Role of polyelectrolyte charge density in tuning colloidal forces

Thomas Abraham, D. Christendat, Z. Xu, J. Masliyah, J. F. Gohy, R. Jérôme

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Abstract

An atomic force microscope was used to study the effects of polymer charge density on surface interactions between similarly charged silica surfaces. Copolymers of acrylamide and acrylic acid of three different charge densities (fp = 15, 40, and 70%) were used. The dynamic light-scattering technique was used to obtain the characteristic size of these polymers in solution. Flocculation tests were performed to complement force-distance measurement. At 20 mM KCl and pH ∼ 8.0, the low charge density copolymer (fp = 15%) caused a purely repulsive force profile between silica surfaces irrespective of the added polymer concentration, suggesting a strong adsorption of the copolymer on the surface. The medium (fp = 40%) and high (fp = 70%) charge density copolymers, on the other hand, provided an adhesive bridging attraction at low polymer concentrations, but a purely repulsive force at higher polymer concentrations. The range of these repulsive forces, however, was significantly smaller than that measured for the low charge density polymer. The medium and high charge densities exhibit nearly an identical behavior in controlling the intersurface forces, although the forces are different with respect to magnitude. The flocculation tests follow the same trend as that of force-distance data, where a complete, a partial, and no flocculation observed with high, medium, and low charge density polymers, respectively. In all the cases, the range of surface interactions can be correlated with the polymer chain dimension corresponding to the fast diffusion process (individual chains) obtained from dynamic light-scattering measurements. Mean-field models proposed for charged polymers can qualitatively explain both the dependency of bridging interactions on polymer charge density and the dependency of force-distance profiles on added polymer concentrations. Finally, a mean-field model was quantitively to account for the measured electrosteric interactions and their dependency on polymer charge density.

Original languageEnglish (US)
Pages (from-to)2613-2626
Number of pages14
JournalAICHE Journal
Volume50
Issue number10
DOIs
Publication statusPublished - Oct 1 2004

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All Science Journal Classification (ASJC) codes

  • Biotechnology
  • Environmental Engineering
  • Chemical Engineering(all)

Cite this

Abraham, T., Christendat, D., Xu, Z., Masliyah, J., Gohy, J. F., & Jérôme, R. (2004). Role of polyelectrolyte charge density in tuning colloidal forces. AICHE Journal, 50(10), 2613-2626. https://doi.org/10.1002/aic.10255