催化学报 ›› 2012, Vol. 33 ›› Issue (4): 610-620.DOI: 10.1016/S1872-2067(11)60351-3

• 研究论文 • 上一篇    下一篇

二乙醇胺作添加剂 Ru-Zn 催化剂上苯选择加氢制环己烯

孙海杰, 潘雅洁, 王红霞, 董英英, 刘仲毅*, 刘寿长   

  1. 郑州大学化学系, 河南郑州450001
  • 收稿日期:2011-10-21 修回日期:2011-11-21 出版日期:2012-04-13 发布日期:2015-09-09

Selective Hydrogenation of Benzene to Cyclohexene over a Ru-Zn Catalyst with Diethanolamine as an Additive

SUN Haijie, PAN Yajie, WANG Hongxia, DONG Yingying, LIU Zhongyi*, LIU Shouchang   

  1. Department of Chemistry, Zhengzhou University, Zhengzhou 450001, Henan, China
  • Received:2011-10-21 Revised:2011-11-21 Online:2012-04-13 Published:2015-09-09

摘要: 采用共沉淀法制备了 Ru-Zn 催化剂, 考察了二乙醇胺的添加对 Ru-Zn 催化剂上苯选择加氢制环己烯性能的影响, 并采用 N2 物理吸附、透射电镜、X 射线衍射、X 射线荧光、傅里叶变换红外和程序升温还原等手段对催化剂进行了表征. 结果表明, 二乙醇胺可以与浆液中 ZnSO4 反应生成 (Zn(OH)2)3(ZnSO4)(H2O)3和硫酸二乙醇胺盐. 随着二乙醇胺用量的增加, 化学吸附在催化剂表面的 (Zn(OH)2)3(ZnSO4)(H2O)3 增多, 它与硫酸二乙醇胺盐的协同作用提高了 Ru-Zn(4.9%) 催化剂上苯选择加氢生成环己烯的选择性. 当二乙醇胺用量为 0.3 g 时, ((Zn(OH)2)3(ZnSO4)(H2O)3在 Ru-Zn(4.9%) 催化剂加氢后样品的表面高度分散, 反应性能最佳, 循环使用第 3 次时苯转化率为 84.3%, 环己烯选择性和收率分别达 75.5% 和 63.6%; 使用至第 4 次时, 反应 25 min 时苯转化率和环己烯选择性仍可达 75% 以上, 环己烯收率为 58% 以上.

关键词: 二乙醇胺, 钌, 锌, 苯, 选择加氢, 环己烯

Abstract: A Ru-Zn catalyst was prepared by co-precipitation, and the effect of adding diethanolamine on benzene selective hydrogenation to cyclohexene was investigated. The catalyst was characterized by N2 physisorption, transmission electron microscopy, X-ray diffraction, X-ray fluorescence, Fourier transform infrared spectra, and temperature-programmed reduction. Diethanolamine reacted with ZnSO4 in the slurry to form (Zn(OH)2)3(ZnSO4)(H2O)3 and diethanolamine sulfate. The amount of (Zn(OH)2)3(ZnSO4)(H2O)3 adsorbed on the catalyst surface increased with the increase of diethanolamine amount. The synergism of (Zn(OH)2)3(ZnSO4)(H2O)3 and diethanolamine sulfate improved the cyclohexene selectivity of the Ru-Zn(4.9%) catalyst. With a diethanolamine dosage of 0.3 g, (Zn(OH)2)3(ZnSO4)(H2O)3 was highly dispersed on the catalyst surface and the sample after hydrogenation was characterized, and this catalyst exhibited the best performance with a cyclohexene selectivity and yield of 75.5% and 63.6%, respectively, at the benzene conversion of 84.3% in the third run. Moreover, the benzene conversion and cyclohexene selectivity were stable above 75% and cyclohexene yields were above 58% in fourth run.

Key words: diethanolamine, ruthenium, zinc, benzene, selective hydrogenation, cyclohexene