Benzene derivatives in wastewater have negative impacts on ecosystems and human health, making their removal prior to discharge imperative. In this study, FeO@AC-NH@Cu-opa (AC-NH = aminoclay, Cu-opa = [Cu(opa)(bipy)(HO)] (Hopa = 3-(4-oxypyridinium-1-yl) phthalic acid)) nanoparticles (NPs) were synthesized as adsorbent and catalyst for phenolic compound removal from wastewater. FeO@AC-NH@Cu-opa NPs demonstrated outstanding performance in the adsorption of phenol, exhibiting a remarkable adsorption capacity of up to 166.39 mg g according to the Langmuir model. The composite also exhibited higher Fenton activity toward the degradation of electron-rich organic phenolic pollutants, with a rate approximately 3.4 times higher than that of FeO alone. The high catalytic activity of the composite was attributed to the large surface area and abundant active sites of the 2D charge-separated Cu-MOF. Meanwhile, the superparamagnetism of the FeO core enabled magnetic recollection and reuse without any significant loss of activity. Therefore, use of FeO@AC-NH@Cu-opa/HO shows potential in an efficient method for the removal of phenolic compounds from wastewater.
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http://dx.doi.org/10.1039/d3dt03431c | DOI Listing |
Environ Pollut
December 2024
School of Environmental Science and Engineering, Zhejiang Gongshang University, Hangzhou, 310018, China. Electronic address:
J Hazard Mater
December 2024
Key Laboratory of Eco-Environments in Three Gorges Reservoir Region, Ministry of Education, College of Environment and Ecology, Chongqing University, Chongqing 400045, PR China.
Carbonate radical (CO) is inevitably produced in advanced oxidation processes (AOPs) when addressing real-world aqueous environments, yet it often goes unnoticed due to its relatively lower reactivity. In this study, we emphasized the pivotal role of CO in targeting the elimination of contaminants by contrasting it with conventional reactive oxygen species (ROSs) and assessing the removal of sulfamethazine (SMT). Similar to singlet oxygen (O), CO shows a preference for electron-rich organic compounds.
View Article and Find Full Text PDFWater Res
December 2024
State Key Laboratory of Urban Water Resource and Environment, School of Environment, Harbin Institute of Technology, Harbin, 150090, China. Electronic address:
The integration of membrane separation with heterogeneous advanced oxidation processes is a prospective strategy for the elimination of contaminants during wastewater treatment. Fe-based catalysts and the green oxidant peracetic acid (PAA) are desirable candidates for the development of catalytic membranes because they are environmentally friendly. However, the construction of catalytic ceramic membranes (CMs) modified with efficient Fe-based catalysts that generate increased amounts of high-valent Fe-O species during PAA activation for the degradation of specific pollutants, especially during instantaneous membrane filtration, remains challenging.
View Article and Find Full Text PDFSci Bull (Beijing)
December 2024
Key Lab for Special Functional Materials of Ministry of Education, National & Local Joint Engineering Research Center for High-efficiency Display and Lighting Technology, School of Nanoscience and Materials Engineering, and Collaborative Innovation Center of Nano Functional Materials and Applications, Henan University, Kaifeng 475004, China. Electronic address:
Mixed Sn-Pb perovskites are attracting significant attention due to their narrow bandgap and consequent potential for all-perovskite tandem solar cells. However, the conventional hole transport materials can lead to band misalignment or induce degradation at the buried interface of perovskite. Here we designed a self-assembled material 4-(9H-carbozol-9-yl)phenylboronic acid (4PBA) for the surface modification of the substrate as the hole-selective contact.
View Article and Find Full Text PDFJ Hazard Mater
December 2024
School of Environmental and Municipal Engineering, Xi'an University of Architecture and Technology, No.13, Yanta Road, Beilin District, Xi'an 710055, Shaanxi, PR China.
Combining chemical oxidation and adsorption is highly desirable but challenging to remove organoarsenic compounds for water purification. Herein, we prepared a Zn-doped CuO (CuZnO-2) catalyst by incorporating Zn atoms into the CuO lattice, which results in abundant surface oxygen vacancies (OVs) and modulates the electronic structure of Cu-OVs-Zn sites for PMS activation to degrade p-arsanilic acid (p-ASA) and adsorb the secondary arsenic species simultaneously. The elevated d-band centers for Cu upward to the Fermi level can significantly strengthen the adsorption of PMS, p-ASA, and the generated arsenic species.
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