Bachnak Rana, Narayan Shweta, Moravec Davis B, Hauser Brad G, Dallas Andrew J, Dutcher Cari S
Department of Mechanical Engineering, University of Minnesota─Twin Cities, Minneapolis, Minnesota 55455, United States.
Donaldson Company, Bloomington, Minnesota 55431, United States.
J Phys Chem B. 2024 Nov 7;128(44):10986-10998. doi: 10.1021/acs.jpcb.4c04691. Epub 2024 Oct 24.
Liquid-liquid separation is a critically important process in the treatment of emulsions that can occur in our environment, such as oily stormwater, shipboard bilgewater, or off-shore oil spill treatment. Effective filtration systems, including coalescing filters, are essential for mitigating these environmental pollutants. Achieving this requires a comprehensive understanding of liquid-liquid interface dynamics influenced by additives and surfactants. Furthermore, understanding the impact of surfactants on emulsion stability in saline environments is vital for optimizing filtration processes and ensuring the protection of marine and freshwater ecosystems. In this work, these effects are highlighted using measurements performed across a range of droplet size, surfactant concentration, viscosity ratios, and saline presence. Dynamic IFT measurements are conducted using the pendant drop method for water in light mineral oil, with and without salt in the water phase. The effect of salt addition is also highlighted by using microfluidic coalescence experiments, in which it was found that the addition of salt increases the dimensionless drainage time below the critical micelle concentration. The second focus of this work is to study the effect of bulk phase viscosity on the stability. Dynamic IFT measurements are performed at both millimeter and micrometer scales using pendant drop experiments and microfluidic tensiometry, respectively, involving light and heavy mineral oils with varying SPAN80 surfactant concentrations. The surfactant diffusivity and interfacial adsorption and desorption rates are then extracted by fitting a surfactant diffusion and equation of state equations to the dynamic IFT measurements. The results of the IFT decay, surfactant diffusivity, and adsorption rates are compared at two different viscosity ratios. This study also compares the times required for IFT relaxation with the film drainage times in water-in-oil systems. The comparison aids in comprehending the impact of competing timescales during film drainage. The findings presented in this paper offer valuable insights into the design and optimization of liquid-liquid filtration systems, especially when operating under challenging environmental conditions, such as in saline environments. The principles explored here can be applied to improving industrial water treatment and in the design of advanced filtration technologies for chemical and petrochemical industries, particularly those involving flow, contributing to more sustainable and efficient practices in handling emulsified waste streams.
液-液分离是处理我们环境中可能出现的乳液(如含油雨水、船舶舱底水或海上溢油处理)的一个极其重要的过程。有效的过滤系统,包括聚结过滤器,对于减轻这些环境污染物至关重要。要实现这一点,需要全面了解受添加剂和表面活性剂影响的液-液界面动力学。此外,了解表面活性剂在盐水环境中对乳液稳定性的影响对于优化过滤过程和确保保护海洋和淡水生态系统至关重要。在这项工作中,通过在一系列液滴尺寸、表面活性剂浓度、粘度比和盐水存在情况下进行的测量突出了这些影响。使用悬滴法对轻质矿物油中的水进行动态界面张力(IFT)测量,水相中有无盐。通过微流控聚结实验也突出了加盐的效果,其中发现加盐会增加临界胶束浓度以下的无量纲排水时间。这项工作的第二个重点是研究本体相粘度对稳定性的影响。分别使用悬滴实验和微流控张力测量法在毫米和微米尺度上进行动态IFT测量,涉及不同SPAN80表面活性剂浓度的轻质和重质矿物油。然后通过将表面活性剂扩散和状态方程拟合到动态IFT测量中提取表面活性剂扩散率以及界面吸附和解吸速率。在两种不同的粘度比下比较IFT衰减、表面活性剂扩散率和吸附速率的结果。本研究还比较了IFT松弛所需时间与油包水体系中的液膜排水时间。这种比较有助于理解液膜排水过程中竞争时间尺度的影响。本文提出的研究结果为液-液过滤系统的设计和优化提供了有价值的见解,特别是在具有挑战性的环境条件下运行时,如在盐水环境中。这里探索的原理可应用于改进工业水处理以及化学和石油化工行业先进过滤技术的设计,特别是那些涉及流动的技术,有助于在处理乳化废物流时实现更可持续和高效的实践。