Improved Shock Tube Measurement of the CH4 + Ar = CH3 + H + Ar Rate Constant using UV Cavity-Enhanced Absorption Spectroscopy of CH3

被引:29
作者
Wang, Shengkai [1 ]
Davidson, David F. [1 ]
Hanson, Ronald K. [1 ]
机构
[1] Stanford Univ, Mech Engn, High Temp Gasdynam Lab, Stanford, CA 94305 USA
关键词
ENHANCED ABSORPTION-SPECTROSCOPY; RATE CONSTANTS; THERMAL-DECOMPOSITION; PRESSURE-DEPENDENCE; METHANE; DISSOCIATION; LASER; KINETICS; OXIDATION;
D O I
10.1021/acs.jpca.6b02572
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
We report an improved measurement for the rate constant of methane dissociation in argon (CH4 + Ar = CH3 + H + Ar) behind reflected shock waves. The experiment was conducted using a sub-parts per million sensitivity CH3 diagnostic recently developed in our laboratory based on ultraviolet cavity-enhanced absorption spectroscopy. The high sensitivity of this diagnostic allowed for measurements of quantitatively resolved CH3 time histories during the initial stage of CH4 pyrolysis, where the reaction system is clean and free from influences of secondary reactions and temperature change. This high sensitivity also allowed extension of our measurement range to much lower temperatures (<1500 K). The current-reflected shock measurements were performed at temperatures between 1487 and 1866 K and pressures near 1.7 atm, resulting in the following Arrhenius rate constant expression for the title reaction: k(1.7 atm) = 3.7 x 10(16) exp(-42 200 KIT) cm(3)/mol.s, with a 2 sigma uncertainty factor of 1.25. The current data are in good consensus with various theoretical and review studies, but at the low temperature end they suggest a slightly higher (up to 35%) rate constant compared to these previous results. A re-evaluation of previous and current experimental data in the falloff region was also performed, yielding updated expressions for both the low-pressure limit and the high-pressure limit rate constants and improved agreement with all existing data.
引用
收藏
页码:5427 / 5434
页数:8
相关论文
共 38 条
[1]  
[Anonymous], 36 INT S COMB UNPUB
[2]  
[Anonymous], 2015, Active Thermochemical Tables (ATcT) values based on ver. 1.118 of the Thermochemical Network
[3]   PRESSURE-DEPENDENCE OF METHANE DISSOCIATION [J].
BARNES, RW ;
PRATT, GL ;
WOOD, SW .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS II, 1989, 85 :229-238
[4]   Evaluated kinetic data for combustion modeling: Supplement II [J].
Baulch, DL ;
Bowman, CT ;
Cobos, CJ ;
Cox, RA ;
Just, T ;
Kerr, JA ;
Pilling, MJ ;
Stocker, D ;
Troe, J ;
Tsang, W ;
Walker, RW ;
Warnatz, J .
JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA, 2005, 34 (03) :757-1397
[5]  
Bowman CT., 1975, Symp Int Combust, V15, P869, DOI DOI 10.1016/S0082-0784(75)80354-7
[6]   EXPERIMENTAL AND RRKM MODELING STUDY OF THE CH3+H AND CH3+D REACTIONS [J].
BROUARD, M ;
MACPHERSON, MT ;
PILLING, MJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1989, 93 (10) :4047-4059
[7]   THERMAL-DECOMPOSITION OF METHANE .1. KINETICS OF PRIMARY DECOMPOSITION TO C2H6 + H2 - RATE CONSTANT FOR HOMOGENEOUS UNIMOLECULAR DISSOCIATION OF METHANE AND ITS PRESSURE-DEPENDENCE [J].
CHEN, CJ ;
BACK, MH ;
BACK, RA .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1975, 53 (23) :3580-3590
[8]   PRESSURE-DEPENDENCE OF RATE CONSTANT OF REACTION H + CH3-]CH4 [J].
CHENG, JT ;
YEH, CT .
JOURNAL OF PHYSICAL CHEMISTRY, 1977, 81 (21) :1982-1984
[9]  
Davidson D., 1992, Sympos. (Int.) Combust., V24, P589
[10]   COMMUNICATION - REVISED VALUES FOR THE RATE COEFFICIENTS OF ETHANE AND METHANE DECOMPOSITION [J].
DAVIDSON, DF ;
HANSON, RK ;
BOWMAN, CT .
INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, 1995, 27 (03) :305-308