Design of a low-alloy high-strength and high-toughness martensitic steel

To develop a high strength low alloy (HSLA) steel with high strength and high toughness, a series of martensitic steels were studied through alloying with various elements and thermodynamic simulation. The microstructure and mechanical properties of the designed steel were investigated by optical microscopy, scanning electron microscopy, tensile testing and Charpy impact test. The results show that cementite exists between 500℃ and 700℃, M₇C₃ exits below 720℃, and they are much lower than the austenitizing temperature of the designed steel. Furthermore, the Ti(C,N) precipitate exists until 1280℃, which refines the microstructure and increases the strength and toughness. The optimal alloying components are 0.19% C, 1.19% Si, 2.83% Mn, 1.24% Ni, and 0.049% Ti; the tensile strength and the V notch impact toughness of the designed steel are more than 1500 MPa and 100 J, respectively.     

Microstructure and stress rupture properties of polycrystal and directionally solidified castings of nickel-based superalloys

A new directionally solidified Ni-based superalloy DZ24, which is a modification of K24 alloy without rare and expensive elemental additions, such as Ta and Hf, was studied in this paper. The microstructure and stress rupture properties of conventionally cast and directionally solidified superalloys were comparatively analyzed. It is indicated that the microstructure of K24 alloy is composed of γ, γ′, γ/γ′ eutectics and MC carbides. Compared with the microstructure of K24 polycrystalline alloy, γ/γ′ eutectic completely dissolves into the γ matrix, the fine and regular γ′ phase reprecipitates, and MC carbides decompose to M₆C/M₂₃C₆ carbides after heat treatment in DZ24 alloy. The rupture life of DZ24 alloy is two times longer than that of K24 alloy. The more homogeneous the size of γ′ precipitate, the longer the rupture life. The coarsening and rafting behaviors of γ′ precipitates are observed in DZ24 alloy after the stress-rupture test.     

Evolution of carbides and carbon content in matrix of an ultra-high carbon sintered steel during heat treatment process

DTA, thermal expansion, XRD, and SEM were used to evaluate the effect of quenching temperature on the mechanical properties and microstructure of a novel sintered steel Fe-6Co-1Ni-5Cr-5Mo-1C. Lattice parameters and the mass fraction of carbon dissolved in the matrix of the steel quenched were investigated. It is discovered that the hardness of the steel increases with quenching temperature in the range of 840-900℃ and remains constant in the range of 900 to 1100℃. It decreases rapidly when the temperature is higher than 1100℃. The mass fraction of carbon dissolved in the matrix of the steel quenched at 840℃ is 0.38, but when the quenching temperature is increased to 1150℃, it increases to 0.98. The carbides formed during sintering are still present at grain boundaries and in the matrix of the steel quenched at low quenching temperatures, such as 840℃. When the quenching temperature is increased to 1150℃, most of the carbides at grain boundaries are dissolved with just a small amount of spherical M₂₃C₆ existing in the matrix of the quenched steel.     

High-temperature properties and microstructure of Mo microalloyed ultra-high-strength steel

The high-temperature mechanical properties and microstructure of forging billets of C-Si-Mn-Cr and C-Si-Mn-Cr-Mo ultra-high-strength cold-rolled steels (tensile strength≥1000 MPa, elongation≥10%) were studied. Through the comparison of reduction in area and hot deformation resistance at 600–1300°C, the Mo-containing steel was found to possess a higher strength and a better plasticity than the Mo-free one. The equilibrium phase diagram and atom fraction of Mo in different phases at different temperatures were calculated by Thermo-Calc software (TCW). The results analyzed by using transmission electron microscopy and TCW show that precipitates in the Mo-containing steel are primarily M₂₃C₆, which promote pearlite formation. The experimental data also show that a lower ductility point existing in the Mo-free steel at 850°C is eliminated in the Mo-containing one. This is mainly due to the segregation of Mo at grain boundaries investigated by electron probe microanalysis (EPMA), which improves the strength of grain boundaries.     

