Solar zerovalent iron (ZVI) was studied at circumneutral pH in combination with hydrogen peroxide and persulfate for removal of imidacloprid as a model contaminant in natural water. Three commercial ZVI sources, steel wool (ZVI-SW) and two iron micro-powders (ZVI-MS and ZVI-S) were independently evaluated. First, different ZVI corrosion conditions were tested in contact with air, exposed to natural solar radiation and with addition of oxidants, such as HO and SO, demonstrating the importance of released iron. Then, the technical feasibilities of solar/HO/ZVI and solar/SO/ZVI were assessed for the elimination of 1 mg/L of imidacloprid. In general, HO concentrations and treatment times were high. Only ZVI-MS (1 mM) reached 80% imidacloprid degradation after 157 min and 3 mM (102 mg/L) of HO. Solar/SO/ZVI performance was better, reaching >80% imidacloprid degradation in <60 min with 1 mM (192 mg/L) SO for all ZVI sources. Efficiency was highest with ZVI-MS, which was therefore selected for feasibility testing of a microcontaminant (MC) mixture containing 100 μg/L each of atrazine, carbendazim, imidacloprid and thiamethoxam with both solar/oxidizing agents/ZVI. HO took 180 min to achieve 76% degradation of the sum of MCs, while 80% total degradation was reached after 69 min by adding SO, confirming its higher efficiency. Finally, this study showed that ZVI in combination with solar radiation does not enhance significantly the photocatalytic cycle.
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http://dx.doi.org/10.1016/j.chemosphere.2021.131557 | DOI Listing |
Sci Total Environ
January 2025
Institute of Microbiology of the National Academy of Sciences of Belarus, Acad. Kuprevich str., 2, 220084 Minsk, Belarus.
There is an urgent need to develop effective and sustainable methods to decrease sulfonamide (SA) contamination of soil. Herein, a non-homogeneous system of zero-valent metal-biochar-based composites was proposed and tested for persulfate (PS) activation. This system employed zero-valent iron (Fe) as an electron donor to catalyze the cleavage of the OO bond in PS, thereby generating reactive oxygen species (ROS) that degrade SAs.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240, China.
Defluorination reactions are increasingly vital due to the extensive use of organofluorine compounds with robust carbon-fluorine (C-F) bonds; particularly, the efficient defluorination of widespread and persistent per- and polyfluoroalkyl substances under mild conditions is crucial due to their accumulation in the environment and human body. Herein, we demonstrate that surface-modified silicate of pronounced proton affinity can confine active hydrogen (•H) onto nanoscale zerovalent iron (nZVI) by withdrawing electrons from nZVI to react with bound protons, generating confined active hydrogen (•H) for efficient defluorination under ambient conditions. The exposed silicon cation (Si) of silicate functions as a Lewis acid site to activate the C-F bond by forming Si.
View Article and Find Full Text PDFHeliyon
January 2025
Department of Pharmaceutical Science, Faculty of Pharmacy, Umm Al-Qura University, Makkah, P.O. Box 751, Saudi Arabia.
This study presents the synthesis and application of water-ball (sodium polyacrylate) stabilized zero-valent iron nanoparticles (wb@Fe) for the eco-friendly degradation of Methyl Orange (MO). The nanoparticles were prepared using a chemical reduction method using NaBH. Characterization techniques including Field Emission Scanning Electron Microscopy (FESEM), Energy Dispersive X-ray Spectroscopy (EDS), Fourier Transform Infrared Spectroscopy (FTIR), X-ray Photoelectron Spectroscopy (XPS), and X-ray Diffraction (XRD) were employed to analyze the morphology, elemental composition, valent state and crystallinity of the nanoparticles.
View Article and Find Full Text PDFEnviron Res
January 2025
Key Laboratory of the Three Gorges Reservoir Region's Eco-Environment, Ministry of Education, Chongqing University, Chongqing, 400045, China. Electronic address:
Residual antibiotics in aquatic environments pose health and ecological risks due to their persistence and resistance to biodegradation. Thus, it is crucial to develop efficient technologies for the degradation of such antibiotics. This study presents a novel approach using a nano zero-valent iron/graphitic carbon nitride (nZVI/g-CN)-enhanced dielectric barrier discharge (DBD) plasma process for the degradation of ciprofloxacin (CIP).
View Article and Find Full Text PDFMolecules
December 2024
School of Life Science, Shanxi University, Taiyuan 030006, China.
Malic acid-derived polyamides, polyhydrazides, and hydrazides exhibit strong potential for a variety of biological applications. This study demonstrates the synthesis of cobalt, silver, copper, zinc, and iron particles by a facile chemical reduction approach utilizing malic acid-derived polyamides, polyhydrazides, and hydrazides as stabilizing and reducing agents. Comprehensive characterization of the particles was performed using UV-Vis spectroscopy, FTIR, XRD, SEM, and EDX analysis.
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