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Mechanism of propane oxidation–mathematical modeling

✍ Scribed by A. A. Levitsky; S. S. Polyak; V. Ya. Shtern


Publisher
John Wiley and Sons
Year
1984
Tongue
English
Weight
543 KB
Volume
16
Category
Article
ISSN
0538-8066

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✦ Synopsis


Mathematical modeling was used for the kinetics of gas-phase propane oxidation at 586,613, and 658 K and pressures 172 and 250 torr. The reaction mechanism involving branching by decay of the peracetyl peroxy radical, and oxygen-containing products formed on decay of the RO, radical is discussed. Fair agreement between calculated and experimental results on the kinetics and accumulation rates of reaction products was obtained.

The kinetics of gas-phase propane oxidation was studied earlier [l-51. The composition of products, the basic kinetic regularities, the compound (CH,CHO) responsible for degenerate chain branching were found. A reaction mechanism was suggested.

Experiments were conducted under static conditions in a reactionpretreated quartz reactor at 313, 340, and 385°C and 172 and 250 torr. Chromatographic analysis showed C3H6, CHzO, CH,OH, CH,CHO, C3H60, CO, COz, and HzO as the basic products, CzH4, CHI, CzHs, and CzH50H in smaller amounts, and traces of acetone. In the runs using the kinetic isotope method with addition of labeled propylene the products were analyzed for radioactivity.

Mathematical modeling is known to be a fairly effective method for analysis of the chemical reaction mechanisms with a view to assess the extent of their reliability. This refers in particular to the slow oxidation of alkanes [6-73.

The present article attempts generalization of the known experimental results for the kinetics of gas-phase propane oxidation by means of mathematical modeling. A seemingly most probable mechanism [2] is proposed, and its steps are analyzed.

The choice of the reaction mechanism of gas-phase propane oxidation involved two stages. The first consisted of selecting the basic steps * Institute of Petrochemical Synthesis.


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