甲烷化
甲醇
催化作用
氢
氢溢流
化学
甲醇重整装置
无机化学
二氧化碳
化学工程
制氢
合成气
有机化学
蒸汽重整
工程类
作者
Tomoyuki Inui,Tatsuya Takeguchi
出处
期刊:Catalysis Today
[Elsevier BV]
日期:1991-08-01
卷期号:10 (1): 95-106
被引量:163
标识
DOI:10.1016/0920-5861(91)80077-m
摘要
Abstract Recent studies on effective catalytic conversion of carbon dioxide to hydrocarbons were summarized. Firstly, requisites of catalyst structure to realize rapid methanation of carbon dioxide were investigated in detail. The support having a meso-macro bimodal pore structure was found to be superior for both diffusion rates of reactants and products and high dispersion of active catalyst substances, respectively. The Ni-based composite catalyst combined with a small amount of La2O3 and a very small amount of Ru exhibited a very high methanation rate. The role of Ru in the composite catalyst was elucidated as the portholes of hydrogen spillover for the active sites in Ni part. Next, CuZnCrAl mixed oxide catalysts were synthesized by the intrinsic uniform gelation method to synthesize methanol with a comparable reaction rate of syngas conversion to methanol. Furthermore, the performance of methanol synthesis catalyst was markedly improved by modification with Pd or Ag as anticipated an effect of spillover. Gasoline synthesis from carbon dioxide and hydrogen was firstly achieved by adopting a two-stage reactor connected in a series manner as follows; in the first reactor the modified methanol synthesis catalyst was packed, and in the second reactor an HFesilicate catalyst, which has the ZSM-5 (MFI) structure and the activity of methanol to gasoline conversion without acceptance of any effect from the unconverted hydrogen, was packed.
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