4.7 Article

Competition between acidic sites and hydrogenation sites in Cu/ZrO2 catalysts with different crystal phases for conversion of biomass-derived organics

期刊

GREEN ENERGY & ENVIRONMENT
卷 6, 期 4, 页码 557-566

出版社

KEAI PUBLISHING LTD
DOI: 10.1016/j.gee.2020.05.007

关键词

Zirconia supported copper catalyst; Crystal phase; Hydrogenation; Hydrogenation sites; Acidic sites

资金

  1. National Natural Science Foundation of China [51876080]
  2. Program for Taishan Scholars of Shandong Province Government

向作者/读者索取更多资源

The crystal phases of zirconium oxides can influence the distribution of catalytic sites and impact the conversion of organics like furfural and vanillin in hydrogenation reactions. Monoclinic zirconia supported copper catalyst exhibits higher hydrogenation activity in furfural hydrogenation, while tetragonal zirconia supported copper catalyst is more suitable for acid-catalyzed reactions.
Oxides with different crystal phases can have important effects on the configuration of surface atoms, which can further affect the distribution of hydrogenation sites and acidic sites as well as the competitions of these varied types of catalytic sites. This could be potentially used to tailor the distribution of the products. In this study, zirconium oxides with different crystal phases supported copper catalysts were prepared for the hydrogenation of the biomass-derived furfural, vanillin, etc. The results showed that both calcination temperature and Cu species affected the shift of zirconia from tetragonal phase to the monoclinic phase. Monoclinic zirconia supported copper catalyst can effectively catalyze the hydrogenation of furfural to furfuryl alcohol via hydrogenation route due to its low amount of Bronsted acidic sites, although the surface area and the exposed metallic Cu surface area were much lower than the tetragonal zirconia supported copper catalyst. Zirconia with tetragonal or tetragonal/monoclinic phases supported copper catalysts contain abundant acidic sites and especially the Bronsted acidic sites, which catalyzed mainly the conversion of furfural via the acid-catalyzed routes such as the acetalization, rather than the hydrogenation. The acidic sites over the Cu/ZrO2 catalyst played more predominant roles than the hydrogenation sites in determining the conversion of the organics like furfural and vanillin. (C) 2020, Institute of Process Engineering, Chinese Academy of Sciences. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd.

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