𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Ignition and oxidation of 1-hexene/toluene mixtures in a shock tube and a jet-stirred reactor: Experimental and kinetic modeling study

✍ Scribed by M. Yahyaoui; N. Djebaïli-Chaumeix; P. Dagaut; C.-E. Paillard; B. Heyberger; G. Pengloan


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
887 KB
Volume
39
Category
Article
ISSN
0538-8066

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

The oxidation of several binary mixtures 1‐hexene/toluene has been investigated both in a shock tube and in a jet‐stirred reactor (JSR). The self‐ignition behavior of binary mixtures was compared to that of neat hydrocarbons studied under the same conditions. Furthermore, molecular species concentration profiles were measured by probe‐sampling and GC/MS, FID, TCD analyses for the oxidation of the mixtures in a JSR. Experiments were carried out over the temperature range 750–1860 K. Mixtures were examined under two pressures 0.2 and 1 MPa, with 0.1% initial concentration of fuel. The equivalence ratio was varied from 0.5 to 1.5. The experiments were modeled using a detailed chemical kinetic reaction mechanism. The modeling study showed that interactions between hydrocarbons submechanisms were not limited to small reactive radicals. Other types of interactions involving hydrocarbon fragments derived from the oxidation of the fuel components must be considered. These interactions mainly consist of hydrogen abstraction reactions. For example, benzyl radical that is the major radical produced from the oxidation of toluene at high temperature can abstract hydrogen from 1‐hexene and their products such as hexenyl radicals. Similarly, propyl, allyl, and hexenyl radicals that are the major radicals produced during 1‐hexene oxidation at high temperature can abstract hydrogen from toluene. Improved modeling was achieved when such interaction reactions were included in the model. Good agreement between experimental and calculated data was obtained using the proposed detailed chemical kinetic scheme. © 2007 Wiley Periodicals, Inc. Int J Chem Kinet 39: 518–538, 2007


📜 SIMILAR VOLUMES


The oxidation of ethylene oxide in a jet
✍ Philippe Dagaut; David Voisin; Michel Cathonnet; Marguerite Mcguinness; John M. 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 503 KB

The oxidation of ethylene oxide (C2H40) has been investigated in a jet-stirred reactor at high temperature (800-1150 K) in the pressure range 1 to 10 arm for several equivalence ratios (0.5 < ~b < 2). The concentration profiles of 02, H2, CO, CO2, CH4, C2H2, C2H4, C2H6, C3H6, C3H8, CH3HCO, and C2H40

Formation of H-atoms in the pyrolysis of
✍ Sebastian Peukert; Clemens Naumann; Marina Braun-Unkhoff; Uwe Riedel 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 647 KB

## Abstract Cyclohexane (cC~6~H~12~) plays an important role in the combustion of practical liquid fuels, as a major component of naphthenic compounds. Therefore, the pyrolysis of cyclohexane was investigated by measuring the formation of H‐atoms. The thermal decomposition of 1‐hexene (1‐C~6~H~12~)

Experimental study of the oxidation of n
✍ Philippe Dagaut; Marcelline Reuillon; Michel Cathonnet 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 875 KB

Normal heptane oxidation in a high-pressure jet-stirred reactor has been investigated experimentally in a wide range of conditions covering the low-and high-temperature oxidation regimes (550-1150 K, l-40 atm, I#J = 1). Reactants, intermediates, and final products have been measured in three differe