Amphiphilic Block-Random Copolymers: Self-Folding Behavior and Stabilizers in Emulsion Polymerization
Polystyrene-b-[polystyrene-r-poly(acrylic acid)] block-random copolymers have been synthesized at various molecular weights (7000–23 200 g/mol) and with compositions between 6 and 39 mol % acrylic acid by nitroxide-mediated polymerization. Emulsion polymerizations of styrene stabilized by block-ran...
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Veröffentlicht in: | Macromolecules 2019-06, Vol.52 (12), p.4510-4519 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Polystyrene-b-[polystyrene-r-poly(acrylic acid)] block-random copolymers have been synthesized at various molecular weights (7000–23 200 g/mol) and with compositions between 6 and 39 mol % acrylic acid by nitroxide-mediated polymerization. Emulsion polymerizations of styrene stabilized by block-random copolymers yielded stable latexes at stabilizer concentrations ≥3 wt % based on monomer. A series of emulsion polymerizations with varying stabilizer content suggests that a novel nucleation mechanism occurs in block-random copolymer-stabilized emulsion polymerizations, exhibiting distinctly different behaviors from block copolymers or conventional small-molecule surfactants. Moreover, alkaline aqueous dispersions of the block-random copolymers were prepared with ease up to concentrations of 300 g/L, whereas similar block copolymers are limited to ∼1 g/L. Analysis of the dispersions via dynamic light scattering and atomic force microscopy suggests that single-chain nanoparticles form via a self-folding process with hydrodynamic diameters between 2.4 and 5 nm. The novel stabilizer structures may be tuned for rapid dispersion through their anchoring block [polystyrene] and high stabilization efficiency through the stabilizing block [polystyrene-r-poly(acrylic acid)]. |
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ISSN: | 0024-9297 1520-5835 |
DOI: | 10.1021/acs.macromol.9b00519 |