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Temperature and pressure dependence study of the reaction of IO radicals with dimethyl sulfide by cavity ring-down laser spectroscopy
被引:39
作者:

Nakano, Y
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机构:
Kyoto Univ, Dept Mol Engn, Kyoto 6068501, Japan Kyoto Univ, Dept Mol Engn, Kyoto 6068501, Japan

Enami, S
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h-index: 0
机构:
Kyoto Univ, Dept Mol Engn, Kyoto 6068501, Japan Kyoto Univ, Dept Mol Engn, Kyoto 6068501, Japan

Nakamichi, S
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机构:
Kyoto Univ, Dept Mol Engn, Kyoto 6068501, Japan Kyoto Univ, Dept Mol Engn, Kyoto 6068501, Japan

Aloisio, S
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机构:
Kyoto Univ, Dept Mol Engn, Kyoto 6068501, Japan Kyoto Univ, Dept Mol Engn, Kyoto 6068501, Japan

Hashimoto, S
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机构:
Kyoto Univ, Dept Mol Engn, Kyoto 6068501, Japan Kyoto Univ, Dept Mol Engn, Kyoto 6068501, Japan

Kawasaki, M
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Kyoto Univ, Dept Mol Engn, Kyoto 6068501, Japan Kyoto Univ, Dept Mol Engn, Kyoto 6068501, Japan
机构:
[1] Kyoto Univ, Dept Mol Engn, Kyoto 6068501, Japan
关键词:
D O I:
10.1021/jp0345147
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 reaction of 10 radicals with dimethyl sulfide was studied using cavity ring-down laser spectroscopy. The reaction rate constant shows both a temperature and pressure dependence. At 100 Torr total pressure, the reaction has reached its high-pressure limit and has a rate constant of (2.5 +/- 0.2) x 10(-13) molecule(-1) cm(3) s(-1) at 298 K. On the basis of the Arrhenius plot in the region of 273-312 K, the reaction has a negative activation energy (E-a = -18.5 +/- 3.8 kJ mol(-1)). The atmospheric implications of these findings are discussed. In light of these new data, DMS oxidation by 10 can compete with oxidation by the hydroxyl radical in the marine boundary layer. Quoted uncertainties are one standard deviation from regression analysis.
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页码:6381 / 6387
页数:7
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