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Sample records for 4-6 ring pahs

  1. PAH and H2 emission in the Ring Nebula

    NASA Astrophysics Data System (ADS)

    Cox, N. L. J.; Pilleri, P.; Berné, O.; Cernicharo, J.; Joblin, C.

    2016-07-01

    This paper presents the Spitzer IRS (Infra Red Spectrograph) detection of mid-infrared polycyclic aromatic hydrocarbon (PAH) emission features and H2 associated with dense knots in the ring of the “oxygen-rich” (C/O∼⃒0.6-0.8) planetary nebula (PN) NGC6720 (Ring Nebula). We explored a further three oxygen-rich extended PNe with similar dataset available. These turned out to be non-detection of PAHs, although two of these do contain H2 emission knots. The presence of PAHs is discussed in the context of a bottom-up formation mechanism, in which first small hydrocarbons, and later PAHs, are formed in warm dense knots inside the ionised regions of PNe.

  2. Buckling tests of two 4.6-meter-diameter, magnesium ring-stiffened conical shells loaded under external pressure

    NASA Technical Reports Server (NTRS)

    Anderson, J. K.; DAVIS R. C.

    1973-01-01

    Two ring-stiffened magnesium conical shells with a 120 deg apex angle and a 4.6-meter diameter were loaded to failure by a uniform external pressure. The cones differed from one another only in the number of internal stiffening rings. Test specimen details, test procedure, and test results are discussed. Both buckling and prebuckling data are compared with appropriate theoretical predictions. Measured strains in skin and rings agreed well with theoretical predictions. Extensive imperfection measurements were made and reported on both cones in the as fabricated condition.

  3. SYNTHESIS AND BIOLOGICAL ACTIVITY OF CYCLOPENTA EPOXIDES OF PAH (POLYCYCLIC AROMATIC HYDROCARBONS) CONTAINING PERIPHERALLY FUSED CYCLOPENTA RINGS

    EPA Science Inventory

    Polycyclic aromatic hydrocarbons (PAH) containing peripherally fused cyclopenta rings have been identified in soots from many different combustion sources. Metabolism and mutagenicity studies have been reported on the series of four cyclopenta-fused isomers derived from benzanthr...

  4. Effects of polycyclic aromatic hydrocarbons on microbial community structure and PAH ring hydroxylating dioxygenase gene abundance in soil.

    PubMed

    Sawulski, Przemyslaw; Clipson, Nicholas; Doyle, Evelyn

    2014-11-01

    Development of successful bioremediation strategies for environments contaminated with recalcitrant pollutants requires in-depth knowledge of the microorganisms and microbial processes involved in degradation. The response of soil microbial communities to three polycyclic aromatic hydrocarbons, phenanthrene (3-ring), fluoranthene (4-ring) and benzo(a)pyrene (5-ring), was examined. Profiles of bacterial, archaeal and fungal communities were generated using molecular fingerprinting techniques (TRFLP, ARISA) and multivariate statistical tools were employed to interpret the effect of PAHs on community dynamics and composition. The extent and rate of PAH removal was directly related to the chemical structure, with the 5-ring PAH benzo(a)pyrene degraded more slowly than phenathrene or fluoranthene. Bacterial, archaeal and fungal communities were all significantly affected by PAH amendment, time and their interaction. Based on analysis of clone libraries, Actinobacteria appeared to dominate in fluoranthene amended soil, although they also represented a significant portion of the diversity in phenanthrene amended and unamended soils. In addition there appeared to be more γ-Proteobacteria and less Bacteroidetes in soil amended with either PAH compared to the control. The soil bacterial community clearly possessed the potential to degrade PAHs as evidenced by the abundance of PAH ring hydroxylating (PAH-RHDα) genes from both gram negative (GN) and gram positive (GP) bacteria in PAH-amended and control soils. Although the dioxygenase gene from GP bacteria was less abundant in soil than the gene associated with GN bacteria, significant (p < 0.001) increases in the abundance of the GP PAH-RHDα gene were observed during phenanthrene and fluoranthene degradation, whereas there was no significant difference in the abundance of the GN PAH-RHDα gene during the course of the experiment. Few studies to-date have examined the effect of pollutants on more than one microbial

  5. 2-pyrazinylnitrene and 4-pyrimidylnitrene. Ring expansion to 1,3,5-triazacyclohepta-1,2,4,6-tetraene and ring opening to (2-Isocyanovinyl)carbodiimide.

    PubMed

    Addicott, Chris; Wong, Ming Wah; Wentrup, Curt

    2002-11-29

    Tetrazolo[1,5-a]pyrazine/2-azidopyrazine 9T/9A undergo photolysis in Ar matrix at cryogenic temperatures to yield 1,3,5-triazacyclohepta-1,2,4,6-tetraene 21 as the first observable intermediate, and 1-cyanoimidazole 11 and (2-isocyanovinyl)carbodiimide 22 as the final products. The latter tautomerizes to 2-(isocyanovinyl)cyanamide 23 on warming to 40 K. The same intermediate 21 and the same final products are obtained on matrix photolysis of the isomeric tetrazolo[1,5-c]pyrimidine/4-azidopyrimidine 24T/24A. These photolysis results as well as those of the previously reported thermal ring contraction of (15)N-labeled 2-pyrazinyl- and 4-pyrimidylnitrenes to 1-cyanoimidazoles can all be rationalized in terms of selective ring opening of 21 or nitrine 10 to a nitrile ylide zwitterion 28 prior to formation of the final products, 11 and 22. The results are supported by high-level ab initio and DFT calculations (CASPT2-CASSCF(6,6), G3(MP2), and B3LYP/6-31+G) of the energies and IR spectra of the intermediates and products. PMID:12444636

  6. Biomonitoring airborne parent and alkylated three-ring PAHs in the Greater Cologne Conurbation II: regional distribution patterns.

    PubMed

    Lehndorff, E; Schwark, L

    2009-05-01

    The spatial distribution of an important air pollutant class, three-ring polycyclic aromatic hydrocarbons and their derivatives (PAH-3), has been monitored for the Greater Cologne Conurbation (GCC) using pine needle as passive samplers. The GCC comprises one of the most heavily populated, trafficked, and industrialized regions in Germany. Here, 71 locations covering 3600 km(2) were sampled and, for the first time, isopleths maps constructed to investigate the regional variability in PAH-3 concentration and composition. The highest PAH-3 loads on needles (1000-1500 ng g(-1)) were detected downwind of three lignite fuelled power plants, followed by Cologne City (600-700 ng g(-1)) and smaller towns (400-600 ng g(-1)), whereas rural and forest regions yielded PAH-3 loads of 60-300 ng g(-1). PAH-3 ratios facilitated source reconciliation, with high dibenzothiophene versus retene values indicating lignite combustion and high 9/(9+1)-methylphenanthrene ratios depicting traffic emissions in inner cities. PAH-3 ratios depended on topography and outlined the heavily industrialized Rhine Valley, demonstrating atmospheric dispersal of PAH-3. PMID:19157662

  7. The Coagulant Type Influence on Removal Efficiency of 5- and 6-Ring Pahs During Water Coagulation Process

    NASA Astrophysics Data System (ADS)

    Nowacka, Anna; Włodarczyk-Makuła, Maria

    2014-12-01

    The article presents results on investigation of the removal efficiency of selected 5- and 6-ring polycyclic aromatic hydrocarbons (benzo[a]pyrene, benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[j]fluoranthene, benzo[g,h,i]perylene, indeno[1,2,3-cd]pyrene, dibenzo[a,h]anthracene) from water during coagulation and sedimentation process. Two pre-hydrolyzed aluminum coagulants: PAX XL 19H and FLOKOR 105V were chosen for research. Process was carried out at optimum process parameters: rapid-mixing - 3 min at the rotational speed of 200 rpm, slow mixing - 10 min at 30 rpm, sedimentation - 60 min. The removal effectiveness was dependant on coagulant type and its composition. Better results in the removal of 5-and 6-ring PAHs were obtained after application of FLOKOR 105V (lower aluminum content) than after using PAX XL 19H.

  8. Synthesis and cytotoxic activities of 2-substituted (25R)-spirostan-1,4,6-triene-3-ones via ring-opening/elimination and 'click' strategy.

    PubMed

    Lu, Xiao-Feng; Yang, Zheng; Huang, Nian-Yu; He, Hai-Bo; Deng, Wei-Qiao; Zou, Kun

    2015-09-01

    To develop more effective antitumor steroidal drugs, we synthesized a library including twenty-two novel cytotoxic 2-alkyloxyl substituted (25R)-spirostan-1,4,6-triene-3-ones and corresponding 1,2,3-triazoles through an abnormal monoepoxide ring-opening/elimination and 'click' reactions. After the cytotoxic evaluations against HepG2, Caski and HeLa cell lines, three steroidal triazoles 5b, 5f and 5m in this library were found to possess potent anti-proliferative effects against Caski cells with the half-inhibitory concentrations (IC50) of 9.4-11.8 μM. The high-efficient and straightforward process was attractive feature for facile preparation of anti-tumor steroidal triazoles. PMID:26141770

  9. Pulsed Discharge Nozzle Cavity Ring Down Spectroscopy of Cold PAH Ions

    NASA Technical Reports Server (NTRS)

    Biennier, Ludovic; Salama, Farid; Allamandola, Louis J.; Scherer, James J.; DeVincenzi, Donald (Technical Monitor)

    2002-01-01

    The gas-phase electronic absorption spectra of the naphthalene (C10H8(+)) and acenaphthene (C12H10(+)) cations have been measured in the visible range in a free 10 jet planar expansion in an attempt to collect data in an astrophysically relevant environment. The direct absorption spectra of two out of four bands measured of the gas-phase cold naphthalene cation along with the gas-phase vibronic absorption spectrum of the cold acenaphthene cation are reported for the first time. The study has been carried out using the ultrasensitive and versatile technique of cavity ringdown spectroscopy (CRDS) coupled to a pulsed discharge slit nozzle (PDN). The new CRDS-PDN set up is described and its characteristics are evaluated. The direct-absorption spectra of the PAH ions are discussed and compared to the gas-phase and solid-phase data available in the literature. The analysis of the results show that cold, free flying PAH ions are generated in the argon discharge primarily through soft Penning ionization. This enables the intrinsic band profiles to be measured, a key requirement for astrophysical applications.

  10. Distribution and accumulation of polycyclic aromatic hydrocarbons (PAHs) in the food web of Nansi Lake, China.

    PubMed

    Zhang, Guizhai; Pan, Zhaoke; Wang, Xiaoming; Mo, Xiaojie; Li, Xiaoming

    2015-04-01

    The concentrations of polycyclic aromatic hydrocarbons (PAHs) were analyzed in water, sediment, and biota (aquatic plant, shrimp, and fish) of Nansi Lake by gas chromatography-mass spectrometry (GC-MS). The concentrations of total PAHs were 27.54-55.04 ng L(-1) in water, 80.31-639.23 ng g(-1) dry weight (dw) in sediments, 20.92-192.78 ng g(-1) dw in aquatic plants, and 67.3-533.9 ng g(-1) dw in fish and shrimp muscles. The ratios of phenanthrene to anthracene (Ph/An), fluoranthene to pyrene (Flu/Pyr), and low molecular weight to high molecular weight (LMW/HMW) in sediment indicated that the sources of the PAHs were a mixture of pyrolytic and petrogenic contamination at most sampling sites in Nansi Lake. The composition profile of PAHs in plants was similar to that in water and animals with 2-3 ring PAHs being dominant. The 4-6 ring PAHs were the dominant PAH compounds in sediment. There is a positive correlation between sediment and aquatic plants, but their PAH composition profiles were different, implying that aquatic plant absorption of PAHs from sediment is selective and the accumulation of PAHs in aquatic plants is different. The concentration of PAHs in fish showed a positive correlation with plants, reflecting that the PAHs in fish are mainly absorbed from aquatic plants rather than directly from the water. Bioaccumulation of LMW PAHs in aquatic biota was higher than HMW PAHs. The biota-sediment accumulation factor (BSAF) values of total PAHs in the plants Potamogeton lucens Linn and Ceratophyllum demersum Linn were higher than that in most animals. The BSAF values of total PAHs in animals were in the following order: Cyprinus carpio>Macrobrachium nipponense>Carassius auratus>Channa argus. There was no significant relationship between PAH bioaccumulation and trophic levels in Nansi Lake. Risk assessment of PAHs in water, sediment, and animals indicated that the water environment of Nansi Lake is safe at present. It is worthwhile to note that benzo [a

  11. [Distribution Characteristics and Source Analysis of Polycyclic Aromatic Hydrocarbons (PAHs) in Surface Dust of Xi'an City, China].

    PubMed

    Wang, Li; Wang, Li-jun; Shi, Xing-min; Lu, Xin-wei

    2016-04-15

    A total of 58 surface dust samples were collected from Xi'an city. The concentrations of 16 priority polycyclic aromatic hydrocarbons (PAHs) were analyzed by gas chromatography with a flame ionization detector (GC-FID). At the same time, the distribution and sources of PAHs in surface dust were studied. The results showed that the concentrations of individual PAH ranged from 14.69 to 6370. 48 microg x kg(-1), and the total concentrations of 16 PAHs (∑16 PAHs) ranged from 5039.67 to 47,738.50 microg x kg(-1), with a mean of 13,845.82 microg x kg(-1). Compared to the Y PAHs levels of other cities, the ∑16 PAHs in surface dust of Xi'an belonged to a relatively higher level. PAHs in surface dust were mainly dominated by high molecular weight PAHs with 4-6 rings and the concentration of 7 carcinogenic PAHs (1 CPAHs) accounted for 46.08% of 3 16PAHs. The mean of ∑16 PAHs in surface dust had the highest concentration at industrial area; followed by the educational area, traffic area, business and traffic area; residential area and parks showed relatively lower concentration. The average content of ∑16 PAHs in surface dust presented an increasing trend along the main urban area--the second ring road--the third ring road. ∑16 PAHs in surface dust had higher concentrations at the industrial areas of the east and west suburbs of Xi'an, the south suburb and the north section of the second ring road; ∑16 PAHs concentrations in the main urban area, north suburb and southeast part of Xi'an were relatively lower. The results of ratio, cluster analysis and principal component analysis showed that PAHs in surface dust were mainly originated from the combustion of fossil fuels and coal combustion. Among them, diesel combustion reached 36.07%, gasoline combustion accounted for 32.31%, and coal combustion was resposbe for 23.40% PMID:27548947

  12. Synthesis, anticancer activity, and SAR analyses of compounds containing the 5:7-fused 4,6,8-triaminoimidazo[4,5-e][1,3]diazepine ring system.

    PubMed

    Xie, Min; Lapidus, Rena G; Sadowska, Mariola; Edelman, Martin J; Hosmane, Ramachandra S

    2016-06-15

    Described herein are our limited structure-activity relationship (SAR) studies on a 5:7-fused heterocycle (1), containing the 4,6,8-triaminoimidazo[4,5-e][1,3]diazepine ring system, whose synthesis and potent broad-spectrum anticancer activity we reported a few years ago. Our SAR efforts in this study are mainly focused on judicial attachment of substituents at N-1 and N(6)-positions of the heterocyclic ring. Our results suggest that there is some subtle correlation between the substituents attached at the N-1 position and those attached at the N(6)-position of the heterocycle. It is likely that there is a common hydrophobic binding pocket on the target protein that is occupied by the substituents attached at the N-1 and N(6)-positions of the heterocyclic ligand. This pocket appears to be large enough to hold either a C-18 alkyl chain of N(6) and no attachment at N-1, or a combined C-10 at N(6) and a CH2Ph at N-1. Any alkyl chain shorter or longer than C-10 at N(6) with a CH2Ph attached at N-1, would result in decrease of biological activity. PMID:27134120

  13. Community structure and PAH ring-hydroxylating dioxygenase genes of a marine pyrene-degrading microbial consortium.

    PubMed

    Gallego, Sara; Vila, Joaquim; Tauler, Margalida; Nieto, José María; Breugelmans, Philip; Springael, Dirk; Grifoll, Magdalena

    2014-07-01

    Marine microbial consortium UBF, enriched from a beach polluted by the Prestige oil spill and highly efficient in degrading this heavy fuel, was subcultured in pyrene minimal medium. The pyrene-degrading subpopulation (UBF-Py) mineralized 31 % of pyrene without accumulation of partially oxidized intermediates indicating the cooperation of different microbial components in substrate mineralization. The microbial community composition was characterized by culture dependent and PCR based methods (PCR-DGGE and clone libraries). Molecular analyses showed a highly stable community composed by Alphaproteobacteria (84 %, Breoghania, Thalassospira, Paracoccus, and Martelella) and Actinobacteria (16 %, Gordonia). The members of Thalasosspira and Gordonia were not recovered as pure cultures, but five additional strains, not detected in the molecular analysis, that classified within the genera Novosphingobium, Sphingopyxis, Aurantimonas (Alphaproteobacteria), Alcanivorax (Gammaproteobacteria) and Micrococcus (Actinobacteria), were isolated. None of the isolates degraded pyrene or other PAHs in pure culture. PCR amplification of Gram-positive and Gram-negative dioxygenase genes did not produce results with any of the cultured strains. However, sequences related to the NidA3 pyrene dioxygenase present in mycobacterial strains were detected in UBF-Py consortium, suggesting the representative of Gordonia as the key pyrene degrader, which is consistent with a preeminent role of actinobacteria in pyrene removal in coastal environments affected by marine oil spills. PMID:24356981

  14. Sedimentary records of polycyclic aromatic hydrocarbons (PAHs) in remote lakes across the Tibetan Plateau.

    PubMed

    Yang, Ruiqiang; Xie, Ting; Li, An; Yang, Handong; Turner, Simon; Wu, Guangjian; Jing, Chuanyong

    2016-07-01

    Sediment cores from five lakes across the Tibetan Plateau were used as natural archives to study the time trends of polycyclic aromatic hydrocarbons (PAHs). The depositional flux of PAHs generally showed an increasing trend from the deeper layers towards the upper layer sediments. The fluxes of PAHs were low with little variability before the 1950s, and then gradually increased to the late 1980s, with a faster increasing rate after the 1990s. This temporal pattern is clearly different compared with those remote lakes across the European mountains when PAHs started to decrease during the period 1960s-1980s. The difference of the temporal trend was attributed to differences in the economic development stages and energy structure between these regions. PAHs are dominated by the lighter 2&3-ring homologues with the averaged percentage over 87%, while it is notable that the percentage of heavier 4-6 ring PAHs generally increased in recent years, which suggests the contribution of local high-temperature combustion sources becoming more predominant. PMID:27061469

  15. Rhenium(I) carbonyl complexes of 2,4,6-tris(2-pyridyl)-1,3,5-triazine (TPT). Rhenium(I)-promoted methoxylation of the triazine ring carbon atom in dinuclear rhenium complexes.

    PubMed

    Chen, X; Femia, F J; Babich, J W; Zubieta, J A

    2001-06-01

    2,4,6-Tris(2-pyridyl)-1,3,5-triazine (TPT) bridged dinuclear rhenium(I) tricarbonyl halide complexes with the composition (mu-TPT)[ReX(CO)(3)](2) (3, X = Cl; 4, X = Br) can be made either by one-pot reaction of TPT with 2 equiv of [ReX(CO)(5)] (X = Cl and Br) in chloroform or by reacting mononuclear [ReX(CO)(3)(TPT)] (2) (1, X = Cl; 2, X = Br) with an excess amount of [ReX(CO)(5)]. Crystal data are as follows. 1: monoclinic, P2(1)/c, a = 11.751(1) A, b = 11.376(1) A, c = 15.562(2) A, beta = 103.584(2) degrees, V = 2022.0(4) A(3), Z = 4. 2: monoclinic, P2(1)/c, a = 11.896(1) A, b = 11.396(1) A, c = 15.655(1) A, beta = 104.474(2) degrees, V = 2054.9(3) A(3), Z = 4. 3: triclinic, P1, a = 11.541(2) A, b = 12.119(2) A, c = 13.199(2) A, alpha = 80.377(2) degrees, beta = 76.204(3) degrees, gamma = 66.826(2) degrees, V = 1642.5(4) A(3), Z = 2. Crystals of 4 crystallized from acetone: triclinic, P1, a = 11.586(5) A, b = 12.144(5) A, c = 13.364(6) A, alpha = 80.599(7) degrees, beta = 76.271(8) degrees, gamma = 67.158(8) degrees, V = 1678.0(12) A(3), Z = 2. Crystals of 4' are obtained from CH(2)Cl(2)-pentane solution: monoclinic, C2/c, a = 17.555(4) A, b = 15.277(3) A, c = 13.093(3) A, beta = 111.179(3) degrees, V = 3274.0(12) A(3), Z = 4. By contrast, similar reactions in the presence of methanol yielded complexes with the composition [mu-C(3)N(3)(OMe)(py)(2)(pyH)][ReX(CO)(3)](2) (5, X = Cl; 6, X = Br). Crystal data for 5: monoclinic, C2/c, a = 26.952(2) A, b = 16.602(1) A, c = 14.641(1) A, beta = 116.147(1) degrees, V = 5880.5(8) A(3), Z = 8. 6: monoclinic, C2/c, a = 27.513(3) A, b = 16.740(2) A, c = 14.837(2) A, beta = 116.925(2) degrees, V = 6092.8(10) A(3), Z = 8. An unusual metal-induced methoxylation at the carbon atom of the triazine ring of the bridging TPT ligand was observed. The nucleophilic attack of MeO(-) on C(3) results in a tetrahedral geometry around the carbon atom. Concomitantly, the uncoordinated pyridyl ring is protonated and rotated into a perpendicular

  16. PAH emission from the industrial boilers.

    PubMed

    Li, C; Mi, H; Lee, W; You, W; Wang, Y

    1999-10-01

    Polycyclic aromatic hydrocarbons (PAHs) emitted from 25 industrial boilers were investigated. The fuels used for these 25 boilers included 21 heavy oil, two diesel, a co-combustion of heavy oil and natural gas (HO+NG) and a co-combustion of coke oven gas and blast furnace gas (COG+BFG) boilers. PAH samples from the stack flue gas (gas and particle phases) of these 25 boilers were collected by using a PAH stack sampling system. Twenty one individual PAHs were analyzed primarily by a gas chromatography/mass spectrometer (GC/MS). Total-PAH concentration in the flue gas of 83 measured data for these 25 boiler stacks ranged between 29.0 and 4250 microg/m(3) and averaged 488 microg/m(3). The average of PAH-homologue mass (F%) counted for the total-PAH mass was 54.7%, 9.47% and 15.3% for the 2-ring, 3-ring and 4-ring PAHs, respectively. The PAHs in the stack flue gas were dominant in the lower molecular weight PAHs. The emission factors (EFs) of total-PAHs were 13,300, 2920, 2880 and 208 microg/kg-fuel for the heavy oil, diesel, HO+NG and COG+BFG fueled-boiler, respectively. Nap was the most predominant PAH occurring in the stack flue gas. In addition, the EF of 21 individual PAHs in heavy-oil boiler were almost the highest among the four various fueled-boilers except for those of FL and BkF in the diesel boiler. Furthermore, the EF of total-PAHs or BaP for heavy oil were both one order of magnitude higher than that for the diesel-fueled boiler. PMID:10502602

  17. Determination of polyoxymethylene (POM)--water partition coefficients for oxy-PAHs and PAHs.

    PubMed

    Josefsson, Sarah; Arp, Hans Peter H; Kleja, Dan Berggren; Enell, Anja; Lundstedt, Staffan

    2015-01-01

    Oxygenated polycyclic aromatic hydrocarbons (oxy-PAHs) are a class of ubiquitously occurring pollutants of which little is known. They can be co-emitted with PAHs or formed from PAHs in the environment. The environmental fate and risk of oxy-PAHs are difficult to assess due to a lack of methods to quantify their pore water concentrations. One sampler that can be used to determine freely dissolved concentrations of organic contaminants is polyoxymethylene (POM). In this study, POM - water partition coefficients (KPOM) were determined for 11 oxy-PAHs. KPOM values of 8 PAHs with similar hydrophobicities as the oxy-PAHs were determined for comparison. Results showed that logKPOM values ranged from 2.64 to 4.82 for the PAHs (2-4 rings), similar to previously determined values. LogKPOM values for investigated oxy-PAHs ranged from 0.96 to 5.36. The addition of carbonylic oxygen on a parent PAH generally lowered KPOM by 0.5 to 1.0 log units, which is attributable to the presence of carbonylic oxygens increasing water solubility. The KPOM values presented here will facilitate simultaneous assessments of freely dissolved water concentrations of oxy-PAHs and PAHs in environmental media. PMID:25460771

  18. Rings

    SciTech Connect

    Davis, R.L.

    1989-01-01

    The essence of vortex physics is that at certain low-energy scales elementary excitations of a point particle theory can behave like strings rather than particles. Vortices are the resulting string-like solutions; their thickness sets the distance scale beyond which physics is string-like rather than particle-like. String degrees of freedom are massless in the sense that excitations on a string can have an arbitrarily low frequency. Non-string degrees of freedom correspond to massive particles and are absent from the low energy spectrum. This article considers only field theories with vortices at low energies. The possible existence of a class of solitons in these vortex theories will be discussed. They are vortex rings: they are localized and finite in energy, and able to carry the quantum numbers of point particles. Rings are thus particle-like solutions of a vortex theory, which is itself a limit of a point particle field theory.

  19. Carcinogenic PAH in waterpipe charcoal products

    PubMed Central

    Sepetdjian, Elizabeth; Saliba, Najat; Shihadeh, Alan

    2010-01-01

    Because narghile waterpipe (shisha, hooka) smoking normally involves the use of burning charcoal, smoke inhaled by the user contains constituents originating from the charcoal in addition to those from the tobacco. We have previously found that charcoal accounts for most of the polyaromatic hydrocarbons (PAH) and carbon monoxide in the smoke of the waterpipe, both of which are present in alarming quantities. Because charcoal manufacturing conditions favor formation of PAH, it is reasonable to assume that charcoal sold off the shelf may be contaminated by PAH residues. These residues may constitute a significant fraction of the PAH inhaled by the waterpipe user and those in her/his vicinity. We measured PAH residues on three kinds of raw waterpipe charcoal sampled from Beirut stores and cafés. We found that PAH residues in raw charcoal can account for more than half of the total PAH emitted in the mainstream and sidestream smoke, and about one sixth of the carcinogenic 5- and 6-ring PAH compounds. Total PAH content of the three charcoal types varied systematically by a factor of six from the charcoal with the least to the greatest PAH residue. These findings indicate the possibility of regulating charcoal carcinogen content. PMID:20807559

  20. Carcinogenic PAH in waterpipe charcoal products.

    PubMed

    Sepetdjian, Elizabeth; Saliba, Najat; Shihadeh, Alan

    2010-11-01

    Because narghile waterpipe (shisha, hooka) smoking normally involves the use of burning charcoal, smoke inhaled by the user contains constituents originating from the charcoal in addition to those from the tobacco. We have previously found that charcoal accounts for most of the polyaromatic hydrocarbons (PAH) and carbon monoxide in the smoke of the waterpipe, both of which are present in alarming quantities. Because charcoal manufacturing conditions favor formation of PAH, it is reasonable to assume that charcoal sold off the shelf may be contaminated by PAH residues. These residues may constitute a significant fraction of the PAH inhaled by the waterpipe user and those in her/his vicinity. We measured PAH residues on three kinds of raw waterpipe charcoal sampled from Beirut stores and cafés. We found that PAH residues in raw charcoal can account for more than half of the total PAH emitted in the mainstream and sidestream smoke, and about one sixth of the carcinogenic 5- and 6-ring PAH compounds. Total PAH content of the three charcoal types varied systematically by a factor of six from the charcoal with the least to the greatest PAH residue. These findings indicate the possibility of regulating charcoal carcinogen content. PMID:20807559

  1. Multimedia Model for Polycyclic Aromatic Hydrocarbons (PAHs) and Nitro-PAHs in Lake Michigan

    PubMed Central

    2015-01-01

    Polycyclic aromatic hydrocarbon (PAH) contamination in the U.S. Great Lakes has long been of concern, but information regarding the current sources, distribution, and fate of PAH contamination is lacking, and very little information exists for the potentially more toxic nitro-derivatives of PAHs (NPAHs). This study uses fugacity, food web, and Monte Carlo models to examine 16 PAHs and five NPAHs in Lake Michigan, and to derive PAH and NPAH emission estimates. Good agreement was found between predicted and measured PAH concentrations in air, but concentrations in water and sediment were generally under-predicted, possibly due to incorrect parameter estimates for degradation rates, discharges to water, or inputs from tributaries. The food web model matched measurements of heavier PAHs (≥5 rings) in lake trout, but lighter PAHs (≤4 rings) were overpredicted, possibly due to overestimates of metabolic half-lives or gut/gill absorption efficiencies. Derived PAH emission rates peaked in the 1950s, and rates now approach those in the mid-19th century. The derived emission rates far exceed those in the source inventories, suggesting the need to reconcile differences and reduce uncertainties. Although additional measurements and physiochemical data are needed to reduce uncertainties and for validation purposes, the models illustrate the behavior of PAHs and NPAHs in Lake Michigan, and they provide useful and potentially diagnostic estimates of emission rates. PMID:25373871

  2. [Altitudinal Gradient Distribution and Source Analysis of PAHs Content of Topsoil in Jinfo Mountain, Chongqing].

    PubMed

    Shi, Yang; Sun, Yu-chuan; Liang, Zuo-bing; Ren, Kun; Yuan, Dao-xian

    2015-04-01

    The condensation effect has made high mountains the storage vault of durable organic pollutants. This research measured the content and constitutes of polycyclic aromatic hydrocarbons (PAHs) in 10 topsoil samples collected at different altitudes from the south slope of Chongqing Jinfo Mountain by gas chromatograph-mass spectrometer (GC/MC). And the pollution source of PAHs was analyzed by ratio method and principal component regression. The ecological risk of PAHs was evaluated using BaP toxic equivlants (TEQ(BaP)) The results showed that the concentrations of 16 priority PAHs in topsoil ranged from 240-2 121 ng x g(-1). The average value of PAHs was 849 ng x g(-1), and 2 to 3-ring PAHs were the dominant compounds. The concentrations of 7 carcinogenic PAHs accounted for 17.8% of total PAHs averagely. In the research area, various-ring PAHs and gross PAHs increased with the rise of altitude. The increase of low-ring PAHs was most obvious, and the volatility of high-ring PAHs was relatively high. But the ratio of different-ring PAHs in gross PAHs showed no regularity with the rise of altitude. The PAHs of soil in the research area mainly came from the oil sources, oil products, and combustion sources of coal and biomass. In the research area, the soil has been polluted to a certain extent, but the toxicity risk is relatively low. PMID:26164921

  3. Airborne particulate polycyclic aromatic hydrocarbon (PAH) pollution in a background site in the North China Plain: concentration, size distribution, toxicity and sources.

    PubMed

    Zhu, Yanhong; Yang, Lingxiao; Yuan, Qi; Yan, Chao; Dong, Can; Meng, Chuanping; Sui, Xiao; Yao, Lan; Yang, Fei; Lu, Yaling; Wang, Wenxing

    2014-01-01

    The size-fractionated characteristics of particulate polycyclic aromatic hydrocarbons (PAHs) were studied from January 2011 to October 2011 using a Micro-orifice Uniform Deposit Impactor (MOUDI) at the Yellow River Delta National Nature Reserve (YRDNNR), a background site located in the North China Plain. The average annual concentration of total PAHs in the YRDNNR (18.95 ± 16.51 ng/m(3)) was lower than that in the urban areas of China; however, it was much higher than that in other rural or remote sites in developed countries. The dominant PAHs, which were found in each season, were fluorene (5.93%-26.80%), phenanthrene (8.17%-26.52%), fluoranthene (15.23%-27.12%) and pyrene (9.23%-16.31%). A bimodal distribution was found for 3-ring PAHs with peaks at approximately 1.0-1.8 μm and 3.2-5.6 μm; however, 4-6 ring PAHs followed a nearly unimodal distribution, with the highest peak in the 1.0-1.8 μm range. The mass median diameter (MMD) values for the total PAHs averaged 1.404, 1.467, 1.218 and 0.931 μm in spring, summer, autumn and winter, respectively. The toxicity analysis indicated that the carcinogenic potency of particulate PAHs existed primarily in the <1.8 μm size range. Diagnostic ratios and PCA analysis indicated that the PAHs in aerosol particles were mainly derived from coal combustion. In addition, back-trajectory calculations demonstrated that atmospheric PAHs were produced primarily by local anthropogenic sources. PMID:23921366

  4. A hierarchical approach measures the aerial extent and concentration levels of PAH-contaminated shoreline sediments at historic industrial sites in Prince William Sound, Alaska.

    PubMed

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

    2006-04-01

    A field study was conducted in 2003 to estimate the areal distribution and concentrations of polycyclic aromatic hydrocarbons (PAH) in intertidal sediments at sites of past human and industrial activity (HA sites) in Prince William Sound (PWS), Alaska, the site of the 1989 Exxon Valdez oil spill. More than 50 HA sites, primarily in western PWS, were identified through analysis of historic records and prior field studies, and nine sites were selected for detailed surveys. The areal assessment process consisted of seven steps: (1) identify site from historic records and field surveys; (2) locate visual evidence of surface oil/tar at a site; (3) prepare a site map and lay out a sampling grid over the entire site with 10-m grid spacing; (4) excavate pits to 50 cm depth on the grid; (5) perform a field colorimetric test to estimate total PAH (TPAH) in sediments from the wall of each pit and record the results in the ranges <1 ppm; 1-10 ppm; >10 ppm TPAH; (6) expand grid size if necessary if elevated PAH levels are detected colorimetrically; (7) select 20 samples from each site for same-day shipboard PAH analysis by immunoassay (SDI RaPID PAH) and, based on these results, select sediment samples from each site for full PAH analysis in the laboratory to identify PAH sources. A total of 416 pits were dug at the nine sites. Nine acres of sediments with TPAH >2500 ppb dry wt. were mapped at the nine sites. TPAH concentrations obtained by immunochemical analysis of 181 samples from the nine sites ranged from 20 to 1,320,000 ppb (wet wt.). The contaminants are mixtures of petroleum products (2-3 ring PAH) and combustion products (4-6 ring PAH) unrelated to the 1989 Exxon Valdez oil spill. Mussels and clams collected at these sites have elevated levels of PAH that are compositionally similar to the PAH in the sediments. These findings indicate that at least a portion of the sediment PAH is bioavailable. The PAH sources at these historic industrial sites are chronic. They

  5. Anionic-nonionic mixed-surfactant-enhanced remediation of PAH-contaminated soil.

    PubMed

    Shi, Zhentian; Chen, Jiajun; Liu, Jianfei; Wang, Ning; Sun, Zheng; Wang, Xingwei

    2015-08-01

    Soil washing is an efficient remediation technique that enhances the solubility of polycyclic aromatic hydrocarbons (PAHs) in specific surfactant to remediate PAH-contaminated soil. This study evaluated the remediation efficiency of PAH-contaminated soil from a coke oven plant by comparing sodium dodecyl sulfate (SDS), sodium dodecylbenzene sulfonate (SDBS), and Triton X-100 (TX100), as well as TX100-SDS and TX100-SDBS mixed surfactants. Results showed that SDS-TX100 and SDBS-TX100 had synergistic effects on PAH solubilization when surfactant concentrations were above their critical micelle concentration. Competitive effects of the three solubilized PAHs (phenanthrene with three rings, fluoranthene with four rings, and benzo[a]pyrene with five rings) with a particular anionic-nonionic mixed surfactant were investigated. PAHs with more rings were found to slightly decrease the solubility in surfactant solution of PAHs with fewer rings, whereas PAHs with fewer rings promoted the solubility in surfactant solution of PAHs with more rings. The removal ratios of PAHs during the remediation of actual PAH-contaminated soil were best improved by the anionic-nonionic mixed surfactant TX100-SDS (9:1), followed by TX100-SDS (8:2), TX100-SDS (7:3), TX100-SDBS (7:3), TX100, SDBS, and SDS. Therefore, anionic-nonionic mixed surfactants can help improve the remediation performance of PAHs based on their application in tests of cleaning actual PAH-contaminated soil from a coke oven plant. PMID:26002358

  6. 2,4,6-Trichlorophenol

    Integrated Risk Information System (IRIS)

    2,4,6 - Trichlorophenol ; CASRN 88 - 06 - 2 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcino

  7. Oxidative biodegradation pathways of PAHs

    SciTech Connect

    Cerniglia, C.E.

    1993-12-31

    Polycyclic aromatic hydrocarbons (PAHs) constitute a class of hazardous organic chemical consisting of three of more fused benzene rings in linear, angular and cluster arrangements. PAHs mostly occur as a result of fossil fuel combustion, as by-product of industrial processing and during the cooking of foods. A catabolically diverse microbial community, consisting of bacteria, fungi and algae, metabolizes aromatic compounds. Molecular oxygen is essential for the initial hydroxylation of polycyclic aromatic hydrocarbons by microorganisms. In contrast to bacteria, filamentous fungi use hydroxylation as a prelude to detoxification rather than to catabolism and assimilation. The biochemical principles underlying the degradation of polycyclic aromatic hydrocarbons will be discussed. The oxidative pathways of polycyclic aromatic hydrocarbon catabolism will be discussed. Studies will be presented on the relationship between the chemical structure of the polycyclic aromatic hydrocarbon and the rate of polycyclic aromatic hydrocarbon biodegradation in aquatic and terrestrial ecosystems.

  8. PAH determination based on a rapid and novel gas purge-microsyringe extraction (GP-MSE) technique in road dust of Shanghai, China: Characterization, source apportionment, and health risk assessment.

    PubMed

    Zheng, Xin; Yang, Yi; Liu, Min; Yu, Yingpeng; Zhou, John L; Li, Donghao

    2016-07-01

    A novel cleanup technique termed as gas purge-microsyringe extraction (GP-MSE) was evaluated and applied for polycyclic aromatic hydrocarbon (PAH) determination in road dust samples. A total of 68 road dust samples covering almost the entire Shanghai area were analyzed for 16 priority PAHs using gas chromatography-mass spectrometry. The results indicate that the total PAH concentrations over the investigated sites ranged from 1.04μg/g to 134.02μg/g dw with an average of 13.84μg/g. High-molecular-weight compounds (4-6 rings PAHs) were significantly dominant in the total mass of PAHs, and accounted for 77.85% to 93.62%. Diagnostic ratio analysis showed that the road dust PAHs were mainly from the mixture of petroleum and biomass/coal combustions. Principal component analysis in conjunction with multiple linear regression indicated that the two major origins of road dust PAHs were vehicular emissions and biomass/fossil fuel combustions, which contributed 66.7% and 18.8% to the total road dust PAH burden, respectively. The concentration of benzo[a]pyrene equivalent (BaPeq) varied from 0.16μg/g to 24.47μg/g. The six highly carcinogenic PAH species (benz(a)anthracene, benzo(a)pyrene, benzo(b)fluoranthene, benzo(k)fluoranthene, dibenz(a,h)anthracene, and indeno(1,2,3-cd)pyrene) accounted for 98.57% of the total BaPeq concentration. Thus, the toxicity of PAHs in road dust was highly associated with high-molecular-weight compounds. PMID:27037890

  9. Environmental stability of PAH source indices in pyrogenic tars

    SciTech Connect

    Uhler, A.D.; Emsbo-Mattingly, S.D.

    2006-04-15

    Polycyclic aromatic hydrocarbons (PAHs) are widespread environmental contaminants found in soil, sediments, and airborne particulates. The majority of PAHs found in modern soils and sediments arise from myriad anthropogenic petrogenic and pyrogenic sources. Tars and tar products such as creosote produced from the industrial pyrolysis of coal or oil at former manufactured gas plants (MGPs) or in coking retorts are viscous, oily substances that contain significant concentrations of PAH, usually in excess of 30% w/w. Pyrogenic tars and tar products have unique PAH patterns (source signatures) that are a function of their industrial production. Among pyrogenic materials, certain diagnostic ratios of environmentally recalcitrant 4-, 5- and 6-ring PAHs have been identified as useful environmental markers for tracking the signature of tars and petroleum in the environment. The use of selected PAH source ratios is based on the concept that PAHs with similar properties (i.e., molecular weight, partial pressure, solubility, partition coefficients, and biotic/abiotic degradation) will weather at similar rates in the environment thereby yielding stable ratios. The stability of more than 30 high molecular weight PAH ratios is evaluated during controlled studies of tar evaporation and aerobic biodegradation. The starting materials in these experiments consisted of relatively unweathered tars derived from coal and petroleum, respectively. The PAH ratios from these laboratory studies are compared to those measured in PAH residues found in tar-contaminated soils at a former MGP that operated with a carburetted water gas process.

  10. Polycyclic aromatic hydrocarbons (PAH) formation from the pyrolysis of different municipal solid waste fractions

    SciTech Connect

    Zhou, Hui; Wu, Chunfei; Onwudili, Jude A.; Meng, Aihong; Zhang, Yanguo; Williams, Paul T.

    2015-02-15

    Highlights: • PAH from pyrolysis of 9 MSW fractions was investigated. • Pyrolysis of plastics released more PAH than that of biomass. • Naphthalene was the most abundant PAH in the tar. • The mechanism of PAH release from biomass and plastics was proposed. - Abstract: The formation of 2–4 ring polycyclic aromatic hydrocarbons (PAH) from the pyrolysis of nine different municipal solid waste fractions (xylan, cellulose, lignin, pectin, starch, polyethylene (PE), polystyrene (PS), polyvinyl chloride (PVC), and polyethylene terephthalate (PET)) were investigated in a fixed bed furnace at 800 °C. The mass distribution of pyrolysis was also reported. The results showed that PS generated the most total PAH, followed by PVC, PET, and lignin. More PAH were detected from the pyrolysis of plastics than the pyrolysis of biomass. In the biomass group, lignin generated more PAH than others. Naphthalene was the most abundant PAH, and the amount of 1-methynaphthalene and 2-methynaphthalene was also notable. Phenanthrene and fluorene were the most abundant 3-ring PAH, while benzo[a]anthracene and chrysene were notable in the tar of PS, PVC, and PET. 2-ring PAH dominated all tar samples, and varied from 40 wt.% to 70 wt.%. For PS, PET and lignin, PAH may be generated directly from the aromatic structure of the feedstock.

  11. Sources, fate, and effects of PAHs in shallow water environments: a review with special reference to small watercraft

    USGS Publications Warehouse

    Albers, P.H.

    2002-01-01

    Polycyclic aromatic hydrocarbons (PAHs) are aromatic hydrocarbons with two to seven fused carbon (benzene) rings that can have substituted groups attached. Shallow coastal, estuarine, lake, and river environments receive PAHs from treated wastewater, stormwater runoff, petroleum spills and natural seeps, recreational and commercial boats, natural fires, volcanoes, and atmospheric deposition of combustion products. Abiotic degradation of PAHs is caused by photooxidation, photolysis in water, and chemical oxidation. Many aquatic microbes, plants, and animals can metabolize and excrete ingested PAHs; accumulation is associated with poor metabolic capabilities, high lipid content, and activity patterns or distributions that coincide with high concentrations of PAHs. Resistance to biological transformation increases with increasing number of carbon rings. Four- to seven-ring PAHs are the most difficult to metabolize and the most likely to accumulate in sediments. Disturbance by boating activity of sediments, shorelines, and the surface microlayer of water causes water column re-entry of recently deposited or concentrated PAHs. Residence time for PAHs in undisturbed sediment exceeds several decades. Toxicity of PAHs causes lethal and sublethal effects in plants and animals, whereas some substituted PAHs and metabolites of some PAHs cause mutations, developmental malformations, tumors, and cancer. Environmental concentrations of PAHs in water are usually several orders of magnitude below levels that are acutely toxic, but concentrations can be much higher in sediment. The best evidence for a link between environmental PAHs and induction of cancerous neoplasms is for demersal fish in areas with high concentrations of PAHs in the sediment.

  12. Polycyclic aromatic hydrocarbon (PAHs) pollutants in groundwater from coal gangue stack area: characteristics and origin.

    PubMed

    Wang, X W; Zhong, N N; Hu, D M; Liu, Z Z; Zhang, Z H

    2009-01-01

    The concentrations of polycyclic aromatic hydrocarbons (PAHs) in the leachate from the gangue and 20 groundwater samples, which were collected from the 12th Coal Mine around gangue piles in Henan Province, China, were determined by SPE-GC-MS. The characteristics of PAHs pollutants in groundwater were investigated, and compared with the concentrations of PAHs in the leachate from different weathered gangues to discuss the pollution effects of PAHs from coal gangue on groundwater. The results showed that total concentrations of the 16 EPA preferentially controlled PAHs ranged from 146.9 ng/L to 1220.6 ng/L.The components of PAHs such as chrysene, benzo[a]anthracene, benzo[b + k]fluoranthene, indeno[1,2,3-c,d]-pyrene, and dibenz[a,h]anthracene were fairly high. The 2-4 rings PAHs such as naphthalene, phenanthrene, fluorene and chrysene were dominant in groundwater, which was similar to those of the leachate from the different weathered gangues. Therefore, it should be paid much more attention on the transport of lower ring numbered PAHs leached by rains from the coal mines after landfilling and dumping. Based on the spatial distribution of PAHs and the high concentrations of PAHs with 2-4 rings in groundwater and leaching samples, there might be other pollution sources of PAHs except for penetration from coal gangue into groundwater in the Pingdingshan coal mine area. PMID:19273905

  13. Polycyclic aromatic hydrocarbons (PAHs) in water from three estuaries of China: Distribution, seasonal variations and ecological risk assessment.

    PubMed

    Yan, Jinxia; Liu, Jingling; Shi, Xuan; You, Xiaoguang; Cao, Zhiguo

    2016-08-15

    The distribution, seasonal variations and ecological risk assessment of polycyclic aromatic hydrocarbons (PAHs) in water from three estuaries in Hai River Basin of China, which has been suffering from different anthropogenic pressures, were investigated. In three estuaries, the average concentration of ΣPAHs was the lowest in Luan River estuary, followed by Hai River estuary, and the highest in Zhangweixin River estuary. There were significant seasonal variations in ΣPAHs, the concentrations of ΣPAHs were higher in November than in May and August. The composition profiles of PAHs in different sites were significantly different, and illustrated seasonal variations. Generally, 2-ring (Nap) and 3-ring PAHs (Acp, Fl and Phe) were the most abundant components at most sampling sites in three estuaries. The PAHs in three estuaries were mainly originated from pyrogenic sources. A method based on toxic equivalency factors (TEFs) and risk quotient (RQ) was proposed to assess the ecological risk of ΣPAHs, with the ecological risk of individual PAHs being considered separately. The results showed that the ecological risks caused by ΣPAHs were high in Hai River estuary and Zhangweixin River estuary, and moderate in Luan River estuary. The mean values of ecological risk in August were lower than those in November. The contributions of individual PAHs to ecological risk were different in May, August and November. 3-ring and 4-ring PAHs accounted for much more ecological risk than 2-ring, 5-ring and 6-ring, although the contributions of 5-ring and 6-ring to ecological risk were higher than these to PAHs concentrations. PMID:27209122

  14. METABOLIC ACTIVATION PATHWAYS OF CYCLOPENTA-FUSED PAH (POLYCYCLIC AROMATIC HYDROCARBONS) AND THEIR RELATIONSHIP TO GENETIC AND CARCINOGENIC ACTIVITY

    EPA Science Inventory

    Cyclopenta-fused PAH are a novel class of environmental PAH of which the most well known example is cyclopenta(cd)pyrene. The fusion of an unsaturated cyclopenta-ring on a PAH in general, markedly enhances its activity as a gene mutagen in bacteria and cultured mammalian cells, a...

  15. Distribution characteristics and source apportionment of polycyclic aromatic hydrocarbons (PAHs) in the Liao River drainage basin, northeast China.

    PubMed

    Hu, Jian; Liu, Congqiang; Zhang, Guoping; Zhang, Yanlin; Li, Siliang; Zhao, Zhiqi; Liu, Baojian; Guo, Qinjun

    2016-04-01

    The Liao River drainage basin, which is one of China's seven major rivers basins, is located in northeast China. This region is characterized by important industrial bases including steel factories and oil and chemical plants, all of which have the potential to contribute pollutants to the drainage basin. In this study, 16 polycyclic aromatic hydrocarbons (PAHs) in water and suspended particulate matter (SPM) in the major rivers of the Liao River drainage basin were identified and quantified by gas chromatography mass spectrometry (GC/MS). The total PAH concentrations ranged from 0.4 to 76.5 μg/g (dry weight) in SPM and 32.6 to 108 ng/L in surface water, respectively. Low-ring PAHs (including two- and three-ring PAHs) were dominant in all PAH samples, and the level of low-ring PAHs in surface water was higher than that in SPM. The proportion of two-ring PAHs was the highest, accounting for an average of 68.2 % of the total PAHs in surface water, while the level of three-ring PAHs was the highest in SPM, with an average of 66.3 %. When compared with other river systems, the concentrations of PAHs in the Liao River drainage basin were lower. Identification of the emission sources based on diagnostic ratios suggested petroleum and fossil fuel combustion were important contribution to PAHs in the study area. PMID:26972927

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

    PubMed

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

    2013-03-01

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

  17. Laboratory Astrochemistry: Interstellar PAHs

    NASA Technical Reports Server (NTRS)

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

    2000-01-01

    Polycyclic aromatic hydrocarbons (PAHs) are now considered to be an important and ubiquitous component of the organic material in space. PAHs are found in a large variety of extraterrestrial materials such as interplanetary dust particles (IDPs) and meteoritic materials. PAHs are also good candidates to account for the infrared emission bands (UIRs) and the diffuse interstellar optical absorption bands (DIBs) detected in various regions of the interstellar medium. The recent observations made with the Infrared Space Observatory (ISO) have confirmed the ubiquitous nature of the UIR bands and their carriers. PAHs are thought to form through chemical reactions in the outflow from carbon-rich stars in a process similar to soot formation. Once injected in the interstellar medium, PAHs are further processed by the interstellar radiation field, interstellar shocks and energetic particles. A major, dedicated, laboratory effort has been undertaken to measure the physical and chemical characteristics of these complex molecules and their ions under experimental conditions that mimic the interstellar conditions. These measurements require collision-free conditions where the molecules and ions are cold and chemically isolated. The spectroscopy of PAHs under controlled conditions represents an essential diagnostic tool to study the evolution of extraterrestrial PAHs. The Astrochemistry Laboratory program will be discussed through its multiple aspects: (1) objectives, (2) approach and techniques adopted, (3) adaptability to the nature of the problem(s), and (4) results and implications for astronomy as well as for molecular spectroscopy. A review of the data generated through laboratory simulations of space environments and the role these data have played in our current understanding of the properties of interstellar PAHs will be presented. The discussion will also introduce the newest generation of laboratory experiments that are currently being developed in order to provide a

  18. PAH FIR Spectroscopy

    NASA Astrophysics Data System (ADS)

    Mattioda, Andrew; Ricca, A.; Tucker, J.; Bauschlicher, C., Jr.; Allamandola, L.

    2009-01-01

    The mid-IR spectra of a majority of astronomical sources are dominated by emission features near 3.3, 6.2, 7.7, and 11.2 µm. These features, formerly referred to as the Unidentified Infrared (UIR) Bands, are now generally thought to originate in free polycyclic aromatic hydrocarbon (PAH) molecules and closely related species. In addition to dominating the 3-20 µm region of the spectrum, they carry some 20-40% of the total IR luminosity from most of these objects. PAHs dominate the mid-IR emission from many galactic and extragalactic objects. As such, this material tracks a wide variety of astronomical processes, making this spectrum a powerful probe of the cosmos Apart from bands in the mid-IR, PAHs have bands spanning the Far-IR (20 to 1000 mm) and these FIR features should be present in astronomical sources. However, with one exception, the FIR spectral characteristics are known only for a few neutral small PAHs trapped in salt pellets or oils at room temperature, data which is not relevant to astrophysics. Furthermore, since most emitting PAHs responsible for the mid-IR astronomical features are ionized, the absence of any experimental or theoretical PAH ion FIR spectra will make it impossible to correctly interpret the FIR data from these objects. In view of the upcoming Herschel space telescope mission and SOFIA's FIR airborne instrumentation, which will pioneer the FIR region, it is now urgent to obtain PAH FIR spectra. This talk will present an overview of the FIR spectroscopy of PAHs.

  19. Accumulation of weathered polycyclic aromatic hydrocarbons (PAHs) by plant and earthworm species.

    PubMed

    Parrish, Zakia D; White, Jason C; Isleyen, Mehmet; Gent, Martin P N; Iannucci-Berger, William; Eitzer, Brian D; Kelsey, Jason W; Mattina, Maryjane Incorvia

    2006-07-01

    Experiments were conducted to assess the bioavailability of polyclycic aromatic hydrocarbons (PAHs) in soil from a Manufactured Gas Plant site. Three plant species were cultivated for four consecutive growing cycles (28 days each) in soil contaminated with 36.3 microg/g total PAH. During the first growth period, Cucurbita pepo ssp. pepo (zucchini) tissues contained significantly greater quantities of PAHs than did Cucumis sativus (cucumber) and Cucurbita pepo ssp. ovifera (squash). During the first growth cycle, zucchini plants accumulated up to 5.47 times more total PAH than did the other plants, including up to three orders of magnitude greater levels of the six ring PAHs. Over growth cycles 2-4, PAH accumulation by zucchini decreased by 85%, whereas the uptake of the contaminants by cucumber and squash remained relatively constant. Over all four growth cycles, the removal of PAHs by zucchini was still twice that of the other species. Two earthworm species accumulated significantly different amounts of PAH from the soil; Eisenia foetida and Lumbricus terrestris contained 0.204 and 0.084 microg/g total PAH, respectively, but neither species accumulated measurable quantities 5 or 6 ring PAHs. Lastly, in abiotic desorption experiments with an aqueous phase of synthetically prepared organic acid solutions, the release of 3 and 4 ring PAHs from soil was unaffected by the treatments but the desorption of 5-6 ring constituents was increased by up to two orders of magnitude. The data show that not only is the accumulation of weathered PAHs species-specific but also that the bioavailability of individual PAH constituents is highly variable. PMID:16337258

  20. Distribution, partition and removal of polycyclic aromatic hydrocarbons (PAHs) during coking wastewater treatment processes.

    PubMed

    Zhang, Wanhui; Wei, Chaohai; An, Guanfeng

    2015-05-01

    In this study, we report the performance of a full-scale conventional activated sludge (A-O1-O2) treatment in eliminating polycyclic aromatic hydrocarbons (PAHs). Both aqueous and solid phases along with the coking wastewater treatment processes were analyzed for the presence of 18 PAHs. It was found that the target compounds occurred widely in raw coking wastewater, treated effluent and sludge samples. In the coking wastewater treatment system, 4-5 ring PAHs were the dominant compounds, while 4 rings PAHs predominated in the sludge samples. Over 98% of the PAH removal was achieved in the coking wastewater treatment plant (WWTP), with the total concentration of PAHs being 21.3 ± 1.9 μg L(-1) in the final effluent. During the coking wastewater treatment processes, the association of the lower molecular weight PAH with suspended solids was generally less than 60%, while the association of higher molecular weight PAHs was greater than 90%. High distribution efficiencies (Kdp and Kds) were found, suggesting that adsorption was the potential removal pathway of PAHs. Finally, the mass balances of PAHs in various stages of the coking WWTP were obtained, and the results indicated that adsorption to sludge was the main removal pathway for PAHs in the coking wastewater treatment processes. PMID:25865172

  1. Spatial Distribution of Polycyclic Aromatic Hydrocarbon (PAH) Concentrations in Soils from Bursa, Turkey.

    PubMed

    Karaca, Gizem

    2016-02-01

    The objectives of this study were to identify regional variations in soil polycyclic aromatic hydrocarbon (PAH) contamination in Bursa, Turkey, and to determine the distributions and sources of various PAH species and their possible sources. Surface soil samples were collected from 20 different locations. The PAH concentrations in soil samples were analyzed using gas chromatography-mass spectrometry (GC-MS). The total PAH concentrations (∑12 PAH) varied spatially between 8 and 4970 ng/g dry matter (DM). The highest concentrations were measured in soils taken from traffic+barbecue+ residential areas (4970 ng/g DM) and areas with cement (4382 ng/g DM) and iron-steel (4000 ng/g DM) factories. In addition, the amounts of ∑7 carcinogenic PAH ranged from 1 to 3684 ng/g DM, and between 5 and 74 % of the total PAHs consisted of such compounds. Overall, 4-ring PAH compounds (Fl, Pyr, BaA and Chr) were dominant in the soil samples, with 29-82 % of the ∑12 PAH consisting of 4-ring PAH compounds. The ∑12 BaPeq values ranged from 0.1 to 381.8 ng/g DM. Following an evaluation of the molecular diagnostic ratios, it was concluded that the PAH pollution in Bursa soil was related to pyrolytic sources; however, the impact of petrogenic sources should not be ignored. PMID:26658619

  2. Bioaccumulation, biotransformation and DNA binding of PAHs in feral eel (Anguilla anguilla) exposed to polluted sediments: A field survey

    SciTech Connect

    Oost, R. Van Der; Heida, H.; Satumalay, K. ); Schooten, F.J. Van . Dept. of Health Risk Analysis and Toxicology); Ariese, F.; Vermeulen, N.P.E. )

    1994-06-01

    Samples of sediment and eel taken from six sites in Amsterdam with different levels of water pollution were analyzed for 16 parental PAHs. In addition, biliary PAH metabolites and hepatic PAH-DNA adducts were determined in the eel to evaluate biomonitoring techniques for PAH exposure. There was a clear difference between PAH profiles in sediments and eel. Mainly two- and three-ring PAHs were detected in eel, whereas four-ring PAHs predominated in the sediments. Because PAH bioaccumulation was highest in eel from the reference sites, tissue levels of the parental PAH are probably not the most accurate monitor of PAH exposure in fish. An elevated excretion of 1-OH pyrene (determined by synchronous scan fluorescence) was observed in the bile of fish from three of the four polluted sites, indicating that this parameter may be used as a biomarker for PAH exposure. A significant increase in PAH-DNA adduct levels was observed in the liver of eel from all polluted sites. Therefore, this parameter seems to be a sensitive biomarker for exposure to mutagenic and carcinogenic PAHs.

  3. Emissions of polycyclic aromatic hydrocarbons (PAHs) from the pyrolysis of scrap tires

    NASA Astrophysics Data System (ADS)

    Chen, Shui-Jen; Su, Hung-Bin; Chang, Juu-En; Lee, Wen-Jhy; Huang, Kuo-Lin; Hsieh, Lien-Te; Huang, Yi-Chu; Lin, Wen-Yinn; Lin, Chih-Chung

    This work investigated the PAHs generated in a waste-tire pyrolysis process and the PAHs removal by a wet scrubber (WSB) and a flare. IND, DBA, and BaP were found to dominate in the powders of scrap tires before the pyrolysis. The PAHs in the carbon blacks formed in the pyrolysis were mainly 2-, 3-, 6-, and 7-ring PAHs. Nap was the most predominant water-phase PAH in the WSB effluent. About 40% of the water-phase total-PAHs in the WSB effluent were contributed by nine carcinogenic PAHs. NaP, IND, and COR displayed higher mean gas- and particulate-phase concentrations than the other PAHs in the flare exhaust. The mean removal efficiencies of individual PAHs, total-PAHs, and high carcinogenic BaP+IND+DBA were 39.1-90.4%, 76.2%, and 84.9%, respectively for the WSB. For the flare, the mean removal efficiencies of gaseous, particulate, and combined (gaseous+particulate) total-PAHs were 59.8%, 91.2%, and 66.8%, respectively, whereas the removal efficiencies were 91.0%, 80.1%, and 89.1%, respectively for the total-BaPeq. However, the gaseous BaA displayed a negative mean removal efficiency. The total PAH emission rate and factor estimated for the scrap tire pyrolysis plant were 42.3 g d -1 and 4.00 mg kg-tire -1, respectively.

  4. PAHs contamination in bank sediment of the Yamuna river, Delhi, India.

    PubMed

    Agarwal, Tripti; Khillare, P S; Shridhar, Vijay

    2006-12-01

    This study was performed to elucidate the distribution, concentration trend and possible sources of PAHs in bank sediment of river Yamuna in Delhi, India. The levels of 16 priority polycyclic aromatic hydrocarbons (PAHs) were analyzed during pre-monsoon, monsoon and post-monsoon seasons in the sediment fraction < 53 microm. Reference standards and internal standards were used for identification and quantification of PAHs by HPLC. The sum of 16 PAH compounds ranged from 4.50 to 23.53 microg/g with a mean concentration of 10.15 +/- 4.32 microg/g (dry wt.). Among 5 sites studied, the site, Income Tax Office (ITO) was found to be the hotspot attaining highest concentration. Predominance of 2-4 ring PAHs suggests a relatively recent local sources of PAHs in the study area. Moreover, molecular indices based source apportionment also illustrates pyrogenic source fingerprint of PAHs. No significant temporal trend was observed. PMID:16763739

  5. Ecotoxicological risk of polycyclic aromatic hydrocarbons (PAHs) in urban soil of Isfahan metropolis, Iran.

    PubMed

    Moore, F; Akhbarizadeh, R; Keshavarzi, B; Khabazi, S; Lahijanzadeh, A; Kermani, M

    2015-04-01

    Concentration, distribution, probable sources, and health risks of 16 polycyclic aromatic hydrocarbons (PAHs) were investigated in 52 soil samples collected within a radius 50 km from Isfahan metropolis center. Total concentration of PAHs ranged from 57.70 to 11,730.08 μg/kg averaging 2,000.56 μg/kg. Spatial PAH profiles were site-specific and higher concentration of PAHs was observed in the vicinity of industrial zones within Isfahan metropolis. The molecular indices, ring classes, and principal component analysis indicated that the sources of PAHs were both geogenic and pyrogenic. The incremental lifetime cancer risks of exposure to soil PAHs for adults and children living in the study area were 2.3×10(-2) and 2.2×10(-3), respectively. The results suggest that current PAHs levels in Isfahan metropolis soil are highly carcinogenic and may hold a serious health risk for local resident. PMID:25805371

  6. 2,4,6-Trinitrotoluene (TNT)

    Integrated Risk Information System (IRIS)

    2,4,6 - Trinitrotoluene ( TNT ) ; CASRN 118 - 96 - 7 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for N

  7. 2,3,4,6-Tetrachlorophenol

    Integrated Risk Information System (IRIS)

    2,3,4,6 - Tetrachlorophenol ; CASRN 58 - 90 - 2 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncar

  8. Career Education: Grades 4-6.

    ERIC Educational Resources Information Center

    Cortland-Madison Board of Cooperative Educational Services, Cortland, NY.

    The third of a series of nine career education guides includes four social studies units for grades 4-6. Part one, famous Americans from Plymouth Rock to Tranquility Base, includes goals, objectives, skills to be taught or reviewed, lists of famous Americans in the fields of science and medicine, inventions, sports, religion, politics, literature,…

  9. Science for Children, 4-6.

    ERIC Educational Resources Information Center

    New York State Education Dept., Albany. Bureau of General Education Curriculum Development.

    This publication developed by the New York State Education Department with the cooperation of the University of the State of New York, is a curriculum guide for elementary science (grade 4-6). This guide is organized around 6 large subject areas: (1) Living things; (2) Our growing bodies; (3) Air, water and weather; (4) The earth and its…

  10. A Dogrib History. Grade 4-6.

    ERIC Educational Resources Information Center

    Fraser, Tara

    A publication on the history and traditional lifestyle of the Dogrib Tribe of Canada's Northwest Territories is intended for use in grades 4-6. The text is illustrated with numerous drawings. Sections describe the caribou, spruce tree, muskox, fox, ducks and geese and their usefulness to Dogrib people. Activities covered are trading at the trading…

  11. Spatial distribution and seasonal variation of polycyclic aromatic hydrocarbons (PAHs) contaminations in surface water from the Hun River, Northeast China.

    PubMed

    Zhang, Hongling; Sun, Lina; Sun, Tieheng; Li, Huiying; Luo, Qing

    2013-02-01

    The objectives of this study were to investigate the levels, dispersion patterns, seasonal variation, and sources of 16 priority polycyclic aromatic hydrocarbons (16 EPA-PAHs) in the Hun River of Liaoning Province, China. Samples of surface water were collected from upstream to downstream locations, and also from the main tributaries of the Hun River in dry period, flood period, and level period, respectively. After appropriate preparation, all samples were analyzed for 16 EPA-PAHs. Total PAHs concentrations varied from 124.55 to 439.27 ng l(-1) in surface water in dry period, 1,615.75 to 5,270.04 ng l(-1) in flood period, and 2,247.42 to 7,767.9 ng l(-1) in level period. The 16 EPA-PAHs concentrations were significantly increased in the order of level period > flood period > dry period. The composition pattern of PAHs in surface water was dominated by low molecular weight PAHs, in particular two- to three-ring PAHs. In addition, two-ring PAH accounted for 39.33 to 88.27 % of the total PAHs in level period. Low molecular weight PAHs predomination together with higher levels of PAHs in flood and level period suggested a relatively recent local source of PAHs. Special PAHs ratios such as phenanthrene/anthracene and fluoranthene/pyrene indicated that under dry weather season conditions, the PAHs found in surface water were primarily from petrogenic source, while under wet weather season conditions they were from mixed source of both petrogenic inputs and combustion sources. The comparison of PAHs contamination among different types of areas in China suggested that atmospheric depositions might be the most important approaches of PAHs into water system. Although the Hun River exists low PAHs ecological risk now, potential toxic effects will be existed in the future especially in flood and level period. PMID:22527471

  12. 1,2,3,3',4',6'-Hexaacetyl-4,6-O-benzyl-idenesucrose.

    PubMed

    Brito-Arias, Marco A; Soto-Ortega, Miguel; García-Báez, Efrén V

    2011-01-01

    In the title compound, C(31)H(38)O(17), the 1,3-dioxane and pyran-oside rings both show (4)C(1) chair conformations while for the d-fructofuran-oside moiety an envelop 3E conformation is observed. The phenyl ring is oriented almost perpendicular to the 1,3-dioxane ring [dihedral angle = 79.3 (2)°], and the acetate groups are equatorial for the pyran-oside ring and axial for the furan-oside ring. The analysis of potential hydrogen bonds shows both intra- and inter-molecular C-H⋯O contacts to be present. PMID:21523142

  13. Sources and potential health risk of gas phase PAHs in Hexi Corridor, Northwest China.

    PubMed

    Mao, Xiaoxuan; Yu, Zhousuo; Ding, Zhongyuan; Huang, Tao; Ma, Jianmin; Zhang, Gan; Li, Jun; Gao, Hong

    2016-02-01

    Gas phase polycyclic aromatic hydrocarbons (PAHs) in Hexi Corridor, Northwest China were determined during heating and non-heating seasons, respectively, using passive air samplers. Polyurethane foam (PUF) disks were chosen as the sampling medium. Fifteen PAHs out of the 16 PAHs classified by the United States Environmental Protection Agency (U.S. EPA) were detected in this field sampling investigation. The atmospheric levels of sampled PAHs were higher at urban sites than that at rural sites among 14 sampling sites and increased during heating season. The highest concentration (11.34 ng m(-3)) was observed in Lanzhou during the heating season, the capital and largest industrial city of Gansu Province. PAH contamination in air was dominated by three aromatic ring congeners. Possible sources of PAHs were apportioned using PAH species ratios and the principle component analysis (PCA) combined with a multiple linear regression (MLR) method. Fossil fuel consumption was identified to be the predominant source of PAHs over Hexi Corridor, accounting for 43 % of the concentration of total (15) PAHs. Backward and forward trajectory and cluster analysis were also carried out to identify potential origins of PAHs monitored at several urban and rural sites. Lung cancer risk of local residents to gas phase PAHs via inhalation exposure throughout the province was found to be around a critical value of the lung cancer risk level at 10(-6) recommended by the U.S. EPA risk assessment guideline. PMID:26432264

  14. Source identification of polycyclic aromatic hydrocarbons (PAHs) in sediment samples from the northern part of the Persian Gulf, Iran.

    PubMed

    Mirza, Roozbeh; Mohammadi, Mehdi; Faghiri, Iraj; Abedi, Ehsan; Fakhri, Ali; Azimi, Ali; Zahed, Mohammad Ali

    2014-11-01

    Samples of surface sediments from the Iranian coast of the Persian Gulf were examined to determine the levels and sources of 15 polycyclic aromatic hydrocarbons (PAHs). Samples were collected from 30 sampling sites and analyzed for PAHs by gas chromatography-mass spectrometry (GC-MS). Total concentrations of PAHs ranged from 93 to 4,077 ng g(-1) dry weight. The PAH composition from 30 sampling sites was dominated by four-ring PAH compounds. Molecular indices based on the ratios of PAH concentrations were used to differentiate PAHs from pyrolitic to petrogenic and mixed origins. The results suggested that the main sources of PAHs in sediments from the studied region were mixed pyrolitic and petrogenic. Furthermore, benthic organisms in most of the investigated areas were not at ecotoxicological risk, according to the results from the effects range low (ERL)/effects range median (ERM) techniques suggested by the US Sediment Quality Guidelines (SQGs). PMID:25023748

  15. Generation and distribution of PAHs in the process of medical waste incineration

    SciTech Connect

    Chen, Ying; Zhao, Rongzhi; Xue, Jun; Li, Jinhui

    2013-05-15

    Highlights: ► PAHs generation and distribution features of medical waste incineration are studied. ► More PAHs were found in fly ash than that in bottom ash. ► The highest proportion of PAHs consisted of the seven most carcinogenic ones. ► Increase of free oxygen molecule and burning temperature promote PAHs degradation. ► There is a moderate positive correlation between total PCDD/Fs and total PAHs. - Abstract: After the deadly earthquake on May 12, 2008 in Wenchuan county of China, several different incineration approaches were used for medical waste disposal. This paper investigates the generation properties of polycyclic aromatic hydrocarbons (PAHs) during the incineration. Samples were collected from the bottom ash in an open burning slash site, surface soil at the open burning site, bottom ash from a simple incinerator, bottom ash generated from the municipal solid waste (MSW) incinerator used for medical waste disposal, and bottom ash and fly ash from an incinerator exclusively used for medical waste. The species of PAHs were analyzed, and the toxicity equivalency quantities (TEQs) of samples calculated. Analysis results indicate that the content of total PAHs in fly ash was 1.8 × 10{sup 3} times higher than that in bottom ash, and that the strongly carcinogenic PAHs with four or more rings accumulated sensitively in fly ash. The test results of samples gathered from open burning site demonstrate that Acenaphthylene (ACY), Acenaphthene (ACE), Fluorene (FLU), Phenanthrene (PHE), Anthracene (ANT) and other PAHs were inclined to migrate into surrounding environment along air and surface watershed corridors, while 4- to 6-ring PAHs accumulated more likely in soil. Being consistent with other studies, it has also been confirmed that increases in both free oxygen molecules and combustion temperatures could promote the decomposition of polycyclic PAHs. In addition, without the influence of combustion conditions, there is a positive correlation between

  16. Characteristics of PAHs from deep-frying and frying cooking fumes.

    PubMed

    Yao, Zhiliang; Li, Jing; Wu, Bobo; Hao, Xuewei; Yin, Yong; Jiang, Xi

    2015-10-01

    Cooking fumes are an important indoor source of polycyclic aromatic hydrocarbons (PAHs). Because indoor pollution has a more substantial impact on human health than outdoor pollution, PAHs from cooking fumes have drawn considerable attention. In this study, 16 PAHs emitted through deep-frying and frying methods using rapeseed, soybean, peanut, and olive oil were examined under a laboratory fume hood. Controlled experiments were conducted to collect gas- and particulate-phase PAHs emitted from the cooking oil fumes, and PAH concentrations were quantified via high-performance liquid chromatography (HPLC). The results show that deep-frying methods generate more PAHs and benzo[a]pyrene (B[a]P) (1.3 and 10.9 times, respectively) because they consume greater volumes of edible oil and involve higher oil temperatures relative to those of frying methods. In addition, the total B[a]Peq concentration of deep-frying is 2.2-fold larger than that of frying. Regarding the four types of edible oils studied, rapeseed oil produced more PAH emission than the other three oil varieties. For all of the cooking tests, three- and four-ringed PAHs were the main PAH components regardless of the food and oil used. Concerning the PAH partition between gas and particulate phase, the gaseous compounds accounted for 59-96 % of the total. Meanwhile, the particulate fraction was richer of high molecular weight PAHs (five-six rings). Deep-frying and frying were confirmed as important sources of PAH pollution in internal environments. The results of this study provide additional insights into the polluting features of PAHs produced via cooking activities in indoor environments. PMID:26066859

  17. Distribution of polycyclic aromatic hydrocarbons (PAHs) in rivers and estuaries in Malaysia: a widespread input of petrogenic PAHs.

