Martin Hazel P, Brooks Nicholas J, Seddon John M, Luckham Paul F, Terrill Nick J, Kowalski Adam J, Cabral João T
Department of Chemical Engineering, Imperial College London, London SW7 2AZ, UK.
Soft Matter. 2016 Feb 14;12(6):1750-8. doi: 10.1039/c5sm02689j. Epub 2016 Jan 7.
We investigate the effect of microfluidic flow on the microstructure and dynamics of a model surfactant mixture, combining synchrotron Small Angle X-ray Scattering (SAXS), microscopy and rheology. A system comprising a single-chain cationic surfactant, hexadecyl trimethyl ammonium chloride (C16TAC), a short-chain alcohol (1-pentanol) and water was selected for the study due to its flow responsiveness and industrial relevance. Model flow fields, including sequential contraction-expansion (extensional) and rotational flows, were investigated and the fluid response in terms of the lamellar d-spacing, orientation and birefringence was monitored in situ, as well as the recovery processes after cessation of flow. Extensional flows are found to result in considerable d-spacing increase (from approx 59 Å to 65 Å). However, under continuous flow, swelling decreases with increasing flow velocity, eventually approaching the equilibrium values at velocities ≃2 cm s(-1). Through individual constrictions we observe the alignment of lamellae along the flow velocity, accompanied by increasing birefringence, followed by an orientation flip whereby lamellae exit perpendicularly to the flow direction. The resulting microstructures are mapped quantitatively onto the flow field in 2D with 200 μm spatial resolution. Rotational flows alone do not result in appreciable changes in lamellar spacing and flow type and magnitude evidently impact the fluid microstructure under flow, as well as upon relaxation. The findings are correlated with rheological properties measured ex situ to provide a mechanistic understanding of the effect of flow imposed by tubular processing units in the phase behavior and performance of a model surfactant system with ubiquitous applications in personal care and coating industries.
我们结合同步加速器小角X射线散射(SAXS)、显微镜和流变学,研究了微流体流动对模型表面活性剂混合物微观结构和动力学的影响。由于其流动响应性和工业相关性,选择了一个由单链阳离子表面活性剂十六烷基三甲基氯化铵(C16TAC)、短链醇(1-戊醇)和水组成的体系进行研究。研究了包括顺序收缩-膨胀(拉伸)和旋转流动在内的模型流场,并原位监测了层状d间距、取向和双折射方面的流体响应,以及流动停止后的恢复过程。发现拉伸流动会导致d间距显著增加(从约59 Å增加到65 Å)。然而,在连续流动下,溶胀随着流速的增加而减小,最终在流速≃2 cm s(-1)时接近平衡值。通过单个收缩处,我们观察到片层沿流速方向排列,同时双折射增加,随后发生取向翻转,即片层垂直于流动方向离开。由此产生的微观结构以200 μm的空间分辨率在二维流场中进行了定量映射。仅旋转流动不会导致层状间距有明显变化,并且流动类型和大小显然会影响流动状态下以及松弛时的流体微观结构。这些发现与非原位测量的流变学性质相关联,以提供对管式加工单元施加的流动在模型表面活性剂体系的相行为和性能中的影响的机理理解,该体系在个人护理和涂料行业有广泛应用。