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Novel franklinite-like synthetic zinc-ferrite redox nanomaterial: synthesis, and evaluation for degradation of diclofenac in water.

ABSTRACT: The current study investigates a novel redox technology based on synthetic franklinite-like zinc-ferrite nanomaterial with magnetic properties and redox nature for potential use in water treatment. Physicochemical characterization revealed the nanoscale size and AB₂O₄ spinel configuration of the zinc-ferrite nanomaterial. The redox activity of nanoparticles was tested for degradation of diclofenac (DCF) pharmaceutical in water, without any added external oxidants and under dark experimental conditions. Results revealed ~90% degradation in DCF (10 μM) within 2 min of reaction using 0.17 g/L Zn_1.0Fe_2.0O₄. Degradation of DCF was due to chemical reduction by surface electrons on zinc-ferrite and oxidation by oxygen-based radicals. Three byproducts from reduction route and eight from oxidation pathways were identified in the reaction system. Reaction pathways were suggested based on the identified byproducts. Results demonstrated the magnetic zinc-ferrite is a standalone technology that has a great promise for rapid degradation of organic contaminants, such as DCF in water.

SUBMITTER: Al-Anazi A

PROVIDER: S-EPMC7787998 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Radiolytic redox interplay defines nanomaterial synthesis in liquids.

Project description:[Figure: see text].

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Microwave-Assisted Catalytic Degradation of Brilliant Green by Spinel Zinc Ferrite Sheets.

Project description:Microwave (MW)-assisted catalytic degradation, being an emerging technique, can potentially fill in the technological gap which promises on-demand, prompt, and efficient catalysis, and therefore, suitable MW catalysts are curiously being hunted. Candidature of spinel zinc ferrite (SZFO) atomic sheets as a MW catalyst has thoroughly been investigated in this article. Analytical techniques prove SZFO atomic sheets to be highly crystalline, thermally stable, good dielectric, and superparamagnetic, which render it a potentially strong MW catalyst. Brilliant green (BG) has been demonstrated to be chemisorbed on the SZFO atomic sheets, which upon MW irradiation gets mineralized within 5 min, and the overall efficiency has been observed to be >99%. Total organic carbon removal of ∼80% has been obtained. Ionic chromatography proves the formation of SO4 2- and NO3 - anions which increase with MW exposure time. Liquid chromatography mass spectroscopy studies have established intermediate formations during catalysis. SZFO, established as a uniquely suited and highly efficient MW catalyst for BG, is expected to broaden the horizons of MW-assisted catalytic degradation and lead it toward its broader applications.

| S-EPMC6648797 | biostudies-literature

Synthesis and Anticancer Properties of Water-Soluble Zinc Ionophores 2

Project description:We have demonstrated that water-soluble zinc ionophores can be administered to mice at relatively high doses and inhibit the growth of A549 lung cancer cells grown in xenograft models. Gene expression profiles of tumor specimens harvested from mice four hours after treatment confirmed that the activation of stress responsive genes occurs in vivo. These findings lead us to propose that the pharmacologic delivery of zinc to tumors using water solubilized ionophores is a potential approach to cancer therapy. Keywords: Dose response

2007-02-07 | GSE6962 | GEO

Synthesis and Anticancer Properties of Water-Soluble Zinc Ionophores 1

Project description:We have shown that water solubilized versions of a zinc ionophore increase intracellular concentrations of free zinc and have antiproliferative activity in exponential phase A549 lung cancer cultures. The gene expression profiles of A549 lung cancer cultures treated with the lead compound PCI-5002 reveal the activation of stress response pathways. Medium supplementation with zinc (25 μM) led to activation of additional oxidative stress response as well as apoptotic pathways. We propose that the pharmacologic delivery of zinc to tumors using water solubilized ionophores is a potential approach to cancer therapy. Keywords: Dose response

2007-02-07 | GSE6960 | GEO

Synthesis and Structural Studies of Manganese Ferrite and Zinc Ferrite Nanocomposites and Their Use as Photoadsorbents for Indigo Carmine and Methylene Blue Dyes.

