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Functional copolymer/organo‐MMT nanoarchitectures. III. Dynamic mechanical behavior of poly(IA‐ co ‐BMA)‐organo‐MMT clay nanocomposites
Author(s) -
Rzayev Zakir M. O.,
Güner Ali,
Söylemez Ernur A.,
Kavlak Serap
Publication year - 2011
Publication title -
polymers for advanced technologies
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.61
H-Index - 90
eISSN - 1099-1581
pISSN - 1042-7147
DOI - 10.1002/pat.1618
Subject(s) - copolymer , materials science , exfoliation joint , nanocomposite , montmorillonite , comonomer , intercalation (chemistry) , polymer chemistry , chemical engineering , methacrylate , polymer , composite material , graphene , organic chemistry , chemistry , nanotechnology , engineering
Functional copolymer/organo‐silicate [ N , N ′‐dimethyldodecyl ammonium cation surface modified montmorillonite (MMT)] layered nanocomposites have been synthesized by interlamellar complex‐radical copolymerization of pre‐intercalated itaconic acid (IA)/organo‐MMT complex as a “nanoreactor” with n ‐butyl methacrylate (BMA) as an internal plasticization comonomer in the presence of radical initiator. Comparative analysis of physical structure, dynamic mechanical analysis parameters, and surface morphology of the obtained copolymers and their nanocomposites indicated that the interlayer H‐bonding and flexible n ‐butyl ester linkages take place an important role in interlamellar copolymerization and intercalation/exfoliation of copolymer chains. It was found that nanocomposites' dynamic mechanical properties strongly depended on the force of interfacial H‐bonding and amount of BMA units. An increase in both of these parameters leads to enhanced intercalation and exfoliation in situ processes of copolymer chains and the formation of hybrid nanocomposites. Copyright © 2009 John Wiley & Sons, Ltd.