1998
DOI: 10.1016/s1381-1169(97)00175-1
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Influence of metallocene structures on ethene copolymerization with 1-butene and 1-octene

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Cited by 95 publications
(71 citation statements)
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“…The activity of 7 increased at high temperature, especially at 50 • C, and no significant differences in the T g values (NBE content) in the resultant copolymers were observed by varying the temperature (25-70 • C). This would suggest that there has not been a significant temperature dependence observed for the NBE incorporation, as has been observed in ethylene/α-olefin copolymerization by ordinary ansa metallocene catalysts [68,69]. Scheme 4.…”
Section: Copolymerization Of α-Olefin With Norbornene (Nbe) or Tetracmentioning
confidence: 90%
“…The activity of 7 increased at high temperature, especially at 50 • C, and no significant differences in the T g values (NBE content) in the resultant copolymers were observed by varying the temperature (25-70 • C). This would suggest that there has not been a significant temperature dependence observed for the NBE incorporation, as has been observed in ethylene/α-olefin copolymerization by ordinary ansa metallocene catalysts [68,69]. Scheme 4.…”
Section: Copolymerization Of α-Olefin With Norbornene (Nbe) or Tetracmentioning
confidence: 90%
“…[4] Consequently, an inverse relationship between the comonomer content and copolymer molecular weight is obtained, which is explained by kinetic reasons and implies a broad distribution of comonomer content in the copolymer. [5] This characteristic of the Ziegler-Natta systems makes the detailed study of the effect of comonomer incorporation on the final properties of the polymer difficult.…”
Section: Introductionmentioning
confidence: 97%
“…Usually butene, hexene, or octene are used as comonomers, but also longer olefins were utilized in recent years as comonomers, although such copolymers are not commercially available yet [4][5][6][7][8]. Another advantage of the single-site catalysts are their tendency to produce samples with a very homogeneous comonomer incorporation, which is not given for materials synthesized with ZN-catalysts or via the high pressure process [9][10][11]. By choosing a proper single-site catalyst and synthesis conditions, it is also possible to adjust the molar mass to almost any desired level with a narrow molar mass distribution (M w /M n =2) [12].…”
Section: Introductionmentioning
confidence: 99%