Single-layer graphene oxide sheets are interesting as a flexible 2D material, with xy-dimensions variable up to a centimetre in length and a z-thickness of a single carbon atom. The presence of oxygen atoms with functional groups, such as hydroxy, epoxy, carboxylic acid, ketone, or aldehyde, provides graphene oxide (GO) with polarity. This unique property allows GO to disperse as single sheets in polar solvents like water or DMSO at low concentrations, in the absence of electrolytes or other colloidal particles.
What happens to particle size distributions when making reactive surfactants and polymer colloids by emulsion polymerization?
When we synthesize polymer colloids by emulsion polymerization, molecular surfactants are often employed. These are required to keep the polymer latex particles dispersed in the water phase, so that they do not clump together, a phenomenon known as coagulation. Keeping polymer dispersions stable is especially important in end applications, such as waterborne coatings and adhesives.
A downside of the use of surfactant molecules is that they can desorb from the surface of the latex particles. This makes the particles colloidally unstable, and they coagulate. This can be disastrous in product formulations, such as water-based paints which have many components. Another downside of this mobility of the surfactant molecules is that they can migrate in the final coating, once applied on a substrate. This leads to deterioration of the properties of the coated film.
Innovation in Emulsion Polymerization process opens window to Janus and patchy particles
Emulsion polymerization is of pivotal importance as a route to the fabrication of water-based synthetic polymer colloids. The product is often referred to as a polymer latex and plays a crucial role in a wide variety of applications spanning coatings (protective/decorative/automotive), adhesives (pressure sensitive/laminating/construction), paper and inks, gloves and condoms, carpets, non-wovens, leather, asphalt paving, redispersible powders, and as plastic material modifiers.
Since its discovery in the 1920s the emulsion polymerization process and its mechanistic understanding has evolved. Our most noticeable past contributions include the first reversible-deactivation nitroxide-mediated radical emulsion polymerization (Macromolecules 1997: DOI 10.1021/ma961003s), and the development and mechanistic understanding of Pickering mini-emulsion (Macromolecules 2005: DOI 10.1021/ma051070z) and emulsion polymerization processes (J. Am. Chem. Soc. 2008: DOI 10.1021/ja807242k). The latest on nano-silica stabilized Pickering Emulsion Polymerization from our lab can be found here.
One quest in emulsion polymerization technology that remains challenging and intriguing is control of the particle morphology. It is of importance as the architecture of the polymer colloid influences its behavioural properties when used in applications. We now report in ACS Nano an elegant innovation in the emulsion polymerization process which makes use of nanogels as stabilizers and allows us to fabricate Janus and patchy polymer colloids.