Magnesium Particles Research Articles

A New Wax Gourd (Benincasa hispida (Thunb.) Cogn.)‐Assisted Green Synthesis Method of Metal Oxides (TiO2, MgO)

AbstractIn the reaction environment of wax gourd extract, titanium dioxide (TiO2) and magnesium oxide (MgO) were synthesized by microemulsion method. Under atmospheric pressure, the optimum conditions for preparing TiO2 and MgO nanoparticles were investigated at different reaction temperatures and time. The obtained optimal reaction conditions are as follows: when the amount of TiCl3 solution was 70 µL, the mass ratio of wax gourd extract to water was 1:2, the reaction time was 60 min, and the reaction temperature was 35 °C, rod‐like TiO2 particles with the best dispersion and crystallinity were obtained. When the amount of MgCl2 solution was 10 mL, the amount of wax gourd extract was 40 mL, the reaction time was 120 min, and the reaction temperature was 70 °C, the prepared MgO particles exhibited a spindle shape with the best dispersion and crystallinity. Wax gourd‐assisted synthesis of TiO2 and MgO provides not only a new synthesis idea for the preparation of metal oxides, but also a green environmental protection system, which conforms to the concept of sustainable development.

Effects of Dolomitic Limestone on the Properties of Magnesium Oxysulfate Cement.

This study investigated the effects of substituting magnesium oxide (MgO) with dolomitic limestone (DL) on the mechanical and physical properties of magnesium oxysulfate (MOS) cement. Additionally, the hydration formation phases and the influence of the molar ratio on the MOS cement's performance were examined. The corresponding action mechanisms were identified and explored by compressive strength tests, scanning electron microscopy (SEM), X-ray diffraction (XRD), isothermal calorimetry, and a thermogravimetric analysis (TGA). The results showed that replacing MgO with DL decreased the reaction speed and heat release rate generated in the hydration process of the MOS cement. This substitution also reduced the quantity of non-hydrated MgO particles and delayed the formation of Mg(OH)2. The diminished formation of Mg(OH)2 contributed to an increase in the apparent porosity of pastes containing DL, thus alleviating internal stresses induced by Mg(OH)2 formation and enhancing their mechanical strength after 28 days of curing. Conversely, the increased porosity improved the CO2 diffusion within the structure, promoting the formation of magnesium carbonates (MgCO3). Through the characterization of the cement matrix (XRD and TGA), it was possible to identify phases, such as the brucite, periclase, and 318 phases. The obtained results revealed the potential of incorporating mineral fillers like limestone as a promising approach to producing MOS cement with a reduced environmental impact and better properties at higher curing ages.

Preparation of nano magnesium oxide by mechanochemical method using magnesium chloride

Magnesium chloride is a magnesium resource that is widely present in seawater and salt lakes. Therefore, the use of magnesium chloride is of great significance for the low-cost preparation of high-performance magnesium materials. In this work, mechanical ball milling was used for the preparation of magnesium oxide nanoparticles from magnesium chloride. Ball milling improves the unevenness of the reaction process and generates magnesium oxide with a more uniform particle size distribution. First, a magnesium chloride complex was obtained by heating and evaporating a mixture of magnesium chloride and ethanol with a mass ratio of 1:2 at 110 °C. Next, pure magnesium hydroxide with a smaller crystal size was obtained by ball milling the prepared magnesium chloride complex with calcium hydroxide at 600 rpm for 3 h. Finally, the magnesium hydroxide was calcined at 1000 °C for 60 min to obtain nano magnesium oxide particles with a particle size of 670 nm.

