In-situ observation of interaction between precipitates and austenite during δ→γ phase transformations

The δ-ferrite to γ-austenite phase transformation in duplex stainless steels was observed using ultra high-temperature confocal laser scanning microscope, and the orientation relationship between the γ phase, and precipitate is discussed. Owing to mutual promotion action, the γ phase was observed at δ/δ grain boundary at the beginning of δ-ferrite→γ-austenite transformation, followed by two-dimensional γ-phase growth at the same speed (0.625?µm?s^?1) along the grain boundary and into the δ grain matrix. The γ-phase growth rate decreases to 0.244?µm?s^?1 when precipitate stops growing. In the process of grain growth at high temperature, the precipitated pinning grain boundary will slow the movement speed of the grain boundary.

The mutual promotion action leads to preferential nucleation of the γ phase, and the nucleation and growth of the austenite also promoting the growth of MnS the growth.     

Methods for constructing analytic phase function for small spherical particle polydispersions

Two ways of constructing analytic phase function for a polydispersion of small spherical non-absorbing particles have been investigated. First one is a straightforward procedure emanating from the implementation of single particle scattering input into the defined polydisperse phase function. This results in an analytic phase function in terms of moments of the distribution. The second approach is a new strategy, based on the Lagrange mean value theorem. A clear understanding of the relationship between these two approaches has been developed. The efficacy and accuracy of the scattering phase functions is illustrated by applying it to a power-law size distributed sphere ensemble.     

不锈钢酸洗污泥对烧结黏结相与平衡相的影响

 不锈钢酸洗污泥安全填埋占用土地且难以消除对环境的危害，将酸洗污泥作为烧结配料使用有望回收其中铁、铬、镍等金属，并充分利用其中的熔剂组分，实现酸洗污泥在冶金企业的闭路资源化利用。铁矿粉配加酸洗污泥烧结黏结相强度试验表明，随着酸洗污泥配加比例的增加，黏结相强度先增加后减小，且随着碱度的增加整体减小，当酸洗污泥配加比例为10%时，试样中赤铁矿、磁铁矿质量分数最大，枪晶石质量分数较小，在碱度为1.5时于1 280 ℃焙烧4 min，试样的黏结相强度最大可达15.12 kN。平衡相烧结试验表明，配加酸洗污泥能改善烧结矿质量，铁矿粉配加10%的酸洗污泥，碱度为1.5，1 300 ℃烧结240 min后，烧结矿的矿相组成和微观结构最好，综合性能最佳。     

云南镇源难处理金精矿工艺矿物学研究

利用X射线衍射、X射线荧光光谱（XRF）、X射线能谱分析（EDX）和矿物解离分析（MLA）等检测手段对云南镇源难处理金精矿的化学组成、矿物组成、硫化物特征以及金的分布情况进行了详细的工艺矿物学研究。结果显示：该金矿以硫化矿、碳酸盐和硅酸盐类矿物为主，含有3.18%的有机碳和2.37%的无机碳。通过金的诊断浸出发现96.16%的金被硫化物包裹，少量金以单体形式存在。通过对主要载金矿物黄铁矿、辉锑矿和毒砂的粒度、包裹及裸露情况进行分析，得出大部分硫化矿以解离单体的形式存在，少部分与其他矿物共生。根据MLA测试及金的诊断浸出，认为大部分金被硫化矿完全包裹，处理该矿石时应先进行硫化物包裹层的氧化处理，再进行金矿的浸出。     

Hydrogen embrittlement and associated surface crack growth in fine-grained equiatomic CoCrFeMnNi high-entropy alloys with different annealing temperatures evaluated by tensile testing under in situ hydrogen charging

The effect of the annealing temperature after cold rolling on hydrogen embrittlement resistance was investigated with a face-centered cubic (FCC) equiatomic CoCrFeMnNi high-entropy alloy using tensile testing under electrochemical hydrogen charging. Decreasing annealing temperature from 800 °C to 750 °C decreased grain sizes from 3.2 to 2.1 μm, and resulted in the σ phase formation. Interestingly, the specimen annealed at 800 °C, which had coarser grains, showed a lower hydrogen embrittlement susceptibility than the specimen annealed at 750 °C, although hydrogen-assisted intergranular fracture was observed in both annealing conditions. Because the interface between the FCC matrix and σ was more susceptible to hydrogen than the grain boundary, the presence of the matrix/σ interface significantly assisted hydrogen-induced mechanical degradation. In terms of intergranular cracking, crack growth occurred via small crack initiation near a larger crack tip and subsequent crack coalescence, which has been observed in various steels and FCC alloys that contained hydrogen.     

基于BS值的钢中多相组织分相技术

为了对钢中双相或多相组织进行分相定量表征，利用场发射扫描电镜(FE SEM)与电子背散射衍射技术(EBSD)中的BS值对其进行了详细的研究与讨论。结果表明，对于单相的铁素体、贝氏体或马氏体，其BS灰度分布图呈近似的正态分布，BS图可以呈现出类似于组织的图像。利用BS值可以很好地对结构相近的双相或多相组织进行分相定量。在分相定量时，需选择适合的拟合函数，定量结果才更为准确。     

Maximization of quadruple phase boundary for alkaline membrane fuel cell using non-stoichiometric α-MnO2 as cathode catalyst

Oxygen can only be reduced at the quadruple phase boundary (catalyst, carbon support, ionomer and oxygen) of the cathode catalyst layer with non-conducting electrocatalyst. To maximize the quadruple phase boundary sites is crucial to increase the peak power density of each membrane electrode assembly. The quadruple phase boundary is depending on the ratio of catalyst, carbon support and ionomer. The loading of catalyst layer is also crucial to the fuel cell performance. In this study, non-stoichiometric α-MnO₂ manganese dioxide nanorod material has been synthesized and the ratios of carbon, ionomer and catalyst loadings were optimized in alkaline membrane fuel cell. In total, ten membrane electrode assemblies have been manufactured and tested. Taguchi design method has been applied in order to understand the effect of each parameter. The conclusion finds out the ionomer has more influence on the alkaline membrane fuel cell peak power performance than carbon and loading.     

Structural transformation in Mn-substituted Sr2Bi2Ta2TiO12 Aurivillius phase synthesized by hydrothermal method: A comparative study and dielectric properties

In this study, a hydrothermal method was applied to synthesize the three-layer Aurivillius phase Sr₂Bi₂Ta₂TiO₁₂ (SBTTO) and Mn-substituted Sr_1·5Bi_2·5Ta₂Ti_0·5Mn_0·5O₁₂ (SBTTMO), with the use of NaOH as a mineralizer. The crystal structure, morphology, dielectric properties, and the correlation between the structural transformation and dielectric properties were investigated. The XRD data reveal that the SBTTO sample adopts a tetragonal crystal structure with the I4/mmm space group and is then transformed into an orthorhombic structure with the B2cb space group for SBTTMO. The morphology of both samples was observed by SEM, which showed anisotropic plate-like grains. With the Mn substitution, the ferroelectric transition temperature (T_c) significantly increases as the influence of the 6s² lone pair of Bi³⁺ increases, and this in turn further induces the relaxor-ferroelectric behavior. Consequently, the increase in T_c confirms the structural transformation from the paraelectric-tetragonal to the ferroelectric-orthorhombic phase.