Highly selective vapor phase Beckmann rearrangement over H-USY zeolites
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作者:
Dai, LX
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Univ Tokyo, Grad Sch Engn, Dept Appl Chem, Bunkyo Ku, Tokyo 1138656, JapanUniv Tokyo, Grad Sch Engn, Dept Appl Chem, Bunkyo Ku, Tokyo 1138656, Japan
Dai, LX
[1
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Koyama, K
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Univ Tokyo, Grad Sch Engn, Dept Appl Chem, Bunkyo Ku, Tokyo 1138656, JapanUniv Tokyo, Grad Sch Engn, Dept Appl Chem, Bunkyo Ku, Tokyo 1138656, Japan
Koyama, K
[1
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Miyamoto, M
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Univ Tokyo, Grad Sch Engn, Dept Appl Chem, Bunkyo Ku, Tokyo 1138656, JapanUniv Tokyo, Grad Sch Engn, Dept Appl Chem, Bunkyo Ku, Tokyo 1138656, Japan
Miyamoto, M
[1
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Tatsumi, T
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Univ Tokyo, Grad Sch Engn, Dept Appl Chem, Bunkyo Ku, Tokyo 1138656, JapanUniv Tokyo, Grad Sch Engn, Dept Appl Chem, Bunkyo Ku, Tokyo 1138656, Japan
Tatsumi, T
[1
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机构:
[1] Univ Tokyo, Grad Sch Engn, Dept Appl Chem, Bunkyo Ku, Tokyo 1138656, Japan
The vapor Beckmann rearrangement of cyclohexanone oxime to epsilon-caprolactam catalyzed by H-USY with different SiO2/Al2O3 ratios was studied. The catalytic performance of H-USY zeolites for the highly selective formation of epsilon-caprolactam was greatly improved by adjusting the SiO2/Al2O3 ratio and by using an appropriate diluent. It has been found that H-USY catalysts with SiO2/Al2O3 ratios of 27 and 62 exhibited excellent catalytic activity, selectivity and stability when 1-hexanol was used as diluent. The NH3-TPD results indicate that an appropriate amount of relatively weak acid sites of H-USY zeolites are effective for highly selective Beckmann rearrangement. The interaction of alcohols with H-USY zeolites has been investigated by FT-IR to explain the improving effect of 1-hexanol. (C) 1999 Elsevier Science B.V. All rights reserved.