When Rate Constants Are Not Enough

被引:19
作者
Barker, John R. [1 ]
Frenklach, Michael [2 ]
Golden, David M. [3 ]
机构
[1] Univ Michigan, Dept Atmospher Ocean & Space Sci, Ann Arbor, MI 48109 USA
[2] Univ Calif Berkeley, Dept Mech Engn, Berkeley, CA 94720 USA
[3] Stanford Univ, Dept Mech Engn, Stanford, CA 94305 USA
基金
美国国家科学基金会;
关键词
MASTER EQUATION ANALYSIS; CHANNEL UNIMOLECULAR REACTIONS; INTERMOLECULAR ENERGY-TRANSFER; THERMAL-ACTIVATION REACTIONS; MULTIPLE-WELL; RATE COEFFICIENTS; ISOMERIZATION-REACTIONS; STOCHASTIC SIMULATION; CHEMICAL-REACTION; BRANCHING RATIOS;
D O I
10.1021/acs.jpca.5b00640
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
Real-world chemical systems consisting of multiple isomers and multiple reaction channels often react significantly prior to attaining a steady state energy distribution (SED). Detailed elementary reaction models, which implicitly require SED conditions, may be invalid when non-steady-state energy distributions (NSED) exist. NSED conditions may result in reaction rates and product yields that are different from those expected for SED conditions, although this problem is to some extent reduced by using phenomenological models and rate constants. The present study defines pragmatic diagnostics useful for identifying NSED conditions in stochastic master equation simulations. A representative example is presented for each of four classes of common combustion species: RO2, radicals, aliphatic hydrocarbons, alkyl radicals, and polyaromatic radicals. An example selected from the seminal work of Tsang et al. demonstrates that stochastic simulations and eigenvalue methods for solving the master equation predict the same NSED effects. NSED effects are common under relatively moderate combustion conditions, and accurate simulations may require a master equation analysis.
引用
收藏
页码:7451 / 7461
页数:11
相关论文
共 51 条
[41]   COLLISIONAL ENERGY TRANSFER . THERMAL UNIMOLECULAR SYSTEMS IN LOW-PRESSURE REGION [J].
TARDY, DC ;
RABINOVITCH, BS .
JOURNAL OF CHEMICAL PHYSICS, 1966, 45 (10) :3720-+
[42]   Master equation analysis of thermal activation reactions: Energy-transfer constraints on falloff behavior in the decomposition of reactive intermediates with low thresholds [J].
Tsang, W ;
Bedanov, V ;
Zachariah, MR .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (10) :4011-4018
[43]   Master equation analysis of intermolecular energy transfer in multiple-well, multiple-channel unimolecular reactions.: II.: Numerical methods and application to the mechanism of the C2H5+O2 reaction [J].
Venkatesh, PK ;
Dean, AM ;
Cohen, MH ;
Carr, RW .
JOURNAL OF CHEMICAL PHYSICS, 1999, 111 (18) :8313-8329
[44]   Master equation analysis of intermolecular energy transfer in multiple-well, multiple-channel unimolecular reactions .1. Basic theory [J].
Venkatesh, PK ;
Dean, AM ;
Cohen, MH ;
Carr, RW .
JOURNAL OF CHEMICAL PHYSICS, 1997, 107 (21) :8904-8916
[45]   Stochastic simulation of chemically activated unimolecular reactions [J].
Vereecken, L ;
Huyberechts, G ;
Peeters, J .
JOURNAL OF CHEMICAL PHYSICS, 1997, 106 (16) :6564-6573
[46]   Ab initio barrier heights and branching ratios of isomerization reactions of a branched alkyl radical [J].
Viskolcz, B ;
Lendvay, G ;
Seres, L .
JOURNAL OF PHYSICAL CHEMISTRY A, 1997, 101 (38) :7119-7127
[47]   On modeling the pressure-dependent photoisomerization of trans-stilbene by including slow intramolecular vibrational energy redistribution [J].
Weston, Ralph E., Jr. ;
Barker, John R. .
JOURNAL OF PHYSICAL CHEMISTRY A, 2006, 110 (25) :7888-7897
[48]   HO+CO Reaction Rates and H/D Kinetic Isotope Effects: Master Equation Models with ab Initio SCTST Rate Constants [J].
Weston, Ralph E., Jr. ;
Thanh Lam Nguyen ;
Stanton, John F. ;
Barker, John R. .
JOURNAL OF PHYSICAL CHEMISTRY A, 2013, 117 (05) :821-835
[49]   COLLISION THEORY OF CHEMICAL REACTION RATES [J].
WIDOM, B .
ADVANCES IN CHEMICAL PHYSICS, 1963, 5 :353-386