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  Different routes to methanol: inelastic neutron scattering spectroscopy of adsorbates on supported copper catalysts

Kandemir, T., Friedrich, M., Parker, S. F., Studt, F., Lennon, D., Schlögl, R., et al. (2016). Different routes to methanol: inelastic neutron scattering spectroscopy of adsorbates on supported copper catalysts. Physical Chemistry Chemical Physics, 18(26), 17253-17258. doi:10.1039/c6cp00967k.

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 Creators:
Kandemir, Timur1, Author           
Friedrich, Matthias1, Author           
Parker, Stewart F. 2, Author
Studt, Felix 3, Author
Lennon, David 4, Author
Schlögl, Robert1, Author           
Behrens, Malte 5, Author
Affiliations:
1Inorganic Chemistry, Fritz Haber Institute, Max Planck Society, ou_24023              
2ISIS Facility, STFC Rutherford Appleton Laboratory, Chilton, Didcot, Oxfordshire, OX11 0QX, UK, ou_persistent22              
3SUNCAT Center for Interface Science and Catalysis, SLAC National Accelerator Laboratory, 2575 Sand Hill Road, Menlo Park, CA 94025, USA, ou_persistent22              
4School of Chemistry, Joseph Black Building, University of Glasgow, Glasgow, G12 8QQ, UK, ou_persistent22              
5Faculty of Chemistry and CENIDE, University of Duisburg-Essen, Universitätsstr. 7, 45141 Essen, Germany, ou_persistent22              

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 Abstract: We have investigated methanol synthesis with model supported copper catalysts, Cu/ZnO and Cu/MgO, using CO/H2 and CO2/H2 as feedstocks. Under CO/H2 both catalysts show chemisorbed methoxy as a stable intermediate, the Cu/MgO catalyst also shows hydroxyls on the support. Under CO2/H2 the catalysts behave differently, in that formate is also seen on the catalyst. For the Cu/ZnO catalyst hydroxyls are present on the metal whereas for the Cu/MgO hydroxyls are found on the support. These results are consistent with a recently published model for methanol synthesis and highlight the key role of ZnO in the process.

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 Dates: 2016-02-122016-04-052016-04-142016-07-14
 Publication Status: Issued
 Pages: 6
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1039/c6cp00967k
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Title: Physical Chemistry Chemical Physics
  Abbreviation : Phys. Chem. Chem. Phys.
Source Genre: Journal
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Publ. Info: Cambridge, England : Royal Society of Chemistry
Pages: 6 Volume / Issue: 18 (26) Sequence Number: - Start / End Page: 17253 - 17258 Identifier: ISSN: 1463-9076
CoNE: https://pure.mpg.de/cone/journals/resource/954925272413_1