The role of calcium addition through powder sintering process in microstructure and mechanical behavior of a microalloyed magnesium

Calcium effectively strengthens magnesium through grain refinement when added in small quantities using the ingot metallurgy process. The extremely low solubility of calcium in magnesium restricts its addition using traditional powder metallurgy processes. However, the powder metallurgy process provides advantages like reduced material loss, properties control, and net-shape products. Hence, in this study, a diluted magnesium-calcium alloy was processed using the traditional blend-press-sinter (BPS) powder metallurgy process. Commercially pure magnesium was microalloyed with 0.4 wt% calcium. The sintered magnesium-calcium alloy was subjected to high-temperature extrusion. Microstructural characterization of the microalloyed Mg0.4Ca alloy revealed that the elemental calcium diffused into the magnesium particles during the sintering process and developed a gradient granular microstructure. The added initial calcium nanoparticles also acted as nucleation sites for magnesium during the sintering process. The gradient microstructure recrystallized and grew into equiaxed grains during the subsequent extrusion process. Mechanical properties characterization revealed that the addition of calcium as solute atoms increased the hardness, compressive strength, and ductility of magnesium, which was further enhanced by the extrusion process. The presence of calcium as solute atoms increased the tensile strength of extruded magnesium by a reasonable amount, while ductility remained almost unchanged.

Preservation of urine specimens for metabolic evaluation of recurrent urinary stone formers.

Stability of concentrations of urinary stone-related metabolites was analyzed from samples of recurrent urinary stone formers to assess necessity and effectiveness of urine acidification during collection and storage. First-morning urine was collected from 20 adult calcium-stone forming patients at Tomas Bata Hospital in the Czech Republic. Urine samples were analyzed for calcium, magnesium, inorganic phosphate, uric acid, sodium, potassium, chloride, citrate, oxalate, and urine particles. The single-voided specimens were collected without acidification, after which they were divided into three groups for storage: samples without acidification ("NON"), acidification before storage ("PRE"), or acidification after storage ("POST"). The analyses were conducted on the day of arrival (day 0, "baseline"), or after storage for 2 or 7days at room temperature. The maximum permissible difference (MPD) was defined as ±20 % from the baseline. The urine concentrations of all stone-related metabolites remained within the 20 % MPD limits in NON and POST samples after 2days, except for calcium in NON sample of one patient, and oxalate of three patients and citrate of one patient in POST samples. In PRE samples, stability failed in urine samples for oxalate of three patients, and for uric acid of four patients after 2days. Failures in stability often correlated with high baseline concentrations of those metabolites in urine. Detailed procedures are needed to collect urine specimens for analysis of urinary stone-related metabolites, considering both patient safety and stability of those metabolites. We recommend specific preservation steps.

One-step microwave-assisted synthesis of MgO-modified magnetic biochar for enhanced removal of lead and phosphate from wastewater: Performance and mechanisms

Herein, magnesium oxide (MgO) and ferroferric oxide (Fe3O4) functionalized biochar (MgO@MBC) was synthetized through one-step pyrolysis method, which was used to decontaminate lead (Pb) and phosphate in contaminated water. Characterization results exhibited that MgO and Fe3O4 particles were successfully loaded on MgO@MBC, and the magnetism of MgO@MBC was in favor of recycling materials. Experimental results showed that MgO@MBC possessed outstanding adsorption performance with 556.62/303.08 mg/g for Pb(II)/phosphate. Furthermore, MgO@MBC had excellent anti-interference performance under the coexistence of various ions, and superior reusability with over 82 % adsorption efficiency for Pb(II)/phosphate after four regeneration cycles. It demonstrated that the high-efficiency capacity of Pb(II) adsorbed on MgO@MBC was attributable to complexation, electrostatic attraction, precipitation, and pore-filling, while the efficient uptake of phosphate was due to precipitation, pore-filling, and ligand exchange. Based on the above analysis, MgO@MBC was believed to be an outstanding adsorbent for remediating Pb(II)/phosphate wastewater.

Green synthesis of Vitis vinifera extract-appended magnesium oxide NPs for biomedical applications

