Effects of Cr and Mo elements on the microstructures and compressive properties of the in situ (TiC_xN_y–TiB_2)/Ni cermets

In-situ(TiC_xN_y–TiB_2)/Ni cermets with 70 wt%TiC_xN_y–TiB_2 were successfully fabricated by combustion synthesis and hot pressing sintering in Ni-Ti-B_4C-BN powder systems.The microstructures,density,compressive properties,and hardness of the TiC_xN_y–TiB_2/Ni cermets with the addition of 0–8 wt%Cr/Mo to the Ni-Ti-B_4C-BN powder systems were compared and analysed.The results showed that the ceramic particles distributed uniformly in the cermets,and the size of the ceramic particles reduced with the Cr/Mo addition.Both Cr and Mo addition can improve the hardness,compressive properties,and fracture strains of the cermets.The hardness,compressive strength,and fracture strain of the(TiC_xN_y–TiB_2)/(Ni+Cr)cermets increased from 1561 HV,2.94 GPa,and 2.9%to 1864 HV,3.65 GPa,and 3.4%,respectively when the Cr content increased to 5 wt%.The hardness and compressive strength of the(TiC_xN_y–TiB_2)/(Ni+Mo)cermets increased from 1561 HV and 2.94 GPa to 1902 HV and 3.43 GPa,respectively when the Mo content increased to 8 wt%.The cermets with Cr had better compressive properties than the cermets with Mo.     

In situ(α-Al_2O_3+ZrB_2)/Al composites with network distribution fabricated by reaction hot pressing

In situ(α-Al_2O_3+ZrB_2)/Al composites with network distribution were fabricated using low-energy ball milling and reaction hot pressing. Differential thermal analysis(DTA) was used to study the reaction mechanisms in the Al–Zr O2–B system. X-ray diffraction(XRD) and scanning electron microscopy(SEM) in conjunction with energy-dispersive X-ray spectroscopy(EDX) were used to investigate the composite phases, morphology, and microstructure of the composites. The effect of matrix network size on the microstructure and mechanical properties was investigated. The results show that the optimum sintering parameters to complete reactions in the Al–Zr O2–B system are 850°C and 60 min. In situ-synthesized α-Al2O3 and Zr B2 particles are dispersed uniformly around Al particles, forming a network microstructure; the diameters of the α-Al2O3 and Zr B2 particles are approximately 1–3 μm. When the size of Al powder increases from 60–110 μm to 150–300 μm, the overall surface contact between Al powders and reactants decreases, thereby increasing the local volume fraction of reinforcements from 12% to 21%. This increase of the local volume leads to a significant increase in microhardness of the in situ(α-Al2O3–Zr B2)/Al composites from Hv 163 to Hv 251.     

Plasma preparation and low-temperature sintering of spherical TiC–Fe composite powder

A spherical Fe matrix composite powder containing a high volume fraction (82vol%) of fine TiC reinforcement was produced us-ing a novel process combining in situ synthesis and plasma techniques. The composite powder exhibited good sphericity and a dense struc-ture, and the fine sub-micron TiC particles were homogeneously distributed in theα-Fe matrix. A TiC–Fe cermet was prepared from the as-prepared spherical composite powder using powder metallurgy at a low sintering temperature;the product exhibited a hardness of HRA 88.5 and a flexural strength of 1360 MPa. The grain size of the fine-grained TiC and special surface structure of the spherical powder played the key roles in the fabrication process.     

Microstructural analysis and hot corrosion behavior of HVOF-sprayed Ni–22Cr–10Al–1Y and Ni–22Cr–10Al–1Y–SiC(N) coatings on ASTM-SA213-T22 steel

The present paper deals with the investigation of microstructure and high-temperature hot corrosion behavior of high-velocity oxy fuel(HVOF)-produced coatings. Two powder coating compositions, namely, Ni22Cr10Al1Y alloy powder and Ni22Cr10Al1Y(80 wt%; microsized)–silicon carbide(SiC)(20 wt%; nano(N)) powder, were deposited on a T-22 boiler tube steel. The hot corrosion behavior of bare and coated steels was tested at 900°C for 50 cycles in Na_2SO_4–60 wt%V_2O_5 molten-salt environment. The kinetics of corrosion was established with weight change measurements after each cycle. The microporosity and microhardness of the as-coated samples have been reported. The X-ray diffraction,field emission-scanning electron microscopy/energy dispersive spectroscopy, and X-ray mapping characterization techniques have been utilized for structural analysis of the as-coated and hot-corroded samples. The results showed that both coatings were deposited with a porosity less than2%. Both coated samples revealed the development of harder surfaces than the substrate. During hot corrosion testing, the bare T22 steel showed an accelerated corrosion in comparison with its coated counterparts. The HVOF-sprayed coatings were befitted effectively by maintaining their adherence during testing. The Ni22Cr10Al1Y–20 wt%SiC(N) composite coating was more effective than the Ni–22Cr–10Al–1Y coating against corrosion in the high-temperature fluxing process.     

