S-scheme heterojunction CeO2/TiO2 modified by reduced graphene oxide (rGO) as charge transfer route for integrated photothermal catalytic oxidation of Hg0

[Display omitted] •rGO modified CeO2/TiO2 was synthesized and explored the removal efficiency of Hg0.•The photothermal catalytic oxidation of Hg0 was dominated by physical adsorption.•S-scheme heterojunction rGO/CeO2/TiO2 performed high redox ability.•The Hg0 oxidation efficiency of 5GCT was 1.5 tim...

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Veröffentlicht in:Fuel (Guildford) 2023-07, Vol.343, p.127973, Article 127973
Hauptverfasser: Zheng, Ji-Ren, Yuan, Chung-Shin, Ie, Iau-Ren, Shen, Huazhen
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Sprache:eng
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Zusammenfassung:[Display omitted] •rGO modified CeO2/TiO2 was synthesized and explored the removal efficiency of Hg0.•The photothermal catalytic oxidation of Hg0 was dominated by physical adsorption.•S-scheme heterojunction rGO/CeO2/TiO2 performed high redox ability.•The Hg0 oxidation efficiency of 5GCT was 1.5 times higher than CeO2/TiO2 at 200 °C. This study explored the photothermal catalytic oxidation of Hg0 by using S-scheme heterojunction CeO2/TiO2 modified by reduced graphene oxide (rGO) at 100-200 °C. The surface properties of self-prepared photothermal catalysts were characterized by BET, SEM, TEM, EDS, XRD, Raman, UV–Vis, XPS, EPR, and UPS. The crystal structure of TiO2 was mainly anatase and the nano-sized CeO2/TiO2 was uniformly distributed on the surface of the rGO sheet. The oxidation efficiency of Hg0 decreased with reaction temperature in the order of Ƞ100 °C = Ƞ150 °C > Ƞ200 °C, implying that the oxidation of Hg0 was controlled by mass transfer governed by adsorption instead of photothermal catalytic reaction. Both photo- and thermos-catalytic reaction mechanisms were involved in the oxidation of Hg0 at 100–200 °C. Moreover, rGO-modified CeO2/TiO2 could tolerate multi-pollutants (SO2 and NO) except for 100 ppm NO, which slightly reduced the oxidation efficiency of Hg0.
ISSN:0016-2361
1873-7153
DOI:10.1016/j.fuel.2023.127973