硅烷化改性凹凸棒石负载磷钨钼杂多酸催化合成乙酸正戊酯  

Preparation of n-Amyl Acetate over Silylated-Attapulgite Supported 12-Heteropolyacid of Molybdenum and Tungsten Catalyst

作　　者：李贵贤[1] 穆瑞娜[1] 范宗良[1] 李亚珍[1] 

机构地区：[1]兰州理工大学石油化工学院,甘肃兰州730050

出　　处：《石油化工》2013年第2期185-190,共6页Petrochemical Technology

基　　金：国家自然科学基金项目(20961004)

摘　　要：以杂多酸H3PW6Mo6O40(PWMo)为活性组分,硅烷化改性的凹凸棒石(KH550-Pa)为载体,采用浸渍法制备了负载型PWMo/KH550-Pa催化剂,利用FTIR和XRD等方法对其结构进行了表征,并考察了其在乙酸正戊酯合成反应中的催化性能。实验结果表明,PWMo/KH550-Pa催化剂中的PWMo仍保持Keggin结构,并以离子对形式均匀、随机地分布在载体的表面及孔径内;在乙酸正戊酯的合成反应中,杂多酸PWMo适宜的负载量为30%(w);催化剂用量、反应温度、反应时间、n(乙酸)∶n(正戊醇)对乙酸正戊酯的选择性影响不大;以30%PWMo/KH550-Pa为催化剂的适宜反应条件为:催化剂用量0.1 g、正戊醇0.045 mol、n(乙酸)∶n(正戊醇)=4∶1、125℃、2.5 h,在此条件下正戊醇的转化率为92.34%,乙酸正戊酯的收率可达91.70%。A supported heteropoly acid catalyst PWMo/KH550-Pa was prepared by an impregnation method with H3PW6Mo6O40（PWMo） as the active component and silylated-attapulgite（KH550-Pa） as the support. The structure of the catalyst was characterized by means of FTIR and XRD, and its catalytic performance in the synthesis of n-amyl acetate from n-amyl alcohol and acetic acid was investigated. The results show that PWMo immobilized on KH550-Pa remains a Keggin structure with uniform and random distribution in the form of ion-pairs on the support. In the synthetic reaction, the influences of catalyst dosage, reaction temperature, reaction time and molar ratio of alcohol to acid on the selectivity to n-amyl acetate can be neglected. Under the optimized conditions of PWMo loading 30%（w）, PWMo/KH550-Pa dosage 0.1 g, n-amyl alcohol 0.045 mol, n（acetic acid） ： n（n-amyl alcohol） 4 ： 1, 125℃ and 2.5 h, conversion of n-amyl alcohol and yield of n-amyl acetate reached 92.34% and 91.70%, respectively.

关 键 词：硅烷化凹凸棒石 磷钨钼杂多酸催化剂 酯化反应 乙酸正戊酯 

分 类 号：TQ426.91[化学工程]