Effect of low concentration electrolytes on the formation and corrosion resistance of PEO coatings on AM50 magnesium alloy

In this paper,the formation process,morphology,and electrochemical performance of PEO coatings on AM50 magnesium alloy prepared in low concentration phosphate,aluminate,and phosphate-aluminate electrolytes were systematically studied.The results show that the coatings prepared from the phosphate electrolytes have a higher thickness and better corrosion resistance properties compared to the other electrolytes.The coatings prepared from low concentration phosphate-aluminate mixed electrolytes have slightly thinner thickness,a similar coating structure and an order of magnitude lower value of electrochemical impedance compared with phosphate electrolyte coatings.The Coatings prepared from low concentration aluminate electrolytes have the lowest thickness and the worst corrosion resistance properties which gets close to corrosion behavior of the bare AM50 under the same test conditions.Considering application,coatings prepared from single low concentration phosphate electrolytes and low concentration phosphate-aluminate electrolytes have greater potential than single low concentration aluminate coatings.However,reducing the electrolyte concentrations of coating forming ions too much has negative influence on the coating growth rate.

Sc元素添加对双辊铸轧Al−Cu−Li−Mg−Zr基合金热处理的影响

提出制备含Sc的Al−Cu−Li−Mg−Zr基合金带材的工艺方案。即先采用双辊铸轧技术制备近净形状的3 mm厚带材,再对其进行均匀化/固溶处理。研究两种Al−Cu−Li−Mg−Zr基双辊铸轧合金,其中一种添加质量分数为0.17%的Sc,另一种未添加Sc。两种合金均先在300℃下退火30 min,然后在450℃下退火30 min以及530℃下退火30 min,随后进行室温水淬。前两段退火后组织中生成了细小、弥散的Al_(3)Zr/Al_(3)(Sc,Zr)颗粒。最后的退火步骤起到了均匀化/固溶处理的作用。双辊铸轧材料的细小晶粒结构使含有主要合金元素的原始颗粒在较短的退火时间内溶解。缩短保温时间可以限制表面层中Li的耗尽和Al_(3)Zr/Al_(3)(Sc,Zr)弥散相的明显粗化。铸态含Sc材料已经具有明显细小的晶粒结构,而经均匀化/固溶处理后生成的Al_(3)(Sc,Zr)弥散相抑制了晶粒在高温下发生粗化。在后续180℃下时效处理后,形成了θʹ(Al_(2)Cu)、T1(Al_(2)CuLi)和S'(Al_(2)CuMg)强化相。在峰值时效状态下,屈服强度提高了200 MPa,这一数值与类似直接冷却铸造材料的相当,从而证实了所提方案的合理性。

A combined computational/experimental study of anode-concerned voltage drop in aqueous primary Mg-air batteries

The voltage drop appearing at Mg anode-electrolyte interface is a critical issue for the battery power and energy density of aqueous primary Mg-air batteries.The respective voltage loss is typically assigned to the deposits layer forming on the anode surface during discharge.In this work,we experimentally and computationally investigate the critical factors affecting the voltage drop at Mg anode towards a deeper understanding of the contribution of deposit and its growth.A two-dimensional(2D)mathematical model is proposed to compute the voltage drop of Mg-0.15Ca wt.%alloy(Mg-0.15Ca)by means of a semi-empirical formulas and experiments-based modification model,considering the effect of discharge current density,the negative difference effect(NDE)and surface deposits layer itself.This model is utilized to simulate the discharge potential of the anode at predefined experimental current densities.The computed voltage drop(half-cell voltage)is in good agreement with the experimental value.The applicability of the mathematical model is successfully validated on the second material(namely high-purity Mg).

Carbon Material with Fibonacci Parastichy Structure

The curd of Romanesco broccoli was carbonized at 900°C under argon atmosphere in a gold furnace chamber. The carbonization afforded a carbon material with a fine logarithmic spiral on the surface, resembling the Fibonacci parastichy structure of the Romanesco broccoli flower bud. The carbonized “flower bud” structure was observed under scanning electron microscopy. Infrared absorption spectra and X-ray photoelectron spectroscopy measurements confirmed the chemical structure and component of the carbon material.

Exploring the contribution of oxygen reduction reaction to Mg corrosion by modeling assisted local analysis

Oxygen reduction reaction(ORR)has been disclosed in recent studies as a significant secondary cathodic process during magnesium corrosion.This work elaborates on the contribution of ORR to the total corrosion process of pure Mg at different impurity levels in NaCl electrolyte with the assistance of local techniques.A finite element based numerical model taking into account the contribution of ORR during the corrosion of the Mg test materials has been designed in this study considering the local oxygen concentration.Respective computational simulations were calibrated based on the experimental data and evaluated accordingly.Finally,the simultaneous monitoring of local concentration of H_(2) and O_(2),and the combined modeling study reveal the relation between ORR and hydrogen evolution reaction.

