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Stimuli-responsive polyelectrolyte surfactant complexes for the reversible control of solution viscosity

Del Sorbo, Giuseppe Rosario ; Clemens, Daniel ; Schneck, Emanuel ; Hoffmann, Ingo (2022)
Stimuli-responsive polyelectrolyte surfactant complexes for the reversible control of solution viscosity.
In: Soft Matter, 18 (12)
doi: 10.1039/D1SM01774H
Artikel, Bibliographie

Kurzbeschreibung (Abstract)

Interactions of polyelectrolytes with oppositely charged surfactants can give rise to a large variety of self-assembled structures. Some of these systems cause a drastic increase in solution viscosity, which is related to the surfactant forming aggregates interconnecting several polyelectrolyte chains. For these aggregates to form, the surfactant needs to be sufficiently hydrophobic. Here, we present a system consisting of the anionic surfactant sodium monododecyl phosphate and the cationic cellulose-based polyelectrolyte JR 400. The hydrophobicity of the surfactant can be controlled by the solution's pH. At pH > 12, the surfactant headgroup bears two charges. As a consequence, the solution viscosity decreases drastically by up to two orders of magnitude, while it can be as high as 10 Pa s at lower pH. In this paper, we investigate the changes of the mesoscopic structure of the system which lead to such drastic changes in viscosity using small angle neutron scattering and neutron spin-echo spectroscopy. Such systems are potentially interesting as they allow for a modular design where stimuli responsiveness is introduced by relatively small amounts of surfactant reusing the same simple polyelectrolyte.

Typ des Eintrags: Artikel
Erschienen: 2022
Autor(en): Del Sorbo, Giuseppe Rosario ; Clemens, Daniel ; Schneck, Emanuel ; Hoffmann, Ingo
Art des Eintrags: Bibliographie
Titel: Stimuli-responsive polyelectrolyte surfactant complexes for the reversible control of solution viscosity
Sprache: Englisch
Publikationsjahr: 2 März 2022
Verlag: Royal Society of Chemistry
Titel der Zeitschrift, Zeitung oder Schriftenreihe: Soft Matter
Jahrgang/Volume einer Zeitschrift: 18
(Heft-)Nummer: 12
DOI: 10.1039/D1SM01774H
Kurzbeschreibung (Abstract):

Interactions of polyelectrolytes with oppositely charged surfactants can give rise to a large variety of self-assembled structures. Some of these systems cause a drastic increase in solution viscosity, which is related to the surfactant forming aggregates interconnecting several polyelectrolyte chains. For these aggregates to form, the surfactant needs to be sufficiently hydrophobic. Here, we present a system consisting of the anionic surfactant sodium monododecyl phosphate and the cationic cellulose-based polyelectrolyte JR 400. The hydrophobicity of the surfactant can be controlled by the solution's pH. At pH > 12, the surfactant headgroup bears two charges. As a consequence, the solution viscosity decreases drastically by up to two orders of magnitude, while it can be as high as 10 Pa s at lower pH. In this paper, we investigate the changes of the mesoscopic structure of the system which lead to such drastic changes in viscosity using small angle neutron scattering and neutron spin-echo spectroscopy. Such systems are potentially interesting as they allow for a modular design where stimuli responsiveness is introduced by relatively small amounts of surfactant reusing the same simple polyelectrolyte.

Fachbereich(e)/-gebiet(e): 05 Fachbereich Physik
05 Fachbereich Physik > Institut für Physik Kondensierter Materie (IPKM)
05 Fachbereich Physik > Institut für Physik Kondensierter Materie (IPKM) > Physik biologischer weicher Materie
05 Fachbereich Physik > Institut für Physik Kondensierter Materie (IPKM) > Theorie weicher Materie
Hinterlegungsdatum: 23 Jun 2022 08:52
Letzte Änderung: 06 Dez 2022 11:20
PPN: 502319623
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