Magnetic recyclable visible light-driven Bi2WO6/Fe3O4/RGO for photocatalytic degradation of Microcystin-LR: Mechanism, pathway, and influencing factors.

Photocatalysis was an attractive strategy that had potential to tackle the Microcystin-LR (MC-LR) contamination of aquatic ecosystems. Herein, magnetic photocatalyst Fe3O4/Bi2WO6/Reduced graphene oxide composites (Bi2WO6/Fe3O4/RGO) were employed to degrade MC-LR. The removal efficiency and kinetic constant of the optimized Bi2WO6/Fe3O4/RGO (Bi2WO6/Fe3O4-40%/RGO) was 1.8 and 2.3 times stronger than the pure Bi2WO6. The improved activity of Bi2WO6/Fe3O4-40%/RGO was corresponded to the expanded visible light adsorption ability and reduction of photogenerated carrier recombination efficiency through the integration of Bi2WO6 and Fe3O4-40%/RGO. The MC-LR removal efficiency exhibited a positive tendency to the initial density of algae cells, fulvic acid, and the concentration of MC-LR decreased. The existed anions (Cl-, CO3-2, NO3-, H2PO4-) reduced MC-LR removal efficiency of Bi2WO6/Fe3O4-40%/RGO. The Bi2WO6/Fe3O4-40%/RGO could degrade 79.3% of MC-LR at pH = 7 after 180 min reaction process. The trapping experiments and ESR tests confirmed that the h+, ∙OH, and ∙O2- played a significant role in MC-LR degradation. The LC-MS/MS result revealed the intermediates and possible degradation pathways.

Directional Separation of Highly Reductive Electrons to the Reactive Center in a Magnetic S-Scheme ZnFe2O4/A-MoS2 Heterojunction for Enhanced Peroxymonosulfate Activation toward Pharmaceuticals and Personal Care Product Removal.

Pharmaceuticals and personal care products (PPCPs) are ubiquitous in sewage, adversely affecting ecosystems and human health. In this study, an S-scheme magnetic ZnFe2O4/ammoniated MoS2 (ZnFe2O4/A-MoS2) heterojunction as a visible-light-driven PMS activator for PPCP degradation was developed. ZnFe2O4/A-MoS2 achieves improved photocatalytic activity because the construction of S-scheme heterojunction promotes the separation of the highly reductive photogenerated electrons. The optimized photocatalyst (10%-ZnFe2O4/A-MoS2, 0.2 g/L) achieved 100% removal of 2 ppm carbamazepine (CBZ) within 2.5 min at a PMS dosage of 0.5 mM (initial pH 7.0). Mechanistic investigation revealed that the separated electrons to the ZnFe2O4 reactive center of the heterojunction facilitated PMS activation and generated SO4·- as the dominant reactive species for CBZ degradation. The system exhibited excellent practicability in various samples of actual sewage, where most sewage components negatively impacted CBZ degradation. Further, the chloride ions in high-salinity sewage could be activated to generate additional reactive chlorine species for PPCP degradation. The heterojunction possesses outstanding reusability and stability in treating various water conditions. This work provides mechanistic and practical perspectives in developing novel S-type heterojunctions for recalcitrant pollutant treatment.

Bifunctional quaternary magnetic composite as efficient heterojunctions photocatalyst for simultaneous photocatalytic visible light degradation of dye and herbicide pollutants from water and bacterial disinfection.

In the present study, the magnetic Fe3O4/Ag2C2O4/Ag3PO4/Ag nanocomposite were prepared through a simple co-precipitation method by using calendula officinalis seed extract as a stabilizer. The fabricated quaternary photocatalyst was applied for to degrade food dye Brilliant Blue FCF (BB) and herbicide Paraquat (PQ) as contaminants at binary mixture in a batch and continuous flow-loop photoreactor under visible light irradiation and also the antibacterial properties was investigated. The fabricated nanocomposite was determined by XRD, FESEM, EDX, BET&BJH, UV-DRS, FT-IR and VSM methods to gain insight about structure, morphology, purity, surface area, optical, functional group and magnetic properties. The photoelectrochemical experiments, PL and DRS indicate the successful coupling of the active semiconductors. The degradation efficiency of BB and PQ was announced to be 88.9% and 92.72% under optimal conditions with a high reaction rate constant value (0.03 and 0.0326 min-1), respectively. The quaternary photocatalyst exhibited superior photocatalytic performance compared with Ag3PO4/Ag2C2O4 and Ag2C2O4. Various scavengers were used to explore the mechanism of photocatalytic performance and supports that [Formula: see text] and OH. is main active species in the degradation process of BB and PQ, respectively. Furthermore, the Fe3O4/Ag2C2O4/Ag3PO4/Ag also demonstrated bactericidal activity against Staphylococcus aureus (S. aureus) as gram-positive bacteria and Escherichia coli (E. coli) as gram-negative bacteria.

