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Effect of NaOH Concentration on Rapidly Quenched Cu–Al Alloy-Derived Cu Catalyst for CO 2 Hydrogenation to CH 3 OH.

Authors :
Liu, Xuancheng
Sun, Dong
Ji, Yushan
Zu, Sijie
Pei, Yan
Yan, Shirun
Qiao, Minghua
Zhang, Xiaoxin
Zong, Baoning
Source :
Catalysts (2073-4344). Jun2024, Vol. 14 Issue 6, p391. 13p.
Publication Year :
2024

Abstract

By utilizing greenhouse gas CO2 and renewable energy-sourced H2 to produce methanol, the "methanol economy" can replace fossil fuels and H2 as the energy storage medium, which not only reduces CO2 emissions, but also mitigates the energy shortage issue. However, the traditional Cu-based catalysts for CO2-to-methanol conversion suffer from low activity at low temperature and high vulnerability to sintering and deactivation. In this contribution, rapidly quenched skeletal Cu catalysts (RQ Cu) are prepared by leaching the RQ Cu–Al alloy with NaOH aqueous solutions of different concentrations. It is found that high NaOH concentration of 10 wt% favors the preparation of the RQ Cu-10 catalyst with higher porosity, lower residual Al content, and larger active Cu surface area (SCu) than the RQ Cu-3 catalyst leached with 3 wt% of NaOH solution. However, in aqueous-phase CO2 hydrogenation at 473 K and 4.0 MPa, the CO2 conversion over the RQ Cu-3 catalyst is more than two times greater than that over the RQ Cu-10 catalyst, and the selectivity and productivity of methanol are 1.20 and 2.69 times of the corresponding values over the RQ Cu-10 catalyst. At 5.0 MPa, the selectivity and productivity of methanol are further boosted to 97.9% and 1.329 mmol gCu–1 h–1 on the RQ Cu-3 catalyst. It is identified that the SCu of the RQ Cu-3 catalyst is well preserved after reaction, while dramatic growth of the Cu crystallites occurs for the RQ Cu-10 catalyst. The better catalytic performance and stability of the RQ Cu-3 catalyst are tentatively attributed to the presence of more residual Al species by using NaOH solution with lower concentration for Al leaching, which acts as the dispersant for the Cu crystallites during the reaction. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20734344
Volume :
14
Issue :
6
Database :
Academic Search Index
Journal :
Catalysts (2073-4344)
Publication Type :
Academic Journal
Accession number :
178160290
Full Text :
https://doi.org/10.3390/catal14060391