Mn In Samples Research Articles

Microalloy Mg-based degradation implant for intra-osteal fixation

The bottleneck for Mg-based degradable implants lies in the mismatching relationship between mechanical properties and degradable rate, resulting in the rapid failure during the in-vivo degradable process and potential toxic role. Herein microalloy-conception has been involved to rectify the equilibrium effects among several aspects. Microstructure, mechanical properties, degradable properties and in-vitro/in-vivo biocompatibility properties of as-extruded pure Mg, Mg-0.15Ca, and Mg-0.15Ca-0.10Mn samples have been investigated. The results show that the Mg-0.15Ca-0.1Mn alloy exhibits a high yield strength (110 MPa) and a low degradable rate (0.82 mm/y). Attractively, the mechanical integrity has been remained in Mg-0.15Ca-0.1Mn alloy after 14 weeks in the rat femoral mode, and a homogenous degradable rate with 0.92 mm/y has been confirmed, which are far lower than those in-vitro values. Simultaneously, the low concentration of ions also reveals satisfactory biocompatibility equal to pure Mg, based on organ function and pathological morphology. Our findings reveal that microalloy paves a possible route to design high performance Mg-based intra-osteal fixation implants, resolving the contradictions among the degradable requirements under different body environments.

Synthesis, characterization, and performance evaluation of unsupported tetrametallic CoMoMnAl and CoMoZnAl catalysts for selective hydrodesulfurization (HDS)

New formulations of unsupported tetrametallic catalysts derived from layered double hydroxides (LDH) compounds were synthesized by a constant pH coprecipitation method, characterized, and evaluated in the selective hydrodesulfurization (HDS) of thiophene in the presence of cyclohexene. The layered double hydroxides were prepared using terephthalate (C8H8O2)2- as the interlayer anion with nominal aluminum molar fraction of 0.5, and nominal cobalt to MII (M = Zn or Mn) ratios of 0.2, 0.4 and 0.6. Molybdenum introduction in the LDH precursor was accomplished by an ion exchange process using the heptamolybdate anion. The calcined Mn samples showed a higher surface area than those obtained from Zn. The sulfidation was carried out in situ with a heating ramp up to 673 K and the catalysts were evaluated in a tubular flow reactor. The catalytic evaluation of Zn and Mn-based materials for simultaneous thiophene HDS and cyclohexene hydrogenation (HYD) was conducted at 573 K and 20 bar. The results show that the Zn-based unsupported catalysts synthesized here exhibited higher selectivity for the HDS reaction than an industrial one.

Chemical Imaging of Carbide Formation and Its Effect on Alcohol Selectivity in Fischer Tropsch Synthesis on Mn-Doped Co/TiO2 Pellets.

X-ray diffraction/scattering computed tomography (XRS-CT) was used to create two-dimensional images, with 20 μm resolution, of passivated Co/TiO2/Mn Fischer-Tropsch catalyst extrudates postreaction after 300 h on stream under industrially relevant conditions. This combination of scattering techniques provided insights into both the spatial variation of the different cobalt phases and the influence that increasing Mn loading has on this. It also demonstrated the presence of a wax coating throughout the extrudate and its capacity to preserve the Co/Mn species in their state in the reactor. Correlating these findings with catalytic performance highlights the crucial phases and active sites within Fischer-Tropsch catalysts required for understanding the tunability of the product distribution between saturated hydrocarbons or oxygenate and olefin products. In particular, a Mn loading of 3 wt % led to an optimum equilibrium between the amount of hexagonal close-packed Co and Co2C phases resulting in maximum oxygenate selectivity. XRS-CT revealed Co2C to be located on the extrudates' periphery, while metallic Co phases were more prevalent toward the center, possibly due to a lower [CO] ratio there. Reduction at 450 °C of a 10 wt % Mn sample resulted in MnTiO3 formation, which inhibited carbide formation and alcohol selectivity. It is suggested that small MnO particles promote Co carburization by decreasing the CO dissociation barrier, and the Co2C phase promotes CO nondissociative adsorption leading to increased oxygenate selectivity. This study highlights the influence of Mn on the catalyst structure and function and the importance of studying catalysts under industrially relevant reaction times.