Comparative study on the corrosion behavior of X52, 3Cr,and 13Cr steel in an O_2–H_2O–CO_2 system: products,reaction kinetics,and pitting sensitivity

The corrosion behaviors of X52, 3Cr low-alloy steel, and 13Cr stainless steel were investigated in an O_2–H2O–CO_2 environment at various temperatures and O_2–CO_2 partial-pressure ratios. The results showed that the corrosion rates of X52, 3Cr, and 13Cr steels increased with increasing temperature. The corrosion rates slowly increased at temperatures less than 100°C and increased sharply when the temperature exceeded 100°C. In the absence of O_2, X52, 3Cr, and 13Cr exhibited uniform corrosion morphology and Fe CO3 was the main corrosion product. When O_2 was introduced into the system, various forms of Fe_2O_3 appeared on the surface of the samples. The Cr content strongly influenced the corrosion resistance. The 3Cr steel with a low Cr content was more sensitive to pitting than the X52 or 13Cr steel. Thus, pitting occurred on the surface of 3Cr when 1.25 MPa of O_2 was added; this phenomenon is related to the non-uniform distribution of Crin 3Cr.     

Low-cost solid FeS lubricant as a possible alternative to MoS_2 for producing Fe-based friction materials

Three reaction systems of MoS_2–Fe, FeS –Fe, and Fe S–Fe–Mo were designed to investigate the use of FeS as an alternative to MoS_2 for producing Fe-based friction materials. Samples were prepared by powder metallurgy, and their phase compositions, microstructures, mechanical properties, and friction performance were characterized. The results showed that MoS_2 reacts with the matrix to produce iron-sulfides and Mo when sintered at 1050°C. Iron-sulfides produced in the MoS_2–Fe system were distributed uniformly and continuously in the matrix, leading to optimal mechanical properties and the lowest coefficient of friction among the systems studied. The lubricity observed was hypothesized to originate from the iron-sulfides produced. The Fe S–Fe–Mo system showed a phase composition, porosity, and density similar to those of the MoS_2–Fe system, but an uneven distribution of iron-sulfides and Mo in this system resulted in less-optimal mechanical properties. Finally, the Fe S–Fe system showed the poorest mechanical properties among the systems studied because of the lack of Mo reinforcement. In friction tests, the formation of a sulfide layer contributed to a decrease in coefficient of friction(COF) in all of the samples.     

Effect of aging temperature on the microstructures and mechanical properties of ZG12Cr9Mo1Co1NiVNbNB ferritic heat-resistant steel

The effect of aging on the mechanical properties and microstructures of a new ZG12Cr9Mo1Co1NiVNbNB ferritic heat resistant steel was investigated in this work to satisfy the high steam parameters of the ultra-supercritical power plant. The results show that the main precipitates during aging are Fe(Cr, Mo)₂₃C₆, V(Nb)C, and (Fe₂Mo) Laves in the steel. The amounts of the precipitated phases increase during aging, and correspondingly, the morphologies of phases are similar to be round. Fe(Cr, Mo)₂₃C₆ appears along boundaries and grows with increasing temperature. In addition, it is revealed that the martensitic laths are coarsened and eventually happen to be polygonization. The hardness and strength decrease gradually, whereas the plasticity of the steel increases. What’s more, the hardness of this steel after creep is similar to that of other 9%–12%Cr ferritic steels. Thus, ZG12Cr9Mo1Co1NiVNbNB can be used in the project.     

