4.6 Article

Preparation of Highly Open Porous Styrene/Acrylonitrile and Styrene/Acrylonitrile/Organoclay Polymerized High Internal Phase Emulsion (PolyHIPE) Foams via Emulsion Templating

Journal

JOURNAL OF APPLIED POLYMER SCIENCE
Volume 119, Issue 6, Pages 3728-3738

Publisher

WILEY
DOI: 10.1002/app.33086

Keywords

copolymerization; emulsion polymerization; nanocomposites

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Highly open porous crosslinked styrene/acrylonitrile (SAN) polymerized high internal phase emulsion (PolyHIPE) foams containing various amounts of acrylonitrile (AN) were prepared by the polymerization of the continuous organic phase of high internal phase emulsions with an 85 vol % aqueous internal phase. The mean diameter of voids varied in the range 12.4-19.8 mu m. The void diameter increased up to 10% AN, but beyond this limit, the diameter decreased. To improve the mechanical properties of the copolymer foams, the organic phase of the emulsion containing 20% AN was reinforced with organomontmorillonites with different surface modifiers. The effects of the organoclay on the equilibrium torque value of the emulsifying systems, as an approximate characteristic of the emulsion viscosity, and on the morphology and mechanical properties of the resulting foam were investigated. Scanning electron micrographs exhibited an open-cell polyHIPE structure for all of the SAN/organoclay polyHIPE foams. The incorporation of organoclays within the emulsion copolymer foam significantly decreased the mean size of voids and intercellular pores compared with those of the copolymer foam without reinforcement. In fact, the presence of organoclay may have acted as a cosurfactant to improve the performance of the nonionic surfactant in the concentrated emulsions. The X-ray diffraction patterns and transmission electron micrographs showed an intercalated nanocomposite structure for the organoclay-reinforced copolymer foams. On the other hand, the addition of a more hydrophilic organoclay, that is, 3 wt % Cloisite30B, to the concentrated emulsion decreased the Young's modulus and significantly improved the crush strength of the emulsion copolymer foam. (C) 2010 Wiley Periodicals, Inc. J Appl Polym Sci 119: 3728-3738, 2011

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