Microstructural evolution of a heat-treated H23 tool steel

The microstructure and the stability of carbides after heat treatments in an H23 tool steel were investigated. The heat treatments consisted of austenization at two different austenizing temperatures (1100℃ and 1250℃), followed by water quenching and double-aging at 650℃, 750℃, and 800℃ with air cooling between the first and second aging treatments. Martensite did not form in the as-quenched microstructures, which consisted of a ferrite matrix, M₆C, M₇C₃, and MC carbides. The double-aged microstructures consisted of a ferrite matrix and MC, M₆C, M₇C₃, and M₂₃C₆ carbides. Secondary hardening as a consequence of secondary precipitation of fine M₂C carbides did not occur. There was disagreement between the experimental microstructure and the results of thermodynamic calculations. The highest double-aged hardness of the H23 tool steel was 448 HV after austenization at 1250℃ and double-aging at 650℃, which suggested that this tool steel should be used at temperatures below 650℃.     

The precipitation strengthening behavior of Cu-rich phase in Nb contained advanced Fe–Cr–Ni type austenitic heat resistant steel for USC power plant application

Copper has been used as a strengthening element in newly developed Fe–Cr–Ni type austenitic heat resistant steel for inducing Cu-rich phase precipitation to meet high temperature strength requirement for 60°C Ultra Super-Critical (USC) coal fired power plants for many years. However, the precipitation behavior and strengthening mechanism of Cu-rich phase in these advanced austenitic heat resistant steels is still unclear. In order to understand the precipitation strengthening behavior of Cu-rich phase and to promote high strength austenitic heat resistant steel development, 18Cr9 NiCuNb steel which is a Cu-added Nb contained advanced Fe–Cr–Ni type austenitic heat resistant steel has been selected for this study to be aged at 650°C till to 10,000 h. Micro-hardness and room temperature tensile test were conducted after long-time aging. SEM,TEM, HRTEM and three dimensional atom probe (3DAP) technology accompanying with thermodynamic calculation have been used to investigate the Cu-rich phase precipitation behavior during 650°C aging. The experimental results showed that Cu atoms can quickly concentrate in clusters at very early precipitation stage to form the fine nano-size Cu-rich ‘‘segregation areas’within less than 1 h at 650°C. With increasing aging time at 650°C Cu atoms continuously concentrate to Cu-rich segregation areas (clusters) and simultaneously other kinds of atoms such as Fe, Cr and Ni diffuse away from Cu-rich segregation areas to austenitic matrix, and finally to complete the transformation from Cu-rich segregation areas to Cu-rich phase. However, there is only Cu atoms concentration but not crystallographic transformation from early stage of Cu-rich clusters forming to the final Cu-rich phase formation. Even the Cu atom becomes the main composed element after 500 h aging at 650°C the Cu-rich phase still keeps coherent relationship with austenitic matrix. According the experimental results in this study, Cu-rich phase precipitation sequence which starts from the Cu atom segregation followed by the Cu diffusing from matrix to segregation areas and Fe, Cr and Ni atoms diffuse out from Cu-rich areas to matrix without crystallographic transformation is proposed. The Cu-rich phase is the most dispersed phase and contributes the most important strengthening effect among all precipitated phases (M23C6, MX and Cu-rich phase). It has been found that Cu-rich phase is very stable and still keeps in nano-size even for 10,000 h aging at 650°C. The unique precipitation strengthening of Cu-rich phase in combination with nano-size Nb-rich MX phase and grain-boundary M23C6carbide contributes excellent strengthening effect to 18Cr9 NiCuNb austenitic heat resistant steel.     

镍基高温合金长期时效过程中第二相的析出

为考察合金在高温长期时效过程中的组织变化情况,使合金分别在800℃,900℃进行了100～1000h的长期时效,并对由镍基基体上析出的第二相粒子利用扫描电镜、透射电镜、电子探针等测试手段进行了观察与分析·发现碳化物和TCP相的析出有着类似之处,都在800℃时效时比在更高温度时效容易析出,颗粒尺寸也大于900℃时效时的尺寸;观察到析出碳化物种类有M23C6型、M7C3型;TCP相种类有μ相、σ相·通过测量γ′相的平均半径得到其析出特性符合里夫希茨·瓦格纳的第二相粒子成熟理论·相与组织的准确确定,为其后确定合金的拉伸与持久性能提供了有力的分析基础·     

