节能气动系统数学模型的改进

作者曾提出一种节能近50%的节能气动系统,进行了理论与实验研究。本文重新定义特征时间 T_m~″和有效面积比 a_(?)~″,改进了它的退回阶段Ⅲ的动特性数学模型,使之能更准确地描述系统的真实特性,仿真结果与实验结果更趋一致。     

工矿企业能量平衡通用模式的研究

提出了适用于工矿企业能量平衡的一种通用模式，将与ＧＢ３４８４－８３《企业能量平衡通则》再增加“一表两图”──“企业能量平衡表”、“企业能源网络图”和“企业能流图”的效果相一致，能更加科学、合理地反映企业能量平衡的结果。     

田径运动的现状分析与发展对策--曲靖师范学院参加云南省第四届大运会后的思考

通过对曲靖师范学院田径队参加云南省第四届大学生运动会比赛成绩的综合分析，说明曲靖师范学院田径运动教学与训练中存在的问题，并对存在问题提出合理项目布局、运动队训练、教练员队伍、体育科研方面等的对策．     

重庆主城区社区体育的现状调查

采用问卷调查、文献资料、数理统计等研究方法，对重庆市主城区社区体育现状进行调查，分析了社区居民参加体育活动的内容、时间、地点、形式、规模，以及社区体育的服务管理、设施管理、体育人才管理、体育经营管理系统，并提出了符合实情，可体现地理、环境特点的重庆主城区社区体育发展对策。     

关于玉林师院学生参加课外体育活动的调查研究

采用问卷调查与数理统计相结合的方法，对玉林师院学生参加课外体育活动的情况进行调查研究。结果显示，大部份的学生喜欢参加课外体育活动，动机是好的，时间为每周2小时左右居多。另外，调查中反映，学校场地不足、器材少是影响学生参加课外体育活动主要的因素。     

NSRL-XAFS光束线弧矢聚焦双晶单色器设计

针对XAFS光束线能量动态扫描的实验特点，介绍了弧矢聚焦双晶单色器的物理设计：包括晶体光学结构、性能参数计算、晶体热载分析和弧矢弯曲原理．弧矢缩比选择为1：4．88，水平接收角由原来的1mrad拓宽到3mrad，在不改变基本配置的情况下，获得了样品上束癍缩小、光子通量高达半个量级以上的增益．     

YN相互作用和轻超核∧^5He结合能的计算

在手征SU(3)夸克模型基础上，用共振群方法，给出∧N相互作用的非定域位，并用于轻超核∧^5He的结合能的计算，得到了与实验和其他方法相近的结果．     

配电变压器经济运行方式研究

通过分析变压器损耗，采用某110kV变电站两台主变进行验证，提出一种新的配电变压器经济运行算法，使变压器达到降低损耗．节约能源和经济运行的目的。     

Fluoro-Compounds in Electrolytes for Energy Storage Devices

1 Results Electrochemical energy storage devices such as lithium-ion batteries[1-2] and double-layer capacitors[3-4] have attracted a great deal of attention because of their potential application to electric hybrid vehicles. They utilize nonaqueous electrolyte solutions comprising from organic solvents and lithium or quaternary ammonium salts with fluorine-containing anions. This is because the relatively large anions with electron-withdrawing atoms enable ionic dissociation in dipolar aprotic solvents...     

Deactivation reactions in the modeled 2,2,6,6‐tetramethyl‐1‐piperidinyloxy‐mediated free‐radical polymerization of styrene: A comparative study with the 2,2,6,6‐tetramethyl‐1‐piperidinyloxy/acrylonitrile system

The competitiveness of the combination and disproportionation reactions between a 1‐phenylpropyl radical, standing for a growing polystyryl macroradical, and a 2,2,6,6‐tetramethyl‐1‐piperidinyloxy (TEMPO) radical in the nitroxide‐mediated free‐radical polymerization of styrene was quantitatively evaluated by the study of the transition geometry and the potential energy profiles for the competing reactions with the use of quantum‐mechanical calculations at the density functional theory (DFT) UB3‐LYP/6‐311+G(3df, 2p)//(unrestricted) Austin Model 1 level of theory. The search for transition geometries resulted in six and two transition structures for the radical combination and disproportionation reactions, respectively. The former transition structures, mainly differing in the out‐of‐plane angle of the N? O bond in the transition structure TEMPO molecule, were correlated with the activation energy, which was determined to be in the range of 8.4–19.4 kcal mol^?1 from a single‐point calculation at the DFT UB3‐LYP/6‐311+G(3df, 2p)//unrestricted Austin Model 1 level. The calculated activation energy for the disproportionation reaction was less favorable by a value of more than 30 kcal mol^?1 in comparison with that for the combination reaction. The approximate barrier difference for the TEMPO addition and disproportionation reaction was slightly smaller for the styrene polymerization system than for the acrylonitrile polymerization system, thus indicating that a β‐proton abstraction through a TEMPO radical from the polymer backbone could diminish control over the radical polymerization of styrene with the nitroxide even more than in the latter system. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 232–241, 2007