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Published November 28, 2017 | Supplemental Material
Journal Article Open

Microstructures and mechanics in the colloidal film drying process

Abstract

We use Brownian Dynamics (BD) simulations and continuum models to study the microstructures and mechanics in the colloidal film drying process. Colloidal suspensions are compressed between a planar moving interface and a stationary substrate. In the BD simulations, we develop a new Energy Minimization Potential-Free (EMPF) algorithm to enforce the hard-sphere potential in confined systems and to accurately measure the stress profile. The interface moves either at a constant velocity U_w or via a constant imposed normal stress Σ_e. Comparing the interface motions to the particle Brownian motion defines the Péclet numbers Pe_U = U_wa/d_0 and Pe_Σ = Σ_ea^3/k_BT, respectively, where d_0 = k_BT/ζ with k_BT the thermal energy scale, ζ the single-particle resistance, and a the particle radius. With a constant interface velocity, thermodynamics drives the suspension behavior when Pe_U ≪ 1, and homogeneous crystallization appears when the gap spacing between the two boundaries pushes the volume fraction above the equilibrium phase boundary. In contrast, when Pe_U ≫ 1, local epitaxial crystal growth appears adjacent to the moving interface even for large gap sizes. Interestingly, the most amorphous film microstructures are found at moderate Pe_U. The film stress profile develops sharp transitions and becomes step-like with growing Péclet number. With a constant imposed stress, the interface stops moving as the suspension pressure increases and the microstructural and mechanical behaviors are similar to the constant velocity case. Comparison with the simulations shows that the model accurately captures the stress on the moving interface, and quantitatively resolves the local stress and volume fraction distributions for low to moderate Péclet numbers. This work demonstrates the critical role of interface motion on the film microstructures and stresses.

Additional Information

© 2017 The Royal Society of Chemistry. The article was received on 07 Aug 2017, accepted on 13 Oct 2017 and first published on 16 Oct 2017. M. W. gratefully acknowledges supports from the Natural Sciences and Engineering Research Council of Canada (NSERC) by a Postgraduate Scholarship (PGS), and the National Science Foundation (NSF) grant CBET-1337097.

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