Enhancement of photocatalytic oxidation of glucose to value-added chemicals on TiO2 photocatalysts by a zeolite (Type y) support and metal loading

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Abstract

TiO2-based photocatalysts synthesized by the microwave-assisted sol-gel method was tested in the photocatalytic glucose conversion. Modifications of TiO2 with type-Y zeolite (ZeY) and metals (Ag, Cu, and Ag-Cu) were developed for increasing the dispersion of TiO2 nanoparticles and increasing the photocatalytic activity. Effects of the TiO2 dosage to zeolite ratio (i.e., TiO2 /ZeY of 10, 20, 40, and 50 mol %) and the silica to alumina ratio in ZeY (i.e., SiO2:Al2 O3 of 10, 100, and 500) were firstly studied. It was found that the specific surface area of TiO2 /ZeY was 400–590 m2 g−1, which was higher than that of pristine TiO2 (34.38 m2 g−1). The good properties of 20%TiO2 /ZeY photocatalyst, including smaller particles (13.27 nm) and high surface area, could achieve the highest photocatalytic glucose conversion (75%). Yields of gluconic acid, arabinose, xylitol, and formic acid obtained from 20%TiO2 /ZeY were 9%, 26%, 4%, and 35%, respectively. For the effect of the silica to alumina ratio, the highest glucose conversion was obtained from SiO2:Al2 O3 ratio of 100. Interestingly, it was found that the SiO2:Al2 O3 ratio affected the selectivity of carboxylic products (gluconic acid and formic acid). At a low ratio of silica to alumina (SiO2:Al2 O3 = 10), higher selectivity of the carboxylic products (gluconic acid = 29% and formic acid = 32%) was obtained (compared with other higher ratios). TiO2 /ZeY was further loaded by metals using the microwave-assisted incipient wetness impregnation technique. The highest glucose conversion of 96.9 % was obtained from 1 wt. % Ag-TiO2 (40%)/ZeY. Furthermore, the bimetallic Ag-Cu-loaded TiO2 /ZeY presented the highest xylitol yield of 12.93%.

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Roongraung, K., Chuangchote, S., & Laosiripojana, N. (2020). Enhancement of photocatalytic oxidation of glucose to value-added chemicals on TiO2 photocatalysts by a zeolite (Type y) support and metal loading. Catalysts, 10(4). https://doi.org/10.3390/catal10040423

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