Origami, the art of paper folding, has recently seen an upsurge of interest due to its use in guiding the design of lightweight deployable structures. Despite the heavy use of thin films in origami designs, comprehensive mechanical understanding lags behind. This is partly because origami structures are often made from new materials for which bulk material properties are not available. In this work, we show how bending can be used to gather broad mechanical information from thin films, and we show how that information can be applied to more complex structures. Explicitly, we use the technique to measure the Young's modulus and monitor the force recovery of polydimethylsiloxane, polystyrene, and polycarbonate films. Our force recovery data are consistent with the sparse published data available but reveal a previously unreported film thickness dependence. We hypothesize that the thickness dependence is related to the strain gradient present in bending.

Polymer covered emulsion droplets have a considerable number of applications ranging from active cosmetics to advance drug delivery systems. In many of these systems the emulsion droplets do not exist in isolation but interact with other drops, surfaces and particles. In a step towards understanding how these complex mechanical interactions take place, we examine the interaction between a block copolymer covered emulsion droplet (polystyrene-b-poly(ethylene oxide) (PS-PEO) covered toluene) and a flat mica interface. As buoyancy pushes the droplet upwards, it buckles in as it nears the mica and traps a droplet of the surrounding fluid. The trapped outer fluid (water/glycerine in our experiment) drains out through an annular region of PEO brush. This study focuses on the late stage drainage, unique to large molecule surfactants, and examines the effects of the polymer and droplet size on the drainage rate. We introduce a scaling model of the drainage which highlights the importance of three lengthscales in the problem - the brush height, the slip length along the emulsion drop interface and the width of the annular contact region.

There is considerable interest in the fabrication and mechanics of soft spheres and capsules because of their use in a large number of applications ranging from targeted drug delivery to cosmetically active agents. Many systems, such as lipid and block copolymer vesicles, are already finding considerable industrial use where the performance of soft spheres depends intimately on their mechanics. New advanced features such as fast cargo delivery can be realized only if they fit into the existing mechanical niche of the system in question. Here we present a model system to demonstrate how a capsule structure can be fundamentally changed while maintaining its overall mechanical response as well as a simple, universal method to measure the resulting capsule material properties. Specifically, we use confocal microscopy to adapt the sessile drop geometry to a measurement of the static properties of an ensemble of polystyrene-b-poly(ethylene oxide) (PS-PEO)-stabilized oil droplets. We then synthesize a polystyrene-b-poly(acrylic acid)-b-polystyrene (PS-PAA-PS) elastic-shell-coated emulsion drop that shows an identical deformation to the fluidlike PS-PEO droplets. Both systems, in sessile geometry, can be related to their basic material properties through appropriate modeling. We find that the elastic shell is dominated by its surface tension, easily enabling it to match the static response of a purely fluid drop.

Abstract:Polymer stabilized emulsions are commonplace in industries ranging from cosmetics and foods to pharmaceuticals. Understanding the physical properties of emulsions is of critical importance to the rapid advancement of industrial applications. In this work, we use a sessile drop geometry to examine the effects of viscosity changes of the surrounding glycerine/water solution on polystyrene-b-polyethylene oxide (PS-PEO) covered toluene droplets. In the experiment, emulsion drops are driven by the buoyant force into a smooth mica surface. The drops buckle as they approach the mica, trapping some of the outer fluid which slowly drains out over time. The characteristic time of the drainage process as well as the surface tension was measured as a function of glycerine/water concentration. The surface tension is found to have a minimum at a glycerine concentration of approximately 50% (by weight to water) and the drainage rate is shown to be well described by a recent model. The simple experiment not only shows how critical features of emulsion stability can be easily and reliably measured, but also identifies important new features of the drainage process.