Maximizing the potential applications of plasma electrolytic oxidation coatings produced on Mg-based alloys in anti-corrosion,antibacterial,and photocatalytic targeting through harnessing the LDH/PEO dual structure

There is an increasing interest in the development of Mg alloys,both for industrial and biomedical applications,due to their favorable characteristics such as being lightweight and robust.However,the inadequate corrosion resistance and lack of antibacterial properties pose significant challenges in the industrial and biomedical applications,necessitating the implementation of advanced coating engineering techniques.Plasma electrolytic oxidation(PEO)has emerged as a preferred coating technique because of its distinctive properties and successful surface modification results.However,there is a continuous need for further enhancements to optimize the performance and functionalities of protective surface treatments.The integration of layered double hydroxide(LDH)into PEO coatings on Mg alloys presents a promising approach to bolstering protective properties.This thorough review delves into the latest developments in integrating LDH into PEO coatings for corrosion-related purposes.It particularly emphasizes the significant improvements in corrosion resistance,antibacterial effectiveness,and photocatalytic performance resulting from the incorporation of LDH into PEO coatings.The two key mechanisms that enhance the corrosion resistance of PEO coatings containing LDH are the anion exchangeability of the LDH structure and the pore-sealing effect.Moreover,the antibacterial activity of PEO coatings with LDH stemmed from the release of antibacterial agents stored within the LDH structure,alterations in pH levels,and the photothermal conversion property.Furthermore,by incorporating LDH into PEO coatings,new opportunities emerge for tackling environmental issues through boosted photocatalytic properties,especially in the realm of pollutant degradation.

Photocatalytic degradation of methylene blue over MIL-100(Fe)/GO composites: a performance and kinetic study

Adsorption coupled with photocatalytic degradation is proposed to fulfill the removal and thorough elimination of organic dyes.Herein,we report a facile hydrothermal synthesis of MIL-100(Fe)/GO photocatalysts.The adsorption and photocatalytic degradation process of methylene blue(MB)on MIL‐100(Fe)/GO composites were systematically studied from performance and kinetic perspectives.A possible adsorption‐photocatalytic degradation mechanism is proposed.The optimized 1M8G composite achieves 95%MB removal(60.8 mg/g)in 210 min and displays well recyclability over ten cycles.The obtained MB adsorption and degradation results are well fitted onto Langmuir isotherm and pseudo‐second order kinetic model.This study shed light on the design of MOFs based composites for water treatment.

Photocatalytic application of magnesium spinel ferrite in wastewater remediation:A review

This review paper explores the efficacy of magnesium ferrite-based catalysts in photocatalytic degradation of organic contaminates(antibiotic and dyes).We report the influence of different doping strategies,synthesis methods,and composite materials on the degradation efficiency of these pollutants.Our analysis reveals the versatile and promising nature of magnesium ferrite-based catalysts,offering the valuable insights into their practical application for restoring the environment.Due to the smaller band gap and magnetic nature of magnesium ferrite,it holds the benefit of utilising the broader spectrum of light while also being recoverable.The in-depth analysis of magnesium ferrites'photocatalytic mechanism could lead to the development of cheap and reliable photocatalyst for the wastewater treatment.This concise review offers a thorough summary of the key advancements in this field,highlighting the pivotal role of the magnesium ferrite based photocatalysts in addressing the pressing global issue of organic pollutants in wastewater.

Preparation of Corncob-Like WO3 Nanomaterials and Their Photocatalytic Treatment of Toluene

Corn rod-like WO3 nanomaterials were successfully synthesized by a simple hydrothermal method. The morphology, structure and optical absorption properties of the prepared samples were characterized by SEM, XRD, FTIR and UV-Vis-DRS. The WO3 materials were corn rod-like morphology with about 800 nm for length and 150 nm for diameter, especially there were plenty of corn particles (about 20 nm) on the surface of corn rods. The X-ray diffraction peaks of the products corresponded with WO3 standard card, and the characteristic peak of W-O bond was found in the infrared spectrum. The absorption band edge of the products was about 480 nm, indicating their potential visible-light-induced photocatalytic activity. In situ FTIR technology research showed that the prepared WO3 nanomaterials had visible photocatalytic activity to gas-phase toluene. After a photocatalytic reaction for 8 hours toluene was effectively degraded, and carboxylic acid and aldehyde could be regarded as the intermediate products, and CO2 was produced as the final product during the reaction process.

