A kinetic model involving oxidation and volatilization in SiC-B4C-xAl2O3 ceramics system

In this paper, a new kinetic model considering both oxidation and volatilization kinetics is established and applied to analyze the oxidation of SiC-B₄C-xAl₂O₃ ceramics and other systems in various oxidation conditions. The effects of diffusion area and volume changes during the oxidation process are considered in this model. The physical meaning of each parameter in this model is explicit and simple. According to this model, the diffusion coefficient of species and the corresponding diffusion activation energy are easily available. The practicability of this model is well verified by the experimental data of SiC-B₄C-xAl₂O₃ and other systems oxidized under different conditions. In addition, the practice shows that the model is applicable not only to the systems where oxidation and volatilization coexist, but also to the system where only oxidation plays a major role. We hope the model proposed in this work can be used in other materials with more complex environments.     

Reversible formation-melting of nano-crystals in supercooled oxyfluoride germanate liquids

The nanocrystals play a critical role in generating and affecting functionalities of glass materials. Therefore, scientists have made considerable efforts in clarifying microscopic mechanisms of nanocrystal formation in glass to obtain the desired type of nanocrystals. However, the phase transitions of nanocrystals during heating have not been well understood. Here we report on a discovery of the reversible melting-formation of nanocrystals in an oxyfluoride germanate glass during heating-cooling circles. Using a differential scanning calorimetry (DSC), we detected a striking endothermic event at 925 K during heating, after the glass underwent a DSC upscan to a temperature between 925–986 K and subsequent cooling. Based on Raman spectroscopy, X-ray diffraction and transmission electron microscopy, the endotherm is attributed to the melting of nano-crystal BaGeF₆ (˜20 nm). An exothermal response was observed at 890 K during the DSC downscan, implying the re-formation of BaGeF₆ nano-crystals. This suggests that the melting-formation of BaGeF₆ nano-crystals is a typical first-order transition.     

Surfactant-free electrochemical synthesis of fluoridated hydroxyapatite nanorods for biomedical applications

Fluoridated hydroxyapatite (FHA) [Ca₁₀(PO₄)₆F_x(OH)_2−x, x = 0–2] is believed to be a promising calcium phosphate (CaP) to replace pure hydroxyapatite (HA) for next-generation implants, owing to its better biocompatibility, higher antibacterial activity, and lower solubility. Notably, the shape and size of the CaP crystals play key roles in their performance and can influence their applications. One-dimensional (1D) FHA nanorods are important CaP materials which have been widely used in regenerative medicine applications such as restorative dentistry. Unfortunately, the traditional synthesis methods for FHA nanorods either employ surfactants or take a relatively long time. In this study, we aimed to propose a facile synthesis route to fabricate FHA nanorods without any surfactants using an electrochemical deposition method for the first time. This study focused on preparing FHA nanorods without the assistance of any surfactant, unlike the traditional synthesis methods, to avoid chemical impurities. FHA nanorods with lengths of 124–2606 nm, diameters of 28–211 nm, and aspect ratios of 4.4–21.8 were synthesized using the electrochemical method, followed by a heat treatment. For the as-synthesized FHA nanorods, the Ca/P ratio was 1.60 and the atomic concentration of F was 2.06 at.%. An ultrastructure examination revealed that each FHA nanorod possessed long-range order, good crystallinity, and a defect-free lattice with a certain crystallographic plane orientation along the whole rod. In short, we propose a novel, surfactant-free, cost-saving, and more efficient route to synthesize FHA nanorods which can be widely applied in multiple biomedical applications, including drug delivery, bone repair, and restorative dentistry.     

A critical review of diamond like carbon coating for wear resistance applications

In recent years innovation in carbon based materials have encouraged both researchers as well as industrialists to develop materials/composites with improved tribological properties. Researchers have been fascinated to develop diamond like carbon (DLC) or carbon nanotubes (CNTs) reinforced coatings to their good corrosion resistance, excellent wear resistance, good adhesion strength, and self -lubricious nature. The present review article is mainly focused on various techniques employed in order to process DLC/CNTs coatings as well as provide a summary of DLC/CNTs deposition on different substrates. The present study includes major types, properties and tribological behavior of carbon based materials and mechanisms involved in coating deposition. The study also discusses that deposition of DLC/CNTs coatings on the substrate materials enhances the wear, corrosion and mechanical properties of the substrate.     

