Zhao Xuezhi, Zhan Fuxing, Liao Guangzhi, Liu Weidong, Su Xin, Feng Yujun
Polymer Research Institute, State Key Laboratory of Polymer Materials Engineering, Sichuan University, Chengdu 610065, People's Republic of China.
PetroChina Exploration & Production Company, Beijing 100007, People's Republic of China.
J Colloid Interface Sci. 2022 Aug 15;620:465-477. doi: 10.1016/j.jcis.2022.04.045. Epub 2022 Apr 11.
It is generally believed that the improved efficiency of surfactant enhanced oil recovery (EOR) comes from ultra-low interfacial tension (IFT) between oil and surfactant solution owing to the formation of middle-phase microemulsion. However, hindered visibility in underground porous media prevents direct observation of in situ generation of middle-phase microemulsion during surfactant flooding. Thus, direct visualization of the process is vital, and could clarify its contribution to EOR.
Micro-emulsification of a displacing fluid containing sodium 4-dodecylbenzenesulfonate and alcohol propoxy sulfate with model oil was investigated. Phase diagrams were drawn using salinity scans, and the influence of polymer on emulsification was analyzed. Micro-emulsification was monitored through in situ fluorescent tagging via 2D-microfluidics and ex situ visualization via cryo-electron microscopy and small angle X-ray scattering. Its contribution to the oil recovery factor was quantified by measuring the volume of each phase in the eluates.
On-chip experiments indicated that in situ micro-emulsification occurred when the prescreened surfactant solution flowed in contact with trapped oil. The aqueous phase initially invaded the residual oil, forming a low mobility microemulsion. This microemulsion was then diluted by subsequent displacing fluid, forming a new driving fluid that caused ultra-low IFT in the trapped oil downstream. Under the synergistic effect of micellar solubilization and trapped-oil mobilization, the recovery factor could be increased by up to 40% over waterflooding and 43% on polymer inclusion in the formulation.
人们普遍认为,表面活性剂强化采油(EOR)效率的提高源于中间相微乳液的形成,使得油与表面活性剂溶液之间具有超低界面张力(IFT)。然而,地下多孔介质中能见度受阻,妨碍了在表面活性剂驱油过程中原位生成中间相微乳液的直接观测。因此,对该过程进行直接可视化至关重要,这可能会阐明其对EOR的贡献。
研究了含4-十二烷基苯磺酸钠和醇醚硫酸酯的驱替液与模拟油的微乳化作用。通过盐度扫描绘制相图,并分析了聚合物对乳化的影响。通过二维微流控原位荧光标记以及低温电子显微镜和小角X射线散射的非原位可视化来监测微乳化过程。通过测量洗脱液中各相的体积来量化其对采收率的贡献。
芯片实验表明,当预先筛选的表面活性剂溶液与捕集油接触流动时,会发生原位微乳化。水相最初侵入残余油,形成低流动性微乳液。然后该微乳液被后续驱替液稀释,形成一种新的驱动液,在下游捕集油中产生超低IFT。在胶束增溶和捕集油 mobilization 的协同作用下,采收率可比水驱提高高达40%,在配方中加入聚合物时提高43%。 (注:原文中“trapped-oil mobilization”的“mobilization”可能有误,推测可能是“mobilization”,暂按此翻译,若有误请根据正确内容调整)