Hw. Walker et Sb. Grant, FACTORS INFLUENCING THE FLOCCULATION OF COLLOIDAL PARTICLES BY A MODEL ANIONIC POLYELECTROLYTE, Colloids and surfaces. A, Physicochemical and engineering aspects, 119(2-3), 1996, pp. 229-239
The flocculation of charged colloidal particles by oppositely charged
polyelectrolytes is investigated, using as a model system, positively
charged latex microspheres and negatively charged single-stranded DNA
of varying chain length from 3-mers up through 1400-mers. For DNA mole
cules with chain lengths of eight or more monomers there is a single p
olymer mass (0.1 mu g ml(-1)) which neutralizes the particle surface c
harge and destabilizes the particle suspension in the presence of 0.00
5 hi NaCl at a particle concentration of 1.47 x 10(10) particles per m
i. The coagulation kinetics at this optimum polymer dose are diffusion
-limited, even for the largest polymer tested. Hence, the electrostati
c ''patch'' model for the flocculation of negatively charged particles
by cationic polymers proposed by Gregory (Gregory, J. Colloid Interfa
ce Sci., 42 (1973) 448; 55 (1976) 35) does not apply to our system. Th
e mechanism responsible for polymer flocculation in a given system app
ears to depend upon the relative spacing of charged groups on the poly
mer backbone and particle surface, the size and inherent flexibility o
f the polymer in question, and the nature of the initial polymer-parti
cle interaction.