Angela C.P. Duncke , Camila N.R. Amaral , Mônica Netto , Gabriel G. de Barros , Paulo R. de Souza Mendes , Aurora Pérez-Gramatges
{"title":"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","authors":"Angela C.P. Duncke , Camila N.R. Amaral , Mônica Netto , Gabriel G. de Barros , Paulo R. de Souza Mendes , Aurora Pérez-Gramatges","doi":"10.1016/j.fuel.2025.137158","DOIUrl":null,"url":null,"abstract":"<div><div>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.</div></div>","PeriodicalId":325,"journal":{"name":"Fuel","volume":"406 ","pages":"Article 137158"},"PeriodicalIF":7.5000,"publicationDate":"2025-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Coupled effects of sulfonated PAM concentration and degradation on separation kinetics of oil/water emulsions: interplay of flocculation, viscosity, and homogenization\",\"authors\":\"Angela C.P. Duncke , Camila N.R. Amaral , Mônica Netto , Gabriel G. de Barros , Paulo R. de Souza Mendes , Aurora Pérez-Gramatges\",\"doi\":\"10.1016/j.fuel.2025.137158\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>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.</div></div>\",\"PeriodicalId\":325,\"journal\":{\"name\":\"Fuel\",\"volume\":\"406 \",\"pages\":\"Article 137158\"},\"PeriodicalIF\":7.5000,\"publicationDate\":\"2025-10-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Fuel\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0016236125028832\",\"RegionNum\":1,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENERGY & FUELS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fuel","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0016236125028832","RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
Coupled effects of sulfonated PAM concentration and degradation on separation kinetics of oil/water emulsions: interplay of flocculation, viscosity, and homogenization
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.
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.