Oxygen Vacancy-Mediated Selective H2S Oxidation over Co-Doped LaFexCo1−xO3 Perovskite

Compared to the Claus process, selective H2S catalytic oxidation to sulfur is a promising reaction, as it is not subject to thermodynamic limitations and could theoretically achieve ~100% H2S conversion to sulfur. In this study, we investigated the effects of Co and Fe co-doping in ABO3 perovskite o...

Full description

Saved in:
Bibliographic Details
Published inCatalysts Vol. 12; no. 2; p. 236
Main Authors Yu, Xinlei, Tao, Xun, Gao, Yunfei, Ding, Lu, Wang, Yanqin, Yu, Guangsuo, Wang, Fuchen
Format Journal Article
LanguageEnglish
Published Basel MDPI AG 19.02.2022
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Compared to the Claus process, selective H2S catalytic oxidation to sulfur is a promising reaction, as it is not subject to thermodynamic limitations and could theoretically achieve ~100% H2S conversion to sulfur. In this study, we investigated the effects of Co and Fe co-doping in ABO3 perovskite on H2S selective catalytic oxidation. A series of LaFexCo1−xO3 (x = 0, 0.2, 0.4, 0.6, 0.8, 1.0) perovskites were synthesized by the sol-gel method. Compared to LaFeO3 and LaCoO3, co-doped LaFexCo1−xO3 significantly improved the H2S conversion and sulfur selectivity at a lower reaction temperature. Nearly 100% sulfur yield was achieved on LaFe0.4Co0.6O3 under 220 °C with exceptional catalyst stability (above 95% sulfur yield after 77 h). The catalysts were characterized by XRD, BET, FTIR, XPS, and H2-TPR. The characterization results showed that the structure of LaFexCo1−xO3 changed from the rhombic phase of LaCoO3 to the cubic phase of LaFeO3 with Fe substitution. Doping with appropriate iron (x = 0.4) facilitates the reduction of Co ions in the catalyst, thereby promoting the H2S selective oxidation. This study demonstrates a promising approach for low-temperature H2S combustion with ~100% sulfur yield.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ISSN:2073-4344
2073-4344
DOI:10.3390/catal12020236