TY - JOUR
T1 - Synthesis of polystyrene-silica composite particles via one-step nanoparticle-stabilized emulsion polymerization
AU - Ma, Huan
AU - Dai, Lenore L.
N1 - Funding Information:
We acknowledge the Department of Chemical Engineering, the Department of Chemistry, and the Imaging Center at Texas Tech University for instrumental usage and the National Science Foundation for financial support (CBET-0625191 and CBET-0644850).
PY - 2009/5/15
Y1 - 2009/5/15
N2 - Polystyrene-silica core-shell composite particles are prepared by one-step emulsion polymerization with a nonionic initiator VA-086, solely stabilized by silica nanoparticles. The silica nanoparticles are successfully incorporated as the shell, likely due to the fact that the nanoparticles are thermodynamically favorable to adsorb and remain at the liquid-liquid interfaces during the emulsion polymerization. The silica content, determined by thermogravimetric analysis, is approximately 20 wt% in the composite particles. In addition, we further explore the polymerization mechanism by studying the particle growth as a function of initiator concentration and reaction time: when the initiator/monomer ratio is increased from 0.83 to 2.5 wt%, the particle size at 24 h reaction time decreases for a fixed monomer amount, possibly due to a larger number of nuclei at the initial stage of polymerization. Further increasing the initiator/monomer ratio to 4.2 wt% does not continually decrease the particle size, which may be limited by the stabilization provided by a fixed concentration of silica nanoparticles. The surface coverage also changes with initiator concentration and reaction time although the underlying mechanism is not fully understood.
AB - Polystyrene-silica core-shell composite particles are prepared by one-step emulsion polymerization with a nonionic initiator VA-086, solely stabilized by silica nanoparticles. The silica nanoparticles are successfully incorporated as the shell, likely due to the fact that the nanoparticles are thermodynamically favorable to adsorb and remain at the liquid-liquid interfaces during the emulsion polymerization. The silica content, determined by thermogravimetric analysis, is approximately 20 wt% in the composite particles. In addition, we further explore the polymerization mechanism by studying the particle growth as a function of initiator concentration and reaction time: when the initiator/monomer ratio is increased from 0.83 to 2.5 wt%, the particle size at 24 h reaction time decreases for a fixed monomer amount, possibly due to a larger number of nuclei at the initial stage of polymerization. Further increasing the initiator/monomer ratio to 4.2 wt% does not continually decrease the particle size, which may be limited by the stabilization provided by a fixed concentration of silica nanoparticles. The surface coverage also changes with initiator concentration and reaction time although the underlying mechanism is not fully understood.
KW - Core-shell composite particles
KW - Emulsion polymerization
KW - Nanoparticle stabilizer
KW - Non-ionic initiator
KW - VA-086
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U2 - 10.1016/j.jcis.2009.02.007
DO - 10.1016/j.jcis.2009.02.007
M3 - Article
C2 - 19249057
AN - SCOPUS:63249132174
SN - 0021-9797
VL - 333
SP - 807
EP - 811
JO - Journal of Colloid And Interface Science
JF - Journal of Colloid And Interface Science
IS - 2
ER -