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Sample records for chrysene

  1. Infrared Spectroscopic Analysis of Chrysene and 1.2-Benzanthracence in Wax films

    Institute of Scientific and Technical Information of China (English)

    Md. Naziruddin Khan; A. S. Al-Dwayyan; Z. H. Zaidi

    2006-01-01

    @@ Chrysene and 1.2-benzanthracene are successfully doped in a solid wax film and their vibrational spectra in2000-400 cm- 1 are discussed. The harmonic frequencies and relative intensities of both the molecules observed in the film are compared with theoretical values calculated by the density functional theory (DFT) model as well as with the previous experimental data.

  2. Bioremediation of phenanthrene, chrysene and benzo[a]pyrene by fungi screened from nature

    Directory of Open Access Journals (Sweden)

    Tony Hadibarata

    2009-09-01

    Full Text Available Laccase of Polyporus sp. S133 was able to oxidize most of the 3 different rings amount polycyclic aromatic hydrocarbons (PAHs tested. Phenanthrene was removed by 89% followed by chrysene and benzo[a]pyrene which were oxidized by 66 and 55%, respectively. Addition of 1-hydroxybenzotriazole (HBT to the reaction mixture increased oxidation of PAHs, especially phenanthrene was almost completely removed from the reaction mixture. Oxidation of chrysene and benzo[a]anthracene increased 12 and 10% with the mediator to 78 and 65% in the presence of HBT. PAH-quinones as oxidation products were formed from all PAH to different extents. A part of PAH was polymerized in the laccase/mediator system to products of weight-average molecular weight (MW. The correlation of the ionization potentials of PAH with the oxidation of these compounds is limited to the alternating PAH.

  3. Titanium dioxide nanoparticles provide protection against polycyclic aromatic hydrocarbon BaP and chrysene-induced perturbation of DNA repair machinery: A computational biology approach.

    Science.gov (United States)

    Dhasmana, Anupam; Jamal, Qazi Mohd Sajid; Gupta, Richa; Siddiqui, Mohd Haris; Kesari, Kavindra Kumar; Wadhwa, Gulshan; Khan, Saif; Haque, Shafiul; Lohani, Mohtashim

    2016-07-01

    We examined the interaction of polycyclic hydrocarbons (PAHs) like benzo-α-pyrene (BaP), chrysene, and their metabolites 7,8-dihydro-7,8-dihydroxybenzo(a)pyrene,9,10-oxide (BPDE) and chrysene 1,2-diol-3,4-epoxide-2 (CDE), with the enzymes involved in DNA repair. We investigated interaction of 120 enzymes with PAHs and screened out 40 probable targets among DNA repair enzymes, on the basis of higher binding energy than positive control. Out of which, 20 enzymes lose their function in the presence of BaP, chrysene, and their metabolites, which may fetter DNA repair pathways resulting in damage accumulation and finally leading to cancer formation. We propose the use of nanoparticles as a guardian against the PAH's induced toxicity. PAHs enter the cell via aryl hydrocarbon receptor (AHR). TiO2 NP showed a much higher docking score with AHR (12,074) as compared with BaP and chrysene with AHR (4,600 and 4,186, respectively), indicating a preferential binding of TiO2 NP with the AHR. Further, docking of BaP and chrysene with the TiO2 NP bound AHR complex revealed their strong adsorption on TiO2 NP itself, and not on their original binding site (at AHR). TiO2 NPs thereby prevent the entry of PAHs into the cell via AHR and hence protect cells against the deleterious effects induced by PAHs.

  4. Tissue Distribution, Excretion and Pharmacokinetics of the Environmental Pollutant Dibenzo[def,p]chrysene in Mice.

    Science.gov (United States)

    Sun, Yuan-Wan; El-Bayoumy, Karam; Aliaga, Cesar; Awad, Alaa S; Gowda, Krishne; Amin, Shantu; Chen, Kun-Ming

    2015-07-20

    Dibenzo[def,p]chrysene (DBP), a representative example of the class of polycyclic aromatic hydrocarbon (PAH), is known to induce tumors in multiple organ sites including the ovary, lung, mammary glands, and oral cavity in rodents. The goal of this study was to test the hypothesis that the levels of DBP and its metabolites that reach and retain the levels for an extended time in the target organs as well as the capacity of these organs to metabolize this carcinogen to active metabolites that can damage DNA may account for its tissue selective tumorigenicity. Therefore, we used the radiolabeled [(3)H] DBP to accurately assess the tissue distribution, excretion, and pharmacokinetics of this carcinogen. We also compared the levels of DBPDE-DNA adducts in a select target organ (ovary) and nontarget organs (kidney and liver) in mice treated orally with DBP. Our results showed that after 1 week, 91.40 ± 7.23% of the radioactivity was recovered in the feces; the corresponding value excreted in the urine was less than 2% after 1 week. After 24 h, the stomach had the highest radioactivity followed by the intestine and the liver; however, after 1 week, levels of the radioactivity in these organs were the lowest among tissues examined including the ovary and liver; the pharmacokinetic analysis of DBP was conducted using a one compartment open model. The level of (-)-anti-trans-DBPDE-dA in the ovaries (8.91 ± 0.08 adducts/10(7) dA) was significantly higher (p < 0.01) than the levels of adducts in kidneys (0.69 ± 0.09 adducts/10(7) dA) and livers (0.63 ± 0.11 adducts/10(7) dA). Collectively, the results of the tissue distribution and pharmacokinetic analysis may not fully support our hypothesis, but the capacity of the target organs vs nontarget organs to metabolize DBP to active intermediates that can damage DNA may account for its tissue selective tumorigenicity. PMID:26034881

  5. Impact of dissolved humic acid on the bioavailability of acenaphthene and chrysene assessed by membrane-based passive samplers

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Dissolved organic carbon (DOC) is known to reduce the bioavailability of hydrophobic organic compounds (HOCs) in aqueous environments. This reduction occurs as a result of adsorption to DOC, apparently reducing the freely dissolved concentration of HOCs. In the present study, triolein-embedded cellulose acetate membrane (TECAM) and Japanese medaka (Oryzias latipes) were used to measure the uptake of acenaphthene and chrysene in the presence of commercial humic acid (HA) at different concentrations (0―15 mg C·L-1) under controlled laboratory conditions. Apparent uptake rate constants for PAHs in TECAM and medaka were compared and DOC-water partition coefficients (KDOCs) of two PAHs were calculated with different sampling methods by model fit. Results showed that HA present in water significantly reduced the uptake of PAHs in TECAM and medaka. The obtained values of log KDOC of acenaphthene and chrysene measured by TECAM were 4.63 and 5.83, respectively, whereas biologically determined values were 4.52 and 5.76, respectively. These log KDOC values were comparable to earlier published KDOCs toward commercial HA, thereby indicating that TECAM accumulated only the freely dissolved fraction of chemicals and uptake PAHs in a manner similar to that of fish. All these results suggested that the TECAM method can provide a good means for assessing the impact of DOC on bioavailability of PAHs in the aqueous environment.

  6. Quantitative structure–activity relationships for chronic toxicity of alkyl-chrysenes and alkyl-benz[a]anthracenes to Japanese medaka embryos (Oryzias latipes)

    International Nuclear Information System (INIS)

    Highlights: • Medaka embryos were exposed to alkyl chrysenes and benzo[a]anthracenes (BAA). • Concentrations were kept constant by partition controlled delivery. • Chrysene was not toxic within solubility limits, in contrast to BAA. • Alkylation increased the toxicity of chrysene and BAA. • Toxicity was related to hydrophobicity and to specific modes of action. - Abstract: Alkylated polycyclic aromatic hydrocarbons (alkyl-PAHs) are a class of compounds found at significant concentrations in crude oils, and likely the main constituents responsible for the chronic toxicity of oil to fish. Alkyl substituents at different locations on the aromatic rings change the size and shape of PAH molecules, which results in different interactions with tissue receptors and different severities of toxicity. The present study is the first to report the toxicity of several alkylated derivatives of chrysene and benz[a]anthracene to the embryos of Japanese medaka (Oryzias latipes) using the partition controlled delivery (PCD) method of exposure. The PCD method maintained the desired exposure concentrations by equilibrium partitioning of hydrophobic test compounds from polydimethylsiloxane (PDMS) films. Test concentrations declined by only 13% over a period of 17 days. Based on the prevalence of signs of blue sac disease (BSD), as expressed by median effective concentrations (EC50s), benz[a]anthracene (B[a]A) was more toxic than chrysene. Alkylation generally increased toxicity, except at position 2 of B[a]A. Alkyl-PAHs substituted in the middle region had a lower EC50 than those substituted at the distal region. Except for B[a]A and 7-methylbenz[a]anthracene (7-MB), estimated EC50 values were higher than their solubility limits, which resulted in limited toxicity within the range of test concentrations. The regression between log EC50s and log Kow values provided a rough estimation of structure–activity relationships for alkyl-PAHs, but Kow alone did not provide a complete

  7. Embryotoxic effects of benzo[a]pyrene, chrysene and 7,12-dimethylbenz[a]-anthracene in petroleum hydrocarbon mixtures in mallard ducks

    Science.gov (United States)

    Hoffman, D.J.; Gay, M.L.

    1981-01-01

    Studies with different avian species have revealed that surface applications of microliter amounts of some crude and fuel oils that coat less than 70% of the egg surface result in considerable reduction in hatching with teratogenicity and stunted growth. Other stUdies have shown that the embryo toxicity is dependent on the aromatic hydrocarbon content, further suggesting that the toxicity is due to causes other than asphyxia. In the present study the effects of three polycyclic aromatic hydrocarbons identified in petroleum were examined on mallard (Anas platyrhynchos) embryo development. Addition of benzo[a]pyrene (BaP), chrysene, or 7,7 2-dimethylbenz[ a]anthracene (DMBA) to a synthetic petroleum hydrocarbon mixture of known composition and relatively low embryotoxicity resulted in embryo toxicity that was enhanced or equal to that of crude oil when 10 :I was applied externally to eggs at 72 h of development. The order of ability to enhance embryo toxicity was DMBA > BaP > chrysene. The temporal pattern of embryonic death was similar to that reported after exposure to crude oil, with additional mortality occurring after outgrowth of the chorioallantois. Retarded growth, as reflected by embryonic body weight, crown-rump length, and bill length, was accompanied by teratogenicity. Abnormal embryos exhibited extreme stunting; eye, brain, and bill defects; and incomplete ossification. Gas chromatographic-mass spectral analysis of externally treated eggs showed the passage of aromatic hydrocarbons including chrysene through the shell and shell membranes to the developing embryos. These findings suggest that the presence of polycyclic aromatic hydrocarbons in petroleum, including BaP, chrysene, and DMBA, significantly enhances the overall embryotoxicity in avian species.

  8. Arsenite Interacts with Dibenzo[def,p]chrysene (DBC) at Low Levels to Suppress Bone Marrow Lymphoid Progenitors in Mice.

    Science.gov (United States)

    Ezeh, Peace C; Lauer, Fredine T; Liu, Ke Jian; Hudson, Laurie G; Burchiel, Scott W

    2015-07-01

    Arsenite (As(+3)) and dibenzo[def,p]chrysene (DBC), a polycyclic aromatic hyrdrocarbon (PAH), are found in nature as environmental contaminants. Both are known to individually suppress the immune system of humans and mice. In order to determine their potential interactive and combined immunosuppressive effects, we examined murine bone marrow (BM) immune progenitor cells' responses following combined oral exposures at very low levels of exposure to As(+3) and DBC. Oral 5-day exposure to DBC at 1 mg/kg (cumulative dose) was found to suppress mouse BM lymphoid progenitor cells, but not the myeloid progenitors. Previously established no-effect doses of As(+3) in drinking water (19 and 75 ppb for 30 days) produced more lymphoid suppression in the bone marrow when mice were concomitantly fed a low dose of DBC during the last 5 days. The lower dose (19 ppb) As(+3) had a stronger suppressive effect with DBC than the higher dose (75 ppb). Thus, the interactive toxicity of As(+3) and DBC in vivo could be As(+3) dose dependent. In vitro, the suppressive interaction of As(+3) and DBC was also evident at low concentrations (0.5 nM), but not at higher concentrations (5 nM) of As(+3). These studies show potentially important interactions between As(+3) and DBC on mouse BM at extremely low levels of exposure in vivo and in vitro. PMID:25739538

  9. Quantitative structure–activity relationships for chronic toxicity of alkyl-chrysenes and alkyl-benz[a]anthracenes to Japanese medaka embryos (Oryzias latipes)

    Energy Technology Data Exchange (ETDEWEB)

    Lin, Hongkang [Department of Biology, Queen' s University, Kingston, Ontario K7L3N6 (Canada); Morandi, Garrett D. [School of Environmental Studies, Queen' s University, Kingston, Ontario K7L3N6 (Canada); Brown, R. Stephen [School of Environmental Studies, Queen' s University, Kingston, Ontario K7L3N6 (Canada); Department of Chemistry, Queen' s University, Kingston, Ontario K7L3N6 (Canada); Snieckus, Victor; Rantanen, Toni [Department of Chemistry, Queen' s University, Kingston, Ontario K7L3N6 (Canada); Jørgensen, Kåre B. [Department of Mathematics and Natural Sciences, University of Stavanger, 4036 Stavanger (Norway); Hodson, Peter V., E-mail: peter.hodson@queensu.ca [Department of Biology, Queen' s University, Kingston, Ontario K7L3N6 (Canada); School of Environmental Studies, Queen' s University, Kingston, Ontario K7L3N6 (Canada)

    2015-02-15

    Highlights: • Medaka embryos were exposed to alkyl chrysenes and benzo[a]anthracenes (BAA). • Concentrations were kept constant by partition controlled delivery. • Chrysene was not toxic within solubility limits, in contrast to BAA. • Alkylation increased the toxicity of chrysene and BAA. • Toxicity was related to hydrophobicity and to specific modes of action. - Abstract: Alkylated polycyclic aromatic hydrocarbons (alkyl-PAHs) are a class of compounds found at significant concentrations in crude oils, and likely the main constituents responsible for the chronic toxicity of oil to fish. Alkyl substituents at different locations on the aromatic rings change the size and shape of PAH molecules, which results in different interactions with tissue receptors and different severities of toxicity. The present study is the first to report the toxicity of several alkylated derivatives of chrysene and benz[a]anthracene to the embryos of Japanese medaka (Oryzias latipes) using the partition controlled delivery (PCD) method of exposure. The PCD method maintained the desired exposure concentrations by equilibrium partitioning of hydrophobic test compounds from polydimethylsiloxane (PDMS) films. Test concentrations declined by only 13% over a period of 17 days. Based on the prevalence of signs of blue sac disease (BSD), as expressed by median effective concentrations (EC50s), benz[a]anthracene (B[a]A) was more toxic than chrysene. Alkylation generally increased toxicity, except at position 2 of B[a]A. Alkyl-PAHs substituted in the middle region had a lower EC50 than those substituted at the distal region. Except for B[a]A and 7-methylbenz[a]anthracene (7-MB), estimated EC50 values were higher than their solubility limits, which resulted in limited toxicity within the range of test concentrations. The regression between log EC50s and log K{sub ow} values provided a rough estimation of structure–activity relationships for alkyl-PAHs, but K{sub ow} alone did not provide

  10. Differential modulation of dibenzo[def,p]chrysene transplacental carcinogenesis: Maternal diets rich in indole-3-carbinol versus sulforaphane

    Energy Technology Data Exchange (ETDEWEB)

    Shorey, Lyndsey E.; Madeen, Erin P. [Department of Environmental and Molecular Toxicology, Oregon State University, Corvallis, OR, 97331 (United States); Linus Pauling Institute, Oregon State University, Corvallis, OR, 97331 (United States); Atwell, Lauren L.; Ho, Emily [Linus Pauling Institute, Oregon State University, Corvallis, OR, 97331 (United States); School of Biological and Population Health Sciences, Oregon State University, Corvallis, OR, 97331 (United States); Löhr, Christiane V. [Linus Pauling Institute, Oregon State University, Corvallis, OR, 97331 (United States); College of Veterinary Medicine, Oregon State University, Corvallis, OR, 97331 (United States); Pereira, Clifford B. [Department of Statistics, Oregon State University, Corvallis, OR, 97331 (United States); Dashwood, Roderick H. [Department of Environmental and Molecular Toxicology, Oregon State University, Corvallis, OR, 97331 (United States); Linus Pauling Institute, Oregon State University, Corvallis, OR, 97331 (United States); Williams, David E., E-mail: david.williams@oregonstate.edu [Department of Environmental and Molecular Toxicology, Oregon State University, Corvallis, OR, 97331 (United States); Linus Pauling Institute, Oregon State University, Corvallis, OR, 97331 (United States)

    2013-07-01

    Cruciferous vegetable components have been documented to exhibit anticancer properties. Targets of action span multiple mechanisms deregulated during cancer progression, ranging from altered carcinogen metabolism to the restoration of epigenetic machinery. Furthermore, the developing fetus is highly susceptible to changes in nutritional status and to environmental toxicants. Thus, we have exploited a mouse model of transplacental carcinogenesis to assess the impact of maternal dietary supplementation on cancer risk in offspring. In this study, transplacental and lactational exposure to a maternal dose of 15 mg/Kg B.W. of dibenzo[def,p]chrysene (DBC) resulted in significant morbidity of offspring due to an aggressive T-cell lymphoblastic lymphoma. As in previous studies, indole-3-carbinol (I3C, feed to the dam at 100, 500 or 1000 ppm), derived from cruciferous vegetables, dose-dependently reduced lung tumor multiplicity and also increased offspring survival. Brussels sprout and broccoli sprout powders, selected for their relative abundance of I3C and the bioactive component sulforaphane (SFN), respectively, surprisingly enhanced DBC-induced morbidity and tumorigenesis when incorporated into the maternal diet at 10% wt/wt. Purified SFN, incorporated in the maternal diet at 400 ppm, also decreased the latency of DBC-dependent morbidity. Interestingly, I3C abrogated the effect of SFN when the two purified compounds were administered in equimolar combination (500 ppm I3C and 600 ppm SFN). SFN metabolites measured in the plasma of neonates positively correlated with exposure levels via the maternal diet but not with offspring mortality. These findings provide justification for further study of the safety and bioactivity of cruciferous vegetable phytochemicals at supplemental concentrations during the perinatal period. - Highlights: • Dietary supplementation may modulate cancer risk in a mouse model of lymphoma. • Cruciferous vegetables may not contain sufficient I3C

  11. Synthesis of a polycyclic aromatic hydrocarbon marked with carbon-14: (b, d e f) dibenzo-chrysene {sup 14}C-7,14; Synthese d'un hydrocarbure aromatique polycyclique marque au carbone 14: le dibenzo (b, d e f) chrysene {sup 14}C-7,14

    Energy Technology Data Exchange (ETDEWEB)

    Chatelain, G. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1965-07-01

    (b, d e f) dibenzo-chrysene C-7,14 has been synthesized from radioactive carbon dioxide and the organic magnesium compound derived from 1,5 dibromo naphthalene. The product has been purified by a very precise series of fractionated chromatographs on alumina having a chromatographic activity. This has necessitated the development of a special technique. (author) [French] Le dibenzo (b, d e f) chrysene 14C-7,14 a ete synthetise au depart de gaz carbonique radioactif et de bis-organomagnesien derive du dibromo-1,5 naphtalene. Le produit a ete purifie par une serie de chromatographies fractionnees sur alumine d'activite chromatographique tres precise. Ceci a fait l'objet d'une mise au point de technique. (auteur)

  12. Polycyclic aromatic hydrocarbons as skin carcinogens: Comparison of benzo[a]pyrene, dibenzo[def,p]chrysene and three environmental mixtures in the FVB/N mouse

    Energy Technology Data Exchange (ETDEWEB)

    Siddens, Lisbeth K.; Larkin, Andrew [Department of Environmental and Molecular Toxicology, Oregon State University (United States); Superfund Research Center, Oregon State University (United States); Krueger, Sharon K. [Superfund Research Center, Oregon State University (United States); The Linus Pauling Institute, Oregon State University (United States); Bradfield, Christopher A. [McArdle Laboratory for Cancer Research, University of Wisconsin, Madison, WI 53706 (United States); Waters, Katrina M.; Tilton, Susan C. [Superfund Research Center, Oregon State University (United States); Computational Biology and Bioinformatics Group, Pacific Northwest National Laboratory, Richland, WA 99352 (United States); Pereira, Cliff B. [Superfund Research Center, Oregon State University (United States); Deptartment of Statistics, Oregon State University, Corvallis, OR 97331 (United States); Environmental Health Sciences Center, Oregon State University, Corvallis, OR 97331 (United States); Löhr, Christiane V. [Environmental Health Sciences Center, Oregon State University, Corvallis, OR 97331 (United States); College of Veterinary Medicine, Oregon State University, Corvallis, OR 97331 (United States); Arlt, Volker M.; Phillips, David H. [Analytical and Environmental Sciences Division, MRC-HPA Centre for Environment and Health, King' s College London, London SE1 9NH (United Kingdom); Williams, David E., E-mail: david.williams@oregonstate.edu [Department of Environmental and Molecular Toxicology, Oregon State University (United States); Superfund Research Center, Oregon State University (United States); The Linus Pauling Institute, Oregon State University (United States); Environmental Health Sciences Center, Oregon State University, Corvallis, OR 97331 (United States); and others

    2012-11-01

    The polycyclic aromatic hydrocarbon (PAH), benzo[a]pyrene (BaP), was compared to dibenzo[def,p]chrysene (DBC) and combinations of three environmental PAH mixtures (coal tar, diesel particulate and cigarette smoke condensate) using a two stage, FVB/N mouse skin tumor model. DBC (4 nmol) was most potent, reaching 100% tumor incidence with a shorter latency to tumor formation, less than 20 weeks of 12-O-tetradecanoylphorbol-13-acetate (TPA) promotion compared to all other treatments. Multiplicity was 4 times greater than BaP (400 nmol). Both PAHs produced primarily papillomas followed by squamous cell carcinoma and carcinoma in situ. Diesel particulate extract (1 mg SRM 1650b; mix 1) did not differ from toluene controls and failed to elicit a carcinogenic response. Addition of coal tar extract (1 mg SRM 1597a; mix 2) produced a response similar to BaP. Further addition of 2 mg of cigarette smoke condensate (mix 3) did not alter the response with mix 2. PAH-DNA adducts measured in epidermis 12 h post initiation and analyzed by {sup 32}P post‐labeling, did not correlate with tumor incidence. PAH‐dependent alteration in transcriptome of skin 12 h post initiation was assessed by microarray. Principal component analysis (sum of all treatments) of the 922 significantly altered genes (p < 0.05), showed DBC and BaP to cluster distinct from PAH mixtures and each other. BaP and mixtures up-regulated phase 1 and phase 2 metabolizing enzymes while DBC did not. The carcinogenicity with DBC and two of the mixtures was much greater than would be predicted based on published Relative Potency Factors (RPFs). -- Highlights: ► Dibenzo[def,p]chrysene (DBC), 3 PAH mixtures, benzo[a]pyrene (BaP) were compared. ► DBC and 2 PAH mixtures were more potent than Relative Potency Factor estimates. ► Transcriptome profiles 12 hours post initiation were analyzed by microarray. ► Principle components analysis of alterations revealed treatment-based clustering. ► DBC gave a unique

  13. The anharmonic quartic force field infrared spectra of five non-linear polycyclic aromatic hydrocarbons: Benz[a]anthracene, chrysene, phenanthrene, pyrene, and triphenylene.

    Science.gov (United States)

    Mackie, Cameron J; Candian, Alessandra; Huang, Xinchuan; Maltseva, Elena; Petrignani, Annemieke; Oomens, Jos; Mattioda, Andrew L; Buma, Wybren Jan; Lee, Timothy J; Tielens, Alexander G G M

    2016-08-28

    The study of interstellar polycyclic aromatic hydrocarbons (PAHs) relies heavily on theoretically predicted infrared spectra. Most earlier studies use scaled harmonic frequencies for band positions and the double harmonic approximation for intensities. However, recent high-resolution gas-phase experimental spectroscopic studies have shown that the harmonic approximation is not sufficient to reproduce experimental results. In our previous work, we presented the anharmonic theoretical spectra of three linear PAHs, showing the importance of including anharmonicities into the theoretical calculations. In this paper, we continue this work by extending the study to include five non-linear PAHs (benz[a]anthracene, chrysene, phenanthrene, pyrene, and triphenylene), thereby allowing us to make a full assessment of how edge structure, symmetry, and size influence the effects of anharmonicities. The theoretical anharmonic spectra are compared to spectra obtained under matrix isolation low-temperature conditions, low-resolution, high-temperature gas-phase conditions, and high-resolution, low-temperature gas-phase conditions. Overall, excellent agreement is observed between the theoretical and experimental spectra although the experimental spectra show subtle but significant differences. PMID:27586928

  14. The anharmonic quartic force field infrared spectra of five non-linear polycyclic aromatic hydrocarbons: Benz[a]anthracene, chrysene, phenanthrene, pyrene, and triphenylene

    Science.gov (United States)

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

    2016-08-01

    The study of interstellar polycyclic aromatic hydrocarbons (PAHs) relies heavily on theoretically predicted infrared spectra. Most earlier studies use scaled harmonic frequencies for band positions and the double harmonic approximation for intensities. However, recent high-resolution gas-phase experimental spectroscopic studies have shown that the harmonic approximation is not sufficient to reproduce experimental results. In our previous work, we presented the anharmonic theoretical spectra of three linear PAHs, showing the importance of including anharmonicities into the theoretical calculations. In this paper, we continue this work by extending the study to include five non-linear PAHs (benz[a]anthracene, chrysene, phenanthrene, pyrene, and triphenylene), thereby allowing us to make a full assessment of how edge structure, symmetry, and size influence the effects of anharmonicities. The theoretical anharmonic spectra are compared to spectra obtained under matrix isolation low-temperature conditions, low-resolution, high-temperature gas-phase conditions, and high-resolution, low-temperature gas-phase conditions. Overall, excellent agreement is observed between the theoretical and experimental spectra although the experimental spectra show subtle but significant differences.

  15. Synthesis, microsome-mediated metabolism, and identification of major metabolites of environmental pollutant naphtho(8,1,2-ghi)chrysene

    Energy Technology Data Exchange (ETDEWEB)

    Sharma, A.K.; Gowdahalli, K.; Gimbor, M.; Amin, S. [Penn State College of Medicine, Hershey, PA (United States)

    2008-05-15

    Naphtho(8,1,2-ghi)chrysene, commonly known as naphtho(1,2-e)pyrene (N(1,2-e)P) is a widespread environmental pollutant, identified in coal tar extract, air borne particulate matter, marine sediment, cigarette smoke condensate, and vehicle exhaust. Herein, we determined the ability of rat liver microsomes to metabolize N(1,2-e)P and an unequivocal assignment of the metabolites by comparing them with independently,synthesized standards. We developed the synthesis of both the fjord region and the K-region dihydrodiols and various phenolic derivatives for metabolite identification. In summary, N(1,2-e)P trans-11, 12-dihydrodiol was the major metabolite formed along with N(1,2-e)P 4,5-trtins-dihydrodiol and 12-OH-N(1,2-e)P on exposure of rat liver microsomes to N(1,2-e)P. The presence of N(1,2-e)P in the environment and formation of fjord region dihydrodiol 14 as a major metabolite in in vitro metabolism studies strongly suggest the role of N(1,2-e)P as a potential health hazard.

  16. Transcriptional Profiling of Dibenzo[def,p]chrysene-induced Spleen Atrophy Provides Mechanistic Insights into its Immunotoxicity in MutaMouse.

    Science.gov (United States)

    Chepelev, Nikolai L; Long, Alexandra S; Williams, Andrew; Kuo, Byron; Gagné, Rémi; Kennedy, Dean A; Phillips, David H; Arlt, Volker M; White, Paul A; Yauk, Carole L

    2016-01-01

    Dibenzo[def,p]chrysene (DBC) is the most carcinogenic polycyclic aromatic hydrocarbon (PAH) examined to date. We investigated the immunotoxicity of DBC, manifested as spleen atrophy, following acute exposure of adult MutaMouse males by oral gavage. Mice were exposed to 0, 2.0, 6.2, or 20.0 mg DBC /kg-bw per day, for 3 days. Genotoxic endpoints (DBC-DNA adducts and lacZ mutant frequency in spleen and bone marrow, and red blood cell micronucleus frequency) and global gene expression changes were measured. All of the genotoxicity measures increased in a dose-dependent manner in spleen and bone marrow. Gene expression analysis showed that DBC activates p53 signaling pathways related to cellular growth and proliferation, which was evident even at the low dose. Strikingly, the expression profiles of DBC exposed mouse spleens were highly inversely correlated with the expression profiles of the only published toxicogenomics dataset of enlarged mouse spleen. This analysis suggested a central role for Bnip3l, a pro-apoptotic protein involved in negative regulation of erythroid maturation. RT-PCR confirmed expression changes in several genes related to apoptosis, iron metabolism, and aryl hydrocarbon receptor signaling that are regulated in the opposite direction during spleen atrophy versus benzo[a]pyrene-mediated splenomegaly. In addition, benchmark dose modeling of toxicogenomics data yielded toxicity estimates that are very close to traditional toxicity endpoints. This work illustrates the power of toxicogenomics to reveal rich mechanistic information for immunotoxic compounds and its ability to provide information that is quantitatively similar to that derived from standard toxicity methods in health risk assessment. PMID:26496743

  17. Nanoparticle Self-Assembled Grain Like Curcumin Conjugated ZnO: Curcumin Conjugation Enhances Removal of Perylene, Fluoranthene, and Chrysene by ZnO

    Science.gov (United States)

    Moussawi, Rasha N.; Patra, Digambara

    2016-04-01

    Curcumin conjugated ZnO, referred as Zn(cur)O, nanostructures have been successfully synthesized, these sub-micro grain-like structures are actually self-assemblies of individual needle-shaped nanoparticles. The nanostructures as synthesized possess the wurtzite hexagonal crystal structure of ZnO and exhibit very good crystalline quality. FT-Raman and TGA analysis establish that Zn(cur)O is different from curcumin anchored ZnO (ZnO@cur), which is prepared by physically adsorbing curcumin on ZnO surfaces. Chemically Zn(cur)O is more stable than ZnO@cur. Diffuse reflectance spectroscopy indicates Zn(cur)O have more impurities compared to ZnO@cur. The solid-state photoluminescence of Zn(cur)O has been investigated, which demonstrates that increase of curcumin concentration in Zn(cur)O suppresses visible emission of ZnO prepared through the same method, this implies filling ZnO defects by curcumin. However, at excitation wavelength 425 nm the emission is dominated by fluorescence from curcumin. The study reveals that Zn(cur)O can remove to a far extent high concentrations of perylene, fluoranthene, and chrysene faster than ZnO. The removal depends on the extent of curcumin conjugation and is found to be faster for PAHs having smaller number of aromatic rings, particularly, it is exceptional for fluoranthene with 93% removal after 10 minutes in the present conditions. The high rate of removal is related to photo-degradation and a mechanism has been proposed.

  18. Nanoparticle Self-Assembled Grain Like Curcumin Conjugated ZnO: Curcumin Conjugation Enhances Removal of Perylene, Fluoranthene, and Chrysene by ZnO

    Science.gov (United States)

    Moussawi, Rasha N.; Patra, Digambara

    2016-01-01

    Curcumin conjugated ZnO, referred as Zn(cur)O, nanostructures have been successfully synthesized, these sub-micro grain-like structures are actually self-assemblies of individual needle-shaped nanoparticles. The nanostructures as synthesized possess the wurtzite hexagonal crystal structure of ZnO and exhibit very good crystalline quality. FT-Raman and TGA analysis establish that Zn(cur)O is different from curcumin anchored ZnO (ZnO@cur), which is prepared by physically adsorbing curcumin on ZnO surfaces. Chemically Zn(cur)O is more stable than ZnO@cur. Diffuse reflectance spectroscopy indicates Zn(cur)O have more impurities compared to ZnO@cur. The solid-state photoluminescence of Zn(cur)O has been investigated, which demonstrates that increase of curcumin concentration in Zn(cur)O suppresses visible emission of ZnO prepared through the same method, this implies filling ZnO defects by curcumin. However, at excitation wavelength 425 nm the emission is dominated by fluorescence from curcumin. The study reveals that Zn(cur)O can remove to a far extent high concentrations of perylene, fluoranthene, and chrysene faster than ZnO. The removal depends on the extent of curcumin conjugation and is found to be faster for PAHs having smaller number of aromatic rings, particularly, it is exceptional for fluoranthene with 93% removal after 10 minutes in the present conditions. The high rate of removal is related to photo-degradation and a mechanism has been proposed. PMID:27080002

  19. Analysis of dibenzo[def,p]chrysene-deoxyadenosine adducts in wild-type and cytochrome P450 1b1 knockout mice using stable-isotope dilution UHPLC-MS/MS.

    Science.gov (United States)

    Harper, Tod A; Morré, Jeff; Lauer, Fredine T; McQuistan, Tammie J; Hummel, Jessica M; Burchiel, Scott W; Williams, David E

    2015-04-01

    The polycyclic aromatic hydrocarbon (PAH), dibenzo[def,p]chrysene (DBC; also known as dibenzo[a,l]pyrene), is a potent carcinogen in animal models and a class 2A human carcinogen. Recent investigations into DBC-mediated toxicity identified DBC as a potent immunosuppressive agent similar to the well-studied immunotoxicant 7,12-dimethylbenz[a]anthracene (DMBA). DBC, like DMBA, is bioactivated by cytochrome P450 (CYP) 1B1 and forms the reactive metabolite DBC-11,12-diol-13,14-epoxide (DBCDE). DBCDE is largely responsible for the genotoxicity associated with DBC exposure. The immunosuppressive properties of several PAHs are also linked to genotoxic mechanisms. Therefore, this study was designed to identify DBCDE-DNA adduct formation in the spleen and thymus of wild-type and cytochrome P450 1b1 (Cyp1b1) knockout (KO) mice using a highly sensitive stable-isotope dilution UHPLC-MS/MS method. Stable-isotope dilution UHPLC-MS/MS identified the major DBC adducts (±)-anti-cis-DBCDE-dA and (±)-anti-trans-DBCDE-dA in the lung, liver, and spleen of both WT and Cyp1b1 KO mice. However, adduct formation in the thymus was below the level of quantitation for our method. Additionally, adduct formation in Cyp1b1 KO mice was significantly reduced compared to wild-type (WT) mice receiving DBC via oral gavage. In conclusion, the current study identifies for the first time DBCDE-dA adducts in the spleen of mice supporting the link between genotoxicity and immunosuppression, in addition to supporting previous studies identifying Cyp1b1 as the primary CYP involved in DBC bioactivation to DBCDE. The high levels of DBC-DNA adducts identified in the spleen, along with the known high levels of Cyp1b1 expression in this organ, supports further investigation into DBC-mediated immunotoxicity. PMID:25868132

  20. The influence of ATM, ATR, DNA-PK inhibitors on the cytotoxic and genotoxic effects of dibenzo[def,p]chrysene on human hepatocellular cancer cell line HepG2.

    Science.gov (United States)

    Spryszyńska, Sylwia; Smok-Pieniążek, Anna; Ferlińska, Magdalena; Roszak, Joanna; Nocuń, Marek; Stępnik, Maciej

    2015-09-01

    The effect of inhibitors of phosphatidylinositol-3-kinase related kinases (PIKK): ataxia-telangiectasia mutated (ATM), ATM- and Rad3-related (ATR) and DNA-dependent protein kinase (DNA-PK) on the response of HepG2 human liver cancer cells to dibenzo[def,p]chrysene (DBC) was investigated. High cytotoxicity of DBC (IC50=0.1μM) was observed after 72h incubation. PIKK inhibitors: KU55933 (5μM), NU7026 (10μM) or caffeine (1 and 2mM) when used alone did not significantly influence the cytotoxicity. However, two combinations: KU55933/NU7026 and caffeine/NU7026 significantly increased HepG2 viability (by 25%) after treatment with DBC at 0.5μM. The cytoprotective effect was confirmed by cell cycle and apoptosis/necrosis analysis. DNA damage level after exposure to DBC assessed by comet assay (single strand breaks) showed a long persistence and significant decrease after incubation of the cells in the presence the inhibitors (the combination of KU55933+NU7026 showed the strongest effect). Weak induction of reactive oxygen species (ROS) by DBC (0.5μM) was observed. Although, KU55933 and NU7026 when used alone did not increase ROS levels in the cells, their combination induced the ROS increase and moderately enhanced ROS generation by DBC. We propose a mechanism how cells with damaged DNA after exposure to DBC and under the condition of PIKK inhibition, may be at higher risk of undergoing malignant transformation. PMID:26338538

  1. From bifluorenylidene dianion to dibenzo[g,p]chrysene dianion: sensitivity of anisotropy changes to bonding structure

    DEFF Research Database (Denmark)

    Shenhar, R.; Beust, R.; Hagen, Stefan;

    2002-01-01

    Five polycyclic aromatic hydrocarbons of the C-26 series having similar bonding structure yield dianions upon reduction with lithium metal. Anisotropy changes, revealed from an advanced charge distribution analysis performed on these dianions, show a correlation to the bonding structure of the di......Five polycyclic aromatic hydrocarbons of the C-26 series having similar bonding structure yield dianions upon reduction with lithium metal. Anisotropy changes, revealed from an advanced charge distribution analysis performed on these dianions, show a correlation to the bonding structure...... calculation and experiment. The anisotropy change is suggested as a valid index for the reduction-induced change in the aromatic character of PAHs, which is applicable for both aromatic and anti-aromatic changes....

  2. Oxidation of PAHs in water solutions by ultraviolet radiation combined with hydrogen peroxide

    OpenAIRE

    Dorota Olejnik; Jacek S. Miller; Stanisław Ledakowicz

    1999-01-01

    The destruction of three polycyclic aromatic hydrocarbons (PAHs): benzo[a]pyrene, chrysene and fluorene in aqueous solution using advanced oxidation process H2O2/UV was investigated. The influence of pH, initial hydrogen peroxide and radical scavenger concentrations on the reaction rate was studied. The oxidation reactions most rapidly run in neutral and acidic solution at optimal hydrogen peroxide concentration (ca. 0.01 M). The degradation of benzo[a]pyrene and chrysene follows radical reac...

  3. 40 CFR 464.11 - Specialized definitions.

    Science.gov (United States)

    2010-07-01

    .... tetrachloroethylene 87. trichloroethylene (2) Die Casting (§ 464.15(c) and § 464.16(c)): 1. acenaphthene 4. benzene 7.... chrysene 78. anthracene 80. fluorene 81. phenanthrene 84. pyrene 85. tetrachloroethylene 86. toluene (3... (2-ethylhexyl) phthalate 84. pyrene 85. tetrachloroethylene 87. trichloroethylene (5) Melting...

  4. PROPOSED PROCEDURE FOR DERIVATION OF REGULATORY VALUES FOR CARCINOGENIC AIRBORNE POLYCYCLIC AROMATIC HYDROCARBONS (PAHS) BASED ON COAL TAR PITCH (CTP) VOLATILES

    Science.gov (United States)

    A procedure for estimating upper bound lifetime human cancer risk from air levels of 6 common carcinogenic PAHs, termed "PAHs of concern", is proposed. These PAHs are benzo(a)pyrene, benz(a)anathracene, benzo(k)flouranthene, indeno(1,2,3-c,d)pyrene and chrysene. In application,...