Synthesis of CC/BiPO4/Bi2WO6 Composite Material and Its Photocatalytic Performance

Along with the popularity of environmental protection concepts, the environmental treatment of water pollution attracts widespread attention, among which, the research on Bi-based semiconductor photocatalytic degradation technology has made great progress. However, the development of such bismuth-based composites still remains a challenging task due to difficult recovery and low catalytic efficiency. Herein, a novel CC/BiPO4/Bi2WO6 composite was successfully synthesized through two-step hydrothermal method using activated flexible carbon cloth as a substrate. The results of the photocatalytic degradation experiments showed that the obtained CC/BiPO4/Bi2WO6 composites can degrade 92.1% RhB in 60 min under UV-visible light irradiation, which was much higher than that of unloaded BiPO4 (24.4%) and BiPO4/Bi2WO6 (52.9%), exhibiting a better adsorption-photocatalytic degradation performance than BiPO4 and BiPO4/Bi2WO6. Photoluminescence spectra indicated that the improved photocatalytic activity was due to the more effective inhibition of photogenerated carrier complexation. Furthermore, the radical capture experiments confirmed that h+, ·OH and O2- were the main active substances in the photocatalytic degradation process of RhB by the CC/BiPO4/Bi2WO6 composites. More importantly, the prepared CC/BiPO4/Bi2WO6 composite had a simple separation process and good recycling stability, and its photocatalytic degradation efficiency can still reach 53.3% after six cycles of RhB degradation. .

Recent developments in visible-light photocatalytic degradation of antibiotics

With the significant discharge of antibiotic wastewater into the aquatic and terrestrial ecosystems, antibiotic pollution has become a serious problem and presents a hazardous risk to the environment. To address such issues, various investigations on the removal of antibiotics have been undertaken. Photocatalysis has received tremendous attention owing to its great potential in removing antibiotics from aqueous solutions via a green, economic, and effective process. However, such a technology employing traditional photocatalysts suffers from major drawbacks such as light absorption being restricted to the UV spectrum only and fast charge recombination. To overcome these issues, considerable effort has been directed towards the development of advanced visible light-driven photocatalysts. This mini review summarises recent research progress in the state-of-the-art design and fabrication of photocatalysts with visible-light response for photocatalytic degradation of antibiotic wastewater. Such design strategies involve the doping of metal and non-metal into ultraviolet light-driven photocatalysts, development of new semiconductor photocatalysts, construction of heterojunction photocatalysts, and fabrication of surface plasmon resonance-enhanced photocatalytic systems. Additionally, some perspectives on the challenges and future developments in the area of photocatalytic degradation of antibiotics are provided.

Synthesis and highly efficient photocatalytic activity of mixed oxides derived from ZnNiAl layered double hydroxides

ZnO/NiO/ZnAl2O4 mixed-metal oxides were successfully synthesized through a hydrotalcite-like precursor route, in which appropriate amounts of metal salts solutions were mixed to obtain a new series of ZnNiAl layered double hydroxides（LDHs） as precursors, followed by calcination under different temperatures. The as-obtained samples were characterized by SEM, HRTEM, TEM, XRD, BET, TG-DTA, and UV-Vis spectra techniques. The photocatalytic activities of the samples were evaluated by degradation of methyl orange（MO） under the simulated sunlight irradiation. The effects of Zn/Ni/Al mole ratio and calcination temperature on the composition, morphology and photocatalytic activity of the samples were investigated in detail. The results indicated that compared with ZnNiAl-LDHs, the mixed-metal oxide showed superior photocatalytic performance for the degradation of MO. A maximum of 97.3% photocatalytic decoloration rate within 60 min was achieved from the LDH with the Zn/Ni/Al mole ratio of 2：1：1 and the calcination temperature of 500 ℃, which much exceeded that of Degussa P25 under the same conditions. The possible mechanism of photocatalytic degradation over ZnO/NiO/ZnAl2O4 was discussed.

Preparation of three-dimensional interconnected mesoporous anatase TiO_2-SiO_2 nanocomposites with high photocatalytic activities

