化学学报 ›› 1997, Vol. 55 ›› Issue (5): 474-479. 上一篇    下一篇

研究论文

KF负载制备固体强碱的研究

朱建华;须沁华   

  1. 南京大学化学系
  • 发布日期:1997-05-15

Investigation on the solid strong bases derived from supported KF

ZHU JIANHUA;XU QINHUA   

  • Published:1997-05-15

本文探讨了KF/Al2O3具有高碱性的原因。KF预吸附痕量H2O后具有碱性且能化学吸附CO2, 但这些部分水合状态的F^-的碱性太弱, 还不能催化丁烯异构化反应。IR和TPDE结果证实KF/Al2O3在丁烯异构化反应中的主要活性位具有[Al-OH...F^-]物种。这些强碱位可在高温脱羟而被破坏, 导致KF/Al2O3的失活。KF被首次报道负载在AlPO4-5上产生强碱位并能催化丁烯异构化反应。

关键词: 催化, 红外分光光度法, 氧化铝, 二氧化碳, 吸附, 丁烯, 氟化钾, 异构化

In the present study, the reason for the high basicity of KF/Al2O3 and the nature of the basic active sites on KF/Al2O3 were explored. KF modification has also been applied to other metal oxides and molecular sieves. Hydration could produce some partially hydrated fluoride species and promote CO2 adsorption on KF and KF/CaF2, but the basicity of these species was too weak to catalyze 1-butene isomerization at 273K. The effect of pretreatment temperature on the basicity of KF/Al2O3 was examined. Based on the results of Temperature Programmed Decomposition (TPDE), FTIR and probe reaction, the [Al-OH...F^-] species were recognized to be the main active species on KF/Al2O3 in 1-butene isomerization at 273K. Dehydroxylation at high temperature could destroy or suppress these species and caused deactivation on KF/Al2O3. KF was firstly reported to be supported on AlPO4-5 molecular sieve. Through the interaction with the support, KF modification can create strong basic sites on AlPO4-5 and catalyse the butene isomerization at 273K.

Key words: CATALYSIS, INFRARED SPECTROPHOTOMETRY, ALUMINIUM OXIDE, CARBON DIOXIDE, ADSORPTION, BUTENE, POTASSIUM FLUORIDE, ISOMERIZATION

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