot deposits in the airways and the blood CO-Hb concentration are basic and essential autopsy findings that are used to investigate fire-related deaths. The quantitative GC-MS analysis of blood volatile hydrocarbons can provide additional useful information on the cause of the fire and the circumstances surrounding the death. In combination, these three findings are useful for the reconstruction of cases. Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.

  13. Oak Ridge K-25 Site chlorinated solvent pollution prevention opportunity assessment

    International Nuclear Information System (INIS)

    1994-08-01

    A pollution prevention opportunity assessment (PPOA) was conducted at the Oak Ridge K-25 Site to identify opportunities to reduce and better manage the use of chlorinated solvents. At the K-25 Site, 67 control areas were examined for their potential use of chlorinated solvents. Of these areas, 27 were found to be using (1) chlorinated solvents for cleaning, degreasing, and lubricating; (2) laboratory standards and solvents; and (3) test medium. Current management practices encourage the identification and use of nonhazardous chemicals, including the use of chlorinated solvents. The main pollution prevention principles are source reduction and recycling, and a number of pollution prevention options based on these principles were identified and evaluated as part of this chlorinated solvent PPOA. Source reduction options evaluated for the K-25 Site include the substitution of chlorinated solvents with nonchlorinated solvents. Recycling was identified for those areas that would benefit most from the reuse of the chlorinated solvents in use. The pollution prevention options that offer the greatest opportunity for success at the K-25 Site are the implementation of substitutes at the 10 control areas using chlorinated solvents for cleaning, degreasing, and lubrication. A change in the process may be all that is needed to eliminate the use of a chlorinated solvent. Once a decision is made to implement a substitution, the information should be communicated to all shops and laboratories. Another option to consider is the installation of recycling units to recycle the large amounts of methylene chloride used in the analytical sampling procedure

  14. Oak Ridge K-25 Site chlorinated solvent pollution prevention opportunity assessment

    Energy Technology Data Exchange (ETDEWEB)

    1994-08-01

    A pollution prevention opportunity assessment (PPOA) was conducted at the Oak Ridge K-25 Site to identify opportunities to reduce and better manage the use of chlorinated solvents. At the K-25 Site, 67 control areas were examined for their potential use of chlorinated solvents. Of these areas, 27 were found to be using (1) chlorinated solvents for cleaning, degreasing, and lubricating; (2) laboratory standards and solvents; and (3) test medium. Current management practices encourage the identification and use of nonhazardous chemicals, including the use of chlorinated solvents. The main pollution prevention principles are source reduction and recycling, and a number of pollution prevention options based on these principles were identified and evaluated as part of this chlorinated solvent PPOA. Source reduction options evaluated for the K-25 Site include the substitution of chlorinated solvents with nonchlorinated solvents. Recycling was identified for those areas that would benefit most from the reuse of the chlorinated solvents in use. The pollution prevention options that offer the greatest opportunity for success at the K-25 Site are the implementation of substitutes at the 10 control areas using chlorinated solvents for cleaning, degreasing, and lubrication. A change in the process may be all that is needed to eliminate the use of a chlorinated solvent. Once a decision is made to implement a substitution, the information should be communicated to all shops and laboratories. Another option to consider is the installation of recycling units to recycle the large amounts of methylene chloride used in the analytical sampling procedure.

  15. Predicting hydrocarbon release from soil

    International Nuclear Information System (INIS)

    Poppendieck, D.; Loehr, R.C.

    2002-01-01

    'Full text:' The remediation of hazardous chemicals from soils can be a lengthy and costly process. As a result, recent regulatory initiatives have focused on risk-based corrective action (RBCA) approaches. Such approaches attempt to identify the amount of chemical that can be left at a site with contaminated soil and still be protective of human health and the environment. For hydrocarbons in soils to pose risk to human heath and the environment, the hydrocarbons must be released from the soil and accessible to microorganisms, earthworms, or other higher level organisms. The sorption of hydrocarbons to soil can reduce the availability of the hydrocarbon to receptors. Typically in soils and sediments, there is an initial fast release of a hydrocarbon from the soil to the aqueous phase followed by a slower release of the remaining hydrocarbon to the aqueous phase. The rate and extent of slow release can influence aqueous hydrocarbon concentrations and the fate and transport of hydrocarbons in the subsurface. Once the fast fraction of the chemical has been removed from the soil, the remaining fraction of a chemical may desorb at a rate that natural mechanisms can attenuate the released hydrocarbon. Hence, active remediation may be needed only until the fast fraction has been removed. However, the fast fraction is a soil and chemical specific parameter. This presentation will present a tier I type protocol that has been developed to quickly estimate the fraction of hydrocarbons that are readily released from the soil matrix to the aqueous phase. Previous research in our laboratory and elsewhere has used long-term desorption (four months) studies to determine the readily released fraction. This research shows that a single short-term (less than two weeks) batch extraction procedure provides a good estimate of the fast released fraction derived from long-term experiments. This procedure can be used as a tool to rapidly evaluate the release and bioavailability of

  16. Evaluation of gastrointestinal solubilization of petroleum hydrocarbon residues in soil using an in vitro physiologically based model.

    Science.gov (United States)

    Holman, Hoi-Ying N; Goth-Goldstein, Regine; Aston, David; Yun, Mao; Kengsoontra, Jenny

    2002-03-15

    Petroleum hydrocarbon residues in weathered soils may pose risks to humans through the ingestion pathway. To understand the factors controlling their gastrointestinal (GI) absorption, a newly developed experimental extraction protocol was used to model the GI solubility of total petroleum hydrocarbon (TPH) residues in highly weathered soils from different sites. The GI solubility of TPH residues was significantly higher for soil contaminated with diesel than with crude oil. Compared to the solubility of TPH residues during fasted state,the solubility of TPH residues during fat digestion was much greater. Diesel solubility increased from an average of 8% during the "gallbladder empty" phase of fasting (and less than 0.2% during the otherfasting phase) to an average of 16% during fat digestion. For crude oil, the solubility increased from an average of 1.2% during the gallbladder empty phase of fasting (and undetectable during the other fasting phase) to an average of 4.5% during fat digestion. Increasing the concentration of bile salts also increased GI solubility. GI solubility was reduced by soil organic carbon but enhanced by the TPH content.

  17. Characterisation of Chlorine Behavior in French Graphite

    International Nuclear Information System (INIS)

    Blondel, A.; Moncoffre, N.; Toulhoat, N.; Bererd, N.; Petit, L.; Laurent, G.; Lamouroux, C.

    2016-01-01

    Chlorine 36 is one of the main radionuclides of concern for French graphite waste disposal. In order to help the understanding of its leaching behaviour under disposal conditions, the respective impact of temperature, irradiation and gas radiolysis on chlorine release in reactor has been studied. Chlorine 36 has been simulated through chlorine 37 ion implantation in virgin nuclear graphite samples. Results show that part of chlorine is highly mobile in graphite in the range of French reactors operating temperatures in relation with graphite structural recovering. Ballistic damage generated by irradiation also promotes chlorine release whereas no clear impact of the coolant gas radiolysis was observed in the absence of graphite radiolytic corrosion. (author)

  18. Modeling potential migration of petroleum hydrocarbons from a mixed-waste disposal site in the vadose zone

    International Nuclear Information System (INIS)

    Rawson, S.A.; Walton, J.C.; Baca, R.G.

    1989-01-01

    Environmental monitoring of a mixed-waste disposal site at the Idaho National Engineering Laboratory has confirmed release and migration into the vadose zone of: (1) chlorinated hydrocarbons in the vapor phase and (2) trace levels of certain transuranic elements. The finding has prompted an evaluation of the potential role of waste petroleum hydrocarbons in mediating or influencing contaminant migration from the disposal site. Disposal records indicate that a large volume of machine oil contaminated with transuranic isotopes was disposed at the site along with the chlorinated solvents and other radioactive wastes. A multiphase flow model was used to assess the possible extent of oil and vapor movement through the 177 m thick vadose zone. One dimensional simulations were performed to estimate the vertical distribution of the vapor phase, the aqueous phase, and immiscible free liquid as a function of time. The simulations indicate that the oil may migrate slowly through the vadose zone, to potentially significant depths. Calculated transport rates support the following ranking with regard to relative mobility: vapor phase > aqueous phase > free liquid. 21 refs., 7 figs., 2 tabs

  19. Handbook for Evaluating Ecological Effects of Pollution at DARCOM installations. Volume 2, Essential Background Data. (Installation Environmental Impact Assessment)

    Science.gov (United States)

    1979-12-01

    Nitrates Sulfur dioxide Xylene Nitrites Oxides of nitrogen Mercaptans "Red Water" Carbon monoxide Chlorine Acids: Ketones Fluorine Hydrochloric Esters...Trichloroethylene Varnishes Methylchloroform Undercoatings Mineral spirits Liquid styrene Naphtha Adhesives Halgenated hydrocarbons Nonmethane hydrocarbons

  20. Short-term organic carbon migration from polymeric materials in contact with chlorinated drinking water.

    Science.gov (United States)

    Mao, Guannan; Wang, Yingying; Hammes, Frederik

    2018-02-01

    Polymeric materials are widely used in drinking water distribution systems. These materials could release organic carbon that supports bacterial growth. To date, the available migration assays for polymeric materials have not included the potential influence of chlorination on organic carbon migration behavior. Hence, we established a migration and growth potential protocol specifically for analysis of carbon migration from materials in contact with chlorinated drinking water. Four different materials were tested, including ethylene propylene dienemethylene (EPDM), poly-ethylene (PEX b and PEX c) and poly-butylene (PB). Chlorine consumption rates decreased gradually over time for EPDM, PEXc and PB. In contrast, no free chlorine was detected for PEXb at any time during the 7 migration cycles. Total organic carbon (TOC) and assimilable organic carbon (AOC) was evaluated in both chlorinated and non-chlorinated migrations. TOC concentrations for EPDM and PEXb in chlorinated migrations were significantly higher than non-chlorinated migrations. The AOC results showed pronounced differences among tested materials. AOC concentrations from chlorinated migration waters of EPDM and PB were higher compared to non-chlorinated migrations, whereas the opposite trend was observed for PEXb and PEXc. There was also a considerable difference between tested materials with regards to bacterial growth potential. The results revealed that the materials exposed to chlorine-influenced migration still exhibited a strong biofilm formation potential. The overall results suggested that the choice in material would make a considerable difference in chlorine consumption and carbon migration behavior in drinking water distribution systems. Copyright © 2017 Elsevier B.V. All rights reserved.

  1. Evaluation of corrosivity of the vapor-phase environments to sterilized water with chlorine; Enso kei mekkin shorisui no kisho kankyo no fushokusei

    Energy Technology Data Exchange (ETDEWEB)

    Nakata, Michio. [Nippon Steel Corp. Yamaguchi (Japan). Technical Development Bureau

    1999-08-15

    Corrosivity of vapor-phase aenvironments in indoor pool, water thank, and water purification plants was investigated. Sodium hypochlorite (NaClO) was used as a sterilizing agent in indoor pool, while chlorine gas was used in water tank and water purification plants. It was found that Cl{sup -} ion were concentrated in the dew formed in the indoor pool. H{sup +} ions as well as Cl{sup -} ions were accumulated in the dew dormed in the water tank ans water purification plants. Thus, the corrosion condition was varied with the type of sterilizing agents used. Through the investigation of water tanl, the relationship between pH and Cl{sup -} ion concentration was given as follow; pH=-1.09-2.19 log [Cl{sup -}] (mol/L). Corrosivity of vapor-phase enviroments in sterilizing water systems would be characterized by the exstence of oxidizing chemical agents such as ClO{sup -} and HClO, the shift of corrosion potenrial of the thin water film, and the accumulation of H{sup +} and/or Cl{sup -} ions in the dew. (author)

  2. Process for producing chlorinated polyethylene

    International Nuclear Information System (INIS)

    Nose, Shinji; Takayama, Shin-ichi; Kodama, Takashi.

    1970-01-01

    A process for chlorinated polyethylene by the chlorination of an aqueous suspension of polyethylene without the use catalysts is given, using 5-55% by gel content of cross-linked polyethylene powders. The products have favorable material workability, transparency, impact strength and tensile properties. In the case of peroxide cross-linking, a mixture of peroxides with polyethylene must be ground after heat treatment. The polyethylene may preferably have a gel content of 5-55%. The chlorination temperature may be 40 0 C or more, preferably 60 0 to 160 0 C. In one example, high pressure polymerized fine polyethylene powders of 15μ having a density of 0.935 g/cc, a softening point of 114 0 C, an average molecular weight of 35,000 were irradiated in air with 40 Mrad electron beams from a 2 MV Cockcroft-Walton type accelerator at room temperature. The thus irradiated polyethylene had a gel content of 55% and a softening point of 119 0 C. It was chlorinated upto a chlorine content of 33% at 100 0 C. Products were white crystals having a melting point of 122 0 C and a melting heat value of 32 mcal/mg. A sheet formed from this product showed a tensile strength of 280 kg/cm 2 , an elongation of 370% and a hardness of 90. (Iwakiri, K.)

  3. Derivation of validated methods of sampling and analysis for intermediate and final products of the anaerobic material utilization of volatile chlorinated hydrocarbons (LCFC) in groundwater in the context of analyses of contaminated soils; Ableitung validierter Probenahme- und Analysenmethoden fuer Zwischen- und Endprodukte der anaeroben Stoffverwertungsprozesse von Leichtfluechtigen Chlorierten Kohlenwasserstoffen (LCKW) im Grundwasser im Rahmen von Altlastenuntersuchungen

    Energy Technology Data Exchange (ETDEWEB)

    Dorgerloh, Ute; Becker, Roland; Win, Tin [Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin (Germany); Theissen, Hubert [IMAGO GbR (Germany)

    2010-06-17

    The results of the project ''Methods of sampling and analysis of intermediate and final products of the anaerobic degradation of volatile halogenated hydrocarbons in groundwater in frame of analysis of contaminated sites'' of the German Federal States Program ''Water, Soil, Waste'' (Laenderfinanzierungsprogramm ''Wasser, Boden, Luft'') LFP B2.08 are presented in these report. Different methods of sampling and analysis for the determination of hydrogen, methane, ethene and vinyl chloride in groundwater are developed and validated: For the sampling are described and discussed: i. active sampling: purge and sample of water samples and purging of solvated gases in groundwater in gas sampling tubes ii. passive sampling: diffusion sampling in polyethylene diffusion bags (PDB) and plastic syringes as diffusion sampler for solvated gases The use of active (purge and sample, downhole sampler) and passive (diffusion sampling) sampling techniques for the quantification of VOC, ethene, and methane are evaluated from the viewpoint of public authorities and regarding the reproducibility of measurement results. Based on a groundwater contaminated with trichloroethene, 1,2-dichloroethene, and vinyl chloride it is shown that passive sampling is restricted by low groundwater flow and biological activity inside the well casing. Therefore, active sampling is to be preferred in case of unknown or insufficient flow conditions in the aquifer. The methods of chromatography for the determination of the compounds are validated and compared with other appropriate analytical methods: I. Headspace-GC-FID for the determination of methane, ethene and vinyl chloride in water of the purged sample (i) and the water of the PDB (ii) II. Direct injection - GC-PDD for the determination of hydrogen from the collected gas samples of the gas sampling tube (i) and the plastic syringes (ii) The gas chromatographic procedure for vinyl chloride using

  4. Effect of moisture, charge size, and chlorine concentration on PCDD/F emissions from simulated open burning of forest biomass

    Science.gov (United States)

    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...

  5. Comparison of Phytoscreening and Direct-Push- Based Site Investigation at a Rural Megasite Contaminated with Chlorinated Ethenes

    DEFF Research Database (Denmark)

    Rein, Arno; Holm, Olaf; Trapp, Stefan

    2015-01-01

    areas in particular. Here we compare two site screening techniques that can be applied quickly at relatively low cost, namely Direct Push (DP)-based groundwater sampling and tree core sampling. The effectiveness of both methods is compared for a rural megasite contaminated with chlorinated hydrocarbons...

  6. Epidemiological evidence of carcinogenicity of chlorinated organics in drinking water.

    Science.gov (United States)

    Cantor, K P

    1982-12-01

    Concern has recently been voiced over possible chronic toxicity associated with chlorination of public drinking water supplies in the United States. This paper reviews the available evidence and the studies underway to further evaluate hypothesized associations between cancer risk and byproducts of chlorination. Preliminary data from measures of halogenated volatiles and personal exposure histories from respondents in a large epidemiologic study of bladder cancer are presented. These data support the use in epidemiologic studies of categorical measures of exposure and suggest that results from completed case-control studies, based on death certificates, may have underestimated the true risk of exposure to chlorination by-products. The current generation of studies which use a case-control interview design offer many advantages over earlier efforts to evaluate this issue.

  7. Using Ramped Pyrolysis - Gas Chromatography - Mass Spectrometry to Evaluate Petroleum Hydrocarbons Following the Deepwater Horizon Oil Spill

    Science.gov (United States)

    Evans, M.; Rosenheim, B. E.; Bacosa, H. P.; Liu, J.; Liu, Z.

    2016-02-01

    In summer of 2010, the Deepwater Horizon oil spill polluted hundreds of miles of coastline along the Gulf of Mexico. A combination of human-mediated and natural weathering processes then altered the chemical composition (i.e. toxicity) of this spilled crude oil over time and space. One of the most important, yet challenging, aspects of oil spill science is to quantify these chemical changes in natural environments. In this study, we develop ramped pyrolysis - gas chromatography - mass spectrometry (Py-GC-MS) to address this challenge. In this technique, 0.1mg of freeze-dried sample is pyrolyzed over a gradual temperature ramp (50-650°C). The eluded gas is cold-trapped over different thermal ranges (a.k.a. thermal slicing) and each range is individually analyzed via GC-MS, yielding quantifiable, compound-specific results. Py-GC-MS with thermal slicing has never been used for petroleum hydrocarbon analysis, but it has many advantages - it uses minimal sample, is time efficient and does not require sample preparation (minimizing compound loss and increasing the analytical window). During development of this method, we analyzed oiled sediments and tar collected on Grand Isle, Louisiana from 2010-2012. We quantified n-alkane (C10-C38), polycyclic aromatic hydrocarbon (PAH) and hopane content and confirmed these results with traditional solvent extraction, silica gel fractionation and mass spectrometry. Overall, we found rapid depletion of n-alkanes and PAHs (>90% depletion) in all samples within one year of Deepwater Horizon. After this, n-alkanes were almost 100% depleted by 2012, while PAH degradation continued to a maximum total degradation of 99% and 98% in sediment and tar, respectively. This not only describes the fate of petroleum compounds in salt marshes and beach deposits over time, but also complements previous radiocarbon studies of the same samples showing different rates of degradation in different micro-environments. In addition, the results presented

  8. Analytical evaluation of BEA zeolite for the pre-concentration of polycyclic aromatic hydrocarbons and their subsequent chromatographic analysis in water samples.

    Science.gov (United States)

    Wilson, Walter B; Costa, Andréia A; Wang, Huiyong; Dias, José A; Dias, Sílvia C L; Campiglia, Andres D

    2012-07-06

    The analytical performance of BEA - a commercial zeolite - is evaluated for the pre-concentration of fifteen Environmental Protection Agency - polycyclic aromatic hydrocarbons and their subsequent HPLC analysis in tap and lake water samples. The pre-concentration factors obtained with BEA have led to a method with excellent analytical figures of merit. One milliliter aliquots were sufficient to obtain excellent precision of measurements at the parts-per-trillion concentration level with relative standard deviations varying from 4.1% (dibenzo[a,h]anthracene) to 13.4% (pyrene). The limits of detection were excellent as well and varied between 1.1 (anthracene) and 49.9 ng L(-1) (indeno[1,2,3-cd]pyrene). The recovery values of all the studied compounds meet the criterion for regulated polycyclic aromatic hydrocarbons, which mandates relative standard deviations equal or lower than 25%. The small volume of organic solvents (100 μL per sample) and amount of BEA (2 mg per sample) makes sample pre-concentration environmentally friendly and cost effective. The extraction procedure is well suited for numerous samples as the small working volume (1 mL) facilitates the implementation of simultaneous sample extraction. These are attractive features when routine monitoring of numerous samples is contemplated. Copyright © 2012 Elsevier B.V. All rights reserved.

  9. Detection of chlorinated aromatic compounds

    Science.gov (United States)

    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.

  10. Effects of Chlorine on Enterovirus RNA Degradation

    Science.gov (United States)

    The primary mechanism of disinfection of waterborne pathogens by chlorine has always been believed to be due to the alteration of proteins by free chlorine and subsequent disruption of their biological structure.

  11. Kinetics of molybdenum and chlorine interaction

    International Nuclear Information System (INIS)

    Zelikman, A.N.; Nazarov, Yu.N.; Sarkarov, T.Eh.; Tulyakov, N.V.

    1977-01-01

    The kinetics is studied of molybdenite chlorination with gaseous chlorine. The time dependences of the depth and degree of molybdenite chlorination are given along with the dependence on chlorine concentration of molybdenite chlorination rate. Active interaction is shown to take place at 450-470 deg C. At 350-435 deg C, chlorination occurs in the kinetic range, the apparent activation energy being equal to 22.2 kcal/mole and the order of reaction by chlorine to 0.77. At 435-610 deg C, the process takes place in the diffusion range and is restricted by dissipation of the reaction products (activation energy - 4.05 kcal/mole; order of reaction by chlorine - 0.6)

  12. Formation of aryl-chlorinated aromatic acids and precursors for chloroform in chlorination of humic acid

    NARCIS (Netherlands)

    Sinninghe Damsté, J.S.; Leer, E.W.B. de; Galan, L.

    1985-01-01

    The formation of chloroform when humic substances are chlorinated is well known. Other chlorinated products that may be formed are chloral, di- and trichloroacetic acid, chlorinated C-4 diacids, and α-chlorinated aliphatic acids. Several of these compounds are formed in molar yields comparable

  13. Reductive dechlorination of chlorinated solvents in landfills

    International Nuclear Information System (INIS)

    Wang, J.Y.; Wu, C.

    2002-01-01

    The use of landfills as an in situ biological treatment system represents an alternative for source area remediation with a significant cost saving. The specific objective of this research is to investigate the intrinsic bioattenuation capacity of the landfill ecosystem for chlorinated aliphatic hydrocarbons (CAHs). The research was conducted in two complementary systems: simulated landfill bioreactors and batch degradation experiment in serum bottles. Refuse samples excavated from a landfill were tested in laboratory bioreactors designed and operated to facilitate refuse decomposition under landfilling conditions. Each bioreactor was operated with leachate recirculation and gas collection. Target CAHs, tetrachloroethene (PCE) and trichloroethene (TCE), were added to selected reactors and maintained at 20 μM each in leachate to simulate the effect of long-term exposure of refuse microorganisms to CAHs on the degradation potential of these chemicals in landfills. At two different stages of refuse decomposition, active refuse decomposition representing young landfills and maturation phase representing aged landfills, anaerobic microbial cultures were derived from selected bioreactors and tested in serum bottles for their abilities to biodegrade target CAHs. Results of this study suggest that landfills have an intrinsic reductive dechlorination capacity for PCE and TCE. The decomposition of refuse, a source of complex organics, enhances reductive dechlorination by the refuse cultures tested in this study. In addition, the test results suggest that it may be possible to develop engineering strategies to promote both CAHs degradation and refuse decomposition in landfills. (author)

  14. Direct Chlorination of Zircon Sand

    International Nuclear Information System (INIS)

    Dwiretnani Sudjoko; Budi Sulistyo; Pristi Hartati; Sunardjo

    2002-01-01

    It was investigated the direct chlorination of zircon sand in a unit chlorination equipment. The process was in semi batch. The product gas was scrubbed in aqueous NaOH. It was search the influence of time, ratio of reactant and size of particle sand to the concentration of Zr and Si in the product. From these research it was found that as the times, ratio of reactant increased, the concentration of Zr increased, but the concentration of Si decreased, while as grain size of zircon sand decreased the concentration of Zr decreased, but the concentration of Si increased. (author)

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

    Science.gov (United States)

    Mathieu, Laurence; Francius, Grégory; El Zein, Racha; Angel, Edith; Block, Jean-Claude

    2016-09-01

    The short-term kinetics of bacterial repopulation were evaluated after chlorination of high-density polyethylene (HDPE) colonized with drinking water biofilms and compared with bare HDPE surfaces. The effect of chlorination was partial as a residual biofilm persisted and was time-limited as repopulation occurred immediately after water resupply. The total number of bacteria reached the same levels on both the bare and chlorinated biofilm-fouled HDPE after a seven-day exposure to drinking water. Due to the presence of a residual biofilm, the hydrophobicity of chlorinated biofilm-fouled surface exhibited much lower adhesion forces (2.1 nN) compared to bare surfaces (8.9 nN). This could explain the rapid repopulation after chlorination, with a twofold faster bacterial accumulation rate on the bare HDPE surface. γ-Proteobacteria dominated the early stages of repopulation of both surfaces and a shift in the dominance occurred over the colonization time. Such observations define a timescale for cleaning frequency in industrial environments and guidelines for a rinsing procedure using drinking water.

  16. Real-time drilling mud gas monitoring for qualitative evaluation of hydrocarbon gas composition during deep sea drilling in the Nankai Trough Kumano Basin.

    Science.gov (United States)

    Hammerschmidt, Sebastian B; Wiersberg, Thomas; Heuer, Verena B; Wendt, Jenny; Erzinger, Jörg; Kopf, Achim

    2014-01-01

    Integrated Ocean Drilling Program Expedition 338 was the second scientific expedition with D/V Chikyu during which riser drilling was conducted as part of the Nankai Trough Seismogenic Zone Experiment. Riser drilling enabled sampling and real-time monitoring of drilling mud gas with an onboard scientific drilling mud gas monitoring system ("SciGas"). A second, independent system was provided by Geoservices, a commercial mud logging service. Both systems allowed the determination of (non-) hydrocarbon gas, while the SciGas system also monitored the methane carbon isotope ratio (δ(13)CCH4). The hydrocarbon gas composition was predominated by methane (> 1%), while ethane and propane were up to two orders of magnitude lower. δ(13)CCH4 values suggested an onset of thermogenic gas not earlier than 1600 meter below seafloor. This study aims on evaluating the onboard data and subsequent geological interpretations by conducting shorebased analyses of drilling mud gas samples. During shipboard monitoring of drilling mud gas the SciGas and Geoservices systems recorded up to 8.64% and 16.4% methane, respectively. Ethane and propane concentrations reached up to 0.03 and 0.013%, respectively, in the SciGas system, but 0.09% and 0.23% in the Geoservices data. Shorebased analyses of discrete samples by gas chromatography showed a gas composition with ~0.01 to 1.04% methane, 2 - 18 ppmv ethane, and 2 - 4 ppmv propane. Quadruple mass spectrometry yielded similar results for methane (0.04 to 4.98%). With δD values between -171‰ and -164‰, the stable hydrogen isotopic composition of methane showed little downhole variability. Although the two independent mud gas monitoring systems and shorebased analysis of discrete gas sample yielded different absolute concentrations they all agree well with respect to downhole variations of hydrocarbon gases. The data point to predominantly biogenic methane sources but suggest some contribution from thermogenic sources at depth, probably due

  17. Aspects of chlorination and its potential to produce niobium pentoxide

    International Nuclear Information System (INIS)

    Brocchi, E.A.; Jeffes, J.H.E.

