Kinetic study of ethylene polymerization with chromium oxide catalysts by a radiotracer technique

The quenching of polymerization with a chromium oxide catalyst by radioactive methanol 14 CH 3 OH enables one to determine the concentration of propagation centers and then to calculate the rate constant of the propagation. The dependence of the concentration of propagation centers and the polymeriz...

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Veröffentlicht in:Journal of polymer science. Part A-1, Polymer chemistry Polymer chemistry, 1971-11, Vol.9 (11), p.3129-3146
Hauptverfasser: Zakharov, V. A., Ermakov, Yu. I.
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container_issue 11
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container_title Journal of polymer science. Part A-1, Polymer chemistry
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creator Zakharov, V. A.
Ermakov, Yu. I.
description The quenching of polymerization with a chromium oxide catalyst by radioactive methanol 14 CH 3 OH enables one to determine the concentration of propagation centers and then to calculate the rate constant of the propagation. The dependence of the concentration of propagation centers and the polymerization rate on reaction time, ethylene concentration, and temperature was investigated. The change of the concentration of propagation centers with the duration of polymerization was found to be responsible for the time dependence of the overall polymerization rate. The propagation reaction is of first order on ethylene concentration in the pressure range 2–25 kg/cm 2 . For catalysts of different composition, the temperature dependence of the overall polymerization rate and the propagation rate constant were determined, and the overall activation energy E ov and activation energy of the propagation state E p were calculated. The difference between E ov and E p is due to the change of the number of propagation centers with temperature. The variation of catalyst composition and preliminary reduction of the catalyst influence the shape of the temperature dependence of the propagation center concentration and change E ov .
doi_str_mv 10.1002/pol.1971.150091104
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title Kinetic study of ethylene polymerization with chromium oxide catalysts by a radiotracer technique
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