  5. Potential of glycerol and soybean oil for bioremediation of weathered oily-sludge contaminated soil

    Energy Technology Data Exchange (ETDEWEB)

    Nascimento, T.C.F.; Franca, F.P. [Universidade Federal do Rio de Janeiro (UFRJ), RJ (Brazil). Escola de Quimica], E-mail: fpfranca@eq.ufrj.br; Oliveira, F.J.S. [Petroleo Brasileiro S.A. (PETROBRAS), Rio de Janeiro, RJ (Brazil)

    2012-04-15

    The bioremediation of petroleum-contaminated soil was investigated on laboratory scale. This work evaluated the effect of co-substrate addition in tropical climate soil highly contaminated with oily residue. Glycerol and soybean oil were used as auxiliary co-substrates for contaminant degradation. Three different concentrations of co-substrate were tested, and the experiments were carried out over 60 days. The following parameters were monitored: humidity, pH, total heterotrophic bacteria, total fungi, total petroleum hydrocarbons (TPH), and the concentrations of benzo[a]pyrene and chrysene. The soil supplementation with renewable co-substrates improved the efficiency of the biodegradation TPH, with removals of 85% and 83% for glycerol and soybean oil, respectively, compared to a 55% removal yielded by the biodegradation process without supplementation. The use of glycerol increased Chrysene and Benzo[a]pyrene biodegradation by 50%, while soybean oil supplementation increased their removal by 36%. (author)

  6. 8,9-DIHYDROXY-8,9-DIHYDRODIBENZO[A,L]PYRENE IS A POTENT MORPHOLOGICAL CELL-TRANSFORMING AGENT IN C3H10T1/2C18 MOUSE EMBRYO FIBROBLASTS IN THE ABSENCE OF DETECTABLE STABLE COVALENT DNA ADDUCTS

    Science.gov (United States)

    The comparative genotoxic effects of racemic trans-8,9dihydroxy-8,9-dihydrodibenzo[a,l]pyrene (trans- DB[a,l]P8,9-diol), the metabolic K-region dihydrodiol of dibenzo[a,l] pyrene (DB[a,l]P) (dibenzo[def,p]chrysene) and DB[a,l]P in transformable mouse embryo C3HIOT1/2C18 (C3HIOT1/...

  7. 29 CFR 1915.1000 - Air contaminants.

    Science.gov (United States)

    2010-07-01

    ...)pyrene; see Coal tar pitch volatiles Benzoyl peroxide 94-36-0 — 5 — Benzyl chloride 100-44-7 1 5....1026 o Chromium metal and insol. salts (as Cr) 7440-47-3 — 1 — Chrysene; see Coal tar pitch volatiles Clopidol 2971-90-6 Total dust — 15 — Respirable fraction — 5 — Coal tar pitch volatiles (benzene...

  8. 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...

  9. Hydrostatic pressure effect on charge transport properties of phenacene organic semiconductors.

    Science.gov (United States)

    Nguyen, Thao P; Shim, Ji Hoon

    2016-05-18

    We investigate the charge transport properties of phenacene organic semiconductors including phenanthrene, chrysene and picene using density functional theory (DFT) calculations under hydrostatic pressure. Under compression, the crystal structures of the three materials are altered and thus, a decrease in the intermolecular distances gives changes in charge transport properties while the molecular structures remain stable. As a result of the applied pressure, the mobilities of these materials increase dramatically. Chrysene shows a transition from a p-type semiconductor to an ambipolar semiconductor at around 2.0 GPa. Interestingly, chrysene favors electron transport at above 3.0 GPa. On the other hand, both phenanthrene and picene exhibit hole transport characteristics under high pressure. Between 3.1 and 4.3 GPa, the picene crystal is found to transform from an anisotropic mobility to an isotropic mobility in the ab plane. We also found that, the bulk modulus representing the resistance of the material under pressure compression follows a linear relationship with molecular length. PMID:27146786

  10. 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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1988-07-01

    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-reactions between the benzo(a)pyrene and the chrysene diol-epoxide adducts were present. Similar cross-reactivity between the benz(a)anthracene and the chrysene adducts was observed. Sera containing antibodies that were apparently specific for each of the three PAH-DNA adducts were also identified. The presence of antibodies to PAH-DNA adducts indicates both past exposure to these carcinogenic PAH and their metabolic activation to the DNA damaging metabolites. These antibodies may prove to be useful in both retrospective and prospective epidemiological studies of various diseases associated with PAH exposure.

  12. Synthesis and Photoirradiation of Isomeric Ethylchrysenes by UVA Light Leading to Lipid Peroxidation

    Directory of Open Access Journals (Sweden)

    Peter P. Fu

    2007-06-01

    Full Text Available Polycyclic aromatic hydrocarbons (PAHs are widespread genotoxic environmental pollutants. We have recently demonstrated that photoirradiation of PAHs leads to cytotoxicity, DNA damage, and induction of lipid peroxidation. In this paper we report the synthesis of all the six isomeric ethylchrysenes and the study of light-induced lipid peroxidation by these ethylchrysenes. 5-Ethylchrysene was synthesized by reaction of 5-keto-5,6,6a,7,8,9,10,10a-octahydrochrysene with CH3CH2MgBr followed by dehydration catalyzed by p-toluenesulfonic acid and dehydrogenation with DDQ in benzene. 1- and 4-Ethylchrysenes were similarly prepared by reaction of 1-keto-1,2,3,4,5,6-hexahydrochrysene and 4-keto-1,2,3,4-tetrahydrochrysenes, respectively with CH3CH2MgBr followed by dehydration and dehydrogenation. Direct acetylation of chrysene followed by Wolff-Kishner or Clemmensen reduction resulted in the formation of 2-, 3-, and 6-ethylchrysenes in 4%, 16%, and 43% yields, respectively. Photoirradiation of these compounds with 7 and 21 J/cm2 UVA light in the presence of methyl linoleate all resulted in lipid peroxidation. For comparison, photoirradiation of 4-methylchrysene and 5-methylchrysene was similarly conducted. For irradiation at a UVA light dose of 21 J/cm2, the level of induced lipid peroxidation is in the order 4-methylchrysene = 5-methylchrysene = 5-ethylchrysene = 4-ethylchrysene = chrysene > 1-ethylchrysene = 2-ethylchrysene > 3-ethylchrysene > 6-ethylchrysene. Compared with chrysene, these results indicate that the ethyl group at C4 or C5 position either slightly enhances or has no effect on the light-induced lipid peroxidation, while at C1-, C2-, C3-, or C6 position reduces light-induced lipid peroxidation.

  13. Assessment of cancer and noncancer health risks from exposure to PAHs in street dust in the Tamale Metropolis, Ghana.

    Science.gov (United States)

    Obiri, Samuel; Cobbina, Samuel J; Armah, Frederick A; Luginaah, Isaac

    2013-01-01

    This study is part of a broader initiative to characterize, quantify and assess the human health risk associated with exposure to polycyclic aromatic hydrocarbons (PAHs) in street dust along the Trans-ECOWAS highway in West Africa. In the first part, PAHs were characterized and quantified in low- and high-traffic zones. In this study, cancer and noncancer human health risks from exposure to (PAHs) in street dust in the Tamale metropolis, Ghana were assessed in accordance with the USEPA risk assessment guidelines. The results of the study as obtained from inhalation of benzo [a] anthracene (BaA), benzo [a] pyrene (BaP), benzo [k] fluoranthene (BkF) and chrysene via central tendency exposure parameters (CTE) by trespassers (street hawkers including children and adults) in street dust within low traffic zones in the Tamale metropolis are 1.6E-02, 4.7E-02, 1.8E-03, and 1.6E-04 respectively. For reasonable maximum exposure parameters (RME), risk values of 1.2E-01, 3.5E-01, 1.3E-02 and 1.2E-03 respectively were obtained for benzo [a] anthracene, benzo [a] pyrene, benzo [k] fluoranthene and chrysene. Hazard index for acenaphthene, anthracene, fluoranthene, fluorine, naphthalene and pyrene in the CTE and RME scenarios were 2.2, 3.E-01, 2.6, 2.6, 100, 38 and 12, 1.7,15, 14, 550, 210 respectively. Generally, the cancer health risk associated with inhalation of benzo [a] anthracene, benzo [a] pyrene, benzo [k] fluoranthene and chrysene revealed that resident adults and children in the Tamale metropolis are at risk from exposure to these chemicals. The results of this preliminary assessment that quantified PAH related health risks along this part of the Trans-ECOWAS highway revealed that, there is the need for regulatory agencies to put in comprehensive measures to mitigate the risks posed to these categories of human receptors.

  14. Biomarkers of genotoxicity of air pollution (the AULIS project): bulky DNA adducts in subjects with moderate to low exposures to airborne polycyclic aromatic hydrocarbons and their relationship to environmental tobacco smoke and other parameters

    DEFF Research Database (Denmark)

    Georgiadis, P.; Topinka, J.; Stoikidou, M.;

    2001-01-01

    The levels of bulky DNA adducts were measured by (32)P-post-labelling in lymphocytes of 194 non-smoking students living in the city of Athens and the region of Halkida, Greece, once in the winter and again in the following summer. Personal exposures to particulate-bound polycyclic aromatic...... tobacco smoke (ETS), namely (i) declared times of exposure to ETS during the 24 h prior to blood donation, (ii) plasma cotinine levels and (iii) chrysene/benzo[g,h,i]perylene ratios in the profile of personal PAH exposure. Furthermore, among the Halkida campus area subjects (but not the remaining subjects...

  15. Oil pollution in the surface water of the Aegean Sea

    OpenAIRE

    Öztürk, Bayram; Güven, Kasim C.; Nesimigil, Filiz; Cumali, Selin; Dede, Ayhan

    2006-01-01

    Abstract Oil pollution in the surface water of the Aegean Sea was investigated from the Çanakkale Strait (Dardanelles) to the Marmaris Harbour, during 17-25 April in 2005. The oil pollution of samples was determined by UVF, through various crude oils and also chrysene as references materials. The oil pollution in water was ranged from 6.17 μg/L at Datca to 59.58 μg/L at Kusadasi through Russian crude oil equivalent. The highest polluted areas were Babakale-Kusadasi Bay, West of Giadoros Islan...

  16. Temperature Effects on Retention and Separation of PAHs in Reversed-Phase Liquid Chromatography Using Columns Packed with Fully Porous and Core-Shell Particles

    OpenAIRE

    Christophe Waterlot; Anaïs Goulas

    2016-01-01

    Effects of temperature on the reversed-phase chromatographic behavior of PAHs were investigated on three columns. The first was the recent C18 column (250 mm × 4.6 mm) packed with 5 µm core-shell particles while the others were more conventional C18 columns (250 mm × 4.6 mm) packed with fully porous particles. Among the 16 PAHs studied, special attention has been paid to two pairs of PAHs, fluorene/acenaphthene and chrysene/benzo[a]anthracene, which often present coeluting problems. Due to th...

  17. Structural Characterizations of Novel Non-Linear Poly aromatic Hydrocarbon Compounds

    OpenAIRE

    Mistry, Pooja Prakashkumar

    2015-01-01

    This thesis presents the structural characterisation of three, non-linear,polyaromatic hydrocarbons - chrysene and 4,10-dichlorochrysene and 4,10-dibromochrysene. 4,10-Dichlorochrysene and 4,10-dibromochrysenewere obtained from a novel benzannulation reaction of their respective 2,6-diallylnaphthalene-1,5-diyl bis(2,2,2-trihaloroacetates) - the “BHQ reaction”. Single crystal X-ray diffraction and X-ray powder diffraction studies on these compounds were conducted in order to determine the effe...

  18. 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

  19. Study to improve the bioavailability of polycyclic aromatic hydrocarbons (PAH). Ecological and toxicological evaluation of soils containing high PAH-concentration after biotechnological remediation (phase 1). Final report; Untersuchung zur Verbesserung der Bioverfuegbarkeit von polycyclischen aromatischen Kohlenwasserstoffen (PAH) und oekotoxikologische Bewertung biotechnologisch sanierter Boeden mit hohen PAH-Konzentrationen (Projektphase 1). Schlussbericht

    Energy Technology Data Exchange (ETDEWEB)

    Grimmer, G.; Jacob, J.; Dettbarn, G.; Raab, G.

    1995-10-25

    It shall be clarified in a pre-study (phase I), whether (1) stable metabolites arise from the decomposition of various PAH, which are enriched during the remediation process of soil, and (2) whether caffeine used to increase the bioavailablity of the PAH in the soil will be decomposed by the microorganism used in the remediation process. For the metabolic studies described here the fungus Mucor circinelloides was used. Pyrene, chrysene and benzo[a]pyrene are decomposed to hydroxylated derivatives by Mucor circinelloides. Investigations for the biochemical reaction kinetics are made. (orig./SR) [Deutsch] In einer Vorstudie (Phase 1) soll geklaert werden, ob (1) stabile Stoffwechselprodukte beim Abbau der einzelnen PAH entstehen, die sich bei der Bodensanierung anreichern und (2) das zur Verbesserung der Bioverfuegbarkeit der PAH in den Boden eingebrachte Coffein durch die verwendeten Mikroorganismen abgebaut wird. Fuer die hier beschriebenen Stoffwechseluntersuchungen wurde der Pilz Mucor circinelloides verwendet. Pyren, Chrysen und Benzo[a]pyren werden durch Mucor circinelloides zu hydroxylierten Derivaten abgebaut. Fuer den biologischen Abbau wurden Unterscuhungen zur Kinetik durchgefuehrt. (orig./SR)

  20. Gas chromatography-mass spectrometric determination of polycyclic aromatic hydrocarbons in five species of fish from three sites in the Arabian Gulf.

    Science.gov (United States)

    Al-Saleh, Iman; Al-Doush, Inaam

    2002-06-01

    A gas chromatography-mass spectrmetroic (GC-MS) method was developed to measure six polycyclic aromatic hydrocarbons (PAHs) in 54 fish samples. Five fish species highly consumed by the local population (shrimps, Emperors, Rabbitfish, Doublebar Bream and Greasy Grouper) were selected from three different sites on the Gulf coast of Saudi Arabia where agricultural, municipal and petroleum industry activities take place. Variations in PAH levels among the three sites were not significant. Total concentrations of PAHs benzo(a)anthracene, chrysene, and benzo(b)fluoranthene ranged from non-detectable to 44.9 microg kg(-1). In this study, concentrations of benzo(a)anthracene, chrysene, benzo(b)fluoranthene and total PAHs greater than the acceptable tolerance limit (1 microg kg(-1)) were found in 68.5, 40.7, 51.9 and 83.3% of the fish samples, respectively. PAH contents in fish vary considerably with species; Doublebar bream contain the highest while shrimps contain the lowest. This pilot study clearly shows that the consumption of fish could be a source of exposure of the local population to PAHs. Since there is a consensus on the substantial contribution of PAHs to cancer in humans, it would be interesting to conduct further research in order to determine the magnitude of the problem along other coastal regions of Saudi Arabia.

  1. [Appearance of aromatic polycyclic hydrocarbons during construction of asphalt and tar road surfaces].

    Science.gov (United States)

    Braszczyńska, Z; Osińska, R; Linscheid, D; Smolik, E

    1987-01-01

    The dust was sampled using personal samplers and stationary aspirators. PAHs were determined by thin layer chromatography and spectrophotometry in the UV and Vis range. In the samples the concentrations of coal tar pitch volatiles (benzene extract) and phenanthrene, fluoranthene, pyrene, chrysene, tetraphene, benzo(a)pyrene, benzo(e)pyrene, perylene, 1,12 benzoperylene, indeno(1,2,3-cd) pyrene were determined. The qualitative analysis identified all these hydrocarbons but only fluoranthene, pyrene, chrysene, tetraphene and benzo(a)pyrene could be quantitatively determined. The benzene extract concentration exceeds the value of 0.2 mg/m3 in 50% of samples. Much higher results were obtained for tar-concrete (1.45-2.85 mg/m3) than for asphalt-concrete (0.14-0.71 mg/m3). Also the drivers are exposed to excess benzene extract concentrations (0.055-0.669 mg/m3). Laboratory workers were found to be exposed to high concentrations of PAH and several solvents.

  2. Effect-directed analysis and mixture effects of AhR-active PAHs in crude oil and coastal sediments contaminated by the Hebei Spirit oil spill.

    Science.gov (United States)

    Hong, Seongjin; Lee, Sangwoo; Choi, Kyungho; Kim, Gi Beum; Ha, Sung Yong; Kwon, Bong-Oh; Ryu, Jongseong; Yim, Un Hyuk; Shim, Won Joon; Jung, Jinho; Giesy, John P; Khim, Jong Seong

    2015-04-01

    The major AhR-active PAHs were identified in crude oil and oil-contaminated sediments by use of effect-directed analysis. As part of the study, an enhanced potency balance analysis was conducted by establishing the novel relative potency values of (alkyl)-PAHs from the H4IIE-luc bioassay. Silica gel column fractionation of crude oil resulted in greater AhR-mediated potencies in fractions of aromatics (F2) and resins (F3), and such trend was also observed for field collected sediment samples. AhR-mediated potencies of six F2 sub-fractions from HPLC indicated that the majority of F2 responses were attributable to 3-4 ring aromatics. Target PAHs including C4-phenanthrene, C1-chrysene, and C3-chrysene in sediments explained ∼ 18% of the bioassay-derived TCDD-EQs, however, the unknown AhR agonists and potential mixture effects remain in question. Overall, the AhR-potency and antagonistic potential of residual oil in sediment tended to decrease over time, thus monitoring of weathering process would be key for the post management of oil-contaminated sites.

  3. Embryotoxic and teratogenic effects of petroleum hydrocarbons in mallards (Anas platyrhynchos)

    Science.gov (United States)

    Hoffman, D.J.

    1979-01-01

    Egg surface applications of microliter quantities of crude and refined oils of high aromatic content are embryotoxic to mallards (Anas platyrhynchos) and other avian species; applications of aliphatic hydrocarbons have virtually no effect. Mallard eggs at 72 h of development were exposed to a mixture of aromatic hydrocarbons or to aromatic compounds representative to those present in crude oil to assess their toxicity. The class composition of the mixture was similar to that of South Louisiana crude oil, an American Petroleum Institute reference oil. Application of 20 microliter of the mixture reduced embryonic survival by nearly 70%. The temporal pattern of embryonic death was similar to that after exposure to South Louisiana crude oil. Embryonic growth was stunted, as reflected by weight, crown-rump length, and bill length, and there was a significant increase in the incidence of abnormal survivors. When individual classes of aromatic hydrocarbons were tested, tetracyclics caused some embryonic death at the concentrations in the mixture. When classes were tested in all possible combinations of two, no combination appeared to be as toxic as the entire mixture. Addition of the tetracyclic compound chrysene to the aromatic mixture considerably enhanced embryotoxicity, but could not completely account for the toxicity of the crude oil. The presence of additional unidentified polycyclic aromatic hydrocarbons as well as methylated derivatives of polycyclic aromatic compounds such as chrysene may further account for the embryotoxicity of the crude oil.

  4. Embryotoxic and teratogenic effects of petroleum hydrocarbons in mallards (Anas platyrhynchos).

    Science.gov (United States)

    Hoffman, D J

    1979-09-01

    Egg surface applications of microliter quantities of crude and refined oils of high aromatic content are embryotoxic to mallards (Anas platyrhynchos) and other avian species; applications of aliphatic hydrocarbons have virtually no effect. Mallard eggs at 72 h of development were exposed to a mixture of aromatic hydrocarbons or to aromatic compounds representative to those present in crude oil to assess their toxicity. The class composition of the mixture was similar to that of South Louisiana crude oil, an American Petroleum Institute reference oil. Application of 20 microliter of the mixture reduced embryonic survival by nearly 70%. The temporal pattern of embryonic death was similar to that after exposure to South Louisiana crude oil. Embryonic growth was stunted, as reflected by weight, crown-rump length, and bill length, and there was a significant increase in the incidence of abnormal survivors. When individual classes of aromatic hydrocarbons were tested, tetracyclics caused some embryonic death at the concentrations in the mixture. When classes were tested in all possible combinations of two, no combination appeared to be as toxic as the entire mixture. Addition of the tetracyclic compound chrysene to the aromatic mixture considerably enhanced embryotoxicity, but could not completely account for the toxicity of the crude oil. The presence of additional unidentified polycyclic aromatic hydrocarbons as well as methylated derivatives of polycyclic aromatic compounds such as chrysene may further account for the embryotoxicity of the crude oil. PMID:513150

  5. Highly selective detection of oil spill polycyclic aromatic hydrocarbons using molecularly imprinted polymers for marine ecosystems.

    Science.gov (United States)

    Krupadam, Reddithota J; Nesterov, Evgueni E; Spivak, David A

    2014-06-15

    Im*plications due to oil spills on marine ecosystems have created a great interest toward developing more efficient and selective materials for oil spill toxins detection and remediation. This research paper highlights the application of highly efficient molecularly imprinted polymer (MIP) adsorbents based on a newly developed functional crosslinker (N,O-bismethacryloyl ethanolamine, NOBE) for detection of highly toxic polycyclic aromatic hydrocarbons (PAHs) in seawater. The binding capacity of MIP for oil spill toxin pyrene is 35 mg/g as compared to the value of 3.65 mg/g obtained using a non-imprinted polymer (NIP). The selectivity of all three high molecular weight PAHs (pyrene, chrysene and benzo[a]pyrene) on the NOBE-MIP shows an excellent selective binding with only 5.5% and 7% cross-reactivity for chrysene and benzo[a]pyrene, respectively. Not only is this particularly significant because the rebinding solvent is water, which is known to promote non-selective hydrophobic interactions; the binding remains comparable under salt-water conditions. These selective and high capacity adsorbents will find wide application in industrial and marine water monitoring/remediation.

  6. Characterization of polycyclic aromatic hydrocarbons in fugitive PM10 emissions from an integrated iron and steel plant.

    Science.gov (United States)

    Khaparde, V V; Bhanarkar, A D; Majumdar, Deepanjan; Rao, C V Chalapati

    2016-08-15

    Fugitive emissions of PM10 (particles <10μm in diameter) and associated polycyclic aromatic hydrocarbons (PAHs) were monitored in the vicinity of coking unit, sintering unit, blast furnace and steel manufacturing unit in an integrated iron and steel plant situated in India. Concentrations of PM10, PM10-bound total PAHs, benzo (a) pyrene, carcinogenic PAHs and combustion PAHs were found to be highest around the sintering unit. Concentrations of 3-ring and 4-ring PAHs were recorded to be highest in the coking unit whereas 5-and 6-ring PAHs were found to be highest in other units. The following indicatory PAHs were identified: indeno (1,2,3-cd) pyrene, dibenzo (a,h) anthracene, benzo (k) fluoranthene in blast furnace unit; indeno (1,2,3-cd) pyrene, dibenzo (a,h) anthracene, chrysene in sintering unit; Anthracene, fluoranthene, chrysene in coking unit and acenaphthene, fluoranthene, fluorene in steel making unit. Total-BaP-TEQ (Total BaP toxic equivalent quotient) and BaP-MEQ (Total BaP mutagenic equivalent quotient) concentration levels ranged from 2.4 to 231.7ng/m(3) and 1.9 to 175.8ng/m(3), respectively. BaP and DbA (dibenzo (a,h) anthracene) contribution to total-BaP-TEQ was found to be the highest. PMID:27099996

  7. Hydroxypropyl cyclic β-(1 → 2)-D-glucans and epichlorohydrin β-cyclodextrin dimers as effective carbohydrate-solubilizers for polycyclic aromatic hydrocarbons.

    Science.gov (United States)

    Choi, Jae Min; Jeong, Daham; Piao, Jinglan; Kim, Kyoungtea; Nguyen, Andrew Bao Loc; Kwon, Nak-Jung; Lee, Mi-Kyung; Lee, Im Soon; Yu, Jae-Hyuk; Jung, Seunho

    2015-01-12

    The removal of polycyclic aromatic hydrocarbons by soil washing using water is extremely difficult due to their intrinsic hydrophobic nature. In this study, the effective aqueous solubility enhancements of seven polycyclic aromatic hydrocarbons by chemically modified hydroxypropyl rhizobial cyclic β-(1 → 2)-D-glucans and epichlorohydrin β-cyclodextrin dimer have been investigated for the first time. In the presence of hydroxypropyl cyclic β-(1 → 2)-D-glucans, the solubility of benzo[a]pyrene is increased up to 38 fold of its native solubility. The solubility of pyrene and phenanthrene dramatically increased up to 160 and 359. Coronene, chrysene, perylene, and fluoranthene also show an increase of 11, 23, 23, and 97 fold, respectively, of enhanced solubility by complexation with synthetic epichlorohydrin β-cyclodextrin dimer. The physicochemical properties of the complex are characterized by Fourier-transform infrared spectra and differential scanning calorimetry. Utilizing a scanning electron microscopy, the morphological structures of native benzo[a]pyrene, pyrene, phenanthrene, coronene, chrysene, perylene, fluoranthene and their complex with novel carbohydrate-solubilizers are studied. These results elucidate that polycyclic aromatic hydrocarbons are able to form an efficient complex with hydroxypropyl cyclic β-(1 → 2)-D-glucans and β-cyclodextrin dimer, suggesting the potential usage of chemically modified novel carbohydrate-solubilizers.

  8. Determination of polycyclic aromatic hydrocarbons in smoked and non-smoked black teas and tea infusions.

    Science.gov (United States)

    Pincemaille, Justine; Schummer, Claude; Heinen, Eric; Moris, Gilbert

    2014-02-15

    This study describes the occurrence of polycyclic aromatic hydrocarbons (PAHs) in smoked tea and tea infusions, via the monitoring of benzo(a)anthracene, chrysene, benzo(b)fluoranthene and benzo(a)pyrene (PAH4) that have been chosen as indicators for the occurrence of PAHs in food by the European Food Safety Agency. The concentrations ranged from 1.2 μg/kg for benzo(b)fluoranthene to 125.0 μg/kg for benzo(a)anthracene in smoked tea leaves, and from 0.6 μg/L for benzo(a)anthracene to 1.2 μg/L for benzo(b)fluoranthene in smoked tea infusions. Benzo(a)pyrene was never detected in infusions. The concentrations in non-smoked tea leaves ranged from 0.6 μg/kg for benzo(a)anthracene to 10.8 μg/kg for benzo(b)fluoranthene. It was shown that the concentrations of benzo(a)anthracene and chrysene were higher in smoked tea than in non-smoked tea while no difference was observed for benzo(b)fluoranthene and benzo(a)pyrene. The concentrations of PAHs in tea infusions are low compared to other foodstuffs, but the migration rates from leaves into water are high (82-123%).

  9. Contamination of agricultural lands by polycyclic aromatic hydrocarbons (Tver region, Russia)

    Science.gov (United States)

    Zhidkin, Andrey; Koshovskii, Timur; Gennadiev, Alexander

    2016-04-01

    It is important to study sources and concentrations of polycyclic aromatic hydrocarbons (PAHs) in the agriculture soils within areas without intensive contaminations. Our studied object was soil and snow cover in the taiga zone (Tver region, Russia). A total of 52 surface (0-30 cm) and 31 subsurface (30-50 cm) soil samples, and 13 snow samples were collected in 35 soil pits, located in forest, crop and layland soils. Studied concentrations of the following 11 individual compounds: two-ring compounds (diphenyl and naphthalene homologues); three-ring compounds (fluorene, phenanthrene, anthracene); four-ring compounds (chrysene, pyrene, tetraphene); five-ring compounds (perylene, benzo[a]pyrene); and six-ring compounds (benzo[ghi]perylene). Analyses made by specrtofluorometry method at the temperature of liquid nitrogen. The total concentrations of all PAHs in soil samples ranged from 9 to 770 ng*g‑1 with a median of 96 ng*g‑1. The sum of high molecular weight PAHs was significantly lower than the sum of low molecular weight PAHs in the studied soils. The phenanthrene concentration was highest and ranged from 1.2 to 720 ng*g‑1 (medium 72 ng*g‑1). Compared PAHs reserves in snow cover (μg*m-2) with the reserves in topsoil layer (μg*m-2 in the upper 30 cm). Low molecular weight PAHs (fluorene, phenanthrene, diphenyl, naphthalene) reserves in snow was less than 20% from the reserves in the soil surface layer. High molecular weight PAHs (benzo[a]pyrene, chrysene, perylene, pyrene and tetraphene) reserves in snow was about 50-70% from the reserves in soil surface layer. High molecular weight PAHs (benzo[ghi]perylene and anthracene) reserves in snow was more than in topsoil. PAHs vertical distribution in soil profiles was statistically examined. The total concentration of all PAHs decreased with depth in all studied forest soils. In the arable soils was no significant trend in domination of PAHs total concentrations in the plowing and subsoil layers. The ratio of

  10. Biodegradation of petroleum-based oil wastes through composting.

    Science.gov (United States)

    Kirchmann, H; Ewnetu, W

    1998-01-01

    Composting of horse manure was used as a means of degradation of two oil wastes, oil sludge from petrol stations and petroleum residues from a refinery. Paraffin oil was chosen as a reference. Oil wastes decomposed to 78-93% during 4.5 months of composting. The degradation of the waste oils was higher than that of the reference paraffin oil and no difference was found between the two types of oil wastes concerning their decomposition. At the end of the experiment, most of the polyaromatic hydrocarbons had been degraded except pyrene, chrysene and dibenz(ah)anthracene. Gaseous losses of oil compounds through volatilisation from composts were found not to be significant.

  11. Filtration d’une huile dopée avec quatre hydrocarbures aromatiques polycycliques (HAP sur des plaques garnies en charbon actif

    Directory of Open Access Journals (Sweden)

    Sidani Marion

    2012-11-01

    Full Text Available Powdered activated carbon is used in oils and fats refining to bleach and purify vegetable oils and fish oils. Actually, this powder makes it possible to detoxify crude fish oils and to eliminate contaminants like PAH, dioxin and PCB. Nevertheless, the powdered activated carbon used is painful because it is pulverulent. Nowadays, producers advise filtration plates filled with this powder. The aim of this study is to check the efficiency of such plates in the PAH elimination and verify the respect of the new 2011 regulation (2 μg/kg for benzo(apyrene, 10 μg/kg for the sum of benzo(apyrene, benzo(bfluoranthene, benzo (aanthracene and chrysene.

  12. Comparison of PCBs and PAHs levels in European coastal waters using mussels from the Mytilus edulis complex as biomonitors

    Directory of Open Access Journals (Sweden)

    Michał Olenycz

    2015-04-01

    Full Text Available Mussels from the Mytilus edulis complex were used as biomonitors for two groups of organic pollutants: polychlorinated biphenyls (PCBs, congeners: 28, 52, 101, 118, 138, 153 and 180 and polycyclic aromatic hydrocarbons (PAHs, naphthalene, acenaphthylene, acenaphthene, fluorene, phenanthrene, anthracene, fluoranthene, pyrene, benz(aanthracene, chrysene, benzo(bfluoranthene, benzo(kfluoranthene, benzo(apyrene, indeno(1,2,3-cdpyrene, dibenz(a,hanthracene, benzo(g,h,iperylene at 17 sampling sites to assess their relative bioavailabilities in coastal waters around Europe. Because of the temporal differences in PCBs and PAHs concentrations, data were adjusted using Seasonal Variation Coefficients (SVC before making large-scale spatial comparisons. The highest concentrations of PCBs were found near estuaries of large rivers flowing through urban areas and industrial regions. Elevated bioavailabilities of PAHs occurred in the vicinity of large harbors, urban areas, and regions affected by petroleum pollution as well as in some remote locations, which indicated long-range atmospheric deposition.

  13. The biodegradation of crude oil in the deep ocean.

    Science.gov (United States)

    Prince, Roger C; Nash, Gordon W; Hill, Stephen J

    2016-10-15

    Oil biodegradation at a simulated depth of 1500m was studied in a high-pressure apparatus at 5°C, using natural seawater with its indigenous microbes, and 3ppm of an oil with dispersant added at a dispersant:oil ratio of 1:15. Biodegradation of the detectable hydrocarbons was prompt and extensive (>70% in 35days), although slower by about a third than under otherwise identical conditions equivalent to the surface. The apparent half-life of biodegradation of the total detectable hydrocarbons at 15MPa was 16days (compared to 13days at atmospheric pressure), although some compounds, such as the four-ring aromatic chrysene, were degraded rather more slowly.

  14. PAHs in corn grains submitted to drying with firewood.

    Science.gov (United States)

    de Lima, Rafael Friedrich; Dionello, Rafael Gomes; Peralba, Maria do Carmo Ruaro; Barrionuevo, Simone; Radunz, Lauri Lourenço; Reichert Júnior, Francisco Wilson

    2017-01-15

    Grain drying using firewood as fuel for air heating, with direct fire, is still widely used in Brazil. The combustion of organic material, such as wood, can generate polycyclic aromatic hydrocarbons (PAHs) which are known to have carcinogenic potential. In the present work corn grain drying was carried out at three drying air temperatures: 60°C, 60/80°C and 80°C. Following the drying process, the presence and quantification of PAH in the corn grains was investigated. After extracting the PAHs of the matrix, the material was subjected to analysis by gas chromatography with mass detector. he results showed the presence of seven compounds: fluorene, phenanthrene, anthracene, fluoranthene, pyrene, benzo(a)anthracene and chrysene. PMID:27542463

  15. Determination of polyaromatic hydrocarbons in domestic, commercial and industrial soot samples

    Energy Technology Data Exchange (ETDEWEB)

    Iqbal, Yousaf; Sohail, Syed Muhammad; Ahmad, Imtiaz [Peshawar Univ., Khyber Pakhtunkhawa (Pakistan). Inst. of Chemical Sciences; Saeed, Khalid [Malakand Univ., Khyber Pakhtunkhawa (Pakistan). Dept. of Chemistry

    2013-05-15

    Polycyclic aromatic hydrocarbons (PAHs) were determined in domestic, commercial and industrial soot samples via HPLC. The study showed that benzo[a]pyrene (bap) was not present in most of the samples. The highest quantity of BaP was found in Pakistan Particle Board where its concentration was 259.12 mg/kg. The high quantity of other PAHs such as chrysene (CHR), anthracene (ANT), fluorene (FL), naphthalene (NAP), phenanthrene (PHE), acenaphthylene (ACP) and flouranthene (FTH) were found in tandoor, kabab karayi, tabakhee, brick kiln and motor car soot samples. The low concentration of most of the PAH compounds in most of the samples might be due to their photooxidative, biological and microbial degradation. (orig.)

  16. Induction of active melanocytes in mouse skin by carcinogens: a new method for detection of skin carcinogens.

    Science.gov (United States)

    Iwata, K; Inui, N; Takeuchi, T

    1981-01-01

    Application of potent skin carcinogens, such as 7,12-dimethylbenz[a]anthracene, 3-methylcholanthrene, benzo[a]pyrene and 4-nitroquinoline-1-oxide, induced numerous dihydroxyphenylalanine (dopa)-positive cells in the interfollicular epidermis of C57BL/6 mice in a dose- and time-dependent fashion. Chrysene, a weak skin carcinogen, and croton oil, a tumor promoter, also induced 3--4 times more dopa-positive cells than acetone. Liver carcinogens, such as 3'-methyl-4-dimethylaminoazobenzene and N-2-acetylaminofluorene, and non-carcinogenic aromatic hydrocarbons, such as anthracene, fluoranthene, fluorene and pyrene, did not induce increase in these cells. These results indicate that increase in the number of dopa-positive cells after application of chemicals is well correlated with the abilities of these compounds to induce skin carcinogenesis and suppress sebaceous glands. PMID:7273337

  17. Monitoring of PAHs and alkylated PAHs in aquatic organisms after 1 month from the Solar I oil spill off the coast of Guimaras Island, Philippines.

    Science.gov (United States)

    Uno, Seiichi; Koyama, Jiro; Kokushi, Emiko; Monteclaro, Harold; Santander, Sheryll; Cheikyula, J Orkuma; Miki, Shizuho; Añasco, Nathaniel; Pahila, Ida G; Taberna, Hilario S; Matsuoka, Tatsuro

    2010-06-01

    Following the oil spill accident of the Solar I tanker in 2006 off the coast of Guimaras Island in the Philippines, polycyclic aromatic hydrocarbons (PAHs) and alkylated PAHs in some aquatic organisms were investigated at Luzaran in Guimaras and Taklong Islands, which were heavily polluted with spilled oil, immediately and 1 month after the accident. The concentrations of total PAHs were 11.9-52.3 ng/g dry weight in fish. Meanwhile, total PAH concentrations in shellfish were 38.0-3,102 ng/g dry weight in Luzaran and 128-236 ng/g dry weight in Taklong. Pyrene, phenanthrene, and fluoranthene were dominant in most fish and chrysene in all shellfish. Significantly higher concentrations of all alkylated homologs were detected in shellfish than in fish. These differences had two possible causes, that is, the differences between fish and shellfish could be attributed to the uptake routes and/or their metabolizing abilities.

  18. High-resolution IR absorption spectroscopy of polycyclic aromatic hydrocarbons in the 3 {\\mu}m region: Role of periphery

    CERN Document Server

    Maltseva, Elena; Candian, Alessandra; Mackie, Cameron J; Huang, Xinchuan; Lee, Timothy J; Tielens, Alexander G G M; Buma, Wybren Jan

    2016-01-01

    In this work we report on high-resolution IR absorption studies that provide a detailed view on how the peripheral structure of irregular polycyclic aromatic hydrocarbons (PAHs) affects the shape and position of their 3 {\\mu}m absorption band. To this purpose we present mass-selected, high-resolution absorption spectra of cold and isolated phenanthrene, pyrene, benz[a]antracene, chrysene, triphenylene, and perylene molecules in the 2950-3150 cm-1 range. The experimental spectra are compared with standard harmonic calculations, and anharmonic calculations using a modified version of the SPECTRO program that incorporates a Fermi resonance treatment utilizing intensity redistribution. We show that the 3 {\\mu}m region is dominated by the effects of anharmonicity, resulting in many more bands than would have been expected in a purely harmonic approximation. Importantly, we find that anharmonic spectra as calculated by SPECTRO are in good agreement with the experimental spectra. Together with previously reported hi...

  19. Content comparison of polycyclic aromatic hydrocarbons (PAHs in traditionally smoked freshwater fish

    Directory of Open Access Journals (Sweden)

    Renata Pietrzak-Fiećko

    2015-09-01

    Full Text Available The aim of this study was to compare the content of chosen PAHs (benzo[a]pyrene, benzo[a]anthracene, chrysene, benzo[b]fluoranthene in meat of different freshwater fish species that were traditionally (directly smoked. The survey covered 16 freshwater fish samples of four species: rainbow trout (Oncorhynchus mykiss, carp (Cyprinus carpio, vendace (Coregonus albula and eel (Anguilla anguilla. Average content of sum of four PAHs in meat of trout, carp, vendace and eel was: 2.73, 8.23, 6.45 and 3.65 µg/kg of meat, respectively. Maximum levels of chosen PAHs in meat of examined fish species were not exceeded by any of the samples. Conducted studies confirmed that meat of traditionally smoked trout, carp, vendace and eel is safe in terms of content of the analysed PAHs.

  20. Photodegradation of PAHs in passive water samplers.

    Science.gov (United States)

    Allan, Ian J; Christensen, Guttorm; Bæk, Kine; Evenset, Anita

    2016-04-15

    Losses of deuterated polycyclic aromatic hydrocarbons (PAHs) used as performance reference compounds (PRCs) in semipermeable membrane devices deployed at fifteen coastal sampling sites near Harstad harbour in Northern Norway were used to investigate photodegradation of these photosensitive compounds. Unusual PRC dissipation profiles, especially for samplers exposed <5m below the water surface are indicative of photodegradation. A strong correlation between loss rates for d12-chrysene and d12-benzo[e]pyrene with consistently higher losses of the latter was found. The observed photodegradation rates may be sufficiently high to impact PAH masses absorbed by a factor of two. This study demonstrates that photodegradation during exposure of passive water samplers needs to be taken into account, particularly with deployments close to the water surface, when using SPMD canisters, or when sampling in the Arctic. PMID:26876557

  1. Biodegradation of naphthalene and anthracene by chemo-tactically active rhizobacteria of populus deltoides

    Directory of Open Access Journals (Sweden)

    Sandeep Bisht

    2010-12-01

    Full Text Available Several naphthalene and anthracene degrading bacteria were isolated from rhizosphere of Populus deltoides, which were growing in non-contaminated soil. Among these, four isolates, i.e. Kurthia sp., Micrococcus varians, Deinococcus radiodurans and Bacillus circulans utilized chrysene, benzene, toluene and xylene, in addition to anthracene and naphthalene. Kurthia sp and B. circulans showed positive chemotactic response for naphthalene and anthracene. The mean growth rate constant (K of isolates were found to increase with successive increase in substrate concentration (0.5 to 1.0 mg/50ml. B. circulans SBA12 and Kurthia SBA4 degraded 87.5% and 86.6% of anthracene while, Kurthia sp. SBA4, B. circulans SBA12, and M. varians SBA8 degraded 85.3 %, 95.8 % and 86.8 % of naphthalene respectively after 6 days of incubation as determined by HPLC analysis.