    1984-01-01

    Reduction chlorination of niobium pentoxide were carried out under different experimental conditions in order to study the effects of some variables of the process. In order to evaluate the efficiency of the recovery of niobium pentoxide which could be obtained as condensed material a group of experiments were also carried out with pyrochlore concentrate. The results showed that a balance of factors such as temperature, percentage of carbon in the initial charge and porosity cause the progress of the reaction to be controlled by different mechanisms and indicate that chlorination can be used to produce niobium pentoxide-especially if applied on rich starting material. (Author) [pt

  18. Chlorin photosensitizers sterically designed to prevent self-aggregation.

    Science.gov (United States)

    Uchoa, Adjaci F; de Oliveira, Kleber T; Baptista, Mauricio S; Bortoluzzi, Adailton J; Iamamoto, Yassuko; Serra, Osvaldo A

    2011-11-04

    The synthesis and photophysical evaluation of new chlorin derivatives are described. The Diels-Alder reaction between protoporphyrin IX dimethyl ester and substituted maleimides furnishes endo-adducts that completely prevent the self-aggregation of the chlorins. Fluorescence, resonant light scattering (RLS) and (1)H NMR experiments, as well as X-ray crystallographic have demonstrated that the configurational arrangement of the synthesized chlorins prevent π-stacking interactions between macrocycles, thus indicating that it is a nonaggregating photosensitizer with high singlet oxygen (Φ(Δ)) and fluorescence (Φ(f)) quantum yields. Our results show that this type of synthetic strategy may provide the lead to a new generation of PDT photosensitizers.

  19. Survey of potential chlorine production processes. Final report

    Energy Technology Data Exchange (ETDEWEB)

    1979-04-01

    This report is part of the ongoing study of industrial electrochemical processes for the purpose of identifying methods of improving energy efficiencies. A computerized literature search of past and current chlorine generation methods was performed to identify basic chlorine production processes. Over 200 pertinent references are cited involving 20 separate and distinct chlorine processes. Each basic process is evaluated for its engineering and economic viability and energy efficiency. A flow diagram is provided for each basic process. Four criteria are used to determine the most promising processes: raw material availability, type and amount of energy required, by-product demand/disposal and status of development. The most promising processes are determined to be the membrane process (with and without catalytic electrodes), Kel-Chlor, Mobay (direct electrolysis of hydrogen chloride), the Shell process (catalytic oxidation of hydrogen chloride) and oxidation of ammonium chloride. Each of these processes is further studied to determine what activities may be pursued.

  20. Detection of chlorine in water

    Czech Academy of Sciences Publication Activity Database

    Kašík, Ivan; Mrázek, Jan; Podrazký, Ondřej; Seidl, Miroslav; Aubrecht, Jan; Tobiška, Petr; Pospíšilová, Marie; Matějec, Vlastimil; Kovács, B.; Markovics, A.; Szili, M.

    2009-01-01

    Roč. 139, č. 1 (2009), s. 139-142 ISSN 0925-4005 R&D Projects: GA MŠk(CZ) LC06034; GA ČR(CZ) GA102/05/0948 Institutional research plan: CEZ:AV0Z20670512 Keywords : optical fiber sensor * chlorine Subject RIV: JB - Sensors, Measurment, Regulation Impact factor: 3.083, year: 2009

  1. FTIR analysis and evaluation of carcinogenic and mutagenic risks of nitro-polycyclic aromatic hydrocarbons in PM1.0.

    Science.gov (United States)

    Schneider, Ismael Luís; Teixeira, Elba Calesso; Agudelo-Castañeda, Dayana Milena; Silva E Silva, Gabriel; Balzaretti, Naira; Braga, Marcel Ferreira; Oliveira, Luís Felipe Silva

    2016-01-15

    Nitro-polycyclic aromatic hydrocarbons (NPAHs) represent a group of organic compounds of significant interest due to their presence in airborne particulates of urban centers, wide distribution in the environment, and mutagenic and carcinogenic properties. These compounds, associated with atmospheric particles of size PM1.0) using infrared spectrometry. Carcinogenic and mutagenic risks of the studied NPAHs associated with PM1.0 samples were also determined for two sampling sites: Canoas and Sapucaia do Sul. The results showed that NPAH standard spectra can effectively identify NPAHs in PM1.0 samples. The transmittance and emissivity sample spectra showed broader bands and lower relative intensity than the standard NPAH spectra. The carcinogenic risk and the total mutagenic risk were calculated using the toxic equivalent factors and mutagenic potency factors, respectively. Canoas showed the highest total carcinogenic risk, while Sapucaia do Sul had the highest mutagenic risk. The seasonal analysis suggested that in the study area the ambient air is more toxic during the cold periods. These findings might of significant importance for the decision and policy making authorities.

  2. A critical evaluation of magnetic activated carbon's potential for the remediation of sediment impacted by polycyclic aromatic hydrocarbons.

    Science.gov (United States)

    Han, Zhantao; Sani, Badruddeen; Akkanen, Jarkko; Abel, Sebastian; Nybom, Inna; Karapanagioti, Hrissi K; Werner, David

    2015-04-09

    Addition of activated carbon (AC) or biochar (BC) to sediment to reduce the chemical and biological availability of organic contaminants is a promising in-situ remediation technology. But concerns about leaving the adsorbed pollutants in place motivate research into sorbent recovery methods. This study explores the use of magnetic sorbents. A coal-based magnetic activated carbon (MAC) was identified as the strongest of four AC and BC derived magnetic sorbents for polycyclic aromatic hydrocarbons (PAHs) remediation. An 8.1% MAC amendment (w/w, equal to 5% AC content) was found to be as effective as 5% (w/w) pristine AC in reducing aqueous PAHs within three months by 98%. MAC recovery from sediment after three months was 77%, and incomplete MAC recovery had both, positive and negative effects. A slight rebound of aqueous PAH concentrations was observed following the MAC recovery, but aqueous PAH concentrations then dropped again after six months, likely due to the presence of the 23% unrecovered MAC. On the other hand, the 77% recovery of the 8.1% MAC dose was insufficient to reduce ecotoxic effects of fine grained AC or MAC amendment on the egestion rate, growth and reproduction of the AC sensitive species Lumbriculus variegatus. Copyright © 2014 Elsevier B.V. All rights reserved.

  3. Application of in situ biosparging to remediate a petroleum-hydrocarbon spill site: field and microbial evaluation.

    Science.gov (United States)

    Kao, C M; Chen, C Y; Chen, S C; Chien, H Y; Chen, Y L

    2008-02-01

    In this study, a full-scale biosparging investigation was conducted at a petroleum-hydrocarbon spill site. Field results reveal that natural attenuation was the main cause of the decrease in major contaminants [benzene, toluene, ethylbenzene, and xylenes (BTEX)] concentrations in groundwater before the operation of biosparging system. Evidence of the occurrence of natural attenuation within the BTEX plume includes: (1) decrease of DO, nitrate, sulfate, and redox potential, (2) production of dissolved ferrous iron, sulfide, methane, and CO(2), (3) decreased BTEX concentrations along the transport path, (4) increased microbial populations, and (5) limited spreading of the BTEX plume. Field results also reveal that the operation of biosparging caused the shifting of anaerobic conditions inside the plume to aerobic conditions. This variation can be confirmed by the following field observations inside the plume due to the biosparging process: (1) increase in DO, redox potential, nitrate, and sulfate, (2) decrease dissolved ferrous iron, sulfide, and methane, (3) increased total cultivable heterotrophs, and (4) decreased total cultivable anaerobes as well as methanogens. Results of polymerase chain reaction, denaturing gradient gel electrophoresis, and nucleotide sequence analysis reveal that three BTEX biodegraders (Candidauts magnetobacterium, Flavobacteriales bacterium, and Bacteroidetes bacterium) might exist at this site. Results show that more than 70% of BTEX has been removed through the biosparging system within a 10-month remedial period at an averaged groundwater temperature of 18 degrees C. This indicates that biosparging is a promising technology to remediate BTEX contaminated groundwater.

  4. The evaluation of polycyclic aromatic hydrocarbons (PAHs) biodegradation kinetics in soil amended with organic fertilizers and bulking agents.

    Science.gov (United States)

    Włóka, Dariusz; Placek, Agnieszka; Rorat, Agnieszka; Smol, Marzena; Kacprzak, Małgorzata

    2017-11-01

    The aim of this study was to investigate the polycyclic aromatic hydrocarbons (PAHs) biodegradation kinetics in soils fertilized with organic amendments (sewage sludge, compost), bulking agents (mineral sorbent, silicon dioxide in form of nano powder), and novel compositions of those materials. The scope of conducted works includes a cyclic CO 2 production measurements and the determinations of PAHs content in soil samples, before and after 3-months of incubation. Obtained results show that the use of both type of organic fertilizers have a positive effect on the PAHs removal from soil. However, the CO 2 emission remains higher only in the first stage of the process. The best acquired means in terms of PAHs removal as well as most sustained CO 2 production were noted in samples treated with the mixtures of organic fertilizers and bulking agents. In conclusion the addition of structural forming materials to the organic fertilizers was critical for the soil bioremediation efficiency. Therefore, the practical implementation of collected data could find a wide range of applications during the design of new, more effective solutions for the soil bioremediation purposes. Copyright © 2017 Elsevier Inc. All rights reserved.

  5. Degradation of chloramphenicol by UV/chlorine treatment: Kinetics, mechanism and enhanced formation of halonitromethanes.

    Science.gov (United States)

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

    2017-09-15

    Ultraviolet (UV)/chlorine process is considered as an emerging advanced oxidation process for the degradation of micropollutants. This study investigated the degradation of chloramphenicol (CAP) and formation of disinfection by-products (DBPs) during the UV/chlorine treatment. It was found that CAP degradation was enhanced by combined UV/chlorine treatment compared to that of UV and chlorination treatment alone. The pseudo-first-order rate constant of the UV/chlorine process at pH 7.0 reached 0.016 s -1 , which was 10.0 and 2.0 folds that observed from UV and chlorination alone, respectively. The enhancement can be attributed to the formation of diverse radicals (HO and reactive chlorine species (RCSs)), and the contribution of RCSs maintained more stable than that of HO at pH 5.5-8.5. Meanwhile, enhanced DBPs formation during the UV/chlorine treatment was observed. Both the simultaneous formation and 24-h halonitromethanes formation potential (HNMsFP) were positively correlated with the UV/chlorine treatment time. Although the simultaneous trichloronitromethane (TCNM) formation decreased with the prolonged UV irradiation, TCNM dominated the formation of HNMs after 24 h (>97.0%). According to structural analysis of transformation by-products, both the accelerated CAP degradation and enhanced HNMs formation steps were proposed. Overall, the formation of diverse radicals during the UV/chlorine treatment accelerated the degradation of CAP, while also enhanced the formation of DBPs simultaneously, indicating the need for DBPs evaluation before the application of combined UV/chlorine process. Copyright © 2017 Elsevier Ltd. All rights reserved.

  6. Optimization of Chlorination Process for Mature Leachate Disinfection Using Response Surface Methodology

    Directory of Open Access Journals (Sweden)

    Hamzeh Ali Jamali1

    2014-06-01

    Full Text Available Background: leachate from landfill contains high level of microbial pathogens which is considered as one of the most important threats for the environment. One of the common and simple methods for water and wastewater disinfection is chlorination, but it rarely has been used for leachate disinfection. The objective of this study was evaluating the efficiency of chlorine for leachate disinfection and optimization of the effect of concentration and contact time on the death of total and fecal coliforms, as a microbial contamination index. Methods: In this descriptive-analysis study, microbial indices monitoring in leachates initiated from landfill of Qazvin city were conducted for one year. After pre-tests, the range of chlorine concentration and contact time on the inactivation of microbial indices were determined. Central composite design (CCD and response surface methodology (RSM were applied to optimize chlorine concentration and contact time parameters effect on microbial inactivation. 13 runs of tests were performed on samples. Tests were included BOD, COD, total and fecal coliforms. All analytical experiments were according to the standard methods for the examination of water and wastewater. Results: Results of the study showed that microbial indices had relatively high sensitivity to inactivation by chlorination, which in the chlorine concentration of 2 mg/L and contact time of 9 min, and chlorine concentration of 0.5 mg/L and contact time of 12 min, 100% of total and fecal coliforms inactivated, respectively. The RSM method was used for analysis of bacterial inactivation. Analyses showed that in contact time of 9.4 min and chlorine concentration of 2.99 mg/L, the inactivation efficiency of total and fecal coliforms were 89.16% and 100%, respectively. Conclusions: Chlorine could be used for leachate disinfection. However, in high concentrations of organic matter in leachates, due to production potential of chlorination by-products, health

  7. Converting high boiling hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Terrisse, H; DuFour, L

    1929-02-12

    A process is given for converting high boiling hydrocarbons into low boiling hydrocarbons, characterized in that the high boiling hydrocarbons are heated to 200 to 500/sup 0/C in the presence of ferrous chloride and of such gases as hydrogen, water gas, and the like gases under a pressure of from 5 to 40 kilograms per square centimeter. The desulfurization of the hydrocarbons occurs simultaneously.

  8. Reservoir evaluation of thin-bedded turbidites and hydrocarbon pore thickness estimation for an accurate quantification of resource

    Science.gov (United States)

    Omoniyi, Bayonle; Stow, Dorrik

    2016-04-01

    One of the major challenges in the assessment of and production from turbidite reservoirs is to take full account of thin and medium-bedded turbidites (succession, they can go unnoticed by conventional analysis and so negatively impact on reserve estimation, particularly in fields producing from prolific thick-bedded turbidite reservoirs. Field development plans often take little note of such thin beds, which are therefore bypassed by mainstream production. In fact, the trapped and bypassed fluids can be vital where maximising field value and optimising production are key business drivers. We have studied in detail, a succession of thin-bedded turbidites associated with thicker-bedded reservoir facies in the North Brae Field, UKCS, using a combination of conventional logs and cores to assess the significance of thin-bedded turbidites in computing hydrocarbon pore thickness (HPT). This quantity, being an indirect measure of thickness, is critical for an accurate estimation of original-oil-in-place (OOIP). By using a combination of conventional and unconventional logging analysis techniques, we obtain three different results for the reservoir intervals studied. These results include estimated net sand thickness, average sand thickness, and their distribution trend within a 3D structural grid. The net sand thickness varies from 205 to 380 ft, and HPT ranges from 21.53 to 39.90 ft. We observe that an integrated approach (neutron-density cross plots conditioned to cores) to HPT quantification reduces the associated uncertainties significantly, resulting in estimation of 96% of actual HPT. Further work will focus on assessing the 3D dynamic connectivity of the low-pay sands with the surrounding thick-bedded turbidite facies.

  9. Evaluation of genotoxicity in automobile mechanics occupationally exposed to polycyclic aromatic hydrocarbons using micronuclei and other nuclear abnormalities.

    Science.gov (United States)

    Khan, Mohammed Rafiq; Sudha, Sellappa

    2012-01-01

    Occupational and environmental exposures mostly represent mixtures of genotoxic agents, whereas the specificity of biomarker measurements varies widely. Exploration of correlations among biomarkers contributes to the further progress of molecular cancer epidemiology and to the selection of the optimal biomarkers for the investigation of human exposure to carcinogens. The aim of this study was to assess the potential cytogenetic damage associated with occupational exposure to Polycyclic Aromatic Hydrocarbons (PAHs) among automobile mechanics by using Micronuclei (MN) and other Nuclear Abnormalities (NA) as a biomarker. The study population composed of 110 occupationally exposed automobile mechanics and 100 unexposed controls. All the study participants were males. Both the exposed and control individuals were selected from automobile garages located in the urban area of Coimbatore City, South India. Exfoliated buccal cells were collected from 110 automobile mechanics and 100 age and sex matched controls. Further, cells were examined for MN frequency and Nuclear Abnormalities (NA) other than micronuclei, such as binucleates, broken eggs and karyolysis. Results showed a statistically significant difference between occupationally exposed automobile mechanics and control groups. MN and NA frequencies in automobile mechanics were significantly higher than those in control groups (p < 0.05) and also significantly related to smoking habit (p < 0.05). In addition, a higher degree of NA was observed among the exposed subjects with smoking, drinking, tobacco chewing, which is an indicative of cytogenetic damage in these individuals. MN and other NA reflect genetic changes, events associated with carcinogenesis. Therefore, the results of this study indicate that automobile mechanics exposed to PAHs are under risk of significant cytogenetic damage. Therefore, it is important to provide and offer better awareness of occupational hazards among these workers to promote

  10. Evaluating officially reported polycyclic aromatic hydrocarbon emissions in the Athabasca oil sands region with a multimedia fate model

    Science.gov (United States)

    Parajulee, Abha; Wania, Frank

    2014-01-01

    Emissions of organic substances with potential toxicity to humans and the environment are a major concern surrounding the rapid industrial development in the Athabasca oil sands region (AOSR). Although concentrations of polycyclic aromatic hydrocarbons (PAHs) in some environmental samples have been reported, a comprehensive picture of organic contaminant sources, pathways, and sinks within the AOSR has yet to be elucidated. We sought to use a dynamic multimedia environmental fate model to reconcile the emissions and residue levels reported for three representative PAHs in the AOSR. Data describing emissions to air compiled from two official sources result in simulated concentrations in air, soil, water, and foliage that tend to fall close to or below the minimum measured concentrations of phenanthrene, pyrene, and benzo(a)pyrene in the environment. Accounting for evaporative emissions (e.g., from tailings pond disposal) provides a more realistic representation of PAH distribution in the AOSR. Such indirect emissions to air were found to be a greater contributor of PAHs to the AOSR atmosphere relative to reported direct emissions to air. The indirect pathway transporting uncontrolled releases of PAHs to aquatic systems via the atmosphere may be as significant a contributor of PAHs to aquatic systems as other supply pathways. Emission density estimates for the three PAHs that account for tailings pond disposal are much closer to estimated global averages than estimates based on the available emissions datasets, which fall close to the global minima. Our results highlight the need for improved accounting of PAH emissions from oil sands operations, especially in light of continued expansion of these operations. PMID:24596429

  11. Evaluation of ethyl lactate as solvent in Fenton oxidation for the remediation of total petroleum hydrocarbon (TPH)-contaminated soil.

    Science.gov (United States)

    Jalilian Ahmadkalaei, Seyedeh Pegah; Gan, Suyin; Ng, Hoon Kiat; Abdul Talib, Suhaimi

    2017-07-01

    Due to the health and environmental risks posed by the presence of petroleum-contaminated areas around the world, remediation of petroleum-contaminated soil has drawn much attention from researchers. Combining Fenton reaction with a solvent has been proposed as a novel way to remediate contaminated soils. In this study, a green solvent, ethyl lactate (EL), has been used in conjunction with Fenton's reagents for the remediation of diesel-contaminated soil. The main aim of this research is to determine how the addition of EL affects Fenton reaction for the destruction of total petroleum hydrocarbons (TPHs) within the diesel range. Specifically, the effects of different parameters, including liquid phase volume-to-soil weight (L/S) ratio, hydrogen peroxide (H 2 O 2 ) concentration and EL% on the removal efficiency, have been studied in batch experiments. The results showed that an increase in H 2 O 2 resulted in an increase in removal efficiency of TPH from 68.41% at H 2 O 2  = 0.1 M to 90.21% at H 2 O 2  = 2 M. The lowest L/S, i.e. L/S = 1, had the highest TPH removal efficiency of 85.77%. An increase in EL% up to 10% increased the removal efficiency to 96.74% for TPH, and with further increase in EL%, the removal efficiency of TPH decreased to 89.6%. EL with an optimum value of 10% was found to be best for TPH removal in EL-based Fenton reaction. The power law and pseudo-first order equations fitted well to the experimental kinetic data of Fenton reactions.

  12. Chlorination Revisited: Does Cl- Serve as a Catalyst in the Chlorination of Phenols?

    Science.gov (United States)

    Lau, Stephanie S; Abraham, Sonali M; Roberts, A Lynn

    2016-12-20

    The aqueous chlorination of (chloro)phenols is one of the best-studied reactions in the environmental literature. Previous researchers have attributed these reactions to two chlorine species: HOCl (at circum-neutral and high pH) and H 2 OCl + (at low pH). In this study, we seek to examine the roles that two largely overlooked chlorine species, Cl 2 and Cl 2 O, may play in the chlorination of (chloro)phenols. Solution pH, chloride concentration, and chlorine dose were systematically varied in order to assess the importance of different chlorine species as chlorinating agents. Our findings indicate that chlorination rates at pH pH 6.0 and a chlorine dose representative of drinking water treatment, Cl 2 O is predicted to have at best a minor impact on chlorination reactions, whereas Cl 2 may contribute more than 80% to the overall chlorination rate depending on the (chloro)phenol identity and chloride concentration. While it is not possible to preclude H 2 OCl + as a chlorinating agent, we were able to model our low-pH data by considering Cl 2 only. Even traces of chloride can generate sufficient Cl 2 to influence chlorination kinetics, highlighting the role of chloride as a catalyst in chlorination reactions.

  13. Degradation of acrylamide by the UV/chlorine advanced oxidation process.

    Science.gov (United States)

    Gao, Ze-Chen; Lin, Yi-Li; Xu, Bin; Pan, Yang; Xia, Sheng-Ji; Gao, Nai-Yun; Zhang, Tian-Yang; Chen, Ming

    2017-11-01

    The degradation of acrylamide (AA) during UV/chlorine advanced oxidation process (AOP) was investigated in this study. The degradation of AA was negligible during UV irradiation alone. However, AA could be effectively degraded and mineralized during UV/chlorination due to the generation of hydroxyl radicals (OH). The degradation kinetics of AA during UV/chlorination fitted the pseudo-first order kinetics with the rate constant between AA and OH radicals being determined as 2.11 × 10 9  M -1  s -1 . The degradation rate and mineralization of AA during UV/chlorination were significantly promoted at acidic conditions as well as increasing chlorine dosage. The volatile degradation products of AA during UV/chlorination were identified using gas chromatography-mass spectrometry and the degradation pathways were then proposed accordingly. The formation of disinfection by-products (DBPs) in Milli-Q water and tap water during UV/chlorination of AA was also investigated. The DBPs included chloroform, dichloroacetonitrile, trichloroacetonitrile, 2,2-dichloroacetamide and 2,2,2-trichloroacetamide. Furthermore, the variations of AA degradation during UV/chlorination in different real water samples were evaluated. Copyright © 2017 Elsevier Ltd. All rights reserved.

  14. Chlorine disinfection of dye wastewater: Implications for a commercial azo dye mixture

    Energy Technology Data Exchange (ETDEWEB)

    Vacchi, Francine Inforcato; Albuquerque, Anjaina Fernandes; Vendemiatti, Josiane Aparecida; Morales, Daniel Alexandre [Faculdade de Tecnologia, Universidade Estadual de Campinas, Limeira, SP, 13484-332 (Brazil); Ormond, Alexandra B.; Freeman, Harold S. [Department of Textile Engineering, Chemistry, and Science, North Carolina State University, Raleigh, NC 27695-8301 (United States); Zocolo, Guilherme Juliao; Zanoni, Maria Valnice Boldrin [Departamento de Quimica Analitica, Universidade Estadual Paulista Julio de Mesquita Filho, Instituto de Quimica de Araraquara, Araraquara, SP 14801-970 (Brazil); Umbuzeiro, Gisela, E-mail: giselau@ft.unicamp.br [Faculdade de Tecnologia, Universidade Estadual de Campinas, Limeira, SP, 13484-332 (Brazil)

    2013-01-01

    Azo dyes, the most widely used family of synthetic dyes, are often employed as colorants in areas such as textiles, plastics, foods/drugs/cosmetics, and electronics. Following their use in industrial applications, azo dyes have been found in effluents and various receiving waters. Chemical treatment of effluents containing azo dyes includes disinfection using chlorine, which can generate compounds of varying eco/genotoxicity. Among the widely known commercial azo dyes for synthetic fibers is C.I. Disperse Red 1. While this dye is known to exist as a complex mixture, reports of eco/genotoxicity involve the purified form. Bearing in mind the potential for adverse synergistic effects arising from exposures to chemical mixtures, the aim of the present study was to characterize the components of commercial Disperse Red 1 and its chlorine-mediated decoloration products and to evaluate their ecotoxicity and mutagenicity. In conducting the present study, Disperse Red 1 was treated with chlorine gas, and the solution obtained was analyzed with the aid of LC-ESI-MS/MS to identify the components present, and then evaluated for ecotoxicity and mutagenicity, using Daphnia similis and Salmonella/microsome assays, respectively. The results of this study indicated that chlorination of Disperse Red 1 produced four chlorinated aromatic compounds as the main products and that the degradation products were more ecotoxic than the parent dye. These results suggest that a disinfection process using chlorine should be avoided for effluents containing hydrophobic azo dyes such commercial Disperse Red 1. -- Highlights: Black-Right-Pointing-Pointer Aqueous solutions of Disperse Red 1 were treated with chlorine. Black-Right-Pointing-Pointer The chlorination products of Disperse Red 1 were identified using LC-ESI-MS/MS. Black-Right-Pointing-Pointer Daphnia and Salmonella/microsome were employed for eco/genotoxicity testing. Black-Right-Pointing-Pointer The chlorinated dye was more mutagenic

  15. Chlorine disinfection of dye wastewater: Implications for a commercial azo dye mixture

    International Nuclear Information System (INIS)

    Vacchi, Francine Inforçato; Albuquerque, Anjaina Fernandes; Vendemiatti, Josiane Aparecida; Morales, Daniel Alexandre; Ormond, Alexandra B.; Freeman, Harold S.; Zocolo, Guilherme Julião; Zanoni, Maria Valnice Boldrin; Umbuzeiro, Gisela

    2013-01-01

    Azo dyes, the most widely used family of synthetic dyes, are often employed as colorants in areas such as textiles, plastics, foods/drugs/cosmetics, and electronics. Following their use in industrial applications, azo dyes have been found in effluents and various receiving waters. Chemical treatment of effluents containing azo dyes includes disinfection using chlorine, which can generate compounds of varying eco/genotoxicity. Among the widely known commercial azo dyes for synthetic fibers is C.I. Disperse Red 1. While this dye is known to exist as a complex mixture, reports of eco/genotoxicity involve the purified form. Bearing in mind the potential for adverse synergistic effects arising from exposures to chemical mixtures, the aim of the present study was to characterize the components of commercial Disperse Red 1 and its chlorine-mediated decoloration products and to evaluate their ecotoxicity and mutagenicity. In conducting the present study, Disperse Red 1 was treated with chlorine gas, and the solution obtained was analyzed with the aid of LC–ESI-MS/MS to identify the components present, and then evaluated for ecotoxicity and mutagenicity, using Daphnia similis and Salmonella/microsome assays, respectively. The results of this study indicated that chlorination of Disperse Red 1 produced four chlorinated aromatic compounds as the main products and that the degradation products were more ecotoxic than the parent dye. These results suggest that a disinfection process using chlorine should be avoided for effluents containing hydrophobic azo dyes such commercial Disperse Red 1. -- Highlights: ► Aqueous solutions of Disperse Red 1 were treated with chlorine. ► The chlorination products of Disperse Red 1 were identified using LC–ESI-MS/MS. ► Daphnia and Salmonella/microsome were employed for eco/genotoxicity testing. ► The chlorinated dye was more mutagenic than the dye itself. ► Chlorination should be avoided in effluents containing azo-dyes.

