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2020
DOI: 10.1016/j.mcat.2020.111243
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Selective oxidation of glycerol to dihydroxyacetone over N-doped porous carbon stabilized CuxO supported Au catalysts

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Cited by 9 publications
(7 citation statements)
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“…The recyclability of the Au/LPrO catalyst was tested in a recycling experiment for five runs (Figure D). Although the GLY conversion drops from 65.8 to 47.0%, the loss (18.8%) in glycerol conversion is still smaller than those (22–72%) of the previously reported Au/CuO, Au/TiO 2 , Au/SiO 2 , and Au/AC catalysts, indicating the better durability of the Au/LPrO catalyst (Table S7). Besides, ICP analysis proves that almost no detectable Pr element has leached into the reaction solution after catalytic reaction (Table S8), further confirming the high stability of the Au/LPrO catalyst.…”
Section: Results and Discussionmentioning
confidence: 65%
“…The recyclability of the Au/LPrO catalyst was tested in a recycling experiment for five runs (Figure D). Although the GLY conversion drops from 65.8 to 47.0%, the loss (18.8%) in glycerol conversion is still smaller than those (22–72%) of the previously reported Au/CuO, Au/TiO 2 , Au/SiO 2 , and Au/AC catalysts, indicating the better durability of the Au/LPrO catalyst (Table S7). Besides, ICP analysis proves that almost no detectable Pr element has leached into the reaction solution after catalytic reaction (Table S8), further confirming the high stability of the Au/LPrO catalyst.…”
Section: Results and Discussionmentioning
confidence: 65%
“…It is yet difficult to differentiate the Cu + species from Cu 0 by the Cu 2p peak, as they respond at similar binding energies. To determine the valence state of the Cu species, we further analyzed the Auger electron kinetic energy of Cu elements. , In the Auger electron spectrum of CuO-NaOH-R (Figure b), there is a characteristic peak (918.9 eV), the value of which is higher than 918.6 eV (Cu 0 Auger electron kinetic energy), proving the generation of Cu 0 species on the surface of the CuO-NaOH-R sample after the reaction.…”
Section: Resultsmentioning
confidence: 99%
“…Ni@NC catalysts were synthesized based on our previous work. 33,34 Briey, 1.0 g F127 and 2.0 g of dicyandiamide (DCDA) were rst dissolved in a mixture of ethanol (20.0 g) and deionized (DI) water (10.0 g), and then 0.75 g of nickel nitrate hexahydrate and 5.0 g of resol ethanol solution (20 wt%) were added to the above solution. Aer stirring for 0.5 h, the nal solution was put into a drying oven and the solvent was evaporated at 50 C for 6 h, followed by 100 C for 24 h. The obtained composites were calcined in a tubular furnace under N 2 at 350 C for 3 h and then at 600 or 800 C for another 3 h with a heating rate of 3 C min À1 .…”
Section: Catalyst Preparationmentioning
confidence: 99%