  2. Phytoremediation of mixed-contaminated soil using the hyperaccumulator plant Alyssum lesbiacum: evidence of histidine as a measure of phytoextractable nickel.

    Science.gov (United States)

    Singer, Andrew C; Bell, Thomas; Heywood, Chloe A; Smith, J A C; Thompson, Ian P

    2007-05-01

    In this study we examine the effects of polycyclic aromatic hydrocarbons (PAHs) on the ability of the hyperaccumulator plant Alyssum lesbiacum to phytoextract nickel from co-contaminated soil. Planted and unplanted mesocosms containing the contaminated soils were repeatedly amended with sorbitan trioleate, salicylic acid and histidine in various combinations to enhance the degradation of two PAHs (phenanthrene and chrysene) and increase nickel phytoextraction. Plant growth was negatively affected by PAHs; however, there was no significant effect on the phytoextraction of Ni per unit biomass of shoot. Exogenous histidine did not increase nickel phytoextraction, but the histidine-extractable fraction of soil nickel showed a high correlation with phytoextractable nickel. These results indicate that Alyssum lesbiacum might be effective in phytoextracting nickel from marginally PAH-contaminated soils. In addition, we provide evidence for the broader applicability of histidine for quantifying and predicting Ni phytoavailability in soils. PMID:17084494

  3. 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.

  4. Modeling of experimental data on trace elements and organic compounds content in industrial waste dumps.

    Science.gov (United States)

    Smoliński, Adam; Drobek, Leszek; Dombek, Václav; Bąk, Andrzej

    2016-11-01

    The main objective of the study presented was to investigate the differences between 20 mine waste dumps located in the Silesian Region of Poland and Czech Republic, in terms of trace elements and polycyclic aromatic hydrocarbons contents. The Principal Component Analysis and Hierarchical Clustering Analysis were applied in exploration of the studied data. Since the data set was affected by outlying objects, the employment of a relevant analysis strategy was necessary. The final PCA model was constructed with the use of the Expectation-Maximization iterative approach preceded by a correct identification of outliers. The analysis of the experimental data indicated that three mine waste dumps located in Poland were characterized by the highest concentrations of dibenzo(g,h,i)anthracene and benzo(g,h,i)perylene, and six objects located in Czech Republic and three objects in Poland were distinguished by high concentrations of chrysene and indeno (1.2.3-cd) pyrene. Three of studied mine waste dumps, one located in Czech Republic and two in Poland, were characterized by low concentrations of Cr, Ni, V, naphthalene, acenaphthene, fluorene, phenanthrene, anthracene, fluoranthen, benzo(a)anthracene, chrysene, benzo (b) fluoranthene, benzo (k) fluoranthene, benzo(a)pyrene, dibenzo(g,h,i)anthracene, benzo(g,h,i)perylene and indeno (1.2.3-cd) pyrene in comparison with the remaining ones. The analysis contributes to the assessment and prognosis of ecological and health risks related to the emission of trace elements and organic compounds (PAHs) from the waste dumps examined. No previous research of similar scope and aims has been reported for the area concerned. PMID:27497349

  5. Hard Cap Espresso Machines in Analytical Chemistry: What Else?

    Science.gov (United States)

    Armenta, Sergio; de la Guardia, Miguel; Esteve-Turrillas, Francesc A

    2016-06-21

    A hard cap espresso machine has been used in combination with liquid chromatography with molecular fluorescence detection for the determination of polycyclic aromatic hydrocarbons (PAHs) from contaminated soils and sediments providing appropriate extraction efficiencies and quantitative results. Naphthalene, acenaphthene, fluorene, phenanthrene, anthracene, fluoranthene, pyrene, benz[a]anthracene, chrysene, benz[b]fluoranthene, benz[k]fluoranthene, benz[a]pyrene, dibenz[a,h]anthracene, benz[ghi]perylene, and indeno[1,2,3-cd]pyrene were used as target compounds. It should be mentioned that the pairs benz[a]anthracene-chrysene and dibenz[a,h]anthracene-benz[ghi]perylene peaks coelute under the employed chromatographic conditions; thus, those compounds were determined together. PAHs were extracted from 5.0 g of soil, previously homogenized, freeze-dried, and sieved to 250 μm, with 50 mL of 40% (v/v) acetonitrile in water at a temperature of 72 ± 3 °C. The proposed procedure is really fast, with an extraction time of 11 s, and it reduces the required amount of organic solvent to do the sample preparation. The obtained limit of detection for the evaluated PAHs was from 1 to 38 μg kg(-1). Recoveries were calculated using clean soils spiked with 100, 500, 1000, and 2000 μg kg(-1) PAHs with values ranging from 81 to 121% and good precision with relative standard deviation values lower than 30%. The method was validated using soil and sediment certified reference materials and also using real samples by comparison with ultrasound-assisted extraction, as reference methodology, obtaining statistically comparable results. Thus, the use of hard cap espresso machines in the analytical laboratories offers tremendous possibilities as low cost extraction units for the extraction of solid samples. PMID:27224000

  6. Bioaccessibility of AhR-active PAHs in sediments contaminated by the Hebei Spirit oil spill: Application of Tenax extraction in effect-directed analysis.

    Science.gov (United States)

    Hong, Seongjin; Yim, Un Hyuk; Ha, Sung Yong; Shim, Won Joon; Jeon, Seungyeon; Lee, Sangwoo; Kim, Cheolmin; Choi, Kyungho; Jung, Jinho; Giesy, John P; Khim, Jong Seong

    2016-02-01

    Bioaccessibility of toxic substances in sedimentary residual oil is a crucial factor that needs to be considered for accurate risk assessments posed by oil spills. However, information on oil weathering processes and bioaccessibility of residual oil is often not sufficient and clear. In the present study, bioaccessibility of aryl hydrocarbon receptor (AhR)-active polycyclic aromatic hydrocarbons (PAHs) in coastal sediments near the site of the Hebei Spirit oil spill (Korea, 2007) was assessed by Tenax extraction in effect-directed analysis (EDA). Sediment samples collected 6 years after the oil spill were extracted using Soxhlet or Tenax, and EDA was performed using a battery of H4IIE-luc bioassay and GC/MSD analysis. Concentrations of PAHs and alkyl-PAHs in Soxhlet extracts ranged from 210 to 53,000 μg kg(-1) dry mass. However, concentrations of PAHs and alkyl-PAHs in Tenax extracts were approximately 20-fold less compared to those in Soxhlet extracts. In Soxhlet and Tenax extracts, the major AhR-active PAHs were identified as C1-chrysene, C3-chrysene, and C4-phenanthrene. Concentrations of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) equivalents (TEQ(PAHs)) explained 31% and 60% of the bioassay-derived TCDD-EQ concentrations in Soxhlet and Tenax extracts, respectively. Overall, bioaccessibility of PAHs and alkyl-PAHs in sedimentary residual oils depended on hydrophobicity (log K(ow)) and degree of weathering of crude oil. The results of the present study provide further evidence in support of the biological and ecological recoveries of oil spill sites. PMID:26408977

  7. A detailed kinetic modeling study of toluene oxidation in a premixed laminar flame

    Energy Technology Data Exchange (ETDEWEB)

    Tian, Z; Pitz, W J; Fournet, R; Glaude, P; Battin-Leclerc, F

    2009-12-18

    An improved chemical kinetic model for the toluene oxidation based on experimental data obtained in a premixed laminar low-pressure flame with vacuum ultraviolet (VUV) photoionization and molecular beam mass spectrometry (MBMS) techniques has been proposed. The present mechanism consists of 273 species up to chrysene and 1740 reactions. The rate constants of reactions of toluene, decomposition, reaction with oxygen, ipso-additions and metatheses with abstraction of phenylic H-atom are updated; new pathways of C{sub 4} + C{sub 2} species giving benzene and fulvene are added. Based on the experimental observations, combustion intermediates such as fulvenallene, naphtol, methylnaphthalene, acenaphthylene, 2-ethynylnaphthalene, phenanthrene, anthracene, 1-methylphenanthrene, pyrene and chrysene are involved in the present mechanism. The final toluene model leads to an overall satisfactory agreement between the experimentally observed and predicted mole fraction profiles for the major products and most combustion intermediates. The toluene depletion is governed by metathese giving benzyl radicals, ipso-addition forming benzene and metatheses leading to C{sub 6}H{sub 4}CH{sub 3} radicals. A sensitivity analysis indicates that the unimolecular decomposition via the cleavage of a C-H bond has a strong inhibiting effect, while decomposition via C-C bond breaking, ipso-addition of H-atom to toluene, decomposition of benzyl radicals and reactions related to C{sub 6}H{sub 4}CH{sub 3} radicals have promoting effect for the consumption of toluene. Moreover, flow rate analysis is performed to illustrate the formation pathways of mono- and polycyclic aromatics.

  8. Polycyclic aromatic hydrocarbons in milk powders marketed in Argentina and Brazil.

    Science.gov (United States)

    Garcia Londoño, Victor A; Garcia, Laura P; Scussel, Vildes M; Resnik, Silvia

    2013-01-01

    The aim of this study was to quantify polycyclic aromatic hydrocarbon (PAH) levels in milk powder samples commercialised in Argentina and Brazil during 2012. Thirty-one samples were available from the retail market. An HPLC method for the determination of PAHs was applied involving a clean-up step with silica cartridges. Recoveries were greater than 79% for all PAHs analysed. Reproducible determination with adequate detection and quantification limits (LOD and LOQ) were attained by HPLC with fluorescence detection for 14 PAHs. Acenaphthylene was determined with a UV-VIS detector. There is no significant difference in any PAHs or in the sum of them between the Argentinean and Brazilian samples. Therefore, the samples were evaluated together. The highest concentration of benzo(a)pyrene (BaP) detected was 0.57 µg kg⁻¹ in milk powder. Contamination of samples expressed as the sum of 15 analysed PAHs varied between 11.8 and 78.4 µg kg⁻¹ and as PAH4 (BaP, chrysene, benzo(a)anthracene and benzo(b)fluoranthene) was between 0.02 and 10.16 µg kg⁻¹. The correlation coefficient for PAH2 (BaP and chrysene) and PAH4 groups was 0.95, for PAH2 and PAH8 it was 0.71, and for PAH4 and PAH8 it was 0.83. All the samples were below the regulatory limit for BaP, but 65% of commercial milk powders do not comply with the European Union limit for PAH4. This is the first report of PAH contamination in powder milk from Argentina and Brazil.

  9. Hard Cap Espresso Machines in Analytical Chemistry: What Else?

    Science.gov (United States)

    Armenta, Sergio; de la Guardia, Miguel; Esteve-Turrillas, Francesc A

    2016-06-21

    A hard cap espresso machine has been used in combination with liquid chromatography with molecular fluorescence detection for the determination of polycyclic aromatic hydrocarbons (PAHs) from contaminated soils and sediments providing appropriate extraction efficiencies and quantitative results. Naphthalene, acenaphthene, fluorene, phenanthrene, anthracene, fluoranthene, pyrene, benz[a]anthracene, chrysene, benz[b]fluoranthene, benz[k]fluoranthene, benz[a]pyrene, dibenz[a,h]anthracene, benz[ghi]perylene, and indeno[1,2,3-cd]pyrene were used as target compounds. It should be mentioned that the pairs benz[a]anthracene-chrysene and dibenz[a,h]anthracene-benz[ghi]perylene peaks coelute under the employed chromatographic conditions; thus, those compounds were determined together. PAHs were extracted from 5.0 g of soil, previously homogenized, freeze-dried, and sieved to 250 μm, with 50 mL of 40% (v/v) acetonitrile in water at a temperature of 72 ± 3 °C. The proposed procedure is really fast, with an extraction time of 11 s, and it reduces the required amount of organic solvent to do the sample preparation. The obtained limit of detection for the evaluated PAHs was from 1 to 38 μg kg(-1). Recoveries were calculated using clean soils spiked with 100, 500, 1000, and 2000 μg kg(-1) PAHs with values ranging from 81 to 121% and good precision with relative standard deviation values lower than 30%. The method was validated using soil and sediment certified reference materials and also using real samples by comparison with ultrasound-assisted extraction, as reference methodology, obtaining statistically comparable results. Thus, the use of hard cap espresso machines in the analytical laboratories offers tremendous possibilities as low cost extraction units for the extraction of solid samples.

  10. The prestige oil spill. I. Biodegradation of a heavy fuel oil under simulated conditions.

    Science.gov (United States)

    Díez, Sergi; Sabatté, Jordi; Viñas, Marc; Bayona, Josep M; Solanas, Anna M; Albaigés, Joan

    2005-09-01

    In vitro biodegradation of the Prestige heavy fuel oil has been carried out using two microbial consortia obtained by enrichment in different substrates to simulate its environmental fate and potential utility for bioremediation. Different conditions, such as incubation time (i.e., 20 or 40 d), oil weathering, and addition of an oleophilic fertilizer (S200), were evaluated. Weathering slowed down the degradation of the fuel oil, probably because of the loss of lower and more labile components, but the addition of S200 enhanced significantly the extension of the biodegradation. n-Alkanes, alkylcyclohexanes, alkylbenzenes, and the two- to three-ring polycyclic aromatic hydrocarbons (PAHs) were degraded in 20 or 40 d of incubation of the original oil, whereas the biodegradation efficiency decreased for higher PAHs and with the increase of alkylation. Molecular markers were degraded according to the following sequence: Acyclic isoprenoids > diasteranes > C27-steranes > betabeta-steranes > homohopanes > monoaromatic steranes > triaromatic steranes. Isomeric selectivity was observed within the C1- and C2-phenanthrenes, dibenzothiophenes, pyrenes, and chrysenes, providing source and weathering indices for the characterization of the heavy oil spill. Acyclic isoprenoids, C27-steranes, C1- and C2-naphthalenes, phenanthrenes, and dibenzothiophenes were degraded completely when S200 was used. The ratios of the C2- and C3-alkyl homologues of fluoranthene/pyrene and chrysene/benzo[a]anthracene are proposed as source ratios in moderately degraded oils. The 4-methylpyrene and 3-methylchrysene were refractory enough to serve as conserved internal markers in assessing the degradation of the aromatic fraction in a manner similar to that of hopane, as used for the aliphatic fraction.

  11. Effect-directed analysis and mixture effects of AhR-active PAHs in crude oil and coastal sediments contaminated by the Hebei Spirit oil spill

    International Nuclear Information System (INIS)

    The major AhR-active PAHs were identified in crude oil and oil-contaminated sediments by use of effect-directed analysis. As part of the study, an enhanced potency balance analysis was conducted by establishing the novel relative potency values of (alkyl)-PAHs from the H4IIE-luc bioassay. Silica gel column fractionation of crude oil resulted in greater AhR-mediated potencies in fractions of aromatics (F2) and resins (F3), and such trend was also observed for field collected sediment samples. AhR-mediated potencies of six F2 sub-fractions from HPLC indicated that the majority of F2 responses were attributable to 3–4 ring aromatics. Target PAHs including C4-phenanthrene, C1-chrysene, and C3-chrysene in sediments explained ∼18% of the bioassay-derived TCDD-EQs, however, the unknown AhR agonists and potential mixture effects remain in question. Overall, the AhR-potency and antagonistic potential of residual oil in sediment tended to decrease over time, thus monitoring of weathering process would be key for the post management of oil-contaminated sites. - Highlights: • AhR-active PAHs in crude oil and sediments were newly determined using EDA. • Novel relative potency values of (alkyl)-PAHs for AhR activity were established. • Three to four ring PAHs were identified to be major AhR agonists in crude oil. • Parent and alkyl-PAHs explained ∼18% of the total AhR-mediated potencies of crude oil. • AhR-mediated potencies apparently decreased by the timely weathering processes. - “Major AhR agonists were identified three to four ring PAHs in crude oil and sediments determined by use of effect-directed analysis.”

  12. Effect of recurrent sediment resuspension-deposition events on bioavailability of polycyclic aromatic hydrocarbons in aquatic environments

    Science.gov (United States)

    Dong, Jianwei; Xia, Xinghui; Wang, Minghu; Xie, Hui; Wen, Jiaojiao; Bao, Yimeng

    2016-09-01

    To investigate the effect of recurrent sediment resuspension-deposition events (RSRDEs) on bioavailability of polycyclic aromatic hydrocarbons (PAHs) in aquatic environments, a modified device was used to simulate three resuspension-deposition events with the sediment collected from the Yellow River. The results showed that the dissolved organic carbon (DOC)-water distribution coefficients of PAHs decreased with time during the first resuspension-deposition period. It indicates that some PAHs associated with organic carbon (OC) in suspended sediment (SPS) desorbed with the release of OC and became DOC-associated PAHs in the overlying water, then the PAHs desorbed from the DOC and became freely dissolved. After first 2-h suspension, only 1.90% of phenanthrene, 2.98% of pyrene, and 0.33% of chrysene in the overlying water came from pore-water; at least 61.6%, 89.6%, and 95.3% came from DOC-associated PAHs in SPS and the rests were released from the insoluble OC in SPS. The maximum desorption ratios in the original sediment were 20%, 12%, and 14% for phenanthrene, pyrene, and chrysene, respectively during the first resuspension-deposition event. The SPS concentration followed the sequence of the third > second > first resuspension event. This was because RSRDEs changed the SPS particle size and enhanced floc formation. There was no significant difference in the total dissolved PAH concentrations among the three resuspension events, while their freely dissolved concentrations followed the sequence of the third > second > first resuspension event. During deposition periods, more than half of the total/freely dissolved PAHs released during suspension still existed in the overlying water after 70-h deposition. This study suggests that the RSRDEs will increase the bioavailability of PAHs in aquatic environments, especially near the sediment-water interface, and the potential effects of PAHs during RSRDEs on fish/human in rivers and lakes should be considered in future

  13. WATER AS A REAGENT FOR SOIL REMEDIATION

    Energy Technology Data Exchange (ETDEWEB)

    Indira S. Jayaweera; Montserrat Marti-Perez; Jordi Diaz-Ferrero; Angel Sanjurjo

    2001-03-29

    SRI International is conducting experiments to develop and evaluate hydrothermal extraction technology or hot water extraction (HWE) technology for remediating petroleum-contaminated soils. Most current remediation practices either fail to remove the polycyclic aromatic hydrocarbons (PAHs) found in petroleum-contaminated sites, are too costly, or require the use of organic solvents at the expense of additional contamination and with the added cost of recycling solvents. Hydrothermal extraction offers the promise of efficiently extracting PAHs and other kinds of organics from contaminated soils at moderate temperatures and pressures, using only water and inorganic salts such as carbonate. SRI has conducted experiments to measure the solubility and rate of solubilization of selected PAHs (fluoranthene, pyrene, chrysene, 9,10-dimethylanthracene) in water using SRI's hydrothermal optical cell with the addition of varying amounts of sodium carbonate to evaluate the efficiency of the technology for removing PAHs from the soil. SRI data shows a very rapid increase in solubility of PAHs with increase in temperature in the range 25-275 C. SRI also measured the rate of solubilization, which is a key factor in determining the reactor parameters. SRI results for fluoranthene, pyrene, chrysene, and 9,10-dimethylanthracene show a linear relationship between rate of solubilization and equilibrium solubility. Also, we have found the rate of solubilization of pyrene at 275 C to be 6.5 ppm/s, indicating that the equilibrium solubilization will be reached in less than 3 min at 275 C; equilibrium solubility of pyrene at 275 C is 1000 ppm. Also, pyrene and fluoranthene appear to have higher solubilities in the presence of sodium carbonate. In addition to this study, SRI studied the rate of removal of selected PAHs from spiked samples under varying conditions (temperature, pore sizes, and pH). We have found a higher removal of PAHs in the presence of sodium carbonate in both sand

  14. Cytochrome P450 1b1 in polycyclic aromatic hydrocarbon (PAH)-induced skin carcinogenesis: Tumorigenicity of individual PAHs and coal-tar extract, DNA adduction and expression of select genes in the Cyp1b1 knockout mouse

    Energy Technology Data Exchange (ETDEWEB)

    Siddens, Lisbeth K. [Department of Environmental and Molecular Toxicology, Oregon State University, Corvallis, OR 97331 (United States); Superfund Research Center, Oregon State University, Corvallis, OR 97331 (United States); Bunde, Kristi L. [College of Veterinary Medicine, Oregon State University, Corvallis, OR 97331 (United States); Harper, Tod A. [Department of Environmental and Molecular Toxicology, Oregon State University, Corvallis, OR 97331 (United States); Linus Pauling Institute, Oregon State University, Corvallis, OR 97331 (United States); Environmental Health Sciences Center, Oregon State University, Corvallis, OR 97331 (United States); McQuistan, Tammie J. [Superfund Research Center, Oregon State University, Corvallis, OR 97331 (United States); Linus Pauling Institute, Oregon State University, Corvallis, OR 97331 (United States); Löhr, Christiane V. [Environmental Health Sciences Center, Oregon State University, Corvallis, OR 97331 (United States); College of Veterinary Medicine, Oregon State University, Corvallis, OR 97331 (United States); Bramer, Lisa M. [Applied Statistics and Computational Modeling, Pacific Northwest National Laboratory, Richland, WA 99352 (United States); Waters, Katrina M. [Superfund Research Center, Oregon State University, Corvallis, OR 97331 (United States); Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA 99352 (United States); Tilton, Susan C. [Department of Environmental and Molecular Toxicology, Oregon State University, Corvallis, OR 97331 (United States); Superfund Research Center, Oregon State University, Corvallis, OR 97331 (United States); Krueger, Sharon K. [Department of Environmental and Molecular Toxicology, Oregon State University, Corvallis, OR 97331 (United States); Superfund Research Center, Oregon State University, Corvallis, OR 97331 (United States); Linus Pauling Institute, Oregon State University, Corvallis, OR 97331 (United States); and others

    2015-09-01

    FVB/N mice wild-type, heterozygous or null for Cyp 1b1 were used in a two-stage skin tumor study comparing PAH, benzo[a]pyrene (BaP), dibenzo[def,p]chrysene (DBC), and coal tar extract (CTE, SRM 1597a). Following 20 weeks of promotion with TPA the Cyp 1b1 null mice, initiated with DBC, exhibited reductions in incidence, multiplicity, and progression. None of these effects were observed with BaP or CTE. The mechanism of Cyp 1b1-dependent alteration of DBC skin carcinogenesis was further investigated by determining expression of select genes in skin from DBC-treated mice 2, 4 and 8 h post-initiation. A significant reduction in levels of Cyp 1a1, Nqo1 at 8 h and Akr 1c14 mRNA was observed in Cyp 1b1 null (but not wt or het) mice, whereas no impact was observed in Gst a1, Nqo 1 at 2 and 4 h or Akr 1c19 at any time point. Cyp 1b1 mRNA was not elevated by DBC. The major covalent DNA adducts, dibenzo[def,p]chrysene-(±)-11,12-dihydrodiol-cis and trans-13,14-epoxide-deoxyadenosine (DBCDE-dA) were quantified by UHPLC-MS/MS 8 h post-initiation. Loss of Cyp1 b1 expression reduced DBCDE-dA adducts in the skin but not to a statistically significant degree. The ratio of cis- to trans-DBCDE-dA adducts was higher in the skin than other target tissues such as the spleen, lung and liver (oral dosing). These results document that Cyp 1b1 plays a significant role in bioactivation and carcinogenesis of DBC in a two-stage mouse skin tumor model and that loss of Cyp 1b1 has little impact on tumor response with BaP or CTE as initiators. - Highlights: • Cyp1b1 null mice exhibit lower skin cancer sensitivity to DBC but not BaP or CTE. • Cyp1b1 expression impacts expression of other PAH metabolizing enzymes. • cis/trans-DBCDE-dA ratio significantly higher in the skin than the spleen, lung or liver • Potency of DBC and CTE in mouse skin is higher than predicted by RPFs.

  15. Effects of crude oil exposure on bioaccumulation of polycyclic aromatic hydrocarbons and survival of adult and larval stages of gelatinous zooplankton.

    Directory of Open Access Journals (Sweden)

    Rodrigo Almeda

    Full Text Available Gelatinous zooplankton play an important role in marine food webs both as major consumers of metazooplankton and as prey of apex predators (e.g., tuna, sunfish, sea turtles. However, little is known about the effects of crude oil spills on these important components of planktonic communities. We determined the effects of Louisiana light sweet crude oil exposure on survival and bioaccumulation of polycyclic aromatic hydrocarbons (PAHs in adult stages of the scyphozoans Pelagia noctiluca and Aurelia aurita and the ctenophore Mnemiopsis leidyi, and on survival of ephyra larvae of A. aurita and cydippid larvae of M. leidyi, in the laboratory. Adult P. noctiluca showed 100% mortality at oil concentration ≥20 µL L(-1 after 16 h. In contrast, low or non-lethal effects were observed on adult stages of A. aurita and M. leidyi exposed at oil concentration ≤25 µL L(-1 after 6 days. Survival of ephyra and cydippid larva decreased with increasing crude oil concentration and exposition time. The median lethal concentration (LC50 for ephyra larvae ranged from 14.41 to 0.15 µL L(-1 after 1 and 3 days, respectively. LC50 for cydippid larvae ranged from 14.52 to 8.94 µL L(-1 after 3 and 6 days, respectively. We observed selective bioaccumulation of chrysene, phenanthrene and pyrene in A. aurita and chrysene, pyrene, benzo[a]pyrene, benzo[b]fluoranthene, benzo[k]fluoranthene, and benzo[a]anthracene in M. leidyi. Overall, our results indicate that (1 A. aurita and M. leidyi adults had a high tolerance to crude oil exposure compared to other zooplankton, whereas P. noctiluca was highly sensitive to crude oil, (2 larval stages of gelatinous zooplankton were more sensitive to crude oil than adult stages, and (3 some of the most toxic PAHs of crude oil can be bioaccumulated in gelatinous zooplankton and potentially be transferred up the food web and contaminate apex predators.

  16. Profile distribution of polycyclic aromatic hydrocarbons in soils of drained peatlands after wildfires (Moscow region, Russia)

    Science.gov (United States)

    Tsibart, Anna; Gennadiev, Alexander; Koshovskii, Timur; Kovach, Roman

    2014-05-01

    Polycyclic aromatic compounds (PAHs) are formed in different natural and anthropogenic processes and could be found in many landscape components. These compounds are carcinogenic and belong to the group of persistent organic pollutants. The anthropogenic sources of PAHs are well-studied, but insufficient data are available on the hightemperature production of PAHs in natural processes. For example, natural fires are frequently related to the PAHs sources in landscapes, but very little factual data are on this topic. The soils of drained peatlands affected by catastrophic wildfires of 2010 and 2002 were studied in the Eastern part of Moscow Region (Russia). A total of 14 profiles of histosols and histic podsols were investigated. These series included soils of plots subjected to fires of different intensities and age, as well as soils of the background plots. Soil samples were taken from genetic horizons and from every 10 cm. The samples were analyzed for the contents of 14 prevailing individual compounds: fluorene, naphthalene, phenanthrene, chrysene, pyrene, anthracene, tetraphene, benz[a]pyrene, benzo[ghi]perylene, benzo[e]pyrene, coronene, dibenztiophene, triphenilene, benz(k)fluorantene. Morfological properties of soils after wildfires on drained peatlands were changed dramatically, the horizons of ash and char instead of organic layers were formed. These new horizons differ in the capability of PAHs accumulation. The char horizons have the highest concentrations of PAHs - up to 300 ng/g because of incomplete burning of organic matter in this sites, and the ash horizons, where the complete burning occured, contain only 10 ng/g PAHs. The highest concentrations of PAHs in soil profiles were detected after recent fires, and in cases of thick peat layers. After the combustion of peat chrysene, benz[a]pyrene, benz[e]pyrene, benzo[ghi]perylene, benz(k)fluorantene and tetraphene accumulated in soils. This is mainly the group of 4-6-nuclear compounds. The formation of

  17. Assessment of Fish Habitat, Water Quality, and Selected Contaminants in Streambed Sediments in Noyes Slough, Fairbanks, Alaska, 2001-2002

    Science.gov (United States)

    Kennedy, Ben W.; Whitman, Matthew S.; Burrows, Robert L.; Richmond, Sharon A.

    2004-01-01

    During 2001-2002, the U.S. Geological Survey sampled streambed sediment at 23 sites, measured water quality at 26 sites, and assessed fish habitat for the entire length of Noyes Slough, a 5.5-mile slough of the Chena River in Fairbanks, Alaska. These studies were undertaken to document the environmental condition of the slough and to provide information to the public for consideration in plans to improve environmental conditions of the waterway. The availability of physical habitat for fish in the slough does not appear to be limited, although some beaver dams and shallow water may restrict movement, particularly during low flow. Elevated water temperatures in summer and low dissolved-oxygen concentrations are the principle factors adversely affecting water quality in Noyes Slough. Increased flow mitigated poor water-quality conditions and reduced the number of possible fish barriers. Flow appears to be the most prominent mechanism shaping water quality and fish habitat in Noyes Slough. Streambed sediment samples collected at 23 sites in 2001 were analyzed for 24 trace elements. Arsenic, lead, and zinc were the only trace elements detected in concentrations that exceed probable effect levels for the protection of aquatic life. The background concentration for arsenic in Noyes Slough is naturally elevated because of significant concentrations of arsenic in local bedrock and ground water. Sources of the zinc and lead contamination are uncertain, however both lead and zinc are common urban contaminants. Streambed-sediment samples from 12 sites in 2002 were analyzed for organochlorine pesticides, polychlorinated biphenyls (PCBs), and semivolatile organic compounds (SVOCs). The concentration of bis(2-ethylhexyl)phthalate of 2,600 micrograms per kilogram (?g/kg) for one sample from the site above Aurora Drive approached the aquatic-life criterion of 2,650 ?g/kg. Low concentrations of p-cresol, chrysene, and fluoranthene were detected in most of the sediment samples. The

  18. Cytochrome P450 1b1 in polycyclic aromatic hydrocarbon (PAH)-induced skin carcinogenesis: Tumorigenicity of individual PAHs and coal-tar extract, DNA adduction and expression of select genes in the Cyp1b1 knockout mouse.

    Science.gov (United States)

    Siddens, Lisbeth K; Bunde, Kristi L; Harper, Tod A; McQuistan, Tammie J; Löhr, Christiane V; Bramer, Lisa M; Waters, Katrina M; Tilton, Susan C; Krueger, Sharon K; Williams, David E; Baird, William M

    2015-09-01

    FVB/N mice wild-type, heterozygous or null for Cyp 1b1 were used in a two-stage skin tumor study comparing PAH, benzo[a]pyrene (BaP), dibenzo[def,p]chrysene (DBC), and coal tar extract (CTE, SRM 1597a). Following 20 weeks of promotion with TPA the Cyp 1b1 null mice, initiated with DBC, exhibited reductions in incidence, multiplicity, and progression. None of these effects were observed with BaP or CTE. The mechanism of Cyp 1b1-dependent alteration of DBC skin carcinogenesis was further investigated by determining expression of select genes in skin from DBC-treated mice 2, 4 and 8h post-initiation. A significant reduction in levels of Cyp 1a1, Nqo1 at 8h and Akr 1c14 mRNA was observed in Cyp 1b1 null (but not wt or het) mice, whereas no impact was observed in Gst a1, Nqo 1 at 2 and 4h or Akr 1c19 at any time point. Cyp 1b1 mRNA was not elevated by DBC. The major covalent DNA adducts, dibenzo[def,p]chrysene-(±)-11,12-dihydrodiol-cis and trans-13,14-epoxide-deoxyadenosine (DBCDE-dA) were quantified by UHPLC-MS/MS 8h post-initiation. Loss of Cyp1 b1 expression reduced DBCDE-dA adducts in the skin but not to a statistically significant degree. The ratio of cis- to trans-DBCDE-dA adducts was higher in the skin than other target tissues such as the spleen, lung and liver (oral dosing). These results document that Cyp 1b1 plays a significant role in bioactivation and carcinogenesis of DBC in a two-stage mouse skin tumor model and that loss of Cyp 1b1 has little impact on tumor response with BaP or CTE as initiators. PMID:26049101

  19. Public health assessment for Ralph Gray Trucking Company (A/K/A Westminster Tract No. 2633), Westminster, Orange County, California, region 9. CERCLIS No. CAD981995947. Preliminary report

    Energy Technology Data Exchange (ETDEWEB)

    1993-06-18

    The Ralph D. Gray Trucking site consists of 73 homes in west Orange County, California. Records suggest that oil refinery wastes were originally deposited there in the 1930s and then were redeposited in three locations during housing development in the late 1950s. The buried oil refinery waste are located in the backyards of approximately 29 residences. Seeps of tar-like material have surfaced in some of the yards. Chemical analysis of the waste material has shown that it contains volatile aromatic hydrocarbons like benzene, ethylbenzene, toluene, and xylenes; polyclic aromatic hydrocarbons like benzo(a)pyrene, phenanthrene, and chrysene; thiophene derivatives, which include smelly, sulfur-containing compounds; some trace metals like arsenic and chromium; and high levels of sulfate. The preliminary public health assessment identifies two potential exposure pathways of health concern at the Ralph D. Gray Trucking site. Residents may be exposed to waste contaminants from eating vegetables or fruits grown in their yards. The most likely contaminants to assimilate into vegetation are the polycyclic aromatic hydrocarbons, chromium, arsenic, and lead, but no actual chemical analyses have been conducted of any fruits and vegetables. Site residents, especially children, may incidentally/accidentally ingest or have skin contact with the waste material or with contaminated surface soil and thus be exposed to a number of contaminants.

  20. Temperature-mediated polymorphism in molecular crystals: The impact on crystal packing and charge transport

    KAUST Repository

    Stevens, Loah A.

    2015-01-13

    We report a novel synthesis to ultra high purity 7,14-bis((trimethylsilyl)ethynyl)dibenzo[b,def]-chrysene (TMS-DBC) and the use of this material in the growth of single crystals by solution and vapor deposition techniques. We observe that the substrate temperature has a dramatic impact on the crystal growth, producing two distinct polymorphs of TMS-DBC; low temperature (LT) fine red needles and high temperature (HT) large yellow platelets. Single crystal X-ray crystallography confirms packing structures where the LT crystals form a 1D slipped-stack structure, while the HT crystals adopt a 2D brickwork motif. These polymorphs also represent a rare example where both are extremely stable and do not interconvert to the other crystal structure upon solvent or thermal annealing. Single crystal organic field-effect transistors of the LT and HT crystals show that the HT 2D brickwork motif produces hole mobilities as high as 2.1 cm2 V-1 s-1, while the mobility of the 1D structure is significantly lower, at 0.028 cm2 V-1 s-1. Electronic-structure calculations indicate that the superior charge transport in the brickwork polymorph in comparison to the slipped-stack polymorph is due to the presence of an increased dimensionality of the charge migration pathways.

  1. Organic compounds downstream from a treated-wastewater discharge near Dallas, Texas, March 1987

    Science.gov (United States)

    Buszka, P.M.; Barber, L.B., II; Schroeder, M.P.; Becker, L.D.

    1994-01-01

    Water and streambed-sediment samples were collected on March 9 and 10,1987 from one site upstream and three sites downstream of the discharge from a municipal wastewater-treatment plant on Rowlett Creek near Dallas, Texas. To extract and separate organic compounds, purgeand-trap, closed-loop stripping, and pH-adjusted solvent extraction methods were used for water samples; and a Soxhlet-solvent extraction method was used for streambed sediment. These methods were combined with gas chromatography/mass spectrometry to identify organic compounds in Rowlett Creek. Results from this study confirm the persistence of many organic compounds in water as far as 13.5 kilometers downstream of the wastewater discharge. These include: (1) the volatile organic compounds chloroform, 1,2-dichlorobenzene, 1,4-dichlorobenzene, tetrachloroethene, and trichloroethene; (2) several linear alkylbenzene compounds, octyl phenol, and a tetramethylbutyl phenol isomer that are related to detergent use; (3) 9-phenyl-9H-carbazole, a compound related to coal tars and coal combustion residues; and (4) caffeine. The only compound present in water in concentrations greater than U.S. Environmental Protection Agency maximum contaminant levels for drinking water was tetrachloroethene (6.0 micrograms per liter) in a sample collected 13.5 kilometers downstream from the waste water discharge. Compounds identified from the streambed-sediment samples include a xylene isomer at 7.7 kilometers downstream and chrysene, fluoranthene, pyrene, and a xylene isomer at 13.5 kilometers downstream from the wastewater discharge.

  2. Concentrations of Contaminants with Regulatory Limits in Samples of Clam (Chamelea gallina) Collected along the Abruzzi Region Coast in Central Italy.

    Science.gov (United States)

    Visciano, Pierina; Scortichini, Giampiero; Suzzi, Giovanna; Diletti, Gianfranco; Schirone, Maria; Martino, Giuseppe

    2015-09-01

    Concentrations of pollutants with regulatory limits were determined in specimens of Chamelea gallina, a species of clam collected along the Abruzzi coastal region of the central Adriatic Sea. Nine sampling sites were selected to evaluate the distribution of contaminants in the environment and the health risk for consumers. The concentrations of all the examined compounds were lower than the maximums set by European legislation. Polycyclic aromatic hydrocarbons and total mercury were below the detection limit (0.18 μg/kg for benzo[a]anthracene, 0.30 μg/kg for chrysene, 0.12 μg/kg for benzo[b]fluoranthene, 0.08 μg/kg for benzo[a]pyrene, and 0.0050 mg/kg for total mercury) in all the analyzed samples. Mean concentrations of lead and cadmium were 0.104 and 0.110 mg/kg, respectively. Of the non-dioxin-like polychlorinated biphenyls, PCB-153, PCB-180, and PCB-138 were the most abundant at all sampling sites (1a to 9a) at 0.25 mi (ca. 0.4 km) and at some sampling sites (1b, 2b, 3b, 5b and 7b) at 0.35 mi (ca. 0.56 km). Principal component analysis revealed that the concentrations of dioxin-like polychlorinated biphenyls were similar at the majority of sampling sites, and O8CDD and 2,3,7,8-T4CDF were the predominant dioxin congeners.

  3. Sample preparation of sewage sludge and soil samples for the determination of polycyclic aromatic hydrocarbons based on one-pot microwave-assisted saponification and extraction.

    Science.gov (United States)

    Pena, M Teresa; Pensado, Luis; Casais, M Carmen; Mejuto, M Carmen; Cela, Rafael

    2007-04-01

    A microwave-assisted sample preparation (MASP) procedure was developed for the analysis of polycyclic aromatic hydrocarbons (PAHs) in sewage sludge and soil samples. The procedure involved the simultaneous microwave-assisted extraction of PAHs with n-hexane and the hydrolysis of samples with methanolic potassium hydroxide. Because of the complex nature of the samples, the extracts were submitted to further cleaning with silica and Florisil solid-phase extraction cartridges connected in series. Naphthalene, acenaphthene, fluorene, phenanthrene, anthracene, fluoranthene, pyrene, benz[a]anthracene, chrysene, benzo[e]pyrene, benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[a]pyrene, dibenz[a,h]anthracene, benzo[g,h,i]perylene, and indeno[1,2,3-cd]pyrene, were considered in the study. Quantification limits obtained for all of these compounds (between 0.4 and 14.8 microg kg(-1) dry mass) were well below of the limits recommended in the USA and EU. Overall recovery values ranged from 60 to 100%, with most losses being due to evaporation in the solvent exchange stages of the procedure, although excellent extraction recoveries were obtained. Validation of the accuracy was carried out with BCR-088 (sewage sludge) and BCR-524 (contaminated industrial soil) reference materials. PMID:17268774

  4. 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.

