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1.
Huan Jing Ke Xue ; 45(2): 898-908, 2024 Feb 08.
Article in Chinese | MEDLINE | ID: mdl-38471928

ABSTRACT

Magnetic phosphorous biochar (MPBC) was prepared from Camellia oleifera shells using phosphoric acid activation and iron co-deposition. The materials were characterized and analyzed through scanning electron microscopy (SEM), X-ray diffractometry (XRD), specific surface area and pore size analysis (BET), Fourier infrared spectroscopy (FT-IR), and X-ray photoelectron spectroscopy (XPS). MPBC had a high surface area (1 139.28 m2·g-1) and abundant surface functional groups, and it could achieve fast solid-liquid separation under the action of an external magnetic field. The adsorption behavior and influencing factors of sulfamethoxazole (SMX) in water were investigated. The adsorbent showed excellent adsorption properties for SMX under acidic and neutral conditions, and alkaline conditions and the presence of CO32- had obvious inhibition on adsorption. The adsorption process conformed to the quasi-second-order kinetics and Langmuir model. The adsorption rate was fast, and the maximum adsorption capacity reached 356.49 mg·g-1. The adsorption process was a spontaneous exothermic reaction, and low temperature was beneficial to the adsorption. The adsorption mechanism was mainly the chemisorption of pyrophosphate surface functional groups (C-O-P bond) between the SMX molecule and MPBC and also included hydrogen bonding, π-π electron donor-acceptor (π-πEDA) interaction, and a pore filling effect. The development of MPBC adsorbent provides an effective way for resource utilization of waste Camellia oleifera shells and treatment of sulfamethoxazole wastewater.


Subject(s)
Sulfamethoxazole , Water Pollutants, Chemical , Sulfamethoxazole/chemistry , Adsorption , Spectroscopy, Fourier Transform Infrared , Water , Water Pollutants, Chemical/analysis , Charcoal/chemistry , Phosphorus , Kinetics , Magnetic Phenomena
2.
Chemosphere ; 327: 138514, 2023 Jun.
Article in English | MEDLINE | ID: mdl-36972871

ABSTRACT

This study reported a novel application of Mn0.67Fe0.33-MOF-74 with two-dimensional (2D) morphology grown on carbon felt as a cathode for efficiently removing antibiotic sulfamethoxazole in the heterogeneous electro-Fenton system. Characterization demonstrated the successful synthesis of bimetallic MOF-74 by a simple one-step method. Electrochemical detection showed that the second metal addition and morphological change improved the electrochemical activity of the electrode and contributed to pollutant degradation. At pH 3 and 30 mA of current, the degradation efficiency of SMX reached 96% with 12.09 mg L-1 H2O2 and 0.21 mM ·OH detected in the system after 90 min. During the reaction, electron transfer between ≡FeII/III and ≡MnII/III promoted divalent metal ions regeneration, which ensured the continuation of the Fenton reaction. Two-dimensional structures exposed more active sites favoring ·OH production. The pathway of sulfamethoxazole degradation and the reaction mechanisms were proposed based on the intermediates identification by LC-MS and radical capture results. High degradation rates were still observed in tap and river water, revealing the potential of Mn0.67Fe0.33-MOF-74@CF for practical applications. This study provides a simple MOF-based cathode synthesis method, which enhances our understanding of constructing efficient electrocatalytic cathodes based on morphological design and multi-metal strategies.


Subject(s)
Sulfamethoxazole , Water Pollutants, Chemical , Manganese , Iron/chemistry , Hydrogen Peroxide/chemistry , Oxidation-Reduction , Electrodes , Water Pollutants, Chemical/analysis
3.
Sci Total Environ ; 804: 150096, 2022 Jan 15.
Article in English | MEDLINE | ID: mdl-34798724

ABSTRACT

Advanced oxidation processes (AOPs) have demonstrated an effective wastewater treatment method. But the application of AOPs using nanomaterials as catalysts is challenged with a series of problems, including limited mass transfer, surface fouling, poor stability, and difficult recycling. Recently, metal-organic frameworks (MOFs) with high tunability and ultrahigh porosity are emerging as excellent precursors for the delicate design of the structure/composition of catalysts and many MOF-derived catalysts with distinct physicochemical characteristics have shown optimized performance in various AOPs. Herein, to elucidate the structure-composition-performance relationship, a review on the performance optimization of MOF-derived catalysts to overcome the existing problems in AOPs by micro/macrostructure and multicomponent design is given. Impressively, MOF-derived strategy for the design of catalyst materials from the aspects of microstructure, macrostructure, and multicomponent (polymetallic, heteroatom doping, M/C hybrids, etc.) is firstly presented. Moreover, important advances of MOF-derived catalysts in the application of various AOPs (Fenton, persulfate-based AOPs, photocatalysis, electrochemical processes, hybrid AOPs) are summarized. The relationship between the unique micro/macrostructure and/or multicomponent features and performance optimization in mass transfer, catalytic efficiency, stability, and recyclability is clarified. Furthermore, the challenges and future work directions for the practical application of MOF-derived catalysts in AOPs for wastewater treatment are provided.


Subject(s)
Metal-Organic Frameworks , Nanostructures , Water Purification , Catalysis , Oxidation-Reduction
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