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Sample records for aliphatic hydrocarbons polycyclic

  1. The effect of aliphatic fuel constituents on the biodegradation of polycyclic aromatic hydrocarbons

    SciTech Connect

    Gamerdinger, A.P.

    1995-12-01

    In petroleum-derived waste, n-alkanes are often codeposited with polycyclic aromatic hydrocarbons (PAHs). The impact of aliphatic fuel constituents on the biodegradation of the more toxic PAHs is considered. Biodegradation of naphthalene by a Coryneform bacteria was examined in biphasic, slurry systems containing and aliphatic solvent in addition to the aqueous phase. The effect of solvent hydrophobicity was evaluated by varying the solvent treatment; a homologous series of n-alkanes was used. Relative to an aqueous system (no solvent), the extent of naphthalene degradation was enhanced in the presence of decane, dodecane, and hexadecane. Biodegradation was apparent, but decreased in the presence of octane, and was completely absent in the presence of hexane. The impact of aliphatic constituents on PAH biodegradation is a function of solvent hydrophobicity. The results indicate that the presence of multiple chemical constituents in complex systems modifies bioavailability and biodegradation.

  2. A THEORETICAL STUDY ON THE VIBRATIONAL SPECTRA OF POLYCYCLIC AROMATIC HYDROCARBON MOLECULES WITH ALIPHATIC SIDEGROUPS

    SciTech Connect

    Sadjadi, SeyedAbdolreza; Zhang, Yong; Kwok, Sun

    2015-03-01

    The role of aliphatic side groups in the formation of astronomical unidentified infrared emission (UIE) features is investigated by applying the density functional theory to a series of molecules with mixed aliphatic-aromatic structures. The effects of introducing various aliphatic groups to a fixed polycyclic aromatic hydrocarbon (PAH) core (ovalene) are studied. Simulated spectra for each molecule are produced by applying a Drude profile at T = 500 K while the molecule is kept at its electronic ground state. The vibrational normal modes are classified using a semi-quantitative method. This allows us to separate the aromatic and aliphatic vibrations, and therefore provides clues to what types of vibrations are responsible for the emissions bands at different wavelengths. We find that many of the UIE bands are not pure aromatic vibrational bands but may represent coupled vibrational modes. The effects of aliphatic groups on the formation of the 8 μm plateau are quantitatively determined. The vibrational motions of methyl (–CH{sub 3}) and methylene (–CH{sub 2} –) groups can cause the merging of the vibrational bands of the parent PAH and the forming of broad features. These results suggest that aliphatic structures can play an important role in the UIE phenomenon.

  3. Aliphatic and polycyclic aromatic hydrocarbons in the surface sediments of the Mediterranean: assessment and source recognition of petroleum hydrocarbons.

    PubMed

    El Nemr, Ahmed; El-Sadaawy, Manal M; Khaled, Azza; Draz, Suzanne O

    2013-06-01

    Coastal marine sediment samples were collected from ten sampling stations along the Egyptian Mediterranean coast in April 2010. All sediment samples were analyzed for aliphatic (C7 to C34) and polycyclic aromatic hydrocarbons (PAHs) as well as total organic carbon (TOC) contents and grain size analysis. Total aliphatic hydrocarbons ranged from 1621.82 to 9069.99 ng/g (dry weight), while aromatic hydrocarbons (16 PAHs) varied between 208.69 and 1020.02 ng/g with an average of 530.68 ± 225.86 ng/g dwt. Good correlations observed between certain PAH concentrations allowed to identify its origin. The average TOC percent was varied from 0.13 to 1.46 %. Principal component analysis was used to determine the sources of hydrocarbon pollutants in sediments of Mediterranean. Additionally, special PAHs compound ratios suggest the petrogenic origins.

  4. Aliphatic and polycyclic aromatic hydrocarbons in sediments of Kaohsiung Harbour and Adjacent Coast, Taiwan.

    PubMed

    Lee, Chon-Lin; Hsieh, Ming-Tsuen; Fang, Meng-Der

    2005-01-01

    Surficial sediment samples collected from Kaohsiung Harbour and its nearby coast were analyzed for aliphatic hydrocarbons and parent polycyclic aromatic hydrocarbons (PAHs). According to our results, the average total concentrations of n-alkanes (n-C12 to C35) and aromatics (15 PAHs) were 4.33 microg g(-1) dry weight (ranged 0.46-22.60) and 0.59 microg g(-1) dry weight (ranged 0.09-1.75), respectively. The highest concentrations of aliphatic and aromatic hydrocarbons were recorded in stations near the estuaries of Qianzhen River and Love River, respectively. Aliphatic hydrocarbons in the samples indicate that there has been significant non-petrogenic, possibly terrestrial, contribution in the sediment of the open coast of Kaohsiung Harbour and that there has been dominant contribution from petrogenic sources in the sediment of the inner harbour. PAHs, detected in the samples, however, indicated a higher pyrolytic contribution in open-coast samples and a higher petrogenic contribution in the inner harbour. Overall, sediment concentrations of total alkanes in this study were comparable to those found in Victoria Harbour, Hong Kong and are higher than those found in Xiamen Harbour, China. Concentrations of total PAHs in inner Kaohsiung Harbour sediments were relatively lower than those found in Victoria Harbour, Hong Kong and Xiamen Harbour, China, but comparable to those found in Hsin-ta Harbour, Taiwan and Incheon Harbour, Korea. In comparison with several effect-based sediment quality guidelines, most PAH concentrations found in samples taken from inner harbour stations exceeded the Threshold Effect Level of Florida indicating a slight possibility of adverse effects.

  5. Aliphatic and polycyclic aromatic hydrocarbons characterisation of Coimbra and Oporto PM2.5 urban aerosol

    NASA Astrophysics Data System (ADS)

    Rocha, A. C.; Mirante, F.; Gonçalves, C.; Nunes, T.; Alves, C.; Evtyugina, M.; Kowacz, M.; Pio, C.; Rocha, C.; Vasconcelos, T.

    2009-04-01

    The concentration of organic pollutants in urban areas is mostly due to incomplete combustion from vehicles, industries and domestic heating. Some of these compounds, principally the aliphatic (ALIPH) and polycyclic aromatic hydrocarbons (PAHs) promote harmful effects in human health. The determination of the ALIPH and PAHs concentration levels and their possible emission sources are useful for air quality management and source apportionment studies. In order to estimate and compare the ambient concentrations and establish the main sources of these compounds, the fine fraction of the atmospheric particulate matter (PM2.5) was collected simultaneously in Oporto and Coimbra during summer and winter seasons using a high volume sampler. The organic compounds were extracted from the particulate matter, under reflux with dichloromethane and the total organic extract (TOE) was fractionated by flash chromatography using five different eluents with increasing polarity. The hydrocarbon fractions were analysed by gas chromatography/mass spectrometry (GC/MS). Here we present and discuss the qualitative and quantitative composition of the aliphatic and aromatic fractions present in PM2.5 samples from both cities. The homologous series of C14 to C34 n-alkanes, isoprenoid hydrocarbons (pristane and phytane), PAHs and some petroleum markers have been identified and quantified. With the purpose of identifying the possible sources, various molecular diagnostic ratios were calculated. The global carbon preference index (CPI) closer to the unity, the large concentration of the unresolved complex mixture (UCM) and the presence of PAHs indicate that motor vehicle exhaust was the main emission source of the aliphatic and polycyclic aromatic fractions of Oporto and Coimbra aerosol, especially in the first city. Also, the remarkable presence of petroleum biomarkers such, as hopanes, confirms the previous results. Concentration ratios between PAHs were calculated and used to assign emission

  6. Distribution of aliphatic hydrocarbons, polycyclic aromatic hydrocarbons and organochlorinated pollutants in deep-sea sediments of the Southern Cretan margin, Eastern Mediterranean Sea: a baseline assessment.

    PubMed

    Mandalakis, Manolis; Polymenakou, Paraskevi N; Tselepides, Anastasios; Lampadariou, Nikolaos

    2014-07-01

    Deep sediments from the southern Cretan margin were analyzed to establish baseline levels for various types of organic pollutants before the anticipated intensification of anthropogenic activities. The total concentration of aliphatic hydrocarbons (ΣAH:326-3758ngg(-1), dry weight) was similar to those reported for deep sediments of the western Mediterranean Sea, while considerably lower levels were measured for polycyclic aromatic hydrocarbons (ΣPAH:9-60ngg(-1)). Source-diagnostic ratios suggested that the aliphatic hydrocarbons in sediments were mainly of terrestrial biogenic origin, while polycyclic aromatic hydrocarbons stemmed from the deposition of long-range transported combustion aerosols. Among the organochlorinated compounds analyzed, β-hexachlorocyclohexane (β-HCH:222-7052pgg(-1)), 1,1,1-trichloro-2,2-bis(4-chlorophenyl)ethane (p,p'-DDT:37-2236pgg(-1)) and polychlorinated biphenyls (ΣPCB:38-1182pgg(-1)) showed the highest abundance in sediments. The presence of HCHs and PCBs was attributed to historical inputs that have undergone extensive weathering, whereas an ongoing fresh input was suggested for p,p'-DDT. Multiple linear regression analysis revealed that the levels of the various pollutants in sediments were controlled by different factors, but with organic carbon content playing a prominent role in most cases.

  7. {Polycyclic aromatic hydrocarbons (PAHs) and aliphatic hydrocarbons in gas and particle phases in two sites of Mexico: MILAGRO project}

    NASA Astrophysics Data System (ADS)

    Amador-Muñoz, O.; Villalobos-Pietrini, R.; Castro, T.; Gaspariano-Larino, R.

    2009-04-01

    Aliphatic hydrocarbons are markers of anthropogenic and biogenic emission sources1; meanwhile PAHs are generated by incomplete combustion sources2. The last ones are important compounds due to their carcinogenic and mutagenic properties3,4. The aim of this study was to identify and quantify aliphatic hydrocarbons and PAHs in gas and particles phases of the atmospheric aerosol and to determine the day and night time behavior during the MILAGRO (Megacity Initiative: Local Global and Research Observations) campaign. The gas phase was collected on polyurethane foam, while particles less than 2.5 m (PM2.5) were collected on glass fiber filters covered with Teflon (TIGF, pallflex) of 8x10 in. Samplings were carried out with a high volume sampler (Tisch) with a flow of 1.13 m3 min-1 at two sites: Instituto Mexicano del Petróleo (T0) and Tecamac (T1) located at North and Northeast of Mexico City, respectively during day (7:00 am-7:00 pm) and night time (7:00 pm-7:00 am) from 1 to 29 of March, 2006. Ninteen PAHs and 23 aliphatic hydrocarbons from n-C13H28 to n-C35H72 were analyzed by gas chromatography coupled to mass spectrometry in impact mode. The samples were spiked with deuterads PAHs and aliphatics hydrocarbons before ultrasound extraction. Medians comparisons were made with Mann-Whitney U test. PAHs with molecular weight (MW) less than 228 g mol-1 were distributed in the gas phase, in both sites. Higher concentrations of PAHs ≥ 228 g mol-1 in PM2.5, were observed during night period (p

  8. Polycyclic Aromatic Hydrocarbons with Aliphatic Sidegroups: Intensity Scaling for the C–H Stretching Modes and Astrophysical Implications

    NASA Astrophysics Data System (ADS)

    Yang, X. J.; Li, Aigen; Glaser, R.; Zhong, J. X.

    2017-03-01

    The so-called unidentified infrared emission (UIE) features at 3.3, 6.2, 7.7, 8.6, and 11.3 μ {{m}} ubiquitously seen in a wide variety of astrophysical regions are generally attributed to polycyclic aromatic hydrocarbon (PAH) molecules. Astronomical PAHs may have an aliphatic component, as revealed by the detection in many UIE sources of the aliphatic C–H stretching feature at 3.4 μ {{m}}. The ratio of the observed intensity of the 3.4 μ {{m}} feature to that of the 3.3 μ {{m}} aromatic C–H feature allows one to estimate the aliphatic fraction of the UIE carriers. This requires knowledge of the intrinsic oscillator strengths of the 3.3 μ {{m}} aromatic C–H stretch ({A}3.3) and the 3.4 μ {{m}} aliphatic C–H stretch ({A}3.4). Lacking experimental data on {A}3.3 and {A}3.4 for the UIE candidate materials, one often has to rely on quantum-chemical computations. Although the second-order Møller–Plesset (MP2) perturbation theory with a large basis set is more accurate than the B3LYP density functional theory, MP2 is computationally very demanding and impractical for large molecules. Based on methylated PAHs, we show here that, by scaling the band strengths computed at an inexpensive level (e.g., B3LYP/6-31G*), we are able to obtain band strengths as accurate as those computed at far more expensive levels (e.g., MP2/6-311+G(3df,3pd)). We calculate the model spectra of methylated PAHs and their cations excited by starlight of different spectral shapes and intensities. We find that {({I}3.4/{I}3.3)}{mod}, the ratio of the model intensity of the 3.4 μ {{m}} feature to that of the 3.3 μ {{m}} feature, is insensitive to the spectral shape and intensity of the exciting starlight. We derive a straightforward relation for determining the aliphatic fraction of the UIE carriers (i.e., the ratio of the number of C atoms in aliphatic units {N}{{C},{ali}} to that in aromatic rings {N}{{C},{aro}}) from the observed band ratios {({I}3.4/{I}3.3)}{obs}: {N

  9. Presence of aliphatic and polycyclic aromatic hydrocarbons in near-surface sediments of an oil spill area in Bohai Sea.

    PubMed

    Li, Shuanglin; Zhang, Shengyin; Dong, Heping; Zhao, Qingfang; Cao, Chunhui

    2015-11-15

    In order to determine the source of organic matter and the fingerprint of the oil components, 50 samples collected from the near-surface sediments of the oil spill area in Bohai Sea, China, were analyzed for grain size, total organic carbon, aliphatic hydrocarbons (AHs), and polycyclic aromatic hydrocarbons (PAHs). The concentrations of C15-35 n-alkanes and 16 United States Environmental Protection Agency (US EPA) priority pollutant PAHs were found in the ranges of 0.88-3.48μg g(-1) and 9.97-490.13ng/g, respectively. The terrestrial organic matters characterized by C27-C35 n-alkanes and PAHs, resulting from the combustion of higher plants, are dominantly contributed from the transportation of these plants by rivers. Marine organic matters produced from plankton and aquatic plants were represented by C17-C26 n-alkanes in AHs. Crude oil, characterized by C17-C21 n-alkanes, unresolved complex mixture (UCM) with a mean response factor of C19 n-alkanes, low levels of perylene, and a high InP/(InP+BghiP) ratio, seeped into the oceans from deep hydrocarbon reservoirs, as a result of geological faults.

  10. Organic composition of atmospheric urban aerosol: Variations and sources of aliphatic and polycyclic aromatic hydrocarbons

    NASA Astrophysics Data System (ADS)

    Mazquiarán, Miguel A. Barrero; Cantón Ortiz de Pinedo, Lourdes

    2007-09-01

    The non-polar organic composition of airborne particulate matter was analysed over a two year period in an urban area under oceanic climate conditions (Errenteria, Basque Country, Spain). In addition, the distribution of polycyclic aromatic hydrocarbons (PAH) among different aerosol particle sizes was determined. Clues as to the origin of various particle types were gained by using scanning electron microscopy to view the morphology of the particulates in each size fraction. Samples were collected on glass fibre filters and analysed by means of soxhlet extraction and gas chromatography (either with a flame ionization detector or coupled to a mass spectrometry). In general, total PAH levels were moderate (0.96-50 ng m - 3 ) as compared to other studies conducted in Europe, and showed clear seasonal variation with maxima in winter and minima in summer. Vehicular traffic was identified as a major source of PAHs in the study area. Regarding particle size, a bimodal distribution was observed. The large sized particles exhibited an apparent seasonal variation with higher concentrations in winter than in summer. The dependences between particle size, PAH distribution and meteorological variables were studied with multivariate statistics. Three main sources of organic compounds were identified: combustion, vegetation, and atmospheric oxidation.

  11. Distribution of trace metals, aliphatic hydrocarbons and polycyclic aromatic hydrocarbons in sediment cores from the Sicily Channel and the gulf of Tunis (south-western Mediterranean Sea).

    PubMed

    Mzoughi, Nadia; Chouba, Lassaad

    2011-01-01

    Under the framework of the IAEA's Technical Co-operation project RAF7/004, international research cruises were carried out in 2004 to assess the distribution of radionuclides and micropollutants in the south-western Mediterranean Sea. Sediments samples had variable concentrations of total aliphatic hydrocarbons and polycyclic aromatic hydrocarbons ranging from 0.2 to 1.8 microg g(-1) and 26.9 to 364.4 ng g(-1), respectively, in the Sicily Channel and from 0.7 to 2.8 microg g(-1) and 14.7 to 618.1 ng g(-1), respectively, in the open sea of the Gulf of Tunis. Hydrocarbon concentrations changed with depth and were relatively high at 3 cm and 10 cm depths. The use of 'fingerprint' ratios of certain isomeric pairs of polycyclic aromatic hydrocarbons (PAH) and the proportion of 2-3 ring and 4-5 ring PAH concentrations showed that the main origins are characteristic of petroleum sources. The ranges of trace metal concentrations, expressed in microgg(-1), in the Sicily Channel and in the Gulf of Tunis, respectively, were: Hg 0.009-0.2 and 0.02-0.1; Pb 9.9-26.1 and 21.2-32.5; Cd 0.06-0.1 and 0.07-0.33; Fe 23.7-28.1 and 29.9-36.2p; Zn 83-99.5 and 83-104; Mn 309.2-752.5 and 651-814; Cu 17.1-18.5 and 33.5-51.3. Sediment metal abundances were in the order: Mn > Zn > Fe > Cu > Pb > Cd > Hg. The results showed significant differences (p < 0.001) for trace metal and hydrocarbon mean concentrations between the two cores. These concentrations are generally similar to the background levels from the Mediterranean Sea and could be affected by physico-chemical conditions and sedimentation rate as well as biodegradation.

  12. Patterns and sources of particle-phase aliphatic and polycyclic aromatic hydrocarbons in urban and rural sites of western Greece

    NASA Astrophysics Data System (ADS)

    Kalaitzoglou, Maria; Terzi, Eleni; Samara, Constantini

    Particle-bound aliphatic and polycyclic aromatic hydrocarbons (AHs and PAHs, respectively) were determined in the ambient air of the Eordea basin, in western Greece, where intensive coal burning for power generation takes place. Thirteen PAHs, n-alkanes (C 14-C 35), hopanes, and isoprenoid hydrocarbons (pristane and phytane) were determined in the total suspended particles collected from the atmosphere of four sites within the basin receiving potential impacts from various sources, such as fly ash, coal mining, automobile traffic, domestic heating, and agricultural or refuse burning. The same organic species were also determined in the fly ash generated in power stations, and in particulate emissions from open burning of biomass (dry corn leaves) and refuse burning. Organic particle sources were resolved using concentration diagnostic ratios and factor analysis (FA). A multivariate statistical receptor model (Absolute Principal Component Analysis, APCA) was finally employed to estimate the contribution of identified sources to the measured concentrations of organic pollutants. Four major sources for ambient PAHs and AHs were identified displaying variable contribution in different sites: (a) fossil fuel combustion, (b) biogenic emissions, (c) refuse burning, and (d) oil residues. Fuel combustion was the major source of ambient PAHs and an important source of n-alkanes in the range C 21-C 28. Oil residues were found to be the major source of low molecular weight n-alkanes (particularly the C 14-C 16), and an important source of pristane, phytane and UCM. Biogenic sources were primarily responsible for the high molecular weight n-alkanes explaining almost the entire concentration levels of homologues >C 32. Biomass burning was particularly important for the C 23-C 26n-alkanes. Despite the vicinity of certain sampling sites to power stations, coal fly ash was not identifiable as a source for ambient PAHs and AHs.

  13. Isolation, characterization of Rhodococcus sp. P14 capable of degrading high-molecular-weight polycyclic aromatic hydrocarbons and aliphatic hydrocarbons.

    PubMed

    Song, Xiaohui; Xu, Yan; Li, Gangmin; Zhang, Ying; Huang, Tongwang; Hu, Zhong

    2011-10-01

    Rhodococcus sp. P14 was isolated from crude oil-contaminated sediments. This strain was capable of utilizing three to five rings polycyclic aromatic hydrocarbons (PAHs) including phenanthrene (Phe), pyrene (Pyr), and benzo[a]pyrene (BaP) as a sole carbon and energy source. After cultivated with 50mg/L of each PAH, strain P14 removed 43% Phe, 34% Pyr and 30% BaP in 30 d. Four different hydroxyphenanthrene products derived from Phe by strain P14 (1,2,3,4-hydroxyphenanthrene) were detected using SPME-GC-MS. Strain P14 also was capable of degrading mineral oil with n-alkanes of C17 to C21 carbon chain length. Compared with glucose-grown cells, PAHs-grown cells had decreased contents of shorter-chain length fatty acids (≤ C16:0), increased contents of C18:0, Me-C19:0 and disappeared odd-number carbon chain fatty acids. The contents of unsaturated C19:1, Me-C19:0 increased and C18:0 decreased in mineral oil-grown cells. At the same time, the strain P14 tended to float when cultivated in mineral oil-supplemented liquid medium. The degradation capability of P14 to alkane and PAHs and its floating characteristics will be very helpful for future's application in oil-spill bioremediation.

  14. Flux of aliphatic and polycyclic aromatic hydrocarbons to Central Puget Sound from Seattle (Westpoint) primary sewage effluent

    SciTech Connect

    Barrick, R.C.

    1982-10-01

    Concentrations and mass emission rates are reported for hydrocarbons in a 20-month evaluation of primary municipal waste water discharging to marine waters of Puget Sound from Seattle, WA. On the average, METRO (Westpoint) discharges 475 metric tons/year of aliphatic hydrocarbons and approximately 1 metric ton/year of 3-7 ring polynuclear aromatic hydrocarbons (PAH), corresponding to discharges of 2.6 and 0.005 g/(capita day), respectively. Effluent PAH containing greater than or equal to 4 rings apparently derive principally from storm-water contributions. A comparison of METRO's yearly average discharge of different hydrocarbon components with observed hydrocarbon fluxes in adjacent Puget Sound surface sediments suggests negligible accumulations of the resolvable alkanes (derived from the effluent), partial accumulations of an unresolved complex mixture and phenanthrene, and substantial accumulations of the greater than or equal to4-ring PAH. The discharge accounts for a major portion of the sedimentary aliphatic fossil hydrocarbon flux and is one of several important PAH contributors. 45 references, 2 figures, 5 tables.

  15. Sources, distribution, and water column processes of aliphatic and polycyclic aromatic hydrocarbons in the northwestern Black Sea water

    SciTech Connect

    Maldonado, C.; Bayona, J.M.; Bodineau, L.

    1999-08-15

    Aliphatic and aromatic hydrocarbons have been determined in suspended particulate matter collected at subsurficial seawater and three vertical profiles in a transect from the continental shelf, slope, and deep basin of the western Black Sea. The dissolved phase was collected at subsurficial and in the redoxcline. The highest concentrations of hydrocarbons were detected in the Danube, Dnieper, and Dniester River Estuaries and other point sources of pollution located offshore Romania and Bulgaria where oil production and refining is carried out. Concentrations of hydrocarbons decreased with increasing distance from the coast, but relatively high concentrations were found at the open stations where the particulate organic carbon (POC) is higher. Fossil PAHs are predominant in the coastal stations, and the unresolved complex mixture (UCM) of aliphatic hydrocarbons is predominantly of a fossil common origin according to the hopane and sterane distribution. The fossil to pyrolytic PAH ratio decreases with source distance attributable to a deposition of pyrolytic PAHs. The spatial distribution of PAHs found in the dissolved phase is evenly distributed. The unresolved complex mixture/alkane ratio is higher in the dissolved phase and can be attributable to a faster degradation of labile n-alkanes in this phase. Vertical profiles of hydrocarbons in suspended particles show two submaxima located in the biomass maximum abundance and at the redoxcline where there is an enrichment referred to POC due to phytoplankton or bacteria uptake, respectively.

  16. [Mutagenicity of mixtures of halogenated aliphatic hydrocarbons and polycyclic aromatic hydrocarbons in the Ames test with TA98 and TA100].

    PubMed

    Kevekordes, S; Porzig, J; Gebel, T; Dunkelberg, H

    1998-02-01

    Within the framework of the assessment of the genotoxic potential of environment samples the Salmonella-microsome-test (Ames-test) is often used as a screening-test. It is one of the most applied biotest systems and possesses a large scientific acceptance. Because most environment samples are mixtures of various substances, possible effects resulting from the combination should be taken into account with regard to the mutagenic potential. In this context we investigated eight polycyclic aromatic hydrocarbons each combined with six halogenated aliphatic hydrocarbons as to their mutagenicity in the Salmonella-microsome-test with TA98 and TA100. For an exogenous metabolizing system, Arochlor 1254 induced rat liver S9-mix was used. Benz-a-pyrene in combination with bromodichloromethane (Ames neg. in TA98 and TA100 +S9) showed an increase in the number of the revertants up to 25% in TA98 and TA100 (+S9). Carbon tetrachloride (Ames neg. in TA98 and TA100 +S9) showed in TA100 (+S9) an increase in the number of the revertants of 18% at most. In the combination 3-methylcholanthrene with dichloromethane the number of revertants in TA98 (+S9) increased by 25% and in TA100 (+S9) by 18%. Hexachloroethane (weakly mutagenic in TA98 +S9) in combination showed in TA98 (+S9) a slightly increased number of revertants with benz-a-pyrene as well with 3-methylcholanthrene. All the other substances tested (chrysene, phenanthrene, anthanthrene, dibenz-a, i-pyrene, triphenylene, fluoranthene) in combination with either tetrachloroethylene or trichloroethene did not cause an increase in mutagenicity.

  17. The C-H Stretching Features at 3.2--3.5 μm of Polycyclic Aromatic Hydrocarbons with Aliphatic Sidegroups

    NASA Astrophysics Data System (ADS)

    Yang, X. J.; Li, Aigen; Glaser, R.; Zhong, J. X.

    2016-07-01

    The so-called “unidentified” infrared emission (UIE) features at 3.3, 6.2, 7.7, 8.6, and 11.3 μm are ubiquitously seen in a wide variety of astrophysical regions. The UIE features are characteristic of the stretching and bending vibrations of aromatic hydrocarbon materials, e.g., polycyclic aromatic hydrocarbon (PAH) molecules. The 3.3 μm aromatic C-H stretching feature is often accompanied by a weaker feature at 3.4 μm. The latter is generally thought to result from the C-H stretch of aliphatic groups attached to the aromatic systems. The ratio of the observed intensity of the 3.3 μm aromatic C-H feature to that of the 3.4 μm aliphatic C-H feature allows one to estimate the aliphatic fraction of the UIE carriers, provided that the intrinsic oscillator strengths of the 3.3 μm aromatic C-H stretch ({A}3.3) and the 3.4 μm aliphatic C-H stretch ({A}3.4) are known. While previous studies on the aliphatic fraction of the UIE carriers were mostly based on the {A}3.4/{A}3.3 ratios derived from the mono-methyl derivatives of small PAH molecules, in this work we employ density functional theory to compute the infrared vibrational spectra of PAH molecules with a wide range of sidegroups including ethyl, propyl, butyl, and several unsaturated alkyl chains, as well as all the isomers of dimethyl-substituted pyrene. We find that, except for PAHs with unsaturated alkyl chains, the corresponding {A}3.4/{A}3.3 ratios are close to that of mono-methyl PAHs. This confirms the predominantly aromatic nature of the UIE carriers previously inferred from the {A}3.4/{A}3.3 ratio derived from mono-methyl PAHs.

  18. Aliphatic hydrocarbons of the fungi.

    NASA Technical Reports Server (NTRS)

    Weete, J. D.

    1972-01-01

    Review of studies of aliphatic hydrocarbons which have been recently detected in the spores of phytopathogenic fungi, and are found to be structurally very similar to the alkanes of higher plants. It appears that the hydrocarbon components of the few mycelial and yeast forms reported resemble the distribution found in bacteria. The occurence and distribution of these compounds in the fungi is discussed. Suggested functional roles of fungal spore alkanes are presented.

  19. Polycyclic aromatic hydrocarbons, aliphatic hydrocarbons, trace elements and monooxygenase activity in birds nesting on the North Platte River, Casper, Wyoming, USA

    USGS Publications Warehouse

    Custer, T.W.; Custer, Christine M.; Dickerson, K.; Allen, K.; Melancon, M.J.; Schmidt, L.J.

    2001-01-01

    Tree swallow (Tachycineta bicolor) and house wren (Troglodytes aedon) eggs and chicks were collected near a refinery site on the North Platte River, Casper, Wyoming, USA and at a reference site 10 km upstream. Total polycylic aromatic hydrocarbon (PAH) concentrations in swallow and wren chicks were higher at the refinery site than at the reference site. Polycylic aromatic hydrocarbon concentrations in sediment and chick dietary samples were consistent with these findings. The general lack of methylated PAHs in sediment, diet, and bird carcasses suggested that the PAHs were derived from combustion and not from petroleum. The predominance of odd numbered aliphatic hydrocarbons and the low ratios (≤ 0.25) of pristane: n-C17 and phytane: n-C18 in chick and diet samples also suggested that swallow and wren chicks were not being chronically exposed to petroleum. Mean ethoxyresorufin-O-dealkylase and benzyloxyresorufin-O-dealkylase activities in tree swallow livers averaged nine times higher at the refinery site than at the reference site and were probably induced by exposure to PAHs. Trace element concentrations in eggs and livers of swallows and wrens were similar or greater at the reference site than at the refinery site. Selenium, strontium, and boron concentrations were elevated in eggs and livers of swallows and wrens at both the refinery and reference sites.

  20. Aliphatic and polycyclic aromatic hydrocarbons (PAHs) in soils of the northwest Qinling Mountains: Patterns, potential risk and an appraisal of the PAH ratios to infer their source.

    PubMed

    Liu, Yanhong; Wu, Yingqin; Xia, Yanqing; Lei, Tianzhu; Tian, Chuntao; Hou, Xiaohuan

    2017-03-21

    Surface soils from the tourist areas of the northwest Qinling Mountains were analyzed to determine the concentrations, probable sources and potential risks of hydrocarbons. Concentrations of aliphatic and aromatic hydrocarbons ranged from 4.18 to 3240 ng g(-1) and 0.0462 to 101 ng g(-1) dry weight, respectively. The extent of soil contamination by hydrocarbons was generally typified by unpolluted to slightly polluted levels. The incremental lifetime cancer risks (ILCRs) for exposure to soil-borne PAHs indicated complete safety for tourists. Early diagenesis of natural products, bacteria activities and petroleum were the three main sources of aliphatic hydrocarbons, while the transport of air pollutants from pyrolytic processes was the main origin of PAHs. Because the photochemical reaction of PAHs in the atmosphere would produce lower ratios for Ant/(Ant + Phe), BaA/(BaA + Chr) and IcdP/(IcdP + BghiP), but a higher ratio for Fla/(Fla + Pyr), the source classification highly depended on the diagnostic ratios chosen. The plot of ΣCOM/Σ13PAH vs. ΣLMW/ΣHMWPAH provide additional information to distinguish the origins of PAHs, and it showed a cluster of pyrogenic sources except for sample JFS-8. Four sources were resolved by principal component analysis: (1) a low temperature pyrogenic process related to the use of fossil fuel and biomass, such as charcoal, straw and wood, which contributes 63.1% of the measured PAHs; (2) the potential contribution of diagenetic processes, contributing 18.4%; (3) traffic emissions, contributing 9.27%; and (4) bioconversion/bacterial action, contributing 5.82%. Additionally, there was a good exponential relationship (r(2) = 0.969) between the natural n-alkanes ratio (NAR) and carbon preference index for C23-C35 (CPI23-35) for all samples, which is of great use for the determination of the origins of aliphatic hydrocarbon.

  1. Aliphatic and polycyclic aromatic hydrocarbons and trace elements as indicators of contamination status near oil and gas platforms in the Sergipe-Alagoas Basin (Southwest Atlantic Ocean)

    NASA Astrophysics Data System (ADS)

    Lourenço, Rafael A.; Araujo Júnior, Marcus A. G.; Meireles Júnior, Ruy O.; Macena, Leandro F.; de A. Lima, Eleine Francioni; Carneiro, Maria Eulalia R.

    2013-12-01

    Oil and gas platforms from Sergipe-Alagoas Basin located in the northeastern region of Brazil do not discharge produced water. However, those platforms can be a potential source of contaminants to the marine environment due to their producing activities. In this study, sediment samples were collected in the vicinity of two offshore oil and gas platforms located in Sergipe-Alagoas Basin (PCM-9 and PGA-1) to evaluate the source and levels of hydrocarbons and trace elements (As, Fe, Al, Ti, Cu, Cd, Zn, Pb, Ni, Mn, Ba, V, Cr and Hg). Also, the potential impact of those platforms on the sediment quality was investigated. Polycyclic aromatic hydrocarbons diagnostic ratios observed in the sediment samples indicated hydrocarbons from pyrogenic source, specifically from biomass combustion. Trace elements As, Cd and Ba recorded concentrations higher than Threshold Effect Levels (TEL) in the sediment nearby the platforms. Also, there was evidence of some samples enriched by barium. Although As, Cd and Ba concentrations were higher than TEL, they most likely corresponded to background levels. The obtained results indicated that activities of the PCM-9 and PGA-1 platforms may not be affecting the quality of nearby sediment.

  2. Bioassay of polycyclic aromatic hydrocarbons

    SciTech Connect

    Van Kirk, E.A.

    1980-08-01

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

  3. Spatial distribution and composition of aliphatic hydrocarbons, polycyclic aromatic hydrocarbons and hopanes in superficial sediments of the coral reefs of the Persian Gulf, Iran.

    PubMed

    Ali, Ranjbar Jafarabadi; Alireza, Riyahi Bakhtiari; Mansour, Aliabadian; Amirhossein, Shadmehri Toosi

    2017-02-16

    This study is the first quantitative report on petroleum biomarkers from the coral reefs systems of the Persian Gulf. 120 reef surface sediment samples from ten fragile coral reef ecosystems were collected and analyzed for grain size, biogenic elements, elemental ratios, and petroleum biomarkers (n-alkanes, PAHs(1) and Hopanes) to assess the sources and early diagenesis of sedimentary organic matter. The mean grain size of the reef sediments ranged from 13.56 to 37.11% (Clay), 26.92 to 51.73% (Sand) and 35.97 to 43.85% (Silt). TOC(2) (3.35-9.72 mg.g(-1)) and TON(3) (0.4-1.10 mg.g(-1)) were identified as influencing factors on the accumulation of petroleum hydrocarbons, whilst BC(4) (1.08-3.28 mg.g(-1)) and TIN(5) (0.13-0.86) did not exhibit any determining effect. Although BC and TIN demonstrated heterogeneous spatial distribution, TOC and TON indicated homogenous distribution with continually upward trend in concentration from the east to west ward of the Gulf. The mean calculated TOC/TN ratios vacillated according to the stations (p < 0.05) from 2.96 at Shidvar Island to 8.64 at Hengam Island. The high TOC/TN ratios were observed in the Hengam (8.64), Kharg (8.04) and Siri (6.29), respectively, suggesting a predominant marine origin. The mean concentrations of ∑C11-35n-alkanes, ∑30 PAHs and ∑9Hopanes were found in the ranges of 385-937 μg.g(-1)dw, (overall mean:590 μg.g(-1)dw), 326-793 ng.g(-1)dw (499 ng.g(-1)dw), 88 to 568 μg.g(-1) d (258 ng.g(-1)dw), respectively. Higher concentrations of detected petroleum biomarkers in reef sediments were chiefly distributed near main industrial areas, Kharg, Lavan and Siri, whilst the lower concentrations were in Hormoz and Qeshm. In addition, one-way ANOVA(6) analysis demonstrated considerably significant differences (p < 0.05) among concentration of detected total petroleum hydrocarbons between most sampling locations. Some sampling sites especially Kharg, Lavan, Siri and Lark indicated higher

  4. Comparison of aliphatic hydrocarbons, polycyclic aromatic hydrocarbons, polychlorinated biphenyls, polybrominated diphenylethers, and organochlorine pesticides in Pacific sanddab (Citharichthys sordidus) from offshore oil platforms and natural reefs along the California coast

    USGS Publications Warehouse

    Gale, Robert W.; Tanner, Michael J.; Love, Milton S.; Nishimoto, Mary M.; Schroeder, Donna M.

    2013-01-01

    Recently, the relative exposure of Pacific sanddab (Citharichthys sordidus) to polycyclic aromatic hydrocarbons (PAHs) at oil-production platforms was reported, indicating negligible exposure to PAHs and no discernible differences between exposures at platforms and nearby natural areas sites. In this report, the potential for chronic PAH exposure in fish is reported, by measurement of recalcitrant, higher molecular weight PAHs in tissues of fish previously investigated for PAH metabolites in bile. A total of 34 PAHs (20 PAHs, 11 alkylated PAHs, and 3 polycyclic aromatic thiophenes) were targeted. In addition, legacy contaminants—polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs),—and current contaminants, polybrominated diphenylethers (PBDEs) linked to endocrine disruption, were measured by gas chromatography with electron-capture or mass spectrometric detection, to form a more complete picture of the contaminant-related status of fishes at oil production platforms in the Southern California Bight. No hydrocarbon profiles or unresolved complex hydrocarbon background were found in fish from platforms and from natural areas, and concentrations of aliphatics were low less than 100 nanograms per gram (ng/g) per component]. Total-PAH concentrations in fish ranged from 15 to 37 ng/g at natural areas and from 8.7 to 22 ng/g at platforms. Profiles of PAHs were similar at all natural and platform sites, consisting mainly of naphthalene and methylnaphthalenes, phenanthrene, fluoranthene, and pyrene. Total-PCB concentrations (excluding non-ortho-chloro-substituted congeners) in fish were low, ranging from 7 to 22 ng/g at natural areas and from 10 to 35 ng/g at platforms. About 50 percent of the total-PCBs at all sites consisted of 11 congeners: 153 > 138/163/164 > 110 > 118 > 15 > 99 > 187 > 149 > 180. Most OCPs, except dichlorodiphenyltrichloroethane (DDT)-related compounds, were not detectable or were at concentrations of less than 1 ng/g in fish. p

  5. Spreading coefficients of aliphatic hydrocarbons on water

    SciTech Connect

    Takii, Taichi; Mori, Y.H. . Dept. of Mechanical Engineering)

    1993-11-01

    Experiments have been performed to determine the equilibrium spreading coefficients of some aliphatic hydrocarbons (C[sub 6]C[sub 10]) on water. The thickness of a discrete lens of each hydrocarbon sample floating on a stagnant water pool was measured interferometrically and used to calculate the spreading coefficient of the hydrocarbon with the aid of Langmuir's capillarity theory. The dependences of the spreading coefficient, thus observed, on temperature (0--50 C) and on the number of carbon atoms in the hydrocarbon molecule are in qualitative agreement with the predictions based on the Lifshitz theory of van der Waals forces.

  6. Polycyclic Aromatic Hydrocarbons

    NASA Technical Reports Server (NTRS)

    Salama, Farid

    2010-01-01

    Carbonaceous materials play an important role in space. Polycyclic Aromatic Hydrocarbons (PAHs) are a ubiquitous component of the carbonaceous materials. PAHs are the best-known candidates to account for the IR emission bands. They are also thought to be among the carriers of the diffuse interstellar absorption bands (DIBs). PAH ionization states reflect the ionization balance of the medium while PAH size, composition, and structure reflect the energetic and chemical history of the medium. A major challenge is to reproduce in the laboratory the physical conditions that exist in the emission and absorption interstellar zones. The harsh physical conditions of the ISM -low temperature, collisionless, strong UV radiation fields- are simulated in the laboratory by associating a molecular beam with an ionizing discharge to generate a cold plasma expansion. PAH ions and radicals are formed from the neutral precursors in an isolated environment at low temperature and probed with high-sensitivity cavity ringdown spectroscopy in the NUV-NIR range. Carbon nanoparticles are also formed during the short residence time of the precursors in the plasma and are characterized with time-offlight mass spectrometry. These experiments provide unique information on the spectra of large carbonaceous molecules and ions in the gas phase that can now be directly compared to interstellar and circumstellar observations (IR emission bands, DIBs, extinction curve). These findings also hold great potential for understanding the formation process of interstellar carbonaceous grains. We will review recent progress in the experimental and theoretical studies of PAHs, compare the laboratory data with astronomical observations and discuss the global implications.

  7. THE PHOTOTOXICITY OF POLYCYCLIC AROMATIC HYDROCARBONS

    EPA Science Inventory

    The U.S. Environmental Protection Agency (EPA) continues to be interested in developing methods for the detection of polycyclic aromatic hydrocarbons (PAHS) in the environment. Polycyclic aromatic hydrocarbons (PAHS) are common contaminants in our environment. Being major product...

  8. Aliphatic hydrocarbons of the Murchison meteorite

    NASA Technical Reports Server (NTRS)

    Cronin, John R.; Pizzarello, Sandra

    1990-01-01

    Hydrocarbon fractions from the Murchison meteorite were prepared using benzene-methanol as the extraction solvent, fractionated on silica gel columns, and analyzed using gas chromatography combined with mass spectrometry and IR and NMR techniques. Results indicate that the most abundant aliphatic hydrocarbon components of the Murchison meteorite are C15 to C30 branched-alkyl-substituted mono-, di-, and tricyclic alkanes. It is shown that the n-alkanes, methyl alkanes, and isoprenoid alkanes that are sometimes found in extracts of the Murchison meteorite are terrestrial contaminants.

  9. Biofiltration of gasoline and diesel aliphatic hydrocarbons.

    PubMed

    Halecky, Martin; Rousova, Jana; Paca, Jan; Kozliak, Evguenii; Seames, Wayne; Jones, Kim

    2015-02-01

    The ability of a biofilm to switch between the mixtures of mostly aromatic and aliphatic hydrocarbons was investigated to assess biofiltration efficiency and potential substrate interactions. A switch from gasoline, which consisted of both aliphatic and aromatic hydrocarbons, to a mixture of volatile diesel n-alkanes resulted in a significant increase in biofiltration efficiency, despite the lack of readily biodegradable aromatic hydrocarbons in the diesel mixture. This improved biofilter performance was shown to be the result of the presence of larger size (C₉-C(12)) linear alkanes in diesel, which turned out to be more degradable than their shorter-chain (C₆-C₈) homologues in gasoline. The evidence obtained from both biofiltration-based and independent microbiological tests indicated that the rate was limited by biochemical reactions, with the inhibition of shorter chain alkane biodegradation by their larger size homologues as corroborated by a significant substrate specialization along the biofilter bed. These observations were explained by the lack of specific enzymes designed for the oxidation of short-chain alkanes as opposed to their longer carbon chain homologues.

  10. Polycyclic hydrocarbons and cancer

    SciTech Connect

    Gelboin, H.V.P; Ts'o, P.O.P.

    1981-01-01

    This book is Volume 3 of a three-volume series. It discusses polynuclear aromatic hydrocarbons (PAHs) in the marine environment, various PAH dihydrodiols, certain enzyme reactions, carcinogenesis modifications, and tumor promotion. PAH epidemiology for quantifying cigarette smoking and air pollution risks is also covered. (JMT)

  11. Aliphatic hydrocarbons and polycyclic aromatic hydrocarbons (PAHs) in sediments collected from the 110 mile hole and along a transect from 58 degrees 58.32'N 1 degree 10.38'W to the inner Moray Firth, Scotland.

    PubMed

    Webster, Lynda; Twigg, Marsailidh; Megginson, Colin; Walsham, Pam; Packer, Gill; Moffat, Colin

    2003-06-01

    Sediments were collected from the 110 mile hole and along a transect from 58 degrees 58.32' N 1 degree 10.38' W to the UK National Marine Monitoring (NMMP) site in the inner Moray Firth, for determination of hydrocarbon concentration and composition. Total PAH concentrations (2- to 6-ring PAHs, parent and branched) were highest at NMMP site 95 and at the associated end of the transect in the inner Moray Firth. PAHs in this area were of predominately pyrolytic origin and could be attributed to urban and industrial activities. The majority of sediments collected in the middle section of the transect had low total PAH concentrations (< 100 ng g(-1) dry weight). The high proportion of naphthalenes and alkylated PAHs in this area suggested a predominately petrogenic input. The GC-FID aliphatic hydrocarbon profiles showed that the majority of sediments, including those in the inner Firth, had a limited petrogenic input. This was supported by the geochemical biomarker profiles, which contained triterpanes typical of Middle Eastern crude oil. Principal component analysis was used to investigate spatial trends in the PAH distributions and demonstrated that there were differences between areas. The NMMP site 95 and transect start and middle sediments were well separated. PCA further confirmed that sediments from the NMMP site 95, the 110 mile hole and the inner Moray Firth (south west) end of the transect contained PAHs from predominately pyrolytic sources, whereas sediments from the north east end (start) and the middle of the transect were typified by a greater petrogenic component.

  12. Polycyclic aromatic hydrocarbons in carcinogenesis.

    PubMed Central

    Warshawsky, D

    1999-01-01

    A symposium on "Polycyclic Aromatic Hydrocarbons (PAHs) in Carcinogenesis" was presented at the third International Congress of Pathophysiology held in Lathi, Finland, 28 June-3 July 1998. The congress was also sponsored by the International Union of Biological Sciences and the International Society of Free Radical Research. Institutional support for the symposium included the Electric Power Research Institute, National Center for Toxicological Research, and EPA/National Health and Environmental Effects Research Laboratory and the Office of Solid Waste and Emergency Response. The symposium focused on the sources, carcinogenicity, genotoxicity, and risk assessment of individual and mixtures of PAHs that are found in solid wastes, Superfund sites, and other hazardous waste sites. Based on the occurrence of PAHs at numerous Superfund sites and the significant data gaps on the toxic potential of certain PAHs, the information developed during this symposium would be of value in assessing health risks of these chemicals at Superfund and other hazardous waste sites. PMID:10090712

  13. Biodegradation of polycyclic hydrocarbons by Phanerochaete chrysosporium

    EPA Science Inventory

    The ability of the white rot fungus Phanerochaete chrysosporium to degrade polycyclic aromatic hydrocarbons (PAHs) that are present in anthracene oil (a distillation product obtained from coal tar) was demonstrated. Analysis by capillary gas chromatography and high-performance li...

  14. Infrared Spectra of Polycyclic Aromatic Hydrocarbons (PAHs)

    NASA Technical Reports Server (NTRS)

    Bauschlicher, Charles W., Jr.; Bakes, E. L. O.

    2000-01-01

    We have computed the synthetic infrared spectra of some polycyclic aromatic hydrocarbons containing up to 54 carbon atoms. The species studied include ovalene, circumcoronene, dicoronylene, and hexabenzocoronene. We report spectra for anions, neutrals, cations, and multiply charged cations.

  15. Birds and polycyclic aromatic hydrocarbons

    USGS Publications Warehouse

    Albers, P.H.

    2006-01-01

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

  16. PROTONATED POLYCYCLIC AROMATIC HYDROCARBONS REVISITED

    SciTech Connect

    Ricca, Alessandra; Bauschlicher, Charles W. Jr; Allamandola, Louis J. E-mail: Charles.W.Bauschlicher@nasa.gov

    2011-02-01

    We reconsider the contribution that singly protonated polycyclic aromatic hydrocarbons (PAHs; HPAH{sup +}s) might make to the Class A component of the 6.2 {mu}m interstellar emission feature in light of the recent experimental measurements of protonated naphthalene and coronene. Our calculations on the small HPAH{sup +}s have a band near 6.2 {mu}m, as found in experiment. While the larger HPAH{sup +}s still have emission near 6.2 {mu}m, the much larger intensity of the band near 6.3 {mu}m overwhelms the weaker band at 6.2 {mu}m, so that the 6.2 {mu}m band is barely visible. Since the large PAHs are more representative of those in the interstellar medium, our work suggests that large HPAH{sup +}s cannot be major contributors to the observed emission at 6.2 {mu}m (i.e., Class A species). Saturating large PAH cations with hydrogen atoms retains the 6.2 {mu}m Class A band position, but the rest of the spectrum is inconsistent with observed spectra.

  17. Polycyclic Aromatic Hydrocarbons with SPICA

    NASA Astrophysics Data System (ADS)

    Berné, O.; Joblin, C.; Mulas, G.; Tielens, A. G. G. M.; Goicoechea, J. R.

    2009-12-01

    Thanks to high sensitivity, high angular resolution and broad spectral coverage, SPICA will offer a unique opportunity to better characterize the nature of polycyclic aromatic hydrocarbons (PAHs) and very small grains (VSGs), to better use them as probes of astrophysical environments. The angular resolution will enable to probe the chemical frontiers in the evolution process from VSGs to neutral PAHs, to ionized PAHs and to "Grand-PAHs" in photodissotiation regions and HII regions, as a function of G0 /n (UV radiation field / density). High sensitivity will favor the detection of the far-IR skeletal emission bands of PAHs, which provide specific fingerprints and could lead to the identification of individual PAHs. This overall characterization will allow to use PAH and VSG populations as tracers of physical conditions in spatially resolved protoplanetary disks and nearby galaxies (using mid-IR instruments), and in high redshift galaxies (using the far-IR instrument), thanks to the broad spectral coverage SPICA provides. Based on our previous experience with ISO and Spitzer we discuss how these goals can be reached.

  18. A Comprehensive Review of Aliphatic Hydrocarbon Biodegradation by Bacteria.

    PubMed

    Abbasian, Firouz; Lockington, Robin; Mallavarapu, Megharaj; Naidu, Ravi

    2015-06-01

    Hydrocarbons are relatively recalcitrant compounds and are classified as high-priority pollutants. However, these compounds are slowly degraded by a large variety of microorganisms. Bacteria are able to degrade aliphatic saturated and unsaturated hydrocarbons via both aerobic and anaerobic pathways. Branched hydrocarbons and cyclic hydrocarbons are also degraded by bacteria. The aerobic bacteria use different types of oxygenases, including monooxygenase, cytochrome-dependent oxygenase and dioxygenase, to insert one or two atoms of oxygen into their targets. Anaerobic bacteria, on the other hand, employ a variety of simple organic and inorganic molecules, including sulphate, nitrate, carbonate and metals, for hydrocarbon oxidation.

  19. Geochemistry of polycyclic aromatic hydrocarbons in Columbia River and Washington coastal sediments

    SciTech Connect

    Prahl, F.G.

    1982-01-20

    A field investigation was conducted to determine the origins, dispersal pathways and fates of polycyclic aromatic hydrocarbons (PAH) in a river-influenced coastal marine environment. Complete PAH characterizations were combined with analyses of aliphatic hydrocarbons, organic carbon and nitrogen, lignin, lead-210 and several other parameters to clarify the geochemistry of this class of compounds in the Columbia River basin and the southern Washington continental shelf and slope. 94 references, 18 figures, 24 tables.

  20. SPITZER'S VIEW ON AROMATIC AND ALIPHATIC HYDROCARBON EMISSION IN HERBIG Ae STARS

    SciTech Connect

    Acke, B.; Waters, L. B. F. M.; Bouwman, J.; Juhasz, A.; Henning, Th.; Van den Ancker, M. E.; Meeus, G.; Tielens, A. G. G. M.

    2010-07-20

    The chemistry of astronomical hydrocarbons, responsible for the well-known infrared emission features detected in a wide variety of targets, remains enigmatic. Here we focus on the group of young intermediate-mass Herbig Ae stars. We have analyzed the aliphatic and polycyclic aromatic hydrocarbon (PAH) emission features in the infrared spectra of a sample of 53 Herbig Ae stars, obtained with the Infrared Spectrograph aboard the Spitzer Space Telescope. We confirm that the PAH-to-stellar luminosity ratio is higher in targets with a flared dust disk. However, a few sources with a flattened dust disk still show relatively strong PAH emission. Since PAH molecules trace the gas disk, this indicates that gas disks may still be flared, while the dust disk has settled due to grain growth. There are indications that the strength of the 11.3 {mu}m feature also depends on dust disk structure, with flattened disks being less bright in this feature. We confirm that the CC bond features at 6.2 and 7.8 {mu}m shift to redder wavelengths with decreasing stellar effective temperature. Moreover, we show that this redshift is accompanied by a relative increase of aliphatic CH emission and a decrease of the aromatic 8.6 {mu}m CH feature strength. Cool stars in our sample are surrounded by hydrocarbons with a high aliphatic/aromatic CH ratio and a low aromatic CH/CC ratio, and vice versa for the hot stars. We conclude that, while the overall hydrocarbon emission strength depends on the dust disk's geometry, the relative differences seen in the IR emission features in disks around Herbig Ae stars are mainly due to chemical differences of the hydrocarbon molecules induced by the stellar UV field. Strong UV flux reduces the aliphatic component and emphasizes the spectral signature of the aromatic molecules in the IR spectra.

  1. Closed-Shell Polycyclic Aromatic Hydrocarbon Cations: A New Category of Interstellar Polycyclic Aromatic Hydrocarbons

    NASA Technical Reports Server (NTRS)

    Hudgins, Douglas M.; Bauschlicher, Charles W., Jr.; Allamandola, Louis J.; DeVincenzi, Donald (Technical Monitor)

    2001-01-01

    Density functional theory has been employed to calculate the harmonic frequencies and intensities of a range of polycyclic aromatic hydrocarbon (PAH) cations that explore both size and electronic structure effects of the infrared spectroscopic properties of these species. The sample extends the size range of PAH species considered to more than 50 carbon atoms and includes several representatives from each of two heretofore unexplored categories of PAH cations: (1) fully benzenoid PAH cations whose carbon skeleton is composed of an odd number of carbon atoms (C(sub odd) PAHs); and (2) protonated PAH cations (HPAH+). Unlike the radical electronic structures of the PAH cations that have been the subject of previous theoretical and experimental work, the species in these two classes have a closed-shell electronic configuration. The calculated spectra of circumcoronene, C54H18 in both neutral and (radical) cationic form are also reported and compared with those of the other species. Overall, the C(sub odd) PAHs spectra are dominated by strong CC stretching modes near 1600 cm(exp -1) and display spectra that are remarkably insensitive to molecular size. The HPAH+ species evince a more complex spectrum consistent with the added contributions of aliphatic modes and their generally lower symmetry. Finally, for both classes of closed-shell cations, the intensity of the aromatic CH stretching modes is found to increase with molecular size far out of proportion with the number of CH groups, approaching a value more typical of neutral PAHs for the largest species studied.

  2. Biodegradation of aliphatic vs. aromatic hydrocarbons in fertilized arctic soils

    USGS Publications Warehouse

    Braddock, J.F.

    1999-01-01

    A study was carried out to test a simple bioremediation treatment strategy in the Arctic and analyze the influence of fertilization the degradation of aliphatic and aromatic hydrocarbons, e.g., pristine, n-tetradecane, n-pentadecane, 2-methylnaphthalene, naphthalene, and acenaphthalene. The site was a coarse sand pad that once supported fuel storage tanks. Diesel-range organics concentrations were 250-860 mg/kg soil at the beginning of the study. Replicate field plots treated with fertilizer yielded final concentrations of 0, 50, 100, or 200 mg N/kg soil. Soil pH and soil-water potentials decreased due to fertilizer application. The addition of fertilizer considerably increased soil respiration potentials, but not the populations of microorganisms measured. Fertilizer addition also led to ??? 50% loss of measured aliphatic and aromatic hydrocarbons in surface and subsurface soils. For fertilized plots, hydrocarbon loss was not associated with the quantity of fertilizer added. Losses of aliphatic hydrocarbons were ascribed to biotic processes, while losses of aromatic hydrocarbons were due to biotic and abiotic processes.

  3. Dihydrodiol dehydrogenase and polycyclic aromatic hydrocarbon metabolism

    SciTech Connect

    Smithgall, T.E.

    1986-01-01

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

  4. Aerobic microorganism for the degradation of chlorinated aliphatic hydrocarbons

    DOEpatents

    Fliermans, Carl B.

    1989-01-01

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

  5. Monitoring of vapor phase polycyclic aromatic hydrocarbons

    DOEpatents

    Vo-Dinh, Tuan; Hajaligol, Mohammad R.

    2004-06-01

    An apparatus for monitoring vapor phase polycyclic aromatic hydrocarbons in a high-temperature environment has an excitation source producing electromagnetic radiation, an optical path having an optical probe optically communicating the electromagnetic radiation received at a proximal end to a distal end, a spectrometer or polychromator, a detector, and a positioner coupled to the first optical path. The positioner can slidably move the distal end of the optical probe to maintain the distal end position with respect to an area of a material undergoing combustion. The emitted wavelength can be directed to a detector in a single optical probe 180.degree. backscattered configuration, in a dual optical probe 180.degree. backscattered configuration or in a dual optical probe 90.degree. side scattered configuration. The apparatus can be used to monitor an emitted wavelength of energy from a polycyclic aromatic hydrocarbon as it fluoresces in a high temperature environment.

  6. Aliphatic hydrocarbons in Great Barrier Reef organisms and environment

    NASA Astrophysics Data System (ADS)

    Coates, M.; Connell, D. W.; Bodero, J.; Miller, G. J.; Back, R.

    1986-07-01

    This investigation was undertaken to assess the chemical nature, occurrence, and possible origin of petroleum hydrocarbons in the Great Barrier Reef ecosystem. Aliphatic hydrocarbons in surface sediments, water, and a suite of seven species from widely separated coral reefs in the Great Barrier Reef area were analysed by gas chromatography, and by gas chromatography coupled with mass spectrometry. The hydrocarbons found were substantially of biogenic origin. The major components were n-pentadecane, n-heptadecane, pristane and mono-alkenes based on heptadecane, and were believed to originate from benthic algae and phytoplankton. There was no evidence to suggest that lipid content had any influence on hydrocarbon content. Hydrocarbons from the organisms and sediments have characteristic composition patterns which would be altered by the presence of petroleum hydrocarbons. An unresolved complex mixture, usually considered indicative of petroleum contamination, was found in greater than trace amounts only in Holothuria (sea cucumber) and Acropora (coral) from the Capricorn Group, and in some sediment samples from the Capricorn Group and Lizard Island area.

  7. Bioremediation technologies for polycyclic aromatic hydrocarbon compounds

    SciTech Connect

    Alleman, B.C.; Leeson, A.

    1999-11-01

    Polycyclic aromatic hydrocarbon compounds (PAHs) are common and challenging contaminants that affect soil and sediments. Methods for treating PAHs have undergone change and refinement in the recent past, and this volume presents the latest trends in PAH remediation theory and practice. The papers in this volume cover topics ranging from the remediation of manufactured gas plant (MGP) sites to the remediation of sediments. The papers present lab and field studies, characterization studies, comparison studies, and descriptions of technologies ranging from composting to thermally enhanced bioremediation to fungal technologies and other innovative approaches.

  8. Characterization and analysis of polycyclic aromatic hydrocarbons

    SciTech Connect

    Breuer, G.M.; Smith, J.P.

    1984-01-01

    Sampling and analytical procedures were developed for determining the concentrations of polycyclic aromatic hydrocarbons in animal-exposure chambers during studies on exposure to diesel exhaust, coal dust, or mixtures of these two pollutants. Fluoranthene, pyrene, benzo(a)anthracene, chrysene, benzo(e)pyrene, benzo(k)fluoranthene, and benzo(a)pyrene were used as representative polycyclic aromatic hydrocarbons. High-pressure liquid chromatography with fluorescence detection was used for analysis. Coal-dust only samples revealed a broad, rising background in the chromatogram with small peaks superimposed corresponding to fluoranthene, pyrene, and benzo(a)anthracene, diesel exhaust only samples showed many peaks on a flat baseline including those corresponding to fluoranthene, pyrene, benzo(a)anthracene, benzo(k)fluoranthene, and benzo(a)pyrene. In general, no polynuclear aromatics were noted in the clean air samples. The authors note that relatively minor changes in air/fuel ratio, lubricant, fuel, and load may have substantial effects on very minor components of the exhaust emission.

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

    PubMed

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

    2015-01-01

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

  10. Polycyclic aromatic hydrocarbons and cancer in man

    SciTech Connect

    Mastrangelo, G.; Marzia, V.; Fadda, E.

    1996-11-01

    Various substances and industrial processes, surrogates of exposure to polycyclic aromatic hydrocarbons (PAHs), are currently classified as human carcinogens. This paper reviews recent epidemiological studies reporting direct evidence of the carcinogenic effects of PAHs in occupationally exposed subjects. Risks of lung and bladder cancer were dose dependent when PAHs were measured quantitatively and truly nonexposed groups were chosen for comparison. These new findings suggest that the current threshold limit value of 0.2 mg/m{sup 3} of benzene soluble matter (which indicates PAH exposure) is unacceptable because, after 40 years of exposure, it involves a relative risk of 1.2-1.4 for lung cancer and 2.2 for bladder cancer. 33 refs., 2 tabs.

  11. Microbe-aliphatic hydrocarbon interactions in soil: implications for biodegradation and bioremediation.

    PubMed

    Stroud, J L; Paton, G I; Semple, K T

    2007-05-01

    Aliphatic hydrocarbons make up a substantial portion of organic contamination in the terrestrial environment. However, most studies have focussed on the fate and behaviour of aromatic contaminants in soil. Despite structural differences between aromatic and aliphatic hydrocarbons, both classes of contaminants are subject to physicochemical processes, which can affect the degree of loss, sequestration and interaction with soil microflora. Given the nature of hydrocarbon contamination of soils and the importance of bioremediation strategies, understanding the fate and behaviour of aliphatic hydrocarbons is imperative, particularly microbe-contaminant interactions. Biodegradation by microbes is the key removal process of hydrocarbons in soils, which is controlled by hydrocarbon physicochemistry, environmental conditions, bioavailability and the presence of catabolically active microbes. Therefore, the aims of this review are (i) to consider the physicochemical properties of aliphatic hydrocarbons and highlight mechanisms controlling their fate and behaviour in soil; (ii) to discuss the bioavailability and bioaccessibility of aliphatic hydrocarbons in soil, with particular attention being paid to biodegradation, and (iii) to briefly consider bioremediation techniques that may be applied to remove aliphatic hydrocarbons from soil.

  12. ADSORPTION OF POLYCYCLIC AROMATIC HYDROCARBONS IN AGED HARBOR SEDIMENTS

    EPA Science Inventory

    Polycyclic aromatic hydrocarbons (PAHs) are a group of hydrophobic organic contaminants which have low aqueous solubilities and are common pollutants in harbor sediments. Adsorption and desorption isotherms for PAHs are conducted to study the abiotic sorption of PAHs in uncontami...

  13. PHOTOTOXICITY OF POLYCYCLIC AROMATIC HYDROCARBONS IN COASTAL GREAT LAKES WATERS

    EPA Science Inventory

    Photoinduced toxicity is the exacerbated toxicity of environmental contaminants by UV radiation. Photoinduced toxicity of polycyclic aromatic hydrocarbons (PAHs) has been well established in the laboratory for numerous aquatic species including larval fish. The contaminants sub-p...

  14. POLYCYCLIC AROMATIC HYDROCARBON (PAH) EXPOSURE OF 257 PRESCHOOL CHILDREN

    EPA Science Inventory

    We investigated the polycyclic aromatic hydrocarbon (PAH) exposure of 257 preschool children and their adult caregivers in their everyday environments. Participants were recruited randomly from eligible homes and daycare centers within six North Carolina (NC) and six Ohio (OH) c...

  15. Organochlorine compounds and aliphatic hydrocarbons in Pacific walrus blubber.

    PubMed

    Seagars, D J; Garlich-Miller, J

    2001-01-01

    Blubber samples were collected from 8 male and 19 female Pacific walrus (Odobenus rosmarus divergens) taken during a 1991 joint USA/USSR cruise traveling widely through the Bering Sea. Dieldrin was found at a level similar to that reported 10 years earlier; oxychlordane was found at a slightly higher concentration than reported previously (Taylor et aL, 1989). Heptachlor epoxide was detected for the first time and found at a low concentration. An initial testing for alpha-, beta- and gamma-HCH detected concentrations similar to those in other Bering Sea pinnipeds. Mean summation of PCB was 0.45 microg g(-1) wet weight in males and 0.16 microg g(-1) in females; only one sample was > 1 microg g(-1). Traces of aliphatic hydrocarbons were detected in all sampled animals, only pristane (x = 0.48 microg g(-1)) was found in concentrations > 1 microg g(-1). Small sample sizes, a lack of samples from immature animals, and uniformly low concentrations of contaminants precluded meaningful analysis of age-related effects and regional differences.

  16. Sources and distribution of aliphatic and polyaromatic hydrocarbons in sediments from the Neuquen River, Argentine Patagonia.

    PubMed

    Monza, Liliana B; Loewy, Ruth M; Savini, Mónica C; Pechen de d'Angelo, Ana M

    2013-01-01

    Spatial distribution and probable sources of aliphatic and polyaromatic hydrocarbons (AHs, PAHs) were investigated in surface sediments collected along the bank of the Neuquen River, Argentina. Total concentrations of aliphatic hydrocarbons ranged between 0.41 and 125 μg/g dw. Six stations presented low values of resolved aliphatic hydrocarbons and the n-alkane distribution indexes applied suggested a clear biogenic source. These values can be considered the baseline levels of aliphatic hydrocarbons for the river sediments. This constitutes important information for the assessment of future impacts since a strong impulse in the exploitation of shale gas and shale oil in these zones is nowadays undergoing. For the other 11 stations, a mixture of aliphatic hydrocarbons of petrogenic and biogenic origin was observed. The spatial distribution reflects local inputs of these pollutants with a significant increase in concentrations in the lower course, where two major cities are located. The highest values of total aliphatic hydrocarbons were found in this sector which, in turn, was the only one where individual PAHs were detected.

  17. A statistical approach to the interpretation of aliphatic hydrocarbon distributions in marine sediments

    USGS Publications Warehouse

    Rapp, J.B.

