Selective conversion of xylose to lactic acid over metal-based Lewis acid supported on γ-Al2O3 catalysts
[Display omitted] •Deposition of Cr, Co, Cu, Ni, or Sn oxides on γ-Al2O3 can promote Lewis acid sites of catalysts.•The acidity of catalyst influences the lactic acid yield.•Oxides of Cr, Co, Cu, Ni, or Sn supported on γ-Al2O3 can induce the D-xylose conversion up to 99%.•Cr/Al2O3 and Sn/Al2O3 are t...
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Published in | Catalysis today Vol. 367; pp. 205 - 212 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.05.2021
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Subjects | |
Online Access | Get full text |
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Summary: | [Display omitted]
•Deposition of Cr, Co, Cu, Ni, or Sn oxides on γ-Al2O3 can promote Lewis acid sites of catalysts.•The acidity of catalyst influences the lactic acid yield.•Oxides of Cr, Co, Cu, Ni, or Sn supported on γ-Al2O3 can induce the D-xylose conversion up to 99%.•Cr/Al2O3 and Sn/Al2O3 are the outstanding catalysts for lactic production with the yield up to 70%.
Gamma-alumina (γ-Al2O3) is a low-cost amphoteric solid catalyst which can enhance the transformation of d-xylose into lactic acid. The deposition of metal oxides on γ-Al2O3 could further improve the yield of lactic acid from xylose. Therefore, in this work, the thermochemical catalytic conversion of d-xylose to lactic acid using the Cr, Cu, Co, Ni, and Sn oxides supported on γ-Al2O3 as heterogeneous catalysts was studied. The effects of metal oxides on the d-xylose conversion to lactic acid activity of the catalysts were investigated. It was found that, under identical testing conditions (170 °C, 4 h), Cr/Al2O3 is superior to the other catalysts with the 99 % conversion of d-xylose and the lactic acid yield of 74%. The outstanding activity could be attributed to its richness in Lewis-acid sites. Since the highly active Cr/Al2O3 catalyst is composed of the earth-abundant materials and can be prepared by a simple process, it has feasibility for industrial-scale application. |
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ISSN: | 0920-5861 1873-4308 |
DOI: | 10.1016/j.cattod.2020.04.061 |