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Charge-transfer mechanism, grafting

In the middle range of styrene concentrations, a compromise is attained where there is sufficient styrene to scavenge all excess methanol radicals not involved in activation of the trunk polymer, yet an excess of monomer remains for grafting by the charge-transfer mechanism proposed by Dilli and Garnett (12) originally for copolymerisation to cellulose (4) and subsequently extended to wool (3), polyolefin (2,5) and PVC (13) systems. The data in Table V are consistent with this interpretation. [Pg.255]

Thus in both radiation systems, monomer can diffuse to a site and graft by the charge-transfer mechanism previously proposed (3,5,15). [Pg.299]


See other pages where Charge-transfer mechanism, grafting is mentioned: [Pg.259]    [Pg.56]    [Pg.129]    [Pg.395]    [Pg.339]    [Pg.304]    [Pg.245]    [Pg.233]    [Pg.235]    [Pg.501]    [Pg.57]    [Pg.199]    [Pg.2085]    [Pg.373]    [Pg.93]   


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