On Modeling Hydrogen-Induced Crack Propagation Under Sustained Load

The failure of hydrogen containment components is generally associated with subcritical cracking. Understanding subcritical crack growth behavior and its dependence on material and environmental variables can lead to methods for designing structural components in a hydrogen environment and will be beneficial in developing materials resistant to hydrogen embrittlement. In order to identify the issues underlying crack propagation and arrest, we present a model for hydrogen-induced stress-controlled crack propagation under sustained loading. The model is based on the assumptions that (I) hydrogen reduces the material fracture strength and (II) crack propagation takes place when the opening stress over the characteristic distance ahead of a crack tip is greater than the local fracture strength. The model is used in a finite-element simulation of crack propagation coupled with simultaneous hydrogen diffusion in a model material through nodal release. The numerical simulations show that the same physics, i.e., diffusion-controlled crack propagation, can explain the existence of both stages I and II in the velocity versus stress intensity factor (V–K) curve.     

On the environmental similitude for fracture in the SENT specimen and a cracked hydrogen gas pipeline

We investigate the use of laboratory fracture specimens to ascertain the resistance to hydrogen embrittlement of a hydrogen pipeline with an axial crack on the inner diameter (ID) surface. In particular, we study the interaction of hydrogen with material elastoplasticity in single edge notch tension (SENT) specimens loaded in hydrogen gas at a pressure of 15 MPa. We find that the transient and steady state hydrogen concentration fields in the neighborhood of the crack tip in the SENT specimen and the real-life pipeline are essentially the same. This environmental similitude warrants the use of the SENT specimen in a gaseous hydrogen environment to examine the compatibility of steel pipelines with hydrogen.     

Synthesis,characterisation and potential biomedical applications of magnetic core–shell structures: carbon‐, dextran‐, SiO2 ‐ and ZnO‐coated Fe3 O4 nanoparticles

Due to the strong effect of nanoparticles'' size and surface properties on cellular uptake and bio‐distribution, the selection of coating material for magnetic core–shell nanoparticles (CSNPs) is very important. In this study, the effects of four different biocompatible coating materials on the physical properties of Fe₃ O₄ (magnetite) nanoparticles (NPs) for different biomedical applications are investigated and compared. In this regard, magnetite NPs are prepared by a simple co‐precipitation method. Then, CSNPs including Fe₃ O₄ as a core and carbon, dextran, ZnO (zincite) and SiO₂ (silica) as different shells are synthesised using simple one‐ or two‐step methods. A comprehensive study is carried out on the prepared samples using X‐ray diffraction, vibrating sample magnetometry, transmission electron microscopy and Fourier transform infrared spectroscopy analyses. According to the authors'' findings, it is suggested that carbon‐ and dextran‐coated magnetite NPs with high M _s have great potential in the application of magnetic resonance imaging contrast agents. Moreover, silica‐coated magnetite NPs with high coercivity are potentially suitable candidates for hyperthermia and ZnO‐coated Fe₃ O₄ is potentially suitable for photothermal therapy.Inspec keywords: iron compounds, carbon, silicon compounds, zinc compounds, nanomedicine, biomedical materials, nanofabrication, nanoparticles, magnetic particles, coatings, X‐ray diffraction, magnetometry, transmission electron microscopy, Fourier transform spectra, infrared spectra, biomedical MRI, hyperthermia, radiation therapyOther keywords: biomedical applications, magnetic core‐shell nanoparticles, CSNP, cellular uptake, biodistribution, coating material, biocompatible coating materials, co‐precipitation, dextran, zincite, silica, X‐ray diffraction, vibrating sample magnetometry, transmission electron microscopy, Fourier transform infrared spectroscopy, magnetic resonance imaging contrast agents, hyperthermia, photothermal therapy, SiO₂ ‐Fe₃ O₄ , ZnO‐Fe₃ O₄      

Effect of Carbon Shell on the Structural and Magnetic Properties of Fe3O4 Superparamagnetic Nanoparticles

Carbon-encapsulated iron oxides (Fe₃O₄/C) with a core/shell structure have been successfully synthesized by using a simple two-step hydrothermal method at 180 ^°C. Fe₃O₄ core nanoparticles were prepared by coprecipitation under two conditions. Synthesized nanoparticles were characterized by transmission electron microscopy (TEM), vibrating sample magnetometer (VSM), X-ray diffraction (XRD), and Fourier transform infrared (FTIR) spectroscopy. TEM images and FTIR results prove that carbon coated iron oxide is formed and the estimated size for most of them is below 11 nm, which was consistent with the XRD result. The Williamson–Hall (W–H) method has been used to calculate crystallite sizes and lattice strain based on the peak broadening of the Fe₃O₄ and Fe₃O₄/C nanoparticles. The results of VSM imply that the Fe₃O₄ core and core–shell nanoparticles are superparamagnetic. The saturation magnetization of Fe₃O₄ and Fe₃O₄/C are 49 emu/gr and 40 emu/gr, respectively. The magnetic behaviors reveal that the amorphous carbon shell can decrease the saturation magnetization of Fe₃O₄ nanoparticles due to core–shell interface effects and shielding.     