    1991-01-01

    Q-mode factor analysis was used to quantitate the distribution of the major aliphatic hydrocarbon (n-alkanes, pristane, phytane) systems in sediments from a variety of marine environments. The compositions of the pure end members of the systems were obtained from factor scores and the distribution of the systems within each sample was obtained from factor loadings. All the data, from the diverse environments sampled (estuarine (San Francisco Bay), fresh-water (San Francisco Peninsula), polar-marine (Antarctica) and geothermal-marine (Gorda Ridge) sediments), were reduced to three major systems: a terrestrial system (mostly high molecular weight aliphatics with odd-numbered-carbon predominance), a mature system (mostly low molecular weight aliphatics without predominance) and a system containing mostly high molecular weight aliphatics with even-numbered-carbon predominance. With this statistical approach, it is possible to assign the percentage contribution from various sources to the observed distribution of aliphatic hydrocarbons in each sediment sample. ?? 1991.

  18. Polycyclic aromatic hydrocarbon processing by cosmic rays

    NASA Astrophysics Data System (ADS)

    Micelotta, E. R.; Jones, A. P.; Tielens, A. G. G. M.

    2011-02-01

    Context. Cosmic rays are present in almost all phases of the ISM. Polycyclic aromatic hydrocarbons (PAHs) and cosmic rays represent an abundant and ubiquitous component of the interstellar medium. However, the interaction between them has never before been fully investigated. Aims: To study the effects of cosmic ray ion (H, He, CNO and Fe-Co-Ni) and electron bombardment of PAHs in galactic and extragalactic environments. Methods: We calculate the nuclear and electronic interactions for collisions between PAHs and cosmic ray ions and electrons with energies between 5 MeV/nucleon and 10 GeV, above the threshold for carbon atom loss, in normal galaxies, starburst galaxies and cooling flow galaxy clusters. Results: The timescale for PAH destruction by cosmic ray ions depends on the electronic excitation energy E0 and on the amount of energy available for dissociation. Small PAHs are destroyed faster, with He and the CNO group being the more effective projectiles. For electron collisions, the lifetime is independent of the PAH size and varies with the threshold energy T0. Conclusions: Cosmic rays process the PAHs in diffuse clouds, where the destruction due to interstellar shocks is less efficient. In the hot gas filling galactic halos, outflows of starburst galaxies and intra-cluster medium, PAH destruction is dominated by collisions with thermal ions and electrons, but this mechanism is ineffective if the molecules are in denser cloudlets and isolated from the hot gas. Cosmic rays can access the denser clouds and together with X-rays will set the lifetime of those protected PAHs. This limits the use of PAHs as a "dye" for tracing the presence of cold entrained material.

  19. Polycyclic aromatic hydrocarbon emissions from motorcycles

    NASA Astrophysics Data System (ADS)

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

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

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

    PubMed

    Miki, Shizuho; Uno, Seiichi; Ito, Kazuki; Koyama, Jiro; Tanaka, Hiroyuki

    2014-08-30

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

  1. 75 FR 8937 - Development of a Relative Potency Factor (RPF) Approach for Polycyclic Aromatic Hydrocarbon (PAH...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-02-26

    ... AGENCY Development of a Relative Potency Factor (RPF) Approach for Polycyclic Aromatic Hydrocarbon (PAH...) Approach for Polycyclic Aromatic Hydrocarbon (PAH) Mixtures'' (EPA/635/R-08/012A). The draft document was... of a Relative Potency Factor (RPF) Approach for Polycyclic Aromatic Hydrocarbon (PAH) Mixtures''...

  2. Fingerprinting aliphatic hydrocarbon pollutants over agricultural lands surrounding Tehran oil refinery.

    PubMed

    Bayat, Javad; Hashemi, Seyed Hossein; Khoshbakht, Korros; Deihimfard, Reza

    2016-11-01

    The analysis of aliphatic hydrocarbons, which are composed of n-alkanes as well as branched and cyclic alkanes, can be used to distinguish between the sources of hydrocarbon contamination. In this study, the concentration of aliphatic hydrocarbons, soil pH, and organic matter in agricultural soils located south of Tehran were monitored. Eighty-three soil samples were taken from two depth ranges of 0-30 and 30-60 cm. The results showed that aliphatic compounds ranged from 0.22-68.11 mg kg(-1) at the top to 0.33-53.18 mg kg(-1) at subsoil. The amount of hydrocarbons increases from the northern parts toward the south, and hydrocarbon pollutants originated from both petroleum and non-petroleum sources. Higher concentrations of aliphatic compounds in the southern parts indicated that, aside from the practice of irrigating with untreated wastewater, leakage from oil refinery storage tanks possibly contributed to soil pollution. The results also showed that several sources have polluted the agricultural soils. It is necessary to develop a new local pollution criterion as a diagnostic index that includes not only hydrocarbons but also other parameters such as heavy metal content in both soil and untreated wastewater, surface runoff, and other irrigation water resources to determine the exact origin of pollution.

  3. Seasonal distribution of aliphatic hydrocarbons in the Vaza Barris Estuarine System, Sergipe, Brazil.

    PubMed

    Barbosa, José Carlos S; Santos, Lukas G G V; Sant'Anna, Mércia V S; Souza, Michel R R; Damasceno, Flaviana C; Alexandre, Marcelo R

    2016-03-15

    The seasonal assessment of anthropogenic activities in the Vaza Barris estuarine river system, located in the Sergipe state, northeastern Brazil, was performed using the aliphatic hydrocarbon distribution. The aliphatic hydrocarbon and isoprenoid (Pristane and Phytane) concentrations ranged between 0.19 μg g(-1) and 8.5 μg g(-1) of dry weight. Data were analyzed using Kruskal-Wallis test, with significance level set at p<0.05, and no seasonality distribution change was observed. The Carbon Preference Index (CPI), associated with n-alkanes/n-C16, Low Molecular Weight/High Molecular Weight ratio (LMW/HMW) and Terrigenous to Aquatic Ratio (TAR) suggested biogenic input of aliphatic hydrocarbons for most samples, with significant contribution of higher plants.

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

    EPA Science Inventory

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

  5. METHODOLOGY OF AMBIENT AIR MONITORING FOR POLYCYCLIC AROMATIC HYDROCARBONS

    EPA Science Inventory

    In the last decade, several studies of polycyclic aromatic hydrocarbons (PAH) in ambient air in the U.S. specifically investigated (1) the sampling efficiency of two sorbents for PAH in air: XAD-2 and polyurethane foam (PUP); (2) the storage stability of PAH on quartz fiber fil...

  6. Biodegradation of aliphatic hydrocarbons in the presence of hydroxy cucurbit[6]uril.

    PubMed

    Pasumarthi, Rajesh; Kumar, Vikash; Chandrasekharan, Sivaraman; Ganguly, Anasuya; Banerjee, Mainak; Mutnuri, Srikanth

    2014-11-15

    Aliphatic hydrocarbons are one of the major environmental pollutants with reduced bioavailability. The present study focuses on the effect of hydroxy cucurbit[6]uril on the bioavailability of hydrocarbons. A bacterial consortium was used for biodegradation studies under saline and non-saline conditions. Based on denaturing gradient gel electrophoresis results it was found that the consortium under saline conditions had two different strains. The experiment was conducted in microcosms with tetradecane, hexadecane, octadecane and mixture of the mentioned hydrocarbons as the sole carbon source. The residual hydrocarbon was quantified using gas chromatography every 24h. It was found that biodegradation of tetradecane and hexadecane, as individual carbon source increased in the presence of hydroxy CB[6], probably due to the increase in their bioavailability. In case of octadecane this did not happen. Bioavailability of all three aliphatic hydrocarbons was increased when provided as a mixture to the consortium under saline conditions.

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

    NASA Technical Reports Server (NTRS)

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

    2002-01-01

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

  8. SELECTIVE ENUMERATION OF AROMATIC AND ALIPHATIC HYDROCARBON DEGRADING BACTERIA BY A MOST-PROBABLE-NUMBER PROCEDURE

    EPA Science Inventory

    A most-portable-number (MPN) procedure was developed to separately enumerate aliphatic and aromatic hydrocarbon degrading bacteria, because most of the currently available methods are unable to distinguish between these two groups. Separate 96-well microtiter plates are used to ...

  9. Hybrid membranes of metal-organic molecule nanocages for aromatic/aliphatic hydrocarbon separation by pervaporation.

    PubMed

    Zhao, Cui; Wang, Naixin; Wang, Lin; Huang, Hongliang; Zhang, Rong; Yang, Fan; Xie, Yabo; Ji, Shulan; Li, Jian-Rong

    2014-11-21

    Hybrid membranes composed of porous metal-organic molecule nanocages as fillers embedded in a hyperbranched polymer (Boltorn W3000) were fabricated, which exhibit excellent pervaporation separation performances towards aromatic/aliphatic hydrocarbons. The unique nature of the molecule-based fillers and their good dispersion and compatibility in/with the polymer are responsible for the good membrane properties.

  10. Preliminary chemical analysis and biological testing of materials from the HRI catalytic two-stage liquefaction (CTSL) process. [Aliphatic hydrocarbons

    SciTech Connect

    Later, D.W.; Wilson, B.W.

    1985-01-01

    Coal-derived materials from experimental runs of Hydrocarbon Research Incorporated's (HRI) catalytic two-stage liquefaction (CTSL) process were chemically characterized and screened for microbial mutagenicity. This process differs from two-stage coal liquefaction processes in that catalyst is used in both stages. Samples from both the first and second stages were class-fractionated by alumina adsorption chromatography. The fractions were analyzed by capillary column gas chromatography; gas chromatography/mass spectrometry; direct probe, low voltage mass spectrometry; and proton nuclear magnetic resonance spectrometry. Mutagenicity assays were performed with the crude and class fractions in Salmonella typhimurium, TA98. Preliminary results of chemical analyses indicate that >80% CTSL materials from both process stages were aliphatic hydrocarbon and polynuclear aromatic hydrocarbon (PAH) compounds. Furthermore, the gross and specific chemical composition of process materials from the first stage were very similar to those of the second stage. In general, the unfractionated materials were only slightly active in the TA98 mutagenicity assay. Like other coal liquefaction materials investigated in this laboratory, the nitrogen-containing polycyclic aromatic compound (N-PAC) class fractions were responsible for the bulk of the mutagenic activity of the crudes. Finally, it was shown that this activity correlated with the presence of amino-PAH. 20 figures, 9 tables.

  11. Determination of polycyclic aromatic hydrocarbons in diesel exhaust particulate matter and diesel fuel oil.

    PubMed

    Obuchi, A; Aoyama, H; Ohi, A; Ohuchi, H

    1984-11-16

    Clean-up procedures were developed for a method for determining the amount of polycyclic aromatic hydrocarbons (PAHs) in diesel exhaust particulate matter and in diesel fuel oils using reversed-phase high-performance liquid chromatography (HPLC). They were based mainly on the elimination of insoluble matter and aliphatic compounds that affect the performance of HPLC, from the dichloromethane extracts of particulate matter or from oils, with the aid of a disposable preparation column containing reversed-phase packings (Sep-Pak C18). Using these procedures, it is possible to detect 1 ng of benzo(a)pyrene in 30 mg of particulate matter with more than a 97% recovery or 0.5 ng in 50 microliters of oil with 91% recovery. Examples of analyses are given for particulate matter emitted from a diesel test engine and for diesel fuel oils, such as gas oil, residual oil and coal-liquefied oil.

  12. Cyclophanes containing large polycyclic aromatic hydrocarbons.

    PubMed

    Ghasemabadi, Parisa Ghods; Yao, Tieguang; Bodwell, Graham J

    2015-09-21

    Cyclophanes have been firmly entrenched as a distinct class of compounds for well over half a century. The two main factors that have kept this field of chemistry going so strongly for such a long time are tremendous structural diversity and the interesting behaviour that is often observed. Although a very large number cyclophanes has been reported, only a very small proportion of them contain polycyclic aromatic systems that can be thought of as "large", i.e. with ≥4 rings. This Review puts the spotlight on such cyclophanes, illuminating both the chemistry that was used to synthesize them and what was learned from studying them. Context for the main body is provided by the careful consideration of the anatomy of a cyclophane and the classification of general synthetic approaches. The subsequent sections cover eleven different PAHs and are organized primarily according to increasing size of the aromatic system, starting with pyrene (C16, the only large polycyclic aromatic system to have been incorporated into numerous cyclophanes) and ending with hexabenzo[bc,ef,hi,kl,no,qr]coronene (C42).

  13. Direct photolysis of polycyclic aromatic hydrocarbons in drinking water sources.

    PubMed

    Sanches, S; Leitão, C; Penetra, A; Cardoso, V V; Ferreira, E; Benoliel, M J; Crespo, M T Barreto; Pereira, V J

    2011-09-15

    The widely used low pressure lamps were tested in terms of their efficiency to degrade polycyclic aromatic hydrocarbons listed as priority pollutants by the European Water Framework Directive and the U.S. Environmental Protection Agency, in water matrices with very different compositions (laboratory grade water, groundwater, and surface water). Using a UV fluence of 1500 mJ/cm(2), anthracene and benzo(a)pyrene were efficiently degraded, with much higher percent removals obtained when present in groundwater (83-93%) compared to surface water (36-48%). The removal percentages obtained for fluoranthene were lower and ranged from 13 to 54% in the different water matrices tested. Several parameters that influence the direct photolysis of polycyclic aromatic hydrocarbons were determined and their photolysis by-products were identified by mass spectrometry. The formation of photolysis by-products was found to be highly dependent on the source waters tested.

  14. Phylogenetic comparison of two polycyclic aromatic hydrocarbon-degrading mycobacteria.

    PubMed Central

    Govindaswami, M; Feldhake, D J; Kinkle, B K; Mindell, D P; Loper, J C

    1995-01-01

    Two mycobacterial strains previously isolated from fossil-fuel-contaminated environments and shown to degrade four- and/or five-ring polycyclic aromatic hydrocarbons were further characterized. The two strains, PYR-I and RJGII-135, had similar growth characteristics, colony morphologies, and scotochromogenic pigmentations. DNA amplification fingerprints obtained with total genomic DNA indicated some strain similarities but with several distinctly different bands. Moreover, phylogenetic analysis based upon essentially full-length 16S rRNA gene sequences separates the two strains as distinct species within the fast-growing group of mycobacteria. Although both strains are thermosensitive, strain PYR-I has the bulged U between positions 184 and 193 characteristic of thermotolerant mycobacteria. Both strains are of potential use for reintroduction into and bioremediation of polycyclic aromatic hydrocarbon-contaminated soils. PMID:7574631

  15. Oxidation of polycyclic aromatic hydrocarbons under sulfate-reducing conditions

    USGS Publications Warehouse

    Coates, J.D.; Anderson, R.T.; Lovley, D.R.

    1996-01-01

    [14C]naphthalene and phenanthrene were oxidized to 14CO2 without a detectable lag under strict anaerobic conditions in sediments from San Diego Bay, San Diego, Calif., that were heavily contaminated with polycyclic aromatic hydrocarbons (PAHs) but not in less contaminated sediments. Sulfate reduction was necessary for PAH oxidation. These results suggest that the self-purification capacity of PAH-contaminated sulfate-reducing environments may be greater than previously recognized.

  16. THE INFRARED SPECTROSCOPY OF NEUTRAL POLYCYCLIC AROMATIC HYDROCARBON CLUSTERS

    SciTech Connect

    Ricca, Alessandra; Bauschlicher, Charles W. Jr.; Allamandola, Louis J. E-mail: Charles.W.Bauschlicher@nasa.gov

    2013-10-10

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

  17. Critically Evaluated Thermochemical Properties of Polycyclic Aromatic Hydrocarbons

    NASA Astrophysics Data System (ADS)

    Roux, María Victoria; Temprado, Manuel; Chickos, James S.; Nagano, Yatsuhisa

    2008-12-01

    Experimental thermochemical properties of benzene, toluene, and 63 polycyclic aromatic hydrocarbons, published within the period 1878-2008 (over 350 references), are reported. Available experimental data for the enthalpies of combustion used to calculate enthalpies of formation in the condensed state, combined with sublimation, vaporization, and fusion enthalpies, are critically evaluated. Whenever possible, recommended values for these thermochemical properties and for the enthalpies of formation in the gas state at T =298.15K are provided.

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

    SciTech Connect

    Mulas, Giacomo; Casu, Silvia; Cecchi-Pestellini, Cesare; Zonca, Alberto E-mail: silvia@oa-cagliari.inaf.it E-mail: azonca@oa-cagliari.inaf.it

    2013-07-01

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

  19. Composition, distribution, and characterization of polycyclic aromatic hydrocarbons in soil in Linfen, China

    SciTech Connect

    Fu, S.; Cheng, H.X.; Liu, Y.H.; Xia, X.J.; Xu, X.B.

    2009-02-15

    A total of 10 surface soil samples representing the entire area of Linfen City were collected and analyzed for the presence of 16 polycyclic aromatic hydrocarbons. The total polycyclic aromatic hydrocarbon concentration ranged from 1.1 to 63.7 {mu} g g{sup -1}. Analysis of the sources of contamination revealed that polycyclic aromatic hydrocarbons in the soil were derived from combustion sources. Specifically, the primary source of polycyclic aromatic hydrocarbons was coal combustion, but the samples were also effected to varying degrees by traffic emissions. Furthermore, increased levels of contamination were observed in northeast Linfen due to the distribution of industrial plants.

  20. Molecular Tracers of Saturated and Polycyclic Aromatic Hydrocarbon Inputs into Central Park Lake, New York City

    PubMed Central

    YAN, BEIZHAN; ABRAJANO, TEOFILO A.; BOPP, RICHARD F.; CHAKY, DAMON A.; BENEDICT, LUCILLE A.; CHILLRUD, STEVEN N.

    2011-01-01

    Saturated hydrocarbons (SH) and polycyclic aromatic hydrocarbons (PAHs) have been quantified in a sediment core obtained from Central Park Lake, New York City. Radionuclides 210Pb and 137Cs were used to assign approximate dates to each individual section in the core. The dating profile based on 210Pb matches very well with the time constraints provided by 137Cs. Radionuclide-derived depositional dates are consistent with temporal information from the petroleum-indicator ratio U/R [the ratio of unresolved complex mixture (UCM) to saturated hydrocarbons in the aliphatic fraction] and the history of fuel use in the NYC area. Ratios of 1,7-dimethylphenanthrane (DMP) to 1,7-DMP plus 2,6-DMP [1,7/(1,7 + 2,6)-DMP], retene to retene plus chrysene [Ret/(Ret + Chy)], and fluoranthene to fluoranthene plus pyrene [Fl/(Fl + Py)] provide additional source discrimination throughout the core. Results show that the ratio U/R is sensitive to petroleum inputs and Ret/(Ret + Chy) is responsive to contributions from softwood combustion, whereas both Fl/(Fl + Py) and 1,7/(1,7 + 2,6)-DMP can be used to discriminate among wood, coal, and petroleum combustion sources. Combined use of these ratios suggests that in New York City, wood combustion dominated 100 years ago, with a shift to coal combustion occurring from the 1900s to the 1950s. Petroleum use began around the 1920s and has dominated since the 1940s. PMID:16201624

  1. The distribution and sources of polycyclic aromatic hydrocarbons in surface sediments along the Egyptian Mediterranean coast.

    PubMed

    El Nemr, Ahmed; Said, Tarek O; Khaled, Azza; El-Sikaily, Amany; Abd-Allah, Aly M A

    2007-01-01

    Coastal marine sediment samples were collected from 31 sampling stations along the Egyptian Mediterranean Sea coast. All sediment samples were analyzed to determine aliphatic and polycyclic aromatic hydrocarbons (PAHs) as well as total organic carbon (TOC) contents and grain size analysis. Total concentrations of 16 EPA-PAHs in the sediments were varied from 88 to 6338 ng g(-1) with an average value of 154 ng g(-1) (dry weight). However, the concentrations of total aliphatic were varied from 1.3 to 69.9 ng g(-1) with an average value of 15.6 ng g(-1) (dry weight). The highest contents of PAHs were found in the Eastern harbor (6338 ng g(-1)), Manzala (5206 ng g(-1)) and El-Jamil East (4895 ng g(-1)) locations. Good correlations observed between a certain numbers of PAH concentrations allowed to identify its origin. The average total organic carbon (TOC) percent was varied from 0.91 to 4.54%. Higher concentration of total pyrolytic hydrocarbons ( summation operatorCOMB) than total fossil hydrocarbons ( summation operatorPHE) declared that atmospheric fall-out is the significant source of PAHs to marine sediments of the Egyptian Mediterranean coast. The selected marked compounds, a principal component analysis (PCA) and special PAHs compound ratios (phenanthrene/anthracene vs fluoranthene/pyrene; summation operatorCOMB/ summation operatorEPA-PAHs) suggest the pyrogenic origins, especially traffic exhausts, are the dominant sources of PAHs in most locations. Interferences of rather petrogenic and pyrolytic PAH contaminations were noticed in the harbors due to petroleum products deliveries and fuel combustion emissions from the ships staying alongside the quays.

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

    PubMed Central

    Chang, H L; Alvarez-Cohen, L

    1996-01-01

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

  3. Atmospheric chlorinated polycyclic aromatic hydrocarbons in East Asia.

    PubMed

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

    2014-09-01

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

  4. Temperature dependence of infrared bands produced by polycyclic aromatic hydrocarbons

    NASA Astrophysics Data System (ADS)

    Colangeli, L.; Mennella, V.; Bussoletti, E.

    1992-02-01

    The behavior of IR absorption bands with temperature has been examined systematically in the laboratory for three representative polycyclic aromatic hydrocarbon molecules: coronene, chrysene, and 1-methylcoronene. A careful description of both intensity and profile measured for most of the bands is reported. A tentative interpretation of the observed variations is given in terms of extra-molecular effects produced by the anharmonicity of the vibrational energy levels as a function of temperature. These new laboratory data provide an accurate description of the optical properties for representative molecules often used to account for the so-called unidentified infrared bands emitted by astronomical sources.

  5. Polycyclic aromatic hydrocarbons, tobacco smoke, and epigenetic remodeling in asthma

    PubMed Central

    Klingbeil, E. C.; Hew, K. M.; Nygaard, U. C.; Nadeau, K. C.

    2014-01-01

    Environmental determinants including aerosolized pollutants such as polycyclic aromatic hydrocarbons (PAHs) and tobacco smoke have been associated with exacerbation and increased incidence of asthma. The influence of aerosolized pollutants on the development of immune dysfunction in asthmatics has been suggested to be mediated through epigenetic remodeling. Genome accessibility and transcription are regulated primarily through DNA methylation, histone modification, and microRNA transcript silencing. Epigenetic remodeling has been shown in studies to be associated with Th2 polarization and associated cytokine and chemokine regulation in the development of asthma. This review will present evidence for the contribution of the aerosolized pollutants PAH and environmental tobacco smoke to epigenetic remodeling in asthma. PMID:24760221

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

    SciTech Connect

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

    2009-02-15

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

  7. Dimerization of polycyclic aromatic hydrocarbons in soot nucleation.

    PubMed

    Zhang, Hong-Bo; You, Xiaoqing; Wang, Hongmiao; Law, Chung K

    2014-02-27

    A possible pathway of soot nucleation, in which localized π electrons play an important role in binding the polycyclic aromatic hydrocarbon (PAH) molecules having multiradical characteristics to form stable polymer molecules through covalent bonds, is studied using density functional and semiempirical methods. Results show that the number of covalent bonds formed in the dimerization of two identical PAHs is determined by the radical character, and the sites to form bonds are related to the aromaticity of individual six-membered ring structure. It is further shown that the binding energy of dimerization increases linearly with the diradical character in the range relevant to soot nucleation.

  8. Extraction Techniques for Polycyclic Aromatic Hydrocarbons in Soils

    PubMed Central

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

    2010-01-01

    This paper aims to provide a review of the analytical extraction techniques for polycyclic aromatic hydrocarbons (PAHs) in soils. The extraction technologies described here include Soxhlet extraction, ultrasonic and mechanical agitation, accelerated solvent extraction, supercritical and subcritical fluid extraction, microwave-assisted extraction, solid phase extraction and microextraction, thermal desorption and flash pyrolysis, as well as fluidised-bed extraction. The influencing factors in the extraction of PAHs from soil such as temperature, type of solvent, soil moisture, and other soil characteristics are also discussed. The paper concludes with a review of the models used to describe the kinetics of PAH desorption from soils during solvent extraction. PMID:20396670

  9. Importance of fundamental sp, sp2, and sp3 hydrocarbon radicals in the growth of polycyclic aromatic hydrocarbons.

    PubMed

    Shukla, Bikau; Koshi, Mitsuo

    2012-06-05

    The most basic chemistry of products formation in hydrocarbons pyrolysis has been explored via a comparative experimental study on the roles of fundamental sp, sp(2), and sp(3) hydrocarbon radicals/intermediates such as ethyne/ethynyl (C(2)H(2)/C(2)H), ethene/ethenyl (C(2)H(4)/C(2)H(3)), and methane/methyl (CH(4)/CH(3)) in products formations. By using an in situ time-of-flight mass spectrometry technique, gas-phase products of pyrolysis of acetylene (ethyne, C(2)H(2)), ethylene (ethene, C(2)H(4)), and acetone (propanone, CH(3)COCH(3)) were detected and found to include small aliphatic products to large polycyclic aromatic hydrocarbons (PAHs) of mass 324 amu. Observed products mass spectra showed a remarkable sequence of mass peaks at regular mass number intervals of 24, 26, or 14 indicating the role of the particular corresponding radicals, ethynyl (C(2)H), ethenyl (C(2)H(3)), or methyl (CH(3)), in products formation. The analysis of results revealed the following: (a) product formation in hydrocarbon pyrolysis is dominated by hydrogen abstraction and a vinyl (ethenyl, C(2)H(3)) radical addition (HAVA) mechanism, (b) contrary to the existing concept of termination of products mass growth at cyclopenta fused species like acenaphthylene, novel pathways forming large PAHs were found succeeding beyond such cyclopenta fused species by the further addition of C(2)H(x) or CH(3) radicals, (c) production of cyclopenta ring-fused PAHs (CP-PAHs) such as fluoranthene/corannulene appeared as a preferred route over benzenoid species like pyrene/coronene, (d) because of the high reactivity of the CH(3) radical, it readily converts unbranched products into products with aliphatic chains (branched product), and (e) some interesting novel products such as dicarbon monoxide (C(2)O), tricarbon monoxide (C(3)O), and cyclic ketones were detected especially in acetone pyrolysis. These results finally suggest that existing kinetic models of product formation should be modified to include

  10. Synthesis of condensed phases containing polycyclic aromatic hydrocarbons fullerenes and nanotubes

    DOEpatents

    Reilly, Peter T. A.

    2004-10-19

    The invention relates to methods for producing polycyclic aromatic hydrocarbons, fullerenes, and nanotubes, comprising: a. heating at least one carbon-containing material to form a condensed phase comprising at least one polycyclic aromatic hydrocarbon; b. collecting at least some of the condensed phase; c. reacting the condensed phase to form fullerenes and/or nanotubes.

  11. Polycyclic aromatic hydrocarbons in dust emitted from stoker - fired boilers.

    PubMed

    Kozielska, B; Konieczynski, J

    2007-08-01

    In the present paper, results of investigations of Polycyclic Aromatic Hydrocarbons (PAHs) in granulometric fractions of dust, emitted from 9 hard coal fired mechanic stoker boilers, are presented. Exhaust gases were sampled with a Mark III dust sampler. Extracts derived from the dust fractions were analysed by using Gas Chromatography (GC). The 16 PAHs, total PAHs and equivalent benzo(a)pyrene (B(a)P) were determined. Results of measurements averaged over all examined boilers are presented as concentrations, contents and contributions of investigated hydrocarbons to particular standardised fractions of dust classified according to particle sizes. Distributions of PAHs and their profiles in the dust fractions were determined. The emission factors for B(a)P and Toxic Equivalent B(a)P (TE B(a)P) were determined and proved to be several times higher than for pulverised fuel fired boilers. In the emitted dust, 73% of the total PAHs most hazardous to human health are comprised in PM1.

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

    NASA Technical Reports Server (NTRS)

    Deamer, D. W.

    1992-01-01

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

  13. IUPAC-NIST Solubility Data Series. 101. Alcohols + Hydrocarbons + Water. Part 2. C1-C3 Alcohols + Aliphatic Hydrocarbons

    NASA Astrophysics Data System (ADS)

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

    2016-09-01

    The mutual solubilities and related liquid-liquid equilibria for 37 ternary systems of C1-C3 alcohols with aliphatic hydrocarbons and water are exhaustively and critically reviewed. Reports of experimental determination of solubility that appeared in the primary literature prior to the end of 2012 are compiled. For 14 systems, sufficient data are available (two or more independent determinations) to allow critical evaluation. All data are expressed as mass percent and mole fraction as well as the originally reported units. In addition to the standard evaluation criteria used throughout the Solubility Data Series, an additional criterion was used for each of the evaluated systems. These systems include one binary miscibility gap in the hydrocarbon + water subsystem and another one can be in the methanol + hydrocarbon subsystem. The binary tie lines were compared with the recommended values published previously.

  14. Assessment of polycyclic aromatic hydrocarbons (PAHs) pollution in soil of suburban areas in Tianjin, China.

    PubMed

    Lv, Jungang; Shi, Rongguang; Cai, Yanming; Liu, Yong

    2010-07-01

    Soil contamination with polycyclic aromatic hydrocarbons is an increasing problem and has aroused more and more concern in many countries, including China. In this study, representative soil samples (n = 87) of suburban areas in Tianjin (Xiqing, Dongli, Jinnan, Beichen) were evaluated for 16 polycyclic aromatic hydrocarbons. Surface soil samples were air-dried and sieved. Microwave assisted extraction was used for polycyclic aromatic hydrocarbons preparation prior to analysis with gas chromatography-mass spectrometry. The total concentrations of tested polycyclic aromatic hydrocarbons in Xiqing, Dongli, Jinnan, Beichen ranged in 58.5-2,748.3, 36.1-6,734.7, 58.5-4,502.5, 29.7-852.5 ng/g and the averages of total concentration of polycyclic aromatic hydrocarbons were 600.5, 933.6, 640.8, 257.3 ng/g, respectively. Spatial variation of polycyclic aromatic hydrocarbons in soil was illustrated; Pollution status and comparison to other cities were also investigated. Serious polycyclic aromatic hydrocarbons soil pollution was found in Dongli district, on the contrary, Bap in most sites in Beichen did not exceed relative standards and most sites in Beichen should be classified as non-contaminated soil. Principal component analysis was used to identify the possible sources of different districts. It turned out that coal combustion still was the most important sources in three districts except Beichen. Coking, traffic, cooking, biomass combustion also accounted for polycyclic aromatic hydrocarbons pollution to certain extent in different districts. These data can be further used to assess the health risk associated with soils polluted with polycyclic aromatic hydrocarbons and help local government find proper way to reduce polycyclic aromatic hydrocarbons pollution in soils.

  15. Consensus sediment quality guidelines for polycyclic aromatic hydrocarbon mixtures

    SciTech Connect

    Swartz, R.C.

    1999-04-01

    Sediment quality guidelines (SQGs) for polycyclic aromatic hydrocarbons (PAHs) have been derived from a variety of laboratory, field, and theoretical foundations. They include the screening level concentration, effects ranges-low and -median, equilibrium partitioning concentrations, apparent effects threshold, {Sigma}PAH model, and threshold and probable effects levels. The resolution of controversial differences among the PAH SQGs lies in an understanding of the effects of mixtures. Polycyclic aromatic hydrocarbons virtually always occur in field-collected sediment as a complex mixture of covarying compounds. When expressed as a mixture concentration, that is, total PAH (TPAH), the guidelines form three clusters that were intended in their original derivations to represent threshold (TEC = 290 {micro}g/g organic carbon [OC]), median (MEC = 1,800 {micro}g/g OC), and extreme (EEC = 10,000 {micro}g/g OC) effects concentrations. The TEC/MEC/EEC consensus guidelines provide a unifying synthesis of other SQGs, reflect causal rather than correlative effects, account for mixtures, and predict sediment toxicity and benthic community perturbations at sites of PAH contamination. The TEC offers the most useful SQG because PAH mixtures are unlikely to cause adverse effects on benthic ecosystems below the TEC.

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

    PubMed

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

    2016-05-15

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

  17. Mild Aliphatic and Benzylic Hydrocarbon C-H Bond Chlorination Using Trichloroisocyanuric Acid.

    PubMed

    Combe, Sascha H; Hosseini, Abolfazl; Parra, Alejandro; Schreiner, Peter R

    2017-03-03

    We present the controlled monochlorination of aliphatic and benzylic hydrocarbons with only 1 equiv of substrate at 25-30 °C using N-hydroxyphthalimide (NHPI) as radical initiator and commercially available trichloroisocyanuric acid (TCCA) as the chlorine source. Catalytic amounts of CBr4 reduced the reaction times considerably due to the formation of chain-carrying ·CBr3 radicals. Benzylic C-H chlorination affords moderate to good yields for arenes carrying electron-withdrawing (50-85%) or weakly electron-donating groups (31-73%); cyclic aliphatic substrates provide low yields (24-38%). The products could be synthesized on a gram scale followed by simple purification via distillation. We report the first direct side-chain chlorination of 3-methylbenzoate affording methyl 3-(chloromethyl)benzoate, which is an important building block for the synthesis of vasodilator taprostene.

  18. Polycyclic aromatic hydrocarbons in sediments of China Sea.

    PubMed

    Li, Yanxia; Duan, Xiaoyong

    2015-10-01

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

  19. Polycyclic Aromatic Hydrocarbons and Infrared Astrophysics with Spitzer

    NASA Technical Reports Server (NTRS)

    Hudgins, Douglas M.; Allamandola, L. J.

    2004-01-01

    Over the past fifteen years, thanks to significant, parallel advancements in observational, experimental, and theoretical techniques, tremendous strides have been made in our understanding of the role that carbon-rich plays in the interstellar medium (ISM). Twenty years ago, the possible existence of an abundant population of large, carbon-rich molecules in the ISM was unthinkable. Today, the unmistakable spectroscopic signatures of polycyclic aromatic hydrocarbons (PAHs) - shockingly large molecules by the standards of traditional interstellar chemistry -are recognized throughout the Universe. In this presentation, we will examine the current state of the interstellar PAH model and explore how this data, in conjunction with the unparalleled observational data provided by the Spitzer Space Telescope, can be used to draw ever-deeper insights into the physical and chemical natures of a wide range of astrophysical environments.

  20. Polycyclic Aromatic Hydrocarbons in Mussels from a South American Estuary.

    PubMed

    Oliva, Ana L; Arias, Andrés H; Quintas, Pamela Y; Buzzi, Natalia S; Marcovecchio, Jorge E

    2017-03-18

    Bivalves, especially mussels, have been pointed as putative species to monitor polycyclic aromatic hydrocarbons (PAHs) in marine environment. After several environmental PAHs baseline reports, the present study was conducted to assess for the first time the levels of PAHs in native mussels (Brachidontes rodriguezii) collected from a critical industrialized estuary of Argentina. Under this objective, after an 18-month sampling period, 34 pools of mussels were assessed for 17 PAHs, including the 16 compounds prioritized by United States Environmental Protection Agency. By means of gas chromatography-mass spectrometry analysis, results showed total PAHs concentrations in mussel's tissue ranged from under laboratory detection limits to 482.4 ng/g dry weight. Mussel body burdens were dominated by lower molecular weight PAHs, such as phenanthrene, naphthalene, and pyrene, whereas the overall PAHs profile suggested the predominance of petrogenic sources. Finally, the potential ecotoxicological impact was evaluated by applying Environmental Assessment Criteria and benzo[a]pyrene toxic equivalent factors.

  1. Polycyclic aromatic hydrocarbon removal from water by natural fiber sorption.

    PubMed

    Khan, Eakalak; Khaodhir, Sutha; Rotwiron, Paritta

    2007-08-01

    The use of two natural sorbents, kapok and cattail fibers, were investigated for polycyclic aromatic hydrocarbon (PAH) removal from water. Naphthalene, acenaphthylene, acenaphthene, fluorene, phenanthrene, anthracene, and fluoranthene were the PAHs studied. For comparative purposes, a commercial polyester fiber sorbent was included in the investigation. The PAH sorption and retention capabilities of the three fibers were determined through batch and continuous-flow experiments under non-competitive and competitive conditions. In the batch experiments, cattail fiber was the most effective sorbent. Kapok fiber provided the lowest PAH retention, while cattail fiber had slightly less PAH retention than polyester fiber. When two PAHs were present in the same system, a competitive effect on the much less hydrophobic PAH was observed. Similar results were obtained in the column experiments, except that polyester fiber performed much poorer on naphthalene. Cattail fiber is a promising sorbent for treating PAH-contaminated water, such as urban runoff.

  2. Sequential extraction of polycyclic aromatic hydrocarbons using subcritical water.

    PubMed

    Latawiec, Agnieszka E; Reid, Brian J

    2010-02-01

    A rapid sequential subcritical (superheated) water extraction method for polycyclic aromatic hydrocarbons (PAHs) in contaminated soil and sediment is presented. Decreasing the polarity of water by successive increase of the extraction temperature from 50 degrees C to 200 degrees C at the moderate pressure (10.3MPa) enabled selective, non-exhaustive extractions to be performed. Concurrent with increasing temperatures to 150 degrees C there was an increase in PAH extraction efficiencies. For the majority of determinations no significant differences between extractions at 150 degrees C and 200 degrees C were observed. Varied extraction efficiencies of PAHs at the same extraction conditions reflected dissimilarities between environmental matrices investigated. Selective subcritical water extraction of PAHs was proportional to their octanol-water partition coefficients. This technique may be applicable in evaluation of risks associated with PAH contaminated sites and in assessments of their bioremediation potential.

  3. Determination of polycyclic aromatic hydrocarbons in roasted coffee.

    PubMed

    Jimenez, Angelica; Adisa, Afolabi; Woodham, Cara; Saleh, Mahmoud

    2014-01-01

    Polycyclic aromatic hydrocarbons (PAHs) are suspected to be carcinogenic and mutagenic. This study describes the presence of PAHs in light, medium and dark roasted coffee including instant and decaffeinated brands. Total PAHs concentration was related to the degree of roasting with light roasted coffee showing the least and dark roasted coffee showing the highest level. Both instant and decaffeinated coffee brand showed lower levels of PAHs. Naphthalene, acenaphthylene, pyrene and chrysene were the most abundant individual isomers. The concentrations ranged from 0 to 561 ng g(-1) for naphthalene, 0 to 512 ng g(-1) for acenaphthylene, 60 to 459 ng g(-1) for pyrene and 56 to 371 ng g(-1) for chrysene. Thus, roasting conditions should be controlled to avoid the formation of PAHs due to their suspected carcinogenic and mutagenic properties.

  4. Simulated transport of polycyclic aromatic hydrocarbons in artificial streams

    SciTech Connect

    Bartell, S.M.; Landrum, P.F.; Giesy, J.P.; Leversee, G.J.

    1981-01-01

    A model was constructed to predict the pattern of flow and accumulation of three polycyclic aromatic hydrocarbons (PAH) (anthracene, naphthalene, and benzo(a)pyrene) in artificial streams located on the Savannah River Plant near Aiken, South Carolina. Predictions were based upon the premise that the fundamental chemistry of individual PAH contains useful information for predictive purposes. Model processes included volatilization, photolysis, sorption to sediments and particulates, and net accumulation by biota. Simulations of anthracene transport were compared to results of an experiment conducted in the streams. The model realistically predicted the concentration of dissolved anthracene through time and space. Photolytic degradation appeared to be a major pathway of anthracene flux from the streams.

  5. Extraction of polycyclic aromatic hydrocarbons from spiked soil

    SciTech Connect

    Coover, M.P.; Sims, R.C.; Doucette, W.

    1987-11-01

    A homogenization method was evaluated for extracting polycyclic aromatic hydrocarbons (PAHs) from soils. Fifteen PAHs were spiked and recovered from 2 soils at concentrations ranging from 1 to 1000 micrograms/g, using the homogenization method and a Soxhlet extraction method. Each extraction method performed well in removing the 15 PAHs from both soils over a broad range of concentrations. In general, Soxhlet extraction yielded slightly but significantly (P less than 0.05) higher recoveries than did the homogenization method. The homogenization method, however, was easy to use, and the extraction step turnaround time was less than 15 min/sample. The method should be suitable for other applications requiring the extraction of hydrophobic organic compounds from soils.

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

    PubMed

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

    2016-05-15

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

  7. Assessment of honey contamination with polycyclic aromatic hydrocarbons.

    PubMed

    Ciemniak, Artur; Witczak, Agata; Mocek, Kamila

    2013-01-01

    The aim of this study was to assess honey contamination by polycyclic aromatic hydrocarbons. Six species of honey were examined, as well as rape blossom and soil from villages Pęczerzyno and Przybysław in West Pomerania, Poland. The instrumental analysis was performed using a HP 6890 gas chromatograph coupled to a HP 5973 mass spectrometer with selected ion monitoring (SIM). Quantification was done by gas chromatography-mass spectrometry (GC-MS) using perdeuterated internal standards. Both soil samples showed high levels of all 23 PAHs, whereas honey contained mostly non-carcinogenic PAHs of low molecular weight. The most contaminated honey from Pęczerzyno contained 0.24 μg kg-1 benzo[a]pyrene. Moreover, despite low contamination of honey, a positive correlation was found between PAH content in honey, blossom and soil.

  8. Determination of polycyclic aromatic hydrocarbons in roasted coffee

    PubMed Central

    JIMENEZ, ANGELICA; ADISA, AFOLABI; WOODHAM, CARA; SALEH, MAHMOUD

    2016-01-01

    Polycyclic aromatic hydrocarbons (PAHs) are suspected to be carcinogenic and mutagenic. This study describes the presence of PAHs in light, medium and dark roasted coffee including instant and decaffeinated brands. Total PAHs concentration was related to the degree of roasting with light roasted coffee showing the least and dark roasted coffee showing the highest level. Both instant and decaffeinated coffee brand showed lower levels of PAHs. Naphthalene, acenaphthylene, pyrene and chrysene were the most abundant individual isomers. The concentrations ranged from 0 to 561 ng g−1 for naphthalene, 0 to 512 ng g−1 for acenaphthylene, 60 to 459 ng g−1 for pyrene and 56 to 371 ng g−1 for chrysene. Thus, roasting conditions should be controlled to avoid the formation of PAHs due to their suspected carcinogenic and mutagenic properties. PMID:25190557

  9. Health risks of residential exposure to polycyclic aromatic hydrocarbons.

    PubMed

    Brender, Jean D; Pichette, Janet L; Suarez, Lucina; Hendricks, Katherine A; Holt, Mandy

    2003-02-01

    A disease prevalence study and follow-up health surveillance were conducted among residents of an African-American community situated at the site of a former creosote wood-treatment facility contaminated with polycyclic aromatic hydrocarbons. Household interviews were conducted among 214 residents living around the hazardous waste site (target population) and 212 comparison residents in a neighborhood 2.4 km away from the site. Target area residents reported a higher prevalence of skin rashes than comparison residents (relative risk [RR] = 5.7; 95% confidence interval [CI] = 3.0, 10.9). The prevalence of reported rashes increased with increasing levels of anthracene detected in yards (test for linear trend, p = 0.02). With adjustment for environmental worry, reports of chronic bronchitis and difficulties becoming pregnant did not differ significantly between target and comparison residents (p > 0.05).

  10. Toxicological profile for polycyclic aromatic hydrocarbons. Final report

    SciTech Connect

    Not Available

    1990-12-01

    The ATSDR Toxicological Profile for Polycyclic Aromatic Hydrocarbons (PAHs): Acenaphthene, Acenaphthylene, Anthracene, Benzo(a)anthracene, Benzo(a)pyrene, Benzo(b)fluoranthene, Benzo(g,h,i)perylene, Benzo(k)fluoranthene, Chrysene, Dibenzo(a,h)anthracene, Fluoranthene, Fluorene, Indeno(1,2,3-cd)pyrene, Phenanthrene, Pyrene is intended to characterize succinctly the toxicological and health effects information for the substance. It identifies and reviews the key literature that describes the substance's toxicological properties. Other literature is presented but described in less detail. The profile begins with a public health statement, which describes in nontechnical language the substance's relevant toxicological properties. The adequacy of information to determine the substance's health effects is described. Research gaps in nontoxic and health effects information are described. Research gaps that are of significance to the protection of public health will be identified in a separate effort. The focus of the document is on health and toxicological information.

  11. Polycyclic Aromatic Hydrocarbons and the Diffuse Interstellar Bands: a Survey

    NASA Technical Reports Server (NTRS)

    Salama, F.; Galazutdinov, G. A.; Krelowski, J.; Allamandola, L. J.; Musaev, F. A.; DeVincenzi, Donald L. (Technical Monitor)

    1999-01-01

    We discuss the proposal relating the origin of some of the diffuse interstellar bands (DIBs) to neutral and ionized polycyclic aromatic hydrocarbons (PAHs) present in interstellar clouds. Laboratory spectra of several PAHs, isolated at low temperature in inert gas matrices, are compared with an extensive set of astronomical spectra of reddened, early type stars. From this comparison, it is concluded that PAN ions are good candidates to explain some of the DIBs. Unambiguous assignments are difficult, however, due to the shift in wavelengths and the band broadening induced in the laboratory spectra by the solid matrix. Definitive band assignments and, ultimately, the test of the of the proposal that PAH ions carry some of the DIB must await the availability of gas-phase measurements in the laboratory. The present assessment offers a guideline for future laboratory experiments by allowing the preselection of promising PAH molecules to be studied in jet expansions.

  12. Accumulation of polycyclic aromatic hydrocarbons (PAHs) in an urban snowpack.

    PubMed

    Boom, A; Marsalek, J

    1988-08-01

    Accumulations of polycyclic aromatic hydrocarbons in a snowpack were studied in an industrial urban area with numerous anthropogenic sources of PAHs. Average PAH loadings stored in the snowpack were determined, plotted on a map of the study area, and arenal distribution approximated by isoloading contours. The loading contours exhibited a marked elongation in the direction of prevailing winds. The unit-area deposition rates observed in the study area exceeded the typical rates reported for other urban areas, and were the highest immediately downwind of a steel plant. PAH levels in snowmelt were well below the freshwater aquatic life toxicity criteria, but exceeded both the WHO drinking water standard and the U.S. EPA carcinogenic criteria at the 10(-5) risk level.

  13. Transport of Polycyclic Aromatic Hydrocarbons in Unsaturated Porous Media

    NASA Astrophysics Data System (ADS)

    Chahal, Maninder; Flury, Markus

    2016-04-01

    Polycyclic aromatic hydrocarbons (PAHs) are complex organic molecules containing 2 or more fused benzene rings. Being hydrophobic and non-polar, PAHs tend to partition to the organic matter in the soil from bulk aqueous phase. Though transport of these contaminants has been well studied in saturated environment, interactive mechanisms of these fluorescent compounds in unsaturated (identified by presence of air-water interface) porous media is still not well understood. We studied is the transport of fluoranthene in unsaturated porous media as facilitated by moving air-water interfaces. Confocal microscopy was used to visualize the interactions of fluoranthene particles in a glass channel packed with quartz glass beads. The packed glass channel was used to mimic a porous media and effects of an advancing and receding capillary fringe on the detachment of fluoranthene.

  14. Emission factors for polycyclic aromatic hydrocarbons from biomass burning

    SciTech Connect

    Jenkins, B.M.; Jones, A.D.; Turn, S.Q.; Williams, R.B.

    1996-08-01

    Emission factors for 19 polycyclic aromatic hydrocarbons were measured during wind tunnel simulations of open burning for agricultural and forest biomass fuels including cereal grasses, agricultural tree prunings, and fir and pine wood (slash). Yields of total PAH varied from 5 to 683 mg kg{sup -1} depending principally on burning conditions and to a lesser extent on fuel type. Barley straw and wheat straw loaded at 400-500 g m{sup -2} emitted much higher levels of PAH, including benzo[a]pyrene, than other cereal and wood fuel types burning under more robust conditions. As anticipated, total PAH emission rates increased with increasing particulate matter emission rates and with declining combustion efficiency. 20 refs., 2 figs., 6 tabs.

  15. Phototoxicity of polycyclic aromatic hydrocarbons at varying light intensities

    SciTech Connect

    Ankley, G.T.; Phipps, G.L.; Mattson, V.R.; Erickson, R.J.; Kosian, P.A.; Cox, J.S.; Sheedy, B.R.; Mount, D.R.

    1994-12-31

    Conceptual models suggest that the toxicity of photoactivated polycyclic aromatic hydrocarbons (PAHs) should be a function both of chemical (PAH) dose, and intensity of the ultraviolet (UV) light to which the organism is exposed (photon dose). However, there have been no systematic studies with aquatic organisms to quantify the relationship between PAH dose and UV intensity in producing phototoxicity. In these studies, oligochaetes (Lumbriculus variegatus) were exposed, via the water, to multiple concentrations of individual PAHs known to be photoactivated (fluoranthene, pyrene, anthracene), and then placed under UV light of three different intensities. The resultant phototoxicity clearly was a function both of PAH dose and light intensity. A joint toxicity model relating toxicity to PAH concentrations and light intensity will be presented.

  16. Metabolism of polycyclic aromatic hydrocarbons in the aquatic environment

    SciTech Connect

    Varanasi, U.

    1989-01-01

    During the past decade, knowledge of polycyclic aromatic hydrocarbons (PAH) in the aquatic environment has advanced substantially to encompass studies of bioavailability, metabolism, subsequent toxic effects, and their ecological consequences. In this book, recent advances in the areas of PAH biogeochemistry and bioaccumulation, microbial degradation, enzymes of activation and detoxication, metabolism of PAH, and laboratory and field studies on carcinogenic/toxic effects, are presented. Additionally, important similarities and differences in metabolism of PAH by aquatic and terrestrial organisms are discussed. These chapters also illustrate that although considerable progress has been made in certain areas of PAH metabolism in the aquatic environment, the field is relatively unexplored and many exciting possibilities exist for future investigations. Separate abstracts are included for 9 chapters in this book for inclusion in the appropriate data bases.

  17. Polycyclic aromatic hydrocarbons in fuel-oil contaminated soils, Antarctica.

    PubMed

    Aislabie, J; Balks, M; Astori, N; Stevenson, G; Symons, R

    1999-12-01

    Where fuel oil spills have occurred on Antarctic soils polycyclic aromatic hydrocarbons (PAH) may accumulate. Surface and subsurface soil samples were collected from fuel spill sites up to 30 years old, and from nearby control sites, and analysed for the 16 PAHs on the USEPA priority pollutants list, as well as for two methyl substituted naphthalenes, 1-methylnaphthalene and 2-methylnaphthalene. PAH levels ranged from 41-8105 ng g-1 of dried soil in the samples from contaminated sites and were below detection limits in control site samples. PAH were detected in surface soils and had migrated to lower depths in the contaminated soil. The predominant PAH detected were naphthalene and its methyl derivatives.

  18. In situ groundwater aeration of polycyclic aromatic hydrocarbons

    SciTech Connect

    Symons, B.D.; Linkenheil, R.; Pritchard, D.; Shanke, C.A.; Seep, D.

    1995-12-31

    At a former wood treating site in Minnesota, the feasibility of in situ groundwater aeration was investigated in a laboratory treatability setting, to evaluate biodegradability and optimal operation conditions of the site aquifer. After concluding that an aeration system would increase the dissolved oxygen concentrations in the groundwater enough to sustain microbial life, a field demonstration system was designed and installed. The system was operated for 1 year, during which groundwater quality at upgradient and downgradient wells was monitored to evaluate the system`s effectiveness. The groundwater aeration system successfully reduced groundwater polycyclic aromatic hydrocarbon (PAH) concentrations, especially naphthalene. Naphthalene concentrations were reduced from 1,319 {micro}g/L to below the laboratory detection limit of 0.5 {micro}g/L. Cumulative concentrations of other PAH compounds were reduced from 98 {micro}g/L to 23 {micro}g/L during the 1-year test.

  19. A review of polycyclic aromatic hydrocarbons (PAHs) research progress in China based on CNKI database

    NASA Astrophysics Data System (ADS)

    Zhang, Zhao

    2017-03-01

    This article using the retroactive content analysis method summarizes the research progress of air polycyclic aromatic hydrocarbons during 1983 to 2016, and is based on the 72 search results about "Air Polycyclic Aromatic Hydrocarbons" in CNKI database. This article directly points out the study achievements and improvements about air polycyclic aromatic hydrocarbons from 4 aspects, the reviews of the studies of PAHs in a special stage, the studies on PAHs determination and analysis method, the studies on PAHs concentration in different places and the studies on the relationship between PAHs concentration in air and human health, respectively.

  20. Thermochemical properties and phase behavior of halogenated polycyclic aromatic hydrocarbons.

    PubMed

    Fu, Jinxia; Suuberg, Eric M

    2012-03-01

    Knowledge of vapor pressure of organic pollutants is essential in predicting their fate and transport in the environment. In the present study, the vapor pressures of 12 halogenated polycyclic aromatic compounds (PACs), 9-chlorofluorene, 2,7-dichlorofluorene, 2-bromofluorene, 9-bromofluorene, 2,7-dibromofluorene, 2-bromoanthracene, 9-chlorophenanthrene, 9-bromophenanthrene, 9,10-dibromophenanthrene, 1-chloropyrene, 7-bromobenz[a]anthracene, and 6,12-dibromochrysene, were measured using the Knudsen effusion method over the temperature range of 301 to 464 K. Enthalpies and entropies of sublimation of these compounds were determined via application of the Clausius-Clapeyron equation. The data were also compared with earlier published literature values to study the influence of halogen substitution on vapor pressure of PACs. As expected, the halogen substitution decreases vapor pressure compared with parent compounds but does not necessarily increase the enthalpy of sublimation. Furthermore, the decrease of vapor pressure also depends on the substitution position and the substituted halogen, and the di-substitution of chlorine and/or bromine decreases the vapor pressure compared with single halogen-substituted polycyclic aromatic hydrocarbons. In addition, the enthalpy of fusion and melting temperature of these 12 PACs were determined using differential scanning calorimetry and melting point analysis.

  1. 14C Incorporation into the Fatty Acids and Aliphatic Hydrocarbons of Sarcina lutea

    PubMed Central

    Tornabene, T. G.; Oró, J.

    1967-01-01

    An initial investigation into the mechanism of hydrocarbon biosynthesis in Sarcina lutea was performed by measuring the amounts of 14C incorporated into the hydrocarbons and fatty acids by use of a combination gas chromatograph and high-temperature gas-flow ionization apparatus. Uniformly labeled l-isoleucine-14C was predominantly incorporated into the anteiso-branched chains. Palmitate-16-14C gave evidence that a direct correlation may exist between the nonpolar end of the palmitate and the biosynthesis of hydrocarbons and carotenoids. The label from palmitate-1-14C was incorporated into the various hydrocarbon groups as a compound, derived from the polar end of the palmitate, consisting of more than two carbon atoms. Palmitate-16-14C and -1-14C gave no detectable evidence that transformed products were incorporated into other fatty acids. Sodium acetate-2-14C and uniformly labeled l-leucine-14C gave evidence of a nonspecific incorporation into both the aliphatic hydrocarbons and fatty acids of Sarcina lutea. PMID:6039358

  2. The FEMA GRAS assessment of aliphatic and aromatic terpene hydrocarbons used as flavor ingredients.

    PubMed

    Adams, T B; Gavin, C Lucas; McGowen, M M; Waddell, W J; Cohen, S M; Feron, V J; Marnett, L J; Munro, I C; Portoghese, P S; Rietjens, I M C M; Smith, R L

    2011-10-01

    This publication is the thirteenth in a series of safety evaluations performed by the Expert Panel of the Flavor and Extract Manufacturers Association (FEMA). In 1993, the Panel initiated a comprehensive program to re-evaluate the safety of more than 1700 GRAS flavoring substances under conditions of intended use. Since then, the number of flavoring substances has grown to more than 2600 substances. Elements that are fundamental to the safety evaluation of flavor ingredients include exposure, structural analogy, metabolism, pharmacokinetics and toxicology. Flavor ingredients are evaluated individually and in the context of the available scientific information on the group of structurally related substances. Scientific data relevant to the safety evaluation of the use of aliphatic and aromatic terpene hydrocarbons as flavoring ingredients are evaluated. The group of aliphatic and aromatic terpene hydrocarbons was reaffirmed as GRAS (GRASr) based, in part, on their self-limiting properties as flavoring substances in food; their rapid absorption, metabolic detoxication, and excretion in humans and other animals; their low level of flavor use; the wide margins of safety between the conservative estimates of intake and the no-observed-adverse effect levels determined from subchronic and chronic studies and the lack of significant genotoxic potential.

  3. Polycyclic aromatic hydrocarbons (PAHs) in livers of California sea otters.

    PubMed

    Kannan, Kurunthachalam; Perrotta, Emily

    2008-03-01

    Concentrations of 16 polycyclic aromatic hydrocarbons (PAHs) were measured in livers of 81 adult female sea otters collected along the California coast in 1992-2002. Concentrations of summation operatorPAHs in livers of sea otters were in the range of 588-17400ng/g lipid wt (mean: 3880ng/g, lipid wt). On a wet weight basis, the concentrations ranged from 17 to 1430ng/g (mean: 146ng/g). Overall, di- and tri-cyclic aromatic hydrocarbons, namely, naphthalene, fluorene, phenanthrene/anthracene, and acenaphthylene, were the predominant compounds found in the livers. Although petroleum-related sources appear to be the major contributors to PAH exposure in sea otters, exposure sources varied by geographical sub-regions. Dibenz[a,h]anthracene was found to comprise a significant proportion of the summation operatorPAH concentrations in sea otters from the northern sub-region of the study area. No significant difference existed in the concentrations of summation operatorPAHs among sea otters that died from infectious diseases, emaciation, and noninfectious causes. Concentrations of summation operatorPAHs in livers of sea otters decreased significantly from 1992 to 2002. Because of the rapid metabolism of PAHs in marine mammals such as sea otters, further studies examining the association of PAHs with health effects should determine hydroxylated metabolites in livers.

  4. Thermodiffusion of polycyclic aromatic hydrocarbons in binary mixtures

    NASA Astrophysics Data System (ADS)

    Hashmi, Sara M.; Senthilnathan, Sid; Firoozabadi, Abbas

    2016-11-01

    Thermodiffusion in liquid mixtures may explain some counter-intuitive but naturally occurring phenomena such as hydrocarbon reservoirs with heavier component(s) stratified on top of lighter ones. However, beyond benchmark systems, systematic measurements of thermodiffusion in binary organic mixtures are lacking. We use an optical beam deflection apparatus to simultaneously probe Fickian and thermal diffusion in binary solution mixtures of polycyclic aromatic hydrocarbons dissolved in alkanes, and measure both Fickian diffusion D and the Soret coefficient ST, and then obtain the thermodiffusion coefficient DT. In a series of nine binary mixtures, we vary both the size of the aromatic compound from two to four rings, as well as the length of the alkane chain from 6 to 16 carbons. To probe the effect of increasing ring size, we include a 6-ringed aromatic compound, coronene, and toluene as a solvent, due to the insolubility of coronene in alkanes. Our results suggest that Fickian diffusion increases with the inverse of solvent viscosity and also with decreasing molecular weight of the solute. While both of these trends match our intuition, the behavior of ST and DT is more complicated. We find that ST and DT increase with the solute molecular weight when the solvent is held fixed and that the impact of solute ring size is higher in shorter chain alkane solvents.

  5. Diversity of metabolic capacities among strains degrading polycyclic aromatic hydrocarbons

    SciTech Connect

    Bouchez, M.; Besnaienou, B.; Blanchet, D.; Vandecasteele, J.P.

    1995-12-31

    Strains of Pseudomonas and Rhodococcus genera were isolated for their capacity to use, as a sole carbon and energy source, one of the following polycyclic aromatic hydrocarbons (PAHs): naphthalene (NAP), fluorene (FLU), phenanthrene (PHE), anthracene (ANT), fluoranthene (FLT), and pyrene (PYR). The range of PAHs supporting growth of these pure strains was usually restricted, but several other hydrocarbons were used by Rhodococcus sp. All strains could grow on simple organic acids. Maximal specific growth rates ({mu}{sub max}) of all strains on their PAH growth substrates were determined by respirometry. No clear relationships between {mu}{sub max} values and the molecular weight or water solubility of PAHs were apparent, but Pseudomonas sp. exhibited the highest {mu}{sub max} values. Carbon balances for PAH biodegradation were established. Differences between strains were observed, but high mineralization rates and low production of soluble metabolites were obtained for all PAHs. Bacterial biomass represented 16% to 35% of the carbon consumed. Strain diversity was also apparent in the interactions observed in the degradation of a mixture of two PAHs by individual strains, which often involved inhibition of PAH substrate degradation, with or without cometabolization of the second PAH.

  6. Variations in the 3 Micron Spectrum across the Orion Bar: Polycyclic Aromatic Hydrocarbons and Related Molecules

    NASA Astrophysics Data System (ADS)

    Sloan, G. C.; Bregman, J. D.; Geballe, T. R.; Allamandola, L. J.; Woodward, E.

    1997-01-01

    Long-slit spectra across the Orion Bar reveal significant differences in the spatial behavior of the components of the 3 μm polycyclic aromatic hydrocarbon (PAH) spectrum. The strong PAH band at 3.29 μm generally decreases exponentially with distance from the ionization front into the molecular cloud (scale height ~12"), although excesses appear ~10" and ~20" behind the ionization front, close to layers of H2 and CO emission, respectively. The 3.40 μm PAH feature separates into two components with very different spatial distributions. The main component (at 3.395 μm), along with the 3.51 μm band and the PAH plateau (3.3-3.6 μm), shows excess emission ~10" and ~20" behind the ionization front, stronger than the excesses in the 3.29 μm band. The extra component of the 3.40 μm band, which peaks at ~3.405 μm, has a spatial distribution very similar to the H2 emission. Aromatic C--H stretches in PAHs most likely produce the 3.29 μm feature. Aliphatic C--H stretches in either attached methyl sidegroups or superhydrogenated PAHs, or perhaps both, could produce the complicated spectral and spatial structure at 3.40 μm.

  7. Variations in the 3 micron spectrum across the Orion Bar: polycyclic aromatic hydrocarbons and related molecules

    NASA Technical Reports Server (NTRS)

    Sloan, G. C.; Bregman, J. D.; Geballe, T. R.; Allamandola, L. J.; Woodward, C. E.

    1997-01-01

    Long-slit spectra across the Orion Bar reveal significant differences in the spatial behavior of the components of the 3 microns polycyclic aromatic hydrocarbon (PAH) spectrum. The strong PAH band at 3.29 microns generally decreases exponentially with distance from the ionization front into the molecular cloud (scale height approximately 12"), although excesses appear approximately 10" and 20" behind the ionization front, close to layers of H2 and CO emission, respectively. The 3.40 microns PAH feature separates into two components with very different spatial distributions. The main component (at 3.395 microns), along with the 3.51 microns band and the PAH plateau (3.3-3.6 microns), shows excess emission approximately 10" and approximately 20" behind the ionization front, stronger than the excesses in the 3.29 microns band. The extra component of the 3.40 microns band, which peaks at approximately 3.405 microns, has a spatial distribution very similar to the H2 emission. Aromatic C-H stretches in PAHs most likely produce the 3.29 microns feature. Aliphatic C-H stretches in either attached methyl side-groups or superhydrogenated PAHs, or perhaps both, could produce the complicated spectral and spatial structure at 3.40 microns.

  8. Polyethylene-water partitioning coefficients for parent- and alkylated-polycyclic aromatic hydrocarbons and polychlorinated biphenyls.

    PubMed

    Choi, Yongju; Cho, Yeo-Myoung; Luthy, Richard G

    2013-07-02

    We report polyethylene (PE)-water partitioning coefficients (K(PE)) for 17 parent-polycyclic aromatic hydrocarbons (PAHs), 22 alkylated-PAHs, 3 perdeuterated parent-PAHs, and 100 polychlorinated biphenyl (PCB) congeners or coeluting congener groups. The K(PE) values for compounds in the same homologue group are within 0.2 log units for alkylated-PAHs but span up to an order of magnitude for PCBs, due to the greater contribution of the position of the substituents (i.e., chlorines for PCBs and alkyl groups for alkylated-PAHs) to the molecular structure. The K(PE) values in deionized water for parent- and alkylated-PAHs show a good correlation with a regression model employing the number of aromatic carbons (C(AR)) and aliphatic carbons (C(AL)) in each compound: log K(PE) = -0.241 + 0.313 C(AR) + 0.461 C(AL). The regression model is useful for the assessment of freely dissolved aqueous concentrations of alkylated-PAHs, which comprise a significant fraction of the total in petroleum-derived PAHs and in some pyrogenic PAH mixtures. For PCBs, experimentally determined octanol-water partitioning coefficients are the best predictor of the K(PE) values among the molecular parameters studied. The effect of salinity up to 20 or 30 parts per thousand is found to be relatively insignificant on K(PE) values for PAHs or PCBs, respectively.

  9. ASSAYING PARTICLE-BOUND POLYCYCLIC AROMATIC HYDROCARBONS (PAH) FROM ARCHIVED PM2.5 FILTERS

    EPA Science Inventory

    Airborne particulate matter contains numerous organic species, including several polycyclic aromatic hydrocarbons (PAHs) that are known or suspected carcinogens. Existing methods for measuring airborne PAHs are complex and costly, primarily because they are designed to collect...

  10. STUDIES ON BIOREMEDIATION OF POLYCYCLIC AROMATIC HYDROCARBON-CONTAMINATED SEDIMENTS: BIOAVAILABILITY, BIODEGRADABILITY, AND TOXICITY ISSUES

    EPA Science Inventory

    The widespread contamination of aquatic sediments by polycyclic aromatic hydrocarbons (PAHs) has created a need for cost-effective bioremediation processes, on which the bioavailability and the toxicity of PAHs often have a significant impact. This research investigated the biode...

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

    EPA Science Inventory

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

  12. MULTISUBSTRATE BIODEGRADATION KINETICS FOR BINARY AND COMPLEX MIXTURES OF POLYCYCLIC AROMATIC HYDROCARBONS

    EPA Science Inventory

    Biodegradation kinetics were studied for binary and complex mixtures of nine polycyclic aromatic hydrocarbons (PAHs): naphthalene, 1-methylnaphthalene, 2-methylnaphthalene, 2-ethylnaphthalene, phenanthrene, anthracene, pyrene, fluorene and fluoranthene. Discrepancies between the ...

