CIESC Journal

• 化工学报 • 上一篇    下一篇

二氧化硫在钒催化剂上氧化动力学的研究——Ⅰ.永利钒催化剂的动力学方程式

张曼徵,郭慎独,汪师俊,翁文生,陈豫   

  1. 中国科学院应用化学研究所 ,中国科学院应用化学研究所 ,中国科学院应用化学研究所 ,中国科学院应用化学研究所 ,中国科学院应用化学研究所
  • 出版日期:1957-12-25 发布日期:1957-12-25

KINETIC STUDIES ON THE OXIDATION OF SULFUR DIOXIDE ON VANADIUM CATALYST——I. Rate Equations with Yung-lee Catalyst

CHANG MAN-CHEN, Kuo SHEN-TU, WANG SHIH-CHUN, WUNG WEN-SHBN and CHEN Yu Institute of Applied Chemistry, Academia Sinica   

  • Online:1957-12-25 Published:1957-12-25

摘要: <正>二氧化硫在钒催化剂上的氧化动力学问题,已经有很多人进行过研究。不过异相催化过程一般是比较复杂的,影响催化速度的因素除了催化剂本身的化学及表面性质,反应的温度,反应物与生成物的浓度之外,还有反应物或生成物在催化剂表面上的吸附或解吸速度,到达或离开催化剂表面上的物质传递过程的速度等复杂性。

Abstract: Kinetics of the oxidation of sulfur dioxide on Vanadium catalyst used in the sulfuric acid contact process is complicated not only by diffusional processes but also by the change occurring in the catalyst itself. Kinetic studies have been carried out in flow reactors at different temperatures with catalyst granules of different sizes. The effects of mass transfer have been observed. With catalyst size as ordinarily used in industry (5 mm), the reaction rate is much retarded by diffusional processes and is controlled kinetically by outer diffusion when temperature is higher than 500℃. Different rate equations are obtained with different granular sizes of the catalyst. There exists a range of temperature in which the activity of the catalyst changes according to the operating conditions. Direct observation of the catalyst in operation shows that the catalyst is bluish-green in color at 400℃ and becomes yellowish at 500℃. At 450℃ about half of the catalyst bed from the gas inlet end is bluish-green in color and the other half toward the gas exit end yellowish. The proportion of these two colored parts changes with the operating conditions. A lower activity corresponds to more of the catalyst in bluish-green color and a higher activity to more of the catalyst in yellowish. The rate equation obtained changes in form as the catalyst changes in color (the influence of rate of mass transfer not involved). For the foreward reaction at 400℃,For the reverse reaction at 550℃, Below 475℃ the activation energy is 50 Kcal/mol, but above 475℃ it becomes 24 Kcal/mol. The reduction of activation energy is due to change of the catalyst itself but not to the effect of diffusional processes. Examination of the rate equations according to the theory of indicates that the rate determining step is the reaction in the absorbed layer.