Phase Content Research Articles

Effect of Al or Cu Content on Microstructure and Mechanical Properties of Zn Alloys Fabricated Using Continuous Casting and Extrusion

The effect of Al or Cu content on the microstructure and mechanical properties of continuous casting and extrusion Zn alloys has been studied by a room temperature tensile test, X-ray diffraction, and scanning electron microscope. With the increase in Al content, the microstructure of continuous casting and extrusion Zn alloys slightly coarsens, and the lamellar eutectic structure increases. The changes in the above structural factors result in a slight decrease in strength and a significant increase in the elongation of Zn-Al alloys. The strength of Zn alloys increases as the Cu content increases due to the increased content and size of the second phase in the Zn alloys. This means that the mechanical properties of Zn alloys can be adjusted by a continuous casting and extrusion process, and the improvement of equipment capacity can improve the structure and morphology of the alloys.

GREEN HPLC DETERMINATION OF PHENYTOIN AND METHOD VALIDATION

Objective: In this study, the chromatographic behavior of the antiepileptic drug phenytoin was determined by the green HPLC method. The optimization of the developed method was based on the capacity factor values of phenytoin in varying water-ethanol binary mixtures and the ethanol concentration in the mobile phase where the compound was analyzed. Material and Method: Ethanol-water binary mixtures containing 35%, 40%, and 45% (v/v) ethanol were used in the optimization for the determination performed by the RPLC method. Retention times of the compound were determined with the Zorbax SB-CN (150x4.6 mm, 3.5 µm ID) column. Analyzes were performed at a constant flow rate (0.3 ml/min) and column temperature (37°C). The optimum condition for quantitative analysis was determined as an ethanol-water binary mixture containing 40% (v/v) ethanol with a pH of 6.5. Result and Discussion: In this study, the hydrophobicity of phenytoin was calculated using the logk-φ relationship. The optimum condition was determined using the obtained chromatographic data, and the quantitative determination of phenytoin in the commercial tablet formulation was made by the internal standard method. Under these conditions, excellent linearity (r>0.99) was obtained in the concentration range of 0.8-2.8 μg/ml. The detection limit of the developed method is 0.021 μg/ml; the limit of quantitation was calculated as 0.064 μg/ml. The recovery value of the method was determined as 99.61%. It was concluded that the parameters of precision, accuracy, and method robustness were appropriate for the validation procedures.

Microstructure, mechanical properties and cutting performance of CVD Ti(B,N) coatings

TiB0.19N1.06, TiB0.70N0.66, and TiB1.23N0.19 coatings were deposited on cemented carbide via the chemical vapor deposition (CVD) method based on the calculated phase diagrams of the Ti–B–N system. The microstructures, mechanical properties and cutting performances of the Ti(B,N) coatings were systematically studied via X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), nanoindentation, etc. The coating compositions obtained via thermodynamic calculations show the same trend as the experimental values. The XRD and selected area electron diffraction (SAED) results of the coatings reveal that the phase assemblages transform from a dominant cubic structure of TiB0.19N1.06 to a hybrid of cubic and hexagonal structure of TiB0.70N0.66 and finally to a dominant hexagonal structure of TiB1.23N0.19. According to the XPS results, the TiB0.19N1.06 and TiB0.70N0.66 coatings consist of the crystalline phases TiN and TiB2 as well as amorphous BN and TiB, and the TiB1.23N0.19 coating mainly consists of the crystalline phases TiB2 and TiN. The hardness values of the TiB0.19N1.06, TiB0.70N0.66, and TiB1.23N0.19 coatings are 33.6, 35.1, and 39.1 GPa, respectively. The content of amorphous phase in the Ti(B,N) coatings decreases while the hardness increases as the B content increases and N content decreases. The TiB0.19N1.06 coating exhibits a composite structure of nanocrystallite embedded in amorphous matrix. The TiB1.23N0.19 coated tool prepared in this study demonstrates excellent performance in milling titanium alloy TC18 with a long cutting life up to 56.1 min, an increase of ∼9 % and ∼28 % compared to the TiB1.98 coated tool and commercial grade deposited with CVD TiB2 coating, respectively.

