Molecular dynamics in PBA/PEO miktoarm star copolymers

被引:5
作者
Makrocka-Rydzyk, Monika [1 ]
Wypych, Aleksandra [2 ]
Dobies, Maria [1 ]
Jancelewicz, Mariusz [1 ,3 ]
Jurga, Stefan [1 ,3 ]
Cho, Hong Yul [4 ]
Gao, Haifeng [4 ]
Matyjaszewski, Krzysztof [4 ]
机构
[1] Adam Mickiewicz Univ, Dept Macromol Phys, Fac Phys, PL-61614 Poznan, Poland
[2] Lodz Univ Technol, Dept Mol Phys, Fac Chem, PL-90924 Lodz, Poland
[3] Adam Mickiewicz Univ, NanoBioMed Ctr, PL-61614 Poznan, Poland
[4] Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA
基金
美国国家科学基金会;
关键词
Miktoarm star copolymers; Dielectric spectroscopy; NMR relaxometry; GLASS-TRANSITION; POLY(N-BUTYL ACRYLATE); RELAXATION PROCESSES; SEGMENTAL DYNAMICS; TEMPERATURE; CRYSTALLIZATION; VISCOSITY; FRAGILITY; POLYMERS; NMR;
D O I
10.1016/j.polymer.2013.04.004
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Molecular dynamics of miktoarm star copolymers consisting of poly(n-butyl acrylate) PBA and polyethylene oxide (PEO) arms was studied by means of Broadband Dielectric Spectroscopy (BDS) and Nuclear Magnetic Resonance (NMR) methods. The spectroscopic studies were performed for three types of copolymers differing in the composition, namely materials containing 76%, 46% and 16% molar fraction of PBA arms. The local processes, described by the Arrhenius law (e.g. the anisotropic rotation of methyl groups and the anisotropic local motions in the PEO chain), were observed for the studied systems below the glass transition temperature. It was found that the investigated PBA/PEO miktoarm star copolymers are characterized by single glass transition, which may result from similar values of glass transition temperatures of the PBA and PEO polymers. The segmental dynamics in the studied systems was quantitatively described by using the Vogel-Fulcher-Tammann (VFT) relation applied to combined NMR and BDS data. Moreover, above the glass transition temperature the interfacial polarization and conductivity phenomena were detected with the BDS method for all systems under study. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3341 / 3349
页数:9
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