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    A highly hydrophobic anionic surfactant at oil–water, water–polymer and oil–polymer interfaces: Implications for spreading coefficients, polymer interactions and microencapsulation via internal phase separation

    Year: 2013

    Journal: Colloids and Surfaces A: Physicochemical and Engineering Aspects, Volume 436, 5 September 2013, Pages 1048–1059, 20131119

    Authors: Markus Andersson Trojera 1,Azmi Mohamed 2 3, Julian Eastoe 2

    Organizations: 1 Department of Chemical and Biological Engineering, Applied Surface Chemistry, Chalmers University of Technology, Göteborg, Sweden, 2 School of Chemistry, University of Bristol, Cantock's Close, Bristol BS8 1TS, UK, 3 Department of Chemistry, Faculty of Science and Mathematics, Universiti Pendidikan Sultan Idris, 35900 Tanjong Malim, Perak, Malaysia

    Multicore–shell particles consisting of a poly(methyl methacrylate) shell and multiple dodecane cores have been prepared via the internal phase separation method using the oil-soluble anionic surfactant sodium 1,5-dioxo-1,5-bis(3,5,5-trimethylhexylocy)-3-((3,5,5 trimethylhexyloxy)carbonyl)pentane-2-sulfonate (TC4) and the water-soluble polycation poly(diallyldimethylammonium chloride) (PDADMAC) in combination as a dispersant pair. The multicore–shell particles have been investigated using SEM, light microscopy and microelectrophoresis. The detailed influence of TC4 on the oil–water, water–polymer and oil–polymer interfaces and its interaction with PDADMAC have been investigated using a quartz crystal microbalance with dissipation monitoring (QCM-D) and different optical tensiometry methods. TC4 stabilizes in particular the polymer–water interface in the presence of PDADMAC instead of the oil–water interface in contrast to water-soluble surfactants. In addition, the oil–polymer interface is stabilized by TC4 which prevents coalescence of the oil droplets and leads to multicore–shell morphology rather than single core–shell.