Effect of nitrogen on deflagration characteristics of hydrogen / methane mixture

In order to study the influence of nitrogen on the deflagration characteristics of premixed hydrogen/methane, the explosion parameters of premixed hydrogen/methane within various volume ratios and different dilution ratios were studied by using a spherical flame method at room temperature and pressure. The results are as follows: The addition of nitrogen makes the upper limit of explosion of hydrogen/methane premixed gas drop, and the lower limit rises. For explosion hazard (F-number), hydrogen/methane premixed fuel with a hydrogen addition ratio of 10% has the lowest risk, and nitrogen has a greater impact on the dangerous degree of hydrogen and methane premixed gas whose hydrogen addition ratio does not exceed 30%. In terms of flame structure, the spherical flame was affected by buoyancy instability as the percentage of nitrogen dilution increased, but the buoyancy instability gradually decreased as the percentage of hydrogen addition increased. The addition of diluent gas reduces the spreading speed of the stretching flame and reduces the stretching rate in the initial stage of flame development. The laminar flame propagation velocity calculated by the experiment in this paper is consistent with the laminar flow velocity of the hydrogen/methane premixed gas calculated by GRI Mech 3.0. Considering the explosion parameters such as flammability limit, laminar combustion rate and deflagration index, when hydrogen is added to 70%, it is the turning point of hydrogen/methane premixed fuel.     

Microstructure and some properties of powder-pack borided Ti–5Mo–5V–8Cr–3Al alloy with special attention to the microstructure at the interface TiB/substrate

The borided layer was prepared on the surface of the Ti–5Mo–5V–8Cr–3Al alloy by powder-pack boriding at 1000°C-10h. SEM, EPMA and TEM were used to investigate the effects of alloying elements (Al, V, Mo and Cr) on the growth of TiB whiskers in the borided Ti–5Mo–5V–8Cr–3Al alloy. Wear properties of borided Ti–5Mo–5V–8Cr–3Al alloy were investigated using dry reciprocating friction tests. SEM results show that the thickness of boride layer in Ti–5Mo–5V–8Cr–3Al alloy is thinner than that in the Cp-Ti. This is attributed to the enrichment of alloying elements especially V in TiB/substrate by TEM, which hinders the diffusion of B atoms, thus resulting in the short and thick TiB whiskers in Ti–5Mo–5V–8Cr–3Al alloy. Borided Ti–5Mo–5V–8Cr–3Al alloy has the better wear resistance than as-received alloy.     

Effect of SnO–P2O5–MgO glass addition on the ionic conductivity of Li1.3Al0.3Ti1.7(PO4)3 solid electrolyte

NASICON-type structured compounds Li_1+xM_xTi_2-x(PO₄)₃ (M = Al, Fe, Y, etc.) have captured much attention due to their air stability, wide electrochemical window and high lithium ion conductivity. Especially, Li_1.3Al_0.3Ti_1.7(PO₄)₃ (LATP) is a potential solid electrolyte due to its high ionic conductivity. However, its actual density usually has a certain gap with the theoretical density, leading the poor ionic conductivity of LATP. Herein, LATP solid electrolyte with series of SnO–P₂O₅–MgO (SPM, 0.4 wt%, 0.7 wt%, 1.0 wt%, 1.3 wt%) glass addition was successfully synthesized to improve the density and ionic conductivity. The SPM addition change Al/Ti–O bond and P–O bond distances, leading to gradual shrinkage of octahedral AlO₆ and tetrahedral PO₄. The bulk conductivity of the samples increases gradually with SPM glass addition from 0.4 wt% to 1.3 wt%. Both SPM and the second-phase LiTiPO₅, caused by glass addition, are conducive to the improvement of compactness. The relative density of LATP samples increases first from 0 wt% to 0.7 wt%, and then decreases from 0.7 wt% to 1.3 wt% with SPM glass addition. The grain boundary conductivity also changes accordingly. Especially, the highest ionic conductivity of 2.45 × 10^?4 S cm^?1, and a relative density of 96.72% with a low activation energy of 0.34 eV is obtained in LATP with 0.7 wt% SPM. Increasing the density of LATP solid electrolyte is crucial to improve the ionic conductivity of electrolytes and SPM glass addition can promote the development of dense oxide ceramic electrolytes.     