Health Risk Assessment of Toxic Metal(loids) Consumed Through Plant-Based Anti-diabetic Therapeutics Collected in the Northern Divisional City of Rajshahi, Bangladesh.

The present study investigates human health risks upon consumption of herbal medicines in terms of ten toxic metalloids in 20 plant-based anti-diabetic therapeutics. The analysis of metalloids was determined by an atomic absorption spectrometer after microwave-assisted digestion. The computation of hazard quotients (HQ) and hazard indexes (HI) of metalloids leads to the assessment of non-carcinogenic health risks. Carcinogenic risk was assessed based on cancer slope factor (CSF) and chronic daily intake (CDI) values. Comparison with WHO regulatory cut-off points for each metalloid: seven samples for Mn, 12 samples for Hg, three samples for Cu, eight samples for Ni, four samples for Cd, two samples for Pb, one sample for Cr, and eight samples for Zn are unsafe to consume. Non-carcinogenic human health risk is predicted for Mn in seven samples, Fe in one sample, Hg in ten samples, Cu in three samples, Ni in one sample, and Pb in two samples. HI values greater than 1 predict non-carcinogenic health risk in thirteen samples. Incremental lifetime cancer risk (ILCR) remains for As (inorganic) in 12 samples, Cr (+ 6) in one sample, and Pb in no samples. To guarantee consumer safety, the implementation of strict monitoring is suggested.

Preparation of Nanosized Copper–Manganese Composite Oxides and Their Catalytic Performance in the Oxidation of Toluene

Nanosized Cu–Mn composite oxide catalysts were prepared from potassium permanganate, copper nitrate, n-butanol, and cetyltrimethylammonium bromide as a manganese source, copper source, reducing agent, and surfactant, respectively. The Cu[Formula: see text]–Mn sample possessed a small particle size (10–40[Formula: see text]nm) and a relatively high specific surface area ([Formula: see text]); its main components were Cu[Formula: see text]Mn[Formula: see text]O4 and Mn3O4. As a consequence, the Cu[Formula: see text]–Mn catalyst exhibited good catalytic activity in the oxidation of toluene. At a toluene concentration of 1000[Formula: see text]ppm and a space velocity of [Formula: see text], the [Formula: see text] and [Formula: see text] of the Cu[Formula: see text]–Mn catalyst toward toluene were 239[Formula: see text]C and 250[Formula: see text]C, respectively. Furthermore, even after 30[Formula: see text]h of operation at 275[Formula: see text]C, the conversion of toluene was 99% (at the space velocity of [Formula: see text]).

Enhanced strength, cytocompatibility, and corrosion resistance of biodegradable Zn-1.5Mg-0.5HA-xMn (x=1 and 1.5 wt%) composites for bone implant applications

Zn, a biodegradable metal, exhibits immense capability as a bioresorbable implant material because of its remarkable biocompatibility and stronger corrosion resistance than Mg. Nonetheless, Zn's limited mechanical strength and hardness have significantly hindered its widespread implementation. This study aimed to strengthen the mechanical, degradation resistance, and biocompatibility of zinc composites by rolling them and investigating the impact of Mn content on the material properties of Zn composites. The prepared hot rolled Zn-1.5Mg-0.5HA(hydroxyapatite)-1.5Mn (ZMR2) sample shows enhanced Ultimate tensile strength (UTS 209 MPa) and hardness (103 HV). In a PBS solution, the degradation rates of the hot-rolled sample show a consistent reduction as the content of Mn increases, reaching a rate of 0.032 mm/year. Furthermore, excellent hemocompatibility was observed for both the cast and rolled specimens. However, the rolled ZMR2 sample exhibited the lowest value (4.5 %) among the two. The cultured MG63 cells demonstrated high viability when exposed to diluted extracts (25 % and 50 % extract) of the HR ZMR2 sample from Day 1 to Day 5. In both cases, the viability exceeded 80 %, indicating the absence of any potential cytotoxic effects.