The effect of chromium on the corrosive performance of novel high manganese steel frogs in a simulated industrial atmosphere

Abstract The corrosion behavior of three novel high manganese steel frogs with different Cr contents in a simulated industrial corrosive atmospheric environment is studied through the corrosion weight gain, x-ray diffraction (XRD), scanning electron microscopy (SEM), x-ray photoelectron spectroscopy (XPS), and electrochemical testing. The results indicate that the content of Cr in the steel affects the phase composition, density, and electrochemical stability of the rust layer. For instance, as the Cr content increases, the content of the amorphous phase in the rust layer continuously increases while that of γ-FeOOH decreases, leading to enhanced density and electrochemical stability of the rust layer. The study reveals that Cr exists in the rust layer in the form of Cr2O3 and Cr(OH)3, providing nucleation cores to nanoscale colloidal rust particles. Consequently, a higher Cr content leads to more nucleation cores, which improves the density of the rust layer and enhances the corrosion resistance of the novel high manganese steel frogs in industrial corrosive atmospheric environments.

Targeted screening and profiling of massive components of colistimethate sodium by two-dimensional-liquid chromatography-mass spectrometry based on self-constructed compound database

In-depth study of the components of polymyxins is the key to controlling the quality of this class of antibiotics. Similarities and variations of components present significant analytical challenges. A two-dimensional (2D) liquid chromatography-mass spectrometric (LC-MS) method was established for screening and comprehensive profiling of compositions of the antibiotic colistimethate sodium (CMS). A high concentration of phosphate buffer mobile phase was used in the first-dimensional LC system to get the components well separated. For efficient and high-accuracy screening of CMS, a targeted method based on a self-constructed high resolution mass spectrum database of CMS components was established. The database was built based on the commercial MassHunter Personal Compound Database and Library (PCDL) software and its accuracy of the compound matching result was verified with 6 known components before being applied to genuine sample screening. On this basis, the unknown peaks in the CMS chromatograms were deduced and assigned. The molecular formula, group composition and origins of a total of 99 compounds, of which the combined area percentage accounted for more than 95% of CMS components, were deduced by this 2D-LC-MS method combined with the MassHunter PCDL. This profiling method was highly efficient and could distinguish hundreds of components within 3 h, providing reliable results for quality control of this kind of complex drugs.

Efficient reclamation of phosphorus from wetland biomass waste via liquid-recirculated hydrothermal carbonization and precipitation

Hydrothermal carbonization (HTC) for the recovery of phosphorus (P) from biomass wastes has attracted considerable attention, while migration of P to the liquid phase greatly weakened P recovery efficiency and elevated the environmental risk. Therefore, a systematic scheme was proposed in this work to accomplish the complete reclamation of P from wetland plant (Ceratophyllum demersum) through coupling liquid-recirculated HTC mediated by H2O or H2SO4 with precipitation, and the migration and speciation of P during this process was determined by P K-edge X-ray absorption near edge structure, 31P nuclear magnetic resonance, and the modified sequential extraction. The P concentration in the liquid phase increased with the recirculation of HTC process water, and reached up to 550.6 mg L-1. >98.1 % of P in the recirculated liquid products was recovered in the forms of hydroxyapatite and struvite with the HTC mediums of H2O and H2SO4, respectively, without the addition of exogenous metals. In addition to the production of P compounds, P-enriched hydrochar was simultaneously obtained during this process. The HTC medium and liquid recirculation had profound impact on the hydrochar characteristics and the transformation of P. Hydroxyapatite and magnesium phosphate were the dominant P species in the hydrochars derived from H2O-mediated HTC, while FePO4 and other Ca-P species [Ca3(PO4)2 and Ca(H2PO4)2] dominated the P compounds in the H2SO4-mediated hydrochar. These results suggest that coupling liquid-recirculated HTC and precipitation could be a promising strategy for P reclamation, which could provide new insights into the P recovery from biomass waste.

