共查询到18条相似文献，搜索用时 109 毫秒
1.
油水饱和泥质砂岩中流动电位的研究对于揭示含油储层震电勘探和动电测井的机理有着重要的意义.本文首先从岩石孔隙的微观结构出发,构造了描述水润湿条件下油水饱和泥质砂岩储层的毛管模型.在模型中依据油水流动遵守的Navier-Stokes方程和电化学传质动力学理论,建立了描述油水饱和泥质砂岩流动电位的数学方程,并数学模拟了岩石储渗参数对流动电位频散特性的影响规律.研究结果表明:储层孔隙内流体受到的粘滞力与惯性力控制着水相和油相的流动,从而决定了流动电位的频散特性.随着孔隙度的增大,油水两相各自的有效渗透率均增大;而含水饱和度的升高使得水相有效渗透率增大,油相有效渗透率减小.在水润湿条件下,流动电位耦合系数随含水饱和度升高而增大,随束缚水饱和度的升高而减小.另外,流动电位相对耦合系数也随含水饱和度的升高而增大,但无频散现象. 相似文献
2.
利用储层岩石流动电位的频散特性评价复杂储层已经成为勘探地球物理领域关注的热点,但是目前还没有形成基于储层岩石储渗特性及电化学性质的具有普遍指导意义的理论方法和数学模型.本文利用微观毛管理论,通过随时间谐变条件下渗流场和电流场的耦合模型,建立了描述储层岩石流动电位频散特性的数学方法,定量分析了频率域储层岩石动态渗透率、动电耦合系数和流动电位耦合系数随储层岩石孔隙度、溶液浓度和阳离子交换量的变化规律.研究结果表明:储层岩石流动电位频散特性是储层流体惯性力与流体黏滞力相互作用的结果.储层岩石孔隙度越大,储层维持流体原有运动状态的能力越大,临界频率越小;储层岩石的溶液浓度和阳离子交换量对临界频率没有影响.储层岩石的孔隙度越大,流体流动能力越强,流动电位各耦合系数的数值越大;溶液浓度越小或阳离子交换量越大,孔隙固液界面的双电层作用越强,各耦合系数的数值越大. 相似文献
3.
4.
本文对利用自然电位法探测岩溶地下河做了探索性研究.选择桂林市寨底地下河发育良好的区域,通过阵列式连续时间观测方式获得了随时间连续变化的自然电位数据.提出自然电位数据阻尼最小二乘多参数逐步解析反演方法,并对获得的数据进行反演,以此提取数据中极化源的信息,包括极化源位置、极化角度和极化强度等.在所有时间道的数据反演结果中,将观测范围内极化源的空间位置等参数绘制成相应图件,与观测区地下河资料进行对比研究.研究结果表明:该反演方法能够有效提取自然电位数据中隐含的极化源信息;极化源位置可作为判断含水构造空间位置的依据,极化角度和极化强度可用来区别含水构造类型;多参数综合解释可有效定位地下河的平面位置. 相似文献
5.
实验室研究发现不含金属矿物的饱和多孔介质激发极化参数受岩石物理特性影响,建立岩心尺度的低频(<106 Hz)复电导率与孔隙结构参数、流体属性等因素之间的定量关系对解释激发极化数据具有重要指导意义.然而,产生激发极化效应的原因还未形成统一的物理/化学过程认识,现有理论未能完全解释激发极化数据,激电参数与多孔介质结构参数之间的定量关系缺少深入的机理研究.为此,本文首先阐述了双电层理论和用以解释激发极化效应的机理,包括Stern层极化、膜极化、Maxwell-Wagner极化和动电效应等;其次,总结了现有激发极化模型研究的最新进展,包括等效电路模型、Stern层极化模型、膜极化模型、等效介质模型等.综述表明：(1)低频激发极化效应的微观机理仍未达成统一认知,在特定条件下,膜极化模型与Stern层极化模型都能解释低频激发极化数据;(2)特征弛豫时间受孔径或粒径控制仍存在争议. 相似文献
6.
