MgCl2-supported TiCl4 catalysts containing diethyl norbornene-2,3-dicarboxylate internal electron donor for 1-butene polymerization: Effects of internal electron donor configuration
Three isomeric 5-norbornene-2,3-dicarboxylic acid diethyl ester (NDDE) with endo-, exo-, and trans-configuration have been synthesized and employed as internal electron donors (IED) in 1-butene polymerization over magnesium chloride supported Ziegler-Natta catalysts. It was found that the configurat...
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Published in | Journal of applied polymer science Vol. 131; no. 18; pp. 9192 - n/a |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken, NJ
Blackwell Publishing Ltd
15.09.2014
Wiley Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | Three isomeric 5-norbornene-2,3-dicarboxylic acid diethyl ester (NDDE) with endo-, exo-, and trans-configuration have been synthesized and employed as internal electron donors (IED) in 1-butene polymerization over magnesium chloride supported Ziegler-Natta catalysts. It was found that the configuration of NDDE plays a key role in tuning the catalyst activity, stereospecificity, molecular weight (MW), and polydispersity index (PDI) of resulting poly(1-butene). The type of catalyst with cis-5-norbornene-endo-2,3-dicarboxylic acid diethyl ester as IED shows the highest catalyst activity, while catalyst with trans-NDDE as IED yields the poly(1-butene) with the highest MW and the most broad PDI. IR results showed that the NDDE with endo-, exo-, and trans-configuration have different coordination way to MgCl2, subsequently affecting the catalysts performance. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014, 131, 40758. |
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Bibliography: | National Nature Science Foundation of China (NSFC) program - No. 51373046; No. 21004017 istex:43C4C778A033DF584EF4F827DA4AAB0CAF3DC252 ark:/67375/WNG-5QQCKCVL-X ArticleID:APP40758 Program for New Century Excellent Talents in University - No. NCET-10-0125 |
ISSN: | 0021-8995 1097-4628 |
DOI: | 10.1002/app.40758 |