Production of CO-free H2 by formic acid decomposition over Mo2C/carbon catalysts

Ákos Koós, F. Solymosi

Research output: Contribution to journalArticle

38 Citations (Scopus)

Abstract

The vapor phase decomposition of formic acid was studied over supported Mo2C catalysts in a flow system. Mo2C deposited on silica is an effective catalyst for both the dehydrogenation of formic acid to yield H2 and CO2, and its dehydration to yield H2O and CO. The extent of the decomposition approached 100% at 623 K. Preparation of the Mo2C catalyst by the reaction of MoO3 with a multiwall carbon nanotube and carbon Norit, however, dramatically altered the product distribution. Dehydrogenation became the dominant process. In optimum case, the selectivity for H2, expressed in terms of the ratio CO 2/CO + CO2, was 98-99%, even on total conversion at 423-473 K. The addition of water to the formic acid completely eliminated CO formation and furnished CO-free H2 on Mo2C/carbon catalysts at 373-473 K. Another feature of the Mo2C catalyst is its high stability. No changes in activity or selectivity were observed within 10 h. Graphical Abstract: XP spectra of MoO3 in the course of the formation of 1%Mo2C on carbon Norit in the flow of H2 at different temperatures.

Original languageEnglish
Pages (from-to)23-27
Number of pages5
JournalCatalysis Letters
Volume138
Issue number1-2
DOIs
Publication statusPublished - Aug 2010

Fingerprint

formic acid
Formic acid
Carbon Monoxide
Carbon
Decomposition
Catalysts
Dehydrogenation
Charcoal
Dehydration
Catalyst supports
Carbon Nanotubes
Carbon nanotubes
Silicon Dioxide
Vapors
Silica

Keywords

  • Carbon Norit support
  • Formic acid decomposition
  • MoC catalyst
  • Multiwall carbon nanotube support
  • Pure hydrogen production

ASJC Scopus subject areas

  • Catalysis
  • Chemistry(all)

Cite this

Production of CO-free H2 by formic acid decomposition over Mo2C/carbon catalysts. / Koós, Ákos; Solymosi, F.

In: Catalysis Letters, Vol. 138, No. 1-2, 08.2010, p. 23-27.

Research output: Contribution to journalArticle

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