  5. Sample preparation of sewage sludge and soil samples for the determination of polycyclic aromatic hydrocarbons based on one-pot microwave-assisted saponification and extraction

    Energy Technology Data Exchange (ETDEWEB)

    Pena, M.T.; Pensado, Luis; Casais, M.C.; Mejuto, M.C.; Cela, Rafael [Universidad de Santiago de Compostela, Dpto. Quimica Analitica, Nutricion y Bromatologia. Instituto de Investigacion y Analisis Alimentario, Santiago de Compostela (Spain)

    2007-04-15

    A microwave-assisted sample preparation (MASP) procedure was developed for the analysis of polycyclic aromatic hydrocarbons (PAHs) in sewage sludge and soil samples. The procedure involved the simultaneous microwave-assisted extraction of PAHs with n-hexane and the hydrolysis of samples with methanolic potassium hydroxide. Because of the complex nature of the samples, the extracts were submitted to further cleaning with silica and Florisil solid-phase extraction cartridges connected in series. Naphthalene, acenaphthene, fluorene, phenanthrene, anthracene, fluoranthene, pyrene, benz[a]anthracene, chrysene, benzo[e]pyrene, benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[a]pyrene, dibenz[a,h]anthracene, benzo[g,h,i]perylene, and indeno[1,2,3-cd]pyrene, were considered in the study. Quantification limits obtained for all of these compounds (between 0.4 and 14.8 {mu}g kg{sup -1} dry mass) were well below of the limits recommended in the USA and EU. Overall recovery values ranged from 60 to 100%, with most losses being due to evaporation in the solvent exchange stages of the procedure, although excellent extraction recoveries were obtained. Validation of the accuracy was carried out with BCR-088 (sewage sludge) and BCR-524 (contaminated industrial soil) reference materials. (orig.)

  6. Concentration dependence of biotransformation in fish liver S9: Optimizing substrate concentrations to estimate hepatic clearance for bioaccumulation assessment.

    Science.gov (United States)

    Lo, Justin C; Allard, Gayatri N; Otton, S Victoria; Campbell, David A; Gobas, Frank A P C

    2015-12-01

    In vitro bioassays to estimate biotransformation rate constants of contaminants in fish are currently being investigated to improve bioaccumulation assessments of hydrophobic contaminants. The present study investigates the relationship between chemical substrate concentration and in vitro biotransformation rate of 4 environmental contaminants (9-methylanthracene, pyrene, chrysene, and benzo[a]pyrene) in rainbow trout (Oncorhynchus mykiss) liver S9 fractions and methods to determine maximum first-order biotransformation rate constants. Substrate depletion experiments using a series of initial substrate concentrations showed that in vitro biotransformation rates exhibit strong concentration dependence, consistent with a Michaelis-Menten kinetic model. The results indicate that depletion rate constants measured at initial substrate concentrations of 1 μM (a current convention) could underestimate the in vitro biotransformation potential and may cause bioconcentration factors to be overestimated if in vitro biotransformation rates are used to assess bioconcentration factors in fish. Depletion rate constants measured using thin-film sorbent dosing experiments were not statistically different from the maximum depletion rate constants derived using a series of solvent delivery-based depletion experiments for 3 of the 4 test chemicals. Multiple solvent delivery-based depletion experiments at a range of initial concentrations are recommended for determining the concentration dependence of in vitro biotransformation rates in fish liver fractions, whereas a single sorbent phase dosing experiment may be able to provide reasonable approximations of maximum depletion rates of very hydrophobic substances. PMID:26077187

  7. Carcinogenic polycyclic aromatic hydrocarbons in umbilical cord blood of human neonates from Guiyu, China

    Energy Technology Data Exchange (ETDEWEB)

    Guo, Yongyong; Huo, Xia [Analytic Cytology Laboratory and the Key Immunopathology Laboratory of Guangdong Province, Shantou University Medical College, Shantou (China); Wu, Kusheng [Analytic Cytology Laboratory and the Key Immunopathology Laboratory of Guangdong Province, Shantou University Medical College, Shantou (China); Department of Preventive Medicine, Shantou University Medical College, Shantou (China); Liu, Junxiao; Zhang, Yuling [Analytic Cytology Laboratory and the Key Immunopathology Laboratory of Guangdong Province, Shantou University Medical College, Shantou (China); Xu, Xijin, E-mail: xuxj@stu.edu.cn [Analytic Cytology Laboratory and the Key Immunopathology Laboratory of Guangdong Province, Shantou University Medical College, Shantou (China); Department of Cell Biology and Genetics, Shantou University Medical College, Shantou (China)

    2012-06-15

    Unregulated electronic-waste recycling results in serious environmental pollution of polycyclic aromatic hydrocarbons (PAHs) in Guiyu, China. We evaluated the body burden of seven carcinogenic PAHs and potential health risks for neonates. Umbilical cord blood (UCB) samples were collected from Guiyu (n = 103), and the control area of Chaonan (n = 80), China. PAHs in UCB were determined by gas chromatography/mass spectrometry. The median N-Ary-Summation 7c-PAH concentration was 108.05 ppb in UCB samples from Guiyu, vs. 79.36 ppb in samples from Chaonan. Residence in Guiyu and longer cooking time of food during the gestation period were significant factors contributing to the N-Ary-Summation 7c-PAH level. Benzo[a]anthracene (BaA), chrysene (Chr), and benzo[a]pyrene (BaP) were found to correlate with reduced neonatal height and gestational age. Infants experiencing adverse birth outcomes, on the whole, displayed higher BaA, Chr, and BaP levels compared to those with normal outcomes. We conclude that maternal PAH exposure results in fetal accumulation of toxic PAHs, and that such prenatal exposure correlates with adverse effects on neonatal health.

  8. PAH in Barbecued Meat from Restaurants and by Home-Grilling in Denmark

    DEFF Research Database (Denmark)

    Duedahl-Olesen, Lene; Meinert, L.; Aaslyng, M.;

    2011-01-01

    [a]pyrene (BaP), benzo[a]anthracene, benzo[b]fluoranthene and chrysene). PAHs were extracted by Pressurized Liquid Extraction followed by clean-up by GPC (Bio Beads, S-X3) and SPE (500mg, Silica) and finally analyzed by GC-MS. Home-grilled beef were found to contain highest concentrations of BaP (up to 24 µg....../kg) whereas commercially barbecued hamburgers were found to contain BaP up to 13.7 µg/kg. Chicken was found to contain the lowest BaP concentrations (0-0.1µg/kg). The highest concentration of BaP for chicken was 3.1 µg/kg detected in a commercially barbecued marinated chicken with skin. The sum of PAH 4...... ranged from below the detection limit to the highest concentration for a home-grilled beef (64 µg/kg). Worst case estimates revealed a margin of exposure (MOE) of approximately 18,000 for both BaP and the sum of PAH 4 for grilled meat only. The European Food Safety Authority (EFSA) has previously...

  9. Large-scale risk assessment of polycyclic aromatic hydrocarbons in shoreline sediments from Saudi Arabia: Environmental legacy after twelve years of the Gulf war oil spill

    Energy Technology Data Exchange (ETDEWEB)

    Bejarano, Adriana C., E-mail: ABejarano@researchplanning.co [Research Planning Inc., 1121 Park St., Columbia, SC 29201 (United States); Michel, Jacqueline [Research Planning Inc., 1121 Park St., Columbia, SC 29201 (United States)

    2010-05-15

    A large-scale assessment of polycyclic aromatic hydrocarbons (PAHs) from the 1991 Gulf War oil spill was performed for 2002-2003 sediment samples (n = 1679) collected from habitats along the shoreline of Saudi Arabia. Benthic sediment toxicity was characterized using the Equilibrium Partitioning Sediment Benchmark Toxic Unit approach for 43 PAHs (ESBTU{sub FCV,43}). Samples were assigned to risk categories according to ESBTU{sub FCV,43} values: no-risk (<=1), low (>1-<=2), low-medium (>2-<=3), medium (>3-<=5) and high-risk (>5). Sixty seven percent of samples had ESBTU{sub FCV,43} > 1 indicating potential adverse ecological effects. Sediments from the 0-30 cm layer from tidal flats, and the >30-<60 cm layer from heavily oiled halophytes and mangroves had high frequency of high-risk samples. No-risk samples were characterized by chrysene enrichment and depletion of lighter molecular weight PAHs, while high-risk samples showed little oil weathering and PAH patterns similar to 1993 samples. North of Safaniya sediments were not likely to pose adverse ecological effects contrary to sediments south of Tanaqib. Landscape and geomorphology has played a role on the distribution and persistence in sediments of oil from the Gulf War. - Risk Assessment of PAHs in shoreline sediments 12 years after the Gulf War oil spill.

  10. 人类胰腺癌组织中多环芳烃含量的测定及意义%The detection and significance of polycyclic aromatic hydrocarbons in human pancreatic cancer

    Institute of Scientific and Technical Information of China (English)

    Shuntao Liu; Limin Lun

    2012-01-01

    Objective: The aim of this study was to investigate the effect of polycyclic aromatic hydrocarbons (PAHs) on the occurrence of human pancreatic cancer.Methods: PAHs in human pancreatic cancer, adjacent pancreatic cancer tissues and tissues without pancreatic cancer were extracted by ultrasonic extraction (UE).And then the extracts were cleaned up by solid phase extraction and analyzed by high performance liquid chromatography (HPLC) with fluorescence spectroscopy.Results: Four kinds of PAHs were detected, which were chrysene, 2-methylanthracene, pyrene and benzo (a) pyrene.The contents of the four PAHs were not statistically significant between pancreatic cancer and adjacent tissues (P > 0.05).The contents of 2-methylanthracene, pyrene and benzo (a) pyrene in pancreatic cancer and adjacent tissues were higher than tissues without pancreatic cancer, the differences were statistically significant (P 0.05).Conclusion: PAHs were found in human pancreatic tissues.Human pancreatic tissues have extremely strong ability of bio-concentrating PAHs.PAHs might play an important role in the occurrence of human pancreatic cancer.

  11. Subtle effects of the water soluble fraction of oil spills on natural phytoplankton assemblages enclosed in mesocosms

    Science.gov (United States)

    González, J.; Fernández, E.; Figueiras, F. G.; Varela, M.

    2013-06-01

    Four mesocosm experiments were conducted to evaluate the effect of episodic oil spills on coastal marine phytoplankton assemblages. The experimental design was selected to simulate the Prestige oil spill, which occurred in Galician coastal waters (NW Iberia) in November 2002. The empirical results indicate that no significant direct effects of the water soluble fraction of oil (20-60 μg l-1 of chrysene equivalents) on phytoplankton biomass and production were observed immediately after oil additions. Despite this, subtle negative effects on primary production were detected using a modelling approach, being the impact lower on phytoplankton communities dominated by diatoms. Consistent with the reduced direct effect of oil additions on phytoplankton biomass and photosynthesis-related variables, no indirect trophic cascading effects, previously reported in microcosm experiments, were detected. This shows that the effect of punctual inputs of the water accommodated fraction of oil on natural phytoplankton communities was very subtle, undetectable on some occasions, and of much lower magnitude than the effects recorded in microcosm experiments. This suggests that the initial composition of the phytoplankton community determines the degree of response and that the experimental approach adopted could explain the different, and sometimes contradictory, reported responses of the planktonic community to the input of oil into the marine environment.

  12. Is this Diesel mine? Advances in forensic identification using source specific markers of petroleum releases into the environment

    Energy Technology Data Exchange (ETDEWEB)

    Scally, K. [General Manager, Alcontrol Laboratories Ireland, Dublin (Ireland); Nathanail, P. [Nottingham Univ., Course Director, Land Quality Management Group (United Kingdom); Jones, J. [Technical Director, Alcontrol Laboratories Chester (United Kingdom); Keogh, M. [Lecturer in Science, Galway-Mayo Institute of Technology (GMIT) (Ireland); Keaveney, G. [Lecturer in Science, Galway-Mayo Institute of Technology (GMIT), Dublin Road, Galway (Ireland)

    2005-07-01

    Recent developments in forensic hydrocarbon fingerprint analysis have enabled specific markers found in diesel to be characterised and identified. Fingerprinting and data interpretation techniques include the recognition of distribution patterns of hydrocarbons which include the alkylated naphthalene, phenanthrene, dibenzo-thiophene, fluorene, chrysene and phenol isomers; analysis of 'source-specific marker' compounds, individual saturated hydrocarbons, including n-alkanes (n-C{sub 5} through n-C{sub 40}), alkyl-cyclohexane homologues series, and the recalcitrant isoprenoids: pristane and phytane; the determination of diagnostic ratios of specific petroleum and non-petroleum constituents; and the application of various statistical and numerical analysis tools. A spill sample was analysed to identify the possible source and origin of the petroleum contaminant (diesel). Samples were subjected to analysis by gas chromatography, utilising both flame ionisation and time of flight mass spectral detection techniques (TOF-MS) in comparison to known reference materials. The analysis showed the diesel came from the suspected source. This allowed the regulator to prosecute. (authors)

  13. Is this Diesel mine? Advances in forensic identification using source specific markers of petroleum releases into the environment

    International Nuclear Information System (INIS)

    Recent developments in forensic hydrocarbon fingerprint analysis have enabled specific markers found in diesel to be characterised and identified. Fingerprinting and data interpretation techniques include the recognition of distribution patterns of hydrocarbons which include the alkylated naphthalene, phenanthrene, dibenzo-thiophene, fluorene, chrysene and phenol isomers; analysis of 'source-specific marker' compounds, individual saturated hydrocarbons, including n-alkanes (n-C5 through n-C40), alkyl-cyclohexane homologues series, and the recalcitrant isoprenoids: pristane and phytane; the determination of diagnostic ratios of specific petroleum and non-petroleum constituents; and the application of various statistical and numerical analysis tools. A spill sample was analysed to identify the possible source and origin of the petroleum contaminant (diesel). Samples were subjected to analysis by gas chromatography, utilising both flame ionisation and time of flight mass spectral detection techniques (TOF-MS) in comparison to known reference materials. The analysis showed the diesel came from the suspected source. This allowed the regulator to prosecute. (authors)

  14. 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

  15. 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

  16. Plant contamination by organic pollutants in phytoremediation.

    Science.gov (United States)

    Sung, K; Yavuz Corapcioglu, M; Drew, M C; Munster, C L

    2001-01-01

    Phytoremediation is a remediation technique that involves plant uptake, transformation, accumulation, and/or volatilization of soil- and aqueous-phase contaminants or by the stimulation of microbial cometabolic activity in the rhizosphere of the plant. Even when the principal mechanism is by stimulation of bacteria, any resultant plant contamination cannot be overlooked. For the purpose of modeling, a two-compartment plant model has been developed. The model divides the plant into the shoot compartment (which can be harvested) and the root compartment (into which contaminants can accumulate). Numerical experiments were conducted to investigate model behavior and to determine important parameters affecting plant contamination. Johnsongrass [Sorghum halepense (L.) Pers.] was used to evaluate the model behavior. The contaminants TNT (2,4,6,-trinitrotoluene) and chrysene were selected on the basis of their contrasting aqueous-phase solubilities. The results indicate that plant contamination and soil remediation by plants depend on soil properties such as soil organic carbon content, the physicochemical properties of the contaminants such as the octanol-water partition coefficient, and plant properties. The most important factor affecting plant contamination is bioavailability. As bioavailability increased, the concentrations in root and shoot compartments were predicted to increase. Microbial activities and plant contamination are closely related, which suggests that plants and microorganisms can have complementary roles in phytoremediation.

  17. Distribution, Levels, and Risk Assessment of Polycyclic Aromatic Hydrocarbons (PAHs in Some Water Bodies along the Coastal Belt of Ghana

    Directory of Open Access Journals (Sweden)

    David Kofi Essumang

    2010-01-01

    Full Text Available The levels and distribution of 24 polycyclic aromatic hydrocarbons (PAHs were determined in six water bodies along the coastal belt of Ghana using gas chromatography with flame-ionization detection (GC/FID. The average total PAHs recorded are from the Pra estuary, 6.3 μg/L; Benya lagoon, 7.5 μg/L; Sakumono lagoon, 10.1 μg/L; lower Volta estuary, 26.3 μg/L; Keta lagoon, 10.6 μg/L; and Narkwa lagoon, 16.1 μg/L.The 12 PAHs that were well distributed in all the coastal waters analyzed include naphthalene, pyrene, fluorene, 2-methylnaphthalene, 2,6-dimethylnaphthalene, acephnaphthalene, acephnaphthene, 1-methylphenanthrene, 2,3,5-trimethylnaphthalene, chrysene, biphenyl, and phenanthrene. The presence of benzo(bfluoranthene, benzo(aanthracene, and benzo(j,kfluoranthene in some of the water bodies is a source of concern as they have been classified by the International Agency for Research on Cancer (IARC and U.S. Environmental Protection Agency (EPA as probable human carcinogens. These water bodies are used for fishing and for some domestic purposes by the people living around them, thereby exposing them to some dangers and the risk of getting cancer. The human health cancer risk assessment carried out also indicates that there is the possibility of some users of the water bodies getting cancer in their lifetime.

  18. Electromagnetic plasmon propagation and coupling through gold nanoring heptamers: a route to design optimized telecommunication photonic nanostructures.

    Science.gov (United States)

    Ahmadivand, Arash; Golmohammadi, Saeed

    2014-06-20

    In this work, a configuration of bulk gold nanorings with certain geometrical sizes has been utilized for designing efficient photonic subwavelength nanostructures. We verify that adjacent heptamers based on gold nanorings are able to couple and transport magnetic plasmon resonance along a nanoring array in chrysene and triphenylene molecule orientations. This magnetic resonance transmission is caused by an antiphase circular current through the heptamer arrays. An orientation model of nanoring heptamers helps us to provide efficient optical structures with a remarkable decay length and a trivial ratio of destructive interferences. Exploiting the robust magnetic plasmon resonance coupling effect between heptamers arrays, we would be able to propose a practical plasmonic waveguide, a Y-shaped optical power divider (splitter), and an ON/OFF router that is operating based on destructive and constructive interferences. The quality of power splitting has been discussed comprehensively and also, the effect of undesirable occasions on the functioning performance of the proposed router has been investigated numerically. Ultimately, we verify that employing heptamers based on gold nanorings leads us to propose efficient plasmonic nanostructures and devices that are able to work in the telecommunication spectrum.

  19. Collection-efficient, axisymmetric vacuum sublimation module for the purification of solid materials

    Science.gov (United States)

    May, Michael; Paul, Elizabeth; Katovic, Vladimir

    2015-11-01

    A vacuum sublimation module of axisymmetric geometry was developed and employed to purify solid-phase materials. The module provides certain practical advantages and it comprises: a metering valve, glass collector, glass lower body, main seal, threaded bushing, and glass internal cartridge (the latter to contain starting material). A complementary process was developed to de-solvate, sublime, weigh, and collect solid chemical materials exemplified by oxalic acid, ferrocene, pentachlorobenzene, chrysene, and urea. The oxalic acid sublimate was analyzed by titration, melting range, Fourier Transform Infrared (FT-IR) Spectroscopy, cyclic voltammetry, and its (aqueous phase) electrolytically generated gas. The analytical data were consistent with a high-purity, anhydrous oxalic acid sublimate. Cyclic voltammograms of 0.11 mol. % oxalic acid in water displayed a 2.1 V window on glassy carbon electrode beyond which electrolytic decomposition occurs. During module testing, fifteen relatively pure materials were sublimed with (energy efficient) passive cooling and the solid-phase recovery averaged 95 mass %. Key module design features include: compact vertical geometry, low-angle conical collector, uniformly compressed main seal, modest power consumption, transparency, glovebox compatibility, cooling options, and preferential conductive heat transfer. To help evaluate the structural (module) heat transfer, vertical temperature profiles along the dynamically evacuated lower body were measured versus electric heater power: for example, an input of 18.6 W generated a temperature 443-K at the bottom. Experimental results and engineering calculations indicate that during sublimation, solid conduction is the primary mode of heat transfer to the starting material.

  20. Pollution level, phase distribution and health risk of polycyclic aromatic hydrocarbons in indoor air at public places of Hangzhou, China

    Energy Technology Data Exchange (ETDEWEB)

    Lu Hao [Department of Environmental Science, Zhejiang University, Hangzhou, Zhejiang, 310028 (China)], E-mail: luhaozju@163.com; Zhu Lizhong [Department of Environmental Science, Zhejiang University, Hangzhou, Zhejiang, 310028 (China)], E-mail: zlz@zju.edu.cn; Chen Shuguang [Department of Environmental Science, Zhejiang University, Hangzhou, Zhejiang, 310028 (China)], E-mail: chenshuguang@zju.edu.cn

    2008-04-15

    PAHs pollution survey in air of public places was conducted in Hangzhou, China. The most serious PAHs pollution was observed in indoor air of shopping centers and the slightest was in train stations. The molecular weight of chrysene (MW 228) appeared to be the dividing line for the PAHs with a larger or smaller distribution in the vapor or particulate phase. Concentrations of 15 PAHs on PM{sub 2.5} accounted for 71.3% of total particulate PAHs, and followed by PM{sub 2.5-10} fraction (17.6%) and >PM{sub 10} fraction (11.1%). In shopping centers and supermarkets, emission of 2-4 rings PAHs occurred from indoor sources, whereas 5-6 rings PAHs predominantly originated from transport of outdoor air. In temples, PAHs in indoor air mainly originated from incense burning. Health risks associated with the inhalation of PAHs were assessed, and naphthalene made the greatest contribution (62.4%) to the total health risks. - Concentrations of PAHs in the air of selected public places in Hangzhou correspond to 10{sup -3} life-time lung cancer risk.

  1. PAH in tea and coffee

    DEFF Research Database (Denmark)

    Duedahl-Olesen, Lene; Navarantem, Marin; Adamska, Joanna;

    For food regulation in the European Union maximum limits on other foods than tea and coffee includes benzo[a]pyrene and the sum of PAH4 (sum of benzo[a]pyrene, chrysene, benz[a]anthracene and benzo[b]fluoranthene). This study includes analysis of the above mentioned PAH in both, tea leaves, coffee...... for accumulation of PAH in tea leaves. Different varieties of tea leaves were analyzed and highest concentrations were found in leaves from mate and black tea with maximum concentrations of 32 μg/kg for benzo[a]pyrene and 115 μg/kg for the sum of PAH4. Also, coffee beans are roasted during processing. However......, both benzo[a]pyrene and PAH4 concentrations were more than ten times lower for coffee beans than for tea leaves. Highest levels were found for PAH4 of solid instant coffee (5.1 μg/kg). Data were used to calculate the exposure of benzo[a]pyrene (15%) and sum of PAH4 (10%) from tea and coffee...

  2. PAH in Some Brands of Tea and Coffee

    DEFF Research Database (Denmark)

    Duedahl-Olesen, Lene; Navaratnam, Marin Arosha; Jewula, J.;

    2015-01-01

    The presence of 25 polycyclic aromatic hydrocarbons (PAHs) in tea and coffee were investigated with focus on four PAHs (PAH4), classified by the European Food Safety Authority (EFSA) as suitable indicators; benz[a]anthracene (BaA), chrysene (CHR), benzo[b]fluoranthene (BbF) and benzo[a]pyrene (Ba......P). PAH4 from samples of 18 brands of tea leaves and 13 brands of coffee were extracted by pressurized liquid extraction (PLE) followed by highly automated clean up steps for gel permeation chromatography (SX-3) and solid phase extraction (500mg silica). GC-MS were applied for detection of PAH4. The limit...... of detection (LOD) ranged from 0.1–0.3 μg/kg with recoveries from 94–106% for PAH4. Concentrations of PAH4 followed the pattern of the total sum of 25 PAHs with higher concentrations with a maximum of 115 μg/kg in tea leaves compared to 5.1 μg/kg in coffee. The highest PAH4 levels were found in black tea...

  3. Validation of analytical conditions for determination of polycyclic aromatic hydrocarbons in roasted coffee by gas chromatography-mass spectrometry.

    Science.gov (United States)

    Guatemala-Morales, Guadalupe María; Beltrán-Medina, Elisa Alejandra; Murillo-Tovar, Mario Alfonso; Ruiz-Palomino, Priscilla; Corona-González, Rosa Isela; Arriola-Guevara, Enrique

    2016-04-15

    Polycyclic aromatic hydrocarbons (PAHs) are of significant interest due to their genotoxicity in humans. PAHs quantification in coffee is complex since some of its compounds interfere in the chromatographic analysis, which hinders the reliable determination of the PAHs. Analytical conditions for the ultrasound extraction, purification and quantification of 16 PAHs in roasted coffee were studied. The better extraction efficiency of benzo[a]pyrene (68%) from ground-roasted coffee was achieved with a solvent ratio of Hex:MC (9:1 v/v) and three extraction periods of 20 min, followed by alkaline saponification and purification of the extracts. The detection limits were 0.85-39.32 ng mL(-1), and the quantification limits from 2.84 to 131.05 ng mL(-1), obtained for fluoranthene and chrysene, respectively. The extraction was effective for most of the analytes, with recoveries of 39.8% dibenzo[ah]anthracene and 69.0% benzo[b]fluoranthene. For coffee roasted in a spouted bed reactor, the summation of the 16 PAHs ranged from 3.5 to 16.4 μg kg(-1).

  4. 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

  5. Modeling the formation of some polycyclic aromatic hydrocarbons during the roasting of Arabica coffee samples.

    Science.gov (United States)

    Houessou, Justin Koffi; Goujot, Daniel; Heyd, Bertrand; Camel, Valerie

    2008-05-28

    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, for roasting conditions ranging from 5 to 20 min. Several PAHs were determined in both roasted coffee samples and green coffee samples. Different models were tested, with more or less assumptions on the chemical phenomena, with a view to predict the system global behavior. Two kinds of models were used and compared: kinetic models (based on Arrhenius law) and statistical models (neural networks). The numbers of parameters to adjust differed for the tested models, varying from three to nine for the kinetic models and from five to 13 for the neural networks. Interesting results are presented, with satisfactory correlations between experimental and predicted concentrations for some PAHs, such as pyrene, benz[a]anthracene, chrysene, and anthracene. PMID:18433138

  6. Validation of analytical conditions for determination of polycyclic aromatic hydrocarbons in roasted coffee by gas chromatography-mass spectrometry.

    Science.gov (United States)

    Guatemala-Morales, Guadalupe María; Beltrán-Medina, Elisa Alejandra; Murillo-Tovar, Mario Alfonso; Ruiz-Palomino, Priscilla; Corona-González, Rosa Isela; Arriola-Guevara, Enrique

    2016-04-15

    Polycyclic aromatic hydrocarbons (PAHs) are of significant interest due to their genotoxicity in humans. PAHs quantification in coffee is complex since some of its compounds interfere in the chromatographic analysis, which hinders the reliable determination of the PAHs. Analytical conditions for the ultrasound extraction, purification and quantification of 16 PAHs in roasted coffee were studied. The better extraction efficiency of benzo[a]pyrene (68%) from ground-roasted coffee was achieved with a solvent ratio of Hex:MC (9:1 v/v) and three extraction periods of 20 min, followed by alkaline saponification and purification of the extracts. The detection limits were 0.85-39.32 ng mL(-1), and the quantification limits from 2.84 to 131.05 ng mL(-1), obtained for fluoranthene and chrysene, respectively. The extraction was effective for most of the analytes, with recoveries of 39.8% dibenzo[ah]anthracene and 69.0% benzo[b]fluoranthene. For coffee roasted in a spouted bed reactor, the summation of the 16 PAHs ranged from 3.5 to 16.4 μg kg(-1). PMID:26617012

  7. Dibenzofuran Series in Terrestrial Source Rocks and Crude Oils and Applications to Oil-Source Rock Correlations in the Kuche Depression of Tarim Basin, NW China

    Institute of Scientific and Technical Information of China (English)

    李景贵; 李梅; 王兆云

    2004-01-01

    Ten series of aromatic hydrocarbon compounds (biphenyl, naphthalene, phenanthrene, anthracene, retene, chrysene, benzoanthracene, dibenzofuran, fluorene, dibenzothiophene) isolated from seven Triassic and Jurassic lacustrine mudstone samples and three swamp coal samples, as well as five crude oil samples collected in the Kuche depression of the Tarim Basin, NW China, have been analysed by GC-MS techniques. It is found that the relative abundances of dibenzofuran series are higher in the three swamp coal samples than those in the lacustrine mudstone samples. Based on the similar relative abundances of dibenzofuran series, especially dibenzofuran compound, in the TICs of aromatic hydrocarbons, crude oils from wells SA3 (K), YTK5 (E, K) and QL1 (E) are thought to have been derived predominantly from the coals of the Lower Jurassic Yangxia Formation or Middle Jurassic Kezilenuer Formation, whereas those from wells YM7 (O) and YH1 (E) were derived mainly from Triassic and Jurassic lacustrine mudstones in the Kuche depression. This is the first report about how to distinguish coal-generated oils from lacustrine mudstone-generated oils in the Kuche depression in terms of the dibenzofuran series. The present paper has enlightening and directive significance for further oil-source rock correlations and oil and/or gas exploration in the Kuche depression of the Tarim Basin.

  8. Chemical characterization of aromatic compounds in extra heavy gas oil by comprehensive two-dimensional gas chromatography coupled to time-of-flight mass spectrometry.

    Science.gov (United States)

    Avila, Bárbara M F; Pereira, Ricardo; Gomes, Alexandre O; Azevedo, Débora A

    2011-05-27

    Comprehensive two-dimensional gas chromatography coupled to time-of-flight mass spectrometry (GC×GC-TOFMS) was used for the characterization of aromatic compounds present in extra heavy gas oil (EHGO) from Brazil. Individual identification of EHGO compounds was successfully achieved in addition to group-type separation on the chromatographic plane. Many aromatic hydrocarbons, especially polycyclic aromatic hydrocarbons and sulfur compounds, were detected and identified, such as chrysenes, phenanthrenes, perylenes, benzonaphthothiophenes and alkylbenzonaphthothiophenes. In addition, triaromatic steroids, methyl-triaromatic steroids, tetrahydrochrysenes and tetraromatic pentacyclic compounds were present in the EHGO aromatic fractions. Considering the roof-tile effect observed for many of these compound classes and the high number of individual compounds identified, GC×GC-TOFMS is an excellent technique to characterize the molecular composition of the aromatic fraction from EHGO samples. Moreover, data processing allowed the quantification of aromatic compounds, in class and individually, using external standards. EHGO data were obtained in μgg(-1), e.g., benzo[a]pyrene were in the range 351 to 1164μgg(-1). Thus, GC×GC-TOFMS was successfully applied in EHGO quantitative analysis.

  9. Comparison of polycyclic aromatic hydrocarbons level between suspended solid and sediment samples of Pengkalan Chepa River, Kelantan state, Malaysia

    Science.gov (United States)

    Muslim, Noor Zuhartini Md; Babaheidari, Seyedreza Hashemi; Zakaria, Mohamad Pauzi

    2015-09-01

    Sixteen type of common Polycyclic Aromatic Hydrocarbons (PAHs) which consist of naphthalene, acenaphthene, acenaphthylene, fluorene, phenanthrene, anthracene, fluoranthene, pyrene, benz[a]anthracene, chrysene, benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[a]pyrene, benzo[ghi]-perylene, indeno[1,2,3-cd]-pyrene and dibenz[a,h]-anthracene in suspended solid and sediment samples of Pengkalan Chepa River, Kelantan state, Malaysia were investigated. The analysis samples were taken from six different sites of Pengkalan Chepa River during sunny day. The samples were subjected to a series of pre-treatment before the level of PAHs can be determined. A Gas Chromatography-Mass Spectrometry (GC-MS) was the prime method for the analysis of PAHs level. A total of 16 PAHs concentration in suspended solid of the whole Pengkalan Chepa River was found to be 2144.6 ng/g dry weights. This concentration was about eight times more than 16 PAHs concentration in sediment which found to be 266.5 ng/g dry weights.

  10. Sample preparation of sewage sludge and soil samples for the determination of polycyclic aromatic hydrocarbons based on one-pot microwave-assisted saponification and extraction.

    Science.gov (United States)

    Pena, M Teresa; Pensado, Luis; Casais, M Carmen; Mejuto, M Carmen; Cela, Rafael

    2007-04-01

    A microwave-assisted sample preparation (MASP) procedure was developed for the analysis of polycyclic aromatic hydrocarbons (PAHs) in sewage sludge and soil samples. The procedure involved the simultaneous microwave-assisted extraction of PAHs with n-hexane and the hydrolysis of samples with methanolic potassium hydroxide. Because of the complex nature of the samples, the extracts were submitted to further cleaning with silica and Florisil solid-phase extraction cartridges connected in series. Naphthalene, acenaphthene, fluorene, phenanthrene, anthracene, fluoranthene, pyrene, benz[a]anthracene, chrysene, benzo[e]pyrene, benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[a]pyrene, dibenz[a,h]anthracene, benzo[g,h,i]perylene, and indeno[1,2,3-cd]pyrene, were considered in the study. Quantification limits obtained for all of these compounds (between 0.4 and 14.8 microg kg(-1) dry mass) were well below of the limits recommended in the USA and EU. Overall recovery values ranged from 60 to 100%, with most losses being due to evaporation in the solvent exchange stages of the procedure, although excellent extraction recoveries were obtained. Validation of the accuracy was carried out with BCR-088 (sewage sludge) and BCR-524 (contaminated industrial soil) reference materials.

  11. Characterization of particulate polycyclic aromatic hydrocarbons in an urban atmosphere of central-southern Spain.

    Science.gov (United States)

    Villanueva, Florentina; Tapia, Araceli; Cabañas, Beatriz; Martínez, Ernesto; Albaladejo, José

    2015-12-01

    Over 1-year period, 13 polycyclic aromatic hydrocarbons (PAHs) associated with particulate matter PM10 have been monitored for the first time in the atmosphere of Ciudad Real, situated at the central-southern Spain. PM10-bound PAHs were collected using a high-volume sampler from autumn 2012 to summer 2013 and were analyzed by HPLC with fluorescence detector. The most abundant PAHs were pyrene, chrysene, benzo[b]fluoranthene, dibenzo[a,h]anthracene and benzo[g,h,i]perylene. The ∑PAH concentrations in Ciudad Real were 888, 368, 259 and 382 pg m(-3) for winter, spring, summer and autumn seasons, respectively. The diurnal variation of PAH was also investigated presenting the highest concentrations during the evening (19:00-23:00). Benzo[a]pyrene concentrations ranged from 2.4 to 110 pg m(-3), these values are lower than the target value proposed by the European legislation, 1 ng m(-3). Diagnostic ratios were used to identify potential sources of PAHs. Results suggest that vehicle emissions are the major source of identified PAHs, with a higher contribution of diesel engines although other anthropogenic sources could also have an impact on the PAH levels. PMID:26201660

  12. Hydrocarbon analysis using desorption atmospheric pressure chemical ionization

    KAUST Repository

    Jjunju, Fred P M

    2013-07-01

    Characterization of the various petroleum constituents (hydronaphthalenes, thiophenes, alkyl substituted benzenes, pyridines, fluorenes, and polycyclic aromatic hydrocarbons) was achieved under ambient conditions without sample preparation by desorption atmospheric pressure chemical ionization (DAPCI). Conditions were chosen for the DAPCI experiments to control whether ionization was by proton or electron transfer. The protonated molecule [M+H]+ and the hydride abstracted [MH]+ form were observed when using an inert gas, typically nitrogen, to direct a lightly ionized plasma generated by corona discharge onto the sample surface in air. The abundant water cluster ions generated in this experiment react with condensed-phase functionalized hydrocarbon model compounds and their mixtures at or near the sample surface. On the other hand, when naphthalene was doped into the DAPCI gas stream, its radical cation served as a charge exchange reagent, yielding molecular radical cations (M+) of the hydrocarbons. This mode of sample ionization provided mass spectra with better signal/noise ratios and without unwanted side-products. It also extended the applicability of DAPCI to petroleum constituents which could not be analyzed through proton transfer (e.g., higher molecular PAHs such as chrysene). The thermochemistry governing the individual ionization processes is discussed and a desorption/ionization mechanism is inferred. © 2012 Elsevier B.V.

  13. Boron-mediated sequential alkyne insertion and C-C coupling reactions affording extended π-conjugated molecules.

    Science.gov (United States)

    Shoji, Yoshiaki; Tanaka, Naoki; Muranaka, Sho; Shigeno, Naoki; Sugiyama, Haruka; Takenouchi, Kumiko; Hajjaj, Fatin; Fukushima, Takanori

    2016-01-01

    C-C bond coupling reactions illustrate the wealth of organic transformations, which are usually mediated by organotransition metal complexes. Here, we show that a borafluorene with a B-Cl moiety can mediate sequential alkyne insertion (1,2-carboboration) and deborylation/Csp(2)-Csp(2) coupling reactions, leading to aromatic molecules. The first step, which affords a borepin derivative, proceeds very efficiently between the borafluorene and various alkynes by simply mixing these two components. The second step is triggered by a one-electron oxidation of the borepin derivative, which results in the formation of a phenanthrene framework. When an excess amount of oxidant is used in the second step, the phenanthrene derivatives can be further transformed in situ to afford dibenzo[g,p]chrysene derivatives. The results presented herein will substantially expand the understanding of main group chemistry and provide a powerful synthetic tool for the construction of a wide variety of extended π-conjugated systems. PMID:27581519

  14. Macondo oil in deep-sea sediments: Part 1 - sub-sea weathering of oil deposited on the seafloor.

    Science.gov (United States)

    Stout, Scott A; Payne, James R

    2016-10-15

    Chemical analysis of sediment cores collected up to 8km from the Macondo well in 2010/2011 demonstrates the extent of weathering of the Macondo oil deposited in deep-sea sediments following the Deepwater Horizon disaster. On average, dissolution and biodegradation of the oil on the seafloor increased with distance from the well indicating that weathering occurred rapidly and overwhelmingly during the oil's transport as dispersed oil droplets within the deep-sea plume. Beyond about 5km from the well, the oil deposited on the seafloor had lost most mass below C25, was relatively enriched in n-C25+ n-alkanes and C3- and C4-alkylated benz[a]anthracenes/chrysenes, the latter owing to 95% depletion of total PAHs. Biodegradation of C28 and C29 tricyclic terpanes, C34 and C35 17α(H),21β(H)-homohopanes, C27 13β(H),17α(H)-dia and C27 14β(H),17β(H)-steranes and dissolution of C26 to C28 triaromatic steroids occurred. The results provide a means to distinguish Macondo oil in deep-sea sediments from naturally-occurring seep oils and pervasive ambient background hydrocarbons.

  15. New observations on PAH pollution in old heavy industry cities in northeastern China.

    Science.gov (United States)

    Song, Ningning; Ma, Junhua; Yu, Yang; Yang, Zhifeng; Li, Yingxia

    2015-10-01

    This study investigated the distinctive PAHs adsorbed on street dust near various industries in the three typical industrialized cities of Daqing (DQ), Harbin (HEB) and Jilin (JL) in northeastern China. The mean ∑PAHs concentrations in street dust of DQ, HEB and JL were 1.84, 4.87, 12.38 μg/g, respectively. Typical petroleum resource city DQ had higher proportions of low and medium ringed PAHs with higher proportions of phenanthrene (Phe), naphthalene (Nap), fluoranthene (Flua) and chrysene (Chr) at industrial sites. Typical chemical processing city JL had higher proportions of medium and high ringed PAHs with higher proportions of Flua, benz[a]anthracene (BaA), pyrene (Pyr) and benzo[a]pyrene (BaP) at industrial sites. Phe, Flua, Pyr and Chr were four major PAHs from most studied industries. The distinctive PAH emissions from the ferroalloy plant were BaA and BaP. BaA and BaP concentrations decreased by 90% at sites more than 2 km away from the ferroalloy plant.

