Influence of soft segment composition on phase-separated microstructure of polydimethylsiloxane-based segmented polyurethane copolymers

被引:136
作者
Choi, Taeyi [1 ]
Weksler, Jadwiga [2 ]
Padsalgikar, Ajay [2 ]
Runt, James [1 ]
机构
[1] Penn State Univ, Dept Mat Sci & Engn, University Pk, PA 16802 USA
[2] AorTech Biomat, Scoresby, Vic 3179, Australia
关键词
Polyurethane; Microstructure; Small-angle X-ray scattering; ANGLE X-RAY; SCATTERING DATA; MICRODOMAIN STRUCTURE; URETHANE ELASTOMERS; MORPHOLOGY; BIOSTABILITY; IONOMERS; CONNECTIVITY; ORGANIZATION; POLYMERS;
D O I
10.1016/j.polymer.2009.03.024
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Segmented polyurethane block copolymers were synthesized using 4,4'-methylenediphenyl diisocyanate (MDI) and 1,4-butanediol (BDO) as hard segments and various soft segments derived from poly(hexamethylene oxide) (PHMO) and poly(dimethylsiloxane) (PDMS)-based macrodiols and mixtures thereof. The microstructure and degrees of phase separation were characterized using a variety of experimental methods. Copolymers synthesized with the PDMS macrodiol and from PDMS/PHMO macrodiol mixtures were found to consist of three phases: a PDMS phase: hard domains; and a mixed phase of PHMO, PDMS ether end group segments and some dissolved hard segments. Two models were used to characterize the small-angle X-ray scattering from these copolymers: pseudo two-phase and core-shell models. Analysis using both methods demonstrates that as the PDMS content in the soft segment mixture increases, the greater the fraction of hard segments involved in hard domains than are dissolved in the mixed phase. Findings from analysis of the carbonyl region of FTIR spectra are also in agreement with greater hard/soft segment demixing in copolymers containing higher PDMS contents. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2320 / 2327
页数:8
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