Structure and physical properties of dried Tetra-PEG gel

被引:18
作者
Nomoto, Yusaku [1 ]
Matsunaga, Takuro [1 ]
Sakai, Takamasa [2 ]
Tosaka, Masatoshi [3 ]
Shibayama, Mitsuhiro [1 ]
机构
[1] Univ Tokyo, Inst Solid State Phys, Chiba 2778581, Japan
[2] Univ Tokyo, Sch Engn, Dept Bioengn, Bunkyo Ku, Tokyo 1138656, Japan
[3] Kyoto Univ, Inst Chem Res, Kyoto 6110011, Japan
关键词
Polymer gel; Polymer melt; Network structure; STRAIN-INDUCED CRYSTALLIZATION; HIGH MECHANICAL STRENGTH; LINKED POLYMER-CHAINS; X-RAY-DIFFRACTION; NATURAL-RUBBER; POLY(ETHYLENE OXIDE); SPATIAL INHOMOGENEITY; GELATION THRESHOLD; NETWORK STRUCTURE; MODEL NETWORKS;
D O I
10.1016/j.polymer.2011.06.053
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We investigated crystal structure, and thermal, swelling, and deformation behaviors of dried tetra-functional (polyethylene glycol) gel, Tetra-PEG gel, with narrow molecular distribution. Tetra-PEG gel consists of two kinds of symmetrical tetrahedron-like PEG macromonomers with a fixed molecular weight. In spite of network structure with rather small molecular weight between cross-links (M(c)) (approximate to 5000), the dried Tetra-PEG gels were found to be capable of crystallization. The crystalline melting temperature (T(m)) and the degree of crystallinity (X(c)) of dried Tetra-PEG gels obtained by differential scanning calorimetry (DSC) were substantially constant against the polymer volume fraction at preparation (phi(0)). Furthermore, the corrected elastic modulus (G) of dried Tetra-PEG gels did not depend on phi(0). These experimental results indicate that the there exist negligible entanglements in the dried Tetra-PEG network irrespective of phi(0). In other words, Tetra-PEG gels do not have significant topological inhomogeneities. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4123 / 4128
页数:6
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