溶剂辅助原位分散纳米二氧化硅/聚酯生物弹性体复合材料的制备、结构及性能

Preparation, structure and properties of nano-silica/poly bioelastomer composites by solvent assistant in-situ dispersion technique

  • 摘要: 采用溶剂辅助原位分散方法, 制备纳米二氧化硅(nano-SiO2)/聚(癸二酸-甘油-柠檬酸)酯(PGSC)生物弹性体复合材料。通过FTIR、 SEM、 广角X射线衍射(WXRD)、 DSC以及力学测试等手段, 对复合材料的结构和性能进行了表征。PGSC基体不仅对nano-SiO2产生包覆, 还与nano-SiO2之间形成化学结合。随nano-SiO2质量分数增加, 其在基体中的分散更精细均匀。nano-SiO2的加入消弱了基体的有序结构, 但是无机填料网络的形成则使复合材料的有序结构增强; 加入少量nano-SiO2有利于提高基体的玻璃化转变温度(Tg), 但加入较多nano-SiO2时, Tg反而降低。复合材料具有优良的回弹性, 其拉伸强度和模量随nano-SiO2质量分数的增加而提高; 当质量分数为16.67%时, 强度和模量分别提高了602.20%和258.21%。

     

    Abstract: Nano-SiO2/poly (glycerol-sebacate-citrate)(PGSC) bioelastomer composites were prepared by solvent assistant in-situ dispersion technique, and their structure and properties were characterized by FTIR, SEM, WXRD, DSC and tensile tests. Results demonstrate that nano-SiO2 is imbedded in the PGSC matrixes, and chemical bonding is formed between them. Nano-SiO2 presents finer and more homogeneous dispersion with the increasing of its mass fractions. The ordered structures of the matrixes are weakened after nano-SiO2 is added, but the ordered structures of the composites are intensified with the formation of inorganic filler networks. The glass transition temperature (Tg) of the matrix increases when the nano-SiO2 mass fraction is lower, while the Tg decreases when its mass fraction is higher. The composites possess excellent resilience, and their tensile strength and modulus rise with the increasing of nano-SiO2 mass fractions, separately rising by 602.20% and 258.21% at its mass fraction of 16.67% than those of the pure matrixes.

     

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