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Organic/inorganic Dual Network Hydrogels Based on Acrylic Acid and 2-aminoethyl-3-aminopropyltrimetoxysilane: Synthesis and Characterization

机译:基于丙烯酸和2-氨基乙基-3-氨基丙基三乙酰硅烷的有机/无机双网络水凝胶:合成和表征

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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.
机译:基于部分中和的聚丙烯酸(PAANA)和POPE-N-(2-氨基乙基1)-3-AMINOPROPOCT1TRIMETHOXYSI1A烷(PAPTMS)的一种新型双网络(DN)水凝胶复合材料通过AANA存在的自由基聚合的组合来合成N,N'-亚甲基比(丙烯酰胺)交联剂和水解二氧化硅前体和催化诱导的APTMS的羟基的羟基缩合(从5-20重量%)形成网络结构。通过FTIR分析,通过不存在C = C双键验证了Paana的交联。与纯PAA水凝胶相比,Paana / PAIP水凝胶的TGA显示出较高的热稳定性以及Paaana / PAIP复合材料的耐热指数(Tiiri)具有比添加剂更大的值。在掺入10wt%的PAPT的掺入时,水凝胶在蒸馏水中的溶胀容量增强了316%(从16.81至70.06g / g)。水凝胶的扩散机制(Paana / PAIPMS = 80/20之外)具有非Fickian或异常的性格。 paana / paptms = 80/20样品的吸附曲线具有乙状结构的特征,并作为一阶动力学和整体自催化过程的组合而被解释为其两个速率常数。

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