Mo含量对Ti–Mo系铁素体钢热稳定性影响

The effects of tempering holding time at 700°C on the morphology, mechanical properties, and behavior of nanoparticles in Ti–Mo ferritic steel with different Mo contents were analyzed using scanning electron microscopy and transmission electron microscopy. The equilibrium solid solution amounts of Mo, Ti, and C in ferritic steel at various temperatures were calculated, and changes in the sizes of nanoparticles over time at different Mo contents were analyzed. The experimental results and theoretical calculations were in good agreement with each other and showed that the size of nanoparticles in middle Mo content nano-ferrite (MNF) steel changed the least during aging. High Mo contents inhibited the maturation and growth of nanoparticles, but no obvious inhibitory effect was observed when the Mo content exceeded 0.37wt%. The tensile strength and yield strength continuously decreased with the tempering time. Analysis of the strengthening and toughening mechanisms showed that the different mechanical properties among the three different Mo content experiment steels were mainly determined by grain refinement strengthening (the difference range was 30–40 MPa) and precipitation strengthening (the difference range was 78–127 MPa). MNF steel displayed an ideal chemical ratio and the highest thermodynamic stability, whereas low Mo content nano-ferrite (LNF) steel and high Mo content nano-ferrite (HNF) steel displayed relatively similar thermodynamic stabilities.     

Densification behavior of mechanically milled Cu–8 at% Cr alloy and its mechanical and electrical properties

Synthesis and consolidation behavior of Cu–8 at%Cr alloy powders made by mechanical alloying with elemental Cu and Cr powders,and subsequently,compressive and electrical properties of the consolidated alloys were studied.Solid solubility of Cr in Cu during milling,and subsequent phase transformations during sintering and heat treatment of sintered components were analyzed using X-ray diffraction,scanning electron microscopy and transmission electron microscopy.The milled powders were compacted applying three different pressures(200 MPa,400 MPa and 600 MPa)and sintered in H2atmosphere at 900 1C for 30 min and at 1000 1C for 1 h and 2 h.The maximum densification(92.8%)was achieved for the sample compacted at 600 MPa and sintered for 1000 1C for 2 h.Hardness and densification behavior further increased for the compacts sintered at 900 1C for 30 min after rolling and annealing process.TEM investigation of the sintered compacts revealed the bimodal distribution of Cu grains with nano-sized Cr and Cr2O3precipitation along the grain boundary as well as in grain interior.Pinning of grain boundaries by the precipitates stabilized the fine grain structure in bimodal distribution.     

Variation in retained austenite content and mechanical properties of 0.2C–7Mn steel after intercritical annealing

The effects of annealing time and temperature on the retained austenite content and mechanical properties of 0.2C–7Mn steel were studied. The retained austenite content of 0.2C–7Mn steel was compared with that of 0.2C–5Mn steel. It is found that 0.2C–7Mn steel exhibits a similar variation trend of retained austenite content as 0.2C–5Mn steel. However, in detail, these trends are different. 0.2C–7Mn steel contains approximately 7.5vol% retained austenite after austenitization and quenching. The stability of the reversed austenite in 0.2C–7Mn steel is lower than that in 0.2C–5Mn steel; in contrast, the equilibrium reversed austenite fraction of 0.2C–7Mn steel is substantially greater than that of 0.2C–5Mn steel. Therefore, the retained austenite content in 0.2C–7Mn steel reaches 53.1vol%. The tensile results show that long annealing time and high annealing temperature may not favor the enhancement of mechanical properties of 0.2C–7Mn steel. The effect of retained austenite on the tensile strength of the steel depends on the content of retained austenite; in contrast, the 0.2% yield strength linearly decreases with increasing retained austenite content.     

Elevated-temperature properties of one long-life high-strength gun steel

The hardness, tensile strength and impact toughness of one quenched and tempered steel with nominal composition of Fe0.25C-3.0Cr-3.0Mo-0.6Ni-0.1Nb (mass fraction) both at room temperature and at elevated temperatures were investigated in order to develop high-strength steel for long-life gun barrel use. It is found that the steel has lower decrease rate of tensile strength at elevated temperature in comparison with the commonly used G4335V high-strength gun steel, which contains higher Ni and lower Cr and Mo contents. The high elevated-temperature strength of the steel is attributed to the strong secondary hardening effect and high tempering softening resistance caused by the tempering precipitation of fine Mo-rich M2C carbides in the α-Fe matrix. The experimental steel is not susceptible to secondary hardening embrittlement, meanwhile, its room-temperature impact energy is much higher than the normal requirement of impact toughness for high strength gun steels. Therefore, the steel is suitable for production of long-life high-strength gun barrels with the combination of superior elevated-temperature strength and good impact toughness.     

