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Degradation of organic pollutants through activating bisulfite with lanthanum ferrite-loaded biomass carbon.

Authors :
Meng X
Li Y
Liu Y
Zhou R
Fu Y
Chen J
Source :
RSC advances [RSC Adv] 2023 Aug 21; Vol. 13 (35), pp. 24819-24829. Date of Electronic Publication: 2023 Aug 21 (Print Publication: 2023).
Publication Year :
2023

Abstract

The removal of methylene blue (MB) in water is a challenging task due to its toxicity, carcinogenicity and resistance to biodegradation. Accordingly, a novel composite catalyst (BC@LF) was prepared by loading lanthanum ferrite (LaFeO <subscript>3</subscript> ) on biomass carbon (BC) to activate bisulfite (BS) for methylene MB removal in this study. Characterization via scanning electron microscopy (SEM), X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR) indicated that LaFeO <subscript>3</subscript> was successfully loaded on BC. X-ray photoelectron spectroscopy (XPS) analysis suggested that [triple bond, length as m-dash]Fe(iii) was the main active site for BS activation. It was found that 99.4% MB was removed within 60 min in BC@LF/BS system. Sulfate radical (SO <subscript>4</subscript> ˙ <superscript>-</superscript> ) and hydroxyl radicals (HO˙) were proved to be responsible for MB removal in the BC@LF/BS system and SO <subscript>5</subscript> ˙ <superscript>-</superscript> might also be involved in MB removal. The degradation efficiency of MB in the BC@LF/BS system decreased with increasing pH, while the adsorption efficiency of BC@LF for MB improved with increasing pH. Additionally, BC@LF exhibited good reusability for BS activation in successive uses. The BC@LF/BS system exhibited favorable removal effect for various organic compounds, indicating that it has good applicability in the treatment of organic wastewater.<br />Competing Interests: There are no conflicts to declare.<br /> (This journal is © The Royal Society of Chemistry.)

Details

Language :
English
ISSN :
2046-2069
Volume :
13
Issue :
35
Database :
MEDLINE
Journal :
RSC advances
Publication Type :
Academic Journal
Accession number :
37608974
Full Text :
https://doi.org/10.1039/d3ra04271e