CIESC Journal

• Original Article • 上一篇    下一篇

KINETICS ON EPOXIDATION OF PROPYLENE WITH ETHYLBENZENE HYDROPEROXIDE

陆乃宸; 李光福; 陆云质; 赵绪检   

  1. Institute of Chemistry, Shandong
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:1982-12-28 发布日期:1982-12-28
  • 通讯作者: 陆乃宸

KINETICS ON EPOXIDATION OF PROPYLENE WITH ETHYLBENZENE HYDROPEROXIDE

LU Naichen; LI Guangfu; LU Yunzhi; ZHAO Xujian   

  1. Institute of Chemistry, Shandong
  • Received:1900-01-01 Revised:1900-01-01 Online:1982-12-28 Published:1982-12-28
  • Contact: LU Naichen

摘要: In the range of 76°to 1200C,Dalin and others studied the kinetics on molybdenum-catalyzed epoxi-dation of propylene with ethylbenzene hydroperoxide,proposed a mechanism model of this reaction andsuggested that effective concentration of catalyst is constant during the process of epoxidation.In thispaper the reaction has been studied experimentally based on Dalin’s investigation.After analyzing thedata obtained in our experiment and those of Dalin,it is shown that the effective concentration of thecatalyst is not a constant but a variable,and its rate of consumption behaves in accordance with the firstorder reaction.Thus,the authors have modified the mechanism model in literature [3] and pointed outthat the deactivation mechanism of the catalyst is different from the inhibition mechanism described byFarberof.

Abstract: In the range of 76°to 1200C,Dalin and others studied the kinetics on molybdenum-catalyzed epoxi-dation of propylene with ethylbenzene hydroperoxide,proposed a mechanism model of this reaction andsuggested that effective concentration of catalyst is constant during the process of epoxidation.In thispaper the reaction has been studied experimentally based on Dalin’s investigation.After analyzing thedata obtained in our experiment and those of Dalin,it is shown that the effective concentration of thecatalyst is not a constant but a variable,and its rate of consumption behaves in accordance with the firstorder reaction.Thus,the authors have modified the mechanism model in literature [3] and pointed outthat the deactivation mechanism of the catalyst is different from the inhibition mechanism described byFarberof.