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The fluctuation of material parameters and coupling effects of them have significant effects on cross-sectional deformation of rectangular tube in rotary draw bending process. So, in this research, a global sensitivity analysis (GSA) system was established based on the combination of Morris' GSA method and 3-D finite element method, and the reliability of the system is validated. Based on the system built, the sensitivity values of different material parameters combinations were analyzed. The results show that (i) the maximum cross-sectional deformation ratio decreases with the increase of Young's module E and strain hardening exponent n, while the effects of strength coefficient K, initial yield stress σS, and thickness anisotropy exponent γ on cross-sectional deformation are opposite to those of E and n, (ii) the groups which contain E and γ simultaneously show greater sensitivity and the effect of group only including E and γ on cross-sectional deformation is the most remarkable, while the most insensitive group in different combinations contains K, and (iii) mostly, the sensitivity values of coupling groups to cross-sectional deformation are larger than those of one-parameter groups.
The pitting corrosion resistance of AL-6XN PLUS™ superaustenitic stainless steel, 304L, 316L, and 317L austenitic stainless steels was investigated using the cyclic polarization technique. These materials were evaluated in the as received condition and heat-treated at temperatures between 500 °C and 900 °C for 72 h. A thermodynamic simulation was performed using the software Thermocalc® to predict possible deleterious phases in selected temperatures. The simulations have predicted the sigma phase in the selected temperature range. An aqueous solution of sulfuric acid and sodium chloride was used as electrolyte in the corrosion tests. The results showed that pitting corrosion was not observed on the samples of AL-6XN PLUS™ steel. The 304L steel suffered pitting corrosion. All the polarization curves of this steel showed hysteresis characteristics of pitting corrosion. The 316L and 317L steels were resistant to pitting corrosion, but susceptible to crevice corrosion.
We have reported the chemical blending carbonization method to obtain microporous carbon with high surface area for application as electrode materials in supercapacitors. Aliphatic dicarboxylic acids with different methylene numbers (n = 2, 4, 6, and 8) react with phenolic resin (PF) during curing process. Abundant micropores are created in the carbon matrix after the decomposition of grafted or blocked diacids at temperature higher than 400 °C. The specific surface area (SSA) of the carbonized blending system increases with the diacid chain length, but decreases after n > 4 of the chain length. The maximum SSA of the blending system is up to 605.9 m2/g, which increased approximately 68% compared to that of the neat carbonized PF. Electrochemical investigation indicates that the highest specific capacitances of the blending system reaches 175 F/g at a specific current of 0.1 A/g in 30 wt% KOH aqueous electrolyte. Furthermore, the capacitance maintenance achieves 82.8% as the current density enlarged 55 times.
From recent nanoindentation experiments, two types of pop-in modes have been identified: a single pop-in with a large displacement excursion and a number of pop-ins with comparable and small displacement excursions. Theoretical analyses are developed here to study the roles played by indenter tip radius, pre-existing defect density, heterogeneous nucleation source type, and lattice resistance on the pop-in modes. The evolution of dislocation structures in earlier pop-ins provides input to modeling a stochastic, heterogeneous mechanism that may be responsible for the subsequent pop-ins. It is found that when the first pop-in occurs near theoretical shear stress, the pop-in mode is determined by the lattice resistance and tip radius. When the first pop-in occurs at low shear stress, whether the successive pop-in mode occurs depends on how the heterogeneous dislocation nucleation source density increases as compared to the increase of the total dislocation density. The above transitions are found to correlate well with the ratio of indenter tip radius to the mean spacing of dislocation nucleation sources.
The α-aminonitrile, 2-morpholino-2-(3,4,5-trimethoxyphenyl)acetonitrile (C15H20N2O4), was prepared through a silica sulfuric acid-catalyzed Strecker reaction between 3,4,5-trimethoxybenzaldehyde, morpholine, and two different cyanide sources. Molecular characterization was performed by Fourier transform infrared spectroscopy, gas chromatography–mass spectrometry, (1H, 13C – mono and bidimensional) nuclear magnetic resonance; crystallographic characterization was completed by X-ray powder diffraction of polycrystalline samples. The title compounds crystallized in a monoclinic system and unit-cell parameters are reported [a = 13.904(2), b = 5.1696(6), c = 21.628(3) Å, β = 104.31(1)°, unit-cell volume V = 1506.3(3) Å3, Z = 4]. All measured lines were indexed with the P21/a (No. 14) space group.
Many technological applications of austenitic shape memory alloys (SMAs) involve cyclical mechanical loading and unloading in order to take advantage of pseudoelasticity. In this paper, we investigated the effect of mechanical bending of pseudoelastic NiTi SMA wires using high-energy synchrotron radiation X-ray diffraction (SR-XRD). Differential scanning calorimetry was performed to identify the phase transformation temperatures. Scanning electron microscopy images show that micro-cracks in compressive regions of the wire propagate with increasing bend angle, while tensile regions tend not to exhibit crack propagation. SR-XRD patterns were analyzed to study the phase transformation and investigate micromechanical properties. By observing the various diffraction peaks such as the austenite (200) and the martensite (${\bar 1}12$), (${\bar 1}03$), (${\bar 1}11$), and (101) planes, intensities and residual strain values exhibit strong anisotropy, depending upon whether the sample is in compression or tension during bending.
Zn–Ni alloy coatings were deposited on rolled copper foil via electro-brush plating with different micro-force. Surface morphologies, microhardness, roughness, and bending performance were characterized. Mechanisms and influences of electro–brush plating micro-force on coatings performances were investigated and revealed. With the increase of electro-brush plating micro-force, surface morphologies of coatings become smooth and dense, and the grain size was refined. Microhardness of coatings had a gradually increasing tendency when the increasing amplification was reduced. However, surface roughness of coatings as well as bending performance increased firstly and then decreased. The mechanisms of micro-force generation and action were explained by mechanics theory and principle model. Plastic deformation and work hardening are generated and performances are improved. Consequently, the performance of electro-brush plating coatings has a tight relevance with micro-force.
Ion-exchanged Aurivillius materials form perovskite nanosheet booklets wherein well-defined bi-periodic sheets, with ~11.5 Å thickness, exhibit extensive stacking disorder. The perovskite layer contents were defined initially using combined synchrotron X-ray and neutron Rietveld refinement of the parent Aurivillius structure. The structure of the subsequently ion-exchanged material, which is disordered in its stacking sequence, is analyzed using both pair distribution function (PDF) analysis and recursive method simulations of the scattered intensity. Combined X-ray and neutron PDF refinement of supercell stacking models demonstrates sensitivity of the PDF to both perpendicular and transverse stacking vector components. Further, hierarchical ensembles of stacking models weighted by a standard normal distribution are demonstrated to improve PDF fit over 1–25 Å. Recursive method simulations of the X-ray scattering profile demonstrate agreement between the real space stacking analysis and more conventional reciprocal space methods. The local structure of the perovskite sheet is demonstrated to relax only slightly from the Aurivillius structure after ion exchange.
Experimental X-ray powder diffraction data, unit-cell parameters, and space group for trelagliptin succinate, C18H20FN5O2•C4H6O4, are reported [a = 18.481(6), b = 8.120(4), c = 7.903(4) Å, α = 89.972(0)°, β = 97.722(4)°, γ = 90.120(0)°, unit-cell volume V = 1175.37 Å3, Z = 2, and space-group P1]. All measured lines were indexed and are consistent with the P1 space group. No detectable impurity was observed.