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High activity mixed metal alkyl cocatalysts for α‐olefin polymerization

机译:用于α烯烃聚合的高活性混合金属烷基助催化剂

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AbstractHigh activity α‐olefin polymerization catalysts are generally obtained by mixing MgCl2‐supported TiCl4(MgCl2/TiCl4) with an aluminum trialkyl cocatalyst. Surprisingly, AlEt2Cl, which is the preferred cocatalyst in polymerizations employing nonsupported Ti compounds, is a poor cocatalyst when used with MgCl2/TiCl4. It was found that in propylene and 1‐butene polymerizations, using different MgCl2/TiCl4catalysts, the cocatalyst activity of AlEt2Cl can be greatly improved by the addition of a magnesium or lithium alkyl. The mixed metal alkyl obtained from AlEt2Cl and MgBu2is a particularly effective cocatalyst always yielding more polymer, of about the same stereospecificity, than the conventional aluminum trialkyls. The exact nature of the mixed metal alkyl cocatalysts is not known, but the available evidence argues against in situ aluminum trialkyl formation resulting from the alkylation of AlEt2Cl by the second metal
机译:摘要 将MgCl2负载的TiCl4(MgCl2/TiCl4)与三烷基铝助催化剂混合,可制得高活性α烯烃聚合催化剂。令人惊讶的是,AlEt2Cl 是采用非负载 Ti 化合物聚合的首选助催化剂,当与 MgCl2/TiCl4 一起使用时,它是一种较差的助催化剂。研究发现,在丙烯和1-丁烯聚合反应中,使用不同的MgCl2/TiCl4催化剂,通过添加镁或烷基锂可以大大提高AlEt2Cl的助催化剂活性。从AlEt2Cl和MgBu2获得的混合金属烷基是一种特别有效的助催化剂,总是比传统的三烷基铝产生更多的聚合物,具有大致相同的立体特异性。混合金属烷基助催化剂的确切性质尚不清楚,但现有证据反对第二种金属AlEt2Cl烷基化导致原位形成铝三烷基

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