Nanolatex Synthesis and CharacterizationOur nanolatexes were prepared via microemulsion polymerization, a special type of dispersion polymerization, from aqueous acrylate/methacrylate microemulsions stabilized by reactive ionic liquid surfactants. To exemplify our process we used methylmethacrylate (MMA) as a comonomer along with the ionic liquid reactive acrylate surfactant 1-(11acryloyloxyundecyl)-3-methylimidazolium bromide (ILBr) to compose the nanolatex precursor solution (microemulsion). ILBr was prepared as described in Refs. 11, 17, and 26 of the main text. This monomer contains an approximately 1% cross-linker, 1,3-bis(11acryloyloxyundecyl)imidazolium bromide as a preparative impurity from alkyl group scrambling in the quaternization step. Ionic liquids are defined as salts, mostly organic, that melt below 100°C; ILBr melts at about 50°C.
Microemulsion PolymerizationA partial ternary phase diagram of this system is illustrated in Fig. S1, where one of the compositions for microemulsion polymerization we utilized is indicated by the "✕" in the lower left corner. The microemulsion domain is a thermodynamically stable and somewhat exotic single phase solution. In the illustrated domain, MMA swollen micelles of ILBr are the most prevalent complexes, although irregular bicontinuous microstructure exists at higher surfactant levels.The latexes were prepared by diluting a stock solution of 60% ILBr (w/w) in MMA with the appropriate amounts of water to reach a total volume of 25 ml for each composition. AIBN initiator was present in the MMA stock solution at 0.5% (w/w) with respect to total monomer weight. The clear microemulsion solutions were then heated overnight at 60 °C in a temperature controlled bath.The compositions ranging from 2 -4% ILBr content showed an increasing presence of a light blue Tyndall haze. This increasing blue haze indicated particles were present and that a dispersion had formed. Another indicator of particle formation was the increasing suspension viscosity with increasing ILBr/MMA content.Portions of each sample were dialyzed against daily changes of deionized water for three days in order to remove unreacted monomer. Dialysis was performed by placing approximately 1.5 ml of latex sample inside a 7 cm piece of regenerated cellulose dialysis