Electroosmotically enhanced mass transfer through polyacrylamide gels

• Published in: Journal of colloid and interface science 2006-08, Vol.300 (1), p.429-436
• Main Authors: Matos, Marvi A., White, Lee R., Tilton, Robert D.
• Format: Article
• Language: English
• Subjects: Acrylic Resins - chemistry; Biosensing Techniques; Crosslinked gels; Electrochemistry; Electroosmosis; Flux enhancement; Gels - chemistry; Hydrogel; Mass transport; Nanoparticles; Osmosis; Particle immobilization; Polyacrylamide; Silica
• ISSN: 0021-9797; 1095-7103
• DOI: 10.1016/j.jcis.2006.03.036

We present an internal pumping strategy to enhance solute fluxes in polymer gels. The method is based on electroosmotic flow driven by an electric field applied across a gel that has been doped with charged colloidal inclusions. This work is motivated by the need to enhance the transport in gel-based biosensor devices whose response dynamics are often mass transfer limited. In this case, polyacrylamide gel slabs were doped with immobilized, charged silica colloids, and the flux of a fluorescent tracer was measured as a function of applied field strength, the volume fraction and size of the colloidal silica inclusions, and the bulk electrolyte composition. Significant flux enhancements were achieved with applied electric currents on the order of a few mA. Control experiments indicated that the flux enhancement was not due to any distortion of the gel diffusional properties in response to the presence of the inclusions. At a constant inclusion volume fraction, the electroosmotic solute flux enhancement was strongest for the smallest particle sizes that provide the highest total surface area, consistent with the electroosmotic mechanism whereby fluid flow is generated along the solid/liquid interface. Electroosmotic convection pumped by charged silica nanoparticle inclusions is demonstrated as a means to enhance mass transport through crosslinked polyacrylamide gels.