    PubMed

    Zakaria, Mohamad Pauzi; Takada, Hideshige; Tsutsumi, Shinobu; Ohno, Kei; Yamada, Junya; Kouno, Eriko; Kumata, Hidetoshi

    2002-05-01

    This is the first publication on the distribution and sources of polycyclic aromatic hydrocarbons (PAHs) in riverine and coastal sediments in South East Asia where the rapid transfer of land-based pollutants into aquatic environments by heavy rainfall and runoff waters is of great concern. Twenty-nine Malaysian riverine and coastal sediments were analyzed for PAHs (3-7 rings) by gas chromatography mass spectrometry. Total PAHs concentrations in the sediment ranged from 4 to 924 ng/g. Alkylated homologues were abundant for all sediment samples. The ratio of the sum of methylphenanthrenes to phenanthrene (MP/P), an index of petrogenic PAHs contribution, was more than unity for 26 sediment samples and more than 3 for seven samples for urban rivers covering a broad range of locations. The MP/P ratio showed a strong correlation with the total PAHs concentrations, with an r2 value of 0.74. This ratio and all other compositional features indicated that Malaysian urban sediments are heavily impacted by petrogenic PAHs. This finding is in contrast to other studies reported in many industrialized countries where PAHs are mostly of pyrogenic origin. The MP/P ratio was also significantly correlated with higher molecular weight PAHs such as benzo[a]pyrene, suggesting unique PAHs source in Malaysia which contains both petrogenic PAHs and pyrogenic PAHs. PAHs and hopanes fingerprints indicated that used crankcase oil is one of the major contributors of the sedimentary PAHs. Two major routes of inputs to aquatic environments have been identified: (1) spillage and dumping of waste crankcase oil and (2) leakage of crankcase oils from vehicles onto road surfaces, with the subsequent washout by street runoff. N-Cyclohexyl-2-benzothiazolamine (NCBA), a molecular marker of street dust, was detected in the polluted sediments. NCBA and other biomarker profiles confirmed our hypothesis of the input from street dust contained the leaked crankcase oil. The fingerprints excluded crude oil

  18. Polycyclic aromatic hydrocarbons (PAH) formation from the pyrolysis of different municipal solid waste fractions.

    PubMed

    Zhou, Hui; Wu, Chunfei; Onwudili, Jude A; Meng, Aihong; Zhang, Yanguo; Williams, Paul T

    2015-02-01

    The formation of 2-4 ring polycyclic aromatic hydrocarbons (PAH) from the pyrolysis of nine different municipal solid waste fractions (xylan, cellulose, lignin, pectin, starch, polyethylene (PE), polystyrene (PS), polyvinyl chloride (PVC), and polyethylene terephthalate (PET)) were investigated in a fixed bed furnace at 800 °C. The mass distribution of pyrolysis was also reported. The results showed that PS generated the most total PAH, followed by PVC, PET, and lignin. More PAH were detected from the pyrolysis of plastics than the pyrolysis of biomass. In the biomass group, lignin generated more PAH than others. Naphthalene was the most abundant PAH, and the amount of 1-methynaphthalene and 2-methynaphthalene was also notable. Phenanthrene and fluorene were the most abundant 3-ring PAH, while benzo[a]anthracene and chrysene were notable in the tar of PS, PVC, and PET. 2-ring PAH dominated all tar samples, and varied from 40 wt.% to 70 wt.%. For PS, PET and lignin, PAH may be generated directly from the aromatic structure of the feedstock. PMID:25312776

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

    PubMed

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

    2016-01-01

    There has been limited study of the removal of polycyclic aromatic hydrocarbons (PAHs) from inorganic clay minerals. Determining the amount of PAH removal is important in predicting their environmental fate. This study was carried out to the degradation and evaporation of PAHs from bentonite, which is an inorganic clay mineral. UV apparatus was designed specifically for the experiments. The impacts of temperature, UV, titanium dioxide (TiO2), and diethylamine (DEA) on PAH removal were determined. After 24 h, 75 and 44 % of ∑12 PAH in the bentonite were removed with and without UV rays, respectively. DEA was more effective as a photocatalyst than TiO2 during UV application. The ∑12 PAH removal ratio reached 88 % with the addition of DEA to the bentonite. It was concluded that PAHs were photodegraded at high ratios when the bentonite samples were exposed to UV radiation in the presence of a photocatalyst. At the end of all the PAH removal applications, higher evaporation ratios were obtained for 3-ring compounds than for heavier ones. More than 60 % of the amount of ∑12 PAH evaporated consisted of 3-ring compounds. PMID:26531715

  20. CRITICAL BODY RESIDUES FOR FRESHWATER AND SALTWATER AMPHIPODS EXPOSED TO SEDIMENT CONTAINING A MIXTURE OF HIGH KOW PAHS

    EPA Science Inventory

    Sediments were spiked with a mixture of 13 high log Kow (5.4-6.8) PAH compounds to determine critical body residues (CBR) in Hyalella azteca and Leptocheirus plumulosus. Hyalella were exposed for 28 d in a intermittent flow test and for 10 d in a static test to compare PAH uptake...

  1. Emission, distribution and toxicity of polycyclic aromatic hydrocarbons (PAHs) during municipal solid waste (MSW) and coal co-combustion.

    PubMed

    Peng, Nana; Li, Yi; Liu, Zhengang; Liu, Tingting; Gai, Chao

    2016-09-15

    Emission and distribution characteristics of polycyclic aromatic hydrocarbons (PAHs) were investigated during municipal solid waste (MSW) and coal combustion alone and MSW/coal blend (MSW weight fraction of 25%) co-combustion within a temperature range of 500°C-900°C. The results showed that for all combustion experiments, flue gas occupied the highest proportion of total PAHs and fly ash contained more high-ring PAHs. Moreover, the 3- and 4-ring PAHs accounted for the majority of total PAHs and Ant or Phe had the highest concentrations. Compared to coal, MSW combustion generated high levels of total PAHs with the range of 111.28μg/g-10,047.22μg/g and had high toxicity equivalent value (TEQ). MSW/coal co-combustion generated the smallest amounts of total PAHs and had the lowest TEQ than MSW and coal combustion alone. Significant synergistic interactions occurred between MSW and coal during co-combustion and the interactions suppressed the formation of PAHs, especially hazardous high-ring PAHs and decreased the TEQ. The present study indicated that the reduction of the yield and toxicity of PAHs can be achieved by co-combustion of MSW and coal. PMID:27265733

  2. Significance of Indirect Deposition on Wintertime PAH Concentrations in an Urban Northern California Creek

    PubMed Central

    Kim, Daekyun; Young, Thomas M.

    2009-01-01

    Abstract To investigate the main inputs and sources of polycyclic aromatic hydrocarbons (PAHs) into surface water, stream and precipitation samples were collected along an urban tributary to the Sacramento River, California. Dissolved, particulate, and colloid-bound PAHs were monitored four times between October 2004 and March 2005. The total PAH concentrations ranged from 192 to 3784 ng/L in surface water and from 77 to 236 ng/L in precipitation. Naphthalene, phenanthrene, pyrene, and benzo[g,h,i]perylene were the most abundant compounds in both rain and surface water. Surface water had truly dissolved PAH concentrations between 18 and 48 ng/L and precipitation had similar values (15–66 ng/L). PAHs larger than four rings were seldom found in the dissolved phase. Colloid-associated PAHs accounted for 4–25% of the total PAHs in rain, while they contributed only 0.1–6% to the total surface water PAHs. Indirect deposition (i.e., washoff of atmospheric particles previously deposited to land) 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 in California's Mediterranean climate. During the sampling period, there was not an obvious seasonal variation in dissolved PAH concentrations of surface water despite an enormous wintertime increase in the total aqueous concentrations. Particulate matter carried by stormwater runoff was the major source of PAHs in surface water in the early rainy season; this material likely represents a combination of indirect atmospheric inputs and other non-atmospheric anthropogenic inputs (e.g., oil leaks and spills). Selected PAH ratios indicate that observed PAHs in rainwater came from pyrogenic sources and those in surface water had more complicated and variable origins. PMID:20485462

  3. Ethanol-enhanced bioremediation of PAH-contaminated soils

    SciTech Connect

    Lee, P.H.; Ong, S.K.; Golchin, J.

    1999-07-01

    Bioremediation of soils contaminated with polycyclic aromatic hydrocarbons (PAHs) is highly challenging because of the low solubility and strong sorption properties of PAHs to soil organic matter. Two PAH-contaminated soils from former manufactured gas plant (MGP) sites were pretreated with ethanol to enhance the bioavailability of PAH compounds. The biodegradation of various PAHs in the pretreated soils was assessed using soil slurry reactor studies. The time needed to degrade 90% of the total PAH in the pretreated soils was at least 5 days faster than soils that were not pretreated with ethanol. A distinctive advantage with the pretreatment of soils with ethanol was the enhanced removal of 4-ring compounds such as chrysene. Approximately 90% of chrysene in the ethanol-treated soils were removed within 15 days while soils without pretreatment needed more than 30 days to obtain similar removal levels. After 35 days of biotreatment in the slurry reactors, approximately 40% of benzo(a)pyrene were removed in the ethanol-treated soils while only 20% were removed in soils not pretreated with ethanol.

  4. Biogeochemical Approaches to Assess PAH Pollution in an Urban Waterway.

    PubMed

    Cheng, Xianhao; Forsythe, Jennifer; Peterkin, Earl

    2015-12-01

    Biogeochemical approaches were applied to enhance the study on polycyclic aromatic hydrocarbon (PAH) pollution in an urban waterway. Chemical characterizations of PAHs in the studied area were identified, geochemical factors were revealed, and related mechanisms were discussed. It was found that, during summer, an early diagenetic process in the sediment could play a major role for the existence of high PAH concentrations, especially high molecular weight PAHs (≥ 4 rings), in the water column and sediment porewater. This effect could vary with tidal cycling, and higher PAH concentration in the water column would be expected during low tide. Other potential pollution sources were also evaluated in the studied creek. Results showed that pyrogenic sources dominated in the creek, generally. Nevertheless, petroleum products from a metal recycling plant could be an important point source to the waterway during wet weather. Comparing with previous studies in other waterways of the same watershed and published literature suggested that the limited toxicity to the ecosystem was only detected in sediments. More information needs to be collected during low tide for a more objective evaluation of PAH toxicity in the creek. PMID:26579786

  5. Biodegradation of Mixed PAHs by PAH-Degrading Endophytic Bacteria.

    PubMed

    Zhu, Xuezhu; Ni, Xue; Waigi, Michael Gatheru; Liu, Juan; Sun, Kai; Gao, Yanzheng

    2016-01-01

    Endophytic bacteria can promote plant growth, induce plant defence mechanisms, and increase plant resistance to organic contaminants. The aims of the present study were to isolate highly PAH-degrading endophytic bacteria from plants growing at PAH-contaminated sites and to evaluate the capabilities of these bacteria to degrade polycyclic aromatic hydrocarbons (PAHs) in vitro, which will be beneficial for re-colonizing target plants and reducing plant PAH residues through the inoculation of plants with endophytic bacteria. Two endophytic bacterial strains P₁ (Stenotrophomonas sp.) and P₃ (Pseudomonas sp.), which degraded more than 90% of phenanthrene (PHE) within 7 days, were isolated from Conyza canadensis and Trifolium pretense L., respectively. Both strains could use naphthalene (NAP), PHE, fluorene (FLR), pyrene (PYR), and benzo(a)pyrene (B(a)P) as the sole sources of carbon and energy. Moreover, these bacteria reduced the contamination of mixed PAHs at high levels after inoculation for 7 days; strain P₁ degraded 98.0% NAP, 83.1% FLR, 87.8% PHE, 14.4% PYR, and 1.6% B(a)P, and strain P₃ degraded 95.3% NAP, 87.9% FLR, 90.4% PHE, 6.9% PYR, and negligible B(a)P. Notably, the biodegradation of PAHs could be promoted through additional carbon and nitrogen nutrients; therein, beef extract was suggested as the optimal co-substrate for the degradation of PAHs by these two strains (99.1% PHE was degraded within 7 days). Compared with strain P₁, strain P₃ has more potential for the use in the removal of PAHs from plant tissues. These results provide a novel perspective in the reduction of plant PAH residues in PAH-contaminated sites through inoculating plants with highly PAH-degrading endophytic bacteria. PMID:27517944

  6. Biodegradation of Mixed PAHs by PAH-Degrading Endophytic Bacteria

    PubMed Central

    Zhu, Xuezhu; Ni, Xue; Waigi, Michael Gatheru; Liu, Juan; Sun, Kai; Gao, Yanzheng

    2016-01-01

    Endophytic bacteria can promote plant growth, induce plant defence mechanisms, and increase plant resistance to organic contaminants. The aims of the present study were to isolate highly PAH-degrading endophytic bacteria from plants growing at PAH-contaminated sites and to evaluate the capabilities of these bacteria to degrade polycyclic aromatic hydrocarbons (PAHs) in vitro, which will be beneficial for re-colonizing target plants and reducing plant PAH residues through the inoculation of plants with endophytic bacteria. Two endophytic bacterial strains P1 (Stenotrophomonas sp.) and P3 (Pseudomonas sp.), which degraded more than 90% of phenanthrene (PHE) within 7 days, were isolated from Conyza canadensis and Trifolium pretense L., respectively. Both strains could use naphthalene (NAP), PHE, fluorene (FLR), pyrene (PYR), and benzo(a)pyrene (B(a)P) as the sole sources of carbon and energy. Moreover, these bacteria reduced the contamination of mixed PAHs at high levels after inoculation for 7 days; strain P1 degraded 98.0% NAP, 83.1% FLR, 87.8% PHE, 14.4% PYR, and 1.6% B(a)P, and strain P3 degraded 95.3% NAP, 87.9% FLR, 90.4% PHE, 6.9% PYR, and negligible B(a)P. Notably, the biodegradation of PAHs could be promoted through additional carbon and nitrogen nutrients; therein, beef extract was suggested as the optimal co-substrate for the degradation of PAHs by these two strains (99.1% PHE was degraded within 7 days). Compared with strain P1, strain P3 has more potential for the use in the removal of PAHs from plant tissues. These results provide a novel perspective in the reduction of plant PAH residues in PAH-contaminated sites through inoculating plants with highly PAH-degrading endophytic bacteria. PMID:27517944

  7. Use of alternative growth substrates to enhance PAH degradation

    SciTech Connect

    Tittle, P.C.; Liu, Y.T.; Strand, S.E.; Stensel, H.D.

    1995-12-31

    Freshwater and saltwater polycyclic aromatic hydrocarbons (PAH)-degrading enrichments were developed from seed from a manufactured gas plant site and contaminated marine sediment, respectively. Both enrichments were able to maintain specific degradation rates of 3- and 4-ring PAHs after growth with salicylate or phthalate, which increased their biomass concentrations by a factor of 9 to 10. Phthalate was a more effective alternative substrate than was salicylate. Specific degradation rates of phenanthrene and anthracene by the freshwater enrichment were increased after growth with phthalate. Growth with phthalate increased the specific degradation rates of phenanthrene and pyrene by the saltwater enrichment.

  8. Occurrence, finger printing and ecological risk assessment of polycyclic aromatic hydrocarbons (PAHs) in the Chenab River, Pakistan.

    PubMed

    Farooq, Samiya; Eqani, Syed Ali-Musstjab-Akber-Shah; Malik, Riffat Naseem; Katsoyiannis, Athanasios; Zhang, Gan; Zhang, Yanlin; Li, Jun; Xiang, Liu; Jones, Kevin C; Shinwari, Zabta Khan

    2011-11-01

    Seventeen polycyclic aromatic hydrocarbons (PAHs) were studied in surface waters (including particulate phase) from the Chenab River, Pakistan and ranged from 289-994 and 437-1290 ng l(-1) in summer and winter (2007-09), respectively. Concentrations for different ring-number PAHs followed the trend: 3-rings > 2-rings > 4-rings > 5-rings > 6-rings. The possible sources of PAHs are identified by calculating the indicative ratios; appropriating petrogenic sources of PAHs in urban and sub-urban regions with pyrogenic sources in agricultural region. Factor analysis based on principal component analysis identified the origins of PAHs from industrial activities, coal and trash burning in agricultural areas and municipal waste disposal from surrounding urban and sub-urban areas via open drains into the riverine ecosystem. Water quality guidelines and toxic equivalent factors highlighted the potential risk of low molecular weight PAHs to the aquatic life of the Chenab River. The flux estimated for PAHs contaminants from the Chenab River to the Indus River was >50 tons/year. PMID:22006353

  9. Deuterated PAHs in Space

    NASA Technical Reports Server (NTRS)

    Peeters, Els; Allamandola, Louis J.; Bauschlicher, Charles W., Jr.; Hudgins, Douglas M.; Sandford, Scott A.; Tielens, A. G. G. M.; DeVincenzi, D. (Technical Monitor)

    2002-01-01

    The cosmic deuterium to hydrogen (D/H) ratio is of key importance from a cosmological and stellar evolution perspective since deuterium originates from big-bang nucleosynthesis and is destroyed by stellar thermonuclear reactions. Further, from the interstellar perspective, the galactic distribution of deuterium and the D/H ratio among various molecular species also traces interstellar chemical evolution. Over the past few decades, radio observations have enabled the study of a handful of small, deuterated interstellar species. However, the number of deuterated species detected and environments probed are limited, raising issues of selection effects that hamper generalization and applications to other environments. Infrared spectroscopy of the interstellar medium offers a distinct advantage in this regard as the extent of deuteration of entire chemical families, rather than one species, can be probed. These observations require spaceborne telescopes because the molecular vibrations involving D which produce the strongest IR bands fall in spectral regions which are obscured by terrestrial CO2 absorption. Here we report the tentative detection of the C-D stretching vibration from deuterated interstellar polycyclic aromatic hydrocarbons in the Orion nebula. Since the PAH emission features are widespread and probe many different types of cosmic environments, follow up observations of deuterated PAHs will provide fundamental, far reaching new insight and perspective into galactic and extragalactic processes.

  10. Using chemical desorption of PAHs from sediment to model biodegradation during bioavailability assessment.

    PubMed

    Spasojević, Jelena M; Maletić, Snežana P; Rončević, Srđan D; Radnović, Dragan V; Cučak, Dragana I; Tričković, Jelena S; Dalmacija, Božo D

    2015-01-01

    This work compares the biodegradation potential of four polycyclic aromatic hydrocarbons (PAH) (phenanthrene, pyrene, chrysene and benzo(a)pyrene, chosen as representatives of the 3, 4 and 5 ring PAHs) with their desorption from sediment by XAD4 resin and methyl-β-cyclodextrin (MCD). The biodegradation study was conducted under various conditions (biostimulation, bioaugmentation and their combination). The results show that total PAH removal in all treatments except biostimulation gave similar results, whereby the total amount of PAHs was decreased by about 30-35%. The desorption experiment showed that XAD4 desorbed a greater fraction of phenanthrene (77% versus 52%), and benzo(a)pyrene (44% versus 25%) than MCD. The results for four ring PAHs were similar for both desorption agents (about 30%). Comparing the maximum biodegraded amount of each PAH with the rapidly desorbed XAD4 and MCD fraction, XAD4 was found to correlate better with biodegradation for the high molecular PAHs (pyrene, chrysene, benzo(a)pyrene), although it overestimated the availability of phenanthrene. In contrast, MCD showed better correlation with the biodegradation of low molecular weight PAHs. PMID:25261761

  11. Sediment-porewater partitioning of polynuclear aromatic hydrocarbons (PAHs)

    SciTech Connect

    Maruya, K.A.; Risebrough, R.W.; Horne, A.J.

    1996-10-01

    Quantifying the distribution of hydrophobic organic compounds between contaminated sediment and interstitial water is key to understanding their fate and effects in aquatic ecosystems. Sampling during the wet and dry-seasons in San Francisco Bay has revealed that the extent of partitioning, measured as the apparent sediment organic carbon-porewater distribution coefficient (K{sub oc}{prime}), was positively correlated with the octanol-water distribution coefficient (K{sub ow}) for a suite of pyrogenically-derived, 2-6 ring PAHs. In addition, sediment PAHs (organic carbon basis) were associated with the silt fraction and organic carbon content. Moreover, K{sub oc}{prime} decreased along an intertidal gradient and was an order of magnitude higher during the wet season when runoff into the Bay was high. Our results provide evidence that substrate heterogeneity, a factor not accounted for in simple equilibrium models, can significantly alter the distribution of PAHs in this environment.

  12. Destruction of 2,4,6-trinitrotoluene by Fenton oxidation

    SciTech Connect

    Li, Z.M.; Comfort, S.D.; Shea, P.J.

    1997-03-01

    Past disposal practices at munitions production facilities have generated numerous acres of 2,4,6-trinitrotoluene (TNT)-contaminated soil. We determined the potential of the Fenton reagent (Fe{sup 2+} and H{sub 2}O{sub 2}) to remediate TNT contamination in water, aqueous extracts of contaminated soil, and soil-water slurries. The effects of H{sub 2}O{sub 2} and Fe{sup 2+} concentrations, solution pH, temperature, and initial TNT concentration on transformation and mineralization rates were evaluated. Treating an aqueous TNT solution (70 mg TNT L{sup -1}) with Fenton reagent (1% H{sub 2}O{sub 2}, 80 mg Fe{sup 2+} L{sup -1}) in the dark resulted in 100% destruction of TNT within 24 h. This coincided with 40% mineralization. Subsequent exposure to light resulted in >90% mineralization. We observed generation of 2,4,6-trinitrobenzoic acid and 1,3,5-trinitrobenzene within 15 min following Fenton oxidation of TNT. This indicates that initial TNT destruction likely occurs by methyl group oxidation and decarboxylation. Subsequent transformations involve nitro moiety removal with ring hydroxylation and cleavage, as evidenced by the stoichiometric recovery of TNT-nitrogen as NO{sub 3}{sup -} and production of oxalic acid as the primary C-containing end product. Upon exposure to light, Fe(II) was regenerated and the oxalate produced from 14C-TNT oxidation disappeared; this coincided with a decrease in solution {sup 14}C activity. Similar observations were made when {sup 14}C-oxalic acid was the starting substrate. Fenton oxidation was also effective in destroying TNT in aqueous extracts of contaminated soil and soil-water slurries. Experimental data provide evidence that the Fenton reagent can effectively remediate TNT-contaminated water and soil. 39 refs., 8 figs., 1 tab.

  13. Thermodynamic driving forces for PAH isomerization and growth during thermal treatment of polluted soils.

    PubMed

    Pope, C J; Peters, W A; Howard, J B

    2000-12-01

    For a limiting case of thermodynamic equilibrium, the importance of two classes of thermal chemical reactions that modify the structure and bioactivity of polycyclic aromatic hydrocarbons (PAH) was assessed computationally. These reactions are molecular weight (MW) growth by acetylene addition, and intramolecular rearrangement (isomerization). Temperatures (300-1100 degrees C), and the chemical environment (C(2)H(2)/H(2) molar ratios) were selected for relevancy to thermal treatment of PAH-contaminated soils under oxygen-free conditions. Molecular mechanics methods [MM3(92)] were used to compute thermochemical properties for calculation of equilibrium constants, i.e., heats of formation, standard entropies, and heat capacities for 30 PAH with empirical formulae C(14)H(10), C(16)H(10), C(18)H(10), C(18)H(12), C(20)H(10), and C(20)H(12). Included were 11 PAH containing only six-membered rings and 19 PAH containing both five- and six-membered rings. For each of these PAH the calculations predict that with increasing temperature, isomerization increases the "complexity" of the PAH mixture, i.e., the relative abundance of each PAH isomer in the mixture other than the most stable isomer, increases. Isomerization also partially transforms non-mutagens to mutagens, e.g., pyrene and benzo[e]pyrene to fluoranthene and benzo[a]pyrene, respectively, and partially converts cyclopenta[c, d]pyrene (CPEP) and chrysene, both human cell mutagens, to one and three additional human cell mutagens, respectively. Acetylene addition transforms the non-mutagens phenanthrene and pyrene to the mutagens triphenylene and CPEP, respectively. Some of the predicted PAH have been observed elsewhere among the products of aromatics pyrolysis. This study elucidates PAH reactivity for comparison with measurements, and identifies PAH reactions to be monitored and avoided in soil thermal decontamination and other waste remediation processes. PMID:11040395

  14. INTERACTION OF PAH-RELATED COMPOUNDS WITH THE ALPHA AND BETA ISOFORMS OF ESTROGEN RECEPTOR. (R826192)

    EPA Science Inventory

    The ability of several 4- and 5-ring polycyclic aromatic hydrocarbons (PAHs), heterocyclic PAHs, and their monohydroxy derivatives to interact with the estrogen receptor (ER) alpha and beta isoforms was examined. Only compounds possessing a hydroxyl group were able to compete wit...

  15. Phototransformation Rate Constants of PAHs Associated with Soot Particles

    PubMed Central

    Kim, Daekyun; Young, Thomas M.; Anastasio, Cort

    2013-01-01

    Photodegradation is a key process governing the residence time and fate of polycyclic aromatic hydrocarbons (PAHs) in particles, both in the atmosphere and after deposition. We have measured photodegradation rate constants of PAHs in bulk deposits of soot particles illuminated with simulated sunlight. The photodegradation rate constants at the surface (k0p), the effective diffusion coefficients (Deff), and the light penetration depths (z0.5) for PAHs on soot layers of variable thickness were determined by fitting experimental data with a model of coupled photolysis and diffusion. The overall disappearance rates of irradiated low molecular weight PAHs (with 2-3 rings) on soot particles were influenced by fast photodegradation and fast diffusion kinetics, while those of high molecular weight PAHs (with 4 or more rings) were apparently controlled by either the combination of slow photodegradation and slow diffusion kinetics or by very slow diffusion kinetics alone. The value of z0.5 is more sensitive to the soot layer thickness than the k0p value. As the thickness of the soot layer increases, the z0.5 values increase, but the k0p values are almost constant. The effective diffusion coefficients calculated from dark experiments are generally higher than those from the model fitting method for illumination experiments. Due to the correlation between k0p and z0.5 in thinner layers, Deff should be estimated by an independent method for better accuracy. Despite some limitations of the model used in this study, the fitted parameters were useful for describing empirical results of photodegradation of soot-associated PAHs. PMID:23247292

  16. Health risk assessment of inhabitants exposed to PAHs particulate matter in air.

    PubMed

    Froehner, Sandro; Maceno, Marcell; Machado, Karina Scurupa; Grube, Marianne

    2011-01-01

    The presence of polycyclic aromatic hydrocarbon compounds (PAHs) was investigated in the particulate matter of samples taken at six sampling sites in the city of Curitiba (southern Brazil). The concentrations of suspended particulate matter ranged from 11.02 to 177.27 ng/m(3). The analysis showed that 14 of the 16 PAHs are considered a priority compound by the USEPA (US Environmental Protection Agency). The mixture of PAHs was predominantly composed of PAHs with 3 and 4 aromatic rings. Isomer pair ratios show that the main source of PAHs was from burning fossil fuels (gasoline and diesel oil), although other sources may have contributed also. Benzo(a)pyrene, (BaP), regarded one of the most toxic PAHs, was present in all samples, but with concentrations lower than the maximum concentrations defined by some EU Countries. The risk assessment was conducted using the toxic equivalent factor (TEF) considering the toxicity of the individual PAHs compared to BaP. The BaP(eq) for all samples was between 0.42-1.12 ng/m(3). The equivalent BaP(eq) indicated low health risk associated with exposure to the total PAHs content in air. The incremental lifetime cancer risk (ILCR) model was used to find the risk level for workers close to the emitting pollution sources. Outdoor exposure showed no risk for the amount of PAHs emitted. The acceptable risk is 10(-6); however, all results were lower than this value. PMID:21644163

  17. Removing PAH`s with cells on fibers

    SciTech Connect

    Clyde, R.

    1996-12-31

    There are over 1,500 sites contaminated with polycyclic aromatic hydrocarbons from coal gas plants. White rot fungi degrade PAH`s in soil, but the problem is to supply oxygen needed for growth of the fungus. When old cardboard boxes are buried with the fungus, oxygen is entrapped in the corrugations. A method for growing the fungus quickly is also described. Pseudomonade also degrade PAH and several strains of this bacterium have been grown on fibers. The fibers have high area, and when Celite is entrapped in the fibers, more area is provided.

  18. Induction of PAH degradation in a phenanthrene-degrading pseudomonad

    SciTech Connect

    Stringfellow, W.T.; Chen, S.H.; Aitken, M.D.

    1995-12-31

    Recent evidence suggests that different polycyclic aromatic hydrocarbon (PAH) substrates are metabolized by common enzymes in PAH-degrading bacteria, implying that inducers for low-molecular-weight PAH degradation may coinduce for the metabolism of higher-molecular-weight compounds. The authors have tested this hypothesis with a well-characterized PAH-degrading bacterium, Pseudomonas saccharophila P-15. Growth of P-15 on salicylate, a metabolite of phenanthrene degradation, and a known inducer for naphthalene degradation, induced the metabolism of both substrates. Several potential inducers were then tested for their effects on metabolism of the four-ring compounds pyrene and fluoranthene, neither of which is a growth substrate for P-15, but both of which can be metabolized by this organism. Incubation of P-15 in the presence of phenanthrene or salicylate induced the metabolism of pyrene and fluoranthene in resting-cell assays. Catechol, another intermediate of naphthalene and phenanthrene degradation, did not induce the metabolism of either compound and interfered with the inducing effect of salicylate. These results have implications for strategies designed to maintain PAH degradation in contaminated environments, particularly for compounds that are degraded slowly or are degraded only by nongrowth metabolism.

  19. 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. PMID:25903173

  20. Alternative techniques to HPCD to evaluate the bioaccessible fraction of soil-associated PAHs and correlation to biodegradation efficiency.

    PubMed

    Crampon, M; Bodilis, J; Le Derf, F; Portet-Koltalo, F

    2016-08-15

    The total amount of polycyclic aromatic hydrocarbons (PAHs) in soils, given by exhaustive chemical extractions, does not relate directly to environmental risk, since only a fraction may be accessible to soil organisms. The rapid PAH desorbing fraction (Frap), which is weakly and reversibly sorbed to soils, is called the bioaccessible fraction, and can be estimated by non-exhaustive aqueous extractions. In order to better estimate Frap, different mild-extractants were tested, such as various cyclodextrins, surfactants and butanol. Their extractability performances were correlated to the Kd partition coefficients of seven PAHs obtained through sorption isotherms from five soils, but also to the PAHs molecular size and to the amounts of organic matter and of some clays (smectites and kaolinites). If hydroxypropyl-β-cyclodextrin was actually a good extractant to assess PAH accessibility, the polymer of carboxymethyl-β-cyclodextrin (pCMCD) was better (with a lower cost) to estimate the rapid mass transfer between soil particles and the soil solution, depending also on soil ageing. But Frap, estimated through pCMCD extractions, did not reflect the biodegradation of the PAHs after three months in soil microcosms. The chemical method underestimated the dissipation of 3-4 ring PAHs and overestimated that of 5-6 ring PAHs. So biodegradation was not only limited by PAHs mass-transfer, but also by biological factors, favoring the access of microorganisms to residual strongly sorbed fractions of 3-4 ring PAHs, and inhibiting the degradation of accessible but highly toxic 5-6 ring PAHs. PMID:27136727

  1. Change of PAHs with evolution of paddy soils from prehistoric to present over the last six millennia in the Yangtze River Delta region, China.

    PubMed

    Zhang, Jin; Cornelia, Mueller-Niggemann; Wang, Minyan; Cao, Zhihong; Luo, Xiping; Wong, Minghung; Chen, Wei

    2013-04-01

    To evaluate the influence of hydroponics management on soil organic components with evolution of paddy soil over the last six millennia, PAHs, as a biomarker, as well as total organic carbon content were used to explore changes of paddy soil organic carbon in two entirely buried ancient paddy soil profiles. The results showed that hydroponics management can cause organic carbon deposition in rice paddy. The changing of total PAH concentrations was not always in accordance with the changing of total organic carbon contents in layers of the buried ancient paddy soils. The PAHs in 6280 BP prehistoric paddy soil layer was 3-ring>5-ring>4-ring>6-ring, while in layers of the present paddy soil and the prehistoric upland were 3-ring>4-ring>5-ring>6-ring. The contribution of phenanthrene to total PAHs in two profiles and the increasing ratio of phenanthrene to alkylated PAHs from parent material/6280 BP prehistoric upland to 6280 BP paddy suggested substantial increase of the anthropogenic influence of hydroponics management on rice paddy soil. And in view of the (14)C age and bioremains in the two profiles, it was only possible for PAHs to be derived from hydroponics management with evolution of the paddy soils form the Neolithic age. Cadalene could be used as an indicator for biological sources of PAHs released by rice plant residues, and benzo[g,h,i]fluoranthene and benzo[g,h,i]perylene for pyrogenic sources released by field vegetation fires. PMID:23435064

  2. Partitioning of PAHs in pore water from mangrove wetlands in Shantou, China.

    PubMed

    Cao, Qi min; Wang, Hua; Qin, Jian qiao; Chen, Gui zhu; Zhang, Yong bei

    2015-01-01

    To investigate the trend of selected polycyclic aromatic hydrocarbons (PAHs) partitioning, fifteen pore water samples collected from the sediments of three mangrove wetlands were analyzed, and the partition coefficients and the partition model for the PAHs were determined by the correlation between K(oc) and octanol-water partition coefficient (K(ow)). The results revealed that the mean Kp values in inner mangrove wetlands were between 143 and 1031 L /Kg; the particulate organic carbon (POC) could strongly adsorb low-ring PAHs; the PAHs partitioning was on a obvious trend transported to particle phase. We suggest that the classic equilibrium model of organic carbon normalized (K(p)=K(oc)f(oc)) may be used to predict the trend of the selected PAHs partitioning. PMID:25450913

  3. Planetary Rings

    NASA Astrophysics Data System (ADS)

    Esposito, Larry

    2014-03-01

    Preface: a personal view of planetary rings; 1. Introduction: the allure of the ringed planets; 2. Studies of planetary rings 1610-2013; 3. Diversity of planetary rings; 4. Individual ring particles and their collisions; 5. Large-scale ring evolution; 6. Moons confine and sculpt rings; 7. Explaining ring phenomena; 8. N-body simulations; 9. Stochastic models; 10. Age and evolution of rings; 11. Saturn's mysterious F ring; 12. Uranus' rings and moons; 13. Neptune's partial rings; 14. Jupiter's ring-moon system after Galileo and New Horizons; 15. Ring photometry; 16. Dusty rings; 17. Concluding remarks; Afterword; Glossary; References; Index.

  4. Optimization of low ring polycylic aromatic biodegradation

    NASA Astrophysics Data System (ADS)

    Othman, N.; Abdul-Talib, S.; Tay, C. C.

    2016-07-01

    Polycyclic aromatic hydrocarbons (PAHs) are recalcitrance and persistence that finally turn into problematic environmental contaminants. Microbial degradation is considered to be the primary mechanism of PAHs removal from the environment due to its organic criteria. This study is carried out to optimize degradation process of low ring PAHs. Bacteria used in this study was isolated from sludge collected from Kolej Mawar, Universiti Teknologi MARA, Shah Alam, Selangor. Working condition namely, substrate concentration, bacteria concentration, pH and temperature were optimized. PAHs in the liquid sample was extracted by using solid phase microextractio equipped with a 7 µm polydimethylsiloxane (PDMS) SPME fibr. Removal of PAHs were assessed by measuring PAHs concentration using GC-FID. Results from the optimization study of biodegradation indicated that maximum rate of PAHs removal occurred at 100 mgL-1 of PAHs, 10% bacteria concentration, pH 7.0 and 30°C. These working condition had proved the effectiveness of using bacteria in biodegradation process of PAHs.

  5. Source apportionment of atmospheric PAHs and their toxicity using PMF: Impact of gas/particle partitioning

    NASA Astrophysics Data System (ADS)

    Gao, Bo; Wang, Xin-Ming; Zhao, Xiu-Ying; Ding, Xiang; Fu, Xiao-Xin; Zhang, Yan-Li; He, Quan-Fu; Zhang, Zhou; Liu, Teng-Yu; Huang, Zou-Zhao; Chen, Lai-Guo; Peng, Yan; Guo, Hai

    2015-02-01

    24-h PM2.5 samples were simultaneously collected at six sites in a subtropical city of South China during November-December, 2009. Particle-phase concentrations of polycyclic aromatic hydrocarbons (PAHs) and organic tracers such as hopanes for vehicular emissions (VE), levoglucosan for biomass burning (BB) and picene for coal combustion (CC) were determined. Meanwhile, their gas-phase concentrations were calculated from gas/particle (G/P) partitioning theory using the particle-phase concentrations. The 4 ring PAHs (fluoranthene to chrysene) had lower particle-phase fractions (10%-79%) than other species. Estimated BaPeq and lifetime cancer risk for particle-only (P-only) vs gas + particle (G + P) data sets showed similar values, indicating PAHs with 5-7 rings dominated the carcinogenicity of PAHs. Positive Matrix Factorization (PMF) was applied on both P-only and G + P data sets to estimate the source contributions to PAHs and their toxicity. Three common sources were identified: VE, BB and CC, with CC as the most significant source for both particulate (58%) and total (G + P, 40%) PAHs. While CC exhibited consistent contributions to BaPeq for P-only (66%) vs G + P (62%) solutions, VE and BB contributions were under- and overestimated by 68% and 47%, respectively by the P-only solution, as compared to the G + P solution. The results provide an insight on the impact of G/P partitioning on the source apportionment of PAHs and their toxicity.

  6. Laboratory Astrochemistry: Interstellar PAH Analogs

    NASA Technical Reports Server (NTRS)

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

    2000-01-01

    Polycyclic aromatic hydrocarbons (PAHs) are now considered to be an important and ubiquitous component of the organic material in space. PAHs are found in a large variety of extraterrestrial materials such as interplanetary dust particles (IDPs) and meteoritic materials. PAHs are also good candidates to account for the infrared emission bands (UIRs) and the diffuse interstellar optical absorption bands (DIBs) detected in various regions of the interstellar medium. The recent observations made with the Infrared Space Observatory (ISO) have confirmed the ubiquitous nature of the UIR bands and their carriers. PAHs are though to form through chemical reactions in the outflow from carbon-rich stars in a process similar to soot formation. Once injected in the interstellar medium, PAHs are further processed by the interstellar radiation field, interstellar shocks and energetic particles. A major, dedicated, laboratory effort has been undertaken over the past years to measure the physical and chemical characteristics of these complex molecules and their ions under experimental conditions that mimic the interstellar conditions. These measurements require collision-free conditions where the molecules and ions are cold and chemically isolated. The spectroscopy of PAHs under controlled conditions represents an essential diagnostic tool to study the evolution of extraterrestrial PAHs. The Astrochemistry Laboratory program will be discussed through its multiple aspects: objectives, approach and techniques adopted, adaptability to the nature of the problem(s), results and implications for astronomy as well as for molecular spectroscopy. A review of the data generated through laboratory simulations of space environments and the role these data have played in our current understanding of the properties of interstellar PAHs will be presented. The discussion will also introduce the newest generation of laboratory experiments that are currently being developed in order to provide a

  7. 11 CFR 4.6 - Discretionary release of exempt records.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 11 Federal Elections 1 2010-01-01 2010-01-01 false Discretionary release of exempt records. 4.6 Section 4.6 Federal Elections FEDERAL ELECTION COMMISSION PUBLIC RECORDS AND THE FREEDOM OF INFORMATION ACT § 4.6 Discretionary release of exempt records. The Commission may, in its discretion,...

  8. 16 CFR 4.6 - Cooperation with other agencies.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 16 Commercial Practices 1 2010-01-01 2010-01-01 false Cooperation with other agencies. 4.6 Section 4.6 Commercial Practices FEDERAL TRADE COMMISSION ORGANIZATION, PROCEDURES AND RULES OF PRACTICE MISCELLANEOUS RULES § 4.6 Cooperation with other agencies. It is the policy of the Commission to cooperate...

  9. 16 CFR 4.6 - Cooperation with other agencies.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 16 Commercial Practices 1 2012-01-01 2012-01-01 false Cooperation with other agencies. 4.6 Section 4.6 Commercial Practices FEDERAL TRADE COMMISSION ORGANIZATION, PROCEDURES AND RULES OF PRACTICE MISCELLANEOUS RULES § 4.6 Cooperation with other agencies. It is the policy of the Commission to cooperate...

  10. 16 CFR 4.6 - Cooperation with other agencies.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 16 Commercial Practices 1 2013-01-01 2013-01-01 false Cooperation with other agencies. 4.6 Section 4.6 Commercial Practices FEDERAL TRADE COMMISSION ORGANIZATION, PROCEDURES AND RULES OF PRACTICE MISCELLANEOUS RULES § 4.6 Cooperation with other agencies. It is the policy of the Commission to cooperate...

  11. 16 CFR 4.6 - Cooperation with other agencies.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 16 Commercial Practices 1 2014-01-01 2014-01-01 false Cooperation with other agencies. 4.6 Section 4.6 Commercial Practices FEDERAL TRADE COMMISSION ORGANIZATION, PROCEDURES AND RULES OF PRACTICE MISCELLANEOUS RULES § 4.6 Cooperation with other agencies. It is the policy of the Commission to cooperate...

  12. 16 CFR 4.6 - Cooperation with other agencies.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 16 Commercial Practices 1 2011-01-01 2011-01-01 false Cooperation with other agencies. 4.6 Section 4.6 Commercial Practices FEDERAL TRADE COMMISSION ORGANIZATION, PROCEDURES AND RULES OF PRACTICE MISCELLANEOUS RULES § 4.6 Cooperation with other agencies. It is the policy of the Commission to cooperate...

  13. 28 CFR 4.6 - Institution of proceedings.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 28 Judicial Administration 1 2010-07-01 2010-07-01 false Institution of proceedings. 4.6 Section 4.6 Judicial Administration DEPARTMENT OF JUSTICE PROCEDURE GOVERNING APPLICATIONS FOR CERTIFICATES OF... INCOME SECURITY ACT OF 1974 § 4.6 Institution of proceedings. All applications and supporting...

  14. 37 CFR 4.6 - Attorneys and Agents.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 37 Patents, Trademarks, and Copyrights 1 2011-07-01 2011-07-01 false Attorneys and Agents. 4.6 Section 4.6 Patents, Trademarks, and Copyrights UNITED STATES PATENT AND TRADEMARK OFFICE, DEPARTMENT OF COMMERCE GENERAL COMPLAINTS REGARDING INVENTION PROMOTERS § 4.6 Attorneys and Agents. Complaints...

  15. 37 CFR 4.6 - Attorneys and Agents.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 37 Patents, Trademarks, and Copyrights 1 2014-07-01 2014-07-01 false Attorneys and Agents. 4.6 Section 4.6 Patents, Trademarks, and Copyrights UNITED STATES PATENT AND TRADEMARK OFFICE, DEPARTMENT OF COMMERCE GENERAL COMPLAINTS REGARDING INVENTION PROMOTERS § 4.6 Attorneys and Agents. Complaints...

  16. 37 CFR 4.6 - Attorneys and Agents.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 37 Patents, Trademarks, and Copyrights 1 2013-07-01 2013-07-01 false Attorneys and Agents. 4.6 Section 4.6 Patents, Trademarks, and Copyrights UNITED STATES PATENT AND TRADEMARK OFFICE, DEPARTMENT OF COMMERCE GENERAL COMPLAINTS REGARDING INVENTION PROMOTERS § 4.6 Attorneys and Agents. Complaints...

  17. 37 CFR 4.6 - Attorneys and Agents.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 37 Patents, Trademarks, and Copyrights 1 2012-07-01 2012-07-01 false Attorneys and Agents. 4.6 Section 4.6 Patents, Trademarks, and Copyrights UNITED STATES PATENT AND TRADEMARK OFFICE, DEPARTMENT OF COMMERCE GENERAL COMPLAINTS REGARDING INVENTION PROMOTERS § 4.6 Attorneys and Agents. Complaints...

  18. 38 CFR 4.6 - Evaluation of evidence.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 38 Pensions, Bonuses, and Veterans' Relief 1 2010-07-01 2010-07-01 false Evaluation of evidence. 4.6 Section 4.6 Pensions, Bonuses, and Veterans' Relief DEPARTMENT OF VETERANS AFFAIRS SCHEDULE FOR RATING DISABILITIES General Policy in Rating § 4.6 Evaluation of evidence. The element of the weight to be accorded the character of the...

  19. Land treatment of PAH-contaminated soil: Performance measured by chemical and toxicity assays

    SciTech Connect

    Sayles, G.D.; Acheson, C.M.; Kupferle, M.J.; Shan, Y.; Zhou, Q.; Meier, J.R.; Chang, L.; Brenner, R.C.

    1999-12-01

    The performance of a soil remediation process can be determined by measuring the reduction in target soil contaminant concentrations and by assessing the treatment's ability to lower soil toxicity. Land treatment of polycyclic aromatic hydrocarbon (PAH)-contaminated soil from a former wood-treating site was simulated at pilot scale in temperature-controlled sol pans. Nineteen two- through six-ring PAHs were monitored with time (initial total PAHs = 2,800 mg/kg). Twenty-five weeks of treatment yielded a final total PAH level of 1,160 mg/kg. Statistically significant decreases in concentrations were seen in total, two-, three-, and four-ring PAHs. Carcinogenic and five- and six-ring PAHs showed no significant change in concentration. Land treatment resulted in significant toxicity reduction based on root elongation, Allium chromosomal aberration, and solid-phase Microtox bioassays. Acute toxicity, as measured by the earthworm survival assay, was significantly reduced and completely removed. The Ames spiral plate mutagenicity assay revealed that the untreated soil was slightly mutagenic and that treatment may have reduced mutagenicity. The variety of results generated from the chemical and toxicity assays emphasize the need for conducting a battery of such tests to fully understand soil remediation processes.

  20. Transducer influence of polycyclic aromatic hydrocarbons (PAHs) on photoisomerisation of 1-alkyl-2-(arylazo)imidazoles

    NASA Astrophysics Data System (ADS)

    Gayen, Pallab; Sinha, Chittaranjan

    2013-03-01

    The UV light irradiation to a solution of 1-alkyl-2-(arylazo)imidazole (L) in toluene shows transformation of trans to cis configuration about sbnd Ndbnd Nsbnd bond. The rate of photo-isomerisation and quantum yields are influenced by internal parameters like - nature of substituents, coordination to metal ions, steric and electronic effect, protonation etc. and the external factors like solvent (polarity, viscosity, dipole moment etc.), presence of innocent (to be chemically noninteracting) and noninnocent (chemically interacting) ions or molecules. In this work the influence of polycyclic aromatic hydrocarbons (PAH) such as - napththalene, anthracene, phenanthrene, pyrene - an innocent system, on the photochromic efficiency of L has been examined. The PAHs are π-donor and may form a π-π continuum with L which can significantly affect the motional (vibration, rotation) properties of the analyte and hence the photochromic activity. The rate and quantum yield of trans-to-cis isomerisation of L decrease with increasing [PAH] and also with increasing number of the fused phenyl ring(s) in PAH. Thus the photoisomerisation follows the rate sequence: no PAH > napththalene > anthracene-phenanthrene > pyrene. The reverse change, cis-to-trans is very slow upon light irradiation while appreciably fast in thermal process at dark. The activation energy (Ea) also decreases with [PAH] and number of fused phenyl rings.

  1. Microbial populations related to PAH biodegradation in an aged biostimulated creosote-contaminated soil.

    PubMed

    Lladó, Salvador; Jiménez, Nuria; Viñas, Marc; Solanas, Anna Maria

    2009-09-01

    A previous bioremediation survey on a creosote-contaminated soil showed that aeration and optimal humidity promoted depletion of three-ringed polycyclic aromatic hydrocarbons (PAHs), but residual concentrations of four-ringed benzo(a)anthracene (B(a)A) and chrysene (Chry) remained. In order to explain the lack of further degradation of heavier PAHs such as four-ringed PAHs and to analyze the microbial population responsible for PAH biodegradation, a chemical and microbial molecular approach was used. Using a slurry incubation strategy, soil in liquid mineral medium with and without additional B(a)A and Chry was found to contain a powerful PAH-degrading microbial community that eliminated 89% and 53% of the added B(a)A and Chry, respectively. It is hypothesized that the lack of PAH bioavailability hampered their further biodegradation in the unspiked soil. According to the results of the culture-dependent and independent techniques Mycobacterium parmense, Pseudomonas mexicana, and Sphingobacterials group could control B(a)A and Chry degradation in combination with several microorganisms with secondary metabolic activity. PMID:19153811

  2. Creating a full-sky map of PAH emission

    NASA Astrophysics Data System (ADS)

    Berkeley, Matthew; Kogut, Alan J.; Chuss, David T.; WISE

    2016-06-01

    Accurate characterization of foreground components has been a pressing issue in the CMB community for some time. In particular, the Anomalous Microwave Emission (AME), first detected in 1995 and confirmed by WMAP and Planck, has remained mysterious, though the leading hypothesis proposes that this excess emission is due to electric dipole emission from spinning dust grains. The leading candidate for such ‘spinning dust’ is Polycyclic Aromatic Hydrocarbons (PAHs). PAHs have characteristic emission lines in the mid-IR and can be analyzed using archived data from the WISE satellite. We have been working using publicly available data from WISE to create a full-sky map across the four WISE frequency bands: 3.4um, 4.6um, 12um and 22um. PAH emission is brightest in the 12um band; however it is possible to localize this population more accurately by linearly combining the maps across all four frequencies to create a full-sky map tracing the small-grain population of PAHs.We present preliminary results from this work.

  3. 4,6-Dihy-droxy-4,6-dimethyl-1,3-diazinane-2-thione.

    PubMed

    Aliyeva, Khatira N; Maharramov, Abel M; Allahverdiyev, Mirze A; Gurbanov, Atash V; Brito, Iván

    2011-09-01

    In the title compound, C(6)H(12)N(2)O(2)S, the heterocyclic ring has a sofa conformation. The mol-ecular conformation is stabilized by an intra-molecular O-H⋯O hydrogen-bond inter-action with graph-set motif S(6). In the crystal, mol-ecules are linked by O-H⋯S, N-H⋯S and N-H⋯O hydrogen-bond inter-actions, forming an extended two-dimensional framework parallel to the ac plane. PMID:22058933

  4. Distribution and partitioning of polycyclic aromatic hydrocarbons (PAHs) in different size fractions in sediments from Boston Harbor, United States.

    PubMed

    Wang, X C; Zhang, Y X; Chen, R F

    2001-11-01

    The concentrations of 16 US EPA priority pollutant polycyclic aromatic hydrocarbons (PAHs) were analyzed in four size fractions (< 62, 62-125, 125-250, and > 250 microm) in three contaminated Boston Harbor sediments. Total PAH concentrations ranged from 7.3 to 358 microg/g dry wt. and varied largely among the different size fractions in these sediments. For all three sites, the highest PAH concentrations were associated with the large size (> 250 microm) fractions while the fine silt and clay fractions (< 62 microm) contained relatively low PAHs. Despite the great concentration differences, the composition of PAHs in the four size fractions of these sediments showed similar patterns dominated by PAHs with three or more rings. By examining the distribution patterns of selected alkyl homologs to parent compounds, the results indicate that the major PAHs contributing to the high contamination in the inner harbor sediments were from pyrogenic sources. A positive correlation between PAHs and sedimentary organic carbon exists for all size fractions in the sediments. Calculated organic carbon normalized partition coefficients (log K(oc)) for selected major PAHs indicate near-equilibrium partitioning of PAHs among the different size fractions despite their large concentration variations. Sedimentary organic matter associated with different size fractions was the controlling factor for the observed distribution differences of PAHs among the size fractions. Our results also suggest that sedimentary organic matter with different origins and maturities may have somewhat different PAH sorption characteristics. Particulate organic matter of charcoal, plant detritus and Capitella fecal pellets in the sediments appear to sorb PAHs more strongly than organic matter associated with clay minerals. The strong association of PAHs with these organic particles in sediments will have a great influence not only on their distribution but also on long-term environmental impact. PMID:11763227

  5. Investigation of the release of PAHs from artificially contaminated sediments using cyclolipopeptidic biosurfactants.

    PubMed

    Portet-Koltalo, F; Ammami, M T; Benamar, A; Wang, H; Le Derf, F; Duclairoir-Poc, C

    2013-10-15

    Polycyclic aromatic hydrocarbons (PAHs) can be preponderant in contaminated sediments and understanding how they are sorbed in the different mineral and organic fractions of the sediment is critical for effective removal strategies. For this purpose, a mixture of seven PAHs was studied at the sediment/water interface and sorption isotherms were obtained. The influence of various factors on the sorption behavior of PAHs was evaluated, such as the nature of minerals, pH, ionic strength and amount of organic matter. Afterwards, the release of PAHs from the sediment by surfactants was investigated. The effectiveness of sodium dodecyl sulfate (SDS) was compared to natural biosurfactants, of cyclolipopeptidic type (amphisin and viscosin-like mixture), produced by two Pseudomonas fluorescens strains. The desorption of PAHs (from naphthalene to pyrene), from the highly retentive kaolinite fraction, could be favored by adding SDS or amphisin, but viscosin-like biosurfactants were only effective for 2-3 ring PAHs desorption (naphthalene to phenanthrene). Moreover, while SDS favors the release of all the target PAHs from a model sediment containing organic matter, the two biosurfactants tested were only effective to desorb the lowest molecular weight PAHs (naphthalene to fluorene). PMID:23995556

  6. Removal of polycyclic aromatic hydrocarbons (PAHs) from industrial sludges in the ambient air conditions: automotive industry.

    PubMed

    Karaca, Gizem; Tasdemir, Yucel

    2013-01-01

    Removal of polycyclic aromatic hydrocarbons (PAHs) existed in automotive industry treatment sludge was examined by considering the effects of temperature, UV, titanium dioxide (TiO2) and diethyl amine (DEA) in different dosages (i.e., 5% and 20%) in this study. Application of TiO2 and DEA to the sludge samples in ambient environment was studied. Ten PAH (Σ10 PAH) compounds were targeted and their average value in the sludge was found to be 4480 ± 1450 ng/g dry matter (DM). Total PAH content of the sludge was reduced by 25% in the ambient air environment. Meteorological conditions, atmospheric deposition, evaporation and sunlight irradiation played an effective role in the variations in PAH levels during the tests carried out in ambient air environment. Moreover, it was observed that when the ring numbers of PAHs increased, their removal rates also increased. Total PAH level did not change with the addition of 5% DEA and only 10% decreased with 5% TiO2 addition. PAH removal ratios were 8% and 32% when DEA (20%) and TiO2 (20%) were added, respectively. It was concluded that DEA was a weak photo-sensitizer yet TiO2 was effective only at 20% dosage. PMID:23485234

  7. Planetary Rings

    NASA Astrophysics Data System (ADS)

    Esposito, Larry W.

    2011-07-01

    Preface; 1. Introduction: the allure of ringed planets; 2. Studies of planetary rings 1610-2004; 3. Diversity of planetary rings; 4. Individual ring particles and their collisions; 5. Large-scale ring evolution; 6. Moons confine and sculpt rings; 7. Explaining ring phenomena; 8. N-Body simulations; 9. Stochastic models; 10. Age and evolution of rings; 11. Saturn's mysterious F ring; 12. Neptune's partial rings; 13. Jupiter's ring-moon system after Galileo; 14. Ring photometry; 15. Dusty rings; 16. Cassini observations; 17. Summary: the big questions; Glossary; References; Index.

  8. Characterization and source assessment of heavy metals and polycyclic aromatic hydrocarbons (PAHs) in sediments of the Fosu lagoon, Ghana

    SciTech Connect

    Gilbert, E.; Dodoo, D.K.; Okai-Sam, F.; Essuman, K.; Quagraine, E.K.

    2006-12-15

    The first results ever obtained on polycyclic aromatic hydrocarbon (PAHs) concentrations in the Fosu lagoon surface sediments are presented together with corresponding heavy metal (Fe, Mn, Cd, Zn and Ni) concentrations. Samples collected on a monthly basis from November 2003-April 2004 (heavy metals) and December 2003-January 2004 (PAHs) at 8 locations, representing different anthropogenic sources of contamination to the lagoon, were analyzed. Concentrations of Cd and Ni in the lagoon sediment suggest greater contamination to the lagoon from industrial activities in the vicinity of the lagoon; 50% of the sediment samples exceeded some established sediment Cd guidelines for the protection of aquatic lives. Then, 15 PAHs were detected among the sediments from the different locations and the compositional pattern in decreasing order was 3-ring {gt} 5-ring {gt} 4-ring {gt} 6-ring {gt} 2-ring PAH compounds. {Sigma} PAH concentrations in the sediment samples ranged from 254 to 558 mg/kg, with a mean of 359.4 mg/kg. Two distinct areas were identified to be a major source of anthropogenic load of both heavy metals and PAH; the mechanical shop in the northeastern sector of the lagoon is the main location for the input of Cd and it's associated PAH compounds (e.g., acenapthylene, acenaphthene, naphthalene and benzo(a)fluoranthene) and to a lesser extent Ni. Both combustion and petroleum sources may account for PAH loads from this area. The residential area in the northern sector is responsible for high loads of Mn and its associated PAH compounds (e.g., phenanthrene, benzo(a)pyrene and anthracene). These chemicals seem to enter the lagoon mainly by the combustion of especially wood or coal.

  9. Analysis of the Contribution of Individual Substituents in 4,6-Aminoglycoside-Ribosome Interaction

    PubMed Central

    Hobbie, Sven N.; Pfister, Peter; Brüll, Christian; Westhof, Eric; Böttger, Erik C.

    2005-01-01

    The 4,6-disubstituted 2-deoxystreptamines interfere with protein biosynthesis by specifically targeting the ribosomal A site. These drugs show subtle variations in the chemical groups of rings I, II, and III. In the present study we used site-directed mutagenesis to generate mutant strains of Mycobacterium smegmatis mc2155 SMR5 ΔrrnB with mutations in its single rRNA allele, rrnA. This genetic procedure gives rise to strains carrying homogeneous populations of mutant ribosomes and was used to study the contribution of individual chemical substituents to the binding of 4,6-disubstituted aminoglycosides. X-ray crystal structures of geneticin and tobramycin complexed to oligonucleotides containing the minimal bacterial ribosomal A site were used for interpretation of MICs determined for a panel of 4,6-aminoglycosides, including tobramycin, kanamycin A, kanamycin B, amikacin, gentamicin, and geneticin. Surprisingly, the considerable differences present within ring III did not seem to alter the interaction of the drug with the ribosome, as determined by site-directed mutagenesis of the A site. In contrast, subtle variations in ring I significantly influenced binding: (i) a 4′-hydroxyl moiety participates in the proper drug target interaction; and (ii) a 2′-amino group contributes an additional positive charge to ring I, making the drug less susceptible to any kind of sequence alteration within the decoding site, most notably, to conformational changes induced by transversion of U1495 to 1495A. The 4-amino-2-hydroxyl-1-oxobutyl extension at position 1 of ring II of amikacin provides an additional anchor and renders amikacin less dependent on the structural conformation of nucleotide U1406 compared to the dependencies of other kanamycins. Overall, the set of interactions forming the complex between drug substituents and nucleotides of the A site constitutes a network in which the interactions can partly compensate for each other when they are disrupted. PMID:16304180

  10. Polycyclic aromatic hydrocarbons (PAHs) in atmospheric PM2.5 around 2013 Asian Youth Games period in Nanjing

    NASA Astrophysics Data System (ADS)

    Li, Xuxu; Kong, Shaofei; Yin, Yan; Li, Li; Yuan, Liang; Li, Qi; Xiao, Hui; Chen, Kui

    2016-06-01

    Eighteen polycyclic aromatic hydrocarbons (PAHs) in PM2.5 collected near the Nanjing Olympic Sports Center across the Asian Youth Games (AYG) period (from August 2 to August 28, 2013) were analyzed using GC-MS. Their levels, sources and health risks to human were discussed. Results showed that the total concentrations of PAHs in PM2.5 were 9.43, 7.21 and 8.83 ng m- 3 for pre- (August 3-15), during- (August 16-24) and post- (August 25-28) AYG periods, respectively. They were dominated by 5-ring and 6-ring PAHs. Total PAHs concentrations in PM2.5 during AYG period decreased by 24%, when compared with those for pre-AYG period. For combustion-derived PAHs and carcinogenic PAHs, they decreased by 26% and 21%, respectively. It implied that the pollution control measures implemented during the AYG can effectively reduce the emission of PAHs from various sources. The poor correlations between PAHs and meteorological parameters also favored that the variations of PAHs were raised by the changes of emission sources. Diagnostic ratios and principal component analysis revealed that vehicle emission and coal combustion were the predominant contributors, with minimal effects from biomass burning and petroleum. The health risks for human exposed to PAHs in PM2.5 were quantitatively assessed by BaP equivalent concentration (BaPeq) and the incremental lifetime cancer risk (ILCR). The estimated ILCR value of PAHs during the AYG periods decreased by 23% and 27% for children and adults when compared with those for the pre-AYG, respectively. It indicated that the pollution control measures reduced the risks of PAHs to sportsmen or human gathered around the Olympic Sport Center.

  11. Polycyclic aromatic hydrocarbons (PAHs) concentration levels, pattern, source identification and soil toxicity assessment in urban traffic soil of Dhanbad, India.

    PubMed

    Suman, Swapnil; Sinha, Alok; Tarafdar, Abhrajyoti

    2016-03-01

    Present study was carried out to assess and understand potential health risk and to examine the impact of vehicular traffic on the contamination status of urban traffic soils in Dhanbad City with respect to polycyclic aromatic hydrocarbons (PAHs). Eight urban traffic sites and two control/rural site surface soils were analyzed and the contents of 13 priority PAHs was determined. Total PAH concentration at traffic sites ranged from 1.019 μg g(-1) to 10.856 μg g(-1) with an average value of 3.488 μg g(-1). At control/rural site, average concentration of total PAHs was found to be 0.640 μg g(-1). PAH pattern was dominated by four- and five-ring PAHs (contributing >50% to the total PAHs) at all the eight traffic sites. On the other hand, rural soil showed a predominance of low molecular weight three-ring PAHs (contributing >30% to the total PAHs). Indeno[123-cd]pyrene/benz[ghi]perylene (IP/BgP) ratio indicated that PAH load at the traffic sites is predominated by the gasoline-driven vehicles. The ratio of Ant/(Ant+Phe) varied from 0.03 to 0.44, averaging 0.10; Fla/(Fla+Pyr) from 0.39 to 0.954, averaging 0.52; BaA/(BaA+Chry) from 0.156 to 0.60, averaging 0.44; and IP/(IP+BgP) from 0.176 to 0.811, averaging 0.286. The results indicated that vehicular emission was the major source for PAHs contamination with moderate effect of coal combustion and biomass combustion. Carcinogenic potency of PAH load in traffic soil was nearly 6.15 times higher as compared to the control/rural soil. PMID:26747999

  12. PAH source fingerprints for coke ovens, diesel and, gasoline engines, highway tunnels, and wood combustion emissions

    NASA Astrophysics Data System (ADS)

    Khalili, Nasrin R.; Scheff, Peter A.; Holsen, Thomas M.

    To evaluate the chemical composition (source fingerprint) of the major sources of polyaromatic hydrocarbons (PAHs) in the Chicago metropolitan area, a study of major PAH sources was conducted during 1990-1992. In this study, a modified high-volume sampling method (PS-1 sampler) was employed to collect airborne PAHs in both the particulate and gas phases. Hewlett Packard 5890 gas chromatographs equipped with the flame ionization and mass spectrometer detectors (GC/FID and GC/MS) were used to analyze the samples. The sources sampled were: coke ovens, highway vehicles, heavy-duty diesel engines, gasoline engines and wood combustion. Results of this study showed that two and three ring PAHs were responsible for 98, 76, 92, 73 and 80% of the total concentration of measured 20 PAHs for coke ovens, diesel engines, highway tunnels, gasoline engines and wood combustion samples, respectively. Six ring PAHs such as indeno(1,2,3- cd)pyrene and benzo( ghi)perylene were mostly below the detection limit of this study and only detected in the highway tunnel, diesel and gasoline engine samples. The source fingerprints were obtained by averaging the ratios of individual PAH concentrations to the total concentration of categorical pollutants including: (a) total measured mass of PAHs with retention times between naphthalene and coronene, (b) the mass of the 20 PAHs measured in this study, (c) total VOCs, and (d) total PM10. Since concentrations of the above categorical pollutants were different for individual samples and different sources, the chemical composition patterns obtained for each categorical pollutant were different. The source fingerprints have been developed for use in chemical mass balance receptor modeling calculations.

  13. 5-(4-Hy-droxy-benzyl-idene)-2,2-dimethyl-1,3-dioxane-4,6-dione.

    PubMed

    Zeng, Wu-Lan

    2010-01-01

    The title compound, C(13)H(12)O(5), was prepared by the reaction of 2,2-dimethyl-1,3-dioxane-4,6-dione and 4-hy-droxy-benz-alde-hyde in ethanol. The 1,3-dioxane ring is in a distorted boat conformation. In the crystal, inversion dimers linked by pairs of O-H⋯O hydrogen bonds generate R(2) (2)(20) rings. PMID:21588666

  14. Petrology of types 4-6 carbonaceous chondrites

    NASA Technical Reports Server (NTRS)

    Scott, E. R. D.; Taylor, G. J.

    1985-01-01

    A comparative mineralogic study has been made of Coolidge, Karoonda, and new C4 chondrites in order to clarify the origin of C4-6 chondrites. It is shown that the properties of all C4-6 chondrites are consistent with an origin by metamorphism of C3-like precursors by processes analogous to those operating in ordinary chondrite parent bodies or planetesimals. However, type 4-6 material was not well mixed with type 3 material in the CV3 parent body. It is concluded that C4-6 chondrites may come from one or more separate parent bodies.

  15. A statistical approach to develop a detailed soot growth model using PAH characteristics

    SciTech Connect

    Raj, Abhijeet; Celnik, Matthew; Shirley, Raphael; Sander, Markus; Patterson, Robert; West, Richard; Kraft, Markus

    2009-04-15

    A detailed PAH growth model is developed, which is solved using a kinetic Monte Carlo algorithm. The model describes the structure and growth of planar PAH molecules, and is referred to as the kinetic Monte Carlo-aromatic site (KMC-ARS) model. A detailed PAH growth mechanism based on reactions at radical sites available in the literature, and additional reactions obtained from quantum chemistry calculations are used to model the PAH growth processes. New rates for the reactions involved in the cyclodehydrogenation process for the formation of 6-member rings on PAHs are calculated in this work based on density functional theory simulations. The KMC-ARS model is validated by comparing experimentally observed ensembles on PAHs with the computed ensembles for a C{sub 2}H{sub 2} and a C{sub 6}H{sub 6} flame at different heights above the burner. The motivation for this model is the development of a detailed soot particle population balance model which describes the evolution of an ensemble of soot particles based on their PAH structure. However, at present incorporating such a detailed model into a population balance is computationally unfeasible. Therefore, a simpler model referred to as the site-counting model has been developed, which replaces the structural information of the PAH molecules by their functional groups augmented with statistical closure expressions. This closure is obtained from the KMC-ARS model, which is used to develop correlations and statistics in different flame environments which describe such PAH structural information. These correlations and statistics are implemented in the site-counting model, and results from the site-counting model and the KMC-ARS model are in good agreement. Additionally the effect of steric hindrance in large PAH structures is investigated and correlations for sites unavailable for reaction are presented. (author)

  16. Characterization, identification of road dust PAHs in central Shanghai areas, China

    NASA Astrophysics Data System (ADS)

    Liu, M.; Cheng, S. B.; Ou, D. N.; Hou, L. J.; Gao, L.; Wang, L. L.; Xie, Y. S.; Yang, Y.; Xu, S. Y.

    Road dust samples were collected from central Shanghai in winter (January) and summer (August), respectively. Sixteen polycyclic aromatic hydrocarbons (PAHs) in the United States Environmental Protection Agency (USEPA) priority-controlled list were determined by GC/MS. Total PAH (t-PAH) concentrations in winter samples ranged from 9176 to 32,573 ng g -1 with a mean value of 20,648 ng g -1, while they varied from 6875 to 27,766 ng g -1 in summer with an average of 14,098 ng g -1. Spatial variation showed that city park (CP) samples had the lowest t-PAH concentration, while industrial area (ID) and traffic area (TR) and commercial area (CO) were the most polluted, in both seasons. PAH homologues concentrations were getting higher with the more rings and higher molecular weight (HMW) in all areas. The study of effective factors showed that grain size was only a minor factor influencing the accumulation of PAHs, whereas total organic carbon (TOC) was found to be closely correlated with t-PAH concentration. Prevailing winds could directly affect on the spatial distribution of PAHs. Chemical source apportionment studies took the form of principal component analysis (PCA), followed by compositional analysis. It was demonstrated that road dust PAHs in central Shanghai mainly came from the mixing of traffic and coal combustion. The contribution percentages of pyrogenic and petrogenic sources were respectively 71.0% and 11.4% in winter, while they were, 64.9% and 14.1% in summer, respectively. Road dust PAHs in Shanghai city mostly came from local sources.

  17. Impact of vehicular traffic emissions on particulate-bound PAHs: Levels and associated health risks

    NASA Astrophysics Data System (ADS)

    Slezakova, Klara; Castro, Dionísia; Delerue–Matos, Cristina; Alvim–Ferraz, Maria da Conceição; Morais, Simone; Pereira, Maria do Carmo

    2013-06-01

    Considering vehicular transport as one of the most health-relevant emission sources of urban air, and with aim to further understand its negative impact on human health, the objective of this work was to study its influence on levels of particulate-bound PAHs and to evaluate associated health risks. The 16 PAHs considered by USEPA as priority pollutants, and dibenzo[a,l]pyrene associated with fine (PM2.5) and coarse (PM2.5-10) particles were determined. The samples were collected at one urban site, as well as at a reference place for comparison. The results showed that the air of the urban site was more seriously polluted than at the reference one, with total concentrations of 17 PAHs being 2240% and 640% higher for PM2.5 and PM2.5-10, respectively; vehicular traffic was the major emission source at the urban site. PAHs were predominantly associated with PM2.5 (83% to 94% of ΣPAHs at urban and reference site, respectively) with 5 rings PAHs being the most abundant groups of compounds at both sites. The risks associated with exposure to particulate PAHs were evaluated using the TEF approach. The estimated value of lifetime lung cancer risks exceeded the health-based guideline levels, thus demonstrating that exposure to PM2.5-bound PAHs at levels found at urban site might cause potential health risks. Furthermore, the results showed that evaluation of benzo[a]pyrene (regarded as a marker of the genotoxic and carcinogenic PAHs) alone would probably underestimate the carcinogenic potential of the studied PAH mixtures.

  18. The source apportionment of polycyclic aromatic hydrocarbons (PAHs) in the topsoil in Xiaodian sewage irrigation area, North of China.

    PubMed

    Li, Jia-Le; Wang, Yan-Xin; Zhang, Cai-Xiang; Dong, Yi-Hui; Du, Bin; Liao, Xiao-Ping

    2014-12-01

    31 topsoil samples were collected by grid method in Xiaodian sewage irrigation area, Taiyuan City, North of China. The concentrations of 16 kinds of polycyclic aromatic hydrocarbons (PAHs) were determined by gas chromatograph coupled with mass spectrum. Generally speaking, the distribution order of PAHs in the area is: those with five and six rings > those with four rings > those with two and three rings. Source apportionment shows a significant zonation of the source of PAHs: the civil coal pollution occurred in the north part, the local and far factory pollution happened in the middle area and the mixed pollution sources from coal and wood combustion, automotive emission, presented in the south area. The distribution of PAHs has a definite relationship with the sewage water flow and soil adsorption. The related coefficient between PAHs and physicochemical property showed there was a negative correlation between pH, silt, clay and PAHs while there was a positive correlation between total organic carbon, sand and PAHs. PMID:25139034

  19. Electronically Excited States of Anisotropically Extended Singly-Deprotonated PAH Anions.

    PubMed

    Theis, Mallory L; Candian, Alessandra; Tielens, Alexander G G M; Lee, Timothy J; Fortenberry, Ryan C

    2015-12-31

    Polycyclic aromatic hydrocarbons (PAHs) play a significant role in the chemistry of the interstellar medium (ISM) as well as in hydrocarbon combustion. These molecules can have high levels of diversity with the inclusion of heteroatoms and the addition or removal of hydrogens to form charged or radical species. There is an abundance of data on the cationic forms of these molecules, but there have been many fewer studies on the anionic species. The present study focuses on the anionic forms of deprotonated PAHs. It has been shown in previous work that PAHs containing nitrogen heteroatoms (PANHs) have the ability to form valence excited states giving anions electronic absorption features. This work analyzes how the isoelectronic pure PAHs behave under similar structural constructions. Singly deprotonated forms of benzene, naphthalene, anthracene, and tetracene classes are examined. None of the neutral-radicals possess dipole moments large enough to support dipole-bound excited states in their corresponding closed-shell anions. Even though the PANH anion derivatives support valence excited states for three-ringed structures, it is not until four-ringed structures of the pure PAH anion derivatives that valence excited states are exhibited. However, anisotropically extended PAHs larger than tetracene will likely exhibit valence excited states. The relative energies for the anion isomers are very small for all of the systems in this study. PMID:26645382

  20. Predicting toxicity to Hyalella azteca in pyrogenic-impacted sediments-Do we need to analyze for all 34 PAHs?

    PubMed

    Geiger, Stephen C; Azzolina, Nicholas A; Nakles, David V; Hawthorne, Steven B

    2016-07-01

    Polycyclic aromatic hydrocarbons (PAHs) are major drivers of risk at many urban and/or industrialized sediment sites. The US Environmental Protection Agency (USEPA) currently recommends using measurements of 18 parent + 16 groups of alkylated PAHs (PAH-34) to assess the potential for sediment-bound PAHs to impact benthic organisms at these sites. ASTM Method D7363-13 was developed to directly measure low-level sediment porewater PAH concentrations. These concentrations are then compared to ambient water criteria (final chronic values [FCVs]) to assess the potential for impact to benthic organisms. The interlaboratory validation study that was used to finalize ASTM D7363-13 was developed using 24 of the 2-, 3-, and 4-ring PAHs (PAH-24) that are included in the USEPA PAH-34 analyte list. However, it is the responsibility of the user of ASTM Method D7363 to establish a test method to quantify the remaining 10 higher molecular weight PAHs that make up PAH-34. These higher molecular weight PAHs exhibit extremely low saturation solubilities that make their detection difficult in porewater, which has proven difficult to implement in a contract laboratory setting. As a result, commercial laboratories are hesitant to conduct the method on the entire PAH-34 analyte list. This article presents a statistical comparison of the ability of the PAH-24 and PAH-34 porewater results to predict survival of the freshwater amphipod Hyalella azteca, using the original 269 sediment samples used to gain ASTM D7363 Method approval. The statistical analysis shows that the PAH-24 are statistically indistinguishable from the PAH-34 for predicting toxicity. These results indicate that the analysis of freely dissolved porewater PAH-24 is sufficient for making risk-based decisions based on benthic invertebrate toxicity (survival and growth). This reduced target analyte list should result in a cost-saving for stakeholders and broader implementation of the method at PAH-impacted sediment sites

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

    NASA Astrophysics Data System (ADS)

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

    2009-12-01

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

  2. Toxicological profile for 2,4,6-trinitrotoluene

    SciTech Connect

    1995-11-01

    This Statement was prepared to give you information about 2,4,6-trinitrotoluene and to emphasize the human health effects that may result from exposure to it. The Environmental Protection Agency (EPA) has identified 1,397 sites on its National Priorities List (NPL). 2,4,6-Trinitrotoluene has been found in at least 20 of these sites.