Abstract Biologically active magnesium oxide (MgO) nanoparticles were synthesised using green reduction with an extract derived from the Vitis vinifera plant. The investigation focused on examining the structure and carbon abundance resulting from the thermal degradation of adsorbed biomolecules. It was accomplished using powder X-ray diffraction, Raman spectroscopy, and FT-IR analysis techniques. X-ray photoelectron spectroscopy studies conducted on MgO nanoparticles indicate the absence of any supplementary peaks, thereby indicating the purity of the material. The morphological characteristics, which have been examined using field emission scanning electron microscopy and TEM methodologies, demonstrate the presence of particles with a spherical shape, exhibiting minimal agglomeration and a uniform distribution across the surfaces of MgO. The porous structure, porosity, and pore volume of the MgO particles were evaluated using Brunauer-Emmett-Teller surface analysis. The experimental findings reveal that the surface area of the MgO nanoparticles is 23.8742 m2/g, while the total pore volume is 0.12528 cm3/g. Additionally, the average pore diameter is determined to be 1.7 nm. These observations collectively suggest the presence of microporous structures within the MgO nanoparticles. This article discusses the biological studies to assess the antibacterial, antifungal, anti-inflammatory, and anti-diabetic activities of the synthesised MgO nanoparticles.

Promotional effect of NaNO3/NaNO2 on CO2 adsorption performance of MgO sorbents

The magnesium oxide (MgO) sorbents doped with different NaNO3/NaNO2 molar ratios were prepared to improve their stability over multiple cycles. Regulating the NaNO3/NaNO2 molar ratio effectively improved the CO2 adsorption performance of the sorbent. The MgO sorbent with the NaNO3/NaNO2 molar ratio of 0.8 exhibited outstanding performance and stability. Characterization and density functional theory calculations confirmed the positive effects of the appropriate NaNO3 amount in improving the adsorption activity, whereas the suitable NaNO2 amount slowed the sintering step and improved stability. Notably, the molten salt remained stable during cycling and did not decompose even at high regeneration temperatures, guaranteeing the cyclic stability of the sorbent. Further characterization showed that the CO2 sorption drop in the first few cycles was ascribed to the decline in the active surface owing to the aggregation of MgO particles, incomplete regeneration of sorbents, and segregation of molten salt on the sorbent surface.

Combustion of single micron-sized magnesium particles in carbon dioxide

An experimental system integrating micro-sized single particle generation, ignition, and observation was proposed and constructed for investigating the combustion characteristics of magnesium single particles in carbon dioxide. Defining the onset of combustion using the boiling point temperature allows for precise measurement of combustion time without artificial interference. Results revealed four modes of combustion for magnesium particles (Vapor-phase combustion, surface reaction, Micro explosion and flash-out mode) in carbon dioxide. Vapor-phase combustion is diffusion-controlled (with a D01.76 scaling, where D0 is the initial particle diameter). Additionally, the micro-explosion mode primarily occurs in particles with diameters exceeding 70 μm, and the combustion time is rather insensitive to the particle size (Typically 0.5 ∼ 2.2 ms in this study). The characteristic temperatures of the particles were determined using two-color pyrometry, indicating that the particle combustion temperature decreases with increasing particle size. Magnesium particles typically reach temperatures approximately 800 K higher than normal vapor-phase combustion temperatures before experiencing micro-explosions. Analysis of combustion products shows that the oxide shell formed by the combustion of magnesium particles has a three-layer structure. Both the outer and inner layers are mixed layers of magnesium oxide and solid carbon produced during combustion reactions, and the middle layer is the initial oxidation layer of the particles.

An experimental investigation of the convective heat transfer augmentation in U-bend double pipe heat exchanger using water-MgO-Cmc fluid

One of the major problems of using nanofluids in heat exchange applications is the forming and deposition of nanoparticles on the inner surface of the heat exchanger. In this paper, Water-Cmc fluid is used as a surfactant for nanoparticles to prevent deposition and congregation. The pressure drops and heat transfer in U-bend double pipe heat exchanger based on water-MgO-Cmc fluid, are examined. Nanoparticles of Magnesium Oxide (MgO) and Carboxymethyl Cellulose (Cmc) are used with pure water as a base fluid. The experimental rig and procedures are designed to facilitate various operational conditions such as flow rate, volume concentration of MgO particles and weight concentration of Cmc particles. Furthermore, convective heat transfer coefficient, heat exchanger effectiveness, pressure drop, friction factor, under different conditions, are measured. The results demonstrate convective heat transfer coefficient of U-bend double pipe heat exchangers is enhanced by 35% for 1 MgO vol.% and 0.2 Cmc wt.% compared to base fluid (Water-Cmc). It is concluded that pressure drops are directly proportion to the increase of MgO nanoparticles at same Cmc concentration by 23% at 0.2 wt.%. Whilst, friction factor of the system is inversely proportion to the increase of volumetric flow rate of water-MgO-Cmc fluid. An increase in MgO nanoparticle concentration increases the friction factor, hence maximum friction factor enhancement by 38% for MgO concentration of 1 vol.%. The effectiveness of heat exchanger is slightly increased by 8% with increase of MgO concentration and flow rate. Finally, thermo-physical characteristics of water-MgO-Cmc fluid at various temperatures, are measured

