Effect of supported MAO cocatalysts in ethylene polymerization and ethylene/1-hexene copolymerization using Cp*TiCl2(O-2,6-iPr2C6H3) catalyst

被引:5
作者
Unruean, Palawat [1 ,2 ]
Apisuk, Wannida [3 ]
Kawabata, Youhei [3 ]
Murayama, Toni [3 ]
Kitiyanan, Boonyarach [1 ,2 ]
Nomura, Kotohiro [3 ]
机构
[1] Chulalongkorn Univ, Petr & Petrochem Coll, Soi Chulalongkorn 12,Phayathai Rd, Bangkok 10330, Thailand
[2] Chulalongkorn Univ, Ctr Excellence Petrochem & Mat Technol, Res Bldg,Soi Chulalongkorn 12,Phayathai Rd, Bangkok 10330, Thailand
[3] Tokyo Metropolitan Univ, Fac Sci, Dept Chem, 1-1 Mincuni Osawa, Hachioji, Tokyo 1920397, Japan
基金
日本学术振兴会;
关键词
Titanium; Supported catalyst; Ethylene polymerization; MAO; Half-titanocenes; NONBRIDGED HALF-TITANOCENES; OLEFIN POLYMERIZATION; (CYCLOPENTADIENYL)(ARYLOXY)TITANIUM(IV) COMPLEXES; MONOMER REACTIVITIES; DONOR LIGANDS; CYCLOPENTADIENYL; METALLOCENES; SUBSTITUENTS; ARYLOXO;
D O I
10.1016/j.mcat.2019.110490
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Ethylene slurry polymerization using Cp*TiCl2(O-2,6-(Pr2C6H3)-Pr-i) in the presence of supported solid MAO cocatalysts proceeded without decreasing in the activity compared to the homogeneous system, affording polymers with controlled shape replicated from the original support. Unique characteristics by 1 in the ethylene/1-hexene copolymerization observed in the homogeneous system (high catalytic activity, efficient 1-hexene incorporation, temperature dependence) have also been preserved in this catalysis, affording high molecular weight poly(ethylene-co-1-hexene)s with unimodal molecular weight distributions as well as with high 1-hexene contents.
引用
收藏
页数:8
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