Enhancement of redox cycling stability of Ni/GDC cermets for intermediate-temperature SOFC anodes through Ge incorporation in the ceramic phase

In this study, Ge4+ was incorporated into the ceramic matrix of nickel-based anode materials, synthesizing anode materials NiO-Gd0.1Ce0.9-xGexO1.95 (x = 0.01, 0.04, 0.07) and NiO-Ce0.9Gd0.1O2–δ. Corresponding anode support samples were also prepared, designated as A-CGDC, A-C1Ge, A-C4Ge, and A-C7Ge. Additionally, single cell samples using the newly co-doped anode materials were prepared, identified as C-CGDC, C-C1Ge, C-C4Ge, and C-C7Ge. The research indicates that after doping the ceramic phase framework with Ge4+, these composite anode materials exhibit the potential to withstand more redox cycles than C-CGDC without catastrophic mechanical structural damage or degradation in electrochemical performance. Particularly, after incorporating 7mol% Ge4+ into the ceramic backbone, the issue of 86 % strain accumulation in the anode support was mitigated. Additionally, the ion doping ratio is closely linked to the stability of the single cell samples, with the A-C7Ge sample able to withstand up to 11 extreme recycling sessions at 700 °C without complete structural failure, improving structural stability by approximately 57 % compared to A-C1Ge. In terms of electrochemical output performance, the impedance of C-C1Ge prior to complete failure was nearly double that before oxidation-reduction, with a maximum power density reduction of about 26.47 %. As the co-doping concentration in the ceramic phase reached 7mol%, the impedance increase during single cell cycle testing was about four times smaller, with C-C7Ge 's impedance before mechanical failure only 37 % higher than before cycling, and a reduction in maximum power density of just 11.11 %. Moreover, during consecutive cycling tests, the average damage to the open-circuit voltage was only 0.02V, showing almost no negative impact from the cycling operations, and it maintained efficient output performance after multiple cycles. Therefore, the newly synthesized nickel-based anode materials, modified via co-doping methods within the ceramic phase, can be considered as potential composite anode materials for intermediate-temperature solid oxide fuel cells.

Sequencing-Dependent Impact of Carbon Coating on Microstructure Evolution and Electrochemical Performance of Pre-lithiated SiO Anodes: Enhanced Efficiency and Stability via Pre-Coating Strategy.

Silicon monoxide (SiO) has attracted considerable interest as anode material for lithium-ion batteries (LIBs). However, their poor initial Coulombic efficiency (ICE) and conductivity limit large-scale applications. Prelithiation and carbon-coating are common and effective strategies in industry for enhancing the electrochemical performance of SiO. However, the involved heat-treatment processes inevitably lead to coarsening of active silicon phases, posing a significant challenge in industrial applications. Herein, the differences in microstructures and electrochemical performances between prelithiated SiO with a pre-coated carbon layer (SiO@C@PLi) and SiO subjected to carbon-coating after prelithiation (SiO@PLi@C) are investigated. A preliminary carbon layer on the surface of SiO before prelithiation is found that can suppress active Si phase coarsening effectively and regulate the post-prelithiation phase content. The strategic optimization of the sequence whereprelithiation and carbon-coating processes of SiO exert a critical influence on its regulation of microstructure and electrochemical performances. As a result, SiO@C@PLi exhibits a higher ICE of 88.0%, better cycling performance and lower electrode expansion than SiO@PLi@C. The pouch-type full-cell tests demonstrate that SiO@C@PLi/Graphite||NCM811 delivers a superior capacity retention of 91% after 500 cycles. This work provides invaluable insights into industrial productions of SiO anodes through optimizing the microstructure of SiO in prelithiation and carbon-coating processes.

Dual-energy computed tomography for predicting cervical lymph node metastasis in laryngeal squamous cell carcinoma

