期刊
ACS NANO
卷 12, 期 2, 页码 1050-1061出版社
AMER CHEMICAL SOC
DOI: 10.1021/acsnano.7b05391
关键词
micelles; foams; thin films; disjoining pressure; imaging; DLVO theory; surface forces
类别
资金
- College of Engineering at University of Illinois at Chicago
- Campus Research Board
- Department of Chemical Engineering at University of Illinois at Chicago
Freestanding films of soft matter containing micelles, nanoparticles, polyelectrolyte-surfactant complexes, bilayers, and smectic liquid crystals exhibit stratification. Stepwise thinning and coexisting thick-thin regions associated with drainage via stratification are attributed to the confinement-induced structuring and layering of supramolecular structures, which contribute supramolecular oscillatory structural forces. In freestanding micellar films, formed by a solution of an ionic surfactant above its critical micelle concentration, both interfacial adsorption and the micelle size and shape are determined by the concentration of surfactant and of added electrolytes. Although the influence of surfactant concentration on stratification has been investigated before, the influence of added salt, at concentrations typically found in water used on a daily basis, has not been investigated yet. In this contribution, we elucidate how the addition of salt affects stepwise thinning: step size, number of steps, as well as the shape and size of nanoscopic nonflat structures such as mesas in micellar foam films formed with aqueous solutions of anionic surfactant (sodium dodecyl sulfate (SDS)). The nanoscopic thickness variations and transitions are visualized and analyzed using IDIOM (Interferometry Digital Imaging Optical Microscopy) protocols with exquisite spatiotemporal resolution (thickness similar to 1 nm, time <1 ms). In contrast to nanoparticle dispersions that show no influence of salt on step size, we find that the addition of salt to micellar freestanding films results in a decrease in step size as well as the number of stepwise transitions, in addition to changes in nucleation and growth of mesas, all driven by the corresponding change in supramolecular oscillatory structural forces.
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