4.7 Article

Iron-based catalyst (Fe2-xNixTiO5) for tar decomposition in biomass gasification

Journal

FUEL
Volume 300, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.fuel.2021.120859

Keywords

Biomass; Gasification; Tar reforming; Iron catalysis; Ilmenite

Funding

  1. project NOTARGAS [POCI-01-0145-FEDER-030661]
  2. project SusPhotoSolutions -Solucoes Fotovoltaicas Sustentaveis, PO Centro [CENTRO-01-0145-FEDER-000005]
  3. Portuguese Foundation for Science and Technology (FCT)/Ministry of Science, Technology and Higher Education (MCTES) [UIDP/50017/2020 + UIDB/50017/2020, UIDB/50011/2020 & UIDP/50011/2020]
  4. EU Horizon 2020
  5. Portuguese Foundation for Science and Technology
  6. The Navigator Company [PD/BDE/128620/2017, SFRH/BD/129901/2017]
  7. Swedish Gasification Centre (SFC)
  8. Swedish Energy Agency [34721-2]

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The study found that the Fe2-xNixTiO5 catalyst showed high activity in converting model compounds at high temperatures, but the activity decreased with increased time on stream, possibly due to structural changes in iron active phases and sulfur chemisorption on the nickel surface.
In this study, a novel Fe2-xNixTiO5 catalyst for potential applications in biomass gasification gas cleaning/ upgrading was investigated. The material was successfully synthesized through combined mechanical activation and microwave firing. Catalytic steam reforming was studied in a fixed bed tubular reactor, using a mixture of toluene and naphthalene as model tar compounds as well as downstream a fluidized bed gasifier. Fe2-xNixTiO5 catalyst showed high activity in converting the model compounds at temperatures higher than 700 degrees C. The catalyst exhibited a tar conversion of 78% at 800 degrees C when exposed to biomass-derived gas from a bubbling fluidized bed gasifier. Nevertheless, the catalytic activity declined with increased time on stream due to structural changes in iron active phases, caused by redox conditions of the producer gas. Furthermore, thermodynamic calculations suggest that sulfur chemisorption on the nickel surface, may also contribute to the catalyst deactivation.

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