Novel polymer nanoparticles with core–shell structure for breaking asphaltenes-stabilized W/O and O/W emulsions

沥青质 破乳剂 乳状液 化学工程 甲苯 表面张力 纳米颗粒 聚合物 吸附 材料科学 油滴 化学 色谱法 有机化学 热力学 物理 工程类
作者
Xiaohui Mao,Feifei Wang,Baoshan Lu,Tian Tang,Qi Liu,Hongbo Zeng
出处
期刊:Journal of Colloid and Interface Science [Elsevier BV]
卷期号:640: 296-308 被引量:19
标识
DOI:10.1016/j.jcis.2023.02.080
摘要

Hypothesis. The removal of stable water-in-oil (W/O) or oil-in-water (O/W) emulsions has been a challenging issue in chemical and oil industry for decades. Traditional demulsifiers were generally designed specifically for treating either W/O or O/W emulsions. A demulsifier that is effective for treating both types of emulsions will be highly desired. Experiments. Novel polymer nanoparticles (PBM@PDM) was synthesized as a demulsifier for treating both W/O and O/W emulsions prepared by toluene, water, and asphaltenes. The morphology and chemical composition of synthesized PBM@PDM were characterized. Demulsification performance and interaction mechanisms including interfacial tension, interfacial pressure, surface charge properties and surface forces were systematically studied. Findings. PBM@PDM could immediately prompt the coalescence of water droplets upon addition and effectively release the water in asphaltenes-stabilized W/O emulsion. In addition, PBM@PDM successfully destabilized asphaltenes-stabilized O/W emulsion. Not only could PBM@PDM substitute the asphaltenes adsorbed at the water-toluene interface, but they could also dominate the water-toluene interfacial pressure in competition with asphaltenes. The steric repulsion between interfacial asphaltene films could be suppressed in the presence of PBM@PDM. Surface charges significantly influenced the stability of asphaltenes-stabilized O/W emulsion. This work provides useful insights into the interaction mechanisms of asphaltene-stabilized W/O and O/W emulsions.
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