4.6 Article

Complexes of Charged-Neutral Block Copolymers and Surfactants: Process-Dependent Features and Long-Term Stability of Their Aqueous Dispersions

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LANGMUIR
卷 39, 期 11, 页码 4113-4124

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AMER CHEMICAL SOC
DOI: 10.1021/acs.langmuir.2c03500

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Aqueous dispersions of charged-neutral block copolymers complexed with an oppositely charged surfactant were prepared using different approaches. The dispersions prepared by the simple mixing of two solutions displayed nanometric spherical particles with disordered cores and poor colloidal stability. On the other hand, dispersions prepared from freeze-dried complex salt had anisometric particles that were large enough to sustain micellar cubic cores and showed long-time colloidal stability. The results highlight the importance of the preparation procedure in controlling the physicochemical properties of dispersed particles.
Aqueous dispersions of charged-neutral block copolymers (poly(acrylamide)-b-poly(acrylate)) complexed with an oppositely charged surfactant (dodecyltrimethylammonium) have been prepared by different approaches: the simple mixing of two solutions (MS approach) containing the block copolymer and surfactant, with their respective simple counterions, and dispersion of a freeze-dried complex salt prepared in the absence of simple counterions (CS approach). The CS particles were investigated under different conditions: dispersion of a CS in salt-free water and dispersion of a CS in a dilute salt solution, the latter condition yielding dispersions with the same composition as the MS process. Additionally, aged dispersions (up to 6 months) and dispersed complexes of the polyacrylate homopolymer and dodecyltrimethylammonium surfactant were evaluated. By employing different characterization techniques, it was seen that dispersions prepared by the MS approach display nanometric spherical particles with disordered cores, and poor colloidal stability, partially caused by the absence of surface charge (zeta -potential close to zero). Oppositely, anisometric particles were formed in CS dispersions and were large enough to sustain micellar cubic cores. The CS particles presented long-time colloidal stability, partially due to a net negative surface charge, but the stability varied with the length of the neutral block composing the corona. Our results demonstrate that all dispersed particles are metastable structures, with physicochemical properties strongly dependent on the preparation procedure, thus making these particles suitable for fundamental studies and potential applications where accurate control of their properties, including size, shape, internal structure, and stability, is desired.

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