Affiliation:
1. John J. McKetta Department of Chemical Engineering The University of Texas at Austin Austin Texas 78712 USA
2. Department of Chemistry The University of Texas at Austin Austin Texas 78712 USA
3. Department of Geological Sciences Jackson School of Geosciences The University of Texas at Austin Austin Texas 78712 USA
Abstract
AbstractWhen investigating carbonaceous species on a catalyst via temperature‐programmed techniques, both the nature of the carbons and the possibility of the catalytic reaction of carbonaceous species should be considered. Here we examined CH4 decomposition (carbon deposition from CH4) and the reverse Boudouard reaction (carbon elimination by CO2) on the Ni/Al2O3 catalyst using sequential temperature‐programmed experiments. Carefully considering both the location and characteristics of carbon deposits formed on the Ni/Al2O3 catalyst, we conclude that carbons located on the Al2O3 support are challenging to remove by CO2 regardless of their nature, indicating the importance of support activity in reducing carbon deposits. In this study, the incorporation of cesium (Cs) into Al2O3 shows no effect on the prevention of carbon deposition from CH4 but does show an enhancement of carbon removal via the reverse Boudouard reaction, resulting in less coke formation on the Ni/Cs doped Al2O3 catalyst than the Ni/Al2O3 catalyst by 17 % for the dry reforming of methane.
Cited by
4 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献