Study on the Strong Association and Synergistic Temperature and Salt Resistance Mechanism of Differential Charge Surfactants and Ionic Polymer Systems

IF 3.6 4区 工程技术 Q2 ENGINEERING, CHEMICAL
Chengwei Zuo, Pingli Liu, Pengfei Chen, Gang Xiong, Xiaojiang Li, Zhenfu Jia
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引用次数: 1

Abstract

ABSTRACT The amphiphilic hydrophobic associative polyacrylamide (HAPAM) was synthesized via free radical copolymerization using hexadecyl allyl dimethyl ammonium chloride (C16DMAAC), acrylic acid (AA), acrylamide (AM), and 2‐acrylamido‐2‐methylpropanesulfonic acid (AMPS) as raw materials. Additionally, the oil amide sulfobetaine (OSB) amphoteric surfactant was synthesized from oil amide dimethyl tertiary amine, sodium sulfite (NaHSO 3 ), and epichlorohydrin. The impact of various charged surfactants (SDS, DTAB, OSB, and AEO) on the binding properties of HAPAM in NaCl solution was investigated through measurements of apparen t viscosity, dynamic light scattering, cryogenic scanning electron microscopy, and rheological analysis. The results indicated that the viscosity of HAPAM in NaCl solution exhibited a parabolic relationship, first rising and then falling, with increasing concentrations of SDS and OSB. Upon the addition of OSB, the temperature and shear resistance of the polymer system were significantly enhanced. Compared to the system before surfactant addition, the maximum viscosity increased by approximately 10 mPa (70%) after shearing at 120°C. At different concentrations of OSB and SDS, the viscosity increased by 133%–157%, the hydration radius of HAPAM expanded by 2.28 to 6.22 times, and the absolute value of the zeta potential increased by 27.66 mV. Microscopic morphological observations revealed that the polymer system formed a three‐dimensional network structure of intermolecular association with the addition of surfactants, ultimately creating a dense spatial structure. However, this phenomenon was not as pronounced for cationic and nonionic surfactants. These findings, corroborated by molecular dynamics simulations, confirmed that an appropriate amount of anionic surfactants can enhance hydrophobic binding, expand electrostatic repulsion between anions, and significantly improve the resistance and electrostatic shielding effect of HAPAM against salt solution compression bilayer. This study provides valuable insights into the effects of surfactants on the cross‐linking structure and binding properties of HAPAM in NaCl solution, offering guidance for improving the recovery rate in binary composite flooding applications.
差动电荷表面活性剂与离子聚合物体系的强缔合及增效耐温耐盐机理研究
摘要以十六烷基烯丙基二甲基氯化铵(C16DMAAC)、丙烯酸(AA)、丙烯酰胺(AM)和2‐丙烯酰胺‐2‐甲基丙磺酸(AMPS)为原料,采用自由基共聚法制备了两亲疏水缔合性聚丙烯酰胺(HAPAM)。此外,以油酰胺二甲基叔胺、亚硫酸钠(nahso3)和环氧氯丙烷为原料合成了油酰胺磺基甜菜碱(OSB)两性表面活性剂。通过表观粘度、动态光散射、低温扫描电镜和流变学分析,研究了不同表面活性剂(SDS、DTAB、OSB和AEO)对HAPAM在NaCl溶液中结合性能的影响。结果表明,随着SDS和OSB浓度的增加,HAPAM在NaCl溶液中的粘度呈先上升后下降的抛物线关系;加入OSB后,聚合物体系的耐温性和抗剪切性明显增强。与加入表面活性剂之前的体系相比,在120℃下剪切后的体系最大粘度增加了约10 mPa(70%)。在不同浓度的OSB和SDS下,HAPAM的黏度增加了133% ~ 157%,水化半径扩大了2.28 ~ 6.22倍,zeta电位绝对值增加了27.66 mV。微观形态观察表明,随着表面活性剂的加入,聚合物体系形成了分子间结合的三维网络结构,最终形成了致密的空间结构。然而,这种现象在阳离子和非离子表面活性剂中并不明显。这些发现得到了分子动力学模拟的证实,证实了适量阴离子表面活性剂可以增强疏水结合,扩大阴离子间的静电斥力,显著提高HAPAM对盐溶液压缩双分子层的抵抗力和静电屏蔽效果。该研究为研究表面活性剂对HAPAM在NaCl溶液中的交联结构和结合性能的影响提供了有价值的见解,为提高二元复合驱的采收率提供了指导。
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来源期刊
Polymer Engineering and Science
Polymer Engineering and Science 工程技术-高分子科学
CiteScore
5.40
自引率
18.80%
发文量
329
审稿时长
3.7 months
期刊介绍: For more than 30 years, Polymer Engineering & Science has been one of the most highly regarded journals in the field, serving as a forum for authors of treatises on the cutting edge of polymer science and technology. The importance of PE&S is underscored by the frequent rate at which its articles are cited, especially by other publications - literally thousand of times a year. Engineers, researchers, technicians, and academicians worldwide are looking to PE&S for the valuable information they need. There are special issues compiled by distinguished guest editors. These contain proceedings of symposia on such diverse topics as polyblends, mechanics of plastics and polymer welding.
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