Ephemeral collision complexes mediate chemically termolecular transformations that affect system chemistry

被引:112
作者
Burke, Michael P. [1 ]
Klippenstein, Stephen J. [2 ]
机构
[1] Columbia Univ, Data Sci Inst, Dept Chem Engn, Dept Mech Engn, New York, NY 10027 USA
[2] Argonne Natl Lab, Chem Sci & Engn Div, Argonne, IL 60439 USA
关键词
MASTER EQUATION; TEMPERATURE; HYDROGEN; DEPENDENCE; KINETICS; RATES; ATOM;
D O I
10.1038/nchem.2842
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Termolecular association reactions involve ephemeral collision complexes-formed from the collision of two molecules that collide with a third and chemically inert 'bath gas' molecule that simply transfers energy to/from the complex. These collision complexes are generally not thought to react chemically on collision with a third molecule in the gas-phase systems of combustion and planetary atmospheres. Such 'chemically termolecular' reactions, in which all three molecules are involved in bond making and/or breaking, were hypothesized long ago in studies establishing radical chain branching mechanisms, but were later concluded to be unimportant. Here, with data from ab initio master equation and kinetic-transport simulations, we reveal that reactions of H + O-2 collision complexes with other radicals constitute major kinetic pathways under common combustion situations. These reactions are also found to influence flame propagation speeds, a common measure of global reactivity. Analogous chemically termolecular reactions mediated by ephemeral collision complexes are probably of significance in various combustion and planetary environments.
引用
收藏
页码:1078 / 1082
页数:5
相关论文
共 39 条
[1]   THE 1ST LIMIT OF THE HYDROGEN+OXYGEN REACTION IN POTASSIUM CHLORIDE-COATED VESSELS [J].
BALDWIN, RR .
TRANSACTIONS OF THE FARADAY SOCIETY, 1956, 52 (10) :1344-1354
[2]   Master equation analysis of pressure-dependent atmospheric reactions [J].
Barker, JR ;
Golden, DM .
CHEMICAL REVIEWS, 2003, 103 (12) :4577-4591
[3]   SHOCK SYNTHESIS OF AMINO ACIDS IN SIMULATED PRIMITIVE ENVIRONMENTS [J].
BARNUN, A ;
BARNUN, N ;
BAUER, SH ;
SAGAN, C .
SCIENCE, 1970, 168 (3930) :470-&
[4]   ON THE INTERPRETATION OF HALOGEN ATOM RECOMBINATION RATES [J].
BUNKER, DL ;
DAVIDSON, N .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1958, 80 (19) :5090-5096
[5]   Towards a quantitative understanding of the role of non-Boltzmann reactant distributions in low temperature oxidation [J].
Burke, Michael P. ;
Goldsmith, C. Franklin ;
Georgievskii, Yuri ;
Klippenstein, Stephen J. .
PROCEEDINGS OF THE COMBUSTION INSTITUTE, 2015, 35 :205-213
[6]   A quantitative explanation for the apparent anomalous temperature dependence of OH + HO2 = H2O + O2 through multi-scale modeling [J].
Burke, Michael P. ;
Klippenstein, Stephen J. ;
Harding, Lawrence B. .
PROCEEDINGS OF THE COMBUSTION INSTITUTE, 2013, 34 :547-555
[7]   Comprehensive H2/O2 kinetic model for high-pressure combustion [J].
Burke, Michael P. ;
Chaos, Marcos ;
Ju, Yiguang ;
Dryer, Frederick L. ;
Klippenstein, Stephen J. .
INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, 2012, 44 (07) :444-474
[8]   Dynamics of the Reaction of Methane with Chlorine Atom on an Accurate Potential Energy Surface [J].
Czako, Gabor ;
Bowman, Joel M. .
SCIENCE, 2011, 334 (6054) :343-346
[9]  
Dixon-Lewis G., 1977, Comprehensive Chemical Kinetics, P1