The leaching of toxic metals is still problematic for heterogeneous metal catalysts in activating peracetic acid (PAA). Herein, CoFe/U-ZrO was synthesized by loading CoFe onto the metal-organic framework (UiO-66) derived ZrO (U-ZrO) for PAA activation. The high porosity and specific surface area of UiO-66 enable efficient embedding and uniform dispersion of CoFe particles into pore channels. The supported material effectively activates PAA and significantly reduces Co leaching. CoFe/U-ZrO-PAA system shows a removal efficiency of sulfamethoxazole reaching 98.9% within 10 min with Co leaching concentrations as low as 0.005 mg/L (equivalent to 1.4% of CoFe-PAA system). Quenching experiments, probe experiments and electron paramagnetic resonance tests identify CHC(O)OO· as the dominant radical species. The CoFe/U-ZrO-PAA system maintains high activity in actual water bodies and can resist the interference of HPO, Cl, SO, NO and humic acid except for the inhibitory effect of HCO. The system also displays good stability and high degradability to different pollutants, maintaining consistently outstanding degradation efficiency in the flow-through experiment. Overall, the environmentally friendly, good efficiency, and high stability of the CoFe/U-ZrO-PAA system makes it potential for broad applications in wastewater treatment.
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http://dx.doi.org/10.1016/j.envres.2025.121329 | DOI Listing |
Environ Res
March 2025
Department of Environmental Engineering, Beijing University of Technology, Beijing 100124, P. R. China; National Engineering Laboratory for Advanced Municipal Wastewater Treatment and Reuse Technology, Beijing University of Technology, Beijing 100124, P. R. China. Electronic address:
The leaching of toxic metals is still problematic for heterogeneous metal catalysts in activating peracetic acid (PAA). Herein, CoFe/U-ZrO was synthesized by loading CoFe onto the metal-organic framework (UiO-66) derived ZrO (U-ZrO) for PAA activation. The high porosity and specific surface area of UiO-66 enable efficient embedding and uniform dispersion of CoFe particles into pore channels.
View Article and Find Full Text PDFJ Colloid Interface Sci
March 2025
State Key Laboratory of Solidification Processing, Center for Nano Energy Materials, School of Materials Science and Engineering, Northwestern Polytechnical University and Shaanxi Joint Lab of Graphene (NPU), No. 127, Youyi West Road, Xi'an 710072, China; New Energy (Photovoltaic) Industry Research Center, Qinghai University, No. 251, Daning Road, Xining 810016, China. Electronic address:
Surface modification of cocatalysts is one of the most efficient strategies to improve the surface charge transfer of bismuth vanadate (BVO) photoanodes. However, the interfacial recombination between BVO semiconductors and cocatalysts is seriously undervalued. Herein, metallic titanium nitride (TiN) nanoparticles are decorated on the surface of BVO to tune the carrier dynamics at BVO/cocatalysts interface.
View Article and Find Full Text PDFJ Colloid Interface Sci
March 2025
Division of Physical Sciences and Engineering, King Abdullah University of Science and Technology, Thuwal 23955-6900, Saudi Arabia. Electronic address:
The conventional preparation of layered double hydroxide (LDH) often limits its catalytic effectiveness in advanced oxidation processes due to agglomeration and inadequate exposure of active sites. In this work, we present a simplified synthesis approach that utilizes zeolitic imidazolate frameworks (ZIF)-67 (Co) as a sacrificial template to in situ fabricate hollow polyhedral CoFe-LDH (HP-LDH), aimed at enhancing the degradation of dye contaminants in aqueous systems. The unique porous and polyhedral structure of HP-LDH, derived from the template, facilitates contact efficiency between the substrate and active metal sites, acting as an effective nanoreactor.
View Article and Find Full Text PDFChemosphere
March 2025
ChemBio Cluster, ITMO University, Lomonosova Street 9, Saint Petersburg, 191002, Russia.
This article has been retracted: please see Elsevier Policy on Article Withdrawal (https://www.elsevier.com/about/policies/article-withdrawal).
View Article and Find Full Text PDFMolecules
February 2025
School of Environmental and Chemical Engineering, Jiangsu University of Science and Technology, Zhenjiang 212100, China.
Electrocatalytic water splitting is a promising approach for obtaining clean hydrogen energy. In this work, novel molybdate@carbon paper composite electrocatalysts (CoxFe10-xMoO@CP), displaying outstanding electrocatalytic capabilities, were deriving from anchoring cobalt/iron molybdate materials onto the surface of carbon paper fibers. By adjusting the cobalt-to-iron ratio, the composite (Co5Fe5MoO@CP), with the optimal molar proportion (Co/Fe = 5/5), exhibited a distinctive nanoflower morphology (50-100 nm), which provided a significant number of active sites for electrocatalytic reactions, and showed the strongest electrocatalytic potency for both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER).
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