Synergistic Stabilization of Emulsions by a Mixture of Surface-Active Nanoparticles and Surfactant

Bernard P. Binks* and Alexandre Desforges
Surfactant and Colloid Group, Department of Chemistry, University of Hull, Hull HU6 7RX, U.K.
Daniel G. Duff
PT-PDSP, Bayer Technology Services GmbH, 51368 Leverkusen, Germany
Langmuir, 2007, 23 (3), pp 1098–1106
DOI: 10.1021/la062510y
Publication Date (Web): December 6, 2006
Copyright © 2007 American Chemical Society
*

 To whom correspondence should be addressed. E-mail:  b.p.binks@ hull.ac.uk.

Abstract

Abstract Image

The stability and rheology of tricaprylin oil-in-water emulsions containing a mixture of surface-active hydrophilic silica nanoparticles and pure nonionic surfactant molecules are reported and compared with those of emulsions stabilized by each emulsifier alone. The importance of the preparation protocol is highlighted. Addition of particles to a surfactant-stabilized emulsion results in the appearance of a small population of large drops due to coalescence, possibly by bridging of adsorbed particles. Addition of surfactant to a particle-stabilized emulsion surprisingly led to increased coalescence too, although the resistance to creaming increased mainly due to an increase in viscosity. Simultaneous emulsification of particles and surfactant led to synergistic stabilization at intermediate concentrations of surfactant; emulsions completely stable to both creaming and coalescence exist at low overall emulsifier concentration. Using the adsorption isotherm of surfactant on particles and the viscosity and optical density of aqueous particle dispersions, we show that the most stable emulsions are formed from dispersions of flocculated, partially hydrophobic particles. From equilibrium contact angle and oil−water interfacial tension measurements, the calculated free energy of adsorption E of a silica particle to the oil−water interface passes through a maximum with respect to surfactant concentration, in line with the emulsion stability optimum. This results from a competition between the influence of particle hydrophobicity and interfacial tension on the magnitude of E.

Tools

History

  • Published In Issue January 30, 2007
  • Received August 25, 2006

Recommend & Share

Related Content

Other ACS content by these authors: