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In relation to this article, we declare that there is no conflict of interest.
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Received October 10, 2002
Accepted December 9, 2002
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Monodisperse Micron-sized Polystyrene Particles by Seeded Polymerization Using Reactive Macrosurfactants

Cosmetics Research Institute, Pacific Corporation R&D Center, 314-1, Bora-ri, Kiheung-eup,Yongin-si, Kyunggi-do 449-900, Korea 1Division of Chemical Engineering, College of Engineering, Hanyang University, Seoul 133-791, Korea 2Department of Chemical Engineering, Samchok National University, Samchok, Kangwon-do 245-711, Korea
Korean Journal of Chemical Engineering, March 2003, 20(2), 399-406(8), 10.1007/BF02697258
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Abstract

Monodisperse micron-sized polystyrene particles could be prepared through a two-staged seeded swelling and polymerization method using reactive surfactants. The seed was obtained by emulsifier-free emulsion polymerization. To prepare conventional surfactant-free monomer emulsion droplet in swelling process, a tri-block diol diacrylate (t-BDDA), which is poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) tri-block copolymer containing two chain ends capped with acryloyl chloride, was employed as a reactive surfactant instead of conventional surfactants. Thermodynamic consideration of the effect of monomer droplet size and interfacial tension on the swelling process ensured that two-staged monomer swelling could be effectively performed by using t-BDDA as a surface-active macromonomer. From the surface tension measurement and optical microscope observation, it was found that the t-BDDA had a favorable surface activity when the monomer emulsion was prepared under its cloud point. From the X-ray photoelectron spectroscopy, it was found that most of the t-BDDA resided on the final particle surfaces.

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