Zhang Yandong, Geng Jiaming, Liu Junchen, Bai Baojun, He Xiaoming, Wei Mingzhen, Deng Wen
Department of Geosciences and Geological and Petroleum Engineering, Missouri University of Science and Technology, Rolla 65409 Missouri, United States.
Department of Mathematics and Statistics, Missouri University of Science and Technology, Rolla 65409 Missouri, United States.
Langmuir. 2021 Nov 16;37(45):13353-13364. doi: 10.1021/acs.langmuir.1c02029. Epub 2021 Nov 1.
Different from inorganic nanoparticles, nanosized cross-linked polymeric nanoparticles (nanogels) have been demonstrated to generate more stable Pickering emulsions under harsh conditions for a long term owing to their inherent high hydrophilicity and surface energy. In both core and pore scales, the emulsions are found to be able to form in situ during the nanofluid flooding process for an enhanced oil recovery (EOR) process. Due to the limitation of direct visualization in core scale or deficient pore geometries built by two-dimensional micromodels, the in situ emulsification by nanofluids and emulsion transport are still not being well understood. In this work, we use a three-dimensional transparent porous medium to directly visualize the in situ emulsification during the nanogel flooding process for EOR after water flooding. By synthesizing the nanogel with a fluorescent dye, we find the nanogels adsorbed on the oil-water interface to lower the total interfacial energy and emulsify the large oil droplets into small Pickering oil-in-water emulsions. A potential mechanism for in situ emulsification by nanogels is proposed and discussed. After nanogel flooding, the emulsions trapped in pore throats and those in the effluents are all found encapsulated by the nanogels. After nanogel flooding under different flow rates, the sphericity and diameter changes of remaining oil droplets are quantitatively compared and analyzed using grouped boxplots. It is concluded that in situ emulsification happens during nanogel injection due to the reduction of interfacial tension, which helps to increase the oil recovery rate under different flow rates and pore geometries.
与无机纳米颗粒不同,纳米尺寸的交联聚合物纳米颗粒(纳米凝胶)已被证明由于其固有的高亲水性和表面能,能够在恶劣条件下长期产生更稳定的皮克林乳液。在岩心和孔隙尺度上,发现乳液能够在纳米流体驱油过程中原位形成,以提高采收率(EOR)。由于在岩心尺度上直接可视化的局限性或二维微模型构建的孔隙几何形状不足,纳米流体的原位乳化和乳液运移仍未得到很好的理解。在这项工作中,我们使用三维透明多孔介质直接可视化水驱后纳米凝胶驱油过程中用于提高采收率的原位乳化。通过用荧光染料合成纳米凝胶,我们发现纳米凝胶吸附在油水界面上,以降低总界面能,并将大油滴乳化成小的皮克林水包油乳液。提出并讨论了纳米凝胶原位乳化的潜在机制。纳米凝胶驱油后,发现被困在孔喉中的乳液和流出物中的乳液都被纳米凝胶包裹。在不同流速下进行纳米凝胶驱油后,使用分组箱线图对剩余油滴的球形度和直径变化进行了定量比较和分析。得出的结论是,由于界面张力的降低,原位乳化在纳米凝胶注入过程中发生,这有助于在不同流速和孔隙几何形状下提高采收率。