Analytical assessment of hetero-/homogeneous combustion of magnesium particle: Fully explicit formulas for flame characteristics

In this study, by proposing a comprehensive multi-step model, the combustion of magnesium particles in O2-He, O2-Ar, and O2-N2 is scrutinized. In the current model, both the heterogeneous and homogeneous combustions are considered and the process is divided into four stages solid, liquid, and gas combustion and melting. Moreover, the diffusions of oxygen and unreacted magnesium to droplet and infinity together with surface exothermic reaction are considered. The governing equations are analytically solved and then, the formulas are extracted for combustion time and temperature, flame standoff distance, and evaporation rate as the functions of particle diameter, ambient temperature and pressure, oxygen mass fraction, type of inert gas, and Lewis numbers. For 120 µm particle and oxygen content of 0.05, time contributions of homogeneous and heterogeneous combustions are 85.8% and 14.2%, respectively. The burning time has drastic changes at ambient pressures below l atm, so that the burning time variations relative to the pressure in the environments less than 1 atm and greater than it are equal to 1200–1550 and 70–90 ms/atm, respectively. When the oxygen mass fraction is less than 0.29, combustion in helium-oxygen ends earlier than that in O2-Ar and O2-N2, but for the mass fraction greater than 0.35, it has the longest burning time.

Synthesis of Mg2FeH6 by High‐Temperature High‐Pressure Reactive Planetary Ball Milling

Herein, a new approach for the synthesis of metal hydrides using simultaneous high‐temperature and high‐pressure reactive ball milling is demonstrated by preparing ternary magnesium iron hydride. The novelty and uniqueness of this technique are based on its integration of a specially designed and manufactured milling vial, allowing synthesis at controlled elevated temperatures (room temperature [RT]–400 °C) and pressures up to 100 bar. A Mg and Fe (2:1) mixture is used as a substrate for Mg2FeH6 synthesis. The effects of temperature on the synthesis kinetics and their outcomes are examined. An increase in the temperature accelerates the kinetics of hydrogen absorption for MgH2, while Mg2FeH6 formation is observed only above 250 °C. Increasing the reaction temperature not only causes magnesium particle refinement due to the hydrogenation and formation of magnesium hydrides but also leads to the agglomeration of iron caused by plastification due to a lack of strain hardening. The maximum conversion to Mg2FeH6 is observed for the sample premilled at RT. In this work, it is revealed that additional physical variables, e.g., pressure, temperature, time, and milling speed, during mechanochemical synthesis and material properties, need to be evaluated and considered to improve the reaction kinetics and yield of the synthesis.

Effect of process parameters on microstructure and Raman characteristics of magnesium doped ZnO thin films

MgxZn1-xO thin films were prepared on glass substrates by radio frequency magnetron sputtering under different sputtering processes. The surface morphology, microstructure, and Raman characteristics of the films were studied using scanning electron microscopy (SEM), X-ray diffraction (XRD), and Raman Spectrometer. The results show that an increase in the O/Ar ratio decreases the surface smoothness of the thin film and worsens the particle uniformity. The particles of undoped Magnesium doped Zinc Oxide (ZnO) films are small and uniform, and the uniformity of the particles in the films becomes worse after doping. Moreover, there are multiple diffraction peaks in the magnesium doped Zinc Oxide films, presenting a polycrystalline state, but the diffraction peak positions do not significantly change with the concentration and intensity of magnesium doped. The Raman characteristic peak undergoes a blue shift with the increase of magnesium doping concentration, and the peak position shifts from 573 cm−1 to 607 cm−1.

