GCr18Mo轴承钢的下贝氏体组织转变

利用光学显微镜和透射电镜观察和分析了GCr18Mo轴承钢的下贝氏体组织形貌和精细结构,探讨了下贝氏体组织转变机理。借助于图像分析仪分析了下贝氏体转变动力学。结果表明,GCr18Mo轴承钢等温淬火后生成的下贝氏体呈针状或竹叶状,且堆聚成簇,下贝氏体中的铁素体为条状,空间呈双透镜状,由许多更小的铁素体亚条平行排列构成;GCr18Mo轴承钢的下贝氏体转变机理符合类平衡切变长大模型,其形成过程是孕育成核和快速长大的过程,它的转变动力学方程为y=1-exp(2.2×10-12t3.22)。     

长期运行后汽轮机转子裂纹扩展行为的研究

对运行16年的30Cr1Mo1V亚临界汽轮机高中压转子进行解剖试验,采用直流电位法对材料在538℃下的蠕变裂纹、蠕变-疲劳裂纹萌生与扩展行为进行了研究,分析了不同初始应力强度因子对蠕变裂纹扩展孕育时间和蠕变裂纹扩展速率的影响,并对高温段和低温段的相关性能进行了比较,研究了不同保持时间对蠕变-疲劳裂纹扩展行为的影响,同时还分析了不同条件下裂纹扩展行为的时间或循环相关性．结果表明：疲劳缩短了蠕变-疲劳裂纹的扩展孕育期,加速了裂纹的扩展;载荷保持时间较短情况下,蠕变-疲劳裂纹扩展行为与循环相关;栽荷保持时间较长情况下,裂纹扩展行为与时间相关．     

Novel Nd2WO6-type Sm2−xAxM1−yByO6−δ (A = Ca, Sr; M = Mo, W; B = Ce, Ni) mixed conductors

In the present work, we have explored novel Nd₂WO₆-type structure Sm_2−xA_xM_1−yB_yO_6−δ (A = Ca, Sr; M = Mo, W; B = Ce, Ni) as precursor for the development of solid oxide fuel cells (SOFCs) anodes. The formation of single-phase monoclinic structure was confirmed by powder X-ray diffraction (PXRD) for the A- and B-doped Sm₂MO₆ (SMO). Samples after AC measurements under wet H₂ up to 850 °C changed from Nd₂WO₆-type structure into Sm₂MoO₅ due to the reduction of Mo^VI that was confirmed by PXRD and is consistent with literature. The electrical conductivity was determined using 2-probe AC impedance and DC method and was compared with 4-probe DC method. The total electrical conductivity obtained from these two different techniques was found to vary within the experimental error over the investigated temperature of 350-650 °C. Ionic and electronic conductivity were studied using electron-blocking electrodes technique. Among the samples studied, Sm_1.8Ca_0.2MoO_6−δ exhibits total conductivity of 0.12 S cm⁻¹ at 550 °C in wet H₂ with an activation energy of 0.06 eV. Ca-doped SMO appears to be chemically stable against reaction with YSZ electrolyte at 800 °C for 24 h in wet H₂. The ionic transference number (t_i) of Sm_1.9Ca_0.1MoO_6−δ in wet H₂ at 550 °C (pO₂ = 10^−25.5 atm) was found to be about 0.012 after subtraction of electrical lead resistance from the 2-probe AC data and showed predominate electronic conductors.     

Thermodynamic investigation of phase equilibria on the (W,Mo)C-(Co,Ni) cemented carbides

The C-Co-Mo-W and C-Mo-Ni-W quaternary systems have been critically evaluated by means of the CALPHAD approach, in which the Co-Mo-W system was readjusted to ensure the model consistency. The thermodynamic models of Gibbs energies for individual phases in the ternary and quaternary systems are described, including substitutional solution model, sublattice model and linear compound model. The modeling covers the whole temperature and composition ranges, and a set of self-consistent thermodynamic parameters for the C-Co-Mo-W and C-Mo-Ni-W quaternary systems is obtained. According to the comprehensive comparisons between the reported and calculated phase diagram data, the reliable equilibria information is satisfactorily accounted for by the modeling. Based on the present work together with the previously reported assessments of binary, ternary and quaternary sub-systems, a thermodynamic database for the C-Co-Mo-Ni-W quinary system is constructed and applied to calculate the sintering region phase equilibria of the (W,Mo)C-(Co,Ni) cemented carbides.     

