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Charge Control And Wettability Alteration At Solid-liquid Interfaces

机译:固液界面的充电控制和润湿性改变

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Most solid surfaces acquire a finite surface charge upon exposure to aqueous environments due to desorption and/or adsorption of ionic species. The resulting electrostatic forces play a crucial role in many fields of science, including colloidal stability, self-assembly, wetting, and biophysics as well as technology. Enhanced oil recovery is an example of a large scale industrial process that hinges in many respects on these phenomena. In this paper, we present a series of experiments illustrating fundamental aspects of low salinity water flooding in well- defined model systems. We show how pH and ion content of the water phase as well as the presence of model polar components (fatty acids) in the oil phase affect the wettability (i.e. contact angle distribution) of oil-water-rock systems. Specifically, we discuss high resolution atomic force microscopy (AFM) experiments demonstrating the preferential adsorption of multivalent cations to mineral surfaces such as mica and gibbsite. Cation adsorption leads to increased and in some cases reversed surface charge at the solid-liquid interface. In the case of charge reversal, the adsorption process can trigger a wetting transition from complete water wetting in ambient oil (i.e. zero water contact angle) in the absence to partial wetting in the presence of divalent cations. While already dramatic for pure alkanes as base oil, adding fatty acids to the oil phase enhances the effect of divalent ions on the oil-water-rock wettability even more. In this case, contact angle variations of more than 70° can be observed as a function of the salt concentration. This enhancement is caused by the deposition of a thin film of fatty acid on the solid surface. AFM as well as surface plasmon resonance spectroscopy measurement in a microfluidic continuous flow cell directly demonstrate that adsorbed Ca ions promote secondary adsorption of acidic components from the oil phase. The combination of the effects discussed provides a rational scenario explaining many aspects of the success of low salinity water flooding.
机译:由于离子物质的解吸和/或吸附,大多数固体表面在暴露于水性环境时获得有限表面电荷。由此产生的静电力在许多科学领域发挥着至关重要的作用,包括胶体稳定性,自组装,润湿和生物物理学以及技术。增强的石油回收是大规模工业过程的一个例子,即在许多方面铰接在这些现象中。在本文中,我们提出了一系列实验,说明了在明确的模型系统中的低盐水洪水的基本方面。我们展示了水相的pH和离子含量以及油相中模型极性成分(脂肪酸)的存在影响油 - 水岩系的润湿性(即接触角分布)。具体地,我们讨论高分辨率原子力显微镜(AFM)实验,证明了多价阳离子对矿物表面的优先吸附,例如云母和胶束。阳离子吸附导致在某些情况下升高,在固体液体界面处反转表面电荷。在电荷逆转的情况下,吸附过程可以在不存在于二价阳离子的情况下触发环境油(即零水接触角)中的完全水润湿的润湿过渡。虽然已经使纯烷烃作为基础油的戏剧性,但向油相加入脂肪酸增强了二价离子对油岩润湿性的影响。在这种情况下,可以观察到大于70°的接触角变化作为盐浓度的函数。这种增强是由在固体表面上沉积脂肪酸的薄膜引起的。 AFM以及表面等离子体共振光谱测量在微流体连续流动细胞中直接证明吸附的Ca离子促进来自油相的酸性组分的二次吸附。所讨论的效果的组合提供了一种理性场景,解释了低盐水洪水成功的许多方面。

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