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151.
利用谱分解技术进行薄储层预测 总被引:35,自引:0,他引:35
采用短时窗离散傅里叶变换的频谱分解技术,实现了在频率域内通过调谐振幅的成像特征来研究储层横向变化规律的目标,最大限度地挖掘了地震资料主频至高频端的地震分辨能力。本文介绍了谱分解技术的基本原理、谱分解数据体的类型及其解释方法,充分利用谱分解得到的一系列单一频率的调谐振幅数据体研究辽河盆地东部凹陷西斜坡铁匠炉地区近源沉积砂砾岩储层,查清了该套储层沉积相带的平面分布和有效储层横向展布特征,预测结果已被钻井所证实。 相似文献
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In this paper mud was treated as the Bingham fluid. In staggered grids, two-dimensional incompressible Navier-Stokes equations for non-Newtonian fluid was solved by the MAC method. Numerical simulations were conducted on mud bed-generating phenomenon and mud impacting a wall along a slope. The distributions of free surface, pressure and velocity of mud and water were obtained. The results indicate that the computed layer thickness of mud bed almost equals the theoretically predicted value. Because of the differences in constitutive relationship, the distributions of free surface are different for water and mud. The distortion of water free surface is much more complicated. 相似文献
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157.
本文报道采用液相外延(LPE)生长和传统光刻制管工艺研制出引入多层(三层或三层以上)中间能带隙过渡的吸收区、倍增区分离的InGaAs(P)/InP雪崩光电二极管(简称InGaAs(P)/InPSAGMAPD),其技术指标为:击穿电压VB=40~90V;0.9VB时的暗电流Id最小可小于10nA;1.3μm时光响应度Re=0.6~0.8A/W,倍增因子M≥20(Mmax>40),过剩噪声因子F≌5和较宽频带响应特性。 相似文献
158.
对院基寺水库运行过程中出现的坝基渗漏现象进行了全面的描述,结合坝址工程地质和水文地质条件、施工情况及坝体结构,系统地分析了产生渗漏的原因及渗漏途径,并提出了防渗帷幕灌浆处理方案。灌浆试验、现场施工质量检查及实际观测成果证实,工程处理措施取得了良好的效果。 相似文献
159.
Xu Baowen Zhang Weifeng 《电子科学学刊(英文版)》2002,19(4)
The users' interest can be mined from the web cache and can be used widely. The interest can be specialized by the two-tuple (term, weight) in the simple interest model, in which the association relations are not mined, and then the interest cannot be associated in expressing the users' interest. Based on analyzing the WWW cache model, this letter brings forward a two-dimensional interest model and gives the interrelated methods on how to store the two-dimensional interest model effectively. 相似文献
160.
The kinetics of substrate removal by the liver and the resulting nonlinear changes in unbound fraction along the flow path at varying input drug concentrations were examined by a model simulation study. Specifically, we varied the binding association constant, KA, and the Michaelis-Menten constants (Km and Vmax) to examine the steady state drug removal (expressed as hepatic extraction ratio E) and changes in drug binding for (i) unienzyme systems and (ii) simple, parallel metabolic pathways; zonal metabolic heterogeneity was also added as a variable. At low KA, E declined with increasing input drug concentration, due primarily to saturation of enzymes; only small differences in binding were present across the liver. At high KA, a parabolic profile for E with concentration was observed; changes in unbound fraction between the inlet and the outlet of the liver followed in parallel fashion. Protein binding was the rate-determining step at low input drug concentrations, whereas enzyme saturation was the rate-controlling factor at high input drug concentration. Heterogeneous enzymic distribution modulated changes in unbound fraction within the liver and at the outlet. Despite marked changes in unbound fraction occurring within the liver for different enzymic distributions, the overall transhepatic differences were relatively small. We then investigated the logarithmic average unbound concentration and the length averaged concentration as estimates of substrate concentration in liver in the presence of nonlinear drug binding. Fitting of simulated data, with and without assigned random error (10%), to the Michaelis-Menten equation was performed; fitting was repeated for simulated data obtained with presence of a specific inhibitor of the high-affinity, anteriorly distributed pathway. Results were similar for both concentration terms: accurate estimates were obtained for anterior, high affinity pathways; an overestimation of parameters was observed for the lower affinity posteriorly distributed pathways. Improved estimations were found for posteriorly distributed pathways upon inhibition with specific inhibitors; with added random error, however, the improvement was much decreased. We applied the method for fitting of several sets of metabolic data obtained from rat liver perfusion studies performed with salicylamide (SAM) (i) without and (ii) with the presence of 2,6-dichloro-4-nitrophenol (DCNP), a SAM sulfation inhibitor. The fitted results showed that SAM sulfation was a high-affinity high-capacity pathway; SAM glucuronidation was of lower affinity but comparable capacity as the sulfation pathway, whereas SAM hydroxylation was of lower affinity and lower capacity. 相似文献