Magnetic photocatalysts from δ-FeOOH and TiO2 and application in reactions for degradation of methylene blue and paracetamol with UV-C and sunlight.

Water contamination is a common problem, especially considering dyes and drugs disposal. A possible and effective treatment method to remove these organic pollutants from water is photocatalytic reaction. This study aimed to improve the photocatalytic properties of TiO2 using iron oxides (Ti/Fe composite). Different magnetic photocatalysts based on commercial TiO2 were obtained with 30, 50, and 80% (wt./wt.) of TiO2 supported on maghemite. X-ray diffraction with Rietveld refinement confirms the presence of γ-Fe2O3, α-Fe2O3, anatase, and rutile, as well as the relative percentages of the phases present in each photocatalyst. The magnetic properties were certified by VSM and sedimentation kinetics in the presence of a magnetic field. Besides their magnetic properties, UV-vis DRS shows that the obtained photocatalysts presented lower bandgap values when compared with TiO2. These factors allowed the materials to absorb radiation in the visible-light region and the separation from the reaction medium by the application of magnetic field. It was observed an enhancement of photodegradation reaction of methylene blue (MB) and paracetamol (PC). For example, when the content of TiO2 increased from 30 to 80% (wt./wt.), the efficiency increased from 58 to 99% (for MB) and 39 for 80% (for PC) under UV (λ = 254 nm). The reactions carried out with solar radiation showed 56 to 95% efficiency to discolor MB. In addition, the results of sedimentation kinetics and characterization confirmed the goals of the synthesis.

Self-assembly of TiO2/Fe3O4/SiO2 microbeads: A green approach to produce magnetic photocatalysts.

HYPOTHESIS: A green approach for producing magnetic photocatalysts via direct agglomeration of commercial nanoparticles in emulsion is shown. Aggregation is attributed to charge screening by salt addition which reduces stabilising repulsive forces between particles, and different nanoparticles (TiO2, Fe3O4 and SiO2) serve to imbue the final agglomerates with desired adsorption, photodegradation and magnetic properties. EXPERIMENT: Titania doped magnetic silica microbeads (TiO2/Fe3O4/SiO2) were produced at room temperature by CaCl2-induced aggregation of nanoparticles in a reverse emulsion template. The beads were characterized using optical microscopy, SEM, STEM, EDX and zeta potential measurements. The adsorption and photocatalytic properties of the system as well as its reusability were investigated using Rhodamine B and Methylene Blue as model pollutants. RESULTS: Magnetically responsive beads approximately 3-9 µm in diameter incorporating SiO2, TiO2 and Fe3O4 nanoparticles were produced. Adsorption and photodegradation properties of the beads were confirmed by bleaching solutions of Rhodamine B, Methylene Blue as well as mixtures of both dyes. Reusability of the beads after magnetic separation was demonstrated, exhibiting a dye removal efficiency greater than 93% per cycle for three consecutive cycles of UV-light irradiation. This method is simpler than conventional sol-gel methods and offers a green and easy to implement approach for producing structured functional materials.

Mono- and bimetallic (Pt/Cu) titanium(IV) oxide photocatalysts. Physicochemical and photocatalytic data of magnetic nanocomposites' shell.

Surface modification of titania with noble and semi-noble metals resulted in significant enhancement of photocatalytic activity. Presented data, showing the photocatalytic properties of TiO2-M (where M is Pt and/or Cu) photocatalysts were further used as Fe3O4@SiO2/TiO2-M magnetic nanocomposites shells in "Mono- and bimetallic (Pt/Cu) titanium(IV) oxide core-shell photocatalysts with Vis light activity and magnetic separability" [1]. Platinum and copper were photodeposited on four different titania matrices (commercial and self-obtained ones). The prepared photocatalysts were characterized by X-ray diffraction (XRD) analysis, specific surface area measurements using the Brunauer-Emmet-Teller (BET) isotherm, diffuse reflectance spectroscopy (DR-UV/Vis) analysis as well as scanning transmission electron microscopy (STEM) analysis. Photocatalytic properties were investigated in three different reactions: H2 generation, acetic acid oxidation to CO2, and phenol degradation.

