Effect of microstructure and mechanical properties on cutting force of different cast irons with similar tensile strength

Flake graphite iron, compacted graphite iron and spheroidal graphite iron with various tensile strengths were cast. They were selected and grouped according to roughly the same tensile strength, and then the main cutting force in each group was measured and compared. The microstructures of different cast irons were characterized. The relationship between the cutting force and microstructure was established. Results show that the graphite morphology in cast irons determines the strength. In order to obtain the same strength of the cast iron with sharply edged graphite, more or finer pearlite in the matrix is needed. Graphitic cast irons with high pearlite content and smaller pearlite interlamellar spacing have higher hardness. For the cast irons with different graphite morphologies, but almost the same tensile strength, the main cutting force is obviously different, along with the hardness. Harder cast irons have a greater cutting force, but the difference in cutting force is not proportional to hardness.

Role of trivalent antimony in the removal of As, Sb, and Bi impurities from copper electrolytes

The role of trivalent antimony was investigated in removing As, Sb, and Bi impurities from a copper electrolyte. Puri- fication experiments were carried out by adding a various concentrations of Sb（III） ions in a synthetic electrolyte containing 185 g/L sulfuric acid, 45 g/L Cu2＋, 10 g/L As, and 0.5 g/L Bi under stirring at 65℃ for 2 h. The electrolyte was filtered, and the structure, morphology and composition of the precipitate were analyzed by means of chemical analysis, scanning electron mi- croscopy （SEM）, X-ray diffraction （XRD）, transmission electron microscopy （TEM）, and IR spectroscopy. The precipitate is composed of irregular lumps which are agglomerated by fine dendritic and floccus particles, and it mainly consists of As, Sb, Bi, and O elements. Characteristic bands in the IR spectra of the precipitate are As-OX （X=As, Sb, Bi）, Sb-OY （Y=Sb, Bi）, O-As-O1 As-OH, Sb-OH, and O-H. The precipitate is a mixture of microcrystalline SbAsQ, （Sb,As）203, and amorphous phases. As, Sb, and Bi impurities are effectively removed from the copper electrolyte by Sb（III） ions attributing to these pre- cipitates.

Additive effects on tin electrodepositing in acid sulfate electrolytes

The effects of additives on the stannous reduction of an acid sulfate bath were investigated using cyclic and linear sweep voltammetry, electrochemical impedance spectroscopy （EIS）, and microstructure analysis. In the absence of additives, tin coatings are rough, and the tin electrodepositing is a single-step reduction process accompanied by hydrogen gas evolution. The addition of tartaric acid produces a slight reduction in the peak current of stannous reduction and has an appreciably positive effect on the stability of the acidic tin bath. Both benzylidene acetone and polyoxyethylene octylphenol ether hinder the stannous reduction and greatly suppress the hydrogen gas evolution. Formaldehyde slightly decreases the peak current density of stannous reduction and serves as an auxiliary brightener in the acid sulfate bath. The presence of mixed additives greatly suppresses the stannous reduction and hydrogen gas evolution and consequently produces a significantly smoother and denser tin coating. The （112） crystal face is found to be the dominant and preferred orientation of tin deposits.

Urea-induced interfacial engineering enabling highly reversible aqueous zinc-ion battery

Aqueous zinc-ion batteries(AZIBs)have been regarded as prospective rechargeable energy storage devices because of the high theoretical capacity and low redox potential of Zn metal.However,the uncontrollable formation of dendrites and the water-induced side reactions at the Zn/electrolyte interface,and the poor reversibility under a high current density(>2 mA·cm^(-2))and large area capacity(>2 mAh·cm^(-2))still limit the practical applications of AZIBs.Therefore,a strategy that can overcome these difficulties is urgently needed.Here,we introduce an environmentally friendly and low-cost additive,namely urea,to the electrolyte of AZIBs to induce uniform Zn deposition and suppress the side reactions.Measurements of the adsorption behavior,electrochemical characterization,and observations of the morphology revealed the interfacial modification induced by urea on the Zn/electrolyte interface,demonstrating its huge potential in AZIBs.Consequently,the long-term cycling stability(over2100 h)of a Zn/Zn symmetric cell under a high current density of 5 mA·cm^(-2)and a capacity of 5 mAh·cm^(-2)was achieved with a 1 mol·L^(-1)ZnSO_(4)electrolyte with the urea additive.Additionally,the assembled Zn/NH_4V_4O_(10)full cell with urea exhibited excellent cycling performance and an outstanding average Coulombic efficiency of 99.98%.These results indicate that this is a low-cost and effective additive strategy for realizing highly reversible AZIBs.

