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Homogeneous gas‐phase pyrolyses with a wall‐less reactor. III. The oxygen–ethane reaction. A double reversal in oxygen and surface effects
Author(s) -
Taylor Jay E.,
Kulich Donald M.
Publication year - 1973
Publication title -
international journal of chemical kinetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.341
H-Index - 68
eISSN - 1097-4601
pISSN - 0538-8066
DOI - 10.1002/kin.550050314
Subject(s) - chemistry , oxygen , homogeneous , pyrolysis , photochemistry , radical , reaction rate , inorganic chemistry , catalysis , organic chemistry , thermodynamics , physics
The impact of surface and oxygen on the oxidative pyrolysis of ethane at temperatures above 590°C was studied using a wall‐less reactor. At very low conversions under homogeneous conditions, ethene formation begins at the same temperature regardless of whether oxygen is present or absent. Between 0.00 and 0.13% conversion (592–632°C), the rate with oxygen is actually less than the rate in the absence of oxygen. A reversal occurs at about 633°C above which oxygen has a promoting effect. It is concluded that under homogeneous conditions the initiation step in the oxygen‐promoted pyrolysis is the same as in the oxygen‐free pyrolysis; therefore, initiation by direct attack of oxygen on ethane does not make an important contribution. The decrease in rate observed upon addition of oxygen implies the formation of the relatively unreactive HO 2 · radical. As conversion of the HO 2 · radical to the more reactive HO · radical becomes significant, the reaction is highly accelerated. If a stainless steel surface is added, the reaction is inhibited at higher conversions in the presence of oxygen. Again at low conversions, a second reversal occurs, and the stainless steel surface acts as a promoter below 649°C. The rate of surfacecatalyzed ethene formation at 590°C equals the rate of homogeneous ethene formation at 630°C.