Full Paper: Copolymerization of ethylene and 1-hexene was carried out with different catalysts: homogeneous Et[Ind] 2 ZrCl 2 , Cp 2 HfCl 2 and [(C 5 Me 4 )SiMe 2 N(tert-Bu)]TiCl 2 , the corresponding in-situ supported metallocenes, and combined in-situ supported metallocene catalysts (mixtures of Et
Molecular weight distribution of metallocene polymerization with long chain branching using a binary catalyst system
β Scribed by Shiping Zhu; Dean Li
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 482 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1022-1344
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β¦ Synopsis
Abstract
In metallocene polymerization, termination by Ξ²βhydride elimination generates polymer chains containing unsaturated vinyl groups at their chain ends. Further polymerization of these macromonomers produces branched polymers. Material properties of the branched polymers not only depend on molecular weight and branching density, but also on chain structure. This work presents analytical expressions to predict the bivariate distribution of molecular weight and branching density for polymer chains having dendritic and comb structures. It is shown that when a single metallocene catalyst is used the formation of dendritic polymers is favored with only a very small fraction of highly branched chains assuming comb structure. The use of a binary catalyst system is therefore proposed to obtain high content of comb polymers. One catalyst generates macromonomers and the other yields inβsitu branching. It is found that the comb polymers give much narrower molecular weight distributions than dendritic polymers with same branching densities.
π SIMILAR VOLUMES
Polymerization of ethylene in a CSTR using a combined metallocene catalyst system (combination of an open-face catalyst, such as Constrained Geometry Catalyst, and a conventional metallocene catalyst) was studied. Using the model developed by Soares and Hamielec, and expanded by Beigzadeh et al., a