  16. Distribution and Health Risk Assessment of Polycyclic Aromatic Hydrocarbons in Soil from a Typical Contaminated Urban Coking Sites in Shenyang City.

    Science.gov (United States)

    Hou, Wei; Zhang, Le; Li, Yue; Zhang, Lihong; Li, Shuxian; Ji, Lan; Dan, Su

    2015-12-01

    This study evaluated the level of PAH pollution in typical contaminated coking sites in Shenyang. Sixty surface soil samples were collected from an area of 1.3 × 10(5) m(2) polluted by PAHs. The concentrations, sources and possible health risks of 16 PAHs in the area were analyzed. The average content of Σ16 PAHs was 6.1 × 10(3) mg/kg. In oral intake, benzo(a)pyrene (BaP) presented the largest exposure risk (hazard quotient HQ = 1.17 × 10(-5)), followed by dibenz(a,h)anthracene (DbA) (HQ = 1.14 × 10(-5)). The non-carcinogenic hazard indices and carcinogenic risks of the PAHs were arranged in the order of BaP > DbA > benzo(b)fluoranthene (BbF) > benz(a)anthracene (BaA) > indeno(1,2,3-cd)pyrene (InP) > benzo(k)fluoranthene (BkF) > chrysene (Chr). Bap and DbA were the principal pollution sources, followed by BbF, BaA, InP, BkF and Nap successively. Oral intake was the main route of PAH entry into the human body. PMID:26508427

  17. 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.

  18. Metabolism and macromolecular binding of benzo(a)pyrene and its noncarcinogenic isomer benzo(e)pyrene in cell culture

    Energy Technology Data Exchange (ETDEWEB)

    Selkirk, J.K.; MacLeod, M.C.

    1978-01-01

    The carcinogenicity of the polycyclic aromatic hydrocarbon benzo(a)pyrene (B(a)P) is thought to result from the metabolic formation of a highly reactive intermediate, 7,8-dihydrodiol-9,10-oxy-B(a)P which subsequently interacts with cellular macromolecules to produce neoplasia. Evidence has been presented implicating similar bay-region diol-epoxides as the ultimate carcinogenic forms of benz(a)anthracene, 7-methyl-benz(a)anthracene, dibenz(a,h)anthracene, and chrysene. Benzo(e)pyrene (B(e)P), on the other hand, is relatively inert when tested for carcinogenicity on mouse skin and rat trachea and when tested for mutagenicity in a mammalian system. This B(e)P molecule contains two (equivalent) bay regions and quantum mechanical model calculations suggest that 9,10-dihydrodiol-11,12-oxy-B(e)P can easily form a reactive bay-region-adjacent carbonium ion. In order to explain the noncarcinogenicity of B(e)P in the context of the bay region theory, we have studied the metabolism of B(e)P by rat liver microsomes and by cultured hamster embryo fibroblasts. In both systems, the major metabolic pathways involve the K-region of B(e)P, with little or no attack on the isolated benzo ring. These results suggest that the lack of carcinogenicity of B(e)P may reflect its preferred mode of interaction with the cellular metabolic machinery.

  19. Simultaneous analysis of phthalates, adipate and polycyclic aromatic hydrocarbons in edible oils using isotope dilution-gas chromatography-mass spectrometry.

    Science.gov (United States)

    Oh, Min-Seok; Lee, Seon-Hwa; Moon, Myeong Hee; Lee, Dong Soo; Park, Hyun-Mee

    2014-01-01

    A method for simultaneous determination of 12 priority phthalates, adipate and polycyclic aromatic hydrocarbons (PAHs) in edible oils by isotope dilution-gas chromatography-mass spectrometry (ID-GC-MS) was developed for fast, accurate and trace analysis. The extraction and clean-up procedures were optimised, and using stable isotope-labelled internal standards for each analyte, relative standard deviations (RSDs) of 0.92-10.6% and spiked sample recoveries of 80.6-97.8% were obtained. Limits of detection for PAHs were in the range of 0.15-0.77 µg/kg and those for phthalates were in the range of 4.6-10.0 µg/kg. The calibration curves exhibited good linearities with regression coefficients of R(2) ≥ 0.99. Twelve edible oils were examined to evaluate the efficiency of this method. Among the 12 analytes, dibutyl phthalates (DBP), diethylhexyl phthalates (DEHP), diethylhexyl adipate (DEHA), benzo[a]anthracene (B[a]A), chrysene (Chry) and benzo[b]fluoranthene (B[b]F) were detected in the range of 1.17-806 µg/kg.

  20. Effects of storage on sediment toxicity, bioaccumulation potential, and chemistry. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Tatem, H.E.; Brandon, D.L.; Lee, C.R.; Jarvis, A.S.; Rhett, R.G.

    1991-01-01

    Current guidance on storage of sediments for bioassay/bioaccumulation tests requires that samples be held at 4 C and used within 2 weeks of collection. The objective of this study was to determine the effects of sediment storage for 40 weeks on sediment toxicity, bioaccumulation potential, and chemical analyses. Toxicity and bioaccumulation tests were conducted five times during 40 weeks of storage. Chemical analyses were performed three times during this period. The data indicate that sediments can be held for longer than 2 to 4 weeks, in many cases, without significant effect on test results. However, results of the study also show that tests performed at different times can produce different results. This study showed that a sediment that was toxic to mysids remained toxic during 16 weeks of sediment storage. Two sediments that were toxic initially continued to show significant toxicity after 8 and 16 weeks of sediment storage. One sediment, not toxic initially or at 4 weeks, changed during storage, becoming significantly toxic compared to the Atlantic Ocean (Ref) sediment. The bioaccumulation results showed that certain sediment contaminants (lead, mercury, polychlorinated biphenyls, and some polycyclic aromatic hydrocarbons, PAHs), generally do not reveal a statistical change in bioaccumulation, relative to Ref animals, during 16 weeks of sediment storage. Other PAHs, including phenanthrene, anthracene, benzo (a) anthracene, and chrysene, did change in bioaccumulation potential during storage.

  1. Mechanistic investigation into the formation of polycyclic aromatic hydrocarbons from the pyrolysis of plant steroids

    Energy Technology Data Exchange (ETDEWEB)

    Britt, P.F.; Buchanan, A.C. III; Kidder, M.M.; Owens, C.; Ammann, J.R.; Skeen, J.T.; Luo, L. [Oak Ridge National Lab., Oak Ridge, TN (United States). Chemical and Analytical Sciences

    2001-10-09

    There have been many studies on the pyrolysis of biomass model compounds but most have not been performed under the high heating rate, short residence time conditions currently used in the thermochemical conversion of biomass. In this investigation, the pyrolysis of plant steroids is investigated by flash vacuum pyrolysis (FVP) and flow pyrolysis at residence times of 0.1-2.0 s and temperatures of 550-800{degree}C to determine if the native cyclic ring structure in the steroid leads to the formation of polycyclic aromatic hydrocarbons (PAHs) or whether PAHs are formed by pyrosynthesis. FVP of stigmasterol stigmasterol acetate, {beta}-sitosterol and stigmasta-3,5-diene at 700{degree}C showed that PAHs, such as acenaphthylene, phenanthrene, anthracene, pyrene, chrysene, benz(a)anthracene, and their monomethylated derivatives were formed in the absence of bimolecular reactions, and the yield of PAHs was dependent of the structure of the steroid. Similar products were found in the flow pyrolysis of stigmasterol, and the yields of PAHs were found to increase with increasing temperature and residence time. Thermochemical kinetic estimates were used to postulate pathways for the formation of the primary pyrolysis products. 66 refs., 9 figs., 7 tabs.

  2. Distribution and Health Risk Assessment of Polycyclic Aromatic Hydrocarbons in Soil from a Typical Contaminated Urban Coking Sites in Shenyang City.

    Science.gov (United States)

    Hou, Wei; Zhang, Le; Li, Yue; Zhang, Lihong; Li, Shuxian; Ji, Lan; Dan, Su

    2015-12-01

    This study evaluated the level of PAH pollution in typical contaminated coking sites in Shenyang. Sixty surface soil samples were collected from an area of 1.3 × 10(5) m(2) polluted by PAHs. The concentrations, sources and possible health risks of 16 PAHs in the area were analyzed. The average content of Σ16 PAHs was 6.1 × 10(3) mg/kg. In oral intake, benzo(a)pyrene (BaP) presented the largest exposure risk (hazard quotient HQ = 1.17 × 10(-5)), followed by dibenz(a,h)anthracene (DbA) (HQ = 1.14 × 10(-5)). The non-carcinogenic hazard indices and carcinogenic risks of the PAHs were arranged in the order of BaP > DbA > benzo(b)fluoranthene (BbF) > benz(a)anthracene (BaA) > indeno(1,2,3-cd)pyrene (InP) > benzo(k)fluoranthene (BkF) > chrysene (Chr). Bap and DbA were the principal pollution sources, followed by BbF, BaA, InP, BkF and Nap successively. Oral intake was the main route of PAH entry into the human body.

  3. 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

  4. Hydrocarbon status of soils under atmospheric pollution from a local industrial source

    Science.gov (United States)

    Gennadiev, A. N.; Zhidkin, A. P.; Pikovskii, Yu. I.; Kovach, R. G.; Koshovskii, T. S.; Khlynina, N. I.

    2016-09-01

    Contents and compositions of bitumoids, polycyclic aromatic hydrocarbons (PAHs), and free and retained hydrocarbon gases in soils along a transect at different distances from the local industrial source of atmospheric pollution with soot emissions have been studied. The reserves of PAHs progressively decrease when the distance from the source increases. Among the individual PAHs, the most significant decrease is observed for benzo[ a]pyrene, tetraphene, pyrene, chrysene, and anthracene. On plowlands, the share of heavy PAHs—benzo[ ghi]perylene, benzo[ a]pyrene, perylene, etc.—is lower than in the forest soils. In automorphic soils of the park zone adjacent to the industrial zone, the penetration depth of four-, five-, and sixring PAHs from the atmosphere is no more than 25 cm. In soils under natural forest vegetation, heavy PAHs do not penetrate deeper than 5 cm; in tilled soils, their penetration depth coincides with the lower boundary of plow horizons. Analysis of free gases in the soil air revealed hydrocarbons only under forest. From the quantitative and qualitative parameters of the content, reserves, and compositions of different hydrocarbons, the following modification types of hydrocarbon status in the studied soils were revealed: injection, atmosedimentation-injection, atmosedimentation-impact, atmosedimentation-distant, and biogeochemical types.

  5. Pelagic tar, dissolved/dispersed petroleum hydrocarbons and plastic distribution in the Cretan Sea, Greece

    International Nuclear Information System (INIS)

    During the first cruise of R/V 'Philia' in July 1997 within the framework of the TALOS programme supported by the Greek Ministry of Physical Planning and Public Works, the sampling of floating tar, litter and sea water for dissolved/dispersed petroleum hydrocarbons (DDPH) was carried out in the Cretan Sea. Analysis of these data has allowed a first assessment of the status of floating marine pollution in the region. DDPH measurements showed a mean concentration of 0.145 μg/l of chrysene equivalents (n = 24). Tar and plastics concentrations were in the range of 1-4280 and 0-1160 μg/m2, respectively. Mean pelagic tar concentration was 318 μg/m2, more than two times higher than what was reported for the area in previous studies. Based on in situ hydrographic observations there is strong evidence that most of the floating tar enters the Cretan Sea through the Ionian Sea. (author)

  6. Polycyclic aromatic hydrocarbons in commercial squids from different geographical origins: levels and risks for human consumption.

    Science.gov (United States)

    Gomes, Filipa; Oliveira, Marta; Ramalhosa, Maria João; Delerue-Matos, Cristina; Morais, Simone

    2013-09-01

    The concentrations of 18 polycyclic aromatic hydrocarbons (PAHs) were determined in five commercially valuable squid species from different geographical origins (Atlantic, Indic and Pacific Oceans). Out of the 18 quantified PAHs (the 16 PAHs considered by US EPA as priority pollutants, dibenzo(a,l)pyrene and benzo(j)fluoranthene) only dibenz(a,h)anthracene was not detected. The total concentrations of PAHs varied by a factor of more than 100-fold, from 0.22 (Loligo gahi) to 60.9 μg/kg ww (Loligo reynaudii). Intra- and inter-specific variability of PAH levels was statistically assessed. Nine carcinogenic (probable/possible) PAHs accounted for 1% (L. reynaudii) to 26% (Loligo opalescens) of the total PAHs content being the main contributors naphthalene (in Loligo duvaucelii, L. reynaudii and Loligo vulgaris species), chrysene (in L. opalescens) and indeno(1,2,3-cd)pyrene (in L. gahi). PAHs source analysis indicated that four of the five zones of capture of the different squid species are significantly affected by both petrogenic and pyrolytic sources. Assessment of the target carcinogenic risks, established by the US EPA, suggested that L. gahi (Atlantic Ocean) and L. opalescens (from Pacific Ocean) may pose additional risks for consumers, if not eaten in moderation, derived from benzo(a)pyrene ingestion.

  7. Phytoremediation of mixed-contaminated soil using the hyperaccumulator plant Alyssum lesbiacum: Evidence of histidine as a measure of phytoextractable nickel

    Energy Technology Data Exchange (ETDEWEB)

    Singer, Andrew C. [Centre for Ecology and Hydrology-Oxford, Mansfield Road, Oxford OX1 3SR (United Kingdom)]. E-mail: acsi@ceh.ac.uk; Bell, Thomas [Department of Zoology, University of Oxford, South Parks Road, Oxford OX1 3PS (United Kingdom); Heywood, Chloe A. [Centre for Ecology and Hydrology-Oxford, Mansfield Road, Oxford OX1 3SR (United Kingdom); Smith, J.A.C. [Department of Plant Sciences, University of Oxford, South Parks Road, Oxford OX1 3RB (United Kingdom); Thompson, Ian P. [Centre for Ecology and Hydrology-Oxford, Mansfield Road, Oxford OX1 3SR (United Kingdom)

    2007-05-15

    In this study we examine the effects of polycyclic aromatic hydrocarbons (PAHs) on the ability of the hyperaccumulator plant Alyssum lesbiacum to phytoextract nickel from co-contaminated soil. Planted and unplanted mesocosms containing the contaminated soils were repeatedly amended with sorbitan trioleate, salicylic acid and histidine in various combinations to enhance the degradation of two PAHs (phenanthrene and chrysene) and increase nickel phytoextraction. Plant growth was negatively affected by PAHs; however, there was no significant effect on the phytoextraction of Ni per unit biomass of shoot. Exogenous histidine did not increase nickel phytoextraction, but the histidine-extractable fraction of soil nickel showed a high correlation with phytoextractable nickel. These results indicate that Alyssum lesbiacum might be effective in phytoextracting nickel from marginally PAH-contaminated soils. In addition, we provide evidence for the broader applicability of histidine for quantifying and predicting Ni phytoavailability in soils. - Alyssum lesbiacum was shown to phytoextract nickel from PAH-contaminated soils from which the pool of nickel accessed for phytoextraction is closely modelled by a histidine-soil extract.

  8. Senyawa polisiklik aromatik hidrokarbon (PAH dalam air laut di Teluk Jakarta

    Directory of Open Access Journals (Sweden)

    Edward

    2014-12-01

    Full Text Available Research on polycyclic aromatic hydrocarbons (pahs compound at Jakarta Bay seawater were carried out on July 2011. The objectives of this research were to measure the concentration of total polycyclic aromatic hydrocarbons (PAH compound, concentration of individual PAH compound, and to identify sources of PAH compound in seawater. PAH compound concentration was measured by Gas Chromatography (Gas Chromatography-Flame Ionization Detector and sources of polycyclic aromatic hydrocarbons compound were identified by diagnostic ratio analysis. The results show that the concentration of PAH compound in the middle of Jakarta Bay was higher compared to the west and the east. In the west and middle of Jakarta Bay, it is found that 11 PAH types, and 10 types in the east. Individual PAH compound dominated by high moleculer weight of PAH Benzo(aAnthracene, Chrysene, Benzo(bFluoranthene, Benzo(aPyrene, dan Indeno(123-cd Pyrene. The results of PAH compound ratio individual analysis showed that polycyclic aromatic hydrocarbons compound at Jakarta Bay seawater came from oil spill and incomplete combustion mixture of organic material such as wood, grass, fuel oil, and fuel industry combustion activity.

  9. Senyawa polisiklik aromatik hidrokarbon (PAH dalam air laut di Teluk Jakarta

    Directory of Open Access Journals (Sweden)

    Edward .

    2014-01-01

    Full Text Available Research on polycyclic aromatic hydrocarbons (pahs compound at Jakarta Bay seawater were carried out on July 2011. The objectives of this research were to measure the concentration of total polycyclic aromatic hydrocarbons (PAH compound, concentration of individual PAH compound, and to identify sources of PAH compound in seawater. PAH compound concentration was measured by Gas Chromatography (Gas Chromatography-Flame Ionization Detector and sources of polycyclic aromatic hydrocarbons compound were identified by diagnostic ratio analysis. The results show that the concentration of PAH compound in the middle of Jakarta Bay was higher compared to the west and the east. In the west and middle of Jakarta Bay, it is found that 11 PAH types, and 10 types in the east. Individual PAH compound dominated by high moleculer weight of PAH Benzo(aAnthracene, Chrysene, Benzo(bFluoranthene, Benzo(aPyrene, dan Indeno(123-cd Pyrene. The results of PAH compound ratio individual analysis showed that polycyclic aromatic hydrocarbons compound at Jakarta Bay seawater came from oil spill and incomplete combustion mixture of organic material such as wood, grass, fuel oil, and fuel industry combustion activity.

  10. Boron-mediated sequential alkyne insertion and C–C coupling reactions affording extended π-conjugated molecules

    Science.gov (United States)

    Shoji, Yoshiaki; Tanaka, Naoki; Muranaka, Sho; Shigeno, Naoki; Sugiyama, Haruka; Takenouchi, Kumiko; Hajjaj, Fatin; Fukushima, Takanori

    2016-01-01

    C–C bond coupling reactions illustrate the wealth of organic transformations, which are usually mediated by organotransition metal complexes. Here, we show that a borafluorene with a B–Cl moiety can mediate sequential alkyne insertion (1,2-carboboration) and deborylation/Csp2–Csp2 coupling reactions, leading to aromatic molecules. The first step, which affords a borepin derivative, proceeds very efficiently between the borafluorene and various alkynes by simply mixing these two components. The second step is triggered by a one-electron oxidation of the borepin derivative, which results in the formation of a phenanthrene framework. When an excess amount of oxidant is used in the second step, the phenanthrene derivatives can be further transformed in situ to afford dibenzo[g,p]chrysene derivatives. The results presented herein will substantially expand the understanding of main group chemistry and provide a powerful synthetic tool for the construction of a wide variety of extended π-conjugated systems. PMID:27581519

  11. Collection-efficient, axisymmetric vacuum sublimation module for the purification of solid materials.

    Science.gov (United States)

    May, Michael; Paul, Elizabeth; Katovic, Vladimir

    2015-11-01

    A vacuum sublimation module of axisymmetric geometry was developed and employed to purify solid-phase materials. The module provides certain practical advantages and it comprises: a metering valve, glass collector, glass lower body, main seal, threaded bushing, and glass internal cartridge (the latter to contain starting material). A complementary process was developed to de-solvate, sublime, weigh, and collect solid chemical materials exemplified by oxalic acid, ferrocene, pentachlorobenzene, chrysene, and urea. The oxalic acid sublimate was analyzed by titration, melting range, Fourier Transform Infrared (FT-IR) Spectroscopy, cyclic voltammetry, and its (aqueous phase) electrolytically generated gas. The analytical data were consistent with a high-purity, anhydrous oxalic acid sublimate. Cyclic voltammograms of 0.11 mol. % oxalic acid in water displayed a 2.1 V window on glassy carbon electrode beyond which electrolytic decomposition occurs. During module testing, fifteen relatively pure materials were sublimed with (energy efficient) passive cooling and the solid-phase recovery averaged 95 mass %. Key module design features include: compact vertical geometry, low-angle conical collector, uniformly compressed main seal, modest power consumption, transparency, glovebox compatibility, cooling options, and preferential conductive heat transfer. To help evaluate the structural (module) heat transfer, vertical temperature profiles along the dynamically evacuated lower body were measured versus electric heater power: for example, an input of 18.6 W generated a temperature 443-K at the bottom. Experimental results and engineering calculations indicate that during sublimation, solid conduction is the primary mode of heat transfer to the starting material. PMID:26628150

  12. 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.

  13. Laboratory and field verification of a method to estimate the extent of petroleum biodegradation in soil.

    Science.gov (United States)

    Douglas, Gregory S; Hardenstine, Jeffery H; Liu, Bo; Uhler, Allen D

    2012-08-01

    We describe a new and rapid quantitative approach to assess the extent of aerobic biodegradation of volatile and semivolatile hydrocarbons in crude oil, using Shushufindi oil from Ecuador as an example. Volatile hydrocarbon biodegradation was both rapid and complete-100% of the benzene, toluene, xylenes (BTEX) and 98% of the gasoline-range organics (GRO) were biodegraded in less than 2 days. Severe biodegradation of the semivolatile hydrocarbons occurred in the inoculated samples with 67% and 87% loss of the diesel-range hydrocarbons (DRO) in 3 and 20 weeks, respectively. One-hundred percent of the naphthalene, fluorene, and phenanthrene, and 46% of the chrysene in the oil were biodegraded within 3 weeks. Percent depletion estimates based on C(30) 17α,21β(H)-hopane (hopane) underestimated the diesel-range organics (DRO) and USEPA 16 priority pollutant PAH losses in the most severely biodegraded samples. The C(28) 20S-triaromatic steroid (TAS) was found to yield more accurate depletion estimates, and a new hopane stability ratio (HSR = hopane/(hopane + TAS)) was developed to monitor hopane degradation in field samples. Oil degradation within field soil samples impacted with Shushufindi crude oil was 83% and 98% for DRO and PAH, respectively. The gas chromatograms and percent depletion estimates indicated that similar levels of petroleum degradation occurred in both the field and laboratory samples, but hopane degradation was substantially less in the field samples. We conclude that cometabolism of hopane may be a factor during rapid biodegradation of petroleum in the laboratory and may not occur to a great extent during biodegradation in the field. We recommend that the hopane stability ratio be monitored in future field studies. If hopane degradation is observed, then the TAS percent depletion estimate should be computed to correct for any bias that may result in petroleum depletion estimates based on hopane.

  14. Nonradiological chemical pathway analysis and identification of chemicals of concern for environmental monitoring at the Hanford Site

    International Nuclear Information System (INIS)

    Pacific Northwest's Surface Environmental Surveillance Project (SESP) is an ongoing effort tot design, review, and conducted monitoring on and off the Hanford site. Chemicals of concern that were selected are listed. Using modeled exposure pathways, the offsite cancer incidence and hazard quotient were calculated and a retrospective pathway analysis performed to estimate what onsite concentrations would be required in the soil for each chemical of concern and other detected chemicals that would be required to obtain an estimated offsite human-health risk of 1.0E-06 cancer incidence or 1.0 hazard quotient. This analysis indicates that current nonradiological chemical contamination occurring on the site does not pose a significant offsite human-health risk; the highest cancer incidence to the offsite maximally exposed individual was from arsenic (1.76E-10); the highest hazard quotient was chromium(VI) (1.48E-04). The most sensitive pathways of exposure were surfacewater and aquatic food consumption. Combined total offsite excess cancer incidence was 2.09E-10 and estimated hazard quotient was 2.40E-04. Of the 17 identified chemicals of concern, the SESP does not currently (routinely) monitor arsenic, benzo(a)pyrene, bis(2- ethylhexyl)phthalate (BEHP), and chrysene. Only 3 of the chemicals of concern (arsenic, BEHP, chloroform) could actually occur in onsite soil at concern high enough to cause a 1.0E-06 excess cancer incidence or a 1.0 hazard index for a given offsite exposure pathway. During the retrospective analysis, 20 other chemicals were also evaluated; only vinyl chloride and thallium could reach targeted offsite risk values

  15. Content determination and health risk assessment of polycyclic aromatic hydrocarbon in fish tissue samples from Perhentian Island, Malaysia

    International Nuclear Information System (INIS)

    The concentration of polycyclic aromatic hydrocarbon (PAH) in three fish species with different feeding habits and habitat for examples Lolong (Selar boops), Kerisi (Nemipterus peronii) dan Mengkarong (Trachinocephalus myops) from offshore of Perhentian Island, Malaysia was determined. Three individuals from each species were taken at random and the PAHs contents were determined in the muscles. Ten PAH compounds, phenanthrene, anthracene, fluoranthene, pyrene, benzo(a)anthracene, chrysene, benzo(b)fluoranthene, benzo(k)fluoranthene, benzo(e)pyrene and dibenzo(a,h)anthracene were determined. PAH in fish tissues was extracted using Soxhlet method and detected using gas chromatography - mass spectrometry (GC-MS). The level of PAH in fish tissue ranged from 17.89 - 42.18 ng/ g wet weight and 393.98 - 511.07 ng/ g lipid weight. The order of PAH concentration in wet weight was Kerisi (511.07 ng/ g)> Mengkarong (409.50 ng/ g)> Lolong (393.98 ng/ g) but in terms of lipid weight, the order was Kerisi (511.07 ng/ g)> Mengkarong (409.50 ng/ g)> Lolong (393.98 ng/ g). Kerisi has the lowest lipid content of 3.5 % compared to Lolong (6.5 %) and Mengkarong (10.3 %). No obvious significant difference (p > 0.05) of PAH levels in three fish species was observed (ANOVA, p > 0.05). There was no significant relationship between lipid content and PAH accumulation in fish. Based on fish consumption rate of 142.2 g/ day, the Potency Equivalent Concentration (PEC), which is a carcinogenic potency value for PAH, was found to be ranged from 0.41 - 0.63 ng/ g wet weight in all three species of fish. This value is below the limit set by USEPA, which is 0.67 ng/ g wet weight for human consumption. (author)

  16. 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.

  17. Polycyclic Aromatic Hydrocarbon Concentration Levels on the Korean Peninsula between 2006 and 2008

    Directory of Open Access Journals (Sweden)

    Hang Thi Nguyen

    2010-01-01

    Full Text Available Concentrations of seven polycyclic aromatic hydrocarbon (PAH compounds — benzo(aanthracene (BaA, chrysene (CHRY, benzo(bfluoranthene (BbF, benzo(kfluoranthene (BkF, dibenz(a,hanthracene (DahA, indeno(1,2,3-cdpyrene (I123P, and benzo(apyrene (BaP — in air were measured as the sum of gas and particle fractions at 32 monitoring stations dispersed across Korea during a 2-year period (February 2006 to January 2008. The data sets were collected at intervals of 1 day (24 h per month from each monitoring station. According to our analysis, the spatial distribution of PAH is distinguished by manmade activities between different land use types. Evaluation of total PAH (T-PAH concentration levels, which were derived by summing up all individual compounds, revealed that the T-PAH value varied on the order of commercial (4.85 ± 4.40 ng m-3 rural (4.42 ± 2.73 ng m-3, industrial (4.27 ± 1.79 ng m-3, greenland (3.09 ± 3.86 ng m-3, and background (2.60 ± 2.54 ng m-3 areas. The PAH values, when compared across seasons, tend to peak consistently during the winter (or spring due to the active consumption of fossil fuels. The overall results of this study confirm that the pollution status of PAH compounds are clearly discernible not only between areas with different levels of anthropogenic activities, but also between periods with changes in environmental conditions.

  18. Phytoassessment of a 5-Month Old Waste Engine Oil Polluted Soil after Augmentation with Pleurotus tuberregium

    Directory of Open Access Journals (Sweden)

    Beckley Ikhajiagbe

    2012-01-01

    Full Text Available The present study is a bioassessment of the effects of of substrate microbial augmentation on the bioremediation of Waste Engine Oil (WEO polluted soil. Four different concentrations of WEO in soil on weight basis were obtained by thoroughly mixing WEO in measured soil: 1.0, 2.5, 5.0, and 10.0% w/w. The unpolluted soil was used as the control (0% w/w experiment. The set up was left for 5 months without physically disturbing the soil. After 5 months, the soils were first amended with sawdust and then inoculated with mycelia of Pleurotus tuberregium. Nine months after bioaugmentation (9 MAB there was total (100% remediation of some PAH compounds (benzo(aanthracene, benzo(apyrene, benzo(bfluoranthene, benzo(g,h,iperylene, benzo(kfluoranthene, chrysene, dibenzo(a,hanthracene, fluoranthene, fluorene, and indeno(1,2,3-c,dpyrene was recorded. Significant (p = 0.05 decreases in heavy metal concentration from 5-9 MAB resulted in significant reductions in Hazard Quotients (HQ, which implied less possibility for ecological risk for heavy metal constituents. Phytoassessment of the polluted soil was carried at 5MAP, and results showed that virtually all the cowpea seedlings died within 2 weeks. Only those seedlings in unpolluted soils survived. Nine months after readjustment of soil treatments, all cowpea plants survived up to fruiting, with grain yields in the most polluted soil being 15.25 g/plant compared to 26.01 g/plant in the control experiment. Although heavy metals were minimally accumulated in leaves and seeds of cowpea, bioaccumulation was not significant when Bioaccumulation Quotients (BQ were computed, with BQ value ranges as 0.01-0.05 in seeds and 0.0 -0.80 in leaves. Hydrocarbons was detected in cowpea leaves but not in the seeds.

  19. Soil pollution by PAHs in urban soils: a comparison of three European cities.

    Science.gov (United States)

    Morillo, E; Romero, A S; Maqueda, C; Madrid, L; Ajmone-Marsan, F; Grcman, H; Davidson, C M; Hursthouse, A S; Villaverde, J

    2007-09-01

    The purpose of this study was to determine the degree of contamination with polycyclic aromatic hydrocarbons (PAHs) in samples of urban soil from three European cities: Glasgow (UK), Torino (Italy) and Ljubljana (Slovenia). Fifteen PAHs (naphthalene, acenaphthene, fluorene, phenanthrene, anthracene, fluoranthene, pyrene, benzo[a]anthracene, chrysene, benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[a]pyrene, dibenzo[a,h]anthracene, benzo[g,h,i]perylene, indeno[1,2,3-c,d]pyrene) were measured in urban soil samples, using harmonised sampling, sample extraction and analyte quantification methods. Although the mean concentration of each PAH in urban soils of each city showed a wide range of values, high levels of contamination were only evident in Glasgow, where the sum of concentrations of 15 PAHs was in the range 1487-51,822 microg kg(-1), cf. ranges in the other two cities were about ten-fold lower (89.5-4488 microg kg(-1)). The three predominant PAHs were phenanthrene, fluoranthene and pyrene, with the sum of these compounds about 40% of the total PAH content. These data, together with some special molecular indices based on ratios of selected PAHs, suggest pyrogenic origins, especially motor vehicle exhausts, to be the major sources of PAHs in urban soils of the three cities. The largest concentrations for PAHs were often found in sites close to the historic quarters of the cities. Overall, the different climatic conditions, the organic carbon contents of soil, and the source apportionment were the dominant factors affecting accumulation of PAHs in soil. PMID:17726562

  20. Analysis of Polycyclic Aromatic Hydrocarbons in Cigarette Smoke%卷烟烟气中多环芳烃的分析方法

    Institute of Scientific and Technical Information of China (English)

    张国安; 王复; 李桂贞; 谢焰; 杜向东

    2001-01-01

    通过二次柱层析纯化和富集卷烟烟气中多环芳烃,用气相色谱/质谱法进行多环芳烃的定性和定量分析。在卷烟烟气中检测了蒽,菲,荧蒽,芘,苯并[a]蒽,FDD8,苯并荧蒽,苯并[e]芘,苯并[a]芘等多环芳烃,其浓度在8~391ng/支之间,多环芳烃回收率在80%以上。在此基础上测定了3种不同焦油含量的卷烟烟气中的多环芳烃,发现卷烟烟气中多环芳烃含量与焦油含量有良好的相关性。%Polycyclic aromatic hydrocarbons (PAHs) in cigarette smoke were purified and enriched using flash column chromatography, and then measured by GC-MS. Anthracene, phenanthrene, fluoranthene, pyrene, benzo[a] anthracene, chrysene, benzofluoranthene, benzo[e] pyrene and benzo[a] pyrene in cigarette smoke were analyzed, and their concentrations were found to be 8~391 ng/cigarette. Recovery of PAHs was over 80%. Cigarettes of 3 different tar levels were measured and excellent interdependency was found between PAHs concentration and tar level.

  1. Assessing the long-term weathering of petroleum on shorelines : uses of conserved components for calibrating loss and bioremediation potential

    Energy Technology Data Exchange (ETDEWEB)

    Atlas, R. [Louisville Univ., Louisville, KY (United States); Bragg, J. [Creative Petroleum Solutions, Houston, TX (United States)

    2007-07-01

    Shoreline samples from the Exxon Valdez oil spill were used to study the limitations and strengths of different conserved components as markers based on a 17-year field monitoring program. Approximately 100 oil samples collected from the shoreline in Prince William Sound, Alaska from 1999-2006 had been analyzed for internal markers such as chrysenes, terpanes, steranes and triaromatic steroids and then used to assess the biodegradation of the spilled petroleum. The specific biomarkers used in this study were selected to exclude those that might be generated via biodegradation and were chosen from those having the most significant concentrations in the extracts. Concentrations of the recovered weathered oil compounds were quantified and the concentrations of the polycyclic aromatic hydrocarbons (PAH) components were measured in the aromatic fractions. The extent of PAH weathering was subsequently calculated as a percentage loss of total PAH in order to calculate a bioremediation index to evaluate if an oil at a given shoreline may be amenable to bioremediation (or nutrient addition) to accelerate removal of remaining PAH. In order to compare the extent of weathering over the 17 years since the spill, chemical analyses were performed for samples from 1989-1991 for which no biomarkers were measured. The weathering of the oil has progressed in such a way that most of the remaining oil is now highly weathered. The trend of increasing biodegradation with time indicates that given sufficient time, the oil will continue to degrade naturally until all of the PAH components are consumed. The most stable biomarker compounds to quantify the loss of PAH or other oil components was shown to be C{sub 29}R-stigmastane. 35 refs., 4 tabs., 7 figs.

  2. Assessing the long-term weathering of petroleum on shorelines : uses of conserved components for calibrating loss and bioremediation potential, Volume 1

    Energy Technology Data Exchange (ETDEWEB)

    Atlas, R. [Louisville Univ., Louisville, KY (United States); Bragg, J. [Creative Petroleum Solutions, Houston, TX (United States)

    2007-07-01

    Shoreline samples from the Exxon Valdez oil spill were used to study the limitations and strengths of different conserved components as markers based on a 17-year field monitoring program. Approximately 100 oil samples collected from the shoreline in Prince William Sound, Alaska from 1999-2006 had been analyzed for internal markers such as chrysenes, terpanes, steranes and triaromatic steroids and then used to assess the biodegradation of the spilled petroleum. The specific biomarkers used in this study were selected to exclude those that might be generated via biodegradation and were chosen from those having the most significant concentrations in the extracts. Concentrations of the recovered weathered oil compounds were quantified and the concentrations of the polycyclic aromatic hydrocarbons (PAH) components were measured in the aromatic fractions. The extent of PAH weathering was subsequently calculated as a percentage loss of total PAH in order to calculate a bioremediation index to evaluate if an oil at a given shoreline may be amenable to bioremediation (or nutrient addition) to accelerate removal of remaining PAH. In order to compare the extent of weathering over the 17 years since the spill, chemical analyses were performed for samples from 1989-1991 for which no biomarkers were measured. The weathering of the oil has progressed in such a way that most of the remaining oil is now highly weathered. The trend of increasing biodegradation with time indicates that given sufficient time, the oil will continue to degrade naturally until all of the PAH components are consumed. The most stable biomarker compounds to quantify the loss of PAH or other oil components was shown to be C{sub 29}R-stigmastane. 35 refs., 4 tabs., 7 figs.

  3. UVB in solar-simulated light causes formation of BaP-photoproducts capable of generating phosphorylated histone H2AX.

    Science.gov (United States)

    Ohnuki, Go; Toyooka, Tatsushi; Ibuki, Yuko

    2010-09-30

    Polycyclic aromatic hydrocarbons (PAHs), wide-spread mutagenic and carcinogenic environmental pollutants, are consistently exposed to sunlight in the environment. Our previous paper showed that benzo[a]pyrene (BaP) exposed to solar-simulated light (SSL) induced phosphorylation of histone H2AX (γ-H2AX) [T. Toyooka, G. Ohnuki, Y. Ibuki, Solar-simulated light-exposed benzo[a]pyrene induces phosphorylation of histone H2AX, Mutat. Res. 650 (2008) 132-139], a marker of DNA double strand breaks. In this study, we found the ultraviolet B (UVB) region of SSL to produce photomodified BaP with high cytotoxicity and the ability to generate γ-H2AX. Degradation of BaP by SSL, resulting in an increase in cytotoxicity and the generation of γ-H2AX, was decreased by UVB-masking using a glass plate. Exposure to UVB itself increased the cytotoxicity of BaP and amount of γ-H2AX generated. Other PAHs, 1,2-benzoanthracene and 1,2:5,6-dibenzoanthracene, which absorb UVB, also showed enhanced cytotoxicity and the promoted the generation of γ-H2AX after exposure to SSL, whereas naphthalene and chrysene, which have low absorption in the UVB region, did not. These findings suggested that UVB is important for the degradation of PAHs having absorbance in this region, but that the production of genotoxic intermediates during the degradation process needs to be considered. UVB is a two-edged blade in environments, effectively degrading toxic chemicals but also producing genotoxic compounds as reactive intermediates.

  4. Emission characteristics of polycyclic aromatic hydrocarbons from combustion of different residential coals in North China

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Wen X. [Laboratory for Earth Surface Processes, College of Urban and Environmental Sciences, Peking University, Beijing 100871 (China)], E-mail: wxliu@urban.pku.edu.cn; Dou Han; Wei, Zhi C.; Chang Biao; Qiu, Wei X.; Liu Yuan; Tao Shu [Laboratory for Earth Surface Processes, College of Urban and Environmental Sciences, Peking University, Beijing 100871 (China)

    2009-02-01

    Emission properties of polycyclic aromatic hydrocarbons (PAHs) from combustion of six residential coals in North China were investigated. The results indicated that, the total emission factors (EFs) for 15 PAH species in gaseous and particulate phases ranged from 52.8 to 1434.8 mg/kg with a decreasing sequence of local bituminous coals and anthracite coals, and honeycomb briquettes were largely dependent on the raw coals used to produce them. Particulate phase, dominated by median or high molecular weight components, made a major contribution (68.8% - 76.5%) to the total EFs for bituminous coals, while gaseous phase with principal low molecular weight species accounted for most (86.3% - 97.9%) of the total EFs for anthracite coals. The phase partitioning of PAH emission for honeycomb briquettes was similarly dependent on the crude coals. The total EFs, phase partitioning and component profiles of emitted PAHs were mainly influenced by the inner components of the studied coals. Burning mode and flue number on household coal-stoves also affected the emission characteristics by means of the oxygen supply. A sum of seven carcinogenic PAHs, benzo(a)pyrene(BaP)-equivalent carcinogenic power and total toxicity potency expressed in 2,3,7,8-tetrachlorodibenzo-dioxin(TCDD) toxic equivalence exhibited that bituminous coals and produced honeycomb briquettes had remarkably elevated values. Fluoranthene, benzo(b)fluoranthene, benzo(k)fluoranthene, chrysene and indeno(1,2,3-cd)pyrene from anthracite coals showed higher levels of BaP-based toxic equivalent factor, though the other toxicity indices were rather low for this type of coal.