Environmental Assessment of Heavy Metal Pollution around Industrial Area in Southwestern, Nigeria

This study investigated heavy metal contamination around an industrial district in Obajana, Southwest Nigeria. The study region lies between latitudes 7°54′N to 7°56′N and longitudes 6°24′E to 6°27′E. Thirty samples each for groundwater and soil and twelve plant samples were collected from the study area. All samples were collected in triplicate. The physical and chemical parameters of the groundwater, soil, and plant samples were measured. The average pH level of the groundwater samples is 7.2 which falls within the Nigerian Standards for Drinking Water Quality (NSDWQ). The ranges of the other physical parameterssuch as electrical conductivity (EC), total dissolved solids (TDS) and total hardness (TH) are also within the acceptable limits. The mean concentrations of heavy metals in groundwater samples for Mn (0.020 mg/L), Zn (0.010 mg/L), Ni (0.010 mg/L), Cr (0.130 mg/L), Cu (0.020 mg/L), and Fe (0.090 mg/L) are within the allowable limit, with the exception of Pb (0.090 mg/L) that is above the recommended level. According to the index of geo-accumulation (Igeo), the soil and plant samples are not polluted with respect to the heavy metals tested. The analysis of the human risk assessment reveals that the values for the carcinogenic risk are within acceptable bounds; however, the values for the non-carcinogenic risk are substantially above the acceptable bounds. This demonstrates that non-carcinogenic health impacts are a threat to the broader population. This study suggests continuous monitoring of groundwater, soil, and plant in the study area.

Defects engineered ferroelectricity and electrocaloric effect in Pb0.7Ba0.3ZrO3 ceramics

Point defects play a versatile role in modulating ferroelectricity and piezoelectricity, however, the decisive role of point-defect concentration/species in controlling macroscopic performance remains unknown. In this work, defects are implanted by reduced atmosphere annealing and/or Mn doping in Pb0.7Ba0.3ZrO3 ceramics. i) defects induce lattice distortion, internal lattice strain and accordingly, phase structure is changed (Williamson-Hall analysis and Rietveld refinement); ii) ferroelectricity is enhanced for 0 MN and 1 MA sample with contribution of defect polarization (first-order reversal curves). iii) Joule heat is depressed as an enhanced resistivity by carrier annihilation/forming defect complex; iv) ECE behaves distinctly among 0 MN, 1 MA and 1 MH, respectively. 0 MN sample exhibits a ΔTmax of 0.39 K and 1 MA possesses a ΔTmax of 0.34 K. Interestingly, a broad temperature span with a low instability of ∼20 % within 288 K–423 K is obtained in 1 MH sample. This work not only provides a guideline for defects enhancing ferroelectricity and ECE, but also clarifies the reduction-resistant properties of (Pb, Ba)ZrO3 system that are suitable for constructing base-metal multilayer ceramic capacitors in solid-state cooling devices.

Towards sustainable electrochemistry: green synthesis and sintering aid modulations in the development of BaZr0.87Y0.1M0.03O3−δ (M = Mn, Co, and Fe) IT-SOFC electrolytes

