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Zr-based bulk metallic glasses are promising engineering materials due to their good glass-forming abilities and unique combination of good strength (∼1.9 GPa) and medium stiffness. In this study, the corrosion behaviors of Zr–Co–Al–Ag BMGs, with silver content from 0 to 11 at.%, in NaCl and H2SO4 solutions were investigated. The corrosion resistance increased when the silver content increased. The oxidation behaviors of Zr–Co–Al–Ag BMGs were also studied. The oxidation kinetics of all the samples obeyed a two-stage parabolic rate law, which consisted of an initial transient oxidation followed by a steady-state oxidation stage. The addition of Ag was found to reduce the oxidation resistance of Zr–Co–Al–Ag BMGs. Some white nodules, possibly cobalt oxide, were observed when the Zr–Co–Al–Ag BMG with 8 at.% Ag was oxidized at high temperature.
In this paper, we report the structural, electrical, and magnetic properties of polycrystalline La0.85–xSmxNa0.15MnO3 (x = 0.05, 0.1, 0.15) manganites. Rietveld refinement of x-ray data infers that doped manganite compounds possess a rhombohedrally distorted structure (space group $R\bar 3C$). Both lattice parameter and unit cell volume decrease and a systematic change in both Mn–O–Mn bond angle and tolerance factor is observed with Sm content. Resistivity measurements discern metal–insulator transition (TP). For x = 0.15 sample, a double metal–insulator transition with a single ferromagnetic transition is depicted. All samples exhibit extrinsic magnetoresistance (MR) effect. A large value of MR of 65% (253 K, 8 T) is associated with grain and grain boundary formation. The highest low-field MR of 23% (12 K, 2 T) and 35.2% (23 K, 2 T) for x = 0.05 and 0.1 is observed. The electronic and magnetic inhomogeneities induced by Sm and nonmagnetic metal Na phases account for MR properties.
The CeCo3Ni2 compound was synthesized by arc melting under argon atmosphere. High-quality powder X-ray diffraction (XRD) data of CeCo3Ni2 have been collected using a Rigaku SmartLab X-ray powder diffractometer. The refinement of the XRD pattern for the CeCo3Ni2 compound shows that the CeCo3Ni2 is a hexagonal structure, space group P6/mmm (No.191) with a = b = 4.9081(2) Å, c = 4.0034(2) Å, V = 83.52 Å3, Z = 1, and ρx = 8.6347 g cm−3. The Smith–Snyder FOM F30 = 112.7(0.0089, 30) and the intensity ratio RIR = 0.48.
The mechanical and thermal behavior of nanoglasses (NGs) were studied with a focus on the effect of the microstructure. The thermal expansion was measured to track changes in excess free volume during heating. It was found that the excess free volume, which is initially more dominant in the interphase region between the denser amorphous particles, is partially lost as well as redistributed during annealing. This relaxation during heating causes the nanoglass to behave like a melt-spun ribbon after heating while remaining amorphous. Nanomechanical tests were used to probe the local incipient plasticity and the influence of the interphase region. This interphase appears to affect the mechanical response of the NGs by inhibiting the propagation of shear bands and thus offers a novel approach for the introduction of plasticity in bulk metallic glasses. The results suggest that the NGs consist of two distinct amorphous phases with different glass transition temperatures.
This article presents a new multiscale modeling approach proposed to predict the impact response of a biomedical niobium–zirconium alloy by incorporating both geometric and microstructural aspects. Specifically, the roles of both anisotropy and geometry-based distribution of stresses and strains upon loading were successfully taken into account by incorporating a proper multiaxial material flow rule obtained from crystal plasticity simulations into the finite element (FE) analysis. The simulation results demonstrate that the current approach, which defines a hardening rule based on the location-dependent equivalent stresses and strains, yields more reliable results as compared with the classical FE approach, where the hardening rule is based on the experimental uniaxial deformation response of the material. This emphasizes the need for proper coupling of crystal plasticity and FE analysis for the sake of reliable predictions, and the approach presented herein constitutes an efficient guideline for the design process of dental and orthopedic implants that are subject to impact loading in service.
The infrared emissivity properties of carbon fibers with different treatments were investigated in the wave length range 6–15 μm from 1273 to 1873 K. The heat treatment affected the infrared emissivity of carbon fibers through the microstructure evolution. The Raman investigation about the microstructure indicated that the increase of the graphitization degree in carbon fibers degenerated the infrared emissivity of carbon fibers, especially under high temperatures. For the coated carbon fibers, the infrared emissivity properties were decreased for carbon fibers coated pyrolytic carbon (PyC) due to the lamellar structure of PyC and increased for carbon fibers deposited carbon nanotubes (CNTs) owing to the skeleton-like structure of CNTs. The study also illustrated that the PyC coating thickness from 0.5 to 1.0 μm had few effects on the infrared emissivity properties of carbon fibers.
Multilayer stereo micro/nanometer-sized porous surface structures were prepared by selective chemical etching of biphasic calcium phosphate (BCP) scaffolds with hydroxyapatite (HAP)/β-tricalcium phosphate (β-TCP) weight ratios of 90/10, 80/20, 70/30, 60/40, and 50/50 in phosphoric acid solution. The porous surface structures revealed periodic fluctuations in the observed heights of micro/nanometer-sized needles. And the average height increased from 0.59 ± 0.02 to 12.09 ± 0.03 μm when the β-TCP content in BCP scaffolds rose from 10 to 50%. In vivo cell tests using MG-63 cells (belonging to the human osteosarcoma cell line) revealed that micro/nanometer-sized pores on the scaffold surface could provide location for cell adhesion and migration and facilitate the formation of gap junction between cells. The BCP scaffold with 40% β-TCP exhibited the optimal surface structure for cell seeding and growth due to the largest number of micro/nanometer-sized pores on the surface. However, excessive β-TCP led to the damage of micro/nanometer-sized porous surface structure, which further impeded the cell interaction.
