Effect of amorphous ordered mesoporous carrier on adsorption and desorption of Hg0 over CeOx-amTiO2. (1st June 2023)

• Record Type: Journal Article
• Authors: Li, Bohao; Zhou, Jinsong; Lu, Yang; Zhou, Lingtao; Liu, Zhuang; Zhou, Qixin; Wang, Tang
• Is Part Of: Fuel. Volume 341(2023)
• Publication Date: 2023-06-01
• Subjects: Ordered mesopores -- Amorphous TiO2 -- Hg0 removal -- Wet desorption -- Desorption kinetics; Fuel -- Periodicals; Coal -- Periodicals; Coal; Fuel; Periodicals; 662.6
• DOI: 10.1016/j.fuel.2023.127759
• Languages: English
• ISSNs: 0016-2361

Abstract

Graphical abstract: Highlights: A novel Hg 0 removal adsorbent CeO x -amTiO2 was synthesized via the evaporation-induced self-assembly method. Ordered mesostructures significantly facilitated the adsorption and desorption process. Oxygen vacancies on carriers can reduce the adsorption energy of Hg compounds. The desorption of Hg from adsorbents exhibited biphasic kinetics. Abstract: Improper disposal of deactivated mercury (Hg) adsorbents will cause secondary contamination which is still hazardous to human beings. Wet desorption is a green and environmentally friendly method, but there is a lack of sufficient study. In this work, a cerium oxide loaded ordered mesoporous amorphous titanium dioxide (CeO x -amTiO2 ) composite is obtained based on the evaporation-induced self-assembly (EISA) process. It possesses a high specific surface area (∼198 m 2 /g), uniform pore diameters (∼14.7 nm), and large pore volume (∼0.49 cm 3 /g). The CeO x -amTiO2 demonstrates high adsorption capacity in various atmospheres (63.3 % in pure N2, 95.0 % in N2 + 400 ppm H2 S), and achieves a desorption efficiency of 93.2 % in 0.2 mol/L sodium thiosulfate (Na2 S2 O3 ) solution. The large specific surface area and ordered mesostructure significantly facilitate the mass transfer process, reasonably explaining the strong adsorption capacity and fast desorption kinetics. X-ray photoelectron spectroscopy (XPS) characterization and thermodynamic calculations reveal that the reduction of Ce 3+ plays a key role in the desorption of Hg. In addition, the amorphous carrier structure reduces the binding strength between the adsorption product and the adsorbent, further accelerating the desorption process. This study provides a pathway for the efficient desorption of Hg 0 removal adsorbents.