Hydrogen storage comparison of M doped vanadium oxide nanotubes (M = Mo,Zr and W): A molecular simulation study

Zr, Mo and W doped Vanadium oxide nanotube were considered as remarkable materials for hydrogen storage applications. Monte Carlo molecular simulation was performed to study the adsorption behavior of hydrogen molecules on Vanadium oxide nanotubes (VONTs). The effects of temperature, pressure and mole percent of hydrogen on adsorption capacity of VONTs were investigated to provide deep insight of adsorption behavior. The results represented that hydrogen adsorption is an increasing function of pressure and at about 50 MPa all three metal doped VONT has maximum hydrogen capacity. At 5 MPa and room temperature, the hydrogen capacities of Mo, W and Zr doped VONTs were 1.39, 0.88 and 1.43 w% respectively. With temperature increment up to room temperature, more reduction in initial hydrogen capacity were observed in Mo and Zr doped VONTs.Evaluating hydrogen adsorption of Zr doped VONT from pure and hydrogen /nitrogen mixtures at 300 K indicated that under 2 Mpa, modifications in adsorption capacities were insignificant after N2 addition to the environment. Therefore, Zr doped VONT in hydrogen /nitrogen mixture environment can act as a capable adsorbent for Hydrogen storage system in comparison with Mo and W doped VONTs.     

022Cr17Ni12Mo2钢制水灰流量检测器焊接修复工艺

为了准确定位并修复022Cr17Ni12Mo2钢制水灰流量检测器装置内部出现的冲蚀磨损缺陷坑，结合流量检测器装置的实际工况，提出了采用TIG焊接方法修复冲蚀磨损缺陷坑的措施。制定了经济实用的焊接方法，设置了合理的焊接工艺参数，并对该工艺参数下的焊接修复件进行了相关检测。检测结果表明，修复部位满足相关技术条件要求，质量可靠，修复后装置试运行稳定有效，完全达到了使用要求。说明制定的焊接修复工艺合理可行，可用于同类缺陷的焊接修复工作。     

Novel hydrophilic N-halamine polymer with enhanced antibacterial activity synthesized by inverse emulsion polymerization

N-halamine-based antibacterial agents have high efficiency and rechargeable antibacterial properties. However, their applications are limited due to their complex synthetic process and fuzzy antibacterial mechanism. In this study, a novel N-halamine antibacterial polymer was synthesized by inverse emulsion polymerization and characterized by Fourier transform infrared, nuclear magnetic resonance, scanning electron microscopy, thermogravimetric analysis, and X-ray photoelectron spectroscopy. Due to the difficulty of purification, most of the subjects studied previously were hydrophobic polymers, while little research on hydrophilic polymers. In this experiment, this difficulty was overcome by controlling the dosage of sodium hypochlorite and methods of dialysis. Because of the complex cell structure of Gram-negative bacteria, it is difficult for N-halamines to release the oxidizing chlorine into the cell. However, the hydrophilic N-halamines can solve this problem, which showed a stronger antibacterial effect on Gram-negative Escherichia coli synthesized in this study. In addition, the particle size and hydrophilic property of the polymer were changed by changing the amount of initiator, and the differences in their antibacterial properties were studied. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47419.     

Growth of Ni/Mo/Cu on carbon fiber paper: An efficient electrocatalyst for hydrogen evolution reaction

The exploration of efficient catalysts toward hydrogen evolution reaction (HER) is still an urgent task. In this paper, Ni/Mo/Cu/C and Ni/Mo/C electrode were obtained by conventional pulse voltammetry, which acted as cathode in microbial electrolysis cells (MECs). The prepared samples are analyzed using SEM, XRD, XPS and electrochemical analysis techniques. Results indicated that the Ni/Mo/Cu coating has a rough and globular structure and presents high current density, a lower Tafel slope of 23.9 mV/dec than 30 mV/dec of Pt, which exceeds the electrochemical activity of Pt electrode. Its remarkably enhanced electrocatalytic activity is attributed to the high surface area, high conductivity as well as synergistic interaction among Ni, Mo and Cu.     

