Viscoelastic Properties of Supramolecular Soft Materials with Transient Polymer Network

被引:30
|
作者
Hayashi, Mikihiro [1 ]
Noro, Atsushi [1 ]
Matsushita, Yushu [1 ]
机构
[1] Nagoya Univ, Grad Sch Engn, Dept Appl Chem, Chikusa Ku, Nagoya, Aichi 4648603, Japan
关键词
hydrogen bonding; rheology; supramolecular soft materials; transient network; X-ray scattering; SUPRAMACROMOLECULAR ION GELS; GELATION MECHANISM; THERMOREVERSIBLE GELATION; NANOCOMPOSITE HYDROGELS; INCLUSION COMPLEXATION; RHEOLOGICAL BEHAVIOR; TRIBLOCK COPOLYMER; MOLECULAR-SIZE; DYNAMICS; TRANSITION;
D O I
10.1002/polb.23479
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A series of supramolecular soft materials with hydrogen bonded transient networks was prepared by blending carboxy-terminated telechelic poly(ethyl acrylate) (PEA-(COOH)(2)) and polyethyleneimine (PEI). Effects of PEA-(COOH)(2) molecular weight (M-PEA) and the blend ratio on the viscoelastic properties were investigated by rheological and small angle X-ray scattering measurements. Rubbery plateau appeared by adding PEI due to network formation with ionic hydrogen bonded crosslinks between amines on PEI and carboxylic acids on PEA-(COOH)(2). The highest temperature of a storage modulus-loss modulus crossover as well as the highest flow activation energy was attained at a certain mole ratio of amines to carboxylic acids, irrelevant to M-PEA, indicating optimized supramolecular networks were achieved by stoichiometric balance of two functional groups. Since telechelic PEA-(COOH)(2) serves as a network strand, the plateau modulus was inversely proportional to M-PEA, which was consistent with the correlation length between crosslinks estimated by X-ray scattering measurements. (c) 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2014, 52, 755-764
引用
收藏
页码:755 / 764
页数:10
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