COMPARATIVE-STUDY ON THE COLLOIDAL STABILITY MECHANISMS OF SULFONATE LATEXES

Citation
Jm. Peula et al., COMPARATIVE-STUDY ON THE COLLOIDAL STABILITY MECHANISMS OF SULFONATE LATEXES, Langmuir, 13(15), 1997, pp. 3938-3943
Citations number
39
Categorie Soggetti
Chemistry Physical
Journal title
ISSN journal
07437463
Volume
13
Issue
15
Year of publication
1997
Pages
3938 - 3943
Database
ISI
SICI code
0743-7463(1997)13:15<3938:COTCSM>2.0.ZU;2-W
Abstract
In this work the colloid stability mechanisms of two sulfonated latexe s prepared by different methods are studied. One of the latexes (JM1) was prepared by surfactant-free emulsion copolymerization of styrene ( St) and sodiun styrene sulfonate (NaSS), while the second latex (SN9) was prepared by a two-stage ''shot-growth'' emulsion polymerization pr ocess using NaSS as ionic comonomer, which is included in a larger pro portion in the second stage. The results are two latexes with nearly t he same particle size but very different surface charge densities and, probably, one of them with a significant highly charged ''hairy'' sur face. The anomalous electrokinetic behavior of the sulfonate polystyre ne latexes was a consequence of their electric double-layer structure, and their high colloidal stability was not explained by the classical DLVO theory. This high colloidal stability could be a consequence of the hairy layer formed during the synthesis method (which includes the use of an ionic comonomer that can act as a polymerizable surfactant) . By including several correction factors in the DLVO theory, such as the Stern layer thickness (ionic size) and the hydrodynamic interactio n, a good correlation can be found between the theory and experimental results: the Hamaker constant value so obtained is equal to the theor etical one. If we try to explain the stability results by an electrost eric mechanism, it is possible to find a set of parameters which provi de critical coagulation concentration (ccc) values which are in accord ance with the experimental one; but, however, some controversies appea r in relation to the values of some of the fitting parameters, because the Hamaker constant value is now lower than the theoretical one and the ions have to be dehydrated. Therefore, for the sulfonate latexes p repared by a ''shot-growth'' process, their high colloidal stability c an be well explained by including some correction factors in the DLVO theory, and the use of a steric mechanism gives lower Hamaker constant values, which could mean that the hairy layer of these latexes does n ot seem to be large enough to produce a clear additional steric stabil ization.