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Hydrogen and comonomer effects on Ziegler-Natta catalyzed propylene polymerization using different types of alkoxysilane external donor

机译:使用不同类型的烷氧基硅烷外部供体对Ziegler-Natta催化丙烯聚合的氢气和共聚单体效应

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Alkoxysilanes are the most commercially used external donor in propylene polymerization using Ziegler-Natta (ZN) catalyst. It is known that the molecular structure of alkoxysilane such as the number and size of alkoxy groups as well as the size of alkyl groups attached to the silicon atom affects the catalyst performance[l]. However the systematic establishment of structure-performance relationship (SPR) for various types of alkoxysilane has not been satisfactory acquired, especially under different polymerization conditions. In our previous work, the relationship between polymerization performances in stopped-flow (SF) and slurry polymerization and alkoxysilane structures was compared with the calculated active site performances based on coadsorption model. It was found that an alkoxysilane adsorbed strongly on MgCl2 surfaces tended to give a higher polymer yield and the conformation detail of alkyl structures around active sites was essential for stereospecificity improvement[2]. In the present study, the effects of alkoxysilane structures on the comonomer incorporation and the hydrogen response in propylene polymerization were investigated, aiming at the SPR information of alkoxysilane structures for the further development of new donor system.
机译:烷氧基硅烷是使用齐格勒 - 纳塔(ZN)催化剂在丙烯聚合的最商业上使用的外部给体。已知的是,烷氧基硅烷等的烷氧基基团的数目和大小以及连接至硅原子的烷基基团的大小的分子结构影响催化剂性能[1]。然而的结构 - 性能关系(SPR)的各类烷氧基硅烷的系统的建立还没有令人满意的获取,特别是在不同的聚合条件。在我们以前的工作,在停流(SF)和淤浆聚合和烷氧基硅烷结构聚合性能之间的关系是基于共吸附模型计算出的活性位点的演出相比。据发现,烷氧基硅烷在MgCl 2上牢固地吸附表面倾向于得到较高的聚合物产率和烷基结构围绕活性位点是为改善立体定向性[2]基本的构象细节。在本研究中,对共聚单体引入和在丙烯聚合中的氢烷氧基硅烷反应的结构的效果进行了研究,目的在于烷氧基硅烷结构的新的供体系统的进一步发展的SPR信息。

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