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Sample records for aromatic hydrocarbon degradation

  1. Microbial Degradation of Polycyclic Aromatic Hydrocarbons and Characterization of Bacteria

    Science.gov (United States)

    Tikilili, P. V.; Chirwa, E. M. N.

    2010-01-01

    Biodegradation of polycyclic aromatic hydrocarbons was studied. Naphthalene was used as a model compound to represent these compounds. Low initial concentrations of naphthalene in a range of 30-60 mg/L were completely degraded after incubation for 15 hrs by consortia from a landfill soil while consortia from minewater took more that 29 hrs to reach complete degradation.

  2. Degradation of polynuclear aromatic hydrocarbons by two strains of Pseudomonas.

    Science.gov (United States)

    Nwinyi, Obinna C; Ajayi, Oluseyi O; Amund, Olukayode O

    2016-01-01

    The goal of this investigation was to isolate competent polynuclear aromatic hydrocarbons degraders that can utilize polynuclear aromatic hydrocarbons of former industrial sites at McDoel Switchyard in Bloomington, Indiana. Using conventional enrichment method based on soil slurry, we isolated, screened and purified two bacterial species strains PB1 and PB2. Applying the ribotyping technique using the 16S rRNA gene analysis, the strains were assigned to the genus Pseudomonas (Pseudomonas plecoglossicida strain PB1 and Pseudomonas sp. PB2). Both isolates showed promising metabolic capacity on pyrene sprayed MS agar plates during the preliminary investigations. Using time course studies in the liquid cultures at calculated concentrations 123, 64, 97 and 94ppm for naphthalene, chrysene, fluroanthene and pyrene, P. plecoglossicida strain PB1 and Pseudomonas sp. PB2 showed partial utilization of the polynuclear aromatic hydrocarbons. Naphthalene was degraded between 26% and 40%, chrysene 14% and 16%, fluroanthene 5% and 7%; pyrene 8% and 13% by P. plecoglossicida strain PB1 and Pseudomonas sp. PB2 respectively. Based on their growth profile, we developed a model R(2)=1 to predict the degradation rate of slow polynuclear aromatic hydrocarbon-degraders where all the necessary parameters are constant. From this investigation, we confirm that the former industrial site soil microbial communities may be explored for the biorestoration of the industrial site. PMID:27245129

  3. Occurrence of fungi degrading aromatic hydrocarbons in activated sludge biocenoses

    Directory of Open Access Journals (Sweden)

    Anna Grabińska-Łoniewska

    2014-08-01

    Full Text Available A set of 21 strains of yeast-like microorganisms isolated from biocenoses of aerobic and anaerobic wastewater treatment systems were assayed for their ability to utilize aromatic hydrocarbons as a sole C-source. Basing on the achieved results, the highly biochemically active strains for application in enhancing of wastewaters and exhaust gases purification as well as soil bioremediation were selected.

  4. Aromatic Hydrocarbons: Degrading Bacteria in the Desert Soil of Kuwait

    International Nuclear Information System (INIS)

    Soil samples of different levels of oil pollutants were collected from Kuwait's Burgan Oil Field, near an oil lake. The samples represented, highly polluted (8.0% w/w), moderately polluted (2.1%-3.4%) and slightly polluted (2.1%-3.4%) and slightly polluted (0.5- 0.8%). The aromatic fractions of the collected samples were in the range of (0.21-2.57g/100g) soil. (GC) analysis of the aromatic fractions of the resolution of the different individual (PAHs) revealed the presence of (16) different (PAHs) resolved from the aromatic fraction of the highly polluted sample (S3). (15), (14) and (13) individual (PAHs) were identified soil samples (S5), (S2) and (S1, S4, S6) respectively. The most frequent (PAH) was indeno (1, 2, 3-c, d) pyrene (22.5%-45.11%) followed chrysene (13.6%-19.48%). Eight carcinogenic (PAHs) were resolved from the aromatic fractions of the polluted samples. Total carcinogenic (PAHs) recorded in this study were in this study were in the range of (11.53) (forS4) - (510.98) (for S3) ppm. The counts of (CFU) of aromatic degraders (AD) were in the range of (3x10) - (110x 10) (CFU/g) soil (with a percent of (2.2%-69.6%)). The results show that, higher counts of (AD) were recorded from a highly polluted sample (S3), followed by the moderately polluted samples; total of (51) bacteria, that gave presumptive positive biodegradation activities, were isolated and identified (45.1%) of them were isolated and identified. (45.1%) of them were isolated from the highly polluted sample (S3). Total of (13) different species were identified of which Micrococcus luteus was more frequent (23.5) followed by Bacillus licheniformis (19.6%) and Bacillus subtilis (11.8%). The three Pseudomonas species collectively were presented by (11.8%). Five different species proved to be of good activities, they are: Bacillus brevis, Bacillus lichenoformis, Pseudomonas aeruginosa, Pseudomonas stutzeri and Pseudomonas flourescens. The ability of five species and their mixture was

  5. Enumeration and phylogenetic analysis of polycyclic aromatic hydrocarbon-degrading marine bacteria from Puget sound sediments.

    OpenAIRE

    Geiselbrecht, A D; Herwig, R P; Deming, J. W.; Staley, J T

    1996-01-01

    Naphthalene- and phenanthrene-degrading bacteria in Puget Sound sediments were enumerated by most-probable-number enumeration procedures. Sediments from a creosote-contaminated Environmental Protection Agency Superfund Site (Eagle Harbor) contained from 10(4) to 10(7) polycyclic aromatic hydrocarbon (PAH)-degrading bacteria g (dry weight) of sediment-1, whereas the concentration at an uncontaminated site ranged from 10(3) to 10(4) g of sediment(-1). Isolates of PAH-degrading bacteria were obt...

  6. Polycyclic Aromatic Hydrocarbon Degradation by a New Marine Bacterium, Neptunomonas naphthovorans gen. nov., sp. nov.

    OpenAIRE

    Hedlund, Brian P.; Geiselbrecht, Allison D.; Bair, Timothy J.; Staley, James T.

    1999-01-01

    Two strains of bacteria were isolated from creosote-contaminated Puget Sound sediment based on their ability to utilize naphthalene as a sole carbon and energy source. When incubated with a polycyclic aromatic hydrocarbon (PAH) compound in artificial seawater, each strain also degraded 2-methylnaphthalene and 1-methylnaphthalene; in addition, one strain, NAG-2N-113, degraded 2,6-dimethylnaphthalene and phenanthrene. Acenaphthene was not degraded when it was used as a sole carbon source but wa...

  7. Degradation of benzene and other aromatic hydrocarbons by anaerobic bacteria

    NARCIS (Netherlands)

    Weelink, S.A.B.

    2008-01-01

    Accidental spills, industrial discharges and gasoline leakage from underground storage tanks have resulted in serious pollution of the environment with monoaromatic hydrocarbons, such as benzene, toluene, ethylbenzene and xylene (so-called BTEX). High concentrations of BTEX have been detected in soi

  8. Degradation of benzene and other aromatic hydrocarbons by anaerobic bacteria

    OpenAIRE

    Weelink, S.A.B.

    2008-01-01

    Accidental spills, industrial discharges and gasoline leakage from underground storage tanks have resulted in serious pollution of the environment with monoaromatic hydrocarbons, such as benzene, toluene, ethylbenzene and xylene (so-called BTEX). High concentrations of BTEX have been detected in soils, sediments and groundwater. The mobility and toxicity of the BTEX compounds are of major concern. In situ bioremediation of BTEX by using naturally occurring microorganisms or introduced microor...

  9. Variability of Biological Degradation of Aromatic Hydrocarbons in an Aerobic Aquifer Determined by Laboratory Batch Experiments

    DEFF Research Database (Denmark)

    Nielsen, Per Henning; Christensen, Thomas Højlund

    1994-01-01

    The biological aerobic degradation of 7 aromatic hydrocarbons (benzene, toluene, o-xylene, p-dichlorobenzene, o-dichlorobenzene, naphthalene and biphenyl) was studied for 149 days in replicate laboratory batch experiments with groundwater and sediment from 8 localities representing a 15 m × 30 m...... section of an aerobic aquifer. Compared to biologically deactivated control experiments all compounds were biologically degraded. Degradation curves were very reproducible for some compounds (benzene, toluene, o-xylene, o-dichlorobenzene and p-dichlorobenzene) and less reproducible for other (naphthalene...... and biphenyl). Based on observed length of lag phases, length of the degradation periods and percent degradation, the variation among the 8 localities appears to be modest. However, detailed examination of the degradation rates revealed statistically significant variation among localities for benzene, toluene...

  10. Microbial degradation of street dust polycyclic aromatic hydrocarbons in microcosms simulating diffuse pollution of urban soil

    DEFF Research Database (Denmark)

    Johnsen, Anders R; de Lipthay, Julia R; Sørensen, Søren J;

    2006-01-01

    Diffuse pollution with polycyclic aromatic hydrocarbons (PAHs) of topsoil in urban regions has caused increasing concerns in recent years. We simulated diffuse pollution of soil in microcosms by spiking sandy topsoil (A-horizon) and coarse, mineral subsoil (C-horizon) with street dust (PM63......) isolated from municipal street sweepings from central Copenhagen. The microbial communities adapted to PAH degradation in microcosms spiked with street dust in both A-horizon and C-horizon soils, in spite of low PAH-concentrations. The increased potential for PAH degradation was demonstrated on several...... levels: by slowly diminishing PAH-concentrations, increased mineralization of 14C-PAHs, increasing numbers of PAH degraders and increased prevalence of nah and pdo1 PAH degradation genes, i.e. the microbial communities quickly adapted to PAH degradation. Three- and 4-ring PAHs from the street dust were...

  11. Functional Gene Markers for Fumarate-Adding and Dearomatizing Key Enzymes in Anaerobic Aromatic Hydrocarbon Degradation in Terrestrial Environments.

    Science.gov (United States)

    von Netzer, Frederick; Kuntze, Kevin; Vogt, Carsten; Richnow, Hans H; Boll, Matthias; Lueders, Tillmann

    2016-01-01

    Anaerobic degradation is a key process in many environments either naturally or anthropogenically exposed to petroleum hydrocarbons. Considerable advances into the biochemistry and physiology of selected anaerobic degraders have been achieved over the last decades, especially for the degradation of aromatic hydrocarbons. However, researchers have only recently begun to explore the ecology of complex anaerobic hydrocarbon degrader communities directly in their natural habitats, as well as in complex laboratory systems using tools of molecular biology. These approaches have mainly been facilitated by the establishment of a suite of targeted marker gene assays, allowing for rapid and directed insights into the diversity as well as the identity of intrinsic degrader populations and degradation potentials established at hydrocarbon-impacted sites. These are based on genes encoding either peripheral or central key enzymes in aromatic compound breakdown, such as fumarate-adding benzylsuccinate synthases or dearomatizing aryl-coenzyme A reductases, or on aromatic ring-cleaving hydrolases. Here, we review recent advances in this field, explain the different detection methodologies applied, and discuss how the detection of site-specific catabolic gene markers has improved the understanding of processes at contaminated sites. Functional marker gene-based strategies may be vital for the development of a more elaborate population-based assessment and prediction of aromatic degradation potentials in hydrocarbon-impacted environments. PMID:26959523

  12. Reconstruction of metabolic networks in a fluoranthene-degrading enrichments from polycyclic aromatic hydrocarbon polluted soil.

    Science.gov (United States)

    Zhao, Jian-Kang; Li, Xiao-Ming; Ai, Guo-Min; Deng, Ye; Liu, Shuang-Jiang; Jiang, Cheng-Ying

    2016-11-15

    Microbial degradation of polycyclic aromatic hydrocarbons (PAHs) is the primary process of removing PAHs from environments. The metabolic pathway of PAHs in pure cultures has been intensively studied, but cooperative metabolisms at community-level remained to be explored. In this study, we determined the dynamic composition of a microbial community and its metabolic intermediates during fluoranthene degradation using high-throughput metagenomics and gas chromatography-mass spectrometry (GC-MS), respectively. Subsequently, a cooperative metabolic network for fluoranthene degradation was constructed. The network shows that Mycobacterium contributed the majority of ring-hydroxylating and -cleavage dioxygenases, while Diaphorobacter contributed most of the dehydrogenases. Hyphomicrobium, Agrobacterium, and Sphingopyxis contributed to genes encoding enzymes involved in downstream reactions of fluoranthene degradation. The contributions of various microbial groups were calculated with the PICRUSt program. The contributions of Hyphomicrobium to alcohol dehydrogenases were 62.4% in stage 1 (i.e., when fluoranthene was rapidly removed) and 76.8% in stage 3 (i.e., when fluoranthene was not detectable), respectively; the contribution of Pseudomonas were 6.6% in stage 1 and decreased to 1.2% in subsequent stages. To the best of the author's knowledge, this report describes the first cooperative metabolic network to predict the contributions of various microbial groups during PAH-degradation at community-level. PMID:27415596

  13. Proteogenomic Characterization of Monocyclic Aromatic Hydrocarbon Degradation Pathways in the Aniline-Degrading Bacterium Burkholderia sp. K24.

    Directory of Open Access Journals (Sweden)

    Sang-Yeop Lee

    Full Text Available Burkholderia sp. K24, formerly known as Acinetobacter lwoffii K24, is a soil bacterium capable of utilizing aniline as its sole carbon and nitrogen source. Genomic sequence analysis revealed that this bacterium possesses putative gene clusters for biodegradation of various monocyclic aromatic hydrocarbons (MAHs, including benzene, toluene, and xylene (BTX, as well as aniline. We verified the proposed MAH biodegradation pathways by dioxygenase activity assays, RT-PCR, and LC/MS-based quantitative proteomic analyses. This proteogenomic approach revealed four independent degradation pathways, all converging into the citric acid cycle. Aniline and p-hydroxybenzoate degradation pathways converged into the β-ketoadipate pathway. Benzoate and toluene were degraded through the benzoyl-CoA degradation pathway. The xylene isomers, i.e., o-, m-, and p-xylene, were degraded via the extradiol cleavage pathways. Salicylate was degraded through the gentisate degradation pathway. Our results show that Burkholderia sp. K24 possesses versatile biodegradation pathways, which may be employed for efficient bioremediation of aniline and BTX.

  14. Microbial degradation of street dust polycyclic aromatic hydrocarbons in microcosms simulating diffuse pollution of urban soil.

    Science.gov (United States)

    Johnsen, Anders R; de Lipthay, Julia R; Sørensen, Søren J; Ekelund, Flemming; Christensen, Peter; Andersen, Ole; Karlson, Ulrich; Jacobsen, Carsten S

    2006-03-01

    Diffuse pollution with polycyclic aromatic hydrocarbons (PAHs) of topsoil in urban regions has caused increasing concerns in recent years. We simulated diffuse pollution of soil in microcosms by spiking sandy topsoil (A-horizon) and coarse, mineral subsoil (C-horizon) with street dust (PM63) isolated from municipal street sweepings from central Copenhagen. The microbial communities adapted to PAH degradation in microcosms spiked with street dust in both A-horizon and C-horizon soils, in spite of low PAH-concentrations. The increased potential for PAH degradation was demonstrated on several levels: by slowly diminishing PAH-concentrations, increased mineralization of 14C-PAHs, increasing numbers of PAH degraders and increased prevalence of nah and pdo1 PAH degradation genes, i.e. the microbial communities quickly adapted to PAH degradation. Three- and 4-ring PAHs from the street dust were biodegraded to some extent (10-20%), but 5- and 6-ring PAHs were not biodegraded in spite of frequent soil mixing and high PAH degradation potentials. In addition to biodegradation, leaching of 2-, 3- and 4-ring PAHs from the A-horizon to the C-horizon seems to reduce PAH-levels in surface soil. Over time, levels of 2-, 3- and 4-ring PAHs in surface soil may reach equilibrium between input and the combination of biodegradation and leaching. However, levels of the environmentally critical 5- and 6-ring PAHs will probably continue to rise. We presume that sorption to black carbon particles is responsible for the persistence and low bioaccessibility of 5- and 6-ring PAHs in diffusely polluted soil.

  15. Current State of Knowledge in Microbial Degradation of Polycyclic Aromatic Hydrocarbons (PAHs): A Review

    Science.gov (United States)

    Ghosal, Debajyoti; Ghosh, Shreya; Dutta, Tapan K.; Ahn, Youngho

    2016-01-01

    Polycyclic aromatic hydrocarbons (PAHs) include a group of organic priority pollutants of critical environmental and public health concern due to their toxic, genotoxic, mutagenic and/or carcinogenic properties and their ubiquitous occurrence as well as recalcitrance. The increased awareness of their various adverse effects on ecosystem and human health has led to a dramatic increase in research aimed toward removing PAHs from the environment. PAHs may undergo adsorption, volatilization, photolysis, and chemical oxidation, although transformation by microorganisms is the major neutralization process of PAH-contaminated sites in an ecologically accepted manner. Microbial degradation of PAHs depends on various environmental conditions, such as nutrients, number and kind of the microorganisms, nature as well as chemical property of the PAH being degraded. A wide variety of bacterial, fungal and algal species have the potential to degrade/transform PAHs, among which bacteria and fungi mediated degradation has been studied most extensively. In last few decades microbial community analysis, biochemical pathway for PAHs degradation, gene organization, enzyme system, genetic regulation for PAH degradation have been explored in great detail. Although, xenobiotic-degrading microorganisms have incredible potential to restore contaminated environments inexpensively yet effectively, but new advancements are required to make such microbes effective and more powerful in removing those compounds, which were once thought to be recalcitrant. Recent analytical chemistry and genetic engineering tools might help to improve the efficiency of degradation of PAHs by microorganisms, and minimize uncertainties of successful bioremediation. However, appropriate implementation of the potential of naturally occurring microorganisms for field bioremediation could be considerably enhanced by optimizing certain factors such as bioavailability, adsorption and mass transfer of PAHs. The main

  16. Current State of Knowledge in Microbial Degradation of Polycyclic Aromatic Hydrocarbons (PAHs): A Review.

    Science.gov (United States)

    Ghosal, Debajyoti; Ghosh, Shreya; Dutta, Tapan K; Ahn, Youngho

    2016-01-01

    Polycyclic aromatic hydrocarbons (PAHs) include a group of organic priority pollutants of critical environmental and public health concern due to their toxic, genotoxic, mutagenic and/or carcinogenic properties and their ubiquitous occurrence as well as recalcitrance. The increased awareness of their various adverse effects on ecosystem and human health has led to a dramatic increase in research aimed toward removing PAHs from the environment. PAHs may undergo adsorption, volatilization, photolysis, and chemical oxidation, although transformation by microorganisms is the major neutralization process of PAH-contaminated sites in an ecologically accepted manner. Microbial degradation of PAHs depends on various environmental conditions, such as nutrients, number and kind of the microorganisms, nature as well as chemical property of the PAH being degraded. A wide variety of bacterial, fungal and algal species have the potential to degrade/transform PAHs, among which bacteria and fungi mediated degradation has been studied most extensively. In last few decades microbial community analysis, biochemical pathway for PAHs degradation, gene organization, enzyme system, genetic regulation for PAH degradation have been explored in great detail. Although, xenobiotic-degrading microorganisms have incredible potential to restore contaminated environments inexpensively yet effectively, but new advancements are required to make such microbes effective and more powerful in removing those compounds, which were once thought to be recalcitrant. Recent analytical chemistry and genetic engineering tools might help to improve the efficiency of degradation of PAHs by microorganisms, and minimize uncertainties of successful bioremediation. However, appropriate implementation of the potential of naturally occurring microorganisms for field bioremediation could be considerably enhanced by optimizing certain factors such as bioavailability, adsorption and mass transfer of PAHs. The main

  17. Current State of Knowledge in Microbial Degradation of Polycyclic Aromatic Hydrocarbons (PAHs): A Review

    Science.gov (United States)

    Ghosal, Debajyoti; Ghosh, Shreya; Dutta, Tapan K.; Ahn, Youngho

    2016-01-01

    Polycyclic aromatic hydrocarbons (PAHs) include a group of organic priority pollutants of critical environmental and public health concern due to their toxic, genotoxic, mutagenic and/or carcinogenic properties and their ubiquitous occurrence as well as recalcitrance. The increased awareness of their various adverse effects on ecosystem and human health has led to a dramatic increase in research aimed toward removing PAHs from the environment. PAHs may undergo adsorption, volatilization, photolysis, and chemical oxidation, although transformation by microorganisms is the major neutralization process of PAH-contaminated sites in an ecologically accepted manner. Microbial degradation of PAHs depends on various environmental conditions, such as nutrients, number and kind of the microorganisms, nature as well as chemical property of the PAH being degraded. A wide variety of bacterial, fungal and algal species have the potential to degrade/transform PAHs, among which bacteria and fungi mediated degradation has been studied most extensively. In last few decades microbial community analysis, biochemical pathway for PAHs degradation, gene organization, enzyme system, genetic regulation for PAH degradation have been explored in great detail. Although, xenobiotic-degrading microorganisms have incredible potential to restore contaminated environments inexpensively yet effectively, but new advancements are required to make such microbes effective and more powerful in removing those compounds, which were once thought to be recalcitrant. Recent analytical chemistry and genetic engineering tools might help to improve the efficiency of degradation of PAHs by microorganisms, and minimize uncertainties of successful bioremediation. However, appropriate implementation of the potential of naturally occurring microorganisms for field bioremediation could be considerably enhanced by optimizing certain factors such as bioavailability, adsorption and mass transfer of PAHs. The main

  18. Current state of knowledge in microbial degradation of polycyclic aromatic hydrocarbons (PAHs: a review

    Directory of Open Access Journals (Sweden)

    Debajyoti Ghosal

    2016-08-01

    Full Text Available Polycyclic aromatic hydrocarbons (PAHs include a group of organic priority pollutants of critical environmental and public health concern due to their toxic, genotoxic, mutagenic and/or carcinogenic properties and their ubiquitous occurrence as well as recalcitrance. The increased awareness of their various adverse effects on ecosystem and human health has led to a dramatic increase in research aimed towards removing PAHs from the environment. PAHs may undergo adsorption, volatilization, photolysis, and chemical oxidation, although transformation by microorganisms is the major neutralization process of PAH-contaminated sites in an ecologically accepted manner. Microbial degradation of PAHs depends on various environmental conditions, such as nutrients, number and kind of the microorganisms, nature as well as chemical property of the PAH being degraded. A wide variety of bacterial, fungal and algal species have the potential to degrade/transform PAHs, among which bacteria and fungi mediated degradation has been studied most extensively. In last few decades microbial community analysis, biochemical pathway for PAHs degradation, gene organization, enzyme system, genetic regulation for PAH degradation have been explored in great detail. Although, xenobiotic-degrading microorganisms have incredible potential to restore contaminated environments inexpensively yet effectively, but new advancements are required to make such microbes effective and more powerful in removing those compounds, which were once thought to be recalcitrant. Recent analytical chemistry and genetic engineering tools might help to improve the efficiency of degradation of PAHs by microorganisms, and minimize uncertainties of successful bioremediation. However, appropriate implementation of the potential of naturally occurring microorganisms for field bioremediation could be considerably enhanced by optimizing certain factors such as bioavailability, adsorption and mass transfer of

  19. Current State of Knowledge in Microbial Degradation of Polycyclic Aromatic Hydrocarbons (PAHs): A Review.

    Science.gov (United States)

    Ghosal, Debajyoti; Ghosh, Shreya; Dutta, Tapan K; Ahn, Youngho

    2016-01-01

    Polycyclic aromatic hydrocarbons (PAHs) include a group of organic priority pollutants of critical environmental and public health concern due to their toxic, genotoxic, mutagenic and/or carcinogenic properties and their ubiquitous occurrence as well as recalcitrance. The increased awareness of their various adverse effects on ecosystem and human health has led to a dramatic increase in research aimed toward removing PAHs from the environment. PAHs may undergo adsorption, volatilization, photolysis, and chemical oxidation, although transformation by microorganisms is the major neutralization process of PAH-contaminated sites in an ecologically accepted manner. Microbial degradation of PAHs depends on various environmental conditions, such as nutrients, number and kind of the microorganisms, nature as well as chemical property of the PAH being degraded. A wide variety of bacterial, fungal and algal species have the potential to degrade/transform PAHs, among which bacteria and fungi mediated degradation has been studied most extensively. In last few decades microbial community analysis, biochemical pathway for PAHs degradation, gene organization, enzyme system, genetic regulation for PAH degradation have been explored in great detail. Although, xenobiotic-degrading microorganisms have incredible potential to restore contaminated environments inexpensively yet effectively, but new advancements are required to make such microbes effective and more powerful in removing those compounds, which were once thought to be recalcitrant. Recent analytical chemistry and genetic engineering tools might help to improve the efficiency of degradation of PAHs by microorganisms, and minimize uncertainties of successful bioremediation. However, appropriate implementation of the potential of naturally occurring microorganisms for field bioremediation could be considerably enhanced by optimizing certain factors such as bioavailability, adsorption and mass transfer of PAHs. The main

  20. Degradation of phenolics, nitrogen-heterocyclics and polynuclear aromatic hydrocarbons in a rotating biological contactor.

    Science.gov (United States)

    Jeswani, Hansa; Mukherji, Suparna

    2012-05-01

    The degradation of phenolics, heterocyclics and polynuclear aromatic hydrocarbons (PAHs) in a synthetic biomass gasifier wastewater with average COD of 1388 mg/L was studied in a three stage rotating biological contactor (RBC) using the pyrene degrader, Exiguobacterium aurantiacum and activated sludge consortia (1:3 v/v). As the organic loading rate (OLR) was varied from 3.3 to 14 g/m(2)/d, the COD removal ranged from 63.3% to 92.6%. Complete removal of all the constituents was observed at the lowest OLR of 3.3g/m(2)/d. At 24h hydraulic retention time (HRT) and OLR of 6.6g/m(2)/d complete removal of pyridine, quinoline and benzene and 85-96% removal of phenol, naphthalene, phenanthrene, fluoranthene and pyrene was observed. E. aurantiacum was found to be the dominant bacteria in the biofilm. Clark's model provided good fits to data for all the three stages of the RBC.

  1. Potential of Polycyclic Aromatic Hydrocarbon-Degrading Bacterial Isolates to Contribute to Soil Fertility

    Directory of Open Access Journals (Sweden)

    Maryam Bello-Akinosho

    2016-01-01

    Full Text Available Restoration of polycyclic aromatic hydrocarbon- (PAH- polluted sites is presently a major challenge in agroforestry. Consequently, microorganisms with PAH-degradation ability and soil fertility improvement attributes are sought after in order to achieve sustainable remediation of polluted sites. This study isolated PAH-degrading bacteria from enriched cultures of spent automobile engine-oil polluted soil. Isolates’ partial 16S rRNA genes were sequenced and taxonomically classified. Isolates were further screened for their soil fertility attributes such as phosphate solubilization, atmospheric nitrogen fixation, and indoleacetic acid (IAA production. A total of 44 isolates were obtained and belong to the genera Acinetobacter, Arthrobacter, Bacillus, Flavobacterium, Microbacterium, Ochrobactrum, Pseudomonas, Pseudoxanthomonas, Rhodococcus, and Stenotrophomonas. Data analysed by principal component analysis showed the Bacillus and Ochrobactrum isolates displayed outstanding IAA production. Generalized linear modelling statistical approaches were applied to evaluate the contribution of the four most represented genera (Pseudomonas, Acinetobacter, Arthrobacter, and Rhodococcus to soil fertility. The Pseudomonas isolates were the most promising in all three soil fertility enhancement traits evaluated and all isolates showed potential for one or more of the attributes evaluated. These findings demonstrate a clear potential of the isolates to participate in restorative bioremediation of polluted soil, which will enhance sustainable agricultural production and environmental protection.

  2. Potential of Polycyclic Aromatic Hydrocarbon-Degrading Bacterial Isolates to Contribute to Soil Fertility

    Science.gov (United States)

    Chirima, George Johannes

    2016-01-01

    Restoration of polycyclic aromatic hydrocarbon- (PAH-) polluted sites is presently a major challenge in agroforestry. Consequently, microorganisms with PAH-degradation ability and soil fertility improvement attributes are sought after in order to achieve sustainable remediation of polluted sites. This study isolated PAH-degrading bacteria from enriched cultures of spent automobile engine-oil polluted soil. Isolates' partial 16S rRNA genes were sequenced and taxonomically classified. Isolates were further screened for their soil fertility attributes such as phosphate solubilization, atmospheric nitrogen fixation, and indoleacetic acid (IAA) production. A total of 44 isolates were obtained and belong to the genera Acinetobacter, Arthrobacter, Bacillus, Flavobacterium, Microbacterium, Ochrobactrum, Pseudomonas, Pseudoxanthomonas, Rhodococcus, and Stenotrophomonas. Data analysed by principal component analysis showed the Bacillus and Ochrobactrum isolates displayed outstanding IAA production. Generalized linear modelling statistical approaches were applied to evaluate the contribution of the four most represented genera (Pseudomonas, Acinetobacter, Arthrobacter, and Rhodococcus) to soil fertility. The Pseudomonas isolates were the most promising in all three soil fertility enhancement traits evaluated and all isolates showed potential for one or more of the attributes evaluated. These findings demonstrate a clear potential of the isolates to participate in restorative bioremediation of polluted soil, which will enhance sustainable agricultural production and environmental protection. PMID:27774456

  3. Impact of Inoculation Protocols, Salinity, and pH on the Degradation of Polycyclic Aromatic Hydrocarbons (PAHs) and Survival of PAH-Degrading Bacteria Introduced into Soil

    OpenAIRE

    Kästner, Matthias; Breuer-Jammali, Maren; Mahro, Bernd

    1998-01-01

    Degradation of polycyclic aromatic hydrocarbons (PAHs) and survival of bacteria in soil was investigated by applying different inoculation protocols. The soil was inoculated with Sphingomonas paucimobilis BA 2 and strain BP 9, which are able to degrade anthracene and pyrene, respectively. CFU of soil bacteria and of the introduced bacteria were monitored in native and sterilized soil at different pHs. Introduction with mineral medium inhibited PAH degradation by the autochthonous microflora a...

  4. Degradation of polycyclic aromatic hydrocarbons by free and nanoclay-immobilized manganese peroxidase from Anthracophyllum discolor.

    Science.gov (United States)

    Acevedo, F; Pizzul, L; Castillo, M Dp; González, M E; Cea, M; Gianfreda, L; Diez, M C

    2010-06-01

    Manganese peroxidase (MnP) produced by Anthracophyllum discolor, a Chilean white rot fungus, was immobilized on nanoclay obtained from volcanic soil and its ability to degrade polycyclic aromatic hydrocarbons (PAHs) compared with the free enzyme was evaluated. At the same time, nanoclay characterization was performed. Nanoclay characterization by transmission electronic microscopy showed a particle average size smaller than 100 nm. The isoelectric points (IEP) of nanoclay and MnP from A. discolor were 7.0 and 3.7, respectively, as determined by micro electrophoresis migration and preparative isoelectric focusing. Results indicated that 75% of the enzyme was immobilized on the nanoclay through physical adsorption. As compared to the free enzyme, immobilized MnP from A. discolor achieved an improved stability to temperature and pH. The activation energy (Ea) value for immobilized MnP (51.9 kJ mol(-1)) was higher than that of the free MnP (34.4 kJ mol(-1)). The immobilized enzyme was able to degrade pyrene (>86%), anthracene (>65%), alone or in mixture, and to a less extent fluoranthene (soil. Overall results indicate that nanoclay, a carrier of natural origin, is a suitable support material for MnP immobilization. In addition, immobilized MnP shows an increased stability to high temperature, pH and time storage, as well as an enhanced PAHs degradation efficiency in soil. All these characteristics may suggest the possible use of nanoclay-immobilized MnP from A. discolor as a valuable option for in situ bioremediation purposes. PMID:20435332

  5. Prediction of mono- and polycyclic aromatic hydrocarbon degradation in spiked soils using cyclodextrin extraction

    International Nuclear Information System (INIS)

    In this study, an aqueous-based hydroxypropyl-β-cyclodextrin (HPCD) extraction technique was assessed for its capacity to determine the microbially degradable fraction of mono- and polycyclic aromatic hydrocarbons in four dissimilar soils. A linear relationship (slope = 0.90; R 2 = 0.89), approaching 1:1 between predicted and observed phenanthrene mineralization, was demonstrated for the cyclodextrin extraction; however, the water only extraction underestimated the microbially available fraction by a factor of three (slope = 3.35; R 2 = 0.64). With respect to determining the mineralizable fraction of p-cresol in soils, the cyclodextrin extraction (slope = 0.94; R 2 = 0.84) was more appropriate than the water extraction (slope = 1.50; R 2 = 0.36). Collectively, these results suggested that the cyclodextrin extraction technique was suitable for the prediction of the mineralizable fraction of representative PAHs and phenols present in dissimilar soils following increasing soil-contaminant contact times. The assessment of the microbial availability of contaminants in soils is important for a more representative evaluation of soil contamination. - An aqueous-based HPCD extraction technique was more appropriate than the water extraction in prediction of the mineralizable fraction of phenanthrene and p-cresol present in a range of dissimilar soils

  6. Polynuclear aromatic hydrocarbon degradation by heterogeneous reactions with N 2O 5 on atmospheric particles

    Science.gov (United States)

    Kamens, Richard M.; Guo, Jiazhen; Guo, Zhishi; McDow, Stephen R.

    The degradation of particulate polynuclear aromatic hydrocarbons (PAH) on atmospheric soot particles in the presence of gas phase dinitrogen pentoxide (N 2O 5) was explored. Dilute diesel and wood soot particles containing PAH were reacted with˜10ppm of N 2O 5 in a 200 ℓ continuous stirred tank reactor (CSTR). To provide a stable source of particles for reaction in the CSTR, diesel or wood soot particles were injected at night into a 25 m 3 Teflon outdoor chamber. The large chamber served as a reservoir for the feed aerosol, and the aerosol could then be introduced at a constant flow rate into the CSTR. PAH-N 2O 5 heterogeneous rate constants for wood soot at 15°C ranged from2 × 10 -18to5 × 10 -18 cm 3 molecules -1 s -1. For diesel soot the rate constants at 16°C were higher and ranged from5 × 10 -18to30 × 10 -18 cm 3 molecules -1 s -1. Comparisons with other studies suggest that sunlight is the most important factor which influences PAH decay. This is followed by ozone, NO 2, N 2O 5 and nitric acid. The rate constants of nitro-PAH formation from a parent PAH and N 2O 5 were of the order of1 × 10 -19-1 × 10 -18 molecules -1s -1. The uncertainty associated with all of these rate constants is± a factor of 3. Given, however, the small magnitude of the rate constants and the low levels of N 2O 5 present in the atmosphere, we concluded that PAH heterogeneous reactions with gas phase N 2O 5 degrade particle-bound PAH or to form nitro-PAH from PAH are not very important. (Direct application of the specific rate constants derived in this study to ambient atmospheres should not be undertaken unless the ambient particle size distributions and chemical composition of the particles are similar to the ones reported in this study.)

  7. A quantitative PCR approach for quantification of functional genes involved in the degradation of polycyclic aromatic hydrocarbons in contaminated soils

    Science.gov (United States)

    Shahsavari, Esmaeil; Aburto-Medina, Arturo; Taha, Mohamed; Ball, Andrew S.

    2016-01-01

    Polycyclic aromatic hydrocarbons (PAHs) are major pollutants globally and due to their carcinogenic and mutagenic properties their clean-up is paramount. Bioremediation or using PAH degrading microorganisms (mainly bacteria) to degrade the pollutants represents cheap, effective methods. These PAH degraders harbor functional genes which help microorganisms use PAHs as source of food and energy. Most probable number (MPN) and plate counting methods are widely used for counting PAHs degraders; however, as culture based methods only count a small fraction (soil samples.•This protocol enables us to screen a vast number of PAH contaminated soil samples in few hours.•This protocol provides valuable information about the natural attenuation potential of contaminated soil and can be used to monitor the bioremediation process. PMID:27054096

  8. Superconductivity in aromatic hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Kubozono, Yoshihiro, E-mail: kubozono@cc.okayama-u.ac.jp [Research Laboratory for Surface Science, Okayama University, Okayama 700-8530 (Japan); Research Center of New Functional Materials for Energy Production, Storage and Transport, Okayama University, Okayama 700-8530 (Japan); Japan Science and Technology Agency, ACT-C, Kawaguchi 332-0012 (Japan); Goto, Hidenori; Jabuchi, Taihei [Research Laboratory for Surface Science, Okayama University, Okayama 700-8530 (Japan); Yokoya, Takayoshi [Research Laboratory for Surface Science, Okayama University, Okayama 700-8530 (Japan); Research Center of New Functional Materials for Energy Production, Storage and Transport, Okayama University, Okayama 700-8530 (Japan); Kambe, Takashi [Department of Physics, Okayama University, Okayama 700-8530 (Japan); Sakai, Yusuke; Izumi, Masanari; Zheng, Lu; Hamao, Shino; Nguyen, Huyen L.T. [Research Laboratory for Surface Science, Okayama University, Okayama 700-8530 (Japan); Sakata, Masafumi; Kagayama, Tomoko; Shimizu, Katsuya [Center of Science and Technology under Extreme Conditions, Osaka University, Osaka 560-8531 (Japan)

    2015-07-15

    Highlights: • Aromatic superconductor is one of core research subjects in superconductivity. Superconductivity is observed in certain metal-doped aromatic hydrocarbons. Some serious problems to be solved exist for future advancement of the research. This article shows the present status of aromatic superconductors. - Abstract: ‘Aromatic hydrocarbon’ implies an organic molecule that satisfies the (4n + 2) π-electron rule and consists of benzene rings. Doping solid aromatic hydrocarbons with metals provides the superconductivity. The first discovery of such superconductivity was made for K-doped picene (K{sub x}picene, five benzene rings). Its superconducting transition temperatures (T{sub c}’s) were 7 and 18 K. Recently, we found a new superconducting K{sub x}picene phase with a T{sub c} as high as 14 K, so we now know that K{sub x}picene possesses multiple superconducting phases. Besides K{sub x}picene, we discovered new superconductors such as Rb{sub x}picene and Ca{sub x}picene. A most serious problem is that the shielding fraction is ⩽15% for K{sub x}picene and Rb{sub x}picene, and it is often ∼1% for other superconductors. Such low shielding fractions have made it difficult to determine the crystal structures of superconducting phases. Nevertheless, many research groups have expended a great deal of effort to make high quality hydrocarbon superconductors in the five years since the discovery of hydrocarbon superconductivity. At the present stage, superconductivity is observed in certain metal-doped aromatic hydrocarbons (picene, phenanthrene and dibenzopentacene), but the shielding fraction remains stubbornly low. The highest priority research area is to prepare aromatic superconductors with a high superconducting volume-fraction. Despite these difficulties, aromatic superconductivity is still a core research target and presents interesting and potentially breakthrough challenges, such as the positive pressure dependence of T{sub c} that is clearly

  9. The polycyclic aromatic hydrocarbon degradation potential of Gulf of Mexico coastal microbial communities after the Deepwater Horizon oil spill

    Directory of Open Access Journals (Sweden)

    Anthony D. Kappell

    2014-05-01

    Full Text Available The Deepwater Horizon (DWH blowout resulted in oil transport, including polycyclic aromatic hydrocarbons (PAHs to the Gulf of Mexico shoreline. The microbial communities of these shorelines are thought to be responsible for the intrinsic degradation of PAHs. To investigate the Gulf Coast beach microbial community response to hydrocarbon exposure, we examined the functional gene diversity, bacterial community composition, and PAH degradation capacity of a heavily oiled and non-oiled beach following the oil exposure. With a non-expression functional gene microarray targeting 539 gene families, we detected 28,748 coding sequences. Of these sequences, 10% were uniquely associated with the severely oil-contaminated beach and 6.0% with the non-oiled beach. There was little variation in the functional genes detected between the two beaches; however the relative abundance of functional genes involved in oil degradation pathways, including PAHs, were greater in the oiled beach. The microbial PAH degradation potentials of both beaches, were tested in mesocosms. Mesocosms were constructed in glass columns using sands with native microbial communities, circulated with artificial sea water and challenged with a mixture of PAHs. The low-molecular weight PAHs, fluorene and naphthalene, showed rapid depletion in all mesocosms while the high-molecular weight benzo[α]pyrene was not degraded by either microbial community. Both the heavily oiled and the non-impacted coastal communities showed little variation in their biodegradation ability for low molecular weight PAHs. Massively-parallel sequencing of 16S rRNA genes from mesocosm DNA showed that known PAH degraders and genera frequently associated with oil hydrocarbon degradation represented a major portion of the bacterial community. The observed similar response by microbial communities from beaches with a different recent history of oil exposure suggests that Gulf Coast beach communities are primed for PAH

  10. Genomic insights into the metabolic potential of the polycyclic aromatic hydrocarbon degrading sulfate-reducing Deltaproteobacterium N47.

    Science.gov (United States)

    Bergmann, Franz; Selesi, Draženka; Weinmaier, Thomas; Tischler, Patrick; Rattei, Thomas; Meckenstock, Rainer U

    2011-05-01

    Anaerobic degradation of polycyclic aromatic hydrocarbons (PAHs) is an important process during natural attenuation of aromatic hydrocarbon spills. However, knowledge about metabolic potential and physiology of organisms involved in anaerobic degradation of PAHs is scarce. Therefore, we introduce the first genome of the sulfate-reducing Deltaproteobacterium N47 able to catabolize naphthalene, 2-methylnaphthalene, or 2-naphthoic acid as sole carbon source. Based on proteomics, we analysed metabolic pathways during growth on PAHs to gain physiological insights on anaerobic PAH degradation. The genomic assembly and taxonomic binning resulted in 17 contigs covering most of the sulfate reducer N47 genome according to general cluster of orthologous groups (COGs) analyses. According to the genes present, the Deltaproteobacterium N47 can potentially grow with the following sugars including d-mannose, d-fructose, d-galactose, α-d-glucose-1P, starch, glycogen, peptidoglycan and possesses the prerequisites for butanoic acid fermentation. Despite the inability for culture N47 to utilize NO(3) (-) as terminal electron acceptor, genes for nitrate ammonification are present. Furthermore, it is the first sequenced genome containing a complete TCA cycle along with the carbon monoxide dehydrogenase pathway. The genome contained a significant percentage of repetitive sequences and transposase-related protein domains enhancing the ability of genome evolution. Likewise, the sulfate reducer N47 genome contained many unique putative genes with unknown function, which are candidates for yet-unknown metabolic pathways.

  11. Effects of soil organic matter on the development of the microbial polycyclic aromatic hydrocarbons (PAHs) degradation potentials

    International Nuclear Information System (INIS)

    The microbial activity in soils was a critical factor governing the degradation of organic micro-pollutants. The present study was conducted to analyze the effects of soil organic matter on the development of degradation potentials for polycyclic aromatic hydrocarbons (PAHs). Most of the degradation kinetics for PAHs by the indigenous microorganisms developed in soils can be fitted with the Logistic growth models. The microbial activities were relatively lower in the soils with the lowest and highest organic matter content, which were likely due to the nutrition limit and PAH sequestration. The microbial activities developed in humic acid (HA) were much higher than those developed in humin, which was demonstrated to be able to sequester organic pollutants stronger. The results suggested that the nutrition support and sequestration were the two major mechanisms, that soil organic matter influenced the development of microbial PAHs degradation potentials. - Research highlights: → PAH degradation kinetics obey Logistic model. → Degradation potentials depend on soil organic carbon content. → Humin inhibits the development of PAH degradation activity. → Nutrition support and sequestration regulate microbial degradation capacity. - Soil organic matter regulated PAH degradation potentials through nutrition support and sequestration.

  12. Photocatalytic degradation of polycyclic aromatic hydrocarbons on soil surfaces using TiO2 under UV light

    International Nuclear Information System (INIS)

    The photocatalytic degradation of phenanthrene (PHE), pyrene (PYRE) and benzo[a]pyrene (BaP) on soil surfaces in the presence of TiO2 using ultraviolet (UV) light source was investigated in a photo chamber, in which the temperature was maintained 30 deg. C. The effects of various factors, namely TiO2, soil pH, humic acid, and UV wavelength, on the degradation performance of polycyclic aromatic hydrocarbons (PAHs) were studied. The results show that photocatalytic degradation of PAHs follows the pseudo-first-order kinetics. Catalyst TiO2 accelerated the photodegradation of PHE, PYRE and BaP significantly, with their half-lives being reduced from 533.15 to 130.77 h, 630.09 to 192.53 h and 363.22 to 103.26 h, respectively, when the TiO2 content was 0.5%. In acidic or alkaline conditions, the photocatalytic degradation rates of the PAHs were greater than those in neutral conditions. Humic acid significantly enhanced the PAH photocatalytic degradation by sensitizing radicals capable of oxidizing PAHs. Photocatalytic degradation rates of PYRE and BaP on soil surfaces with 2% TiO2 were different at UV irradiation wavelengths of 254, 310 and 365 nm, respectively. The synergistic effect of UV irradiation and TiO2 catalysis was efficient for degradation of PAHs in contaminated soil

  13. Degradation of polycyclic aromatic hydrocarbons in crumb tyre rubber catalysed by rutile TiO2 under UV irradiation.

    Science.gov (United States)

    Yu, Kai; Huang, Linyue; Lou, Lan-Lan; Chang, Yue; Dong, Yanling; Wang, Huan; Liu, Shuangxi

    2015-01-01

    The polycyclic aromatic hydrocarbons (PAHs) in crumb tyre rubber were firstly degraded under UV irradiation in the presence of rutile TiO2 and hydrogen peroxide. The effects of light intensity, catalyst amount, oxidant amount, initial pH value, co-solvent content, and reaction time on degradation efficiency of typical PAHs in crumb tyre rubber were studied. The results indicated that UV irradiation, rutile TiO2, and hydrogen peroxide were beneficial to the degradation of PAHs and co-solvent could accelerate the desorption of PAHs from crumb tyre rubber. Up to 90% degradation efficiency of total 16 PAHs could be obtained in the presence of rutile TiO2 (1 wt%) and hydrogen peroxide (1.0 mL) under 1800 µW cm(-2) UV irradiation for 48 h. The high molecular weight PAHs (such as benz(a)pyrene) were more difficult to be degraded than low molecular weight PAHs (such as phenanthrene, chrysene). Moreover, through the characterization of reaction solution and degradation products via GC-MS, it was proved that the PAHs in crumb tyre rubber were successfully degraded. PMID:25323028

  14. Microbial Degradation of Phenols and Aromatic Hydrocarbons in Creosote-contaminated Groundwater Under Nitrate-reducing Conditions

    DEFF Research Database (Denmark)

    Flyvbjerg, John; Arvin, Erik; Jensen, Bjørn K.;

    1993-01-01

    Batch experiments were carried out to investigate the biodegradation of phenols and aromatic hydrocarbons under anaerobic, nitrate-reducing conditions in groundwater from a creosote-contaminated site at Fredensborg, Denmark. The bacteria in the creosote-contaminated groundwater degraded a mixture...... of toluene, phenol, the cresols (o-, m- and p-cresol) and the dimethylphenols 2,4-DMP and 3,4-DMP at both 10° and 20°C. Benzene, the xylenes, napthalene, 2,3-DMP, 2,5-DMP, 2,6-DMP and 3,5-DMP were resistant to biodegradation during 7–12 months of incubation. It was demonstrated that the degradation...... of toluene, 2,4-DMP, 3,4-DMP and p-cresol depended on nitrate or nitrite as electron acceptors. 40–80% of the nitrate consumed during degradation of the aromatic compounds was recovered as nitrite, and the consumption of nitrate was accompanied by a production of ATP. Stoichiometric calculations indicated...

  15. Draft Genome Sequence of Pseudomonas sp. Strain 10-1B, a Polycyclic Aromatic Hydrocarbon Degrader in Contaminated Soil

    OpenAIRE

    Bello-Akinosho, Maryam; Adeleke, Rasheed; Swanevelder, Dirk; Thantsha, Mapitsi

    2015-01-01

    Pseudomonas sp. strain 10-1B was isolated from artificially polluted soil after selective enrichment. Its draft genome consists of several predicted genes that are involved in the hydroxylation of the aromatic ring, which is the rate-limiting step in the biodegradation of polycyclic aromatic hydrocarbons.

  16. Complete Genome Sequence of a Bacterium Representing a Deep Uncultivated Lineage within the Gammaproteobacteria Associated with the Degradation of Polycyclic Aromatic Hydrocarbons

    Science.gov (United States)

    Dickey, Allison N.; Scholl, Elizabeth H.; Wright, Fred A.; Aitken, Michael D.

    2016-01-01

    The bacterial strain TR3.2, representing a novel deeply branching lineage within the Gammaproteobacteria, was isolated and its genome sequenced. This isolate is the first cultivated representative of the previously described “Pyrene Group 2” (PG2) and represents a variety of environmental sequences primarily associated with petrochemical contamination and aromatic hydrocarbon degradation.

  17. Bacterial Degradation of Aromatic Compounds

    Directory of Open Access Journals (Sweden)

    Qing X. Li

    2009-01-01

    Full Text Available Aromatic compounds are among the most prevalent and persistent pollutants in the environment. Petroleum-contaminated soil and sediment commonly contain a mixture of polycyclic aromatic hydrocarbons (PAHs and heterocyclic aromatics. Aromatics derived from industrial activities often have functional groups such as alkyls, halogens and nitro groups. Biodegradation is a major mechanism of removal of organic pollutants from a contaminated site. This review focuses on bacterial degradation pathways of selected aromatic compounds. Catabolic pathways of naphthalene, fluorene, phenanthrene, fluoranthene, pyrene, and benzo[a]pyrene are described in detail. Bacterial catabolism of the heterocycles dibenzofuran, carbazole, dibenzothiophene, and dibenzodioxin is discussed. Bacterial catabolism of alkylated PAHs is summarized, followed by a brief discussion of proteomics and metabolomics as powerful tools for elucidation of biodegradation mechanisms.

  18. The Effect of Interaction Between White-rot Fungi and Indigenous Microorganisms on Degradation of Polycyclic Aromatic Hydrocarbons in Soil

    Energy Technology Data Exchange (ETDEWEB)

    Wiesche, C. in der [Institute of Plant Nutrition and Soil Science, Federal Agricultural Research Centre (Germany)], E-mail: carsten.wiesche@fal.de; Martens, R. [Institute of Agroecology, Federal Agricultural Research Centre (Germany); Zadrazil, F. [Institute of Plant Nutrition and Soil Science, Federal Agricultural Research Centre (Germany)

    2003-05-15

    White-rot fungi applied for soil bioremediation have to compete with indigenous soil microorganisms. The effect of competition on both indigenous soil microflora and white-rot fungi was evaluated with regard to degradation of polycyclic aromatic hydrocarbons (PAH) with different persistence in soil. Sterile and non-sterile soil was artificially contaminated with {sup 14}C-labeled PAH consisting of three (anthracene), four (pyrene, benz[a]anthracene) and five fused aromatic rings (benzo[a]pyrene, dibenz[a,h]anthracene). The two fungi tested,Dichomitus squalens and Pleurotus ostreatus, produced similar amounts of ligninolytic enzymes in soil, but PAH mineralization by P. ostreatus was significantly higher. Compared to the indigenous soil microflora, P.ostreatus mineralized 5-ring PAH to a larger extent, while the indigenous microflora was superior in mineralizing 3-ring and 4-ring PAH. In coculture the special capabilities of both soil microflora and P. ostreatus were partly restricted due to antagonistic interactions, but essentially preserved. Thus, soil inoculation with P. ostreatus significantly increased the mineralization of high-molecular-weight PAH, and at the same time reduced the mineralization of anthracene and pyrene. Regarding the mineralization of low-molecular-weight PAH, the stimulation of indigenous soil microorganisms by straw amendment was more efficient than application of white-rot fungi.

  19. Interaction between Carbon Nanotubes and Aromatic Hydrocarbon-degrading Microbes and its Effect on Carbon Nanotubes Transformation

    Science.gov (United States)

    You, Y.; Wang, L.; Poulson, S.; Wang, X.; Xing, B.; Yang, Y.

    2015-12-01

    Due to their unique electrical, optical and mechanical properties, carbon nanotubes (CNTs) have been substantially produced and widely applied during the past decades, leading to their increased probability of entering the environment. Some estimation suggests that CNTs are accumulated in agricultural systems with their soil concentration increasing by 0.4-157 ng/kg/year. This has raised concerns about environmental impacts of these emerging contaminants including their ecotoxicity. Meanwhile, transformation of CNTs in the environment can significantly affect their transport, bioavailability and thereby ecotoxicity. So far, environmental biodegradation of CNTs remains obscure. Given the high diversity of soil microorganisms and their metabolic potentials, it is important to investigate microbial biodegradation of CNTs under various environmental conditions. This study focuses on an aromatic hydrocarbon-degrading bacterium, Mycobacterium vanbaalenii PYR-1, as a model microorganism capable of ring cleavage. We hypothesize that bacterial activities could transform CNTs to more hydrophilic forms, increasing their aqueous stability and environmental reactivity. We incubated M. vanbaalenii PYR-1 with 13C-labeded multiwall carbon nanotubes (MWCNTs) for 30 days, monitored δ13C in the system, characterized MWCNTs before and after the reaction, and compared the results with culture-negative controls. To investigate effects of various environmental conditions, including the presence of extracellular oxidative enzymes from white-rot fungi, additional experiments will be conducted and results compared will be compared among different setups. Moreover, we will measure adverse impacts of CNTs on the metabolic activities of M. vanbaalenii PYR-1, particularly its biodegradation of polycyclic aromatic hydrocarbons.

  20. Degradation of polycyclic aromatic hydrocarbons by Pseudomonas sp.JM2 isolated from active sewage sludge of chemical plant

    Institute of Scientific and Technical Information of China (English)

    Jing Ma; Li Xu; Lingyun Jia

    2012-01-01

    It is important to screen strains that can decompose polycyclic aromatic hydrocarbons (PAHs) completely and rapidly with good adaptability for bioremediation in a local area.A bacterial strain JM2,which uses phenanthrene as its sole carbon source,was isolated from the active sewage sludge from a chemical plant in Jilin,China and identified as Pseudomonas based on 16S rDNA gene sequence analysis.Although the optimal growth conditions were determined to be pH 6.0 and 37℃,JM2 showed a broad pH and temperature profile.At pH 4.5 and 9.3,JM2 could degrade more than 40% of fluorene and phenanthrene (50 mg/L each) within 4 days.In addition,when the temperature was as low as 4℃,JM2 could degrade up to 24% fluorene and 12% phenanthrene.This showed the potential for JM2 to be applied in bioremediation over winter or in cold regions.Moreover,a nutrient augmentation study showed that adding formate into media could promote PAH degradation,while the supplement of salicylate had an inhibitive effect.Furthermore,in a metabolic pathway study,salicylate,phthaiic acid,and 9-fluorenone were detected during the degradation of fluorene or phenanthrene.In conclusion,Pseudomonas sp.JM2 is a high performance strain in the degradation of fluorene and phenanthrene under extreme pH and temperature conditions.It might be useful in the bioremediation of PAHs.

  1. [Study on degradation of polycyclic aromatic hydrocarbons (PAHs) with different additional carbon sources in aged contaminated soil].

    Science.gov (United States)

    Yin, Chun-Qin; Jiang, Xin; Wang, Fang; Wang, Cong-Ying

    2012-02-01

    This study was conducted with different additional carbon sources (such as: glucose, DL-malic acid, citrate, urea and ammonium acetate) to elucidate the degradation of polycyclic aromatic hydrocarbons (PAHs) in aged contaminated soil under an indoor simulation experiment. The results showed that the quantity of CO2 emission in different additional carbon sources treatments was obviously much more than that of check treatment in the first week, and the quantity of CO2 emission in DL-malic acid treatment was the largest. The average CO2 production decreased in an order urea > glucose approximately citrate approximately DL-malic acid approximately ammonium acetate > check. Meanwhile, the amount of volatized PAHs in applied carbon sources treatments was significantly less than that in check treatment. The amount of three volatized PAHs decreased in an order phenanthrene > fluoranthene > benzo(b)fluoranthene. Compared with the check treatment, the average degradation rates of the three PAHs were significantly augmented in the supplied carbon sources treatments, in which rates of the three PAHs were much higher in DL-malic acid and urea treatments than those in other treatments. The largest proportion of residual was benzo(b)fluoranthene (from 72% to 81%) among three PAHs compounds, followed by fluoranthene (from 53% to 70% ) and phenanthrene (from 27% to 44%).

  2. Analysis of annatto (Bixa orellana) food coloring formulations. 2. Determination of aromatic hydrocarbon thermal degradation products by gas chromatography.

    Science.gov (United States)

    Scotter, M J; Wilson, L A; Appleton, G P; Castle, L

    2000-02-01

    Twenty samples of commercial annatto formulations have been analyzed for m-xylene and toluene using ambient alkaline hydrolysis, followed by solvent extraction and capillary gas chromatography. Fifteen of the samples contained <5 mg/kg toluene, four samples contained between 5 and 10 mg/kg toluene, and one sample contained 12 mg/kg toluene. The amounts found of m-xylene were 200 mg/kg (one sample), 160 mg/kg (one sample), between 30 and 88 mg/kg (four samples), between 7 and 25 mg/kg (seven samples), and <5 mg/kg (seven samples). Bixin-in-oil formulations contained the highest m-xylene concentrations and also gave the largest increase in headspace m-xylene concentration when heated in closed systems. The results are evidence for the thermal degradation of annatto during source extraction and processing, resulting in contamination by internal generation of both bixin and norbixin types with aromatic hydrocarbons. Two samples of norbixin of known production history (i. e., thermal versus nonthermal processes) were analyzed specifically to identify possible differences in their degradation component profiles. They were found to differ significantly in m-xylene content, which is consistent with their respective production histories. PMID:10691661

  3. Strong Impact on the Polycyclic Aromatic Hydrocarbon (PAH)-Degrading Community of a PAH-Polluted Soil but Marginal Effect on PAH Degradation when Priming with Bioremediated Soil Dominated by Mycobacteria▿

    OpenAIRE

    Johnsen, Anders R.; Schmidt, Stine; Hybholt, Trine K.; Henriksen, Sidsel; Jacobsen, Carsten S.; Andersen, Ole

    2007-01-01

    Bioaugmentation of soil polluted with polycyclic aromatic hydrocarbons (PAHs) is often disappointing because of the low survival rate and low activity of the introduced degrader bacteria. We therefore investigated the possibility of priming PAH degradation in soil by adding 2% of bioremediated soil with a high capacity for PAH degradation. The culturable PAH-degrading community of the bioremediated primer soil was dominated by Mycobacterium spp. A microcosm containing pristine soil artificial...

  4. Production of alkyl aromatic hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Bonacci, J.C.; Billings, R.P.

    1975-01-30

    An improved method is claimed for producing aromatic hydrocarbons from a hydrocarbon charge containing aromatic hydrocarbons including benzene and C/sub 8/ alkyl aromatics and aliphatic hydrocarbons which charge is rich in such aromatic hydrocarbons and lean in aliphatic hydrocarbons boiling above about 220/sup 0/F by reason of conversion under severe conditions which comprises subjecting said charge to distillation conditions of temperature and pressure such that at least a portion of the benzene content of said fraction is separated as vapor from an alkyl aromatic fraction containing aliphatic hydrocarbons and the major portion of C/sub 8/ aromatics in said charge, reacting said alkyl aromatic fraction in the presence of hydrogen in contact with a catalyst containing type ZSM-5 zeolite, zeolite ZSM-12, zeolite ZSM-21 or zeolite beta in combination with a hydrogenation/dehydrogenation component at conversion conditions to convert aliphatic hydrocarbons to lower boiling material of five carbon atoms and lighter separable from aromatics by distillation including a temperature of about 500/sup 0/ to 1000/sup 0/F, a pressure of about 100 to about 600 pounds, a hydrogen to hydrocarbon mol ratio of 0.2 to 8 and weight hourly space velocity of 0.5 to 15, concurrently contacting a mixture of hydrogen and toluene with a disproportionation catalyst under reaction conditions to disproportionate said toluene, combining the effluents of said contacting steps, separating hydrogen from the combined effluents of said contacting steps, separating hydrogen from the combined effluents, recycling at least a portion of said separated hydrogen to said contacting steps, distilling the hydrocarbon residue from said separation step to recover therefrom at least toluene and mixed xylenes, and recycling at least a portion of said recovered toluene as feed to the disproportionation step aforesaid.

  5. Electrochemical degradation of polycyclic aromatic hydrocarbons in creosote solution using ruthenium oxide on titanium expanded mesh anode.

    Science.gov (United States)

    Tran, Lan-Huong; Drogui, Patrick; Mercier, Guy; Blais, Jean-François

    2009-05-30

    In this study, expanded titanium (Ti) covered with ruthenium oxide (RuO(2)) electrode was used to anodically oxidize polycyclic aromatic hydrocarbons (PAH) in creosote solution. Synthetic creosote-oily solution (COS) was prepared with distilled water and a commercial creosote solution in the presence of an amphoteric surfactant; Cocamidopropylhydroxysultaine (CAS). Electrolysis was carried out using a parallelepipedic electrolytic 1.5-L cell containing five anodes (Ti/RuO(2)) and five cathodes (stainless steel, 316 L) alternated in the electrode pack. The effects of initial pH, temperature, retention time, supporting electrolyte, current density and initial PAH concentration on the process performance were examined. Experimental results revealed that a current density of 9.23 mA cm(-2) was beneficial for PAH oxidation. The sum of PAH concentrations for 16 PAHs could be optimally diminished up to 80-82% while imposing a residence time in the electrolysis cell of 90 min. There was not a significant effect of the electrolyte (Na(2)SO(4)) concentration on oxidation efficiency in the investigated range of 500-4000 mg/L. However, an addition of 500 mg Na(2)SO(4)L(-1) was required to reduce the energy consumption and the treatment cost. Besides, there was no effect of initial PAH concentration on oxidation efficiency in the investigated range of 270-540 mg PAHL(-1). Alkaline media was not favourable for PAH oxidation, whereas high performance of PAH degradation could be recorded without initial pH adjustment (original pH around 6.0). Likewise, under optimal conditions, 84% of petroleum hydrocarbon (C(10)-C(50)) was removed, whereas removal yields of 69% and 62% have been measured for O&G and COD, respectively. Microtox and Daphnia biotests showed that electrochemical oxidation using Ti/RuO(2) could be efficiently used to reduce more than 90% of the COS toxicity. PMID:18926633

  6. Bioassay of polycyclic aromatic hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Van Kirk, E.A.

    1980-08-01

    A positive relationship was found between the photodynamic activity of 24 polycyclic aromatic hydrocarbons versus published results on the mutagenicity, carcinogenicity, and initiation of unscheduled DNA synthesis. Metabolic activation of benzo(a)pyrene resulted in detection of increased mutagenesis in Paramecium tetraurelia as found also in the Ames Salmonella assay. The utility of P. tetraurelia as a biological detector of hazardous polycyclic aromatic hydrocarbons is discussed.

  7. Application of a biofilm formed by a mixture of yeasts isolated in Vietnam to degrade aromatic hydrocarbon polluted wastewater collected from petroleum storage.

    Science.gov (United States)

    Nhi Cong, Le Thi; Ngoc Mai, Cung Thi; Thanh, Vu Thi; Nga, Le Phi; Minh, Nghiem Ngoc

    2014-01-01

    In this study, three good biofilm-forming yeast strains, including Candida viswanathii TH1, Candida tropicalis TH4 and Trichosporon asahii B1, were isolated from oil-contaminated water and sediment samples collected in coastal zones of Vietnam. These strains were registered in the GenBank database with the accession numbers JX129175, JX129176 and KC139404 for strain TH1, TH4 and B1, respectively. The biofilm formed by a mixture of these organisms degraded 90, 85, 82 and 67% of phenol, naphthalene, anthracene and pyrene, respectively, after a 7-day incubation period using an initial concentration of 600 ppm phenol and 200 ppm of each of the other compounds. In addition, this biofilm completely degraded these aromatic compounds, which were from wastewater collected from petroleum tanks in Do Xa, Hanoi after 14 days of incubation based on gas chromatography mass spectrometry analysis. To the best of our knowledge, reports on polycyclic aromatic hydrocarbon and phenol degradation by biofilm-forming yeasts are limited. The results obtained indicate that the biofilm formed by multiple yeast strains may considerably increase the degradation efficiency of aromatic hydrocarbon compounds, and may lead to a new approach for eliminating petroleum oil-contaminated water in Vietnam.

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

    Science.gov (United States)

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

    2014-09-01

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

  9. Screening and degrading characteristics and community structure of a high molecular weight polycyclic aromatic hydrocarbon-degrading bacterial consortium from contaminated soil

    Institute of Scientific and Technical Information of China (English)

    Run Sun; Jinghua Jin; Guangdong Sun; Ying Liu; Zhipei Liu

    2010-01-01

    Inoculation with efficient microbes had been proved to be the most important way for the bioremediation of polluted environments.For the treatment of abandoned site of Beijing Coking Chemical Plant contaminated with high level of high-molecular-weight polycyclic aromatic hydrocarbons (HMW-PAHs),a bacterial consortium capable of degrading HMW-PAHs,designated 1-18-1,was enriched and screened from HMW-PAHs contaminated soil.Its degrading ability was analyzed by high performance liquid chromatography (HPLC),and the community structure was investigated by construction and analyses of the 16S rRNA gene clone libraries (A,B and F) at different transfers.The results indicated that 1-18-1 was able to utilize pyrene,fluoranthene and benzo[a]pyrene as sole carbon and energy source for growth.The degradation rate of pyrene and fluoranthene reached 82.8% and 96.2% after incubation for 8 days at 30℃,respectively;while the degradation rate of benzo[a]pyrene was only 65.1% after incubation for 28 days at 30℃.Totally,108,100 and 100 valid clones were randomly selected and sequenced from the libraries A,B,and E Phylogenetic analyses showed that all the clones could be divided into 5 groups,Bacteroidetes,α-Proteobacteria,Actinobacteria,β-Proteobacteria and γ-Proteobacteria.Sequence similarity analyses showed total 39 operational taxonomic units (OTUs) in the libraries.The predominant bacterial groups were α-Proteobacteria (19 OTUs,48.7%),γ-Proteobacteria (9 OTUs,23.1%) and β-Protcobacteria (8 OTUs,20.5%).During the transfer process,the proportions of α-Proteobacteria and β-Proteobacteria increased greatly (from 47% to 93%),while γ-Proteobacteria decreased from 32% (library A) to 6% (library F);and Bacteroidetes group disappeared in libraries B and F.

  10. Electrochemical degradation of polycyclic aromatic hydrocarbons in creosote solution using ruthenium oxide on titanium expanded mesh anode

    Energy Technology Data Exchange (ETDEWEB)

    Tran, Lan-Huong; Drogui, Patrick; Mercier, Guy [Institut National de la Recherche Scientifique (Centre Eau Terre et Environnement), Universite du Quebec, 490 rue de la Couronne, C.P. 7500, Quebec, Qc G1K 9A9 (Canada); Blais, Jean-Francois, E-mail: blaisjf@ete.inrs.ca [Institut National de la Recherche Scientifique (Centre Eau Terre et Environnement), Universite du Quebec, 490 rue de la Couronne, C.P. 7500, Quebec, Qc G1K 9A9 (Canada)

    2009-05-30

    In this study, expanded titanium (Ti) covered with ruthenium oxide (RuO{sub 2}) electrode was used to anodically oxidize polycyclic aromatic hydrocarbons (PAH) in creosote solution. Synthetic creosote-oily solution (COS) was prepared with distilled water and a commercial creosote solution in the presence of an amphoteric surfactant; Cocamidopropylhydroxysultaine (CAS). Electrolysis was carried out using a parallelepipedic electrolytic 1.5-L cell containing five anodes (Ti/RuO{sub 2}) and five cathodes (stainless steel, 316L) alternated in the electrode pack. The effects of initial pH, temperature, retention time, supporting electrolyte, current density and initial PAH concentration on the process performance were examined. Experimental results revealed that a current density of 9.23 mA cm{sup -2} was beneficial for PAH oxidation. The sum of PAH concentrations for 16 PAHs could be optimally diminished up to 80-82% while imposing a residence time in the electrolysis cell of 90 min. There was not a significant effect of the electrolyte (Na{sub 2}SO{sub 4}) concentration on oxidation efficiency in the investigated range of 500-4000 mg/L. However, an addition of 500 mg Na{sub 2}SO{sub 4} L{sup -1} was required to reduce the energy consumption and the treatment cost. Besides, there was no effect of initial PAH concentration on oxidation efficiency in the investigated range of 270-540 mg PAH L{sup -1}. Alkaline media was not favourable for PAH oxidation, whereas high performance of PAH degradation could be recorded without initial pH adjustment (original pH around 6.0). Likewise, under optimal conditions, 84% of petroleum hydrocarbon (C{sub 10}-C{sub 50}) was removed, whereas removal yields of 69% and 62% have been measured for O and G and COD, respectively. Microtox and Daphnia biotests showed that electrochemical oxidation using Ti/RuO{sub 2} could be efficiently used to reduce more than 90% of the COS toxicity.

  11. Functional genes to assess nitrogen cycling and aromatic hydrocarbon degradation: primers and processing matter

    Directory of Open Access Journals (Sweden)

    Christopher Ryan Penton

    2013-09-01

    Full Text Available Targeting sequencing to genes involved in key environmental processes, i.e. ecofunctional genes, provides an opportunity to sample nature’s gene guilds to greater depth and help link community structure to process-level outcomes. Vastly different approaches have been implemented for sequence processing and, ultimately, for taxonomic placement of these gene reads. The overall quality of next generation sequence analysis of functional genes is dependent on multiple steps and assumptions of unknown diversity. To illustrate current issues surrounding amplicon read processing we provide examples for three ecofunctional gene groups. A combination of in-silico, environmental and cultured strain sequences was used to test new primers targeting the dioxin and dibenzofuran degrading genes dxnA1, dbfA1, and carAa. The majority of obtained environmental sequences were classified into novel sequence clusters, illustrating the discovery value of the approach. For the nitrite reductase step in denitrification, the well-known nirK primers exhibited deficiencies in reference database coverage, illustrating the need to refine primer-binding sites and/or to design multiple primers, while nirS primers exhibited bias against five phyla. Amino acid-based OTU clustering of these two N-cycle genes from soil samples yielded only 114 unique nirK and 45 unique nirS genus-level groupings, likely a reflection of constricted primer coverage. Finally, supervised and non-supervised OTU analysis methods were compared using the nifH gene of nitrogen fixation, with generally similar outcomes, but the clustering (non-supervised method yielded higher diversity estimates and stronger site-based differences. High throughput amplicon sequencing can provide inexpensive and rapid access to nature’s related sequences by circumventing the culturing barrier, but each unique gene requires individual considerations in terms of primer design and sequence processing and classification.

  12. Isolation of Marine Polycyclic Aromatic Hydrocarbon (PAH)-Degrading Cycloclasticus Strains from the Gulf of Mexico and Comparison of Their PAH Degradation Ability with That of Puget Sound Cycloclasticus Strains

    OpenAIRE

    Geiselbrecht, Allison D.; Hedlund, Brian P.; Tichi, Mary A.; Staley, J T

    1998-01-01

    Phenanthrene- and naphthalene-degrading bacteria were isolated from four offshore and nearshore locations in the Gulf of Mexico by using a modified most-probable-number technique. The concentrations of these bacteria ranged from 102 to 106 cells per ml of wet surficial sediment in mildly contaminated and noncontaminated sediments. A total of 23 strains of polycyclic aromatic hydrocarbon (PAH)-degrading bacteria were obtained. Based on partial 16S ribosomal DNA sequences and phenotypic charact...

  13. Degradation of polycyclic aromatic hydrocarbons (PAHs) by a mixed culture and its component pure cultures, obtained from PAH-contaminated soil

    Energy Technology Data Exchange (ETDEWEB)

    Trzesicka-Mlynarz, D.; Ward, O. P.

    1995-06-01

    A mixed culture, isolated from soil contaminated with polycyclic aromatic hydrocarbons (PAHs) grew on and degraded fluoranthene in aqueous media supplemented with glucose, yeast extract and peptone. A pure culture of Pseudomona sp. strain HL7b which was known to degrade fluoranthene was incorporated into initial experiments for comparative purposes. Increased complex nitrogen levels in the aqueous media promoted bacteria growth, and fluoranthene degradation, while high glucose levels diminished fluoranthene degradation. The mixed culture containing 4 Gram-negative rods biodegraded the PAH mixture better than the pure culture. Pure cultures exhibited a good capacity for removal of more water-soluble PAHs, but a lesser capacity for low water-soluble PAHs. 4 tabs., 3 figs., 26 refs.

  14. Degradation of some representative polycyclic aromatic hydrocarbons by the water-soluble protein extracts from Zea mays L. cv PR32-B10.

    Science.gov (United States)

    Barone, Roberto; de Biasi, Margherita-Gabriella; Piccialli, Vincenzo; de Napoli, Lorenzo; Oliviero, Giorgia; Borbone, Nicola; Piccialli, Gennaro

    2016-10-01

    The ability of the water-soluble protein extracts from Zea mais L. cv. PR32-B10 to degrade some representative polycyclic aromatic hydrocarbons (PAHs), has been evaluated. Surface sterilized seeds of corn (Zea mais L. Pioneer cv. PR32-B10) were hydroponically cultivated in a growth chamber under no-stressful conditions. The water-soluble protein extracts isolated from maize tissues showed peroxidase, polyphenol oxidase and catalase activities. Incubation of the extracts with naphthalene, fluorene, phenanthrene and pyrene, led to formation of oxidized and/or degradation products. GC-MS and TLC monitoring of the processes showed that naphthalene, phenanthrene, fluorene and pyrene underwent 100%, 78%, 92% and 65% oxidative degradation, respectively, after 120 min. The chemical structure of the degradation products were determined by (1)H NMR and ESI-MS spectrometry. PMID:27391049

  15. Polycyclovorans algicola gen. nov., sp. nov., an aromatic-hydrocarbon-degrading marine bacterium found associated with laboratory cultures of marine phytoplankton.

    Science.gov (United States)

    Gutierrez, Tony; Green, David H; Nichols, Peter D; Whitman, William B; Semple, Kirk T; Aitken, Michael D

    2013-01-01

    A strictly aerobic, halotolerant, rod-shaped bacterium, designated strain TG408, was isolated from a laboratory culture of the marine diatom Skeletonema costatum (CCAP1077/1C) by enrichment with polycyclic aromatic hydrocarbons (PAHs) as the sole carbon source. 16S rRNA gene sequence analysis placed this organism within the order Xanthomonadales of the class Gammaproteobacteria. Its closest relatives included representatives of the Hydrocarboniphaga-Nevskia-Sinobacter clade (<92% sequence similarity) in the family Sinobacteraceae. The strain exhibited a narrow nutritional spectrum, preferring to utilize aliphatic and aromatic hydrocarbon compounds and small organic acids. Notably, it displayed versatility in degrading two- and three-ring PAHs. Moreover, catechol 2,3-dioxygenase activity was detected in lysates, indicating that this strain utilizes the meta-cleavage pathway for aromatic compound degradation. Cells produced surface blebs and contained a single polar flagellum. The predominant isoprenoid quinone of strain TG408 was Q-8, and the dominant fatty acids were C(16:0), C(16:1) ω7c, and C(18:1) ω7c. The G+C content of the isolate's DNA was 64.3 mol% ± 0.34 mol%. On the basis of distinct phenotypic and genotypic characteristics, strain TG408 represents a novel genus and species in the class Gammaproteobacteria for which the name Polycyclovorans algicola gen. nov., sp. nov., is proposed. Quantitative PCR primers targeting the 16S rRNA gene of this strain were developed and used to show that this organism is found associated with other species of marine phytoplankton. Phytoplankton may be a natural biotope in the ocean where new species of hydrocarbon-degrading bacteria await discovery and which contribute significantly to natural remediation processes. PMID:23087039

  16. Plasmids and aromatic degradation in Sphingomonas for bioremediation : Aromatic ring cleavage genes in soil and rhizosphere

    OpenAIRE

    SipilÀ, Timo

    2009-01-01

    Microbial degradation pathways play a key role in the detoxification and the mineralization of polyaromatic hydrocarbons (PAHs), which are widespread pollutants in soil and constituents of petroleum hydrocarbons. In microbiology the aromatic degradation pathways are traditionally studied from single bacterial strains with capacity to degrade certain pollutant. In soil the degradation of aromatics is performed by a diverse community of micro-organisms. The aim of this thesis was to study biode...

