Experimental phase equilibria study and thermodynamic modelling of the PbO-“FeO”-SiO2-ZnO,PbO-“FeO”-SiO2-Al2O3 and PbO-“FeO”-SiO2-MgO systems in equilibrium with metallic Pb and Fe

Phase equilibria of the PbO-“FeO”-SiO₂-ZnO, PbO-“FeO”-SiO₂-Al₂O₃ and PbO-“FeO”-SiO₂-MgO slags with liquid Pb metal, solid or liquid Fe metal and solid oxides (cristobalite and tridymite SiO₂, willemite (Zn,Fe)₂SiO₄, wustite (Fe,Al)O_1+x, spinel (Fe,Al)₃O₄, olivine Fe₂SiO₄, corundum (Al,Fe)₂O₃, mullite Al₆Si₂O₁₃ and pyroxene (Mg,Fe)SiO₃) were investigated at 1125–1670 °C. These conditions correspond to the minimum solubility of PbO in slag in presence of Pb and Fe metals at reducing conditions and represent the limit of lead smelting and slag cleaning process. High-temperature equilibration on silica, corundum or iron foil substrates, followed by quenching and direct measurement of Pb, Fe, Si, Zn, Al and Mg concentrations in the liquid and solid phases with the electron probe X-ray microanalysis (EPMA) was used. Present data can be used to improve the thermodynamic models for all phases in this system.     

Red-shift and improved afterglow of Sr3Al2-xBxO5Cl2:Eu2+, Dy3+ phosphors via a cation substitution strategy

Sr₃Al_2-xB_xO₅Cl₂:Eu²⁺, Dy³⁺ (x = 0, 0.2, 0.4) long persistent phosphors were prepared via solid-state process. The pristine Sr₃Al₂O₅Cl₂:Eu²⁺, Dy³⁺ phosphor exhibits orange/red broad band emission around 609 nm, which can be attributed to the electric radiation transitions 4f⁶5 d¹→4f⁷ of Eu²⁺. Upon the same excitation, the B³⁺-doped Sr₃Al_2-xB_xO₅Cl₂:Eu²⁺, Dy³⁺ phosphors display red-shift from 609 nm to 625 nm with increasing B³⁺ concentrations. The XRD patterns show that Al³⁺ can be replaced by B³⁺ in the host lattice at the tetrahedral site, which causes lattice contraction and crystal field enhancement, and thereafter achieves the red-shift on the emission spectrum. The XPS investigation provides direct evidence of the dominant 2-valent europium in the phosphor, which can be ascribed for the broad band emission of the prepared phosphors. The afterglow of all phosphors show standard double exponential decay behavior, and the afterglow of Sr₃Al₂O₅Cl₂:Eu²⁺, Dy³⁺is rather weak, while the sample co-doped with B³⁺shows longer and stronger afterglow, as confirmed after the curve simulation. The analysis of thermally stimulated luminescence showed that, when B³⁺ is introduced, a much deeper trap is created, and the density of the electron trap is also significantly increased. As a result, B³⁺ ions caused redshift and enhanced afterglow for the Sr₃Al_2-xB_xO₅Cl₂:Eu²⁺, Dy³⁺ phosphor.     

Microstructure-abrasive wear correlation of in situ ZA27/TiC composites

Abrasive wear is a complex surface degradation process driven by various factors such as microstructure, the mechanical properties of the target material, the abrasive, loading conditions, and the surrounding environment. In this study, in situ TiC reinforced Zinc Aluminum alloy composites were prepared through a liquid metallurgy route and the synergistic effect of applied load, sliding speed, abrasive grit size and TiC content on the high-stress abrasive wear response were investigated. The test materials' wear response was established by characterising wear surfaces, sub-surfaces, debris particles, and an abrasive medium. The study suggests that the wear resistance of the specimens decreases with an increase in the applied load, and the composite reinforced with 10 wt % of TiC shows superior wear behaviour among all the test materials. The study also points out that the ZA-27 alloy reinforced with in situ TiC can be a suitable replacement of the conventionally used materials for automotive applications.     