加权信息熵与增强局部二值模式结合的人脸识别

针对人脸识别因光照、姿态、表情、遮挡及噪声等多种因素的影响而导致的识别率不高的问题，提出一种加权信息熵（IEw）与自适应阈值环形局部二值模式（ATRLBP）算子相结合的人脸识别方法（IE （w） ATR-LBP）。首先，从原始人脸图像分块提取信息熵，得到每个子块的IEw；然后，利用ATRLBP算子分别对每个人脸子块提取特征从而得到概率直方图；最后，将各个块的IEw与概率直方图相乘，再串联成为原始人脸图像最后的特征直方图，并利用支持向量机（SVM）对人脸进行识别。在AR人脸库的表情、光照、遮挡A和遮挡B四个数据集上，IE （w） ATR-LBP方法分别取得了98.37%、94.17%、98.20%和99.34%的识别率。在ORL人脸库上，IE （w） ATR-LBP方法的最大识别率为99.85%；而且在ORL人脸库5次不同训练样本的实验中，与无噪声时相比，加入高斯和椒盐噪声后的平均识别率分别下降了14.04和2.95个百分点。实验结果表明，IE （w） ATR-LBP方法能够有效提高人脸在受光照、姿态、遮挡等影响时的识别率，尤其是存在表情变化及脉冲类噪声干扰时的识别率。     

One-step fabrication of highly self-hydroxylated TiO2 mesocrystals and photocatalytic behavior towards water splitting

TiO₂ mesocrystals have been considered as an efficient photocatalyst due to the effective charge transport. Introducing hydroxyls in TiO₂ is respected to reduce the energy barrier of hydrogen formation. Herein, a simple one-step fabrication of highly self-hydroxylated TiO₂ mesocrystals (MCs) for enhancing photocatalytic hydrogen evolution is proposed. TiO₂ single crystals (SCs), polycrystals (PCs) and MCs are obtained via regulating the pH of the precursor during hydrothermal treatment. Results indicate that the moderate alkaline condition is favorable for the synthesis of highly self-hydroxylated TiO₂ MCs. Compared with SCs, PCs and commercial P25 TiO₂ nanoparticles, MCs exhibit the best photocatalytic activity in H₂ evolution. Specifically, the maximum hydrogen evolution rate under solar light illumination (22.8 mmol/h/g) is 10.5 times higher than that of P25. Moreover, the MCs exhibit excellent catalytic stability and the hydrogen evolution rate can be maintained at 20.8 mmol/h/g under solar illumination after five cycles of reactions. The highly self-hydroxylated TiO₂ MCs are constructed from crystallographically oriented nanocrystals with abundant hydroxyls. The unique superstructure and large surface area of MCs enable the effective charge separation and transport. Moreover, the high density of hydroxyls can reduce the recombination rate of photo-generated free charges and energy barrier for hydrogen formation while facilitate light absorption. The synthesis of highly self-hydroxylated TiO₂ MCs and the underlying mechanism offer interesting insights for modifying the structure and properties of TiO₂ towards high-performance hydrogen evolution.     

Turbulent flame structure characteristics of hydrogen enriched natural gas with CO2 dilution

