Iron sulfides have attracted growing concern in heterogeneous Fenton reaction. However, the structure of iron sulfides is different from that of iron oxides and how the structures affect the activation property of hydrogen peroxide (HO) remains unclear. This study investigated benzene removal through the activation of HO by the synthesized magnetite (FeO) and greigite (FeS). The structures of FeO and FeS were characterized by XRD and EPR, the electron transfer properties of FeO and FeS were analyzed by electrochemical workstation, XPS and DFT. It is revealed that the effective benzene removal rate of 88.86% in the FeS/HO was achieved, which compared to 15.58% obtainable from the FeO/HO, with the apparent rate constant in the FeS/HO being approximately 65 times over that in the FeO/HO. The better HO activation by FeS was attributed to the significant roles of S (-II) and S vacancies in regulating the dissolution of ferrous iron ions, thus generating abundant free •OH radical. In addition, surface bounded ferrous iron of FeS could transfer more electrons to HO and O to generate more surface bounded •OH and •O. This study revealed the combined action of dissolved and surface bounded ferrous iron of greigite on HO activation, and provides an efficient heterogeneous HO activator for the remediation of organic contaminants in groundwater.
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http://dx.doi.org/10.1016/j.chemosphere.2023.138111 | DOI Listing |
Phytopathology
January 2025
Guizhou University, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Huaxi District, Guiyang, Guizhou Province of China, Guiyang, China, 550025;
Gray mold is an important disease of crops and is widespread, harmful, difficult to control, and prone to developing fungicide resistance. Screening new fungicides is an important step in controlling this disease. Hydroxychloroquine is an anti-inflammatory and anti-malarial agent, which has shown marked inhibitory activity against many fungi in medicine.
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 PDFJ Phys Chem C Nanomater Interfaces
January 2025
Furman University, Greenville, South Carolina 29613, United States.
Surface-anchored metal-organic frameworks (surMOFs) are crystalline, nanoporous, supramolecular materials mounted to substrates that have the potential for integration within device architectures relevant for a variety of electronic, photonic, sensing, and gas storage applications. This research investigates the thin film formation of the Cu-BDC (copper benzene-1,4-dicarboxylate) MOF system on a carboxylic acid-terminated self-assembled monolayer by alternating deposition of solution-phase inorganic and organic precursors. X-ray diffraction (XRD) and atomic force microscopy (AFM) characterization demonstrate that crystalline Cu-BDC thin films are formed via Volmer-Weber growth.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
Department of Chemistry, Memorial University of Newfoundland, St. John's Newfoundland and Labrador, A1B 3X7, Canada.
The challenge with synthetically modified biochars is that they are notoriously difficult to characterize, and a new characterization approach that circumvents the challenges posed by overlapping bands in IR spectra is needed. We report multinuclear NMR approaches successful in the easy identification and quantification of covalently-bound functional groups on the biochar surface using P{H} CPMAS NMR spectroscopy.
View Article and Find Full Text PDFACS Nano
January 2025
IBM Almaden Research Center, 650 Harry Road, San Jose, California 95120, United States.
Lanthanide atoms show long magnetic lifetimes because of their strongly localized 4 electrons, but electrical control of their spins has been difficult because of their closed valence shell configurations. We achieved electron spin resonance of individual lanthanide atoms using a scanning tunneling microscope to probe the atoms bound to a protective insulating film. The atoms on this surface formed a singly charged cation state having an unpaired 6 electron, enabling tunnel current to access their 4 electrons.
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