基于DVB/MPEG-2的卫星Internet技术

Internet的快速发展，使他已陷入了自身难以克服的困境，这种困境主要来自于骨干网、接入网、服务器三种瓶颈。而卫星通信与Internet的结合能有效地解决目前的这种困境。本文介绍了基于DVB／MPEG-2的卫星Internet原理、结构、应用及其关键技术，并引入了2种现有成熟的Internet接入技术：VSAT接入方式和VSAT与CATV结合接入方式。     

有线电视中数字电视前端设计

随着有线电视中数字电视逐步取代模拟电视，有线电视数字电视前端的设计愈显重要。分析有线电视中数字电视前端的组成和设备功能，以一个频点为例介绍如何进行数字电视前端的设计。     

发射极δ掺杂的InGaAs/InPDHBT的特性分析

设计了一种新结构的InGaAs/InP双异质结晶体管(DHBT),其中发射结采用δ掺杂和阻挡层结构,集电极采用N+掺杂复合结结构.考虑隧穿作用和发射结空间电荷区复合电流的影响,计算了δ掺杂浓度和N+、n-层厚度等参数变化对InGaAs/InP DHBT电流、I-V输出特性、电流增益的影响,计算结果表明,随着这些参数值增大,InGaAs/InP DHBT输出特性逐渐改善.当δ掺杂浓度大于2×1012cm-3时,电流增益趋于饱和.     

底部框剪砌体房屋空间弹塑性地震反应分析

本文提出了底部框剪砌体房屋这类上下混合承重结构体系的空间弹塑性地震反应时程分析方法。针对砌体结构和框架抗震墙结构截然不同的抗震性能，对上部砌体结构采用空间剪扭分析法，而对下部框架抗震墙结构采用空间协同分析法，建立了组合型串联刚片系振动模型。对单向和双向地震波输入结构层位移反应进行了比较。     

5-(4''-甲基联苯-2-基)-1H-四唑的合成研究进展

5-(4-甲基联苯-2-基)-1H-四唑是血管紧张素Ⅱ受体拮抗剂的关键原料,综述其合成方法的研究进展.     

Photocatalytic degradation of 2,2‐bis(4‐hydroxy‐3‐methylphenyl) propane (BPP) based on molecular recognition interaction

BACKGROUND: Endocrine disruptors in the aquatic environment and their potential adverse effects are currently issues of concern. One of these endocrine disruptors is 2,2‐bis(4‐hydroxy‐3‐methylphenyl)propane (BPP). In this work the molecular recognition interaction of BPP with β‐cyclodextrin (β‐CD) was studied using IR spectroscopy and steady state fluorescence spectroscopy, and the photocatalytic degradation behaviour of BPP based on molecular recognition interaction was investigated in a TiO₂/UV–visible (λ_max = 365 nm) system. This might provide a new method for the treatment of some organic pollutants in wastewater. RESULTS: β‐CD reacts with BPP to form a 1:1 inclusion complex, the formation constant of which is 4.94 × 10³ L mol^?1. The photodegradation rate constant of BPP after molecular recognition by β‐CD showed a 1.42‐fold increase in the TiO₂/UV–visible (λ_max = 365 nm) system. The photodegradation of BPP depended on the concentration of β‐CD, the pH value, the gaseous medium and the initial concentration of BPP. The photodegradation efficiency of BPP with molecular recognition was higher than that without molecular recognition. After 100 min of irradiation the mineralisation efficiency of BPP after molecular recognition by β‐CD reached 94.8%, whereas the mineralisation efficiency of BPP before molecular recognition by β‐CD was only 40.6%. CONCLUSION: The photocatalytic degradation of BPP after molecular recognition by β‐CD can be enhanced in the TiO₂/UV‐visible (λ_max = 365 nm) system. This enhancement is dependent on the enhancement of the adsorption of BPP, the moderate inclusion depth of BPP in the β‐CD cavity and the increase in the frontier electron density of BPP after molecular recognition. Copyright © 2008 Society of Chemical Industry     

Material removal and surface damage in EDM of Ti3SiC2 ceramic

Material removal and surface damage of Ti₃SiC₂ ceramic during electrical discharge machining (EDM) were investigated. Melting and decomposition were found to be the main material removal mechanisms during the machining process. Material removal rate was enhanced acceleratively with increasing discharge current, i_e, working voltage, u_i, but increased deceleratively with pulse duration, t_e. Microcracks in the surface and loose grains in the subsurface resulted from thermal shock were confirmed, and the surface damage in Ti₃SiC₂ ceramic led to a degradation of both strength and reliability.     

纳秒级上升时间的高压脉冲群电源

按照IEC 61000-4-4/GB 17626.4—1998的要求，首先应用PSPICE仿真确定电路中各元件的参数值，然后基于拉普拉斯变换用MATLAB求解二阶电路验证各元件参数。在此基础上研制了一台以开关电源作为高压直流电源、以氢闸流管作为主控开关的脉冲群电源。该电源体积小、重量轻、效率高、成本低廉。试验结果表明，其输出信号符合标准要求，可用于快速瞬变脉冲群抗扰度试验。     

昆2井优快钻井及油气层保护技术

昆2井是一口位于柴北缘西段的昆特依凹陷潜伏Ⅰ号圈闭上的风险探井,设计井深为5950m。针对柴北缘深探井存在的主要技术难题,制定了昆2井的技术对策。通过对钻井设备的优选、井身结构的优化、钻头及钻具组合的优选、钻井参数及钻井液性能的优化、油气层保护技术的研究与应用,形成了一套适合于柴北缘的优快钻井技术,使昆2井的完钻井深达到5950m。与邻区的深探井平均水平相比,在井深增加888m、大尺寸井眼段更长的前提下,昆2井的钻井、完井周期分别缩短了98.75d、124.2d,钻机月速度增加了317m/台,平均机械钻速增加了0.82m/h。根据“理想充填新理论”,确定了保护油气层的最优复配暂堵方案,利用该方案所配制的钻井液其渗透率恢复值达到了87.5%以上,流变性能良好,滤失量低,对改善泥饼质量、增强井壁稳定性有明显的效果。     

Cis–trans isomerization of olefinic alcohols promoted by Rh(I) complexes

Homogeneous hydrogenation and isomerization reaction of cis-2-butene-1,4-diol has been investigated in ethanol by using tris(triphenylphosphine)chlororhodium(I), RhCl(PPh₃)₃, and triethylamine at 303 K and 0.01–0.1 MPa partial hydrogen pressure. Under reduced H₂ pressure, the geometric isomerization reaction occurs, to a high extent, leading to trans-2-butene-1,4-diol up to 93% selectivity at 90% conversion of the cis analogous. Effects of H₂ partial pressure as well as triethylamine, added phosphine and olefin concentrations on the rate of reaction and on the products distribution were also investigated. The results obtained can be interpreted on the basis of a proposed mechanism in which RhH(PPh₃)₃ is the active species. The high selectivity towards cis-trans isomerization of cis-2-butene-1,4-diol is attributed to steric factors of the Rh(I) coordinated triphenylphosphine groups.