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Highly efficient steam reforming of ethanol (SRE) over CeO x grown on the nano Ni x Mg y O matrix: H 2 production under a high GHSV condition
Author(s) -
Luo Xiang,
Hong Yu,
Zhang Honglei,
Shi Kaiqi,
Yang Gang,
Wu Tao
Publication year - 2019
Publication title -
international journal of energy research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.808
H-Index - 95
eISSN - 1099-114X
pISSN - 0363-907X
DOI - 10.1002/er.4549
Subject(s) - catalysis , steam reforming , water gas shift reaction , space velocity , x ray photoelectron spectroscopy , hydrogen production , hydrogen , chemical engineering , materials science , noble metal , nickel , temperature programmed reduction , yield (engineering) , chemistry , adsorption , inorganic chemistry , metallurgy , selectivity , organic chemistry , engineering
Summary Steam reforming of ethanol (SRE) over non‐noble metal catalysts is normally conducted at high temperature (>600°C) to thermodynamically favour the catalytic process and carbon deposition mitigation. However, high temperature inhibits water‐gas shift reaction (WGSR) and therefore restrains the yield of H 2 and leads to the formation of an excessive amount of CO. The modification of non‐noble metal catalyst to enhance WGSR is an attractive alternative. In this study, CeO x was firstly loaded onto a nano‐scaled Ni x Mg y O matrix and subsequently used as the catalyst for hydrogen production via SRE. Morphology of the catalyst materials was characterized by using a series of technologies, while H 2 ‐temperature programmed reduction (H 2 ‐TPR), CO‐temperature programmed deposition (CO‐TPD), and X‐ray photoelectron spectroscopy (XPS), were employed to study the surface nickel, ceria clusters, and their interactions. The catalytic activity and durability of the catalyst were studied in the temperature region of 500°C to 800°C. The CeO x ‐coated nano Ni x Mg y O matrix exhibited an outstanding hydrogen yield of 4.82 mol/mol ethanol under a high gas hourly space velocity (GHSV) of 200 000 hour −1 . It is found that the unique Ni 0 ‐CeO x structure facilitates the adsorption of CO on the surface and therefore promotes the effective hydrogen production via WGSR. Moreover, this modified Ni x Mg y O matrix was found to be a more robust and anticoking nanocatalyst because of reversible switch between Ce 4+ and Ce 3+ .