Martin Selin, Maret Ickler, Gerardo Campos-Villalobos, Fabrizio Camerin, Nicolas Vogel, Antonio Ciarlo, Giovanni Volpe, and Marcel Rey
Date: 6 August 2025
Time: 4:30 PM – 4:45 PM PDT
Place: Conv. Ctr. Room 3
Colloidal systems are integral to industries such as food and cosmetics, where liquid-liquid interfaces—like oils dispersed in water—are common. Whether colloidal particles adsorb to these interfaces depends on multiple factors such as particle surface chemistry, pH and salinity.
Here, we investigate how core–shell particles breach a liquid-liquid interface by using optical tweezers to gently push the particles into dodecane-water interfaces formed by microbubbles. Our core–shell particles feature a silica core and a PDMAEMA shell and by varying the amount of monomer added during synthesis the size of the shell can be tuned. Using the tweezers we measure the extent of the polymer shell. Importantly, we find that uncoated silica particles do not adsorb in pure water, whereas polymer coated particles absorb rapidly once the polymer layer contacts the interface, also when the core itself remains microns away. The longer the polymer the greater the distance from which the particle absorbs.
We also observe similar adsorption other polymer shells like PNIPAM and PVP, indicating that the presence of a polymer coating, rather than its specific chemical composition, is the key factor governing adsorption. At low and high pH the polymer shell contracts, also the binding energy becomes weaker making the absorption slower. In very acidic conditions the binding is so weak that the optical tweezers can pull particles out from the interface, allowing us to directly observe individual polymers detaching. These findings provide new insight into how polymer coatings dictate particle-interface interactions, paving the way for improved control of colloidal behavior.