  13. PHOTOACTIVATION AND TOXICITY OF MIXTURES OF POLYCYCLIC AROMATIC HYDROCARBON COMPOUNDS IN MARINE SEDIMENT

    EPA Science Inventory

    The direct toxicity and photoinduced toxicity of sediment-associated acenaphthene, phenanthrene, fluoranthene, and pyrene were determined for the marine amphipod Rhepoxynius abronius. The four polycyclic aromatic hydrocarbons (PAHs) were spiked into sediment in a concentration se...

  14. Webinar Presentation: Prenatal Exposures to Polycyclic Aromatic Hydrocarbons (PAH) and Childhood Body Mass Index Trajectories

    EPA Pesticide Factsheets

    This presentation, Prenatal Exposures to Polycyclic Aromatic Hydrocarbons (PAH) and Childhood Body Mass Index Trajectories, was given at the NIEHS/EPA Children's Centers 2015 Webinar Series held on Feb. 11, 2015.

  15. Modeling the Role of Alkanes, Polycyclic Aromatic Hydrocarbons, and Their Oligomers in Secondary Organic Aerosol Formation

    EPA Science Inventory

    A computationally efficient method to treat secondary organic aerosol (SOA) from various length and structure alkanes as well as SOA from polycyclic aromatic hydrocarbons (PAHs) is implemented in the Community Multiscale Air Quality (CMAQ) model to predict aerosol concentrations ...

  16. Do lagoon area sediments act as traps for polycyclic aromatic hydrocarbons?

    PubMed

    Marini, Mauro; Frapiccini, Emanuela

    2014-09-01

    The coastal lagoons are vulnerable systems, located between the land and the sea, enriched by both marine and continental inputs and are among the most productive aquatic ecosystems. The purpose of this work is to understand the influence of the lagoon area sediments on the behaviour of polycyclic aromatic hydrocarbons, through the adsorption coefficient determination. In fact, the sorption of polycyclic aromatic hydrocarbons is an important process because it governs the fate, transport, bioavailability and toxicity of these compounds in sediments. It has been observed that the adsorption of polycyclic aromatic hydrocarbons in a transitional system is the outcome of different factors, such as their sources and physicochemical properties, salinity and sediment composition, hydrology and environmental conditions. The results showed that transitional areas contribute to the polycyclic aromatic hydrocarbon accumulation in the sediment turning it into a trap.

  17. COMPUTATIONAL METHODS FOR STUDYING THE INTERACTION BETWEEN POLYCYCLIC AROMATIC HYDROCARBONS AND BIOLOGICAL MACROMOLECULES

    EPA Science Inventory

    Computational Methods for Studying the Interaction between Polycyclic Aromatic Hydrocarbons and Biological Macromolecules .

    The mechanisms for the processes that result in significant biological activity of PAHs depend on the interaction of these molecules or their metabol...

  18. Sources and pathways of polycyclic aromatic and saturated hydrocarbons in the Arkona Basin (Southern Baltic Sea, Central Europe)

    SciTech Connect

    Schulz, H.M.

    1996-12-31

    The Baltic Sea (Central Europe) is surrounded by coastal regions with long histories of industrialization. The heavy metal profiles in the sediments in the center of the Arkona Basin, one of the depressions of the southern Baltic Sea area, clearly reflect the historical anthropogenic influence. The Arkona Basin-is the final sink for materials derived from the Oder river which drains a highly polluted industrial area of Eastern Europe. Surficial muddy sediments from a close-meshed field of sampling-points were analyzed for distribution patterns of aliphatics and quantities and ratios of selected polycyclic aromatic hydrocarbons (PAH). These compounds are thought to reflect anthropogenic pollution related to emissions from traffic, heating, etc. We use these marker substances to test if the basin sediments reflect riverine input, and if additional sources can be identified.

  19. Sources and distribution of aliphatic and polyaromatic hydrocarbons in coastal sediments from the Ushuaia Bay (Tierra del Fuego, Patagonia, Argentina).

    PubMed

    Commendatore, Marta G; Nievas, Marina L; Amin, Oscar; Esteves, José L

    2012-03-01

    The environmental quality of Ushuaia Bay, located at the southernmost tip of South America, is affected by the anthropogenic pressure of Ushuaia city. In this study, levels and sources of hydrocarbons in coastal sediments were assessed. Aliphatic hydrocarbon fractions ranged between 5.5 and 1185.3 μg/g dry weight and PAHs from not detected to 360 ng/g. Aliphatic diagnostic indices, the nalkanes homologous series occurrence, Aliphatic Unresolved Complex Mixtures (AliUCMs), and pristane and phytane isoprenoids indicated a petrogenic input. Some sites showed biogenic features masked by the anthropogenic signature. Particularly in port areas biodegradation processes were evident. PAH ratios showed a mixture of petrogenic and pyrogenic sources. Aliphatic and aromatic UCMs were strongly correlated, reflecting chronic pollution. Three areas were distinguished inside the bay: (1) east, with low hydrocarbons impact; (2) central, where hydrocarbons accumulation was related to source proximity and sediment characteristics; (3) south-west, where sediment characteristics and current circulation favour hydrocarbons accumulation.

  20. Carbon isotope systematics of individual hydrocarbons in hydrothermal petroleum from Escanaba Trough, Northeastern Pacific Ocean

    USGS Publications Warehouse

    Simoneit, B.R.T.; Schoell, M.; Kvenvolden, K.A.

    1997-01-01

    We submitted individual aliphatic and polycyclic aromatic hydrocarbons in samples of hydrothermal petroleum from Escanaba trough to compound specific isotope analysis to trace their origins. The carbon isotope compositions of the alkanes and polycyclic aromatic hydrocarbons (means -27.5 and -24.7%, respectively) reflect a primarily terrestrial organic matter source.We submitted individual aliphatic and polycyclic aromatic hydrocarbons in samples of hydrothermal petroleum from Escanaba Trough to compound specific isotope analysis to trace their origins. The carbon isotope compositions of the alkanes and polycyclic aromatic hydrocarbons (means -27.5 and -24.7 per mill, respectively) reflect a primarily terrestrial organic matter source.

  1. Emission of polycyclic aromatic hydrocarbons from gasohol and ethanol vehicles

    NASA Astrophysics Data System (ADS)

    de Abrantes, Rui; Vicente de Assunção, João; Pesquero, Célia Regina; Bruns, Roy Edward; Nóbrega, Raimundo Paiva

    The exhaust emission of the polycyclic aromatic hydrocarbons (PAHs) considered toxic to human health were investigated on two spark ignition light duty vehicles, one being gasohol (Gasohol, in Brazil, is the generic denomination for mixtures of pure gasoline plus 20-25% of anhydrous ethyl alcohol fuel (AEAF).)-fuelled and the other a flexible-fuel vehicle fuelled with hydrated ethanol. The influence of fuel type and quality, aged lubricant oil type and use of fuel additives on the formation of these compounds was tested using standardized tests identical to US FTP-75 cycle. PAH sampling and chemical analysis followed the basic recommendations of method TO-13 (United States. Environmental Protection Agency, 1999. Compendium Method TO-13A - Determination of polycyclic Aromatic hydrocarbons (PAH) in Ambient Air Using Gas Chromatography/Mass Spectrometry (CG/MS). Center for environmental research information, Cincinnati, p. 78), with the necessary modification for this particular application. Results showed that the total PAH emission factor varied from 41.9 μg km -1 to 612 μg km -1 in the gasohol vehicle, and from 11.7 μg km -1 to 27.4 μg km -1 in the ethanol-fuelled vehicle, a significant difference in favor of the ethanol vehicle. Generally, emission of light molecular weight PAHs was predominant, while high molecular weights PAHs were not detected. In terms of benzo( a)pyrene toxicity equivalence, emission factors varied from 0.00984 μg TEQ km -1 to 4.61 μg TEQ km -1 for the gasohol vehicle and from 0.0117 μg TEQ km -1 to 0.0218 μg TEQ km -1 in the ethanol vehicle. For the gasohol vehicle, results showed that the use of fuel additive causes a significant increase in the emission of naphthalene and phenanthrene at a confidence level of 90% or higher; the use of rubber solvent on gasohol showed a reduction in the emission of naphthalene and phenanthrene at the same confidence level; the use of synthetic oil instead of mineral oil also contributed

  2. Source apportionment of sediment-associated aliphatic hydrocarbon in a eutrophicated shallow lake, China.

    PubMed

    Wang, Ji-Zhong; Yang, Ze-Yu; Chen, Tian-Hu

    2012-11-01

    Chaohu Lake, one of the most eutrophicated lakes in China, has been suffering from long-term outside pollution, urban sewage, river outflows, and agricultural runoff which expectedly have been the main contributors of hydrocarbons. However, the contributions from these various sources have not been specified. The present study is aimed at identifying the potential sources of hydrocarbons in surface sediment around the whole lake and assessing the relative contributions using principal components analysis-multiple linear regression (PCA-MLR). Sixty-one surface sediments covering the whole Chaohu Lake and three main estuaries of inflowing rivers were collected, dried, extracted, and analyzed for 27 normal alkanes (n-alkanes, from C(12) to C(38), defined Σ(27)AH) and unresolved complex mixture (UCM) by GC/MS. Diagnostic ratios and PCA-MLR were utilized to apportion their sources. The concentrations of Σ(27)AH and UCM ranged from 434 to 3,870 ng/g and 11.9 to 325 μg/g dry weight, respectively, for all samples. The concentrations of Σ(27)AH in western region and estuary of Nanfei River were slightly higher but without statistical significance than those from eastern region and estuaries of Yuxi River and Hangbu River. The concentration of UCM from western region was significantly higher than that obtained from eastern region. These results reflect the importance of input of urban runoff by Nanfei River and serious eutrophication in western region. Aliphatic hydrocarbons in Chaohu Lake were mainly derived from high plant wax with mixed sources of phytoplankton and petroleum. Weak microbial decomposition of n-alkanes would be expected to occur from the low ratios of isoprenoid hydrocarbons pristine (pri) and phytane (phy) to n-C(17) and n-C(18), respectively. Higher plant, fossil combustion, petroleum residue, and phytoplankton were proposed as the main origines of aliphatic hydrocarbons by PCA while the contributions of individual n-alkane homologues, pri and phy

  3. The galactic distribution of aliphatic hydrocarbons in the diffuse interstellar medium

    NASA Technical Reports Server (NTRS)

    Sandford, Scott A.; Pendleton, Yvonne J.; Allamandola, Louis J.

    1995-01-01

    The infrared absorption feature near 2950(exp -1) (3.4 micron), characteristic of dust in the diffuse interstellar medium (ISM), is attributed to C-H stretching vibrations of aliphatic hydrocarbons. We show here that the strength of the band does not scale linearly with visual extinction everywhere, but instead increases more rapidly for objects near the center of the Galaxy, a behavior that parallels that of the Si-O stretching band due to silicate materials in the diffuse ISM. This implies that the grains responsible for the diffuse medium aliphatic C-H and silicate Si-O stretching bands are different from those responsible for much of the observed visual extinction. It also suggests that the distribution of the carbonaceous component of the diffuse ISM is not uniform throughout the Galaxy, but instead may increase in density toward the center of the Galaxy. The similar behavior of the C-H and Si-O stretching bands suggests that these two components may be coupled, perhaps in the form of silicate-core, organic-mantle grains. Several possible models of the distribution of this material are presented and it is demonstrated that the inner parts of the Galaxy has a carrier density that is 5 to 35 times higher than in the local ISM. Depending on the model used, the density of aliphatic material in the local ISM is found to be about 1 to 2 -CH3 groups m(exp -3) and about 2 to 5 -CH2- groups m(exp -3). These densities are consistent with the strengths of the 2955 and 2925 cm(exp -1) (3.4 micron) band being described by the relations A(sub nu)/tau(sub 2955 cm(exp -1)) = 270 +/- 40 and A(sub nu)/tau(sub 2925 cm(exp -1)) = 250 +/- 40 in the local diffuse ISM.

  4. Partition characteristics of polycyclic aromatic hydrocarbons on soils and sediments

    USGS Publications Warehouse

    Chiou, C.T.; Mcgroddy, S.E.; Kile, D.E.

    1998-01-01

    The partition behavior was determined for three polycyclic aromatic hydrocarbons (PAHs), i.e., naphthalene, phenanthrene, and pyrene, from water to a range of soil and sediment samples. The measured partition coefficients of the individual PAHs between soil/sediment organic matter (SOM) and water (i.e., K(oc) values) are relatively invariant either for the 'clean' (uncontaminated) soils or for the clean sediments; however, the mean K(oc) values on the sediments are about twice the values on the soils. This disparity is similar to the earlier observation for other nonpolar solutes and reflects the compositional differences between soil and sediment organic matters. No significant differences in K(oc) are observed between a clean coastal marine sediment and freshwater sediments. The coastal sediments that are significantly impacted by organic contaminants exhibit higher K(oc) values. At given K(ow) values (octanol-water), the PAHs exhibit much higher K(oc) values than other relatively nonpolar solutes (e.g., chlorinated hydrocarbons). This effect is shown to result from the enhanced partition of PAHs to SOM rather than from lower K(ow) values of PAHs at given supercooled liquid solute solubilities in water. The enhanced partition of PAHs over other nonpolar solutes in SOM provides an account of the markedly different correlations between log K(oc) and log K(ow) for PAHs and for other nonpolar solutes. The improved partition of PAHs in SOM stems apparently from the enhanced compatibility of their cohesive energy densities with those of the aromatic components in SOM. The approximate aromatic fraction in soil/sediment organic matter has been assessed by solid-state 13C-NMR spectroscopy.The partition behavior was determined for three polycyclic aromatic hydrocarbons (PAHs), i.e., naphthalene, phenanthrene, and pyrene, from water to a range of soil and sediment samples. The measured partition coefficients of the individual PAHs between soil/sediment organic matter (SOM

  5. Aliphatic and aromatic hydrocarbons in different sized aerosols over the Mediterranean Sea: Occurrence and origin

    NASA Astrophysics Data System (ADS)

    Sicre, M. A.; Marty, J. C.; Saliot, A.; Aparicio, X.; Grimalt, J.; Albaiges, J.

    Marine aerosols were collected using a five-stage cascade impactor during the PHYCEMED II cruise in the Western Mediterranean Sea (October 1983). Their composition in aliphatic and aromatic hydrocarbons (HCs) was analyzed, representing the first time that concentrations of polynuclear aromatic HCs (PAH) are reported in relation to particle size for aerosols of remote marine areas. The HC concentrations were found to be dependent on the origin of the air masses. They were higher for air coming from North European countries than for air originating in the Atlantic and the South of Spain. The concentrations range between 7 and 14 ng m -3for n-alkanes and between 0.2 and 0.4 ng m -3for total PAH. Based on molecular criteria, several sources for these HCs have been identified: continental higher plant waxes, petroleum and pyrolysis (namely coal combustion and vehicular exhausts). Mass medium equivalent diameters (MMED) for the naturally derived n-alkanes are in the 1.79-2.53 μm range, indicating an origin related with the emission of large particles from higher plant waxes or from soil dusts. In contrast, MMED for the anthropogenic HCs, both aliphatic and aromatic, are smaller than the micron, suggesting initial emission of PAH through pyrolytic processes in the vapor phase followed by condensation onto larger sub-μm particles.

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

    NASA Astrophysics Data System (ADS)

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

    2016-08-01

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

  7. Polycyclic aromatic hydrocarbons: from metabolism to lung cancer.

    PubMed

    Moorthy, Bhagavatula; Chu, Chun; Carlin, Danielle J

    2015-05-01

    Excessive exposure to polycyclic aromatic hydrocarbons (PAHs) often results in lung cancer, a disease with the highest cancer mortality in the United States. After entry into the lung, PAHs induce phase I metabolic enzymes such as cytochrome P450 (CYP) monooxygenases, i.e. CYP1A1/2 and 1B1, and phase II enzymes such as glutathione S-transferases, UDP glucuronyl transferases, NADPH quinone oxidoreductases (NQOs), aldo-keto reductases (AKRs), and epoxide hydrolases (EHs), via the aryl hydrocarbon receptor (AhR)-dependent and independent pathways. Humans can also be exposed to PAHs through diet, via consumption of charcoal broiled foods. Metabolism of PAHs through the CYP1A1/1B1/EH pathway, CYP peroxidase pathway, and AKR pathway leads to the formation of the active carcinogens diol-epoxides, radical cations, and o-quinones. These reactive metabolites produce DNA adducts, resulting in DNA mutations, alteration of gene expression profiles, and tumorigenesis. Mutations in xenobiotic metabolic enzymes, as well as polymorphisms of tumor suppressor genes (e.g. p53) and/or genes involved in gene expression (e.g. X-ray repair cross-complementing proteins), are associated with lung cancer susceptibility in human populations from different ethnicities, gender, and age groups. Although various metabolic activation/inactivation pathways, AhR signaling, and genetic susceptibilities contribute to lung cancer, the precise points at which PAHs induce tumor initiation remain unknown. The goal of this review is to provide a current state-of-the-science of the mechanisms of human lung carcinogenesis mediated by PAHs, the experimental approaches used to study this complex class of compounds, and future directions for research of these compounds.

  8. Reflectance spectroscopy (350-2500 nm) of solid-state polycyclic aromatic hydrocarbons (PAHs)

    NASA Astrophysics Data System (ADS)

    Izawa, M. R. M.; Applin, D. M.; Norman, L.; Cloutis, E. A.

    2014-07-01

    Polycyclic aromatic hydrocarbons (PAHs) are organic compounds based on fused aromatic rings, and are formed in a variety of astrophysical, solar nebula and planetary processes. Polycyclic aromatic hydrocarbons are known or suspected to occur in a wide variety of planetary settings including icy satellites, Titan’s hazes, carbonaceous meteorites, comet nuclei, ring particles; and terrestrial organic-rich lithologies such as coals, asphaltites, and bituminous sands. Relatively few measurements of the visible and near-infrared spectra of PAHs exist, yet this wavelength region (350-2500 nm) is widely used for remote sensing. This study presents detailed analyses of the 350-2500 nm reflectance spectra of 47 fine-grained powders of different high-purity solid-state PAHs. Spectral properties of PAHs change with variations in the number and connectivity of linked aromatic rings and the presence and type of side-groups and heterocycles. PAH spectra are characterized by three strong features near ∼880 nm, ∼1145 nm, and ∼1687 nm due to overtones of νCH fundamental stretching vibrations. Some PAHs are amenable to remote detection due to the presence of diagnostic spectral features, including: Nsbnd H stretching overtones at 1490-1515 nm in NH- and NH2-bearing PAHs, aliphatic or saturated bond Csbnd H overtone vibrations at ∼1180-1280 nm and ∼1700-1860 nm; a broad asymmetric feature between ∼1450 nm and ∼1900 nm due to Osbnd H stretching overtones in aromatic alcohols, Csbnd H and Cdbnd O combinations near ∼2000-2010 nm and ∼2060-2270 nm in acetyl and carboxyl-bearing PAHs. Other substituents such as sulphonyl, thioether ether and carboxyl heterocycles, or cyano, nitrate, and aromatic side groups, do not produce well-resolved diagnostic spectral features but do cause shifts in the positions of the aromatic Csbnd H vibrational overtone features. Fluorescence is commonly suppressed by the presence of heterocycles, side-groups and in many non-alternant PAHs

  9. Cardiac Autonomic Dysfunction from Occupational Exposure to Polycyclic Aromatic Hydrocarbons

    PubMed Central

    Lee, Mi-Sun; Magari, Shannon; Christiani, David C.

    2013-01-01

    Objectives Polycyclic aromatic hydrocarbons (PAHs) exposures have been associated with cardiopulmonary mortality and cardiovascular events. This study investigated the association between a biological marker of PAHs exposure, assessed by urinary 1-hydroxypyrene (1-OHP), and heart rate variability (HRV) in an occupational cohort of boilermakers. Methods Continuous 24-hour monitoring of the ambulatory electrocardiogram (ECG) and pre and post shift urinary 1-OHP were repeated over extended periods of the work week. Mixed effects models were fit for the 5-minute standard deviation of normal-to-normal intervals (SDNN) in relation to urinary 1-OHP levels pre and post workshift on the day they wore the monitor, controlling for potential confounders. Results We found a significant decrease in 5-min SDNN during work of −13.6% (95% confidence interval, −17.2% to −9.8%) for every standard deviation (0.53 microgram/gram [μg/g] creatinine) increase in the next-morning pre-shift 1-OHP levels. The magnitude of reduction in 5-min SDNN were largest during the late night period after work and increased with every standard deviation (0.46 μg/g creatinine) increase in post-shift 1-OHP levels. Conclusion This is the first report providing evidence that occupational exposure to PAHs is associated with altered cardiac autonomic function. Acute exposure to PAHs may be an important predictor of cardiovascular disease risk in the work environment. PMID:21172795

  10. Polycyclic aromatic hydrocarbons and metals in snow along a highway.

    PubMed

    Reinosdotter, K; Viklander, M; Malmqvist, P A

    2006-01-01

    Snow quality and its variations due to distance from the road were studied. Also, how the snow quality changes over time during the melting period was discussed. Snow samples were collected at three occasions during the winter of 2004. The samples were taken along a highway in the Luleå region, Sweden, with an average daily traffic load of 9200 vehicles. Snow samples were taken perpendicular to the road and at different distances. The snow samples were analysed for metals and polycyclic aromatic hydrocarbons (PAH). Also, weather parameters such as temperature, precipitation, and wind speed and wind direction were measured. The highest total metal and PAH concentrations were found at the sample site closest to the road and at the end of the season. Before the melting period started, 42-57% of the total amount of metals and PAH were found in the first 1 m of the snow pack. This information could be valuable when one is discussing how to achieve sustainable snow-handling management.

  11. Polycyclic Aromatic Hydrocarbons as Star Formation Rate Indicators

    NASA Astrophysics Data System (ADS)

    Calzetti, D.

    2011-03-01

    As images and spectra from ISO and Spitzer have provided increasingly higher-fidelity representations of the mid-infrared (MIR) and Polycyclic Aromatic Hydrocarbon (PAH) emission from galaxies and galactic and extra-galactic regions, more systematic efforts have been devoted to establishing whether the emission in this wavelength region can be used as a reliable star formation rate indicator. This has also been in response to the extensive surveys of distant galaxies that have accumulated during the cold phase of the Spitzer Space Telescope. Results so far have been somewhat contradictory, reflecting the complex nature of the PAHs and of the mid-infrared-emitting dust in general. The two main problems faced when attempting to define a star formation rate indicator based on the mid-infrared emission from galaxies and star-forming regions are: (1) the strong dependence of the PAH emission on metallicity; (2) the heating of the PAH dust by evolved stellar populations unrelated to the current star formation. I review the status of the field, with a specific focus on these two problems, and will try to quantify the impact of each on calibrations of the mid-infrared emission as a star formation rate indicator.

  12. Secondary organic aerosol from polycyclic aromatic hydrocarbons in Southeast Texas

    NASA Astrophysics Data System (ADS)

    Zhang, Hongliang; Ying, Qi

    2012-08-01

    Recent chamber studies show that low-volatility gas phase precursors such as polycyclic aromatic hydrocarbons (PAHs) can be a significant source of secondary organic aerosol (SOA). In this work, formation of SOA from the photo-oxidation products of PAHs is added to the SOA modeling framework of the Community Multiscale Air Quality (CMAQ) model to determine the regional distribution of SOA products from PAHs (PAH-SOA) and the contributions from sources in Southeast Texas during the Texas Air Quality Study 2006 (TexAQS 2006). Results show that PAHs released from anthropogenic sources can produce SOA mass as much as 10% of that from the traditional light aromatics or approximately 4% of total anthropogenic SOA. In areas under the influence of wildfire emissions, the amount of PAH-SOA can be as much as 50% of the SOA from light aromatics. A source-oriented modeling framework is adopted to determine the major sources of PAH-SOA by tracking the emitted PAHs and their oxidation products in the gas and aerosol phases from different sources separately. Among the eight sources (vehicles, solvent utilization, residential wood, industries, natural gas combustion, coal combustion, wildfire and other sources) that are tracked in the model, wildfire, vehicles, solvent and industries are the major sources of PAH-SOA. Coal and natural gas combustion appear to be less important in terms of their contributions to PAH-SOA.

  13. Sources of polycyclic aromatic hydrocarbons to the Hudson River Airshed

    NASA Astrophysics Data System (ADS)

    Lee, Jong Hoon; Gigliotti, Cari L.; Offenberg, John H.; Eisenreich, Steven J.; Turpin, Barbara J.

    2004-11-01

    Sources of polycyclic aromatic hydrocarbons (PAHs) to the Hudson River Estuary Airshed were investigated using positive matrix factorization (PMF). A three-city dataset was used to obtain common factor profiles. The contributions of each factor on each sampling day and site were then determined, and a sensitivity analysis was conducted. A stable eight-factor solution was identified. PMF was able to identify a factor associated with air-surface exchange. This factor contains low-molecular weight PAHs and was a dominant contributor to the measured PAHs concentrations. Factors linked to motor vehicle use (diesel and gasoline vehicle emissions and evaporative/uncombusted petroleum) and natural gas combustion were also major contributors. Motor vehicle combustion and oil combustion factors were the predominant contributors to particle-phase PAHs, while natural gas combustion, air-surface exchange, and evaporative/uncombusted petroleum factors made substantial contributions to gas-phase PAH concentrations. In contrast to fine particulate matter (PM2.5), which is dominated by regional transport, spatial variations in PAH concentrations suggest that PAH concentrations in the Hudson River Estuary Airshed are dominated by sources within the New York-New Jersey urban-industrial complex.

  14. Distribution of polycyclic aromatic hydrocarbons in coke plant wastewater.

    PubMed

    Burmistrz, Piotr; Burmistrz, Michał

    2013-01-01

    The subject of examinations presented in this paper is the distribution of polycyclic aromatic hydrocarbons (PAHs) between solid and liquid phases in samples of raw wastewater and wastewater after treatment. The content of 16 PAHs according to the US EPA was determined in the samples of coke plant wastewater from the Zdzieszowice Coke Plant, Poland. The samples contained raw wastewater, wastewater after physico-chemical treatment as well as after biological treatment. The ΣPHA16 content varied between 255.050 μg L(-1) and 311.907 μg L(-1) in raw wastewater and between 0.940 and 4.465 μg L(-1) in wastewater after full treatment. Investigation of the distribution of PAHs showed that 71-84% of these compounds is adsorbed on the surface of suspended solids and 16-29% is dissolved in water. Distribution of individual PAHs and ΣPHA16 between solid phase and liquid phase was described with the use of statistically significant, linear equations. The calculated values of the partitioning coefficient Kp changed from 0.99 to 7.90 for naphthalene in samples containing mineral-organic suspension and acenaphthylene in samples with biological activated sludge, respectively.

  15. Polycyclic Aromatic Hydrocarbon Ionization Energy Lowering in Water Ices

    NASA Technical Reports Server (NTRS)

    Gudipati, Murthy S.; Allamandola, Louis J.

    2004-01-01

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

  16. Investigation of polycyclic aromatic hydrocarbons from coal gasification.

    PubMed

    Zhou, Hong-cang; Jin, Bao-sheng; Zhong, Zhao-ping; Huang, Ya-ji; Xiao, Rui; Li, Da-ji

    2005-01-01

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

  17. Tailoring Colors by O Annulation of Polycyclic Aromatic Hydrocarbons

    PubMed Central

    Miletić, Tanja; Fermi, Andrea; Orfanos, Ioannis; Avramopoulos, Aggelos; De Leo, Federica; Demitri, Nicola; Bergamini, Giacomo; Ceroni, Paola; Papadopoulos, Manthos G.; Couris, Stelios

    2017-01-01

    Abstract The synthesis of O‐doped polyaromatic hydro‐ carbons in which two polycyclic aromatic hydrocarbon sub units are bridged through one or two O atoms has been achieved. This includes high‐yield ring‐closure key steps that, depending on the reaction conditions, result in the formation of furanyl or pyranopyranyl linkages through intramolecular C−O bond formation. Comprehensive photophysical measurements in solution showed that these compounds have exceptionally high emission yields and tunable absorption properties throughout the UV/Vis spectral region. Electrochemical investigations showed that in all cases O annulation increases the electron‐donor capabilities by raising the HOMO energy level, whereas the LUMO energy level is less affected. Moreover, third‐order nonlinear optical (NLO) measurements on solutions or thin films containing the dyes showed very good values of the second hyperpolarizability. Importantly, poly(methyl methacrylate) films containing the pyranopyranyl derivatives exhibited weak linear absorption and NLO absorption compared to the nonlinearity and NLO refraction, respectively, and thus revealed them to be exceptional organic materials for photonic devices. PMID:27897357

  18. Xenoestrogenic gene expression: structural features of active polycyclic aromatic hydrocarbons.

    PubMed

    Schultz, T Wayne; Sinks, Glendon D

    2002-04-01

    Estrogenicity was assessed using the Saccharomyces cerevisiae-based Lac-Z reporter assay and was reported as the logarithm of the inverse of the 50% molar beta-galactosidase activity (log[EC50(-1)]). In an effort to quantify the relationship between molecular structure of polycyclic aromatic hydrocarbons (PAHs) and estrogenic gene expression, a series of PAHs were evaluated. With noted exceptions, the results of these studies indicate that the initial two-dimensional structural warning for estrogenicity, the superpositioning of a hydroxylated aromatic system on the phenolic A-ring of 17-beta-estradiol, can be extended to the PAHs. This two-dimensional-alignment criterion correctly identified estrogenicity of 22 of the 29 PAHs evaluated. Moreover, the estrogenic potency of these compounds was directly related to the size of the hydrophobic backbone. The seven compounds classified incorrectly by this structural feature were either dihydroxylated naphthalenes or aromatic nitrogen-heterocyclic compounds; all such compounds were false positives. Results with dihydroxylated naphthalenes reveal derivatives that were nonestrogenic when superimposed on the phenolic A-ring of 17-beta-estradiol had the second hydroxyl group in the position of the C-ring or were catechol-like in structure. Structural alerts for nitrogen-heterocyclic compounds must take into account the position of the hydroxyl group and the in-ring nitrogen atom; compounds with the hydroxyl group and nitrogen atom involved with the same ring were observed to be nonactive.

  19. A critical review of polycyclic aromatic hydrocarbon phototoxicity models.

    PubMed

    Marzooghi, Solmaz; Di Toro, Dominic M

    2016-12-24

    Polycyclic aromatic hydrocarbons (PAHs) are known to exhibit photo-induced toxicity. Hundreds to thousands of PAH parent and substituted compounds are found in the environment, and developing a predictive model applicable to a wide variety of PAHs and organisms is a necessary precursor to environmental risk assessments. There has been evolutionary progress in phototoxicity modeling since 1977. In the present study, a comprehensive review of the models developed to predict phototoxicity of PAHs is presented. The contributions of each of the models to the state of the art are discussed. The models are compared in terms of their scope of applicability to different organisms, PAHs, endpoints (median lethal time and median lethal concentration), and light conditions. The current state of the science that accounts for the key elements of phototoxicity modeling, including the differences in species sensitivity, the partitioning of PAHs into the target lipid of the organisms, and light absorption by the chemicals, as well as light exposure time and conditions, is discussed. In addition, the remaining issues that need to be addressed are explored: the effect of time-varying exposures to light and PAH concentrations, and the lack of a mechanistic understanding that can explain the failure of the Bunsen-Roscoe law of reciprocity. Environ Toxicol Chem 2016;9999:1-11. © 2016 SETAC.

  20. Polycyclic aromatic hydrocarbon ions and the diffuse interstellar bands

    NASA Technical Reports Server (NTRS)

    Salama, F.; Allamandola, L. J.

    1995-01-01

    Neutral naphthalene (C10H8), phenanthrene (C14H10), and pyrene (C16H10) absorb strongly in the ultraviolet and may contribute to the extinction curve. High abundances are required to produce detectable structures. The cations of these Polycyclic Aromatic Hydrocarbons (PAHs) absorb in the visible. C10H8(+) has 12 discrete absorption bands which fall between 6800 and 5000 A. The strongest band at 6741 A falls close to the weak 6742 A diffuse interstellar band (DIB). Five other weaker bands also match DIBs. The possibility that C10H8(+) is responsible for some of the DIBs can be tested by searching for new DIBS at 6520, 6151, and 5965 A, other moderately strong naphthalene cation band positions. If C10H8(+) is indeed responsible for the 6742 A feature, it accounts for 0.3% of the cosmic carbon. The spectrum of C16H10(+) is dominated by a strong band at 4435 A in an Ar matrix and 4395 A in a Ne matrix, a position which falls very close to the strongest DIB, that at 4430 A. If C16H10(+), or a closely related pyrene-like ion is indeed responsible for the 4430 A feature, it accounts for 0.2% of the cosmic carbon. We also report an intense, very broad UV-to-visible continuum which is associated with both ions and could explain how PAHs convert interstellar UV and visible radiation into IR.

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

    PubMed

    Becker, L; Bunch, T E

    1997-07-01

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

  2. Vibrational spectroscopic study of vinyl substituted polycyclic aromatic hydrocarbons.

    PubMed

    Maurya, Anju; Rastogi, Shantanu

    2015-12-05

    The mid infrared emission features observed in various astrophysical sources are attributed to polycyclic aromatic hydrocarbon (PAH) molecules. The models of emission spectra from a collection of PAHs show uncertainty in matching the 6.2 μm feature. This indicates the need to consider a larger variety of PAHs and PAH derivatives. Chemical pathways towards formation of PAHs in the astrophysical environments involve vinyl substituted PAHs as intermediate products. Vibrational spectroscopic study of vinyl-PAHs is reported in the present work. The vinyl group is substituted at similar positions in eight different PAHs. The obtained optimized structures show that vinyl substitution at 2 position in acenes gives planar geometry, while all other vinyl-PAHs are non-planar. Infrared spectra is simulated for neutrals as well as for cations. The results are compared with the spectra of corresponding plain PAHs and analyzed for possible match with astrophysical observations. New features, due to vinyl group in the composite spectra, identified at 6.64, 6.92, 7.27, 8.77 and 10.35 μm fall close to some sub features of the observed emission spectra. The paper provides data that may be used in the emission models particularly along proto planetary nebulae type cool objects.

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

    SciTech Connect

    Ping Sun; Panuwat Taerakul; Linda K. Weavers; Harold W. Walker

    2005-10-01

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

  4. Particle-bound polycyclic aromatic hydrocarbon concentrations in transportation microenvironments

    NASA Astrophysics Data System (ADS)

    Houston, Douglas; Wu, Jun; Yang, Dongwoo; Jaimes, Guillermo

    2013-06-01

    This study is one of the first case studies to characterize the exposure of urban residents to traffic-related air pollution across locations and transportation microenvironments during everyday activities. Twenty-four adult residents of Boyle Heights, a neighborhood near downtown Los Angeles, carried a portable air pollution monitor and a Global Positioning Systems (GPS) tracking device for a total of 96 days. We found significant spatial and temporal variation in the particle-bound polycyclic aromatic hydrocarbon (pPAH) concentrations in transportation microenvironments. Average pPAH concentrations were higher while walking outdoors (190 ng m-3) compared to traveling in private passenger vehicles (138-155 ng m-3) or traveling in public transportation (61-124 ng m-3). Although travel comprised 5% of participant days, it was associated with 27% of overall daily pPAH exposure. Regression models explained 40-55% of the variation in daily average pPAH concentrations, and 40-44% of the variation in 1-min interval concentrations. Important factors included time spent traveling, travel speed, meteorological and nearby land use factors, time of day, and proximity to roadways. Although future research is needed to develop stronger predictive models, our study demonstrates portable tracking devices can provide a more complete, diurnal characterization of air pollution exposures for urban populations.

  5. Polycyclic aromatic hydrocarbons and pesticides in milk powder.

    PubMed

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

    2016-05-01

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

  6. Fugacity analysis of polycyclic aromatic hydrocarbons between microplastics and seawater

    NASA Astrophysics Data System (ADS)

    Lee, Hwang; Chang, Sein; Kim, Seung-Kyu; Kwon, Jung-Hwan

    2017-03-01

    Recently, the accumulation of plastic debris in the marine environment has become a great concern worldwide. Although plastics are biologically and chemically inert, plastic debris has been suspected of causing adverse effects on ecosystems due to the increase in reactivity by size reduction and/or micropollutants associated with plastics. Because of the high sorption capacity of microplastics toward organic micropollutants, it is suspected that microplastics may play roles in the distribution and fate of micropollutants. In order to quantitatively evaluate the "net flow" of environmental contaminants in water-plastic-organism systems, a fugacity analysis was conducted using concentrations of polycyclic aromatic hydrocarbons (PAHs) in open oceans and in polyethylene as a representative material of plastic debris. Ratio of fugacity in polyethylene to that in seawater showed a decreasing trend with increasing partition coefficient between polyethylene and seawater (KPE/sw). This indicates that phase equilibrium between polyethylene and seawater is not attained for higher molecular weight PAHs. Disequilibrium of high molecular weight PAHs suggests that transfer from seawater to plastic debris is thermodynamically driven and the role of plastic debris as a vector to transfer them to living organisms would be minimal. However, additives may slowly migrate from plastics into the environment causing potentially serious effects on ecosystems.

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

    NASA Astrophysics Data System (ADS)

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

    2014-10-01

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

  8. Atmospheric transport and outflow of polycyclic aromatic hydrocarbons from China

    SciTech Connect

    Chang Lang; Shu Tao; Wenxin Liu; Yanxu Zhang; Staci Simonich

    2008-07-15

    A potential receptor influence function (PRIF) model, based on air mass forward trajectory calculations, was applied to simulate the atmospheric transport and outflow of polycyclic aromatic hydrocarbons (PAHs) emitted from China. With a 10 day atmospheric transport time, most neighboring countries and regions, as well as remote regions, were influenced by PAH emissions from China. Of the total annual PAH emission of 114 Gg, 92.7% remained within the boundary of mainland China. The geographic distribution of PRIFs within China was similar to the geographic distribution of the source regions, with high values in the North China Plain, Sichuan Basin, Shanxi, and Guizhou province. The Tarim basin and Sichuan basin had unfavorable meteorological conditions for PAH outflow. Of the PAH outflow from China (8092 tons or 7.1% of the total annual PAH emission), approximately 69.9% (5655 tons) reached no further than the offshore environment of mainland China and the South China Sea. Approximate 227, 71, 746, and 131 tons PAHs reached North Korea, South Korea, Russia-Mongolia region, and Japan, respectively, 2-4 days after the emission. Only 1.4 tons PAHs reached North America after more than 9 days. Interannual variation in the eastward PAH outflow was positively correlated to cold episodes of El Nino/Southern Oscillation. However, trans-Pacific atmospheric transport of PAHs from China was correlated to Pacific North America index (PNA) which is associated with the strength and position of westerly winds. 38 refs., 4 figs.

  9. Risk assessment of polycyclic aromatic hydrocarbons in aquatic ecosystems.

    PubMed

    Wu, Bing; Zhang, Rui; Cheng, Shu-Pei; Ford, Timothy; Li, Ai-Min; Zhang, Xu-Xiang

    2011-07-01

    A probability risk assessment of anthracene, benzo(a)pyrene, chrysene, fluorene, phenanthrene and pyrene was carried out to examine the ecological risk of these six polycyclic aromatic hydrocarbons (PAHs) in aquatic ecosystems in China. The literature on PAH concentrations in surface water in China was collected to evaluate the environmental exposure concentrations (EEC). The 10th percentile of predicted no observed effect concentration (PNEC(10%)) of PAHs, calculated according to the data from the USEPA AQUIRE database and regulatory reviews, was applied as the toxicity assessment endpoint. The ratio of EEC and PNEC(10%), expressed as a risk quotient (RQ), was used to characterize the risk value. Bootstrapping method and Monte Carlo simulation were utilized to calculate the distribution of EEC, PNEC(10%), RQ and associated uncertainties. Risk assessment showed that reliable maximum RQs of anthracene, benzo(a)pyrene, chrysene, fluorene and phenanthrene were in the range of 0.064-0.755, lower than the acceptable value of 1. However, the reliable maximum RQ of pyrene was 1.39, indicating its potential ecological risk. Notwithstanding the uncertainty, these results suggest that the aquatic ecosystems with high PAH concentrations might pose potential ecological risks, and concerted efforts are required to ensure that surface water is protected.

  10. Remediation of Polycyclic Aromatic Hydrocarbons in Soil Using Cosolvent Flushing

    NASA Astrophysics Data System (ADS)

    Birak, P. S.; Hauswirth, S.; Miller, C. T.

    2010-12-01

    The ability of cosolvents to increase the solubility of hydrophobic organic contaminants has been well documented in the literature; however, few studies have examined its effectiveness with respect to field contaminated media. In this work, we examine the use of methanol flushing as a possible in-situ remediation technology using an aged, tar-contaminated field soil from a former manufactured gas plant containing polycyclic aromatic hydrocarbons (PAHs). For 15 PAHs, batch experiments were used to determine the change in the equilibrium partitioning coefficient with cosolvent fraction based on a log-linear cosolvency model. Column experiments were conducted to examine the removal of PAHs using methanol solutions as a function of pore volumes flushed. Experiments were conducted in a 25-cm long glass column. Effluent concentrations were determined for PAHs. Methanol concentrations in effluent samples were also determined. A numerical model with coupled flow and transport equations was used to predict effluent concentrations of methanol and PAHs. During cosolvent flushing with 95% methanol solutions, approximately 80% of the total PAH mass was removed in the first four pore volumes. The remaining mass in the column appeared to be mass transfer limited, particularly for the low molecular weight PAHs.

  11. Large Abundances of Polycyclic Aromatic Hydrocarbons in Titan's Upper Atmosphere

    NASA Technical Reports Server (NTRS)

    Lopez-Puertas, M.; Dinelli, B. M.; Adriani, A.; Funke, B.; Garcia-Comas, M.; Moriconi, M. L.; D'Aversa, E.; Boersma, C.; Allamandola, L. J.

    2013-01-01

    In this paper, we analyze the strong unidentified emission near 3.28 micron in Titan's upper daytime atmosphere recently discovered by Dinelli et al.We have studied it by using the NASA Ames PAH IR Spectroscopic Database. The polycyclic aromatic hydrocarbons (PAHs), after absorbing UV solar radiation, are able to emit strongly near 3.3 micron. By using current models for the redistribution of the absorbed UV energy, we have explained the observed spectral feature and have derived the vertical distribution of PAH abundances in Titan's upper atmosphere. PAHs have been found to be present in large concentrations, about (2-3) × 10(exp 4) particles / cubic cm. The identified PAHs have 9-96 carbons, with a concentration-weighted average of 34 carbons. The mean mass is approx 430 u; the mean area is about 0.53 sq. nm; they are formed by 10-11 rings on average, and about one-third of them contain nitrogen atoms. Recently, benzene together with light aromatic species as well as small concentrations of heavy positive and negative ions have been detected in Titan's upper atmosphere. We suggest that the large concentrations of PAHs found here are the neutral counterpart of those positive and negative ions, which hence supports the theory that the origin of Titan main haze layer is located in the upper atmosphere.

  12. Infrared Spectroscopy of Matrix-Isolated Polycyclic Aromatic Hydrocarbon Cations

    NASA Technical Reports Server (NTRS)

    Hudgins, D. M.; Allamandola, L. J.

    1995-01-01

    Gaseous, ionized polycyclic aromatic hydrocarbons (PAHs) are thought to be responsible for a very common family of interstellar infrared emission bands. Here the near- and mid-infrared spectra of the cations of the five most thermodynamically favored PAHs up to coronene: phenanthrene, pyrene, benzo(e)pyrene, benzo-(ghi)perylene, and coronene, are presented to test this hypothesis. For those molecules that have been studied previously (pyrene, pyrene-d(sub 10), and coronene), band positions and relative intensities are in agreement. In all of these cases we report additional features. Absolute integrated absorbance values are given for the phenanthrene, perdeuteriophenanthrene, pyrene, benzo(ghi]perylene, and coronene cations. With the exception of coronene, the cation bands corresponding to the CC modes are typically 2-5 times more intense than those of the CH out-of-plane bending vibrations. For the cations, the CC stretching and CH in-plane bending modes give rise to bands that are an order of magnitude stronger than those of the neutral species, and the CH out-of-plane bends produce bands that are 5-20 times weaker than those of the neutral species. This behavior is similar to that found in most other PAH cations studied to date. The astronomical implications of these PAH cation spectra are also discussed.

  13. Determinants of polycyclic aromatic hydrocarbon levels in house dust.

    PubMed

    Whitehead, Todd; Metayer, Catherine; Gunier, Robert B; Ward, Mary H; Nishioka, Marcia G; Buffler, Patricia; Rappaport, Stephen M

    2011-01-01

    Estimation of human exposures to polycyclic aromatic hydrocarbons (PAHs) is often desired for the epidemiological studies of cancer. One way to obtain information about indoor levels of PAHs is to measure these chemicals in house dust. In this study, we evaluated the predictive value of self-reported and geographic data for estimating measured levels of nine PAHs in house dust from 583 households in the Northern California Childhood Leukemia Study (NCCLS). Using multivariable linear regression models, we evaluated the effects on house-dust PAH concentrations from the following covariates: residential heating sources, smoking habits, house characteristics, and outdoor emission sources. House dust was collected from 2001 to 2007, using both high-volume surface samplers and household vacuum cleaners, and was analyzed for nine PAHs using gas chromatography-mass spectrometry. All nine PAHs were detected in more than 93% of dust samples, with median concentrations ranging from 14 to 94 ng/g dust. Statistically significant effects on PAH concentrations in house dust were found for gas heating, outdoor PAH concentrations, and residence age. Yet, the optimal regression model only explained 15% of the variation in PAH levels in house dust. As self-reported data and outdoor PAH sources were only marginally predictive of observed PAH levels, we recommend that PAH concentrations be measured directly in dust samples for use in epidemiological studies.

  14. Stochastic atomistic simulation of polycyclic aromatic hydrocarbon growth in combustion.

    PubMed

    Lai, Jason Y W; Elvati, Paolo; Violi, Angela

    2014-05-07

    Nanoparticles formed in gas phase environments, such as combustion, have an important impact on society both as engineering components and hazardous pollutants. A new software package, the Stochastic Nanoparticle Simulator (SNAPS) was developed, applying a stochastic chemical kinetics methodology, to computationally investigate the growth of nanoparticle precursors through trajectories of chemical reactions. SNAPS was applied to characterize the growth of polycyclic aromatic hydrocarbons (PAHs), important precursors of carbonaceous nanoparticles and soot, in a premixed laminar benzene flame, using a concurrently developed PAH growth chemical reaction mechanism, as well as an existing benzene oxidation mechanism. Simulations of PAH ensembles successfully predicted existing experimentally measured data and provided novel insight into chemical composition and reaction pathways. The most commonly observed PAH isomers in simulations showed the importance of 5-membered rings, which contrasts with traditionally assumed compositions involving primarily pericondensed 6-membered rings. In addition, the chemical growth of PAHs involved complex sequences of highly reversible reactions, rather than relatively direct routes of additions and ring closures. Furthermore, the most common reactions involved 5-membered rings, suggesting their importance to PAH growth. The framework developed in this work will facilitate future investigation of particle inception and soot formation and will benefit engineering of novel combustion technologies to mitigate harmful emissions.

  15. An Evaluation of Polycyclic Aromatic Hydrocarbon Uptake into Polyethylene Samplers

    NASA Astrophysics Data System (ADS)

    Martynowych, D. J.; McDonough, C.; Lohmann, R.

    2013-12-01

    Polyethylene passive samplers (PEs) are simple reliable tools that have been widely used in the detection of hydrophobic organic compounds. Thick (>200μm or greater) PEs have important applications to specific sampling scenarios including biological assays, deployment on ships and aircraft (towing) and long term sampling, however little is known about their uptake kinetics. This study aimed to develop an accurate understanding of the uptake kinetics of these thick PEs. PE passive samplers of equal surface area, but differing thicknesses were co-deployed in the surface water and air of lower Narragansett Bay in 2013 to characterize differences in their uptake of polycyclic aromatic hydrocarbons (PAHs). PE samplers of approximately 50, 800, and 1600μm thicknesses were analyzed for 38 parent and alkylated PAHs, with replicate sampler reproducibility mostly within 25%. A number of smaller PAHs (typically those with a molecular weight less than 180) analyzed over a 4 week deployment equilibrated, while the larger molecules remained in the linear or curve linear uptake stages. Results from a second, 24 week deployment of 800μm and 1600μm samplers in surface waters suggest that all 38 compounds studied remained in the linear uptake stage. The PE-weight normalized concentration ratio of 1600μm to 800μm sampler fell below 1 for all analytes, implying equilibrium had not been established.

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

    NASA Technical Reports Server (NTRS)

    Becker, L.; Bunch, T. E.

    1997-01-01

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

  17. Dusty Winds: Extraplanar Polycyclic Aromatic Hydrocarbon Features of Nearby Galaxies

    NASA Astrophysics Data System (ADS)

    McCormick, Alexander; Veilleux, Sylvain; Rupke, David S. N.

    2013-09-01

    Recent observations have shown the presence of dust and molecular material in galactic winds, but relatively little is known about the distribution of these outflow components. To shed some light on this issue, we have used IRAC images from the Spitzer Space Telescope archive to investigate polycyclic aromatic hydrocarbon (PAH) emission from a sample of 16 local galaxies with known winds. Our focus on nearby sources (median distance 8.6 Mpc) has revealed detailed PAH structure in the winds and allowed us to measure extraplanar PAH emission. We have identified extraplanar PAH features on scales of ~0.8-6.0 kpc. We find a nearly linear correlation between the amount of extraplanar PAH emission and the total infrared flux, a proxy for star formation activity in the disk. Our results also indicate a correlation between the height of extraplanar PAH emission and star formation rate surface density, which supports the idea of a surface density threshold on the energy or momentum injection rate for producing detectable extraplanar wind material.

  18. Formation History of Polycyclic Aromatic Hydrocarbons in Galaxies

    NASA Astrophysics Data System (ADS)

    Seok, J. Y.; Hirashita, H.; Asano, R.

    Polycyclic aromatic hydrocarbons (PAHs) are one of the major dust components in the interstellar medium (ISM). We present our model calculations for the PAH abundance in the ISM on a galaxy-evolution timescale. We consider shattering of carbonaceous dust grains as the formation mechanism of PAHs while the PAH abundance is reduced by coagulation onto dust grains, destruction by supernova shocks, and injection into star formation. We implement these processes in an one-zone chemical evolution model to obtain the evolution of the PAH abundance in a galaxy. We find that PAH formation becomes accelerated at a certain metallicity at which shattering becomes efficient. For PAH destruction, while supernova shock is a primary mechanism in the metal-poor environment, coagulation is dominant in the metal-rich environment. We compare the calculated PAH abundances with the observed abundances in galaxies with a wide metallicity range. Our models reproduce both the low PAH abundance in low metallicity galaxies and the metallicity-dependence of the PAH abundance in high-metallicity galaxies. We conclude that the observational trend can be explained by shattering of carbonaceous grains being the source of PAHs in the ISM.

  19. Fugacity analysis of polycyclic aromatic hydrocarbons between microplastics and seawater

    NASA Astrophysics Data System (ADS)

    Lee, Hwang; Chang, Sein; Kim, Seung-Kyu; Kwon, Jung-Hwan

    2017-01-01

    Recently, the accumulation of plastic debris in the marine environment has become a great concern worldwide. Although plastics are biologically and chemically inert, plastic debris has been suspected of causing adverse effects on ecosystems due to the increase in reactivity by size reduction and/or micropollutants associated with plastics. Because of the high sorption capacity of microplastics toward organic micropollutants, it is suspected that microplastics may play roles in the distribution and fate of micropollutants. In order to quantitatively evaluate the "net flow" of environmental contaminants in water-plastic-organism systems, a fugacity analysis was conducted using concentrations of polycyclic aromatic hydrocarbons (PAHs) in open oceans and in polyethylene as a representative material of plastic debris. Ratio of fugacity in polyethylene to that in seawater showed a decreasing trend with increasing partition coefficient between polyethylene and seawater (KPE/sw). This indicates that phase equilibrium between polyethylene and seawater is not attained for higher molecular weight PAHs. Disequilibrium of high molecular weight PAHs suggests that transfer from seawater to plastic debris is thermodynamically driven and the role of plastic debris as a vector to transfer them to living organisms would be minimal. However, additives may slowly migrate from plastics into the environment causing potentially serious effects on ecosystems.

  20. Bioaccessibility of polycyclic aromatic hydrocarbons: relevance to toxicity and carcinogenesis

    PubMed Central

    Harris, Kelly L; Banks, Leah D; Mantey, Jane A; Huderson, Ashley C; Ramesh, Aramandla

    2014-01-01

    Introduction Bioaccessibility is a growing area of research in the field of risk assessment. As polycyclic aromatic hydrocarbons (PAHs) are ubiquitous environmental pollutants, they are the toxicants of focus to establish cancer risks in humans. Orally ingested PAHs also cause toxicity and even affect the pharmacokinetic behavior of some therapeutic agents. Toward this end, bioaccessibility is being used as a tool to assess the risk of PAHs via dietary exposures. Areas covered This review covers some in vitro bioaccessibility models for PAHs that have been used for the past one-and-a-half decade. This review also considers the factors that influence bioaccessibility and debates the merits and limitations of using a bioaccessibility concept for estimating risk from ingestion of PAH-contaminated soil and food. Finally, the authors discuss the implications of bioaccessibility for PAH-induced toxicity and cancers in the context of risk assessment. Expert opinion So far, much of the focus on PAH bioaccessibility is centered on soil as a preferential matrix. However, ingestion of PAHs through diet far exceeds the amount accidentally ingested through soil. Therefore, bioaccessibility could be exploited as a tool to assess the relative risk of various dietary ingredients tainted with PAHs. While bioaccessibility is a promising approach for assessing PAH risk arising from various types of contaminated soils, none of the models proposed appears to be valid. Bioaccessibility values, derived from in vitro studies, still require validation from in vivo studies. PMID:23898780

  1. Polycyclic Aromatic Hydrocarbons in drinking water of Tehran, Iran

    PubMed Central

    2013-01-01

    Distribution and seasonal variation of sixteen priority polycyclic aromatic hydrocarbons (PAHs) were investigated in the drinking water of Tehran, the capital of Iran. Detected single and total PAHs concentrations were in the range of 2.01-38.96 and 32.45-733.10 ng/L, respectively, which were quite high compared to the values recorded in other areas of the world. The average occurrence of PAHs with high molecular weights was 79.55%; for example, chrysene occurred in 60.6% of the samples, with a maximum concentration of 438.96 ng/L. In addition, mean carcinogen to non-carcinogen PAHs ratio was 63.84. Although the concentration of benzo[a]pyrene, as an indicator of water pollution to PAHs, was lower than the guideline value proposed by World Health Organization (WHO) as well as that of Iranian National Drinking Water Standards for all of the samples, the obtained results indicated that carcinogen PAHs present in the drinking water of Tehran can cause threats to human health. PMID:24499505

  2. Plant bioindicators for polycyclic aromatic hydrocarbon toxicity in aquatic microcosms

    SciTech Connect

    Gensemer, R.W.; Solomon, K.R.; Day, K.E.; Hodson, P.V.; Servos, M.R.; Greenberg, B.M.

    1994-12-31

    Plant bioindicators are being developed to assess the effects of polycyclic aromatic hydrocarbons (PAHs) in experimental aquatic ecosystems. The approach is to develop and test biomarker assays that are specifically predictive of ecological events at the population and/or community levels of organization in artificial aquatic microcosms. PAH mixtures were introduced into a series of aquatic microcosms using the wood preservative creosote as a PAH source. The authors applied creosote at five dosage levels designed to simulate conductions observed at highly contaminated sites. The growth and biomass of phytoplankton, periphyton, and macrophytes were then measured throughout the growing season, and compared to one or more biomarker assays used to detect PAH contamination. Preliminary results using fluorescence induction on aquatic macrophytes suggest that PAHs can significantly inhibit photosynthesis at even modest concentrations 1--4 hours after exposure. This assay thus is not only a sensitive indicator of PAH exposure, but may also describe mechanisms of PAH toxicity that ultimately reduce biomass or population growth for aquatic plants in these microcosms.

  3. Molecular Spectroscopy in Astrophysics: The Case of Polycyclic Aromatic Hydrocarbons

    NASA Technical Reports Server (NTRS)

    Salama, Farid; DeVincent, Donald L. (Technical Monitor)

    2000-01-01

    The role of molecular spectroscopy in astrophysics and astrochemistry is discussed in the context of the study of large, complex, carbon-bearing molecules, namely, Polycyclic Aromatic Hydrocarbons or PAHs. These molecular species are now thought to be widespread in the interstellar medium in their neutral and ionized forms. Identifying the carriers responsible for unidentified interstellar spectral bands will allow to derive important information on cosmic elemental abundances as well as information on the physical conditions (density, temperature) reigning in specific interstellar environments. These, in turn, are key elements for a correct understanding of the energetic mechanisms that govern the origin and the evolution of the interstellar medium. A multidisciplinary approach - combining astronomical observations with laboratory simulations and theoretical modeling - is required to address these complex issues. Laboratory spectra of several PAHs, isolated at low temperature in inert gas matrices or seeded in a supersonic jet expansion, are discussed here and compared to the astronomical spectra of reddened, early type, stars. The electronic spectroscopy of PAHs in the ultraviolet, visible, and near-infrared domains is reviewed and an assessment of the potential contribution of PAHs to the interstellar extinction in the ultraviolet and in the visible is discussed.

  4. Superconductivity in an Alkali Doped Polycyclic Aromatic Hydrocarbon, Picene

    NASA Astrophysics Data System (ADS)

    Tokumoto, Madoka; Shimizu, Fumihiko; Hata, Yoshiaki; Sawai, Shinya; Han, Jing; Inoue, Katsuya

    2010-03-01

    The effect of carrier doping into polycyclic aromatic hydrocarbons, including perylene and pentacene, has been extensively studied.[1] As a result of halogen or alkali metal doping, a drastic increase in electrical conductivity was observed. However, superconductivity has not been reported except the one by Sch"on et al.[2] Recently, Kubozono reported that one of them, i.e. picene (C22H14) showed superconductivity at 20 K by doping with potassium.[3] We anticipate that it will lead to surprising findings of hidden organic molecular superconductors. In this presentation, we will report on the characterization of superconducting properties of alkali doped picene. Instead of ordinary vapor phase alkali metal doping, we employ thermal decomposition of alkali azides, i.e. AN3 where A = K, Rb. We followed the doping procedure of thermal decomposition applied to fullerene C60.[4] A systematic variation of the superconducting transition temperature and fraction are studied as a function of alkali metal composition. [1] H. Akamatu, H. Inokuchi, and Y. Matsunaga, Nature 173 (1954) 168. [2] J. H. Sch"on, Ch. Kloc & B. Batlogg, Nature 406 (2000) 702; retraction, Nature 422 (2003) 93. [3] R. Mitsuhashi, Y. Kubozono et al.: private communication. [4] M. Tokumoto, et al. , J. Phys. Chem. Solids, 54 (1993) 1667.

  5. Polycyclic aromatic hydrocarbons and fatal ischemic heart disease

    SciTech Connect

    Burstyn, I.; Kromhout, H.; Partanen, T.; Svane, O.; Langard, S.; Ahrens, W.; Kauppinen, T.; Stucker, I.; Shaham, J.; Heederik, D.; Ferro, G.; Heikkila, P.; Hooiveld, M.; Johansen, C.; Randem, B.G.; Boffetta, P.

    2005-11-01

    Several toxicologic and epidemiologic studies have produced evidence that occupational exposure to polycyclic aromatic hydrocarbons (PAH) is a risk factor for ischemic heart disease (IHD). However, a clear exposure-response relation has not been demonstrated. We studied a relation between exposure to PAH and mortality from IHD (418 cases) in a cohort of 12,367 male asphalt workers from Denmark, Finland, France, Germany, Israel, The Netherlands and Norway. Exposures to benzo(a)pyrene were assessed quantitatively using measurement-driven exposure models. Exposure to coal tar was assessed in a semiquantitative manner on the basis of information supplied by company representatives. We carried out sensitivity analyses to assess potential confounding by tobacco smoking. Both cumulative and average exposure indices for benzo(a)pyrene were positively associated with mortality from IHD. The highest relative risk for fatal IHD was observed for average benzo(a)pyrene exposures of 273 ng/m{sup 3} or higher, for which the relative risk was 1.64(95% confidence interval = 1.13-2.38). Similar results were obtained for coal tar exposure. Sensitivity analysis indicated that even in a realistic scenario of confounding by smoking, we would observe approximately 20% to 40% excess risk in IHD in the highest PAH-exposure categories. Our results lend support to the hypothesis that occupational PAH exposure causes fatal IHD and demonstrate a consistent exposure-response relation for this association.

  6. Occupational exposure to Polycyclic Aromatic Hydrocarbons in wood dust

    NASA Astrophysics Data System (ADS)

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

    2009-02-01

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

  7. POLYCYCLIC AROMATIC HYDROCARBON CLUSTERS AS SOURCES OF INTERSTELLAR INFRARED EMISSION

    SciTech Connect

    Roser, J. E.; Ricca, A.

    2015-03-10

    Polycyclic aromatic hydrocarbons (or PAHs) have been the subject of astrochemical research for several decades as principal sources of the interstellar aromatic infrared emission bands. PAH clusters could possibly contribute to these emission bands, but a lack of data on their infrared properties has made this hypothesis difficult to evaluate. Here we investigate homogeneous neutral PAH clusters by measuring the mid-infrared absorption spectra of the five nonlinear PAH molecules phenanthrene, chrysene, pyrene, perylene, and benzo[ghi]perylene within solid argon ice at a fixed temperature of 5 K. We attribute observed spectral shifts in their principal absorption bands as a function of argon/PAH ratio to clustering of the PAH molecules within the argon matrix. These shifts are related to the cluster structures forming in the matrix and the topology of the monomer PAH molecule. We predict that interstellar PAH molecules that are relatively large (no fewer than 50 carbon atoms per molecule) and compact will have clusters that contribute to the asymmetrically red-shaded profile of the interstellar 11.2 μm emission band.

  8. Polycyclic Aromatic Hydrocarbons in drinking water of Tehran, Iran.

    PubMed

    Karyab, Hamid; Yunesian, Masud; Nasseri, Simin; Mahvi, Amir Hosein; Ahmadkhaniha, Reza; Rastkari, Noushin; Nabizadeh, Ramin

    2013-08-05

    Distribution and seasonal variation of sixteen priority polycyclic aromatic hydrocarbons (PAHs) were investigated in the drinking water of Tehran, the capital of Iran. Detected single and total PAHs concentrations were in the range of 2.01-38.96 and 32.45-733.10 ng/L, respectively, which were quite high compared to the values recorded in other areas of the world. The average occurrence of PAHs with high molecular weights was 79.55%; for example, chrysene occurred in 60.6% of the samples, with a maximum concentration of 438.96 ng/L. In addition, mean carcinogen to non-carcinogen PAHs ratio was 63.84. Although the concentration of benzo[a]pyrene, as an indicator of water pollution to PAHs, was lower than the guideline value proposed by World Health Organization (WHO) as well as that of Iranian National Drinking Water Standards for all of the samples, the obtained results indicated that carcinogen PAHs present in the drinking water of Tehran can cause threats to human health.

  9. DUSTY WINDS: EXTRAPLANAR POLYCYCLIC AROMATIC HYDROCARBON FEATURES OF NEARBY GALAXIES

    SciTech Connect

    McCormick, Alexander; Veilleux, Sylvain; Rupke, David S. N. E-mail: veilleux@astro.umd.edu

    2013-09-10

    Recent observations have shown the presence of dust and molecular material in galactic winds, but relatively little is known about the distribution of these outflow components. To shed some light on this issue, we have used IRAC images from the Spitzer Space Telescope archive to investigate polycyclic aromatic hydrocarbon (PAH) emission from a sample of 16 local galaxies with known winds. Our focus on nearby sources (median distance 8.6 Mpc) has revealed detailed PAH structure in the winds and allowed us to measure extraplanar PAH emission. We have identified extraplanar PAH features on scales of {approx}0.8-6.0 kpc. We find a nearly linear correlation between the amount of extraplanar PAH emission and the total infrared flux, a proxy for star formation activity in the disk. Our results also indicate a correlation between the height of extraplanar PAH emission and star formation rate surface density, which supports the idea of a surface density threshold on the energy or momentum injection rate for producing detectable extraplanar wind material.

  10. Polycyclic aromatic hydrocarbon (PAH) ecotoxicology in marine ecosystems.

    PubMed

    Hylland, Ketil

    2006-01-08

    Low levels of oil and hence polycyclic aromatic hydrocarbons (PAHs) are naturally present in the marine environment, although levels have increased significantly following human extraction and use of oil and gas. Other major anthropogenic sources of PAHs include smelters, the use of fossil fuels in general, and various methods of waste disposal, especially incineration. There are two major sources for PAHs to marine ecosystems in Norway: the inshore smelter industry, and offshore oil and gas production activities. A distinction is generally made between petrogenic (oil-derived) and pyrogenic (combustion-derived) PAHs. Although petrogenic PAHs appear to be bioavailable to a large extent, pyrogenic PAHs are often associated with soot particles and less available for uptake into organisms. There is extensive evidence linking sediment-associated PAHs to induction of phase-I enzymes, development of DNA adducts, and eventually neoplastic lesions in fish. Most studies have focused on high-molecular-weight, carcinogenic PAHs such as benzo[a]pyrene. It is less clear how two- and three-ring PAHs affect fish, and there is even experimental evidence to indicate that these chemicals may inhibit some components of the phase I system rather than produce induction. There is a need for increased research efforts to clarify biological effects of two- and three-ring PAHs, PAH mixtures, and adaptation processes in marine ecosystems.

