Temperature effect on the kinetic profile of Ziegler-Natta catalyst in propene polymerization

Abstract

Propene polymerization kinetic profiles with a diether-based Ziegler-Natta MgCl2-supported catalyst were investigated in a stainless-steel batch reactor. The initial 10 min period characterizes various temperature levels with a constant volume of liquid propene. The lowest temperature level corresponds to the usual prepolymerization temperature (10 degrees C), and the highest level corresponds to the usual main polymerization temperature (70 degrees C). The effects of the starting temperature levels were evaluated through polymerization kinetic patterns computed namely from the second polymerization period carried out at 70 degrees C for the next 90 min. Based on the heat transfer data, the kinetic profiles were fitted to suitable semi-empirical equations derived from fundamental kinetic approaches using the first and second orders of the catalyst active sites decay. Both approaches adequately describe the dependence of the initial activities and deceleration constants on the temperature during the initial period.Propene polymerization kinetic profiles with a diether-based Ziegler-Natta MgCl2-supported catalyst were investigated in a stainless-steel batch reactor. The initial 10 min period characterizes various temperature levels with a constant volume of liquid propene. The lowest temperature level corresponds to the usual prepolymerization temperature (10 degrees C), and the highest level corresponds to the usual main polymerization temperature (70 degrees C). The effects of the starting temperature levels were evaluated through polymerization kinetic patterns computed namely from the second polymerization period carried out at 70 degrees C for the next 90 min. Based on the heat transfer data, the kinetic profiles were fitted to suitable semi-empirical equations derived from fundamental kinetic approaches using the first and second orders of the catalyst active sites decay. Both approaches adequately describe the dependence of the initial activities and deceleration constants on the temperature during the initial period.