Project description:Solar-moderated adsorptions of indigo carmine and methylene blue dyes were investigated using manganese and zinc ferrite capped with biochar prepared from the root of Chromolaena odorata. TEM micrograph of the as-prepared manganese ferrite nanocomposites (MnFe2O4@BC) revealed octagonally shaped particles with an average size of 42.64 nm while the zinc ferrite nanocomposite (ZnFe2O4@BC) micrograph revealed mixtures of rod- and cone-shaped particles with an average size of 43.82 nm. Biochar capping of MnFe2O4@BC reduced the band gap from 3.63 to 2.08 eV. The nanocomposite surface areas were 197.64 and 92.14 m2/g for MnFe2O4@BC and ZnFe2O4@BC, respectively. Photoadsorption of the as-prepared nanocomposites showed that 10 mg of ZnFe2O4@BC effectively removed 69.07 and 98.60% of 70 mg/L indigo carmine and methylene blue dyes while MnFe2O4@BC removed 77.65 and 94.83% of indigo carmine and methylene blue dyes after 2 h of equilibration under visible light irradiation, respectively. The nonlinear form of the Langmuir isotherm had a better approximation to the experimental solid-phase concentration (q e) for the adsorption of indigo carmine dye using both nanocomposites. In contrast, the linear form gave a better goodness-of-fit for the adsorptions of methylene blue dye. The manganese ferrite (MnFe2O4@BC) and zinc ferrite (ZnFe2O4@BC) nanocomposites showed no inhibition of Escherichia coli and Staphylococcus aureus, which indicates that they could be used for both biological and environmental applications.

| S-EPMC7758902 | biostudies-literature

Facile Synthesis of Porous Carbon for the Removal of Diclofenac Sodium from Water.

Project description:In this work, a series of porous carbon materials (PCs) were obtained at different carbonization temperatures (800, 900, 1000, and 1100 °C) by a simple and fast solvent-free method. Moreover, the feasibility of PCs as reliable and efficient adsorbents to capture diclofenac sodium (DCF) from the water was evaluated. Notably, porous carbon (PC) prepared at 1000 °C (PC-1000) was found to be the best candidate for the adsorption of DCF. Remarkably, adsorption equilibrium was achieved within 3 h, which followed a pseudo-second-order kinetic model with a high correlation coefficient (R 2 > 0.994). Furthermore, experimental data obtained from adsorption isotherm indicated that the capture of DCF onto PC-1000 followed the Langmuir adsorption model (R 2 > 0.997), wherein its maximum adsorption capacity was calculated to be 392 mg/g. In addition, based on the results obtained from the zeta potential of PC-1000 under different pH and the adsorbed quantity of DCF along with functional groups created on the surface of PC-1000, electrostatic and H-bonding interactions were proposed as the possible adsorption mechanisms. Due to its high stability and excellent reusability, PC-1000 has been testified as a promising candidate for removing DCF from contaminated water.

| S-EPMC6751710 | biostudies-literature

Nanomaterial Synthesis in Ionic Liquids and Their Use on the Photocatalytic Degradation of Emerging Pollutants.