Effect of oxygen content and heat treatment on carbide precipitation behavior in PM Ni-base superalloys

The influence of oxygen content and heat treatment on the evolution of carbides in a powder metallurgy (PM) Ni-base superalloy was characterized. The results reveal that oxygen content has little influence on the precipitation of carbides inside the particles. However, under the consolidated state, stable Ti oxides on the particle surface act as nuclei for the precipitation of prior particle boundaries (PPB). Also, oxygen can diffuse internally along grain boundaries under compressive stress, which favors the precipitation of carbides inside the particles. Therefore, a higher amount of carbides will appear with more oxygen content in the case of consolidated alloys. It is also observed that PPB can be disrupted into discontinuous particles at 1200℃, but this carbide network is hard to be eliminated completely. The combined MC-M₂₃C₆ morphology approves the nucleation and growth mechanism of carbide evolution.     

过滤净化对K640S返回料力学性能的影响

对铸造钴基高温合金K640S返回合金进行过滤净化处理,测试合金化学成分、拉伸性能和蠕变性能·结果表明:过滤明显降低合金中的O、N元素的质量分数,而其他主要元素质量分数没有变化·过滤对合金拉伸性能没有明显影响·在815℃、205MPa条件下,过滤合金与未过滤合金相比,蠕变寿命从34h提高到64h·过滤后合金组织中显微疏松明显减少·可见,返回合金经过滤处理后,其性能已达到新料的性能水平·     

Effect of long-term aging treatment on the tensile strength and ductility of GH 605 superalloy

Aging treatment is an effective way to optimize the mechanical properties of Co-based superalloys. In this study, commercial GH 605 superalloy was subjected to aging treatment at 650 ?°C in a wide time range up to 1000 ?h. The effects of aging time on the tensile characteristics, microstructure evolution and mechanical properties were systematically investigated at room temperature (RT) and 900 ?°C. The results showed that the volume fractions of M₆C and M₂₃C₆ carbide increased with the aging time. After long-term aging treatment, the yield strength (YS) at RT was enhanced from 490.3 ?MPa to 805.9 ?MPa, while the alloy still had high tensile ductility (above 20%). Microscopic observations by transmission electron microscopy (TEM) indicated that the strengthening mechanism was related to carbide precipitation inside the grains and the change in the dislocation slipping mode. Moreover, long-term aging treatment can increase the elongation from 24.1% to 47.3% at 900 ?°C accompanied by a slight increase of YS from 299.3 ?MPa to 313.9 ?MPa. Based on detailed microstructure analysis the strengthening mechanism can be attributed to the refined grains as well as carbide precipitation inside the grains and around the grain boundaries.     

Kinetic study of the hydrocarbon generation from marine carbonate source rocks characterization of products of gas and liquid hydrocarbon

The kinetic parameters of hydrocarbon generation from the marine carbonate source rocks were determined and calibrated through kinetic simulating experiment. The kinetic parameters of hydrocarbon generation then were extrapolated to geological condition by using the relative software. The result shows that gaseous hydrocarbons (C_1, C_2, C_3, C_(4-5)) were generated in condition of 150℃相似文献   

钒含量对高碳高钒高速钢组织与性能的影响

对高碳高钒高速钢的显微组织、硬度及热处理工艺进行了试验研究 ,结果表明 ,其显微组织中存在有MC、M6C和M2 C型三种类型的合金碳化物 ,其中MC型碳化物起主要作用。随着含钒量的增加 ,钢中MC型碳化物数量增加 ,其形态由不连续网状向颗粒状转变。     

Carbothermal reduction process of the Fe-Cr-O system

Understanding the reduction behaviors and characteristics of the end products of Fe-Cr-O systems is very important not only for maximizing the recovery of metals from stainless steel dust but also for the subsequent reuse in metallurgical process. The present work first predicted the possible products thermodynamically when FeCr₂O₄ was reduced by C. The reduction behaviors by graphite of three kinds of Fe-Cr-O systems, i.e., FeCr₂O₄, Fe₂O₃+Cr₂O₃, and Fe+Cr₂O₃, were then investigated in 1350–1550℃. Further, the microstructures of final products and element distribution conditions were examined. The results suggest that, thermodynamically, the mass of products for the carbothermal reduction of FeCr₂O₄ is a strong function of temperature, and the initial carbon content is used. More Fe-Cr-C solution and less residual carbon content are obtained at higher temperatures and lower n_C:n_O ratios (the initial molar ratio of C to O in the sample). Experimental data show that the sample amount tends to affect the reduction rate, and the residual carbon content strongly depends on n_C:n_O. With regard to the phases present in products during the reaction process, metal carbides tend to form in the initial stage, whereas Fe-Cr-C solution forms when the degree of reduction is sufficiently high.     

