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MoO x ‐Doped Ordered Mesoporous Ni/Al 2 O 3 Catalyst for CO Methanation
Author(s) -
Zhang Yang,
Yang Hongyuan,
Liu Qing,
Bian Bing
Publication year - 2020
Publication title -
energy technology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.91
H-Index - 44
eISSN - 2194-4296
pISSN - 2194-4288
DOI - 10.1002/ente.202000165
Subject(s) - methanation , catalysis , mesoporous material , materials science , space velocity , particle size , scanning electron microscope , nickel , sintering , chemical engineering , inorganic chemistry , analytical chemistry (journal) , chemistry , metallurgy , selectivity , composite material , organic chemistry , engineering
To address the problems of sintering of Ni particles and poor low‐temperature activity of Ni‐based catalysts for CO methanation, MoO x ‐doped ( x < 3) ordered mesoporous Ni/Al 2 O 3 catalysts are prepared by two different methods, including the impregnation method and evaporation‐induced self‐assembly (EISA) method. The samples before and after the catalytic reaction are thoroughly characterized by scanning electron microscopy and transmission electron microscopy. The ordered mesoporous structure is retained in all catalysts, whereas the ones prepared by the EISA method demonstrate high specific surface area, small Ni particle size, and high metal dispersion. After reduction in H 2 flow, the Mo promoter is in the form of MoO x ( x < 3) with the mixed valence of Mo (IV) and Mo (VI), which can increase the density of Ni atomic electron clouds and reduce the Ni particle size. The optimal mesoporous Ni‐Mo/Al 2 O 3 catalyst reaches the maximum CO conversion and CH 4 yield of 97.9% and 93.8%, respectively, at 375 °C, 0.1 MPa, and a weight hourly space velocity of 60 000 mL g −1 h −1 . In addition, this catalyst demonstrates excellent stability in 100 h‐lifetime test at high space velocity owing to the confinement of the ordered mesoporous structure and the addition of MoO x promoter.