  17. Degradation of polycyclic aromatic hydrocarbons (PAHs) in contaminated soils by Fenton's reagent: a multivariate evaluation of the importance of soil characteristics and PAH properties.

    Science.gov (United States)

    Jonsson, Sofia; Persson, Ylva; Frankki, Sofia; van Bavel, Bert; Lundstedt, Staffan; Haglund, Peter; Tysklind, Mats

    2007-10-01

    In this study, we investigated how the chemical degradability of polycyclic aromatic hydrocarbons (PAHs) in aged soil samples from various contaminated sites is influenced by soil characteristics and by PAH physico-chemical properties. The results were evaluated using the multivariate statistical tool, partial least squares projections to latent structures (PLS). The PAH-contaminated soil samples were characterised (by pH, conductivity, organic matter content, oxide content, particle size, specific surface area, and the time elapsed since the contamination events, i.e. age), and subjected to relatively mild, slurry-phase Fenton's reaction conditions. In general, low molecular weight PAHs were degraded to a greater extent than large, highly hydrophobic variants. Anthracene, benzo(a)pyrene, and pyrene were more susceptible to degradation than other, structurally similar, PAHs; an effect attributed to the known susceptibility of these compounds to reactions with hydroxyl radicals. The presence of organic matter and the specific surface area of the soil were clearly negatively correlated with the degradation of bi- and tri-cyclic PAHs, whereas the amount of degraded organic matter correlated positively with the degradation of PAHs with five or six fused rings. This was explained by enhanced availability of the larger PAHs, which were released from the organic matter as it degraded. Our study shows that sorption of PAHs is influenced by a combination of soil characteristics and physico-chemical properties of individual PAHs. Multivariate statistical tools have great potential for assessing the relative importance of these parameters.

  18. Biodegradation of Polycyclic Aromatic Hydrocarbons

    OpenAIRE

    DEMİR, İsmail; DEMİRBAĞ, Zihni

    1999-01-01

    Polycylic aromatic hydrocarbons (PAHs), such as petroleum and petroleum derivatives, are widespread organic pollutants entering the environment, chiefly, through oil spills and incomplete combustion of fossil fuels. Since most PAHs are persist in the environment for a long period of time and bioaccumulate, they cause environmental pollution and effect biological equilibrium dramatically. Biodegradation of some PAHs by microorganisms has been biochemically and genetically investigated. Ge...

  19. Strong Impact on the Polycyclic Aromatic Hydrocarbon (PAH)-Degrading Community of a PAH-Polluted Soil but Marginal Effect on PAH Degradation when Priming with Bioremediated Soil Dominated by Mycobacteria

    DEFF Research Database (Denmark)

    Johnsen, Anders R.; Schmidt, Stine; Hybholdt, Trine K.;

    2007-01-01

    Bioaugmentation of soil polluted with polycyclic aromatic hydrocarbons (PAHs) is often disappointing because of the low survival rate and low activity of the introduced degrader bacteria. We therefore investigated the possibility of priming PAH degradation in soil by adding 2% of bioremediated soil...... with a high capacity for PAH degradation. The culturable PAH-degrading community of the bioremediated primer soil was dominated by Mycobacterium spp. A microcosm containing pristine soil artificially polluted with PAHs and primed with bioremediated soil showed a fast, 100- to 1,000-fold increase in numbers...... of culturable phenanthrene-, pyrene-, and fluoranthene degraders and a 160-fold increase in copy numbers of the mycobacterial PAH dioxygenase gene pdo1. A nonpolluted microcosm primed with bioremediated soil showed a high rate of survival of the introduced degrader community during the 112 days of incubation...

  20. Accumulation and degradation of dead-end metabolites during treatment of soil contaminated with polycyclic aromatic hydrocarbons with five strains of white-rot fungi

    Energy Technology Data Exchange (ETDEWEB)

    Andersson, B.E. [Centre for Chemistry and Chemical Engineering, Dept. of Biotechnology, Lund Univ. (Sweden); Henrysson, T. [Centre for Chemistry and Chemical Engineering, Dept. of Biotechnology, Lund Univ. (Sweden)

    1996-12-31

    The white-rot fungi Trametes versicolor PRL 572, Trametes versicolor MUCL 28407, Pleurotus ostreatus MUCL 29527, Pleurotus sajor-caju MUCL 29757 and Phanerochaete chrysosporium DSM 1556 were investigated for their ability to degrade the polycyclic aromatic hydrocarbons (PAH) anthracene, benz[a]anthracene and dibenz[a, h]anthracene in soil. The fungi were grown on wheat straw and mixed with artificially contaminated soil. The results of this study show that, in a heterogeneous soil environment, the fungi have different abilities to degrade PAH, with Trametes showing little or no accumulation of dead-end metabolites and Phanerochaete and Pleurotus showing almost complete conversion of anthracene to 9,10-anthracenedione. In contrast to earlier studies, Phanerochaete showed the ability to degrade the accumulated 9,10-anthracenedione while Pleurotus did not. This proves that, in a heterogeneous soil system, the PAH degradation pattern for white-rot fungi can be quite different from that in a controlled liquid system. (orig.)

  1. 多环芳烃的微生物降解机制研究进展%Research Progress on Microbial Degradation Mechanisms for Polycyclic Aromatic Hydrocarbons

    Institute of Scientific and Technical Information of China (English)

    王涛; 蓝慧; 田云; 卢向阳

    2016-01-01

    多环芳烃是环境中最常见且最难降解的有机污染物之一。通过微生物降解使环境中的多环芳烃低毒化或无毒化是当今环境修复的研究热点之一。以萘和菲为研究对象,论述了多环芳烃的微生物降解机制,并阐述了生命组学新技术在多环芳烃降解机制研究中的应用,为深入探讨多环芳烃的微生物降解及转化机制奠定了理论基础。%Polycyclic aromatic hydrocarbons(PAHs)are one of the common and the most refractory organic pollutants in the environment.Nowadays,low-toxicity or non-toxicity of PAHs by microbial degradation is one of the research highlights in the field of environmental remediation.In this paper,using naphthalene and phe-nanthrene as example,the microbial degradation mechanisms of PAHs are reviewed,and the application of“omics”technology in life science for research of microbial degradation of PAHs is summarized.The review lays a certain theoretical foundation for further exploring the microbial degradation and conversion mechanism for PAHs.

  2. Deuterated polycyclic aromatic hydrocarbons: Revisited

    CERN Document Server

    Doney, Kirstin D; Mori, Tamami; Onaka, Takashi; Tielens, A G G M

    2016-01-01

    The amount of deuterium locked up in polycyclic aromatic hydrocarbons (PAHs) has to date been an uncertain value. We present a near-infrared (NIR) spectroscopic survey of HII regions in the Milky Way, Large Magellanic Cloud (LMC), and Small Magellanic Cloud (SMC) obtained with AKARI, which aims to search for features indicative of deuterated PAHs (PAD or Dn-PAH) to better constrain the D/H ratio of PAHs. Fifty-three HII regions were observed in the NIR (2.5-5 {\\mu}m), using the Infrared Camera (IRC) on board the AKARI satellite. Through comparison of the observed spectra with a theoretical model of deuterated PAH vibrational modes, the aromatic and (a)symmetric aliphatic C-D stretch modes were identified. We see emission features between 4.4-4.8 {\\mu}m, which could be unambiguously attributed to deuterated PAHs in only six of the observed sources, all of which are located in the Milky Way. In all cases, the aromatic C-D stretching feature is weaker than the aliphatic C-D stretching feature, and, in the case o...

  3. Biochemical ripening of dredged sediments. Part 2. Degradation of polycyclic aromatic hydrocarbons and total petroleum hydorcarbons in slurried and consolidated sediments

    NARCIS (Netherlands)

    Vermeulen, J.; Gool, van M.P.M.; Mentink, G.H.; Joziasse, J.; Bruning, H.; Grotenhuis, J.T.C.

    2007-01-01

    Ripening of polycyclic aromatic hydrocarbons (PAH) and total petroleum hydrocarbons (TPH) polluted dredged sediment can be considered as a bioremediation technique. Aerobic biodegradation of PAH and TPH was studied in five previously anaerobic-slurried sediments during a 350-d laboratory incubation

  4. Polycyclic aromatic hydrocarbons with SPICA

    CERN Document Server

    Berne, O; Mulas, G; Tielens, A G G M; Goicoechea, J R

    2009-01-01

    Thanks to high sensitivity and angular resolution and broad spectral coverage, SPICA will offer a unique opportunity to better characterize the nature of polycyclic aromatic hydrocarbons (PAHs) and very small grains (VSGs), to better use them as probes of astrophysical environments. The angular resolution will enable to probe the chemical frontiers in the evolution process from VSGs to neutral PAHs, to ionized PAHs and to "Grand-PAHs" in photodissotiation regions and HII regions, as a function of G$_0$/n (UV radiation field / density). High sensitivity will favor the detection of the far-IR skeletal emission bands of PAHs, which provide specific fingerprints and could lead to the identification of individual PAHs. This overall characterization will allow to use PAH and VSG populations as tracers of physical conditions in spatially resolved protoplanetary disks and nearby galaxies (using mid-IR instruments), and in high redshift galaxies (using the far-IR instrument), thanks to the broad spectral coverage SPIC...

  5. Birds and polycyclic aromatic hydrocarbons

    Science.gov (United States)

    Albers, P.H.

    2006-01-01

    Polycyclic aromatic hydrocarbons (PAH) are present throughout the global environment and are produced naturally and by activities of humans. Effects of PAH on birds have been determined by studies employing egg injection, egg immersion, egg shell application, single and multiple oral doses, subcutaneous injection, and chemical analysis of field-collected eggs and tissue. The four-to six-ring aromatic compounds are the most toxic to embryos, young birds, and adult birds. For embryos, effects include death, developmental abnormalities, and a variety of cellular and biochemical responses. For adult and young birds, effects include reduced egg production and hatching, increased clutch or brood abandonment, reduced growth, increased organweights, and a variety of biochemical responses. Trophic level accumulation is unlikely. Environmental exposure to PAH in areas of high human population or habitats affected by recent petroleum spills might be sufficient to adversely affect reproduction. Evidence of long-term effects of elevated concentrations of environmental PAH on bird populations is very limited and the mechanisms of effect are unclear.

  6. Degradation of Polycyclic Aromatic Hydrocarbons during Composting of Sewage Sludge%污泥堆腐过程中多环芳烃(PAHs)的降解

    Institute of Scientific and Technical Information of China (English)

    梁晶; 彭喜玲; 方海兰; 南蓬

    2011-01-01

    In the light of utilization of organic waste resource, a composting process of mixture of sewage sludge and greenery waste was carried out to study the degradation of polycyclic aromatic hydrocarbons (PAHs), which would provide clear evidence for the practice. Results indicated that total content of 16 priority PAHs in the maturation phase decreased to 3.202 mg/kg from the original 6.225 mg/kg, with degradation rate about 48.57%, and final PAHs content satisfied the accepted European Union cut-off limits for sludge to be considered safe for agricultural application set at 6 mg/kg. As far as an individual PAHs was concerned, PAHs containing fewer aromatic rings were easier to be degraded, which might be because the tendency of bioavailability of various PAH compounds during composting is strongly related to number of aromatic rings, molecular weight and sancture.%结合有机废弃物资源化利用的特点,进行了污泥与绿化植物废弃物堆肥实验,以探讨其中多环芳烃的降解状况,为其更好的资源化利用提供坚实的证据.研究表明,污泥与绿化植物废弃物物堆肥腐熟时,16种优控多环芳烃的总量由原来的6.225 mg/kg降到了3.202mg/kg,降解率达到了48.57%,并且堆肥后满足了欧洲联盟规定的多环芳烃农用限值6mg/kg.就单个多环芳烃化合物而言,环数越少降解效果越好,分析其原因可能与PAHs所含苯环多少以及其分子量大小有关.

  7. Volatilisation of aromatic hydrocarbons from soil

    DEFF Research Database (Denmark)

    Lindhardt, B.; Christensen, T.H.

    1996-01-01

    The non-steady-state fluxes of aromatic hydrocarbons were measured in the laboratory from the surface of soils contaminated with coal tar Four soil samples from a former gasworks site were used for the experiments. The fluxes were quantified for 11 selected compounds, 4 mono- and 7 polycyclic...... aromatic hydrocarbons, for a period of up to 8 or 16 days. The concentrations of the selected compounds in the soils were between 0.2 and 3,100 mu g/g. The study included the experimental determination of the distribution coefficient of the aromatic hydrocarbons between the sorbed phase and the water under...... saturated conditions. The determined distribution coefficients showed that the aromatic hydrocarbons were more strongly sorbed to the total organic carbon including the coal tar pitch - by a factor of 8 to 25 - than expected for natural organic matter. The fluxes were also estimated using an analytical...

  8. Bioremediation of multi-polluted soil by spent mushroom (Agaricus bisporus) substrate: Polycyclic aromatic hydrocarbons degradation and Pb availability.

    Science.gov (United States)

    García-Delgado, Carlos; Yunta, Felipe; Eymar, Enrique

    2015-12-30

    This study investigates the effect of three spent Agaricus bisporus substrate (SAS) application methods on bioremediation of soil multi-polluted with Pb and PAH from close to a shooting range with respect natural attenuation (SM). The remediation treatments involve (i) use of sterilized SAS to biostimulate the inherent soil microbiota (SSAS) and two bioaugmentation possibilities (ii) its use without previous treatment to inoculate A. bisporus and inherent microbiota (SAS) or (iii) SAS sterilization and further A. bisporus re-inoculation (Abisp). The efficiency of each bioremediation microcosm was evaluated by: fungal activity, heterotrophic and PAH-degrading bacterial population, PAH removal, Pb mobility and soil eco-toxicity. Biostimulation of the native soil microbiology (SSAS) achieved similar levels of PAH biodegradation as SM and poor soil detoxification. Bioaugmented microcosms produced higher PAH removal and eco-toxicity reduction via different routes. SAS increased the PAH-degrading bacterial population, but lowered fungal activity. Abisp was a good inoculum carrier for A. bisporus exhibiting high levels of ligninolytic activity, the total and PAH-degrading bacteria population increased with incubation time. The three SAS applications produced slight Pb mobilization (<0.3%). SAS sterilization and further A. bisporus re-inoculation (Abisp) proved the best application method to remove PAH, mainly BaP, and detoxify the multi-polluted soil. PMID:26188871

  9. Bioremediation of multi-polluted soil by spent mushroom (Agaricus bisporus) substrate: Polycyclic aromatic hydrocarbons degradation and Pb availability.

    Science.gov (United States)

    García-Delgado, Carlos; Yunta, Felipe; Eymar, Enrique

    2015-12-30

    This study investigates the effect of three spent Agaricus bisporus substrate (SAS) application methods on bioremediation of soil multi-polluted with Pb and PAH from close to a shooting range with respect natural attenuation (SM). The remediation treatments involve (i) use of sterilized SAS to biostimulate the inherent soil microbiota (SSAS) and two bioaugmentation possibilities (ii) its use without previous treatment to inoculate A. bisporus and inherent microbiota (SAS) or (iii) SAS sterilization and further A. bisporus re-inoculation (Abisp). The efficiency of each bioremediation microcosm was evaluated by: fungal activity, heterotrophic and PAH-degrading bacterial population, PAH removal, Pb mobility and soil eco-toxicity. Biostimulation of the native soil microbiology (SSAS) achieved similar levels of PAH biodegradation as SM and poor soil detoxification. Bioaugmented microcosms produced higher PAH removal and eco-toxicity reduction via different routes. SAS increased the PAH-degrading bacterial population, but lowered fungal activity. Abisp was a good inoculum carrier for A. bisporus exhibiting high levels of ligninolytic activity, the total and PAH-degrading bacteria population increased with incubation time. The three SAS applications produced slight Pb mobilization (soil.

  10. Partially oxidized polycyclic aromatic hydrocarbons show an increased bioavailability and biodegradability.

    NARCIS (Netherlands)

    Meulenberg, R.; Rijnaarts, H.H.M.; Doddema, H.J.; Field, J.A.

    1997-01-01

    Polycyclic aromatic hydrocarbons have a low water solubility and tend to adsorb on soil particles, which both result in slow bioremediation processes. Many microorganisms, known for their ability to degrade polycyclic aromatic hydrocarbons, only partially oxidize these compounds. White rot fungi, fo

  11. Environmental Remediation: Removal of polycyclic aromatic hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Nkansah, Marian Asantewah

    2012-11-15

    Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous persistent semi-volatile organic compounds. They are contaminants that are resistant to degradation and can remain in the environment for long periods due to their high degree of conjugation, and aromaticity. PAHs are present in industrial effluents as products of incomplete combustion processes of organic compounds. Petroleum, coal and shale oil contain extremely complex mixtures of these PAHs, and their transport and refining process can also result in the release of PAHs. It is therefore prudent that such effluents are treated before discharge into the environment. In this project, different approaches to the treatment of PAHs have been investigated. Hydrous pyrolysis has been explored as a potential technique for degrading PAHs in water using anthracene as a model compound. The experiments were performed under different conditions of temperature, substrate, redox systems and durations. The conditions include oxidising systems comprising pure water, hydrogen peroxide and Nafion-SiO2 solid catalyst in water; and reducing systems of formic acid and formic acid / Nafion-SiO2 / Pd-C catalysts to assess a range of reactivities. Products observed in GCMS analysis of the extract from the water phase include anthrone, anthraquinone, xanthone and multiple hydro-anthracene derivatives (Paper I). In addition a modified version of the Nafion-SiO2 solid catalyst in water oxidising system was tested; and reducing systems of formic acid and formic acid / Nafion-SiO2 / Pd-C catalysts were adopted for the conversion of a mixture of anthracene, fluorene and fluoranthene. The rate of conversion in the mixture was high as compared to that of only anthracene (Paper II). Also the use of LECA (Lightweight expanded clay aggregates) as an adsorbent (Paper III) for PAHs (phenanthrene, fluoranthene and pyrene) removal from water has been.(Author)

  12. Croceicoccus naphthovorans sp. nov., a polycyclic aromatic hydrocarbons-degrading and acylhomoserine-lactone-producing bacterium isolated from marine biofilm, and emended description of the genus Croceicoccus.

    Science.gov (United States)

    Huang, Yili; Zeng, Yanhua; Feng, Hao; Wu, Yuehong; Xu, Xuewei

    2015-05-01

    A polycyclic aromatic hydrocarbons-degrading and acylhomoserine-lactone-producing marine bacterium, designated strain PQ-2(T), was isolated from marine biofilm collected from a boat shell at a harbour of Zhoushan island in Zhejiang Province, PR China. Strain PQ-2(T) is Gram-stain-negative, yellow-pigmented, non-motile and short rod-shaped. Optimal growth of strain PQ-2(T) was observed at 32 °C, at pH 7.0 and in 2% (w/v) NaCl. The 16S rRNA gene sequence of strain PQ-2(T) showed highest similarity to Croceicoccus marinus E4A9(T) (96.3%) followed by Novosphingobium malaysiense MUSC 273(T) (95.6%) and Altererythrobacter marinus H32(T) (95.6%). Phylogenetic analysis with all species of the family Erythrobacteraceae with validly published names revealed that strain PQ-2(T) formed a phyletic line with Croceicoccus marinus E4A9(T) that was distinct from other members of the family Erythrobacteraceae . The sole respiratory quinone was ubiquinone 10 (Q-10). The predominant fatty acids were C18 : 1ω7c, C17 : 1ω6c and summed feature 3 (C16 : 1ω7c and/or iso-C15 : 0 2-OH). The genomic DNA G+C content was 61.7 mol%. In the polar lipid profile, phosphatidylethanolamine, phosphatidylcholine, phosphatidylglycerol, one unidentified phospholipid and one sphingoglycolipid were the major compounds; and another sphingoglycolipid was present in a minor amount. Based on the genotypic and phenotypic data, strain PQ-2(T) represents a novel species of the genus Croceicoccus , for which the name Croceicoccus naphthovorans sp. nov. is proposed. The type strain is PQ-2(T) ( =CGMCC 1.12805(T) =NBRC 110381(T)). In addition, emended descriptions for the genus Croceicoccus and the species C. marinus are given. PMID:25713040

  13. In situ biodegradation potential of aromatic hydrocarbons in anaerobic groundwaters

    Science.gov (United States)

    Acton, D. W.; Barker, J. F.

    1992-04-01

    Three types of experiments were conducted to assess the potential for enhancing the in situ biodegradation of nine aromatic hydrocarbons in anaerobic, leachate-impacted aquifers at North Bay, Ontario, and at Canada Forces Base Borden. Laboratory micrososms containing authentic aquifer material and groundwater from the North Bay site were amended with nitrate and glucose. No significant losses of aromatic hydrocarbons were observed compared to unamended controls, over a period of 187 days. A total of eight in situ biodegradation columns were installed in the North Bay and Borden aquifers. Remedial additions included electron acceptors (nitrate and sulphate) and primary substrates (acetate, lactate and yeast extract). Six aromatic hydrocarbons [toluene, ethylbenzene, m-xylene, o-xylene, cumene and 1,2,4-trimethylbenzene ( 1,2,4-TMB)] were completely degraded in at least one in situ column at the North Bay site. Only toluene was degraded in the Borden aquifer. In all cases, aromatic hydrocarbon attenuation was attributed to biodegradation by methanogenic and fermentative bacteria. No evidence of aromatic hydrocarbon degradation was observed in columns remediated with nitrate or primary substrates. A continuous forced gradient injection experiment with sulphate addition was conducted at the North Bay site over a period of 51 days. The concentration of six aromatic hydrocarbons was monitored over time in the injection wells and at piezometer fences located 2, 5 and 10 m downgradient. All compounds except toluene reached injection concentration between 14 and 26 days after pumping began, and showed some evidence of selective retardation. Toluene broke through at a subdued concentration (˜ 50% of injection levels), and eventually declined to undetectable levels on day 43. This attenuation was attributed to adaptation and biodegradation by anaerobic bacteria. The results from these experiments indicate that considerable anaerobic biodegradation of aromatic hydrocarbons in

  14. Bacterial degradation of monocyclic aromatic amines

    Directory of Open Access Journals (Sweden)

    Pankaj Kumar Arora

    2015-08-01

    Full Text Available Aromatic amines are an important group of industrial chemicals, which are widely used for manufacturing of dyes, pesticides, drugs, pigments, and other industrial products. These compounds have been considered highly toxic to human beings due to their carcinogenic nature. Three groups of aromatic amines have been recognized: monocyclic, polycyclic and heterocyclic aromatic amines. Bacterial degradation of several monocyclic aromatic compounds has been studied in a variety of bacteria, which utilizes monocyclic aromatic amines as their sole source of carbon and energy. Several degradation pathways have been proposed and the related enzymes and genes have also been characterized. Many reviews have been reviewed toxicity of monocyclic aromatic amines; however, there is lack of review on biodegradation of monocyclic aromatic amines. The aim of this review is to summarize bacterial degradation of monocyclic aromatic amines. This review will increase our current understanding of biochemical and molecular basis of bacterial degradation of monocyclic aromatic amines.

  15. Anaerobic degradation of aromatic hydrocarbons

    International Nuclear Information System (INIS)

    This paper reports that toluene and m-xylene were rapidly mineralized in a denitrifying laboratory aquifer column operated under continuous flow conditions in the complete absence of molecular oxygen. A bacterium, tentatively identified as a Pseudomonas sp., was isolated from this column. This organism mineralized toluene and m-xylene under pure culture conditions with nitrate or nitrous oxide as the sole electron acceptors. Carbon balance studies using 0.3mM [ring-UL-14C]toluene revealed that more than 50 percent of the radioactivity was evolved as 14CO2

  16. Dihydrodiol dehydrogenase and polycyclic aromatic hydrocarbon metabolism

    Energy Technology Data Exchange (ETDEWEB)

    Smithgall, T.E.

    1986-01-01

    Carcinogenic activation of polycyclic aromatic hydrocarbons by microsomal monoxygenases proceeds through trans-dihydrodiol metabolites to diol-epoxide ultimate carcinogens. This thesis directly investigated the role of dihydrodiol dehydrogenase, a cytosolic NAD(P)-linked oxidoreductase, in the detoxification of polycyclic aromatic trans-dihydrodiols. A wide variety of non-K-region trans-dihydrodiols were synthesized and shown to be substrates for the homogeneous rat liver dehydrogenase, including several potent proximate carcinogens derived from 7,12-dimethylbenz(a)anthracene, 5-methylchrysene, and benzo(a)pyrene. Since microsomal activation of polycyclic aromatic hydrocarbons is highly stereospecific, the stereochemical course of enzymatic trans-dihydrodiol oxidation was monitored using circular dichroism spectropolarimetry. The major product formed from the dehydrogenase-catalyzed oxidation of the trans-1,2-dihydrodiol of naphthalene was characterized using UV, IR, NMR, and mass spectroscopy, and appears to be 4-hydroxy-1,2-naphthoquinone. Mass spectral analysis suggests that an analogous hydroxylated o-quinone is formed as the major product of benzo(a)pyrene-7,8-dihydrodiol oxidation. Enzymatic oxidation of trans-dihydrodiols was shown to be potently inhibited by all of the major classes of the nonsteroidal antiinflammatory drugs. Enhancement of trans-dihydrodiol proximate carcinogen oxidation may protect against possible adverse effects of the aspirin-like drugs, and help maintain the balance between activation and detoxification of polycyclic aromatic hydrocarbons.

  17. HYDROCARBON-DEGRADING BACTERIA AND SURFACTANT ACTIVITY

    Energy Technology Data Exchange (ETDEWEB)

    Brigmon, R; Topher Berry, T; Grazyna A. Plaza, G; jacek Wypych, j

    2006-08-15

    Fate of benzene ethylbenzene toluene xylenes (BTEX) compounds through biodegradation was investigated using two different bacteria, Ralstonia picketti (BP-20) and Alcaligenes piechaudii (CZOR L-1B). These bacteria were isolated from extremely polluted petroleum hydrocarbon contaminated soils. PCR and Fatty Acid Methyl Ester (FAME) were used to identify the isolates. Biodegradation was measured using each organism individually and in combination. Both bacteria were shown to degrade each of the BTEX compounds. Alcaligenes piechaudii biodegraded BTEXs more efficiently while mixed with BP-20 and individually. Biosurfactant production was observed by culture techniques. In addition 3-hydroxy fatty acids, important in biosurfactant production, was observed by FAME analysis. In the all experiments toluene and m+p- xylenes were better growth substrates for both bacteria than the other BTEX compounds. In addition, the test results indicate that the bacteria could contribute to bioremediation of aromatic hydrocarbons (BTEX) pollution increase biodegradation through the action by biosurfactants.

  18. Molecular application for identification of polycyclic aromatic hydrocarbons degrading bacteria (PAHD) species isolated from oil polluted soil in Dammam, Saud Arabia.

    Science.gov (United States)

    Ibrahim, Mohamed M; Al-Turki, Ameena; Al-Sewedi, Dona; Arif, Ibrahim A; El-Gaaly, Gehan A

    2015-09-01

    Soil contamination with petroleum hydrocarbon products such as diesel and engine oil is becoming one of the major environmental problems. This study describes hydrocarbons degrading bacteria (PHAD) isolated from long-standing petrol polluted soil from the eastern region, Dammam, Saudi Arabia. The isolated strains were firstly categorized by accessible shape detection, physiological and biochemistry tests. Thereafter, a technique established on the sequence analysis of a 16S rDNA gene was used. Isolation of DNA from the bacterial strains was performed, on which the PCR reaction was carried out. Strains were identified based on 16S rDNA sequence analysis, As follows amplified samples were spontaneously sequenced automatically and the attained results were matched to open databases. Among the isolated bacterial strains, S1 was identified as Staphylococcus aureus and strain S1 as Corynebacterium amycolatum. PMID:26288572

  19. Calculated molecular properties of polycyclic aromatic hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Hites, R.A.; Simonsick, W.J. Jr.

    1987-01-01

    This volume contains a compilation of calculated molecular properties for 272 polycyclic aromatic hydrocarbons (PAH) and monomethylated PAH, listed in sequence according to their increasing molecular weight. The Chemical Abstracts Registry number is also included for easy reference. The molecular properties were calculated using the semiempirical MDCO method with geometric optimization. These parameters include the heats of formation, the frontier orbital energies, the electronic and nuclear energies, the dipole moment, and the net atomic charges on each atom. The shape parameter and the length/breadth ratio from the optimized geometries is also computed.

  20. Removal of high-molecular weight polycyclic aromatic hydrocarbons

    Directory of Open Access Journals (Sweden)

    Ulrich Vasconcelos

    2011-01-01

    Full Text Available Alternatives for the removal of high-molecular weight polycyclic aromatic hydrocarbons (HWM-PAH from soil were tested by adding fertilizer or glycerol, as well as the combination of both. Experiments were carried out for 60 days in reactors containing a HWM-PAH-contaminated soil (8030 μg kg-1, accompanied by pH monitoring, humidity control and quantification of total heterotrophic bacteria and total fungus. Fertilizer addition removed 41.6% of HWM-PAH. Fertilizer and glycerol in combination removed 46.2%. When glycerol was added individually, degradation reached 50.4%. Glycerol also promoted the increase of degradation rate during the first 30 days suggesting the HMW-PAH removal occurred through cometabolic pathways.

  1. Modeling the fate of polynuclear aromatic hydrocarbons in the rhizosphere

    International Nuclear Information System (INIS)

    Polynuclear aromatic hydrocarbons (PAHs) are major contaminants associated with wastes from manufactured gas plants, wood treating operations, and petroleum refining; they are potentially carcinogenic and mutagenic. It has been known that vegetation can enhance the rate and extent of degradation of PAHs in contaminated soil. Plant roots release exudates capable of supplying carbon and energy to microflora for degrading PAHs. It has also been well established that the population of microorganisms in the rhizosphere is significantly greater than that in the non-vegetated soil; these microorganisms are apparently responsible for the enhanced biodegradation of PAHs. A model has been derived for describing the rate of disappearance of a non-aqueous phase contaminant in the rhizosphere, which takes into account dissolution, adsorption, desorption and biodegradation of the contaminant, without neglecting the size distribution of the organic-phase droplets; the rate of biodegradation is expressed in terms of the Monod kinetics. The model is validated with the available experimental data for pyrene

  2. Structural Evolution of Interstellar Polycyclic Aromatic Hydrocarbons

    Science.gov (United States)

    Hammonds, Mark; Candian, Alessandra; Mori, Tamami; Usui, Fumihiko; Onaka, Takashi

    2015-08-01

    Polycyclic Aromatic Hydrocarbons (PAHs) are an important reservoir for molecular carbon in the interstellar medium (ISM), and investigations into their chemistry and behaviour may be important to the understanding of how carbon is processed from simple forms into complex prebiotic molecules such as those detected in chondritic meteorites. In this study, infrared astronomical data from AKARI and other observatories are used together with laboratory and theoretical data to study variations in the structure of emitting PAHs in interstellar environments using spectroscopic decomposition techniques and bands arising from carbon-hydrogen bond vibrations at wavelengths from 3 - 14 microns. Results and inferences are discussed in terms of the processing of large carbonaceous molecules in astrophysical environments.

  3. Polycyclic aromatic hydrocarbons (PAHs) in yogurt samples.

    Science.gov (United States)

    Battisti, Chiara; Girelli, Anna Maria; Tarola, Anna Maria

    2015-01-01

    The concentrations and distributions of major polycyclic aromatic hydrocarbons (PAHs) were determined in 20 kinds of yogurt specimens collected from Italian supermarkets using reversed phase high-performance liquid chromatography equipped with fluorescence detection. The method was validated by determination of recovery percentages, precision (repeatability) and sensitivity (limits of detection) with yogurt samples fortified at 0.25, 0.5 and 1 µg/kg concentration levels. The recovery of 13 PAHs, with the exception of naphthalene and acenaphthene, ranged from 61% to 130% and from 60% to 97% at all the levels for yogurts with low (0.1%) and high (3.9%) fat content, respectively. The method is repeatable with relative standard deviation values yogurts with low and high fats were compared.

  4. Degradation of hydrocarbons under methanogenic conditions in different geosystems

    Science.gov (United States)

    Straaten, Nontje; Jiménez García, Núria; Richnow, Hans-Hermann; Krueger, Martin

    2014-05-01

    With increasing energy demand the search for new resources is becoming increasingly important for the future energy supply. Therefore the knowledge about fossil fuels like oil or natural gas and their extraction should be expanded. Biodegraded oil is found in many reservoirs worldwide. Consequently, it is very important to get insight in the microbial communities and metabolic processes involved in hydrocarbon degradation. Due to the lack of alternative electron acceptors in hydrocarbon-rich geosystems, degradation often takes place under methanogenic conditions. The aim of the present study is to identify the microorganisms and mechanisms involved in the degradation of complex hydrocarbons, like BTEX and polycyclic aromatic hydrocarbons, using culture dependent and independent techniques. For this purpose enrichment cultures from marine sediments, shales, coal and oil reservoirs are monitored for their capability to degrade alkanes and aromatic compounds. Moreover the environmental samples of these different geosystems analysed for evidence for the in situ occurrence of methanogenic oil degradation. The gas geochemical data provided in several cases hints for a recent biological origin of the methane present. First results of the microbial community analysis showed in environmental samples and enrichment cultures the existence of Bacteria known to degrade hydrocarbons. Also a diverse community of methanogenic Archaea could be found in the clone libraries. Additionally, in oil and coal reservoir samples the degradation of model hydrocarbons, e.g. methylnaphthalene, hexadecane and BTEX, to CH4 was confirmed by 13C-labeling. To explore the mechanisms involved in biodegradation, the enrichments as well as the original environmental samples are further analysed for the presence of respective functional genes.

  5. Reconstructing metabolic pathways of hydrocarbon-degrading bacteria from the Deepwater Horizon oil spill.

    Science.gov (United States)

    Dombrowski, Nina; Donaho, John A; Gutierrez, Tony; Seitz, Kiley W; Teske, Andreas P; Baker, Brett J

    2016-01-01

    The Deepwater Horizon blowout in the Gulf of Mexico in 2010, one of the largest marine oil spills(1), changed bacterial communities in the water column and sediment as they responded to complex hydrocarbon mixtures(2-4). Shifts in community composition have been correlated to the microbial degradation and use of hydrocarbons(2,5,6), but the full genetic potential and taxon-specific metabolisms of bacterial hydrocarbon degraders remain unresolved. Here, we have reconstructed draft genomes of marine bacteria enriched from sea surface and deep plume waters of the spill that assimilate alkane and polycyclic aromatic hydrocarbons during stable-isotope probing experiments, and we identify genes of hydrocarbon degradation pathways. Alkane degradation genes were ubiquitous in the assembled genomes. Marinobacter was enriched with n-hexadecane, and uncultured Alpha- and Gammaproteobacteria populations were enriched in the polycyclic-aromatic-hydrocarbon-degrading communities and contained a broad gene set for degrading phenanthrene and naphthalene. The repertoire of polycyclic aromatic hydrocarbon use varied among different bacterial taxa and the combined capabilities of the microbial community exceeded those of its individual components, indicating that the degradation of complex hydrocarbon mixtures requires the non-redundant capabilities of a complex oil-degrading community. PMID:27572965

  6. High atmosphere-ocean exchange of semivolatile aromatic hydrocarbons

    Science.gov (United States)

    González-Gaya, Belén; Fernández-Pinos, María-Carmen; Morales, Laura; Méjanelle, Laurence; Abad, Esteban; Piña, Benjamin; Duarte, Carlos M.; Jiménez, Begoña; Dachs, Jordi

    2016-06-01

    Polycyclic aromatic hydrocarbons, and other semivolatile aromatic-like compounds, are an important and ubiquitous fraction of organic matter in the environment. The occurrence of semivolatile aromatic hydrocarbons is due to anthropogenic sources such as incomplete combustion of fossil fuels or oil spills, and other biogenic sources. However, their global transport, fate and relevance for the carbon cycle have been poorly assessed, especially in terms of fluxes. Here we report a global assessment of the occurrence and atmosphere-ocean fluxes of 64 polycyclic aromatic hydrocarbons analysed in paired atmospheric and seawater samples from the tropical and subtropical Atlantic, Pacific and Indian oceans. The global atmospheric input of polycyclic aromatic hydrocarbons to the global ocean is estimated at 0.09 Tg per month, four times greater than the input from the Deepwater Horizon spill. Moreover, the environmental concentrations of total semivolatile aromatic-like compounds were 102-103 times higher than those of the targeted polycyclic aromatic hydrocarbons, with a relevant contribution of an aromatic unresolved complex mixture. These concentrations drive a large global deposition of carbon, estimated at 400 Tg C yr-1, around 15% of the oceanic CO2 uptake.

  7. High atmosphere–ocean exchange of semivolatile aromatic hydrocarbons

    KAUST Repository

    González-Gaya, Belén

    2016-05-16

    Polycyclic aromatic hydrocarbons, and other semivolatile aromatic-like compounds, are an important and ubiquitous fraction of organic matter in the environment. The occurrence of semivolatile aromatic hydrocarbons is due to anthropogenic sources such as incomplete combustion of fossil fuels or oil spills, and other biogenic sources. However, their global transport, fate and relevance for the carbon cycle have been poorly assessed, especially in terms of fluxes. Here we report a global assessment of the occurrence and atmosphere-ocean fluxes of 64 polycyclic aromatic hydrocarbons analysed in paired atmospheric and seawater samples from the tropical and subtropical Atlantic, Pacific and Indian oceans. The global atmospheric input of polycyclic aromatic hydrocarbons to the global ocean is estimated at 0.09 Tg per month, four times greater than the input from the Deepwater Horizon spill. Moreover, the environmental concentrations of total semivolatile aromatic-like compounds were 10 2 -10 3 times higher than those of the targeted polycyclic aromatic hydrocarbons, with a relevant contribution of an aromatic unresolved complex mixture. These concentrations drive a large global deposition of carbon, estimated at 400 Tg C yr -1, around 15% of the oceanic CO2 uptake. © 2016 Macmillan Publishers Limited.

  8. Selection of ionic liquids for the extraction of aromatic hydrocarbons from aromatic/aliphatic mixtures

    NARCIS (Netherlands)

    Meindersma, G. Wytze; Podt, Anita (J.G.); Haan, de André B.

    2005-01-01

    The separation of aromatic hydrocarbons (benzene, toluene, ethyl benzene and xylenes) from C4 to C10 aliphatic hydrocarbon mixtures is challenging since these hydrocarbons have boiling points in a close range and several combinations form azeotropes. In this work, we investigated the separation of t

  9. Biodegradation of polycyclic aromatic hydrocarbons by arbuscular mycorrhizal leek plants

    Energy Technology Data Exchange (ETDEWEB)

    Liu, A.; Dalpe, Y. [Agriculture Canada, Ottawa, ON (Canada). Grain and Oilseeds Branch

    2005-07-01

    A study was conducted to examine the response of arbuscular mycorrhizal fungi (AMF) on the degradation of polycyclic aromatic hydrocarbon (PAH), nutrient uptake, and leek growth under greenhouse conditions. This experiment included 3 mycorrhizal treatments, 2 microorganism treatments, 2 PAH chemicals, and 4 concentrations of PAHs. Plant growth was greatly reduced by the addition of anthracene or phenanthrene in soil, whereas mycorrhizal inoculation not only increased plant growth, but also enhanced uptake of nitrogen and phosphorus. PAH concentrations in soil was lowered through the inoculation of two different strains of the species G. intraradices and G. versiforme. In 12 weeks of pot cultures, anthracene and phenanthrene concentrations decreased for all 3 PAH levels tested. However, the reduced amount of phenanthrene in soil was greater than that of anthracene. The addition of a soil microorganism extract into pot cultures accelerated the PAH degradation. The inoculation of AMF in a hydrocarbon contaminated soil was shown to enhance PAHs soil decontamination. It was concluded that a soil colonized with AMF can not only improve plant growth but can also stimulate soil microflora abundance and diversity. AMF may therefore directly influence PAH soil decontamination through plant growth enhancement.

  10. Porphyrins Fused with Unactivated Polycyclic Aromatic Hydrocarbons

    KAUST Repository

    Diev, Vyacheslav V.

    2012-01-06

    A systematic study of the preparation of porphyrins with extended conjugation by meso,β-fusion with polycyclic aromatic hydrocarbons (PAHs) is reported. The meso-positions of 5,15-unsubstituted porphyrins were readily functionalized with PAHs. Ring fusion using standard Scholl reaction conditions (FeCl 3, dichloromethane) occurs for perylene-substituted porphyrins to give a porphyrin β,meso annulated with perylene rings (0.7:1 ratio of syn and anti isomers). The naphthalene, pyrene, and coronene derivatives do not react under Scholl conditions but are fused using thermal cyclodehydrogenation at high temperatures, giving mixtures of syn and anti isomers of the meso,β-fused porphyrins. For pyrenyl-substituted porphyrins, a thermal method gives synthetically acceptable yields (>30%). Absorption spectra of the fused porphyrins undergo a progressive bathochromic shift in a series of naphthyl (λ max = 730 nm), coronenyl (λ max = 780 nm), pyrenyl (λ max = 815 nm), and perylenyl (λ max = 900 nm) annulated porphyrins. Despite being conjugated with unsubstituted fused PAHs, the β,meso-fused porphyrins are more soluble and processable than the parent nonfused precursors. Pyrenyl-fused porphyrins exhibit strong fluorescence in the near-infrared (NIR) spectral region, with a progressive improvement in luminescent efficiency (up to 13% with λ max = 829 nm) with increasing degree of fusion. Fused pyrenyl-porphyrins have been used as broadband absorption donor materials in photovoltaic cells, leading to devices that show comparatively high photovoltaic efficiencies. © 2011 American Chemical Society.

  11. Theory and application of landfarming to remediate polycyclic aromatic hydrocarbons and mineral oil-contaminated sediments: beneficial reuse

    NARCIS (Netherlands)

    Harmsen, J.; Rulkens, W.H.; Sims, R.C.; Rijtema, P.E.; Zweers, A.J.

    2007-01-01

    When applying landfarming for the remediation of contaminated soil and sediment, a fraction of the soil-bound contaminant is rapidly degraded; however, a residual concentration may remain, which slowly degrades. Degradation of polycyclic aromatic hydrocarbons (PAHs) and mineral oil can be described

  12. Polycyclic aromatic hydrocarbons and nitropolycyclic aromatic hydrocarbons in particulates emitted by motorcycles

    International Nuclear Information System (INIS)

    We determined eleven PAHs and four NPAHs in particulates and regulated pollutants (CO, CO2, HC, NOx, PM) exhausted from motorcycles to figure out the characteristics of motorcycle exhausts. Fluoranthene and pyrene accounted for more than 50% of the total detected PAHs. Among four detected NPAHs, 6-nitrochrysene and 7-nitrobenz[a]anthracene were the predominant NPAHs and were highly correlated relationship with their parent PAHs (R = 0.93 and 0.97, respectively). The PM and HC emissions tended to be close to the PAH emissions. NOx and NPAHs were negatively correlated. Despite their small engine size, motorcycles emitted much more PM and PAHs, showed stronger PAH-related carcinogenicity and indirect-acting mutagenicity, but weaker NPAH-related direct-acting mutagenic potency than automobiles. This is the first study to analyze both PAHs and NPAHs emitted by motorcycles, which could provide useful information to design the emission regulations and standards for motorcycles such as PM. -- Highlights: ► We characterized PAHs and NPAHs distribution in motorcycle exhausts. ► NPAHs concentrations were about three orders of magnitude lower than those of PAHs. ► We found larger amounts of PM and PAHs in exhaust of motorcycles than of automobiles. ► Motorcycles showed stronger PAH-related toxicity than automobiles. ► Motorcycles showed weaker NPAH-related direct-acting mutagenicity than automobiles. -- Control polycyclic aromatic hydrocarbons and nitropolycyclic aromatic hydrocarbon in particulates emitted by motorcycles due to their toxic potency

  13. Polycyclic aromatic hydrocarbon emissions from motorcycles

    Science.gov (United States)

    Yang, Hsi-Hsien; Hsieh, Lien-Te; Liu, Hsu-Chung; Mi, Hsiao-Hsuan

    Emissions of polycyclic aromatic hydrocarbons (PAHs, 2-7 ring) and regulated air pollutants (CO, HC, NO x, PM) from 2-stroke carburetor (2-Stk/Cb), 4-stroke carburetor (4-Stk/Cb) and 4-stroke fuel injection (4-Stk/FI) motorcycles were investigated by testing these vehicles on a chassis dynamometer. Exhaust samplings were carried out on diluted exhausts in a dilution tunnel connected to a constant volume sampling system. Measurements were performed on a standard driving cycle. The results reveal that low molecular weight PAHs (especially naphthalene) dominated in the exhaust gas. The averages of soluble organic fractions were 86.4%, 46.3% and 48.9% for the 2-Stk/Cb, 4-Stk/Cb and 4-Stk/FI motorcycles, respectively. PAH emissions are greater from cold-start driving than those from hot-start driving cycle for all these three kinds of motorcycles. Total PAH emission factors were 8320, 5990 and 3390 μg km -1 for the in-used 2-Stk/Cb, 4-Stk/Cb and 4-Stk/FI motorcycles, respectively. PAH emission factors were the largest for the 2-Stk/Cb motorcycles. Besides, the 2-Stk/Cb motorcycle had the largest total BaP equivalent emission factor of 10.8 μg km -1, indicating that the emission exhaust from the 2-Stk/Cb motorcycle was most carcinogenic. HC, PM and PAH emissions were the lowest for the 4-Stk/FI motorcycles. The correlation coefficient between CO and total PAH emissions for all the test motorcycles was 0.51, indicating that CO and PAH emissions are not highly correlated.

  14. Partition of polycyclic aromatic hydrocarbons on organobentonites

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    A series of organobentonites synthesized by exchanging organiccation such as dodecyltri-methylammonium (DTMA),benzyldimethyltetradecylammonium (BDTDA), cetyltrimethyl-ammonium (CTMA), octodeyltrimethylammonium (OTMA) on bentonite. The optimal condition, properties and mechanisms for the organobentonites to sorb phenanthrene, anthracene, naphthalene, acenaphthene in water were investigated in detail. The partition behavior was determined for four polycyclic aromatic hydrocarbons (PAHs), such as naphthalene, phenanthrene, anthracene and acenaphthene, from water to a series of organobentonites. The interlayer spacings and organic carbon contents of organobentonites, removal rate and sorption capacities for organobentonites to treat phenanthrene,anthracene, naphthalene, acenaphthene were correlated to the length of alkyl chains and the amounts of cation surfactant exchanged on Foundation item: the bentonite. Phenanthrene, anthracene, naphthalene, and acenaphthene sorption to organobentonites were characterized by linear isotherms, indicating solute partition between water and the organic phase composed of the large alkyl functional groups of quaternary ammonium cations. PAHs distribution coefficients (Kd)between organobentonites and water were proportional to the organic carbon contents of organobentonites. However, the partition coefficients (Koc) were nearly constants for PAHs in the system of organobentonite-water. The Koc of phenanthrene, anthracene,naphthalene, acenaphthene were 2.621x105, 2.106x105, 2.247x104,5.085x104, respectively. The means Koc values on the organobentonites are about ten to twenty times larger than the values on the soils/sediments, what is significant prerequisite for organobentonite to apply to remediation of pollution soil and groundwater. The sorption mechanism was also evaluated from octanol-water partition coefficients and aqueous solubility of PAHs. The correlations between lgKoc and 1gkow, 1gKoc and 1gS for PAHs in the system of water

  15. Biodegradation aspects of Polycyclic Aromatic Hydrocarbons (PAHs): A review

    Energy Technology Data Exchange (ETDEWEB)

    Haritash, A.K., E-mail: akharitash@gmail.com [Department of Environmental Science and Engineering, Guru Jambheshwar University of Science and Technology, Hisar, Haryana (India); Kaushik, C.P. [Department of Environmental Science and Engineering, Guru Jambheshwar University of Science and Technology, Hisar, Haryana (India)

    2009-09-30

    PAHs are aromatic hydrocarbons with two or more fused benzene rings with natural as well as anthropogenic sources. They are widely distributed environmental contaminants that have detrimental biological effects, toxicity, mutagenecity and carcinogenicity. Due to their ubiquitous occurrence, recalcitrance, bioaccumulation potential and carcinogenic activity, the PAHs have gathered significant environmental concern. Although PAH may undergo adsorption, volatilization, photolysis, and chemical degradation, microbial degradation is the major degradation process. PAH degradation depends on the environmental conditions, number and type of the microorganisms, nature and chemical structure of the chemical compound being degraded. They are biodegraded/biotransformed into less complex metabolites, and through mineralization into inorganic minerals, H{sub 2}O, CO{sub 2} (aerobic) or CH{sub 4} (anaerobic) and rate of biodegradation depends on pH, temperature, oxygen, microbial population, degree of acclimation, accessibility of nutrients, chemical structure of the compound, cellular transport properties, and chemical partitioning in growth medium. A number of bacterial species are known to degrade PAHs and most of them are isolated from contaminated soil or sediments. Pseudomonas aeruginosa, Pseudomons fluoresens, Mycobacterium spp., Haemophilus spp., Rhodococcus spp., Paenibacillus spp. are some of the commonly studied PAH-degrading bacteria. Lignolytic fungi too have the property of PAH degradation. Phanerochaete chrysosporium, Bjerkandera adusta, and Pleurotus ostreatus are the common PAH-degrading fungi. Enzymes involved in the degradation of PAHs are oxygenase, dehydrogenase and lignolytic enzymes. Fungal lignolytic enzymes are lignin peroxidase, laccase, and manganese peroxidase. They are extracellular and catalyze radical formation by oxidation to destabilize bonds in a molecule. The biodegradation of PAHs has been observed under both aerobic and anaerobic conditions

  16. Biodegradation aspects of Polycyclic Aromatic Hydrocarbons (PAHs): A review

    International Nuclear Information System (INIS)

    PAHs are aromatic hydrocarbons with two or more fused benzene rings with natural as well as anthropogenic sources. They are widely distributed environmental contaminants that have detrimental biological effects, toxicity, mutagenecity and carcinogenicity. Due to their ubiquitous occurrence, recalcitrance, bioaccumulation potential and carcinogenic activity, the PAHs have gathered significant environmental concern. Although PAH may undergo adsorption, volatilization, photolysis, and chemical degradation, microbial degradation is the major degradation process. PAH degradation depends on the environmental conditions, number and type of the microorganisms, nature and chemical structure of the chemical compound being degraded. They are biodegraded/biotransformed into less complex metabolites, and through mineralization into inorganic minerals, H2O, CO2 (aerobic) or CH4 (anaerobic) and rate of biodegradation depends on pH, temperature, oxygen, microbial population, degree of acclimation, accessibility of nutrients, chemical structure of the compound, cellular transport properties, and chemical partitioning in growth medium. A number of bacterial species are known to degrade PAHs and most of them are isolated from contaminated soil or sediments. Pseudomonas aeruginosa, Pseudomons fluoresens, Mycobacterium spp., Haemophilus spp., Rhodococcus spp., Paenibacillus spp. are some of the commonly studied PAH-degrading bacteria. Lignolytic fungi too have the property of PAH degradation. Phanerochaete chrysosporium, Bjerkandera adusta, and Pleurotus ostreatus are the common PAH-degrading fungi. Enzymes involved in the degradation of PAHs are oxygenase, dehydrogenase and lignolytic enzymes. Fungal lignolytic enzymes are lignin peroxidase, laccase, and manganese peroxidase. They are extracellular and catalyze radical formation by oxidation to destabilize bonds in a molecule. The biodegradation of PAHs has been observed under both aerobic and anaerobic conditions and the rate can be

  17. Sorption of polycyclic aromatic hydrocarbons to polystyrene nanoplastic.

    Science.gov (United States)

    Liu, Lijing; Fokkink, Remco; Koelmans, Albert A

    2016-07-01

    Microplastic has become an emerging contaminant of global concern. Bulk plastic can degrade to form smaller particles down to the nanoscale (<100 nm), which are referred to as nanoplastics. Because of their high surface area, nanoplastic may bind hydrophobic chemicals very effectively, increasing their hazard when such nanoplastics are taken up by biota. The present study reports distribution coefficients for sorption of polycyclic aromatic hydrocarbons (PAHs) to 70 nm polystyrene in freshwater, and PAH adsorption isotherms spanning environmentally realistic aqueous concentrations of 10(-5)  μg/L to 1 μg/L. Nanopolystyrene aggregate state was assessed using dynamic light scattering. The adsorption isotherms were nonlinear, and the distribution coefficients at the lower ends of the isotherms were very high, with values up to 10(9) L/kg. The high and nonlinear sorption was explained from π-π interactions between the planar PAHs and the surface of the aromatic polymer polystyrene and was higher than for micrometer-sized polystyrene. Reduction of nanopolystyrene aggregate sizes had no significant effect on sorption, which suggests that the PAHs could reach the sorption sites on the pristine nanoparticles regardless of the aggregation state. Pre-extraction of the nanopolystyrene with C18 polydimethylsiloxane decreased sorption of PAHs, which could be explained by removal of the most hydrophobic fraction of the nanopolystyrene. Environ Toxicol Chem 2016;35:1650-1655. © 2015 SETAC.

  18. Critical analysis of the local aromaticity concept in polyaromatic hydrocarbons.

    Science.gov (United States)

    Bultinck, Patrick

    2007-01-01

    A large number of local aromaticity indices for the benzenoid rings in polyaromatic hydrocarbons is computed. The results are interpreted, supporting Clar's hypothesis, and mutual correlations are investigated. It is shown that there are good correlations between all indices that strictly allow comparing benzenoid character. Poor correlations are found with NICS. A rationale is offered, yielding the conclusion that NICS and ring current maps follow a fundamentally different path to local aromaticity. In this sense the lack of correlation is not due to a real multidimensional character of aromaticity but rather to confusion and vagueness of the aromaticity concept. PMID:17328438

  19. Fog processing of polycyclic aromatic hydrocarbons (PAH)

    Science.gov (United States)

    Wang, Y.; Khadapkar, K.; Ehrenhauser, F. S.; Hutchings, J. W.; Wornat, M. J.; Valsaraj, K. T.; Herckes, P.

    2010-07-01

    Polyaromatic hydrocarbons (PAHs) are a class of organic species of concern for environmental and human health. The present work will present initial finding of a comprehensive study on the fate of PAHs in multiphase fog/cloud systems and across consecutive fog/smog cycles. Field observations were conducted in Fresno, CA in Winter 2010. Simultaneous measurements of gas phase, aerosol and fog PAH allowed to gain insights on the partitioning of PAH in a multiphase fog system. Partitioning results as well as temporal evolution of PAH concentrations across different phases will be discussed. Select known degradation products (oxy-PAH) from the processing of PAHs were also analyzed in the fog systems, although frequently their concentrations were close to or below detection limits, even in the polluted urban study setting. The field observations are complemented by laboratory investigations on the reactivity of PAH in fog systems, both heterogeneously and in the aqueous phase. Heterogeneously a novel reactor design is being tested to simulate fog systems and allow for repeat fog/smog cycles. A separate series of measurements investigated the processing of PAH in the aqueous phase in a solar simulator set-up.

  20. Biodegradation of Various Aromatic Compounds by Enriched Bacterial Cultures: Part A-Monocyclic and Polycyclic Aromatic Hydrocarbons.

    Science.gov (United States)

    Oberoi, Akashdeep Singh; Philip, Ligy; Bhallamudi, S Murty

    2015-08-01

    Present study focused on the screening of bacterial consortium for biodegradation of monocyclic aromatic hydrocarbon (MAH) and polycyclic aromatic hydrocarbons (PAHs). Target compounds in the present study were naphthalene, acenaphthene, phenanthrene (PAHs), and benzene (MAH). Microbial consortia enriched with the above target compounds were used in screening experiments. Naphthalene-enriched consortium was found to be the most efficient consortium, based on its substrate degradation rate and its ability to degrade other aromatic pollutants with significantly high efficiency. Substrate degradation rate with naphthalene-enriched culture followed the order benzene > naphthalene > acenaphthene > phenanthrene. Chryseobacterium and Rhodobacter were discerned as the predominant species in naphthalene-enriched culture. They are closely associated to the type strain Chryseobacterium arthrosphaerae and Rhodobacter maris, respectively. Single substrate biodegradation studies with naphthalene (PAH) and benzene (MAH) were carried out using naphthalene-enriched microbial consortium (NAPH). Phenol and 2-hydroxybenzaldehyde were identified as the predominant intermediates during benzene and naphthalene degradation, respectively. Biodegradation of toluene, ethyl benzene, xylene, phenol, and indole by NAPH was also investigated. Monod inhibition model was able to simulate biodegradation kinetics for benzene, whereas multiple substrate biodegradation model was able to simulate biodegradation kinetics for naphthalene.

  1. Comments on Coulomb pairing in aromatic hydrocarbons

    CERN Document Server

    Huber, D L

    2013-01-01

    Recently reported anomalies in the double-photonionization spectra of aromatic molecules such as benzene, naphthalene, anthracene and coronene are attributed to Coulomb-pair resonances of pi electrons.

  2. Measurement of Aromatic-hydrocarbons With the DOAS Technique

    OpenAIRE

    Axelsson, H; Eilard, A.; Emanuelsson, A.; Galle, B.; Edner, Hans; Ragnarson, P; Kloo, H

    1995-01-01

    Long-path DOAS (differential optical absorption spectroscopy) in the ultraviolet spectral region has been shown to be applicable for low-concentration measurements of light aromatic hydrocarbons. However, because of spectral interferences among different aromatics as well as with oxygen, ozone, and sulfur dioxide, the application of the DOAS technique for this group of components is not without problems. This project includes a study of the differential absorption characteristics, between 250...

  3. High-resolution gas chromatographic analysis of polycyclic aromatic hydrocarbons and aliphatic hydrocarbons

    International Nuclear Information System (INIS)

    A study of the analysis by gas chromatography of aromatic polycyclic hydrocarbons and aliphatic hydrocarbons is presented. The separation has been carried out by glass and fused silica capillary column in two different polar stationary phases OV-1 and SE-54. The limitation and the advantages of the procedure are discussed in terms of separation, sensitivity and precision. (Author) 20 refs

  4. Fenton's reagent as a remediation process in water treatment: application to the degradation of polycyclic aromatic hydrocarbons in waters and sewage sludges; La reaction de fenton comme procede de rehabilitation dans le traitement des eaux: application a la degradation des hydrocarbures aromatiques polycycliques dans les eaux et les boues residuaires

    Energy Technology Data Exchange (ETDEWEB)

    Flotron, V.

    2004-05-15

    This study is related to the application of Fenton's reagent to remedy matrices contaminated by polycyclic aromatic hydrocarbons (PAHs). In aqueous solution, the choice of the reagent implementation is important, in order to generate enough radicals to oxidize pollutants. Degradation of the organic compounds is possible, but a large difference in reactivity is observed between 'alternant' and 'non-alternant' PAHs (with a five carbon atoms cycle). Besides, if a few specific precautions are omitted, the PAHs can sorb onto the flask inside surface, and therefore not undergo oxidation. The results on sewage sludges show that under certain conditions (high reagent concentrations), the pollutants can be oxidised although they are adsorbed. Moreover, it appears that the matrix itself plays an important role, as the iron oxides seem to be able to decompose hydrogen peroxide, and thus initiate Fenton reaction. Its application to contaminated soils and sediments is also possible. (author)

  5. Polycyclic’ Aromatic Hydrocarbon Induced Intracellular Signaling and Lymphocyte Apoptosis

    DEFF Research Database (Denmark)

    Schneider, Alexander M.

    The aryl hydrocarbon (dioxin) receptor (AhR) is a transcription factor possessing high affinity to potent environmental pollutants, polycyclic aromatic hydrocarbons (PAH) and related halogenated hydrocarbons (e.g. dioxins). Numerous research attribute toxicity of these compounds to the receptor...... novel mechanistic explanations for the toxicity of the known compounds. Another unanswered question of the AhR biochemistry is,” Which factors do control the AhP expression and activity?” Using fibroblast model, the role of a cell cycle in maintaining the AhR level was evaluated. The results...

  6. Bioremediation of Mixtures of High Molecular Weight Polycyclic Aromatic Hydrocarbons

    Science.gov (United States)

    Xu, H.; Wu, J.; Shi, X.; Sun, Y.

    2014-12-01

    Although bioremediation has been considered as one of the most promising means to remove polycyclic aromatic hydrocarbons (PAHs) from polluted environments, the efficacy of PAHs bioremediation still remains challenged, especially for high molecular weight PAHs (HMW PAHs) and their mixtures. This study was focused on (a) isolation and characterization of pure strain and mixed microbial communities able to degrade HMW PAHs and (b) further evaluation of the ability of the isolated microbes to degrade HMW PAHs mixtures in the absence and presence of indigenous flora. Fluoranthene, benzo[b]fluoranthene and pyrene were selected as the representative HMW PAHs in this study. A pure bacterial strain, identified as Herbaspirillum chlorophenolicum FA1, was isolated from activated sludge. A mixed bacterial community designated as consortium-4 was isolated from petroleum contaminated soils, containing Pseudomonas sp. FbP1、Enterobacter sp. FbP2、Hydrogenophaga sp. FbP3 and Luteolibacter pohnpeiensis. FbP4. To our knowledge, this is the first study to demonstrate that bacterial strains of Herbaspirillum chlorophenolicum FA1 and Luteolibacter pohnpeiensis. FbP4 can also degrade fluoranthene, benzo[b]fluoranthene and pyrene. Experiment results showed that both strain FA1 and consortium-4 could degrade fluoranthene, benzo[b]fluoranthene and pyrene within a wide range of temperature, pH and initial PAHs concentration. Degradation of HMW PAHs mixtures (binary and ternary) demonstrated the interactive effects that can alter the rate and extent of biodegradation within a mixture. The presence of indigenous flora was found to either increase or decrease the degradation of HMW PAHs, suggesting possible synergistic or competition effects. Biodegradation kinetics of HMW PAHs for sole substrates, binary and ternary systems was evaluated, with the purpose to better characterize and compare the biodegradation process of individual HMW PAH and mixtures of HMW PAHs. Results of this study

  7. Bioavailability of Polycyclic Aromatic Hydrocarbons in Soils and Sediments

    NARCIS (Netherlands)

    Cuypers, M.P.

    2001-01-01

    Polycyclic aromatic hydrocarbons (PAHs) constitute a group of priority pollutants which are of increasing environmental concern because of their adverse effects on humans, animals, and plants. Soils and sediments generally serve as a sink for PAHs, which leads to the accumulation of PAHs at contamin

  8. Polycyclic aromatic hydrocarbons in air samples of meat smokehouses

    DEFF Research Database (Denmark)

    Hansen, Åse Marie; Olsen, I L; Poulsen, O M

    1992-01-01

    In a screening programme nine Danish meat smokehouses were randomly selected for measurements on concentration of airborne polycyclic aromatic hydrocarbons (PAH). A total of 23 stationary air samples were collected during the entire working period of the kiln either above the kiln doors or approx...

  9. THE RATES OF POLYCYCLIC AROMATIC HYDROCARBON EMISSIONS FROM INCENSE BURNING

    Science.gov (United States)

    The paper presents the results of experiments performed to determine the amounts of gas- and particle-phase polycyclic aromatic hydrocarbons (PAHS) in incense smoke. Ten brands of incense, 3 of stick, 2 of joss stick, and one each of cone, smudge bundle, rope, powder, and rock, w...

  10. Extraction Techniques for Polycyclic Aromatic Hydrocarbons in Soils

    OpenAIRE

    Lau, E. V.; Gan, S.; Ng, H.K.

    2010-01-01

    This paper aims to provide a review of the analytical extraction techniques for polycyclic aromatic hydrocarbons (PAHs) in soils. The extraction technologies described here include Soxhlet extraction, ultrasonic and mechanical agitation, accelerated solvent extraction, supercritical and subcritical fluid extraction, microwave-assisted extraction, solid phase extraction and microextraction, thermal desorption and flash pyrolysis, as well as fluidised-bed extraction. The influencing factors in ...

  11. Interactions of polyhalogeneted aromatic hydrocarbons with thyroid hormone metabolism.

    NARCIS (Netherlands)

    Schuur, A.G.

    1998-01-01

    This thesis deals with the possible interactions of polyhalogenated aromatic hydrocarbons and/or their metabolites with thyroid hormone metabolism. This chapter summarizes firstly the effects of thyroid hormone on the induction of biotransformation enzymes by PHAHs. Secondly, the results on the inhi

  12. Polycyclic aromatic hydrocarbons (PAH) in Danish barbecued meat

    DEFF Research Database (Denmark)

    Duedahl-Olesen, Lene; Aaslyng, Margit Dall; Meinert, Lene;

    2015-01-01

    Barbecuing is known to result in the formation of polycyclic aromatic hydrocarbons (PAHs). A validated method that employed pressurized liquid extraction (PLE), gel permeation chromatography (GPC) followed by solid phase extraction (SPE) on Silica and analytical determination by GC-MS was applied...

  13. Biotransformation of polycyclic aromatic hydrocarbons in marine polychaetes

    DEFF Research Database (Denmark)

    Jørgensen, Anne; Giessing, Anders; Rasmussen, Lene Juel;

    2008-01-01

    Deposit-feeding polychaetes constitute the dominant macrofauna in marine environments that tend to be depositional centers for organic matter and contaminants. Polychaetes are known to accumulate polycyclic aromatic hydrocarbons (PAHs) from both particulate and dissolved phases but less is known...

  14. Polycyclic aromatic hydrocarbons in soils around Guanting Reservoir, Beijing, China

    NARCIS (Netherlands)

    Jiao, W.T.; Lu, Y.L.; Wang, T.Y.; Li, J.; Han, Jingyi; Wang, G.; Hu, W.Y.

    2009-01-01

    The concentrations of 16 polycyclic aromatic hydrocarbons ( 16PAHs) were measured by gas chromatography equipped with a mass spectrometry detector (GC-MS) in 56 topsoil samples around Guanting Reservior (GTR), which is an important water source for Beijing. Low to medium levels of PAH contamination

  15. Solubilization and biodegradation of polycyclic aromatic hydrocarbons in microemulsions

    Energy Technology Data Exchange (ETDEWEB)

    Wong, J.W.C.; Zhao, Z.Y.; Yang, J.; Wong, S.Y. [Hong Kong Baptist Univ., Hong Kong (China). Sino-Forest Applied Research Centre for Pearl River Delta Environment, Dept. of Biology

    2009-07-01

    This study investigated the feasibility of using microemulsions to enhance the biodegradation of polycyclic aromatic hydrocarbons (PAHs). Microemulsions are commonly used in soil washing as a means of enhancing the solubility of hydrophobic pollutants. The microemulsions were composed of Tween-80, 1-pentanol and linseed oil. Phenanthrene (PHE) was dissolved in dichloromethane and added to a glass vial. Microemulsions were added separately to the vials. A high performance liquid chromatograph (HPLC) was used to determine PHE concentrations. The vials were inoculated with an isolated PAH degradative bacterium Bacillus subtilis B-UM. Soil collected from abandoned shipyards in Hong Kong were then spiked with the mixtures and aged for 3 months. One way analysis of variance (ANOVA) analyses were conducted. Results of the study showed that a microemulsion composed of 0.4 Tween-80, 0.1 per cent 1-pentanol, and 0.05 linseed oil effectively enhanced the biodegradation of PHE in the aqueous phase. It was concluded that microemulsions can be used to remediate soils contaminated by PAHs. 26 refs., 2 tabs., 4 figs.

  16. Kinetic double-layer model of aerosol surface chemistry and gas-particle interactions (K2-SURF: degradation of polycyclic aromatic hydrocarbons exposed to O3, NO2, H2O, OH and NO3

    Directory of Open Access Journals (Sweden)

    U. Pöschl

    2009-09-01

    Full Text Available We present a kinetic double-layer surface model (K2-SURF that describes the degradation of polycyclic aromatic hydrocarbons (PAHs on aerosol particles exposed to ozone, nitrogen dioxide, water vapor, hydroxyl and nitrate radicals. The model is based on multiple experimental studies of PAH degradation and on the PRA framework (Pöschl et al., 2007 for aerosol and cloud surface chemistry and gas-particle interactions. For a wide range of substrates, including solid and liquid organic and inorganic substances (soot, silica, sodium chloride, octanol/decanol, organic acids, etc., the concentration- and time-dependence of the heterogeneous reaction between PAHs and O3 can be efficiently described with a Langmuir-Hinshelwood-type mechanism. Depending on the substrate material, the Langmuir adsorption constants for O3 vary over three orders of magnitude (Kads,O3≈10−15–10−13 cm3, and the second-order rate coefficients for the surface layer reaction of O3 with different PAH vary over two orders of magnitude (kSLR,PAH,O3≈10−18–10−17 cm2 s−1. The available data indicate that the Langmuir adsorption constants for NO2 are similar to those of O3, while those of H2O are several orders of magnitude smaller (Kads,H2O≈10−18–10−17 cm3. The desorption lifetimes and adsorption enthalpies inferred from the Langmuir adsorption constants suggest chemisorption of NO2 and O3 – possibly in the form of O atoms – and physisorption of H2O. The K2-SURF model enables the calculation of ozone uptake coefficients, γO3, and of PAH concentrations in the quasi-static particle surface layer. Competitive adsorption and chemical transformation of the surface (aging lead to a strong non-linear dependence of γO3 on time and gas phase composition, with different characteristics under dilute atmospheric and concentrated laboratory conditions. Under typical ambient conditions, γO3 of PAH-coated aerosol particles are expected to be in the range of 10−6–10

  17. Distributions of polycyclic aromatic hydrocarbons and alkylated polycyclic aromatic hydrocarbons in Osaka Bay, Japan

    International Nuclear Information System (INIS)

    Highlights: • Contamination of sediment by PAHs and alkylated PAHs was investigated in Osaka Bay. • The major sources appeared to be pyrogenic or both pyrogenic and petrogenic. • PAH concentrations were remarkably high at a site near Kobe. • PAHs in Kobe may have been derived from the fire associated with the earthquake. - Abstract: Contaminations in sediments by polycyclic aromatic hydrocarbons (PAHs) and alkylated PAHs were investigated at 44 sites in Osaka Bay, Japan. Concentrations of total PAHs and alkylated PAHs were in the range 6.40–7800 ng/g dry weights and 13.7–1700 ng/g dry weights, respectively. The PAH concentrations tended to be higher along the shoreline in the vicinities of big ports, industrialized areas, and densely populated regions such as the cities of Osaka and Kobe. The major sources appeared to be pyrogenic or both pyrogenic and petrogenic at most of the sites. PAH concentrations were remarkably high at a site near Kobe, where the concentrations of dibenzo(a,h)anthracene and benzo(g,h,i)perylene exceeded the effects-range-medium concentration and eight PAHs were above the corresponding effects-range-low concentrations. Those PAHs may have been derived from the great fire associated with the large earthquake in 1995

  18. Growth of fungi on volatile aromatic hydrocarbons

    NARCIS (Netherlands)

    Prenafeta Boldú, F.X.

    2002-01-01

    The present study aimed the better understanding of the catabolism of monoaromatic hydrocarbons by fungi. This knowledge can be used to enhance the biodegradation of BTEX pollutants. Fungi with the capacity of using toluene as the sole source of carbon and energy were isolated by enriching environme

  19. Correlation between atmospheric polycyclic aromatic hydrocarbons exposure and urinary hydroxyl metabolites of polycyclic aromatic hydrocarbons in elderly population in Tianjin

    Institute of Scientific and Technical Information of China (English)

    秦晓蕾

    2013-01-01

    Objective To identify suitable hydroxyl polycyclic aromatic hydrocarbons(OH-PAHs) for co-evaluation of internal exposure level of PAHs by simultaneous determination of a variety of OH-PAHs in urine. Methods The 24-h individual particulate matter and morning urine

  20. 盐碱土壤多环芳烃降解菌群筛选及其降解特性%Screening and Biodegradation Characteristics of Polycyclic Aromatic Hydrocarbons-Degrading Consortium From Saline-Alkali Soil

    Institute of Scientific and Technical Information of China (English)

    宋立超; 刘灵芝; 李培军; 刘宛; 张玉龙

    2012-01-01

    为了强化多环芳烃(PAHs)污染盐碱土壤原位微生物修复的应用,并提供高效的菌种资源,从天津大港油田盐碱化的油污土壤中富集分离出1组高效降解菲、芘的耐盐碱菌群,分离获得可培养优势细菌5株、真菌3株,考察了该菌群对菲、芘的降解效果,并进行了其对菲、芘降解特性分析.结果表明,该菌群在菲、芘质量浓度分别为25、50和75 mg/L的液体无机盐培养基中培养15 d,菲、芘的降解率分别达到75.3%和53.6%、56.6%和52.0%、25.2%和13.6%;该菌群对菲、芘降解具有较广泛的盐质量分数和pH值范围,在菲、芘初始质量浓度各为50 mg/L,最适盐质量分数0~2%,最适pH值8.6条件下,添加质量分数0.4%葡萄糖培养15d后,菲、芘的降解率显著提高,达到92.1%和65.8%.细菌16S rDNA和真菌18S rDNA测序结果表明,该菌群由叶杆菌属(Phyllobacterium)、假单胞菌属(Pseudomonas)、盐单胞属(Halomonas)、泛菌属(Pantoea)和青霉属(Penicillium)、双曲孢属(Sigmoidea)、胶孢炭疽属(Colletotrichum)组成.%The salt and alkaline endurable microbial consortium of degrading phenanthrene and pyrene effectively was developed from oil-contaminated saline-alkali soil of Tianjin Dagang oil field to intensify the application of situ bioremediation of polycyclic aromatic hydrocarbons in saline-alkaline soil and to provide highly effective microorganisms resources. Five cultivable dominate bacterium strains and three fungi strains through separation were obtained, and their degradation characteristics for phenanthrene and pyrene were analyzed. The degradation rates of phenanthrene and pyrene with 25, 50 and 75 mg/L initial concentration by the microbial consortium in liquid mineral medium after 15 d cultivation were 75. 3% and 53. 6%, 56. 6% and 52. 0%, 25. 2% and 13.6% respectively, meanwhile, when the initial concentration of phenanthrene and pyrene was 50 mg/L, respectively, the most

  1. Bioavailability and biodegradation of polycyclic aromatic hydrocarbons.

    NARCIS (Netherlands)

    Volkering, F.

    1996-01-01

    One of the main problems in biological soil remediation is the slow or incomplete degradation of hydrophobic organic pollutants. The principal reason for this problem is the fact that these compounds bind strongly to the soil matrix or occur as a separate non- aqueous phase in the soil. As most micr

  2. Mechanistic studies on the OH-initiated atmospheric oxidation of selected aromatic hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Nehr, Sascha

    2012-07-01

    Benzene, toluene, the xylenes, and the trimethylbenzenes are among the most abundant aromatic trace constituents of the atmosphere mainly originating from anthropogenic sources. The OH-initiated atmospheric photo-oxidation of aromatic hydrocarbons is the predominant removal process resulting in the formation of O{sub 3} and secondary organic aerosol. Therefore, aromatics are important trace constituents regarding air pollution in urban environments. Our understanding of aromatic photo-oxidation processes is far from being complete. This work presents novel approaches for the investigation of OH-initiated atmospheric degradation mechanisms of aromatic hydrocarbons. Firstly, pulsed kinetic studies were performed to investigate the prompt HO{sub 2} formation from OH+ aromatic hydrocarbon reactions under ambient conditions. For these studies, the existing OH reactivity instrument, based on the flash photolysis/laser-induced fluorescence (FP/LIF) technique, was extended to the detection of HO{sub 2} radicals. The experimental design allows for the determination of HO{sub 2} formation yields and kinetics. Results of the pulsed kinetic experiments complement previous product studies and help to reduce uncertainties regarding the primary oxidation steps. Secondly, experiments with aromatic hydrocarbons were performed under atmospheric conditions in the outdoor atmosphere simulation chamber SAPHIR (Simulation of Atmospheric PHotochemistry In a large Reaction chamber) located at Forschungszentrum Juelich. The experiments were aimed at the evaluation of up-to-date aromatic degradation schemes of the Master Chemical Mechanism (MCMv3.2). The unique combination of analytical instruments operated at SAPHIR allows for a detailed investigation of HO{sub x} and NO{sub x} budgets and for the determination of primary phenolic oxidation product yields. MCMv3.2 deficiencies were identified and most likely originate from shortcomings in the mechanistic representation of ring

  3. Exposure of iron foundry workers to polycyclic aromatic hydrocarbons

    DEFF Research Database (Denmark)

    Omland, Øyvind; Sherson, D; Hansen, Åse Marie;

    1994-01-01

    Exposure to polycyclic aromatic hydrocarbons (PAHs) in foundry workers has been evaluated by determination of benzo(a)pyrene-serum albumin adducts and urinary 1-hydroxypyrene. Benzo(a)pyrene binding to albumin and 1-hydroxypyrene were quantitatively measured by enzyme linked immunosorbent assay...... (ELISA) and reverse phase high performance liquid chromatography (HPLC), respectively. 70 male foundry workers and 68 matched controls were investigated. High and low exposure groups were defined from breathing zone hygienic samples, consisting of 16 PAH compounds in particulate and gaseous phase. Mean...... than in smoking and non-smoking controls (0 (0-0.022) and 0 (0-0.010) mumol/mol creatinine). Dose-response relations between total PAH, pyrene, carcinogenic PAHs, and 1-hydroxypyrene for smokers, and polycyclic aromatic hydrocarbons adsorbed to dust for non-smokers are suggested. Exposure to PAHs...