This paper investigated the hydrogen enriched methane/air flames diluted with CO₂. The turbulent premixed flame was stabilized on a Bunsen type burner and the two dimensional instantaneous OH profile was measured by Planar Laser Induced Fluorescence (PLIF). The flame front structure characteristics were obtained by extracting the flame front from OH-PLIF images. And the turbulence-flame interaction was analyzed through the statistic parameters. The role of hydrogen addition as well as CO₂ dilution on the features of turbulent flame were revealed by those parameters. In this work, hydrogen fractions of 0, 0.2 and CO₂ dilution ratios of 0, 0.05 and 0.1 were studied. Results showed that hydrogen addition can enhance turbulent burning velocity ST/S_L through decreasing the scale of the finer structure of the wrinkled flame front, caused by the smaller flame instability scale. In contrast, CO₂ dilution decreased turbulent burning velocity S_T/S_L due to its inactive response to turbulence perturbation and larger flame wrinkles. For all flames, the probability density function (PDF) profile of the local curvature radius R shows a bias to positive value, resulted from the flame intrinsic instability. The PDF profile of R decreases with CO₂ dilution, while the value of local curvature radius corresponding to the peak PDF is larger. This indicates that larger wrinkles structure was generated due to CO₂ dilution, which leads to the decrease in S_T/S_L as a consequence. Hydrogen addition increases the flame volume and results in more intense combustion. CO₂ dilution has a decrease effect on flame volume for both X_H2 = 0 and X_H2 = 0.2 while the decrease is obvious at X_H2 = 0.2, Z_CO2 = 0.1. In all, hydrogen enrichment improves the combustion while CO₂ can moderate combustion. Therefore, adding hydrogen and CO₂ in natural gas can be a potential method for adjusting the combustion intensity in combustion chamber during the combustor design.     

Influence of case-carburizing and micro-defect on competing failure behaviors of Ni–Cr–W steel under gigacycle fatigue

Axial loading test was performed to investigate the influence of case-carburizing and micro-defect on competing failure behaviors of Ni–Cr–W Steel under gigacycle fatigue. The interior failures induced from inclusion and microstructural inhomogeneity become the predominant failure mode in the life regime beyond 10⁵ cycles. The case-carburizing has no effect on the fatigue strength with interior failure. Compared with the lower limit values of experimental S–N data, the predicted results by using GP distribution is relatively suitable. From the viewpoint of reliability, the modeling method of interior S–N curve with the maximum defect size at a given probability is satisfactory.     

Kissing bond detection in structural adhesive joints using nonlinear dynamic characteristics

In this paper, the effect of kissing bond on nonlinear dynamic behavior of structures with flexible adhesive joint is investigated. Bilinear characteristic due to opening and closing in kissing bond region results in nonlinear dynamic behavior of the structure such as harmonic distortion in response to harmonic excitation. So, the higher-order harmonics can be considered as Nonlinear Damage Indicator Functions (NDIF) for the purpose of damage identification. A two-dimensional (2D) finite element model of a beam connected to a rigid support via a flexible adhesive layer is used to investigate the efficiency of the proposed NDIFs in kissing bond detection. Kissing bond is introduced to the model via contact elements. NDIFs are extracted for the finite element model using single tone stepped-sine test simulation. Parameters such as amplitude of excitation, size and location of kissing bond region as well as friction between kissing surfaces, are studied. The results proved that the NDIFs are sensitive to the size and location of kissing bond. Consequently, in an experimental damage identification procedure, NDIFs can be used as an indicator of kissing bond type damages in adhesive joints.     

X-ray photoelectron spectroscopy of the MAB phases,MoAlB, M2AlB2 (M = Cr,Fe), Cr3AlB4 and their binary monoborides

Interest in the nanolaminated MAB phases, wherein M is a transition metal, A is typically Al, and B is boron, has increased in recent years because some them have attractive properties, such as the high-temperature oxidation resistance of MoAlB or the near room-temperature active magnetic refrigeration capabilities of Fe₂AlB₂ . Herein, X-ray photoelectron spectroscopy is used to measure the binding energies (BE) of core electrons in the MAB phases, MoAlB, Cr₃AlB₄ and M₂AlB₂ (M = Cr, Fe). The BEs of the ternaries were then compared to those of their structurally related binaries, MoB, CrB, and FeB. In all these borides, a large, positive shift in the B 1 s BE relative to that of elemental B was observed. In contrast, the BE shifts of the M and Al atoms were found to be within 0.5 eV of the corresponding pure elements. These results indicate the strong role of covalent and metallic bonding in the MAB phases.