INVESTIGATION OF THE (CH2)-C-3+O-2 REACTION IN SHOCK-WAVES

被引:52
作者
DOMBROWSKY, C
WAGNER, HG
机构
来源
BERICHTE DER BUNSEN-GESELLSCHAFT-PHYSICAL CHEMISTRY CHEMICAL PHYSICS | 1992年 / 96卷 / 08期
关键词
CHEMICAL KINETICS; ENERGY TRANSFER; RADICALS; SHOCK WAVES; SPECTROSCOPY;
D O I
10.1002/bbpc.19920960815
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
The reaction of (CH2)-C-3 with O2 was investigated in incident shock waves for pressures near 1 bar and temperatures from 1000 to about 1800 K. (CH2)-C-3 source was diazomethane. The concentration time curves of CO and CO2 were obtained from infrared emission, the OH profiles by laser absorption measurements. Data for O and H atom formation in this reaction were reported recently. - The measurements show that about a quarter of the reaction proceeds by forming radicals directly. Three quarters of the reaction form stable products only. Main reaction product is CO with a CO to CO2 ratio near 4:1. Direct formation of OH does not exceed a few percent. A reaction channel distribution is given. - Rate constants for the total reaction (CH2)-C-3 + O2 obtained by computer simulation of the product profiles in the temperature range mentioned are below the data extrapolated from measurements performed by Vinckier et al. and Bley et al. in the temperature range around room temperature. A rate expression fitting the measured date over the whole temperature range is reported.
引用
收藏
页码:1048 / 1055
页数:8
相关论文
共 34 条
[21]   IN DEFENSE OF OBJECTIVIST ART CRITICISM [J].
LICHTENBERT, RH .
JOURNAL OF AESTHETIC EDUCATION, 1984, 18 (04) :108-113
[22]   MASS-SPECTROMETRIC DETECTION OF DIOXIRANE, H2COO, AND ITS DECOMPOSITION PRODUCTS, H-2 AND CO, FROM REACTION OF OZONE WITH ETHYLENE [J].
MARTINEZ, RI ;
HUIE, RE ;
HERRON, JT .
CHEMICAL PHYSICS LETTERS, 1977, 51 (03) :457-459
[23]   SYSTEMATICS OF VIBRATIONAL RELAXATION [J].
MILLIKAN, RC ;
WHITE, DR .
JOURNAL OF CHEMICAL PHYSICS, 1963, 39 (12) :3209-&
[24]   MASS SPECTRA AND APPEARANCE POTENTIALS OF DIAZIRINE AND DIAZOMETHANE [J].
PAULETT, GS ;
ETTINGER, R .
JOURNAL OF CHEMICAL PHYSICS, 1963, 39 (03) :825-&
[25]  
PAULETT GS, 1963, J CHEM PHYS, V39, P3524
[26]   FLASH-PHOTOLYSIS OF KETENE - PHOTOLYSIS MECHANISM AND RATE CONSTANTS FOR SINGLET AND TRIPLET METHYLENE [J].
PILLING, MJ ;
ROBERTSON, JA .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1977, 73 :968-984
[27]   VIBRATIONAL-RELAXATION OF OH (CHI-2-PI-I, V=2) [J].
RENSBERGER, KJ ;
JEFFRIES, JB ;
CROSLEY, DR .
JOURNAL OF CHEMICAL PHYSICS, 1989, 90 (04) :2174-2181
[28]   TRACER STUDIES OF REACTIONS OF SINGLET AND TRIPLET METHYLENE IN GAS-PHASE [J].
ROWLAND, FS ;
LEE, PST ;
MONTAGUE, DC ;
RUSSELL, RL .
FARADAY DISCUSSIONS, 1972, 53 :111-118
[29]   THERMAL UNIMOLECULAR DECOMPOSITION OF FORMIC-ACID [J].
SAITO, K ;
KAKUMOTO, T ;
KURODA, H ;
TORII, S ;
IMAMURA, A .
JOURNAL OF CHEMICAL PHYSICS, 1984, 80 (10) :4989-4996
[30]   COLLISION DYNAMICS OF OH(X2-PI-I,V=12) [J].
SAPPEY, AD ;
COPELAND, RA .
JOURNAL OF CHEMICAL PHYSICS, 1990, 93 (08) :5741-5746