Rate constants for the gas-phase reactions of the hydroxyl radical with isoprene, α- and β-pinene, and limonene as a function of temperature

被引:75
作者
Gill, KJ
Hites, RA [1 ]
机构
[1] Indiana Univ, Sch Publ & Environm Affairs, Environm Sci Res Ctr, Bloomington, IN 47405 USA
[2] Indiana Univ, Dept Chem, Bloomington, IN 47405 USA
关键词
D O I
10.1021/jp013532q
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
Rate constants for the gas-phase reactions of the hydroxyl radical with the biogenic hydrocarbons isoprene, alpha- and beta-pinene, and limonene were measured using the relative rate technique over the temperature range 295-364 K and at 760 Torr total pressure. OH was produced by the photolysis of H2O2, and helium was the diluent gas. The reactants were detected by on-line mass spectrometry, which resulted in high time resolution allowing for large amounts of data to be collected and used in the determination of the Arrhenius parameters. Many experiments were performed over the temperature range of interest leading to more accurate parameters than previous investigations, which have relied on rate constants measured at three or fewer temperatures. The following Arrhenius expressions have been determined for these reactions (in units of cm(3) molecule(-1) s(-1)): isoprene, 2.56(-0.31)(+0.35) x 10(-11) exp[(408 +/- 42)/T]; alpha-pinene, 1.17(-0.18)(+0.21) x 10(-11) exp[(436 +/- 53)/T]; beta-pinene, 1.47(-0.21)(+0.24) x 10(-11) exp[(467 +/- 50)/T]; limonene, 4.20(-0.51)(+0.59) x 10(-11) exp[(401 +/- 43)/T]. The Arrhenius parameters determined here for the reaction of OH with beta-pinene are significantly different than the current recommendation, and the parameters given here for limonene are the first to be reported.
引用
收藏
页码:2538 / 2544
页数:7
相关论文
共 30 条
[1]   System to measure relative rate constants of semivolatile organic compounds with hydroxyl radicals [J].
Anderson, PN ;
Hites, RA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1996, 30 (01) :301-306
[2]   OH radical reactions: The major removal pathway for polychlorinated biphenyls from the atmosphere [J].
Anderson, PN ;
Hites, RA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1996, 30 (05) :1756-1763
[3]   PRODUCT STUDY OF THE GAS-PHASE REACTIONS OF MONOTERPENES WITH THE OH RADICAL IN THE PRESENCE OF NOX [J].
AREY, J ;
ATKINSON, R ;
ASCHMANN, SM .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1990, 95 (D11) :18539-18546
[4]   Products of the gas phase reactions of the OH radical with α- and β-pinene in the presence of NO [J].
Aschmann, SM ;
Reissell, A ;
Atkinson, R ;
Arey, J .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1998, 103 (D19) :25553-25561
[5]   RATE CONSTANTS FOR THE GAS-PHASE REACTIONS OF THE OH-RADICAL WITH A SERIES OF MONOTERPENES AT 294 +/- 1-K [J].
ATKINSON, R ;
ASCHMANN, SM ;
PITTS, JN .
INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, 1986, 18 (03) :287-299
[6]   RATE CONSTANTS FOR THE REACTION OF OH RADICALS WITH A SERIES OF ALKENES AND DIALKENES AT 295 +/- 1-K [J].
ATKINSON, R ;
ASCHMANN, SM .
INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, 1984, 16 (10) :1175-1186
[7]   Gas-phase tropospheric chemistry of volatile organic compounds .1. Alkanes and alkenes [J].
Atkinson, R .
JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA, 1997, 26 (02) :215-290
[8]   RATE CONSTANTS FOR THE REACTION OF OH RADICALS WITH A SERIES OF ALKANES AND ALKENES AT 299 +/- 2-K [J].
ATKINSON, R ;
ASCHMANN, SM ;
WINER, AM ;
PITTS, JN .
INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, 1982, 14 (05) :507-516
[9]   Reaction of OH with dimethyl sulfide (DMS) .1. Equilibrium constant for OH+DMS reaction and the kinetics of the OH center dot DMS+O-2 reaction [J].
Barone, SB ;
Turnipseed, AA ;
Ravishankara, AR .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (35) :14694-14702
[10]   Polychlorinated dibenzo-p-dioxins and dibenzofurans: Gas phase hydroxyl radical reactions and related atmospheric removal [J].
Brubaker, WW ;
Hites, RA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1997, 31 (06) :1805-1810