Au/Pt/TiO sub(2) catalysts prepared by redox method for the chemoselective 1,2-propanediol oxidation to lactic acid and an NMR spectroscopy approach for analyzing the product mixture
1,2-propanediol obtained from the waste glycerol is the most prominent substrate to produce lactic acid (LA) through the sustainable "green" catalytic oxidative route. We showed that bimetallic Au/Pt/TiO sub(2) catalysts that could be easily prepared by the redox reaction with preadsorbed...
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Published in | Applied catalysis. A, General Vol. 491; pp. 170 - 183 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
05.02.2015
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Subjects | |
Online Access | Get full text |
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Summary: | 1,2-propanediol obtained from the waste glycerol is the most prominent substrate to produce lactic acid (LA) through the sustainable "green" catalytic oxidative route. We showed that bimetallic Au/Pt/TiO sub(2) catalysts that could be easily prepared by the redox reaction with preadsorbed hydrogen possessed a high activity in the formation of lactic acid from 1,2-propanediol through selective primary hydroxyl group oxidation by an oxygen-air mixture or an air. The most efficient catalyst with the highest TON value was the sample with the lowest Au content. Even the addition of 0.025 wt.% of gold to the 1%Pt/TiO sub(2) catalyst by the redox method resulted in the enhanced 1,2-propanediol conversion up to 96% with the 91% selectivity to LA. The high oxidation activity of the Au/Pt/TiO sub(2) catalysts was ascribed to the strong interaction between the two metals in Au/Pt bimetallic particles and between the bimetallic particles and the support, which was proved by X-ray photoelectron spectroscopy (XPS) analysis, Fourier transform infrared spectroscopy of adsorbed CO (DRIFTS) technique, and temperature programmed reduction method (TPR-H sub(2)). The reaction products were identified and analyzed with the use of 1D and 2D nuclear magnetic resonance spectroscopy (NMR) methods, which also allowed suggesting a plausible up-to-date scheme of 1,2-propanediol catalytic oxidation. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 content type line 23 ObjectType-Feature-2 |
ISSN: | 0926-860X 1873-3875 |
DOI: | 10.1016/j.apcata.2014.11.039 |