Correlation between catalyst surface structure and polypropylene tacticity in Ziegler-Natta polymerization system

被引:33
作者
Kim, SH
Somorjai, GA [1 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Lawrence Berkeley Lab, Div Mat Sci, Berkeley, CA 94720 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2001年 / 105卷 / 18期
关键词
D O I
10.1021/jp002997y
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
correlation between the surface structure of the Ziegler-Natta catalysts and the stereospecificity in propylene polymerization was shown experimentally using model catalysts and temperature-programmed desorption (TPD) of mesitylene as a nondestructive surface probe. Two types of titanium chloride model catalysts, with MgCl2 support (TiClx/MgCl2) and without MgCl2 (TiCly), were fabricated on an Au substrate in ultrahigh vacuum. Once activated with AIEt(3) vapor, both catalysts were active for propylene polymerization in the absence of excess ALEt(3) during polymerization. The TiClx/MgCl2 catalyst produced both atactic and isotactic polypropylene, while the TiCly catalyst without the MgCl2 support produced exclusively isotactic polypropylene. For the same catalysts, the mesitylene TPD revealed that TiClx/MgCl2 had two adsorption site structures, a basal plane structure and a nonbasal plane structure, while TICly had only the latter structure. To our knowledge, this was the first direct experimental evidence revealing the structural difference of the catalyst surfaces that exhibit different stereospecificity in propylene polymerization.
引用
收藏
页码:3922 / 3927
页数:6
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