  16. Experimental cancer studies of chlorinated by-products

    International Nuclear Information System (INIS)

    Komulainen, Hannu

    2004-01-01

    Chlorinated drinking water contains a number of different by-products formed during the chlorination process from organic matter. The carcinogenicity of only a fraction of them have been evaluated in experimental animals. The focus has been on compounds and groups of compounds that are most abundant in chlorinated drinking water or the in vitro toxicity data have suggested genotoxic potential. From trihalomethanes, chloroform causes liver tumors in mice and female rats and renal tumors in male mice and rats. Tumor formation by chloroform is strongly associated with cytotoxicity and regenerative cell proliferation in tissues and that has been considered to be one determinant of its carcinogenicity. From halogenic acetic acids, dichloroacetic acid (DCA) and trichlotoacetic acid (TCA) are hepatocarcinogenic in mice and DCA in male rats. Their genotoxicity is equivocal and nongenotoxic mechanisms, such as peroxisome proliferation and hypomethylation of DNA in the liver, likely contribute to tumor development. From chlorinated furanones (CHFs), 3-chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone (MX) is a multisite carcinogen in rats (e.g. in thyroid glands and liver) and it has caused DNA damage in vivo. MX may be a complete carcinogen because it also has promoter properties in vitro. Chlorinated drinking water may also contain brominated by-products providing the raw water contains bromide. At least some of them (bromodichloromethane, bromoform) have been shown to be carcinogenic in laboratory animals. Altogether, although several by-products have been shown to have carcinogenic potential in laboratory animals, it not yet possible to state which compounds or groups of by-products cause the cancer risk in chlorinated drinking water. The cellular mechanisms of their effects and these effects at low concentrations are still poorly understood. The few studies with mixtures of these by-products suggest that the mixture effects may be complex and unpredictable (inhibitory

  17. Evaluation of thermal infrared hyperspectral imagery for the detection of onshore methane plumes: Significance for hydrocarbon exploration and monitoring

    Science.gov (United States)

    Scafutto, Rebecca DeĺPapa Moreira; de Souza Filho, Carlos Roberto; Riley, Dean N.; de Oliveira, Wilson Jose

    2018-02-01

    accurately. These results indicate that thermal infrared hyperspectral imaging can support the oil industry profusely, by revealing new petroleum plays through direct detection of gaseous hydrocarbon seepages, serving as tools to monitor leaks along pipelines and oil processing plants, while simultaneously refining estimates of CH4 emissions.

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

    Science.gov (United States)

    Sutter, B.; Archer, D. P.; Ming, D. W.; Niles, P. B.; Eigenbrode, J. L.; Franz, H.; Glavin, D. P.; McAdam, A. C.; Mahaffy, P; Stern, J. C.; hide

    2014-01-01

    The Sample Analysis at Mars (SAM) instrument onboard the Curiosity rover detect-ed O2 and HCl gas releases from the Rocknest (RN) eolian bedform and the John Klein (JK) and Cumberland (CB) drill hole materials in Gale Crater. Chlorinated hydrocarbons have also been detected by the SAM quadrupole mass spectrometer (QMS) and gas chromatography/mass spectrometer (GCMS). These detections along with the detection of perchlorate (ClO4-) by the Mars Phoenix Lander’s Wet Chemistry Laboratory (WCL) suggesting perchlorate is a possible candidate for evolved O2 and chlorine species. Laboratory thermal analysis of perchlorates has yet to provide an unequivocal temperature match to the SAM O2 and HCl release data. Iron mineralogy found in the Rocknest materials when mixed with Ca-perchlorate does cause O2 release temperatures to be closer match to the SAM O2 release data but more work is required in evaluating the catalytic effects of Fe mineralogy on perchlorate decomposition. Chlorates (ClO3-) are relevant Mars materials and potential O2 and Cl sources. The objective of this work is to evaluate the thermal decomposition of select chlorate (ClO3-) salts as possible sources of the O2 and HCl releases in the Gale Crater materials.

  19. Water Chlorination for human consumption

    International Nuclear Information System (INIS)

    Innocenti, A.; Giacosa, D.; Segatori, M.

    1999-01-01

    Beginning from this issue, an initiative of Federgasacqua (Federal association dealing with the gas and the water) takes place through the activities of the Task Forces Water Quality Control and Materials and Processes, which aim is to offer to the water industry operators and updated information concerning some main subjects, emphasizing in particular the technical and management applied topics. The paper deals with the chlorination processes in drinking water treatment. An overview of the italian situation is presented, concerning disinfection as well as other oxidation processes, together with an historical background on chlorination. Concerning the applications, the chemical technologies and the main processes, the disinfectant effectiveness and the byproducts formation have been described. Further, the regulations in force have been reported and discussed on national and international bases [it

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

    Science.gov (United States)

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

    2016-08-01

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

  1. Characterization of hydrocarbon utilizing fungi from hydrocarbon ...

    African Journals Online (AJOL)

    Prof. Ogunji

    isolated fungi could be useful in the bioremediation of hydrocarbon polluted sites. Keywords: ... Technologies such as mechanical force, burying, evaporation, dispersant application, and ..... The effects of drilling fluids on marine bacteria from a.

  2. Metabolic fate of chlorinated paraffins

    International Nuclear Information System (INIS)

    Darnerud, P.O.; Biessmann, A.; Brandt, I.

    1982-01-01

    The disposition of three [1- 14 C]-chlorododecanes (MCDD, PCDD I and PCDD II; 17.4%, 55.9%, and 68.5% chlorination) was studied in C57Bl mice. [1- 14 C]-lauric acid (LA) was studied as reference compound. Fifty-two percent (MCDD), 32% (PCDD I), and 8% (PCDD II) of the radioactive doses were exhaled as 14 CO 2 during 12 h after i.v. injection. Similar results were obtained after p.o. administration. In addition to a marked labelling of the liver and fat, the distribution patterns observed at 24 h after administration revealed an uptake of radioactivity in tissues with high cell turnover/high metabolic activity, e.g., intestinal mucosa, bone marrow, salivary glands and thymus. The concentration of radioactivity in these sites and the exhalation of 14 CO 2 , which were inverse to the degree of chlorination, indicate that the chloroalkanes are degraded to metabolites which can be utilized in the intermediary metabolism. A similar, although more pronounced, distribution pattern and 14 CO 2 -exhalation (70% of i.v. dose) was observed after LA administration. The long time retention of heptane-soluble radioactivity in liver and fat (indicating unmetabolized substance) increased with degree of chlorination. On the contrary, the administration of LA and the chlorododecanes MCDD and PCDD I, but not of PCDD II, resulted in a selective labelling of the central nervous system 30-60 days after injection. (orig.)

  3. An evaluation of naturally occurring levels of polynuclear aromatic hydrocarbons in a small city and the impact on clean-up criteria and risk assessment - a case study

    Energy Technology Data Exchange (ETDEWEB)

    Cramer, C.A.; Lund, K.D. [Geraghty & Miller, Inc., Novi, MI (United States)

    1995-12-31

    Geraghty & Miller, Inc. conducted an investigation of potential manufactured gas plant (MGP) impacts at a site in a small city in the midwestern United States. Published literature pertaining to polynuclear aromatic hydrocarbon (PAH) levels in surface soils in urban environments has focused mainly on large historically urban areas. As a result, it has been difficult to correlate PAH levels encountered in surface soils during evaluations of MGP sites to typical urban background levels. An investigation completed by Geraghty & Miller of an MGP site in a city with a population of approximately 40 000 has shown that background levels of PAHs can range from non-detectable levels to as high as 44 milligrams/kilogram (mg/kg). The detailed surface-soil evaluation was necessary because a portion of the former MGP property is currently a residential apartment complex and is used as a playground for an elementary school. The regulatory agency required characterization of surface soils for MGP-indicator parameters such as PAHs, metals, cyanide, and volatile organics such as benzene, toluene, ethylbenzene, and xylenes (BTEX). Although the levels of total PAHs ranged as high as 31.5 mg/kg, Geraghty & Miller`s experience with similar sites suggested that the detected levels were likely indicative of urban background conditions. Many of the PAHs in urban soils are from recent activities not old industries. Before soil remediation current pollution sources should be checked.

  4. Inhibition of chlorine-induced pulmonary inflammation and edema by mometasone and budesonide

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Jing; Mo, Yiqun; Schlueter, Connie F.; Hoyle, Gary W., E-mail: Gary.Hoyle@louisville.edu

    2013-10-15

    Chlorine gas is a widely used industrial compound that is highly toxic by inhalation and is considered a chemical threat agent. Inhalation of high levels of chlorine results in acute lung injury characterized by pneumonitis, pulmonary edema, and decrements in lung function. Because inflammatory processes can promote damage in the injured lung, anti-inflammatory therapy may be of potential benefit for treating chemical-induced acute lung injury. We previously developed a chlorine inhalation model in which mice develop epithelial injury, neutrophilic inflammation, pulmonary edema, and impaired pulmonary function. This model was used to evaluate nine corticosteroids for the ability to inhibit chlorine-induced neutrophilic inflammation. Two of the most potent corticosteroids in this assay, mometasone and budesonide, were investigated further. Mometasone or budesonide administered intraperitoneally 1 h after chlorine inhalation caused a dose-dependent inhibition of neutrophil influx in lung tissue sections and in the number of neutrophils in lung lavage fluid. Budesonide, but not mometasone, reduced the levels of the neutrophil attractant CXCL1 in lavage fluid 6 h after exposure. Mometasone or budesonide also significantly inhibited pulmonary edema assessed 1 day after chlorine exposure. Chlorine inhalation resulted in airway hyperreactivity to inhaled methacholine, but neither mometasone nor budesonide significantly affected this parameter. The results suggest that mometasone and budesonide may represent potential treatments for chemical-induced lung injury. - Highlights: • Chlorine causes lung injury when inhaled and is considered a chemical threat agent. • Corticosteroids may inhibit lung injury through their anti-inflammatory actions. • Corticosteroids inhibited chlorine-induced pneumonitis and pulmonary edema. • Mometasone and budesonide are potential rescue treatments for chlorine lung injury.

  5. Two-phase ozonation of chlorinated organics

    International Nuclear Information System (INIS)

    Bhattacharyya, D.; Freshour, A.; West, D.

    1995-01-01

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

  6. Differentiation of naturally-occurring vs. artificial hydrocarbons in a landfill groundwater investigation

    International Nuclear Information System (INIS)

    Beaver, J.L.; Hartness, J.A.; Breeding, L.B.; Buchanan, D.M.

    1994-01-01

    Interpretation of groundwater sampling data at a large municipal/industrial landfill indicates contamination by both artificial and naturally-occurring hydrocarbons. Site hydrogeology consists of three different water bearing zones. The uppermost (shallow) aquifer is an unconfined unit consisting of silt, clay, and sand deposits. An intermediate depth semiconfined aquifer underlies the unconfined unit, and consists of a chert rubble zone and the upper portion of a fractured and solution-enhanced limestone formation. A regionally-extensive organic-rich shale underlies the semiconfined aquifer and separates it from the deep confined aquifer, which also consists of limestone. Groundwater investigations at the landfill have detected chlorinated and non-chlorinated hydrocarbons in the different aquifer intervals. Chlorinated hydrocarbons detected include tetrachloroethene, dichloroethene, and vinyl chloride and occur almost exclusively in the shallow aquifer. Aromatic hydrocarbons detected include benzene, toluene, ethylbenzene, and xylene (BTEX) and-occur in the intermediate and deep aquifers. The landfill was originally interpreted as the source of the contaminants. The observation of free-phase liquid hydrocarbons in the intermediate aquifer at the site, and high dissolved BTEX levels in the deep and intermediate aquifers upgradient of the landfill suggest that the aromatics were derived from a source other than the landfill. A potential source of BTEX contamination may be abandoned (pre-1930) natural gas wells located near the landfill. An additional BTEX source may be the organic-rich shale formation (a documented petroleum source rock)

  7. Study on removing chlorin by conversion-aborption of chlorin resin

    International Nuclear Information System (INIS)

    Huang Yunbai; Zhao Jinfang; Tang Zhijuan; Huang Qijin; Deng Jianguo

    2012-01-01

    Theon version of chlorin resin and the reclamation of acid and uranium in converting solution were investigated. The results indicated the residual chlorin can meet the requirement after converting, acid and uranium in converting solution can be reclaimed. (authors)

  8. Potassium chloride production by microcline chlorination

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-08-10

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

  9. Chlorine-36 investigations of salt lakes

    International Nuclear Information System (INIS)

    Chivas, A.R.; Kiss, E.

    1987-01-01

    The first chlorine-36 measurements are reported for surficial halite in lakes from a west-to-east traverse in Western Australia and from Lake Amadeus NT. Measurements of chlorine-36 were made using a 14 MV tandem accelerator. Isotopic chlorine ratios ranged from 8 to 53 x 10 exp-15, with no clear evidence for bomb-spike chlorine-36. The Western Australian samples have values close to secular equilibrium values for typical granite and groundwaters in this rock type. Studies are aimed at calculating the residence time of chloride in the surficial environment. 1 tab

  10. Chlorination of cooling water: a source of chlorine-containing organic compounds with possible environmental significance

    International Nuclear Information System (INIS)

    Jolley, R.L.; Gehrs, C.W.; Pitt, W.W. Jr.

    1976-01-01

    Chlorination of cooling waters may be a source of environmentally significant pollutants. Many water-soluble chlorine-containing organic compounds of low volatility were found in a sample of cooling water chlorinated to a 2-mg/l chlorine concentration in the laboratory. The compounds were separated and detected using a coupled 36 Cl-tracer--high-resolution liquid chromatographic technique developed at the Oak Ridge National Laboratory for determination of chlorinated organics in process effluents. For a chlorination contact time of 75 min at 25 0 C, the yield of chlorine in the form of chloro-organics amounted to 0.78% of the chlorine dosage. It is estimated that the yield is about 0.5% under typical reaction conditions in the electric power plant cooling system chosen for study. Because chlorine is commonly used to remove slime films from the cooling systems of electric power plants, as a means of maintaining high operational efficiency, it is estimated that several hundred tons of chlorinated organics are produced annually in the nation by this antifoulant process. The chromatographic elution positions of some of the separated constituents correspond to those of compounds separated and partially identified from chlorinated sewage treatment plant effluents. The results of this study indicate the formation of chloro-organics during the chlorination of cooling waters should be thoroughly examined, particularly with respect to their identification and determination of possible toxicological properties

  11. Data for comparison of chlorine dioxide and chlorine disinfection power in a real dairy wastewater effluent

    Directory of Open Access Journals (Sweden)

    Maliheh Akhlaghi

    2018-06-01

    Full Text Available Disinfection of water refers to a special operation that is doing to kill or disable causative organisms (i.e. Pathogens and in particular, intestinal bacteria. The aim of this pilot study is comparison of disinfection power of Chlorine dioxide and chlorine in a real dairy wastewater effluent. In this regard, firstly prepared two 220-l tanks made of polyethylene as reaction tanks and filled by effluent of a dairy wastewater treatment plant. Both tanks were equipped with mechanical stirrer. Then a Diaphragm dosing pumps with the maximum capacity of 3.9 l per hour were used for the chlorine dioxide and chlorine (Calcium hypochlorite 0.5 up to 3 ppm injection. Residual level of Chlorine dioxide and Chlorine were measured by portable photometric method DT4B kit, Germany. Finally, the Multiple-Tube Fermentation, Brilliant Green Bile Broth (BGB and Eosin methylene blue Agar (EMB technique was used for microbial analysis and the results were reported as the most probable number index (MPN respectively. The data showed that the residual of chlorine dioxide could stood more active than residual of chlorine in the aqueous environment significantly. Therefore, Use of chlorine dioxide is more effective than chlorine for removal fecal and total coliform from dairy wastewater effluent. Keywords: Disinfection, Chlorine dioxide, Chlorine, Total coliform, Fecal coliform

  12. DFT application for chlorin derivatives photosensitizer drugs modeling

    Science.gov (United States)

    Machado, Neila; Carvalho, B. G.; Téllez Soto, C. A.; Martin, A. A.; Favero, P. P.

    2018-04-01

    Photodynamic therapy is an alternative form of cancer treatment that meets the desire for a less aggressive approach to the body. It is based on the interaction between a photosensitizer, activating light, and molecular oxygen. This interaction results in a cascade of reactions that leads to localized cell death. Many studies have been conducted to discover an ideal photosensitizer, which aggregates all the desirable characteristics of a potent cell killer and generates minimal side effects. Using Density Functional Theory (DFT) implemented in the program Vienna Ab-initio Simulation Package, new chlorin derivatives with different functional groups were simulated to evaluate the different absorption wavelengths to permit resonant absorption with the incident laser. Gaussian 09 program was used to determine vibrational wave numbers and Natural Bond Orbitals. The chosen drug with the best characteristics for the photosensitizer was a modified model of the original chlorin, which was called as Thiol chlorin. According to our calculations it is stable and is 19.6% more efficient at optical absorption in 708 nm in comparison to the conventional chlorin e6. Vibrational modes, optical and electronic properties were predicted. In conclusion, this study is an attempt to improve the development of new photosensitizer drugs through computational methods that save time and contribute to decrease the numbers of animals for model application.

  13. Chlorinative stress in age-related diseases: a literature review.

    Science.gov (United States)

    Casciaro, Marco; Di Salvo, Eleonora; Pace, Elisabetta; Ventura-Spagnolo, Elvira; Navarra, Michele; Gangemi, Sebastiano

    2017-01-01

    Aging is an agglomerate of biological long-lasting processes that result being inevitable. Main actors in this scenario are both long-term inflammation and oxidative stress. It has been proved that oxidative stress induce alteration in proteins and this fact itself is critically important in the pathophysiological mechanisms leading to diseases typical of aging. Among reactive species, chlorine ones such as hypochlorous acid (HOCl) are cytotoxic oxidants produced by activated neutrophils during chronic inflammation processes. HOCl can also cause damages by reacting with biological molecules. HOCl is generated by myeloperoxidase (MPO) and augmented serum levels of MPO have been described in acute and chronic inflammatory conditions in cardiovascular patients and has been implicated in many inflammatory diseases such as atherosclerosis, neurodegenerative conditions, and some cancers. Due to these data, we decided to conduct an up-to-date review evaluating chlorinative stress effects on every age-related disease linked; potential anti-oxidant countermeasures were also assessed. Results obtained associated HOCl generation to the aging processes and confirmed its connection with diseases like neurodegenerative and cardiovascular pathologies, atherosclerosis and cancer; chlorination was mainly linked to diseases where molecular (protein) alteration constitute the major suspected cause: i.e. inflammation, tissue lesions, DNA damages, apoptosis and oxidative stress itself. According data collected, a healthy lifestyle together with some dietary suggestion and/or the administration of nutracetical antioxidant integrators could balance the effects of chlorinative stress and, in some cases, slow down or prevent the onset of age-releated diseases.

  14. Hydrocarbons and air pollution

    International Nuclear Information System (INIS)

    Herz, O.

    1992-01-01

    This paper shows the influence of hydrocarbons vapors, emitted by transports or by volatile solvents using, on air pollution. Hydrocarbons are the principal precursors of photochemical pollution. After a brief introduction on atmospheric chemistry and photochemical reactions, the author describes the french prevention program against hydrocarbons emissions. In the last chapter, informations on international or european community programs for photochemical pollution study are given. 5 figs., 10 tabs

  15. Production of hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Day, D T; Day, R E

    1920-04-27

    A process is disclosed of converting hydro-carbon oils having high boiling points to hydro-carbon oils having low boiling points, which process comprises adding the oil to be treated to a mass of hydro-carbon oil bearing shale, passing the shale with the oil through a conveyor retort and subjecting the material while in the retort to a heat treatment involving a temperature of at least 500/sup 0/F.

  16. Evaluation of genotoxic responses of Chaetoceros tenuissimus and Skeletonema costatum to water accommodated fraction of petroleum hydrocarbons as biomarker of exposure

    Digital Repository Service at National Institute of Oceanography (India)

    Desai, S.R.; Verlecar, X.N.; Ansari, Z.A.; Jagtap, T.G.; Sarkar, A.; Vashistha, D.; Dalal, S.G.

    by water accommodated fraction of petroleum hydrocarbons was assessed in terms of the DNA integrity measured by alkaline unwinding assay. The comparative study of the growth pattern of C. tenuissimus with respect to DNA integrity and the DNA strand breaks...

  17. Chlorination or monochloramination: Balancing the regulated trihalomethane formation and microbial inactivation in marine aquaculture waters

    KAUST Repository

    Sanawar, Huma

    2017-08-15

    Disinfection methods like chlorination are increasingly used to sanitize the water, equipment, tools and surfaces in aquaculture facilities. This is to improve water quality, and to maintain a hygienic environment for the well-being of aquatic organisms. However, chlorination can result in formation of regulated disinfection byproducts (DBPs) that can be carcinogenic and toxic. This study aims to evaluate if an optimal balance can be achieved between minimal regulated DBP formation and effective microbial inactivation with either chlorination or monochloramination for application in the Red Sea aquaculture waters. Upon chlorination, the concentration of total trihalomethanes (THMs), primarily bromoform, exceeded the regulatory limit of 80μg/L even at the lowest tested concentration of chlorine (1mg/L) and contact time (1h). Comparatively, regulated THMs concentration was only detectable at 30μg/L level in one of the three sets of monochloraminated marine aquaculture waters. The average log reduction of antibiotic-resistant bacteria (ARB) by chlorine ranged from 2.3-log to 3.2-log with different contact time. The average log reduction of ARB by monochloramine was comparatively lower at 1.9 to 2.9-log. Although viable Staphylococcus aureus was recovered from monochloraminated samples as opposed to chlorinated samples, the abundance of S. aureus was not high enough to result in any significant microbial risks. Both chlorination and monochloramination did not provide any significant improvement in the reduction of antibiotic resistance genes (ARGs). This study demonstrates that a systematic evaluation is needed to determine the optimal disinfectant required to balance both microbial and chemical risks. Compared to chlorine, monochloramine may be a more appropriate disinfection strategy for the treatment of aquaculture effluents prior to discharge or for recirculatory use in the aquaculture facility.

  18. Biomonitoring polycyclic aromatic hydrocarbons by Salix matsudana leaves: A comparison with the relevant air content and evaluation of environmental parameter effects

    Science.gov (United States)

    Zhao, Xiangai; He, Miao; Shang, Haibo; Yu, Hongling; Wang, Hao; Li, Huijie; Piao, Jingyi; Quinto, Maurizio; Li, Donghao

    2018-05-01

    Studies on seasonal distribution characteristics of polycyclic aromatic hydrocarbons (PAHs) in Salix matsudana leaves covering its annual life cycle were carried out in order to evaluate plant leaf response sensitivity to air pollution. Salix matsudana leaves were collected throughout different development phases of plant leaf inclusive of bud break to fallen leaves, covering from spring (May) to autumn (November). Simultaneously, particle and gas samples were collected using a high volume air sampler. Seven different PAHs were determined simultaneously in these samples. The temperature dependence of the partitioning of PAHs in air and plant leaves was investigated and the results were incorporated into a mathematical model. The measured plant/air partition coefficients have been found to be exponentially proportional to the reciprocal temperature, in agreement with theoretical expectations. Furthermore, in order to define the influence of different parameters on PAH adsorption on plant leaves, area and lipid leaf content were also measured. Results demonstrated that temperature plays a very important role in PAHs partitioning and that this value should be carefully considered during sampling, in order to obtain the best correlation between PAHs concentration in air and leaves.

  19. Effect of selection of pH in swimming pool on formation of chlorination by-products

    DEFF Research Database (Denmark)

    Hansen, Kamilla Marie Speht; Willach, Sarah; Mosbæk, Hans

    2011-01-01

    Chlorine is used as disinfection agent in public swimming pools, but also reacts with organic matter in the water forming chlorinat ed disinfection by-products. In order to evaluate the effect of choice of pHsetpoint in the pool we investigated the effect of chlorination of artificial body fluid...

  20. Manganese dioxide nanosheets as an optical probe for photometric determination of free chlorine

    International Nuclear Information System (INIS)

    Yu, Haili; Zheng, Lei

    2016-01-01

    We report on a colorimetric assay for free chlorine using MnO 2 nanosheets as an optical probe. In the absence of free chlorine, the addition of ascorbic acid (AA) causes the chemical dissolution of MnO 2 nanosheets via a redox reaction to result in low absorbance. However, if a solution containing free chlorine is added to the system, AA will be oxidized by free chlorine and the MnO 2 nanosheets will not longer be dissolved. Hence, the AA-induced decoloration will not take place and solution will remain yellow. Under optimized experimental conditions, there is a linear relationship between the change in absorbance at 370 nm and the concentration of free chlorine in the 0.2 to 10 μM concentration range, with an 80 nM detection limit. The detection limit for visual evaluation is 8.0 μM. The assay is fairly selective for free chlorine over common inorganic ions and small organic substances. It was applied to the determination of free chlorine in tap water using the standard addition method. (author)

  1. Chlorination of uranium oxides with CCl4 using a mechanochemical method

    Science.gov (United States)

    Kitawaki, Shinichi; Nagai, Takayuki; Sato, Nobuaki

    2013-08-01

    A chlorination method for uranium oxides at low temperature was investigated by using a mechanochemical method. In particular, the possibility of the chlorination of uranium oxides, such as UO2 and U3O8, via mechanochemical reaction with CCl4 was studied using a planetary ball mill. Mechanochemical experiments were conducted to evaluate the effect of milling time, CCl4/uranium oxide molar ratio, and revolution speed on the reaction. The synthesized products were then subjected to X-ray diffraction analysis, and it was found that the chlorination of U3O8 with CCl4 to UOCl2, UCl4, and U2O2Cl5 proceeded. However, the chlorination reaction could not be observed when using UO2 powder as the raw material. The chlorination reaction could not be observed when using UO2 powder as the raw material. The chlorination of U3O8 with CCl4 to form UOCl2, UCl4, and U2O2Cl5 via mechanochemical reaction occurs at room temperature. The ratio of chlorination increases with milling time when the appropriate amount of CCl4 is employed. However, the use of excess liquid CCl4 decreases the mechanochemical effect.