  3. 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

  4. Transformation of PAHs during ethanol-Fenton treatment of an aged gasworks' soil.

    PubMed

    Lundstedt, Staffan; Persson, Ylva; Oberg, Lars

    2006-11-01

    PAH-contaminated soil from a former gasworks site was treated with Fenton's reagent in a number of lab-scale slurry reactors. The degradation result obtained by traditional Fenton oxidation and Fenton oxidation preceded by ethanol treatment were compared. The ethanol pre-treatment enhanced the depletion of all PAHs in the soil by facilitating their desorption from the soil matrix. However, some PAHs, especially anthracene, benzo[a]pyrene and perylene, were more extensively depleted than other PAHs with fewer or equal numbers of fused rings, indicating that the hydroxyl radicals react faster with these PAHs than with other kinds. The ethanol present in the slurry also appeared to influence the relative reactivity of the PAHs. Furthermore, the enhanced oxidation that occurred in the ethanol pre-treated soil resulted in the accumulation of oxidation products. For example, 1-indanone, anthracene-9,10-dione, 1-methylanthracenedione, 2-methylanthracenedione, 1,8-naphthalic anhydride, benz[a]anthracene-7,12-dione and two compounds tentatively identified as hydroxy-9-fluorenones were found at higher concentrations after the treatment than before it. The accumulation was most evident for the quinones, and in many cases it could be attributed to extensive oxidation of their parent PAHs, although the total oxidation efficiency in this study was relatively poor. PMID:16735053

  5. Aqueous accelerated solvent extraction of native polycyclic aromatic hydrocarbons (PAHs) from carbonaceous river floodplain soils.

    PubMed

    Yang, Yi; Hofmann, Thilo

    2009-10-01

    In this study, three river floodplain soils with different compositions of carbonaceous materials and a reference coal sample were extracted with water using the accelerated solvent extraction (ASE) method. The desorption enthalpy values for 2-ring PAHs were highest in the coal sample, with values in the soil samples decreasing with decrease in coal content. The values for the higher condensed PAHs showed that the highest desorption enthalpies were from the samples with the largest amount of coal-derived particles. Elevated desorption enthalpies indicated a strong bonding between PAHs and geosorbents. Moreover, with the application of ASE this study was able to conclude that the PAHs in the samples were preferentially adsorbed to carbonaceous materials with high surface areas. PMID:19524343

  6. Distribution, source apportionment, and transport of PAHs in sediments from the Pearl River Delta and the northern South China Sea

    SciTech Connect

    Luo, X.J.; Chen, S.J.; Mai, B.X.; Sheng, G.Y.; Fu, J.M.; Zeng, E.Y.

    2008-07-15

    Polycyclic aromatic hydrocarbons (PAHs) were measured in 59 surface sediments from rivers in the Pearl River Delta and the northern continental shelf of the South China Sea. Total PAH concentrations varied from 138 to 6,793 ng/g dry weight. The sources of PAH inputs to sediments in the Pearl River Delta were qualitatively and quantitatively determined by diagnostic ratios and principal components analysis with multiple linear regression. The results showed that on average coal and wood combustion, petroleum spills, vehicle emissions, and nature sources contributed 36%, 27%, 25%, and 12% of total PAHs, respectively. Coal and biomass combustion was the main source of PAHs in sediments of the South China Sea, whereas petroleum combustion was the main source of pyrolytic PAHs in riverine and estuarine sediments of the Pearl River Delta. Perylene was formed in situ in river sediments and then transported to coastal areas along with other PAHs. The relative abundance of perylene from five-ring PAHs can be used to estimate the contribution of riverine-discharged PAHs to coastal sediments.

  7. Polycyclic Aromatic Hydrocarbons (PAHs) in Indoor Dusts of Guizhou, Southwest of China: Status, Sources and Potential Human Health Risk

    PubMed Central

    Li, Baizhan

    2015-01-01

    Polycyclic aromatic hydrocarbons (PAHs) were analyzed for 136 indoor dust samples collected from Guizhou province, southwest of China. The ∑18PAHs concentrations ranged from 2.18 μg•g-1 to 14.20 μg•g-1 with the mean value of 6.78 μg•g-1. The highest Σ18PAHs concentration was found in dust samples from orefields, followed by city, town and village. Moreover, the mean concentration of Σ18PAHs in indoor dust was at least 10% higher than that of outdoors. The 4–6 rings PAHs, contributing more than 70% of ∑18PAHs, were the dominant species. PAHs ratios, principal component analysis with multiple linear regression (PCA-MLR) and hierarchical clustering analysis (HCA) were applied to evaluate the possible sources. Two major origins of PAHs in indoor dust were identified as vehicle emissions and coal combustion. The mean incremental lifetime cancer risk (ILCR) due to human exposure to indoor dust PAHs in city, town, village and orefield of Guizhou province, China was 6.14×10−6, 5.00×10−6, 3.08×10−6, 6.02×10−6 for children and 5.92×10−6, 4.83×10−6, 2.97×10−6, 5.81×10−6 for adults, respectively. PMID:25719362

  8. Levels, composition profiles and risk assessment of polycyclic aromatic hydrocarbons (PAHs) in sludge from ten textile dyeing plants.

    PubMed

    Ning, Xun-An; Lin, Mei-Qing; Shen, Ling-Zhi; Zhang, Jian-Hao; Wang, Jing-Yu; Wang, Yu-Jie; Yang, Zuo-Yi; Liu, Jing-Yong

    2014-07-01

    As components of synthetic dyes, polycyclic aromatic hydrocarbons (PAHs) are present as contaminants in textile dyeing sludge due to the recalcitrance in wastewater treatment process, which may pose a threat to environment in the process of sludge disposal. In order to evaluate PAHs in textile dyeing sludge, comprehensive investigation comprising 10 textile dyeing plants was undertaken. Levels, composition profiles and risk assessment of 16 EPA-priority PAHs were analyzed in this study. The total concentrations of 16 PAHs (∑16 PAHs) varied from 1463 ± 177 ng g(-1) to 16,714 ± 1,507 ng g(-1) with a mean value of 6386 ng g(-1). The composition profiles of PAHs were characterized by 3- and 4-ring PAHs, among which phenanthrene, anthracene and fluoranthene were the most dominant components. The mean benzo[a]pyrene equivalent (BaPeq) concentration of ∑16 PAHs in textile dyeing sludge was 423 ng g(-1), which was 2-3 times higher than concentrations reported for urban soil. According to ecological risk assessment, the levels of PAHs in the textile dyeing sludge may cause a significant risk to soil ecosystem after landfill or dumping on soil. PMID:24769559

  9. Microbial Factors Rather Than Bioavailability Limit the Rate and Extent of PAH Biodegradation in Aged Crude Oil Contaminated Model Soils

    SciTech Connect

    Huesemann, Michael H.; Hausmann, Tom S.; Fortman, Timothy J.

    2002-08-01

    The rate and extent of PAH biodegradation in a set of aged, crude oil contaminated model soils were measured in 90-week slurry bioremediation experiments. Soil properties such as organic matter content, mineral type, particle diameter, surface area, and porosity did not significantly influence the PAH biodegradation kinetics among the ten different model soils. A comparison of aged and freshly spiked soils indicates that aging affects the biodegradation rates and extents only for higher molecular weight PAHs while the effects of aging are insignificant for 3-ring PAHs and total PAHs. In all model soils with the exception of kaolinite clay, the rate of abiotic desorption was faster than the rate of biodegradation during the initial phase of bioremediation treatment indicating that PAH biodegradation was limited by microbial factors. Similarly, any of the higher molecular weight PAHs that were still present after 90 weeks of treatment were released rapidly during abiotic desorption tests which demonstrates that bioavailability limitations were not responsible for the recalcitrance of these hydrocarbons. Indeed, an analysis of microbial counts indicates that a severe reduction in hydrocarbon degrader populations may be responsible for the observed incomplete PAH biodegradation. It can therefore be concluded that the recalcitrance of PAHs during bioremediation is not necessarily due to bioavailability limitations and that these residual contaminants might, therefore, pose a greater risk to environmental receptors than previously thought.

  10. 5-(4-Fluoro-benzyl-idene)-2,2-dimethyl-1,3-dioxane-4,6-dione.

    PubMed

    Zeng, Wu-Lan

    2010-01-01

    The title compound, C(13)H(11)FO(4), was prepared by the reaction of 2,2-dimethyl-1,3-dioxane-4,6-dione and 4-fluoro-benz-alde-hyde in ethanol. The 1,3-dioxane ring adopts an envelope conformation. The crystal structure is stabilized by weak inter-molecular C-H⋯O hydrogen bonds. PMID:21588707

  11. 2,2-Dimethyl-5-[(pyridin-2-yl-amino)-methyl-idene]-1,3-dioxane-4,6-dione.

    PubMed

    Shi, Jian-You; Li, Jin-Qi; Tong, Rong-Sheng; Lin, He; Lu, Chen

    2011-01-01

    In the title compound, C(12)H(12)N(2)O(4), the dihedral angle between the pyridine and enamine planes is 3.5 (3)°, while the angle between the dioxanedione (seven atoms) and enamine planes is 4.6 (3)°. The dioxane ring approximates an envelope conformation. PMID:21522947

  12. Generation and distribution of PAHs in the process of medical waste incineration.

    PubMed

    Chen, Ying; Zhao, Rongzhi; Xue, Jun; Li, Jinhui

    2013-05-01

    After the deadly earthquake on May 12, 2008 in Wenchuan county of China, several different incineration approaches were used for medical waste disposal. This paper investigates the generation properties of polycyclic aromatic hydrocarbons (PAHs) during the incineration. Samples were collected from the bottom ash in an open burning slash site, surface soil at the open burning site, bottom ash from a simple incinerator, bottom ash generated from the municipal solid waste (MSW) incinerator used for medical waste disposal, and bottom ash and fly ash from an incinerator exclusively used for medical waste. The species of PAHs were analyzed, and the toxicity equivalency quantities (TEQs) of samples calculated. Analysis results indicate that the content of total PAHs in fly ash was 1.8×10(3) times higher than that in bottom ash, and that the strongly carcinogenic PAHs with four or more rings accumulated sensitively in fly ash. The test results of samples gathered from open burning site demonstrate that Acenaphthylene (ACY), Acenaphthene (ACE), Fluorene (FLU), Phenanthrene (PHE), Anthracene (ANT) and other PAHs were inclined to migrate into surrounding environment along air and surface watershed corridors, while 4- to 6-ring PAHs accumulated more likely in soil. Being consistent with other studies, it has also been confirmed that increases in both free oxygen molecules and combustion temperatures could promote the decomposition of polycyclic PAHs. In addition, without the influence of combustion conditions, there is a positive correlation between total PCDD/Fs and total PAHs, although no such relationship has been found for TEQ. PMID:23462270

  13. Biodegradation of PAHs in Soil: Influence of Initial PAHs Concentration

    NASA Astrophysics Data System (ADS)

    Kamil, N. A. F. M.; Talib, S. A.

    2016-07-01

    Most studies on biodegradation of Polycyclic Aromatic Hydrocarbons (PAHs) evaluate the effect of initial PAHs concentration in liquid medium. There are limited studies on evaluation in solid medium such as contaminated soil. This study investigated the potential of the bacteria, Corynebacterium urealyticum isolated from municipal sludge in degrading phenanthrene contaminated soil in different phenanthrene concentration. Batch experiments were conducted over 20 days in reactors containing artificially contaminated phenanthrene soil at different concentration inoculated with a bacterial culture. This study established the optimum condition for phenanthrene degradation by the bacteria under nonindigenous condition at 500 mg/kg of initial phenanthrene concentration. High initial concentration required longer duration for biodegradation process compared to low initial concentration. The bacteria can survive for three days for all initial phenanthrene concentrations.

  14. Biodegradation of PAH`s in sediment-slurry processes

    SciTech Connect

    Hughes, J.B.; Beckles, D.; Chandra, S.

    1995-12-31

    The focus of this research was to examine biodegradation of polynuclear aromatic hydrocarbons (PAHs) in lab scale slurry reactors. The studies summarized in this paper focused on the rate and extent of contaminant release from the sediments, oxygen demand of anaerobic sediments, and the rate and extent of PAH biodegradation achieved. Mass balances were used in all cases. The studies identified several factors which may influence the design or operation of bioreactors used for sediment remediation. Mixing had the greatest effect on the rate and extent of contaminant release; solids loading and aeration had little or no effect in mixed reactors. In unmixed reactors, aerated systems showed faster rates of contaminant release than unaerated systems, indicating that the aeration process itself provides some degree of mixing. The maximum extent of mineralization appeared to be reached within five days in mixed systems; significantly lower mineralization was seen in reactors with insufficient mixing.

  15. Spatial-temporal trend and health implications of polycyclic aromatic hydrocarbons (PAHs) in resident oysters, South China Sea: A case study of Eastern Guangdong coast.

    PubMed

    Yu, Zi-Ling; Lin, Qin; Gu, Yang-Guang; Ke, Chang-Liang; Sun, Run-Xia

    2016-09-15

    Spatial and temporal distributions of polycyclic aromatic hydrocarbons (PAHs) were investigated in Eastern Guangdong coast, China. Total PAH concentrations in oysters ranged from 231 to 1178ng/g with a mean concentration of 622ng/g dry weight. Compared with other bays and estuaries, PAH levels in oysters were moderate. Spatial distribution of PAHs was site specific, with relatively high PAH concentrations observed in Zhelin Bay and Kaozhouyang Bay. Based on the Spearman test analysis, only PAH concentration in oysters from Jiazi Harbor showed a significant increasing trend (P<0.05). Three-ring PAHs were the most abundant, accounting for 54.2%-88.4% of total PAHs. Diagnostic ratios suggested that PAHs were derived mainly from petroleum origin. BaP and ∑4PAH concentrations were well within the European Union limits (5ng/g and 30ng/g wet weight, respectively). The incremental lifetime cancer risks (ILCR) for PAHs were <10(-5), indicating that the adverse health risks associated with oyster consumption in this area were minimal. PMID:27345707

  16. Desorption and Bioavailability of PAHs in Contaminated Soil Subjected to Long-Term In Situ Biostimulation

    PubMed Central

    Richardson, Stephen D.; Aitken, Michael D.

    2011-01-01

    The distribution and potential bioavailability of polycyclic aromatic hydrocarbons (PAHs) in soil from a former manufactured-gas plant (MGP) site were examined before and after long-term biostimulation under simulated in situ conditions. Treated soil was collected from the oxygenated zones of two continuous-flow columns, one subjected to biostimulation and the other serving as a control, and separated into low- and high-density fractions. In the original soil, over 50% of the total PAH mass was associated with lower-density particles, which comprised < 2% of the total soil mass. However, desorbable fractions of PAHs were much lower in the low-density material than in the high-density material. After over 500 d of biostimulation, significant removal of total PAHs occurred in both the high- and low-density materials (77% and 53%, respectively), with three- and four-ring PAHs accounting for the majority of the observed mass loss. Total PAHs that desorbed over a 28-d period were substantially lower in treated soil from the biostimulated column than in the original soil for both the high-density material (23 versus 63%) and low-density material (5 versus 20%). The fast-desorbing fractions quantified by a two-site desorption model ranged from 0.1 to 0.5 for most PAHs in the original soil but were essentially zero in the biostimulated soil. The fast-desorbing fractions in the original soil underestimated the extent of PAH biodegradation observed in the biostimulated column, and thus was not a good predictor of PAH bioavailability after long-term, simulated in situ biostimulation. PMID:21932296

  17. Targeting CDK4/6 in patients with cancer.

    PubMed

    Hamilton, Erika; Infante, Jeffrey R

    2016-04-01

    The cyclin D-cyclin dependent kinase (CDK) 4/6-inhibitor of CDK4 (INK4)-retinoblastoma (Rb) pathway controls cell cycle progression by regulating the G1-S checkpoint. Dysregulation of the cyclin D-CDK4/6-INK4-Rb pathway results in increased proliferation, and is frequently observed in many types of cancer. Pathway activation can occur through a variety of mechanisms, including gene amplification or rearrangement, loss of negative regulators, epigenetic alterations, and point mutations in key pathway components. Due to the importance of CDK4/6 activity in cancer cells, CDK4/6 inhibitors have emerged as promising candidates for cancer treatment. Moreover, combination of a CDK4/6 inhibitor with other targeted therapies may help overcome acquired or de novo treatment resistance. Ongoing studies include combinations of CDK4/6 inhibitors with endocrine therapy and phosphatidylinositol 3-kinase (PI3K) pathway inhibitors for hormone receptor-positive (HR+) breast cancers, and with selective RAF and MEK inhibitors for tumors with alterations in the mitogen activated protein kinase (MAPK) pathway such as melanoma. In particular, the combination of CDK4/6 inhibitors with endocrine therapy, such as palbociclib's recent first-line approval in combination with letrozole, is expected to transform the treatment of HR+ breast cancer. Currently, three selective CDK4/6 inhibitors have been approved or are in late-stage development: palbociclib (PD-0332991), ribociclib (LEE011), and abemaciclib (LY2835219). Here we describe the current preclinical and clinical data for these novel agents and discuss combination strategies with other agents for the treatment of cancer. PMID:27017286

  18. Treating cancer with selective CDK4/6 inhibitors.

    PubMed

    O'Leary, Ben; Finn, Richard S; Turner, Nicholas C

    2016-07-01

    Uncontrolled cellular proliferation, mediated by dysregulation of the cell-cycle machinery and activation of cyclin-dependent kinases (CDKs) to promote cell-cycle progression, lies at the heart of cancer as a pathological process. Clinical implementation of first-generation, nonselective CDK inhibitors, designed to inhibit this proliferation, was originally hampered by the high risk of toxicity and lack of efficacy noted with these agents. The emergence of a new generation of selective CDK4/6 inhibitors, including ribociclib, abemaciclib and palbociclib, has enabled tumour types in which CDK4/6 has a pivotal role in the G1-to-S-phase cell-cycle transition to be targeted with improved effectiveness, and fewer adverse effects. Results of pivotal phase III trials investigating palbociclib in patients with advanced-stage oestrogen receptor (ER)-positive breast cancer have demonstrated a substantial improvement in progression-free survival, with a well-tolerated toxicity profile. Mechanisms of acquired resistance to CDK4/6 inhibitors are beginning to emerge that, although unwelcome, might enable rational post-CDK4/6 inhibitor therapeutic strategies to be identified. Extending the use of CDK4/6 inhibitors beyond ER-positive breast cancer is challenging, and will likely require biomarkers that are predictive of a response, and the use of combination therapies in order to optimize CDK4/6 targeting. PMID:27030077

  19. A PI 4. 6 peroxidase that specifically crosslinks extensin precursors

    SciTech Connect

    Upham, B.L; Alizadeh, H.; Ryan, K.J.; Lamport, D.T.A. )

    1991-05-01

    The primary cell wall is a microcomposite of cellulose, pectin, hemicellulose and protein. The warp-weft model of the primary cell wall hypothesize that extensin monomers are intermolecularly crosslinked orthogonal to the cellulose microfibril thus mechanically coupling the major load-bearing polymer: cellulose. Media of tomato cell cultures contains heat labile, peroxide dependent crosslinking activity, as determined by the rate of decrease in monomer concentration analyzed via Superose-6. Isoelectric focusing of tomato cell culture media indicated crosslinking was predominantly in the acidic peroxidase fraction (pI4.6). This peroxidase was partially purified by ultracentrifugation, DEAE-Trisacryl and HPLC-DEAE chromatography techniques resulting in a 90 fold purification and 45% yield. A second acidic peroxidase eluted from the HPLC-DEAE column had 25% of the crosslinking activity of the pI 4.6 peroxidase. Purified basic peroxidase had only 0.7% of the activity of the pI 4.6 peroxidase. The specific activity of the pI 4.6 peroxidase was 5,473 mg extensin crosslinked/min/mg peroxidase. The pI 4.6 peroxidase crosslinked the following extensins: tomato I and II, carrot, Ginkgo II and did not crosslink Ginkgo I, Douglas Fir, Maize, Asparagus I and II, and sugarbeet extensins as well as bovine serum albumin. Comparison of motifs common to extensins that are crosslinked by the pI 4.6 peroxidase may help identify the crosslink domain(s) of extension.

  20. Influence of vegetation on the in situ bacterial community and polycyclic aromatic hydrocarbon (PAH) degraders in aged PAH-contaminated or thermal-desorption-treated soil.

    PubMed

    Cébron, Aurélie; Beguiristain, Thierry; Faure, Pierre; Norini, Marie-Paule; Masfaraud, Jean-François; Leyval, Corinne

    2009-10-01

    ) and gram-positive (GP) PAH-degrading bacteria was estimated by real-time PCR quantification of specific functional genes encoding the alpha subunit of PAH-ring hydroxylating dioxygenase (PAH-RHD(alpha)). The percentage of the PAH-RHD(alpha) GN bacterial genes relative to 16S rRNA gene density decreased with time in all the plots. The GP PAH-RHD(alpha) bacterial gene proportion decreased in the NM-BS plots but stayed constant or increased under vegetation influence (NM-SV, NM-Ms, and TD-Ms). PMID:19633127

  1. Influence of Vegetation on the In Situ Bacterial Community and Polycyclic Aromatic Hydrocarbon (PAH) Degraders in Aged PAH-Contaminated or Thermal-Desorption-Treated Soil▿ †

    PubMed Central

    Cébron, Aurélie; Beguiristain, Thierry; Faure, Pierre; Norini, Marie-Paule; Masfaraud, Jean-François; Leyval, Corinne

    2009-01-01

    ) and gram-positive (GP) PAH-degrading bacteria was estimated by real-time PCR quantification of specific functional genes encoding the α subunit of PAH-ring hydroxylating dioxygenase (PAH-RHDα). The percentage of the PAH-RHDα GN bacterial genes relative to 16S rRNA gene density decreased with time in all the plots. The GP PAH-RHDα bacterial gene proportion decreased in the NM-BS plots but stayed constant or increased under vegetation influence (NM-SV, NM-Ms, and TD-Ms). PMID:19633127

  2. Planetary rings

    SciTech Connect

    Greenberg, R.; Brahic, A.

    1984-01-01

    Among the topics discussed are the development history of planetary ring research, the view of planetary rings in astronomy and cosmology over the period 1600-1900, the characteristics of the ring systems of Saturn and Uranus, the ethereal rings of Jupiter and Saturn, dust-magnetosphere interactions, the effects of radiation forces on dust particles, the collisional interactions and physical nature of ring particles, transport effects due to particle erosion mechanisms, and collision-induced transport processes in planetary rings. Also discussed are planetary ring waves, ring particle dynamics in resonances, the dynamics of narrow rings, the origin and evolution of planetary rings, the solar nebula and planetary disk, future studies of the planetary rings by space probes, ground-based observatories and earth-orbiting satellites, and unsolved problems in planetary ring dynamics.

  3. PAH Emission at the Bright Locations of PDRs: the grandPAH Hypothesis

    NASA Astrophysics Data System (ADS)

    Andrews, H.; Boersma, C.; Werner, M. W.; Livingston, J.; Allamandola, L. J.; Tielens, A. G. G. M.

    2015-07-01

    The polycyclic aromatic hydrocarbon (PAH) emission observed in the Spitzer Infrared Spectrograph spectra of bright mid-IR locations of NGC 7023, NGC 2023, and NGC 1333 was analyzed. These objects show large variations in PAH band ratios when studied through spectral mapping. Nevertheless, the mid-IR spectra at these bright spots show a remarkably similar PAH emission. We used the NASA Ames PAH IR Spectroscopic Database to fit the observations and analyze the derived PAH populations. Our results show that PAH emission in the 5-15 μm range appears to be rather insensitive to variations of the radiation field. Similar PAH populations of neutral small to medium-sized PAHs (˜50%), with ionized species contributing in slightly less than 50%, provide very good fits. Analyzing the degeneracy of the results shows that subtle (but intrinsic) variations in the emission properties of individual PAHs lead to observable differences in the resulting spectra. On top of this, we found that variations of <30% in the PAH abundances would lead to noticeable spectral differences between the three photodissociation regions (PDRs). Therefore, PAH populations must be remarkably similar at these different lines of sight. To account for this, we suggest the concept of grandPAHs as a unique mixture of the most stable PAHs emitting at these spots. Using NGC 7023 as an example, the grandPAHs refer to the robust PAH population that results from the intense processing of PAHs at the border limit between the PDR and the molecular cloud, where, due to the UV radiation that destroys the PAH population, the abundance of PAHs starts decreasing as we move toward the star.

  4. The hydrogen coverage of interstellar PAHs

    NASA Technical Reports Server (NTRS)

    Barker, J. R.; Cohen, M.; Tielens, Alexander G. G. M.; Allamandola, Louis J.; Barker, J. R.; Barker, J. R.

    1986-01-01

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

  5. The hydrogen coverage of interstellar PAHs

    NASA Technical Reports Server (NTRS)

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

    1987-01-01

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

  6. Polycyclic aromatic hydrocarbons (PAHs) in sediments of Zhelin Bay, the largest mariculture base on the eastern Guangdong coast, South China: Characterization and risk implications.

    PubMed

    Gu, Yang-Guang; Ke, Chang-Liang; Liu, Qi; Lin, Qin

    2016-09-15

    We investigated distribution, sources, and potential risks of polycyclic aromatic hydrocarbons (PAHs) in the surface sediments from the largest mariculture base in the eastern part of the province of Guangdong in southern China. Total concentrations of ∑PAHs were 29.38-815.46ng/g (dry weight), with a mean of 421.48ng/g. The composition of PAHs was characterized by an abundance of low molecular weight PAHs (2-3 benzenoid ring), and Phenanthrene (PHE), Anthracene (AN) and Fluoranthene (FA) were the predominant constituents. PAHs in this area appear to have mainly originated from petroleum sources and the combustion of grass, wood, and coal. PAHs in surface sediments of Zhelin Bay had a 9% incidence of causing adverse biological effects on aquatic organisms, according to the mean effects range-median quotient. PMID:27287864

  7. Monitoring Recovery of Prince William Sound, Alaska, Following the Exxon Valdez Oil Spill: Bioavailability of PAH in Offshore Sediments

    SciTech Connect

    Neff, Jerry M.; Boehm, Paul D.; Kropp, Roy K.; Stubblefield, William A.; Page, David S.

    2004-11-02

    We determined the bioavailability to sediment dwelling marine worms of polycyclic aromatic hydrocarbons (PAHs) associated with offshore sediments from 3 spill path and 3 non-spill path areas of Prince William Sound (PWS), Alaska, 12 years after the Exxon Valdez oil spill. The PAHs in sediments from 4 sites sampled in 2001 were primarily from a regional natural petrogenic background derived from organic-rich shales and natural oil seeps associated with sources southeast of PWS. Pyrogenic (combustion) PAHs, primarily from former human and industrial activities, were more abundant than petrogenic PAHs in nearshore sediments from 2 bays associated with past and current human activities. We performed sediment bioaccumulation tests with the six sediments and polychaete worms according to standard EPA protocols. All the PAHs had a very low bioavailability, as indicated by low values for biota/sediment accumulation factors (BSAFs) in the worms. Mean BSAFs for total PAHs (sum of 41 analyte groups) ranged from 0.002 to 0.009. The worms exposed to spill path and non-spill path sediments bioaccumulated small amounts of 4- and 5-ring PAHs, particularly fluoranthene and pyrene; these higher molecular weight PAHs are responsible for induction of mixed function oxygenase (MFO) activity in marine fish, birds, and mammals. These results may help to explain in part why fish from throughout PWS exhibit induced MFO activity. Elevated levels of MFO activity cannot be used as evidence of recent exposure by marine fish, birds, and mammals in the sound to Exxon Valdez oil.

  8. PAH contamination in soils adjacent to a coal-transporting facility in Tapin district, south Kalimantan, Indonesia.

    PubMed

    Mizwar, Andy; Trihadiningrum, Yulinah

    2015-07-01

    This study was undertaken to determine the level of 16 polycyclic aromatic hydrocarbon (PAH), listed as priority pollutants by the United States Environmental Protection Agency (USEPA), in surface soils around a coal-transporting facility in the western part of South Kalimantan, Indonesia. Three composite soil samples were collected from a coal stockpile, coal-hauling road, and coal port. Identification and quantification of PAH was performed by gas chromatography-mass spectrometry. The total content of 16 USEPA-PAH ranged from 11.79 to 55.30 mg/kg with arithmetic mean value of 33.14 mg/kg and median of 32.33 mg/kg. The 16 USEPA-PAH measured levels were found to be greater compared with most of the literature values. The levels of high molecular-weight PAH (5- and 6-ring) were dominant and formed 67.77-80.69 % of the total 16 USEPA-PAH The most abundant of individual PAH are indeno[1,2,3-cd] pyrene and benzo[a]pyrene with concentration ranges of 2.11-20.56 and 1.59-17.84 mg/kg, respectively. The degree of PAH contamination and subsequent toxicity assessment suggest that the soils of the study area are highly contaminated and pose a potential health risk to humans. PMID:25672272

  9. [Seasonal variation and function-area difference of PAHs in road dust from Shanghai urban area].

    PubMed

    Cheng, Shu-bo; Liu, Min; Ou, Dong-ni; Gao, Lei; Wang, Li-li; Xu, Shi-yuan

    2007-12-01

    Seasonal variation and function-area difference of polycyclic aromatic hydrocarbons (PAHs) in road dust from Shanghai centre area were studied, and the probable reasons were also discussed. The result showed that the accumulation level of PAHs varied significantly from winter to summer, namely, and the concentrations of total PAHs and the homologues in winter were higher than that in summer. Total PAH concentrations (t-PAH) in winter samples ranged from 9176 to 32,573 ng x g(-1), with a mean value of 20,648 ng x g(-1), whereas they varied from 6875 to 27,766 ng x g(-1) in summer, with an average of 14098 ng x g(-1). The individual PAHs composition ranged from 50 (acenaphthylene) to 3162 (indeno (1,2,3,-cd) pyrene) ng x g(-1) in winter, and 3 (acenaphthene) to 1485 (indeno(1,2,3,-cd) pyrene) ng x g(-1) in summer. The results exhibited that the levels showed a great rise from summer to winter. The difference of PAHs concentrations in road dust from functional areas were also obvious, that is, in winter, PAHs concentrations in road dust at industrial area (ID), commercial area (CO) and traffic area (TR) were much higher than those in other areas, with t-PAH mean concentration of 31 163, 24 932 and 18 815 ng x g(-1) resepectively, while city park (CP) and public lawn (PL) had the lowest level (7885, 8036 ng x g(-1)). In summer, the lowest concentration (7942 ng x g(-1)) appeared in CP, however, TR, ID and CO were the most polluted areas, with t-PAH mean concentration of 14,528, 14,247 and 11,523 ng x g(-1), respectively. The concentration of PAH homologues raised gradually with the ring number or molecular weight. Seasonal variation and function-area difference of PAHs in road dust from urban area correlated with both their sources and their physical and chemical characteristics. PMID:18290438

  10. Impact of electrochemical treatment of soil washing solution on PAH degradation efficiency and soil respirometry.

    PubMed

    Mousset, Emmanuel; Huguenot, David; van Hullebusch, Eric D; Oturan, Nihal; Guibaud, Gilles; Esposito, Giovanni; Oturan, Mehmet A

    2016-04-01

    The remediation of a genuinely PAH-contaminated soil was performed, for the first time, through a new and complete investigation, including PAH extraction followed by advanced oxidation treatment of the washing solution and its recirculation, and an analysis of the impact of the PAH extraction on soil respirometry. The study has been performed on the remediation of genuine PAH-contaminated soil, in the following three steps: (i) PAH extraction with soil washing (SW) techniques, (ii) PAH degradation with an electro-Fenton (EF) process, and (iii) recirculation of the partially oxidized effluent for another SW cycle. The following criteria were monitored during the successive washing cycles: PAH extraction efficiency, PAH oxidation rates and yields, extracting agent recovery, soil microbial activity, and pH of soil. Two representative extracting agents were compared: hydroxypropyl-beta-cyclodextrin (HPCD) and a non-ionic surfactant, Tween(®) 80. Six PAH with different numbers of rings were monitored: acenaphthene (ACE), phenanthrene (PHE), fluoranthene (FLA), pyrene (PYR), benzo(a)pyrene (BaP), and benzo(g,h,i)perylene (BghiP). Tween(®) 80 showed much better PAH extraction efficiency (after several SW cycles) than HPCD, regardless of the number of washing cycles. Based on successive SW experiments, a new mathematical relation taking into account the soil/water partition coefficient (Kd*) was established, and could predict the amount of each PAH extracted by the surfactant with a good correlation with experimental results (R(2) > 0.975). More HPCD was recovered (89%) than Tween(®) 80 (79%), while the monitored pollutants were completely degraded (>99%) after 4 h and 8 h, respectively. Even after being washed with partially oxidized solutions, the Tween(®) 80 solutions extracted significantly more PAH than HPCD and promoted better soil microbial activity, with higher oxygen consumption rates. Moreover, neither the oxidation by-products nor the acidic media (p

  11. Persistence of polycyclic aromatic hydrocarbons (PAHs) in biochar-amended soil.

    PubMed

    Kuśmierz, Marcin; Oleszczuk, Patryk; Kraska, Piotr; Pałys, Edward; Andruszczak, Sylwia

    2016-03-01

    In the present study the persistence of polycyclic aromatic hydrocarbons (PAHs) applied with biochar to acidic soil (loamy sand) was studied in two and half year field experiment. An experiment was carried out in three experimental plots (15 m(2) each). The biochar was introduced in the following doses: soil without fertilization - control (C-BC00), soil with 30 t ha(-1) (B-BC30) and soil with 45 t ha(-1) (A-BC45) of biochar. Biochar addition to soils resulted in an increase in the PAHs content from 0.239 μg g(-1) in control soil to 0.526 μg g(-1) and 1.310 μg g(-1) in 30 and 45 t ha(-1) biochar-amended soil respectively. However during the experimental period the PAHs content decreased to a level characteristic for the control soil. The highest losses of PAHs were observed during the first 105 days of the experiment. Three and four rings PAHs were the most susceptible for degradation and leaching. Migration of PAHs from 0-10 cm to 10-20 cm soil horizon was also observed. PMID:26735727

  12. 2,2-Dimethyl-5-[(2-nitro-anilino)methyl-idene]-1,3-dioxane-4,6-dione.

    PubMed

    He, Yu-Xin; Wu, Jin-Wei; Tong, Rong-Sheng; Shi, Jian-You

    2011-05-01

    The crystal of the title compound, C(13)H(12)N(2)O(6), contains a bifurcated intra-molecular hydrogen bond between the N-H group and one of the O atoms from both the nitro group and the dioxane-4,6-dione moiety. In addition, mol-ecules are linked by a series of inter-molecular C-H⋯O secondary inter-actions. The dihedral angles between the benzene ring and the nitro group and the conjugated part of the dioxane-4,6-dione moiety are 19.1 (2) and 17.89 (7)°, respectively. PMID:21754514

  13. Saturn's rings

    NASA Technical Reports Server (NTRS)

    2000-01-01

    When seen from the unlit side, the rings of Saturn present a much different appearance from that familiar to telescopic observers. Relatively opaque areas like the B Ring turn black, while lightly populated zones, such as the C Ring and the Cassini Division, prove to excellent diffuse transmitters of sunlight. The A Ring, with intermediate opacity, is at an intermediate level of brightness.

  14. Synthesis and biological activity of nitro-substituted cyclopenta-fused PAH

    SciTech Connect

    Goldring, J.M.; Ball, L.M.; Sangaiah, R.; Gold, A.

    1986-08-01

    PAH containing a peripherally fused cyclopenta ring are genotoxically active in Salmonella and mammalian cells and have been identified in combustion emissions. Since the cyclopenta ring is predicted to be susceptible to electrophilic attack, nitrosubstituted cyclopenta-fused PAH may be formed in the presence of NO(x), particularly in diesel exhaust, and hence be present in the environment. Nitro derivatives of cyclopenta (cd) pyrene and the cyclopenta-fused benzanthracene isomers were prepared by reaction of the PAH with dinitrogen tetroxide. The purifed products were characterized by mass spectroscopy, (1)H NMR, UV-vis and HPLC. In all cases, nitro substitution occurred on the cyclopenta ring in accord with expectation. Preliminary assay in S. typhimurium indicates that 4-nitro-cyclopenta(cd)pyrene is mutagenically active without exogenous metabolic activation in nitroreductase-competent strains. The results of the study have allowed us to test the hypothesis and will aid in development of structure-activity relationships of nitroPAH.

  15. Catalytic Oxidation of Pahs in Wastewater / Katalityczne Utlenianie Wwa w Ściekach

    NASA Astrophysics Data System (ADS)

    Turek, Agnieszka; Włodarczyk-Makuła, Maria

    2016-03-01

    The aim of the investigations was to determine the effectiveness of the removal of 4, 5 - ring PAHs from coking wastewater using dihydrogen dioxide in the presence of a cobalt, platinum or titanium catalyst. A dose 7.4 mL of dihydrogen dioxide in the amount of and 14.8 mL/L of the analyzed sample were added to the samples. The samples were shaken and stored under laboratory conditions for 12 hours. The concentration of PAHs before and after the oxidation process were determined. The quantitative and qualitative chromatographic analysis was carried out using a gas chromatograph coupled with a mass spectrometer (GC-MS). The total concentration of 8 PAHs before oxidation reached the value of 9150 ng/L The concentration of 4-ring compounds and 5-ring PAHs were equal to 6390 ng/L and 2760 ng/L, respectively. The highest decrease (93%) the sum of 8 hydrocarbons using a dose of oxidizer 7.4 ml/L and in the presence of titanium catalyst was achieved.

  16. Coupling extraction-flotation with surfactant and electrochemical degradation for the treatment of PAH contaminated hazardous wastes.

    PubMed

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

    2009-10-30

    The performance of a two-stage process combining extraction of polycyclic aromatic hydrocarbons (PAHs) with an amphoteric surfactant (CAS) followed by electro-oxidation of PAH-foam concentrate was studied for the decontamination of aluminum industry wastes (AIW) and polluted soils. The PAH suspensions extracted from AIW and soils were treated in a 2L-parallelepipedic electrolytic cell containing Ti/RuO2 anodes and stainless steel cathodes. Current densities varying from 4.6 to 18.5 mA cm(-2) have been tested with and without addition of a supporting electrolyte (6.25 to 50 kg Na2SO4 t(-1) of dry waste). The best performance for PAH degradation was obtained while the electrolytic cell was operated during 90 min at a current density of 9.2 mA cm(-2), with a total solids concentration of 2.0%, and in presence 12.5 kg Na(2)SO(4)t(-1). The application of the process on AIW (initial PAH content: 3424 mg kg(-1)) allowed extracting 42% of PAH, whereas 50% of PAH was electrochemically degraded in the resulting foam suspensions. By comparison, 44% to 60% of PAH was extracted from polluted soils (initial PAH content: 1758 to 4160 mg kg(-1)) and 21% to 55% of PAH was oxidized in the foam suspensions. The electrochemical treatment cost (including only electrolyte and energy consumption) recorded in the best experimental conditions varied from 99 to 188 USD $ t(-1) of soils or AIW treated. PMID:19525064

  17. Kinetic studies of the hydroxyl radical reaction with PAHs

    NASA Astrophysics Data System (ADS)

    Ananthula, Rajeshwar

    An existing quartz optical reactor heating system was designed to permit higher temperature kinetic measurements more closely associated with post-combuston conditions (up to 1200 K). A pulsed laser photolysis/pulsed laser-induced fluorescence (PLP/PLIF) technique was then applied with this modified reactor to study the OH radical kinetics with polycyclic aromatic hydrocarbons (PAHs). The kinetics of the reaction of a surrogate three-ring PAH, anthracene (and its deuterated form) with hydroxyl (OH) radicals was investigated over the temperature range of 373 to 1200 K. This study represents the first examination of the OH kinetics for this class of reactions at elevated temperatures (>470 K). The results indicate a complex temperature dependence similar to that observed for simpler aromatic compounds, e.g., benzene. At low temperatures (373-498 K), the rate measurements exhibited Arrhenius behavior (1.82 x 10-11 exp(542.35/T) in units of cm3 molecule -1 s-1) and kinetic isotope effect (KIE) measurements were consistent with an OH addition mechanism. The low temperature results are extrapolated to atmospheric temperatures and compared with previous measurements. Rate measurements between 673 and 923 K exhibited a sharp decrease in the magnitude of the rate coefficients (a factor of 9). KIE measurements under these conditions were still consistent with an OH addition mechanism. The following modified Arrhenius equation is the best fit to our anthracene measurements between 373 and 923 K, 8.17 x 1014 T-8.3 exp(-3171.71/T) (in units of cm3 molecule-1 s-1). For a limited temperature range between 1000 and 1200 K, the rate measurements exhibited an apparent positive temperature dependence with the following Arrhenius equation the best fit to the data, 2.18 x 10-11*exp(-1734.11/T) (in units of cm3molecule-1s -1). KIE measurements above 999 K were slightly larger than unity, but inclusive regarding the mechanism of the reaction. Theoretical calculations of the KIE indicate

  18. Reduction of Toxicity and PAH Bioaccumulation Potential During Bioremediation of Petroleum Contaminated Soils

    SciTech Connect

    Huesemann, Michael H.; Hausmann, Tom S.; Fortman, Timothy J.

    2004-03-01

    A set of model soils (e.g., quartz sands, loams, clays, peat, silica gels) was spiked with crude oil, aged for 27 months in the laboratory, and subjected to bench-scale slurry bioremediation treatment for 90 weeks. At various times, slurry samples were removed from the bioreactors, analyzed for polynuclear aromatic hydrocarbons (PAHs), and assayed for toxicity using the solid-phase MicrotoxTM test. In addition, the PAH bioaccumulation potential in tissues of soil dwelling organisms was estimated by exposing semi-permeable membrane devices (SPMDs) for 14 days to initial (t=0) and final (t=90 wks) slurry samples. In most cases, soil toxicity (EC50) was reduced 5- to 10 fold during the first 20 weeks of bioremediation treatment but it rarely reached the EC50 value of the respective clean reference soils, indicating that some residual toxicity still remained after 20 weeks of bioremediation. The reduction of soil toxicity most closely correlated with the biodegradation of the sum of 4, 5, and 6 ring PAHs. A comparison of PAH concentrations in SPMDs exposed to initial and final slurry samples revealed that the potential of PAH accumulation in exposed animal tissues was reduced 50 to 300 fold as a result of slurry biotreatment. While in most soils the bioavailable PAH fraction was preferentially removed by the microorganisms, several high molecular weight PAHs that had reached an apparent concentration asymptote after 90 weeks of treatment were still bioavailable to a significant extent in several soils since they were readily taken up by the SPMDs. In summary, it can be concluded that bioremediation significantly reduces both toxicity and PAH bioaccumulation potential. However, the remaining undegraded contaminants are likely to pose some residual risk to environmental receptors since they still exhibit toxicity relative to uncontaminated background soils and are bioavailable to animal tissues.

  19. Aerobic Bioremediation of PAH Contaminated Soil Results in Increased Genotoxicity and Developmental Toxicity.

    PubMed

    Chibwe, Leah; Geier, Mitra C; Nakamura, Jun; Tanguay, Robert L; Aitken, Michael D; Simonich, Staci L Massey

    2015-12-01

    The formation of more polar and toxic polycyclic aromatic hydrocarbon (PAH) transformation products is one of the concerns associated with the bioremediation of PAH-contaminated soils. Soil contaminated with coal tar (prebioremediation) from a former manufactured gas plant (MGP) site was treated in a laboratory scale bioreactor (postbioremediation) and extracted using pressurized liquid extraction. The soil extracts were fractionated, based on polarity, and analyzed for 88 PAHs (unsubstituted, oxygenated, nitrated, and heterocyclic PAHs). The PAH concentrations in the soil tested, postbioremediation, were lower than their regulatory maximum allowable concentrations (MACs), with the exception of the higher molecular weight PAHs (BaA, BkF, BbF, BaP, and IcdP), most of which did not undergo significant biodegradation. The soil extract fractions were tested for genotoxicity using the DT40 chicken lymphocyte bioassay and developmental toxicity using the embryonic zebrafish (Danio rerio) bioassay. A statistically significant increase in genotoxicity was measured in the unfractionated soil extract, as well as in four polar soil extract fractions, postbioremediation (p < 0.05). In addition, a statistically significant increase in developmental toxicity was measured in one polar soil extract fraction, postbioremediation (p < 0.05). A series of morphological abnormalities, including peculiar caudal fin malformations and hyperpigmentation in the tail, were measured in several soil extract fractions in embryonic zebrafish, both pre- and postbioremediation. The increased toxicity measured postbioremediation is not likely due to the 88 PAHs measured in this study (including quinones), because most were not present in the toxic polar fractions and/or because their concentrations did not increase postbioremediation. However, the increased toxicity measured postbioremediation is likely due to hydroxylated and carboxylated transformation products of the 3- and 4-ring PAHs (PHE, 1

  20. Polycyclic aromatic hydrocarbons (PAHs) in aerosols over the central Himalayas along two south-north transects

    NASA Astrophysics Data System (ADS)

    Chen, Pengfei; Li, Chaoliu; Kang, Shichang; Rupakheti, Maheswar; Panday, Arnico K.; Zhang, Qianggong

    2016-04-01

    Our understanding of the transport of polycyclic aromatic hydrocarbons (PAHs) from the Indo-Gangetic Plains (IGP) to the Himalayas remains limited. Concentrations of PAHs were therefore measured in total suspended particles (TSP) from six sites along two south-north transects across the central Himalayas. Spatially, the annual average TSP and PAH (especially 5- and 6-ring) concentrations were found to decrease noticeably along both transects. The dry deposition fluxes had similar distribution pattern with the ambient PAH levels. Moreover, annual TSP and PAH concentrations exhibited a logarithmic decreasing pattern with increasing elevation especially in the non-monsoon seasons (TSP: y=-57.3lnx+552, R2=0.952; PAHs: y=-26.8lnx+229, R2=0.948). The TSP and PAH concentrations showed a clear seasonal variation, with the minimum concentrations around the mid-monsoon season and the maximum concentrations in winter season at Lumbini and Pokhara. While at other remote sites these pollutants were slightly higher during the non-monsoon season than those in the monsoon season. The diagnostic ratio suggested that atmospheric PAHs from the Nepal sites were mainly associated with emission of biomass, coal burning and petroleum combustion. A similar composition pattern was found between the two sides of the Himalayas, suggesting that the northern side of the Himalayas may be affected by anthropogenic emissions from the IGP due to long-range transportation as well as the unique mountain/valley breeze system which bring pollution from the IGP into Tibet across the high Himalayas.

  1. PAHs and the Diffuse Interstellar Bands. What have we Learned from the New Generation of Laboratory and Observational Studies?

    NASA Technical Reports Server (NTRS)

    Salama, Farid

    2005-01-01

    precursors in an isolated environment at low temperature (of the order of 100 K). The spectra of neutral and ionized PAHs are measured using the high sensitivity methods of cavity ring down spectroscopy (CRDS). These experiments provide unique information on the spectra of free, cold large carbon molecules and ions in the gas phase. Intrinsic band profiles and band positions of cold gas-phase PAHs can now be measured with high- sensitivity spectroscopy and directly compared to the astronomical data. The electronic bands measured for ionized PAH are found to be intrinsically broad (about 20/cm) while the bands associated with the neutral precursors are narrower (of the order of 2 - 10/cm).

  2. UV action spectroscopy of protonated PAH derivatives. Methyl substituted quinolines

    NASA Astrophysics Data System (ADS)

    Klærke, B.; Holm, A. I. S.; Andersen, L. H.

    2011-08-01

    Aims: We investigate the production of molecular photofragments upon UV excitation of PAH derivatives, relevant for the interstellar medium. Methods: The action absorption spectra of protonated gas-phase methyl-substituted quinolines (CH3 - C9H7NH+) have been recorded in the 215-338 nm spectral range using the electrostatic storage ring ELISA, an electrospray ion source and 3 ns UV laser pulses. Results: It is shown that the absorption profile is both redshifted and broadened when moving the methyl group from the heterocycle containing nitrogen to the homoatomic ring. The absorption profiles are explained by TD-DFT calculations. The dissociation time of the studied molecules is found to be of several milliseconds at 230 nm and it is shown that after redistribution of the absorbed energy the molecules dissociate in several channels. The dissociation time found is an order of magnitude faster than the estimated IR relaxation time. Photophysical properties of both nitrogen containing and methyl-substituted PAHs are interesting in an astrophysical context in connection with identifying the aromatic component of the interstellar medium.

  3. Creating Sacred Places for Children in Grades 4-6.

    ERIC Educational Resources Information Center

    Fox, Sandra J.

    This guide attempts to help teachers of American Indian children in grades 4-6 provide a culturally relevant education that takes place in the regular classroom, includes content related to Indian students' lives, makes students proud, expands to other experiences, and enhances learning. Creating sacred places means responding appropriately to…

  4. Teachers Guide to Economic Concepts: Grade 4-6.

    ERIC Educational Resources Information Center

    McCabe, Milo F.

    This grades 4-6 teachers guide is one of five resource guides developed to aid teachers in helping students in South Dakota to achieve a high degree of economic literacy. It is felt that schools must prepare students at all grade levels to develop an understanding of the economy in which they live. This guide was specifically prepared to assist…

  5. Health Promotion Activity Book for Grades 4-6.

    ERIC Educational Resources Information Center

    Ohio State Dept. of Health, Columbus.

    This book of activities is designed to supplement health lessons for students in grades 4-6. Some of the activities are quite simple and require very little instruction and direction, while others are more difficult and require careful explanation prior to completion. The level of difficulty of the activities is varied in order to create both…

  6. 2,4,6-TRINITROTOLUENE TRANSFORMATION IN PLANTED, SOIL COLUMNS

    EPA Science Inventory

    2,4,6-Trinitrotoluene (TNT), has been used extensively by the United States military to manufacture explosive devices. Since the conclusion of World War 11, many of these military installations have also been involved in the disposal of surplus and outdated explosives. Both the c...

  7. 4,6-Dinitro-o-cyclohexyl phenol

    Integrated Risk Information System (IRIS)

    4,6 - Dinitro - o - cyclohexyl phenol ; CASRN 131 - 89 - 5 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments

  8. Learn about Seabirds. Teaching Packet, Grades 4-6.

    ERIC Educational Resources Information Center

    Fish and Wildlife Service (Dept. of Interior), Anchorage, AK.

    This teaching packet is designed to teach Alaskan students in grades 4-6 about Alaska's seabird populations, the worldwide significance of seabirds, and the environmental conditions to which seabirds are sensitive. The packet includes a curriculum guide (containing a teacher's background story and 12 teaching activities), a separately published…

  9. Traffic Safety Education for Oregon Schools, 4-6.

    ERIC Educational Resources Information Center

    Oregon State Dept. of Education, Salem.

    Instructional materials for teaching traffic safety education to Grades 4-6 students are presented in the document. The learning activities, which are presented separately for each level, focus on the goals of functioning as responsible citizens as pedestrians, bicyclists, car passengers, and school bus passengers. A series of 15 lessons are…

  10. 11. DETAILS: CONCRETE SHEET PILING, CORNERS #4 & #6, DWG. ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    11. DETAILS: CONCRETE SHEET PILING, CORNERS #4 & #6, DWG. NO. 11, 1-1/2" = 1 FT., FEB. 12, 1908, MADE BY E.C.L., APPROVED BY O.F. LACKEY - Baltimore Inner Harbor, Pier 5, South of Pratt Street between Market Place & Concord Street, Baltimore, Independent City, MD

  11. 4.6 Doses to Patients in Therapy

    NASA Astrophysics Data System (ADS)

    Noßke, D.; Mattsson, S.; Johansson, L.

    This document is part of Subvolume A 'Fundamentals and Data in Radiobiology, Radiation Biophysics, Dosimetry and Medical Radiological Protection' of Volume 7 'Medical Radiological Physics' of Landolt-Börnstein - Group VIII 'Advanced Materials and Technologies'. It contains the Section '4.6 Doses to Patients in Therapy' of the Chapter '4 Dosimetry in Nuclear Medicine Diagnosis and Therapy' with the contents:

  12. Council Minutes, February 4-6, 2011: Santa Monica, California

    ERIC Educational Resources Information Center

    Educational Researcher, 2011

    2011-01-01

    This article presents minutes of the American Educational Research Association's meetings held in Santa Monica, California, on February 4-6, 2011. President Kris D. Gutierrez led a discussion of the meeting dates for the summer Executive Board and Council meetings. It was agreed that members of Council will be polled to determine the best dates…

  13. 2,2-Dimethyl-5-(2-nitro-benzyl-idene)-1,3-dioxane-4,6-dione.

    PubMed

    García-Álvarez, Fernando; Romero, Nancy; Lobato-García, Carlos E; Terán, Joel L; Mendoza, Angel

    2013-01-01

    The asymmetric unit of the title compound, C13H11NO6, contains two mol-ecules in both of which the six-membered 1,3-dioxane-4,6-dione ring shows a screw-boat conformation. The dihedral angles between the best planes through the six-membered rings are 47.8 (2) and 49.8 (2)°. In the crystal, C-H⋯O inter-actions link the mol-ecules, building a supramolecular sheet parallel to the c axis. PMID:23476434

  14. Relationships between indoor and outdoor air pollution by carcinogenic PAHs and PCBs

    NASA Astrophysics Data System (ADS)

    Menichini, E.; Iacovella, N.; Monfredini, F.; Turrio-Baldassarri, L.

    PAHs and PCBs were collected simultaneously indoors and outdoors at eight non-smoking homes located in four buildings in high-traffic areas of Rome. The purpose was to evaluate the relevance of indoor air in contributing to the overall exposure of the urban population. The vertical distribution was also investigated by collecting outdoor samples at both road and roof level, and indoor samples in both a high and a low floor flat of each building. At one coal-heated building, samples were collected during both the heating and the non-heating season. No evident PAH source was present indoors. Indoor and outdoor daily concentrations of benzo[a]pyrene (BaP) ranged, respectively, 0.1-4.6 ng m -3 and 0.7-2.3 ng m -3. With the heating on, indoor PAH concentrations equalled or exceeded those outdoors, with BaP indoor/outdoor ratios up to 4; during the warm season, ratios decreased to 0.2-0.6. Indoor PAHs at the low floors exceeded the high-floor ones when the heating was off (vehicle exhausts being the dominant source), while being equal or lower with the heating on; the vertical gradient of indoor PAHs between different floors was within a factor of 2. Outdoor PAHs at roof level were 20-70% of those at road level, which in turn exceeded those at the medium-traffic station up to a factor of 4. The outdoor concentrations of Σ6 indicator PCBs ranged 0.1-1.6 ng m -3. Indoor PCB concentrations exceeded those outdoors by an approximate factor of 2-50. No vertical gradient was observed. The results indicated that indoor air may contribute to the overall exposure to PAHs and PCBs more than the urban air. They were also consistent with recent findings suggesting that indoor air can be a relevant source of PCBs for outdoor air.

  15. Saturn's Rings

    NASA Astrophysics Data System (ADS)

    Cuzzi, J. N.

    2014-12-01

    The rings are changing before our eyes; structure varies on all timescales and unexpected things have been discovered. Many questions have been answered, but some answers remain elusive (see Cuzzi et al 2010 for a review). Here we highlight the major ring science progress over the mission to date, and describe new observations planned for Cassini's final three years. Ring Composition and particle sizes: The rings are nearly all water ice with no other ices - so why are they reddish? The C Ring and Cassini Division are "dirtier" than the more massive B and A Rings, as shown by near-IR and, recently, microwave observations. Particle sizes, from stellar and radio occultations, vary from place to place. Ring structure, micro and macro: numerous spiral density waves and ubiquitous "self-gravity wakes" reveal processes which fostered planet formation in the solar system and elsewhere. However, big puzzles remain regarding the main ring divisions, the C Ring plateau structures, and the B Ring irregular structure. Moonlets, inside and out, seen and unseen: Two gaps contain sizeable moonlets, but more gaps seem to contain none; even smaller embedded "propeller" objects wander, systematically or randomly, through the A ring. Rubble pile ringmoons just outside the rings may escaped from the rings, and the recently discovered "Peggy" may be trying this as we watch. Impact bombardment of the rings: Comet fragments set the rings to rippling on century-timescales, and boulders crash through hourly; meanwhile, the constant hail of infalling Kuiper belt material has a lower mass flux than previously thought. Origin and Age of the Rings: The ring mass and bombardment play key roles. The ring mass is well known everywhere but in the B Ring (where most of it is). New models suggest how tidal breakup of evolving moons may have formed massive ancient rings, of which the current ring is just a shadow. During its last three years, the Cassini tour profile will allow entirely new

  16. Levels and sources of PAHs in selected sites from Portugal: biomonitoring with Pinus pinea and Pinus pinaster needles.

    PubMed

    Ratola, Nuno; Amigo, José Manuel; Alves, Arminda

    2010-04-01

    Pine needle samples from two pine species (Pinus pinaster Ait. and Pinus pinea L.) were collected at 29 sites scattered throughout Portugal, in order to biomonitor the levels and trends of 16 polycyclic aromatic hydrocarbons (PAHs). The values obtained for the sum of all PAHs ranged from 76 to 1944 ng/g [dry weight (dw)]. Despite the apparent matrix similarities between both pine species, P. pinaster needles revealed higher mean entrapment levels than P. pinea (748 and 399 ng/g (dw) per site, respectively). The urban and industrial sites have the highest average of PAH incidence [for P. pinea, 465 and 433 ng/g (dw) per site, respectively, and for P. pinaster, 1147 and 915 ng/g (dw)], followed by the rural sites [233 ng/g and 711 ng/g (dw) per site, for P. pinea and P. pinaster, respectively]. The remote sites, both from P. pinaster needles, show the least contamination, with 77 ng/g (dw) per site. A predominance of 3-ring and 4-ring PAHs was observed in most samples, with phenanthrene having 30.1% of the total. Naphthalene prevailed in remote sites. Rainfall had no influence on the PAHs levels, but there was a relationship between higher wind speeds and lower concentrations. PAH molecular ratios revealed the influence of both petrogenic and pyrogenic sources. PMID:20107982

  17. 5-(3,4-Dimethyl-benzyl-idene)-2,2-dimethyl-1,3-dioxane-4,6-dione.

    PubMed

    Zeng, Wu-Lan

    2011-06-01

    The title compound, C(15)H(16)O(4), was prepared by the reaction of 2,2-dimethyl-1,3-dioxane-4,6-dione and 3,4-dimethyl-benzaldehyde in ethanol. The 1,3-dioxane ring exhibits an envelope conformation. In the crystal, mol-ecules are linked by weak inter-molecular C-H⋯O hydrogen bonds, forming chains parallel to the b axis. PMID:21754745

  18. Laser photo-oxidative degradation of 4,6-dimethyldibenzothiophene.

    PubMed

    Gondal, M A; Masoudi, H M; Pola, J

    2008-04-01

    Degradation of 4,6-dimethyldibenzothiophene (DMDBT), persistent sulfur contaminant in fuel oils has been achieved in non-polar phase by laser-irradiating DMDBT alone and in the presence of hydrogen peroxide and molecular oxygen. The most efficient degradation in the presence of molecular oxygen is judged to be the first example of self-sensitized photo-oxygenation of thiophenes, in which DMDBT sequentially acts as 1O2 sensitizer and reactant. PMID:18308366

  19. Infrared fluorescence from PAHs in the laboratory

    NASA Technical Reports Server (NTRS)

    Cherchneff, Isabelle; Barker, John R.

    1989-01-01

    Several celestial objects, including UV rich regions of planetary and reflection nebulae, stars, H II regions, and extragalactic sources, are characterized by the unidentified infrared emission bands (UIR bands). A few years ago, it was proposed that polycyclic aromatic hydrocarbon species (PAHs) are responsible for most of the UIR bands. This hypothesis is based on a spectrum analysis of the observed features. Comparisons of observed IR spectra with lab absorption spectra of PAHs support the PAH hypothesis. An example spectrum is represented, where the Orion Bar 3.3 micron spectrum is compared with the absorption frequencies of the PAHs Chrysene, Pyrene, and Coronene. The laser excited 3.3 micron emission spectrum is presented from a gas phase PAH (azulen). The infrared fluorescence theory (IRF) is briefly explained, followed by a description of the experimental apparatus, a report of the results, and discussion.

  20. Vascular ring

    MedlinePlus

    ... with aberrant subclavian and left ligamentum ateriosus; Congenital heart defect - vascular ring; Birth defect heart - vascular ring ... accounts for less than 1% of all congenital heart problems. The condition occurs as often in males ...

  1. Neptune's rings

    NASA Technical Reports Server (NTRS)

    1999-01-01

    This 591-second exposure of the rings of Neptune were taken with the clear filter by the Voyager 2 wide-angle camera. The two main rings are clearly visible and appear complete over the region imaged. Also visible in this image is the inner faint ring and the faint band which extends smoothly from the ring roughly halfway between the two bright rings. Both of these newly discovered rings are broad and much fainter than the two narrow rings. The bright glare is due to over-exposure of the crescent on Neptune. Numerous bright stars are evident in the background. Both bright rings have material throughout their entire orbit, and are therefore continuous. The Voyager Mission is conducted by JPL for NASA's Office of Space Science and Applications.

  2. Developing PAHs as Probes of Physical Conditions: Fitting PAH Spectra with the Ames PAH IR Spectral Database

    NASA Astrophysics Data System (ADS)

    Allamandola, Louis

    It is quite clear from the Infrared Space Observatory (ISO) and Spitzer Space Telescope results that we live in a molecular universe and that the mid-infrared is aglow in emission from polycyclic aromatic hydrocarbons (PAHs). Observationally, PAHs are easily identified by their characteristic emission spectrum, they are intrinsically strong emitters, and they dominate the emission in star forming galaxies in the mid-infrared, comprising 10-20% of the energy emitted in the infrared. These characteristics make them useful probes even for distant objects. The exceptional spectra provided by the ISO and Spitzer observatories have revealed in detail how the PAH features vary between different classes of objects and spatially within extended objects, showing that the details in the emission spectrum depend on the specific PAH molecules present, their size, ionization state, structure etc., and therefore reflect conditions within the emission zones. Thus, understanding the origin and evolution of this important family of molecules, how they interact with and control their environment, and how the details in their emission spectra reflect local conditions, is a fundamental goal of astrophysics. Advances in laboratory studies and computer-based calculations of PAHs now allow us to delve into the details of PAH spectral behavior seen by both ISO and Spitzer. We propose to model PAH spectra observed in reflection nebulae, HII regions, planetary nebulae, YSOs, AGB stars, and galaxies using laboratory and theoretically generated spectra from the NASA Ames PAH IR Spectroscopic Database to advance our understanding of the factors that determine the PAH spectra that we see in objects both near and far.

  3. Source apportionment of PAHs in surface sediments using positive matrix factorization combined with GIS for the estuarine area of the Yangtze River, China.

    PubMed

    Yu, Wenwen; Liu, Ruimin; Wang, Jiawei; Xu, Fei; Shen, Zhenyao

    2015-09-01

    This study used PMF and geostatistics to quantify sources of PAHs based on 30 samples tested for 16 PAHs in surface sediment from the Yangtze River Estuary (YRE) in February 2011. The results demonstrated that the total PAH concentrations varied from 65.07 to 954.52 ng g(-1) with a mean value of 224.00 ng g(-1). In the inner estuary, the mean of the total PAH concentrations was 229.89 ng g(-1), and the high molecular weight of four-to-six-ring PAHs accounted for 51.83% of PAHs. In the adjacent East Sea, the mean value was 218.85 ng g(-1) and the high molecular weight PAHs accounted for approximately 54% of total PAHs. A three-factor modeling result from PMF provided the most satisfactory analysis of PAH sources. Coke plant emissions and biomass combustion, which contributed 45.64% of the pollution, were the most important sources, and pollutants from these sources were primarily concentrated in the southern branch of the estuary. Gasoline fuel combustion accounted for approximately 40% of the pollution, and the major contaminated area was in the northern region. Petrogenic sources (14.70%) also influenced the estuary, especially in the northeastern region. Water currents and source locations affected the impacted regions of PMF factors; the surrounding natural and artificial influences were also considered. PMID:25966456

  4. Potential of Endophytic Bacterium Paenibacillus sp. PHE-3 Isolated from Plantago asiatica L. for Reduction of PAH Contamination in Plant Tissues.

    PubMed

    Zhu, Xuezhu; Jin, Li; Sun, Kai; Li, Shuang; Ling, Wanting; Li, Xuelin

    2016-01-01

    Endophytes are ubiquitous in plants, and they may have a natural capacity to biodegrade polycyclic aromatic hydrocarbons (PAHs). In our study, a phenanthrene-degrading endophytic Paenibacillus sp. PHE-3 was isolated from P. asiatica L. grown in a PAH-contaminated site. The effects of environmental variables on phenanthrene biodegradation by strain PHE-3 were studied, and the ability of strain PHE-3 to use high molecular weight PAH (HMW-PAH) as a sole carbon source was also evaluated. Our results indicated that pH value of 4.0-8.0, temperature of 30 °C-42 °C, initial phenanthrene concentration less than 100 mg·L(-1), and some additional nutrients are favorable for the biodegradation of phenanthrene by strain PHE-3. The maximum biodegradation efficiency of phenanthrene was achieved at 99.9% after 84 h cultivation with additional glutamate. Moreover, the phenanthrene biodegradation by strain PHE-3 was positively correlated with the catechol 2,3-dioxygenase activity (ρ = 0.981, p < 0.05), suggesting that strain PHE-3 had the capability of degrading HMW-PAHs. In the presence of other 2-, 3-ringed PAHs, strain PHE-3 effectively degraded HMW-PAHs through co-metabolism. The results of this study are beneficial in that the re-colonization potential and PAH degradation performance of endophytic Paenibacillus sp. PHE-3 may be applied towards reducing PAH contamination in plants. PMID:27347988

  5. Potential of Endophytic Bacterium Paenibacillus sp. PHE-3 Isolated from Plantago asiatica L. for Reduction of PAH Contamination in Plant Tissues

    PubMed Central

    Zhu, Xuezhu; Jin, Li; Sun, Kai; Li, Shuang; Ling, Wanting; Li, Xuelin

    2016-01-01

    Endophytes are ubiquitous in plants, and they may have a natural capacity to biodegrade polycyclic aromatic hydrocarbons (PAHs). In our study, a phenanthrene-degrading endophytic Paenibacillus sp. PHE-3 was isolated from P. asiatica L. grown in a PAH-contaminated site. The effects of environmental variables on phenanthrene biodegradation by strain PHE-3 were studied, and the ability of strain PHE-3 to use high molecular weight PAH (HMW-PAH) as a sole carbon source was also evaluated. Our results indicated that pH value of 4.0–8.0, temperature of 30 °C–42 °C, initial phenanthrene concentration less than 100 mg·L−1, and some additional nutrients are favorable for the biodegradation of phenanthrene by strain PHE-3. The maximum biodegradation efficiency of phenanthrene was achieved at 99.9% after 84 h cultivation with additional glutamate. Moreover, the phenanthrene biodegradation by strain PHE-3 was positively correlated with the catechol 2,3-dioxygenase activity (ρ = 0.981, p < 0.05), suggesting that strain PHE-3 had the capability of degrading HMW-PAHs. In the presence of other 2-, 3-ringed PAHs, strain PHE-3 effectively degraded HMW-PAHs through co-metabolism. The results of this study are beneficial in that the re-colonization potential and PAH degradation performance of endophytic Paenibacillus sp. PHE-3 may be applied towards reducing PAH contamination in plants. PMID:27347988

  6. Hydrogen-bonded supramolecular motifs in 2-amino-4,6-dimethoxypyrimidinium 4-hydroxybenzoate monohydrate, 2-amino-4,6-dimethoxypyrimidinium 6-carboxypyridine-2-carboxylate monohydrate and 2-amino-4,6-dimethoxypyrimidinium hydrogen (2R,3R)-tartrate 2-amino-4,6-dimethoxypyrimidine.

    PubMed

    Thanigaimani, Kaliyaperumal; Muthiah, Packianathan Thomas; Lynch, Daniel E

    2007-05-01

    In the crystal structures of the title compounds, C(6)H(10)N(3)O(2)+.C(7)H(5)O(3)-.H2O, (I), C(6)H(10)N(3)O(2)+.C(7)H(4)NO(4)-.H2O, (II), and C(6)H(10)N(3)O(2)+.C(4)H(5)O(6)-.C(6)H(9)N(3)O(2), (III), the 2-amino-4,6-dimethoxypyrimidinium cation [abbreviated as (MeO)2-Hampy+] interacts with the carboxylate group of the corresponding anion through a pair of nearly parallel N-H...O hydrogen bonds to form R(2)(2)(8) ring motifs. In (I), the (MeO)2-Hampy+ cation is centrosymmetrically paired through a pair of N-H...N hydrogen bonds involving the 2-amino group and a ring N atom forming an R(2)(2)(8) motif. In (II), inversion-related R(2)(2)(8) motifs (amino-pyrimidine-carboxylate motifs) are further bridged by N-H...O hydrogen bonds on either side forming a DDAA array of quadruple hydrogen bonds. This array is extended further on either side by O(water)-H...O(methoxy) hydrogen bonds, resulting in an array of six hydrogen bonds (ADDAAD). The water molecule plays a pivotal role, and five hydrogen-bonded fused rings are formed around the water molecule. In (III), the carboxy group of the tartrate anion interacts with the ring N atom and 2-amino group of the neutral (MeO)2-ampy molecule through N-H...O and O-H...N hydrogen bonds. There is also an intramolecular O-H...O hydrogen bond in the tartrate anion. In all three crystal structures, C-H...O hydrogen bonds are observed. PMID:17478916

  7. Emissions of PAHs derived from sugarcane burning and processing in Chiapas and Morelos México.

    PubMed

    Mugica-Alvarez, Violeta; Santiago-de la Rosa, Naxieli; Figueroa-Lara, Jesús; Flores-Rodríguez, Julio; Torres-Rodríguez, Miguel; Magaña-Reyes, Miguel

    2015-09-15

    Sugarcane burning is an agricultural practice implemented to ease farm worker duties; nevertheless, as a consequence, tons of particles are emitted to the atmosphere. Additionally, during harvesting the sugar-mills operate the whole day emitting hundreds of tons of pollutants. Therefore, health risks to neighboring population should be a major governmental concern, leading first to identification and quantification of toxic compounds, such as polycyclic aromatic hydrocarbons (PAHs). In order to establish the magnitude of the problem, four sampling campaigns of PM10 and PM2.5 were carried out in this study, during harvesting and no-harvesting seasons in two municipalities of México, with different climatic and social conditions. Concentrations of PM10, PM2.5, and organic compounds were determined daily, followed by extraction, identification and quantification of the 17 EPA-established PAHs from all samples. The results showed that during harvest, the PM10 mass increased lightly in Chiapas, but approximately twice in Morelos, whereas total PAH concentrations increased twice and six times, respectively. The most abundant PAHs, namely: indene [1,2,3cd] pyrene, benzo[b]fluoranthene, benzo[a]pyrene and dibenzo [a,h] anthracene are composed of 5 or more aromatic rings. Of the total PAHs quantified, 44% to 52% corresponded to carcinogenic compounds, consequently, the overall carcinogenic potential increased twice or three times. Principal component analysis with varimax rotation was applied to source apportionment at each site, suggesting three different sources during harvesting: the combustion process in the sugar mill, sugarcane burning and vehicular emissions. The combustion markers for sugar mill are, BAA, BBF, BKF, BAP, IND and BGP, whereas for sugarcane burning were ANT, PHE, FLT and PYR. The results obtained indicate that processing and burning sugarcane are the main sources of the PAH levels measured, proving that the health risks are boosted during harvesting

  8. Charcoal emissions as a source of CO and carcinogenic PAH in mainstream narghile waterpipe smoke.

    PubMed

    Monzer, Bassel; Sepetdjian, Elizabeth; Saliba, Najat; Shihadeh, Alan

    2008-09-01

    Burning charcoal is normally placed atop the tobacco to smoke the narghile waterpipe. We investigated the importance of charcoal as a toxicant source in the mainstream smoke, with particular attention to two well-known charcoal emissions: carbon monoxide (CO) and polyaromatic hydrocarbons (PAH). CO and PAH yields were compared when a waterpipe was machine smoked using charcoal and using an electrical heating element. The electrical heating element was designed to produce spatial and temporal temperature distributions similar to those measured using charcoal. With a popular type of ma'assel tobacco mixture, and using a smoking regimen consisting of 105 puffs of 530ml volume spaced 17s apart, it was found that approximately 90% of the CO and 75-92% of the 4- and 5-membered ring PAH compounds originated in the charcoal. Greater than 95% of the benzo(a)pyrene in the smoke was attributable to the charcoal. It was also found that the relative proportions of individual PAH species, the "PAH fingerprint", of the mainstream smoke were highly correlated to those extracted from the unburned charcoal (R(2)>0.94). In contrast, there was no correlation between the PAH fingerprint of the electrically heated and charcoal-heated conditions (R(2)<0.02). In addition to inhaling toxicants transferred from the tobacco, such as nicotine, "tar", and nitrosamines, waterpipe smokers thus also inhale large quantities of combustion-generated toxicants. This explains why, despite the generally low temperatures attained in the narghile tobacco, large quantities of CO and PAH have been found in the smoke. PMID:18573302

  9. Facilitated Bioavailability of PAHs to Native Soil Bacteria Promoted by Nutrient Addition

    NASA Astrophysics Data System (ADS)

    Pignatello, J. J.; Li, J.