在水介质中顺序添加分散粘土颗粒、油珠、导电骨架颗粒、层状泥质,并对每一种成分进行连续积分,建立了一种适用骨架导电及含有分散粘土和层状泥质的泥质砂岩通用电阻率模型.通过对该模型的影响因素分析,发现泥质分布形式对模型计算的含水饱和度有很大影响;对应两个不同粘土颗粒电阻率或骨架颗粒电阻率的地层电导率之差,几乎与总含水饱和度无关,而对应两个不同层状泥质电阻率的地层电导率之差,随总含水饱和度增大而增大;骨架胶结指数变化对地层电导率与总含水饱和度关系曲线的影响最大,而粘土胶结指数变化对地层电导率与总含水饱和度关系曲线的影响最小;饱和度指数对地层电导率与总含水饱和度关系曲线的影响随总含水饱和度的增大而减小.通过一组骨架导电的人造岩样的试验,表明当地层水电阻率.小于颗粒电阻率时,该模型可以用于不含粘土的骨架导电的岩石.通过两组分散泥质砂岩岩样实验测量数据和一组层状泥质砂岩测井资料及实际测井资料的计算,表明本文给出的电阻率模型既适用于分散泥质砂岩地层解释又适用于层状泥质砂岩地层解释,同时,还适用于含有分散粘土和层状泥质的混合泥质砂岩地层解释. 相似文献
7.
《地球物理学进展》2016,(4)
A地区致密砂岩储层具有孔隙结构复杂、高泥、高钙的特征,使其导电规律更复杂,现用饱和度模型不能全面描述三种因素对致密砂岩导电规律的影响,造成A地区致密砂岩储层饱和度评价精度较低.本文首先从实验角度分析了孔隙结构、泥质、钙质胶结对致密砂岩导电规律的影响,得出随孔隙结构变差、泥质含量减小、钙质含量增加,岩石导电性变差.其次,考虑影响A区致密砂岩导电规律三种主要因素,利用有效介质对称导电理论具有描述泥质和钙质胶结对岩石导电性影响的优点,而改进等效岩石元素理论具有更好的描述孔隙结构变化对岩石导电性影响的优点,将两种理论结合,建立了适用于致密砂岩储层饱和度评价的导电模型.理论分析表明,建立的致密砂岩导电模型能正确地描述孔隙结构、泥质、钙质胶结对致密砂岩导电规律的影响,并与实验规律相符.第三,基于含水致密砂岩可动流体孔隙中水流与电流流动的相似性以及改进等效岩石元素模型和弯曲毛管模型,建立了有效流动孔隙度计算式.利用半径均值和无效流动孔隙与有效流动孔隙之比对致密砂岩孔隙结构进行了分类,在分类基础上,采用优化技术和有效流动孔隙度计算式,建立了孔隙结构效率和孔隙曲折度计算式.利用致密砂岩岩电实验数据,采用优化技术确定了模型中流体非均匀分布指数、渗滤速率及渗滤指数等参数值,并建立了相应参数计算式.与密闭取心井的饱和度对比,致密砂岩导电模型计算的含水饱和度平均绝对误差为4.5%;与试油结果对比,解释结果与试油结论吻合.这表明所建立的导电模型适用于A地区含泥含钙致密砂岩储层饱和度评价. 相似文献
8.
