结晶度
热重分析
聚氨酯
生物相容性
六亚甲基二异氰酸酯
热稳定性
材料科学
傅里叶变换红外光谱
端羟基聚丁二烯
高分子化学
聚丁二烯
聚合
聚合物
化学工程
核化学
化学
共聚物
复合材料
工程类
冶金
作者
Kashif Zafar,Khalid Mahmood Zia,Rami M. Alzhrani,Atiah H. Almalki,Sameer Alshehri
出处
期刊:Polymers
[MDPI AG]
日期:2022-05-20
卷期号:14 (10): 2091-2091
被引量:16
标识
DOI:10.3390/polym14102091
摘要
Many investigators have focused on the development of biocompatible polyurethanes by chemical reaction of functional groups contained in a spacer and introduced in the PU backbone or by a grafting method on graft polymerization of functional groups. In this study, alginate-based polyurethane (PU) composites were synthesized via step-growth polymerization by the reaction of hydroxyl-terminated polybutadiene (HTPB) and hexamethylene diisocyanate (HMDI). The polymer chains were further extended with blends of 1,4-butanediol (1,4-BDO) and alginate (ALG) with different mole ratios. The structures of the prepared PU samples were elucidated with FTIR and 1H NMR spectroscopy. The crystallinity of the prepared samples was evaluated with the help of X-ray diffraction (XRD). The XRD results reveal that the crystallinity of the PU samples increases when the concentration of alginate increases. Thermogravimetric (TGA) results show that samples containing a higher amount of alginate possess higher thermal stability. ALG-based PU composite samples show more biocompatibility and less hemolytic activity. Mechanical properties, contact angle, and water absorption (%) were also greatly affected.
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