电解电容器铝箔纯交流腐蚀工艺影响因素的研究

对电解电容器铝箔交流腐蚀体系中各影响因素的研究结果表明，在电流密度为０．５Ａ／ｃｍ２，温度为４７±２℃；控制腐蚀液中Ａｌ（３＋）含量及适量添加表面保护剂和辅助添加剂的条件下，可获得最大比电容。通过循环伏安曲线测试，探讨了各因素影响腐蚀的机理及相互关系。     

LiFePO4基正极材料容量的温度敏感特性及交流阻抗谱研究

采用原位碳包覆法制备了锂离子二次电池用LiFePO4／C复合正极材料。考察了环境温度对LiFePO4/C电池容量的影响，得到容量与绝对温度之间符合Arrhenius关系。运用交流阻抗谱分析了温度与电池电化学特性的关系，并对电极基于电荷和质量传递控制过程给出了一种新的模拟等效电路，通过Zview拟合软件得到了各个模拟元件的数值及变化趋势，从而定量地解释LiFePO4／C复合电极容量与温度的关系。     

交流方波氩弧焊功率变换器

本文提出一种用于交流氩弧焊的功率变换器,它与具有陡降特性的直流焊接电源配套进行交流方波氩弧焊。文中介绍了其工作原理,性能特点及主要研究设计内容。结果表明,该方法是实现高质量交流氩弧焊的有效途径之一。     

交流TIG电弧粉末堆焊层成形特点的研究

为了降低TIG电孤堆焊时因直流正接造成堆焊金属稀释率过大的问题，尝试使用交流TIG电弧进行粉末堆焊，研究了堆焊层的成形特点。实验表明，与直流正接相比．使用相同电流值的交流TIG电弧进行粉末堆焊，获得的堆焊层熔宽更大．熔深和母材熔化量更小．因而具有更小的深宽比和稀释率。这一规律不随堆焊电流的大小和堆焊材料的不同而发生变化．     

Synthesis and electrochemical properties of Th-doped LiMn2O4 powders for lithium-ion batteries

To improve the cycle performance of eco-friendly and cost-effective spinel LiMN2O4 as the Li secondary batteries, the Th-doped LiThxMn1-xO4 spinel powers were synthesized by solid-state method. The starting materials, Li2CO3,MnO2 and Th(NO3)4·4H2O, were mixed uniformly using a traditional ball milling, which resulted in a uniform particle size distribution in the mixed powers. Tests of X-ray diffraction, SEM, impedance spectra and charge-discharge were carried out for LiThxMn1-xO4 cathode materials. Results show that the synthesized LiTh0.01Mn1.99O4 material exhibits standard spinel structure, regular particle morphology and excellent property of charge-discharge for big current. The capacity retention of the material modified by doping Th is more than 85.1% of the first discharge specific capacity of 111.5 mAh·g -1 after 20 cycles at the current rate 1C, while the pristine LiMN2O4 is only 57% of the first discharge specific capacity of 110.2 mAh·g-1 after the same cycles at the same current rate.     

甲型肝炎病毒(L-A-1株)基因型分析

目的 分析甲肝病毒基因型,为确定我国甲肝的分子流行病学及疫苗的安全性和免疫原性奠定基础。方法 采用抗原捕获聚合酶链反应（AC/PCR）,依据国际上甲肝病毒分型标准,扩增VP1/2A结合处的168个核苦酸（nt2909～3264）。结果 经生物信息学软件分析,得出L-A-1株病毒属于甲肝病毒基因IB亚型。结论 在我国有IA和IB两个亚型甲肝病毒流行。     

双电层电容器用沥青焦基活性炭的制备工艺条件对其孔结构及电化学性能的影响

以沥青焦为原料，KOH为活化剂在不同的工艺条件下制备了双层电容器用活性炭电极材料。分别考察了活化剂用量、活化时间、以及加入Cu、Ni催化活化等工艺条件对活性炭孔结构及作为双电层电容器电极的电化学性能的影响。结果表明：在实验范围内增加KOH用量及活化时间，活性炭的比表面积和比电容增加，比电容最高达到247F／g。添加Cu、Ni催化活化后活性炭的比表面积及比电容增加，高功率放电性能明显改善。     

交流接触器温度场仿真及试验验证

将ANSYS有限元热分析应用到交流接触器热特性分析中,模仿其实际工作环境,构建交流接触器三维稳态热分析模型,确定热源、导热系数和表面散热系数,对接触器的稳态温度场进行分析;进一步改变施加的边界条件,研究不同散热方式下接触器的温度分布。最后对CJX2-0910型交流接触器进行温升试验,将温度场的仿真结果与试验结果比较,误差较小,表明所建立热分析模型的可行性。研究结果对接触器材料的选择、结构的设计及其性能的优化有重要意义。     

Reaction Coupling of Ethylbenzene Dehydrogenation with Nitrobenzene Hydrogenation

The chemical equilibrium for the coupling of ethylbenzene dehydrogenation with nitrobenzene hydrogenation, to produce styrene and aniline simultaneously, has been calculated on the basis of the Soave–Redlich–Kwong equation of state. The dehydrogenation of ethylbenzene in the presence of nitrobenzene over the catalysts -Al₂O₃, ZSM-5, activated carbon and platinum supported on activated carbon has been carried out at 400 °C. The effects of Pt loading and the pretreatment of the catalysts have been investigated. It has been revealed that the conversion of ethylbenzene can be greatly improved by the reaction coupling due to the elimination of the hydrogen produced in the reaction by the hydrogenation of nitrobenzene. Platinum supported on the activated carbon has been suggested as a suitable catalyst. The best results with ethylbenzene conversion of 33.8% and styrene selectivity of 99.2% were obtained over Pt(0.02 wt%)/AC at 400 °C. Moreover, such process is also energetically favored since the necessary process heat to drive the ethylbenzene dehydrogenation can be provided by the coupling with the exothermic nitrobenzene hydrogenation reaction.     

A study of PtRuO2 catalysts thermally formed on titanium mesh for methanol oxidation

Platinum-based catalysts, for the electro-oxidation of methanol, have been made by thermal decomposition of chloride precursors onto titanium mesh. The catalysed electrodes were successfully operated in acidic methanol electrolytes. Electrochemical characterisation has been carried out using cyclic voltammetry, electrochemical impedance spectroscopy and galvanostatic polarisations. A complete analysis of the electrochemical results showed that the preliminary performance of the catalysed titanium mesh was comparable to that achieved with carbon-supported PtRu catalysts. The catalysts formed on titanium mesh by thermal decomposition also exhibited dimensional stability. Catalysed titanium mesh therefore appears to be a promising alternative to carbon-supported catalysts for certain fuel cell applications.