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Tuning the particle size and charge density of the crosslinked polystyrene particles

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AbstractWe report the synthesis of charged spherical colloidal particles of poly [styrene‐(co‐2‐propene sulfonic acid)] crosslinked with divinylbenzene by emulsion polymerization. The effects of concentration of both the emulsifier and initiator on the polymerization, particle size, and charge density are studied. The particle size is found to be dependent on both the emulsifier and initiator concentration and their power dependencies are different. Below critical micelle concentration (CMC), the particle size varies significantly within a small range of emulsifier concentration. In contrast, particle size decrease is not very pronounced at the heterogeneous (micellar) particle nucleation regime where the emulsifier concentration is well above of the CMC. The power dependencies of the number of particles on surfactant concentration are explained in the light of conversion–time profile of the polymerization. The surface charge density of the colloidal particles also varies with both the emulsifier and initiator concentration. Both the particle size and charge density show an inverse relation with the molecular weight of the polymer. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008
Title: Tuning the particle size and charge density of the crosslinked polystyrene particles
Description:
AbstractWe report the synthesis of charged spherical colloidal particles of poly [styrene‐(co‐2‐propene sulfonic acid)] crosslinked with divinylbenzene by emulsion polymerization.
The effects of concentration of both the emulsifier and initiator on the polymerization, particle size, and charge density are studied.
The particle size is found to be dependent on both the emulsifier and initiator concentration and their power dependencies are different.
Below critical micelle concentration (CMC), the particle size varies significantly within a small range of emulsifier concentration.
In contrast, particle size decrease is not very pronounced at the heterogeneous (micellar) particle nucleation regime where the emulsifier concentration is well above of the CMC.
The power dependencies of the number of particles on surfactant concentration are explained in the light of conversion–time profile of the polymerization.
The surface charge density of the colloidal particles also varies with both the emulsifier and initiator concentration.
Both the particle size and charge density show an inverse relation with the molecular weight of the polymer.
© 2008 Wiley Periodicals, Inc.
J Appl Polym Sci, 2008.

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