In the present work, palygorskite (PAL) supported Co-Fe oxides (CoFe@PAL) were prepared and used as a peroxymonosulfate (PMS) activator for removal of rhodamine B (RhB) in water. The results showed that CoFe@PAL prepared at impregnation solution of 50 g L and calcination temperature of 500 °C showed the best catalytic performance. The removal efficiency of RhB (10 mg L) by PMS (0.1 mmol L) activated with CoFe@PAL (1 g L) was above 98% within 60 min. The effects of various environmental factors including initial pH, humic acid (HA) and inorganic anions on the removal effect were simultaneously investigated. The radical quenching experiments and EPR characterization revealed that ˙OH, SO˙, O˙ and O radicals existed in the CoFe@PAL/PMS system simultaneously. The intermediates during RhB degradation were analyzed by LC-MS and possible degradation pathways of RhB were proposed. Moreover, CoFe@PAL exhibited superior stability and reusability.
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http://dx.doi.org/10.1039/d2ra07948h | DOI Listing |
Dalton Trans
January 2025
School of Chemical Engineering, Henan Center for Outstanding Overseas Scientists, Zhengzhou University, Zhengzhou 450001, China.
The efficient and environmentally friendly oxidation of biomass-based HMF to FDCA under mild conditions is highly desirable yet challenging. In this study, a series of CoFe alloy catalysts encapsulated in porous carbon (CoFe@NC) were synthesized using a solid-state synthesis method. By adjusting the Co/Fe ratio, an FDCA yield of 96.
View Article and Find Full Text PDFJ Colloid Interface Sci
March 2025
College of Resources and Environment, Key Laboratory of Agricultural Environment, National Engineering Research Center for Efficient Utilization of Soil and Fertilizer Resources, Shandong Agricultural University, Tai'an 271018, China. Electronic address:
Recently, antibiotic wastewater pollution has become increasingly serious. In this study, a novel hollow cubic framework self-supported nanoflower-like cathode catalyst (MoSe/CNC) based on Co Fe prussian blue analogues (CoFePBA)-derived cubic nanocage (CNC) loaded with MoSe was successfully prepared and utilized in an electro-activated peroxymonosulfate (PMS) system for norfloxacin (NOR) degradation. Benefit from the combined structures of MoSe, MoC, and Co/FeNC, the electrocatalytic activity and specific surface area were greatly improved.
View Article and Find Full Text PDFChemCatChem
June 2024
Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470, Mülheim an der Ruhr, Germany.
To test the ability of geochemical surfaces in serpentinizing hydrothermal systems to catalyze reactions from which metabolism arose, we investigated H-dependent CO reduction toward metabolic intermediates over silica-supported Co-Fe catalysts. Supported catalysts converted CO to various products at 180 °C and 2.0 MPa.
View Article and Find Full Text PDFChempluschem
January 2025
Institut de Ciència Molecular (ICMol), Universitat de València, Catedrático José Beltrán 2, 46980, Paterna, Spain.
The synthesis and characterization of a Co/Fe mixed-metal banana-shaped polyoxometalate with the formula [(CoFe(HO)PWO)(PWO)] (CoFe) is reported. This transition-metal-substituted polyoxometalate readily assembles from its components in a one-pot reaction and crystallizes in the monoclinic space group P2/c. The structure of CoFe can be considered a double sandwich composed by two B-α-{CoFePWO} Keggin units, in which one coordinatively saturated octahedral metal position is equally occupied by Co(II) and Fe(III) ions with a 50 % of site occupancy.
View Article and Find Full Text PDFACS Nano
October 2024
Materials Science and Engineering Program and Walker Department of Mechanical Engineering, The University of Texas at Austin, Austin, Texas 78712, United States.
Electrocatalytic CO reduction is garnering significant interest due to its potential applications in mitigating CO and producing fuel. However, the scaling up of related catalysis is still hindered by several challenges, including the cost of the catalytic materials, low selectivity, small current densities to maintain desirable selectivity. In this study, Fluorine (F) atoms were introduced into an N-doped carbon-supported single nickel (Ni) atom catalyst via facile polymer-assisted pyrolysis.
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