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Beyond the 16 EPA priority pollutant PAHs : environmental characterizations of oxygenated PAHs and dibenzopyrene isomers /Layshock, Julie. January 1900 (has links)
Thesis (Ph. D.)--Oregon State University, 2010. / Printout. Includes bibliographical references (leaves 104-108). Also available on the World Wide Web.
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Mechanistic studies on the thermal cyclodehydrogenations of polycyclic aromatic hydrocarbonsXue, Xiang January 2008 (has links)
Thesis advisor: Lawrence T. Scott / Thermal cyclodehydrogenation is the key step in the total synthesis of fullerene C60 and represents an important family of carbon-carbon bond-forming reactions. My research focuses on understanding the mechanism of C-C bond formation in the high temperature cyclodehydrogenations of PAHs using appropriate test cases to form 5- or 6-membered rings. My goal was to understand more about molecular reactions under extreme conditions and thereby realize new synthetic pathways for new molecules. This dissertation describes the synthesis of several substrates and studies of their thermal cyclodehydrogenations. Chapter 1 presents the cyclodehydrogenations of [5]helicene and benzo[5]helicene to form 6-membered rings under flash vacuum pyrolysis (FVP) conditions. An observed rate difference established that an electrocyclic mechanism is favored in this case and disproved the radical cyclization and 1,2-hydrogen shift/carbene insertion mechanisms. Chapter 2 describes the cyclodehydrogenations of phenyl-substituted phenanthrenes to form 6-membered rings under FVP conditions. The radical mechanism is ruled out because of the rate difference. Chapter 3 shows the synthesis of 7-(9H-fluoren-9-ylidene)-7H-benzo[c]fluorene and its thermal cyclodehydrogenation to form 6-membered rings under FVP conditions. In chapter 4, the cyclodehydrogenations of phenyl-substituted anthracenes and phenanthrenes to form 5-membered rings under FVP conditions are presented. The unexpected dominance of phenyl loss suggests that radical mechanisms are occurring during the cyclodehydrogenations. Chapter 5 describes the cyclodehydrogenations of [4]helicene and benzo[4]helicene to form 5-membered rings under FVP conditions. The results point to a carbene cyclization mechanism, in competition with the radical mechanism. / Thesis (PhD) — Boston College, 2008. / Submitted to: Boston College. Graduate School of Arts and Sciences. / Discipline: Chemistry.
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Modification, development and application of extraction methods for PAHs in sediments and waterSibiya, Precious Nokwethemba 14 February 2013 (has links)
Polycyclic aromatic hydrocarbons (PAHs) are an important class of persistent organic pollutants (POPs) that are commonly found in the environment at low concentrations. POPs are long-lived organic compounds and originate almost entirely from anthropogenic activities such as chemical industries, combustion and agriculture activities. Owing to their potential carcinogenicity, mutagenicity and teratogenicity, PAHs have been determined in several matrices, particularly water, soil and sediment. Hazards associated with these compounds are owing to their hydrophobic character, persistence and bioaccumulation properties of several individual PAHs. Hence the primary goal of this research was to identify and determine PAHs in water and sediment samples, from rivers and dams in greater Johannesburg area, South Africa.
In this work, three extraction techniques have been optimized for the extraction of PAHs in various samples. The extraction techniques based on hollow fiber liquid phase microextraction (HF-LPME) and solid phase extraction (SPE) were optimized for aqueous samples. Microwave assisted extraction technique (MAE) was optimized for solid samples. The optimized methods were applied to real water and sediment samples in and around Johannesburg area. HF-LPME and SPE techniques were compared with each other, while MAE was compared with Soxhlet (SE) in terms of their extraction efficiencies, enrichment factors, detection limits, relative standard deviations and concentrations of PAHs found in real samples.
