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负载型钒基催化剂上丙烷的临氧活化转化
引用本文:陈明树,翁维正.负载型钒基催化剂上丙烷的临氧活化转化[J].分子催化,2000,14(1):6-10.
作者姓名:陈明树  翁维正
作者单位:厦门大学,化学系,物理化学研究所,固体表面物理化学国家重点实验室,厦门,361005
基金项目:国家科技部攀登预选资助项目!(No.95-Yu-36),高等学校博士学科点专项科研基金资助课题
摘    要:用TPSR(程序升湿表面反应)-TR(FT)IR技术,研究临氧条件下丙烷负载型钒基催化剂上的活化和转化,并与催化剂的可不原性和表面酸性相关联,丙烷氧化脱氢生成丙烯与深度氧化生成COx的起始反应温度相同;而裂解产物C2H4和CH4的生成温度比丙烷氧化脱氢生成丙烯的高得多,可能主要源于丙烷的高温气相裂解,催化剂的表面酸性位和强的可还原性,有利于丙烷中C-H键的活化和临氧转化,降低起以攻提高丙烷转化率,

关 键 词:钒氧化物  丙烷  氧化还原  催化剂  临氧活化转化
文章编号:1000-3555(2000)01-0006-05

Propane Activation and Conversion over Supported Vanadia-Base Catalysts in the Presence of Oxygen
CHEN Ming shu,WENG Wei zheng,WAN Hui lin.Propane Activation and Conversion over Supported Vanadia-Base Catalysts in the Presence of Oxygen[J].Journal of Molecular Catalysis (China),2000,14(1):6-10.
Authors:CHEN Ming shu  WENG Wei zheng  WAN Hui lin
Abstract:Propane activation and conversion over supported vanadia base catalysts in the presence of oxygen were studied by Temperature Programmed Surface Reaction Time resolved Infrared Spectroscopy (TPSR TRIR). Oxidative dehydrogenation of propane to propene and deep oxidation of propane to CO x appeared to take place at the same temperature, while products C 2H 4 and CH 4 may be produced mainly from gas phase cracking of propane at high temperature. Strong reducibility and surface acidity are favorable to activate the second C-H bond in propane molecule, and result in the lowering of ignition temperature of propane oxidative dehydrogenation and increasing of the propane conversion. The adsorption of propene on acid sites leads to its total oxidation.
Keywords:Vanadia  Propane  TPSR  TRIR  Redox property  Acidity
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