...
首页> 外文期刊>Journal of Sol-Gel Science and Technology >Vanadia-Silica Catalysts Prepared by Sol-Gel Method:Application for Epoxidation Reaction
【24h】

Vanadia-Silica Catalysts Prepared by Sol-Gel Method:Application for Epoxidation Reaction

机译:溶胶-凝胶法制备的钒硅催化剂:在环氧化反应中的应用

获取原文
获取原文并翻译 | 示例

摘要

Vanadia-silica xerogel and aerogel catalysts,with various V/Si molar ratios (0.05,0.1,and 0.2),were prepared by sol-gel processing.Gels were obtained under acid catalysed conditions (HNO_3) from vanadium (III) acetylacetonate (V(acac)3) and tetraethoxysilane (TEOS).Under these conditions,it was found that the gelation time increased with V/Si molar ratio.The structure and catalytic properties of the mixed oxides were found to be mainly influenced by the V/Si molar ratio and drying mode.The catalytic behaviour of the xerogels and aerogels was tested in the epoxidation reaction of trans-2-hexen-l-ol.The results showed that the V/Si molar ratio did not significantly influence the catalytic activity,although the effect of drying (xerogel vs.aerogel) was remarkable.Using a molar ratio TBHP/alcohol = 4/7,the epoxide yield was about 50% in the presence of xerogels,with ca.8 h required to achieve stationary-conversion conditions in this heterogeneous-catalysis system.In contrast,the aerogel catalysts required only 2 h to reach stationary conversion conditions,due to partial leaching of the vanadium species from the solid and the associated contribution of a relatively rapid homogeneous catalysis mechanism to the overall conversion.These differences in catalytic behaviour were related to the vanadium speciation and the texture of the catalysts.To explore the origin of these differences,the catalysts were characterised by nitrogen physisorption,XPS,Raman spectroscopy,TGA/DTA and XRD.
机译:通过溶胶-凝胶法制备了具有不同V / Si摩尔比(0.05、0.1和0.2)的Vanadia二氧化硅干凝胶和气凝胶催化剂。在酸催化条件下(HNO_3)由乙酰丙酮钒(III)制备凝胶(acac)3)和四乙氧基硅烷(TEOS)。在这些条件下,发现凝胶化时间随V / Si摩尔比而增加。发现混合氧化物的结构和催化性能主要受V / Si影响在反式-2-己烯-1-醇的环氧化反应中测试了干凝胶和气凝胶的催化行为。结果表明,V / Si摩尔比对催化活性没有明显的影响,尽管使用TBHP /酒精摩尔比= 4/7,在存在干凝胶的情况下,环氧化物的收率约为50%,要达到固定转化条件,其干燥时间约为8小时。在这种非均相催化体系中。催化剂仅需2小时即可达到稳定的转化条件,这是由于钒从固体中部分浸出以及相对快速的均相催化机制对总体转化的贡献。这些催化行为的差异与钒的形态和为了探索这些差异的根源,通过氮物理吸附,XPS,拉曼光谱,TGA / DTA和XRD对催化剂进行了表征。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号