2003
Photodegradation of Polycyclic Aromatic Hydrocarbons and Nitrated Polycyclic Aromatic Hydrocarbons in Dichlormethane and Isooctane Solution
CVRČKOVÁ, Olga; Miroslav CIGANEK; Jana BLATOVÁ a Zdeněk ŠIMEKZákladní údaje
Originální název
Photodegradation of Polycyclic Aromatic Hydrocarbons and Nitrated Polycyclic Aromatic Hydrocarbons in Dichlormethane and Isooctane Solution
Název česky
Fotodegradace PAH a nitrovaných PAH
Autoři
CVRČKOVÁ, Olga; Miroslav CIGANEK; Jana BLATOVÁ a Zdeněk ŠIMEK
Vydání
Zurich, Switzerland, SACH Conference. Analytical Chemistry of Organic Contaminants in the Enwironment, od s. 45-45, 1 s. 2003
Nakladatel
SACH Conference. Analytical Chemistry of Organic Contaminants in the Enwironment
Další údaje
Jazyk
angličtina
Typ výsledku
Stať ve sborníku
Obor
10406 Analytical chemistry
Stát vydavatele
Švýcarsko
Utajení
není předmětem státního či obchodního tajemství
Označené pro přenos do RIV
Ano
Organizační jednotka
Přírodovědecká fakulta
Klíčová slova anglicky
Photodegradation; Polycyclic Aromatic Hydrocarbons; Nitrated Polycyclic Aromatic Hydrocarbons;
Štítky
Změněno: 31. 1. 2006 16:00, doc. RNDr. Zdeněk Šimek, CSc.
Anotace
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.
Návaznosti
| GA525/03/0367, projekt VaV |
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