  4. Radiolytic degradation of chlorinated hydrocarbons in water

    International Nuclear Information System (INIS)

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

  5. Polycyclic aromatic hydrocarbons in some grounded coffee brands.

    Science.gov (United States)

    Grover, Inderpreet Singh; Sharma, Rashmi; Singh, Satnam; Pal, Bonamali

    2013-08-01

    Potentially toxic 16 priority polycyclic aromatic hydrocarbons (PAHs) were determined in four brands of grounded coffee. Four to 13 PAHs were detected. Concentrations of total PAHs in different brands of coffee samples were in the range of 831.7-1,589.7 μg/kg. Benzo[a]pyrene (2A: probable human carcinogen) was found in Nescafe Premium whereas naphthalene (2B: possible human carcinogen) was found in all the samples of coffee. PMID:23242460

  6. THE INFRARED SPECTROSCOPY OF NEUTRAL POLYCYCLIC AROMATIC HYDROCARBON CLUSTERS

    Energy Technology Data Exchange (ETDEWEB)

    Ricca, Alessandra [Carl Sagan Center, SETI Institute, 189 Bernardo Avenue, Suite 100, Mountain View, CA 94043 (United States); Bauschlicher, Charles W. Jr. [Entry Systems and Technology Division, Mail Stop 230-3, NASA Ames Research Center, Moffett Field, CA 94035 (United States); Allamandola, Louis J., E-mail: Alessandra.Ricca-1@nasa.gov, E-mail: Charles.W.Bauschlicher@nasa.gov [Space Science Division, Mail Stop 245-6, NASA Ames Research Center, Moffett Field, CA 94035 (United States)

    2013-10-10

    The mid-infrared spectra of neutral homogeneous polycyclic aromatic hydrocarbon (PAH) clusters have been computed using density functional theory including an empirical correction for dispersion. The C-H out-of-plane bending modes are redshifted for all the clusters considered in this work. The magnitude of the redshift and the peak broadening are dependent on PAH size, shape, and on the PAH arrangement in the cluster.

  7. Polycyclic aromatic hydrocarbon (PAH) occurrence and remediation methods

    OpenAIRE

    Henner, Pascale; Schiavon, Michel; Morel, Jean-Louis; Lichtfouse, Eric

    1997-01-01

    International audience Polycyclic aromatic hydrocarbons (PAHs) are potentially mutagenic and carcinogenic substances occurring at various concentrations in atmosphere, soils, waters and sediments. PAHs, inherited both from natural and anthropogenic processes, are persistent organic pollutants (POP) due to their chemical stability and biodegradation resistance. The increase of road transportation, and of industrial and agricultural activities has led to a notable build up of PAH amounts in ...

  8. Interactions of polyhalogeneted aromatic hydrocarbons with thyroid hormone metabolism.

    OpenAIRE

    Schuur, A.G.

    1998-01-01

    This thesis deals with the possible interactions of polyhalogenated aromatic hydrocarbons and/or their metabolites with thyroid hormone metabolism. This chapter summarizes firstly the effects of thyroid hormone on the induction of biotransformation enzymes by PHAHs. Secondly, the results on the inhibition of thyroid hormone sulfation by hydroxylated metabolites of PHAH are summarized. Some conclusions and remarks on the overall implications of the results are given at the end of this chapter....

  9. Capacity of Aromatic Compound Degradation by Bacteria from Amazon Dark Earth

    Directory of Open Access Journals (Sweden)

    Fernanda Mancini Nakamura

    2014-06-01

    Full Text Available Amazon dark earth (ADE is known for its high organic matter content, biochar concentration and microbial diversity. The biochar amount suggests the existence of microorganisms capable of degrading aromatic hydrocarbons (AHs. In an effort to investigate the influence of bacteria on the resilience and fertility of these soils, we enriched five ADE soils with naphthalene and phenanthrene, and biodegradation assays with phenanthrene and diesel oil were carried out, as well. After DNA extraction, amplification and sequencing of the 16S rRNA bacterial gene, we identified 148 isolates as the Proteobacteria, Firmicutes and Actinobacteria phyla comprising genera closely related to AHs biodegradation. We obtained 128 isolates that degrade diesel oil and 115 isolates that degrade phenanthrene. Some isolates were successful in degrading both substrates within 2 h. In conclusion, the obtained isolates from ADE have degrading aromatic compound activity, and perhaps, the biochar content has a high influence on this.

  10. Les hydrocarbures aromatiques polycycliques dans l'environnement. Deuxième partie : La dégradation par voie microbienne Polycyclic Aromatic Hydrocarbons in the Environment. Part Two: Microbial Degradation

    Directory of Open Access Journals (Sweden)

    Bouchez M.

    2006-11-01

    Full Text Available La microbiologie de la dégradation des hydrocarbures aromatiques polycycliques (HAP est un domaine de recherche en plein développement. C'est à la fois le devenir dans l'environnement de ces composés ubiquistes et génotoxiques et l'utilisation de procédés microbiologiques de dépollution des sols industriels contaminés par ces produits qui motivent cet intérêt. On présente ici une synthèse des connaissances actuelles dans ce domaine. Les organismes dégradeurs sont essentiellement les bactéries et les champignons. Le processus de dégradation, aérobie, est initié par des oxygénases. Les bactéries utilisent les HAP de deux à quatre cycles comme substrats de croissance, ce qui conduit à leur minéralisation. Les champignons, lignolytiques et non lignolytiques, attaquent les HAP par cométabolisme, ce que font également les bactéries. L'ensemble des micro-organismes dégradant les HAP, et les voies métaboliques impliquées, sont présentés. Le mode d'accession des micro-organismes à leurs substrats très peu solubles est un point important. Les études menées avec les bactéries ont montré l'existence de deux mécanismes, le transfert par solubilisation dans la phase aqueuse et l'accession interfaciale directe. Un autre aspect présenté est le devenir des HAP, en termes de bilans carbone, lors de la dégradation bactérienne de HAP individuels et de mélanges de HAP. Des taux de minéralisation élevés peuvent être obtenus. Dans le cas des mélanges, ces taux élevés impliquent la mise en oeuvre de microflores complexes où le cométabolisme joue un rôle important. Les progrès accomplis ces dernières années conduisent à ne plus considérer les HAP comme des composés intrinsèquement récalcitrants à la biodégradation. Dans l'environnement, un facteur important limitant la dégradation des HAP est leur accessibilité aux micro-organismes. The microbiology of the degradation of polycyclic aromatic hydrocarbons

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

    Science.gov (United States)

    Marco-Urrea, Ernest; García-Romera, Inmaculada; Aranda, Elisabet

    2015-12-25

    In previous decades, white-rot fungi as bioremediation agents have been the subjects of scientific research due to the potential use of their unspecific oxidative enzymes. However, some non-white-rot fungi, mainly belonging to the Ascomycota and Zygomycota phylum, have demonstrated their potential in the enzymatic transformation of environmental pollutants, thus overcoming some of the limitations observed in white-rot fungi with respect to growth in neutral pH, resistance to adverse conditions and the capacity to surpass autochthonous microorganisms. Despite their presence in so many soil and water environments, little information exists on the enzymatic mechanisms and degradation pathways involved in the transformation of hydrocarbons by these fungi. This review describes the bioremediation potential of non-ligninolytic fungi with respect to chlorinated hydrocarbons and polycyclic aromatic hydrocarbons (PAHs) and also shows known conversion pathways and the prospects for future research.

  12. Isolation and Characterization of Hydrocarbon-Degrading Yeast Strains from Petroleum Contaminated Industrial Wastewater

    Directory of Open Access Journals (Sweden)

    Boutheina Gargouri

    2015-01-01

    Full Text Available Two yeast strains are enriched and isolated from industrial refinery wastewater. These strains were observed for their ability to utilize several classes of petroleum hydrocarbons substrates, such as n-alkanes and aromatic hydrocarbons as a sole carbon source. Phylogenetic analysis based on the D1/D2 variable domain and the ITS-region sequences indicated that strains HC1 and HC4 were members of the genera Candida and Trichosporon, respectively. The mechanism of hydrocarbon uptaking by yeast, Candida, and Trichosporon has been studied by means of the kinetic analysis of hydrocarbons-degrading yeasts growth and substrate assimilation. Biodegradation capacity and biomass quantity were daily measured during twelve days by gravimetric analysis and gas chromatography coupled with mass spectrometry techniques. Removal of n-alkanes indicated a strong ability of hydrocarbon biodegradation by the isolated yeast strains. These two strains grew on long-chain n-alkane, diesel oil, and crude oil but failed to grow on short-chain n-alkane and aromatic hydrocarbons. Growth measurement attributes of the isolates, using n-hexadecane, diesel oil, and crude oil as substrates, showed that strain HC1 had better degradation for hydrocarbon substrates than strain HC4. In conclusion, these yeast strains can be useful for the bioremediation process and decreasing petroleum pollution in wastewater contaminated with petroleum hydrocarbons.

  13. Assessment of the bioavailability and phytotoxicity of sediment spiked with polycyclic aromatic hydrocarbons.

    Science.gov (United States)

    Rončević, Srđan; Spasojević, Jelena; Maletić, Snežana; Jazić, Jelena Molnar; Isakovski, Marijana Kragulj; Agbaba, Jasmina; Grgić, Marko; Dalmacija, Božo

    2016-02-01

    Large amounts of sediment are dredged globally every year. This sediment is often contaminated with low concentrations of metals, polycyclic aromatic hydrocarbons, pesticides and other organic pollutants. Some of this sediment is disposed of on land, creating a need for risk assessment of the sediment disposal method, to minimize the degradation of environmental quality and prevent risks to human health. Evaluating the available fractions of certain polycyclic aromatic hydrocarbons is very important, as in the presence of various organisms, they are believed to be easily subject to the processes of bioaccumulation, biosorption and transformation. In order to determine the applicability of applying these methods for the evaluation of pollutant bioavailability in sediments, the desorption kinetics from the sediment of various polycyclic aromatic hydrocarbons in the presence of Tenax and XAD4 were examined over the course of 216 h. Changes in the PAH concentrations in dredged sediments using five different seed plants during a short time of period (10 days) were also followed. Using chemical extraction techniques with Tenax and XAD4, a time of around 24 h is enough to achieve equilibrium for all four PAHs. Results showed good agreement between the seed accumulation and PAH extraction methods with both agents. If we compare the two extraction techniques, XAD4 gave better results for phenanthrene, pyrene and benzo(a)pyrene, and Tenax gave better results for chrysene. PMID:26490893

  14. Comparative Genomics of the Ubiquitous, Hydrocarbon-degrading Genus Marinobacter

    Science.gov (United States)

    Singer, E.; Webb, E.; Edwards, K. J.

    2012-12-01

    The genus Marinobacter is amongst the most ubiquitous in the global oceans and strains have been isolated from a wide variety of marine environments, including offshore oil-well heads, coastal thermal springs, Antarctic sea water, saline soils and associations with diatoms and dinoflagellates. Many strains have been recognized to be important hydrocarbon degraders in various marine habitats presenting sometimes extreme pH or salinity conditions. Analysis of the genome of M. aquaeolei revealed enormous adaptation versatility with an assortment of strategies for carbon and energy acquisition, sensation, and defense. In an effort to elucidate the ecological and biogeochemical significance of the Marinobacters, seven Marinobacter strains from diverse environments were included in a comparative genomics study. Genomes were screened for metabolic and adaptation potential to elucidate the strategies responsible for the omnipresence of the Marinobacter genus and their remedial action potential in hydrocarbon-polluted waters. The core genome predominantly encodes for key genes involved in hydrocarbon degradation, biofilm-relevant processes, including utilization of external DNA, halotolerance, as well as defense mechanisms against heavy metals, antibiotics, and toxins. All Marinobacter strains were observed to degrade a wide spectrum of hydrocarbon species, including aliphatic, polycyclic aromatic as well as acyclic isoprenoid compounds. Various genes predicted to facilitate hydrocarbon degradation, e.g. alkane 1-monooxygenase, appear to have originated from lateral gene transfer as they are located on gene clusters of 10-20% lower GC-content compared to genome averages and are flanked by transposases. Top ortholog hits are found in other hydrocarbon degrading organisms, e.g. Alcanivorax borkumensis. Strategies for hydrocarbon uptake encoded by various Marinobacter strains include cell surface hydrophobicity adaptation via capsular polysaccharide biosynthesis and attachment

  15. Novel Approach for Evaluating Secondary Organic Aerosol from Aromatic Hydrocarbons: SOA Yield and Chemical Composition

    Science.gov (United States)

    Li, Lijie; Tang, Ping; Nakao, Shunsuke; Qi, Li; Kacarab, Mary; Cocker, David

    2016-04-01

    Aromatic hydrocarbons account for 20%-30% of urban atmospheric VOCs and are major contributors to anthropogenic secondary organic aerosol (SOA). However, prediction of SOA from aromatic hydrocarbons as a function of structure, NOx concentration, and OH radical levels remains elusive. Innovative SOA yield and chemical composition evaluation approaches are developed here to investigate SOA formation from aromatic hydrocarbons. SOA yield is redefined in this work by adjusting the molecular weight of all aromatic precursors to the molecular weight of benzene (Yield'= Yieldi×(MWi/MWBenzene); i: aromatic hydrocarbon precursor). Further, SOA elemental ratio is calculated on an aromatic ring basis rather than the classic mole basis. Unified and unique characteristics in SOA formed from aromatic hydrocarbons with different alkyl groups (varying in carbon number and location on aromatic ring) are explored by revisiting fifteen years of UC Riverside/CE-CERT environmental chamber data on 129 experiments from 17 aromatic precursors at urban region relevant low NOx conditions (HC:NO 11.1-171 ppbC:ppb). Traditionally, SOA mass yield of benzene is much greater than that of other aromatic species. However, when adjusting for molecular weight, a similar yield is found across the 17 different aromatic precursors. More importantly, four oxygens per aromatic ring are observed in the resulting SOA regardless of the alkyl substitutes attached to the ring, which majorly affect H/C ratio in SOA. Therefore, resulting SOA bulk composition from aromatic hydrocarbons can be predicted as C6+nH6+2nO4 (n: alkyl substitute carbon number). Further, the dominating role of the aromatic ring carbons is confirmed by studying the chemical composition of SOA formed from the photooxidation of an aromatic hydrocarbon with a 13C isotopically labeled alkyl carbon. Overall, this study unveils the similarity in SOA formation from aromatic hydrocarbons enhancing the understanding of SOA formation from

  16. The formation of polycyclic aromatic hydrocarbons in evolved circumstellar environments

    CERN Document Server

    Cherchneff, Isabelle

    2010-01-01

    The formation of Polycyclic Aromatic Hydrocarbons in the circumstellar outflows of evolved stars is reviewed, with an emphasis on carbon stars on the Asymptotic Giant Branch. Evidence for PAHs present in their winds is provided by meteoritic studies and recent observations of the Unidentified Infrared bands. We detail the chemical processes leading to the closure of the first aromatic ring as well as the growth mechanisms leading to amorphous carbon grains. Existing studies on PAH formation in evolved stellar envelopes are reviewed and new results for the modelling of the inner wind of the archetype carbon star IRC+10216 are presented. Benzene, C6H6, forms close to the star, as well as water, H2O, as a result of non-equilibrium chemistry induced by the periodic passage of shocks. The growth process of aromatic rings may thus resemble that active in sooting flames due to the presence of radicals like hydroxyl, OH. Finally, we discuss possible formation processes for PAHs and aromatic compounds in the hydrogen-...

  17. Exposure to polycyclic aromatic hydrocarbons with special focus on cancer

    Directory of Open Access Journals (Sweden)

    Thamaraiselvan Rengarajan

    2015-03-01

    Full Text Available Polycyclic aromatic hydrocarbons (PAHs are a group of compounds consisting of two or more fused aromatic rings. Most of them are formed during incomplete combustion of organic materials such as wood and fossil fuels, petroleum products, and coal. The composition of PAH mixtures varies with the source and is also affected by selective weathering effects in the environment. PAHs are ubiquitous pollutants frequently found in a variety of environments such as fresh water and marine sediments, the atmosphere, and ice. Due to their widespread distribution, the environmental pollution due to PAHs has aroused global concern. Many PAHs and their epoxides are highly toxic, mutagenic and/or carcinogenic to microorganisms as well as to higher forms of life including humans. The main aim of this review is to provide contemporary information on PAH sources, route of exposure, worldwide emission rate, and adverse effects on humans, especially with reference to cancer.

  18. Extraction Techniques for Polycyclic Aromatic Hydrocarbons in Soils

    Directory of Open Access Journals (Sweden)

    E. V. Lau

    2010-01-01

    Full Text Available This paper aims to provide a review of the analytical extraction techniques for polycyclic aromatic hydrocarbons (PAHs in soils. The extraction technologies described here include Soxhlet extraction, ultrasonic and mechanical agitation, accelerated solvent extraction, supercritical and subcritical fluid extraction, microwave-assisted extraction, solid phase extraction and microextraction, thermal desorption and flash pyrolysis, as well as fluidised-bed extraction. The influencing factors in the extraction of PAHs from soil such as temperature, type of solvent, soil moisture, and other soil characteristics are also discussed. The paper concludes with a review of the models used to describe the kinetics of PAH desorption from soils during solvent extraction.

  19. Polycylcic Aromatic Hydrocarbons (PAH's) in dense cloud chemistry

    OpenAIRE

    Wakelam, Valentine; Herbst, Eric

    2008-01-01

    Accepted to ApJ Virtually all detailed gas-phase models of the chemistry of dense interstellar clouds exclude polycyclic aromatic hydrocarbons (PAH's). This omission is unfortunate because from the few studies that have been done on the subject, it is known that the inclusion of PAH's can affect the gas-phase chemistry strongly. We have added PAH's to our network to determine the role they play in the chemistry of cold dense cores. In the models presented here, we include radiative attachm...

  20. Failure of hydrogenation in protecting polycyclic aromatic hydrocarbons from fragmentation

    CERN Document Server

    Gatchell, Michael; de Ruette, Nathalie; Chen, Tao; Giacomozzi, Linda; Nascimento, Rodrigo F; Wolf, Michael; Anderson, Emma K; Delaunay, Rudy; Viziano, Violaine; Rousseau, Patrick; Adoui, Lamri; Huber, Bernd A; Schmidt, Henning T; Zettergren, Henning; Cederquist, Henrik

    2015-01-01

    A recent study of soft X-ray absorption in native and hydrogenated coronene cations, C$_{24}$H$_{12+m}^+$ $m=0-7$, led to the conclusion that additional hydrogen atoms protect (interstellar) Polycyclic Aromatic Hydrocarbon (PAH) molecules from fragmentation [Reitsma et al., Phys. Rev. Lett. 113, 053002 (2014)]. The present experiment with collisions between fast (30-200 eV) He atoms and pyrene (C$_{16}$H$_{10+m}^+$, $m=0$, 6, and 16) and simulations without reference to the excitation method suggests the opposite. We find that the absolute carbon-backbone fragmentation cross section does not decrease but increases with the degree of hydrogenation for pyrene molecules.

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

    Science.gov (United States)

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

    2009-02-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

    Fu, S.; Li, K.; Xia, X.J.; Xu, X.B. [Chinese Academy of Sciences, Beijing (China)

    2009-02-15

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

  3. Polycyclic aromatic hydrocarbons - Primitive pigment systems in the prebiotic environment

    Science.gov (United States)

    Deamer, D. W.

    1992-01-01

    The chemical evolution of meteoritic organics in the primitive earth is examined experimentally with attention given to the photochemical effects of hydrocarbon/water mixtures. Also addressed are the generation of amphiphilic products by photochemical reactions and the transduction of light energy into potentially useful forms. Polycyclic aromatic hydrocarbons (PAHs) absorb light and exist in carbonaceous chondrites; PAHs are therefore examined as primitive pigments by means of salt solutions with pyrene, fluoranthene, and pyrene derivatives with hexadecane. The hexadecane undergoes photochemical oxidation and yields long-chain amphiphiles with oxygen supplied by water, and acid pH shifts also occur. PAHs are also tested in lipid bilayer membranes to examine light-energy transduction. Protons are found to accumulate within the membrane-bounded volume to form proton gradients, and this reaction is theorized to be a good model of primitive photochemical reactions that related to the transduction of light energy into useable forms.

  4. Environmental Behavior, Sources, and Effects of Chlorinated Polycyclic Aromatic Hydrocarbons

    Directory of Open Access Journals (Sweden)

    Takeshi Ohura

    2007-01-01

    Full Text Available The environmental sources and behaviors of chlorinated 2- to 5-ring polycyclic aromatic hydrocarbons (ClPAHs. ClPAHs are ubiquitous contaminants found in urban air, vehicle exhaust gas, snow, tap water, and sediments. The concentrations of ClPAHs in each of these environments are generally higher than those of dioxins but markedly lower than the concentrations of the parent compounds, PAHs. Environmental data and emission sources analysis for ClPAHs reveal that the dominant process of generation is by reaction of PAHs with chlorine in pyrosynthesis. This secondary reaction process also occurs in aquatic environments. Certain ClPAHs show greater toxicity, such as mutagenicity and aryl hydrocarbon receptor activity, than their corresponding parent PAHs. Investigation of the sources and environmental behavior of ClPAHs is of great importance in the assessment of human health risks.

  5. Biodegradation Of Polycyclic Aromatic Hydrocarbons In Petroleum Oil Contaminating The Environment

    International Nuclear Information System (INIS)

    Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous pollutants in urban atmospheres (Chen et al., 2013). PAHs enter the environment via incomplete combustion of fossil fuels and accidental leakage of petroleum products, and as components of products such as creosote (Muckian et al., 2009). Due to PAHs carcinogenic activity, they have been included in the European Union (EU) and the Environmental Protection Agency (EPA) priority pollutant lists. Human exposure to PAHs occurs in three ways, inhalation, dermal contact and consumption of contaminated foods, which account for 88-98% of such contamination; in other words, diet is the major source of human exposure to these contaminants (Rey-Salgueiro et al., 2008). Both the World Health Organization and the UK Expert Panel on Air Quality Standards (EPAQS) have considered benzo(a)pyrene (BaP) as a marker of the carcinogenic potency of the polycyclic aromatic hydrocarbons (PAH) mixture (Delgado-Saborit et al., 2011). Polycyclic aromatic and heavier aliphatic hydrocarbons, which have a stable recalcitrant molecular structure, exhibit high hydrophobicity and low aqueous solubility, are not readily removed from soil through leaching and volatilization (Brassington et al., 2007). The hydrophobicity of PAHs limits desorption to the aqueous phase (Donlon et al., 2002). Six main ways of dissipation, i.e. disappearance, are recognized in the environment: volatilization, photooxidation, Aim of the Work chemical oxidation, sorption, leaching and biodegradation. Microbial degradation is considered to be the main process involved in the dissipation of PAH (Yuan et al., 2002). Thus, more and more research interests are turning to the biodegradation of PAHs. Some microorganisms can utilize PAHs as a source of carbon and energy so that PAHs can be degraded to carbon dioxide and water, or transformed to other nontoxic or low-toxic substances (Perelo, 2010). Compared with other physical and chemical methods such as combustion

  6. Halotolerance and effect of salt on hydrophobicity in hydrocarbon-degrading bacteria.

    Science.gov (United States)

    Longang, Adégilns; Buck, Chris; Kirkwood, Kathlyn M

    2016-01-01

    Hydrocarbon-contaminated environments often also experience co-contamination with elevated levels of salt. This paper investigates the occurrence of halotolerance among several hydrocarbon-degrading bacteria, as an initial assessment of the importance of salt contamination to bioremediation strategies. Halotolerance was common, but not ubiquitous, among the 12 hydrocarbon-degrading bacteria tested, with many strains growing at up to 75 or 100 g NaCl L(-1) in rich medium. Greater sensitivity to elevated salt concentrations was observed among aromatics degraders compared to saturates degraders, and in defined medium compared to rich medium. Observed effects of high salt concentrations included increased lag times and decreased maximum growth. Many strains exhibited flocculation at elevated salt concentrations, but this did not correlate to any patterns in cell surface hydrophobicity, measured using the Bacterial Adhesion to Hydrocarbon assay. The occurrence of halotolerance in hydrocarbon-degrading bacteria suggests the potential for native microorganisms to contribute to the bioremediation of oil and salt co-contaminated sites, and indicates the need for a better understanding of the relationship between halotolerance and hydrocarbon biodegradation capabilities. PMID:26915518

  7. Polycyclic aromatic hydrocarbon composition in soils and sediments of high altitude lakes

    Energy Technology Data Exchange (ETDEWEB)

    Grimalt, Joan O.; Drooge, Barend L. van; Ribes, Alejandra; Fernandez, Pilar; Appleby, Peter

    2004-09-01

    Polycyclic aromatic hydrocarbons (PAH) in lake sediments and nearby soils of two European high mountain regions, Pyrenees and Tatra, have been studied. Similar mixtures of parent PAH were observed in all cases, indicating predominance of airborne transported combustion products. Nevertheless, the composition of these atmospherically long-range transported PAH was better preserved in the superficial layers of soils than sediments. This difference points to significant PAH degradation process, e.g. during lake water column transport, before accumulation in the latter. Post-depositional transformation was also different in both types of environmental compartments. Thus, lake sediments exhibit higher preservation of the more labile PAH involving lower degree of post-depositional oxidation. However, they also show the formation of major amounts of perylene by diagenetic transformation in the deep sections. This compound is not formed in soils where downcore enrichments of phenanthrene are observed, probably as a consequence of diagenetic aromatization of diterpenoids.

  8. Thermal neutron cross-section libraries for aromatic hydrocarbons

    Science.gov (United States)

    Cantargi, F.; Granada, J. R.

    2010-08-01

    Solid phases of aromatic hydrocarbons, such as benzene, toluene, mesitylene and a 3:2 mixture by volume of mesitylene and toluene, were studied as potential moderator materials for a cold neutron source. Existing information on the (lattice) translational and rotational modes of the different molecular species was used to produce generalized frequency spectra; the latter included the internal vibrational modes which in turn involved the analysis of the weights of the different modes. Cross-section libraries were generated in ENDF and ACE formats for hydrogen bounded in those materials at several temperatures, and were used in Monte Carlo calculations to analyze their neutron production compared with standard cryogenic materials like liquid hydrogen and solid methane, the best moderators in terms of cold neutron production. In particular, cross-section libraries were generated at 20 K, which is a typical operating temperature for the majority of the existing cold neutron sources. It was found that those aromatic hydrocarbons produce neutron spectra which are slightly warmer than that of solid methane while presenting a high resistance to radiation, conforming in this way a new and advantageous alternative to traditional moderator materials.

  9. Epoxy Coenzyme A Thioester pathways for degradation of aromatic compounds.

    Science.gov (United States)

    Ismail, Wael; Gescher, Johannes

    2012-08-01

    Aromatic compounds (biogenic and anthropogenic) are abundant in the biosphere. Some of them are well-known environmental pollutants. Although the aromatic nucleus is relatively recalcitrant, microorganisms have developed various catabolic routes that enable complete biodegradation of aromatic compounds. The adopted degradation pathways depend on the availability of oxygen. Under oxic conditions, microorganisms utilize oxygen as a cosubstrate to activate and cleave the aromatic ring. In contrast, under anoxic conditions, the aromatic compounds are transformed to coenzyme A (CoA) thioesters followed by energy-consuming reduction of the ring. Eventually, the dearomatized ring is opened via a hydrolytic mechanism. Recently, novel catabolic pathways for the aerobic degradation of aromatic compounds were elucidated that differ significantly from the established catabolic routes. The new pathways were investigated in detail for the aerobic bacterial degradation of benzoate and phenylacetate. In both cases, the pathway is initiated by transforming the substrate to a CoA thioester and all the intermediates are bound by CoA. The subsequent reactions involve epoxidation of the aromatic ring followed by hydrolytic ring cleavage. Here we discuss the novel pathways, with a particular focus on their unique features and occurrence as well as ecological significance.

  10. Recent studies in microbial degradation of petroleum hydrocarbons in hypersaline environments

    Directory of Open Access Journals (Sweden)

    Babu Zhereppa Fathepure

    2014-04-01

    Full Text Available Many hypersaline environments are often contaminated with petroleum compounds. Among these, oil and natural gas production sites all over the world and hundreds of kilometers of coastlines in the more arid regions of Gulf countries are of major concern due to the extent and magnitude of contamination. Because conventional microbiological processes do not function well at elevated salinities, bioremediation of hypersaline environments can only be accomplished using high salt-tolerant microorganisms capable of degrading petroleum compounds. In the last two decades, there have been many reports on the biodegradation of hydrocarbons in moderate to high salinity environments. Numerous microorganisms belonging to the domain Bacteria and Archaea have been isolated and their phylogeny and metabolic capacity to degrade a variety of aliphatic and aromatic hydrocarbons in varying salinities have been demonstrated. This article focuses on our growing understanding of bacteria and archaea responsible for the degradation of hydrocarbons under aerobic conditions in moderate to high salinity conditions. Even though organisms belonging to various genera have been shown to degrade hydrocarbons, members of the genera Halomonas Alcanivorax, Marinobacter, Haloferax, Haloarcula, and Halobacterium dominate the published literature. Despite rapid advances in understanding microbial taxa that degrade hydrocarbons under aerobic conditions, not much is known about organisms that carry out similar processes in anaerobic conditions. Also, information on molecular mechanisms and pathways of hydrocarbon degradation in high salinity is scarce and only recently there have been a few reports describing genes, enzymes and breakdown steps for some hydrocarbons. These limited studies have clearly revealed that degradation of oxygenated and non-oxygenated hydrocarbons by halophilic and halotolerant microorganisms occur by pathways similar to those found in non-halophiles.

  11. Polycyclic Aromatic Hydrocarbons: Are They a Problem in Processed Oil Shales?

    OpenAIRE

    Maase, David L.; Adams, V. Dean

    1983-01-01

    Organic residues from processed oil shales were characterisized with specific attention to polycyclic aromatic hydrocarbons (PAH). Oil shale development in the White River Basin (Utah and Colorado) was projected and hydrological and geological parameters pertinent to estimations of polycyclic aromatic hydrocarbons (PAH) flux were focused. Oil shale samples from the Union B, Paraho, and Tosco II processes were extr...

  12. Fate and degradation of petroleum hydrocarbons in stormwater bioretention cells

    Science.gov (United States)

    LeFevre, Gregory Hallett

    This dissertation describes the investigation of the fate of hydrocarbons in stormwater bioretention areas and those mechanisms that affect hydrocarbon fate in such systems. Seventy-five samples from 58 bioretention areas were collected and analyzed to measure total petroleum hydrocarbon (TPH) residual and biodegradation functional genes. TPH residual in bioretention areas was greater than background sites but low overall (<3 µg/kg), and well below either the TPH concentration of concern or the expected concentration, assuming no losses. Bioretention areas with deep-root vegetation contained significantly greater quantites of bacterial 16S rRNA genes and two functional genes involved in hydrocarbon biodegradation. Field soils were capable of mineralizing naphthalene, a polycyclic aromatic hydrocarbon (PAH) when incubated in the laboratory. In an additional laboratory investigation, a column study was initiated to comprehensively determine naphthalene fate in a simulated bioretention cell using a 14C-labeled tracer. Sorption to soil was the greatest sink of naphthalene in the columns, although biodegradation and vegetative uptake were also important loss mechanisms. Little leaching occurred following the first flush, and volatilization was insignificant. Significant enrichment of naphthalene degrading bacteria occurred over the course of the experiment as a result of naphthalene exposure. This was evident from enhanced naphthalene biodegradation kinetics (measured via batch tests), significant increases in naphthalene dioxygenase gene quantities, and a significant correlation observed between naphthalene residual and biodegradation functional genes. Vegetated columns outperformed the unplanted control column in terms of total naphthalene removal and biodegradation kinetics. As a result of these experiments, a final study focused on why planted systems outperform unplanted systems was conducted. Plant root exudates were harvested from hydroponic setups for three

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

    OpenAIRE

    Nielsen, R. Brent; Jay D Keasling

    1997-01-01

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

  14. Biodegradation of polycyclic aromatic hydrocarbons by Trichoderma species: a mini review.

    Science.gov (United States)

    Zafra, German; Cortés-Espinosa, Diana V

    2015-12-01

    Fungi belonging to Trichoderma genus are ascomycetes found in soils worldwide. Trichoderma has been studied in relation to diverse biotechnological applications and are known as successful colonizers of their common habitats. Members of this genus have been well described as effective biocontrol organisms through the production of secondary metabolites with potential applications as new antibiotics. Even though members of Trichoderma are commonly used for the commercial production of lytic enzymes, as a biological control agent, and also in the food industry, their use in xenobiotic biodegradation is limited. Trichoderma stands out as a genus with a great range of substrate utilization, a high production of antimicrobial compounds, and its ability for environmental opportunism. In this review, we focused on the recent advances in the research of Trichoderma species as potent and efficient aromatic hydrocarbon-degrading organisms, as well as aimed to provide insight into its potential role in the bioremediation of soils contaminated with heavy hydrocarbons. Several Trichoderma species are associated with the ability to metabolize a variety of both high and low molecular weight polycyclic aromatic hydrocarbons (PAHs) such as naphthalene, phenanthrene, chrysene, pyrene, and benzo[a]pyrene. PAH-degrading species include Trichoderma hamatum, Trichoderma harzianum, Trichoderma reesei, Trichoderma koningii, Trichoderma viride, Trichoderma virens, and Trichoderma asperellum using alternate enzyme systems commonly seen in other organisms, such as multicooper laccases, peroxidases, and ring-cleavage dioxygenases. Within these species, T. asperellum stands out as a versatile organism with remarkable degrading abilities, high tolerance, and a remarkable potential to be used as a remediation agent in polluted soils.

  15. Biodegradation of polycyclic aromatic hydrocarbons by Trichoderma species: a mini review.

    Science.gov (United States)

    Zafra, German; Cortés-Espinosa, Diana V

    2015-12-01

    Fungi belonging to Trichoderma genus are ascomycetes found in soils worldwide. Trichoderma has been studied in relation to diverse biotechnological applications and are known as successful colonizers of their common habitats. Members of this genus have been well described as effective biocontrol organisms through the production of secondary metabolites with potential applications as new antibiotics. Even though members of Trichoderma are commonly used for the commercial production of lytic enzymes, as a biological control agent, and also in the food industry, their use in xenobiotic biodegradation is limited. Trichoderma stands out as a genus with a great range of substrate utilization, a high production of antimicrobial compounds, and its ability for environmental opportunism. In this review, we focused on the recent advances in the research of Trichoderma species as potent and efficient aromatic hydrocarbon-degrading organisms, as well as aimed to provide insight into its potential role in the bioremediation of soils contaminated with heavy hydrocarbons. Several Trichoderma species are associated with the ability to metabolize a variety of both high and low molecular weight polycyclic aromatic hydrocarbons (PAHs) such as naphthalene, phenanthrene, chrysene, pyrene, and benzo[a]pyrene. PAH-degrading species include Trichoderma hamatum, Trichoderma harzianum, Trichoderma reesei, Trichoderma koningii, Trichoderma viride, Trichoderma virens, and Trichoderma asperellum using alternate enzyme systems commonly seen in other organisms, such as multicooper laccases, peroxidases, and ring-cleavage dioxygenases. Within these species, T. asperellum stands out as a versatile organism with remarkable degrading abilities, high tolerance, and a remarkable potential to be used as a remediation agent in polluted soils. PMID:26498812

  16. Ectomycorrhizas impede phytoremediation of polycyclic aromatic hydrocarbons (PAHs) both within and beyond the rhizosphere

    Energy Technology Data Exchange (ETDEWEB)

    Joner, Erik J. [Laboratoire des Interactions Microorganismes-Mineraux-Matiere Organique dans les Sols (LIMOS), Universite H. Poincare Nancy 1, P.O. Box 239, F-54506 Vandoeuvre-les-Nancy (France)]. E-mail: erik.joner@jordforsk.no; Leyval, Corinne [Laboratoire des Interactions Microorganismes-Mineraux-Matiere Organique dans les Sols (LIMOS), Universite H. Poincare Nancy 1, P.O. Box 239, F-54506 Vandoeuvre-les-Nancy (France); Colpaert, Jan V. [Centre for Environmental Sciences, Environmental Biology Group, Hasselt University, Agoralaan, Gebouw D, B-3590 Diepenbeek (Belgium)

    2006-07-15

    Exploitation of mycorrhizas to enhance phytoremediation of organic pollutants has received attention recently due to their positive effects on establishment of plants in polluted soils. Some evidence exist that ectomycorrhizas enhance the degradation of pollutants of low recalcitrance, while less easily degradable polyaromatic molecules have been degraded only by some of these fungi in vitro. Natural polyaromatic (humic) substances are degraded more slowly in soil where ectomycorrhizal fungi are present, thus phytoremediation of recalcitrant pollutants may not benefit from the presence of these fungi. Using a soil spiked with three polycyclic aromatic hydrocarbons (PAHs) and an industrially polluted soil (1 g kg{sup -1} of {sigma}12 PAHs), we show that the ectomycorrhizal fungus Suillus bovinus, forming hydrophobic mycelium in soil that would easily enter into contact with hydrophobic pollutants, impedes rather than promotes PAH degradation. This result is likely to be a nutrient depletion effect caused by fungal scavenging of mineral nutrients. - The ectomycorrhizal fungus S. bovinus impeded degradation of PAHs in soil, probably due to its negative effect on the availability of mineral nutrients of more potent PAH degraders.

  17. Ectomycorrhizas impede phytoremediation of polycyclic aromatic hydrocarbons (PAHs) both within and beyond the rhizosphere

    International Nuclear Information System (INIS)

    Exploitation of mycorrhizas to enhance phytoremediation of organic pollutants has received attention recently due to their positive effects on establishment of plants in polluted soils. Some evidence exist that ectomycorrhizas enhance the degradation of pollutants of low recalcitrance, while less easily degradable polyaromatic molecules have been degraded only by some of these fungi in vitro. Natural polyaromatic (humic) substances are degraded more slowly in soil where ectomycorrhizal fungi are present, thus phytoremediation of recalcitrant pollutants may not benefit from the presence of these fungi. Using a soil spiked with three polycyclic aromatic hydrocarbons (PAHs) and an industrially polluted soil (1 g kg-1 of Σ12 PAHs), we show that the ectomycorrhizal fungus Suillus bovinus, forming hydrophobic mycelium in soil that would easily enter into contact with hydrophobic pollutants, impedes rather than promotes PAH degradation. This result is likely to be a nutrient depletion effect caused by fungal scavenging of mineral nutrients. - The ectomycorrhizal fungus S. bovinus impeded degradation of PAHs in soil, probably due to its negative effect on the availability of mineral nutrients of more potent PAH degraders

  18. Role of methyl group number on SOA formation from monocyclic aromatic hydrocarbons photooxidation under low-NOx conditions

    OpenAIRE

    Li, L.; Tang, P.; Nakao, S.; Chen, C.-L.; Cocker III, D. R.

    2016-01-01

    Substitution of methyl groups onto the aromatic ring determines the secondary organic aerosol (SOA) formation from the monocyclic aromatic hydrocarbon precursor (SOA yield and chemical composition). This study links the number of methyl groups on the aromatic ring to SOA formation from monocyclic aromatic hydrocarbons photooxidation under low-NOx conditions (HC/NO  >  10 ppbC : ppb). Monocyclic aromatic hydrocarbons with increasing numbers of methyl groups are systemat...

  19. [Enhanced bioremediation of coking plant soils contaminated with polycyclic aromatic hydrocarbons].

    Science.gov (United States)

    Lu, Xiao-Xia; Li, Xiu-Li; Ma, Jie; Wu, Shu-Ke; Chen, Chao-Qi; Wu, Wei

    2011-03-01

    Soil samples contaminated with polycyclic aromatic hydrocarbons (PAHs) were collected from Beijing Coking Plant. The purposes were to isolate PAHs degrading bacteria from the soils, determine their appropriate living condition, enrich them and apply them in the enhanced bioremediation of the contaminated soils. Using each of the 16 USEPA priority PAHs as the sole carbon source, PAHs degrading bacteria were isolated using the method of plate streaking and identified by genetic analysis. In total seven species of PAHs degrading bacteria were obtained. When mixed, these bacteria could degrade the 16 (2-6 cyclic) PAHs studied at appropriate concentrations. In the liquid medium, when the total concentration of the 16 PAHs (sigma PAH16) was 17 microg/mL, single bacteria could grow well and degrade the PAHs. However, when sigma PAH16 was 166 microg/mL, the growth and activity of either single PAHs degrading bacteria or a mixture of the seven PAHs degrading bacteria were inhibited. Aiming at the contaminated soils from Beijing coking plant, five treatments were performed, i.e., control (C), addition of nutrient (N), addition of nutrient and PAHs degrading bacteria (N + B), addition of nutrient and surfactant (N +S), addition of nutrient and PAHs degrading bacteria and surfactant (N + B + S). After five weeks of experiment, compared to the C treatment, the mean removal rate of the 16 PAHs in the N + B treatment was increased 32%, and the mean removal rate of the 16 PAHs in the N + B + S treatment was increased 46% (the mean removal rate of the 10 4-6 cyclic PAHs was increased 52%). The addition of PAHs degrading bacteria and surfactant could significantly enhance the degradation of PAHs in the soils. This study provides evidence for the enhanced bioremediation of PAHs contaminated soil for Beijing coking plant and other coking plants.

  20. Formation History of Polycyclic Aromatic Hydrocarbons in Galaxies

    CERN Document Server

    Seok, Ji Yeon; Asano, Ryosuke S

    2014-01-01

    Polycyclic aromatic hydrocarbons (PAHs) are some of the major dust components in the interstellar medium (ISM). We present our evolution models for the abundance of PAHs in the ISM on a galaxy-evolution timescale. We consider shattering of carbonaceous dust grains in interstellar turbulence as the formation mechanism of PAHs while the PAH abundance can be reduced by coagulation onto dust grains, destruction by supernova shocks, and incorporation into stars. We implement these processes in a one-zone chemical evolution model to obtain the evolution of the PAH abundance in a galaxy. We find that PAH formation becomes accelerated above certain metallicity where shattering becomes efficient. For PAH destruction, while supernova shock is the primary mechanism in the metal-poor environment, coagulation is dominant in the metal-rich environment. We compare the evolution of the PAH abundances in our models with observed abundances in galaxies with a wide metallicity range. Our models reproduce both the paucity of PAH...

  1. Polycyclic aromatic hydrocarbons in sediments of China Sea.

    Science.gov (United States)

    Li, Yanxia; Duan, Xiaoyong

    2015-10-01

    Increasing pollution pressures were placed in the coastal and estuarine ecosystems in China because of the elevated pollutants discharged from various sources. Polycyclic aromatic hydrocarbons (PAHs) in the environment were closely linked to human activities, which have been intensively studied for their geochemical interest as markers. In this review, the status of PAH contamination in China Sea was assessed by comprehensive reviews of the concentrations, sources, and fates of PAHs in sediments of China Sea. PAH concentrations in China Sea sediments decreased from north to south due to the higher emissions in North China. Atmosphere was probably the main carrier of PAHs in the north due to the higher contents of atmospheric fine particles and higher wind speeds. However, riverine inputs were probably the most important sources of PAHs in the coastal sediments of South China due to higher rainfall.

  2. Polycyclic aromatic hydrocarbons' formation and occurrence in processed food.

    Science.gov (United States)

    Singh, Lochan; Varshney, Jay G; Agarwal, Tripti

    2016-05-15

    Polycyclic aromatic hydrocarbons (PAHs) emerged as an important contaminant group in a gamut of processed food groups like dairy, nuts, herbs, beverages, meat products etc. Different cooking processes and processing techniques like roasting, barbecuing, grilling, smoking, heating, drying, baking, ohmic-infrared cooking etc. contribute towards its formation. The level of PAHs depends on factors like distance from heat source, fuel used, level of processing, cooking durations and methods, whereas processes like reuse, conching, concentration, crushing and storage enhance the amount of PAHs in some food items. This review paper provides insight into the impact of dietary intake of PAHs, its levels and formation mechanism in processed food items and possible interventions for prevention and reduction of the PAHs contamination. The gaps and future prospects have also been assessed.

  3. Polycyclic aromatic hydrocarbons' formation and occurrence in processed food.

    Science.gov (United States)

    Singh, Lochan; Varshney, Jay G; Agarwal, Tripti

    2016-05-15

    Polycyclic aromatic hydrocarbons (PAHs) emerged as an important contaminant group in a gamut of processed food groups like dairy, nuts, herbs, beverages, meat products etc. Different cooking processes and processing techniques like roasting, barbecuing, grilling, smoking, heating, drying, baking, ohmic-infrared cooking etc. contribute towards its formation. The level of PAHs depends on factors like distance from heat source, fuel used, level of processing, cooking durations and methods, whereas processes like reuse, conching, concentration, crushing and storage enhance the amount of PAHs in some food items. This review paper provides insight into the impact of dietary intake of PAHs, its levels and formation mechanism in processed food items and possible interventions for prevention and reduction of the PAHs contamination. The gaps and future prospects have also been assessed. PMID:26776034

  4. [Polycyclic aromatic hydrocarbons (PAH) in cereal breakfast products].

    Science.gov (United States)

    Ciemniak, Artur; Chrachol, Lucyna

    2008-01-01

    Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous pollutants formed by incomplete combustion (pyrolysis) of several organic materials. PAHs occur as complex mixtures, never as individual components. They are chemically stable and highly lipophilic in nature and occur as contaminants in different food categories: vegetables, fruit, cereals, oils and fats, especially barbecued and smoked food. The present study was carried out to determine 16 PAHs in cereal products: musli, corn, oats and barley flakes, and crunchy. The analytical procedure was based on alkaline digestion, extraction with n-hexane and cleaned up in a florisil cartridge. Chromatographic separation was performed using gas chromatography (HP 6890) coupled to mass spectrometry (HP 5973). The levels of PAHs in most samples were generally low and excepting one sample of bred varied between 4.2 to 169 microg/kg. Benzo[a]pyrene, was detected in all samples, at level 0.02 microg/kg to 16 microg/kg. PMID:19143427

  5. Polycyclic aromatic hydrocarbons in cereal products on the Turkish market.

    Science.gov (United States)

    Kacmaz, Sibel

    2016-09-01

    The contamination level of four EU marker polycyclic aromatic hydrocarbons (PAHs) in some cereal-derived products was surveyed in this study. Thirty-eight samples, 20 bread and 18 breakfast cereals, were purchased from retail shops and local markets of East Black sea region in Turkey. The samples were analysed for four EU marker PAHs, using ultrasonic extraction, solid-phase extraction (SPE) clean up and stable-isotope dilution gas chromatography with mass-spectrometric (GC/MS) detection. The method was validated with the parameters linearity, accuracy, precision, limit of detection (LOD), limit of quantitation (LOQ) and uncertainty. Total content of the four PAHs in bread varied from 0.19 to 0.46 µg kg(-1) and in breakfast cereals from 0.10 to 0.87 µg kg(-1). PMID:26986946

  6. A Shape-Persistent Cryptand for Capturing Polycyclic Aromatic Hydrocarbons.

    Science.gov (United States)

    Zhang, Rui-Feng; Hu, Wen-Jing; Liu, Yahu A; Zhao, Xiao-Li; Li, Jiu-Sheng; Jiang, Biao; Wen, Ke

    2016-07-01

    A shape-persistent cryptand 1, containing two face-to-face oriented electron-deficient 2,4,6-triphenyl-1,3,5-triazine units separated by approximately 7 Å, and bridged by two rigid 1,8-naphthyridine linkers and a pentaethylene oxide loop, is created for capturing polycyclic aromatic hydrocarbons. Cryptand 1 formed 1:1 complexes with PAH guest molecules, such as phenanthrene (6), anthracene (7), pyrene (8), triphenylene (9), and tetraphene (10). The single-crystal structure of complex 6⊂1 revealed that 6 was included in the cavity of 1 via face-to-face π···π stacking interactions. Soaking crystalline 1 in a toluene solution of anthracene resulted in anthracene from the toluene solution being picked up by the crystalline solid of 1. PMID:27258531

  7. Magnetic instability and pair binding in aromatic hydrocarbon superconductors

    Science.gov (United States)

    Huang, Zhongbing; Zhang, Chao; Lin, Hai-Qing

    2012-01-01

    Understanding magnetism and electron correlation in many unconventional superconductors is essential to explore mechanism of superconductivity. In this work, we perform a systematic numerical study of the magnetic and pair binding properties in recently discovered polycyclic aromatic hydrocarbon (PAH) superconductors including alkali-metal-doped picene, coronene, phenanthrene, and dibenzopentacene. The π-electrons on the carbon atoms of a single molecule are modelled by the one-orbital Hubbard model, and the energy difference between carbon atoms with and without hydrogen bonds is taking into account. We demonstrate that the spin polarized ground state is realized for charged molecules in the physical parameter regions, which provides a reasonable explanation of local spins observed in PAHs. In alkali-metal-doped dibenzopentacene, our results show that electron correlation may produce an effective attraction between electrons for the charged molecule with one or three added electrons. PMID:23213358

  8. Study on Aromatization of C6 Aliphatic Hydrocarbons on ZRP Zeolite Catalyst

    Institute of Scientific and Technical Information of China (English)

    Wang Yongjun; Xie Chaogang

    2004-01-01

    The performance of ZRP zeolite catalysts for aromatization of C6 aliphatic hydrocarbons was investigated in a pulsed microreactor. The influence of metal modified ZRP zeolites on aromatization reaction was also studied, coupled with comparison of aromatization tendencies of olefins, paraffins and paraffins with different degrees of chain branching. Test results had shown that the lower the silicon/aluminum ratio in the ZRP zeolite, the higher the aromatization reactivity of aliphatic hydrocarbons. Modification of ZRP zeolite by zinc and its zinc content had apparent impact on the yield and distribution of aromatics. The aromatization tendency of olefins was apparently better than paraffins, while the aromatization tendency of monomethyl paraffins was better than that of straight-chain paraffins with the exception of dimethyl paraffins, which had worse aromatization tendency because of their steric hindrance.

  9. Exposure to polycyclic aromatic hydrocarbons with special focus on cancer

    Institute of Scientific and Technical Information of China (English)

    Thamaraiselvan; Rengarajan; Peramaiyan; Rajendran; Natarajan; Nandakumar; Boopathy; Lokeshkumar; Palaniswami; Rajendran; Ikuo; Nishigaki

    2015-01-01

    Polycyclie aromatic hydrocarbons(PAHs) are a group of compounds consisting of two or more fused aromatic rings.Most of them are formed during incomplete combustion of organic materials such as wood and fossil fuels,petroleum products,and coal.The composition of PAH mixtures varies with the source and is also affected by selective weathering effects in the environment.PAHs are ubiquitous pollutants frequently found in a variety of environments such as fresh water and marine sediments,the atmosphere,and ice.Due to their widespread distribution,the environmental pollution due to PAHs has aroused global concern.Many PAHs and their epoxides are highly toxic,mutagenic and/or carcinogenic to microorganisms as well as to higher forms of life including humans.The main aim of this review is to provide contemporary information on PAH sources,route of exposure,worldwide emission rate,and adverse effects on humans,especially with reference to cancer.

  10. Alkyl polycyclic aromatic hydrocarbons emissions in diesel/biodiesel exhaust

    Science.gov (United States)

    Casal, Carina S.; Arbilla, Graciela; Corrêa, Sergio M.

    2014-10-01

    Polycyclic aromatic hydrocarbons (PAHs) are widely studied in environmental matrices, such as air, water, soil and sediment, because of their toxicity, mutagenicity and carcinogenicity. Because of these properties, the environmental agencies of developed countries have listed sixteen PAHs as priority pollutants. Few countries have limits for these compounds for ambient air, but they only limit emissions from stationary and mobile sources and occupational areas. There are several studies to specifically address the 16 priority PAHs and very little for the alkyl PAHs. These compounds are more abundant, more persistent and frequently more toxic than the non-alkylated PAHs, and the toxicity increases with the number of alkyl substitutions on the aromatic ring. In this study, a method was developed for the analysis of PAHs and alkyl PAHs by using a GC-MS and large injection volume injection coupled with program temperature vaporisation, which allows for limits of detection below 1.0 ng μL-1. Several variables were tested, such as the injection volume, injection velocity, injector initial temperature, duration of the solvent split and others. This method was evaluated in samples from particulate matter from the emissions of engines employing standard diesel, commercial diesel and biodiesel B20. Samples were collected on a dynamometer bench for a diesel engine cycle and the results ranged from 0.5 to 96.9 ng mL-1, indicating that diesel/biodiesel makes a significant contribution to the formation of PAHs and alkyl PAHs.

  11. Accumulation of Trace Metals, Petroleum Hydrocarbons, and Polycyclic Aromatic Hydrocarbons in Marine Copepods from the Arabian Gulf

    OpenAIRE

    El-Din, N.M. Nour; Abdel-Moati, M. A. R.

    2001-01-01

    In this study, zooplankton samples were collected from the coastal waters of Qatar during winter and summer 1998 to assess the impact of growing industrialization on the bioaccumulation of trace metals, total petroleum hydrocarbons (TPHCs) and polycyclic aromatic hydrocarbons (PAHs) in copepods, the dominant zooplankton group and main food for fish in the Arabian Gulf.

  12. Inhibitory effects of polycyclic aromatic hydrocarbons (PAHs) on photosynthetic performance are not related to their aromaticity.

    Science.gov (United States)

    Jajoo, Anjana; Mekala, Nageswara Rao; Tomar, Rupal Singh; Grieco, Michele; Tikkanen, Mikko; Aro, Eva-Mari

    2014-08-01

    Polycyclic aromatic hydrocarbons (PAHs) are very toxic and highly persistent environmental pollutants which accumulate in soil and affect growth of the plants adversely. This study aims to investigate inhibitory effects of 3 major PAH particularly on photosynthetic processes in Arabidopsis thaliana grown in soil treated with PAH. The 3 PAH chosen differ from each other in aromaticity (number of rings) comprising their structure (2 rings: naphthalene, 3 rings: anthracene and 4 rings: pyrene). Several growth parameters and Chlorophyll a fluorescence was monitored in PAH treated plants. BN-PAGe analysis was done in order to get information about change in the protein conformation. PAH treatment led to increased value of Fo which collaborated with increase in the amount of free LHC as seen through BN-Page analysis. Thus PAH were found to inhibit PS II photochemistry and caused distinct change in pigment composition. However the results led us to infer that 3-ring anthracence is more inhibitory as compared to 2-ring naphthalene and 4-ring pyrene. This indicates that aromaticity of PAH is unrelated to their response on photosynthetic processes.

  13. Oxidation of polycyclic aromatic hydrocarbons using partially purified laccase from residual compost of agaricus bisporus

    Energy Technology Data Exchange (ETDEWEB)

    Mayolo-Deloisa, K. [Center for Biotechnology Research, Autonomous University of Morelos State, Cuernavaca, Morelos (Mexico); Center for Biotechnology-FEMSA, Monterrey Institute of Technology, Campus Monterrey, Monterrey (Mexico); Machin-Ramirez, C. [Center for Biotechnology Research, Autonomous University of Morelos State, Cuernavaca, Morelos (Mexico); Faculty of Chemical Sciences and Engineering, Autonomous University of Morelos State, Cuernavaca, Morelos (Mexico); Rito-Palomares, M. [Center for Biotechnology-FEMSA, Monterrey Institute of Technology, Campus Monterrey, Monterrey (Mexico); Trejo-Hernandez, M.R. [Center for Biotechnology Research, Autonomous University of Morelos State, Cuernavaca, Morelos (Mexico)

    2011-08-15

    Laccase partially purified from residual compost of Agaricus bisporus by an aqueous two-phase system (Lac ATPS) was used in degrading polycyclic aromatic hydrocarbons: fluorene (Flu), phenanthrene (Phe), anthracene (Ant), benzo[a]pyrene (BaP), and benzo[a]anthracene (BaA). The capacity of the enzyme to oxidize polyaromatic compounds was compared to that of the crude laccase extract (CE). After treatment of 72 h, Lac ATPS and CE were not capable of oxidizing Flu and Phe, while Ant, BaP, and BaA were oxidized, resulting in percentages of oxidation of 11.2 {+-} 1, 26 {+-} 2, and 11.7 {+-} 4 % with CE, respectively. When Lac ATPS was used, the following percentages of oxidation were obtained: 11.4 {+-} 3 % for Ant, 34 {+-} 0.1 % for BaP, and 13.6 {+-} 2 % for BaA. The results reported here demonstrate the potential application of Lac ATPS for the oxidation of polycyclic aromatic hydrocarbons. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  14. Biodegradation of polycyclic aromatic hydrocarbons in sediments from the Daliao River watershed, China

    Institute of Scientific and Technical Information of China (English)

    QUAN Xiangchun; TANG Qian; HE Mengchang; YANG Zhifeng; LIN Chunye; GUO Wei

    2009-01-01

    The Daliao River, as an important water system in Northeast China, was reported to be heavily polluted by polycyclic aromatic hydrocarbons (PAHs). Aerobic biodegradations of four selected PAHs (naphthalene, phenanthrene, fluorene and anthracene) alone or in their mixture in fiver sediments from the Daliao River water systems were studied in microcosm systems. Effects of additional carbon source, inorganic nitrogen and phosphorus, temperature variation on PAHs degradation were also investigated. Results showed that the degradation of phenanthrene in water alone system was faster than that in water-sediment combined system. Degradation of phenanthrene in sediment was enhanced by adding yeast extract and ammonium, but retarded by adding sodium acetate and not significantly influenced by adding phosphate. Although PAHs could also be biodegraded in sediment under low temperature (5℃), much lower degradation rate was observed. Sediments from the three main streams of the Daliao River water system (the Hun River, the Taizi River and the Daliao River) demonstrated different degradation capacities and patterns to four PAHs. Average removal rates (15 or 19 d) of naphthalene, phenanthrene, fluorene and anthracene by sediment were in the range of 0.062-0.087, 0.005-0.066, 0.008-one. In multiple PAHs systems, the interactions between PAHs influenced each PAH biodegradation.

  15. Polycyclic aromatic hydrocarbon biodegradation and extracellular enzyme secretion in agitated and stationary cultures of Phanerochaete chrysosporium

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    The extracellular enzyme secretion and biodegradation of polycyclic aromatic hydrocarbons (PAHs) were studied in agitated and shallow stationary liquid cultures of Phanerochaete chrysosporium. Veratryl alcohol and Tween80 were added to cultures as lignin peroxidase (LiP) and manganese peroxidase (MnP) inducer, respectively. Shallow stationary cultures were suitable for the production of enzyme, whereas agitated cultures enhanced overall biodegradation by facilitating interphase mass transfer of PAH into aqueous phases. The use of a LiP stimulator, veratryl alcohol, did not increase PAH degradation but significantly enhanced LiP activity. In contrast, Tween80 increased both MnP secretion and PAH degradation in shallow stationary cultures. On the other hand, high PAH degradation was observed in agitated cultures in the absence of detectable LiP and MnP activities. The results suggested that extracellular peroxidase activities are not directly related to the PAH degradation, and the increased solubility rather than enzyme activity may be more important in the promotion of PAH degradation.

  16. Bioremediation a potential approach for soil contaminated with polycyclic aromatic hydrocarbons: An Overview

    Directory of Open Access Journals (Sweden)

    Norzila Othman

    2011-12-01

    Full Text Available Polycyclic aromatic hydrocarbons (PAHs represent a group of priority pollutants which are present at high concentration in soils of many industrially contaminated sites. Standards and criteria for the remediation of soils contaminated with PAHs vary widely between countries. Bioremediation has gained preference as a technology for remediation contaminated sites as it is less expensive and more environmental friendly. Bioremediation utilizes microorganisms to degrade PAHs to less toxic compounds. This technology degrades contaminants through natural biodegradation mechanisms or enhanced biodegradation mechanism and can be performed in-situ or ex-situ under aerobic or anaerobic conditions. The purpose of this paper is to highlight potential of using isolated strains from municipal sludge on soil remediation. Several indigenous bacteria from municipal sludge namely genus Micrococus, Sphingomonas, and Corynebacterium demonstrated a high removal rate of PAHs with more than 80% of lower molecular weight of PAHs degraded after one week incubation. Laboratory studies had established that these genus able to degrade PAHs on contaminated soil. The successful application of bacteria to the bioremediation of PAHs contaminated sites requires a deeper understanding of how microbial PAH degradation proceeds. An overview of research focusing on biodegradation of PAHs will be presented.

  17. Identification and discrimination of polycyclic aromatic hydrocarbons using Raman spectroscopy

    Science.gov (United States)

    Cloutis, Edward; Szymanski, Paul; Applin, Daniel; Goltz, Douglas

    2016-08-01

    Polycyclic aromatic hydrocarbons (PAHs) are widely present throughout the Solar System and beyond. They have been implicated as a contributor to unidentified infrared emission bands in the interstellar medium, comprise a substantial portion of the insoluble organic matter in carbonaceous chondrites, are expected stable components of organic matter on Mars, and are present in a wide range of terrestrial hydrocarbons and as components of biomolecules. However, PAH structures can be very complicated, making their identification challenging. Raman spectroscopy is known to be especially sensitive to the highly polarizable C-C and C=C bonds found in PAHs, and therefore, can be a powerful tool for PAH structural and compositional elucidation. This study examined Raman spectra of 48 different PAHs to determine the degree to which Raman spectroscopy could be used to uniquely identify different species, factors that control the positions of major Raman peaks, the degree to which induced fluorescence affects the intensity of Raman peaks, its usefulness for PAH discrimination, and the effects of varying excitation wavelength on some PAH Raman spectra. It was found that the arrangement and composition of phenyl (benzene) rings, and the type and position of functional groups can greatly affect fluorescence, positions and intensities of Raman peaks associated with the PAH backbone, and the introduction of new Raman peaks. Among the functional groups found on many of the PAHs that were analyzed, only a few Raman peaks corresponding to the molecular vibrations of these groups could be clearly distinguished. Comparison of the PAH Raman spectra that were acquired with both 532 and 785 nm excitation found that the longer wavelength resulted in reduced fluorescence, consistent with previous studies.

  18. The Exobiological Role of Interstellar Polycyclic Aromatic Hydrocarbons and Ices

    Science.gov (United States)

    Hudgins, Douglas M.; DeVincenzi, Donald (Technical Monitor)

    2002-01-01

    Tremendous strides have been made in our understanding of interstellar material over the past twenty years thanks to significant, parallel developments in observational astronomy and laboratory astrophysics. Before this time, the composition of interstellar dust was largely guessed-at, the presence of ices in interstellar clouds ignored, and the notion that large, gas phase, carbon rich molecules might be abundant and widespread throughout the interstellar medium (ISM) considered impossible. Today, the composition of dust in the ISM is reasonably well constrained to micron-sized cold refractory materials comprised of amorphous and crystalline silicates mixed with an amorphous carbonaceous material containing aromatic structural units and short, branched aliphatic chains. Shrouded within the protective confines of cold, opaque molecular clouds--the birthplace of stars and planets--these cold dust particles secrete mantles of mixed molecular ices whose compositions are also well constrained. Finally, amidst the molecular inventory of these ice mantles are likely to be found polycyclic aromatic hydrocarbons (PAHs), shockingly large molecules by the standards of interstellar chemistry, the telltale infrared spectral signature of which is now recognized throughout the Universe. In the first part of this talk, we will review the spectroscopic evidence that forms the basis for the currently accepted abundance and ubiquity of PANs in the ISM. We will then look at a few specific examples which illustrate how experimental and theoretical data can be applied to interpret the interstellar spectra and track how the PAN population evolves as it passes from its formation site in the circumstellar outflows of dying stars, through the various phases of the ISM, and into forniing planetary systems. Nevertheless, despite the fact that PANs likely represent the single largest molecular reservoir of organic carbon in evolving planetary systems, they are not what would be considered

  19. Molecular catalytic hydrogenation of aromatic hydrocarbons and hydrotreating of coal liquids.

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Shiyong; Stock, L.M.

    1996-05-01

    This report presents the results of research on the development of new catalytic pathways for the hydrogenation of multiring aromatic hydrocarbons and the hydrotreating of coal liquids at The University of Chicago under DOE Contract No. DE-AC22-91PC91056. The work, which is described in three parts, is primarily concerned with the research on the development of new catalytic systems for the hydrogenation of aromatic hydrocarbons and for the improvement of the quality of coal liquids by the addition of dihydrogen. Part A discusses the activation of dihydrogen by very basic molecular reagents to form adducts that can facilitate the reduction of multiring aromatic hydrocarbons. Part B examines the hydrotreating of coal liquids catalyzed by the same base-activated dihydrogen complexes. Part C concerns studies of molecular organometallic catalysts for the hydrogenation of monocyclic aromatic hydrocarbons under mild conditions.

  20. Identification of persulfate oxidation products of polycyclic aromatic hydrocarbon during remediation of contaminated soil

    Science.gov (United States)

    The extent of PAH transformation, the formation and transformation of reaction byproducts during persulfate oxidation of polycyclic aromatic hydrocarbons (PAHs) in coking plant soil was investigated. Pre-oxidation analyses indicated that oxygen-containing PAHs (oxy-PAHs) existed ...

  1. Compost-mediated removal of polycyclic aromatic hydrocarbons from contaminated soil.

    Science.gov (United States)

    Sasek, V; Bhatt, M; Cajthaml, T; Malachová, K; Lednická, D

    2003-04-01

    Compost-assisted remediation of a manufactured-gas plant soil contaminated with polycyclic aromatic hydrocarbons (PAHs) was performed in thermally insulated composting chamber using mushroom compost consisting wheat straw, chicken manure, and gypsum. The degradation of individual PAHs was in range of 20-60% at the end of 54 days of composting followed by further increase of PAH removal (37-80%) after another 100 days of maturation. Both chemical analysis of the contaminated soil for PAHs and ecotoxicity tests on bioluminescent bacteria, earthworms, and plant seeds were performed before and after the composting. After the composting, inhibition of bioluminescence decreased, whereas no significant change in toxicity was observed for earthworm survival and seed germination. Using bacterial culture of Escherichia coli K12 genotoxicity tests were performed on samples taken from different parts of the composting pile; after the composting the decrease in genotoxicity was observed only in the sample taken from upper part of the composted pile.

  2. Evaluating emission levels of polycyclic aromatic hydrocarbons from organic materials by analytical pyrolysis

    Energy Technology Data Exchange (ETDEWEB)

    Fabbri, Daniele; Vassura, Ivano [Laboratory of Chemistry, C.I.R.S.A., University of Bologna, via S. Alberto 163, I-48100 Ravenna (Italy)

    2006-03-01

    A procedure in off-line analytical pyrolysis was investigated for the rapid determination of polycyclic aromatic hydrocarbons (PAHs) evolved from thermal degradation of organic materials. Samples spiked with perdeuterated PAHs were pyrolysed at 1000{sup o}C for 60s by means of a resistively heated filament pyrolyser inserted into a glass chamber connected to a cartridge with a sorbent (XAD-2 resin). PAHs trapped onto the resin were extracted with dichloromethane and analysed by gas chromatography-mass spectrometry (GC-MS). The analytical performance of the overall procedure (precision, recovery, effect of experimental parameters) was evaluated by pyrolysing a bituminous coal certified reference material (CRM). Emission levels of naphthalene, 1-methylnaphthalene, 2-methylnaphthalene, acenaphtylene, acenaphthene, fluorene, phenanthrene, anthracene, fluoranthene, pyrene were determined for bituminous and anthracite coals, tyre, and cellulose. Despite some limitations, the method was adequate to the purpose of quantitatively measuring the tendency of various materials to release volatile PAHs upon heating. (author)

  3. MONITORING POLYNUCLEAR AROMATIC HYDROCARBONS IN SEDIMENT POREWATER BY SPMD

    Institute of Scientific and Technical Information of China (English)

    朱亚先; 张勇; 庄一廷; Ka-FaiPoon; MichaelH.W.Lam; 洪华生; RudolfS.S.Wu

    2001-01-01

    A new mimic biological Semi-permeable Membrane Device (SPMD) introduced for sampling organic pollutants yielded satisfactory results when it was frrst used as a passive sampler to concentrate and determine 16 kinds of polynuclear aromatic hydrocarbons (PAHs) by means of capillary GC on an HP 5890 GC-FID in coastal sediment perewater. The concentration of PAHs in sediment porewater for naphthalene(N), acenaphthlene(AL), acenaphthene (AE), fluorene (F), phenaphthene(P), anthracene(A), fluoranthene(FA), pyrene(Py), benzo[a]anthracene(B[a]A), chrysene(Chr), benzo[b] fluor- anthene(B[b]F), benzo[k]fluoranthene(B[k]F), benzo[a]pyrene(B[a]P),indeno[1,2,3,-cd]-Pyrene(I[123]P), dibenz[a,h]anthracene(D[ab]A) and benzo[g,h,i] perylene(B[ghi]P) were:50.36, under detection limits(UD), 18.19, 8.41, 8.40, 1.44, UD, 8.01, 524.15, 168.47, 50.13,123.66, 63.48, 27.40, 82.04 and 58,81 ng/L, respectively.

  4. Polycyclic Aromatic Hydrocarbon Ionization Energy Lowering in Water Ices

    Science.gov (United States)

    Gudipati, Murthy S.; Allamandola, Louis J.

    2004-01-01

    In studying various interstellar and solar system ice analogs, we have recently found that upon vacuum ultraviolet photolysis, polycyclic aromatic hydrocarbons (PAHs) frozen in water ice at low temperatures are easily ionized and indefinitely stabilized as trapped ions (Gudipati; Gudipati & Allamandola). Here we report the first experimental study that shows that PAH ionization energy is significantly lowered in PAH/H2O ices, in agreement with recent theoretical work (Woon & Park). The ionization energy (IE) of the PAH studied here, quaterrylene (C40H20, IE = 6.11 eV), is lowered by up to 2.11 eV in water ice. PAH ionization energy reduction in low-temperature water ice substantially expands the astronomical regions in which trapped ions and electrons may be important. This reduction in ionization energy should also hold for other types of trapped species in waterrich interstellar, circumstellar, and solar system ices. Subject headings: ISM: clouds - methods: laboratory - molecular processes - radiation mechanisms: nonthermal -ultraviolet: ISM - ultraviolet: solar system

  5. Polycyclic aromatic hydrocarbon formation under simulated coal seam pyrolysis conditions

    Institute of Scientific and Technical Information of China (English)

    Liu Shuqin; Wang Yuanyuan; Wang Caihong; Bao Pengcheng; Dang Jinli

    2011-01-01

    Coal seam pyrolysis occurs during coal seam fires and during underground coal gasification.This is an important source of polycyclic aromatic hydrocarbon (PAH) emission in China.Pyrolysis in a coal seam was simulated in a tubular furnace.The 16 US Environmental Protection Agency priority controlled PAHs were analyzed by HPLC.The effects of temperature,heating rate,pyrolysis atmosphere,and coal size were investigated.The results indicate that the 3-ring PAHs AcP and AcPy are the main species in the pyrolysis gas.The 2-ring NaP and the 4-ring Pyr are also of concern.Increasing temperature caused the total PAH yield to go through a minimum.The lowest value was obtained at the temperature of 600 ℃ Higher heating rates promote PAH formation,especially formation of the lower molecular weight PAHs.The typical heating rate in a coal seam,5 ℃/min,results in intermediate yields of PAHs.The total PAHs yield in an atmosphere of N2 is about 1.81 times that seen without added N2,which indicates that an air flow through the coal seam accelerates the formation of PAHs.An increase in coal particle size reduces the total PAHs emission but promotes the formation of 5- and 6-ring PAHs.

  6. Fibrous adsorbent for removal of aqueous aromatic hydrocarbons.

    Science.gov (United States)

    Jung, Yong-Jun; Kiso, Yoshiaki; Oguchi, Tatsuo; Yamada, Toshiro; Takagi, Hiroo; Nishimura, Kazuyuki

    2007-01-01

    Bundles of a strongly hydrophobic fibrous material (p-phenylene-2,6-benzobisoxazole; PBO; Zylon) were employed as an adsorbent for the removal of aqueous aromatic compounds, because the PBO fibers are too rigid to be woven and did not entrap suspended solids. The removal performance for nine kinds of polyaromatic hydrocarbons (PAHs) and di-(2-ethylhexyl) phthalate (DEHP) was evaluated. PAHs and DEHP at initial concentrations of 50 microg L(-1) were removed at 72.5-99.9% and ca. 95%, respectively, although the removal efficiencies were affected by the phase ratio (fiber weight/solution volume). The logarithm of the partition coefficient (log K) for planar PAHs was linearly correlated with the logarithm of the n-octanol/water partition coefficient (log P), but nonplanar PAHs, such as cis-stilbene, p-terphenyl, and o-terphenyl, showed significantly lower adsorption performance. The adsorbed PAHs were not desorbed effectively with CH3CN, CH2Cl2, and toluene. On the other hand, DEHP was effectively desorbed with methanol.

  7. Polycyclic aromatic hydrocarbons in household dust near diesel transport routes.

    Science.gov (United States)

    Kuo, Chung-Yih; Chen, Heng-Chun; Cheng, Fang-Ching; Huang, Li-Ru; Chien, Po-Shan; Wang, Jing-Ya

    2012-02-01

    A river-dredging project has been undertaken in Nantou, Taiwan. A large number of diesel vehicles carrying gravel and sand shuttle back and forth on the main roads. Ten stations along major thoroughfares were selected as the exposure sites for testing, while a small village located about 9 km from a main traffic route was selected as the control site. Levels of household dust loading at the exposure sites (60.3 mg/m(2)) were significantly higher than those at the control site (38.2 mg/m(2)). The loading (μg/m(2)) of t-PAHs (total polycyclic aromatic hydrocarbons) in the household dust at the exposure sites was significantly higher (P < 0.05) than was the case at the control site. The diagnostic ratios of PAHs showed that diesel emissions were the dominant source of PAHs at the exposure sites. The lack of a significant correlation between the concentrations of Fe and t-PAHs suggested that the t-PAHs in household dust might come from diverse sources. However, a significant correlation (P = 0.003) between the concentrations of Mo and t-PAHs implied that the most of the t-PAHs in the household dust might have resulted from diesel emissions. The lifetime cancer risks of BaP(eq) from household dust exposure were markedly higher than those resulting from inhalation exposure.

  8. Polycyclic aromatic hydrocarbons in Dalian soils: distribution and toxicity assessment

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Z.; Chen, J.W.; Yang, P.; Qiao, X.L.; Tian, F. [Dalian University of Technology, Dalian (China). Dept. of Environmental Science & Technology

    2007-07-01

    Concentrations of 15 polycyclic aromatic hydrocarbons (PAHs) were measured in surface soils collected from Dalian, China, for examination of distributions and composition profiles and their potential toxicity. The sum of 15 PAHs ({Sigma} PAHs) ranged from 190 to 8595 ng g{sup -1} dry weight, and showed an apparent urban-suburban-rural gradient in both {Sigma} PAHs and composition profiles. Using hierarchical cluster analysis (HCA), the sampling sites were grouped into four clusters corresponding to traffic area, park/residential area, suburban and rural areas. The ratios of naphthalene (Nap) and fluorene (Fl) versus fluoranthene (Flu), pyrene (Pyr) and indeno(1,2,3-cd) pyrene (InP) in the four clusters provided evidence of local distillation. The diagnostic ratios indicated the prevalent PAH sources were petroleum combustion and coal combustion in Dalian, and a cross plot of diagnostic ratios distinguished the urban samples from suburban and rural ones. Toxic potency assessment of soil PAHs presented a good relationship with benzo(a) pyrene (BaP) levels, toxic equivalent concentrations based on BaP (TEQ(BaP)) and dioxin-like toxic equivalent concentrations (TEQ(TCDD)). The study highlights that BaP is a good indicator for assessing the potential toxicity of PAHs, and presents a promising toxicity assessment method for soil PAHs.

