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Aminolysis reaction of poly( N ‐4‐methylphenylitaconimide) and its graft copolymerization
Author(s) -
Qiu Kun Yuan,
Zhao Tong
Publication year - 1995
Publication title -
polymer international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.592
H-Index - 105
eISSN - 1097-0126
pISSN - 0959-8103
DOI - 10.1002/pi.1995.210380109
Subject(s) - copolymer , aminolysis , polymer chemistry , ethyl acrylate , materials science , polymer , acrylate , methyl acrylate , chemistry , organic chemistry , catalysis , composite material
Polyitaconimide and copolymers of itaconimide were transformed to macromolecules having diamido pendent groups via an aminolysis reaction. The polymers obtained were cast into films, which were then graft copolymerized with acrylamide (AAM) using ceric ion as an initiator. Radical homopolymerization and copolymerization of N ‐4‐methylphenylitaconimide with methyl acrylate or ethyl acrylate were carried out at 60°C in benzene; high molecular weight polymer and copolymers (M̄ n = 10 4 –10 5 ) were obtained. The resulting polymer and copolymers were reacted with n ‐butylamine in order to produce polymers possessing a pendent 4‐tolylcarbamoyl group (4‐CH 3 C 6 H 4 NHCO‐), which can significantly promote the acrylamide (AAM) graft copolymerization initiated with ceric ion. Transparent films of the polymers were graft copolymerized with AAM in the presence of ceric ion at 45°C. The formation of graft polymers was verified by water absorption percentage, XPS and SEM.

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