Atmospheric chemistry of C3-C6 cycloalkanecarbaldehydes

被引:23
作者
D'Anna, B
Wisthaler, A
Andreasen, O
Hansel, A
Hjorth, J
Jensen, NR
Nielsen, CJ
Stenstrom, Y
Viidanoja, J
机构
[1] Univ Oslo, Dept Chem, N-0315 Oslo, Norway
[2] Univ Innsbruck, Inst Ionenphys, A-6020 Innsbruck, Austria
[3] European Commiss, DJ Joint Res Ctr, Inst Environm & Sustainabil, Climate Change Unit, I-21020 Ispra, Italy
[4] Agr Univ Norway, Chem Sect, Dept Chem Biotechnol & Food Sci, N-1432 As, Norway
关键词
D O I
10.1021/jp044495g
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The rate coefficients for the gas phase reaction of NO3 and OH radicals with a series of cycloalkanecarbaldehydes have been measured in purified air at 298 +/- 2 K and 760 +/- 10 Torr by the relative rate method using a static reactor equipped with long-path Fourier transform infrared (FT-IR) detection. The values obtained for the OH radical reactions (in units of 10(-11) cm(3) molecule(-1) s(-1)) were the following: cyclopropanecarbaldehyde, 2.13 +/- 0.05; cyclobutanecarbaldehyde, 2.66 +/- 0.06; cyclopentanecarbaldehyde, 3.27 +/- 0.07; cyclohexanecarbaldehyde, 3.75 +/- 0.05. The values obtained for the NO3 radical reactions (in units of 10(-14) cm(3) molecule(-1) s(-1)) were the following: cyclopropanecarbaldehyde, 0.61 +/- 0.04; cyclobutanecarbaldehyde, 1.99 +/- 0.06; cyclopentanecarbaldehyde, 2.55 +/- 0.10; cyclohexanecarbaldehyde, 3.19 +/- 0.12. Furthermore, the reaction products with OH radicals have been investigated using long-path FT-IR spectroscopy and proton-transfer-reaction mass spectrometry (PTR-MS). The measured carbon balances were in the range 89-97%, and the identified products cover a wide spectrum of compounds including nitroperoxycarbonyl cycloalkanes, cycloketones, cycloalkyl nitrates, multifunctional compounds containing carbonyl, hydroxy, and nitrooxy functional groups, HCOOH, HCHO, CO, and CO2.
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页码:5104 / 5118
页数:15
相关论文
共 78 条
[41]   Newly characterized products and composition of secondary aerosols from the reaction of α-pinene with ozone [J].
Jang, M ;
Kamens, RM .
ATMOSPHERIC ENVIRONMENT, 1999, 33 (03) :459-474
[42]  
JENSEN NRV, 2003, CONTR 1 INT C PROT T
[43]   Isomerization of simple alkoxyl radicals: New temperature-dependent rate data and structure activity relationship [J].
Johnson, D ;
Cassanelli, P ;
Cox, RA .
JOURNAL OF PHYSICAL CHEMISTRY A, 2004, 108 (04) :519-523
[44]  
Johnson M. R., 1971, ORG SYNTH, V51, P11
[45]   Atmospheric oxidation mechanism of n-butane: The fate of alkoxy radicals [J].
Jungkamp, TPW ;
Smith, JN ;
Seinfeld, JH .
JOURNAL OF PHYSICAL CHEMISTRY A, 1997, 101 (24) :4392-4401
[46]   PREPARATION OF ORGANIC NITRATES FROM ALCOHOLS AND N2O5 FOR SPECIES IDENTIFICATION IN ATMOSPHERIC SAMPLES [J].
KAMES, J ;
SCHURATH, U ;
FLOCKE, F ;
VOLZTHOMAS, A .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 1993, 16 (04) :349-359
[47]   OBSERVATION OF HYDROXYCARBONYLS FROM THE OH RADICAL-INITIATED REACTION OF ISOPRENE [J].
KWOK, ESC ;
ATKINSON, R ;
AREY, J .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1995, 29 (09) :2467-2469
[48]   ESTIMATION OF HYDROXYL RADICAL REACTION-RATE CONSTANTS FOR GAS-PHASE ORGANIC-COMPOUNDS USING A STRUCTURE-REACTIVITY RELATIONSHIP - AN UPDATE [J].
KWOK, ESC ;
ATKINSON, R .
ATMOSPHERIC ENVIRONMENT, 1995, 29 (14) :1685-1695
[49]   Gas-phase OH oxidation of monoterpenes: Gaseous and particulate products [J].
Larsen, BR ;
Di Bella, D ;
Glasius, M ;
Winterhalter, R ;
Jensen, NR ;
Hjorth, J .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 2001, 38 (03) :231-276
[50]   Proton-transfer-reaction mass spectrometry (PTR-MS): on-line monitoring of volatile organic compounds at pptv levels [J].
Lindinger, W ;
Hansel, A ;
Jordan, A .
CHEMICAL SOCIETY REVIEWS, 1998, 27 (05) :347-354