  9. Polycyclic aromatic hydrocarbons and pesticides in soil of Vojvodina

    Directory of Open Access Journals (Sweden)

    Pucarević Mira M.

    2004-01-01

    Full Text Available The paper deals with several groups of compounds that represent the most frequent pollutants of soil in the world. The paper also reviews results of long-term studies conducted at the Institute of Field and Vegetable Crops in Novi Sad on the residues of pesticides and polycyclic aromatic hydrocarbons (PAHs in the soil of the Vojvodina Province. The analyzed samples have been found to contain residues of persistent pesticides and their metabolites lindane and its metabolites 6,20 μg/kg, alachlor 3,56 μg/kg, aldrin 2,3 μg/kg, heptachlor epoxide 0,99 μg/kg, chlordane 3,82 μg/kg, DDT and its metabolites 10,77 μg/kg, dieldrin 2,04 μg/kg, endrin 3,57 μg/kg and endrin aldehyde 1,36 μg/kg. Soil samples from Novi Sad municipality contained 53,69 μg/kg of DDT and its metabolites. The values of atrazine ranged from 0,0005 to 0,8 mg/kg. The values of PAHs were 6,64 mg/kg in industrial soil, 4,93 mg/kg in agricultural soil, and 4,55 mg/kg and 5,48 mg/kg in the Novi Sad municipality. The lowest value, 0.83 mg/kg, was found for nonagricultural/nonindustrial soils.

  10. Polycyclic aromatic hydrocarbons and pesticides in milk powder.

    Science.gov (United States)

    Dobrinas, Simona; Soceanu, Alina; Popescu, Viorica; Coatu, Valentina

    2016-05-01

    This Research Communication reports analysis of 37 compounds comprising polycyclic aromatic hydrocarbons (PAHs), organochlorine and organophosphate pesticides (OCPS and OPPS) in milk powder (one brand each of commercial infant formulae, follow-on formulae and baby formulae purchased from a local supermarket in Romania). The selected analytes were investigated using gas chromatography-mass spectrometry (GC-MS), gas chromatography with electron capture detector (GC-ECD) and gas chromatography with thermionic sensitive detection (GC-TSD). The estimated limits of detection for most target analytes were in the μg/kg level (range 0·001-0·320 µg/kg). The purpose of the study was to determine the selected analytes, to assess the exposure of babies and infants and to produce data for comparison with tolerable limits according to the European Union Regulations. In most of the samples the organochlorine pesticides values were under the limit of detection. Exceptions were heptachlor epoxide and endosulfan sulphate, the last of which was found in all analysed samples at low concentrations. We also found detectable levels of ethoprophos, parathion-methyl, chlorpyrifos, prothiofos, guthion, disulfoton and fenchlorphos in most of the analysed samples. Benzo[a]pyrene, which is used as an indicator for the presence of PAHs, was not detected in selected samples. The low level of exposure to contaminants indicates that there are no health risks for the infants and babies that consume this brand of milk powder formulae. PMID:27210498

  11. Some carcinogenic polycyclic aromatic hydrocarbons by photoacoustic spectroscopy

    Science.gov (United States)

    Garg, R. K.; Kumar, Pardeep; Ram, R. S.; Zaidi, Zahid H.

    1999-12-01

    Polycyclic aromatic hydrocarbons (PAHs) have attracted spectroscopists, astrophysicts and environmentalist because of their importance in our day to day life. It is well known that epoxides are produced during the metabolism of PAHs and have the requisite chemical reactivity to qualify them for the role as an ultimate carcinogenic form of PAHs. Several carcinogenic PAHs such as 3.4-benzopyrene, 1.2,3.4-dibenzopyrene, 3.4,9.10- dibenzopyrene etc. are found to be present in tobacco smoke and among air pollutants. Although PAH molecules are being studied for last several years by using conventional spectroscopy but no systematic attempt has been made to study non-radiative transitions. In our laboratory, we have studied many PAH molecules by a non-destructive technique with unique capability and sensitivity, known as Photoacoustic (PA) spectroscopy. PA spectroscopy is an analytical and research tool to get information about non-radiative transitions and singlet-triplet electronic transitions, where the conventional spectroscopic technique fails. The study of electronic transitions of some carcinogenic molecules are reported using PA and optical absorption spectra in boric acid glass in the region 250 - 400 nm. The electronic transitions of these molecules observed experimentally, have been interpreted using the optimized geometries and CNDO/S-CI method. A good agreement is found between the experimental and calculated results. Assignments of observed electronic transitions are made on the basis of singlet-triplet electronic transitions. Vibrations attached to these electronic transitions are attributed to the ground state vibrational modes.

  12. Fibrous adsorbent for removal of aqueous aromatic hydrocarbons.

    Science.gov (United States)

    Jung, Yong-Jun; Kiso, Yoshiaki; Oguchi, Tatsuo; Yamada, Toshiro; Takagi, Hiroo; Nishimura, Kazuyuki

    2007-01-01

    Bundles of a strongly hydrophobic fibrous material (p-phenylene-2,6-benzobisoxazole; PBO; Zylon) were employed as an adsorbent for the removal of aqueous aromatic compounds, because the PBO fibers are too rigid to be woven and did not entrap suspended solids. The removal performance for nine kinds of polyaromatic hydrocarbons (PAHs) and di-(2-ethylhexyl) phthalate (DEHP) was evaluated. PAHs and DEHP at initial concentrations of 50 microg L(-1) were removed at 72.5-99.9% and ca. 95%, respectively, although the removal efficiencies were affected by the phase ratio (fiber weight/solution volume). The logarithm of the partition coefficient (log K) for planar PAHs was linearly correlated with the logarithm of the n-octanol/water partition coefficient (log P), but nonplanar PAHs, such as cis-stilbene, p-terphenyl, and o-terphenyl, showed significantly lower adsorption performance. The adsorbed PAHs were not desorbed effectively with CH3CN, CH2Cl2, and toluene. On the other hand, DEHP was effectively desorbed with methanol. PMID:17585293

  13. Polycyclic aromatic hydrocarbons in Italian preserved food products in oil.

    Science.gov (United States)

    Sannino, Anna

    2016-06-01

    A method based on gas chromatography/ tandem mass spectrometry was used to assess levels of 16 EU priority polycyclic aromatic hydrocarbons (PAHs) in 48 preserved food products in oil including foods such as vegetables in oil, fish in oil and oil-based sauces obtained from the Italian market. The benzo[a]pyrene concentrations ranged from <0.04 to 0.40 µg kg(-1), and 72.9% of the samples showed detectable levels of this compound. The highest contamination level was observed for chrysene with three additional PAHs (benzo[a]anthracene, benzo[b]fluoranthene and benzo[c]fluorene) giving mean values higher than the mean value for benzo[a]pyrene. Chrysene was detected in all the samples at concentrations ranging from 0.07 to 1.80 µg kg(-1) (median 0.31 µg kg(-1)). The contamination expressed as PAH4 (sum of benzo(a)pyrene, chrysene, benzo(a)anthracene and benzo(b)fluoranthene), for which the maximum tolerable limit has been set by Commission Regulation (EU) No. 835/2011, varied between 0.10 and 2.94 µg kg(-1). PMID:26886159

  14. Polycyclic aromatic hydrocarbons (PAHs) removal by sorption: A review.

    Science.gov (United States)

    Lamichhane, Shanti; Bal Krishna, K C; Sarukkalige, Ranjan

    2016-04-01

    Polycyclic aromatic hydrocarbons (PAHs) are organic micro pollutants which are persistent compounds in the environment due to their hydrophobic nature. Concerns over their adverse effects in human health and environment have resulted in extensive studies on various types of PAHs removal methods. Sorption is one of the widely used methods as PAHs possess a great sorptive ability into the solid media and their low aqueous solubility property. Several adsorbent media such as activated carbon, biochar, modified clay minerals have been largely used to remove PAHs from aqueous solution and to immobilise PAHs in the contaminated soils. According to the past studies, very high removal efficiency could be achieved using the adsorbents such as removal efficiency of activated carbon, biochar and modified clay mineral were 100%, 98.6% and >99%, respectively. PAHs removal efficiency or adsorption/absorption capacity largely depends on several parameters such as particle size of the adsorbent, pH, temperature, solubility, salinity including the production process of adsorbents. Although many studies have been carried out to remove PAHs using the sorption process, the findings have not been consolidated which potentially hinder to get the correct information for future study and to design the sorption method to remove PAHs. Therefore, this paper summarized the adsorbent media which have been used to remove PAHs especially from aqueous solutions including the factor affecting the sorption process reported in 142 literature published between 1934 and 2015. PMID:26820781

  15. Fullerenes, fulleranes and polycyclic aromatic hydrocarbons in the Allende meteorite

    Science.gov (United States)

    Becker, L.; Bunch, T. E.

    1997-01-01

    In this paper, we confirm our earlier observations of fullerenes (C60 and C70) in the Allende meteorite (Becker et al., 1994a, 1995). Fullerene C60 was also detected in two separate C-rich (approximately 0.5-1.0%) dark inclusions (Heymann et al., 1987) that were hand picked from the Allende sample. The amounts of C60 detected were approximately 5 and approximately 10 ppb, respectively, which is considerably less than what was detected in the Allende 15/21 sample (approximately 100 ppb; Becker et al., 1994a, 1995). This suggests that fullerenes are heterogeneously distributed in the meteorite. In addition, we present evidence for fulleranes, (C60Hx), detected in separate samples by laser desorption (reflectron) time-of-flight (TOF) mass spectrometry (LDMS). The LDMS spectra for the Allende extracts were remarkably similar to the spectra generated for the synthetic fullerane mixtures. Several fullerane products were synthesized using a Rh catalyst (Becker et al., 1993a) and separated using high-performance liquid chromatography (HPLC). Polycyclic aromatic hydrocarbons (PAHs) were also observed ppm levels) that included benzofluoranthene and corannulene, a cup-shaped molecule that has been proposed as a precursor molecule to the formation of fullerenes in the gas phase (Pope et al., 1993).

  16. Anharmonicity and infrared bands of Polycyclic Aromatic Hydrocarbon (PAH) molecules

    Science.gov (United States)

    Petrignani, Annemieke; Maltseva, Elena; Candian, Alessandra; Mackie, Cameron; Huang, Xinchuan; Lee, Timothy J.; Tielens, Alexander; Oomens, Jos; Buma, Wybren Jan

    2015-08-01

    We present a systematic laboratory study of the CH stretching region in Polycyclic Aromatic Hydrocarbon (PAH) molecules of different shapes and sizes to investigate anharmonic behaviour and address the reliability of the never-validated but universally accepted scaling factors employed in astronomical PAH models. At the same time, new anharmonic theoretical quantum chemistry studies have been performed with the software program Spectro using our experimental data as benchmark. We performed mass and conformational-resolved, high-resolution spectroscopy of cold (~10K) linear and compact PAH molecules starting with naphthalene (C10H8) in the 3-µm CH stretching region. Surprisingly, the measured infrared spectra show many more strong modes than expected. Measurements of the deuterated counterparts demonstrate that these bands are the result of Fermi Resonances. First comparisons with harmonic and anharmonic DFT calculations using Gaussian 09 show that both approximations are not able to reproduce in detail the observed molecular reality. The improved anharmonic calculations performed with Spectro now include the effects of Fermi resonances and have been applied to PAHs for the first time. The analysis of the experimental data is greatly aided by these new theoretical quantum chemistry studies. Preliminary assignments are presented, aided by comparison between the observed rotational contour and the symmetry of candidate bands.

  17. Multiphoton ionization mass spectrometry of nitrated polycyclic aromatic hydrocarbons.

    Science.gov (United States)

    Tang, Yuanyuan; Imasaka, Tomoko; Yamamoto, Shigekazu; Imasaka, Totaro

    2015-08-01

    In order to suppress the fragmentation and improve the sensitivity for determination of nitrated polycyclic aromatic hydrocarbons (NPAHs), the mechanism of multiphoton ionization was studied for the following representative NPAHs, 9-nitroanthracene, 3-nitrofluoranthene, and 1-nitropyrene. The analytes were extracted from the PM2.5 on the sampling filter ultrasonically, and were measured using gas chromatography/multiphoton ionization/time-of-flight mass spectrometry with a femtosecond tunable laser in the range from 267 to 405 nm. As a result, a molecular ion was observed as the major ion and fragmentation was suppressed at wavelengths longer than 345 nm. Furthermore, the detection limit measured at 345 nm was measured to be the subpicogram level. The organic compounds were extracted from a 2.19 mg sample of particulate matter 2.5 (PM2.5), and the extract was subjected to multiphoton ionization mass spectrometry after gas chromatograph separation. The background signals were drastically suppressed at 345 nm, and the target NPAHs, including 9-nitroanthracene and 1-nitropyrene, were detected, and their concentrations were determined to be 5 and 3 pg/m(3), respectively. PMID:26048831

  18. Photoinduced toxicity of sediment-bound polycyclic aromatic hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Greenberg, B.M.; Duxbury, C.L.; Marwood, C.A.; Huang, X.D.; Dixon, D.G. [Univ. of Waterloo, Ontario (Canada)

    1994-12-31

    Polycyclic aromatic hydrocarbons (PAHs) are known to be both mutagenic and toxic. Light, in particular UV irradiation, increases their toxicity. Since aquatic plants cannot avoid PAHs or light, they are at risk. However, the major loadings of PAHs are in sediment. In this study the authors examined the assimilation of both intact and photomodified labelled PAHs bound to a surrogate, sediment (sand) by the higher aquatic plant Lemna gibba L. G-3. They found that simulated solar radiation significantly promoted the release of PAHs from sand and their assimilation by Lemna, although assimilation from the solid phase was slower than for chemicals placed directly into the aqueous medium. Toxicity of PAHs bound to sand was then measured by exposing plants to the sand-chemical composite for 8 d. Plants were exposed to both visible and SSR light conditions during this period, and toxicity was measured as inhibition of growth, inhibition of photosynthesis (chlorophyll fluorescence induction) and chlorosis. All three endpoints indicated that PAHs bound to a sediment phase can express phototoxicity and that the effects are most strongly promoted by the UV region of the solar spectrum. The authors have now extended this work to probe the effects of UV-B and PAHs on chloroplast development, with the finding that both stresses inhibit development of the photosynthetic apparatus.

  19. Separation and analysis of aromatic hydrocarbons from two Chinese coals

    Institute of Scientific and Technical Information of China (English)

    DING Ming-jie; LI Wen-dian; XIE Rui-lun; ZONG Ying; CAI Ke-ying; PENG Yao-li; ZONG Zhi-min; XIE Rui-lun; WEI Xian-yong

    2008-01-01

    Separation and analysis of aromatic hydrocarbons (AHs) from coals is of considerable significance for both fuel and non-fuel use of the coals. In present work two Chinese bituminous coals were selected for separation of AHs by ultrasonic extraction with CS2 followed by column chromatography using hexane as eluent. A series of AHs were separated from the two coals and analyzed by GC/MS. FTIR was employed to characterize the raw coals and the extracted residues. The results of GC/MS analysis show that the separated AHs are mono- to tetracyclic arenes, among which the principle AHs are alkyl naphthalenes and phenanthrenes. Obvious differences in the composition and the structure of AHs exist between the two coals, i.e., the AHs from Tongting coal tend to be higher rings compared to those from Pingshuo coal both from the variety and from the abundance of the AHs. FFIR analysis shows that the raw and extracted coals are similar in terms of functional groups, suggesting that the composition and structure of CS extract, especially the AHs, from coals can be used to interpret the coal structure to some extent.

  20. Eisenia fetida increased removal of polycyclic aromatic hydrocarbons from soil

    International Nuclear Information System (INIS)

    The removal of phenanthrene, anthracene and benzo(a)pyrene added at three different concentrations was investigated with or without earthworms (Eisenia fetida) within 11 weeks. Average anthracene removal by the autochthonous micro-organisms was 23%, 77% for phenanthrene and 13% for benzo(a)pyrene, while it was 51% for anthracene, 47% for benzo(a)pyrene and 100% for phenanthrene in soil with earthworms. At 50 and 100 mg phenanthrene kg-1 E. fetida survival was 91% and 83%, but at 150 mg kg-1 all died within 15 days. Survival of E. fetida in soil amended with anthracene ≤1000 mg kg-1 and benzo(a)pyrene ≤150 mg kg-1 was higher than 80% and without weight loss compared to the untreated soil. Only small amounts of PAHs were detected in the earthworms. It was concluded that E. fetida has the potential to remove large amounts of PAHs from soil, but more work is necessary to elucidate the mechanisms involved. - Addition of earthworms, Eisenia fetida, accelara removal of polycyclic aromatic hydrocarbons from soil

  1. Threshold Energies for Single Carbon Knockout from Polycyclic Aromatic Hydrocarbons

    CERN Document Server

    Stockett, M H; Chen, T; de Ruette, N; Giacomozzi, L; Wolf, M; Schmidt, H T; Zettergren, H; Cederquist, H

    2015-01-01

    We have measured absolute cross sections for ultrafast (fs) single-carbon knockout from Polycyclic Aromatic Hydrocarbon (PAH) cations as functions of He-PAH center-of-mass collision energy in the range 10-200 eV. Classical Molecular Dynamics (MD) simulations cover this range and extend up to 10$^5$ eV. The shapes of the knockout cross sections are well described by a simple analytical expression yielding experimental and MD threshold energies of $E_{th}^{Exp}=32.5\\pm 0.4$ eV and $E_{th}^{MD}=41.0\\pm 0.3$ eV, respectively. These are the first measurements of knockout threshold energies for molecules isolated \\emph{in vacuo}. We further deduce semi-empirical (SE) and MD displacement energies --- \\emph{i.e.} the energy transfers to the PAH molecules at the threshold energies for knockout --- of $T_{disp}^{SE}=23.3\\pm 0.3$ eV and $T_{disp}^{MD}=27.0\\pm 0.3$ eV. The semi-empirical results compare favorably with measured displacement energies for graphene $T_{disp}=23.6$ eV [Meyer \\emph{et al.} Phys. Rev Lett. \\tex...

  2. Investigation of polycyclic aromatic hydrocarbons from coal gasification

    Institute of Scientific and Technical Information of China (English)

    ZHOU Hong-cang; JIN Bao-sheng; ZHONG Zhao-ping; HUANG Ya-ji; XIAO Rui; LI Da-ji

    2005-01-01

    The hazardous organic pollutants generated from coal gasification, such as polycyclic aromatic hydrocarbons(PAHs), are highly mutagenic and carcinogenic. More researchers have paid particular attention to them. Using air and steam as gasification medium, the experiments of three kinds of coals were carried out in a bench-scale atmospheric fluidized bed gasifier. The contents of the 16 PAHs specified by US EPA in raw coal, slag, bag house coke, cyclone coke and gas were measured by HPLC to study the contents of PAHs in raw coal and the effects of the inherent characters of coals on the formation and release of PAHs in coal gasification. The experimental results showed that the distributions of PAHs in the gasified products are similar to raw coals and the total-PAHs content in coal gasification is higher than in raw coal(except Coal C). The total-PAHs contents increase and then decrease with the rise of fixed carbon and sulfur of coal while there has an opposite variation when volatile matters content increase. The quantities of PAHs reduce with the increase of ash content or the drop of heating value during coal gasification.

  3. Occupational exposure to Polycyclic Aromatic Hydrocarbons in wood dust

    Science.gov (United States)

    Huynh, C. K.; Schüpfer, P.; Boiteux, P.

    2009-02-01

    Sino-nasal cancer (SNC) represents approximately 3% of Oto-Rhino-Laryngology (ORL) cancers. Adenocarcinoma SNC is an acknowledged occupational disease affecting certain specialized workers such as joiners and cabinetmakers. The high proportion of woodworkers contracting a SNC, subjected to an estimated risk 50 to 100 times higher than that affecting the general population, has suggested various study paths to possible causes such as tannin in hardwood, formaldehyde in plywood and benzo(a)pyrene produced by wood when overheated by cutting tools. It is acknowledged that tannin does not cause cancer to workers exposed to tea dust. Apart from being an irritant, formaldehyde is also classified as carcinogenic. The path involving carcinogenic Polycyclic Aromatic Hydrocarbons (PAHs) emitted by overheated wood is attractive. In this study, we measured the particle size and PAHs content in dust emitted by the processing of wood in an experimental chamber, and in field situation. Quantification of 16 PAHs is carried out by capillary GC-ion trap Mass Spectrometric analysis (GC-MS). The materials tested are rough fir tree, oak, impregnated polyurethane (PU) oak. The wood dust contains carcinogenic PAHs at the level of μg.g-1 or ppm. During sanding operations, the PU varnish-impregnated wood produces 100 times more PAHs in dust than the unfinished wood.

  4. Occupational exposure to Polycyclic Aromatic Hydrocarbons in wood dust

    Energy Technology Data Exchange (ETDEWEB)

    Huynh, C K; Schuepfer, P; Boiteux, P, E-mail: chuynh@hospvd.c [Institute for Work and Health, rue du Bugnon 21, CH-1005 Lausanne (Switzerland)

    2009-02-01

    Sino-nasal cancer (SNC) represents approximately 3% of Oto-Rhino-Laryngology (ORL) cancers. Adenocarcinoma SNC is an acknowledged occupational disease affecting certain specialized workers such as joiners and cabinetmakers. The high proportion of woodworkers contracting a SNC, subjected to an estimated risk 50 to 100 times higher than that affecting the general population, has suggested various study paths to possible causes such as tannin in hardwood, formaldehyde in plywood and benzo(a)pyrene produced by wood when overheated by cutting tools. It is acknowledged that tannin does not cause cancer to workers exposed to tea dust. Apart from being an irritant, formaldehyde is also classified as carcinogenic. The path involving carcinogenic Polycyclic Aromatic Hydrocarbons (PAHs) emitted by overheated wood is attractive. In this study, we measured the particle size and PAHs content in dust emitted by the processing of wood in an experimental chamber, and in field situation. Quantification of 16 PAHs is carried out by capillary GC-ion trap Mass Spectrometric analysis (GC-MS). The materials tested are rough fir tree, oak, impregnated polyurethane (PU) oak. The wood dust contains carcinogenic PAHs at the level of mug.g{sup -1} or ppm. During sanding operations, the PU varnish-impregnated wood produces 100 times more PAHs in dust than the unfinished wood.

  5. Distribution of polycyclic aromatic hydrocarbons in lime spray dryer ash

    Energy Technology Data Exchange (ETDEWEB)

    Ping Sun; Panuwat Taerakul; Linda K. Weavers; Harold W. Walker [Ohio State University, Columbus, OH (United States). Department of Civil and Environmental Engineering and Geodetic Science

    2005-10-01

    Four lime spray dryer (LSD) ash samples were collected from a spreader stoker boiler and measured for their concentrations of 16 U.S. EPA specified polycyclic aromatic hydrocarbons (PAHs). Results showed that the total measured PAH concentration correlated with the organic carbon content of the LSD ash. Each LSD ash sample was then separated using a 140 mesh sieve into two fractions: a carbon-enriched fraction ({gt}140 mesh) and a lime-enriched fraction ({lt}140 mesh). Unburned carbon was further separated from the carbon-enriched fraction with a lithiumheteropolytungstate (LST) solution. PAH measurements on these different fractions showed that unburned carbon had the highest PAH concentrations followed by the carbon-enriched fraction, indicating that PAHs were primarily associated with the carbonaceous material in LSD ash. However, detectable levels of PAHs were also found in the lime-enriched fraction, suggesting that the fine spray of slaked lime may sorb PAH compounds from the flue gas in the LSD process. 37 refs., 5 figs., 4 tabs.

  6. Source and deposition of polycyclic aromatic hydrocarbons to Shanghai, China

    Institute of Scientific and Technical Information of China (English)

    Lili Yan; Xiang Li; Jianmin Chen; Xinjun Wang; Jianfei Du; Lin Ma

    2012-01-01

    Despite recent efforts to investigate the distribution and fate of polycyclic aromatic hydrocarbons (PAHs) in air,water,and soil,very little is known about their temporal change in wet deposition.As a result of increased attention to public health,a large-scale survey on the deposition flux and distribution of PAH contamination in rainwater was urgently conducted in Shanghai,China.In this study,163 rainwater samples were collected from six sites,and 15 PAH compounds were detected by the use of a simple solid phase microextraction (SPME) technique coupled with gas chromatography-mass spectrometry.The dominant PAH species monitored were naphthalene,phenanthrene,anthracene,and fluoranthene.The concentration of total PAHs per event was between 74 and 980 ng/L,with an average value of 481 ng/L,which is at the high end of worldwide figures.The annual deposition flux of PAHs in rainwater was estimated to be 4148 kg/yr in the Shanghai area,suggesting rainfall as a major possible pathway for removing PAHs from the atmosphere.Diagnostic analysis by the ratios of An/178 and F1/F1+Py suggested that combustion of grass,wood,and coal was the major contributor to PAHs in the Shanghai region.Back trajectory analysis also indicated that the pollutant sources could be from the southern part of China.

  7. Polycyclic aromatic hydrocarbon in urban soil from Beijing, China

    Institute of Scientific and Technical Information of China (English)

    LI Xing-hong; MA Ling-ling; LIU Xiu-fen; FU Shan; CHENG Hang-xin; XU Xiao-bai

    2006-01-01

    Polycyclic aromatic hydrocarbons (EPA-PAHs) in the urban surface soils from Beijing were determined using gas chromatography and mass spectrometry (GC-MS). It is significantly complementary for understanding the PAHs pollution in soil of integrated Beijing city on the basis of the information known in the outskirts. The total concentration of 16 EPA-PAH was from 0.467 to 5.470 μg/g and was described by the contour map. Compound profiles presented that the 4-, 5- and 6-ring PAHs were major compositions. The correlation analysis showed that PAHs have the similar source in the most sampling sites and BaP might be considered as the indicator of PAHs. Characteristic ratios of anthracene (An)/(An+ phenanthrene (Phe)), fluoranthene (Flu)/(Flu+pyrene (Pyr)) and benzo[a]pyrene (BaP)/benzo[g,h,i]perylene (BghiP) indicated that the PAHs pollutants probably mainly originated from the coal combustion and it was not negligible from vehicular emission. The level of PAHs in our study area was compared with other studies.

  8. Polycyclic aromatic hydrocarbons in Dalian soils: distribution and toxicity assessment.

    Science.gov (United States)

    Wang, Zhen; Chen, Jingwen; Yang, Ping; Qiao, Xianliang; Tian, Fulin

    2007-02-01

    Concentrations of 15 polycyclic aromatic hydrocarbons (PAHs) were measured in surface soils collected from Dalian, China, for examination of distributions and composition profiles and their potential toxicity. The sum of 15 PAHs (SigmaPAHs) ranged from 190 to 8595 ng g(-1) dry weight, and showed an apparent urban-suburban-rural gradient in both SigmaPAHs and composition profiles. Using hierarchical cluster analysis (HCA), the sampling sites were grouped into four clusters corresponding to traffic area, park/residential area, suburban and rural areas. The ratios of naphthalene (Nap) and fluorene (Fl) versus fluoranthene (Flu), pyrene (Pyr) and indeno(1,2,3-cd)pyrene (InP) in the four clusters provided evidence of local distillation. The diagnostic ratios indicated the prevalent PAH sources were petroleum combustion and coal combustion in Dalian, and a cross plot of diagnostic ratios distinguished the urban samples from suburban and rural ones. Toxic potency assessment of soil PAHs presented a good relationship with benzo(a)pyrene (BaP) levels, toxic equivalent concentrations based on BaP (TEQ(BaP)) and dioxin-like toxic equivalent concentrations (TEQ(TCDD)). The study highlights that BaP is a good indicator for assessing the potential toxicity of PAHs, and presents a promising toxicity assessment method for soil PAHs. PMID:17285163

  9. The hydrogen coverage of interstellar PAHs [Polycyclic Aromatic Hydrocarbons

    International Nuclear Information System (INIS)

    The rate at which the CH bond in interstellar Polycyclic Aromatic Hydrocarbons (PAHs) rupture due to the absorption of a uv photon has been calculated. The results show that small PAHs (less than or equal to 25 carbon atoms) are expected to be partially dehydrogenated in regions with intense uv fields, while large PAHs (greater than or equal to 25 atoms) are expected to be completely hydrogenated in those regions. Because estimate of the carbon content of interstellar PAHs lie in the range of 20 to 25 carbon atoms, dehydrogenation is probably not very important. Because of the absence of other emission features besides the 11.3 micrometer feature in ground-based 8 to 13 micrometer spectra, it has been suggested that interstellar PAHs are partially dehydrogenated. However, IRAS 8 to 22 micrometer spectra of most sources that show strong 7.7 and 11.2 micrometer emission features also show a plateau of emission extending from about 11.3 to 14 micrometer. Like the 11.3 micrometer feature, this new feature is attributed to the CH out of plane bending mode in PAHs. This new feature shows that interstellar PAHs are not as dehydrogenated as estimated from ground-based 8 to 13 micrometer spectra. It also constrains the molecular structure of interstellar PAHs. In particular, it seems that very condensed PAHs, such as coronene and circumcoronene, dominate the interstellar PAH mixture as expected from stability arguments

  10. Polycylcic Aromatic Hydrocarbons (PAH's) in dense cloud chemistry

    CERN Document Server

    Wakelam, Valentine

    2008-01-01

    Virtually all detailed gas-phase models of the chemistry of dense interstellar clouds exclude polycyclic aromatic hydrocarbons (PAH's). This omission is unfortunate because from the few studies that have been done on the subject, it is known that the inclusion of PAH's can affect the gas-phase chemistry strongly. We have added PAH's to our network to determine the role they play in the chemistry of cold dense cores. In the models presented here, we include radiative attachment to form PAH-, mutual neutralization between PAH anions and small positively-charged ions, and photodetachment. We also test the sensitivity of our results to changes in the size and abundance of the PAH's. Our results confirm that the inclusion of PAH's changes many of the calculated abundances of smaller species considerably. In TMC-1, the general agreement with observations is significantly improved contrary to L134N. This may indicate a difference in PAH properties between the two regions. With the inclusion of PAH's in dense cloud c...

  11. Polycyclic aromatic hydrocarbons in insular and coastal soils of the Russian Arctic

    Science.gov (United States)

    Abakumov, E. V.; Tomashunas, V. M.; Lodygin, E. D.; Gabov, D. N.; Sokolov, V. T.; Krylenkov, V. A.; Kirtsideli, I. Yu.

    2015-12-01

    The content and individual component compositions of polycyclic aromatic hydrocarbons in polar soils of the Russian Arctic sector have been studied. The contamination of soils near research stations is identified from the expansion of the range of individual polycyclic aromatic hydrocarbons, the abrupt increase in the content of heavy fractions, and the accumulation of benzo[ a]pyrene. Along with heavy hydrocarbons, light hydrocarbons (which are not only natural compounds, but also components of organic pollutants) are also accumulated in the contaminated soils. Heavy polycyclic aromatic hydrocarbons are usually of technogenic origin and can serve as markers of anthropogenic impact in such areas as Cape Sterligov, Cape Chelyuskin, and the Izvestii TsIK Islands. The content of benzo[ a]pyrene, the most hazardous organic toxicant, appreciably increases in soils around the stations, especially compared to the control; however, the level of MPC is exceeded only for the soils of Cape Chelyuskin.

  12. Enhanced dissipation of polycyclic aromatic hydrocarbons in the presence of fresh plant residues and their extracts

    International Nuclear Information System (INIS)

    The feasibility of using fresh plant residues and their extracts to stimulate the bio-dissipation of polycyclic aromatic hydrocarbons (PAHs) were highlighted. Wood chip, bamboo leave, orange peel and their water-extractable organic matter (WEOM) were chosen as amendment materials. Effect of WEOM on bio-dissipation (bioaccumulation and biodegradation) of phenanthrene and pyrene from water by two bacteria were investigated. Orange peel extract demonstrated the highest efficiency for stimulating PAHs removal by bacterium B1 (Pseudomonas putida), while bamboo leave extract was the best one to enhance PAHs bio-dissipation by bacterium B2 (unidentified bacterium isolated from PAHs-contaminated soil). Amended the actual contaminated soil with 1% plant residues, PAHs dissipation were increased by 15–20%, 20–39%, 14–24%, 12–23% and 17–26%, respectively, for 2-, 3-, 4-, 5- and 6-ring PAHs via stimulating indigenous microbial degradation activity. Bamboo leave exhibited the most effective one to stimulate dissipation of PAHs in contaminated soil. - Graphical abstract: Enhanced bio-dissipation of 15 PAHs in soil amended with fresh plant residues of wood chip (WC), orange peel (OP), and bamboo leave (BL). The individual symbol of AC, EC and BC is the abiotic sterile control, evaporation control and blank control. Highlights: ► The addition of fresh plant extracts significantly enhance PAHs bio-dissipation from water. ► Bioaccumulation and biodegradation contribute to the bio-dissipation of PAHs in solution. ► The added fresh plant residues promotes 15 PAHs dissipation in PAHs-contaminated soil. ► Stimulating indigenous microbial degradation activity contributes to PAHs dissipation. ► Bamboo leave exhibits the most effective one to stimulate dissipation of PAHs in soil. - It is feasible to amend fresh plant residues and their extracts to stimulate the bio-dissipation of polycyclic aromatic hydrocarbons in the contaminated environment.

  13. Magnetic graphene oxide as adsorbent for the determination of polycyclic aromatic hydrocarbon metabolites in human urine.

    Science.gov (United States)

    Zhu, Linli; Xu, Hui

    2014-09-01

    Detection of monohydroxy polycyclic aromatic hydrocarbons metabolites in urine is an advisable and valid method to assess human environmental exposure to polycyclic aromatic hydrocarbons. In this work, novel Fe3O4/graphene oxide composites were prepared and their application in the magnetic solid-phase extraction of monohydroxy polycyclic aromatic hydrocarbons in urine was investigated by coupling with liquid chromatography and mass spectrometry. In the hybrid material, superparamagnetic Fe3O4 nanoparticles provide fast separation to simplify the analytical process and graphene oxide provides a large functional surface for the adsorption. The prepared magnetic nanocomposites were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and vibrating sample magnetometry. The experimental conditions were optimized systematically. Under the optimal conditions, the recoveries of these compounds were in the range of 98.3-125.2%, the relative standard deviations ranged between 6.8 and 15.5%, and the limits of detection were in the range of 0.01-0.15 ng/mL. The simple, quick, and affordable method was successfully used in the analysis of human urinary monohydroxy polycyclic aromatic hydrocarbons in two different cities. The results indicated that the monohydroxy polycyclic aromatic hydrocarbons level in human urine can provide useful information for environmental exposure to polycyclic aromatic hydrocarbons.

  14. Putting corannulene in its place. Reactivity studies comparing corannulene with other aromatic hydrocarbons.

    Science.gov (United States)

    George, Stephen R D; Frith, Thomas D H; Thomas, Donald S; Harper, Jason B

    2015-09-14

    A series of aromatic hydrocarbons were investigated so as to compare the reactivity of corannulene with planar aromatic hydrocarbons. Corannulene was found to be more reactive than benzene, naphthalene and triphenylene to Friedel-Crafts acylation whilst electrophilic aromatic bromination was also used to confirm that triphenylene was less reactive than corannulene and that pyrene, perylene and acenaphthene were more so. The stabilisation of a neighbouring carbocation by the various aromatic systems was investigated through consideration of the rates of methanolysis of a series of benzylic alcohols. The reactivity series was found to parallel that observed for the electrophilic aromatic substitutions and both series are supported by computational studies. As such, a reactivity scale was devised that showed that corannulene was less reactive than would be expected for an aromatic planar species of similar pi electron count. PMID:26220565

  15. Quantitative determination of hydroxy polycylic aromatic hydrocarbons as a biomarker of exposure to carcinogenic polycyclic aromatic hydrocarbons.

    Science.gov (United States)

    Woudneh, Million B; Benskin, Jonathan P; Grace, Richard; Hamilton, M Coreen; Magee, Brian H; Hoeger, Glenn C; Forsberg, Norman D; Cosgrove, John R

    2016-07-01

    A high-resolution gas chromatography/high-resolution mass spectrometry (HRGC/HRMS) method was developed for quantitative analysis of hydroxy polycyclic aromatic hydrocarbons (OH-PAHs). Four hydroxy metabolites of known and suspected carcinogenic PAHs (benzo[a]pyrene (B[a]P), benz[a]anthracene (B[a]A), and chrysene (CRY)) were selected as suitable biomarkers of PAH exposure and associated risks to human health. The analytical method included enzymatic deconjugation, liquid - liquid extraction, followed by derivatization with methyl-N-(trimethylsilyl) trifluoroacetamide and instrumental analysis. Photo-induced oxidation of target analytes - which has plagued previously published methods - was controlled by a combination of minimizing exposure to light, employing an antioxidant (2-mercaptoethanol) and utilizing a nitrogen atmosphere. Stability investigations also indicated that conjugated forms of the analytes are more stable than the non-conjugated forms. Accuracy and precision of the method were 77.4-101% (<4.9% RSD) in synthetic urine and 92.3-117% (<15% RSD) in human urine, respectively. Method detection limits, determined using eight replicates of low-level spiked human urine, ranged from 13 to 24pg/mL. The method was successfully applied for analysis of a pooled human urine sample and 78 mouse urine samples collected from mice fed with PAH-contaminated diets. In mouse urine, greater than 94% of each analyte was present in its conjugated form. PMID:27266337

  16. Polycyclic Aromatic Hydrocarbons as Plausible Prebiotic Membrane Components

    OpenAIRE

    Groen, Joost; Deamer, David W.; Kros, Alexander; Ehrenfreund, Pascale

    2012-01-01

    Aromatic molecules delivered to the young Earth during the heavy bombardment phase in the early history of our solar system were likely to be among the most abundant and stable organic compounds available. The Aromatic World hypothesis suggests that aromatic molecules might function as container elements, energy transduction elements and templating genetic components for early life forms. To investigate the possible role of aromatic molecules as container elements, we incorporated different p...

  17. Aliphatic and aromatic hydrocarbons in Candiota coal samples: novel series of bicyclic compounds

    Energy Technology Data Exchange (ETDEWEB)

    Miranda, A.C.M.L.; Loureiro, M.R.B.; Cardoso, J.N. [Universidade Federal do Rio de Janeiro, Rio de Janeiro (Brazil). Inst. de Quimica

    1999-07-01

    Gas chromatography - mass spectrometry was used to analyse aliphatic and aromatic fractions obtained from nine samples taken from two different seams of five boreholes in the Candiota coalfield (Lower Permian). The occurrence of certain tetracyclic diterpenoids among the aliphatic hydrocarbons, and the tricyclic diterpenoids simonellite and retene in the aromatic hydrocarbon concentrates, suggest an important input from conifers to the sedimentary biomass. This may explain the origin of a novel series of saturated and aromatic bicyclic compounds detected in the extracts which may be structurally related to the same precursor, possibly a conifer resin-derived tricyclic diterpenoid.

  18. Biodegradation of polycyclic aromatic hydrocarbons by a bacterial consortium enriched from mangrove sediments.

    Science.gov (United States)

    Shahriari Moghadam, Mohsen; Ebrahimipour, Gholamhossein; Abtahi, Behrooz; Ghassempour, Alireza; Hashtroudi, Mehri Seyed

    2014-01-01

    Polycyclic aromatic hydrocarbons (PAHs) biodegradation in contaminated sediment is an attractive remediation technique and its success depends on the optimal condition for the PAH-degrading isolates. The aims of the current study was to isolate and identify PAHs-degrading bacteria from surface sediments of Nayband Bay and to evaluate the efficiency of statistically based experimental design for the optimization of phenanthrene (Phe) and Fluorene (Flu) biodegradation performed by enriched consortium. PAHs degrading bacteria were isolated from surface sediments. Purified strains were then identified by 16S rDNA gene sequence analysis. Taguchi L16 (4(5)) was employed to evaluate the optimum biodegradation of Phe and Flu by the enriched consortium. Total of six gram-negative bacterial strains including Marinobacter hydrocarbonoclasticus, Roseovarius pacificus, Pseudidiomarina sediminum and 3 unidentified strains were isolated from enrichment consortium, using Fluorene (Flu) and phenanthrene (Phe) as the sole carbon and energy source. The enriched consortium showed highest degradation abilities (64.0% Flu and 58.4% Phe degraded in 7 days) in comparison to a single strain cultures or mixtures. Maximum biodegradation efficiency was occur at temperature = 35°C; pH = 8; inoculum size = 0. 4 OD600nm; salinity = 40 ppt; C/N ratio = 100:10. In conclusion our results showed that, indigenous bacteria from mangrove surface sediments of Nayband Bay have high potential to degrade Flu and Phe with the best results achieved when enriched consortium was used. PMID:25436114

  19. Poly-3-hydroxybutyrate (PHB) production from alkylphenols, mono and poly-aromatic hydrocarbons using Bacillus sp. CYR1: A new strategy for wealth from waste

    OpenAIRE

    MOTAKATLA, Venkateswer Reddy; MAWATARI, Yasuteru; Yajima, Yuka; SEKI, Chigusa; Hoshino, Tamotsu; CHANG, Young-Cheol

    2015-01-01

    In the present study five different types of alkylphenols, each of the two different types of mono and poly-aromatic hydrocarbons were selected for degradation, and conversion into poly-3-hydroxybutyrate (PHB) using the Bacillus sp. CYR1. Strain CYR1 showed growth with various toxic organic compounds. Degradation pattern of all the organic compounds at 100 mg/l concentration with or without addition of tween-80 were analyzed using high pressure liquid chromatography (HPLC). Strain CYR1 showed...

  20. Near Infrared Spectra of Large Polycyclic Aromatic Hydrocarbons.

    Science.gov (United States)

    Mattioda, A. L.; Hudgins, D. M.; Bauschlicher, C. W.; Allamandola, L. J.

    The widespread, mid-IR interstellar emission features at 3.3, 6.2, 7.7, 8.6, and 11.2 microns are generally attributed to vibrationally excited polycyclic aromatic hydrocarbons (PAHs). Since these features typcially originate from radiation-rich regions, it has been generally thought that UV photons must dominate the interstellar excitation process since PAHs have very strong UV absorption bands. However, observations have shown that lower energy photons can also pump the emission (Aitken and Roche, Uchida and Sellgren), raising questions about the PAH model. Although it has long been known that larger PAHs should absorb at longer wavelengths (e.g. Schutte et. al., Salama et al., Li and Draine) data was not available for the isolated, neutral and ionized PAHs of sizes comparable to those thought responsible for the interstellar emission features. Here the matrix-isolated near-IR (NIR) spectra (from 0.7 to 2.5 microns) are presented for the anions and cations of PAHs ranging in size from C34H16 to C50H22. These molecules are characterized by strong absorption bands in this region, bands that can account for the emission of the interstellar features from UV poor regions. These NIR PAH transitions could also contribute to the extinction curve associated with the diffuse interstellar medium. For example, band overlap, as expected from a mixture of PAHs, can contribute to the continuum. Overlapping broad bands could lead to slight undulations in the continuum reminiscent of the Very Broad Structure (VBS, e.g. Hayes et al.). Furthermore, as previously pointed out, individual PAH bands may contribute to the diffuse interstellar band (DIB) spectrum (e.g. Romanini)

  1. Sorption characteristics of polycyclic aromatic hydrocarbons in aluminum smelter residues.

    Science.gov (United States)

    Breedveld, Gijs D; Pelletier, Emilien; St Louis, Richard; Cornelissen, Gerard

    2007-04-01

    High temperature carbon oxidation in primary aluminum smelters results in the release of polycyclic aromatic hydrocarbons (PAH) into the environment. The main source of PAH are the anodes, which are composed of petroleum coke (black carbon, BC) and coal tar pitch. To elucidate the dominant carbonaceous phase controlling the environmental fate of PAH in aluminum smelter residues (coke BC and/or coal tar), the sorptive behavior of PAHs has been determined, using passive samplers and infinitesink desorption methods. Samples directly from the wet scrubber were studied as well as ones from an adjacent 20-year old storage lagoon and roof dust from the smelter. Carbon-normalized distribution coefficients of native PAHs were 2 orders of magnitude higher than expected based on amorphous organic carbon (AOC)/water partitioning, which is in the same order of magnitude as reported literature values for soots and charcoals. Sorption isotherms of laboratory-spiked deuterated phenanthrene showed strong (-100 times stronger than AOC) but nonetheless linear sorption in both fresh and aged aluminum smelter residues. The absence of nonlinear behavior typical for adsorption to BC indicates that PAH sorption in aluminum smelter residues is dominated by absorption into the semi-solid coal tar pitch matrix. Desorption experiments using Tenax showed that fresh smelter residues had a relatively large rapidly desorbing fraction of PAH (35-50%), whereas this fraction was strongly reduced (11-16%) in the lagoon and roof dust material. Weathering of the coal tar residue and/or redistribution of PAH between coal tar and BC phases could explain the reduced availability in aged samples.

  2. Polycyclic aromatic hydrocarbons and heavy metals in Kostrena coastal area.

    Science.gov (United States)

    Linsak, Dijana Tomić; Linsak, Zeljko; Besić, Denis; Vojcić, Nina; Telezar, Mirna; Coklo, Miran; Susnić, Sasa; Mićović, Vladimir

    2011-12-01

    The aim of this study was to determine pollution by polycyclic aromatic hydrocarbons (PAH) and heavy metals in seawater and sediment in Kostrena coastal area, as well as their toxicity using bioluminescence based tests. Total PAH concentration in seawater ranged 1.7-155.3 ng/L. The share of carcinogenetic PAH was relatively high, ranging 22-48.3%. Nickel concentrations in seawater were beyond detection limits (chrome concentrations were beyond detection limits, and copper concentrations were also beyond detection limits or extremely low (up to 0.32 microg/L). EC50 values in seawater ranged 23.80-90.90 ng/L. Correlation between total PAH concentration and toxicity of seawater showed strong connection between them (r = 0.9579). Total PAH concentration in marine sediment ranged 58.02-1116 microg/kg dry weight (d.w.). The share of carcinogenetic PAH was extremely high ranging 10-53%. Nickel concentrations in marine sediment ranged 8-24 mg/kg d.w., vanadium concentrations ranged 24-42 mg/kg d.w., chrome concentrations ranged 11-19 mg/kg d.w., and copper concentrations ranged 7-25 mg/kg d.w. EC50 values in marine sediment ranged 818-4596 microg/kg d.w. Correlation between total PAH concentration and toxicity of marine sediment showed weak connection between them (r = 0.2590). Previous studies of seawater samples from areas of the Adriatic sea under the direct influence of oil industry did not include concentrations of heavy metals, which makes our study the first to present such comprehensive results. Our results point out the need for further evaluations and following of marine environment pollution and its consequences on living organisms and marine ecosystem in whole.

  3. POLYCYCLIC AROMATIC HYDROCARBONS AND THE DIFFUSE INTERSTELLAR BANDS: A SURVEY

    International Nuclear Information System (INIS)

    We discuss the proposal of relating the origin of some of the diffuse interstellar absorption bands (DIBs) to neutral polycyclic aromatic hydrocarbons (PAHs) present in translucent interstellar clouds. An assessment of ionized PAHs will be examined in a future report. The spectra of several cold, isolated gas-phase PAHs have been measured in the laboratory under experimental conditions that mimic the interstellar conditions and are compared with an extensive set of astronomical spectra of reddened, early-type stars. This comparison provides-for the first time-accurate upper limits for the abundances of specific PAH molecules along specific lines of sight, something not attainable from IR observations alone. The comparison of these unique laboratory data with high-resolution, high signal-to-noise ratio spectra leads to two major findings: (1) a finding specific to the individual molecules that were probed in this study and, which leads to the clear and unambiguous conclusion that the abundance of these specific neutral PAHs must be very low in the individual translucent interstellar clouds that were probed in this survey (PAH features remain below the level of detection) and, (2) a general finding that neutral PAHs exhibit intrinsic band profiles that are similar to the profile of the narrow DIBs indicating that the carriers of the narrow DIBs must have close molecular structure and characteristics. This study is the first quantitative survey of neutral PAHs in the optical range and it opens the way for unambiguous quantitative searches of PAHs in a variety of interstellar and circumstellar environments.

  4. Generation of polycyclic aromatic hydrocarbons (PAH during woodworking operations

    Directory of Open Access Journals (Sweden)

    Evin Danisman Bruschweiler

    2012-10-01

    Full Text Available Occupational exposures to wood dust have been associated with an elevated risk of sinonasal cancer (SNC. Wood dust is recognized as a human carcinogen but the specific cancer causative agent remains unknown. One possible explanation is a co-exposure to; wood dust and polycyclic aromatic hydrocarbons (PAHs. PAHs could be generated during incomplete combustion of wood due to heat created by use of power tools.To determine if PAHs are generated from wood during common woodworking operations, PAHs concentrations in wood dust samples collected in an experimental chamber operated under controlled conditions were analyzed. In addition, personal air samples from workers exposed to wood dust (n=30 were collected.Wood dust was generated using tree different power tools: vibrating sander, belt sander, and saw; and six wood materials: fir, Medium Density Fiberboard (MDF, beech, mahogany, oak and wood melamine. Monitoring of wood workers was carried out by means of personnel sampler device during wood working operations. We measured 21 PAHs concentrations in wood dust samples by capillary gas chromatographic-ion trap mass spectrometric analysis (GC-MS.Total PAH concentrations in wood dust varied greatly (0.24 – 7.95 ppm with the lowest being in MDF dust and the highest in wood melamine dust. Personal exposures to PAHs observed were between 37.5-119.8 ng m-3 among workers during wood working operations.Our results suggest that PAH exposures during woodworking operation are present and hence could play a role in the mechanism of cancer induction related to wood dust exposure.

  5. Heavy metal-immobilizing organoclay facilitates polycyclic aromatic hydrocarbon biodegradation in mixed-contaminated soil.

    Science.gov (United States)

    Biswas, Bhabananda; Sarkar, Binoy; Mandal, Asit; Naidu, Ravi

    2015-11-15

    Soils contaminated with a mixture of heavy metals and polycyclic aromatic hydrocarbons (PAHs) pose toxic metal stress to native PAH-degrading microorganisms. Adsorbents such as clay and modified clay minerals can bind the metal and reduce its toxicity to microorganisms. However, in a mixed-contaminated soil, an adsorption process more specific to the metals without affecting the bioavailability of PAHs is desired for effective degradation. Furthermore, the adsorbent should enhance the viability of PAH-degrading microorganisms. A metal-immobilizing organoclay (Arquad(®) 2HT-75-bentonite treated with palmitic acid) (MIOC) able to reduce metal (cadmium (Cd)) toxicity and enhance PAH (phenanthrene) biodegradation was developed and characterized in this study. The MIOC differed considerably from the parent clay in terms of its ability to reduce metal toxicity (MIOC>unmodified bentonite>Arquad-bentonite). The MIOC variably increased the microbial count (10-43%) as well as activities (respiration 3-44%; enzymatic activities up to 68%), and simultaneously maintained phenanthrene in bioavailable form in a Cd-phenanthrene mixed-contaminated soil over a 21-day incubation period. This study may lead to a new MIOC-assisted bioremediation technique for PAHs in mixed-contaminated soils.

  6. Polycyclic aromatic hydrocarbons storage by Fusarium solani in intracellular lipid vesicles

    Energy Technology Data Exchange (ETDEWEB)

    Verdin, Anthony [Laboratoire de Mycologie/Phytopathologie/Environnement, Universite du Littoral-Cote d' Opale, 17 avenue Bleriot, BP 699, 62228 Calais Cedex (France); Lounes-Hadj Sahraoui, Anissa [Laboratoire de Mycologie/Phytopathologie/Environnement, Universite du Littoral-Cote d' Opale, 17 avenue Bleriot, BP 699, 62228 Calais Cedex (France)]. E-mail: lounes@univ-littoral.fr; Newsam, Ray [Department of Biosciences, University of Kent, Canterbury CT2 7NJ (United Kingdom); Robinson, Gary [Department of Biosciences, University of Kent, Canterbury CT2 7NJ (United Kingdom); Durand, Roger [Laboratoire de Mycologie/Phytopathologie/Environnement, Universite du Littoral-Cote d' Opale, 17 avenue Bleriot, BP 699, 62228 Calais Cedex (France)

    2005-01-01

    Accumulation and elimination of polycyclic aromatic hydrocarbons (PAHs) were studied in the fungus Fusarium solani. When the fungus was grown on a synthetic medium containing benzo[a]pyrene, hyphae of F. solani contained numerous lipid vesicles which could be stained by the lipid-specific dyes: Sudan III and Rhodamine B. The fluorescence produced by Rhodamine B and PAH benzo[a]pyrene were at the same locations in the fungal hyphae, indicating that F. solani stored PAH in pre-existing lipid vesicles. A passive temperature-independent process is involved in the benzo[a]pyrene uptake and storage. Sodium azide, a cytochrome c oxidation inhibitor, and the two cytoskeleton inhibitors colchicine and cytochalasin did not prevent the transport and accumulation of PAH in lipid vesicles of F. solani hyphae. F. solani degraded a large range of PAHs at different rates. PAH intracellular storage in lipid vesicles was not necessarily accompanied by degradation and was common to numerous other fungi. - Fungi can store PAHs intracellularly in lipid vesicles independently of their PAH degradation abilities.

  7. Photodegradation of polycyclic aromatic hydrocarbons in soils under a climate change base scenario.

    Science.gov (United States)

    Marquès, Montse; Mari, Montse; Audí-Miró, Carme; Sierra, Jordi; Soler, Albert; Nadal, Martí; Domingo, José L

    2016-04-01

    The photodegradation of polycyclic aromatic hydrocarbons (PAHs) in two typical Mediterranean soils, either coarse- or fine-textured, was here investigated. Soil samples, spiked with the 16 US EPA priority PAHs, were incubated in a climate chamber at stable conditions of temperature (20 °C) and light (9.6 W m(-2)) for 28 days, simulating a climate change base scenario. PAH concentrations in soils were analyzed throughout the experiment, and correlated with data obtained by means of Microtox(®) ecotoxicity test. Photodegradation was found to be dependent on exposure time, molecular weight of each hydrocarbon, and soil texture. Fine-textured soil was able to enhance sorption, being PAHs more photodegraded than in coarse-textured soil. According to the EC50 values reported by Microtox(®), a higher detoxification was observed in fine-textured soil, being correlated with the outcomes of the analytical study. Significant photodegradation rates were detected for a number of PAHs, namely phenanthrene, anthracene, benzo(a)pyrene, and indeno(123-cd)pyrene. Benzo(a)pyrene, commonly used as an indicator for PAH pollution, was completely removed after 7 days of light exposure. In addition to the PAH chemical analysis and the ecotoxicity tests, a hydrogen isotope analysis of benzo(a)pyrene was also carried out. The degradation of this specific compound was associated to a high enrichment in (2)H, obtaining a maximum δ(2)H isotopic shift of +232‰. This strong isotopic effect observed in benzo(a)pyrene suggests that compound-specific isotope analysis (CSIA) may be a powerful tool to monitor in situ degradation of PAHs. Moreover, hydrogen isotopes of benzo(a)pyrene evidenced a degradation process of unknown origin occurring in the darkness.

  8. Photodegradation of polycyclic aromatic hydrocarbons in soils under a climate change base scenario.

    Science.gov (United States)

    Marquès, Montse; Mari, Montse; Audí-Miró, Carme; Sierra, Jordi; Soler, Albert; Nadal, Martí; Domingo, José L

    2016-04-01

    The photodegradation of polycyclic aromatic hydrocarbons (PAHs) in two typical Mediterranean soils, either coarse- or fine-textured, was here investigated. Soil samples, spiked with the 16 US EPA priority PAHs, were incubated in a climate chamber at stable conditions of temperature (20 °C) and light (9.6 W m(-2)) for 28 days, simulating a climate change base scenario. PAH concentrations in soils were analyzed throughout the experiment, and correlated with data obtained by means of Microtox(®) ecotoxicity test. Photodegradation was found to be dependent on exposure time, molecular weight of each hydrocarbon, and soil texture. Fine-textured soil was able to enhance sorption, being PAHs more photodegraded than in coarse-textured soil. According to the EC50 values reported by Microtox(®), a higher detoxification was observed in fine-textured soil, being correlated with the outcomes of the analytical study. Significant photodegradation rates were detected for a number of PAHs, namely phenanthrene, anthracene, benzo(a)pyrene, and indeno(123-cd)pyrene. Benzo(a)pyrene, commonly used as an indicator for PAH pollution, was completely removed after 7 days of light exposure. In addition to the PAH chemical analysis and the ecotoxicity tests, a hydrogen isotope analysis of benzo(a)pyrene was also carried out. The degradation of this specific compound was associated to a high enrichment in (2)H, obtaining a maximum δ(2)H isotopic shift of +232‰. This strong isotopic effect observed in benzo(a)pyrene suggests that compound-specific isotope analysis (CSIA) may be a powerful tool to monitor in situ degradation of PAHs. Moreover, hydrogen isotopes of benzo(a)pyrene evidenced a degradation process of unknown origin occurring in the darkness. PMID:26841292

  9. Polycyclic aromatic hydrocarbons (PAHs) biodegradation potential and diversity of microbial consortia enriched from tsunami sediments in Miyagi, Japan

    Energy Technology Data Exchange (ETDEWEB)

    Bacosa, Hernando Pactao, E-mail: hernando.bacosa@utexas.edu [Graduate School of Environmental Studies, Tohoku University, Aoba 6-6-20, Aramaki, Aoba-ku, Sendai 980-8579 (Japan); Marine Science Institute, The University of Texas at Austin, 750 Channel View Drive, Port Aransas, TX 78373 (United States); Inoue, Chihiro [Graduate School of Environmental Studies, Tohoku University, Aoba 6-6-20, Aramaki, Aoba-ku, Sendai 980-8579 (Japan)

    2015-02-11

    Highlights: • Most bacterial consortia from tsunami sediment degraded PAH mixture and pyrene. • The consortia were dominated by known and unknown PAHs-degrading bacteria. • Dokdonella clone is a potential new species and PAH degrader from tsunami sediment. • PAH-RHDα is better than nidA gene for estimating pyrene-degraders in the consortia. • First report on the PAH degradation and PAH-degrading bacteria from tsunami sediment. - Abstract: The Great East Japan Earthquake caused tsunamis and resulted in widespread damage to human life and infrastructure. The disaster also resulted in contamination of the environment by chemicals such as polycyclic aromatic hydrocarbons (PAHs). This study was conducted to investigate the degradation potential and describe the PAH-degrading microbial communities from tsunami sediments in Miyagi, Japan. PAH-degrading bacteria were cultured by enrichment using PAH mixture or pyrene alone as carbon and energy sources. Among the ten consortia tested for PAH mixture, seven completely degraded fluorene and more than 95% of phenanthrene in 10 days, while only four consortia partially degraded pyrene. Six consortia partially degraded pyrene as a single substrate. Polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE) revealed that each sample was dominated by unique microbial populations, regardless of sampling location. The consortia were dominated by known PAHs degraders including Sphingomonas, Pseudomonas, and Sphingobium; and previously unknown degraders such as Dokdonella and Luteimonas. A potentially novel and PAH-degrading Dokdonella was detected for the first time. PAH-ring hydroxylating dioxygenase (PAH-RHDα) gene was shown to be more effective than nidA in estimating pyrene-degrading bacteria in the enriched consortia. The consortia obtained in this study are potential candidates for remediation of PAHs contaminated soils.

  10. Polycyclic aromatic hydrocarbons (PAHs) biodegradation potential and diversity of microbial consortia enriched from tsunami sediments in Miyagi, Japan

    International Nuclear Information System (INIS)

    Highlights: • Most bacterial consortia from tsunami sediment degraded PAH mixture and pyrene. • The consortia were dominated by known and unknown PAHs-degrading bacteria. • Dokdonella clone is a potential new species and PAH degrader from tsunami sediment. • PAH-RHDα is better than nidA gene for estimating pyrene-degraders in the consortia. • First report on the PAH degradation and PAH-degrading bacteria from tsunami sediment. - Abstract: The Great East Japan Earthquake caused tsunamis and resulted in widespread damage to human life and infrastructure. The disaster also resulted in contamination of the environment by chemicals such as polycyclic aromatic hydrocarbons (PAHs). This study was conducted to investigate the degradation potential and describe the PAH-degrading microbial communities from tsunami sediments in Miyagi, Japan. PAH-degrading bacteria were cultured by enrichment using PAH mixture or pyrene alone as carbon and energy sources. Among the ten consortia tested for PAH mixture, seven completely degraded fluorene and more than 95% of phenanthrene in 10 days, while only four consortia partially degraded pyrene. Six consortia partially degraded pyrene as a single substrate. Polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE) revealed that each sample was dominated by unique microbial populations, regardless of sampling location. The consortia were dominated by known PAHs degraders including Sphingomonas, Pseudomonas, and Sphingobium; and previously unknown degraders such as Dokdonella and Luteimonas. A potentially novel and PAH-degrading Dokdonella was detected for the first time. PAH-ring hydroxylating dioxygenase (PAH-RHDα) gene was shown to be more effective than nidA in estimating pyrene-degrading bacteria in the enriched consortia. The consortia obtained in this study are potential candidates for remediation of PAHs contaminated soils

  11. Optimization and determination of polycyclic aromatic hydrocarbons in biochar-based fertilizers.

    Science.gov (United States)

    Chen, Ping; Zhou, Hui; Gan, Jay; Sun, Mingxing; Shang, Guofeng; Liu, Liang; Shen, Guoqing

    2015-03-01

    The agronomic benefit of biochar has attracted widespread attention to biochar-based fertilizers. However, the inevitable presence of polycyclic aromatic hydrocarbons in biochar is a matter of concern because of the health and ecological risks of these compounds. The strong adsorption of polycyclic aromatic hydrocarbons to biochar complicates their analysis and extraction from biochar-based fertilizers. In this study, we optimized and validated a method for determining the 16 priority polycyclic aromatic hydrocarbons in biochar-based fertilizers. Results showed that accelerated solvent extraction exhibited high extraction efficiency. Based on a Box-Behnken design with a triplicate central point, accelerated solvent extraction was used under the following optimal operational conditions: extraction temperature of 78°C, extraction time of 17 min, and two static cycles. The optimized method was validated by assessing the linearity of analysis, limit of detection, limit of quantification, recovery, and application to real samples. The results showed that the 16 polycyclic aromatic hydrocarbons exhibited good linearity, with a correlation coefficient of 0.996. The limits of detection varied between 0.001 (phenanthrene) and 0.021 mg/g (benzo[ghi]perylene), and the limits of quantification varied between 0.004 (phenanthrene) and 0.069 mg/g (benzo[ghi]perylene). The relative recoveries of the 16 polycyclic aromatic hydrocarbons were 70.26-102.99%.

  12. POLYCYCLIC AROMATIC HYDROCARBON CONTAMINATION LEVELS IN COLLECTED SAMPLES FROM VICINITY OF A HIGHWAY

    Directory of Open Access Journals (Sweden)

    S. V. Samimi ، R. Akbari Rad ، F. Ghanizadeh

    2009-01-01

    Full Text Available Tehran as the biggest city of Iran with a population of more than 10 millions has potentially high pollutant exposures of gas oil and gasoline combustion from vehicles that are commuting in the highways every day. The vehicle exhausts contain polycyclic aromatic hydrocarbons, which are produced by incomplete combustion and can be directly deposited in the environment. In the present study, the presence of polycyclic aromatic hydrocarbons contamination in the collected samples of a western highway in Tehran was investigated. The studied location was a busy highway in Tehran. High performance liquid chromatography equipped with florescence detector was used for determination of polycyclic aromatic hydrocarbons concentrations in the studied samples. Total concentration of the ten studied polycyclic aromatic hydrocarbons compounds ranged from 11107 to 24342 ng/g dry weight in the dust samples and increased from 164 to 2886 ng/g dry weight in the soil samples taken from 300 m and middle of the highway, respectively. Also the average of Σ PAHs was 1759 ng/L in the water samples of pools in parks near the highway. The obtained results indicated that polycyclic aromatic hydrocarbons contamination levels were very high in the vicinity of the highway.

  13. An Emission Inventory of Polycyclic Aromatic Hydrocarbons in China

    Science.gov (United States)

    Mu, Xilong; Zhu, Xianlei; Wang, Xuesong

    2015-04-01

    Polycyclic Aromatic Hydrocarbons (PAHs) are among the most dangerous compounds due to their high carcinogenic and mutagenic character. Emission inventory provides the primary data to account for the sources of ambient PAHs and server as a necessary database for effective PAHs pollution control. China is experiencing fast economic growth and large energy consumption, which might result in a large amount of PAHs anthropogenic emissions. Therefore, based on the previous studies and combined recently field emission measurements as well as socio-economic activity data, the development of a nationwide PAHs emission inventory is needed. In this work, the emission inventory of 16 PAHs listed as U.S. Environmental Protection Agency priority pollutants in China in the year 2012 is compiled. The emission amounts of PAHs were estimated as annual rates of emission-related activities multiplied by respective emission factors. The activities such as fuel consumption, including fossil fuel and biofuel, and socio-economic statistics were obtained from yearbook released by Chinese central government and/or provincial governments, as well as related industry reports. Emission factors were derived from the related literature. Recently reported emission factors from local measurements were used. The total emissions of PAHs were 120611 ton in 2012. In China, PAHs were emitted predominantly from domestic combustion of coal and biofuel, coking industry and motor vehicles, accounting for 72% of the total amount. PAHs emission profiles were significantly different between China and the other countries. The emission profile in China featured a relatively higher portion of high molecular weight species with carcinogenic potential due to large contributions of domestic combustion and coking industry. Domestic combustion of straw, coal and firewood emitted 19464 ton, 8831 ton, and 5062 ton of PAHs, respectively, which were much higher than those in other countries. Emission per capita showed

  14. The Origins of Polycyclic Aromatic Hydrocarbons: Are They Everywhere?

    Science.gov (United States)

    Allamandola, L. J.; Morrison, David (Technical Monitor)

    1994-01-01

    During the past 15 years considerable progress in observational techniques has been achieved in the middle-infrared region (5000-500 per centimeter, 2-20 micron), the region where most diagnostic molecular vibrations occur. Spectra of many different astronomical infrared sources, some deeply embedded in dark molecular clouds and others at their edges, are now available. These spectra provide a powerful probe, not only for the identification of interstellar molecules in both the gas and solid phases, but also of the physical and chemical conditions which prevail in these two very different domains. The two lectures will focus on the evidence that polycyclic aromatic hydrocarbons (PAHs) are an important, ubiquitous and abundant interstellar species. PAHs are. extremely stable species which can range in size from a few angstroms across to several hundred angstroms (PAHs are also the building blocks of amorphous carbon particles). This identification rests on the suggestive agreement between the laboratory spectra of PAHs with a set of IR emission bands which emanate from many different sources where ultraviolet starlight impinges on a "dusty" region. The picture is that individual PAHs are first pumped into highly vibrationally excited states and relax by fluorescence at their fundamental vibrational frequencies. That PAHs are a ubiquitous interstellar component has serious ramifications in other spectral regions as well, including the strong extinction in the ultraviolet, and the classic visible diffuse interstellar bands discovered more than 50 years ago (but unexplained to this day) The first part of the course will focus on the interpretation of astronomical spectra. The second lecture will start by showing how recent laboratory data on PAHs taken under realistic interstellar conditions has con borated the PAH hypothesis and led to great insight into the conditions in the PAH containing regions. This lecture will end by reviewing the ever-increasing evidence for

  15. Aromatic hydrocarbons in the atmospheric environment. Part III: personal monitoring

    Science.gov (United States)

    Ilgen, E.; Levsen, K.; Angerer, J.; Schneider, P.; Heinrich, J.; Wichmann, H.-E.

    As part of a larger study, personal sampling of the aromatic hydrocarbons benzene, toluene, ethylbenzene and the isomeric xylenes (BTEX) was carried out by 55 nonsmoking volunteers for a period of 14 days. Thirty-nine persons lived in a rural area near Hannover (Germany) with hardly any traffic at all, while 16 persons lived in a high-traffic city street in Hannover. The personal exposure level of the persons in the rural area (some commuting to Hannover) was: 2.9, 24.8, 2.4 and 7.7 μg m -3 for benzene, toluene, ethylbenzene and the sum of xylenes, respectively, while the corresponding data for the high traffic city streets were 4.0, 22.2, 2.8 and 9.7 μg m -3 (geometric means). Four microenvironments have been monitored which contribute to the total exposure to BTEX, i.e. the home, the outdoor air, the workplace and the car cabin. The most important microenvironment for non-working persons is the private home. The concentration of most BTEX in the private home is almost equal to the personal exposure level, demonstrating that the indoor pollution in the home makes by far the highest contribution to the total exposure. For working people (mostly office workers), the workplace is the second most important microenvironment contributing to the total BTEX exposure. Taking all working persons into consideration (independent of the location of their private home) the personal exposure level is higher by a factor of 1.2-1.4 than that of the workplace (for toluene this factor is 2.2). As already found by others, very high BTEX concentrations may be found in car cabins, in particular, if the engine is gasoline-driven. In the cabin of 44 cars in the rural/urban area average benzene concentrations (geometric mean) of 12/14 μg m -3 and a maximum value of ˜550 μg m -3 were found. On average, the participating volunteers drove their car for 45 min day -1 (i.e. 3% of the day). Nevertheless, the car cabin constitutes about 10% of the total benzene exposure. Refueling of the

  16. Emissions of polycyclic aromatic hydrocarbons from coking industries in China

    Institute of Scientific and Technical Information of China (English)

    Ling Mu; Lin Peng; Junji Cao; Qiusheng He; Fan Li; Jianqiang Zhang; Xiaofeng Liu

    2013-01-01

    This study set out to assess the characteristics of polycyclic aromatic hydrocarbon (PAH) emission from coking industries,with field samplings conducted at four typical coke plants.For each selected plant,stack flue gas samples were collected during processes that included charging coal into the ovens (CC),pushing coke (PC) and the combustion of coke-oven gas (CG).Sixteen individual PAHs on the US EPA priority list were analyzed by gas chromatography/mass spectrometry (GC/MS).Results showed that the total PAH concentrations in the flue gas ranged from 45.776 to 414.874 μg/m3,with the highest emission level for CC (359.545 μg/m3).The concentration of PAH emitted from the CC process in CP1 (stamp charging) was lower than that from CP3 and CP4 (top charging).Low-molecular-weight PAHs (i.e.,two-to three-ring PAHs) were predominant contributors to the total PAH contents,and Nap,AcPy,Flu,PhA,and AnT were found to be the most abundant ones.Total BaPeq concentrations for CC (2.248 iμg/m3) were higher than those for PC (1.838 μg/m3) and CG (1.082 μg/m3),and DbA was an important contributor to carcinogenic risk as BaP in emissions from coking processes.Particulate PAH accounted for more than 20% of the total BaPeq concentrations,which were significantly higher than the corresponding contributions to the total PAH mass concentration (5%).Both particulate and gaseous PAH should be taken into consideration when the potential toxicity risk of PAH pollution during coking processes is assessed.The mean total-PAH emission factors were 346.132 and 93.173 μg/kg for CC and PC,respectively.

  17. Polycyclic aromatic hydrocarbons in the South American environment.

    Science.gov (United States)

    Barra, Ricardo; Castillo, Caroline; Torres, Joao Paulo Machado

    2007-01-01

    Pollution of the environment with polycyclic aromatic hydrocarbons (PAHs) should be a global concern, especially in urbanized areas. In South American countries, where notable increase in urban populations has been observed in the past few years, reliable information about the pollution status of these urban environments is not always easily accessible, and therefore an effort to collect updated information is required. This review attempts to contribute by analyzing the existing information regarding environmental levels of PAHs in some South American countries. A regional trend for environmental PAH information is an uneven contribution, because some countries, such as Bolivia, Peru, Paraguay, and Ecuador, have reported no information at all in the scientific literature, reflecting to a certain extent the different patterns of economic, technical, and scientific development. PAH air monitoring is one of the areas that has received the most attention during the last few years, mainly in Brazil, Chile, and Argentina, where data represent a few geographical areas within the region. PAH levels in air from some urban areas in Argentina, Brazil, and Chile, considered moderate to high (100-1000ng/m3), are probably among the highest values reported in the open literature. Urbanization, vehicle pollution, and wood fires are the principal contributors to the high reported levels. In more temperate areas, a clear distinction is observed between summer and winter levels. PAH monitoring in soils is very limited within the region, with few data available, and most information indicates widespread pollution. In Brazil, values for many representative ecosystems were found. In Chile, data from forestry and agricultural areas indicate in general low concentrations, in spite of a relatively high detection frequency. Pollution levels in soils are highly dependent on their closeness to PAH sources and certain cultural practices (agricultural burnings, forest fires, etc.). Water PAH

  18. Polycyclic aromatic hydrocarbons in the South American environment.

    Science.gov (United States)

    Barra, Ricardo; Castillo, Caroline; Torres, Joao Paulo Machado

    2007-01-01

    Pollution of the environment with polycyclic aromatic hydrocarbons (PAHs) should be a global concern, especially in urbanized areas. In South American countries, where notable increase in urban populations has been observed in the past few years, reliable information about the pollution status of these urban environments is not always easily accessible, and therefore an effort to collect updated information is required. This review attempts to contribute by analyzing the existing information regarding environmental levels of PAHs in some South American countries. A regional trend for environmental PAH information is an uneven contribution, because some countries, such as Bolivia, Peru, Paraguay, and Ecuador, have reported no information at all in the scientific literature, reflecting to a certain extent the different patterns of economic, technical, and scientific development. PAH air monitoring is one of the areas that has received the most attention during the last few years, mainly in Brazil, Chile, and Argentina, where data represent a few geographical areas within the region. PAH levels in air from some urban areas in Argentina, Brazil, and Chile, considered moderate to high (100-1000ng/m3), are probably among the highest values reported in the open literature. Urbanization, vehicle pollution, and wood fires are the principal contributors to the high reported levels. In more temperate areas, a clear distinction is observed between summer and winter levels. PAH monitoring in soils is very limited within the region, with few data available, and most information indicates widespread pollution. In Brazil, values for many representative ecosystems were found. In Chile, data from forestry and agricultural areas indicate in general low concentrations, in spite of a relatively high detection frequency. Pollution levels in soils are highly dependent on their closeness to PAH sources and certain cultural practices (agricultural burnings, forest fires, etc.). Water PAH

  19. Occurrence and transformation of tricyclic aromatic hydrocarbons in low rank coals

    Energy Technology Data Exchange (ETDEWEB)

    Hazai, I.; Alexander, G. (Hungarian Academy of Sciences, Budapest (Hungary). Research Laboratory for Inorganic Chemistry)

    1991-08-01

    Aromatic components of extracts obtained from four low rank coal samples were investigated by gas chromatography-mass spectrometry. A number of compounds were observed for the first time. The tricyclic aromatic hydrocarbons were investigated in detail. They show close similarities in structure to those reported to be formed in laboratory dehydrogenation experiments. The co-occurrence of molecules in the same samples containing additional unsaturation as well as the aromatic ring(s), offers strong support for the hypothesis of progressive aromatization of diterpenoids. A hypothetical diagenetic pathway is proposed to explain the generation of many of the compounds present. In the pathway the following reactions were considered: aromatization (i.e. dehydrogenation), elimination of substituents, methyl shift, isomerization and side chain shortening of fully aromatized species. 40 refs., 5 figs., 2 tabs.

  20. Treatability assessment of polycyclic aromatic hydrocarbons contaminated marine sediments using permanganate, persulfate and Fenton oxidation processes.

