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Kinetics of the polymerization of alkenes on zeolites

Journal Article · · J. Chem. Phys.; (United States)
DOI:https://doi.org/10.1063/1.452963· OSTI ID:6295679

The polymerization of alkenes at temperatures in the neighborhood of 600 K on a zeolite catalyst can be described in terms of a mechanism with bimolecular polymerization reactions and cracking reactions of isomer groups. The rate equations for the formation of isomer groups up to C13H26 have been integrated using the fourth-order Runge--Kutta method for polymerizations at constant temperature and pressure. In the absence of data on rate constants, calculations have been made on the basis of the assumption that all the bimolecular rate constants are equal or all the cracking constants are equal. In each case the rate constants for the reverse reactions have been calculated using the equilibrium constants for the steps in the mechanism. Under some circumstances the plots of weight fractions of isomer groups vs time have nearly the same shape for the two assumptions. However, it is possible to distinguish between the two assumptions by using experiments at sufficiently high pressures. The calculations show that it is of interest to examine the compositions arising from different starting materials, even though the equilibrium composition depends only upon temperature and pressure.

Research Organization:
Chemistry Department, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139
OSTI ID:
6295679
Journal Information:
J. Chem. Phys.; (United States), Journal Name: J. Chem. Phys.; (United States) Vol. 87:6; ISSN JCPSA
Country of Publication:
United States
Language:
English