Abstract

The catalyst formed by the interaction of chromium (III) 2-ethylhexanoate or related compounds with partially hydrolyzed triisobutyl aluminum, in paraffinic solvents, polymerizes ethylene to linear polyethylene at ethylene turnover numbers of the order of 30 sec −1 atm −1. The polyethylene appears to be formed by what has come to be considered a conventional Ziegler olefin polymerization mechanism [Novaro et al., J. Catal. 41, 91 (1976)]. Hexene-1 can also be produced, at rates comparable to those of polyethylene formation. The mechanism of hexene-1 formation differs from that of polyethylene formation, as shown by differences in the pressure and temperature dependence of the two rates and by the inhibition of hexene-1 formation, but not polyethylene formation, by small quantities of dienes. Some mechanistic implications of the hexene-1 formation kinetics are discussed. Information relating to the structure of poly(isobutyl aluminum oxide) is also presented. Some structures for the catalytically active centers are proposed, and reactions by which such structures could be produced are suggested.

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