Rationale and objectivesWe constructed a dual-energy computed tomography (DECT)-based model to assess cervical lymph node metastasis (LNM) in patients with laryngeal squamous cell carcinoma (LSCC). Materials and methodsWe retrospectively analysed 164 patients with LSCC who underwent preoperative DECT from May 2019 to May 2023. The patients were randomly divided into training (n = 115) and validation (n = 49) cohorts. Quantitative DECT parameters of the primary tumours and their clinical characteristics were collected. A logistic regression model was used to determine independent predictors of LNM, and a nomogram was constructed along with a corresponding online model. Model performance was assessed using the area under the curve (AUC) and the calibration curve, and the clinical value was evaluated using decision curve analysis (DCA). ResultsIn total, 64/164 (39.0 %) patients with LSCC had cervical LNM. Independent predictors of LNM included normalized iodine concentration in the arterial phase (odds ratio [OR]: 8.332, 95 % confidence interval [CI]: 2.813–24.678, P < 0.001), normalized effective atomic number in the arterial phase (OR: 5.518, 95 % CI: 1.095–27.818, P = 0.002), clinical T3-4 stage (OR: 5.684, 95 % CI: 1.701–18.989, P = 0.005), and poor histological grade (OR: 5.011, 95 % CI: 1.003–25.026, P = 0.049). These predictors were incorporated into the DECT-based nomogram and the corresponding online model, showing good calibration and favourable performance (training AUC: 0.910, validation AUC: 0.918). The DCA indicated a significant clinical benefit of the nomogram for estimating LNM. ConclusionsDECT parameters may be useful independent predictors of LNM in patients with LSCC, and a DECT-based nomogram may be helpful in clinical decision-making.

A Limited Evaluation of the Applicability of NACE MR0175/ISO 15156 H2S Limits to Supercritical CO2 Pipelines

In an earlier paper one of the authors raised the question of whether the hydrogen sulfide (H2S) partial pressure threshold of 0.05 psia (0.3 kPa) for cracking of steels from sulfide stress cracking is pertinent to dense phase carbon dioxide (CO2) systems in which there is no free gas phase. This paper presents a limited test of the pertinence of this threshold value in Supercritical CO2. Autoclave tests of four-point bend beam specimens of API 5L Grade X80 line pipe steel at 0.05 psia (0.3 kPa) and 0.20 psia (1.38 kPa) H2S were performed and the samples were examined after testing for cracking. In addition, the test conditions were modeled with the OLI Studio software to determine the H2S fugacities and H2S concentrations in the brine phase. No cracking was found after 30 d of exposure.

Behavior of free-standing atmospheric plasma sprayed Al2O3–Cr2O3 solid solution-based coatings under cyclic heating at 1000 °C

This paper investigates the cyclic heating behavior of free-standing atmospheric plasma sprayed Al2O3 - Cr2O3 coatings containing a solid-solution phase. The coatings are deposited on steels by spraying mechanically blended Al2O3 - Cr2O3 powder mixture with variable Cr2O3 content (2–6 wt%) in the feedstock. The tests are performed up to 50 cycles at 1000 °C temperature in a muffle furnace in a normal atmosphere. After each cycle, the weight gain of the coatings is measured, and the oxidation rate constant (Kp) for each material is estimated. The microstructure and phases of the coatings are studied by using scanning electron microscopy (SEM) and X-ray diffractometry (XRD) techniques respectively. The porosity and crack length are estimated by image analysis (Image J) technique. The hardness of the coatings is measured by Vickers microhardness tester. After 50 cycles, all the free-standing coatings are found to be intact without fragmentation. At higher cycles, the Al2O3 - Cr2O3 coatings form α-Al2O3 and (Al0.9Cr0.1)2O3 solid-solution phase only. The Al2O3 - Cr2O3 coatings gain much less weight than the pure Al2O3 coating due to the major presence of oxidation resistant α-Al2O3 phase in the former. However, among the Al2O3 - Cr2O3 coatings with an increase in Cr2O3 content, the Kp value tends to increase due to the high presence of metastable (Al1.8Cr0.05)2O3 solid-solution phase. On the other hand, the (AlxCr1-x)2O3 phase helps to reduce crack formation due to its high fracture toughness properties. With the highest amount of solid-solution phase content, the Al2O3-4 wt% Cr2O3 coating shows the highest fracture toughness among all. The micro-porosity of the coatings is increased with an increase in the heating cycle, and the coating hardness is reduced accordingly.

