Extraction of low molecular weight polynuclear aromatic hydrocarbons from ashes of coal-operated power plants

1987 ◽  
Vol 59 (17) ◽  
pp. 2066-2069 ◽  
Author(s):  
Filippo. Mangani ◽  
Achille. Cappiello ◽  
Giancarlo. Crescentini ◽  
Fabrizio. Bruner ◽  
Loretta. Bonfanti
Keyword(s):  
Molecular Weight ◽  
Aromatic Hydrocarbons ◽  
Power Plants ◽  
Polynuclear Aromatic Hydrocarbons ◽  
Low Molecular Weight

Methods for the Synthesis of Polyethereketone

2018 ◽  
Vol 935 ◽  
pp. 27-30
Author(s):  
K.T. Shakhmurzova ◽  
Zh.I. Kurdanova ◽  
Arthur E. Baikaziev ◽  
Karina Kh. Teunova ◽  
Azamat A. Zhansitov ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Aromatic Hydrocarbons ◽  
Electrophilic Substitution ◽  
Methylene Chloride ◽  
Dicarboxylic Acids ◽  
Polynuclear Aromatic Hydrocarbons ◽  
Low Molecular Weight ◽  
Monocarboxylic Acids ◽  
Synthesis Time ◽  
Aromatic Dicarboxylic Acids

The data on the methods for the preparation of polyetherketones by electrophilic and nucleophilic methods are considered and generalized. It is shown that polyetherketones by electrophilic substitution are carried out as homopolycondensation aromatic monocarboxylic acids and their halides and polycondensation of polynuclear aromatic hydrocarbons with aromatic dicarboxylic acids or their halides, and phosgene in organic solvents (1,2-dichloroethane, methylene chloride, nitrobenzene and etc.) in the presence of Ziegler-Natt catalysts. However, this process has not found an industrial application in view of such disadvantages as low yield of the desired product, the formation of a polymer with low molecular weight, synthesis time (15-40 hours), the use of large amounts of catalyst, the complexity of polymer purification of it.

scholarly journals Effect of WC/Ni–Cr additive on changes in the composition of an atmospheric residue in the course of cracking

2019 ◽  
Vol 17 (2) ◽  
pp. 499-508 ◽  
Author(s):  
Galina S. Pevneva ◽  
Natalya G. Voronetskaya ◽  
Nikita N. Sviridenko ◽  
Anatoly K. Golovko
Keyword(s):  
Molecular Weight ◽  
Tungsten Carbide ◽  
Aromatic Hydrocarbons ◽  
Aromatic Compounds ◽  
Low Molecular Weight ◽  
Nickel Chromium ◽  
Atmospheric Residue ◽  
Sulfur Containing ◽  
Catalytic Additive ◽  
Sulfur Containing Compounds

AbstractThe paper presents the results of investigation of changes in the composition of hydrocarbons and sulfur-containing compounds of an atmospheric residue in the course of cracking in the presence of a tungsten carbide–nickel–chromium (WC/Ni–Cr) catalytic additive and without it. The cracking is carried out in an autoclave at 500 °C for 30 min. The addition of the WC/Ni–Cr additive promotes the deepening of reactions of destruction not only of resins and asphaltenes, but also high molecular weight naphthene-aromatic compounds of the atmospheric residue. It is shown that the content of low molecular weight C9–C17 n-alkanes and C9–C10 alkylbenzenes rose sharply in the products of cracking with addition of WC/Ni–Cr in comparison with those produced without the additive. Alkyl- and naphthene-substituted aromatic hydrocarbons of benzene, naphthalene, phenanthrene series, polyarenes, benzo- and dibenzothiophenes are identified.

scholarly journals The ldentification of High Molecular Weight Polynuclear Aromatic Hydrocarbons in a Biologically Active Fraction of Cigarette Smoke Condensate

1977 ◽  
Vol 9 (2) ◽  
Author(s):  
M.E. Snook ◽  
R.F. Severson ◽  
R.F. Arrendale ◽  
H.C. Higman ◽  
O.T. Chortyk
Keyword(s):  
Molecular Weight ◽  
High Molecular Weight ◽  
Cigarette Smoke ◽  
Aromatic Hydrocarbons ◽  
Polynuclear Aromatic Hydrocarbons ◽  
Biologically Active ◽  
Retention Data ◽  
Active Fraction ◽  
Cigarette Smoke Condensate ◽  
Preparative Gas Chromatography

AbstractA gel filtration chromatography method was developed for the isolation and concentration of the high molecular weight polynuclear aromatic hydrocarbons (PAH) contained in the most biologically active fraction of cigarette smoke condensate (CSC). The unusually complex mixture of large PAH found in CSC necessitated the use of preparative gas chromatography followed by high-pressure liquid chromatography to achieve separation and identification. Mass spectral, ultra-violet absorption, and chromatographic retention data were needed for the comprehensive identification of the large molecular weight PAH components of CSC. The majority of the more than 200 isolated compounds were identified. Compounds newly identified in CSC included 3,4-dimethylenepyrene, 3,4-trimethylenepyrene, cyclopenta(c,-d)pyrene, 4,5-methylenetriphenylene, benzo[b]perylene, and several dibenzofluoranthenes.

scholarly journals Correlation of Polynuclear Aromatic Hydrocarbon Formation Between Pyrolysis and Smoking

1977 ◽  
Vol 9 (1) ◽  
Author(s):  
R. F. Severson ◽  
W. S. Schlotzhauer ◽  
R. F. Arrendale ◽  
M. E. Snook ◽  
H. C. Higman
Keyword(s):  
Molecular Weight ◽  
Aromatic Hydrocarbon ◽  
Petroleum Ether ◽  
High Molecular Weight ◽  
Cigarette Smoke ◽  
Aromatic Hydrocarbons ◽  
Polynuclear Aromatic Hydrocarbons ◽  
Polynuclear Aromatic Hydrocarbon ◽  
Cigarette Smoke Condensate ◽  
Hydrocarbon Formation

AbstractTobacco, its petroleum ether (PE) extract, and the residual extracted tobacco (marc) were pyrolyzed at 650-750°C, 650-850°C, and 700°C, respectively. Analyses of the polynuclear aromatic hydrocarbons (PAH) produced showed that the pyrolysis of the tobacco and the PE extract at 700°C produced PAH profiles comparable to those found in cigarette smoke condensate (CSC). The data indicated that most of the alkyl PAH and the major PAH in cigarette smoke are derived from the PE extractables of tobacco. The constituents of the marc were the major precursors for phenols, oxygenated PAH, and Iow molecular weight acids; and those of PE extract were the major producers of high molecular weight acids.

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