In this study, BaZr0.87Y0.1M0.03O3−δ perovskite electrolytes with sintering aids (M = Mn, Co, and Fe) were synthesized by a sustainable approach using spinach powder as a chelating agent and then compared with chemically synthesized BaZr0.87Y0.1M0.03O3−δ (M = Mn, Co, and Fe) electrolytes for intermediate temperature SOFCs. This is the first example of such a sustainable synthesis of perovskite materials with sintering aids. Structural analysis revealed the presence of a cubic perovskite structure in BaZr0.87Y0.1M0.03O3−δ (M = Mn, Co, and Fe) samples synthesized by both green and conventional chemical methods. No significant secondary phases were observed in the samples synthesized by a sustainable approach. The observed phenomena of plane shift were because of the disparities between ionic radii of the dopants, impurities, and host materials. The surface morphology analysis revealed a denser microstructure for the electrolytes synthesized via green routes due to metallic impurities in the organic chelating agent. The absence of significant impurities was also observed by compositional analysis, while functional groups were identified through Fourier-transform infrared spectroscopy. Conductivity measurements showed that BaZr0.87Y0.1M0.03O3−δ (M = Mn, Co, and Fe) electrolytes synthesized by oxalic acid have higher conductivities compared to BaZr0.87Y0.1M0.03O3−δ (M = Mn, Co, and Fe) electrolytes synthesized by the green approach. The button cells employing BaZr0.87Y0.1Co0.03O3−δ electrolytes synthesized by the chemical and green routes achieved peak power densities 344 and 271 mW·cm−2 respectively, suggesting that the novel green route can be applied to synthesize SOFC perovskite materials with minimal environmental impact and without significantly compromising cell performance.

Evaluating the capacity of heavy metal pollution enrichment in green vegetation in the industrial zone, Northwest China

It focused on heavy metal pollution of green vegetation in Tuokexun County, Xinjiang Northwest China's suburban industrial area, using inductively coupled plasma emission spectrometer to analyze the samples for Mn, Ni, Zn, Cd, Hg, Pb, As, Cu, and Cr contents. The soil's heavy metal content in the study area indicated a minor level of pollution overall (P = 1.77), with the most severe contamination being Hg, which is more likely to be caused by human activities. Heavy metal elements in trees have the most stable composition in comparison to grass and shrubs, with varying concentrations across different vegetation. The concentrations of Mn, Cd and Hg were highest in the Haloxylon ammodendron, Ni in Morus alba, Pb, As and Cu in Nitraria tangutorums, and Cr in Phragmites australis. Heavy metal restoration is most effectively performed by shrubs, and there are disparities in heavy metal enrichment among various vegetation. No significant difference was found in heavy metal enrichment between the aboveground and underground parts of vegetation. Based on the average of the membership function, Tamarix exhibits the strongest ability to enrich heavy metals, while Nitraria tangutorum comes in second, and Cynanchum chinense R.Br. is the least effective among all plant species. Morus alba is recommended as the primary planting species in the area. Nitraria tangutorum and Haloxylon ammodendron have good potential for Cd and As restoration and can be used as supporting vegetation.

Identification of hub genes and their correlation with immune infiltrating cells in membranous nephropathy: an integrated bioinformatics analysis

BackgroundMembranous nephropathy (MN) is a chronic glomerular disease that leads to nephrotic syndrome in adults. The aim of this study was to identify novel biomarkers and immune-related mechanisms in the progression of MN through an integrated bioinformatics approach.MethodsThe microarray data were downloaded from the Gene Expression Omnibus (GEO) database. The differentially expressed genes (DEGs) between MN and normal samples were identified and analyzed by the Gene Ontology analysis, the Kyoto Encyclopedia of Genes and Genomes analysis and the Gene Set Enrichment Analysis (GSEA) enrichment. Hub The hub genes were screened and identified by the weighted gene co-expression network analysis (WGCNA) and the least absolute shrinkage and selection operator (LASSO) algorithm. The receiver operating characteristic (ROC) curves evaluated the diagnostic value of hub genes. The single-sample GSEA analyzed the infiltration degree of several immune cells and their correlation with the hub genes.ResultsWe identified a total of 574 DEGs. The enrichment analysis showed that metabolic and immune-related functions and pathways were significantly enriched. Four co-expression modules were obtained using WGCNA. The candidate signature genes were intersected with DEGs and then subjected to the LASSO analysis, obtaining a total of 6 hub genes. The ROC curves indicated that the hub genes were associated with a high diagnostic value. The CD4+ T cells, CD8+ T cells and B cells significantly infiltrated in MN samples and correlated with the hub genes.ConclusionsWe identified six hub genes (ZYX, CD151, N4BP2L2-IT2, TAPBP, FRAS1 and SCARNA9) as novel biomarkers for MN, providing potential targets for the diagnosis and treatment.