Effect of Mo content on the thermal stability of Ti–Mo-bearing ferritic steel

The effects of tempering holding time at 700°C on the morphology, mechanical properties, and behavior of nanoparticles in Ti–Mo ferritic steel with different Mo contents were analyzed using scanning electron microscopy and transmission electron microscopy. The equilibrium solid solution amounts of Mo, Ti, and C in ferritic steel at various temperatures were calculated, and changes in the sizes of nanoparticles over time at different Mo contents were analyzed. The experimental results and theoretical calculations were in good agreement with each other and showed that the size of nanoparticles in middle Mo content nano-ferrite(MNF) steel changed the least during aging. High Mo contents inhibited the maturation and growth of nanoparticles, but no obvious inhibitory effect was observed when the Mo content exceeded 0.37 wt%.The tensile strength and yield strength continuously decreased with the tempering time. Analysis of the strengthening and toughening mechanisms showed that the different mechanical properties among the three different Mo content experiment steels were mainly determined by grain refinement strengthening(the difference range was 30–40 MPa) and precipitation strengthening(the difference range was 78–127 MPa). MNF steel displayed an ideal chemical ratio and the highest thermodynamic stability, whereas low Mo content nano-ferrite(LNF) steel and high Mo content nano-ferrite(HNF) steel displayed relatively similar thermodynamic stabilities.     

Effect of Nb and V on the continuous cooling transformation of undercooled austenite in Cr–Mo–V steel for brake discs

The increasing speed of trains necessitates the development of brake-disc materials that meet more stringent requirements. Therefore, Nb and V have been added to Cr–Mo–V steel to improve its thermal fatigue performance when used in brake discs. In this paper, the influences of Nb and V on the static continuous cooling transformation (CCT) behaviors of undercooled austenite were studied. The microstructures, hardness, and dislocation densities at different cooling rates and with the addition of different alloying elements were also investigated. The results show that the transformation products of ferrite, granular bainite, lower bainite, and martensite form under different cooling conditions. With increasing Nb and V contents, the CCT curves are shifted to the left, ferrite and bainite transformations are promoted, and the critical cooling rate of total martensite formation is increased. The added V mainly forms V-rich M₈C₇ precipitates and reduces the dissolved C content; therefore, the A_c1, A_c3, and M_s-point temperatures increase. Moreover, the stability of retained austenite is also reduced; its content therefore decreases. Compared with V, the effect of added Nb is weaker because of its smaller content. However, the addition of Nb improves the hardness at lower cooling rates because of the precipitation of fine NbC particles and refining of the microstructure.     

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.     

High plastic Zr–Cu–Fe–Al–Nb bulk metallic glasses for biomedical applications

Four Zr–Cu–Fe–Al-based bulk metallic glasses(BMGs) with Zr contents greater than 65at% and minor additions of Nb were designed and prepared. The glass forming abilities, thermal stabilities, mechanical properties, and corrosion resistance properties of the prepared BMGs were investigated. These BMGs exhibit moderate glass forming abilities along with superior fracture and yield strengths compared to previously reported Zr–Cu–Fe–Al BMGs. Specifically, the addition of Nb into this quaternary system remarkably increases the plastic strain to 27.5%, which is related to the high Poisson's ratio and low Young's and shear moduli. The Nb-bearing BMGs also exhibit a lower corrosion current density by about one order of magnitude and a wider passive region than 316 L steel in phosphate buffer solution(PBS, pH 7.4). The combination of the optimized composition with high deformation ability, low Young's modulus, and excellent corrosion resistance properties indicates that this kind of BMG is promising for biomedical applications.     

Microstructure and mechanical properties of Nb–Mo–ZrB_2 composites prepared by hot-pressing sintering

Nb–Mo–ZrB_2 composites(V(Nb)/V(Mo) = 1) with 15 vol% or 30 vol% of ZrB_2 were fabricated by hot-pressing sintering at 2000°C. The phases, microstructure, and mechanical properties were then investigated. The composites contain Nb-Mo solid solution(denoted as(Nb, Mo)ss hereafter), Zr B, Mo B, and Nb B phases. Compressive strength test results suggest that the strength of Nb–Mo–ZrB_2 composites increases with increasing ZrB_2 content; Nb–Mo–30 vol%ZrB_2 had the highest compressive strength(1905.1 MPa). The improvement in the compressive strength of the Nb–Mo–ZrB_2 composites is mainly attributed to the secondary phase strengthening of the stiffer Zr B phase, solid-solution strengthening of the(Nb, Mo)ss matrix as well as fine-grain strengthening. The fracture toughness decreases with increasing ZrB_2 content. Finally, the fracture modes of the Nb–Mo–ZrB_2 composites are also discussed in detail.     

