Transport dynamics of charged colloidal particles during directional drying of suspensions in a confined microchannel

Directional drying of colloidal suspensions, experimentally observed to exhibit mechanical instabilities, is a nonequilibrium procedure that is susceptible to geometric confinement and the properties of colloidal particles. Here, we develop an advection-diffusion model to characterize the transport dynamics for unidirectional drying of a suspension consisting of charged particles in a confined Hele-Shaw cell. We consider the electrostatic interactions by means of the Poisson-Boltzmann cell approach with the viscous flow confined to the cell. By solving the nonequilibrium transport equations, we clarify how the multiple parameters, such as drying rate, confinement ratio, and the monovalent slat concentration, affect the transport dynamics of charged colloidal particles. We find that the drying front recedes into the cell with linear behavior, while the liquid-solid transition front recedes with power law behaviors. The faster evaporation rate creates a rapid formation of the drying front and produces a thinner transition layer. We show that confinement is equivalent to raising the effective concentration in the cell, and, accordingly, the drying front appears earlier and grows more rapidly. Under geometric confinement, a longer fully dried film is created while the total drying time is shortened. Moreover, we have theoretically illustrated that low salt loadings cause a large collective diffusivity of charged colloidal particles, which results in a colloidal network by aggregation. Thus, the drying behavior alters dramatically as salt loadings decrease, since the resulting compacted clusters of charged particles eventually convert the suspension into a gel-like material instead of a simple fluid. Our model is consistent with the current experiments and provides a simple insight for applications in directional solidification and microfluidics.