Brine to Enhance the Transport of Encapsulated Petroleum Sulfonates Nanosurfactants Deeper into the High Temperature Carbonate Reservoirs

A. Gizzatov, Mohammed Kawelah, Afnan Mashat, A. Abdel-Fattah
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Abstract

Development of NanoSurfactants (NSs), encapsulated petroleum sulfonates, is in progress for use as one of the most cost efficient surfactants in chemical enhanced oil recovery (CEOR) applications under extreme conditions. This work provides a better understanding of NS transport though porous carbonate rocks and demonstrates how hot and salty brines can facilitate NS transport when compared to deionized (DI) water. Transport of NSs at 90 °C in 57,000 ppm total dissolved solids (TDS) brine as well as NS components, petroleum sulfonate and zwitterionic co-surfactant, in 90 °C DI water through limestone core plugs was studied using a core flood apparatus. Effluent samples were measured for the total surfactant concentration using a total organic carbon (TOC) analyzer, and the dynamic retention values were calculated and compared. Structural integrity of NS assemblies before and after transport through the porous rock structure were studied using 1H Nuclear Magnetic Resonance (NMR) spectroscopy. Petroleum sulfonate surfactants are unstable in hot brines with high concentrations of divalent ions, and therefore cannot be transported through porous rock structures. Transforming such unstable sulfonates into NS formulations can overcome these challenges. Dynamic retention results in water-wet limestone demonstrate that NSs can be successfully transported through 150 - 200 millidarcy (mD) reservoir rocks with retention values < 0.4 mg/g of rock. These values are 30-50% lower than the retention of NS components alone, which is < 0.7 mg/g, if measured at the same conditions using DI water. Much lower retention for NSs was observed in brines, when compared to its surfactant components in DI water. This can be attributed to the NSs nanostructure which is designed to encapsulate sulfonates closer to the core while efficiently dispersing in the brines by co-surfactants with zwitterionic heads located at the surface. High salinity brine also helps to screen surface charges present on the rock surface. NMR spectroscopy results confirm that the nano-assembled NS structure does not exhibit noticeable changes after core flood experiments and confirms that the formulation has great potential for CEOR applications. Results presented in this work demonstrate that NS formulations made of assembled and dispersed nanocapsules enable the application of one of the lowest cost industrial surfactants for CEOR in hot and salty brines. This formulation in brines significantly reduces the loss of surfactants to the carbonate rock when compared to the same surfactant components in fresh water.
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卤水促进包裹石油磺酸盐纳米表面活性剂向高温碳酸盐岩储层深层运移
纳米表面活性剂(NSs)是一种封装的石油磺酸盐,它是极端条件下化学提高石油采收率(CEOR)应用中最具成本效益的表面活性剂之一。这项工作提供了通过多孔碳酸盐岩运移的更好理解,并证明了与去离子水(DI)相比,热盐水和咸盐水如何促进NS的运移。采用岩心驱替装置,研究了90℃下57,000 ppm总溶解固体(TDS)盐水中NSs以及90℃DI水中NSs组分、石油磺酸盐和两性离子共表面活性剂通过石灰石岩心塞的运移。利用总有机碳(TOC)分析仪测定出水样品的表面活性剂总浓度,计算并比较动态保留值。采用1H核磁共振(NMR)技术研究了NS组件通过多孔岩石结构前后的结构完整性。石油磺酸盐表面活性剂在含有高浓度二价离子的热盐水中不稳定,因此不能通过多孔岩石结构进行输送。将这种不稳定的磺酸盐转化为NS配方可以克服这些挑战。水湿石灰岩的动态滞留结果表明,NSs可以成功地通过150 - 200毫达西(mD)储集岩,其滞留值< 0.4 mg/g。如果在相同条件下使用去离子水测量,这些值比单独使用NS组分的保留率低30-50%,其< 0.7 mg/g。与表面活性剂组分相比,NSs在盐水中的保留率要低得多。这可以归因于NSs纳米结构,该结构设计用于封装更靠近核心的磺酸盐,同时通过位于表面的两性离子头的共表面活性剂有效地分散在盐水中。高盐度盐水也有助于屏蔽岩石表面的表面电荷。核磁共振波谱结果证实,纳米组装的NS结构在岩心淹水实验后没有出现明显的变化,证实了该配方具有巨大的CEOR应用潜力。这项工作的结果表明,由组装和分散的纳米胶囊组成的NS配方可以在热盐水和盐水中应用成本最低的工业表面活性剂之一。与在淡水中使用相同的表面活性剂组分相比,盐水中的这种配方显著减少了表面活性剂在碳酸盐岩中的损失。
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