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

    NARCIS (Netherlands)

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

    1997-01-01

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

  3. Genotoxic effect of polycyclic aromatic hydrocarbons in the metropolitan area of Porto Alegre, Brazil, evaluated by Helix aspersa (Mueller, 1774)

    Energy Technology Data Exchange (ETDEWEB)

    Ianistcki, M. [Laboratorio de Genetica Toxicologica, Department of Biology, ULBRA, Av. Farroupilha 8001, Pr. 14/Sala 218, Bairro Sao Jose, CEP 92425-900 Canoas, RS (Brazil); Dallarosa, J. [Laboratorio de Ecologia, UFRGS (Brazil); Sauer, C.; Teixeira, C.E. [Fundacao Estadual de Protecao Ambiental Henrique Luis Roessler, FEPAM, RS (Brazil); Silva, J. da, E-mail: juliana.silva@ulbra.b [Laboratorio de Genetica Toxicologica, Department of Biology, ULBRA, Av. Farroupilha 8001, Pr. 14/Sala 218, Bairro Sao Jose, CEP 92425-900 Canoas, RS (Brazil)

    2009-07-15

    The purpose of this study was to biomonitor metropolitan areas of Porto Alegre (Brazil) for PAHs associated with atmospheric particles and check their effects on the DNA of the land mollusk Helix aspersa. The sampling sites are located in an urban area with heavy traffic: (i) Canoas, (ii) Sapucaia do Sul, and (iii) FIERGS/Porto Alegre. The samples were collected during a continuous period of 24 hours during 15 days using Stacked Filter Units (SFU) on polycarbonate filters (two separated size fractions: PM{sub 10-2.5} and PM{sub <2.5}). The concentrations of 16 major PAHs were determined according to EPA. Comet assay on H. aspersa hemolymph cells was chosen for genotoxicity evaluation. This evaluation shows that, in general, the smaller PM-size fractions (PM{sub <2.5}) have the highest genotoxicity and contain higher concentrations of extractable organic matter. In addition, associations between chemical characteristics and PM carcinogenicity tend to be stronger for the smaller PM-size fractions. - DNA damage in H. aspersa exposed to atmospheric particulate in Metropolitan Area of Porto Alegre demonstrated association with PAHs in the fine filter (PM{sub <2.5}).

  4. Chlorinated aliphatic and aromatic VOC decomposition in air mixture by using electron beam irradiation

    International Nuclear Information System (INIS)

    Chmielewski, A.G.; Sun Yongxia; Bulka, S.; Zimek, Z.

    2004-01-01

    Chlorinated aliphatic and aromatic hydrocarbons, which are emitted from coal power station and waste incinerators, are very harmful to the environment and human health. Recent studies show that chlorinated aliphatic and aromatic hydrocarbons are suspected to be the precursors of dioxin's formation. Dioxin's emission into atmosphere will cause severe environmental problems by ecology contamination. l,4-dichlorobenzene(l,4-DCB) and cis-dichloroethylene(cis-DCE) were chosen as representative chlorinated aromatic and aliphatic compounds, respectively. Their decomposition was investigated by electron beam irradiation. The experiments were carried out 'in batch' system. It is found that over 97% cis-DCE is decomposed having an initial concentration of 661 ppm. G-values of cis-DCE decomposition vary from 10 to 28 (molecules/100 eV) for initial concentration of 270-1530 ppm cis-DCE. The decomposition is mainly caused by secondary electron attachment and Cl addition reactions. Comparing with cis-DCE, 1,4-DCB decomposition needs higher absorbed dose. G-value of 1,4-DCB is below 4 molecules/100 eV

  5. Comprehensive Model for Enhanced Biodegradation of Chlorinated Solvents in Groundwater

    Science.gov (United States)

    Kouznetsova, I.; Gerhard, J. I.; Mao, X.; Robinson, C.; Barry, A. D.; Harkness, M.; Mack, E. E.; Dworatzek, S.

    2007-12-01

    SABRE (Source Area BioREmediation) is a public/private consortium whose charter is to de-termine if enhanced anaerobic bioremediation can result in effective treatment of chlorinated solvent DNAPL source areas. The focus of this 4-year, $5.7 million research and development project is a field site in the United Kingdom containing TCE DNAPL. A comprehensive numerical model for simulating dehalogenation of chlorinated ethenes has been developed. The model considers the kinetic dissolution of DNAPL and nonaqueous organic amendments, bacterial growth and decay, and the interaction of biological and geochemical reactions that might influence biological activity. The model accounts for inhibitory effects of high chlorin-ated solvent concentrations as well as the link between fermentation and dehalogenation due to dynamic hydrogen concentration (the direct electron donor). In addition to the standard biodegradation pathways, sulphate reduction, mineral dissolution and precipitation kinetics are incorporated. These latter processes influence the soil buffering capacity and thus the net acidity generated. One-dimensional simulations were carried out to reproduce the data from columns packed with site soil and groundwater exhibiting both intermediate (250 mg/L) and near solubility (1100 mg/L) TCE concentrations. The modelling aims were to evaluate the key processes underpinning bioremediation success and provide a tool for investigating field sys-tem sensitivity to site data and design variables. This paper will present the model basis and validation and examine sensitivity to key processes including chlorinated ethene partitioning into soybean oil, sulphate reduction, and geochemical influences such as pH and the role of buffering in highly dechlorinating systems.

  6. Plasma devices for hydrocarbon reformation

    KAUST Repository

    Cha, Min

    2017-01-01

    Plasma devices for hydrocarbon reformation are provided. Methods of using the devices for hydrocarbon reformation are also provided. The devices can include a liquid container to receive a hydrocarbon source, and a plasma torch configured

  7. Chlorine demand and residual chlorine decay kinetics of Kali river water at Kaiga project area

    International Nuclear Information System (INIS)

    Krishna Bhat, D.; Prakash, T.R.; Thimme Gowda, B.; Sherigara, B.S.; Khader, A.M.A.

    1995-01-01

    The nuclear power plant at Kaiga would use Kali river water for condenser cooling. This necessitated studies on the chemistry of chlorination such as chlorine demand, kinetics of chlorination and other water characteristics aimed at obtaining base line data. The study revealed significant seasonal variation of chlorine demand ranging from 0.5 ppm to 1.7 ppm (3.0 ppm dose, 30 min contact time) and total consumption of 5.0 ppm (10.0 ppm dose, 48 hours contact time). The reaction follows first order kinetics in chlorine. High correlation of chlorine demand with chlorophyll a, suspended matter, turbidity, silica, nitrite, phosphate and sulphate indicated that chlorine demand is greatly influenced by water quality. (author). 3 refs., 1 tab

  8. Monitoring chlorination practices during operation at TAPS

    International Nuclear Information System (INIS)

    Sriraman, A.K.; Wani, B.N.; Gokhale, A.S.; Yuvaraju, B.

    1995-01-01

    Chlorination of cooling waters is aimed at the condenser surfaces to minimize the biogrowth, while the residual oxidants in the effluents are negligible. This paper describes the fulfillment of the above criteria, as observed during the monitoring of chlorination practices at Tarapur Atomic Power Station (TAPS) during 1990. (author). 4 refs., 2 tabs

  9. Elements from chlorine to calcium nuclear reactions

    CERN Document Server

    Kunz, Wunibald

    1968-01-01

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

  10. The Synthesis of Carbon Nanomaterials using Chlorinated ...

    African Journals Online (AJOL)

    The effect of chlorine on the morphology of carbon nanotubes (CNTs) prepared from a Fe-Co/CaCO3 catalyst was investigated using chlorobenzene (CB), dichlorobenzene (DCB), trichlorobenzene (TCB), dichloroethane (DCE), trichloroethane (TCE) and tetrachloroethane (TTCE) as chlorine sources using a catalytic ...

  11. A new chlorine logging tool: Application in the oilfield development with high salinity formation water

    International Nuclear Information System (INIS)

    Qing-Yuan, He; Xin-Miao, Hu; Geng-Fei, Wu; Wen-DA, J.

    1997-01-01

    Radiating formations with isotopes neutron source (Am-Be), and using chlorine element contained in the formation water as a tracer indicator, the chlorine spectrum well logging tool has been regarded as the important and useful tool in the determination of water flooding intensity of formation intervals, especially in the oilfield development stages with high salinity formation water. However, the accuracy of determination of the oil/water-bearings needs to be improved. A new chlorine spectrum logging tool with two detectors has been developed. The short (near) detector uses a He-3 counter tube to measure formation epithermal neutron intensity, the long (far) detector uses a BGO crystal detector to replace traditional Nal detector for measuring the captured X gamma ray spectrum produced by the thermal neutron capture process in the formation. Although the energy resolution of BGO detector to gamma rays is less effective than that of Nal detector, the efficiency of BGO detector to high energy gamma rays is much better. This advantage helps to detect captured chlorine gamma rays, which increases the ability of chlorine element detection. The effect of statistical errors is also reduced. The spectrum autostabilization function in the downhole tool improves the reliability of the whole system. The new chlorine spectrum logging tool can give three log curves simultaneously, these curves are formation porosity, chlorine content, and the ratio of chlorine content and thermal neutron intensity. When formation porosity is larger than 10 p.u, formation water salinity is greater than 40,000 ppm, the resolution to the oil/water-bearings is increased to about 10% compared with the old version tool. Field tests show that the accuracy of water flooding intensity evaluation has been upgraded considerably with the use of new chlorine spectrum logging tool, which contributes greatly to the oilfield development with high salinity formation water

  12. A new chlorine logging tool: Application in the oilfield development with high salinity formation water

    Energy Technology Data Exchange (ETDEWEB)

    Qing-Yuan, He; Xin-Miao, Hu; Geng-Fei, Wu [China National Petroleum Corp. (China). Jianghan Well Logging Institute; Wen-DA, J. [China National Petroleum Corp. (China). Development Bureau

    1997-10-01

    Radiating formations with isotopes neutron source (Am-Be), and using chlorine element contained in the formation water as a tracer indicator, the chlorine spectrum well logging tool has been regarded as the important and useful tool in the determination of water flooding intensity of formation intervals, especially in the oilfield development stages with high salinity formation water. However, the accuracy of determination of the oil/water-bearings needs to be improved. A new chlorine spectrum logging tool with two detectors has been developed. The short (near) detector uses a He-3 counter tube to measure formation epithermal neutron intensity, the long (far) detector uses a BGO crystal detector to replace traditional Nal detector for measuring the captured X gamma ray spectrum produced by the thermal neutron capture process in the formation. Although the energy resolution of BGO detector to gamma rays is less effective than that of Nal detector, the efficiency of BGO detector to high energy gamma rays is much better. This advantage helps to detect captured chlorine gamma rays, which increases the ability of chlorine element detection. The effect of statistical errors is also reduced. The spectrum autostabilization function in the downhole tool improves the reliability of the whole system. The new chlorine spectrum logging tool can give three log curves simultaneously, these curves are formation porosity, chlorine content, and the ratio of chlorine content and thermal neutron intensity. When formation porosity is larger than 10 p.u, formation water salinity is greater than 40,000 ppm, the resolution to the oil/water-bearings is increased to about 10% compared with the old version tool. Field tests show that the accuracy of water flooding intensity evaluation has been upgraded considerably with the use of new chlorine spectrum logging tool, which contributes greatly to the oilfield development with high salinity formation water 4 refs., 2 tabs., 7 figs.

  13. Internal chlorination of Ni-Cr alloys

    Energy Technology Data Exchange (ETDEWEB)

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

    1998-12-31

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

  14. Minimization of zirconium chlorinator residues

    International Nuclear Information System (INIS)

    Green, G.K.; Harbuck, D.D.

    1995-01-01

    Zirconium chlorinator residues contain an array of rare earths, scandium, unreacted coke, and radioactive thorium and radium. Because of the radioactivity, the residues must be disposed in special waste containment facilities. As these sites become more congested, and with stricter environmental regulations, disposal of large volumes of wastes may become more difficult. To reduce the mass of disposed material, the US Bureau of Mines (USBM) developed technology to recover rare earths, thorium and radium, and unreacted coke from these residues. This technology employs an HCl leach to solubilize over 99% of the scandium and thorium, and over 90% of the rare earths. The leach liquor is processed through several solvent extraction stages to selectively recover scandium, thorium, and rare earths. The leach residue is further leached with an organic acid to solubilize radium, thus allowing unreacted coke to be recycled to the chlorinator. The thorium and radium waste products, which comprise only 2.1% of the original residue mass, can then be sent to the radioactive waste facility

  15. Radiochemical analysis of chlorine-36

    International Nuclear Information System (INIS)

    Rodriguez, M.; Pina, G.; Lara, E.

    2006-01-01

    The radioactive chlorine isotope, 36 Cl, decays with a half-life of 3x10 5 years by emitting a beta particle (98 %) and by electron capture. The aim of this paper is to propose a radiochemical separation method of 36 Cl 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 36 Cl inventory calculations. The separation method proposed is based on an oxidation technique where chlorine is trapped by NaOH. 36 Cl beta emissions are measured by liquid scintillation counting by the dual label technique in order to avoid the contamination produced by 14 C 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. (author)

  16. Determination of the total amount of organically bound chlorine, bromine and iodine in environmental samples by instrumental neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    Gether, J; Lunde, G [Central Institute for Industrial Research, Oslo (Norway); Steinnes, E [Institutt for Atomenergi, Kjeller (Norway)

    1979-07-01

    The determination of chlorine, bromine and iodine present as non-polar, hydrophobic hydrocarbons in environmental samples is reported. The organohalogen compounds are seprated from water into an organic phase by on-site liquid-liquid extraction, and form biological material by procedures based on lipid phase extraction and codistillation. After removal of inorganic halides by washing with water and concentration of the sample by evaporation of the solvent, the resulting extracts are analyzed for their chlorine, bromine and iodine contents by instrumental neutron activation analysus. Strict attention is paid to the possibility of contamination in every step of the procedure. Background values in routine analysis are approximately 100-200 ng of chlorine, <5 ng of bromine and <3 ng of iodine.

  17. Highly Efficient and Reproducible Nonfullerene Solar Cells from Hydrocarbon Solvents

    KAUST Repository

    Wadsworth, Andrew; Ashraf, Raja; Abdelsamie, Maged; Pont, Sebastian; Little, Mark; Moser, Maximilian; Hamid, Zeinab; Neophytou, Marios; Zhang, Weimin; Amassian, Aram; Durrant, James R.; Baran, Derya; McCulloch, Iain

    2017-01-01

    With chlorinated solvents unlikely to be permitted for use in solution-processed organic solar cells in industry, there must be a focus on developing nonchlorinated solvent systems. Here we report high-efficiency devices utilizing a low-bandgap donor polymer (PffBT4T-2DT) and a nonfullerene acceptor (EH-IDTBR) from hydrocarbon solvents and without using additives. When mesitylene was used as the solvent, rather than chlorobenzene, an improved power conversion efficiency (11.1%) was achieved without the need for pre- or post-treatments. Despite altering the processing conditions to environmentally friendly solvents and room-temperature coating, grazing incident X-ray measurements confirmed that active layers processed from hydrocarbon solvents retained the robust nanomorphology obtained with hot-processed chlorinated solvents. The main advantages of hydrocarbon solvent-processed devices, besides the improved efficiencies, were the reproducibility and storage lifetime of devices. Mesitylene devices showed better reproducibility and shelf life up to 4000 h with PCE dropping by only 8% of its initial value.

  18. Highly Efficient and Reproducible Nonfullerene Solar Cells from Hydrocarbon Solvents

    KAUST Repository

    Wadsworth, Andrew

    2017-06-01

    With chlorinated solvents unlikely to be permitted for use in solution-processed organic solar cells in industry, there must be a focus on developing nonchlorinated solvent systems. Here we report high-efficiency devices utilizing a low-bandgap donor polymer (PffBT4T-2DT) and a nonfullerene acceptor (EH-IDTBR) from hydrocarbon solvents and without using additives. When mesitylene was used as the solvent, rather than chlorobenzene, an improved power conversion efficiency (11.1%) was achieved without the need for pre- or post-treatments. Despite altering the processing conditions to environmentally friendly solvents and room-temperature coating, grazing incident X-ray measurements confirmed that active layers processed from hydrocarbon solvents retained the robust nanomorphology obtained with hot-processed chlorinated solvents. The main advantages of hydrocarbon solvent-processed devices, besides the improved efficiencies, were the reproducibility and storage lifetime of devices. Mesitylene devices showed better reproducibility and shelf life up to 4000 h with PCE dropping by only 8% of its initial value.

  19. Plasma devices for hydrocarbon reformation

    KAUST Repository

    Cha, Min Suk

    2017-02-16

    Plasma devices for hydrocarbon reformation are provided. Methods of using the devices for hydrocarbon reformation are also provided. The devices can include a liquid container to receive a hydrocarbon source, and a plasma torch configured to be submerged in the liquid. The plasma plume from the plasma torch can cause reformation of the hydrocarbon. The device can use a variety of plasma torches that can be arranged in a variety of positions in the liquid container. The devices can be used for the reformation of gaseous hydrocarbons and/or liquid hydrocarbons. The reformation can produce methane, lower hydrocarbons, higher hydrocarbons, hydrogen gas, water, carbon dioxide, carbon monoxide, or a combination thereof.

  20. Chlorination of irradiated polyethylene single crystals

    International Nuclear Information System (INIS)

    Grimm, H.J.

    1978-01-01

    The chlorination of electron beam-irradiation polyethylene (PE) single crystals was studied for a range of irradiation doses, temperatures, and chlorine interaction times. The results presented show that PE chlorination was quite extensive, even in unirradiated PE single crystals at 25 0 C in the dark. Electron Spin Resonance (ESR, EPR) was used in this study in order to determine the alkyl radical concentration, decay constant, and diffusivity for (unchlorinated) specimens. An alkyl radical diffusivity D/sub a/ = 1.6 x 10 -17 cm 2 /sec at 25 0 C was estimated from ESR data and alkyl radical migration as one-dimensional unsteady-state diffusion process. In irradiated PE, chlorination occurred mainly via chain reactions which were initiated by the irradiation-produced free radicals. Chlorine content values were determined by X-ray Energy Spectroscopy (XES). It was found that the magnitude of the chlorine uptake increased with increasing dose, and decreased with decreasing temperature at constant dose. Otherwise the observed PE chlorination phenomena was quite similar for all of the doses and temperatures studied here, consisting of a two step mechanism: a fast uptake which occurred between time tCl 2 = 0 - 5 minutes and a slower, approximately first-order rate of uptake which occurred between times tCl 2 = 5 - 120 minutes. Chlorination was essentially complete by time tCl 2 = 120 minutes. The rapid uptake probably occurred in the amorphous surface zones where Cl 2 is relatively high and the second, slower step was probably attributable to Cl 2 diffusion into the crystalline regions and subsequent chlorination there. Inasmuch as the PE density decreases with increasing dose (for 1-600 Mrad), Cl 2 diffusivity was enhanced, resulting in higher chlorine uptake values at higher doses

  1. Selection and Evaluation of Alternative Solvents for Caprolactam Extraction

    NARCIS (Netherlands)

    van Delden, M.L.; Kuipers, N.J.M.; de Haan, A.B.

    2006-01-01

    Because of the strict legislation for currently applied solvents in the industrial extraction of caprolactam, being benzene, toluene and chlorinated hydrocarbons, a need exists for alternative, environmentally benign solvents. An experimental screening procedure consisting of several steps was used

  2. Selection and evaluation of alternative solvents for caprolactam extraction

    NARCIS (Netherlands)

    Delden, van M.L.; Kuipers, N.J.M.; Haan, de A.B.

    2006-01-01

    Because of the strict legislation for currently applied solvents in the industrial extraction of caprolactam, being benzene, toluene and chlorinated hydrocarbons, a need exists for alternative, environmentally benign solvents. An experimental screening procedure consisting of several steps was used

  3. Direct Push Optical Screening Tool for High Resolution, Real-Time Mapping of Chlorinated Solvent DNAPL Architecture

    Science.gov (United States)

    2016-07-01

    petroleum hydrocarbon fuels due to higher densities, lower viscosities , and increased weathering (mass depletion) of residual chlorinated solvent DNAPL...generally classified as stratified layers of fine sand and silt with few clay layers. A silt layer was penetrated consistently at a depth of about 45...e.g., stiff clays ) there is potential for the thickness of the dye interaction zone to increase to approximately 1-2 mm. Intuition suggests that this

  4. Discriminative stimulus effects of inhaled 1,1,1-trichloroethane in mice: comparison to other hydrocarbon vapors and volatile anesthetics.

    Science.gov (United States)

    Shelton, Keith L

    2009-04-01

    Because the toxicity of many inhalants precludes evaluation in humans, drug discrimination, an animal model of subjective effects, can be used to gain insights on their poorly understood abuse-related effects. The purpose of the present study was to train a prototypic inhalant that has known abuse liability, 1,1,1-trichloroethane (TCE), as a discriminative stimulus in mice, and compare it to other classes of inhalants. Eight B6SJLF1/J mice were trained to discriminate 10 min of exposure to 12,000 ppm inhaled TCE vapor from air and seven mice were trained to discriminate 4,000 ppm TCE from air. Tests were then conducted to characterize the discriminative stimulus of TCE and to compare it to representative aromatic and chlorinated hydrocarbon vapors, volatile halogenated anesthetics as well as an odorant compound. Only the 12,000 ppm TCE versus the air discrimination group exhibited sufficient discrimination accuracy for substitution testing. TCE vapor concentration- and exposure time-dependently substituted for the 12,000 ppm TCE vapor training stimulus. Full substitution was produced by trichloroethylene, toluene, enflurane, and sevoflurane. Varying degrees of partial substitution were produced by the other volatile test compounds. The odorant, 2-butanol, did not produce any substitution for TCE. The discriminative stimulus effects of TCE are shared fully or partially by chlorinated and aromatic hydrocarbons as well as by halogenated volatile anesthetics. However, these compounds can be differentiated from TCE both quantitatively and qualitatively. It appears that the degree of similarity is not solely a function of chemical classification but may also be dependent upon the neurochemical effects of the individual compounds.

  5. Decontamination of Pangasius fish (Pangasius hypophthalmus) with chlorine or peracetic acid in the laboratory and in a Vietnamese processing company.

    Science.gov (United States)

    Tong Thi, Anh Ngoc; Sampers, Imca; Van Haute, Sam; Samapundo, Simbarashe; Ly Nguyen, Binh; Heyndrickx, Marc; Devlieghere, Frank

    2015-09-02

    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. Copyright © 2015. Published by Elsevier B.V.

  6. Quantifying Short-Chain Chlorinated Paraffin Congener Groups

    NARCIS (Netherlands)

    Yuan, Bo; Bogdal, Christian; Berger, Urs; MacLeod, Matthew; Gebbink, Wouter A.; Alsberg, Tomas; Wit, de Cynthia A.

    2017-01-01

    Accurate quantification of short-chain chlorinated paraffins (SCCPs) poses an exceptional challenge to analytical chemists. SCCPs are complex mixtures of chlorinated alkanes with variable chain length and chlorination level; congeners with a fixed chain length (n) and number of chlorines (m) are

  7. Aryl hydrocarbon receptor (AhR) inducers and estrogen receptor (ER) activities in surface sediments of Three Gorges Reservoir, China evaluated with in vitro cell bioassays

    NARCIS (Netherlands)

    Wang, J.; Bovee, T.F.H.; Bi, Y.; Bernhöft, S.; Schramm, K.W.

    2014-01-01

    Two types of biological tests were employed for monitoring the toxicological profile of sediment cores in the Three Gorges Reservoir (TGR), China. In the present study, sediments collected in June 2010 from TGR were analyzed for estrogen receptor (ER)- and aryl hydrocarbon receptor (AhR)-mediated

  8. Thraustochytrid protists degrade hydrocarbons

    Digital Repository Service at National Institute of Oceanography (India)

    Raikar, M.T.; Raghukumar, S.; Vani, V.; David, J.J.; Chandramohan, D.

    isolation tubes with crude oil. Three isolates tested showed positive hydrophobicity of cell walls as judged by the Microbial Adhesion to Hydrocarbons (MATH) assay. Addition of Bombay High crude oil to nutrient broth slightly enhanced growth of the protists...

  9. Chlorine isn't Just for Swimming Pools Anymore... Chlorination of Organic Compounds in the Arctic

    Science.gov (United States)

    Han, A.; Raab, T. K.

    2013-12-01

    The cycling of chlorine between its organic and inorganic forms is known to occur in forest soils, but little is known about the generality of this mechanism, which soil components chlorine attaches to, and at what rate chlorination occurs. The study uses peat-rich tundra soils from Barrow, Alaska varying in age since formation of 50 yrs - 5500 yrs BP, and seeks to measure the rate at which organic molecules are chlorinated and to understand what changes those molecules undergo once chlorinated. Soil abundance of chlorine and bromine was estimated in soils of varying age using X-ray fluorescence, and org-Cl levels were measured using pyro-hydrolysis [Table 1]. We considered activity of the enzyme Chloroperoxidase, and data was gathered using absorbance scans of the organic molecule monochlorodimedone to determine whether it had been chlorinated and if so, at what rate. Additional information was gathered from the chlorination of small organic components of the macromolecule lignin, whose constituent molecules make up a large portion of humic materials critical to soil health, through emission scans and fluorescence scans. The results showed that the enzyme chloroperoxidase, which is found in nature and is associated with fungi or bacteria, attaches a chlorine atom to monochlorodimedone and that similar enzymes found in Arctic soils act on it, as well as the lignin model subunits cinnamaldehyde ((2E)-3-phenylprop-2-enal) and naringenin-7-rhamnoglucoside. The results may provide more information on chlorination rates in the Arctic and may contribute to an understanding of how and at what rate chlorine changes form in nature, and answer questions about ozone deterioration or anthropogenic chlorine impact(s) on the environment.Average Halogen Abundance in Arctic Soils xrf=Energy Dispersive X-Ray Fluorescencepyro= TOX Pyro-Hydrolysis

  10. Purifying hydrocarbon oils

    Energy Technology Data Exchange (ETDEWEB)

    Rostin, H

    1938-08-11

    A process is described for continuously purifying hydrocarbon oils consisting in conducting the vapors of the same at a temperature of 300 to 400/sup 0/C over the oelitic ore minette together with reducing gases in presence of steam the proportion of the reducing gases and steam being such that the sulfur of the hydrocarbons escapes from the reaction chamber in the form of sulfuretted hydrogen without permanent sulfide of iron being formed.

