The well-known phenomenon of partitioning of bioparticles in two-phase
aqueous polymeric systems is extended to a variety of polymer (acryli
c latex) and inorganic (TiO2) colloidal particles. It is demonstrated
that particle partitioning into a particular phase is controlled in ra
tional ways by particle surface chemistry, vie., hydrophobicity, funct
ional groups such as hydroxyl and carboxyl, and pH effects, in relatio
n to the chemical nature of the water soluble polymers (WSPs) that com
prise the phase-separated system. WSPs include poly(ethylene oxide), p
oly(N-vinylpyrrolidone), dextran, and a hydrophobe-terminated water so
luble polyurethane based on polyethylene oxide. Mixtures of colloidal
particles can be separated by selective partitioning.