A crucial role of O2− and O22− on mayenite structure for biomass tar steam reforming over Ni/Ca12Al14O33

Newly synthesized nickel calcium aluminum catalysts (Ni/Ca12Al14O33) were tested in a fixed bed reactor for biomass tar steam reforming, toluene as tar destruction model compound. Four catalysts (Ni/Ca12Al14O33) were prepared with Ni loading amount from 1, 3, 5 to 7wt%, even 1% loading catalyst also...

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Published inApplied catalysis. B, Environmental Vol. 88; no. 3-4; pp. 351 - 360
Main Authors Li, Chunshan, Hirabayashi, Daisuke, Suzuki, Kenzi
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier B.V 01.05.2009
Elsevier
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Summary:Newly synthesized nickel calcium aluminum catalysts (Ni/Ca12Al14O33) were tested in a fixed bed reactor for biomass tar steam reforming, toluene as tar destruction model compound. Four catalysts (Ni/Ca12Al14O33) were prepared with Ni loading amount from 1, 3, 5 to 7wt%, even 1% loading catalyst also showed excellent performance. Catalysts aged experiments in the absence (60h on stream) and presence of H2S were characterized by BET, X-ray diffraction (XRD), and Raman spectra. It was observed that Ni/Ca12Al14O33 showed excellent sustainability against coke formation due to the “free oxygen” in the catalysts. It also exhibited higher H2S-poisoning resistance property compared to the commercial catalysts Ni/Al2O3 (5%) and Ni/CaO0.5/MgO0.5. Raman spectra revealed that “free oxygen O2− and O22−” in the structure of the catalysts could be substituted by sulfur then protected Ni poisoning on some degree, but reactivation experiments by O2 flowing showed that the sulfide Ni/Ca12Al14O33 was difficult to completely restore, incorporation of sulfur in the structure only partly regain by O2. The kinetic model proposes, as generally accepted, a first-order reaction for toluene with activation energy of 82.06kJmol−1 was coincident with the literature data. The Ni/Ca12Al14O33 catalyst was effective and relative cheap, which may be lead to reduction in the cost of hot gas cleaning process.
ISSN:0926-3373
1873-3883
DOI:10.1016/j.apcatb.2008.11.004