MgO Phase Research Articles

Spherical magnetic MgO-CeO2-Fe3O4@JB heterojunction for enhanced photodegradation of pesticide and complex anionic dyes: Understanding the degradation process and diverse water systems

Clothianidin (CLO) is a widely utilized pesticide recognized as an emerging pollutant capable of contaminating surface and subsurface water sources. Utilizing nanoparticles for photodegradation is a very ecological and cost-effective method for water treatment. This study involves the creation of a MgO-CeO2-Fe3O4@JB (Jute-Biochar) heterojunction with a mesoporous structure using hydrothermal process. The purpose of this design is to explore its potential for photocatalytic applications. PXRD (Powder X-ray Diffraction), FTIR (Fourier Transform Infrared), UV–DRS (Ultraviolet–Visible Diffuse Reflectance Spectroscopy), PL (Photoluminescence), TEM (Transmission Electron Microscopy), EDX (Energy Dispersive X-ray), XPS (X-ray Photoelectron Spectroscopy), VSM (Vibrating Sample Magnetometry), BET (Brunauer Emmett Teller), and SEM (Scanning Electron Microscopy) analysis confirmed the formation of a mesoporous MgO-CeO2-Fe3O4@JB heterojunction with preferred interface between MgO, CeO2, and Fe3O4 phases, extending the light-absorption insights to 700 nm. The photocatalytic performance of MgO-CeO2-Fe3O4@JB heterojunction was evaluated under visible-light using CLO as the target molecule. The degradation performances of CLO on MgO-CeO2-Fe3O4@JB were determined to be 95.24 ± 1.18 % after 35 min of exposure to light. The calculated rate constants for the degradation of CLO in presence of light using the MgO-CeO2-Fe3O4@JB composite were determined to be 0.0924 min−1. Furthermore, two complex dyes, Niagara Blue (NB) and Reactive Red (RR), photodegrade to 99.45 ± 1.24 % and 97.23 ± 1.41 % within 25 and 30 min, respectively. The excellent photocatalytic characteristics of the MgO-CeO2-Fe3O4@JB heterojunction were suggested to be primarily caused by the larger photo-response, aligned band-structure, and useful use of the photo-induced charge carriers of the photocatalyst. In addition, the recycling experiments have verified the exceptional photostability of the MgO-CeO2-Fe3O4@JB photocatalyst due to incorporation of nanoparticles into the biochar matrix. This leads to a synergistic mechanism for effectively eliminating these pollutants.

Characterization and 3D Reconstruction of the Crushing Behavior of SiO2–CaO–Al2O3–MgO Complex Inclusions in Spring Steel with High Basicity Slag Treatment

This article mainly studies the element content, phase composition, and fragmentation mechanism of SiO2–CaO–Al2O3–MgO composite inclusions that cause fatigue fracture of spring steel. The study found that the SiO2–CaO–Al2O3–MgO composite inclusions in the wire rod are not a homogeneous phase. According to the electron microscopy energy spectrum analysis results, although the SiO2–CaO–Al2O3–MgO composite inclusion is in the low‐melting‐point area of the phase diagram according to the component content ratio. However, field‐emission transmission electron microscopy analysis reveals that this type of composite inclusions includes MgAl2O4, CaAl2Si2O8, CaSiO3, MgSiO3, and a small amount of CaS. The Zeiss Crossbeam 550 electron microscope is used to conduct a three‐dimensional reconstruction analysis of this type of composite inclusions, which once again verified that the composition of this type of inclusions includes calcium silicate, MgAl2O4, MgO, and other phases. It is also found that there is a certain gap between the inclusions and the matrix, and the gap between the inclusions with high‐melting‐points such as MgAl2O4 and MgO and the matrix is more obvious. During the rolling process of SiO2–CaO–Al2O3–MgO composite inclusions, due to differences in hardness and deformation rate between different phases, the rolling process is deformed and fragmented for extended periods.

