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Modeling water partition in composite gels of BSA with gelatin following high pressure treatment

机译:高压处理后的BSA与明胶复合凝胶中水分配的模型

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Changes in the structural properties of hydrogels made with gelatin and bovine serum albumin mixtures were recorded following exposure to high pressure at 300 MPa for 15 min at 10 and 80 degrees C. Dynamic oscillation, SEM, FTIR and blending law modelling were utilised to rationalise results. Pressurization at the low temperature end yielded continuous gelatin networks supporting discontinuous BSA inclusions, whereas an inverted dispersion was formed at the high temperature end with the continuous BSA network suspending the discontinuous gelatin inclusions. Lewis and Nielsen equations followed the mechanical properties of the composites thus arguing that solvent partition between the two phases was always in favour of the polymer forming the continuous network. As far as we are aware, this is the first attempt to elucidate the solvent partition in pressurised hydrogel composites using blending law theory. Outcomes were contrasted with earlier work where binary mixtures were subjected only to thermal treatment.
机译:在10和80℃下于300 MPa的高压下暴露15分钟后,记录由明胶和牛血清白蛋白混合物制成的水凝胶的结构特性变化。利用动态振荡,SEM,FTIR和混合定律模型使结果合理化。在低温端加压产生了支持不连续BSA夹杂物的连续明胶网络,而在高温端形成了反向分散液,其中连续BSA网络悬浮了不连续的明胶夹杂物。 Lewis和Nielsen方程遵循复合材料的机械性能,因此认为两相之间的溶剂分配始终有利于形成连续网络的聚合物。据我们所知,这是使用混合定律理论阐明加压水凝胶复合材料中溶剂分配的首次尝试。结果与早期工作相反,早期工作仅对二元混合物进行热处理。

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