明胶
复合数
材料科学
极限抗拉强度
挤压
傅里叶变换红外光谱
组织谷氨酰胺转胺酶
化学工程
生物高聚物
化学
凝聚
吸水率
溶解度
共价键
复合材料
蜂蜡
增塑剂
高分子化学
聚合物
有机化学
酶
蜡
工程类
作者
Hui Zheng,Meiyan Zhao,Qingfeng Dong,Min Fan,Li Wang,Li Li
标识
DOI:10.1016/j.foodhyd.2022.107849
摘要
Fish gelatin (FG) is a natural biodegradable biopolymer. However, solution casting, which is commonly used to prepare gelatin films, limits large-scale film production. In this study, melt extrusion (ME) commonly used in traditional plastics was successfully applied to the preparation of gelatin composite films. The non-covalent crosslinking between hydrophobic beeswax (BW) and hydrophilic FG not only reduced the film stickiness during rolling but also decreased the water solubility of the film by 45.17% (p < 0.05). Transglutaminase (TGase) promoted covalent crosslinking between the FG networks, thereby improving the properties of the film. The results of Fourier transform infrared (FTIR) spectroscopy confirmed the crosslinking effect of BW and TGase on the gelatin films, and appropriate crosslinking maintained the forward movement of gelatin in the rotating screw according to a linear mode. The FG–BW–1%TGase film exhibited the lowest water solubility of 36.63% and the highest tensile strength of 6.26 MPa. The co-crosslinking of TGase and BW contributed to the preparation of melt-extruded composite films exhibiting desirable properties and were potential candidates for commercial food packaging.
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