Project description:The unique properties of ionic liquids make them suitable candidates to prepare nanoscale materials. A simple method that uses exclusively a corresponding bulk material and an ionic liquid-in this case, [P6,6,6,14]Cl-was used to prepare AgCl nanoparticles and AgCl@Fe3O4 or TiO2@Fe3O4 magnetic nanocomposites. The prepared nanomaterials were characterized by X-ray powder diffraction, scanning electron microscopy, transmission electron microscopy, ultraviolet-visible spectroscopy, and X-ray photoelectron spectroscopy. The photodegradation of atenolol as a model pharmaceutical pollutant in wastewater was investigated under ultraviolet-visible light irradiation using the different synthesized nanocatalysts. In the presence of 0.75 g·L-1 AgCl nanoparticles, a practically complete degradation of 10 ppm of atenolol was obtained after 30 min, following pseudo-first-order reaction kinetics. The effect of different variables (concentrations, pH, oxidant agents, etc.) was analyzed. The recyclability of the nanocatalyst was tested and found to be successful. A degradation mechanism was also proposed. In order to improve the recovery stage of the nanocatalyst, the use of magnetic nanocomposites is proposed. Under the same experimental conditions, a slightly lower and slower degradation was achieved with an easier separation. The main conclusions of the paper are the suitability of the use of ionic liquids to prepare different nanocatalysts and the effectiveness of these at degrading an emerging pollutant in wastewater treatment.

| S-EPMC7916080 | biostudies-literature

Synthesis and Anticancer Properties of Water-Soluble Zinc Ionophore: Cell Culture and Xenograft Model

Project description:This SuperSeries is composed of the SubSeries listed below.

2007-02-07 | GSE6972 | GEO

Synthesis and anticancer properties of water-soluble zinc ionophores.

Project description:Several water-solubilized versions of the zinc ionophore 1-hydroxypyridine-2-thione (ZnHPT), synthesized as part of the present study, have been found both to increase the intracellular concentrations of free zinc and to produce an antiproliferative activity in exponential phase A549 human lung cancer cultures. Gene expression profiles of A549 cultures treated with one of these water-soluble zinc ionophores, PCI-5002, reveal the activation of stress response pathways under the control of metal-responsive transcription factor 1 (MTF-1), hypoxia-inducible transcription factor 1 (HIF-1), and heat shock transcription factors. Additional oxidative stress response and apoptotic pathways were activated in cultures grown in zinc-supplemented media. We also show that these water-soluble zinc ionophores can be given to mice at 100 micromol/kg (300 micromol/m(2)) with no observable toxicity and inhibit the growth of A549 lung and PC3 prostate cancer cells grown in xenograft models. Gene expression profiles of tumor specimens harvested from mice 4 h after treatment confirmed the in vivo activation of MTF-1-responsive genes. Overall, we propose that water-solubilized zinc ionophores represent a potential new class of anticancer agents.

| S-EPMC3033660 | biostudies-literature

Tuning the Redox Properties of a Nonheme Iron(III)-Peroxo Complex Binding Redox-Inactive Zinc Ions by Water Molecules.

Project description:Redox-inactive metal ions play important roles in tuning chemical properties of metal-oxygen intermediates. Herein we report the effect of water molecules on the redox properties of a nonheme iron(III)-peroxo complex binding redox-inactive metal ions. The coordination of two water molecules to a Zn(2+) ion in (TMC)Fe(III) -(O2 )-Zn(CF3 SO3 )2 (1-Zn(2+) ) decreases the Lewis acidity of the Zn(2+) ion, resulting in the decrease of the one-electron oxidation and reduction potentials of 1-Zn(2+) . This further changes the reactivities of 1-Zn(2+) in oxidation and reduction reactions; no reaction occurred upon addition of an oxidant (e.g., cerium(IV) ammonium nitrate (CAN)) to 1-Zn(2+) , whereas 1-Zn(2+) coordinating two water molecules, (TMC)Fe(III) -(O2 )-Zn(CF3 SO3 )2 -(OH2 )2 [1-Zn(2+) -(OH2 )2 ], releases the O2 unit in the oxidation reaction. In the reduction reactions, 1-Zn(2+) was converted to its corresponding iron(IV)-oxo species upon addition of a reductant (e.g., a ferrocene derivative), whereas such a reaction occurred at a much slower rate in the case of 1-Zn(2+) -(OH2 )2 . The present results provide the first biomimetic example showing that water molecules at the active sites of metalloenzymes may participate in tuning the redox properties of metal-oxygen intermediates.

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