From micro to macro: Physical-chemical characterization of wheat starch-based films modified with PEG200, sodium citrate, or citric acid

淀粉 化学工程 柠檬酸 聚合物 食品包装 材料科学 聚乙二醇 溶剂 挤压 肿胀 的 增塑剂 高分子化学 化学 有机化学 复合材料 食品科学 工程类
作者
Veronica Ciaramitaro,Elena Piacenza,Paolo Lo Meo,Calogero Librici,Martina Maria Calvino,Pellegrino Conte,Giuseppe Lazzara,Delia Chillura Martino
出处
期刊:International Journal of Biological Macromolecules [Elsevier BV]
卷期号:253: 127225-127225 被引量:2
标识
DOI:10.1016/j.ijbiomac.2023.127225
摘要

Needing to extend the shelf-life of packaged food and the evolving consumer demands led researchers to seek innovative, eco-friendly, and biocompatible packaging solutions. Starch is among the most promising natural and renewable alternatives to non-degradable plastics. Here, we deeply study the structural features of starch films modified by adding citric acid (CA) or sodium citrate (SC) as a cross-linker and polyethylene glycol 200 (PEG200) as a plasticizer and obtained through solvent casting. The substances' influence on starch films was evaluated through Attenuated Total Reflection Fourier Transform Infrared (ATR-FTIR) and Solid-state Nuclear Magnetic Resonance (ss-NMR) spectroscopies. Films' macroscopic properties, such as swelling index, solubility, thermo-mechanical features, and moisture absorption, were also assessed to foresee potential applications. Proper amounts of CA, CS, and PEG200 improve film properties and inhibit starch chains' retrogradation and recrystallization. Besides, the chemical neighbourhood of nuclei observed through ss-NMR significantly changed alongside the polymer chains' mobility. The latter result indicates a different polymer chain structural organization that could justify the film's higher resistance to thermal degradation and elongation at the break. This methodological approach is effective in predicting the macroscopic behaviour of a polymeric material and could be helpful for the application of such products in food preservation.
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