Abstract
Ni nanoparticles (around 4 nm diameter) were successfully supported on cage-type mesoporous silica SBA-16 (denoted as Ni@SBA-16) via wet impregnation at pH 9, followed by the calcination-reduction process. The Ni@SBA-16 catalyst with a very high Ni loading amount (22.9 wt %) exhibited exceptionally high CH4 selectivity for CO2 hydrogenation. At a nearly identical loading amount, the Ni@SBA-16 catalysts with smaller particle size of Ni NPs surprisingly exhibited a higher catalytic activity of CO2 hydrogenation and also led to a higher selectivity on CH4 formation than the Ni@SiO2 catalysts. This enhanced activity of the Ni@SBA-16 catalyst is suggested to be an accumulative result of the advantageous structural properties of the support SBA-16 and the well confined Ni NPs within the support; both induced a favorable reaction pathway for high selectivity of CH4 in CO2 hydrogenation.
| Original language | English |
|---|---|
| Pages (from-to) | 2326-2331 |
| Number of pages | 6 |
| Journal | ChemSusChem |
| Volume | 9 |
| Issue number | 17 |
| DOIs | |
| State | Published - 08 09 2016 |
Bibliographical note
Publisher Copyright:© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Keywords
- carbon dioxide
- hydrogenation
- mesoporous silica
- methane selectivity
- nickel