    Science.gov (United States)

    Shih, Yu-Jen; Binh, Nguyen Thanh; Chen, Chiu-Wen; Chen, Chih-Feng; Dong, Cheng-Di

    2016-05-01

    Various chemical oxidation techniques, such as potassium permanganate (KMnO4), sodium persulfate (Na2S2O8), Fenton (H2O2/Fe(2+)), and the modified persulfate and Fenton reagents (activated by ferrous complexes), were carried out to treat marine sediments that were contaminated with polycyclic aromatic hydrocarbons (PAHs) and dredged from Kaohsiung Harbor in Taiwan. Experimental results revealed that KMnO4 was the most effective of the tested oxidants in PAH degradation. Owing to the high organic matter content in the sediment that reduced the efficiencies of Na2S2O8 and regular Fenton reactions, a large excess of oxidant was required. Nevertheless, KH2PO4, Na4P2O7 and four chelating agents (EDTA, sodium citrate, oxalic acid, and sodium oxalate) were utilized to stabilize Fe(II) in activating the Na2S2O8 and Fenton oxidations, while Fe(II)-citrate remarkably promoted the PAH degradation. Increasing the molecular weight and number of rings of PAH did not affect the overall removal efficiencies. The correlation between the effectiveness of the oxidation processes and the physicochemical properties of individual PAH was statistically analyzed. The data implied that the reactivity of PAH (electron affinity and ionization potential) affected its treatability more than did its hydrophobicity (Kow, Koc and Sw), particularly using experimental conditions under which PAHs could be effectively oxidized. PMID:26915591

  1. Bioremediation of polycyclic aromatic hydrocarbon-contaminated saline-alkaline soils of the former Lake Texcoco.

    Science.gov (United States)

    Betancur-Galvis, L A; Alvarez-Bernal, D; Ramos-Valdivia, A C; Dendooven, L

    2006-03-01

    Polycyclic aromatic hydrocarbons (PAHs) such as phenanthrene, anthracene and Benzo[a]pyrene (BaP) are toxic for the environment. Removing these components from soil is difficult as they are resistant to degradation and more so in soils with high pH and large salt concentrations as in soil of the former lake Texcoco, but stimulating soil micro-organisms growth by adding nutrients might accelerate soil restoration. Soil of Texcoco and an agricultural Acolman soil, which served as a control, were spiked with phenanthrene, anthracene and BaP, added with or without biosolid or inorganic fertilizer (N, P), and dynamics of PAHs, N and P were monitored in a 112-day incubation. Concentrations of phenanthrene did not change significantly in sterilized Acolman soil, but decreased 2-times in unsterilized soil and >25-times in soil amended with biosolid and NP. The concentration of phenanthrene in unsterilized soil of Texcoco was 1.3-times lower compared to the sterilized soil, 1.7-times in soil amended with NP and 2.9-times in soil amended with biosolid. In unsterilized Acolman soil, degradation of BaP was faster in soil amended with biosolid than in unamended soil and soil amended with NP. In unsterilized soil of Texcoco, degradation of BaP was similar in soil amended with biosolid and NP but faster than in the unamended soil. It was found that application of biosolid and NP increased degradation of phenanthrene, anthracene and BaP, but to a different degree in alkaline-saline soil of Texcoco compared to an agricultural Acolman soil.

  2. Microbial degradation of crude oil hydrocarbons on organoclay minerals.

    Science.gov (United States)

    Ugochukwu, Uzochukwu C; Manning, David A C; Fialips, Claire I

    2014-11-01

    The role of organoclays in hydrocarbon removal during biodegradation was investigated in aqueous clay/oil microcosm experiments with a hydrocarbon degrading microorganism community. The clays used for this study were Na-montmorillonite and saponite. These two clays were treated with didecyldimethylammonium bromide to produce organoclays which were used in this study. The study indicated that clays with high cation exchange capacity (CEC) such as Na-montmorillonite produced an organomontmorillonite that was inhibitory to biodegradation of the crude oil hydrocarbons. Extensive hydrophobic interaction between the organic phase of the organoclay and the crude oil hydrocarbons is suggested to render the hydrocarbons unavailable for biodegradation. However, untreated Na-montmorillonite was stimulatory to biodegradation of the hydrocarbons and is believed to have done so because of its high surface area for the accumulation of microbes and nutrients making it easy for the microbes to access the nutrients. This study indicates that unlike unmodified montmorillonites, organomontmorillonite may not serve any useful purpose in the bioremediation of crude oil spill sites where hydrocarbon removal by biodegradation is desired within a rapid time period. PMID:24956464

  3. Degradation of aromatic compounds and degradative pathway of 4-nitrocatechol by Ochrobactrum sp. B2.

    Science.gov (United States)

    Zhong, Qiuzan; Zhang, Haiyan; Bai, Wenqin; Li, Mei; Li, Baotong; Qiu, Xinghui

    2007-12-01

    The potential capacity of a soil methyl parathion-degrading bacterium strain, Ochrobactrum sp. B2, for degrading various aromatic compounds were investigated. The results showed B2 was capable of degrading diverse aromatic compounds, but amino-substituted benzene compounds, at a concentration up to 100 mg L(-1) in 4 days. B2 could use 4-nitrocatechol (4-NC) as a sole carbon and energy source with release of nitrite ion. The pathway for 4-NC degradation via 1,2,4-benzenetriol (BT) and hydroquinone (HQ) formation in B2 was proposed based on the identification and quantification of intermediates by gas chromatography-mass spectrometry (GC-MS), and high performance liquid chromatography (HPLC). Degradation studies carried out on a plasmid-cured derivative showed that the genes for 4-NC degradative pathway was plasmid-borne in B2, suggesting that B2 degrades both p-nitrophenol and 4-NC by enzymes encoded by genes on the same plasmid.

  4. Microbial degradation of monocyclic and polycyclic aromatic hydrocarbons in case of limited pollutant availability with nitrate as a potential electron acceptor; Der mikrobielle Abbau mono- und polyzyklischer aromatischer Kohlenwasserstoffe bei einer begrenzten Schadstoffverfuegbarkeit mit Nitrat als potentiellem Elektronenakzeptor

    Energy Technology Data Exchange (ETDEWEB)

    Linke, C.

    2001-07-01

    The possibility of using natural degradation processes for long-term remediation of tar oil contaminated sites was investigated. Field studies have shown that microbial decomposition of pollutants does take place in many sites but that it is limited by limited availability of pollutants and oxygen in soil. The investigations focused on the activation of BTEX and PAH degradation in situ by nitrate in the absence or in the presence of oxygen. Tensides should be used in order to enhance the availability of pollutants in water, especially in the case of hardly water-soluble PAH. A large-scale experiment was carried out on tar oil contaminated terrain; it was found that the availability of oxygen and not of PAH is the limiting factor so that adding of surfactants will not improve pollutant degradation. In contrast, the adding of tensides would mean even higher concentrations of oxygen-depleting substances in soil. [German] In der vorliegenden Arbeit wurden im Hinblick auf langfristige Sanierungsstrategien fuer teeroelkontaminierte Standorte Moeglichkeiten der Nutzung natuerlicher Abbauvorgaenge untersucht. Zahlreiche Feldstudien belegen, dass ein mikrobieller Schadstoffabbau an vielen Standorten stattfindet, dieser jedoch sowohl durch eine begrenzte Schadstoffverfuegbarkeit als auch durch den im Untergrund nur begrenzt zur Verfuegung stehenden Sauerstoff limitiert wird. Ziel dieser Arbeit war es abzuklaeren, inwiefern ein BTEX- und PAK-Abbau in situ auch in Abwesenheit von Sauerstoff durch Nitrat allein oder durch Nitrat in Kombination mit Sauerstoff aktiviert werden kann. Um insbesondere fuer die schlecht wasserloeslichen PAK eine ausreichende Schadstoffverfuegbarkeit zu gewaehrleisten, sollten auch Tenside zur Erhoehung der im Wasser vorliegenden Schadstoffmenge eingesetzt werden. Aufbauend auf die Laboruntersuchungen wurde im Rahmen von VEGAS{sup ix} ein Grossversuch zum mikrobiellen PAK-Abbau im Abstrom einer simulierten Teeroelkontamination durchgefuehrt

  5. Heavy metal-immobilizing organoclay facilitates polycyclic aromatic hydrocarbon biodegradation in mixed-contaminated soil

    Energy Technology Data Exchange (ETDEWEB)

    Biswas, Bhabananda; Sarkar, Binoy [Centre for Environmental Risk Assessment and Remediation, University of South Australia, Mawson Lakes Campus, SA 5095 (Australia); Cooperative Research Centre for Contamination Assessment and Remediation of the Environment, P.O. Box 486, Salisbury, SA 5106 (Australia); Mandal, Asit [Centre for Environmental Risk Assessment and Remediation, University of South Australia, Mawson Lakes Campus, SA 5095 (Australia); Division of Soil Biology, Indian Institute of Soil Science, Bhopal, Madhya Pradesh (India); Naidu, Ravi [Centre for Environmental Risk Assessment and Remediation, University of South Australia, Mawson Lakes Campus, SA 5095 (Australia); Cooperative Research Centre for Contamination Assessment and Remediation of the Environment, P.O. Box 486, Salisbury, SA 5106 (Australia)

    2015-11-15

    Highlights: • A novel metal-immobilizing organoclay (MIOC) synthesized and characterized. • MIOC immobilizes toxic metals and reduces metal bioavailability. • It enhances PAH-bioavailability to soil bacteria. • It improves microbial growth and activities in mixed-contaminated soils. • MIOC facilitates PAH-biodegradation in metal co-contaminated soils. - Abstract: Soils contaminated with a mixture of heavy metals and polycyclic aromatic hydrocarbons (PAHs) pose toxic metal stress to native PAH-degrading microorganisms. Adsorbents such as clay and modified clay minerals can bind the metal and reduce its toxicity to microorganisms. However, in a mixed-contaminated soil, an adsorption process more specific to the metals without affecting the bioavailability of PAHs is desired for effective degradation. Furthermore, the adsorbent should enhance the viability of PAH-degrading microorganisms. A metal-immobilizing organoclay (Arquad{sup ®} 2HT-75-bentonite treated with palmitic acid) (MIOC) able to reduce metal (cadmium (Cd)) toxicity and enhance PAH (phenanthrene) biodegradation was developed and characterized in this study. The MIOC differed considerably from the parent clay in terms of its ability to reduce metal toxicity (MIOC > unmodified bentonite > Arquad–bentonite). The MIOC variably increased the microbial count (10–43%) as well as activities (respiration 3–44%; enzymatic activities up to 68%), and simultaneously maintained phenanthrene in bioavailable form in a Cd-phenanthrene mixed-contaminated soil over a 21-day incubation period. This study may lead to a new MIOC-assisted bioremediation technique for PAHs in mixed-contaminated soils.

  6. Global fate and distribution of polycyclic aromatic hydrocarbons emitted from Europe and Russia

    Science.gov (United States)

    Sehili, Aissa M.; Lammel, Gerhard

    The long-range atmospheric transport (LRT) of polycyclic aromatic hydrocarbons (PAHs) is not fully understood and has hardly been addressed by model studies. By model experiments the LRT of PAH emissions into air from Europe and Russia is studied testing several scenarios of gas-particle partitioning and degradability by reaction with ozone and the hydroxyl and nitrate radicals for two PAHs, benzo[a]pyrene (BAP) and fluoranthene (FLT). The model used is the atmosphere general circulation model ECHAM5 with a dynamic modal aerosol sub-model, HAM, ozone and sulfur species chemistry and bidirectional mass exchange on 2D marine (ocean surface mixed layer) and terrestrial surfaces (top soil layer and vegetation surfaces). After 5 years the substances are found to be mostly distributed to the soil compartment (64-97% as the global mean, varying with substance and season), which after 10 years is still filling; 1-5% are found in air and 2-33% in ocean. It is found that the lifetime and vertical distribution of the substances in the atmosphere and the LRT potential are all significantly influenced by the partitioning and degradation scenario. The total environmental burden is higher when sorption to organic matter and black carbon are considered to determine gas-particle partitioning rather than adsorption to the surface of particulate matter. The effect is +20% for BAP but sevenfold for FLT. Concentrations in Arctic air are mostly underestimated by the model, which is partly explained by emissions not considered in the simulation. The comparison shows, however, that degradation of the sorbed BAP and FLT molecules should be significantly slower than the respective gaseous molecules and that absorptive partitioning is necessary to explain the LRT potential of FLT.

  7. Characterization of the contamination produced by uncontrolled dumping of aromatic hydrocarbons; Caracterizacion de la contaminacion producida por el vertido incontrolado de hidrocarburos aromaticos

    Energy Technology Data Exchange (ETDEWEB)

    Navarro Flores, A.; Collado Fernandez, D.

    1996-08-01

    Uncontrolled dumping of aromatic hydrocarbons (m, o and p-xylen, ethylbenzene, etc) in the Tenes Valley aquifer (Besos river bassin) has produced a very important contamination of alluvial aquifer, that shows high concentrations of m, p xylen (41 mg/l) in groundwater, at a very vulnerable area. site characterization shows high concentrations of Fe, Mn and Ba in groundwater, originated by degradation of organic pollutants. Numerical simulation of plume movement shows a conditioned mobilization contaminants by biodegradation process. (Author) 11 refs.

  8. Probing the role of polycyclic aromatic hydrocarbons in the photoelectric heating within photodissociation regions

    NARCIS (Netherlands)

    Okada, Y.; Pilleri, P.; Berne, O.; Ossenkopf, V.; Fuente, A.; Goicoechea, J. R.; Joblin, C.; Kramer, C.; Roellig, M.; Teyssier, D.; van der Tak, F. F. S.

    2013-01-01

    Aims. We observationally investigate the relation between the photoelectric heating efficiency in photodissociation regions (PDRs) and the charge of polycyclic aromatic hydrocarbons (PAHs), which are considered to play a key role in photoelectric heating. Methods. Using PACS onboard Herschel, we obs

  9. Novel β-cyclodextrin modified quantum dots as fluorescent probes for polycyclic aromatic hydrocarbons (PAHs)

    Institute of Scientific and Technical Information of China (English)

    Cui Ping Han; Hai Bing Li

    2008-01-01

    Water-soluble CdSe/ZnS quantum dots (QDs)were prepared via a simple sonochemical procedure using β-cyclodextrin (CD)as surface coating agent.The QDs displayed a sensitive emission enhancement for anthracene over other related polycyclic aromatic hydrocarbons,and the detection limit was around 1.6 × 10-8 mol/L.

  10. The NASA Ames Polycyclic Aromatic Hydrocarbon Infrared Spectroscopic Database : The Computed Spectra

    NARCIS (Netherlands)

    Bauschlicher, C. W.; Boersma, C.; Ricca, A.; Mattioda, A. L.; Cami, J.; Peeters, E.; de Armas, F. Sanchez; Saborido, G. Puerta; Hudgins, D. M.; Allamandola, L. J.

    2010-01-01

    The astronomical emission features, formerly known as the unidentified infrared bands, are now commonly ascribed to polycyclic aromatic hydrocarbons (PAHs). The laboratory experiments and computational modeling done at the NASA Ames Research Center to create a collection of PAH IR spectra relevant t

  11. 多环芳烃的加氢裂化%Hydrocracking of polycyclic aromatic hydrocarbons

    Institute of Scientific and Technical Information of China (English)

    张全信; 刘希尧

    2001-01-01

    This paper reviews the progress on the catalysts, reaction network and reaction mechanism for hydrocracking of polycyclic aromatic hydrocarbons in recent years.%本文综述了近年来多环芳烃加氢裂化反应催化剂、反应网络及反应机理等方面的研究进展。

  12. Weathering and toxicity of marine sediments contaminated with oils and polycyclic aromatic hydrocarbons

    NARCIS (Netherlands)

    Jonker, M.T.O.; Sinke, A.; Brils, J.M.; Murk, A.J.; Koelmans, A.A.

    2006-01-01

    Many sediments are contaminated with mixtures of oil residues and polycyclic aromatic hydrocarbons (PAHs), but little is known about the toxicity of such mixtures to sediment-dwelling organisms and the change in toxicity on weathering. In the present study, we investigated the effects of a seminatur

  13. Longitudinal study of excretion of metabolites of polycyclic aromatic hydrocarbons in urine from two psoriatic patients

    DEFF Research Database (Denmark)

    Hansen, Åse Marie; Poulsen, O M; Menné, T

    1993-01-01

    Coal tar, which is widely used in the treatment of patients with atopic dermatitis, chronic eczema, and psoriasis, contains a large amount of polycyclic aromatic hydrocarbons (PAH). Some of the PAH compounds are known either to be carcinogenic or to potentiate the effects of other carcinogenic...

  14. Gas-phase infrared spectra of cationized nitrogen-substituted polycyclic aromatic hydrocarbons

    NARCIS (Netherlands)

    Galué, Alvaro; Pirali, O.; Oomens, J.

    2010-01-01

    Gas-phase infrared spectra of several ionized nitrogen substituted polycyclic aromatic hydrocarbons (PANHs) have been recorded in the 600-1600 cm(-1) region via IR multiple-photon dissociation (IRMPD) spectroscopy. The UV photoionized PANH ions are trapped and isolated in a quadrupole ion trap where

  15. Gas-phase infrared spectra of cationized nitrogen-substituted polycyclic aromatic hydrocarbons

    NARCIS (Netherlands)

    H.A. Galué; O. Pirali; J. Oomens

    2010-01-01

    Gas-phase infrared spectra of several ionized nitrogen substituted polycyclic aromatic hydrocarbons (PANHs) have been recorded in the 600-1600 cm-1 region via IR multiple-photon dissociation (IRMPD) spectroscopy. The UV photoionized PANH ions are trapped and isolated in a quadrupole ion trap where t

  16. Availabiltiy and leaching of polycyclic aromatic hydrocarbons: Controlling processes and comparison of testing methods

    NARCIS (Netherlands)

    Roskam, G.; Comans, R.N.J.

    2009-01-01

    We have studied the availability and leaching of polycyclic aromatic hydrocarbons (PAHs) from two contaminated materials, a tar-containing asphalt granulate (¿16 US-EPA PAHs 3412 mg/kg) and gasworks soil (¿PAHs 900 mg/kg), by comparing results from three typical types of leaching tests: a column, se

  17. Extraction of polycyclic aromatic hydrocarbons from soot and sediment : solvent selection and implications for sorption mechanism

    NARCIS (Netherlands)

    Jonker, M.T.O.; Koelmans, A.A.

    2002-01-01

    Soot contains high levels of toxic compounds such as polycyclic aromatic hydrocarbons (PAHs). Extraction of PAHs from soot for quantitative analysis is difficult because the compounds are extremely tightly bound to the sorbent matrix. This study was designed to investigate the effect of solvent type

  18. Development of analytical methods for polycyclic aromatic hydrocarbons (PAHs) in airborne particulates:A review

    Institute of Scientific and Technical Information of China (English)

    LIU Li-bin; LIU Yan; LIN Jin-ming; TANG Ning; HAYAKAWA Kazuichi; MAEDA Tsuneaki

    2007-01-01

    In the present work,the different sample collection, pretreatment and analytical methods for polycyclic aromatic hydrocarbons (PAHs) in airborne particulates is systematacially reviewed, and the applications of these pretreatment and analytical methods for PAHs are compared in detail. Some comments on the future expectation are also presented.

  19. Polycyclic aromatic hydrocarbons and dust in regions of massive star formation

    NARCIS (Netherlands)

    Peeters, Els

    2002-01-01

    Polycyclic Aromatic Hydrocarbons (PAHs) are known on earth as a large family of tarry materials naturally present in for example coal and crude oil. In addition, they are also formed in the combustion of all sorts of carbonaceous fuels and hence are found in auto exhaust, cigarette smoke, candle soo

  20. Gas phase adiabatic electron affinities of cyclopenta-fused polycyclic aromatic hydrocarbons

    NARCIS (Netherlands)

    Todorov, P.D.; Koper, C.; van Lenthe, J.H.; Jenneskens, L.W.

    2008-01-01

    The B3LYP/DZP++ adiabatic electron affinity (AEA) of nine (non)-alternant polycyclic aromatic hydrocarbons are reported and discussed. Calculations became feasible for molecules this size by projecting out the near-linearly dependent part of the one-electron basis. Non-alternant PAH consisting of an

  1. Polycyclic aromatic hydrocarbon ionization as a tracer of gas flows through protoplanetary disk gaps

    NARCIS (Netherlands)

    K.M. Maaskant; M. Min; L.B.F.M. Waters; A.G.G.M. Tielens

    2014-01-01

    Context. Planet-forming disks of gas and dust around young stars contain polycyclic aromatic hydrocarbons (PAHs). Aims. We aim to characterize how the charge state of PAHs can be used as a probe of flows of gas through protoplanetary gaps. In this context, our goal is to understand the PAH spectra o

  2. Effect of three polycyclic aromatic hydrocarbons on nodulation of Rhizobium tropici CIAT 899 on Phaseolus vulgaris

    Energy Technology Data Exchange (ETDEWEB)

    Gonzalez-Paredes, Y.; Ferrera-Cerrato, R.; Alarcon, A.

    2009-07-01

    Polycyclic aromatic hydrocarbons (PAH) are ubiquitous organic pollutants that are considered toxic and carcinogenic compounds to living organisms. There us scarce information about the effect of PAH on symbiotic systems such as Azolla-Anabaena, arbuscular mycorrhizal fungi-plants, or legume-rhizobia. (Author)

  3. Supercooled liquid vapour pressures and related thermodynamic properties of polycyclic aromatic hydrocarbons determined by gas chromatography

    NARCIS (Netherlands)

    J.J.H. Haftka; J.R. Parsons; H.A.J. Govers

    2006-01-01

    A gas chromatographic method using Kovats retention indices has been applied to determine the liquid vapour pressure (P-i), enthalpy of vaporization (Delta H-i) and difference in heat capacity between gas and liquid phase (Delta C-i) for a group of polycyclic aromatic hydrocarbons (PAHs). This group

  4. COMPARATIVE STUDIES OF THE EFFECT OF POLYCYCLIC AROMATIC HYDROCARBON GEOMETRY ON THE HYDROLYSIS OF DIOL EPOXIDES

    Science.gov (United States)

    Comparative studies of the effect of polycyclic aromatic hydrocarbon geometry on the hydrolysis of diol epoxides The interaction of the diol epoxides (DEs) of both planar and non-planar PAHs with water have been examined using quantum mechanical and molecular dynamics. Th...

  5. [Retrieval of monocyclic aromatic hydrocarbons with differential optical absorption spectroscopy].

    Science.gov (United States)

    Xie, Pin-Hua; Fu, Qiang; Liu, Jian-Guo; Liu, Wen-Qing; Qin, Min; Li, Ang; Liu, Shi-Sheng; Wei, Qing-Nong

    2006-09-01

    Differential optical absorption spectroscopy (DOAS) technique has been used to measure trace gases in the atmosphere by their strongly structured absorption of radiation in the UV and visible spectral range, e. g. SO2, NO2, O3 etc. However, unlike the absorption spectra of SO2 and NO2, the analysis of aromatic compounds is difficult and strongly suffers from the cross interference of other absorbers (Herzberg bands of oxygen, ozone and sulfur dioxide), especially with relatively low concentrations of aromatic compounds in the atmosphere. In the present paper, the DOAS evaluation of aromatic compounds was performed by nonlinear least square fit with two interpolated oxygen optical density spectra at different path lengths and reference spectra of ozone at different temperature and SO2 cross section to correct the interference from absorbers of O2, O3 and SO2. The measurement of toluene, benzene, (m, p, o) xylene and phenol with a DOAS system showed that DOAS method is suitable for monocyclic aromatic compounds monitoring in the atmosphere. PMID:17112022

  6. Recalcitrance of polycyclic aromatic hydrocarbons in soil contributes to background pollution

    Energy Technology Data Exchange (ETDEWEB)

    Posada-Baquero, Rosa [Instituto de Recursos Naturales y Agrobiologia de Sevilla (IRNAS), C.S.I.C., Apartado 1052, E-41080 Seville (Spain); Ortega-Calvo, Jose-Julio, E-mail: jjortega@irnase.csic.es [Instituto de Recursos Naturales y Agrobiologia de Sevilla (IRNAS), C.S.I.C., Apartado 1052, E-41080 Seville (Spain)

    2011-12-15

    The microbial accessibility of native phenanthrene and pyrene was determined in soils representing background scenarios for pollution by polycyclic aromatic hydrocarbons (PAHs). The soils were selected to cover a wide range of concentrations of organic matter (1.7-10.0%) and total PAHs (85-952 {mu}g/kg). The experiments included radiorespirometry determinations of biodegradation with {sup 14}C-labeled phenanthrene and pyrene and chemical analyses to determine the residual concentrations of the native compounds. Part of the tests relied on the spontaneous biodegradation of the chemicals by native microorganisms; another part also involved inoculation with PAH-degrading bacteria. The results showed the recalcitrance of PAHs already present in the soils. Even after extensive mineralization of the added {sup 14}C-PAHs, the concentrations of native phenanthrene and pyrene did not significantly decrease. We suggest that aging processes operating at background concentrations may contribute to recalcitrance and, therefore, to ubiquitous pollution by PAHs in soils. - Highlights: > Background PAHs in soils are highly resistant to biodegradation. > Recalcitrance occurs even after inoculation with specialized microorganisms. > Recalcitrance is caused by a low bioaccessibility and aging. > Time (aging) seems a relevant factor causing recalcitrance. > Recalcitrance can explain ubiquitous PAH background pollution. - Background soil PAHs are highly resistant to biodegradation.

  7. Mycelia promote active transport and spatial dispersion of polycyclic aromatic hydrocarbons.

    Science.gov (United States)

    Furuno, Shoko; Foss, Susan; Wild, Ed; Jones, Kevin C; Semple, Kirk T; Harms, Hauke; Wick, Lukas Y

    2012-05-15

    To cope with heterogeneous subsurface environments mycelial microorganisms have developed a unique ramified growth form. By extending hyphae, they can obtain nutrients from remote places and transport them even through air gaps and in small pore spaces, repectively. To date, studies have been focusing on the role that networks play in the distribution of nutrients. Here, we investigated the role of mycelia for the translocation of nonessential substances, using polycyclic aromatic hydrocarbons (PAHs) as model compounds. We show that the hyphae of the mycelial soil oomycete Pythium ultimum function as active translocation vectors for a wide range of PAHs. Visualization by two-photon excitation microscopy (TPEM) demonstrated the uptake and accumulation of phenanthrene (PHE) in lipid vesicles and its active transport by cytoplasmic streaming of the hyphae ('hyphal pipelines'). In mycelial networks, contaminants were translocated over larger distances than by diffusion. Given their transport capacity and ubiquity, hyphae may substantially distribute remote hydrophobic contaminants in soil, thereby improving their bioavailability to bacterial degradation. Hyphal contaminant dispersal may provide an untapped potential for future bioremediation approaches. PMID:22559873

  8. Cancer risk assessments of Hong Kong soils contaminated by polycyclic aromatic hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Man, Yu Bon [School of Environmental and Resource Sciences, Zhejiang Agriculture and Forestry University, Lin’an, Zhejiang 311300 (China); State Key Laboratory in Marine Pollution - Croucher Institute for Environmental Sciences, Hong Kong Baptist University and City University of Hong Kong, Hong Kong SAR (China); Kang, Yuan [State Key Laboratory in Marine Pollution - Croucher Institute for Environmental Sciences, Hong Kong Baptist University and City University of Hong Kong, Hong Kong SAR (China); School of Chemistry and Environment, South China Normal University, Key Laboratory of Theoretical Chemistry of Environment, Ministry of Education, Higher Education Mega Center, Guangzhou 510006 (China); Wang, Hong Sheng [State Key Laboratory in Marine Pollution - Croucher Institute for Environmental Sciences, Hong Kong Baptist University and City University of Hong Kong, Hong Kong SAR (China); Department of Microbial and Biochemical Pharmacy, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006 (China); Lau, Winifred; Li, Hui; Sun, Xiao Lin [State Key Laboratory in Marine Pollution - Croucher Institute for Environmental Sciences, Hong Kong Baptist University and City University of Hong Kong, Hong Kong SAR (China); Giesy, John P. [Department of Biology and Chemistry and State Key Laboratory in Marine Pollution, City University of Hong Kong, Kowloon, Hong Kong, SAR (China); Chow, Ka Lai [State Key Laboratory in Marine Pollution - Croucher Institute for Environmental Sciences, Hong Kong Baptist University and City University of Hong Kong, Hong Kong SAR (China); Wong, Ming Hung, E-mail: mhwong@hkbu.edu.hk [School of Environmental and Resource Sciences, Zhejiang Agriculture and Forestry University, Lin’an, Zhejiang 311300 (China); State Key Laboratory in Marine Pollution - Croucher Institute for Environmental Sciences, Hong Kong Baptist University and City University of Hong Kong, Hong Kong SAR (China)

    2013-10-15

    Highlights: ► High levels of soil organic matter in soils render PAHs more resistant to degradation. ► Open burning site contain high concentrations of PAHs in Hong Kong. ► Car dismantling workshop can increase potential cancer risk on human. -- Abstract: The aim of this study was to evaluate soils from 12 different land use types on human cancer risks, with the main focus being on human cancer risks related to polycyclic aromatic hydrocarbons (PAHs). Fifty-five locations were selected to represent 12 different types of land use (electronic waste dismantling workshop (EW (DW)); open burning site (OBS); car dismantling workshop (CDW) etc.). The total concentrations of 16 PAHs in terms of total burden and their bioaccessibility were analysed using GC/MS. The PAHs concentrations were subsequently used to establish cancer risks in humans via three exposure pathways, namely, accident ingestion of soil, dermal contact soil and inhalation of soil particles. When the 95th centile values of total PAH concentrations were used to derive ingestion and dermal cancer risk probabilities on humans, the CDW land use type indicated a moderate potential for cancerous development (244 × 10{sup −6} and 209 × 10{sup −6}, respectively). Bioaccessible PAHs content in soil samples from CDW (3.60 × 10{sup −6}) were also classified as low cancer risk. CDW soil possessed a higher carcinogenic risk based on PAH concentrations. Bioremediation is recommended to treat the contaminated soil.

  9. Cancer risk assessments of Hong Kong soils contaminated by polycyclic aromatic hydrocarbons

    International Nuclear Information System (INIS)

    Highlights: ► High levels of soil organic matter in soils render PAHs more resistant to degradation. ► Open burning site contain high concentrations of PAHs in Hong Kong. ► Car dismantling workshop can increase potential cancer risk on human. -- Abstract: The aim of this study was to evaluate soils from 12 different land use types on human cancer risks, with the main focus being on human cancer risks related to polycyclic aromatic hydrocarbons (PAHs). Fifty-five locations were selected to represent 12 different types of land use (electronic waste dismantling workshop (EW (DW)); open burning site (OBS); car dismantling workshop (CDW) etc.). The total concentrations of 16 PAHs in terms of total burden and their bioaccessibility were analysed using GC/MS. The PAHs concentrations were subsequently used to establish cancer risks in humans via three exposure pathways, namely, accident ingestion of soil, dermal contact soil and inhalation of soil particles. When the 95th centile values of total PAH concentrations were used to derive ingestion and dermal cancer risk probabilities on humans, the CDW land use type indicated a moderate potential for cancerous development (244 × 10−6 and 209 × 10−6, respectively). Bioaccessible PAHs content in soil samples from CDW (3.60 × 10−6) were also classified as low cancer risk. CDW soil possessed a higher carcinogenic risk based on PAH concentrations. Bioremediation is recommended to treat the contaminated soil

  10. Removal of polycyclic aromatic hydrocarbons (PAHs) from inorganic clay mineral: Bentonite.

    Science.gov (United States)

    Karaca, Gizem; Baskaya, Hüseyin S; Tasdemir, Yücel

    2016-01-01

    There has been limited study of the removal of polycyclic aromatic hydrocarbons (PAHs) from inorganic clay minerals. Determining the amount of PAH removal is important in predicting their environmental fate. This study was carried out to the degradation and evaporation of PAHs from bentonite, which is an inorganic clay mineral. UV apparatus was designed specifically for the experiments. The impacts of temperature, UV, titanium dioxide (TiO2), and diethylamine (DEA) on PAH removal were determined. After 24 h, 75 and 44 % of ∑12 PAH in the bentonite were removed with and without UV rays, respectively. DEA was more effective as a photocatalyst than TiO2 during UV application. The ∑12 PAH removal ratio reached 88 % with the addition of DEA to the bentonite. It was concluded that PAHs were photodegraded at high ratios when the bentonite samples were exposed to UV radiation in the presence of a photocatalyst. At the end of all the PAH removal applications, higher evaporation ratios were obtained for 3-ring compounds than for heavier ones. More than 60 % of the amount of ∑12 PAH evaporated consisted of 3-ring compounds.

  11. Dissipation of polycyclic aromatic hydrocarbons (PAHs) in the rhizosphere: Synthesis through meta-analysis

    International Nuclear Information System (INIS)

    Polycyclic aromatic hydrocarbons (PAHs) are widespread and persistent organic pollutants with high carcinogenic effect and toxicity; their behavior and fate in the soil-plant system have been widely investigated. In the present paper, meta-analysis was used to explore the interaction between plant growth and dissipation of PAHs in soil based on the large body of published literature. Plants have a promoting effect on PAH dissipation in soils. There was no difference in PAH dissipation between soils contaminated with single and mixed PAHs. However, plants had a more obvious effect on PAH dissipation in freshly-spiked soils than in long-term field-polluted soils. Additionally, a positive effect of the number of microbial populations capable of degrading PAHs was observed in the rhizosphere compared with the bulk soil. Our meta-analysis established the importance of the rhizosphere effect on PAH dissipation in variety of the soil-plant systems. - The meta-analysis provides the first quantitative evidence of the positive effect of rhizosphere processes on PAH dissipation.

  12. Grating light reflection spectroelectrochemistry for detection of trace amounts of aromatic hydrocarbons in water

    Energy Technology Data Exchange (ETDEWEB)

    KELLY,MICHAEL J.; SWEATT,WILLIAM C.; KEMME,SHANALYN A.; KASUNIC,K.J.; BLAIR,DIANNA S.; ZAIDI,S.H.; MCNEIL,J.R.; BURGESS,L.W.; BRODSKY,A.M.; SMITH,S.A.

    2000-04-01

    Grating light reflection spectroscopy (GLRS) is an emerging technique for spectroscopic analysis and sensing. A transmission diffraction grating is placed in contact with the sample to be analyzed, and an incident light beam is directed onto the grating. At certain angles of incidence, some of the diffracted orders are transformed from traveling waves to evanescent waves. This occurs at a specific wavelength that is a function of the grating period and the complex index of refraction of the sample. The intensities of diffracted orders are also dependent on the sample's complex index of refraction. The authors describe the use of GLRS, in combination with electrochemical modulation of the grating, for the detection of trace amounts of aromatic hydrocarbons. The diffraction grating consisted of chromium lines on a fused silica substrate. The depth of the grating lines was 1 {micro}m, the grating period was 1 {micro}m, and the duty cycle was 50%. Since chromium was not suitable for electrochemical modulation of the analyte concentration, a 200 nm gold layer was deposited over the entire grating. This gold layer slightly degraded the transmission of the grating, but provided satisfactory optical transparency for the spectroelectrochemical experiments. The grating was configured as the working electrode in an electrochemical cell containing water plus trace amounts of the aromatic hydrocarbon analytes. The grating was then electrochemically modulated via cyclic voltammetry waveforms, and the normalized intensity of the zero order reflection was simultaneously measured. The authors discuss the lower limits of detection (LLD) for two analytes, 7-dimethylamino-1,2-benzophenoxazine (Meldola's Blue dye) and 2,4,6-trinitrotoluene (TNT), probed with an incident HeNe laser beam ({lambda} = 543.5 nm) at an incident angle of 52.5{degree}. The LLD for 7-dimethylamino-1,2-benzophenoxazine is approximately 50 parts per billion (ppb), while the LLD for TNT is approximately

  13. [Comparison of bioremediation of polycyclic aromatic hydrocarbons (PAHs) contaminated soil by composting in the spring and winter].

    Science.gov (United States)

    Fang, Yun; Zhao, Xiu-Lan; Wei, Yuan-Song; Yang, Yu; Shen, Ying; Zheng, Jia-Xi

    2010-06-01

    In this study, lab-scale bioremediation experiments of soil contaminated by polycyclic aromatic hydrocarbon (PAHs) with aerated composting were compared in the Spring and Winter. Results showed that PAHs degradation rate in the winter was higher than that in the spring, and the total PAHs degradation rates were over 70% for both Pile 1 (the dry weight ratio of soil, swine manure and sawdust as 1: 1: 1) and Pile 2 (the dry weight ratio of soil, swine manure and sawdust as 1: 3: 1), but the PAHs degradation rate of Pile 1 as 74.61% was higher than that of Pile 2 the degradation rates of low, middle, high benzene-ring types PAHs were 66.46%, 79.12%, 75.88%, respectively. After composting most of kinds of PAHs contents in soil were less than 1 000 microg/kg (dry weight) except BbF, for example, BbF contents of these two piles in the Spring, 25 000 microg/kg and 20 000 microg/kg, respectively, were much higher than those in the winter experiments, both less than 5 000 microg/kg. The first reaction order model was used to simulate degradation of PAHs during composting, and results showed that the model was fitted better in winter (R2 > 0.6) than in spring, and the half-life of PAHs degradation in winter was about 13 d.

  14. Non-covalent Interactions of Graphene with Polycyclic Aromatic Hydrocarbons

    NARCIS (Netherlands)

    Zygouri, Panagiota; Potsi, Georgia; Mouzourakis, Eleftherios; Spyrou, Konstantinos; Gournis, Dimitrios; Rudolf, Petra

    2015-01-01

    In this mini review we discuss the interactions of polyaromatic hydrocarbons (PAHs) with graphene and the experimental approaches developed so far to create novel graphene/PAH hybrids and composite systems. The utilization of these systems in electrical, biomedical and polymer-reinforcement applicat

  15. Adsorption of polar aromatic hydrocarbons on synthetic calcite

    DEFF Research Database (Denmark)

    Madsen, Lene; Grahl-Madsen, Laila; Grøn, Christian;

    1996-01-01

    The wettability of hydrocarbon reservoirs depends on how and to what extent the organic compounds are adsorbed onto the surfaces of calcite, quartz and clay. A model system of synthetic call cite, cyclohexane and the three probe molecules: benzoic acid, benzyl alcohol and benzylamine, have been...

  16. Polycyclic aromatic hydrocarbons in atmospheric depositions around the Venice Lagoon

    OpenAIRE

    Rossini, Paolo; Matteucci, Gabriele; Raccanelli, Stefano; Favotto, Maurizio; Guerzoni, Stefano; Gattolin, Massimo

    2007-01-01

    Studies have revealed the potential risks to which human health and ecosystems are exposed in the Venice Lagoon, due to the atmospheric deposition of persistent pollutants such as trace metals and organic compounds. A total of 77 atmospheric bulk deposition samples were collected monthly from April 2002 to December 2004, from three sites located in the cities of Mestre and Venice, and inside the industrial area of Porto Marghera. Samples were analyzed by HRGC/HRMS for polycyclic aromatic hydr...

  17. Biofilm and Planktonic Bacterial and Fungal Communities Transforming High-Molecular-Weight Polycyclic Aromatic Hydrocarbons.

    Science.gov (United States)

    Folwell, Benjamin D; McGenity, Terry J; Whitby, Corinne

    2016-04-15

    High-molecular-weight polycyclic aromatic hydrocarbons (HMW-PAHs) are natural components of fossil fuels that are carcinogenic and persistent in the environment, particularly in oil sands process-affected water (OSPW). Their hydrophobicity and tendency to adsorb to organic matter result in low bioavailability and high recalcitrance to degradation. Despite the importance of microbes for environmental remediation, little is known about those involved in HMW-PAH transformations. Here, we investigated the transformation of HMW-PAHs using samples of OSPW and compared the bacterial and fungal community compositions attached to hydrophobic filters and in suspension. It was anticipated that the hydrophobic filters with sorbed HMW-PAHs would select for microbes that specialize in adhesion. Over 33 days, more pyrene was removed (75% ± 11.7%) than the five-ring PAHs benzo[a]pyrene (44% ± 13.6%) and benzo[b]fluoranthene (41% ± 12.6%). For both bacteria and fungi, the addition of PAHs led to a shift in community composition, but thereafter the major factor determining the fungal community composition was whether it was in the planktonic phase or attached to filters. In contrast, the major determinant of the bacterial community composition was the nature of the PAH serving as the carbon source. The main bacteria enriched by HMW-PAHs werePseudomonas,Bacillus, andMicrobacteriumspecies. This report demonstrates that OSPW harbors microbial communities with the capacity to transform HMW-PAHs. Furthermore, the provision of suitable surfaces that encourage PAH sorption and microbial adhesion select for different fungal and bacterial species with the potential for HMW-PAH degradation. PMID:26850299

  18. Historical Distribution of Polycyclic Aromatic Hydrocarbons in Shallow Sediments from Lake Chapala, Mexico

    Science.gov (United States)

    Zárate-Del Valle, P. F.; Macías-Pérez, M. P.; Barajas-Martínez, C. D.; Gómez-Hermosillo, C. M.

    2008-12-01

    The incomplete combustion of fossil fuels and burning of vegetation and other organic materials release into the environment pollutants like polycyclic aromatic hydrocarbons (PAHs) which are ubiquitous pollutants. The environmental behavior of PAHs is characterized by very low solubility, high hydrophobic sorptive capacity (kow), low volatility and general chemical stability. These characteristics mean, in practice, that PAHs are environmentally persistent compounds that in aquatic systems, are strongly held to solid surfaces present as both suspended particles and bottom sediment. Additionally, because of their high partition to organic carbon, PAHs show a high rate of bioconcentration and an easy way to enter the food chain. A benthos type sediment core was collected (CHA-C: N20° 15.105'; W103° 03.104') from the depocenter of lake Chapala. The first 40 cm of the sedimentary column representing an ecological history of ~ 150 years (210Pb dating) were cutted every 2 cm (n=20). For each core sectioned, the presence of PAHs was evaluated by GC-MS following methods from the USEPA (EPA 3540C, EPA 3620C, EPA 8270C). For the first 30 cm deep only products resulting of PAHs degradation were identified, namely: Butilisobutilphtalate, 1,2-benzenedicarboxaldehyde, phenol and, cinnamaldehyde; we attibute the presence of these products to a faster transformation of PAHs by photo and metabolic degradation as well as to chemical oxydation. For the 30-40 cm deep, the presence of the follwing PAHs was detected: 1H-indene, 1,2- difluor-3,4,5-trimetylbenzenethylnaphthalene, naphthalene, anthracene, and phenantren. A study is in progress to determine the presence of PAHs in other sites of the lake. We conclude that shallow sediment (40 cm deep) from Lake Chapala could constitute a potentially large pool of PAHs.

  19. Novel Approach for Evaluating Secondary Organic Aerosol from Aromatic Hydrocarbons: Unified Method for Predicting Aerosol Composition and Formation.

    Science.gov (United States)

    Li, Lijie; Tang, Ping; Nakao, Shunsuke; Kacarab, Mary; Cocker, David R

    2016-06-21

    Innovative secondary organic aerosol (SOA) composition analysis methods normalizing aerosol yield and chemical composition on an aromatic ring basis are developed and utilized to explore aerosol formation from oxidation of aromatic hydrocarbons. SOA yield and chemical composition are revisited using 15 years of University of California, Riverside/CE-CERT environmental chamber data on 17 aromatic hydrocarbons with HC:NO ranging from 11.1 to 171 ppbC:ppb. SOA yield is redefined in this work by normalizing the molecular weight of all aromatic precursors to the molecular weight of the aromatic ring [Formula: see text], where i is the aromatic hydrocarbon precursor. The yield normalization process demonstrates that the amount of aromatic rings present is a more significant driver of aerosol formation than the vapor pressure of the precursor aromatic. Yield normalization also provided a basis to evaluate isomer impacts on SOA formation. Further, SOA elemental composition is explored relative to the aromatic ring rather than on a classical mole basis. Generally, four oxygens per aromatic ring are observed in SOA, regardless of the alkyl substitutes attached to the ring. Besides the observed SOA oxygen to ring ratio (O/R ∼ 4), a hydrogen to ring ratio (H/R) of 6 + 2n is observed, where n is the number of nonaromatic carbons. Normalization of yield and composition to the aromatic ring clearly demonstrates the greater significance of aromatic ring carbons compared with alkyl carbon substituents in determining SOA formation and composition. PMID:27177154

  20. Degradation of Total Petroleum Hydrocarbon in Phytoremediation Using Terrestrial Plants

    Directory of Open Access Journals (Sweden)

    Mushrifah Idris

    2014-06-01

    Full Text Available This study focused on the total petroleum hydrocarbon (TPH degradation in phytoremediation of spiked diesel in sand. The diesel was added to the sand that was planted with terrestrial plants. Four selected terrestrial plants used were Paspalum vaginatum Sw, Paspalums crobiculatum L. varbispicatum Hack, Eragrotis atrovirens (Desf. Trin. ex Steud and Cayratia trifolia (L. Domin since all the plants could survive at a hydrocarbon petroleum contaminated site in Malaysia. The samplings were carried out on Day 0, 7, 14, 28, 42 and 72. The analysis of the TPH was conducted by extracting the spiked sand using ultrasonic extraction. The determination of the TPH concentration in the sand was performed using GC-FID. The degradation of TPH depends on the plant species and time of exposure. The highest percentage degradation by P. vaginatum, P. scrobiculatum, E. atrovirens and C. trifolia were 91.9, 74.0, 68.9 and 62.9%, respectively. In conclusion, the ability to degrade TPH by plants were P. vaginatum > P. scrobiculatum > E. atrovirens> C. trifolia.

  1. Isolation of an extremely halophilic arhaeon Natrialba sp. C21 able to degrade aromatic compounds and to produce stable biosurfactant at high salinity.

    Science.gov (United States)

    Khemili-Talbi, Souad; Kebbouche-Gana, Salima; Akmoussi-Toumi, Siham; Angar, Yassmina; Gana, Mohamed Lamine

    2015-11-01

    Natrialba sp. strain C21 was isolated from oil contaminated saline water in Ain Salah (Algeria) and has exhibited a good potential for degrading phenol (3% v/v), naphthalene (3% v/v), and pyrene (3% v/v) at high salinity with high growth, enzymatic activity and biosurfactant production. Successful metabolism of aromatic hydrocarbon compounds of the strain Natrialba sp. C21 appears to require the ortho-cleavage pathway. Indeed, assays of the key enzymes involved in the ring cleavage of catechol 1, 2-dioxygenase indicated that degradation of the phenol, naphthalene and pyrene by strain Natrialba sp. C21 was via the ortho-cleavage pathway. Cells grown on aromatic hydrocarbons displayed greater ortho-activities mainly towards catechol, while the meta-activity was very low. Besides, biosurfactants derived from the strain C21 were capable of effectively emulsifying both aromatic and aliphatic hydrocarbons and seem to be particularly promising since they have particular adaptations like the increased stability at high temperature and salinity conditions. This study clearly demonstrates for the first time that strain belonging to the genera Natrialba is able to grow at 25% (w/v) NaCl, utilizing phenol, naphthalene, and pyrene as the sole carbon sources. The results suggest that the isolated halophilic archaeon could be a good candidate for the remediation process in extreme environments polluted by aromatic hydrocarbons. Moreover, the produced biosurfactant offers a multitude of interesting potential applications in various fields of biotechnology.

  2. Estrogenic Activity of Mineral Oil Aromatic Hydrocarbons Used in Printing Inks.

    Directory of Open Access Journals (Sweden)

    Patrick Tarnow

    Full Text Available The majority of printing inks are based on mineral oils (MOs which contain complex mixtures of saturated and aromatic hydrocarbons. Consumer exposure to these oils occurs either through direct skin contacts or, more frequently, as a result of MO migration into the contents of food packaging that was made from recycled newspaper. Despite this ubiquitous and frequent exposure little is known about the potential toxicological effects, particularly with regard to the aromatic MO fractions. From a toxicological point of view the huge amount of alkylated and unsubstituted compounds therein is reason for concern as they can harbor genotoxicants as well as potential endocrine disruptors. The aim of this study was to assess both the genotoxic and estrogenic potential of MOs used in printing inks. Mineral oils with various aromatic hydrocarbon contents were tested using a battery of in vitro assays selected to address various endpoints such as estrogen-dependent cell proliferation, activation of estrogen receptor α or transcriptional induction of estrogenic target genes. In addition, the comet assay has been applied to test for genotoxicity. Out of 15 MOs tested, 10 were found to potentially act as xenoestrogens. For most of the oils the effects were clearly triggered by constituents of the aromatic hydrocarbon fraction. From 5 oils tested in the comet assay, 2 showed slight genotoxicity. Altogether it appears that MOs used in printing inks are potential endocrine disruptors and should thus be assessed carefully to what extent they might contribute to the total estrogenic burden in humans.

  3. Fingerprints of polycyclic aromatic hydrocarbons (PAHs) in infrared absorption spectroscopy

    Science.gov (United States)

    Tommasini, Matteo; Lucotti, Andrea; Alfè, Michela; Ciajolo, Anna; Zerbi, Giuseppe

    2016-01-01

    We have analyzed a set of 51 PAHs whose structures have been hypothesized from mass spectrometry data collected on samples extracted from carbon particles of combustion origin. We have obtained relationships between infrared absorption signals in the fingerprint region (mid-IR) and the chemical structures of PAHs, thus proving the potential of IR spectroscopy for the characterization of the molecular structure of aromatic combustion products. The results obtained here for the spectroscopic characterization of PAHs can be also of interest in Materials Science and Astrophysics.

  4. Combination of biochar amendment and mycoremediation for polycyclic aromatic hydrocarbons immobilization and biodegradation in creosote-contaminated soil.

    Science.gov (United States)

    García-Delgado, Carlos; Alfaro-Barta, Irene; Eymar, Enrique

    2015-03-21

    Soils impregnated with creosote contain high concentrations of polycyclic aromatic hydrocarbons (PAH). To bioremediate these soils and avoid PAH spread, different bioremediation strategies were tested, based on natural attenuation, biochar application, wheat straw biostimulation, Pleurotus ostreatus mycoremediation, and the novel sequential application of biochar for 21 days and P. ostreatus 21 days more. Soil was sampled after 21 and 42 days after the remediation application. The efficiency and effectiveness of each remediation treatment were assessed according to PAH degradation and immobilization, fungal and bacterial development, soil eco-toxicity and legal considerations. Natural attenuation and biochar treatments did not achieve adequate PAH removal and soil eco-toxicity reduction. Biostimulation showed the highest bacterial development but low PAH degradation rate. Mycoremediation achieved the best PAH degradation rate and the lowest bioavailable fraction and soil eco-toxicity. This bioremediation strategy achieved PAH concentrations below Spanish legislation for contaminated soils (RD 9/2005). Sequential application of biochar and P. ostreatus was the second treatment most effective for PAH biodegradation and immobilization. However, the activity of P. ostreatus was increased by previous biochar application and PAH degradation efficiency was increased. Therefore, the combined strategy for PAH degradation have high potential to increase remediation efficiency.

  5. Combination of biochar amendment and mycoremediation for polycyclic aromatic hydrocarbons immobilization and biodegradation in creosote-contaminated soil.

    Science.gov (United States)

    García-Delgado, Carlos; Alfaro-Barta, Irene; Eymar, Enrique

    2015-03-21

    Soils impregnated with creosote contain high concentrations of polycyclic aromatic hydrocarbons (PAH). To bioremediate these soils and avoid PAH spread, different bioremediation strategies were tested, based on natural attenuation, biochar application, wheat straw biostimulation, Pleurotus ostreatus mycoremediation, and the novel sequential application of biochar for 21 days and P. ostreatus 21 days more. Soil was sampled after 21 and 42 days after the remediation application. The efficiency and effectiveness of each remediation treatment were assessed according to PAH degradation and immobilization, fungal and bacterial development, soil eco-toxicity and legal considerations. Natural attenuation and biochar treatments did not achieve adequate PAH removal and soil eco-toxicity reduction. Biostimulation showed the highest bacterial development but low PAH degradation rate. Mycoremediation achieved the best PAH degradation rate and the lowest bioavailable fraction and soil eco-toxicity. This bioremediation strategy achieved PAH concentrations below Spanish legislation for contaminated soils (RD 9/2005). Sequential application of biochar and P. ostreatus was the second treatment most effective for PAH biodegradation and immobilization. However, the activity of P. ostreatus was increased by previous biochar application and PAH degradation efficiency was increased. Therefore, the combined strategy for PAH degradation have high potential to increase remediation efficiency. PMID:25506817

  6. Enhanced degradation of mono aromatic hydrocarbons in sandy aquifer materials

    Energy Technology Data Exchange (ETDEWEB)

    Corseuil, Henry X. [Santa Catarina Univ., Florianopolis, SC (Brazil). Dept. de Engenharia Sanitaria; Weber Junior, W.J. [Michigan Univ., Ann Arbor, MI (United States). Dept. of Civil and Environmental Engineering

    1993-12-31

    The use of an inoculation technique to enhance rates of in-situ biodegradation of toxic organic contaminants by increasing subsurface populations of specific microorganisms is described. An external biologically active carbon (BAC) adsorber is demonstrated to be an efficient reactor system for collection, acclimation and enrichment of microorganisms for the inoculation process (author). 15 refs., 3 figs.

  7. Hydrocarbon degradation, plant colonization and gene expression of alkane degradation genes by endophytic Enterobacter ludwigii strains

    Energy Technology Data Exchange (ETDEWEB)

    Yousaf, Sohail [AIT Austrian Institute of Technology GmbH, Bioresources Unit, A-2444 Seibersdorf (Austria); Afzal, Muhammad [AIT Austrian Institute of Technology GmbH, Bioresources Unit, A-2444 Seibersdorf (Austria); National Institute for Biotechnology and Genetic Engineering (NIBGE), Faisalabad (Pakistan); Reichenauer, Thomas G. [AIT Austrian Institute of Technology GmbH, Environmental Resources and Technologies Unit, A-2444 Seibersdorf (Austria); Brady, Carrie L. [Forestry and Agricultural Biotechnology Institute, Department of Microbiology and Plant Pathology, University of Pretoria, Pretoria (South Africa); Sessitsch, Angela, E-mail: angela.sessitsch@ait.ac.at [AIT Austrian Institute of Technology GmbH, Bioresources Unit, A-2444 Seibersdorf (Austria)

    2011-10-15

    The genus Enterobacter comprises a range of beneficial plant-associated bacteria showing plant growth promotion. Enterobacter ludwigii belongs to the Enterobacter cloacae complex and has been reported to include human pathogens but also plant-associated strains with plant beneficial capacities. To assess the role of Enterobacter endophytes in hydrocarbon degradation, plant colonization, abundance and expression of CYP153 genes in different plant compartments, three plant species (Italian ryegrass, birdsfoot trefoil and alfalfa) were grown in sterile soil spiked with 1% diesel and inoculated with three endophytic E. ludwigii strains. Results showed that all strains were capable of hydrocarbon degradation and efficiently colonized the rhizosphere and plant interior. Two strains, ISI10-3 and BRI10-9, showed highest degradation rates of diesel fuel up to 68% and performed best in combination with Italian ryegrass and alfalfa. All strains expressed the CYP153 gene in all plant compartments, indicating an active role in degradation of diesel in association with plants. - Highlights: > E. ludwigii strains efficiently colonized plants in a non-sterile soil environment. > E. ludwigii strains efficiently expressed alkane degradation genes in plants. > E. ludwigii efficiently degraded alkane contaminations and promoted plant growth. > E. ludwigii interacted more effectively with Italian ryegrass than with other plants. > Degradation activity varied with plant and microbial genotype as well as with time. - Enterobacter ludwigii strains belonging to the E. cloacae complex are able to efficiently degrade alkanes when associated with plants and to promote plant growth.

  8. Proteomic characterization of plasmid pLA1 for biodegradation of polycyclic aromatic hydrocarbons in the marine bacterium, Novosphingobium pentaromativorans US6-1.

    Directory of Open Access Journals (Sweden)

    Sung Ho Yun

    Full Text Available Novosphingobium pentaromativorans US6-1 is a halophilic marine bacterium able to degrade polycyclic aromatic hydrocarbons (PAHs. Genome sequence analysis revealed that the large plasmid pLA1 present in N. pentaromativorans US6-1 consists of 199 ORFs and possess putative biodegradation genes that may be involved in PAH degradation. 1-DE/LC-MS/MS analysis of N. pentaromativorans US6-1 cultured in the presence of different PAHs and monocyclic aromatic hydrocarbons (MAHs identified approximately 1,000 and 1,400 proteins, respectively. Up-regulated biodegradation enzymes, including those belonging to pLA1, were quantitatively compared. Among the PAHs, phenanthrene induced the strongest up-regulation of extradiol cleavage pathway enzymes such as ring-hydroxylating dioxygenase, putative biphenyl-2,3-diol 1,2-dioxygenase, and catechol 2,3-dioxygenase in pLA1. These enzymes lead the initial step of the lower catabolic pathway of aromatic hydrocarbons through the extradiol cleavage pathway and participate in the attack of PAH ring cleavage, respectively. However, N. pentaromativorans US6-1 cultured with p-hydroxybenzoate induced activation of another extradiol cleavage pathway, the protocatechuate 4,5-dioxygenase pathway, that originated from chromosomal genes. These results suggest that N. pentaromativorans US6-1 utilizes two different extradiol pathways and plasmid pLA1 might play a key role in the biodegradation of PAH in N. pentaromativorans US6-1.

  9. Monitoring of polycyclic aromatic hydrocarbons in seafoods from Lake Timsah.

    Science.gov (United States)

    Mostafa, Gamal A

    2002-03-01

    Concentrations of polycyclic aromatic hydrpcarvons (PAHs) in some seafoods caught from Lake Timsah were determined. The tested samples were tilapia fish (Oreochromis aureus), crabs (Portuns pelagicus), bivalves (Venerupis decussata), clams (Strombus tricornis) and gastropods (Munes Sp.). Where these seafoods are locally and favorite consumed foods in the area around the lake (Ismailia governorate). Results showed that crabs contained significantly higher concentrations of both total and carcinogenic PAHs ranging from 1318.6 to 3767.4 and 1230.3 to 3442.2 microg kg(-1), respectively. Meanwhile, clams contained significantly lower levels with mean value of 28.4 microg kg(-1) for total and 24.4 microg kg(-1) for carcinogenic PAHs. The most frequently detected PAHs in the tested samples were indeno(1,2,3-cd)pyrene followed by benzo(a)pyrene, dibenzo(a,h)anthracene, and benzo(b)fluoranthene which are characterized as carcinogenic compounds. PMID:11970818

  10. Analysis of aliphatic and aromatic hydrocarbons in particulate matter in Madrid urban area

    International Nuclear Information System (INIS)

    Levels of n-alkanes and polycyclic aromatic hydrocarbons have been measured in the air particulate matter during six months, from January to June of 1987, in an urban area of Madrid. The hydrocarbons were collected on glass fiber filters by high volumen sampling. The extraction was carried out by Sohxlet and ultrasonic techniques. The extracts were clean-up on silicagel fractionation and the chromatographic analysis was performed by capillary column gas chromatographic. Final results are discussed as well as the immission values related to the possible emission sources. (Author)

  11. IUPAC-NIST Solubility Data Series. 101. Alcohols + Hydrocarbons + Water Part 3. C1-C3 Alcohols + Aromatic Hydrocarbons

    Science.gov (United States)

    Oracz, Paweł; Góral, Marian; Wiśniewska-Gocłowska, Barbara; Shaw, David G.; Mączyński, Andrzej

    2016-09-01

    The mutual solubilities and related liquid-liquid equilibria for 11 ternary systems of C1-C3 alcohols with aromatic hydrocarbons and water are exhaustively and critically reviewed. Reports of experimental determination of solubility that appeared in the primary literature prior to the end of 2012 are compiled. For nine systems, sufficient data are available (two or more independent determinations) to allow critical evaluation. All new data are expressed as mass percent and mole fraction as well as the originally reported units. In addition to the standard evaluation criteria used throughout the Solubility Data Series, an additional criterion was used for each of the evaluated systems. These systems include one binary miscibility gap in the hydrocarbon + water subsystem. The binary tie lines were compared with the recommended values published previously.

  12. Degradation Characteristics and Community Structure of a Hydrocarbon Degrading Bacterial Consortium

    Institute of Scientific and Technical Information of China (English)

    Li Zheng; Gu Guizhou; Zhao Chaocheng; Zhao Dongfeng

    2015-01-01

    A hydrocarbon degrading bacterial consortium KO5-2 was isolated from oil-contaminated soil of Karamay in Xinjiang, China, which could remove 56.9%of 10 g/L total petroleum hydrocarbons (TPH) at 30℃after 7 days of incu-bation, and could also remove 100%of lfuorene, 98.93%of phenanthrene and 65.73%of pyrene within 3, 7 and 9 days, respectively. Twelve strains from six different genera were isolated from KO5-2 and only eight ones were able to utilize the TPH. The denaturing gradient gel electrophoresis (DGGE) was used to investigate the microbial community shifts in ifve different carbon sources (including TPH, saturated hydrocarbons, lfuorene, phenanthrene and pyrene). The test results indi-cated that the community compositions of KO5-2 in carbon sources of TPH and saturated hydrocarbons, respectively, were roughly the same, while they were distinctive in the three different carbon sources of PAHs. Rhodococcus sp. and Pseudo-monas sp. could survive in the ifve kinds of carbon sources. Bacillus sp., Sphingomonas sp. and Ochrobactrum sp. likely played key roles in the degradation of saturated hydrocarbons, PAHs and phenanthrene, respectively. This study showed that speciifc bacterial phylotypes were associated with different contaminants and complex interactions between bacterial spe-cies, and the medium conditions inlfuenced the biodegradation capacity of the microbial communities involved in bioreme-diation processes.

  13. Polycyclic aromatic hydrocarbons affect survival and development of common snapping turtle (Chelydra serpentina) embryos and hatchlings

    Energy Technology Data Exchange (ETDEWEB)

    Van Meter, Robin J. [School of Environmental Science, Engineering, and Policy and Department of Bioscience and Biotechnology, Drexel University, 3141 Chestnut Street, Philadelphia, PA 19104 (United States)]. E-mail: robinjvanmeter@yahoo.com; Spotila, James R. [School of Environmental Science, Engineering, and Policy and Department of Bioscience and Biotechnology, Drexel University, 3141 Chestnut Street, Philadelphia, PA 19104 (United States)]. E-mail: spotiljr@drexel.edu; Avery, Harold W. [School of Environmental Science, Engineering, and Policy and Department of Bioscience and Biotechnology, Drexel University, 3141 Chestnut Street, Philadelphia, PA 19104 (United States)]. E-mail: Haltort@aol.com

    2006-08-15

    Polycyclic aromatic hydrocarbons (PAHs) are toxic compounds found in the John Heinz National Wildlife Refuge in Philadelphia, Pennsylvania. We assessed the impact of PAHs and crude oil on snapping turtle development and behavior by exposing snapping turtle eggs from the Refuge and from three clean reference sites to individual PAHs or a crude oil mixture at stage 9 of embryonic development. Exposure to PAHs had a significant effect on survival rates in embryos from one clean reference site, but not in embryos from the other sites. There was a positive linear relationship between level of exposure to PAHs and severity of deformities in embryos collected from two of the clean reference sites. Neither righting response nor upper temperature tolerance (critical thermal maximum, CTM) of snapping turtle hatchlings with no or minor deformities was significantly affected by exposure to PAHs. - Exposure to polycyclic aromatic hydrocarbons on the egg reduces survival of snapping turtle embryos and causes developmental abnormalities.

  14. Thyroid hormone binding proteins as novel targets for hydroxylated polyhalogenated aromatic hydrocarbons (PHAHs): possible implications for toxicity.

    NARCIS (Netherlands)

    Lans, M.C.

    1995-01-01

    Some toxic effects caused by polyhalogenated aromatic hydrocarbons (PHAHs) develop through alterations in the reproductive and thyroid hormone regulatory systems, thereby affecting (brain) development, reproduction and behaviour of several species (Stone, 1995, Birnbaum, 1994, for review: Brouwer et

  15. FORMATION OF POLYCYCLIC AROMATIC HYDROCARBONS AND THEIR GROWTH TO SOOT -A REVIEW OF CHEMICAL REACTION PATHWAYS. (R824970)

    Science.gov (United States)

    The generation by combustion processes of airborne species of current health concern such as polycyclic aromatic hydrocarbons (PAH) and soot particles necessitates a detailed understanding of chemical reaction pathways responsible for their formation. The present review discus...

  16. Hybrid pseudomonads engineered by two-step homologous recombination acquire novel degradation abilities toward aromatics and polychlorinated biphenyls

    Energy Technology Data Exchange (ETDEWEB)

    Suenaga, Hikaru [National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba (Japan). Bioproduction Research Inst.; Nonaka, Kazuhiko; Goto, Masatoshi [Kyushu Univ., Fukuoka (Japan). Dept. of Bioscience and Biotechnology; Fujihara, Hidehiko; Furukawa, Kensuke [Beppu Univ. (Japan). Dept. of Fermentation and Food Science

    2010-10-15

    Pseudomonas pseudoalcaligenes KF707 possesses a chromosomally encoded bph gene cluster responsible for the catabolism of biphenyl and polychlorinated biphenyls. Previously, we constructed chimeric versions of the bphA1 gene, which encodes a large subunit of biphenyl dioxygenase, by using DNA shuffling between bphA1 genes from P. pseudoalcaligenes KF707 and Burkholderia xenovorans LB400. In this study, we demonstrate replacement of the bphA1 gene with chimeric bphA1 sequence within the chromosomal bph gene cluster by two-step homologous recombination. Notably, some of the hybrid strains acquired enhanced and/or expanded degradation capabilities for specific aromatic compounds, including single aromatic hydrocarbons and polychlorinated biphenyls. (orig.)

  17. Genotoxicity in child populations exposed to Polycyclic Aromatic Hydrocarbons (PAHs) in the air from Tabasco, Mexico

    OpenAIRE

    Gamboa, Aldeco R.; Rodríguez T. Gamboa; Bravo, Alvarez H.; Wegman P. Ostrosky

    2008-01-01

    The economy of the state of Tabasco is based on oil extraction. However, this imposes major effects to the environment and communities. Examples are the Polycyclic Aromatic Hydrocarbons (PAHs) that may be found in the soil, water and sediment of the region. Their volatility makes them available to living beings and results in genotoxic activity. The purpose of this study was to quantify the levels of PAHs in the air at several points in the state, and to analyze their relationship with possib...

  18. Sexual maturation in relation to polychlorinated aromatic hydrocarbons: Sharpe and Skakkebaek's hypothesis revisited

    OpenAIRE

    Den Hond, Elly; Roels, Harry A.; Hoppenbrouwers, Karel; Nawrot, Tim; Thijs, Lutgarde; Vandermeulen, Corinne; Winneke, Gerhard; Vanderschueren, Dirk; Staessen, Jan A.

    2002-01-01

    Polychlorinated aromatic hydrocarbons (PCAHs) have been described as endocrine disruptors in animals and in accidentally or occupationally exposed humans. In the present study we examined the effect of moderate exposure to PCAHs on sexual maturation. Two hundred adolescents (mean age, 17.4 years) who resided in two polluted suburbs and a rural control area in Flanders (Belgium) participated. We measured the serum concentration of polychlorinated biphenyl (PCB) congeners 138, 153, and 180 and ...

  19. Molecular comparison of cultivable protozoa from a pristine and a polycyclic aromatic hydrocarbon polluted site

    OpenAIRE

    Lara, Enrique; Berney, Cédric; Ekelund, Flemming; Harms, Hauke; Chatzinotas, Antonis

    2010-01-01

    We compared the abundance and diversity of cultivable protozoa (flagellates and amoebae) in a polycyclic aromatic hydrocarbon (PAH) polluted soil and an unpolluted control, by isolating and cultivating clonal strains. The number of cultivable protozoa was higher in the polluted soil; however, the polluted soil displayed an impoverished community, dominated by certain taxa, such as Acanthamoeba sp. We isolated a total of 31 protozoan strains to characterize them morphologically and by 18S rRNA...

  20. Estimated IR and phosphorescence emission fluxes for specific Polycyclic Aromatic Hydrocarbons in the Red Rectangle

    CERN Document Server

    Mulas, G; Joblin, C; Toublanc, D

    2005-01-01

    Following the tentative identification of the blue luminescence in the Red Rectangle by Vijh et al. (2005), we compute absolute fluxes for the vibrational IR emission and phosphorescence bands of three small polycyclic aromatic hydrocarbons. The calculated IR spectra are compared with available ISO observations. A subset of the emission bands are predicted to be observable using presently available facilities, and can be used for an immediate, independent, discriminating test on their alleged presence in this well-known astronomical object.

  1. On-line DACC-HPLC analysis of polycyclic aromatic hydrocarbons in edible oils

    OpenAIRE

    Neđeral, Sandra; Pukec, Dragutin; Škevin, Dubravka; Kraljić, Klara; Obranović, Marko; Zrinjan, Petra

    2014-01-01

    In this work an HPLC method for determination of polycyclic aromatic hydrocarbons (PAH) in edible oils on a DACC (donor-acceptor complex chromatography) column coupled with an on-line HPLC system with fluorescent detection. Method was used to determine the content of individual PAHs in the refined sunflower oil, virgin olive oil, cold pressed pumpkin seed oil, dark sesame oil and pumpkin seed oil produced with roasting obtained from domestic market. Calibration and validation were conducted f...

  2. Determination of polycyclic aromatic hydrocarbons in water using an electrochemical DNA biosensor

    OpenAIRE

    R Manaffar; B Sehatnia; R Sabzi; Ehsani, A.

    2015-01-01

    Background and Objectives: Polycyclic aromatic hydrocarbons (PAHs) are widespread environmental contaminants in aquatic environments. These contaminants are generated through oil spills, manufactory processes, and industrial wastes or naturally through the incomplete combustion of coal, oil, gas, and wood waste. Most of these compounds are noted as carcinogenic and mutagenic. Therefore, detection of these pollutants by a sensitive and inexpensive method is very important. Materials and Method...

  3. Exposure to Polycyclic Aromatic Hydrocarbons, Plasma Cytokines, and Heart Rate Variability

    OpenAIRE

    Binyao Yang; Qifei Deng; Wangzhen Zhang; Yingying Feng; Xiayun Dai; Wei Feng; Xiaosheng He; Suli Huang; Xiao Zhang; Xiaohai Li; Dafeng Lin; Meian He; Huan Guo; Huizhen Sun; Jing Yuan

    2016-01-01

    Epidemiological studies have suggested associations between polycyclic aromatic hydrocarbons (PAHs) and heart rate variability (HRV). However, the roles of plasma cytokines in these associations are limited. In discovery stage of this study, we used Human Cytokine Antibody Arrays to examine differences in the concentrations of 280 plasma cytokines between 8 coke-oven workers and 16 community residents. We identified 19 cytokines with significant different expression (fold change ≥2 or ≤−2, an...

  4. Estimation of individual dermal and respiratory uptake of polycyclic aromatic hydrocarbons in 12 coke oven workers.

    OpenAIRE

    VanRooij, J G; Bodelier-Bade, M M; Jongeneelen, F.J.

    1993-01-01

    Twelve workers from a coke plant in The Netherlands participated in an intensive skin monitoring programme combined with personal air sampling and biological monitoring during five consecutive eight hour workshifts. The purpose of the study was to make a quantitative assessment of both the dermal and respiratory intake of polycyclic aromatic hydrocarbons (PAHs). Pyrene was used as a marker compound for both dermal and respiratory exposure to PAHs. The biological measure for the internal expos...

  5. Biological monitoring of polycyclic aromatic hydrocarbon exposure in a highly polluted area of Poland.

    OpenAIRE

    Ovrebø, S; Fjeldstad, P E; Grzybowska, E; Kure, E H; Chorazy, M; Haugen, A

    1995-01-01

    Air pollution in Poland and particularly in Silesia is among the worst in Europe. Many coal mines and coke oven plants are located in this area, representing a major source of carcinogenic polycyclic aromatic hydrocarbons (PAHs). We quantitated the PAH exposure level in air samples using personal sampling devices, collected urine samples from the same individuals, and measured 1-hydroxypyrene with high performance liquid chromatography. Samples were collected twice, once in February and once ...

  6. DNA adducts as a measure of lung cancer risk in humans exposed to polycyclic aromatic hydrocarbons.

    OpenAIRE

    Kriek, E; van Schooten, F.J.; Hillebrand, M J; van Leeuwen, F E; Den Engelse, L; De Looff, A J; Dijkmans, A P

    1993-01-01

    Workers in the coking, foundry, and aluminum industry can be exposed to high concentrations of polycyclic aromatic hydrocarbons (PAHs) and are at increased risk for lung cancer, as are cigarette smokers. In recent years several studies on workers in the foundry and coking industries have been reported. In these studies, white blood cell(WBC) DNA was used for analysis of PAH-DNA adducts. Theoretically, DNA adduct formation is a more relevant biological parameter for assessing exposure risk tha...

  7. Lung cancer mortality and exposure to polycyclic aromatic hydrocarbons in British coke oven workers

    OpenAIRE

    Miller, Brian G.; Doust, Emma; Cherrie, John W.; Hurley, J Fintan

    2013-01-01

    Background Workers on coke oven plants may be exposed to potentially carcinogenic polycyclic aromatic hydrocarbons (PAHs), particularly during work on the ovens tops. Two cohorts, employees of National Smokeless Fuels (NSF) and the British Steel Corporation (BSC) totalling more than 6,600 British coke plant workers employed in 1967, had been followed up to mid-1987 for mortality. Previous analyses suggested an excess in lung cancer risk of around 25%, or less when compared with Social Class I...

  8. Pollution of Flooded Arable Soils with Heavy Metals and Polycyclic Aromatic Hydrocarbons (PAHs)

    OpenAIRE

    Ciesielczuk, Tomasz; Kusza, Grzegorz; Poluszyńska, Joanna; Kochanowska, Katarzyna

    2014-01-01

    Soils that are exposed to floodwaters because of shallow groundwater and periodical wetlands are, to a large extent, exposed to contamination by organic and inorganic compounds. These are mainly compounds that have drifted along with the inflow of heavily laden floodwater and are produced within the soil profile by the anaerobic transformation of organic matter. Heavy metals and polycyclic aromatic hydrocarbon (PAH) compounds are absorbed by the soil of the floodwaters, and moving in the soil...

  9. Structural Vector Description and Estimation of Normal Boiling Points for 66 Aromatic Hydrocarbons

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    A molecular vector-type descriptor containing 6 variables is used to describe the structure of aromatic hydrocarbons (AHs) and relate to normal boiling points (bp) of AHs. The correlation coefficient (R) between the estimated bp and experimental bp is 0.9988 and the root mean square error (RMS) is 7.907° C for 66 AHs. The RMS obtained by cross-validation is 9.131° C, which implies the relationship model having good prediction ability.

  10. Tailoring ZSM-5 Zeolites for the Fast Pyrolysis of Biomass to Aromatic Hydrocarbons

    DEFF Research Database (Denmark)

    Hoff, Thomas C.; Gardner, David W.; Thilakaratne, Rajeeva;

    2016-01-01

    The production of aromatic hydrocarbons from cellulose by zeolite-catalyzed fast pyrolysis involves a complex reaction network sensitive to the zeolite structure, crystallinity, elemental composition, porosity, and acidity. The interplay of these parameters under the reaction conditions represent...... a major roadblock that has hampered significant improvement in catalyst design for over a decade. Here, we studied commercial and laboratory-synthesized ZSM-5 zeolites and combined data from 10 complementary characterization techniques in an attempt to identify parameters common to high...

  11. Detection and characterization of human serum antibodies to polycyclic aromatic hydrocarbon diol-epoxide DNA adducts.

    OpenAIRE

    Newman, M J; Light, B A; Weston, A; Tollurud, D; Clark, J L; Mann, D L; Blackmon, J P; Harris, C C

    1988-01-01

    The presence of serum antibodies to the diol-epoxide DNA adducts of representative polycyclic aromatic hydrocarbons (PAH), chrysene, benz[a]anthracene and benzo[a]pyrene, was determined by ELISA using serum samples obtained from normal healthy individuals. Antibodies that reacted against PAH adducted-DNA, but not against PAH-adducted protein, were found in the serum of approximately 40% of the test individuals. Specificity analysis of the antibodies demonstrated that serological cross-reactio...

