首页 | 本学科首页   官方微博 | 高级检索  
     检索      

SO4^2-杭锦2^#土固体超强酸催化合成乙酸正丁酯
引用本文:魏景芳,郝向英,郭海福,白丽梅,照日格图.SO4^2-杭锦2^#土固体超强酸催化合成乙酸正丁酯[J].肇庆学院学报,2010,31(2):40-43.
作者姓名:魏景芳  郝向英  郭海福  白丽梅  照日格图
作者单位:1. 内蒙古师范大学,化学与环境科学学院,内蒙古,呼和浩特,010022;肇庆学院,化学化工学院,广东,肇庆,526061
2. 肇庆学院,化学化工学院,广东,肇庆,526061
3. 内蒙古师范大学,化学与环境科学学院,内蒙古,呼和浩特,010022
基金项目:国家自然科学基金资助项目,肇庆市科学技术计划基金资助项目 
摘    要:以硫酸处理杭锦2^#土制得的活性白土为载体,采用传统漫渍法制备了SO4^2-/杭锦2^#土固体超强酸,将该固体酸催化剂用于冰乙酸和正丁醇的酯化反应,考察了反应条件对酯化率的影响.结果表明:在醇、酸摩尔比为2:1.催化剂用量为0.6g,反应温度为90℃。反应时间为2h时,酯化率可达99.2%.显示出与硫酸为催化剂相当的活性。且催化剂可重复使用.

关 键 词:杭锦2^#土  固体超强酸  酯化反应

Synthesis of n-butyl Acetate Catalyzed by Solid Super Acid SO_4~(2-)/Hangjin 2~# Clay
WEI Jingfang,HAO Xiangying,GUO Haifu,BAI Limei,BAO Zhaorigetu.Synthesis of n-butyl Acetate Catalyzed by Solid Super Acid SO_4~(2-)/Hangjin 2~# Clay[J].Journal of Zhaoqing University (Bimonthly),2010,31(2):40-43.
Authors:WEI Jingfang  HAO Xiangying  GUO Haifu  BAI Limei  BAO Zhaorigetu
Institution:WEI Jingfang1,2,HAO Xiangying1,GUO Haifu2,BAI Limei1,BAO Zhaorigetu1(1.College of Chemistry , Environmental Science,Inner Mongolia Normal University,Hohhot Inner Mongolia 01002,China,2.College of Chemistry , Chemical Engineering,Zhaoqing University,Zhaoqing Guangdong 526061,China)
Abstract:SO4^2-/Hangjin 2^# clay solid superacid catalyst was prepared by impregnation method using activated clay (sulfuric acid-treated hangjin 2^# clay) as the support, n-butyl acetate was synthesized from n-butanol and acetic acid with SO4^2-/Hangjin 2^# clay as catalyst, The influences of reaction condition on the conversion of ester were investigated. The results reveal that the optimum conditions are:the mass of catalyst is 0.6g; the molar ratio of n-butanol to acetic acid is 2:1, reaction temperature is 90℃,reaetion time is 2 h. Under these conditions, the conversion of ester is 99.2%.catalytic activity of SO4^2-/Hangjin 2^# clay is almost equal to sulfuric acid and the catalyst can be used repeatedly.
Keywords:hangjin 2# clay  solid acid catalyst  esterification reaction  
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号