Oxidation of aromatic and aliphatic hydrocarbons by OH radicals photochemically generated from H2O2 in ice
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F06%3A00016117" target="_blank" >RIV/00216224:14310/06:00016117 - isvavai.cz</a>
Alternative codes found
RIV/00216224:14310/06:00018654
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Oxidation of aromatic and aliphatic hydrocarbons by OH radicals photochemically generated from H2O2 in ice
Original language description
Oxidation of aromatic and saturated aliphatic hydrocarbons (c = 10-3-10-5 mol L-1) by the hydroxyl radicals, photochemically produced from hydrogen peroxide (c = 10-1-10-5 mol L-1), in frozen aqueous solutions was investigated in the temperature range of-20 to -196 C. While aromatic molecules (benzene, phenol, naphthalene, naphthalen-2-ol, or anthracene) underwent primarily addition-elimination reactions to form the corresponding hydroxy compounds, saturated hydrocarbons (cyclohexane, butane, methane)were oxidized to alcohols or carbonyl compounds via hydrogen abstraction and termination reactions. The results suggest that these photoreactions, taking place in a highly concentrated liquid or solidified layers covering the ice crystals, are qualitatively similar to those known to occur in liquid aqueous solutions; however, that probability of any bimolecular reaction in the environment ultimately depends on organic contaminant concentrations and oxidants availability at specific locat
Czech name
Oxidace aromatických a alifatických uhlovodíků OH radikály fotochemicky generovanými v ledu
Czech description
Oxidation of aromatic and saturated aliphatic hydrocarbons (c = 10-3-10-5 mol L-1) by the hydroxyl radicals, photochemically produced from hydrogen peroxide (c = 10-1-10-5 mol L-1), in frozen aqueous solutions was investigated in the temperature range of-20 to -196 C. While aromatic molecules (benzene, phenol, naphthalene, naphthalen-2-ol, or anthracene) underwent primarily addition-elimination reactions to form the corresponding hydroxy compounds, saturated hydrocarbons (cyclohexane, butane, methane)were oxidized to alcohols or carbonyl compounds via hydrogen abstraction and termination reactions. The results suggest that these photoreactions, taking place in a highly concentrated liquid or solidified layers covering the ice crystals, are qualitatively similar to those known to occur in liquid aqueous solutions; however, that probability of any bimolecular reaction in the environment ultimately depends on organic contaminant concentrations and oxidants availability at specific locat
Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
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Result continuities
Project
<a href="/en/project/GA205%2F05%2F0819" target="_blank" >GA205/05/0819: Environmental consequences of photochemical processes in ice and snow</a><br>
Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2006
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Environmental Science & Technology
ISSN
0013-936X
e-ISSN
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Volume of the periodical
40
Issue of the periodical within the volume
24
Country of publishing house
US - UNITED STATES
Number of pages
7
Pages from-to
7668-7674
UT code for WoS article
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EID of the result in the Scopus database
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