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Fischer-tropsch synthesis: Preconditioning effects upon co-containing promoted and unpromoted catalysts

  • Donald C. Cronauer
  • , Jeffrey W. Elam
  • , A. Jeremy Kropf
  • , Christopher L. Marshall
  • , Pei Gao
  • , Shelley Hopps
  • , Gary Jacobs
  • , Burtron H. Davis

Producción científica: Articlerevisión exhaustiva

13 Citas (Scopus)

Resumen

In the preparation and evaluation of Fischer- Tropsch (FT) catalysts, active catalysts formed by both incipient wetness impregnation (IWI) and atomic layer deposition (ALD) of major components were demonstrated. ALD-deposited Co on a silica support was more effective than a similar catalyst deposited upon a support of ALD-deposited Al 2O 3 on silica. The addition of Co reduction promoters including Pt, Ir and Ru using either ALD or IWI has been shown to strongly affect the catalyst pre-conditioning step. CO conversion results were consistent with previously reported Temperature Programmed Reduction X-ray Absorption Near-edge Structure/Extended X-ray Absorption Fine Structure Spectroscopy (TPRXANES/ EXAFS) experiments observing the nature of chemical transformations occurring during the activation of cobalt-based FT catalysts in hydrogen. Specifically, there exists a 2-step reduction process involving Co 3O 4 to Co O and Co O to Co 0 transformations. The extent of catalyst preconditioning was strongly affected by the reduction temperature (with 400 °C preferred) and the loading of the promoter. This was demonstrated using a continuous-flow catalytic-bed unit with a 2:1 molar blend of H2:CO, at temperatures ranging from about 260 to 300 °C, pressures averaging 1.3 MPa (190 psia), and gas space velocities about 24 NL/h-g.

Idioma originalEnglish
Páginas (desde-hasta)698-713
Número de páginas16
PublicaciónCatalysis Letters
Volumen142
N.º6
DOI
EstadoPublished - jun 2012

Financiación

Acknowledgments The work carried out at the CAER was supported in part by funding from a grant from NASA (#NNX07AB93A), as well as the Commonwealth of Kentucky. Argonne’s research was supported in part by the U.S. Department of Energy (DOE), Office of Fossil Energy, National Energy Technology Laboratory (NETL) under Project AA-10-15; 49261-00-107. The use of the Advanced Photon Source was supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, under Contract DE-AC02-06CH11357. MRCAT operations are supported by the Department of Energy and the MRCAT member institutions. J.W. Elam was supported as part of the Institute for Atom-efficient Chemical Transformations (IACT), an Energy Frontier Research Center funded by the U.S. Department of Energy (DOE), Office of Science, Office of Basic Energy Science. The SEM scans were prepared by D.J. Schroeder and A. Hubaud using a FEI Quanta 400F ESEM unit. The electron microscopy was accomplished at the Electron Microscopy Center for Materials Research at Argonne National Laboratory, a U.S. Department of Energy Office of Science Laboratory operated under Contract No. DE-AC02-06CH11357 by UChicago Argonne, LLC.

FinanciadoresNúmero del financiador
Basic Energy Sciences Office of Science
Office of Basic Energy SciencesDE-AC02-06CH11357
U.S. Department of Energy Office of Science Laboratory
U.S. Department of Energy EPSCoR
National Aeronautics and Space Administration07AB93A
Office of Fossil Energy and Carbon Management
Office of Science Programs
Argonne National Laboratory
National Energy Technology LaboratoryAA-10-15, 49261-00-107

    ASJC Scopus subject areas

    • Catalysis
    • General Chemistry

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