耐腐蚀摩托艇ADC12-0.5La铝合金微观组织及制备

为改善ADC12铝合金的耐腐蚀性能,通过超声熔铸法制备ADC12-0.5La铝合金,并利用光学显微镜、扫描电镜、能谱分析仪、硬度计、浸泡腐蚀试验和电化学工作站研究了T6热处理和稀土La改性对ADC12铝合金的微观组织、硬度和耐腐蚀性能的影响。结果表明,T6态ADC12-0.5La铝合金微观组织明显细化,α-Al尺寸减小,形貌变圆整,共晶Si相和AlFeMnSi相细化为短棒状。相比于ADC12铝合金,T6态ADC12-0.5La铝合金硬度达到117.7HV,提高了26.8%,腐蚀电流密度降低了10.7%,腐蚀电位上升了64.4%,腐蚀速率降低了54.4%,腐蚀表面平坦且光滑,表现为较轻微的晶间腐蚀。T6态ADC12-0.5La铝合金提高了腐蚀电位,Al-La-Cu稀土相阻碍了电子移动,铝合金的耐腐蚀性能得到大幅度提高。     

Catalytic ozonation of NH4+-N in wastewater over composite metal oxide catalyst

Large amounts of water containing-ammonium nitrogen(NH₄⁺-N)have attracted increasing attention.Catalytic ozonation technology,involving the generation of hydroxyl radical(OH)with strong oxidation ability,was originally utilized to degrade organic-containing wastewater.In this paper,Ce/MnOx composite metal oxide catalysts prepared with different preparation conditions were used to degrade wastewater containing inorganic pollutant(NH₄⁺-N).The as-prepared catalyst features were characterized using X-ray diffraction(XRD),Brunauer-Emmett-Teller method(BET),scanning electron microscopy(SEM),energy dispersive X-ray spectroscopy(EDS),Fourier transform infrared spectroscopy(FTIR),X-ray photoelectron spectroscopy(XPS)and H₂-temperature programmed reduction(H₂-TPR)techniques.The results show that the catalyst,prepared by conditions with precipitant Na₂CO₃ and Ce/Mn molar ratio 1:2 calcined at 400℃for 3 h in pH 11.0,displays the optimal performance,with the removal rate of NH₄⁺-N and selectivity to gaseous nitrogen,88.14 wt%and 53.67 wt%,respectively.The effects of several operating factors including solution pH,initial NH₄⁺-N concentrations and scavengers were evaluated.In addition,XRD patterns of catalyst with the best performance and the comparative study on decontamination of NH₄⁺-N by various processes(O₃,catalyst and catalyst/O₃)show that the primary metal oxides are CeO₂ and MnO₂ in Ce/MnOx composite metal oxide catalysts,which have a synergistic effect on the catalytic ozonation of NH₄⁺-N,and the new phase MnO₂ plays a great role.After 5 consecutive use cycles,the degradation efficiency is declined slightly,and can still achieve better than 70 wt%over 1 h reaction.Additionally,the application of catalytic ozonation for actual wastewater on the removal rate of NH₄⁺-N was investigated.Possible mechanism and degradation pathway of NH₄⁺-N were also proposed.In a word,the application of CeO₂-MnO₂ composite metal oxide catalysts in catalytic ozonation can be regarded as an effective,feasible and promising method for the treatment of NH₄⁺-N.     

Stable NiO–CeO2 nanoparticles with improved carbon resistance for methane dry reforming

High surface area mixed oxide 8.7% NiO-CeO₂ nanoparticles (122 m²/g; 6–7 nm) were prepared using a reversed microemulsion method, and were tested for dry methane reforming (DRM). The catalytic activity of these nanoparticles remains stable under the severe conditions of DRM (700 °C), and they show better carbon resistance than conventional NiO-CeO₂ catalysts prepared without control of the size. The activity and selectivity of nanoparticles and reference catalyst are similar, but nanoparticles reduce the accumulation of carbon by 63% during the DRM tests, which is a key feature for this reaction. XPS and H₂-TPR suggest that the improved carbon resistance of the nanoparticles is due to the better interaction and cooperation between NiO and CeO₂ mixed phases. In nanoparticles, the participation of cerium cations in the redox processes taking place during DRM stabilizes cationic species of nickel. On the contrary, the catalyst prepared without control of the size suffers segregation of Ni during DRM reaction, and segregated Ni explains the higher catalytic formation of carbon.     