Fuzzy-Based Human Health Risk Assessment for Shallow Groundwater Well Users in Arid Regions

The conventional point-estimate human health risk assessment (HHRA) primarily uses average concentrations of a limited number of samples due to the high monitoring costs of heavy metals in groundwater. The results can be erroneous when concentrations significantly deviate from the average across the collected samples in an investigation region. The present research developed a hierarchical fuzzy-based HHRA (F-HHRA) framework to handle variations in limited data sets and subjectively established a broader range of risks for various exposure groups. Groundwater samples from 80 to 120 m deep in shallow wells were collected from agricultural farms along Wadi Rumah in the Qassim Region of Saudi Arabia. Laboratory testing found total dissolved solids much higher than the promulgated drinking water quality standards. As the aftertaste issue eliminated the raw water potability, the study considered dermal exposure for HHRA. The collected samples were tested for thirteen potential heavy metals (HMs), including barium (Ba), boron (B), cadmium (Cd), chromium (Cr), copper (Cu), iron (Fe), lead (Pb), lithium (Li), manganese (Mn), silver (Ag), strontium (Sr), thallium (TI), and zinc (Zn). Cu, Fe, Pb, Ag, and TI were lower than the detectable limit of the inductively coupled plasma mass spectrometry device. Concentrations of the remaining HMs in wastewater outfalls that were much less than the groundwater eradicated the impact of anthropogenic activities and affirmed natural contamination. Apart from 10% of the samples for Mn and 90% of the samples for Sr, all the other HMs remained within the desired maximum allowable concentrations. Point-estimate and fuzzy-based approaches yielded ‘low’ dermal non-cancer risk and cancer risk for all groups other than adults, where dermal cancer risk of Cr remained in the ‘acceptable’ (1 × 10−6 and 1 × 10−5) risk zone. Although dermal risk does not require controls, scenario analysis established the rationality of F-HHRA for more contaminated samples. The proposed hierarchical F-HHRA framework will facilitate the decision-makers in concerned agencies to plan risk mitigation strategies (household level and decentralized systems) for shallow well consumers in Saudi Arabia and other arid regions.

Assessment of Heavy Metal Pollution in Irrigation Water of Rajshahi City, Bangladesh

Heavy metal in irrigation water can be absorbed by crops, resulting in their accumulation in edible plant portions. These metals can be ingested through foods produced with contaminated water, which can result in organ damage, concerns with child development, neurological illnesses, and even cancer. This study, therefore, focuses on the estimation of Pb, Cr, Mn, and Cd in irrigation water along with their pollution assessments. Pb, Cr, Mn, and Cd concentrations were found in the range of 0.0211-0.2104, 0.00105-0.00937, 0.0913-0.3701, and 0.0004-0.0222 mg/L, respectively. This study found that 80% of samples for Mn and 55% for Cd exceeded the permissible limit recommended by the Food and Agricultural Organization. Pollution assessments were carried out using the enrichment factor, geoaccumulation index, contamination factor, and modified degree of contamination. This study also revealed that the geoaccumulation index and contamination factor indicated higher levels of Mn and Cd contamination. The government and organizations should establish stringent heavy metals regulations, regular monitoring, public awareness, and robust wastewater management to prevent contamination. However, due to limited metals and samples, further studies with a large number of heavy metals and samples are essential to a more profound understanding of sources, distribution, health impacts, and effective mitigation strategies.

