机构地区:[1]Key Laboratory of Bio-based Polymeric Materials Technology and Application of Zhejiang Province, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo 315201, China [2]School of Material Science and Chemical Engineering, Ningbo University, Ningbo 315211, China
出 处:《Chinese Journal of Polymer Science》2019年第11期1152-1161,共10页高分子科学(英文版)
基 金:financially supported by the National Key Research and Development Program of China (No. 2017YFB0309300);the National Natural Science Foundation of China (No. 51773218);Youth Innovation Promotion Association of CAS (No. 2018338);Ningbo Natural Science Foundation (No.2018A610109)
摘 要:Thermoplastic poly(ether-ester-urethane)s were synthesized from poly(L-lactide) diols (PLLA diols), polytetrahydrofuran diol (PTMG diols), 4,4'-dicyclohexylmethane diisocyanate (HMDI), and 1,4-butanediol (BDO) by a two-step reaction, and the morphology and property of the resultant TPU could be adjusted by varying the PLLA contents. The soft segment was composed of PLLA and PTMG diols. By controlling the percentage of PLLA in the soft segment, the glass transition temperature and mechanical properties of the polyurethanes could be regulated. Based on the FTIR spectrum, we found that two kinds of hydrogen bonding existed individually in soft matrix and hard domain. The hydrogen bonding in soft matrix was unstable, which could be destroyed during elongation. With in situ stretching WAXS and SAXS experiments, we found that the PLLA crystal was destroyed and the PLLA domain oriented along the stretch direction. Finally, we proposed a schematic model to illustrate the microstructures of these elastomers before and after stretch.Thermoplastic poly(ether-ester-urethane)s were synthesized from poly(L-lactide) diols (PLLA diols),polytetrahydrofuran diol(PTMG diols),4,4’-dicyclohexylmetlhane diisocyanate (HMDI),and 1,4-butanediol (BDO) by a two-step reaction,and the morphology and property of the resultant TPU could be adjusted by varying the PLLA contents.The soft segment was composed of PLLA and PTMG diols.By controlling the percentage of PLLA in the soft segment,the glass transition temperature and mechanical properties of the polyurethanes could be regulated.Based on the FTIR spectrum,we found that two kinds of hydrogen bonding existed individually in soft matrix and hard domain.The hydrogen bonding in soft matrix was unstable,which could be destroyed during elongation.With in situ stretching WAXS and SAXS experiments,we found that the PLLA crystal was destroyed and the PLLA domain oriented along the stretch direction.Finally,we proposed a schematic model to illustrate the microstructures of these elastomers before and after stretch.
关 键 词:Poly(L-lactide) DIOL POLYURETHANE Mechanical property Hydrogen bonding
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