Synthesis and thermomechanical behavior of (qua)ternary thiol-ene(/acrylate) copolymers

被引:16
作者
Kasprzak, Scott E. [1 ]
Martin, Blanton [2 ]
Raj, Tulika [3 ]
Gall, Ken [1 ]
机构
[1] Georgia Inst Technol, GWW Sch Mech Engn, Atlanta, GA 30322 USA
[2] Georgia Inst Technol, Dept Chem & Biochem, Atlanta, GA 30322 USA
[3] Georgia Inst Technol, Dept Biomed Engn, WHC, Atlanta, GA 30322 USA
关键词
Thiol-ene; Thermomechanics; Acrylate; METHACRYLATE TERNARY-SYSTEMS; THIOL-VINYL MECHANISMS; POLYMER NETWORKS; GLASS-TRANSITION; ENE; PHOTOPOLYMERIZATIONS; STEP; TEMPERATURE; HETEROGENEITY; CROSSLINKING;
D O I
10.1016/j.polymer.2009.09.044
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The objective of this work is to characterize and understand the structure-to-thermomechanical property relationship in thiol-ene and thiol-ene/acrylate copolymers in order to complement the existing studies on the kinetics of this polymerization reaction. Forty-one distinct three- and four-part mixtures were created with systematically varied functionality, chemical structure, type and concentration of crosslinker. The resulting polymers were subjected to dynamic mechanical analysis and tensile testing at their respective glass transition temperature, T-g, to quantify and understand their thermomechanical properties. The copolymer systems exhibited a broad range of T-g, rubbery modulus - E-r and failure strain. The addition of a difunctional high-T-g acrylate to several three-part systems increased the resultant T-g and E-r. Higher crosslink densities generally resulted in higher stress and lower strain at failure. The tunability of the thermomechanical properties of these copolymer systems is discussed in terms of inherent advantages and limitations in light of pure acrylate systems. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5549 / 5558
页数:10
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