Detailed Information on Publication Record
2003
Photodegradation of Polycyclic Aromatic Hydrocarbons and Nitrated Polycyclic Aromatic Hydrocarbons in Dichlormethane and Isooctane Solution
CVRČKOVÁ, Olga, Miroslav CIGANEK, Jana BLATOVÁ and Zdeněk ŠIMEKBasic information
Original name
Photodegradation of Polycyclic Aromatic Hydrocarbons and Nitrated Polycyclic Aromatic Hydrocarbons in Dichlormethane and Isooctane Solution
Name in Czech
Fotodegradace PAH a nitrovaných PAH
Authors
CVRČKOVÁ, Olga (203 Czech Republic), Miroslav CIGANEK (203 Czech Republic), Jana BLATOVÁ (203 Czech Republic) and Zdeněk ŠIMEK (203 Czech Republic, guarantor)
Edition
Zurich, Switzerland, SACH Conference. Analytical Chemistry of Organic Contaminants in the Enwironment, p. 45-45, 1 pp. 2003
Publisher
SACH Conference. Analytical Chemistry of Organic Contaminants in the Enwironment
Other information
Language
English
Type of outcome
Stať ve sborníku
Field of Study
10406 Analytical chemistry
Country of publisher
Switzerland
Confidentiality degree
není předmětem státního či obchodního tajemství
Organization unit
Faculty of Science
Keywords in English
Photodegradation; Polycyclic Aromatic Hydrocarbons; Nitrated Polycyclic Aromatic Hydrocarbons;
Změněno: 31/1/2006 16:00, doc. RNDr. Zdeněk Šimek, CSc.
Abstract
V originále
Photodegradation of two PAHs (anthracene and chrysene), two NPAHs (9-nitroanthracene, and 6-nitrochrysene) and seven MePAHs (1-methylchrysene, 2-methylchrysene, 3-methylchrysene, 4-methylchrysene 5-methylchrysene, 6-methylchrysene, 1-methylantracene, -methylantracene, 9-methylantracene) was studied in isooctane solutions exposed to the UV radiation from light simulator. Samples were placed in closed glass vials. PAHs and NPAHs were divided into three groups according to their life times. Degradation of all PAHs and NPAHs was faster in dichloromethane compared with isooctane. Decomposition of NPAHs was easier than degradation of corresponding parent PAHs. The most frequent photoproducts were quinone, benzoic acid and derivatives with hydroxyl, carbonyl and carboxyl groups for both PAHs and NPAHs. Chlorinated compounds were identified in dichloromethane. Degradation intermediates underwent further oxidation, fragmentation, reduction or radical chlorine addition in dichloromethane. Final degradation products of all PAHs were n-alcanes. Based on GC-MS data the mechanism of photoproducts formation was proposed.
Links
GA525/03/0367, research and development project |
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