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作 者:周伟正[1] 林德昌[1] 钟鹰[1] 郭娟[1] 王梯[1] 龙英才[1]
机构地区:[1]复旦大学化学系分子催化和新材料实验室,上海200433
出 处:《化学学报》2004年第8期833-838,共6页Acta Chimica Sinica
基 金:国家自然科学基金 (No.2 0 0 730 1 0 );教育部博士点基金 (No.980 2 4 61 3)资助项目
摘 要:在四氢呋喃 (THF) Na2 O SiO2 Al2 O3 H2 O体系中水热合成的THF FER沸石 ,经酸交换 /焙烧或焙烧 /酸交换处理可制得H FER 1和H FER 2两种H型沸石 .红外光谱及NH3 TPD等实验结果表明 ,两者的强酸位主要是对烯烃骨架异构化反应有贡献的Br nsted酸位 .10 73K/10h的高温水蒸汽处理会导致沸石骨架脱铝 ,但并未产生过多的末端硅羟基 .两者比较 ,H FER 1沸石的结构缺陷较少 ,Br nsted酸位较多 ,骨架更完美 .由THF FER沸石制备的H FER催化剂 ,对C5正构烯烃骨架异构化反应显示了优良的催化活性、选择性及稳定性 .THF-FER (ferrierite) zeolite was synthesized in the reactant system of tetrahydrofuran (THF)-Na 2O-SiO 2-Al 2O 3-H 2O. H-FER-1 and H-FER-2 were prepared by two means, ion-exchange/de-template (I) and de-template/ion-exchange (II). The FT-IR and NH 3-TPD investigations showed that the strong acid sites of H-FER zeolite, which are beneficial to the skeletal isomerization of olefin, were mainly the Brnsted acid sites. Aluminium would be removed from the framework when the samples were treated with saturated water vapor at 1073 K for 10 h. However, about 60% of Brnsted acid sites remained, and only minor terminal silanol groups were generated. Particularly, the framework of H-FER-1 sample was rather perfect with more Brnsted acid sites and less defects. The evaluations on the catalysis proved that H-FER zeolites exhibited interesting catalytic performance among activity, stability and selectivity in skeletal isomerization of C 5 olefin.
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