电渣重熔过程冷却强度对含镁H13钢中碳化物的影响

研究电渣重熔过程冷却强度对含镁H13钢凝固组织和碳化物偏析的影响.采用光学显微镜、扫描电镜、透射电镜、X射线衍射仪等分析凝固组织及碳化物的特征.研究发现,钢锭的凝固组织均为马氏体组织、残余奥氏体及一次碳化物.H13钢电渣锭中主要析出的一次碳化物为V8C7、MC、M23 C6及M6C.随着冷却强度增加,电渣锭边部碳化物的尺寸减小且分布更加均匀,但是碳化物的类型不发生变化.电渣重熔过程中冷却强度增加促进钢中镁对夹杂物的变性能力,经过镁变性后生成的MgO· Al2O3为TiN的析出提供形核质点,MgO· Al2 O3和TiN的复合夹杂物能够促进一次碳化物异质形核,从而细化一次碳化物.     

Electroless copper-phosphorus coatings with the addition of silicon carbide (SiC) particles

Cu-P-silicon carbide (SiC) composite coatings were deposited by means of electroless plating. The effects of pH values, temperature, and different concentrations of sodium hypophosphite (NaH₂PO₂·H₂O), nickel sulfate (NiSO₄·6H₂O), sodium citrate (C₆H₅Na₃O₇·2H₂O) and SiC on the deposition rate and coating compositions were evaluated, and the bath formulation for Cu-P-SiC composite coatings was optimised. The coating compositions were determined using energy-dispersive X-ray analysis (EDX). The corresponding optimal operating parameters for depositing Cu-P-SiC are as follows: pH 9; temperature, 90℃; NaH₂PO₂·H₂O concentration, 125 g/L; NiSO₄·6H₂O concentration, 3.125 g/L; SiC concentration, 5 g/L; and C₆H₅Na₃O₇·2H₂O concentration, 50 g/L. The surface morphology of the coatings analysed by scanning electron microscopy (SEM) shows that Cu particles are uniformly distributed. The hardness and wear resistance of Cu-P composite coatings are improved with the addition of SiC particles and increase with the increase of SiC content.     

长期高温时效12Cr1MoV钢中碳化物组织结构

12Cr1MdV低合金耐热钢在540℃运行20万h后，材料中碳化物的组织结构发生显著变化．研究结果表明：材料中大量的碳化物沿晶界析出并聚集粗化，析出的碳化物主要为M23C6，同时存在少量的M6C，碳化物的沿晶界析出及其粗化是材料结构和性能发生恶化的主要原因；弥散的细小的富Ⅴ碳化物MC（V4C3）在铁素体晶体内沉淀析出，有助于12cr1MoV低合金耐热钢的性能和组织结构的稳定；珠光体组织中Fe3C发生球化和分解，但无明显聚集长大，并由原先的M3C型分解转变为MC型．     

Self-assembly of N-3-γ-pyridyl Aza[60]fulleroid on Au(111)

Self-assembled monolayers of novel C₆₀ derivative, N-3-γ-pyridyl Aza[60]fulleroid (C₆₀Py), on Au(111) were studied by a scanning tunneling microscope under ultrahigh vacuum (UHV). C₆₀Py molecules were assembled on Au (111) via pyridyl nitrogen-Au interaction. The sole assembly of C₆₀Py molecules on Au (111) only exhibited randoml aggregation of C₆₀Py even the films were annealed at 50 and 105°C. By co-assembling with benzyl mercaptan (BM), the C₆₀PyBM films showed highly dense aggregation, but C₆₀Py assemblies still had disordered structure. After the co-assembled C₆₀Py-BM films were annealed at 50°C, BM molecules were partially desorbed, but the assembly of C₆₀Py remained without obvious change. After the co-assembled C₆₀Py-BM films were further annealed at 105°C, the C₆₀Py monolayers with ordered structure were obtained, while the BM molecules were nearly thoroughly desorbed from the surface. Here, the BM molecules play a key role as a surfactant in the formation of the ordered C₆₀Py monolayer.     