  11. Bioavailability of polycyclic aromatic hydrocarbons in the North Sea

    SciTech Connect

    Utvik, T.I.R. . Environmental Section); Johnsen, S. )

    1999-06-15

    Semipermeable membrane devices (SPMDs) and blue mussels (Mytilus edulis) were used to determine the bioavailable fraction of polycyclic aromatic hydrocarbons (PAHs) from oil field produced water in the North Sea. The SPMDs and mussels were deployed at 5, 10, and 50 m depth; 100 and 300 m downstream the discharge point; and at a reference site 16 km away. In both SPMDs and mussels, the concentration of PAHs increased significantly toward the discharge point, with the strongest contribution from the lower molecular weight compounds (naphthalene, phenanthrene, dibenzothiophene, and their C1-C3 alkyl homologues). The relative increase in PAH concentration from the reference site to the site at 100 m was higher for mussels than for the SPMDs. The SPMDs reflect the water-soluble fraction of the PAHs, which is probably the most important route of exposure for organisms at lower trophic levels and presumably also the fraction available for uptake by a respiratory route. Residues in the mussels represent both the water-soluble and particle-bound fraction and give information about bioavailability of the PAHs for organisms at higher trophic levels. The results of this study suggest that both techniques give important information about the bioavailability of PAHs to marine organisms.

  12. Enhancement of polycyclic aromatic hydrocarbon biodegradation in the rhizosphere

    SciTech Connect

    Kim, S.C.; Banks, M.K.; Schwab, A.P.

    1994-12-31

    Polycyclic aromatic hydrocarbons (PAHs) are a class of potentially hazardous chemicals that exhibit toxic, mutagenic or carcinogenic properties. Microbial degradation is the major route through which PAHs are removed from contaminated environments although other mechanisms such as volatilization, leaching and photodegradation may also be effective. The rhizosphere contains a diversity of microorganisms that contribute to plant health and soil homeostasis. Recent studies indicate that microorganisms in the rhizosphere can degrade toxicants of concern to human health and the environment. The increased density and diversity of rhizosphere microflora may be an important factor for enhanced microbial degradation of PAHs. The objective of this study is to evaluate degradation of a number of different PAHs in rhizosphere and non-rhizosphere soil. It has been shown that the biodegradation rates of PAHs increase as the number of PAH rings decrease, but there is little information about the biodegradation in rhizosphere soil. The study will provide results from a microcosm experiment designed to evaluate degradation of PAHs in rhizosphere and non-rhizosphere. Also, kinetic models will be developed to represent data collected.

  13. Biodegradation of polycyclic aromatic hydrocarbons in rhizosphere soil

    SciTech Connect

    Schwab, A.P.; Banks, M.K.; Arunachalam, M.

    1995-12-31

    Increased contaminant biodegradation in soil in the presence of plants has been demonstrated for several classes of organic compounds. Although enhanced dissipation of polycyclic aromatic hydrocarbons (PAHs) was observed previously in the rhizosphere of several plant species, the mechanism of this effect has not been assessed. A laboratory experiment was conducted to test the importance of cometabolism and the presence of common rhizosphere organic acids on the loss of PAHs (pyrene and phenanthrene) from soil. The role of cometabolism in the mineralization of pyrene was tested by observing the impact of adding phenanthrene to soil containing {sup 14}C-pyrene and observing the effects on {sup 14}CO{sub 2} generation. Adding phenanthrene apparently induced cometabolism of pyrene, particularly in the presence of organic acids. In a subsequent experiment, mineralization of pyrene to {sup 14}CO{sub 2} was significantly greater in soil from the rhizospheres of warm-season grasses, sorghum (Sorghum bicolor L.) and bermuda grass (Cynodon dactylon L.), compared to soil from alfalfa (Medicago sativa L.), which did not differ from sterilized control soil. A highly branched, fine root system appears to be more effective in enhancing biodegradation than taproots, and the presence of organic acids increases rates of PAH mineralization.

  14. Polycyclic aromatic hydrocarbon biodegradation by a mixed bacterial culture

    SciTech Connect

    Dreyer, G.; Koenig, J.; Ringpfeil, M.

    1995-12-31

    Biodegradation of polycyclic aromatic hydrocarbons (PAHs), which are a complex mixture of organic compounds, was demonstrated using a bacterial mixed culture selected from a contaminated site by the BIOPRACT GmbH. The investigations were carried out in a laboratory fermenter using emulsified tar oil as the substrate to determine the following: (1) concentration of the single PAH and of the sum of PAHs relative to fermentation time, (2) carbon dioxide (CO{sub 2}) and oxygen (O{sub 2}) content in the outflowing air during fermentation, (3) chemical oxygen demand (COD) of the broth, and (4) toxicity of the broth before and after fermentation according to the bioluminescence test (DIN 38412, part 34/1). The results of this model experiment indicated that the investigated mixed culture is able to effectively metabolize the PAHs contained in tar oil, including the higher condensed compounds such as benzo(a)pyrene. In the first 8 days of fermentation, the PAH sum decreased to below 5% of the starting concentration connected with a five-fold reduction of the toxic effect on Vibrio fischeri. The PAH degradation rate correlated with the rate of COD decrease, the rate of evolving CO{sub 2}, and the consumption of O{sub 2}.

  15. Methanogenic biodegradation of two-ringed polycyclic aromatic hydrocarbons.

    PubMed

    Berdugo-Clavijo, Carolina; Dong, Xiaoli; Soh, Jung; Sensen, Christoph W; Gieg, Lisa M

    2012-07-01

    Polycyclic aromatic hydrocarbons (PAH) are widespread in methane-rich subsurface environments, such as oil reservoirs and fuel-contaminated aquifers; however, little is known about the biodegradation of these compounds under methanogenic conditions. To assess the metabolism of PAH in the absence of electron acceptors, a crude oil-degrading methanogenic enrichment culture was tested for the ability to biodegrade naphthalene, 1-methylnaphthalene (1-MN), 2-methylnaphthalene (2-MN), and 2, 6-dimethylnaphthalene (2, 6-diMN). When methane was measured as an indicator of metabolism, nearly 400 μmol of methane was produced in the 2-MN- and 2, 6-diMN-amended cultures relative to substrate-unamended controls, which is close to the amount of methane stoichiometrically predicted based on the amount of substrate added (51-56 μmol). In contrast, no substantial methane was produced in the naphthalene- and 1-MN-amended enrichments. In time course experiments, metabolite analysis of enrichments containing 2-MN and 2, 6-diMN revealed the formation of 2-naphthoic acid and 6-methyl-2-naphthoic acid, respectively. Microbial community analysis by 454 pyrosequencing revealed that these PAH-utilizing enrichments were dominated by archaeal members most closely affiliated with Methanosaeta and Methanoculleus species and bacterial members most closely related to the Clostridiaceae, suggesting that these organisms play an important role in the methanogenic metabolism of the substituted naphthalenes in these cultures.

  16. LARGE ABUNDANCES OF POLYCYCLIC AROMATIC HYDROCARBONS IN TITAN'S UPPER ATMOSPHERE

    SciTech Connect

    Lopez-Puertas, M.; Funke, B.; Garcia-Comas, M.; Dinelli, B. M.; Adriani, A.; D'Aversa, E.; Moriconi, M. L.; Boersma, C.; Allamandola, L. J.

    2013-06-20

    In this paper, we analyze the strong unidentified emission near 3.28 {mu}m in Titan's upper daytime atmosphere recently discovered by Dinelli et al. We have studied it by using the NASA Ames PAH IR Spectroscopic Database. The polycyclic aromatic hydrocarbons (PAHs), after absorbing UV solar radiation, are able to emit strongly near 3.3 {mu}m. By using current models for the redistribution of the absorbed UV energy, we have explained the observed spectral feature and have derived the vertical distribution of PAH abundances in Titan's upper atmosphere. PAHs have been found to be present in large concentrations, about (2-3) Multiplication-Sign 10{sup 4} particles cm{sup -3}. The identified PAHs have 9-96 carbons, with a concentration-weighted average of 34 carbons. The mean mass is {approx}430 u; the mean area is about 0.53 nm{sup 2}; they are formed by 10-11 rings on average, and about one-third of them contain nitrogen atoms. Recently, benzene together with light aromatic species as well as small concentrations of heavy positive and negative ions have been detected in Titan's upper atmosphere. We suggest that the large concentrations of PAHs found here are the neutral counterpart of those positive and negative ions, which hence supports the theory that the origin of Titan main haze layer is located in the upper atmosphere.

  17. Magnetic Beads-based Bioelectrochemical Immunoassay of Polycyclic Aromatic Hydrocarbons

    SciTech Connect

    Lin, Ying-Ying; Liu, Guodong; Wai, Chien M.; Lin, Yuehe

    2007-07-01

    A simple, rapid, and sensitive bioelectrochemical immunoassay method based on magnetic beads (MBs) has been developed to detect polycyclic aromatic hydrocarbons (PAHs). The principle of this bioassay is based on a direct competitive enzyme-linked immunosorbent assay using PAH-antibody-coated MBs and horseradish peroxidase (HRP)-labeled PAH (HRP-PAH). A magnetic process platform was used to mix and shake the samples during the immunoreactions and to separate free and unbound reagents after the liquid-phase competitive immunoreaction among PAH-antibody-coated MBs, PAH analyte, and HRP-PAH. After a complete immunoassay, the HRP tracers attached to MBs were transferred to a substrate solution containing 3, 3´, 5, 5´- tetramethylbenzidine (TMB) and hydrogen peroxide (H2O2) for electrochemical detection. The voltammetric characteristics of the substrate were investigated, and the reduction peak current of TMB was used to quantify the concentration of PAH. The different parameters, including the amount of HRP-PAH conjugates, the enzyme catalytic reaction time, and the pH of the supporting electrolyte that governs the analytical performance of the immunoassay have been studied in detail and optimized. The detection limit of 50 pg mL-1 was obtained under optimum experimental conditions. The performance of this bioelectrochemical magnetic immunoassay was successfully evaluated with tap water spiked with PAHs, indicating that this convenient and sensitive technique offers great promise for decentralized environmental applications.

  18. Sorption of polycyclic aromatic hydrocarbons to polystyrene nanoplastic.

    PubMed

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

    2016-07-01

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

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

    PubMed

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

    2016-04-01

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

  20. Association of polycyclic aromatic hydrocarbons in housewives' hair with hypertension.

    PubMed

    Wang, Bin; Li, Zhiwen; Ma, Yiqiu; Qiu, Xinghua; Ren, Aiguo

    2016-06-01

    The relationship between polycyclic aromatic hydrocarbons (PAHs) and hypertension remains a subject of debate. The aims of this study were to determine an association of concentrations of PAHs in housewives' hair with hypertension risk and the modification effect of single nucleotide polymorphisms (SNPs) related to Phase I metabolism of PAHs. We recruited 405 women for a cross-sectional study in Shanxi Province, China, including 170 with hypertension (the case group) and 235 without hypertension (the control group). We analyzed 26 individual PAHs in hair samples and the SNPs of the genes including cytochrome P450, family 1, subfamily A, polypeptide 1 (CYP1A1), CYP1A2, CYP1B1 and CYP2E1. Our results showed that seven PAHs in hair samples were measured with detection rate >70%. Only acenaphthylene was found to be associated with an increased risk of hypertension with adjustment for the potential confounders following Bonferroni correction, whereas others not. No SNPs of the concerned genes were found to be associated with the risk of hypertension. A multiple interaction effect of PAHs in housewives' hair and SNPs on hypertension risk was not observed. It was concluded that PAHs tended to contribute to the formation of hypertension.

  1. Measurement of polycyclic aromatic hydrocarbon (PAHs) in interplanetary dust particles

    NASA Technical Reports Server (NTRS)

    Clemett, S. J.; Maechling, C. R.; Zare, R. N.; Swan, P. D.; Walker, R. M.

    1993-01-01

    We report here the first definitive measurements of specific organic molecules (polycyclic aromatic hydrocarbons (PAH's)) in interplanetary dust particles (IDP's). An improved version of the microbeam-two-step laser mass spectrometer was used for the analysis. Two IDP's gave similar mass spectra showing an abundance of PAH's. Control samples, including particles of probable terrestrial origin from the same stratospheric collector, gave either null results or quite different spectra. We conclude that the PAH's are probably indigenous to the IDP's and are not terrestrial contaminants. The instrument used to study the particles is a two-step laser mass spectrometer. Constituent neutral molecules of the sample are first desorbed with a pulsed infrared laser beam focussed to 40 micrometers. In the second step, PAH's in the desorbed plume are preferentially ionized by a pulsed UV laser beam. Resulting ions produced by resonant absorption are extracted into a reflectron time-of-flight mass spectrometer. This instrument has high spatial resolution, high ion transmission, unlimited mass range, and multichannel detection of all ion masses from a single laser shot.

  2. Peripherally hydrogenated neutral polycyclic aromatic hydrocarbons as carriers of the 3 micron interstellar infrared emission complex: results from single-photon infrared emission spectroscopy.

    PubMed

    Wagner, D R; Kim, H S; Saykally, R J

    2000-12-20

    Infrared emission spectra of five gas-phase UV laser-excited polycyclic aromatic hydrocarbons (PAHs) containing aliphatic hydrogens are compared with the main 3.3 microns and associated interstellar unidentified infrared emission bands (UIRs). We show that neutral PAHs can account for the majority of the 3 microns emission complex while making little contribution to the other UIR bands; peripherally hydrogenated PAHs produce a better match to astrophysical data than do those containing methyl side groups; 3.4 microns plateau emission is shown to be a general spectral feature of vibrationally excited PAHs containing aliphatic hydrogens, especially those containing methyl groups; and finally, hot-band and overtone emissions arising from aromatic C-H vibrations are not observed in laboratory emission spectra, and therefore, in contrast to current assignments, are not expected to be observed in the UIRs.

  3. Peripherally hydrogenated neutral polycyclic aromatic hydrocarbons as carriers of the 3 micron interstellar infrared emission complex: results from single-photon infrared emission spectroscopy

    NASA Technical Reports Server (NTRS)

    Wagner, D. R.; Kim, H. S.; Saykally, R. J.

    2000-01-01

    Infrared emission spectra of five gas-phase UV laser-excited polycyclic aromatic hydrocarbons (PAHs) containing aliphatic hydrogens are compared with the main 3.3 microns and associated interstellar unidentified infrared emission bands (UIRs). We show that neutral PAHs can account for the majority of the 3 microns emission complex while making little contribution to the other UIR bands; peripherally hydrogenated PAHs produce a better match to astrophysical data than do those containing methyl side groups; 3.4 microns plateau emission is shown to be a general spectral feature of vibrationally excited PAHs containing aliphatic hydrogens, especially those containing methyl groups; and finally, hot-band and overtone emissions arising from aromatic C-H vibrations are not observed in laboratory emission spectra, and therefore, in contrast to current assignments, are not expected to be observed in the UIRs.

  4. Microbial community structure of a heavy fuel oil-degrading marine consortium: linking microbial dynamics with polycyclic aromatic hydrocarbon utilization.

    PubMed

    Vila, Joaquim; María Nieto, José; Mertens, Jelle; Springael, Dirk; Grifoll, Magdalena

    2010-08-01

    A marine microbial consortium obtained from a beach contaminated by the Prestige oil spill proved highly efficient in removing the different hydrocarbon families present in this heavy fuel oil. Seawater cultures showed a complete removal of all the linear and branched alkanes, an extensive attack on three to five-ring polycyclic aromatic hydrocarbons [PAHs; including anthracene, fluoranthene, pyrene, benzo(a)anthracene, chrysene, and benzo(a)pyrene] (30-100%), and a considerable depletion of their alkyl derivatives. Community dynamics analysis revealed that Alcanivorax species, known alkane degraders, predominated in the initial stages. This was followed by an increase in Alphaproteobacteria (i.e. Maricaulis, Roseovarius), which coincided with the depletion of low molecular PAHs. Finally, these were succeeded by Gammaproteobacteria (mainly Marinobacter and Methylophaga), which were involved in the degradation of the high molecular-weight PAHs. The role of these populations in the removal of the specific components was confirmed by the analysis of subcultures established using the aliphatic or the aromatic fraction of the fuel oil, or single PAHs, as carbon sources. The genus Marinobacter seemed to play a major role in the degradation of a variety of hydrocarbons, as several members of this group were isolated from the different enrichment cultures and grew on plates with hexadecane or single PAHs as sole carbon sources.

  5. Trace elements, organochlorines, polycyclic aromatic hydrocarbons, dioxins, and furans in lesser scaup wintering on the Indiana Harbor Canal

    USGS Publications Warehouse

    Custer, T.W.; Custer, Christine M.; Hines, R.K.; Sparks, D.W.

    2000-01-01

    During the winter of 1993a??94, male lesser scaup (Aythya affinis) were collected on the heavily polluted Indiana Harbor Canal (IHC), East Chicago, IN, USA, and examined for tissue contaminant levels. Lesser scaup collected on the IHC had higher concentrations of cadmium (Cd), mercury (Hg), selenium (Se), polychlorinated biphenyls (PCBs), selected organchlorine pesticides, polychlorinated dibenzodioxins, polychlorinated dibenzofurans, polycyclic aromatic hydrocarbons, and aliphatic hydrocarbons than reference birds. Of the scaup collected on the IHC, 44% had Cd concentrations in the liver considered above background for freshwater waterfowl (>3 I?g/g dry wt.), 50% had Se concentrations in the liver above a level possibly harmful to the health of young and adult birds (>33 I?g/g dry wt.), and 88% of the scaup carcasses exceeded the PCB human consumption guidelines for edible poultry in the USA (>3.0 I?g/g lipid wt.). The ratio of pristane:n-heptadecane concentrations in 47% of lesser scaup collected on IHC was elevated above 1.0, which is indicative of chronic exposure to petroleum hydrocarbons. Copyright A? 2009 Elsevier B.V.

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

    PubMed

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

    2015-03-01

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

  7. Trace level determination of polycyclic aromatic hydrocarbons in river water with automated pretreatment HPLC.

    PubMed

    Watabe, Yoshiyuki; Kubo, Takuya; Tanigawa, Tetsuya; Hayakawa, Yoshihiro; Otsuka, Koji; Hosoya, Ken

    2013-03-01

    A novel on-line pretreatment pump-injection HPLC system for polycyclic aromatic hydrocarbons is proposed. We report novel pump-injection HPLC-based on-line SPE with a specially designed pretreatment column for the determination of trace amounts of chemical substances in surface water. Polycyclic aromatic hydrocarbons are well known for strong carcinogenicity and thus a severe concentration control is required for drinking water and/or river water, which is the main resource of tap water. We found it possible to detect ng/L levels of polycyclic aromatic hydrocarbons by using pump-injection column switching HPLC with fluorescence detection. To avoid the phenomenon, in which polycyclic aromatic hydrocarbons can be often adsorbed on the surface of flow lines of HPLC by their highly hydrophobicity especially resin-made parts in sample delivery pump, we employed "autodilution" device that provides reliable recovery and repeatability. Additionally, real water samples were collected and then the spiked polycyclic aromatic hydrocarbons were determined at ng/L levels.

  8. Sorption of polycyclic aromatic hydrocarbons (PAHs) on glass surfaces.

    PubMed

    Qian, Yuan; Posch, Tjorben; Schmidt, Torsten C

    2011-02-01

    Sorption of polycyclic aromatic hydrocarbons (PAHs) to glass commonly used in laboratories was studied. Sorption coefficients (Kd) of five selected PAHs to borosilicate glass surfaces were measured using column chromatography. A linear relationship between log Kd and the corresponding water solubility of the subcooled liquid (log Sw) of the investigated PAHs was observed. Based on the determined sorption coefficients our data revealed that mass loss caused by sorption on glass walls strongly depends on the ratio of solution volume to contacted surface area (V/S). The influence of solution chemistry such as ionic strength, solution pH, presence of cosolvent, and the influence of temperature on the sorption process were investigated. In the presence of ionic strength, sorption coefficients concurrently increased but less than a factor of 2 up to 0.005 M calcium chloride concentration. However, further increasing ionic strength had no influence on Kd. The cosolvent reduced sorption at a concentration of methanol in water above 0.5% (v/v); however, for benzo[a]pyrene even with 10% (v/v) methanol the mass loss would be still higher than 10% (with a V/S ratio less than 0.25). Significant effects of the solution pH and temperature were not observed. These results suggest that van der Waal's forces dominate the sorption process. In the analysis of highly hydrophobic PAHs in aqueous samples, mass loss due to sorption on glass walls should be accounted for in the final result if untreated glass is used. The presented relationship between log Kd and log Sw may help to decide if such a correction is necessary. Furthermore, the frequently used silanization of glass surfaces may not be sufficient to suppress sorption for large PAHs.

  9. Intraperitoneal mesotheliomas induced in mice by a polycyclic aromatic hydrocarbon

    SciTech Connect

    Rice, J.M.; Anderson, L.M. ); Kovatch, R.M. )

    1989-01-01

    Female mice of 6 strains (C3H/HeN, BALB/c, C57BL/6N, DBA/2, NIH Swiss, and AKR/N) were given the polycyclic aromatic hydrocarbon carcinogen 3-methylcholanthrene (MC) intragastrically in olive oil at a dose of 20 mg/kg, weekly for 12 wk. Half were pretreated 24 h before each MC administration with intraperitoneal {beta}-naphthoflavone ({beta}-NF, 150 mg/kg in olive oil), a noncarinogenic inducer of certain cytochrome P-450 isozymes. Remaining mice were given olive oil prior to MC in the same fashion, or {beta}-NF in olive oil or olive oil alone without subsequent exposure to MC. All mice were killed when moribund or 13 mo after the start of treatment. Most of the mice, irrespective of treatment, exhibited signs of peritoneal injury, including inflammation, necrosis, granuloma formation, and mineralization. Mice of some of the strains also presented peritoneal mesotheliomas, in addition to a variety of other tumors. {beta}-NF pretreatment reduced the frequency of mesotheliomas: there was only one definite mesothelioma in any of the {beta}-NF-MC groups, in a C3H/He mouse. Most of the measotheliomas were mixed fibro-mesothelial type, sometimes with papillary epithelial excrescences. They typically grew in a botryoid pattern within the peritoneal cavity, coating the abdominal organs and sometimes actively invading these organs and the diaphragm. Some lesions exhibited pleomorphism, prominent giant cells, and frequent mitoses. In addition, several lesions consisting of severe mesothelial hyperplasia associated with tissue necrosis and inflammation were considered as possible early stages of mesothelioma development. It was postulated that peritoneal injury imposed by repeated intraperitoneal injection of oil acted as an enhancing factor for mesothelioma induction by MC.

  10. Tracing Star Formation Around Quasars With Polycyclic Aromatic Hydrocarbons

    NASA Astrophysics Data System (ADS)

    Bilton, Lawrence Edward

    2016-09-01

    The feedback processes linking quasar activity to galaxy stellar mass growth are not well understood. If star formation is closely causally linked to black hole accretion, one may expect star formation confined to nuclear regions rather than extended over several kpc scales. Since Polycyclic Aromatic Hydrocarbon (PAH) emission features are widely used as tracers of stellar formation, it is, therefore, possible to use PAH emission detected around QSOs to help resolve this question. PAH data from a sample of 63 QSOs procured from the Spitzer Space Telescope’s Infrared Spectrograph (IRS) is used, employing the Spectroscopic Modelling Analysis and Reduction Tool’s (SMART) Advanced Optimal (AdOpt) extraction routines. A composite spectrum was also produced to help determine the average conditions and compositions of star forming regions. It is found, from our high redshift (>1) sample of QSOs, there is a marginally significant extended star formation on average of 34 scales. At low redshift, the median extension after deconvolving the instrumental point spread function is 3.2 , potentially showing evolutionary variations in star formation activity. However, limitations of the spatial resolving power constrain the ability to make any absolute conclusive remarks. It is also found that the QSO/AGN composite has more neutral PAHs than the starbursting and the main sequence galaxies, consistent with the AGN having no contribution to heating the PAH emission, and also consistent with the average PAH emission found on scales (i.e. not confined to the nuclear regions). A tentative detection of water vapour emission from the gravitationally lensed Einstein Cross quasar, QSO J2237+0305, is also presented suggesting a strong molecular outflow possibly driven by the active nucleus.

  11. Polycyclic aromatic hydrocarbon ecotoxicity data for developing soil quality criteria.

    PubMed

    Jensen, John; Sverdrup, Line E

    2003-01-01

    With the overall perspective of calculating soil quality criteria (SQC) for the group of polycyclic aromatic hydrocarbons (PAHs), the existing ecotoxicity data for the soil compartment have been reviewed. The majority of data useful in the context of deriving SQC are of recent origin. Soil quality criteria are considered valuable tools for assessing the environmental risk of contamination, as they may give guidance on concentration limits for various chemicals to protect the function and structure of ecosystems. Soil quality criteria for soil-dwelling species were calculated using various assumptions and two internationally accepted methods, i.e., application of assessment factors and species sensitivity distributions, respectively. It was suggested to derive ecotoxicological soil quality criteria, which focus on the lower molecular weight PAHs, i.e., those with log Kow values lower than 5.5 or 6; this is the log Kow range where a cutoff in toxicity for terrestrial species is expected for narcotic substances. Predicted values from the two methods were similar. Calculations showed that, for four individual PAHs of three or four rings, SQC fall in the range of 1.0 and 2.5 mg kg(-1). However, as no individual PAH is fond alone it is suggested to use a sum criterion for a group of PAHs instead. The different possibilities to calculate such a sum criterion are discussed. Based on toxicity data presented here and the average abundance of different PAHs in nearly 1000 Danish soil samples, an ecotoxicological soil quality criterion of 25 mg kg(-1) dry weight for the sum of the eight PAHs acenaphthene, fluorene, anthracene, phenanthrene, pyrene, fluoranthene, benz[a]anthracene, and chrysene is suggested.

  12. Human colon microbiota transform polycyclic aromatic hydrocarbons to estrogenic metabolites.

    PubMed

    Van de Wiele, Tom; Vanhaecke, Lynn; Boeckaert, Charlotte; Peru, Kerry; Headley, John; Verstraete, Willy; Siciliano, Steven

    2005-01-01

    Ingestion is an important exposure route for polycyclic aromatic hydrocarbons (PAHs) to enter the human body. Although the formation of hazardous PAH metabolites by human biotransformation enzymes is well documented, nothing is known about the PAH transformation potency of human intestinal microbiota. Using a gastrointestinal simulator, we show that human intestinal microbiota can also bioactivate PAHs, more in particular to estrogenic metabolites. PAH compounds are not estrogenic, and indeed, stomach and small intestine digestions of 62.5 nmol naphthalene, phenanthrene, pyrene, and benzo(a)pyrene showed no estrogenic effects in the human estrogen receptor bioassay. In contrast, colon digests of these PAH compounds displayed estrogenicity, equivalent to 0.31, 2.14, 2.70, and 1.48 nmol 17alpha-ethynylestradiol (EE2), respectively. Inactivating the colon microbiota eliminated these estrogenic effects. Liquid chromatography-mass spectrometry analysis confirmed the microbial PAH transformation by the detection of PAH metabolites 1-hydroxypyrene and 7-hydroxybenzo(a)pyrene in colon digests of pyrene and benzo(a)pyrene. Furthermore, we show that colon digests of a PAH-contaminated soil (simulated ingestion dose of 5 g/day) displayed estrogenic activity equivalent to 0.58 nmol EE2, whereas stomach or small intestine digests did not. Although the matrix in which PAHs are ingested may result in lower exposure concentrations in the gut, our results imply that the PAH bioactivation potency of colon microbiota is not eliminated by the presence of soil. Moreover, because PAH toxicity is also linked to estrogenicity of the compounds, the PAH bioactivation potency of colon microbiota suggests that current risk assessment may underestimate the risk from ingested PAHs.

  13. Generation of polycyclic aromatic hydrocarbons (PAHs) during woodworking operations

    PubMed Central

    Bruschweiler, Evin D.; Danuser, Brigitta; Huynh, Cong Khanh; Wild, Pascal; Schupfer, Patrick; Vernez, David; Boiteux, Philippe; Hopf, Nancy B.

    2012-01-01

    Occupational exposures to wood dust have been associated with an elevated risk of sinonasal cancer (SNC). Wood dust is recognized as a human carcinogen but the specific cancer causative agent remains unknown. One possible explanation is a co-exposure to; wood dust and polycyclic aromatic hydrocarbons (PAHs). PAHs could be generated during incomplete combustion of wood due to heat created by use of power tools. To determine if PAHs are generated from wood during common wood working operations, PAH concentrations in wood dust samples collected in an experimental chamber operated under controlled conditions were analyzed. In addition, personal air samples from workers exposed to wood dust (n = 30) were collected. Wood dust was generated using three different power tools: vibrating sander, belt sander, and saw; and six wood materials: fir, Medium Density Fiberboard (MDF), beech, mahogany, oak and wood melamine. Monitoring of wood workers was carried out by means of personal sampler device during wood working operations. We measured 21 PAH concentrations in wood dust samples by capillary gas chromatography-ion trap mass spectrometry (GC-MS). Total PAH concentrations in wood dust varied greatly (0.24–7.95 ppm) with the lowest being in MDF dust and the highest in wood melamine dust. Personal PAH exposures were between 37.5–119.8 ng m−3 during wood working operations. Our results suggest that PAH exposures are present during woodworking operations and hence could play a role in the mechanism of cancer induction related to wood dust exposure. PMID:23087908

  14. Infrared Spectroscopy of Polycyclic Aromatic Hydrocarbon Cations. 3; The Members

    NASA Technical Reports Server (NTRS)

    Hudgins, D. M.; Allamandola, L. J.; Wittebon, Fred C. (Technical Monitor)

    1994-01-01

    In spite of the fact that the infrared spectroscopic properties of only a few isolated ionized polycyclic aromatic hydrocarbons (PAHs) are known, gaseous, ionized PAHs are thought to be responsible for a very common family of infrared interstellar emission bands. In order to provide a data base to test this hypothesis and, if borne out, to use this emission band family as a probe of many different interstellar environments, we are carrying out a thorough study of the infrared spectroscopic properties of neutral and ionized PAHs in argon matrices. Here we present the near and mid-infrared spectra of the cations of the five most thermodynamically favored PAHs up to coronene: phenanthrene, pyrene, benzo[e]pyrene, benzo[ghilperylene, and coronene. The properties of naphthalene, the first member of the series, are given elsewhere. The spectra of perdeuterated phenanthrene and pyrene are also reported. For those molecules which have been previously studied (pyrene, d(10)-pyrene, and coronene), band positions and relative intensities are in agreement. In all cases we report additional features. Absolute integrated absorbance values are given for the phenanthrene, perdeutero-phenanthrene, pyrene, benzo[ghi]perylene, and coronene cations. With the exception of coronene,the cation bands corresponding to the CC modes are typically 2-5 times more intense than those of the CH out-of-plane bending vibrations. For the cations the CC stretching and CH in-plane bending modes give rise to bands which are an order of magnitude stronger than for the neutral species, and the CH out-of-plane bends produce bands which are 5-20 times weaker than in the neutral species. This behavior is similar to that found in most other PAH cations studied to date. The astronomical implications of these PAH cation spectra are also discussed.

  15. STRONG POLYCYCLIC AROMATIC HYDROCARBON EMISSION FROM z {approx} 2 ULIRGs

    SciTech Connect

    Desai, Vandana; Soifer, B. T.; Melbourne, Jason; Dey, Arjun; Brand, Kate; Brodwin, Mark; Jannuzi, Buell T.; Le Floc'h, Emeric; Armus, Lee; Teplitz, Harry; Brown, Michael J. I.; Houck, James R.; Weedman, Daniel W.; Ashby, Matthew L. N.; Huang Jiasheng; Smith, Howard A.; Willner, Steve P.; Gonzalez, Anthony

    2009-08-01

    Using the Infrared Spectrograph on board the Spitzer Space Telescope, we present low-resolution (64 < {lambda}/{delta}{lambda} < 124), mid-infrared (20-38 {mu}m) spectra of 23 high-redshift ULIRGs detected in the Booetes field of the NOAO Deep Wide-Field Survey. All of the sources were selected to have (1) f {sub {nu}}(24 {mu}m)>0.5 mJy; (2) R - [24]>14 Vega mag; and (3) a prominent rest frame 1.6 {mu}m stellar photospheric feature redshifted into Spitzer's 3-8 {mu}m IRAC bands. Of these, 20 show emission from polycyclic aromatic hydrocarbons (PAHs), usually interpreted as signatures of star formation. The PAH features indicate redshifts in the range 1.5 < z < 3.0, with a mean of (z) = 1.96 and a dispersion of 0.30. Based on local templates, these sources have extremely large infrared luminosities, comparable to that of submillimeter galaxies. Our results confirm previous indications that the rest-frame 1.6 {mu}m stellar bump can be efficiently used to select highly obscured star-forming galaxies at z {approx} 2, and that the fraction of starburst-dominated ULIRGs increases to faint 24 {mu}m flux densities. Using local templates, we find that the observed narrow redshift distribution is due to the fact that the 24 {mu}m detectability of PAH-rich sources peaks sharply at z = 1.9. We can analogously use observed spectral energy distributions to explain the broader redshift distribution of Spitzer-detected ULIRGs that are dominated by an active galactic nucleus (AGN). Finally, we conclude that z {approx} 2 sources with a detectable 1.6 {mu}m stellar opacity feature lack sufficient AGN emission to veil the 7.7 {mu}m PAH band.

  16. Polycyclic Aromatic Hydrocarbons in Residential Dust: Sources of Variability

    PubMed Central

    Metayer, Catherine; Petreas, Myrto; Does, Monique; Buffler, Patricia A.; Rappaport, Stephen M.

    2013-01-01

    Background: There is interest in using residential dust to estimate human exposure to environmental contaminants. Objectives: We aimed to characterize the sources of variability for polycyclic aromatic hydrocarbons (PAHs) in residential dust and provide guidance for investigators who plan to use residential dust to assess exposure to PAHs. Methods: We collected repeat dust samples from 293 households in the Northern California Childhood Leukemia Study during two sampling rounds (from 2001 through 2007 and during 2010) using household vacuum cleaners, and measured 12 PAHs using gas chromatography–mass spectrometry. We used a random- and a mixed-effects model for each PAH to apportion observed variance into four components and to identify sources of variability. Results: Median concentrations for individual PAHs ranged from 10 to 190 ng/g of dust. For each PAH, total variance was apportioned into regional variability (1–9%), intraregional between-household variability (24–48%), within-household variability over time (41–57%), and within-sample analytical variability (2–33%). Regional differences in PAH dust levels were associated with estimated ambient air concentrations of PAH. Intraregional differences between households were associated with the residential construction date and the smoking habits of residents. For some PAHs, a decreasing time trend explained a modest fraction of the within-household variability; however, most of the within-household variability was unaccounted for by our mixed-effects models. Within-household differences between sampling rounds were largest when the interval between dust sample collections was at least 6 years in duration. Conclusions: Our findings indicate that it may be feasible to use residential dust for retrospective assessment of PAH exposures in studies of health effects. PMID:23461863

  17. Partition of polycyclic aromatic hydrocarbons on organobentonites from water.

    PubMed

    Chen, B L; Zhu, L Z

    2001-04-01

    A series of organobentonites synthesized by exchanging organic cation such as dodecyltri-methylammonium (DTMA), benzyldimethyltetradecylammonium (BDTDA), cetyltrimethyl-ammonium (CTMA), octodeyltrimethylammonium (OTMA) on bentonite. The optimal condition, properties and mechanisms for the organobentonites to sorb phenanthrene, anthracene, naphthalene, acenaphthene in water were investigated in detail. The partition behavior was determined for four polycyclic aromatic hydrocarbons (PAHs), such as naphthalene, phenanthrene, anthracene and acenaphthene, from water to a series of organobentonites. The interlayer spacings and organic carbon contents of organobentonites, removal rate and sorption capacities for organobentonites to treat phenanthrene, anthracene, naphthalene, acenaphthene were correlated to the length of alkyl chains and the amounts of cation surfactant exchanged on the bentonite. Phenanthrene, anthracene, naphthalene, and acenaphthene sorption to organobentonites were characterized by linear isotherms, indicating solute partition between water and the organic phase composed of the large alkyl functional groups of quaternary ammonium cations. PAHs distribution coefficients (Kd) between organobentonites and water were proportional to the organic carbon contents of organobentonites. However, the partition coefficients (Koc) were nearly constants for PAHs in the system of organobentonite-water. The Koc of phenanthrene, anthracene, naphthalene, acenaphthene were 2.621 x 10(5), 2.106 x 10(5), 2.247 x 10(4), 5.085 x 10(4), respectively. The means Koc values on the organobentonites are about ten to twenty times larger than the values on the soils/sediments, what is significant prerequisite for organobentonite to apply to remediation of pollution soil and groundwater. The sorption mechanism was also evaluated from octanol-water partition coefficients and aqueous solubility of PAHs. The correlations between 1gKoc and 1gKow, 1gKoc and 1gS for PAHs in the system of

  18. Characterization of polycyclic aromatic hydrocarbons in fog-rain events.

    PubMed

    Li, Xiang; Li, Pengfei; Yan, Lili; Chen, Jianmin; Cheng, Tiantao; Xu, Shifen

    2011-11-01

    Atmospheric polycyclic aromatic hydrocarbons (PAHs) mainly originate from incomplete combustion or pyrolysis of materials containing carbon and hydrogen. They exist in gas and particle phases, as well as dissolved or suspended in precipitation (fog or rain). Current studies in atmospheric PAHs are predominantly focused on fog and rainwater samples. Some sampling difficulties are associated with fog samples. This study presented the first observation of the characteristics of PAHs in fog samples using a solid phase microextraction (SPME) technique. Eighteen fog samples were collected during ten fog events from March to December 2009 in the Shanghai area. PAHs were extracted by SPME and analyzed by gas chromatography-mass spectrometry (GC-MS). As the compounds were partially soluble in water, with solubility decreasing with increasing molecular weight, low molecular weight (LMW) PAH compounds were universally found in the fog water samples. Naphthalene (NaP), phenanthrene (Phe), anthracene (Ant) and fluoranthene (Flo) were dominant compounds in fog water. The total PAH concentration in fog water ranged from 0.03 to 6.67 μg L(-1) (mean of 1.06 μg L(-1)), and was much higher in winter than in summer. The concentration of PAHs in fog or rain water decreased after undergoing a pre-rain or pre-fog wash. The average concentration of PAHs was higher in fog than in rain. Diagnostic ratio analysis suggested that petroleum and combustion were the dominant contributors to PAHs in urban Shanghai. Backward trajectories were calculated to determine the origin of the air masses, showing that air masses were mostly from the northeast territory.

  19. Polycyclic aromatic hydrocarbons in mountain soils of the subtropical Atlantic.

    PubMed

    Ribes, A; Grimalt, J O; Torres García, C J; Cuevas, E

    2003-01-01

    Surface soil samples from various altitudes on Tenerife Island, ranging from sea level up to 3400 m above mean sea level, were analyzed to study the distribution of 26 polycyclic aromatic hydrocarbons (PAHs) in a remote subtropical area. The stable atmospheric conditions in this island define three vertically stratified layers: marine boundary, trade-wind inversion, and free troposphere. Total PAH concentrations, 1.9 to 6000 microg/kg dry wt., were high when compared with those in tropical areas and in a similar range to those in temperate areas. In the marine boundary layer, fluoranthene (Fla), pyrene (Pyr), benz [a]anthracene (BaA), and chrysene (C + T) were largely dominant. The predominance of Fla over Pyr may reflect photo-oxidative processes during atmospheric transport, although coal combustion inputs cannot be excluded. The PAHs found in higher concentration in the soils from the inversion layer were benzo[b + j]fluoranthene (BbjF) + benzo[k]fluoranthene (BkF) > benzo[e]pyrene (BeP) approximately indeno[1,2, 3-cd]pyrene (Ind) > benzo[a]pyrene (BaP) approximately benzo[ghi]perylene (Bghi) > coronene (Cor) approximately dibenz[a,h]anthracene (Dib), reflecting that high temperatures and insolation prevent the accumulation of PAHs more volatile than BbjF in significant amounts. These climatic conditions involve a process of standardization that prevents the identification of specific PAH sources such as traffic, forest fires, or industrial inputs. Only soils with high total organic carbon (TOC) (e.g., 10-30%) preserve the more volatile compounds such as phenanthrene (Phe), methylphenanthrenes (MPhe), dimethylphenanthrenes (DMPhe), and retene (Ret). However, no relation between PAHs and soil TOC and black carbon (BC) was found. The specific PAH distributions of the free tropospheric region suggest a direct input from pyrolytic processes related to the volcanic emission of gases in Teide.

  20. Polycyclic Aromatic Hydrocarbons and digestive tract cancers - a perspective

    PubMed Central

    Diggs, Deacqunita L.; Huderson, Ashley C.; Harris, Kelly L.; Myers, Jeremy N.; Banks, Leah D.; Rekhadevi, Perumalla V.; Niaz, Mohammad S.; Ramesh, Aramandla

    2011-01-01

    Cancers of the colon are most common in the Western world. In majority of these cases, there is no familial history and sporadic gene damage seems to play an important role in the development of tumors in the colon. Studies have shown that environmental factors, especially diet, play an important role in susceptibility to GI tract cancers. Consequently, environmental chemicals that contaminate food or diet during its preparation becomes important in the development of GI cancers. Polycyclic aromatic hydrocarbons (PAHs) are one such family of ubiquitous environmental toxicants. These pollutants enter the human body through consumption of contaminated food, drinking water, inhalation of cigarette smoke, automobile exhausts, and contaminated air from occupational settings. Among these pathways, dietary intake of PAHs constitutes a major source of exposure in humans. Although many reviews and books on PAHs and their ability to cause toxicity and breast or lung cancer have been published, aspects on contribution of diet, smoking and other factors towards development of digestive tract cancers and strategies to assess risk from exposure to PAHs have received much less attention. This review, therefore, focuses on dietary intake of PAHs in humans, animal models, and cell cultures used for GI cancer studies along with epidemiological findings. Bioavailability and biotransformation processes, which influence the disposition of PAHs in body and the underlying causative mechanisms of GI cancers, are also discussed. The existing data gaps and scope for future studies is also emphasized. This information is expected to stimulate research on mechanisms of sporadic GI cancers caused by exposure to environmental carcinogens. PMID:22107166

  1. Fluorescence Spectroscopy of Gas-phase Polycyclic Aromatic Hydrocarbons

    NASA Technical Reports Server (NTRS)

    Thomas, J. D.; Witt, A. N.

    2006-01-01

    The purpose of this investigation was to produce fluorescence spectra of polycyclic aromatic hydrocarbon (PAH) molecules in the gas-phase for comparison with blue luminescence (BL) emission observed in astrophysical sources Vijh et al. (2004, 2005a,b). The BL occurs roughly from 350 to 450 nm, with a sharp peak near 380 nm. PAHs with three to four rings, e.g. anthracene and pyrene, were found to produce luminescence in the appropriate spectral region, based on existing studies. Relatively few studies of the gas-phase fluorescence of PAHs exist; those that do exist have dealt primarily with the same samples commonly available for purchase such as pyrene and anthracene. In an attempt to understand the chemistry of the nebular environment we also obtained several nitrogen substituted PAHs from our colleagues at NASA Ames. In order to simulate the astrophysical environment we also took spectra by heating the PAHs in a flame. The flame environment counteracts the formation of eximers and permits the spectroscopy of free-flying neutral molecules. Experiments with coal tar demonstrate that fluorescence spectroscopy reveals primarily the presence of the smallest molecules, which are most abundant and which possess the highest fluorescence efficiencies. One gas-phase PAH that seems to fit the BL spectrum most closely is phenanthridine. In view of the results from the spectroscopy of coal tar, a compound containing a mixture of PAHs ranging from small to very large PAH molecules, we can not preclude the presence of larger PAHs in interstellar sources exhibiting BL.

  2. Ambient polycyclic aromatic hydrocarbons and pulmonary function in children

    PubMed Central

    Padula, Amy M.; Balmes, John R.; Eisen, Ellen A.; Mann, Jennifer; Noth, Elizabeth M.; Lurmann, Frederick W.; Pratt, Boriana; Tager, Ira B.; Nadeau, Kari; Hammond, S. Katharine

    2014-01-01

    Few studies have examined the relationship between ambient polycyclic aromatic hydrocarbons (PAHs) and pulmonary function in children. Major sources include vehicular emissions, home heating, wildland fires, agricultural burning, and power plants. PAHs are an important component of fine particulate matter that has been linked to respiratory health. This cross-sectional study examines the relationship between estimated individual exposures to the sum of PAHs with 4, 5, or 6 rings (PAH456) and pulmonary function tests (forced expiratory volume in one second (FEV1) and forced expiratory flow between 25% and 75% of vital capacity) in asthmatic and non-asthmatic children. We applied land-use regression to estimate individual exposures to ambient PAHs for averaging periods ranging from 1 week to 1 year. We used linear regression to estimate the relationship between exposure to PAH456 with pre- and postbronchodilator pulmonary function tests in children in Fresno, California (N =297). Among non-asthmatics, there was a statistically significant association between PAH456 during the previous 3 months, 6 months, and 1 year and postbronchodilator FEV1. The magnitude of the association increased with the length of the averaging period ranging from 60 to 110 ml decrease in FEV1 for each 1 ng/m3 increase in PAH456. There were no associations with PAH456 observed among asthmatic children. We identified an association between annual PAHs and chronic pulmonary function in children without asthma. Additional studies are needed to further explore the association between exposure to PAHs and pulmonary function, especially with regard to differential effects between asthmatic and non-asthmatic children. PMID:24938508

  3. [Desorption of polycyclic aromatic hydrocarbons in soils assisted by SPMD].

    PubMed

    Sun, Hong-Wen; Huo, Chong; Wang, Cui-Ping

    2007-08-01

    In order to develop a new method to study the desorption and bioavailability of hydrophobic organic chemicals (HOCs) in soils, a method using semi-permeable membrane device (SPMD) to study desorption of HOCs in soils has been set up, and assisted desorption of polycyclic aromatic hydrocarbons (PAHs), phenanthrene(PHE), pyrene(PYE), and benzo[a] pyrene (B[a]PYE) in three different kinds of soils was studied using SPMD. The results show that SPMD is a good measurement to study the desorption and bioavailability of HOCs in soils. SPMD assisted desorption of PAHs is highly dependent on the properties of the soils and the chemicals. PHE and PYE desorption percentages increase with the reduction of the content of soil organic matter (SOM), so that the desorption of the two chemicals increases from 56.45% and 48.28% to almost 100% when SOM content was reduced from 18.68% to 0.3%. However, clay has a significant holding effect on B[a]PYE, and PYE desorption is only 66.97% in Soil 3 with SOM of 0.3% and clay content of 39.05%. There is a great variety in the desorption among the different PAHs. With the reduction of SOM content and the elevation of contamination concentration, the difference between PHE and PYE decreases gradually, while B[a]PYE exhibits a significant difference from them. This could be attributed to the high lipophilicity and large molecular size of B[a]PYE, which make the molecule of B[a]PYE to be more easier to be held in the nanopores of clay and the dense region of SOM.

  4. Exposure to polycyclic aromatic hydrocarbons among Dutch children

    SciTech Connect

    Wijnen, J.H. van; Slob, R.; Jongmans-Liedekerken, G.

    1996-05-01

    We determined the urinary 1-hydroxypyrene (1-HP) concentration and the creatinine-adjusted 1-HP concentration in 644 randomly selected Dutch children, aged 1-6 years and living in five areas with roughly different levels of polycyclic aromatic hydrocarbons (PAHs) in soil and ambient air. The presence of other factors that might influence the exposure to PAHs was studied using a questionnaire. To evaluate the reliability of a single urinary 1-HP determination, measurements were repeated after 3 weeks for approximately 200 children. The mean urinary 1-HP content of the total study population was 2.06 nmol/1. This varied from 1.58 nmol/l in the reference area (Flevoland) to 2.71 nmol/l in the valley of the Geul. Only indoor sources of PAHs showed a small, positive association with urinary 1-HP. The urinary 1-HP concentrations of children from the valley of the Geul were higher (p<0.01) and those of children from a suburb of Amsterdam were lower (p<0.01) than those of children from the reference area. The possible ambient environment-related differences were probably too small to be detected in the variations of the intake of PAHs from the daily diet. The reliability of a single 1-HP measurement was low. Similar results were obtained with the creatinine-adjusted data. In one neighborhood built on coal-mine tailings, the urinary 1-HP content in children was weakly but positively associated with the PAH content in the upper soil layer of the garden of their homes. However, this association was not found for the children from the other neighborhood built on coal-mine tailings and with similar PAH levels in soil. 25 refs., 4 tabs.

  5. Simulation of polycyclic aromatic hydrocarbons transport in multimedia

    SciTech Connect

    Chen, L.; Chu, C.J.

    1999-07-01

    Many studies have indicated that the threat from toxic air pollutants such as VOCs comes not through inhalation by humans while the pollutants are in a gaseous state but through absorption when the pollutants are in a solid state such as in an aerosol or particulate form. Pollutants such as Polycyclic Aromatic Hydrocarbons (PAHs) usually exist in a semi-volatile state. To assess the risk of the PAHs, one needs to estimate the dose of the pollutants to which a human would be exposed through various pathways. In this study, the authors modified a Spatial Multimedia Compartmental Model (SMCM) originally developed by UCLA Professor Cohen to predict the PAHs distribution among multimedia such as air, water, soil and sediment in the Taipei metropolitan area. Three PAHs were considered in this study. They are Benzo(a)pyrene, Pyrene and Chrysene. When PAHs are emitted into atmosphere, physical and chemical mechanisms may redistribute the PAHs among multimedia. Five cases of PAHs distribution in multimedia were simulated: (1) PAHs distribution in a dry condition, (2) PAHs distribution when there are different dry deposition velocities, (3) PAHs distribution under a single rainfall event, (4) PAHs distribution when there are different soil properties, (5) PAHs distribution under a random rainfall case. The simulation results are concluded: (1) In the dry case, the PAHs accumulate mostly in soil and air compartments, (2) Different dry depositing velocities will affect the PAHs distribution among compartments. (3) Different soil properties affect the PAHs concentration in the soil and sediment compartments, (4) The soil PAHs concentrations usually increase for those PAHs with a high solid/gas ratio. (5) The random rainfall only affects the PAHs concentration in the soil.

  6. Dry deposition of polycyclic aromatic hydrocarbons in ambient air

    SciTech Connect

    Sheu, H.L.; Lee, W.J.; Su, C.C.; Chao, H.R.; Fan, Y.C.

    1996-12-01

    Dry deposition and air sampling were undertaken, simultaneously, in the ambient air of an urban site and a petrochemical-industry (PCI) plant by using several dry deposition plates and PS-1 samplers from January to May 1994 in southern Taiwan. The dry deposition plate with a smooth surface was always pointed into the wind. Twenty-one polycyclic aromatic hydrocarbons (PAHs) were analyzed by a gas chromatography/mass spectrometer (GC/MSD). The dry deposition flux of total-PAHs in urban and PCI sites averaged 166 and 211 {micro}g/m{sup 2}{center_dot}d, respectively. In general, the PAH dry deposition flux increased with increases in the PAH concentration in the ambient air. The PAH pattern of dry deposition flux in both urban and PCI sites were similar to the pattern measured by the filter of the PS-1 sampler and completely different from the PAH pattern in the gas phase. The higher molecular weight PAHs have higher dry deposition velocities. This is due to the fact that higher molecular weight PAHs primarily associated with the particle phase are deposited mostly by gravitational settling, while the gas phase PAHs were between 0.001 and 0.010 cm/s, only the lower molecular-weight PAHs--Nap and AcPy--had a significant fraction of dry deposition flux contributed by the gas phase. All the remaining higher molecular-weight PAHs had more than 94.5% of their dry deposition flux resulting from the particle phase. This is due to the fact that higher molecular weight PAHs have a greater fraction in the particle phase and the dry deposition velocities of particulates are much higher than those of the gas phase.

  7. Dissociation of polycyclic aromatic hydrocarbons: molecular dynamics studies

    NASA Astrophysics Data System (ADS)

    Simon, A.; Rapacioli, M.; Rouaut, G.; Trinquier, G.; Gadéa, F. X.

    2017-03-01

    We present dynamical studies of the dissociation of polycyclic aromatic hydrocarbon (PAH) radical cations in their ground electronic states with significant internal energy. Molecular dynamics simulations are performed, the electronic structure being described on-the-fly at the self-consistent-charge density functional-based tight binding (SCC-DFTB) level of theory. The SCC-DFTB approach is first benchmarked against DFT results. Extensive simulations are achieved for naphthalene , pyrene and coronene at several energies. Such studies enable one to derive significant trends on branching ratios, kinetics, structures and hints on the formation mechanism of the ejected neutral fragments. In particular, dependence of branching ratios on PAH size and energy were retrieved. The losses of H and C2H2 (recognized as the ethyne molecule) were identified as major dissociation channels. The H/C2H2 ratio was found to increase with PAH size and to decrease with energy. For , which is the most interesting PAH from the astrophysical point of view, the loss of H was found as the quasi-only channel for an internal energy of 30 eV. Overall, in line with experimental trends, decreasing the internal energy or increasing the PAH size will favour the hydrogen loss channels with respect to carbonaceous fragments. This article is part of the themed issue 'Theoretical and computational studies of non-equilibrium and non-statistical dynamics in the gas phase, in the condensed phase and at interfaces'.

  8. Estimation of Chronic Personal Exposure to Airborne Polycyclic Aromatic Hydrocarbons

    PubMed Central

    Choi, Hyunok; Zdeb, Michael; Perera, Frederica; Spengler, John

    2015-01-01

    Background Polycyclic aromatic hydrocarbons (PAH) exposure from solid fuel burning represents an important public health issue for the majority of the global population. Yet, understanding of individual-level exposures remains limited. Objectives To develop regionally adaptable chronic personal exposure model to pro-carcinogenic PAH (c-PAH) for the population in Kraków, Poland. Methods We checked the assumption of spatial uniformity in eight c-PAH using the coefficients of divergence (COD), a marker of absolute concentration differences. Upon successful validation, we developed personal exposure models for eight pro-carcinogenic PAH by integrating individual-level data with area-level meteorological or pollutant data. We checked the resulting model for accuracy and precision against home outdoor monitoring data. Results During winter, COD of 0.1 for Kraków suggest overall spatial uniformity in the ambient concentration of the eight c-PAH. The three models that we developed were associated with index of agreement approximately equal to 0.9, root mean square error < 2.6 ng/m3, and 90th percentile of absolute difference ≤ 4 ng/m3 for the predicted and the observed concentrations for eight pro-carcinogenic PAH. Conclusions Inexpensive and logistically feasible information could be used to estimate chronic personal exposure to PAH profiles, in lieu of costly and labor-intensive personal air monitoring at wide scale. At the same time, thorough validation through direct personal monitoring and assumption checking are critical for successful model development. PMID:25965038

  9. Photolysis of polycyclic aromatic hydrocarbons adsorbed on fly ash

    SciTech Connect

    Behymer, T.D.

    1987-01-01

    Polycyclic aromatic hydrocarbons (PAH) are formed by the combustion of almost any fuel under oxygen-deficient conditions. Previous laboratory studies have found that many PAH degrade with lifetimes as short as a few hours; however, studies of marine and lacustrine sediments, the ultimate sinks of PAH, have shown relative abundances of PAH which are similar to those in combustion sources; this suggests that PAH are stable in the atmosphere. Eighteen PAH adsorbed on carbon black and fifteen coal fly ashes of varying physical and chemical composition were photolyzed in order to study their atmospheric fate. Photolytic half-lives for these particle-bound PAH were found to be highly dependent on the substrate onto which they were adsorbed. On low-carbon fly ash, PAH showed a wide range of half-lives, indicating a relationship between PAH structure and photochemical reactivity. However, PAH on carbon black and fly ashes with a high-carbon content, show similar half-lives for most PAH including reactive PAH such as anthracene and benzo(a)pyrene. This indicates a photolytic process that is independent of structure and dependent on the physical and chemical nature of the fly ash. Surprisingly, no other parameter accounts for observed PAH reactivity. Substrate characteristics such as surface area, porosity, particle size, surface pH, and iron content have all been suggested to influence the rate of PAH degradation. However, these parameters, measured for substrates studied in this thesis, do not correlate with PAH reactivity. Because carbon black and high-carbon fly ashes stabilize reactive PAH, it is these substrates which would facilitate the transport of PAH from combustion sources through the atmosphere to ultimate sinks.

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

    SciTech Connect

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

    2007-04-01

    High temperature carbon oxidation in primary aluminum smelters results in the release of polycyclic aromatic hydrocarbons (PAH) into the environment. The main source of PAH are the anodes, which are composed of petroleum coke (black carbon, BC) and coal tar pitch. To elucidate the dominant carbonaceous phase controlling the environmental fate of PAH in aluminum smelter residues (coke BC and/or coal tar), the sorptive behavior of PAHs has been determined, using passive samplers and infinite-sink desorption methods. Samples directly from the wet scrubber were studied as well as ones from an adjacent 20-year old storage lagoon and roof dust from the smelter. Carbon-normalized distribution coefficients of native PAHs were 2 orders of magnitude higher than expected based on amorphous organic carbon (AOC)/water partitioning, which is in the same order of magnitude as reported literature values for soots and charcoals. Sorption isotherms of laboratory-spiked deuterated phenanthrene showed strong (about 100 times stronger than AOC) but nonetheless linear sorption in both fresh and aged aluminum smelter residues. The absence of nonlinear behavior typical for adsorption to BC indicates that PAH sorption in aluminum smelter residues is dominated by absorption into the semi-solid coal tar pitch matrix. Desorption experiments using Tenax showed that fresh smelter residues had a relatively large rapidly desorbing fraction of PAH (35-50%), whereas this fraction was strongly reduced (11-16%) in the lagoon and roof dust material. Weathering of the coal tar residue and/or redistribution of PAH between coal tar and BC phases could explain the reduced availability in aged samples. 38 refs., 5 figs., 1 tab.

  11. From Interstellar Polycyclic Aromatic Hydrocarbons and Ice to the Origin of Life

    NASA Technical Reports Server (NTRS)

    Allamandola, Louis

    2004-01-01

    Tremendous strides have been made in our understanding of interstellar material over the past twenty years thanks to significant, parallel developments in observational astronomy and laboratory astrophysics. Twenty years ago the composition of interstellar dust was largely guessed at, the concept of ices in dense molecular clouds ignored, and the notion of large, abundant, gas phase, carbon rich molecules widespread throughout the interstellar medium (ISM) considered impossible. Today the composition of dust in the diffuse ISM is reasonably well constrained to cold refractory materials comprised of amorphous and crystalline silicates mixed with an amorphous carbonaceous material containing aromatic structural units and short, branched aliphatic chains. In the dense ISM, the birthplace of stars and planets, these cold dust particles are coated with mixed molecular ices whose composition is very well constrained. Lastly, the signature of carbon-rich polycyclic aromatic hydrocarbons (PAHs), shockingly large molecules by early interstellar chemistry standards, is widespread throughout the Universe. The first part of this talk will describe how infrared studies of interstellar space, combined with laboratory simulations, have revealed the composition of interstellar ices (the building blocks of comets) and the high abundance and nature of interstellar PAHs. The laboratory database has now enabled us to gain insight into the identities, abundances, and physical state of many interstellar materials. Within a dense molecular cloud, and especially in the presolar nebula, the materials frozen into the interstellar/precometary ices are photoprocessed by ultraviolet light and produce more complex molecules. The remainder of the presentation will focus on the photochemical evolution of these materials and the possible role of these compounds on the to the carbonaceous components of micrometeorites, they are likely to have been important sources of complex materials on the early

  12. Polycyclic aromatic hydrocarbons profiles of spent drilling fluids deposited at Emu-Uno, Delta State, Nigeria.

    PubMed

    Iwegbue, Chukwujindu M A

    2011-10-01

    The concentrations and profiles of polycyclic aromatic hydrocarbons were determined in spent drilling fluid deposited at Emu-Uno, Delta State of Nigeria. The total concentrations of polycyclic aromatic hydrocarbons in the spent drilling fluid deposits ranged between 40 and 770 μg kg(-1). The PAHs profile were predominantly 2- and 3-rings with acenaphthalene, phenanthrene, fluorene being the predominant PAHs. The prevalence of 2- and 3-rings PAHs in the spent drilling fluid deposits indicate contamination of the drilling fluids with crude oil during drilling. Incorporation of spent drilling fluids into the soil has serious implication for soil, surface water and groundwater quality.

  13. Remediation of polycyclic aromatic hydrocarbons. (Latest citations from Pollution abstracts). Published Search

    SciTech Connect

    1995-10-01

    The bibliography contains citations concerning the removal of polycyclic aromatic hydrocarbons from contaminated soil or water. The chemical or biological processes that destroy these contaminants or reduce their toxicity are discussed. Techniques include treatments used in above-ground reactors or in situ detoxification of contaminated sites. The citations examine the relationship between the chemical structure of polycyclic aromatic hydrocarbons and rate of decomposition; selection of the most effective microorganisms for biological degradation; and factors which can accelerate or inhibit degradation.(Contains 50-250 citations and includes a subject term index and title list.) (Copyright NERAC, Inc. 1995)

  14. Remediation of polycyclic aromatic hydrocarbons. (Latest citations from Pollution Abstracts). Published Search

    SciTech Connect

    1995-03-01

    The bibliography contains citations concerning the removal of polycyclic aromatic hydrocarbons from contaminated soil or water. The chemical or biological processes that destroy these contaminants or reduce their toxicity are discussed. Techniques include treatments used in above-ground reactors or in situ detoxification of contaminated sites. The citations examine the relationship between the chemical structure of polycyclic aromatic hydrocarbons and rate of decomposition; selection of the most effective microorganisms for biological degradation; and factors which can accelerate or inhibit degradation. (Contains a minimum of 108 citations and includes a subject term index and title list.)

  15. Remediation of polycyclic aromatic hydrocarbons. (Latest citations from Pollution Abstracts). Published Search

    SciTech Connect

    1996-12-01

    The bibliography contains citations concerning the removal of polycyclic aromatic hydrocarbons from contaminated soil or water. The chemical or biological processes that destroy these contaminants or reduce their toxicity are discussed. Techniques include treatments used in above-ground reactors or in situ detoxification of contaminated sites. The citations examine the relationship between the chemical structure of polycyclic aromatic hydrocarbons and rate of decomposition; selection of the most effective microorganisms for biological degradation; and factors which can accelerate or inhibit degradation.(Contains 50-250 citations and includes a subject term index and title list.) (Copyright NERAC, Inc. 1995)

  16. Remediation of polycyclic aromatic hydrocarbons. (Ltest citations from Pollution abstracts). Published Search

    SciTech Connect

    Not Available

    1994-07-01

    The bibliography contains citations concerning the removal of polycyclic aromatic hydrocarbons from contaminated soil or water. The chemical or biological processes that destroy these contaminants or reduce their toxicity are discussed. Techniques include treatments used in above-ground reactors or in situ detoxification of contaminated sites. The citations examine the relationship between the chemical structure of polycyclic aromatic hydrocarbons and rate of decomposition; selection of the most effective microorganisms for biological degradation; and factors which can accelerate or inhibit degradation. (Contains a minimum of 82 citations and includes a subject term index and title list.)

  17. Remediation of polycyclic aromatic hydrocarbons. (Latest citations from Pollution abstracts). Published Search

    SciTech Connect

    1997-12-01

    The bibliography contains citations concerning the removal of polycyclic aromatic hydrocarbons from contaminated soil or water. The chemical or biological processes that destroy these contaminants or reduce their toxicity are discussed. Techniques include treatments used in above-ground reactors or in situ detoxification of contaminated sites. The citations examine the relationship between the chemical structure of polycyclic aromatic hydrocarbons and rate of decomposition; selection of the most effective microorganisms for biological degradation; and factors which can accelerate or inhibit degradation.(Contains 50-250 citations and includes a subject term index and title list.) (Copyright NERAC, Inc. 1995)

  18. Source apportionment of polycyclic aromatic hydrocarbons in surface sediment of mud areas in the East China Sea using diagnostic ratios and factor analysis.

    PubMed

    Deng, Wei; Li, Xian Guo; Li, Sheng Yong; Ma, Yan Yan; Zhang, Da Hai

    2013-05-15

    Polycyclic aromatic hydrocarbons (PAHs) and aliphatic hydrocarbons (AHs) have been quantified for surface sediments collected from the East China Sea (ECS). Our results showed that relatively high levels of PAHs and AHs occurred in both the inner and outer mud areas, while their concentrations at the control site were much lower. AHs for all samples were dominated by the unresolved complex mixture (UCM). Results from diagnostic ratios revealed that sedimentary PAHs were mainly originated from mixed combustion residues of biomass, coal, and petroleum. Combustion residues of petroleum and oil were responsible for the presence of high AHs concentrations. We also conducted factor analysis (FA) to further characterize the PAH and AH sources. Four factors were identified based on the loading of components and attributed to coal and wood combustion (Factor 1), traffic-related sources (Factor 2), petrogenic source (Factor 3) and natural gas combustion (Factor 4).