Degraded creep resistance induced by static precipitation strengthening in high-pressure die casting Mg–Al–Sm alloy

Relationship between precipitation strengthening and creep resistance improvement has been an important topic for the widespread applications of magnesium alloys. Generally, static precipitation strengthening through thermal stable precipitates would generate satisfactory creep resistance. However, an opposite example is presented in this work and we propose that the size of precipitates plays a crucial role in controlling the operative creep mechanisms. In addition, the precipitate components along with their crystal structures in the crept Mg–4Al–3Sm–0.4Mn samples with/without pre-aging were thoroughly studied using Cs aberration-corrected high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM). Previous aging generates a large density of fine precipitates (< ∼5 nm) homogeneously distributing in Mg matrix and exhibiting satisfactory strengthening effect. However, the number density of precipitate strings consisting of several or even dozens of relatively coarse precipitates (∼10 nm) was significantly decreased at the same time. As revealed in this work, the relatively coarse particles in Mg matrix are much more efficient than the fine precipitates in promoting dislocation climb. Therefore, the rate-controlling mechanisms are transferred from dislocation climb to dislocation slip after previous aging, thus leading to degradation of creep resistance. Moreover, there are mainly five types of precipitates/clusters, namely β″-(Al, Mg)3Sm, Al5Sm3, ordered Al–Sm cluster, ordered Al–Mn cluster and ordered/unordered AlMnSm clusters. The crystal structures of the former two precipitates were discussed and the formation mechanisms of the precipitates/clusters were revealed.

Effect of seasonal temperature shifts on body homeostasis, biochemical parameters and chemical composition of green ormer (Haliotis tuberculata) in the Northern Adriatic.

Seasonal responses of green ormer in terms of antioxidant capacity and lipid peroxidation, proximate and fatty acid tissue composition, trace and macro elements concentrations over the seasons were studied in relation to temperature shifts in the Northern Adriatic Sea. Overall antioxidative defenses (SOD, TBARS, TAS, LDH) varied significantly (p<0.001) according to seasons (primarily spring and summer). The proportions of overall SFA were highest in summer. The proportions of MUFA increased in autumn, with significant differences between genders in spring and summer, and spring, summer and autumn for C18:1n7 and C20:4n6. The only fatty acid lacking significant variation between seasons was C22:5n3. Significant overall differences were observed in summer vs. winter samples for As, Ba, Co, Ni, Mn, Pb, Sb, and Se content in soft tissues, however, gender variations were not significant. The data obtained in the study are of utmost importance for the management of this under-investigated species.

A comparative study of magnetic, and magnetocaloric properties of different transition metal-doped La0.67Sr0.33AO3 (A: Mn, Co, Cr, and Fe) samples

A comparative study of magnetic, and magnetocaloric properties of different transition metal-doped La0.67Sr0.33AO3 (A: Mn, Co, Cr, and Fe) samples

Effect of Ni and Mn dopant on thermoelectric power generation performance of ZnO nanostructures synthesized via hydrothermal method

In this article, we have presented a low-cost hydrothermal approach to enhance the thermoelectric performance of ZnO nanostructures via modulation doping. For this purpose, we have prepared a series of pure and X:ZnO (X = Ni & Mn) samples. The Seebeck value of the Mn-doped samples possesses the maximum Seebeck coefficient of −36 μV/°C compared to the pure and Ni-doped samples (−22 μV/°C & −27 μV/°C) at room temperature. The highest value of the Seebeck coefficient for the Mn-doped samples is related to the formation of mid-gap energy band states due to the substitution of Mn2+ with Zn2+. These mid-band states induce an imbalance in the DOS, by producing a spin polarization effect that leads to a high Seebeck value. In terms of electrical conductivity, the Ni-doped ZnO sample exhibits the highest electrical conductivity of about 122 S/cm, due to the incorporation of Ni metal ions inside the ZnO matrix (confirmed by XRD) and leads to a high carrier concentration. However, the highest Seebeck value for the Mn-doped sample results in the maximum thermoelectric power factor ∼1.12 × 10−5 Wm−1C−2 at room temperature.

