To reduce the consumption of oxidant and catalyst in Fenton-like reaction and to realize the reuse of catalyst, yeast supported iron nanoparticles (nZVI@SC) was synthesized by tobacco leaf extract and applied in the heterogeneous Fenton-like degradation of aqueous methylene blue (MB) at ambient conditions. The performance of the composite was exploited in terms of catalytic activity and factors influencing MB degradation. The surface changes of nZVI@SC before and after reaction were characterized by XPS, SEM, FT-IR and XRD. Iron leaching, primary reactive oxidizing species, and the storage stability and reusability of catalyst were also investigated. Typically, 99.7% removal of 50 mg/L MB, with a TOC removal of 97.2%, could be achieved within 10 h by 0.1 g/L nZVI@SC coupled with 1.0 mM HO. The MB degradation is in good agreement with the pseudo-first-order model, and hydroxyl radicals in the bulk solution is the main reactive oxidizing species responsible for MB degradation. Based on the identified intermediates by liquid chromatography/mass spectrometry, the possible MB degradation mechanism in the nZVI@SC/HO system is discussed. The developed high-performance nZVI@SC catalyst strategy can provide a new route in enhancing the Fenton-like degradation of organic contaminants with less consumption of catalyst and oxidant.
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http://dx.doi.org/10.1016/j.ecoenv.2023.115240 | DOI Listing |
Carbohydr Polym
March 2025
Department of Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710061, China. Electronic address:
Cuproptosis shows great prospects in cancer treatments. However, insufficient intracellular copper amount, low-level redox homeostasis, and hypoxic tumor microenvironment severely restrict cuproptosis efficacy. Herein, hydrazided hyaluronan-templated decorated CuO-doxorubicin (CuDT) nanodot clusters (NCs) are developed for efficient doxorubicin (DOX)-sensitized cuproptosis therapy in breast cancer via a three-pronged strategy.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Institute of Translational Medicine, Medical College, Yangzhou University, Yangzhou 225001, China.
The intricacy, diversity, and heterogeneity of cancers make research focus on developing multimodal synergistic therapy strategies. Herein, an oxygen (O) self-feeding peroxisomal lactate oxidase (LOX)-based LOX-Ce6-Mn (LCM) was synthesized using a biomineralization approach, which was used for cascade chemodynamic therapy (CDT)/photodynamic therapy (PDT) combination therapies through dual depletion of lactate (Lac) and reactive oxygen species (ROS) generation. After endocytosis into tumor cells, the endogenous hydrogen peroxide (HO) can be converted to O by the catalase-like (CAT) activity of LCM, which can facilitate the catalytic reaction of LOX to consume more Lac and alleviate tumor hypoxia to enhance the generation of singlet oxygen (O) upon light irradiation.
View Article and Find Full Text PDFJ Hazard Mater
January 2025
College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing 210095, China. Electronic address:
Biochar (BC) possesses diverse active sites (e.g., oxygen-containing groups OCGs, defects, and electronegative heteroatom) responsible for the catalytic reactions.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
School of Chemistry & Materials Science, Jiangsu Normal University, 101 Shanghai Road, Xuzhou 221116, P. R. China.
Long-term inflammation and persistent bacterial infection are primary contributors to unhealed chronic wounds. The use of conventional antibiotics often leads to bacteria drug resistance, diminishing wound healing effectiveness. Nanozymes have become a promising alternative to antimicrobial materials due to their low cost, easy synthesis, and good stability.
View Article and Find Full Text PDFJ Pharm Sci
January 2025
Department of Pharmaceutical Chemistry, University of Kansas, 2093 Constant Avenue, Lawrence, KS 66047, USA. Electronic address:
Iron-catalyzed oxidation reactions are common degradation pathways in pharmaceutical formulations. Buffers can influence oxidation reactions promoted by iron (Fe) and hydrogen peroxide (H₂O₂). However, mechanistically, the specific role of buffers in such reactions is not well understood.
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