TY - JOUR
T1 - Optimizing hydrogen production: influence of promoters in methane decomposition on titania-modified-zirconia supported fe catalyst
AU - Al-Fatesh, Ahmed S.
AU - Vadodariya, Dharmesh M.
AU - Bayazed, Mohammed O.
AU - Osman, Ahmed I.
AU - Ibrahim, Ahmed Aidid
AU - Fakeeha, Anis Hamza
AU - Alanazi, Yousef M.
AU - Abasaeed, Ahmed E.
AU - Kumar, Rawesh
PY - 2024/5/7
Y1 - 2024/5/7
N2 - This study addresses the pivotal challenge of hydrogen production through methane decomposition, offering a pathway to achieving clean energy goals. Investigating the utilization of titania-modified zirconia dual redox supports (10TiZr) in iron or doped iron-based catalysts for the CH4 decomposition reaction, our research involves a thorough characterization process. This includes analyses of the surface area porosity, X-ray diffraction, Raman-infrared spectroscopy, and temperature-programmed reduction/oxidation. The observed sustained enhancement in catalytic activity over extended durations suggests the in situ formation of catalytically active sites. The introduction of Co or Ni into the 30Fe/10TiZr catalyst leads to the generation of a higher density of reducible species. Furthermore, the Ni-promoted 30Fe/10TiZr catalyst exhibits a lower crystallinity, indicating superior dispersion. Notably, the cobalt-promoted 30Fe/10TiZr catalyst achieves over 80% CH4 conversion and H2 yield within 3 h. Additionally, the Ni-promoted 30Fe/10TiZr catalyst attains a remarkable 87% CH4 conversion and 82% H2 yield after 3 h of the continuous process.
AB - This study addresses the pivotal challenge of hydrogen production through methane decomposition, offering a pathway to achieving clean energy goals. Investigating the utilization of titania-modified zirconia dual redox supports (10TiZr) in iron or doped iron-based catalysts for the CH4 decomposition reaction, our research involves a thorough characterization process. This includes analyses of the surface area porosity, X-ray diffraction, Raman-infrared spectroscopy, and temperature-programmed reduction/oxidation. The observed sustained enhancement in catalytic activity over extended durations suggests the in situ formation of catalytically active sites. The introduction of Co or Ni into the 30Fe/10TiZr catalyst leads to the generation of a higher density of reducible species. Furthermore, the Ni-promoted 30Fe/10TiZr catalyst exhibits a lower crystallinity, indicating superior dispersion. Notably, the cobalt-promoted 30Fe/10TiZr catalyst achieves over 80% CH4 conversion and H2 yield within 3 h. Additionally, the Ni-promoted 30Fe/10TiZr catalyst attains a remarkable 87% CH4 conversion and 82% H2 yield after 3 h of the continuous process.
U2 - 10.1021/acsomega.4c00729
DO - 10.1021/acsomega.4c00729
M3 - Article
AN - SCOPUS:85191831300
SN - 2470-1343
VL - 9
SP - 20322
EP - 20330
JO - ACS Omega
JF - ACS Omega
IS - 18
ER -