La1-xSrxCo1-yFeyO3材料制备及结构分析

以溶胶-凝胶法制备La1-xSrxCo1-yFeyO3粉体,对粉体在不同温度热处理后的晶体结构进行XRD表征,详细研究粉体的成分组成以及发生的结构转变.结果表明,凝胶前驱体粉体颗粒比表面增大有利于钙钛矿结构晶相形成;合成粉体受前驱体比表面程度影响形成两种具有不同空间群钙钛矿结构晶相,并且各晶相元素化学计量比不相同,两相体系较稳定.     

Microstructures and properties of Sn-Ag-Cu lead-flee solder alloys containing La

Trace amounts of La were utilized to improve the melting behaviors, microstructures, tensile properties and microhardness of Sn-3.0Ag-0.5Cu lead-free solder alloy. La has little effect on the melting behavior of Sn-3.0Ag-0.5Cu alloy according to the differential thermal analysis （DTA） tests. The X-ray diffraction （XRD） patterns show that β-Sn, Ag3Sn and Cu6Sn5 coexist in the as-cast solder alloys and LaSn3 phases emerge when adding 0.4% La. The microstructures modified by La are more uniform and much finer than that of baseline alloy, and the coarse LaSn3 particles with complex dendrites are observed by optical microscopy （OM） and scanning electron microscopy （SEM） when the addition of La is up to 0.4%. The composition of the LaSn3 phases is identified by energy-dispersive spectroscopy （EDS）. There are considerable improvements in mechanical properties with 0.05% and 0.1% addition, but degenerations by adding 0.4%La. The Vickers microhardness of β-Sn and eutectic area are both enhanced with the addition of La and the microhardness of LaSn3 is much larger than those of β-Sn and eutectic area.     

稀土对ZAlSi12Cu2Mg1陶瓷层性能的影响

通过在Na2SiO2电解液体系中同时添加0．2g／L的Ce^3＋和不同含量的La^3＋以调整电解液组成，研究了Na2SiO3电解液中添加稀土离子对ZAlSi12Cu2Mg1合金微弧氧化陶瓷层相结构和力学性能的影响。结果表明，电解液中添加Ce^3＋和La^3＋，可以显著提高陶瓷层质量，其中添加0．2g／L的Ce^3＋和0．3g／L的La^3＋，所得陶瓷层主要由α—Al2O3、γ-Al2O3、Al2SiO3和非晶相组成，陶瓷层厚为157μm，硬度（HV）为947，经6000r磨损后，ZAlSi12Cu2Mg1合金基体的磨损量为102．2mg，而陶瓷层S1磨损量为19．7mg，仅为铝合金基体的19％。     

热处理对La0．7Mg0．3Ni2．8Co0．5贮氢合金电化学性能的影响

La0．7Mg0．3Ni2．8Co0．5贮氢电极合金经过适当热处理后(1123K)，最大放电容量、循环稳定性、高倍率放电性能(HRD)、交换电流密度(I0)以及极限电流密度(IL)都有明显改善，铸态合金电极的最大放电容量为392mAh／g，放电电流密度，Id=2000mA／g时，HRD2000=74．0％，I0=266．7mA／g，IL=3425．5mA／g；经1123K保温8h退火的合金电极的最大放电容量提高到414mAh／g，HRD2000=76．2％，I0=407．9mA／g，IL=3753．6mA／g。X射线衍射(XRD)分析表明，衍射峰宽度随着退火温度的升高而变窄，其原因是合金经退火处理相结构的变化和成分的均匀化。     

La2O3-Gd2O3-Mo secondary emission material

A new kind of materials La2O3-Gd2O3-Mo has been produced by powder metallurgy method.The composition and microstructure of the material were studied by XRD and SEM.It shows that no chemical reaction takes place among La2O3,Gd2O3,Mo and the rare earth oxides exist along molybdenum grain boundaries and in the pores.The emission property measurement results of this material show that adding rare earth oxide into molybdenum can improve the secondary emission coefficient of the emitter,and the emission property depends on the activation temperature.After La2O3-Gd2O3-Mo was activated at 1360℃,the maximum secondary emission coefficient can be high to 2.62,which has exceeded that for practical uses(2.0).     

