物理化学学报 >> 1997, Vol. 13 >> Issue (12): 1057-1060.doi: 10.3866/PKU.WHXB19971201

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碳纳米管负载铑催化剂上丙烯氢甲酰化

张宇,吴氾昕,张鸿斌,林国栋,袁友珠,蔡启瑞   

  1. 厦门大学化学系,固体表面物理化学国家重点实验室,厦门 361005
  • 收稿日期:1997-08-26 修回日期:1997-09-26 发布日期:1997-12-15
  • 通讯作者: 张鸿斌

Hydroformylation of Propene over Carbon Nanotubes-Supported Rh-Catalyst

Zhang Yu,Wu Fan-Xin,Zhang Hong-Bin,Lin Guo-Dong,Yuan You-Z   

  1. Department of Chemistry State Key Laboratory for Physical Chemistry of the Solid Surface,Xiamen University,Xiamen 361005
  • Received:1997-08-26 Revised:1997-09-26 Published:1997-12-15
  • Contact: Zhang Hong-Bin

关键词: 碳纳米管载体材料, 氢甲酰化, 丙烯, 负载型铑催化剂

Abstract:

Effect of carbon nanotubes, as a novel support material, on the performance of Rh-catalyst supported by them was studied. Catalysts based on carbon nanotubes, SiO2, carbon molecular sieves, active carbon, and GDX-l02(a copolymer of styrene with divinylbenzene),were prepared, and their catalytic behaviors for propene hydroformylation were investigated and compared. The results showed that, over the carbon nanotubes-supported Rh-catalyst, C3H6 conversion and regioselectivity of butyric aldehyde (represented by n/i, a ratio of n-butyric aldehyde to its isomer, i-butyric aldehyde, in the products) were pronouncedly improved: the average turnover frequency(TOF) for the catalytic hydroformylation of propene was 0.079 s-1 at 393K, which was 2.1 times faster than that over the Rh catalyst based on SiO2, and the n/i ratio of the aldehyde products reached to 11.6, which was 1.9 times higher than that over the catalyst based on SiO2. The roles of six-membered C-ring at the surface of the carbon-nanotubes on the stability of the catalytically active Rh-complexes and of the tubular nano-channel on the spatiospecific seletivity of reaction intermediate state and butyric aldehyde produced were discussed.

Key words: Carbon-nanotubes support material, Hydroformylation, Propene, Supported Rh-catalyst