A novel polymer-supported metallocene catalyst with crosslinked poly(styrene-co-acrylamide) (PSAm) as the support has been prepared and characterized. The probability of long sequences of acrylamide (Am) in PSAm is still low even at an Am amount of 32.8 mol %, implying the relatively homogeneous dis
Polymer-supported zirconocene catalyst for ethylene polymerization
β Scribed by Fenghua Meng; Guangqian Yu; Baotong Huang
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 184 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0887-624X
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β¦ Synopsis
The use of crosslinked poly(styrene-co-4-vinylpyridine) having functional groups as the support for zirconocene catalysts in ethylene polymerization was studied. Several factors affecting the activity of the catalysts were examined. Conditions like time, temperature, Al/N (molar ratio), Al/Zr (molar ratio), and the mode of feeding were found having no significant influence on the activity of the catalysts, while the state of the supports had a great effect on the catalytic behavior. The activity of the catalysts sharply increased with either the degree of crosslinking or the content of 4-vinylpyridine in the support. Via aluminum compounds, AlR 3 or methylaluminoxane (MAO), zirconocene was attached on the surface of the support. IR spectra showed an intensified and shifted absorption bands of CON in the pyridine ring, and a new absorption band appeared at about 730 cm Οͺ1 indicating a stable bond AlON formed in the polymer-supported catalysts. The formation of cationic active centers was hypothesized and the performance of the polymer-supported zirconocene was discussed as well.
π SIMILAR VOLUMES
In this paper we report on a zirconocene dichloride/methylaluminoxane catalyst system supported on a crosslinked polystyrene in order to provide ethylene polymerization catalysts for gas phase or slurry processes. Our novel approach uses the Diels-Alder reaction of cyclopentadiene functions as the f
Poly(styrene-co-acrylamide)(PSAm)-titanium complexes (PSAm \* Ti) were prepared and characterized. It is found that the coordination number of acrylamide (Am) to T i in the complexes is strongly dependent on Am content in PSAm, but not on [Am]/[Ti] ratio in the feed. The infrared and x-ray photoelec