FACTORS INFLUENCING THE FLOCCULATION OF COLLOIDAL PARTICLES BY A MODEL ANIONIC POLYELECTROLYTE

Citation
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
Citations number
34
Categorie Soggetti
Chemistry Physical
ISSN journal
09277757
Volume
119
Issue
2-3
Year of publication
1996
Pages
229 - 239
Database
ISI
SICI code
0927-7757(1996)119:2-3<229:FITFOC>2.0.ZU;2-7
Abstract
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.