Fe and N co-doped walnut shell biochar (Fe,N-BC) was prepared through a one-pot pyrolysis procedure by using walnut shells as feedstocks, melamine as the N source, and iron (III) chloride as the Fe source. Moreover, pristine biochar (BC), nitrogen-doped biochar (N-BC), and α-FeO-BC were synthesized as controls. All the prepared materials were characterized by different techniques and were used for the activation of peroxymonosulfate (PMS) for the degradation of sulfamethoxazole (SMX). A very high degradation rate for SMX (10 mg/L) was achieved with Fe,N-BC/PMS (0.5 min), which was higher than those for BC/PMS (0.026 min), N-BC/PMS (0.038 min), and α-FeO-BC/PMS (0.33 min) under the same conditions. This is mainly due to the formation of FeC and iron oxides, which are very reactive for the activation of PMS. In the next step, Fe,N-BC was employed for the formation of a composite membrane structure by a liquid-induced phase inversion process. The synthesized ultrafiltration membrane not only exhibited high separation performance for humic acid sodium salt (HA, 98%) but also exhibited improved self-cleaning properties when applied for rhodamine B (RhB) filtration combined with a PMS solution cleaning procedure. Scavenging experiments revealed that O was the predominant species responsible for the degradation of SMX. The transformation products of SMX and possible degradation pathways were also identified. Furthermore, the toxicity assessment revealed that the overall toxicity of the intermediate was lower than that of SMX.
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http://dx.doi.org/10.1016/j.envpol.2024.124018 | DOI Listing |
Environ Sci Pollut Res Int
January 2025
Centre de Recherche Scientifique Et Technique en Analyses Physico-Chimiques, CP 42004, Bou-Ismail, Tipaza, Algeria.
ZnO-CoO material was successfully synthesized by the co-precipitation method and used as a catalyst for the removal of diclofenac sodium (DCF). ZnO-CoO exhibited higher catalytic activity in the catalytic process compared to the photocatalytic processes. Under optimum conditions, the activation of peroxymonosulfate (PMS) by ZnO-CoO achieved approximately 99% removal of DCF, confirming the effective adsorption and activation of PMS.
View Article and Find Full Text PDFNat Commun
January 2025
School of Chemical Engineering, The University of Adelaide, Adelaide, SA, Australia.
High-entropy alloy nanoparticles (HEA-NPs) exhibit favorable properties in catalytic processes, as their multi-metallic sites ensure both high intrinsic activity and atomic efficiency. However, controlled synthesis of uniform multi-metallic ensembles at the atomic level remains challenging. This study successfully loads HEA-NPs onto a nitrogen-doped carbon carrier (HEAs) and pioneers the application in peroxymonosulfate (PMS) activation to drive Fenton-like oxidation.
View Article and Find Full Text PDFNat Commun
January 2025
CAS Key Laboratory of Urban Pollutant Conversion, Department of Environmental Science and Engineering, University of Science and Technology of China, Hefei, 230026, China.
Single-atom catalysts (SACs) have been increasingly acknowledged for their performance in sustainable Fenton-like catalysis. However, SACs face a trade-off between activity and stability in peroxymonosulfate (PMS)-based systems. Herein, we design a nano-island encapsulated single cobalt atom (Co-ZnO) catalyst to enhance the activity and stability of PMS activation for contaminant degradation via an "island-sea" synergistic effect.
View Article and Find Full Text PDFEnviron Pollut
December 2024
School of Environmental Science and Engineering, Zhejiang Gongshang University, Hangzhou, 310018, China. Electronic address:
Environ Res
December 2024
School of Environment and Architecture, University of Shanghai for Science and Technology, 516 Jungong Rd., Shanghai, 200093, PR China. Electronic address:
The technology to solve the problem of the efficient pollutant removal in peroxymonosulfate (PMS) activation was the ultimate goal. There was an urgent need to achieving higher catalytic activity and oxidation efficiency. Herein, we present a MgAl-based layered double hydroxide assembled as a 2D confined catalyst (MgAl-Co-LDH) with Co metal in chelated form (Co-EDTA) for highly efficient PMS activation degrading sulfamethoxazole (SMX).
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