Visible light-activated 1-D core-shell paramagnetic Fe-Ag@AgCl as an innovative method for photocatalytic inactivation of E. coli.

Innovative paramagnetic one-dimensional (1-D) core-shell Fe-Ag@AgCl visible light-driven photocatalysts are synthesized through a template-assisted electrodeposition method trailed by FeCl3 in-situ oxidation. The metallic nature of Fe-Ag@AgCl is confirmed through scanning electron microscopy (SEM) and crystal nature through X-ray diffraction (XRD). The controllable diameter of Fe-Ag is obtained through the selection of hollow size of the polycarbonate (PC) template. Electron impedance spectroscopy (EIS) confirms through the introduction of Fe to the Ag core that has prolonged the recombination of electron and hole. Escherichia coli (E. coli) are employed as the target bacteria to evaluate the photocatalytic disinfection performances. A total of 1.30 mg of Fe-Ag@AgCl is proved to be able to completely inactivate 107 CFU (colony forming units)/mL after 120 min of visible light irradiation. The transition electron microscopy (TEM) confirms the stability of the material after the photo reaction. As Fe-Ag@AgCl possesses magnetic properties, the material is recovered through the application of an external magnetic field. SEM images and results of 3D emission extraction matrix (EEM) depict that the bacteria cell death is caused by membrane permeability changes caused by the reduction of membrane associated proteins.

UV-Vis-Induced Degradation of Phenol over Magnetic Photocatalysts Modified with Pt, Pd, Cu and Au Nanoparticles.

The combination of TiO2 photocatalyst and magnetic oxide nanoparticles enhances the separation and recoverable properties of nanosized TiO2 photocatalyst. Metal-modified (Me = Pd, Au, Pt, Cu) TiO2/SiO2@Fe3O4 nanocomposites were prepared by an ultrasonic-assisted sol-gel method. All prepared samples were characterized by X-ray powder diffraction (XRD) analysis, Brunauer-Emmett-Teller (BET) method, X-ray photoelectron spectroscopy (XPS), scanning transmission electron microscopy (STEM), Mott-Schottky analysis and photoluminescence spectroscopy (PL). Phenol oxidation pathways of magnetic photocatalysts modified with Pt, Pd, Cu and Au nanoparticles proceeded by generation of reactive oxygen species, which oxidized phenol to benzoquinone, hydroquinone and catechol. Benzoquinone and maleic acid were products, which were determined in the hydroquinone oxidation pathway. The highest mineralization rate was observed for Pd-TiO2/SiO2@Fe3O4 and Cu-TiO2/SiO2@Fe3O4 photocatalysts, which produced the highest concentration of catechol during photocatalytic reaction. For Pt-TiO2/SiO2@Fe3O4 nanocomposite, a lack of catechol after 60 min of irradiation resulted in low mineralization rate (CO2 formation). It is proposed that the enhanced photocatalytic activity of palladium and copper-modified photocatalysts is related to an increase in the amount of adsorption sites and efficient charge carrier separation, whereas the keto-enol tautomeric equilibrium retards the rate of phenol photomineralization on Au-TiO2/SiO2@Fe3O4. The magnetization hysteresis loop indicated that the obtained hybrid photocatalyst showed magnetic properties and therefore could be easily separated after treatment process.

Visible-Light Active and Magnetically Recyclable Nanocomposites for the Degradation of Organic Dye.

Recyclable visible-light photocatalyst Fe3O4@TiO2 with core-shell structure was prepared by a simple synthetic strategy using solvothermal crystallization of titanium precursor on preformed Fe3O4 nanopartiles. The photo-degradation reaction of neutral red aqueous solution was tested to evaluate the visible-light photocatalytic activity of the as prepared Fe3O4@TiO2 nanoparticles, which show excellent photocatalytic activity compared with commercial P25 catalyst. Moreover, the Fe3O4@TiO2 nanocomposites can be easily separated from the reaction mixture, and maintain favorable photocatalytic activity after five cycles. The high visible light absorption of the Fe3O4@TiO2 nanocomposites may originate from the absence of electronic heterojunction, excellently dispersity and the high specific surface area of the as-synthesized Fe3O4@TiO2 samples.