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CeO_2/SiO_2的制备及丁烯异构化动力学

Preparation of CeO_2/SiO_2 and Kinetics of Isomerization of Butene
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摘要 用浸渍法制备CeO_2/SiO_2催化剂.催化剂灼烧温度在300-500℃时2-丁烯异构化活性保持一常数;600℃灼烧时活性下降,活载比在1/32-1/5范围内,随活载比增加催化剂活性呈线性增加.在2-丁烯分压较低时,t-2-丁烯及c-2-丁烯异构成1-丁烯的反应级数接近于一级.1-丁烯分压较大时1-丁烯异构成t-2-丁烯及c-2-丁烯的动力学服从于反应物、反应产物吸附的L-H动力学方程.用正交设计法估计动力学参数.1-丁烯、t-2-丁烯及c-2-丁烯吸附热的估计值与脉冲法测定值一致. Catalysts, CeO2/SiO2, were prepared by the impregnated method. The activity of the catalysts at calcination temperattire of the catalysts in the range 300-500 ℃ was constant and decreased at 600℃. The catalystic activity in the range of ratio of CeO2 to SiO2, 1/5-1/32, increased linearly. The reaction order with respect to t-2-butene or c-2-butene was first prokimate1y at low partial pressuxes of t-2-butene or c-2-butene.At higher partial pressuxes of t-2-butene or c-2-butene the kinetics of isomerization of 1-butene obeys the L-H mechanism equation with adsorption of 1-butene, t-2-butene and c-2-butene. The kinetic paraxneters were estimated by the method of orthogonal design.The estimated values of adsorption of 1-butene, t-2-butene and c-2-butene are coincided with the experimental values by the pulse method.
机构地区 北京大学化学系
出处 《物理化学学报》 SCIE CAS CSCD 北大核心 1995年第1期9-14,共6页 Acta Physico-Chimica Sinica
关键词 动力学 催化 丁烯异构化 氧化铈 氧化硅 CeO_2/SiO_2 Kinetics L-H equation
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参考文献3

  • 1俞启全,北京大学学报,1986年,6期,17页
  • 2马希文,正交设计的数学理论,1981年
  • 3Wei J,Adv Catal,1962年,13卷,203页

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