    2006-12-01

    Facilitated bioavailability refers to the ability of an organism to have access to pools of non-labile chemical. Mechanisms proposed for this ability include release of biosurfactants, direct mining of adsorbed chemical, alteration of interfacial chemistry, and passive effects of attached biofilms on molecular diffusion. We investigated the biodegradation by indigenous organisms of a set of 16 standard polycyclic aromatic hydrocarbons (PAHs) in coal tar contaminated soil from a manufactured gas plant site in Connecticut in well- mixed aerobic reactors containing various additives over a 93-106 day period. Parallel desorption experiments were conducted in the presence of a biocide and an excess of Tenax-TA adsorbent beads to simulate desorption to infinite dilution (i.e., maximal concentration gradient for diffusion). Both biotransformation and desorption decreased with PAH ring size, as expected. Biodegradation by native organisms was strongly accelerated by addition of inorganic nutrients (N, P, K, and trace metals). In the absence of added nutrients, the biodegradation resistant fraction correlated well with the desorption resistant fraction. However, in the presence of added nutrients, the extent of biodegradation was greater than the extent of desorption except for the largest compounds, which neither degraded nor desorbed. The ability of nutrients to accelerate degradation of bioavailable PAHs by native cells indicates that the persistence of PAHs for many decades at this site is likely due to nutrient-limited natural attenuation. The surprising result of this study is that application of nutrients promotes `facilitated bioavailability' of PAHs in this soil to indigenous microorganisms.

  10. Comparative metagenomic analysis of PAH degradation in soil by a mixed microbial consortium.

    PubMed

    Zafra, German; Taylor, Todd D; Absalón, Angel E; Cortés-Espinosa, Diana V

    2016-11-15

    In this study, we used a taxonomic and functional metagenomic approach to analyze some of the effects (e.g. displacement, permanence, disappearance) produced between native microbiota and a previously constructed Polycyclic Aromatic Hydrocarbon (PAH)-degrading microbial consortium during the bioremediation process of a soil polluted with PAHs. Bioaugmentation with a fungal-bacterial consortium and biostimulation of native microbiota using corn stover as texturizer produced appreciable changes in the microbial diversity of polluted soils, shifting native microbial communities in favor of degrading specific populations. Functional metagenomics showed changes in gene abundance suggesting a bias towards aromatic hydrocarbon and intermediary degradation pathways, which greatly favored PAH mineralization. In contrast, pathways favoring the formation of toxic intermediates such as cytochrome P450-mediated reactions were found to be significantly reduced in bioaugmented soils. PAH biodegradation in soil using the microbial consortium was faster and reached higher degradation values (84% after 30 d) as a result of an increased co-metabolic degradation when compared with other mixed microbial consortia. The main differences between inoculated and non-inoculated soils were observed in aromatic ring-hydroxylating dioxygenases, laccase, protocatechuate, salicylate and benzoate-degrading enzyme genes. Based on our results, we propose that several concurrent metabolic pathways are taking place in soils during PAH degradation. PMID:27484946

  11. Evaluation of PAH contamination in soil treated with solid by-products from shale pyrolysis.

    PubMed

    Nicolini, Jaqueline; Khan, Muhammad Y; Matsui, M; Côcco, Lílian C; Yamamoto, Carlos I; Lopes, Wilson A; de Andrade, Jailson B; Pillon, Clenio N; Arizaga, Gregorio G Carbajal; Mangrich, Antonio S

    2015-01-01

    The aim of this work was to evaluate the concentrations of polycyclic aromatic hydrocarbons (PAHs) in soils to which solid shale materials (SSMs) were added as soil conditioners. The SSMs were derived from the Petrosix pyrolysis process developed by Petrobras (Brazil). An improved ultrasonic agitation method was used to extract the PAHs from the solid samples (soils amended with SSMs), and the concentrations of the compounds were determined by gas chromatography coupled to mass spectrometry (GC-MS). The procedure provided satisfactory recoveries, detection limits, and quantification limits. The two-, three-, and four-ring PAHs were most prevalent, and the highest concentration was obtained for phenanthrene (978 ± 19 μg kg(-1) in a pyrolyzed shale sample). The use of phenanthrene/anthracene and fluoranthene/pyrene ratios revealed that the PAHs were derived from petrogenic rather than pyrogenic sources. The measured PAH concentrations did not exceed national or international limit values, suggesting that the use of SSMs as soil conditioners should not cause environmental damage. PMID:25399121

  12. In-situ Phytoremediation of PAH and PCB Contaminated Marine Sediments with Eelgrass (Zostera marina)

    SciTech Connect

    Huesemann, Michael H.; Hausmann, Tom S.; Fortman, Timothy J.; Thom, Ronald M.; Cullinan, Valerie I.

    2009-10-01

    In view of the fact that there are presently no cost-effective in-situ treatment technologies for contaminated sediments, a 60 week long phytoremediation feasibility study was conducted in seawater-supplied outdoor ponds to determine whether eelgrass (Zostera marina) is capable of removing polynuclear aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) from submerged marine sediments. It was determined that all PAHs and PCBs, independent of the number of aromatic rings and degree of chlorination, respectively, were removed to a much larger extent in planted sediments compared to unplanted controls. After 60 weeks of treatment, the concentration of total PAHs decreased by 73% in planted sediments but only 25% in unplanted controls. Similarly, total PCBs declined by 60% in the presence of plants while none were removed in the unplanted sediment. Overall, PAH and PCB biodegradation was greatest in the sediment layer that contained most of the eelgrass roots. Abiotic desorption tests conducted at week 32 confirmed that the phytoremediation process was not controlled by mass-transfer or bioavailability limitations since all PAHs and PCBs desorbed rapidly and to a large extent from the sediment. PAHs were detected in both roots and shoots, with root and shoot bioaccumulation factors for total PAHs amounting to approximately 3 and 1, respectively, after 60 weeks of phytoremediation treatment. Similarly, the root bioccumulation factor for total PCBs was around 4, while no PCBs were detected in the eelgrass leaves at the end of the experiment. The total mass fraction of PAHs and PCBs absorbed and translocated by plant biomass during the 60 week period was insignificant, amounting to less than 0.5% of the total mass of PAHs and PCBs which was initially present in the sediment. Finally, the number of total heterotrophic bacteria and hydrocarbon degraders was slightly but not statistically significantly greater in planted sediments than in unplanted controls

  13. Observing PAH Hydrogenation with Scanning Tunneling Microscopy

    NASA Astrophysics Data System (ADS)

    Cassidy, A. M.; Nilsson, L.; Balog, R.; Thrower, J.; Jorgensen, B.; Hornekaer, L.

    2011-05-01

    The interaction between thin films of polycyclic aromatic hydrocarbons (PAHs) and atomic H has been studied using scanning tunneling microscopy (STM). Observational evidence suggests that hydrogenated PAHs are located in regions of the interstellar medium (ISM) where there are high concentrations of molecular hydrogen (H2)1. It has previously been postulated that hydrogenated PAHs act as catalysts for the formation of H22. While many studies have focused on the role of ionic PAHs in the formation of H23, here we consider the role of neutral species. Neutral PAHs are expected to be stable and to condense on grain surfaces present in dense interstellar clouds, in regions of low UV flux4. PAH molecules were deposited in thin films under ultra high vacuum (UHV) conditions. Monolayer films were subsequently characterised using STM, at liquid N2 temperatures. The films were then exposed to thermally-cracked atomic H and were again characterised using STM. Contrast in the STM images showed submolecular changes to the electronic structure of the PAH molecules only after exposure to atomic H. This suggests the formation of superhydrogenated species. DFT calculations have predicted that such superhydrogenated species are stable and can act as catalysts for the formation of H2 through abstraction reactions5. Complimentary thermal desorption experiments support these findings.

  14. PAHs in the halo of NGC 5529

    NASA Astrophysics Data System (ADS)

    Irwin, J. A.; Kennedy, H.; Parkin, T.; Madden, S.

    2007-11-01

    We present sensitive ISO λ 6.7~μm observations of the edge-on galaxy, NGC 5529, finding an extensive MIR halo around NGC 5529. The emission is dominated by PAHs in this band. The PAH halo has an exponential scale height of 3.7 kpc but can still be detected as far as ≈10 kpc from the plane to the limits of the high dynamic range (1770/1) data. This is the most extensive PAH halo yet detected in a normal galaxy. This halo shows substructure and the PAHs likely originate from some type of disk outflow. PAHs are long-lived in a halo environment and therefore continuous replenishment from the disk is not required (unless halo PAHs are also being destroyed or removed), consistent with the current low SFR of the galaxy. The PAHs correlate spatially with halo Hα emission, previously observed by Miller & Veilleux (2003, ApJS, 148, 383); both components are likely excited/ionized by in-disk photons that are leaking into the halo. The presence of halo gas may be related to the environment of NGC 5529 which contains at least 17 galaxies in a small group of which NGC 5529 is the dominant member. Of these, we have identified two new companions from the SDSS.

  15. Sources appointment and ecological risk assessment of polycyclic aromatic hydrocarbons (PAHs) in sediments of Erhai Lake, a low-latitude and high-altitude lake in southwest China.

    PubMed

    Hezhong, Yuan; Enlou, Zhang; Qi, Lin; Rong, Wang; Enfeng, Liu

    2016-03-01

    Sixteen polycyclic aromatic hydrocarbons (PAHs) were analyzed from the surficial sediments in Erhai Lake, a plateau lake in China. The results showed that except for acenaphthylene (Ace) Ace and Dibenz(a,h)anthracene (DBA), the central region contained individual PAHs at concentrations lower than those in other lake regions. Total concentration of the PAHsPAHs) in the sediments from Erhai Lake ranged from 32.42 to 558.53 mg/kg with a mean value of 256.70 mg/kg. The maximum value of ΣPAHs was observed in the north region of the lake and more than 10-fold higher than the minimum values. Moreover, high molecular weight (HMW) PAHs, especially 5-ring PAHs, accounted for higher ratios up to 76 % relative to other PAHs compound in almost all sampling sites. Molecular diagnostic ratios including anthtacene (Ant)/(Ant + phenanthrene (Phe)), fluoranthene (Flt)/(Flt + pyrene (Pyr)), benz(a)anthracene (BaA)/(BaA + chrysene (Chr)), and indeno(1,2,3-cd)pyrene (IPY)/(IPY + benz(g,h,i)perylene (BPE)) were recorded at all sampling sites and indicated that the origin of PAHs in Erhai Lake was predominately pyrolytic. Furthermore, principal component analysis with component dominating by HMW PAHs showed that combustion origins were the primary contamination sources of PAHs in the sediments of Erhai Lake. Finally, ecological risk assessment indicated that the sediments from Erhai Lake are exposed to potential low risk for ΣPAHs, and the ecological risk decreases in the order of northern region > southern region > central region. PMID:26507728

  16. Diurnal and nocturnal measurements of PAH, nitro-PAH, and oxy-PAH compounds in atmospheric particulate matter of a sugar cane burning region

    NASA Astrophysics Data System (ADS)

    Souza, Kely F.; Carvalho, Lilian R. F.; Allen, Andrew G.; Cardoso, Arnaldo A.

    2014-02-01

    Polycyclic aromatic hydrocarbons (PAHs), nitro-PAHs, and oxy-PAHs were studied in the atmospheric particulate matter of a subtropical rural region (São Paulo State, Brazil) affected by emissions from sugar cane burning. Diurnal and nocturnal samples were collected from May to June of 2010. In general, average PAH concentrations were significantly higher at night, suggesting that the compounds were predominantly emitted to the atmosphere during biomass burning (which was mainly performed at night). The maximum average PAH concentration was found for benzo[b]fluoranthene at night (2.9 ± 5.4 ng m-3). Among the nitro-PAH compounds, the highest average concentrations were obtained for 9-nitrophenanthrene in diurnal and nocturnal samples (1.5 ± 1.2 and 1.3 ± 2.1 ng m-3, respectively). In contrast to the PAH and nitro-PAH compounds, the oxy-PAHs could not be directly associated with sugar cane burning. The most abundant oxy-PAH compound was benzanthrone (1.6 ± 1.3 ng m-3) at night, followed by 9,10-anthraquinone (1.1 ± 0.9 ng m-3) and 9-fluorenone (0.4 ± 0.1 ng m-3) during the day. A correlation matrix was used to explore the origins of the different compounds. The data suggested that during the daytime, direct emissions (mainly in vehicle exhaust) contributed to the presence of PAHs, nitro-PAHs, and oxy-PAHs in air. Photochemical production also appeared to be a source of the majority of nitro-PAHs and oxy-PAHs, while photolysis could have contributed to removal of the nitro-PAHs during the daytime. At night, sugar cane burning emissions were the primary source of the PAHs and nitro-PAHs, with additional sources also contributing to the levels of oxy-PAHs in the atmosphere.

  17. Urban sprawl leaves its PAH signature

    USGS Publications Warehouse

    Van Metre, P.C.; Mahler, B.J.; Furlong, E.T.

    2000-01-01

    The increasing vehicle traffic associated with urban sprawl in the United States is frequently linked to degradation of air quality, but its effect on aquatic sediment is less well-recognized. This study evaluates trends in PAHs, a group of contaminants with multiple urban sources, in sediment cores from 10 reservoirs and lakes in six U.S. metropolitan areas. The watersheds chosen represent a range in degree and age of urbanization. Concentrations of PAHs in all 10 reservoirs and lakes increased during the past 20-40 years. PAH contamination of the most recently deposited sediment at all sites exceeded sediment-quality guidelines established by Environment Canada, in some cases by several orders of magnitude. These results add a new chapter to the story told by previous coring studies that reported decreasing concentrations of PAHs after reaching highs in the 1950s. Concurrent with the increase in concentrations is a change in the assemblage of PAHs that indicates the increasing trends are driven by combustion sources. The increase in PAH concentrations tracks closely with increases in automobile use, even in watersheds that have not undergone substantial changes in urban land-use levels since the 1970s.The increasing vehicle traffic associated with urban sprawl in the United States is frequently linked to degradation of air quality, but its effect on aquatic sediment is less well-recognized. This study evaluates trends in PAHs, a group of contaminants with multiple urban sources, in sediment cores from 10 reservoirs and lakes in six U.S. metropolitan areas. The watersheds chosen represent a range in degree and age of urbanization. Concentrations of PAHs in all 10 reservoirs and lakes increased during the past 20-40 years. PAH contamination of the most recently deposited sediment at all sites exceeded sediment-quality guidelines established by Environment Canada, in some cases by several orders of magnitude. These results add a new chapter to the story told by

  18. Two-stage biotransformation of 2,4,6-trinitrotoluene

    SciTech Connect

    VanderLoop, S.L.; Suidan, M.T.; Moteleb, M.A.; Maloney, S.W.

    1995-12-31

    TNT is the explosive most widely used by the military, but current technologies for treating munitions production wastewater are costly and produce a secondary waste, spent GAC. Bioremediation holds promise as a more effective and less costly treatment strategy. An anaerobic fluidized-bed granular activated carbon (GAC) bioreactor in series with an activated sludge reactor was used to treat 2,4,6-trinitrotoluene (TNT). A wastewater solution of 100 mg/L 2,4,6-TNT, as well as carbonate buffer and nutrient solutions, were fed to the anaerobic reactor. Ethanol and ammonia were supplied for microbial growth at 540 mg/L and 20 mg/L, respectively. The mixed anaerobic culture completely transformed the TNT to unknown products. Attempts to detect these products by gas chromatography (GC) and high-performance liquid chromatography (HPLC) were unsuccessful. The effluent from this reactor was treated further in an activated sludge system. The TNT transformation products were partially oxidized in the aerobic stage, resulting in recovery of 91% of the total influent nitrogen as ammonia, nitrate, and biomass. This corresponds to recovery of 82% of influent TNT nitrogen.

  19. A multivariate receptor modeling study of air-borne particulate PAHs: Regional contributions in a roadside environment.

    PubMed

    Kim, Bong Mann; Lee, Seung-Bok; Kim, Jin Young; Kim, Sunwha; Seo, Jihoon; Bae, Gwi-Nam; Lee, Ji Yi

    2016-02-01

    Understanding the geographic source contributions by particulate polycyclic aromatic hydrocarbons (PAHs) is important for the Korean peninsula due to its downwind location from source areas. Regional influence of particulate PAHs was previously identified using diagnostic ratios applied to mobile source dominated roadside sampling data (Kim et al., 2012b). However, no study has yet been conducted to quantify the regional source contributions. We applied a multivariate receptor modeling tool to identify and quantify the regional source contributions to particulate PAHs in Seoul. Sampling of roadside particulate PAHs was conducted in Seoul, Korea for four years between May 2005 and April 2009, and data analysis was performed with a new multivariate receptor model, Solver for Mixture Problem (SMP). The SMP model identified two sources, local mobile source and transported regional source, and quantified their source contributions. Analysis of the particulate PAHs data reveals three types of episodic periods: a high regional source contribution period with one case, a high mobile source contribution period with three cases, and a normal contribution period with eight cases. Four-year average particulate PAHs source contributions from the two sources are 4.6 ng m(-3) and 10.7 ng m(-3) for regional and mobile sources, respectively and equivalent to 30% and 70% of the total estimated contribution from each of these sources. PMID:26473551

  20. Planetary Rings

    NASA Astrophysics Data System (ADS)

    Gordon, M. K.; Araki, S.; Black, G. J.; Bosh, A. S.; Brahic, A.; Brooks, S. M.; Charnoz, S.; Colwell, J. E.; Cuzzi, J. N.; Dones, L.; Durisen, R. H.; Esposito, L. W.; Ferrari, C.; Festou, M.; French, R. G.; Giuliatti-Winter, S. M.; Graps, A. L.; Hamilton, D. P.; Horanyi, M.; Karjalainen, R. M.; Krivov, A. V.; Krueger, H.; Larson, S. M.; Levison, H. F.; Lewis, M. C.; Lissauer, J. J.; Murray, C. D.; Namouni, F.; Nicholson, P. D.; Olkin, C. B.; Poulet, F.; Rappaport, N. J.; Salo, H. J.; Schmidt, J.; Showalter, M. R.; Spahn, F.; Spilker, L. J.; Srama, R.; Stewart, G. R.; Yanamandra-Fisher, P.

    2002-08-01

    The past two decades have witnessed dramatic changes in our view and understanding of planetary rings. We now know that each of the giant planets in the Solar System possesses a complex and unique ring system. Recent studies have identified complex gravitational interactions between the rings and their retinues of attendant satellites. Among the four known ring systems, we see elegant examples of Lindblad and corotation resonances (first invoked in the context of galactic disks), electromagnetic resonances, spiral density waves and bending waves, narrow ringlets which exhibit internal modes due to collective instabilities, sharp-edged gaps maintained via tidal torques from embedded moonlets, and tenuous dust belts created by meteoroid impact onto, or collisions between, parent bodies. Yet, as far as we have come, our understanding is far from complete. The fundamental questions confronting ring scientists at the beginning of the twenty-first century are those regarding the origin, age and evolution of the various ring systems, in the broadest context. Understanding the origin and age requires us to know the current ring properties, and to understand the dominant evolutionary processes and how they influence ring properties. Here we discuss a prioritized list of the key questions, the answers to which would provide the greatest improvement in our understanding of planetary rings. We then outline the initiatives, missions, and other supporting activities needed to address those questions, and recommend priorities for the coming decade in planetary ring science.

  1. PAH in the laboratory and interstellar space

    NASA Technical Reports Server (NTRS)

    Wdowiak, Thomas J.; Flickinger, Gregory C.; Boyd, David A.

    1989-01-01

    The theory that polycyclic aromatic hydrocarbons (PAHs) are a constituent of the interstellar medium, and a source of the IR emission bands at 3.3, 6.2, 7.7, 8.6, and 11.3 microns is being studied using PAH containing acid insoluble residue of the Orgueil CI meteorite and coal tar. FTIR spectra of Orgueil PAH material that has undergone thermal treatment, and a solvent insoluble fraction of coal tar that has been exposed to hydrogen plasma are presented. The UV excided luminescence spectrum of a solvent soluble coal tar film is also shown. Comparison of the lab measurements with observations appears to support the interstellar PAH theory, and shows the process of dehydrogenation expected to take place in the interstellar medium.

  2. SOURCES OF HUMAN EXPOSURE TO AIRBORNE PAH

    EPA Science Inventory

    Personal exposures to airborne particulate polycyclic aromatic hydrocarbons (PAHs) were studied in several populations in the US, Japan, and Czech Republic. Personal exposure monitors, developed for human exposure biomonitoring studies were used to collect fine particles (<_ 1....

  3. Amphibian responses to photoinduced toxicity of PAHs

    SciTech Connect

    Hatch, A.C.; Burton, G.A. Jr.

    1995-12-31

    Amphibians are essential components of many ecosystems, yet little information exists on their sensitivity to environmental stressors. Recent evidence shows amphibian diversity is declining. Others have suggested this decline is a result of increasing ultraviolet (UV) light levels. Polycyclic aromatic hydrocarbons (PAHs) are widespread pollutants in the aquatic environment and their toxicity is increased in the presence of UV light. Embryos of two frogs (Rana pipiens and Xenopus laevis) were exposed to a PAH, fluoranthene, to evaluate amphibian responses to this common contaminant in the presence of sunlight. Hatching rate and development were measured in field and laboratory exposures at multiple concentrations and varying UV intensities. Hatching rate was relatively unaffected, while newly hatched larvae were sensitive to low (ug/L) concentrations. Response was related to both PAH concentration and UV intensity. Results suggest that PAH contamination in the aquatic environment may contribute to declines in amphibian populations.

  4. Metabolomic analysis to define and compare the effects of PAHs and oxygenated PAHs in developing zebrafish

    PubMed Central

    Elie, Marc R.; Choi, Jaewoo; Nkrumah-Elie, Yasmeen M.; Gonnerman, Gregory D.; Stevens, Jan F.; Tanguay, Robert L.

    2015-01-01

    Polycyclic aromatic hydrocarbons (PAHs) and their oxygenated derivatives are ubiquitously present in diesel exhaust, atmospheric particulate matter and soils sampled in urban areas. Therefore, inhalation or non-dietary ingestion of both PAHs and oxy-PAHs are major routes of exposure for people; especially young children living in these localities. While there has been extensive research on the parent PAHs, limited studies exist on the biological effects of oxy-PAHs which have been shown to be more soluble and more mobile in the environment. Additionally, investigations comparing the metabolic responses resulting from parent PAHs and oxy-PAHs exposures have not been reported. To address these current gaps, an untargeted metabolomics approach was conducted to examine the in vivo metabolomic profiles of developing zebrafish (Danio rerio) exposed to 4 µM of benz[a]anthracene (BAA) or benz[a]anthracene-7, 12-dione (BAQ). By integrating multivariate, univariate and pathway analyses, a total of 62 metabolites were significantly altered after 5 days of exposure. The marked perturbations revealed that both BAA and BAQ affect protein biosynthesis, mitochondrial function, neural development, vascular development and cardiac function. Our previous transcriptomic and genomic data were incorporated in this metabolomics study to provide a more comprehensive view of the relationship between PAH and oxy-PAH exposures on vertebrate development. PMID:26001975

  5. Metabolomic analysis to define and compare the effects of PAHs and oxygenated PAHs in developing zebrafish.

    PubMed

    Elie, Marc R; Choi, Jaewoo; Nkrumah-Elie, Yasmeen M; Gonnerman, Gregory D; Stevens, Jan F; Tanguay, Robert L

    2015-07-01

    Polycyclic aromatic hydrocarbons (PAHs) and their oxygenated derivatives are ubiquitously present in diesel exhaust, atmospheric particulate matter and soils sampled in urban areas. Therefore, inhalation or non-dietary ingestion of both PAHs and oxy-PAHs are major routes of exposure for people; especially young children living in these localities. While there has been extensive research on the parent PAHs, limited studies exist on the biological effects of oxy-PAHs which have been shown to be more soluble and more mobile in the environment. Additionally, investigations comparing the metabolic responses resulting from parent PAHs and oxy-PAHs exposures have not been reported. To address these current gaps, an untargeted metabolomics approach was conducted to examine the in vivo metabolomic profiles of developing zebrafish (Danio rerio) exposed to 4 µM of benz[a]anthracene (BAA) or benz[a]anthracene-7,12-dione (BAQ). By integrating multivariate, univariate and pathway analyses, a total of 63 metabolites were significantly altered after 5 days of exposure. The marked perturbations revealed that both BAA and BAQ affect protein biosynthesis, mitochondrial function, neural development, vascular development and cardiac function. Our previous transcriptomic and genomic data were incorporated in this metabolomics study to provide a more comprehensive view of the relationship between PAH and oxy-PAH exposures on vertebrate development. PMID:26001975

  6. Solubilization of PAH mixtures by three different anionic surfactants.

    PubMed

    Chun, Chan Lan; Lee, Jung-Ju; Park, Jae-Woo

    2002-01-01

    Solubilization of naphthalene and phenanthrene into the micelles formed by three different anionic surfactants was investigated for single, binary, and ternary mixtures including pyrene. The three surfactants were sodium dodecylbenzene sulfonate (SDDBS), monoalkylated disulfonated diphenyl oxide (MADS-C12), and dialkylated disulfonated diphenyl oxide (DADS-C12). The order of increasing solubility enhancement of naphthalene and phenanthrene was SDDBS < MADS-C12 < < DADS-C12, which indicates that the hydrophobic chains in micellar core play more important role for the solubilization of polycyclic aromatic hydrocarbons (PAHs) than the benzene rings in palisade layer of a micelle. The solubility enhancement of naphthalene was slightly changed in PAH mixtures. The solubility of phenanthrene was greatly enhanced in presence of naphthalene but reduced in presence of pyrene. The explanation for these results could be that less hydrophobic compounds can be solubilized at the interfacial region of a hydrophobic core, which reduces the interfacial tension between the core and water, and then the reduced interfacial tension can support a larger core volume for the same interfacial energy. PMID:12009127

  7. Two new polytypes of 2,4,6-tri­bromo­benzo­nitrile

    PubMed Central

    Britton, Doyle; Noland, Wayland E.; Tritch, Kenneth J.

    2016-01-01

    Three polymorphs of 2,4,6-tri­bromo­benzo­nitrile (RCN), C7H2Br3N, two of which are novel and one of which is a redetermination of the original structure first determined by Carter & Britton [(1972). Acta Cryst. B28, 945–950] are found to be polytypic. Each has a layer structure which differs only in the stacking of the layers. Each layer is composed of mol­ecules associated through C N⋯Br contacts which form R 2 2(10) rings. Two such rings are associated with each N atom; one with each ortho-Br atom. No new polytypes of 1,3,5-tri­bromo-2-iso­cyano­benzene (RNC) were found but a re-determination of the original structure by Carter et al. [(1977). Cryst. Struct. Commun. 6, 543–548] is presented. RNC was found to be isostructural with one of the novel polytypes of RCN. Unit cells were determined for 23 RCN samples and 11 RNC samples. Polytypes could not be distinguished based on crystal habits. In all four structures, each mol­ecule of the asymmetric unit lies across a mirror plane. PMID:26958382

  8. 4,6-Dimethyl-pyrimidin-2-amine.

    PubMed

    Fu, Wei-Wei; Liu, Yang; Huang, Geng; Zhu, Xiao-Ming

    2013-01-01

    The asymmetric unit of the title compound, C6H9N3, contains three crystallographically independent mol-ecules of similar geometry. All of the mol-ecules are almost planar, with r.m.s. deviations of 0.003, 0.016 and 0.005 Å. In the crystal, the mol-ecules are linked by N-H⋯N hydrogen bonds into zigzag ribbons parallel to the c axis, generating rings of R2(2)(8) graph-set motif. PMID:23476420

  9. Laboratory Studies of Interstellar PAH Analogs

    NASA Technical Reports Server (NTRS)

    Salama, Farid; DeVincenzi, Donald (Technical Monitor)

    2000-01-01

    Polycyclic aromatic hydrocarbons (PAHs) are now considered to be an important and ubiquitous component of the organic material in space. PAHs are found in a large variety of extraterrestrial materials such as interplanetary dust particles (IDPs) and meteoritic materials. PAHs are also good candidates to account for the infrared emission bands (UIRs) and the diffuse interstellar optical absorption bands (DIBs) detected in various regions of the interstellar medium. The recent observations made with the Infrared Space Observatory (ISO) have confirmed the ubiquitous nature of the UIR bands and their carriers. PAHs are though to form through chemical reactions in the outflow from carbon-rich stars in a process similar to soot formation. Once injected in the interstellar medium, PAHs are further processed by the interstellar radiation field, interstellar shocks and energetic particles. A major, dedicated, laboratory effort has been undertaken over the past years to measure the physical and chemical characteristics of these complex molecules and their ions under experimental conditions that mimic the interstellar conditions. These measurements require collision-free conditions where the molecules and ions are cold and chemically isolated. The spectroscopy of PAHs under controlled conditions represents an essential diagnostic tool to study the evolution of extraterrestrial PAHs. The Astrochemistry Laboratory program will be discussed through its multiple aspects: objectives, approach and techniques adopted, adaptability to the nature of the problem(s), results and implications for astronomy as well as for molecular spectroscopy. A review of the data generated through laboratory simulations of space environments and the role these data have played in our current understanding of the properties of interstellar PAHs will be presented. The discussion will also introduce the newest generation of laboratory experiments that are currently being developed in order to provide a

  10. Molecular Spectroscopy in Astrophysics: Interstellar PAHs

    NASA Technical Reports Server (NTRS)

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

    2000-01-01

    Polycyclic aromatic hydrocarbons (PAHs) are now considered to be an important and ubiquitous component of the organic material in space. PAHs are found in a large variety of extraterrestrial materials such as interplanetary dust particles (IDPs) and meteoritic materials. PAHs are also good candidates to account for the infrared emission bands (UIRs) and the diffuse interstellar optical absorption bands (DIBs) detected in various regions of the interstellar medium. The recent observations made with the Infrared Space Observatory (ISO) have confirmed the ubiquitous nature of the UIR bands and their carriers. PAHs are thought to form through chemical reactions in the outflow from carbon-rich stars in a process similar to soot formation. Once injected in the interstellar medium, PAHs are further processed by the interstellar radiation field, interstellar shocks and energetic particles. A long-term laboratory effort has been undertaken to measure the physical and chemical characteristics of these carbon molecules and their ions under experimental conditions that mimic the interstellar conditions. These measurements require collision-free conditions where the molecules and ions are cold and chemically isolated. The spectroscopy of PAHs under controlled conditions represents an essential diagnostic tool to study the evolution of extraterrestrial PAHs. The laboratory results will be discussed as well as the implications for astronomy and for molecular spectroscopy. A review of the data generated through laboratory simulations of space environments and the role these data have played in our current understanding of the properties of interstellar PAHs will be presented. We will also present the new generation of laboratory experiments that are currently being developed in order to provide a closer simulation of space environments and a better support to space missions.

  11. Indoor/outdoor relationships and diurnal/nocturnal variations in water-soluble ion and PAH concentrations in the atmospheric PM2.5 of a business office area in Jinan, a heavily polluted city in China

    NASA Astrophysics Data System (ADS)

    Zhu, Yanhong; Yang, Lingxiao; Meng, Chuanping; Yuan, Qi; Yan, Chao; Dong, Can; Sui, Xiao; Yao, Lan; Yang, Fei; Lu, Yaling; Wang, Wenxing

    2015-02-01

    Indoor/outdoor and diurnal/nocturnal variations in PM2.5 and associated water-soluble ions and polycyclic aromatic hydrocarbons (PAHs) were examined in a business office during the summer and autumn of 2010 in Jinan, China. Both indoor and outdoor PM2.5 levels were higher than the value recommended by the WHO, and outdoor sources were found to be the major contributors to indoor PM2.5. SO42-, NO3- and NH4+ were the dominant water-soluble ions in both indoor and outdoor particles. During daytime, NO3- mainly came from indoor sources, which was related to the temperature difference between the indoor and outdoor air. During daytime, the 15 monitored PAHs were all largely from indoor sources, while during nighttime, the 3 -4-ring PAHs were mainly generated indoors and the 5-6-ring PAHs predominantly came from the outdoor air. The diurnal/nocturnal variations of PAHs suggested that gas/particle partitioning driven by temperature makes a significant contribution to the variation in PAH concentrations. The diagnostic ratios revealed that biomass burning had an important contribution to outdoor PAH concentrations in autumn. The results of a risk assessment of PAH pollution suggested that indoor PAHs present more carcinogenic and mutagenic risks during daytime. Our results indicated that serious indoor air pollution in a business office presents a high health risk for workers.

  12. Polycyclic aromatic hydrocarbons (PAHs) in atmospheric PM2.5 and PM10 at a coal-based industrial city: Implication for PAH control at industrial agglomeration regions, China

    NASA Astrophysics Data System (ADS)

    Wu, Di; Wang, Zongshuang; Chen, Jianhua; Kong, Shaofei; Fu, Xiao; Deng, Hongbing; Shao, Guofan; Wu, Gang

    2014-11-01

    Eighteen polycyclic aromatic hydrocarbons (PAHs) in PM2.5 and PM10 are identified and quantified at five sites of E'erduosi in 2005 by GC-MS. Total PAH concentrations in PM2.5 and PM10 are in the ranges of 0.58-145.01 ng m- 3 and 5.80-180.32 ng m- 3 for the five sites, decreasing as coal-chemical base site (ZGE) > heavy industrial site (QPJ) > residential site with heavy traffic (DS) > suburban site surrounded by grassland (HJQ) > background site (QGN) for both PM2.5 and PM10. PAH concentrations in the coal-chemical base site are 250 and 31.1 times of those in the background site. Flu, Pyr, Chr, BbF, BeP, IND and BghiP are abundant for the coal-chemical base site, totally accounting for 75% of the PAH concentrations. 4, 5 and 6 rings PAHs are dominant, accounting for 88.9-94.2% and 90.5-94.1% of PAHs in PM2.5 and PM10, respectively. Combustion-derived PAH concentrations cover 42%-84% and 75%-82% of PAHs in PM2.5 and PM10, indicating large amounts of combustion sources existed for them in E'erduosi. PAH compositions between PM2.5 and PM10 are quite different from each other for sites with few human activities (HJQ and QGN) by coefficient of divergence analysis. Results obtained from principal component analysis and diagnostic ratios indicate that coal combustion, vehicle emission, wood combustion and industrial processes are the main sources for PAHs in E'erduosi. According to BaP equivalent concentration, the potential health risk of PAHs in PM2.5 at the two industrial sites ZGE and QPJ are 537 and 460 times of those for the background site. And they are 4.3 and 3.7 times of those for the residential site. The potential PAH pollution in particles at other industrial agglomeration regions that occurred in China in recent years should be paid attention by the local government.

  13. Far-ir Pah Spectroscopy And The Identification Of An Individual Astronomical Pah Molecule

    NASA Astrophysics Data System (ADS)

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

    2010-05-01

    Polycyclic Aromatic Hydrocarbons (PAHs) are widespread across the Universe and influence many stages of the Galactic lifecycle. The presence of PAHs has been well established and the rich mid-IR PAH spectrum is now commonly used as a probe into inter(stellar) environments. With a new spectral window opening up in the far-IR, the quest for identifying a unique member of the interstellar PAH family has begun. To guide this search, the far-IR (> 20 μm) spectra of different sets of PAHs are investigated using the NASA Ames PAH IR Spectroscopic Database - a large coherent set (> 600 spectra) of laboratory measured and DFT computed infrared spectra of PAHs from C10H8 to C130H28. These sets explore the influence of size, shape, charge and composition on the far-IR PAH spectrum. The far-IR is the domain of the so- called `drumhead’ modes and other molecular vibrations involving low order bending vibrations of the carbon skeleton as a whole. As for drums, these modes are considered to be very molecule and shape specific and promise to be a key diagnostic for specific PAHs. Here, the sensitivity of these `drumhead’ modes to size and shape is assessed by comparing the frequencies of the lowest drumhead modes of a family of circular shaped (the coronene `family') and rhombus shaped (the pyrene `family') PAH molecules. From the study of the far-IR PAH spectra of different sets as well as from the analysis of the `drumhead’ modes, some suggestions for an observing strategy are made.

  14. 4,6-Dihy­droxy-4,6-dimethyl-1,3-diazinane-2-thione

    PubMed Central

    Aliyeva, Khatira N.; Maharramov, Abel M.; Allahverdiyev, Mirze A.; Gurbanov, Atash V.; Brito, Iván

    2011-01-01

    In the title compound, C6H12N2O2S, the heterocyclic ring has a sofa conformation. The mol­ecular conformation is stabilized by an intra­molecular O—H⋯O hydrogen-bond inter­action with graph-set motif S(6). In the crystal, mol­ecules are linked by O—H⋯S, N—H⋯S and N—H⋯O hydrogen-bond inter­actions, forming an extended two-dimensional framework parallel to the ac plane. PMID:22058933

  15. Infrared spectra of interstellar deuteronated PAHs

    NASA Astrophysics Data System (ADS)

    Buragohain, Mridusmita; Pathak, Amit; Sarre, Peter

    2015-08-01

    Polycyclic Aromatic Hydrocarbon (PAH) molecules have emerged as a potential constituent of the ISM that emit strong features at 3.3, 6.2, 7.7, 8.6, 11.2 and 12.7 μm with weaker and blended features in the 3-20μm region. These features are proposed to arise from the vibrational relaxation of PAH molecules on absorption of background UV photons (Tielens 2008). These IR features have been observed towards almost all types of astronomical objects; say H II regions, photodissociation regions, reflection nebulae, planetary nebulae, young star forming regions, external galaxies, etc. A recent observation has proposed that interstellar PAHs are major reservoir for interstellar deuterium (D) (Peeters et al. 2004). According to the `deuterium depletion model' as suggested by Draine (2006), some of the Ds formed in the big bang are depleted in PAHs, which can account for the present value of D/H in the ISM. Hence, study of deuterated PAHs (PADs) is essential in order to measure D/H in the ISM.In this work, we consider another probable category of the large PAH family, i.e. Deuteronated PAHs (DPAH+). Onaka et al. have proposed a D/H ratio which is an order of magnitude smaller than the proposed value of D/H by Draine suggesting that if Ds are depleted in PAHs, they might be accommodated in large PAHs (Onaka et al. 2014). This work reports a `Density Functional Theory' calculation of large deuteronated PAHs (coronene, ovalene, circumcoronene and circumcircumcoronene) to determine the expected region of emission features and to find a D/H ratio that is comparable to the observational results. We present a detailed analysis of the IR spectra of these molecules and discuss the possible astrophysical implications.ReferencesDraine B. T. 2006, in ASP Conf. Ser. 348, Proc. Astrophysics in the Far Ultraviolet: Five Years of Discovery with FUSE, ed. G. Sonneborn, H. Moos, B-G Andersson (San Francisco, CA:ASP) 58Onaka T., Mori T. I., Sakon I., Ohsawa R., Kaneda H., Okada Y., Tanaka M

  16. Occurrence of polycyclic aromatic hydrocarbons (PAHs) in mussel (Mytilus galloprovincialis) and eel (Anguilla anguilla) from Bizerte lagoon, Tunisia, and associated human health risk assessment

    NASA Astrophysics Data System (ADS)

    Barhoumi, Badreddine; El Megdiche, Yassine; Clérandeau, Christelle; Ameur, Walid Ben; Mekni, Sabrine; Bouabdallah, Sondes; Derouiche, Abdelkader; Touil, Soufiane; Cachot, Jérôme; Driss, Mohamed Ridha

    2016-08-01

    The aim of this study is to measure PAHs concentrations in mussels (Mytilus galloprovincialis) and fish (Anguilla anguilla) from the Bizerte lagoon (north Tunisia), and evaluate their distribution and sources, in order to provide a baseline of the state of PAH contamination in this lagoon and assess their human health risk. For this purpose, several native mussel and fish specimens were collected and analyzed using a high-performance liquid chromatography method with fluorescence detection for 15 EPA priority PAHs. PAHs levels in mussels and fish ranged from 107.4 to 430.7 ng g-1 dw and 114.5-133.7 ng g-1 dw, respectively. Naphthalene was the major component measured in mussels (31.5-272.6 ng g-1 dw) and fish (57.9-68.6 ng g-1 dw) and all specimens were classified as moderately contaminated. The PAHs composition pattern was similar for both species and was dominated by the presence of PAHs with 2- to 3-rings. The study of PAH ratios indicated a mixed petrogenic/pyrolytic origin. The health risks by consumption of these species was assessed and showed to present no threat to public health concerning PAH intakes. The results of this study would provide a useful aid for sustainable marine management in the region.

  17. Planetary Rings

    NASA Technical Reports Server (NTRS)

    Cuzzi, Jeffrey N.

    1994-01-01

    Just over two decades ago, Jim Pollack made a critical contribution to our understanding of planetary ring particle properties, and resolved a major apparent paradox between radar reflection and radio emission observations. At the time, particle properties were about all there were to study about planetary rings, and the fundamental questions were, why is Saturn the only planet with rings, how big are the particles, and what are they made of? Since then, we have received an avalanche of observations of planetary ring systems, both from spacecraft and from Earth. Meanwhile, we have seen steady progress in our understanding of the myriad ways in which gravity, fluid and statistical mechanics, and electromagnetism can combine to shape the distribution of the submicron-to-several-meter size particles which comprise ring systems into the complex webs of structure that we now know them to display. Insights gained from studies of these giant dynamical analogs have carried over into improved understanding of the formation of the planets themselves from particle disks, a subject very close to Jim's heart. The now-complete reconnaissance of the gas giant planets by spacecraft has revealed that ring systems are invariably found in association with families of regular satellites, and there is ark emerging perspective that they are not only physically but causally linked. There is also mounting evidence that many features or aspects of all planetary ring systems, if not the ring systems themselves, are considerably younger than the solar system

  18. Spectroscopy of Jet-Cooled Neutral and Ionized PAHs: Implications for Interstellar Dust

    NASA Technical Reports Server (NTRS)

    Salama, F.; Tan, X.; Biennier, L.; Cami, J.

    2005-01-01

    We present the gas-phase spectroscopy of neutral and ionized polycyclic aromatic hydrocarbons (PAHs) measured in the W-Visible-NIR range in an astrophysically relevant environment. These measurements provide data on PAHs and nanometer sized particles that can now be directly compared to astronomical observations. The harsh physical conditions of the IS medium - characterized by a low temperature, an absence of collisions and strong VUV radiation fields - are simulated in the laborat'ory by associating a molecular beam with an ionizing discharge to generate a cold plasma expansion. PAH ions are formed from the neutral precursors in an isolated environment at low temperature ($\\sim lOO$-K). The spectra of neutral and ionized PAHs are measured using the high sensitivity methods of cavity ring down spectroscopy (CRDS) and multiplex integrated cavity output spectroscopy (MICOS). These experiments provide unique information on the spectra of free, cold large carbon molecules and ions in the gas phase. The electronic bands measured for ionized PAH are found to be intrinsically broad ($\\geq$20 cm$^{-l}$) while the bands associated with the neutral precursors are narrower (of the order of 2 - 10 cm$^{-l}$). The laboratory data are discussed and compared with recent astronomical spectra of large and narrow DIBs and with the spectra of circumstellar environments of selected carbon stars (see contribution of Cami et al.) and the implications for the interstellar PAH population are derived. Preliminary results also show that carbon nanoparticles are formed during the short residence time of the precursors in the plasma. This finding holds great potential for understanding the formation process of interstellar grains.

  19. Modulated gap junctional intercellular communication as a biomarker of PAH epigenetic toxicity: structure-function relationship.

    PubMed Central

    Upham, B L; Weis, L M; Trosko, J E

    1998-01-01

    Cancer is a multistage multimechanism process involving gene and/or chromosomal mutations (genotoxic events), altered gene expression at the transcriptional, translational, and post-translational levels (epigenetic events), and altered cell survival (proliferation and apoptosis or necrosis), resulting in an imbalance of the organism's homeostasis. Maintenance of the organism's homeostasis depends on the intricate coordination of genetic and metabolic events between cells via extracellular and intercellular communication mechanisms. The release of a quiescent cell, whether normal or premalignant, from the suppressing effects of communicating neighbors requires the downregulation of intercellular communication via gap junctions, thereby allowing factors that control intracellular events to exceed a critical mass necessary for the cell to either proliferate or undergo apoptosis. Therefore, determining the role an environmental pollutant must play in the multistage carcinogenic process includes mechanisms of epigenetic toxicity such as the effects of a compound on gap junctional intercellular communication (GJIC). A classic example of a class of compounds in which determination of carcinogenicity focused on genotoxic events and ignored epigenetic events is polycyclic aromatic hydrocarbons (PAHs). The study of structure-activity relationships of PAHs has focused exclusively on the genotoxic and tumor-initiating properties of the compound. We report on the structure-activity relationships of two- to four-ringed PAHs on GJIC in a rat liver epithelial cell line. PAHs containing a bay or baylike region were more potent inhibitors of GJIC than the linear PAHs that do not contain these regions. These are some of the first studies of determine the epigenetic toxicity of PAHs at the epigenetic level. Images Figure 1 PMID:9703481

  20. Solubility of 2,4,6-trinitrotoluene (TNT) in water

    SciTech Connect

    Ro, K.S.; Venugopal, A.; Adrian, D.D.; Constant, D.; Valsaraj, K.T.; Thibodeaux, L.J.; Qaisi, K.; Roy, D.

    1996-07-01

    Current literature values of 2,4,6-trinitrotoluene (TNT) solubility in water vary widely from 100 to 200 mg/L at room temperature. The authors investigated the effects of temperature and pH on the solubility of both reference TNT and field neat TNT obtained from the Alabama Army Ammunition Plant (AAAP), Childersburg, AL. The TNT solubility determined from this study was significantly lower than that of Taylor and Rinkenbach, which was cited by several reference chemical handbooks and articles. However, the values reported by the Merck Index and the Lange`s Handbook of Chemistry compared well with the authors` values. TNT solubility dropped rapidly as the pH increased. Three unknown HPLC peaks were observed at high pH, indicating a possibility of forming unknown transformation products. Both reference and field neat TNT solubility agreed well. A semiempirical solubility correlation was developed to predict the solubility of TNT at a temperature range from 6 C to 42 C.

  1. Determination of some carcinogenic PAHs with toxic equivalency factor along roadside soil within a fast developing northern city of India

    NASA Astrophysics Data System (ADS)

    Kumar, A. Vaneet; Kothiyal, N. C.; Kumari, Saruchi; Mehra, R.; Parkash, A.; Sinha, R. R.; Tayagi, S. K.; Gaba, R.

    2014-04-01

    The objective of the present study was to ascertain contamination levels, distribution behaviour and PAHs exposure during summer, winter and autumn during 2011-2012 in one of the developing cities of northern India. Average PAHs concentration was found to be 18.17, 4.04 and 16.38 μg g -1, whereas, concentration of 16 individual PAHs was found to vary between 0.02 and 200.23, 0.008 and 28.4 μg g -1, and 0.01 and 252.55 μg g -1 during summer, winter and autumn seasons, respectively. The average concentration of low and high carcinogenic PAHs during summer, winter and autumn was found to be 5.1 and 31.29, 2.1 and 6.4, 4.74 and 35.08 μg g -1 at most intercepts. The average ratio of low to high carcinogenic PAHs was found to be 1:6, 1:3, 1:7.6 during summer, winter and autumn, respectively. Five ringed PAHs were found in higher concentration in all seasons. Dib(ah)A and B(a)P were the two individual PAHs found in highest concentration during summer, winter and autumn seasons. Two tailed T-test was applied for authenticity of the results. Toxic equivalency factor of B(a)P and Dib(ah)A was maximum as compared to other PAHs. The study could be of great significance for the planners while considering environmental remedial measures.

  2. Toxicological studies on 2,4,6-tribromoanisole.

    PubMed

    Koschier, F; Gallo, M A; Feng, X; Baxter, G E; Preston, R; Stevens, K; Powers, W

    2011-09-01

    TBA, or 2,4,6-tribromoanisole, is a musty-smelling metabolite of 2,4,6-tribromophenol that is used as a flame retardant and an antifungal agent for wooden pallets and packaging materials. The compound can impart its peculiar, often offensive, odor on product packaging to the concern of consumers for the safety of the package contents. These studies were conducted to evaluate the safety of TBA to humans ingesting products tainted with TBA. In addition to the 28-day oral study, a bacterial reverse mutation study was conducted, and confirmed that TBA was not mutagenic. To evaluate oral safety, TBA was evaluated in single dose and 5-day and 4-week repeated dose oral toxicity studies in rats. The test article, administered in single gavage doses of 2000, 5000 and 7500 mg/kg body weight (bw), in 5 daily repeated doses of 1000, 2000 or 3000 mg/kg bw/day or in 28 daily oral gavage doses of 0 001, 0.01, 100, and 1000 mg/kg bw/day did not result in any deaths. Also, the single and repeat dose studies resulted in no significant differences between control and treated groups on body weight gain, food consumption, clinical observations, blood biochemical values, and hematology findings. Treatment-related adverse findings were only detected in male rats during repeated dose studies and were associated with high plasma concentrations of TBA. The test article-related finding of hyaline droplets in the cortical tubular epithelium of kidneys was associated with increases in α(2 μ)-globulin content in the kidneys as indicated by the intensity of immunohistochemical staining. These findings were correlated with an increased weight of kidneys in males administered 1000mg/kgbw/day for 28days. Chemical induction of hyaline droplets containing α(2μ)-globulin in the renal proximal tubule is a process unique to the male rat and is not relevant for human risk assessment. Findings of increased liver weight with minimal centrilobular to diffuse hepatocellular hypertrophy in males treated

  3. Development of eukaryotic zoospores within polycyclic aromatic hydrocarbon (PAH)-polluted environments: a set of behaviors that are relevant for bioremediation.

    PubMed

    Sungthong, Rungroch; van West, Pieter; Cantos, Manuel; Ortega-Calvo, Jose Julio

    2015-04-01

    In this study, we assessed the development (formation, taxis and settlement) of eukaryotic zoospores under different regimes of exposure to polycyclic aromatic hydrocarbons (PAHs), which imitated environmental scenarios of pollution and bioremediation. With this aim, we used an oomycete, Pythium aphanidermatum, as a source of zoospores and two PAH-degrading bacteria (Mycobacterium gilvum VM552 and Pseudomonas putida G7). The oomycete and both bacteria were not antagonistic, and zoospore formation was diminished only in the presence of the highest bacterial cell density (10(8)-10(10) colony-forming units mL(-1)). A negative influence of PAHs on zoospore formation and taxis was observed when PAHs were exposed in combination with organic solutions and polar solvents. Co-exposure of PAHs with non-polar solvents [hexadecane (HD) and 2,2,4,4,6,8,8-heptamethylnonane (HMN)] did not affect zoospore settlement at the interfaces of the organic solvents and water. However, zoospores settled and created mycelial networks only at HD-water interfaces. Both bacteria diminished the toxic influence of PAHs on zoospore formation and taxis, and they did not interrupt zoospore settlement. The results suggest that zoospore development could be applicable for toxicity assessment of PAHs and enhancement of their bioavailability. Microbial interactions during both swimming modes and community formation at pollutant interfaces were revealed as major factors that have potential relevance to bioremediation. PMID:25617701

  4. (E)-2,2-Dimethyl-5-(3-phenyl-allyl-idene)-1,3-dioxane-4,6-dione.

    PubMed

    Zeng, Wu-Lan

    2010-01-01

    The title compound, C(15)H(14)O(4), was prepared by the reaction of 2,2-dimethyl-1,3-dioxane-4,6-dione and (Z)-3-phenyl-acryl-aldehyde in ethanol. The dioxane ring is in a sofa conformation with the C atom bonded to the two methyl groups forming the flap. With the exception of the flap atom and the methyl group C atoms, all other non-H atoms are essentially planar, with an r.m.s. deviation of 0.067 (1) Å. The crystal structure is stabilized by weak inter-molecular C-H⋯O hydrogen bonds. PMID:21589113

  5. Particle-bound PAHs quantification using a 3-stages cascade impactor in French indoor environments.

    PubMed

    Liaud, Céline; Dintzer, Thierry; Tschamber, Valérie; Trouve, Gwénaëlle; Le Calvé, Stéphane

    2014-12-01

    Cascade Impactor is a powerful sampling method to collect airborne particles as a function of their size. The 3-stages Cascade Impactor used in this study allowed to sample simultaneously particles with aerodynamic diameter Dae>10 μm, 2.5 μmPAHs) bound to particles were quantified for 8 different indoor environments located in Strasbourg area in France. All the heavy PAHs owning between 4 and 6 aromatic rings were detected in all of the 8 sampling sites. The total PAHs concentration varied from 0.44 to 2.09 ng m(-3) for a low-energy building school and a smoking apartment, respectively. Results revealed also that high molecular weight PAHs were mainly associated to the finest particles. Our data are consistent with those measured elsewhere in European indoor environments. PMID:25194273

  6. On the driving force of PAH production

    NASA Technical Reports Server (NTRS)

    Frenklach, Michael

    1989-01-01

    The kinetic factors affecting the production of polycyclic aromatic hydrocarbons (PAH) in high-temperature pyrolysis and combustion environments are analyzed. A lumped kinetic model representing polymerization-type growth by one irreversible step and two reversible steps is considered. It is shown that at high temperatures, PAH growth is controlled by the superequilibrium of hydrogen atoms; at low temperatures and low H2 concentrations, the PAH growth rate is proportional to the rate of the H-abstraction of a hydrogen atom from aromatic molecules; while at low temperatures and high H2 concentrations, it is controlled by the thermodynamics of the H-abstraction and the kinetics of acetylene addition to aromatic radicals. The presence of oxygen mainly affects the small-molecule reactions during the induction period.

  7. A novel approach to investigating indoor/outdoor pollution links: Combined magnetic and PAH measurements

    NASA Astrophysics Data System (ADS)

    Halsall, C. J.; Maher, B. A.; Karloukovski, V. V.; Shah, P.; Watkins, S. J.

    In a preliminary study, paired indoor and outdoor air sampling was conducted at three locations around the city of Lancaster, UK to examine the influence of combustion sources on air quality by measuring particulate concentrations, particulate magnetic properties and polyaromatic hydrocarbons (PAHs). With one exception (an indoor suburban air sample), outdoor air samples had higher total suspended particulates (TSP), particle-bound PAH concentrations and magnetic remanence (IRM) values. IRM values were highest for the week-day, outdoor city centre samples and then declined in the sequence: Sunday, city centre > suburban/residential > Lancaster University campus. These data indicate traffic as the major particle-bound PAH, particulates and magnetic source, particularly as sampling was conducted during July in the absence of any space heating. The indoor air samples revealed a wide variation in pollutant concentrations, characterised by higher vapour levels of 2-3 ring PAHs, variable TSP concentrations and variable but generally low IRMs. The differences in PAH concentrations, TSP and IRMs between outdoor and indoor environments indicate limited ingress of outdoor air pollutants to the indoor environment in this study. Our combined PAH and magnetic data identify specific and distinctive indoor pollution signals for each of our sampled sites, reflecting distinct sources. One site, the suburban house, has anomalously high IRM, TSP and particle-bound PAHs. A possible source for these is a cast-iron, wood-burning stove (even though not lit). The city centre indoor site is characterised by high TSP and very low IRMs but high values of the magnetic ratio of anhysteretic remanence:saturation remanence, indicative of ultrafine (sub-micrometre) magnetic grain sizes. The source for this city centre indoor signature is unidentified but may reflect the occupant smoking and/or lighting candles. The indoor campus sample was affected by loss-on-ignition procedures carried out in a

  8. Polycyclic aromatic hydrocarbons (PAHs) and their derivatives (alkyl-PAHs, oxygenated-PAHs, nitrated-PAHs and azaarenes) in urban road dusts from Xi'an, Central China.

    PubMed

    Wei, Chong; Bandowe, Benjamin A Musa; Han, Yongming; Cao, Junji; Zhan, Changlin; Wilcke, Wolfgang

    2015-09-01

    Urban road dusts are carriers of polycyclic aromatic compounds (PACs) and are therefore considered to be a major source of contamination of other environmental compartments and a source of exposure to PACs for urban populations. We determined the occurrence, composition pattern and sources of several PACs (29 alkyl- and parent-PAHs, 15 oxygenated-PAHs (OPAHs), 4 azaarenes (AZAs), and 11 nitrated-PAHs (NPAHs)) in twenty urban road dusts and six suburban surface soils (0-5cm) from Xi'an, central China. The average concentrations of ∑29PAHs, ∑4AZAs, ∑15OPAHs, and ∑11NPAHs were 15767, 673, 4754, and 885 n gg(-1) in road dusts and 2067, 784, 854, and 118 ng g(-1) in surface soils, respectively. The concentrations of most individual PACs were higher in street dusts than suburban soils, particularly for PACs with molecular weight>192 g mol(-1). The enrichment factors of individual PACs were significantly positively correlated with log KOA and log KOW, indicating an increasing deposition and co-sorption of the PACs in urban dusts with decreasing volatility and increasing hydrophobicity. Significant correlations between the concentrations of individual and sum of PACs, carbon fractions (soot and char), and source-characteristic PACs (combustion-derived PAHs and retene, etc.), indicated that PAHs, OPAHs and AZAs were mostly directly emitted from combustion activities and had similar post-emission fates, but NPAHs were possibly more intensely photolyzed after deposition as well as being emitted from vehicle exhaust sources. The incremental lifetime cancer risk (ILCR) resulting from exposure to urban dust bound-PACs was higher than 10(-6), indicating a non-negligible cancer risk to residents of Xi'an. PMID:25543159

  9. Vascular rings.

    PubMed

    Backer, Carl L; Mongé, Michael C; Popescu, Andrada R; Eltayeb, Osama M; Rastatter, Jeffrey C; Rigsby, Cynthia K

    2016-06-01

    The term vascular ring refers to congenital vascular anomalies of the aortic arch system that compress the esophagus and trachea, causing symptoms related to those two structures. The most common vascular rings are double aortic arch and right aortic arch with left ligamentum. Pulmonary artery sling is rare and these patients need to be carefully evaluated for frequently associated tracheal stenosis. Another cause of tracheal compression occurring only in infants is the innominate artery compression syndrome. In the current era, the diagnosis of a vascular ring is best established by CT imaging that can accurately delineate the anatomy of the vascular ring and associated tracheal pathology. For patients with a right aortic arch there recently has been an increased recognition of a structure called a Kommerell diverticulum which may require resection and transfer of the left subclavian artery to the left carotid artery. A very rare vascular ring is the circumflex aorta that is now treated with the aortic uncrossing operation. Patients with vascular rings should all have an echocardiogram because of the incidence of associated congenital heart disease. We also recommend bronchoscopy to assess for additional tracheal pathology and provide an assessment of the degree of tracheomalacia and bronchomalacia. The outcomes of surgical intervention are excellent and most patients have complete resolution of symptoms over a period of time. PMID:27301603

  10. Influence of PAHs among other coastal environmental variables on total and PAH-degrading bacterial communities.

    PubMed

    Sauret, Caroline; Tedetti, Marc; Guigue, Catherine; Dumas, Chloé; Lami, Raphaël; Pujo-Pay, Mireille; Conan, Pascal; Goutx, Madeleine; Ghiglione, Jean-François

    2016-03-01

    We evaluated the relative impact of anthropogenic polycyclic aromatic hydrocarbons (PAHs) among biogeochemical variables on total, metabolically active, and PAH bacterial communities in summer and winter in surface microlayer (SML) and subsurface seawaters (SSW) across short transects along the NW Mediterranean coast from three harbors, one wastewater effluent, and one nearshore observatory reference site. At both seasons, significant correlations were found between dissolved total PAH concentrations and PAH-degrading bacteria that formed a gradient from the shore to nearshore waters. Accumulation of PAH degraders was particularly high in the SML, where PAHs accumulated. Harbors and wastewater outfalls influenced drastically and in a different way the total and active bacterial community structure, but they only impacted the communities from the nearshore zone (<2 km from the shore). By using direct multivariate statistical analysis, we confirmed the significant effect of PAH concentrations on the spatial and temporal dynamic of total and active communities in this area, but this effect was putted in perspective by the importance of other biogeochemical variables. PMID:26122564

  11. Biological Degradation of 2,4,6-Trinitrotoluene

    PubMed Central

    Esteve-Núñez, Abraham; Caballero, Antonio; Ramos, Juan L.

    2001-01-01

    Nitroaromatic compounds are xenobiotics that have found multiple applications in the synthesis of foams, pharmaceuticals, pesticides, and explosives. These compounds are toxic and recalcitrant and are degraded relatively slowly in the environment by microorganisms. 2,4,6-Trinitrotoluene (TNT) is the most widely used nitroaromatic compound. Certain strains of Pseudomonas and fungi can use TNT as a nitrogen source through the removal of nitrogen as nitrite from TNT under aerobic conditions and the further reduction of the released nitrite to ammonium, which is incorporated into carbon skeletons. Phanerochaete chrysosporium and other fungi mineralize TNT under ligninolytic conditions by converting it into reduced TNT intermediates, which are excreted to the external milieu, where they are substrates for ligninolytic enzymes. Most if not all aerobic microorganisms reduce TNT to the corresponding amino derivatives via the formation of nitroso and hydroxylamine intermediates. Condensation of the latter compounds yields highly recalcitrant azoxytetranitrotoluenes. Anaerobic microorganisms can also degrade TNT through different pathways. One pathway, found in Desulfovibrio and Clostridium, involves reduction of TNT to triaminotoluene; subsequent steps are still not known. Some Clostridium species may reduce TNT to hydroxylaminodinitrotoluenes, which are then further metabolized. Another pathway has been described in Pseudomonas sp. strain JLR11 and involves nitrite release and further reduction to ammonium, with almost 85% of the N-TNT incorporated as organic N in the cells. It was recently reported that in this strain TNT can serve as a final electron acceptor in respiratory chains and that the reduction of TNT is coupled to ATP synthesis. In this review we also discuss a number of biotechnological applications of bacteria and fungi, including slurry reactors, composting, and land farming, to remove TNT from polluted soils. These treatments have been designed to achieve

  12. Quantum mechanical and experimental analyses of TNT metabolite 2-hydroxylamino-4,6-dinitrotoluene

    NASA Astrophysics Data System (ADS)

    Junk, Thomas; Liu, Yuemin; Li, Zhong; Perkins, Richard; Liu, Yucheng

    2015-01-01

    In this study, a combined quantum mechanical and experimental analyses were performed to investigate crystal structure of the immediate degradation product of TNT, 2-hydroxylamino-4,6-dinitrotoluene (2-HADNT) and to reveal its important chemical properties. Leakage of 2-HADNT has caused serious environmental pollution and therefore raises widespread concerns. In the quantum mechanical analysis, the B3LYP/6-311+G**, B3LYP/aug-c-pVDZ, M06HF/aug-cc-pVDZ, and MP2/aug-cc-pVDZ methods were employed for geometrical optimization and single point calculations of chemical properties of the compound. Such properties include highest unoccupied molecular orbitals (HOMO) - lowest occupied molecular orbitals (LUMO) separation, dipole moment, atomization energy, and vibrational frequencies. Experimental analysis and validation showed that the energy minimized structures acquired from the quantum mechanical analysis were very similar to those obtained by X-ray crystallography. The 6-NO2 groups twist out of plane with respect to the benzene ring in both the crystallographic and energy minimized structures. The 4-NO2 group exhibits co-planarity with the phenyl ring in both the crystallographic and energy minimized structures as well. Unlike TNT, however, the energy barrier to orthogonal conformation is only 3.8 kcal/mol. In addition, considerable discrepancies between results obtained from the MP2 and B3LYP methods were observed, which suggest that it has to be very careful when applying B3LYP method to study such class of compounds. Through this study, a more accurate description of the chemical properties of dispersion-dominated aromatic systems was acquired. The chemical properties found from this study can help researchers to better understand the compound of 2-HADNT and to develop effective management plans for such compound so as to minimize its impact on the environment.

  13. Time trends in the levels and patterns of polycyclic aromatic hydrocarbons (PAHs) in pine bark, litter, and soil after a forest fire.

    PubMed

    Choi, Sung-Deuk

    2014-02-01

    Forest fires are known as an important natural source of polycyclic aromatic hydrocarbons (PAHs), but time trends of PAH levels and patterns in various environmental compartments after forest fires have not been thoroughly studied yet. In this study, 16 US-EPA priority PAHs were analyzed for pine bark, litter, and soil samples collected one, three, five, and seven months after a forest fire in Pohang, South Korea. At the first sampling event, the highest levels of ∑16 PAHs were measured for the three types of samples (pine bark: 5,920 ng/g, litter: 1,540 ng/g, and soil: 133 ng/g). Thereafter, there were apparent decreasing trends in PAH levels; the control samples showed the lowest levels (pine bark: 124 ng/g, litter: 75 ng/g, and soil: 26 ng/g). The levels of PAHs in the litter and soil samples normalized by organic carbon (OC) fractions also showed decreasing trends, indicating a direct influence of the forest fire. Among the 16 target PAHs, naphthalene was a dominant compound for all types of samples. Light PAHs with 2-4 rings significantly contributed to the total concentration, and their contribution decreased in the course of time. Runoff by heavy precipitation, evaporation, and degradation of PAHs in the summer were probably the main reasons for the observed time trends. The results of principal component analysis (PCA) and diagnostic ratio also supported that the forest fire was indeed an important source of PAHs in the study area. PMID:23972323

  14. ASSESSING RISKS FROM PHOTOACTIVATED TOXICITY OF PAHS TO AQUATIC ORGANISMS

    EPA Science Inventory

    Polycyclic aromatic hydrocarbons (PAHs) are one of the most ubiquitous classes of environmental contaminants. Although most PAHs are toxic only at concentrations large enough to cause narcosis, the toxicity of some can be greatly enhanced through mechanisms that involve molecul...

  15. Vertical profile, source apportionment, and toxicity of PAHs in sediment cores of a wharf near the coal-based steel refining industrial zone in Kaohsiung, Taiwan.

    PubMed

    Chen, Chih-Feng; Chen, Chiu-Wen; Ju, Yun-Ru; Dong, Cheng-Di

    2016-03-01

    Three sediment cores were collected from a wharf near a coal-based steel refining industrial zone in Kaohsiung, Taiwan. Analyses for 16 polycyclic aromatic hydrocarbons (PAHs) of the US Environmental Protection Agency priority list in the core sediment samples were conducted using gas chromatography-mass spectrometry. The vertical profiles of PAHs in the core sediments were assessed, possible sources and apportionment were identified, and the toxicity risk of the core sediments was determined. The results from the sediment analyses showed that total concentrations of the 16 PAHs varied from 11774 ± 4244 to 16755 ± 4593 ng/g dry weight (dw). Generally, the vertical profiles of the PAHs in the sediment cores exhibited a decreasing trend from the top to the lower levels of the S1 core and an increasing trend of PAHs from the top to the lower levels of the S2 and S3 cores. Among the core sediment samples, the five- and six-ring PAHs were predominantly in the S1 core, ranging from 42 to 54 %, whereas the composition of the PAHs in the S2 and S3 cores were distributed equally across three groups: two- and three-ring, four-ring, and five- and six-ring PAHs. The results indicated that PAH contamination at the site of the S1 core had a different source. The molecular indices and principal component analyses with multivariate linear regression were used to determine the source contributions, with the results showing that the contributions of coal, oil-related, and vehicle sources were 38.6, 35.9, and 25.5 %, respectively. A PAH toxicity assessment using the mean effect range-median quotient (m-ERM-q, 0.59-0.79), benzo[a]pyrene toxicity equivalent (TEQ(carc), 1466-1954 ng TEQ/g dw), and dioxin toxicity equivalent (TEQ(fish), 3036-4174 pg TEQ/g dw) identified the wharf as the most affected area. The results can be used for regular monitoring, and future pollution prevention and management should target the coal-based industries in this region for pollution reduction

  16. A Graphene-Based Nanosensor for In Situ Monitoring of Polycyclic Aromatic Hydrocarbons (PAHs).

    PubMed

    Church, Jared; Wang, Xiaochen; Calderon, Jean; Lee, Woo Hyoung; Cho, Hyoung J; Zhai, Lei

    2016-02-01

    A graphene-based nanosensor was developed for in situ monitoring of polycyclic aromatic hydrocarbons (PAHs) in aqueous solutions. The sensor was fabricated using photolithography and etching of Au/Ti film on a silicon wafer followed by the transfer of a single graphene layer which was prepared separately by chemical vapor deposition (CVD). The performance of the graphene nanosensor was characterized using electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). The graphene-based sensor demonstrated a fast (<10 sec) and linear response to toluene (0 to 17 ppm) at +400 mV versus Ag/AgCl when measured amperometrically. The novelty can be found in utilizing high affinity of graphene to PAHs and intermolecular electron delocalization at the interface of graphene and a benzene ring for toluene detection in water. The developed sensor is applicable to many contaminated water bodies or engineered systems due to its reduced sensing cost, portability, and ease of use. PMID:27433633

  17. Element and PAH constituents in the residues and liquid oil from biosludge pyrolysis in an electrical thermal furnace.

    PubMed

    Chiang, Hung-Lung; Lin, Kuo-Hsiung; Lai, Nina; Shieh, Zhu-Xin

    2014-05-15

    Biosludge can be pyrolyzed to produce liquid oil as an alternative fuel. The content of five major elements, 22 trace elements and 16 PAHs was investigated in oven-dried raw material, pyrolysis residues and pyrolysis liquid products. Results indicated 39% carbon, 4.5% hydrogen, 4.2% nitrogen and 1.8% sulfur were in oven dried biosludge. Biosludge pyrolysis, carried out at temperatures from 400 to 800°C, corresponded to 34-14% weight in pyrolytic residues, 32-50% weight in liquid products and 31-40% weight in the gas phase. The carbon, hydrogen and nitrogen decreased and the sulfur content increased with an increase in the pyrolysis temperature at 400-800°C. NaP (2 rings) and AcPy (3 rings) were the major PAHs, contributing 86% of PAHs in oven-dried biosludge. After pyrolysis, the PAH content increased with the increase of pyrolysis temperature, which also results in a change in the PAH species profile. In pyrolysis liquid oil, NaP, AcPy, Flu and PA were the major species, and the content of the 16 PAHs ranged from 1.6 to 19 μg/ml at pyrolysis temperatures ranging from 400 to 800°C. Ca, Mg, Al, Fe and Zn were the dominant trace elements in the raw material and the pyrolysis residues. In addition, low toxic metal (Cd, V, Co, and Pb) content was found in the liquid oil, and its heat value was 7,800-9,500 kcal/kg, which means it can be considered as an alternative fuel. PMID:24631616

  18. Models of 2,4,6-trinitrotoluene (TNT) initial conversion by yeasts.

    PubMed

    Zaripov, S A; Naumov, A V; Abdrakhmanova, J F; Garusov, A V; Naumova, R P

    2002-12-17

    The original models of the initial steps of 2,4,6-trinitrotoluene (TNT) conversion by yeasts are presented. Saccharomyces sp. ZS-A1 reduced nitro groups of TNT producing isomeric monohydroxylaminodinitrotoluenes (HADNT) as the key initial metabolites (molar ratio HADNT/TNT was up to 0.81), whereas aminodinitrotoluenes (ADNT) and the hydride-Meisenheimer complex of TNT (H-TNT) were the minor products. Conversely, Candida sp. AN-L13 transformed TNT almost quantitatively into H-TNT, thus realizing the alternative attack, consisting of the TNT aromatic ring reduction. The third type of conversion, revealed in Candida sp. AN-L14, is the combination of both above mechanisms and produces an equimolar mix of HADNT and H-TNT. In the toxicity tests with Paramecium caudatum, the supernatant of Saccharomyces sp. ZS-A1, which converts TNT into HADNT, was most toxic while the supernatant of Candida sp. AN-L13 (TNT --> H-TNT) was least toxic. The microorganisms converting TNT quantitatively to the reactive metabolites can be useful for their immobilization through the detoxifying interaction with the soil components such as humic compounds. PMID:12480106

  19. Irreversible binding of biologically reduced 2,4,6-trinitrotoluene to soil

    SciTech Connect

    Achtnich, C.; Sieglen, U.; Knackmuss, H.J.; Lenke, H.

    1999-11-01

    To analyze the fate of 2,4,6-trinitrotoluene (TNT) and its reduction products, a TNT-contaminated soil was spiked with [ring-UL-{sup 14}C]TNT and treated in a laboratory slurry reactor. During an anaerobic/aerobic treatment, the total radioactivity measured in the supernatant and methanolic soil extracts decreased to 2%. The decrease corresponded to an increase of strongly bound radioactivity to the soil. Throughout the whole treatment process, mineralization of TNT was not observed. During the reductive process, unidentified polar substances increased to a maximum amount of 23.2% of the total radioactivity on the day after the start of the experiment. After the end of the anaerobic phase, still 9.7% of the radioactivity was found in this fraction. Only during the aerobic phase did the polar substances disappear completely. The irreversible character of the binding of the reduced metabolites of TNT to the soil was indicated by the failure of desorption even under rigorous and long-term extraction conditions. A significant release of radioactivity could be measured only by using high concentrations of HCl or EDTA. However, in none of the extracts were TNT or any reduced metabolites detected by HPLC and {sup 14}C-radiocounting. Size-exclusion chromatography of humic acids extracted from the treated soil indicated that the metabolites of TNT were evenly bound to the complete range of molecular size of the humic acids.

  20. Degradation of 2-sec-butyl-4,6-dinitrophenol (dinoseb) by Clostridium bifermentans KMR-1.

    PubMed Central

    Hammill, T B; Crawford, R L

    1996-01-01

    A strain of Clostridium bifermentans, KMR-1, degraded 2-sec-butyl-4,6-dinitrophenol (dinoseb) to a level below the limit of detection by high-performance liquid chromatography (0.5 mg/liter) within 96 h, with no accumulation of aromatic intermediates. KMR-1 could not utilize dinoseb as a sole carbon or energy source, and degradation occurred via cometabolism in the presence of a fermentable carbon source. KMR-1 mineralized some dinoseb in anaerobic cultures, evolving 7.2% of the radioactive label in U-ring 14C-labeled dinoseb as 14CO2. The remaining anaerobic degradation products were incubated with aerobic soil bacteria, and 35.4% of this residual radioactive label was evolved as 14CO2. During this mineralization experiment, 38.9% of the initial label was evolved as 14CO2 after both anaerobic and aerobic phases. This is the first demonstration of dinoseb degradation by a pure microbial culture. PMID:8633886

  1. Probabilistic ecological risk assessment of selected PAH`s in sediments near a petroleum refinery

    SciTech Connect

    Arnold, W.R.; Biddinger, G.R.

