標題: Ab Initio Chemical Kinetics for the NH2 + HNOx Reactions, Part I: Kinetics and Mechanism for NH2 + HNO
作者: Xu, Shucheng
Lin, M. C.
應用化學系
Department of Applied Chemistry
公開日期: 1-Nov-2009
摘要: The kinetics and mechanism for the reaction of NH2 with HNO have been investigated by ab initio calculations with rate constant prediction. The potential energy surface of this reaction has been computed by single-point calculations at the CCSD(T)/6-311+G(3df, 2p) level based on geometries optimized at the CCSD/6-311++G(d, p) level. The major products of this reaction were found to be NH3 + NO formed by H-abstraction via a long-lived H2N center dot center dot center dot HNO complex and the H2NN(H)O radical intermediate formed by association with 26.9 kcal/mol binding energy. The rate constants for formation of primary products in the temperature range of 300-3000 K were predicted by variational transition state or RRKM theories. The predicted total rate constants at the 760 Torr At pressure can be represented by k(total) = 3.83 x 10(-20) x T(+2.47)exp(1450/T) at T = 300-600 K; 2.58 x 10(-22) x T+3.15 exp(1831/T) cm(3) molecule(-1) s(-1) at T = 600-3000 K. The branching ratios of major channels at 760 Torr Ar pressure are predicted: k(1) + k(3) + k(4) producing NH3 + NO accounts for 0.59-0.90 at T = 300-3000 K peaking around 1000 K, k(2) accounts for 0.41-0.03 at T = 300-600 K decreasing with temperature, and k(5) accounts for 0.07-0.27 at T > 600 K increasing gradually with temperature. The NH3 + NO formation rate constant was found to be a factor of 3-10 smaller than that of the isoelectronic reaction CH3 + HNO producing CH4 + NO, which has been shown to take place by barrierless H-abstraction without involving a hydrogen-bonding complex as in the NH2 case. (C) 2009 Wiley Periodicals, Inc. Int J Chem Kinet 41: 667-677, 2009
URI: http://dx.doi.org/10.1002/kin.20453
http://hdl.handle.net/11536/149836
ISSN: 0538-8066
DOI: 10.1002/kin.20453
期刊: INTERNATIONAL JOURNAL OF CHEMICAL KINETICS
Volume: 41
起始頁: 667
結束頁: 677
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