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A comparative study on the synthesis mechanism and microstructural development of hierarchical porous mullite monoliths obtained by the sol-gel process with three different silicon sources

机译:用三种不同硅源的溶胶 - 凝胶法得到的分层多孔莫来石体整体性促进的比较研究

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摘要

Hierarchical porous mullite monoliths have been prepared via a sol-gel process accompanied by phase separation. Propylene oxide (PO) acted as an acid scavenger to mediate the gelation, poly(ethylene oxide) (PEO) as the phase-separation inducer and network former, aluminum chloride hexahydrate (AlCl3 center dot 6H(2)O) as the aluminum source. The route was improved by using hypotoxic tetraethylorthosilicate (TEOS) and nontoxic aqueous colloidal silica (Aq) instead of tetramethoxysilane (TMOS). The synthesis mechanism and microstructural development were comparatively investigated by scanning electron microscopy (SEM), thermogravimetry-differential thermal analysis (TG-DTA), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and nitrogen adsorption-desorption. It was found that the mixing degree of precursors and concurrent process of gelation and phase separation are key elements to get well-defined hierarchical porous mullite monoliths. In addition, the monoliths with high relative crystallinity are more likely to be obtained under low transformation temperature in organic silicon sources system. (C) 2015 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
机译:已经通过相分离伴随的溶胶 - 凝胶法制备了等级多孔莫来石体。环氧丙烷(PO)用作酸化清除剂,以介导胶凝,聚(环氧乙烷)(PEO)作为相分离式诱导剂和网络以上,氯化铝六水合物(ALCL3中心点6H(2)O)作为铝源。通过使用低毒四乙氨酸硅酸盐(TEOS)和无氧基含水胶体二氧化硅(水溶液)而不是四甲氧基硅烷(TMOS)来改善该途径。通过扫描电子显微镜(SEM),热重差异差分热分析(TG-DTA),X射线衍射(XRD),傅里叶变换红外光谱(FTIR)和氮吸附 - 解吸来相对研究合成机制和微观结构显影。结果发现,凝胶化和相分离的前体和并发过程的混合程度是获得定义明确的分层多孔莫来石体整体的关键元素。另外,在有机硅源系统中的低转化温度下,更可能获得具有高相对结晶度的整料。 (c)2015 Elsevier Ltd和Techna Group S.R.L.版权所有。

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