In this article, we report the preparation of a three-dimensional（3D） interconnected mesoporous anatase TiO2-SiO2 nanocomposite. The nanocomposite was obtained by using an ordered two-dimensional（2D） hexagonal mesoporous anatase 70 TiO2-30 SiO2-950 nanocomposite（crystallized at 950 °C for 2 h） as a precursor, NaO H as an etchant of SiO2 via a ＂creating mesopores in the pore walls＂ approach. Our strategy adopts mild conditions of creating pores such as diluted NaO H solution, appropriate temperature and solid/liquid ratio, etc. aiming at ensuring the integrities of mesopores architecture and anatase nanocrystals. XRD, TEM and N2 sorption techniques have been used to systematically investigate the physico-chemical properties of the nanocomposites. The results show that the intrawall mesopores are highly dense and uniform（average pore size 3.6 nm）, and highly link the initial mesochannels in a 3D manner while retaining mesostructural integrity. There is no significant change to either crystallinity or size of the anatase nanocrystals before and after creating the intrawall mesopores. The photocatalytic degradation rates of rhodamine B（RhB, 0.303 min^–1） and methylene blue（MB, 0.757 min^–1） dyes on the resultant nanocomposite are very high, which are 5.1 and 5.3 times that of the precursor; even up to 16.5 and 24.1 times that of Degussa P25 photocatalyst, respectively. These results clearly demonstrate that the 3D interconnected mesopores structure plays an overwhelming role to the increments of activities. The 3D mesoporous anatase TiO2-SiO2 nanocomposite exhibits unexpected-high degradation activities to RhB and MB in the mesoporous metal oxide-based materials reported so far. Additionally, the nanocomposite is considerably stable and reusable. We believe that this method would pave the way for the preparation of other 3D highly interconnected mesoporous metal oxide-based materials with ultra-high performance.

Strong visible absorption and excellent photocatalytic performance of brown TiO_2 nanoparticles synthesized using one-step low-temperature process

particle size （5.0 nm）, large specific surface area （213.45 m1 2/g）, and efficient response to broadband light over the entire ultraviolet-visible spectrum with a narrow band gap of 1.84 eV. In addition, TiO2 -180℃ exhibited the optimal reaction rate constant for the degradation of methylene blue （0.08287 mg/（Lmin））, which is six times higher than that of the mixed rutile/anatase phase TiO2 photocatalytic standard P25 （0.01342 mg/（L min））. Furthermore, cycling photodegradation ex-periments confirmed the stability and reusability of this catalyst. The unique physicochemical properties resulting from the low-temperature preparation of TiO2 -180℃, including its broadband visible absorption associated with a high concentration of oxygen vacancies, large surface area, and enriched surface -OH/H2O may be responsible for this excellent photocatalytic performance. The use of as-prepared TiO2 -180℃ for practical applications is expected after further optimization.

Enhanced photocatalytic degradation of sulfadiazine by Fe^(3+) in aqueous TiO_2 suspension

In order to explore the reaction mechanism of Fe^3＋ and the mineralization effect of the micropollutant, Fe^3＋ assisted photocatalytic oxidation of sulfadiazine （SD） in the TiO2 suspended solution is investigated. The effect of Fe^3＋ participation, the degradation kinetics of SD, the effect of SD mineralization and the possible mechanism of Fe^3＋ participation in TiO2 suspension are analyzed by adding FeCl3, taking samples at a given time and determining the SD concentration. Results indicate that the degradation of SD catalyzed by TiO2/ Fe^3＋ is faster than that catalyzed by TiO2 or Fe^3＋ separately. The photocatalytic degradation of SD follows the pseudo-first- order kinetics model in a range of 20 to 80 mg/L of initial concentration. The mineralization rate of SD can be enhanced by the addition of Fe^3＋ in the TiO2 suspended solution. The mechanism of the rapid degradation of SD is proposed, which indicates that Fe^3＋ adsorbed on the surface of TiO2 particles acts as an electron acceptor. The amount of recombining electronhole pairs decreases, and the amount of hydroxyl radicals increases. The increased hydroxyl radical strengthens the degradation of SD in the TiO2/Fe^3＋ suspended solution.

Photocatalytic Degradation of Water-Soluble Dyes by LaCoO_3

Pervoskite type oxides LaCoO 3 was prepared by citrate method with the granula of 20 nm-30 nm. With a fluorescent Hg lamp or sunlight as irradiator, the degradation experiments of various water soluble dyes were carried out in the suspension system of LaCoO 3 . The results show that the pervoskite type oxide LaCoO 3 has good photocatalytic activity.Studied by X ray photoelectron spectroscopy and photoacoustic spectra, its photocatalytic activity is found to be related with factors such as the d electron structure of ion Co 3+ ,Co—O binding energy and adsorbed oxygen on the surface etc.

