Physico-chemical investigation of catalytic oxidation sites in 4%Rh/CeO2 catalysts prepared by impregnation and deposition–precipitation methods

Madona Labaki, S. Aouad, Sara Hany, Cynthia Abou Serhal, Edmond Abi-Aad, Antoine Aboukaïs

Research output: Contribution to journalArticlepeer-review

Abstract

4 wt% Rh/CeO2 catalysts were prepared by two different methods: deposition–precipitation (DP) and impregnation (Imp). X-ray diffraction (XRD), differential scanning calorimetry and thermogravimetry (DSC-TG), temperature-programmed reduction (TPR), and electron paramagnetic resonance (EPR) were used for physicochemical characterization. The solids were tested in propylene and carbon black oxidation reactions. The 4%Rh/CeO2 (DP) showed better catalytic performance in both reactions compared to the catalyst prepared by the impregnation method. The XRD technique evidenced the formation of Rh2O3 phase in the DP-solid after calcination of this latter at 400 °C for 4 h. EPR evidenced, only in the DP-solid, the presence of O2 species in interaction with the CeO2 surface whereas Rh4+ ions in the form of clusters were identified in both solids. The TPR technique showed that the DP-solid was reduced by hydrogen at lower temperature compared to the impregnated one. The higher catalytic performance of the DP-solid was attributed to the presence of O2 species along with the presence of Rh2O3 phase in ceria and to the better reducibility and lower particle size of the rhodium species.

Original languageEnglish (US)
Article number110472
JournalChemical Physics
Volume527
DOIs
StatePublished - Nov 1 2019

Keywords

  • CeO
  • Deposition–precipitation
  • Impregnation
  • O
  • Oxidation
  • RhO

ASJC Scopus subject areas

  • General Physics and Astronomy
  • Physical and Theoretical Chemistry

Fingerprint

Dive into the research topics of 'Physico-chemical investigation of catalytic oxidation sites in 4%Rh/CeO2 catalysts prepared by impregnation and deposition–precipitation methods'. Together they form a unique fingerprint.

Cite this