Effect of CeO2 on carbon deposition resistance of Ni/CeO2 catalyst supported on SiC porous ceramic for ethanol steam reforming

Ni/CeO2 catalysts (nCeO2:nNi = 0, 1, 4, 7, 10) supported on SiC porous ceramics for ethanol steam reforming (ESR) were investigated with respect to hydrogen production performance and growth of carbon deposition. The oxygen released from CeO2 enables the oxidation of CHx species to serve as carbon precursors, thus providing Ni/CeO2 catalysts with stronger resistance to carbon deposition compared with Ni catalysts. The Ni/CeO2 catalysts prepared by inverse microemulsion and impregnation methods exhibit regular semicircular spherical shape on SiC porous ceramics. Under 500 degrees C for 25 h of ESR re-action, the ethanol conversion rate over Ni/CeO2 catalysts (nCeO2:nNi = 7) is sustained up to 100% and H2 selectivity is essentially kept at 74%. The by-product selectivity declines stepwise with increasing content of CeO2, which is attributed to the adsorption and oxidation of CO and of CHx species as CH4 precursor from CeO2. The scanning electron microscopy (SEM) and transform electron microscopy (TEM) results reveal that further loading of CeO2 on the surface of Ni catalysts can alleviate both migration and sin -tering of Ni particles. Furthermore, carbon deposition on Ni/CeO2 catalysts preferentially outgrow fila-mentous rather than amorphous carbon, with a tendency for the latter to be more deactivated. (c) 2022 Chinese Society of Rare Earths. Published by Elsevier B.V. All rights reserved.

Automated summary

Ni/CeO2 catalysts supported on SiC porous ceramics were studied for ethanol steam reforming process. The presence of CeO2 improved the resistance to carbon deposition compared to Ni catalysts. The catalysts prepared by microemulsion and impregnation methods exhibited a regular semicircular spherical shape. Under ESR conditions, the ethanol conversion rate remained at 100% and H2 selectivity was maintained at 74% for Ni/CeO2 catalysts with a CeO2:Ni ratio of 7. The selectivity of by-products decreased gradually with increasing CeO2 content due to the adsorption and oxidation of CO and CHx species by CeO2.