Effective multifunctional coatings with polyvinylpyrrolidone-enhanced ZIF-67 and zinc iron layered double hydroxide on microarc oxidation treated AZ31 magnesium alloy

Modulating metal-organic framework’s(MOF)crystallinity and size using a polymer,in conjunction with a high surface area of layered double hydroxide,yields an effective strategy for concurrently enhancing the electrochemical and photocatalytic performance.In this study,we present the development of an optimized nanocomposite,denoted as 0.5PVP/ZIF-67,developed on AZ31 magnesium alloy,serving as an efficient and durable multifunctional coating.This novel strategy aims to enhance the overall performance of the porous coating through the integration of microarc oxidation(MAO),ZnFe LDH backbone,and ZIF-67 formation facilitated by the addition of polyvinylpyrrolidone(PVP),resulting in a three-dimensional,highly efficient,and multifunctional material.The incorporation of 0.5 g of PVP proved to be effective in the size modulation of ZIF-67,which formed a corrosion-resistant top layer,improving the total polarization resistance(R_(p)=8.20×10^(8)).The dual functionality exhibited by this hybrid architecture positions it as a promising candidate for mitigating environmental pollution,degrading 97.93%of Rhodamine B dye in 45 min.Moreover,the sample displayed exceptional degradation efficiency(96.17%)after 5 cycles.This study illuminates the potential of nanocomposites as electrochemically stable and photocatalytically active materials,laying the foundation for the advancements of next-generation multifunctional frameworks.

Photocatalytic Degradation of Phenol over MWCNTs-TiO2 Composite Catalysts with Different Diameters

Titania-based composite catalysts were prepared through a sol-gel route employing multi-walled carbon nanotubes with different diameters. The materials were characterized using thermogravimetric analysis, nitrogen adsorption-desorption isotherm, powder X-ray diffraction, scanning electron microscopy, and diffuse reflectance UV-Vis absorption spectra. The application of the catalysts to photocatalytic degradation of phenol was tested under UV-Vis irradiation. A synergetic effect on phenol removal was observed in case of composite catalysts, which was evaluated in terms of apparent rate constant, total organic carbon removal and photonic efficiency.

Novel visible-light-responding InVO_4-Cu_2O-TiO_2 ternary nanoheterostructure: Preparation and photocatalytic characteristics

A novel visible-light-responding InVO4-Cu2O-TiO2 ternary nanoheterostructure was designed on the basis of the strategy of energy gap engineering and prepared through ordinary wet chemistry methods. The as-prepared nanoheterostructure was characterized by X-ray powder diffraction（XRD）, transmission electron microscopy（TEM）, high-resolution transmission electron microscopy（HRTEM） and diffuse reflectance ultraviolet-visible spectroscopy（UV-vis/DRS）. The TEM and HRTEM images of 10%InVO4-40%Cu2O-50%TiO2 confirm the formation of nanoheterostructures resulting from contact of the nanosized TiO2, Cu2O and InVO4 in the size of 5–20 nm in diameter. The InVO4-Cu2O-TiO2 nanoheterostructure, when compared with TiO2, Cu2O, InVO4, InVO4-TiO2 and Cu2O-TiO2, shows significant enhancement in the photocatalytic performance for the degradation of methyl orange（MO） under visible-light irradiation. With a 9 W energy-saving fluorescent lamp as the visible-light source, the MO degradation rate of 10%InVO4-40%Cu2O-50%TiO2 reaches close to 90% during 5 h, and the photocatalytic efficiency is maintained at over 90% after six cycles. This may be mainly ascribed to the matched bandgap configurations of TiO2, Cu2O and InVO4, and the formations of two p-n junctions by the p-type semiconductor Cu2O with the n-type semiconductors TiO2 and InVO4, all of which favor spatial photogenerated charge carrier separation. The X-ray photoelectron spectroscopy（XPS） characterization for the used 10%InVO4-40%Cu2O-50%TiO2 reveals that only a small shakeup satellite peak appears for Cu（II） species, implying bearable photocorrosion of Cu2O. This work could provide new insight into the design and preparation of novel visible-light-responding semiconductor composites.

Photocatalytic Degradation of Water-Soluble Dyes by LaCoO3

Pervoskite type oxides LaCoO 3 was prepared by citrate method with the granula of 20 nm-30 nm. With a fluorescent Hg lamp or sunlight as irradiator, the degradation experiments of various water soluble dyes were carried out in the suspension system of LaCoO 3 . The results show that the pervoskite type oxide LaCoO 3 has good photocatalytic activity.Studied by X ray photoelectron spectroscopy and photoacoustic spectra, its photocatalytic activity is found to be related with factors such as the d electron structure of ion Co 3+ ,Co—O binding energy and adsorbed oxygen on the surface etc.