    1995-12-31

    Sediment samples were collected and analyzed for a number of polynuclear aromatic hydrocarbons (PAHs) along a gradient from a petroleum refinery`s wastewater diffuser. These data were used to calculate the potential risk to aquatic organisms using probabilistic modeling and Monte Carlo sampling procedures. Sediment chemistry data were used in conjunction with estimates of Biota-Sediment Accumulation Factors and Non-Polar Narcosis Theory to predict potential risk to bivalves. Bivalves were the receptors of choice because of their lack of a well-developed enzymatic system for metabolizing PAHs. Thus, they represent a species of higher inherent risk of adverse impact. PAHs considered in this paper span a broad range of octanol-water partition coefficients. Results indicate negligible risk of narcotic effects from PAHs existing near the refinery wastewater discharge.

  2. Sorption and chemical transformation of PAH`s on coal fly ash

    SciTech Connect

    Mamantov, G.; Wehry, E.L.

    1995-05-09

    The major objective of this work was to characterize the interactions of coal fly ash with polycyclic aromatic hydrocarbons (PAHS) and their derivatives, and to attempt to understand the influence of the surface properties of coal ash (and other atmospheric particles) on the chemical transformations of polycyclic aromatic compounds. Our studies have concentrated on the photochemical behavior of PAHs sorbed form the vapor phase on coal fly ashes, and compositional subfractions obtained therefrom. The PAHs are deposited onto the fly ash substrates from the vapor phase, using apparatus and techniques developed in this laboratory in order to simulate, as closely as possible under laboratory conditions, the processes by which PAHs deposit onto fly ash particles in the atmosphere. In this report phototransformation of pyrene sorbed on fly ash fractions, and phototransformations of 1-nitropyrene sorbed on fly ash fractions are discussed.

  3. STUDIES ON THE MICROBIAL ECOLOGY OF PAH DEGRADATION

    EPA Science Inventory

    Soils with known history of exposure to polycyclic aromatic hydrocarbons (PAHS) were collected from Norway, Germany and the United States and screened for the presence of PAH-degrading bacteria. urified PAH-degrading isolates were characterized by fatty acid profile analysis (GC-...

  4. Storage Rings

    SciTech Connect

    Fischer, W.

    2011-01-01

    Storage rings are circular machines that store particle beams at a constant energy. Beams are stored in rings without acceleration for a number of reasons (Tab. 1). Storage rings are used in high-energy, nuclear, atomic, and molecular physics, as well as for experiments in chemistry, material and life sciences. Parameters for storage rings such as particle species, energy, beam intensity, beam size, and store time vary widely depending on the application. The beam must be injected into a storage ring but may not be extracted (Fig. 1). Accelerator rings such as synchrotrons are used as storage rings before and after acceleration. Particles stored in rings include electrons and positrons; muons; protons and anti-protons; neutrons; light and heavy, positive and negative, atomic ions of various charge states; molecular and cluster ions, and neutral polar molecules. Spin polarized beams of electrons, positrons, and protons were stored. The kinetic energy of the stored particles ranges from 10{sup -6} eV to 3.5 x 10{sup 12} eV (LHC, 7 x 10{sup 12} eV planned), the number of stored particles from one (ESR) to 1015 (ISR). To store beam in rings requires bending (dipoles) and transverse focusing (quadrupoles). Higher order multipoles are used to correct chromatic aberrations, to suppress instabilities, and to compensate for nonlinear field errors of dipoles and quadrupoles. Magnetic multipole functions can be combined in magnets. Beams are stored bunched with radio frequency systems, and unbunched. The magnetic lattice and radio frequency system are designed to ensure the stability of transverse and longitudinal motion. New technologies allow for better storage rings. With strong focusing the beam pipe dimensions became much smaller than previously possible. For a given circumference superconducting magnets make higher energies possible, and superconducting radio frequency systems allow for efficient replenishment of synchrotron radiation losses of large current electron or

  5. Impact of clay mineral, wood sawdust or root organic matter on the bacterial and fungal community structures in two aged PAH-contaminated soils.

    PubMed

    Cébron, Aurélie; Beguiristain, Thierry; Bongoua-Devisme, Jeanne; Denonfoux, Jérémie; Faure, Pierre; Lorgeoux, Catherine; Ouvrard, Stéphanie; Parisot, Nicolas; Peyret, Pierre; Leyval, Corinne

    2015-09-01

    The high organic pollutant concentration of aged polycyclic aromatic hydrocarbon (PAH)-contaminated wasteland soils is highly recalcitrant to biodegradation due to its very low bioavailability. In such soils, the microbial community is well adapted to the pollution, but the microbial activity is limited by nutrient availability. Management strategies could be applied to modify the soil microbial functioning as well as the PAH contamination through various amendment types. The impact of amendment with clay minerals (montmorillonite), wood sawdust and organic matter plant roots on microbial community structure was investigated on two aged PAH-contaminated soils both in laboratory and 1-year on-site pot experiments. Total PAH content (sum of 16 PAHs of the US-EPA list) and polar polycyclic aromatic compounds (pPAC) were monitored as well as the available PAH fraction using the Tenax method. The bacterial and fungal community structures were monitored using fingerprinting thermal gradient gel electrophoresis (TTGE) method. The abundance of bacteria (16S rRNA genes), fungi (18S rRNA genes) and PAH degraders (PAH-ring hydroxylating dioxygenase and catechol dioxygenase genes) was followed through qPCR assays. Although the treatments did not modify the total and available PAH content, the microbial community density, structure and the PAH degradation potential changed when fresh organic matter was provided as sawdust and under rhizosphere influence, while the clay mineral only increased the percentage of catechol-1,2-dioxygenase genes. The abundance of bacteria and fungi and the percentage of fungi relative to bacteria were enhanced in soil samples supplemented with wood sawdust and in the plant rhizospheric soils. Two distinct fungal populations developed in the two soils supplemented with sawdust, i.e. fungi related to Chaetomium and Neurospora genera and Brachyconidiellopsis and Pseudallescheria genera, in H and NM soils respectively. Wood sawdust amendment favoured the

  6. Exploratory study on the pyrolysis and PAH emissions of polylactic acid

    NASA Astrophysics Data System (ADS)

    Chien, Yi-Chi; Liang, Chenju; Yang, Shu-hua

    2011-01-01

    The emission factors for 16 U.S. EPA priority polycyclic aromatic hydrocarbons (PAHs) from the polylactic acid (PLA) pyrolysis and the decomposition mechanism were investigated in this study. The fragments and gas compositions using on-line thermogravimetry-mass spectrometry (TG-MS) were determined. A temperature series of 7 fragments was analyzed in helium, and was found to include: m/z = 16, which may represent methane; 28, which may be carbon monoxide; 44, which may be acetaldehyde; 56, which may be methylketene, 144, which may be oligomers of lactide. In addition, there are little amount of 100, and 200 which are oligomers of lactides observed in the pyrolysis of PLA. The pyrolysis of PLA is a non-radical, backbiting ester interchange reaction involving the OH chain ends. Depending on the size of the cyclic transition state, the product can be a lactide molecule, an oligomeric ring with more than two repeat units, methylketene, or acetaldehyde. Carbon monoxide and methane are contributions from the decomposition of acetaldehyde. Experimentally, not detected (n.d.)-40.47 μg of 16 PAH emissions were determined from per gram of PLA pyrolysis. The PAH profiles showed a predominance of naphthalene (58.9%), phenanthrene (12.5%), and fluoranthene (5.9%). The total PAH emissions for PLA pyrolysis is significantly lower than the values associated with PLA combustion. From the viewpoint of air pollution control, this result suggests that pyrolysis seems a better alternative than combustion for the disposal of waste PLA. Also, since pyrolysis is the first step for an incineration process, these results can provide important information on the control of PAHs formation for a commercialized incinerator.

  7. [PAHs concentrations in aquatic products and food safety evaluation in the coupled mangrove planting-aquaculture ecological system].

    PubMed

    Chen, Guan-Qiu; Li, Yao-Chu; Huang, Jin-Mu; Nan, Yan; Lin, Mao-Hong

    2012-06-01

    In order to know about the PAHs concentration in aquatic products from mangrove planting-aquaculture ecological system and to make sure of food quality and food safety, HPLC was used to determine concentrations of 13 polycyclic aromatic hydrocarbons (PAHs) in the Tilapia mossambica, Mugil cephalu and Concha ostreae from coupled mangrove planting-aquaculture ponds, food safety in aquatic products was also evaluated. The 13 PAHs were Fluorene (Flu), Phenanthrene (Phe), Anthracene (Ant), Fluoranthene (Fla), Pyrene (Pyr), Benz[a] anthraces (BaA), Chrysene (Chr), Benzo[b] fluoranthene (BbF), Benzo[k] fluoranthene (BkF), Benzo[a] Pyrene (BaP), Dibenzo [a, h] anthercene (DahA), Benzo [g, h, i] perylene (BghiP) and Indeno [1,2,3-c, d] pyrene (InP). Concentrations of PAHs were the highest in Concha ostreae which were in the range of 89.79-98.49 microg x kg(-1) dry weight, while those were in the range of 25.97-34.64 microg x kg(-1) in Mugil cephalu and 12.31-14.41 microg x kg(-1) in Tilapia mossambica. The content of fat affected the levels of PAHs content in different aquatic products. The individual composition of PAHs was characterized by 3 rings in samples with the range of 41.58% - 83.35%. Comparing with other areas, PAHs pollution of aquatic products in the studied area was in the mild level. Values of the total BaP(eq) concentration ranged from 0.0689 microg x kg(-1) to 1.0373 microg x kg(-1), which were lower than the maximum level set by European Union. PMID:22946164

  8. Modeling the adsorption of PAH mixture in silica nanopores by molecular dynamic simulation combined with machine learning.

    PubMed

    Sui, Hong; Li, Lin; Zhu, Xinzhe; Chen, Daoyi; Wu, Guozhong

    2016-02-01

    The persistence of polycyclic aromatic hydrocarbons (PAHs) in contaminated soils is largely controlled by their molecular fate in soil pores. The adsorption and diffusion of 16 PAHs mixture in silica nanopore with diameter of 2.0, 2.5, 3.0 and 3.5 nm, respectively, were characterized by adsorption energy, mean square displacement, free surface area and free volume fraction using molecular dynamic (MD) simulation. Results suggested that PAHs adsorption in silica nanopores was associated with diffusion process while competitive sorption was not the dominant mechanism in context of this study. The partial least squares (PLS) regression and machine learning (ML) methods (i.e. support vector regression, M5 decision tree and multilayer perceptrons) were used to correlate the adsorption energy with the pore diameter and PAH properties (number of carbon atoms, aromatic ring number, boiling point, molecular weight, octanol-water partition coefficient, octanol-organic carbon partition coefficient, solvent accessible area, solvent accessible volume and polarization). Results indicated that the PAH adsorption could not be predicted by linear regression as the R(2)Y and Q(2)Y coefficients of PLS analysis was 0.375 and 0.199, respectively. The nonlinearity was well recognized by ML with correlation coefficient up to 0.9. Overall, the combination of MD simulation and ML approaches can assist in interpreting the sequestration of organic contaminants in the soil nanopores. PMID:26547031

  9. Ring Galaxies

    NASA Astrophysics Data System (ADS)

    Dennefeld, M.; Materne, J.

    1980-09-01

    Among the 338 exotic, intriguing and/or fascinating objects contained in Arp's catalogue of peculiar galaxies, two, Arp 146 and 147, are calling special attention as a presumably separate class of objects displaying closed rings with almost empty interior. It is difficult to find out when, historically speaking, attention was called first to this type of object as a peculiar class, but certainly ga1axies with rings were widely found and recognized in the early sixties, ul}der others by Vorontsov-Velyaminov (1960), Sandage (1961) in the Hubble Atlas or de Vaucouleurs (1964) in the first reference catalogue of ga1axies. The most recent estimates by Arp and Madore (1977) from a search on about 200 Schmidt plates covering 7,000 square degrees give 3.6 per cent of ring galaxies among 2,784 peculiar galaxies found. However, despite the mythological perfection associated with a circle, some ordering is necessary before trying to understand the nature of such objects. This is particularly true because a large fraction of those galaxies with rings are probably normal spiral galaxies of type RS or S(r) as defined by de Vaucouleurs, where the spiral arms are simply "closing the circle". A good example of such "ordinary" galaxy is NGC 3081 in the Hubble Atlas .

  10. Are urinary PAHs biomarkers of controlled exposure to diesel exhaust?

    PubMed Central

    Lu, Sixin S.; Sobus, Jon R.; Sallsten, Gerd; Albin, Maria; Pleil, Joachim D.; Gudmundsson, Anders; Madden, Michael C.; Strandberg, Bo; Wierzbicka, Aneta; Rappaport, Stephen M.

    2016-01-01

    Urinary polycyclic aromatic hydrocarbons (PAHs) were evaluated as possible biomarkers of exposure to diesel exhaust (DE) in two controlled-chamber studies. We report levels of 14 PAHs from 28 subjects in urine that were collected before, immediately after and the morning after exposure. Using linear mixed-effects models, we tested for effects of DE exposure and several covariates (time, age, gender and urinary creatinine) on urinary PAH levels. DE exposures did not significantly alter urinary PAH levels. We conclude that urinary PAHs are not promising biomarkers of short-term exposures to DE in the range of 106–276 μg/m3. PMID:24754404

  11. 2,2-Dimethyl-5-(2-nitro­benzyl­idene)-1,3-dioxane-4,6-dione

    PubMed Central

    García-Álvarez, Fernando; Romero, Nancy; Lobato-García, Carlos E.; Terán, Joel L.; Mendoza, Angel

    2013-01-01

    The asymmetric unit of the title compound, C13H11NO6, contains two mol­ecules in both of which the six-membered 1,3-dioxane-4,6-dione ring shows a screw-boat conformation. The dihedral angles between the best planes through the six-membered rings are 47.8 (2) and 49.8 (2)°. In the crystal, C—H⋯O inter­actions link the mol­ecules, building a supramolecular sheet parallel to the c axis. PMID:23476434

  12. Conserved themes in target recognition by the PAH1 and PAH2 domains of the Sin3 transcriptional corepressor.

    PubMed

    Sahu, Sarata C; Swanson, Kurt A; Kang, Richard S; Huang, Kai; Brubaker, Kurt; Ratcliff, Kathleen; Radhakrishnan, Ishwar

    2008-02-01

    The recruitment of chromatin-modifying coregulator complexes by transcription factors to specific sites of the genome constitutes an important step in many eukaryotic transcriptional regulatory pathways. The histone deacetylase-associated Sin3 corepressor complex is recruited by a large and diverse array of transcription factors through direct interactions with the N-terminal PAH domains of Sin3. Here, we describe the solution structures of the mSin3A PAH1 domain in the apo form and when bound to SAP25, a component of the corepressor complex. Unlike the apo-mSin3A PAH2 domain, the apo-PAH1 domain is conformationally pure and is largely, but not completely, folded. Portions of the interacting segments of both mSin3A PAH1 and SAP25 undergo folding upon complex formation. SAP25 binds through an amphipathic helix to a predominantly hydrophobic cleft on the surface of PAH1. Remarkably, the orientation of the helix is reversed compared to that adopted by NRSF, a transcription factor unrelated to SAP25, upon binding to the mSin3B PAH1 domain. The reversal in helical orientations is correlated with a reversal in the underlying PAH1-interaction motifs, echoing a theme previously described for the mSin3A PAH2 domain. The definition of these so-called type I and type II PAH1-interaction motifs has allowed us to predict the precise location of these motifs within previously experimentally characterized PAH1 binders. Finally, we explore the specificity determinants of protein-protein interactions involving the PAH1 and PAH2 domains. These studies reveal that even conservative replacements of PAH2 residues with equivalent PAH1 residues are sufficient to alter the affinity and specificity of these protein-protein interactions dramatically. PMID:18089292

  13. Measurement of polynuclear aromatic hydrocarbons (PAHs) in epiphytic lichens and from PM 2.5 filters for receptor modeling in the Alberta Oil Sands Region (Invited)

    NASA Astrophysics Data System (ADS)

    Studabaker, W. B.; Jayanty, J.; Raymer, J. H.; Krupa, S.

    2013-12-01

    contribution of low ring number PAHs to total PAHs increased with increasing distance. Total PAHs correlated strongly (R2 > 0.80, p < 0.05) with crustal elements, suggesting similar transport mechanisms. Analytical data for PAHs on PM 2.5 filters, including relationships between concentrations, PAH profiles, and distance from the mines, will be presented. The lichen data are consistent with PAH transport close to the mines being more influenced by particulate matter transport mechanisms, whereas PAHs in samples collected from remote areas reflect more of the vapor phase transport mechanisms.

  14. Rapid persulfate oxidation predicts PAH bioavailability in soils and sediments

    SciTech Connect

    Cuypers, C.; Grotenhuis, T.; Joziasse, J.; Rulkens, W.

    2000-05-15

    Persulfate oxidation was validated as a method to predict polycyclic aromatic hydrocarbon (PAH) bioavailability in soils and sediments. It was demonstrated for 14 field contaminated soils and sediments that residual PAH concentrations after a short (3 h) persulfate oxidation correspond well to residual PAH concentrations after 21 days of biodegradation. Persulfate oxidation of samples that had first been subjected to biodegradation yielded only limited additional PAH oxidation. This implies that oxidation and biodegradation removed approximately the same PAH fraction. Persulfate oxidation thus provides a good and rapid method for the prediction of PAH bioavailability. Thermogravimetric analysis of oxidized and untreated samples showed that persulfate oxidation primarily affected expanded organic matter. The results indicate that this expanded organic matter contained mainly readily bioavailable PAHs.

  15. Biomonitoring of air quality in the Cologne Conurbation using pine needles as a passive sampler—Part II: polycyclic aromatic hydrocarbons (PAH)

    NASA Astrophysics Data System (ADS)

    Lehndorff, E.; Schwark, L.

    Emissions from fossil fuel combustion pose a serious thread to public health and impose the need for an improved monitoring of polycyclic aromatic hydrocarbons (PAH), a major class of persistent organic pollutants. For this purpose, utilization of evergreen conifers offers significant biomonitoring potential. In part I of this series we inspected the load of combustion derived magnetic particles in pine needles from 43 locations of the Cologne Conurbation, Germany; we here report the corresponding PAH concentrations and distribution patterns. Concentrations (dry weight) of summed 3-6-ring PAH range between 51 and 410 ng g -1 with a median of 123.8 ng g -1; thus being in agreement with other urban studies. Phenanthrene was the dominating PAH with median concentrations of 47 ng g -1 followed by fluoranthene and pyrene at 22 and 13 ng g -1, respectively. The major proportion of PAH was attributed to traffic sources, with minor contribution from power plant, domestic heating, industrial, and vegetation burn emissions. Significant differences between major and minor roads were not observed indicating a thorough mixing of PAH-loaded air masses in the Cologne Conurbation. Needles in inner city parks gave much higher PAH concentrations than those in suburban green areas. Although distribution patterns of PAH were variable a PAH source reconciliation based on isomer compositions is difficult, due to thorough mixing of air masses and associated loss of source specificity. Ambient air monitoring in urban areas based on persistent organic pollutant load of vegetation is a feasible and cost effective way of controlling environmental quality.

  16. PAHs, NITRO-PAHs, HOPANES, AND STERANES IN LAKE TROUT FROM LAKE MICHIGAN

    PubMed Central

    Huang, Lei; Chernyak, Sergei M.; Batterman, Stuart A.

    2015-01-01

    The present study examines concentrations and risks of polycyclic aromatic hydrocarbons (PAHs), nitro-PAHs (NPAHs), steranes, and hopanes in lake trout collected in Lake Michigan. A total of 74 fish were collected in 2 seasons at 3 offshore sites. The total PAH concentration (Σ9PAH) in whole fish ranged from 223 pg/g to 1704 pg/g wet weight, and PAH concentrations and profiles were similar across season, site, and sex. The total NPAH (Σ9NPAH) concentrations ranged from 0.2 pg/g to 31 pg/g wet weight, and carcinogenic compounds, including 1-nitropyrene and 6-nitrochrysene, were detected. In the fall, NPAH concentrations were low at the Illinois site (0.2–0.5 pg/g wet wt), and site profiles differed considerably; in the spring, concentrations and profiles were similar across sites, possibly reflecting changes in fish behavior. In the fall, the total sterane (Σ5Sterane) and total hopane (Σ2Hopane) levels reached 808 pg/g and 141 pg/g wet weight, respectively, but concentrations in the spring were 10 times lower. Concentrations in eggs (fall only) were on the same order of magnitude as those in whole fish. These results demonstrate the presence of target semivolatile organic compounds in a top predator fish, and are consistent with PAH biodilution observed previously. Using the available toxicity information for PAHs and NPAHs, the expected cancer risk from consumption of lake trout sampled are low. However, NPAHs contributed a significant portion of the toxic equivalencies in some samples. The present study provides the first measurements of NPAHs in freshwater fish, and results suggest that additional assessment is warranted. PMID:24764175

  17. PAH Accessibility in Particulate Matter from Road-Impacted Environments.

    PubMed

    Allan, Ian J; O'Connell, Steven G; Meland, Sondre; Bæk, Kine; Grung, Merete; Anderson, Kim A; Ranneklev, Sissel B

    2016-08-01

    Snowmelt, surface runoff, or stormwater releases in urban environments can result in significant discharges of particulate matter-bound polycyclic aromatic hydrocarbons (PAHs) into aquatic environments. Recently, more-specific activities such as road-tunnel washing have been identified as contributing to contaminant load to surface waters. However, knowledge of PAH accessibility in particulate matter (PM) of urban origin that may ultimately be released into urban surface waters is limited. In the present study, we evaluated the accessibility of PAHs associated with seven distinct (suspended) particulate matter samples collected from different urban sources. Laboratory-based infinite sink extractions with silicone rubber (SR) as the extractor phase demonstrated a similar pattern of PAH accessibility for most PM samples. Substantially higher accessible fractions were observed for the less-hydrophobic PAHs (between 40 and 80% of total concentrations) compared with those measured for the most-hydrophobic PAHs (<5% of total concentrations). When we focused on PAHs bound to PM from tunnel-wash waters, first-order desorption rates for PAHs with log Kow > 5.5 were found in line with those commonly found for slowly or very slowly desorbing sediment-associated contaminants. PAHs with log Kow < 5.5 were found at higher desorbing rates. The addition of detergents did not influence the extractability of lighter PAHs but increased desorption rates for the heavier PAHs, potentially contributing to increases in the toxicity of tunnel-wash waters when surfactants are used. The implications of total and accessible PAH concentrations measured in our urban PM samples are discussed in a context of management of PAH and PM emission to the surrounding aquatic environment. Although we only fully assessed PAHs in this work, further study should consider other contaminants such as OPAHs, which were also detected in all PM samples. PMID:27312518

  18. 2,2-Dimethyl-5-(2,3,4-trimeth-oxy-benzyl-idene)-1,3-dioxane-4,6-dione.

    PubMed

    Zeng, Wu-Lan

    2011-08-01

    The title compound, C(16)H(18)O(7), was prepared by the reaction of 2,2-dimethyl-1,3-dioxane-4,6-dione and 2,3,4-trimeth-oxy-benzaldehyde. The 1,3-dioxane ring is in a slightly distorted boat conformation. The crystal structure is stabilized by weak inter-molecular C-H⋯O hydrogen bonds. PMID:22090981

  19. 5,5'-[(2,4-Dichloro-phen-yl)methyl-ene]bis-(2,2-dimethyl-1,3-dioxane-4,6-dione).

    PubMed

    Zeng, Wu-Lan

    2011-08-01

    The title compound, C(19)H(18)Cl(2)O(8), was prepared by the reaction of 2,2-dimethyl-1,3-dioxane-4,6-dione and 2,4-dichloro-benzaldehyde in ethanol. The two 1,3-dioxane rings exhibit boat conformations. In the crystal, mol-ecules are linked by weak inter-molecular C-H⋯O and C-H⋯Cl hydrogen bonds, forming chains parallel to the a axis. PMID:22090945

  20. Photodegradation of PAHs in passive water samplers.

    PubMed

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

    2016-04-15

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

  1. 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. PMID:25257517

  2. [PAH Cations as Viable Carriers of DIBs

    NASA Technical Reports Server (NTRS)

    Snow, Ted

    1998-01-01

    This report is intended to fill in the blanks in NASA's file system for our lab astro study of molecular ions of astrophysical interest. In order to give NASA what it needs for its files, I attach below the text of the section from our recent proposal to continue this work, in which we describe progress to date, including a large number of publications. Our initial studies were focused on PAH cations, which appear to be viable candidates as the carriers of the DIBs, an idea that has been supported by laboratory spectroscopy of PAH cations in inert matrices. Beginning with the simplest aromatic (benzene; C6H6) and moving progressively to larger species (naphthalene, C10OH8; pyrene, C16H10; and most recently chrysene, C18H12), we have been able to derive rate coefficients for reactions with neutral spices that are abundant in the diffuse interstellar medium.

  3. Levels and distribution of organochlorine pesticides (OCPs) and polycyclic aromatic hydrocarbons (PAHs) in topsoils from SE Romania.

    PubMed

    Ene, Antoaneta; Bogdevich, Oleg; Sion, Alina

    2012-11-15

    The aim of this work was to determine the concentrations of organochlorine pesticides (OCPs) and polycyclic aromatic hydrocarbons (PAHs) in topsoils (n=17) at two sampling depths in Southeastern Romania, including industrial (Galati iron and steel plant) and agricultural sites in Galati and Braila counties, as well as nature reserves such as Lower Prut Meadow (Galati County) and Bugeac Lake (Constanta County), and to compare them with national guidelines and values reported for other regions. The total detectable OCP concentrations vary in the ranges 58-1662ngg(-1) dry weight (dw) for 0-5cm depth and 6-12,644ngg(-1) dw for 5-20cm depth. Of these, the concentrations of HCHs, DDTs, and heptachlor varied in the ranges 6-6818ngg(-1), 27-5826ngg(-1), and 108-873ngg(-1) dw, respectively, the highest values being registered near a cultivated area, located in the proximity of Siret River and Galati town, probably due to extensive use of pesticides in the past. Chlordane was detected only at one industrial site in Galati (53ngg(-1) dw), while the levels of aldrin, dieldrin, endrin and mirex were below the detection limits in all the locations and for both depths. The total PAH concentrations for 5-20cm depth range from 9ngg(-1) (Lower Prut Meadow) to 25,352ngg(-1) dw (cattle farm), being lower than those reported for the upper 5cm layer. The PAH distribution pattern in this study is in agreement with that previously obtained for surface soils from Lower Prut Meadow (prevalence of 3-ring PAHs), industrial area and farmland (prevalence of 4- and 5-ring PAHs), their sources being industrial activity, traffic and agricultural waste burning. Carcinogenic PAHs contribute 44.8-56.4% for 5-20cm and 43.7-55.8% for 0-5cm depth to total PAHs. In some locations the HCH, DDT and PAH amounts exceed the legal values. PMID:23063641

  4. Concentration profiles, source apportionment and risk assessment of polycyclic aromatic hydrocarbons (PAHs) in dumpsite soils from Agbogbloshie e-waste dismantling site, Accra, Ghana.

    PubMed

    Daso, Adegbenro P; Akortia, Eric; Okonkwo, Jonathan O

    2016-06-01

    The concentrations of eighteen (18) polycyclic aromatic hydrocarbons (PAHs), including the 16 USEPA's priority PAHs as well as two alkyl-substituted naphthalenes were determined in dumpsite soils collected from different sampling sites within the Agbogbloshie e-waste dismantling site in Accra, Ghana. Following their isolation with ultrasonic-assisted extraction technique, the concentrations of the PAHs were determined by gas chromatography mass spectrometry (GC-MS). Loss-on-ignition (LOI) method was employed for the determination of total organic carbon (TOC) of the soil samples. The mean Σ18PAHs obtained were 3006, 5627, 3046, 5555, and 7199 ng g(-1) dry weight (dw) for sampling sites A (mosque), B (dismantling site), C (residential house/police station), D (personal computer repairers' shop) and E (e-waste open burning area), respectively. In all cases, the prevalence of phenanthrene, fluoranthene and pyrene was generally observed across the sampling sites. In this study, PAHs with two to three rings and four to six rings exhibited strong positive correlations, whereas BbF and BkF showed weak positive and negative correlations with other PAHs investigated. With the exception of BbF and BkF, all the PAHs had moderate to strong positive correlations with the TOC. Benzo[a]pyrene equivalent (BaPeq) concentration is a useful indicator of the carcinogenic potency of environmental matrices and these ranged between 111 and 454 ng g(-1), which are generally below the 'safe' level of 600 ng g(-1) established for the protection of the environment and human health. Interestingly, the seven carcinogenic PAHs were the major contributors to the BaPeq concentrations accounting between 97.7 and 98.3 %. Despite the minimal risk to cancer via exposure to the investigated dumpsite soil as indicated in the present study, the prolonged exposure to these pollutants via various exposure pathways may result in increased risk to cancer over time. The application of several

  5. [Concentrations and Component Profiles PAHs in Surface Soils and Wheat Grains from the Cornfields Close to the Steel Smelting Industry in Handan, Hebei Province].

    PubMed

    Wu, Di; Wang, Yi-long; Liu, Wei-jian; Chen, Yuan-chen; Fu, Xiao-fang; Tao, Shu; Liu, Wen-xin

    2016-02-15

    In this study, paired surface soil and mature wheat grain samples were collected in the cornfields near the large Handan Steel Manufacturer; and the total concentrations and compositional profiles of the parent PAHs were measured, then the spatial distribution characteristics and correlation with total organic carbon fractions in soil were determined. Accordingly, a preliminary source identification was performed, and the association between PAHs in surface soil and wheat grain was briefly discussed. The median concentration of total PAHs in surface soils from the cornfields of Handan was 398.9 ng x g(-1) (ranged from 123.4 ng x g(-1) to 1626.4 ng x g(-1), where around 18% and 10% of all the studied soil samples were over the corresponding quality criteria for total PAHs and B [a] P in soils, respectively. The MMW and HMW species were the main components in the compositional profiles of surface soils. Based on the specific isomeric ratios of PAHs species, coal/biomass combustion and transportation fuel (tail gas) were the dominant mixed sources for the local PAHs emission. The fractions of surface soil TOC had significant positive correlations with the total PAHs and also with the individual components with different rings. In addition, the median concentration of total PAHs in wheat grains collected in the cornfields near the Handan Steel Manufacture was 27.0 ng x g(-1) (ranged from 19.0-34.0 ng x g(-1)). The levels in wheat grains were not high, and lower than the related hygienic standards of food proposed by EU and China. The LMW and MMW PAHs with 2 to 4 rings occupied a larger proportion, more than 84% of the total PAHs, which was largely different from the component profiles in surface soils. This situation suggested that the local sources of PAHs in wheat grains may originate not only from surface soil via root absorption and internal transportation, but also from ambient air through dry and wet deposition on the leaf surface (stoma). PMID:27363168

  6. Interspecies and interregional comparisons of the chemistry of PAHs and trace elements in mosses Hylocomium splendens (Hedw.) B.S.G. and Pleurozium schreberi (Brid.) Mitt. from Poland and Alaska

    USGS Publications Warehouse

    Migaszewski, Z.M.; Galuszka, A.; Crock, J.G.; Lamothe, P.J.; Dolegowska, S.

    2009-01-01

    Comparative biogeochemical studies performed on the same plant species in remote areas enable pinpointing interspecies and interregional differences of chemical composition. This report presents baseline concentrations of PAHs and trace elements in moss species Hylocomium splendens and Pleurozium schreberi from the Holy Cross Mountains (south-central Poland) (HCM) and Wrangell-Saint Elias National Park and Preserve (Alaska) and Denali National Park and Preserve (Alaska). Total PAH concentrations in the mosses of HCM were in the range of 473-2970 ??g kg-1 (dry weight basis; DW), whereas those in the same species of Alaska were 80-3390 ??g kg-1 DW. Nearly all the moss samples displayed the similar ring sequence: 3 > 4 > 5 > 6 for the PAHs. The 3 + 4 ring/total PAH ratios show statistically significant differences between HCM (0.73) and Alaska (0.91). The elevated concentrations of PAHs observed in some sampling locations of the Alaskan parks were linked to local combustion of wood, with a component of vehicle particle- and vapor-phase emissions. In HCM, the principal source of PAH emissions has been linked to residential and industrial combustion of coal and vehicle traffic. In contrast to HCM, the Alaskan mosses were distinctly elevated in most of the trace elements, bearing a signature of??the underlying geology. H.??splendens and P. schreberi showed diverse bioaccumulative capabilities of PAHs in all three study areas. ?? 2008 Elsevier Ltd.

  7. Carbon in The Universe: PAHs and Clusters

    NASA Technical Reports Server (NTRS)

    Saykally, Richard J.

    1997-01-01

    Following the initial demonstration of this new technique (Science 265 1686 (1994)) and its application to a series of neutral PAHs which have been proposed as condidates for the UIRs (Nature 380, 227 (1996)), we have concentrated on two major aspects of this project. 1. Developing a detailed model for infrared emission spectra of a collection of highly excited PAH molecules, in which experimental bandshapes and temperature-dependent redshifts are used in conjunction with ab initio vibrational frequencies and intensities to simulate the UIR bands. This shows that a collection of nine different cations (as large as ovalene) reproduce the UIR features better than do a collection of the corresponding neutrals, but a detailed match with the UIRs is not obtained. 2. Construction of SPIRES apparatus for the study of PAH ion emission spectra. The design of this experiment is shown and described. Unfortunately a disasterous accident occurred just as we were preparing to start the testing of the ion apparatus. A vacuum implosion occurred, destroying the liquid He cooled monochromator. It has taken us nearly one full year to reconstruct this, and we arc only now in the final testing of the new system. We expect to try the ion experiments by the end of summer.

  8. Interactions between manganese oxides and multiple-ringed aromatic compounds

    SciTech Connect

    Whelan, G. ); Sims, R.C. . Dept. of Civil and Environmental Engineering)

    1992-08-01

    Objective is to determine whether Mn reductive dissolution can oxidize multiple-ringed aromatics, such as PAHs, in an oxic environment Research indicated that certain PAHs (eg, dihydrodiols and diones that form free-radical intermediates) are susceptible to oxidation and polymerization. Over 14 days, 83, 76, 54, 70, and 20% of the Mn was reduced by 2,3-, 1,3-, and 1,4-naphthalenediol, quinizarin, and 1,4-naphthoquinone, respectively. 100, 100, and 65% of the first three PAHs were oxidized, respectively. Aromatics with diol functional groups were more easily oxidized than those with only dione groups. Relatively insoluble compounds like quinizarin can be oxidized; insoluble ''humic-like'' material precipitated, indicating a polymerization-humification process. Results suggest that electron transfer/organic release from the oxide surface is the rate-limiting step.

  9. Interactions between manganese oxides and multiple-ringed aromatic compounds

    SciTech Connect

    Whelan, G.; Sims, R.C.

    1992-08-01

    Objective is to determine whether Mn reductive dissolution can oxidize multiple-ringed aromatics, such as PAHs, in an oxic environment? Research indicated that certain PAHs (eg, dihydrodiols and diones that form free-radical intermediates) are susceptible to oxidation and polymerization. Over 14 days, 83, 76, 54, 70, and 20% of the Mn was reduced by 2,3-, 1,3-, and 1,4-naphthalenediol, quinizarin, and 1,4-naphthoquinone, respectively. 100, 100, and 65% of the first three PAHs were oxidized, respectively. Aromatics with diol functional groups were more easily oxidized than those with only dione groups. Relatively insoluble compounds like quinizarin can be oxidized; insoluble ``humic-like`` material precipitated, indicating a polymerization-humification process. Results suggest that electron transfer/organic release from the oxide surface is the rate-limiting step.

  10. Bis(2,4,6-tri-amino-pyrimidin-1-ium) sulfate penta-hydrate.

    PubMed

    Nimthong, Ruthairat; Chamchong, Siva; Pakawatchai, Chaveng; Mokhagul, Jedsada; Wattanakanjana, Yupa

    2013-01-01

    The asymmetric unit of the title salt, 2C4H8N5 (+)·SO4 (2-)·5H2O, contains four 2,4,6-tri-amino-pyrimidinium (TAPH(+)) cations, two sulfate anions and ten lattice water mol-ecules. Each two of the four TAPH(+) cations form dimers via N-H⋯N hydrogen bonds between the amino groups and the unprotonated pyrimidine N atoms [graph-set motif R 2 (2)(8)]. The (TAPH(+))2 dimers, in turn, form slightly offset infinite π-π stacks parallel to [010], with centroid-centroid distances between pyrimidine rings of 3.5128 (15) and 3.6288 (16) Å. Other amino H atoms, as well as the pyrimidinium N-H groups, are hydrogen-bonded to sulfate and lattice water O atoms. The SO4 (2-) anions and water mol-ecules are inter-connected with each other via O-H⋯O hydrogen bonds. The combination of hydrogen-bonding inter-actions and π-π stacking leads to the formation of a three-dimensional network with alternating columns of TAPH(+) cations and channels filled with sulfate anions and water mol-ecules. One of the sulfate anions shows a minor disorder by a ca 37° rotation around one of the S-O bonds [occupancy ratio of the two sets of sites 0.927 (3):0.073 (3)]. One water mol-ecule is disordered over two mutually exclusive positions with an occupancy ratio of 0.64 (7):0.36 (7). PMID:24109349

  11. Comparative developmental toxicity of environmentally relevant oxygenated PAHs

    PubMed Central

    Knecht, Andrea L.; Goodale, Britton C.; Truong, Lisa; Simonich, Michael T.; Swanson, Annika J.; Matzke, Melissa M.; Anderson, Kim A.; Waters, Katrina M.; Tanguay, Robert L.

    2014-01-01

    Oxygenated polycyclic aromatic hydrocarbons (OPAHs) are byproducts of combustion and photo-oxidation of parent PAHs. OPAHs are widely present in the environment and pose an unknown hazard to human health. The developing zebrafish was used to evaluate a structurally diverse set of 38 OPAHs for malformation induction, gene expression changes and mitochondrial function. Zebrafish embryos were exposed from 6 to 120 h post fertilization (hpf) to a dilution series of 38 different OPAHs and evaluated for 22 developmental endpoints. AHR activation was determined via CYP1A immunohistochemistry. Phenanthrenequinone (9,10-PHEQ), 1,9-benz-10-anthrone (BEZO), xanthone (XAN), benz(a)anthracene-7,12-dione (7,12-B[a]AQ), and 9,10-anthraquinone (9,10-ANTQ) were evaluated for transcriptional responses at 48 hpf, prior to the onset of malformations. qRT-PCR was conducted for a number of oxidative stress genes, including the glutathione transferase(gst), glutathione peroxidase(gpx), and superoxide dismutase(sod) families. Bioenergetics was assayed to measure in vivo oxidative stress and mitochondrial function in 26 hpf embryos exposed to OPAHs. Hierarchical clustering of the structure-activity outcomes indicated that the most toxic of the OPAHs contained adjacent diones on 6-carbon moieties or terminal, para-diones on multi-ring structures. 5-carbon moieties with adjacent diones were among the least toxic OPAHs while the toxicity of multi-ring structures with more centralized para-diones varied considerably. 9,10-PHEQ, BEZO, 7,12-B[a]AQ, and XAN exposures increased expression of several oxidative stress related genes and decreased oxygen consumption rate (OCR), a measurement of mitochondrial respiration. Comprehensive in vivo characterization of 38 structurally diverse OPAHs indicated differential AHR dependency and a prominent role for oxidative stress in the toxicity mechanisms. PMID:23684558

  12. Vibrational spectra of four polycyclic aromatic hydrocarbons under high pressure: implications for stabilities of PAHs during accretion

    NASA Astrophysics Data System (ADS)

    O'Bannon, Earl; Williams, Quentin

    2016-03-01

    Infrared and Raman spectra of the polycyclic aromatic hydrocarbons (PAHs) naphthalene, anthracene, phenanthrene, and pyrene have been examined up to 10-55 GPa at 300 K, to probe structural changes in these materials under high-pressures, and to relate these to shock measurements on these materials. The goal is to develop an understanding of how such hydrocarbons might be processed during planetary accretion. A range of phase transitions in PAHs are observed and, in accord with previous investigations, these typically initiate at relatively low pressures (0.3-4.0 GPa): the lower-pressure transitions are likely associated with inter-molecular changes such as changes in symmetry and/or molecular orientation, charge transfer processes, or changes in π electron density, and are often sluggish. Higher-pressure (7-10 GPa) phase transitions in PAHs are likely associated with profound structural changes like dimerization, which are not always reversible. Laser-induced luminescence is encountered at pressures well below those at which PAHs amorphize, and a strong pressure-induced Fermi resonance is identified between the highest-lying inter-molecular modes and lowest-lying intra-molecular modes in each PAH examined. It is the increased strength of inter-molecular interactions under pressure that likely generates increasing overlap of π orbitals and leads to cross-linking (dimerization) of the molecules and the destruction of their planar symmetry. The first step in the amorphization of these compounds is likely dimerization, and amorphization occurs when long-range order is lost and a greater diversity of local structural environments is introduced into these materials, such as carbons being shared between rings, embayed structures, sp, sp2, and sp3 hybridized carbon atoms, a broad range of C-H bonding environments, and fewer residual resonance-stabilized C-C units. Our results are consistent with pressure producing amorphous, hydrogenated carbon material from PAH

  13. PAH concentrations in the moss species Hylocomium splendens (Hedw.) B.S.G. and Pleurozium schreberi (Brid.) Mitt. from the Kielce area (south-central Poland).

    PubMed

    Dołęgowska, Sabina; Migaszewski, Zdzisław M

    2011-09-01

    Forty eight samples of mosses Hylocomium splendens and Pleurozium schreberi from the Kielce area (south-central Poland) were analyzed for seventeen polycyclic aromatic hydrocarbons. The PAH concentrations varied from 558.00 μg/kg (ppb) to 4457.00 μg/kg in H. splendens and from 643.00 to 3086.00 μg/kg in P. schreberi. In both moss species phenanthrene (75.00-732.00 μg/kg), fluoranthene (101.00-577.00 μg/kg) and pyrene (68.00-568.00 μg/kg) predominated, but H. splendens accumulated more PAHs than P. schreberi at eighteen different sites. The highest PAH concentrations were noted at sites located close to the housing estates (sites 1-10) and potential emission sources (e.g. heat and power generating plant "Kielce S.A.") (sites 19-21). The moss samples displayed the diverse ring sequence, but the most prevalent was four>five>three>six. The diagnostic ratios (three+four ring/total PAHs, Flu/Py, Phen/Ant, Phen/Phen+Ant, Flu/Flu+Py, IndPy/IndPy+BghiPe and BaA/BaA+Chr) indicated that coal and petroleum combustion was a principal PAH source in the study area. PMID:21652075

  14. Mitigation of PAH and nitro-PAH emissions from nonroad diesel engines.

    PubMed

    Liu, Z Gerald; Wall, John C; Ottinger, Nathan A; McGuffin, Dana

    2015-03-17

    More stringent emission requirements for nonroad diesel engines introduced with U.S. Tier 4 Final and Euro Stage IV and V regulations have spurred the development of exhaust aftertreatment technologies. In this study, several aftertreatment configurations consisting of diesel oxidation catalysts (DOC), diesel particulate filters (DPF), Cu zeolite-, and vanadium-based selective catalytic reduction (SCR) catalysts, and ammonia oxidation (AMOX) catalysts are evaluated using both Nonroad Transient (NRTC) and Steady (8-mode NRSC) Cycles in order to understand both component and system-level effects of diesel aftertreatment on emissions of polycyclic aromatic hydrocarbons (PAH) and their nitrated derivatives (nitro-PAH). Emissions are reported for four configurations including engine-out, DOC+CuZ-SCR+AMOX, V-SCR+AMOX, and DOC+DPF+CuZ-SCR+AMOX. Mechanisms responsible for the reduction, and, in some cases, the formation of PAH and nitro-PAH compounds are discussed in detail, and suggestions are provided to minimize the formation of nitro-PAH compounds through aftertreatment design optimizations. Potency equivalency factors (PEFs) developed by the California Environmental Protection Agency are then applied to determine the impact of aftertreatment on PAH-derived exhaust toxicity. Finally, a comprehensive set of exhaust emissions including criteria pollutants, NO2, total hydrocarbons (THC), n-alkanes, branched alkanes, saturated cycloalkanes, aromatics, aldehydes, hopanes and steranes, and metals is provided, and the overall efficacy of the aftertreatment configurations is described. This detailed summary of emissions from a current nonroad diesel engine equipped with advanced aftertreatment can be used to more accurately model the impact of anthropogenic emissions on the atmosphere. PMID:25668360

  15. Evaluation of poly-aromatic hydrocarbons (PAHs) in the aquatic species of Suez Gulf water along El-Sokhna area to the Suez refineries.

    PubMed

    Ali, Nabila A; Ahmed, Omayma E; Doheim, Mamdouh M

    2014-02-01

    The Egyptian Red Sea environment especially along El-Sokhna area to the Suez refineries (Suez) is severely contaminated with organic compounds, as well as overfishing. This may be well contributory to recent serious declines in fish stocks. Fish embryos are also particularly vulnerable to oil exposure, even at extremely low concentrations of less than one part per billion. Consequently, even traces of oil pollution at levels often considered safe for wildlife can cause severe damage to fish. Sixteen polycyclic aromatic hydrocarbons (PAHs) were investigated in ten fish species of aquatic species by high performance liquid chromatography (HPLC). The compositions of PAHs determined in all samples were measured in order to use them as chemical markers for identifying different sources of PAH pollutants in the studied region. The total content of these16 PAHs ranged from 399.616 up to 67,631.779 ng/g wet weight. The data show that these values are considered to be alarmingly high enough to cause lethal toxicity effect by accumulation. All studied aquatic species samples are characterized by relatively high concentrations of the six-membered ring PAHs. The origin of PAHs in the collected samples is either petrogenic, biogenic, or mixed petrogenic and biogenic. PMID:24092254

  16. The relative abundance and seasonal distribution correspond with the sources of polycyclic aromatic hydrocarbons (PAHs) in the surface sediments of Chenab River, Pakistan.

    PubMed

    Hussain, Imran; Syed, Jabir Hussain; Kamal, Atif; Iqbal, Mehreen; Eqani, Syed-Ali-Mustjab-Akbar-Shah; Bong, Chui Wei; Taqi, Malik Mumtaz; Reichenauer, Thomas G; Zhang, Gan; Malik, Riffat Naseem

    2016-06-01

    Chenab River is one of the most important rivers of Punjab Province (Pakistan) that receives huge input of industrial effluents and municipal sewage from major cities in the Central Punjab, Pakistan. The current study was designed to evaluate the concentration levels and associated ecological risks of USEPA priority polycyclic aromatic hydrocarbons (PAHs) in the surface sediments of Chenab River. Sampling was performed from eight (n = 24) sampling stations of Chenab River and its tributaries. We observed a relatively high abundance of ∑16PAHs during the summer season (i.e. 554 ng g(-1)) versus that in the winter season (i.e. 361 ng g(-1)), with an overall abundance of two-, five- and six-ring PAH congeners. Results also revealed that the nitrate and phosphate contents in the sediments were closely associated with low molecular weight (LMW) and high molecular weight (HMW) PAHs, respectively. Source apportionment results showed that the combustion of fossil fuels appears to be the key source of PAHs in the study area. The risk quotient (RQ) values indicated that seven PAH congeners (i.e. phenanthrene, anthracene, fluoranthene, pyrene, benzo(a)pyrene, chrysene and benzo(a)anthracene) could pose serious threats to the aquatic life of the riverine ecosystem in Pakistan. PMID:27234513

  17. Ringing wormholes

    SciTech Connect

    Konoplya, R.A.; Molina, C.

    2005-06-15

    We investigate the response of traversable wormholes to external perturbations through finding their characteristic frequencies and time-domain profiles. The considered solution describes traversable wormholes between the branes in the two brane Randall-Sundrum model and was previously found within Einstein gravity with a conformally coupled scalar field. The evolution of perturbations of a wormhole is similar to that of a black hole and represents damped oscillations (ringing) at intermediately late times, which are suppressed by power-law tails (proportional to t{sup -2} for monopole perturbations) at asymptotically late times.

  18. Field-based evaluation of semipermeable membrane devices (SPMDs) as passive air samplers of polyaromatic hydrocarbons (PAHs)

    NASA Astrophysics Data System (ADS)

    Bartkow, Michael E.; Huckins, James N.; Müller, Jochen F.

    2004-11-01

    Semipermeable membrane devices (SPMDs) have been used as passive air samplers of semivolatile organic compounds in a range of studies. However, due to a lack of calibration data for polyaromatic hydrocarbons (PAHs), SPMD data have not been used to estimate air concentrations of target PAHs. In this study, SPMDs were deployed for 32 days at two sites in a major metropolitan area in Australia. High-volume active sampling systems (HiVol) were co-deployed at both sites. Using the HiVol air concentration data from one site, SPMD sampling rates were measured for 12 US EPA Priority Pollutant PAHs and then these values were used to determine air concentrations at the second site from SPMD concentrations. Air concentrations were also measured at the second site with co-deployed HiVols to validate the SPMD results. PAHs mostly associated with the vapour phase (Fluorene to Pyrene) dominated both the HiVol and passive air samples. Reproducibility between replicate passive samplers was satisfactory (CV<20%) for the majority of compounds. Sampling rates ranged between 0.6 and 6.1 m3 d-1. SPMD-based air concentrations were calculated at the second site for each compound using these sampling rates and the differences between SPMD-derived air concentrations and those measured using a HiVol were, on average, within a factor of 1.5. The dominant processes for the uptake of PAHs by SPMDs were also assessed. Using the SPMD method described herein, estimates of particulate sorbed airborne PAHs with five rings or greater were within 1.8-fold of HiVol measured values.

  19. Monitoring of Long-Term Outdoor Concentrations of PAHs with Passive Air Samplers and Comparison with Meteorological Data.

    PubMed

    Evci, Y Mine; Esen, Fatma; Taşdemir, Yücel

    2016-08-01

    The passive air sampler (PAS) is a common and useful tool for the sampling of semivolatile organic compounds in the ambient air. In a study performed in a semirural area of Bursa, sampling of polycyclic aromatic hydrocarbons (PAHs), was completed between February 4, 2013, and February 3, 2014, during 10-, 20-, 30-, 40- and 60 day periods for 1 year. To determine polycyclic aromatic compounds (PAH) concentrations, 3 PASs and 1 high-volume air sampler were run simultaneously, and sampling rates (R [m(3)/d]) were calculated seasonally and according to the ring numbers of the PAHs. R values varied from 0.66 to 22.41 m(3)/d. The relationship of these values with meteorological conditions was examined statistically, and the regressions performed were found to be consistent. This study identified 15 PAH compounds [Formula: see text]. Concentration values of 10 day samples fluctuated from 6.4 to 1100 ng/m(3). Seasonal averages of the concentrations of ∑15PAHs were detected to be 141 ± 72.5 ng/m(3) for winter, 74 ± 59 ng/m(3) for spring, 7 ± 0.6 ng/m(3) for summer and 840 ± 170 ng/m(3) for autumn. In this study, the toxicity equivalents of seasonal PAH concentrations obtained were determined to be 0.5, 0.3, 0.1, and 1.8 ng/m(3) in winter, spring, summer and fall, respectively. The type posing a cancer risk has been identified as BaA. PMID:27300346

  20. Field-based evaluation of semipermeable membrane devices (SPMDs) as passive air samplers of polyaromatic hydrocarbons (PAHs)

    USGS Publications Warehouse

    Bartkow, M.E.; Huckins, J.N.; Muller, J.F.

    2004-01-01

    Semipermeable membrane devices (SPMDs) have been used as passive air samplers of semivolatile organic compounds in a range of studies. However, due to a lack of calibration data for polyaromatic hydrocarbons (PAHs), SPMD data have not been used to estimate air concentrations of target PAHs. In this study, SPMDs were deployed for 32 days at two sites in a major metropolitan area in Australia. High-volume active sampling systems (HiVol) were co-deployed at both sites. Using the HiVol air concentration data from one site, SPMD sampling rates were measured for 12 US EPA Priority Pollutant PAHs and then these values were used to determine air concentrations at the second site from SPMD concentrations. Air concentrations were also measured at the second site with co-deployed HiVols to validate the SPMD results. PAHs mostly associated with the vapour phase (Fluorene to Pyrene) dominated both the HiVol and passive air samples. Reproducibility between replicate passive samplers was satisfactory (CV<20%) for the majority of compounds. Sampling rates ranged between 0.6 and 6.1 m3 d-1. SPMD-based air concentrations were calculated at the second site for each compound using these sampling rates and the differences between SPMD-derived air concentrations and those measured using a HiVol were, on average, within a factor of 1.5. The dominant processes for the uptake of PAHs by SPMDs were also assessed. Using the SPMD method described herein, estimates of particulate sorbed airborne PAHs with five rings or greater were within 1.8-fold of HiVol measured values. ?? 2004 Elsevier Ltd. All rights reserved.

  1. Biotransformation of the high-molecular weight polycyclic aromatic hydrocarbon (PAH) benzo[k]fluoranthene by Sphingobium sp. strain KK22 and identification of new products of non-alternant PAH biodegradation by liquid chromatography electrospray ionization tandem mass spectrometry

    PubMed Central

    Maeda, Allyn H; Nishi, Shinro; Hatada, Yuji; Ozeki, Yasuhiro; Kanaly, Robert A

    2014-01-01

    A pathway for the biotransformation of the environmental pollutant and high-molecular weight polycyclic aromatic hydrocarbon (PAH) benzo[k]fluoranthene by a soil bacterium was constructed through analyses of results from liquid chromatography negative electrospray ionization tandem mass spectrometry (LC/ESI(–)-MS/MS). Exposure of Sphingobium sp. strain KK22 to benzo[k]fluoranthene resulted in transformation to four-, three-and two-aromatic ring products. The structurally similar four-and three-ring non-alternant PAHs fluoranthene and acenaphthylene were also biotransformed by strain KK22, and LC/ESI(–)-MS/MS analyses of these products confirmed the lower biotransformation pathway proposed for benzo[k]fluoranthene. In all, seven products from benzo[k]fluoranthene and seven products from fluoranthene were revealed and included previously unreported products from both PAHs. Benzo[k]fluoranthene biotransformation proceeded through ortho-cleavage of 8,9-dihydroxy-benzo[k]fluoranthene to 8-carboxyfluoranthenyl-9-propenic acid and 9-hydroxy-fluoranthene-8-carboxylic acid, and was followed by meta-cleavage to produce 3-(2-formylacenaphthylen-1-yl)-2-hydroxy-prop-2-enoic acid. The fluoranthene pathway converged with the benzo[k]fluoranthene pathway through detection of the three-ring product, 2-formylacenaphthylene-1-carboxylic acid. Production of key downstream metabolites, 1,8-naphthalic anhydride and 1-naphthoic acid from benzo[k]fluoranthene, fluoranthene and acenaphthylene biotransformations provided evidence for a common pathway by strain KK22 for all three PAHs through acenaphthoquinone. Quantitative analysis of benzo[k]fluoranthene biotransformation by strain KK22 confirmed biodegradation. This is the first pathway proposed for the biotransformation of benzo[k]fluoranthene by a bacterium. PMID:24325265

  2. Distribution of polycyclic aromatic hydrocarbons (PAH's) in marsh sediments, Iraq

    SciTech Connect

    Al-Saad, H.T.; Al-Timari, A.A. )

    1989-12-01

    Recently there has been a growing concern in the release of harmful organics into the environment. Carcinogenic polycyclic aromatic hydrocarbons (PAH's) are a class of compounds of interset due to their possible harmful effects to man as well as organisms. Anthropogenic PAH's may reach aquatic environment as a result of both industrial and domestic effluents, deposition of airborne particles, surface runoff and oil spillage. Having a relatively low water solubility and high affinity to sorb to the suspended particulate matter, most of the PAH's introduced to the aquatic environment tend to accumulate in bottom sediments. Sedimentary PAH's may thus provide a record of the input and history of these pollutants. Consequently, the distribution of PAH's in aquatic sediments have received considerable attention. The purpose of the present work was to establish the distribution of PAH's in the sediments of the marsh region located in southern Iraq.

  3. 26 CFR 1.401(a)(4)-6 - Contributory defined benefit plans.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 26 Internal Revenue 5 2011-04-01 2011-04-01 false Contributory defined benefit plans. 1.401(a)(4)-6 Section 1.401(a)(4)-6 Internal Revenue INTERNAL REVENUE SERVICE, DEPARTMENT OF THE TREASURY (CONTINUED) INCOME TAX (CONTINUED) INCOME TAXES (CONTINUED) Pension, Profit-Sharing, Stock Bonus Plans, Etc. § 1.401(a)(4)-6 Contributory defined...

  4. Preliminary study of children's exposure to PAHs and its association with 8-hydroxy-2'-deoxyguanosine in Guangzhou, China.

    PubMed

    Fan, Ruifang; Wang, Dongli; Mao, Chuanwei; Ou, Shangkang; Lian, Zhixia; Huang, Shaoling; Lin, Qiongshan; Ding, Runhao; She, Jianwen

    2012-07-01

    Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous air pollutants generated mainly from incomplete combustion such as automobile exhaust and cigarette smoke. Oxidative stress is believed to be involved in carcinogenesis, and urinary 8-hydroxy-2'-deoxyguanosine (8-OHdG) was used as the biomarker to assess such DNA damage. The children's urinary PAH metabolite (OH-PAHs) level were explored in Guangzhou and their associations with 8-OHdG. Two groups of subjects were selected: (1) one group (n=39, 6-7 years old) from an elementary school situated near a heavy traffic road (polluted area) and (2) another group (n=35, 4-6 years old) from a kindergarten situated in a corner of the main campus of a big university (non-polluted area). Urinary 8-OHdG and nine urinary monohydroxylated PAH metabolites were measured, including 2-hydroxynaphthalene (2-OHN), 2-hydroxyfluorene (2-OHF), 2-, 3-, 4-, 9-hydroxyphenanthrene (2-, 3-, 4-, 9-OHPhe), 1-hydroxypyrene (1-OHP), 6-hydroxychrysene (6-OHChr) and 3-hydroxybenzo(a)pyrene (3-OHBaP). All other PAH metabolites were detected in urine samples from both children groups except for 6-OHChr and 3-OHBaP. Levels of 2-OHN, 2-OHF, 3-OHPhe, 9-OHPhe and 1-OHP were significantly different between two groups (P<0.05, T-test). The elementary school children from the polluted area had higher urinary levels of 2-OHN, 2-OHF, 2-, 3-, 4-OHPhe and 1-OHP ((9.10±7.39, 3.72±2.91, 0.32±0.50, 0.37±0.28, 0.23±0.29 and 0.64±0.07 μmol/mol creatinine, respectively) than those from the control group. The results suggested that heavy traffic pollution led to higher PAH body burden. There existed no significant difference for urinary 8-OHdG concentration between two groups (p>0.05, T-test), and no strong correlations between the individual OH-PAHs and 8-OHdG. However, the urinary 8-OHdG concentration in the elementary school children from the traffic polluted area was slightly higher than those in the non-polluted area (20.87±14.42 μmol/mol creatinine

  5. Recombination Rates of Electrons with Interstellar PAH Molecules

    NASA Technical Reports Server (NTRS)

    Ballester, Jorge (Cartographer)

    1996-01-01

    The goal of this project is to develop a general model for the recombination of electrons with PAH molecules in an interstellar environment. The model is being developed such that it can be applied to a small number of families of PAHs without reference to specific molecular structures. Special attention will be focused on modeling the approximately circular compact PAHs in a way that only depends on the number of carbon atoms.

  6. Ligand-specific transcriptional mechanisms underlie aryl hydrocarbon receptor-mediated developmental toxicity of oxygenated PAHs

    SciTech Connect

    Goodale, B. C.; La Du, J.; Tilton, S. C.; Sullivan, C. M.; Bisson, W. H.; Waters, K. M.; Tanguay, R. L.

    2015-07-03

    Polycyclic aromatic hydrocarbons (PAHs) are priority environmental contaminants that exhibit mutagenic, carcinogenic, proinflammatory, and teratogenic properties. Oxygen-substituted PAHs (OPAHs) are formed during combustion processes and via phototoxidation and biological degradation of parent (unsubstituted) PAHs. Despite their prevalence both in contaminated industrial sites and in urban air, OPAH mechanisms of action in biological systems are relatively understudied. Like parent PAHs, OPAHs exert structure-dependent mutagenic activities and activation of the aryl hydrocarbon receptor (AHR) and cytochrome p450 metabolic pathway. Four-ring OPAHs 1,9-benz-10-anthrone (BEZO) and benz(a)anthracene-7,12-dione (7,12-B[a]AQ) cause morphological aberrations and induce markers of oxidative stress in developing zebrafish with similar potency, but only 7,12-B[a]AQ induces robust Cyp1a protein expression. We investigated the role of the AHR in mediating the toxicity of BEZO and 7,12-B[a]AQ, and found that knockdown of AHR2 rescued developmental effects caused by both compounds. Using RNA-seq and molecular docking, we identified transcriptional responses that precede developmental toxicity induced via differential interaction with AHR2. Redox-homeostasis genes were affected similarly by these OPAHs, while 7,12-B[a]AQ preferentially activated phase 1 metabolism and BEZO uniquely decreased visual system genes. Analysis of biological functions and upstream regulators suggests that BEZO is a weak AHR agonist, but interacts with other transcriptional regulators to cause developmental toxicity in an AHR-dependent manner. Furthermore, identifying ligand-dependent AHR interactions and signaling pathways is essential for understanding toxicity of this class of environmentally relevant compounds.

  7. Ligand-specific transcriptional mechanisms underlie aryl hydrocarbon receptor-mediated developmental toxicity of oxygenated PAHs

    DOE PAGESBeta

    Goodale, B. C.; Geisel School of Medicine at Dartmouth, Hanover, NH; La Du, J.; Tilton, S. C.; Pacific Northwest National Lab.; Sullivan, C. M.; Bisson, W. H.; Waters, K. M.; Tanguay, R. L.

    2015-07-03

    Polycyclic aromatic hydrocarbons (PAHs) are priority environmental contaminants that exhibit mutagenic, carcinogenic, proinflammatory, and teratogenic properties. Oxygen-substituted PAHs (OPAHs) are formed during combustion processes and via phototoxidation and biological degradation of parent (unsubstituted) PAHs. Despite their prevalence both in contaminated industrial sites and in urban air, OPAH mechanisms of action in biological systems are relatively understudied. Like parent PAHs, OPAHs exert structure-dependent mutagenic activities and activation of the aryl hydrocarbon receptor (AHR) and cytochrome p450 metabolic pathway. Four-ring OPAHs 1,9-benz-10-anthrone (BEZO) and benz(a)anthracene-7,12-dione (7,12-B[a]AQ) cause morphological aberrations and induce markers of oxidative stress in developing zebrafish with similar potency, butmore » only 7,12-B[a]AQ induces robust Cyp1a protein expression. We investigated the role of the AHR in mediating the toxicity of BEZO and 7,12-B[a]AQ, and found that knockdown of AHR2 rescued developmental effects caused by both compounds. Using RNA-seq and molecular docking, we identified transcriptional responses that precede developmental toxicity induced via differential interaction with AHR2. Redox-homeostasis genes were affected similarly by these OPAHs, while 7,12-B[a]AQ preferentially activated phase 1 metabolism and BEZO uniquely decreased visual system genes. Analysis of biological functions and upstream regulators suggests that BEZO is a weak AHR agonist, but interacts with other transcriptional regulators to cause developmental toxicity in an AHR-dependent manner. Furthermore, identifying ligand-dependent AHR interactions and signaling pathways is essential for understanding toxicity of this class of environmentally relevant compounds.« less

  8. Regional-scale simulation of transport and transformations of semi-volatile polycyclic aromatic hydrocarbons (PAHs) in East Asia: diurnal variations investigation

    NASA Astrophysics Data System (ADS)

    Mu, Qing; Lammel, Gerhard; Cheng, Yafang

    2015-04-01

    Semi-volatile PAHs are major pollutants of urban air, mostly regionally transported and reaching remote environments[1]. Some semi-volatile PAHs are carcinogenic. About 22% of global PAHs emissions are in China. The transport and sinks (atmospheric reactions, deposition) of semi-volatile PAHs in East Asia are studied using a modified version of the Weather Research and Forecasting model coupled with chemistry (WRF/Chem [2]). For this purpose, PAHs' gas and particulate phase chemical reactions and dry and wet deposition processes are included. We use emissions of 2008 [3] which include technical combustion processes (coal, oil, gas, waste and biomass) and open fires and apply diurnal time functions as those of black carbon. The model was run for phenanthrene (3-ring PAH, p = 1.5×10-2 Pa at 298 K) and benzo(a)pyrene (5-ring PAH, p = 7×10-7 Pa) for July 2013 with hourly output and 27 km horizontal grid spacing. The comparison of model predicted phenanthrene concentrations with measurements at a rural site near Beijing (own data, unpublished) validates the model's ability to simulate diurnal variations of gaseous PAHs. The model's performance is better in simulating day time than night time gaseous PAHs. The concentrations of PAHs had experienced significant diurnal variations in rural and remote areas of China. Elevated concentration levels of 40-60 ng m-3 for phenanthrene and 1-10 ng m-3 for benzo(a)pyrene are predicted in Shanxi, Guizhou, the North China Plain, the Sichuan Basin and Chongqing metropolitan areas due to the high emission densities at those locations. References [1] Keyte, I.J., Harrison, R.M., and Lammel, G., 2013: Chemical reactivity and long-range transport potential of polycyclic aromatic hydrocarbons - a review, Chem. Soc. Rev., 42, 9333-9391. [2] Grell, G.A, Peckham, S.E, Schmitz, R, McKeen, S.A, Frost, G, Skamarock, W.C, and Eder, B., 2005: Fully coupled online chemistry within the WRF model, Atmos. Environ., 39, 6957-6975. [3] Shen, H. Z

  9. Grafted cellulose for PAHs removal present in industrial discharge waters

    NASA Astrophysics Data System (ADS)

    Euvrard, Elise; Druart, Coline; Poupeney, Amandine; Crini, Nadia; Vismara, Elena; Lanza, Tommaso; Torri, Giangiacomo; Gavoille, Sophie; Crini, Gregorio

    2014-05-01

    Keywords: cellulose; biosorbent; PAHs; polycontaminated wastewaters; trace levels. Polycyclic aromatic hydrocarbons (PAHs), chemicals essentially formed during incomplete combustion of organic materials from anthropogenic activities, were present in all compartments of the ecosystem, air, water and soil. Notably, a part of PAHs found in aquatic system was introduced through industrial discharge waters. Since the Water Framework Directive has classified certain PAHs as priority hazardous substances, industrials are called to take account this kind of organic pollutants in their global environmental concern. Conventional materials such as activated carbons definitively proved their worth as finishing treatment systems but remained costly. In this study, we proposed to use cellulose grafted with glycidyl methacrylate [1] for the removal of PAHs present in discharge waters of surface treatment industries. Firstly, to develop the device, we worked with synthetic solutions containing 16 PAHs at 500 ng/L. Two types of grafted cellulose were tested over a closed-loop column with a concentration of 4g cellulose/L: cellulose C2 with a hydroxide group and cellulose C4 with an amine group. No PAH was retained by the raw cellulose whereas abatement percentages of PAHs were similar between C2 and C4 (94% and 98%, respectively, for the sum of the 16 PAHs) with an experiment duration of 400 min (corresponding to about 20 cycles through grafted cellulose). Secondly, to determine the shorter time to abate the amount maximum of PAHs through the system, a kinetic was realized from 20 min (one cycle) to 400 min with C4. The steady state (corresponding to about 95% of abatement of the total PAHs) was reached at 160 min. Finally, the system was then tested with real industrial discharge waters containing both mineral and organic compounds. The results indicated that the abatement percentage of PAHs was similar between C2 and C4, corroborating the tests with synthetic solution. In return

  10. 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. PMID:26820781

  11. Unlike PAHs from Exxon Valdez crude oil, PAHs from Gulf of Alaska coals are not readily bioavailable.

    PubMed

    Deepthike, Halambage Upul; Tecon, Robin; Van Kooten, Gerry; Van der Meer, Jan Roelof; Harms, Hauke; Wells, Mona; Short, Jeffrey

    2009-08-01

    In the wake of the 1989 Exxon Valdez oil spill, spatially and temporally spill-correlated biological effects consistent with polycyclic aromatic hydrocarbon (PAH) exposure were observed. Some works have proposed that confounding sources from local source rocks, prominently coals, are the provenance of the PAHs. Representative coal deposits along the southeast Alaskan coast (Kulthieth Formation) were sampled and fully characterized chemically and geologically. The coals have variable but high total organic carbon content technically classifying as coals and coaly shale, and highly varying PAH contents. Even for coals with high PAH content (approximately 4000 ppm total PAHs), a PAH-sensitive bacterial biosensor demonstrates nondetectable bioavailability as quantified, based on naphthalene as a test calibrant. These results are consistent with studies indicating that materials such as coals strongly diminish the bioavailability of hydrophobic organic compounds and support previous work suggesting that hydrocarbons associated with the regional background in northern Gulf of Alaska marine sediments are not appreciably bioavailable. PMID:19731689

  12. Level, potential sources of polycyclic aromatic hydrocarbons (PAHs) in particulate matter (PM10) in Naples

    NASA Astrophysics Data System (ADS)

    Di Vaio, Paola; Cocozziello, Beatrice; Corvino, Angela; Fiorino, Ferdinando; Frecentese, Francesco; Magli, Elisa; Onorati, Giuseppe; Saccone, Irene; Santagada, Vincenzo; Settimo, Gaetano; Severino, Beatrice; Perissutti, Elisa

    2016-03-01

    In Naples, particulate matter PM10 associated with polycyclic aromatic hydrocarbons (PAHs) in ambient air were determined in urban background (NA01) and urban traffic (NA02) sites. The principal objective of the study was to determine the concentration and distribution of PAHs in PM10 for identification of their possible sources (through diagnostic ratio - DR and principal component analysis - PCA) and an estimation of the human health risk (from exposure to airborne TEQ). Airborne PM10 samples were collected on quartz filters using a Low Volume Sampler (LVS) for 24 h with seasonal samples (autumn, winter, spring and summer) of about 15 days each between October 2012 and July 2013. The PM10 mass was gravimetrically determined. The PM10 levels, in all seasons, were significantly higher (P < 0.001) in the urban-traffic site (NA02) than in the urban-background site (NA01). The filters were then extracted with dichloromethane using an ultrasonicator (SONICA) to perform a detailed characterization of 12 priority PAHs proposed by the USEPA, by gas chromatography-mass spectrometer (GC-MS) analysis. The concentration of Benzo[a]Pyrene, BaP (EU and National limit value: 1 ng m-3 in PM10), varied from 0.065 ng m-3 during autumn time to 0.872 ng m-3 in spring time (NA01) and from 0.120 ng m-3 during autumn time to 1.48 ng m-3 of winter time (NA02) with four overshoots. In NA02 the trend of Σ12 PAHs was comparable to NA01 but were observed higher values than NA01. In fact, the mean concentration of Σ12 PAHs, in urban-traffic site was generally 2 times greater than in urban-background site in all the campaigns. PAHs with 5 and 6 ring, many of which are suspected carcinogens or genotoxic agents, (i.e Benzo[a]Pyrene, Indeno[1,2,3-cd]Pyrene, Benzo[b]Fluoranthene, Benzo[k]Fluoranthene and Benzo[g,h,i]Perylene), had a large contribution (∼50-55%) of total PAHs concentration in PM10 in two sites and in each of the campaigns. Diagnostic ratio analysis and PCA suggested a

  13. Pleiotropic and Epistatic Behavior of a Ring-Hydroxylating Oxygenase System in the Polycyclic Aromatic Hydrocarbon Metabolic Network from Mycobacterium vanbaalenii PYR-1

    PubMed Central

    Kweon, Ohgew; Kim, Seong-Jae; Kim, Dae-Wi; Kim, Jeong Myeong; Kim, Hyun-lee; Ahn, Youngbeom; Sutherland, John B.

    2014-01-01

    Despite the considerable knowledge of bacterial high-molecular-weight (HMW) polycyclic aromatic hydrocarbon (PAH) metabolism, the key enzyme(s) and its pleiotropic and epistatic behavior(s) responsible for low-molecular-weight (LMW) PAHs in HMW PAH-metabolic networks remain poorly understood. In this study, a phenotype-based strategy, coupled with a spray plate method, selected a Mycobacterium vanbaalenii PYR-1 mutant (6G11) that degrades HMW PAHs but not LMW PAHs. Sequence analysis determined that the mutant was defective in pdoA2, encoding an aromatic ring-hydroxylating oxygenase (RHO). A series of metabolic comparisons using high-performance liquid chromatography (HPLC) analysis revealed that the mutant had a lower rate of degradation of fluorene, anthracene, and pyrene. Unlike the wild type, the mutant did not produce a color change in culture media containing fluorene, phenanthrene, and fluoranthene. An Escherichia coli expression experiment confirmed the ability of the Pdo system to oxidize biphenyl, the LMW PAHs naphthalene, phenanthrene, anthracene, and fluorene, and the HMW PAHs pyrene, fluoranthene, and benzo[a]pyrene, with the highest enzymatic activity directed toward three-ring PAHs. Structure analysis and PAH substrate docking simulations of the Pdo substrate-binding pocket rationalized the experimentally observed metabolic versatility on a molecular scale. Using information obtained in this study and from previous work, we constructed an RHO-centric functional map, allowing pleiotropic and epistatic enzymatic explanation of PAH metabolism. Taking the findings together, the Pdo system is an RHO system with the pleiotropic responsibility of LMW PAH-centric hydroxylation, and its epistatic functional contribution is also crucial for the metabolic quality and quantity of the PAH-MN. PMID:25070740

  14. Transformation ability of fungi isolated from cork and grape to produce 2,4,6-trichloroanisole from 2,4,6-trichlorophenol.