《地球物理学进展》2016,(4)
复杂泥质砂岩储层的饱和度评价一直是测井解释领域亟待解决的难点和热点问题,基于并联导电理论和阿尔奇公式建立的导电模型扩展性有限,在一定程度上限制了该类模型扩展描述孔隙结构更复杂的高泥高钙砂岩储层的导电规律,而有效介质对称导电理论能很好地描述复杂泥质砂岩储层导电规律,具有很好的应用前景,但仍需深入研究.首先针对纯砂岩,使用有效介质对称导电理论建立纯砂岩有效介质对称导电模型,理论分析与实验研究表明纯砂岩有效介质对称导电模型优于阿尔奇方程,不但可以描述纯砂岩阿尔奇规律,而且可以描述纯砂岩非阿尔奇规律,并且满足当孔隙度等于1时地层因素等于1,以及当含水饱和度等于1时电阻增大系数等于1的物理约束,可更好地描述纯砂岩导电规律.其次,针对分散泥质砂岩,使用有效介质对称导电理论建立泥质砂岩有效介质对称导电模型,理论分析与实验研究表明,泥质砂岩有效介质对称导电模型优于泥质电阻率模型和双电层模型,不需要采用经验拟合就能完整地描述饱含水分散泥质砂岩的电导率与地层水电导率之间曲线和直线关系,模型预测的粘土含量和粘土电导率变化对岩石导电规律的影响与理论认识相符,可更好地描述分散泥质砂岩导电规律.第三,针对两组分混合介质,使用有效介质对称导电理论、并联导电理论、串联导电理论,分别建立了有效介质对称导电方程、并联导电方程、串联导电方程,理论比较表明有效介质对称导电理论与并联导电理论和串联导电理论均不等价,即当两种组分混合介质遵循并联或串联导电规律时,混合介质的导电规律不能用有效介质对称导电理论描述.有效介质对称导电理论能够描述骨架和水以及粘土均为连续项的岩石导电规律.它通过引入渗滤指数和渗滤速率几何参数来描述各种组份的连通性、表面的粗糙度、形状、润湿性等对岩石导电性的影响,因此,有效介质对称导电理论的适用性更广,可用于描述孔隙结构更复杂的高泥高钙砂岩储层的导电规律. 相似文献
9.
10.
为了解用电阻率法、电磁法和激发极化法监测地下水污染的可能性,给出了在水样和含水砂样中,加入了不同浓度的无机污染物和有机污染物时,样品电阻率、极化率、半衰时和偏离度等导电性和激电性参数与浓度变化关系的几个实验观测结果．水样中的观测结果表明,除个别有机污染样品的电阻率随浓度增加有所增大外,其余所有无机污染和有机污染样品的电阻率均随浓度的增加而减小．含水砂样中的观测结果表明,不同污染成分样品的电阻率和极化率,均随孔隙液浓度的增加而减小,但对反应样品激电时间特性的参数而言,则有半衰时随浓度增加而减小,偏离度随浓度增加而增大的规律．同时指出,用电阻率法、电磁法和激发激化法监测地下水污染是十分困难的． 相似文献
11.
Spectral induced polarization as well as complex electrical measurements are used to estimate, on a non-invasive basis, hydraulic permeability in aquifers. Basic laboratory measurements on a variety of shaly sands, silts and clays showed that the main feature of their conductivity spectra in the frequency range from 10-3 to 103 Hertz is a nearly constant phase angle. Thus, a constant-phase-angle model of electrical conductivity is applied to interpret quantitatively surface and borehole spectral induced polarization measurements. The model allows for the calculation of two independent electrical parameters from only one frequency scan and a simple separation of electrical volume and interface effects. The proposed interpretation algorithm yields the true formation factor, the cation exchange capacity and the surface-area-to-porosity ratio, which corresponds to the inverse hydraulic radius. Using a Kozeny–Carman-like equation, the estimation of hydraulic permeability is possible. 相似文献
12.
Mohamed Mahmoud Gomaa 《Geophysical Prospecting》2009,57(6):1091-1100
This paper is devoted to study the effect of saturation, with distilled water, on AC electrical conductivity and dielectric constant of a fully and partially saturated hematitic sandstone sample (Aswan area, Egypt). The saturation of the sample was changed from full saturation to partial saturation by air drying. Complex resistivity measurements at room temperature (∼16° C) were performed in the frequency range from 10 Hz to 100 kHz. We used non-polarizing Cu/CuSO4 gel electrodes. Experimental electrical spectra indicate, generally, that the electrical conductivity and dielectric constant vary strongly with water saturation and frequency. The low-frequency electrical conductivity and dielectric constant are supposed to be mainly controlled by surface conduction and polarization of the electrical double layer. Power law behaviours with frequency were noticed. The change in electrical conductivity and dielectric constant with increasing water content is fast at low saturations and slow at high saturations. The behaviour of the electrical conductivity and dielectric constant, with increasing water content, was argued to be the orientational polarization of bound water for very low saturations, displacement of the excess surface charges for relatively low saturations and free exchange of excess ions in double layer with the bulk electrolyte and generation of transient diffusional potentials, which lag behind the applied field for high saturations in addition to membrane polarization on clay and at inter-grain and grain surface water throats having selective charge transport properties. Also, from the data a semi-percolation behaviour was found that has a peak of dielectric constant at a certain concentration and an abrupt change in conductivity at another saturation. 相似文献
13.