  12. Polycyclic Aromatic Hydrocarbons Identification and Source Discrimination in Rural Soil of the Northern Persian Gulf Coast

    OpenAIRE

    Fatemeh Valizadeh-kakhki; Mohamad Pauzi Zakaria; Ahmad Zaharin Aris; Syaizwan Zahmir Zulkifli; Mehdi Mohammadi; Hasan Tajik

    2014-01-01

    Due to strategic situation of the Persian Gulf, identifying the petroleum pollution level and source is an important issue. Therefore, this paper enhanced fingerprinting method of applying biomarkers Polycyclic Aromatic Hydrocarbons (PAHs) in identifying source and distribution of oil spills of the exposed areas. 10 soil samples collected from the northern coasts of the Persian Gulf along three provinces in the south of Iran. PAH concentrations in the soil ranged from 42.76 to 5596.49 ng.g-1....

  13. Engineering of a silica encapsulation platform for hydrocarbon degradation using Pseudomonas sp. NCIB 9816-4.

    Science.gov (United States)

    Sakkos, Jonathan K; Kieffer, Daniel P; Mutlu, Baris R; Wackett, Lawrence P; Aksan, Alptekin

    2016-03-01

    Industrial application of encapsulated bacteria for biodegradation of hydrocarbons in water requires mechanically stable materials. A silica gel encapsulation method was optimized for Pseudomonas sp. NCIB 9816-4, a bacterium that degrades more than 100 aromatic hydrocarbons. The design process focused on three aspects: (i) mechanical property enhancement; (ii) gel cytocompatibility; and (iii) reduction of the diffusion barrier in the gel. Mechanical testing indicated that the compressive strength at failure (σf ) and elastic modulus (E) changed linearly with the amount of silicon alkoxide used in the gel composition. Measurement of naphthalene biodegradation by encapsulated cells indicated that the gel maintained cytocompatibility at lower levels of alkoxide. However, significant loss in activity was observed due to methanol formation during hydrolysis at high alkoxide concentrations, as measured by FTIR spectroscopy. The silica gel with the highest amount of alkoxide (without toxicity from methanol) had a biodegradation rate of 285 ± 42 nmol/L-s, σf  = 652 ± 88 kPa, and E = 15.8 ± 2.0 MPa. Biodegradation was sustained for 1 month before it dropped below 20% of the initial rate. In order to improve the diffusion through the gel, polyvinyl alcohol (PVA) was used as a porogen and resulted in a 48 ± 19% enhancement in biodegradation, but it impacted the mechanical properties negatively. This is the first report studying how the silica composition affects biodegradation of naphthalene by Pseudomonas sp. NCIB 9816-4 and establishes a foundation for future studies of aromatic hydrocarbon biodegradation for industrial application. PMID:26332745

  14. Deposition flux of aerosol particles and 15 polycyclic aromatic hydrocarbons in the North China Plain.

    Science.gov (United States)

    Wang, Xilong; Liu, Shuzhen; Zhao, Jingyu; Zuo, Qian; Liu, Wenxin; Li, Bengang; Tao, Shu

    2014-04-01

    The present study examined deposition fluxes of aerosol particles and 15 polycyclic aromatic hydrocarbons (PAHs) associated with the particles in the North China Plain. The annual mean deposition fluxes of aerosol particles and 15 PAHs were 0.69 ± 0.46 g/(m(2) ×d) and 8.5 ± 6.2 μg/(m(2) ×d), respectively. Phenanthrene, fluoranthene, pyrene, chrysene, benzo[b]fluoranthene, and benzo[k]fluoranthene were the dominant PAHs bound to deposited aerosol particles throughout the year. The total concentration of 15 PAHs in the deposited aerosol particles was the highest in winter but lowest in spring. The highest PAH concentration in the deposited aerosol particles in winter was because the heating processes highly increased the concentration in atmospheric aerosol particles. Low temperature and weak sunshine in winter reduced the degradation rate of deposited aerosol particle-bound PAHs, especially for those with low molecular weight. The lowest PAH concentration in deposited aerosol particles in spring resulted from the frequently occurring dust storms, which diluted PAH concentrations. The mean deposition flux of PAHs with aerosol particles in winter (16 μg/[m(2) ×d]) reached 3 times to 5 times that in other seasons (3.5-5.0 μg/[m(2) ×d]). The spatial variation of the deposition flux of PAHs with high molecular weight (e.g., benzo[a]pyrene) was consistent with their concentrations in the atmospheric aerosol particles, whereas such a phenomenon was not observed for those with low molecular weight (e.g., phenanthrene) because of their distinct hydrophobicity, Henry's law constant, and the spatially heterogeneous meteorological conditions.

  15. Irradiated sewage sludge for increased crop production - I. Pathogens and polycyclic aromatic hydrocarbons

    International Nuclear Information System (INIS)

    Samples of raw sewage and sewage sludge, and of fruits and nuts were collected from El-Gabal El-Asfar farm for determination of their pathogen contents. The dominant viable bacterium in the sludge and sewage water was Escherichia coli. Bacteria were present in the water phase in much lower counts than in the sludge. Fruits taken from orchards irrigated with raw sewage showed no detectable internal contamination with bacteria, parasites, or viruses. Gamma irradiation reduced pathogen density significantly. The E. coli counts in sludge decreased from 109 CFU/L to nil with a dose of 6 kGy, and from 106 CFU/L to nil at a dose of 1 kGy for sewage water. The vegetative forms of unicellular parasites disappeared at 6 kGy and 1 kGy for sludge and sewage water, respectively. The the dose required for 90% reduction in bacterial count (D10)) was 0.67 kGy and 0.17 kGy for sludge and sewage water, respectively. It was concluded 6 kGy is appropriate for sludge, whereas the water phase requires only 1 kGy for decontamination, probably due to the dilution effect. The effect of gamma radiation on degradation of toxic organic pollutants in dry and moist sludges was investigated. Thirteen polycyclic aromatic hydrocarbons (PAHs) were identified in sludge. Non-irradiated moist sludge showed total PAHs of 29 mg/kg, whereas dry sludge contained 5.4 mg/kg. Gamma irradiation reduced PAH content by 53 to 75% for the moist sludge, and 26 to 63% for the dry sludge for doses of 2 to 10 kGy, respectively. (author)

  16. Shifts in microbial community structure during in situ surfactant-enhanced bioremediation of polycyclic aromatic hydrocarbon-contaminated soil.

    Science.gov (United States)

    Wang, Lingwen; Li, Feng; Zhan, Yu; Zhu, Lizhong

    2016-07-01

    This study aims to reveal the microbial mechanism of in situ surfactant-enhanced bioremediation (SEBR). Various concentrations of rhamnolipids, Tween 80, and sodium dodecyl benzenesulfonate (SDBS) were separately sprayed onto soils contaminated with polycyclic aromatic hydrocarbons (PAHs) for years. Within 90 days, the highest level of degradation (95 %) was observed in the soil treated with rhamnolipids (10 mg/kg), followed by 92 % degradation with Tween 80 (50 mg/kg) and 90 % degradation with SDBS (50 mg/kg). The results of the microbial phospholipid fatty acids (PLFAs) suggest that bacteria dominated the enhanced PAH biodegradation (94 % of the maximum contribution). The shift of bacterial community structure during the surfactant treatment was analyzed by using the 16S rRNA gene high-throughput sequencing. In the presence of surfactants, the number of the operational taxonomic units (OTUs) associated with Bacillus, Pseudomonas, and Sphingomonas increased from 2-3 to 15-30 % at the end of the experiment (two to three times of control). Gene prediction with phylogenetic investigation of communities by reconstruction of unobserved states (PICRUSt) shows that the PAH-degrading genes, such as 1-hydroxy-2-naphthoate dioxygenase and PAH dioxygenase large subunit, significantly increased after the surfactant applications (p bioremediation.

  17. Shifts in microbial community structure during in situ surfactant-enhanced bioremediation of polycyclic aromatic hydrocarbon-contaminated soil.

    Science.gov (United States)

    Wang, Lingwen; Li, Feng; Zhan, Yu; Zhu, Lizhong

    2016-07-01

    This study aims to reveal the microbial mechanism of in situ surfactant-enhanced bioremediation (SEBR). Various concentrations of rhamnolipids, Tween 80, and sodium dodecyl benzenesulfonate (SDBS) were separately sprayed onto soils contaminated with polycyclic aromatic hydrocarbons (PAHs) for years. Within 90 days, the highest level of degradation (95 %) was observed in the soil treated with rhamnolipids (10 mg/kg), followed by 92 % degradation with Tween 80 (50 mg/kg) and 90 % degradation with SDBS (50 mg/kg). The results of the microbial phospholipid fatty acids (PLFAs) suggest that bacteria dominated the enhanced PAH biodegradation (94 % of the maximum contribution). The shift of bacterial community structure during the surfactant treatment was analyzed by using the 16S rRNA gene high-throughput sequencing. In the presence of surfactants, the number of the operational taxonomic units (OTUs) associated with Bacillus, Pseudomonas, and Sphingomonas increased from 2-3 to 15-30 % at the end of the experiment (two to three times of control). Gene prediction with phylogenetic investigation of communities by reconstruction of unobserved states (PICRUSt) shows that the PAH-degrading genes, such as 1-hydroxy-2-naphthoate dioxygenase and PAH dioxygenase large subunit, significantly increased after the surfactant applications (p < 0.05). The findings of this study provide insights into the surfactant-induced shifts of microbial community, as well as critical factors for efficient bioremediation. PMID:27068902

  18. Geochemical markers and polycyclic aromatic hydrocarbons in solvent extracts from diesel engine particulate matter.

    Science.gov (United States)

    Fabiańska, Monika; Kozielska, Barbara; Bielaczyc, Piotr; Woodburn, Joseph; Konieczyński, Jan

    2016-04-01

    Exhaust particulate from compression ignition (CI) engines running on engine and chassis dynamometers was studied. Particulate dichloromethane extracts were qualitatively and quantitatively analyzed for polycyclic aromatic hydrocarbons (PAHs) and biomarkers by gas chromatography with flame ionization detector (GC-FID) and gas chromatography-mass spectrometry (GC-MS). PAH group profiles were made and the PAH group shares according to the number of rings (2 or 3; 4; 5 or more) as well as diagnostic indices were calculated. Values of geochemical ratios of selected biomarkers and alkyl aromatic hydrocarbons were compared with literature values. A geochemical interpretation was carried out using these values and biomarker and alkyl aromatic hydrocarbon distributions. It has been shown that geochemical features are unequivocally connected to the emission of fossil fuels and biofuels burned in CI engines. The effect of the exothermic combustion process is limited to low-molecular-weight compounds, which shows that the applied methodology permits source identification of PAHs coexisting in the particulate emitted. PMID:26728284

  19. MODELING GALACTIC EXTINCTION WITH DUST AND 'REAL' POLYCYCLIC AROMATIC HYDROCARBONS

    Energy Technology Data Exchange (ETDEWEB)

    Mulas, Giacomo; Casu, Silvia; Cecchi-Pestellini, Cesare [INAF-Osservatorio Astronomico di Cagliari, Strada n.54, Loc. Poggio dei Pini, I-09012 Capoterra (Italy); Zonca, Alberto, E-mail: gmulas@oa-cagliari.inaf.it, E-mail: silvia@oa-cagliari.inaf.it, E-mail: ccp@oa-cagliari.inaf.it, E-mail: azonca@oa-cagliari.inaf.it [Dipartimento di Fisica, Universita di Cagliari, Strada Prov.le Monserrato-Sestu Km 0.700, I-09042 Monserrato (Italy)

    2013-07-01

    We investigate the remarkable apparent variety of galactic extinction curves by modeling extinction profiles with core-mantle grains and a collection of single polycyclic aromatic hydrocarbons. Our aim is to translate a synthetic description of dust into physically well-grounded building blocks through the analysis of a statistically relevant sample of different extinction curves. All different flavors of observed extinction curves, ranging from the average galactic extinction curve to virtually 'bumpless' profiles, can be described by the present model. We prove that a mixture of a relatively small number (54 species in 4 charge states each) of polycyclic aromatic hydrocarbons can reproduce the features of the extinction curve in the ultraviolet, dismissing an old objection to the contribution of polycyclic aromatic hydrocarbons to the interstellar extinction curve. Despite the large number of free parameters (at most the 54 Multiplication-Sign 4 column densities of each species in each ionization state included in the molecular ensemble plus the 9 parameters defining the physical properties of classical particles), we can strongly constrain some physically relevant properties such as the total number of C atoms in all species and the mean charge of the mixture. Such properties are found to be largely independent of the adopted dust model whose variation provides effects that are orthogonal to those brought about by the molecular component. Finally, the fitting procedure, together with some physical sense, suggests (but does not require) the presence of an additional component of chemically different very small carbonaceous grains.

  20. Soil sealing degree as factor influencing urban soil contamination with polycyclic aromatic hydrocarbons (PAHs

    Directory of Open Access Journals (Sweden)

    Mendyk Łukasz

    2016-03-01

    Full Text Available The objective of the study was to determine role of soil sealing degree as the factor influencing soil contamination with polycyclic aromatic hydrocarbons (PAHs. The study area included four sampling sites located within the administrative boundaries of the Toruń city, Poland. Sampling procedure involved preparing soil pits representing three examples of soil sealing at each site: non-sealed soil as a control one (I and two degrees of soil sealing: semi-pervious surface (II and totally impervious surface (III. Together with basic properties defined with standard procedures (particle size distribution, pH, LOI, content of carbonates content of selected PAHs was determined by dichloromethane extraction using gas chromatography with mass spectrometric detection (GC-MS. Obtained results show that urban soils in the city of Toruń are contaminated with polycyclic aromatic hydrocarbons. Soil sealing degree has a strong influence on the soil contamination with polycyclic aromatic hydrocarbons. Totally sealed soils are better preserved from atmospheric pollution including PAHs. Combustion of grass/wood/coal was the main source of determined PAHs content in examined soils.

  1. DISTRIBUTION AND CHARACTERIZATION OF POLYCYCLIC AROMATIC HYDROCARBON COMPOUNDS IN AIRBORNE PARTICULATES OF EAST ASIA

    Institute of Scientific and Technical Information of China (English)

    Yan Liu; Libin Liu; Jin-Ming Lin; Ning Tang; Kazuichi Hayakawa

    2006-01-01

    A review is presented on the distribution and characterization of polycyclic aromatic hydrocarbons (PAHs)and their derivatives, including nitro-PAHs and hydro-PAHs, on atmospheric particulates of East Asia. Generally, PAH compounds with two or three aromatic rings are released mainly into the gas phase, while those containing three or more aromatic rings are associated with particulate matter (PM) emission. Particle-associated PAHs are primarily adsorbed on fine particles, and little associated with coarse particles. Investigation into the concentration level of PAHs in different areas can serve not only to reflect the pollutant status and sources but also to lead to the formulation of control strategies.The results of the present study show that China has more severe PAH pollution than such East Asian countries as Japan and Korea.

  2. Impact of molecular structure on secondary organic aerosol formation from aromatic hydrocarbon photooxidation under low-NOx conditions

    Science.gov (United States)

    Li, Lijie; Tang, Ping; Nakao, Shunsuke; Cocker, David R., III

    2016-08-01

    The molecular structure of volatile organic compounds determines their oxidation pathway, directly impacting secondary organic aerosol (SOA) formation. This study comprehensively investigates the impact of molecular structure on SOA formation from the photooxidation of 12 different eight- to nine-carbon aromatic hydrocarbons under low-NOx conditions. The effects of the alkyl substitute number, location, carbon chain length and branching structure on the photooxidation of aromatic hydrocarbons are demonstrated by analyzing SOA yield, chemical composition and physical properties. Aromatic hydrocarbons, categorized into five groups, show a yield order of ortho (o-xylene and o-ethyltoluene) > one substitute (ethylbenzene, propylbenzene and isopropylbenzene) > meta (m-xylene and m-ethyltoluene) > three substitute (trimethylbenzenes) > para (p-xylene and p-ethyltoluene). SOA yields of aromatic hydrocarbon photooxidation do not monotonically decrease when increasing alkyl substitute number. The ortho position promotes SOA formation while the para position suppresses aromatic oxidation and SOA formation. Observed SOA chemical composition and volatility confirm that higher yield is associated with further oxidation. SOA chemical composition also suggests that aromatic oxidation increases with increasing alkyl substitute chain length and branching structure. Further, carbon dilution conjecture developed by Li et al. (2016) is extended in this study to serve as a standard method to determine the extent of oxidation of an alkyl-substituted aromatic hydrocarbon.

  3. Aliphatic and aromatic hydrocarbons in particulate fallout of Alexandria, Egypt: Sources and implications

    Energy Technology Data Exchange (ETDEWEB)

    Aboul-Kassim, T.A.T.; Simoneit, B.R.T. [Oregon State Univ., Corvallis, OR (United States)

    1995-10-01

    Particulate fallout samples (PFS) were collected in Alexandria, and their aliphatic and aromatic hydrocarbon compositions were determined both quantitatively and qualitatively to characterize the homologous and biomarker compounds in terms of their original sources. The results show that all samples contain aliphatic hydrocarbons, including n-alkanes, UCM, isoprenoids, tri- and tetracyclic terpanes, hopanes, and steranes/diasteranes. The main source of these compounds is from petrochemical contamination with trace input of terrestrial higher plant wax. In addition, polycyclic aromatic hydrocarbons, which are considered to be combustion products from fossil fuels such as petroleum, are also widely distributed in all samples. Multivariate statistical analysis, including extended Q-mode factor analysis and linear programming technique, was performed in order to reduce the hydrocarbon data set into a meaningful number of end members (sources). This analysis indicates that there are two significant end members explaining 90% of the total variation among the samples and confirming petrochemical (79.6%), and thermogenic/pyrolytic (10.4%) sources in the PFS model. 65 refs., 7 figs., 4 tabs.

  4. Formation of Polycyclic Aromatic Hydrocarbons and Nitrogen Containing Polycyclic Aromatic Compounds in Titan's Atmosphere, the Interstellar Medium and Combustion

    Science.gov (United States)

    Landera, Alexander

    2013-12-01

    Several different mechanisms leading to the formation of (substituted) naphthalene and azanaphthalenes were examined using theoretical quantum chemical calculations. As a result, a series of novel synthetic routes to Polycyclic Aromatic Hydrocarbons (PAHs) and Nitrogen Containing Polycyclic Aromatic Compounds (N-PACs) have been proposed. On Earth, these aromatic compounds originate from incomplete combustion and are released into our environment, where they are known to be major pollutants, often with carcinogenic properties. In the atmosphere of a Saturn's moon Titan, these PAH and N-PACs are believed to play a critical role in organic haze formation, as well as acting as chemical precursors to biologically relevant molecules. The theoretical calculations were performed by employing the ab initio G3(MP2,CC)/B3LYP/6-311G** method to effectively probe the Potential Energy Surfaces (PES) relevant to the PAH and N-PAC formation. Following the construction of the PES, Rice-Ramsperger-Kassel-Markus (RRKM) theory was used to evaluate all unimolecular rate constants as a function of collision energy under single-collision conditions. Branching ratios were then evaluated by solving phenomenological rate expressions for the various product concentrations. The most viable pathways to PAH and N-PAC formation were found to be those where the initial attack by the ethynyl (C2H) or cyano (CN) radical toward a unsaturated hydrocarbon molecule led to the formation of an intermediate which could not effectively lose a hydrogen atom. It is not until ring cyclization has occurred, that hydrogen elimination leads to a closed shell product. By quenching the possibility of the initial hydrogen atom elimination, one of the most competitive processes preventing the PAH or N-PAC formation was avoided, and the PAH or N-PAC formation was allowed to proceed. It is concluded that these considerations should be taken into account when attempting to explore any other potential routes towards

  5. Relating desorption of polycyclic aromatic hydrocarbons from harbour sludges to type of organic material

    Science.gov (United States)

    Heister, K.; Pols, S.; Loch, J. P. G.; Bosma, T.

    2009-04-01

    For decades, polycyclic aromatic hydrocarbons (PAH) cause great concern as environmental pollutants. Especially river and marine harbour sediments are frequently polluted with PAH derived from surface runoff, fuel and oil spills due to shipping and industrial activities, industrial waste and atmospheric deposition. Harbour sediments contain large amounts of organic carbon and clay minerals and are therefore not easy to remediate and have to be stored in sludge depositories after dredging to maintain sufficient water depth for shipping. The organic contaminants will be adsorbed to particles, leached in association with dissolved organic material or microbially degraded. However, compounds of high molecular weight are very persistent, particularly under anaerobic conditions, thus giving rise to the potential to become desorbed again. PAH adsorb mainly to organic material. It has been shown that components of the organic material with a low polarity and a high hydrophobicity like aliphatic and aromatic components exhibit a high sorption capacity for hydrophobic organic contaminants like PAH. Accordingly, not only the amount but also the type of organic material needs to be determined in order to be able to predict contaminant behaviour. In this study, desorption behaviour of the 16 EPA-PAH in two different harbour sludges from the port of Rotterdam, the Netherlands, has been investigated. The Beerkanaal (BK) site is located relatively close to the North Sea and represents a brackish environment; the Beneden Merwede River (BMR) site originates from a fresh water environment and is close to industrial sites. The samples were placed in dialysis membranes and brought into contact with water for a period of 130 days. At several time intervals, water samples were retrieved for analysis of pH, dissolved organic carbon (DOC) content, electrical conductivity and PAH concentrations. The experiment was conducted at 4 and at 20°C. Although the samples were initially treated with

  6. Candidates for the development of consortia capable of petroleum hydrocarbon degradation in marine environment

    Digital Repository Service at National Institute of Oceanography (India)

    David, J.; Gupta, R.; Mohandass, C.; Nair, S.; LokaBharathi, P.A.; Chandramohan, D.

    strains were found to degrade crude oil. Some of the bacterial strains could degrade more than 90% of the aliphatic fractions and more than 50% of the aromatic component. These could also oxidize pure aromatics like naphthalene (80%) and anthracene (55...

  7. Degradation and assimilation of aromatic compounds by Corynebacterium glutamicum: another potential for applications for this bacterium?

    Science.gov (United States)

    Shen, Xi-Hui; Zhou, Ning-Yi; Liu, Shuang-Jiang

    2012-07-01

    With the implementation of the well-established molecular tools and systems biology techniques, new knowledge on aromatic degradation and assimilation by Corynebacterium glutamicum has been emerging. This review summarizes recent findings on degradation of aromatic compounds by C. glutamicum. Among these findings, the mycothiol-dependent gentisate pathway was firstly discovered in C. glutamicum. Other important knowledge derived from C. glutamicum would be the discovery of linkages among aromatic degradation and primary metabolisms such as gluconeogenesis and central carbon metabolism. Various transporters in C. glutamicum have also been identified, and they play an essential role in microbial assimilation of aromatic compounds. Regulation on aromatic degradation occurs mainly at transcription level via pathway-specific regulators, but global regulator(s) is presumably involved in the regulation. It is concluded that C. glutamicum is a very useful model organism to disclose new knowledge of biochemistry, physiology, and genetics of the catabolism of aromatic compounds in high GC content Gram-positive bacteria, and that the new physiological properties of aromatic degradation and assimilation are potentially important for industrial applications of C. glutamicum.

  8. Current-voltage characteristics of a homologous series of polycyclic aromatic hydrocarbons.

    Science.gov (United States)

    Böhme, Thilo; Simpson, Christopher D; Müllen, Klaus; Rabe, Jürgen P

    2007-01-01

    A novel alkyl-substituted polycyclic aromatic hydrocarbon (PAH) with D(2h) symmetry and 78 carbon atoms in the aromatic core (C78) was synthesized, thereby completing a homologous series of soluble PAH compounds with increasing size of the aromatic pi system (42, 60, and 78 carbon atoms). The optical band gaps were determined by UV/Vis and fluorescence spectroscopy in solution. Scanning tunneling microscopy (STM) and spectroscopy (STS) revealed diode-like current versus voltage (I-V) characteristics through individual aromatic cores in monolayers at the interface between the solution and the basal plane of graphite. The asymmetry of the current-voltage (I-V) characteristics increases with the increasing size of the aromatic core, and the concomitantly decreasing HOMO-LUMO gap. This is attributed to resonant tunneling through the HOMO of the adsorbed molecule, and an asymmetric position of the molecular species in the tunnel junction. Consistently, submolecularly resolved STM images at negative substrate bias are in good agreement with the calculated pattern for the electron densities of the HOMOs. The analysis provides the basis for tailoring rectification with a single molecule in an STM junction. PMID:17579898

  9. Fate of polycyclic aromatic hydrocarbons (PAH) in the rhizosphere and myco-rhizosphere

    International Nuclear Information System (INIS)

    Organic pollutants such as polycyclic aromatic hydrocarbons (PAH) can reach high concentrations in soils due to man-made pollution related to industrial, agricultural or urban activities. Such concentrations can reach toxic values and create major environmental and health problems. One of the first entry point of pollutants in plant ecosystems is the rhizosphere, defined as the soil under the influence of roots. In the rhizosphere, the plant release root exudates, feeding soil microorganisms, and take up water and nutrients. Among the rhizosphere inhabitants, arbuscular mycorrhizal (AM) fungi are ubiquitous root symbiotic fungi, contributing to plant growth and plant nutrition. In PAH-polluted soils, biodegradation of PAH increases, which is attributed to increased microbial activity in the rhizosphere..We studied the contribution of the rhizosphere of mycorrhizal and non-mycorrhizal plants to the biodegradation of PAH in the rhizosphere, taking into account microbial community structure. Different experiments were performed with industrial contaminated soils and PAH-spiked soils, in pot cultures as well as compartmented devices allowing to analyze rhizosphere processes in consecutive sections as a function of distance to roots. Clover and ryegrass, inoculated or not with the arbuscular mycorrhizal fungus Glomus mosseae were used.. After different time periods, plants were harvested, biomass and mycorrhizal root colonization were estimated. Microbial Density of microbial heterotrophs and of degrading bacteria was estimated by MPN techniques in micro-plates. Microbial community structure was estimated by DNA extraction from the rhizosphere, amplification by PCR and analysed by TGGE (temperature gradient gel electrophoresis), or by PLFA (phospholipid fatty acid analysis). PAH in soil were extracted by Soxhlet and analysed by GC-MS. We showed that the concentration of PAH increased with the distance to roots (Corgie et al, 2003) and was lower in the myco

  10. Mineralization of polycyclic aromatic hydrocarbons by the white rot fungus Pleurotus ostreatus

    Energy Technology Data Exchange (ETDEWEB)

    Bezalel, L.; Hadar, Y. [Hebrew Univ. of Jerusalem, Rehovot (Israel); Cerniglia, C.E. [National Center for Toxicological Research, Jefferson, AR (United States)

    1996-01-01

    White rot fungi, including Pleurotus ostreatus, have the ability to efficiently degrade lignin, a naturally occurring aromatic polymer. Previous work has found these organisms were able to degrade PAHs and in some cases to mineralize them; most of the work was done with Phanerochaete chrysosporium. P. ostreatus differs from P. chrysosporium in its lignin degradation mechanism. In this study, enzymatic activities were monitored during P. ostreatus growth in the presence of PAHs and the fungus`s ability to mineralize catechol and various PAHs was demonstrated. 29 refs., 3 figs., 1 tab.

  11. Microbial degradation of aliphatic and aliphatic-aromatic co-polyesters.

    Science.gov (United States)

    Shah, Aamer Ali; Kato, Satoshi; Shintani, Noboru; Kamini, Numbi Ramudu; Nakajima-Kambe, Toshiaki

    2014-04-01

    Biodegradable plastics (BPs) have attracted much attention since more than a decade because they can easily be degraded by microorganisms in the environment. The development of aliphatic-aromatic co-polyesters has combined excellent mechanical properties with biodegradability and an ideal replacement for the conventional nondegradable thermoplastics. The microorganisms degrading these polyesters are widely distributed in various environments. Although various aliphatic, aromatic, and aliphatic-aromatic co-polyester-degrading microorganisms and their enzymes have been studied and characterized, there are still many groups of microorganisms and enzymes with varying properties awaiting various applications. In this review, we have reported some new microorganisms and their enzymes which could degrade various aliphatic, aromatic, as well as aliphatic-aromatic co-polyesters like poly(butylene succinate) (PBS), poly(butylene succinate)-co-(butylene adipate) (PBSA), poly(ε-caprolactone) (PCL), poly(ethylene succinate) (PES), poly(L-lactic acid) (PLA), poly(3-hydroxybutyrate) and poly(3-hydoxybutyrate-co-3-hydroxyvalterate) (PHB/PHBV), poly(ethylene terephthalate) (PET), poly(butylene terephthalate) (PBT), poly(butylene adipate-co-terephthalate (PBAT), poly(butylene succinate-co-terephthalate) (PBST), and poly(butylene succinate/terephthalate/isophthalate)-co-(lactate) (PBSTIL). The mechanism of degradation of aliphatic as well as aliphatic-aromatic co-polyesters has also been discussed. The degradation ability of microorganisms against various polyesters might be useful for the treatment and recycling of biodegradable wastes or bioremediation of the polyester-contaminated environments. PMID:24522729

  12. Isolation and Characterization of Hydrocarbon-Degrading Yeast Strains from Petroleum Contaminated Industrial Wastewater

    OpenAIRE

    Boutheina Gargouri; Najla Mhiri; Fatma Karray; Fathi Aloui; Sami Sayadi

    2015-01-01

    Two yeast strains are enriched and isolated from industrial refinery wastewater. These strains were observed for their ability to utilize several classes of petroleum hydrocarbons substrates, such as n-alkanes and aromatic hydrocarbons as a sole carbon source. Phylogenetic analysis based on the D1/D2 variable domain and the ITS-region sequences indicated that strains HC1 and HC4 were members of the genera Candida and Trichosporon, respectively. The mechanism of hydrocarbon uptaking by yeast, ...

  13. Methyl-β-cyclodextrin enhanced biodegradation of polycyclic aromatic hydrocarbons and associated microbial activity in contaminated soil

    Institute of Scientific and Technical Information of China (English)

    Mingming Sun; Yongming Luo; Peter Christie; Zhongjun Jia; Zhengao Li; Ying Teng

    2012-01-01

    The contamination of soils by polycyclic aromatic hydrocarbons (PAHs) is a widespread environmental problem and the remediation of PAHs from these areas has been a major concern.The effectiveness of many in situ bioremediation systems may be constrained by low contaminant bipavailability due to limited aqueous solubility or a large magnitude of sorption.The objective of this research was to evaluate the effect of methyl-β-cyclodextrin (MCD) on bioaugmentation by Paracoccus sp.strain HPD-2 of an aged PAH-contaminated soil.When 10% (W/W) MCD amendment was combined with bioaugmentation by the PAH-degrading bacterium Paracoccus sp.strain HPD-2,the percentage degradation of total PAHs was significantly enhanced up to 34.8%.Higher counts of culturable PAH-degrading bacteria and higher soil dehydrogenase and soil polyphenol oxidase activities were observed in 10% (W/W) MCD-assisted bioaugmentation soil.This MCD-assisted bioaugmentation strategy showed significant increases (p < 0.05) in the average well color development (AWCD) obtained by the BIOLOG Eco plate assay,Shannon-Weaver index (H) and Simpson index (λ) compared with the controls,implying that this strategy at least partially restored the microbiological functioning of the PAH-contaminated soil.The results suggest that MCD-aided bioaugmentation by Paracoccus sp.strain HPD-2 may be a promising practical bioremediation strategy for aged PAH-contaminated soils.

  14. Application of the cubic-plus-association (CPA) equation of state to complex mixtures with aromatic hydrocarbons

    DEFF Research Database (Denmark)

    Folas, Georgios; Kontogeorgis, Georgios; Michelsen, Michael Locht;

    2006-01-01

    The cubic-plus-association (CPA) equation of state is applied to phase equilibria of mixtures containing alcohols, glycols, water, and aromatic or olefinic hydrocarbons. Previously, CPA has been successfully used for mixtures containing various associating compounds (alcohols, glycols, amines......, organic acids, and water) and aliphatic hydrocarbons. We show in this work that the model can be satisfactorily extended to complex vapor-liquid-liquid equilibria with aromatic or olefinic hydrocarbons. The solvation between aromatics/olefinics and polar compounds is accounted for. This is particularly...... important for mixtures containing water and glycols, but less so for mixtures with alcohols. For water/hydrocarbons, a single binary interaction parameter which accounts for the solvation is fitted to the experimental liquid-liquid equilibria (LLE) data. The interaction parameter of the physical term...

  15. Global distribution and Gas-particle Partitioning of Polycyclic Aromatic Hydrocarbons - a Modelling Study

    Science.gov (United States)

    Lammel, G.; Sehili, A. M.

    2009-04-01

    Polycyclic aromatic hydrocarbons (PAHs) are emitted in all combustion processes. Some undergo re-volatilisation (multi-hopping). Little is known about degradation pathways and the processes determining gas-particle partitioning (Lohmann & Lammel, 2004). Distribution and fate have no been studied on the global scale so far (except for emissions in Europe and Russia; Sehili & Lammel, 2007). Anthracene (ANT), fluoranthene (FLT) and benzo[a]pyrene (BAP) have been studied under present-day climate and each 3 scenarios of atmospheric degradation and gas-particle partitioning using an atmospheric general circulation model with embedded dynamic aerosol submodel, ECHAM-HAM (Stier et al., 2005) and re-volatilization from ground compartments (Semeena et al., 2006). 10 years were simulated with a time-step of 30 min and 2.8°x2.8° and 19 levels. Emissions were compiled based on emission factors in 27 major types of combustion technologies, scaled to 141 combustion technologies and their global distribution as of 1996 (1°x1°) according to fuel type and the PM1 emission factor (Bond et al., 2004). The emissions were entried uniformly throughout the entire simulation time. Scenarios tested: AD = adsorption (according to the Junge empirical relationship; Pankow, 1987), OB = absorption in organic matter and adsorption to soot (Lohmann & Lammel, 2004) without and DP = with degradation in the atmospheric particulate phase. Gas-particle partitioning in air influences drastically the atmospheric cycling, total environmental fate (e.g. compartmental distributions) and the long-range transport potential (LRTP) of the substances studied. The LRTP is mostly regional. Comparison with observed levels indicate that degradation in the particulate phase must be slower than in the gas-phase. Furthermore, the levels of semivolatile PAHs (ANT and FLT) at high latitudes and a European mid latitude site cannot be explained by partitioning due to adsorption alone, but point to both absorption into

  16. C-H and N-H bond dissociation energies of small aromatic hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Barckholtz, C.; Barckholtz, T.A.; Hadad, C.M.

    1999-01-27

    A survey of computational methods was undertaken to calculate the homolytic bond dissociation energies (BDEs) of the C-H and N-H bonds in monocyclic aromatic molecules that are representative of the functionalities present in coal. These include six-membered rings (benzene, pyridine, pyridazine, pyrimidine, pyrazine) and five-membered rings (furan, thiophene, pyrrole, oxazole). By comparison of the calculated C-H BDEs with the available experimental values for these aromatic molecules, the B3LYP/6-31G(d) level of theory was selected to calculate the BDEs of polycyclic aromatic hydrocarbons (PAHs), including carbonaceous PAHs (naphthalene, anthracene, pyrene, coronene) and heteroatomic PAHs (benzofuran, benzothiophene, indole, benzoxazole, quinoline, isoquinoline, dibenzofuran, carbazole). The cleavage of a C-H or a N-H bond generates a {sigma} radical that is, in general, localized at the site from which the hydrogen atom was removed. However, delocalization of the unpaired electron results in {approximately} 7 kcal {center{underscore}dot} mol{sup {minus}1} stabilization of the radical with respect to the formation of phenyl when the C-H bond is adjacent to a nitrogen atom in the azabenzenes. Radicals from five-membered rings are {approximately} 6 kcal {center{underscore}dot} mol{sup {minus}1} less stable than those formed from six-membered rings due to both localization of the spin density and geometric factors. The location of the heteroatoms in the aromatic ring affects the C-H bond strengths more significantly than does the size of the aromatic network. Therefore, in general, the monocyclic aromatic molecules can be used to predict the C-H BDE of the large PAHs within 1 kcal {center{underscore}dot} mol{sup {minus}1}.

  17. Distribution and Geochemical Implication of Aromatic Hydrocarbons across the Meishan Permian-Triassic Boundary

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Aromatic compounds extracted from sedimentary rocks can reflect environmental conditions, organic sources and maturity. The aromatics, identified in association with mass extinction in particular, would provide a signature assisting our understanding of the causes of the biotic crisis. Aromatic hydrocarbons were fractionated from the total lipid extracts of 37 samples taken from the Permian Triassic boundary (beds 23 to 34) of section B at Meishan(煤山),Zhejiang(浙江)Province in South China. These aromatics were analyzed by using gas chromatography-mass spectrometry (GC-MS). Main compounds identified include naphthalene, phenanthrenes, fluorene, dibenzothiophene, dibenzofuran, fluoranthene, pyrene and some of their methyl homologues. The indices of methyl phenanthrene distribution fraction indicate the comparable maturity (within the oil window, 0.7% - 1.0% of the mean vitrinite reflectance) of the organic matter throughout the whole profile analyzed. The ratio of dibenzothiophene to phenanthrene (DBT/PHN) varies generally at a comparable pace with lithology. Significantly,a gradual decrease of this ratio was observed within bed 24 limestone, which is probably due to the variation of sedimentary environment. This change is in line with the drop in the carbon isotope composition of carbonate, the loss of the Changhsingian reef ecosystem, and the decrease of cyanobacteria abundance within the bacteria population. The coincidence of these records suggests a close relation between the biotic crisis and marine environmental conditions, and these records clearly show the onset of the biotic crisis prior to event bed 25.

  18. Laboratory studies of polycyclic aromatic hydrocarbons: the search for interstellar candidates

    CERN Document Server

    Joblin, C; Simon, A; Mulas, G

    2009-01-01

    Polycyclic Aromatic Hydrocarbons (PAHs) are considered as a major constituent of interstellar dust. They have been proposed as the carriers of the Aromatic Infrared Bands (AIBs) observed in emission in the mid-IR. They likely have a significant contribution to various features of the extinction curve such as the 220 nm bump,the far-UV rise and the diffuse interstellar bands. Emission bands are also expected in the far-IR, which are better fingerprints of molecular identity than the AIBs. They will be searched for with the Herschel Space Observatory. Rotational emission is also expected in the mm range for those molecules which carry significant dipole moments. Despite spectroscopic studies in the laboratory, no individual PAH species could be identified. This emphasises the need for an investigation on where interstellar PAHs come from and how they evolve due to environmental conditions: ionisation and dissociation upon UV irradiation, interactions with electrons, gas and dust. There is also evidence for PAH ...

  19. Understanding the Reactivity of Planar Polycyclic Aromatic Hydrocarbons: Towards the Graphene Limit.

    Science.gov (United States)

    García-Rodeja, Yago; Solà, Miquel; Fernández, Israel

    2016-07-18

    The Diels-Alder reactivity of maleic anhydride towards the bay regions of planar polycyclic aromatic hydrocarbons was explored computationally in the DFT framework. The process becomes more and more exothermic and the associated activation barriers become lower and lower when the size of the system increases. This enhanced reactivity follows an exponential behavior that reaches its maximum for systems having 18-20 benzenoid rings in their structures. This peculiar behavior was analyzed in detail by using the activation strain model of reactivity in combination with energy decomposition analysis. The influence of the change in the aromaticity of the polycyclic compound during the process on the respective activation barriers was also studied. PMID:27304921

  20. Magnetic ionic liquids as non-conventional extraction solvents for the determination of polycyclic aromatic hydrocarbons.

    Science.gov (United States)

    Trujillo-Rodríguez, María J; Nacham, Omprakash; Clark, Kevin D; Pino, Verónica; Anderson, Jared L; Ayala, Juan H; Afonso, Ana M

    2016-08-31

    This work describes the applicability of magnetic ionic liquids (MILs) in the analytical determination of a group of heavy polycyclic aromatic hydrocarbons. Three different MILs, namely, benzyltrioctylammonium bromotrichloroferrate (III) (MIL A), methoxybenzyltrioctylammonium bromotrichloroferrate (III) (MIL B), and 1,12-di(3-benzylbenzimidazolium) dodecane bis[(trifluoromethyl)sulfonyl)]imide bromotrichloroferrate (III) (MIL C), were designed to exhibit hydrophobic properties, and their performance examined in a microextraction method for hydrophobic analytes. The magnet-assisted approach with these MILs was performed in combination with high performance liquid chromatography and fluorescence detection. The study of the extraction performance showed that MIL A was the most suitable solvent for the extraction of polycyclic aromatic hydrocarbons and under optimum conditions the fast extraction step required ∼20 μL of MIL A for 10 mL of aqueous sample, 24 mmol L(-1) NaOH, high ionic strength content of NaCl (25% (w/v)), 500 μL of acetone as dispersive solvent, and 5 min of vortex. The desorption step required the aid of an external magnetic field with a strong NdFeB magnet (the separation requires few seconds), two back-extraction steps for polycyclic aromatic hydrocarbons retained in the MIL droplet with n-hexane, evaporation and reconstitution with acetonitrile. The overall method presented limits of detection down to 5 ng L(-1), relative recoveries ranging from 91.5 to 119%, and inter-day reproducibility values (expressed as relative standard derivation) lower than 16.4% for a spiked level of 0.4 μg L(-1) (n = 9). The method was also applied for the analysis of real samples, including tap water, wastewater, and tea infusion. PMID:27506350

  1. Methanogenic degradation of petroleum hydrocarbons in subsurface environments remediation, heavy oil formation, and energy recovery.

    Science.gov (United States)

    Gray, N D; Sherry, A; Hubert, C; Dolfing, J; Head, I M

    2010-01-01

    Hydrocarbons are common constituents of surface, shallow, and deep-subsurface environments. Under anaerobic conditions, hydrocarbons can be degraded to methane by methanogenic microbial consortia. This degradation process is widespread in the geosphere. In comparison with other anaerobic processes, methanogenic hydrocarbon degradation is more sustainable over geological time scales because replenishment of an exogenous electron acceptor is not required. As a consequence, this process has been responsible for the formation of the world's vast deposits of heavy oil, which far exceed conventional oil assets such as those found in the Middle East. Methanogenic degradation is also a potentially important component of attenuation in hydrocarbon contamination plumes. Studies of the organisms, syntrophic partnerships, mechanisms, and geochemical signatures associated with methanogenic hydrocarbon degradation have identified common themes and diagnostic markers for this process in the subsurface. These studies have also identified the potential to engineer methanogenic processes to enhance the recovery of energy assets as biogenic methane from residual oils stranded in petroleum systems.

  2. Cultivation-dependent and cultivation-independent characterisation of hydrocarbon-degrading bacteria in Guaymas Basin sediments

    Directory of Open Access Journals (Sweden)

    Tony eGutierrez

    2015-07-01

    Full Text Available Marine hydrocarbon-degrading bacteria perform a fundamental role in the biodegradation of crude oil and its petrochemical derivatives in coastal and open ocean environments. However, there is a paucity of knowledge on the diversity and function of these organisms in deep-sea sediment. Here we used stable-isotope probing (SIP, a valuable tool to link the phylogeny and function of targeted microbial groups, to investigate polycyclic aromatic hydrocarbon (PAH-degrading bacteria under aerobic conditions in sediments from Guaymas Basin with uniformly labeled [13C]phenanthrene. The dominant sequences in clone libraries constructed from 13C-enriched bacterial DNA (from phenanthrene enrichments were identified to belong to the genus Cycloclasticus. We used quantitative PCR primers targeting the 16S rRNA gene of the SIP-identified Cycloclasticus to determine their abundance in sediment incubations amended with unlabeled phenanthrene and showed substantial increases in gene abundance during the experiments. We also isolated a strain, BG-2, representing the SIP-identified Cycloclasticus sequence (99.9% 16S rRNA gene sequence identity, and used this strain to provide direct evidence of phenanthrene degradation and mineralization. In addition, we isolated Halomonas, Thalassospira and Lutibacterium spp. with demonstrable phenanthrene-degrading capacity from Guaymas Basin sediment. This study demonstrates the value of coupling SIP with cultivation methods to identify and expand on the known diversity of PAH-degrading bacteria in the deep-sea.

  3. Cultivation-dependent and cultivation-independent characterization of hydrocarbon-degrading bacteria in Guaymas Basin sediments.

    Science.gov (United States)

    Gutierrez, Tony; Biddle, Jennifer F; Teske, Andreas; Aitken, Michael D

    2015-01-01

    Marine hydrocarbon-degrading bacteria perform a fundamental role in the biodegradation of crude oil and its petrochemical derivatives in coastal and open ocean environments. However, there is a paucity of knowledge on the diversity and function of these organisms in deep-sea sediment. Here we used stable-isotope probing (SIP), a valuable tool to link the phylogeny and function of targeted microbial groups, to investigate polycyclic aromatic hydrocarbon (PAH)-degrading bacteria under aerobic conditions in sediments from Guaymas Basin with uniformly labeled [(13)C]-phenanthrene (PHE). The dominant sequences in clone libraries constructed from (13)C-enriched bacterial DNA (from PHE enrichments) were identified to belong to the genus Cycloclasticus. We used quantitative PCR primers targeting the 16S rRNA gene of the SIP-identified Cycloclasticus to determine their abundance in sediment incubations amended with unlabeled PHE and showed substantial increases in gene abundance during the experiments. We also isolated a strain, BG-2, representing the SIP-identified Cycloclasticus sequence (99.9% 16S rRNA gene sequence identity), and used this strain to provide direct evidence of PHE degradation and mineralization. In addition, we isolated Halomonas, Thalassospira, and Lutibacterium sp. with demonstrable PHE-degrading capacity from Guaymas Basin sediment. This study demonstrates the value of coupling SIP with cultivation methods to identify and expand on the known diversity of PAH-degrading bacteria in the deep-sea. PMID:26217326

  4. Removal of polycyclic aromatic hydrocarbons from aqueous solution using plant residue materials as a biosorbent

    Energy Technology Data Exchange (ETDEWEB)

    Chen Baoliang, E-mail: blchen@zju.edu.cn [Department of Environmental Science, Zhejiang University, Hangzhou, Zhejiang 310028 (China); Zhejiang Provincial Key Laboratory of Organic Pollution Process and Control, Zhejiang University, Hangzhou, Zhejiang 310028 (China); Yuan Miaoxin; Liu Hao [Department of Environmental Science, Zhejiang University, Hangzhou, Zhejiang 310028 (China); Zhejiang Provincial Key Laboratory of Organic Pollution Process and Control, Zhejiang University, Hangzhou, Zhejiang 310028 (China)

    2011-04-15

    Graphical abstract: The structure-effect relationship provides a reference to select and modify plant residues as a biosorbent with high efficiency to tackle organic pollutants. Research highlights: {yields} Polycyclic aromatic hydrocarbons are effectively removed by plant residues. {yields} Biosorption mechanism of plant residues to abate PAHs is a partitioning process. {yields} Partition coefficients are negatively related with sugar contents of biosorbent. {yields} The aromatic component and K{sub ow} exhibit positive effects on biosorption. {yields} The structure-effect relationship guides plant residue using as a biosorbent. - Abstract: To elucidate biosorption mechanism and removal efficiency of plant residues as a biosorbent to abate polycyclic aromatic hydrocarbons (PAHs) in wastewater, sorption of PAHs onto wood chips (WC), ryegrass roots (RR), orange peels (OP), bamboo leaves (BL), and pine needles (PN) were investigated. The structural characterization of the biosorbents was analyzed by elemental composition, BET-N{sub 2} surface area, and Fourier transform infrared spectroscopy. PAHs sorption to the selected biosorbents were compared and correlated with their structures. Biosorption isotherms fit well with Freundlich equation and the mechanism was dominated by partition process. The magnitude of phenanthrene partition coefficients (K{sub d}) followed the order of PN > BL > OP > RR > WC, ranged from 2484 {+-} 24.24 to 5306 {+-} 92.49 L/kg. Except the WC sample, the K{sub d} values were negatively correlated with sugar content, polar index [(N + O)/C] of the biosorbents, while the aromatic component exhibited positive effects. For a given biosorbent of bamboo leaves, the carbon-normalized partition coefficients (K{sub oc}) were linearly correlated with octanol-water partition coefficients (K{sub ow}) of PAHs, i.e., log K{sub oc} = 1.16 log K{sub ow} - 1.21. The structure-effect relationship provides a reference to select and modify plant residues as a

  5. Interstellar polycyclic aromatic hydrocarbons and carbon in interplanetary dust particles and meteorites

    Science.gov (United States)

    Allamandola, L. J.; Sandford, S. A.; Wopenka, B.

    1987-01-01

    Raman spectra of interplanetary dust particles (IDPs) and meteorites containing material similar to polycyclic aromatic hydrocarbons (PAHs) show features that are similar in position and relative strength to interstellar IR emission features attributable to vibrational transitions in free molecular-sized PAHs. In addition, these spectra sometimes show red photoluminescence that has elsewhere been attributed to PAHs, and a part of the carbonaceous phase in IDPs and meteorites contain a degree of deuterium enrichment anticipated in small, free PAHs that are exposed to ISM UV radiation. These observations suggest that some of the IDPs' carbonaceous material may have been produced in circumstellar dust shells, and only slightly modified in interstellar space.

  6. Assessment of concentration, bioaccumulation and sources of polycyclic aromatic hydrocarbons in zooplankton of Chabahar Bay.

    Science.gov (United States)

    Ziyaadini, Morteza; Mehdinia, Ali; Khaleghi, Leila; Nassiri, Mahmoud

    2016-06-15

    The amounts and sources of polycyclic aromatic hydrocarbons (PAHs) and their bioaccumulation factors (BAFs) in the zooplankton community of Chabahar Bay were investigated. The highest amounts of total PAHs (tPAHs) in the water and zooplankton samples were 62.2ngL(-1) and 1478.6ngg(-1) dry weights, in near the Shahid Beheshti Port and desalination, respectively. The greatest amount of BAF (51,780) was obtained in the entry of Bay, and it was related to the phenanthrene accumulation. Using molecular ratio, the results showed that the major input source of PAH compounds in zooplankton of Chabahar Bay was pyrolytic (fuel) source. PMID:26944700

  7. Occurrence and sources of particulate nitro-polycyclic aromatic hydrocarbons in ambient air in Denmark

    DEFF Research Database (Denmark)

    Feilberg, A.; Poulsen, M.W.B.; Nielsen, T.;

    2001-01-01

    The occurrence of selected nitro-polycyclic aromatic hydrocarbons (nitro-PAHs) associated with atmospheric particulate matter has been investigated at an urban site and at a semi-rural site. For this purpose an analysis method based on gas chromatography and tandem ion trap mass spectrometry has...... been developed and applied. The nitro-PAK levels have been compared with levels of other air pollutants including unsubstituted PAHs, inorganic gases and particulate matter, as well as with meteorological parameters. Correlations and concentration ratios suggest that the dominant source of 9...

  8. Exposures to Particulate Matter and Polycyclic Aromatic Hydrocarbons and Oxidative Stress in Schoolchildren

    OpenAIRE

    Bae, Sanghyuk; Pan, Xiao-Chuan; Kim, Su-Young; Park, Kwangsik; Kim, Yoon-Hee; Kim, Ho; Hong, Yun-Chul

    2009-01-01

    Background Air pollution is known to contribute to respiratory and cardiovascular mortality and morbidity. Oxidative stress has been suggested as one of the main mechanisms for these effects on health. Objective The aim of this study was to analyze the effects of exposure to particulate matter (PM) with aerodynamic diameters ≤ 10 μm (PM10) and ≤ 2.5 μm (PM2.5) and polycyclic aromatic hydrocarbons (PAHs) on urinary malondialdehyde (MDA) levels in schoolchildren. Methods The study population co...

  9. Polycyclic aromatic hydrocarbons fingerprints in the Pichavaram mangrove-estuarine sediments, southeastern India

    OpenAIRE

    Ranjan, Rajesh Kumar; Routh, Joyanto; Ramanathan, A.L.; Klump, J. Val

    2012-01-01

    The sources and historical deposition of 16 polycyclic aromatic hydrocarbons (PAHs) were investigated in dated sediment cores from the Pichavaram mangrove–estuarine complex. The ΣPAH flux in mangrove and estuarine sediments was 0.064 ± 0.031 μg/cm2/yr and 0.043 ± 0.020 μg/cm2/yr, respectively. The PAH flux in sediments increased up-core, coinciding with rapid urbanization since the 1970s. The flux showed a decrease in recent years (since 1990), coinciding with less riverine discharge, and per...

  10. Structures and electronic properties of thin-films of polycyclic aromatic hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Natsume, Yutaka [Asahi-Kasei Corporation, 2-1 Samejima, Fuji, Shizuoka (Japan)], E-mail: natsume.yc@om.asahi-kasei.co.jp; Minakata, Takashi; Aoyagi, Takeshi [Asahi-Kasei Corporation, 2-1 Samejima, Fuji, Shizuoka (Japan)

    2009-03-02

    We report the fabrication and characterization of organic thin-film transistors (TFTs) using several polycyclic aromatic hydrocarbons (PAHs). Pentacene, ovalene, dibenzocoronene and hexabenzocoronene were deposited as organic semiconductors on silicon wafers with gold electrodes as the bottom-contact configuration of the TFTs. The pentacene TFT showed the highest field-effect mobility of more than 0.1 cm{sup 2}/Vs in comparison with the other PAHs. The results clarified that the high field-effect mobility of the pentacene thin film is due to large grain size and intrinsic electronic properties.

  11. Polycyclic aromatic hydrocarbons and the Oak Ridge National Laboratory's experimental coal program: minimizing the hazards

    Energy Technology Data Exchange (ETDEWEB)

    Forrester, R.C. III; Cochran, H.D.; Bolton, N.E.

    1977-01-01

    Many processing techniques for the liquefaction or gasification of coal are being developed at the Oak Ridge National Laboratory and elsewhere. Although different in many other respects, all coal conversion processes produce a liquid effluent comprising a complex mixture of hydrocarbons. Such mixtures invariably contain significant amounts of polycyclic, aromatic compounds, some of which are known to be highly active carcinogens. The underlying philosophy that has been adopted for the protection of personnel involved in experimental coal processing operations is defined, and procedures that have been instituted to govern the conduct of such experimental work and handling of associated coal-derived liquids are detailed.

  12. Polycyclic aromatic hydrocarbons (PAH) and polychlorinated biphenyls (PCB) in urban soils of Greater London, UK

    OpenAIRE

    Vane, Christopher H.; Kim, Alexander W.; Beriro, Darren J.; Cave, Mark R.; Knights, Katherine; Moss-Hayes, Vicky; Nathanail, Paul C.

    2014-01-01

    Surface soils from a 19 km2 area in east London, UK were analysed for polycyclic aromatic hydrocarbons (PAH) and polychlorinated biphenyls (PCB) (n = 76). ∑16 PAH ranged from 4 to 67 mg/kg (mean, 18 mg/kg) and ∑50 PAH ranged from 6 to 88 mg/kg (mean, 25 mg/kg). ∑7 PCB ranged from 1 to 750 μg/kg (mean, 22 μg/kg) and ∑tri-hepta PCB ranged 9 to 2600 μg/kg (mean, 120 μg/kg). Compared to other international cities concentrations were similar for PAH but higher for PCB. Normal background concentrat...

  13. Contamination of soils in the urbanized areas of Belarus with polycyclic aromatic hydrocarbons

    Science.gov (United States)

    Kukharchyk, T. I.; Khomich, V. S.; Kakareka, S. V.; Kurman, P. V.; Kozyrenko, M. I.

    2013-02-01

    The content of polycyclic aromatic hydrocarbons (PAHs) in the soils of urbanized areas, including the impact zones of Belarus, were studied. The concentrations of 16 PAHs in the soils were determined for individual and high-rise building zones, forests, and forest parks of Belarus. The levels of the PAH accumulation in the soils of different industrial enterprises and boiler stations were analyzed. Possible sources of soil contamination with PAHs were considered, and the structure of the PAHs in the soils was shown. The levels of the soil contamination were determined from the regulated parameters for individual compounds and the sum of 16 PAHs.

  14. Aromatic hydrocarbon pathology in fish following a large spill into the Nemadji River, Wisconsin, USA

    Science.gov (United States)

    Caldwell, C.A.

    1997-01-01

    On June 30, 1992, a train accident resulted in a rail car releasing 114,000 L of a complex mixture of aromatic hydrocarbons into the Nemadji River, a tributary of Lake Superior near Superior, Wisconsin (Table 1). Although the majority of the spilled material evaporated, damage to aquatic life was extensive. Several thousand fishes were killed and an inestimable number were exposed to low concentrations (kidney were examined for histopathology. Blood was collected to determine the severity of liver damage reflected by the presence of the serum enzymes (aspartate aminotransferase, alanine aminotransferase, and d - glutamyl transferase).

  15. A review on polycyclic aromatic hydrocarbons: Source, environmental impact, effect on human health and

    Directory of Open Access Journals (Sweden)

    Hussein I. Abdel-Shafy

    2016-03-01

    The aim of this review is to discuss PAHs impact on the environmental and the magnitude of the human health risks posed by such substances. They also contain important information on concentrations, burdens and fate of polycyclic aromatic hydrocarbons (PAHs in the atmosphere. The main anthropogenic sources of PAHs and their effect on the concentrations of these compounds in air are discussed. The fate of PAHs in the air, their persistence and the main mechanisms of their losses are presented. Health hazards associated with PAH air pollution are stressed.

  16. Humoral immunosuppression in men exposed to polycyclic aromatic hydrocarbons and related carcinogens in polluted environments.

    OpenAIRE

    Szczeklik, A; Szczeklik, J; Galuszka, Z; Musial, J; Kolarzyk, E; Targosz, D

    1994-01-01

    We evaluated humoral immunity by measuring IgG, IgA, IgM, and IgE concentrations in 274 male workers in an iron foundry in Cracow, Poland. There were two groups: 199 coke oven workers and 76 cold-rolling mill workers. The groups were similar with respect to age, length of work (average 15 years), and smoking habits. Exposure to polycyclic aromatic hydrocarbons (PAHs), assessed by personal and area monitoring, ranged from 0.2 to 50 micrograms/m3 benzo[a]pyrene in coke plant workers and was of ...

  17. Characterization and source apportionment of polycyclic aromatic hydrocarbons (PAHs) in Sediments from the Bohai Sea, China

    Science.gov (United States)

    Liu, Jihua; Hu, Ningjing; Shi, Xuefa

    2015-04-01

    Characterization and source apportionment of polycyclic aromatic hydrocarbons (PAHs) in Sediments from the Bohai Sea, China Liu Jihua, Hu Ningjing, Shi Xuefa First Institute of Oceanography, State Oceanic Administration, Qingdao 266061, China Polycyclic aromatic hydrocarbons (PAHs) are a class of ubiquitous organic contaminants in the environment. Indeed, 16 PAH compounds have been listed as priority pollutants by the United States Environmental Protection Agency and the European Union because of their potential toxicity to humans and ecosystems. As POPs are released or escape into the environment, their global accumulation in marine sediments generates a complex balance between inputs and outputs. Furthermore, PAHs in coastal sediments can serve as effective tracers of materials transport from land-to-sea (Fang et al., 2009). Hence, investigations of PAHs in sediments can provide useful information for further understanding of environmental processes and material transport. In this study, sixteen polycyclic aromatic hydrocarbons (PAHs) were extracted from a total of 112 surface sediment samples collected across the entire territory of the Bohai Sea. The detectable concentrations of PAHs ranged from 97.2 to 300.7 ng/g across all samples, indicating low contamination levels of PAHs compared with reported values for other coastal sediments in China and developed countries. The highest concentrations were found within three belts in the vicinity of Luan River Estuary-Qinhuangdao Harbor, the Cao River Estuary-Bohai Sea Center, and north of the Yellow River Estuary. The distribution patterns of PAHs and source identification implied that PAH contamination in the Bohai Sea mainly originates from offshore oil exploration, sewage discharge from rivers and shipping activities. Further Principal components analysis (PCA)/multivariate linear regression (MLR) analysis suggested that the contributions of spilled oil products (petrogenic), coal combustion and traffic

  18. Oxygen-containing polycyclic aromatic hydrocarbons (OPAHs) and their parent-PAHs in soil

    OpenAIRE

    Bandowe, Benjamin Acham Musa

    2010-01-01

    In spite of the higher toxicity of oxygen-containing polycyclic aromatic hydrocarbons (OPAHs) than of their parent-PAHs, there are only a few studies of the concentrations, composition pattern, sources and fate of OPAHs in soil, the presumably major environmental sink of OPAHs. This is related to the fact that there are only few available methods to measure OPAHs together with PAHs in soil. rnThe objectives of my thesis were to (i) develop a GC/MS-based method to measure OPAHs and their paren...

  19. Distribution and Risk Assessment of Polycyclic Aromatic Hydrocarbons in Vegetables Grown in Pakistan

    OpenAIRE

    Ashraf, Mohammad W.; Syed Iqleem H. Taqvi; Solangi, Amber R.; Qureshi, Umair A.

    2013-01-01

    Distribution and risk assessment of eight priority polycyclic aromatic hydrocarbons (PAHs) contents have been examined in different varieties of vegetables grown in Pakistan. The results showed that the total PAH contents were higher for root vegetables like potato and carrot (~13 μg/kg) and relatively lower for turnip (10.9 μg/kg), respectively while for the fruit vegetables, all the peels were found to be more contaminated than cores. The ratio of total PAH concentrations in peels with resp...

  20. Dermal uptake of polycyclic aromatic hydrocarbons after hairwash with coal-tar shampoo

    Energy Technology Data Exchange (ETDEWEB)

    Schooten, F.-J. van; Moonen, E.J.C.; Rhijnsburger, E.; Agen, B. van; Thijssen, H.H.W.; Kleinjans, J.C.S. [University of Limburg, Maastricht (Netherlands). Dept. of Health Risk Analysis and Toxicology

    1994-11-26

    Describes an experiment to assess the dermal uptake of polycyclic aromatic hydrocarbons (PAHs) after hairwashing with coal tar antidandruff shampoo. The urinary excretion of 1-hydroxypyrene (1-OH-P), a PAH metabolile was used to assess internal dose of PAH. A single use of coal tar shampoo resulted in increased 1-OH-P excretion in all members of the experimental group compared with the control group using a non-coal tar antidandruff shampoo. It is suggested that repeated use of coal tar shampoo would result in a high internal dose of carcinogenic PAH. 5 refs., 1 fig.

  1. Characteristics of wintertime polycyclic aromatic hydrocarbon assemblage in aerosol of the Southern Adriatic

    Science.gov (United States)

    Jovanović, V. Ž.; Pfendt, P. A.; Filipović, A. J.

    2007-09-01

    Features of polycyclic aromatic hydrocarbon (PAH) assemblage in aerosol samples collected from the atmosphere of Herceg Novi during the winter months of two successive years were studied. The results showed almost the same concentration profiles of identified PAHs for samples from the two periods analyzed, generally suggesting a similar origin. Diagnostic ratios indicated combustion of wood and coal, emissions from petrol and diesel engines, and dust resuspension as sources that predominantly contributed to the atmospheric PAH concentrations. Statistical analysis, principal component analysis (PCA) in particular, allowed us to identify the impact of meteorological parameters on PAH abundance.

  2. Determination of basic azaarenes and polynuclear aromatic hydrocarbons in airborne particulate matter by gas chromatography

    DEFF Research Database (Denmark)

    Nielsen, Torben; Clausen, Peraxel; Jensen, Finn Palmgren

    1986-01-01

    phase (adjusted to pH 14 with potassium hydroxide) with dichloromethane, and determined by capillary gas chromatography (g.c.) with a nitrogen-sensitive detector. The PAH in the toluene phase are isolated by means of semipreparative high-performance liquid chromatography and liquid-liquid extraction......Polynuclear aromatic hydrocarbons (PAH) and their nitrogen analogs, basic azaarenes, are extracted from samples of airborne particulate matter by toluene with ultrasonic treatment. The basic azaarenes are extracted from the toluene phase with phosphoric acid, re-extracted from the phosphoric acid...

  3. A DFT-based toxicity QSAR study of aromatic hydrocarbons to Vibrio fischeri: Consideration of aqueous freely dissolved concentration.

    Science.gov (United States)

    Wang, Ying; Yang, Xianhai; Wang, Juying; Cong, Yi; Mu, Jingli; Jin, Fei

    2016-05-01

    In the present study, quantitative structure-activity relationship (QSAR) techniques based on toxicity mechanism and density functional theory (DFT) descriptors were adopted to develop predictive models for the toxicity of alkylated and parent aromatic hydrocarbons to Vibrio fischeri. The acute toxicity data of 17 aromatic hydrocarbons from both literature and our experimental results were used to construct QSAR models by partial least squares (PLS) analysis. With consideration of the toxicity process, the partition of aromatic hydrocarbons between water phase and lipid phase and their interaction with the target biomolecule, the optimal QSAR model was obtained by introducing aqueous freely dissolved concentration. The high statistical values of R(2) (0.956) and Q(CUM)(2) (0.942) indicated that the model has good goodness-of-fit, robustness and internal predictive power. The average molecular polarizability (α) and several selected thermodynamic parameters reflecting the intermolecular interactions played important roles in the partition of aromatic hydrocarbons between the water phase and biomembrane. Energy of the highest occupied molecular orbital (E(HOMO)) was the most influential descriptor which dominated the toxicity of aromatic hydrocarbons through the electron-transfer reaction with biomolecules. The results demonstrated that the adoption of freely dissolved concentration instead of nominal concentration was a beneficial attempt for toxicity QSAR modeling of hydrophobic organic chemicals. PMID:26812082

  4. Limitations of microbial hydrocarbon degradation at the Amon mud volcano (Nile deep-sea fan

    Directory of Open Access Journals (Sweden)

    J. Felden

    2013-05-01

    Full Text Available The Amon mud volcano (MV, located at 1250 m water depth on the Nile deep-sea fan, is known for its active emission of methane and non-methane hydrocarbons into the hydrosphere. Previous investigations showed a low efficiency of hydrocarbon-degrading anaerobic microbial communities inhabiting the Amon MV center in the presence of sulfate and hydrocarbons in the seeping subsurface fluids. By comparing spatial and temporal patterns of in situ biogeochemical fluxes, temperature gradients, pore water composition, and microbial activities over 3 yr, we investigated why the activity of anaerobic hydrocarbon degraders can be low despite high energy supplies. We found that the central dome of the Amon MV, as well as a lateral mud flow at its base, showed signs of recent exposure of hot subsurface muds lacking active hydrocarbon degrading communities. In these highly disturbed areas, anaerobic degradation of methane was less than 2% of the methane flux. Rather high oxygen consumption rates compared to low sulfide production suggest a faster development of more rapidly growing aerobic hydrocarbon degraders in highly disturbed areas. In contrast, the more stabilized muds surrounding the central gas and fluid conduits hosted active anaerobic hydrocarbon-degrading microbial communities. The low microbial activity in the hydrocarbon-vented areas of Amon MV is thus a consequence of kinetic limitations by heat and mud expulsion, whereas most of the outer MV area is limited by hydrocarbon transport.

  5. Utilizing carbon dioxide as a reaction medium to mitigate production of polycyclic aromatic hydrocarbons from the thermal decomposition of styrene butadiene rubber.

    Science.gov (United States)

    Kwon, Eilhann E; Yi, Haakrho; Castaldi, Marco J

    2012-10-01

    The CO(2) cofeed impact on the pyrolysis of styrene butadiene rubber (SBR) was investigated using thermogravimetric analysis (TGA) coupled to online gas chromatography/mass spectroscopy (GC/MS). The direct comparison of the chemical species evolved from the thermal degradation of SBR in N(2) and CO(2) led to a preliminary mechanistic understanding of the formation and relationship of light hydrocarbons (C(1-4)), aromatic derivatives, and polycyclic aromatic hydrocarbons (PAHs), clarifying the role of CO(2) in the thermal degradation of SBR. The identification and quantification of over 50 major and minor chemical species from hydrogen and benzo[ghi]perylene were carried out experimentally in the temperature regime between 300 and 500 °C in N(2) and CO(2). The significant amounts of benzene derivatives from the direct bond dissociation of the backbone of SBR, induced by thermal degradation, provided favorable conditions for PAHs by the gas-phase addition reaction at a relatively low temperature compared to that with conventional fuels such as coal and petroleum-derived fuels. However, the formation of PAHs in a CO(2) atmosphere was decreased considerably (i.e., ∼50%) by the enhanced thermal cracking behavior, and the ultimate fates of these species were determined by different pathways in CO(2) and N(2) atmospheres. Consequently, this work has provided a new approach to mitigate PAHs by utilizing CO(2) as a reaction medium in thermochemical processes. PMID:22950720

  6. Distribution and fate of aliphatic and aromatic hydrocarbons in Antarctic fauna and environment

    Science.gov (United States)

    Platt, H. M.; Mackie, P. R.

    1980-03-01

    With the depletion of oil resources in more accessible areas, those of remote regions are being considered or indeed are now being exploited. In many of these regions, especially the polar ones, little is known of the effects such exploitation will have on the environment. But it is known that the ecosystems are often subject to great stress by natural climatic conditions and additional burdens imposed by man may have catastrophic environmental effects. South Georgia, a sub-Antarctic island, has a history of industrial activity mainly concerned with whaling operations that peaked around 1925-1935 but has since declined to virtually nothing. Studies of the ecology of the area provided a unique opportunity to assess the long-term effects that such activities had on the ecosystem. Off the whaling stations a considerable amount of waste material, including fuel oil, was released into the bays and inevitably some of this material was deposited in the sediments. Chemical evidence in the form of both paraffinic and aromatic hydrocarbons still persists in the sediments. The implications of this persistence in relation to the possible influence of the low temperature conditions are discussed. The superficial sediments, marine biota and terrestrial plants, which since 1965 have returned virtually to a pristine state, contain hydrocarbons essentially similar to unpolluted areas around the coast of Britain. Relatively high levels of carcinogenic/mutagenic polynuclear aromatic hydrocarbons in surface sediments suggests a world-wide background of abiogenic hydrocarbons probably disseminated by airborne transport. This appears to indicate that contamination reaches even remote parts of the world in relatively undiminished quantities.

  7. Trichloroethylene metabolism by microorganisms that degrade aromatic compounds.

    OpenAIRE

    1988-01-01

    Trichloroethylene (TCE) was metabolized by the natural microflora of three different environmental water samples when stimulated by the addition of either toluene or phenol. Two different strains of Pseudomonas putida that degrade toluene by a pathway containing a toluene dioxygenase also metabolized TCE. A mutant of one of these strains lacking an active toluene dioxygenase could not degrade TCE, but spontaneous revertants for toluene degradation also regained TCE-degradative ability. The re...

  8. Analysis of aromatic hydrocarbons in overburden from coal mines: Assessment of the environmental impact

    International Nuclear Information System (INIS)

    Bituminous coals are known to contain significant amounts of petroleum-like hydrocarbons trapped in the pore system of the macromolecular network. With increasing thermal stress acting upon coals under the particular conditions in their deposits, the relative amount of volatile aromatic hydrocarbons within the trapped bitumen increases until the coal reaches the rank of medium-volatile bituminous coals. Coking coals particularly are rich in compounds such as benzene, biphenyl, naphthalene, and their alkylated derivatives. Potential hazardous environmental impact of these hydrocarbons has to be considered when mining or reclaiming overburden because approximately 10% overburden material related to coal mining is coal. Exposure to long-term weathering destroys the pore system of coals, which might result in a release of highly volatile bituminous coal constituents into the atmosphere. This view is supported by analyses of coals present in overburden material. In the present study, the on-line combination of thermodesorption coupled to gas chromatography and mass spectrometry is shown to be an appropriate tool for the detection and quantitation of hydrocarbons of a wide boiling temperature range present in solid sample material. The method is preferentially suitable for the analysis of highly volatile constituents such as benzene, toluene, and xylenes, which are not quantitatively analyzed using conventional solvent-extraction methods

  9. Degradation of Chlorinated Aromatic Compounds in UASB Reactors

    DEFF Research Database (Denmark)

    Christiansen, Nina; Hendriksen, Hanne Vang; Järvinen, Kimmo T.;

    1995-01-01

    Data on anaerobic degradation of chloroaromatic compounds in Upflow Anaerobic Sludge Blanket Reactors (UASB-reactor) are presented and compared. Special attention is given to the metabolic pathways for degradation of chlorinated phenols by granular sludge. Results indicate that PCP can be degraded...

  10. Oil and gas potential assessment for coal measure source rocks on absolute concentration of n-alkanes and aromatic hydrocarbons

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    Absolute concentration of normal alkanes(n-alkanes) and aromatic hydrocarbons in bitumen extracted from source rocks in the period of thermodegradation from Turpan-Hami Basin suggests that aromatic hydrocarbons are dominant in coal and carbargilite while n-alkanes are dominant in mudstones. Bulkrock analysis and gas chromatograph/mass spectrum(GC-MS) of source rocks shows aromatic hydrocarbons are dominant in total ion chromatograms(TIC) of samples with poor perhydrous macerals while n-alkanes are dominant in TICs of samples with abundant perhydrous macerals. The identification of oil-prone and gas prone property based on GC-MS of bitumen "A" together with bulkrock analysis indicates that source rocks from Shengbei area are more oil-prone while source rocks from Qiudong and Xiaocaohu areas are more gas-prone,coinciding with the distribution of oil and gas reservoirs in Taibei Sag. Ratios used to identify oil-prone and gas-prone property for source rocks from Turpan Basin are proposed:n-alkanes >110 μg·mg-1,aromatics <15 μg·mg-1,and n-alkanes/aromatics >8 for oil-prone source rock bitumen while n-alkanes<82 μg·mg-1,aromatics >40 μg·mg-1,and n-alkanes/aromatics <1.5 for gas-prone source rock bitumen.

  11. Aromatic compound degradation by iron reducing bacteria isolated from irrigated tropical paddy soils

    Institute of Scientific and Technical Information of China (English)

    LU Wenjing; WANG Hongtao; HUANG Changyong; W. Reichardt

    2008-01-01

    Forty-six candidate phenol/benzoate degrading-iron reducing bacteria were isolated from long term irrigated tropical paddy soils by enrichment procedures. Pure cultures and some prepared mixed cultures were examined for ferric oxide reduction and phenol/benzoate degradation. All the isolates were iron reducers, but only 56.5% could couple iron reduction to phenol and/or benzoate degradation, as evidenced by depletion of phenol and benzoate after one week incubation. Analysis of degradative capability using Biolog MT plates revealed that most of them could degrade other aromatic compounds such as ferulic acid, vanillic acid, and hydroxybenzoate. Mixed-cultures and soft samples displayed greater capacity for aromatic degradation and iron reduction than pure bacterial isolates, suggesting that these reactions may be coupled via a consortia-based mechanism in paddy soils.

  12. Life in oil :Hydrocarbon-degrading bacterial mineralization in oil spill-polluted marine environment

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    play the greatest role under neutral to alkaline condition (pH;7-7.8).On the contrary,when pH shifted to acidic (pH;2-4) levels,the fungi took over to degrade heavy oil.During the period,the aliphatic hydrocarbons were reduced significantly but the aromatic hydrocarbons remained relatively constant even after 429 days of bioremediation.Experimental study was undertaken to investigate the bioavailability of kaolinite clay minerals and the role they play in seawater polluted with the Nakhodka oil spill.TEM/EDS imaging suggested that the clays present in oil-polluted seawater were capable of stimulating oildegrading bacteria probably because Si from clays facilitates bacterial usage of oil and C-O-Na-Si complexes on the surfaces of bacterial cell walls are a stimulator for oildegrading bacterial growth in seawater contaminated with the Nakhodka oil spill.

  13. Aliphatic and polycyclic aromatic hydrocarbons in sediments of the Slovenian coastal area (Gulf of Trieste, northern Adriatic).

