Enhancement of surface morphology and catalytic kinetics of NiAl2O4 spinel-derived Ni catalyst to promote dry reforming of methane at low temperature for the direct application to a solid oxide fuel cell

Yonggyun Bae, Jongsup Hong

Research output: Contribution to journalArticlepeer-review

10 Citations (Scopus)

Abstract

Dry reforming of methane at low temperatures of 400 ∼ 700 °C is examined by using conventional Ni/Al2O3 catalyst and spinel-derived Ni catalyst anchored on aluminum oxide through powder-based solid-state reaction. The spinel-derived Ni catalyst exhibits uniform particle distribution with a size of 10 nm (10 times smaller than the conventional Ni/Al2O3 catalyst) and the highest catalytic performance under all operating conditions with apparent activation energies of 42.51 kJ/mol for CH4 conversion and 45.39 kJ/mol for CO2 conversion. Kinetics analysis elucidates that the conventional Ni/Al2O3 catalyst changes its rate-limiting factor from diffusion limitation to kinetics limitation with decreasing temperature near 550 °C. In contrast, the spinel-derived Ni catalyst has a single rate-limiting factor of diffusion limitation at all temperatures avoiding surface kinetics limitation. In addition, it is shown that the spinel-derived Ni catalyst exhibits better stability than the conventional Ni/Al2O3 catalyst, attributed to the enhanced interaction between active Ni particles and Al2O3 support.

Original languageEnglish
Article number136978
JournalChemical Engineering Journal
Volume446
DOIs
Publication statusPublished - 2022 Oct 15

Bibliographical note

Publisher Copyright:
© 2022

All Science Journal Classification (ASJC) codes

  • Chemistry(all)
  • Environmental Chemistry
  • Chemical Engineering(all)
  • Industrial and Manufacturing Engineering

Fingerprint

Dive into the research topics of 'Enhancement of surface morphology and catalytic kinetics of NiAl2O4 spinel-derived Ni catalyst to promote dry reforming of methane at low temperature for the direct application to a solid oxide fuel cell'. Together they form a unique fingerprint.

Cite this