Highly crystalline carbon nitride hollow spheres with enhanced photocatalytic performance

Graphitic carbon nitride(g-C_(3)N_(4))has emerged as a remarkably promising photocatalyst for addressing environmental and energy issues;however,it exhibits only moderate photocatalytic activity because of its low specific surface area and high recombination of carriers.Preparation of crystalline g-C_(3)N_(4) by the molten salt method has proven to be an effective method to improve the photocatalytic activity.However,crystalline g-C_(3)N_(4) prepared by the conventional molten salt method exhibits a less regular morphology.Herein,highly crystalline g-C_(3)N_(4) hollow spheres(CCNHS)were successfully prepared by the molten salt method using cyanuric acid-melamine as a precursor.The higher crystallization of the CCNHS samples not only repaired the structural defects at the surface of the CCNHS samples but also established a built-in electric field between heptazine-based g-C_(3)N_(4) and triazine-based g-C_(3)N_(4).The hollow structure improved the level of light energy utilization and increased the number of active sites for photocatalytic reactions.Because of the above characteristics,the as-prepared CCNHS samples simultaneously realized photocatalytic hydrogen evolution with the degradation of the plasticizer bisphenol A.This research offers a new perspective on the structural optimization of supramolecular self-assembly.

Photocatalytic degradation of the dye sulforhodamine-B: A comparative study of different light sources

The photocatalytic degradation of dye pollutant sulforhodamine-B （SRB） in aqueous titanium dioxide （TiO2） dispersions was examined under three lighting regimes： UV light （330 nm〈λ〈 380 nm）, sunlight, and visible light （λ〉450 nm）, all investigated at pH=2.5. Total organic carbon （TOC） and chemical oxygen demand （CODer） assays show that the degradation rate of SRB is much higher when irradiated with UV and sunlight compared with visible light. The temporal concentration changes of SRB illustrated a first-order reaction and the rate constant, k, is 0.197 min^-1, 0.152 min^-1, 0.027 min^-1, respectively, under the three lighting conditions. The final mineralized products were amine compounds identified by infrared spectrophotometry. When irradiated with visible light, the photocatalytic degradation rate could be improved by lowering the H2O2 concentration and inhibited by increasing the H2O2 concentration, but results contrary to the above were obtained when UV light was used for irradiation.

Photocatalytic Degradation of Water-Soluble Dyes by LaCoO_3

Perovskite type oxides LaCoO 3 was prepared by citrate method in granula of 20～30 nm. Using a fluorescent Hg lamp or sunlight as irradiator, the degradation experiments of various water soluble dyes were carried out in the suspension system of LaCoO 3. The results show that the perovskite type oxide LaCoO 3 has good photocatalytic activity. With the study of X ray photoelectron spectroscopy and photoacoustic spectra, its photocatalytic activity is mainly related with the factors such as the d electron structure of ion Co 3+ , Co O binding energy and adsorbed oxygen on the surface etc.

Photocatalytic degradation of dyes by AgBr/Ag_3PO_4 and the ecotoxicities of their degraded products

Ag3PO4 powders were prepared through a precipitation reaction between AgNO3 and precipitating agent solutions that were prepared by adjusting the amount of H3PO4 in the Na3PO4 solutions. The Ag3PO4 powders prepared from the precipitation solution with a pH of 6 showed the highest photocatalytic activity for decolorizing the methylene blue and rhodamine B dyes. These Ag3PO4 powders were further modified by the addition of KBr solutions to obtain AgBr/Ag3PO4 powders and these photocatalysts can decolorize the anionic dyes as reactive orange and methyl orange. The reactive species involved in the photocatalytic degradation process were evaluated for their inhibitory activity using the appropriate scavengers. After photocatalysis, mass spectrometry confirmed that the dyes were degraded to smaller molecules. The ecotoxicities of the dye solutions before and after treatment were evaluated by studying their ability to inhibit the growth of the bioindicator Chlorella vulgaris.

CdS-modified one-dimensional g-C_3N_4 porous nanotubes for efficient visible-light photocatalytic conversion

A heterojunction photocatalyst based on porous tubular g-C3N4 decorated with CdS nanoparticles was fabricated by a facile hydrothermal co-deposition method.The one-dimensional porous structure of g-C3N4 provides a higher specific surface area,enhanced light absorption,and better separation and transport performance of charge carriers along the longitudinal direction,all of which synergistically contribute to the superior photocatalytic activity observed.The significantly enhanced catalytic efficiency is also a benefit originating from the fast transfer of photogenerated electrons and holes between g-C3N4 and CdS through a built-in electric field,which was confirmed by investigating the morphology,structure,optical properties,electrochemical properties,and photocatalytic activities.Photocatalytic degradation of rhodamine B(RhB)and photocatalytic hydrogen evolution reaction were also carried out to investigate its photocatalytic performance.RhB can be degraded completely within 60 min,and the optimum H2 evolution rate of tubular g-C3N4/CdS composite is as high as 71.6μmol h^–1,which is about 16.3 times higher than that of pure bulk g-C3N4.The as-prepared nanostructure would be suitable for treating environmental pollutants as well as for water splitting.