HF-LPME technique involved extraction of PAHs from a 20 mL sample containing 20% acetonitrile as a modifier. The PAHs were extracted into a 5 cm hollow fibre filled with heptane as organic solvent. At a stirring speed and extraction time of 600 rpm and 30 minutes, respectively, the acceptor solvent was collected to be analysed by GC-MS. The obtained enrichment factors ranged from 40 to 95 and the recoveries ranged from 3-8% depending on individual PAHs. The detection limits ranged from 23.0-95.0 ng L-1 while relative standard deviations for the recoveries were less than 5%, (n=3). The concentrations obtained in real water samples ranged from 30.3-213.8 ng L-1 and the relative standard deviations were between 0.8-11.9%, (n=3). SPE technique involved extraction of PAHs from a 100 mL sample containing 10% methanol as a modifier. The PAHs were extracted using C18 cartridges with 40% methanol in water as conditioning solvents and 3 mL acetone: THF (1:1) as eluting solvents. After eluting, the analyte is reduced to 1 mL under nitrogen and then analysed using GC-MS. The obtained enrichment factors ranged from 78-135 depending on the individual PAH. The detection limits ranged from 20.0-52.0 ng L-1. The relative standard deviations for the obtained enrichment factors were less than 6%. The obtained concentrations from real water samples ranged from 21.4-615.7 ng L-1 and the relative standard deviations were between 1.9-13.0%, (n=3).
In MAE technique, the extraction was carried out with 20 mL of hexane: acetone (1:1, v/v) mixture with 1 g sample at 250 W for 20 minutes. After extraction, the extract was cleaned and reduced to 1 mL under nitrogen and then injected into an HPLC-Fluoresence system. The obtained recoveries ranged from 61-98% depending on the individual PAHs. The detection limits obtained ranged from 0.03-0.5 μg L-1 for HPLC-Fluorescence. The relative standard deviations were less than 6% for the obtained enrichment factors. The obtained concentrations in the sediments ranged from 61-45281μg kg-1 and the relative standard deviations ranged from 2.1-10.8%, (n=3).
The possible major sources of PAHs pollution in rivers and dams in great Johannesburg area was suspected to be due to poor wastewater and solid waste management in informal settlements and a large oil spill accident that happened. This is supported by the large concentrations of PAHs found in sediments from Jukskei River which passes through one of the largest informal settlements. The pH in this river is also basic with large conductivity suggesting the presence of anions. The recipient dam of this river had also problems of algae and weeds growing in it. The influence of oil spill that happened is supported by decreasing concentrations of PAHs in the sediments with distance away from the accident area in the Blaauwpan dam. Other possible sources of PAHs are vehicle emission since studies have shown that from about 2005, the number of these in high ways in the city have been increasing by about 15-20% per year.
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Effects of benzo[a]pyrene on the biological function of eosinophilsGu, Jie 01 January 2011 (has links)
No description available.
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Examination of selective quenching agents for polycyclic aromatic hydrocarbons in polyamido amine dendrimers /Wade, Deborah A. January 2000 (has links)
Thesis (Ph. D.)--University of Missouri-Columbia, 2000. / Typescript. Vita. Includes bibliographical references. Also available on the Internet.
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Examination of selective quenching agents for polycyclic aromatic hydrocarbons in polyamido amine dendrimersWade, Deborah A. January 2000 (has links)
Thesis (Ph. D.)--University of Missouri-Columbia, 2000. / Typescript. Vita. Includes bibliographical references. Also available on the Internet.
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Synthesis of derivatives of 4H-cyclopenta[def]phenanthren-4-one and development of synthetic strategies for the polycyclic aromatic hydrocarbons with carbon frameworks represented on the surface of C₆₀Han, Xiaoqing. January 2001 (has links)
Thesis (M.S.)--West Virginia University, 2001. / Title from document title page. Document formatted into pages; contains ix, 41 p. : ill. Includes abstract. Includes bibliographical references (p. 39-41).
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Part I, Synthetic approaches to borepin ; Part II, Reactions in the dihydroethanoanthracene seriesShenoy, Purushotham K., 1933- January 1966 (has links)
No description available.
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Modelling interactions of polycyclic aromatic hydrocarbons during soot formationTotton, Timothy Stephen January 2012 (has links)
No description available.
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The effects of 3-methylcholanthrene, benz(a)anthracene, and anthracene on Friend virus leukemiaChery, Marsha Parkinson, 1942- January 1968 (has links)
No description available.
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