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首页> 外文期刊>Comptes Rendus Chimie >Template-free sol-gel synthesis of high surface area mesoporous silica based catalysts for esterification of di-carboxylic acids
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Template-free sol-gel synthesis of high surface area mesoporous silica based catalysts for esterification of di-carboxylic acids

机译:无模板的溶胶-凝胶法合成高表面积介孔二氧化硅基催化剂,用于二羧酸的酯化

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High surface area mesoporous silica based catalysts have been prepared by a simple hydrolysis/sol-gel process without using any organic template and hydrothermal treatment. A controlled hydrolysis of ethyl silicate-40, an industrial bulk chemical, as a silica precursor, resulted in the formation of very high surface area (719 m(2)/g) mesoporous (pore size 67 angstrom and pore volume 1.19 cc/g) silica. The formation of mesoporous silica has been correlated with the polymeric nature of the ethyl silicate-40 silica precursor which on hydrolysis and further condensation forms long chain silica species which hinders the formation of a close condensed structure thus creating larger pores resulting in the formation of high surface mesoporous silica. Ethyl silicate-40 was used further for preparing a solid acid catalyst by supporting molybdenum oxide nanoparticles on mesoporous silica by a simple hydrolysis sol gel synthesis procedure. The catalysts showed very high acidity as determined by NH3-TPD with the presence of Lewis as well as Brensted acidity. These catalysts showed very high catalytic activity for esterification: a typical acid catalyzed organic transformation of various mono- and di-carboxylic acids with a range of alcohols. The in situ formed silicomolybdic acid heteropoly-anion species during the catalytic reactions were found to be catalytically active species for these reactions. Ethyl silicate-40, an industrial bulk silica precursor, has shown a good potential for its use as a silica precursor for the preparation of mesoporous silica based heterogeneous catalysts on a larger scale at a lower cost. (C) 2016 Published by Elsevier Masson SAS on behalf of Academie des sciences.
机译:高表面积的介孔二氧化硅基催化剂是通过简单的水解/溶胶-凝胶法制备的,无需使用任何有机模板和水热处理。硅酸乙酯-40(一种工业用大宗化学品)的受控水解,作为二氧化硅的前体,导致形成非常高的介孔表面积(719 m(2)/ g)(孔径67埃,孔容1.19 cc / g) )二氧化硅。中孔二氧化硅的形成与硅酸乙酯-40二氧化硅前体的聚合性质有关,后者在水解和进一步缩合后会形成长链二氧化硅,从而阻碍了紧密缩合结构的形成,从而形成较大的孔洞,从而形成高孔隙率的二氧化硅。表面介孔二氧化硅。通过简单的水解溶胶凝胶合成方法,通过将氧化钼纳米颗粒负载在中孔二氧化硅上,将硅酸乙酯-40进一步用于制备固体酸催化剂。如存在路易斯的情况下,由NH3-TPD测定的催化剂显示出非常高的酸度以及布朗斯台德酸度。这些催化剂显示出很高的酯化催化活性:典型的酸催化各种单羧酸和二羧酸与一系列醇的有机转化。发现在催化反应过程中原位形成的硅钼酸杂多阴离子物质是这些反应的催化活性物质。硅酸乙酯-40,一种工业本体二氧化硅前体,已显示出其用作用于以较低的成本大规模制备介孔二氧化硅基非均相催化剂的二氧化硅前体的良好潜力。 (C)2016由Elsevier Masson SAS代表科学研究院出版。

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