Mechanical properties and corrosion resistance improvement of TiAlSnMo alloys via Mo addition

In this paper, Ti-5Al-2.5Sn-xMo (TASxM, x = 0,5,10,15 wt%) alloys were designed and prepared. Phase compositon and microstructure analysis results indicate that the addition of Mo reduces the phase transition point of TASxM alloys, stabilizes more β phase to room temperature, and refines the α grains. The strength of the TASxM alloys exhibits a positive correlation with the increasing Mo content within 10 wt%, and the highest ultimate tensile strength (UTS) can be obtained in TAS10M (1260 MPa), which can be primarily attributed to the synergistic effects of phase transition, solid solution strengthening, and fine grain strengthening. Interestingly, the UTS of TAS15M unexpectedly decreases to 724 MPa, which is strongly influenced by the altered slip system numbers resulting from the β/α phase ratio. Even more intriguing is the observation of stress-induced martensitic transformation in the deformed TAS15M alloy, often resulting in a substantial influence on elongation. The corrosion resistance of the TASxM alloy has also been investigated through electrochemical experiments. The findings reveal that the corrosion resistance of the TASxM alloy is enhanced with the elevation of Mo content, peaking at TAS15M. This improved resistance is attributed to the augmented β phase content and the formation of protective MoO2 and MoO3 oxide films on the surface of alloy.

Characterization of bulk interior and fusion crust of Calama 009 L6 ordinary chondrite

AbstractFragment of Calama 009 L6 ordinary chondrite recovered in the Atacama Desert was chosen for a complex study of the bulk interior and the fusion crust by scanning electron microscopy (SEM) with energy‐dispersive spectroscopy (EDS), X‐ray diffraction (XRD), magnetization measurements, and Mössbauer spectroscopy. SEM demonstrated the presence of Fe‐Ni‐Co grains, troilite and chromite inclusions in both the bulk interior and the fusion crust as well as many veins with ferric compound. EDS showed variations in the Ni concentration within the metal grains and within one metal phase in the grain. XRD revealed some differences in the contents of various phases in the bulk interior and in the fusion crust. XRD indicated the presence of magnesioferrite in the fusion crust as well as the formation of goethite nanoparticles with the mean size of 9 nm in both the bulk interior and the fusion crust. Magnetization measurements demonstrated the ferrimagnetic–paramagnetic phase transition in chromite at 44 K and low values of the saturation magnetization moments (6.46 and 3.26 emu g−1 at 100 K) for the bulk interior and the fusion crust, respectively, due to the lack of Fe‐Ni‐Co alloy as a result of weathering. The Mössbauer spectra of the bulk interior and the fusion crust showed some differences in the number and relative areas of spectral components. The revealing of the Mössbauer spectral components related to 57Fe in the M1 and M2 sites in olivine and orthopyroxene as well as determining the Fe2+ occupations of these sites from XRD permitted us to estimate the temperature of equilibrium cation distribution for these silicates which are (i) 662 K (XRD) and 706 K (Mössbauer spectroscopy) for olivine and (ii) 893 K (XRD) and 910 K (Mössbauer spectroscopy) for orthopyroxene.

Simulation of anaerobic biodegradation process in a tubular bioreactor with a biofilm layer: Steady-state and unsteady-state conditions

In this paper, anaerobic biodegradation process in a tubular bioreactor with an inner biofilm layer for steady-state and unsteady-state conditions are simulated. The effects of various parameters including bioreactor diameter, fraction of active biomass transferred to liquid phase, and residence time of the liquid on bioreactor performance are examined. Simulations indicate that decreasing diameter of bioreactor leads to increasing degree of conversion of the substrate in liquid phase and decreasing dimensionless concentration of the substrate in biofilm. With an increase in the fraction of active biomass transferred to liquid, substrate concentrations in liquid and biofilm slightly vary. Increased residence time of the liquid phase results in the degree of conversion of substrate goes up, but substrate concentration in biofilm lowers a little. In addition, it is found that biomass concentration of liquid phase is boosted with decreased bioreactor diameter and increased residence time of liquid. A proportional-integral controller is designed and the tuned parameters of KP=−0.131 and KI=0.02 are obtained using genetic algorithm. It is observed that controller regulate well the degree of conversion of the substrate within 120 s for both servo and regulatory modes.

