Mechanical Properties of End-Linked PEG/PDMS Hydrogels

被引:92
作者
Cui, Jun [1 ]
Lackey, Melissa A. [1 ]
Tew, Gregory N. [1 ]
Crosby, Alfred J. [1 ]
机构
[1] Univ Massachusetts, Dept Polymer Sci & Engn, Amherst, MA 01003 USA
基金
美国国家科学基金会;
关键词
DOUBLE-NETWORK HYDROGELS; POLYMER NETWORKS; STATISTICAL-MECHANICS; FRACTURE ENERGY; LARGE-STRAIN; STRENGTH; GELS; PERFORMANCE; BEHAVIOR; IMPACT;
D O I
10.1021/ma300593g
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理];
摘要
Poly(ethylene glycol) (PEG)/polydimethylsiloxane (PDMS) hydrogels were synthesized by cross-linking norbornene end-functionalized polymers with a tetrafunctional thiol using thiol-norbornene chemistry. The swelling capacity and mechanical properties, including the Young's modulus (E) and fracture toughness (G(c)), of the hydrogels were characterized and quantified as a function of the volume fractions of PEG and PDMS. E and G(c) increased simultaneously with the volume fraction of PDMS. The moduli of the hydrogels were quantitatively described and predicted as a function of the volume fraction ratio of PEG to PDMS using the Voigt and Reuss models. The fracture toughness was well described by the Lake-Thomas theory at low volume fractions of PDMS. As the volume fraction of PDMS increased, PDMS the hydrogels but also contributed to hydrogel toughness. not only controlled the swelling capacity of the hydrogels but also contributed to hydrogel toughness.
引用
收藏
页码:6104 / 6110
页数:7
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