Effect of MAO silica surface loading on (nBuCp)2ZrCl2 anchoring, on catalyst activity and on polymer properties

被引:28
作者
Bianchini, D [1 ]
Stedile, FC [1 ]
dos Santos, JHZ [1 ]
机构
[1] UFRGS, Inst Quim, BR-91509900 Porto Alegre, RS, Brazil
关键词
supported metallocene; MAO; silica; polymerization;
D O I
10.1016/j.apcata.2003.10.029
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
Silica Grace 948 activated at 723 K was modified with MAO in aluminum contents comprised between 0.5 and 20.0 wt.% Al/SiO2. Supported metallocene catalysts were prepared by grafting (nBuCp)(2)ZrCl2 toluene solutions directly onto silica and onto MAO-modified silicas. The catalysts were characterized by a series of complementary techniques, namely, Rutherford backscattering spectrometry (RBS), Diffuse-reflectance Fourier transform spectroscopy (DRIFTS), ultraviolet-visible spectroscopy (UV-Vis) and electron probe microanalysis (EPMA). MAO-mediated systems presented higher Zr content comparing to directly silica supported system. For the MAO-modified silica systems, Zr content increases up to 2.0-4.0 wt.% Al/SiO2 reaching 1.5 wt.% Zr/SiO2. As the aluminum content increases, metal loading decreases achieving 0.6 wt.% Zr/SiO2 for the supported catalyst having 20.0 wt.% Al/SiO2. All the systems were shown to be active in ethylene polymerization having MAO as cocatalyst. Higher activity were achieved with MAO-mediated systems having 2.0-4.0 wt.% Al/SiO2. The catalyst systems produced polyethylenes with high molecular weight and narrow molecular weight distribution. The preparative protocol was stepwisely monitored by DRIFTS. For lower MAO content (2.0 wt.% Al/SiO2) residual isolated silanol groups were thoroughly consumed or perturbed after (nBuCp)(2)ZrCl2 impregnation. (C) 2003 Elsevier B.V. All rights reserved.
引用
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页码:57 / 67
页数:11
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