  19. Fate of polycyclic aromatic hydrocarbons during composting of oily sludge.

    PubMed

    Kriipsalu, M; Marques, M; Hogland, W; Nammari, D R

    2008-01-01

    In order to assess the effectiveness of aerobic degradation with emphasis on the 16 U.S. EPA priority polycyclic aromatic hydrocarbons (PAH), oily sludge generated by a dissolved air flotation flocculation unit of a wastewater treatment plant in a petroleum refinery was amended with remediated oil-contaminated soil and non-mature garden waste compost 40:40:20 (wet weight) respectively. About 21 t of the mixture with a top-layer formed by 30 cm of remediated soil was treated in a 28 m3 air-forced reactor. The PAH concentration was monitored for 370 days. In the top-layer, a reduction of 88 % of the total extractable PAH was measured at day 62 and a final reduction of 93% at day 370. In the mixture, a reduction of 72% in total PAH was measured at day 62, followed by fluctuation in concentration with a final measured reduction of 53% at day 370. The analysis of individual PAH in the mixture suggested that volatilization and biodegradation are the main mechanisms responsible for the reduction of 2 ring PAH and 3-4 ring PAH, respectively. Fluctuation of 5-6 ring PAH concentrations with increase observed at the end of the period might result from a combination of the following: (i) sequestration of large PAH in the organic matrix (reducing bioavailability, biodegradability and eventually, extractability) and desorption as composting progresses; (ii) heterogeneous distribution of the stable large PAH in the mixture, thus affecting sampling. It was concluded that one-time composting in static-aerated biopiles with organic amendments as the sole strategy to treat oily sludge is very effective in reducing the content of 2-4 ring PAH, but it is not effective in reducing the content of 5-6 ring PAHs, even after a relatively long time span (370 d). The concentrations measured in the remediated soil that formed the top layer after 62 days of composting suggests that further relevant reduction of residual PAH (89% of total PAH and 69% of 5-6 ring PAH) can be obtained if the

  20. The environmental fate of polycyclic aromatic hydrocarbons associated with particles

    NASA Astrophysics Data System (ADS)

    Kim, Daekyun

    This study focused on the transport and distribution in the environment, the phototransformation, and the source identification of particle-associated polycyclic aromatic hydrocarbons (PAHs). To investigate the main inputs and sources of PAHs, particulate, dissolved, and colloid-bound PAHs in stream and precipitation samples collected along an urban tributary were monitored between October 2004 and March 2005. Particulate matter carried by stormwater runoff was the major source of PAHs in surface water in the early rainy season. Indirect deposition of PAHs into surface water is likely a more significant input pathway for total PAHs than direct dry or wet deposition during the wet season. Selected PAH ratios indicate that observed PAHs in rainwater came from pyrogenic sources and those in surface water had more complicated and variable origins. To examine possible changes in the PAH profiles caused by environmental aging, soot particles were exposed to simulated sunlight and disappearance rates of PAHs were determined. An obvious two-phase disappearance was observed for naphthalene, acenaphthylene, acenaphthene, and fluorene, while phenanthrene and anthracene exhibited this behavior for all but the highest soot loading. The first phase loss occurred within 3-10 hours is 5-40 times faster than the second phase loss. Only single mode of disappearance, however, was observed for the higher molecular weight PAHs with 4-6 rings. Sources of PAHs from surface waters and sediments should be determined by considering the potential influence of aging on any diagnostic method. Due to differences in disappearance rates of individual PAHs, prolonged exposure to sunlight could change the interpretation of characteristic PAH ratios. The apparent disappearance rates of PAHs on soot are governed by photodegradation and diffusion kinetics. The effective diffusion coefficients, the photodegradation rate constants, and the light penetration depth for fluorene, phenanthrene, and

  1. Polycyclic aromatic hydrocarbons in US and Swedish smokeless tobacco products

    PubMed Central

    2013-01-01

    Background Debate about the health implications of using smokeless tobacco products (STPs) has prompted considerable interest in characterising their levels of toxic and carcinogenic components. In the present study seventy smokeless tobacco products from the US and Sweden, categorized as chewing tobacco, dry and moist snuff, hard and soft pellets, plug, and loose and portion snus, were analysed for twenty one polycyclic aromatic hydrocarbons (PAHs). The tested brands represented 80-90% of the 2008 market share for the major STP categories in these two countries. Results There were significant differences in the total and individual PAH concentrations in the different styles of product. Substantially higher levels of total PAHs (10–60 fold) were found in moist and dry snuff and soft pellets than in the other smokeless tobacco styles. The individual PAH concentrations followed the same patterns as total PAHs except for naphthalene, for which the highest concentrations were found in snus and moist snuff. Good correlations were obtained between benzo[a]pyrene (B[a]P) and all the other PAHs except naphthalene, 1-methylnaphthalene and 2-methylnaphthalene, providing evidence for the first time that it can be used as a good marker for PAHs in STPs. Results were generally in good agreement with two previous studies of PAHs in STPs, except for naphthalene for which significantly lower concentrations were found than previously reported. Analysis of the ratios of different PAHs confirmed that the use of fire-cured tobaccos in the snuffs and soft pellet were the major source of PAHs in these product styles, and provided, for the first time, some indications as to the source of PAHs in the other STP styles, including petrogenic and other combustion sources. Conclusions This study confirms the presence of PAHs in STPs, and identifies substantial differences between the levels in different STP categories. Since previous studies of naphthalene concentrations in STPs differed so

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

    NASA Technical Reports Server (NTRS)

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

    1994-01-01

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

  3. Ecotoxicity of a polycyclic aromatic hydrocarbon (PAH)-contaminated soil.

    PubMed

    Eom, I C; Rast, C; Veber, A M; Vasseur, P

    2007-06-01

    Soil samples from a former cokery site polluted with polycyclic aromatic hydrocarbons (PAHs) were assessed for their toxicity to terrestrial and aquatic organisms and for their mutagenicity. The total concentration of the 16 PAHs listed as priority pollutants by the US Environmental Protection Agency (US-EPA) was 2634+/-241 mg/kgdw in soil samples. The toxicity of water-extractable pollutants from the contaminated soil samples was evaluated using acute (Vibrio fischeri; Microtox test, Daphnia magna) and chronic (Pseudokirchneriella subcapitata, Ceriodaphnia dubia) bioassays and the EC values were expressed as percentage water extract in the test media (v/v). Algal growth (EC50-3d=2.4+/-0.2% of the water extracts) and reproduction of C. dubia (EC50-7d=4.3+/-0.6%) were the most severely affected, compared to bacterial luminescence (EC50-30 min=12+/-3%) and daphnid viability (EC50-48 h=30+/-3%). The Ames and Mutatox tests indicated mutagenicity of water extracts, while no response was found with the umu test. The toxicity of the soil samples was assessed on the survival and reproduction of earthworms (Eisenia fetida) and collembolae (Folsomia candida), and on the germination and growth of higher plants (Lactuca sativa L.: lettuce and Brassica chinensis J.: Chinese cabbage). The EC50 values were expressed as percentage contaminated soil in ISO soil test medium (weight per weight-w/w) and indicated severe effects on reproduction of the collembola F. candida (EC50-28 d=5.7%) and the earthworm E. fetida (EC50-28 d=18% and EC50-56 d=8%, based on cocoon and juvenile production, respectively). Survival of collembolae was already affected at a low concentration of the contaminated soil (EC50-28 d=11%). The viability of juvenile earthworms was inhibited at much lower concentrations of the cokery soil (EC50-14 d=28%) than the viability of adults (EC50-14 d=74%). Only plant growth was inhibited (EC50-17d=26%) while germination was not. Chemical analyses of water extracts allowed

  4. Radiation and chemical studies of carcinogens, polycyclic aromatic hydrocarbons

    SciTech Connect

    Chen, Chiachieh.

    1989-01-01

    Radiation and polycyclic aromatic hydrocarbons (PAH's) are environmental pollutants. 3MC effectively neutralized the lethality of C3H mouse 10T1/2 cells resulting from B(a)P or DMBA. PAH binding to macromolecules increased linearly with exposure, but DNA-adducts saturated with exposure. 3MC or {alpha}NF appreciably reduced the formation of DNA adducts due to B(a)P or DMBA. The reductions in DNA-adduct formation did not result from a reduction in the induction of AHH. By using DNA adducts as chemical dose, and plotting the DMBA survival curve as a function of DMBA-DNA adducts, the curve was an exponential curve. A similar application with B(a)P-DNA adduct showed the survival curve as a shoulder followed by an exponential region. When 10T1/2 cells were treated with X-radiation and a PAH, the nontoxic compounds and B(a)P did not show any significant effect on X-ray survival curve. However, the damage due to DMBA was found to be additive to X-ray damage. The latter property of DMBA was lost when cells were cotreated with 3MC and DMBA presumably because damage to DNA due to DMBA alone was suppressed. Thus, the combined action is complex. DMBA produced damage in 10T1/2 cells that added to radiation damage. Although a nontoxic PAH could neutralize the effect of a toxic PAH, the former were not able to mitigate the lethal effects of radiation. Operationally, the latter results suggested that a nontoxic PAH could cancel out the effect of a toxic one because it inhibited the formation of the DNA damage with which radiation damage could interact rather than because the nontoxic PAH removed the radiation damage with which the PAH could interact. It showed that at least 4 hours were required for DMBA to affect the sublethal radiation damage repair, a period long enough for a large fraction of the latter damage to have been lost.

  5. New biomarkers of occupational exposure to polycyclic aromatic hydrocarbons.

    PubMed

    Seidel, Albrecht; Spickenheuer, Anne; Straif, Kurt; Rihs, Hans-Peter; Marczynski, Boleslaw; Scherenberg, Michael; Dettbarn, Gerhard; Angerer, Jürgen; Wilhelm, Michael; Brüning, Thomas; Jacob, Jürgen; Pesch, Beate

    2008-01-01

    Polycyclic aromatic hydrocarbons (PAH) are metabolized in a complex manner. Although biological activity is associated with diol-epoxide formation, phenolic metabolites have predominantly been used in human biomonitoring. In this study monohydroxylated and new metabolites were characterized as biomarkers for occupational PAH exposure. In 97 male workers, personal exposure to 16 airborne PAH compounds was measured during shift. In postshift urine, 1-hydroxypyrene and 1,6- and 1,8-dihydroxypyrene (1-OHP, DiOHP) were determined as metabolites of pyrene (P), and the sum of 1-, 2-, 3-, 4-, and 9-hydroxyphenanthrenes (OHPHE), and PHE-dihydrodiols (PHED) as metabolites of phenanthrene (PHE). The referent group comprised 21 nonsmoking construction workers. Median (interquartile range) shift concentrations of airborne P and PHE were 1.46 (0.62-4.05 microg/m(3)) and 10.9 (3.69-23.77 microg/m(3)), respectively. The corresponding parameters were 3.86 (2.08-7.44) microg/g creatinine (crn) for 1-OHP, 0.66 (0.17-1.65) microg/g crn for DiOHP, 11.44 (5.21-34.76) microg/g crn for OHPHE, and 12.28 (3.3-97.76) microg/g crn for PHED in PAH-exposed workers. The median levels of 1-OHP and OHPHE were 0.09 (0.08-0.17 microg/m(3)) and 0.59 (0.45-1.39 microg/m(3)), respectively, in the referents. PHE correlated significantly with OHPHE and PHED, and P with 1-OHP but not with DiOHP. Under a doubling of PHE, OHPHE increased by a factor of 1.56 and PHED by 1.57. With a doubling of P, 1-OHP rose by 1.31 and DiOHP by 1.27. P is predominantly metabolized into 1-OHP, whereas PHE is metabolized equally into OHPHE and PHED. Thus metabolites of PHE were found as reliable biomarkers for PAH exposure.

  6. An Emission Inventory of Polycyclic Aromatic Hydrocarbons in China

    NASA Astrophysics Data System (ADS)

    Mu, Xilong; Zhu, Xianlei; Wang, Xuesong

    2015-04-01

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

  7. Determination of polycyclic aromatic hydrocarbons in dry tea

    PubMed Central

    ADISA, AFOLABI; JIMENEZ, ANGELICA; WOODHAM, CARA; ANTHONY, KEVIN; NGUYEN, THAO; SALEH, MAHMOUD A.

    2016-01-01

    Twenty-eight different tea samples sold in the United States were evaluated using high-performance liquid chromatography (HPLC) with fluorescence detection (FLD) for their contamination with polycyclic aromatic hydrocarbons (PAHs). Many PAHs exhibit carcinogenic, mutagenic, and teratogenic properties and have been related to several kinds of cancer in man and experimental animals. The presence of PAHs in environmental samples such as water, sediments, and particulate air has been extensively studied, but food samples have received little attention. Eighteen PAHs congeners were analyzed, with percentage recovery higher than 85%. Contamination expressed as the sum of the 18 analyzed PAHs was between 101 and 1337 μg/kg on dry mass and the average contents in all of the 28 examined samples was 300 μg/kg on dry mass. Seven of the congeners were found in all samples with wide ranges of concentrations as follows: fluorene (7–48 μg/kg), anthracene (1–31 μg/kg), pyrene (1–970 μg/kg), benzo(a)anthracene (1–18 μg/kg) chrysene (17–365 μg/kg), benzo(a)pyrene (1–29 μg/kg), and indeno(1,2,3-cd)pyrene (4–119 μg/kg). The two most toxic congeners benzo(a)pyrene and dibenzo(a,h)anthracene were found at high concentrations only in Earl Grey Twinnings, Earl Grey Harney& Sons Fine Teas, and Chai Ultra Spice Black Tea Twinnings. Six PAH congeners are considered as suspected carcinogens (U.S.EPA), formed the basis of the estimation of the toxic equivalent (TEQ), Chai Ultra-Spice Black Tea Twinnings had the highest TEQ (110.9) followed by two grey tea samples, Earl Grey Harney & Sons Fine Tea (57.7) and Earl Grey Twinnings (54.5). Decaffeinated grey teas had the lowest TEQs, decaffeinated Earl Grey Bigelow (9.4) and Green Tea Honey Lemon Decaffeinated Lipton (9.6). PMID:26065515

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

    NASA Astrophysics Data System (ADS)

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

    2014-12-01

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

  9. Carbon isotope systematics of individual hydrocarbons in hydrothermal petroleum from Escanaba Trough, northeastern Pacific Ocean.

    PubMed

    Simoneit, B R; Schoell, M; Kvenvolden, K A

    1997-01-01

    We submitted individual aliphatic and polycyclic aromatic hydrocarbons in samples of hydrothermal petroleum from Escanaba Trough to compound specific isotope analysis to trace their origins. The carbon isotope compositions of the alkanes and polycyclic aromatic hydrocarbons (means -27.5 and -24.7%, respectively) reflect a primarily terrestrial organic matter source.

  10. Polycyclic aromatic hydrocarbons in Australian coals. III. Structural elucidation by proton nuclear magnetic resonance spectroscopy

    SciTech Connect

    Chaffee, A.L.; Fookes, C.J.R.

    1988-01-01

    The molecular structures of a number of tetra- and pentacyclic aromatic hydrocarbons present in extracts of Victorian brown coal have been unambiguously established by /sup 1/H-NMR. The determined structures support the hypothesis that these polycyclic aromatic hydrocarbons (PAHs) are diagenetically derived from triterpenoid precursors based on the oleanane, ursane and lupane skeletons. The occurrence of diastereoisomerism in these PAHs has been revealed for the first time and the diastereomeric configurations of one pair of triaromatic compounds (XI and XII) defined.

  11. Recent analytical methods for atmospheric polycyclic aromatic hydrocarbons and their derivatives.

    PubMed

    Hayakawa, Kazuichi; Tang, Ning; Toriba, Akira

    2017-01-01

    Polycyclic aromatic hydrocarbons (PAHs) and nitropolycyclic aromatic hydrocarbons (NPAHs) are ubiquitous environmental pollutants. Moreover, some oxidative metabolites of these pollutants, such as hydroxylated and epoxide PAHs, cause endocrine disruption or produce reactive oxygen species. These compounds have become a large concern from the viewpoint of particulate matter (PM2.5 ) pollution. This report deals with recent studies concerning analytical methods for PAHs, NPAHs and related compounds in atmospheric and biological samples.

  12. Biosurfactant production by a soil Pseudomonas strain growing on polycyclic aromatic hydrocarbons

    SciTech Connect

    Deziel, E.; Paquette, G.; Villemur, R.; Lepine, F.

    1996-06-01

    Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous pollutants occurring mostly as a result of fossil fuel combustion and as by-products of industrial activities. The bioremediation of soils contaminated with PAHs is limited by the poor availability of dyrophobic contaminants to microorganisms. Surfactants can help. Recent studies indicate that addition of surfactants can enhance hydrocarbon biodegradation. This study examines whether production of surfactants by PAH-metabolizing microorganisms is part of their strategy for growing on such poorly available substrates.

  13. The possible existence of interstellar Polycyclic Aromatic Hydrocarbons (PAHs) in collected interplanetary dust particles

    NASA Technical Reports Server (NTRS)

    Sandford, S. A.

    1986-01-01

    Extraterrestrial dust particles which are 3 to 50 microns in size are routinely collected in the stratosphere and are now available for general laboratory study. These grains represent true Interplanetary Dust Particles (IDPs). Issues associated with the carbon containing components of IDPs which occur in a variety of physical forms, including amorphous mantles and matrix materials, are addressed. The observed properties of the hydrocarbon phase in IDPs are compared with those expected for polycyclic aromatic hydrocarbons (PAHs).

  14. The Abundances of Hydrocarbon Functional Groups in the Interstellar Medium Inferred from Laboratory Spectra of Hydrogenated and Methylated Polycyclic Aromatic Hydrocarbons

    NASA Astrophysics Data System (ADS)

    Steglich, M.; Jäger, C.; Huisken, F.; Friedrich, M.; Plass, W.; Räder, H.-J.; Müllen, K.; Henning, Th.

    2013-10-01

    Infrared (IR) absorption spectra of individual polycyclic aromatic hydrocarbons (PAHs) containing methyl (\\sbondCH3), methylene (\\protect{\\epsfbox{art/apjs484229un01.eps}}CH2), or diamond-like \\protect{\\epsfbox{art/apjs484229un02.eps}}CH groups and IR spectra of mixtures of methylated and hydrogenated PAHs prepared by gas-phase condensation were measured at room temperature (as grains in pellets) and at low temperature (isolated in Ne matrices). In addition, the PAH blends were subjected to an in-depth molecular structure analysis by means of high-performance liquid chromatography, nuclear magnetic resonance spectroscopy, and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Supported by calculations at the density functional theory level, the laboratory results were applied to analyze in detail the aliphatic absorption complex of the diffuse interstellar medium at 3.4 μm and to determine the abundances of hydrocarbon functional groups. Assuming that the PAHs are mainly locked in grains, aliphatic CH x groups (x = 1, 2, 3) would contribute approximately in equal quantities to the 3.4 μm feature (N CHx /N H ≈ 10-5-2 × 10-5). The abundances, however, may be two to four times lower if a major contribution to the 3.4 μm feature comes from molecules in the gas phase. Aromatic \\epsfbox{art/apjs484229un03.eps} CH groups seem to be almost absent from some lines of sight, but can be nearly as abundant as each of the aliphatic components in other directions (N_{\\epsfbox{art/apjs484229un03.eps} CH}/N H lsim 2 × 10-5 upper value for grains). Due to comparatively low binding energies, astronomical IR emission sources do not display such heavy excess hydrogenation. At best, especially in protoplanetary nebulae, \\protect{\\epsfbox{art/apjs484229un01.eps}}CH2 groups bound to aromatic molecules, i.e., excess hydrogens on the molecular periphery only, can survive the presence of a nearby star.

  15. New SERS Substrates For Polycyclic Aromatic Hydrocarbon (PAH) Detection: Towards Quantitative SERS Sensors For Environmental Analysis

    SciTech Connect

    Peron, O.; Rinnert, E.; Compere, C.; Toury, T.; Lamy de la Chapelle, M.

    2010-08-06

    In the investigation of chemical pollutions, such as PAHs (Polycyclic Aromatic Hydrocarbons) at low concentration in aqueous medium, surface-enhanced Raman scattering (SERS) stands for an alternative to the inherent low cross-section of normal Raman scattering. Indeed, SERS is a very sensitive spectroscopic technique due to the excitation of the surface plasmon modes of the nanostructured metallic film.

  16. Toxicity of aromatic polycyclic hydrocarbons. (Latest citations from the Life Sciences Collection database). Published Search

    SciTech Connect

    Not Available

    1994-11-01

    The bibliography contains citations concerning the toxicity and biochemical effects of aromatic polycyclic hydrocarbons. Topics include effects on metabolism and liver activity, cellular responses, binding characteristics, and the occurrence and path of the compounds in food chains. Bioaccumulation studies in specific areas, and isolation and detection techniques are also considered. (Contains 250 citations and includes a subject term index and title list.)

  17. Toxicity of aromatic polycyclic hydrocarbons. (Latest citations from the Life Sciences Collection database). Published Search

    SciTech Connect

    Not Available

    1993-11-01

    The bibliography contains citations concerning the toxicity and biochemical effects of aromatic polycyclic hydrocarbons. Topics include effects on metabolism and liver activity, cellular responses, binding characteristics, and the occurrence and path of the compounds in food chains. Bioaccumulation studies in specific areas, and isolation and detection techniques are also considered. (Contains 250 citations and includes a subject term index and title list.)

  18. Removal of crude oil polycyclic aromatic hydrocarbons via organoclay-microbe-oil interactions.

    PubMed

    Ugochukwu, Uzochukwu C; Fialips, Claire I

    2017-05-01

    Clay minerals are quite vital in biogeochemical processes but the effect of organo-clays in the microbial degradation of crude oil polycyclic aromatic hydrocarbons is not well understood. The role of organo-saponite and organo-montmorillonite in comparison with the unmodified clays in crude oil polycyclic aromatic hydrocarbons (PAHs) removal via adsorption and biodegradation was studied by carrying out microcosm experiments in aqueous clay/oil systems with a hydrocarbon degrading microbial community that is predominantly alcanivorax spp. Montmorillonite and saponite samples were treated with didecyldimethylammonium bromide to produce organo-montmorillonite and organo-saponite used in this study. Obtained results indicate that clays with high cation exchange capacity (CEC) such as montmorillonite produced organo-clay (organomontmorillonite) that was not stimulatory to biodegradation of crude oil polycyclic aromatic compounds, especially the low molecular weight (LMW) ones, such as dimethylnaphthalenes. It is suggested that interaction between the organic phase of the organo-clay and the crude oil PAHs which is hydrophobic in nature must have reduced the availability of the polycyclic aromatic hydrocarbons for biodegradation. Organo-saponite did not enhance the microbial degradation of dimethylnaphthalenes but enhanced the biodegradation of some other PAHs such as phenanthrene. The unmodified montmorillonite enhanced the microbial degradation of the PAHs and is most likely to have done so as a result of its high surface area that allows the accumulation of microbes and nutrients enhancing their contact.

  19. Sources and deposition of polycyclic aromatic hydrocarbons to western US national parks

    EPA Science Inventory

    Seasonal snowpack, lichens, and lake sediment cores were collected from fourteen lake catchments in eight western U.S. National Parks and analyzed for sixteen polycyclic aromatic hydrocarbons (PAHs) to determine their current and historical deposition, as well as to identify thei...

  20. Fluorescence, Absorption, and Excitation Spectra of Polycyclic Aromatic Hydrocarbons as a Tool for Quantitative Analysis

    ERIC Educational Resources Information Center

    Rivera-Figueroa, A. M.; Ramazan, K. A.; Finlayson-Pitts, B. J.

    2004-01-01

    A quantitative and qualitative study of the interplay between absorption, fluorescence, and excitation spectra of pollutants called polycyclic aromatic hydrocarbons (PAHs) is conducted. The study of five PAH displays the correlation of the above-mentioned properties along with the associated molecular changes.

  1. Particle in a Disk: A Spectroscopic and Computational Laboratory Exercise Studying the Polycyclic Aromatic Hydrocarbon Corannulene

    ERIC Educational Resources Information Center

    Frey, E. Ramsey; Sygula, Andrzej; Hammer, Nathan I.

    2014-01-01

    This laboratory exercise introduces undergraduate chemistry majors to the spectroscopic and theoretical study of the polycyclic aromatic hydrocarbon (PAH), corannulene. Students explore the spectroscopic properties of corannulene using UV-vis and Raman vibrational spectroscopies. They compare their experimental results to simulated vibrational…

  2. Coal-tar-based pavement sealcoat, polycyclic aromatic Hydrocarbons (PAHs), and environmental health

    USGS Publications Warehouse

    Mahler, B.J.; Van Metre, P.C.

    2011-01-01

    Studies by the U.S. Geological Survey (USGS) have identified coal-tar-based sealcoat-the black, viscous liquid sprayed or painted on asphalt pavement such as parking lots-as a major source of polycyclic aromatic hydrocarbon (PAH) contamination in urban areas for large parts of the Nation. Several PAHs are suspected human carcinogens and are toxic to aquatic life.

  3. PERSONAL EXPOSURES TO POLYCYCLIC AROMATIC HYDROCARBONS ASSOCIATED WITH THE NHEXAS PILOT

    EPA Science Inventory

    Personal exposure monitoring for select polycyclic aromatic hydrocarbons (PAHs) was performed as part of the National Human Exposure Assessment Survey (NHEXAS) Pilot Study in Baltimore, MD. Twenty-four hour PM10 sample collections (~5.7 m3) were performed using personal envi...

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

    EPA Science Inventory

    Comparative studies of the effect of polycyclic aromatic hydrocarbon geometry on the hydrolysis of diol epoxides

    The interaction of the diol epoxides (DEs) of both planar and non-planar PAHs with water have been examined using quantum mechanical and molecular dynamics. Th...

  5. Characterization of polycyclic aromatic compounds in diesel exhaust particulate extract responsible for aryl hydrocarbon receptor activity

    NASA Astrophysics Data System (ADS)

    Soontjens, Carol D.; Holmberg, Kristina; Westerholm, Roger N.; Rafter, Joseph J.

    Chemical fractions of a model diesel exhaust particulate extract, notably the fraction containing polycyclic aromatic hydrocarbons (PAH) (Fraction II), mono-nitro PAH (Fraction III), and dinitro-PAH (Fraction IV) have been shown to displace binding of 2,3,7,8-tetrachloro[1,6-[ 3H

  6. AROMATIC AND POLYCYCLIC AROMATIC HYDROCARBON FORMATION IN A LAMINAR PREMIXED N-BUTANE FLAME. (R825412)

    EPA Science Inventory

    Abstract

    Experimental and detailed chemical kinetic modeling work has been performed to investigate aromatic and polycyclic aromatic hydrocarbon (PAH) formation pathways in a premixed, rich, sooting, n-butane¯oxygen¯argon burner s...

  7. THE PHOTOTOXOICITY OF POLYCYCLIC AROMATIC HYDROCARBONS: A THEORETICAL STUDY OF EXCITED STATES AND CORRELATION TO EXPERIMENT

    EPA Science Inventory



    Investigators using models to determine the phototoxic effects of sunlight on polycyclic aromatic hydrocarbons (PAHS) have invoked the excited states of the molecule as important in elucidating the mechanism of these reactions. Energies of actual excited states were calcu...

  8. Toxicity of polycyclic aromatic hydrocarbons. (Latest citations from Pollution abstracts). Published Search

    SciTech Connect

    1995-07-01

    The bibliography contains citations concerning the toxicity and biochemical effects of aromatic polycyclic hydrocarbons. Citations discuss air, water, soil, and sediment pollution and control. Topics include vehicle emissions and control, pollutant pathways, carcinogens and mutagenic activity, and photoinduced toxicity. Food contamination, environmental monitoring, and soil contamination along highways are examined. (Contains 50-250 citations and includes a subject term index and title list.)

  9. Polycyclic aromatic hydrocarbon hazards to fish, wildlife, and invertebrates: a synoptic review

    SciTech Connect

    Eisler, R.

    1987-05-01

    The report synthesizes technical literature on ecological and toxicological aspects of polycyclic aromatic hydrocarbons (PAH) in the environment, with special reference to fisheries and wildlife resources. Subtopics include: chemical properties, sources, and fate; background concentrations in biological and nonbiological samples; toxic and sublethal effects of PAH to flora and fauna; proposed criteria and research needs for the protection of sensitive, nonhuman organisms.

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

    SciTech Connect

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

    1996-09-01

    Polycyclic aromatic hydrocarbons (PAHs) are primarily released into the environment through anthropomorphic sources. PAH degradation has been known to occur in marine sediments. This paper describes the enumeration, isolation, and preliminary characterization of PAH-degrading strains from Puget Sound sediments. 38 refs., 3 figs., 3 tabs.

  11. Bacterial biodegradation of polycyclic aromatic hydrocarbons (PAH) and potential effects of surfactants on PAH bioavailability

    SciTech Connect

    Aitken, M.D.; Grimberg, S.J.; Nagel, J.; Nagel, R.D.; Stringfellow, W.T.

    1996-02-01

    The purposes of this project were to evaluate whether indigenous microorganisms from polycyclic aromatic hydrocarbons (PAH)-contaminated soils produce surfactants (biosurfactants) as a means of enhancing the bioavailability of PAH; to improve the understanding of the general physiology of a diverse group of PAH-degrading bacteria; and to study in general how surfactants influence the biodegradation of hydrophobic chemicals.

  12. POLYCYCLIC AROMATIC HYDROCARBON BIODEGRADATION AS A FUNCTION OF OXYGEN TENSION IN CONTAMINATED SOIL

    EPA Science Inventory

    Laboratory tests were conducted to determine the effect of soil gas oxygen concentration on the degradation and mineralization of spiked 14C-pyrene and nonspiked 16 priority pollutant polycyclic aromatic hydrocarbons (PAH) present in the soil. The soil used for the evaluation was...

  13. Using urinary biomarkers to evaluate polycyclic hydrocarbon exposures in 126 preschool children in Ohio

    EPA Science Inventory

    Limited data exist on exposures of young children to polycyclic aromatic hydrocarbons (PAHs) in the United States (US). The urinary metabolite of pyrene, 1-hydroxypyrene (1-OHPyr), is widely used as a biomarker of total PAH exposure. Our objectives were to quantify urinary 1-OHPy...

  14. ANALYSIS OF POLYCYCLIC AROMATIC HYDROCARBONS BY ION TRAP TANDEM MASS SPECTROMETRY

    EPA Science Inventory

    An ion-trap mass spectrometer with a wave board and tandem mass spectrometry software was used to analyze gas chromatographically separated polycyclic aromatic hydrocarbons (PAHs) by using collision-induced dissociation (CID). The nonresonant (multiple collision) mode was used to...

  15. Determination of polycyclic aromatic hydrocarbons in biochar and biochar amended soil

    Technology Transfer Automated Retrieval System (TEKTRAN)

    A method for the determination of the 16 USEPA polycyclic aromatic hydrocarbons (PAHs) in biochar and soil amended with biochar was developed. Samples were Soxhlet extracted with acetone:cyclohexane 1:1, and PAHs were analysed by GC-MS after silica gel clean-up. In a comparative study based on reflu...

  16. EFFECT OF IRRADIANCE SPECTRA ON THE PHOTOINDUCED TOXICITY OF THREE POLYCYCLIC AROMATIC HYDROCARBONS

    EPA Science Inventory

    Photoinduced toxicity of polycyclic aromatic hydrocarbons (PAHs) is dependent on the concentration of compounds present and the dose of light received. Of the light present, only those wavelengths absorbed by the compound have the potential to initiate the photochemical events un...

  17. THE EFFECT OF IRRADIANCE SPECTRA ON THE PHOTOACTIVATED TOXICITY OF THREE POLYCYCLIC AROMATIC HYDROCARBONS

    EPA Science Inventory

    Photoinduced toxicity of polycyclic aromatic hydrocarbons (PAHs) is dependent on the concentration of compounds present and the dose of light recieved. Of the light present, only those wavelengths absorbed by the compound have the potential to initiate the photochemical events un...

  18. Environmental Behaviors and Toxicities of Polycyclic Aromatic Hydrocarbons and Nitropolycyclic Aromatic Hydrocarbons.

    PubMed

    Hayakawa, Kazuichi

    2016-01-01

    Airborne particulate matter (PM) has been collected at four cities in Japan starting in the late 1990s, at five or more major cities in China, Korea and Russia starting in 2001 and at the Noto Peninsula starting in 2004. Nine polycyclic aromatic hydrocarbons (PAHs) and eleven nitropolycyclic aromatic hydrocarbons (NPAHs) were determined by HPLC with fluorescence and chemiluminescence detections, respectively. Annual concentrations of PAHs and NPAHs were in the order, China>Russia≫Korea=Japan, with seasonal change (winter>summer). During the observation period, concentrations of PAHs and NPAHs in Japanese cities significantly decreased but the increases in the PAH concentration were observed in Chinese and Russian cities. Concentrations of PAHs and NPAHs were higher in the Northern China than those in the Southern China. At the Noto peninsula, which is in the main path of winter northwest winds and a year-round jet stream that blow from the Asian continent to Japan, the concentrations were high in winter and low in summer every year. A cluster analysis and back trajectory analysis indicated that PAHs and NPAHs were long-range transported from Northeastern China, where coal burning systems such as coal-heating boilers are considered to be the major contributors of PAHs and NPAHs. A dramatic change in atmospheric concentrations of PAHs and NPAHs in East Asia suggests the rapid and large change of PM2.5 pollution in East Asia. Considering the adverse health effects of PM2.5, continuous monitoring of atmospheric PAHs and NPAHs is necessary in this area.

  19. Polycyclic Aromatic Hydrocarbons in an industrialized urban area

    NASA Astrophysics Data System (ADS)

    Cachada, A.; Pereira, R.; Ferreira da Silva, E.; Duarte, A. C.

    2009-04-01

    Urbanization, agricultural intensification and industrialization are contributing to erosion, local and diffuse contamination and sealing of soil surfaces, resulting in soil quality degradation. Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous in urban environments and considered good markers of anthropogenic activities such as traffic, industry, domestic heating and agriculture. Although they are subject to biodegradation and photodegradation, once in the soil, they tend to bind to the soil organic fraction. Estarreja is a small coastal town in the Northwestern Portuguese coast, with a close relation with the lagoon of Aveiro which supports a variety of biotopes (channels, islands with vegetation, mudflats, salt marshes and agricultural fields) of important ecological value. It supports an intensive and diversified agriculture, a variety of heavy and light industries and a population of about half a million people which is dependent on this resource. This is a very industrialized area, due to its five decades of chemical industry. This study aims to assess the impact of the urbanization and of the chemical industry in PAHs distribution. The survey and sampling method were based on pre-interpreted maps, aerial photographs, and directly checked in the field, in order to get an overall characterization of the area. Topsoils were collected from 34 sites, considering different land uses. Five land uses were chosen: ornamental gardens, parks, roadsides, forest and agricultural. Parameters such as soil pH (ISO method 10390:1994), total C, N, H, S percentages (microanalyser LECO, CNHS-932), organic matter (LOI at 430°), particle size distribution (Micromeritics® Sedigraph 5100), cation exchange capacity and exchangeable bases, were determined in order to have a general characterization of soil. Determination of the 16 EPA PAHs in soils was performed by GC/MS after a Soxhlet extraction and an alumina clean-up of extracts. Procedure blanks, duplicates and reference

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

    PubMed

    Wang, Xianli; Kang, Haiyan; Wu, Junfeng

    2016-05-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2014-12-01

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

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

    PubMed

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

    2014-12-01

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

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

    PubMed

    Jung, Bahngmi; Batchelor, Bill

    2008-03-21

    Degradative solidification/stabilization with ferrous iron (DS/S-Fe(II)) has been found to be effective in degrading a number of chlorinated aliphatic hydrocarbons including 1,1,1-trichloroethane (1,1,1-TCA), 1,1,2,2-tetrachloroethane (1,1,2,2-TeCA), tetrachloroethylene (PCE), trichloroethylene (TCE), 1,1-dichloroethylene (1,1-DCE), vinyl chloride (VC), carbon tetrachloride (CT) and chloroform (CF). Previous studies have characterized degradation kinetics in DS/S-Fe(II) systems as affected by Fe(II) dose, pH and initial target organic concentration. The goal of this study is to investigate the importance of various chemical properties on degradation kinetics of DS/S-Fe(II). This was accomplished by first measuring rate constants for degradation of 1,1,1-TCA, 1,1,2,2-TeCA and 1,2-dichloroethane (1,2-DCA) in individual batch experiments. Rate constants developed in these experiments and those obtained from the literature were related to thermodynamic parameters including one-electron reduction potential, two-electron reduction potential, bond dissociation energy and lowest unoccupied molecular orbital energies. Degradation kinetics by Fe(II) in cement slurries were generally represented by a pseudo-first-order rate law. The results showed that the rate constants for chlorinated methanes (e.g. CT, CF) and chlorinated ethanes (e.g. 1,1,1-TCA) were higher than those for chlorinated ethylenes (e.g. PCE, TCE, 1,1-DCE and VC) under similar experimental conditions. The log of the pseudo-first-order rate constant (k) was found to correlate better with lowest unoccupied molecular orbital energies (E(LUMO)) (R2=0.874) than with other thermodynamic parameter descriptors.

  4. High molecular weight polycyclic aromatic hydrocarbons in hydrothermal petroleums - indicators of high temperatures and water washing

    SciTech Connect

    Simoneit, B.R.T.; Fetzer, J.C.

    1995-06-01

    Hydrothermal petroleums from active sedimented oceanic spreading axes contain polycyclic aromatic hydrocarbons (PAH) as characteristic components of their rapid high temperature genesis. The unsubstituted PAH dominate over their alkyl-substituted homologs and occur at high concentrations relative to the aliphatic components, which distinguishes hydrothermal petroleums from conventional reservoir petroleums. Some of the samples contain PAH with higher molecular weights than coronene (M.W. 300) and here we describe the structures and distributions of these PAH in typical examples of petroleums from Guaymas Basin, Escanaba Trough and Middle Valley. Some of the aromatic fractions (F2) show PAH of up to nine rings [e.g., dibenzo-(e,ghi)perylene, benzo(a)coronene, benzo(pqr)naphtho(8,1,2-bcd)perylene, naphtho(8,1,2-abc)coronene]. Fraction 3 in some of these samples has ovalene, a condensed ten-ring PAH. These PAH are the most thermodynamically stable structures for each ring number, and are most likely indicative of a one-ring build-up mechanism. The samples also contain a few specific PAHs [e.g., the seven-ring PAH dibenzo(cd,lm)perylene] which are not members of this stable class. Its formation mechanism must be very specific through the condensation of a pair of the three-ring phenalene radicals or through the Scholl-condensation of pyrene to a nine-ring PAH with its subsequent hydrogenation and cracking down to dibenzo(cd,lm)-perylene. This is the first report of the occurrence of heavy PAH (M.W. >300) in geological samples. They are concentrated in the bitumens by removal of the lower molecular weight PAH due to mixing during hydrothermal fluid/oil transport and selective deposition/solidification of the heavy ends at the seabed with concurrent loss of the more water soluble and lower weight products to the ambient seawater. Additional post-depositional reworking by hot fluids and biodegradation further enhance the enrichment of the heavy PAH.

  5. Nitrated polycyclic aromatic hydrocarbons in urban air particles

    SciTech Connect

    Ramdahl, T.; Becher, G.; Bjorseth, A.

    1982-12-01

    The organic extract of urban air particles from St. Louis, MO, was fractionated by high-performance liquid chromatography. The moderately polar fraction was characterized by gas chromatography-electron impact and methane negative ion chemical ionization mass spectrometry. The compounds identified in the sample included nitronaphthalene, 9-nitroanthracene, 3-nitrofluoranthene, 1-nitropyrene, arenecarbonitriles, and several polycyclic ketones, quinones, and anhydrides. These studies represent the first mass spectrometric evidence of nitroaromatics in urban air particles.

  6. H2 Ejection from Polycyclic Aromatic Hydrocarbons: Infrared Multiphoton Dissociation Study of Protonated Acenaphthene and 9,10-dihydrophenanthrene

    NASA Astrophysics Data System (ADS)

    Szczepanski, Jan; Oomens, Jos; Steill, Jeffrey D.; Vala, Martin T.

    2011-01-01

    The infrared multiple-photon dissociation (IRMPD) spectra of protonated acenaphthene ([ACN+H]+) and 9,10-dihydrophenanthrene ([DHP+H]+) have been recorded using an infrared free electron laser after the compounds were protonated by electrospray ionization and trapped in a Fourier transform ion cyclotron mass spectrometer. In both compounds, the loss of two mass units is predominant. Density functional calculations (B3LYP/6-311++G(d,p)) of the infrared spectra of all possible protonated isomers of each species showed that the observed IRMPD spectra are best fit to the isomer with the largest proton affinity and lowest relative electronic energy. Potential energy surfaces of the most stable isomers of [ACN+H]+ and [DHP+H]+ have been calculated for H and H2 loss. The lowest energy barriers are for loss of H2, with predicted energies 4.28 and 4.15 eV, respectively. After H2 ejection, the adjacent aliphatic hydrogens migrate to the bare ejection site and stabilize the remaining fragment. Single H loss may occur from [ACN+H]+ but the energy required is higher. No single H loss is predicted from [DHP+H]+, only H migration around the carbon skeleton. The vibrational bands in the parent closed-shell protonated polycyclic aromatic hydrocarbons are compared to bands observed from the interstellar medium.

  7. IMPORTANCE OF MATERNAL TRANSFER OF THE PHOTOREACTIVE POLYCYCLIC AROMATIC HYDROCARBON FLUORANTHENE FROM BENTHIC ADULT BIVALVES TO THEIR PELAGIC LARVAE

    EPA Science Inventory

    Laboratory experiments were conducted to determine if maternal transfer of polycyclic aromatic hydrocarbons (PAHs) from benthic adult bivalves could result in phototoxicity to their pelagic larvae when exposed to ultraviolet light (UV). In these experiments, adult bivalves were e...

  8. MODELING THE BINDING OF THE METABOLITES OF SOME POLYCYCLIC AROMTIC HYDROCARBONS TO THE LIGAND BINDING DOMAIN OF THE ESTROGEN RECEPTOR

    EPA Science Inventory

    Modeling the binding of the metabolites of some Polycyclic Aromatic Hydrocarbons to the ligand binding domain of the estrogen receptor
    James Rabinowitz, Stephen Little, Katrina Brown, National Health and Environmental Effects Research Laboratory, Research Triangle Park, NC; Un...

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

    EPA Science Inventory

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

  10. PHOTOACTIVATED POLYCYCLIC AROMATIC HYDROCARBON TOXICITY IN MEDAKA (ORYZIAS LATIPES) EMBRYOS: RELEVANCE TO ENVIRONMENTAL RISK IN CONTAMINATED SITES

    EPA Science Inventory

    The hazard for photoactivated toxicity of polycyclic aromatic hydrocarbons (PAHs) has been clearly demonstrated; however, to our knowledge, the risk in contaminated systems has not been characterized. To address this question, a median lethal dose (LD50) for fluoranthene photoa...

  11. IMPORTANCE OF BLACK CARBON IN DISTRIBUTION AND BIOACCUMULATION MODELS OF POLYCYCLIC AROMATIC HYDROCARBONS IN CONTAMINATED MARINE SEDIMENTS

    EPA Science Inventory

    The roles and relative importance of nonpyrogenic organic carbon (NPOC) and black carbon (BC) as binding phases of polycyclic aromatic hydrocarbons (PAHs) were assessed by their ability to estimate pore water concentrations and biological uptake in various marine sediments. Sedim...

  12. COMPARISON OF IMMUNOASSAY AND GAS CHROMATOGRAPHY/MASS SPECTROMETRY FOR MEASUREMENT OF POLYCYCLIC AROMATIC HYDROCARBONS IN CONTAMINATED SOIL

    EPA Science Inventory

    Polycyclic aromatic hydrocarbons (PAHs) are frequently encountered in the environment and may pose health concerns due to their carcinogenicity. A commercial enzyme-linked immunosorbent assay (ELISA), was evaluated as a screening method for monitoring PAHs at contaminated site...

  13. CROSS-INDUCTION OF PYRENE AND PHENANTHRENE IN MYCOBACTERIUM SP. ISOLATED FROM POLYCYCLIC AROMATIC HYDROCARBON CONTAMINATED RIVER SEDIMENTS

    EPA Science Inventory

    A polycyclic aromatic hydrocarbon (PAH)-degrading culture enriched from contaminated river sediments and a Mycobacterium sp. isolated from the enrichment were tested to investigate the possible synergistic and antagonistic interactions affecting the degradation of pyrene in the p...

  14. Renal cancer risk and occupational exposure to polycyclic aromatic hydrocarbons and plastics

    PubMed Central

    Karami, Sara; Boffetta, Paolo; Brennan, Paul; Stewart, Patricia A.; Zaridze, David; Matveev, Vsevolod; Janout, Vladimir; Kollarova, Helena; Bencko, Vladimir; Navratilova, Marie; Szeszenia-Dabrowska, Neonila; Mates, Dana; Gromiec, Jan P.; Sobotka, Roman; Chow, Wong-Ho; Rothman, Nathaniel; Moore, Lee E.

    2011-01-01

    Objective To investigate whether occupational exposure to polycyclic aromatic hydrocarbons and certain plastic monomers increased renal cell carcinomas (RCC) risk. Methods Unconditional logistic regression was used to calculate RCC risk in relation to exposure. Results No association between RCC risk and having ever been occupationally exposed to any polycyclic aromatic hydrocarbons or plastics was observed. Duration of exposure and average exposure also showed no association with risk. Suggestive positive associations between RCC risk and cumulative exposure to styrene (P-trend = 0.02) and acrylonitrile (P-trend = 0.06) were found. Cumulative exposure to petroleum/gasoline engine emissions was inversely associated with risk (P-trend = 0.02). Conclusions Results indicate a possible association between occupational styrene and acrylonitrile exposure and RCC risk. Additional studies are needed to replicate findings, as this is the first time these associations have been reported and they may be due to chance. PMID:21270648

  15. Characterization of subsurface polycyclic aromatic hydrocarbons at the Deepwater Horizon site

    NASA Astrophysics Data System (ADS)

    Diercks, Arne-R.; Highsmith, Raymond C.; Asper, Vernon L.; Joung, DongJoo; Zhou, Zhengzhen; Guo, Laodong; Shiller, Alan M.; Joye, Samantha B.; Teske, Andreas P.; Guinasso, Norman; Wade, Terry L.; Lohrenz, Steven E.

    2010-10-01

    Here, we report the initial observations of distributions of polycyclic aromatic hydrocarbons (PAH) in subsurface waters near the Deepwater Horizon oil well site (also referred to as the Macondo, Mississippi Canyon Block 252 or MC252 well). Profiles of in situ fluorescence and beam attenuation conducted during 9-16 May 2010 were characterized by distinct peaks at depths greater than 1000 m, with highest intensities close to the wellhead and decreasing intensities with increasing distance from the wellhead. Gas chromatography/mass spectrometry (GC/MS) analyses of water samples coinciding with the deep fluorescence and beam attenuation anomalies confirmed the presence of polycyclic aromatic hydrocarbons (PAH) at concentrations reaching 189 μg L-1 (ppb). Subsurface exposure to PAH at levels considered to be toxic to marine organisms would have occurred in discrete depth layers between 1000 and 1400 m in the region southwest of the wellhead site and extending at least as far as 13 km.

  16. UV irradiation of polycyclic aromatic hydrocarbons in ices: production of alcohols, quinones, and ethers

    NASA Technical Reports Server (NTRS)

    Bernstein, M. P.; Sandford, S. A.; Allamandola, L. J.; Gillette, J. S.; Clemett, S. J.; Zare, R. N.

    1999-01-01

    Polycyclic aromatic hydrocarbons (PAHs) in water ice were exposed to ultraviolet (UV) radiation under astrophysical conditions, and the products were analyzed by infrared spectroscopy and mass spectrometry. Peripheral carbon atoms were oxidized, producing aromatic alcohols, ketones, and ethers, and reduced, producing partially hydrogenated aromatic hydrocarbons, molecules that account for the interstellar 3.4-micrometer emission feature. These classes of compounds are all present in carbonaceous meteorites. Hydrogen and deuterium atoms exchange readily between the PAHs and the ice, which may explain the deuterium enrichments found in certain meteoritic molecules. This work has important implications for extraterrestrial organics in biogenesis.

  17. Fingerprint of polycyclic aromatic hydrocarbons in two populations of southern sea lions (Otaria flavescens).

    PubMed

    Marsili, L; Fossi, M C; Casini, S; Savelli, C; Jimenez, B; Junin, M; Castello, H

    1997-02-01

    The fingerprint of 14 polycyclic aromatic hydrocarbons (PAHs) was investigated in biopsy, fur, blood, liver and faeces of live and dead specimens of two Argentinian population of southern sea lion (Otaria flavescens). One colony lives in Mar del Plata harbour which is particularly polluted with petroleum, the second (control) colony lives at Punta Bermeja (Patagonia). The highest concentrations of the five carcinogenic PAHs were found in the Mar del Plata sea lions.

  18. Toxicity of aromatic polycyclic hydrocarbons. (Latest citations from the Life Sciences Collection database). Published Search

    SciTech Connect

    1997-04-01

    The bibliography contains citations concerning the toxicity and biochemical effects of aromatic polycyclic hydrocarbons. Topics include effects on metabolism and liver activity, cellular responses, binding characteristics, and the occurrence and path of the compounds in food chains. Bioaccumulation studies in specific areas, and isolation and detection techniques are also considered. (Contains 50-250 citations and includes a subject term index and title list.) (Copyright NERAC, Inc. 1995)

  19. Toxicity of polycyclic aromatic hydrocarbons. (Latest citations from Pollution abstracts). Published Search

    SciTech Connect

    Not Available

    1994-06-01

    The bibliography contains citations concerning the toxicity and biochemical effects of aromatic polycyclic hydrocarbons. Topics include effects on metabolism and liver activity, cellular responses, binding characteristics, and the occurrence and path of the compounds in food chains. Bioaccumulation studies in specific areas, and isolation and detection techniques are also considered. (Contains a minimum of 242 citations and includes a subject term index and title list.)

  20. Toxicity of aromatic polycyclic hydrocarbons. (Latest citations from the Life Sciences Collection database). Published Search

    SciTech Connect

    1995-12-01

    The bibliography contains citations concerning the toxicity and biochemical effects of aromatic polycyclic hydrocarbons. Topics include effects on metabolism and liver activity, cellular responses, binding characteristics, and the occurrence and path of the compounds in food chains. Bioaccumulation studies in specific areas, and isolation and detection techniques are also considered. (Contains 50-250 citations and includes a subject term index and title list.) (Copyright NERAC, Inc. 1995)

  1. Shape-persistent elliptic macrocycles composed of polycyclic aromatic hydrocarbons: synthesis and photophysical properties.

    PubMed

    Liu, Wen-Jun; Zhou, Yan; Zhou, Qi-Feng; Ma, Yuguo; Pei, Jian

    2008-06-05

    Bimolecular coupling/unimolecular cyclization strategies, including McMurry- and Glaser-type homocoupling reactions, were utilized to synthesize two shape-persistent elliptic macrocycles, which consist of polycyclic aromatic hydrocarbon units. The identity and purity of both macrocycles MC1 and MC2 were verified by 1H and 13C NMR, elemental analysis, as well as MALDI-TOF MS. The photophysical properties of MC1 and MC2 in dilute solution were also investigated.

  2. Synergism in the desorption of polycyclic aromatic hydrocarbons from soil models by mixed surfactant solutions.

    PubMed

    Sales, Pablo S; Fernández, Mariana A

    2016-05-01

    This study investigates the effect of a mixed surfactant system on the desorption of polycyclic aromatic hydrocarbons (PAHs) from soil model systems. The interaction of a non-ionic surfactant, Tween 80, and an anionic one, sodium laurate, forming mixed micelles, produces several beneficial effects, including reduction of adsorption onto solid of the non-ionic surfactant, decrease in the precipitation of the fatty acid salt, and synergism to solubilize PAHs from solids compared with individual surfactants.

  3. Toxicity to Daphnia pulex and QSAR predictions for polycyclic hydrocarbons representative of Great Lakes contaminants

    USGS Publications Warehouse

    Passino-Reader, D.R.; Hickey, J.P.; Ogilvie, L.M.

    1997-01-01

    The objectives of this study were (1) to determine the toxicity of several types of polycyclic hydrocarbons characteristic of Great Lakes samples to Daphnia pulex, a Great Lakes zooplankter, (2) to investigate the influence of different structural characteristics on toxicity, and (3) to determine the linear solvation energy relationship (LSER) parameters and model that describe these compounds. These results will be related to comparative toxicity of other Great Lakes environmental compounds and to their application in site specific risk assessment.

  4. Air sampling and determination of vapours and aerosols of bitumen and polycyclic aromatic hydrocarbons in the Human Bitumen Study.

    PubMed

    Breuer, Dietmar; Hahn, Jens-Uwe; Höber, Dieter; Emmel, Christoph; Musanke, Uwe; Rühl, Reinhold; Spickenheuer, Anne; Raulf-Heimsoth, Monika; Bramer, Rainer; Seidel, Albrecht; Schilling, Bernd; Heinze, Evelyn; Kendzia, Benjamin; Marczynski, Boleslaw; Welge, Peter; Angerer, Jürgen; Brüning, Thomas; Pesch, Beate

    2011-06-01

    The chemical complexity of emissions from bitumen applications is a challenge in the assessment of exposure. Personal sampling of vapours and aerosols of bitumen was organized in 320 bitumen-exposed workers and 69 non-exposed construction workers during 2001-2008. Area sampling was conducted at 44 construction sites. Area and personal sampling of vapours and aerosols of bitumen showed similar concentrations between 5 and 10 mg/m(3), while area sampling yielded higher concentrations above the former occupational exposure limit (OEL) of 10 mg/m(3). The median concentration of personal bitumen exposure was 3.46 mg/m(3) (inter-quartile range 1.80-5.90 mg/m(3)). Only few workers were exposed above the former OEL. The specificity of the method measuring C-H stretch vibration is limited. This accounts for a median background level of 0.20 mg/m³ in non-exposed workers which is likely due to ubiquitous aliphatic hydrocarbons. Further, area measurements of polycyclic aromatic hydrocarbons (PAHs) were taken at 25 construction sites. U.S. EPA PAHs were determined with GC/MS, with the result of a median concentration of 2.47 μg/m(3) at 15 mastic asphalt worksites associated with vapours and aerosols of bitumen, with a Spearman correlation coefficient of 0.45 (95% CI -0.13 to 0.78). PAH exposure at mastic-asphalt works was higher than at reference worksites (median 0.21 μg/m(3)), but about one order of magnitude lower compared to coke-oven works. For a comparison of concentrations of vapours and aerosols of bitumen and PAHs in asphalt works, differences in sampling and analytical methods must to be taken into account.

  5. Emission characteristics of polycyclic aromatic hydrocarbons and nitro-polycyclic aromatic hydrocarbons from diesel trucks based on on-road measurements

    NASA Astrophysics Data System (ADS)

    Cao, Xinyue; Hao, Xuewei; Shen, Xianbao; Jiang, Xi; Wu, Bobo; Yao, Zhiliang

    2017-01-01

    Polycyclic aromatic hydrocarbon (PAH) and nitro-polycyclic aromatic hydrocarbon (NPAH) emissions from 18 diesel trucks of different sizes and with different emission standards were tested in Beijing using a portable emission measurement system (PEMS). Both the gaseous- and particulate-phase PAHs and NPAHs were quantified by high-performance liquid chromatography (HPLC) in the laboratory. The emission factors (EFs) of the total PAHs from light-duty diesel trucks (LDDTs), medium-duty diesel trucks (MDDTs) and heavy-duty diesel trucks (HDDTs) were 82229.11 ± 41906.06, 52867.43 ± 18946.47 and 93837.35 ± 32193.14 μg/km, respectively, much higher than the respective values of total NPAHs from their counterpart vehicles. The gaseous phase had an important contribution to the total PAHs and NPAHs, with a share rate of approximately 69% and 97% on average, respectively. The driving cycle had important impacts on the emissions of PAHs and NPAHs, especially for LDDTs and HDDTs. Higher emissions of PAHs and NPAHs were detected on non-highway roads compared to that on highways for these two types of vehicles. Compared to the results of different studies, the difference in the EFs of PAHs and NPAHs can reach several orders of magnitudes, which would introduce errors in the development of an emission inventory of PAHs and NPAHs.

  6. Forensic investigation of aliphatic hydrocarbons in the sediments from selected mangrove ecosystems in the west coast of Peninsular Malaysia.

    PubMed

    Vaezzadeh, Vahab; Zakaria, Mohamad Pauzi; Shau-Hwai, Aileen Tan; Ibrahim, Zelina Zaiton; Mustafa, Shuhaimi; Abootalebi-Jahromi, Fatemeh; Masood, Najat; Magam, Sami Mohsen; Alkhadher, Sadeq Abdullah Abdo

    2015-11-15

    Peninsular Malaysia has gone through fast development during recent decades resulting in the release of large amounts of petroleum and its products into the environment. Aliphatic hydrocarbons are one of the major components of petroleum. Surface sediment samples were collected from five rivers along the west coast of Peninsular Malaysia and analyzed for aliphatic hydrocarbons. The total concentrations of C10 to C36 n-alkanes ranged from 27,945 to 254,463ng·g(-1)dry weight (dw). Evaluation of various n-alkane indices such as carbon preference index (CPI; 0.35 to 3.10) and average chain length (ACL; 26.74 to 29.23) of C25 to C33 n-alkanes indicated a predominance of petrogenic source n-alkanes in the lower parts of the Rivers, while biogenic origin n-alkanes from vascular plants are more predominant in the upper parts, especially in less polluted areas. Petrogenic sources of n-alkanes are predominantly heavy and degraded oil versus fresh oil inputs.

  7. [Halogenated polycyclic aromatic hydrocarbons in surface sediments of Maozhou River, Shenzhen].

    PubMed

    Sun, Jian-Lin; Ni, Hong-Gang; Ding, Chao; Zeng, Hui

    2012-09-01

    Surface sediments collected from the Maozhou River watershed in Shenzhen were analyzed for the concentration levels and spatial distribution characteristics of halogenated polycyclic aromatic hydrocarbons (HPAHs) using GC-MS. Total concentrations of three chlorinated polycyclic aromatic hydrocarbons (ClPAHs) and six brominated polycyclic aromatic hydrocarbons (BrPAHs) of concern ranged from 3.00 to 301 ng x g(-1) and 7.52 to 285 ng x g(-1), respectively. Source appointments indicated that the HPAHs in these surface sediments were mainly derived from waste incineration, fossil fuel combustion, vehicle emission, and burning of crop straw, accounting for 40%, 20.5% 11.9%, and 11.7% of the total loading, respectively. Additionally, the toxic equivalency quotients (TEQ) of total ClPAHs and BrPAHs ranged from 7.95 to 38.1 pg x g(-1) and 38.1 to 105 pg x g(-1) respectively. Finally, the relationships between the HPAHs levels and different land use types were examined. Results indicated that the levels of HPAHs in surface sediments showed a decreasing trend after the first increase to the peak with the density of industrial land, but inversely proportional to the density of agricultural land.

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

    PubMed

    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.

  9. Microbial metabolism of polycyclic aromatic hydrocarbons: isolation and characterization of a pyrene-degrading bacterium.

    PubMed Central

    Heitkamp, M A; Franklin, W; Cerniglia, C E

    1988-01-01

    Microbiological analyses of sediments located near a point source for petrogenic chemicals resulted in the isolation of a pyrene-mineralizing bacterium. This isolate was identified as a Mycobacterium sp. on the basis of its cellular and colony morphology, gram-positive and strong acid-fast reactions, diagnostic biochemical tests, 66.6% G + C content of the DNA, and high-molecular-weight mycolic acids (C58 to C64). The mycobacterium mineralized pyrene when grown in a mineral salts medium supplemented with nutrients but was unable to utilize pyrene as a sole source of carbon and energy. The mycobacterium grew well at 24 and 30 degrees C and minimally at 35 degrees C. No growth was observed at 5 or 42 degrees C. The mycobacterium grew well at salt concentrations up to 4%. Pyrene-induced Mycobacterium cultures mineralized 5% of the pyrene after 6 h and reached a maximum of 48% mineralization within 72 h. Treatment of induced and noninduced cultures with chloramphenicol showed that pyrene-degrading enzymes were inducible in this Mycobacterium sp. This bacterium could also mineralize other polycyclic aromatic hydrocarbons and alkyl- and nitro-substituted polycyclic aromatic hydrocarbons including naphthalene, phenanthrene, fluoranthene, 3-methylcholanthrene, 1-nitropyrene, and 6-nitrochrysene. This is the first report of a bacterium able to extensively mineralize pyrene and other polycyclic aromatic hydrocarbons containing four aromatic rings. Images PMID:3202633

  10. Structure-biodegradability relationships of polycyclic aromatic hydrocarbons in soil

    SciTech Connect

    Bossert, I.D.; Bartha, R.

    1986-10-01

    In a previous study on oily sludge disposal by land treatment, PAH as a class were found to be biodegraded more rapidly than the total solvent-extractable hydrocarbons of the sludge. This somewhat surprising result was apparently due to a predominance of low molecular weight PAH (less than or equal to 3 rings) in the sludge sample. The higher molecular weight PAH (greater than or equal to 4 rings) exhibited persistence that seemed to increase with the number of rings and the degree of ring condensation. In order to verify and extend these observations, the authors have undertaken here a systematic study on the structure-biodegradability relationship (SBR) of PAH in soil. Since it was expected that the majority of the PAH would be degraded cometabolically rather than in the substrate utilization mode, 1-phenyldecane was added as primary substrate in combination with all the PAH tested. In preliminary tests, 1-phenyldecane proved to be more effective in stimulating the biodegradation of 1,2-benzpyrene (benzo(a)pyrene) than either n-hexadecane, naphthoic acid or sewage sludge. The presence of an additional hydrocarbon substrate made this SBR study also more relevant to our previous work on the fate of PAH during the disposal of oily sludges by land treatment.

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

    PubMed

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

    2015-12-25

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

  12. Isolation and gas-chromatographic determination of saturated and polycyclic aromatic hydrocarbons in mussels

    SciTech Connect

    Butler, A.C.; Sibbald, R.R.

    1986-10-01

    The method here presented is intended for application in the analysis of trace quantities of petroleum hydrocarbons in oil-polluted mussels. It is a technique incorporating saponification, pentane extraction and silica gel cleanup, and represents a modification and ad hoc synthesis of other procedures. Recovery efficiencies of the method are 80% or greater for C/sub 15/ to C/sub 38/ n-alkanes, and vary between 0% for naphthalene and 84% for pyrene. Isolation and quantification of the polycyclic aromatic hydrocarbon (PAH) fraction are of importance in environmental monitoring; some compounds in this group are either known or suspected to be carcinogenic agents. Concomitant analysis for the saturated hydrocarbons fraction can provide essential clues to the petrogenic or pyrolytic origin of the PAHs.

  13. Isolation and gas-chromatographic determinations of saturated and polycyclic aromatic hydrocarbons in mussels

    SciTech Connect

    Bulter, A.C.; Sibbald, R.R.

    1986-10-01

    The method here presented is intended for application in the analysis of trace quantities of petroleum hydrocarbons in oil-polluted mussels. It is a technique incorporating saponification, pentane extraction and silica gel cleanup, and represents a modification and ad hoc synthesis of other procedures. Recovery efficiencies of the method are 80% or greater for C/sub 15/ to C/sub 38/ n-alkanes, and vary between 0% for naphthalene and 84% for pyrene. Isolation and quantification of the polycyclic aromatic hydrocarbon (PAH) fraction are of importance in environmental monitoring; some compounds in this group are either known or suspected to be carcinogenic agents. Concomitant analysis for the saturated hydrocarbons fraction can provide essential clues to the petrogenic or pyrolytic origin of the PAHs.

  14. 40 CFR Table 2b to Subpart E of... - Reactivity Factors for Aliphatic Hydrocarbon Solvent Mixtures

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... Alkanes (2 to 460-580 Alkanes (8 to 22% Aromatics) 1.49 * Average Boiling Point = (Initial Boiling Point + Dry Point) / 2 (b) Aromatic Hydrocarbon Solvents ... Hydrocarbon Solvent Mixtures Bin Averageboiling point * (degrees F) Criteria Reactivityfactor 1 80-205...

  15. 40 CFR Table 2b to Subpart E of... - Reactivity Factors for Aliphatic Hydrocarbon Solvent Mixtures

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...-580 Alkanes (2 to 460-580 Alkanes (8 to 22% Aromatics) 1.49 * Average Boiling Point = (Initial Boiling Point + Dry Point)/2(b) Aromatic Hydrocarbon Solvents ... Hydrocarbon Solvent Mixtures Bin Averageboiling point* (degrees F) Criteria Reactivityfactor (g O3/g VOC) 1...

  16. 40 CFR Table 2b to Subpart E of... - Reactivity Factors for Aliphatic Hydrocarbon Solvent Mixtures

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...-580 Alkanes (2 to 460-580 Alkanes (8 to 22% Aromatics) 1.49 * Average Boiling Point = (Initial Boiling Point + Dry Point)/2(b) Aromatic Hydrocarbon Solvents ... Hydrocarbon Solvent Mixtures Bin Averageboiling point* (degrees F) Criteria Reactivityfactor (g O3/g VOC) 1...

  17. 40 CFR Table 2b to Subpart E of... - Reactivity Factors for Aliphatic Hydrocarbon Solvent Mixtures

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...-580 Alkanes (2 to 460-580 Alkanes (8 to 22% Aromatics) 1.49 * Average Boiling Point = (Initial Boiling Point + Dry Point)/2(b) Aromatic Hydrocarbon Solvents ... Hydrocarbon Solvent Mixtures Bin Averageboiling point* (degrees F) Criteria Reactivityfactor (g O3/g VOC) 1...

  18. 40 CFR Table 2b to Subpart E of... - Reactivity Factors for Aliphatic Hydrocarbon Solvent Mixtures

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... Alkanes (2 to 460-580 Alkanes (8 to 22% Aromatics) 1.49 * Average Boiling Point = (Initial Boiling Point + Dry Point) / 2 (b) Aromatic Hydrocarbon Solvents ... Hydrocarbon Solvent Mixtures Bin Averageboiling point * (degrees F) Criteria Reactivityfactor 1 80-205...

  19. A Review on the Genetics of Aliphatic and Aromatic Hydrocarbon Degradation.

    PubMed

    Abbasian, Firouz; Lockington, Robin; Megharaj, Mallavarapu; Naidu, Ravi

    2016-01-01

    Because of the high diversity of hydrocarbons, degradation of each class of these compounds is activated by a specific enzyme. However, most of other downstream enzymes necessary for complete degradation of hydrocarbons maybe common between different hydrocarbons. The genes encoding proteins for degradation of hydrocarbons, including the proteins required for the uptake of these molecules, the specific enzyme used for the initial activation of the molecules and other necessary degrading enzymes are usually arranged as an operon. Although the corresponding genes in many phylogenetic groups of microbial species show different levels of diversity in terms of the gene sequence, the organisation of the genes in the genome or on plasmids and the activation mode (inductive or constitutive), some organisms show identical hydrocarbon-degrading genes, probably as a result of horizontal gene transfer between microorganisms.

  20. Aliphatic Hydrocarbons and Fatty Acids of Some Marine and Freshwater Microorganisms

    PubMed Central

    Oró, J.; Tornabene, T. G.; Nooner, D. W.; Gelpi, E.