Synthesis of composite coatings based on Mg and Ti oxides by PEO for modulation of Mg corrosion resistance

In this study, the application of Plasma Electrolytic Oxidation (PEO) technique was investigated for fabricating composite coatings on magnesium (Mg) substrates aimed at modulating their corrosion resistance, an important characteristic for biodegradable orthopedic implants. The coatings were manufactured using an electrolytic solution containing MgO and TiO2 oxides, varying mass ratios, at currents of 30 mA and 200 mA. X-ray diffraction patterns confirmed the presence of TiO2 and MgO phases in the coatings, demonstrating the PEO capability to modulate the chemical composition by adjusting the mass ratio of oxides in the electrolytic solution. Microstructural analysis revealed decreased surface roughness with increasing TiO2 concentration. Corrosion tests indicated a significant improvement in corrosion resistance for all coatings compared to uncoated Mg substrate. In particularly, coatings with higher TiO2 concentrations, and those applied at a current density of 30 mA exhibited, enhanced corrosion resistance.

The Activation of Magnesium Sintering by Zinc Addition

Light alloys based on magnesium are widely used in most areas of science and technology. However, magnesium powder alloys are quite difficult to sinter due to the stable film of oxides that counteracts diffusion. Therefore, finding a method to activate magnesium sintering is urgent. This study examines the effect of adding 5 wt. % and 10 wt. % zinc to the sintering pattern of magnesium powders at 430 °C; a dwell of 30 min was used to homogenize at the densification’s temperature. Scanning electron microscopy (SEM) was used to characterize the alloy’s microstructure, while the phase composition was characterized using X-ray diffraction (XRD) and energy dispersion spectroscopy (EDS). The sintering densities of Mg–5Zn and Mg–10Zn were found to be 88% and 92%, respectively. The results show that after sintering, a heterophase structure of the alloy is formed based on a solid solution and phases MgZn and Mg50Zn21. To establish the sintering mechanism, the interaction at the MgO and Zn melt phase interface was analyzed using the sessile drop method. The minimum contact angle—65°—was discovered at 500 °C with a 20 min holding time. It was demonstrated that the sintering process in the Mg–Zn system proceeds through the following stages: (1) penetration of zinc into oxide-free surfaces; (2) crystallization of a solid solution, intermetallics; and (3) the removal of magnesium oxide from the particle surface, with oxide particles deposited on the surface of the sample.

Flame made low Pt loading catalysts supported on different metal oxides for catalytic combustion of CO and CH4

Catalytic combustion is an effective approach to remove air pollutants from various emission sources. For this purpose, supported noble metal catalysts are preferred in commercial applications due to their outstanding catalytic activity for eliminating CO, hydrocarbon compounds and NOx. In this paper, we employ the flame spray pyrolysis method to prepare a series of Pt-based catalysts with four different supports (TiO2, ZrO2, MgO and ZnO) and variable low Pt loadings for catalytic combustion of CO and CH4. The performance of 0.5 Pt/TiO2 is the best in all samples, in which the T90 temperatures are 107 and 500 °C for 90% conversion of CO and CH4, respectively. To examine its thermal stability, a time-on-stream test at 700 °C for 420 min is carried out, resulting in a decrease of about 5% in the final conversion of CH4. The X-ray diffraction results show that TiO2 support is a mixed phase with a major amount of anatase and a small amount of rutile other than a pure phase of ZrO2, MgO and ZnO. Furthermore, X-ray photoelectron spectroscopy analysis and high-angle annular dark-field scanning transmission electron microscopy observation show that when the Pt loading is low, the Pt species exist as highly dispersed single atoms on the surface of the TiO2 support. As the Pt loading gradually increases, the state of the Pt species transitions from single atoms to Pt clusters, resulting in a decrease in dispersion. Ultimately, the Pt can successfully accumulate on the surface of the TiO2 nanoparticles, providing abundant active sites for efficient catalytic combustion reactions.

Efficient Removal of Methylene Blue Dye from Aqueous Media Using Facilely Synthesized Magnesium Borate/Magnesium Oxide Nanostructures.