Synthesis of Mn2+ modified CdS nanoparticles and its application as catalyst in photodegradation of methyl red dye

Photocatalytic degradation of methyl red dye using Mn(5%) doped CdS nanoparticles was studied.Mn doped CdS nanoparticles was synthesized by microwave assisted solvo thermal method where the chemicals used wereCadmium Acetate [(CH3COO)2Cd, H2O], Manganese Chloride [MnCl2.2H2O] and Sodium Sulfide [Na2S.xH2O]. X-Ray diffraction(XRD) analysis was carried out in order to analyze the structural dimensions of the synthesized nanoparticles and the average crystallite size has been calculated at the full width half maximum (FWHM) of the diffraction peaks using Debye-Scherer equation and it was found to be around2.3nm. FTIR spectra analysis was done in order to analyze different functional and vibrational groups present in the as synthesized sample of Mn doped CdSnanoparticles.The morphology of sample wasstudied by scanning electron microscope. The aqueous solution of methyl red[C15H15N3O2] has been prepared and was mixed with the as synthesized Mn doped CdSnanoparticles and was exposed for photocatalytic degradation using 100 W bulb. UV-visible spectra of the light irradiated methyl red solutions were studied at different interval of time and no red shift was observed with increase of exposure time. The intensity of the absorption peak was also found to be reduced with the increasing time interval. The photo degradation of methyl red dye was observed up to 90% at the exposure time of 90 minutes.

Achieving ultra-high strength and ductility in Mg–9Al–1Zn–0.5Mn alloy via selective laser melting

Fabrication of the Mg–9Al–1Zn-0.5Mn alloy with excellent mechanical performance using selective laser melting (SLM) technology is quite difficult owing to the poor weldability and low boiling point. To address these challenges and seek the optimal processing parameters, response surface methodology was systematically utilized to determine the appropriate SLM parameter combinations. Mg–9Al–1Zn-0.5Mn sample with high relative density (99.5 ± 0.28%) and favorable mechanical properties (microhardness = 95.6 ± 5.28 HV0.1, UTS = 370.2 MPa and At = 10.4%) was achieved using SLM parameters (P = 120 W, v = 500 mm/s and h = 45 μm). Microstructure was primarily constituted by quantities of fine equiaxed grains (i.e., α-Mg phase) and a small amount of β-Al12Mg17 structures (i.e., 4.96 vol%). Samples was dominated by a random texture with numerous spherical β-Al12Mg17 ([21¯1¯0]α// [111]β), long lath-like β-Al12Mg17 ([21¯1¯0]α// [11¯5]β and [1¯011]α// [32¯1¯]β), and short rod-shaped Al8Mn5 nanoparticles. Benefiting from grain boundary strengthening, solid solution strengthening, and precipitation hardening of various nanoparticles (β-Al12Mg17 and Al8Mn5), high-performance Mg–9Al–1Zn-0.5Mn alloy biomedical implants can be fabricated. Precipitation hardening dominates the strengthening mechanism of the SLM Mg–9Al–1Zn-0.5Mn alloy.

Synthesis of Mn2+modified CdS nanoparticles and its application as catalyst in photodegradation of methyl red dye

Photocatalytic degradation of methyl red dye using Mn(5%) doped CdS nanoparticles was studied.Mn doped CdS nanoparticles was synthesized by microwave assisted solvo thermal method where the chemicals used wereCadmium Acetate [(CH3COO)2Cd, H2O], Manganese Chloride [MnCl2.2H2O] and Sodium Sulfide [Na2S.xH2O]. X-Ray diffraction(XRD) analysis was carried out in order to analyze the structural dimensions of the synthesized nanoparticles and the average crystallite size has been calculated at the full width half maximum (FWHM) of the diffraction peaks using Debye-Scherer equation and it was found to be around2.3nm. FTIR spectra analysis was done in order to analyze different functional and vibrational groups present in the as synthesized sample of Mn doped CdSnanoparticles.The morphology of sample wasstudied by scanning electron microscope. The aqueous solution of methyl red[C15H15N3O2] has been prepared and was mixed with the as synthesized Mn doped CdSnanoparticles and was exposed for photocatalytic degradation using 100 W bulb. UV-visible spectra of the light irradiated methyl red solutions were studied at different interval of time and no red shift was observed with increase of exposure time. The intensity of the absorption peak was also found to be reduced with the increasing time interval. The photo degradation of methyl red dye was observed up to 90% at the exposure time of 90 minutes.