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Arsenic sequestration by granular coal gangue functionalized with magnesium: Effects of magnesium and insight of arsenic sorption mechanisms.

Authors :
Chang, Bongsu
Lee, Seon Yong
Kim, Jae-Hyun
Lee, Soonjae
Kim, Bongju
Lee, Young Jae
Source :
Chemosphere. Nov2024, Vol. 367, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

Leveraging natural waste materials for inorganic contaminant removal in solution offers a novel approach to boost resource recycling and foster sustainable development by enhancing waste use. This research advanced the modest arsenite (As[III]) removal capacity of raw coal gangue through a magnesium-soaking and calcination-based surface modification. Batch experiments showed As(III) removal efficiency was improved from 39.8% to 89.9% after modification, independent of initial pH levels. The Langmuir model estimated the maximum sorption capacity of 0.979 mg/g for the modified coal gangue. Physicochemical analyses confirmed that the modification increased the surface area, pore volume and size of the coal gangue. Furthermore, SEM, and subsequent TEM and SAED analyses identified acicular arsenic trioxide (As 2 O 3) on the modified gangue, enhancing As(III) removal. Variations in sorption kinetics hinted at precipitation, likely due to AsO 3 polymer chains formed by As(III)'s sorption onto Mg(OH) 2 , created from MgO hydration in aqueous conditions. Our findings show that coal gangue has potential applications in the development of sustainable methods for waste recycling. [Display omitted] • Granular coal gangue (GCG) can be used as a recycling waste resource for effective As(III) removal. • As(III) removal can be enhanced by surface modification of GCG with Mg sorption and calcination. • Increased sorption sites and facilitated precipitation enhanced As(III) uptake by modified GCG. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00456535
Volume :
367
Database :
Academic Search Index
Journal :
Chemosphere
Publication Type :
Academic Journal
Accession number :
180926696
Full Text :
https://doi.org/10.1016/j.chemosphere.2024.143583