  5. Water quality, organic chemistry of sediment, and biological conditions of streams near an abandoned wood-preserving plant site at Jackson, Tennessee

    Science.gov (United States)

    Bradfield, A.D.; Flexner, N.M.; Webster, D.A.

    1993-01-01

    An investigation of water quality, organic sediment chemistry, and biological conditions of streams near an abandoned wood-preserving plant site at Jackson, Tennessee, was conducted during December 1990. The study was designed to assess the extent of possible contamination of water and biota in the streams from creosote-related discharge originating at this Superfund site. Central Creek, adjacent to the plant, had degraded water quality and biological conditions. Water samples from the most downstream station on Central Creek contained 30 micrograms per liter of pentachlorophenol, which exceeds the State's criterion maximum concentrations of 9 micrograms per liter for fish and aquatic life. Bottom-sediment samples from stations on Central Creek contained concentrations of acenaphthene, napthalene, and phenanthrene ranging from 1,400 to 2,500 micrograms per kilogram. Chronic or acute toxicity resulted during laboratory experiments using test organisms exposed to creosote-related contaminants. Sediment elutriate samples from Central Creek caused slightly to highly toxic effects on Ceriodaphnia dubia. Pimephales promelas, and Photobacterium phosphoreum. Fish-tissue samples from this station contained concentrations of naphthalene. dibenzofuran, fluorene, and phenanthrene ranging from 1.5 to 3.9 micrograms per kilogram Blue-green algae at this station represented about 79 percent of the organisms counted, whereas diatoms accounted for only 11 percent. Benthic invertebrate and fish samples from Central Creek had low diversity and density. Sediment samples from a station on the South Fork Forked Deer River downstream from its confluence with Central Creek contained concentrations of acenaphthene, anthracene, chrysene, fluoranthene, fluorene, pyrere, and phenanthrene ranging from 2,800 to 69,000 micrograms per kilogram. Sediment elutriate samples using water as elutriate from this station contained concentrations of extractable organic compounds ranging from an estimated

  6. Atmospheric behaviors of polycyclic aromatic hydrocarbons at a Japanese remote background site, Noto peninsula, from 2004 to 2014

    Science.gov (United States)

    Tang, Ning; Hakamata, Mariko; Sato, Kousuke; Okada, Yumi; Yang, Xiaoyang; Tatematsu, Michiya; Toriba, Akira; Kameda, Takayuki; Hayakawa, Kazuichi

    2015-11-01

    Total suspended particulates were collected at a Japanese remote background site (Noto Air Monitoring Station; NAMS) on the Noto Peninsula from September 2004 to June 2014. Nine polycyclic aromatic hydrocarbons (PAHs) in the particulates (fluoranthene, pyrene, benz[a]anthracene, chrysene, benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[a]pyrene, benzo[ghi]perylene and indeno[1,2,3-cd]pyrene) were determined by HPLC with fluorescence detection. The mean total concentrations of the nine PAHs in the cold season (November to May for the years 2004-2014) was 670 pg m-3 (range 37-4100 pg m-3). The mean total concentration in the warm season (June to October for the same period) was 170 pg m-3 (range 31-960 pg m-3). The atmospheric PAH level at NAMS decreased in recent years, although no significant change was found in the warm season. An analysis of meteorological conditions showed that the atmospheric PAHs at NAMS were long range transported from Northeast China in the cold seasons and were contributed to by Japanese domestic sources in the warm seasons. Lower concentration ratios of reactive PAHs to their isomers at NAMS also supported these results. Activities associated with the Beijing Olympic and Paralympic Games in 2008 and reconstruction after the 2007 Noto Hanto earthquake may have contributed to the yearly variations of atmospheric PAH levels at NAMS during the period 2007-2009. Source control measures implemented by the Chinese and Japanese governments appear to have been effective in decreasing the atmospheric PAH levels at NAMS in recent years.

  7. [Characterization of PAHs in fly ashes from coke production].

    Science.gov (United States)

    Mu, Ling; Peng, Lin; Liu, Xiao-Feng; Bai, Hui-Ling; Zhang, Jian-Qiang

    2013-03-01

    In order to investigate the characteristics of polycyclic aromatic hydrocarbons (PAHs) in ashes from coking, PAHs in ashes from three coke production plants were analyzed with GC-MS, and the distribution characteristics of PAHs and potential toxicity risk were discussed. The sum of 16 EPA prior PAHs varied from 8.17 x 10(2) to 5.17 x 10(3) microg x g(-1). PAH contents from the coke oven (stamp charging) with the height of 3.2 m were two times higher than those from the one (top charging) with the height of 6.0 m, and PAHs in ashes from coal charging were significantly higher than those from coke pushing in the same plant. Four-ring and five-ring PAHs were the dominant species in ashes from coking and the sum of them accounted for more than 80.00% of total PAHs. Chrysene (Chr), benzo [a] anthracene (BaA) and benzo [b] fluoranthene (BbF) were abundant in all ash samples. The content of total BaP-based toxic equivalency (BaPeq) ranged from 1.64 x 10(2) to 9.57 x 10(2) microg x g(-1). From the carcinogenic point of view, besides benzo [a] pyrene (BaP), dibenz [a,h] anthracene (DbA) contributed most to the overall toxicity of PAHs, followed by BaA and BbF. BaPeq concentration from coal charging was 5.21-fold higher than that from coke pushing, indicating that different reuse ways should be considered based on their specific toxicity profiles of PAHs. PMID:23745428

  8. Airborne exposures to PAH and PM2.5 particles for road paving workers applying conventional asphalt and crumb rubber modified asphalt.

    Science.gov (United States)

    Watts, R R; Wallingford, K M; Williams, R W; House, D E; Lewtas, J

    1998-01-01

    Personal exposure monitoring was conducted for road paving workers in three states. A research objective was to characterize and compare occupational exposures to fine respirable particles (asphalt and asphalt containing crumb rubber from shredded tires. Workers not exposed to asphalt fume were also included for comparison (to support the biomarker component of this study). The rubber content of the crumb rubber modified (CRM) asphalt at the three study sites was 12, 15, and 20%. A comparison of some specific job categories from two sites indicates greater potential carcinogenic PAH exposures during CRM asphalt work, however, the site with the greatest overall exposures did not indicate any differences for specific jobs. A statistical analysis of means for fine particle, pyrene and total carcinogenic PAH personal exposure shows, with two exceptions, there were no differences in exposures for these three measurement variables. One site shows significantly elevated pyrene exposure for CRM asphalt workers and another site similarly shows greater carcinogenic PAH exposure for CRM asphalt workers. Conventional and CRM asphalt worker airborne exposures to the PAH carcinogen marker, BaP, were very low with concentrations comparable to ambient air in many cities. However, this study demonstrates that asphalt road paving workers are exposed to elevated airborne concentrations of a group of unknown compounds that likely consist of the carcinogenic PAHs benz(a)anthracene, chrysene and methylated derivatives of both. The research described in this article has been reviewed in accordance with U.S. Environmental Protection Agency policy and approved for publication. Mention of trade names or commercial products does not constitute endorsement or recommendation for use. PMID:9577752

  9. Occurrence of gaseous and particulate polycyclic aromatic hydrocarbons in the urban atmosphere: study of sources and ambient temperature effect on the gas/particle concentration and distribution

    Energy Technology Data Exchange (ETDEWEB)

    Tsapakis, Manolis [Environmental Chemical Processes Laboratory (ECPL), Department of Chemistry, University of Crete, EL-71409 Heraklion (Greece); Stephanou, Euripides G. [Environmental Chemical Processes Laboratory (ECPL), Department of Chemistry, University of Crete, EL-71409 Heraklion (Greece)]. E-mail: stephanou@chemistry.uoc.gr

    2005-01-01

    The presence of polycyclic aromatic hydrocarbons (PAHs) in an urban region (Heraklion, Greece) and processes that govern their atmospheric fate were studied from November 2000 until February 2002. Sixteen samples were collected, by using an artifact-free sampling device, on a monthly basis and the concentration of PAHs in gas and particulate phase was determined. The most abundant members (gas + particles) were phenanthrene (20.0 {+-} 7.0 ng m{sup -3}), fluoranthene (6.5 {+-} 1.7 ng m{sup -3}), pyrene (6.6 {+-} 2.4 ng m{sup -3}), and chrysene (3.1 {+-} 1.5 ng m{sup -3}). Total concentration (gas + particulate) of PAH ranged from 44.3 to 129.2 ng m{sup -3}, with a mean concentration of 79.3 ng m{sup -3}. Total concentration of PAHs in gas phase ranged from 31.4 to 84.7 ng m{sup -3} with non-observable seasonal variation. Conversely, maximum PAH concentrations in the particulate phase occurred during winter months. Particulate concentration varied from 11.4 to 44.9 ng m{sup -3}, with an average of 25.2 ng m{sup -3}. PAH distribution between gas and particulate phase was in agreement with the sub-cooled vapor pressure. Shift in gas/particle distribution due to difference in ambient temperature elucidated to some extent the seasonal variation of the concentration of PAHs in particles. - Capsule: Ambient PAH partitioning between gas and particle phases vary between compounds and with environmental conditions.

  10. Substrate Bioaugmentation of Waste Engine Oil Polluted Soil

    Directory of Open Access Journals (Sweden)

    Beckley Ikhajiagbe

    2012-01-01

    Full Text Available The present study investigated the impact of substrate microbial augmentation on the bioremediation of Waste Engine Oil (WEO polluted soil. Five different concentrations of WEO in soil on weight basis were obtained by thoroughly mixing WEO in measured soil: 1.0, 2.5, 5.0 and 10.0% w/w. The unpolluted soil was used as the control (0% w/w experiment. The set up was left for 5 months without physically disturbing the soil. After 5 months, the soils were first amended with sawdust and then inoculated with mycelia of Pleurotus tuberregium. Significant (p = 0.05 decreases in soil physicochemical parameters were recorded 9 months after bioaugmentation (9 MAB, excepting total organic carbon and total nitrogen, which showed significant increases throughout the experiment period. Total (100% remediation of some PAH compounds - benzo(aanthracene, benzo(apyrene, benzo(bfluoranthene, benzo(g,h,iperylene, benzo(kfluoranthene, chrysene, dibenzo(a,hanthracene, fluoranthene, fluorene, and indeno(1,2,3-c,dpyrene - was recorded. Over sixty per cent (66.22% of total individual PAH compounds were completely (100% remediated. Achromobacter sp., Clostridium sp., Sarcina sp., Micrococcus sp., Nocardia sp., Penicillium sp., Rhizopus stolonifer, Mucor sp., Trichoderma sp., Aspergillus niger, A. fumigatus, A. flavus and Geotrichum sp. were dominant microorganism species in the WEO polluted soil. Significant decreases in heavy metal concentration resulted in significant reductions in Environmental Risk Factor (ERF, which implied less possibility for ecological risk for heavy metal constituents. ERF presupposes that Pb (ERF range, -69.30 to -14.97 and V (ERF range, -0.01 to 0.86 were significant potential ecological threats at 5MAP, but at 9 MAB, ERF value had decreased, with ERF ranges for Pb and V being 5.64 to 32.64 and 1.70 to 1.83, respectively.

  11. Tracing biogeochemical and microbial variability over a complete oil sand mining and recultivation process.

    Science.gov (United States)

    Noah, Mareike; Lappé, Michael; Schneider, Beate; Vieth-Hillebrand, Andrea; Wilkes, Heinz; Kallmeyer, Jens

    2014-11-15

    Recultivation of disturbed oil sand mining areas is an issue of increasing importance. Nevertheless only little is known about the fate of organic matter, cell abundances and microbial community structures during oil sand processing, tailings management and initial soil development on reclamation sites. Thus the focus of this work is on biogeochemical changes of mined oil sands through the entire process chain until its use as substratum for newly developing soils on reclamation sites. Therefore, oil sand, mature fine tailings (MFTs) from tailings ponds and drying cells and tailings sand covered with peat-mineral mix (PMM) as part of land reclamation were analyzed. The sample set was selected to address the question whether changes in the above-mentioned biogeochemical parameters can be related to oil sand processing or biological processes and how these changes influence microbial activities and soil development. GC-MS analyses of oil-derived biomarkers reveal that these compounds remain unaffected by oil sand processing and biological activity. In contrast, changes in polycyclic aromatic hydrocarbon (PAH) abundance and pattern can be observed along the process chain. Especially naphthalenes, phenanthrenes and chrysenes are altered or absent on reclamation sites. Furthermore, root-bearing horizons on reclamation sites exhibit cell abundances at least ten times higher (10(8) to 10(9) cells g(-1)) than in oil sand and MFT samples (10(7) cells g(-1)) and show a higher diversity in their microbial community structure. Nitrate in the pore water and roots derived from the PMM seem to be the most important stimulants for microbial growth. The combined data show that the observed compositional changes are mostly related to biological activity and the addition of exogenous organic components (PMM), whereas oil extraction, tailings dewatering and compaction do not have significant influences on the evaluated compounds. Microbial community composition remains relatively

  12. Evolution of organic molecules under Mars-like UV radiation with EXPOSE-R2, a photochemistry experiment outside the International Space Station

    Science.gov (United States)

    Rouquette, Laura; Stalport, Fabien; Cottin, Hervé; Coll, Patrice; Szopa, Cyril; Saiagh, Kafila; Poch, Olivier; Khalaf, Diana; Chaput, Didier; Grira, Katia; Chaouche, Naila; Dequaire, Tristan

    2016-10-01

    The detection and identification of organic molecules on Mars are of prime importance, as some of these molecules are life precursors and components. While in situ planetary missions are searching for them, it is essential to understand how organic molecules evolve and are preserved at the surface of Mars. Indeed the harsh conditions of the environment of Mars such as ultraviolet (UV) radiation or oxidative processes could explain the low abundance and diversity of organic molecules detected by now.The EXPOSE R2 facility has been placed in low Earth orbit (LEO) under solar radiation, outside the International Space Station (ISS) in 2014. One of the EXPOSE R2 experiment, called PSS (Photochemistry on the Space Station), is dedicated to astrobiology- and astrochemistry-related studies. Part of PSS samples have been dedicated to the study of the evolution of organic molecules under Mars-like surface radiation conditions. Indeed, UV radiation above 200 nm reaches the surface of Mars and could degrade organic matter. Organic samples have been exposed directly to the Sun under KBr filters (>200 nm) from November 2014 to February 2016, mimicking the UV radiation conditions of the surface of Mars. Four types of samples were exposed as thin layers of solid molecules: adenine, adenine with nontronite (a kind of clay mineral detected on Mars), chrysene and glycine with nontronite.To characterize the evolution of our samples under irradiation, infrared (IR) transmission analyses were performed, before the launch of EXPOSE R2 to the ISS in 2014, and after the exposure in space and the return on Earth, this year. These analyses allowed determining whether each molecule is preserved or photodegraded, and if so, its photolysis rate. The effect of nontronite on organic molecules preservation has been investigated as well. We also compared these results from LEO with laboratory data, obtained by irradiating organic samples under a UV lamp.

  13. Characterization of polycyclic aromatic hydrocarbon emissions in the particulate phase from burning incenses with various atomic hydrogen/carbon ratios

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Tzu-Ting, E-mail: d89844001@ntu.edu.tw [Department of Environmental Engineering and Health, Yuanpei University, No. 306, Yuanpei St., Hsin Chu, 300, Taiwan (China); Lin, Shaw-Tao [Department of Applied Chemistry, Providence University, 200 Chung-Chi Rd., Salu Dist., Taichung City 43301, Taiwan (China); Lin, Tser-Sheng [Department of Safety, Health, and Environmental Engineering, National United University, 2 Lien Da, Maioli, 360, Taiwan (China); Hong, Wei-Lun [Department of Environmental Engineering and Health, Yuanpei University, No. 306, Yuanpei St., Hsin Chu, 300, Taiwan (China)

    2012-01-01

    Polycyclic aromatic hydrocarbons in the particulate phase generated from burning various incense was investigated by a gas chromatography/mass spectrometry. Among the used incenses, the atomic H/C ratio ranged from 0.51 to 1.69, yielding the emission factor ranges for total particulate mass and PAHs of 4.19-82.16 mg/g and 1.20-9.50 {mu}g/g, respectively. The atomic H/C ratio of the incense was the key factor affecting particulate mass and the PAHs emission factors. Both the maximum emission factor and the slowest burning rate appear at the H/C ratio of 1.57. The concentrations of the four-ring PAHs predominated and the major species among the 16 PAHs were fluoranthene, phenanthrene, pyrene, and chrysene for most incense types. The benzo[a]pyrene, benzo[a]anthracene, benzo[b]fluoranthene, and dibenzo[a,h]anthracene accounted for 87.08-93.47% of the total toxic equivalency emission factor. - Highlights: Black-Right-Pointing-Pointer The atomic H/C ratio of incense was the key factor affecting PAHs emission factors. Black-Right-Pointing-Pointer Burning incense with lower atomic H/C ratio minimized the production of total PAHs. Black-Right-Pointing-Pointer The BaP, BaA, BbF, and DBA accounted for 87.08-93.47% of the TEQ emission factor. Black-Right-Pointing-Pointer Special PAH ratios were regarded as characteristic ratios for burning incense.

  14. Oils from different depth in the Alagoas sub-basin distribution and concentration; Oleos em diferentes profundidades na sub-bacia Alagoas: distribuicao e econcentracao

    Energy Technology Data Exchange (ETDEWEB)

    Reboucas, Lucia M.C.; Sant' Ana, Antonio E.G.; Sabino, Adilson R.; Nogueira, Fred A.R.; Moraes, Reinaldo J.R.; Crispim, Alessandre [Universidade Federal de Alagoas (UFAL), Maceio, AL (Brazil). Inst. de Quimica e Biotecnologia . Lab. de Analises de Biomarcadores e Semioquimicos]. E-mail: lmcr@qui.ufal.br

    2008-07-01

    This paper reports the distribution and the concentration of n-alkane homologue series and the HPA compounds in 22 oils from Alagoas sub-basin, Pilar Field, Brazil. The n-alkane profile of whole oil gas chromatograms (CG-FID) to light, medium and heave oils represented no-biodegraded oils. The light and medium oils have n-alkane distribution with a maximum in nC{sub 10} and nC{sub 17}. The ration pristine/phytane (P/F) between 1,5 and 2,7 suggest Lacustrine origin. The nalkane distribution from the heavy oils show two maximum between nC{sub 15} and nC{sub 23}. The concentrations of n-alkane are different to all the 22 oils. The F2 fraction classified as light (API>39), medium (36chrysene, mono- and triaromatic steroid, benzohopane and their alkyl derivates, were identified in the oils. (author)

  15. Single-laboratory validation of a saponification method for the determination of four polycyclic aromatic hydrocarbons in edible oils by HPLC-fluorescence detection.

    Science.gov (United States)

    Akdoğan, Abdullah; Buttinger, Gerhard; Wenzl, Thomas

    2016-01-01

    An analytical method is reported for the determination of four polycyclic aromatic hydrocarbons (benzo[a]pyrene (BaP), benz[a]anthracene (BaA), benzo[b]fluoranthene (BbF) and chrysene (CHR)) in edible oils (sesame, maize, sunflower and olive oil) by high-performance liquid chromatography. Sample preparation is based on three steps including saponification, liquid-liquid partitioning and, finally, clean-up by solid phase extraction on 2 g of silica. Guidance on single-laboratory validation of the proposed analysis method was taken from the second edition of the Eurachem guide on method validation. The lower level of the working range of the method was determined by the limits of quantification of the individual analytes, and the upper level was equal to 5.0 µg kg(-1). The limits of detection and quantification of the four PAHs ranged from 0.06 to 0.12 µg kg(-1) and from 0.13 to 0.24 µg kg(-1). Recoveries of more than 84.8% were achieved for all four PAHs at two concentration levels (2.5 and 5.0 µg kg(-1)), and expanded relative measurement uncertainties were below 20%. The performance of the validated method was in all aspects compliant with provisions set in European Union legislation for the performance of analytical methods employed in the official control of food. The applicability of the method to routine samples was evaluated based on a limited number of commercial edible oil samples.

  16. 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

  17. Panel study on indoor exposure to polyaromatic hydrocarbons in relation to DNA damage biomarkers

    Directory of Open Access Journals (Sweden)

    Gudrun Koppen

    2015-06-01

    Naphthalene - a possible carcinogenic (IARC group 2B compound - was in both seasons relatively the most important PAH in indoor air (70-80%. More heavy carcinogenic PAHs (c-PAHs were – mainly in summer – hard to detect. In house dust mainly the 3 and 4-ring phenanthrene, fluorene, pyrene and the 4- and 5-ring structures chrysene and benzo[b]fluoranthene made the most important contribution to the EPA-PAH mixture. All PAH fractions in house dust were highest in winter time. DNA breaks in MWBC - but not of the whole white blood cells fraction - of the inhabitants were strongly associated with air as wells as house dust v-PAHs and c-PAHs, i.e. between 13 to 25% increase in number of breaks for doubling of the indoor PAH concentration. The indoor air v-PAHs were also associated with oxidative damage measured in whole blood and urine, respectively via the FPG comet assay and 8-oxodG. In the same way, also oxidized sites in whole blood, but not in MWBC correlated with NO2, PM10 and O3 concentrations 7 days before blood collection. Aside from lymphocytes and monocytes, which are present in the MWBC - and have a half-life of weeks to months - whole blood also contains a considerable amount of granulocytes, which have a rather short half-life of some days. In conclusion: DNA damage in isolated MWBC and the whole white blood cell fraction reflected the inhabitants’ exposure to indoor PAHs, although with different sensitivity.

  18. Considerations for risk-based corrective action at contaminated gas works sites: examples from Canada and the United Kingdom

    Energy Technology Data Exchange (ETDEWEB)

    Hardisty, P.E.; Sevigny, J.H.; Croft, R.C.; Bracken, R.A.; Hobby, R. [Komex Clarke Bond, Bristol (United Kingdom)

    1995-12-31

    Risk-based corrective action programmes for contaminated gas works sites focus on organic and inorganic compounds posing potential health effects to humans and/or ecological receptors. These programmes include an understanding of the nature and extent of contamination, transport and fate in appropriate pathways, toxicological effects to human health and the environment, and remedial options. Potential risk-generating substances at gas works sites in the United Kingdom and Canada include coal tar and tar residues, spent oxides, sulphur compounds, and heavy metals. Organic compounds found in coal tar can include monocyclic (e.g. benzene, phenols) and polycyclic (e.g. naphthalene, chrysene) aromatic hydrocarbons. Tar and some of its components are carcinogenic. Metals and sulphur may be present at gas works sites. Sulphur contaminated soils can have depressed pH, which can lead to metals mobilization, and contaminated groundwater. Metals can be of concern in soils and groundwater, as can spent oxides from town gas manufacturing. These may include varying proportions of cyanide, either as relatively immobile complexed ferro-ferric cyanide (i.e. blue billy), or as more mobile and toxic free cyanide. Aquifers and surface water bodies can be pathways for dissolved metals or organic compounds with elevated aqueous solubilities. Some components of coal tar have appreciable vapour pressures and may emit odours if in near-surface soils, pathways exist via dermal contact or ingestion. Case histories from two coal gasification sites, one in the UK and one in Canada, are presented and discussed. 3 refs., 1 tab.

  19. New observations on PAH pollution in old heavy industry cities in northeastern China

    International Nuclear Information System (INIS)

    This study investigated the distinctive PAHs adsorbed on street dust near various industries in the three typical industrialized cities of Daqing (DQ), Harbin (HEB) and Jilin (JL) in northeastern China. The mean ∑PAHs concentrations in street dust of DQ, HEB and JL were 1.84, 4.87, 12.38 μg/g, respectively. Typical petroleum resource city DQ had higher proportions of low and medium ringed PAHs with higher proportions of phenanthrene (Phe), naphthalene (Nap), fluoranthene (Flua) and chrysene (Chr) at industrial sites. Typical chemical processing city JL had higher proportions of medium and high ringed PAHs with higher proportions of Flua, benz[a]anthracene (BaA), pyrene (Pyr) and benzo[a]pyrene (BaP) at industrial sites. Phe, Flua, Pyr and Chr were four major PAHs from most studied industries. The distinctive PAH emissions from the ferroalloy plant were BaA and BaP. BaA and BaP concentrations decreased by 90% at sites more than 2 km away from the ferroalloy plant. - Highlights: • Industry types determined PAH pollution characteristics at industrial sites. • Petroleum resource city Daqing had more low and medium ringed PAHs. • Phe, Flua, Pyr and Chr were major PAHs at most studied industrial sites. • The distinctive PAH emissions from the ferroalloy plant were BaA and BaP. • The major industry pollution impact radius was found to be about 2 km. - This paper investigated the signature of PAH contamination in street dust from 3 cities with contrasting industries

  20. 3,3'-Diindolylmethane induces G1 arrest and apoptosis in human acute T-cell lymphoblastic leukemia cells.

    Directory of Open Access Journals (Sweden)

    Lyndsey E Shorey

    Full Text Available Certain bioactive food components, including indole-3-carbinol (I3C and 3,3'-diindolylmethane (DIM from cruciferous vegetables, have been shown to target cellular pathways regulating carcinogenesis. Previously, our laboratory showed that dietary I3C is an effective transplacental chemopreventive agent in a dibenzo[def,p]chrysene (DBC-dependent model of murine T-cell lymphoblastic lymphoma. The primary objective of the present study was to extend our chemoprevention studies in mice to an analogous human neoplasm in cell culture. Therefore, we tested the hypothesis that I3C or DIM may be chemotherapeutic in human T-cell acute lymphoblastic leukemia (T-ALL cells. Treatment of the T-ALL cell lines CCRF-CEM, CCRF-HSB2, SUP-T1 and Jurkat with DIM in vitro significantly reduced cell proliferation and viability at concentrations 8- to 25-fold lower than the parent compound I3C. DIM (7.5 µM arrested CEM and HSB2 cells at the G(1 phase of the cell cycle and 15 µM DIM significantly increased the percentage of apoptotic cells in all T-ALL lines. In CEM cells, DIM reduced protein expression of cyclin dependent kinases 4 and 6 (CDK4, CDK6 and D-type cyclin 3 (CCND3; DIM also significantly altered expression of eight transcripts related to human apoptosis (BCL2L10, CD40LG, HRK, TNF, TNFRSF1A, TNFRSF25, TNFSF8, TRAF4. Similar anticancer effects of DIM were observed in vivo. Dietary exposure to 100 ppm DIM significantly decreased the rate of growth of human CEM xenografts in immunodeficient SCID mice, reduced final tumor size by 44% and increased the apoptotic index compared to control-fed mice. Taken together, our results demonstrate a potential for therapeutic application of DIM in T-ALL.

  1. Mass spectrometric analysis with cluster projectiles and coincidence counting

    Energy Technology Data Exchange (ETDEWEB)

    Cox, B.D.

    1992-01-01

    Methods for maximizing the amount of secondary ion information, per primary projectile, are described. The method is based on time-of-flight mass spectrometry and event-by-event coincidence counting. The information obtained from coincidence counting time-of-flight mass spectrometry includes: (a) surface composition, (b) relative concentrations, and (c) degree of intermolecular mixing. The technique was applied to the study of an important new class of polymers: polymer blends. Secondary ion mass spectrometry, when applied to the analysis of synthetic polymers, induces backbone fragmentation which is characteristic of the homopolymer. The characteristic fingerprint peaks from polystyrene and poly(vinyl methyl ether) were used to identify the presence of these two polymers in a polymer blend. The percent coincidence between the characteristic secondary ions from each component of the blend were used to determine both the relative concentration and the degree of molecular mixing. Results indicate molecular segregation of the two polymers on the film surface. The largest degree of segregation was determined for the phase separated blends. The performance of this technique depends on the desorption efficiency of the primary projectiles. In practice one seeks primary ions which are surface sensitive, have controllable parameters such as size, velocity, and charge state, and generate high secondary ion yields. Focus was placed on the use of keV organic cluster projectiles to meet these criteria. Of interest to this study were C[sub 18] (chrysene), C[sub 24] (coronene), and C[sub 60] (buckminster-fulleren). Results indicate enhanced secondary ion yields for C[sub 60]. For example, when CsI is bombarded with 30 keV C[sub 60], the yields for I[sup [minus

  2. Polycyclic aromatic hydrocarbons in urban street dust and surface soil: comparisons of concentration, profile, and source.

    Science.gov (United States)

    Wang, De-Gao; Yang, Meng; Jia, Hong-Liang; Zhou, Lei; Li, Yi-Fan

    2009-02-01

    Street dust and surface soil samples in urban areas of Dalian, a coastal city in Liaoning Province, China, were collected and analyzed for 25 polycyclic aromatic hydrocarbons (PAHs). The concentrations, distribution, and sources of PAHs in dust and soil were determined. The concentrations of total PAHs in street dust ranged between 1890 and 17,070 ng/g (dry weight), with an average of 7460 ng/g, whereas the concentrations of total PAHs in surface soil varied greatly, from 650 to 28,900 ng/g, with a mean value of 6440 ng/g. Statistical paired t-test confirmed that total PAH concentrations have no significant difference between street dust and surface soil. Mean PAH concentrations in two type samples were much higher at industrial sites than at business/residential or garden sites. PAHs were dominated by higher molecular weight PAH (4- to 6-ring) homologues, which accounted for about 73% and 72% of total PAHs in street dust and surface soil, respectively. Principal component analysis was used in source apportionment of PAHs in dust and soil. Pyrogenic and petrogenic sources contributed 70% and 22.4% of total PAHs in street dusts, and fossil fuel (coal and petroleum) and biomass combustion accounted for 64.4% and 5.6% of total PAHs in pyrogenic sources, respectively. In surface soil, total PAHs were dominated by pyrogenic sources. The diagnostic ratios of benz[a]anthracene/chrysene confirmed that PAHs in street dust and surface soil of a Dalian urban zone might come mostly from the emission of local sources.

  3. Analysis of polycyclic aromatic hydrocarbons in street soil dust in Kumasi Metropolis of Ghana.

    Science.gov (United States)

    Essumang, D K; Dodoo, D K; Obiri, S; Oduro, A K

    2006-10-01

    Concentrations of polycyclic aromatic hydrocarbons (PAHs) in street soil dust from streets in Kumasi Metropolis in the Ashanti Region of the Republic of Ghana have been measured in this study. The concentrations of the various types of PAHs identified in this study are as follows: Naphthalene (m/e 128) - 41,700 microg/kg, Acenaphthylene (m/e 152) - 99,300 microg/kg, Acenaphthene (m/e 154) - 111,200 microg/kg, Fluorene (m/e 166) - 8,900 microg/kg, Carbazole (m/e 167) - 3,500 microg/kg, phenathrene (m/e 178) - 12,900 microg/kg, Anthracene (m/e 178) - 5,400 microg/kg, Fluoranthene (m/e 202) - 16,200 microg/kg, Pyrene (m/e 202) - 15,000 microg/kg, Benzo[a]anthracene (m/e 228) - 13,800 microg/kg, Chrysene (m/e 228) - 33,600 microg/kg, Benzo[k]fluoranthene (m/e 252) - 45,700 microg/kg, Benzo[a]pyrene (m/e 252) - 27,900 microg/kg, Perylene (m/e 252) - 57,200 microg/kg and Benzo[g, h, i]perylene (m/e 276) - 47,000 microg/kg. The results of the study shows that road users, like resident living in buildings within these areas, those engaged in commercial activities like hawking, and the general public are at risk of exposure to the toxic effects of the various types of PAHs from the exhaust of vehicles into the environment. According to these results, there is the potential for exposure to high levels of PAHs for road users and those living in urban environments or along highways.

  4. Occurrence of polycyclic aromatic hydrocarbons (PAHs in beached plastic pellets from Mumbai coast, India

    Directory of Open Access Journals (Sweden)

    HB Jayasiri

    2014-06-01

    Full Text Available PAHs are a class of ubiquitous pollutants which consist of two or more fused benzene rings in various arrangements. A number of PAH compounds are known carcinogens and bioaccumulate and biomagnify. These compounds originate naturally as well as anthropogenically through oil spills, incineration of waste and combustion of fossil fuels and wood. The environmental consequence of Plastic pellets is the sorption organic pollutants on their surface from the sea surface microlayer (SML where the hydrophobic contaminants are known to be enriched. The plastic pellets were collected along the recent high tide line from four beaches of Mumbai coast bimonthly during May 2011 - March 2012. A total of 72 pools of plastic pellets were extracted, fractionated and analysed by Gas Chromatograph coupled to a mass spectrometer to evaluate the extent and sources of 16 PAHs. The mean ΣPAH concentration in pellets was 9202.30±114.89 ng g-1 with a wide range (35.4-46191.58 ng g-1. The concentration of fluorene was found to be the highest (1606.30±251.54 ng g-1 followed by anthracene, chrysene and phenanthrene. The ΣPAH concentration was significantly varied among months and there was no significant difference among sites at  p=0.05. The 2-3 aromatic ring compounds accounted for 60% of the total PAHs in pellets of Mumbai coast while 4 rings and 5-6 rings compounds accounted for 26 and 14%, respectively. The ratio of low and high molecular weight PAHs indicated that the contamination by petrogenic sources was predominant over the pyrogenic ones in plastic pellets suggesting oil pollution in coastal area of Mumbai.Keywords: plastic pellets, PAHs, Mumbai, sources

  5. Measurement and estimated health risks of semivolatile organic compounds (PCBs, PAHs, pesticides, and phthalates) in ambient air at the Hanford Site

    Energy Technology Data Exchange (ETDEWEB)

    Patton, G.W.; Cooper, A.T.; Blanton, M.L.; Lefkovitz, L.F.; Gilfoil, T.J.

    1997-09-01

    Air samples for polychlorinated biphenyls (PCBs), chlorinated pesticides, phthalate plasticizers, and polycyclic aromatic hydrocarbons (PAHs) were collected at three Hanford Site locations (300-Area South Gate, southeast of 200-East Area, and a background location near Rattlesnake Springs). Samples were collected using high-volume air samplers equipped with a glass fiber filter and polyurethane foam plug sampling train. Target compounds were extracted from the sampling trains and analyzed using capillary gas chromatography with either electron capture detection or mass selective detection. Twenty of the 28 PCB congeners analyzed were found above the detection limits, with 8 of the congeners accounting for over 80% of the average PCB concentrations. The average sum of all individual PCB congeners ranged from 500-740 pg/m{sup 3}, with little apparent difference between the sampling locations. Twenty of the 25 pesticides analyzed were found above the detection limits, with endosulfan I, endosulfan II, and methoxychlor having the highest average concentrations. With the exception of the endosulfans, all other average pesticide concentrations were below 100 pg/m{sup 3}. There was little apparent difference between the air concentrations of pesticides measured at each location. Sixteen of the 18 PAHs analyzed were found above the detection limit. Phenanthrene, fluoranthene, pyrene, fluorene, chrysene, benzo(b)fluoranthene, and naphthalene were the only PAHs with average concentrations above 100 pg/m{sup 3}. Overall, the 300 Area had higher average PAH concentrations compared to the 200-East Area and the background location at Rattlesnake Springs; however, the air concentrations at the 300-Area also are influenced by sources on the Hanford Site and from nearby communities.

  6. Assessing the long-term weathering of petroleum on shorelines : uses of conserved components for calibrating loss and bioremediation potential, Volume 1

    International Nuclear Information System (INIS)

    Shoreline samples from the Exxon Valdez oil spill were used to study the limitations and strengths of different conserved components as markers based on a 17-year field monitoring program. Approximately 100 oil samples collected from the shoreline in Prince William Sound, Alaska from 1999-2006 had been analyzed for internal markers such as chrysenes, terpanes, steranes and triaromatic steroids and then used to assess the biodegradation of the spilled petroleum. The specific biomarkers used in this study were selected to exclude those that might be generated via biodegradation and were chosen from those having the most significant concentrations in the extracts. Concentrations of the recovered weathered oil compounds were quantified and the concentrations of the polycyclic aromatic hydrocarbons (PAH) components were measured in the aromatic fractions. The extent of PAH weathering was subsequently calculated as a percentage loss of total PAH in order to calculate a bioremediation index to evaluate if an oil at a given shoreline may be amenable to bioremediation (or nutrient addition) to accelerate removal of remaining PAH. In order to compare the extent of weathering over the 17 years since the spill, chemical analyses were performed for samples from 1989-1991 for which no biomarkers were measured. The weathering of the oil has progressed in such a way that most of the remaining oil is now highly weathered. The trend of increasing biodegradation with time indicates that given sufficient time, the oil will continue to degrade naturally until all of the PAH components are consumed. The most stable biomarker compounds to quantify the loss of PAH or other oil components was shown to be C29R-stigmastane. 35 refs., 4 tabs., 7 figs

  7. Emulsification liquid-liquid microextraction based on deep eutectic solvent: An extraction method for the determination of benzene, toluene, ethylbenzene and seven polycyclic aromatic hydrocarbons from water samples.

    Science.gov (United States)

    Khezeli, Tahere; Daneshfar, Ali; Sahraei, Reza

    2015-12-18

    In this study, for the first time, a simple, inexpensive and sensitive method named emulsification liquid-liquid microextraction based on deep eutectic solvent (ELLME-DES) was used for the extraction of benzene, toluene, ethylbenzene (BTE) and seven polycyclic aromatic hydrocarbons (PAHs) from water samples. In a typical experiment, 100μL of DES (as water-miscible extraction solvent) was added to 1.5mL of sample solution containing target analytes. A homogeneous solution was formed immediately. Injection of 100μL of THF (as emulsifier agent) into homogeneous solution provided a turbid state. After extraction, phase separation (aqueous phase/DES rich phase) was performed by centrifugation. DES rich phase was withdrawn by a micro-syringe and submitted to isocratic reverse-phase HPLC with UV detection. Under optimum conditions obtained by response surface methodology (RSM) and desirability function (DF), the calibration graphs were linear in the concentration range from 10 to 200μg/L for benzene, 10-400μg/L for toluene, 1-400μg/L for ethylbenzene, biphenyl, chrysene and fluorene, and 0.1-400μg/L for anthracene, benzo[a]pyrene, phenanthrene and pyrene. The coefficients of determination (r(2)) and limits of detection were 0.9924-0.9997 and 0.02-6.8μg/L, respectively. This procedure was successfully applied to the determination of target analytes in spiked water samples. The relative mean recoveries ranged from 93.1 to 103.3%. PMID:26614169

  8. Mechanism-Based Classification of PAH Mixtures to Predict Carcinogenic Potential.

    Science.gov (United States)

    Tilton, Susan C; Siddens, Lisbeth K; Krueger, Sharon K; Larkin, Andrew J; Löhr, Christiane V; Williams, David E; Baird, William M; Waters, Katrina M

    2015-07-01

    We have previously shown that relative potency factors and DNA adduct measurements are inadequate for predicting carcinogenicity of certain polycyclic aromatic hydrocarbons (PAHs) and PAH mixtures, particularly those that function through alternate pathways or exhibit greater promotional activity compared to benzo[a]pyrene (BaP). Therefore, we developed a pathway-based approach for classification of tumor outcome after dermal exposure to PAH/mixtures. FVB/N mice were exposed to dibenzo[def,p]chrysene (DBC), BaP, or environmental PAH mixtures (Mix 1-3) following a 2-stage initiation/promotion skin tumor protocol. Resulting tumor incidence could be categorized by carcinogenic potency as DBC > BaP = Mix2 = Mix3 > Mix1 = Control, based on statistical significance. Gene expression profiles measured in skin of mice collected 12 h post-initiation were compared with tumor outcome for identification of short-term bioactivity profiles. A Bayesian integration model was utilized to identify biological pathways predictive of PAH carcinogenic potential during initiation. Integration of probability matrices from four enriched pathways (P < .05) for DNA damage, apoptosis, response to chemical stimulus, and interferon gamma signaling resulted in the highest classification accuracy with leave-one-out cross validation. This pathway-driven approach was successfully utilized to distinguish early regulatory events during initiation prognostic for tumor outcome and provides proof-of-concept for using short-term initiation studies to classify carcinogenic potential of environmental PAH mixtures. These data further provide a 'source-to-outcome' model that could be used to predict PAH interactions during tumorigenesis and provide an example of how mode-of-action-based risk assessment could be employed for environmental PAH mixtures. PMID:25908611

  9. HPLC Measurement of the DNA Oxidation Biomarker, 8-oxo-7,8-dihydro-2'-deoxyguanosine, in Cultured Cells and Animal Tissues.

