The kinetics of poly(N-isopropylacrylamide) microgel latex formation

Abstract

Conversion versus time curves were measured for poly(N-isopropylacrylamide) microgel latexes prepared by polymerization in water with sodium dodecyl sulfate, SDS. Polymerization rates increased with temperature with methylenebisacrylamide crosslinking monomer consumed faster thanN-isopropylacrylamide. The particle diameter decreased with increasing concentrations of SDS in the polymerization recipe and there was evidence that the rate of polymerization increased somewhat with SDS concentration. Particle formation occurred by homogeneous nucleation as micelles were absent.

Comparison of particle size distributions from dynamic light scattering to those from a centrifugal sizer led to the conclusion that larger particles within a specific latex were less swollen with acetonitrile than were the smaller ones. This was interpreted as evidence for the polymer in larger particles having a higher crosslink density. Particle swelling was estimated from swelling ratios defined as the particle volume at 25 °C divided by the volume at 50 °C. In the absence of crosslinking poly(N-isopropylacrylamide) linear chains would disolve at 25 °C. The swelling results indicated that the average crosslink density in the particles decreased with conversion. This was explained by the observation that the methylenebisacrylamide was consumed more quickly and is typical of crosslinking in emulsion polymerization where polymer particles have high polymer concentrations at their birth.