4.6 Article

Enhanced chemoselective hydrogenation of dimethyl oxalate to methyl glycolate over bimetallic Ag-Ni/SBA-15 catalysts

Journal

APPLIED CATALYSIS A-GENERAL
Volume 505, Issue -, Pages 344-353

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.apcata.2015.08.022

Keywords

Silver; Nickel; Hydrogenation; Dimethyl oxalate; Methyl glycolate

Funding

  1. National Basic Research Program of China [2011CBA00508]
  2. Natural Science Foundation of China [21303141, 21403178, 21473145]
  3. Research Fund for the Doctoral Program of Higher Education [20110121130002]
  4. Program for Innovative Research Team in Chinese Universities [IRT_14R31]

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Mesoporous silica SBA-15-supported bimetallic silver-nickel catalysts (Ag-Ni/SBA-15) were prepared by a co-impregnation method for the chemoselective hydrogenation of dimethyl oxalate (DMO) to methyl glycolate (MG). The structure and physicochemical properties of the catalysts were characterized using N-2 adsorption-desorption, X-ray fluorescence spectroscopy, transmission electron microscopy, H-2-temperature-programmed reduction, UV-vis light diffuse reflectance spectroscopy, X-ray photoelectron spectroscopy, fourier-transform infrared spectroscopy and ester temperature-programed desorption. Compared with monometallic Ag or Ni catalyst, the bimetallic Ag-Ni/SBA-15 catalysts exhibited enhanced catalytic performance for the chemoselective hydrogenation of DMO to MG. The optimized Ag-Ni/SBA-15 catalyst with a Ni/Ag atomic ratio of 0.2 presented the highest MG yield and excellent catalytic stability during the hydrogenation of DMO to MG for longer than 140 h. The characterization results suggested that the Ag and Ni bimetallic nanoparticles on the catalyst surfaces likely formed a segregation structure with more Ni species in the core and more Ag in the shell, and electron transfer from Ni to Ag possibly occurred. The interactions between the Ag and Ni species generated more active/adsorption sites and prevented the transmigration of bimetallic nanoparticles during hydrogenation. (C) 2015 Elsevier B.V. All rights reserved.

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