    Science.gov (United States)

    Bajt, Oliver

    2012-12-01

    The distribution and sources of aliphatic and polycyclic aromatic hydrocarbons (PAH) were determined in sediments at seven sites around the Slovenian coastal area. The potential toxicological significance was also assessed using biological thresholds. The results of the analyses showed higher concentrations of hydrocarbons in the Port of Koper and in the Marina of Portoroz. The influence of pollution was also evident in rather higher concentrations of hydrocarbons in the surrounding area in the Bays of Koper and Piran. Concentrations of hydrocarbons decrease toward the central part of the Gulf of Trieste. The major component of the aliphatic fraction was the unresolved complex mixture. Concentrations of the total resolved aliphatic hydrocarbons were in a range from 689 to 3,164 ng g(-1). Concentrations of the total PAHs were between 330 and 1,173 ng g(-1). Polycyclic aromatic hydrocarbons are primarily of pyrolytic origin with some smaller contributions of the petrogenic, while the aliphatic are mostly of petrogenic origin with significant amounts of biogenic derived compounds of terrestrial and marine origin. Strong evidence of the diagenetic origin of perylene in the investigated area was also found. Quite a good linear relationship between PAH concentration and TOC and between aliphatic hydrocarbon concentrations and TOC was observed. The principal component analysis showed differences between the nearshore and offshore sites. In general, the investigated area is moderately contaminated by hydrocarbons. Concentrations of PAHs, hydrocarbons of high concern, are below the levels (effects range low and the effects range median) associated with adverse biological effects. PMID:22270593

  14. Turn-On Fluorogenic and Chromogenic Detection of Small Aromatic Hydrocarbon Vapors by a Porous Supramolecular Host.

    Science.gov (United States)

    Hatanaka, Sou; Ono, Toshikazu; Hisaeda, Yoshiio

    2016-07-18

    Benzene, toluene, ethylbenzene, the isomers of xylene, and trimethylbenzene are harmful volatile organic compounds and pose risks to human health and the environment. However, there are currently no effective chemosensors for vapors of these compounds. A porous supramolecular host for turn-on fluorogenic and chromogenic detection of the vapors of small aromatic hydrocarbons is presented. The host was constructed from a naphthalenediimide derivative that was supramolecularly connected to tris(pentafluorophenyl)borane. The amorphous powder form of the host allowed for effective accommodation of vapors of small aromatic hydrocarbons, resulting in a guest-dependent fluorescence emission. Increases in the fluorescence yield of 76-, 46-, and 37-fold were observed with toluene, benzene, and m-xylene, respectively. Negligible responses were obtained with common organic solvents. This simple supramolecular host could be applied as a useful sensor of small aromatic hydrocarbon vapors. PMID:27224939

  15. Evaluation of methods for predicting the toxicity of polycyclic aromatic hydrocarbon mixtures

    Energy Technology Data Exchange (ETDEWEB)

    Reeves, W.; Barhoumi, R.; Burghardt, R.C. [and others] [Texas A & M University, College Station, TX (USA). Dept. of Veterinary Anatomy and Public Health and Department of Civil Engineering

    2001-04-15

    Risk assessments of polycyclic aromatic hydrocarbon mixtures are hindered by a lack of reliable information on the potency of both mixtures and their individual components. This paper examines methods for approximating the toxicity of polycyclic aromatic hydrocarbon (PAH) mixtures. PAHs were isolated from a coal tar and then separated by ring number using HPLC. Five fractions (A-E) were generated, each possessing a unique composition and expected potency. The toxicity of each fraction was measured in the Salmonella/mutagenicity assay and the Chick Embryo Screening Test (CHEST). Their abilities to induce ethoxyresorufin-O-deethylase and to inhibit gap junction intercellular communication in rat liver Clone 9 cells were also measured. In the Salmonella/mutagenicity assay, fractions were predicted to have potencies in the order C {gt} E {gt} B {gt} A. Toxic equivalency factors (TEFs) for fractions A-E were in the order E {ge} D {gt} C {gt} B {gt} A. TEF values were 20 652, 20 929, 441, 306 and 74.1 {mu}g of BaP equiv/g, respectively. A lack of agreement between assay-predicted potencies and chemical analysis-predicted potencies was observed with other assays and other methods of calculation. The results demonstrate the limitations of using a single method to predict the toxicity of a complex PAH mixture. 41 refs., 2 figs., 3 tabs.

  16. Polycyclic Aromatic Hydrocarbons (PAHs) in urban atmospheric particulate of NCR, Delhi, India

    Science.gov (United States)

    Sonwani, Saurabh; Amreen, Hassan; Khillare, P. S.

    2016-07-01

    The present study identifies the particulate Polycyclic Aromatic hydrocarbons (PAHs) and their sources in ambient atmosphere of Delhi, India. PM10 (aerodynamic diameter, ≤10 μm) samples were collected weekly at two residential areas from July 2013 to January 2014. First sampling site was located in centre of the city, while other was at city's background (located in South-East direction of the Delhi). PM10 was collected on Whatman GF/A (8"x10") glass fibre filters using High-Volume sampler having a constant flow rate of 1.10 m3/min. A total of 55 samples, 27 from city centre and 28 from background site were collected during sampling period, covering two different seasons. The samples were analysed for determination of 16 Polycyclic Aromatic Hydrocarbons by using High Performance Liquid Chromatography (HPLC) system (Waters, USA). A source apportionment study using Molecular Diagnostic Ratio (MDR) and Principal Component Analysis (PCA) were conducted for both sampling sites in order to identify the potential PAHs sources in Delhi. MDR was used for the preliminary identification of sources and PCA was used for further confirmation of the PAH sources at both the sites in Delhi. Results indicated towards traffic and coal combustion related sources as dominant contributors of urban atmospheric PAHs in Delhi.

  17. Combined effect of urinary monohydroxylated polycyclic aromatic hydrocarbons and impaired lung function on diabetes.

    Science.gov (United States)

    Hou, Jian; Sun, Huizhen; Xiao, Lili; Zhou, Yun; Yin, Wenjun; Xu, Tian; Cheng, Juan; Chen, Weihong; Yuan, Jing

    2016-07-01

    Associations of type 2 diabetes with exposure to polycyclic aromatic hydrocarbons and reduced lung function have been reported. The aim of the present study was to investigate effect of reduced lung function and exposure to background PAHs on diabetes. A total of 2730 individuals were drawn from the Wuhan-Zhuhai (WHZH) Cohort Study (n=3053). Participants completed physical examination, measurement of lung function and urinary monohydroxylated polycyclic aromatic hydrocarbons (OH-PAHs). Risk factors for type 2 diabetes were identified by multiple logistic regression analysis, and the presence of additive interaction between levels of urinary OH-PAHs and lower lung function was evaluated by calculation of the relative excess risk due to interaction (RERI) and attributable proportion due to interaction (AP). Urinary OH-PAHs levels was positively associated with type 2 diabetes among individuals with impaired lung function (pFEV1, odd ratio (OR): 0.664, 95% confidence interval (CI): 0.491-0.900) and forced vital capacity (FVC, OR: 0.693, 95% CI: 0.537-0.893) were negatively associated with diabetes among individuals. Additive interaction of higher urinary levels of OH-PAHs and lower FVC (RERI: 0.679, 95% CI: 0.120-1.238); AP: 0.427, 95% CI: 0.072-0.782) was associated with diabetes. Exposure to background PAHs was related to diabetes among individuals with lower lung function. Urinary levels of OH-PAHs and reduced lung function had an additive effect on diabetes. PMID:27136672

  18. Sequential accelerated solvent extraction of polycyclic aromatic hydrocarbons with different solvents: performance and implication.

    Science.gov (United States)

    Ma, Xiaoxuan; Ran, Yong; Gong, Jian; Chen, Diyun

    2010-01-01

    Sixteen USEPA priority polycyclic aromatic hydrocarbons (PAHs) extracted by Soxhlet extraction (S-PAHs) with dichloromethane and routine accelerated solvent extraction (A-PAHs) with 1:1 toluene/methanol, respectively, were investigated in 24 soil samples from two cities in the center of the Pearl River Delta, South China. Polycyclic aromatic hydrocarbons, methylphenanthrene and perylene, in two soils, two sediments, and an immature oil shale were also sequentially extracted by accelerated solvent extraction (ASE) with each of four different organic solvents for three times. The A-PAHs' concentrations are 2.41 times the S-PAHs' concentrations. For sequential three ASEs, PAHs in the first extract account for 56 to 67% of their total concentrations in the sequential three extractions and toluene displays the best extraction performance among the four solvents. Diagnostic ratios of PAHs in Soxhlet extraction, routine ASE, and sequential ASE with each solvent for a given sample are very similar, suggesting their identical petrogenic and pyrogenic sources in the soils and sediments. But the PAH ratios for the shale have an obvious petrogenic origin. The perylene/5-ring PAH ratios indicate a diagenetic source, especially in the shale and sediments. The correlation analysis shows that A-PAHs/S-PAHs is better associated with the contents of total organic carbon (TOC) than those of black carbon (BC). The above results indicate the significant petrogenic origin of PAHs and the important effect of organic matter on their extraction and distribution in the investigated field soils/sediments. PMID:21284305

  19. Brine-induced advection of dissolved aromatic hydrocarbons to arctic bottom waters

    International Nuclear Information System (INIS)

    Extruded brine, generated during sea ice formation in nearshore arctic waters, will sink to the bottom and can form a stable bottom boundary layer. This layer can persist for periods of up to 4-6 months. Limited quantities of dissolved aromatic hydrocarbons resulting from a spill of crude oil or refined petroleum distillate products during periods of ice growth can be transported as conservative components to the benthos with sinking brine. Once incorporated into the stable bottom boundary layer, these aromatic components are no longer subject to loss by evaporative processes, and they only can be diluted by ultimately mixing with uncontaminated water masses, a process that proceeds slowly throughout the ice-covered period. This mechanism for the transport of dissolved hydrocarbons has been demonstrated through a laboratory test-tank simulation and a chemical/physical oceanographic field program conducted in the Chukchi Sea near Pt. Frankline, AK (March 1985). The results are pertinent to shallow nearshore oil and gas exploration, development, production, and transportation activities in high latitude marine systems

  20. Assessment of atmospheric distribution of polychlorinated biphenyls and polycyclic aromatic hydrocarbons using polyparameter model

    Directory of Open Access Journals (Sweden)

    Turk-Sekulić Maja M.

    2011-01-01

    Full Text Available Results of partial or total destruction of industrial plants, military targets, infrastructure, uncontrolled fires and explosions during the conflict period from 1991 to 1999, at the area of Western Balkans, were large amounts of hazardous organic matter that have been generated and emitted in the environment. In order to assess gas/particle partition of seven EPA polychlorinated biphenyls and sixteen EPA polycyclic aromatic hydrocarbons, twenty air samples have been collected at six urban, industrial and highly contaminated localities in Vojvodina. Hi-Vol methodology has been used for collecting ambiental air samples, that simultaneously collects gaseous and particulate phase with polyurethane foam filters (PUF and glass fiber filters (GFF. PUF and GFF filters have been analyzed, and concentration levels of gaseous PCBs and PAHs molecules in gaseous and particulate phase were obtained, converted and expressed through fraction of individual compounds sorbed onto particulate phase of the sample, in total detected quantity. Experimentally gained gas/particle partitioning values of PCBs and PAHs molecules have been compared with PP-LFER model estimated values. Significant deviation has been noticed during comparative analysis of estimated polyparameter model values for complete set of seven PCBs congeners. Much better agreement of experimental and estimated values is for polycyclic aromatic hydrocarbons, especially for molecules with four rings. These results are in a good correlation with literature data where polyparameter model has been used for predicting gas/particle partition of studied group of organic molecules.

  1. Differential scanning calorimetry method for purity determination: A case study on polycyclic aromatic hydrocarbons and chloramphenicol

    Energy Technology Data Exchange (ETDEWEB)

    Kestens, V., E-mail: vikram.KESTENS@ec.europa.eu [European Commission - Joint Research Centre, Institute for Reference Materials and Measurements (IRMM), Retieseweg 111, 2440 Geel (Belgium); Zeleny, R.; Auclair, G.; Held, A.; Roebben, G.; Linsinger, T.P.J. [European Commission - Joint Research Centre, Institute for Reference Materials and Measurements (IRMM), Retieseweg 111, 2440 Geel (Belgium)

    2011-09-20

    Highlights: {yields} Purity assessment of polycyclic aromatic hydrocarbons and chloramphenicol by DSC. {yields} DSC results compared with traditional purity methods. {yields} Different methods give different results, multiple method approach recommended. {yields} DSC sensitive to impurities that have similar structures as main component. - Abstract: In this study the validity and suitability of differential scanning calorimetry (DSC) to determine the purity of selected polycyclic aromatic hydrocarbons and chloramphenicol has been investigated. The study materials were two candidate certified reference materials (CRMs), 6-methylchrysene and benzo[a]pyrene, and two different batches of commercially available highly pure chloramphenicol. The DSC results were compared with those obtained by other methods, namely gas and liquid chromatography with mass spectrometric detection, liquid chromatography with diode array detection, and quantitative nuclear magnetic resonance. The purity results obtained by these different analytical methods confirm the well-known challenges of comparing results of different method-defined measurands. In comparison with other methods, DSC has a much narrower working range. This limits the applicability of DSC as purity determination method, for instance during the assignment of the purity value of a CRM. Nevertheless, this study showed that DSC can be a powerful technique to detect impurities that are structurally very similar to the main purity component. From this point of view, and because of its good repeatability, DSC can be considered as a valuable technique to investigate the homogeneity and stability of candidate purity CRMs.

  2. Retention mechanism for polycyclic aromatic hydrocarbons in reversed-phase liquid chromatography with monomeric stationary phases.

    Science.gov (United States)

    Rafferty, Jake L; Siepmann, J Ilja; Schure, Mark R

    2011-12-23

    Reversed-phase liquid chromatography (RPLC) is the foremost technique for the separation of analytes that have very similar chemical functionalities, but differ only in their molecular shape. This ability is crucial in the analysis of various mixtures with environmental and biological importance including polycyclic aromatic hydrocarbons (PAHs) and steroids. A large amount of effort has been devoted to studying this phenomenon experimentally, but a detailed molecular-level description remains lacking. To provide some insight on the mechanism of shape selectivity in RPLC, particle-based simulations were carried out for stationary phases and chromatographic parameters that closely mimic those in an experimental study by Sentell and Dorsey [J. Chromatogr. 461 (1989) 193]. The retention of aromatic hydrocarbons ranging in size from benzene to the isomeric PAHs of the formula C(18)H(12) was examined for model RPLC systems consisting of monomeric dimethyl octadecylsilane (ODS) stationary phases with surface coverages ranging from 1.6 to 4.2 μmol/m(2) (i.e., stationary phases yielding low to intermediate shape selectivity) in contact with a 67/33 mol% acetonitrile/water mobile phase. The simulations show that the stationary phase acts as a very heterogeneous environment where analytes with different shapes prefer different spatial regions with specific local bonding environments of the ODS chains. However, these favorable retentive regions cannot be described as pre-existing cavities because the chain conformation in these local stationary phase regions adapts to accommodate the analytes.

  3. Questioning the existence of superconducting potassium doped phases for aromatic hydrocarbons

    Science.gov (United States)

    Heguri, Satoshi; Kobayashi, Mototada; Tanigaki, Katsumi

    2015-07-01

    Superconductivity in aromatic hydrocarbons doped with potassium (K) such as K3 [picene (PCN)] and K3 [phenanthrene (PHN)] is found for only armchair-type polycyclic aromatic hydrocarbon. In this paper the thermodynamics of the reaction processes of PHN or anthracene (AN, zigzag type) with K was studied using differential scanning calorimetry and x-ray diffraction. We show that PHN decomposes during the reaction, triggered by hydrogen abstraction, to give metal hydride KH and unknown amorphous. No stable doped phases exist in Kx(PHN ) with stoichiometries of x =1 -3 . However, in the case of AN, a stable doped phase forms. We claim that PHN, which has been reported to be energetically more stable in the ground state than AN by first principle calculations, is unstable upon doping. We also suggest that the superconductivity in K3(PCN ) is due to the misinterpretation of experimental data, which actually arises from ferromagnetic impurities. We have never detected the superconductivity above 2 K in these compounds. The superconductivity in both Kx(PHN ) and Kx(PCN ) is concluded to be highly questionable.

  4. Characteristics of polycyclic aromatic hydrocarbon emissions of particles of various sizes from smoldering incense.

    Science.gov (United States)

    Yang, T T; Lin, T S; Wu, J J; Jhuang, F J

    2012-02-01

    Release of polycyclic aromatic hydrocarbons (PAHs) in particles of various sizes from smoldering incenses was determined. Among the three types of incense investigated, yielding the total PAH emission rate and factor ranges for PM0.25 were 2,139.7-6,595.6 ng/h and 1,762.2-8,094.9 ng/g, respectively. The PM0.25/PM2.5 ratio of total PAH emission factors and rates from smoldering three incenses was greater than 0.92. This study shows that total particle PAH emission rates and factors were mainly incenses. The benzo[a]pyrene accounted for 65.2%-68.0% of the total toxic equivalency emission factor of PM2.5 for the three incenses. Experimental results clearly indicate that the PAH emission rates and factors were influenced significantly by incense composition, including carbon and hydrogen content. The study concludes that smoldering incense with low atomic hydrogen/carbon ratios minimized the production of total polycyclic aromatic hydrocarbons of both PM2.5 and PM0.25.

  5. Risk of human exposure to polycyclic aromatic hydrocarbons: A case study in Beijing, China

    International Nuclear Information System (INIS)

    Polycyclic aromatic hydrocarbons (PAHs) can cause adverse effects on human health. The relative contributions of their two major intake routes (diet and inhalation) to population PAH exposure are still unclear. We modeled the contributions of diet and inhalation to the overall PAH exposure of the population of Beijing in China, and assessed their human incremental lifetime cancer risks (ILCR) using a Mont Carlo simulation approach. The results showed that diet accounted for about 85% of low-molecular-weight PAH (L-PAH) exposure, while inhalation accounted for approximately 57% of high-molecular-weight PAH (H-PAH) exposure of the Beijing population. Meat and cereals were the main contributors to dietary PAH exposure. Both gaseous- and particulate-phase PAHs contributed to L-PAH exposure through inhalation, whereas exposure to H-PAHs was mostly from the particulate-phase. To reduce the cancer incidence of the Beijing population, more attention should be given to inhaled particulate-phase PAHs with considerable carcinogenic potential. - Highlights: • We modeled the contributions of diet and inhalation to population PAH exposure. • Diet contributed 85% of population exposure to low molecular-weight PAHs. • Inhalation contributed 57% of population exposure to high molecular-weight PAHs. • The PAH exposure level with body-weight adjustment decreased with age increasing. • The population cancer risk of PAH exposure is lower than the serious risk level. - The exposure of the Beijing population to carcinogenic polycyclic aromatic hydrocarbons was mainly from inhaled particulate matter

  6. Polycyclic aromatic hydrocarbons in Recent lake sediments—I. Compounds having anthropogenic origins

    Science.gov (United States)

    Wakeham, Stuart G.; Schaffner, Christian; Giger, Walter

    1980-03-01

    Polycyclic aromatic hydrocarbons (PAH) in sediment cores from Lake Lucerne, Lake Zürich, and Greifensee, Switzerland, and Lake Washington, northwest U.S.A., have been isolated, identified and quantified by glass capillary gas chromatography and gas chromatography/mass spectrometry. Surface sediment layers are greatly enriched in PAH—up to 40 times—compared to deeper layers. In addition, concentration increases in upper sediments generally correspond to increasing industrialization and urbanization in the catchment basins of the lakes. Few PAH could be detected in pre-industrial revolution sediments, indicating that background levels for most PAH in aquatic sediments are extremely low. These results are consistent with an anthropogenic source for most of the aromatic hydrocarbons present in the modern sediments. A comparison of PAH distributions in the sediments and in possible source materials shows that urban runoff of street dust may be the most important PAH input to these lacustrine sediments. There is evidence that a significant contribution to the PAH content of street dust comes from material associated with asphalt.

  7. City air pollution of polycyclic aromatic hydrocarbons and other mutagens: occurrence, sources and health effects

    DEFF Research Database (Denmark)

    Nielsen, T.; Ejsing Jørgensen, Hans; Larsen, J.C.;

    1996-01-01

    The presence of polycyclic aromatic hydrocarbons (PAH), mutagens and other air pollutants was investigated in a busy street in central Copenhagen and in a park area adjacent to the street. The winter concentration of benzo(a)pyrene was 4.4+/-1.2 ng/m(3) in the street air and 1.4+/-0.6 ng/m(3) in ...... was estimated to be 40%. Four different approaches to evaluate the health effects are discussed. The direct effect of PAH air pollution, and other mutagens, is considered to be a maximum of five lung cancer cases each year out of one million people.......The presence of polycyclic aromatic hydrocarbons (PAH), mutagens and other air pollutants was investigated in a busy street in central Copenhagen and in a park area adjacent to the street. The winter concentration of benzo(a)pyrene was 4.4+/-1.2 ng/m(3) in the street air and 1.4+/-0.6 ng/m(3...

  8. Contamination of Runoff Water at Gdańsk Airport (Poland) by Polycyclic Aromatic Hydrocarbons (PAHs) and Polychlorinated Biphenyls (PCBs)

    OpenAIRE

    Jacek Namieśnik; Anna Maria Sulej; Żaneta Polkowska

    2011-01-01

    Airport runoff can contain high concentrations of various pollutants, in particular polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs), the environmental levels of which have to be monitored. Airport runoff water samples, collected at the Gdańsk-Rębiechowo Airport from 2008 to 2009, were analysed for PAHs and PCBs by gas chromatography. The aromatic fractions were separated by liquid-liquid extraction and analysed by GC/MS. Total PAH concentrations were 295–6,758 ng/...

  9. Kekulé-based Valence Bond Model.Ⅱ. Diels-Alder Reactivity of Polycyclic Aromatic Hydrocarbons

    Institute of Scientific and Technical Information of China (English)

    MA,Jing(马晶); LI,Shu-Hua(黎书华); JIANG,Yuan-Sheng(江元生)

    2002-01-01

    The Kekule-based valence bond ( VB ) method was employed to study the ground state properties of 52 polycyclic aromatic hydrocarbons. The reactivity indices defined upon our VB calculations were demonstrated to be capable of quantitatively interpreting the secnd order rate constants of the Diels-Alder reactions. The qualitative trends of the reactivities of many homologous series can be also explained based on the local aromaticity index defined in this work.

  10. Isolation, identification, and crude oil degradation characteristics of a high-temperature, hydrocarbon-degrading strain.

    Science.gov (United States)

    Liu, Boqun; Ju, Meiting; Liu, Jinpeng; Wu, Wentao; Li, Xiaojing

    2016-05-15

    In this work, a hydrocarbon-degrading bacterium Y-1 isolated from petroleum contaminated soil in the Dagang Oilfield was investigated for its potential effect in biodegradation of crude oil. According to the analysis of 16S rRNA sequences, strain Y-1 was identified as Bacillus licheniformis. The growth parameters such as pH, temperature, and salinity were optimised and 60.2% degradation of crude oil removal was observed in 5days. The strain Y-1 showed strong tolerance to high salinity, alkalinity, and temperature. Emplastic produced by strain Y-1 at high temperatures could be applied as biosurfactant. Gas chromatography analysis demonstrated that the strain Y-1 efficiently degraded different alkanes from crude oil, and the emplastic produced by strain Y-1 promoted the degradation rates of long-chain alkanes when the temperature increased to 55°C. Therefore, strain Y-1 would play an important role in the area of crude oil contaminant bioremediation even in some extreme conditions. PMID:26994837

  11. Bacterial degradation of aromatic pollutants: a paradigm of metabolic versatility

    OpenAIRE

    Díaz Fernández, Eduardo

    2004-01-01

    Although most organisms have detoxification abilities (i.e mineralization, transformation and/or immobilization of pollutants), microorganisms, particularly bacteria, play a crucial role in biogeochemical cycles and in sustainable development of the biosphere. Next to glucosyl residues, the benzene ring is the most widely distributed unit of chemical structure in nature, and many of the aromatic compounds are major environmental pollutants. Bacteria have developed strategies fo...

  12. Determination of the hydrocarbon-degrading metabolic capabilities of tropical bacterial isolates

    Energy Technology Data Exchange (ETDEWEB)

    Marquez-Rocha, F.J.; Olmos-Soto, J. [Centro de Investigacion Cientifica y de Educacion Superior de Ensenada, San Diego, CA (United States). Departamento de Biotecnologia Marina; Rosano-Hernandez, M.A.; Muriel-Garcia, M. [Instituto Mexicano del Petroleo, CD Carmen Camp (Mexico). Zona Marina/Tecnologia Ambiental

    2005-01-01

    Of more than 20 bacteria isolated from a tropical soil using minimal medium supplemented with hydrocarbons, 11 grew well on diesel as sole carbon source, and another 11 grew in the presence of polynuclear aromatic hydrocarbons (PAHs). Ten isolates were identified phenotypically as Pseudomonas sp. and eight as Bacillus sp. Gene sequences representing the catabolic genes (alkM, todM, ndoM, and xylM) and 16S rRNA gene sequences characteristic for Pseudomona and Bacillus were amplified by PCR, using DNA recovered from the supernatant of hydrocarbon-contaminated soil suspensions. Based on their rapid growth characteristics in the presence of hydrocarbons and the formation of PCR products for the catabolic genes alkM and ndoM six isolates were selected for biodegradation assays. After 30 days a mixed culture of two isolates achieved close to 70% hydrocarbon removal and apparent mineralization of 16% of the hydrocarbons present in the soil. Biodegradation rates varied from 275 to 387 mg hydrocarbon kg{sup -1} day{sup -1}. Several bacterial isolates obtained in this study have catabolic capabilities for the biodegradation of alkanes and aromatic hydrocarbons including PAHs. (author)

  13. Comparison of three different in vitro mutation assays used for the investigation of cytochrome P450-mediated mutagenicity of nitro-polycyclic aromatic hydrocarbons

    NARCIS (Netherlands)

    Kappers, W.A.; Och, F.M.M. van; Groene, E.M. de; Horbach, G.J.

    2000-01-01

    Three different in vitro mutation assays were used to investigate the involvement of cytochrome P450 enzymes in the activation of the nitro- polycyclic aromatic hydrocarbons (nitroPAHs) 1-nitropyrene and 2- nitrofluorene and their reduced metabolites amino-polycyclic aromatic hydrocarbons (aminoPAHs

  14. Limitations of microbial hydrocarbon degradation at the Amon Mud Volcano (Nile Deep Sea Fan

    Directory of Open Access Journals (Sweden)

    J. Felden

    2013-01-01

    Full Text Available The Amon mud volcano (MV, located at 1250 m water depth on the Nile Deep Sea Fan, is known for its active emission of methane and non-methane hydrocarbons into the hydrosphere. Previous investigations showed a low efficiency of hydrocarbon-degrading anaerobic microbial communities inhabiting the Amon MV center in the presence of sulphate and hydrocarbons in the seeping subsurface fluids. By comparing spatial and temporal patterns of in situ biogeochemical fluxes, temperature gradients, pore water composition and microbial activities over three years, we investigated why the activity of anaerobic hydrocarbon degraders can be low despite high energy supplies. We found that the central dome of the Amon MV, as well as a lateral mud flow at its base, showed signs of recent exposure of hot subsurface muds lacking active hydrocarbon degrading communities. In these highly disturbed areas, anaerobic degradation of methane was less than 2% of the methane flux. Rather high oxygen consumption rates compared to low sulphide production suggest a faster development of more rapidly growing aerobic hydrocarbon degraders in highly disturbed areas. In contrast, the more stabilized muds surrounding the central gas and fluid conduits hosted active anaerobic hydrocarbon-degrading microbial communities. Furthermore, within three years, cell numbers and hydrocarbon degrading activity increased at the gas-seeping sites. The low microbial activity in the hydrocarbon-vented areas of Amon mud volcano is thus a consequence of kinetic limitations by heat and mud expulsion, whereas most of the outer mud volcano area is limited by hydrocarbon transport.

  15. Energetics and kinetics of anaerobic aromatic and fatty acid degradation. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Michael J. McInerney

    1996-06-24

    The factors that affect the rate and extent of a model aromatic compound, benzoate, in methanogenic environments was studied. Benzoate is degraded to a threshold concentration below which no further substrate degradation occurs. The threshold concentration depended on the substrate concentration and the amount of acetate present. The threshold value was not a function of the kinetic ability of the organism or toxicity of the end products. Rather a minimal Gibb's free energy value may exist where thermodynamic constraints preclude further benzoate degradation. In addition, new bacterial species were isolated and described, that degrade benzoate or reduce iron, cobalt and other metals.

  16. Does glucose enhance the formation of nitrogen containing polycyclic aromatic compounds and polycyclic aromatic hydrocarbons in the pyrolysis of proline?

    Energy Technology Data Exchange (ETDEWEB)

    Phillip F. Britt; A.C. Buchanan; Clyde V. Owens, Jr.; J. Todd Skeen [Oak Ridge National Laboratory, Oak Ridge, TN (United States). Chemical and Analytical Sciences Division

    2004-08-01

    The gas-phase pyrolysis of proline, glucose, 1-((2{prime}-carboxy)pyrrolidinyl)-1-deoxy-D-fructose (the proline Amadori compound), and a 1:1 mixture by weight of proline and glucose was investigated at high temperatures (600-840{sup o}C) and short residence time (i.e. 1.0 s) in an inert atmosphere to determine if glucose or Maillard reaction products enhance the formation of nitrogen containing polycyclic aromatic compounds (N-PACs) and polycyclic aromatic hydrocarbons (PAHs) in the pyrolysis of proline. To study the gas-phase formation of N-PACs and PAHs, the substrates were sublimed into the pyrolysis furnace at 460{sup o}C. Thermogravimetric analysis showed that glucose, the proline/glucose mixture, and the proline Amadori compound undergo solid-state decomposition reactions before subliming. Thus, the substrates were pyrolyzed in two stages: at 460{sup o}C during the sublimation and at 600-840{sup o}C. At 800{sup o}C with a residence time of 1.0 s, proline produced low yields of N-PACs, such as quinoline, isoquinoline, indole, acridine, and carbazole, and PAHs, such as phenanthrene, pyrene, benz(a)anthracene, benzofluoranthene isomers, and benzo(a)pyrene. Increasing the temperature and residence time increased the yield of these products. Under similar pyrolysis conditions, the proline Amadori compound produced 2-8 fold more N-PACs and PAHs than proline. A 1:1 mixture of proline and glucose produced a similar slate of pyrolysis products as the proline Amadori compound, but it is unclear whether the proline Amadori compound was an intermediate in the reaction. In general, the proline Amadori compound produced a higher yield of N-PACs and PAHs than the proline/glucose mixture, but glucose clearly enhances the low temperature gas-phase formation of N-PACs and PAHs from the pyrolysis of proline. 56 refs., 10 figs., 3 tabs.

  17. Assessing the hydrocarbon degrading potential of indigenous bacteria isolated from crude oil tank bottom sludge and hydrocarbon-contaminated soil of Azzawiya oil refinery, Libya.

    Science.gov (United States)

    Mansur, Abdulatif A; Adetutu, Eric M; Kadali, Krishna K; Morrison, Paul D; Nurulita, Yuana; Ball, Andrew S

    2014-09-01

    The disposal of hazardous crude oil tank bottom sludge (COTBS) represents a significant waste management burden for South Mediterranean countries. Currently, the application of biological systems (bioremediation) for the treatment of COTBS is not widely practiced in these countries. Therefore, this study aims to develop the potential for bioremediation in this region through assessment of the abilities of indigenous hydrocarbonoclastic microorganisms from Libyan Hamada COTBS for the biotreatment of Libyan COTBS-contaminated environments. Bacteria were isolated from COTBS, COTBS-contaminated soil, treated COTBS-contaminated soil, and uncontaminated soil using Bushnell Hass medium amended with Hamada crude oil (1 %) as the main carbon source. Overall, 49 bacterial phenotypes were detected, and their individual abilities to degrade Hamada crude and selected COBTS fractions (naphthalene, phenanthrene, eicosane, octadecane and hexane) were evaluated using MT2 Biolog plates. Analyses using average well colour development showed that ~90 % of bacterial isolates were capable of utilizing representative aromatic fractions compared to 51 % utilization of representative aliphatics. Interestingly, more hydrocarbonoclastic isolates were obtained from treated contaminated soils (42.9 %) than from COTBS (26.5 %) or COTBS-contaminated (30.6 %) and control (0 %) soils. Hierarchical cluster analysis (HCA) separated the isolates into two clusters with microorganisms in cluster 2 being 1.7- to 5-fold better at hydrocarbon degradation than those in cluster 1. Cluster 2 isolates belonged to the putative hydrocarbon-degrading genera; Pseudomonas, Bacillus, Arthrobacter and Brevundimonas with 57 % of these isolates being obtained from treated COTBS-contaminated soil. Overall, this study demonstrates that the potential for PAH degradation exists for the bioremediation of Hamada COTBS-contaminated environments in Libya. This represents the first report on the isolation of

  18. Study of the interaction between water and hydrogen sulfide with polycyclic aromatic hydrocarbons.

    Science.gov (United States)

    Cabaleiro-Lago, Enrique M; Carrazana-García, Jorge A; Rodríguez-Otero, Jesús

    2009-06-21

    A computational study has been carried out for determining the characteristics of the interaction between one water and hydrogen sulfide molecule with a series of polycyclic aromatic hydrocarbons of increasing size, namely, benzene, anthracene, triphenylene, coronene, circumcoronene, and dicircumcoronene. Potential energy curves were calculated for structures where H(2)X (X=O,S) molecule is located over the central six-membered ring with its hydrogen atoms pointing toward to (mode A) or away from (mode B) the hydrocarbon. The accuracy of different methods has been tested against the results of coupled cluster calculations extrapolated to basis set limit for the smaller hydrocarbons. The spin component scaled MP2 (SCS-MP2) method and a density functional theory method empirically corrected for dispersion (DFT-D) reproduce fairly well the results of high level calculations and therefore were employed for studying the larger systems, though DFT-D seems to underestimate the interaction in hydrogen sulfide clusters. Water complexes in mode A have interaction energies that hardly change with the size of the hydrocarbon due to compensation between the increase in the correlation contribution to the interaction energy and the increase in the repulsive character of the Hartree-Fock energy. For all the other clusters studied, there is a continuous increase in the intensity of the interaction as the size of the hydrocarbon increases, suggesting already converged values for circumcoronene. The interaction energy for water clusters extrapolated to an infinite number of carbon atoms amounts to -13.0 and -15.8 kJ/mol with SCS-MP2 and DFT-D, respectively. Hydrogen sulfide interacts more strongly than water with the hydrocarbons studied, leading to a limiting value of -21.7 kJ/mol with the SCS-MP2 method. Also, complexes in mode B are less stable than the corresponding A structures, with interaction energies amounting to -8.2 and -18.2 kJ/mol for water and hydrogen sulfide

  19. Limitations of microbial hydrocarbon degradation at the Amon mud volcano (Nile deep-sea fan)

    NARCIS (Netherlands)

    Felden, J.; Lichtschlag, A.; Wenzhöfer, F.; de Beer, D.; Feseker, T.; Pop Ristova, P.; de Lange, G.; Boetius, A.

    2013-01-01

    The Amon mud volcano (MV), located at 1250m water depth on the Nile deep-sea fan, is known for its active emission of methane and non-methane hydrocarbons into the hydrosphere. Previous investigations showed a low efficiency of hydrocarbon-degrading anaerobic microbial communities inhabiting the Amo

  20. Distribution of Polycyclic aromatic hydrocarbons between water, sediment and common eels (Anguilla angillae) in the urban stretch of Tevere River

    International Nuclear Information System (INIS)

    The research has focused the attention on the occurrence of polycyclic aromatic hydrocarbons (PAHs) in water, sediment and common eels (Angilla anguillae) in the urban area of Tevere River. These compounds can derived from point (E.g.oil spill) or non-point (e.g. atmospheric deposition) sources and are one of the most widespread organic pollutants. (Author)

  1. Analysis of polycyclic aromatic hydrocarbons. I. Determination by gas chromatography with glass and fused solica capillary columns

    International Nuclear Information System (INIS)

    A study of the analysis by gas chromatography of aromatic polycyclic hydrocarbons is presented. The separation has been carried out by glass and fused silice capillary column. The limitations and the advantages of the procedure are discussed in terms of separation efficiency, sensitivity and precision. (author). 3 figs., 17 refs

  2. Analysis of polycyclic aromatic hydrocarbons I. Determination by gas chromatography with glass and fused silica capillary columns

    International Nuclear Information System (INIS)

    A study of the analysis by gas chromatography of aromatic polycyclic hydrocarbons is presented. The separation has been carried out by glass and fused silica capillary column. The limitations and the advantages of the procedure are discussed in terms of separation efficiency, sensitivity and precision. (Author) 17 refs

  3. Repair of DNA damage induced by anthanthrene, a polycyclic aromatic hydrocarbon (PAH) without bay or fjord regions

    DEFF Research Database (Denmark)

    Madsen, Claus Desler; Johannessen, Christian; Rasmussen, Lene Juel

    2009-01-01

    Polycyclic aromatic hydrocarbons (PAHs) are environmental pollutants, formed during incomplete burning of coal, oil and gas. Several PAHs have carcinogenic and mutagenic potencies, but these compounds must be activated in order to exert their mutagenic effects. One of the principal pathways...

  4. Breast cancer and urinary biomarkers of polycyclic aromatic hydrocarbon and oxidative stress in the Shanghai Women’s Health Study

    OpenAIRE

    Lee, Kyoung-Ho; Shu, Xiao-Ou; Gao, Yu-Tang; Ji, Bu-Tian; YANG, Gong; Blair, Aaron; Rothman, Nathaniel; Zheng, Wei; Chow, Wong-Ho; Kang, Daehee

    2010-01-01

    Polycyclic aromatic hydrocarbon (PAH) exposures and oxidative stress from such and other exposures have been associated with breast cancer in some studies. To further evaluate the role of PAH metabolites and oxidative stress on the development of breast cancer, we conducted a nested case-control study in the Shanghai Women’s Health Study (SWHS).

  5. Monitoring of polycyclic aromatic hydrocarbons (PAH) in food supplements containing botanicals and other ingredients on the Dutch market

    NARCIS (Netherlands)

    Martena, M.J.; Grutters, M.; Groot, de H.N.; Konings, E.J.M.; Rietjens, I.

    2011-01-01

    Food supplements can contain polycyclic aromatic hydrocarbons (PAH). The European Food Safety Authority (EFSA) has defined 16 priority PAH that are both genotoxic and carcinogenic and identified eight priority PAH (PAH8) or four of these (PAH4) as good indicators of the toxicity and occurrence of PA

  6. Novel magnetic nanoparticles coated by benzene- and β-cyclodextrin-bearing dextran, and the sorption of polycyclic aromatic hydrocarbon

    DEFF Research Database (Denmark)

    Cho, Eunae; Tahir, Muhammad Nazir; Min Choi, Jae;

    2015-01-01

    , the potential for removing polycyclic aromatic hydrocarbons such as phenanthrene and pyrene by sorption onto the nanomaterials was assessed. In the sorption, pi-stacking interactions of the benzene-derivatized dextran and host–guest chemistry of the β-cyclodextrin-derivatized dextran were considered...

  7. 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

  8. Impact of polychlorinated biphenyl and polycyclic aromatic hydrocarbon sequestration in sediment on bioaccumulation in aquatic food webs

    NARCIS (Netherlands)

    Moermond, C.T.A.; Roessink, I.; Jonker, M.T.O.; Meijer, T.; Koelmans, A.A.

    2007-01-01

    It is not clear whether sequestration or aging of organic chemicals like polychlorinated biphenyls (PCBs) and polycyclic aromatic hydrocarbons (PAHs) limits accumulation in higher levels of aquatic food chains. Therefore, the effect of aging on accumulation was studied in 1-m3 model ecosystems that

  9. THE PENALIZED OPTIMAL EXPERIMENTAL DESIGN: THE PRECISE ESTIMATION OF AN INTERACTION THRESHOLD IN A MIXTURE OF EIGHTEEN POLYHALOGENATED AROMATIC HYDROCARBONS.

    Science.gov (United States)

    Crofton et al. (EHP, 2005) conducted a study of 18 polyhalogenated aromatic hydrocarbons (PHAHs) on serum total thyroxine (T4). Young female Long-Evans rats were dosed with the 18 single agents or a fixed-ratio mixture, and serum total T4 was measured via radioimmunoassay. The i...

  10. Biodegradation of polycyclic aromatic hydrocarbons (PAHs) by native microflora and combinations of white-rot fungi in a coal-tar contaminated soil

    Energy Technology Data Exchange (ETDEWEB)

    Canet, R.; Birnstingl, J.G.; Malcolm, D.G.; Lopez-Real, J.M.; Beck, A.J. [Inst. of Valenciano Invest. Agency, Valencia (Spain)

    2001-07-01

    Four white-rot fungi (Phanerochaete chrysosporium IMI 232175, Pleurotus ostreatus from the University of Alberta Microfungus Collection IMI 341687, Coriolus versicolor IMI210866 and Wye isolate No. 7) and all possible combinations of two or more of these fungi, were incubated in microcosms containing wheat straw and non-sterile coal-tar contaminated soil to determine their potential to degrade polycyclic aromatic hydrocarbons (PAHs). Biotic and abiotic controls were prepared similarly and PAH concentrations remaining in each microcosm were determined after 8, 16 and 32 weeks by GC-MS following extraction with dichloromethane. The greatest PAH losses were in the biotic control. Soil cultures prepared at the end of the experiment showed that though introduced fungi were still alive, they were unable to thrive and degrade PAH in such a highly contaminated soil and remained in a metabolically inactive form.

  11. Isolation and Screening of Hydrocarbon Degrading Bacterial Strains for Bioremediation of Petroleum Pollution in Qatar

    OpenAIRE

    Al Disi, Zulfa Ali

    2013-01-01

    Pollution, due to activities related to the oil industry, represents a serious threat to the natural environment. The application of biotechnological methods provides much safer and sustainable alternatives for bioremediation of polluted areas, using microorganisms. Several techniques for the isolation of hydrocarbon degrading bacteria have been investigated and published worldwide. A wide range of bilogical activities was shown. However, local hydrocarbon degrading strains and the factors af...

  12. Influence of smoking parameters on the concentration of polycyclic aromatic hydrocarbons (PAHs) in Danish smoked fish

    DEFF Research Database (Denmark)

    Duedahl-Olesen, Lene; Christensen, J. H.; Højgård, A.;

    2010-01-01

    smoking, and for other fish species direct smoking leads to higher sigma PAH25 than indirect smoking. Also, the usage of common alder increases the PAH contamination compared with beech. The effects of smoking time, combustion temperatures, and two types of smoke-generating material on the Sigma PAH25......A new method for the analysis of 25 polycyclic aromatic hydrocarbon (PAH) compounds in fish was developed, validated, and used for the quantification of PAHs in 180 industrially smoked fish products. The method included pressurized liquid extraction, gel-permeation chromatography (Bio-beads S-X3...... concentrations were obtained for indirectly smoked trout (26 mu g kg-1). Principal component analysis was used to correlate processing parameters to PAH concentrations and to identify the effects of these parameters. The analysis showed that for salmon hot-smoking conditions lead to higher sigma PAH25 than cold...

  13. Overview of established and emerging treatment technologies for polycyclic aromatic hydrocarbons at wood preserving facilities

    International Nuclear Information System (INIS)

    The contamination of soil and groundwater by polycyclic aromatic hydrocarbons (PAHs) is common to wood preserving facilities and manufactured gas plants. Since the inception of RCRA and CERCLA, much attention has been focused upon the remediation of both active and defunct wood preserving facilities. The experiences gleaned from the use of proven technologies, and more importantly, the lessons being learned in the trials of emerging technologies on creosote-derived PAH clean-ups at wood preserving sites, should have direct bearing on the clean-up of similar contaminants at MGP sites. In this paper, a review of several remedial actions using waste removal/disposal, on-site incineration, and bioremediation will be presented. Additionally, emerging technologies for the treatment of PAH-contaminated soil and water will be reviewed. Lastly, recent information on risk assessment results for creosote sites and treated PAH waste will be discussed

  14. Source apportionment of polycyclic aromatic hydrocarbons (PAHs) in sediments from Khuzestan province, Iran

    DEFF Research Database (Denmark)

    Lübeck, Josephine; Poulsen, Kristoffer Gulmark; Knudsen, Sofie B.;

    2016-01-01

    Khuzestan, Iran is heavily industrialised with petrochemical and refinery companies. Herein, sediment and soil samples were collected from Hendijan coast, Khore Mosa and Arvandroud River. The CHEMSIC (CHEmometric analysis of Selected Ion Chromatograms) method was used to assign the main sources...... of polycyclic aromatic hydrocarbon (PAH) pollution. A four-component principal component analysis (PCA) model was obtained. While principal component 1 (PC1) was related to the total concentration of PAHs, the remaining PCs described three distinct sources: PC2 and PC3 collectively differentiate between...... weathered petrogenic and pyrogenic, and PC4 is indicative for a diagenetic input. The sources of PAHs in the Arvandroud River were mainly relatively fresh oil with some samples corresponding to a weathered oil input. Further, perylene (indicator for diagenetic source) was identified. Samples from Khore Mosa...

  15. Atmospheric polycyclic aromatic hydrocarbons (PAHs) in Asia: A review from 1999 to 2004

    International Nuclear Information System (INIS)

    Polycyclic aromatic hydrocarbons (PAHs) are present in both gaseous and particulate phases. These compounds are considered to be atmospheric contaminants and are human carcinogens. Many studies have monitored atmospheric particulate and gaseous phases of PAH in Asia over the past 5 years. This work compares and discusses different sample collection, pretreatment and analytical methods. The main PAH sources are traffic exhausts (AcPy, FL, Flu, PA, Pyr, CHR, BeP) and industrial emissions (BaP, BaA, PER, BeP, COR, CYC). PAH concentrations are highest in areas of traffic, followed by the urban sites, and lowest in rural sites. Meteorological conditions, such as temperature, wind speed and humidity, strongly affect PAH concentrations at all sampling sites. This work elucidates the characteristics, sources and distribution, and the healthy impacts of atmospheric PAH species in Asia. - This work summarizes the characteristics, sources and distribution, and the healthy impacts of atmospheric PAH species in Asia

  16. Role of volcanic dust in the atmospheric transport and deposition of polycyclic aromatic hydrocarbons and mercury.

    Science.gov (United States)

    Stracquadanio, Milena; Dinelli, Enrico; Trombini, Claudio

    2003-12-01

    The role of volcanic ash as scavenger of atmospheric pollutants, in their transport and final deposition to the ground is examined. Attention is focused on polycyclic aromatic hydrocarbons (PAHs) and on particulate mercury (Hgp). The ash-fall deposits studied belong to the 2001 and 2002 eruptive activity of Mount Etna, Southern Italy, and were investigated at three (2001) and four (2002) sites downwind of the major tephra dispersal pattern. The dry deposition of mercury and PAHs was determined, and, in particular, a downward flux to the ground of PAHs (approximately 7.29 microg m(-2) per day) and mercury (750 ng m(-2) per day) was estimated in Catania from October 26 to October 28, 2002. Finally, evidence on the anthropogenic origin of PAHs scavenged from the troposphere by volcanic ash is supported by the analysis of PAH compositions in granulometrically homogeneous fractions.

  17. Biotransformation of the polycyclic aromatic hydrocarbon pyrene in the marine polychaete Nereis virens

    DEFF Research Database (Denmark)

    Jørgensen, Anne; Glessing, Anders M B; Rasmussen, Lene Juel;

    2005-01-01

    In vivo and in vitro biotransformation of the polycyclic aromatic hydrocarbon (PAH) pyrene was investigated in the marine polychaete Nereis virens. Assays were designed to characterize phase I and II enzymes isolated from gut tissue. High-pressure liquid chromatography measurement of 1......-hydroxypyrene, pyrene-1-glucuronide, pyrene-1-sulfate, and pyrene-1-glucoside appeared to be a sensitive method for estimating the activity of pyrene hydroxylase, glucuronosyl transferase, and sulfotransferase. Total pyrene in gut tissue after a 5-d exposure to 10 microg/g dry weight pyrene constituted 65....... Apparent kinetic parameters for pyrene hydroxylase activity were changed after induction with pyrene. Induced worms showed increased Vmax(a)) and decreased Km(a) compared to noninduced worms, indicating that the relative amount of the cytochrome P450 enzyme(s) responsible for pyrene hydroxylation...

  18. Polycyclic aromatic hydrocarbons alter the structure of oceanic and oligotrophic microbial food webs

    KAUST Repository

    Cerezo, Maria Isabel

    2015-11-01

    One way organic pollutants reach remote oceanic regions is by atmospheric transport. During the Malaspina-2010 expedition, across the Atlantic, Indian, and Pacific Oceans, we analyzed the polycyclic aromatic hydrocarbon (PAH) effects on oceanic microbial food webs. We performed perturbation experiments adding PAHs to classic dilution experiments. The phytoplankton growth rates were reduced by more than 5 times, being Prochlorococcus spp. the most affected. 62% of the experiments showed a reduction in the grazing rates due to the presence of PAHs. For the remaining experiments, grazing usually increased likely due to cascading effects. We identified changes in the slope of the relation between the growth rate and the dilution fraction induced by the pollutants, moving from no grazing to V-shape, or to negative slope, indicative of grazing increase by cascade effects and alterations of the grazers\\' activity structure. Our perturbation experiments indicate that PAHs could influence the structure oceanic food-webs structure.

  19. Emission factors of carbonaceous particulate matter and polycyclic aromatic hydrocarbons from residential solid fuel combustions

    Energy Technology Data Exchange (ETDEWEB)

    Shen, Guofeng [Jiangsu Academy of Environmental Science, Nanjing (China). Inst. of Atmospheric Sciences

    2014-07-01

    Emission inventory is basic for the understanding of environmental behaviors and potential effects of compounds, however, current inventories are often associated with relatively high uncertainties. One important reason is the lack of emission factors, especially for the residential solid fuel combustion in developing countries. In the present study, emission factors of a group of pollutants including particulate matter, organic carbon, elemental carbon (sometimes known as black carbon) and polycyclic aromatic hydrocarbons were measured for a variety of residential solid fuels including coal, crop straw, wood, and biomass pellets in rural China. The study provided a large number of emission factors that can be further used in emission estimation. Composition profiles and isomer ratios were investigated and compared so as to be used in source apportionment. In addition, the present study identified and quantified the influence of factors like fuel moisture, volatile matter on emission performance.

  20. Estimation and characterization of polycyclic aromatic hydrocarbons from magnesium metallurgy facilities in China.

    Science.gov (United States)

    Nie, Zhiqiang; Yang, Yufei; Tang, Zhenwu; Liu, Feng; Wang, Qi; Huang, Qifei

    2014-11-01

    Field monitoring was conducted to develop a polycyclic aromatic hydrocarbon (PAH) emission inventory for the magnesium (Mg) metallurgy industry in China. PAH emissions in stack gas and fly/bottom ash samples from different smelting units of a typical Mg smelter were measured and compared. Large variations of concentrations, congener patterns, and emission factors of PAHs during the oxidation and reduction stages in the Mg smelter were observed. The measured average emission factor (166,487 μg/t Mg) was significantly higher than those of other industrial sources. Annual emission from Mg metallurgy in 2012 in China was estimated at 116 kg (514 g BaPeq) for PAHs. The results of this study suggest that PAH emission from Mg industries should be considered by local government agencies. These data may be helpful for understanding PAH levels produced by the Mg industry and in developing a PAH inventory.

  1. [Assessment of exposure to cancerogenic aromatic hydrocarbon during controlled-access highways management activities].

    Science.gov (United States)

    Martinotti, I; Cirla, A M; Cottica, D; Cirla, P E

    2011-01-01

    The purpose of this study was an integrated assessment of exposure to benzene and Polycyclic Aromatic Hydrocarbons (PAH) in 29 workers employed to manage a controlled-access highways. A campaign was performed in summertime by environmental monitoring (active and passive airborne personal sampler), as well as by biological monitoring (urine samples of the beginning and of the end of daily shift, baseline after two days of vacation). The measured environmental levels did not differ from background environmental concentrations found in a metropolitan area (i.e. benzo[a]pyrene < 1 ng/m3; benzene < 5 mcg/m3), and the results of biological monitoring were in agreement and were compatible with extra-professional habits of the investigated subjects (1-hydroxipyrene 50-990 ng/g creatinine; unmetabolized benzene 15-2010 ng/I; t-t muconic acid < 4-222 mcg/g creatinine).

  2. Trapping of polycyclic aromatic hydrocarbons by amphiphilic cyclodextrin functionalized polypropylene nonwovens

    DEFF Research Database (Denmark)

    Lumholdt, Ludmilla; Nielsen, Ronnie Bo Højstrup; Larsen, Kim Lambertsen

    Recently, there has been an augmented focus on the increasing amount of pesticides, drug residues and endocrine disruptors present in waste and drinking water1. These pollutants represent a challenge in water purification since they may be hazardous to human health even in low doses2. Cyclodextrins...... of the textile fibers. In this study we present the ability of amphiphilic CD coated polypropylene nonwovens to trap 8 different polycyclic aromatic hydrocarbons/endocrine disruptors from aqueous solutions thus demonstrating the potential of using the amphiphilic cyclodextrins for water purification....... (CDs) are known to be able to form inclusion complexes with a large range of the unwanted pollutantse.g. 3 but in order to utilise this ability to purify water, the CDs must be immobilised on a surface, for instance, a membrane filter. We have developed a simple and fast method...

  3. Distribution and origin sources of Polycyclic Aromatic Hydrocarbons (PAHs) pollution in sediment of Sarawak coastal area

    International Nuclear Information System (INIS)

    Alkyl and parent Polycyclic Aromatic Hydrocarbons (PAHs) compounds in marine sediment sample collected from ten locations along Sarawak coastal areas were extracted and analyzed by using gas chromatography-mass spectrometry. The source identification of PAH pollution in marine sediment of Sarawak coastal areas were identify by ratios technique of An/ An+phen, Fl/ Fl +Py, B[a]A/ (B[a]A+Chry) and total Methyl Phen/ Phen. The total alkyl and parent PAHs concentration varies from 36.5 - 277.4 ng/ g dry weight (d.w.) with a mean concentration of 138.2 ng/ g d.w. The ratio values of PAHs pollution in marine sediment of Sarawak coastal areas are clearly indicating the PAHs pollutions are originated from petroleum (petrogenic) and petroleum combustion (pyrolytic). However, the origin sources of PAHs pollution in a few stations were uncertain due to mixing sources of PAHs. (author)

  4. Use of antioxidant enzymes of clam Ruditapes philippinarum as biomarker to polycyclic aromatic hydrocarbon pollution

    Science.gov (United States)

    Zhu, Lin; Tang, Xuexi; Wang, Ying; Sui, Yadong; Xiao, Hui

    2016-03-01

    The typical organic pollutant polycyclic aromatic hydrocarbon (PAH) anthracene was selected as a contaminant to investigate its effects on the activities of superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GSH-Px) in the clam Ruditapes philippinarum. The results show that SOD, CAT and GSH-Px had diff erent induction and inhibition reactions to anthracene stress, and that three diff erent organs in R. philippinarum (visceral mass, muscle tissue and mantle) had diff erent sensitivities to anthracene stress. This study suggest that SOD activities of the visceral mass, CAT activitities of the mantle and the visceral mass, and GSH-Px activity of the muscle tissue could be used as sensitive indicators of anthracene stress in R. philippinarum.

  5. Extraction agents for the removal of polycyclic aromatic hydrocarbons (PAHs) from soil in soil washing technologies.

    Science.gov (United States)

    Lau, Ee Von; Gan, Suyin; Ng, Hoon Kiat; Poh, Phaik Eong

    2014-01-01

    Polycyclic aromatic hydrocarbons (PAHs) in soil have been recognised as a serious health and environmental issue due to their carcinogenic, mutagenic and teratogenic properties. One of the commonly employed soil remediation techniques to clean up such contamination is soil washing or solvent extraction. The main factor which governs the efficiency of this process is the solubility of PAHs in the extraction agent. Past field-scale soil washing treatments for PAH-contaminated soil have mainly employed organic solvents or water which is either toxic and costly or inefficient in removing higher molecular weight PAHs. Thus, the present article aims to provide a review and discussion of the alternative extraction agents that have been studied, including surfactants, biosurfactants, microemulsions, natural surfactants, cyclodextrins, vegetable oil and solution with solid phase particles. These extraction agents have been found to remove PAHs from soil at percentages ranging from 47 to 100% for various PAHs. PMID:24100092

  6. Study on Removing Trace Olefins in Aromatic Hydrocarbons with HPMo-loaded Y Zeolites

    Institute of Scientific and Technical Information of China (English)

    Jiang Zhenghong; Zeng Haiping; Shi Li

    2008-01-01

    HPMo-loaded Y-zeolites were prepared for the removal of trace olefins from aromatic hydrocarbons.The temperature of calcination and the proportion of phospho-molybdic acid in the catalyst were studied. The catalytic activity for olefins removal and the service life of the catalyst were tested in a fixed bed microreactor. The results showed that the catalyst containing 3% phospho-molybdic acid, which was calcined at 550℃,demonstrated the best activity for olefins removal. The catalyst could be regenerated and could perform still very well. Catalyst characterization was performed by XRD and measured by pyridine-FTIR spectrometry. The test results indicated that the activity of the catalyst was related with the effect of acid concentration and acid strength. Besides, the deactivation of the catalyst was associated with the formation of coke deposits and the deactivated catalyst could recover its activity by oxidation with air under a proper temperature.

  7. Qualitative TLC determination of some polycyclic aromatic hydrocarbons in sugar-beet

    Directory of Open Access Journals (Sweden)

    BILJANA D. SKRBIC

    2005-10-01

    Full Text Available The presence of polycyclic or polynuclear aromatic hydrocarbons (PAHs were investigated in sugar-beet from a local sugar factory in the district of Vojvodina. The sugar-beet was cultivated on areas near roads with intensive traffic. The procedure for the preparation and determination of these compounds included saponification of the sample, several liquid–liquid extraction systems and a silica gel column clean-up. The purified sample solution was analysed by thin layer chromatography (TLC on silica gel with cyclohexane as the developing solvent. Benzo(bfluoranthene and benzo(aanthracene and/or benzo(apyrene were detected at concentrations greater than the allowed limits in food.

  8. Enhanced diffusion of polycyclic aromatic hydrocarbons in artificial and natural aqueous solutions

    DEFF Research Database (Denmark)

    Mayer, Philipp; Fernqvist, M.M.; Christensen, P.S.;

    2007-01-01

    Uptake of hydrophobic organic compounds into organisms is often limited by the diffusive transport through a thin boundary layer. Therefore, a microscale diffusion technique was applied to determine the diffusive mass transfer of 12 polycyclic aromatic hydrocarbons through water, air, surfactant...... solutions, humic acid solutions, aqueous soil and horse manure extracts, digestive fluid of a deposit-feeding worm, and root exudates from willow plants. In most cases the diffusive mass transfer of PAHs was much higher through the tested media than through water, and the enhancement factors increased...... with increasing hydrophobicity of the PAHs. The diffusive flux of benzo[a]pyrene was for instance enhanced 74 times through gut fluid of a deposit-feeding worm when compared to water. These findings demonstrate that a wide variety of dissolved organic carbon (DOC) at environmental levels can enhance diffusive...

  9. On-line database of the spectral properties of polycyclic aromatic hydrocarbons

    CERN Document Server

    Malloci, G; Mulas, G; 10.1016/j.chemphys.2007.01.001

    2009-01-01

    We present an on-line database of computed molecular properties for a large sample of polycyclic aromatic hydrocarbons (PAHs) in four charge states: -1, 0, +1, and +2. At present our database includes 40 molecules ranging in size from naphthalene and azulene (C10H8) up to circumovalene (C66H20). We performed our calculations in the framework of the density functional theory (DFT) and the time-dependent DFT to obtain the most relevant molecular parameters needed for astrophysical applications. For each molecule in the sample, our database presents in a uniform way the energetic, rotational, vibrational, and electronic properties. It is freely accessible on the web at http://astrochemistry.ca.astro.it/database/ and http://www.cesr.fr/~joblin/database/.

  10. Polycyclic aromatic hydrocarbons in blood related to lower body mass in common loons.

    Science.gov (United States)

    Paruk, James D; Adams, Evan M; Uher-Koch, Hannah; Kovach, Kristin A; Long, Darwin; Perkins, Christopher; Schoch, Nina; Evers, David C

    2016-09-15

    We captured 93 wintering adult and subadult Common Loons (Gavia immer) in coastal Louisiana from 2011 to 2015 following the Deepwater Horizon oil spill. We tested blood samples for exposure to polycyclic aromatic hydrocarbons (PAHs) and measured physiological variables including hematocrit, hemoglobin and total blood protein. PAH concentrations in loon blood differed from year to year and by age class. High PAH concentrations were significantly related to lower body masses in both adult and subadult birds and higher serum protein levels in adults only. PAH concentrations had marginal relations with both hematocrit and hemoglobin levels. The types of PAHs detected also underwent a major shift over time. The PAHs detected in 2011, 2012, and 2015 were primarily low molecular weight (three carbon rings); however, in 2013, most detected PAHs were high molecular weight (four carbon rings). It is unclear what events led to the increase in PAH concentrations and the shift in type of PAHs over time. PMID:27177142

  11. Polycyclic aromatic hydrocarbons and total extractable particulate organic matter in the Arctic aerosol

    International Nuclear Information System (INIS)

    Samples of total suspended particulate matter were collected in March and August 1979 at Barrow, Alaska, a remote site in the Arctic. Ambient concentrations of extractable particulate organic matter (POM), of polycyclic aromatic hydrocarbons (PAH) and of 210Pb were determined. The samples were also examined by optical and scanning electron microscopy. Average concentrations of POM and PAH were similar to those reported for other remote sites in the northern hemisphere, but the concentrations were considerably higher in March than in August. The presence of fly ash in the samples collected during the March sampling period, as well as seasonal differences in the concentrations of the organic species and 210Pb and in meteorology indicate that the principal source of POM and PAH was fossil fuel combustion in the mid-latitudes during the March sampling period. (author)

  12. Application of random forests method to predict the retention indices of some polycyclic aromatic hydrocarbons.

    Science.gov (United States)

    Goudarzi, N; Shahsavani, D; Emadi-Gandaghi, F; Chamjangali, M Arab

    2014-03-14

    In this work, a quantitative structure-retention relationship (QSRR) investigation was carried out based on the new method of random forests (RF) for prediction of the retention indices (RIs) of some polycyclic aromatic hydrocarbon (PAH) compounds. The RIs of these compounds were calculated using the theoretical descriptors generated from their molecular structures. Effects of the important parameters affecting the ability of the RF prediction power such as the number of trees (nt) and the number of randomly selected variables to split each node (m) were investigated. Optimization of these parameters showed that in the point m=70, nt=460, the RF method can give the best results. Also, performance of the RF model was compared with that of the artificial neural network (ANN) and multiple linear regression (MLR) techniques. The results obtained show the relative superiority of the RF method over the MLR and ANN ones.

  13. Correlation of levels of volatile versus carcinogenic particulate polycyclic aromatic hydrocarbons in air samples from smokehouses

    DEFF Research Database (Denmark)

    Hansen, Åse Marie; Poulsen, O M; Christensen, J M

    1991-01-01

    In the present study, data on the concentration of polycyclic aromatic hydrocarbons (PAH) in air samples from fish smokehouses (Nordholm et al. 1986) and meat smokehouses (Hansen et al. submitted for publication) were used to analyze the extent to which six different volatile PAH compounds could...... carcinogenic PAH compounds in air samples from smokehouses, whereas fluoranthene and pyrene displayed the highest specificity. However, when the applicability of the six markers was tested on air samples from iron foundries, only naphthalene and pyrene were useful as markers for the carcinogenic compounds...... function as markers for the total concentration of six different carcinogenic particulate PAH compounds. Although a significant positive correlation was observed between the concentration of each of six volatile compounds and the total concentration of carcinogenic PAH compounds, a particularly good...

  14. Epigenetic modulation of Chlorella (Chlorella vulgaris) on exposure to polycyclic aromatic hydrocarbons.

    Science.gov (United States)

    Yang, Mihi; Youn, Je-In; Kim, Seung Joon; Park, Jong Y

    2015-11-01

    DNA methylation in promoter region can be a new chemopreventive marker against polycyclic aromatic hydrocarbons (PAHs). We performed a randomized, double blind and cross-over trial (N=12 healthy females) to evaluate chlorella (Chlorella vulgaris)-induced epigenetic modulation on exposure to PAHs. The subjects consumed 4 tablets of placebo or chlorella supplement (total chlorophyll ≈ 8.3mg/tablet) three times a day before meals for 2 weeks. When the subjects consumed chlorella, status of global hypermethylation (5-methylcytosine) was reduced, compared to placebo (p=0.04). However, DNA methylation at the DNMT1 or NQO1 was not modified by chlorella. We observed the reduced levels of urinary 1-hydroxypyrene (1-OHP), a typical metabolite of PAHs, by chlorella intake (pchlorella-induced changes in global hypermethylation and urinary 1-OHP (pchlorella works for PAH-detoxification through the epigenetic modulation, the interference of ADME of PAHs and the interaction of mechanisms.

  15. Heavy metals and polycyclic aromatic hydrocarbons in surface sediments of Karoon River, Khuzestan Province, Iran.

    Science.gov (United States)

    Keshavarzi, Behnam; Mokhtarzadeh, Zeinab; Moore, Farid; Rastegari Mehr, Meisam; Lahijanzadeh, Ahmadreza; Rostami, Soqra; Kaabi, Helena

    2015-12-01

    Karoon is the longest river in Iran and provides water for industries located along its banks, such as metal, petrochemical, and oil industries. It is also the source of drinking water for cities such as Ahwas, Abadan, and Khorramshahr. In this study, 34 and 18 surface sediment samples were collected and analyzed for heavy metals (Al, As, Cd, Cr, Cu, Hg, Ni, Pb, and Zn) and polycyclic aromatic hydrocarbons (PAHs). The measured concentrations of heavy metals were compared with US EPA sediment quality guidelines, and the results showed that Cu concentration was above the threshold effect level (TEL) in 65.67% of the samples and Hg concentration was above the effect range median (ERM) in some samples. The results revealed that Hg was severely enriched (5 factory and Abadan petrochemical complex. Principal component analysis and cluster analysis also revealed the relationships between the studied parameters and identified their probable sources. PMID:26233736

  16. Extraction of polycyclic aromatic hydrocarbons from smoked fish using pressurized liquid extraction with integrated fat removal

    DEFF Research Database (Denmark)

    Lund, Mette; Duedahl-Olesen, Lene; Christensen, Jan H.

    2009-01-01

    extraction with fat retention in one single analytical step. The PLE parameters: type of fat retainer, flush volume, solvent composition, fat-to-fat retainer ratio (FFR), and the dimensions of the extraction cells were the most important factors for obtaining fat-free extracts with high recoveries of PAHs. A...... 100 mL extraction cell filled with 18 g activated silica gel, dichloromethane:hexane (15:85, v/v) as extraction solvent, FFR of 0.025 and 100% flush volume was the best analytical setup for integrated extraction and fat retention. The one-step procedure provided a more rapid and cost......Quantification of polycyclic aromatic hydrocarbons (PAHs) in smoked fish products often requires multiple clean-up steps to remove fat and other compounds that may interfere with the chemical analysis. We present a novel pressurized liquid extraction (PLE) method that integrates exhaustive...

  17. THE INFRARED SPECTRA OF POLYCYCLIC AROMATIC HYDROCARBONS WITH SOME OR ALL HYDROGEN ATOMS REMOVED

    Energy Technology Data Exchange (ETDEWEB)

    Bauschlicher, Charles W. Jr. [Entry Systems and Technology Division, Mail Stop 230-3, NASA Ames Research Center, Moffett Field, CA 94035 (United States); Ricca, Alessandra, E-mail: Charles.W.Bauschlicher@nasa.gov, E-mail: Alessandra.Ricca-1@nasa.gov [Carl Sagan Center, SETI Institute, 189 Bernardo Avenue, Mountain View, CA 94043 (United States)

    2013-10-20

    The loss of one hydrogen from C{sub 96}H{sub 24} does not significantly affect the infrared spectra of the neutral, cation, or anion. Excluding a very weak C-C stretching band at 5.1 μm, the loss of two adjacent duo hydrogens does not significantly affect the spectra compared with the parent. Removing all of the hydrogen atoms significantly increases the intensity of the new C-C stretching band, and, for the cation, shifts it to a longer (5.2 μm) wavelength. Observations show a feature near 5.25 μm, which has been attributed to overtone and combination bands from polycyclic aromatic hydrocarbons (PAHs). This current work suggests that dehydrogenated PAHs might also contribute to this band, but its weakness implies that fully dehydrogenated cationic or dicationic species are very rare.

  18. Estimation of cytogenetic risk among coke oven workers exposed to polycyclic aromatic hydrocarbons.

    Science.gov (United States)

    Sureshkumar, Shanmugam; Balachandar, Vellingiri; Devi, Subramaniam Mohana; Arun, Meyyazhagan; Karthickkumar, Alagamuthu; Balamuralikrishnan, Balasubramanian; Sankar, Kathannan; Mustaqahamed, Shafi Ahammed Khan; Dharwadkar, Shanwaz N; Sasikala, Keshavarao; Cho, Ssang-Goo

    2013-01-01

    Polycyclic aromatic hydrocarbons (PAHs) result from the incomplete combustion of natural or synthetic organic materials. The working environment at a coke plant can negatively affect the employed workers who were exposed to coke oven emissions containing PAHs, which formed and released into the environment by the process of pyrolysis of coke. This study aims to analyze the relationship between the exposure of PAHs and the risk of genetic damages such as chromosomal alteration (CA), micronucleus (MN), and DNA damage (PCR-RFLP) in peripheral blood lymphocytes of 27 coke oven workers and equal number of control subjects. The exposed subjects and controls were divided into two groups based on their age (group Icoke oven workers under risk should be monitored for adverse effects of the any long-term exposure. PMID:24040626

  19. Problems in the fingerprints based polycyclic aromatic hydrocarbons source apportionment analysis and a practical solution.

    Science.gov (United States)

    Zou, Yonghong; Wang, Lixia; Christensen, Erik R

    2015-10-01

    This work intended to explain the challenges of the fingerprints based source apportionment method for polycyclic aromatic hydrocarbons (PAH) in the aquatic environment, and to illustrate a practical and robust solution. The PAH data detected in the sediment cores from the Illinois River provide the basis of this study. Principal component analysis (PCA) separates PAH compounds into two groups reflecting their possible airborne transport patterns; but it is not able to suggest specific sources. Not all positive matrix factorization (PMF) determined sources are distinguishable due to the variability of source fingerprints. However, they constitute useful suggestions for inputs for a Bayesian chemical mass balance (CMB) analysis. The Bayesian CMB analysis takes into account the measurement errors as well as the variations of source fingerprints, and provides a credible source apportionment. Major PAH sources for Illinois River sediments are traffic (35%), coke oven (24%), coal combustion (18%), and wood combustion (14%). PMID:26208321

  20. Distribution and sources of polycyclic aromatic hydrocarbons (PAHs) in street dust from the Tokyo Metropolitan area.

    Science.gov (United States)

    Takada, H; Onda, T; Harada, M; Ogura, N

    1991-09-01

    Molecular distributions of polycyclic aromatic hydrocarbons (PAHs) in street dust samples collected from the Tokyo Metropolitan area were determined by capillary gas chromatography following HPLC fractionation. Three- to six-ring PAHs and sulfur-heterocyclics were detected. PAHs in the dusts were dominated by three and four unsubstituted ring systems with significant amounts of their alkyl homologues. PAHs were widely distributed in the streets, with concentrations (sigma COMB) of a few microgram/g dust. Automobile exhaust, asphalt, gasoline fuel, diesel fuel, tyre particles, automobile crankcase oils, and atmospheric fallout were also analysed. The PAH profile, especially the relative abundance of alkyl-PAHs and sulfur-containing heterocyclics, indicated that PAHs in the street dusts from roads carrying heavy traffic are mainly derived from automobile exhausts; dusts from residential areas have a more significant contribution from atmospheric fallout.

  1. [Limit values for polycyclic aromatic hydrocarbons in soil of children's playgrounds--basic criteria and recommendations].

    Science.gov (United States)

    Roscher, E; Liebl, B; Schwegler, U; Schmied, R; Kerscher, G

    1996-01-01

    Elevated concentrations of polycyclic aromatic hydrocarbons (PAK) are often found in the soil of former waste disposal sites, industrial areas, etc. It is desirable and useful to determine orientation values to facilitate and unify the evaluation of contaminations under the aspects of present or planned uses of an area, health protection and decision-making on remedial measures. In the present paper we wish to draw attention to, and discuss problems resulting from, particular characteristics of PAK, e.g. the toxicological property "complete carcinogens" or the necessity of taking into account oral, inhalative and dermal exposure of children on a playground. Based on the discussion, orientation values for benzo[a]pyrene and PAK ("normal" pattern) of 0.5 mg/kg soil and 5 mg/kg soil, respectively, are recommended for top soil of vegetation-free playgrounds. In comparison, deductions carried out by other working groups are presented.

  2. A 25-year record of polycyclic aromatic hydrocarbons in soils amended with sewage sludges

    DEFF Research Database (Denmark)

    Lichtfouse, Eric; Sappin-Didier, Valérie; Denaix, Laurence;

    2005-01-01

    We studied polycyclic aromatic hydrocarbons (PAHs) in crop soils amended with 1000 tonnes dry weight of sewage sludges per 10,000 m(2) from 1974 to 1992, then after sludges addition from 1993 to 1999. The absence of variations of total PAHs levels of control soils, averaging at 123 mu g/Kg, shows...... the absence of horizontal contamination. During sludges addition, the total PAHs levels in amended soils increased from 232 to 402 mu g/Kg. Seven years after sludges addition, it decreased to 275 mu g/Kg, which is still more than twice the levels of control soils. This finding shows that sludges PAHs...... are preserved in crop soils for long periods of time, on a human scale....

  3. The phototoxicity of polycyclic aromatic hydrocarbons: a theoretical study of excited states and correlation to experiment.

    Science.gov (United States)

    Betowski, Leon D; Enlow, Mark; Riddick, Lee

    2002-06-01

    Investigators using models to determine the phototoxic effects of sunlight on polycyclic aromatic hydrocarbons (PAHs) have invoked the excited states of the molecule as important in elucidating the mechanism of these reactions. Energies of actual excited states were calculated for ten PAHs by several ab initio methods. The main method used for these calculations was the Configuration Interaction approach, modeling excited states as combinations of single substitutions out of the Hartree-Fock ground state. These calculations correlate well with both experimentally measured singlet and triplet state energies and also previous HOMO-LUMO gap energies that approximate the singlet state energies. The excited state calculations then correlate well with general models of photo-induced toxicity based for the PAHs.

  4. Analysis of carcinogenic Polycyclic Aromatic Hydrocarbons (PAHS): an overview of modern electroanalytical techniques and their applications.

    Science.gov (United States)

    Şentürk, Zühre

    2013-02-01

    A number of Polycyclic Aromatic Hydrocarbons (PAHs) have been shown to be toxicants, and induce carcinogenic and immunotoxic effects. Since PAHs are often present in low concentrations and it may be difficult to determine them in complex matrices, it is therefore essential to use powerful analytical tools to separate and identify the analyses in the samples. In this paper, initially, a short description of the principles, instrumentation, and use of common extraction and analytical techniques for PAH pollutants and their metabolites will be made in light of the previously reported works and major reviews. Special attention will be given to the use of modern polarographic and voltammetric techniques on the mercury and different types of solid electrodes, together with their some practical applications. The main drawbacks and limitations of these methods will also be discussed.

  5. Distribution and sources of polycyclic aromatic hydrocarbons (PAHs) in street dust from the Tokyo Metropolitan area.

    Science.gov (United States)

    Takada, H; Onda, T; Harada, M; Ogura, N

    1991-09-01

    Molecular distributions of polycyclic aromatic hydrocarbons (PAHs) in street dust samples collected from the Tokyo Metropolitan area were determined by capillary gas chromatography following HPLC fractionation. Three- to six-ring PAHs and sulfur-heterocyclics were detected. PAHs in the dusts were dominated by three and four unsubstituted ring systems with significant amounts of their alkyl homologues. PAHs were widely distributed in the streets, with concentrations (sigma COMB) of a few microgram/g dust. Automobile exhaust, asphalt, gasoline fuel, diesel fuel, tyre particles, automobile crankcase oils, and atmospheric fallout were also analysed. The PAH profile, especially the relative abundance of alkyl-PAHs and sulfur-containing heterocyclics, indicated that PAHs in the street dusts from roads carrying heavy traffic are mainly derived from automobile exhausts; dusts from residential areas have a more significant contribution from atmospheric fallout. PMID:1785054

  6. [Symptoms of atopy in persons exposed to chronic immunosuppression of polycyclic aromatic hydrocarbons].