  11. Process for refining hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Risenfeld, E H

    1924-11-26

    A process is disclosed for the refining of hydrocarbons or other mixtures through treatment in vapor form with metal catalysts, characterized by such metals being used as catalysts, which are obtained by reduction of the oxide of minerals containing the iron group, and by the vapors of the hydrocarbons, in the presence of the water vapor, being led over these catalysts at temperatures from 200 to 300/sup 0/C.

  12. Determination of chlorine in nuclear-grade uranium compounds

    International Nuclear Information System (INIS)

    Yang Chunqing; Liu Fuyun; Huang Dianfan

    1988-01-01

    The determination of chlorine in nuclear-grade uranium compounds is discribed. Chlorine is separated from uranium oxide pyrohydrolytically with stream of wet oxygen in a furnace at 800 ∼ 900 deg C. Chlorine is volatilized as hydrochloric acid, absorbed in a dilute alkaline solution and measured with chlorine-selective electrode. This method covers the concentration range of 10 ∼ 500 pm chlorine in uranium oxide. Precision of at least ± 10% and recovery of 85 ∼ 108% have been reported

  13. Biodegradation of petroleum hydrocarbons at low temperatures

    International Nuclear Information System (INIS)

    Whyte, L. G.; Greer, C W.

    1999-01-01

    Bioremediation of contaminated Arctic sites has been proposed as the logistically and economically most favorable solution despite the known technical difficulties. The difficulties involve the inhibition of pollutants removal by biodegradation below freezing temperatures and the relative slowness of the process to remove enough hydrocarbon pollutants during the above-freezing summer months. Despite these formidable drawbacks, biodegradation of hydrocarbon contaminants is possible even in below-zero temperatures, especially if indigenous psychrophilic and psychrotropic micro-organism are used. This paper reports results of a study involving several hydrocarbon-degrading psychrotropic bacteria and suggests bioaugmentation with specific cold-adapted organisms and/or biostimulation with commercial fertilizers for enhancing degradation of specific contaminants in soils from northern Canada. An evaluation of the biodegradation potential of hydrocarbon contaminated soils in the high Arctic suggested that the contaminated soils contained sufficient numbers of cold-adapted hydrocarbon-degrading bacteria and that the addition of fertilizer was sufficient to enhance the level of hydrocarbon degradation at low ambient summer temperatures. 9 refs., 2 tabs., 3 figs

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

    Science.gov (United States)

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

    2014-05-01

    Disinfection is the last treatment stage of a Drinking Water Treatment Plant (DWTP) and is carried out to maintain a residual concentration of disinfectant in the water distribution system. Chlorine dioxide (ClO2) is a widely used chemical employed for this purpose. The aim of this work was to evaluate the influence of several treatments on chlorine dioxide consumption and on chlorite and chlorate formation in the final oxidation/disinfection stage. A number of tests was performed at laboratory scale employing water samples collected from the DWTP of Cremona (Italy). The following processes were studied: oxidation with potassium permanganate, chlorine dioxide and sodium hypochlorite, coagulation/flocculation with ferric chloride and aluminum sulfate, filtration and adsorption onto activated carbon. The results showed that the chlorine dioxide demand is high if sodium hypochlorite or potassium permanganate are employed in pre-oxidation. On the other hand, chlorine dioxide leads to the highest production of chlorite and chlorate. The coagulation/flocculation process after pre-oxidation shows that chlorine dioxide demand decreases if potassium permanganate is employed as an oxidant, both with ferric chloride and aluminum sulfate. Therefore, the combination of these processes leads to a lower production of chlorite and chlorate. Aluminum sulfate is preferable in terms of the chlorine dioxide demand reduction and minimization of the chlorite and chlorate formation. Activated carbon is the most effective solution as it reduced the chlorine dioxide consumption by about 50% and the DBP formation by about 20-40%. Copyright © 2014 Elsevier Ltd. All rights reserved.

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

    Directory of Open Access Journals (Sweden)

    2007-04-01

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

  16. Recovery of actinides from actinide-aluminium alloys by chlorination: Part I

    Energy Technology Data Exchange (ETDEWEB)

    Cassayre, L., E-mail: cassayre@chimie.ups-tlse.fr [Laboratoire de Genie Chimique (LGC), Departement Procedes Electrochimiques, CNRS-UMR 5503, Universite de Toulouse III - Paul Sabatier, 31062 Toulouse (France); Soucek, P.; Mendes, E.; Malmbeck, R.; Nourry, C.; Eloirdi, R.; Glatz, J.-P. [European Commission, JRC, Institute for Transuranium Elements, Postfach 2340, 76125 Karlsruhe (Germany)

    2011-07-01

    Pyrochemical processes in molten LiCl-KCl are being developed in ITU for recovery of actinides from spent nuclear fuel. The fuel is anodically dissolved to the molten salt electrolyte and actinides are electrochemically reduced on solid aluminium cathodes forming solid actinide-aluminium alloys. A chlorination route is being investigated for recovery of actinides from the alloys. This route consists in three steps: Vacuum distillation for removal of the salt adhered on the electrode, chlorination of the actinide-aluminium alloys by chlorine gas and sublimation of the formed AlCl{sub 3}. A thermochemical study showed thermodynamic feasibility of all three steps. On the basis of the conditions identified by the calculations, experiments using pure UAl{sub 3} alloy were carried out to evaluate and optimise the chlorination step. The work was focused on determination of the optimal temperature and Cl{sub 2}/UAl{sub 3} molar ratio, providing complete chlorination of the alloy without formation of volatile UCl{sub 5} and UCl{sub 6}. The results showed high efficient chlorination at a temperature of 150 deg. C.

  17. Chlorination of uranium oxides with CCl4 using a mechanochemical method

    International Nuclear Information System (INIS)

    Kitawaki, Shinichi; Nagai, Takayuki; Sato, Nobuaki

    2013-01-01

    Highlights: • UCl 4 or UOCl 2 could be synthesized from U 3 O 8 with CCl 4 by using a planetary ball mill. • The chlorination could not be observed when using UO 2 powder as the starting material. • Extension of milling time was effective for chlorinating U 3 O 8 with the appropriate amount of CCl 4 . -- Abstract: A chlorination method for uranium oxides at low temperature was investigated by using a mechanochemical method. In particular, the possibility of the chlorination of uranium oxides, such as UO 2 and U 3 O 8 , via mechanochemical reaction with CCl 4 was studied using a planetary ball mill. Mechanochemical experiments were conducted to evaluate the effect of milling time, CCl 4 /uranium oxide molar ratio, and revolution speed on the reaction. The synthesized products were then subjected to X-ray diffraction analysis, and it was found that the chlorination of U 3 O 8 with CCl 4 to UOCl 2 , UCl 4 , and U 2 O 2 Cl 5 proceeded. However, the chlorination reaction could not be observed when using UO 2 powder as the raw material

  18. Chlorination of uranium oxides with CCl{sub 4} using a mechanochemical method

    Energy Technology Data Exchange (ETDEWEB)

    Kitawaki, Shinichi, E-mail: kitawaki.shinichi@jaea.go.jp [Nuclear Fuel Cycle Engineering Laboratories, Japan Atomic Energy Agency, 4-33 Muramatsu, Tokai, Naka, Ibaraki 319-1194 (Japan); Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, 2-1-1 Katahira, Aoba, Sendai, Miyagi 980-8577 (Japan); Nagai, Takayuki [Nuclear Fuel Cycle Engineering Laboratories, Japan Atomic Energy Agency, 4-33 Muramatsu, Tokai, Naka, Ibaraki 319-1194 (Japan); Sato, Nobuaki [Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, 2-1-1 Katahira, Aoba, Sendai, Miyagi 980-8577 (Japan)

    2013-08-15

    Highlights: • UCl{sub 4} or UOCl{sub 2} could be synthesized from U{sub 3}O{sub 8} with CCl{sub 4} by using a planetary ball mill. • The chlorination could not be observed when using UO{sub 2} powder as the starting material. • Extension of milling time was effective for chlorinating U{sub 3}O{sub 8} with the appropriate amount of CCl{sub 4}. -- Abstract: A chlorination method for uranium oxides at low temperature was investigated by using a mechanochemical method. In particular, the possibility of the chlorination of uranium oxides, such as UO{sub 2} and U{sub 3}O{sub 8}, via mechanochemical reaction with CCl{sub 4} was studied using a planetary ball mill. Mechanochemical experiments were conducted to evaluate the effect of milling time, CCl{sub 4}/uranium oxide molar ratio, and revolution speed on the reaction. The synthesized products were then subjected to X-ray diffraction analysis, and it was found that the chlorination of U{sub 3}O{sub 8} with CCl{sub 4} to UOCl{sub 2}, UCl{sub 4}, and U{sub 2}O{sub 2}Cl{sub 5} proceeded. However, the chlorination reaction could not be observed when using UO{sub 2} powder as the raw material.

  19. Recovery of actinides from actinide-aluminium alloys by chlorination: Part I

    International Nuclear Information System (INIS)

    Cassayre, L.; Soucek, P.; Mendes, E.; Malmbeck, R.; Nourry, C.; Eloirdi, R.; Glatz, J.-P.

    2011-01-01

    Pyrochemical processes in molten LiCl-KCl are being developed in ITU for recovery of actinides from spent nuclear fuel. The fuel is anodically dissolved to the molten salt electrolyte and actinides are electrochemically reduced on solid aluminium cathodes forming solid actinide-aluminium alloys. A chlorination route is being investigated for recovery of actinides from the alloys. This route consists in three steps: Vacuum distillation for removal of the salt adhered on the electrode, chlorination of the actinide-aluminium alloys by chlorine gas and sublimation of the formed AlCl 3 . A thermochemical study showed thermodynamic feasibility of all three steps. On the basis of the conditions identified by the calculations, experiments using pure UAl 3 alloy were carried out to evaluate and optimise the chlorination step. The work was focused on determination of the optimal temperature and Cl 2 /UAl 3 molar ratio, providing complete chlorination of the alloy without formation of volatile UCl 5 and UCl 6 . The results showed high efficient chlorination at a temperature of 150 deg. C.

  20. Thermochemical emission and transformation of chlorinated paraffins in inert and oxidizing atmospheres.

    Science.gov (United States)

    Xin, Shanzhi; Gao, Wei; Wang, Yawei; Jiang, Guibin

    2017-10-01

    Chlorinated paraffins (CPs) generally function as flame retardants and plasticizers in various materials. They are most likely to be processed by thermal processes during the entire life cycle. However, data on the formation and emission of CPs during thermal processes are still not fully understood. In this study, we simulated industrial thermal processes to investigate the emission of medium-chain chlorinated paraffins (MCCPs) and short-chain chlorinated paraffins (SCCPs) using commercial CP52 as the feedstock. We found that CP52 decomposed very easily at 210-320 °C. The decomposition of CPs generated large quantities of MCCPs and SCCPs. These remained in the residue at low temperature (∼200 °C) and were gradually released into the gas phase at higher temperatures. MCCPs and SCCPs were not detected in either the residue or the gas phase when the temperature exceeded 400 °C. However, considerable concentrations of aromatic and chlorinated aromatic hydrocarbons (Cl-PAHs) were identified in the gas phase, and they were formed as the amount of SCCPs and MCCPs decreased. Cl-PAHs were dominated by low-chlorinated chlorobenzenes, polychlorinated biphenyls, and polychlorinated naphthalenes. Oxygen promoted the release and decomposition of SCCPs in the gas phase. The results of the present study revealed the release of MCCPs and SCCPs and their synergistic emission with Cl-PAHs when CPs were subjected to heat. This work may also provide data for developing multiple techniques to control the emission of CPs and Cl-PAHs. Copyright © 2017 Elsevier Ltd. All rights reserved.

  1. Formation of chlorinated organic compounds in fluidized bed combustion of recycled fuels

    International Nuclear Information System (INIS)

    Vesterinen, R.; Kallio, M.; Kirjalainen, T.; Kolsi, A.; Merta, M.

    1997-01-01

    Four tests of co-combustion of recycled fuels (REP) with peat and coal in the 15 kW fluidized bed reactor were performed. The recycled fuel was so-called dry fraction in four vessels sampling at Keltinmaeki. In three tests a part of peat energy was replaced with coal. The mixtures were prepared so that in all mixtures 25 % of energy was recycled fuel and 75 % was either peat or the mixture of peat and coal. The concentrations of polyaromatic hydrocarbons (PAH), polychlorinated dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs) and chlorophenols decreased with increasing part of coal due to the increasing sulphur/chlorine ratio. Principal Component Analysis (PCA) and Partial Least Square regression analysis (PLS) showed that the chlorine, copper and sulphur contents of the fuel effected most on the concentrations of chlorophenols, chlorobenzenes, PCBs and PCDDs/PCDFs. Other variables influencing on a model were the lead concentration and the sulphur/chlorine ratio in fuel and the hydrogen chloride concentration of the flue gas. The concentrations of chlorophenols and chlorobenzenes were also significant for PCDD/PCDF concentrations in flue gas. The sulphur, chlorine, copper and chromium contents in fly ash and the temperature of the reactor influenced on the chlorophenol, chlorobenzene, PCB and PCDD/PCDF concentrations in fly ash. The chlorophenol and chlorobenzene contents in fly ash, the sulphur/chlorine ratio and the lead content in fuel, the sulphur dioxide, hydrogen chloride and carbon monoxide concentrations in flue gas had also influence on PCDD/PCDF concentrations in fly ash

  2. Dehalogenation of Chlorinated Hydroxybiphenyls by Fungal Laccase

    Science.gov (United States)

    Schultz, Asgard; Jonas, Ulrike; Hammer, Elke; Schauer, Frieder

    2001-01-01

    We have investigated the transformation of chlorinated hydroxybiphenyls by laccase produced by Pycnoporus cinnabarinus. The compounds used were transformed to sparingly water-soluble colored precipitates which were identified by gas chromatography-mass spectrometry as oligomerization products of the chlorinated hydroxybiphenyls. During oligomerization of 2-hydroxy-5-chlorobiphenyl and 3-chloro-4-hydroxybiphenyl, dechlorinated C—C-linked dimers were formed, demonstrating the dehalogenation ability of laccase. In addition to these nonhalogenated dimers, both monohalogenated and dihalogenated dimers were identified. PMID:11526052

  3. Radiolytic removal of trihalomethane in chlorinated seawater

    International Nuclear Information System (INIS)

    Rajamohan, R.; Rajesh, Puspalata; Venugopalan, V.P.; Rangarajan, S.; Natesan, Usha

    2015-01-01

    Biofouling is one of the major operational problems in seawater cooling systems. It is controlled by application of chlorine based biocides in the range of 0.5-2.0 mg L -1 . The bromide in seawater reacts with the added chlorine and forms hypobromous acid. The brominated residual biocides react with natural organic matter present in the seawater, resulting in the formation of trihalomethanes (THM) such as bromoform (CHBr 3 ), dibromochloromethane (CHBr 2 Cl) bromodichloromethane (CHBrCl 2 ). Though THMs represent a small fraction of the added chlorine, they are relatively more persistent than residual chlorine, and hence pose a potential hazard to marine life because of their reported mutagenicity. There have been few reports on removal of THMs from chlorinated seawater. In this work, the efficacy of gamma irradiation technique for the removal of THMs from chlorine-dosed seawater was investigated. Experiments were carried out using seawater collected from Kalpakkam. Irradiation study was conducted in chlorinated (1, 3, and 5 mg L -1 of Cl 2 ) seawater by applying various dosages (0.4-5.0 kGy) of gamma radiation using a 60 Co Gamma Chamber 5000. Bromoform showed a faster rate of degradation as compared to other halocarbons like bromodichloromethane and dibromochloromethane. This shows the change in total THM concentration with variation in the radiation dose and initial Cl 2 dosing. When the percentage degradation of all the three trihalomethane species was compared with applied doses, it was found that the maximum reduction occurred at a dose of 2.5 kGy. The reduction was almost similar for all the three doses (1, 3, 5 ppm of Cl 2 ) used for chlorination. With a further increase in radiation dose to 5.0 kGy, a slight increase in reduction was observed

  4. Stratospheric chlorine: Blaming it on nature

    International Nuclear Information System (INIS)

    Taube, G.

    1993-01-01

    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

  5. Dietary risk evaluation for 28 polycyclic aromatic hydrocarbons (PAHs) in tea preparations made of teas available on the Polish retail market.

    Science.gov (United States)

    Roszko, Marek; Kamińska, Marta; Szymczyk, Krystyna; Jędrzejczak, Renata

    2018-01-02

    The aim of this work was to assess dietary risk resulting from consumption of polycyclic aromatic hydrocarbons (PAHs) with tea infusions. To this end, levels of 28 PAHs in black, green, red and white teas available on the Polish retail market have been assessed. Profiles and correlation between concentrations of individual PAHs have been identified. A model study on transfer of PAHs from tea leaves into tea preparations has been conducted. Relatively high concentrations of 28 evaluated PAHs have been found in 58 tested samples of black, green, red and white teas sampled on the Polish retail market. Total concentration ∑28PAH ranged from 57 to 696 µg kg -1 with mean 258 µg kg -1 (dry tea leaves). The most mature tea leaves fermented to a small degree contained relatively the highest PAH levels among all four tested tea types. Relatively low PAH transfer rates into tea infusions and limited volumes of the consumed tea keep the risks associated with PAH dietary intake at a safely low level. The worst-case scenario dietary intake values were 7.62/0.82/0.097 ng kg -1 b.w. day -1 (estimated on the basis of the maximum found concentrations 696/113/23 µg kg -1 and maximum observed transfer rates 24/16/9%) for ∑28PAH/∑PAH4/B[a]P, respectively. MOE values calculated using the above worst case estimates exceeded 700,000 and 400,000 (BMDL 10 0.07 and 0.34 mg kg -1 b.w. day -1 ) for B[a]P and PAH4, respectively. Both B[a]P and PAH4 concentrations may be used as indicators of total PAH concentration in tea leaves; PAH4 slightly better fits low molecular weight PAHs. Several correlations between various PAHs/groups of PAHs have been identified, the strongest one (R 2 = 0.92) between PAH4 and EU PAH 15+1.

  6. Hydrocarbon Rocket Technology Impact Forecasting

    Science.gov (United States)

    Stuber, Eric; Prasadh, Nishant; Edwards, Stephen; Mavris, Dimitri N.

    2012-01-01

    Ever since the Apollo program ended, the development of launch propulsion systems in the US has fallen drastically, with only two new booster engine developments, the SSME and the RS-68, occurring in the past few decades.1 In recent years, however, there has been an increased interest in pursuing more effective launch propulsion technologies in the U.S., exemplified by the NASA Office of the Chief Technologist s inclusion of Launch Propulsion Systems as the first technological area in the Space Technology Roadmaps2. One area of particular interest to both government agencies and commercial entities has been the development of hydrocarbon engines; NASA and the Air Force Research Lab3 have expressed interest in the use of hydrocarbon fuels for their respective SLS Booster and Reusable Booster System concepts, and two major commercially-developed launch vehicles SpaceX s Falcon 9 and Orbital Sciences Antares feature engines that use RP-1 kerosene fuel. Compared to engines powered by liquid hydrogen, hydrocarbon-fueled engines have a greater propellant density (usually resulting in a lighter overall engine), produce greater propulsive force, possess easier fuel handling and loading, and for reusable vehicle concepts can provide a shorter turnaround time between launches. These benefits suggest that a hydrocarbon-fueled launch vehicle would allow for a cheap and frequent means of access to space.1 However, the time and money required for the development of a new engine still presents a major challenge. Long and costly design, development, testing and evaluation (DDT&E) programs underscore the importance of identifying critical technologies and prioritizing investment efforts. Trade studies must be performed on engine concepts examining the affordability, operability, and reliability of each concept, and quantifying the impacts of proposed technologies. These studies can be performed through use of the Technology Impact Forecasting (TIF) method. The Technology Impact

  7. SERDP/ESTCP Expert Panel Workshop on Research and Development Needs for Cleanup of Chlorinated Solvent Sites

    National Research Council Canada - National Science Library

    2001-01-01

    ...) perform its mission. These programs together conducted an expert panel workshop on August 6-7, 2001 to evaluate the needs for research and development in the general area of chlorinated solvent site cleanup...

  8. Chlorinated Flavonoids Modulate the Inflammatory Process in Human Blood.

    Science.gov (United States)

    Proença, Carina; Ribeiro, Daniela; Soares, Tânia; Tomé, Sara M; Silva, Artur M S; Lima, José L F C; Fernandes, Eduarda; Freitas, Marisa

    2017-08-01

    Flavonoids are known to react with neutrophil-generated hypochlorous acid (HOCl) at inflammation loci to form stable mono- and dichlorinated products. Some of these products have been shown to retain or even enhance their inflammatory potential, but further information is required in a broader approach to inflammatory mechanisms. In that sense, we performed an integrated evaluation on the anti-inflammatory potential of a panel of novel chlorinated flavonoids and their parent compounds, in several steps of the complex inflammatory cascade, namely, in the activity of cyclooxygenase (COX)-1 and COX-2, and in the production of cytokines [interleukin (IL)-6, IL-1β, tumor necrosis factor (TNF)], and the chemokine, IL-8, as well as in the production of reactive species, using human whole blood as a representative in vitro model, establishing, whenever possible, a structure-activity relationship. Although luteolin was the most active compound, chlorinated flavonoids demonstrated a remarkable pattern of activity for the resolution of the inflammatory processes. Our results demonstrated that 6-chloro-3',4',5,7-tetrahydroxyflavone deserves scientific attention due to its ability to modulate the reactive species and cytokines/chemokine production. In this regard, the therapeutic potential of flavonoids' metabolites, and in this particular case the chlorinated flavonoids, should not be neglected.

  9. Biological instability in a chlorinated drinking water distribution network.

    Science.gov (United States)

    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.

  10. Coupling of separation and reaction in zeolite membrane reactor for hydroisomerization of hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Gora, L.; Maloncy, M.L.; Jansen, J.C. [Ceramic Membrane Centre, The Pore, DelftChemTech, Delft Univ. of Technology (Netherlands)

    2004-07-01

    A zeolite membrane reactor has been developed for the hydroisomerization of hydrocarbons, in which the linear molecules are separated from branch ones on the silicalite-1 membrane prior to conversion of the permeated linear hydrocarbons to equilibrium levels on the catalyst bed. A model studies using C6 components are conduct. Separated n-C6 from 2MP (selectivity 24) is converted for 72% with 36% selectivity towards di-branched isomers (at 393 K). The results indicate that platinum containing chlorinated alumina/silicalite-1 membrane reactor has a potential in upgrading octane values and offers advantages such as higher efficiency, better process control and lower consumption of energy. (orig.)

  11. Spectrometric methods for the determination of chlorine in crude oil and petroleum derivatives — A review

    International Nuclear Information System (INIS)

    Doyle, Adriana; Saavedra, Alvaro; Tristão, Maria Luiza B.; Mendes, Luiz A.N.; Aucélio, Ricardo Q.

    2013-01-01

    Chlorine determination in crude oil is made in order to guarantee that the oil does not contain levels of this element that might cause damages in the oil processing equipment. In petroleum products, the determination of chlorine is made, for instance, to evaluate if there are proper concentrations of organochloride compounds, which are used as additives. Such determinations are currently performed following official guidelines from the ASTM International and from the United States Environmental Protection Agency as well as protocols indicated by the Universal Oil Products. X-ray fluorescence spectroscopy plays an important role in many of these official methods. In contrast, other spectrometric methods based on optical and mass detection are plagued by limitations related to both the fundamental characteristics of non-metals and to the complex sample matrices, which reflects in the small number of articles devoted to these applications. In this review, the current status of the spectrometric methods, especially the role played by X-ray fluorescence spectrometry, is evaluated in terms of the determination of chlorine in crude oil and petroleum derivatives. Comparison of the performance of the methods, limitations and potential new approaches to ensure proper spectrometric determinations of chlorine is indicated. - Highlights: • Critical evaluation of spectrometric methods for chlorine in petroleum products. • Reviews on element determination in petroleum have not address the case of chlorine. • Peculiarities of the spectrometric determination of Cl in petroleum are discussed. • The spectrometric approaches are detailed and compared to the official methods. • New trends in chlorine determination in petroleum products are indicated

  12. New model of chlorine-wall reaction for simulating chlorine concentration in drinking water distribution systems.

    Science.gov (United States)

    Fisher, Ian; Kastl, George; Sathasivan, Arumugam

    2017-11-15

    Accurate modelling of chlorine concentrations throughout a drinking water system needs sound mathematical descriptions of decay mechanisms in bulk water and at pipe walls. Wall-reaction rates along pipelines in three different systems were calculated from differences between field chlorine profiles and accurately modelled bulk decay. Lined pipes with sufficiently large diameters (>500 mm) and higher chlorine concentrations (>0.5 mg/L) had negligible wall-decay rates, compared with bulk-decay rates. Further downstream, wall-reaction rate consistently increased (peaking around 0.15 mg/dm 2 /h) as chlorine concentration decreased, until mass-transport to the wall was controlling wall reaction. These results contradict wall-reaction models, including those incorporated in the EPANET software, which assume wall decay is of either zero-order (constant decay rate) or first-order (wall-decay rate reduces with chlorine concentration). Instead, results are consistent with facilitation of the wall reaction by biofilm activity, rather than surficial chemical reactions. A new model of wall reaction combines the effect of biofilm activity moderated by chlorine concentration and mass-transport limitation. This wall reaction model, with an accurate bulk chlorine decay model, is essential for sufficiently accurate prediction of chlorine residuals towards the end of distribution systems and therefore control of microbial contamination. Implementing this model in EPANET-MSX (or similar) software enables the accurate chlorine modelling required for improving disinfection strategies in drinking water networks. New insight into the effect of chlorine on biofilm can also assist in controlling biofilm to maintain chlorine residuals. Copyright © 2017 Elsevier Ltd. All rights reserved.

  13. Studies concerning thermodynamics and kinetics of the absorption of halogenated hydrocarbons relevant to environment

    International Nuclear Information System (INIS)

    Weisweiler, W.; Eidam, K.; Winterbauer, H.

