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Ureidosilanes on E-glass fibres: deposition and surface characteristics

机译:电子玻璃纤维上的脲基硅烷:沉积和表面特性

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摘要

The behaviour of methoxy- and ethoxy-ureidosilanes deposited onto E-glass fibres from both organic and aqueous solutions is reviewed. #gamma#-Ureidopropylti(m)ethoxysilanes are used as coupling agents for paints to metal surfaces, but they have not fund much use as coupling agents for E-glass fibres. On metal surfaces, the silane is deposited with the ureido-functional group outermost, available for reaction with a paint/polymer matrix. On E-glass surfaces, however, unless specific conditions are employed, ureidosilanes tend to deposit with a highly cross-linked siloxane surface. The silanol groups condense not only with silanols of adjacent silanes and the E-glass surface, but also with aluminium hydroxides leached from the E-glass surface. This forms a highly cross-linked aluminosiloxane outer layer. The aluminosiloxane forms at all pHs between 4 and 10, and also when a range of organic deposition solvents is used. ~(29)Si-NMR results are presented which illustrate the high level of condensation; silane to silicate binding via the amino group was not detected. A small proportion of Si-O-Si (silane-glass) bonds was inferred, indicating tat a small number of sparsely distributed Si-O-Si links bound the silane to the surface. Electrokinetic analysis of the surfaces confirmed patchy deposition with a siloxane outer surface. Using AFM and ab initio calculations, it was estimated that the patchwise deposition of the silane was in the form of bilayers (or multiples of bilayers). The bilayer structure consisted of siloxane outer layers, with the inner ureido layers forming hydrogen bonds. A graphical fit using the mole and volume fractions of silane and organic solvents confirmed the various types of siloxane surfaces as deposited from different organic solvents. Chlorinated solvents tended to produce a ureido outer surface, which was condensed, but solvent-swollen; deposition from alcohol and acetone resulted in a siloxane surface. Toluene and THF both produced minimally condensed ureido surfaces, which were easily removed by washing with methylene chloride.
机译:审查了从有机溶液和水溶液中沉积到电子玻璃纤维上的甲氧基和乙氧基脲基硅烷的行为。 #γ#-Ureidopropylti(m)乙氧基硅烷被用作涂料在金属表面的偶联剂,但它们在电子玻璃纤维的偶联剂中的应用并不多。在金属表面上,硅烷沉积在最外层,具有脲基官能团,可与油漆/聚合物基体反应。然而,在电子玻璃表面上,除非采用特定条件,否则脲基硅烷倾向于在高度交联的硅氧烷表面上沉积。硅烷醇基不仅与相邻硅烷的硅烷醇和电子玻璃表面缩合,而且还与从电子玻璃表面浸出的氢氧化铝缩合。这形成了高度交联的铝硅氧烷外层。铝硅氧烷会在4至10的所有pH值下形成,并且还会使用一系列有机沉积溶剂。给出了〜(29)Si-NMR结果,表明了高的缩合度;未检测到硅烷通过氨基与硅酸盐结合。推断出一小部分的Si-O-Si(硅烷-玻璃)键,表明少量的稀疏分布的Si-O-Si键将硅烷结合到表面上。表面的电动分析证实了硅氧烷外表面的斑片状沉积。使用AFM和从头算计算,估计硅烷的分批沉积是双层(或双层的倍数)的形式。双层结构由硅氧烷外层组成,内部脲基层形成氢键。使用硅烷和有机溶剂的摩尔分数和体积分数的图形拟合证实了从不同有机溶剂沉积的各种类型的硅氧烷表面。氯化溶剂趋于产生脲基外表面,该表面凝结但溶剂溶胀。乙醇和丙酮的沉淀形成了硅氧烷表面。甲苯和THF都产生最少缩合的脲基表面,可通过用二氯甲烷洗涤轻松除去。

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