    1967-01-01

    Gas chromatography and combined gas chromatography-mass spectrometry have been used to study the fatty acids and hydrocarbons of a bacterium from the Pacific Ocean, Vibrio marinus, a freshwater blue-green alga, Anacystis nidulans, and algal mat communities from the Gulf of Mexico. Both types of microorganisms (bacteria and algae) showed relatively simple hydrocarbon and fatty acid patterns, the hydrocarbons predominating in the region of C-17 and the fatty acids in the range of C-14 to C-18. The patterns of V. marinus were more comparable to those of the algal populations than to patterns reported for other bacteria. An incomplete correlation between fatty acids and hydrocarbons in both types of organisms was observed, making it difficult to accept the concept that the biosynthesis of hydrocarbons follows a simple fatty acid decarboxylation process. PMID:6025301

  1. In-Situ Heating Decrease Kinetics of Aliphatic Hydrocarbons in Tagish Lake Meteorite by Micro-FTIR

    NASA Technical Reports Server (NTRS)

    Kebukawa, Y.; Nakashima, S.; Zolensky, M. E.

    2005-01-01

    Carbonaceous chondrites are known to contain up to 3wt.% C, the major part of which corresponds to a macromolecular organic fraction. Chondritic organic matter is based on small aromatic units, cross-linked by short aliphatic chains rather than large clusters of polyaromatic structures. Two main characteristic features of those organics measured by FTIR are: (1) an equivalent intensity of the asymmetric stretching mode absorptions for CH3 (2960/cm) and CH2 (2920/cm) and (2) a lack of aromatic CH-stretching mode (3040/cm). Tagish Lake is a new type of water- and carbon-rich type 2 carbonaceous chondrite. Its total carbon content is approx. 5 wt%, of which the organic carbon content reaches approx. 1.3 wt%. Tagish Lake may have never experienced temperatures higher than 120 C after formation of organics based on the disappearance of infrared (IR) organic peaks in step heating experiments. Here we report in-situ kinetic heating experiments of organics in Tagish Lake by micro-FTIR to characterize the nature of aliphatic hydrocarbons and their thermal stabilities.

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

    NASA Astrophysics Data System (ADS)

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

    2009-04-01

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

  3. Docosahexaenoic acid regulates gene expression in HUVEC cells treated with polycyclic aromatic hydrocarbons.

    PubMed

    Gdula-Argasińska, Joanna; Czepiel, Jacek; Totoń-Żurańska, Justyna; Jurczyszyn, Artur; Perucki, William; Wołkow, Paweł

    2015-07-16

    The molecular mechanism of inflammation and carcinogenesis induced by exposure of polycyclic aromatic hydrocarbons (PAHs) is not clearly understood. Our study was undertaken due to the strong pro-carcinogenic potential and reactivity of PAH-metabolites, as well as the susceptibility of polyunsaturated fatty acids to oxidation. The aim of this study was to evaluate the pro- or anti-inflammatory impact of n-3 docosahexaenoic acid on human primary umbilical vein endothelial cells (HUVEC) exposed to polycyclic aromatic hydrocarbons. We analysed the influence of docosahexaenoic acid (DHA) and/or PAHs supplementation on the fatty acid profile of cell membranes, on cyclooxygenase-2 (COX-2), aryl hydrocarbon receptor (AHR), and glutathione S transferase Mu1 (GSTM1) protein expression as well as on the prostaglandin synthase 2 (PTGS2), AHR, GSTM1, PLA2G4A, and cytochrome P450 CYP1A1 gene expression. We observed that COX-2 and AHR protein expression was increased while GSTM1 expression was decreased in cells exposed to DHA and PAHs. Docosahexaenoic acid down-regulated CYP1A1 and up-regulated the AHR and PTGS2 genes. Our findings suggested that DHA contributes significantly to alleviate the harmful effects caused by PAHs in endothelial cells. Moreover, these results suggest that a diet rich in n-3 fatty acids is helpful to reduce the harmful effects of PAHs exposure on human living in heavily polluted areas.

  4. Fully Deuterated Aliphatic Hydrocarbons Obtained From Iron Carbide Treated with DCl and D2O

    NASA Technical Reports Server (NTRS)

    Marquez, C.; Lazcano, A.; Miller, S. L.; Oro, J.

    1966-01-01

    According to Oparin, Mendeleev thought that the origin of petroleum was the result of the hydrolysis of iron carbides by superheated steam under pressure from the deep interior of the Earth through geological formations where the metal carbides exist. As early as 1877, Mendeleev described the reaction leading to the synthesis of hydrocarbons according to the general equation 3Fe(sub m)C(sub n) + mH2O yields mFe3O4 + C(sub 3n)H(sub 8m). Other experimental studies on the production of hydrocarbons from cast iron have been reported. Because of the possibility that hydrocarbons may have been trapped within the carbon matrix of the cast iron, which usually has a high content of carbon, we have studied the reaction of pure iron carbide with deuterium chloride and deuterated water. This was done in order to distinguish any newly formed deuterated hydrocarbons from any possible impurities of trapped hydrocarbons. The experiments were carried out by simply allowing iron carbide to react with concentrated deuterium chloride in D2O. The volatile hydrocarbon fraction examined by gas chromatography-mass spectrometry (GC/MS), using a Finnigan 1020/OWA instrument. contained low molecular weight hydrocarbons in a range C3 to C7. Lower molecular weight hydrocarbons were not detected by GC/MS because the MS scanning mode was preset above mass 40 to exclude components of air. The identified hydrocarbons are similar to those obtained under prebiotic conditions using high frequency discharge. The hydrocarbons found in common were propane, butane, pentane, 3-methylpentane, hexane, and heptane. The percent yields decline with increasing carbon number (propane 11%, n-heptane 1%). Similar results have been obtained by the direct treatment of metal carbides by pulse laser vaporization mass spectrometry. These results show that the hydrolysis of iron carbides may have been a significant source of hydrocarbons on the primitive Earth. There appears to be a predominance of straight chain

  5. Magnetic ionic liquids as non-conventional extraction solvents for the determination of polycyclic aromatic hydrocarbons.

    PubMed

    Trujillo-Rodríguez, María J; Nacham, Omprakash; Clark, Kevin D; Pino, Verónica; Anderson, Jared L; Ayala, Juan H; Afonso, Ana M

    2016-08-31

    This work describes the applicability of magnetic ionic liquids (MILs) in the analytical determination of a group of heavy polycyclic aromatic hydrocarbons. Three different MILs, namely, benzyltrioctylammonium bromotrichloroferrate (III) (MIL A), methoxybenzyltrioctylammonium bromotrichloroferrate (III) (MIL B), and 1,12-di(3-benzylbenzimidazolium) dodecane bis[(trifluoromethyl)sulfonyl)]imide bromotrichloroferrate (III) (MIL C), were designed to exhibit hydrophobic properties, and their performance examined in a microextraction method for hydrophobic analytes. The magnet-assisted approach with these MILs was performed in combination with high performance liquid chromatography and fluorescence detection. The study of the extraction performance showed that MIL A was the most suitable solvent for the extraction of polycyclic aromatic hydrocarbons and under optimum conditions the fast extraction step required ∼20 μL of MIL A for 10 mL of aqueous sample, 24 mmol L(-1) NaOH, high ionic strength content of NaCl (25% (w/v)), 500 μL of acetone as dispersive solvent, and 5 min of vortex. The desorption step required the aid of an external magnetic field with a strong NdFeB magnet (the separation requires few seconds), two back-extraction steps for polycyclic aromatic hydrocarbons retained in the MIL droplet with n-hexane, evaporation and reconstitution with acetonitrile. The overall method presented limits of detection down to 5 ng L(-1), relative recoveries ranging from 91.5 to 119%, and inter-day reproducibility values (expressed as relative standard derivation) lower than 16.4% for a spiked level of 0.4 μg L(-1) (n = 9). The method was also applied for the analysis of real samples, including tap water, wastewater, and tea infusion.

  6. Speciation of atmospheric polycyclic aromatic hydrocarbons (PAHs) present during fog time collected submicron particles.

    PubMed

    Singh, Dharmendra Kumar; Sharma, Swati; Habib, Gazala; Gupta, Tarun

    2015-08-01

    Airborne submicron particles (PM1) were collected using PM1 sampler during the fog-dominated days (December 2013-January 2014). PM1 values varied between 58.12 μg/m(3) and 198.75 μg/m(3), and average mass concentration was 162.33 ± 38.25 μg/m(3) while total average concentration of particle-associated polycyclic aromatic hydrocarbon (PAHs) determined was 616.31 ± 30.31 ng/m(3). This is a signal for an alarming high pollution level at this site situated in the Indo-Gangetic Plain (IGP). PAHs were extracted from filters using toluene and acetonitrile. Quantitative measurements of polycyclic aromatic hydrocarbons (PAHs) were carried out using the high performance liquid chromatography (HPLC) technique. The extracts were analyzed for 16 target polycyclic aromatic hydrocarbons (PAHs) including carcinogenic compound benzo(a)pyrene (19.86 ± 38.98 ng/m(3)). Fluoranthene, benzo(a)anthracene, anthracene, and fluorene were the predominant compounds found in the samples collected during foggy days. Based on number of rings, four-ring PAH compounds had maximum contribution (43%) in this fog time collected submicron particles followed by three-ring (21%), five-ring (20%), six-ring (13%), and two-ring (3%), respectively. In winter and foggy days, wood and coal combustion and biomass burning also significantly contribute to the PAH levels. However, diagnostic ratio suggests diesel emissions as the prime source of PAHs at this sampling site.

  7. Biodegradation aspects of polycyclic aromatic hydrocarbons (PAHs): a review.

    PubMed

    Haritash, A K; Kaushik, C P

    2009-09-30

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

  8. Influence of peanut oil on microbial degradation of polycyclic aromatic hydrocarbons.

    PubMed

    Pannu, Jasvir K; Singh, Ajay; Ward, Owen P

    2003-08-01

    Peanut oil amendment (0.1%-0.2% (v/v)) increased the biodegradation of various polycyclic aromatic hydrocarbons (PAHs) by 15%-80% with a mixed bacterial culture and a pure culture of Comamonas testosteroni in aqueous media and in PAH-contaminated weathered soil slurry systems. The stimulatory effect on biodegradation was more pronounced with the high molecular weight PAHs (e.g., >3 rings). The presence of peanut oil also accelerated the biodegradation of PAHs sorbed onto activated carbon, indicating its potential application in the bioregeneration of activated carbon.

  9. Emission of polycyclic aromatic hydrocarbons from light-duty diesel vehicles exhaust

    NASA Astrophysics Data System (ADS)

    de Abrantes, Rui; de Assunção, João V.; Pesquero, Célia R.

    Standardised tests were performed on four light-duty diesel vehicles running in a chassis dynamometer at a vehicular emission laboratory, using the FTP-75 test cycle procedure. The aim was to characterise emissions of Polycyclic Aromatic Hydrocarbons (PAHs), substances that create health hazards and are, as yet, unregulated. The pollutants were analysed in both solid and gaseous phases using high-performance liquid chromatography. Total PAH values ranged from 1.133 to 5.801 mg km -1. Naphthalene, phenanthrene, fluoranthene, pyrene and chrysene were detected in all tests. In addition, PAH emission was observed to be inversely related to emission of CO 2.

  10. A new emission feature in IRAS spectra and the polycyclic aromatic hydrocarbon spectrum

    NASA Technical Reports Server (NTRS)

    Cohen, M.; Tielens, A. G. G. M.; Allamandola, L. J.

    1985-01-01

    IRAS spectra of those sources which show strong 7.7 and 11.3 micron emission features also show a plateau of emission extending from 11.3 to about 13.0 microns. Like the 11.3 micron feature, this new feature is attributed to the CH out-of-plane bending mode in polycyclic aromatic hydrocarbons (PAHs). Its discovery reinforces the identification of the 'unidentified infrared emission features' as emission from PAHs. The wavelength of this new feature suggests that interstellar PAHs are not as partially hydrogenated as hitherto thought. It also constrains their molecular structure.

  11. Evidence that Polycyclic Aromatic Hydrocarbons in Two Carbonaceous Chondrites Predate Parent-Body Formation

    NASA Technical Reports Server (NTRS)

    Plows, F. L.; Elsila, J. E.; Zare, R. N.; Buseck, P. R.

    2003-01-01

    Organic material in meteorites provides insight into the cosmochemistry of the early solar system. The distribution of polycyclic aromatic hydrocarbons (PAHs) in the Allende and Murchison carbonaceous chondrites was investigated using spatially resolved microprobe laser-desorption laser-ionization mass spectrometry. Sharp chemical gradients of PAHs are associated with specific meteorite features. The ratios of various PAH intensities relative to the smallest PAH, naphthalene, are nearly constant across the sample. These findings suggest a common origin for PAHs dating prior to or contemporary with the formation of the parent body, consistent with proposed interstellar formation mechanisms.

  12. Interrelationship of Pyrogenic Polycyclic Aromatic Hydrocarbon (PAH) Contamination in Different Environmental Media

    PubMed Central

    Kim, Seung-Kyu; Lee, Dong Soo; Shim, Won Joon; Yim, Un Hyuk; Shin, Yong-Seung

    2009-01-01

    Interrelationships between pyrogenic polycyclic aromatic hydrocarbons (PAHs) were assessed in air, soil, water, sediment, and tree leaves by using multi-media monitoring data. Concurrent concentration measurements were taken bimonthly for a year for the multi-media at urban and suburban sites. PAH level correlations between air and other media were observed at the urban site but were less clear at the suburban site. Considering a closer PAHs distribution/fate characteristics to soil than suspended solids, contamination in sediment seemed to be governed primarily by that in soil. The partitioning of PAHs in waters could be better accounted for by sorption onto black carbon and dissolved organic carbon. PMID:22303141

  13. Detection of Medium-Sized Polycyclic Aromatic Hydrocarbons via Fluorescence Energy Transfer

    PubMed Central

    Serio, Nicole; Prignano, Lindsey; Peters, Sean; Levine, Mindy

    2015-01-01

    Reported herein is the use of proximity-induced non-covalent energy transfer for the detection of medium-sized polycyclic aromatic hydrocarbons (PAHs). This energy transfer occurs within the cavity of γ-cyclodextrin in various aqueous environments, including human plasma and coconut water. Highly efficient energy transfer was observed, and the efficiency of the energy transfer is independent of the concentration of γ-cyclodextrin used, demonstrating the importance of hydrophobic binding in facilitating such energy transfer. Low limits of detection were also observed for many of the PAHs investigated, which is promising for the development of fluorescence-based detection schemes. PMID:25821390

  14. Interstellar polycyclic aromatic hydrocarbons and carbon in interplanetary dust particles and meteorites

    NASA Astrophysics Data System (ADS)

    Allamandola, L. J.; Sandford, S. A.; Wopenka, B.

    1987-07-01

    Raman spectra of interplanetary dust particles (IDPs) and meteorites containing material similar to polycyclic aromatic hydrocarbons (PAHs) show features that are similar in position and relative strength to interstellar IR emission features attributable to vibrational transitions in free molecular-sized PAHs. In addition, these spectra sometimes show red photoluminescence that has elsewhere been attributed to PAHs, and a part of the carbonaceous phase in IDPs and meteorites contain a degree of deuterium enrichment anticipated in small, free PAHs that are exposed to ISM UV radiation. These observations suggest that some of the IDPs' carbonaceous material may have been produced in circumstellar dust shells, and only slightly modified in interstellar space.

  15. THE FAR-INFRARED SPECTROSCOPY OF VERY LARGE NEUTRAL POLYCYCLIC AROMATIC HYDROCARBONS

    SciTech Connect

    Ricca, Alessandra; Bauschlicher, Charles W.; Mattioda, Andrew L.; Boersma, Christiaan; Allamandola, Louis J.

    2010-01-20

    Here we report the computed far-infrared (FIR) spectra of neutral polycyclic aromatic hydrocarbon (PAH) molecules containing at least 82 carbons up to 130 carbons and with shapes going from compact round and oval-type structures to rectangular and to trapezoidal. The effects of size and shape on the FIR band positions and intensities are discussed. Using FIR data from the NASA Ames PAH IR Spectroscopic Database Version 1.1, we generate synthetic spectra that support the suggestion that the 16.4, 17.4, and 17.8 mum bands arise from PAHs.

  16. Characteristics of wintertime polycyclic aromatic hydrocarbon assemblage in aerosol of the Southern Adriatic

    NASA Astrophysics Data System (ADS)

    Jovanović, V. Ž.; Pfendt, P. A.; Filipović, A. J.

    2007-09-01

    Features of polycyclic aromatic hydrocarbon (PAH) assemblage in aerosol samples collected from the atmosphere of Herceg Novi during the winter months of two successive years were studied. The results showed almost the same concentration profiles of identified PAHs for samples from the two periods analyzed, generally suggesting a similar origin. Diagnostic ratios indicated combustion of wood and coal, emissions from petrol and diesel engines, and dust resuspension as sources that predominantly contributed to the atmospheric PAH concentrations. Statistical analysis, principal component analysis (PCA) in particular, allowed us to identify the impact of meteorological parameters on PAH abundance.

  17. Assessment of polycyclic aromatic hydrocarbon input to urban wetlands in relation to adjacent land use.

    PubMed

    Kimbrough, K L; Dickhut, R M

    2006-11-01

    The relationship between polycyclic aromatic hydrocarbons (PAHs) in wetland surface sediments and adjacent land use was assessed in the Elizabeth River, VA, an urbanized sub-estuary of the Chesapeake Bay. Significant differences (p<0.05) in surface sediment PAH concentration between sites indicated adjacent land use had a substantial influence on PAH concentration in wetland sediments. Wetlands adjacent to parking lots and petroleum industrial sites exhibited the highest PAH concentrations of all wetlands examined. Overall, commercial land uses had the highest PAH concentrations and automotive sources dominated (52-69%) PAH input to wetland surface sediments irrespective of adjacent land use.

  18. Spectral studies of polycyclic aromatic hydrocarbon interaction with human blood plasma

    NASA Astrophysics Data System (ADS)

    Melnikov, A. G.; Pravdin, A. B.; Kochubey, V. I.; Melnikov, G. V.

    2006-08-01

    Analysis of fluorescence spectra of polycyclic aromatic hydrocarbons in human blood plasma and human serum albumin solution allowed one to conclude that pyrene and also anthracene are predominantly distributed in the hydrophobic micro-phase of blood plasma proteins. In the solution of human blood plasma containing pyrene the nonmonotonic dependence of both the intensity of pyrene fluorescence and the index of polarity on the concentration of sodium dodecylsulfate added was observed. This should be connected with the reconstruction of the structure of protein globule under the surfactant action and cannot be explained only by the solubilization of pyrene in sodium dodecylsulfate micelles.

  19. Qsars for photoinduced toxicity: 1. acute lethality of polycyclic aromatic hydrocarbons to daphnia magna'

    SciTech Connect

    Mekenyan, O.G.; Ankley, G.T.; Veith, G.D.; Call, D.J.

    1994-01-01

    Research with a variety of aquatic species has shown that while polycyclic aromatic hydrocarbons (PAHs) are generally not acutely toxic in conventional laboratory tests, many are extremely toxic in the presence of sunlight. In an effort to develop a model for predicting which PAHs may exhibit photo-induced toxicity, Newsted and Giesy (1987) reported a parabolic relationship between the toxicity and the energy of the triplet state of a variety of PAHs. The authors have reexamined these data and propose a more mechanistic explanation for the prediction of photo-induced PAH toxicity. They sought a molecular descriptor which could be computed from structure rather than measured empirically.

  20. Genotoxicity of nitrated polycyclic aromatic hydrocarbons and related structures on Escherichia coli PQ37 (SOS chromotest)

    SciTech Connect

    Mersch-Sundermann, V.; Kern, S.; Wintermann, F. )

    1991-01-01

    To determine the genotoxicity of nitrated polycyclic aromatic hydrocarbons and related molecules (nPAH) the authors examined 24 compounds representative of nitroanthracenes, nitrofluorenes, nitronaphthalenes, nitropyrenes, and nitroquinolines for genotoxicity in Escherichia coli PQ37 (SOS-chromotest). To enhance the sensitivity of the tester strain and optimize metabolic activation they used a modified test protocol and S9-mix composition. As expected from previously referred mutagenicity studies, the highest SOS inducing potencies (SOSIP) were exhibited by the dinitropyrenes, 4-nitroquinoline-N-oxide, and 3-nitrofluoranthese. The results were compared to those reported for the bacterial mutagenicity of these substances in Salmonella typhimurium TA98.

  1. Measurement of particulate phase polycyclic aromatic hydrocarbon (PAHs) around a petroleum refinery.

    PubMed

    Rao, Padma S; Ansari, M Faiyaz; Pipalatkar, P; Kumar, A; Nema, P; Devotta, S

    2008-02-01

    A study on concentrations of ambient particulates viz. total suspended particulate matters (TSP), respirable suspended particulate matter (RSPM) and polycyclic aromatic hydrocarbons (PAH) were carried out at six sites around the Asia's largest, 12 MMTPA, petroleum refinery in west coast of India. PAH concentrations are correlated with each other in these sites, suggesting that they have related sources and sinks. The present article discusses the monitoring aspects such as sample collection, pretreatment and analytical methods and compares the monitored levels for assessing the source receptor distribution pattern. The main sources of RSPM and PAHs in urban air are automobile exhaust (CPCB, Polycyclic aromatic hydrocarbons (PAHs) in air and their effects on human health. " http://www.cpcb.nic.in/ph/ch21103.htm ", 2003; Manuel et al., Environmental Science and Technology, 13: 227-231, 2004) and industrial emissions like petroleum refinery (Vo-Dinh, Chemical analysis of polycyclic aromatic hydrocarbons, Wiley: New York, 1989; Wagrowaski and Hites, Environmental Science and Technology, 31: 279-282, 1997). Polycyclic aromatic hydrocarbons (PAH) are ubiquitous constituents of urban airborne particulate mostly generated by anthropogenic activities (Li et al., Environmental Science and Technology, 37:1958-2965, 2003; Thorsen et al., Environmental Science and Technology, 38: 2029-2037, 2004; Ohura et al., Environmental Science and Technology, 32: 450-455, 2004) and some of them are of major health concern mainly due to their well-known carcinogenic and mutagenic properties (Soclo et al., Marine Pollution Bulletin, 40: 387-396, 2000; Chen et al., Environment International, 28: 659-668, 2003; Larsen and Baker, Environmental Science and Technology, 32: 450-455, 2003). Limited information is available on PAHs contributions from refineries to ambient air. Hence this study would not only create a database but also provide necessary inputs towards dose-response relationship for

  2. Contamination of soils in the urbanized areas of Belarus with polycyclic aromatic hydrocarbons

    NASA Astrophysics Data System (ADS)

    Kukharchyk, T. I.; Khomich, V. S.; Kakareka, S. V.; Kurman, P. V.; Kozyrenko, M. I.

    2013-02-01

    The content of polycyclic aromatic hydrocarbons (PAHs) in the soils of urbanized areas, including the impact zones of Belarus, were studied. The concentrations of 16 PAHs in the soils were determined for individual and high-rise building zones, forests, and forest parks of Belarus. The levels of the PAH accumulation in the soils of different industrial enterprises and boiler stations were analyzed. Possible sources of soil contamination with PAHs were considered, and the structure of the PAHs in the soils was shown. The levels of the soil contamination were determined from the regulated parameters for individual compounds and the sum of 16 PAHs.

  3. Characterization and source apportionment of polycyclic aromatic hydrocarbons (PAHs) in Sediments from the Bohai Sea, China

    NASA Astrophysics Data System (ADS)

    Liu, Jihua; Hu, Ningjing; Shi, Xuefa

    2015-04-01

    Characterization and source apportionment of polycyclic aromatic hydrocarbons (PAHs) in Sediments from the Bohai Sea, China Liu Jihua, Hu Ningjing, Shi Xuefa First Institute of Oceanography, State Oceanic Administration, Qingdao 266061, China Polycyclic aromatic hydrocarbons (PAHs) are a class of ubiquitous organic contaminants in the environment. Indeed, 16 PAH compounds have been listed as priority pollutants by the United States Environmental Protection Agency and the European Union because of their potential toxicity to humans and ecosystems. As POPs are released or escape into the environment, their global accumulation in marine sediments generates a complex balance between inputs and outputs. Furthermore, PAHs in coastal sediments can serve as effective tracers of materials transport from land-to-sea (Fang et al., 2009). Hence, investigations of PAHs in sediments can provide useful information for further understanding of environmental processes and material transport. In this study, sixteen polycyclic aromatic hydrocarbons (PAHs) were extracted from a total of 112 surface sediment samples collected across the entire territory of the Bohai Sea. The detectable concentrations of PAHs ranged from 97.2 to 300.7 ng/g across all samples, indicating low contamination levels of PAHs compared with reported values for other coastal sediments in China and developed countries. The highest concentrations were found within three belts in the vicinity of Luan River Estuary-Qinhuangdao Harbor, the Cao River Estuary-Bohai Sea Center, and north of the Yellow River Estuary. The distribution patterns of PAHs and source identification implied that PAH contamination in the Bohai Sea mainly originates from offshore oil exploration, sewage discharge from rivers and shipping activities. Further Principal components analysis (PCA)/multivariate linear regression (MLR) analysis suggested that the contributions of spilled oil products (petrogenic), coal combustion and traffic

  4. Biotransformation of polycyclic aromatic hydrocarbons by yeasts isolated from coastal sediments

    SciTech Connect

    MacGillivray, A.R.; Shiaris, M.P. )

    1993-05-01

    The environmental significance of fungal transformation of polycyclic aromatic hydrocarbons (PAHs) is of increasing interest. Filamentous fungi and yeast are common in marine environments. However, PAH-degrading marine yeast isolates have not been evaluated for their ability to oxidize PAHs in the presence of alternative carbon sources, though this may be significant in marine environments. In this study phenanthrene and benz[a]anthracese were used as model PAH compounds. The investigation quantified the presence of yeasts in coastal sediments and evaluated their potential to biodegrade PAHs. 50 refs., 4 tabs.

  5. First detection of an ultraviolet transition in an ionized polycyclic aromatic hydrocarbon

    NASA Astrophysics Data System (ADS)

    Chillier, Xavier D. F.; Stone, Bradley M.; Salama, Farid; Allamandola, Louis J.

    1999-07-01

    We report the first measurement of a polycyclic aromatic hydrocarbon cation electronic transition in the ultraviolet spectral region. The UV excitation spectrum of the Dn-XD0 transition of the perylene cation (C20H12+) isolated in an argon matrix was pumped with tunable, coherent radiation and monitored using the vibronic bands of the D1(2B3g)→(2Au)D0 system. The two component band peaks at 244 and 250.2 nm, close to the S2(1B3u)←(1Ag)S0 transition in neutral perylene.

  6. Low band gap polycyclic hydrocarbons: from closed-shell near infrared dyes and semiconductors to open-shell radicals.

    PubMed

    Sun, Zhe; Ye, Qun; Chi, Chunyan; Wu, Jishan

    2012-12-07

    Low band gap (E(g) < 1.5 eV) polycyclic hydrocarbons have become one of the most important types of materials for many applications, for example, as semiconductors in organic field effect transistors (OFETs), as light-harvesting dyes in organic solar cells and photodetectors, as near infrared (NIR) fluorescent probes in high resolution bio-imaging and bio-sensing, and as chromophores in non-linear optics. The benzenoid polycyclic hydrocarbons as nano-sized graphene fragments also serve as perfect model compounds to understand the fundamental structure-property relationship of graphene. The ground state of these molecules can be described as either a closed-shell or an open-shell structure on the basis of their molecular size and edge structure. In this review, a summary will be given on a series of low band gap polycyclic hydrocarbons about their synthesis, physical properties and material applications.

  7. THE EFFECT OF ROUTE OF ADMINISTRATION OF POLYCYCLIC AROMATIC HYDROCARBONS ON DNA ADDUCTION AND CYTOGENETIC DAMAGE IN PERIPHERAL BLOOD LYMPHOCYTES OF MICE AND RATS

    EPA Science Inventory

    The effect of route of administration of polycyclic aromatic hydrocarbons on DNA adduction and cytogenetic damage in peripheral blood lymphocytes of mice and rats

    Experiments were designed to investigate how the route of exposure to polycyclic
    aromatic hydrocarbons (PA...

  8. Effects of co-occurring aromatic hydrocarbons on degradation of individual polycyclic aromatic hydrocarbons in marine sediment slurries

    SciTech Connect

    Bauer, J.E.; Capone, D.G.

    1988-07-01

    Rates of polycyclic aromatic hydrocarbon (PAH) degradation and mineralization were influenced by preexposure to alternate PAHs and a monoaromatic hydrocarbon at relatively high (100 ppm) concentrations in organic-rich aerobic marine sediments. Prior exposure to three PAHs and benzene resulted in enhanced (/sup 14/C)naphthalene mineralization, while (/sup 14/C)anthracene mineralization was stimulated only by benzene and anthracene preexposure. Preexposure of sediment slurries to phenanthrene stimulated the initial degradation of anthracene. Prior exposure to naphthalene stimulated the initial degradation of phenanthrene but had no effect on either the initial degradation of mineralization of anthracene. For those compounds which stimulated (/sup 14/C)anthracene of (/sup 14/C)naphthalene mineralization, longer preexposures (2 weeks) to alternative aromatic hydrocarbons resulted in an even greater stimulation response. Enrichment with individual PAHs followed by subsequent incubation with one or two PAHs showed no alteration in degradation patterns due to the simultaneous presence of PAHs. The evidence suggests that exposure of marine sediments to a particular PAH or benzene results in the enhanced ability of these sediments to subsequently degrade that PAH as well as certain other PAHs. The enhanced degradation of a particular PAH after sediments have been exposed to it may result from the selection and proliferation of specific microbial populations capable of degrading it.

  9. Comparison of supercritical fluid extraction and Soxhlet extraction for the determination of aliphatic hydrocarbons in seaweed samples.

    PubMed

    Punín Crespo, M O; Lage Yusty, M A

    2006-07-01

    Supercritical fluid extraction (SFE) and Soxhlet extraction methods were compared in a study of the aliphatic hydrocarbon profiles of seaweed samples. Method precision for Soxhlet extraction (< or = 7.58%) was slightly better than that for SFE (< or = 9.28%) except for C28. The SFE method is a good alternative for the routine determination of alkanes in seaweed samples; however, for a complete study of shorter-chain n-alkanes, the Soxhlet extraction is a more suitable method. To evaluate the SFE and Soxhlet methods developed, three diverse Undaria pinnatifida samples collected at different dates and areas of the Galician coast were analyzed. n-Alkanes C18, C20, C22, C24, and C28 were found in all samples, with values lower than 7.9 microg g(-1) d.w. The total hydrocarbon content was within the range of 13.6-21.7 microg g(-1) d.w. C18 was found to be the most abundant.

  10. Degradation of polycyclic aromatic hydrocarbons in the presence of synthetic surfactants

    SciTech Connect

    Tiehm, A. )

    1994-01-01

    The biodegradation of polycyclic aromatic hydrocarbons (PAH) often is limited by low water solubility and dissolution rate. Nonionic surfactants and sodium dodecyl sulfate increased the concentration of PAH in the water phase because of solubilization. The degradation of PAH was inhibited by sodium dodecyl sulfate because this surfactant was preferred as a growth substrate. Growth of mixed cultures with phenanthrene and fluroanthrene solubilized by a nonionic surfactant prior to inoculation was exponential, indicating a high bioavailability of the solubilized hydrocarbons. Nonionic surfactants of the alkylethoxylate type and the alkylphenolethoxylate type with an average ethoxylate chain length of 9 to 12 monomers were toxic to a PAH-degrading Mycobacterium sp. and to several PAH-degrading mixed cultures. Toxicity of the surfactants decreased with increasing hydrophilicity, i.e., with increasing ethoxylate chain length. Nontoxic surfactants enhanced the degradation of fluorene, phenanthrene, anthracene, fluoranthene, and pyrene.

  11. Analysis of the impregnation of ZnO:Mn2+ nanoparticles on cigarette filters for trapping polycyclic aromatic hydrocarbons (PAHs)

    NASA Astrophysics Data System (ADS)

    Estrada-Izquierdo, Irma; Sánchez-Espindola, Esther; Uribe-Hernández, Raúl; Ramón-Gallegos, Eva

    2012-10-01

    Each cigarette can generate 1149 ng of a mixture of 14 polycyclic aromatic hydrocarbons, of which there are a lot of information about its harmful effects on the environment and human health, they are considered mutagenic, teratogenic and carcinogenic. In this paper we tested ZnO:Mn2+ nanoparticles, attached to the filters of cigarettes. The first results showed that the filtration system was able to catch the Benzo(a)pyrene contained in cigarette smoke; but more tests are needed to quantify the efficiency with greater accuracy over other polycyclic aromatic hydrocarbons.

  12. Processing of atmospheric polycyclic aromatic hydrocarbons by fog in an urban environment.

    PubMed

    Ehrenhauser, Franz S; Khadapkar, Kalindi; Wang, Youliang; Hutchings, James W; Delhomme, Olivier; Kommalapati, Raghava R; Herckes, Pierre; Wornat, Mary J; Valsaraj, Kalliat T

    2012-10-26

    Polycyclic aromatic hydrocarbons (PAH) are ubiquitous pollutants in the atmosphere, predominantly known for their toxicity. Although there has been substantial work on the atmospheric degradation of PAH, little is known about how the presence of atmospheric droplets (e.g., a fog cloud) affects the fate of PAH. In order to assess the processing of PAH and their corresponding oxidation products during a fog event, two field-sampling campaigns in Fresno, CA and Davis, CA were conducted. The simultaneous evaluation of concentrations of the PAH and oxygenated polycyclic aromatic compounds (OPAC) in the gas phase, particulate matter and fog water droplets before, during and after fog allows for the characterization of transformative and transport processes in a fog cloud. By tracking the ratio of OPAC to PAH in the individual atmospheric phases, two major polycyclic aromatic compounds-processing pathways can be identified: (i) the dissolution of OPAC from particulate matter and (ii) the uptake and oxidation of PAH in the fog water droplets. Wet deposition steadily decreases the pollutant concentration in the fog cloud droplets during a fog event; however, uptake and concentration via evaporative water loss upon the dissipation of a fog cloud cause an increase in the atmospheric pollutant concentration.

  13. Polycyclic Aromatic Hydrocarbons (PAHs) in urban atmospheric particulate of NCR, Delhi, India

    NASA Astrophysics Data System (ADS)

    Sonwani, Saurabh; Amreen, Hassan; Khillare, P. S.

    2016-07-01

    The present study identifies the particulate Polycyclic Aromatic hydrocarbons (PAHs) and their sources in ambient atmosphere of Delhi, India. PM10 (aerodynamic diameter, ≤10 μm) samples were collected weekly at two residential areas from July 2013 to January 2014. First sampling site was located in centre of the city, while other was at city's background (located in South-East direction of the Delhi). PM10 was collected on Whatman GF/A (8"x10") glass fibre filters using High-Volume sampler having a constant flow rate of 1.10 m3/min. A total of 55 samples, 27 from city centre and 28 from background site were collected during sampling period, covering two different seasons. The samples were analysed for determination of 16 Polycyclic Aromatic Hydrocarbons by using High Performance Liquid Chromatography (HPLC) system (Waters, USA). A source apportionment study using Molecular Diagnostic Ratio (MDR) and Principal Component Analysis (PCA) were conducted for both sampling sites in order to identify the potential PAHs sources in Delhi. MDR was used for the preliminary identification of sources and PCA was used for further confirmation of the PAH sources at both the sites in Delhi. Results indicated towards traffic and coal combustion related sources as dominant contributors of urban atmospheric PAHs in Delhi.

  14. Polycyclic aromatic hydrocarbon-DNA adducts and the CYP1A1 restriction fragment length polymorphism

    SciTech Connect

    Shields, P.G.; Bowman, E.D.; Weston, A.; Harris, C.C.; Sugimura, H.; Caporaso, N.E.; Petruzzelli, S.F. ); Trump, B.F. )

    1992-11-01

    Human cancer risk assessment at a genetic level involves the investigation of carcinogen metabolism and DNA adduct formation. Wide interindividual differences in metabolism result in different DNA adduct levels. For this and other reasons, many laboratories have considered DNA adducts to be a measure of the biologically effective dose of a carcinogen. Techniques for studying DNA adducts using chemically specific assays are becoming available. A modification of the [sup 32]P-postlabeling assay for polycyclic aromatic hydrocarbon DNA adducts described here provides potential improvements in quantification. DNA adducts, however, reflect only recent exposure to carcinogens; in contrast, genetic testing for metabolic capacity indicates the extent to which carcinogens can be activated and exert genotoxic effects. Such studies may reflect both separate and integrated risk factors together with DNA adduct levels. A recently described restriction fragment length polymorphism for the CYP1A1, which codes for the cytochrome P450 enzyme primarily responsible for the metabolic activation of carcinogenic polycyclic aromatic hydrocarbons, has been found to be associated with lung cancer risk in a Japanese population. In a subset of individuals enrolled in a US lung cancer case-control study, no association with lung cancer was found. 17 refs., 3 figs.

  15. Gene biomarkers in diatom Thalassiosira pseudonana exposed to polycyclic aromatic hydrocarbons from contaminated marine surface sediments.

    PubMed

    Carvalho, Raquel N; Burchardt, Alina D; Sena, Fabrizio; Mariani, Giulio; Mueller, Anne; Bopp, Stephanie K; Umlauf, Gunther; Lettieri, Teresa

    2011-01-17

    Marine diatoms have a key role in the global carbon fixation and therefore in the ecosystem. We used Thalassiosira pseudonana as a model organism to assess the effects of exposure to environmental pollutants at the gene expression level. Diatoms were exposed to polycyclic aromatic hydrocarbons mixture (PAH) from surface sediments collected at a highly PAH contaminated area of the Mediterranean Sea (Genoa, Italy), due to intense industrial and harbor activities. The gene expression data for exposure to the sediment-derived PAH mixture was compared with gene expression data for in vitro exposure to specific polycyclic aromatic hydrocarbons. The data shows that genes involved in stress response, silica uptake, and metabolism were regulated both upon exposure to the sediment-derived PAH mixture and to the single component. Complementary monitoring of silica in the diatom cultures provide further evidence of a reduced cellular uptake of silica as an end-point for benzo[a]pyrene exposure that could be linked with the reduced gene and protein expression of the silicon transporter protein. However some genes showed differences in regulation indicating that mixtures of structurally related chemical compounds can elicit a slightly different gene expression response compared to that of a single component. The paper provides indications on the specific pathways affected by PAH exposure and shows that selected genes (silicon transporter, and silaffin 3) involved in silica uptake and metabolism could be suitable molecular biomarkers of exposure to PAHs.

  16. Firefighting instructors' exposures to polycyclic aromatic hydrocarbons during live fire training scenarios.

    PubMed

    Kirk, Katherine M; Logan, Michael B

    2015-01-01

    Cumulative exposures of firefighting instructors to toxic contaminants generated from live-fire training potentially far exceed firefighter exposures arising from operational fires. This study measured the atmospheric concentrations of polycyclic aromatic hydrocarbons (PAHs) outside and inside the structural firefighting ensembles worn by instructors during five live fire training evolutions. In addition, the contamination of ensembles by deposition of PAHs was characterized. Concentrations of polycyclic aromatic hydrocarbons outside the instructors' structural firefighting ensembles during the training evolutions ranged from 430 μg/m(3) to 2700 μg/m(3), and inside the structural firefighting ensembles from 32 μg/m(3) to 355 μg/m(3). Naphthalene, phenanthrene and acenaphthylene dominated the PAHs generated in the live fire evolutions, but benzo[a]pyrene was the greatest contributor to the toxicity of the PAH mixture both inside and outside the structural firefighting ensembles. Deposition of PAHs onto the structural firefighting ensembles was measured at between 69 and 290 ng/cm(2), with phenanthrene, fluoranthene, pyrene, and benzo[a]anthracene detected on all samples. These findings suggest that firefighting instructor exposures to PAHs during a single live-fire training evolution are comparable with exposures occurring in industrial settings over a full shift. Further research is required to investigate the importance of various potential routes of exposure to PAHs as a result of ingress and deposition of PAHs in/on structural firefighting ensembles.

  17. CYP63A2, a catalytically versatile fungal P450 monooxygenase capable of oxidizing higher-molecular-weight polycyclic aromatic hydrocarbons, alkylphenols, and alkanes.

    PubMed

    Syed, Khajamohiddin; Porollo, Aleksey; Lam, Ying Wai; Grimmett, Paul E; Yadav, Jagjit S

    2013-04-01

    Cytochrome P450 monooxygenases (P450s) are known to oxidize hydrocarbons, albeit with limited substrate specificity across classes of these compounds. Here we report a P450 monooxygenase (CYP63A2) from the model ligninolytic white rot fungus Phanerochaete chrysosporium that was found to possess a broad oxidizing capability toward structurally diverse hydrocarbons belonging to mutagenic/carcinogenic fused-ring higher-molecular-weight polycyclic aromatic hydrocarbons (HMW-PAHs), endocrine-disrupting long-chain alkylphenols (APs), and crude oil aliphatic hydrocarbon n-alkanes. A homology-based three-dimensional (3D) model revealed the presence of an extraordinarily large active-site cavity in CYP63A2 compared to the mammalian PAH-oxidizing (CYP3A4, CYP1A2, and CYP1B1) and bacterial aliphatic-hydrocarbon-oxidizing (CYP101D and CYP102A1) P450s. This structural feature in conjunction with ligand docking simulations suggested potential versatility of the enzyme. Experimental characterization using recombinantly expressed CYP63A2 revealed its ability to oxidize HMW-PAHs of various ring sizes, including 4 rings (pyrene and fluoranthene), 5 rings [benzo(a)pyrene], and 6 rings [benzo(ghi)perylene], with the highest enzymatic activity being toward the 5-ring PAH followed by the 4-ring and 6-ring PAHs, in that order. Recombinant CYP63A2 activity yielded monohydroxylated PAH metabolites. The enzyme was found to also act as an alkane ω-hydroxylase that oxidized n-alkanes with various chain lengths (C9 to C12 and C15 to C19), as well as alkyl side chains (C3 to C9) in alkylphenols (APs). CYP63A2 showed preferential oxidation of long-chain APs and alkanes. To our knowledge, this is the first P450 identified from any of the biological kingdoms that possesses such broad substrate specificity toward structurally diverse xenobiotics (PAHs, APs, and alkanes), making it a potent enzyme biocatalyst candidate to handle mixed pollution (e.g., crude oil spills).

  18. Determination of total and polycyclic aromatic hydrocarbons in aviation jet fuel.

    PubMed

    Bernabei, M; Reda, R; Galiero, R; Bocchinfuso, G

    2003-01-24

    The aviation jet fuel widely used in turbine engine aircraft is manufactured from straight-run kerosene. The combustion quality of jet fuel is largely related to the hydrocarbon composition of the fuel itself; paraffins have better burning properties than aromatic compounds, especially naphthalenes and light polycyclic aromatic hydrocarbons (PAHs), which are characterised as soot and smoke producers. For this reason the burning quality of fuel is generally measured as smoke fermation. This evaluation is carried out with UV spectrophotometric determination of total naphthalene hydrocarbons and a chromatographic analysis to determine the total aromatic compounds. These methods can be considered insufficient to evaluate the human health impact of these compounds due to their inability to measure trace (ppm) amounts of each aromatic hyrcarbon and each PAH in accordance with limitations imposed because of their toxicological properties. In this paper two analytical methods are presented. Both are based on a gas chromatographic technique with a mass detector operating in be selected ion monitoring mode. The first method was able to determine more than 60 aromatic hydrocarbons in a fuel sample in a 35-min chromatographic run, while the second was able to carry out the analysis of more than 30 PAHs in a 40-min chromatographic run. The linearity and sensitivity of the methods in measuring these analytes at trace levels are described.

  19. Distribution and fate of aliphatic and aromatic hydrocarbons in Antarctic fauna and environment

    NASA Astrophysics Data System (ADS)

    Platt, H. M.; Mackie, P. R.

    1980-03-01

    With the depletion of oil resources in more accessible areas, those of remote regions are being considered or indeed are now being exploited. In many of these regions, especially the polar ones, little is known of the effects such exploitation will have on the environment. But it is known that the ecosystems are often subject to great stress by natural climatic conditions and additional burdens imposed by man may have catastrophic environmental effects. South Georgia, a sub-Antarctic island, has a history of industrial activity mainly concerned with whaling operations that peaked around 1925-1935 but has since declined to virtually nothing. Studies of the ecology of the area provided a unique opportunity to assess the long-term effects that such activities had on the ecosystem. Off the whaling stations a considerable amount of waste material, including fuel oil, was released into the bays and inevitably some of this material was deposited in the sediments. Chemical evidence in the form of both paraffinic and aromatic hydrocarbons still persists in the sediments. The implications of this persistence in relation to the possible influence of the low temperature conditions are discussed. The superficial sediments, marine biota and terrestrial plants, which since 1965 have returned virtually to a pristine state, contain hydrocarbons essentially similar to unpolluted areas around the coast of Britain. Relatively high levels of carcinogenic/mutagenic polynuclear aromatic hydrocarbons in surface sediments suggests a world-wide background of abiogenic hydrocarbons probably disseminated by airborne transport. This appears to indicate that contamination reaches even remote parts of the world in relatively undiminished quantities.

  20. Atmospheric behaviors of particulate-bound polycyclic aromatic hydrocarbons and nitropolycyclic aromatic hydrocarbons in Beijing, China from 2004 to 2010

    NASA Astrophysics Data System (ADS)

    Tang, Ning; Suzuki, Genki; Morisaki, Hiroshi; Tokuda, Takahiro; Yang, Xiaoyang; Zhao, Lixia; Lin, Jinming; Kameda, Takayuki; Toriba, Akira; Hayakawa, Kazuichi

    2017-03-01

    Airborne particulates were collected at an urban site (site 1) from 2004 to 2010 and at a suburban site (site 2) in 2010 in Beijing. Nine polycyclic aromatic hydrocarbons (PAHs) and five nitropolycyclic aromatic hydrocarbons (NPAHs) in the airborne particulates were determined by HPLC with fluorescence and chemiluminescence detection, respectively. The concentrations of PAHs and NPAHs were higher in heating season than in non-heating season at the two sites. Both the concentrations of PAHs and NPAHs decreased in the non-heating season but only the concentrations of NPAHs decreased in heating season at site 1, from 2004 to 2010. These findings suggest that source control measures implemented by the city of Beijing helped to reduce air pollution in Beijing. The concentrations of PAHs increased at site 1 in 2010, possibly because of the transport of emissions from windward other areas, such as Shanxi province. Several diagnostic ratios of PAHs and NPAHs showed that the different sources contributed to Beijing's air pollution, although coal combustion was the main source in the heating season and vehicle emission was the main source in the non-heating season. An analysis of physical parameters at Beijing showed that high wind speed can remove atmospheric PAHs and NPAHs in the heating season and that high relative humidity can remove them in the non-heating season.

  1. Comparison of polycyclic aromatic hydrocarbons and nitropolycyclic aromatic hydrocarbons in airborne particulates collected in downtown and suburban Kanazawa, Japan

    NASA Astrophysics Data System (ADS)

    Hayakawa, Kazuichi; Tang, Ning; Akutsu, Kazuhiko; Murahashi, Tsuyoshi; Kakimoto, Hitoshi; Kizu, Ryoichi; Toriba, Akira

    In this study, airborne particulates were collected at three sites, two in a downtown area and the other in a suburban area of Kanazawa, Japan in each season for 7 years. Two polycyclic aromatic hydrocarbons (PAHs), pyrene (Py) and benzo[ a]pyrene (BaP) and four nitropolycyclic aromatic hydrocarbons (NPAHs), 1-nitropyrene (NP) and 1,3-, 1,6-, and 1,8-dinitropyrenes (DNP) were determined by high-performance liquid chromatography with fluorescence and chemiluminescence detection. At the downtown sites, the mean concentration of each DNP was about two orders of magnitude lower than that of 1-NP and more than three orders of magnitude lower than those of Py and BaP. This tendency reflected the composition of PAHs and NPAHs in diesel-engine exhaust particulates. Concentrations of these PAHs and NPAHs were higher at the downtown sites than at the suburban site, suggesting the dilution of these compounds during the transportation from the downtown to the suburban area. The concentration ratios of NPAHs to PAHs were larger at the downtown sites than at the suburban site. Studies using UV light and sunlight showed that degradation of NPAHs was faster than that of PAHs. Thus, the lower concentrations of NPAHs in the suburban sites may be due to their being photodegraded faster than PAHs during the atmospheric transportation from the downtown area to the suburban area.

  2. Formation of soot from polycyclic aromatic hydrocarbons as well as fullerenes and carbon nanotubes in the combustion of hydrocarbon

    NASA Astrophysics Data System (ADS)

    Mansurov, Z. A.

    2011-01-01

    The eightieth anniversary of Academician, Lenin Prize Winner Rem Ivanovich Soloukhin is an important event for the scientific association of investigators of combustion and detonation processes. R. I. Soloukhin has developed original gasdynamic laser systems based on the selective thermal excitation and mixing in a supersonic flow: efficient high-power gas-flow lasers of convective type with electric excitation and chemical lasers initiated by an electron beam. He proposed methods of measuring the rapidly changing pressure, density, temperature, and other parameters of processes occurring in shock waves. Deputy Editor-in-Chief of the Journal "Fizika Goreniya Vzryva," Professor at Novosibirsk University R. I. Soloukhin trained a Pleiad of Doctors and Candidates of Sciences. His fundamental investigations form the basis for the development of new directions in the physics of combustion and explosion. In the present article, recent works on soot formation in the combustion of hydrocarbons are reviewed. The phenomenology, kinetics, and mechanism of soot formation, the influence of different factors on the formation of polycyclic aromatic hydrocarbons, fullerenes, carbon nanotubes, and soot, low-temperature cold-flame soot formation, the combustion in an electric field, and the paramagnetism of soot particles were considered from the environmental standpoint.

  3. Distribution and risk assessment of hydrocarbons (aliphatic and PAHs), polychlorinated biphenyls (PCBs), and pesticides in surface sediments from an agricultural river (Durance) and an industrialized urban lagoon (Berre lagoon), France.

    PubMed

    Kanzari, Fehmi; Asia, Laurence; Syakti, Agung Dhamar; Piram, Anne; Malleret, Laure; Mille, Gilbert; Doumenq, Pierre

    2015-09-01

    The distributions of organic pollutants (like hydrocarbons, polychlorinated biphenyls (PCBs), and pesticides) and the risks on the ecosystem were studied in the Durance River and the Berre lagoon (France). High levels of aliphatic hydrocarbons were observed in all stations (1399 to 11,202 μg kg(-1) dw). The n-alkanes were mainly from terrigenous origin confirmed by the values of different ratios calculated (carbon preference index (CPI), natural n-alkanes ratio (NAR), terrigenous/aquatic ratio (TAR), and ratio of low molecular weight to high molecular weight (LMW/HMW)). Total polycyclic aromatic hydrocarbon (PAH) concentrations in the surface sediments of the Durance River and Berre lagoon are 57-1528 and 512-863 μg kg(-1) dw, respectively. Several ratios between parent polycyclic aromatic hydrocarbons showed that the sources of hydrocarbons in the sediments were generally more pyrolytic than petrogenic. The sum of seven PCB contents ranged from 0.03 to 13.13 μg kg(-1) dw. Higher levels of PCBs were detected in sediments from the northern parts of the Berre lagoon (stations B1 and B3). Total pesticides contents ranged from 0.02 to 7.15 μg kg(-1) dw. Among these compounds, ∑DDE and ∑DDT contents ranged, respectively, from 0.35 to 1.65 and from 0.37 to 1.52 μg kg(-1) dw. However, PAH and PCB levels are not high enough to be a threat to aquatic organisms and human beings. Total PAH levels were below the effects range low (ERL) of 3500 μg kg(-1) dw. For PCBs, only two stations (B1 and B3) are higher than the effect range median (ERM) of 180 μg kg(-1) dw. For endrin (pesticide), the concentrations are between the ERL (0.02 μg kg(-1) dw) and the ERM (45 μg kg(-1) dw).

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

    NASA Astrophysics Data System (ADS)

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

    2015-02-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2014-10-01

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

  6. In vitro toxicity of polycyclic aromatic hydrocarbons and halogenated aromatic hydrocarbons to cetacean cells and tissues

    SciTech Connect

    Carvan, M.J. III.

    1993-01-01

    Cetaceans bioaccumulate high aromatic hydrocarbon tissue residues, and elevated levels of PCB residues in tissues are proposed to have occurred concurrently with recent epizootic deaths of dolphins. The objectives of this study were: (1) to develop and characterize an epithelial cell line derived from dolphin tissues, (2) to investigate the effects of hydrocarbon pollutants on those cells, and (3) to analyze the toxicity of hydrocarbon pollutants on cetacean tissues in vitro. An epithelial cell line, Carvan dolphin kidney (CDK), isolated from a spontaneously aborted female bottlenose dolphin, Tursiops truncatus, grew rapidly. These cells were neither transformed nor immortal. Velocity sedimentation analysis showed CDK cells contained nuclear aryl hydrocarbon receptor, suggestive of cytochrome P450 inducibility. BaP inhibited mitosis in CDK cells in a dose-dependent manner. Data indicate that CDK cells metabolize BaP, that BaP metabolites bind to cellular DNA initiating unscheduled DNA synthesis, and that the inhibition of cytochrome P450 metabolism decrease the BaP-associated inhibition of mitosis in dolphin cells. The data also suggest that TCDD acts synergistically to increase the levels of DNA damage by the procarcinogen BaP. Cetacean liver microsomes was isolated and evaluated for the presence of cytochrome P450 proteins by SDS-PAGE, apparent minimum molecular weight determination, and immunoblot analysis. P450 activity was induced in cetacean tissue samples and CDK cells by exposure in vitro to one of several cytochrome P450-inducing chemicals. The data suggest that cetacean tissues and cells can be utilized to study the in vitro induction of cytochrome P450, resultant metabolism of xenobiotic contaminants, and the subsequent cellular and molecular responses. However, the identity of specific P450 isozymes involved in this process will remain undetermined until monoclonal antibodies that recognize cetacean P450s can be generated.

  7. LASER DESORPTION-IONIZATION OF POLYCYCLIC AROMATIC HYDROCARBONS FROM GLASS SURFACES WITH ION MOBILITY SPECTROMETRY ANALYSIS. (R826769)

    EPA Science Inventory

    Polycyclic aromatic hydrocarbons (PAHs) were analyzed as adsorbates on borosilicate glass at levels from 40 pg (5.5 pg mm-2) to 7 small mu, Greekg (1 

  8. Determination of polycyclic aromatic hydrocarbons by four-way parallel factor analysis in presence of humic acid

    NASA Astrophysics Data System (ADS)

    Yang, Ruifang; Zhao, Nanjing; Xiao, Xue; Yu, Shaohui; Liu, Jianguo; Liu, Wenqing

    2016-01-01

    There is not effective method to solve the quenching effect of quencher in fluorescence spectra measurement and recognition of polycyclic aromatic hydrocarbons in aquatic environment. In this work, a four-way dataset combined with four-way parallel factor analysis is used to identify and quantify polycyclic aromatic hydrocarbons in the presence of humic acid, a fluorescent quencher and an ubiquitous substance in aquatic system, through modeling the quenching effect of humic acid by decomposing the four-way dataset into four loading matrices corresponding to relative concentration, excitation spectra, emission spectra and fluorescence quantum yield, respectively. It is found that Phenanthrene, pyrene, anthracene and fluorene can be recognized simultaneously with the similarities all above 0.980 between resolved spectra and reference spectra. Moreover, the concentrations of them ranging from 0 to 8 μg L-1 in the test samples prepared with river water could also be predicted successfully with recovery rate of each polycyclic aromatic hydrocarbon between 100% and 120%, which were higher than those of three-way PARAFAC. These results demonstrate that the combination of four-way dataset with four-way parallel factor analysis could be a promising method to recognize the fluorescence spectra of polycyclic aromatic hydrocarbons in the presence of fluorescent quencher from both qualitative and quantitative perspective.

  9. Draft Genome Sequence of Halotolerant Polycyclic Aromatic Hydrocarbon-Degrading Pseudomonas bauzanensis Strain W13Z2

    PubMed Central

    Jin, Decai; Zhou, Lisha; Wu, Liang; Qi, Lin; Li, Chen; An, Wei; Chen, Yu

    2014-01-01

    Pseudomonas bauzanensis W13Z2 is a halotolerant polycyclic aromatic hydrocarbon (PAH)-degrading bacterium isolated from petroleum-contaminated drill cuttings in the Bohai Sea. Here, we report the 8.6-Mb draft genome sequence of this strain, which will provide insights into the diversity of Pseudomonas and the mechanism of PAHs degradation in drill cuttings. PMID:25323719

  10. PILOT-SCALE SUBCRITICAL WATER REMEDIATION OF POLYCYCLIC AROMATIC HYDROCARBON- AND PESTICIDE-CONTAMINATED SOIL. (R825394)

    EPA Science Inventory

    Subcritical water (hot water under enough pressure to maintain the liquid
    state) was used to remove polycyclic aromatic hydrocarbons (PAHs) and pesticides
    from highly contaminated soils. Laboratory-scale (8 g of soil) experiments were
    used to determine conditions f...

  11. Cumulative Exposure Assessment for Trace-Level Polycyclic Aromatic Hydrocarbons (PAHs) using Human Blood and Plasma Analysis

    EPA Science Inventory

    Humans experience chronic cumulative trace-level exposure to mixtures of volatile, semi-volatile, and non-volatile polycyclic aromatic hydrocarbons (PAHs) present in the environment as by-products of combustion processes. Certain PAHs are known or suspected human carcinogens and ...

  12. Development of a Relative Potency Factor (Rpf) Approach for Polycyclic Aromatic Hydrocarbon (PAH) Mixtures (External Review Draft)

    EPA Science Inventory

    EPA is conducting a peer review and public comment of the scientific basis supporting the human health hazard and dose-response assessment of polycyclic aromatic hydrocarbon (PAH) mixtures that when finalized will appear on the Integrated Risk Information System (IRIS) database. ...

  13. THE EFFECTS OF EQUIVALENCE RATIO ON THE FORMATION OF POLYCYCLIC AROMATIC HYDROCARBONS AND SOOT IN PREMIXED ETHANE FLAMES. (R825412)

    EPA Science Inventory

    Abstract

    The formation of polycyclic aromatic hydrocarbons (PAH) and soot has been investigated in atmospheric-pressure, laminar, ethane/oxygen/argon premixed flames as a function of mixture equivalence ratio. Mole fraction profiles of major products, trace aromatics, ...

  14. CYCLOPENTA-FUSED POLYCYCLIC AROMATIC HYDROCARBONS IN STRAIN A/J MOUSE LUNG: DNA ADDUCTS, ONCOGENE MUTATIONS, & TUMORIGENESIS

    EPA Science Inventory

    Cyclopenta-fused Polycyclic Aromatic Hydrocarbons in Strain AJJ Mouse Lung: DNA Adducts, Oncogene Mutations, and Tumorigenesis.

    We have examined the relationships between DNA adducts, Ki-ras oncogene mutations, DNA adducts, and adenoma induction in the lungs of strain A/J...

  15. ROLE OF SOURCE MATRIX IN THE BIOAVAILABILITY OF POLYCYCLIC AROMATIC HYDROCARBONS TO DEPOSIT-FEEDING BENTHIC INVERTEBRATES

    EPA Science Inventory

    The bioavailability of polycyclic aromatic hydrocarbons (PAHs) to benthic organisms is complicated by the variety of ways that they are introduced to coastal waters (dissolved, as nonaqueous phase liquids, and tightly bound to soot, coal, tire rubber, and eroded shale). In order ...

  16. TRENDS OF POLYCYCLIC AROMATIC HYDROCARBON LEVELS AND MUTAGENICITY IN SANTIAGO'S INHALABLE AIRBORNE PARTICLES IN THE PERIOD 1992-1996.

    EPA Science Inventory

    Abstract

    Trends of polycyclic aromatic hydrocarbons (PAHs) for 1992-1996 (cold season) and their mutagenic activity were investigated in organic extracts from the Santiago. Chile. inhalable particles (PM10). The highest PAH concentrations were observed in 1992 and decline...

  17. PHOTO-INDUCED POLYCYCLIC AROMATIC HYDROCARBON TOXIC POTENTIALS OF NEAR SHORE LARVAL FISH HABITAT IN THE GREAT LAKES, USA

    EPA Science Inventory

    Photo-induced toxicity (PIT) of polycyclic aromatic hydrocarbons (PAH) has been documented in laboratory studies for both invertebrate and vertebrate aquatic organisms. PIT has not been verified in field studies for larval fish to date. Filtered water samples and larval fish were...

  18. IMPACTS OF AGING ON IN VIVO AND IN VITRO MEASUREMENTS OF SOIL-BOUND POLYCYCLIC AROMATIC HYDROCARBON AVAILABILITY

    EPA Science Inventory

    Ingestion of contaminated soil is an exposure pathway at approximately one-half of the Superfund sites in the United States. This study was designed to evaluate the impacts of aging in soil on the availability of polycyclic aromatic hydrocarbons (PAHs). Two coal tar (CT)-amended ...

  19. [Tobacco smoking as a source of exposure of pregnant women and newborn on polycyclic aromatic hydrocarbons].

    PubMed

    Piekoszewski, Wojciech; Florek, Ewa; Breborowicz, Grzegorz H

    2006-01-01

    An essential problem related to tobacco smoking is exposure of children in the foetal period and early childhood to toxic compounds. The aim of this paper was to assess the exposure of pregnant women and their newborns to polycyclic aromatic hydrocarbons as a consequence of tobacco smoking. The exposure to tobacco smoke was determined through surveys and cotinine measurement in the urine of pregnant women and newborns, and the exposure to polycyclic aromatic hydrocarbons has been determined by measure of 1-hydroxypyrene in the same biological material. The cotinine concentration in the urine of smoking women and their newborns was respectively 416.0 +/- 319.9 ng/mg of creatinine and 46.5 +/- 37.2 ng/mg of creatinine. In case of non-smoking as well as non-exposed patients and their newborns, the concentration of cotinine was 0. The correlation between the concentration of cotinine in the urine of smoking women and their newborns was shown. The mean concentration of 1-hydroxypyrene in the urine of smoking patients was 0.65 +/- 0.45 ng/mg of creatinine, whereas in the urine of newborns, it was 0.46 +/- 0.41 ng/mg of creatinine. The concentration of 1-hydroxypyrene in the urine of smokers was increased together with the increase of cotinine, and the correlation factor was 0.5128. Such dependence was not indicated for concentrations of these compounds in the urine of newborns of these women. Within the group of non-smoking women, the concentration of 1-hydroxypyene urine of women was 0.25 +/- 0.29 ng/mg of creatinine, whereas among children 0.20 +/- 0.23 ng/mg of creatinine. In both examined group (smoking and non-smoking women) there is a dependence between the concentration of 1-hydroxypyrene in the urine of women and their newborns. The research concerning the assessment of exposure of pregnant women and their newborns to polycyclic aromatic hydrocarbons was conducted, and at the same time it was proven, that the placenta does not constitute a barrier for these

  20. Quantification of 16 polycyclic aromatic hydrocarbons in cigarette smoke condensate using stable isotope dilution liquid chromatography with atmospheric-pressure photoionization tandem mass spectrometry.

    PubMed

    Zhang, Xiaotao; Hou, Hongwei; Chen, Huan; Liu, Yong; Wang, An; Hu, Qingyuan

    2015-09-17

    A stable isotope dilution liquid chromatography with tandem mass spectrometry method for the analysis of 16 polycyclic aromatic hydrocarbons in cigarette smoke condensate was developed and validated. Compared with previously reported methods, this method has lower limits of detection (0.04-1.35 ng/cig). Additionally, the proposed method saves time, reduces the number of separation steps, and reduces the quantity of solvent needed. The new method was applied to evaluate polycyclic aromatic hydrocarbon content in 213 commercially available cigarettes in China, under the International Standardization Organization smoking regime and the Health Canadian intense smoking regime. The results showed that the total polycyclic aromatic hydrocarbon content was more than two times higher in samples from the Health Canadian intense smoking regime than in samples from the International Standardization Organization smoking regime (1189.23 vs. 2859.50 ng/cig, p<0.05). Meanwhile, the concentration of individual polycyclic aromatic hydrocarbons (and total polycyclic aromatic hydrocarbons) increased with labeled tar content in both of the tested smoking regimes. There was a positive correlation between total polycyclic aromatic hydrocarbons under the International Standardization Organization smoking regime with that under the Health Canadian intense smoking regime. The proposed liquid chromatography with tandem mass spectrometry method is satisfactory for the rapid, sensitive, and accurately quantitative evaluation of polycyclic aromatic hydrocarbon content in cigarette smoke condensate, and it can be applied to assess potential health risks from smoking. This article is protected by copyright. All rights reserved.

  1. Reaction Dynamics in Astrochemistry: Low-Temperature Pathways to Polycyclic Aromatic Hydrocarbons in the Interstellar Medium

    NASA Astrophysics Data System (ADS)

    Kaiser, Ralf I.; Parker, Dorian S. N.; Mebel, Alexander M.

    2015-04-01

    Bimolecular reactions of phenyl-type radicals with the C4 and C5 hydrocarbons vinylacetylene and (methyl-substituted) 1,3-butadiene have been found to synthesize polycyclic aromatic hydrocarbons (PAHs) with naphthalene and 1,4-dihydronaphthalene cores in exoergic and entrance barrierless reactions under single-collision conditions. The reaction mechanism involves the initial formation of a van der Waals complex and addition of a phenyl-type radical to the C1 position of a vinyl-type group through a submerged barrier. Investigations suggest that in the hydrocarbon reactant, the vinyl-type group must be in conjugation with a -C≡CH or -HC=CH2 group to form a resonantly stabilized free radical intermediate, which eventually isomerizes to a cyclic intermediate followed by hydrogen loss and aromatization (PAH formation). The vinylacetylene-mediated formation of PAHs might be expanded to more complex PAHs, such as anthracene and phenanthrene, in cold molecular clouds via barrierless reactions involving phenyl-type radicals, such as naphthyl, which cannot be accounted for by the classical hydrogen abstraction-acetylene addition mechanism.