主产裂变99Mo研究堆的总体方案

简要分析了国际上生产⁹⁹Mo研究堆的现状和发展趋势,有针对性地提出了主产裂变⁹⁹Mo研究堆的设计理念,经初步优化设计,分析和论证了该堆的总体设计参数,给出了⁹⁹Mo产量评估和经济性分析。结果表明,该堆在保证安全性的基础上,极大地提高了生产堆的经济性。     

凝胶型99Mo-99mTc发生器研究现状

与裂变型⁹⁹Mo-^99mTc发生器相比,凝胶型⁹⁹Mo-^99mTc发生器制备^99mTc具有工艺简单、产生的放射性废物容易处理、对环境影响小等优点。本文主要论述了凝胶型⁹⁹Mo-^99mTc发生器与裂变型⁹⁹Mo-99mTc发生器的区别,堆照生产⁹⁹Mo原料和凝胶材料的研究进展,凝胶结构以及凝胶组分等多种条件因素对凝胶型⁹⁹Mo-^99mTc发生器性能的影响等,并对低比活度⁹⁹Mo生产^99mTc的研究进展进行综述。     

Preparation and mechanism of active Mo–Mn metallization on ZTA particles surface and interfacial bonding of reinforced iron matrix composite

ZrO₂ toughened Al₂O₃ particles (ZTAp) have poor wettability with iron, and therefore some defects are easily formed at the interface between ZTAp and iron matrix, which may lead to material failure. This paper illustrates that the ZTAp were modified on the surface by the active Mo–Mn metallization, and thus, they were used as the reinforcing phases to prepare the iron-matrix composite (ZTAp/Fe composite). It is concluded that the sponge-like skeleton structure was formed on the surface of ZTAp after the metallization. The interface of ZTAp/Fe composite, which has been proved to have bearing and transitional capacity by scratch test, was formed by chemical bonding with elemental diffusion, besides mechanical bonding. The metallization mechanism of elemental diffusion can be explained by the migration of glass phase, and the elements diffusion between the interface and iron matrix is to form solid solution.     

Electrochemical fabrication of Ni–Mo nanostars with Pt-like catalytic activity for both electrochemical hydrogen and oxygen evolution reactions

Synthesis of electrocatalysts with excellent performance for hydrogen and oxygen evolution are the main challenges for production of hydrogen by electrochemical water splitting method. Here, Ni–Mo nanostars were created by electrochemical deposition process at different morphologies and their electrocatalytic behavior was studied for hydrogen and oxygen evolution reactions in 1.0 M KOH solution. Increased electrochemically active surface area due to the nanostars formation, improved intrinsic electrocatalytic activity, increased surface wettability, as well as being binder-free during electrode production, resulted in excellent electrocatalytic behavior. For optimized condition, 60 mV and 225 mV overpotential are needed for generating the current density of 10 mA.cm-² in HER and OER process respectively in the alkaline medium. The lower slope of the electrode compared to the other electrodes also indicated that the kinetics of HER on the surface of the electrode was better. Also, there was very little change in the potential during the stability test, indicating the excellent electrocatalytic stability of the synthesized electrode. The present study introduces a rational, cost-effective and binder-free method for the synthesis of high performance electrocatalysts.     

Nonoxidative methane activation,coupling, and conversion to ethane,ethylene, and hydrogen over Fe/HZSM‐5, Mo/HZSM‐5, and Fe–Mo/HZSM‐5 catalysts in packed bed reactor

A high abundance of methane and its relatively low price make it an attractive raw feedstock for the production of ethylene, which is in the consumer demand in recent years. Direct catalytic nonoxidative conversion is interesting, because it could be utilized on natural gas well sites. Monometallic and bimetallic Fe and Mo catalysts were prepared for the purpose of the coupling to ethane and ethene. Three supported materials were synthesized with the following loading of metal: 2.5‐wt% Fe, 5.0‐wt% Fe, and 2.5‐wt% Mo on HZSM‐5. Process' chemical reactions were also catalyzed with a constant 2.5‐wt% Mo/HZSM‐5, which had different amounts of Fe, namely, 0.5, 1.0, and 2.5 wt%. Fourier transform infrared (FTIR), N₂ adsorption/desorption, NH₃ temperature‐programmed desorption (TPD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X‐ray diffraction (XRD) were applied for characterization. Coke, accumulated on spent solids, was determined by thermogravimetric analysis (TGA). Activity was evaluated in quartz‐packed bed reactor. All surfaces suffered from deactivation due to carbon formation. The addition of Fe to Mo increased CH₄ reacted. The highest selectivity for alkenes was achieved over 1.0‐wt% Fe to 2.5‐wt% Mo/HZSM‐5. At the peak of performance, the C‐based reactivity was 52% for olefins and 2% for alkanes. Stability was accomplished over 2.5‐wt% Fe/HZSM‐5, where the rate of C₂ synthesis was comparatively stable for 20 hours of the time on stream. The selective C‐basis yield for C₂H₄ and C₂H₆ was 36% and 23%, respectively. The lowest measured quantity of (carbonaceous) by‐products was deposited on 2.5‐wt% Fe/HZSM‐5 after 26 hours. Propylene was detected very limitedly.