Scientific article
English

Charging and aggregation of positively charged latex particles in the presence of anionic polyelectrolytes

Published in

The journal of physical chemistry. B, vol. 111, no. 29, p. 8626-8633

Publication date

2007

Abstract

Charging behavior and colloidal stability of amidine latex particles are studied in the presence of poly(sodium styrene sulfonate) (PSS) and KCl. Detailed measurements of electrophoretic mobility, adsorbed layer thickness, and aggregation (or coagulation) rate constant on varying the polymer dose, molecular mass of the polymer, and ionic strength are reported. Polyelectrolyte adsorption leads to the characteristic charge reversal (or overcharging) of the colloidal particles at the isoelectric point (IEP). In accordance with classical Derjaguin-Landau-Verwey-Overbeek (DLVO) theory, uncharged particles tend to aggregate because of van der Waals attraction, whereas charged particles are stabilized by electrical double layer repulsion. Attractive patch-charge interactions originating from the laterally inhomogeneous structure of the adsorbed polymer substantially decrease the suspension stability or even accelerate the aggregation rate beyond diffusion control. These electrostatic non-DLVO forces become progressively important with increasing molecular mass of the polymer and the ionic strength of the solution. At higher polymer dose of typically 10 times the IEP, one observes the formation of a saturated layer of the adsorbed polymer with a thickness of several nanometers. Its thickness increases with increasing molecular mass, whereby the layer becomes increasingly porous. This layer does not seem to be involved in the suspension stabilization, since at such high polymer doses the double layer repulsion has attained sufficient strength to stabilize the suspension.

Citation (ISO format)

GILLIES, Graeme, LIN, Wei, BORKOVEC, Michal. Charging and aggregation of positively charged latex particles in the presence of anionic polyelectrolytes. In: The journal of physical chemistry. B, 2007, vol. 111, n° 29, p. 8626–8633. doi: 10.1021/jp069009z

Main files (1)

Article (Published version)

Identifiers

Journal ISSN

1520-5207
628views
1downloads

Technical informations

Creation

06/01/2011 11:01:00

First validation

06/01/2011 11:01:00

Update

14/03/2023 16:11:20

Status update

14/03/2023 16:11:20

Last indexation

29/10/2024 17:40:47
All rights reserved by Archive ouverte UNIGE and the University of Geneva
OpenAIRE Indexed & Validated