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揭示 Ti(3+) 和 Al(3+) 位点在氯化 Al2 O3 上的协同催化作用:支化聚乙烯的串联方法。

Unraveling the Catalytic Synergy between Ti(3+) and Al(3+) Sites on a Chlorinated Al2 O3 : A Tandem Approach to Branched Polyethylene.

机构信息

Department of Chemistry-INSTM and NIS Centre, University of Torino, via Giuria 7, 10125, Torino, Italy.

出版信息

Angew Chem Int Ed Engl. 2016 Sep 5;55(37):11203-6. doi: 10.1002/anie.201604136. Epub 2016 Jul 21.

Abstract

An original step-by-step approach to synthesize and characterize a bifunctional heterogeneous catalyst consisting of isolated Ti(3+) centers and strong Lewis acid Al(3+) sites on the surface of a chlorinated alumina has been devised. A wide range of physicochemical and spectroscopic techniques were employed to demonstrate that the two sites, in close proximity, act in a concerted fashion to synergistically boost the conversion of ethylene into branched polyethylene, using ethylene as the only feed and without any activator. The coordinatively unsaturated Al(3+) ions promote ethylene oligomerization through a carbocationic mechanism and activate the Ti(3+) sites for the traditional ethylene coordination polymerization.

摘要

设计了一种新颖的分步方法,用于合成和表征一种双功能异质催化剂,该催化剂由氯化氧化铝表面上的孤立 Ti(3+)中心和强路易斯酸 Al(3+)位组成。采用多种物理化学和光谱技术证明,这两个紧密相邻的位点以协同方式协同作用,在没有任何活化剂的情况下,仅使用乙烯作为唯一进料,将乙烯转化为支化聚乙烯。配位不饱和的 Al(3+)离子通过碳阳离子机理促进乙烯齐聚,并激活 Ti(3+)位进行传统的乙烯配位聚合。

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