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Understanding the Cation-Dependent Surfactant Adsorption on Clay Minerals in Oil Recovery

机译:了解石油开采中阳离子依赖的表面活性剂对粘土矿物的吸附

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摘要

Surfactants have the ability to mobilize residual oil trapped in pore spaces of matrix rocks by lowering the oil water interfacial tension, resulting in a higher oil recovery. However, the loss of surfactants by adsorption onto the rock surface has become a major concern that reduces the efficiency of the surfactant flooding process. In this study, the adsorption behavior of an anionic surfactant to a clay mineral surface was investigated by quartz crystal microbalance with dissipation monitoring upon variations with different cation conditions. Through recording the change of frequency and dissipation of clay-modified sensors, it allows us to do a real-time quantitative analysis of the surfactant adsorption with nanogram sensitivity. The results revealed that the surfactant adsorption increased in a Ca2+-containing solution with increasing pH from 6 to 11, whereas from a Na+-containing solution, more adsorption occurred at acidic conditions. The adsorbed amount went through a maximum (similar to 200 mM) as a function of the Ca2+ concentration, and the Voigt model suggested that multilayer adsorption of surfactants could be as many as 4-6 monolayers. Using mixed cation (Ca2+ and Na+) solutions, the amount of adsorbed surfactant decreased linearly with decreasing fraction of CaCl2, but Na+ competed for about similar to 30% adsorption sites. The importance of the presence of CaCl2 for the surfactant adsorption was stressed in high-salinity and low-salinity solutions in the presence and absence of Ca2+. Furthermore, increasing the temperature from 23 to 65 degrees C shows first a small increase of surfactant adsorption followed by a reduction of about 20%. The obtained results contribute to a better understanding of surfactant adsorption on clay surfaces and a guide to optimal flooding conditions with reduced surfactant loss.
机译:表面活性剂具有通过降低油水界面张力而动员滞留在基质岩石孔隙中的残余油的能力,从而导致较高的油采收率。然而,由于吸附到岩石表面上而导致的表面活性剂的损失已经成为降低表面活性剂驱油工艺效率的主要问题。在这项研究中,通过石英晶体微量天平,通过耗散监测不同阳离子条件的变化,研究了阴离子表面活性剂在粘土矿物表面的吸附行为。通过记录粘土改性传感器的频率和耗散变化,它使我们能够以纳克灵敏度对定量的表面活性剂进行实时定量分析。结果表明,在含Ca2 +的溶液中,随着pH从6增加到11,表面活性剂的吸附增加,而在含Na +的溶液中,在酸性条件下吸附更多。吸附量随Ca2 +浓度的变化而达到最大值(约200 mM),而Voigt模型表明,表面活性剂的多层吸附可多达4-6个单层。使用混合阳离子(Ca2 +和Na +)溶液,表面活性剂的吸附量随CaCl2分数的降低而线性降低,但Na +竞争约30%的吸附位。在存在和不存在Ca2 +的高盐度和低盐度溶液中,强调了存在CaCl2对于表面活性剂吸附的重要性。此外,将温度从23摄氏度提高到65摄氏度首先显示出表面活性剂吸附量略有增加,然后降低了约20%。获得的结果有助于更好地理解表面活性剂在粘土表面的吸附,并为降低表面活性剂损失的最佳驱油条件提供了指导。

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  • 来源
    《Energy & fuels》 |2019年第12期|12319-12329|共11页
  • 作者单位

    Delft Univ Technol Fac Appl Sci Dept Chem Engn Organ Mat & Interfaces Van der Maasweg 9 NL-2629 HZ Delft Netherlands;

    Delft Univ Technol Dept Precis & Microsyst Engn Fac Mech Maritime & Mat Engn Mekelweg 2 NL-2628 CD Delft Netherlands;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
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