石油炼制与化工 ›› 2026, Vol. 57 ›› Issue (1): 49-57.

• 基础研究 • 上一篇    下一篇

聚电解质改性氧化石墨烯的耐盐机制及其与表面活性剂的协同洗油性能

乔富林,秦冰,江建林,申玉坦   

  1. 中石化石油化工科学研究院有限公司
  • 收稿日期:2025-07-28 修回日期:2025-08-24 出版日期:2026-01-12 发布日期:2025-12-23
  • 通讯作者: 秦冰 E-mail:qinbing.ripp@sinopec.com
  • 基金资助:
    CO2微气泡/两亲聚合物在稠油化学降黏复合驱中协同作用机制研究;金属表面多级组装结构的可控构筑及其长效缓蚀机制研究

SALT-TOLERANT MECHANISM OF POLYELECTROLYTE-MODIFIED GRAPHENE OXIDE AND ITS SYNERGISTIC OIL WASHING PERFORMANCE WITH SURFACTANTS

  • Received:2025-07-28 Revised:2025-08-24 Online:2026-01-12 Published:2025-12-23

摘要: 氧化石墨烯纳米材料在三次采油领域的应用备受关注,但如何提高材料在含盐地层水中的稳定性成为目前亟待攻克的技术问题。通过原子力显微镜、动态光散射等手段表征了氧化石墨烯纳米片的形貌及尺寸等特征,并研究了单宁酸、小分子有机酸盐以及大分子聚电解质对纳米片状氧化石墨烯(GO)在含盐水中稳定性的影响。结果表明,作为大分子聚电解质,聚丙烯酸钠(PAA)具有适宜的电荷密度与亲/疏水性,能够通过非共价作用吸附于GO表面,有效增强改性GO之间的静电排斥,对材料在含盐水中的稳定效果最佳。当PAA加入质量浓度为150 mg/L时,可使GO在质量浓度为10 000 mg/L的氯化钠水溶液中稳定24 h。PAA改性氧化石墨烯(PAA/GO)能够与阴离子表面活性剂协同作用,提高阴离子表面活性剂对稠油的适应性,起到强化乳化降黏效果。同时,超高的比表面积使得PAA/GO纳米材料高效吸附于油/水界面并产生结构分离压力,有效推动油/固两相分离。在上述双重增效机制下,PAA/GO纳米材料在10 mg/L的低质量浓度下即可将阴离子型表面活性剂的洗油效率提高2.1倍。然而,由于非离子表面活性剂在纳米材料表面的吸附能力过强,削弱了其在油/水界面的乳化作用,导致PAA/GO和非离子表面活性剂复合体系的洗油效率反而低于非离子表面活性剂单一体系。

关键词: 氧化石墨烯, 聚电解质, 耐盐能力, 洗油性能

Abstract: The application of graphene oxide nanomaterials in tertiary oil recovery has garnered considerable interest, yet improving their stability in saline formation water remains a critical technical challenge. This study characterized the morphology and dimensions of graphene oxide (GO) nanosheets using atomic force microscopy and dynamic light scattering, while systematically investigating the stabilization effects of tannic acid, small-molecule organic acid salts, and macromolecular polyelectrolytes on GO nanosheets in saline environments. Results showed that sodium polyacrylate (PAA), a macromolecular polyelectrolyte with optimized charge density and amphiphilicity, exhibited superior stabilization performance through efficient adsorption onto GO surfaces via non-covalent interaction and thus effectively enhanced the electrostatic repulsion between GO nano-sheets. At a concentration of 150 mg/L, PAA enabled GO to maintain stability for 24 h in 10 000 mg/L sodium chloride solution. The PAA-modified graphene oxide demonstrated synergistic interaction with anionic surfactant viscosity reducers, enhancing their adaptability to heavy oil and amplifying emulsification-based viscosity reduction. Meanwhile, the extremely high specific surface area enables PAA-modified graphene oxide to efficiently adsorb at the oil/water interface and generate structural seperation pressure, promoting the seperation of oil and solid phases. Under the dual enhancement mechanism above, PAA-modified graphene oxide can increase the oil removal efficiency of anionic surfactants by 2.1 times at a low concentration of 10 mg/L. However, excessive adsorption capacity of nonionic surfactants on nanomaterial surfaces was found to compromise emulsification at oil-water interfaces, resulting in lower oil-washing efficiency for the mixed systems compared to single surfactant systems.

Key words: graphene oxide, polyelectrolyte, salt-tolerant capacity, oil-washing performance