TY - JOUR
T1 - Role of lanthanum oxycarbonate in dendritic fibrous Ni/CHE-La catalyst on enhanced CO2dissociation for low-Temperature CO2reforming of methane
AU - Liew, Shi Yan
AU - Jalil, Aishah Abdul
AU - Siang, Tan Ji
AU - Aziz, Fazilah Farhana Abdul
AU - Fauzi, Anees Ameera
AU - Jusoh, Nurfatehah Wahyuny Che
AU - Teh, Lee Peng
AU - Rajendran, Saravanan
N1 - Publisher Copyright:
© 2025 Elsevier Ltd.
PY - 2025/10
Y1 - 2025/10
N2 - Catalyst design of low temperature CO2 reforming of methane for sustainable energy production is essential to overcome the activation energy barrier of its stable CO2 and CH4 reactant gases, metal sintering and coke poisoning. Herein, we report the development of fibrous lanthanum silica synthesized via microemulsion seed crystallization loaded with nickel oxide metal through wetness impregnation (Ni/CHE-La). The incorporation of lanthanum in the fibrous dendritic Ni/CHE-La reportedly contributed to strong metal-support interaction benefiting its metal anti-sintering properties as proven by FTIR spectroscopy, H2-TPR, HRTEM and XPS. Ni/CHE-La was also compared with Ni/KCC-1 and structurally unmodified Ni/SiLa to determine the content of surface reactive oxygen species and its influence on its catalytic activity under integral reaction conditions in the temperature interval of 400-800 °C. The XPS measurements demonstrated the amount of surface reactive oxygen associated as oxygen vacancies decreases in the following order (Ni/CHE-La > Ni/KCC-1> Ni/SiLa). The catalytic activity of all three catalysts followed similar trend, highlighting the synergistic benefits of lanthanum oxycarbonate and surface reactive oxygen species on the fibrous lanthanum silica promoted the dissociation of CO2 into CO and lowered the CH4 apparent activation energy barrier. The regeneration study showed Ni/CHE-La possessed a highly stable reaction after 18h at 600 °C. Further post-reaction study revealed its high anti-sintering resistance and anti-coking properties which could be assigned to the enhanced CO2 dissociation driven by lanthanum oxycarbonate phase on the catalytic surface for the removal of carbon deposits.
AB - Catalyst design of low temperature CO2 reforming of methane for sustainable energy production is essential to overcome the activation energy barrier of its stable CO2 and CH4 reactant gases, metal sintering and coke poisoning. Herein, we report the development of fibrous lanthanum silica synthesized via microemulsion seed crystallization loaded with nickel oxide metal through wetness impregnation (Ni/CHE-La). The incorporation of lanthanum in the fibrous dendritic Ni/CHE-La reportedly contributed to strong metal-support interaction benefiting its metal anti-sintering properties as proven by FTIR spectroscopy, H2-TPR, HRTEM and XPS. Ni/CHE-La was also compared with Ni/KCC-1 and structurally unmodified Ni/SiLa to determine the content of surface reactive oxygen species and its influence on its catalytic activity under integral reaction conditions in the temperature interval of 400-800 °C. The XPS measurements demonstrated the amount of surface reactive oxygen associated as oxygen vacancies decreases in the following order (Ni/CHE-La > Ni/KCC-1> Ni/SiLa). The catalytic activity of all three catalysts followed similar trend, highlighting the synergistic benefits of lanthanum oxycarbonate and surface reactive oxygen species on the fibrous lanthanum silica promoted the dissociation of CO2 into CO and lowered the CH4 apparent activation energy barrier. The regeneration study showed Ni/CHE-La possessed a highly stable reaction after 18h at 600 °C. Further post-reaction study revealed its high anti-sintering resistance and anti-coking properties which could be assigned to the enhanced CO2 dissociation driven by lanthanum oxycarbonate phase on the catalytic surface for the removal of carbon deposits.
KW - Active oxygen species
KW - Carbon dioxide reforming of methane
KW - CO2 conversion
KW - Fibrous silica
KW - Lanthanum oxide
UR - https://www.scopus.com/pages/publications/105011257653
U2 - 10.1016/j.jece.2025.117626
DO - 10.1016/j.jece.2025.117626
M3 - Article
AN - SCOPUS:105011257653
SN - 2213-2929
VL - 13
JO - Journal of Environmental Chemical Engineering
JF - Journal of Environmental Chemical Engineering
IS - 5
M1 - 117626
ER -