Effect of annealing time on microstructure and mechanical properties of cryorolled AISI 310S stainless steel

AISI 310S stable austenitic stainless steel was subjected to 90%cryorolling and then annealed at 800 ℃ for 2-60 min.The effect of annealing time on the microstructure and mechanical properties was studied by optical microscopy,scanning electron microscopy,transmission electron microscopy,microhardness and tensile test.The results show that the grain size of AISI 310S stainless steel is refined to the nanometer level after 90%cryorolling,and the grain size is approximately 20 nm.With the increase in annealing time,the degree of grain recrystallization occurs more fully and completely,as the grain begins to grow and then tends to stabilize.The strength and hardness of the annealed specimens decrease with increasing annealing time,while elongation tends to increase.When the annealing time is 10 min,the yield strength increases by about 2 times compared to that of the original austenite(unrolled),and the elongation is also above 20%,which is the best preparation process for ultra-fine grain austenitic stainless steel under this experimental condition.As the annealing time treatment increases,the fracture morphology changes from mixed quasi-cleavage and ductile fracture(after cryorolling)to ductile fracture(after annealing).

Enhanced magnetic properties of SmCo/FeCo nanocomposite magnets by doping eutectic Sm-Ni alloy

In this work,we prepared SmCo/FeCo nanocomposite magnets with an enhanced magnetic performance by doping eutectic Sm-Ni alloy.The magnets without Sm-Ni alloy,with a grain size of 5-12 nm and an average size of~ 9 nm,are composed of Sm_(2)Co_(17) phase and FeCo phase,leading to a relatively low remanence of 0.0365A·m^(2)·g^(-1) and coercivity of 0.15 T,respectively.After doping 2.5 wt% Sm-Ni alloy,there is no obvious change on the grain size of SmCo/FeCo magnets.

Recent advances and perspective in metal coordination materialsbased electrode materials for potassium-ion batteries

Recently,to ameliorate the forthcoming energy crisis,sustainable energy conversion and storage devices have been extensively investigated.Potassium-ion batteries(KIBs)have aroused widespread attention in these very active research applications due to their earth abundance and similar low redox potential compared to Li-ion batteries(LIBs).It is critical to develop electrode materials with large ion diffusion channels and robust structures for long cycling performance in KIBs.Metal coordination materials,including metal-organic frameworks,Prussian blue,and Prussian blue analogue,as well as their composites and derivatives,are known as promising materials for high-performance KIBs due to their open frameworks,large interstitial voids,functionality and tailorability.In this review,we give an overview of the recent advances on the application of metal coordination materials in KIBs.In addition,the methods to enhance their K-ion storage properties are summarized and discussed,such as morphology engineering,doping,as well as compositing with other materials.Ultimately,some prospects for future research of metal coordination materials for KIBs are also proposed.

Microstructure Evolution and Microhardness of Ultrafine-grained High Carbon Steel during Multiple Laser Shock Processing

Surface microstructure and microhardness of （ferrite＋ cementite） microduplex structure of the ultrafine- grained high carbon steel after laser shock processing （LSP） with different impact times were investigated by means of scanning electron microscopy （SEM）, transmission electron microscopy （TEM）, X-ray diffraction （XRD） and microhardness measurements. Equiaxed ferrite grains were refined from 400 to 150 nm, and the cementite lamellae were fully spheroidized, with a decrease of the particle diameter from 150 to 100 nm as the impact times increased. The cementite dissolution was enhanced significantly. Correspondingly, the lattice parameter of α-Fe and microhard- hess increased with the impact times.

Impacts of multiple laser shock processing on microstructure and mechanical property of high-carbon steel

Multiple laser shock processing （LSP） impacts on microstructures and mechanical properties were investigated through morphological determinations and hardness testing. Microscopic results show that without equal channel angular pressing （ECAP）, the LSP-treated lamellar pearlite was transferred to irregular ferrite matrix and incompletely broken cementite particles. With ECAP, LSP leads to refinements of the equiaxed ferrite grain in ultrafine-grained microduplex structure from 400 to 150 nm, and the completely spheroidized cementite particles from 150 to 100 nm. Consequentially, enhancements of mechanical properties were found in strength, microhardness and elongations of samples consisting of lamellar pearlite and ultrafine-grained microduplex structure. After LSP, a mixture of quasi-cleavage and ductile fracture was formed, different from the typical quasi-cleavage fracture from the original lamellar pearlite and the ductile fracture of the microduplex structure.

Recent progress of two-dimensional metal-base catalysts in urea oxidation reaction

Urea oxidation reaction(UOR)is an auxiliary water electrolysis hydrogen production technology developed in recent years to replace oxygen evolution reaction and reduce energy consumption,which can produce hydrogen more efficiently by low theoretical potential,reduce the average cost of electrochemical hydrogen production,and is a frontier research hotspot for renewable hydrogen energy.Two-dimensional(2D)nanomaterials as electrocatalysts have many favorable potential,such as it can effectively reduce the resistivity of materials and increase the specific surface area with certainty.This paper reviews the application of 2D materials in UOR in alkaline electrolytes.And a cross-sectional comparison of various material performance data including overpotential,Tafel slope,electrochemical active surface area(ECSA)and it stability test was conducted,which could illustrate the differences between materials composed of different elements.In addition,the main challenges hindering the progress of research on 2D materials in urea electrocatalysis processes and promising materials in this field in future are summarized and prospected.It is believed that this review will contribute to designing and analyzing highperformance 2D urea electrocatalysts for water splitting.