Probing the adsorption behavior and molecular interactions of asphaltene subfractions at Water–Toluene/Heptol interface

作者：Hongtao Ma, Diling Yang, Zuoli Li, Yongxiang Sun, Ying Hu, Xiaohui Mao, Baoshan Lu, Hao Zhang, Hongbo Zeng · 发表于：Fuel · 年份：2025 · DOI：10.1016/j.fuel.2025.134577 · 被引用次数：8 · 研究领域：Petroleum Processing and Analysis、Hydrocarbon exploration and reservoir analysis、Enhanced Oil Recovery Techniques

Asphaltene-stabilized water-in-oil (W/O) emulsions present significant challenges, contributing to corrosion and fouling in the oil industry. Previous studies have suggested that only a small fraction of asphaltenes is responsible for emulsion stabilization. In this work, whole asphaltenes were fractionated into interfacially active (IAA) and non-active (INAA) subfractions to better understand their interfacial behaviors. Dynamic interfacial tension (IFT), Langmuir–Blodgett trough, atomic force microscopy (AFM) imaging, and AFM drop probe technique were employed to explore the adsorption behavior, interfacial film properties, and interaction forces of IAA and INAA asphaltenes at the water-toluene/heptol interface. The effects of asphaltene subfraction concentrations and solvent aromaticity were systematically evaluated. IAA asphaltenes manifested higher interfacial diffusion coefficients and lower equilibrium interfacial tension at the water-toluene/heptol interface compared to INAA asphaltenes, indicating superior adsorption capabilities. IAA asphaltenes showed decreased interfacial diffusion coefficients at the water-heptol interface compared to toluene, while INAA asphaltenes displayed the opposite trend. Asphaltene subfractions formed protective layers at the water-toluene/heptol interface, sterically inhibiting water droplet coalescence. IAA asphaltenes form more rigid interfacial films than INAA asphaltenes, with the addition of n -heptane further increasing film rigidi...