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Compositional effects on mechanical properties of nanocomposite hydrogels composed of poly(N,N-dimethylacrylamide) and clay

机译:组成对聚(N,N-二甲基丙烯酰胺)和粘土组成的纳米复合水凝胶力学性能的影响

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Nanocomposite type hydrogels (DMAA-NC gels) consisting of organic (polymer)/inorganic (clay) networks were prepared by in-situ free-radical polymerization of N,N-dimethylacrylamide (DMAA) in the presence of inorganic clay in aqueous solution. The composition of the NC gels could be controlled directly by altering the composition of the initial reaction mixture. The resulting DMAA-NC gels were mostly uniform and transparent, irrespective of their clay and polymer contents. From DSC, X-ray, TEM, and tensile mechanical measurements, the network structure was established. Contrary to conventional chemically cross-linked hydrogels (DMAA-OR gels) prepared by chemical cross-linking with a difunctional monomer, DMAA-NC gels exhibit superb mechanical properties with astonishingly large elongations at break, near to or greater than 1500%. The effects of the composition, such as the amounts of clay, polymer, and water content in DMAA-NC gels, on the tensile mechanical properties were investigated in detail. With increasing clay content from C-clay = 1 to 7 (C-clay is proportional to the weight of clay per unit volume of water, and a value of 1 corresponds to 0.762 g clay per 100 mL of water), the modulus and the ultimate tensile strength increased almost proportionally to the clay content, but the elongation at break decreased slightly. By altering the polymer content over 2 orders of magnitude, it was observed that the nature of the mechanical properties of DMAA-NC gels changed markedly. Above a lower critical polymer content (C-p approximate to 0.13), the elongation at break increased rapidly from near zero to more than 1000%. Thereafter, the hydrogels became very tough NC gels. With further increases in polymer content, the strength and the elongation at break showed maxima at certain polymer contents, whereas the modulus increased monotonically. The mechanical properties were also changed by altering the water content. The cross-link density was estimated for DMAA-NC gels with different clay contents. The effects of clay and polymer contents on the mechanical properties, as described above, were discussed on the basis of the network structure model for NC gel. [References: 36]
机译:在有机粘土的存在下,通过N,N-二甲基丙烯酰胺(DMAA)的自由基聚合,制备了由有机(聚合物)/无机(粘土)网络组成的纳米复合型水凝胶(DMAA-NC凝胶)。可以通过改变初始反应混合物的组成直接控制NC凝胶的组成。所得的DMAA-NC凝胶无论粘土和聚合物的含量如何,都基本均匀且透明。通过DSC,X射线,TEM和拉伸机械测量,确定了网络结构。与通过与双官能单体化学交联制备的常规化学交联水凝胶(DMAA-OR凝胶)相反,DMAA-NC凝胶表现出极好的机械性能,其断裂伸长率惊人地大,接近或大于1500%。详细研究了组成(如DMAA-NC凝胶中粘土,聚合物的含量和水含量)对拉伸机械性能的影响。随着粘土含量从C粘土= 1增加到7(C粘土与每单位体积的水的粘土重量成比例,值为1表示每100 mL水0.762 g粘土),模量和极限抗拉强度几乎与粘土含量成正比,但断裂伸长率略有下降。通过改变聚合物含量超过2个数量级,可以观察到DMAA-NC凝胶的机械性质的性质发生了显着变化。高于较低的临界聚合物含量(C-p约为0.13),断裂伸长率从接近零迅速增加到超过1000%。此后,水凝胶变成非常坚韧的NC凝胶。随着聚合物含量的进一步增加,强度和断裂伸长率在某些聚合物含量下显示出最大值,而模量单调增加。力学性能也通过改变水含量而改变。对于具有不同粘土含量的DMAA-NC凝胶,估计了交联密度。如上所述,在NC凝胶的网络结构模型的基础上,讨论了粘土和聚合物含量对机械性能的影响。 [参考:36]

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