4.7 Article

Contraction and Coagulation of Spherical Polyelectrolyte Brushes in the Presence of Ag+, Mg2+, and Ca2+ Cations

Journal

MACROMOLECULES
Volume 49, Issue 19, Pages 7460-7468

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.macromol.6b01286

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Funding

  1. Deutsche Forschungsgemeinschaft (DFG) within the Research Training Group Micro- and Nanostructures in Optoelectronics and Photonics [GRK 1464]

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Unlike Na+ cations, which interact with fully neutralized poly(acrylic acid) as purely electrostatic entities, cations like Ag+, Mg2+, and Ca2+ exhibit specific interactions with the COO- residues of anionic polyacrylates. The present work analyzes the interaction of all four cations with a layer of polyacrylate chains grafted onto spherical polystyrene core as an outer shell. First and foremost the analysis answers the question on how these specific interactions influence the nature of the shell and solution behavior of the spherical polyelectrolyte brushes. It could be unambiguously demonstrated that Ag+, Mg2+, and Ca2+ cations induce a drastic shrinking of the polyacrylate shells at cation concentrations lower by 2-3 orders of magnitude compared to the transition of a fully stretched osmotic brush to a shrunken salted brush accomplished with Na+ cations. Ag+ induces a particularly abrupt contraction, which comes close to the annealing of such brushes achieved with a neutralization by protons. Finally, the solution behavior of the brushes in the presence of Ag+ and Ca2+ cations is compared with the respective pattern of molecularly dissolved linear polyacrylate chains in terms of phase diagrams.

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