Search

This paper presents results about the influence of the selective laser melting (SLM) process parameters on a FeCr4Mo1V1W8C1 (wt%) alloy regarding microstructure and mechanical behavior. Tailored parameter variation studies were performed to obtain crack-free and highly dense SLM parts. The microstructure was studied using scanning electron microscopy, X-ray diffraction, Auger electron spectroscopy, and scanning transmission electron microscopy. Additionally, the mechanical properties were investigated by compression and tensile tests. The obtained microstructure is composed of complex nanoscale carbides, retained austenite, and martensite. Caused by the fast directional cooling during SLM, a completely dendritic solidification aligned in building direction occurs. Non-equilibrium segregation leads to an orderly phase arrangement of complex carbides at the boundary of the dendrites surrounded by retained austenite and martensite in the center of the dendrites. A strong work hardening behavior was observed, based on an austenite-to-martensite phase transformation (TRIP effect). This effect accounts for the outstanding mechanical properties such as compression strength of 6000 MPa, a 0.2% tensile yield strength of 560 MPa, and an ultimate tensile strength of over 1000 MPa. These findings reveal that SLM is advantageous for the processing of ultra-high-strength FeCrMoVWC tool steel. [ABSTRACT FROM AUTHOR]

Natural fibers are particularly interesting from a materials point of view since their morphology has been tailored to enable a wide range of macroscopic level functions and mechanical properties. In this paper, we focus on mussel byssal threads which possess a morphology specifically designed to provide a hysteretic yet resilient large strain deformation behavior. X-ray diffraction studies have shown that numerous natural fibers have a multi-domain architecture composed of folded modules which are linked together in series along a macromolecular chain. This microstructure leads to a strong rate and temperature dependent mechanical behavior and one which exhibits a stretch-induced softening of the mechanical response as a result of the underlying morphology evolving with imposed stretched. This paper addresses the development of a constitutive model for the stress–strain behavior of the distal portion of mussel byssal threads based on the underlying protein network structure and its morphology evolving with imposed stretched. The model will be shown to capture the major features of the stress–strain behavior, including the highly nonlinear stress–strain behavior, and its dependence on strain rate and stretch-induced softening. [ABSTRACT FROM AUTHOR]

Polymer processing generally plays a crucial role in determining the development of microstructure in the fabricated product. In this paper, isotactic polypropylene (iPP) containing 0.1 wt% β-nucleating agent was extruded via a slit die and immediately melt-stretched upon various stretching rates (SR) at the die exit. The microstructure of β-nucleated iPP samples was investigated using two-dimensional wide-angle X-ray diffraction and small-angle X-ray scatterings (2D-WAXD/SAXS) measurements. It is observed that, no matter what SR is, lamellar branching of β-form crystal is formed in melt-stretched samples, which is scarcely reported in open literatures. A method is proposed to calculate the crystallinity of daughter lamellae in β-crystal ( X). It is found that X decreases with increasing SR, indicating that lamellar branching of β-form crystal is restrained by higher SR. Such case should be attributed to the denser-oriented structures (e.g., shish) induced by higher SR, leaving a confined space between adjacent-oriented structures for the growth of daughter lamellae. [ABSTRACT FROM AUTHOR]

In this paper, rapid solidified MgZnY (at.%) alloy powders produced by an inert gas atomizer were consolidated using a severe plastic deformation technique of high pressure torsion (HPT) at room temperature and 373 K. The behavior of powder consolidation, matrix microstructural evolution, and mechanical properties of the powders and compacts were investigated using X-ray diffraction, scanning electron microscopy, transmission electron microscopy, microhardness, and tensile testing. As the HPT processing temperature increases, the powders are more plastically deformed due to decreased deformation resistance, grain boundaries are more in equilibrium, powder bonding is enhanced due to increased interparticle diffusion, hence, tensile ductility and strength increases. On the other hand, hardness decreases with the increased processing temperature, due to less dislocation density. [ABSTRACT FROM AUTHOR]

We report in this paper on microstructural, optical and photocatalytic properties of single-phase indium orthovanadates, as a function of doping at lattice sites. The UV-visible spectra of these samples exhibited intense UV-region bands at 250 and 350 nm, besides broad absorption band in visible region (350-700 nm). The wavelength at absorption edge and the intensity of visible absorption showed considerable increase on doping of an impurity, particularly at V or O lattice sites. Also, the samples gave rise to blue-green photoluminescence emission, with overriding bands at ca. 420, 450, 460 and 485 nm, on excitation at 240-420 nm wavelengths. The intensity of these fluorescence bands varied with excitation wavelength and impurity content of a sample. In deviation with several earlier studies, only oxygen and no hydrogen were produced during photocatalytic splitting of water, in the experiments conducted under visible light (>395 nm) and at a pH of ~6.5. The O yield depended on the dispersed metal co-catalyst, impurity content and the addition of methanol as sacrificial reagent. On the other hand, small quantities of hydrogen and no oxygen were evolved on UV-irradiation of pure water using metal/InVO. These results are ascribed to flat band potentials and the doping-induced inter-band donor and acceptor charge trapping states of InVO, the presence of which is revealed by XRD, luminescence and XPS studies. Our study also confirms that the onset of absorption edge may not necessarily correspond to band-to-band energy gap of a semiconducting material. This accounts for some anomalous band gap energies reported earlier for InVO. [ABSTRACT FROM AUTHOR]

A study of the structural characteristics of the composites [Pb(Fe0.5Nb0.5)O3(PFN)] x -[Cr0.75Fe1.25O3(CRFO)]100− x ( x = 0 (CRFO100), 10, 50, 90, 100) was performed in this work. The compounds PFN100 and CRFO100 were prepared by conventional solid-state method and investigated by X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), and 57Fe Mössbauer Spectroscopy techniques. The X-ray analysis shows that PFN100 is tetragonal and the CRFO100 phase has a trigonal symmetry. The refinement of all the composites was also performed and discussed in this paper. The Mössbauer spectrum for the composite samples shows a paramagnetic doublet and a sextet probably assigned to a magnetic phase associated to Fe+3. For the sample PFN100, only a magnetic field of 49.5 T (isomer shift (δ) = 0.21 mm/s) was detected. For the composite sample, the δ and Δ are typical of Fe ions at sites of octahedral coordination. [ABSTRACT FROM AUTHOR]

Gd3+ was chosen as a substitute for Bi3+ in BiNbO4 ceramics, and the substitution effects on the sintering performance and microwave dielectric properties were studied in this paper. The high temperature triclinic phase was observed only in the Bi0.98Gd0.02NbO4 ceramics when sintered at 920 °C. Both bulk densities and dielectric constant (εr) increased with the sintering temperature, while decreased with the Gd content. The quality factor ( Q) exhibited a correlation to the Gd content and the microstructures of Bi1− x Gd x NbO4 ceramics. At the sintering temperature of 900 °C, Bi0.992Gd0.008NbO4 ceramics exhibited microwave dielectric properties of εr ∼ 43.87, Q × f ∼ 16,852 GHz (at 4.3 GHz), and its temperature coefficient of resonant frequency (τf) was found to be near-to-zero. [ABSTRACT FROM AUTHOR]