首页> 外文期刊>Monatshefte fur Chemie >Optimization of catalytic activity of sulfated titania for efficient synthesis of isoamyl acetate by response surface methodology
【24h】

Optimization of catalytic activity of sulfated titania for efficient synthesis of isoamyl acetate by response surface methodology

机译:响应面法优化硫酸钛高效合成乙酸异戊酯的催化活性。

获取原文
获取原文并翻译 | 示例
           

摘要

TiO2 nanoparticles were synthesized by sol-gel method using titanium tetraisopropoxide. Sulfate ions were introduced on the titania by impregnation method using sulfuric acid as precursor of sulfate ions. Fourier transform infrared and energy-dispersive X-ray spectroscopy, X-ray fluorescence as well as X-ray diffraction, scanning electron microscopy, and BET methods were used for the characterization of the obtained nanoparticles. The esterification of isoamyl alcohol with acetic acid was investigated to prove the catalytic activity of the TiO2 nanoparticles under solvent-free conditions. Response surface methodology was applied to optimize the effect of some parameters such as the molar ratio of acetic acid to alcohol, catalyst loading, reaction temperature, and reaction time on the yield of the isoamyl acetate. The TiO2 nanoparticles were proved to be an excellent heterogeneous catalyst for isoamyl acetate synthesis under solvent-free conditions affording a high yield of 94 % under the following optimal conditions: molar ratio of acetic acid to alcohol (1:7), catalyst loading (3.2 wt% with respect to the acetic acid), the reaction temperature (130 A degrees C), and the reaction time (300 min).
机译:使用四异丙醇钛通过溶胶-凝胶法合成了TiO2纳米粒子。使用硫酸作为硫酸根离子的前体,通过浸渍法将硫酸根离子引入二氧化钛。傅里叶变换红外和能量色散X射线光谱,X射线荧光以及X射线衍射,扫描电子显微镜和BET方法用于表征所获得的纳米粒子。研究了异戊醇与乙酸的酯化反应,以证明TiO2纳米粒子在无溶剂条件下的催化活性。应用响应表面方法来优化某些参数的影响,例如乙酸与醇的摩尔比,催化剂负载,反应温度和反应时间对乙酸异戊酯收率的影响。 TiO2纳米颗粒被证明是在无溶剂条件下合成乙酸异戊酯的出色多相催化剂,在以下最佳条件下可获得94%的高收率:乙酸与醇的摩尔比(1:7),催化剂负载量(3.2)相对于乙酸的重量%),反应温度(130℃)和反应时间(300分钟)。

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