Coupled effects of sulfonated PAM concentration and degradation on separation kinetics of oil/water emulsions: interplay of flocculation, viscosity, and homogenization

IF 7.5 1区 工程技术 Q2 ENERGY & FUELS
Fuel Pub Date : 2025-10-15 DOI:10.1016/j.fuel.2025.137158
Angela C.P. Duncke , Camila N.R. Amaral , Mônica Netto , Gabriel G. de Barros , Paulo R. de Souza Mendes , Aurora Pérez-Gramatges
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引用次数: 0

Abstract

In polymer Enhanced Oil Recovery (EOR), back-produced polymers can increase oil–water (O/W) emulsion stability, hampering phase separation and raising costs. In this EOR technique, high-molecular-mass polyacrylamides (PAMs) are commonly used, but under fixed shear production conditions, emulsions undergo the same homogenization and polymer degradation is unavoidable. This study systematically investigates the influence of sulfonated PAM (S-PAM) concentration and degradation on the phase separation kinetics of heavy O/W emulsions under reservoir-relevant conditions (high temperature, high salinity). The experimental approach quantified separation kinetics, bulk viscosity, oil–water interfacial properties, oil content, and droplet size distribution. A consistent, previously unreported inverted N-shaped relationship was observed between water release and polymer concentration for both intact and degraded S-PAM. Our findings reveal a dual mechanism governing this profile: at very low concentrations (≤ 10 ppm), polymer-bridging flocculation dominates, accelerating phase separation; at moderate concentrations, increased bulk viscosity and polymer steric stabilization hinder oil droplets creaming, decelerating phase separation by up to 1800 % compared to the polymer-free system. Above a critical concentration, the higher viscosity impairs homogenization, forming larger initial oil droplets that cream faster despite the viscous continuous phase, thereby re-accelerating separation. Degraded polymers exhibited slower phase separation and higher residual oil in the aqueous phase compared to intact counterparts. S-PAM showed no interfacial activity, and the proposed mechanisms were validated with a medium oil. These findings highlight the complex interplay between flocculation and viscosity effects in controlling O/W emulsion stability during polymer flooding, offering critical insights for optimizing produced water management strategies.
磺化PAM浓度和降解对油水乳液分离动力学的耦合影响:絮凝、粘度和均质化的相互作用
在聚合物提高采收率(EOR)中,返出的聚合物可以提高油水乳液(O/W)的稳定性,阻碍相分离,提高成本。在这种提高采收率技术中,通常使用高分子质量聚丙烯酰胺(pam),但在固定剪切生产条件下,乳液经过均匀化,聚合物降解是不可避免的。本研究系统研究了在油藏相关条件下(高温、高盐度)磺化PAM (S-PAM)浓度和降解对重油水乳状液相分离动力学的影响。实验方法量化了分离动力学、总体粘度、油水界面性质、含油量和液滴尺寸分布。在完整和降解的S-PAM中,水释放与聚合物浓度之间存在一致的倒n型关系。我们的研究结果揭示了控制这一特征的双重机制:在极低浓度(≤10 ppm)下,聚合物桥接絮凝起主导作用,加速相分离;在中等浓度下,增加的体粘度和聚合物立体稳定性会阻碍油滴形成奶油状,与无聚合物体系相比,相分离速度降低了1800%。在临界浓度以上,较高的粘度会损害均质性,形成更大的初始油滴,尽管存在粘性连续相,但油滴凝结速度更快,从而再次加速分离。与完整聚合物相比,降解聚合物表现出较慢的相分离和较高的水相剩余油。S-PAM没有界面活性,并在一种中等油中验证了所提出的机理。这些发现强调了在聚合物驱过程中,絮凝作用和粘度效应之间复杂的相互作用对控制油水乳状液稳定性的影响,为优化采出水管理策略提供了重要见解。
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来源期刊
Fuel
Fuel 工程技术-工程:化工
CiteScore
12.80
自引率
20.30%
发文量
3506
审稿时长
64 days
期刊介绍: The exploration of energy sources remains a critical matter of study. For the past nine decades, fuel has consistently held the forefront in primary research efforts within the field of energy science. This area of investigation encompasses a wide range of subjects, with a particular emphasis on emerging concerns like environmental factors and pollution.
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