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Oscillatory Structural Forces Across Dispersions of Micelles With Variable Surface Charge

Ludwig, Michael ; Ritzert, Philipp ; Geisler, Ramsia ; Prévost, Sylvain ; Klitzing, Regine von (2022)
Oscillatory Structural Forces Across Dispersions of Micelles With Variable Surface Charge.
In: Frontiers in Soft Matter, 2022, 2
doi: 10.26083/tuprints-00022087
Artikel, Zweitveröffentlichung, Verlagsversion

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Kurzbeschreibung (Abstract)

When two surfaces interact across colloidal dispersions, oscillatory structural forces often arise due to an ordering of colloidal particles. Although this type of forces was intensively studied, the effect of the surface charge of the colloidal particles is still poorly understood. In the present study, the surface charge of colloidal particles is varied by changing the ratio of nonionic (Tween20) and anionic (sodium dodecyl sulfate, SDS) surfactants of micellar dispersions. The same micellar systems were previously characterised with small-angle neutron scattering (SANS) by the authors, revealing that mixed nonionic-anionic surfactant micelles with variable surface charge form. The present paper addresses the ordering phenomena of the micellar systems under confinement. Therefore, forces across these dispersions were measured for varying surface charges and volume fractions of the micelles, using colloidal-probe atomic force microscopy (CP-AFM). The combination of SANS and CP-AFM experiments allows the dispersions structure in bulk and under geometrical confinement to be compared in terms of the characteristic interparticle distance, correlation length, and ordering strength: In bulk and under confinement, the characteristic intermicellar distance increases by introducing surface charges to micelles until the electrostatic repulsion forces the micelles into a specific ordering. There, the characteristic intermicellar distance purely relates to the micelle volume fraction ϕ as ∝ ϕ−1/3. While in dispersions of uncharged micelles the characteristic intermicellar distance is reduced from bulk to confinement, no such compressibility is observed once the micelles are charged. Furthermore, variation of the micelles surface charge has only little effect on the correlation length of the micelles ordering which is mainly governed by hard-sphere interactions, especially in concentrated dispersions. Introducing surface charges, however, enhances the ordering strength (i.e., the amplitude) of oscillatory structural forces due to stronger electrostatic repulsions of the micelles with the equally charged confining surface. This surface-induced effect is not represented in bulk scattering experiments.

Typ des Eintrags: Artikel
Erschienen: 2022
Autor(en): Ludwig, Michael ; Ritzert, Philipp ; Geisler, Ramsia ; Prévost, Sylvain ; Klitzing, Regine von
Art des Eintrags: Zweitveröffentlichung
Titel: Oscillatory Structural Forces Across Dispersions of Micelles With Variable Surface Charge
Sprache: Englisch
Publikationsjahr: 2022
Ort: Darmstadt
Publikationsdatum der Erstveröffentlichung: 2022
Verlag: Frontiers
Titel der Zeitschrift, Zeitung oder Schriftenreihe: Frontiers in Soft Matter
Jahrgang/Volume einer Zeitschrift: 2
Kollation: 11 Seiten
DOI: 10.26083/tuprints-00022087
URL / URN: https://tuprints.ulb.tu-darmstadt.de/22087
Zugehörige Links:
Herkunft: Zweitveröffentlichung aus gefördertem Golden Open Access
Kurzbeschreibung (Abstract):

When two surfaces interact across colloidal dispersions, oscillatory structural forces often arise due to an ordering of colloidal particles. Although this type of forces was intensively studied, the effect of the surface charge of the colloidal particles is still poorly understood. In the present study, the surface charge of colloidal particles is varied by changing the ratio of nonionic (Tween20) and anionic (sodium dodecyl sulfate, SDS) surfactants of micellar dispersions. The same micellar systems were previously characterised with small-angle neutron scattering (SANS) by the authors, revealing that mixed nonionic-anionic surfactant micelles with variable surface charge form. The present paper addresses the ordering phenomena of the micellar systems under confinement. Therefore, forces across these dispersions were measured for varying surface charges and volume fractions of the micelles, using colloidal-probe atomic force microscopy (CP-AFM). The combination of SANS and CP-AFM experiments allows the dispersions structure in bulk and under geometrical confinement to be compared in terms of the characteristic interparticle distance, correlation length, and ordering strength: In bulk and under confinement, the characteristic intermicellar distance increases by introducing surface charges to micelles until the electrostatic repulsion forces the micelles into a specific ordering. There, the characteristic intermicellar distance purely relates to the micelle volume fraction ϕ as ∝ ϕ−1/3. While in dispersions of uncharged micelles the characteristic intermicellar distance is reduced from bulk to confinement, no such compressibility is observed once the micelles are charged. Furthermore, variation of the micelles surface charge has only little effect on the correlation length of the micelles ordering which is mainly governed by hard-sphere interactions, especially in concentrated dispersions. Introducing surface charges, however, enhances the ordering strength (i.e., the amplitude) of oscillatory structural forces due to stronger electrostatic repulsions of the micelles with the equally charged confining surface. This surface-induced effect is not represented in bulk scattering experiments.

Freie Schlagworte: micellar dispersions, small-angle neutron scattering, structural force, depletion force, direct force measurements, atomic force microscopy
Status: Verlagsversion
URN: urn:nbn:de:tuda-tuprints-220879
Sachgruppe der Dewey Dezimalklassifikatin (DDC): 500 Naturwissenschaften und Mathematik > 530 Physik
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) > Soft Matter at Interfaces (SMI)
Hinterlegungsdatum: 26 Aug 2022 12:04
Letzte Änderung: 29 Aug 2022 08:15
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