Methylene blue dye in water sources can pose health risks to humans, potentially causing methemoglobinemia, a condition that impairs the blood's ability to carry oxygen. Hence, the current study investigates the synthesis of novel magnesium borate/magnesium oxide (Mg3B2O6/MgO) nanostructures and their efficiency in removing methylene blue dye from aqueous media. The nanostructures were synthesized using the Pechini sol-gel method, which involves a reaction between magnesium nitrate hexahydrate and boric acid, with citric acid acting as a chelating agent and ethylene glycol as a crosslinker. This method helps in achieving a homogeneous mixture, which, upon calcination at 600 and 800 °C, yields Mg3B2O6/MgO novel nanostructures referred to as MB600 and MB800, respectively. The characterization of these nanostructures involved techniques like X-ray diffraction (XRD), Fourier-transform infrared (FTIR) spectroscopy, N2 gas analyzer, and field-emission scanning electron microscope (FE-SEM). These analyses confirmed the formation of orthorhombic Mg3B2O6 and cubic MgO phases with distinct features, influenced by the calcination temperature. The mean crystal size of the MB600 and MB800 samples was 64.57 and 79.20 nm, respectively. In addition, the BET surface area of the MB600 and MB800 samples was 74.63 and 64.82 m2/g, respectively. The results indicated that the MB600 sample, with its higher surface area, generally demonstrated better methylene blue dye removal performance (505.05 mg/g) than the MB800 sample (483.09 mg/g). The adsorption process followed the pseudo-second-order model, indicating dependency on available adsorption sites. Also, the adsorption process matched well with the Langmuir isotherm, confirming a homogeneous adsorbent surface. The thermodynamic parameters revealed that the adsorption process was physical, exothermic, and spontaneous. The MB600 and MB800 nanostructures could be effectively regenerated using 6 M HCl and reused across multiple cycles. These findings underscore the potential of these nanostructures as cost-effective and sustainable adsorbents for methylene blue dye removal.

Phosphorous recovery from sewage effluent by vanadium-substituted composite synthesized via reverse coprecipitation route

MgFe2O4/MgO (S-sample) and a novel V-modified MgFe2O4/MgO (V-sample) nanocomposites were successfully synthesized using the reverse coprecipitation method and were carefully characterized by X-ray diffractometry, Infrared and 57Fe Mössbauer spectroscopies, magnetization, electron microscopy (both transmission and scanning) and surface area analysis to comprehend their structural, morphological, hyperfine and magnetic properties before and after P adsorptions. MgFe2O4 and V-modified MgFe2O4 phases (with 30 nm average in “diameter”) govern the nanocomposite magnetic properties and these phases are chemically stable in phosphate-rich effluents. 50 nm in size MgO phase is responsible for P adsorption, but it showed chemical corrosion, as suggested by surface analysis. Adsorption kinetic revealed that there are two controlling steps: film and intraparticle diffusion. The nanocomposite materials fitted better to the Freundlich isotherm model, indicating that the adsorption site distribution for P is heterogeneous, and a multilayer adsorption mechanism is favored. Multicycle reuse experiments with secondary sewage effluent were performed, and the adsorption capability of the V-sample over 3 consecutive adsorption cycles was 11 mg g−1, a value 30 % higher than that found for the S-sample. The desorption efficiency of the V-sample was about 97 %, while the S-sample reached 76 %. The V-substituted composite is a promising nanoadsorbent for water remediation process in phosphate-rich effluents and should be also tested in remediation of other contaminants.

Effect of MgO content and CaO/Al2O3 ratio on melting temperature and viscosity of CaF2–CaO–Al2O3–MgO slag for electroslag remelting

During electroslag remelting (ESR), high MgO contents are typically added to CaF2–CaO–Al2O3 slag to control magnesium content in iron- and nickel-based alloys. The melting temperature and viscosity of ESR slag are pivotal for energy consumption, production efficiency, smooth operation, and ingot quality. However, there is currently a notable scarcity of research on the melting temperature and viscosity of CaF2–CaO–Al2O3–MgO slag with high MgO levels. Thus, the melting temperatures and viscosity of CaF2–CaO–Al2O3–MgO slags with varying MgO contents and CaO/Al2O3 (C/A) ratios were investigated. The results show that as the MgO content increases from 7.83 % to 13.18 %, the final precipitation content of the MgO phase significantly increases, resulting in an increase in the melting temperature from 1306 °C to 1319 °C. With the increase in the C/A ratio from 0.86 to 1.16, the precipitation completion temperatures of the Ca12Al14F2O32 and MgO phases significantly decrease and the MgAl2O4 phase transforms into the CaO phase. Hence, the melting temperature decreases from 1329 °C to 1314 °C. Further increasing the C/A ratio to 1.40, the final precipitation content of the CaO phase increases, resulting in a decrease in the melting temperature from 1314 °C to 1282 °C. Moreover, as the MgO content and C/A ratio increase, the slag viscosity exhibits different change trends within various temperature ranges. This depends on which of the depolymerization of the slag structure and the precipitation and clustering of the MgO phase has a greater effect on the slag viscosity.

