Kinetics of ethane oxidation
โ Scribed by Philippe Dagaut; Michel Cathonnet; Jean-claude Boettner
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 922 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0538-8066
No coin nor oath required. For personal study only.
โฆ Synopsis
Ethane oxidation in jet-stirred reactor has recently been investigated at high temperature (800-1200 K) in the pressure range 1-10 atm and molecular species (HZ, CO, Con, CH,, G H z , CzH4, C2H6) concentration profiles were obtained by probe sampling and GC analysis. Ethane oxidation was modeled using a comprehensive kinetic reaction mechanism including the most recent findings concerning the kinetics of the reactions involved in the oxidation of CI -C, hydrocarbons. The proposed mechanism is able to reproduce experimental data obtained in our high-pressure jet stirred reactor and ignition delay times measured in shock tube in the pressure range 1-13 atm, for temperatures extending from 800 to 2000 K and equivalence ratios of 0.1 to 2. It is also able to reproduce atoms concentrations (H,O) measured in shock tube at =2 atm. The same detailed kinetic mechanism can also be used to model the oxidation of methane, ethylene, propyne, and allene in similar conditions.
๐ SIMILAR VOLUMES
Chemically activated ethane, with an excitation energy of 114.9 f 2 kcal/mole, was forme; by reaction with methane of excited singlet methylene radicals produced by the 4358 A photolysis of diazomethane. A decomposition rate constant of (4.6 =k 1.2) X l o 9 sec-' was measured for the chemically acti
The kinetics of ethane hydrate formation after commencement of nucleation were studied at temperatures from 274 to 282 K over a pressure range of 0.6-2.6 MPa. Gaseous ethane was reacted with liquid water in a semi-batch stirred tank reactor. The results of the experiments revealed that the reaction
The kinetics of ethane oxidation was studied a t 320,340,353 and 38OoC, mixture composition 2 C ~H G + 1 02. and total pressure 609 torr. I t was found that a t 320ยฐC CH20 and CH3CHO were branching agents. A series of experiments was conducted on 2C2Hfi + 0 2 oxidation in the presence of 0.7% 14C-la