复电阻率测井在识别油水层的能力上优于常规电阻率测井,然而储层岩石复电阻率特性的微观机理还没有统一完整的解释和数学模拟方法,致使复电阻率测井技术的开发缺乏足够的理论基础.本文基于孔隙介质Pride电震耦合理论,结合谐变信号激励下渗流场与电流场的耦合理论,推导出一级近似条件下的Pride电震耦合理论.采用格林函数方法建立了一维电震波场的波动方程及其解.构造了双电极法测量储层岩石复电阻率的物理模型和数学模型,从理论上阐明了岩石复电阻率频散特性的微观机制与电震效应的关系,定量分析了储层岩石复电阻率频散特性的影响因素.数学模拟结果表明:储层岩石复电阻率的频散现象是在电震快纵波和电震慢纵波的共同作用下,由孔隙介质中的电渗流机制形成的;储层岩石的复电阻率随孔隙度的增大而减小,随渗透率的增大而增大,地层水矿化度的增加或阳离子交换量的增大使得同频率的复电阻率减小.慢纵波界面极化频率受孔隙度、渗透率和地层弹性模量的影响较大,而快纵波界面极化频率受地层弹性模量的影响较大. 相似文献
14.
液相渗透率描述了岩石的渗流特性,是评价储层与预测油气产能的重要参数.液相渗透率是指盐水溶液在岩石孔隙中流动且与岩石孔隙表面黏土矿物发生物理化学作用时所测得的渗透率;液相渗透率的实验测量条件更加接近实际地层泥质砂岩的条件,使得液相渗透率更能反映地层条件下泥质砂岩的渗流特性;然而,现有的液相渗透率评价模型较少,且模型未能揭示液相渗透率与溶液矿化度之间的关系.基于此,开展了液相渗透模型推导与计算方法研究;文中首先将岩石等效为毛管束模型,推导建立了液相渗透率与比表面、喉道曲折度、总孔隙度、黏土束缚水孔隙度等参数之间的关系;其次,根据岩石物理体积模型,推导建立了黏土束缚水孔隙度与阳离子交换容量、溶液矿化度等参数的关系;最终,将黏土束缚水孔隙度引入液相渗透率计算公式,建立了基于总孔隙度、阳离子交换容量、溶液矿化度、比表面、喉道曲折度等参数的液相渗透率理论计算模型.液相渗透率计算模型与两组实验数据均表明,液相渗透率随阳离子交换容量的增大而降低,随溶液矿化度的增大而增大.然而,液相渗透率理论计算模型的实际应用中喉道曲折度、比表面等参数求取困难,直接利用理论模型计算液相渗透率受到限制.在分析液相渗透率与孔隙渗透率模型的基础上,建立了液相渗透率与空气渗透率之间的转换模型,形成了利用转化模型计算液相渗透率的新方法.为进一步验证液相渗透率与空气渗透率转化模型的准确性,基于两组实验数据,利用转换模型计算了液相渗透率;液相渗透率计算结果与岩心测量液相渗透率实验结果对比显示,液相渗透率计算结果与实际岩心测量结果吻合较好,文中建立的液相渗透率与空气渗透率转化模型合理可靠. 相似文献
15.
井-地与井间电位技术联合数值模拟研究剩余油分布(英文) 总被引：5，自引：2，他引：3
电法测井有很高的分辨率,但是它的探测半径仅限于井孔周围;井-地电位技术虽然可以探测到足够大的范围,但是它的分辨率却受到很大的限制,特别是对于油水分布或者结构复杂的储层。本文试图通过井-地电位技术和井间电位技术的联合来研究地下储层油水分布范围。具体方法是,采用井-地电位技术研究油水分布在在横向上的展布情况,利用井间电位技术研究油水储层在垂向上的分布,然后采用井间电位结果标定井地电位结果,两者结合提高纵向分辨率,从而确定剩余油的三维空间分布。研究中通过研究注水初期数值模拟结果与水淹期数值模拟结果之差,求取剩余油分布范围。有限差分方法数值模拟表明:井-地电位技术与井间电位技术联合方法可以有效地确定剩余油分布。 相似文献
16.
