Study on Oppositely Charged Polymer and Surfactant Mixture for Enhancing Oil Production

Limin Xu, M. Han, Xuan Zhang, A. Fuseni
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引用次数: 1

Abstract

Polymer-surfactant mixtures in aqueous solutions present unique rheological and interfacial properties that promote their applications in chemical flooding. The objective of this study is to investigate the interaction between anionic polyacrylamides and cationic surfactants in different temperature and salinity conditions and the potential application of the polymer-surfactant mixtures in carbonate reservoirs. Cationic surfactants were selected owing to low adsorption on carbonate rocks. Compatibility tests of polymer-surfactant mixtures were conducted in brine with different salinities to study the interaction between anionic polymers and cationic surfactants in the presence of salts. The effect of cationic surfactants on polymer viscosity at different temperatures was investigated. The compatibility of the mixtures of the cationic surfactants and the anionic polymers was significantly improved in high salinity injection water (with a total dissolved solid of 57,670 mg/L), compared with the compatibility in deionized water. This is attributed to the shielding of polymer and surfactant charges by the salts, which diminishes the electrostatic interaction between the chemicals. Rheological measurements indicated that the polymer viscosity increased in the presence of the cationic surfactant CAS-S or CAS-B. This effect was decreased at 90˚C. Other cationic surfactant CAS-1 or CAS-3 slightly increased the polymer viscosity at 25˚C and significantly decreased the viscosity at 90˚C. These observations can be explained based on the surfactants self-assembly. At room temperature, CAS-1 and CAS-3 form spherical micelles while CAS-S and CAS-B form wormlike micelles. The entanglement of the polymers with wormlike micelles explains the observed viscosity enhancement. At 90˚C, wormlike micelles became shorter which weakens this viscosity enhancement effect. In conclusion, the charges and self-assembly structures of surfactants play an important role in the performance of polymer-surfactant mixtures that should be taken into account in the design of optimal formulations. This work provides the insight of interaction between anionic polymers and cationic surfactants with different self-assembly structures for the potential application in improving oil production.
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极性聚合物与表面活性剂混合增油研究
聚合物-表面活性剂在水溶液中的混合物具有独特的流变性和界面特性,促进了它们在化学驱中的应用。研究了阴离子聚丙烯酰胺与阳离子表面活性剂在不同温度和盐度条件下的相互作用,以及聚合物-表面活性剂混合物在碳酸盐岩储层中的潜在应用。由于阳离子表面活性剂在碳酸盐岩上的吸附较低,因此选择了阳离子表面活性剂。在不同盐度的盐水中进行了聚合物-表面活性剂混合物的相容性试验,研究了阴离子聚合物与阳离子表面活性剂在盐存在下的相互作用。研究了不同温度下阳离子表面活性剂对聚合物粘度的影响。与去离子水相比,阳离子表面活性剂与阴离子聚合物的混合物在高矿化度注入水中(溶解固体总量为57,670 mg/L)的相容性得到了显著改善。这是由于盐对聚合物和表面活性剂电荷的屏蔽作用,从而减少了化学物质之间的静电相互作用。流变学测量表明,在阳离子表面活性剂CAS-S或CAS-B的存在下,聚合物粘度增加。这种效应在90℃时减弱。其他阳离子表面活性剂CAS-1或CAS-3在25℃时略微提高聚合物粘度,在90℃时显著降低聚合物粘度。这些观察结果可以根据表面活性剂的自组装来解释。在室温下,CAS-1和CAS-3形成球形胶束,CAS-S和CAS-B形成蠕虫状胶束。聚合物与蠕虫状胶束的纠缠解释了观察到的粘度增强。在90℃时,虫状胶束变短,使增粘效果减弱。综上所述,表面活性剂的电荷和自组装结构对聚合物-表面活性剂混合物的性能起着重要作用,在设计最佳配方时应考虑这些因素。这项工作提供了阴离子聚合物与具有不同自组装结构的阳离子表面活性剂之间相互作用的见解,为提高石油产量提供了潜在的应用。
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