首页> 外文期刊>Journal of Catalysis >FTIR and reaction studies of the acylation of anisole with acetic anhydride over supported HPA catalysts
【24h】

FTIR and reaction studies of the acylation of anisole with acetic anhydride over supported HPA catalysts

机译:负载型HPA催化剂的FTIR和苯甲醚与乙酸酐的酰化反应研究

获取原文
获取原文并翻译 | 示例
       

摘要

The behaviours of two heteropoly acid (HPA) catalysts, one supported on a commercial silica and the other on a silica-zirconia mixed oxide, were compared in the acylation of anisole with acetic anhydride. Both supported catalysts and the latter support, but not the silica, were active for the reaction, although all underwent a deactivation process before achieving complete conversion of anisole to methoxyacetophenone. The greatest yield to p-methoxyacetophenone was obtained for HPA/SiO2 while the extent of deactivation was in the order HPA/SiO2-ZrO2 > SiO2-ZrO2 > HPA/SiO2. Although acetate species accumulated on the SiO2-ZrO2 and HPA/SiO2-ZrO2 catalysts during the reaction, these species are not thought to play a role in the deactivation process. The relative extent of deactivation was consistent with the calculated ratios of adsorption coefficients which determine the strength of adsorption of product to that of anisole and indicate that product inhibition is greatest in the case of HPA/SiO2-ZrO2. Calculated absorption coefficients for pyridine adsorbed on the samples failed to distinguish between the nature of the HPA species dispersed on the two different supports. (C) 2004 Elsevier Inc. All rights reserved.
机译:比较了两种杂多酸(HPA)催化剂的行为,一种负载在市售二氧化硅上,另一种负载在二氧化硅-氧化锆混合氧化物上,将苯甲醚与乙酸酐酰化。负载的催化剂和后者的载体均对反应具有活性,尽管在实现苯甲醚完全转化为甲氧基苯乙酮之前都经历了失活过程,但二氧化硅对反应均没有活性。对于HPA / SiO2,获得最大的对甲氧基苯乙酮产率,而失活程度为HPA / SiO2-ZrO2> SiO2-ZrO2> HPA / SiO2。尽管在反应过程中乙酸盐物质在SiO2-ZrO2和HPA / SiO2-ZrO2催化剂上积累,但这些物质在失活过程中不起作用。失活的相对程度与计算出的吸附系数之比一致,后者决定了产物对苯甲醚的吸收强度,表明在HPA / SiO2-ZrO2的情况下,产物的抑制作用最大。计算出的样品中吡啶吸附的吸收系数无法区分分散在两种不同载体上的HPA种类的性质。 (C)2004 Elsevier Inc.保留所有权利。

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