Microstructure evolution of T91 heat-resistant steels after long-time aging

To investigate the evolution of microstructure damage degree and the precipitated phases of heat-resistant metal in power plant under high temperature and stress environment, the high-temperature aging tests were conducted to investigate the aging behavior of T91 steel at different temperatures and stress. The optical microscopy, scanning electron microscopy, and transmission electron microscopy were used to investigate the structure and precipitated phases, the results showed that the orientation characteristics of tempered martensite was dispersed, and the grain size is obviously increased. The density of dislocation decreased with increasing temperature and stress. The important strengthening phase of M23C6 (M=Fe, Cr) was coarsened by the diffusion of main alloying elements Cr, while the smaller size MX (M=Nb,V; X=C, N) phase distributed in the grain is relatively stable in the aging.     

Thermal stability and magnetic properties of Fe–Co–M–Zr–Nb–Ge–B(M=Mo,Cr) bulk metallic glasses

Fe62Co8 xMxZr6Nb4Ge1B19(M=Mo, Cr) bulk metallic glasses were synthesized in the diameter range up to 2 mm by copper mold casting,which exhibit high thermal stability and large glass-forming ability. The super-cooled liquid region diminishes by the dissolution of Mo. The addition of 2 at% Cr leads to the broading of the liquid region remarkably, resulting in the improvement of thermal stability. The crystallization takes place through a single exothermic reaction, accompanying the precipitation of more than three kinds of crystallized phases such as α-Fe,Fe2Zr and ZrB2. The Fe-based alloys show soft ferromagnetic properties. The saturation magnetization(ss) decreases with increasing Mo or Cr content while the saturated magnetostriction increases with raising Mo or Cr content. There is no evident change in the ssand coercive force(Hc)with annealing temperature below the crystallization temperature, which suggests a more relaxed atomic configuration the glasses have. The crystallization causes a substantial enhancement in both ssand Hc. Each soft magnetic property of the glasses containing Cr with higher thermal stability is superior to that of the alloys containing Mo.     

HOVF喷涂Ni–22Cr–10Al–1Y 和Ni–22Cr–10Al–1Y–SiC (N)涂层对ASTM-SA213-T22钢组织和热腐蚀行为的影响

The present paper deals with the investigation of microstructure and high-temperature hot corrosion behavior of high-velocity oxy fuel (HVOF)-produced coatings. Two powder coating compositions, namely, Ni22Cr10Al1Y alloy powder and Ni22Cr10Al1Y (80wt%; micro-sized)–silicon carbide (SiC) (20wt%; nano (N)) powder, were deposited on a T-22 boiler tube steel. The hot corrosion behavior of bare and coated steels was tested at 900°C for 50 cycles in Na₂SO₄–60wt%V₂O₅ molten-salt environment. The kinetics of corrosion was established with weight change measurements after each cycle. The microporosity and microhardness of the as-coated samples have been reported. The X-ray diffraction, field emission-scanning electron microscopy/energy dispersive spectroscopy, and X-ray mapping characterization techniques have been utilized for structural analysis of the as-coated and hot-corroded samples. The results showed that both coatings were deposited with a porosity less than 2%. Both coated samples revealed the development of harder surfaces than the substrate. During hot corrosion testing, the bare T22 steel showed an accelerated corrosion in comparison with its coated counterparts. The HVOF-sprayed coatings were befitted effectively by maintaining their adherence during testing. The Ni22Cr10Al1Y–20wt%SiC (N) composite coating was more effective than the Ni–22Cr–10Al–1Y coating against corrosion in the high-temperature fluxing process.     

Microstructure and wear resistance of PTA clad Cr_7C_3/γ-Fe ceramal composite coating

A wear resistant Cr7C3/γ-Fe ceramal composite coating was fabricated on substrate of the hardening and tempering C degree steel by PTA (plasma transferred arc) cladding with (wt%) Fe-25Cr-7C elemental powder blends. Microstructure of the coating was characterized by OM, SEM, XRD and EDS. Wear resistance of the coating was tested under dry sliding wear condition at room temperature. The results indicate that the PTA clad ceramal composite coating has a rapidly solidified fine microstructure consisting of Cr7C3 primary particles uniformly distributed in theγ-Fe matrix and is metallurgically bonded to the C degree steel substrate. The PTA clad Cr7C3/γ-Fe ceramal composite coating has high hardness and excellent wear resistance under dry sliding wear test conditions. The excellent wear resistance of the Cr7C3/γ-Fe ceramal composite coating is attributed to the coating's high hardness, strong covalent atomic bonding and refined microstructure.