PEMBUATAN PADUAN INTERMETALIK Mg2Si DENGAN DOPING BISMUTH SEBAGAI MATERIAL TERMOELEKTRIK

Increasing efficiency in gasoline fuel consumption in motorized vehicles is currently continuing. One way this is done is by making use of the energy that is lost during the combustion of a motorcycle engine. About half of the energy produced during burning will be lost due to heat energy and exhaust gases. This waste heat can be utilized by converting it into another form of energy. Thermoelectric materials are those that can convert heat energy into electricity directly. Thus, in this work, we synthesized the bismuth-doped Mg2Si thermoelectric material using a solid-state reaction method using a powder in a sealed tube technique. The initial step in the production process involves measuring the raw materials bismuth, silicon, and magnesium using the Mg2Si1-xBix formula (x = 0.00, 0.025, and 0.045). The raw material powder is grinded in a shaker mill before being sealed in a stainless steel tube. The powder is sealed in a tube and heated to 800 °C for 6 hours. According to XRD test results, the Mg2Si phase and Si and MgO phases have formed. The lattice constant of the cubic Mg2Si phase was found at ~0.636 nm. A SEM investigations of surface morphology suggest that bi-doping on Si sites influences grain size refinement. Therefore, it can be concluded that the Mg2Si intermetallic alloy production process was successfully completed.

Effect of Negative Pulse on the Stability of Black Electrolytes for Magnesium Alloy Microarc Oxidation.

The correlation between negative pulse and the black electrolyte properties of magnesium alloy micro-arc oxidation and the treated area was investigated by introducing a negative pulse electric field. The physical phase composition, microstructure, elemental distribution, and content of the coating were analyzed using X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS). The results showed that the introduction of negative pulses favored the generation of MgO and MgSiO3 contents in the coatings, and an increase in the MgO phase was found in the coatings formed in the failed electrolytes; the microporous size and microcracks of the coatings were gradually and significantly reduced; the average consumption of Cu ions was 0.0453 g/L·dm2, which is only 26% of that in the unipolar condition; the introduction of the negative pulses significantly improved the "anomalous consumption" of Cu ions. The introduction of negative pulse can significantly improve the "abnormal consumption" of copper ions, which is attributed to the change in the electric field by negative pulse, which makes the cathode-enriched Cu ions migrate to the anode and reduces the reduction and precipitation of Cu ions at the cathode.

Degradation of Methyl Red (MR) dye via fabricated Y2O3–MgO/g-C3N4 nanostructures: Modification of band gap and photocatalysis under visible light

In this study, graphitic carbon nitride (g-C3N4) composites with metal oxide nanoparticles (Y2O3, MgO) and their combination (CN, YCN, MCN and YMCN) were synthesized by an ultrasonic technique and were then characterized by different tools such as UV–Vis diffuse reflectance spectroscopy (DRS), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD) analysis and X-ray photoelectron spectroscopy (XPS). From the XRD diffractograms of the YMCN ternary composite, the g-C3N4, cubic MgO and Y2O3 structural phases were identified. The morphology of the as prepared nanostructure from the SEM analysis revealed the dispersion of the metal oxides nanoparticles with the graphitic sheets and the presence of the corresponding elements were confirmed by the EDX and XPS data. The FT–IR bands confirmed the bonding of the metal oxides to the nitride host as indicated by the characteristic modes. A reduction of the band gap energies was confirmed by the UV–Vis to indicate its visible light possible photoactivity. Accordingly, its visible light driven photocatalytic performance was assessed for methyl red degradation. The degradation competence was highest for the ternary composite YMCN due to the coupling of the semiconductors which increases the absorption and the charge carriers’ separation as well. The kinetics of degradation was best described by pseudo-first-order, and the most active species were the holes and the hydroxyl radicals. Thus, the YMCN nanocomposite is a visible light-active photocatalyst which can be engaged in the degradation of organic pollutants.