Two deep learning methods in comparison to characterize droplet sizes in emulsification flow processes

AbstractFor reliable supervision in multiphase processes, the droplet size represents a critical quality attribute and needs to be monitored. A promising approach is the use of smart image flow sensors since optical measurement is the most commonly used technique for droplet size distribution determination. For this, two different AI-based object detection methods, Mask RCNN and YOLOv4, are compared regarding their accuracy and their applicability to an emulsification flow process. Iterative optimization steps, including data diversification and adaption of training parameters, enable the models to achieve robust detection performance across varying image qualities and compositions. YOLOv4 shows better detection performances and more accurate results which leads to a wider application window than Mask RCNN in determining droplet sizes in emulsification processes. The final droplet detection model YOLOv4 with Hough Circle (HC) for feature extraction determines reliable droplet sizes across diverse datasets of liquid-liquid flow systems (disperse phase content 1–15 vol.-%, droplet size range 5–150 μm). Evaluating the adjustment of Confidence Scores (CS) ensures statistical representation of even smaller droplets. The droplet detection performance of the final YOLOv4 model is compared with a manual image processing method to validate the model in general as well as its accuracy and reliability. Since YOLOv4 in combination with Hough Circle (HC) shows an accurate and robust detection and size determination, it is applicable for online monitoring and characterization of various liquid-liquid flow processes. Graphical abstract

Effects of Cr and Mo content on the microstructure and properties of Fe-based amorphous composite coatings by laser cladding

In this study, we successfully produced Fe-based amorphous composite coatings on the surface of 45 steel using laser cladding technology, and the impact of the relative content of Cr and Mo elements on the microstructure, hardness, and wear resistance of composite coatings has been investigated. The results show that the microstructure of the coating changes from dendrite to amorphous nanocrystalline when the content of Cr and Mo is 20 and 15 wt. %, respectively. However, when the Mo element continues to be added, elemental segregation will be caused, resulting in a large number of brittle Fe–Cr–Mo intermetallic compounds and MoSi2 ceramic phases in the coating. Therefore, the appropriate element ratio can not only increase the amorphous phase content in the coating but also prevent elemental segregation. Among the three types of amorphous composite coatings studied, the Fe45Cr20Mo15B10Si10 (wt. %) composite coating exhibited the most favorable performance, primarily due to its highest amorphous content (43.33%). Through the interaction of the amorphous phase, α-Fe, Fe–Cr solid solution, and a small proportion of intermetallic compounds, this coating achieved a hardness of 1282.8 HV0.2, approximately five times that of the 45 steel substrate, and demonstrated superior wear resistance.

Effect of different Zn/Mg ratios on the uniformity of 7185+TiB2/TiC aluminum alloy thick plates

Three types of 7185+TiB2/TiC aluminum matrix composites with different Zn/Mg ratios were prepared in this work through a water-cooled copper casting process. The effects of Zn/Mg ratio on the microstructure and mechanical properties of 20-mm-thick composites were studied by optical microscopy, electron back scattering diffraction, transmission electron microscopy, and tensile mechanical testing. The results showed that the addition of appropriate TiB2/TiC particles refined the as-cast microstructure of the alloy, and with a decrease in Zn/Mg ratio, the grain size distribution became more uniform, the crystalline phase content gradually increased, and the uniformity of the alloy increased. After aging, as the Zn/Mg ratio decreased, the size of the precipitated phase decreased, and the strengthening effect of the alloy improved. The tensile strengths of the surface layer, 1/4 layer, and center position of the A3 alloy were 558, 568, and 572 MPa, respectively. The strength difference among the different thickness layers was the smallest, and the elongation rate was greater than 12%, resulting in the best uniformity.

Steady State and Time-Resolved Fluorescence Spectroscopy of Cinchonine Dication in Sodium Dodecylsulphate Micellar System.

This paper reports the influence of surface charge of the micelles on to the photophysical properties of a cinchonine dication (C2+) fluorophore in anionic, sodium dodecylsulphate (SDS), surfactant at premicellar, micellar and post-micellar concentrations in aqueous phase at room temperature. The magnitude of edge excitation red shift (EERS) in the fluorescence maximum of C2+ in bulk water solution is 1897cm- 1 whereas, in the case of SDS it is observed to be 1984cm- 1. The fluorescence decay curve of C2+ fits with multi exponential functions in the micellar system. The increase in lifetime of C2+ in SDS has been attributed to the increase in radiative rate due to the incorporation of C2+ at the micelle -water interface. The value of dynamic quenching constant determined is 16.9 M- 1. The location of the probe molecule in micellar systems has been justified by a variety of spectral parameters such as dielectric constant, ET (30), viscosity, EERS, average fluorescence decay time, radiative and non-radiative rate constants. All experimental results suggest that the C2+ molecule binds strongly with the SDS micelles and resides at micellar-water interface. The binding constant (Kb) calculated (3.85 × 105 M- 1) for C2+ in SDS revealed that the electrostatic forces mediate charge probe-micelle association.