    Science.gov (United States)

    Szczeklik, J; Kowalczyk, E; Gałuszka, Z

    1995-01-01

    The frequency of the atopy symptoms was estimated in 126 coke oven workers chronically exposed to polycyclic aromatic hydrocarbons (PAHs). The assessment was based on questionnaire, point skin tests with the allergens of dust, feathers, mould grass as well as on the measurements of total blood serum IgE concentration. The control group was consisted of 75 men, workers of cold rolling mill division where the environmental conditions were much better. It was observed that positive questionnaire data and positive skin tests were significantly less frequent in men exposed to PAHs. The men serum IgE values were not statistically different in both group workers although in coke oven workers the tendency to higher IgE values was observed. It is rather suggested that more useful method might be the measurement of specific serum IgE.

  7. Cyclodextrin-promoted Diels Alder reactions of a polycyclic aromatic hydrocarbon under mild reaction conditions

    Science.gov (United States)

    Chaudhuri, Sauradip; Phelan, Tyler; Levine, Mindy

    2015-01-01

    Reported herein is the effect of cyclodextrins on the rates of aqueous Diels Alder reactions of 9-anthracenemethanol with a variety of N-substituted maleimides. These reactions occurred under mild reaction conditions (aqueous solvent, 40 °C), and were most efficient for the reaction of N-cyclohexylmaleimide with a methyl-β-cyclodextrin additive (94% conversion in 24 hours). These results can be explained on the basis of a model wherein the cyclodextrins bind the hydrophobic substituents on the maleimides and activate the dienophile via electronic modulation of the maleimide double bond. The results reported herein represent a new mechanism for cyclodextrin-promoted Diels Alder reactions, and have significant potential applications in the development of other cyclodextrin-promoted organic transformations. Moreover, the ability to deplanarize polycyclic aromatic hydrocarbons (PAHs) under mild conditions, as demonstrated herein, has significant applications for PAH detoxification. PMID:26692588

  8. High-resolution IR absorption spectroscopy of polycyclic aromatic hydrocarbons: the realm of anharmonicity

    CERN Document Server

    Maltseva, Elena; Candian, Alessandra; Mackie, Cameron J; Huang, Xinchuan; Lee, Timothy J; Tielens, Alexander G G M; Oomens, Jos; Buma, Wybren Jan

    2015-01-01

    We report on an experimental and theoretical investigation of the importance of anharmonicity in the 3 micron CH stretching region of Polycyclic Aromatic Hydrocarbon (PAH) molecules. We present mass-resolved, high-resolution spectra of the gas-phase cold (~4K) linear PAH molecules naphthalene, anthracene, and tetracene. The measured IR spectra show a surprisingly high number of strong vibrational bands. For naphthalene, the observed bands are well separated and limited by the rotational contour, revealing the band symmetries. Comparisons are made to the harmonic and anharmonic approaches of the widely used Gaussian software. We also present calculated spectra of these acenes using the computational program SPECTRO, providing anharmonic predictions enhanced with a Fermi-resonance treatment that utilises intensity redistribution. We demonstrate that the anharmonicity of the investigated acenes is strong, dominated by Fermi resonances between the fundamental and double combination modes, with triple combination ...

  9. Development and certification of a coal fly ash certified reference material for selected polycyclic aromatic hydrocarbons.

    Science.gov (United States)

    Cao, X; Xu, X; Cui, W; Xi, Z

    2001-08-01

    The development and certification of a coal fly ash certified reference material (CRM) for polycyclic aromatic hydrocarbons (PAH) is described; this is the first natural matrix CRM for organic environmental analysis in China. The homogeneity and stability of this material have been tested by HPLC. The concentrations of several PAH were determined by use of two independent, different methods--solvent extraction-HPLC analysis with UV detection coupled with fluorescence detection (FLD) and solvent extraction, isolation with a silica column, and GC analysis with flame ionization detection (FID). Five certified values were determined: phenanthrene 7.1 +/- 2.6 microg g(-1), anthracene 2.0 +/- 0.8 microg g(-1), fluoranthene 7.4 +/- 1.9 microg g(-1), pyrene 7 +/- 2 microg g(-1), and benzo[a]pyrene 1.3 +/- 0.3 microg g(-1). Reference values for several other PAH are also suggested. PMID:11583083

  10. Diterpanes, triterpanes, steranes, and aromatic hydrocarbons in natural bitumens and pyrolysates from different humic coals

    Science.gov (United States)

    Lu, Shan-Tan; Kaplan, Isaac R.

    1992-07-01

    Data are presented on the distribution of diterpanes, triterpanes, steranes, and aromatic hydrocarbons in the natural bitumens extracted from unheated coals identified as Rocky Mountain coal (RMC), Australian Gippsland Latrobe Eocene coal (GEC), Australian Gippsland Latrobe Cretaceous coal (GCC), and Texas Wilcox lignite (WL), as well as from pyrolysates obtained from heating of these coals. It was found that pentacyclic triterpanes are dominant in GEC, GCC, and WL, whereas diterpanes strongly predominate in the bitumen of RMC, indicating that resin is a more important constituent of RMC than of the other coals and that it releases the diterpenoids at an early stage of diagenesis. It was also found that the composition of diterpanes is different among these coals and that the distributions of sterane and triterpane in the natural bitumen of coals are very different from those of pyrolysates.

  11. Artificial neural network for modeling the extraction of aromatic hydrocarbons from lube oil cuts

    Energy Technology Data Exchange (ETDEWEB)

    Mehrkesh, A.H.; Hajimirzaee, S. [Islamic Azad University, Majlesi Branch, Isfahan (Iran, Islamic Republic of); Hatamipour, M.S.; Tavakoli, T. [Department of Chemical Engineering, University of Isfahan, Isfahan (Iran, Islamic Republic of)

    2011-03-15

    An artificial neural network (ANN) approach was used to obtain a simulation model to predict the rotating disc contactor (RDC) performance during the extraction of aromatic hydrocarbons from lube oil cuts, to produce a lubricating base oil using furfural as solvent. The field data used for training the ANN model was obtained from a lubricating oil production company. The input parameters of the ANN model were the volumetric flow rates of feed and solvent, the temperatures of feed and solvent, and the disc rotation rate. The output parameters were the volumetric flow rate of the raffinate phase and the extraction yield. In this study, a feed-forward multi-layer perceptron neural network was successfully used to demonstrate the complex relationship between the mentioned input and output parameters. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  12. Toxicity assessment of polycyclic aromatic hydrocarbons in sediments from European high mountain lakes.

    Science.gov (United States)

    Quiroz, Roberto; Grimalt, Joan O; Fernández, Pilar

    2010-05-01

    Sediment quality guidelines and toxic equivalent factors have been used for assessment of the toxicity of sedimentary long-range atmospherically transported polycyclic aromatic hydrocarbons (PAHs) to the organisms living in high mountain European lakes. This method has provided indices that are consistent with experimental studies evaluating in situ sedimentary estrogenic activity or physiological response to AhR binding in fish from the same lakes. All examined lakes in north, central, west, northeast and southeast European mountains have shown sedimentary PAH concentrations that are above thresholds of no effect but only those situated in the southeast lakes district exhibited concentrations above the indices of probable effects. These mountains, Tatras, are also those having PAH concentrations of highest activity for AhR binding. Chrysene+triphenylene, dibenz[a]anthracene, benzo[k]fluoranthene and indeno[1,2,3-cd]pyrene are the main compounds responsible for the observed toxic effects.

  13. Inclusion of poly-aromatic hydrocarbon (PAH) molecules in a functionalized layered double hydroxide

    Indian Academy of Sciences (India)

    L Mohanambe; S Vasudevan

    2006-01-01

    The internal surface of an Mg-Al layered double hydroxide has been functionalized by anchoring carboxy-methyl derivatized -cyclodextrin cavities to the gallery walls. Neutral polyaromatic hydrocarbon (PAH) molecules have been included within the functionalized solid by driving the hydrophobic aromatic molecules from a polar solvent into the less polar interior of the anchored cyclodextrin cavities by a partitioning process. The optical (absorption and emission) properties of the PAH molecules included within the functionalized Mg-Al layered double hydroxide solid are similar to that of dilute solutions of the PAH in non-polar solvents. The unique feature of these hybrid materials is that they are thermally stable over a wide temperature range with their emission properties practically unaltered.

  14. A molecular dynamics study on slow ion interactions with the polycyclic aromatic hydrocarbon molecule anthracene

    International Nuclear Information System (INIS)

    Atomic collisions with polycyclic aromatic hydrocarbon (PAH) molecules are astrophysically particularly relevant for collision energies of less than 1 keV. In this regime, the interaction dynamics are dominated by elastic interactions. We have employed a molecular dynamics simulation based on analytical interaction potentials to model the interaction of low energy hydrogen and helium projectiles with isolated anthracene (C14H10) molecules. This approach allows for a very detailed investigation of the elastic interaction dynamics on an event by event basis. From the simulation data the threshold projectile kinetic energies above which direct C atom knock out sets in were determined. Anthracene differential energy transfer cross sections and total (dissociation) cross sections were computed for a wide range of projectile kinetic energies. The obtained results are interpreted in the context of PAH destruction in astrophysical environments.

  15. Selection of oxidant doses for in situ chemical oxidation of soils contaminated by polycyclic aromatic hydrocarbons (PAHs): A review.

    Science.gov (United States)

    Ranc, B; Faure, P; Croze, V; Simonnot, M O

    2016-07-15

    In situ chemical oxidation (ISCO) is a promising alternative to thermal desorption for the remediation of soils contaminated with organic compounds such as polycyclic aromatic hydrocarbons (PAHs). For field application, one major issue is the selection of the optimal doses of the oxidizing solution, i.e. the oxidant and appropriate catalysts and/or additives. Despite an extensive scientific literature on ISCO, this choice is very difficult because many parameters differ from one study to another. The present review identifies the critical factors that must be taken into account to enable comparison of these various contributions. For example, spiked soils and aged, polluted soils cannot be compared; PAHs freshly spiked into a soil are fully available for degradation unlike a complex mixture of pollutants trapped in a soil for many years. Another notable example is the high diversity of oxidation conditions employed during batch experiments, although these affect the representativeness of the system. Finally, in this review a methodology is also proposed based on a combination of the stoichiometric oxidant demand of the organic pollutants and the design of experiments (DOE) in order to allow a better comparison of the various studies so far reported. PMID:27043880

  16. Occurrence of polycyclic aromatic hydrocarbons below coal-tar-sealed parking lots and effects on stream benthic macroinvertebrate communities

    Energy Technology Data Exchange (ETDEWEB)

    Scoggins, M.; McClintock, N.L.; Gosselink, L.; Bryer, P. [City Austin, Austin, TX (United States)

    2007-12-15

    Parking-lot pavement sealants recently have been recognized as a major source of polycyclic aromatic hydrocarbons (PAHs) in urban stream sediments in Austin, Texas. Laboratory and field studies have shown that PAHs in sediments can be toxic to aquatic organisms and can degrade aquatic communities. After identifying increases in concentrations of PAHs in sediments below seal-coated parking lots, we investigated whether the increases had significant effects on stream biota in 5 Austin streams. We sampled sediment chemistry and biological communities above and below the point at which stormwater runoff from the parking lots discharged into the streams, thus providing 5 upstream reference sites and 5 downstream treatment sites. Differences between upstream and downstream concentrations of total PAH ranged from 3.9 to 32 mg/kg. Analysis of the species occurrence data from pool and riffle habitats indicated a significant decrease in community health at the downstream sites, including decreases in richness, intolerant taxa, Diptera taxa, and density. In pool sediments, Chironomidae density was negatively correlated with PAH concentrations, whereas Oligochaeta density responded positively to PAH concentrations. In general, pool taxa responded more strongly than riffle taxa to PAHs, but riffle taxa responded more broadly than pool taxa. Increases in PAH sediment-toxicity units between upstream and downstream sites explained decreases in taxon richness and density in pools between upstream and downstream sites.

  17. Polycyclic aromatic hydrocarbons (PAHs) in a large South American industrial coastal area (Santos Estuary, Southeastern Brazil): Sources and depositional history

    International Nuclear Information System (INIS)

    Highlights: → In early 1980s, Santos Estuary became known as one of the worst polluted in the world. → PAHs levels were similar to the values reported for marine sediments worldwide. → PAHs analyses indicated multiple sources of these compounds (oil and pyrolitic origin). → The decline of oil consumption due to the world oil crisis (late 1970s) was shown. → The input of organic pollutants is a historical problem for the Santos Estuary. - Abstract: Located in southeastern Brazil, the Santos Estuary has the most important industrial and urban population area of South America. Since the 1950's, increased urbanization and industrialization near the estuary margins has caused the degradation of mangroves and has increased the discharge of sewage and industrial effluents. The main objectives of this work were to determine the concentrations and sources of polycyclic aromatic hydrocarbons (PAHs) in sediment cores in order to investigate the input of these substances in the last 50 years. The PAHs analyses indicated multiple sources of these compounds (oil and pyrolitic origin), basically anthropogenic contributions from biomass, coal and fossil fuels combustion. The distribution of PAHs in the cores was associated with the formation and development of Cubatao industrial complex and the Santos harbour, waste disposal, world oil crisis and the pollution control program, which results in the decrease of organic pollutants input in this area.

  18. Effect of roasting conditions on the polycyclic aromatic hydrocarbon content in ground Arabica coffee and coffee brew.

    Science.gov (United States)

    Houessou, Justin Koffi; Maloug, Saber; Leveque, Anne-Sophie; Delteil, Corine; Heyd, Bertrand; Camel, Valérie

    2007-11-14

    Roasting is a critical process in coffee production as it enables the development of flavor and aroma. At the same time, roasting may lead to the formation of nondesirable compounds, such as polycyclic aromatic hydrocarbons (PAHs). In this study, Arabica green coffee beans from Cuba were roasted under controlled conditions to monitor PAH formation during the roasting process. Roasting was performed in a pilot spouted bed roaster, with the inlet air temperature varying from 180 to 260 degrees C, using both dark (20 min) and light (5 min) roasting conditions. Several PAHs were determined in both roasted coffee samples and green coffee samples. Also, coffee brews, obtained using an electric coffee maker, were analyzed for final estimation of PAH transfer coefficients to the infusion. Formation of phenanthrene, anthracene, and benzo[a]anthracene in coffee beans was observed at temperatures above 220 degrees C, whereas formation of pyrene and chrysene required 260 degrees C. Low levels of benzo[g,h,i]perylene were also noted for dark roasting under 260 degrees C, with simultaneous partial degradation of three-cycle PAHs, suggesting that transformation of low molecular PAHs to high molecular PAHs occurs as the roasting degree is increased. The PAH transfer to the infusion was quite moderate (<35%), with a slightly lower extractability for dark-roasted coffee as compared to light-roasted coffee. PMID:17941690

  19. Role of environmental factors and microorganisms in determining the fate of polycyclic aromatic hydrocarbons in the marine environment

    Science.gov (United States)

    Duran, Robert; Cravo-Laureau, Cristiana

    2016-01-01

    Polycyclic aromatic hydrocarbons (PAHs) are widespread in marine ecosystems and originate from natural sources and anthropogenic activities. PAHs enter the marine environment in two main ways, corresponding to chronic pollution or acute pollution by oil spills. The global PAH fluxes in marine environments are controlled by the microbial degradation and the biological pump, which plays a role in particle settling and in sequestration through bioaccumulation. Due to their low water solubility and hydrophobic nature, PAHs tightly adhere to sediments leading to accumulation in coastal and deep sediments. Microbial assemblages play an important role in determining the fate of PAHs in water and sediments, supporting the functioning of biogeochemical cycles and the microbial loop. This review summarises the knowledge recently acquired in terms of both chronic and acute PAH pollution. The importance of the microbial ecology in PAH-polluted marine ecosystems is highlighted as well as the importance of gaining further in-depth knowledge of the environmental services provided by microorganisms. PMID:27519427

  20. Methanogenic degradation of (amino)aromatic compounds by anaerobic microbial communities

    NARCIS (Netherlands)

    Linkova, Y.V.; Stams, A.J.M.

    2011-01-01

    Degradation of a range of aromatic substrates by anaerobic microbial communities was studied. Active methanogenic microbial communities decomposing aminoaromatic acids and azo dyes into CH4 and CO2 were isolated. Products of primary conversion were found to be 2-hydroxybenzyl and benzyl alcohols gra

  1. A novel cloud-point extraction process for preconcentrating selected polycyclic aromatic hydrocarbons in aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Bai, D.; Li, J.; Chen, S.B.; Chen, B.-H. [National University of Singapore (Singapore). Dept. of Chemical and Environmental Engineering

    2001-10-01

    Polycyclic aromatic hydrocarbons (PAHs) released in such processes as incomplete coal combustion and during the disposal of coal tar, are subject to strict emission controls in which the determination of PAHs has to be addressed. PAHs have low aqueous solubility which necessitates preconcentration prior to the analytical determination of PAHs. A novel but simple cloud-point extraction (CPE) process is developed to preconcentrate the trace of selected polycyclic aromatic hydrocarbons (PAHs) with the use of the readily biodegradable nonionic surfactant of secondary ethyoxylated alcohol Tergitol 15-S-7 as extractant. The concentrations of PAHs, mixtures of naphthalene and phenanthrene as well as pyrene in the spiked samples were determined with the new CPE process at ambient temperature (23{degree}C) followed by high performance liquid chromatography (HPLC) with fluorescence detection. More than 80% of phenanthrene and pyrene, respectively, and 96% of naphthalene initially present in the aqueous solutions with concentrations near or below their aqueous solubilities were recovered using this new CPE process. Importantly Tergitol 15-S-7 does not give any fluorometric signal to interfere with fluorescence detection of PAHs in the UV range. No special washing step is, thus, required to remove surfactant before HPLC analyses. Different experimental conditions were studied. The optimum conditions for the preconcentration and determination of these selected PAHs at ambient temperature have been established as the following: (1) 3 wt% surfactant; (2) addition of 0.5 M Na{sub 2}SO{sub 4}; (3) 10 min for equilibration time; and (4) 3000 rpm for centrifugal speed with duration of 10 min. 50 refs., 7 figs.

  2. Sedimentary record of polycyclic aromatic hydrocarbons in Lake Erhai,Southwest China

    Institute of Scientific and Technical Information of China (English)

    Jianyang Guo; Zhang Liang; Haiqing Liao; Zhi Tang; Xiaoli Zhao; Fengchang Wu

    2011-01-01

    The temporal distribution of polycyclic aromatic hydrocarbons (PAHs) was investigated in a sediment core from Lake Erhal in Southwest China using gas-chromatography/mass spectrometry (GC/MS) method.The total organic carbon (TOC) normalized total PAHs concentrations (sum of US Environmental Protection Agency proposed 16 priority PAHs) ranged from 31.9 to 269 μg/g dry weight (dw),and were characterized by a slowly increasing stage in the deeper sediments and a sharp increasing stage in the upper sediments.The PAHs in the sediments were dominated by low molecular weight (LMW) PAHs,suggesting that the primary source of PAHs was low- and moderate temperature combustion processes.However,both the significant increase in high molecular weight (HMW) PAHs in the upper sediments and the vertical profile of diagnostic ratios pointed out a change in the sources of PAHs from low-temperature combustion to high-temperature combustion.The ecotoxicological assessment based on consensus-based sediment quality guidelines implied that potential adverse biological impacts were possible for benzo(ghi)perylenelene and most LMW PAHs.In addition,the total BaP equivalent quotient of seven carcinogenic polycyclic aromatic hydrocarbons (BaA,CHr,BbF,BkF,BaP,DBA and INP) was 106.1 ng/g,according to the toxic equivalency factors.Although there was no great biological impact associated with the HMW PAlls,great attention should be paid to these PAH components based on their rapid increase in the upper sediments.

  3. [Improving Agricultural Safety of Soils Contaminated with Polycyclic Aromatic Hydrocarbons by In Situ Bioremediation].

    Science.gov (United States)

    Jiao, Hai-huan; Pan, Jian-gang; Xu, Shena-jun; Bai, Zhi-hui; Wang, Dong; Huang, Zhan-bin

    2015-08-01

    In order to reduce the risk of enrichment of polycyclic aromatic hydrocarbons (PAHs) in crops, reduce the potential hazards of food-sourced PAHs to human and increase the agricultural safety of PAHs contaminated soils, the bio-augmented removal of polycyclic aromatic hydrocarbons (PAHs) was investigated through in situ remediation by introducing Rhodobacter sphaeroides (RS) into the agricultural soil contaminated by PAHs. The 50-times diluted RS was sprayed on leaf surface (in area B) or irrigated to roots (in area D). The treatment of spraying water of the equal amount was taken as the control (A) and the wheat field without any treatment as the blank (CK). Treatments were conducted since wheat seeding. Soil and wheat samples were collected in the mature period to analyze the changes of community structure of the soil microorganisms and the concentration of PAHs in soils and investigate the strengthening and restoration effects of RS on PAHs contaminated soils. Compared to the CK Area, the areas B and D revealed that the variation ratio of phospholipid fatty acids (PLFAs) that were the biomarker of soil microorganisms was 29.6%, and the ratio of total PAHs removed was increased 1.59 times and 1.68 times, respectively. The dry weight of wheat grain of 50 spikes was increased by 8.95% and 12.5%, respectively, and the enrichment factor of total PAHs was decreased by 58.9% and 62.2% respectively in the wheat grains. All the results suggested that RS reduced enrichment of PAHs in wheat grains and increased wheat yield, which had great exploitation and utilization potentiality in repairing and improving the agricultural safety of the soils contaminated with PHAs.

  4. Biodiesel presence in the source zone hinders aromatic hydrocarbons attenuation in a B20-contaminated groundwater

    Science.gov (United States)

    Ramos, Débora Toledo; Lazzarin, Helen Simone Chiaranda; Alvarez, Pedro J. J.; Vogel, Timothy M.; Fernandes, Marilda; do Rosário, Mário; Corseuil, Henry Xavier

    2016-10-01

    The behavior of biodiesel blend spills have received limited attention in spite of the increasing and widespread introduction of biodiesel to the transportation fuel matrix. In this work, a controlled field release of biodiesel B20 (100 L of 20:80 v/v soybean biodiesel and diesel) was monitored over 6.2 years to assess the behavior and natural attenuation of constituents of major concern (e.g., BTEX (benzene, toluene, ethyl-benzene and xylenes) and PAHs (polycyclic aromatic hydrocarbons)) in a sandy aquifer material. Biodiesel was preferentially biodegraded compared to diesel aromatic compounds with a concomitant increase in acetate, methane (near saturation limit (≈ 22 mg L- 1)) and dissolved BTEX and PAH concentrations in the source zone during the first 1.5 to 2.0 years after the release. Benzene and benzo(a)pyrene concentrations remained above regulatory limits in the source zone until the end of the experiment (6.2 years after the release). Compared to a previous adjacent 100-L release of ethanol-amended gasoline, biodiesel/diesel blend release resulted in a shorter BTEX plume, but with higher residual dissolved hydrocarbon concentrations near the source zone. This was attributed to greater persistence of viscous (and less mobile) biodiesel than the highly-soluble and mobile ethanol in the source zone. This persistence of biodiesel/diesel NAPL at the source zone slowed BTEX and PAH biodegradation (by the establishment of an anaerobic zone) but reduced the plume length by reducing mobility. This is the first field study to assess biodiesel/diesel blend (B20) behavior in groundwater and its effects on the biodegradation and plume length of priority groundwater pollutants.

  5. The C--H Stretching Features at 3.2--3.5 Micrometer of Polycyclic Aromatic Hydrocarbons with Aliphatic Sidegroups

    CERN Document Server

    Yang, Xuejuan; Glaser, Rainer; Zhong, Jianxin

    2016-01-01

    The so-called unidentified infrared emission (UIE) features at 3.3, 6.2, 7.7, 8.6, and 11.3 micrometer are ubiquitously seen in a wide variety of astrophysical regions. The UIE features are characteristic of the stretching and bending vibrations of aromatic hydrocarbon materials, e.g., polycyclic aromatic hydrocarbon (PAH) molecules. The 3.3 micrometer aromatic C--H stretching feature is often accompanied by a weaker feature at 3.4 micrometer. The latter is often thought to result from the C--H stretch of aliphatic groups attached to the aromatic systems. The ratio of the observed intensity of the 3.3 micrometer aromatic C--H feature to that of the 3.4 micrometer aliphatic C--H feature allows one to estimate the aliphatic fraction of the UIE carriers, provided that the intrinsic oscillator strengths of the 3.3 micrometer aromatic C--H stretch (A3.3) and the 3.4 micrometer aliphatic C--H stretch (A3.4) are known. While previous studies on the aliphatic fraction of the UIE carriers were mostly based on the A3.4...

  6. Removal of polycyclic aromatic hydrocarbons from organic solvents by ashes wastes

    International Nuclear Information System (INIS)

    Polycyclic aromatic hydrocarbons (PAHs) can be formed during the refinery processes of crude petroleum. Their removal is of great importance. The same happens with other organic solvents used for the extraction of PAHs (hexane, acetonitrile...), which can be polluted with PAHs. Kinetic and equilibrium batch sorption tests were used to investigate the effect of wood ashes wastes as compared to activated carbon on the sorption of three representative PAHs from n-hexane and acetonitrile. Mussel shell ashes were discarded for batch sorption experiments because they were the only ashes containing PAHs. The equilibrium time was reached at 16 h. Physical sorption caused by the aromatic nature of the compounds was the main mechanism that governed the PAHs removal process. Our investigation revealed that wood ashes obtained at lower temperature (300 deg. C) did not show any PAHs sorption, while ashes obtained at higher temperature (>500 deg. C) have adsorbent sites readily available for the PAH molecules. An increase in the molecular weight of PAHs has a strong effect on sorption wood ashes wastes. As low the wood ashes particle size as high the sorption of PAHs, as a result of differences in adsorbent sites. The performance of wood ash wastes vs. activated carbon to remove 10 PAHs from organic solvents is competitive in price, and a good way for waste disposal.

  7. Physico-chemical properties and toxicity of alkylated polycyclic aromatic hydrocarbons.

    Science.gov (United States)

    Kang, Hyun-Joong; Lee, So-Young; Kwon, Jung-Hwan

    2016-07-15

    Crude oil and refined petroleum products contain many polycyclic and heterocyclic aromatic hydrocarbons, in particular, alkylated PAHs. Although alkylated PAHs are found in significantly higher quantities than their corresponding unsubstituted PAHs, the most studies on the physico-chemical properties and toxicities of these compounds have been conducted on unsubstituted PAHs. In this study, we measured crucial physico-chemical properties (i.e., water solubility, partition coefficients between polydimethylsiloxane and water (KPDMSw), and partition coefficient between liposomes and water (Klipw)) of selected alkylated PAHs, and evaluated their toxicity using the luminescence inhibition of Aliivibrio fischeri and growth inhibition of Raphidocelis subcapitata. In general, the logarithms of these properties for alkylated PAHs showed good linear correlations with log Kow, as did those for unsubstituted PAHs. Changes in molecular symmetry on the introduction of alkyl groups on aromatic ring structure significantly altered water solubility. The inhibition of bacterial luminescence and algal growth by alkylated PAHs can be explained well by the baseline toxicity hypothesis, and good linear relationships between log Kow or log Klipw and log (1/EC50) were found.

  8. Polycyclic Aromatic Hydrocarbons and Breast Cancer: A Review of the Literature.

    Science.gov (United States)

    Korsh, Jessica; Shen, Allison; Aliano, Kristen; Davenport, Thomas

    2015-10-01

    Polycyclic aromatic hydrocarbons (PAHs) exist and persist in the atmosphere due to the incomplete combustion of fossil fuels, and are established human carcinogens. The influence of PAHs on the development of breast cancer, the most commonly diagnosed cancer in women worldwide, remains unclear. As established risk factors only account for approximately 41% of the breast cancer cases in the USA, researchers have sought to uncover environmental factors involved in breast cancer development. The breasts are particularly susceptible to aromatic carcinogenesis, and the implementation of biomarkers has provided promising insights regarding PAH-DNA adducts in breast cancer. The use of biomarkers measuring PAH-DNA adducts assesses exposure to eliminate the bias inherent in self-reporting measures in case-control studies investigating the link between PAHs and cancer. Adduct levels reflect exposure dose as well as how the body responds to this exposure, which is partially attributable to genetic variability. Evidence suggests that exposure to PAHs has a causational effect on breast cancer in humans, yet this interaction is not clearly understood. In vitro and animal-based studies have consistently revealed that exposure to PAHs deleteriously affects breast tissue, but there is no definitive link between these compounds and breast cancer. PMID:26688678

  9. Tumour-promoting activity of polycyclic aromatic hydrocarbons and their oxygenated or nitrated derivatives.

    Science.gov (United States)

    Misaki, Kentaro; Takamura-Enya, Takeji; Ogawa, Hideoki; Takamori, Kenji; Yanagida, Mitsuaki

    2016-03-01

    Various types of polycyclic aromatic compounds (PACs) in diesel exhaust particles are thought to contribute to carcinogenesis in mammals. Although the carcinogenicity, mutagenicity and tumour-initiating activity of these compounds have been evaluated, their tumour-promoting activity is unclear. In the present study, to determine the tumour-inducing activity of PACs, including previously known mutagenic compounds in atmospheric environments, a transformation assay for promoting activity mediated by the release of contact inhibition was conducted for six polycyclic aromatic hydrocarbons (PAHs), seven oxygenated PAHs (oxy-PAHs) and seven nitrated PAHs (nitro-PAHs) using mouse embryonic fibroblast cells transfected with the v-Ha-ras gene (Bhas 42 cells). Of these, two PAHs [benzo[k]fluoranthene (B[k]FA) and benzo[b]fluoranthene (B[b]FA)], one oxy-PAH [6H-benzo[cd]pyren-6-one (BPO)] and two nitro-PAHs (3-nitro-7H-benz[de]anthracen-7-one and 6-nitrochrysene) were found to exhibit particularly powerful tumour-promoting activity (≥10 foci following exposure to BPO). Further, an HO-1 antioxidant response activation was observed following exposure to B[k]FA, B[b]FA and BPO, suggesting that the induction of tumour-promoting activity in these compounds is correlated with the dysfunction of signal transduction via AhR-mediated responses and/or oxidative stress responses.

  10. High-Resolution IR Absorption Spectroscopy of Polycyclic Aromatic Hydrocarbons: The Realm of Anharmonicity

    Science.gov (United States)

    Maltseva, Elena; Petrignani, Annemieke; Candian, Alessandra; Mackie, Cameron J.; Huang, Xinchuan; Lee, Timothy J.; Tielens, Alexander G. G. M.; Oomens, Jos; Buma, Wybren Jan

    2016-01-01

    We report on an experimental and theoretical investigation of the importance of anharmonicity in the 3 micrometers CH stretching region of Polycyclic Aromatic Hydrocarbon (PAH) molecules. We present mass-resolved, high-resolution spectra of the gas-phase cold ((is) approximately 4K) linear PAH molecules naphthalene, anthracene, and tetracene. The measured IR spectra show a surprisingly high number of strong vibrational bands. For naphthalene, the observed bands are well separated and limited by the rotational contour, revealing the band symmetries. Comparisons are made to the harmonic and anharmonic approaches of the widely used Gaussian software. We also present calculated spectra of these acenes using the computational program SPECTRO, providing anharmonic predictions enhanced with a Fermi-resonance treatment that utilizes intensity redistribution. We demonstrate that the anharmonicity of the investigated acenes is strong, dominated by Fermi resonances between the fundamental and double combination modes, with triple combination bands as possible candidates to resolve remaining discrepancies. The anharmonic spectra as calculated with SPECTRO lead to predictions of the main modes that fall within 0.5% of the experimental frequencies. The implications for the Aromatic Infrared Bands, specifically the 3-m band are discussed.

  11. Polycyclic aromatic hydrocarbons in sediments and mussels of the western Mediterranean Sea

    Energy Technology Data Exchange (ETDEWEB)

    Baumard, P.; Budzinski, H.; Garrigues, P. [Univ. Bordeaux I, Talence (France)

    1998-05-01

    The distribution of polycyclic aromatic hydrocarbons (PAHs) has been investigated in superficial sediments and mussels (Mytilus galloprovincialis) of the western Mediterranean sea. The analyses were performed by gas chromatography coupled to mass spectrometry (GC-MS). The PAH concentrations ranged from 1 to 20,500 ng/g in the sediments. Different molecular indices allowed differentiation between the different pollutant sources. On the French coast, PAHs originated mainly from incomplete combustion of organic matter (pyrolytic origin), whereas for some sites in Corsica and Sardinia an overimposition of petrogenic PAHs occurred. The mussel PAH concentrations ranged from 25 to 390 ng/g. The total and individual PAH bioaccumulation factors were calculated. The correlation between sediment and mussel PAH content was discussed in terms of bioavailability. It was possible to distinguish different absorption routes for the xenobiotics according to their physicochemical properties. Because the mussel distribution of phenanthrene and anthracene seems to be governed by their water solubility, these compounds were probably mainly absorbed as the water-dissolved form, whereas the heavier molecular weight PAHs (more than four aromatic rings), whose sediment and mussel concentrations are correlated with higher correlation coefficients than for phenanthrene and anthracene, were probably mainly absorbed as adsorbed on particles. Furthermore, a possible preferential biotransformation of benzo[a]pyrene over benzo[e]pyrene is discussed.

  12. Polycyclic aromatic hydrocarbons (PAH) formation from the pyrolysis of different municipal solid waste fractions

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Hui [Key Laboratory for Thermal Science and Power Engineering of Ministry of Education, Department of Thermal Engineering, Tsinghua University, Beijing 100084 (China); Energy Research Institute, University of Leeds, Leeds LS2 9JT (United Kingdom); Wu, Chunfei, E-mail: c.wu@leeds.ac.uk [Energy Research Institute, University of Leeds, Leeds LS2 9JT (United Kingdom); Onwudili, Jude A. [Energy Research Institute, University of Leeds, Leeds LS2 9JT (United Kingdom); Meng, Aihong [Key Laboratory for Thermal Science and Power Engineering of Ministry of Education, Department of Thermal Engineering, Tsinghua University, Beijing 100084 (China); Zhang, Yanguo, E-mail: zhangyg@tsinghua.edu.cn [Key Laboratory for Thermal Science and Power Engineering of Ministry of Education, Department of Thermal Engineering, Tsinghua University, Beijing 100084 (China); Williams, Paul T., E-mail: p.t.williams@leeds.ac.uk [Energy Research Institute, University of Leeds, Leeds LS2 9JT (United Kingdom)

    2015-02-15

    Highlights: • PAH from pyrolysis of 9 MSW fractions was investigated. • Pyrolysis of plastics released more PAH than that of biomass. • Naphthalene was the most abundant PAH in the tar. • The mechanism of PAH release from biomass and plastics was proposed. - Abstract: The formation of 2–4 ring polycyclic aromatic hydrocarbons (PAH) from the pyrolysis of nine different municipal solid waste fractions (xylan, cellulose, lignin, pectin, starch, polyethylene (PE), polystyrene (PS), polyvinyl chloride (PVC), and polyethylene terephthalate (PET)) were investigated in a fixed bed furnace at 800 °C. The mass distribution of pyrolysis was also reported. The results showed that PS generated the most total PAH, followed by PVC, PET, and lignin. More PAH were detected from the pyrolysis of plastics than the pyrolysis of biomass. In the biomass group, lignin generated more PAH than others. Naphthalene was the most abundant PAH, and the amount of 1-methynaphthalene and 2-methynaphthalene was also notable. Phenanthrene and fluorene were the most abundant 3-ring PAH, while benzo[a]anthracene and chrysene were notable in the tar of PS, PVC, and PET. 2-ring PAH dominated all tar samples, and varied from 40 wt.% to 70 wt.%. For PS, PET and lignin, PAH may be generated directly from the aromatic structure of the feedstock.

  13. Random mixtures of polycyclic aromatic hydrocarbon spectra match interstellar infrared emission

    CERN Document Server

    Rosenberg, Marissa J F; Boersma, Christiaan

    2014-01-01

    The mid-infrared (IR; 5-15~$\\mu$m) spectrum of a wide variety of astronomical objects exhibits a set of broad emission features at 6.2, 7.7, 8.6, 11.3 and 12.7 $\\mu$m. About 30 years ago it was proposed that these signatures are due to emission from a family of UV heated nanometer-sized carbonaceous molecules known as polycyclic aromatic hydrocarbons (PAHs), causing them to be referred to as aromatic IR bands (AIBs). Today, the acceptance of the PAH model is far from settled, as the identification of a single PAH in space has not yet been successful and physically relevant theoretical models involving ``true'' PAH cross sections do not reproduce the AIBs in detail. In this paper, we use the NASA Ames PAH IR Spectroscopic Database, which contains over 500 quantum-computed spectra, in conjunction with a simple emission model, to show that the spectrum produced by any random mixture of at least 30 PAHs converges to the same 'kernel'-spectrum. This kernel-spectrum captures the essence of the PAH emission spectrum...

  14. Physico-chemical properties and toxicity of alkylated polycyclic aromatic hydrocarbons.

    Science.gov (United States)

    Kang, Hyun-Joong; Lee, So-Young; Kwon, Jung-Hwan

    2016-07-15

    Crude oil and refined petroleum products contain many polycyclic and heterocyclic aromatic hydrocarbons, in particular, alkylated PAHs. Although alkylated PAHs are found in significantly higher quantities than their corresponding unsubstituted PAHs, the most studies on the physico-chemical properties and toxicities of these compounds have been conducted on unsubstituted PAHs. In this study, we measured crucial physico-chemical properties (i.e., water solubility, partition coefficients between polydimethylsiloxane and water (KPDMSw), and partition coefficient between liposomes and water (Klipw)) of selected alkylated PAHs, and evaluated their toxicity using the luminescence inhibition of Aliivibrio fischeri and growth inhibition of Raphidocelis subcapitata. In general, the logarithms of these properties for alkylated PAHs showed good linear correlations with log Kow, as did those for unsubstituted PAHs. Changes in molecular symmetry on the introduction of alkyl groups on aromatic ring structure significantly altered water solubility. The inhibition of bacterial luminescence and algal growth by alkylated PAHs can be explained well by the baseline toxicity hypothesis, and good linear relationships between log Kow or log Klipw and log (1/EC50) were found. PMID:27037474

  15. Phototoxicity of individual polycyclic aromatic hydrocarbons and petroleum to marine invertebrate larvae and juveniles

    International Nuclear Information System (INIS)

    Phototoxicity resulting from photoactivated polycyclic aromatic hydrocarbons (PAHs) has been reported in the literature for a variety of freshwater organisms. The magnitude of increase in PAH toxicity often exceeds a factor of 100. In the marine environment phototoxicity to marine organisms has not been reported for individual or complex mixtures of PAHs. In this study, larvae and juveniles of the bivalve, Mulinia lateralis, and juveniles of the mysid shrimp, Mysidopsis bahia, were exposed to individual known phototoxic PAHs (anthracene, fluoranthene, pyrene), as well as the water-accommodated fractions of several petroleum products (Fuel Oil number-sign 2, Arabian Light Crude, Prudhoe Bay Crude, Fuel Oil number-sign 6) containing PAHs. Phototoxicity of individual PAHs was 12 to >50,000 times that of conventional toxicity. Three of the petroleum products demonstrated phototoxicity while the lightest product, Fuel Oil number-sign 2, was not phototoxic at the concentrations tested. The phototoxicity of petroleum products appears to be dependent on the composition and concentrations of phototoxic PAHs present: lighter oils have fewer multiple aromatic ring, phototoxic compounds while heavier oils have higher levels of these types of molecules. This study shows that phototoxicity can occur in marine waters to marine species. Further, the occurrence of oil in marine waters presents the additional risk of phototoxicity not routinely assessed for during oil spills

  16. Release behavior and formation mechanism of polycyclic aromatic hydrocarbons during coal pyrolysis.

    Science.gov (United States)

    Gao, Meiqi; Wang, Yulong; Dong, Jie; Li, Fan; Xie, Kechang

    2016-09-01

    Polycyclic aromatic hydrocarbons (PAHs) are major environmental pollutants. They have attracted considerable attention due to their severe potential carcinogenic, mutagenic and genotoxic effects on human health. In this study, five different rank coals from China were pyrolyzed using pyro-probe CDS 5250 and the release behavior of 16 PAHs under different pyrolysis conditions were studied by Gas Chromatography-Mass Spectrometer (GC-MS). The structural characteristics of the five coals were determined by Cross-Polarization/Magic Angle Spinning Carbon-13 Nuclear Magnetic Resonance (CP/MAS (13)C NMR) spectroscopy, and then the factors influencing the formation of PAHs during coal pyrolysis were discussed together with the coal structural data. It was shown that the amount of PAHs generated during coal pyrolysis was largely related to coal rank and followed the order of medium metamorphic coal > low metamorphic coal > high metamorphic coal. The amount of total PAHs varied as the temperature was increased from 400 °C to 1200 °C, which showed a trend of first increasing and then decreasing, with the maximum value at 800 °C. Moreover, the species of PAHs released varied with pyrolysis temperatures. When the temperature was lower than 800 °C, the small ring PAHs were the most abundant, while the proportion of heavy rings increased at higher temperature. The results indicate that the formation of PAHs during coal pyrolysis depends on the structure of the coal. The species and amounts of PAHs generated during coal pyrolysis are closely related to the contents of protonated aromatic carbons and bridging ring junction aromatic carbons present in the coal structure. PMID:27239965

  17. Release behavior and formation mechanism of polycyclic aromatic hydrocarbons during coal pyrolysis.

    Science.gov (United States)

    Gao, Meiqi; Wang, Yulong; Dong, Jie; Li, Fan; Xie, Kechang

    2016-09-01

    Polycyclic aromatic hydrocarbons (PAHs) are major environmental pollutants. They have attracted considerable attention due to their severe potential carcinogenic, mutagenic and genotoxic effects on human health. In this study, five different rank coals from China were pyrolyzed using pyro-probe CDS 5250 and the release behavior of 16 PAHs under different pyrolysis conditions were studied by Gas Chromatography-Mass Spectrometer (GC-MS). The structural characteristics of the five coals were determined by Cross-Polarization/Magic Angle Spinning Carbon-13 Nuclear Magnetic Resonance (CP/MAS (13)C NMR) spectroscopy, and then the factors influencing the formation of PAHs during coal pyrolysis were discussed together with the coal structural data. It was shown that the amount of PAHs generated during coal pyrolysis was largely related to coal rank and followed the order of medium metamorphic coal > low metamorphic coal > high metamorphic coal. The amount of total PAHs varied as the temperature was increased from 400 °C to 1200 °C, which showed a trend of first increasing and then decreasing, with the maximum value at 800 °C. Moreover, the species of PAHs released varied with pyrolysis temperatures. When the temperature was lower than 800 °C, the small ring PAHs were the most abundant, while the proportion of heavy rings increased at higher temperature. The results indicate that the formation of PAHs during coal pyrolysis depends on the structure of the coal. The species and amounts of PAHs generated during coal pyrolysis are closely related to the contents of protonated aromatic carbons and bridging ring junction aromatic carbons present in the coal structure.

  18. CHARACTERIZING THE INFRARED SPECTRA OF SMALL, NEUTRAL, FULLY DEHYDROGENATED POLYCYCLIC AROMATIC HYDROCARBONS

    Energy Technology Data Exchange (ETDEWEB)

    Mackie, C. J.; Peeters, E.; Cami, J. [Department of Physics and Astronomy, University of Western Ontario, London, ON N6A 3K7 (Canada); Bauschlicher, C. W. Jr., E-mail: mackie@strw.leidenuniv.nl [NASA Ames Research Center, MS 245-6, Moffett Field, CA 94035 (United States)

    2015-02-01

    We present the results of a computational study to investigate the infrared spectroscopic properties of a large number of polycyclic aromatic hydrocarbon (PAH) molecules and their fully dehydrogenated counterparts. We constructed a database of fully optimized geometries for PAHs that is complete for eight or fewer fused benzene rings, thus containing 1550 PAHs and 805 fully dehydrogenated aromatics. A large fraction of the species in our database have clearly non-planar or curved geometries. For each species, we determined the frequencies and intensities of their normal modes using density functional theory calculations. Whereas most PAH spectra are fairly similar, the spectra of fully dehydrogenated aromatics are much more diverse. Nevertheless, these fully dehydrogenated species show characteristic emission features at 5.2 μm, 5.5 μm, and 10.6 μm; at longer wavelengths, there is a forest of emission features in the 16-30 μm range that appears as a structured continuum, but with a clear peak centered around 19 μm. We searched for these features in Spitzer-IRS spectra of various positions in the reflection nebula NGC 7023. We find a weak emission feature at 10.68 μm in all positions except that closest to the central star. We also find evidence for a weak 19 μm feature at all positions that is not likely due to C{sub 60}. We interpret these features as tentative evidence for the presence of a small population of fully dehydrogenated PAHs, and discuss our results in the framework of PAH photolysis and the formation of fullerenes.

  19. Determining produced water originating polycyclic aromatic hydrocarbons in North Sea waters: comparison of sampling techniques

    International Nuclear Information System (INIS)

    A field study was carried out in the Norwegian sector of the North Sea during May and June 1997. The purpose was to measure the concentration of produced water originating polycyclic aromatic hydrocarbons (PAH) in seawater and to compare different sampling techniques for use in future monitoring programs. Three methods were used for direct water sampling: (1) in situ large volume sampling of particulate and dissolved hydrocarbons onto filters and XAD resins, (2) solid phase extraction (SPE) using polystyrene-divinylbenzene disks, (3) whole bulk water sampling. In addition, sampling by semi-permeable membrane devices (SPMDs) and blue mussels (Mytilus edulis) was used to obtain a 4 weeks average of the concentration of the target compounds in seawater. The samples were processed and analysed by GC-MS for determination of PAH concentrations. The measured concentrations were generally found to be low, and in many cases below the limits of detection. The comparison of sampling techniques showed that blue mussels and SPMDs are suitable for measuring PAH in both near-and far-field seawater. In situ large volume water sampling was also suitable for a wide range of PAH concentrations, but this technique was limited by high break-through of the low-molecular weight compounds, such as naphthalenes. The small sampling volumes limited the SPE and whole water sampling techniques, resulting in potential detection limit problems These grab-sampling techniques may, however, be suitable for monitoring in the near-field areas around the platforms. (Author)

  20. LABORATORY INVESTIGATIONS OF POLYCYCLIC AROMATIC HYDROCARBON FORMATION AND DESTRUCTION IN THE CIRCUMSTELLAR OUTFLOWS OF CARBON STARS

    Energy Technology Data Exchange (ETDEWEB)

    Contreras, Cesar S.; Salama, Farid, E-mail: cesar.contreras@nasa.gov, E-mail: Farid.Salama@nasa.gov [Space Science and Astrobiology Division, NASA-Ames Research Center, Moffett Field, CA 94035 (United States)

    2013-09-15

    The formation and destruction mechanisms of interstellar dust analogs formed from a variety of polycyclic aromatic hydrocarbon (PAH) and hydrocarbon molecular precursors are studied in the laboratory. We used the newly developed facility COSmIC, which simulates interstellar and circumstellar environments, to investigate both PAHs and species that include the cosmically abundant atoms O, N, and S. The species generated in a discharge plasma are detected, monitored, and characterized in situ using highly sensitive techniques that provide both spectral and ion mass information. We report here the first series of measurements obtained in these experiments which focus on the characterization of the most efficient molecular precursors in the chemical pathways that eventually lead to the formation of carbonaceous grains in the stellar envelopes of carbon stars. We compare and discuss the relative efficiencies of the various molecular precursors that lead to the formation of the building blocks of carbon grains. We discuss the most probable molecular precursors in terms of size and structure and the implications for the expected growth and destruction processes of interstellar carbonaceous dust.

  1. Does chemically dispersing crude oil increase the exposure of fish to polynuclear aromatic hydrocarbons (PAH)?

    Energy Technology Data Exchange (ETDEWEB)

    Ramachandran, S.D.; Khan, C.W.; Hodson, P.V. [Queen' s Univ., Kingston, ON (Canada). Dept. of Biology; Lee, K. [Department of Fisheries and Oceans, Dartmouth, NS (Canada). Bedford Inst. of Oceanography

    2002-07-01

    Dispersants or surfactants are often used to clean up oil spills on water to minimize the impact of oil pollution. Their use as an oil spill countermeasure, however, is controversial because the risk of ecological effects depends on whether the dispersant increases or decreases the exposure of aquatic species to the toxic components of oil. This study involved the measurement of CYP1A induction and bile metabolites of polycyclic aromatic hydrocarbons (PAH) in trout exposed to Corexit 9500 dispersant, water accommodated fractions, and chemically enhanced water accommodated fractions of 3 crude oils. The objective was to see if fish are exposed to more PAH in dispersed oil compared to equivalent amounts of water accommodated fraction. Preliminary results indicated 10 times higher induction in fish exposed to chemically enhanced water accommodated fraction compared to water accommodated fractions. The dispersed oil in water had higher concentrations of alkylated PAH compared to the water accommodated fraction. As hydrocarbon concentrations increased, the trend for medaka embryos was first to hatch earlier, then have mild edema, followed by severe edema and finally mortality.

  2. Assessing the Ecological Risk of Polycyclic Aromatic Hydrocarbons in Sediments at Langkawi Island, Malaysia

    Directory of Open Access Journals (Sweden)

    Essam Nasher

    2013-01-01

    Full Text Available Tourism-related activities such as the heavy use of boats for transportation are a significant source of petroleum hydrocarbons that may harm the ecosystem of Langkawi Island. The contamination and toxicity levels of polycyclic aromatic hydrocarbon (PAH in the sediments of Langkawi were evaluated using sediment quality guidelines (SQGs and toxic equivalent factors. Ten samples were collected from jetties and fish farms around the island in December 2010. A gas chromatography/flame ionization detector (GC/FID was used to analyse the 18 PAHs. The concentration of total PAHs was found to range from 869 ± 00 to 1637 ± 20 ng g−1 with a mean concentration of 1167.00 ± 24 ng g−1, lower than the SQG effects range-low (3442 ng g−1. The results indicated that PAHs may not cause acute biological damage. Diagnostic ratios and principal component analysis suggested that the PAHs were likely to originate from pyrogenic and petrogenic sources. The toxic equivalent concentrations of the PAHs ranged from 76.3 to 177 ng TEQ/g d.w., which is lower compared to similar studies. The results of mean effects range-median quotient of the PAHs were lower than 0.1, which indicate an 11% probability of toxicity effect. Hence, the sampling sites were determined to be the low-priority sites.

  3. Assessing the ecological risk of polycyclic aromatic hydrocarbons in sediments at Langkawi Island, Malaysia.

    Science.gov (United States)

    Nasher, Essam; Heng, Lee Yook; Zakaria, Zuriati; Surif, Salmijah

    2013-01-01

    Tourism-related activities such as the heavy use of boats for transportation are a significant source of petroleum hydrocarbons that may harm the ecosystem of Langkawi Island. The contamination and toxicity levels of polycyclic aromatic hydrocarbon (PAH) in the sediments of Langkawi were evaluated using sediment quality guidelines (SQGs) and toxic equivalent factors. Ten samples were collected from jetties and fish farms around the island in December 2010. A gas chromatography/flame ionization detector (GC/FID) was used to analyse the 18 PAHs. The concentration of total PAHs was found to range from 869 ± 00 to 1637 ± 20 ng g⁻¹ with a mean concentration of 1167.00 ± 24 ng g⁻¹, lower than the SQG effects range-low (3442 ng g⁻¹). The results indicated that PAHs may not cause acute biological damage. Diagnostic ratios and principal component analysis suggested that the PAHs were likely to originate from pyrogenic and petrogenic sources. The toxic equivalent concentrations of the PAHs ranged from 76.3 to 177 ng TEQ/g d.w., which is lower compared to similar studies. The results of mean effects range-median quotient of the PAHs were lower than 0.1, which indicate an 11% probability of toxicity effect. Hence, the sampling sites were determined to be the low-priority sites. PMID:24163633

  4. LABORATORY INVESTIGATIONS OF POLYCYCLIC AROMATIC HYDROCARBON FORMATION AND DESTRUCTION IN THE CIRCUMSTELLAR OUTFLOWS OF CARBON STARS

    International Nuclear Information System (INIS)

    The formation and destruction mechanisms of interstellar dust analogs formed from a variety of polycyclic aromatic hydrocarbon (PAH) and hydrocarbon molecular precursors are studied in the laboratory. We used the newly developed facility COSmIC, which simulates interstellar and circumstellar environments, to investigate both PAHs and species that include the cosmically abundant atoms O, N, and S. The species generated in a discharge plasma are detected, monitored, and characterized in situ using highly sensitive techniques that provide both spectral and ion mass information. We report here the first series of measurements obtained in these experiments which focus on the characterization of the most efficient molecular precursors in the chemical pathways that eventually lead to the formation of carbonaceous grains in the stellar envelopes of carbon stars. We compare and discuss the relative efficiencies of the various molecular precursors that lead to the formation of the building blocks of carbon grains. We discuss the most probable molecular precursors in terms of size and structure and the implications for the expected growth and destruction processes of interstellar carbonaceous dust

  5. Energetics and kinetics of anaerobic aromatic and fatty acid degradation

    Energy Technology Data Exchange (ETDEWEB)

    McInerney, M.J.

    1992-11-16

    The kinetics of benzoate degradation by the anaerobic syntrophic bacterium, Syntrophus buswellii, was studied in coculture with Desulfovibrio strain G11. The threshold value for benzoate degradation was dependent on the acetate concentration with benzoate threshold values ranging from 2.4 [mu]M at 20 mM acetate to 30.0 [mu]M at 65 mM acetate. Increasing acetate concentrations also inhibited the rate of benzoate degradation with a apparent K[sub i] for acetate inhibition of 7.0 mM. Lower threshold values were obtained when nitrate rather than sulfate was the terminal electron acceptor. These data are consistent with a thermodynamic explanation for the threshold, and suggest that there is a minimum Gibbs free energy value required for the degradation of benzoate. An acetoacetyl-CoA thiolase has been isolated from Syntrophomonas wolfei; it is apparently a key enzyme controlling the synthesis of poly-B-hydroxyalkanoate from acetyl-CoA in this organism. Kinetic characterization of the acetoacetyl-CoA thiolase from S. wolfei showed that it is similar in its structural, kinetic, and apparent regulatory properties to other biosynthetic acetoacetyl-CoA thiolases from phylogenetically distinct bacteria that synthesize PHA. Intracellular concentrations of CoA and acetyl-CoA are believed to be critical factors regulating the activity of the acetoacetyl-CoA thiolase in S. wolfei. We have also isolated and characterized several new halophilic anaerobic fermentative anaerobes. Phylogenetic analysis indicates that one of these bacteria is a new species in the genus, Haloanaerobium. Two other species appear to be members of the genus, Halobacteroides. Several halophilic acetoclastic methanogenic bacteria have also been isolated and their physiological properties are currently under investigation. We have also isolated an acetate-using dissimilatory iron-reducing bacterium.

  6. Distribution of endophytic bacteria in Alopecurus aequalis Sobol and Oxalis corniculata L. from soils contaminated by polycyclic aromatic hydrocarbons.

    Directory of Open Access Journals (Sweden)

    Anping Peng

    Full Text Available The distributions of endophytic bacteria in Alopecurus aequalis Sobol and Oxalis corniculata L. grown in soils contaminated with different levels of polycyclic aromatic hydrocarbons (PAHs were investigated with polymerase chain reaction followed by denaturing gradient gel electrophoresis technology (PCR-DGGE and cultivation methods. Twelve types of PAHs, at concentrations varying from 0.16 to 180 mg·kg(-1, were observed in the roots and shoots of the two plants. The total PAH concentrations in Alopecurus aequalis Sobol obtained from three different PAH-contaminated stations were 184, 197, and 304 mg·kg(-1, and the total PAH concentrations in Oxalis corniculata L. were 251, 346, and 600 mg·kg(-1, respectively. The PCR-DGGE results showed that the endophytic bacterial communities in the roots and shoots of the two plants were quite different, although most bacteria belonged to Firmicutes, Proteobacteria, Actinobacteria and Bacteroidetes. A total of 68 endophytic bacterial strains were isolated from different tissues of the two plants and classified into three phyla: Firmicutes, Proteobacteria and Bacteroidetes. In both plants, Bacillus spp. and Pseudomonas spp. were the dominant cultivable populations. With an increase in the PAH pollution level, the diversity and distribution of endophytic bacteria in the two plants changed correspondingly, and the number of cultivable endophytic bacterial strains decreased rapidly. Testing of the isolated endophytic bacteria for tolerance to each type of PAH showed that most isolates could grow well on Luria-Bertani media in the presence of different PAHs, and some isolates were able to grow rapidly on a mineral salt medium with a single PAH as the sole carbon and energy source, indicating that these strains may have the potential to degrade PAHs in plants. This research provides the first insight into the characteristics of endophytic bacterial populations under different PAH pollution levels and provides a

  7. Response of the bacterial community associated with a cosmopolitan marine diatom to crude oil shows a preference for the biodegradation of aromatic hydrocarbons.

    Science.gov (United States)

    Mishamandani, Sara; Gutierrez, Tony; Berry, David; Aitken, Michael D

    2016-06-01

    Emerging evidence shows that hydrocarbonoclastic bacteria (HCB) may be commonly found associated with phytoplankton in the ocean, but the ecology of these bacteria and how they respond to crude oil remains poorly understood. Here, we used a natural diatom-bacterial assemblage to investigate the diversity and response of HCB associated with a cosmopolitan marine diatom, Skeletonema costatum, to crude oil. Pyrosequencing analysis and qPCR revealed a dramatic transition in the diatom-associated bacterial community, defined initially by a short-lived bloom of Methylophaga (putative oil degraders) that was subsequently succeeded by distinct groups of HCB (Marinobacter, Polycyclovorans, Arenibacter, Parvibaculum, Roseobacter clade), including putative novel phyla, as well as other groups with previously unqualified oil-degrading potential. Interestingly, these oil-enriched organisms contributed to the apparent and exclusive biodegradation of substituted and non-substituted polycyclic aromatic hydrocarbons (PAHs), thereby suggesting that the HCB community associated with the diatom is tuned to specializing in the degradation of PAHs. Furthermore, the formation of marine oil snow (MOS) in oil-amended incubations was consistent with its formation during the Deepwater Horizon oil spill. This work highlights the phycosphere of phytoplankton as an underexplored biotope in the ocean where HCB may contribute importantly to the biodegradation of hydrocarbon contaminants in marine surface waters. PMID:26184578

  8. Microbial Degradation of Petroleum Hydrocarbon Contaminants: An Overview

    OpenAIRE

    Nilanjana Das; Preethy Chandran

    2010-01-01

    One of the major environmental problems today is hydrocarbon contamination resulting from the activities related to the petrochemical industry. Accidental releases of petroleum products are of particular concern in the environment. Hydrocarbon components have been known to belong to the family of carcinogens and neurotoxic organic pollutants. Currently accepted disposal methods of incineration or burial insecure landfills can become prohibitively expensive when amounts of contaminants are lar...

  9. Effects of methyl group on aromatic hydrocarbons on the nanostructures and oxidative reactivity of combustion-generated soot

    KAUST Repository

    Guerrero Peña, Gerardo D.J.

    2016-07-23

    The substituted and unsubstituted aromatic hydrocarbons, present in transportation fuels such as gasoline and diesel, are thought to be responsible for most of the soot particles produced during their combustion. However, the effects of the substituted alkyl groups on the aromatic hydrocarbons on their sooting tendencies, and on the physical and chemical properties of soot produced from them are not well understood. In this work, the effect of the presence of methyl groups on aromatic hydrocarbons on their sooting propensity, and on the oxidative reactivity, morphology, and chemical composition of soot generated from them in diffusion flames is studied using benzene, toluene, and m-xylene as fuels. Several experimental techniques including high resolution transmission electron microscopy and X-ray diffraction are used to identify the morphological changes in soot, whereas the elemental and thermo-gravimetric analyses, electron energy loss spectroscopy, and Fourier transform infrared spectroscopy are used to study the changes in its chemical properties and reactivity. The activation energies for soot oxidation are calculated at different conversion levels, and a trend in the reactivity of soots from benzene, toluene and m-xylene is reported. It is observed that the sizes of primary particles and graphene-like sheets, and the concentrations of aliphatics and oxygenated groups in soot particles decreased with the addition of methyl group(s) on the aromatic ring. The physicochemical changes in soot are found to support the oxidative reactivity trends. © 2016 The Combustion Institute

  10. Dispersants as used in response to the MC252-spill lead to higher mobility of polycyclic aromatic hydrocarbons in oil-contaminated Gulf of Mexico sand.

    Science.gov (United States)

    Zuijdgeest, Alissa; Huettel, Markus

    2012-01-01

    After the explosion of the Deepwater Horizon oil rig, large volumes of crude oil were washed onto and embedded in the sandy beaches and sublittoral sands of the Northern Gulf of Mexico. Some of this oil was mechanically or chemically dispersed before reaching the shore. With a set of laboratory-column experiments we show that the addition of chemical dispersants (Corexit 9500A) increases the mobility of polycyclic aromatic hydrocarbons (PAHs) in saturated permeable sediments by up to two orders of magnitude. Distribution and concentrations of PAHs, measured in the solid phase and effluent water of the columns using GC/MS, revealed that the mobility of the PAHs depended on their hydrophobicity and was species specific also in the presence of dispersant. Deepest penetration was observed for acenaphthylene and phenanthrene. Flushing of the columns with seawater after percolation of the oiled water resulted in enhanced movement by remobilization of retained PAHs. An in-situ benthic chamber experiment demonstrated that aromatic hydrocarbons are transported into permeable sublittoral sediment, emphasizing the relevance of our laboratory column experiments in natural settings. We conclude that the addition of dispersants permits crude oil components to penetrate faster and deeper into permeable saturated sands, where anaerobic conditions may slow degradation of these compounds, thus extending the persistence of potentially harmful PAHs in the marine environment. Application of dispersants in nearshore oil spills should take into account enhanced penetration depths into saturated sands as this may entail potential threats to the groundwater.

  11. Dispersants as used in response to the MC252-spill lead to higher mobility of polycyclic aromatic hydrocarbons in oil-contaminated Gulf of Mexico sand.

    Directory of Open Access Journals (Sweden)

    Alissa Zuijdgeest

    Full Text Available After the explosion of the Deepwater Horizon oil rig, large volumes of crude oil were washed onto and embedded in the sandy beaches and sublittoral sands of the Northern Gulf of Mexico. Some of this oil was mechanically or chemically dispersed before reaching the shore. With a set of laboratory-column experiments we show that the addition of chemical dispersants (Corexit 9500A increases the mobility of polycyclic aromatic hydrocarbons (PAHs in saturated permeable sediments by up to two orders of magnitude. Distribution and concentrations of PAHs, measured in the solid phase and effluent water of the columns using GC/MS, revealed that the mobility of the PAHs depended on their hydrophobicity and was species specific also in the presence of dispersant. Deepest penetration was observed for acenaphthylene and phenanthrene. Flushing of the columns with seawater after percolation of the oiled water resulted in enhanced movement by remobilization of retained PAHs. An in-situ benthic chamber experiment demonstrated that aromatic hydrocarbons are transported into permeable sublittoral sediment, emphasizing the relevance of our laboratory column experiments in natural settings. We conclude that the addition of dispersants permits crude oil components to penetrate faster and deeper into permeable saturated sands, where anaerobic conditions may slow degradation of these compounds, thus extending the persistence of potentially harmful PAHs in the marine environment. Application of dispersants in nearshore oil spills should take into account enhanced penetration depths into saturated sands as this may entail potential threats to the groundwater.

  12. Application of ultrasound and air stripping for the removal of aromatic hydrocarbons from spent sulfidic caustic for use in autotrophic denitrification as an electron donor.

    Science.gov (United States)

    Lee, Jae-Ho; Park, Jeung-Jin; Choi, Gi-Choong; Byun, Im-Gyu; Park, Tae-Joo; Lee, Tae-Ho

    2013-01-01

    Spent sulfidic caustic (SSC) produced from petroleum industry can be reused to denitrify nitrate-nitrogen via a biological nitrogen removal process as an electron donor for sulfur-based autotrophic denitrification, because it has a large amount of dissolved sulfur. However, SSC has to be refined because it also contains some aromatic hydrocarbons, typically benzene, toluene, ethylbenzene, xylene (BTEX) and phenol that are recalcitrant organic compounds. In this study, laboratory-scale ultrasound irradiation and air stripping treatment were applied in order to remove these aromatic hydrocarbons. In the ultrasound system, both BTEX and phenol were exponentially removed by ultrasound irradiation during 60 min of reaction time to give the greatest removal efficiency of about 80%. Whereas, about 95% removal efficiency of BTEX was achieved, but not any significant phenol removal, within 30 min in the air stripping system, indicating that air stripping was a more efficient method than ultrasound irradiation. However, since air stripping did not remove any significant phenol, an additional process for degrading phenol was required. Accordingly, we applied a combined ultrasound and air stripping process. In these experiments, the removal efficiencies of BTEX and phenol were improved compared to the application of ultrasound and air stripping alone. Thus, the combined ultrasound and air stripping treatment is appropriate for refining SSC.

  13. Microbial diversity and hydrocarbon degrading gene capacity of a crude oil field soil as determined by metagenomics analysis.

    Science.gov (United States)

    Abbasian, Firouz; Palanisami, Thavamani; Megharaj, Mallavarapu; Naidu, Ravi; Lockington, Robin; Ramadass, Kavitha

    2016-05-01

    Soils contaminated with crude oil are rich sources of enzymes suitable for both degradation of hydrocarbons through bioremediation processes and improvement of crude oil during its refining steps. Due to the long term selection, crude oil fields are unique environments for the identification of microorganisms with the ability to produce these enzymes. In this metagenomic study, based on Hiseq Illumina sequencing of samples obtained from a crude oil field and analysis of data on MG-RAST, Actinomycetales (9.8%) were found to be the dominant microorganisms, followed by Rhizobiales (3.3%). Furthermore, several functional genes were found in this study, mostly belong to Actinobacteria (12.35%), which have a role in the metabolism of aliphatic and aromatic hydrocarbons (2.51%), desulfurization (0.03%), element shortage (5.6%), and resistance to heavy metals (1.1%). This information will be useful for assisting in the application of microorganisms in the removal of hydrocarbon contamination and/or for improving the quality of crude oil. © 2016 American Institute of Chemical Engineers Biotechnol. Prog., 32:638-648, 2016. PMID:26914145

  14. Microbial diversity and hydrocarbon degrading gene capacity of a crude oil field soil as determined by metagenomics analysis.

    Science.gov (United States)

    Abbasian, Firouz; Palanisami, Thavamani; Megharaj, Mallavarapu; Naidu, Ravi; Lockington, Robin; Ramadass, Kavitha

    2016-05-01

    Soils contaminated with crude oil are rich sources of enzymes suitable for both degradation of hydrocarbons through bioremediation processes and improvement of crude oil during its refining steps. Due to the long term selection, crude oil fields are unique environments for the identification of microorganisms with the ability to produce these enzymes. In this metagenomic study, based on Hiseq Illumina sequencing of samples obtained from a crude oil field and analysis of data on MG-RAST, Actinomycetales (9.8%) were found to be the dominant microorganisms, followed by Rhizobiales (3.3%). Furthermore, several functional genes were found in this study, mostly belong to Actinobacteria (12.35%), which have a role in the metabolism of aliphatic and aromatic hydrocarbons (2.51%), desulfurization (0.03%), element shortage (5.6%), and resistance to heavy metals (1.1%). This information will be useful for assisting in the application of microorganisms in the removal of hydrocarbon contamination and/or for improving the quality of crude oil. © 2016 American Institute of Chemical Engineers Biotechnol. Prog., 32:638-648, 2016.

  15. Field effect transistors based on polycyclic aromatic hydrocarbons for the detection and classification of volatile organic compounds.

    Science.gov (United States)

    Bayn, Alona; Feng, Xinliang; Müllen, Klaus; Haick, Hossam

    2013-04-24

    We show that polycyclic aromatic hydrocarbon (PAH) based field effect transistor (FET) arrays can serve as excellent chemical sensors for the detection of volatile organic compounds (VOCs) under confounding humidity conditions. Using these sensors, w/o complementary pattern recognition methods, we study the ability of PAH-FET(s) to: (i) discriminate between aromatic and non-aromatic VOCs; (ii) distinguish polar and non-polar non-aromatic compounds; and to (iii) identify specific VOCs within the subgroups (i.e., aromatic compounds, polar non-aromatic compounds, non-polar non-aromatic compounds). We further study the effect of water vapor on the sensor array's discriminative ability and derive patterns that are stable when exposed to different constant values of background humidity. Patterns based on different independent electronic features from an array of PAH-FETs may bring us one step closer to creating a unique fingerprint for individual VOCs in real-world applications in atmospheres with varying levels of humidity.

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

    Science.gov (United States)

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

    2013-12-01

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

  17. Vertical distribution and anaerobic biodegradation of polycyclic aromatic hydrocarbons in mangrove sediments in Hong Kong, South China

    Energy Technology Data Exchange (ETDEWEB)

    Li, Chun-Hua [Department of Biology and Chemistry, City University of Hong Kong, Tat Chee Avenue, Kowloon (Hong Kong); Zhou, Hong-Wei [Department of Environmental Health Science, School of Public Health and Tropical Medicine, Southern Medical University, Guangzhou (China); Wong, Yuk-Shan [Department of Biology, The Hong Kong University of Science and Technology (Hong Kong); Tam, Nora Fung-Yee, E-mail: bhntam@cityu.edu.hk [Department of Biology and Chemistry, City University of Hong Kong, Tat Chee Avenue, Kowloon (Hong Kong)

    2009-10-15

    The vertical distribution of polycyclic aromatic hydrocarbons (PAHs) at different sediment depths, namely 0-2 cm, 2-4 cm, 4-6 cm, 6-10 cm, 10-15 cm and 15-20 cm, in one of the most contaminated mangrove swamps, Ma Wan, Hong Kong was investigated. It was the first time to study the intrinsic potential of deep sediment to biodegrade PAHs under anaerobic conditions and the abundance of electron acceptors in sediment for anaerobic degradation. Results showed that the total PAHs concentrations (summation of 16 US EPA priority PAHs) increased with sediment depth. The lowest concentration (about 1300 ng g{sup -1} freeze-dried sediment) and the highest value (around 5000 ng g{sup -1} freeze-dried sediment) were found in the surface layer (0-2 cm) and deeper layer (10-15 cm), respectively. The percentage of high molecular weight (HMW) PAHs (4 to 6 rings) to total PAHs was more than 89% at all sediment depths. The ratio of phenanthrene to anthracene was less than 10 while fluoranthene to pyrene was around 1. Negative redox potentials (Eh) were recorded in all of the sediment samples, ranging from - 170 to - 200 mv, with a sharp decrease at a depth of 6 cm then declined slowly to 20 cm. The results suggested that HMW PAHs originated from diesel-powered fishing vessels and were mainly accumulated in deep anaerobic sediments. Among the electron acceptors commonly used by anaerobic bacteria, sulfate was the most dominant, followed by iron(III), nitrate and manganese(IV) was the least. Their concentrations also decreased with sediment depth. The population size of total anaerobic heterotrophic bacteria increased with sediment depth, reaching the peak number in the middle layer (4-6 cm). In contrast, the aerobic heterotrophic bacterial count decreased with sediment depth. It was the first time to apply a modified electron transport system (ETS) method to evaluate the bacterial activities in the fresh sediment under PAH stress. The vertical drop of the ETS activity suggested that

  18. Effect of the Structure of Cations and Anions of Ionic Liquids on Separation of Aromatics from Hydrocarbon Mixtures

    Institute of Scientific and Technical Information of China (English)

    Liu Yansheng; Zhang Zhongxin; Zhang Guofu; Liu Zhichang; Hu Yufeng; Shi Quan; Ji Dejun

    2006-01-01

    The effects of the structure of typical cations and anions of ionic liquids on the separation of benzene and toluene from aromatic/paraffin mixtures were studied. The results showed that the corresponding separation factors were considerably larger than those of the traditional solvents (Benzene+Hexane+sulfolane), and that the ionic liquids could be used as novel solvents for the separation of aromatics from hydrocarbon mixtures. The key parameters governing the ability of ionic liquids for separating aromatics from hydrocarbon sources were investigated. It was found that the effectiveness of the ionic liquids, based on the same anion, changed in the cation order of [BIqu]+< [BPy]+< [BMIM]+. The selectivity of the ionic liquid toward aromatics decreased apparently with the increasing length of the substituted alkyl chain of its cationic head ring. The separation factors, based on the same cation, changed in the anion order of [Tf2N]-<[PF6]-<[BF4]-<[C2H5SO4]-. The solubilities of the aromatics were greater in the ionic liquids based on the former three anions than that in the ionic liquids involving [C2H5SO4]-.

  19. Exploration of hydrocarbon degrading bacteria on soils contaminated by crude oil from South Sumatera

    Directory of Open Access Journals (Sweden)

    A. Napoleon

    2014-07-01

    Full Text Available The goal of this research was to explore hydrocarbon degrading bacteria on crude oil contaminated soil with potential to degrade hydrocarbon in oil pollutant. The research started by early August 2013 till January 2014. Soil sampling for this research was taken on several places with contaminated soil location such as Benakat, Rimau, and Pengabuan all of it located in South Sumatera. Conclusion from this research Isolates obtained from three (3 sites of contaminated soil and treated using SBS medium were Bacillus cereus, Pseudomonas aeruginosa, Klebsiella pnumoniae, Streptococcus beta hemolisa, Proteus mirabilis, Staphylococcus epidermis and Acinotobacter calcoaceticus. Isolates that survived on 300 ppm of hydrocarbon concentration were Bacillus cereus, Pseudomonas aeruginosa and Acinetobacter cakciaceticus Selected isolates posses the ability to degrade hydrocarbon by breaking hydrocarbon substance as the energy source to support isolates existence up to 1,67 TPH level. Based on results accomplish by this research, we urge for further research involving the capacity of isolates to degrade wide variety of hydrocarbon substance and more to develop the potential of these bacteria for bioremediation.

  20. Source Identification of Polycyclic Aromatic Hydrocarbons by Diagnostic Ratios and Positive Matrix Factorization

    Science.gov (United States)

    Dvorska, A.; Jarkovsky, J.; Lammel, G.; Klanova, J.

    2009-04-01

    Although polycyclic aromatic hydrocarbons (PAHs) are also of natural origin, in many regions their environmental concentrations have strongly increased due to human activities. These semivolatile organic compounds are generally formed during incomplete combustion. Other sources include volatilization from unburned petroleum or tire abrasion in road traffic. Among all pollutants PAHs pose the highest human health hazard in Europe (WHO, 2003). A multivariate statistical method, positive matrix factorization (PMF; Paatero, 1997), and diagnostic ratios of individual PAHs (e.g. Yunker et al., 2002) are used for PAH source identification in central Europe. To minimise confounding factors such as differences in volatility, water solubility, adsorption etc., diagnostic ratios should be restricted to PAHs of similar molecular mass (Readman et al., 1987). Furthermore, different reactivities are limiting. Nevertheless, the application of PAH diagnostic ratios is often inconclusive, because substance patterns (profiles) have not been reported for all sources and ranges for various sources overlap. The complete profiles are made use of by statistical methods such as factor analysis, UNMIX and PMF (Tauler et al., 2006). However, these methods can be unreliable, because of incomplete knowledge of source profiles and the analysis' sensitivity to the data distribution. A unique 12-year data set of concentrations of PAHs (16 individual substances, 2 phases, weekly) in air, measured at the regional observatory Košetice, Czech Republic, is examined, together with shorter time series from Leipzig (urban background) and Schwartenberg (subalpine mountain background), Germany. Also, retene and coronene as specific source markers measured in Košetice from 2006 on are included into the analysis. An extensive literature search on PAH emission profiles was conducted. This data set was accomplished by measurements at sites in the Zlínsko region, Czech Republic, which are strongly dominated