In situ reaction mechanism of MgAlON in Al-Al2O3-MgO composites at 1700℃ under flowing N2

The Al-Al₂O₃-MgO composites with added aluminum contents of approximately 0wt%, 5wt%, and 10wt%, named as M₁, M₂, and M₃, respectively, were prepared at 1700℃ for 5 h under a flowing N₂ atmosphere using the reaction sintering method. After sintering, the Al-Al₂O₃-MgO composites were characterized and analyzed by X-ray diffraction, scanning electron microscopy, and energy-dispersive X-ray spectroscopy. The results show that specimen M₁ was composed of MgO and MgAl₂O₄. Compared with specimen M₁, specimens M₂ and M₃ possessed MgAlON, and its production increased with increasing aluminum addition. Under an N₂ atmosphere, MgO, Al₂O₃, and Al in the matrix of specimens M₂ and M₃ reacted to form MgAlON and AlN-polytypoids, which combined the particles and the matrix together and imparted the Al-Al₂O₃-MgO composites with a dense structure. The mechanism of MgAlON synthesis is described as follows. Under an N₂ atmosphere, the partial pressure of oxygen is quite low; thus, when the Al-Al₂O₃-MgO composites were soaked at 580℃ for an extended period, aluminum metal was transformed into AlN. With increasing temperature, Al₂O₃ diffused into AlN crystal lattices and formed AlN-polytypoids; however, MgO reacted with Al₂O₃ to form MgAl₂O₄. When the temperature was greater than (1640 ±10)℃, AlN diffused into Al₂O₃ and formed spinel-structured AlON. In situ MgAlON was acquired through a solid-solution reaction between AlON and MgAl₂O₄ at high temperatures because of their similar spinel structures.     

Zr-pillared montmoril lonite supported cobalt nanoparticles for Fischer – Tropsch synthesis

In this article Fischer–Tropsch(FT) synthesis was studied over cobalt nanoparticles supported on modifed Montmorillonite(Zr-PILC).Co-loaded/Zr-PILC catalysts were synthesized by hydrothermal methods and were characterized by XRD,XRF,BET,H2-TPR,TGA and SEM techniques.FT reactions were carried out in fxed bed microreactor(T 225 1C,260 1C and 275 1C,P 1,5 and 10 bars).The FT-products obtained over Co-loaded/Zr-PILC catalysts showed increased selectivity of C2–C12hydrocarbons and decreased selectivity towards CH4and higher molecular weight hydrocarbons(C21) at a TOS of 2–30 h as compared to the Co-loaded/NaMMT catalysts.With increase in reaction temperature from225 1C to 275 1C,CO-conversion and CH4selectivity increases while that of C5+hydrocarbons decreases.Decrease in CH4selectivity while increase in C5+hydrocarbons and CO-conversion were observed on increasing the pressure of reaction.     

Effect of sintering temperature on the preparation of Cu–Ti3SiC2 metal matrix composite

Ti3SiC2 has the potential to replace graphite as reinforcing particles in Cu matrix composites for applications in brush,electrical contacts and electrode materials.In this paper the fabrication of Cu-Ti3SiC2 metal matrix composites prepared by warm compaction powder metallurgy forming and spark plasma sintering(SPS) was studied.The stability of Ti3SiC2 at different sintering temperatures was also studied.The present experimental results indicate that the reinforcing particles in Cu-Ti3SiC2 composites are not stable at and above 800℃.The decomposition of Ti3SiC2 will lead to the formation of TiC and/or other carbides and TiSi2.If purity is the major concern,the processing and servicing temperatures of the Cu-Ti3SiC2 composite should be limited to 750℃ or lower.The composites prepared by warm compaction forming and SPS sintering at 750℃ have lower density when compared with the composites prepared by SPS sintering at 950℃,but their electrical resistivity values are very close to each other and even lower.