Electric Field Effects on Spin Polarized Transport in FM/NMS and FM/NMS/FM Structures in Interaction Approximation

In this article, we have solved spin-dependent drift-diffusion equations analytically by considering a spin selective barrier between the magnet and semiconductor layer in interaction approximation and also taking into account the correlation and exchange effects. We have studied the electric field effects on the spin polarized transport in the ferromagnetic/nonmagnetic semiconductor (FM/NMS) and FM/NMS/FM structures in a degenerate regime. We have shown by increasing the conductivity of semiconductor up to ferromagnetic conductivity, semiconductor effective resistance becomes smaller and the spin injection efficiency will be increased. Also, the electric field enhances spin polarization density. Furthermore, in injection structures with interfacial barriers, the electric field enhances spin polarization considerably. In fact, the spin selective interfacial barrier acts as a spin filter, which permits electrons with a particular spin direction ↑(↓) pass through the interface. In addition, the calculated results in interacting approximation show that spin injection is increased. Finally, it is found that in FM/NMS/FM structures at low-field regime, the width of the semiconductor has the important role in spin transport.     

A novel ionic liquid/micro-volume back extraction procedure combined with flame atomic absorption spectrometry for determination of trace nickel in samples of nutritional interest

A simple, highly sensitive and environment-friendly method for the determination of trace amount of nickel ion in different matrices is proposed. In the preconcentration step, the nickel from 10 mL of an aqueous solution was extracted into 500 μL of ionic liquid, 1-butyl-3-methylimidazolium hexafluorophosphate [C₄MIM][PF₆], containing PAN as complexing agent. Subsequently, the PAN complex was back-extracted into 250 μL of nitric acid solution, and 100 μL of it was analyzed by flow injection flame atomic absorption spectrometry (FI-FAAS). The main parameter influencing the extraction and determination of nickel, such as pH, concentration of PAN, extraction time and temperature, ionic strength, and concentration of stripping acid solution, were optimized. An enhancement factor of 40.2 was achieved with 25 mL sample. The limit of detection (LOD) and quantification obtained under the optimum conditions were 12.5 and 41.0 μg L^?1, respectively. To validate the proposed methods two certified reference materials 681-I and BCR No. 288 were analyzed and the results were in good agreement with the certified values. The proposed method was successfully applied to determination of nickel in water samples, rice flour and black tea.     

The Relationship Between Crack-Tip Strain and Subcritical Cracking Thresholds for Steels in High-Pressure Hydrogen Gas

Threshold stress intensity factors were measured in high-pressure hydrogen gas for a variety of low alloy ferritic steels using both constant crack opening displacement and rising crack opening displacement procedures. Thresholds for crack extension under rising displacement, K _THi, for crack extension under constant displacement, $ K_{\text{THi}}^{*} $ , and for crack arrest under constant displacement K _THa, were identified. These values were not found to be equivalent, i.e. K _THi < K _THa <  $ K_{\text{THi}}^{*} $ . The hydrogen assisted fracture mechanism was determined to be strain controlled for all of the alloys in this study, and the micromechanics of strain controlled fracture are used to explain the observed disparities between the different threshold measurements. K _THa and K _THi differ because the strain singularity of a stationary crack is stronger than that of a propagating crack; K _THa must be larger than K _THi to achieve equivalent crack tip strain at the same distance from the crack tip. Hydrogen interacts with deformation mechanisms, enhancing strain localization and consequently altering both the nucleation and growth stages of strain controlled fracture mechanisms. The timing of load application and hydrogen exposure, i.e., sequential for constant displacement tests and concurrent for rising displacement tests, leads to differences in the strain history relative to the environmental exposure history and promotes the disparity between $ K_{\text{THi}}^{*} $ and K _THi. K _THi is the only conservative measurement of fracture threshold among the methods presented here.     

Preconcentration, speciation and determination of ultra trace amounts of mercury by modified octadecyl silica membrane disk/electron beam irradiation and cold vapor atomic absorption spectrometry

Mercury (II) and methyl mercury cations at the Sub-ppb level were adsorbed quantitatively from aqueous solution onto an octadecyl-bonded silica membrane disk modified by 2-[(2-mercaptophyenylimino)methyl] phenol (MPMP). The trapped mercury was then eluted with 3ml ethanol and Hg2+ ion was directly measured by cold vapor atomic absorption spectrometry, utilizing tin (II) chloride. Total mercury (Hgt) was determined after conversion of MeHg+ into Hg2+ ion by electron beam irradiation. A sample volume of 1500ml resulted in a preconcentration factor of 500 and the precision for a sampling volume of 500ml at a concentration of 2.5microgl(-1) (n=7) was 3.1%. The limit of detection of the proposed method is 3.8ngl(-1). The method was successfully applied to analysis of water samples, and the accuracy was assessed via recovery experiment.     

Performance Analysis of Neural Network Detectors in DS/CDMA Systems

In this paper, we consider neural networks as the detectors of signals of users in DS/CDMA systems. We apply multilayer perceptron neural network with back propagation learning algorithm in AWGN and multipath fading channels. Our analysis results in significant reduction in the receiver complexity over the previous studies. We compare the performance of neural network with the conventional and suboptimal detectors in AWGN channel and with the RAKE and single user lower bound receivers in fading channels. We also apply different criterion for training the network such as the decision based, fuzzy decision, discriminative learning, minimum classification, and entropy neural networks in AWGN channels and compare their performance. Further, we propose modified decision based network which improves the performance of the decision based network. A comparison between multilayer perceptron and Hopfield neural detectors is presented.