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Seawater Injection into Clastic Formations: Formation Damage Investigation Using Simulation and Coreflood Studies

机译:海水注射到碎片形成:使用模拟和核心研究的形成损害调查

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Waterflooding in different reservoirs for pressure maintenance and recovering more oil is a well established practice in oil industry. Many research studies have shown that the success of any waterflooding process is mainly dependent on both physicochemical (fluid-rock) and geochemical (fluid-fluid) interactions. These interactions have been extensively investigated during seawater injection into carbonate formations. However, the rock/seawater chemical interactions are completely different in sandstone than in carbonate formations, due to different rock mineralogy. Therefore, the main objective of this paper is to investigate both the potential physicochemical and geochemical formation damage mechanisms that might occur during injection of seawater into a central Arabia sandstone formation. Scaling potential due to seawater-produced brine chemical interactions was investigated at reservoir average temperature of 186°F, based on Pitzer theory of electrolytes. In addition to the prediction data, laboratory compatibility tests were conducted to investigate the scaling potential in different seawater/produced brine mixtures at reservoir temperature. Since this sandstone formation contained different clays such as illite and smectite, the clay swelling and fines migration tendency was explored using coreflood setup and zeta potential technique. The saturation index (SI) of different scales such as calcium carbonate and calcium sulfate was found to be mainly dependent on seawater/produced brine mixing ratio. Additionally, it was found that scaling did not occur in supersaturated mixtures of seawater, aquifer water and produced brine, which indicated that there is a critical SI for the scaling onset. Zeta potential for different formation rocks was determined for sweater, aquifer and produced brine. It was nearly zero when using only seawater. One of the major findings of this study is that the presence of sulfate ions caused clay particles to migrate even in high TDS seawater of nearly 55,000 ppm.
机译:在不同水库的水上塑造,用于压力维护和恢复更多的石油是石油工业中成熟的实践。许多研究研究表明,任何水上型过程的成功主要取决于物理化学(流体岩)和地球化学(流体流体)相互作用。在海水注射到碳酸盐形成期间,这些相互作用已被广泛研究。然而,由于不同的岩石矿物学,岩石/海水化学相互作用比碳酸盐形成完全不同。因此,本文的主要目的是探讨在将海水注入中央阿拉伯砂岩地层期间可能发生的潜在物理化学和地球化学形成机制。基于电解质理论,在186°F的储层平均温度下研究了由于海水产生的盐水化学相互作用导致的缩放电位。除了预测数据之外,还进行了实验室相容性测试,以研究在储层温度下不同海水/产生的盐水混合物中的缩放电位。由于这种砂岩形成含有不同的粘土,例如伊利石和蒙脱石,因此使用CoreFlood设置和Zeta潜在技术探索了粘土溶胀和鳍迁移趋势。发现不同鳞片的饱和指数(Si),例如碳酸钙和硫酸钙,主要取决于海水/产生的盐水混合比。此外,发现缩放不会发生在海水,含水层水和产生的盐水的过饱和混合物中,这表明缩放发作有一个关键的Si。针对毛衣,含水层和生产的盐水测定不同形成岩石的Zeta电位。仅使用海水时几乎是零。本研究的主要发现之一是硫酸根离子的存在使粘土颗粒甚至在近55,000ppm的高达TDS海水中迁移。

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