反应挤出辅助工艺与有机酸反应制备淀粉水凝胶

B. M. Marim, J. Mantovan, Gina Alejandra Gil-Giraldo, Jéssica F Pereira, B. Simões, F. Yamashita, S. Mali
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引用次数: 2

摘要

采用反应挤出法与柠檬酸和酒石酸两种有机交联剂反应制备木薯淀粉水凝胶。CA和TA的浓度分别为0、2.5、5.0、10.0、15.0和20.0%。水凝胶的取代度(DS)范围为0.023 ~ 0.365。傅里叶变换红外光谱结果表明,在1730 cm−1处出现了一个与酯羰基相关的新波段。x射线衍射结果表明,反应挤压导致天然淀粉的衍射峰消失,淀粉水凝胶中结晶度指数较低,为37%(天然淀粉)至8-11%。形貌分析表明,淀粉原有的颗粒状结构丢失,取而代之的是更粗糙、不规则的结构。反应挤出法得到的淀粉水凝胶的持水能力值优于天然淀粉和对照样品(未添加交联剂)。CA或TA浓度最高(20.0%)的水凝胶具有更高的DS和膨胀能力,样品的保水率分别为870%和810%。反应挤出与有机酸反应制备淀粉水凝胶是有效的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reactive Extrusion-Assisted Process to Obtain Starch Hydrogels through Reaction with Organic Acids
A totally green process based on reactive extrusion was used for the production of cassava starch hydrogels through reaction with two organic crosslinking agents, citric (CA) and tartaric (TA) acids. CA and TA were used at different concentrations (0, 2.5, 5.0, 10.0, 15.0, and 20.0%). Degree of substitution (DS) of hydrogels ranged from 0.023 to 0.365. Fourier transform infrared spectroscopy results showed a new band appearing at 1730 cm−1 associated with ester carbonyl groups. X-ray diffraction indicated that reactive extrusion resulted in the disappearance of diffraction peaks of native starch and samples with lower crystallinity indices ranging from 37% (native starch) to 8–11% in starch hydrogels. Morphology analysis showed that the original granular structure of starch was lost and replaced by a rougher and irregular structure. Water holding capacity values of starch hydrogels obtained by reactive extrusion were superior to those of native starch and the control sample (extruded without the crosslinking agents). Hydrogels obtained with the highest CA or TA concentration (20.0%) resulted in the higher DS and swelling capacities, resulting in samples with 870 and 810% of water retention, respectively. Reactive extrusion was effective in obtaining starch hydrogels by reaction with organic acids.
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