Improved bioactivity and corrosion resistance of NbO containing plasma electrolytic oxidation coating on ZM21 Mg alloy

ABSTRACT The present study reports the effect of niobium oxide (NbO) phase on the microstructure, corrosion, and bioactivity of coating on ZM21 Mg alloy by plasma electrolytic oxidation (PEO) process. NbO containing coatings are obtained by adding Potassium Niobate (KNbO3) along with the base electrolyte system, while the base electrolyte system consisted of sodium phosphate (Na3PO4⋅12 H2O) and potassium hydroxide (KOH). X-Ray Diffraction (XRD) was used for phase analysis, and Scanning Electron Microscopy (SEM) with Energy Dispersive X-ray Spectroscopy (EDS) was employed to extract the microstructural features. Tafel curves were generated to study the corrosion behaviour, and bioactivity test was conducted in the simulated body fluid (SBF) for 14 days to study the bioactivity. XRD results revealed that the PEO coatings consisted of MgO phase, whereas the sample coated in the electrolyte containing KNbO3 showed NbO phase in addition to MgO phase. NbO containing coating showed higher corrosion resistance and excellent bioactivity.

Efficient Rhodamine B dye uptake onto MgZrO3@g-C3N4 nanostructures: Fabrication and adsorption mechanism

Pristine graphitic carbon nitride (g-C3N4) was synthesized by calcination of urea under elevated temperature. A blend of g-C3N4 nanosheets and nanosized ZrO2 and MgO precursors were used to prepare MgZrO3@g-C3N4 hybrid nanocomposite (MZCN) then it was assessed for the adsorption of Rhodamine B (RhB) dye from aqueous solution. The X-ray diffraction analysis revealed the development of the monoclinic ZrO2, cubic MgO, and hexagonal graphitic carbon nitride phases. The energy diffraction X-rays (EDX), photoelectron electron, and Fourier transformed infrared (FT-IR) spectroscopy analyses collectively validated the formation of the presumed composite. An improved porosity with a surface area 35.86 m2.g−1 and pore volume 0.087 cm3.g−1 were determined by N2 adsorption setup. The adsorption kinetics fitted well with the pseudo-first-order model (R2 > 0.99), which designated an adsorption process influenced by physisorption. The kinetics models investigations revealed a film diffusion control of the adsorption process. The adsorption equilibrium matched perfectly with the Langmuir isotherm model (R2 > 0.99) marking a maximum adsorption capacity of 370.8 mg g−1, demonstrating outstanding monolayer adsorption process. In addition, the Freundlich constant (n = 1.76) value is falling in the range 1–10 suggested a favorable adsorption of RhB onto the composite surface. The mechanistic enquiry suggested van der Waal, hydrogen bonds and π–π electron–donor interactions between the electron-rich RhB and the functional groups in the adsorbent’s molecule. This work stipulates that MgZrO3@g-C3N4 holds promise as efficient adsorbent for organic dyes from contaminated wastewater.

Investigation on the interface bonding and reinforcement mechanism of nano Ti/AZ31 magnesium matrix composites

In this study, nano Ti/AZ31 composites were successfully prepared by powder metallurgy method, and the strength and plasticity of the composites were improved in both directions. The SEM shows that the Ti particles were evenly distributed at the grain boundary in the sintered composite, and the Ti particles pin the grain boundary to make the grain of the composite significantly refined. EBSD shows that the addition of nano Ti particles significantly reduces the texture strength of the composite and increases the starting probability of the slip system. TEM shows that nano Ti and AZ31 matrix formed stable Al3Ti and MgO phases at the interface, and shows a strong coherent relationship. The nanoindentation test shows that the Ti/AZ31 interface of the composite was stable, the interface bonding energy and interface fracture toughness were gradiently distributed, and the bonding energy and fracture toughness of the interface bonding area were better than those of the matrix. Tensile test shows that the 1.5 wt%Ti/AZ31 composite obtained the best comprehensive mechanical properties with yield strength, ultimate tensile strength and elongation of 143 MPa, 243 MPa and 11.5%, respectively, obviously higher than those of AZ31 alloys. The increased strength was mainly due to the grain refinement and strengthening at grain boundaries. The improved ductility was the result of weakened texture, increase of slip system start-up probability and strong interfacial bonding between Ti particles and AZ31 matrix.

