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In the current situation of increasing cadmium (Cd) and microplastic composite pollution, Cd adsorption and passivation in various soils by biochar under microplastic co-contamination conditions require further investigation. In this study, the behaviors and mechanisms of KMnO-modified biochar on Cd adsorption and passivation were examined in 50 different soils (5 soil types, 5 Cd concentrations, and 2 microplastic treatments) with the three-layer mesh method. Moreover, acidified biochar was employed to quantify the contributions of mineral and non-mineral mechanisms to Cd adsorption by biochar in soils. The results revealed that microplastics in the soil impeded the biochar remediation of Cd contamination, which was pronounced in more acidic soils. Under biochar treatment, the relatively stable Cd decreased by 2.49 %, 1.97 %, 0.36 %, 0.84 %, and 0.39 % for five soils (from low to high pH) with 5 % microplastics compared to those without microplastics. The Cd adsorption capacity by biochar was higher in soils with lower pH, and microplastic co-contamination further increased Cd adsorption by biochar. Additionally, higher soil pH correlated with a greater contribution of the mineral mechanism to Cd adsorption, and microplastic co-contamination enhanced the contribution of mineral mechanism. This study aimed to gain a deeper understanding of how microplastics in agricultural soils affect the remediation of Cd pollution by biochar. This study highlighted that biochar-based remediation of heavy metal contamination in soils must consider not only soil pH and heavy metal concentrations, but also the effects of co-existing pollutants, such as microplastics.
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http://dx.doi.org/10.1016/j.envres.2025.122476 | DOI Listing |
Water Res
August 2025
State Key Laboratory of Water Pollution Control and Green Resource Recycling, School of Environmental Science and Engineering, Tongji University, 1239 Siping Road, Shanghai 200092, PR China; Shanghai Institute of Pollution Control and Ecological Security, Shanghai 200092, PR China.
A precise modulation of heterogeneous catalysts in structural and surface properties promises the development of more sustainable advanced oxidation water purification technologies. However, the poor catalyst stability due to covering of surface-active sites by oxidation intermediates remains a key bottleneck to their practical applications. Herein we propose a simple defect-induced in-situ single-atom anchoring strategy to overcome this challenge by creating unique asymmetric active-sites on the catalyst surface.
View Article and Find Full Text PDFEnviron Sci Technol
September 2025
Soil and Crop Sciences, School of Integrative Plant Science, College of Agriculture and Life Sciences, Cornell University, Ithaca, New York 14853, United States.
Glyphosate, the most widely used herbicide, undergoes adsorption and abiotic degradation on environmental surfaces, with natural organic matter strongly influencing these processes. The role of organo-mineral associations in regulating glyphosate retention and transformation pathways, however, remains unclear. In this study, we employed time-resolved ATR-FTIR spectroscopy and microfluidic experiments coupled with LC-MS quantification to track glyphosate and its oxidation byproducts.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Key Laboratory of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, P.R. China.
Zinc metal, as the mainstream anode material of aqueous batteries, faces severe side reactions and notorious dendrite growth. Surface passivation of Zn anodes with a protective layer is one of the effective strategies to address these issues. The previous reports have focused on applying different components as surface layers while neglecting the impact of their crystallographic orientation on electrochemical performance.
View Article and Find Full Text PDFRSC Adv
August 2025
Engineering Research Center for Nanomaterials, The First Affiliated Hospital, The Academy for Advanced Interdisciplinary Studies, College of Chemistry and Molecular Sciences, Henan University Zhengzhou 450046 China
Nanoscale zero-valent iron (nZVI) was synthesized by a one-pot liquid-phase chemical method in the presence of FeSO as the iron source and NaBH as the reducing agent. The synthesized nZVI was characterized by scanning electron microscopy, X-ray diffraction, energy dispersive spectrometry, and Fourier transform infrared spectroscopy. Its ability to passivate Pb, Cd, and AsO in soils was evaluated by inductively coupled plasma-atomic emission spectroscopy, and the passivation mechanism was explored based on adsorption thermodynamics and kinetics simulations.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
School of Chemistry and Chemical Engineering, Collaborative Innovation Center of Henan Province for Green Manufacturing of Fine Chemicals, Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, Henan Normal University, Henan, Xinxiang 453007, PR China. Electronic address: zygao
Furfural (FF) is a biomass-derived platform molecule characterized by an aldehyde group attached to a furan ring. The selective electrochemical hydrogenation (ECH) of the aldehyde group into hydroxymethyl offers a sustainable approach for converting FF into valuable furfuryl alcohol (FA) chemical. Efficient catalyst that balances active hydrogen (H*) generation and FF adsorption is crucial for electrochemical FF-to-FA conversion.
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