含La医用316L不锈钢在生理盐水中的腐蚀行为

利用阳极极化曲线研究了含La医用316L不锈钢在37℃生理盐水中的腐蚀行为.结果表明:La含量对316L不锈钢的耐蚀性具有重要影响,随La含量降低,极化曲线的钝化区变宽,钝化电流密度则基本维持在同一水平.当含La医用316L不锈钢中La含量为0.04mass%时,其耐蚀性与医用316L相当,La含量为0.01mass%时,其耐腐蚀性最好,而La含量为0.08mass%时,其耐蚀性最差.含La医用316L不锈钢在生理盐水中的腐蚀行为主要源于La元素影响其钝化膜的形成.     

La0．67Mg0．33Ni2．5Co0．5贮氢合金的制备和MH电极性能研究

采用高频感应熔炼方法制备了PuNi3型La0.67Mg0.33Ni2.5Co0.5合金;用X射线衍射分析和电化学方法研究了添加不同Mg含量以补偿Mg元素烧损时合金的组织结构和电化学性能。X射线衍射分析(XRD)表明,铸态合金由．PuNi3型主相和少量的CaCu5型第二相组成,铸态合金经1223K和10h退火处理后,CaCu5型第二相可明显减少,其中Mg增加10％时得到纯度较高的PuNi3型组织。电化学测试表明,增加适当Mg含量和进行退火热处理能明显提高和改善合金电极容量、循环稳定性和大电流放电性能。与AB5型和。482型Laves相贮氢合金比较,PuNi3型La0.67Mg0.33Ni2.5Co0.5贮氢合金具有电极容量高及优良的大电流放电性能。     

Chemical control of superconducting properties of (Y, Ca)(Sr, Ba)2Cu2.7Ga0.3O7?δ

The partial substitution of Ga at the Cu(1) (chain) sites of the YBa₂Cu₃O₇ structure allows synthesis at ambient pressure of Ba-free analogs, e.g., YSr₂Cu_2.7Ga_0.3O_7– . Materials with this composition have been found to be nonsuperconducting, but superconductivity has been induced by one or more of the following methods: Ca substitutions at the Y site; Ba substitutions at the Sr site; annealing in high-pressure oxygen. The influence of these chemical manipulations onT _c has been monitored and all methods have been found to enhanceT _c . The electronic effects of Ba substitutions have been deduced indirectly using powder neutron diffraction, and such substitutions appear to result in a redistribution of hole density into the Cu(1) sites from the superconducting CuO₂ planes.     

Single-crystal growth and anisotropic electrical properties of (La1?xCax)2CaCu2O6

Large single crystals of (La_1–x Ca _x )₂CaCu₂O₆ were synthesized by the travelling solvent floating zone (TSFZ) technique. The dimension of the grown boules was typically 4 mm×30 mm long with thec-axis perpendicular to the growth direction. After oxygen loading at 1080°C in 400 atm of O₂, they became superconductive with a sharp transition at around 50 K. The resistivity was metallic both along thec-axis and within theab-plane, with an anisotropy ratio of ²( _c/ _ab ) 50 which is almost independent of temperature. Details of the crystal growth, heat treatment procedures, and the results of electrical and magnetic property measurements are presented.     

Synthesis, composition, and structure of superconducting (Y, Ca)Sr, Ba)2Cu2GaO7?δ

The superconducting properties of Y_1–y Ca _y Sr₂Cu₂GaO_7– have been examined and related to the Ca content,y, and the use of annealing treatments at 350 bar oxygen. Superconductivity withT _c up to 41 K was found only for high-pressure-annealed samples, and the structural effects of Ca substitution and high-pressure treatment were examined using powder neutron diffraction. Small but significant changes in Cu-Cu and Cu-O distances were found and suggest that the Cu ions are more highly charged in superconducting samples. Partial substitution of Ba for Sr was found to be possible (up to 20%) to give samples which, after annealing in high-pressure oxygen, were superconducting at temperatures up to 68 K.