Influence of heat treatment on the microstructure evolution and corrosion performance of biodegradable Zn-Mg alloys

Zinc and zinc-based alloys have garnered increasing attention as biodegradable materials due to their excellent mechanical properties, lower degradation rates compared to magnesium, and favorable biocompatibility. This study investigates the impact of homogenization treatment on the microstructure and corrosion behavior of Zn-Mg alloys using scanning electron microscopy, X-ray diffraction, hardness testing, and accelerated corrosion immersion tests. The results reveal that homogenization treatment induces the fusion of eutectic cells within the alloys, causing significant morphological alternations in the eutectic structure and varying proportions of the Mg2Zn11 phase, These changes notably affect material properties. The raised content of Mg2Zn11 phase in the eutectic structure correlates with higher hardness but reduced corrosion resistance, whereas the reduced Mg2Zn11 phase content leads to enhanced corrosion resistance. Furthermore, in-situ corrosion observations demonstrate that corrosion initiates at the eutectic phase, with corrosion pits forming due to the ion release as corrosion progresses, leading to gradual enlargement of the corrosion pits. In summary, this study provides comprehensive insights into the microstructural changes in Zn-Mg alloys and their impact on corrosion resistance, offering valuable references for their engineering applications.

Influence of Menstrual Cycle and Oral Contraceptive Phases on Bone (re)modelling Markers in Response to Interval Running

To explore how sex hormone fluctuations may affect bone metabolism, this study aimed to examine P1NP and β-CTX-1 concentrations across the menstrual and oral contraceptive (OC) cycle phases in response to running. 17β-oestradiol, progesterone, P1NP and β-CTX-1 were analysed pre- and post-exercise in eight eumenorrheic females in the early-follicular, late-follicular, and mid-luteal phases, while 8 OC users were evaluated during the withdrawal and active pill-taking phases. The running protocol consisted of 8 × 3min treadmill runs at 85% of maximal aerobic speed. 17β-oestradiol concentrations (pg·ml−1) were lower in early-follicular (47.22 ± 39.75) compared to late-follicular (304.95 ± 235.85;p = < 0.001) and mid-luteal phase (165.56 ± 80.6;p = 0.003) and higher in withdrawal (46.51 ± 44.09) compared to active pill-taking phase (10.88 ± 11.24;p < 0.001). Progesterone (ng·ml−1) was higher in mid-luteal (13.214 ± 4.926) compared to early-follicular (0.521 ± 0.365; p < 0.001) and late-follicular phase (1.677 ± 2.586;p < 0.001). In eumenorrheic females, P1NP concentrations (ng·ml−1) were higher in late-follicular (69.97 ± 17.84) compared to early-follicular (60.96 ± 16.64;p = 0.006;) and mid-luteal phase (59.122 ± 11.77;p = 0.002). β-CTX-1 concentrations (ng·ml−1) were lower in mid-luteal (0.376 ± 0.098) compared to late-follicular (0.496 ± 0.166; p = 0.001) and early-follicular phase (0.452 ± 0.148; p = 0.039). OC users showed higher post-exercise P1NP concentrations in withdrawal phase (61.75 ± 8.32) compared to post-exercise in active pill-taking phase (45.45 ± 6;p < 0.001). Comparing hormonal profiles, post-exercise P1NP concentrations were higher in early-follicular (66.91 ± 16.26;p < 0.001), late-follicular (80.66 ± 16.35;p < 0.001) and mid-luteal phases (64.57 ± 9.68;p = 0.002) to active pill-taking phase. These findings underscore the importance of studying exercising females with different ovarian hormone profiles, as changes in sex hormone concentrations affect bone metabolism in response to running, showing a higher post-exercise P1NP concentrations in all menstrual cycle phases compared with active pill-taking phase of the OC cycle.