Mechanistic investigation on Hg0 capture over MnOx adsorbents: effects of the synthesis methods

This study demonstrated the impacts of the synthesis methods on the textural structures, chemical properties, and Hg 0 capture capability of the MnO x system. Compared with the samples synthesized using the precipitation (PR) and hydrothermal (HT) methods, the adsorbent prepared via the sol-gel (SG)...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of Zhejiang University. A. Science 2023, Vol.24 (1), p.80-90
Hauptverfasser: Ye, Dong, Hu, Yongjin, Jiang, Zhichang, Liu, Xin, Wang, Haining
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:This study demonstrated the impacts of the synthesis methods on the textural structures, chemical properties, and Hg 0 capture capability of the MnO x system. Compared with the samples synthesized using the precipitation (PR) and hydrothermal (HT) methods, the adsorbent prepared via the sol-gel (SG) technique gave the best performance. At 150 °C, ca. 90% Hg 0 removal efficiency was reached after 7.5 h for MnO x prepared by the SG method, ca. 40% higher than that of the other two methods. The specific surface area of the adsorbent synthesized via the SG technique (23 m 2 /g) was almost double that of the adsorbent prepared by the HT method (12 m 2 /g) and three times that of the one prepared by the PR method (7 m 2 /g). The presence of plentiful acid sites from the SG method facilitated the physisorption of Hg 0 , making more Hg 0 available to be oxidized to HgO by the redox sites and thus giving the adsorbent prepared by the SG method the highest Hg 0 removal efficiency. The strong oxidative ability accelerated the oxidation of the physically adsorbed Hg 0 to HgO, which explained the higher Hg 0 removal efficiency of the sample prepared using the HT method than that of the one synthesized by the PR technique. During the whole Hg 0 removal cycles, chemisorption dominated, with the initial adsorption stage and the external mass-transfer process playing important roles.
ISSN:1673-565X
1862-1775
DOI:10.1631/jzus.A2200388