Molecular Aggregation Structure of a Segmented Poly(urethane-urea) Elastomer Derived from an Amino Acid-Based Diisocyanate

被引:0
|
作者
Higaki, Yuji [1 ,2 ,3 ]
Suzuki, Ken [2 ]
Kojio, Ken [1 ,2 ,3 ]
Takahara, Atsushi [1 ,2 ,3 ]
机构
[1] Kyushu Univ, Inst Mat Chem & Engn, Nishi Ku, Nishi, Fukuoka 8190395, Japan
[2] Kyushu Univ, Grad Sch Engn, Nishi Ku, Nishi, Fukuoka 8190395, Japan
[3] Kyushu Univ, Int Inst Carbon Neutral Energy Res WPI I2CNER, Nishi Ku, Nishi, Fukuoka 8190395, Japan
关键词
Poly(urethane-urea) Elastomers; Lysine-Based Diisocyanate; Biodegradable Polymers; Molecular Aggregation Structure; MICROPHASE SEPARATED STRUCTURE; HARD SEGMENT; POLYURETHANE ELASTOMERS; BLOOD COMPATIBILITY; MORPHOLOGY; UREAS; DEFORMATION; COMPONENTS; DIAMINES; BEHAVIOR;
D O I
10.1295/koron.2014-0074
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We prepared segmented poly(urethane-urea)s (SPUUs) from a lysine-based diisocyanate (LDI) and an aliphatic polyester poly(epsilon-caprolactone) dial (PCL-diol), and 1,4-butanediamine (BDA). We also investigated the molecular aggregation structure, mechanical performance and biodegradability. Differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), Fourier transform infrared spectroscopy (FT-IR), wide-angle X-ray diffraction (WAXD) and small-angle X-ray scattering (SAXS) measurements indicated that the LDI-based hard segment (HS) shows weak segregation because of the bulky asymmetric chemical structure of the LDI. The stress-strain curve of PCL(1250)-LDI-BDA exhibits a yielding point and less mechanical strength than PCL(1250)-BDI-BDA because of the plastic deformation of the HS domains. PCL(1250)-LDI-BDA shows adequate biodegradability due to weak aggregation capacity of LDI-based components.
引用
收藏
页码:31 / 36
页数:6
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