High chemical stability anion exchange membrane based on poly(aryl piperidinium): Effect of monomer configuration on membrane properties

In recent years, ether-free polyaryl polymers prepared by superacid-catalyzed Friedel-Crafts polymerization have attracted great research interest in the development of anion exchange membranes(AEMs) due to their high alkali resistance and simple synthesis methods. However, the selection of monomers for high-performance polymer backbone and the relationship between polymer structure construction and properties need further investigated. Herein, a series of free-ether poly(aryl piperidinium) (PAP) with different polymer backbone steric construction were synthesized as stable anion exchange membranes. Meta-terphenyl, p-terphenyl and diphenyl-terphenyl copolymer were chosen as monomers to regulate the spatial arrangement of the polymer backbone, which tethered with stable piperidinium cation to improve the chemical stability. In addition, a multi-cation crosslinking strategy has been applied to improve ion conductivity and mechanical stability of AEMs, and further compared with the performance of uncrosslinked AEMs. The properties of the resulting AEMs were investigated and correlated with their polymer structure. In particular, m-terphenyl based AEMs exhibited better dimensional stability and the highest hydroxide conductivity of 144.2 mS/cm at 80 °C than other membranes, which can be attributed to their advantages of polymer backbone arrangement. Furthermore, the hydroxide conductivity of the prepared AEMs remains 80%–90% after treated by 2 M NaOH for 1600 h, exhibiting excellent alkaline stability. The single cell test of m-PTP-20Q4 exhibits a maximum power density of 239 mW/cm² at 80 °C. Hence, the results may guide the selection of polymer monomers to improve performance and alkaline durability for anion exchange membranes.     

A novel ultra-high-temperature oxidation protective MoSi2-TaSi2 ceramic coating for tantalum substrate

To protect refractory metal against oxidation at ultra-high temperatures, a MoSi₂-TaSi₂ ceramic coating was prepared on a pure tantalum (Ta) substrate using a novel three-step process, which included dip-coating with a molybdenum slurry, vacuum sintering, and halide-activated pack cementation (HAPC). The original coating had a MoSi₂-TaSi₂ double-layer structure from the surface to the substrate. After oxidation at 1700°C for 8 h in air, the coating exhibited a complex multi-layer structure composed of SiO₂-Mo₅Si₃-MoSi₂-(Mo,Ta)₅Si₃-TaSi₂-Ta₅Si₃ from the outer layer to the inner layer, due to the high-temperature phase transition and diffusion of Si and O. The coating effectively protected the Ta substrate at 1700°C for 12 h without failure, thereby demonstrating great improvement to its service life in an ultra-high-temperature aerobic environment. The protective effect was attributed to the integrity of the ceramic coating and the formation of a dense, uniform SiO₂ film that effectively lowered the inward oxygen diffusion rate.     

The formation of fibrous structure of polyamide 6 induced by the three-step forming process and its prominent reinforcement in nitrile rubber

Nitrile rubber (NBR) blends with excellent performance have always been a hot research topic in petroleum field. Due to the excellent performance and compatibility of polyamide 6 (PA6), it provides an opportunity for the preparation of high-performance NBR/PA6 blends. In this article, NBR/PA6 blends were prepared by the three-step molding process. Experimentally, it was found that PA6 has a prominent reinforcement effect in NBR matrix. The variation of this mechanical property was investigated from different aspects of the crystal structure, crystallinities, phase morphology, and so on. It can be cleared that the formation of fibrous structure of PA6 phase is the main factor for reinforcement of the polymer blends. Meanwhile, the formation mechanism of the special phase structure induced by the three-step process is deeply expounded and its structural evolution schematic is established. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47472.     

