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Microwave-assisted rapid synthesis of poly(glycerol-sebacate) elastomers

机译:微波辅助快速合成聚癸二酸甘油酯弹性体

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摘要

Poly(glycerol-sebacate) (PGS) was introduced a decade ago as a potential material for soft tissue repair. All of the proposed copolymerization reactions in the literature include a two-stage (prepolymerization and curing) synthesis where the reaction times can take as long as several days. This study, on the other hand, proposes a new route that eliminates these disadvantages and enables a rapid synthesis of PGS elastomers via microwave-assisted prepolymerization in minutes instead of days. No purge gas, catalyst or vacuum is needed in the first prepolymerization step. The curing stage was carried out at 150℃ for 4, 8, 16, and 24 hours. The glass transition temperature (T_g) and melting temperatures for the glycerol and sebacic acid fragments (T_(m_1) and T_(m_2)) of these PGS elastomers were found as -35.61 ℃, -15.82 ℃, and 61.70 ℃, respectively. The Young's modulus and tensile strength values were found as 0.50 ± 0.02 MPa and 0.27 ± 0.06 MPa, respectively.
机译:聚癸二酸甘油酯(PGS)是十年前作为软组织修复的潜在材料而引入的。文献中所有建议的共聚反应都包括两阶段(预聚合和固化)合成,其中反应时间可能长达几天。另一方面,这项研究提出了一种新途径,该途径消除了这些缺点,并能够在数分钟而不是数天的时间内通过微波辅助预聚合快速合成PGS弹性体。在第一预聚合步骤中不需要吹扫气体,催化剂或真空。固化阶段在150℃下进行4、8、16和24小时。这些PGS弹性体的甘油和癸二酸片段的玻璃化转变温度(T_g)和熔融温度(T_(m_1)和T_(m_2))分别为-35.61℃,-15.82℃和61.70℃。杨氏模量和抗拉强度值分别为0.50±0.02 MPa和0.27±0.06 MPa。

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