Ochoa Chrystian, Xu Chenxian, Martínez Narváez Carina D V, Yang William, Zhang Yiran, Sharma Vivek
Department of Chemical Engineering, University of Illinois at Chicago, Chicago, IL, USA.
Soft Matter. 2021 Oct 13;17(39):8915-8924. doi: 10.1039/d1sm01169c.
Sodium naphthenates (NaNs), found in crude oils and oil sands process-affected water (OSPW), can act as surfactants and stabilize undesirable foams and emulsions. Despite the critical impact of soap-like NaNs on the formation, properties, and stability of petroleum and OSPW foams, there is a significant lack of studies that characterize foam film drainage, motivating this study. Here, we contrast the drainage of aqueous foam films formulated with NaN with foams containing sodium dodecyl sulfate (SDS), a well-studied surfactant system, in the relatively low concentration regime (/CMC < 12.5). The foam films exhibit drainage stratification, displaying step-wise thinning and coexisting thick-thin regions manifested as distinct shades of gray in reflected light microscopy due to thickness-dependent interference intensity. Using IDIOM (interferometry digital imaging optical microscopy) protocols that we developed, we analyze pixel-wise intensity to obtain thickness maps with high spatiotemporal resolution (thickness <1 nm, lateral ∼500 nm, time ∼10 ms). The analysis of interference intensity variations over time reveals that the aqueous foam films of both SDS and NaN possess an evolving, dynamic, and rich nanoscopic topography. The nanoscopic thickness transitions for stratifying SDS foam films are attributed to the role played by damped supramolecular oscillatory structural disjoining pressure contributed by the confinement-induced layering of spherical micelles. In comparison with SDS, we find smaller concentration-dependent step size and terminal film thickness values for NaN, implying weaker intermicellar interactions and oscillatory structural disjoining pressure with shorter decay length and periodicity.
环烷酸钠(NaNs)存在于原油和油砂加工影响水(OSPW)中,可作为表面活性剂,稳定不良泡沫和乳液。尽管类似肥皂的NaNs对石油和OSPW泡沫的形成、性质和稳定性有至关重要的影响,但目前严重缺乏对泡沫膜排水特性的研究,这激发了本研究。在这里,我们对比了在相对低浓度范围(/CMC < 12.5)下,用NaN配制的水基泡沫膜与含有十二烷基硫酸钠(SDS,一种研究充分的表面活性剂体系)的泡沫的排水情况。泡沫膜呈现出排水分层现象,表现为逐步变薄以及厚 - 薄区域共存,在反射光显微镜下由于厚度依赖的干涉强度而呈现出不同深浅的灰色阴影。使用我们开发的IDIOM(干涉数字成像光学显微镜)协议,我们分析逐像素强度以获得具有高时空分辨率的厚度图(厚度 < 1 nm,横向 ∼500 nm,时间 ∼10 ms)。对干涉强度随时间变化的分析表明,SDS和NaN的水基泡沫膜都具有不断演变、动态且丰富的纳米级形貌。分层SDS泡沫膜的纳米级厚度转变归因于球形胶束的受限诱导分层所贡献的阻尼超分子振荡结构分离压力所起的作用。与SDS相比,我们发现NaN的浓度依赖性步长和最终膜厚度值更小,这意味着胶束间相互作用和振荡结构分离压力较弱,衰减长度和周期更短。