高校化学工程学报
高校化學工程學報
고교화학공정학보
JOURNAL OF CHEMICAL ENGINEERING OF CHINESE UNIVERSITIES
2015年
1期
116-121
,共6页
罗忠新%高芒来%叶亚格%刘月宁%路来福
囉忠新%高芒來%葉亞格%劉月寧%路來福
라충신%고망래%협아격%류월저%로래복
酸活化%双季铵盐%膨润土%表征%酯化反应%催化
痠活化%雙季銨鹽%膨潤土%錶徵%酯化反應%催化
산활화%쌍계안염%팽윤토%표정%지화반응%최화
acid-treatment%bis-quaternary ammonium salts%bentonite%characterization%esterification%catalysis
首先以六甲基乙二铵二甲硫酸盐(EDAS)、六甲基己二铵二甲硫酸盐(HDAS)及六甲基癸二铵二甲硫酸盐(DDAS)三种不同链长双季铵盐改性膨润土,然后用HCl活化,制备酸化双季铵型有机膨润土。采用N 2吸附技术、XRD、IR、TG及SEM等分析手段表征,并以乙酸与正丁醇的酯化反应为探针,初步研究其催化性能和结构关系。结果表明,酸活化及有机改性改变了膨润土的层状硅酸盐结构,比表面积及孔体积均增加,主要是由微孔比例增加引起;双季铵盐成功进入到膨润土层间,并以单层平卧的方式排列。酸活化有机膨润土使乙酸的转化率提高了20%~30%,通过正交实验得到较优的酯化条件为:正丁醇与乙酸的摩尔比2.5,反应温度130℃,反应时间4 h,催化剂用量0.4 g。
首先以六甲基乙二銨二甲硫痠鹽(EDAS)、六甲基己二銨二甲硫痠鹽(HDAS)及六甲基癸二銨二甲硫痠鹽(DDAS)三種不同鏈長雙季銨鹽改性膨潤土,然後用HCl活化,製備痠化雙季銨型有機膨潤土。採用N 2吸附技術、XRD、IR、TG及SEM等分析手段錶徵,併以乙痠與正丁醇的酯化反應為探針,初步研究其催化性能和結構關繫。結果錶明,痠活化及有機改性改變瞭膨潤土的層狀硅痠鹽結構,比錶麵積及孔體積均增加,主要是由微孔比例增加引起;雙季銨鹽成功進入到膨潤土層間,併以單層平臥的方式排列。痠活化有機膨潤土使乙痠的轉化率提高瞭20%~30%,通過正交實驗得到較優的酯化條件為:正丁醇與乙痠的摩爾比2.5,反應溫度130℃,反應時間4 h,催化劑用量0.4 g。
수선이륙갑기을이안이갑류산염(EDAS)、륙갑기기이안이갑류산염(HDAS)급륙갑기계이안이갑류산염(DDAS)삼충불동련장쌍계안염개성팽윤토,연후용HCl활화,제비산화쌍계안형유궤팽윤토。채용N 2흡부기술、XRD、IR、TG급SEM등분석수단표정,병이을산여정정순적지화반응위탐침,초보연구기최화성능화결구관계。결과표명,산활화급유궤개성개변료팽윤토적층상규산염결구,비표면적급공체적균증가,주요시유미공비례증가인기;쌍계안염성공진입도팽윤토층간,병이단층평와적방식배렬。산활화유궤팽윤토사을산적전화솔제고료20%~30%,통과정교실험득도교우적지화조건위:정정순여을산적마이비2.5,반응온도130℃,반응시간4 h,최화제용량0.4 g。
Hexamethyl ethyl diammonium methylsulfate (EDAS), hexamethyl hexyl diammonium methylsulfate (HDAS) and hexamethyl decyl diammonium methylsulfate (DDAS) were used to modify bentonites separatively, which were then activated with HCl to obtain acid-treated organobentonites. The microstructure of the organobentonites was respectively characterized by N2 adsorption, IR, X-ray diffraction, thermogravimetric analysis and SEM, and their catalytic activity was studied through the esterification reaction of acetic acid andn-butyl alcohol. The results show that the silicate layer skeleton structure changes after organic modification and acid-treatment, and the specific surface area and pore volume of the bentonite increase, which is mainly caused by the increase of micropores. Quaternary ammonium salts readily intercalate into the bentonite interlayer and arrange in monolayer state. The conversion of acetic acid increases by 20%~30% when using acid-treated organobentonites as catalysts. Optimized conditions were obtained by orthogonal test as follows: the molar ratio ofn-butyl alcohol to acetic acid is 2.5:1.0, reaction temperature is 130℃, reaction time is 4.0 h and catalyst dosage is 0.4 g.