Predictions of the sulfur and carbon kinetic isotope effects in the OH plus OCS reaction

被引:13
|
作者
Schmidt, J. A. [1 ]
Johnson, M. S. [1 ]
Jung, Y. [2 ]
Danielache, S. O. [3 ]
Hattori, S. [4 ]
Yoshida, N. [4 ]
机构
[1] Univ Copenhagen, Dept Chem, DK-2100 Copenhagen O, Denmark
[2] Korea Adv Inst Sci & Technol, Grad Sch EEWS, Taejon 305701, South Korea
[3] Tokyo Inst Technol, Dept Earth & Planetary Sci, Meguro Ku, Tokyo 1528551, Japan
[4] Tokyo Inst Technol, Dept Environm Chem & Engn, Yokohama, Kanagawa 2268502, Japan
关键词
CORRELATED MOLECULAR CALCULATIONS; GAUSSIAN-BASIS SETS; TRIPLE EXCITATIONS; RATE CONSTANTS; AB-INITIO; SULFIDE; FRACTIONATION; STRATOSPHERE; SPECTROSCOPY; RADICALS;
D O I
10.1016/j.cplett.2012.02.049
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 S-34 and C-13 isotopic fractionations in the OCS + OH reaction are investigated using RRKM-theory. The reaction proceeds via different channels, at low pressures a channel leading to CO + SOH dominates. While with increasing pressure an adduct forming channel becomes competitive. The resulting overall rate constant is not strongly dependent on pressure and agrees well with experiments. The competition between channels makes the fractionation constants highly pressure dependent, however the sulfur-34 fractionation constant varies only from about -5 parts per thousand to 0 parts per thousand in the troposphere and lower stratosphere. The carbon-13 isotopic fractionation is stronger; between -40 parts per thousand and -70 parts per thousand in the troposphere and lower stratosphere. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:64 / 69
页数:6
相关论文
共 50 条
  • [11] On adduct formation and reactivity in the OCS plus OH reaction: A combined theoretical and experimental study
    Schmidt, Johan A.
    Kyte, Mildrid
    Osterstrom, Freja F.
    Joelsson, Lars M. T.
    Knap, Hasse C.
    Jorgensen, Solvejg
    Nielsen, Ole John
    Murakami, Tatsuhiro
    Johnson, Matthew S.
    CHEMICAL PHYSICS LETTERS, 2017, 675 : 111 - 117
  • [12] Quantum dynamics calculations reveal temperature independence of kinetic isotope effect of the OH plus HBr/DBr reaction
    Wang, Yuping
    Wang, Dunyou
    JOURNAL OF CHEMICAL PHYSICS, 2018, 149 (03):
  • [13] DEUTERIUM AND C-13 KINETIC ISOTOPE EFFECTS FOR THE REACTION OF OH WITH CH4
    MELISSAS, VS
    TRUHLAR, DG
    JOURNAL OF CHEMICAL PHYSICS, 1993, 99 (05): : 3542 - 3552
  • [14] Carbon kinetic isotope effects for the reactions of atmospheric NMHC with OH, Cl and O3.
    Anderson, RS
    Iannone, R
    Rudolph, J
    Thompson, AE
    Huang, L
    Ernst, D
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2002, 224 : U326 - U326
  • [15] Deconstructing experimental rate constant measurements: Obtaining intrinsic reaction parameters, kinetic isotope effects, and tunneling coefficients from kinetic data for OH plus methane, ethane and cyclohexane
    Sage, AM
    Donahue, NM
    JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2005, 176 (1-3) : 238 - 249
  • [16] KINETIC ISOTOPE EFFECTS AND ORGANIC REACTION MECHANISMS
    GOLDSTEIN, MJ
    SCIENCE, 1966, 154 (3757) : 1616 - +
  • [17] KINETIC ISOTOPE EFFECTS IN HYDROGEN ELECTRODE REACTION
    MCINTYRE, JD
    SALOMON, M
    JOURNAL OF PHYSICAL CHEMISTRY, 1968, 72 (07): : 2431 - &
  • [18] Temperature-dependent kinetic isotope effects in the gas-phase reaction: OH+HBr
    Jaramillo, VI
    Smith, MA
    JOURNAL OF PHYSICAL CHEMISTRY A, 2001, 105 (24): : 5854 - 5859
  • [19] Kinetic Isotope Effects on Dehalogenations at an Aromatic Carbon
    Dybala-Defratyka, Agnieszka
    Szatkowski, Lukasz
    Kaminski, Rafal
    Wujec, Monika
    Siwek, Agata
    Paneth, Piotr
    ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2008, 42 (21) : 7744 - 7750
  • [20] KINETIC SULFUR ISOTOPE EFFECTS IN THE THERMAL-DECOMPOSITION OF PYRITE
    KAJIWARA, Y
    SASAKI, A
    MATSUBAYA, O
    GEOCHEMICAL JOURNAL, 1981, 15 (04) : 193 - 197