任丘油田雾迷山油藏抽油机井系统效率初步探讨

总公司1996年对任丘雾迷山油藏抽油机井进行测试,系统效率高达51%~68%,其结果出乎意料。从影响抽油机系统效率的几大因素入手,分析出任丘雾迷山油藏抽油机井系统效率高的主要原因。任丘雾迷山油藏属裂缝性破酸盐岩油藏(即灰岩油战),由于其裂缝发育、渗透性好、油层厚度大、地层温度高、油气比小、饱和压力低等,使得抽油机井生产呈现如下特点:()大泵径,长冲程,低冲次大排量采油;(2)中浅京挂,小沉没度;(3)抽汲流体为液体单相,泵充满程度高;(4)部分井为连抽"带喷"状态,抽油系活塞底部受力大;(5)井液粘度低,油井不结蜡,摩阻损失小。由于这些特点以及近年来使用的新型节能抽油机,使得抽油机井系统效率大大高于其它油田抽油机井系统效率。     

INMARSAT 21世纪工程——全球个人移动卫星通信

本文概述INMARSAT 21世纪工程的规划及为实现这一规划,INMARSAT组织在本世纪末正在进行和即将进行的一系列卫星通信技术工作。着重阐述INMARSAT 21世纪工程的业务性能以及对三种卫星布局方案进行抉择的新动向。     

G~2－连续的保凸插值三次Bezier样条曲线

本文引入曲率参数，描述了分段三次Ｂｅｚｉｅｒ插值样条曲线（开的和闭的）。这些插值曲线是Ｇ~２－连续的和保凸的，并且这些曲线可以作局部修改。最后，用本文的方法解决了一个实际问题。     

利用地理信息系统ARC/INFO计算地物面积的方法

详细介绍利用地理信息系统工具ARC/lNFO来计算地物分布专题图中各种不同地物面积的方法，并给出海南省大边河库区地物面积的计算实例。     

基于工作站和EUCLID－IS的计算机组装结构CAD系统研究

随着集成电路技术的发展及计算机性能的不断提高，计算机组装结构设计在计算机，总体设计中的地位越来越重要，它直接影响到计算机性能的提高。本文针对一个基于工作站和ＥＵＣＬＩＤ－ＩＳ软件的电子计算机组结构ＣＡＤ系统，从软、硬件平台，系统功能及实现等方面进行了讨论，旨在为电子计算机组装结构设计提供一种强有力的、方便的设计工具，有利于增强国产计算机的市场竞争能力。     

VME总线评述

ＶＭＥ总线是应用最广泛的国际总线标准之一。本文介绍了ＶＭＥ总线的结构特别，包括信号名的定义及功能等，特别阐明了ＶＭＥ总线的并行性、实时性和高可靠性，突出了ＶＭＥ总线的发展前景。     

基于图形约束的工程图纸扫描图象表面粗糙度的自动识别

本文通过分析现有工程图纸扫描图象的识别与理解系统，提出了表面粗造度的自动识别算法，从而弥补了以往系统的不足，基于图形约束的表面粗造度整体识别算法符合技术人员的读图规律，处理速度快，可靠性高，该算法已在微机上调试成功。     

Poly(3-octylthiophene) as semiconductor for schottky barrier: Effects of doping and storage time

Schottky diodes of aluminium/poly(3-octylthiophene)(P30T)/indium-tin oxide with large active area are prepared by using the proposed new casting technique. Their rectifying behavior and junction characteristics are dependent on whether the P30T is doped and on the storage time, but independent of the thickness of the P30T layer. The present technique can also be applied in a fabrication of electronic devices with other soluble conjugated polymers.     

Kinetic analysis of the coding properties of O6-methylguanine in DNA: the crucial role of the conformation of the phosphodiester bond

Production by N-nitroso compounds of O6-alkylguanine (O6-alkylG) in DNA directs the misincorporation of thymine during DNA replication, leading to G:C to A:T transition mutations, despite the fact that DNA containing O6-alkylG:T base pairs is less stable than that containing O6-alkylG:C pairs. We have examined the kinetics of incorporation by Klenow fragment (KF) of Escherichia coli DNA polymerase I of thymine (T) and of cytosine (C) opposite O6-MeG in the template DNA strand. Both T and C were incorporated opposite O6-MeG much slower than nucleotides forming regular A:T or G:C base pairs. Using various concentrations of dTTP, dCTP, or their phosphorothioate (Sp)-dNTP alpha S analogues, or a mixture of dTTP and dCTP, the progress of incorporation of a single nucleotide in a single catalytic cycle of a preformed KF-DNA complex was measured (pre-steady-state kinetics). The results were consistent with the kinetic scheme (Kuchta, R. D., Benkovic, P., & Benkovic, S. J. (1988) Biochemistry 27, 6716-6725): (1) binding of dNTP to polymerase-DNA; (2) conformational change in polymerase; (3) formation of phosphodiester between the dNTP and the 3'-OH of the primer; (4) conformational change of polymerase; (5) release of pyrophosphate. The results were analyzed mathematically to identify the steps at which the rate constants differ significantly between the incorporation of T and C. The only significant difference was the 5-fold difference in the rates of formation of the phosphodiester bond (for dTTP, kforward = 3.9 s-1 and kback = 1.9 s-1; for dCTP, kforward = 0.7 s-1 and kback = 0.9 s-1). These pre-steady-state progress curves were biphasic with a rapid initial burst followed by an apparently steady-state rise. Deconvolution of these curves gave direct evidence for the importance of the conformational change after polymerization by showing that the curves represented the sum of the rapid accumulation of the product of step 3 followed by the slow conversion of that to the product of step 5 (because of the rapidity of the release of pyrophosphate there was no significant accumulation of the product of step 4). The equilibrium constants for each step suggest that the greatest change in the Gibbs free energy occurs at the conformational change after polymerization and that while the formation of the phosphodiester bond to T is slightly exothermic, that to C is slightly endothermic.(ABSTRACT TRUNCATED AT 400 WORDS)