Micro-alloyed Mg-Ca:Corrosion susceptibility to heating history and a plain problem-solving approach

The exceptionally low corrosion rate(∼0.1 mm y^(–1)in concentrated NaCl solution for 7 days)enables lean Mg-Ca alloys great potential for diverse applications,particularly if relevant properties(e.g.mechanical strength,electrochemical performance,etc.)can be enhanced by thermomechanical processing.However,herein it is demonstrated that the corrosion performance of lean Mg-Ca is susceptible to the heating process.The corrosion rate of Mg-0.15 wt%Ca alloy is remarkably accelerated after annealing even for a short time(4 h at 400℃)because Fe precipitation readily takes place.Fortunately,it is found that micro-alloying with dedicated additional elements is able to solve this problem.Nevertheless,the problem-solving capability is dependent on the element category,particularly the ability of the alloying element to constrain the Fe precipitation.Among the three studied elements(i.e.Sn,Ge and In),only In shows good competence of restricting the formation of Fe-containing precipitates,thereby contributing to retention of the superior corrosion resistance after annealing even at a rigorous condition(24 h at 450℃).The finding creates good foundation for follow-up work of developing lean Mg-Ca-based alloys combining high corrosion resistance,superior electrochemical performance with excellent mechanical properties for applications as biodegradable implants and anode materials for aqueous batteries.

In-situ LDHs growth on PEO coatings on AZ31 magnesium alloy for active protection:Roles of PEO composition and conversion solution

In this work,plasma electrolytic oxidation(PEO)coatings were produced on magnesium alloy AZ31 in aluminate,silicate and phosphate-based electrolytes,and followed by hydrothermal treatments in order to synthesis layered double hydroxides(LDHs)based nanocontainers.LDHs synthesis was done in three different growth solutions(deionized water,sodium nitrate and aluminum nitrate containing solution).In frame of this work it was shown,that it was difficult to form LDHs on Si-based PEO coating,due to more stable silicate phases in comparison with aluminate and phosphate phases in respective PEO coatings.The obtained hybrid LDH/PEO coatings were characterized using SEM,EDS and GDOES,and then the corrosion protection was further investigated by EIS.Based on the obtained results,it was confirmed that,the hydrothermal treatments in Al^(3+)containing solution played an important role on overall corrosion resistance for phosphate and silicate-based PEO coatings,but not for Al-based PEO coatings.

Generalized uncertainty principle from long-range kernel effects:The case of the Hawking black hole temperature

We prove the existence of an analogy between spatial long-range interactions,which are of the convolution-type introduced in non-relativistic quantum mechanics,and the generalized uncertainty principle predicted from quantum gravity theories.As an illustration,black hole temperature effects are discussed.It is observed that for specific choices of the moment's kernels,cold black holes may emerge in the theory.

Evaluation of Reactive Oxygen Species (ROS) Generated on the Surface of Copper Using Chemiluminesence

The antibacterial activity of copper is well-known from an ancient civilization, however, its biocidal mechanism has not been necessarily elucidated. Notwithstanding up to now, mainly 4 processes have been proposed. Among them, it is cleared that 4 kinds of reactive oxygen species (ROS): hydroxyl radical ·OH, hydrogen per oxide H2O2, superoxide anion ·O-2 and singlet oxygen 1O2, play an important role for contact-killing of bacteria, viruses and fungi. In this paper, generation of ROS on the surfaces of copper plates heated from room temperature to 673 K for 4.2 × 102 s in air, was investigated using the chemiluminescence. ROS have been evaluated by selecting the most suitable scavengers, such as 2-propanol for ·OH, sodium pyruvate for H2O2, nitro blue tetrazolium for ·O-2, and sodium azide NaN3 for 1O2. At the same time the outermost surface of copper, on which thin film of cuprous oxide Cu2O was first formed and then cupric oxide CuO was laminated on Cu2O, was examined by thin-film XRD and TEM analysis to estimate the amounts and kinds of copper oxides. It was found that the most amounts of ROS were obtained for the 573 K-heated Cu plate and they were composed of ·OH, H2O2, and ·O-2..