    Science.gov (United States)

    Chepelev, Nikolai L; Kennedy, Dean A; Gagné, Remi; White, Taryn; Long, Alexandra S; Yauk, Carole L; White, Paul A

    2015-01-01

    Oxidative stress is associated with many physiological and pathological processes, as well as xenobiotic metabolism, leading to the oxidation of biomacromolecules, including DNA. Therefore, efficient detection of DNA oxidation is important for a variety of research disciplines, including medicine and toxicology. A common biomarker of oxidatively damaged DNA is 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxo-dGuo; often erroneously referred to as 8-hydroxy-2'-deoxyguanosine (8-OH-dGuo or 8-oxo-dG)). Several protocols for 8-oxo-dGuo measurement by high pressure liquid chromatography with electrochemical detection (HPLC-ED) have been described. However, these were mainly applied to purified DNA treated with pro-oxidants. In addition, due to methodological differences between laboratories, mainly due to differences in analytical equipment, the adoption of published methods for detection of 8-oxo-dGuo by HPLC-ED requires careful optimization by each laboratory. A comprehensive protocol, describing such an optimization process, is lacking. Here, a detailed protocol is described for the detection of 8-oxo-dGuo by HPLC-ED, in DNA from cultured cells or animal tissues. It illustrates how DNA sample preparation can be easily and rapidly optimized to minimize undesirable DNA oxidation that can occur during sample preparation. This protocol shows how to detect 8-oxo-dGuo in cultured human alveolar adenocarcinoma cells (i.e., A549 cells) treated with the oxidizing agent KBrO3, and from the spleen of mice exposed to the polycyclic aromatic hydrocarbon dibenzo(def,p)chrysene (DBC, formerly known as dibenzo(a,l)pyrene, DalP). Overall, this work illustrates how an HPLC-ED methodology can be readily optimized for the detection of 8-oxo-dGuo in biological samples. PMID:26273842

  10. Origin of polycyclic aromatic hydrocarbons in lake sediments of the Mackenzie Delta.

    Science.gov (United States)

    Headley, John V; Marsh, Philip; Akre, Christine J; Peru, Kerry M; Lesack, Lance

    2002-08-01

    The concentrations and distribution of polycyclic aromatic hydrocarbons (PAHs) were assessed in sediment cores from among 14 lakes from three regions comprising a transect across the central Mackenzie Delta. PAHs were consistently found in the lake sediments, with parent concentrations in the 20-200 ng/g range. Concentrations were generally independent of depth in the sediment cores and this pattern was similar among the 3 regions of the delta. Concentrations increased in a westerly direction among the regions. For some lakes, the concentration of PAHs decreased with decreasing flooding frequency, and decreasing sedimentation rates. For the latter, maximum concentrations occurred at shallower depths within the sediment cores as flooding frequency among the lakes decreased. The distributions of C0-C4 alkylated 2- and 3- ring PAHs were consistent with a petrogenic origin, while the corresponding distribution of 4-ring PAHs appears to be more consistent with a biogenic or pyrogenic origin. Based on relative contributions to the overall PAH budget, a petrogenic source appears to be dominant. However, the pyrene/fluoranthene ratio is more consistent with a source derived from peat. The alkylated PAH profiles are inconsistent with those in the Athabasca River system, and supports a previously published hypothesis that the contribution of PAHs from the Athabasca oil sands to the lower Mackenzie River is minimal. A double ratio plot of chrysene vs dibenzothiophene, diagnostic of weathering, suggests most weathering occurred before the sediments were deposited in the lakes, while a double ratio plot of dibenzothiophene vs phenanthrene suggests a common source of PAHs across the delta, despite differing water sources from east to west across the delta. PAH inputs to the delta appear to mirror sediment inputs documented in previous work, where high sediment input from the Mackenzie mainstem during high floods dominates the delta sediment influx and masks any influence of the

  11. Calculation of the thermodynamic properties at elevated temperatures and pressures of saturated and aromatic high molecular weight solid and liquid hydrocarbons in kerogen, bitumen, petroleum, and other organic matter of biogeochemical interest

    Energy Technology Data Exchange (ETDEWEB)

    Richard, L.; Helgeson, H.C. [Univ. of California, Berkeley, CA (United States). Dept. of Geology and Geophysics

    1998-12-01

    To supplement the relatively sparse set of calorimetric data available for the multitude of high molecular weight organic compounds of biogeochemical interest, group additivity algorithms have been developed to estimate heat capacity power function coefficients and the standard molal thermodynamic properties at 25 C and 1 bar of high molecular weight compounds in hydrocarbon source rocks and reservoirs, including crystalline and liquid isoprenoids, steroids, tricyclic diterpenoids, hopanoids, and polynuclear aromatic hydrocarbons. A total of ninety-six group contributions for each coefficient and property were generated from the thermodynamic properties of lower molecular weight reference species for which calorimetric data are available in the literature. These group contributions were then used to compute corresponding coefficients and properties for {approximately}360 representative solid and liquid high molecular weight compounds in kerogen, bitumen, and petroleum for which few or no experimental data are available. The coefficients and properties of these high molecular weight compounds are summarized in tables, together with those of the groups and reference species from which they were generated. The tabulated heat capacity power function coefficients and standard molal thermodynamic properties at 25 C and 1 bar include selected crystalline and liquid regular, irregular and highly branched isoprenoids, tricyclic diterpanes, 17{alpha}(H)- and 17{beta}(H)-hopanes, 5{alpha}(H),14{alpha}(H)-, 5{beta}(H),14{alpha}(H)-, 5{alpha}(H),14{beta}(H)-, and 5{beta}(H),14{beta}(H)-steranes, double ether- and ester-bonded n-alkanes, and various polynuclear aromatic hydrocarbons, including methylated biphenyls, naphthalenes, phenanthrenes, anthracenes, pyrenes, and chrysenes. However, corresponding coefficients and properties for many more saturated and unsaturated high molecular weight hydrocarbons can be estimated from the equations of state group additivity algorithms

  12. Calculation of the thermodynamic properties at elevated temperatures and pressures of saturated and aromatic high molecular weight solid and liquid hydrocarbons in kerogen, bitumen, petroleum, and other organic matter of biogeochemical interest

    Science.gov (United States)

    Richard, Laurent; Helgeson, Harold C.

    1998-12-01

    To supplement the relatively sparse set of calorimetric data available for the multitude of high molecular weight organic compounds of biogeochemical interest, group additivity algorithms have been developed to estimate heat capacity power function coefficients and the standard molal thermodynamic properties at 25°C and 1 bar of high molecular weight compounds in hydrocarbon source rocks and reservoirs, including crystalline and liquid isoprenoids, steroids, tricyclic diterpenoids, hopanoids, and polynuclear aromatic hydrocarbons. A total of ninety-six group contributions for each coefficient and property were generated from the thermodynamic properties of lower molecular weight reference species for which calorimetric data are available in the literature. These group contributions were then used to compute corresponding coefficients and properties for ˜360 representative solid and liquid high molecular weight compounds in kerogen, bitumen, and petroleum for which few or no experimental data are available. The coefficients and properties of these high molecular weight compounds are summarized in tables, together with those of the groups and reference species from which they were generated. The tabulated heat capacity power function coefficients and standard molal thermodynamic properties at 25°C and 1 bar include selected crystalline and liquid regular, irregular and highly branched isoprenoids, tricyclic diterpanes, 17α(H)- and 17β(H)-hopanes, 5α(H),14α(H)-, 5β(H),14α(H)-, 5α(H),14β(H)-, and 5β(H),14β(H)-steranes, double ether- and ester-bonded n-alkanes, and various polynuclear aromatic hydrocarbons, including methylated biphenyls, naphthalenes, phenanthrenes, anthracenes, pyrenes, and chrysenes. However, corresponding coefficients and properties for many more saturated and unsaturated high molecular weight hydrocarbons can be estimated from the equations of state group additivity algorithms. Calculations of this kind permit comprehensive

  13. A Potential Impact on the Chemical Composition in the Marine Boundary Layer in the Arctic Ocean by Ship Emissions

    Science.gov (United States)

    Xie, Z.; Wang, X.; Blum, J. D.; Sun, L.

    2005-12-01

    Samples of aerosols in the marine boundary layer (MBL) of the Arctic Ocean were collected aboard R/V ()Xuelong during the summer on the Second Chinese Arctic Research Expedition (July-September, 2003). Chemical compositions including major and trace elements and polycyclic aromatic hydrocarbons (PAHs) in aerosol particles were analyzed. Results showed that significant amounts of S, Fe, V and Ni are emitted from ship diesel engines and contaminate the ambient air. The total amount of Fe, which plays a significant role in the ocean ()biological pump, emitted from ships in the Arctic is estimated at 4.33-A106 kg yr-1. Sulfur emitted into the atmosphere may be transformed to sulfur acid and result in a chlorine depletion in sea-salt. Because the global inventory of sulfur from ship exhausts is large and halogens may have important consequences in possible tropospheric ozone destruction, the role of ships in effecting halogen depression in sea-salt should be evaluated. For organic compounds, 17 PAHs including Fluoranthene, Phenanthrene, Chrysene, Indeno[123-cd]pyrene, Pyrene, Benzo[b]fluoranthene, Benzo[ghi]pyrene, Naphthalene, Benzo[a]anthracene, Benzo[k]fluoranthene, Coronene, Fluorene, Benzo[a]pyrene, Acenaphthene, Anthracene, Dibenzo[a,h]anthracene and Acenaphthylene were detected. The average levels of subspecies of PAHs in ambient air ranged from 0.003 to 0.089 ng/m3. Among the 17 PAHs, fluoranthene had a relative high level, while the level of acenaphthylene was relative low. The aerosols contaminated by the ship, which were commonly excluded in previous investigations, thus provide an opportunity to investigate and understand the role of ship emissions in the atmospheric chemistry of the marine boundary layer, especially in the Arctic Ocean.

  14. Acute changes in pulse pressure in relation to constituents of particulate air pollution in elderly persons

    International Nuclear Information System (INIS)

    An increased pulse pressure (difference between systolic and diastolic blood pressure) suggests aortic stiffening. The objective of this study was to examine the acute effects of both particulate matter (PM) mass and composition on blood pressure, among elderly persons. We carried out a panel study in persons living in elderly homes in Antwerp, Belgium. We recruited 88 non-smoking persons, 70% women with a mean age of 83 years (standard deviation: 5.2). Blood pressure was measured and a blood sample was collected on two time points, which were chosen so that there was an exposure contrast in ambient PM exposure. The elemental content of the collected indoor and outdoor PM2.5 (particulate matter with an aerodynamic diameter 10 (particulate matter with an aerodynamic diameter 2.5 was associated with an increase in pulse pressure of 4.0 mmHg (95% confidence interval: 1.8–6.2), in persons taking antihypertensive medication (n=57), but not in persons not using antihypertensive medication (n=31) (p for interaction: 0.02). Vanadium, iron and nickel contents of PM2.5 were significantly associated with systolic blood pressure and pulse pressure, among persons on antihypertensive medication. Similar results were found for indoor concentrations. Of the oxy-PAHs, chrysene-5,6-dione and benzo[a]pyrene-3,6-dione were significantly associated with increases in systolic blood pressure and pulse pressure. In elderly, pulse pressure was positively associated with acute increases in outdoor and indoor air pollution, among persons taking antihypertensive medication. These results might form a mechanistic pathway linking air pollution as a trigger of cardiovascular events.

  15. Interactions between zooplankton and crude oil: toxic effects and bioaccumulation of polycyclic aromatic hydrocarbons.

    Directory of Open Access Journals (Sweden)

    Rodrigo Almeda

    Full Text Available We conducted ship-, shore- and laboratory-based crude oil exposure experiments to investigate (1 the effects of crude oil (Louisiana light sweet oil on survival and bioaccumulation of polycyclic aromatic hydrocarbons (PAHs in mesozooplankton communities, (2 the lethal effects of dispersant (Corexit 9500A and dispersant-treated oil on mesozooplankton, (3 the influence of UVB radiation/sunlight exposure on the toxicity of dispersed crude oil to mesozooplankton, and (4 the role of marine protozoans on the sublethal effects of crude oil and in the bioaccumulation of PAHs in the copepod Acartia tonsa. Mortality of mesozooplankton increased with increasing oil concentration following a sigmoid model with a median lethal concentration of 32.4 µl L(-1 in 16 h. At the ratio of dispersant to oil commonly used in the treatment of oil spills (i.e. 1∶20, dispersant (0.25 µl L(-1 and dispersant-treated oil were 2.3 and 3.4 times more toxic, respectively, than crude oil alone (5 µl L(-1 to mesozooplankton. UVB radiation increased the lethal effects of dispersed crude oil in mesozooplankton communities by 35%. We observed selective bioaccumulation of five PAHs, fluoranthene, phenanthrene, pyrene, chrysene and benzo[b]fluoranthene in both mesozooplankton communities and in the copepod A. tonsa. The presence of the protozoan Oxyrrhis marina reduced sublethal effects of oil on A. tonsa and was related to lower accumulations of PAHs in tissues and fecal pellets, suggesting that protozoa may be important in mitigating the harmful effects of crude oil exposure in copepods and the transfer of PAHs to higher trophic levels. Overall, our results indicate that the negative impact of oil spills on mesozooplankton may be increased by the use of chemical dispersant and UV radiation, but attenuated by crude oil-microbial food webs interactions, and that both mesozooplankton and protozoans may play an important role in fate of PAHs in marine environments.

  16. Naphthalimides Induce G2 Arrest Through the ATM-Activated Chk2-Executed Pathway in HCT116 Cells

    Directory of Open Access Journals (Sweden)

    Hong Zhu

    2009-11-01

    Full Text Available Naphthalimides, particularly amonafide and 2-(2-dimethylamino-6-thia-2-aza-benzo[def]chrysene-1,3-diones (R16, have been identified to possess anticancer activities and to induce G2-M arrest through inhibiting topoisomerase II accompanied by Chk1 degradation. The current study was designed to precisely dissect the signaling pathway(s responsible for the naphthalimide-induced cell cycle arrest in human colon carcinoma HCT116 cells. Using phosphorylated histone H3 and mitotic protein monoclonal 2 as mitosis markers, we first specified the G2 arrest elicited by the R16 and amonafide. Then, R16 and amonafide were revealed to induce phosphorylation of the DNA damage sensor ataxia telangiectasia-mutated (ATM responding to DNA double-strand breaks (DSBs. Inhibition of ATM by both the pharmacological inhibitor caffeine and the specific small interference RNA (siRNA rescued the G2 arrest elicited by R16, indicating its ATM-dependent characteristic. Furthermore, depletion of Chk2, but not Chk1 with their corresponding siRNA, statistically significantly reversed the R16- and amonafide-triggered G2 arrest. Moreover, the naphthalimides phosphorylated Chk2 in an ATM-dependent manner but induced Chk1 degradation. These data indicate that R16 and amonafide preferentially used Chk2 as evidenced by the differential ATM-executed phosphorylation of Chk1 and Chk2. Thus, a clear signaling pathway can be established, in which ATM relays the DNA DSBs signaling triggered by the naphthalimides to the checkpoint kinases, predominantly to Chk2,which finally elicits G2 arrest. The mechanistic elucidation not only favors the development of the naphthalimides as anticancer agents but also provides an alternative strategy of Chk2 inhibition to potentiate the anticancer activities of these agents.

  17. Diurnal variation of particle-bound PAHs in an urban area of Spain using TD-GC/MS: Influence of meteorological parameters and emission sources

    Science.gov (United States)

    Elorduy, I.; Elcoroaristizabal, S.; Durana, N.; García, J. A.; Alonso, L.

    2016-08-01

    Short -term particulate concentrations of 13 polycyclic aromatic hydrocarbons (PAHs) in PM10 were determined in the urban area of Bilbao (Spain). The analysis was performed by thermal desorption coupled with gas chromatography-mass spectrometry (TD-GC/MS), which enabled to use three diurnal periods of 8 h sampling basis time resolution. A total of 105 PM10 samples were collected during 5 months in 2013. Diurnal average concentration of total PAHs (∑13 PAHs) ranged from 1.18 to 9.78 ng m-3; and from 0.06 to 0.70 ng m-3 for benzo[a]pyrene. The presence of high concentrations of benzo[b]fluoranthene, pyrene, fluoranthene and chrysene, and the significant PAHs diurnal variations due to the sampling period, pointed out the influence of mixing anthropogenic sources and meteorological conditions. The diurnal pattern of source contributions was assessed by binary diagnostic ratios and principal component analysis (PCA). These results showed the prevalence of pyrogenic sources coming from traffic and coal/coke combustion sources. Moreover, the PCA differentiated a diurnal pattern of source contributions. The influence of meteorological factors was studied by Pearson correlation analysis and multiple linear regression. Three factors, temperature, wind speed and atmospheric pressure, were identified as the most significant ones affecting diurnal PAHs concentrations. Finally, PCA of the PAHs levels, regulated atmospheric pollutants and meteorological parameters showed that diurnal PAHs concentrations were mainly influenced by variations in the emission sources, atmospheric oxidants such as ozone, and temperature conditions. These results provide further insight into the PAHs diurnal patterns in urban areas by using higher temporal resolutions.

  18. Chemical characterization and stable carbon isotopic composition of particulate polycyclic aromatic hydrocarbons issued from combustion of 10 Mediterranean woods

    Directory of Open Access Journals (Sweden)

    A. Guillon

    2012-08-01

    Full Text Available The objectives of this study were to characterize polycyclic aromatic hydrocarbons from particulate matter emitted during wood combustion and to determine, for the first time, the isotopic signature of PAHs from nine wood species and Moroccan coal from the Mediterranean Basin. In order to differentiate sources of particulate-PAHs, molecular and isotopic measurements of PAHs were performed on the set of wood samples for a large panel of compounds. Molecular profiles and diagnostic ratios were measured by gas chromatography coupled with a mass spectrometer (GC/MS and molecular isotopic compositions (δ13C of particulate-PAHs were determined by gas chromatography/combustion/isotope ratio mass spectrometry (GC/C/IRMS. Wood species present similar molecular profiles with benz(aanthracene and chrysene as dominant PAHs, whereas levels of concentrations range from 1.8 to 11.4 mg g−1 OC (sum of PAHs. Diagnostic ratios are consistent with reference ratios from literature but are not sufficient to differentiate the different species of woods. Concerning isotopic methodology, PAH molecular isotopic compositions are specific for each species and contrary to molecular fingerprints, significant variations of δ13C are observed for the panel of PAHs. This work allows differentiating wood combustion from others origins of particulate matter (vehicular exhaust using isotopic measurements (with δ13CPAH = −28.7 to −26.6‰ but also confirms the necessity to investigate source characterisation at the emission in order to help and complete source assessment models. These first results on woodburnings will be useful for the isotopic approach of source tracking.

  19. Exposure to polycyclic aromatic hydrocarbons (PAHs) and bladder cancer: evaluation from a gene-environment perspective in a hospital-based case-control study in the Canary Islands (Spain)

    Science.gov (United States)

    Boada, Luis D; Henríquez-Hernández, Luis A; Navarro, Patricio; Zumbado, Manuel; Almeida-González, Maira; Camacho, María; Álvarez-León, Eva E; Valencia-Santana, Jorge A; Luzardo, Octavio P

    2015-01-01

    Background: Exposure to polycyclic aromatic hydrocarbons (PAHs) has been linked to bladder cancer. Objective: To evaluate the role of PAHs in bladder cancer, PAHs serum levels were measured in patients and controls from a case-control study. Methods: A total of 140 bladder cancer patients and 206 healthy controls were included in the study. Sixteen PAHs were analyzed from the serum of subjects by gas chromatography–mass spectrometry. Results: Serum PAHs did not appear to be related to bladder cancer risk, although the profile of contamination by PAHs was different between patients and controls: pyrene (Pyr) was solely detected in controls and chrysene (Chry) was exclusively detected in the cases. Phenanthrene (Phe) serum levels were inversely associated with bladder cancer (OR = 0·79, 95%CI = 0·64–0·99, P = 0·030), although this effect disappeared when the allelic distribution of glutathione-S-transferase polymorphisms of the population was introduced into the model (multinomial logistic regression test, P = 0·933). Smoking (OR = 3·62, 95%CI = 1·93–6·79, P<0·0001) and coffee consumption (OR = 1·73, 95%CI = 1·04–2·86, P = 0·033) were relevant risk factors for bladder cancer. Conclusions: Specific PAH mixtures may play a relevant role in bladder cancer, although such effect seems to be highly modulated by polymorphisms in genes encoding xenobiotic-metabolizing enzymes. PMID:25291984

  20. CHARACTERIZATION OF HEXANE SOLUBLE OILS FROM LIQUEFACTION OF TWO BITUMINOUS COALS%两种烟煤的液化及液化油的组成特征研究

    Institute of Scientific and Technical Information of China (English)

    朱继升; LawrenceP.Norcio

    2001-01-01

    Two high-volatile subbituminous coals, DECS-6 of US and Yanzhou coal of China, were liquefied or co-liquefied with HDPE or PVC at 400?℃, 30?min under 7?MPa hydrogen. The results show that Yanzhou coal is easier to be liquefied or co-liquefied than DECS-6 coal under the experimental conditions used and the hexane-soluble oil from Yanzhou coal has more low boiling point fractions than that from DECS-6 coal. The aromatics in hexane soluble oils mainly consist of alkylbeneze, alkylnaphthalene, phenanthrene-,pyrene-, chrysene-, and benzopyrene- compounds, the polars mainly compose of compounds containing O, S and N etc.%在400 ℃、30 min、7 MPa冷氢压条件下两种煤液化结果表明,兖州煤比DECS-6(美国煤)煤更容易液化或共液化,这可能与兖州煤硫含量比较高有关,但DECS-6煤的油收率要高于兖州煤,表明EDCS-6煤容易裂解生成小分子化合物。同种煤液化油的沸点分布特征基本一致。UV(紫外光谱)特征表明,液化油中单环芳烃主要为烷基取代苯类化合物,二环芳烃组分主要是烷基取代萘类化合物,三环芳烃主要为渺位缩合的菲类化合物,四环芳烃主要为芘、屈艹类化合物,五环芳烃以苯并芘类化合物为主,而极性化合物可归属为含O、S、N的极性芳香化合物。

  1. Validación de un método de análisis para la determinación de hidrocarburos aromáticos policíclicos por cromatografía líquida de alta eficiencia en partículas PM10 Y PM2,5 Validation of an analytical method for the determination of polycyclic aromatic hydrocarbons by high efficiency liquid chromatography in PM10 and PM2, 5

    Directory of Open Access Journals (Sweden)

    Jorge Herrera Murillo

    2012-11-01

    Full Text Available Se validó un método analítico para la determinación de hidrocarburos aromáticos policíclicos presentes en partículas PM10 y PM 2,5 recolectadas en el aire mediante cromatografía líquida de alta resolución (CLAR. Los HPA incluidos en la metodología comprenden: Naftaleno, Acenaftileno, Fluoreno, Acenafteno, Fenantreno, Antraceno, Fluoranteno, Pireno, Benzo (aantraceno, Criseno, Benzo (bfluoranteno, Benzo (kfluoranteno, Benzo (apireno, Dibenzo (a,h antraceno, Benzo (g,h,iperileno y Indeno (1,2,3- C.D pireno. Para estos compuestos, los límites de detección y cuantificación estuvieron entre 0,02 y 0,1 mg/l utilizando un equipo marca Dionex modelo ICS- 3000, el cual consta de dos detectores en serie, un ultravioleta modelo VWD-1 y un detector de fluorescencia modelo RF-2000, permitiendo diferenciar las distintas señales de absorción y emisión para la debida identificación de los distintos compuestos. Para todos los compuestos analizados, el factor de recuperación resultó no ser significativamente diferente de uno y la repetibilidad y reproducibilidad resultó ser adecuada para un método analítico, especialmente para los HPA más ligeros.An analytical method for polycyclic aromatic hydrocarbons in PM10 and PM 2.5 par ticles collected from air by high performance liquid chromatography (HPLC was validated. The PAHs analyzed in the methodology include: Naphthalene, Acenaphthylene, Fluorene, Acenaphthene, Phenanthrene, Anthracene, fluoranthene,pyrene,Benzo(aanthracene,Chrysene, Benzo (bfluoranthene, Benzo (kfluoranthene, Benzo (apyrene Dibenzo (a, hanthracene, Benzo (g, h, iperylene and Indeno (1,2,3-CDpyrene. For these compounds, the detection limit and quantification limit were between 0,02 and 0,1 mg/l using a DIONEX ICS 3000 model cromatograph, that has two in serie detectors: UV/Vis and Fluorescense, separating the different absorption and emission signals for proper identification of individual compounds. For all the compounds

  2. The differences in transformation mechanism in natural and anthropogenic PAH in environmental system

    International Nuclear Information System (INIS)

    mg/L): Naphthalene-269,65; Acenaphthene+Fluorene -10,71; Phenanthrene-167,27; Anthracene-2,47; Fluoranthene-170,76; Benzo (a) anthracene-10,61; Chrysene-66,59; Benzo (b) fluoranthene-25,65; Benzo (k) fluoranthene-3,22; Benzo (a) pyrene-0,49; Dibenzo (a, h) anthracene-18,68; Indeno (1,2,3-cd) pyrene-6,13. For comparison were investigated near 50 samples of oil polluted soils selected from oilfield sites and was determined background level of PAH around of oilfields in radius of 700-1000 m

  3. Accumulation and Clearance of PAHs and CYP1A Levels in Farmed Green Mussels (Perna viridis L. from a Coastal Industrial Area in Thailand

    Directory of Open Access Journals (Sweden)

    Varaporn Cholumpai

    2015-07-01

    Full Text Available Green mussels (Perna viridis L. that inhabit along coastal areas with established petro-chemical industries are likely to be exposed to petroleum hydrocarbons. In year 2011, polycyclic aromatic hydrocarbons (PAHs accumulated (i.e. total of 16 PAH congeners in three different sizes of farmed mussels in the Maptaphut industrial estate which is an industrial park in the Gulf of Thailand. The levels of mean total PAHs (0.4303 ± 0.3067 µg/g dry weight in large sized (consumable size mussels were 16 and 8 times higher than medium and small sized mussels. Levels of total carcinogenic PAHs (0.0311± 0.0310 µg/g dry weight in consumable size mussels were 15 and 11 times higher compared to medium and small sized mussels. Two carcinogenic PAHs (i.e. chrysene and benzo[a]anthracene were detected in all sized mussels. The ratio of high molecular weight versus low molecular weight PAHs in all sized mussels indicated the presence of pyrogenic PAHs contamination over petrogenic PAHs in this coastal area. Further studies were carried out in year 2012 involved depuration in consumable sized mussels and effects on the cytochrome P450 1A (CYP1A biomarker were analyzed over a 30 day depuration period. The half-life was five days for total PAH burden (0.4765 ± 0.0615 µg/g dry weight, which included four non-carcinogenic PAHs. After 10, 15 and 30 days depuration in clean water, the mean total PAHs levels decreased gradually but yet significantly (0.2501 ± 0.0186, 0.1350 ± 0.0122 and 0.1554 ± 0.0353 µg/g dry weight, respectively compared to the PAH levels at day 0. Levels of CYP1A declined accordingly and at 30 days depuration CYP1A protein levels were significantly reduced by almost 3-fold compared the PAH levels in mussels from the Maptaphut industrial estate. The results show that farmed green mussels reared for human consumptions are exposed to PAHs including carcinogenic PAHs and that clearance of these PAHs is evident at 30 days depuration. This study

  4. Heat and PAHs Emissions in Indoor Kitchen Air and Its Impact on Kidney Dysfunctions among Kitchen Workers in Lucknow, North India.

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    Amarnath Singh

    Full Text Available Indoor air quality and heat exposure have become an important occupational health and safety concern in several workplaces including kitchens of hotels. This study investigated the heat, particulate matter (PM, total volatile organic compounds (TVOCs and polycyclic aromatic hydrocarbons (PAHs emissions in indoor air of commercial kitchen and its association with kidney dysfunctions among kitchen workers. A cross sectional study was conducted on 94 kitchen workers employed at commercial kitchen in Lucknow city, North India. A questionnaire-based survey was conducted to collect the personal and occupational history of the kitchen workers. The urine analysis for specific gravity and microalbuminuria was conducted among the study subjects. Indoor air temperature, humidity, wet/ dry bulb temperature and humidex heat stress was monitored during cooking activities at the kitchen. Particulate matter (PM for 1 and 2.5 microns were monitored in kitchen during working hours using Hazdust. PAHS in indoor air was analysed using UHPLC. Urinary hydroxy-PAHs in kitchen workers were measured using GC/MS-MS. Higher indoor air temperature, relative humidity, PM1 and PM2.5 (p<0.001 was observed in the kitchen due to cooking process. Indoor air PAHs identified are Napthalene, fluorine, acenaphthene, phenanthrene, pyrene, chrysene and indeno [1,2,3-cd pyrene. Concentrations of all PAHs identified in kitchen were above the permissible OSHA norms for indoor air. Specific gravity of urine was significantly higher among the kitchen workers (p<0.001 as compared to the control group. Also, the prevalence of microalbuminuria was higher (p<0.001 among kitchen workers. Urinary PAH metabolites detected among kitchen workers were 1-NAP, 9-HF, 3-HF, 9-PHN and 1-OHP. Continuous heat exposure in kitchens due to cooking can alter kidney functions viz., high specific gravity of urine in kitchen workers. Exposure to PM, VOCs and PAHs in indoor air and presence of urinary PAHs

  5. Application of a fuzzy neural network model in predicting polycyclic aromatic hydrocarbon-mediated perturbations of the Cyp1b1 transcriptional regulatory network in mouse skin

    Energy Technology Data Exchange (ETDEWEB)

    Larkin, Andrew [Department of Environmental and Molecular Toxicology, Oregon State University (United States); Department of Statistics, Oregon State University (United States); Superfund Research Center, Oregon State University (United States); Siddens, Lisbeth K. [Department of Environmental and Molecular Toxicology, Oregon State University (United States); Superfund Research Center, Oregon State University (United States); Krueger, Sharon K. [Superfund Research Center, Oregon State University (United States); Linus Pauling Institute, Oregon State University (United States); Tilton, Susan C.; Waters, Katrina M. [Superfund Research Center, Oregon State University (United States); Computational Biology and Bioinformatics Group, Pacific Northwest National Laboratory, Richland, WA 99352 (United States); Williams, David E., E-mail: david.williams@oregonstate.edu [Department of Environmental and Molecular Toxicology, Oregon State University (United States); Superfund Research Center, Oregon State University (United States); Linus Pauling Institute, Oregon State University (United States); Environmental Health Sciences Center, Oregon State University, Corvallis, OR 97331 (United States); Baird, William M. [Department of Environmental and Molecular Toxicology, Oregon State University (United States); Superfund Research Center, Oregon State University (United States); Environmental Health Sciences Center, Oregon State University, Corvallis, OR 97331 (United States)

    2013-03-01

    Polycyclic aromatic hydrocarbons (PAHs) are present in the environment as complex mixtures with components that have diverse carcinogenic potencies and mostly unknown interactive effects. Non-additive PAH interactions have been observed in regulation of cytochrome P450 (CYP) gene expression in the CYP1 family. To better understand and predict biological effects of complex mixtures, such as environmental PAHs, an 11 gene input-1 gene output fuzzy neural network (FNN) was developed for predicting PAH-mediated perturbations of dermal Cyp1b1 transcription in mice. Input values were generalized using fuzzy logic into low, medium, and high fuzzy subsets, and sorted using k-means clustering to create Mamdani logic functions for predicting Cyp1b1 mRNA expression. Model testing was performed with data from microarray analysis of skin samples from FVB/N mice treated with toluene (vehicle control), dibenzo[def,p]chrysene (DBC), benzo[a]pyrene (BaP), or 1 of 3 combinations of diesel particulate extract (DPE), coal tar extract (CTE) and cigarette smoke condensate (CSC) using leave-one-out cross-validation. Predictions were within 1 log{sub 2} fold change unit of microarray data, with the exception of the DBC treatment group, where the unexpected down-regulation of Cyp1b1 expression was predicted but did not reach statistical significance on the microarrays. Adding CTE to DPE was predicted to increase Cyp1b1 expression, whereas adding CSC to CTE and DPE was predicted to have no effect, in agreement with microarray results. The aryl hydrocarbon receptor repressor (Ahrr) was determined to be the most significant input variable for model predictions using back-propagation and normalization of FNN weights. - Highlights: ► Tested a model to predict PAH mixture-mediated changes in Cyp1b1 expression ► Quantitative predictions in agreement with microarrays for Cyp1b1 induction ► Unexpected difference in expression between DBC and other treatments predicted ► Model predictions

  6. Exposure of children to air pollution in the industrial zone of Metropolitan Area of Mexico City

    Science.gov (United States)

    Mugica-Alvarez, Violeta; Quintanilla-Vega, Betsabé; De Vizcaya-Ruiz, Andrea; Alvarado-Cruz, Isabel

    2016-04-01

    An air quality monitoring in three schools located in the most important industrial zone at the Northeast of the Metropolitan Area of Mexico City (MAMC) was conducted in order to determine the exposure of children to toxics contained in PM10. Particles were analyzed for metals, polycyclic aromatic hydrocarbons (PAH), organic and elemental carbon by ICP-AES, GC-MS and TOT (Sunset lab) respectively. Average concentration of PM10 was 108.4±11.6 μg/m3. Most abundant metals were Fe, Zn and Pb with concentrations ranged by 1.1-5.4 μg/m3, 0.3-2 μg/m3, and 0.18-0.63 μg/m3 respectively; the sum of the seventeen PAHs varied from 1.4 to 3.3 ng/m3 where most abundant PAH were indene[1,2,3-c,d]pyrene, benzo[b]fluoranthene, benzo[a]anthracene, chrysene, and benzo[a]pyrene. The sum of the seven carcinogenic PAH contributed in average with the 48% of the total mixture. Carcinogenic potential of PAH were obtained using toxic equivalent factors determined by Nisbet and La Goy which varied from 0.3 to 0.6 ng/ m3 of benzo[a]pyrene equivalent (BAPeq), this value is lower than the standard proposed for the European Community of 1 ng/ m3, but higher than the standard from the United Kingdom of 0.25 ng/ m3. Principal component analysis for source apportionment showed that vehicular and industrial emissions are the main sources of PM in the zone. In general, the concentrations of particles as well as concentration of metals and PAHs are lower than concentrations measured six year before, showing that the established measures have improved the air quality. Nevertheless these PM10 concentrations exceeded frequently the Mexican Standard and children are especially susceptible due to the higher risk to develop diseases if the exposure occurs at early age.

  7. Long term observations of PM2.5-associated PAHs: Comparisons between normal and episode days

    Science.gov (United States)

    Wang, Jia; Li, Xiao; Jiang, Nan; Zhang, Wenkai; Zhang, Ruiqin; Tang, Xiaoyan

    2015-03-01

    The pollution characteristic of fine particular matter (PM2.5) and associated polycyclic aromatic hydrocarbons (PAHs) are currently drawing a great deal of interest because of their influence on environment and health. In this study, PM2.5 was collected from 2011 to 2013 (n = 188) in a suburban area of Zhengzhou, China. 16-PAHs were analyzed to determine the concentration, seasonal variation and potential sources during normal days and episode events. The total mass of 16 PAHs and PM2.5 were in the range of 7-961 ng m-3 and 55-697 μg m-3, with a 3-year average of 174 ng m-3 and 194 μg m-3 respectively. Winter is most polluted for both PM2.5 and PAHs. Average PAH and PM2.5 concentrations during three episode events are 454 ng m-3 and 453 μg m-3, respectively, much higher than values during normal days (299 ng m-3 and 180 μg m-3, respectively). Ratios of Σ16PAH/PM2.5 varied with seasons and concentrations of PM2.5, but showed a negative correlation with PM2.5 concentrations during episode events. The dominant components of PAHs are Benzo[b]fluoranthene, Chrysene, Fluoranthene, and Benzo[k]fluoranthene, Benz[a]anthracene, Pyrene, Indeno(1,2,3-cd)pyrene and their total concentrations vary from 27 to 342 ng m-3, accounting for 58-82% (average = 73%) of 16 PAHs. The Benzo[a]pyrene (Bap) concentration obtained was 9.4 ng m-3 (3-year average), exceeding nearly one order of magnitude of ambient air BaP standard (annual average: 1.0 ng m-3) in China. Diagnose ratios and Positive Matrix Factorization results show that coal combustion, vehicles, coking plant, and biomass burning are main sources for PAHs in this area. The high concentrations of PM2.5 and PAHs, especially during episode events, reflected a potential health problem for nearby public and the necessity of air pollution control for both stationary and mobile sources.

  8. Hidrocarbonetos policíclicos aromáticos (HPAs em aguardentes PHAs in spirits

    Directory of Open Access Journals (Sweden)

    S. M. Bettin

    2005-06-01

    Full Text Available A presença de hidrocarbonetos aromáticos polinucleares (HPAs em aguardentes foi investigada por cromatografia líquida (CLAE após sua prévia extração em fase sólida (SPE. A separação foi realizada em uma coluna Supelco, LCPAH-octadecil silano (25cm x 4,6mm x 5mm com gradiente acetonitrila/água e a quantificação utilizando detector de fluorescência. Os HPAs (naftaleno; acenaftaleno; fluoreno; fenantreno; antraceno; fluoranteno; pireno; 1,2- benzo(epireno; criseno; benzo(epireno; 2,3-benzo(aantraceno; 1,2-benzo(bfluoranteno; benzo(kfluoranteno; dibenzo(a,hantraceno; benzo(apireno; benzo(ghipirileno foram identificados e quantificados em vinte e oito amostras de aguardentes de cana. Os resultados experimentais para as amostras de aguardentes (cachaças são analisados em termos de análises de componentes principais (PCA objetivando a diferenciação entre o perfil das aguardentes produzidas a partir de cana-de-açúcar queimada e não-queimada.The presence of PHAs (polycyclic aromatic hydrocabons in spirits has been investigated using high performance liquid chromatography (HPLC after solid phase extraction (SPE. The separation was achieved with a Supelco LCPAH-octadecil silane column [25cm x 4,6mm x 5mm] and acetonitrile/water elution gradient and the quantification using a fluorescence detector. The PHAs (naphthalene; acenaphthene; fluorene; phenantrene; anthracene; phuorantene; pyrene; 1,2-benzo(epyrene; chrysene; benzo(epyrene; 2,3-benzo(aanthracene; 1,2-benzo(bphluoranthene; benzo(kfluoranthene; dibenzo(a,hanthracene; benzo(apyreno; benzo(ghipyrilene were quantifed in twenty eight samples of sugar cane spirits. All the experimental data for sugar cane spirit have been analyzed through principal components analysis (PCA aiming to compare the chemical profile of beverages produced from burned and not burned sugar cane.

