In this article, we present the mobilities of prolate ellipsoidal micrometric particles close to an air–water interface measured by dual wave reflection interference microscopy. Particle's position and orientation with respect to the interface are simultaneously measured as a function of time. From the measured mean square displacement, five particle mobilities (3 translational and 2 rotational) and two translational–rotational cross-correlations are extracted. The fluid dynamics governing equations are solved by the finite element method to numerically evaluate the same mobilities, imposing either slip and no-slip boundary conditions to the flow at the air–water interface. The comparison between experiments and simulations reveals an agreement with no-slip boundary conditions prediction for the translation normal to the interface and the out-of-plane rotation, and with slip ones for parallel translations and in-plane rotation. We rationalize these evidences in the framework of surface incompressibility at the interface.

Liquid mixtures composed of colloidal particles and much smaller non-adsorbing linear homopolymers can undergo a gelation transition due to polymer-mediated depletion forces. We now show that the addition of linear polymers to suspensions of soft colloids having the same hydrodynamic size yields a liquid-to-gel-to-re-entrant liquid transition. In particular, the dynamic state diagram of 1,4-polybutadiene star–linear polymer mixtures was determined with the help of linear viscoelastic and small-angle X-ray scattering experiments. While keeping the star polymers below their nominal overlap concentration, a gel was formed upon increasing the linear polymer content. Further addition of linear chains yielded a re-entrant liquid. This unexpected behavior was rationalized by the interplay of three possible phenomena: (i) depletion interactions, driven by the size disparity between the stars and the polymer length scale which is the mesh size of its entanglement network; (ii) colloidal deswelling due to the increased osmotic pressure exerted onto the stars; and (iii) a concomitant progressive suppression of the depletion efficiency on increasing the polymer concentration due to reduced mesh size, hence a smaller range of attraction. Our results unveil an exciting new way to tailor the flow of soft colloids and highlight a largely unexplored path to engineer soft colloidal mixtures.

Confinement and hydrodynamic interactions often play an important role in the fluctuation dynamics of soft matter systems, which can typically be studied using light scattering techniques. With experimental and theoretical methodologies, I demonstrate here that chirality is an additional critical parameter that leads to diverging decay times and correlation lengths in chiral liquid crystal cells with a fully unwound cholesteric helix. This study combines light scattering measurements made in a tailored microscope geometry and theoretical calculations of the decay dynamics of chiral orientational fluctuations---including hydrodynamics---to establish the existence of two soft chiral modes of fluctuations driving the destabilization of the unwound cholesteric. Despite the achirality of the equilibrium state of unwound cholesterics, this study indicates that chirality hides itself in the orientational fluctuation modes and plays a major role in their dynamics, which can be exploited to locally measure the strength of chirality in frustrated chiral liquid crystal cells.