细晶Al-5356合金在低应变速率下基于高分辨率应变测量的“异常瞬时蠕变”(英文)

极低应变速率下(<10-10s-1)的瞬时蠕变仍然未知。由于应变分辨率低(～10-6),传统的单轴拉伸/压缩等蠕变测试技术并不能满足此蠕变区的测试要求。采用具有高应变分辨率的螺旋弹簧蠕变试验法,研究Al-5356合金在温度范围为0.4Tm^0.8Tm(Tm为熔点的绝对温度)、应变速率小于10-10s-1的瞬时蠕变行为。采用透射电子显微镜研究蠕变微观组织以揭示极低应变速率下的瞬时蠕变机制。实验结果首次显示了一些异常蠕变行为:"高温强化"(T>Tp,Tp为发生相变的温度,Tp=0.58Tm)或"中温弱化"(0.4Tm<T≤Tp)和"双正常型蠕变"(蠕变曲线包含两次加工硬化阶段(T=Tp))。试样经中温(0.58Tm)蠕变后(1×10-4),微观组织中发现有大量等间隔割阶的塞积位错和从晶界发射的弧形位错。当温度高于523K时,β-Al3Mg2相溶解引起固溶Mg量增加,因此,异常蠕变行为可能归因于蠕变过程中相转变引起的固溶强化的差异。

纯铜在低温和极低应变速率下的初始蠕变和粘弹性回复（英文）

采用高应变分辨率的螺旋弹簧蠕变试验法,研究晶粒尺寸d_g为40μm纯铜在低温(T<T_m,T_m为纯铜的熔点)和应变速率小于1×10^(-10) s^(-1)条件下的蠕变和粘弹性回复行为。采用基于蠕变曲线尺度因子的数据解析法,代替传统基于外推的稳态蠕变速率的蠕变数据解析法。结果表明:纯铜低温、低应力初始蠕变行为可由幂律蠕变方程描述,因为幂律蠕变方程初始参数不随蠕变时间改变而变化;粘弹性应变为弹性应变的1/6;粘弹性应变速率的对数和粘弹性应变的对数呈线性关系(斜率为1)。因此,纯铜低温、低应力蠕变可能由三维位错网的收缩机制控制。

Corrosion and wettability of PEO coatings on magnesium by addition of potassium stearate

Hydrophobic PEO coatings were fabricated in an electrolyte containing potassium stearate.The wetting behaviour of coated samples was studied using dynamic and static contact angle.Also,the corrosion behaviour of the samples was evaluated by polarization method.The dynamic contact angle and hysteresis of the contact angle for PEO coating were evaluated by Wilhelmy plate method.There was an increase in the contact angle of the nanocomposite and traditional PEO coatings when potassium stearate was added to the electrolyte up to 130°.The more hydrophobic coatings,showed more corrosion resistance in 3.5 wt.%NaCl solution.The synergistic effect of potassium stearate and nanoparticles increased the hydrophobicity because of assembling of fatty acid on ceramic powder.

Cu-Zn-Al2O3 nanocomposites: study of microstructure, corrosion, and wear properties

Alumina nanoparticles were added to a Cu-Zn alloy to investigate their effect on the microstructural,tribological,and corrosion properties of the prepared alloys. Alloying was performed using a mixture of copper and zinc powders with 0vol% and 5vol% of α-Al nanopowder in a satellite ball mill. The results showed that the Cu-Zn solid solution formed after 18 h of mechanical alloying. The mechanically alloyed powder was compacted followed by sintering of the obtained green compacts at 750°C for 30 min. Alumina nanoparticles were uniformly distributed in the matrix of the Cu-Zn alloy. The tribological properties were evaluated by pin-on-disk wear tests,which revealed that,upon the addition of alumina nanoparticles,the coefficient of friction and the wear rate were reduced to 20% and 40%,respectively. The corrosion properties of the samples exposed to a 3.5wt% Na Cl solution were studied using the immersion and potentiodynamic polarization methods,which revealed that the addition of alumina nanoparticles reduced the corrosion current of the nanocomposite by 90%.

Clarifying the influence of albumin on the initial stages of magnesium corrosion in Hank's balanced salt solution

The corrosion behavior of Mg,a promising biodegradable metallic material,in protein-containing pseudophysiological environment is still not fully understood.In this work,the influence of albumin on the corrosion behavior of commercially pure magnesium(CP Mg)is investigated during short-term tests in Hank’s Balanced Salt Solution(HBSS).This work focuses on the reactions at the Mg/medium interface from the perspective of the interactions among albumin,media components and substrate.Hydrogen evolution tests demonstrate that the physiological amount of albumin(40 g L^(-1))accelerates Mg corrosion in HBSS during the first few hours but slows down the degradation afterwards.The presence of albumin decreases the concentration of free Ca^(2+)in HBSS and delays formation of protective co-precipitation products on Mg surface.The evolution of local pH(differs from typically monitored bulk pH)near Mg/medium interface in albumincontaining HBSS is reported for the first time.Comparison of local and bulk pH values elucidates the pH buffering effect of albumin during the immersion period.Based on these results,adsorption,chelating and pH buffering effects are summarized as three important aspects of albumin influence on Mg corrosion.Additionally,constant replenishment of medium components is shown to be an influential factor during the Mg corrosion tests.

