TY - JOUR
T1 - Highly selective CuO-ZnO@Cu-MOR catalysts prepared by ultrafast solid processing for carbon dioxide hydrogenation to methanol
AU - Wei, Yayu
AU - Peng, Bo
AU - Li, Yanhong
AU - Xu, Run
AU - Huang, Aisheng
N1 - Publisher Copyright:
© 2024 Elsevier Inc.
PY - 2024/6/15
Y1 - 2024/6/15
N2 - The conversion of CO2 into methanol has emerged as a promising strategy for addressing climate change and optimizing the utilization of carbon resources. Conventional synthesis methods for Cu-based catalysts, such as co-precipitation, necessitate the consumption of substantial amounts of solvent and meticulous control over preparation conditions, while also being susceptible to deactivation by water during hydrogenation. Therefore, it is crucial to develop a catalyst that can be readily synthesized and exhibits outstanding performance and durability. In this study, we present an ultrafast (only 20 min), solid-phase grinding approach to fabricate CuO-ZnO@Cu-MOR catalysts for CO2 hydrogenation to methanol. The resulting catalysts were comprehensively characterized using XRD, XPS, H2-TPR, NH3-TPD, SEM, HRTEM, and In-situ-FTIR techniques. Notably, the CuO-ZnO@Cu-MOR catalysts with a distinctive capsule-like structure displayed a high catalytic performance for CO2 hydrogenation. The byproducts of methane and water produced by the CO2 hydrogenation process were able to be further converted to methanol through Cu-MOR, leading to a significant enhancement of the methanol selectivity (95.6 %) and CO2 conversion (22.8 %). Moreover, a long-term test lasting 300 h demonstrated constant catalytic performances and superior durability.
AB - The conversion of CO2 into methanol has emerged as a promising strategy for addressing climate change and optimizing the utilization of carbon resources. Conventional synthesis methods for Cu-based catalysts, such as co-precipitation, necessitate the consumption of substantial amounts of solvent and meticulous control over preparation conditions, while also being susceptible to deactivation by water during hydrogenation. Therefore, it is crucial to develop a catalyst that can be readily synthesized and exhibits outstanding performance and durability. In this study, we present an ultrafast (only 20 min), solid-phase grinding approach to fabricate CuO-ZnO@Cu-MOR catalysts for CO2 hydrogenation to methanol. The resulting catalysts were comprehensively characterized using XRD, XPS, H2-TPR, NH3-TPD, SEM, HRTEM, and In-situ-FTIR techniques. Notably, the CuO-ZnO@Cu-MOR catalysts with a distinctive capsule-like structure displayed a high catalytic performance for CO2 hydrogenation. The byproducts of methane and water produced by the CO2 hydrogenation process were able to be further converted to methanol through Cu-MOR, leading to a significant enhancement of the methanol selectivity (95.6 %) and CO2 conversion (22.8 %). Moreover, a long-term test lasting 300 h demonstrated constant catalytic performances and superior durability.
KW - CO hydrogenation
KW - CO utilization
KW - Methanol preparation
KW - Mordenite zeolite
KW - Solid-phase grinding synthesis
UR - https://www.scopus.com/pages/publications/85190762949
U2 - 10.1016/j.micromeso.2024.113140
DO - 10.1016/j.micromeso.2024.113140
M3 - 文章
AN - SCOPUS:85190762949
SN - 1387-1811
VL - 374
JO - Microporous and Mesoporous Materials
JF - Microporous and Mesoporous Materials
M1 - 113140
ER -