化合物TbMn6Sn6的磁性和磁相变

采用分子场理论模型对稀土-过渡族金属间化合物的磁性、自旋重取向相变和场诱导的一级磁相变进行了研究.从理论上计算了TbMn6Sn6的易磁化方向随温度的变化以及不同温度时的磁化曲线,描述了自旋重取向相变和场诱导的一级磁相变.基于单离子模型计算了Tb离子和化合物的一阶和二阶磁晶各向异性常数及其随温度的变化,得到了和实验数据基本一致的结果.结果表明:Mn次晶格和Tb次晶格磁晶各向异性能之间的相互竞争是导致自旋重取向相变的物理机制,而稀土离子的四阶晶场项对场诱导的一级磁相变产生很大的影响.     

Structure, magnetization, and magnetostriction of Sm-R-Fe （R = Pr, Nd） thin films

The structure, magnetization, and magnetostriction of Sm0.9Pr0.1Fex and Sm1-xNdxFel.9 thin films have been investigated using X-ray diffraction, vibrating sample magnetometer, and optical cantilever method. It is found that the structure of Sm0.9Pr0.1Fex thin films consists of an Sm-Pr-Fe amorphous phase when x≤2.69 and that of Sm1-xNdxFel.9 thin films consists of an Sm-Nd-Fe amorphous phase. The in-plane magnetization of Sm0.91Pr0.1Fex thin films increases with increase in the Fe content, and low values of the in-plane coercivity occur in the range of 1.62≤ x≤ 2.28. The magnetostriction value of Sm0.91Pr0.1Fex thin films increases with increasing the Fe content when x ≤ 1.94 and decreases when x 〉 1.94. The in-plane magnetostriction of Sm1-xNdxFe1.9 thin films under low magnetic fields has been improved by the substitution of Nd for Sm when x = 0.2.     

A1-Li合金的拉伸断裂过程研究

以2090 Ce合金为研究对象，对不同时效时间的室温拉伸断口进行了半定量分析，探讨了拉伸性能对断裂特征的响应关系，重点分析合金分层裂纹的形成过程。研究表明：2090 Ce合金的断裂方式以韧窝、分层开裂和沿亚晶界开裂3种为主，随时效时间的延长，韧窝、分层开裂逐渐减少，沿亚晶界开裂比例逐渐加大：分层开裂程度与时效程度有密切关系：分层开裂过程与试样内部受力状态、晶界状态有密切关系。分层最先发生在试样中心，随后在二分之一、四分之一……处反复发生，最终将试样分割成一系列平行的薄板。时效后期由于亚晶界的弱化，使裂纹倾向沿亚晶界扩展，从而抑制分层开裂的发生，同时导致合金强度，尤其是塑性的下降。     

采用稀土贮氢材料的镍氢电池

介绍了镍-金属氢化物电池的特性和该类电池所用的稀土贮氢材料及其成份配制、制备工艺、合金添加剂对LaNi_5基合金电极综合性能的影响,以及该类电池的应用开发前景。     

模具盐浴稀土钒硼共渗的组织与性能

研究了Ｃｒ１２Ｍｏｖ．Ｃｒ１２，９ＣｒＳｉ和Ｔ８等钢的盐浴稀土钒硼共渗共艺，渗层组织与性能；讨论了共渗工艺参数、共渗剂成分配比及稀土元素添加量等因素对共渗层的影响。冷作模具的使用寿命经ＲＥ－Ｖ－Ｂ共渗处理后比常规工艺处理的提高３～７倍。     

萃取预分离法分离富铕中钇矿新工艺

采用一种新的串级萃取方式--萃取预分离法分离富铕中钇矿的新工艺.原料首先流入十几的三出口预先粗分离工艺,其萃余液La～Gd(TbDy)直接流入Nd/Sm工艺;中间出口流入(Gd)Tb～HoY(Er)Gd～Dy/Ho～LuY细分离工艺;出口负载有机相(Ho)Er～LuY流入Gd～Dy/Ho～LuY的洗涤段.结果表明,新工艺的粗分离工艺将占原料约70%的La～Gd(TbDy)预分离掉,使流入Gd～Dy/Ho～LuY工艺的稀土量减少约70%;由于Gd～Dy/Ho～LuY分组的萃余液GdTbDy含Ho2O3小于0.03%,省去原工艺的GdTbDy/HoY分离;新工艺的处理能力提高30%,酸碱消耗减少20%以上,贵重稀土元素Eu和Tb的存槽量大大减少.     

铝合金变质处理的现状和发展趋势

本文主要叙述了铝合金变质处理的方法及特点,并对铝合金变质方法的发展趋势作了展望.