电流强度对电渣重熔304不锈钢中夹杂物特征的影响

利用实验室规模电渣炉在大气气氛下重熔304不锈钢,考察了不同电流强度(1500、1800、2100A)下电渣锭中夹杂物的特征及全氧含量、硫含量变化,并对钢中硫化物的析出行为进行了热力学分析。结果表明,电渣重熔过程可以有效去除钢中的夹杂物,但随着电流强度的增大,电渣锭的全氧含量和硫含量增加,夹杂物数密度及尺寸增大,电渣锭的洁净度恶化。当电流强度较低(1500A)时,电渣锭中夹杂物主要是以氧化铝为核心、外表裹有硫化物的双层结构,未发现单个的(Mn,Cr)S夹杂;而1800A和2100A重熔时,电渣锭中不仅有以Al-Si-Ca-Ti-Cr-Mn氧化物为核心、外围包裹着(Mn,Cr)S的双层结构夹杂,而且由于电渣锭中硫含量高和凝固过程中残余液相中溶质的富集,其中还有单个(Mn,Cr)S夹杂物存在。本试验条件下,在1500A下重熔更有利于提高304不锈钢电渣锭的洁净度。     

Effects of Zn content on the microstructure and the mechanical and corrosion properties of as-cast low-alloyed Mg–Zn–Ca alloys

The effects of Zn content on the microstructure and the mechanical and corrosion properties of as-cast low-alloyed Mg–xZn–0.2Ca alloys (x=0.6wt%, 2.0wt%, 2.5wt%, hereafter denoted as 0.6Zn, 2.0Zn, and 2.5Zn alloys, respectively) are investigated. The results show that the Zn content not only influences grain refinement but also induces different phase precipitation behaviors. The as-cast microstructure of the 0.6Zn alloy is composed of α-Mg, Mg₂Ca, and Ca₂Mg₆Zn₃ phases, whereas 2.0Zn and 2.5Zn alloys only contain α-Mg and Ca₂Mg₆Zn₃ phases, as revealed by X-ray diffraction (XRD) and transmission electron microscopy (TEM) analyses. Moreover, with increasing Zn content, both the ultimate tensile strength (UTS) and the elongation to fracture first increase and then decrease. Among the three investigated alloys, the largest UTS (178 MPa) and the highest elongation to fracture (6.5%) are obtained for the 2.0Zn alloy. In addition, the corrosion rate increases with increasing Zn content. This paper provides an updated investigation of the alloy composition–microstructure–property relationships of different Zn-containing Mg–Zn–Ca alloys.     

Microstructure and corrosion behavior of Al<Subscript>3</Subscript>Ti/ADC12 composite modified with Sr

In this study, we investigated the effect of the addition of Sr (0wt%, 0.1wt%, 0.2wt%, and 0.3wt%) on the microstructure and corrosion behavior of Al₃Ti/ADC12 composite by optical microscopy, X-ray diffraction, scanning electron microscopy, and energy diffraction spectroscopy. The results reveal that the α-Al phases were nearly spherical and 40 μm in size and that the eutectic Si phases became round in the composite when the Sr content reached 0.2wt%. The Al₃Ti particles were distributed uniformly at the grain boundary. The results of the corrosion examination reveal that the Al₃Ti/ADC12 composite exhibited a minimum corrosion rate of 0.081 g·m–2·h–1 for an Sr content of 0.2wt%, which is two thirds of that of unmodified composite (0.134 g·m–2·h–1). This improved corrosion resistance was due to galvanic corrosion, which resulted from the low area ratio of the cathode to anode regions. This caused a low-density corrosion current in the composite, thereby yielding optimum corrosion resistance.     

Preparation and performance of a cold gas dynamic sprayed high-aluminum bronze coating

By mixing preheated high-aluminum bronze powders with different amounts of Al₂O₃ powder, a low-pressure cold-sprayed coating was prepared and sprayed onto a Cr12MoV steel substrate. The hardness of the coating and the bonding strength between the coating and the substrate were tested with a HV-1000 microhardness tester and a mechanical universal testing machine. The surface microstructure, cross-section and tensile fracture surface of the coating were observed with a scanning electron microscope (SEM). Correspondingly, the influences of the preheat treatment temperature of the bronze powder and the Al₂O₃ content on the coating performance were investigated. The results indicate that the hardness of bronze powders decreased and the coating deposition rate increased after the preheating treatment of the bronze powder. The Al₂O₃ content in the mixed powders contributed to the deformation of bronze powders during the spraying process. This trend resulted in varied performance of the coating.     

Corrosion behavior of high-strength spring steel for high-speed railway

The corrosion resistance and evolution of corrosion products in medium-carbon high-strength spring steels were investigated in a neutral salt spray (5wt% NaCl solution). A formation model of γ-FeOOH and a transformation model describing the conversion of γ-FeOOH to α-FeOOH were constructed. The results indicated that, at the initial corrosion stage, the corrosion resistance was gradually improved with the addition of Cr; however, with the addition of alloying element V, the corrosion resistance decreased. These results were attributed mainly to the initial corrosion stage being closely related to the matrix microstructure parameters such as grain-boundary character and dislocation density. After the rust layer was formed at a later corrosion stage, the corrosion resistance was reinforced with the addition of Cr and V because Cr strongly influenced the composition, structure, and morphology of the corrosion products. The results presented herein show that Cr was conducive to the transformation of γ-FeOOH into α-FeOOH. Moreover, V and Cr exhibited obvious synergy and were enriched in the inner layer of the corrosion products.     