  2. Polycyclic aromatic hydrocarbons produced by electrocautery smoke and the use of personal protective equipment 1

    PubMed Central

    Claudio, Caroline Vieira; Ribeiro, Renata Perfeito; Martins, Júlia Trevisan; Marziale, Maria Helena Palucci; Solci, Maria Cristina; Dalmas, José Carlos

    2017-01-01

    ABSTRACT Objective: analyze the concentration of polycyclic aromatic hydrocarbons in electrocautery smoke in operating rooms and the use of personal protective equipment by the intraoperative team when exposed to hydrocarbons. Method: exploratory and cross-sectional field research conducted in a surgery center. Gases were collected by a vacuum suction pump from a sample of 50 abdominal surgeries in which an electrocautery was used. A form was applied to identify the use of personal protective equipment. Gases were analyzed using chromatography. Descriptive statistics and Spearman's test were used to treat data. Results: there were 17 (34%) cholecystectomies with an average duration of 136 minutes, while the average time of electrocautery usage was 3.6 minutes. Airborne hydrocarbons were detected in operating rooms in 100% of the surgeries. Naphthalene was detected in 48 (96.0%) surgeries and phenanthrene in 49 (98.0%). The average concentration of these compounds was 0.0061 mg/m3 and a strong correlation (0.761) was found between them. The intraoperative teams did not use respirator masks such as the N95. Conclusion: electrocautery smoke produces gases that are harmful to the health of the intraoperative team, which is a concern considering the low adherence to the use of personal protective equipment. PMID:28301033

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

    PubMed

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

    2016-04-01

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

  4. Ion-polycyclic aromatic hydrocarbon collisions: kinetic energy releases for specific fragmentation channels

    NASA Astrophysics Data System (ADS)

    Reitsma, G.; Zettergren, H.; Boschman, L.; Bodewits, E.; Hoekstra, R.; Schlathölter, T.

    2013-12-01

    We report on 30 keV He2 + collisions with naphthalene (C10H8) molecules, which leads to very extensive fragmentation. To unravel such complex fragmentation patterns, we designed and constructed an experimental setup, which allows for the determination of the full momentum vector by measuring charged collision products in coincidence in a recoil ion momentum spectrometer type of detection scheme. The determination of fragment kinetic energies is found to be considerably more accurate than for the case of mere coincidence time-of-flight spectrometers. In fission reactions involving two cationic fragments, typically kinetic energy releases of 2-3 eV are observed. The results are interpreted by means of density functional theory calculations of the reverse barriers. It is concluded that naphthalene fragmentation by collisions with keV ions clearly is much more violent than the corresponding photofragmentation with energetic photons. The ion-induced naphthalene fragmentation provides a feedstock of various small hydrocarbonic species of different charge states and kinetic energy, which could influence several molecule formation processes in the cold interstellar medium and facilitates growth of small hydrocarbon species on pre-existing polycyclic aromatic hydrocarbons.

  5. Comparative electrochemical treatments of two chlorinated aliphatic hydrocarbons. Time course of the main reaction by-products.

    PubMed

    Randazzo, Serena; Scialdone, Onofrio; Brillas, Enric; Sirés, Ignasi

    2011-09-15

    Acidic aqueous solutions of the chlorinated aliphatic hydrocarbons 1,2-dichloroethane (DCA) and 1,1,2,2-tetrachloroethane (TCA) have been treated by the electro-Fenton (EF) process. Bulk electrolyses were performed at constant current using a BDD anode and an air diffusion cathode able to generate H(2)O(2) in situ, which reacts with added Fe(2+) to yield OH from Fenton's reaction. At 300 mA, almost total mineralization was achieved at 420 min for solutions containing 4mM of either DCA or TCA. Comparative treatments without Fe(2+) (anodic oxidation) or with a Pt anode led to a poorer mineralization. The better performance of the EF process with BDD is explained by the synergistic action of the oxidizing radicals, BDD(OH) at the anode surface and OH in the bulk, and the minimization of diffusional limitations. The decay of the initial pollutant accomplished with pseudo first-order kinetics. Chloroacetic and dichloroacetic acids were the major by-products during the degradation of DCA and TCA, respectively. Acetic, oxalic and formic acids were also identified. The proposed reaction pathways include oxidative and reductive (cathodic) dechlorination steps. Chlorine was released as Cl(-), being further oxidized to ClO(3)(-) and, mostly, to ClO(4)(-), due to the action of the largely generated BDD(OH) and OH.

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

    NASA Astrophysics Data System (ADS)

    Alberti, Luca; Lombi, Silvia; Zanini, Andrea

    2011-09-01

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

  7. Lipidic ionic liquid stationary phases for the separation of aliphatic hydrocarbons by comprehensive two-dimensional gas chromatography.

    PubMed

    Nan, He; Zhang, Cheng; O'Brien, Richard A; Benchea, Adela; Davis, James H; Anderson, Jared L

    2017-01-20

    Lipidic ionic liquids (ILs) possessing long alkyl chains as well as low melting points have the potential to provide unique selectivity as well as wide operating ranges when used as stationary phases in gas chromatography. In this study, a total of eleven lipidic ILs containing various structural features (i.e., double bonds, linear thioether chains, and cyclopropanyl groups) were examined as stationary phases in comprehensive two dimensional gas chromatography (GC×GC) for the separation of nonpolar analytes in kerosene. N-alkyl-N'-methyl-imidazolium-based ILs containing different alkyl side chains were used as model structures to investigate the effects of alkyl moieties with different structural features on the selectivities and operating temperature ranges of the IL-based stationary phases. Compared to a homologous series of ILs containing saturated side chains, lipidic ILs exhibit improved selectivity toward the aliphatic hydrocarbons in kerosene. The palmitoleyl IL provided the highest selectivity compared to all other lipidic ILs as well as the commercial SUPELCOWAX 10 column. The linoleyl IL containing two double bonds within the alkyl side chain showed the lowest chromatographic selectivity. The lipidic IL possessing a cyclopropanyl group within the alkyl moiety exhibited the highest thermal stability. The Abraham solvation parameter model was used to evaluate the solvation properties of the lipidic ILs. This study provides the first comprehensive examination into the relation between lipidic IL structure and the resulting solvation characteristics. Furthermore, these results establish a basis for applying lipidic ILs as stationary phases for solute specific separations in GC×GC.

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

    PubMed

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

    2013-11-01

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

  9. Sediment-associated aliphatic and aromatic hydrocarbons in coastal British Columbia, Canada: concentrations, composition, and associated risks to protected sea otters.

    PubMed

    Harris, Kate A; Yunker, Mark B; Dangerfield, Neil; Ross, Peter S

    2011-10-01

    Sediment-associated hydrocarbons can pose a risk to wildlife that rely on benthic marine food webs. We measured hydrocarbons in sediments from the habitat of protected sea otters in coastal British Columbia, Canada. Alkane concentrations were dominated by higher odd-chain n-alkanes at all sites, indicating terrestrial plant inputs. While remote sites were dominated by petrogenic polycyclic aromatic hydrocarbons (PAHs), small harbour sites within sea otter habitat and sites from an urban reference area reflected weathered petroleum and biomass and fossil fuel combustion. The partitioning of hydrocarbons between sediments and adjacent food webs provides an important exposure route for sea otters, as they consume ∼25% of their body weight per day in benthic invertebrates. Thus, exceedences of PAH sediment quality guidelines designed to protect aquatic biota at 20% of the sites in sea otter habitat suggest that sea otters are vulnerable to hydrocarbon contamination even in the absence of catastrophic oil spills.

  10. Determination of hydroxylated polycyclic aromatic hydrocarbons by HPLC-photoionization tandem mass spectrometry in wood smoke particles and soil samples.

    PubMed

    Avagyan, Rozanna; Nyström, Robin; Boman, Christoffer; Westerholm, Roger

    2015-06-01

    A simple and fast method for analysis of hydroxylated polycyclic aromatic hydrocarbons using pressurized liquid extraction and high performance liquid chromatography utilizing photoionization tandem mass spectrometry was developed. Simultaneous separation and determination of nine hydroxylated polycyclic aromatic hydrocarbons and two hydroxy biphenyls could be performed in negative mode with a run time of 12 min, including equilibration in 5 min. The calibration curves were in two concentration ranges; 1-50 ng/mL and 0.01-50 μg/mL, with coefficients of correlation R (2) > 0.997. The limits of detection and method quantification limits were in the range of 9-56 pg and 5-38 ng/g, respectively. A two-level full factorial experimental design was used for screening of conditions with the highest impact on the extraction. The extraction procedure was automated and suitable for a large number of samples. The extraction recoveries ranged from 70 to 102 % and the matrix effects were between 92 and 104 %. The overall method was demonstrated on wood smoke particles and soil samples with good analytical performance, and five OH-PAHs were determined in the concentration range of 0.19-210 μg/g. As far as we know, hydroxylated polycyclic aromatic hydrocarbons were determined in wood smoke and soil samples using photoionization mass spectrometry for the first time in this present study. Accordingly, this study shows that high performance liquid chromatography photoionization tandem mass spectrometry can be a good option for the determination of hydroxylated polycyclic aromatic hydrocarbons in complex environmental samples. Graphical Abstract The method developed in this study was used to determine hydroxylated polycyclic aromatic hydrocarbons in wood smoke and soil.

  11. Biosurfactant produced by novel Pseudomonas sp. WJ6 with biodegradation of n-alkanes and polycyclic aromatic hydrocarbons.

    PubMed

    Xia, Wenjie; Du, Zhifeng; Cui, Qingfeng; Dong, Hao; Wang, Fuyi; He, Panqing; Tang, YongChun

    2014-07-15

    Alkanes and polycyclic aromatic hydrocarbons (PAHs) have threatened the environment due to toxicity and poor bioavailability. Interest in degradation of these hazardous materials by biosurfactant-producing bacteria has been steadily increasing in recent years. In this work, a novel biosurfactant-producing Pseudomonas sp. WJ6 was isolated to degrade a wide range of n-alkanes and polycyclic aromatic hydrocarbons. Production of lipopeptide biosurfactant was observed in all biodegradable studies. These lipopeptides were purified and identified by C18 RP-HPLC system and electrospray ionization-mass spectrometry. Results of structural analysis showed that these lipopeptides generated from different hydrocarbons were classified to be surfactin, fengycin and lichenysin. Heavy-oil sludge washing experiments demonstrated that lipopeptides produced by Pseudomonas sp. WJ6 have 92.46% of heavy-oil washing efficiency. The obtained results indicate that this novel bacterial strain and its lipopeptides have great potentials in the environmental remediation and petroleum recovery.

  12. Health risk analysis of atmospheric polycyclic aromatic hydrocarbons in big cities of China.

    PubMed

    Wang, Yonghua; Hu, Liangfeng; Lu, Guanghua

    2014-05-01

    A probabilistic carcinogenic risk assessment of atmospheric polycyclic aromatic hydrocarbons (PAHs) in four big cities (Beijing, Shanghai, Guangzhou, Xiamen) of China was carried out. PAHs levels in these cities were collected from published literatures and converted into BaP equivalent (BaPeq) concentrations. The health risk assessment models recommended by US EPA were applied to quantitatively characterize the health risk values of PAHs. Monte Carlo simulation and sensitivity analysis were applied to quantify uncertainties of risk assessment. The results showed that BaPeq concentrations of four cities were all higher than the newest limited value (1 ng/m(3)) of China. Health risk assessment indicated that atmospheric PAHs in Guangzhou and Xiamen posed no or little carcinogenic risk on local residents. However, the PAHs in Beijing and Shanghai posed potential carcinogenic risk for adults and lifetime exposure. Notwithstanding the uncertainties, this study provides the primary information on the carcinogenic risk of atmospheric PAHs in studied cities of China.

  13. The phototoxicity of polycyclic aromatic hydrocarbons: a theoretical study of excited states and correlation to experiment.

    PubMed

    Betowski, Leon D; Enlow, Mark; Riddick, Lee

    2002-06-01

    Investigators using models to determine the phototoxic effects of sunlight on polycyclic aromatic hydrocarbons (PAHs) have invoked the excited states of the molecule as important in elucidating the mechanism of these reactions. Energies of actual excited states were calculated for ten PAHs by several ab initio methods. The main method used for these calculations was the Configuration Interaction approach, modeling excited states as combinations of single substitutions out of the Hartree-Fock ground state. These calculations correlate well with both experimentally measured singlet and triplet state energies and also previous HOMO-LUMO gap energies that approximate the singlet state energies. The excited state calculations then correlate well with general models of photo-induced toxicity based for the PAHs.

  14. Infrared frequencies and intensities for astrophysically important polycyclic aromatic hydrocarbon cations

    NASA Technical Reports Server (NTRS)

    Szczepanski, Jan; Vala, Martin

    1993-01-01

    Polycyclic aromatic hydrocarbons (PAHs) have been implicated as the carriers of the 'unidentified infrared' (UIR) emission bands observed from the interstellar medium. It has long been thought that these molecules, if present, probably exist as cations. In this paper we present infrared spectra of the cations of five moderate-sized PAHs. The PAH cations have been produced by low-energy electron impact and then trapped and stabilized in argon matrices at 12 K. To date, results have been obtained on naphthalene, anthracene, pyrene, perylene, and coronene. A common feature of the infrared spectra of all these cations is the very different intensity pattern of the ions compared to the neutral parents. Visible and (partial) infrared spectra of the coronene cation are also presented. It is shown that the out-of-plane CH bending mode shifts to a position very close to the UIR band at 11.3 microns. The astrophysical impact of these observations is discussed.

  15. Polycyclic aromatic hydrocarbon optical properties and contribution to the acceleration of stellar outflows

    NASA Technical Reports Server (NTRS)

    Cherchneff, Isabelle; Barker, John R.; Tielens, Alexander G. G. M.

    1991-01-01

    The optical constants of four polycyclic aromatic hydrocarbon (PAH) molecules (benzene, pyrene, pentacene, and coronene) are determined from their measured laboratory absorption spectra. The Planck mean of the radiation pressure cross section is computed for each molecule and for amorphous carbon (AC) grains, and semiempirically estimated for large PAH molecules up to 400 carbon atoms. Assuming that PAHs are present in carbon-rich stellar outflows, the radiation pressure forces acting on them are calculated and compared with the radiation forces on AC particles. The results show that PAHs possess very different optical properties from AC grains. Small PAHs may experience an 'inverse greenhouse' effect in the inner part of the envelope, as they decouple from the gas close to the photosphere. The radiation pressure force on PAHs is always much less than the force at work on AC grains, and PAH molecules do not affect significantly the dynamics of the outflow.

  16. [Carcinogenic risk of polycyclic aromatic hydrocarbons: classification and interpretation of the monitoring].

    PubMed

    Catalani, Simona; Fostinelli, Jacopo; Apostoli, Pietro

    2014-01-01

    The polycyclic aromatic hydrocarbons (PAHs) are widespread contaminants characterized by various chemical, physical and toxic properties. The characterization of occupational and environmental exposures and the use of suitable measurements protocols are very significant because their presence in mixtures and environmental persistency. In the past few years, the knowledge concerning carcinogenicity of PAHs have been reviewed, the mechanisms involved are the interaction of PAH's metabolites with DNA and oxidative damages. The main requirement for research concerns lack of knowledge on reference values and occupational exposure's assessment in particular PAHs sampling methods that can lead to combined measurements of vapor and aerosol mixtures. Aims of this study are to describe a possible occupational sources of PAHs providing also an update of mechanism involved in their carcinogenicity and risk calculation as is done in the TEF approach. The classifications provided by International Agencies and Institutions and the limit values adopted have been reviewed and taken into account.

  17. [Effect of microorganism for polycyclic aromatic hydrocarbons (PAHs) sorption on surface sediments and soils].

    PubMed

    Luo, Xue-Mei; He, Meng-Chang; Liu, Chang-Ming

    2007-02-01

    Influence of microorganism for polycyclic aromatic hydrocarbons (PAHs) sorption on surface sediments and soils in Yellow River Delta was studied. The results indicated that phenanthrene and benzo[a]pyrene could be adsorbed or biodegraded by Bacillus subtilis, and 98% phenanthrene and 85% benzo[a]pyrene was eliminated by microorganism in adsorption process. Sorption isotherms of soils and sediments with and without microorganism were described by linear isotherm equation. Adsorption capacity of samples with microorganism increased about 35 times than that of without microorganism, but benzo[a] pyrene adsorption capacity decreased about 2/3. In desorption process, samples with microorganism desorbed less phenanthrene than without microorganism, but more benzo[a]pyrene. Microorganism plays an important role in adsorption process.

  18. Sedimentary record of polycyclic aromatic hydrocarbons in a reservoir in Northeast China.

    PubMed

    Lin, Tian; Qin, Yanwen; Zheng, Binghui; Li, Yuanyuan; Zhang, Lei; Guo, Zhigang

    2012-04-01

    A sediment core from the Dahuofang Reservoir in Northeast China was (210)Pb and (137)Cs dated and analyzed for polycyclic aromatic hydrocarbons (PAHs) to track the regional PAH pollution in the past 50 years. The 2-4 ring PAHs peaked in the early 1990s, reflecting the historical role of coal usage in the energy structure in this area. More recently, vehicle emissions caused the continuous increase of the 5+6 ring PAHs. However, the sixteen US EPA priority PAHs showed a significant decline since the early 1990s. This PAH temporal trend is different from the U.S., the European countries and Japan, and is also different from the other areas of China, which could be attributed to the switch from coal to oil or natural gas as the main energy, and the large-scale elimination of outdated combustion facilities and techniques in Northeast China.

  19. Molecular Growth Inside of Polycyclic Aromatic Hydrocarbon Clusters Induced by Ion Collisions.

    PubMed

    Delaunay, Rudy; Gatchell, Michael; Rousseau, Patrick; Domaracka, Alicja; Maclot, Sylvain; Wang, Yang; Stockett, Mark H; Chen, Tao; Adoui, Lamri; Alcamí, Manuel; Martín, Fernando; Zettergren, Henning; Cederquist, Henrik; Huber, Bernd A

    2015-05-07

    The present work combines experimental and theoretical studies of the collision between keV ion projectiles and clusters of pyrene, one of the simplest polycyclic aromatic hydrocarbons (PAHs). Intracluster growth processes induced by ion collisions lead to the formation of a wide range of new molecules with masses larger than that of the pyrene molecule. The efficiency of these processes is found to strongly depend on the mass and velocity of the incoming projectile. Classical molecular dynamics simulations of the entire collision process-from the ion impact (nuclear scattering) to the formation of new molecular species-reproduce the essential features of the measured molecular growth process and also yield estimates of the related absolute cross sections. More elaborate density functional tight binding calculations yield the same growth products as the classical simulations. The present results could be relevant to understand the physical chemistry of the PAH-rich upper atmosphere of Saturn's moon Titan.

  20. Air pollution from a large steel factory: polycyclic aromatic hydrocarbon emissions from coke-oven batteries

    SciTech Connect

    Lorenzo Liberti; Michele Notarnicola; Roberto Primerano; Paolo Zannetti

    2006-03-15

    A systematic investigation of solid and gaseous atmospheric emissions from some coke-oven batteries of one of Europe's largest integrated steel factory (Taranto, Italy) has been carried out. These emissions, predominantly diffuse, originate from oven leakages, as well as from cyclic operations of coal loading and coke unloading. In air monitoring samples, polycyclic aromatic hydrocarbons (PAHs) were consistently detected at concentrations largely exceeding threshold limit values. By means of PAHs speciation profile and benzo-(a)pyrene (BaP) equivalent dispersion modeling from diffuse sources, the study indicated that serious health risks exist not only in working areas, but also in a densely populated residential district near the factory. 30 refs., 5 figs., 3 tabs.

  1. Atypical kinetic behavior of chloroperoxidase-mediated oxidative halogenation of polycyclic aromatic hydrocarbons.

    PubMed

    Aburto, Jorge; Correa-Basurto, Jose; Torres, Eduardo

    2008-12-01

    We have identified an atypical kinetic behavior for the oxidative halogenation of several polycyclic aromatic hydrocarbons (PAHs) by chloroperoxidase (CPO) from Caldariomyces fumago. This behavior resembles the capacity of some members of the P450 family to simultaneously recognize several substrate molecules at their active sites. Indeed, fluorometric studies showed that PAHs exist in solution as monomers and pi-pi dimers that interact to different extents with CPO. The dissociation constants of dimerization were evaluated for every single PAH by spectrofluorometry. Furthermore, docking studies also suggest that CPO might recognize either one or two substrate molecules in its active site. The atypical sigmoidal kinetic behavior of CPO in the oxidative halogenation of PAHs is explained in terms of different kinetic models for non-heteroatomic PAHs (naphthalene, anthracene and pyrene). The results suggest that the actual substrate for CPO in this study was the pi-pi dimer for all evaluated PAHs.

  2. Role of volcanic dust in the atmospheric transport and deposition of polycyclic aromatic hydrocarbons and mercury.

    PubMed

    Stracquadanio, Milena; Dinelli, Enrico; Trombini, Claudio

    2003-12-01

    The role of volcanic ash as scavenger of atmospheric pollutants, in their transport and final deposition to the ground is examined. Attention is focused on polycyclic aromatic hydrocarbons (PAHs) and on particulate mercury (Hgp). The ash-fall deposits studied belong to the 2001 and 2002 eruptive activity of Mount Etna, Southern Italy, and were investigated at three (2001) and four (2002) sites downwind of the major tephra dispersal pattern. The dry deposition of mercury and PAHs was determined, and, in particular, a downward flux to the ground of PAHs (approximately 7.29 microg m(-2) per day) and mercury (750 ng m(-2) per day) was estimated in Catania from October 26 to October 28, 2002. Finally, evidence on the anthropogenic origin of PAHs scavenged from the troposphere by volcanic ash is supported by the analysis of PAH compositions in granulometrically homogeneous fractions.

  3. Arbuscular mycorrhizal fungal hyphae contribute to the uptake of polycyclic aromatic hydrocarbons by plant roots.

    PubMed

    Gao, Yanzheng; Cheng, Zhaoxia; Ling, Wanting; Huang, Jing

    2010-09-01

    The arbuscular mycorrhizal (AM) hyphae-mediated uptake of polycyclic aromatic hydrocarbons (PAHs) by the roots of ryegrass (Lolium multiflorum Lam.) was investigated using three-compartment systems. Glomus mosseae and Glomus etunicatum were chosen, and fluorene and phenanthrene were used as representative PAHs. When roots were grown in un-spiked soils, AM hyphae extended into PAH-spiked soil and clearly absorbed and transported PAHs to roots, resulting in high concentrations of fluorene and phenanthrene in roots. This was further confirmed by the batch equilibration experiment, which revealed that the partition coefficients (K(d)) of tested PAHs by mycorrhizal hyphae were 270-356% greater than those by roots, suggesting the great potential of hyphae to absorb PAHs. Because of fluorene's lower molecular weight and higher water solubility, its translocation by hyphae was greater than that of phenanthrene. These results provide new perspectives on the AM hyphae-mediated uptake by plants of organic contaminants from soil.

  4. Occurrence of polycyclic aromatic hydrocarbons in dust emitted from circulating fluidized bed boilers.

    PubMed

    Kozielska, B; Konieczyńiski, J

    2008-11-01

    Occurrence of polycyclic aromatic hydrocarbons (PAHs) in granulometric fractions of dust emitted from a hard coal fired circulating fluidized bed (CFB) boiler was investigated. The dust was sampled with the use of a Mark III impactor. In each fraction of dust, by using gas chromatography (GC), 16 selected PAHs and total PAHs were determined and the toxic equivalent B(a)P (TE B(a)P) was computed. The results, recalculated for the standard granulometric fractions, are presented as concentrations and content of the determined PAHs in dust. Distributions of PAHs and their profiles in the granulometric dust fractions were studied also. The PAHs in dust emitted from the CFB boiler were compared with those emitted from mechanical grate boilers; a distinctly lower content of PAHs was found in dust emitted from the former.

  5. Polycyclic aromatic hydrocarbons loads into the Mediterranean Sea: estimate of Sarno River inputs.

    PubMed

    Montuori, Paolo; Triassi, Maria

    2012-03-01

    The polycyclic aromatic hydrocarbons (PAHs) pollution in the Sarno River and its environmental impact on the Gulf of Naples (Tyrrhenian Sea, Central Mediterranean Sea) were estimated. The 16 PAHs identified by the USEPA as priority pollutants and perylene were determined in the water dissolved phase (DP), suspended particulate matter (SPM) and sediments. Total PAHs concentrations ranged from 23.1 to 2670.4 ng L(-1) in water (sum of DP and SPM) and from 5.3 to 678.6 ng g(-1) in sediment samples. Source analysis revealed that PAHs mainly came from combustion process. Contaminant discharges of PAHs into the sea were calculated in about 8530 gd(-1) showing that this river should account as one of the main contribution sources of PAHs to the Tyrrhenian Sea.

  6. Effect of concentration on sequestration and bioavailability of two polycyclic aromatic hydrocarbons

    SciTech Connect

    Chung, N.; Alexander, M.

    1999-10-15

    A study was conducted to determine the effect of concentration on sequestration and bioavailability of phenanthrene and pyrene in soil. The compounds at 1.0, 10, and 100 mg/kg of soil became increasingly resistant to a mild solvent extraction and progressively less bioavailable to earthworms (Eisenia foetida) as a result of aging for 120 days. Aging also resulted in both compounds at 1.0 and 10 mg/kg and phenanthrene but not pyrene at 100 mg/kg becoming more resistant to microbial degradation. Increasing the concentration led to an increase in the percentages of the unaged and aged compounds that were susceptible to microbial degradation. Some of each of the two compounds was still available to earthworms following biodegradation. The data show that sequestration of the polycyclic aromatic hydrocarbons occurs at both low and high concentrations.

  7. Inversion and rotation processes involving non-planar aromatic compounds catalyzed by extended polycyclic aromatic hydrocarbons

    NASA Astrophysics Data System (ADS)

    Karton, Amir

    2014-10-01

    Using accurate quantum chemical calculations, we show that extended planar polycyclic aromatic hydrocarbons (PAHs) can efficiently catalyze a range of chemical processes involving non-planar aromatic systems. These include (i) bowl-to-bowl inversion of curved PAHs (e.g. corannulene and sumanene), (ii) 'flip-flop' inversion of helicenes (e.g. benzo[c]phenanthrene), and (iii) rotation about the Phsbnd Ph bond in biphenyls. Non-covalent π-π interactions between the planar catalyst and the substrate stabilize the planar transition structures to a greater extent than they stabilize the non-planar reactants. These result in surprisingly large catalytic enhancements (namely, the reaction barrier heights are reduced by 21-63% of the uncatalyzed reaction barriers).

  8. Approaches for externally validated QSAR modelling of Nitrated Polycyclic Aromatic Hydrocarbon mutagenicity.

    PubMed

    Gramatica, P; Pilutti, P; Papa, E

    2007-01-01

    Nitrated Polycyclic Aromatic Hydrocarbons (nitro-PAHs), ubiquitous environmental pollutants, are recognized mutagens and carcinogens. A set of mutagenicity data (TA100) for 48 nitro-PAHs was modeled by the Quantitative Structure-Activity Relationships (QSAR) regression method, and OECD principles for QSAR model validation were applied. The proposed Multiple Linear Regression (MLR) models are based on two topological molecular descriptors. The models were validated for predictivity by both internal and external validation. For the external validation, three different splitting approaches, D-optimal Experimental Design, Self Organizing Maps (SOM) and Random Selection by activity sampling, were applied to the original data set in order to compare these methodologies and to select the best descriptors able to model each prediction set chemicals independently of the splitting method applied. The applicability domain was verified by the leverage approach.

  9. Isomer discrimination of polycyclic aromatic hydrocarbons in the Murchison meteorite by resonant ionization.

    PubMed

    Callahan, Michael P; Abo-Riziq, Ali; Crews, Bridgit; Grace, Louis; de Vries, Mattanjah S

    2008-12-15

    We have used two-color resonant two-photon ionization (2C-R2PI) mass spectrometry to discriminate between isomers of polycyclic aromatic hydrocarbons in the Murchison meteorite. We measured the 2C-R2PI spectra of chrysene and triphenylene seeded in a supersonic jet by laser desorption. Since each isomer differs in its R2PI spectrum, we can distinguish between isomers using wavelength dependent ionization and mass spectrometry. We found both chrysene and triphenylene in sublimates from carbonaceous residue obtained by acid demineralization of the Murchison meteorite. Their R2PI mass spectra show only the molecular ion, even though these samples contain a complex inventory of organic molecules.

  10. Evaluation of cytochrome P450{sub BS{beta}} reactivity against polycyclic aromatic hydrocarbons and drugs

    SciTech Connect

    Torres, Eduardo; Hayen, Heiko; Niemeyer, Christof M.; E-mail: christof.niemeyer@uni-dortmund.de

    2007-03-30

    The oxidation of 10 polycyclic aromatic hydrocarbons (PAH) by cytochrome P450{sub BS{beta}} using three different electron acceptors is reported. Three PAH were found to be substrates for the oxidation by P450{sub BS{beta}}, namely anthracene, 9-methyl-anthracene and azulene. The respective oxidation products were identified by reversed-phase high-performance liquid chromatography coupled to electrospray ionization-mass spectrometry. In addition, 10 drug-like compounds were investigated for their effects on the catalytic activity of P450{sub BS{beta}} by carrying out inhibition studies. The stability of P450{sub BS{beta}} against hydrogen peroxide, cumene, and ter-butyl hydroperoxide was determined. Overall, the results of this study suggested that the P450{sub BS{beta}} enzyme represents a powerful catalyst in terms of the catalytic activity and operational stability.

  11. Modeling the unidentified infrared emission with combinations of polycyclic aromatic hydrocarbons.

    PubMed

    Allamandola, L J; Hudgins, D M; Sandford, S A

    1999-02-01

    The infrared emission band spectrum associated with many different interstellar objects can be modeled successfully by using combined laboratory spectra of neutral and positively charged polycyclic aromatic hydrocarbons (PAHs). These model spectra, shown here for the first time, alleviate the principal spectroscopic criticisms previously leveled at the PAH hypothesis and demonstrate that mixtures of free molecular PAHs can indeed account for the overall appearance of the widespread interstellar infrared emission spectrum. Furthermore, these models give us insight into the structures, stabilities, abundances, and ionization balance of the interstellar PAH population. These, in turn, reflect conditions in the emission zones and shed light on the microscopic processes involved in the carbon nucleation, growth, and evolution in circumstellar shells and the interstellar medium.

  12. Polycyclic aromatic hydrocarbon-DNA adducts in Beluga whales from the Arctic

    SciTech Connect

    Mathieu, A.; Payne, J.F.; Fancey, L.L.

    1997-09-01

    The Arctic is still relatively pristine in nature, but it is also vulnerable to pollution because contaminants originating from midlatitudes are transported to the Arctic by atmospheric processes, ocean currents, and river. Recognition of this fact of Arctic vulnerability has resulted in a Declaration on the Protection of the Arctic Environment by eight Arctic countries. A manifest aim of this declaration is to develop an Arctic Monitoring and Assessment Program. We report here on the presence of measurable levels of polycyclic aromatic hydrocarbon-DNA adducts, including relatively high levels in Arctic beluga (Delphinapterus leucas). These results lend support to the value of developing biological assessment programs for Arctic wildlife. 15 refs., 1 tab.

  13. Residues of organochlorine pesticides and polycyclic aromatic hydrocarbons in drinking water of Ahmedabad City, India

    SciTech Connect

    Jani, J.P.; Mistry, J.S. ); Raiyani, C.V.; Patel, J.S.; Desai, N.M.; Kashyap, S.K. )

    1991-09-01

    The ubiquitous environmental pollutants organochlorine pesticides (OCP) and polycyclic aromatic hydrocarbons (PAH) have been extensively studied for their toxicity. Monitoring of OCP and PAH residues has always been considered important for controlling human exposure. As compared to several other countries, the higher body burden of OCP in Indian general population is indicative of higher exposure to these chemicals. Recent studies have shown higher residues of OCP in food commodities including human mother's milk. The levels of OCP in drinking water is still a matter of concern and practically nothing is known about the residues of PAH in drinking water in India. This is the first report of its kind regarding the residues of OCP and PAH in drinking water of Ahmedabad City, the sixth largest city of India with a population of more than 2.5 million.

  14. Mycobacterium pyrenivorans sp. nov., a novel polycyclic-aromatic-hydrocarbon-degrading species.

    PubMed

    Derz, Kerstin; Klinner, Ulrich; Schuphan, Ingolf; Stackebrandt, Erko; Kroppenstedt, Reiner M

    2004-11-01

    The taxonomic position of a polycyclic-aromatic-hydrocarbon-degrading bacterium, strain 17A3(T), isolated from contaminated soil was determined using a combination of phenotypic and genotypic properties. The isolate showed phenotypic properties that were diagnostic for species of the genus Mycobacterium. Comparative 16S rRNA gene sequence analysis assigned 17A3(T) to the 16S rRNA gene subgroup that contains Mycobacterium aurum, Mycobacterium austroafricanum, Mycobacterium vaccae and Mycobacterium vanbaalenii, but it could clearly be distinguished from these species using a combination of physiological, chemotaxonomic markers and internal rRNA gene spacer analyses. The data showed that strain 17A3(T) (=DSM 44605(T)=NRRL B-24244(T)) merits recognition as the type strain of a novel species of the genus Mycobacterium. The name Mycobacterium pyrenivorans sp. nov. is proposed for the species because of its ability to use pyrene as a sole source of carbon and energy.

  15. Polycyclic aromatic hydrocarbons in coastal sediment of klang strait, Malaysia: distribution pattern, risk assessment and sources.

    PubMed

    Tavakoly Sany, Seyedeh Belin; Hashim, Rosli; Salleh, Aishah; Rezayi, Majid; Mehdinia, Ali; Safari, Omid

    2014-01-01

    Concentration, source, and ecological risk of polycyclic aromatic hydrocarbons (PAHs) were investigated in 22 stations from surface sediments in the areas of anthropogenic pollution in the Klang Strait (Malaysia). The total PAH level in the Klang Strait sediment was 994.02±918.1 µg/kg dw. The highest concentration was observed in stations near the coastline and mouth of the Klang River. These locations were dominated by high molecular weight PAHs. The results showed both pyrogenic and petrogenic sources are main sources of PAHs. Further analyses indicated that PAHs primarily originated from pyrogenic sources (coal combustion and vehicular emissions), with significant contribution from petroleum inputs. Regarding ecological risk estimation, only station 13 was moderately polluted, the rest of the stations suffered rare or slight adverse biological effects with PAH exposure in surface sediment, suggesting that PAHs are not considered as contaminants of concern in the Klang Strait.

  16. Determination of thiaarenes and polycyclic aromatic hydrocarbons in workplace air of an aluminum reduction plant

    SciTech Connect

    Becker, G.; Colmsjoe, A.; Oestman, C.

    1999-05-01

    Quantitation of a variety of tetra-, penta-, and hexacyclic aromatic sulfur heterocycles (thiaarenes) in workplace air of an aluminum reduction plant has been made by help of gas chromatography with atomic emission detection (GC-AED). Personal exposure to those thiaarenes and to polycyclic aromatic hydrocarbons depending on work categories has been evaluated. Summarized concentrations of the thiaarenes investigated have been found to be 0.4--19.0 {micro}g/m{sup 3}. When using sulfur selective AED, samples could be analyzed without a prior separation of the thiaarenes from the PAH. The present data indicate a contribution of thiaarenes to the overall toxicity of coal tar pitch volatiles in this work environment.

  17. Persistent organic pollutants and polycyclic aromatic hydrocarbons in mosses after fire at the Brazilian Antarctic Station.

    PubMed

    Colabuono, Fernanda Imperatrice; Taniguchi, Satie; Cipro, Caio Vinícius Zecchin; da Silva, Josilene; Bícego, Márcia Caruso; Montone, Rosalinda Carmela

    2015-04-15

    A fire at the Brazilian Antarctic Station on February 25th, 2012 led to the burning of material that produced organic pollutants. To evaluate the impact in the surrounding area, polycyclic aromatic hydrocarbons (PAHs) and persistent organic pollutants (POPs) were analyzed in moss samples collected in the vicinities of the station before and after the incident and compared to findings from previous studies in the same region. PCBs were on the same magnitude as that reported in previous studies, which could be associated to the global dispersion of these compounds and may not be related to the local fire. In contrast, concentrations of HCB and PAHs were higher than those reported in previous studies. No PBDEs were found above the method detection limit. Organic contaminant concentrations in mosses decreased a few months after the fire, which is an important characteristic when considering the use of mosses for monitoring recent exposure.

  18. Proposal of a procedure for the analysis of atmospheric polycyclic aromatic hydrocarbons in mosses.

    PubMed

    Concha-Graña, Estefanía; Piñeiro-Iglesias, María; Muniategui-Lorenzo, Soledad; López-Mahía, Purificación; Prada-Rodríguez, Darío

    2015-03-01

    A useful analytical procedure for the analysis of 19 polycyclic aromatic hydrocarbons (PAHs) in moss samples using microwave assisted extraction and programmed temperature vaporization-gas chromatography-tandem mass spectrometry (PTV-GC-MS/MS) determination is proposed. The state of art in PAHs analysis in mosses was reviewed. All the steps of the analysis were optimized regarding not only to the analytical parameters, but also the cost, the total time of analysis and the labour. The method was validated for one moss species used as moss monitor in ambient air, obtaining high recoveries (between 83-108%), low quantitation limits (lower than 2 ng g(-1)), good intermediate precision (relative standard deviation lower than 10%), uncertainties lower than 20%. Finally, the method was checked for other species, demonstrating its suitability for the analysis of different moss species. For this reason the proposed method can be helpful in air biomonitoring studies.

  19. Polycyclic aromatic hydrocarbons in pyrogenic soils of swampy landscapes of the Meshchera lowland

    NASA Astrophysics Data System (ADS)

    Tsibart, A. S.; Gennadiev, A. N.; Koshovskii, T. S.; Gamova, N. S.

    2016-03-01

    The composition and distribution of polycyclic aromatic hydrocarbons (PAHs) were studied in organomineral and organic soils of the Meshchera National Park. It was found that the background oligotrophic peat soils unaffected by fires in central parts of the bogs are characterized by the increased PAH concentrations due to their high sorption capacity. The fires of 2007 and 2010 resulted in the transformation of the plant cover and soil morphology, the formation of new horizons, and the change in the PAHs content and composition. Significant burn-off of organic matter was found in oligotrophic-eutrophic soils and resulted in the decrease of PAHs content after fire. Only partial burn-off of organic horizons and intense formation of PAHs were recorded in the soil with initially great thickness of peat horizons. Pyrogenic accumulation of PAHs was identified in organomineral soils of the marginal parts of bogs and of forest sites.

  20. Polycyclic aromatic hydrocarbons (PAHs) in bio-crudes from induction-heating pyrolysis of biomass wastes.

    PubMed

    Tsai, Wen-Tien; Mi, Hsiao-Hsuan; Chang, Yuan-Ming; Yang, Shyh-Yu; Chang, Jeng-Hung

    2007-03-01

    The aim of this work was to prepare the bio-crudes from agricultural wastes (i.e., rice straw, rice husk, sugarcane bagasse and coconut shell) by using induction-heating pyrolysis at specified conditions. The quantitative analysis of 21 priority pollutant polycyclic aromatic hydrocarbons (PAHs) in bio-crudes examined using gas chromatography/mass spectrometry (GC/MS) revealed that the PAHs in bio-crudes were primarily dominant in the low molecular weight (LMW) PAHs, including naphthalene (1.10-2.45 mg/L) and acenaphthene (0.72-7.61 mg/L). However, by considering carcinogenic potency, the bio-crudes from rice husk and sugarcane bagasse contained higher contents of benzo[a]pyrene (BaP) (0.52 and 0.92 mg/L, respectively) as compared to those from rice straw and coconut shell.

  1. Comparison of polycyclic aromatic hydrocarbon pollution in Chinese and Japanese residential air.

    PubMed

    Lu, Hao; Amagai, Takashi; Ohura, Takeshi

    2011-01-01

    Comparative studies on polycyclic aromatic hydrocarbon (PAH) pollution in residential air of Hangzhou (China) and Shizuoka (Japan) were conducted in summer (August, 2006) and winter (January, 2007). Total concentrations of 8 PAHs ranged from 7.1 to 320 ng/m3 and 0.15 to 35 ng/m3 in residential air of Hangzhou and Shizuoka, respectively. Air PAH concentrations in smoking houses were higher than that in nonsmoking houses. In nonsmoking houses, mothball emission and cooking practice were the emission sources of 2- and 3-ring PAHs in Hangzhou, respectively. The 2- and 3-ring PAHs were from use of insect repellent, kerosene heating and outdoor environment in nonsmoking houses in Shizuoka. The 5- and 6-ring PAHs in residential air were mainly from outdoor environment in both cities. Toxicity potencies of PAHs in residential air of Hangzhou were much higher than that in Shizuoka.

  2. Distributions and health risks of polycyclic aromatic hydrocarbons (PAHs) in atmospheric aerosols of Kuala Lumpur, Malaysia.

    PubMed

    Omar, Nasr Yousef M J; Mon, Tan Chin; Rahman, Noorsaadah A; Abas, M Radzi Bin

    2006-10-01

    The concentrations and distributions of particle bound polycyclic aromatic hydrocarbons (PAHs) collected over a 10 month period in ambient environment, at street levels as well as during a hazy episode are reported. Ambient and street level distributions of PAHs were similar and their occurrence was attributed to vehicular emissions. However, in haze particles, a different pattern of PAHs was observed, characterized by relatively low levels of benzo[a]pyrene (BaP) and high levels of benzofluoranthenes (BFs). The BaP equivalency results showed that the potential health risk associated with haze smoke particles was 4 times higher than that of street level particles whereas the lowest health risk was associated with ambient atmospheric particles.

  3. Characterization of polycyclic aromatic hydrocarbon emission from open burning of joss paper

    NASA Astrophysics Data System (ADS)

    Rau, Jui-Yeh; Tseng, Hui-Hsin; Lin, Min-Der; Wey, Ming-Yen; Lin, Yu-Hao; Chu, Chien-Wei; Lee, Ching-Hwa

    The concentration of polycyclic aromatic hydrocarbons (PAHs) in the ambient air from a massive open burning of joss paper was simultaneously measured at an open-burning site (OS) and a downwind site (DS) from 6 to 8 August 2006. A total of 16 major PAHs (particle-bound and gas-phase) concentrations were extracted by the Soxhlet analytical method and analyzed by gas chromatography. The dominant PAHs of the total mass of the organic compound at both the sampling sites were low-molecular-weight species. Further, the results showed that the start burning/end burning-dominant PAH concentration ratios at the OS and DS were 10 and 6.2, respectively. Diagnostic ratios were also used in this study to characterize and identify the PAH emission sources. The results suggest that the characterization of air pollutants emitted from open-burning joss paper lies between furnace-burning joss paper and wood combustion.

  4. Identification and Spectral Properties of Polycyclic Aromatic Hydrocarbons in Carbonaceous Soot Produced by Laser Pyrolysis

    NASA Astrophysics Data System (ADS)

    Jäger, C.; Krasnokutski, S.; Staicu, A.; Huisken, F.; Mutschke, H.; Henning, Th.; Poppitz, W.; Voicu, I.

    2006-10-01

    Carbon soot has been prepared by laser-induced pyrolysis of a mixture of ethylene (C2H4) and benzene (C6H6) vapor. The soluble part of the carbonaceous powder has been separated from its insoluble counterpart by soxhlet extraction in toluene. Several techniques were applied to obtain information on the composition of the extract. These included UV/visible and IR spectroscopy in solid and liquid phase, gas chromatography combined with mass spectrometry, gas-phase laser spectroscopy in a supersonic jet, and matrix spectroscopy in helium droplets, the latter being also combined with mass spectrometry. The analysis revealed that the carbonaceous powder contained various polycyclic aromatic hydrocarbons (PAHs). The highest concentration was found for the three-membered catacondensed PAHs, phenanthrene and anthracene. The results are discussed in view of the possible role of these molecules as interstellar dust components.

  5. Pressurized liquid extraction of polycyclic aromatic hydrocarbons from silicone rubber passive samplers.

    PubMed

    Shahpoury, Pourya; Hageman, Kimberly J

    2013-11-01

    Silicone rubber passive samplers effectively concentrate organic contaminants from water and are simple-to-use and robust. However, during the extraction of analytes from the samplers with organic solvents, oligomers associated with the rubber are inevitably extracted and this creates analytic challenges. Additionally, extraction methods that use Soxhlet or shaking are time-consuming and use large volumes of solvent. We evaluated a new method for the extraction of polycyclic aromatic hydrocarbons from silicone rubber passive samplers that uses pressurized liquid extraction with gel permeation chromatography. Extraction with dichloromethane at 100°C provided better recoveries compared to that of 50°C. The recoveries of 14 individual PAHs ranged from 81% to 102% and the mean recovery was 93% (standard deviation=7). Relative to comparable methods in which Soxhlet or shaking were used for the extraction, this method uses considerably less solvent and time.

  6. Simplified measurement technique for polycyclic aromatic hydrocarbons using the EPA Method 5 sampling train

    SciTech Connect

    Jacko, R.B.; Holcomb, M.L.

    1984-02-01

    Polycyclic aromatic hydrocarbons (PAH) are emitted from a variety of processes, including combustion processes, that are often scrutinized for other air pollutants including particulate matter and inorganic oxides. Studies have shown that some PAH compounds are carcinogenic, thus stimulating interest in quantifying and studying the influence of various system parameters on PAH emissions. A problem is encountered when PAH measurements are required is selection of a sampling train suitable for quantifying both particulate and PAH compounds. Previous studies, where PAH compounds have been measured, have employed EPA Method 5 with various modifications to make it more suitable for collection of volatile and reactive organic compounds. The paper describes a technique using an adsorbent packed column that is easily retrofitted to the Method 5 sampling train and used with a standard soxhlet extraction apparatus. The adsorbent is contained in a stainless steel canister that is inserted in a Method 5 bubbler and later in an extraction soxhlet, thus eliminating the need for transferring adsorbent.

  7. A Stable Saddle-Shaped Polycyclic Hydrocarbon with an Open-Shell Singlet Ground State.

    PubMed

    Ma, Ji; Liu, Junzhi; Baumgarten, Martin; Fu, Yubin; Tan, Yuan-Zhi; Schellhammer, Karl Sebastian; Ortmann, Frank; Cuniberti, Gianaurelio; Komber, Hartmut; Berger, Reinhard; Müllen, Klaus; Feng, Xinliang

    2017-03-13

    Diindeno-fused bischrysene, a new diindeno-based polycyclic hydrocarbon (PH), was synthesized and characterized. It was elucidated in detailed experimental and theoretical studies that this cyclopenta-fused PH possesses an open-shell singlet biradical structure in the ground state and exhibits high stability under ambient conditions (t1/2 =39 days). The crystal structure unambiguously shows a novel saddle-shaped π-conjugated carbon skeleton due to the steric hindrance of the central cove-edged bischrysene unit. UV/Vis spectral measurements revealed that the title molecule has a very narrow optical energy gap of 0.92 eV, which is consistent with the electrochemical analysis and further supported by density functional theory (DFT) calculations.

  8. Contamination and ecotoxicology risks of polycyclic aromatic hydrocarbons in Shantou coastal waters, China.

    PubMed

    Maskaoui, Khalid; Hu, Zhong

    2009-02-01

    Nine locations in Shantou coastal waters were chosen for the study on contamination and ecotoxicology risks posed by polycyclic aromatic hydrocarbons (PAHs). Sediment samples were collected to investigate PAH distribution behaviour, sources and understand their origin, which is fundamental in predicting their subsequent behaviour. Many approaches and methods were applied to accomplish these objectives and study purpose. The results found revealed the critical importance of improving our understanding of PAH equilibrium relationships. The serious environmental and health concern, imposed by the high concentrations of PAHs in the area, were widely discussed. Furthermore, the location of Shantou within the town and vicinity of Guiyu, which is a booming E-waste processing centre in China, might explain the significance of atmospheric transportation source of PAHs and enhance the occurrence of air-water exchange.

  9. THE INFRARED SPECTRA OF POLYCYCLIC AROMATIC HYDROCARBONS WITH SOME OR ALL HYDROGEN ATOMS REMOVED

    SciTech Connect

    Bauschlicher, Charles W. Jr.; Ricca, Alessandra E-mail: Alessandra.Ricca-1@nasa.gov

    2013-10-20

    The loss of one hydrogen from C{sub 96}H{sub 24} does not significantly affect the infrared spectra of the neutral, cation, or anion. Excluding a very weak C-C stretching band at 5.1 μm, the loss of two adjacent duo hydrogens does not significantly affect the spectra compared with the parent. Removing all of the hydrogen atoms significantly increases the intensity of the new C-C stretching band, and, for the cation, shifts it to a longer (5.2 μm) wavelength. Observations show a feature near 5.25 μm, which has been attributed to overtone and combination bands from polycyclic aromatic hydrocarbons (PAHs). This current work suggests that dehydrogenated PAHs might also contribute to this band, but its weakness implies that fully dehydrogenated cationic or dicationic species are very rare.

  10. City air pollution of polycyclic aromatic hydrocarbons and other mutagens: occurrence, sources and health effects.

    PubMed

    Nielsen, T; Jørgensen, H E; Larsen, J C; Poulsen, M

    1996-10-28

    The presence of polycyclic aromatic hydrocarbons (PAH), mutagens and other air pollutants was investigated in a busy street in central Copenhagen and in a park area adjacent to the street. The winter concentration of benzo(a)pyrene was 4.4 +/- 1.2 ng/m3 in the street air and 1.4 +/- 0.6 ng/m3 in the city park. The atmospheric concentrations of PAH decreased in the order of: street > city background air approximately suburbs > village > open land. The traffic contribution of PAH to street air was estimated to be 90% on working days and 60% during weekends and its contribution to city background air was estimated to be 40%. Four different approaches to evaluate the health effects are discussed. The direct effect of PAH air pollution, and other mutagens, is considered to be a maximum of five lung cancer cases each year out of one million people.

  11. Estimation and characterization of polycyclic aromatic hydrocarbons from magnesium metallurgy facilities in China.

    PubMed

    Nie, Zhiqiang; Yang, Yufei; Tang, Zhenwu; Liu, Feng; Wang, Qi; Huang, Qifei

    2014-11-01

    Field monitoring was conducted to develop a polycyclic aromatic hydrocarbon (PAH) emission inventory for the magnesium (Mg) metallurgy industry in China. PAH emissions in stack gas and fly/bottom ash samples from different smelting units of a typical Mg smelter were measured and compared. Large variations of concentrations, congener patterns, and emission factors of PAHs during the oxidation and reduction stages in the Mg smelter were observed. The measured average emission factor (166,487 μg/t Mg) was significantly higher than those of other industrial sources. Annual emission from Mg metallurgy in 2012 in China was estimated at 116 kg (514 g BaPeq) for PAHs. The results of this study suggest that PAH emission from Mg industries should be considered by local government agencies. These data may be helpful for understanding PAH levels produced by the Mg industry and in developing a PAH inventory.

  12. Action of a fluoranthene-utilizing bacterial community on polycyclic aromatic hydrocarbon components of creosote

    SciTech Connect

    Mueller, J.G.; Chapman, P.J.; Pritchard, P.H.

    1989-01-01

    Cultures enriched by serial transfer through a mineral salts medium containing fluoranthene were used to establish a stable, 7-membered bacterial community from a sandy soil highly contaminated with coal-tar creosote. This community exhibited an ability to utilize fluoranthene as sole carbon source for growth as demonstrated by increases in protein concentration and changes in absorption spectra when grown on fluoranthene in liquid culture. Biotransformation of other polycyclic aromatic hydrocarbons (PAHs) were verified by demonstrating their disappearance from an artificial PAH mixture using capillary gas chromatography. When grown on fluoranthene as sole carbon source and subsequently exposed to fluoranthene plus 16 additional PAHs typical of those found in creosote, this community transformed all PAHs present in this defined mixture. Continued incubation resulted in extensive degradation of the remaining 4 compounds.

  13. Use of antioxidant enzymes of clam Ruditapes philippinarum as biomarker to polycyclic aromatic hydrocarbon pollution

    NASA Astrophysics Data System (ADS)

    Zhu, Lin; Tang, Xuexi; Wang, Ying; Sui, Yadong; Xiao, Hui

    2016-03-01

    The typical organic pollutant polycyclic aromatic hydrocarbon (PAH) anthracene was selected as a contaminant to investigate its effects on the activities of superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GSH-Px) in the clam Ruditapes philippinarum. The results show that SOD, CAT and GSH-Px had diff erent induction and inhibition reactions to anthracene stress, and that three diff erent organs in R. philippinarum (visceral mass, muscle tissue and mantle) had diff erent sensitivities to anthracene stress. This study suggest that SOD activities of the visceral mass, CAT activitities of the mantle and the visceral mass, and GSH-Px activity of the muscle tissue could be used as sensitive indicators of anthracene stress in R. philippinarum.

  14. Occurrence of polycyclic aromatic hydrocarbons (PAHs) in seawater from the Western Taiwan Strait, China.

    PubMed

    Wu, Yu-Ling; Wang, Xin-Hong; Li, Yong-Yu; Hong, Hua-Sheng

    2011-01-01

    Seawater samples (including surface water and bottom water) were collected from the Western Taiwan Strait (WTS) during June 24-25, 2009; polycyclic aromatic hydrocarbons (PAHs) in dissolved phase and particulate phase were analyzed, respectively. The results showed that the total concentrations of PAHs in the dissolved phase and particulate phase were ranged from 12.3 to 58.0 ng L(-1), and 10.3-45.5 ng L(-1), which showed a low-middle contamination level in the China Seas. The spatial variability of PAHs may be related to the complicated currents of WTS, especially the Min-Zhe coastal current. PAHs diagnostic ratios suggested that PAHs mainly originated from the inputs of pyrolytic (combustion) sources, which might be contributed to land-based atmospheric deposition. The particle-water partition coefficients of individual PAH showed that partitions were not correlated with suspended particulate matter content, dissolved organic carbon or salinity, similar to the Yangtze coastal area.

  15. Deuterium enrichment of polycyclic aromatic hydrocarbons by photochemically induced exchange with deuterium-rich cosmic ices

    NASA Technical Reports Server (NTRS)

    Sandford, S. A.; Bernstein, M. P.; Allamandola, L. J.; Gillette, J. S.; Zare, R. N.

    2000-01-01

    The polycyclic aromatic hydrocarbon (PAH) coronene (C24H12) frozen in D2O ice in a ratio of less than 1 part in 500 rapidly exchanges its hydrogen atoms with the deuterium in the ice at interstellar temperatures and pressures when exposed to ultraviolet radiation. Exchange occurs via three different chemical processes: D atom addition, D atom exchange at oxidized edge sites, and D atom exchange at aromatic edge sites. Observed exchange rates for coronene (C24H12)-D2O and d12-coronene (C24D12)-H2O isotopic substitution experiments show that PAHs in interstellar ices could easily attain the D/H levels observed in meteorites. These results may have important consequences for the abundance of deuterium observed in aromatic materials in the interstellar medium and in meteorites. These exchange mechanisms produce deuteration in characteristic molecular locations on the PAHs that may distinguish them from previously postulated processes for D enrichment of PAHs.

  16. Modeling the unidentified infrared emission with combinations of polycyclic aromatic hydrocarbons

    NASA Technical Reports Server (NTRS)

    Allamandola, L. J.; Hudgins, D. M.; Sandford, S. A.

    1999-01-01

    The infrared emission band spectrum associated with many different interstellar objects can be modeled successfully by using combined laboratory spectra of neutral and positively charged polycyclic aromatic hydrocarbons (PAHs). These model spectra, shown here for the first time, alleviate the principal spectroscopic criticisms previously leveled at the PAH hypothesis and demonstrate that mixtures of free molecular PAHs can indeed account for the overall appearance of the widespread interstellar infrared emission spectrum. Furthermore, these models give us insight into the structures, stabilities, abundances, and ionization balance of the interstellar PAH population. These, in turn, reflect conditions in the emission zones and shed light on the microscopic processes involved in the carbon nucleation, growth, and evolution in circumstellar shells and the interstellar medium.

  17. Investigation of the Reactions and Distribution of Polycyclic Aromatic Hydrocarbons and Fullerenes in Extraterrestrial Material

    NASA Technical Reports Server (NTRS)

    Zare, Richard N.

    2005-01-01

    The work funded by this research grant includes four specific projects: (1) Mapping the spatial distribution of polycyclic aromatic hydrocarbons (PAHs) in a variety of meteoritic samples and comparing this distribution with mineralogical features of the meteorite to determine whether a correlation exists between the two. (2) Developing a method for detection of fullerenes in extraterrestrial samples using microprobe laser-desorption laser-ionization mass spectrometry ( pL2MS) and utilizing this technique to investigate fullerene presence, while exploring the possibility of spatially mapping the fullerene distribution in these samples through in situ detection. (3) Investigating a possible formation pathway for meteoritic and ancient terrestrial kerogen involving the photochemical reactions of PAHs with alkanes under prebiotic and astrophysically relevant conditions. (4) Studying reaction pathways and identifying the photoproducts generated during the photochemical evolution of PAH-containing interstellar ice analogs as part of an ongoing collaboration with researchers at the Astrochemistry Lab at NASA Ames.

  18. Formation of H{sub 2} from internally heated polycyclic aromatic hydrocarbons: Excitation energy dependence

    SciTech Connect

    Chen, T. E-mail: henning@fysik.su.se; Gatchell, M.; Stockett, M. H.; Schmidt, H. T.; Cederquist, H.; Zettergren, H. E-mail: henning@fysik.su.se; Delaunay, R.; Rousseau, P.; Adoui, L.; Domaracka, A.; Huber, B. A.; Tielens, A. G. G. M.

    2015-04-14

    We have investigated the effectiveness of molecular hydrogen (H{sub 2}) formation from Polycyclic Aromatic Hydrocarbons (PAHs) which are internally heated by collisions with keV ions. The present and earlier experimental results are analyzed in view of molecular structure calculations and a simple collision model. We estimate that H{sub 2} formation becomes important for internal PAH temperatures exceeding about 2200 K, regardless of the PAH size and the excitation agent. This suggests that keV ions may effectively induce such reactions, while they are unlikely due to, e.g., absorption of single photons with energies below the Lyman limit. The present analysis also suggests that H{sub 2} emission is correlated with multi-fragmentation processes, which means that the [PAH-2H]{sup +} peak intensities in the mass spectra may not be used for estimating H{sub 2}-formation rates.

  19. Food heating and the formation of heterocyclic aromatic amine and polycyclic aromatic hydrocarbon mutagens/carcinogens.

    PubMed

    Knize, M G; Salmon, C P; Pais, P; Felton, J S

    1999-01-01

    Heterocyclic aromatic amines (HAA) and polycyclic aromatic hydrocarbons (PAH) are mutagens and animal carcinogens sometimes formed when foods are heated or processed. Determining their role in cancer etiology depends on comparing human exposures and determining any significant dose-related effects. Chemical analysis of foods shows that flame-grilling can form both PAH and HAA, and that frying forms predominantly HAA. With detection limits of about 0.1 ng/g, amounts found in commercially processed or restaurant foods range from 0.1 to 14 ng/g for HAA, and levels of PAH up to 1 ng/g in a liquid smoke flavoring. Laboratory fried samples have greater amounts of PAH, up to 38 ng/g in hamburgers, and high levels of HAA, over 300 ng/g, are measured in grilled chicken breast. Understanding the processing conditions that form PAH and HAA can lead to methods to greatly reduce their occurrence in processed foods.

  20. Concentration and particle size distribution of polycyclic aromatic hydrocarbons formed by thermal cooking.

    PubMed

    Saito, E; Tanaka, N; Miyazaki, A; Tsuzaki, M

    2014-06-15

    The concentration and particle size distribution of 19 major polycyclic aromatic hydrocarbons (PAHs) emitted by thermal cooking were investigated. Corn, trout, beef, prawns, and pork were selected for grilling. The PAHs in the oil mist emitted when the food was grilled were collected according to particle size range and analysed by GC/MS. Much higher concentrations of PAHs were detected in the oil mist emitted by grilled pork, trout, and beef samples, which were rich in fat. The main components of the cooking exhaust were 3- and 4-ring PAHs, regardless of food type. The particle size distribution showed that almost all the PAHs were concentrated in particles with diameters of <0.43 μm. For pork, the toxic equivalent of benzo[a]pyrene accounted for 50% of the PAHs in particles with diameters of <0.43 μm. From these results, we estimated that >90% of the PAHs would reach the alveolar region of the lungs.

  1. Study of nitro-polycyclic aromatic hydrocarbons in fine and coarse atmospheric particles

    NASA Astrophysics Data System (ADS)

    Teixeira, Elba Calesso; Garcia, Karine Oliveira; Meincke, Larissa; Leal, Karen Alam

    2011-08-01

    The purpose of the present study was to evaluate six nitro-polycyclic aromatic hydrocarbons (NPAHs) in fine (< 2.5 μm) and coarse (2.5-10 μm) atmospheric particles in an urban and industrial area located in the Metropolitan Area of Porto Alegre (MAPA), RS, Brazil. The method used was of NPAHs isolation and derivatization, and subsequent gas chromatography by electron capture detection (CG/ECD). Results revealed a higher concentration of NPAHs, especially 3-nitrofluoranthene and 1-nitropyrene, in fine particles in the sampling sites studied within the MAPA. The diagnostic ratios calculated for PAHs and NPAHs identified the influence of heavy traffic, mainly of diesel emissions. The correlation of NPAHs with other pollutants (NO x, NO 2, NO and O 3) evidence the influence of vehicular emissions in the MAPA. The seasonal variation evidenced higher NPAHs concentrations in the fine particles during winter for most compounds studied.

  2. SPE-LC-FD determination of polycyclic aromatic hydrocarbon monohydroxy derivatives in cephalopods.

    PubMed

    Lourenço, Diana; Silva, Liliana J G; Lino, Celeste M; Morais, Simone; Pena, Angelina

    2014-03-26

    A new analytical methodology, based on liquid chromatography with fluorescence detection (LC-FD), after extraction, enzymatic hydrolysis, and solid-phase extraction (SPE) through Oasis HLB cartridges, was developed and validated for the simultaneous determination of three monohydroxy derivatives of polycyclic aromatic hydrocarbons (PAHs). The optimized analytical method is sensitive, accurate, and precise, with recoveries between 62 and 110% and limits of detection of 227, 9, and 45 ng/g for 1-hydroxynaphthalene, 2-hydroxyfluorene, and 1-hydroxypyrene, respectively. Their levels were estimated in different cephalopod matrices (edible tissues and hemolymph). The methodology was applied to samples of the major cephalopod species consumed worldwide. Of the 18 samples analyzed, 39% were contaminated with 1-hydroxynaphthalene, which was the only PAH metabolite detected. Its concentration ranged from 786 to 1145 ng/g. This highly sensitive and specific method allows the identification and quantitation of PAH metabolites in forthcoming food safety and environmental monitoring programs.

  3. Atmospheric polycyclic aromatic hydrocarbons in the urban environment: Occurrence, toxicity and source apportionment.

    PubMed

    Mishra, Nitika; Ayoko, Godwin A; Morawska, Lidia

    2016-01-01

    Polycyclic Aromatic Hydrocarbons (PAHs) represent a major class of toxic pollutants because of their carcinogenic and mutagenic characteristics. People living in urban areas are regularly exposed to PAHs because of abundance of their emission sources. Within this context, this study aimed to: (i) identify and quantify the levels of ambient PAHs in an urban environment; (ii) evaluate their toxicity; and (iii) identify their sources as well as the contribution of specific sources to measured concentrations. Sixteen PAHs were identified and quantified in air samples collected from Brisbane. Principal Component Analysis - Absolute Principal Component Scores (PCA-APCS) was used in order to conduct source apportionment of the measured PAHs. Vehicular emissions, natural gas combustion, petrol emissions and evaporative/unburned fuel were the sources identified; contributing 56%, 21%, 15% and 8% of the total PAHs emissions, respectively, all of which need to be considered for any pollution control measures implemented in urban areas.

  4. Flow cytometry detection of planktonic cells with polycyclic aromatic hydrocarbons sorbed to cell surfaces.

    PubMed

    Cerezo, Maria I; Linden, Matthew; Agustí, Susana

    2017-02-17

    Polycyclic aromatic hydrocarbons are very important components of oil pollution. These pollutants tend to sorb to cell surfaces, exerting toxic effects on organisms. Our study developed a flow cytometric method for the detection of PAHs sorbed to phytoplankton by exploiting their spectral characteristics. We discriminated between cells with PAHs from cells free of PAHs. Clear discrimination was observed with flow cytometer provided with 375 or 405nm lasers in addition to the standard 488nm laser necessary to identify phytoplankton. Using this method, we measured the relationship between the percentages of phytoplankton organisms with PAHs, with the decrease in the growth rate. Moreover, the development of this method could be extended to facilitate the study of PAHs impact on cell cultures from a large variety of organisms.

  5. Polycyclic aromatic hydrocarbon pollution in the surface water and sediments of Chabahar Bay, Oman Sea.

    PubMed

    Agah, Homira; Mehdinia, Ali; Bastami, Kazem Darvish; Rahmanpour, Shirin

    2017-02-15

    In the present study, the concentrations and distribution of 16 polycyclic aromatic hydrocarbons (PAHs) in the water and surface sediments from the Chabahar Bay, Oman Sea, were investigated in May (premonsoon) and December (postmonsoon) 2012. The concentrations of PAHs in the surface water samples ranged from 1.7 to 2.8ngl(-1) and from 0.04 to 59.6ngl(-1) in pre- and postmonsoon, respectively. In general, the PAH levels of the water samples from Chabahar Bay were higher in postmonsoon than in premonsoon (p<0.05). The concentrations of PAHs in the sediment samples varied from undetectable levels to 92.8ngg(-1) d.w. in both seasons. The seasonal comparison of the results in sediment samples showed that the overall concentration of PAH compounds was higher in the postmonsoon season (p<0.05).

