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Tuning of active nickel species in MOF-derived nickel catalysts for the control on acetic acid steam reforming and hydrogen production

Authors
Kumar, AnkitVikrant, KumarYounis, Sherif A.Kim, Ki Hyun
Issue Date
May-2023
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
Nickel complex catalyst; Metal-organic framework; Hydrogen production; Acetic acid steam reforming; Reaction mechanism
Citation
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, v.48, no.40, pp.14964 - 14977
Indexed
SCIE
SCOPUS
Journal Title
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume
48
Number
40
Start Page
14964
End Page
14977
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/191079
DOI
10.1016/j.ijhydene.2023.01.036
ISSN
0360-3199
Abstract
Acetic acid (AcOH) steam reforming for hydrogen (H2) generation was investigated using a zero valent nickel complex (Ni-comp) derived from a metal-organic framework precursor supported over aluminum oxide/lanthanum oxide-cerium dioxide (ALC). The effects of Ni loading ratio (10, 15, and 20 wt%) on the catacatalytic activity were investigated in the range of 400 to 650 °C to H2 generation. The Ni-comp/ALC catalysts exhibited almost complete conversion of AcOH (XAcOH >98%) to H2 (XH2>90%) alongside some impurities (e.g., carbon monoxide, methane, and carbon dioxide). A maximum H2 yield (91.36% (0.064 mol-1 gcat−1 h−1)) was attained at the following conditions: 15 wt% Ni loading, steam to carbon molar ratio of 6.5, weight hourly space velocity of 1.05 h−1, and 600 °C. The 15 wt% Ni catalyst maintained sufficient stability over 40 h reaction time. Accordingly, Ni-comp-ALC interactions were seen to efficiently improve the activity and stability of the catalyst so as to synergistically resist coke deposition and metal sintering through the formation of a large number of free Ni particles and oxygen vacancies.
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