Improvement of microstructure and corrosion properties of friction stir welded AA5754 by adding Zn interlayer

This study investigated the effect of Zn foil layers on the microstructure and corrosion characteristics of friction stir welded aluminum alloy 5754. Samples of various joints were prepared by applying different rotational and welding speeds, and their microstructures were evaluated via a metallographic technique and scanning electron microscopy equipped with energy-dispersive X-ray spectroscopy elemental analysis. The anticorrosion behavior of joints in the absence and presence of a Zn interlayer was studied by cyclic potentiodynamic polarization test in 3.5wt% NaCl aqueous solution, and sound welds were obtained in the presence of the Zn interlayer foil. The results revealed that the joint made at a rotational speed of 800 r/min and traveling speed of 15 mm/min achieved a chemical composition identical to that of aluminum alloy 7xxx series, and as such, it showed the best resistance to corrosion.     

Process mineralogy characteristics of acid leaching residue produced in low-temperature roasting-acid leaching pretreatment process of refractory gold concentrates

To provide a theoretical basis for a suitable process to extract gold from refractory gold concentrates, process mineralogy on the acid leaching residue of gold calcine was studied by chemical composition, X-ray diffraction, scanning electron microscopy-energy spectrum, and mineral dissociation analysis. The results showed that the acid leaching residue contained Au 68.22 g/t, Ag 92.71 g/t, Fe 0.44%, As 0.10%, and S 0.55%. Gold and silver minerals existed as native gold, argentite, and proustite. Quartz, the main gangue mineral, accounted for 78.33wt/%. The dissociation degree analysis showed that the proportions of monomer and exposed gold in acid leaching residue were 96.66wt%. The cyanidation results showed that the cyanide gold leaching rate of acid leaching residues was close to 100wt%. However, the maximum cyanide gold leaching rate of gold calcine was only 85.31wt%. This suggests that acid leaching can increase the gold dissolution rate in the cyanide process.     

Effect of Ce addition on microstructures and mechanical properties of A380 aluminum alloy prepared by squeeze-casting

The effect of cerium (Ce) addition on the eutectic Si, β-Al₅FeSi phase, and the tensile properties of A380 alloy specimens prepared by squeeze-casting were studied by optical microscopy (OM), scanning electron microscopy (SEM), and X-ray diffraction (XRD). The experimental results showed that Ce more effectively modified the eutectic Si and refined the β-Al₅FeSi. The refinement effect significantly increased under a specific pressure of 100 MPa with the addition of Ce from 0.1wt% to 0.9wt%. In contrast, the average length and the aspect ratio of the eutectic Si and β-Al₅FeSi exhibited their optimal values when the content of the added Ce was greater than 0.5wt%. Needle-like Al8Cu4Ce was precipitated with the addition of excessive Ce; hence, the mechanical properties of A380 gradually decreased with increasing Ce content in the range from 0.3wt% to 0.9wt%.     

Complementation in the composition of steel slag and red mud for preparation of novel ceramics

A method for preparing novel ceramics was developed in this study. Different ratios red muds were added to steel slags to optimize the preparation of novel ceramics by a traditional ceramic preparation process. The sintering mechanism, microstructure, and performance were studied by X-ray diffraction techniques, scanning electron microscopy, and combined experiments of linear shrinkage, water absorption, and flexural strength. The results confirmed that red mud can reduce the volumetric instabilities through the complementarity of red mud and ferroalloy slag. The crystal phases in the ceramics are all pyroxene group minerals, including diopside ferrian, augite, and diopside. The flexural strength of the ceramic that contains 40wt% red mud and was prepared at the optimal sintering temperature (1140℃) is greater than 93 MPa; its corresponding water absorption is less than 0.05%.     

Leaching behavior of V,Pb, Cd,Cr, and As from stone coal waste rock with different particle sizes

This paper investigates the leaching behavior of heavy metals (V, Pb, Cd, Cr, and As) from stone coal waste rocks with various particle sizes using dynamic leaching experiments. The results show that the dissolved concentrations of V and As initially increased and then slightly decreased as time progressed and that the dissolved concentrations of Pb, Cd, and Cr were high in the early stage before decreasing. The particle size of the stone coal waste rocks strongly influenced the heavy metal concentration in the leaching solutions. The effects of the particle size of the stone coal waste rocks on the dissolved concentrations of V, Pb, and As decreased in the order fine fraction > medium fraction > coarse fraction, and the effects of particle size on the dissolved concentrations of Cr and Cd decreased in the order medium fraction > coarse fraction > fine fraction and coarse fraction > medium fraction > fine fraction, respectively. The quantities of heavy metals dissolved from the stone coal waste rock with fine particle sizes were observed to decrease in the order V (17104.36 μg/kg) > As (609.41 μg/kg) > Pb (469.24 μg/kg) > Cr (56.35 μg/kg) > Cd (27.52 μg/kg), and the dissolution rates decreased in the order As (2.96%) > Pb (0.93%) > V (0.35%) > Cd (0.25%) > Cr (0.01%). The specific surface area, pore size of the stone coal waste rocks, and chemical forms of heavy metals also influenced the release of heavy metals from the stone coal waste rocks. Kinetic analysis showed that the dissolution of heavy metals fundamentally agreed with the rate equation controlled by the shrinking core model. The results of this study are expected to serve as a reference for the evaluation of heavy metals contamination from stone coal waste rocks.