4.8 Article

Improved chemoselective hydrogenation of crotonaldehyde over bimetallic AuAg/SBA-15 catalyst

期刊

JOURNAL OF CATALYSIS
卷 330, 期 -, 页码 135-144

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2015.07.022

关键词

AuAg bimetallic catalyst; Chemoselective hydrogenation; Unsaturated aldehyde; Metal-surface selection rule; FT-IR

资金

  1. National Basic Research Program of China [2011CBA00508]
  2. Natural Science Foundation of China [21173175, 21473145]
  3. Research Fund for the Doctoral Program of Higher Education [20110121130002]
  4. Program for Changjiang Scholars and Innovative Research Team in University [IRT_14R31]
  5. National Research Foundation (NRF), Prime Minister's Office, Singapore, under its Campus for Research Excellence and Technological Enterprise (CREATE) program
  6. Ministry of Education, Singapore [RG129/14]

向作者/读者索取更多资源

Bimetallic AuAg/SBA-15 catalysts were disclosed to efficiently catalyze vapor-phase chemoselective hydrogenation of crotonaldehyde (CRAL) with improved hydrogenation rate and selectivity to crotonyl alcohol (CROL). The CRAL hydrogenation rate and product distribution were remarkably influenced by reaction parameters such as the reaction pressure and CRAL/hydrogen ratio. Ag decoration on Au/SBA-15 effectively stabilized bimetallic AuAg nano-alloy particles in small size and promoted the catalytic stability. In situ FT-IR investigation revealed that unusual C2M2 di-sigma bonded CRAL surface species with reinforced symmetric delta(CH3) IR band under the metal-surface selection rule (MSSR) were formed on bimetallic AuAg/SBA-15. The stronger CRAL chemisorption on bimetallic AuAg/SBA-15 surfaces than on monometallic Au/SBA-15 was possibly due to the relatively strong ligating of C=O bond on Ag active sites and the enhancement of the co-adsorption of the conjugated double bonds of CRAL. Synergistic interaction between Au and Ag active sites for the activation of H-H, C=C and C=O bond may be the origin of positive effect of Ag decoration on Au/SBA-15. (C) 2015 Elsevier Inc. All rights reserved.

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