关于世行贷款基础教育项目实施效果的调查

世界银行贷款第四个贫困地区基础教育发展项目 ,自 1997年在我国西部贫困地区启动以来 ,取得了实实在在的成效。本文以云南省宣威市“贫四项目”实施效果为对象 ,进行了实事求是的调查与分析     

4G移动通信系统及其关键技术

提出了3G通信系统的局限性,概述了4G通信系统的特点和关键技术,对4G系统网络结构作了简单介绍。     

Monte Carlo散射标记方法在辐射防护设计中的应用

在X射线检查系统中,辐射防护中除了需要重点考虑透射和漏射外,散射的成分也必须考虑,而且散射的影响变得越来越重要,这一点在同方威视的固定式、组合式和车载式系统中都已经得到了体现。针对散射的问题,该文进行了系统的研究,提出了在Monte Carlo计算中采用散射标记方法分析各散射体对于散射的贡献,克服了传统方法无法准确计算某一点的散射剂量率以及各散射体对散射的贡献的局限,并利用实验进行了验证。该文采用的计算工具是Geant4软件包。结果表明,该文提出的方法是可行的,尤其在复杂系统的辐射防护优化设计中具有较好的指导作用。     

The Development of Materials for the Production of Hydrogen from Bio-ethanol

1 Results There is an increased interest in the hydrogen production from renewable sources. In this context, recently, numerous studies which use ethanol for hydrogen production have appeared. Ethanol is easily handled, non-toxic, and it can be obtained from biomass. The steam-reforming of bioethanol has been shown to beeffective for hydrogen production:C2H5OH 3 H2O  6 H2 2 CO2. Six moles of hydrogen can be yielded for each mole of ethanol reacted. However, depending on the catalyst used, other und...     

基于SQL的报表生成系统

本文介绍的报表生成系统的取数方式可用ＳＱＬ语句，使系统具有通用性，灵活性等特点。在系统实现中采用了多窗口全屏幕方式定义报表格式及取数方式。系统用户界面友好，直观、简单易学。     

Minkowski时空中的四维力

Ｍｉｎｋｏｗｓｋｉ时空中的四维力刘泽文（物理系）关键词：相对论／类时；类空；类光；四维力分类号：Ｏ４１２在Ｍｉｎｋｏｗｓｋｉ时空中，诸如四维电流密度Ｊ￣μ、粒子的四维加速度ω￣μ＝ｄＵ￣μ／ｄτ以及四维波矢Ｋ￣μ等向量，其类时、类空以及类光性质一般是...     

新型固体酸SO_4~(2-)MoO_3-TiO_2催化合成苹果酯

自制了一种新固体酸催化剂SO2 -4MoO3 -TiO2 ,FT -IR谱图表明 ,催化剂表面具有强酸中心 ,该催化剂对苹果酯合成的活性高 ,并得到该反应的优化条件如下 :乙酰乙酸乙酯 0 .3mol,乙二醇 0 .6mol,环己烷 30ml,催化剂 3g ,反应温度 110℃ ,反应时间 1.5h ,在此条件下 ,苹果酯产率达 90 % ,且催化剂易回收 ,具有较好的重复使用性能     

Ab initio study of the effects of Ag/Mn doping on the electronic structure of LiFePO_4

Based on density functional theory (DFT) of the first-principle for the cathode materials of lithium ion battery, the electronic structures of Li(Fe1-xMex)PO4 (Me = Ag/Mn, x = 0―0.40) are calculated by plane wave pseudo-potential method using Cambridge serial total energy package (CASTEP) program. The calculated results show that the Fermi level of mixed atoms Fe1-xAgx moves into its conduction bands (CBs) due to the Ag doping. The Li(Fe1-xAgx)PO4 system displays the periodic direct semiconductor characteristic with the increase of Ag-doped concentration. However, for Fe1-xMnx mixed atoms, the Fermi level is pined at the bottom of conduction bands (CBs), which is ascribed to the interaction be-tween Mn(3d) electrons and Fe(4s) electrons. The intensity of the partial density of states (PDOS) near the bottom of CBs becomes stronger with the increase of Mn-doped concentration. The Fermi energy of the Li(Fe1-xMnx)PO4 reaches maximum at x = 0.25, which is consistent with the experimental value of x = 0.20. The whole conduction property of Mn-doped LiFePO4 is superior to that of Ag-doped LiFePO4 cathode material, but the structural stability is reverse.     

Theoretical study on the lithium bond interaction of furan homologues C_4H_4Y (Y=O, S) with LiCH_3 via DFT and MP2

The optimizations geometries and interaction energy corrected by BSSE of the complexes between C4H4Y (Y=O, S) and CH3Li have been calculated at the B3LYP/6-311 G** and MP2/6-311 G** levels. Three complexes were obtained. Abnormally, the calculations showed that all the C10—Li14 bond lengths increased obviously but the blue-shift of C10—Li14 stretching frequency occurred after formed complexes. The calculated binding energy with basis set super-position error (BSSE) and zero-point vibrational energy corrections of complexes I―III is ?45.757, ?35.700 and ?39.107 kJ·mol?1, respectively. The analyses on the combining interaction with the atom-in-molecules theory (AIM) also showed that a relatively strong lithium bond interaction presented in furan homologues C4H4Y---LiCH3 systems. Natural bond orbital theory (NBO) analysis has been performed, and the results revealed that the com- plex I is formed with n-σ type lithium bond interaction between C4H4O and LiCH3, complex II is formed with π-s type lithium bond interaction between C4H4O and LiCH3, and complex III is formed with π-s and n-s type lithium bond interactions between C4H4S and LiCH3, respectively.