TY - JOUR
T1 - Light olefins synthesis from CO2 hydrogenation over mixed Fe–Co–K supported on micro-mesoporous carbon catalysts
AU - Witoon, Thongthai
AU - Numpilai, Thanapha
AU - Nueangnoraj, Khanin
AU - Cheng, Chin Kui
AU - Chareonpanich, Metta
AU - Limtrakul, Jumras
N1 - Funding Information:
This research was supported in part by the National Research Council of Thailand ( N41A640081 and N42A640324 for T.W. and M.C.), the Kasetsart University Research and Development Institute (KURDI) through its program of Development of Advance Researcher Competence System for Competitiveness in Agriculture and Food , and the Thailand Science Research and Innovation through its program of fundamental fund (FF(KU)21.65) .
Publisher Copyright:
© 2021 Hydrogen Energy Publications LLC
PY - 2022/12/30
Y1 - 2022/12/30
N2 - Recycling CO2 into light olefins is a promising approach to reduce CO2 emissions. To promote this technology, an efficient catalyst with high activity and selectivity towards light olefins is imperative. In this work, a series of Fe–Co–K supported on micro-mesoporous carbon (MMC) and microporous carbon (MC) with different metal loading contents (20–80 wt%) were prepared for CO2 hydrogenation to light olefins. Impregnating mixed metal oxides on both MMC and MC reduced particle sizes and enhanced their dispersion and reducibility, yielding a higher CO2 conversion compared to the unsupported Fe–Co–K catalyst. The metal oxides were highly dispersed inside the micropores of MC support, achieving the highest CO2 conversion. However, the high dispersion of metal oxides inside micropores led to the formation of isolated particles with a low interfacial contact with each other, resulting in a low light olefins selectivity. The MMC support provided a lower degree of metal dispersion, creating more interfacial contact area, promoting the selectivity towards olefins. Overall, the 60 wt% Fe–Co–K supported on MMC catalyst exhibited the highest light olefins yield of 10.8% at 400 °C and 20 bar and excellent stability.
AB - Recycling CO2 into light olefins is a promising approach to reduce CO2 emissions. To promote this technology, an efficient catalyst with high activity and selectivity towards light olefins is imperative. In this work, a series of Fe–Co–K supported on micro-mesoporous carbon (MMC) and microporous carbon (MC) with different metal loading contents (20–80 wt%) were prepared for CO2 hydrogenation to light olefins. Impregnating mixed metal oxides on both MMC and MC reduced particle sizes and enhanced their dispersion and reducibility, yielding a higher CO2 conversion compared to the unsupported Fe–Co–K catalyst. The metal oxides were highly dispersed inside the micropores of MC support, achieving the highest CO2 conversion. However, the high dispersion of metal oxides inside micropores led to the formation of isolated particles with a low interfacial contact with each other, resulting in a low light olefins selectivity. The MMC support provided a lower degree of metal dispersion, creating more interfacial contact area, promoting the selectivity towards olefins. Overall, the 60 wt% Fe–Co–K supported on MMC catalyst exhibited the highest light olefins yield of 10.8% at 400 °C and 20 bar and excellent stability.
KW - CO hydrogenation
KW - Fe-based catalysts
KW - Light olefins
KW - Micro-mesoporous carbon
KW - Microporous carbon
UR - http://www.scopus.com/inward/record.url?scp=85119616208&partnerID=8YFLogxK
U2 - 10.1016/j.ijhydene.2021.10.265
DO - 10.1016/j.ijhydene.2021.10.265
M3 - Article
AN - SCOPUS:85119616208
SN - 0360-3199
VL - 47
SP - 42185
EP - 42199
JO - International Journal of Hydrogen Energy
JF - International Journal of Hydrogen Energy
IS - 100
ER -