《Acta Geochimica》2017,(1)
A study was conducted by collecting eight seepage water samples that drain through the sedimentary rocks,mainly sandstone and shale,to evaluate the hydrogeochemical characteristics.The collected samples were analyzed for physico-chemical parameters using standard procedures.Three water types were identified in the Piper plot and the hydrogeochemical evolution starts from a CaCl facies(type 1) via mixed Ca-Mg-Cl and Ca-Na-HCO_3 facies(type 2) to Na-Cl facies(type 3).Increasing trend of electrical conductivity(EC) values were observed from type 1 water to type 3 water.Lower ionic concentrations with an average EC value of 35.7(is/cm in Ca-Cl facies indicate the recharge water by monsoonal rainfall,and ion exchange/weathering process is reflected in the mixing zone.Higher ionic concentration with an average EC value of 399(is/cm is noted in Na-Cl facies,which indicates the ion exchange during water-rock interaction.Higher log PCO_2 values are also found in this facies,revealing the longer residence time of seepage water in the rock matrix,which release more ions into the water.The relative mobility of elements during weathering suggest that the order of mobility in both sandstone and shale is Na Ca Mg K.It was observed that the hydrogeochemistry of seepage water is mainly controlled by the bedrock geology. 相似文献
17.
The results of research on the pollutant retardation potential of permeable riverbed sediments in catchments with significant groundwater–surface water (GW-SW) interaction are presented. The fraction of organic carbon and cation exchange capacity of fluvial sediments in various geomorphologic environments have been quantified. Sediments in selected reaches of the rivers Tern and Leith (UK), from the underlying Permian sandstone aquifers, and from along the length of the rivers Severn and Eden into which the Tern and Leith discharge have been investigated. Statistical analyses show significant variation in the geochemistry and pollutant retardation potential of sediments from different geomorphologic features, and between upland and lowland rivers. The sorption potential of fine-grained sediments deposited in pools was greater than sand in runs and coarser deposits in riffles. Similarly, sediments in lowland rivers were found to have a greater retardation potential than those in upland rivers. There was generally greater retardation potential in fluvial sediments of all types than in the underlying aquifers, and in lowland rivers the fluvial sediment retardation potential greatly dominated that of the aquifer. The findings demonstrate the potential for pollutant retardation processes in riverbed sediments of sandstone catchments, and suggest that consideration of retardation processes at the groundwater–surface water interface should be included into environmental risk-assessment studies, in order to better assess and manage the effects of contaminated groundwater discharges to rivers, particularly in lowland catchments. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
18.
Bogadi T. Mathangwane Mark A. Chappell Jutta R. V. Pils Leticia S. Sonon Vasilos P. Evangelou 《洁净——土壤、空气、水》2008,36(2):201-208
Critics charge that agricultural managers routinely overdose their fields with chemical N and P to levels that exceed the soil's capacity to adsorb these materials, creating a situation that promotes hypoxia in Iowa lakes. Soil colloidal particles, capable of forming complexes with inorganic and organic N and P, control the equilibrium concentration of dissolved nutrients in lake waters. However, it should be realized that adsorbed nutrients also exhibit strong influences on the potential of sediments to undergo dispersion, a condition that may directly impact nutrient bioavailability. Thus, direct links may exist between adsorbed nutrient compositions and flocculation/dispersion properties of lake colloidal material. This paper presents work involving four Iowa lakes undertaken to determine relationships between ion composition and the dispersion potential of sediments. Surface waters and lake‐bottom grab samples were collected at three separate collection times from August to October. Samples were characterized for dissolved and adsorbed cations. Dispersion potential of each water sample was characterized by relating the total suspended solids concentration to the absorbance at 560 nm. It was found that sediment dispersion was easily predictable by a simple yet significant linear correlation with the concentration ratio of Na (CRNa = [Na]/[Ca]–1/2) in solution. This correlation was further improved by including Na concentration, CRK, electrical conductivity, temperature, and solution P concentrations into the model. Nonlinear inter‐dependences were found between TSS and cation exchange capacity (CEC), and adsorbed Na, K, P, and heavy metals. Our analysis suggests that solution/solid phase constituents influenced the dispersion behavior of sediments through subtle manipulations of the excess surface charge. 相似文献