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Synthesis and properties of highly hydrophilic polyurethane based on diisocyanate with ether group

机译:基于二醚异氰酸酯和醚基团的高亲水性聚氨酯的合成与性能

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摘要

Highly hydrophilic polyurethane elastomers (PUEs) were synthesized from 1,2-bis(isocyanate) ethoxyethane (TEGDI), poly(ethylene oxide-co-propylene oxide) copolyol (EOPO) and 1,4-butane diol/1,1,1-trimethylol propane (75/25) (wt/wt) by a prepolymer method. 4,4′-Diphenylmethane diisocyanate (MDI)-based PUEs were synthesized as a control as well. Fourier transform infrared spectroscopy (FT-IR) and differential scanning calorimetry (DSC) measurements revealed that the degree of microphase separation of the TEGDI-based PUEs was much weaker than for the MDI-based PUEs. Young's modulus and elongation at break of the TEGDI-based PUEs were quite lower and larger than for the MDI-based PUEs, respectively. This is due to quite weak cohesion force of the hard segment chains in the TEGDI-based PUEs. The degree of swelling of the TEGDI-based PUEs was five times larger than for the MDI-based one. This is associated with the hydrophilic nature of TEGDI and weak cohesion force in the TEGDI-based PUEs.
机译:高亲水性聚氨酯弹性体(PUE)由1,2-双(异氰酸酯)乙氧基乙烷(TEGDI),聚环氧乙烷-环氧丙烷共聚多元醇(EOPO)和1,4-丁二醇/ 1,1,1合成通过预聚物方法得到-三羟甲基丙烷(75/25)(wt / wt)。还合成了基于4,4'-二苯甲烷二异氰酸酯(MDI)的PUE。傅里叶变换红外光谱(FT-IR)和差示扫描量热法(DSC)测量表明,基于TEGDI的PUE的微相分离程度比基于MDI的PUE的弱得多。与基于MDI的PUE相比,基于TEGDI的PUE的杨氏模量和断裂伸长率分别低得多和大。这是由于基于TEGDI的PUE中硬链段的内聚力非常弱。基于TEGDI的PUE的膨胀程度是基于MDI的PUE的膨胀程度的五倍。这与TEGDI的亲水性和基于TEGDI的PUE中的弱内聚力有关。

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