    1993-07-01

    In the context of the research project the scrubbing of air contaminated by peculiar volatile organic compounds was investigated using the absorption technique by means of high boiling organics as washing liquids. Eight chlorinated hydrocarbons well known from technical processes were chosen to be representative for the volatile organic compounds. Eleven absorption media were selected on the basis of their physical properties. For the determination of the solubility data of the absorption media due to chlorinated hydrocarbons, nitrogen as well as a mixture of nitrogen and oxygen were used as carrier gas. The influence of the dipole moment of the absorption media on the amount of solubility - expressed as enrichment factor - was studied, too. Concerning the technical application, the thermostability and the stability against diluted inorganic acids were studied as well. (orig.). 56 figs., 8 tabs., 63 refs [de

  14. Comparative evaluation of GHG emissions from the use of Miscanthus for bio-hydrocarbon production via fast pyrolysis and bio-oil upgrading

    International Nuclear Information System (INIS)

    Shemfe, Mobolaji B.; Whittaker, Carly; Gu, Sai; Fidalgo, Beatriz

    2016-01-01

    Highlights: • GHG emissions from the upgrading of pyrolysis-derived bio-oil is quantified.. • Soil organic carbon sequestration rate had a significant effect on GHG emission. • Increasing plant scale could improve the environmental performance of the system. • Nitrogen to the pyrolysis reactor had significant impact on GHG emissions. - Abstract: This study examines the GHG emissions associated with producing bio-hydrocarbons via fast pyrolysis of Miscanthus. The feedstock is then upgraded to bio-oil products via hydroprocessing and zeolite cracking. Inventory data for this study were obtained from current commercial cultivation practices of Miscanthus in the UK and state-of-the-art process models developed in Aspen Plus®. The system boundary considered spans from the cultivation of Miscanthus to conversion of the pyrolysis-derived bio-oil into bio-hydrocarbons up to the refinery gate. The Miscanthus cultivation subsystem considers three scenarios for soil organic carbon (SOC) sequestration rates. These were assumed as follows: (i) excluding (SOC), (ii) low SOC and (iii) high (SOC) for best and worst cases. Overall, Miscanthus cultivation contributed moderate to negative values to GHG emissions, from analysis of excluding SOC to high SOC scenarios. Furthermore, the rate of SOC in the Miscanthus cultivation subsystem has significant effects on total GHG emissions. Where SOC is excluded, the fast pyrolysis subsystem shows the highest positive contribution to GHG emissions, while the credit for exported electricity was the main ‘negative’ GHG emission contributor for both upgrading pathways. Comparison between the bio-hydrocarbons produced from the two upgrading routes and fossil fuels indicates GHG emission savings between 68% and 87%. Sensitivity analysis reveals that bio-hydrocarbon yield and nitrogen gas feed to the fast pyrolysis reactor are the main parameters that influence the total GHG emissions for both pathways.

  15. Process for desulfurizing hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    1937-04-12

    A process is described for the desulfurization of a mixture of hydrocarbons, and in particular hydrocarbons containing less than 7 atoms of carbon and sulfur compounds of the type of sulfur carbonyl, characterized by the fact that the mixture, preferably in the liquid phase, is brought in contact with a solution of caustic alkali, essentially anhydrous or preferably with a solution of alkali hydroxide in an organic hydroxy nonacid solvent, for example, an alcohol, or with an alkaline alcoholate, under conditions suitable to the formation of hydrogen sulfide which produces a hydrocarbon mixture free from sulfur compounds of the sulfur carbonyl type but containing hydrogen sulfide, and that it is treated, following mixing, having beem submitted to the first treatment, by means of aqueous alkaline hydroxide to eliminate the hydrogen sulfide.

  16. Estimation of optimum experimental parameters in chlorination of UO2 with Cl2 gas and carbon for UCl4

    International Nuclear Information System (INIS)

    Yang, Y.S.; Kang, Y.H.; Lee, H.K.

    1997-01-01

    For the preparation of uranium tetrachloride, the chlorination of UO 2 was carried out and an appropriate reaction system was confirmed. The effects of reaction temperature, time, injection ratio of N 2 gas and appropriate amount of carbon using a reductant on the conversion ratio and volatilization were evaluated. The optimum reaction time and temperature in chlorination of UO 2 for the preparation of UCl 4 were 2 h and 500-700 C, respectively. Also 50% of N 2 gas in chlorine gas proved to be the appropriate injection ratio. (orig.)

  17. Recovery of hydrocarbon oils

    Energy Technology Data Exchange (ETDEWEB)

    1941-02-10

    A process is disclosed for recovery of hydrocarbon oils, especially lubricating oils or diesel oils, through pressure hydrogenation of distillation, extraction of hydrogenation products from coal or coaly materials or from oils such as mineral oils or tars in liquid phase by use in a reaction vessel of fixed-bed catalysts, characterized in that as starting material is employed material which has been freed of asphaltic and resinous material by hydrogenation refining, vacuum-steam distillation, treatment with hydrogen-rich hydrocarbons (hydroforming), or sulfuric acid.

  18. CHLORINE ABUNDANCES IN COOL STARS

    Energy Technology Data Exchange (ETDEWEB)

    Maas, Z. G.; Pilachowski, C. A. [Indiana University Bloomington, Astronomy Department, Swain West 319, 727 East Third Street, Bloomington, IN 47405-7105 (United States); Hinkle, K., E-mail: zmaas@indiana.edu, E-mail: cpilacho@indiana.edu, E-mail: hinkle@noao.edu [National Optical Astronomy Observatory, P.O. Box 26732, Tucson, AZ 85726 (United States)

    2016-12-01

    Chlorine abundances are reported in 15 evolved giants and 1 M dwarf in the solar neighborhood. The Cl abundance was measured using the vibration-rotation 1-0 P8 line of H{sup 35}Cl at 3.69851 μ m. The high-resolution L -band spectra were observed using the Phoenix infrared spectrometer on the Kitt Peak Mayall 4 m telescope. The average [{sup 35}Cl/Fe] abundance in stars with −0.72 < [Fe/H] < 0.20 is [{sup 35}Cl/Fe] = (−0.10 ± 0.15) dex. The mean difference between the [{sup 35}Cl/Fe] ratios measured in our stars and chemical evolution model values is (0.16 ± 0.15) dex. The [{sup 35}Cl/Ca] ratio has an offset of ∼0.35 dex above model predictions, suggesting that chemical evolution models are underproducing Cl at the high metallicity range. Abundances of C, N, O, Si, and Ca were also measured in our spectral region and are consistent with F and G dwarfs. The Cl versus O abundances from our sample match Cl abundances measured in planetary nebula and H ii regions. In one star where both H{sup 35}Cl and H{sup 37}Cl could be measured, a {sup 35}Cl/{sup 37}Cl isotope ratio of 2.2 ± 0.4 was found, consistent with values found in the Galactic ISM and predicted chemical evolution models.

  19. Effect of chlorination on the development of marine biofilms dominated by diatoms

    Digital Repository Service at National Institute of Oceanography (India)

    Patil, J.S.; Jagadeesan, V.

    , and Thalassionema did not increase in density after chlorine treatment. It was also demonstrated that diatoms can colonize, grow and photosynthesize on chlorine-treated surfaces. Under pulse chlorination (treatment every 6 h), irrespective of chlorine concentration...

  20. Chlorination of organophosphorus pesticides in natural waters

    Energy Technology Data Exchange (ETDEWEB)

    Acero, Juan L. [Departamento de Ingenieria Quimica y Energetica, Universidad de Extremadura, 06071 Badajoz (Spain)], E-mail: jlacero@unex.es; Benitez, F. Javier; Real, Francisco J.; Gonzalez, Manuel [Departamento de Ingenieria Quimica y Energetica, Universidad de Extremadura, 06071 Badajoz (Spain)

    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 {sup o}C and pH 7 were determined to be 110.9, 0.004 and 191.6 M{sup -1} s{sup -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{sup -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.

  1. Chlorination of organophosphorus pesticides in natural waters

    International Nuclear Information System (INIS)

    Acero, Juan L.; Benitez, F. Javier; Real, Francisco J.; Gonzalez, Manuel

    2008-01-01

    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 o 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

  2. Automatic analyzing device for chlorine ion

    International Nuclear Information System (INIS)

    Sugibayashi, Shinji; Morikawa, Yoshitake; Fukase, Kazuo; Kashima, Hiromasa.

    1997-01-01

    The present invention provides a device of automatically analyzing a trance amount of chlorine ions contained in feedwater, condensate and reactor water of a BWR type power plant. Namely, zero-adjustment or span calibration in this device is conducted as follows. (1) A standard chlorine ion liquid is supplied from a tank to a mixer by a constant volume pump, and the liquid is diluted and mixed with purified water to form a standard liquid. (2) The pH of the standard liquid is adjusted by a pH adjuster. (3) The standard liquid is supplied to an electrode cell to conduct zero adjustment or span calibration. Chlorine ions in a specimen are measured by the device of the present invention as follows. (1) The specimen is supplied to a head tank through a line filter. (2) The pH of the specimen is adjusted by a pH adjuster. (3) The specimen is supplied to an electrode cell to electrically measure the concentration of the chlorine ions in the specimen. The device of the present invention can automatically analyze trance amount of chlorine ions at a high accuracy, thereby capable of improving the sensitivity, reducing an operator's burden and radiation exposure. (I.S.)

  3. The study of chlorination of nickel oxide by chlorine and calcium chloride in the presence of active additives

    OpenAIRE

    Ilic, Ilija; Krstev, Boris; Stopic, Srecko; Cerovic, K

    1997-01-01

    Chlorination of nickel oxide by chlorine and calcium chloride in the presence of C, BaS and S were studied, both experimentally and theoretically. Chlorination of nickel oxide by chlorine was carried out in the temperature range 573-873 K and by calcium chloride in the temperature range 1023-1223 K. The results obtained of the chlorination of nickel oxide by chlorine showed that C has the strongest and S the weakest effect on the process. Addition of BaS has a favorable effect on the chlorina...

  4. Emissions of hydrocarbons from combustion of biofuels

    International Nuclear Information System (INIS)

    Olsson, Mona; Persson, Eva Marie.

    1991-10-01

    Evaluations and measurements of emissions of hydrocarbons from power plants with a capacity exceeding 1 MW using biofuels (wood fuels and peat) have been studied in order to identify and quantify the emissions of incompletely combusted hydrocarbons. The influence of the type of fuel and the combustion technology applied were also studied, using literature references. The report summarizes monitoring results from a number of plants using biofuels. The reported emissions from the different plants can not be compared as they are relatively few and the test results have been obtained under various conditions using different methods of testing and analysis. The methods used are often poorly documented in the studied reports. Few investigations of emissions of hydrocarbons from plants in the range of 1 to 10 MW have been carried out. The plant and the technology used are important factors determining the amount and type of emissions of hydrocarbons. Larger temporary emissions can occur during start up, operational disturbances or when using fuel of inhomogeneous quality. In order to minimize the emissions the combustion process must be efficiently controlled, and a fuel of a hohogeneous quality must be used. The report also summarizes sampling and analysis methods used for monitoring emissions of hydrocarbons. (29 refs., 17 figs.)

  5. Non-destructive analysis of chlorine in fly ash cement concrete

    International Nuclear Information System (INIS)

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

    2009-01-01

    Preventive measures against reinforcement corrosion in concrete require increasing concrete density to prevent the diffusion of chloride ions to the steel surface. Pozzolanic materials, such as fly ash (FA), silica fume (SF), and blast furnace slag (BFS) are added to concrete to increase its density. Monitoring the chloride concentration in concrete is required to assess the chances of reinforcement corrosion. In this study, FA was added to Portland cement concrete to increase its density. Prompt gamma neutron activation analysis (PGNAA) technique was utilized to analyze the concentration of chlorine in concrete. The chlorine concentration in the FA cement concrete was evaluated by determining the yield of 1.16, 1.95, 6.11, 6.62, 7.41, 7.79, and 8.58 MeV gamma-rays of chlorine from the FA concrete specimen containing 0.4-3.5 wt% chlorine. An excellent agreement was noted between the experimental yield of the prompt gamma-rays and the calculated yield obtained through the Monte Carlo simulations. The Minimum Detectable Concentration (MDC) of chlorine in FA cement concrete was also calculated. The best value of MDC limit of chlorine in the FA cement concrete was found to be 0.022±0.007 and 0.038±0.017 wt% for 1.16 and 6.11 MeV prompt gamma-rays, respectively. Within the statistical uncertainty, the lower bound of MDC meets the maximum permissible limit of 0.03 wt% of chlorine in concrete set by American Concrete Institute Committee 318.

  6. Non-destructive analysis of chlorine in fly ash cement concrete

    Energy Technology Data Exchange (ETDEWEB)

    Naqvi, A.A. [Department of Physics, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia)], E-mail: aanaqvi@kfupm.edu.sa; Garwan, M.A.; Nagadi, M.M. [Department of Physics, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Maslehuddin, M. [Center for Engineering Research, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Al-Amoudi, O.S.B. [Department of Civil Engineering, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Khateeb-ur-Rehman [Department of Physics, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia)

    2009-08-11

    Preventive measures against reinforcement corrosion in concrete require increasing concrete density to prevent the diffusion of chloride ions to the steel surface. Pozzolanic materials, such as fly ash (FA), silica fume (SF), and blast furnace slag (BFS) are added to concrete to increase its density. Monitoring the chloride concentration in concrete is required to assess the chances of reinforcement corrosion. In this study, FA was added to Portland cement concrete to increase its density. Prompt gamma neutron activation analysis (PGNAA) technique was utilized to analyze the concentration of chlorine in concrete. The chlorine concentration in the FA cement concrete was evaluated by determining the yield of 1.16, 1.95, 6.11, 6.62, 7.41, 7.79, and 8.58 MeV gamma-rays of chlorine from the FA concrete specimen containing 0.4-3.5 wt% chlorine. An excellent agreement was noted between the experimental yield of the prompt gamma-rays and the calculated yield obtained through the Monte Carlo simulations. The Minimum Detectable Concentration (MDC) of chlorine in FA cement concrete was also calculated. The best value of MDC limit of chlorine in the FA cement concrete was found to be 0.022{+-}0.007 and 0.038{+-}0.017 wt% for 1.16 and 6.11 MeV prompt gamma-rays, respectively. Within the statistical uncertainty, the lower bound of MDC meets the maximum permissible limit of 0.03 wt% of chlorine in concrete set by American Concrete Institute Committee 318.

  7. Optrode for sensing hydrocarbons

    Science.gov (United States)

    Miller, H.; Milanovich, F.P.; Hirschfeld, T.B.; Miller, F.S.

    1988-09-13

    A two-phase system employing the Fujiwara reaction is provided for the fluorometric detection of halogenated hydrocarbons. A fiber optic is utilized to illuminate a column of pyridine trapped in a capillary tube coaxially attached at one end to the illuminating end of the fiber optic. A strongly alkaline condition necessary for the reaction is maintained by providing a reservoir of alkali in contact with the column of pyridine, the surface of contact being adjacent to the illuminating end of the fiber optic. A semipermeable membrane caps the other end of the capillary tube, the membrane being preferentially permeable to the halogenated hydrocarbon and but preferentially impermeable to water and pyridine. As the halogenated hydrocarbon diffuses through the membrane and into the column of pyridine, fluorescent reaction products are formed. Light propagated by the fiber optic from a light source, excites the fluorescent products. Light from the fluorescence emission is also collected by the same fiber optic and transmitted to a detector. The intensity of the fluorescence gives a measure of the concentration of the halogenated hydrocarbons. 5 figs.

  8. Catalyst for hydrocarbon conversion

    International Nuclear Information System (INIS)

    Duhaut, P.; Miquel, J.

    1975-01-01

    A description is given for a catalyst and process for hydrocarbon conversions, e.g., reforming. The catalyst contains an alumina carrier, platinum, iridium, at least one metal selected from uranium, vanadium, and gallium, and optionally halogen in the form of metal halide of one of the aforesaid components. (U.S.)

  9. Chlorine-rich plasma polymer coating for the prevention of attachment of pathogenic fungal cells onto materials surfaces

    International Nuclear Information System (INIS)

    Lamont-Friedrich, Stephanie J; Michl, Thomas D; Giles, Carla; Griesser, Hans J; Coad, Bryan R

    2016-01-01

    The attachment of pathogenic fungal cells onto materials surfaces, which is often followed by biofilm formation, causes adverse consequences in a wide range of areas. Here we have investigated the ability of thin film coatings from chlorinated molecules to deter fungal colonization of solid materials by contact killing of fungal cells reaching the surface of the coating. Coatings were deposited onto various substrate materials via plasma polymerization, which is a substrate-independent process widely used for industrial coating applications, using 1,1,2-trichloroethane as the process vapour. XPS surface analysis showed that the coatings were characterized by a highly chlorinated hydrocarbon polymer nature, with only a very small amount of oxygen incorporated. The activity of these coatings against human fungal pathogens was quantified using a recently developed, modified yeast assay and excellent antifungal activity was observed against Candida albicans and Candida glabrata . Plasma polymer surface coatings derived from chlorinated hydrocarbon molecules may therefore offer a promising solution to preventing yeast and mould biofilm formation on materials surfaces, for applications such as air conditioners, biomedical devices, food processing equipment, and others. (paper)

  10. Effects of aging on chlorinated plasma polymers

    Energy Technology Data Exchange (ETDEWEB)

    Turri, Rafael Gustavo; Amorim, Milena Kowalczuk Manosso; Hadich, Tayan Vieira; Fernandes, Isabela Cristina; Fernandes, Gabriel Ferreira; Rossi, Diego; Rangel, Elidiane Cipriano; Durrant, Steven Frederick, E-mail: steve@sorocaba.unesp.br [Universidade Estadual Paulista Julio de Mesquita Filho (UNESP), Sorocaba, SP (Brazil). Lab. de Plasmas Tecnologicos

    2017-07-15

    Thin films deposited from propanol-chloroform-argon mixtures by plasma enhanced chemical vapor deposition at different partial pressures of chloroform in the feed, C{sub Cl}, were characterized after two years of aging and their characteristics compared with their as-deposited properties. Film thickness decreased and surface roughness increased with aging. Surface contact angles also increased with aging for the chlorinated films. For the film deposited with 40% chloroform in the feed the contact angle increased about 14°. Transmission infrared and Energy dispersive X-ray spectroscopy revealed that the films gain carbonyl and hydroxyl groups and lose chlorine and hydrogen on aging. Chlorination appears to make the films more durable. Delamination was observed for the unchlorinated films. (author)

  11. Investigation of molybdenum pentachloride interaction with chlorine

    International Nuclear Information System (INIS)

    Salyulev, A.B.; Vovkotrub, Eh.G.; Strekalovskij, V.N.

    1993-01-01

    In Raman spectra of molybdenum pentachloride solutions in liquid chlorine lines were recorded in case of 397, 312, 410, 217 and 180 cm - 1 vibrations of ν 1 (A 1 '), ν 2 (A 1 '), ν 5 (E'), ν 6 (E') and ν 8 (E'') monomer (symmetry D 3h ) molecules of MoCl 5 . Interaction of molten molybdenum pentachloride with chlorine at increased (up to 6 MPa) pressures of Cl 2 was studied. In Raman spectra of its vapour distillation in liquid chlorine alongside with MoCl 5 lines appearance of new lines at 363 and 272 cm -1 , similar in their frequency to the ones calculated for the vibrations ν 1 (A 1g ) and ν 2 (E g ) of MoCl 6 molecules (symmetry O h ), was observed

  12. Blends of caprolactam/caprolactone copolymers and chlorinated polymers

    NARCIS (Netherlands)

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

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

  13. Chlorine isotopes potential as geo-chemical tracers

    Digital Repository Service at National Institute of Oceanography (India)

    Shirodkar, P.V.; Pradhan, U.K.; Banerjee, R.

    The potential of chlorine isotopes as tracers of geo-chemical processes of earth and the oceans is highlighted based on systematic studies carried out in understanding the chlorine isotope fractionation mechanism, its constancy in seawater and its...

  14. Chlorin derivatives for potential use in BNCT

    International Nuclear Information System (INIS)

    Osterloh, J.; Neumann, M.; Ruf, S.; Gabel, D.

    2000-01-01

    A series of BSH containing alkyl ether homologues of pytropheophorbide a has been prepared. Cellular uptake studies show that is possible to accumulate 2.2 mg of the heptyl ether after 2 h of incubation with a 0.04 mM solution. That means a boron amount of 330 μg per gram cell mass. Cytotoxicity studies allow radiobiological experiments. The patterns of subcellular localisation visualised by fluorescence microscopy and CLSM show that much of the chlorins is located close to the nucleus and in the nucleus membrane. However, no chlorin was found in the nucleus. (author)

  15. Chlorinated tyrosine derivatives in insect cuticle

    DEFF Research Database (Denmark)

    Andersen, Svend Olav

    2004-01-01

    A method for quantitative measurement of 3-monochlorotyrosine and 3,5-dichlorotyrosine in insect cuticles is described, and it is used for determination of their distribution in various cuticular regions in nymphs and adults of the desert locust, Schistocerca gregaria. The two chlorinated tyrosine......, not-yet sclerotized cuticle of adult femur and tibia, the amounts increased rapidly during the first 24 h after ecdysis and more slowly during the next two weeks. Control analyses using stable isotope dilution mass spectrometry have confirmed that the chlorinated tyrosines are not artifacts formed...

  16. Determination of carbon chlorine and fluorine in uranium dioxide

    International Nuclear Information System (INIS)

    Kijko, N.I.; Timofeev, G.A.

    1983-01-01

    Techniques of chlorine and fluorine determination and simultaneous determination of carbon and chlorine in electrolytic uranium dioxide are described. The method of chlorine and fluorine determination is based on their separation during oxide pyrohydrolysis with subsequent spectrophotometric analysis of condensate. Lower determination limits constitute 1 μg for chlorine, 0.5 μg for fluorine. Relative standard deviation when the content of impurities analyzed is 10 -3 % constitutes 0.05-0.07

  17. Historical and Retrospective Survey of Monitored Natural Attenuation: A Line of Inquiry Supporting Monitored Natural Attenuation and Enhanced Passive Remediation of Chlorinated Solvents

    International Nuclear Information System (INIS)

    LOONEY, BB.

    2004-01-01

    As requested by the Savannah River Technology Center, Groundwater Services, Inc. (GSI), has conducted a historical analysis of Monitored Natural Attenuation (MNA) application at chlorinated solvent sites. The objective of the analysis was to document trends, characteristics, successes, and barriers in the use of MNA as a remedy at chlorinated solvent sites. The analysis consisted of the following: (1) a review of recent literature regarding application of natural attenuation at chlorinated solvent sites, (2) a review of regulatory and industry guidance directing evaluation and implementation of MNA as a remedy at chlorinated solvent sites, and (3) a historical survey distributed to MNA experts, which requested data relating to the evaluation and implementation of MNA at chlorinated solvent sites

  18. 21 CFR 177.2430 - Polyether resins, chlorinated.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyether resins, chlorinated. 177.2430 Section 177... Components of Articles Intended for Repeated Use § 177.2430 Polyether resins, chlorinated. Chlorinated polyether resins may be safely used as articles or components of articles intended for repeated use in...

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

    Science.gov (United States)

    Adira Wan Khalit, Wan Nor; Tay, Kheng Soo

    2016-05-18

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

  20. Natural and Enhanced Attenuation of Chlorinated Solvents Using RT3D

    Energy Technology Data Exchange (ETDEWEB)

    Johnson, Christian D.; Truex, Michael J.; Clement, T P.

    2006-07-25

    RT3D (Reactive Transport in 3-Dimensions) is a reactive transport code that can be applied to model solute fate and transport for many different purposes. This document specifically addresses application of RT3D for modeling related to evaluation and implementation of Monitored Natural Attenuation (MNA). Selection of MNA as a remedy requires an evaluation process to demonstrate that MNA will meet the remediation goals. The U.S. EPA, through the Office of Solid Waste and Emergency Response (OSWER) Directive 9200.4?17P, provides the regulatory context for the evaluation and implementation of MNA. In a complementary fashion, the context for using fate and transport modeling as part of MNA evaluation is described in the EPA?s technical protocol for chlorinated solvent MNA, the Scenarios Evaluation Tool for Chlorinated Solvent MNA, and in this document. The intent of this document is to describe (1) the context for applying RT3D for chlorinated solvent MNA and (2) the attenuation processes represented in RT3D, (3) dechlorination reactions that may occur, and (4) the general approach for using RT3D reaction modules (including a summary of the RT3D reaction modules that are available) to model fate and transport of chlorinated solvents as part of MNA or for combinations of MNA and selected types of active remediation.

  1. Total Petroleum Hydrocarbon Content (TPH) As an Index ...

    African Journals Online (AJOL)

    MICHAEL

    potential for hydrocarbon accumulation and could be evaluated for its efficacy as a tool in phytoremediation exercise for cleaning ... often assessed from changes in the physical, chemical ... Germination test: The approach adapted by Agboola.

  2. Soil microbial communities: Influence of geographic location and hydrocarbon pollutants

    CSIR Research Space (South Africa)

    Maila, MP

    2006-02-01

    Full Text Available The importance and relevance of the geographical origin of the soil sample and the hydrocarbons in determining the functional or species diversity within different bacterial communities was evaluated using the community level physiological profiles...

  3. Assessment of plant-derived hydrocarbons. Final report

    Energy Technology Data Exchange (ETDEWEB)

    McFadden, K.; Nelson, S.H.