A simple hydrothermal route to the eulytite phase of bismuth germanium oxide (E-BGO: Bi4(GeO4)3) that required no post-processing has been developed. The E-BGO material was isolated from a mixture of bismuth nitrate pentahydrate and a slight excess of germanium oxide in water under hydrothermal conditions (185 °C for 24 h). The resultant materials were characterized by powder x-ray diffraction, scanning electron microscopy, transmission electron microscopy, and luminescence measurements to verify the particle's phase (eulytite), morphology, size, and response to a variety of excitation energy sources, respectively. Photoluminescence spectroscopic response from E-BGO pellets indicated that the samples exhibited a strong emission peak consistent with an x-ray induced luminescence of a E-BGO single crystal (500 nm excited at 285 nm). Cathodoluminescent properties of the E-BGO displayed a broadband spectrum with a maximum at 487 nm. The growth process was consistent with a standard Oswald ripening and LaMer growth processes.
Synchrotron X-ray diffraction images are increasingly used to characterize crystallographic preferred orientation distributions (texture) of fine-grained polyphase materials. Diffraction images can be analyzed quantitatively with the Rietveld method as implemented in the software package Materials Analysis Using Diffraction. Here we describe the analysis procedure for diffraction images collected with high energy X-rays for a complex, multiphase shale, and for those collected in situ in diamond anvil cells at high pressure and anisotropic stress.
The dependence of polymer properties on their processing history can be used advantageously. Polyethylene terephthalate (PET), a semi-crystalline polymer, exhibits a microstructure reliant on process and thermal history. PET undergoes strain-induced crystallization, making it sensitive to mechanical stretching. As the level of crystallinity in PET governs its mechanical behavior, it is necessary to quantify the effect of crystallinity and molecular orientation for efficient use. The present research is focused on an approach that will aid in correlating the stretch ratio of PET films to the percent crystallinity and mechanical properties. PET films with different local stretch ratios were obtained through bi-axially stretching injection-molded cylinders of increasing thickness and weight. Percent crystallinity of the PET films with different stretch ratios was measured using X-ray diffraction. Film samples were marked with respect to the stretch directions for measuring their longitudinal (primary stretch direction) and transverse mechanical properties. Local molecular orientation in the form of pole figures was mapped using the (100) plane corresponding to the PET lattice. This will help in linking the physical sample directions and processing to the molecular orientation. Associating the mechanical properties with molecular alignment helps in designing production processes that realize the material's structural potential.
This paper summarizes an oral presentation of the same title presented at the occasion of recognizing the “The 100th Anniversary of X-ray Spectroscopy” at DXC 2013. It gives an overview of the development in electronics with focus on (mainly) energy-dispersive X-ray detectors and related data processing. Naturally this has its origin in the early transistors and the first semiconductor junction detectors of the late 1940s. It was followed by refinement of semiconductor detector technology in general and particularly by the invention of Li-drifting and employment of low-noise field effect transistors until such devices matured sufficiently to be marketed by the late 1960s. Further improvement followed in resolution, speed, operability at room temperature, and development of junction arrays with imaging capabilities. An important aspect is the development of related software requiring affordable laboratory computers, programming languages, and databases of fundamental parameters. Today x-ray fluorescence analysis (and not only the energy-dispersive variant) is widely employed as an analytical tool for the traditional technical and industrial applications but notably also, at an expanding rate as well as variety, in other fields including environmental, medical, archaeological, space, arts, and many more.
Calcium monoaluminate is the main phase in calcium aluminate cements and participates in the hydration, forming calcium aluminate hydrates. The amount of incorporation of foreign ions influences the hydration behaviour. Strontium aluminate is an important phase in producing phosphorescent materials when doped with rare-earth elements (REE) such as Eu, Dy, and La. These monoaluminates occur in different forms. Monocalcium aluminate forms a monoclinic and an orthorhombic modification, whereas monostrontium aluminate forms a monoclinic low-temperature and a hexagonal high-temperature form. Monoclinic calcium monoaluminate and monoclinic strontium aluminate form a partial solid-solution series. The hydration behaviour of different solid solutions was also investigated using calorimetry. The newly formed strontium aluminate hydrates could be identified while similar strontium aluminate hydrates are formed. Solid solutions of strontium- and calcium-aluminate hydrates will be investigated.
Al6061 and AZ31 plates were processed using accumulative roll bonding (ARB) method up to two passes to produce laminated composites. The sandwich stacks of Al6061/AZ31/Al6061 were held at 450 °C for 10 min in a cubical furnace and rolled together with reduction of 50% in one pass. The microstructural investigations were done using optical and scanning electron microscopes. The structures of the interface, mechanical and drop impact properties of the laminated composites after the first and second passes were investigated and compared with Al6061 and AZ31 alloy plates. It was found that Al6061 improved the elongation to failure property of AZ31 after the first pass of ARB process and the drop impact properties of AZ31 after the first and second passes. However, elongation to failure magnitude with the uniaxial tensile loading decreased with increase in the number of passes due to the formation of brittle intermetallic between the Al6061/AZ31 nonuniform interfaces.