Enhanced photocatalytic activity of α-Fe2O3/MgO nanocomposites for environmental sustainability

The goal of this study is to identify the optical, magnetic, and structural properties of α-Fe2O3/MgO & MgO/α-Fe2O3 nanocomposites and use them to purify water contaminated by harmful dyes. The economical hydrothermal approach was utilized to create nanocomposites, resulting in weight ratios of α-Fe2O3: MgO (1:1, 2:1 and 1:2). The synthesized materials containing α-Fe2O3 and MgO phases were identified by XRD pattern. XPS spectra were used to identify lattice defects and oxygen vacancies. The magnetic investigations show that pure α-Fe2O3 has a greater magnetic character than other synthesized materials, with a maximum magnetization of 0.14 × 10−2 emu/gm. In just 90 min, α-Fe2O3/MgO nanocomposites degrade Rose Bengal dye by 90.01 %, demonstrating their superior photocatalytic activity. The combined action of α-Fe2O3 and MgO, which prevents the formation of highly active radical species (OH• and O2• radicals) and photo-generated charge carrier recombination, is responsible for the increased photocatalytic activity. Furthermore, the magnetic nature of these nanocomposites enables them for the reusability process.

Understanding CO2 adsorption in layered double oxides synthesized by slag through kinetic and modelling techniques

As main by-product in iron and steel industry, high value-added utilization of blast furnace slag had received extensive attention. In this paper, a novelty technology was proposed for using blast furnace slag as raw material to obtain excellent CO2 adsorbent-layered double oxides. The characteristics of layered double hydroxides and layered double oxides were investigated in detailed. Most notably, the laminate structure of layered double hydroxides collapsed and the pore structure, particle size distribution and functional groups of the sample had been greatly changed. The layered double oxides were occupied by phases of CaO, Ca12Al14O32Cl2 and MgO. The transformation mechanism of the layered double oxides preparation was obtained. In addition, CO2 concentration and temperature influencing on CO2 adsorption of layered double oxides were studied and established a suitable kinetic model. The optimal kinetic mechanism model of CO2 adsorption by layered double oxides was PSO. The activation energy and pre-exponential factors were 56.88 kJ‧mol−1 and 12.26 min−1, respectively. Ultimately, CO2 adsorption capacity comparison and preliminary economic evaluation were conducted to assess the industrial feasibility of this technology. This work achieved the goals between CO2 reduction and high value-added utilization of solid waste in iron and steel industry.

Virtual substrate method: synthesis and growth kinetics of 2D metal oxide nanosheets

We present the experimental decomposition kinetics for the synthesis of metal oxide 2D nanosheets by the virtual substrate method. In this method, acetates of Mg and Cu were used as precursors for the growth of prototype MgO and CuO nanosheets, while the filter paper was utilized as a virtual substrate. The synthesized samples were characterized by X-ray diffraction for the phase analysis of the nanostructures, which confirms the cubic phase of MgO and monoclinic phase of CuO; with a minor Cu2O phase. Field emission scanning electron microscopy was used to determine the surface morphology of the nanosheets. Fourier transform infrared spectroscopy was utilized to identify the vibrational modes of the metal oxides and the functional groups present in the sample. Thermogravimetric analysis revealed the evolution of combustive oxidation of filter paper with the thermal decomposition of acetates situated on its surface.

