Novel organic/inorganic support for immobilizing TiCl3/(n-BuCp)2ZrCl2 catalyst to prepare wide distribution polyethylene
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Novel organic/inorganic support for immobilizing TiCl3/(n-BuCp)2ZrCl2 catalyst to prepare wide distribution polyethylene
CIESC JournalIssue 5, Pages: 1127-1136(2010)
作者机构:
1. 化学工程联合国家重点实验室,浙江大学化学工程与生物工程学系
2. 中国石油化工股份有限公司天津分公司
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Online First:05 May 2010,
Published:05 May 2010
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LI Wei, WU Jing, DU Lijun, et al. Novel organic/inorganic support for immobilizing TiCl3/(n-BuCp)2ZrCl2 catalyst to prepare wide distribution polyethylene[J]. CIESC Journal, 2010, (5): 1127-1136.
DOI:
LI Wei, WU Jing, DU Lijun, et al. Novel organic/inorganic support for immobilizing TiCl3/(n-BuCp)2ZrCl2 catalyst to prepare wide distribution polyethylene[J]. CIESC Journal, 2010, (5): 1127-1136.DOI:
Novel organic/inorganic support for immobilizing TiCl3/(n-BuCp)2ZrCl2 catalyst to prepare wide distribution polyethylene
A novel organic/inorganic support for immobilizing a hybrid catalyst used in ethylene polymerization was devised.The composition of the hybrid catalyst was as follows:styrene and acrylic copolymer (PSA) was the organic part for binding (n-BuCp)2ZrCl2
and SiO2/MgCl2 was the inorganic part to immobilize TiCl3.As an alternative to a tandem or cascade type process
a two-step polymerization method was carried out in a single reactor on a laboratory scale.Utilizing this two-step polymerization process
reactor blends of high molecular weight (made in the first step) copolymer and low molecular weight homo-polymer (made in the second step) were produced that were similar to industrial resins.The results showed that polymer blends had bimodal molecular weight distribution and broad melt flow rate (MI21.6/MI2.16=79).Besides
the melting point and crystallinity of the blends were in the range of polymers made separately in the first and second polymerization steps
indicating that the polymer obtained by the hybrid catalyst had good co-crystallinity.Catalyst kinetic curves in each polymerization step showed that the introduction of PSA facilitated gradual generation of the active sites of catalyst.Thus
the activity could be maintained in a long time in each polymerization step.