LaFeO3 porous hollow micro-spindles for NO2 sensing

LaFeO₃ micro-spindles with intriguing structural characteristics were synthesized using cyano-bridged coordination polymers as sacrificial templates. Within a longitudinal dimension of less than 5?µm, each micro-spindle features a hollow center contained in a mesoporous shell with hexagonal cross section. Conductometric gas sensors developed from these micro-spindles demonstrate a comprehensively improved NO₂-sensing performance over other-reported LaFeO₃ devices, including lower operating temperature (155?°C), higher sensitivity (response of 81.4% under 5?ppm) and expedited response and recovery (40?s/329?s). Such performance is enabled by a semiconducting mechanism governed by the formation and catalytic dissociation of nitrite species during NO₂ adsorption on LaFeO₃, facilitated by the special hierarchical structure of the micro-spindle.     

一种吹瓶机取送瓶机械手取瓶运动的改进设计

为了研究机械手在工作中的运动状态,提高机械手的工作效率,对一种吹瓶机机械手取送瓶的运动过程进行分析,在其取瓶靠近阶段设计出一条新的运动轨迹,并用五次多项式进行拟合.采用三次样条函数对衔接点及同步阶段轨迹进行拟合,保证了机械手速度与加速度的连续.模拟分析表明,改进后的机械手绝对速度变得平顺,绝对加速度也大幅度降低.     

Recent progress of physical failure analysis of GaN HEMTs

Gallium nitride (GaN)-based high-electron mobility transistors (HEMTs) are widely used in high power and high frequency application fields,due to the outstanding physical and chemical properties of the GaN material.However,GaN HEMTs suffer from degradations and even failures during practical applications,making physical analyses of post-failure devices extremely significant for reliability improvements and further device optimizations.In this paper,common physical characterization techniques for post failure analyses are introduced,several failure mechanisms and corresponding failure phenomena are reviewed and summarized,and finally device optimization methods are discussed.     

Highly active sites of low spin FeⅡN4species:The identification and the ORR performance

Over recent years,catalytic materials of Fe-N-C species have been recognized being active for oxygen reduction reaction(ORR).However,the identification of active site remains challenging as it generally involves a pyrolysis process and mixed components being obtained.Herein Fe₃C/C and Fe₂N/C samples were synthesized by temperature programmed reduction of Fe precursors in 15%CH₄/H₂and pure NH₃,respectively.By acid leaching of Fe₂N/C sample,only single sites of FeN₄species were presented,providing an ideal model for identification of catalytic functions of the single sites of FeN₄in ORR.A correlation was conducted between the concentration of Fe^ⅡN₄in low spin state by Mossbauer spectra and the kinetic current density at 0.8 V in alkaline media,and such a structure-performance correlation assures the catalytic roles of low spin Fe^ⅡN₄ species as highly active sites for the ORR.     

结合时间戳的指纹密钥数据加解密传输方案

目的 对于生物密钥而言，生物特征数据的安全与生物密钥的管理存储都很关键。为了构造能够应用在通信数据传输场景的生物密钥，同时保证生物特征本身的模糊性与密码学的精确性处于一种相对平衡状态，提出一种基于时间戳与指纹密钥的数据加解密传输方案。方法 利用发送方指纹特征点之间的相对信息，与保密随机矩阵生成发送方指纹密钥；借助通信双方的预先设定数与时间戳，生成接收方恢复指纹密钥时所需的辅助信息；利用发送方指纹密钥加密数据，实现密文数据的传输。结果 本文方法在仿真通信双方数据加解密的实现中，测试再生指纹密钥的识别率（GAR）与误识率（FAR）。通过实验数据分析，表明了本文提出的指纹密钥生成方法的可用性，以及指纹密钥作为数字身份所具备的可认证性，其中真实发送方的再生指纹密钥识别率可高达99.8%，并且本方案还可用于即时通信、对称加密等多种场景当中。结论 本文方法利用时间戳确定了通信事件的唯一性与不可否认性，同时实现了指纹密钥恢复时的"一次一密"。此外，方案通过保密随机矩阵实现了发送方指纹密钥的可撤销，极大程度保障了指纹数据的安全性。