Synthesis of Nonspherical Colloidal Particles with Anisotropic Properties
Original Entry by Ryan Truby
AP 225 - Introduction to Soft Matter
November 28, 2012
Authors: J.-W. Kim, R. J. Larsen, D. A. Weitz
Citation: J.-W. Kim, R. J. Larsen, and D. A. Weitz. Synthesis of Nonspherical Colloidal Particles with Anisotropic Properties. JACS. 2006, 128, 14374-14377.
Related Course Keywords: adsorption, surfactants
Background and Introduction
Microscale colloids with anisotropic morphologies have proven useful to the development of novel materials and fluids for optical, biomedical, and self-assembly applications. At Harvard University, researchers in Professor Weitz's research group are bestowing anisotropic colloids with Janus-like chemical functionalities to create "colloidal surfactants."
A brief summary of the article cited above is presented along with some demonstrations of the surfactant-like properties of the anisotropic colloids developed by in Professor Weitz's lab.
The authors synthesized anisotropic microparticles with dumbbell morphologies that were composed of (or combinations of) polystyrene (PS), polymethyl methacrylate (PMMA), and polybutyl methacrylate (PBMA). The cross-linked PS regions of the anisotropic colloids could be surface functionalized after synthesis with glycidyl methacrylate (GMA), 9-vinylanthracene, and vinylsilane. The synthesis scheme for the colloids' synthesis is given in Figure 1.
Briefly, following a previously reported protocol, spherical, cross-linked PS microparticles were synthesized and swollen for 10 hours to a diameter of approximately 2.7 microns in a solution containing MMA/BMA/styrene monomer (20 vol %), divinylbenzene (DVB, 1 vol %), and the azo polymerization initiator V-65B (2,2'-azodi(2,4'-dimethylvaleronitrile)) at room temperature. The monomer-loaded PS beads were then polymerized at 70 degrees Celsius for 8 hours. During this polymerization step, elastic stress in the swollen PS microparticle drives a phase separation between the PS of the initial spherical particle and the monomer within: a new bulb of monomer nucleates on the surface of the PS particle, initiating the formation of a newly formed polymer bulb. When the initiator is present, nearly all available monomers in solution polymerize at this new bulb. The polymer within the PS particles breach the PS particles' surfaces at one favorable location (i.e. a route of lease resistance) because this phase separation is stress-driven (and in the case of MMA/BMA, the growing polymer is not miscible with PS), resulting in anisotropic colloidal particles with only two bulbs. At the end of the 8-hour polymerization period, the anisotropic colloidal particles are rigid, with one bulb containing mostly PS and the other containing mostly polymer of the previously added monomer.
When styrene monomer was used, the authors created a PS dumbbell. By initially functionalizing the cross-linked PS particle with GMA, this all-PS dumbbell had one surface-functionalized, cross-linked PS bulb and one "bare" PS bulb. The authors were able to make the GMA-functionalized bulb hydrophilic by binding hydrophilic poly(ethylene iminie) polymer chains (MW = 8 kDa) to the free GMA groups. The resulting anisotropic PS particle was effectively amphiphillic.
The size and geometries of the bulbs of the anisotropic colloids could be tuned by altering the concentration of monomer added to the cross-linked PS microparticles...
Discussion and Relevance to Soft Matter
 J.-W. Kim, R. J. Larsen, and D. A. Weitz. Synthesis of Nonspherical Colloidal Particles with Anisotropic Properties. JACS. 2006, 128, 14374-14377.
 J.-W. Kim, D. Lee, H. C. Shum, and D. A. Weitz. Colloid Surfactants for Emulsion Stabilization. Adv. Mater. 2008, 20, 3239-3243.