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A non-syn-gas catalytic route to methanol production

Author

Listed:
  • Cheng-Tar Wu

    (Wolfson Catalysis Centre, University of Oxford)

  • Kai Man Kerry Yu

    (Wolfson Catalysis Centre, University of Oxford)

  • Fenglin Liao

    (Wolfson Catalysis Centre, University of Oxford)

  • Neil Young

    (University of Oxford)

  • Peter Nellist

    (University of Oxford)

  • Andrew Dent

    (Diamond Light Source Ltd, Harwell Science and Innovation Campus)

  • Anna Kroner

    (Diamond Light Source Ltd, Harwell Science and Innovation Campus)

  • Shik Chi Edman Tsang

    (Wolfson Catalysis Centre, University of Oxford)

Abstract

Methanol is an important platform molecule for chemical synthesis and its high energy density also renders it a good candidate as a cleaner transportation fuel. At present, methanol is manufactured from natural gas via the indirect syn-gas route. Here we show that ethylene glycol, a versatile chemical derived from biomass or fossil fuels, can be directly converted to methanol in hydrogen with high selectivity over a Pd/Fe2O3 co-precipitated catalyst. This opens up a possibility for diversification in natural resources for energy-starved countries. The working catalyst contains extremely small 'PdFe' clusters and metal adatoms on defective iron oxide to give the required metal-support interaction for the novel synthesis.

Suggested Citation

  • Cheng-Tar Wu & Kai Man Kerry Yu & Fenglin Liao & Neil Young & Peter Nellist & Andrew Dent & Anna Kroner & Shik Chi Edman Tsang, 2012. "A non-syn-gas catalytic route to methanol production," Nature Communications, Nature, vol. 3(1), pages 1-8, January.
  • Handle: RePEc:nat:natcom:v:3:y:2012:i:1:d:10.1038_ncomms2053
    DOI: 10.1038/ncomms2053
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    Cited by:

    1. Jianghao Zhang & Wenda Hu & Binbin Qian & Houqian Li & Berlin Sudduth & Mark Engelhard & Lian Zhang & Jianzhi Hu & Junming Sun & Changbin Zhang & Hong He & Yong Wang, 2023. "Tuning hydrogenation chemistry of Pd-based heterogeneous catalysts by introducing homogeneous-like ligands," Nature Communications, Nature, vol. 14(1), pages 1-10, December.

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