Spatial mapping and scaling of the shear-induced transformation from bicontinuous microemulsions towards lamellar structures by coupling microfluidics and SANS

被引:3
作者
Fischer, Julian [1 ]
Porcar, Lionel [2 ]
Cabral, Joao T. [3 ]
Sottmann, Thomas [1 ]
机构
[1] Univ Stuttgart, Instiute Phys Chem, Pfaffenwaldring 55, D-70569 Stuttgart, Germany
[2] Inst Laue Langevin, 71 Ave Martyrs,CS 20156, F-38042 Grenoble 9, France
[3] Imperial Coll London, Dept Chem Engn, London SW7 2AZ, England
基金
英国工程与自然科学研究理事会;
关键词
AMPHIPHILIC BLOCK-COPOLYMERS; X-RAY-SCATTERING; PHASE-BEHAVIOR; WETTING TRANSITION; CHANNEL FLOWS; SURFACTANT; WATER; MEMBRANES; MICROSTRUCTURE; ORIENTATION;
D O I
10.1039/d3sm00558e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Coupling microfluidics and small-angle neutron scattering (SANS), we investigate the influence of shear flow on a model bicontinuous microemulsion of D2O/n-octane/C10E4, examining the role of membrane volume fraction in the transformation towards a lamellar structure. We employ a contraction-expansion geometry with flow velocities in excess of 10 m s(-1) and spatially map the microfluidic field using a small SANS beam, illuminating down to 10 nL sample volumes. The shear-induced, progressive, bicontinuous-to-lamellar transition is found to be promoted by additional extensional flow (>10(3) s(-1)), while fast relaxation kinetics (<2 ms) return the scattering pattern to isotropic shortly after the constriction. Further, increasing the domain size of the bicontinuous structure (determined by the membrane volume fraction) appears to amplify its response to shear. Hence, the structural changes within the dilute bicontinuous microemulsions simply scale with the volume fraction of the membrane. By contrast, the stronger response of the microemulsion with the smallest domain size, located near the bicontinuous/lamellar coexistence, indicates an influence of an already more ordered structure with fewer passages. Our findings provide insight into the high shear behaviour of microemulsions of both academic and industrial relevance.
引用
收藏
页码:7070 / 7083
页数:15
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