The synthesis of MgO/Zein nanocomposites to improve anti-bacteria characteristics of mouthwash

Mouthwash is an alternative to address problems in the oral cavity, such as caries, periodontal inflammation, and microbial abscesses generally caused by pathogens. However, chlorhexidine contained in the mouthwash was limited concentration, i.e., 0.2 %, due to the side effects caused by these ingredients. Even though chlorhexidine has bactericidal and bacteriostatic properties against various bacteria found in plaque, for this reason, to increase the antibacterial activity of these mouthwashes, it is necessary to add other ingredients to the mouthwash formula, namely MgO/Zein nanocomposites with a composition of 1:4 and 1:5. The method used in this study was the preparation of MgO nanoparticles from dolomite using a solid acid solvent, the results of which were then composited with Zein using alcohol and NaOH. Synthesized samples were characterized using XRD, FTIR, SEM, and TEM. The antibacterial activity of S. aureus and mushrooms C. albicans in mouthwash with a concentration of 0.5 to 2.5 % can be determined by conducting a diffusion test. The results showed that the MgO/Zein nanocomposite fabrication had been successfully carried out and had the following characteristics: having a MgO phase with a polycrystalline cubic structure, having a zein phase with α-helix and β-sheet structures of proteins shows that Zein has an amorphous structure. The results of the antibacterial activity test showed that mouthwash with adding MgO/Zein nanocomposites more effectively inhibited bacterial growth of S. aureus and mushrooms C. albicans. It is known that the MgO/Zein nanocomposite composition 1:4 has the largest inhibition zone in S. aureus bacteria with a concentration of 1.5 % mouthwash and C. albicans fungi with a concentration of 0.5 %, namely 40.17 mm and 8.42 mm

MgAl Oxide Coatings Modified with CeO2 Particles Formed by Plasma Electrolytic Oxidation of AZ31 Magnesium Alloy: Photoluminescent and Photocatalytic Properties

MgAl oxide coatings composed of MgO and MgAl2O4 phases were doped with CeO2 particles via plasma electrolytic oxidation (PEO) of AZ31 magnesium alloy in a 5 g/L NaAlO2 water solution. Subsequently, particles of CeO2 up to 8 g/L were added. Extensive investigations were conducted to examine the morphology, the chemical and phase compositions, and, most importantly, the photoluminescent (PL) properties and photocatalytic activity (PA) during the photodegradation of methyl orange. The number of CeO2 particles incorporated into MgAl oxide coatings depends on the concentration of CeO2 particles in the aluminate electrolyte. However, the CeO2 particles do not significantly affect the thickness, phase structure, or surface morphology of the coatings. The PL emission spectrum of MgAl oxide coatings is divided into two bands: one in the 350–600 nm range related to structural defects in MgO, and another much more intense band in the 600–775 nm range attributed to the F+ centres in MgAl2O4. The incorporated CeO2 particles do not have a significant effect on the PL intensity of the band in the red spectral region, but the PL intensity of the first band increases with the concentration of CeO2 particles. The PA of MgAl/CeO2 oxide coatings is higher than that of pure MgAl oxide coatings. The MgAl/CeO2 oxide coating developed in aluminate electrolyte with a concentration of 2 g/L CeO2 particles exhibited the highest PA. The MgAl/CeO2 oxide coatings remained chemically and physically stable across multiple cycles, indicating their potential for applications.

Effect of ladle-lining materials on inclusion evolution in Al-killed steel during LF refining

Abstract The effect of lining materials (Al2O3 and Al2O3–MgO·Al2O3) of ladle on evolution of non-metallic inclusions in aluminum-killed (Al-killed) steel during ladle furnace refining without Ca treatment was investigated through industrial experiments. The results showed that non-metallic inclusions experienced the changes from Al2O3 → MgO–Al2O3 → CaO–Al2O3. During the refining process using either of the two ladle lining materials, for all non-metallic inclusions, the vast majority are distributed in the high Al2O3 area of the CaO–Al2O3–MgO phase diagram, with very little or none in the low melting point zone. Non-metallic inclusions are mainly smaller than 3 μm, while those larger than 3 μm consisted primarily of MgO·Al2O3 and CaO–Al2O3 inclusions. The use of an Al2O3–MgO·Al2O3-lining ladle is more effective in reducing the number density of inclusions in the steel. However, during the refining process, the Al2O3-lining ladle does not have a significant impact on the presence of MgO–Al2O3 and CaO–Al2O3 inclusions in the molten steel. The Al2O3–MgO·Al2O3-lining ladle does not have a significant effect on MgO–Al2O3 inclusions, but it does promote the formation of CaO–Al2O3 and CaS inclusions in the molten steel.