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Zigler-Natta

Usually the Zigler-Natta co-ordination initiator system is used to graft oc-olefins onto other polymers to give stereo block/graft copolymers, which contain isotactic/atactic sequences. In the Zigler-Natta co-ordination catalyst [69] system, the diethyl aluminium hydride reacts with pendant groups to form macromolecular trialkyl aluminium. The residual initiator is freed by extraction methods. [Pg.242]

Most addition polymerizations involve vinyl or diene monomers. The opening of a double bond can be catalyzed in several ways. Free-radical polymerization is the most common method for styrenic monomers, whereas coordination metal catalysis (Zigler-Natta and metallocene catalysis) is important for olefin polymerizations. The specitic reaction mechanism may generate some catalyst residues, but there are no true coproducts. There are no stoichiometry requirements, and equilibrium limitations are usually unimportant so that quite long chains are formed 7iv > 500 is typical of addition polymers. [Pg.478]

Method of synthesis - addition polymerization polymerization occurs on contact of monomer with Zigler-Natta catalyst ... [Pg.286]


See other pages where Zigler-Natta is mentioned: [Pg.479]    [Pg.479]    [Pg.257]    [Pg.633]    [Pg.479]    [Pg.334]    [Pg.479]    [Pg.479]    [Pg.257]    [Pg.633]    [Pg.479]    [Pg.334]   
See also in sourсe #XX -- [ Pg.241 , Pg.245 ]




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