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Molecular design of polymer precursors for controlling microstructure of organic and carbon aerogels

机译:用于控制有机气凝胶和碳气凝胶微结构的聚合物前体的分子设计

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摘要

Organic and carbon aerogels were prepared by sol-gel polymerization of phenol, melamine and formal_dehyde, followed by supercritical drying and pyrolysis. The effect of the mole ratio of melamine/phenol (M/P) on microstructure of organic and carbon aerogels was investigated by N_2 adsorption, SEM and TEM. Coordination M/P could change the hydrophilicity and cross-linking density of polymer framework, thereby affecting polymer colloid nanoparticle nucleation and growth, and ultimately determine the 3_dimensional network of the gels. The bulk densities of organic and carbon aerogels have maxima at M/ P of 0.1, which are inversely proportional to volume shrinkage of gels during drying and pyrolysis. The size of the nanoparticles could be adjusted by varying M/P in the range from 10 to 22 nm. The mesopore volumes of organic and carbon aerogels are tailored in the range of 1.4-2.9 and 0.8-2.5 cm~3/g, respec_tively. The average mesopore diameter has experienced a decreasing first and increasing afterward ten_dency with the increase of M/P, and exhibit a minimum at M/P of 0.1.
机译:通过苯酚,三聚氰胺和甲醛的溶胶-凝胶聚合反应,然后进行超临界干燥和热解,可以制备有机气凝胶和碳气凝胶。通过N_2吸附,SEM和TEM研究了三聚氰胺/苯酚摩尔比(M / P)对有机气凝胶和碳气凝胶微观结构的影响。配位M / P可以改变聚合物骨架的亲水性和交联密度,从而影响聚合物胶体纳米颗粒的成核和生长,最终决定凝胶的三维网络。有机气凝胶和碳气凝胶的堆积密度在M / P为0.1时达到最大值,这与干燥和热解过程中凝胶的体积收缩率成反比。可以通过在10至22nm范围内改变M / P来调节纳米颗粒的尺寸。有机气凝胶和碳气凝胶的中孔体积分别设定在1.4-2.9和0.8-2.5 cm〜3 / g的范围内。随着M / P的增加,平均中孔直径先经历了下降,随后的趋势则增加,并且在M / P处表现出最小值为0.1。

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