丙烯酸- 2-氨基乙基-3-氨基丙基三甲氧基硅烷有机/无机双网络水凝胶的合成与表征

O. Slisenko, I. Bei, V. Budzinska, O. Tolstov
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引用次数: 0

摘要

摘要以部分中和型聚丙烯酸(PAANa)和聚N-(2-氨基乙基1)-3-氨基丙基三甲氧基硅烷(PAPTMS)为原料,在N,N ' -亚甲基双(丙烯酰胺)交联剂存在下,通过自由基聚合,水解二氧化硅前驱体,催化缩聚APTMS的羟基(5% ~ 20wt .%)形成网络结构,合成了一种新型双网络(DN)水凝胶复合材料。FTIR分析证实PAANa的交联不存在C=C双键。与纯PAA水凝胶相比,PAANa/PAPTMS水凝胶的TGA表现出更高的热稳定性,PAANa/PAPTMS复合材料的耐热指数(TiiRi)高于添加剂。当加入10%的PAPTMS时,水凝胶在蒸馏水中的溶胀能力提高了316%(从16.81 g/g提高到70.06 g/g)。除PAANa/PAPTMS = 80/20外,水凝胶的扩散机制具有非菲克式或异常性。PAANa/PAPTMS = 80/20样品的吸附曲线具有s型特征,可以解释为一级动力学和具有两个速率常数的整体自催化过程的综合结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Organic/inorganic Dual Network Hydrogels Based on Acrylic Acid and 2-aminoethyl-3-aminopropyltrimetoxysilane: Synthesis and Characterization
A novel dual network (DN) hydrogel composites based on partially neutralized polyacrylic acid (PAANa) and poly-N-(2-aminoethy1)-3-aminopropy1trimethoxysi1ane (PAPTMS) were synthesized by a combination of free radical polymerization of AANa in the presence of N,N’-methylenebis(acrylamide) cross-linker and hydrolysis of silica precursors and catalytically-induced condensation of the resulting hydroxyl groups of APTMS (from 5 to 20 wt.%) to form a network structure. The cross-linking of PAANa was verified by the absence of a C=C double bond by FTIR analysis. TGA of PAANa/PAPTMS hydrogels showed higher thermal stability compared to pure PAA hydrogel as well as the heat-resistance index (TiiRi) for PAANa/PAPTMS composites have greater values than additive ones. The hydrogels’ swelling capacity in distilled water is enhanced by 316% (from 16.81 to 70.06 g/g) at the incorporation of 10 wt% of PAPTMS. The mechanism of diffusion of hydrogels (except PAANa/PAPTMS = 80/20) has non-Fickian or anomalous character. The sorption curve of PAANa/PAPTMS = 80/20 sample has sigmoid character and was interpreted as a result of a combination of first-order kinetics and the overall autocatalytic process with its two rate constants.
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