    1981-09-30

    A number of hydrocarbon producing plants are evaluated as possible sources of rubber, liquid fuels, and industrial lubricants. The plants considered are Euphorbia lathyris or gopher plant, milkweeds, guayule, rabbit brush, jojoba, and meadow foam. (ACR)

  4. In situ experimental study for the optimization of chlorine dosage in seawater cooling systems

    Energy Technology Data Exchange (ETDEWEB)

    Nebot, E.; Casanueva, T.; Fernandez-Baston, M.M.; Sales, D. [Department of Chemical Engineering, Food Technology and Environmental Technologies, University of Cadiz (Spain); Casanueva, J.F. [Department of Thermal Engines, University of Cadiz (Spain)

    2006-11-15

    The paper details an in situ study for the evaluation of the evolution of fouling heat transfer resistance and to optimize the antifouling chlorine dosage at a 550MW power station. A portable pilot plant has been designed to simulate the steam surface condenser and used as an accurate fouling monitor that takes the seawater from the same intake point as the power station. This study includes fouling extraction and its characterization for different dosage patterns. The residual chlorine concentration at the cooling-water discharge from the power station is 0.2mg/l and has been considered appropriate for the prevention of the formation of fouling, because with this concentration approximately 90% reduction in the amount of fouling is obtained. Residual chlorine dosages lower than 0.2ppm could be effective in controlling fouling development if mechanical techniques of fouling control are also available. (author)

  5. Bioremediation of Petroleum Hydrocarbon Contaminated Sites

    Energy Technology Data Exchange (ETDEWEB)

    Fallgren, Paul

    2009-03-30

    Bioremediation has been widely applied in the restoration of petroleum hydrocarbon-contaminated. Parameters that may affect the rate and efficiency of biodegradation include temperature, moisture, salinity, nutrient availability, microbial species, and type and concentration of contaminants. Other factors can also affect the success of the bioremediation treatment of contaminants, such as climatic conditions, soil type, soil permeability, contaminant distribution and concentration, and drainage. Western Research Institute in conjunction with TechLink Environmental, Inc. and the U.S. Department of Energy conducted laboratory studies to evaluate major parameters that contribute to the bioremediation of petroleum-contaminated drill cuttings using land farming and to develop a biotreatment cell to expedite biodegradation of hydrocarbons. Physical characteristics such as soil texture, hydraulic conductivity, and water retention were determined for the petroleum hydrocarbon contaminated soil. Soil texture was determined to be loamy sand to sand, and high hydraulic conductivity and low water retention was observed. Temperature appeared to have the greatest influence on biodegradation rates where high temperatures (>50 C) favored biodegradation. High nitrogen content in the form of ammonium enhanced biodegradation as well did the presence of water near field water holding capacity. Urea was not a good source of nitrogen and has detrimental effects for bioremediation for this site soil. Artificial sea water had little effect on biodegradation rates, but biodegradation rates decreased after increasing the concentrations of salts. Biotreatment cell (biocell) tests demonstrated hydrocarbon biodegradation can be enhanced substantially when utilizing a leachate recirculation design where a 72% reduction of hydrocarbon concentration was observed with a 72-h period at a treatment temperature of 50 C. Overall, this study demonstrates the investigation of the effects of

  6. Distilling hydrocarbons, etc

    Energy Technology Data Exchange (ETDEWEB)

    Turner, C

    1917-11-23

    In the fractional or destructive distillation of hydrocarbon oils or other liquids, the pressure in the still is raised and lowered alternately. The still is closed to raise the pressure, and is opened to lower the pressure rapidly solely by expansion of the vapors. The operation is effected without intermittent cooling, except such as may occur during the lowering of the pressure. In distilling hydrocarbon oil, pressure steam is blown into the oil until the pressure reaches 5 lb/in./sup 2/. The vapor outlet is then opened until the pressure falls to 2 lb/in./sup 2/, whereupon the vapor outlet is closed and steam is again admitted. The operation is continued until the steam, which is of 20 lb pressure, no longer effects distillation; after this stage, superheated steam is used.

  7. Distilling hydrocarbon oils

    Energy Technology Data Exchange (ETDEWEB)

    Tausz, J

    1924-07-16

    Hydrocarbon oils such as petroleum, shale oils, lignite or coal tar oils are purified by distilling them and collecting the distillate in fractions within narrow limits so that all the impurities are contained in one or more of the narrow fractions. In distilling ligroin obtained by destructive distillation of brown coal, it is found that the coloring and resin-forming constituents are contained in the fractions distilling over at 62 to 86/sup 0/C and 108/sup 0/C. The ligroin is purified, therefore, by distillating in an apparatus provided with an efficient dephlegmotor and removing these two fractions. The distillation may be carried out wholly or in part under reduced pressure, and fractions separated under ordinary pressure may be subsequently distilled under reduced pressure. The hydrocarbons may be first separated into fractions over wider limits and the separate fractions be subjected to a further fractional distillation.

  8. 21 CFR 177.1610 - Polyethylene, chlorinated.

    Science.gov (United States)

    2010-04-01

    ... Chlorine in Vinyl Chloride Polymers and Copolymers,” which is incorporated by reference (Copies may be..., Philadelphia, PA 19428-2959, or may be examined at the National Archives and Records Administration (NARA). For... percent in plastic articles prepared from polyvinyl chloride and/or from vinyl chloride copolymers...

  9. 46 CFR 151.50-31 - Chlorine.

    Science.gov (United States)

    2010-10-01

    ... inside diameter manhole, fitted with a cover located above the maximum liquid level and as close as... accessary equipment shall be of a type suitable for use with chlorine and shall be made of metal, corrosion... shutoff valves and with safety relief valves. All valves shall be bolted to the cover or covers specified...

  10. Thermodynamic consideration on chlorination of uraniferous phosphorite

    International Nuclear Information System (INIS)

    Itagaki, Kimio; Tozawa, Kazuteru; Taki, Tomihiro; Hirono, Shuichiro.

    1989-01-01

    The uranium ore of low grade which has apatite as a main mineral, but is different from the phosphorite used as the raw material for phosphoric acid production, exists in large amount in South America and Africa continents, and the importance of its effective utilization as future uranium resources is recognized. The Power Reactor and Nuclear Fuel Development Corp. took up the establishment of the treatment techniques to make this ore into resources as the subject of a project, and proposed the process of volatilizing the uranium in the ore as the chloride and recovering it, and at present, it attempts the experiment on the chlorination treatment. In this paper, the thermodynamic examination on the feasibility of this process, the optimum condition for leaving calcium existing in a large amount in the ore as the phosphate without chlorination and recovering only uranium by chlorination and volatilization, the phase reaction equilibrium chart and the calculation method according to thermodynamics concerning the behavior of chlorination of accompanying elements such as iron, silicon and aluminum and the effect of moisture in the ore are reported. (K.I.)

  11. Nuclear explosives and hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Cohen, P

    1971-10-01

    A nuclear explosive 12 in. in diam and producing very little tritium is feasible in France. Such a device would be well adapted for contained nuclear explosions set off for the purpose of hydrocarbon storage or stimulation. The different aspects of setting off the explosive are reviewed. In the particular case of gas storage in a nuclear cavity in granite, it is demonstrated that the dose of irradiation received is extremely small. (18 refs.)

  12. Treatment of hydrocarbon oils

    Energy Technology Data Exchange (ETDEWEB)

    1936-02-22

    A process is described for refining a mixture of liquid hydrocarbons containing harmful substances, this process permitting the operation, which consists in treating the liquid mixture at a temperature higher than 200/sup 0/C with a solid catalyst of phosphoric acid, consisting of phosphoric acid deposited on a solid support of the type of metallurgical coke, for a time sufficient to convert the harmful components to inoffensive substances.

  13. Biogeochemistry of Halogenated Hydrocarbons

    Science.gov (United States)

    Adriaens, P.; Gruden, C.; McCormick, M. L.

    2003-12-01

    Halogenated hydrocarbons originate from both natural and industrial sources. Whereas direct anthropogenic emissions to the atmosphere and biosphere are often easy to assess, particularly when they are tied to major industrial activities, the attribution of emissions to other human activities (e.g., biomass burning), diffuse sources (e.g., atmospheric discharge, run off), and natural production (e.g., soils, fungi, algae, microorganisms) are difficult to quantify. The widespread occurrence of both alkyl and aryl halides in groundwater, surface water, soils, and various trophic food chains, even those not affected by known point sources, suggests a substantial biogeochemical cycling of these compounds (Wania and Mackay, 1996; Adriaens et al., 1999; Gruden et al., 2003). The transport and reactive fate mechanisms controlling their reactivity are compounded by the differences in sources of alkyl-, aryl-, and complex organic halides, and the largely unknown impact of biogenic processes, such as enzymatically mediated halogenation of organic matter, fungal production of halogenated hydrocarbons, and microbial or abiotic transformation reactions (e.g., Asplund and Grimvall, 1991; Gribble, 1996; Watling and Harper, 1998; Oberg, 2002). The largest source may be the natural halogenation processes in the terrestrial environment, as the quantities detected often exceed the amount that can be explained by human activities in the surrounding areas ( Oberg, 1998). Since biogeochemical processes result in the distribution of a wide range of halogenated hydrocarbon profiles, altered chemical structures, and isomer distributions in natural systems, source apportionment (or environmental forensics) can often only be resolved using multivariate statistical methods (e.g., Goovaerts, 1998; Barabas et al., 2003; Murphy and Morrison, 2002).This chapter will describe the widespread occurrence of halogenated hydrocarbons, interpret their distribution and biogeochemical cycling in light of

  14. Cracking hydrocarbon oils

    Energy Technology Data Exchange (ETDEWEB)

    Seigle, A A.F.M.

    1922-12-20

    Hydrocarbon oils such as petroleum, peat, shale, or lignite oils, heavy tars, resin oils, naphthalene oils, etc., are vaporized by being fed from a tank through a preheater to the lower part of a vertical annular retort heated by a flame projected down the central cavity from a burner. The oil vapors rise through annular passages formed by disks, on which are placed chips of copper, iron, aluminum, etc., to act as catalysts.

  15. High boiling point hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Pier, M

    1929-04-29

    A process is given for the production of hydrocarbons of high boiling point, such as lubricating oils, from bituminous substances, such as varieties of coal, shale, or other solid distillable carbonaceous materials. The process consists of treating the initial materials with organic solvents and then subjecting the products extracted from the initial materials, preferably directly, to a reducing treatment in respect to temperature, pressure, and time. The reduction treatment is performed by means of hydrogen under pressure.

  16. Direct hydrocarbon fuel cells

    Science.gov (United States)

    Barnett, Scott A.; Lai, Tammy; Liu, Jiang

    2010-05-04

    The direct electrochemical oxidation of hydrocarbons in solid oxide fuel cells, to generate greater power densities at lower temperatures without carbon deposition. The performance obtained is comparable to that of fuel cells used for hydrogen, and is achieved by using novel anode composites at low operating temperatures. Such solid oxide fuel cells, regardless of fuel source or operation, can be configured advantageously using the structural geometries of this invention.

  17. In-situ hydrocarbon delineation using laser-induced fluorescence

    International Nuclear Information System (INIS)

    Taer, A.D.; Hastings, R.W.; Brown, A.Y.; Frend, R.

    1996-01-01

    An investigation of hydrocarbons in soils was conducted at an active Shell Oil Company petroleum products terminal, located in Carson, California. An investigation approach involving Laser-Induced Fluorescence (LIF) and Cone Penetrometer Testing (CPT) technologies was implemented to provide real-time, in-situ characterization of site stratigraphy, hydrocarbon distribution and importantly, hydrocarbon product differentiation. The area of investigation is located along a property boundary, where a plume of separate phase hydrocarbons has been actively recovered for several years. CPT/LIF technology was selected for the investigation since previous delineation efforts using hydrocarbon fingerprinting methods proved inconclusive. Additionally, the CPT/LIF technology had the potential to provide a cost effective solution to accomplish project objectives. Based on the information obtained during this investigation, it was determined that the plume of separate phase hydrocarbons along the northern property boundary is from a source distinctly different than any identified hydrocarbons known to be from on-site sources. In addition, the plume was determined to not be connected with any other known on-site hydrocarbon plumes. The results of this CPT/LIF investigation were consistent with the known hydrogeologic conditions. This evaluation determined that CPT/LIF technology was very effective in addressing project objectives and resulted in a significant cost savings

  18. Inactivation Kinetics of the Cyanobacterial Toxin Microcystin-LR by Free Chlorine

    Science.gov (United States)

    Worldwide, the increasing occurrence of toxins produced by cyanobacteria in water bodies used as source waters for drinking water has become an important public health issue. Microcystin-LR is one of the most commonly found cyanotoxins. A detailed evaluation of the free chlorine ...

  19. Turbidity and chlorine demand reduction using alum and moringa flocculation before household chlorination in developing countries.

    Science.gov (United States)

    Preston, Kelsey; Lantagne, Daniele; Kotlarz, Nadine; Jellison, Kristen

    2010-03-01

    Over 1.1 billion people in the world lack access to improved drinking water. Diarrhoeal and other waterborne diseases cause an estimated 1.87 million deaths per year. The Safe Water System (SWS) is a household water treatment intervention that reduces diarrhoeal disease incidence among users in developing countries. Turbid waters pose a particular challenge to implementation of SWS programmes; although research shows that a 3.75 mg l(-1) sodium hypochlorite dose effectively treats turbid waters, users sometimes object to the strong chlorine taste and prefer to drink water that is more aesthetically pleasing. This study investigated the efficacy of two locally available chemical water treatments-alum and Moringa oleifera flocculation-to reduce turbidity and chlorine demand at turbidities of 10, 30, 70, 100 and 300 NTU. Both treatments effectively reduced turbidity (alum flocculation 23.0-91.4%; moringa flocculation 14.2-96.2%). Alum flocculation effectively reduced chlorine demand compared with controls at 30, 70, 100 and 300 NTU (p=0.01-0.06). Moringa flocculation increased chlorine demand to the point where adequate free chlorine residual was not maintained for 24 hours after treatment. Alum pretreatment is recommended in waters>or=30 NTU for optimum water disinfection. Moringa flocculation is not recommended before chlorination.

  20. A study on chlorination of uranium metal using ammonium chloride

    International Nuclear Information System (INIS)

    Eun, H.C.; Kim, T.J.; Jang, J.H.; Kim, G.Y.; Lee, S.J.; Hur, J.M.

    2017-01-01

    In this study, the chlorination of uranium metal using ammonium chloride (NH 4 Cl) was conducted to derive an easy and simple uranium chloride production method without impurities. In thermodynamic equilibrium calculations, it was predicted that only uranium chlorides can be produced by the reactions between uranium metal and NH 4 Cl. Experimental conditions for the chlorination of uranium metal were determined using a chlorination test of cerium metal using NH 4 Cl. It was confirmed that UCl 3 and UCl 4 in the form of particles as uranium chlorination products can be obtained from the chlorination method using NH 4 Cl. (author)

  1. Factors affecting hydrocarbon removal by air stripping

    International Nuclear Information System (INIS)

    McFarland, W.E.

    1992-01-01

    This paper includes an overview of the theory of air stripping design considerations and the factors affecting stripper performance. Effects of temperature, contaminant characteristics, stripping tower geometry and air/water ratios on removal performance are discussed. The discussion includes treatment of groundwater contaminated with petroleum hydrocarbons and chlorinated solvents such as TCE and PCE. Control of VOC emissions from air strippers has become a major concern in recent years, due to more stringent restrictions on air quality in many areas. This paper includes an overview of available technology to control air emissions (including activated carbon adsorption, catalytic oxidation and steam stripping) and the effects of air emission control on overall efficiency of the treatment process. The paper includes an overview of the relative performance of various packing materials for air strippers and explains the relative advantages and disadvantages of comparative packing materials. Field conditions affecting selection of packing materials are also discussed. Practical guidelines for the design of air stripping systems are presented, as well as actual case studies of full-scale air stripping projects

  2. Development of a Chlorine Dosing Strategy for Fresh Produce Washing Process to Maintain Microbial Food Safety and Minimize Residual Chlorine.

    Science.gov (United States)

    Chen, Xi; Hung, Yen-Con

    2018-05-22

    The residual free chlorine level in fresh produce wash solution is closely correlated to the chemical and microbial safety of produce. Excess amount of free chlorine can quickly react with organic matters to form hazardous disinfection by-products (DBPs) above EPA-permitted levels, whereas deficiency of residual chlorine in produce wash solution may result in incompletely removing pathogens on produce. The purpose of this study was to develop a chlorine dosing strategy to optimize the chlorine dosage during produce washing process without impacting the microbial safety of fresh produce. Prediction equations were developed to estimate free chlorine needed to reach targeted residual chlorine at various sanitizer pH and organic loads, and then validated using fresh-cut iceberg lettuce and whole strawberries in an automated produce washer. Validation results showed that equations successfully predicted the initial chlorine concentration needed to achieve residual chlorine at 10, 30, 60, and 90 mg/L for both lettuce and strawberry washing processes, with the root mean squared error at 4.45 mg/L. The Escherichia coli O157:H7 reductions only slightly increased on iceberg lettuce and strawberries with residual chlorine increasing from 10 to 90 mg/L, indicating that lowering residual chlorine to 10 mg/L would not compromise the antimicrobial efficacy of chlorine-based sanitizer. Based on the prediction equations and E. coli O157:H7 reduction results, a chlorine dosing strategy was developed to help the produce industry to maintain microbial inactivation efficacy without adding excess amount of free chlorine. The chlorine dosing strategy can be used for fresh produce washing process to enhance the microbial food safety and minimize the DBPs formation potential. © 2018 Institute of Food Technologists®.

  3. Toxic effects of chlorinated cake flour in rats.

    Science.gov (United States)

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

    1977-05-01

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

  4. Chlorine isotope fractionation during supergene enrichment of copper

    Science.gov (United States)

    Reich, M.; Barnes, J.; Barra, F.; Milojevic, C.; Drew, D.

    2017-12-01

    Supergene enrichment of Cu deposits in the Atacama Desert has played a critical role in making this the prime Cu-producing province of the world. The Cu-hydroxychloride atacamite is a major component of supergene zones in this region whereas in similar deposits elsewhere it is rare. Atacamite requires saline water to form and dissolves rapidly when exposed to fresh, meteoric water. Previous chlorine stable isotope data [1] for atacamite mineralization at the Radomiro Tomic, Chuquicamata and Mina Sur Cu deposits show δ37Cl values that range from -0.1 to +0.2‰, indicating a similar nonmagmatic source for the introduction of chloride. However, distal atacamite mineralization on the periphery of these orebodies show more fractionated and lighter δ37Cl values (-3.2 to -0.1‰). Although little disagreement currently exists about the involvement of saline groundwater during the formation of atacamite [2], no δ37Cl data are currently available for atacamite within a single deposit and/or supergene enrichment profile that allow explaining the aforementioned differences in the observed δ37Cl values. Furthermore, no experimental data for chlorine isotope fractionation between Cu-hydroxychloride minerals and water exist that help evaluate possible mechanisms of fractionation along the groundwater flow path. Here we present a new database that combines detailed mineralogical observations with δ37Cl data of atacamite along a thick ( 100 m) supergene enrichment profile at the Barreal Seco IOCG deposit in the Atacama Desert of northern Chile. Chlorine stable isotope data of atacamite vary between -0.62 and +2.1 ‰ and show a well-defined trend where δ37Cl values progressively decrease (become lighter) with depth. These data, when combined with new experimental determinations of chlorine isotope fractionation between atacamite and water, point to changes triggered by the progressive deepening of groundwater tables during Andean uplift and the extreme desiccation of

  5. Vol. 4 in the series: Site profiles of persistent chlorinated hydrocarbons - cause-oriented monitoring in aquatic media; Pestizide aus der Reihe der persistenten chlorierten Kohlenwasserstoffe in Gewaessern der Rhein-Region - Ergebnisse nachhaltiger Steuerungen von Wirtschaft und Politik. Bd. 4 der Reihe: Standortprofile persistenter chlorierter Kohlenwasserstoffe - ursachenorientiertes Monitoring in aquatischen Medien

    Energy Technology Data Exchange (ETDEWEB)

    Heinisch, E.; Kettrup, A.; Bergheim, W.; Wenzel, S.

    2003-07-01

    Evaluating the analytical data of DDT and its metabolites, the isomers of HCH as well as (sometimes) of aldrin and dieldrin in surface water, suspended matter, eels, breams and roaches from the rivers Rhine, Neckar, Kocher, Enz, Main (upto km 360), Weschnitz, Modau, Schwarzbach, Hengstbach, Grundbach, Nidda, Rodau, Kinzig, Werra, Diemel, Lahn, Nahe, Mosel, Sauer, Saar, Ahr, Kyll, Sieg and Laacher See distance profiles (partly from Konstanz till Markermeer) and time series (partly from 1984-2001) were elaborated. The primary data come from about 15 mainly regional investigation departments, the IKSR and the Environmental Specimen Bank. The chemical enterprises in Rheinfelden, Grenzach, Ludwigshafen, Lampertheim, Gernsheim, Darmstadt, Hoechst, Kelsterbach, Offenbach, Ingelheim, Loelsdorf, Leverkusen, Elberfeld, Krefeld-Uerdingen and Huels could partly be made transparent by the course of the sDDT and sHCH values and the profiles of the constituents and isomers, resp., in the distance profiles (especially from the river Rhine) mainly from 1990/92. The corresponding graph for the year 2000 shows that there is no longer a human and ecotoxicological relevance of the compounds to be expected. (orig.)

  6. Risk analysis associated with petroleum hydrocarbons: is everything running smoothly?

    International Nuclear Information System (INIS)

    Morin, D.

    1999-01-01

    Petroleum products represent one of the main sources of environmental contamination, and these products are complex, composed of several hundred individual hydrocarbons. The evaluation of the risks associated with petroleum products is often limited by certain specific parameters such as benzene. The petroleum hydrocarbons running from C(10) to C(50) are not often integrated in an analysis of the toxological risks since the toxological characterization of a complex mixture of hydrocarbons is difficult to carry out. There exist in the United States two approaches that were developed recently that allow the integration of various hydrocarbons comprising a mixture. In this presentation, two of these approaches are described and compared. An overview of these approaches related to Canadian regulatory bodies is included, and a case study completes the account. The two approaches that are most well known in this area are: 1) that of the Massachusetts Dept. of Environmental Protection, and 2) that of the Total Petroleum Hydrocarbon Criteria Working Group. The integration of petroleum hydrocarbons in a quantitative evaluation of their toxological risk is possible by present methods. This integration allows a reduction in the uncertainty associated with the use of an integrating parameter in the case of these petroleum hydrocarbons in the C(10) to the C(50) range

  7. Measuring Trace Hydrocarbons in Silanes

    Science.gov (United States)

    Lesser, L. A.

    1984-01-01

    Technique rapid and uses standard analytical equipment. Silane gas containing traces of hydrocarbons injected into carrier gas of moist nitrogen having about 0.2 percent water vapor. Carrier, water and silane pass through short column packed with powdered sodium hydroxide which combines moisture and silane to form nonvolatile sodium silicate. Carrier gas free of silane but containing nonreactive hydrocarbons, pass to silica-gel column where chromatographic separation takes place. Hydrocarbons measured by FID.

  8. UV/chlorine treatment of carbamazepine: Transformation products and their formation kinetics.

    Science.gov (United States)

    Pan, Yanheng; Cheng, ShuangShuang; Yang, Xin; Ren, Jingyue; Fang, Jingyun; Shang, Chii; Song, Weihua; Lian, Lushi; Zhang, Xinran

    2017-06-01

    Carbamazepine (CBZ) is one of the pharmaceuticals most frequently detected in the aqueous environment. This study investigated the transformation products when CBZ is degraded by chlorine under ultraviolet (UV) irradiation (the UV/chlorine process). Detailed pathways for the degradation of CBZ were elucidated using ultra-high performance liquid chromatography (UHPLC)-quadrupole time-of-flight mass spectrometry (QTOF-MS). CBZ is readily degraded by hydroxyl radicals (HO) and chlorine radicals (Cl) in the UV/chlorine process, and 24 transformation products were identified. The products indicate that the 10,11-double bond and aromatic ring in CBZ are the sites most susceptible to attack by HO and Cl. Subsequent reaction produces hydroxylated and chlorinated aromatic ring products. Four specific products were quantified and their evolution was related with the chlorine dose, pH, and natural organic matter concentration. Their yields showed an increase followed by a decreasing trend with prolonged reaction time. CBZ-10,11-epoxide (I), the main quantified transformation product from HO oxidation, was observed with a peak transformation yield of 3-32% depending on the conditions. The more toxic acridine (IV) was formed involving both HO and Cl with peak transformation yields of 0.4-1%. All four quantified products together amounted to a peak transformation yield of 34.5%. The potential toxicity of the transformation products was assayed by evaluating their inhibition of the bioluminescence of the bacterium Vibrio Fischeri. The inhibition increased at first and the decreased at longer reaction times, which was in parallel with the evolution of transformation products. Copyright © 2017 Elsevier Ltd. All rights reserved.

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

    Science.gov (United States)

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

    2007-08-01

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

  10. Transformation mechanism of benzophenone-4 in free chlorine promoted chlorination disinfection.

    Science.gov (United States)

    Xiao, Ming; Wei, Dongbin; Yin, Junxia; Wei, Guohua; Du, Yuguo

    2013-10-15

    The UV-filter BP-4 (2-hydroxy-4-methoxybenzophenone-5-sulfonic acid) has been frequently observed in the environment, showing high potentials to invade drinking water, swimming water, or wastewater reclamation treatment systems. With the help of high performance liquid chromatography-high resolution mass spectrometry and nuclear magnetic resonance spectroscopy, 10 new products from free chlorine-promoted BP-4 disinfection have been disclosed and their possible transformation routes have been investigated. The first route is chlorine substitution of BP-4 and its transformation products, forming mono-, di-, and tri-chlorinated BP-4 analogs. The second is Baeyer-Villiger-Type oxidation, converting diphenyl ketone to phenyl ester derivatives. The third is ester hydrolysis, generating corresponding phenolic and benzoic products. The fourth is decarboxylation, replacing the carboxyl group by chloride in the benzoic-type intermediate. The fifth is desulfonation, degrading the sulfonic group through an alternative chlorine substitution on the benzene ring. Orthogonal experiments have been established to investigate the species transformed from BP-4 at different pH values and free available chlorine (FAC) dosages. The reaction pathways are strongly dependent on pH conditions, while an excessive amount of FAC eliminates BP-4 to the smaller molecules. The initial transformation of BP-4 in chlorination system follows pseudo-first-order kinetics, and its half-lives ranged from 7.48 s to 1.26 × 10(2) s. More importantly, we have observed that the FAC-treated BP-4 aqueous solution might increase the genotoxic potentials due to the generation of chlorinated disinfection by-products. Copyright © 2013 Elsevier Ltd. All rights reserved.

  11. Antiradiation effectiveness of the chlorine C

    International Nuclear Information System (INIS)

    Bubnova, O.M.; Grechka, I.I.; Znamensky, V.V.

    1996-01-01

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

  12. Fractional separation of hydrocarbon vapours

    Energy Technology Data Exchange (ETDEWEB)

    1937-07-10

    A process is described for converting higher boiling hydrocarbons to lower boiling hydrocarbons by subjecting them at elevated temperatures to a conversion operation, then separating the higher and lower boiling fractions. The separation takes place while the reaction products are maintained in the vapor phase by contact with a mass of solid porous material which has little or no catalytic activity but does have a preferential absorption property for higher boiling hydrocarbons so that the lower boiling part of the reaction products pass through the separation zone while the heavier hydrocarbons are retained. The separation is accomplished without substantial loss of heat of these reaction products.

