广州化工
廣州化工
엄주화공
GUANGZHOU CHEMICAL INDUSTRY AND TECHNOLOGY
2014年
18期
116-118
,共3页
胡春燕%肖伟%余丽萍%熊友发
鬍春燕%肖偉%餘麗萍%熊友髮
호춘연%초위%여려평%웅우발
固体超强酸%乙酸异戊酯%酯化%催化剂
固體超彊痠%乙痠異戊酯%酯化%催化劑
고체초강산%을산이무지%지화%최화제
rare earth solid superacid%isoamyl acetate%esterification%catalyst
以乙酸、异戊醇为原料,固体超强酸Gd3+-SO2-4/ZrO2为催化剂,催化合成乙酸异戊酯。确定了固体超强酸的最佳焙烧温度,进行了固体超强酸Gd3+-SO2-4/ZrO2和SO2-4/ZrO2催化活性对比实验,以及考察了原料酸醇比、反应时间、催化剂用量对酯化率的影响。实验结果表明:反应温度110~115℃,催化剂用量2 g, n(异戊醇):n(乙酸)=2.0:1.0,反应时间2 h,酯化率可达88.4%,催化剂重复使用效果明显,加Gd3+的固体超强酸的催化活性明显增强。
以乙痠、異戊醇為原料,固體超彊痠Gd3+-SO2-4/ZrO2為催化劑,催化閤成乙痠異戊酯。確定瞭固體超彊痠的最佳焙燒溫度,進行瞭固體超彊痠Gd3+-SO2-4/ZrO2和SO2-4/ZrO2催化活性對比實驗,以及攷察瞭原料痠醇比、反應時間、催化劑用量對酯化率的影響。實驗結果錶明:反應溫度110~115℃,催化劑用量2 g, n(異戊醇):n(乙痠)=2.0:1.0,反應時間2 h,酯化率可達88.4%,催化劑重複使用效果明顯,加Gd3+的固體超彊痠的催化活性明顯增彊。
이을산、이무순위원료,고체초강산Gd3+-SO2-4/ZrO2위최화제,최화합성을산이무지。학정료고체초강산적최가배소온도,진행료고체초강산Gd3+-SO2-4/ZrO2화SO2-4/ZrO2최화활성대비실험,이급고찰료원료산순비、반응시간、최화제용량대지화솔적영향。실험결과표명:반응온도110~115℃,최화제용량2 g, n(이무순):n(을산)=2.0:1.0,반응시간2 h,지화솔가체88.4%,최화제중복사용효과명현,가Gd3+적고체초강산적최화활성명현증강。
Isoamyl acetate was obtained by the reaction of acetic acid with isoamyl alcohol , with rare earth solid superacid Gd 3+-SO2-4 /ZrO2 as the reactive catalyst was described.The esterification reaction was performed to confirm the optimal conditions of preparation.The experiments were compared with the rare earth solid superacid Gd 3+-SO2 -4 /ZrO2 catalyst, and the ratio of isoamyl alcohol was investigated with acetic acid , reacted time, the mass of catalyst influences on the catalytic activity.The results showed that isoamyl alcohol acetate was prepared by reaction at 110 ~115 ℃for 2 h with n(isoamyl alcohol):n(acetic acid)=2.0:1.0, and(catalyst)=2 g, the conversion of acetic acid amounts was 88.4%, catalyst was used repeatedly but still had high catalytic activity , and catalytic activity of the solid super acid which added Gd 3+improved apparently.