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Effect of high polymerization temperature on the microstructure of isotactic polypropylene prepared using heterogeneous TiCl4/MgCl2 catalysts

机译:聚合温度高对多相TiCl4 / MgCl2催化剂制备的等规聚丙烯微观结构的影响

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摘要

The effects of alkylaluminum and polymerization temperature on propylene polymerization without an external donor in the use of a TiCl4-MgCl2-diether(BMMF) catalyst were investigated. The results indicated that with increasing polymerization temperature the concentrations of [mmmm] of heptane-insoluble poly(propylene) (PP) fraction increased. Crystallization analysis fractionation (CRYSTAF) results showed the fractions of different crystallization temperatures were changed according to various polymerization temperatures. The activity with Et3Al as cocatalyst at 100degreesC was much lower than that at 70degreesC. However, the activity with i-Bu3Al at 100degreesC was as high as that at 70degreesC. The fraction of high-crystallization temperature of PPs obtained with i-Bu3Al increased with increasing polymerization temperature, which was opposite to that with Et3Al, thus implying that the copolymerization of propylene with the monomer arising from Et3Al led to the lower crystallization ability of PPs obtained with Et3Al. The terminal groups of PP suggested that the chain-transfer reaction by beta-H abstraction was the main chain-transfer reaction at 120degreesC. (C) 2003 Wiley Periodicals, Inc. [References: 14]
机译:研究了在使用TiCl4-MgCl2-二醚(BMMF)催化剂的情况下,烷基铝和聚合温度对丙烯聚合反应的影响。结果表明,随着聚合温度的升高,庚烷不溶性聚丙烯(PP)馏分的[mmmm]浓度增加。结晶分析分级分离(CRYSTAF)结果表明,不同结晶温度的馏分随聚合温度的变化而变化。以Et3Al为助催化剂在100℃时的活性远低于70℃时的活性。但是,i-Bu3A1在100℃下的活性与70℃下一样高。用i-Bu3Al制备的PPs的高结晶温度分数随聚合温度的升高而增加,这与Et3Al的相反,这表明丙烯与Et3Al产生的单体的共聚反应导致所得PPs的结晶能力降低。与Et3Al。 PP的末端基团表明,通过β-H提取的链转移反应是120℃下的主要链转移反应。 (C)2003 Wiley Periodicals,Inc. [参考:14]

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