  13. A novel chlorine derivative of Meso-tris(pentafluorophenyl)-4-pyridyl porphyrin: synthesis, photophysics and photochemical properties

    Energy Technology Data Exchange (ETDEWEB)

    Maestrin, Ana Paula J.; Ribeiro, Anderson O.; Tedesco, Antonio Claudio; Neri, Claudio R.; Vinhado, Fabio S.; Serra, Osvaldo A.; Martins, Patricia R.; Iamamoto, Yassuko [Sao Paulo Univ., Ribeirao Preto, SP (Brazil). Faculdade de Filosofia, Ciencias e Letras. Inst. de Quimica]. E-mail: oaserra@ffclrp.usp.br; Silva, Ana Margarida G.; Tome, Augusto C.; Neves, Maria G.P.M.S.; Cavaleiro, Jose A.S. [Universidade de Aveiro (Portugal). Dept. de Quimica]. E-mail: jcavaleiro@dq.ua.pt

    2004-12-01

    Photodynamic therapy (PDT) is based on the accumulation of a photosensitizer, such as a porphyrin or a chlorine, in a malignant tissue after its administration. Chlorins exhibit photophysical properties similar to those of the porphyrin macrocycles, but with intensified and red-shifted Q bands, making chlorine-containing systems even better candidates for PDT. In this contribution, we report the synthesis of 5,10,15-tris(pentafluorophenyl)-20-(4-pyridyl)porphyrin, (2) and its transformation to the novel chlorine derivatives 4, (5,10,20-tris(pentafluorophenyl)-15-(4-pyridyl)-tetrahydro-1H- N-methyl-pyrrolo [3,4-b]porphyrin and 5, (5,10,15-tris(pentafluorophenyl)-20-(4-pyridyl)-tetrahydro-1H- N-methyl-pyrrolo[3,4-b]porphyrin) by 1,3-dipolar cycloaddition with an azomethine ylide. The new products have been characterized by UV-Vis, {sup 1}H NMR and FAB-MS. The photophysics, photochemical and photobleaching properties of chlorine 4 have been evaluated. Its quantum yield of photobleaching ({phi}{sub Pb}, mol Einstein{sup -1}) was 0.047{+-}0.014. In order to demonstrate the production of {sup 1}O{sub 2} when 4 is used as a photosensitizer, uric acid tests have been carried out. The results indicate that chlorine 4 can be considered a promising photosensitizer in PDT. (author)

  14. A novel chlorine derivative of Meso-tris(pentafluorophenyl)-4-pyridyl porphyrin: synthesis, photophysics and photochemical properties

    International Nuclear Information System (INIS)

    Maestrin, Ana Paula J.; Ribeiro, Anderson O.; Tedesco, Antonio Claudio; Neri, Claudio R.; Vinhado, Fabio S.; Serra, Osvaldo A.; Martins, Patricia R.; Iamamoto, Yassuko; Silva, Ana Margarida G.; Tome, Augusto C.; Neves, Maria G.P.M.S.; Cavaleiro, Jose A.S.

    2004-01-01

    Photodynamic therapy (PDT) is based on the accumulation of a photosensitizer, such as a porphyrin or a chlorine, in a malignant tissue after its administration. Chlorins exhibit photophysical properties similar to those of the porphyrin macrocycles, but with intensified and red-shifted Q bands, making chlorine-containing systems even better candidates for PDT. In this contribution, we report the synthesis of 5,10,15-tris(pentafluorophenyl)-20-(4-pyridyl)porphyrin, (2) and its transformation to the novel chlorine derivatives 4, (5,10,20-tris(pentafluorophenyl)-15-(4-pyridyl)-tetrahydro-1H- N-methyl-pyrrolo [3,4-b]porphyrin and 5, (5,10,15-tris(pentafluorophenyl)-20-(4-pyridyl)-tetrahydro-1H- N-methyl-pyrrolo[3,4-b]porphyrin) by 1,3-dipolar cycloaddition with an azomethine ylide. The new products have been characterized by UV-Vis, 1 H NMR and FAB-MS. The photophysics, photochemical and photobleaching properties of chlorine 4 have been evaluated. Its quantum yield of photobleaching (φ Pb , mol Einstein -1 ) was 0.047±0.014. In order to demonstrate the production of 1 O 2 when 4 is used as a photosensitizer, uric acid tests have been carried out. The results indicate that chlorine 4 can be considered a promising photosensitizer in PDT. (author)

  15. Multiresidue analysis of multiclass pesticides and polyaromatic hydrocarbons in fatty fish by gas chromatography tandem mass spectrometry and evaluation of matrix effect.

    Science.gov (United States)

    Chatterjee, Niladri S; Utture, Sagar; Banerjee, Kaushik; Ahammed Shabeer, T P; Kamble, Narayan; Mathew, Suseela; Ashok Kumar, K

    2016-04-01

    This paper reports a selective and sensitive method for multiresidue determination of 119 chemical residues including pesticides and polyaromatic hydrocarbons (PAH) in high fatty fish matrix. The novel sample preparation method involved extraction of the target analytes from homogenized fish meat (5 g) in acetonitrile (15 mL, 1% acetic acid) after three-phase partitioning with hexane (2 mL) and the remaining aqueous layer. An aliquot (1.5 mL) of the acetonitrile layer was aspirated and subjected to two-stage dispersive solid phase extraction (dSPE) cleanup and the residues were finally estimated by gas chromatography mass spectrometry with selected reaction monitoring (GC-MS/MS). The co-eluted matrix components were identified on the basis of their accurate mass by GC with quadrupole time of flight MS. Addition of hexane during extraction and optimized dSPE cleanup significantly minimized the matrix effects. Recoveries at 10, 25 and 50 μg/kg were within 60-120% with associated precision, RSD<11%. Copyright © 2015 Elsevier Ltd. All rights reserved.

  16. On the contribution of polycyclic aromatic hydrocarbons to the carcinogenic impact of automobile exhaust condensate evaluated by local application onto mouse skin.

    Science.gov (United States)

    Grimmer, G; Brune, H; Deutsch-Wenzel, R; Naujack, K W; Misfeld, J; Timm, J

    1983-11-01

    The objective of this investigation was to identify the substances chiefly responsible for the carcinogenicity of automobile exhaust condensate using topical application onto the skin of mice. This was performed by comparing the carcinogenic effect of various fractions with that of an unseparated sample of automobile exhaust condensate, tested in 3 different doses. The probit and Weibull analysis of the result shows: (a) The condensate, emitted from a gasoline-driven automobile provokes local tumors after long-term application to the dorsal skin of mice. The tumor incidence demonstrates a clear cut dose-response relationship. (b) The fraction of polycyclic aromatic hydrocarbons (PAH) containing more than 3 rings accounts for about 84-91% of the total carcinogenicity of automobile exhaust condensate. This fraction represents only about 3.5% by wt of the condensate. (c) The content of benzo[a]pyrene (BaP) (0.414 mg/g) accounts for 6-7.6% of the total carcinogenicity of automobile exhaust condensate, 15 selected PAHs for about 41%. (d) Regarding the minor effect of the PAH-free fraction (about 83% by wt), no hints for a cocarcinogenic activity were observed.

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

    International Nuclear Information System (INIS)

    Blondel, Antoine

    2013-01-01

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

  18. Process for preparing hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Krauch, C; Anther, E; Pier, M

    1926-04-07

    A process is described for the conversion of coal of all kinds, wood, oil, shale, as well as other carbonaceous materials into liquid hydrocarbons in two steps, characterized by treatment of the coal and so forth with a stream of hydrogen or hydrogen-containing gases at raised temperatures and raised pressures and producing a tarry product which, after separation of the ashlike residue, is converted by a further treatment, in the presence of catalysts, with hydrogen or hydrogen-containing gases at raised temperature and pressure, largely into low-boiling products.

  19. Recovering valuable liquid hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Pier, M

    1931-06-11

    A process for recovering valuable liquid hydrocarbons from coking coal, mineral coal, or oil shale through treatment with hydrogen under pressure at elevated temperature is described. Catalysts and grinding oil may be used in the process if necessary. The process provides for deashing the coal prior to hydrogenation and for preventing the coking and swelling of the deashed material. During the treatment with hydrogen, the coal is either mixed with coal low in bituminous material, such as lean coal or active coal, as a diluent or the bituminous constituents which cause the coking and swelling are removed by extraction with solvents. (BLM)

  20. Hydrogen production from hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Docekal, J

    1986-01-01

    Hydrogen is an important feed stock for chemical and petroleum industries, in addition to being considered as the energy carrier of the future. At the present time the feed stock hydrogen is mainly manufactured from hydrocarbons using steam reforming. In steam reforming two processes are employed, the conventional process and PSA (pressure swing adsorption) process. These two processes are described and compared. The results show that the total costs and the maintenance costs are lower for the PSA process, the capital outlay is lower for the conventional process, and the operating costs are similar for the two processes.

  1. Formation of chlorinated organic compounds in fluidized bed combustion of recycled fuels; Kloorattujen orgaanisten yhdisteiden muodostuminen kierraetyspolttoaineiden leijukerrospoltossa

    Energy Technology Data Exchange (ETDEWEB)

    Vesterinen, R.; Kallio, M.; Kirjalainen, T.; Kolsi, A.; Merta, M. [VTT Energy, Jyvaeskylae (Finland)

    1997-10-01

    Four tests of co-combustion of recycled fuels (REP) with peat and coal in the 15 kW fluidized bed reactor were performed. The recycled fuel was so-called dry fraction in four vessels sampling at Keltinmaeki. In three tests a part of peat energy was replaced with coal. The mixtures were prepared so that in all mixtures 25 % of energy was recycled fuel and 75 % was either peat or the mixture of peat and coal. The concentrations of polyaromatic hydrocarbons (PAH), polychlorinated dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs) and chlorophenols decreased with increasing part of coal due to the increasing sulphur/chlorine ratio. Principal Component Analysis (PCA) and Partial Least Square regression analysis (PLS) showed that the chlorine, copper and sulphur contents of the fuel effected most on the concentrations of chlorophenols, chlorobenzenes, PCBs and PCDDs/PCDFs. Other variables influencing on a model were the lead concentration and the sulphur/chlorine ratio in fuel and the hydrogen chloride concentration of the flue gas. The concentrations of chlorophenols and chlorobenzenes were also significant for PCDD/PCDF concentrations in flue gas. The sulphur, chlorine, copper and chromium contents in fly ash and the temperature of the reactor influenced on the chlorophenol, chlorobenzene, PCB and PCDD/PCDF concentrations in fly ash. The chlorophenol and chlorobenzene contents in fly ash, the sulphur/chlorine ratio and the lead content in fuel, the sulphur dioxide, hydrogen chloride and carbon monoxide concentrations in flue gas had also influence on PCDD/PCDF concentrations in fly ash

  2. Dispersion of chlorine at seven southern California coastal generating stations

    International Nuclear Information System (INIS)

    Grove, R.S.

    1983-01-01

    The objectives of this study were to (1) determine chlorine concentrations and exposure time gradients of chlorine through seven coastal generating stations and (2) assess the dispersion characteristics of chlorine in the receiving waters. Remarkable variability in chlorine injection concentrations, condenser outlet concentrations, outfall concentrations, and dissipation rates between generating stations and, to a lesser extent, between surveys at the same generating station was found in this chlorine monitoring study. Other than quite consistent low injection and correspondingly low outfall concentrations at San Onofre (a generating station that had one of the more rigorous chlorine control and minimization programs in effect at the time), no recognizable patterns of chlorination could be discerned in the data. Over half of the outfall chlorine surveys had chlorine concentrations below 0.08 mg/L, which is the accepted level of detection for the titrator being used in the surveys. The post-outfall dilution calculations further showed that the chlorine that does enter the receiving water is initially diluted with entrained ambient water at a ratio of 5.2:19.0

  3. Spectrographic determination of chlorine and fluorine

    International Nuclear Information System (INIS)

    Contamin, G.

    1965-04-01

    Experimental conditions have been investigated in order to obtain the highest sensitivity in spectrographic determination of chlorine and fluorine using the Fassel method of excitation in an inert atmosphere. The influence of the nature of the atmosphere, of the discharge conditions and of the matrix material has been investigated. The following results have been established: 1. chlorine determination is definitely possible: a working curve has been drawn between 10 μg and 100 μg, the detection limit being around 5 μg; 2. fluorine determination is not satisfactory: the detection limit is still of the order of 80 μg. The best operating conditions have been defined for both elements. (author) [fr

  4. Chlorine-36 dating of continental evaporites

    International Nuclear Information System (INIS)

    Huang Qi

    1990-01-01

    Teh chloring-36 production, principle and experimental method of 36 Cl dating are briefly described. The ages calculated from the 36 Cl/Cl ratios are generally concordant with those obtained by using 14 C, 230 Th and magnetostratigraphic techniques. It confirms the constancy of the chlorine input ratio over the last million years and implys that 36 Cl can provide accurate dates on continental saline sediments

  5. Thermal diffusion of chlorine in uranium dioxide

    International Nuclear Information System (INIS)

    Pipon, Y.; Toulhoat, N.; Moncoffre, N.; Jaffrezic, H.; Gavarini, S.; Martin, P.; Raimbault, L.; Scheidegger, A.M.

    2006-01-01

    In a nuclear reactor, isotopes such as 35 Cl present as impurities in the nuclear fuel are activated by thermal neutron capture. During interim storage or geological disposal of nuclear fuel, the activation products such as 36 Cl may be released from the fuel to the geo/biosphere and contribute to the ''instant release fraction'' as they are likely to migrate in defects and grain boundaries. In order to differentiate diffusion mechanisms due to ''athermal'' processes during irradiation from thermally activated diffusion, both irradiation and thermal effects must be assessed. This work concerns the measurement of the thermal diffusion coefficient of chlorine in UO 2 . 37 Cl was implanted at a 10 13 at/cm 2 fluence in depleted UO 2 samples which were then annealed in the 900-1200 C temperature range and finally analyzed by secondary ion mass spectrometry (SIMS) to obtain 37 Cl depth profiles. The migration process appears to be rather complex, involving mechanisms such as atomic, grain boundary, directed diffusion along preferential patterns as well as trapping into sinks before successive effusion. However, using a diffusion model based on general equation of transport, apparent diffusion coefficients could be calculated for 1000 and 1100 C and a mean activation energy of 4.3 eV is proposed. This value is one of the lowest values compared to those found in literature for other radionuclides pointing out a great ability of chlorine to migrate in UO 2 at relatively low temperatures. In order to unequivocally determine the diffusion behaviour of both implanted and pristine chlorine before and after thermal annealing, the structural environment of chlorine in UO 2 was examined using micro X-ray fluorescence (micro-XRF) and micro X-ray absorption spectroscopy (micro-XAS). (orig.)

  6. Accumulation of chlorinated benzenes in earthworms

    Science.gov (United States)

    Beyer, W.N.

    1996-01-01

    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. This paper describes a long-term (26 week) experiment relating the concentrations of chlorinated benzenes in earthworms to 1) the length of exposure, and it describes three 8-week experiments relating concentrations of chlorinated benzenes in earthworms to 2) their concentration in soil 3) the soil organic matter content and, 4) the degree of chlorination. In the 26-week experiment, the concentration of 1,2,4 - trichlorobenzene in earthworms fluctuated only slightly about a mean of 0.63 ppm (Fig. 1). Although a statistically significant decrease can be demonstrated over the test (Pearson correlation coefficient, r = -0.62 p earthworms showed a cyclical trend that coincided with replacement of the media, and a slight but statistically significant tendency to increase from about 2 to 3 ppm over the 26 weeks (r = 0.55, p earthworms increased as the concentrations in the soil increased (Fig. 2), but leveled off at the highest soil concentrations. The most surprising result of this study was the relatively low concentrations in earthworms compared to those in soils. The average concentration of each of the six isomers of trichlorobenzene and tetrachlorobenzene in earthworms was only about 1 ppm (Table 2); the isomeric structure did not affect accumulation. The concentration of organic matter in soil had a prominent effect on hexachlorobenzene concentrations in earthworms (Fig. 3). Hexachlorobenzene concentrations decreased steadily from 9.3 ppm in earthworms kept in soil without any peat moss added to about 1 ppm in soil containing 16 or 32% organic matter.

  7. Determination of polynuclear hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Lodge, Jr, J P

    1963-01-01

    At the present time, the method of choice for the determination of polynuclear hydrocarbons appears to be the following, (a) extraction of the benzene-soluble fraction from the gross collected particulate matter, (b) one pass through a chromatographic column of partially deactivated alumina, (c) spectral examination of the fractions and (d) the application of appropriate chemical tests as indicated by the previous step. Using this method, the presence of pyrene, fluoranthene, one of the benzofluorenes, chrysens, benz(a)anthracene, benzo(a)pyrene, benzo(e)pyrene, benzo(k)fluoranthene, anthanthrene, and coronene was demonstrated in the air of numerous American cities, and benzo(a)pyrene was measured at some 130 sites. Invaluable as such accurate determinations may be for research purposes, they are still too costly and time-consuming for routine survey purposes. While studies on the subject are by no means complete, they indicate the validity of piperonal chloride test as a general index of polycyclic hydrocarbons. This procedure is described in this paper. 7 references.

  8. Hydrocarbons: source of energy

    International Nuclear Information System (INIS)

    Imarisio, G.; Frias, M.; Bemtgen, J.M.

    1989-01-01

    Hydrocarbons are at present the single most important source of energy, since they are the most versatile and widely used. It is expected that their importance will extend well into the next century and therefore it is essential to provide for all those improvements which will extend their availability and usefulness. The sub-programme ''Optimization of the production and utilization of hydrocarbons'' (within the Non-Nuclear Energy R and D Programme of the European Communities) is pursuing a number of R and D topics aimed at the above-mentioned results. It is implemented by means of shared-cost R and D contracts. At this first Seminar held in Lyon (France) from 21-23 September, 1988, all contractors of the sub-programme presented the state of progress of their R and D projects. These proceedings comprise all the papers presented at the Seminar. The section on oilfield exploration includes a report of work on the interpretation of nuclear logs by means of mathematical models. (author)

  9. Chlorination and Carbochlorination of Cerium Oxide

    International Nuclear Information System (INIS)

    Esquivel, Marcelo; Bohe, Ana; Pasquevich, Daniel

    2000-01-01

    The chlorination and carbochlorination of cerium oxide were studied by thermogravimetry under controlled atmosphere (TG) in the 700 0 C 950 0 C temperature range.Both reactants and products were analyzed by X-ray diffraction (RX), scanning electronic microscopy (SEM) and energy dispersive spectroscopy (EDS). Thermodynamic calculations were performed by computer assisted software.The chlorination starts at a temperature close to 800 0 C.This reaction involves the simultaneous formation and evaporation of CeCl3.Both processes control the reaction rate and their kinetic may not be easily separated.The apparent chlorination activation energy in the 850 0 C-950 0 C temperature range is 172 to 5 kJ/ mole.Carbon transforms the CeO2-Cl2 into a more reactive system: CeO2-C-Cl2, where the effects of the carbon content, total flow rate and temperature were analyzed.The carbochlorination starting temperature is 700 0 C.This reaction is completed in one step controlled by mass transfer with an apparent activation energy of 56 to 5 kJ/mole in the 850 0 C-950 0 C temperature range

  10. Radioimmunoassay for chlorinated dibenzo-p-dioxins

    International Nuclear Information System (INIS)

    Albro, P.W.; Chae, K.; Luster, M.I.; Mckinney, J.D.

    1980-01-01

    The invention provides a double-antibody radioimmunoassay method for the determination of chlorinated dibenzo-p-dioxins, particularly, 2,3,7,8-tetrachlorodibenzo-p-dioxin, in environmental samples including animal tissues such as monkey liver and adipose tissues. The limit of detection is approximately 25 picograms for 2,3,7,8-tetrachlorodibenzo-pdioxin. Assuming an appropriate cleanup procedure is used, chlorinated dibenzofurans are the only likely interferences, and these can be distinguished through the use of two antisers of different dibenzo-furan/dibenzodioxin selectivities. The invention includes the preparation of a reproducible antigen, an appropriate radiolabeled hapten, and effective sample extracts. A feature of the assay method is the use of a nonionic detergent (e.g., ''cutscum'' or ''triton x-305'') to solubilize the extremely hydrophobic dibenzo-p-dioxins in a manner permitting their binding by antibodies. The immunoassay is applicable to screening samples in order to minimize the demand for mass spectrometric screening, and to routine monitoring for exposure to known chlorinated dibenzo-p-dioxins in potentially contaminated environments

  11. Concentration and Risk Evaluation of Polycyclic Aromatic Hydrocarbons in Urban Soil in the Typical Semi-Arid City of Xi’an in Northwest China

    Directory of Open Access Journals (Sweden)

    Lijun Wang

    2018-03-01

    Full Text Available Polycyclic aromatic hydrocarbons (PAHs are ubiquitous environmental pollutants, presenting potential threats to the ecological environment and human health. Sixty-two urban soil samples were collected in the typical semi-arid city of Xi’an in Northwest China. They were analyzed for concentration, pollution, and ecological and health risk of sixteen U.S. Environmental Protection Agency priority PAHs. The total concentrations of the sixteen PAHs (Σ16PAHs in the urban soil ranged from 390.6 to 10,652.8 µg/kg with an average of 2052.6 µg/kg. The concentrations of some individual PAHs in the urban soil exceeded Dutch Target Values of Soil Quality and the Σ16PAHs represented heavy pollution. Pyrene and dibenz[a,h]anthracene had high ecological risk to aquatic/soil organisms, while other individual PAHs showed low ecological risk. The total ecological risk of PAHs to aquatic/soil organisms is classified as moderate. Toxic equivalency quantities (TEQs of the sixteen PAHs varied between 21.16 and 1625.78 µg/kg, with an average of 423.86 µg/kg, indicating a relatively high toxicity potential. Ingestion and dermal adsorption of soil dust were major pathways of human exposure to PAHs from urban soil. Incremental lifetime cancer risks (ILCRs of human exposure to PAHs were 2.86 × 10−5 for children and 2.53 × 10−5 for adults, suggesting that the cancer risk of human exposure to PAHs from urban soil is acceptable.

  12. Concentration and Risk Evaluation of Polycyclic Aromatic Hydrocarbons in Urban Soil in the Typical Semi-Arid City of Xi’an in Northwest China

    Science.gov (United States)

    Wang, Lijun; Zhang, Shengwei; Wang, Li; Zhang, Wenjuan; Shi, Xingmin; Lu, Xinwei; Li, Xiaoping; Li, Xiaoyun

    2018-01-01

    Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous environmental pollutants, presenting potential threats to the ecological environment and human health. Sixty-two urban soil samples were collected in the typical semi-arid city of Xi’an in Northwest China. They were analyzed for concentration, pollution, and ecological and health risk of sixteen U.S. Environmental Protection Agency priority PAHs. The total concentrations of the sixteen PAHs (Σ16PAHs) in the urban soil ranged from 390.6 to 10,652.8 µg/kg with an average of 2052.6 µg/kg. The concentrations of some individual PAHs in the urban soil exceeded Dutch Target Values of Soil Quality and the Σ16PAHs represented heavy pollution. Pyrene and dibenz[a,h]anthracene had high ecological risk to aquatic/soil organisms, while other individual PAHs showed low ecological risk. The total ecological risk of PAHs to aquatic/soil organisms is classified as moderate. Toxic equivalency quantities (TEQs) of the sixteen PAHs varied between 21.16 and 1625.78 µg/kg, with an average of 423.86 µg/kg, indicating a relatively high toxicity potential. Ingestion and dermal adsorption of soil dust were major pathways of human exposure to PAHs from urban soil. Incremental lifetime cancer risks (ILCRs) of human exposure to PAHs were 2.86 × 10−5 for children and 2.53 × 10−5 for adults, suggesting that the cancer risk of human exposure to PAHs from urban soil is acceptable. PMID:29584654

  13. Structural segregation of petroleum and prospective hydrocarbon regions in Azerbaijan

    International Nuclear Information System (INIS)

    Kerimov, K.M.; Huseynov, A.N.; Hajiyev, F.M.

    2002-01-01

    Full text : Structural segregation allows identify the earth crust blocks according to their geological setting and structural history conductive for hydrocarbon generation and their entrapment in the sedimentary fill reservoirs. Since then there has been a need to design a new tectonic map of petroleum and hydrocarbons potential systems in Azerbaijan embracing both on- and offshore areas. Map's legend designed upon above mentioned concepts and principles has made it possible to evaluate the role of individual stratigraphic units in hydrocarbon generation and its entrapment, as well as in recognition of regional structural criteria of the hydrocarbon bearing potential of different structural patterns. Tectonic map of petroleum and prospective hydrocarbon bearing on and offshore areas in Azerbaijan for the first time contained a wide range of information related to structural criteria of hydrocarbon bearing potential, sedimentary fill's structural architecture, its thickness, both timing of their formation stages and basement consolidation, its subsidence depth, as well as hydrocarbon deposit areal and vertical distribution across individual regions. This map was considered to be of important implication both for the petroleum geoscience and petroleum industry endeavors.

  14. Identification of intermediates leading to chloroform and C-4 diacids in the chlorination of humic acid

    NARCIS (Netherlands)

    Sinninghe Damsté, J.S.; Leer, E.W.B. de; Erkelens, Corrie; Galan, L.

    1985-01-01

    The chlorination of terrestrial humic acid was studied at pH 7. 2 with varying chlorine to carbon ratios. The principal products are chloroform, di- and trichloroacetic acid, and chlorinated C-4 diacids. At a high chlorine dose many new chlorination products were detected, among them

  15. Degradation of Chlorinated Aliphatic Hydrocarbons by Methylosinus trichosporium OB3b Expressing Soluble Methane Monooxygenase

    NARCIS (Netherlands)

    Oldenhuis, R.; Vink, Ruud L.J.M.; Janssen, D. B.; Witholt, B.

    1989-01-01

    Degradation of trichloroethylene (TCE) by the methanotrophic bacterium Methylosinus trichosporium OB3b was studied by using cells grown in continuous culture. TCE degradation was a strictly cometabolic process, requiring the presence of a cosubstrate, preferably formate, and oxygen. M. trichosporium

  16. Effect of solvent alcohol on degradation of chlorinated hydrocarbons by γ-irradiation

    International Nuclear Information System (INIS)

    Nakagawa, Seiko

    2002-01-01

    1,1,2-Trichloro-trifluoroethane (CFC113) was dissolved in alkaline 1-butanol, 2-butanol, iso-butyl alcohol, and phenyl ethyl alcohol and irradiated with 60 Co gamma rays after being purged with pure nitrogen gas. In all these solvents, the concentration of CFC113 and hydroxide ion decreased and that of chloride ion increased with a dose observed in 2-propanol solution. The reaction efficiency increases in the following order: 1-butanol < iso-butyl alcohol < phenyl ethyl alcohol < 2-butanol < 2-propanol. The solvent effect will depend on the binding energy of the αC-H of the alcohol molecule and