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Ethylene polymerization, with Lewis acid catalytic activity

The sterically encumbered R2 substituents give steric protection to the oxygen-donors that are attached to the metal centers from coordination with Lewis acids such as MAO, or from another molecule of the catalytically active cationic species, which are supposed to be highly electrophilic. The coordination increases steric congestion near the polymerization center, which at least hampers ethylene coordination to the metal. Even worse, it may cause catalyst decay by, for instance, loss of the ligand. [Pg.14]

A patent for the polymerization process of olefins (especially ethylene, a-olefins, cyclopentene, and some fluorlnated olefins) describes the above catalytic systems [20]. The hindered diimines stabilize alkyl Ni(ll) or Pd(n) with cationic complexes. After preparation, the complexes are reduced with methylalu-minoxane and then activated with Lewis acids capable of forming non-coordinating counterions [20]. [Pg.333]

The catalytic work on the zeolites has been carried out using the pulse microreactor technique (4) on the following reactions cracking of cumene, isomerization of 1-butene to 2-butene, polymerization of ethylene, equilibration of hydrogen-deuterium gas, and the ortho-para hydrogen conversion. These reactions were studied as a function of replacement of sodium by ammonium ion and subsequent heat treatment of the material (3). Furthermore, in some cases a surface titration of the catalytic sites was used to determine not only the number of sites but also the activity per site. Measurements at different temperatures permitted the determination of the absolute rate at each temperature with subsequent calculation of the activation energy and the entropy factor. For cumene cracking, the number of active sites was found to be equal to the number of sodium ions replaced in the catalyst synthesis by ammonium ions up to about 50% replacement. This proved that the active sites were either Bronsted or Lewis acid sites or both. Physical defects such as strains in the crystals were thus eliminated and the... [Pg.136]


See other pages where Ethylene polymerization, with Lewis acid catalytic activity is mentioned: [Pg.781]    [Pg.104]    [Pg.187]    [Pg.215]    [Pg.309]    [Pg.504]    [Pg.726]    [Pg.117]    [Pg.57]    [Pg.119]    [Pg.10]    [Pg.144]    [Pg.235]    [Pg.10]    [Pg.5762]    [Pg.922]    [Pg.562]    [Pg.678]    [Pg.154]    [Pg.287]    [Pg.383]   


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Acidic catalytic activity

Activated polymerization

Activator polymerization

Ethylene acidity

Ethylene acids

Ethylene polymerization

Ethylene polymerization, with Lewis acid

Lewis acid-activators

Lewis acids activity

Lewis acids, polymeric

Polymerization activity

Polymerization, activation

Polymerization, with

With Lewis Acids

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