Optimized rate expressions for soot oxidation by OH and O2

被引:50
作者
Guo, Haiqing [1 ]
Anderson, Paul M. [1 ]
Sunderland, Peter B. [1 ]
机构
[1] Univ Maryland, Dept Fire Protect Engn, 3104 JM Patterson Bldg, College Pk, MD 20742 USA
基金
美国国家科学基金会;
关键词
Combustion; Fire; Flames; Particulates; DIESEL-ENGINE SOOT; DIFFUSION FLAMES; LAMINAR METHANE; SURFACE GROWTH; KINETICS; COMBUSTION; COFLOW; MECHANISMS; PRESSURES; PARTICLES;
D O I
10.1016/j.fuel.2016.01.030
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
The two principal soot oxidizers in flames are the hydroxyl radical (OH) and molecular oxygen (O-2). Many soot oxidation rate expressions exist for these oxidizers, but they have considerable disparity and have not been sufficiently validated. To address this, twelve published experimental studies in diffusion flames, premixed flames, thermogravimetric analyzers, and flow reactors are examined. These are all the known studies that measured all of the following quantities at discrete locations: soot oxidation rate, temperature, OH concentration (if nonzero), and O-2 concentration. This yielded 160 measured soot oxidation rates spanning seven orders of magnitude. Optimized soot oxidation rate expressions for OH and O-2 are developed here by maximizing the coefficient of determination between measured and modeled oxidation rates. Oxidation of soot by OH is found to have a negligible activation energy and a collision efficiency of 0.10. The activation energy for O-2 oxidation of soot is 195 kJ/mol, which is higher than previous models. The new expressions for OH and O-2 match the measurements with a regression coefficient of 0.98, compared to 0.79 for the most widely used models. The optimized models indicate that soot oxidation in flames by OH generally dominates over that by O-2. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:248 / 252
页数:5
相关论文
共 42 条
[21]   Numerical modelling of soot formation and oxidation in laminar coflow non-smokifig and smoking ethylene diffusion flames [J].
Liu, F ;
Guo, HS ;
Smallwood, GJ ;
Gülder, ÖL .
COMBUSTION THEORY AND MODELLING, 2003, 7 (02) :301-315
[22]   An assessment of gas-phase reaction mechanisms and soot models for laminar atmospheric-pressure ethylene-air flames [J].
Mehta, R. S. ;
Haworth, D. C. ;
Modest, M. F. .
PROCEEDINGS OF THE COMBUSTION INSTITUTE, 2009, 32 :1327-1334
[23]   PARTIAL EQUILIBRIUM IN THE REACTION ZONE OF METHANE-AIR DIFFUSION FLAMES [J].
MITCHELL, RE ;
SAROFIM, AF ;
CLOMBURG, LA .
COMBUSTION AND FLAME, 1980, 37 (02) :201-206
[24]  
Nagle J., 1962, P 5 C CARB
[25]  
Neoh K.G., 1984, P COMBUST INST, V20, P951
[26]  
NEOH KG, 1980, THESIS MIT CAMBRIDGE
[27]   SHOCK-TUBE MEASUREMENTS OF SOOT OXIDATION RATES [J].
PARK, C ;
APPLETON, JP .
COMBUSTION AND FLAME, 1973, 20 (03) :369-379
[28]   THE OXIDATION OF SOOT AND CARBON-MONOXIDE IN HYDROCARBON DIFFUSION FLAMES [J].
PURI, R ;
SANTORO, RJ ;
SMYTH, KC .
COMBUSTION AND FLAME, 1994, 97 (02) :125-144
[29]   THE OXIDATION OF SOOT AND CARBON-MONOXIDE IN HYDROCARBON DIFFUSION FLAMES, COMBUSTION AND FLAME (VOL 97, PG 125, 1994) [J].
PURI, R ;
SANTORO, RJ ;
SMYTH, KC .
COMBUSTION AND FLAME, 1995, 102 (1-2) :226-228
[30]   Thermal fragmentation and deactivation of combustion-generated soot particles [J].
Raj, Abhijeet ;
Tayouo, Russell ;
Cha, Dongkyu ;
Li, Liang ;
Ismail, Mohamed A. ;
Chung, Suk Ho .
COMBUSTION AND FLAME, 2014, 161 (09) :2446-2457