Lowest gelation concentration in a complex-coacervate-driven self-assembly system, achieved by redox-RAFT synthesis of high molecular weight block polyelectrolytes.

Soft Matter

Smart and Sustainable Polymeric Products, Engineering and Technology Institute Groningen, University of Groningen, Nijenborgh 4 9747 AG, The Netherlands.

Published: November 2024

AI Article Synopsis

  • The study aimed to create high molecular weight polyelectrolyte complex (PEC) micelles that can effectively thicken aqueous solutions at low concentrations for industrial use.
  • Redox-initiated RAFT polymerization produced various block polyelectrolytes with significant molecular weights, which formed PEC micelles that exhibited viscoelastic gel characteristics at notably low concentrations.
  • The research compared the effects of different polyelectrolyte architectures on gel behavior, highlighted their responses to environmental factors like salinity and temperature, and utilized techniques like dynamic light scattering to characterize the resulting micelles.

Article Abstract

The objective of this work was to synthesize high molecular weight polyelectrolyte complex (PEC) micelles that are effective in controlling the rheology of aqueous solutions at low concentrations, paving the way for industrial applications of thickeners based on the principle of electrostatic self-assembly. Redox-initiated RAFT (reversible addition-fragmentation chain-transfer) polymerization was used to obtain anionic block polyelectrolytes based on poly(sodium 2-acrylamido-2-methylpropane sulfonate) and poly(acrylamide)-poly(AMPS)--poly(AM) (di-block) and poly(AMPS)--poly(AM)--poly(AMPS) (tri-block), with molecular weights of 237 kDa and 289 kDa and polydispersities of 1.29 and 1.34, respectively. A random poly(AMPS)--poly(AM) copolymer was also synthesized for comparison. PEC micelles were obtained upon mixing with cationic poly(-[3-(dimethylamino)propyl]methacrylamide hydrochloride) - poly(DMAPMA), forming viscoelastic gels at unprecedented low concentrations of <3 wt% for the di-block and <1 wt% for the tri-block, which to date is the lowest demonstrated gelation concentration for a synthetic PEC micelle system. Differences between tri-block and di-block architectures are discussed, with the former being more affected by the addition of salt, which is attributed to percolated network breakdown. The random co-polymer was shown not to be an effective thickener but displayed a surprising lack of phase separation upon coacervation. The assemblies were characterized using dynamic light scattering (DLS) and cryo transmission electron microscopy (cryoTEM), revealing spherical micelles with a diameter of approximately 200 nm for the diblock and a mixture of spherical micelles and network particles for the tri-block PEC micelles. The micelles were not affected by dilution down to a polymer concentration of 7.8 × 10% (approx. 0.03 μM). Responsiveness to salinity, pH, and temperature was studied using DLS, revealing a critical NaCl concentration of 1.1 M for the block copolymer micelles.

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Source
http://dx.doi.org/10.1039/d4sm00763hDOI Listing

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