Basic magnesium sulfate@TiO2 composite for efficient adsorption and photocatalytic degradation of 4-dodecylmorpholine in brine

More than 70% of the potash fertilizer globally is produced by the froth flotation process, in which 4-dodecylmorpholine (DMP) serves as a reverse flotation agent. As the potash fertilizer production rapidly rises, the increased DMP levels in discharged brine pose a threat to the production of high-value chemicals. In this paper, composite particles of basic magnesium sulfate@TiO2 (BMS@TiO2) were prepared using a simple and mild loading method. These particles were utilized for the adsorption and photocatalytic degradation of DMP in brine. Compared with normal powdered materials, the granular BMS@TiO2 in this study can be easily separated from liquid, and the degradation intermediates will not enter the brine without causing secondary pollution. BMS@TiO2 consists of 5·1·7 phase (5Mg(OH)2·MgSO4·7H2O) whisker clusters embedding 2.3% TiO2. The adsorption equilibrium of DMP on BMS@TiO2 particles was achieved through hydrogen bonding and pore interception with the adsorption capacity of approximately 5 mg g−1 after 6 h. The photodegradation efficiency of DMP adsorbed on BMS@TiO2 reached about 92% within 16 h, which is compared with that of pure TiO2 nanoparticles. Additionally, excellent stability and recyclability of BMS@TiO2 were also observed in five cycle tests of adsorption and photocatalytic degradation of DMP, and the possible photocatalytic degradation pathways and mechanism of DMP are proposed following molecular electrostatic potential analysis. This work provides a sustainable and environmentally friendly approach for eliminating organic micropollutants from water environments.

Direct observation and elemental analysis of material nanoparticles in solution using scanning electron-assisted dielectric microscopy and EDS

High-resolution observation and elemental analysis of various particles in solution are important in the fields of materials, analytical chemistry, and industrial applications. Analysis of slurries of raw materials is essential for the development of highly functional materials. Recently, we have developed an SEM-based scanning electron assisted dielectric microscope (SE-ADM), which can directly observe biological samples and organic materials in aqueous solutions. Here, we have developed an SE-ADM system with the addition of energy-dispersive x-ray spectrometry that enables direct observation and elemental analysis of nanoparticles in solution. Using this system, we were able to directly observe and conduct elemental analysis of ceramic slurries and to clarify the dispersion state of alumina particles in solution, the distribution of binder, and the bonding state of silica and magnesium particles. Furthermore, our system can be applied to diverse liquid samples across a broad range of scientific and industrial fields, for example, nanotubes, organic specimens, batteries, and catalytic materials.

Behaviors and Reaction Mechanism of MgO Particles in Lithium Niobate Matrix

A congruent lithium niobate crystal doped with MgO particles was grown and processed. By scanning electron microscope (SEM), it can be seen that magnesium oxide exists in the form of inclusion in the crystal matrix. The mapping function of the electron probe can detect the element composition of the inclusions. The samples required for transmission electron microscope(TEM) were prepared by ion thinning method. The magnesium oxide particles were found by TEM, and the lattice phase at the interface between magnesium oxide and lithium niobate was obtained. The lattice phase analysis confirms that magnesium oxide can enter the lattice of lithium niobate in the form of ions. Finally, the sample was observed by piezoresponse force microscopy.

Investigating the anti-inflammatory and bone repair-promoting effects of an injectable porous hydrogel containing magnesium ions in a rat periodontitis mode

Periodontitis is associated with several systemic diseases, and advanced periodontitis is often linked to an extensive inflammatory microenvironment and irregularly shaped alveolar bone defects. However, eliminating periodontal inflammation in a minimally invasive manner while repairing irregularly shaped bone defects is clinically challenging. In comparison to traditional bone grafts, a thermo-sensitive hydrogel can be injected into deep periodontal pockets, forming and filling the alveolar bone defects in situ. In this study, porous injectable thermo-sensitive hydrogels containing magnesium ions were prepared by adding magnesium particles (MPs) to a glycerophosphate solution and combining this mixture with a chitosan solution. The incorporation of MPs created interconnected pores in the hydrogel, exhibiting high cytocompatibility and maintaining cell viability, proliferation, spreading, and osteogenesis in vitro. Evaluation on an experimental periodontitis rat model, using micro-computed tomography and histological analyses, demonstrated that this Mg2+-containing hydrogel effectively reduced periodontal inflammation, inhibited osteoclast activity, and partially repaired inflammation-induced alveolar bone loss. These results suggest that Mg2+-containing thermo-sensitive porous hydrogels might be promising candidates for treating periodontitis.