    PubMed

    Maggi, L; Mazzoleni, V; Fumi, M D; Salinas, M R

    2008-03-01

    The ability of eight fungal strains to transform 2,4,6-trichlorophenol (TCP) to 2,4,6-trichloroanisole (TCA) was studied. These fungi were isolated from cork, belonging to the genera Penicillium, Aspergillus, Trichoderma and Chrysonilia, and from grapes Botrytis cinerea. All, except Chrysonilia, produced TCA when grown directly on cork in the presence of TCP, Aspergillus and Botrytis cinerea being the ones with the highest level of production. It is the first time that Botrytis cinerea, a microorganism often present on grapes and in winery environments, has been shown to transform TCP into TCA. This result can partially explain the wine cork taint before being bottled. PMID:18311620

  15. Composition and Integrity of PAHs, Nitro-PAHs, Hopanes and Steranes In Diesel Exhaust Particulate Matter

    PubMed Central

    Huang, Lei; Bohac, Stanislav V.; Chernyak, Sergei M.; Batterman, Stuart A.

    2013-01-01

    Diesel exhaust particulate matter contains many semivolatile organic compounds (SVOCs) of environmental and health significance. This study investigates the composition, emission rates, and integrity of 25 SVOCs, including polycyclic aromatic hydrocarbons (PAHs), nitro-PAHs (NPAHs), and diesel biomarkers hopanes and steranes. Diesel engine particulate matter (PM), generated using an engine test bench, three engine conditions, and ultra-low sulfur diesel (ULSD), was collected on borosilicate glass fiber filters. Under high engine load, the PM emission rate was 0.102 g/kWh, and emission rate of ΣPAHs (10 compounds), ΣNPAHs (6 compounds), Σhopanes (2 compounds), and Σsteranes (2 compounds) were 2.52, 0.351, 0.02 ~ 2 and 1μg/kWh, respectively. Storage losses were evaluated for three cases: conditioning filters in clean air at 25 °C and 33% relative humidity (RH) for 24 h; storing filter samples (without extraction) wrapped in aluminum foil at 4 °C for up to one month; and storing filter extracts in glass vials capped with Teflon crimp seals at 4 °C for up to six months. After conditioning filters for 24 h, 30% of the more volatile PAHs were lost, but lower volatility NPAHs, hopanes and steranes showed negligible changes. Storing wrapped filters and extracts at 4 °C for up to one month did not lead to significant losses, but storing extracts for five months led to significant losses of PAHs and NPAHs; hopanes and steranes demonstrated greater integrity. These results suggest that even relatively brief filter conditioning periods, needed for gravimetric measurements of PM mass, and extended storage of filter extracts can lead to underestimates of SVOC concentrations. Thus, SVOC sampling and analysis protocols should utilize stringent criteria and performance checks to identify and limit possible biases occurring during filter and extract processing. PMID:24363468

  16. Optimization of Polycyclic Aromatic Hydrocarbon (PAH) Extraction Efficiency Parameters for Sub- and Supercritical Water Extraction (SCWE) Instrument

    NASA Technical Reports Server (NTRS)

    Okada, Asahi A.

    2005-01-01

    Polycyclic aromatic hydrocarbons are a class of molecules composed of multiple, bonded benzene rings. As PAHS are believed to be present on Mars, positive confirmation of their presence on Mars is highly desirable. To extract PAHS, which have low volatility, a fluid extraction method is ideal, and one that does not utilize organic solvents is especially ideal for in situ instrumental analysis. The use of water as a solvent, which at subcritical pressures and temperatures is relatively non-Polar, has significant potential. As SCWE instruments have not yet been commercialized, all instruments are individually-built research prototypes: thus, initial efforts were intended to determine if extraction efficiencies on the JPL-built laboratory-scale SCWE instrument are comparable to differing designs built elsewhere. Samples of soil with certified reference concentrations of PAHs were extracted using SCWE as well as conventional Soxhlet extraction. Continuation of the work would involve extractions on JPL'S newer, portable SCWE instrument prototype to determine its efficiency in extracting PAHs.

  17. Synthesis, characterization and in silico biological activity of some 2-(N,N-dimethyl guanidinyl)-4,6-diaryl pyrimidines

    PubMed Central

    Kumarachari, Rajasekhar Komarla; Peta, Sivakumar; Surur, Abdrrahman Shemsu; Mekonnen, Yenus Tadesse

    2016-01-01

    Introduction: As pyrimidine is a basic nucleus in DNA and RNA, it has been found to be associated with diverse biological activities. Pyrimidine derivatives were reported to possess anticonvulsant, antimicrobial, anti-inflammatory, antitumor, and antihistaminic. Recently, our team reported the anti-inflammatory and antimicrobial evaluation of some pyrimidines. Objective: To synthesize, predict and evaluate biological activity of some 2-(N,N-dimethyl guanidinyl)-4,6-diaryl pyrimidines. Experimental: seven new pyrimidines were synthesized by following the standard procedures using substituted aromatic aldehydes, methyl ketones and metformin. After the biological activity was predicted using PASS, Molinspiration and Osiris property explorer, their anthelmintic activity was evaluated using Pheretima posthuma. The structural assignment of the title compounds (P1-7) has been made on the basis of elemental analysis, infrared, 1H-nuclear magnetic resonance and Mass spectral studies. Results: All the synthesized compounds were found to obey Lipinski's rule. All the synthesized compounds scored good bioactivity values as GPCR ligands and kinase inhibitors. Among the test compounds, P5 was found to be more potent anthelmintic inducing paralysis in 36-48 minutes and death in 40-51 minutes. Conclusion and Recommendation: The synthesized compound (P5) possessing methoxy group at position-4 of the benzene ring located at position-4 of pyrimidine exhibited good anthelmintic activity. The study revealed the necessity of synthesizing many more compounds with other substituents at position-4 of the benzene ring located at position-4 of pyrimidine. PMID:27413345

  18. Interstellar PAH Analogs in the Laboratory: Comparison with Astronomical Data

    NASA Technical Reports Server (NTRS)

    Salama, Farid

    2005-01-01

    Polycyclic Aromatic Hydrocarbons (PAHs) are an important and ubiquitous component of carbon-bearing materials in space. PAHs are the best-known candidates to account for the IR emission bands (UIR bands) and PAH spectral features are now being used as new probes of the ISM. PAHs are also thought to be among the carriers of the diffuse interstellar absorption bands (DIBs). In the model dealing with the interstellar spectral features, PAHs are present as a mixture of radicals, ions and neutral species. 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 for laboratory astrophysics is to reproduce (in a realistic way) the physical conditions that exist in the emission and/or absorption interstellar zones. An extensive laboratory program has been developed at NASA Ames to assess the physical and chemical properties of PAHs in such environments and to describe how they influence the radiation and energy balance in space and the interstellar chemistry. In particular, laboratory experiments provide measurements of the spectral characteristics of interstellar PAH analogs from the ultraviolet and visible range to the infrared range for comparison with astronomical data. This paper will focus on the recent progress made in the laboratory to measure the direct absorption spectra of neutral and ionized PAHs in the near-UV and visible range. Intrinsic band profiles and band positions of cold gas-phase PAHs can now be measured with high-sensitivity spectroscopy and directly compared to the astronomical data. Preliminary conclusions from the comparison of the laboratory data with astronomical observations will also be presented.

  19. Cloud deposition of PAHs at Mount Lushan in southern China.

    PubMed

    Wang, Ruixia; Wang, Yan; Li, Hongli; Yang, Minmin; Sun, Lei; Wang, Tao; Wang, Wenxing

    2015-09-01

    Cloud water samples were collected from Mount Lushan, a high alpine area of southern China, and analyzed using GC-MS to investigate the concentration levels, seasonal variations, particle-dissolved phase partitioning, ecological risk of PAHs and its relationship to the atmosphere and rainwater. The average concentration of total (dissolved+particle) PAHs in cloud water was 819.90 ng/L, which ranged from 2.30 ng/L for DbA to 295.38 ng/L for PhA. PhA (33.11%) contributed the most individual PAHs, followed by Flu (28.24%). Distinct seasonal variations in the total PAHs measured in this research had a higher concentration during the spring and a lower concentration during the summer. When cloud events occurred, the concentration of the atmospheric PAHs of the two phases decreased. The contribution from the gaseous phase of total PAHs in the air to the dissolved phase in cloud water was up to 60.43%, but the particulate phase in the air only contributed 39.57% to the total scavenging. The contribution of total PAHs from the atmosphere to clouds is higher in the gaseous phase than in the particulate phase. A comparative study of the concentrations of cloud water and the closest rain water revealed that the PAH concentration in rainwater was 1.80 times less than that of cloud water and that the dominant individual compounds in cloud water and rainwater were PhA and Flu. A total of 81.27% of the PAHs in cloud samples and 72.21% of the PAHs in rain samples remained in the dissolved phase. Ecological risk assessment indicated that PAHs in cloud water in spring and summer caused a certain degree of ecosystem risk and the mean ecosystem risk in spring was higher than that in summer. PMID:25967478

  20. 45 CFR 4.6 - Materials related to petitions under the National Vaccine Injury Compensation Program.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... Vaccine Injury Compensation Program. 4.6 Section 4.6 Public Welfare Department of Health and Human... Vaccine Injury Compensation Program. Notwithstanding the provisions of §§ 4.1, 4.2, and 4.3, service of..., shall be served upon the Director, Division of Vaccine Injury Compensation, Office of Special...

  1. 45 CFR 4.6 - Materials related to petitions under the National Vaccine Injury Compensation Program.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... Vaccine Injury Compensation Program. 4.6 Section 4.6 Public Welfare DEPARTMENT OF HEALTH AND HUMAN... Vaccine Injury Compensation Program. Notwithstanding the provisions of §§ 4.1, 4.2, and 4.3, service of..., shall be served upon the Director, Division of Vaccine Injury Compensation, Office of Special...

  2. 45 CFR 4.6 - Materials related to petitions under the National Vaccine Injury Compensation Program.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... Vaccine Injury Compensation Program. 4.6 Section 4.6 Public Welfare DEPARTMENT OF HEALTH AND HUMAN... Vaccine Injury Compensation Program. Notwithstanding the provisions of §§ 4.1, 4.2, and 4.3, service of..., shall be served upon the Director, Division of Vaccine Injury Compensation, Office of Special...

  3. 45 CFR 4.6 - Materials related to petitions under the National Vaccine Injury Compensation Program.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... Vaccine Injury Compensation Program. 4.6 Section 4.6 Public Welfare DEPARTMENT OF HEALTH AND HUMAN... Vaccine Injury Compensation Program. Notwithstanding the provisions of §§ 4.1, 4.2, and 4.3, service of..., shall be served upon the Director, Division of Vaccine Injury Compensation, Office of Special...

  4. 45 CFR 4.6 - Materials related to petitions under the National Vaccine Injury Compensation Program.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... Vaccine Injury Compensation Program. 4.6 Section 4.6 Public Welfare DEPARTMENT OF HEALTH AND HUMAN... Vaccine Injury Compensation Program. Notwithstanding the provisions of §§ 4.1, 4.2, and 4.3, service of..., shall be served upon the Director, Division of Vaccine Injury Compensation, Office of Special...

  5. 43 CFR 2650.4-6 - National wildlife refuge system lands.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 43 Public Lands: Interior 2 2011-10-01 2011-10-01 false National wildlife refuge system lands. 2650.4-6 Section 2650.4-6 Public Lands: Interior Regulations Relating to Public Lands (Continued) BUREAU OF LAND MANAGEMENT, DEPARTMENT OF THE INTERIOR LAND RESOURCE MANAGEMENT (2000) ALASKA NATIVE SELECTIONS Alaska Native Selections: Generally §...

  6. 16S rDNA-based probes for two polycyclic aromatic hydrocarbon (PAH)-degrading soil Mycobacteria

    SciTech Connect

    Govindaswami, M.; Feldhake, D.J.; Loper, J.C.

    1994-12-31

    PAHs are a class of widespread pollutants, some of which have been shown to be genotoxic, hence the fate of these compounds in the environment is of considerable interest. Research on the biodegradation of 4 and 5 ring PAHs has been limited by the general lack of microbial isolates or consortia which can completely degrade these toxicants. Heitkamp and Cerniglia have described an oxidative soil Mycobacterium-strain PYR-1 that metabolizes pyrene and fluoranthene more rapidly than the 2 and 3 ring naphthalene and phenanthrene; although some metabolites of benzo-(a)-pyrene (BaP) were detected, no mineralization of BaP was observed. In 1991 Grosser et al. reported the isolation of a Mycobacterium sp. which mineralizes pyrene and also causing some mineralization of BaP. Their study describes a comparative analysis of these two strains, which show very similar colony morphology, growth rate and yellow-orange pigmentation. Genetic differences were shown by DNA amplification fingerprinting (DAF) using two arbitrary GC-rich octanucleotide primers, and by sequence comparison of PCR amplified 16S rDNA, although both strains show similarity closest to that of the genus Mycobacteria. These 16S rDNA sequences are in use for the construction of strain-specific DNA probes to monitor the presence, survival and growth of these isolates in PAH-contaminated soils in studies of biodegradation.

  7. Are Urinary PAHs Biomarkers of Controlled Exposure to Diesel Exhaust?

    EPA Science Inventory

    Urinary polycyclic aromatic hydrocarbons (PAHs) were evaluated as possible biomarkers of exposure to diesel exhaust (DE) in two controlled-chamber studies. We report levels of 14 PAHs from 28 subjects in urine that were collected before, immediately after and the morning after ex...

  8. Solubilization, solution equilibria, and biodegradation of PAH's under thermophilic conditions.

    PubMed

    Viamajala, Sridhar; Peyton, Brent M; Richards, Lee A; Petersen, James N

    2007-01-01

    Biodegradation rates of PAHs are typically low at mesophilic conditions and it is believed that the kinetics of degradation is controlled by PAH solubility and mass transfer rates. Solubility tests were performed on phenanthrene, fluorene and fluoranthene at 20 degrees C, 40 degrees C and 60 degrees C and, as expected, a significant increase in the equilibrium solubility concentration and of the rate of dissolution of these polycyclic aromatic hydrocarbons (PAHs) was observed with increasing temperature. A first-order model was used to describe the PAH dissolution kinetics and the thermodynamic property changes associated with the dissolution process (enthalpy, entropy and Gibb's free energy of solution) were evaluated. Further, other relevant thermodynamic properties for these PAHs, including the activity coefficients at infinite dilution, Henry's law constants and octanol-water partition coefficients, were calculated in the temperature range 20-60 degrees C. In parallel with the dissolution studies, three thermophilic Geobacilli were isolated from compost that grew on phenanthrene at 60 degrees C and degraded the PAH more rapidly than other reported mesophiles. Our results show that while solubilization rates of PAHs are significantly enhanced at elevated temperatures, the biodegradation of PAHs under thermophilic conditions is likely mass transfer limited due to enhanced degradation rates. PMID:16934313

  9. The effects of PAH contamination on soil invertebrate communities

    SciTech Connect

    Snow-Ashbrook, J.L.; Erstfeld, K.M.

    1995-12-31

    Soils were collected from an abandoned industrial site to study the effects of historic polycyclic aromatic hydrocarbons (PAHs) on soil invertebrate communities. Nematode abundance and diversity, microarthropod abundance (orders Collembola and Acarina) and earthworm growth were evaluated. Physical and chemical characteristics of soils may affect both invertebrate community structure and the mobility/bioavailability of pollutants in soils. Soil characteristics were measured and included with PAH data in multiple regression analyses to identify factors which influences the responses observed in the soil invertebrate community. Positive associations were observed between eight invertebrate community endpoints and soil PAH content. For all of these endpoints but one, a higher degree of variability was explained when both PAH content and soil characteristics were considered. It is theorized that the positive response to soil PAH content may be the result of an increased abundance of PAH-degrading soil microbes. Increased microbial abundance could stimulate invertebrate communities by providing a direct food source or increasing the abundance of microbially-produced nutrients. These results suggest that both PAH content and soil characteristics significantly influenced the soil invertebrate community. It is not clear whether these factors influenced the invertebrate community independently, or whether differences in soil characteristics affected the community response by influencing the mobility or bioavailability of PAHs.

  10. PAH and OPAH Flux during the Deepwater Horizon Incident.

    PubMed

    Tidwell, Lane G; Allan, Sarah E; O'Connell, Steven G; Hobbie, Kevin A; Smith, Brian W; Anderson, Kim A

    2016-07-19

    Passive sampling devices were used to measure air vapor and water dissolved phase concentrations of 33 polycyclic aromatic hydrocarbons (PAHs) and 22 oxygenated PAHs (OPAHs) at four Gulf of Mexico coastal sites prior to, during and after shoreline oiling from the Deepwater Horizon oil spill (DWH). Measurements were taken at each site over a 13 month period, and flux across the water-air boundary was determined. This is the first report of vapor phase and diffusive flux of both PAHs and OPAHs during the DWH. Vapor phase sum PAH and OPAH concentrations ranged between 6.6 and 210 ng/m(3) and 0.02 and 34 ng/m(3) respectively. PAH and OPAH concentrations in air exhibited different spatial and temporal trends than in water, and air-water flux of 13 individual PAHs was shown to be at least partially influenced by the DWH incident. The largest PAH volatilizations occurred at the sites in Alabama and Mississippi at nominal rates of 56 000 and 42 000 ng/m(2) day(-1) in the summer. Naphthalene was the PAH with the highest observed volatilization rate of 52 000 ng/m(2) day(-1) in June 2010. This work represents additional evidence of the DWH incident contributing to air contamination, and provides one of the first quantitative air-water chemical flux determinations with passive sampling technology. PMID:27391856

  11. Solubilization, Solution Equilibria, and Biodegradation of PAH's under Thermophilic Conditions

    SciTech Connect

    Viamajala, S.; Peyton, B. M.; Richards, L. A.; Petersen, J. N.

    2007-01-01

    Biodegradation rates of PAHs are typically low at mesophilic conditions and it is believed that the kinetics of degradation is controlled by PAH solubility and mass transfer rates. Solubility tests were performed on phenanthrene, fluorene and fluoranthene at 20 C, 40 C and 60 C and, as expected, a significant increase in the equilibrium solubility concentration and of the rate of dissolution of these polycyclic aromatic hydrocarbons (PAHs) was observed with increasing temperature. A first-order model was used to describe the PAH dissolution kinetics and the thermodynamic property changes associated with the dissolution process (enthalpy, entropy and Gibb's free energy of solution) were evaluated. Further, other relevant thermodynamic properties for these PAHs, including the activity coefficients at infinite dilution, Henry's law constants and octanol-water partition coefficients, were calculated in the temperature range 20-60 C. In parallel with the dissolution studies, three thermophilic Geobacilli were isolated from compost that grew on phenanthrene at 60 C and degraded the PAH more rapidly than other reported mesophiles. Our results show that while solubilization rates of PAHs are significantly enhanced at elevated temperatures, the biodegradation of PAHs under thermophilic conditions is likely mass transfer limited due to enhanced degradation rates.

  12. PAH Measurements in Air in the Athabasca Oil Sands Region.

    PubMed

    Hsu, Yu-Mei; Harner, Tom; Li, Henrik; Fellin, Phil

    2015-05-01

    Polycyclic aromatic hydrocarbon (PAH) measurements were conducted by Wood Buffalo Environmental Association (WBEA) at four community ambient Air quality Monitoring Stations (AMS) in the Athabasca Oil Sands Region (AOSR) in Northeastern Alberta, Canada. The 2012 and 2013 mean concentrations of a subset of the 22 PAH species were 9.5, 8.4, 8.8, and 32 ng m(-3) at AMS 1 (Fort McKay), AMS 6 (residential Fort McMurray), AMS 7 (downtown Fort McMurray), and AMS 14 (Anzac), respectively. The average PAH concentrations in Fort McKay and Fort McMurray were in the range of rural and semirural areas, but peak values reflect an industrial emission influence. At these stations, PAHs were generally associated with NO, NO2, PM2.5, and SO2, indicating the emissions were from the combustion sources such as industrial stacks, vehicles, residential heating, and forest fires, whereas the PAH concentrations at AMS 14 (∼35 km south of Fort McMurray) were more characteristic of urban areas with a unique pattern: eight of the lower molecular weight PAHs exhibited strong seasonality with higher levels during the warmer months. Enthalpies calculated from Clausius-Clapeyron plots for these eight PAHs suggest that atmospheric emissions were dominated by temperature-dependent processes such as volatilization at warm temperatures. These findings point to the potential importance of localized water-air and/or surface-air transfer on observed PAH concentrations in air. PMID:25844542

  13. Dissipation of PAHs in saturated, dredged sediments: a field trial.

    PubMed

    Smith, K E; Schwab, A P; Banks, M K

    2008-08-01

    Sediments dredged from navigable rivers often contain elevated concentrations of recalcitrant, potentially toxic organic compounds such as polychlorinated biphenyls (PCBs) and polyaromatic hydrocarbons (PAHs). The presence of these compounds often requires that the sediments be stored in fully contained disposal facilities. A 3-year field study was conducted at the Jones Island disposal facility in Milwaukee, Wisconsin, to compare bioremediation of PAHs in contaminated dredged sediments in the absence of plants to phytoremediation with Salix nigra (black willow) (SX61), Spartina pectinata (prairie cord grass), Carex aquatalis (lake sedge), Lolium multiflorum (annual rye), and Scirpus fluviatilis (bulrush). Nine PAHs were detected initially in the sediments. Over the 3-year experiment, acenaphthene dissipation ranged from 94% to 100%, whereas anthracene, benzo[a]pyrene and indo[1,2,3-cd]pyrene generally had modest decreases in concentration (0-30% decrease). The remaining five PAHs ranged in degree of disappearance from 23% to 82%. Planted treatments did not enhance PAH dissipation relative to those without plants, but treatments with high biomass yield and high transpiration plant species had significantly less removal of PAHs than unplanted controls. Significant, negative correlations between nitrogen removal and decreases in PAH concentration suggest that competition for nutrients between plants and microorganisms may have impeded the microbial degradation of PAHs in the rhizosphere of the more rapidly growing plant species. PMID:18547603

  14. [Comparison of polycyclic aromatic hydrocarbons (PAHS) contents in bakery products].

    PubMed

    Ciemniak, Artur; Witczak, Agata

    2010-01-01

    Polycyclic aromatic hydrocarbons are a group of well-known chemical carcinogens with a wide distribution in the environment and formed by the incomplete combustion of organic substances. PAHs have attracted most attention because of their carcinogenic potential. PAHs have been found as contaminants in different food categories such as dairy products, smoked and barbecued meat, vegetables, fruits, oils, coffee, tea, and cereals. Processing of food at high temperatures increases the amount of PAHs in the food Diet is the major source of human exposure to PAHs. The major dietary source of PAH are oils and fats, cereals products and vegetables. The aims of this study were to determine the content levels of 23 PAHs in various sorts of bread. The analytical procedure was based Soxhlet extraction with n--hexane and cleaned up in aflorisil cartridge. Chromatographic separation was performed using gas chromatography (HP 6890) coupled to mass spectrometry (HP 5973). The total concentration of PAHs was low end varied between 2.61 microg/kg to 43.4 microg/kg. Furthermore, the results revealed differences in concentrations of PAHs between rind and bread-crumb. PMID:20839459

  15. PAH bombardment by energetic particles: models and astrophysical implications

    NASA Astrophysics Data System (ADS)

    Micelotta, E.; Jones, A.; Tielens, A.

    2011-05-01

    Polycyclic Aromatic Hydrocarbons (PAHs) are an important and ubiquitous component of the Interstellar Medium (ISM) of galaxies. Interstellar PAHs are apparently able to withstand the rigors of the harsh environment of the ISM for some some 100 million years and thus are resilient against processing by UV and X-ray photons and supernova shock waves. PAHs in space are mainly studied through their characteristic emission bands, due to infrared fluorescence following the absorption of UV photons. This is the reason why the photophysics of PAHs in space has been extensively investigated. On the other hand, PAHs are also strongly affected by collisional processes, i.e. bombardment by high-velocity ions and electrons, arising from interstellar shocks, hot gas and cosmic rays. However, very little was known about the physics of the interaction between PAHs and high energy particles, especially in terms of PAH damage and destruction. This lack of information had made the interpretation of PAH observations difficult in regions subjected to such processes. Our research aims to fill this key gap in our understanding of the physics behind collisional processing of PAHs and to clarify how this affects the PAH evolution in the astrophysical context. We first describe the models we have developed, that take into account the molecular nature of the target PAH and allow for the first time a quantitative description of the collisional processing of PAH molecules by ions and electrons with energies between 10 eV and 10 keV (in shocks and hot gas) and between 5 MeV and 10 GeV (in cosmic rays). Specific models were needed because PAHs are molecules and not small solid fragments, thus the classical approach from solid state physics cannot be applied. We then show the applications of our models to observations, estimating the lifetime of PAHs against collisional processing in specific objects. We discuss the astrophysical implications of our findings on the considered sample, which

  16. Enhanced bioremediation of PAH contaminated soils from coal processing sites

    SciTech Connect

    Joshi, M.M.; Lee, S.

    1995-12-31

    The polycyclic aromatic hydrocarbons (PAH) are a potential hazard to health due to their carcinogenic, mutagenic nature and acute toxicity and there is an imminent need for remediation of PAH contaminated soils abounding the several coke oven and town gas sites. Aerobic biological degradation of PAHs is an innovative technology and has shown high decontamination efficiencies, complete mineralization of contaminants, and is environmentally safe. The present study investigates the remediation of PAH contaminated soils achieved using Acinetobacter species and fungal strain Phanerochaete Chrysosporium. The soil used for the experiments was an industrially contaminated soil obtained from Alberta Research Council (ARC) primary cleanup facility, Alberta, Canada. Soil characterization was done using High Performance Liquid Chromatography (HPLC) to qualitatively and quantitatively determine the contaminants in the soil. Artificially contaminated soil was also used for some experiments. All the experiments were conducted under completely mixed conditions with suitable oxygen and nutrient amendments. The removal efficiency obtained for various PAHs using the two microorganisms was compared.

  17. PAH Clusters and the Interstellar Infrared Emission Bands

    NASA Astrophysics Data System (ADS)

    Ricca, Alessandra; Roser, Joseph

    2016-06-01

    Polycyclic aromatic hydrocarbons (or PAHs) are the leading candidate for the emitters of the interstellar aromatic infrared emission bands. Some aspects of these emission bands indicate a contribution from PAH clusters. To better assess this contribution, we measured infrared absorption spectra of a series of homogeneous and heterogeneous PAH clusters using matrix isolation spectroscopy in solid argon and we performed theoretical calculations. The spectral shifts observed in the absorption spectra as a function of the PAH concentration can be related to preferred cluster structures forming in the argon matrix. Based upon our results, we predict that the large PAHs present in the interstellar medium are likely to have clusters with redshifted absorption bands in the C–H out-of-plane bending region. These clusters could contribute to a well-known red-shading observed in the profile of the interstellar 11.2 micron emission band.

  18. Comparative Developmental Toxicity of Environmentally Relevant Oxygenated PAHs

    SciTech Connect

    Knecht, Andrea; Goodale, Britton; Truong, Lisa; Simonich, Michael; Swanson, Annika; Matzke, Melissa M.; Anderson, Kim A.; Waters, Katrina M.; Tanguay, Robert

    2013-09-01

    Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous pollutants in urban air, dust and in the soil of most industrial coal gassification, coal burning, coke production and wood preservation sites (Howsam and Jones 1998). It is widely recognized that PAHs pose risks to human health,having been associated with increased risks of systemic inflammation (Delfino et al. 2010), cardiopulmonary mortality (Lee et al. 2011; Lewtas 2007) and lung cancer mortality (Grant 2009; Hoshuyama et al. 2006). The potential risks may be especially acute for the developing fetus and infant where PAH exposures have been linked to low birth weight, intrauterine growth retardation, in-utero mortality and lower intelligence (Dejmek et al. 1999; Dejmek et al. 2000; Perera et al. 1999; Perera et al. 2009; Perera et al. 2006; Perera et al. 1998; Wu et al. 2010). Despite the more than two decades of intensive study devoted to parent PAHs, they are only part of the hazard spectrum from PAH contamination.

  19. Polynuclear aromatic hydrocarbons (PAHs) in fish from the Arabian Gulf

    SciTech Connect

    DouAbdul, A.A.Z.; Abaychi, J.K.; Al-Edanee, T.E.; Ghani, A.A.; Al-Saad, H.T.

    1987-03-01

    Emphasis has been placed upon the identification and qualification of compounds with potential adverse health effects on humans. Prominent among this group are polynuclear aromatic hydrocarbons (PAHs), several of which are known or suspected carcinogens. PAHs enter the marine environment from a variety of sources including petroleum pollution, industrial and domestic effluents, atmospheric particles, and biosynthesis by plants and microorganisms. Although one-third of the world's oil is produced around the Arabian Gulf, no detailed analysis have been conducted to determine PAHs in this region. Nevertheless, numerous investigations have shown the ability of marine organisms including fish to accumulation PAHs from solution or dispersion in seawater. When fish are harvested, a human health hazard may result. In the present communication, high performance liquid chromatography (HPLC) was used to identify and measure sixteen PAHs priority pollutants issued by US Environmental Protection Agency (EPA) in fourteen species of commercially significant fish from the NW Arabian Gulf.

  20. Structural stability, NH 2 inversion and vibrational assignments of 2,4,6-trichloroaniline and 2,3,5,6-tetrachloroaniline

    NASA Astrophysics Data System (ADS)

    Badawi, Hassan M.; Förner, Wolfgang; Al-Saadi, Abdulaziz A.

    2009-12-01

    The structural stability of aniline, 2,4,6-trichloroaniline and 2,3,5,6-tetrachloroaniline was investigated by DFT-B3LYP and ab initio MP2 and MP4(SDQ) calculations with the 6-311G∗∗ basis set. From the calculations the three molecules were predicted to exist predominantly in a symmetric near-planar structure. The NH 2 inversion barrier was estimated from the MP2/6-311G∗∗ level of theory to be about 9.6 kJ/mol for aniline, 5.9 kJ/mol for the trichloro and 4.6 kJ/mol for the tetrachloro derivatives. The line intensities of the ring breathing and the C sbnd Cl stretching modes were shown to have a great dependence on the number of chlorine atoms on the benzene ring. The relative change in Raman line intensity of the C sbnd Cl stretching mode was explained on the basis of the inductive effect of the chlorine atoms on the benzene ring. The vibrational frequencies were computed at the DFT-B3LYP level and the infrared and Raman spectra for each molecule were calculated. Complete vibrational assignments were made on the basis of normal coordinate analyses and potential energy distributions for the two chloroanilines.

  1. Metabolic Reprogramming of Pancreatic Cancer Mediated by CDK4/6 Inhibition Elicits Unique Vulnerabilities.

    PubMed

    Franco, Jorge; Balaji, Uthra; Freinkman, Elizaveta; Witkiewicz, Agnieszka K; Knudsen, Erik S

    2016-02-01

    Due to loss of p16ink4a in pancreatic ductal adenocarcinoma (PDA), pharmacological suppression of CDK4/6 could represent a potent target for treatment. In PDA models, CDK4/6 inhibition had a variable effect on cell cycle but yielded accumulation of ATP and mitochondria. Pharmacological CDK4/6 inhibitors induce cyclin D1 protein levels; however, RB activation was required and sufficient for mitochondrial accumulation. CDK4/6 inhibition stimulated glycolytic and oxidative metabolism and was associated with an increase in mTORC1 activity. MTOR and MEK inhibitors potently cooperate with CDK4/6 inhibition in eliciting cell-cycle exit. However, MTOR inhibition fully suppressed metabolism and yielded apoptosis and suppression of tumor growth in xenograft models. The metabolic state mediated by CDK4/6 inhibition increases mitochondrial number and reactive oxygen species (ROS). Concordantly, the suppression of ROS scavenging or BCL2 antagonists cooperated with CDK4/6 inhibition. Together, these data define the impact of therapeutics on PDA metabolism and provide strategies for converting cytostatic response to tumor cell killing. PMID:26804906

  2. ON THE VIABILITY OF THE PAH MODEL AS AN EXPLANATION OF THE UNIDENTIFIED INFRARED EMISSION FEATURES

    SciTech Connect

    Zhang, Yong; Kwok, Sun E-mail: sunkwok@hku.hk

    2015-01-01

    Polycyclic aromatic hydrocarbon (PAH) molecules are widely considered the preferred candidate for the carrier of the unidentified infrared emission bands observed in the interstellar medium and circumstellar envelopes. In this paper, we report the results of fitting a variety of non-PAH spectra (silicates, hydrogenated amorphous carbon, coal, and even artificial spectra) using the theoretical infrared spectra of PAHs from the NASA Ames PAH IR Spectroscopic Database. We show that these non-PAH spectra can be well fitted by PAH mixtures. This suggests that a general match between astronomical spectra and those of PAH mixtures does not necessarily provide definitive support for the PAH hypothesis.

  3. Penta- and 2,4,6-tri-chlorophenol biodegradation during municipal solid waste anaerobic digestion.

    PubMed

    Limam, Intissar; Limam, Rim Driss; Mezni, Mohamed; Guenne, Angéline; Madigou, Céline; Driss, Mohamed Ridha; Bouchez, Théodore; Mazeas, Laurent

    2016-08-01

    In this study isotopic tracing using (13)C labelled pentachlorophenol (PCP) and 2,4,6-trichlorophenol (2,4,6-TCP) is proposed as a tool to distinguish the loss of PCP and 2,4,6-TCP due to biodegradation from other physical processes. This isotopic approach was applied to accurately assess in situ PCP and 2,4,6-TCP degradation under methanogenic conditions in several microcosms made up of household waste. These microcosms were incubated in anaerobic conditions at 35°C (mesophilic) and 55°C (thermophilic) without agitation. The volume of biogas produced (CH4 and CO2), was followed for a period of 130 days. At this stage of stable methanogenesis, (13)C6-PCP and (13)C6-2,4,6-TCP were introduced anaerobically in microcosms and its monitoring at mesophilic and thermophilic conditions was performed in parallel by gas chromatography mass spectrometry (GC-MS) and gas chromatography isotope-ratio mass spectrometry (GC-IRMS). This study proved the almost total dechlorination of bioavailable PCP and 2,4,6-TCP into 4-CP at 35°C. Nevertheless, high rate adsorption in particular materials of the two compounds was observed. Furthermore, Carbon-13 Nuclear Magnetic Resonance ((13)C-NMR) Spectroscopy analysis of (13)C labelled 2,4,6-TCP mesophilic incubations showed the partial mineralization of 4-CP at 35°C to acetate and then to HCO(3-). Consequently, NMR results confirm the biogas isotopic results indicating the mineralization of (13)C labelled 2,4,6-TCP into (13)C (CH4 and CO2). Concerning (13)C labelled PCP mesophilic incubations, the isotopic composition of the biogas still natural until the day 262. In contrast, no dechlorination was observed at 55°C. Thus PCP and 2,4,6-TCP were persistent in thermophilic conditions. PMID:27151678

  4. Interstellar PAH in the Laboratory and in Space. What have we Learned from the New Generation of Laboratory and Observational Studies?

    NASA Technical Reports Server (NTRS)

    Salama, Farid

    2005-01-01

    an isolated environment at low temperature (of the order of 100 K). The spectra of neutral and ionized PAHs are measured using the high sensitivity methods of cavity ring down spectroscopy (CRDS). These experiments provide unique information on the spectra of free, cold large carbon molecules and ions in the gas phase. Intrinsic band profiles and band positions of cold gas-phase PAHs can now be measured with high-sensitivity spectroscopy and directly compared to the astronomical data. The electronic bands measured for ionized PAH are found to be intrinsically broad (about 20 cm(sup -1)) while the bands associated with the neutral precursors are narrower (of the order of 2 - 10 cm(sup -1)). The laboratory data are discussed and compared with recent astronomical spectra of large and narrow DIBs and with the spectra of circumstellar environments of selected carbon stars and the implications for the interstellar PAH population are derived. Preliminary results also show that carbon nanoparticles are formed during the short residence time of the precursors in the plasma.

  5. Coal-Tar-Sealcoated Parking Lots: "Hot spots" of PAHs and N-heterocycles to Urban Streams and Lakes Result in "Hot Moments" of Toxicity

    NASA Astrophysics Data System (ADS)

    Mahler, B. J.; Van Metre, P. C.; Ingersoll, C.; Kunz, J. L.

    2014-12-01

    Coal-tar (CT) sealcoat, a potent source of polycyclic aromatic hydrocarbons (PAHs) and N-heterocycles, is applied to asphalt pavement of parking lots and driveways in many parts of the U.S. and Canada every 1 to 5 years. We measured the chemistry and toxicity of unfiltered runoff resulting from rain events simulated from 5 hours to 111 days after application of CT or asphalt (AS) sealcoat. PAHs and N-heterocycles were measured by GC/EIMS. Toxicity tests were done with Ceriodaphnia dubia and Pimephales promelas exposed 48 hours to undiluted and diluted (1 part runoff 9 parts control water) runoff under ambient lighting. Organisms were then transferred to fresh control water and subjected to a 4-hour pulse of ultraviolet radiation (UVR). Concentrations of 2- and 3-ringed PAHs and N-heterocycles in CT runoff, initially high (sum of 6 PAHs, 220 μg/L; sum of 7 N-heterocycles, 904 μg/L), decreased rapidly, whereas concentrations of 4-, 5- and 6-ringed PAHs more than doubled by 7 days after application (sum of 9 PAHs, 378 μg/L) and remained elevated 111 days after application (sum of 9 PAHs, 283 μg/L). Concentrations of PAHs and N-heterocycles in AS sealcoated runoff followed a similar pattern, but were ~10 times lower than those in CT runoff; concentrations in a sample of runoff from unsealed asphalt pavement were near or less than the detection limit. Organisms exposed to samples of undiluted CT-runoff collected during the 36 days following CT sealcoat application (no UVR exposure) experienced 100% mortality. Mortality (as much as 100%) of organisms exposed to the 10% dilution of CT runoff or to undiluted AS runoff occurred only with UVR; mortality of organisms exposed to the 10% solution of AS runoff and UVR was minimal. Results demonstrate that freshly CT-sealed parking lots and driveways are "hot spots" of PAH and N-heterocycle contamination and that prolonged "hot moments" of toxicity follow CT sealcoat application.

  6. Polycyclic aromatic hydrocarbon (PAH) and oxygenated PAH (OPAH) air-water exchange during the deepwater horizon oil spill.

    PubMed

    Tidwell, Lane G; Allan, Sarah E; O'Connell, Steven G; Hobbie, Kevin A; Smith, Brian W; Anderson, Kim A

    2015-01-01

    Passive sampling devices were used to measure air vapor and water dissolved phase concentrations of 33 polycyclic aromatic hydrocarbons (PAHs) and 22 oxygenated PAHs (OPAHs) at four Gulf of Mexico coastal sites prior to, during, and after shoreline oiling from the Deepwater Horizon oil spill (DWH). Measurements were taken at each site over a 13 month period, and flux across the water-air boundary was determined. This is the first report of vapor phase and flux of both PAHs and OPAHs during the DWH. Vapor phase sum PAH and OPAH concentrations ranged between 1 and 24 ng/m(3) and 0.3 and 27 ng/m(3), respectively. PAH and OPAH concentrations in air exhibited different spatial and temporal trends than in water, and air-water flux of 13 individual PAHs were strongly associated with the DWH incident. The largest PAH volatilizations occurred at the sites in Alabama and Mississippi in the summer, each nominally 10,000 ng/m(2)/day. Acenaphthene was the PAH with the highest observed volatilization rate of 6800 ng/m(2)/day in September 2010. This work represents additional evidence of the DWH incident contributing to air contamination, and provides one of the first quantitative air-water chemical flux determinations with passive sampling technology. PMID:25412353

  7. Polycyclic Aromatic Hydrocarbon (PAH) and Oxygenated PAH (OPAH) Air–Water Exchange during the Deepwater Horizon Oil Spill

    PubMed Central

    2015-01-01

    Passive sampling devices were used to measure air vapor and water dissolved phase concentrations of 33 polycyclic aromatic hydrocarbons (PAHs) and 22 oxygenated PAHs (OPAHs) at four Gulf of Mexico coastal sites prior to, during, and after shoreline oiling from the Deepwater Horizon oil spill (DWH). Measurements were taken at each site over a 13 month period, and flux across the water–air boundary was determined. This is the first report of vapor phase and flux of both PAHs and OPAHs during the DWH. Vapor phase sum PAH and OPAH concentrations ranged between 1 and 24 ng/m3 and 0.3 and 27 ng/m3, respectively. PAH and OPAH concentrations in air exhibited different spatial and temporal trends than in water, and air–water flux of 13 individual PAHs were strongly associated with the DWH incident. The largest PAH volatilizations occurred at the sites in Alabama and Mississippi in the summer, each nominally 10 000 ng/m2/day. Acenaphthene was the PAH with the highest observed volatilization rate of 6800 ng/m2/day in September 2010. This work represents additional evidence of the DWH incident contributing to air contamination, and provides one of the first quantitative air–water chemical flux determinations with passive sampling technology. PMID:25412353

  8. Modulation of the Effect of Prenatal PAH Exposure on PAH-DNA Adducts in Cord Blood by Plasma Antioxidants

    PubMed Central

    Kelvin, Elizabeth A.; Edwards, Susan; Jedrychowski, Wieslaw; Schleicher, Rosemary L.; Camann, David; Tang, Deliang; Perera, Frederica P.

    2011-01-01

    The fetus is more susceptible than the adult to the effects of certain carcinogens, such as polycyclic aromatic hydrocarbons (PAH). Nutritional factors, including antioxidants, have been shown to have a protective effect on carcinogen-DNA adducts and cancer risk in adults. We investigated whether the effect of prenatal airborne PAH exposure, measured by personal air monitoring during pregnancy, on the level of PAH-DNA adducts in a baby's cord blood is modified by the concentration of micronutrients in maternal and cord blood. The micronutrients examined were: retinol (vitamin A), α-tocopherol and γ-tocopherol (vitamin E), and carotenoids. With the use of multiple linear regression, we found a significant interaction between prenatal PAH exposure and cord blood concentration of α-tocopherol and carotenoids in predicting the concentration of PAH adducts in cord blood. The association between PAH exposure and PAH adducts was much stronger among those with low α-tocopherol (β = 0.15; P = 0.001) and among those with low carotenoids (β = 0.16; P < 0.001) compared with babies with high levels of these micronutrients (among those with high α-tocopherol: β = 0.05; P = 0.165; among those with high carotenoids: β = 0.06; P = 0.111). These results suggest a protective effect of micronutrients on the DNA damage and potential cancer risk associated with prenatal PAH exposure. PMID:19661084

  9. Asymmetric dipolar ring

    DOEpatents

    Prosandeev, Sergey A.; Ponomareva, Inna V.; Kornev, Igor A.; Bellaiche, Laurent M.

    2010-11-16

    A device having a dipolar ring surrounding an interior region that is disposed asymmetrically on the ring. The dipolar ring generates a toroidal moment switchable between at least two stable states by a homogeneous field applied to the dipolar ring in the plane of the ring. The ring may be made of ferroelectric or magnetic material. In the former case, the homogeneous field is an electric field and in the latter case, the homogeneous field is a magnetic field.

  10. On the common modulus attack into the LUC4,6 cryptosystem

    NASA Astrophysics Data System (ADS)

    Wong, Tze Jin; Said, Mohd Rushdan Md; Othman, Mohamed; Koo, Lee Feng

    2015-05-01

    The LUC4,6 cryptosystem is a system analogy with RSA cryptosystem and extended from LUC and LUC3 cryptosystems. The process of encryption and decryption are derived from the fourth order linear recurrence sequence and based on Lucas function. This paper reports an investigation into the common modulus attack on the LUC4,6 cryptosystem. In general, the common modulus attack will be succeeded if the sender sends the plaintext to two users used same RSA-modulus and both of encryption keys of them are relatively prime to each other. However, based on the characteristics of high order Lucas sequence, the LUC4,6 cryptosystem is unattackable

  11. 1-(Piperidin-1-yl)-3-(2,4,6-trimethyl-phen-yl)propan-2-ol.

    PubMed

    Maharramov, Abel M; Khalilov, Ali N; Gurbanov, Atash V; Allahverdiyev, Mirze A; Ng, Seik Weng

    2011-01-01

    The title compound, C(17)H(27)NO, features a bufferfly-shaped substituted 2-propanol having an aromatic ring on the 1-carbon and a piperidine ring on the 3-carbon. The piperidine ring adopts a chair conformation and its N atom shows a trigonal coordination. In the crystal, the hy-droxy group inter-acts with the N atom of an inversion-related mol-ecule, generating an O-H⋯N hydrogen-bonded dimer. PMID:21522478

  12. Mapping PAH sizes in NGC 7023 with SOFIA

    NASA Astrophysics Data System (ADS)

    Croiset, B. A.; Candian, A.; Berné, O.; Tielens, A. G. G. M.

    2016-05-01

    Context. NGC 7023 is a well-studied reflection nebula, which shows strong emission from polycyclic aromatic hydrocarbon (PAH) molecules in the form of aromatic infrared bands (AIBs). The spectral variations of the AIBs in this region are connected to the chemical evolution of the PAH molecules which, in turn, depends on the local physical conditions. Aims: Our goal is to map PAH sizes in NGC 7023 with respect to the location of the star. We focus on the north west (NW) photo-dissociation region (PDR) and the south PDR of NGC 7023 to understand the photochemical evolution of PAHs, using size as a proxy. Methods: We use the unique capabilities of the Stratospheric Observatory for Infrared Astronomy (SOFIA) to observe a 3.2' × 3.4' region of NGC 7023 at wavelengths that we observe with high spatial resolution (2.7'') at 3.3 and 11.2 μm. We compare the SOFIA images with existing images of the PAH emission at 8.0 μm (Spitzer), emission from evaporating very small grains (eVSG) extracted from Spitzer-IRS spectral cubes, the extended red emission (Hubble Space Telescope and Canadian French Hawaiian Telescope), and H2 (2.12 μm). We create maps of the 11.2/3.3 μm ratio to probe the morphology of the PAH size distribution and the 8.0/11.2 μm ratio to probe the PAH ionization. We make use of an emission model and of vibrational spectra from the NASA Ames PAH database to translate the 11.2/3.3 μm ratio to PAH sizes. Results: The 11.2/3.3 μm ratio map shows the smallest PAH concentrate on the PDR surface (H2 and extended red emission) in the NW and south PDR. We estimated that PAHs in the NW PDR bear, on average, a number of carbon atoms (Nc) of ~70 in the PDR cavity and ~50 at the PDR surface. In the entire nebula, the results reveal a factor of 2 variation in the size of the PAH. We relate these size variations to several models for the evolution of the PAH families when they traverse from the molecular cloud to the PDR. Conclusions: The high-resolution PAH size map

  13. Comparative developmental toxicity of environmentally relevant oxygenated PAHs

    SciTech Connect

    Knecht, Andrea L.; Goodale, Britton C.; Truong, Lisa; Simonich, Michael T.; Swanson, Annika J.; Matzke, Melissa M.; Anderson, Kim A.; Waters, Katrina M.; Tanguay, Robert L.

    2013-09-01

    Oxygenated polycyclic aromatic hydrocarbons (OPAHs) are byproducts of combustion and photo-oxidation of parent PAHs. OPAHs are widely present in the environment and pose an unknown hazard to human health. The developing zebrafish was used to evaluate a structurally diverse set of 38 OPAHs for malformation induction, gene expression changes and mitochondrial function. Zebrafish embryos were exposed from 6 to 120 h post fertilization (hpf) to a dilution series of 38 different OPAHs and evaluated for 22 developmental endpoints. AHR activation was determined via CYP1A immunohistochemistry. Phenanthrenequinone (9,10-PHEQ), 1,9-benz-10-anthrone (BEZO), xanthone (XAN), benz(a)anthracene-7,12-dione (7,12-B[a]AQ), and 9,10-anthraquinone (9,10-ANTQ) were evaluated for transcriptional responses at 48 hpf, prior to the onset of malformations. qRT-PCR was conducted for a number of oxidative stress genes, including the glutathione transferase(gst), glutathione peroxidase(gpx), and superoxide dismutase(sod) families. Bioenergetics was assayed to measure in vivo oxidative stress and mitochondrial function in 26 hpf embryos exposed to OPAHs. Hierarchical clustering of the structure-activity outcomes indicated that the most toxic of the OPAHs contained adjacent diones on 6-carbon moieties or terminal, para-diones on multi-ring structures. 5-carbon moieties with adjacent diones were among the least toxic OPAHs while the toxicity of multi-ring structures with more centralized para-diones varied considerably. 9,10-PHEQ, BEZO, 7,12-B[a]AQ, and XAN exposures increased expression of several oxidative stress related genes and decreased oxygen consumption rate (OCR), a measurement of mitochondrial respiration. Comprehensive in vivo characterization of 38 structurally diverse OPAHs indicated differential AHR dependency and a prominent role for oxidative stress in the toxicity mechanisms. - Highlights: • OPAHs are byproducts of combustion present in the environment. • OPAHs pose a largely

  14. Potential threat of heavy metals and PAHs in PM2.5 in different urban functional areas of Beijing

    NASA Astrophysics Data System (ADS)

    Gao, Yang; Guo, Xinyue; Ji, Hongbing; Li, Cai; Ding, Huaijian; Briki, Meryem; Tang, Lei; Zhang, Yan

    2016-09-01

    Beijing, as the capital of China, is one of the most populous cities in the world. With the fine particulate matter pollution being increasingly serious, daily exposure to hazardous ingredients caused more and more attention. Current research concerning risk evaluation in Beijing was relative less. In November, 2013, samples were collected in seven different functional areas of Beijing, so as to better understand the risk to human health caused by particle matter pollution in this region. PM2.5 pollution in rural and urban Beijing was relative high under haze-fog days in comparison with non haze-fog value. Zn and Ba showed the highest concentration levels among non-carcinogenic metals. The non-carcinogenic metal concentration at all the sites ranged in the same order: Ce, Pb, Cu, V and Sb. Higher ring PAHs (with four to six rings) were the dominant species and constituted more than 90% of the Σ14PAHs. Pb (4.34 × 10- 4 for men, 3.73 × 10- 4 for women) presented the maximum risk level for non-carcinogenic heavy metals in the whole study area. While, risk levels of Cr at residential areas, schools, Olympic Park and rural countryside exceeded the limit for adults. In haze-fog days, the carcinogenic PAH risk level in each functional area ranged in the order: rural countryside > inner suburban district > Olympic Park > city central > schools > ecological reserve > residential areas. To some extent, benzo(a)pyrene may had a potential risk to adults, and other carcinogenic PAHs were all under average risk acceptance.

  15. Optimization and comparison of miniaturized extraction techniques for PAHs from crude oil exposed Atlantic cod and haddock eggs.

    PubMed

    Sørensen, Lisbet; Silva, Marta S; Booth, Andy M; Meier, Sonnich

    2016-02-01

    Two miniaturized extraction methods for a wide range of 2-6 ring polycyclic aromatic hydrocarbons (PAHs) and their alkylated homologues in small lipid-rich biota samples (≤100 mg) have been developed. Both methods utilize liquid extraction (LE) prior to a clean-up step using either normal phase solid phase extraction (SPE) or mixed-phase dispersive SPE (dSPE). Optimization of the methods was achieved by comparing the type and amount of sorbents, drying agents, and solvents used. In order to improve the limits of detection (LOD) of target PAHs under high sensitivity gas chromatography-tandem mass spectrometry analysis, specific emphasis was given to minimizing lipid co-extraction. The optimized LE-SPE method comprised extraction with dichloromethane/n-hexane (1:1, v/v) and clean-up by silica SPE, whereas the optimized LE-dSPE method comprised extraction with acetonitrile and clean-up with PSA and C18 sorbents. The methods were validated and directly compared through the analysis of Atlantic cod (Gadus morhua) and haddock (Melanogrammus aeglefinus) eggs exposed to oil. The LE-SPE method resulted in lower levels of co-extracted lipids (14.1 ± 1.7 ng/μL) than the LE-dSPE method (60 ± 14 ng/μL). Achieved PAH LODs for the LE-SPE method were typically an order of magnitude lower (<5 ng/g) than for the LE-dSPE method (<125 ng/g). The LE-SPE method offers the possibility for PAH analysis of small samples of fish eggs (~100 mg) exposed to small quantities of crude oil (~1-10 μg/L total PAHs). PMID:26677025

  16. PAH related effects on fish in sedimentation ponds for road runoff and potential transfer of PAHs from sediment to biota.

    PubMed

    Grung, Merete; Petersen, Karina; Fjeld, Eirik; Allan, Ian; Christensen, Jan H; Malmqvist, Linus M V; Meland, Sondre; Ranneklev, Sissel

    2016-10-01

    Road runoff is an important source of pollution to the aquatic environment, and sedimentation ponds have been installed to mitigate effects on the aquatic environment. The purpose of this study was to investigate if a) fish from sedimentation ponds were affected by road pollution and; b) the transfer of PAHs from road runoff material to aquatic organisms was substantial. Minnow from a sedimentation pond (Skullerud) near Oslo (Norway) had higher levels of CYP1A enzyme and DNA stand breaks than minnow from the nearby river, but high concentrations of PAH-metabolites in bile revealed that both populations were highly exposed. Principal component analysis revealed that CYP1A and age of fish were correlated, while levels of PAH-metabolites were not correlated to CYP1A or DNA damage. Minnow from a lake un-affected by traffic had much lower levels of PAH-metabolites than the exposed fish, and also an improved condition. The latter results indicate that fish health was affected by road runoff. A closer investigation of PAH levels of the ecosystems of two sedimentation ponds (Skullerud and Vassum) and nearby environments were conducted. The concentration of the 16 EPA PAHs in sediments of the sedimentation ponds were high (1900-4200ngg(-1)), and even higher levels were observed in plants. Principal component analysis of selected ion chromatograms of PAHs showed a clear separation of plants vs. sediments. The plants preferentially accumulated the high molecular PAHs, both from sedimentation ponds with a petrogenic PAH isomer ratio in sediments; and from a lake with pyrogenic PAH isomer ratio in sediments. PMID:27267726

  17. COMPARISON OF BIOMARKERS IN WORKERS EXPOSED TO 2,4,6-TRINITROTOLUENE

    EPA Science Inventory

    2,4,6-Trinitrotoluene (TNT) is an important occupational and environmental pollutant. In TNT-exposed humans, the notable toxic manifestations have included aplastic anemia, toxic hepatitis, cataracts, hepatomegaly, and liver cancer. Therefore, we developed methods to biomonitor w...

  18. Measured and predicted affinities of binding and relative potencies to activate the AhR of PAHs and their alkylated analogues.

    PubMed

    Lee, Sangwoo; Shin, Woong-Hee; Hong, Seongjin; Kang, Habyeong; Jung, Dawoon; Yim, Un Hyuk; Shim, Won Joon; Khim, Jong Seong; Seok, Chaok; Giesy, John P; Choi, Kyungho

    2015-11-01

    Polycyclic aromatic hydrocarbons (PAHs) and their alkylated forms are important components of crude oil. Both groups of PAHs have been reported to cause dioxin-like responses, mediated by aryl hydrocarbon receptor (AhR). Thus, characterization of binding affinity to the AhR of unsubstituted or alkylated PAHs is important to understand the toxicological consequences of oil contamination on ecosystems. We investigated the potencies of major PAHs of crude oil, e.g., chrysene, phenanthrene and dibenzothiophene, and their alkylated forms (n=17) to upregulate expression of AhR-mediated processes by use of the H4IIE-luc transactivation bioassay. In addition, molecular descriptors of different AhR activation potencies among PAHs were investigated by use of computational molecular docking models. Based on responses of the H4IIE-luc in vitro assay, it was shown that potencies of PAHs were determined by alkylation in addition to the number and conformation of rings. Potencies of AhR-mediated processes were generally greater when a chrysene group was substituted, especially in 1-methyl-chrysene. Significant negative correlations were observed between the in vitro dioxin-like potency measured in H4IIE-luc cells and the binding distance estimated from the in silico modeling. The difference in relative potency for AhR activation observed among PAHs and their alkylated forms could be explained by differences among binding distances in the ligand binding domain of the AhR caused by alkylation. The docking model developed in the present study may have utility in predicting risks of environmental contaminants of which toxicities are mediated by AhR binding. PMID:26037956

  19. Formation of Polycyclic Aromatic Hydrocarbons exhibiting (5,7)-member ring defects in Planetary Nebulae

    NASA Astrophysics Data System (ADS)

    Öttl, S.; Huber, S. E.; Kimeswenger, S.; Probst, M.

    2014-04-01

    Polycyclic aromatic hydrocarbons (PAHs) are nowadays widely accepted as one of the carriers of the ubiquitous aromatic infrared (IR) bands. The IR spectra of many planetary nebulae (PNe) are dominated by mid-IR emission features, attributed to the IR fluorescence of PAHs. Recent observations of PNe show the simultaneous presence of mid-IR features attributed to neutral fullerene molecules (i.e. C60) and PAHs (García-Hernández et al. 2010). In general, PNe show evidence of mixed chemistry with emission from PAHs, silicate dust, fullerenes and contributions from other molecular components. The still unidentified IR features seen in PNe require further laboratory and observational investigations. We present a theoretical study of the IR spectra of PAHs containing (5,7)-member ring defects. Using density functional theory, we investigate the effects such defects have on the IR spectra of pyrene (C16H10) and coronene (C24H12). In addition, we explore parts of the potential energy surface of the neutral species and discuss alternative formation pathways, especially in the environment of PNe. Coronene and pyrene can be seen as limiting or prototypical cases in various respects. They are among the smallest hydrocarbons that can exhibit (5,7)-ring defects. Previous work (Yu et al. 2012) has raised the suspicion that effects of such defects might be more intriguing with decreasing size of the PAHs. Our investigations represent the limiting cases with respect to the size of the PAHs. To study these small systems is thought to be an important step towards a substantial understanding of the role of (5,7)-ring defects for the IR spectra of PAHs. The formation of these (5,7)-ring defects in PAHs may be well supported in PNe. The environment strongly enables the transition from the ground state to the defect state. Therefore the knowledge of the IR spectra of these molecules will support the investigations in understanding the unidentified IR emission bands in PNe.

  20. Saturn's Spectacular Ring System

    NASA Technical Reports Server (NTRS)

    Lissauer, Jack J.; DeVincenzi, Donald (Technical Monitor)

    2001-01-01

    Saturn's beautiful rings have fascinated astronomers since they were first observed by Galileo in 1610. The main rings consist of solid particles mostly in the 1 cm - 10 m range, composed primarily of water ice. The ring disk is exceptionally thin - the typical local thickness of the bright rings is tens of meters, whereas the diameter of the main rings is 250,000 km! The main rings exhibit substantial radial variations "ringlets", many of which are actively maintained via gravitational perturbations from Saturn's moons. Exterior to the main rings lie tenuous dust rings, which have little mass but occupy a very large volume of space. This seminar will emphasize the physics of ring-moon interactions, recent advances in our understanding of various aspects of the rings obtained from observations taken during 1995 when the rings appeared edge-on to the Earth and then to the Sun, and observations in subsequent years from HST.

  1. Spiro[2.4]hepta-4,6-dienes: synthesis and application in organic synthesis

    NASA Astrophysics Data System (ADS)

    Menchikov, L. G.; Nefedov, O. M.

    2016-03-01

    This review integrates and describes systematically the data in the field of spiro[2.4]hepta-4,6-dienes published in the past 15 years. The changes in the development of studies that took place during this period are noted. The methods for the synthesis, the reactivity details and key chemical transformations of spiro[2.4]hepta-4,6-dienes are considered, with the emphasis on applications of these compounds in organic synthesis. The bibliography includes 207 references.

  2. Synthesis of Heteroaryl Sulfonamides from Organozinc Reagents and 2,4,6-Trichlorophenyl Chlorosulfate

    PubMed Central

    2016-01-01

    A method for the preparation of aryl and heteroaryl sulfonamides using 2,4,6-trichlorophenyl chlorosulfate (TCPC) is described. The reaction of 2-pyridylzinc reagents with TCPC resulted in 2,4,6-trichlorophenyl (TCP) pyridine-2-sulfonates, and the parent pyridine-2-sulfonate was shown to react with amines. Less electron-rich aryl- and heteroarylzinc reagents reacted with TCPC to afford sulfonyl chlorides that were converted in situ to sulfonamides. PMID:26065317

  3. Assessing risks to adults and preschool children posed by PM2.5-bound polycyclic aromatic hydrocarbons (PAHs) during a biomass burning episode in Northern Thailand.

    PubMed

    Pongpiachan, Siwatt; Tipmanee, Danai; Khumsup, Chukkapong; Kittikoon, Itthipon; Hirunyatrakul, Phoosak

    2015-03-01

    To investigate the potential cancer risk resulting from biomass burning, polycyclic aromatic hydrocarbons (PAHs) bound to fine particles (PM2.5) were assessed in nine administrative northern provinces (NNP) of Thailand, before (N-I) and after (N-II) a haze episode. The average values of Σ 3,4-ring PAHs and B[a] P Equivalent concentrations in world urban cities were significantly (p<0.05) much higher than those in samples collected from northern provinces during both sampling periods. Application of diagnostic binary ratios of PAHs underlined the predominant contribution of vehicular exhaust to PM2.5-bound PAH levels in NNP areas, even in the middle of the agricultural waste burning period. The proximity of N-I and N-II values in three-dimensional (3D) principal component analysis (PCA) plots also supports this conclusion. Although the excess cancer risk in NNP areas is much lower than those of other urban area and industrialized cities, there are nevertheless some concerns relating to adverse health impacts on preschool children due to non-dietary exposure to PAHs in home environments. PMID:25506906

  4. PAH emissions from coal combustion and waste incineration.

    PubMed

    Hsu, Wei Ting; Liu, Mei Chen; Hung, Pao Chen; Chang, Shu Hao; Chang, Moo Been

    2016-11-15

    The characteristics of PAHs that are emitted by a municipal waste incinerator (MWI) and coal-fired power plant are examined via intensive sampling. Results of flue gas sampling reveal the potential for PAH formation within the selective catalytic reduction (SCR) system of a coal-fired power plant. In the large-scale MWI, the removal efficiency of PAHs achieved with the pilot-scaled catalytic filter (CF) exceeds that achieved by activated carbon injection with a bag filter (ACI+BF) owing to the effective destruction of gas-phase contaminants by a catalyst. A significantly lower PAH concentration (1640ng/g) was measured in fly ash from a CF module than from an ACI+BF system (5650ng/g). Replacing the ACI+BF system with CF technology would significantly reduce the discharge factor (including emission and fly ash) of PAHs from 251.6 to 77.8mg/ton-waste. The emission factors of PAHs that are obtained using ACI+BF and the CF system in the MWI are 8.05 and 7.13mg/ton, respectively. However, the emission factor of MWI is significantly higher than that of coal-fired power plant (1.56mg/ton). From the perspective of total environmental management to reduce PAH emissions, replacing the original ACI+BF process with a CF system is expected to reduce environmental impact thereof. PMID:27391862

  5. Annual variability of PAH concentrations in the Potomac River watershed

    SciTech Connect

    Maher, I.L.; Foster, G.D.

    1995-12-31

    Dynamics of organic contaminant transport in a large river system is influenced by annual variability in organic contaminant concentrations. Surface runoff and groundwater input control the flow of river waters. They are also the two major inputs of contaminants to river waters. The annual variability of contaminant concentrations in rivers may or may not represent similar trends to the flow changes of river waters. The purpose of the research is to define the annual variability in concentrations of polycyclic aromatic hydrocarbons (PAH) in riverine environment. To accomplish this, from March 1992 to March 1995 samples of Potomac River water were collected monthly or bimonthly downstream of the Chesapeake Bay fall line (Chain Bridge) during base flow and main storm flow hydrologic conditions. Concentrations of selected PAHs were measured in the dissolved phase and the particulate phase via GC/MS. The study of the annual variability of PAH concentrations will be performed through comparisons of PAH concentrations seasonally, annually, and through study of PAH concentration river discharge dependency and rainfall dependency. For selected PAHs monthly and annual loadings will be estimated based on their measured concentrations and average daily river discharge. The monthly loadings of selected PAHs will be compared by seasons and annually.

  6. Decontamination of soils containing PAHs by electroremediation: a review.

    PubMed

    Pazos, M; Rosales, E; Alcántara, T; Gómez, J; Sanromán, M A

    2010-05-15

    During the last years, the anthropogenic sources have contributed to organic compound penetration into the environment. One large group of persistent and toxic contaminants is the hydrophobic organic contaminants. Among them, polycyclic aromatic hydrocarbons (PAHs) have been recognized as a representative group of these pollutants with low solubility. In this paper, it is showed the electroremediation of soil contaminated with PAHs as an alternative, to organic compound removal. This technique, mainly used for heavy metal extraction, applies the electric current to promote the movement of contaminants. Nowadays the application of this technique alone or combined with other techniques as for example Fenton or bioremediation is taking fine results to PAHs removal. Although the PAHs soil decontamination by means of the electric field is in an initial stage, many researchers have demonstrated the treatment effectiveness. This paper describes the foremost principles to carry out the electroremediation of soils contaminated with PAHs, just like the different alternatives to improve the electroremediation of PAHs and also the new methodologies of PAHs removal by using hybrid technologies. PMID:20006434

  7. Inhibitory activities against rice pathogens of 8-hydroxy-2,4,6-octatriynamide from Agrocybe sp.

    PubMed

    Zheng, Yongbiao; Xu, Xiaoping; Wu, Yabin

    2016-03-01

    8-Hydroxy-2,4,6-octatriynamide, a natural polyacetylene with inhibitory activities against rice pathogens, was isolated from the liquid fermentation broth of strain Agrocybe sp. YB2005 during screening for new natural chemical agents to control rice pathogens. 8-hydroxy-2,4,6-octatriynamide was purified by consecutive chromatography over a Cl8 reversed phase silica gel, sephadex LH-20 and silica gel. The chemical structure of 8-hydroxy-2,4,6-octatriynamide was elucidated through spectroscopic analyses, including 1D- and 2D-NMR, ESI mass spectrometry and X-ray single crystal diffraction. Bioassays showed that 8-hydroxy-2,4,6-octatriynamide could significantly inhibit growth of Xanthomonas oryzae with an MIC of 53.1 μM in a 96-well plate and the growth of Rhizoctonia solani at 1.02 mM in a 24-well plate. When rice leaves were inoculated with Magnaporthe grisea and cultured in artificial nutrition liquid containing 0.34 mM 8-hydroxy-2,4,6-octatriynamide, no rice blast was observed. The present study implied that 8-hydroxy-2,4,6-octatriynamide could be a candidate agent against rice pathogens. PMID:26861586

  8. Access to 4,6-Diarylpicolinates via a Domino Reaction of Cyclic Sulfamidate Imines with Morita-Baylis-Hillman Acetates of Nitroolefins/Nitrodienes.

    PubMed

    Majee, Debashis; Biswas, Soumen; Mobin, Shaikh M; Samanta, Sampak

    2016-05-20

    An interesting domino reaction of 5-membered cyclic sulfamidate imines with a variety of Morita-Baylis-Hillman acetates of nitroolefins/nitrodienes in the presence of DABCO as an organic base at 55 °C is reported for the first time. This new synthetic strategy provides a series of pharmacologically interesting 4,6-diarylpicolinates in high to excellent yields and allows several compatible functionalities on aryl rings. Moreover, the biologically interesting imidazo[1,2-a]pyridine (alpidem derivative) has been prepared in high chemical yield through a unique procedure. PMID:27129356

  9. Photoinduced degradation of PAHs in the presence of ozone

    SciTech Connect

    Schutt, W.S.; Li, Y.; Sigman, M.E. |

    1995-12-31

    Polycyclic Aromatic Hydrocarbons (PAH) are formed from both anthropogenic and natural sources. In order to assess the environmental impact caused by the surface-adsorbed PAHs, the chemical lifetimes of these compounds in the atmosphere must be determined. Although ozone is known to be a primary reactant in the chemical transformation of surface-adsorbed PAHs in the atmosphere, the kinetics of these reactions have not been investigated in detail. In addition to the experimental difficulties that arise in using an oxygen-ozone stream while monitoring the PAH with fluorescence, complications in analyzing the kinetic mechanism also exist. It is difficult to determine whether the ozone or oxygen initially quenches the excited state of PAH. Ozone could enhance the degradation rate by simply reacting with a product derived from the excited state of PAH and oxygen. The focus of this study is to demonstrate the use of fluorescence spectroscopy in monitoring the degradation of PAH adsorbed on a three dimensional particle in the presence of gaseous ozone free from the interference of oxygen. More specifically, the experimental procedure will involve the generation of an ozone-nitrogen gas stream to be used in the investigation of dark and photochemical reactions between ozone and naphthalene. The absence of oxygen in the system will allow for the accurate monitoring of PAH fluorescence decay due solely to ozone quenching. It will also aid in the determination of the reaction mechanism. This is the first time that the direct interaction of ozone with an excited state of PAH has been demonstrated.

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

    PubMed Central

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

    2007-01-01

    Bioaugmentation of soil polluted with polycyclic aromatic hydrocarbons (PAHs) is often disappointing because of the low survival rate and low activity of the introduced degrader bacteria. We therefore investigated the possibility of priming PAH degradation in soil by adding 2% of bioremediated soil with a high capacity for PAH degradation. The culturable PAH-degrading community of the bioremediated primer soil was dominated by Mycobacterium spp. A microcosm containing pristine soil artificially polluted with PAHs and primed with bioremediated soil showed a fast, 100- to 1,000-fold increase in numbers of culturable phenanthrene-, pyrene-, and fluoranthene degraders and a 160-fold increase in copy numbers of the mycobacterial PAH dioxygenase gene pdo1. A nonpolluted microcosm primed with bioremediated soil showed a high rate of survival of the introduced degrader community during the 112 days of incubation. A nonprimed control microcosm containing pristine soil artificially polluted with PAHs showed only small increases in the numbers of culturable PAH degraders and no pdo1 genes. Initial PAH degradation rates were highest in the primed microcosm, but later, the degradation rates were comparable in primed and nonprimed soil. Thus, the proliferation and persistence of the introduced, soil-adapted degraders had only a marginal effect on PAH degradation. Given the small effect of priming with bioremediated soil and the likely presence of PAH degraders in almost all PAH-contaminated soils, it seems questionable to prime PAH-contaminated soil with bioremediated soil as a means of large-scale soil bioremediation. PMID:17209064

  11. Heterogeneous Reactions of Chinese Particulate Matter with O3, OH radicals and N2O5 to Simulate Trans-Pacific Atmospheric Transport of PAHs

    NASA Astrophysics Data System (ADS)

    Simonich, S. L.; Jariyasopit, N.; Zimmermann, K.; Schrlau, J.; Arey, J.; Atkinson, R.

    2011-12-01

    In the atmosphere, polycyclic aromatic hydrocarbons (PAHs) partition between the gas and particulate phases depending on their chemical and physical properties and ambient temperature. In general, PAHs with more than four aromatic rings are found primarily in the particulate phase, allowing them to undergo long range atmospheric transport. The reactivity of particulate-bound PAHs is considered to vary, to some extent, with the composition of particle. Previous heterogeneous reaction studies on particulate matter (PM) have used graphite, diesel soot, wood smoke and in-house soot samples. However, in this study, PM from Beijing, China, with an aerodynamic diameter < 10 μm, was exposed to O3, OH radicals, and N2O5 to simulate heterogeneous reactions that may occur during trans-Pacific transport. The PM samples were collected on pre-baked quartz fiber filters over 24 h periods at an urban site in Beijing, China. The filters were cut into two portions. The first portion was quantitatively analyzed for PAHs, nitrated-PAHs (NPAHs) and oxygenated-PAHs (OPAHs) and represented the unreacted masses. The second portion was placed in a ~7000-L indoor all-Teflon chamber and exposed to either O3, OH radicals, or N2O5. The concentrations of O3, OH radicals, and N2O5 used in chamber experiments, combined with the duration of the exposures, simulated trans-Pacific atmospheric transport of the PM. The quantitative analysis of both the unreacted and reacted portions of the filter was done using gas chromatography coupled with mass spectrometry, with electron ionization for PAHs and negative chemical ionization mode for NPAHs and OPAHs. The reaction of PAHs on PM with O3 resulted in a 16% - 48% loss in parent PAH concentrations. As expected, no significant NPAH products were observed in the O3 reaction. For the OH-radical exposure, the parent PAH masses on PM decreased by 1% to 42%. Only 1-nitropyrene and 6-nitrobenzo[a]pyrene concentrations were found to increase significantly, while

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

    PubMed

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

    2016-01-01

    We have analyzed a set of 51 PAHs whose structures have been hypothesized from mass spectrometry data collected on samples extracted from carbon particles of combustion origin. We have obtained relationships between infrared absorption signals in the fingerprint region (mid-IR) and the chemical structures of PAHs, thus proving the potential of IR spectroscopy for the characterization of the molecular structure of aromatic combustion products. The results obtained here for the spectroscopic characterization of PAHs can be also of interest in Materials Science and Astrophysics. PMID:26208268

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

    NASA Astrophysics Data System (ADS)

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

    2016-01-01

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

  14. High-spectral resolution observations of the 3.29 micron emission feature: Comparison to QCC and PAHs

    NASA Technical Reports Server (NTRS)

    Tokunaga, Alan T.; Sellgren, Kris; Sakata, Akira; Wada, S.; Onaka, Takashi; Nakada, Y.; Nagata, T.

    1989-01-01

    Two of the most promising explanations for the origin of the interstellar emission features observed at 3.29, 3.4, 6.2, 7.7, 8.6, and 11.3 microns are: quenched carbonaceous composite (QCC) and polycyclic aromatic hydrocarbons (PAHs). High resolution spectra are given of the 3.29 micron emission feature which were taken with the Cooled Grating Array Spectrometer at the NASA Infrared Telescope Facility and previously published. These spectra show that the peak wavelength of the 3.29 micron feature is located at 3.295 + or - 0.005 micron and that it is coincident with the peak absorbance of QCC. The peak wavelength of the 3.29 micron feature appears to be the same in all of the sources observed thus far. However, the width of the feature in HD 44179 and Elias 1 is only 0.023 micron, which is smaller than the 0.043 micron width in NGC 7027, IRAS 21282+5050, the Orion nebula, and BD+30 deg 3639. Spectra of NGC 7027, QCC, and PAHs is shown. QCC matches the 3.29 micron interstellar emission feature very closely in the wavelength of the peak, and it produces a single feature. On the other hand, PAHs rarely match the peak of the interstellar emission feature, and characteristically produce multiple features.

