Back to Search
Start Over
Indium-Promoted ZnZrOxSolid Solution Catalyst for CO2Hydrogenation to Methanol
- Source :
- Industrial & Engineering Chemistry Research; May 2024, Vol. 63 Issue: 20 p9026-9037, 12p
- Publication Year :
- 2024
-
Abstract
- Methanol synthesis is one of the most important and industrially viable approaches to carbon dioxide (CO2) utilization. Both the ZnZrOx(ZZO) solid solution catalyst and the In2O3catalyst have garnered extensive attention for their high methanol selectivity and excellent resistance to sintering and sulfur in CO2hydrogenation. Herein, a ZZO solid solution with a large surface area is selected as the carrier, and the supported In2O3strongly interacts with the ZZO to boost the generation of more oxygen vacancies on the ZZO surface that catalyzes methanol production. On incorporating an appropriate amount of In2O3(In 2.5 wt %) onto the ZZO catalyst, In2.5/ZZO exhibits markedly enhanced methanol production with a CO2conversion rate of 13.5% and a methanol space-time yield of 0.749 g gcat–1h–1at 330 °C, 5 MPa, and 24,000 mL gcat–1h–1. In situdiffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) reveals that the incorporated indium species facilitate hydrogen activation to increase the availability of surface hydrogen. The surface hydrogen is transferred to the active sites due to hydrogen spillover, facilitating the formation of HCOO* intermediates and boosting the hydrogenation of CO2to methanol. Theoretical analysis allows the rationalization of the observed improvement in the catalytic performance of the In2.5/ZZO catalyst. In2.5/ZZO showed excellent stability for up to 200 h on stream, demonstrating its potential as a practical catalyst for the hydrogenation of CO2to methanol.
Details
- Language :
- English
- ISSN :
- 08885885 and 15205045
- Volume :
- 63
- Issue :
- 20
- Database :
- Supplemental Index
- Journal :
- Industrial & Engineering Chemistry Research
- Publication Type :
- Periodical
- Accession number :
- ejs66269514
- Full Text :
- https://doi.org/10.1021/acs.iecr.4c00953