Urm. Kjellin et al., INTERACTIONS BETWEEN ADSORBED LAYERS OF A LOW CHARGE-DENSITY CATIONICPOLYELECTROLYTE ON MICA IN THE ABSENCE AND PRESENCE OF ANIONIC SURFACTANT, Journal of colloid and interface science, 190(2), 1997, pp. 476-484
Interactions between two negatively charged mica surfaces across aqueo
us solutions containing various amounts of a 10% charged cationic poly
electrolyte have been studied, It is found that the mica surface charg
e is neutralized when the polyelectrolyte is adsorbed from a 10-50 ppm
aqueous solution. Consequently no electrostatic double-layer force is
observed. Instead an attractive force acts between the surfaces in th
e distance regime 250-100 Angstrom. We suggest that this attraction is
caused by bridging. Additional adsorption takes place when the polyel
ectrolyte concentration is increased to 100 and 300 ppm, and a long-ra
nge repulsion develops. This repulsive force is both of electrostatic
and steric origin. The polyelectrolyte layer adsorbed from a 50 ppm so
lution does not desorb when the polyelectrolyte solution is replaced w
ith an aqueous polyelectrolyte-free solution. Injection of sodium dode
cyl sulfate (SDS) into the measuring chamber to a concentration of abo
ut 0.01 CMC (8.3 x 10(-5) M) does not affect the adsorbed layers or th
e interaction forces. However, when the SDS concentration is increased
to 0.02 CMC (0.166 mM) the adsorbed layer expands dramatically due to
adsorption of SDS to the polyelectrolyte chains. The sudden swelling
suggests a cooperative adsorption of SDS to the preadsorbed polyelectr
olyte layer and that the critical aggregation concentration between th
e polyelectrolyte and SDS at the surface is about 0.02 CMC. The floccu
lation behavior of the polyelectrolyte in solution upon addition of SD
S was also examined. It was found that 0.16-0.32 mol SDS/mol charged s
egments on the polyelectrolyte is enough to make the solution slightly
turbid. (C) 1997 Academic Press.