4.7 Article

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

期刊

CHINESE JOURNAL OF CATALYSIS
卷 39, 期 2, 页码 319-326

出版社

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

关键词

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

资金

  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]

向作者/读者索取更多资源

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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