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Highly Active Sm 2 O 3 ‐Ni Xerogel Catalysts for CO 2 Methanation
Author(s) -
Ilsemann Jan,
Sonström Andrea,
Gesing Thorsten M.,
Anwander Reiner,
Bäumer Marcus
Publication year - 2019
Publication title -
chemcatchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.497
H-Index - 106
eISSN - 1867-3899
pISSN - 1867-3880
DOI - 10.1002/cctc.201802049
Subject(s) - methanation , catalysis , physisorption , materials science , transition metal , heterogeneous catalysis , temperature programmed reduction , inorganic chemistry , chemical engineering , chemistry , organic chemistry , engineering
We report on a new synthesis route for pure Sm 2 O 3 and Sm 2 O 3 ‐Ni xerogels by modifying the well‐known epoxide addition method. The resulting xerogels are used to prove the suitability of samaria as a highly effective catalyst support and to determine the optimal Ni loading. Therefore, a set of five catalysts with Ni loadings between 4 wt % and 89 wt % Ni was prepared and fully characterized by X‐ray diffraction, N 2 physisorption, transmission electron microscopy and H 2 temperature‐programmed reduction. Catalytic measurements reveal that the catalyst with 39 wt % Ni shows the best catalytic performance, outperforming even highly active literature known systems. Stability runs indicate that the catalyst deactivates independently of the Ni loading as well as conversion level over 600 min due to, most likely, carbonate formation. This deactivation, however, is reversible by a simple regeneration step. As shown by simultaneous CO 2 /CO methanation measurements, the Ni−Sm 2 O 3 catalysts are also highly efficient for CO methanation. In this case, CO is preferentially converted to methane compared to CO 2 .