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Synthesis of Mesoporous Silica Submicrospheres with High Specific Surface Area via a Modified Octylamine Templating Process

机译:改性辛胺模板反应法合成高比表面积介孔二氧化硅亚微球

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摘要

Mesoporous silica submicrospheres with high specific surface area, 930.9m~2/g, were synthesized without using any acid or alkali as catalyst. Tetraethoxysilane as silica source, octylamine as template and polyoxyethylene (20) sorbitan monolaurate as emulsifier were adopted in this work. The as-prepared spheres were characterized with scanning electron microscopy, energy disperse spectroscopy, thermal gravimetric analysis, small angle X-ray diffraction and nitrogen adsorption, respectively. The results showed that octylamine vesicles were incorporated by silica shell in dilute sodium chloride solution, and the morphology and dispersity of submicrospheres were improved by using polyoxyethylene (20) sorbitan monolaurate. Moreover, the size of as-prepared products was gradually decreased as the amounts of polyoxyethylene (20) sorbitan monolaurate increased. In addition, the shell of the submicrospheres with narrowly distributed nanopores became more and more unordered with the prolonging of the calcinating time.
机译:不用任何酸或碱作催化剂,合成了比表面积为930.9m〜2 / g的中孔二氧化硅亚微球。本研究采用四乙氧基硅烷作为二氧化硅源,辛胺为模板,聚氧乙烯(20)脱水山梨醇单月桂酸酯为乳化剂。分别用扫描电子显微镜,能量分散谱,热重分析,小角X射线衍射和氮吸附对制得的球进行表征。结果表明,将辛胺胺囊泡通过二氧化硅壳掺入稀氯化钠溶液中,并使用聚氧乙烯(20)脱水山梨糖醇单月桂酸酯改善了亚微球的形貌和分散性。此外,随着聚氧乙烯(20)脱水山梨糖醇单月桂酸酯的量增加,所制备产品的尺寸逐渐减小。另外,随着煅烧时间的延长,具有狭窄分布的纳米孔的亚微球壳变得越来越无序。

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