  15. Stirling engine piston ring

    DOEpatents

    Howarth, Roy B.

    1983-01-01

    A piston ring design for a Stirling engine wherein the contact pressure between the piston and the cylinder is maintained at a uniform level, independent of engine conditions through a balancing of the pressure exerted upon the ring's surface and thereby allowing the contact pressure on the ring to be predetermined through the use of a preloaded expander ring.

  16. Polycyclic aromatic hydrocarbons (PAHs) and alkylated PAHs in the coastal seawater, surface sediment and oyster from Dalian, Northeast China.

    PubMed

    Hong, Wen-Jun; Jia, Hongliang; Li, Yi-Fan; Sun, Yeqing; Liu, Xianjie; Wang, Luo

    2016-06-01

    A total of 46 polycyclic aromatic hydrocarbons (PAHs, 21 parent and 25 alkylated) were determined in seawater, surface sediment and oyster from coastal area of Dalian, North China. The concentration of Σ46PAHs in seawater, sediment, and oyster were 136-621 ng/L, 172-4700 ng/g dry weight (dw) and 60.0-129 ng/g wet weight (ww) in winter, and 65.0-1130 ng/L, 71.1-1090 ng/g dw and 72.8-216 ng/g ww in summer, respectively. High PAH levels were found in industrial area both in winter and summer. Selected PAH levels in sediments were compared with Sediments Quality Guidelines (ERM-ERL, TEL-PEL indexes) for evaluation probable toxic effects on marine organism and the results indicate that surface sediment from all sampling sites have a low to medium ecotoxicological risk. Daily intake of PAHs via oyster as seafood by humans were estimated and the results indicated that oyster intake would not pose a health risk to humans even 30 days after a oil spill accident near by. Water-sediment exchange analysis showed that, both in winter and summer, the fluxes for most high molecular weight PAHs were from seawater to sediment, while for low molecular weight PAHs, an equilibrium was reached between seawater and sediment. PMID:26874984

  17. Behavior of PAH/mineral associations during thermodesorption: impact for the determination of mineral retention properties towards PAHs.

    PubMed

    Biache, Coralie; Lorgeoux, Catherine; Saada, Alain; Faure, Pierre

    2015-05-01

    Polycyclic aromatic hydrocarbons (PAHs) associated with two minerals (silica sand and bentonite) presenting opposite retention properties were analyzed with a thermodesorption (Td)-GC-MS coupling in order to validate this technique as a new and rapid way to evaluate the solid sorption properties. Two analysis modes were used, evolved gas analysis (EGA) and Td with cryo-trap. EGA allowed a real-time monitoring of the compounds desorbed during a temperature program and gave a first screening of the samples while Td gave more precise indications on compound abundances for selected temperature ranges. When associated with silica sand, PAHs were released at relatively low temperatures (<300 °C) close to corresponding boiling point, whereas for the PAH/bentonite mixture, PAHs were desorbed at much higher temperatures; they were also present in much lower abundance and were associated with mono-aromatic compounds. With bentonite, the PAH abundances decreased and the mono-aromatics increased with the increasing PAH molecular weight. These results indicated a clear PAH retention by the bentonite due to polymerization, followed by a thermal cracking at higher temperatures. The Td-GC-MS was proven to efficiently underline differences in retention properties of two minerals, and this study highlights the great potential of this technique to evaluate compound/matrix bond strength and interaction. PMID:25772555

  18. Actin Rings of Power.

    PubMed

    Schwayer, Cornelia; Sikora, Mateusz; Slováková, Jana; Kardos, Roland; Heisenberg, Carl-Philipp

    2016-06-20

    Circular or ring-like actin structures play important roles in various developmental and physiological processes. Commonly, these rings are composed of actin filaments and myosin motors (actomyosin) that, upon activation, trigger ring constriction. Actomyosin ring constriction, in turn, has been implicated in key cellular processes ranging from cytokinesis to wound closure. Non-constricting actin ring-like structures also form at cell-cell contacts, where they exert a stabilizing function. Here, we review recent studies on the formation and function of actin ring-like structures in various morphogenetic processes, shedding light on how those different rings have been adapted to fulfill their specific roles. PMID:27326928

  19. New Dust Belts of Uranus: One Ring, Two Ring, Red Ring, Blue Ring

    SciTech Connect

    de Pater, I; Hammel, H B; Gibbard, S G; Showalter, M R

    2006-02-02

    We compare near-infrared observations of the recently discovered outer rings of Uranus with HST results. We find that the inner ring, R/2003 U 2, is red, whereas the outer ring, R/2003 U 1, is very blue. Blue is an unusual color for rings; Saturn's enigmatic E ring is the only other known example. By analogy to the E ring, R/2003 U 1 is probably produced via impacts into the embedded moon Mab, which apparently orbits at a location where non-gravitational perturbations favor the survival and spreading of sub-micron sized dust. R/2003 U 2 more closely resembles Saturn's G ring.

  20. Polycyclic aromatic hydrocarbons (PAH) and their genotoxicity in exhaust emissions from a diesel engine during extended low-load operation on diesel and biodiesel fuels

    NASA Astrophysics Data System (ADS)

    Vojtisek-Lom, Michal; Pechout, Martin; Dittrich, Luboš; Beránek, Vít; Kotek, Martin; Schwarz, Jaroslav; Vodička, Petr; Milcová, Alena; Rossnerová, Andrea; Ambrož, Antonín; Topinka, Jan

    2015-05-01

    This paper investigates the effects of emissions including carcinogenic polycyclic aromatic hydrocarbons (cPAH) of a conventional diesel engine without a particle filter. Experiments were carried on during extended idle and during a loaded operation immediately following the extended idle. Extended low-load operation of diesel engines due to idling and creep at border crossings, loading areas and in severe congestion has been known to deteriorate the combustion and catalytic device performance and to increase the emissions of particulate matter (PM). A conventional diesel engine was coupled to a dynamometer and operated on diesel fuel and neat biodiesel alternately at idle speed and 2% of rated power and at 30% and 100% load at intermediate speed. Exhaust was sampled on fiber filters, from which the content of elemental and organic carbon and polycyclic aromatic hydrocarbons (PAH), including cPAH and benzo[a]pyrene (B[a]P) have been determined. The emissions of cPAH and B[a]P have increased 4-6 times on diesel fuel and by 4-21% on biodiesel during extended idling relative to a short idle and 8-12 times on diesel fuel and 2-20 times on biodiesel during subsequent operation at full load relative to stabilized operation at full load. The total "excess" cPAH emissions after the transition to full load were on the same order of magnitude as the total "excess" cPAH during extended idling. The absolute levels of PAH, cPAH and B[a]P emissions under all operating conditions were lower on biodiesel compared to diesel fuel. Genotoxicity of organic extracts of particles was analysed by acellular assay with calf thymus DNA (CT-DNA) and was consistently higher for diesel than for biodiesel. The exhaust generated during extended idle and subsequent full load exhibited the highest genotoxicity for both fuels. These two regimes are characterized by significant formation of cPAH as well as other DNA reactive compounds substantially contributing to the total genotoxicity. Oxidative

  1. PAHs, PAH-induced carcinogenic potency, and particle-extract-Induced cytotoxicity of traffic-related nano/ultrafine particles.

    PubMed

    Lin, Chih-Chung; Chen, Shui-Jen; Huang, Kuo-Lin; Lee, Wen-Jhy; Lin, Wen-Yinn; Tsai, Jen-Hsiung; Chaung, Hso-Chi

    2008-06-01

    Polycyclic aromatic hydrocarbons (PAHs) bound in nano/ ultrafine particles from vehicle emissions may cause adverse health effects. However, little is known about the characteristics of the nanoparticle-bound PAHs and the PAH-associated carcinogenic potency/cytotoxicity; therefore, traffic-related nano/ultrafine particles were collected in this study using a microorifice uniform deposition impactor(MOUDI) and a nano-MOUDI. For PM0.056--18, the difference in size-distribution of particulate total-PAHs between non-after-rain and after-rain samples was statistically significant at alpha = 0.05; however, this difference was not significant for PM0.01--0.056. The PAH correlation between PM0.01--0.1 and PM0.1--1.8 was lower for the after-rain samples than forthe non-after-rain samples. The average particulate total-PAHs in five samplings displayed a trimodal distribution with a major peak in the Aitken mode (0.032--0.056 microm). About half of the particulate total-PAHs were in the ultrafine size range. The BaPeq sums of BaP, IND, and DBA (with toxic equivalence factors > or = 0.1) accounted for approximately 90% of the total-BaPeq in the nano/ultrafine particles, although these three compounds contributed little to the mass of the sampled particles. The mean content of the particle-bound total-PAHs/-BaPeqs and the PAH/BaPeq-derived carcinogenic potency followed the order nano > ultrafine > fine > coarse. For a sunny day sample, the cytotoxicity of particle extracts (using 1:1 (v/v) n-hexane/dichloromethane) was significantly higher (p < 0.05) for the nano (particularly the 10-18 nm)/ultrafine particles than for the coarser particles and bleomycin. Therefore, traffic-related nano and ultrafine particles are possibly cytotoxic. PMID:18589992

  2. Searches for Ring Organics in Carbon-Rich Evolved Stars and Hot Molecular Cores

    NASA Astrophysics Data System (ADS)

    Kuan, Y.-J.; Huang, H.-C.; Charnley, S. B.; Butner, H. M.; Lee, Y.-Y.; Despois, D.; Botta, O.; Kisiel, Z.; Ehrenfreund, P.; Markwick, A. J.

    It has been proposed that polycyclic aromatic hydrocarbons (PAHs) are ubiquitously distributed in the interstellar medium. PAHs are also known widespread in meteorites. AGBs and post-AGBs are copious producers of carbonaceous dust particles. Interstellar PAHs, and those found in meteorites, probably originated in the cool circumstellar envelopes (CSEs) of carbon stars. Current astrochemical theories of PAH formation around C-rich red giant stars are based on acetylene (C_2H_2) polymerization. Nitrogen-heterocycles are known to be present in meteoritic material, and there is growing evidence that N-heterocycles could be an important component of the interstellar PAH population. In particular, as hydrogen cyanide (HCN) is abundant in CSEs of C-stars, an HCN addition in the sequence that leads to benzene (C_6H_6) can instead lead to Pyridine (c-C_5H_5N). Substitution of nitrogen atoms for two carbon atoms in a benzene ring yields Pyrimidine c-C_4H_4N_2. Acetylene polymerization of Pyridine, or HCN addition to the phenyl radical (C_6H_5), can likewise lead to Quinoline and Isoquinoline, C_9H_7N. We have thus conducted an extensive astronomical search for N-bearing interstellar rings Quinoline, Isoquinoline and Pyridine toward carbon-rich CSEs, and Pyrimidine in hot molecular cores. In this report, we will briefly summarize the status of our searches.

  3. Sorption and chemical transformation of PAHs on coal fly ash. Final technical report

    SciTech Connect

    Mamantov, G.; Wehry, E.L.

    1995-02-01

    The objectives of this work were to characterize the interactions of coal fly ash with polycyclic aromatic hydrocarbons (PAH`s) and their derivatives, and to attempt to understand the influence of surface properties of coal ash in the chemical transformations of PAH`s.

  4. Antimony(III) complexes with 2-amino-4,6-dimethoxypyrimidines: Synthesis, characterization and biological evaluation.

    PubMed

    Tunç, Turgay; Karacan, Mehmet Sayım; Ertabaklar, Hatice; Sarı, Musa; Karacan, Nurcan; Büyükgüngör, Orhan

    2015-12-01

    Novel pyrimidine compound bearing disulfide bridge, 5,5'-disulfanediylbis(2-amino-4,6-dimetoxypyrimidine) (3) was synthesized by reduction of 2-amino-4,6-dimethoxy-5-thiocyanatopyrimidine for the first time, and its structure was confirmed by X-ray crystallographic analysis. Novel binuclear antimony(III) compound of (3), {Sb[5,5'-disulfanediylbis(2-amino-4,6-dimetoxypyrimidine)]Cl3}2 (4) and mononuclear antimony(III) compounds, SbL2Cl3, [L: 2-amino-5-thiol-4,6-dimethoxy pyrimidine (2) and 2-amino-5-(1H-tetrazol-5-ylthio)-4,6-dimethoxypyrimidine (6)] were synthesized and characterized with the help of elemental analysis, molecular conductivity, FT-IR, (1)H-NMR and LC-MS techniques. The geometrical structures optimized by a DFT/B3LYP/LANL2DZ method of the compounds, indicated that monomeric compounds have square pyramidal shape. Both antileishmanial activity against Leishmania tropica promastigote and glutathione reductase inhibitory activity were determined in vitro. The results showed that (3) has the best biological activity. PMID:26427018

  5. Assessing PAH exposure in feral finfish from the Northwest Atlantic.

    PubMed

    Hellou, J; Leonard, J; Collier, T K; Ariese, F

    2006-04-01

    Polycyclic aromatic hydrocarbon (PAH) concentrations were examined in small finfish (<30 cm) represented by capelin, sand lance, American plaice, yellowtail flounder and herring collected opportunistically in various NAFO divisions. Analyses were performed on whole fish and in a portion of the samples; concentrations in internal organs were compared to the rest of the carcass. The effect of pool size, size differences within and between species, lipid content and location were examined to interpret PAH concentrations. Measurements were carried out before the development of the Hibernia oil fields and represent baseline levels for future comparison. Limits in assessing future risk that could be due to discharges of produced water or accidental oil spills are also discussed. Increasing knowledge on the bioaccumulation of PAH, on the production of bile metabolites, the formation of DNA-adducts and of the potential toxic effects associated with PAH will lead to better ecosystem management and protection for future generations. PMID:16364371

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

    PubMed

    Ciemniak, Artur; Chrachol, Lucyna

    2008-01-01

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

  7. Effects of PAHs on the feeding activity of tubificid worms

    SciTech Connect

    Lotufo, G.R.

    1994-12-31

    Sediment collected from a clean site in LA was sieved through a 125{mu}m screen and contaminated with individual PAHs (pyrene, phenanthrene and dibenzofuran) at increasing concentrations using spiking procedure and with a mixture of the 3 PAHs at a single concentration by shell coating. Feeding activity was estimated by defecation rate. Groups of 15 worms were assigned to defecation chambers in 4 replicates per treatment. Feces were collected daily for 10 days, filtered through a 8{mu}m membrane filter and dry weight measured. Results obtained with phenanthrene and mixture of 3 PAHs indicate that PHA bulk concentration of 100 mg/dry kg and higher significantly reduce tubificid ingestion of sediment. Total recovery to control levels occurred when worms exposed to high concentration of PAH were transferred to clean sediment. Total OC was determined to be 3.2 %.

  8. Deuterium Enrichment of PAHs by VUV Irradiation of Interstellar Ices

    NASA Technical Reports Server (NTRS)

    Bernstein, Max P.; Sandford, Scott A.; Allamandola, Louis J.; Gillette, J. Seb; Zare, Richard N.; DeVincenzi, Donald (Technical Monitor)

    1998-01-01

    Laboratory results demonstrate that polycyclic aromatic hydrocarbons (PAHs) rapidly exchange their hydrogen atoms with those of nearby molecules when they are frozen into low-temperature ices and exposed to vacuum ultraviolet radiation. As a result, PAHs quickly become deuterium-enriched when VUV irradiated in D-containing ices. This mechanism has important consequences for several astrophysical issues owing to the ubiquitous nature of PAHs in the interstellar medium. For example, this process may explain the deuterium enrichments found in PAHs in meteorites and interplanetary dust particles. These results also provide general predictions about the molecular siting of the deuterium on aromatic materials in meteorites if this process produced a significant fraction of their D-enrichment.

  9. 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...

  10. DISSIPATION OF PAHs IN SATURATED, DREDGED SEDIMENTS: A FIELD TRIAL

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Sediments dredged from navigable rivers often contain elevated concentrations of recalcitrant, potentially toxic organic compounds such as polychlorinated biphenyls (PCBs) and polyaromatic hydrocarbons (PAHs). The presence of these compounds often requires that the sediments be stored in fully conta...

  11. Pore Water PAH Transport in Amended Sediment Caps

    NASA Astrophysics Data System (ADS)

    Gidley, P. T.; Kwon, S.; Ghosh, U.

    2009-05-01

    Capping is a common remediation strategy for contaminated sediments that creates a physical barrier between contaminated sediments and the water column. Diffusive flux of contaminants through a sediment cap is small. However, under certain hydrodynamic conditions such as groundwater potential and tidal pumping, groundwater advection can accelerate contaminant transport. Hydrophobic organic contaminants such as polycyclic aromatic hydrocarbons (PAHs) could be transported through the cap under advective conditions. To better understand PAH migration under these conditions, physical models of sediment caps were evaluated in the laboratory through direct measurement of pore water using solid phase micro-extraction with gas chromatography and mass spectrometry. Contaminated sediment and capping material was obtained from an existing Superfund site that was capped at Eagle Harbor, Washington. A PAH dissolution model linked to an advection-dispersion equation with retardation using published organic carbon-water partitioning coefficients (Koc) was compared to measured PAHs in the sediment and cap porewater of the physical model.

  12. Enhanced PM10 bounded PAHs from shipping emissions

    NASA Astrophysics Data System (ADS)

    Pongpiachan, S.; Hattayanone, M.; Choochuay, C.; Mekmok, R.; Wuttijak, N.; Ketratanakul, A.

    2015-05-01

    Earlier studies have highlighted the importance of maritime transport as a main contributor of air pollutants in port area. The authors intended to investigate the effects of shipping emissions on the enhancement of PM10 bounded polycyclic aromatic hydrocarbons (PAHs) and mutagenic substances in an industrial area of Rayong province, Thailand. Daily PM10 speciation data across two air quality observatory sites in Thailand during 2010-2013 were collected. Diagnostic binary ratios of PAH congeners, analysis of variances (ANOVA), and principal component analysis (PCA) were employed to evaluate the enhanced genotoxicity of PM10 during the docking period. Significant increase of PAHs and mutagenic index (MI) of PM10 were observed during the docking period in both sampling sites. Although stationary sources like coal combustions from power plants and vehicular exhausts from motorway can play a great role in enhancing PAH concentrations, regulating shipping emissions from diesel engine in the port area like Rayong is predominantly crucial.

  13. Investigation into atmospheric PM2.5-borne PAHs in Eastern cities of China: concentration, source diagnosis and health risk assessment.

    PubMed

    Li, Ye; Liu, Xinran; Liu, Min; Li, Xiaofei; Meng, Fei; Wang, Juan; Yan, Wenjun; Lin, Xianbiao; Zhu, Junmin; Qin, Yukun

    2016-05-18

    This study investigated PM2.5-PAHs associations collected in Beijing, Jinan, and Shanghai in Eastern China. The results indicated that PM2.5 concentrations in Beijing, Jinan, and Shanghai were 125.7 μg m(-3) (18.6-355.5 μg m(-3)), 115.9 μg m(-3) (44.2-345.4 μg m(-3)), and 85.1 μg m(-3) (24.3-232.8 μg m(-3)), respectively. The PAH concentrations in terms of PM2.5 in Beijing, Jinan, and Shanghai ranged from 23.2 to 819.8 ng m(-3), 25.7 to 727.1 ng m(-3), and 8.5 to 133.9 ng m(-3), respectively. PAH concentrations were found to be positively correlated with PM2.5 concentration in Beijing and Shanghai. The compositions of PAHs in PM2.5 in Beijing and Jinan were almost the same: 11% low ring, 80-82% middle ring, and 7-9% high ring. However, Shanghai had a different composition. Source apportionment indicated that the incomplete combustion of coal and diesel and gasoline emissions were the main sources of PAHs in PM2.5 in all three cities, whereas Shanghai had a greater contribution from liquid fossil fuels. The values for the health risk assessment estimated by the benzo[a]pyrene equivalent concentration in Beijing and Jinan were 2.39 × 10(-6) and 2.57 × 10(-6), respectively, thus both exceeding the 1 × 10(-6) limit (USEPA) considered likely to pose an inhalation cancer risk to people. Shanghai, however, had a risk estimate of 5.05 × 10(-7), which is still in a safe range. This study is the first to simultaneously monitor the PAHs in PM2.5 in three cities in Eastern China and may point to a long-range transportation of PM2.5-PAHs from Beijing to Jinan and partially to Shanghai. PMID:27148926

  14. Bioremediation of PAH contaminated soil samples

    SciTech Connect

    Joshi, M.M.; Lee, S.

    1994-12-31

    Soils contaminated with polynuclear aromatic hydrocarbons (PAHs) pose a hazard to life. The remediation of such sites can be done using physical, chemical, and biological treatment methods or a combination of them. It is of interest to study the decontamination of soil using bioremediation. The experiments were conducted using Acinetobacter (ATCC 31012) at room temperature without pH or temperature control. In the first series of experiments, contaminated soil samples obtained from Alberta Research Council were analyzed to determine the toxic contaminant and their composition in the soil. These samples were then treated using aerobic fermentation and removal efficiency for each contaminant was determined. In the second series of experiments, a single contaminant was used to prepare a synthetic soil sample. This sample of known composition was then treated using aerobic fermentation in continuously stirred flasks. In one set of flasks, contaminant was the only carbon source and in the other set, starch was an additional carbon source. In the third series of experiments, the synthetic contaminated soil sample was treated in continuously stirred flasks in the first set and in fixed bed in the second set and the removal efficiencies were compared. The removal efficiencies obtained indicated the extent of biodegradation for various contaminants, the effect of additional carbon source, and performance in fixed bed without external aeration.

  15. Polycyclic aromatic hydrocarbons in Danish leafy crops. Part I: PAH in kale and beets relate to point sources of PAH. Part II: a survey of PAH in commercial grown fresh and deep-frozen kale

    SciTech Connect

    Vahl, M.; Beck, J.; Stoebet, M.

    1982-01-01

    Part I discusses the investigation of Polycyclic Aromatic Hydrocarbons (PAH) has been to demonstrate the possible pollution of leafy vegetables from expected PAH-emmissions, and to compare with similar investigations in Scandinavia. Part II is a survey has been to establish levels of PAH to which consumers are normally exposed from intake of fruits and above ground parts of vegetables.

  16. 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

  17. Gas/particle partitioning of n-alkanes, PAHs and oxygenated PAHs in urban Denver

    NASA Astrophysics Data System (ADS)

    Xie, Mingjie; Hannigan, Michael P.; Barsanti, Kelley C.

    2014-10-01

    In this study, a medium volume sampler equipped with quartz fiber filters (QFFs) and a polyurethane foam (PUF)/XAD-4/PUF sandwich (PXP) was used to collect semi-volatile organic compounds (SVOCs) in both gaseous and particle (PM2.5) phases. A backup QFF (bQFF) was used to evaluate possible sampling artifact of particulate organics due to vapor-phase adsorption. A series of n-alkanes (molecular weight: 170-562) and PAHs (128-300), and two oxy-PAHs (acenaphthenone, 168; fluorenone, 180) were measured. Breakthrough experiments demonstrated that the PXP could collect all gas-phase target compounds with high efficiency, even the low molecular weight (MW) species (e.g., naphthalene). Comparing species concentrations across different sampling matrices encountered at the Denver, Colorado field site, the light n-alkanes (MW < 282) and PAHs (MW < 192) were mostly distributed into the gas phase; while those heavy n-alkanes (MW > 324) and PAHs (MW > 202) were primarily in the particle phase (Average temperature, 12.5 ± 10.1 °C). Log values of measured gas/particle (G/P) partitioning coefficients (Kmp,OM) of selected SVOCs (docosane, tricosane, fluoranthene, pyrene, acenaphthenone and fluorenone) were linearly regressed to those of theoretically-based partitioning coefficients (Ktp,OM) for comparison. Prior to Kmp,OM calculation, the gas- and particle-phase concentrations of SVOCs were corrected following two different approaches based on bQFF measurements. The first approach assumed that the bQFF associated SVOCs were from the adsorption of gaseous SVOCs (positive artifact); the second approach assumed equal contributions from positive and negative (organics evaporated from top QFF and adsorbed by bQFF) artifacts. Under both corrections, significant correlations (p < 0.05) were observed between log Kmp,OM and log Ktp,OM for the six selected SVOCs, suggesting that the predicted G/P partitioning can reasonably capture the measured G/P partitioning behavior. The large

  18. White upconversion luminescence nanocrystals for the simultaneous and selective detection of 2,4,6-trinitrotoluene and 2,4,6-trinitrophenol.

    PubMed

    Ma, Yingxin; Huang, Sheng; Deng, Mingliang; Wang, Leyu

    2014-05-28

    A highly water stable and strong upconversion (UC) luminescence NaYF4@PSI-NH nanosensor for the simultaneous and selective detection of 2,4,6-trinitrotoluene (TNT) and 2,4,6-trinitrophenol (TNP) was successfully developed. Via the 980 nm near-infrared (NIR) irradiation, these nanosensors emit strong white UC luminescence with five typical emission peaks centered at 363, 455, 475, 546, and 654 nm. The UC emission at both 363 and 546 nm was quenched by the addition of TNT; however, the ratio of luminescence intensity at 363 nm to 546 nm (I363/I546) had no change with the increase of TNT concentration. Meanwhile, only violet UC emission at 363 nm was dramatically quenched via the addition of TNP, and the I363/I546 ratio is negatively proportional to the TNP concentration in the range of 0.01-4.5 μg/mL of TNP. On the other hand, the green UC emission intensity at 546 nm is in negative proportion to the concentration of TNT. Moreover, cyclohexane, toluene, and other nitroaromatics (such as 2,4-dinitrotoluene (DNT) and nitrobenzene (NB)) have no influence on the detection. Therefore, we developed a facile method for the simultaneous and selective detection of TNT and TNP in the mixture solution of nitroaromatics independent of complicated instruments and sample pretreatment. PMID:24734988

  19. Theoretical design of energetic nitrogen-rich derivatives of 1,7-diamino-1,7-dinitrimino-2,4,6-trinitro-2,4,6-triazaheptane.

    PubMed

    Wu, Qiong; Zhu, Weihua; Xiao, Heming

    2013-08-01

    The heats of formation (HOFs), energetic properties, and thermal stability of a series of 1,7-diamino-1,7-dinitrimino-2,4,6-trinitro-2,4,6-triazaheptane derivatives with different substituents, different numbers of substituents, and different original chains are found by using the DFT-B3LYP method. The results show that -NO2 or -NH2 is an effective substituent for increasing the gas-phase HOFs of the title compounds, especially -NO2 group. As the numbers of substitutents increase, their HOFs enhance obviously. Increasing the length of original chain is helpful for improving their HOFs. The substitution of -NO2 is useful for enhancing their detonation performances and the effects of the length of original chains on detonation properties are coupled with those of the substituents. An analysis of the BDE of the weakest bonds indicates that the substitution of the -NH2 groups and replacing the -NO2 groups of N-NO2 by the -NH2 groups are favorable for improving their thermal stability, while the substitution of -NO2 and increasing the length of original chain decrease their thermal stability. Considering the detonation performance and thermal stability, seven compounds may be considered as the potential candidates of high energy density compounds. PMID:23559097

  20. Vicarious nucleophilic substitution to prepare 1,3-diamino-2,4,6-trinitrobenzene or 1,3,5-triamino-2,4,6-trinitrobenzene

    DOEpatents

    Mitchell, A.R.; Pagoria, P.F.; Schmidt, R.D.

    1996-10-29

    The present invention relates to a process to produce 1,3-diamino-2,4,6-trinitrobenzene (DATB) or 1,3,5-triamino-2,4,6,trinitrobenzene (TATB) by: (a) reacting at ambient pressure and a temperature of between about 0 and 50 C for between about 0.1 and 24 hr, a trinitroaromatic compound of the structure shown within where X, Y, and Z are each independently selected from --H, or --NH{sub 2}, with the proviso that at least 1 or 2 of X, Y, and Z are hydrogen, with an amount effective to produce DATB or TATB, or 1,1,1-trialkylhydrazinium halide wherein alkyl is selected from methyl, ethyl, propyl or butyl and halide is selected from chloride, bromide or iodide, in the presence of a strong base selected from sodium butoxide, potassium butoxide, potassium propoxide, sodium propoxide, sodium ethoxide, potassium ethoxide, sodium methoxide, potassium methoxide, and combinations thereof; in a solvent selected from the group consisting of methanol, ethanol, propanol, butanol, dimethylsulfoxide, N-methylpyrrolidone, hexamethylphosphoramide, dimethylformide, dimethylacetamide and mixtures thereof, provided that when alcohols are present primarily DATB and picramide is formed; and (b) isolating the DATB or TATB produced. DATB and TATB are useful specialty explosives. TATB is also used for the preparation of benzenehexamine, a starting material for the synthesis of novel materials (optical imaging devices, liquid crystals, ferromagnetic compounds).

  1. Vicarious nucleophilic substitution to prepare 1,3-diamino-2,4,6-trinitrobenzene or 1,3,5-triamino-2,4,6-trinitrobenzene

    DOEpatents

    Mitchell, Alexander R.; Pagoria, Philip F.; Schmidt, Robert D.

    1996-01-01

    The present invention relates to a process to produce 1,3-diamino-2,4,6-trinitrobenzene (DATB) or 1,3,5-triamino-2,4,6,-trinitrobenzene (TATB) by: (a) reacting at ambient pressure and a temperature of between about 0.degree. and 50.degree. C. for between about 0.1 and 24 hr, a trinitroaromatic compound of structure V: ##STR1## wherein X, Y, and Z are each independently selected from --H, or --NH.sub.2, with the proviso that at least 1 or 2 of X, Y, and Z are hydrogen, with an amount effective to produce DATB or TATB of 1,1,1-trialkylhydrazinium halide wherein alkyl is selected from methyl, ethyl, propyl or butyl and halide is selected from chloride, bromide or iodide. in the presence of a strong base selected from sodium butoxide, potassium butoxide, potassium propoxide, sodium propoxide, sodium ethoxide, potassium ethoxide, sodium methoxide, potassium methoxide, and combinations thereof; in a solvent selected from the group consisting of methanol, ethanol, propanol, butanol, dimethylsulphoxide, N-methylpyrrolidone, hexamethylphosphoramide, dimethylformide, dimethylacetamide and mixtures thereof, provided that when alcohols are present primarily DATB and picramide is formed; and (b) isolating the DATB or TATB produced. DATB and TATB are useful specialty explosives. TATB is also used for the preparation of benzenehexamine, a starting material for the synthesis of novel materials (optical imaging devices, liquid crystals, ferromagnetic compounds).

  2. Inositol 1,3,4,6-tetrakisphosphate mobilizes calcium in Xenopus oocytes with high potency.

    PubMed Central

    Ivorra, I; Gigg, R; Irvine, R F; Parker, I

    1991-01-01

    Injection of Ins(1,3,4,6)P4 into Xenopus oocytes evoked Ca2(+)-dependent membrane currents with a potency 5-10 times less than Ins(1,4,5)P3, whereas Ins(1,3,4)P3 and Ins(1,3,4,5,6)P5 were almost ineffective. Responses to Ins(1,3,4,6)P4 arose through liberation of intracellular Ca2+ and through entry of extracellular Ca2+. These results, together with the observation that Ins(1,3,4,6)P4 facilitated responses to Ins(1,4,5)P3, suggests that both of these compounds may act on the same intracellular receptors. PMID:1991032

  3. Photolysis degradation of polyaromatic hydrocarbons (PAHs) on surface sandy soil.

    PubMed

    El-Saeid, Mohamed H; Al-Turki, Ali M; Nadeem, Mahmoud E A; Hassanin, Ashraf S; Al-Wabel, Mohamed I

    2015-07-01

    Polycyclic aromatic hydrocarbons (PAHs) are potent environmental pollutants, and some of them have been identified as carcinogenic and mutagenic. To advance the knowledge of the environmental fate of PAHs, we systematically investigated the influence of different UV wavelengths irradiation on photolysis of PAHs on sandy soil under tow wavelengths (254 and 306 nm) UV irradiation for six PAHs. In addition, kinetic model and influence of several parameters on PAHs photolysis have been studied. The results obtained indicated that UV radiation with a wavelength of 306 nm was more efficient in the photolysis of the polycyclic aromatic hydrocarbons. Our results showed that fluoranthene (Flt) was the fastest in decomposition, has the greatest value for the coefficient of photolysis (7.4 × 10(-3) h(-1)), and has less half-life, reaching 94 h when using a wavelength of 254 nm. The results indicated that the pyrene (Pyr) was more resistant to photolysis in comparison with indeno(1,2,3-cd) pyrene (IP) and fluoranthene (Flt). The results indicate that photolysis is a successful way to remediate the six studied PAHs compounds. PMID:25586619

  4. Atmospheric PAHs in North China: Spatial distribution and sources.

    PubMed

    Zhang, Yanjun; Lin, Yan; Cai, Jing; Liu, Yue; Hong, Linan; Qin, Momei; Zhao, Yifan; Ma, Jin; Wang, Xuesong; Zhu, Tong; Qiu, Xinghua; Zheng, Mei

    2016-09-15

    Polycyclic aromatic hydrocarbons (PAHs), formed through incomplete combustion process, have adverse health effects. To investigate spatial distribution and sources of PAHs in North China, PAHs with passive sampling in 90 gridded sites during June to September in 2011 were analyzed. The average concentration of the sum of fifteen PAHs in North China is 220±14ng/m(3), with the highest in Shanxi, followed by Shandong and Hebei, and then the Beijing-Tianjin area. Major sources of PAHs are identified for each region of North China, coke process for Shanxi, biomass burning for Hebei and Shandong, and coal combustion for Beijing-Tianjin area, respectively. Emission inventory is combined with back trajectory analysis to study the influence of emissions from surrounding areas at receptor sites. Shanxi and Beijing-Tianjin areas are more influenced by sources nearby while regional sources have more impact on Hebei and Shandong areas. Results from this study suggest the areas where local emission should be the major target for control and areas where both local and regional sources should be considered for PAH abatement in North China. PMID:27241206

  5. Steps Toward Identifying PAHs: A Child's Garden of Recent Results

    NASA Technical Reports Server (NTRS)

    Hudgins, Douglas M.

    2005-01-01

    Based on over two decades of experimental, observational and theoretical studies by scientists around the world. It is now widely accepted that the composite emission of mixtures of vibrationally-excited PAHs and PAH ions can accommodate the general pattern of band positions, intensities, and profiles observed in the discreet IR emission features of carbon-rich interstellar dust, as well as the variations in those characteristics. These variations provide insight into the detailed nature of the emitting PAH population and reflect conditions within the emitting regions giving the population enormous potential as probes of astrophysical environments. Moreover, the ubiquity and abundance of this material has impacts that extend well beyond the IR. In this presentation we will examine recent, combined experimental, theoretical, and observational studies that indicate that nitrogen-substituted PAHs represent an important component of the interstellar dust population, and we will go on to explore some of the ramifications of this result. We will also explore the results of recent experimental studies of the strong, low-lying electronic transitions of ionized PAH ions in the Near-IR (0.7 - 2.5 microns) and explore the role that these transitions might play in pumping the PAH IR emission in regions of low-excitation.

  6. Hydrogenation of PAH molecules through interaction with hydrogenated carbonaceous grains.

    PubMed

    Thrower, John D; Friis, Emil E; Skov, Anders L; Jørgensen, Bjarke; Hornekær, Liv

    2014-02-28

    Carbonaceous materials contribute to a significant proportion of the interstellar dust inventory. Reactions on such grain surfaces are thought to play important roles in interstellar chemical networks. Of particular importance are reactions involving hydrogen atoms, and pathways to the formation of the most abundant molecular species, H2. Polycyclic aromatic hydrocarbons (PAHs) are an additional carbon reservoir, accounting for around 10% of the galactic carbon budget. Using thermal desorption and mass spectrometric techniques, we have investigated the interaction between PAH molecules and carbonaceous grain surfaces. We demonstrate that deuterium atoms adsorbed on graphite can react with adsorbed PAH molecules, forming superhydrogenated PAH species. Furthermore, by considering the number of D-atoms remaining bound to the graphite surface and the additional D-atoms in the observed superhydrogenated species, we see evidence for a significant release of deuterium from the graphite surface. We suggest that further reactive processes may be responsible for part of this deuterium loss, indicating that PAHs adsorbed on hydrogenated carbonaceous grains in warm interstellar environments may serve as a route to release H2 as well as forming superhydrogenated PAH species. PMID:24270708

  7. Polycyclic aromatic hydrocarbons (PAHs) in ambient aerosols from Beijing: characterization of low volatile PAHs by positive-ion atmospheric pressure photoionization (APPI) coupled with Fourier transform ion cyclotron resonance.

    PubMed

    Jiang, Bin; Liang, Yongmei; Xu, Chunming; Zhang, Jingyi; Hu, Miao; Shi, Quan

    2014-05-01

    Aromatic fractions derived from aerosol samples were characterized by gas chromatography and mass spectrometry (GC-MS), high temperature simulated distillation (SIMDIS), and positive-ion atmospheric pressure photoionization (APPI) Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS), respectively. It was found that about 27 wt % compounds in aromatic fractions could not be eluted from a GC column and some large molecule PAHs were neglected in GC-MS analysis. APPI FT-ICR MS was proven to be a powerful approach for characterizing the molecular composition of aromatics, especially for the large molecular species. An aromatic sample from Beijing urban aerosol was successfully characterized by APPI FT-ICR MS. Results showed that most abundant aromatic compounds in PM2.5 (particles with aerodynamic diameter ≤ 2.5 μm) were highly condensed hydrocarbons with 4-8 aromatic rings and their homologues with very short alkyl chains. Furthermore, heteroatom-containing hydrocarbons were found as the significant components of the aromatic fractions: O1, O2, N1, and S1 class species with 10-28 DBEs (double bond equivalents) and 14-38 carbon numbers were identified by APPI FT-ICR MS. The heteroatom PAHs had similar DBEs and carbon number distribution as regular PAHs. PMID:24702199

  8. Optimizing Thomson's jumping ring

    NASA Astrophysics Data System (ADS)

    Tjossem, Paul J. H.; Brost, Elizabeth C.

    2011-04-01

    The height to which rings will jump in a Thomson jumping ring apparatus is the central question posed by this popular lecture demonstration. We develop a simple time-averaged inductive-phase-lag model for the dependence of the jump height on the ring material, its mass, and temperature and apply it to measurements of the jump height for a set of rings made by slicing copper and aluminum alloy pipe into varying lengths. The data confirm a peak jump height that grows, narrows, and shifts to smaller optimal mass when the rings are cooled to 77 K. The model explains the ratio of the cooled/warm jump heights for a given ring, the reduction in optimal mass as the ring is cooled, and the shape of the mass resonance. The ring that jumps the highest is found to have a characteristic resistance equal to the inductive reactance of the set of rings.

  9. 1,5,2,4,6,8-Dithiatetrazocine. Synthesis, computation, crystallography and voltammetry of the parent heterocycle.

    PubMed

    Moock, Klaus H; Wong, Ken M; Boeré, René T

    2011-11-21

    The prototypal 1,5,2,4,6,8-dithiatetrazocine has been synthesized for the first time by two routes: reaction of 1,2,3,5-dithiadiazolium chloride with N,N,N'-tris(trimethylsilyl)formamidine in acetonitrile and reaction of 1,2,3,5-dithiadiazolyl radical with dioxygen in solution. Yields are low but single crystals could be obtained for an X-ray crystal structure determination which shows it to have the planar delocalized structure predicted by B3LYP/6-311+G(2d,p) hybrid DFT calculations. The crystal structure is strongly reminiscent of that of benzene in the same Pbca space group. Aromaticity is demonstrated by a (1)H NMR chemical shift of +9.70 ppm indicative of diamagnetic ring shielding and an intense low-energy optical absorption with λ(max) = 349 nm (MeOH). The voltammetric behaviour of the title compound is compared with that of 1,3λ(4)δ(2),5,2,4-trithiadiazepine; both resist electrochemical oxidation and reduction over a wide potential range as is typical for aromatic heterocycles. PMID:21956480

  10. Polycyclic aromatic hydrocarbons (PAHs) and their derivatives (oxygenated-PAHs, nitrated-PAHs and azaarenes) in size-fractionated particles emitted in an urban road tunnel

    NASA Astrophysics Data System (ADS)

    Alves, C. A.; Vicente, A. M. P.; Gomes, J.; Nunes, T.; Duarte, M.; Bandowe, B. A. M.

    2016-11-01

    A sampling campaign of size segregated particulate matter (PM0.5, PM0.5-1, PM1-2.5 and PM2.5-10) was carried out at two sites, one in a road tunnel (Braga, Portugal) and another at an urban background location in the neighbourhood. Particle-bound polycyclic aromatic compounds were extracted with organic solvents and analysed by gas chromatography-mass spectrometry. Twenty six parent and alkyl-polycyclic aromatic hydrocarbons (PAHs), 4 azaarenes (AZAs), 15 nitrated and 15 oxygenated derivatives (NPAHs and OPAHs) were analysed. On average, submicron particles (PM1) in the tunnel comprised 93, 91, 96 and 71% of the total PAHs, OPAHs, NPAHs and AZAs mass in PM10, respectively. Tunnel to outdoor PAH concentration ratios between 10 and 14 reveal the strong contribution of fresh exhaust emissions to the PM loads. The dominant PAHs in the tunnel were pyrene, retene and benzo[ghi]perylene, accounting for 20, 17 and 8% of the total PAH levels in PM10, respectively. Isomer ratios indicated the importance of unburnt fuel as a significant PAH source. The only NPAH consistently present in all samples was 5-nitroacenaphthene. Indanone and 1,8-naphthalic anhydride were the most abundant OPAHs, accounting for 25 and 17% of the total concentrations of this organic class, respectively. Other abundant OPAHs were 1,4-naphthoquinone, 9-fluorenone, 1,2-acenaphthylenequinone and 7H-benz[de]anthracene-7-one. Individual emission factors (μg veh- 1 km- 1) were estimated and compared with those obtained in other tunnel studies.

  11. Chiral, triformylphenol-derived salen-type [4 + 6] organic cages.

    PubMed

    Petryk, M; Szymkowiak, J; Gierczyk, B; Spólnik, G; Popenda, Ł; Janiak, A; Kwit, M

    2016-08-21

    A one-pot synthesis of chiral [4 + 6] tetrahedral cage compounds containing a salen fragment on each face is presented. The formation of the [4 + 6] products remains in contrast to the reaction of 1,3,5-triformylphloroglucinol with chiral diamines where [2 + 3] keto-enamine pseudocyclophanes are formed exclusively. The presence of OH groups determines the structural and spectroscopic properties of these cage compounds while a change in the reaction conditions facilitates the isolation of the microcrystalline products of the specific surface area varying from 5 to 578 m(2) g(-1). PMID:27420910

  12. Toxicological characterization of 2,4,6-trinitrotoluene, its transformation products, and two nitramine explosives.

    PubMed

    Neuwoehner, Judith; Schofer, Andrea; Erlenkaemper, Bibiane; Steinbach, Klaus; Hund-Rinke, T Kerstin; Eisentraeger, Adolf

    2007-06-01

    The soil and groundwater of former ordnance plants and their dumping sites have often been highly contaminated with the explosive 2,4,6-trinitrotoluene (2,4,6-TNT) leading to a potential hazard for humans and the environment. Further hazards can arise from metabolites of transformation, by-products of the manufacturing process, or incomplete combustion. This work examines the toxicity of polar nitro compounds relative to their parent compound 2,4,6-TNT using four different ecotoxicological bioassays (algae growth inhibition test, daphnids immobilization test, luminescence inhibition test, and cell growth inhibition test), three genotoxicological assays (umu test, NM2009 test, and SOS Chromotest), and the Ames fluctuation test for detection of mutagenicity. For this study, substances typical for certain steps of degradation/transformation of 2,4,6-TNT were chosen for investigation. This work determines that the parent compounds 2,4,6-TNT and 1,3,5-trinitrobenzene are the most toxic substances followed by 3,5-dinitrophenol, 3,5-dinitroaniline and 4-amino-2-nitrotoluene. Less toxic are the direct degradation products of 2,4,6-TNT like 2,4-dinitrotoluene, 2,6-dinitrotoluene, 2-amino-4,6-dinitrotoluene, and 4-amino-2,6-dinitrotoluene. A weak toxic potential was observed for 2,4,6-trinitrobenzoic acid, 2,4-diamino-6-nitrotoluene, 2,4-dinitrotoluene-5-sulfonic acid, and 2,6-diamino-4-nitrotoluene. Octahydro-l,3,5,7-tetranitro-l,3,5,7-tetrazocine and hexahydro-1,3,5-trinitro-l,3,5-triazine show no hint of acute toxicity. Based on the results of this study, we recommend expanding future monitoring programs of not only the parent substances but also potential metabolites based on conditions at the contaminated sites and to use bioassays as tools for estimating the toxicological potential directly by testing environmental samples. Site-specific protocols should be developed. If hazardous substances are found in relevant concentrations, action should be taken to prevent

  13. Toward the Oxidation of the Phenyl Radical and Prevention of PAH Formation in Combustion Systems.

    PubMed

    Parker, Dorian S N; Kaiser, Ralf I; Troy, Tyler P; Kostko, Oleg; Ahmed, Musahid; Mebel, Alexander M

    2015-07-16

    The reaction of the phenyl radical (C6H5) with molecular oxygen (O2) plays a central role in the degradation of poly- and monocyclic aromatic radicals in combustion systems which would otherwise react with fuel components to form polycyclic aromatic hydrocarbons (PAHs) and eventually soot. Despite intense theoretical and experimental scrutiny over half a century, the overall reaction channels have not all been experimentally identified. Tunable vacuum ultraviolet photoionization in conjunction with a combustion simulating chemical reactor uniquely provides the complete isomer specific product spectrum and branching ratios of this prototype reaction. In the reaction of phenyl radicals and molecular oxygen at 873 K and 1003 K, ortho-benzoquinone (o-C6H4O2), the phenoxy radical (C6H5O), and cyclopentadienyl radical (C5H5) were identified as primary products formed through emission of atomic hydrogen, atomic oxygen and carbon dioxide. Furan (C4H4O), acrolein (C3H4O), and ketene (C2H2O) were also identified as primary products formed through ring opening and fragmentation of the 7-membered ring 2-oxepinoxy radical. Secondary reaction products para-benzoquinone (p-C6H4O2), phenol (C6H5OH), cyclopentadiene (C5H6), 2,4-cyclopentadienone (C5H4O), vinylacetylene (C4H4), and acetylene (C2H2) were also identified. The pyranyl radical (C5H5O) was not detected; however, electronic structure calculations show that it is formed and isomerizes to 2,4-cyclopentadienone through atomic hydrogen emission. In combustion systems, barrierless phenyl-type radical oxidation reactions could even degrade more complex aromatic radicals. An understanding of these elementary processes is expected to lead to a better understanding toward the elimination of carcinogenic, mutagenic, and environmentally hazardous byproducts of combustion systems such as PAHs. PMID:25354358

  14. The effects of PAHs and N-PAHs on retinoid signaling and Oct-4 expression in vitro.

    PubMed

    Beníšek, Martin; Kubincová, Petra; Bláha, Luděk; Hilscherová, Klára

    2011-02-01

    Polycyclic aromatic hydrocarbons (PAHs) and their N-heterocyclic analogs (N-PAHs) are important environmental contaminants with negative effects in living organisms, including teratogenicity and embryotoxicity. Though most studies linked their embryotoxicity with aryl hydrocarbon receptor (AhR) and cytochrome P450 activation, the exact mechanism is not known. Other mechanisms such as disruption of retinoid signaling were recently suggested to be of importance. This study investigated PAHs and N-PAHs interference with retinoid signaling in vitro by modulating all-trans retinoic acid (ATRA) mediated response in a reporter gene assay using P19/A15 cell line. Further, effects on pluripotency and differentiation processes were evaluated by measuring octamer-4 (Oct-4), an important pluripotency marker and master differentiation factor. Two of the studied compounds, benz[a]anthracene and benz[c]acridine significantly up-regulated ATRA-mediated response in the co-exposure with a range of ATRA concentrations. Another structural N-PAH variant, 1,7-phenanthroline, downregulated ATRA-mediated response at most of tested ATRA concentrations and exposure times. Interesting concentration-dependent biphasic effects (i.e. downregulation with subsequent up-regulation to control levels) were observed at co-exposures of ATRA and parent PAH phenanthrene. Non significant Oct-4 modulation in co-exposure with ATRA was observed at compounds, which potentiated ATRA-mediated effects in the reporter gene assay. On the other hand, 1,7-phenanthroline and phenanthrene significantly suppressed Oct-4 levels in higher tested concentrations. Our results further extend the knowledge of PAH and N-PAH in vitro effects and indicate that these environmental toxicants may have influence on differentiation process and embryonic development by interfering with ATRA signaling and by modulating levels of Oct-4. PMID:21111795

  15. Hemodynamics in pulmonary arterial hypertension (PAH): do they explain long-term clinical outcomes with PAH-specific therapy?

    PubMed Central

    2010-01-01

    Background Pulmonary arterial hypertension (PAH) has witnessed dramatic treatment advances over the past decade. However, with the exception of epoprostenol, data from short-term randomized controlled trials (RCTs) have not shown a benefit of these drugs on survival. There remains a need to differentiate between available therapies and current endpoint responses which in turn, could be used to guide treatment selection and provide long-term prognostic information for patients. Methods We performed a systematic literature search of MEDLINE and EMBASE databases for RCTs of PAH-specific therapy published between January 1980 and May 2009. Articles were selected if they contained a placebo comparator and described hemodynamic changes from baseline. We applied the weighted mean change in hemodynamic variables to the equation developed by the National Institutes of Health (NIH) Registry to estimate long-term survival with each therapy. Results Ten RCTs involving 1,635 patients met the inclusion criteria. Suitable hemodynamic data were identified for bosentan, sitaxentan, sildenafil, epoprostenol, beraprost and treprostinil. 77.6% of patients were female and the mean (SD) age was 46.5 ± 4.9 years. 55.5% of patients had idiopathic PAH (iPAH), 23.9% PAH related to connective tissue disease, and 18.2% PAH related to congenital heart disease. Based on the effects observed in short-term trials and, relative to placebo, all analyzed therapies improved survival. The estimated 1-year survival was 78.4%, 77.8%, 76.1%, 75.8%, 75.2%, and 74.1% for epoprostenol, bosentan, treprostinil, sitaxentan, sildenafil, and beraprost, respectively. These estimates are considerably lower than the 1-year observed survival reported in several open-label and registry studies with PAH-specific therapies: 88% - 97%. Conclusion When applied to the NIH Registry equation, hemodynamic changes from baseline appear to underestimate the survival benefits observed with long-term PAH therapy. PMID:20170553

  16. Jupiter's Main Ring/Ring Halo

    NASA Technical Reports Server (NTRS)

    1997-01-01

    A mosaic of four images taken through the clear filter (610 nanometers) of the solid state imaging (CCD) system aboard NASA's Galileo spacecraft on November 8, 1996, at a resolution of approximately 46 kilometers (28.5 miles) per picture element (pixel) along Jupiter's rings. Because the spacecraft was only about 0.5 degrees above the ring plane, the image is highly foreshortened in the vertical direction. The images were obtained when Galileo was in Jupiter's shadow, peering back toward the Sun; the ring was approximately 2.3 million kilometers (1.4 million miles) away. The arc on the far right of the image is produced when sunlight is scattered by small particles comprising Jupiter's upper atmospheric haze. The ring also efficiently scatters light, indicating that much of its brightness is due to particles that are microns or less in diameter. Such small particles are believed to have human-scale lifetimes, i.e., very brief compared to the solar system's age.

    Jupiter's ring system is composed of three parts - - a flat main ring, a lenticular halo interior to the main ring, and the gossamer ring, outside the main ring. The near and far arms of Jupiter's main ring extend horizontally across the mosaic, joining together at the ring's ansa, on the figure's far left side. The near arm of the ring appears to be abruptly truncated close to the planet, at the point where it passes into Jupiter's shadow. Some radial structure is barely visible across the ring's ansa (top image). A faint mist of particles can be seen above and below the main rings. This vertically extended 'halo' is unusual in planetary rings, and is probably caused by electromagnetic forces pushing the smallest grains out of the ring plane. Because of shadowing, the halo is not visible close to Jupiter in the lower right part of the mosaic. To accentuate faint features in the bottom image of the ring halo, different brightnesses are shown through color. Brightest features are white or yellow and the

  17. On semi ring bornologies

    NASA Astrophysics Data System (ADS)

    Imran, A. N.; Rakhimov, I. S.; Husain, Sh. K. Said

    2016-06-01

    Our main focus in this work is to introduce new structure bornological semi rings. This generalizes the theory of algebraic semi rings from the algebraic setting to the framework of bornological sets. We give basic properties for this new structure. As well as, We study the fundamental construction of bornological semi ring as product, inductive limits and projective limits and their extensions on bornological semi ring. Additionally, we introduce the category of bornological semi rings and study product and pullback (fiber product) in the category of bornological semi rings.

  18. PAH composition of Water Based Drilling Mud and drill cuttings in the offshore region, east coast of India.

    PubMed

    Jagwani, Devaanshi; Kulkarni, Atul; Shukla, Parth; Ramteke, Dilip S; Juneja, Harjeet D

    2011-11-01

    As a consequence of offshore drilling, used Water Based Drilling Muds (WBMs) are typically disposed off, by discharging into the sea; such a disposal does not fully eliminate the environmental hazards. Hence, in this study, 2, 3, 4 and 5 ringed polycyclic aromatic hydrocarbons (PAHs i.e. naphthalene, fluorene, phenanthrene, fluoranthene, chrysene and benzo (a) pyrene) were determined from the WBMs and associated drill cuttings obtained from varying depths(viz. 150, 300 and 600 m) from three offshore wells present in East coast of India. In both WBMs and drill cuttings, concentration of naphthalene was maximum i.e. 81.59 ± 2.73 and 39.87 ± 2.40 mg/kg respectively, while benzo (a) pyrene was minimum i.e. 0.19 ± 0.07 and 0.12 ± 0.03 mg/kg respectively. The WBMs contained significantly (p < 0.05) higher PAH concentration than drill cuttings. The individual PAH concentration significantly (p < 0.01) increased with increasing depth in each well. PMID:21691860

  19. N-(2-{[5-Bromo-2-(piperidin-1-yl)pyrimidin-4-yl]sulfan­yl}-4-meth­oxy­phen­yl)-2,4,6-trimethyl­benzene­sulfonamide

    PubMed Central

    Kumar, Mohan; Mallesha, L.; Sridhar, M. A.; Kapoor, Kamini; Gupta, Vivek K.; Kant, Rajni

    2012-01-01

    In the title compound, C25H29BrN4O3S2, the benzene rings bridged by the sulfonamide group are tilted relative to each other by 63.9 (1)° and the dihedral angle between the sulfur-bridged pyrimidine and benzene rings is 64.9 (1)°. The mol­ecular conformation is stabilized by a weak intra­molecular π–π stacking inter­action between the pyrimidine and the 2,4,6-trimethyl­benzene rings [centroid–centroid distance = 3.766 (2) Å]. The piperidine ring adopts a chair conformation. In the crystal, mol­ecules are linked into inversion dimers by pairs of N—H⋯O hydrogen bonds and these dimers are further linked by C—H⋯O hydrogen bonds into chains propagating along [010]. PMID:22969648

  20. Monoclinic structure of hydroxylpyromorphite Pb10(PO4)6(OH)2 - hydroxylmimetite Pb10(AsO4)6(OH)2 solid solution series

    NASA Astrophysics Data System (ADS)

    Giera, Alicja; Manecki, Maciej; Borkiewicz, Olaf; Zelek, Sylwia; Rakovan, John; Bajda, Tomasz; Marchlewski, Tomasz

    2016-04-01

    Seven samples of hydroxyl analogues of pyromorphite-mimetite solid solutions series were synthesized from aqueous solutions at 80° C in a computer-controlled chemistate: 200 mL aqueous solutions of 0.05M Pb(NO3)2 and 0.03M KH2AsO4 and/or KH2PO4 were dosed with a 0.25 mL/min rate to a glass beaker, which initially contained 100 mL of distilled water. Constant pH of 8 was maintained using 2M KOH. The syntheses yielded homogeneous fine-grained white precipitates composition of which was close to theoretical Pb10[(PO4)6‑x(AsO4)x](OH)2, where x = 0, 1, 2, 3, 4, 5, 6. High-resolution powder X-ray diffraction data were obtained in transmission geometry at the beamline 11-BM at the Advanced Photon Source (Argonne National Laboratory in Illinois, USA). The structure Rietveld refinements based on starting parameters of either hexagonal hydroxylpyromorphite or monoclinic mimetite-M were performed using GSAS+EXPGUI software. Apatite usually crystallizes in the hexagonal crystal system with the space group P63/m. For the first time, however, the lowering of the hexagonal to monoclinic crystal symmetry was observed in the hydroxyl variety of pyromorphite-mimetite solid solution series. This is indicated by better fitting of the modeled monoclinic structure to the experimental data. The same is not the case for analogous calcium hydroxylapatite series Ca5(PO4)3OH - Ca5(AsO4)3OH (Lee et al. 2009). Systematical linear increase of unit cell parameters is observed with As substitution from a=9.88, b=19.75, and c=7.43 for Pb10(PO4)6(OH)2 to a=10.23, b=20.32, and c=7.51 for Pb10(AsO4)6(OH)2. A strong pseudohexagonal character (γ ≈ 120° and b ≈ 2a) of the analyzed monoclinic phases was established. This work is partially funded by AGH research grant no 11.11.140.319 and partially by Polish NCN grant No 2011/01/M/ST10/06999. Lee Y.J., Stephens P.W., Tang Y., Li W., Philips B.L., Parise J.B., Reeder R.J., 2009. Arsenate substitution in hydroxylapatite: Structural characterization

  1. Removal efficiency of vapour/particulate phase PAHs by using alternative protective respirators in PAHs exposure workers.

    PubMed

    Chen, Hsiu-Ling; Yang, Chien-Hung; Lin, Ming-Hsiu

    2012-06-15

    Due to the high heat environment in foundry industries, it is difficult for foundry workers to wear masks during their workday. Thus, how to prevent inhaling vapour or the particulate phase of polycyclic aromatic hydrocarbons (PAHs) is important for occupational hazard management. The present study assesses the characteristics of PAHs emission in foundry and plastic industries to evaluate the removal efficiencies of PAHs while workers use alternative personal protective equipment. The highest 1-hydroxypyrene (1-OHP) level was found for workers who used a cotton-fabric face mask (1.19 μg/g creatinine) and activated-carbon face mask (1.16 μg/g creatinine), compared to a lower level in workers who wore a surgical face mask (0.27 μg/g creatinine) and a N95 respirator (0.51 μg/g creatinine). The urinary 1-OHP in end-of-shift samples correlated to the airborne vapour phase Bapeq, but not for the particulate phase Bapeq in the foundry industry. This is probably because workers wore personal protective equipment that only removed the particulate phase PAH. The current study suggests that future work focus on developing an appropriate and comfortable respirator with high removal efficiency for ultrafine particulates and vapour phase PAHs simultaneously in PAH work environments. PMID:22525483

  2. Correlations between PAH bioavailability, degrading bacteria, and soil characteristics during PAH biodegradation in five diffusely contaminated dissimilar soils.

    PubMed

    Crampon, M; Bureau, F; Akpa-Vinceslas, M; Bodilis, J; Machour, N; Le Derf, F; Portet-Koltalo, F

    2014-01-01

    The natural biodegradation of seven polycyclic aromatic hydrocarbons (PAHs) by native microorganisms was studied in five soils from Normandy (France) from diffusely polluted areas, which can also pose a problem in terms of surfaces and amounts of contaminated soils. Bioavailability tests using cyclodextrin-based extractions were performed. The natural degradation of low molecular weight (LMW) PAHs was not strongly correlated to their bioavailability due to their sorption to geosorbents. Conversely, the very low degradation of high molecular weight (HMW) PAHs was partly correlated to their poor availability, due to their sorption on complexes of organic matter and kaolinites or smectites. A principal component analysis allowed us to distinguish between the respective degradation behaviors of LMW and HMW PAHs. LMW PAHs were degraded in less than 2-3 months and were strongly influenced by the relative percentage of phenanthrene-degrading bacteria over total bacteria in soils. HMW PAHs were not significantly degraded, not only because they were less bioavailable but also because of a lack of degrading microorganisms. Benzo[a]pyrene stood apart since it was partly degraded in acidic soils, probably because of a catabolic cooperation between bacteria and fungi. PMID:24671402

  3. Unlike PAHs from Exxon Valdez crude oil, PAHs from Gulf of Alaska coals are not readily bioavailable

    SciTech Connect

    Halambage Upul Deepthike; Robin Tecon; Gerry van Kooten; Jan Roelof van der Meer; Hauke Harms; Mona Wells; Jeffrey Short

    2009-08-15

    In the wake of the 1989 Exxon Valdez oil spill, spatially and temporally spill-correlated biological effects consistent with polycyclic aromatic hydrocarbon (PAH) exposure were observed. Some works have proposed that confounding sources from local source rocks, prominently coals, are the provenance of the PAHs. Representative coal deposits along the southeast Alaskan coast (Kulthieth Formation) were sampled and fully characterized chemically and geologically. The coals have variable but high total organic carbon content, technically classifying as coals and coaly shale, and highly varying PAH contents. Even for coals with high PAH content (4000 ppm total PAHs), a PAH-sensitive bacterial biosensor demonstrates nondetectable bioavailability as quantified, based on naphthalene as a test calibrant. These results are consistent with studies indicating that materials such as coals strongly diminish the bioavailability of hydrophobic organic compounds and support previous work suggesting that hydrocarbons associated with the regional background in northern Gulf of Alaska marine sediments are not appreciably bioavailable. 44 refs., 4 figs., 2 tabs.

  4. Passive samplers accurately predict PAH levels in resident crayfish.

    PubMed

    Paulik, L Blair; Smith, Brian W; Bergmann, Alan J; Sower, Greg J; Forsberg, Norman D; Teeguarden, Justin G; Anderson, Kim A

    2016-02-15

    Contamination of resident aquatic organisms is a major concern for environmental risk assessors. However, collecting organisms to estimate risk is often prohibitively time and resource-intensive. Passive sampling accurately estimates resident organism contamination, and it saves time and resources. This study used low density polyethylene (LDPE) passive water samplers to predict polycyclic aromatic hydrocarbon (PAH) levels in signal crayfish, Pacifastacus leniusculus. Resident crayfish were collected at 5 sites within and outside of the Portland Harbor Superfund Megasite (PHSM) in the Willamette River in Portland, Oregon. LDPE deployment was spatially and temporally paired with crayfish collection. Crayfish visceral and tail tissue, as well as water-deployed LDPE, were extracted and analyzed for 62 PAHs using GC-MS/MS. Freely-dissolved concentrations (Cfree) of PAHs in water were calculated from concentrations in LDPE. Carcinogenic risks were estimated for all crayfish tissues, using benzo[a]pyrene equivalent concentrations (BaPeq). ∑PAH were 5-20 times higher in viscera than in tails, and ∑BaPeq were 6-70 times higher in viscera than in tails. Eating only tail tissue of crayfish would therefore significantly reduce carcinogenic risk compared to also eating viscera. Additionally, PAH levels in crayfish were compared to levels in crayfish collected 10 years earlier. PAH levels in crayfish were higher upriver of the PHSM and unchanged within the PHSM after the 10-year period. Finally, a linear regression model predicted levels of 34 PAHs in crayfish viscera with an associated R-squared value of 0.52 (and a correlation coefficient of 0.72), using only the Cfree PAHs in water. On average, the model predicted PAH concentrations in crayfish tissue within a factor of 2.4 ± 1.8 of measured concentrations. This affirms that passive water sampling accurately estimates PAH contamination in crayfish. Furthermore, the strong predictive ability of this simple model suggests

  5. Atmospheric levels and cytotoxicity of PAHs and heavy metals in TSP and PM 2.5 at an electronic waste recycling site in southeast China

    NASA Astrophysics Data System (ADS)

    Deng, W. J.; Louie, P. K. K.; Liu, W. K.; Bi, X. H.; Fu, J. M.; Wong, M. H.

    Twenty-nine air samples of total suspended particles (TSP, particles less than 30-60 μm) and thirty samples of particles with aerodynamic diameter smaller than 2.5 μm (PM 2.5) were collected at Guiyu, an electronic waste (e-waste) recycling site in southeast China from 16 August 2004 to 17 September 2004. The results showed that mass concentrations contained in TSP and PM 2.5 were 124±44.1 and 62.12±20.5 μg m -3, respectively. The total sum of 16 USEPA priority polycyclic aromatic hydrocarbons (PAHs) associated with TSP and PM 2.5 ranged from 40.0 to 347 and 22.7 to 263 ng m -3, respectively. Five-ring and six-ring PAHs accounted for 73% of total PAHs. The average concentration of benzo(a) pyrene was 2-6 times higher than in other Asian cities. Concentrations of Cr, Cu and Zn in PM 2.5 of Guiyu were 4-33 times higher than in other Asian countries. In general, there were significant correlations between concentrations of individual contaminants in TSP with PM 2.5 (i.e. PAHs, Cd, Cr, Cu, Pb, Zn, Mn except Ni and As). The high concentrations of both PAHs and heavy metals in air of Guiyu may impose a serious environmental and health concern. Cytotoxicity of the extract of TSP and PM 2.5 of ten 24 h samples collected against human promonocytic leukemia cell line U937 (ATCC 1593.2) was determined by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide cytotoxicity assay. The results showed that under the same concentrations of extract, PM 2.5 cytotoxicity was 2-4 times higher than TSP.

  6. Distribution patterns of PAHs and trace elements in mosses Hylocomium splendens (Hedw.) B.S.G. and Pleurozium schreberi (Brid.) Mitt. from different forest communities: a case study, south-central Poland.

    PubMed

    Gałuszka, Agnieszka

    2007-04-01

    Twenty samples of the moss species Hylocomium splendens and Pleurozium schreberi were collected at 10 sites of the Holy Cross Mountains (south-central Poland) and analyzed for 16 polycyclic aromatic hydrocarbons and 33 elements. The ring sequence of PAHs in the moss samples is: 4 (92-1040 ng x g(-1))>3 and 5 (21-272 ng x g(-1))>6 (<5-131 ng x g(-1)). H. splendens accumulates PAHs more effectively than P. schreberi, and therefore the former may be regarded as a better bioindicator of PAHs. No correlation was found between concentrations of PAHs and elements. However, both H. splendens and P. schreberi shows different bioaccumulative capabilities depending on the plant communities. The mosses growing in the dry pine forest Cladonio-Pinetum reveal higher levels of Fe, Na, Sr, Ti, Cr, Mo, Ni, V and higher mean concentrations of summation operator16 PAHs, whereas those from the continental coniferous forest Querco roboris-Pinetum are highlighted by elevated levels of B, Ca, K, Mg, Mn, P, Rb and Sb and lower mean concentrations of summation operator16 PAHs. These differences seem to be brought about by a higher biodiversity of the second forest type and its higher productivity that favors more effective cycling of elements. PMID:17141296

  7. Teaching New Literacies in Grades 4-6: Resources for 21st-Century Classrooms

    ERIC Educational Resources Information Center

    Moss, Barbara, Ed.; Lapp, Diane, Ed.

    2009-01-01

    Upper-elementary students encounter a sometimes dizzying array of traditional and nontraditional texts both in and outside of the classroom. This practical handbook helps teachers in grades 4-6 harness the instructional potential of fiction, poetry, and plays; informational texts; graphic novels; digital storytelling; Web-based and multimodal…

  8. Living in Water. An Aquatic Science Curriculum for Grades 4-6. Second Edition.

    ERIC Educational Resources Information Center

    National Aquarium in Baltimore, MD. Dept. of Education.

    This document is a scientific study of water, aquatic environments and the plants and animals that live in water. It was written for grades 4-6 but many activities may also be of interest for use with older students. This curriculum covers both marine and freshwater habitats. Each of five sections addresses a question about water which is then…

  9. A Large-Scale Evaluation of the KiVa Antibullying Program: Grades 4-6

    ERIC Educational Resources Information Center

    Karna, Antti; Voeten, Marinus; Little, Todd D.; Poskiparta, Elisa; Kaljonen, Anne; Salmivalli, Christina

    2011-01-01

    This study demonstrates the effectiveness of the KiVa antibullying program using a large sample of 8,237 youth from Grades 4-6 (10-12 years). Altogether, 78 schools were randomly assigned to intervention (39 schools, 4,207 students) and control conditions (39 schools, 4,030 students). Multilevel regression analyses revealed that after 9 months of…

  10. SAGE ANALYSIS OF TRANSCRIPTOME RESPONSES IN ARABIDOPSIS ROOTS EXPOSED TO 2,4,6-TRINITROTOLUENE

    EPA Science Inventory

    Serial Analysis of Gene Expression (SAGE) was used to profile transcript levels in Arabidopsis thaliana roots and assess their responses to 2,4,6-trinitrotoluene (TNT) exposure. SAGE libraries representing control and TNT-exposed seedling root transcripts were constructed, and ea...

  11. The Greatest Educational Change America Has Ever Seen, 2001: Lesson Plans for Grades 4-6.

    ERIC Educational Resources Information Center

    United States Mint (Dept. of Treasury), Washington, DC.

    This teacher's guide on the 50 state quarters produced by the United States Mint includes six lesson plans that fit easily into the social studies curriculum for grades 4-6. The lesson plans include reproducible student work pages that coincide with each lesson; state facts and information about the 2001 state quarter designs (New York, North…

  12. The Greatest Educational Change America Has Ever Seen, 2002: Lesson Plans for Grades 4-6.

    ERIC Educational Resources Information Center

    United States Mint (Dept. of Treasury), Washington, DC.

    This teacher's guide on the 50 state quarters emitted by the United States Mint includes 6 "teacher-friendly" lesson plans that fit easily into the curriculum for grades 4-6; reproducible student worksheets that coincide with each lesson; "fun" state facts and information on the new quarter designs; and USA map template with state outlines. These…

  13. The Greatest Educational Change America Has Ever Seen. [Teaching Guide]. Grades 4-6.

    ERIC Educational Resources Information Center

    United States Mint (Dept. of Treasury), Washington, DC.

    This teaching guide for grades 4-6 focuses on the 1999-2000 United States Mint 50 State Quarters Program, which includes new quarter designs for the following states: Delaware, Pennsylvania, New Jersey, Georgia, Connecticut, Massachusetts, Maryland, South Carolina, New Hampshire, and Virginia. The guide includes six lesson plans that fit easily…

  14. Texas School Survey of Substance Use among Students: Grades 4-6, 1998.

    ERIC Educational Resources Information Center

    Wallisch, Lynn S.; Liu, Liang Y.

    This booklet reports on the results of the 1998 Texas School Survey of Substance Use among Students: Grades 4-6. The statewide school survey monitors trends in substance use among public school students, identifies emerging problem areas, and serves as a basis of comparison for local school surveys which are conducted annually by various school…

  15. Travel On! Mini-Units and Learning Activities on Transportation for Grades 4-6.

    ERIC Educational Resources Information Center

    Lawson, Jane; And Others

    One of a series of eleven curriculum manuals which cover the four transportation topics of public transportation, transportation and the environment, transportation safety, and bicycles for elementary, secondary, and adult levels, this manual for grades 4-6 covers all four topics. Materials in four chapters comprising fourteen mini-units cover…

  16. 42 CFR 4.6 - Reference, bibliographic, reproduction, and consultation services.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 42 Public Health 1 2011-10-01 2011-10-01 false Reference, bibliographic, reproduction, and... SERVICES GENERAL PROVISIONS NATIONAL LIBRARY OF MEDICINE § 4.6 Reference, bibliographic, reproduction, and... request, reference, bibliographic, reproduction, and consultation services. Priority will be given...

  17. 42 CFR 4.6 - Reference, bibliographic, reproduction, and consultation services.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 42 Public Health 1 2014-10-01 2014-10-01 false Reference, bibliographic, reproduction, and... SERVICES GENERAL PROVISIONS NATIONAL LIBRARY OF MEDICINE § 4.6 Reference, bibliographic, reproduction, and... request, reference, bibliographic, reproduction, and consultation services. Priority will be given...

  18. 42 CFR 4.6 - Reference, bibliographic, reproduction, and consultation services.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 42 Public Health 1 2012-10-01 2012-10-01 false Reference, bibliographic, reproduction, and... SERVICES GENERAL PROVISIONS NATIONAL LIBRARY OF MEDICINE § 4.6 Reference, bibliographic, reproduction, and... request, reference, bibliographic, reproduction, and consultation services. Priority will be given...

  19. 42 CFR 4.6 - Reference, bibliographic, reproduction, and consultation services.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 42 Public Health 1 2013-10-01 2013-10-01 false Reference, bibliographic, reproduction, and... SERVICES GENERAL PROVISIONS NATIONAL LIBRARY OF MEDICINE § 4.6 Reference, bibliographic, reproduction, and... request, reference, bibliographic, reproduction, and consultation services. Priority will be given...

  20. 42 CFR 4.6 - Reference, bibliographic, reproduction, and consultation services.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 42 Public Health 1 2010-10-01 2010-10-01 false Reference, bibliographic, reproduction, and... SERVICES GENERAL PROVISIONS NATIONAL LIBRARY OF MEDICINE § 4.6 Reference, bibliographic, reproduction, and... request, reference, bibliographic, reproduction, and consultation services. Priority will be given...

  1. Steps Towards Healthy Growth. Health Education Curriculum Guide; Grades 4-6.

    ERIC Educational Resources Information Center

    Dippo, Jeanette, Ed.