Evaluation of the Electroslag Remelting Process in Medical Grade of 316LC Stainless Steel

This study is focused on the effects of electroslag remelting by prefused slag （CaO, Al2O3, and CaF2） on macrostructure and reduction of inclusions in the medical grade of 316LC （316LVM） stainless steel. Analysis of the obtained results indicated that for production of a uniform ingot structure during electroslag remelting, shape and depth of the molten pool should be carefully controlled. High melting rates led to deeper pool depth and interior radial solidification characteristics, while decrease in the melting rates caused more reduction of nonmetallic inclusions. Large shrinkage cavities formed during the conventional casting process in the primary ingots were found to be the cause of the fluctuation in the melting rate, pool depth and extension of equiaxed crystals zone.

Effects of Potassium and Manganese Promoters on Nitrogen-Doped Carbon Nanotube-Supported Iron Catalysts for CO_2 Hydrogenation

氮掺杂碳纳米管(NCNTs)作为载体负载铁(Fe)纳米颗粒,可应用于CO_2多相催化加氢反应(633 K和25 bar)。当将钾(K)和锰(Mn)作为助催化剂时,Fe/NCNT展现出优异的CO_2加氢性能,在体积空速(GHSV)为3.1 L·g^(–1)·h^(–1)时转化率可达34.9%。当使用K作为助催化剂时,反应对烯烃和短链烷烃具有高的选择性。当K和Mn同时作为助催化剂时,其催化活性能够稳定地维持60 h。助催化剂Mn的结构效应通过X射线衍射、氢气程序升温还原以及近边X射线吸收精细结构进行表征。助催化剂Mn不仅能够稳定中间态FeO,且能降低程序升温还原的起始温度。通过探针反应NH3的催化分解来表征助催化剂效应。当K和Mn作为助催化剂时,Fe/NCNT具有最好的催化活性。在还原条件下,当K作为助催化剂时,Fe/NCNT具有最优异的热稳定性。

铸态Al-7Si-0.3Mg合金的连续冷却析出图(英文)

采用冷却速率为0．01～3K／s的差示扫描量热法（DSC）和冷却速率更高的淬火膨胀法研究铸态Al-7Si-0．3Mg合金淬火的析出行为。在合金冷却的过程中发生了两种析出反应，高温反应开始于淬火起始温度540℃，低温反应始于400℃左右。3K／s的淬火冷却速率已经显著抑制淬火过程中相的析出。合金T6态的硬度随着淬火速率的增快而增加，这是由合金过饱和固溶度增加而导致的。通过膨胀实验和硬度实验的结果可以估计临界冷却速率大约为60K／s。通过光学显微镜观察淬火态的铸态Al-7Si-0．3Mg合金的显微组织。结果表明：根据淬火冷却速率的不同合金的显微组织由铝一硅共晶组织、铝固溶体枝晶及枝晶间的析出相组成。

Dynamic ModeⅡfracture behavior of rocks under hydrostatic pressure using the short core in compression(SCC)method

The shear failure of rocks under both a static triaxial stress and a dynamic disturbance is common in deep underground engineering and it is therefore essential for the design of underground engineering to quantitively estimate the dynamic ModeⅡfracture toughness KⅡCof rocks under a triaxial stress state.However,the method for determining the dynamic KⅡCof rocks under a triaxial stress has not been developed yet.With an optimal sample preparation,the short core in compression(SCC)method was designed and verified in this study to measure the dynamic KⅡCof Fangshan marble(FM)subjected to different hydrostatic pressures through a triaxial dynamic testing system.The formula for calculating the dynamic KⅡCof the rock SCC specimen under hydrostatic pressures was obtained by using the finite element method in combination with secondary cracks.The experimental results indicate that the failure mode of the rock SCC specimen under a hydrostatic pressure is the shear fracture and the KⅡCof FM increases as the loading rate.In addition,at a given loading rate the dynamic rock KⅡCis barely affected by hydrostatic pressures.Another important observation is that the dynamic fracture energy of FM enhances with loading rates and hydrostatic pressures.

Microwave-assisted synthesis of CePO_4 nanorod phosphor with violet emission

Monochnic and hexagonal CePO4 nanoparticles and nanorods were successfully synthesized from Ce（NO3）36H2O and Na3PO4 121-120 solu- tions at pH 1-5 by a 180 W microwave radiation for 60 min. The products were characterized by X-ray diffraction （XRD）, Fourier transform infrared （FFIR） spectroscopy, and scanning electron microscopy （SEM）. XRD patterns revealed that the products are hexagonal CePO4 structures at pH 2-5, and monoclinic CePO4 structtLres at pH 1. SEM characterization shows that these products were nanoparticles, short nanorods, and long nanorods, controlled by the pH of the precursor solutions. Optical properties of the nanorods were also investigated by ultraviolet-visible （UV-vis） and photoluminescence （PL） spectroscopy.