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
  • [21] Kinetic Study of the OH plus Glyoxal Reaction: Experimental Evidence and Quantification of Direct OH Recycling
    Lockhart, James
    Blitz, Mark
    Heard, Dwayne
    Seakins, Paul
    Shannon, Robin
    JOURNAL OF PHYSICAL CHEMISTRY A, 2013, 117 (43): : 11027 - 11037
  • [22] Kinetic isotope effect in the reaction of oh radical with acetone-D6
    Edit Farkas
    István Szilágyi
    Sándor Dóbé
    Tibor Bérces
    Ferenc Márta
    Reaction Kinetics and Catalysis Letters, 2003, 80 : 351 - 358
  • [23] Kinetic isotope effect in the reaction of OH radical with acetone-d6
    Farkas, E
    Szilágyi, I
    Dóbé, S
    Bérces, T
    Márta, F
    REACTION KINETICS AND CATALYSIS LETTERS, 2003, 80 (02): : 351 - 358
  • [24] Reaction rates and kinetic isotope effects of H2 + OH → H2O + H
    Meisner, Jan
    Kaestner, Johannes
    JOURNAL OF CHEMICAL PHYSICS, 2016, 144 (17):
  • [25] Temperature dependence of stable carbon kinetic isotope effect for the oxidation reaction of ethane by OH radicals: Experimental and theoretical studies
    Piansawan, T.
    Saccon, M.
    Vereecken, L.
    Gensch, I.
    Kiendler-Scharr, A.
    JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2017, 122 (15) : 8310 - 8324
  • [26] Kinetic Isotope Effects in the Study of Organometallic Reaction Mechanisms
    Gomez-Gallego, Mar
    Sierra, Miguel A.
    CHEMICAL REVIEWS, 2011, 111 (08) : 4857 - 4963
  • [27] Chlorine kinetic isotope effects on the haloalkane dehalogenase reaction
    Lewandowicz, A
    Rudzinski, J
    Tronstad, L
    Widersten, M
    Ryberg, P
    Matsson, O
    Paneth, P
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (19) : 4550 - 4555
  • [28] Nitrogen and deuterium kinetic isotope effects on the Menshutkin reaction
    SzylhabelGodala, A
    Madhavan, S
    Rudzinski, J
    OLeary, MH
    Paneth, P
    JOURNAL OF PHYSICAL ORGANIC CHEMISTRY, 1996, 9 (01) : 35 - 40
  • [29] EVALUATION OF KINETIC ISOTOPE-EFFECTS ON REACTION RADICALS
    GALIMOV, EM
    ZHURNAL FIZICHESKOI KHIMII, 1972, 46 (11): : 2899 - 2901
  • [30] A shock tube kinetic study on the branching ratio of methanol plus OH reaction
    Liu, Dapeng
    Giri, Binod Raj
    Farooq, Aamir
    PROCEEDINGS OF THE COMBUSTION INSTITUTE, 2019, 37 (01) : 153 - 162