Search Results (5)

Low-molecular-mass iron-reducing compounds (IRCs) were produced by entomopathogenic endophytic fungi Lecanicillium sp. ATA01 in liquid cultures. The extracellular hydrophilic extract contained three IRCs formed by peptides, iron and phenolate structures with molecular masses of 1207, 567 and 550 Da. These compounds were able to chelate and mediate the reduction of Fe⁺³ to Fe⁺² and oxidized recalcitrant lignin-model substrates such as veratryl alcohol (VA), 2,6-dimethoxyphenol (DMP), and 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulphonic acid (ABTS) with or without hydrogen peroxide. Besides, IRCs can promote the degradation of chlorophenols. The maximal degradation of p-chlorophenol, 2,4-dichlorophenol, 2,4,6-trichlorophenol, and pentachlorophenol was conducted at optimal degradation conditions for IRCs (pH 3.5, iron 100 mM, and H₂O₂ 10 mM). Furthermore, Fenton-like reactions using the synthetic iron chelates DTPA and EDTA and free Fe⁺² and Fe⁺³ were also carried out in order to compare with the reaction mediated by IRCs. The ferric IRCs displayed the ability to enhance the hydroxylation of chlorophenols as a part of a degradation mechanism of the IRC-assisted Fenton reaction. The complexed iron was more efficient than free iron in the Fenton-like reaction, and between them, the fungal chelates were more efficient than the synthetic mill chelates. Full article

A large amount of arsenic-containing solid waste is produced in the metallurgical process of heavy nonferrous metals (copper, lead, and zinc). The landfill disposal of these arsenic-containing solid waste will cause serious environmental problems and endanger people’s health. An electrochemical advanced oxidation experiment was carried out with the cathode modified by adding carbon black and polytetrafluoroethylene (PTFE) emulsion. The removal rate of arsenic using advanced electrochemical oxidation with the modified cathode in 75 g/L NaOH at 25 °C for 90 min reached 98.4%, which was significantly higher than 80.69% of the alkaline leaching arsenic removal process. The use of electrochemical advanced oxidation technology can efficiently deal with the problem of arsenic-containing toxic solid waste, considered as a cleaner and efficient method. Full article

Ferulic acid (FA) is used in skin formulations for protection against the damaging actions of the reactive oxygen species (ROS) produced by UVA radiation. Possible underlying protective mechanisms are not fully elucidated. By considering the kinetics of proton-coupled electron transfer (PCET) and radical-radical coupling (RRC) mechanisms, it appears that direct scavenging could be operative, providing that a high local concentration of FA is present at the place of ^•OH generation. The resulting FA phenoxyl radical, after the scavenging of a second ^•OH and keto-enol tautomerization of the intermediate, produces 5-hydroxyferulic acid (5OHFA). Inhibition of the lipoxygenase (LOX) enzyme, one of the enzymes that catalyse free radical production, by FA and 5OHFA were analysed. Results of molecular docking calculations indicate favourable binding interactions of FA and 5OHFA with the LOX active site. The exergonicity of chelation reactions of the catalytic Fe²⁺ ion with FA and 5OHFA indicate the potency of these chelators to prevent the formation of ^•OH radicals via Fenton-like reactions. The inhibition of the prooxidant LOX enzyme could be more relevant mechanism of skin protection against UVA induced oxidative stress than iron chelation and assumed direct scavenging of ROS. Full article

Advanced oxidation (e.g., fenton-like reagent oxidation and ozone oxidation) is a highly important technology that uses strong oxidizing free radicals to degrade organic pollutants and mineralize them. The fenton-like reactions have the characteristics of low cost, simple operation, thorough reaction and no secondary pollution. Fenton-like reagents refer to a strong oxidation system composed of transition metal ions (e.g., Fe³⁺, Mn²⁺ and Ag⁺) and oxidants (hydrogen peroxide, potassium persulfate, sodium persulfate, etc). Graphene and carbon nanotube possess a distinctive mechanical strength, flexibility, electrical and thermal conductivity and a very large specific surface area, which can work as an excellent carrier to disperse the catalyst and prevent its agglomeration. Fullerene can synergize with iron-based materials to promote the reaction of hydroxyl groups with organic pollutants and enhance the catalytic effect. Fenton-like catalysts influence the catalytic behavior by inducing electron transfer under strong interactions with the support. Due to the short lifespan of free radicals, the treatment effect is usually enhanced with the assistance of external conditions (ultraviolet and electric fields) to expand the application of fenton-like catalysts in water treatment. There are mainly light-fenton, electro-fenton and photoelectric-fenton methods. Fenton-like catalysts can be prepared by hydrothermal method, impregnation and coordination-precipitation approaches. The structures and properties of the catalysts are characterized by a variety of techniques, such as high-resolution transmission electron microscopy, high-angle annular dark-field scanning transmission electron microscopy and X-ray absorption near-edge structure spectroscopy. In this paper, we review the mechanisms, preparation methods, characterizations and applications status of fenton-like reagents in industrial wastewater treatment, and summarize the recycling of these catalysts and describe prospects for their future research directions. Full article

Fe⁰@Fe₃O₄ nanoparticles with dispersibility and stability better than single nano zero-valent iron (nZVI) were synthesized and combined with hydrogen peroxide to constitute a heterogeneous Fenton-like system, which was creatively applied in the degradation of 2,4-dichlorophenoxyacetic acid (2,4-D). The effects of different reaction conditions like pH, hydrogen peroxide concentration, temperature, and catalyst dosage on the removal of 2,4-D were evaluated. The target pollutant was completely removed in 90min; nearly 66% of them could be mineralized, and the main intermediate product was 2,4-dichlorophenol. Synergistic effects between nZVI and Fe₃O₄ made the 2,4-D degradation efficiency in the Fe⁰@Fe₃O₄/H₂O₂ system greater than in either of them alone. More than a supporter, Fe₃O₄ could facilitate the degradation process by releasing ferrous and ferric ions from the inner structure. The reduction of 2,4-D was mainly attributed to hydroxyl radicals including surface-bound ∙OH and free ∙OH in solution and was dominated by the former. The possible mechanism of this Fe⁰@Fe₃O₄ activated Fenton-like system was proposed. Full article