Encapsulation of inorganic particles via miniemulsion polymerization

• Published in: Macromolecular symposia. Vol. 155; no. 1; pp. 181 - 198
• Main Authors: Erdem, Bedri, Sudol, E. David, Dimonie, Victoria L., El-Aasser, Mohamed S.
• Format: Journal Article
• Language: English
• Published: Weinheim WILEY-VCH Verlag 01.04.2000; WILEY‐VCH Verlag
• Subjects: Dispersions; Droplets; Encapsulation; Monomers; Polymerization; Stability; Surface chemistry; Titanium dioxide
• ISSN: 1022-1360; 1521-3900
• DOI: 10.1002/1521-3900(200004)155:1<181::AID-MASY181>3.0.CO;2-2

The encapsulation of TiO2 particles via miniemulsion polymerization is strongly dependent on the size and stability of the inorganic particles in the monomer medium in which they are initially dispersed. It was found from XPS and FT‐IR studies that both the hydrophilic and hydrophobic TiO2 particles, which were studied, have hydroxyl groups present on their surfaces, which can strongly interact with the amine end‐groups of the polymeric stabilizer, OLOA370 (polybutene‐succinimide diethyl triamine). It was found from the dispersion and adsorption studies that the amount of OLOA370 retained on the TiO2 particles is strongly dependent on the area exposed by the sonification that is applied to break up the aggregates in the dispersion process. The TiO2 dispersions in styrene monomer were themselves dispersed as miniemulsion droplets and subsequently polymerized. It was concluded from the density gradient column (DGC) analysis of the latexes obtained from the encapsulation polymerizations, that the stability of the inorganic particles in the monomer, as well as their particle size, significantly influence the encapsulation efficiencies. The use of the hydrophilic titanium dioxide particles in combination with the stabilizer, OLOA370, resulted in a good dispersibility, dispersion stability, and small TiO2 particle size. This lead to better encapsulation efficiencies compared to the hydrophobic particles. The poorer results obtained with the hydrophobic TiO2 particles were attributed to their larger particle size, which resulted from the reduced adsorption of the OLOA370. Fewer hydroxyls and the presence of the trimethoxy octyl silane (TMOS) groups, which themselves are unable to provide sufficient steric stability, are proposed to explain these findings.