自愈水凝胶
纤维素
离子液体
微晶纤维素
甲壳素
环氧氯丙烷
纳米纤维素
生物高聚物
化学工程
化学
高分子化学
材料科学
水溶液
壳聚糖
有机化学
聚合物
工程类
催化作用
作者
Xiaoping Shen,Julia L. Shamshina,Paula Bertón,Jenny Bandomir,Hui Wang,Gabriela Gurău,Robin D. Rogers
标识
DOI:10.1021/acssuschemeng.5b01400
摘要
Physical and/or covalently linked (chemical) hydrogels were prepared from chitin and cellulose extracted with ionic liquid from shrimp shells and wood biomass, respectively, and compared with hydrogels prepared from commercially available biopolymers, practical grade chitin, and microcrystalline cellulose. The highly porous aerogels were formed by initial dissolution of the biopolymers in NaOH/urea aqueous systems using freeze/thaw cycles, followed by thermal treatment (with or without epichlorohydrin as a cross-linker) and supercritical CO2 drying. The ionic-liquid-extracted cellulose pulp and chitin, as well as practical grade chitin could form both stable physical and chemical hydrogels, whereas biopolymers of lower apparent molecular weight such as microcrystalline cellulose required a covalent cross-linker for hydrogel formation and commercially available pure chitin was not suitable for the preparation of hydrogels of either type. Hydrogels prepared from the ionic-liquid-extracted biopolymers exhibited properties substantially different from those made from the commercially available biopolymers. Loading of an active ingredient into the hydrogel and its subsequent release was demonstrated using indigo carmine and revealed that the release rate was controlled mainly by the biopolymer concentration of the gel network.
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