  9. Influence of tobacco smoke on carcinogenic PAH composition in indoor PM 10 and PM 2.5

    Science.gov (United States)

    Slezakova, K.; Castro, D.; Pereira, M. C.; Morais, S.; Delerue-Matos, C.; Alvim-Ferraz, M. C.

    2009-12-01

    Because of the mutagenic and/or carcinogenic properties, Polycyclic Aromatic Hydrocarbons (PAH), have a direct impact on human population. Consequently, there is a widespread interest in analysing and evaluating the exposure to PAH in different indoor environments, influenced by different emission sources. The information on indoor PAH is still limited, mainly in terms of PAH distribution in indoor particles of different sizes; thus, this study evaluated the influence of tobacco smoke on PM 10 and PM 2.5 characteristics, namely on their PAH compositions, with further aim to understand the negative impact of tobacco smoke on human health. Samples were collected at one site influenced by tobacco smoke and at one reference (non-smoking) site using low-volume samplers; the analyses of 17 PAH were performed by Microwave Assisted Extraction combined with Liquid Chromatography (MAE-LC). At the site influenced by tobacco smoke PM concentrations were higher 650% for PM 10, and 720% for PM 2.5. When influenced by smoking, 4 ring PAH (fluoranthene, pyrene, and chrysene) were the most abundant PAH, with concentrations 4600-21 000% and 5100-20 800% higher than at the reference site for PM 10 and PM 2.5, respectively, accounting for 49% of total PAH (Σ PAH). Higher molecular weight PAH (5-6 rings) reached concentrations 300-1300% and 140-1700% higher for PM 10 and PM 2.5, respectively, at the site influenced by tobacco smoke. Considering 9 carcinogenic PAH this increase was 780% and 760% in PM 10 and PM 2.5, respectively, indicating the strong potential risk for human health. As different composition profiles of PAH in indoor PM were obtained for reference and smoking sites, those 9 carcinogens represented at the reference site 84% and 86% of Σ PAH in PM 10 and PM 2.5, respectively, and at the smoking site 56% and 55% of Σ PAH in PM 10 and PM 2.5, respectively. All PAH (including the carcinogenic ones) were mainly present in fine particles, which corresponds to a strong risk

  10. 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

  11. Structural investigations of the ferredoxin and terminal oxygenase components of the biphenyl 2,3-dioxygenase from Sphingobium yanoikuyae B1

    Directory of Open Access Journals (Sweden)

    Gibson David T

    2007-03-01

    Full Text Available Abstract Background The initial step involved in oxidative hydroxylation of monoaromatic and polyaromatic compounds by the microorganism Sphingobium yanoikuyae strain B1 (B1, previously known as Sphingomonas yanoikuyae strain B1 and Beijerinckia sp. strain B1, is performed by a set of multiple terminal Rieske non-heme iron oxygenases. These enzymes share a single electron donor system consisting of a reductase and a ferredoxin (BPDO-FB1. One of the terminal Rieske oxygenases, biphenyl 2,3-dioxygenase (BPDO-OB1, is responsible for B1's ability to dihydroxylate large aromatic compounds, such as chrysene and benzo[a]pyrene. Results In this study, crystal structures of BPDO-OB1 in both native and biphenyl bound forms are described. Sequence and structural comparisons to other Rieske oxygenases show this enzyme to be most similar, with 43.5 % sequence identity, to naphthalene dioxygenase from Pseudomonas sp. strain NCIB 9816-4. While structurally similar to naphthalene 1,2-dioxygenase, the active site entrance is significantly larger than the entrance for naphthalene 1,2-dioxygenase. Differences in active site residues also allow the binding of large aromatic substrates. There are no major structural changes observed upon binding of the substrate. BPDO-FB1 has large sequence identity to other bacterial Rieske ferredoxins whose structures are known and demonstrates a high structural homology; however, differences in side chain composition and conformation around the Rieske cluster binding site are noted. Conclusion This is the first structure of a Rieske oxygenase that oxidizes substrates with five aromatic rings to be reported. This ability to catalyze the oxidation of larger substrates is a result of both a larger entrance to the active site as well as the ability of the active site to accommodate larger substrates. While the biphenyl ferredoxin is structurally similar to other Rieske ferredoxins, there are distinct changes in the amino acids near

  12. Heat and PAHs Emissions in Indoor Kitchen Air and Its Impact on Kidney Dysfunctions among Kitchen Workers in Lucknow, North India.

    Science.gov (United States)

    Singh, Amarnath; Kamal, Ritul; Mudiam, Mohana Krishna Reddy; Gupta, Manoj Kumar; Satyanarayana, Gubbala Naga Venkata; Bihari, Vipin; Shukla, Nishi; Khan, Altaf Hussain; Kesavachandran, Chandrasekharan Nair

    2016-01-01

    Indoor air quality and heat exposure have become an important occupational health and safety concern in several workplaces including kitchens of hotels. This study investigated the heat, particulate matter (PM), total volatile organic compounds (TVOCs) and polycyclic aromatic hydrocarbons (PAHs) emissions in indoor air of commercial kitchen and its association with kidney dysfunctions among kitchen workers. A cross sectional study was conducted on 94 kitchen workers employed at commercial kitchen in Lucknow city, North India. A questionnaire-based survey was conducted to collect the personal and occupational history of the kitchen workers. The urine analysis for specific gravity and microalbuminuria was conducted among the study subjects. Indoor air temperature, humidity, wet/ dry bulb temperature and humidex heat stress was monitored during cooking activities at the kitchen. Particulate matter (PM) for 1 and 2.5 microns were monitored in kitchen during working hours using Hazdust. PAHS in indoor air was analysed using UHPLC. Urinary hydroxy-PAHs in kitchen workers were measured using GC/MS-MS. Higher indoor air temperature, relative humidity, PM1 and PM2.5 (p<0.001) was observed in the kitchen due to cooking process. Indoor air PAHs identified are Napthalene, fluorine, acenaphthene, phenanthrene, pyrene, chrysene and indeno [1,2,3-cd) pyrene. Concentrations of all PAHs identified in kitchen were above the permissible OSHA norms for indoor air. Specific gravity of urine was significantly higher among the kitchen workers (p<0.001) as compared to the control group. Also, the prevalence of microalbuminuria was higher (p<0.001) among kitchen workers. Urinary PAH metabolites detected among kitchen workers were 1-NAP, 9-HF, 3-HF, 9-PHN and 1-OHP. Continuous heat exposure in kitchens due to cooking can alter kidney functions viz., high specific gravity of urine in kitchen workers. Exposure to PM, VOCs and PAHs in indoor air and presence of urinary PAHs metabolites may

  13. [Laser Induced Fluorescence Spectroscopic Analysis of Aromatics from One Ring to Four Rings].

    Science.gov (United States)

    Zhang, Peng; Liu, Hai-feng; Yue, Zong-yu; Chen, Bei-ling; Yao, Ming-fa

    2015-06-01

    In order to distinguish small aromatics preferably, a Nd : YAG Laser was used to supply an excitation laser, which was adjusted to 0.085 J x cm(-2) at 266 nm. Benzene, toluene, naphthalene, phenanthrene, anthracene, pyrene and chrysene were used as the representative of different rings aromatics. The fluorescence emission spectra were researched for each aromatic hydrocarbon and mixtures by Laser induced fluorescence (LIF). Results showed that the rings number determined the fluorescence emission spectra, and the structure with same rings number did not affect the emission fluorescence spectrum ranges. This was due to the fact that the absorption efficiency difference at 266 nm resulted in that the fluorescence intensities of each aromatic hydrocarbon with same rings number were different and the fluorescence intensities difference were more apparently with aromatic ring number increasing. When the absorption efficiency was similar at 266 nm and the concentrations of each aromatic hydrocarbon were same, the fluorescence intensities were increased with aromatic ring number increasing. With aromatic ring number increasing, the fluorescence spectrum and emission peak wavelength were all red-shifted from ultraviolet to visible and the fluorescence spectrum range was also wider as the absorption efficiency was similar. The fluorescence emission spectra from one to four rings could be discriminated in the following wavelengths, 275 to 320 nm, 320 to 375 nm, 375 to 425 nm, 425 to 556 nm, respectively. It can be used for distinguish the type of the polycyclic aromatic hydrocarbons (PAHs) as it exists in single type. As PAHs are usually exist in a variety of different rings number at the same time, the results for each aromatic hydrocarbon may not apply to the aromatic hydrocarbon mixtures. For the aromatic hydrocarbon mixtures, results showed that the one- or two-ring PAHs in mixtures could not be detected by fluorescence as three- or four-ring PAHs existed in mixture

  14. Natural attenuation in contaminated soils with hydrocarbons; Atenuacion natural en suelos contaminados con hidrocarburos

    Energy Technology Data Exchange (ETDEWEB)

    Corona Ramirez, L.; Iturbide Arguelles, R. [Facultad de Ingenieria, UNAM, Mexico, D.F. (Mexico)

    2005-06-01

    A contaminated soil experiment was performed using simples from a refinery, containing oil derivative hydrocarbons, specifically those with high concentrations of polyaromathic hydrocarbons (PAH). The testing consisted in 7 pans with 7 kg of soil, the preparation of 6 pans under specific conditions and one as a blank, the conditions were: water content (15 y 30%), addition a non-ionic surfactant. The process consisted in the daily aeration and water control of the samples. The PAH were analyzed: anthracene, benzo(a) pyrene, chrysene, phenanthrene and naphthalene. The results after 8 weeks showed a gradual degradation of PAH, indicating a better removal obtained when the water content was 30% with nutrients addition. [Spanish] Se realizo un experimento con suelo contaminado proveniente de una refineria, el cual contaba con hidrocarburos derivados de petroleo, especificamente con concentraciones elevadas de hidrocarburos poliaromaticos (HAP). El estudio consistio en preparar 7 cajones con 7 kg de suelo, cada uno con las siguientes condiciones: S1suelo contaminado con hidrocarburos y 15% de contenido de agua. S2 suelo contaminado con hidrocarburo y adicion de Nitrogeno y Fosforo (N y P) con 15% de contenido de agua. S3 suelo contaminado con hidrocarburo y adicion de N y P mas un surfactante no ionico, Emulgin W600, con 15% de contenido de agua. S4 igual a S1 pero con 30% de contenido de agua. S5 igual a S2, con 30% de contenido de agua. S6 igual S3 con 30% de contenido de agua. S7 suelo contaminado testigo, sin control de humedad y sin aireacion. La experimentacion consistio en airear el suelo diariamente y controlar el contenido de agua de manera que este fuera constante. Los resultados, indican que la mejor remocion se obtuvo para el contenido de agua de 30%, con adicion de nutrientes y surfactante. Los compuestos con mayor eficiencia de remocion para todas las opciones son naftaleno y antraceno. Por lo tanto, de acuerdo con los resultados, los compuestos

  15. Characterization of used lubricating oil by spectrometric techniques

    Energy Technology Data Exchange (ETDEWEB)

    Souza, Andressa Moreira de, E-mail: andressa@ctaa.embrapa.br [Embrapa Agroindustria de Alimentos, Guaratiba, Rio de Janeiro, RJ (Brazil); Correa, Sergio Machado [Faculdade de Engenharia. Universidade do Estado do Rio de Janeiro (UERJ), Resende, RJ (Brazil); Silva, Glauco Correa da [Instituto de Engenharia Nuclear (IEN/CNEN-RJ), Rio de Janeiro, RJ (Brazil)

    2011-07-01

    Using GC/FID, USEPA METHOD 8021B - Aromatic and halogenated volatiles by gas chromatography using photoionization and/or electrolytic conductivity detectors e USEPA METHOD 8270C - Semivolatile organic compounds by gas chromatography/mass spectrometry (GC/MS), to identify: Total Petroleum Hydrocarbons (TPH); polyaromatic hydrocarbons (PAHs) - naphthalene, acenaphthylene, acenaphthene , fluorene, phenanthrene, anthracene, fluoranthene, pyrene, benze[a]anthracene and chrysene; benzene, toluene, ethylbenzene and xylenes (BTEX). After characterization of the engine lubricating oil after use allows us to evaluate engine wear and determine oil change interval. (author)

  16. Characterization of used lubricating oil by spectrometric techniques

    International Nuclear Information System (INIS)

    /FID, USEPA METHOD 8021B - Aromatic and halogenated volatiles by gas chromatography using photoionization and/or electrolytic conductivity detectors e USEPA METHOD 8270C - Semivolatile organic compounds by gas chromatography/mass spectrometry (GC/MS), to identify: Total Petroleum Hydrocarbons (TPH); polyaromatic hydrocarbons (PAHs) - naphthalene, acenaphthylene, acenaphthene , fluorene, phenanthrene, anthracene, fluoranthene, pyrene, benze[a]anthracene and chrysene; benzene, toluene, ethylbenzene and xylenes (BTEX). After characterization of the engine lubricating oil after use allows us to evaluate engine wear and determine oil change interval. (author)

  17. Concentrations of polynuclear aromatic hydrocarbons and inorganic constituents in ambient surface soils, Chicago, Illinois, 2001-02

    Science.gov (United States)

    Kay, Robert T.; Arnold, Terri L.; Cannon, William F.; Graham, David; Morton, Eric; Bienert, Raymond

    2003-01-01

    Polynuclear aromatic hydrocarbon (PAH) compounds are ubiquitous in ambient surface soils in the city of Chicago, Illinois. PAH concentrations in samples collected in June 2001 and January 2002 were typically in the following order from highest to lowest: fluoranthene, pyrene, benzo(b)fluoranthene, phenanthrene, benzo(a)pyrene, chrysene, benzo(a)anthracene, benzo(k)fluoranthene, indeno(1,2,3-cd)pyrene, benzo(g,h,i)perylene, dibenzo(a,h)anthracene, and anthracene. Naphthalene, acenaphthene, acenaphthylene, and fluorene were consistently at the lowest concentrations in each sample. Concentrations of the PAH compounds showed variable correlation. Concentrations of PAH compounds with higher molecular weights typically show a higher degree of correlation with other PAH compounds of higher molecular weight, whereas PAH compounds with lower molecular weights tended to show a lower degree of correlation with all other PAH compounds. These differences indicate that high and low molecular-weight PAHs behave differentl y once released into the environment. Concentrations of individual PAH compounds in soils typically varied by at least three orders of magnitude across the city and varied by more than an order of magnitude over a distance of about 1,000 feet. Concentrations of a given PAH in ambient surface soils are affected by a variety of site-specific factors, and may be affected by proximity to industrial areas. Concentrations of a given PAH in ambient surface soils did not appear to be affected the organic carbon content of the soil, proximity to non-industrial land use, or proximity to a roadway. The concentration of the different PAH compounds in ambient surface soils appears to be affected by the propensity for the PAH compound to be in the vapor or particulate phase in the atmosphere. Lower molecular-weight PAH compounds, which are primarily in the vapor phase in the atmosphere, were detected in lower concentrations in the surface soils. Higher molecular-weight PAH

  18. 北京地区表层土壤中多环芳烃的分布特征及污染源分析%Distribution and sources of polycyclic aromatic hydrocarbon compounds in topsoil of Beijing, China

    Institute of Scientific and Technical Information of China (English)

    张枝焕; 卢另; 贺光秀; 彭旭阳; 朱雷; 王新伟; 焦煦

    2011-01-01

    根据北京地区不同环境功能区62个样品的分析结果,讨论了研究区表层土壤中多环芳烃的分布特征及污染源类型.结果表明:(1)研究区表层土壤中检测到的多环芳烃主要包括萘、苊、菲、惹烯、三芴、荧蒽、芘、(屈)、苯并蒽、苯并[b]荧蒽、苯并[K]荧蒽、苯并[e]芘、苯并[a]芘、苝、二苯并[a,h]蒽、茚并[1,2,3-cd]芘、苯并[g,h,i]苝及其同系物;(2)不同环境功能区表层土壤中多环芳烃的组成及质量分数均存在一定的差别,16种优先控制的多环芳烃质量分数为175.1~10 344ng·g-1,其中城市中心区表层土壤中多环芳烃的质量分数最高,交通干线附近、工矿企业附近表层土壤中PAHs的质量分数较高,林地、果园和农田表层土壤中PAHs的质量分数较低;(3)表层土壤中PAHs既有来源于石油源,也有来源于化石燃料燃烧产物的,但不同功能区二者贡献存在差别,其中农业用地(林地、果园、农田)中PAHs主要来源于石油源(或部分来源于土壤母岩中的有机质),城区、交通干线附近及工矿企业附近表层土壤中PAHs污染源以化石燃料燃烧产物输入为主.%Sixty-two topsoil samples collected in Beijing were detected and analyzed.The distribution and contamination sources of Polyeyclic Aromatic Hydrocarbon Compounds (PAHs) were discussed.The results showed that (1) many kinds of PAHs in topsoil samples of Beijing were found, mainly including naphthalene, acenaphthene, phenanthrene, retene, fluorene, dibenzofuran,dibenzothiophene, fluoranthene, pyrene, chrysene, benzanthracene, benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[e]pyrene,benzo[a]pyrene, perylene, dibenzo[a,h]anthracene, indeno[1,2,3-cd]pyrene, benzo[g,h,i]perylene and their homologous compounds;(2) the composition and concentration of PAHs in topsoil samples from different environmental function areas were different.The concentration of sixteen prior pollutants PAHs was between 175

  19. Colémbolos (Hexapoda como bioindicadores de la calidad de suelos contaminados con hidrocarburos en el sureste de México Collembola (Hexapoda as quality bioindicators of the hydrocarburans polluted soils in Southestern Mexico

    Directory of Open Access Journals (Sweden)

    Raúl Uribe-Hernández

    2010-04-01

    , equitativity (J' and the similarity index (S. We also performed the following soil analyses: total petroleum hydrocarbon content (HTP, polycyclic aromatic hydrocarbon content (HAP, porosity, pH, CE, MO, N, P, K, CIC, and texture. In contaminated areas, HTP exceeded the safe limits sets by Mexican environmental legislation. In all studied areas we observed Collembola, mites, and dipteran larvae. The variation in abundance and diversity of these insects can be used as biondicators of the level of contamination and quality of the soil. We found very low abundances of Crustacea, Formicidae, Aranae, Diptera, Pseudoscopionida, and Diplopoda. The Collembola families that were most widely distributed were Sminthurididae and Isotomidae. Our correlation analysis showed that their diversity is affected by HAP level (fluoranthene, naphfhalene, pyrene, chrysene and phenanthrene.

  20. Scavenging ratio of polycyclic aromatic compounds in rain and snow at the Athabasca oil sands region

    Directory of Open Access Journals (Sweden)

    L. Zhang

    2014-07-01

    Full Text Available Athabasca oil sands industry in northern Alberta, Canada is a possible source of polycyclic aromatic compounds (PACs. Monitored PACs, including polycyclic aromatic hydrocarbons (PAHs, alkylated PAHs, and dibenzothiophenes, in precipitation and in air at three near-source sites in the Fort MacKay and Fort McMurray area during May 2011 to August 2012 were analyzed to generate a database of scavenging (or washout ratios (Wt for PACs scavenged by both snow and rain. Median precipitation and air concentrations of parent PAHs over the May 2011 to August 2012 period ranged from 0.3–184.9 (chrysene ng L−1 and 0.01–3.9 (naphthalene ng m−3, respectively, which were comparable to literature values. Higher concentrations in precipitation and air were observed for alkylated PAHs and dibenzothiophenes. The median precipitation and air concentrations were 11.3–646.7 (C3-fluoranthene/pyrene ng L−1 and 0.21–16.9 (C3-naphthalene ng m−3, respectively, for alkylated PAHs, and 8.5–530.5 (C4-dibenzothiophene ng L−1 and 0.13–6.6 (C2-dibenzothiophene ng m−3 for dibenzothiophenes and their alkylated derivatives. Median Wt over the measurement period were 6100–1.1 × 106 from snow scavenging and 350–2.3 × 105 from rain scavenging depending on the PAC species. Median Wt for parent PAHs were within the range of those observed at other urban and suburban locations. But Wt for acenaphthylene in snow samples was 2–7 times higher. Some individual snow and rain samples exceeded literature values by a factor of 10. Wt for benzo(apyrene, dibenz(a,hanthracene, and benzo(g,h,iperylene in snow samples had reached 107, which is the maximum for PAH snow scavenging ratios reported in literature. From the analysis of data subsets, Wt for particulate-phase dominant PACs were 14–20 times greater than gas-phase dominant PACs in snow samples and 7–20 times greater than gas-phase dominant PACs in rain samples. Wt from snow scavenging was ∼9 times greater

  1. Amelioration of soil PAH and heavy metals by combined application of fly ash and biochar

    Science.gov (United States)

    Masto, Reginald; George, Joshy; Ansari, Md; Ram, Lal

    2016-04-01

    Generation of electricity through coal combustion produces huge quantities of fly ash. Sustainable disposal and utilization of these fly ash is a major challenge. Fly ash along with other amendments like biochar could be used for amelioration of soil. In this study, fly ash and biochar were used together for amelioration of polycyclic aromatic hydrocarbon (PAH) contaminated soil. Field experiment was conducted to investigate the effects of fly ash and biochar on the amelioration of soil PAH, and the yield of Zea mays. The treatments were control, biochar (4 t/ha), fly ash (4 t/ha), ash + biochar ( 2 + 2 t/ha). Soil samples were collected after the harvest of maize crop and analysed for chemical and biological parameters. Thirteen PAHs were analysed in the postharvest soil samples. Soil PAHs were extracted in a microwave oven at 120 °C using hexane : acetone (1:1) mixture. The extracted solutions were concentrated, cleaned and the 13 PAHs [Acenaphthene (Ace), fluorene (Flr), phenanthrene (Phn), anthracene(Ant), pyrene(Pyr), benz(a)anthracene (BaA), chrysene (Chy), benzo(b)fluoranthene (BbF), benzo(k)fluoranthene (BkF), benzo(a)pyrene, benzo(g,h,i)perylene (BghiP), dibenzo(a,h)anthracene, and indeno(1,2,3-cd)pyrene)(Inp)] were analysed using GC-MS. The mean pH increased from 6.09 in control to 6.64 and 6.58 at biochar and fly ash treated soils, respectively. N content was not affected, whereas addition of biochar alone and in combination with fly ash, has significantly increased the soil organic carbon content. P content was almost double in combined (9.06 mg/kg) treatment as compared to control (4.32 mg/kg). The increase in K due to biochar was 118%, whereas char + ash increased soil K by 64%. Soil heavy metals were decreased: Zn (‑48.4%), Ni (‑41.4%), Co (‑36.9%), Cu (‑35.7%), Mn (‑34.3%), Cd (‑33.2%), and Pb (‑30.4%). Soil dehydrogenase activity was significantly increased by ash and biochar treatments and the maximum activity was observed for the

  2. 超声波萃取-同步荧光法测定土壤中的多环芳烃研究%Simultaneous determination of polycyclic aromatic hydrocarbons in soft by way of supersonic extraction and synchronous fluorescence spectrometry

    Institute of Scientific and Technical Information of China (English)

    何立芳; 项小燕; 章汝平

    2011-01-01

    -breeding garden soil were mainly dominated by benzo [a] pyrene and fluoranthene, whereas in the Long-zhou Industrial Park in soil were mainly dominated by benzo [a] pyrene, fluoranthene, but benzo [k] fluoranthene, carbazole and chrysene, are used in the soil of Longyan Sande Cement Plant,where the soils were mainly dominated by benzo [a] pyrene, fluoranthene, the Philippines and Anthracene. Since the method is simple and convenient in use, as well as easily be identified and quantitatively determined, it is favorable for the simultaneous, multi-component applications with no need of pre-separation. What is more, real samples will so be made respondent and available upon the direct call.%采用超声波萃取-恒波长同步荧光法测定了土壤中的多环芳烃(PAHs).对超声波萃取和同步荧光法的测定条件进行优化,考察方法的线性相关性、准确性和加标回收率,确定优化条件为:二氯甲烷/正已烷(1∶1),体积每次30 mL分两次提取,提取时间为60 min,样品不需纯化,直接可用于同步荧光分析.超声波萃取效率高,萃取时间短.采用恒波长同步荧光法对多环芳烃进行定性定量,相关系数r>0.9981,检测限0.052~12.37 ng,标准偏差0.017% ~ 4.12%,回收率68.2%~109.9%.采用超声萃取-同步荧光法测定了龙岩市区不同功能区土壤中的多环芳烃.结果表明,闽西监狱良种繁殖园土样中含有苯并[a]芘和荧蒽,龙洲工业园土样中含有苯并[a]芘、荧蒽、苯并[k]荧葸、咔唑和,龙岩三德水泥厂土样中含有苯并[a]芘、荧葸、菲和蒽.该法简便快速,无需对混合物进行分离就可实现多组分的同时鉴别和定量测定.

  3. 百色市工业区表层土壤中多环芳烃污染特征及来源分析%Characteristics and sources of polycyclic aromatic hydrocarbons in surface soil from industrial areas of Baise, Guangxi

    Institute of Scientific and Technical Information of China (English)

    史兵方; 吴启琳; 欧阳辉祥; 刘细祥; 张金磊; 左卫元

    2014-01-01

    To expand and improve the database of polycyclic aromatic hydrocarbon (PAH) pollution signatures in different environmental samples from sites in China, surface soil samples were collected from five industrial areas of Baise, a prefecture-level city of the Guangxi Zhuang Autonomous Region. The concentration and composition of 16 PAHs listed for prior control by the US EPA were determined using high performance liquid chromatography. Selected diagnostic ratios and principal component analysis were used to identify possible sources of soil PAHs. Concentrations of∑16 PAHs in the present study were shown to vary greatly, and ranged from 18.7 to 6347 μg/kg, depending on the sampling location. The highest concentrations ofΣ16 PAHs were observed in Power plant 2 soils with a value of 1923.4μg/kg. Compared with domestic and foreign research, PAH pollution in the five Baise industrial areas reached medium to high levels. Soil PAH concentrations showed a strong Power plant 2-Power plant 1-Refinery-Lubricants plant-Cement plant gradient. Four-and five-ring PAHs, which have strong carcinogenic mutagenicity and distortion, dominated in the industrial areas with power plants and lubricant plants, while two-and three-ring PAHs dominated the surface soil near cement plants. Among the PAHs detected in the study-area soil, benz[a]anthracene (BaA), benzo[k]fluoranthene (BkF), chrysene (Chr), and fluoranthene (Fla) were the major pollutants occurring above standard levels. The study also suggested that the major sources of soil PAHs in Baise were coal and petroleum combustion (45.0%) and petroleum leakage (18.2%), or a combination of the two (36.8%).%为完善我国实地的不同的PAHs污染特征数据库,系统采集了百色市5个工业区表层土壤样品,利用HPLC分析了16种US EPA 优控 PAHs 的含量和组分特征,运用同分异构体比率法和主成分因子载荷法揭示其污染来源.结果表明,工业区土壤中 PAHs 总含量范围在18

  4. Determination of 15 polycyclic aromatic hydrocarbons in Poyang Lake wetland soil by HPLC%HPLC测定鄱阳湖湿地土壤中15种多环芳烃

    Institute of Scientific and Technical Information of China (English)

    杨平华; 曾祥晖

    2014-01-01

    Determination of polycyclic aromatic hydrocarbons in Poyang Lake wetland soil, by using acetone and hexane(1︰1)as the extraction solvent,extraction of 40min by ultrasonic extraction method, the total amount of solvent is 70 mL (10 g samples), chromatographic conditions: the injection volume was 20μL,flow rate 1 mL/min,temperature 30℃,the appropriate mobile phase gradient elution program and the fluorescence detector wave length conversion program.The concentrations of 15 polycyclic aromatic hydrocarbons in Poyang Lake wetland soil has been determinated by HPLC. The contents of 15 polycyclic aromatic hydrocarbons in Poyang Lake wetland soil is Naphthalene, 92.45;Acenaphthene,not detected;Fluorene, 9.90;Phenanthrene, 91.75;Anthracene,119.67;Fluoranthene,not detected;Pyrene,81.51;Benzo (a) anthracene, 13.26;Chrysene,6.79;Benzo (b) fluoranthene,4.53;Benzo (k) fluoranthene,7.76;Benzo (a) pyrene,not detected;Dibenzo(a,h)anthracene,7.74;Benzo(g,h,i)perylene,not detected;Indeno (123-cd) pyrene,not detected. The standard addition recovery of this method was 76.8%-115.1%, the relative standard deviation (RSD) was 1.3%-5.8%, with good accuracy and precision. The established method can used to determinate the content of polycyclic aromatic hydrocarbons in Poyang Lake wetland soil. It provide the basis for further study of pollution characteristics and source apportionment of polycyclic aromatic hydrocarbons in Poyang Lake wetland soil.%测定鄱阳湖湿地土壤中多环芳烃的含量,采用丙酮+正己烷(1︰1)为提取溶剂,超声提取40 min,总溶剂量为70 mL(10 g样品),色谱条件为进样量为20μL、流量为1 mL/min、柱温30℃,采用适当的流动相梯度淋洗程序与荧光检测器波长变换程序,高效液相色谱法测定鄱阳湖湿地土壤中15种多环芳烃的含量。结果表明:鄱阳湖湿地土壤中15种多环芳烃的含量为(ng/g):萘,92.45;苊,未检出;芴,9.90;菲,91.75;蒽,119

  5. Polycyclic Aromatic Hydrocarbon (pah) In The Bulk Precipitation of The Seine Estuary, France

    Science.gov (United States)

    Motelay-Massei, A.; Ollivon, D.; Garban, B.; Chevreuil, M.

    The evolution of industry and the rising of population have resulted in deep changes in the quality of the environment. Nowadays much more often the attention of analysts is focused on the presence of organic pollutants in precipitation, such as polycyclic aromatic hydrocarbons or pesticides. Atmospheric inputs play a significant role in semivolatile chemicals cycling and alter so the hydrological cycle. PAHs are semi- volatile organic contaminants of great environmental concern because of their car- cinogenic properties. PAHs are produced primarily during incomplete combustion of fossil fuels and wood. Major sources of PAHs to urban atmosphere include au- tomobile traffic, home heating, municipal incinerators and industrial emissions. De- spite their production in urban and industrial sites, PAHs occur at high concentra- tions in rural areas due to their persistence and ability to be transported over long distances. The aim of this investigation was to obtain information about occurrence of organic trace components in precipitation in the Seine Estuary. It was also of in- terest to investigate the spatial and temporal variability of PAHs in the bulk (wet and dry) deposition occurring in the estuary region and to estimate PAH deposition flux on watershed (urban, industrial or rural). Precipitation samples were collected at four locations in the Seine Estuary: the first is an industrial site (Le Havre), two are urban sites (Rouen, representative of urban area influenced by heavy traffic and Notre-Dame de Gravenchon, near from an industrial center) and the last one is ru- ral (Evreux). Each of the sites is located close to a meteorological station. Sam- pling is performed weekly since March 2001. In our analytical conditions, "total PAH" includes 15 compounds: naphthalene (NAP), acenaphtene (ACE), phenanthrene (PHE), anthracene (ANT), fluoranthene (FTH), pyrene (PYR), benzo(a)anthracene (BaA), chrysene (CHR), benzo(b)fluoranthene (BbF), benzo(k)fluoranthene (Bk

  6. 天津西青区不同功能区土壤中多环芳烃分布特征研究%Distribution Characteristics of Polycyclic Aromatic Hydrocarbons in Different Functional Zones of Soils from Xiqing District in Tianjin, China

    Institute of Scientific and Technical Information of China (English)

    王迪; 罗铭; 张茜; 戴礼洪; 刘岩; 王璐; 刘潇威

    2012-01-01

    towns respectively. Not all the 16 PAHs were detected in all 24 samples. Principal component analysis was used to identify the pollution sources of PAHs.The variance contribution rate of top three factors was 91.3%, High-molecular PAHs from burning sources dominated at the first principal component, while, the second principal component mainly attributed to the low molecular PAHs from petroleum pollution sources. Correlation of organic compound with PAHs in soils has also been studied: there existed significant linear correlations between soil organic matters and PAHs(R2=0.613 ) and soil organic matters most closely correlated with chrysen(R2=0.665), indicating that soil organic matter was one of the important factors affecting the PAHs in soil. However, near the serious pollution source of PAHs, the concentration of PAHs in the soils was probably determined by the pollution source and other complicated factors of soils. According to European PAHs risk grading standards, Zhongbei town was moderately polluted, Yangliuqing town and Zhangjiawo town were at light pollution level, Xinkou town was unpolluted.

  7. Geochemical Significance and Distribution Characterisitics of Polycyclic Aromatic Hydrocarbons from the Jurassic Source Rocks in the Heshituoluogai Basin,Northwest Junggar%准噶尔盆地西北部和什托落盖盆地侏罗系烃源岩芳烃分布特征及地球化学意义

    Institute of Scientific and Technical Information of China (English)

    刘洪军; 秦黎明; 张枝焕

    2012-01-01

    研究了准噶尔盆地西北部和什托落盖盆地侏罗系煤系烃源岩多环芳烃的分布规律。结果表明,该区侏罗系烃源岩中多环芳烃分布广泛,两环芳烃至六环芳烃以及七环芳烃均有分布,单体芳烃主要以四环芳烃和五环芳烃的含量较高,其次为两环芳烃和三环芳烃。研究还表明煤和泥岩的多环芳烃分布极易受沉积相差异发生明显变化,比如侏罗系八道湾组泥岩菲、荧蒽、芘、艹屈、苯并荧蒽与苯并[e]芘的丰度均较高,西山窑组泥岩苝的丰度明显偏高于其余化合物;而八道湾组煤中蒽、芘、苯并[a]芴以及苯并荧蒽丰度较高,西山窑组煤中苯并荧蒽、苯并[e]芘和苯并[a]芴的丰度偏高。另外煤的萘与二苯并噻吩成熟度参数值明显高于泥岩,并且与Pr/Ph值和δ13Caro值呈正相关,与四环芳烃和五环芳烃参数值呈负相关,进一步研究表明多环芳烃比值极易受到有机相类型差异分布影响,仅菲的参数值差异小,泥岩RC值与实测RO值相近,二苯并噻吩/菲值与Pr/Ph值关系和OF/(OF+F)值与SF/(SF+F)值关系反映了侏罗系浅湖相至河流相或三角洲相为开阔水体的弱氧化—强氧化沉积环境。%According to the GC-MS analysis and identification of aromatic hydrocarbon,the distribution of aromatic hydrocarbons is investigated.The results indicate that the distribution of aromatic hydrocarbons is extensive from dinuclear aromatics to heptacyclic aromatics.The relative abundance of tetracyclic and pentacyclic aromatics is apparently higher than that of dinuclear and tricyclic aromatics in Jurassic source rocks.The distribution of PAH in mudstone and coal is easily affected by the sedimentary facies.The relative content of phenanthrene,fluoranthene,pyrene,chrysene,benzofluoranthene and benzo[e]pyrene is higher than other compounds in the mudstone from Badaowan Formation,but in Xishanyao Formation,the content of perylene is

  8. Laboratory and Ambient Studies of the Products of Gas-Phase Hydroxyl and Nitrate Ion Radical-Initiated Reactions with Selected PAHs

    Science.gov (United States)

    Zimmermann, Kathryn Jean

    Nitrated polycyclic aromatic hydrocarbon (nitro-PAH) product distributions from the gas-phase hydroxyl (OH) and nitrate (NO3) radical-initiated reactions with selected PAHs, as well as the heterogeneous reactions of surface-bound PAHs with N2O5 and HNO3, were investigated. Chapter 2 presents formation yields of nitro-PAHs from the gas-phase OH radical-initiated reactions of 1,7- and 2,7-dimethylnaphthalene (DMN) as a function of NO 2 concentration over the range 0.04-0.14 ppmv. The measured formation yields of dimethylnitronaphthalenes (DMNNs) under conditions that the OH-DMN adducts reacted solely with NO2 were 0.252 ± 0.094% for Σ1,7-DMNNs and 0.010 ± 0.005% for Σ2,7-DMNNs. 1,7-dimethyl-5-nitronaphthalene (1,7DM5NN) was the major nitro-isomer formed, with a limiting high-NO 2 concentration yield of 0.212 ± 0.080% and with equal reactions of the 1,7-DMN-OH adduct with NO2 and O2 occurring in air at 60 ± 39 ppbv of NO2, indicating that the OH-DMN adduct reaction with NO2 can be important at NO2 concentrations commonly found in urban atmospheres. Although the yields of the DMNNs are low, ≤0.3%, the DMNN (and ethylnitronaphthalene) profiles from chamber experiments match well with those observed in polluted urban areas under conditions where OH radical-initiated chemistry is dominant, such as Mexico City, Mexico. Chapter 3 examines the nitro-PAH products of gas-phase OH and NO 3 radicals and heterogeneous N2O5 reactions with fluoranthene, pyrene, benz[a]anthracene, chrysene, and triphenylene. Analysis of nitro-PAHs in the NIST diesel particulate SRM (1975) and selected ambient samples are also presented. 2-Nitrofluoranthene (2-NFL) was the most abundant nitro-PAH in Riverside, CA and Mexico City, and the mw 273 nitro-PAHs were observed in lower concentrations. However, in Tokyo, Japan, concentrations of 1- + 2-nitrotriphenylene (NTP) were more similar to those of 2-NFL. Comparing specific nitro-PAH ratios in ambient particulate samples from Tokyo, Mexico City

  9. Charakterisierung von Sulfotransferasen im Gastrointestinaltrakt von Mensch und Ratte und Aktivierung von Promutagenen in V79-Zellen, die eine intestinale Form (1B1) des Menschen und der Ratte exprimieren

    Science.gov (United States)

    Teubner, Wera

    2001-05-01

    keine weiteren Zellteilungen mehr durch. Daher sind DNA-Schäden in diesen Zellen ein sehr geringes Risiko für den Organismus. Soweit die reaktiven Metabolite in diesen Zellen gefangen bleiben, kann die Bioaktivierung in diesen Zellen und die Bildung von Addukten als protektiv betrachten werden, da letztere nach wenigen Tagen mit den toten Zellen in das Darmlumen abgegeben werden. Für den Vergleich der Bioaktiverung von Promutagenen durch die Form 1B1 des Menschen und der Ratte wurden aus V79 Lungenfibroblasten des Chinesischen Hamsters abgeleitete Zellinien hergestellt, die je eine der beiden Formen stabil exprimieren. Damit standen 1B1-profiziente Indikatorzellen für den HPRT-Genmutationstest zur Verfügung, und die 1B1-abhängige Bioaktivierung konnte in einem System untersucht werden, die dem eukaryontischen Organismus näher steht als die für die Ames-Tests verwendeten Bakterien. So war z.B. die Sulfotransferase wie im Gewebe im Zytoplasma lokalisiert. Als Modellsubstanzen wurden hierbei die bereits in TA1538-h1B1 mutagen wirkenden benzylischen Alkohole 6-Hydroxymethylbenzo[a]pyren und 4-Hydroxycyclopenta-[def]chrysen getestet. Da die Sensitivität einer Sulfotransferase-exprimierenden V79-Zellinie sowohl durch die Menge an Sulfotransferase als auch durch die Verfügbarkeit des Sulfodonors limitiert sein könnte, wurden die Mutagenitätsexperimente mit V79-r1B1-Zellinien durchgeführt, die sich in ihrer Enzymaktivität um das Zwanzigfache unterschieden: V79-r1B1/A und -/B. Eine starke Erhöhung der Mutantenfrequenz wurde nur in der hoch exprimierenden Zellinie V79-r1B1/A (1019 ± 224 pmol/mg/min) beobachtet, so da eine gravierende Beeinträchtigung der Sensitivität durch einen Mangel an Kosubstrat ausgeschlossen wurde. In der niedriger exprimierenden Zellinie V79-r1B1/B (57 ± 9 pmol/mg/min) war nur mit 6-Hydroxymethylbenzo[a]pyren ein schwacher Anstieg der Mutantenfrequenz zu erkennen, der mit 0,3 µM bei einer in etwa 100fach höheren Konzentration begann