  6. Gas-phase Reactions of Polycyclic Aromatic Hydrocarbon Anions with Molecules of Interstellar Relevance

    NASA Astrophysics Data System (ADS)

    Demarais, Nicholas J.; Yang, Zhibo; Martinez, Oscar; Wehres, Nadine; Snow, Theodore P.; Bierbaum, Veronica M.

    2012-02-01

    We have studied reactions of small dehydrogenated polycyclic aromatic hydrocarbon anions with neutral species of interstellar relevance. Reaction rate constants are measured at 300 K for the reactions of phenide (C6H- 5), naphthalenide (C10H- 7), and anthracenide (C14H- 9) with atomic H, H2, and D2 using a flowing afterglow-selected ion flow tube instrument. Reaction rate constants of phenide with neutral molecules (CO, O2, CO2, N2O, C2H2, CH3OH, CH3CN, (CH3)2CO, CH3CHO, CH3Cl, and (CH3CH2)2O) are also measured under the same conditions. Experimental measurements are accompanied by ab initio calculations to provide insight into reaction pathways and enthalpies. Our measured reaction rate constants should prove useful in the modeling of astrophysical environments, particularly when applied to dense regions of the interstellar and circumstellar medium.

  7. An unexpected restructuring of combustion soot aggregates by subnanometer coatings of polycyclic aromatic hydrocarbons

    NASA Astrophysics Data System (ADS)

    Chen, Chao; Fan, Xiaolong; Shaltout, Tasneem; Qiu, Chong; Ma, Yan; Goldman, Andrew; Khalizov, Alexei F.

    2016-10-01

    We investigated the effect of thin polycyclic aromatic hydrocarbon (PAH) coatings on the structure of soot aggregates. Soot aerosol from an inverted diffusion burner was size classified, thermally denuded, coated with six different PAHs, and then characterized using scanning electron microscopy, light scattering, and mass-mobility measurements. Contrary to our expectation, significant restructuring was observed in the presence of subnanometer layers of pyrene, fluoranthene, and phenanthrene. These PAHs remained in subcooled liquid state in thin films, whereby the liquid layer acted as a lubricant, reducing the force required to initiate the restructuring. Thin layers of PAH of higher melting temperatures (perylene, anthracene, and triphenylene) presumably remained solid because these chemicals induced lesser structural changes. Our results suggest that some of the intrinsic PAH generated during incomplete combustion may induce significant restructuring of soot aggregates, even when present in small quantities, altering the properties and atmospheric impacts of combustion aerosols.

  8. Determination of polycyclic aromatic hydrocarbons in kerosene and bio-kerosene soot.

    PubMed

    Andrade-Eiroa, Auréa; Leroy, Valérie; Dagaut, Philippe; Bedjanian, Yuri

    2010-03-01

    Here we report a new, efficient and reliable analytical methodology for sensitive and selective quantification of Polycyclic Aromatic Hydrocarbons (PAHs) in soot samples. The methodology developed is based on ultrasonic extraction of the soot-bound PAHs into small volumes of acetonitrile, purification of the extracts through C(18) Solid Phase Extraction (SPE) cartridges and analysis by Reverse Phase Liquid Chromatography (RPLC) with UV and fluorimetric detection. For the first time, we report the convenience of adapting the SPE procedure to the nature of the soot samples. As a matter of fact, extracts containing high percentage of unpolar material are recommended to be cleaned with acetone, whereas extracts poor in unpolar compounds can be efficiently cleaned with methanol. The method was satisfactorily applied to kerosene and bio-kerosene soot from atmospheric open diffusion flames (pool fires) and premixed flames achieving Quantification and Detection limits in the range ng mg(-1) soot and recoveries about 90% for most of the PAHs studied.

  9. Use of constant wavelength synchronous spectrofluorimetry for identification of polycyclic aromatic hydrocarbons in air particulate samples

    NASA Astrophysics Data System (ADS)

    Sharma, Homdutt; Jain, V. K.; Khan, Zahid H.

    2013-05-01

    We have developed a simple, rapid, inexpensive method for the identification of fluoranthene (Flan), benz(a)anthracene (BaA), benzo(a)pyrene (BaP), benzo(k)fluoranthene (BkF), pyrene (Pyr), benz(ghi)perylene (BghiP) in suspended particulate matter in an urban environment of Delhi. Suspended particulate matter samples of 24 h duration were collected on glass fiber filter papers. Polycyclic aromatic hydrocarbons (PAHs) were extracted from the filter papers using dichloromethane (DCM) and hexane with ultrasonication method. Comparison of the characteristic emission of spectra of PAHs with standard spectra indicated the degree of condensation of aromatic compounds present in investigated mixtures. It was also possible to identify some individual compounds. However, this identification could be more effective with the use of the respective values of Δλ parameter for each particular component of the mixture.

  10. Fast Screening of Polycyclic Aromatic Hydrocarbons using Trapped Ion Mobility Spectrometry - Mass Spectrometry

    PubMed Central

    Castellanos, A.; Benigni, P.; Hernandez, D. R.; DeBord, J. D.; Ridgeway, M. E.; Park, M. A.

    2014-01-01

    In the present paper, we showed the advantages of trapped ion mobility spectrometry coupled too mass spectrometry (TIMS-MS) combined with theoretical calculations for fast identification (millisecond timescale) of polycyclic aromatic hydrocarbons (PAH) compounds from complex mixtures. Accurate PAH collision cross sections (CCS, in nitrogen as a bath gas) are reported for the most commonly encountered PAH compounds and the ability to separate PAH geometric isomers is shown for three isobaric pairs with mobility resolution exceeding 150 (3–5 times higher than conventional IMS devices). Theoretical candidate structures (optimized at the DFT/B3LYP level) are proposed for the most commonly encountered PAH compounds showing good agreement with the experimental CCS values (<5%). The potential of TIMS-MS for the separation and identification of PAH compounds from complex mixtures without the need of lengthy pre-separation steps is illustrated for the case of a complex soil mixture. PMID:25558291

  11. Polycyclic aromatic hydrocarbons in deep sea sediments: Microbe-pollutant interactions in a remote environment.

    PubMed

    Louvado, A; Gomes, N C M; Simões, M M Q; Almeida, A; Cleary, D F R; Cunha, A

    2015-09-01

    Recalcitrant polycyclic aromatic hydrocarbons (PAHs) released into seawater end up in the deep sea sediments (DSSs). However, their fate here is often oversimplified by theoretical models. Biodegradation of PAHs in DSSs, is assumed to be similar to biodegradation in surface habitats, despite high hydrostatic pressures and low temperatures that should significantly limit PAH biodegradation. Bacteria residing in the DSSs (related mainly to α- and γ-Proteobacteria) have been shown to or predicted to possess distinct genes, enzymes and metabolic pathways, indicating an adaptation of these bacterial communities to the psychro-peizophilic conditions of the DSSs. This work summarizes some of the most recent research on DSS hydrocarbonoclastic populations and mechanisms of PAH degradation and discusses the challenges posed by future high CO2 and UV climate scenarios on biodegradation of PAHs in DSSs.

  12. Parking lot sealcoat: an unrecognized source of urban polycyclic aromatic hydrocarbons

    SciTech Connect

    Barbara J. Mahler; Peter C. Van Metre; Thomas J. Bashara; Jennifer T. Wilson; David A. Johns

    2005-08-01

    Polycyclic aromatic hydrocarbons (PAHs) are a ubiquitous contaminant in urban environments. Although numerous sources of PAHs to urban runoff have been identified, their relative importance remains uncertain. The authors show that a previously unidentified source of urban PAHs, parking lot sealcoat, may dominate loading of PAHs to urban water bodies in the United States. Particles in runoff from parking lots with coal-tar emulsion sealcoat had mean concentrations of PAHs of 3500 mg/kg, 65 times higher than the mean concentration from unsealed asphalt and cement lots. Diagnostic ratios of individual PAHs indicating sources are similar for particles from coal-tar emulsion sealed lots and suspended sediment from four urban streams. Contaminant yields projected to the watershed scale for the four associated watersheds indicate that runoff from sealed parking lots could account for the majority of stream PAH loads. 35 refs., 6 figs., 2 tabs.

  13. Emissions of polycyclic aromatic hydrocarbons (PAH) from open burning of biomass

    SciTech Connect

    Jenkins, B.M.

    1995-12-01

    Emissions of polycyclic aromatic hydrocarbons (PAH) were measured during wind tunnel simulations of open burning for various types of biomass. The wind tunnel (Jenkins, et al., 1993) was used to simulate open fires spreading in opposition to the wind for cereal crop residues, and pile fires in agricultural and sylvicultural wood residues. Emission factors expressing the mass of pollutant species emitted per unit mass of dry fuel consumed were derived from mass balances conducted on each fire. Emission factors for primary pollutants and volatile organic species were similarly derived. Partitioning of PAH in the combustion products was investigated by determining mass fractions on particulate matter and in a downstream resin trap and other sampling train components. Yields of PAH are given for the major types of fuels and burning conditions.

  14. Evaluation of models for predicting the phototoxicity potency of polycyclic aromatic hydrocarbons

    SciTech Connect

    Erickson, R.J.; Ankley, G.T.; Sheedy, B.R.; Kosian, P.A.; Mattson, V.R.; Cox, J.S.; Defoe, D.L.

    1995-12-31

    The acute phototoxicities of selected polycyclic aromatic hydrocarbons (PAHs) to the oligochaete Lumbriculus variegatus were investigated in order to evaluate a predictive structure/activity relationship (SAR) for the phototoxic potential of PAHs and to determine the relationship of phototoxicity to PAH accumulation, light intensity, and exposure duration. Test organisms were exposed to multiple concentrations of anthracene, pyrene, fluorene, and fluoranthene in water for 96 h and then to various intensities of ultraviolet light for 96 h in clean water. In agreement with the SAR model, fluorene was not phototoxic while pyrene, fluoranthene, and anthracene were. Based upon measured accumulations of PAHs, anthracene and pyrene had similar potencies, and both were 3--4 fold more toxic than fluoranthene. Time-to-death was found to adhere well to a model based on damage accumulating as a function of the product of chemical accumulation and light intensity. Additivity of PAH phototoxicity was evaluated in exposures using mixtures of these chemicals.

  15. The effect of humic acids on biodegradation of polycyclic aromatic hydrocarbons depends on the exposure regime.

    PubMed

    Tejeda-Agredano, Maria-Carmen; Mayer, Philipp; Ortega-Calvo, Jose-Julio

    2014-01-01

    Binding of polycyclic aromatic hydrocarbons (PAHs) to dissolved organic matter (DOM) can reduce the freely dissolved concentration, increase apparent solubility or enhance diffusive mass transfer. To study the effects of DOM on biodegradation, we used phenanthrene and pyrene as model PAHs, soil humic acids as model DOM and a soil Mycobacterium strain as a representative degrader organism. Humic acids enhanced the biodegradation of pyrene when present as solid crystals but not when initially dissolved or provided by partitioning from a polymer. Synchronous fluorescence spectrophotometry, scintillation counting and a microscale diffusion technique were applied in order to determine the kinetics of dissolution and diffusive mass transfer of pyrene. We suggest that humic acids can enhance or inhibit biodegradation as a result of the balance of two opposite effects, namely, solubilization of the chemicals on the one hand and inhibition of cell adhesion to the pollutant source on the other.

  16. Microbial community dynamics and biodegradation of polycyclic aromatic hydrocarbons in polluted marine sediments in Hong Kong.

    PubMed

    Wang, Y F; Tam, N F Y

    2011-01-01

    Dynamics of microbial community and biodegradation of polycyclic aromatic hydrocarbons (PAHs) in polluted marine sediments, artificially spiked with a mixture of PAHs (fluorene, phenanthrene, fluoranthene and pyrene), were examined for a period of 60 days. Microbial communities were characterised by bacterial counts, ester-linked fatty acid methyl ester (EL-FAME) analysis and denaturing gradient gel electrophoresis (DGGE). A noted reduction in species diversity occurred only in the high PAH level treatment at onset. Both EL-FAME and DGGE demonstrated a marked shift in microbial community, in all the PAH level treatments, afterwards, with increases in the number of fatty acid degraders, the relative abundance of fatty acid biomarkers for gram-negative bacteria and a decrease in species diversity. The shift was also accompanied by the significant decrease in PAH concentrations. By the end of the experiment, diversity indices, based on both approaches, recovered when PAH concentrations declined to their background levels, except in the high PAH level treatment.

  17. In situ evaluations of storm water toxicity due polycyclic aromatic hydrocarbons associated with particulate matter

    SciTech Connect

    Ireland, D.S.; Burton, G.A. Jr.

    1994-12-31

    Polycyclic aromatic hydrocarbons (PAHs) are widespread pollutants that enter the aquatic environment from many anthropogenic sources, as well as natural sources, and have been shown to cause a wide range of toxic effects in freshwater and marine organisms. PAHs are subject to photomodification by ultraviolet (UV) radiation to more water soluble and more toxic forms. In situ chambers containing Ceriodaphnia dubia were used to observe this phenomenon. These chambers were placed in a stream contaminated with PAHs. These chambers were placed in area shielded and exposed to UV wavelengths. Toxicity is only shown when UV wavelengths are able to penetrate the water column. Chemical analysis reveals that the majority of the PAHs present are associated with particulate matter. Chemical analysis of the sediment reveals PAH levels much higher than that of the water column. The level of PAHs associated with suspended matter increases during a storm event. This basic test supports the phototoxicity of PAHs associated with particulate matter.

  18. Geochemistry of polycyclic aromatic hydrocarbons in Columbia River and Washington coastal sediments

    SciTech Connect

    Prahl, F.G.

    1982-01-01

    A field investigation was conducted to determine the origins, dispersal pathways and fates of polycyclic aromatic hydrocarbons (PAH) in a river-influenced coastal marine environment. The complex PAH mixtures found in Washington coastal sediments are derived from several land-based sources. PAH products from anthropogenic combustion processes and two natural PAH, retene and perylene, are the dominant components of these complex mixtures. A natural series of phenanthrene homologs and series of tetracyclic PAH geochemically analogous to retene are present as minor constituents. The three major PAH types in Washington coastal sediments are enriched in a narrow band of coarse silt sediment, extending northwestward from the river mouth to Quinault canyon. The natural phenanthrene series is preferentially advected offshore and deposited. These distributions are consistent with known PAH-particle associations and transport processes influencing sediment dispersal in this coastal environment. Dated sediment core records suggest this PAH dispersal pattern has persisted for at least the past century.

  19. Non-destructive assessment of polycyclic aromatic hydrocarbon (PAH) exposure by fluorimetric analysis of crab urine.

    PubMed

    Koenig, Samuel; Savage, Candida; Kim, Jonathan P

    2008-12-01

    The detection of urinary polycyclic aromatic hydrocarbon (PAH) metabolites by fluorescence spectrophotometry is particularly effective as a practical means to assess PAH exposure in decapod crabs. However, the practical application of this technique has thus far only been tested for the European shore crab (Carcinus maenas) and only a few field studies have been conducted in heavily polluted areas. The present study evaluated the adaptability of this method as a rapid, cost-effective and non-destructive biomonitoring tool for the New Zealand crab species, Macrophthalmus hirtipes (stalk-eyed mud crab). A field gradient could be detected among the sites and different input sources of PAH contamination could be discerned through the differentiation of pyrogenic and petrogenic PAH signatures. The present study shows that the fluorescence screening method is sensitive to relatively low levels of PAH contamination and more broadly applicable to smaller crab species than C. maenas, for which the technique was developed.

  20. Baseline values of Polycyclic Aromatic Hydrocarbons and Trace Metals in the Yukon River, Alaska

    NASA Astrophysics Data System (ADS)

    Perreault, J.; McCarthy, P.

    2014-12-01

    The Yukon River drains an area of more than 800 km2 across Canada and Alaska. Sediments are deposited along the western coast of Alaska in the Bering and Chukchi Seas, and represent most of the sediment deposited in the Chukchi Sea. Suspended sediments, bed load sediments, and historical cores were collected from the last non-marine influenced stretch of the Yukon River and analyzed for the presence and quantity of trace metals, organic carbon, and polycyclic aromatic hydrocarbons (PAH). C14 dates from cores sampled from the delta region and intra-annual active river sampling from 2012-2013, show an annual flux of these materials within the context of a historical comparison. Grain size distributions of tested contaminants suggest contributions to the Chukchi Sea sediment budget.

  1. Baseline values of Polycyclic Aromatic Hydrocarbons and Trace Metals in the Yukon River sediments, Alaska

    NASA Astrophysics Data System (ADS)

    Perreault, J.

    2015-12-01

    The Yukon River drains an area of more than 800 km2 across Canada and Alaska and sediments are deposited along the western coast of Alaska in the Bering and Chukchi Seas, and represent most of the sediment deposited in the Chukchi Sea. Suspended sediments, bed load sediments, and historical cores were collected from the last non-marine influenced stretch of the Yukon River and analyzed for the presence and quantity of trace metals, organic carbon, and polycyclic aromatic hydrocarbons (PAH). With C14 dates from cores sampled from the delta region and intra-annual active river sampling from 2012-2013, some variation will show an annual flux of these materials with a historical comparison. Results of grain size distribution of tested contaminants will suggest contributions to the Chukchi Sea sediment budget.

  2. Removal of polycyclic aromatic hydrocarbons in aqueous environment by chemical treatments: a review.

    PubMed

    Rubio-Clemente, Ainhoa; Torres-Palma, Ricardo A; Peñuela, Gustavo A

    2014-04-15

    Due to their carcinogenic, mutagenic and teratogenic potential, the removal of polycyclic aromatic hydrocarbons (PAHs) from aqueous environment using physical, biological and chemical processes has been studied by several researchers. This paper reviews the current state of knowledge concerning PAHs including their physico-chemical properties, input sources, occurrence, adverse effects and conventional and alternative chemical processes applied for their removal from water. The mechanisms and reactions involved in each treatment method are reported, and the effects of various variables on the PAH degradation rate as well as the extent of degradation are also discussed. Extensive literature analysis has shown that an effective way to perform the conversion and mineralization of this type of substances is the application of advanced oxidation processes (AOPs). Furthermore, combined processes, particularly AOPs coupled with biological treatments, seem to be one of the best solutions for the treatment of effluents containing PAHs.

  3. Effect of beer marinades on formation of polycyclic aromatic hydrocarbons in charcoal-grilled pork.

    PubMed

    Viegas, Olga; Yebra-Pimentel, Iria; Martínez-Carballo, Elena; Simal-Gandara, Jesus; Ferreira, Isabel M P L V O

    2014-03-26

    The effect of marinating meat with Pilsner beer, nonalcoholic Pilsner beer, and Black beer (coded respectively PB, P0B, and BB) on the formation of polycyclic aromatic hydrocarbons (PAHs) in charcoal-grilled pork was evaluated and compared with the formation of these compounds in unmarinated meat. Antiradical activity of marinades (DPPH assay) was assayed. BB exhibited the strongest scavenging activity (68.0%), followed by P0B (36.5%) and PB (29.5%). Control and marinated meat samples contained the eight PAHs named PAH8 by the EFSA and classified as suitable indicators for carcinogenic potency of PAHs in food. BB showed the highest inhibitory effect in the formation of PAH8 (53%), followed by P0B (25%) and PB (13%). The inhibitory effect of beer marinades on PAH8 increased with the increase of their radical-scavenging activity. BB marinade was the most efficient on reduction of PAH formation, providing a proper mitigation strategy.

  4. Characterizing the parent and oxygenated polycyclic aromatic hydrocarbons in mangrove sediments of Hong Kong.

    PubMed

    Wang, Xiaowei; Yuan, Ke; Yang, Lihua; Lin, Li; Tam, Nora F Y; Chen, Baowei; Luan, Tiangang

    2015-09-15

    Parent and oxygenated polycyclic aromatic hydrocarbons (PAHs) were investigated in mangrove sediments of Hong Kong. Most of the analytes were detected, and the dominant carbonylic and hydroxylated PAHs in mangrove sediments were 9-fluorenone and 2-hydroxy fluorene, respectively. The concentration of 9-fluorenone and 9,10-anthraquinone was higher than their parent PAHs. Moreover, the concentration of total organic matter (TOM) related with those of the parent PAHs and carbonylic PAHs, except for hydroxylated PAHs, which indicated that TOM was not the only factor regulating the distribution of oxygenated PAHs. Nevertheless, the parent PAHs in mangrove sediments was correlated positively with carbonylic PAHs which demostrated not only the similar source but also the fate of these two compound class. However, hydroxylated PAHs had different source by comparing with parent PAHs and carbonylic PAHs, they were probably originated from biodegradation and accumulated in mangrove sediments.

  5. Degradation of polycyclic aromatic hydrocarbons by a marine fluidized-bed enrichment

    SciTech Connect

    Melin, E.S.; Puhakka, J.A.; Maennistoe, M.; Ferguson, J.F.

    1995-12-31

    Aerobic polycyclic aromatic hydrocarbon (PAH)-degrading bacteria from marine sediments were enriched and maintained in a fluidized-bed reactor (FBR). The FBR was continuously fed a mixture of naphthalene, biphenyl, 2-methylnaphthalene, 2,6-dimethylnaphthalene, acenaphthene, fluorene, and phenanthrene; and the effluent concentrations remained below 0.03 mg/L (detection limit) over a period of 6 months. In batch vial assays, the relative rates of PAH degradation were controlled by their solubilities and, in some cases, by their substitution patterns. The enrichment also degraded several other PAHs, including anthracene and pyrene. The results demonstrate that the predominant PAH constituents of coal-tar creosote can be degraded and that PAH-contaminated saline waters can be remediated by the marine enrichment.

  6. Degradation of Polycyclic Aromatic Hydrocarbons (PAHs) by Bacteria Isolated from Light Oil Polluted Soils

    NASA Astrophysics Data System (ADS)

    Ohnuma, T.; Suto, K.; Inoue, C.

    2007-03-01

    Polycyclic aromatic hydrocarbons (PAHs) have polluted soil and groundwater widely and for long term because of their low solubility at normal temperature. Several microorganisms, such as Pseudomonas sp., Sphigomonas sp., a white-rot fungus and so on, being able to decompose PAHs, have been isolated and researched. This study reported to investigate biodegradation of low molecule PAH by isolated bacteria from light oil polluted soil. 12 isolates were obtained from a light oil polluted soil using naphthalene, fluorene and anthracene as sole carbon source, of which 4 isolates grew with naphthalene, 4 isolates did with fluorene and 4 isolates did with anthracene. Among them 3 isolates showed the ability to degrade phenanthrene additionally. These phenanthrene degradation and growth rates were almost same as that of S. yanoikuyae (DSM6900), which is the typical bacteria of PAHs degrader. Therefore, the isolate seemed to have an expectation for PAHs degradation.

  7. Combined chemical and biological oxidation of slurry phase polycyclic aromatic hydrocarbons

    SciTech Connect

    Brown, K.L.; Davila, B.; Sanseverino, J.; Thomas, M.; Lang, C.

    1995-07-01

    Bioslurry treatment of polycyclic aromatic hydrocarbon (PAH)-impacted soils was demonstrated under the Superfund Innovative Technologies Evaluation (SITE)/Emerging Technologies Program (ETD) as an extension of research previously funded by IT Corporation (IT) and additional investigations supported by the U.S. Environmental Protection Agency (EPA). During the demonstration, IT operated two 60-liter (L) TEKNO Associates bioslurry reactors (Salt Lake City, Utah) and a 10-L fermentation unit is semicontinuous, plug-flow mode for a 2-month period. The first 60-L reactor received fresh feed daily and supplements of salcylate and succinate to enhance PAH degradation. During operation, the bioslurry reactor system demonstrated average PAH and carcinogenic PAH (CPAH) removals of 84 and 66 percent, respectively. The reactors will be operated over the next four months to increase the rate and extent of PAH biodegradation. The objective of the demonstration is to illustrate bioslurry treatment of impacted soils and sludges as an effective and economically attractive remedial option.

  8. POLYCYCLIC AROMATIC HYDROCARBONS WITH ARMCHAIR EDGES AND THE 12.7 μm BAND

    SciTech Connect

    Candian, A.; Tielens, A. G. G. M.; Sarre, P. J.

    2014-08-10

    In this Letter, we report the results of density functional theory calculations on medium-sized neutral polycyclic aromatic hydrocarbon (PAH) molecules with armchair edges. These PAH molecules possess strong C-H stretching and bending modes around 3 μm and in the fingerprint region (10-15 μm), and also strong ring deformation modes around 12.7 μm. Perusal of the entries in the NASA Ames PAHs Database shows that ring deformation modes of PAHs are common, although generally weak. Therefore, we propose that armchair PAHs with N{sub C} > 65 are responsible for the 12.7 μm aromatic infrared band in H II regions and discuss the astrophysical implications in the context of the PAH life cycle.

  9. Determination of polycyclic aromatic hydrocarbon (PAH) content and risk assessment from edible oils in Korea.

    PubMed

    Kang, Bomi; Lee, Byung-Mu; Shin, Han-Seung

    2014-01-01

    Polycyclic aromatic hydrocarbons (PAH) content and a risk assessment from consumption of Korean edible oils were investigated. Liquid-liquid extraction and gas chromatography-mass spectroscopy were used to measure eight PAH in edible oils commonly consumed in Korea. The total average PAH concentration was 0.548 μg/kg from edible oils and the content of the 8 PAH was lower than 2 μg/kg, which is the maximum tolerable limit reported by the commission regulation. The contents of the eight PAH were converted to exposure assessment and risk characterization values. Dietary exposure to PAH from edible oils was 0.025 ng-TEQBaP/kg/d, and margin of exposure (MOE) was 4 × 10(6), which represents negligible concern. Although PAH were detected from edible oils in Korea, their contribution to human exposure to PAH is considered not significant.

  10. A molecular dynamics study on slow ion interactions with the polycyclic aromatic hydrocarbon molecule anthracene

    SciTech Connect

    Postma, J.; Hoekstra, R.; Schlathölter, T.; Tielens, A. G. G. M.

    2014-03-01

    Atomic collisions with polycyclic aromatic hydrocarbon (PAH) molecules are astrophysically particularly relevant for collision energies of less than 1 keV. In this regime, the interaction dynamics are dominated by elastic interactions. We have employed a molecular dynamics simulation based on analytical interaction potentials to model the interaction of low energy hydrogen and helium projectiles with isolated anthracene (C{sub 14}H{sub 10}) molecules. This approach allows for a very detailed investigation of the elastic interaction dynamics on an event by event basis. From the simulation data the threshold projectile kinetic energies above which direct C atom knock out sets in were determined. Anthracene differential energy transfer cross sections and total (dissociation) cross sections were computed for a wide range of projectile kinetic energies. The obtained results are interpreted in the context of PAH destruction in astrophysical environments.

  11. THE NASA AMES POLYCYCLIC AROMATIC HYDROCARBON INFRARED SPECTROSCOPIC DATABASE: THE COMPUTED SPECTRA

    SciTech Connect

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

    2010-08-15

    The astronomical emission features, formerly known as the unidentified infrared bands, are now commonly ascribed to polycyclic aromatic hydrocarbons (PAHs). The laboratory experiments and computational modeling done at the NASA Ames Research Center to create a collection of PAH IR spectra relevant to test and refine the PAH hypothesis have been assembled into a spectroscopic database. This database now contains over 800 PAH spectra spanning 2-2000 {mu}m (5000-5 cm{sup -1}). These data are now available on the World Wide Web at www.astrochem.org/pahdb. This paper presents an overview of the computational spectra in the database and the tools developed to analyze and interpret astronomical spectra using the database. A description of the online and offline user tools available on the Web site is also presented.

  12. Sorption effects interfering with the analysis of polycyclic aromatic hydrocarbons (PAH) in aqueous samples.

    PubMed

    Krüger, Oliver; Kalbe, Ute; Meißner, Kerstin; Sobottka, Sebastian

    2014-05-01

    Polycyclic aromatic hydrocarbons (PAH) are severe environmental pollutants that are analyzed frequently. The risk assessment of PAH impact to groundwater can be performed using leaching tests. Therby a liquid-solid separation step including centrifugation may be required, which in turn might lead to loss of analytes due to sorption on the equipment. Thus we determined the PAH recoveries from various container materials (polyethylene (PE), polypropylene (PP), polytetraflourethylene (PTFE), stainless steel (ES), and perflouroalkoxy (PFA)) and compared them to selected PAH properties. We found the best recoveries for PFA (68%) and PTFE (65%) containers. We found good negative correlations (-0.93 and better) between PAH recovery and log partition coefficient organic carbon-water (logKOC) for PFA, PTFE, and ES containers.

  13. Parking lot sealcoat: An unrecognized source of urban polycyclic aromatic hydrocarbons

    USGS Publications Warehouse

    Mahler, B.J.; Van Metre, P.C.; Bashara, T.J.; Wilson, J.T.; Johns, D.A.

    2005-01-01

    Polycyclic aromatic hydrocarbons (PAHs) are a ubiquitous contaminant in urban environments. Although numerous sources of PAHs to urban runoff have been identified, their relative importance remains uncertain. We show that a previously unidentified source of urban PAHs, parking lot sealcoat, may dominate loading of PAHs to urban water bodies in the United States. Particles in runoff from parking lots with coal-tar emulsion sealcoat had mean concentrations of PAHs of 3500 mg/kg, 65 times higher than the mean concentration from unsealed asphalt and cement lots. Diagnostic ratios of individual PAHs indicating sources are similar for particles from coal-tar emulsion sealed lots and suspended sediment from four urban streams. Contaminant yields projected to the watershed scale for the four associated watersheds indicate that runoff from sealed parking lots could account for the majority of stream PAH loads. ?? 2005 American Chemical Society.

  14. Gas chromatographic-mass spectrometric method for polycyclic aromatic hydrocarbon analysis in plant biota.

    PubMed

    Meudec, A; Dussauze, J; Jourdin, M; Deslandes, E; Poupart, N

    2006-03-10

    Using gas chromatography-mass spectrometry, a new method was developed for the identification and the quantification of polycyclic aromatic hydrocarbons (PAHs) in plants. This method was particularly optimised for PAH analyses in marine plants such as the halophytic species, Salicornia fragilis Ball et Tutin. The saponification of samples and their clean up by Florisil solid-phase extraction succeeded in eliminating pigments and natural compounds, which may interfere with GC-MS analysis. Moreover, a good recovery of the PAHs studied was obtained with percentages ranging from 88 to 116%. Application to the determination of PAH in a wide range of coastal halophytic plants is presented and validated the efficiency, the accuracy and the reproducibility of this method.

  15. Promising approaches towards biotransformation of polycyclic aromatic hydrocarbons with Ascomycota fungi.

    PubMed

    Aranda, Elisabet

    2016-04-01

    The bioremediation of hazardous aromatic pollutants such as polycyclic aromatic hydrocarbons (PAHs) has been extensively studied in recent decades, including the potential use of different phyla of fungi for this purpose. Molecular technologies are starting to reveal that the real players in polluted environments are mainly represented by the phylum Ascomycota and the subphylum Mucoromycotina and, to a lesser extent, the phylum Basidiomycota. Paradoxically, despite their key involvement, these groups of fungi are often treated as a black box, and their potential roles in the transformation of xenobiotics and catabolic pathways remain poorly understood. The complex intracellular metabolism seems to play a major role in the ability of these fungi to transform or remove PAHs, and their associated enzymes are encoded in the xenome. Functional genomics offers novel information about this enzymatic system, which is widely distributed among all phyla.

  16. In silico bioremediation of polycyclic aromatic hydrocarbon: a frontier in environmental chemistry.

    PubMed

    Librando, Vito; Pappalardo, Matteo

    2013-07-01

    In recent years, the number of studies in the field of bioremediation has been growing steadily. Although a large number of studies provide information that is highly detailed and offer great amounts of knowledge on a given subject, the downside is that the hunt for more information requires the combined efforts of researchers from many areas, which are becoming increasingly difficult to attain. In this review, we present an overview of recent work investigating enzyme degradation of polycyclic aromatic hydrocarbons. In the first part, this review examines several of the new enzymes able to degrade pollutants, with special attention being given to those with a well-resolved structure. The second part explores some of the most recent work in which computational approaches, such as molecular dynamics, docking, density functional theory and database retrieval, have been employed to study enzymes with specific bioremediation activities.

  17. Responses of Chironomus tentans and Hyalella azteca to polycyclic aromatic hydrocarbons

    SciTech Connect

    Hatch, A.C.; Burton, G.A. Jr.

    1995-12-31

    The toxicity of polycyclic aromatic hydrocarbons (PAHs) is affected by ultraviolet (UV) light and a number of interacting environmental variables. The effect of two photoinduced PAHs, anthracene and fluoranthene, was studied with the midge, C. tentans, and the amphipod H. azteca in water-only and sediment exposures. Reduced growth was observed in the presence of UV light at low (ug/L) concentrations. Mixtures showed approximately additive responses. The amphipod was slightly more sensitive to photoinduced toxicity. Responses were modified by exposure differences due to behavior patterns, which altered UV exposures. Results suggest natural factors such as inorganic and organic particulates, in combination with behavior, have a significant role in determining the ecological relevance of photoinduced PAH toxicity.

  18. Polycyclic Aromatic Hydrocarbons in Coastal Sediment of Klang Strait, Malaysia: Distribution Pattern, Risk Assessment and Sources

    PubMed Central

    Tavakoly Sany, Seyedeh Belin; Hashim, Rosli; Salleh, Aishah; Rezayi, Majid; Mehdinia, Ali; Safari, Omid

    2014-01-01

    Concentration, source, and ecological risk of polycyclic aromatic hydrocarbons (PAHs) were investigated in 22 stations from surface sediments in the areas of anthropogenic pollution in the Klang Strait (Malaysia). The total PAH level in the Klang Strait sediment was 994.02±918.1 µg/kg dw. The highest concentration was observed in stations near the coastline and mouth of the Klang River. These locations were dominated by high molecular weight PAHs. The results showed both pyrogenic and petrogenic sources are main sources of PAHs. Further analyses indicated that PAHs primarily originated from pyrogenic sources (coal combustion and vehicular emissions), with significant contribution from petroleum inputs. Regarding ecological risk estimation, only station 13 was moderately polluted, the rest of the stations suffered rare or slight adverse biological effects with PAH exposure in surface sediment, suggesting that PAHs are not considered as contaminants of concern in the Klang Strait. PMID:24747349

  19. Sorption of polycyclic aromatic hydrocarbons (PAHs) to lignin: effects of hydrophobicity and temperature.

    PubMed

    Zhang, Ming; Ahmad, Mahtab; Lee, Sang Soo; Xu, Li Heng; Ok, Yong Sik

    2014-07-01

    The study of the sorption of contaminants to lignin is significant for understanding the migration of contaminants in the environment as well as developing low cost sorbent. In this study, sorption of three polycyclic aromatic hydrocarbons (PAHs), naphthalene, acenaphthene and phenanthrene, to lignin was investigated. Sorption isotherms were well described by both linear and Freundlich sorption models. Sorption coefficients of PAHs to lignin from water obtained from regression of both linear model (K d) and Freundlich model (K f) were highly positively correlated with hydrophobicity of PAHs. The amorphous structure of lignin provided sufficient sorption domain for partitioning of PAHs, and the attraction between PAHs molecules and aromatic fractions in lignin via π-π electron-donor-acceptor (π-π EDA) interaction is hypothesized to provide a strong sorption force. Thermodynamic modeling revealed that sorption of PAHs to lignin was a spontaneous and exothermic process.

  20. Extraction agents for the removal of polycyclic aromatic hydrocarbons (PAHs) from soil in soil washing technologies.

    PubMed

    Lau, Ee Von; Gan, Suyin; Ng, Hoon Kiat; Poh, Phaik Eong

    2014-01-01

    Polycyclic aromatic hydrocarbons (PAHs) in soil have been recognised as a serious health and environmental issue due to their carcinogenic, mutagenic and teratogenic properties. One of the commonly employed soil remediation techniques to clean up such contamination is soil washing or solvent extraction. The main factor which governs the efficiency of this process is the solubility of PAHs in the extraction agent. Past field-scale soil washing treatments for PAH-contaminated soil have mainly employed organic solvents or water which is either toxic and costly or inefficient in removing higher molecular weight PAHs. Thus, the present article aims to provide a review and discussion of the alternative extraction agents that have been studied, including surfactants, biosurfactants, microemulsions, natural surfactants, cyclodextrins, vegetable oil and solution with solid phase particles. These extraction agents have been found to remove PAHs from soil at percentages ranging from 47 to 100% for various PAHs.

  1. Biological risk and pollution history of polycyclic aromatic hydrocarbons (PAHs) in Nansha mangrove, South China.

    PubMed

    Wu, Qihang; Leung, Jonathan Y S; Tam, Nora F Y; Chen, Shejun; Mai, Bixian; Zhou, Xizhen; Xia, Lihua; Geng, Xinhua

    2014-08-15

    Chinese government has taken various measures to alleviate pollution caused by polycyclic aromatic hydrocarbons (PAHs) in the region of Pearl River Delta since the economic reform in 1978, but the effectiveness of these measures remains largely unknown. This study aimed to elucidate the biological risk and pollution history of PAHs by measuring the concentrations of 28 PAHs in the surface and core sediments, respectively, in Nansha mangrove. Results found that the biological risk of PAHs was low without obvious spatial variation. The PAH concentration along the depth gradient indicated that PAH pollution was stabilized since the early 1990s while the source of PAHs has gradually changed from combustion of coal to petroleum products. This implied that the mitigation measures taken by the Chinese government were effective. Compared to marine bottom sediment, we propose that using mangrove sediment can provide a more accurate and precise estimate of pollution history of PAHs.

  2. A review of airborne polycyclic aromatic hydrocarbons (PAHs) and their human health effects.

    PubMed

    Kim, Ki-Hyun; Jahan, Shamin Ara; Kabir, Ehsanul; Brown, Richard J C

    2013-10-01

    Polycyclic aromatic hydrocarbons (PAHs) are a large group of organic compounds comprised of two or more fused benzene rings arranged in various configurations. PAHs are widespread environmental contaminants formed as a result of incomplete combustion of organic materials such as fossil fuels. The occurrence of PAHs in ambient air is an increasing concern because of their carcinogenicity and mutagenicity. Although emissions and allowable concentrations of PAHs in air are now regulated, the health risk posed by PAH exposure suggests a continuing need for their control through air quality management. In light of the environmental significance of PAH exposure, this review offers an overview of PAH properties, fates, transformations, human exposure, and health effects (acute and chronic) associated with their emission to the atmosphere. Biomarkers of PAH exposure and their significance are also discussed.

  3. Polycyclic aromatic hydrocarbons (PAHs) in atmospheric dustfall from the industrial corridor in Hubei Province, Central China.

    PubMed

    Zhang, Jiaquan; Qu, Chengkai; Qi, Shihua; Cao, Junji; Zhan, Changlin; Xing, Xinli; Xiao, Yulun; Zheng, Jingru; Xiao, Wensheng

    2015-10-01

    Thirty atmospheric dustfall samples collected from an industrial corridor in Hubei Province, central China, were analyzed for 16 USEPA priority polycyclic aromatic hydrocarbons (PAHs) to investigate their concentrations, spatial distributions, sources, and health risks. Total PAH concentrations (ΣPAHs) ranged from 1.72 to 13.17 µg/g and averaged 4.91 µg/g. High molecular weight (4-5 rings) PAHs averaged 59.67% of the ΣPAHs. Individual PAH concentrations were not significantly correlated with total organic carbon, possibly due to the semi-continuous inputs from anthropogenic sources. Source identification studies suggest that the PAHs were mainly from motor vehicles and biomass/coal combustion. The incremental lifetime cancer risks associated with exposure to PAHs in the dustfall ranged from 10(-4) to 10(-6); these indicate potentially serious carcinogenic risks for exposed populations in the industrial corridor.

  4. Toxicity assessment of polycyclic aromatic hydrocarbons in sediments from European high mountain lakes.

    PubMed

    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.

  5. Identification of polycyclic aromatic hydrocarbons in unleaded petrol and diesel exhaust emission.

    PubMed

    Yadav, Vinay Kumar; Prasad, Sahdeo; Patel, Devendra K; Khan, Altaf Husain; Tripathi, Madhu; Shukla, Yogeshwer

    2010-09-01

    Inhalation of emissions from petrol and diesel exhaust particulates is associated with potentially severe biological effects. In the present study, polycyclic aromatic hydrocarbons (PAHs) were identified from smokes released by the automobile exhaust from petrol and diesel. Intensive sampling of unleaded petrol and diesel exhaust were done by using 800-cm(3) motor car and 3,455-cm(3) vehicle, respectively. The particulate phase of exhaust was collected on Whatman filter paper. Particulate matters were extracted from filter paper by using Soxhlet. PAHs were identified from particulate matter by reverse phase high performance liquid chromatography using C(18) column. A total of 14 PAHs were identified in petrol and 13 in case of diesel sample after comparing to standard samples for PAH estimation. These inhalable PAHs released from diesel and petrol exhaust are known to possess mutagenic and carcinogenic activity, which may present a potential risk for the health of inhabitants.

  6. [Contamination and source of polycyclic aromatic hydrocarbons in epikarst spring water].

    PubMed

    Sun, Yu-Chuan; Shen, Li-Cheng; Yuan, Dao-Xian

    2014-06-01

    The water samples were collected from four typical epikarst springs in Nanchuan District, Chongqing Municipality between October 2010 and October 2011. Sixteen priority polycyclic aromatic hydrocarbons in epikarst spring waters were quantitatively analyzed by the gas chromatography-mass spectrometer (GC-MS). The objectives of this study were to investigate the seasonal variations of polycyclic aromatic hydrocarbons' concentration, composition, source and contamination characterization in epikarst springs water. The results showed that the detection ratios of 16 PAHs in four springs were 100%. The total concentrations of 16 PAHs fluctuated greatly in epikarst spring water during one year observation, and the concentration ranged from 341 to 4 968 ng x L(-1), with a mean value of 1772 ng x L(-1). The total concentrations of 7 carcinogenic PAHs in rain season were all higher than those in dry season in four epikarst springs. The PAHs profiles were dominated by (2-3) rings PAHs in spring water, which accounted for more than 50% of 16 PAHs. The PAHs in spring water mainly originated from the combustion of coal, biomass and petroleum, and during June to October 2011, PAHs originated from the combustion of coal and biomass had a larger contribution. The ratios of Ant/( Ant + Phe) and Fla/( Fla + Pyr) changing with seasons showed that Ant, Phe, Fla and Pyr were easy to migrate in epikarst soils. In 4 isomeric ratios, the ratios of Fla/(Fla + Pyr) were more sensitive to reflect the information of sources. Compared to other areas in the world, the concentration of 16 PAHs in epikarst spring water is at a higher level, which shows the epikarst spring water has been suffered the PAHs pollution.

  7. Theoretical Infrared Spectra for Polycyclic Aromatic Hydrocarbon Neutrals, Cations and Anions

    NASA Technical Reports Server (NTRS)

    Langhoff, Stephen R.

    1995-01-01

    Calculations are carried out using density functional theory (DFT) to determine the harmonic frequencies and intensities of the neutrals and cations of thirteen polycyclic aromatic hydrocarbons (PAHs) up to the size of ovalene. Calculations are also carried out for a few PAH anions. The DFT harmonic frequencies, when uniformly scaled by the factor of 0.958 to account primarily for anharmonicity, agree with the matrix isolation fundamentals to within an average error of about 10 per centimeter. Electron correlation is found to significantly reduce the intensities of many of the cation harmonics, bringing them into much better agreement with the available experimental data. While the theoretical infrared spectra agree well with the experimental data for the neutral systems and for many of the cations, there are notable discrepancies with the experimental matrix isolation data for some PAH cations that are difficult to explain in terms of limitations in the calculations. In agreement with previous theoretical work, the present calculations show that the relative intensities for the astronomical unidentified infrared (UIR) bands agree reasonably well with those for a distribution of polycyclic aromatic hydrocarbon (PAH) cations, but not with a distribution of PAH neutrals. We also observe that the infrared spectra of highly symmetrical cations such as coronene agree much better with astronomical observations than do those of, for example, the polyacenes such as tetracene and pentacene. The total integrated intensities for the neutral species are found to increase linearly with size, while the total integrated intensities are much larger for the cations and scale more nearly quadratically with size. We conclude that emission from moderate-sized highly symmetric PAH cations such as coronene and larger could account for the UIR bands.

  8. Urinary metabolites of polycyclic aromatic hydrocarbons in Saudi Arabian schoolchildren in relation to sources of exposure.

    PubMed

    Alghamdi, Mansour A; Alam, Mohammed S; Stark, Christopher; Mohammed, Nuredin; Harrison, Roy M; Shamy, Magdy; Khoder, Mamdouh I; Shabbaj, Ibrahim I; Göen, Thomas

    2015-07-01

    Polycyclic aromatic hydrocarbons contain a number of known carcinogenic compounds, and urinary biomarkers have been widely used as a measure of exposure but quantitative relationships with exposure variables have proved elusive. This study aimed to quantify the relationship between exposures to phenanthrene and pyrene from atmospheric and dietary sources with the excretion of 1-hydroxypyrene and hydroxyphenanthrenes in urine as biomarkers of exposure. The study population consisted of 204 male schoolchildren attending three schools in different parts of Jeddah, Saudi Arabia who provided urine samples on each of three consecutive days. Outdoor air measurements of polycyclic aromatic hydrocarbons were made at the schools and the children provided information on diet, exposure to environmental tobacco smoke and incense, and various lifestyle factors through a questionnaire. Mixed models with random effects for subjects nested within site were fitted in order to examine the relationship between exposure variables and urinary PAH metabolites. A unit increase (1 ng m(-3)) in ambient pyrene (particulate plus gaseous phase) was associated with a 3.5% (95% CI: 1.01%, 5.13%) increase in urinary 1-hydroxypyrene concentration. A unit increase in ambient phenanthrene was associated with a 1.01% (95% CI: 0.03%, 2.02%) increase in total hydroxyphenanthrene concentrations. Consumption of chargrilled food increased the 1-hydroxypyrene and hydroxyphenanthrene concentrations by 24% (95% CI: 11%, 37%) and 17% (95% CI: 8%, 26%) respectively. We did not find evidence of association for environmental tobacco smoke exposure or incense burning. It is concluded that both respiratory exposure and consumption of chargrilled food are considerable sources of PAH exposure in this population as reflected by concentrations of urinary biomarkers.

  9. [Improving Agricultural Safety of Soils Contaminated with Polycyclic Aromatic Hydrocarbons by In Situ Bioremediation].

    PubMed

    Jiao, Hai-huan; Pan, Jian-gang; Xu, Shena-jun; Bai, Zhi-hui; Wang, Dong; Huang, Zhan-bin

    2015-08-01

    In order to reduce the risk of enrichment of polycyclic aromatic hydrocarbons (PAHs) in crops, reduce the potential hazards of food-sourced PAHs to human and increase the agricultural safety of PAHs contaminated soils, the bio-augmented removal of polycyclic aromatic hydrocarbons (PAHs) was investigated through in situ remediation by introducing Rhodobacter sphaeroides (RS) into the agricultural soil contaminated by PAHs. The 50-times diluted RS was sprayed on leaf surface (in area B) or irrigated to roots (in area D). The treatment of spraying water of the equal amount was taken as the control (A) and the wheat field without any treatment as the blank (CK). Treatments were conducted since wheat seeding. Soil and wheat samples were collected in the mature period to analyze the changes of community structure of the soil microorganisms and the concentration of PAHs in soils and investigate the strengthening and restoration effects of RS on PAHs contaminated soils. Compared to the CK Area, the areas B and D revealed that the variation ratio of phospholipid fatty acids (PLFAs) that were the biomarker of soil microorganisms was 29.6%, and the ratio of total PAHs removed was increased 1.59 times and 1.68 times, respectively. The dry weight of wheat grain of 50 spikes was increased by 8.95% and 12.5%, respectively, and the enrichment factor of total PAHs was decreased by 58.9% and 62.2% respectively in the wheat grains. All the results suggested that RS reduced enrichment of PAHs in wheat grains and increased wheat yield, which had great exploitation and utilization potentiality in repairing and improving the agricultural safety of the soils contaminated with PHAs.

  10. Microbial degradation of polycyclic aromatic hydrocarbon and cyanide in soils from manufactured gas plant sites

    SciTech Connect

    Ho, YiFong.

    1993-01-01

    The microbial clean-up of cyanide and polycyclic aromatic hydrocarbon (PAH) in soils from manufactured gas plant (MGP) sites is the subject of this study. Cyanide was examined for its inhibition on microbial PAH degradation by an MGP-soil isolate identified as a strain of Pseudomonas aeruginosa by classical differential methods as well as 16S rRNA oligonucleotide probes. A strong cyanide-degrading Bacillus pumilus (ATCC No. 7061) strain was used for facilitating cyanide degradation thereby enhancing PAH biodegradation in this soil. This research has validated cyanide interference with the PAH degrader and shown that adding Bacillus pumilus accomplishes the removal of cyanide which subsequently allows Pseudomonas aeruginosa to metabolize PAHs. In addition to the biodegradation of cyanide and lower ring numbered PAHs, the microbial degradation of 4-ring polycyclic aromatic hydrocarbons (PAHs) by using a mixed culture obtained from another former coal tar contaminated site was also studied. The rate of biotransformation and the abiotic loss due to volatilization were monitored. The 3-ring PAH used in this project was phenanthrene and the 4-ring PAHs used were fluoranthene and pyrene. The results showed that volatilization loss of naphthalene in the control system was substantial while volatilization of higher molecular weight PAH compounds (fluoranthene and pyrene) was negligible. The biodegradation rates of phenanthrene, fluoranthene and pyrene are 6.56, 1.59 and 0.82 mg/L/day, respectively or 65.6, 15.9, 8.2 mg/gram of cells/day assuming 100 mg cells/L in the system. This study indicates that biodegradation of 3- and 4-ring PAHs by mixed cultures obtained from PAH contaminated sites is very promising. These studies will contribute to the understanding of PAH and cyanide removal from MGP and provide information for the design of a bioremediation project to reclaim unusable land that was contaminated through the previous coal gasification process.

  11. Laboratory investigation of the contribution of complex aromatic/aliphatic polycyclic hybrid molecular structures to interstellar ultraviolet extinction and infrared emission

    NASA Technical Reports Server (NTRS)

    Arnoult, K. M.; Wdowiak, T. J.; Beegle, L. W.

    2000-01-01

    We have demonstrated by experiment that, in an energetic environment, a simple polycyclic aromatic hydrocarbon (PAH) such as naphthalene will undergo chemical reactions that produce a wide array of more complex species (an aggregate). For a stellar wind of a highly evolved star (post-asymptotic giant branch [post-AGB]), this process would be in addition to what is expected from reactions occurring under thermodynamic equilibrium. A surprising result of that work was that produced in substantial abundance are hydrogenated forms that are hybrids of polycyclic aromatic and polycyclic alkanes. Infrared spectroscopy described here reveals a spectral character for these materials that has much in common with that observed for the constituents of circumstellar clouds of post-AGB stars. It can be demonstrated that a methylene (-CH2-) substructure, as in cycloalkanes, is the likely carrier of the 6.9 microns band emission of dust that has recently been formed around IRAS 22272+5433, NGC 7027, and CPD -56 8032. Ultraviolet spectroscopy previously done with a lower limit of 190 nm had revealed that this molecular aggregate can contribute to the interstellar extinction feature at 2175 angstroms. We have now extended our UV spectroscopy of these materials to 110 nm by a vacuum ultraviolet technique. That work, described here, reveals new spectral characteristics and describes how material newly formed during the late stages of stellar evolution could have produced an extinction feature claimed to exist at 1700 angstroms in the spectrum of HD 145502 and also how the newly formed hydrocarbon material would be transformed/aged in the general interstellar environment. The contribution of this molecular aggregate to the rise in interstellar extinction at wavelengths below 1500 angstroms is also examined. The panspectral measurements of the materials produced in the laboratory, using plasmas of H, He, N, and O to convert the simple PAH naphthalene to an aggregate of complex species

  12. Supra-Atomic Coarse-Grained GROMOS Force Field for Aliphatic Hydrocarbons in the Liquid Phase.

    PubMed

    Eichenberger, Andreas P; Huang, Wei; Riniker, Sereina; van Gunsteren, Wilfred F

    2015-07-14

    A supra-atomic coarse-grained (CG) force field for liquid n-alkanes is presented. The model was calibrated using experimental thermodynamic data and structural as well as energetic properties for 14 n-alkanes as obtained from atomistic fine-grained (FG) simulations of the corresponding hydrocarbons using the GROMOS 45A3 biomolecular force field. A variation of the nonbonded force-field parameters obtained from mapping the FG interactions onto the CG degrees of freedom to fit the density and heat of vaporization to experimental values turned out to be mandatory for a correct reproduction of these data by the CG model, while the bonded force-field parameters for the CG model could be obtained from a Boltzmann-weighted fit with some variations with respect to the corresponding properties from the FG simulations mapped onto the CG degrees of freedom. The model presents 6 different CG bead types, for bead sizes from 2 to 4 distinguishing between terminal and nonterminal beads within an alkane chain (end or middle). It contains different nonbonded Lennard-Jones parameters for the interaction of CG alkanes with CG water. The CG alkane model was further tested by comparing predictions of the excess free energy, the self-diffusion constant, surface tension, isothermal compressibility, heat capacity, thermal expansion coefficient, and shear viscosity for n-alkanes to experimental values. The CG model offers a thermodynamically calibrated basis for the development of CG models of lipids.

  13. Isolation and characterization of a Mycobacterium species capable of degrading three- and four-ring aromatic and aliphatic hydrocarbons

    SciTech Connect

    Churchill, S.A.; Harper, J.P.; Churchill, P.F.

    1999-02-01

    Mycobacterium sp. strain CH1 was isolated from polycyclic aromatic hydrocarbon (PAH)-contaminated freshwater sediments and identified by analysis of 16S rDNA sequences. Strain CH1 was capable of mineralizing three- and four-ring PAHs including phenanthrene, pyrene, and fluoranthene. In addition, strain CH1 could utilize phenanthrene or pyrene as a sole carbon and energy source. A lag phase of at least 3 days was observed during pyrene mineralization. This lag phase decreased to less than 1 day when strain CH1 was grown in the presence of phenanthrene or fluoranthene. Strain CH1 also was capable of using a wide range of alkanes as sole carbon and energy sources. No DNA hybridization was detected with the nahAc gene probe, indicating that enzymes involved in PAH metabolism are not related to the well-characterized naphthalene dioxygenase gene. DNA hybridization was not detected when the alkB gene from Pseudomonas oleovorans was used under high-stringency conditions. However, there was slight but detectable hybridization under low-stringency conditions. This suggests a distant relationship between genes involved in alkane oxidation.

  14. Atmospheric pressure gas chromatography with quadrupole time of flight mass spectrometry for simultaneous detection and quantification of polycyclic aromatic hydrocarbons and nitro-polycyclic aromatic hydrocarbons in mosses.

    PubMed

    Domeño, Celia; Canellas, Elena; Alfaro, Pilar; Rodriguez-Lafuente, Angel; Nerin, Cristina

    2012-08-24

    Within the family of polycyclic aromatic hydrocarbons (PAHs), nitrated derivatives are of particular interest in environmental science because they have well-known carcinogenic and mutagenic effects. They are in fact more toxic than their parent PAHs. One valuable diagnosis of atmospheric pollution can be obtained using biomonitors such as mosses. These biomonitors can provide information about air pollution over long periods of time in wilderness areas. Thus, they can serve as monitors of the atmospheric transport of pollutants. In this study, atmospheric pressure gas chromatography coupled to a quadrupole hyphenated to a time of flight mass spectrometer (APGC-MS/Q-TOF) has been examined for the identification of target analytes (15 PAHs and 8 NPAHs) for subsequent use in the analysis of mosses. Working ranges in low μg g(-1) concentration levels were obtained with most correlation coefficients higher than 0.999. All LODs were in the 0.007-0.035μg g(-1) range and higher LODs (0.035μg g(-1)) were obtained for the less volatile PAHs with higher mass and retention times: benzo(g,h,i)perylene, dibenz(a,h)anthracene and indeno(1,2,3-c,d)pyrene. These LODs are of importance for the intended use, biomonitoring, especially taking into account that NPAHs are commonly found at very low concentration levels. Recoveries from mosses ranged from 75 to 98%. Intraday and interday precision ranged from 1.8 to 11.1% RSD and from 2.4 to 16.7% RSD, respectively. Very low concentrations of NPAHs were found in mosses compared to those of PAHs. All these data were used for pattern recognition of the pollutant source. The results are shown and discussed.

  15. Polytetrafluoroethylene-jacketed stirrer modified with graphene oxide and polydopamine for the efficient extraction of polycyclic aromatic hydrocarbons.

    PubMed

    Zhang, Zinxin; Mwadini, Mwadini Ahmada; Chen, Zilin

    2016-10-01

    Steel stirrers jacketed with polytetrafluoroethylene can be regarded as an ideal substrate for stirrer bar sorptive extraction. However, it is still a great challenge to immobilize graphene onto a polytetrafluoroethylene stirrer due to the high chemical resistance of the surface of a polytetrafluoroethylene stirrer. We describe here a method to modify the surface of polytetrafluoroethylene stirrers with graphene. In this work, graphene was used as the sorbent due to its excellent adsorption capability for aromatic compounds, such as polycyclic aromatic compounds. Graphene was successfully immobilized onto polytetrafluoroethylene-stirrer by a bio-inspired polydopamine functionalization method. The graphene-modified polytetrafluoroethylene-stirrer shows good stability and tolerance to stirring, ultrasonication, strong acidic and basic solutions, and to organic solvents. The multilayer coating was characterized by scanning electronic microscopy and Fourier transform infrared spectroscopy. After the optimization of some experimental conditions, the graphene-modified polytetrafluoroethylene stirrer was used for the stirrer bar sorptive extraction of polycyclic aromatic hydrocarbons, in which the binding between the polycyclic aromatic hydrocarbons and the graphene layer was mainly based on π-π stacking and hydrophobic interactions. The graphene-modified polytetrafluoroethylene-stirrer-based stirrer bar sorptive extraction and high-performance liquid chromatography method was developed for the determination of polycyclic aromatic hydrocarbons with great extraction efficiency, with enrichment factors from 18 to 62. The method has low limits of detection of 1-5 pg/mL, wide linear range (5-100 and 10-200 pg/mL), good linearity (R ≥ 0.9957) and good reproducibility (RSD ≤ 6.45%). The proposed method has been applied to determine polycyclic aromatic hydrocarbons in real dust samples. Good recoveries were obtained, ranging from 88.53 to 109.43%.

  16. The bioflavonoid galangin blocks aryl hydrocarbon receptor activation and polycyclic aromatic hydrocarbon-induced pre-B cell apoptosis.

    PubMed

    Quadri, S A; Qadri, A N; Hahn, M E; Mann, K K; Sherr, D H

    2000-09-01

    Bioflavonoids are plant compounds touted for their potential to treat or prevent several diseases including cancers induced by common environmental chemicals. Much of the biologic activity of one such class of pollutants, polycyclic aromatic hydrocarbons (PAH), is mediated by the aryl hydrocarbon receptor/transcription factor (AhR). For example, the AhR regulates PAH immunotoxicity that manifests as pre-B cell apoptosis in models of B cell development. Because bioflavonoids block PAH-induced cell transformation and are structurally similar to AhR ligands, it was postulated that some of them would suppress PAH-induced, AhR-dependent immunotoxicity, possibly through a direct AhR blockade. This hypothesis was tested using a model of B cell development in which pre-B cells are cultured with and are dependent on bone marrow stromal or hepatic parenchymal cell monolayers. Of seven bioflavonoids screened, galangin (3,5,7-trihydroxyflavone) blocked PAH-induced but not C(2)-ceramide- or H(2)O(2)-induced pre-B cell apoptosis. Because galangin blocked AhR-dependent reporter gene expression, AhR complex-DNA binding, and AhR nuclear translocation, inhibition of a relatively early step in AhR signaling was implicated. This hypothesis was supported by the ability of galangin to bind the AhR and stabilize AhR-90-kDa heat shock protein complexes in the presence of AhR agonists. These studies demonstrate the utility of pre-B cell culture systems in identifying compounds capable of blocking PAH immunotoxicity, define at least one mechanism of galangin activity (i.e., repression of AhR activation), and motivate the use of this and similar dietary bioflavonoids as relatively nontoxic inhibitors of AhR agonist activity and as pharmacologic agents with which to dissect AhR signaling pathways.

  17. Identification of benzothiazole derivatives and polycyclic aromatic hydrocarbons as aryl hydrocarbon receptor agonists present in tire extracts.

    PubMed

    He, Guochun; Zhao, Bin; Denison, Michael S

    2011-08-01

    Leachate from rubber tire material contains a complex mixture of chemicals previously shown to produce toxic and biological effects in aquatic organisms. The ability of these leachates to induce Ah receptor (AhR)-dependent cytochrome P4501A1 expression in fish indicated the presence of AhR active chemicals, but the responsible chemicals and their direct interaction with the AhR signaling pathway were not examined. Using a combination of AhR-based bioassays, we have demonstrated the ability of tire extract to stimulate both AhR DNA binding and AhR-dependent gene expression and confirmed that the responsible chemicals were metabolically labile. The application of CALUX (chemical-activated luciferase gene expression) cell bioassay-driven toxicant identification evaluation not only revealed that tire extract contained a variety of known AhR-active polycyclic aromatic hydrocarbons but also identified 2-methylthiobenzothiazole and 2-mercaptobenzothiazole as AhR agonists. Analysis of a structurally diverse series of benzothiazoles identified many that could directly stimulate AhR DNA binding and transiently activate the AhR signaling pathway and identified benzothiazoles as a new class of AhR agonists. In addition to these compounds, the relatively high AhR agonist activity of a large number of fractions strongly suggests that tire extract contains a large number of physiochemically diverse AhR agonists whose identities and toxicological/biological significances are unknown.

  18. Identification of Benzothiazole Derivatives and Polycyclic Aromatic Hydrocarbons as Aryl Hydrocarbon Receptor Agonists Present in Tire Extracts

    PubMed Central

    He, Guochun; Zhao, Bin; Denison, Michael S.

    2012-01-01

    Leachate from rubber tire material contains a complex mixture of chemicals previously shown to produce toxic and biological effects in aquatic organisms. While the ability of these leachates to induce Ah receptor (AhR)-dependent cytochrome P4501A1 expression in fish indicated the presence of AhR active chemicals, the responsible chemical(s) and their direct interaction with the AhR signaling pathway were not examined. Using a combination of AhR-based bioassays, we have demonstrated the ability of tire extract to stimulate both AhR DNA binding and AhR-dependent gene expression and confirmed that the responsible chemical(s) was metabolically labile. The application of CALUX (Chemical-Activated LUciferase gene eXpression) cell bioassay-driven toxicant identification evaluation not only revealed that tire extract contained a variety of known AhR-active polycyclic aromatic hydrocarbons, but also identified 2-methylthiobenzothiazole and 2-mercaptobenzothiazole as AhR agonists. Analysis of a structurally diverse series of benzothiazoles identified many that could directly stimulate AhR DNA binding and transiently activate the AhR signaling pathway and identified benzothiazoles as a new class of AhR agonists. In addition to these compounds, the relatively high AhR agonist activity of a large number of fractions strongly suggests that tire extract contains a large number of physiochemically diverse AhR agonists whose identities and toxicological/biological significances are unknown. PMID:21590714

  19. Ex-situ bioremediation of polycyclic aromatic hydrocarbons in sewage sludge.

    PubMed

    Larsen, Sille Bendix; Karakashev, Dimitar; Angelidaki, Irini; Schmidt, Jens Ejbye

    2009-05-30

    Polycyclic aromatic hydrocarbons (PAH) are regarded as environmental pollutants. A promising approach to reduce PAH pollution is based on the implementation of the natural potential of some microorganisms to utilize hydrocarbons. In this study Proteiniphilum acetatigenes was used for bioaugmentation of sewage sludge to improve the PAH removal. Bioaugmentation experiments were performed in parallel semi-continuously fed reactors started up with digested primary and secondary sludge. Three bioaugmentation approaches were investigated: A1, addition of bacteria once during starting up; A2, addition of bacteria at the beginning and then every 2nd day and A3, addition of encapsulated bacteria once during starting up. Removal of PAH was found to be both biotic and abiotic. All three approaches had a positive effect of the biological removal of PAH. Highest biological removal of individual PAH (up to 80%) was observed using continuous addition (approach A2) of the bacteria to the reactors. In general, the effect of bioaugmentation was higher in the reactors fed with primary sludge compared to the reactors fed with mixed sludge. Bioaugmentation resulted in biological removal of low molecular weight PAH in the reactors fed with primary sludge using all three approaches while clear biological removal of the medium- and high molecular weight PAH only was observed if the bacteria were added continuously (approach A2).

  20. Assessing the Ecological Risk of Polycyclic Aromatic Hydrocarbons in Sediments at Langkawi Island, Malaysia

    PubMed Central

    Nasher, Essam; Heng, Lee Yook; Zakaria, Zuriati; Surif, Salmijah

    2013-01-01

    Tourism-related activities such as the heavy use of boats for transportation are a significant source of petroleum hydrocarbons that may harm the ecosystem of Langkawi Island. The contamination and toxicity levels of polycyclic aromatic hydrocarbon (PAH) in the sediments of Langkawi were evaluated using sediment quality guidelines (SQGs) and toxic equivalent factors. Ten samples were collected from jetties and fish farms around the island in December 2010. A gas chromatography/flame ionization detector (GC/FID) was used to analyse the 18 PAHs. The concentration of total PAHs was found to range from 869 ± 00 to 1637 ± 20 ng g−1 with a mean concentration of 1167.00 ± 24 ng g−1, lower than the SQG effects range-low (3442 ng g−1). The results indicated that PAHs may not cause acute biological damage. Diagnostic ratios and principal component analysis suggested that the PAHs were likely to originate from pyrogenic and petrogenic sources. The toxic equivalent concentrations of the PAHs ranged from 76.3 to 177 ng TEQ/g d.w., which is lower compared to similar studies. The results of mean effects range-median quotient of the PAHs were lower than 0.1, which indicate an 11% probability of toxicity effect. Hence, the sampling sites were determined to be the low-priority sites. PMID:24163633