Structural,thermal and dielectric properties of AlN–SiC composites fabricated by plasma activated sintering

Highly dense AlN–SiC composites with various SiC additions (0–50?wt-%) were fabricated at 1800°C by plasma activated sintering. The effect of SiC addition on structural, thermal and dielectric properties as well as microwave absorbing performance of the composites was investigated. The thermal conductivity decreases with increasing SiC addition, from 68.7 W (m?K)^?1 for 0?wt-% SiC to 19.38?W (m?K)^?1 for 50?wt-% SiC. On the contrary, the permittivity and dielectric loss increase gradually, from 7.6–8.5 to 22–26.7 and from 0.02–0.1 to 0.2–0.53, respectively. AlN–SiC composite with better thermal and dielectric properties in 30?wt-% SiC, whose thermal conductivity and dielectric loss are found to be 24.88?W (m?K)^?1 and 0.15–0.74, respectively. Furthermore, the composite exhibits microwave absorbing performance with the minimum reflection loss (RL) of ?16.5 dB at 15.5 GHz and the frequency range of 2.6 GHz for RL below ?10 dB (90% absorption).     

铁素体基Ti-Mo高强钢连续冷却相变及组织性能

摘要：为了深入了解铁素体基Ti-Mo高强钢在连续冷却相变过程中组织及硬度的变化及其原因，通过热膨胀法、金相及硬度等实验研究了Ti-Mo微合金钢在连续冷却条件下组织及性能的变化，探讨了冷却速率对组织、硬度及相变行为的影响机理，揭示了（Ti，Mo）C在奥氏体和铁素体中Ti/Mo原子比变化的原因。结果表明，随着冷却速率由0.06℃/s增加至17.9℃/s，组织依次为多边形铁素体+珠光体→多边形铁素体+粒状贝氏体→粒状贝氏体，硬度由144HV逐渐增大至228HV。当冷速由0.14℃/s增大至0.90℃/s时，组织中多边形铁素体比例不断增大，珠光体比例不断降低，硬度的提高主要来自于铁素体晶粒尺寸的细化及纳米级（Ti，Mo）C粒子的增多；当冷速由1.79℃/s增大至17.9℃/s时，组织中多边形铁素体比例不断降低，贝氏体比例不断提高，硬度的提高主要是由于贝氏体组织的细化及其比例的增加。（Ti，Mo）C粒子主要有2类：一类是奥氏体中析出的10～20nm的粒子，Ti原子数分数约为88%，另一类是铁素体中析出的小于10nm的粒子，Ti原子数分数约为68%，EDS测量结果与计算结果大致相当。     

基体稀释或基体匹配石墨炉原子吸收光谱法测定土壤样品中铅和镉

用石墨炉原子吸收光谱法测定土壤样品中Pb和Cd时,有时候直接按照方法标准GB/T 17141—1997操作,测定结果不能满足质控要求。研究结果表明,目标元素系列标准溶液中,分别含和不含土壤基体元素Na、Mg、Al、Si、Fe、Ca等元素混合成分时,校准曲线斜率明显不同。为减小基体效应的影响,基于文献调研和实验结果,对上述方法标准实验步骤进行了下列改进:(1)取相同体积实际样品消解液混合后,定量加入到用于建立校准曲线的系列标准溶液中,用于基体匹配;(2)对消解液进行适度稀释,仍采用标准溶液建立校准曲线。用4个土壤标样和土壤样品加标测定结果对改进后的方法进行了验证,结果表明,基体稀释法测定Pb的回收率范围分别为90.4%~114%;测定低含量Cd时,回收率范围为84.1%~125%。基体匹配法测定Pb和Cd的回收率范围分别为93.0%~105%和102%~119%,基本满足土壤样品中重金属回收率为80%~120%的质控要求。样品中痕量镉在测定下限附近时,应严格控制稀释倍数,或采用基体匹配法测定。改进后的操作步骤适合日常检测工作中大批量土壤样品中Pb和Cd的准确测定。