The effect of synthesis conditions on the phase composition and structure of thorium bearing murataite ceramics

Samples of thorium-bearing ceramic with a target composition (wt%) 5 Al₂O₃, 10 CaO, 55 TiO₂, 10 MnO, 5 Fe₂O₃, 5 ZrO₂, 10 ThO₂ were produced by melting in glassy carbon crucibles in a resistive furnace and by cold crucible inductive melting (CCIM) at a vibration power of 10 kW and operation frequency of 5.28 MHz. All the samples contained 85–95 vol% murataite polytypes with 5- (5C), 8- (8C), and 3-fold (3C) elementary fluorite unit cell composing core, intermediate zone and rim of the grains, respectively, and minor crichtonite, perovskite, pyrochlore, rutile, etc. A feature of the ceramics obtained by melting in glassy carbon crucibles is formation of Fe (II) titanate whereas the inductive-melted ceramics contained traces of vitreous phase due to melt contamination with a cold crucible putty material. Melting rate in the cold crucible of up to 350 kg/(m² × h) has been achieved. The ceramics obtained have excellent chemical durability.     

不同改良措施对排土场土壤微形态影响的试验研究

以铁矿排土场废石土为研究对象,自制模型试验装置,设计4种基质改良方法,开展SEM检测实验,并应用IPP软件对SEM照片进行定量化分析,研究在不同改良措施下对铁矿排土场土壤微结构的影响。结果表明：单施3%有机肥土壤孔隙度为16%,与对照组排土场原矿土相比增加了60%。复合施用3%有机肥、掺拌30%的黄土的处理孔隙度达到最大33%。单施3%有机肥、5%有机肥对土壤大团聚体含量皆有显著的促进作用,复合施有机肥、掺拌黄土的处理与单施有机肥的处理对比,土壤大团聚体含量增加并不显著。各改良措施的MWD与FMD均随着土壤中大团聚体的含量增加而增加。     

Fabrication of highly sensitive MnO2/F-MWCNT/Ta hybrid nanocomposite sensor with different MnO2 overlayer thickness for H2O2 detection

In this work, we report the development of MnO₂/F-MWCNT/Ta hybrid nanocomposite sensor with different MnO₂ overlayer thickness for the detection of H₂O₂ in real samples. A novel two-step process using e-beam evaporation and spray pyrolysis deposition was adopted for the synthesis of hybrid MnO₂/F-MWCNT/Ta electrodes. SE morphology revealed smaller-sized, compact grains of MnO₂ infiltrated on the outermost walls of MWCNTs. Raman analysis confirmed the existence of carbon nanotubes with abundant structural defects of MnO₂ in the composite. The cyclic voltammetry results displayed a high peak current and narrowed over potential towards the reduction of H₂O₂. The sensor displayed a fast response (<5?s), wide linear range (2–1510?μM) and a low limit of detection (0.04?μM) with significant anti-interfering properties, promising for the development of highly sensitive and reproducible biosensors. The three dimensional nanocomposite sensor also exhibited good recovery (> 98%), thus providing a favourable tool for analysis of H₂O₂ in milk samples.     

Effects of three types of modified atmospheric packaging on the physicochemical properties of selected glutinous rice

The effect of modified atmospheric packaging (MAP) on the physicochemical properties of selected glutinous (Thadokkham-8 and Thadokkham-11) rice was studied and compared with a non-glutinous rice (Doongara). The freshly harvested/milled grains were packed in four different MAP conditions viz. control, vacuum, CO₂ and N₂ for 12 months at room temperature (23 ± 1 °C). Gas (N₂ or CO₂) was flushed in aluminum bags at the pressure of 300 kPa for 3 s and subsequently hermetically sealed. Vacuum packaging was done at −100 kPa. Results showed that ageing induced changes in the starch granules were less prominent in vacuum and/or MAP samples using CO₂ or N₂. Surface analysis showed that control storage significantly reduced the percentage of lipids and increased the percentage of proteins on the surface in all selected varieties. N₂ and CO₂ storage of TDK8 and DG slowed down the shift of properties of macromolecules and maintained the surface starch/proteins/lipids ratios during 6 months of storage. Moreover, the grains stored in vacuum maintained the lipids with lower proportion of proteins exposed to the surface after cooking. N₂ and CO₂ induced increase in pasting temperature but significant reduction in final viscosity when compared to control. The findings correlated well with thermal analysis. The in situ Thermal Mechanical Compression Test (TMCT) device cooking and texture analysis revealed that modified storage slightly slowed the ageing induced changes in the cooking quality and stickiness of glutinous rice. Among all storage conditions used vacuum was relatively the best to maintain the quality of the grain.     