Mechanical properties and wear characterization of Al-Mg composites synthesized at different temperatures

<abstract> <p>Reactive sintering of Al-Mg powder mixtures containing 5, 10, 15, and 20 wt.% Mg was used to synthesize lightweight composites reinforced with in-situ formed Al<sub>3</sub>Mg<sub>2</sub> and Al<sub>12</sub>Mg<sub>17</sub> intermetallics. Detailed microstructural investigation and phase analysis were employed to examine the phases in the composites formed at 400 and 450 ℃. The creation of particles with the Al<sub>12</sub>Mg<sub>17</sub> cores encapsulated by the Al<sub>3</sub>Mg<sub>2</sub> phase, which was further covered by a continuous aluminum matrix, was observed in the composites synthesized at 400 ℃. If the composites were held at 450 ℃, the liquid phase appeared at the Al-Mg interface, and as a result, a two-phase mixture was formed. It was the eutectic composed of the Al<sub>3</sub>Mg<sub>2</sub> intermetallic compound and a solid solution of magnesium in aluminum (Al). The introduction of magnesium particles into the aluminum matrix resulted in a decrease in the density of composites, but there was no significant difference in the density of composites sintered at different temperatures. The mechanical behavior of the composites was examined using microhardness and hardness measurements and a room-temperature compression test. The result of using different cooling speeds, with the furnace and quenching in water, was the refining of the grains in the Al<sub>3</sub>Mg<sub>2</sub> + (Al) eutectic, resulting in an increase in microhardness. The increase in hardness of the composites was related to the amount of particles introduced. Sintering at 450 ℃ and the cooling method influenced the hardness and compressive strength of the composites, which were higher by 10% and 13%, respectively, compared to composites sintered at 400 ℃. Tribological tests showed that introducing more and more magnesium particles into the aluminum matrix, followed by reactive sintering, increased the wear resistance. On the other hand, the sintering temperature and cooling conditions had little effect on the wear resistance of the Al-Mg composites.</p> </abstract>

An efficient particulate photocatalyst for overall water splitting based on scandium and magnesium co-doped strontium titanate

A high photocatalytic performance for overall water splitting was demonstrated over a photocatalyst based on a magnesium and scandium co-doped strontium titanate particle composed of a cubic shape having a nanosized step structure on the edge of the particle.

Study on the characteristics parameters of magnesium dust explosion suppression by various inert gases

Alongside the extensive use of magnesium, dust explosion accidents have become increasingly frequent. Conducting research on suppressing magnesium dust explosions is of great significance for the healthy development of the magnesium industry. In this paper, the effects of four inert gases (CO2, N2, Ar, and He) on the explosion characteristics parameters of magnesium dust clouds with different concentrations were investigated using a closed explosion device. It was observed that at low volume fractions of inert gases in the explosion system, there were no significant differences in their effects on the explosion characteristics parameters and the combustion time of magnesium particles. In situations where there was a high level of oxygen, N2 was more effective than Ar in suppressing explosions. However, when the concentration of magnesium dust cloud was higher and the oxygen content was lower within the hybrids, N2 reacted with magnesium dust that was unable to react with oxygen. As a result, the explosion suppression effect gradually shifted from N2 being better than Ar to Ar being better than N2. Moreover, the differences in the effects of four inert gases on particle combustion time became increasingly prominent. However, in all operating conditions, CO2 demonstrated the most effective suppression of magnesium dust explosions, while He exhibited the least effective suppression effect. Furthermore, by employing a chemical reaction kinetics calculation model, it has been discovered that the content of inert gases significantly affected the combustion time and reaction mode of particle combustion, thereby causing variations in the propagation behavior of magnesium dust cloud flames.