    Grades or Ages: Grades 4-6. Subject Matter: Health Education (includes chapters covering the following: (a) health status; (b) nutrition; (c) sensory Perception; (d) dental health; (e) disease prevention and control; (f) smoking and health; (g) alcohol education; (h) drug education; (i) personality development; (j) human sexuality; (k) family life…

  2. Toxics in My Home? You Bet! Curriculum on Household Toxics for Grades 4-6.

    ERIC Educational Resources Information Center

    Purin, Gina; And Others

    This curriculum consists of a one-week course of study designed to introduce students in grades 4-6 to (or increase their awareness of) toxic substances commonly found in the home. It includes an introduction/conceptual framework, four lessons, a unit evaluation, and appendices. Each lesson consists of a statement of purpose, objectives,…

  3. The Navajo Way of Life: A Resource Unit with Activities for Grades 4-6.

    ERIC Educational Resources Information Center

    Cordova, Dahlia

    A resource unit on the Navajo way of life, for grades 4-6, contains sections on Navajo history, art, and crafts, homes, music, poetry and games; Navajo and Pueblo cookery (including recipes); traditional Navajo dress, ceremony and legends; and successful Navajos, past and present. Sections include text, vocabulary words, drawings, maps, and…

  4. The Uncomplicated Elementary Career Education System for the "Real" Classroom. Career Capers for 4-6.

    ERIC Educational Resources Information Center

    Illinois State Office of Education, Springfield. Div. of Adult Vocational and Technical Education.

    Prepared by classroom teachers for the infusion of career education into existing curriculum, this notebook of student and teacher activities is designed for use with the monthly Factivities for grades 4-6 (CE 023 596). Each activity corresponds to one of the nine monthly topics: "me, myself, and I"; exploring the telephone book; transportation;…

  5. BIOTRANSFORMATION OF 2,4,6-TRINITROTOLUENE (TNT) BY A PLANT-ASSOCIATED FUNGUS FUSARIUM OXYSPORUM

    EPA Science Inventory

    The capability of a plant-associated fungus, Fusarium oxyvorum, to transform TNT in liquid cultures was investigated. TNT was transformed into 2-amino-4, 6-dinitrotoluene (2-A-DNT), 4-amino-2, 6-dinitrotoluene (4-A- DNT), and 2, 4-diamino-6-nitrotoluene (2, 4-DAT) via 2- and 4-hy...

  6. SOIL REDUCES 2,4,6-TRINITROTOLUENE BIOAVAILABILITY AND GENOTOXICITY IN VIVO

    EPA Science Inventory

    Soil Reduces 2,4,6- Trinitrotoluene Bioavailability and Genotoxicity In Vivo

    As chemicals age in soil, irreversible binding of chemical contaminants to organic components in the soil may occur, impacting the amount of chemical that is biologically available upon exp...

  7. PCE/K-10 Activities for Career Education, Grades 4-6.

    ERIC Educational Resources Information Center

    Portland Public Schools, OR. Area II Office.

    The Portland (Oregon) Public School Project Career Education (PCE) Activities for grades 4-6 is based on the city's overall Area 2 program goals for career education which proposed that children completing school should have sufficient knowledge and competencies to enter into a field of employment or an advanced training program in that field.…

  8. Study of Vermont: A Curriculum Designed for Grades 4-6.

    ERIC Educational Resources Information Center

    Dubuque, Martha L.

    Designed for use in grades 4-6, this guide consists of four basic units related to the study of Vermont: Indian Civilization, Vermont History, Geography and Economics, and Cities and Towns. Each unit lists key concepts, content objectives, skills objectives, and related objectives. Next, specialized vocabulary as well as common, essential…

  9. Teaching Writing in Grades 4-6 in Urban Schools in the Greater China Region

    ERIC Educational Resources Information Center

    Hsiang, Tien Ping; Graham, Steve

    2016-01-01

    A random sample of 1102 grade 4-6 Chinese language arts teachers in Beijing, Macao, and Taipei City were surveyed about their instructional writing practices. Seventy-eight percent (n = 857) of the teachers completed the survey. Teachers were generally positive about the usefulness of their college teacher preparation program. They slightly agreed…

  10. Planet Patrol. An Environmental Unit on Solid Waste Solutions for Grades 4-6.

    ERIC Educational Resources Information Center

    Procter and Gamble Educational Services, Cincinnati, OH.

    This classroom unit was developed for use in grades 4-6 to help teach the concept of solid waste management. The teacher's guide provides an overview of the issue of solid waste disposal, a description of government, industry, and consumer roles in resolving the solid waste issue, and four lessons involving sanitary landfills, the reduction of…

  11. Overcoming Therapeutic Resistance in HER2-Positive Breast Cancers with CDK4/6 Inhibitors.

    PubMed

    Goel, Shom; Wang, Qi; Watt, April C; Tolaney, Sara M; Dillon, Deborah A; Li, Wei; Ramm, Susanne; Palmer, Adam C; Yuzugullu, Haluk; Varadan, Vinay; Tuck, David; Harris, Lyndsay N; Wong, Kwok-Kin; Liu, X Shirley; Sicinski, Piotr; Winer, Eric P; Krop, Ian E; Zhao, Jean J

    2016-03-14

    Using transgenic mouse models, cell line-based functional studies, and clinical specimens, we show that cyclin D1/CDK4 mediate resistance to targeted therapy for HER2-positive breast cancer. This is overcome using CDK4/6 inhibitors. Inhibition of CDK4/6 not only suppresses Rb phosphorylation, but also reduces TSC2 phosphorylation and thus partially attenuates mTORC1 activity. This relieves feedback inhibition of upstream EGFR family kinases, resensitizing tumors to EGFR/HER2 blockade. Consequently, dual inhibition of EGFR/HER2 and CDK4/6 invokes a more potent suppression of TSC2 phosphorylation and hence mTORC1/S6K/S6RP activity. The suppression of both Rb and S6RP enhances G1 arrest and a phenotype resembling cellular senescence. In vivo, CDK4/6 inhibitors sensitize patient-derived xenograft tumors to HER2-targeted therapies and delay tumor recurrence in a transgenic model of HER2-positive breast cancer. PMID:26977878

  12. 26 CFR 1.401(a)(4)-6 - Contributory defined benefit plans.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 26 Internal Revenue 5 2010-04-01 2010-04-01 false Contributory defined benefit plans. 1.401(a)(4...)-6 Contributory defined benefit plans. (a) Introduction. This section provides rules necessary for...) Excess plans with varying contribution rates. In the case of a defined benefit excess plan described...

  13. Spontaneous magnetization of the Ising model on the union jack and 4-6 lattices

    NASA Astrophysics Data System (ADS)

    Lin, K. Y.; Wang, S. C.

    1988-03-01

    Spontaneous magnetization of the Ising model on the anisotropic Union Jack and 4-6 lattices are derived exactly. The conjecture by Lin and Wang is confirmed. Our result is a generalization of the recent work on the isotropic Union Jack lattice by Choy and Baxter.

  14. The Synthesis of 4,6,8-Trimethylazulene: An Organic Laboratory Experiment.

    ERIC Educational Resources Information Center

    Garst, Michael E.; And Others

    1983-01-01

    A two-stage synthesis of 4,6,8-trimethylazulene was developed for use in the undergraduate experiment, highlighting concepts not usually covered in the laboratory. The experiment requires purification procedures of chromatography and of sublimation and illustrates concepts of aromaticity, molecular orbital theory, and carbodium ion reactivity. (JN)

  15. 43 CFR 2650.4-6 - National wildlife refuge system lands.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 43 Public Lands: Interior 2 2014-10-01 2014-10-01 false National wildlife refuge system lands... SELECTIONS Alaska Native Selections: Generally § 2650.4-6 National wildlife refuge system lands. (a) Every conveyance which includes lands within the national wildlife refuge system shall, as to such lands,...

  16. 43 CFR 2650.4-6 - National wildlife refuge system lands.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 43 Public Lands: Interior 2 2012-10-01 2012-10-01 false National wildlife refuge system lands... SELECTIONS Alaska Native Selections: Generally § 2650.4-6 National wildlife refuge system lands. (a) Every conveyance which includes lands within the national wildlife refuge system shall, as to such lands,...

  17. 43 CFR 2650.4-6 - National wildlife refuge system lands.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 43 Public Lands: Interior 2 2013-10-01 2013-10-01 false National wildlife refuge system lands... SELECTIONS Alaska Native Selections: Generally § 2650.4-6 National wildlife refuge system lands. (a) Every conveyance which includes lands within the national wildlife refuge system shall, as to such lands,...

  18. Preparation of 1,3,5-triamino-2,4,6-trinitrobenzene of submicron particle size

    DOEpatents

    Rigdon, Lester P.; Moody, Gordon L.; McGuire, Raymond R.

    2001-01-01

    A method is disclosed for the preparation of very small particle size, relatively pure 1,3,5-triamino-2,4,6-trinitrobenzene (TATB). Particles of TATB prepared according to the disclosed method are of submicron size and have a surface area in the range from about 3.8 to 27 square meters per gram.

  19. Preparation of 1,3,5-triamo-2,4,6-trinitrobenzene of submicron particle size

    DOEpatents

    Rigdon, Lester P.; Moody, Gordon L.; McGuire, Raymond R.

    2001-05-01

    A method is disclosed for the preparation of very small particle size, relatively pure 1,3,5-triamino-2,4,6-trinitrobenzene (TATB). Particles of TATB prepared according to the disclosed method are of submicron size and have a surface area in the range from about 3.8 to 27 square meters per gram.

  20. Absorption, balance and metabolism of /sup 14/C-2, 4, 6-trichlorophenol in hydroponic tomato plants

    SciTech Connect

    Fragiadakis, A.; Sotiriou, N.; Korte, F.

    1981-12-01

    Most of the 2, 4, 6-TCP applied in the nutrient solution of the hydroculture test was volatilised; a proportion was absorbed by the developed plant roots and to a small extent isomerised. Significant portions of the non-extractable tomato plant residues were found in the isolated lignin and cellulose fractions.

  1. A Curriculum in Written Composition, 4-6: A Guide for Teaching.

    ERIC Educational Resources Information Center

    Georgia Univ., Athens. English Curriculum Study Center.

    This guide for teaching composition in grades 4-6 (1) objectives for a curriculum in written composition, (2) sequence charts which relate subject content for each grade to basic understandings about composition, (3) illustrative learning experiences, and (4) units for teaching specific skills. The units for each grade are "Structuring a…

  2. TOXICITY OF TETRYL (N-METHYL-N,2,4,6-TETRANITROANILINE) IN F344 RATS

    EPA Science Inventory

    The toxicity of tetryl (N-methyl-N,2,4,6-tetranitroaniline) in male and female F344 rats was evaluated after adminstration in the diet for 14 or 90 days. The 14-day study diet concentrations used were 0, 500, 1250, 2000, 2500, and 5000 ppm; the 90-day study diet concentrations we...

  3. Kids, Crops, & Critters in the Classroom: An Agricultural Literacy Resource Guide for Grades 4-6.

    ERIC Educational Resources Information Center

    Illinois Farm Bureau, Bloomington.

    This resource guide provides teachers of grades 4-6 with ideas and materials to integrate agricultural concepts into classroom activities. The guide is organized into six categories: math, science, language arts, social studies, fine arts, and health/nutrition/safety. Each category contains 10 lessons organized in the following topic order:…

  4. Federal Aviation Administration Aviation Education Teacher's Guide, [Grades] 4-6.

    ERIC Educational Resources Information Center

    Federal Aviation Administration (DOT), Washington, DC.

    This guide is one in a series of four resource guides specifically designed for those interested in aviation education. Activities and lessons that can be used in a variety of content areas and grade levels are featured. Grades 4-6 are the focus of this guide, which is organized under the broad topics of properties of air, lighter than air flight,…

  5. Biotransformation of 2,4,6,8,10,12-Hexanitro-2,4,6,8,10,12-Hexaazaisowurtzitane (CL-20) by Denitrifying Pseudomonas sp. Strain FA1

    PubMed Central

    Bhushan, Bharat; Paquet, Louise; Spain, Jim C.; Hawari, Jalal

    2003-01-01

    The microbial and enzymatic degradation of a new energetic compound, 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane (CL-20), is not well understood. Fundamental knowledge about the mechanism of microbial degradation of CL-20 is essential to allow the prediction of its fate in the environment. In the present study, a CL-20-degrading denitrifying strain capable of utilizing CL-20 as the sole nitrogen source, Pseudomonas sp. strain FA1, was isolated from a garden soil. Studies with intact cells showed that aerobic conditions were required for bacterial growth and that anaerobic conditions enhanced CL-20 biotransformation. An enzyme(s) involved in the initial biotransformation of CL-20 was shown to be membrane associated and NADH dependent, and its expression was up-regulated about 2.2-fold in CL-20-induced cells. The rates of CL-20 biotransformation by the resting cells and the membrane-enzyme preparation were 3.2 ± 0.1 nmol h−1 mg of cell biomass−1 and 11.5 ± 0.4 nmol h−1 mg of protein−1, respectively, under anaerobic conditions. In the membrane-enzyme-catalyzed reactions, 2.3 nitrite ions (NO2−), 1.5 molecules of nitrous oxide (N2O), and 1.7 molecules of formic acid (HCOOH) were produced per reacted CL-20 molecule. The membrane-enzyme preparation reduced nitrite to nitrous oxide under anaerobic conditions. A comparative study of native enzymes, deflavoenzymes, and a reconstituted enzyme(s) and their subsequent inhibition by diphenyliodonium revealed that biotransformation of CL-20 is catalyzed by a membrane-associated flavoenzyme. The latter catalyzed an oxygen-sensitive one-electron transfer reaction that caused initial N denitration of CL-20. PMID:12957905

  6. Toxicity and photoactivation of PAH mixtures in marine sediment

    SciTech Connect

    Swartz, R.; Ferraro, S.; Lamberson, J.; Cole, F.; Ozretich, R.; Boese, B.; Schults, D.; Behrenfeld, M.; Ankley, G.

    1995-12-31

    The toxicity and toxicological photoactivation of mixtures of sediment-associated fluoranthene, phenanthrene, pyrene, and acenaphthene were determined using standard 10 d sediment toxicity tests with the marine amphipod, Rhepoxynius abronius. The four PAHs were spiked into sediment in a concentration series of either single compounds or an equitoxic mixture. Spiked sediment was stored at 4 C for 28 d before testing. Toxicity tests were conducted under fluorescent lighting. Survivors after 10 d in PAH-contaminated sediment were exposed for 1 h to UV light in the absence of sediment and then tested for their ability to bury in clean sediment. The 10 d LC50s for single PAHs were 3.3, 2.2, 2.8, and 2.3 mg/g oc for fluoranthene, phenanthrene, pyrene, and acenaphthene, respectively. These LC50s were used to calculate the sum of toxic units ({Sigma}TU) of the four PAHs in the equitoxic mixture treatments. The {Sigma}TU LC50 was then calculated for the mixture treatments. If the toxicological interaction of the four PAHs in the mixture was additive, the {Sigma}TU LC50 should equal 1.0. The observed {Sigma}TU LC50 in the mixture was 1.55, indicating the interaction was slightly less than additive. UV enhancement of toxic effects of individual PAHs was correctly predicted by photophysical properties, i.e. pyrene and fluoranthene were photoactivated and phenanthrene and acenaphthene were not. UV effects in the mixture of four PAHs can be explained by the photoactivation of pyrene and fluoranthene alone.

  7. New dust belts of Uranus: one ring, two ring, red ring, blue ring.

    PubMed

    de Pater, Imke; Hammel, Heidi B; Gibbard, Seran G; Showalter, Mark R

    2006-04-01

    We compared near-infrared observations of the recently discovered outer rings of Uranus with Hubble Space Telescope results. We find that the inner ring, R/2003 U 2, is red, whereas the outer ring, R/2003 U 1, is very blue. Blue is an unusual color for rings; Saturn's enigmatic E ring is the only other known example. By analogy to the E ring, R/2003 U 1 is probably produced by impacts into the embedded moon Mab, which apparently orbits at a location where nongravitational perturbations favor the survival and spreading of submicron-sized dust. R/2003 U 2 more closely resembles Saturn's G ring, which is red, a typical color for dusty rings. PMID:16601188

  8. Saturn's F-Ring

    NASA Technical Reports Server (NTRS)

    2000-01-01

    This narrow-angle camera image of Saturn's F Ring was taken through the Clear filter while at a distance of 6.9 million km from Saturn on 8 November 1980. The brightness variations of this tightly-constrained ring shown here indicate that the ring is less uniform in makeup than the larger rings. JPL managed the Voyager Project for NASA's Office of Space Science

  9. Neptune - full ring system

    NASA Technical Reports Server (NTRS)

    1989-01-01

    This pair of Voyager 2 images (FDS 11446.21 and 11448.10), two 591-s exposures obtained through the clear filter of the wide angle camera, show the full ring system with the highest sensitivity. Visible in this figure are the bright, narrow N53 and N63 rings, the diffuse N42 ring, and (faintly) the plateau outside of the N53 ring (with its slight brightening near 57,500 km).

  10. 17 CFR 4.6 - Exclusion for certain otherwise regulated persons from the definition of the term “commodity...

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... otherwise regulated persons from the definition of the term âcommodity trading advisor.â 4.6 Section 4.6 Commodity and Securities Exchanges COMMODITY FUTURES TRADING COMMISSION COMMODITY POOL OPERATORS AND COMMODITY TRADING ADVISORS General Provisions, Definitions and Exemptions § 4.6 Exclusion for...

  11. Analyses of the Effects of Global Change on Human Health and Welfare and Human Systems (SAP 4.6)

    EPA Science Inventory

    EPA has announced the final report entitled, Synthesis and Assessment Product 4.6: Analyses of the Effects of Global Change on Human Health and Welfare and Human Systems . This Synthesis and Assessment Product 4.6 (SAP 4.6) focuses on impacts of global climate change, es...

  12. Saturn's F-Ring

    NASA Technical Reports Server (NTRS)

    2000-01-01

    This narrow-angle camera image of Saturn's F Ring was taken through the Clear filter while at a distance of 0.75 million km from Saturn on 12 November 1980. The kinks and braids of this tightly-constrained ring are visible along with the outer edge of the A Ring. JPL managed the Voyager Project for NASA's Office of Space Science.

  13. The Jumping Ring Experiment

    ERIC Educational Resources Information Center

    Baylie, M.; Ford, P. J.; Mathlin, G. P.; Palmer, C.

    2009-01-01

    The jumping ring experiment has become central to liquid nitrogen shows given as part of the outreach and open day activities carried out within the University of Bath. The basic principles of the experiment are described as well as the effect of changing the geometry of the rings and their metallurgical state. In general, aluminium rings are…

  14. Rings Around Uranus

    ERIC Educational Resources Information Center

    Maran, Stephen P.

    1977-01-01

    Events leading up to the discovery of the rings of Uranus are described. The methods used and the logic behind the methods are explained. Data collected to prove the existence of the rings are outlined and theories concerning the presence of planetary rings are presented. (AJ)

  15. Occurrence and source apportionment of PAHs in highly vulnerable karst system.

    PubMed

    Shao, Yixian; Wang, Yanxin; Xu, Xiaoqing; Wu, Xiao; Jiang, Zhou; He, Shanshan; Qian, Kun

    2014-08-15

    The concentration and spatial distribution of polycyclic aromatic hydrocarbons (PAHs) in topsoil, groundwater and groundwater suspended solids (SS) at Guozhuang karst water system of northern China were investigated. The total concentration of PAHs ranged from 622 to 87,880 ng/g dry weight in topsoil, from 4739 to 59,314 ng/g dry weight in SS, and from 2137 to 9037 ng/L in groundwater, with mean values of 17,174 ng/g, 11,990 ng/g and 5020 ng/L, respectively. High concentrations of PAHs were mainly observed in the coal mining industrial area and the discharge area. The composition of PAHs indicated that low molecular weight PAHs were predominant in groundwater samples, the content of medium molecular weight PAHs was elevated in SS, and carcinogenic high molecular weight PAHs were frequently detected in topsoil. The high contents of low-medium molecular weight PAHs in groundwater and SS suggested relatively recent local sources of PAHs that were transported into the aquifer via leakage of contaminated surface water and/or infiltration of PAH-containing precipitation. The results of evaluating sources of PAHs using ratios of specific PAH compounds showed that PAHs mainly originated from coal and wood combustion. Furthermore, five sources were identified by positive matrix factorization (PMF) model, and the contribution to the total loadings of groundwater PAHs were: 2% for unburnt oil, 32% for coal combustion, 22% for vehicle emission, 27% for biomass combustion and 18% for coke production, respectively. Furthermore, strong correlations of total PAHs with total organic carbon (TOC) in topsoil indicated co-emission of PAHs and TOC. Poor correlations of PAHs with dissolved organic carbon (DOC) in groundwater indicated that other factors exert stronger influences. Therefore, PAHs might have posed a major threat to the quality of potable groundwater in Guozhuang karst water system. PMID:24852613

  16. 2-(4-Amino-benzene-sulfonamido)-4,6-dimethyl-pyrimidin-1-ium 2-carb-oxy-4,6-dinitro-phenolate.

    PubMed

    Smith, Graham; Wermuth, Urs D

    2013-04-01

    In the structure of the phenolate salt of the sulfa drug sulfamethazine with 3,5-dinitro-salicylic acid, C12H15N4O2S(+)·C7H3N2O7 (-), the dihedral angle between the pyrimidine and benzene rings of the cation is 59.70 (17)°. In the crystal, cation-anion hydrogen-bonding inter-actions involving pyrim-idine-carb-oxy N(+)-H⋯O and amine-carb-oxy N-H⋯O pairs give a cyclic R 2 (2)(8) motif while secondary N-H⋯O hydrogen bonds between the aniline group and both sulfone and nitro O-atom acceptors give a two-dimensional structure extending in (001). PMID:23634030

  17. Substituent effects on the properties related to detonation performance and sensitivity for 2,2',4,4',6,6'-hexanitroazobenzene derivatives.

    PubMed

    Liu, Yan; Gong, Xuedong; Wang, Lianjun; Wang, Guixiang; Xiao, Heming

    2011-03-10

    To look for superior and safe high energy density compounds (HEDCs), 2,2',4,4',6,6'-hexanitroazobenzene (HNAB) and its -NO(2), -NH(2), -CN, -NC, -ONO(2), -N(3), or -NF(2) derivatives were studied at the B3LYP/6-31G* level of density functional theory (DFT). The isodesmic reactions were applied to calculate the heats of formation (HOFs) for these compounds. The theoretical molecular density (ρ), detonation energy (E(d)), detonation pressure (P), and detonation velocity (D), estimated using the Kamlet-Jacobs equations, showed that the detonation properties of these compounds were excellent. The effects of substituent groups on HOF, ρ, E(d), P, and D were studied. The order of contribution of the substituent groups to P and D was -NF(2) > -ONO(2) > -NO(2) > -N(3) > -NH(2). Sensitivity was evaluated using the nitro group charges, frontier orbital energies, and bond dissociation enthalpies (BDEs). The trigger bonds in the pyrolysis process for all these HNAB derivatives may be Ring-NO(2), Ring-N═N, Ring-NF(2), or O-NO(2) varying with the attachment of different substituents. BDEs of trigger bonds except those of -ONO(2) derivatives are relatively large, which means these compounds suffice the stability request of explosives. Taking both detonation properties and sensitivities into consideration, some -NF(2) and -NO(2) derivatives may be potential candidates for HEDCs. PMID:21314160

  18. Jovian Ring System Mosaic

    NASA Technical Reports Server (NTRS)

    2000-01-01

    NASA's Galileo spacecraft acquired this mosaic of Jupiter's ring system (top) when the spacecraft was in Jupiter's shadow looking back toward the Sun. Jupiter's ring system (inset diagram) is composed of three parts: an outermost gossamer ring, a flat main ring, and an innermost donut-shaped halo. These rings are made up of dust-sized particles that are blasted off of the nearby inner satellites by small impacts. This image was taken on November 9, 1996 at a distance of 2.3 million kilometers (1.4 million miles).

  19. Emission characterization and δ(13)C values of parent PAHs and nitro-PAHs in size-segregated particulate matters from coal-fired power plants.

    PubMed

    Wang, Ruwei; Yousaf, Balal; Sun, Ruoyu; Zhang, Hong; Zhang, Jiamei; Liu, Guijian

    2016-11-15

    The objective of this study was to characterize parent polycyclic aromatic hydrocarbons (pPAHs) and their nitrated derivatives (NPAHs) in coarse (PM2.5-10), intermediate (PM1-2.5) and fine (PM1) particulate matters emitted from coal-fired power plants (CFPPs) in Huainan, China. The diagnostic ratios and the stable carbon isotopic approaches to characterize individual PAHs were applied in order to develop robust tools for tracing the origins of PAHs in different size-segregated particular matters (PMs) emitted CFPP coal combustion. The concentrations of PAH compounds in flue gas emissions varied greatly, depending on boiler types, operation and air pollution control device (APCD) conditions. Both pPAHs and NPAHs were strongly enriched in PM1-2.5 and PM1. In contrary to low molecular weight (LMW) PAHs, high molecular weight (HMW) PAHs were more enriched in finer PMs. The PAH diagnostic ratios in size-segregated PMs are small at most cases, highlighting their potential application in tracing CFPP emitted PAHs attached to different sizes of PMs. Yet, substantial uncertainty still exists to directly apply PAH diagnostic ratios as emission tracers. Although the stable carbon isotopic composition of PAH molecular was useful in differentiating coal combustion emissions from other sources such as biomass combustion and vehicular exhausts, it was not feasible to differentiate isotopic fractionation processes such as low-temperature carbonization, high-temperature carbonization, gasification and combustion. PMID:27450341

  20. Saturn's largest ring.

    PubMed

    Verbiscer, Anne J; Skrutskie, Michael F; Hamilton, Douglas P

    2009-10-22

    Most planetary rings in the Solar System lie within a few radii of their host body, because at these distances gravitational accelerations inhibit satellite formation. The best known exceptions are Jupiter's gossamer rings and Saturn's E ring, broad sheets of dust that extend outward until they fade from view at five to ten planetary radii. Source satellites continuously supply the dust, which is subsequently lost in collisions or by radial transport. Here we report that Saturn has an enormous ring associated with its outer moon Phoebe, extending from at least 128R(S) to 207R(S) (Saturn's radius R(S) is 60,330 km). The ring's vertical thickness of 40R(S) matches the range of vertical motion of Phoebe along its orbit. Dynamical considerations argue that these ring particles span the Saturnian system from the main rings to the edges of interplanetary space. The ring's normal optical depth of approximately 2 x 10(-8) is comparable to that of Jupiter's faintest gossamer ring, although its particle number density is several hundred times smaller. Repeated impacts on Phoebe, from both interplanetary and circumplanetary particle populations, probably keep the ring populated with material. Ring particles smaller than centimetres in size slowly migrate inward and many of them ultimately strike the dark leading face of Iapetus. PMID:19812546

  1. Characterization of PAHs within PM 10 fraction for ashes from coke production, iron smelt, heating station and power plant stacks in Liaoning Province, China

    NASA Astrophysics Data System (ADS)

    Kong, Shaofei; Shi, Jianwu; Lu, Bing; Qiu, Weiguang; Zhang, Baosheng; Peng, Yue; Zhang, Bowen; Bai, Zhipeng

    2011-07-01

    Polycyclic aromatic hydrocarbons within PM 10 fraction of ashes from two coke production plants, one iron smelt plant, one heating station and one power plant were analyzed with GC-MS technique in 2009. The sum of 17 selected PAHs varied from 290.20 to 7055.72 μg/g and the amounts of carcinogenic PAHs were between 140.33 and 3345.46 μg/g. The most toxic ash was from the coke production plants and then from the iron smelt plant, coal-fired power plant and heating station according to BaP-based toxic equivalent factor (BaPeq) and BaP-based equivalent carcinogenic power (BaPE). PAHs profile of the iron smelt ash was significantly different from others with coefficient of divergence value higher than 0.40. Indicatory PAHs for coke production plants, heating station and coal-fired power plant were mainly 3-ring species such as Acy, Fl and Ace. While for iron smelt plant, they were Chr and BbF. Diagnostic ratios including Ant/(Ant + Phe), Flu/(Flu + Pyr), BaA/Chr, BbF/BkF, Ind/BghiP, IND/(IND + BghiP), BaP/BghiP, BaP/COR, Pyr/BaP, BaA/(BaA + Chr), BaA/BaP and BaP/(BaP + Chr) were calculated which were mostly different from other stacks for the iron smelt plant.

  2. The hydrogen bond in 2-( N,N-dimethylamino- N-oxymethyl)-4,6-dimethylophenol

    NASA Astrophysics Data System (ADS)

    Rospenk, M.; Koll, A.; Głowiak, T.; Sobczyk, L.

    1989-04-01

    The X-ray diffraction studies have been carried out on the monohydrate of 2-( N,N-dimethylamino- N-oxymethyl)-4,6-dimethylophenol ( I). The crystals are monoclinic, space group P2 1/c, with a = 21.921(6) Å, b = 5.058(2) Å, c = 11.748(3) Å; β = 113.66(4)°, V = 1193.1(4) Å 3, Z = 4. The length of the intramolecular OH⋯O hydrogen bond is 2.541(6) Å. The crystallographic data and the UV and IR absorption spectra indicate that this bond is considerably weaker than that reported previously for 2-( N,N-diethylamino- N-oxymethyl)-4,6-dichlorophenol ( II), where a quasisymmetric bridge was found.

  3. A large-scale evaluation of the KiVa antibullying program: grades 4-6.

    PubMed

    Kärnä, Antti; Voeten, Marinus; Little, Todd D; Poskiparta, Elisa; Kaljonen, Anne; Salmivalli, Christina

    2011-01-01

    This study demonstrates the effectiveness of the KiVa antibullying program using a large sample of 8,237 youth from Grades 4-6 (10-12 years). Altogether, 78 schools were randomly assigned to intervention (39 schools, 4,207 students) and control conditions (39 schools, 4,030 students). Multilevel regression analyses revealed that after 9 months of implementation, the intervention had consistent beneficial effects on 7 of the 11 dependent variables, including self- and peer-reported victimization and self-reported bullying. The results indicate that the KiVa program is effective in reducing school bullying and victimization in Grades 4-6. Despite some evidence against school-based interventions, the results suggest that well-conceived school-based programs can reduce victimization. PMID:21291444

  4. Multiple Roles of Cyclin-Dependent Kinase 4/6 Inhibitors in Cancer Therapy

    PubMed Central

    Roberts, Patrick J.; Bisi, John E.; Strum, Jay C.; Combest, Austin J.; Darr, David B.; Usary, Jerry E.; Zamboni, William C.; Wong, Kwok-Kin; Perou, Charles M.

    2012-01-01

    Background Cyclin-dependent kinases (CDKs) regulate cell proliferation and coordinate the cell cycle checkpoint response to DNA damage. Although inhibitors with varying selectivity to specific CDK family members have been developed, selective CDK4/6 inhibitors have emerged as the most attractive antineoplastic agents because of the importance of CDK4/6 activity in regulating cell proliferation and the toxic effects associated with inhibition of other CDKs (eg, CDK1 and CDK2). Methods FVB/N wild-type mice (n = 13) were used to evaluate carboplatin-induced myelosuppression in bone marrow by complete blood cell counts after treatment with the CDK4/6 inhibitor PD0332991. Genetically engineered murine models of retinoblastoma (Rb)-competent (MMTV-c-neu) and Rb-incompetent (C3-TAg) breast cancer (n = 16 MMTV-c-neu mice in the carboplatin plus vehicle control group, n = 17 MMTV-c-neu mice in the carboplatin plus PD0332991 group, n = 17 C3-TAg mice in the carboplatin plus vehicle control group, and n = 14 C3-TAg mice in the carboplatin plus PD0332991 group) were used to investigate the antitumor activity of PD0332991 alone or in combination with chemotherapy. All statistical tests were two-sided. Results Coadministration of PD0332991 with carboplatin compared with carboplatin alone in FVB/N wild-type mice increased hematocrit (51.2% vs 33.5%, difference = 17.7%, 95% confidence interval [CI] = −26.7% to −8.6%, P < .001), platelet counts (1321 vs 758.5 thousand cells per μL, difference = 562.5 thousand cells per μL, 95% CI = −902.8 to −222.6, P = .002), myeloid cells (granulocytes and monocytes; 3.1 vs 1.6 thousand cells per μL, difference = 1.5 thousand cells per μL, 95% CI = −2.23 to −0.67, P < .001), and lymphocytes (7.9 vs 5.4 thousand cells per μL, difference = 2.5 thousand cells per μL, 95% CI = −4.75 to −0.18, P = .02). Daily administration of PD0332991 exhibited antitumor activity in MMTV-c-neu mice as a single agent. However, the combination of

  5. Decreased transpiration in poplar trees exposed to 2,4,6-trinitrotoluene

    SciTech Connect

    Thompson, P.L.; Ramer, L.A.; Guffey, A.P.; Schnoor, J.L.

    1998-01-01

    The improper handling of the toxic compound 2,4,6-trinitrotoluene (TNT) has led to the contamination of soil and groundwater, and the uptake of TNT by a variety of plants has been established. This article discusses the effects of various concentrations of the explosive 2,4,6-trinitrotoluene (TNT) on the transpiration of hybrid poplar trees growing in hydroponic media. Transpiration was measured daily by gravimetric means. The rapid removal of TNT from hydroponic solutions was a result of plant uptake and required a daily dosage of TNT to ensure a relatively constant exposure over time. Transpiration decreased with increasing TNT concentrations {ge}5 mg/L. Decreases in transpiration were accompanied by leaf chlorosis and abscission. A comparison between a laboratory study and a pilot-scale experiment showed good scale-up potential.

  6. PAHs in circumstellar disks around T Tauri stars

    NASA Astrophysics Data System (ADS)

    Geers, Vincent C.; Augereau, Jean-Charles; Pontoppidan, Klaus M.; Dullemond, Cornelis P.; Visser, Ruud; van Dishoeck, Ewine F.; C2d Irs Team

    We have begun to investigate the emission from Polycyclic Aromatic Hydrocarbons seen toward circumstellar disks around young low mass pre-main-sequence (T Tauri) stars, observed as part of our Spitzer Legacy program "From Molecular Cores to Planet-Forming Disks" (Evans et al. 2003). In this poster we will present some of our first Spitzer spectra of PAH features in T Tauri stars and discuss these features in the context of the disk structure and the UV radiation field needed to excite the PAH molecules. Laboratory measurements show that PAH molecules are strongly heated/excited when they absorb a single UV photon, and that they re-radiate the energy through C-H and C-C stretch and C-H bending mode transitions, in the form of infrared photons. These give rise to characteristic PAH features at 3.3, 6.2, 7.7, 8.6, 11.2 and 12.8 microns. These emission features have now been observed toward about 60% of intermediate mass Herbig Ae/Be stars with the ISO satellite (Acke & van den Ancker 2004) and for a few of these sources, ground-based spatially resolved spectroscopy has confirmed that the emission originates from the inner ~100-150 AU region around the star (Geers et al. 2004, van Boekel et al. 2004, Habart et al. 2004), so typically on the scale of circumstellar disks. Our investigation of PAHs in disks around young stars takes two approaches. On the one hand, we address the question how the PAH abundance evolves in these disks during this period of planet formation and how their presence can have an impact on the circumstellar environment. The observed PAH emission is believed to originate from the surface layers of the disk, where the large molecules / small grains are mixed with the gas. The high opacity of PAHs to FUV radiation can significantly reduce the stellar UV field in the inner parts of the disk, while at the same time, through the photo-electric effect, PAHs can provide an important heating mechanism for the gas in the surrounding environment through

  7. Interstellar PAH Emission in the 11-14 micron Region: New Insights and a Tracer of Ionized PAHs

    NASA Technical Reports Server (NTRS)

    Hudgins, Douglas M.; Allamandola, Louis J.; Mead, Susan (Technical Monitor)

    1999-01-01

    The Ames infrared spectral database of isolated, neutral and ionized polycyclic aromatic hydrocarbons (PAHs) shows that aromatic CH out-of-plane bending frequencies are significantly shifted upon ionization. For non-adjacent and doubly-adjacent CH groups, the shift is pronounced and consistently toward higher frequencies. The non-adjacent modes are blueshifted by an average of 27 per cm and the doubly-adjacent modes by an average of 17 per cm. For triply- and quadruply-adjacent CH out-of-plane modes the ionization shifts are more erratic and typically more modest. As a result of these ionization shifts, both the non-adjacent and doubly-adjacent CH out-of-plane modes move out of the regions classically associated with their respective vibrations in neutral PAHs. The doubly-adjacent modes of ionized PAHs tend to fall into the frequency range traditionally associated with the non-adjacent modes, while the non-adjacent modes are shifted to frequencies above those normally attributed to out-of-plane bending vibrations. Consequently, the origin of the interstellar infrared emission feature near 11.2 microns, traditionally attributed to the out-of-plane bending of non-adjacent CH groups on PAHs is rendered ambiguous. Instead, this feature likely reflects contributions from both non-adjacent CH units in neutral PAHs and doubly-adjacent CH units in PAH cations, the dominant charge state in the most energetic emission regions. This greatly relieves the structural constraints placed on the interstellar PAH population by the dominance of the 11.2 micron band in this region and eliminates the necessity to invoke extensive dehydrogenation of the emitting species. Furthermore, these results indicate that the emission between 926 and 904 per cm (10.8 and 11.1 microns) observed in many sources can be unambiguously attributed to the non-adjacent CH out-of-plane bending modes of moderately-sized (fewer than 50 carbon atom) PAH cations making this emission an unequivocal tracer of

  8. Electronic structure and spectral-luminescent properties of 1,2,4,6-tetrasubstituted pyridinium salts

    SciTech Connect

    Korunova, A.F.; Krainov, I.P.; Protsenko, E.G.

    1985-09-01

    The structure of the electronic excitation of 1,2,4,6-tetrasubstituted pyridinium salts was studied by quantum-chemical calculations carried out by the SCF PPP CI method, using excitation-localization numbers on the atoms and fragments, and interfragmentary charge transfer numbers. The nature of the absorption bands observed in the spectra and certain structural factors causing the spectral-luminescent properties were established.

  9. Spot test for 1,3,5-triamino-2,4,6-trinitrobenzene, TATB

    DOEpatents

    Harris, B.W.

    1984-11-29

    A simple, sensitive and specific spot test for 1,3,5-triamino-2,4,6-trinitrobenzene, TATB, is described. Upon the application of the composition of matter of the subject invention to samples containing in excess of 0.1 mg of this explosive, a bright orange color results. Interfering species such as TNT and Tetryl can be removed by first treating the sample with a solvent which does not dissolve the TATB, but readily dissolves these interfering explosives.

  10. Spot test for 1,3,5-triamino-2,4,6-trinitrobenzene, TATB

    DOEpatents

    Harris, Betty W.

    1986-01-01

    A simple, sensitive and specific spot test for 1,3,5-triamino-2,4,6-trinitrobenzene, TATB, is described. Upon the application of the composition of matter of the present invention to samples containing in excess of 0.1 mg of this explosive, a bright orange color results. Interfering species such as TNT and Tetryl can be removed by first treating the sample with a solvent which does not dissolve much of the TATB, but readily dissolves these explosives.

  11. Reflectance spectra of mafic silicates and phyllosilicates from .6 to 4.6 microns

    NASA Technical Reports Server (NTRS)

    Roush, Ted L.; Singer, Robert B.; Mccord, Thomas B.

    1987-01-01

    The results of spectral measurements for mafic silicates are given. The study provided valuable spectral reflectance information about mafic silicates and phyllosilicates in the 2.5 to 4.6 micron wavelength region. It was shown that the reflectance of these materials is strongly affected by the presence of H2O and OH. Therefore, the identification of these absorbing species is greatly enhanced.

  12. Simulation of atmospheric PAH emissions from diesel engines.

    PubMed

    Durán, A; de Lucas, A; Carmona, M; Ballesteros, R

    2001-08-01

    Simulation of atmospheric PAH emissions in a typical European passenger car diesel engine at steady conditions or under a certification cycle is made using in-house software. It is based on neural fitting of experimental data from eight different fuels tested under five operating steady conditions (reproducing modes of the European transient urban/extraurban certification cycle). The software allows the determination of PAH emissions as a function of the fuel composition parameters (aromatic content, cetane index, gross heat power, nitrogen and sulphur content) and operation conditions (torque and engine speed). The mathematical model reproduces experimental data with a maximum error of 20%. This tool is very useful, since changes in parameters can be made without experimental cost and the trend in modifications in PAH emissions is immediately obvious. PMID:11513424

  13. Spectroscopic properties of polycyclic aromatic hydrocarbons (PAHs) and astrophysical implications.

    PubMed

    d'Hendecourt, L; Ehrenfreund, P

    1997-01-01

    PAHs (polycyclic aromatic hydrocarbons) are probably present as a mixture of neutral and ionized species and are responsible for the set of infrared emission bands in the 2-15 microns regions, which are observed in many different objects like reflection and planetary nebulae and external galaxies. PAHs are suggested to be the most abundant free organic molecules and ubiquitous in space. PAHs might also exist in the solid phase, included in interstellar ices in dense clouds. A complex aromatic network is expected on interstellar grains in the diffuse interstellar medium. The existence of an aromatic kerogen-like structure in carbonaceous meteorites and its similarity with interstellar spectra suggests a link between interstellar matter and primitive Solar System bodies. PMID:11541329

  14. Spitzer Observations of Extraplanar PAH Emission from Spiral Galaxies

    NASA Astrophysics Data System (ADS)

    Lehner, N.; Howk, J.

    We present Spitzer/IRAC observations of polycylic aromatic hydrocarbon (PAH) emission from interstellar material in the thick disks of normal spiral galaxies. These data show PAHs to be a common constituent of extraplanar material in spirals. The processes that displace this material from the interstellar disks of these systems do not destroy these very small grains. The dust emission features are present far above the galactic planes, extended up to about 2-4 kpc above the midplanes of the galaxies presented in this work. The total extent for which dust can be traced is about half the extent of the DIG. If it is not a sensitivity effect, this suggests that PAHs may be associated with a cold neutral medium that can not be supported at high z.

  15. [Health risk assessment of coke oven PAHs emissions].

    PubMed

    Bo, Xin; Wang, Gang; Wen, Rou; Zhao, Chun-Li; Wu, Tie; Li, Shi-Bei

    2014-07-01

    Polycyclic aromatic hydrocarbons (PAHs) produced by coke oven are with strong toxicity and carcinogenicity. Taken typical coke oven of iron and steel enterprises as the case study, the dispersion and migration of 13 kinds of PAHs emitted from coke oven were analyzed using AERMOD dispersion model, the carcinogenic and non-carcinogenic risks at the receptors within the modeling domain were evaluated using BREEZE Risk Analyst and the Human Health Risk Assessment Protocol for Hazardous Waste Combustion (HHRAP) was followed, the health risks caused by PAHs emission from coke oven were quantitatively evaluated. The results indicated that attention should be paid to the non-carcinogenic risk of naphthalene emission (the maximum value was 0.97). The carcinogenic risks of each single pollutant were all below 1.0E-06, while the maximum value of total carcinogenic risk was 2.65E-06, which may have some influence on the health of local residents. PMID:25244863

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

    PubMed

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

    2017-01-15

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

  17. 2,4,6-Trichloroanisole is a potent suppressor of olfactory signal transduction

    PubMed Central

    Takeuchi, Hiroko; Kato, Hiroyuki; Kurahashi, Takashi

    2013-01-01

    We investigated the sensitivity of single olfactory receptor cells to 2,4,6-trichloroanisole (TCA), a compound known for causing cork taint in wines. Such off-flavors have been thought to originate from unpleasant odor qualities evoked by contaminants. However, we here show that TCA attenuates olfactory transduction by suppressing cyclic nucleotide-gated channels, without evoking odorant responses. Surprisingly, suppression was observed even at extremely low (i.e., attomolar) TCA concentrations. The high sensitivity to TCA was associated with temporal integration of the suppression effect. We confirmed that potent suppression by TCA and similar compounds was correlated with their lipophilicity, as quantified by the partition coefficient at octanol/water boundary (pH 7.4), suggesting that channel suppression is mediated by a partitioning of TCA into the lipid bilayer of plasma membranes. The rank order of suppression matched human recognition of off-flavors: TCA equivalent to 2,4,6-tribromoanisole, which is much greater than 2,4,6-trichlorophenol. Furthermore, TCA was detected in a wide variety of foods and beverages surveyed for odor losses. Our findings demonstrate a potential molecular mechanism for the reduction of flavor. PMID:24043819

  18. p18 inhibits reprogramming through inactivation of Cdk4/6

    PubMed Central

    Zhu, Shaohua; Cao, Jiani; Sun, Hongyan; Liu, Kun; Li, Yaqiong; Zhao, Tongbiao

    2016-01-01

    Pluripotent stem cells (PSCs), including embryonic and induced pluripotent stem cells (iPSCs), show atypical cell cycle regulation characterized by a high proliferation rate and a shorter G1 phase compared with somatic cells. The mechanisms by which somatic cells remodel their cell cycle to achieve the high proliferation rate of PSCs during reprogramming are unclear. Here we identify that the Ink4 protein p18, which is expressed at high levels in somatic cells but at low levels in PSCs, is a roadblock to successful reprogramming. Mild inhibition of p18 expression enhances reprogramming efficiency, while ectopic expression of p18 completely blocks reprogramming. Mechanistic studies show that expression of wild-type p18, but not a p18D68N mutant which cannot inhibit Cdk4/6, down-regulates expression of Cdk4/6 target genes involved in DNA synthesis (TK, TS, DHFR, PCNA) and cell cycle regulation (CDK1 and CCNA2) and thus inhibits reprogramming. These results indicate that p18 blocks reprogramming by targeting Cdk4/6-mediated cell cycle regulation. Taken together, our results define a novel pathway that inhibits somatic cell reprogramming, and provide a new target to enhance reprogramming efficiency. PMID:27484146

  19. New double molybdate Na9Fe(MoO4)6: Synthesis, structure, properties

    NASA Astrophysics Data System (ADS)

    Savina, Aleksandra A.; Solodovnikov, Sergey F.; Basovich, Olga M.; Solodovnikova, Zoya A.; Belov, Dmitry A.; Pokholok, Konstantin V.; Gudkova, Irina A.; Stefanovich, Sergey Yu.; Lazoryak, Bogdan I.; Khaikina, Elena G.

    2013-09-01

    A new double molybdate Na9Fe(MoO4)6 was synthesized using solid state reactions and studied with X-ray powder diffraction, second harmonic generation (SHG) technique, differential scanning calorimetry, X-ray fluorescence analysis, Mössbauer and dielectric impedance spectroscopy. Single crystals of Na9Fe(MoO4)6 were obtained and its structure was solved (the space group R3¯, a=14.8264(2), c=19.2402(3) Å, V=3662.79(9) Å3, Z=6, R=0.0132). The structure is related to that of sodium ion conductor II-Na3Fe2(AsO4)3. The basic structure units are polyhedral clusters composed of central FeО6 octahedron sharing edges with three Na(1)О6 octahedra. The clusters share common vertices with bridging МоО4 tetrahedra to form an open 3D framework where the cavities are occupied by Na(2) and Na(3) atoms. The compound melts incongruently at 904.7±0.2 K. Arrhenius type temperature dependence of electric conductivity σ has been registered in solid state (σ=6.8×10-2 S сm-1 at 800 K), thus allowing considering Na9Fe(MoO4)6 as a new sodium ion conductor.

  20. CDK4/6 Inhibitor PD0332991 in Glioblastoma Treatment: Does It Have a Future?

    PubMed Central

    Schröder, Lisette B. W.; McDonald, Kerrie L.

    2015-01-01

    Glioblastoma is aggressive, highly infiltrating, and the most frequent malignant form of brain cancer. With a median survival time of only 14.6 months, when treated with the standard of care, it is essential to find new therapeutic options. A specific CDK4/6 inhibitor, PD0332991, obtained accelerated approval from the Food and Drug Administration for the treatment of patients with advanced estrogen receptor-positive and HER2-negative breast cancer. Common alterations in the cyclin D1-cyclin-dependent kinase 4/6-retinoblastoma 1 pathway in glioblastoma make PD0332991 also an interesting drug for the treatment of glioblastoma. Promising results in in vitro studies, where patient derived glioblastoma cell lines showed sensitivity to PD0332991, gave motive to start in vivo studies. Outcomes of these studies have been contrasting in terms of PD0332991 efficacy within the brain: more research is necessary to conclude whether CDK4/6 inhibitor can be beneficial in the treatment of glioblastoma. PMID:26649278

  1. Polycyclic aromatic hydrocarbons (PAHs), nitro-PAHs and related environmental compounds: biological markers of exposure and effects.

    PubMed Central

    Talaska, G; Underwood, P; Maier, A; Lewtas, J; Rothman, N; Jaeger, M

    1996-01-01

    Lung cancer caused by polycyclic aromatic hydrocarbons (PAHs), nitro-PAHs and related environmental agents is a major problem in industrialized nations. The high case-fatality rate of the disease, even with the best supportive treatment, underscores the importance of primary lung cancer prevention. Development of biomarkers of exposure and effects to PAHs and related compounds is now underway and includes measurement of urinary metabolites of specific PAHs as well as detection of protein and DNA adducts as indicators of effective dose. Validation of these markers in terms of total environmental dose requires that concurrent measures of air levels and potential dermal exposure be made. In addition, the interrelationships between PAH biomarkers must be determined, particularly when levels of the marker in surrogate molecules (e.g., protein) or markers from surrogate tissues (e.g., lymphocyte DNA) are used to assess the risk to the target organ, the lung. Two approaches to biomarker studies will be reviewed in this article: the progress made using blood lymphocytes as surrogates for lung tissues and the progress made developing noninvasive markers of carcinogen-DNA adduct levels in lung-derived cells available in bronchial-alveolar lavage and in sputum. Data are presented from studies in which exfoliated urothelial cells were used as a surrogate tissue to assess exposure to human urinary bladder carcinogens in occupational groups. PMID:8933032

  2. A record of polycyclic aromatic hydrocarbon (PAH) pollution obtained from accreting sediments of the Tamar Estuary, U.K.: evidence for non-equilibrium behaviour of PAH.

    PubMed

    Readman, J W; Mantoura, R F; Rhead, M M

    1987-10-01

    Concentrations of polycyclic aromatic hydrocarbons (PAH) were quantified throughout a 210Po-dated inter-tidal sediment core from the Tamar Estuary, U.K. in order to reconstruct the input history and investigate environmental reactivity of PAH in sediments. The profile recorded is similar to those reported in other aquatic sedimentary studies, with an approximately exponential increase in the concentrations of individual PAH from less than 30 ng (g dry sediment)-1 prior to 1940 to between 100 and 1000 ng (g dry sediment)-1 in contemporary surface sediments. This corresponds to an increased input of total PAH from 0.23 to 21 mg m-2 year-1. The PAH composition is dominated by parent compounds rather than alkylated homologues and is characteristic of pyrogenic sources correlating with increased motor vehicle activity and road runoff into the Tamar. There is a remarkable compositional uniformity of PAH throughout the polluted sediment core, indicating that the biogeochemical transformation and exchange processes (sorption/leaching; microbial breakdown; photo-degradation; etc.) which are known to govern the fate of experimentally-added or petroleum-derived PAH, and which exhibit compound discrimination, appear not to affect PAH in the sediments. Using a linear free energy sediment-water exchange model to simulate the repartitioning and exchange of individual PAH between the surface-mixed layer of sediment and water, we demonstrate that the current PAH concentrations in sediments are between 2 and 5 orders of magnitude greater than those expected from equilibrium partitioning with observed water concentrations. This implies that the PAH input to the sediments has been compositionally uniform and that the PAH are chemically inert. Sorptive exchange with the aqueous phase and hence the potential bioavailability of PAH appear restricted by the existence of occluded and other micro-morphologically inert forms of particle-bound PAH. PMID:3685960

  3. Oxidation of the odorous compound 2,4,6-trichloroanisole by UV activated persulfate: Kinetics, products, and pathways.

    PubMed

    Luo, Congwei; Jiang, Jin; Ma, Jun; Pang, Suyan; Liu, Yongze; Song, Yang; Guan, Chaoting; Li, Juan; Jin, Yixin; Wu, Daoji

    2016-06-01

    The transformation efficiency and products of an odorous compound 2,4,6-trichloroanisole (TCA) at the wavelength of 254 nm in the presence of persulfate were investigated for the first time. The effects of water matrix (i.e., natural organic matter (NOM), pH, carbonate/bicarbonate (HCO3(-)/CO3(2-)), and chloride ions (Cl(-))) were evaluated. The second order rate constant of TCA reacting with sulfate radical (SO4(-)) was determined to be (3.72 ± 0.10) × 10(9) M(-1) s(-1). Increasing dosage of persulfate increased the observed pseudo-first-order rate constant for TCA degradation (kobs), and the contribution of SO4(-) to TCA degradation was much higher than that of HO at each experimental condition. Degradation rate of TCA decreased with pH increasing from 4.0 to 9.0, which could be explained by the lower radical scavenging effect of dihydrogen phosphate than hydrogen phosphate in acidic condition (pH < 6). NOM significantly decreased kobs due to the effects of radical scavenging and UV absorption with the former one being dominant. kobs decreased from 2.32 × 10(-3) s(-1) to 0.92 × 10(-3) s(-1) with the CO3(2-)/HCO3(-) concentration increased from 0.5 mM to 10 mM in the UV/persulfate process, while kobs slightly decreased from 2.54 × 10(-3) s(-1) in the absence of Cl(-) to 2.10 × 10(-3) s(-1) in the presence of 10 mM Cl(-). Most of these kinetic results could be described by a steady-state kinetic model. Furthermore, liquid chromatography/electrospray ionization-triple quadrupole mass spectrometry at powerful precursor ion scan approach was used to selectively detect oxidation products of TCA. It was found that 2,4,6-trichorophenol (TCP) was the major oxidation product (i.e., the initial yield of TCP was above 90%). The second order rate constant between TCP and SO4(-) was estimated to be (4.16 ± 0.20) × 10(9) M(-1) s(-1). In addition, three products (i.e., 2,6-dichloro-1,4-benzoquinone and two aromatic ring-opening products

  4. Recent Progress in DIB Research: Survey of PAHS and DIBS

    NASA Technical Reports Server (NTRS)

    Salama, Farid; Galazutdinov, G.; Krelowski, J.; Biennier, L.; Beletsky, Y.; Song, I.

    2013-01-01

    The spectra of several neutral and ionized PAHs isolated in the gas phase at low temperature have been measured in the laboratory under experimental conditions that mimic interstellar conditions and are compared with an extensive set of astronomical spectra of reddened, early type stars [1, 2]. The comparisons of astronomical and laboratory data provide upper limits for the abundances of specific neutral PAH molecules and ions along specific lines-of-sight. Something that is not attainable from infrared observations alone. We present the characteristics of the laboratory facility (COSmIC) that was developed for this study and discuss the findings resulting from the comparison of these unique laboratory data with high resolution, high S/N ratio astronomical observations. COSmIC combines a supersonic free jet expansion with discharge plasma and high-sensitivity cavity ringdown spectroscopy and provides experimental conditions that closely mimic the interstellar conditions. The column densities of the individual neutral PAH molecules and ions probed in these surveys are derived from the comparison of these unique laboratory data with high resolution, high S/N ratio astronomical observations. The comparisons of astronomical and laboratory data lead to clear and unambiguous conclusions regarding the expected abundances for PAHs of various sizes and charge states in the interstellar environments probed in the surveys. Band profile comparisons between laboratory and astronomical spectra lead to information regarding the molecular structures and characteristics associated with the DIB carriers in the corresponding lines-of-sight. These quantitative surveys of neutral and ionized PAHs in the optical range open the way for unambiguous quantitative searches of PAHs and complex organics in a variety of interstellar and circumstellar environments.

  5. Physical model for the photo-induced toxicity of polycyclic aromatic hydrocarbons (PAHs)

    SciTech Connect

    Greenburg, B.M.; Krylov, S.N.; Huang, H.D.; Dixon, D.G.

    1994-12-31

    A model for photo-induced toxicity of PAHs to duckweed was developed. Growth inhibition was described by photochemical reactions between PAHs and a hypothetical group of biomolecules (given the notation G) which are required for growth of the plants. Light activation of PAHs was considered in a two compartment system (water and leaves). The reaction scheme includes: photooxidation of PAHs, partitioning of PAHs into leaves, triplet formation of intact PAHs, photosensitization reactions that consume G, and reaction between photooxidized PAHs and G. The assumptions used in the model are: the rate of PAH photooxidation is slower than the rate of assimilation, PAH content in solution is approximately constant over the length of the toxicity test, the fluence rate of actinic radiation is lower in the leaves than in solution, the toxicity of intact PAHs with G in the absence of light is negligible, and the reaction of photooxidized PAHs with G does not require light. The authors then analyzed a series of differential equations that described toxicity. The result was an expression for growth inhibition as a function of the initial concentration of the PAH, the spectral distribution of the light source, the absorption spectrum of the PAH, the quantum yield for formation of triplet state PAH, and the rate of photo-oxidation of the PAH. The expression also includes two complex constants that can be solved by a least squares analysis of the empirical data for growth inhibition. Thus, the model allows a prediction of PAH photo-induced toxicity using only physical parameters of PAHs.

  6. Surface plasmon resonance immunosensor for highly sensitive detection of 2,4,6-trinitrotoluene.

    PubMed

    Shankaran, Dhesingh Ravi; Gobi, K Vengatajalabathy; Sakai, Takatoshi; Matsumoto, Kiyoshi; Toko, Kiyoshi; Miura, Norio

    2005-03-15

    We have examined the sensing characteristics of a surface plasmon resonance (SPR) immunoassay for the detection of 2,4,6-trinitrotoluene (TNT) using an immunoreaction between 2,4,6-trinitrophenol-ovalbumin (TNP-OVA) conjugate and anti-2,4,6-trinitrophenol antibody (anti-TNP antibody). TNP-OVA conjugate was attached to a SPR-gold sensing surface by means of physical immobilization, which undergoes binding interaction with anti-TNP antibody. Both the immobilization and binding processes were studied from a change in the SPR-resonance angle. The quantification of TNT is based on the principle of indirect competitive immunoassay, in which the immunoreaction between the TNP-OVA conjugate and anti-TNP antibody was inhibited in the presence of free TNT in solution. The decrease in the resonance angle shift is proportional to an increase in concentration of TNT used for incubation. The immunoassay exhibited excellent sensitivity for the detection of TNT in the concentration range from 0.09 to 1000 ng/ml with good stability and reproducibility. The immunosensor developed could detect TNT as low as 0.09 ng/ml, within a response time of approximately 22 min. The sensor surface was regenerated by a brief flow of pepsin solution, which disrupts the antigen-antibody complex without destroying the conjugate biofilm. Cross-reactivity of the SPR sensor to some structurally related nitroaromatic derivative and the detection of TNT in the presence of these nitroaromatic compounds were investigated. The cross-reactivity of the SPR sensor to 2,4-dinitrotoluene (2,4-DNT), 1,3-dinitrobenzene (1,3-DNB), 2-amino-4,6-dinitrotoluene (2A-4,6-DNT) and 4-amino-2,6-dinitrotoluene (4A-2,6-DNT) were very low (< or =1.1%). The analytical characteristics of the proposed immunosensor are highly promising for the development of new field-portable sensors for on-site detection of landmines. PMID:15681190

  7. Infrared spectroscopy of matrix-isolated polycyclic aromatic hydrocarbon cations. 4. The tetracyclic PAH isomers chrysene and 1,2-benzanthracene.

    PubMed

    Hudgins, D M; Allamandola, L J

    1997-05-01

    The mid-infrared spectra of the polycyclic aromatic hydrocarbon (PAH) cations of the tetracyclic isomers chrysene (C18H12+) and 1,2-benzanthracene (C18H12+) are presented. As with previous PAH cations studied to date, the CC stretching and CH in-plane bending mode absorptions are about an order of magnitude stronger than the aromatic CH out-of-plane bending absorptions and nearly 2 orders of magnitude more intense than the corresponding bands in the neutral molecule. The CH bands arising from the out-of-plane bends in the cation are slightly weaker than the corresponding bands in the neutral species. The strongest cation bands of these species fall between 1300 and 1330 cm-1, close to the peak of the most intense interstellar emission feature in HII regions and reflection nebulae. A strong PAH cation band at slightly higher frequency than 1300 cm-1 may be associated with an asymmetric CC stretching vibration involving rings adjacent to the kink in the chain of aromatic rings. PMID:11541094

  8. Biodegradation of PAHs and PCBs in soils and sludges

    USGS Publications Warehouse

    Liu, L.; Tindall, J.A.; Friedel, M.J.

    2007-01-01

    Results from a multi-year, pilot-scale land treatment project for PAHs and PCBs biodegradation were evaluated. A mathematical model, capable of describing sorption, sequestration, and biodegradation in soil/water systems, is applied to interpret the efficacy of a sequential active-passive biotreatment process of organic chemicals on remediation sites. To account for the recalcitrance of PAHs and PCBs in soils and sludges during long-term biotreatment, this model comprises a kinetic equation for organic chemical intraparticle sequestration process. Model responses were verified by comparison to measurements of biodegradation of PAHs and PCBs in land treatment units; a favorable match was found between them. Model simulations were performed to predict on-going biodegradation behavior of PAHs and PCBs in land treatment units. Simulation results indicate that complete biostabilization will be achieved when the concentration of reversibly sorbed chemical (S RA) reduces to undetectable levels, with a certain amount of irreversibly sequestrated residual chemical (S IA) remaining within the soil particle solid phase. The residual fraction (S IA) tends to lose its original chemical and biological activity, and hence, is much less available, toxic, and mobile than the "free" compounds. Therefore, little or no PAHs and PCBs will leach from the treatment site and constitutes no threat to human health or the environment. Biotreatment of PAHs and PCBs can be terminated accordingly. Results from the pilot-scale testing data and model calculations also suggest that a significant fraction (10-30%) of high-molecular-weight PAHs and PCBs could be sequestrated and become unavailable for biodegradation. Bioavailability (large K d , i.e., slow desorption rate) is the key factor limiting the PAHs degradation. However, both bioavailability and bioactivity (K in Monod kinetics, i.e., number of microbes, nutrients, and electron acceptor, etc.) regulate PCBs biodegradation. The sequential

  9. Dust and Planetary Rings

    NASA Astrophysics Data System (ADS)

    Siddiqui, Muddassir

    ABSTRACT Space is not empty it has comic radiations (CMBR), dust etc. Cosmic dust is that type of dust which is composed of particles in space which vary from few molecules to 0.1micro metres in size. This type of dust is made up of heavier atoms born in the heart of stars and supernova. Mainly it contains dust grains and when these dust grains starts compacting then it turns to dense clouds, planetary ring dust and circumstellar dust. Dust grains are mainly silicate particles. Dust plays a major role in our solar system, for example in zodiacal light, Saturn's B ring spokes, planetary rings at Jovian planets and comets. Observations and measurements of cosmic dust in different regions of universe provide an important insight into the Universe's recycling processes. Astronomers consider dust in its most recycled state. Cosmic dust have radiative properties by which they can be detected. Cosmic dusts are classified as intergalactic dusts, interstellar dusts and planetary rings. A planetary ring is a ring of cosmic dust and other small particles orbiting around a planet in flat disc shape. All of the Jovian planets in our solar system have rings. But the most notable one is the Saturn's ring which is the brightest one. In March 2008 a report suggested that the Saturn's moon Rhea may have its own tenuous ring system. The ring swirling around Saturn consists of chunks of ice and dust. Most rings were thought to be unstable and to dissipate over course of tens or hundreds of millions of years but it now appears that Saturn's rings might be older than that. The dust particles in the ring collide with each other and are subjected to forces other than gravity of its own planet. Such collisions and extra forces tend to spread out the rings. Pluto is not known to have any ring system but some Astronomers believe that New Horizons probe might find a ring system when it visits in 2015.It is also predicted that Phobos, a moon of Mars will break up and form into a planetary ring

  10. Traceable Ring Signature

    NASA Astrophysics Data System (ADS)

    Fujisaki, Eiichiro; Suzuki, Koutarou

    The ring signature allows a signer to leak secrets anonymously, without the risk of identity escrow. At the same time, the ring signature provides great flexibility: No group manager, no special setup, and the dynamics of group choice. The ring signature is, however, vulnerable to malicious or irresponsible signers in some applications, because of its anonymity. In this paper, we propose a traceable ring signature scheme. A traceable ring scheme is a ring signature except that it can restrict “excessive” anonymity. The traceable ring signature has a tag that consists of a list of ring members and an issue that refers to, for instance, a social affair or an election. A ring member can make any signed but anonymous opinion regarding the issue, but only once (per tag). If the member submits another signed opinion, possibly pretending to be another person who supports the first opinion, the identity of the member is immediately revealed. If the member submits the same opinion, for instance, voting “yes” regarding the same issue twice, everyone can see that these two are linked. The traceable ring signature can suit to many applications, such as an anonymous voting on a BBS. We formalize the security definitions for this primitive and show an efficient and simple construction in the random oracle model.

  11. Sunset on Saturn's Rings

    NASA Technical Reports Server (NTRS)

    1996-01-01

    This is a rare view of Saturn's rings seen just after the Sun has set below the ring plane, taken with the Hubble Space Telescope on Nov. 21, 1995.

    This perspective is unusual because the Earth is slightly above (2.7 degrees latitude) Saturn's rings and the Sun is below them. Normally we see the rings fully illuminated by the Sun.

    The photograph shows three bright ring features: the F Ring, the Cassini Division, and the C Ring (moving from the outer rings to the inner). The low concentration of material in these rings allows light from the Sun to shine through them. The A and B rings are much denser, which limits the amount of light that penetrates through them. Instead, they are faintly visible because they reflect light from Saturn's disk.

    Scientists believe that the F Ring is slightly warped because it disappears part way around on the right (West) side. Hubble's high resolution shows the that A Ring's shadow obscures part of the F ring (right).

    The image was assembled from 20 exposures taken with Wide Field Planetary Camera-2 over 8 hours.

    The Wide Field/Planetary Camera 2 was developed by the Jet Propulsion Laboratory and managed by the Goddard Spaced Flight Center for NASA's Office of Space Science.

    This image and other images and data received from the Hubble Space Telescope are posted on the World Wide Web on the Space Telescope Science Institute home page at URL http://oposite.stsci.edu/pubinfo/

  12. Distribution of persistent organic pollutants (PAHs, Me-PAHs, PCBs) in dissolved, particulate and sedimentary phases in freshwater systems.

    PubMed

    Rabodonirina, Suzanah; Net, Sopheak; Ouddane, Baghdad; Merhaby, Dima; Dumoulin, David; Popescu, Tudor; Ravelonandro, Pierre

    2015-11-01

    The occurrence of three groups of hazardous organic contaminants (PCBs, PAHs, Me-PAHs) in fifteen watercourses and rivers located in highly urbanized and industrialized zones was studied. The distribution of 62 organic contaminants was determined in three matrices: in the dissolved phase, associated with suspended solid matter (SSM) and in sediment. Their distributions in the aquatic environment depend strongly on their physicochemical properties. Low molecular weight PAHs were predominant in the dissolved phase while those with high molecular weight accumulated preferentially in SSM and sediments. Among the 28 PCBs congeners, only PCB153 was detected. The results showed that the contamination of these areas originated mainly from combustion processes. The three the most polluted sites identified are surrounded by big cities. Ecotoxicological assessment based on the international Sediment Quality Guidelines (SQGs) showed that the toxic effects of the sediment in these watercourses and rivers occurred due to high levels of hydrocarbons. PMID:26142749

  13. Pseudomonas sp. CL7 from Sludge Removed 2,3,4,6-Tetrachlorophenol in Vivo and in Vitro Condition.

    PubMed

    Karn, Santosh Kumar; Reddy, M Sudhakara; Chakrabarti, Swapan Kumar

    2016-04-01

    The present research focused on 2,3,4,6-Tetrachlorophenol (2,3,4,6-TeCP) mineralizing bacterium from the sludge of pulp and paper industry and identified as Pseudomonas sp. CL7 by 16s rRNA gene sequences analysis. This isolate degraded 2,3,4,6-TeCP as indicated by stoichiometric release of chloride and biomass formation. High pressure liquid chromatography (HPLC) analysis showed that Pseudomonas sp. (CL7) was able to mineralize a higher concentration of 2,3,4,6-TeCP (600 mg/l or 2.5 mM) than any previously reported 2,3,4,6-TeCP degrading bacteria. As the concentration of 2,3,4,6-TeCP increased from 50 (0.21 mM) to 600 mg/l (2.5 mM), the reduction in the cell growth was observed and the 2,3,4,6-TeCP degradation was more than 85% in all the concentrations in the present study. CL7 was able to remove 100% of 2,3,4,6-TeCP from the sludge (in Vitro condition) when supplemented with 100 mg/l (0.42 mM) of 2,3,4,6-TeCP and grown for two weeks. This study showed that CL7 can be used for bioremediation of 2,3,4,6-TeCP. PMID:27131053

  14. Quantification of PAHs and oxy-PAHs on airborne particulate matter in Chiang Mai, Thailand, using gas chromatography high resolution mass spectrometry

    NASA Astrophysics Data System (ADS)

    Walgraeve, Christophe; Chantara, Somporn; Sopajaree, Khajornsak; De Wispelaere, Patrick; Demeestere, Kristof; Van Langenhove, Herman

    2015-04-01

    An analytical method using gas chromatography high resolution mass spectrometry was developed for the determination of 16 polycyclic aromatic hydrocarbons (PAHs) and 12 oxygenated PAHs (of which 4 diketones, 3 ketones, 4 aldehydes and one anhydride) on atmospheric particulate matter with an aerodynamic diameter less than 10 μm (PM10). The magnetic sector mass spectrometer was run in multiple ion detection mode (MID) with a mass resolution above 10 000 (10% valley definition) and allows for a selective accurate mass detection of the characteristic ions of the target analytes. Instrumental detection limits between 0.04 pg and 1.34 pg were obtained for the PAHs, whereas for the oxy-PAHs they ranged between 0.08 pg and 2.13 pg. Pressurized liquid extraction using dichloromethane was evaluated and excellent recoveries ranging between 87% and 98% for the PAHs and between 74% and 110% for 10 oxy-PAHs were obtained, when the optimum extraction temperature of 150 °C was applied. The developed method was finally used to determine PAHs and oxy-PAHs concentration levels from particulate matter samples collected in the wet season at 4 different locations in Chiang Mai, Thailand (n = 72). This study brings forward the first concentration levels of oxy-PAHs in Thailand. The median of the sum of the PAHs and oxy-PAHs concentrations was 3.4 ng/m3 and 1.1 ng/m3 respectively, which shows the importance of the group of the oxy-PAHs as PM10 constituents. High molecular weight PAHs contributed the most to the ∑PAHs. For example, benzo[ghi]perylene was responsible for 30-44% of the ∑PAHs. The highest contribution to ∑oxy-PAHs came from 1,8-napthalic anhydride (26-78%), followed by anthracene-9,10-dione (4-27%) and 7H-benzo[de]anthracene-7-one (6-26%). Indications of the degradation of PAHs and/or formation of oxy-PAHs were observed.

  15. BIODEGRADATION OF SEDIMENT-BOUND PAHS IN FIELD-CONTAMINATED SEDIMENT

    EPA Science Inventory

    The biodegradation of polycyclic aromatic hydrocarbons (PAHs) has been reported to occur under aerobic, sulfate reducing, and denitrifying conditions. PAHs present in contaminated sites, however, are known for their persistence. Most published studies were conducted in systems wh...

  16. Increased zooplankton PAH concentrations across hydrographic fronts in the East China Sea.

    PubMed

    Hung, Chin-Chang; Ko, Fung-Chi; Gong, Gwo-Ching; Chen, Kuo-Shu; Wu, Jian-Ming; Chiang, Hsin-Lun; Peng, Sen-Chueh; Santschi, Peter H

    2014-06-15

    The Changjiang has transported large quantities of polycyclic aromatic hydrocarbons (PAHs) to the East China Sea (ECS), but information of these pollutants in zooplankton is limited. To understand PAHs pollution in zooplankton in the ECS, total concentrations of PAHs in zooplankton from surface waters were measured. Values of PAHs ranged from 2 to 3500 ng m(-3) in the ECS, with highest PAHs levels located at the salinity front between the Changjiang Diluted Water (CDW) and the mid-shelf waters. In contrast, concentrations of zooplankton PAHs in the mid-shelf and outer-shelf waters were significantly lower (2-23 ng m(-3)) than those in the CDW. These results demonstrate that PAHs are conspicuously accumulated in zooplankton at the salinity front between the CDW and the mid-shelf waters. These higher levels of PAHs in zooplankton at the salinity front may be further biomagnified in marine organisms of higher trophic levels through their feeding activities. PMID:24775063

  17. RISKS TO FISH AND OTHER AQUATIC ORGANISMS FROM PAHS IN NATURAL SYSTEMS

    EPA Science Inventory

    Assessing the risks of PAHs to aquatic organisms requires consideration of several factors. First, environmental PAH concentrations must be characterized, including chemical partitioning information important to bioavailability. Second, UV radiation exposures must be evaluated re...

  18. 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. PMID:24981104

  19. Coal-tar pavement sealants might substantially increase children's PAH exposures

    USGS Publications Warehouse

    Williams, E. Spencer; Mahler, Barbara J.; Van Metre, Peter C.

    2012-01-01

    Dietary ingestion has been identified repeatedly as the primary route of human exposure to polycyclic aromatic hydrocarbons (PAHs), seven of which are classified as probable human carcinogens (B2 PAHs) by the U.S. EPA. Humans are exposed to PAHs through ingestion of cooked and uncooked foods, incidental ingestion of soil and dust, inhalation of ambient air, and absorption through skin. Although PAH sources are ubiquitous in the environment, one recently identified PAH source stands out: Coal-tar-based pavement sealant—a product applied to many parking lots, driveways, and even playgrounds primarily in the central, southern, and eastern U.S.—has PAH concentrations 100–1000 times greater than most other PAH sources. It was reported recently that PAH concentrations in house dust in residences adjacent to parking lots with coal-tar-based sealant were 25 times higher than in residences adjacent to unsealed asphalt parking lots.

  20. 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...