4.8 Article

Selective production of arenes via direct lignin upgrading over a niobium-based catalyst

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NATURE COMMUNICATIONS
卷 8, 期 -, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/ncomms16104

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资金

  1. National Natural Science Foundation of China [91545103, 21603072, 21403065]
  2. Science and Technology Commission of Shanghai Municipality [10dz2220500]
  3. Fundamental Research Funds for the Central Universities [222201718003]
  4. University of Manchester
  5. EPSRC in the United Kingdom [EP/P011632/1]
  6. Scientific User Facilities Division, Office of Basic Energy Sciences, US Department of Energy
  7. Laboratory Directed Research and Development program at the Oak Ridge National Laboratory
  8. Engineering and Physical Sciences Research Council [EP/P011632/1] Funding Source: researchfish
  9. EPSRC [EP/P011632/1] Funding Source: UKRI

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Lignin is the only large-volume renewable source of aromatic chemicals. Efficient depolymerization and deoxygenation of lignin while retaining the aromatic functionality are attractive but extremely challenging. Here we report the selective production of arenes via direct hydrodeoxygenation of organosolv lignin over a porous Ru/Nb2O5 catalyst that enabled the complete removal of the oxygen content from lignin. The conversion of birch lignin to monomer C-7-C-9 hydrocarbons is nearly quantitative based on its monomer content, with a total mass yield of 35.5 wt% and an exceptional arene selectivity of 71 wt%. Inelastic neutron scattering and DFT calculations confirm that the Nb2O5 support is catalytically unique compared with other traditional oxide supports, and the disassociation energy of C-aromatic-OH bonds in phenolics is significantly reduced upon adsorption on Nb2O5, resulting in its distinct selectivity to arenes. This one-pot process provides a promising approach for improved lignin valorization with general applicability.

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