The control of paracetamol particle size and surface morphology through crystallisation in a spray dryer

The parameters governing the crystallisation of paracetamol using various conventional techniques has been extensively studied, however the factors influencing the drug crystallisation using spray drying is not as well understood. The aim of this work was to investigate the crystallisation of an active pharmaceutical ingredient through evaporative crystallisation using a spray dryer to study the physicochemical properties of the drug and to use semi-empirical equations to gain insight into the morphology and particle size of the dried powder. Paracetamol solutions were spray dried at various inlet temperatures ranging from 60 °C to 120 °C and also from a series of inlet feed solvent compositions ranging from 50/50% v/v ethanol/water to 100% ethanol and solid-state characterisation was done. The size and morphology of the dried materials were altered with a change in spray drying parameters, with an increase in inlet temperature leading to an increase in particle Sauter mean diameter (from 3.0 to 4.4 µm) and a decrease in the particle size with an increase in ethanol concentration in the feed (from 4.6 to 4.4 µm) as a result of changes in particle density and atomised droplet size. The morphology of the dried particles consisted of agglomerates of individual crystallites bound together into larger semi-spherical agglomerates with a higher tendency for particles having crystalline ridges to form at higher ethanol concentrations of the feed.     

选区激光熔化工艺参数对气雾化316L不锈钢粉末成形制品性能的影响

本研究系统考察了激光功率和扫描速度对316L不锈钢粉末选区激光熔化工艺成形熔道、制品微观组织及力学性能的影响,并分析了各类缺陷的形成原因。研究结果表明:在低激光功率和高扫描速度条件下,熔道中出现了大量球状颗粒,这些颗粒之间的空隙恶化了下一层粉末的熔化条件,这正是成形制品中熔道分布混乱以及孔洞、裂纹产生的根本原因,进而导致成形制品力学性能降低;在高激光功率和低扫描速度条件下,熔池快速升温/冷却的热应力作用增强,使得成形制品的熔道交界处也存在孔洞和裂纹等缺陷。在本研究实验条件下,激光功率为350 W,扫描速度为1750 mm/s时,SLM成形制品的力学性能最为优异,其中抗拉强度为731 MPa、屈服强度为638 MPa、断后伸长率为40.0%,致密度为96.27%。     

Experimental studies and thermodynamic assessment of the Ba-Mo-O system by the CALPHAD method

Thermodynamic measurements on BaMoO₄, BaMoO₃ and BaMo₃O₁₀ are reported, that served as input for the development of a thermodynamic model of the Ba-Mo-O system using the CALPHAD methodology. The valence states of molybdenum in BaMoO₄ and BaMoO₃ were confirmed to be VI and IV, respectively, from X-ray Absorption Near Edge Structure Spectroscopy measurements at the Mo K-edge. The heat capacity at low temperatures of these compounds was obtained from thermal-relaxation calorimetry. Phase equilibrium data in the BaMoO₄-MoO₃ section were also measured, and the transition enthalpy associated with the peritectic decomposition of BaMo₃O₁₀ was determined using Differential Scanning Calorimetry. The developed thermodynamic model used the compound energy formalism for intermediate compounds, and an ionic two-sublattice model for the liquid phase. The optimized Gibbs energies were assessed with respect to the known thermodynamic and phase equilibrium data. A good agreement is generally obtained, but a number of ill-defined data were also identified.