4.7 Article

Highly selective hydrogenation of furfural to tetrahydrofurfuryl alcohol over MIL-101(Cr)-NH2 supported Pd catalyst at low temperature

Journal

CHINESE JOURNAL OF CATALYSIS
Volume 39, Issue 2, Pages 319-326

Publisher

SCIENCE PRESS
DOI: 10.1016/S1872-2067(18)63009-8

Keywords

Metal-organic frameworks; Amino functionalization; Pd nanoparticle; Biomass; Selective hydrogenation

Funding

  1. National Natural Science Foundation of China [21573031, 21673032]
  2. Program for Excellent Talents in Dalian City [2016RD09]
  3. Fundamental Research Funds for the Central Universities [DUT17LK21]
  4. State Key Laboratory of Physical Chemistry of Solid Surfaces, Xiamen University [201507]

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An efficient heterogeneous catalyst Pd@MIL-101(Cr)-NH2, is prepared through a direct pathway of anionic exchange followed by hydrogen reduction with amino-containing MIL-101 as the host matrix. The composite is thermally stable up to 350 degrees C and the Pd nanoparticles uniformly disperse on the matal organic framework (MOF) support, which are attributed to the presence of the amino groups in the frameworks of MIL-101(Cr)-NH2. The selective hydrogenation of biomass-based furfural to tetrahydrofurfuryl alcohol is investigated by using this multifunctional catalyst Pd@MIL-101(Cr)-NH2 in water media. A complete hydrogenation of furfural is achieved at a low temperature of 40 degrees C with the selectivity of tetrahydrofurfuryl alcohol close to 100%. The amine-functionalized MOF improves the hydrogen bonding interactions between the intermediate furfuryl alcohol and the support which is conducive for the further hydrogenation of furfuryl alcohol to tetrahydrofurfuryl alcohol in good coordination with the metal sites. (C) 2018, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.

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