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Evolution of high-temperature molecular relaxations in poly(2-(2-methoxyethoxy)ethyl methacrylate) upon network formation.


ABSTRACT: Copolymers of 2-(2-methoxyethoxy)ethyl methacrylate (poly(MEO2MA)) are regarded as bioinert replacements of poly(N-isopropylacrylamide) in some biomedical applications. Networks of poly(MEO2MA) of various architecture form thermo-responsive hydrogels. Here, we present dielectric and mechanical spectroscopy studies on segmental motions and network relaxation processes in linear poly(MEO2MA) and its networks - bare network and the network grafted with short poly(MEO2MA) chains. We show that the α process assigned to the segmental motions of poly(MEO2MA) is independent on the polymer topology and the glass transition temperature, Tg, associated with this process equals 235-236 K for all investigated systems. The α' relaxation observed above Tg by dynamical mechanical analysis is assigned to the sub-Rouse process. It strongly depends on the polymer network architecture and slows down by four orders of magnitude upon network formation.

SUBMITTER: Kozanecki M 

PROVIDER: S-EPMC4544547 | biostudies-literature | 2015

REPOSITORIES: biostudies-literature

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Evolution of high-temperature molecular relaxations in poly(2-(2-methoxyethoxy)ethyl methacrylate) upon network formation.

Kozanecki Marcin M   Pastorczak Marcin M   Okrasa Lidia L   Ulanski Jacek J   Yoon Jeong Ae JA   Kowalewski Tomasz T   Matyjaszewski Krzysztof K   Koynov Kaloian K  

Colloid and polymer science 20150130 5


Copolymers of 2-(2-methoxyethoxy)ethyl methacrylate (poly(MEO<sub>2</sub>MA)) are regarded as bioinert replacements of poly(<i>N</i>-isopropylacrylamide) in some biomedical applications. Networks of poly(MEO<sub>2</sub>MA) of various architecture form thermo-responsive hydrogels. Here, we present dielectric and mechanical spectroscopy studies on segmental motions and network relaxation processes in linear poly(MEO<sub>2</sub>MA) and its networks - bare network and the network grafted with short  ...[more]

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