Aromaticity polyaromatic hydrocarbons

The vast majority of aromatic compounds have a closed loop of six electrons in a ring (the aromatic sextet), and we consider these compounds first. It is noted that a formula periodic table for the benzenoid polyaromatic hydrocarbons has been developed. ... 

Bayer, U. 1978. In vivo induction of sister chromatid exchanges by three polyaromatic hydrocarbons. Pages 42428 in P.W. Jones and R.I. Freudenthal (eds.) Carcinogenesis — A Comprehensive Survey. Vol. 3. Polynuclear Aromatic Hydrocarbons Second International Symposium on Analysis, Chemistry, and Biology. Raven Press, New York. 

Melius, P., D. Elam, M. Kilgore, B. Tan, and W.P. Schoor. 1980. Mixed function oxidase inducibility and polyaromatic hydrocarbon metabolism in the mullet, sea catfish, and Gulf killifish. Pages 1059-1075 in A. Bjorseth and A.J. Dennis (eds.). Polynuclear Aromatic Hydrocarbons Chemistry and Biological Effects. Battelle Press, Columbus, OH. 

Spectrofluorimetric methods are applicable to the determination of aliphatic hydrocarbons, and humic and fulvic acids in soil, aliphatic hydrocarbons polyaromatic hydrocarbons, optical whiteners, and selenium in non-saline sediments, aliphatic aromatic and polyaromatic hydrocarbons and humic and fulvic acids in saline sediments. The only application found in luminescence spectroscopy is the determination of polychlorobiphenyl in soil. Generally speaking, concentrations down to the picogram (pg L 1), level can be determined by this technique with recovery efficiencies near f00%. 

Aliphatic hydrocarbons, triazine, substituted urea type and phenoxyacetic acid types of herbicides, Fluazifop and Fluazifop-butyl herbicides, ethylene diamine tetracetic acid salts in soil, aliphatic and polyaromatic hydrocarbons, phthalate esters, various organosulphur compounds, triazine herbicides, optical whiteners, mixtures of organic compounds and organotin compounds in non-saline sediments, aromatic hydrocarbons, humic and fulvic acids and mixtures of organic compounds in saline sediments and non-ionic surfactants and cobalamin in sludges. 

For more volatile compounds in soils, such as aromatic hydrocarbons, alcohols, aldehydes, ketones, chloroaliphatic hydrocarbons, haloaromatic hydrocarbons, acetonitrile, acrylonitrile and mixtures of organic compounds a combination of gas chromatography with purge and trap analysis is extremely useful. Pyrolysis gas chromatography has also found several applications, heteroaromatic hydrocarbons, polyaromatic hydrocarbons, polymers and haloaromatic compounds and this technique has been coupled with mass spectrometry, (aliphatic and aromatic hydrocarbons and mixtures of organic compounds). 

Thomas etal. [72] used pyrolysis gas chromatography-mass spectrometry as a fast economic screening technique for polyaromatic hydrocarbons. Thomas used reverse-phase liquid chromatography with atmospheric pressure chemical ionization mass spectrometry/mass spectrometry for the determination of polycyclic aromatic sulphur heterocycles in sediments. 

The marine environment acts as a sink for a large proportion of polyaromatic hydrocarbons (PAH) and these compounds have become a major area of interest in aquatic toxicology. Mixed function oxidases (MFO) are a class of microsomal enzymes involved in oxidative transformation, the primary biochemical process in hydrocarbon detoxification as well as mutagen-carcinogen activation (1,2). The reactions carried out by these enzymes are mediated by multiple forms of cytochrome P-450 which controls the substrate specificity of the system (3). One class of MFO, the aromatic hydrocarbon hydroxylases (AHH), has received considerable attention in relation to their role in hydrocarbon hydroxylation. AHH are found in various species of fish (4) and although limited data is available it appears that these enzymes may be present in a variety of aquatic animals (5,6,7,8). 

Polyaromatic hydrocarbons (PAH) are those which exists as combined aromatic ring structures represented by naphthalene (C10Hg) ... 

Physical Form, brown to black oily liquid new mineral-based crankcase oil contains petrochemicals (straight-chain hydrocarbons, aromatic hydrocarbons, and polyaromatic hydrocarbons or PAH) plus stabilizers and detergents including zinc dithiophosphate, zinc diaryl or dialkyl dithiophosphates (ZTDP), calcium alkyl phenates, magnesium, sodium, and calcium sulfonates, tricresyl phosphates, molybdenum disulfide, heavy metal soaps, cadmium, and zinc. ... 

The hydrocarbons in cmde oil are alkanes, olefins, aromatics, polyaromatics, and organic compounds containing S, N, 0, and heavy metals. Since there are many isomers of aU of these types of molecules, the reactions implied by the preceding equations rapidly approach infinity. A representative reaction of these might be the cracking of hexadecane (number 3 heating oil) into octane and octette (components in gasoline). 

According to the vendor, this technology is capable of removing chlorinated hydrocarbons, aliphatic hydrocarbons, aromatics, benzene, toluene, xylene, carbon tetrachloride, vinyl chloride, dichloromethane, and trichloroethane. Polychlorinated biphenyls (PCBs), polyaromatic hydrocarbons (PAHs), and volatile inorganic solvents can also be removed. The technology is currently in use and is commercially available. 

Another consequence of increased reaction temperatures is the shift in the equilibrium concentrations of polyaromatic hydrocarbons and their hydrogenated derivatives. At high temperatures, the fully aromatic hydrocarbons are thermodynamically favored, especially at the pressures of today s HDS reactors. As the concentration of polyaromatics increases, the fluorescence of the finished fuel increases. This may cause problems with other specifications, as discussed shortly. 

Many polycyclic aromatic amines and aldehydes are commercially available, but their supply is very limited. Preparation of these starting materials is necessary for studying the (3-lactam formation reaction [93]. Nitro compounds are the precursors for the amines. An important task was to prepare polycyclic aromatic nitro compounds, particularly those of chrysene, phenanthrene, pyrene, and dibenzofluorene in good yield. Nitration of these hydrocarbons with concentrated nitric acid in sulfuric acid is a widely used reaction for this purpose. Our research culminated in facile synthesis of polyaromatic nitro derivative 9 starting from polyaromatic hydrocarbons (PAHs) 8 through the use of bismuth nitrate impregnated with clay (Scheme 1) ([94, 95] for some examples of bismuth nitrate-catalyzed reactions... 

From the selectivity point of view, LC-NMR coupling is especially suited to the analysis of compound classes such as nitroaromatics, phenols, aromatic amines, aromatic carboxylic acids, polyaromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), and azo- and anthraquinone dyes. Another advantage of LC-NMR coupling for the investigation of aromatic compounds in environmental samples is that the position of substituents on the aromatic ring, e.g. in unknown metabolites or degradation products, can best be determined by NMR spectroscopy. 

Polycyclic aromatic hydrocarbons represent a class of compounds of great environmental concern due to their suspected mutagenic and carcinogenic properties [42-47]. Unease over the potential adverse health effects of polycyclic aromatic hydrocarbons is evident in the recent inclusion of P6 polyaromatic hydrocarbons in the Environmental Protection Agency s priority contaminates list. Polycyclic aromatic hydrocarbon contaminates pose several potential health risks due to the persistence of these compounds in the environment [48,49], their tendency to strongly bind to soil surfaces [50-52], and their presence in a wide variety of common media (air, dust, soil and food) [53]. Possible risks are associated with skin contact, inhalation or ingestion of contaminated dust, soil, or air, and ingestion of contaminated food. 

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