Abstract:Foam films display exciting systems as on one hand they dictate the performance of macroscopic foams and on the other hand they allow studies of surface forces. With regard to surface forces, we attempt to disentangle the effect of the foam film surfaces and the foam film bulk. For that, we study the influence of salt (LiBr) on foam films formed by mixtures of oppositely charged polyelectrolyte and surfactant: anionic monosulfonated polyphenylene sulfone (sPSO 2 -220) and cationic tetradecyltrimethylammonium b… Show more
“…Foams of P/S aggregates are mainly stabilized through electrostatic disjoining forces 41 or steric repulsion 8,9 as well as due to Pickering effects with larger particles. 13 When the surfactants are in the E state the disjoining pressure between gas bubbles is sufficiently high but is reduced drastically for the Z isomer where surfactant desorption from the interface (Fig.…”
Section: N Aap/pdadmac Mixtures For Stabilization Of Aqueous Foammentioning
confidence: 99%
“…[4][5][6][7] Owing to their widespread use in applications, the properties of P/S mixtures with classical surfactants like dodecylsulfate or alkylammonium in bulk solutions and at interfaces are studied extensively to the present day. [5][6][7][8][9][10][11][12] Using different P/S mixing ratios allows one to tailor soft matter properties such as the size of the P/S aggregates that form after mixing or the stability of aqueous foams.…”
In many applications of polyelectrolyte/surfactant (P/S) mixtures, it is difficult to fine-tune them after mixing the components without changing the sample composition, e.g. pH or the ionic strength. Here we...
“…Foams of P/S aggregates are mainly stabilized through electrostatic disjoining forces 41 or steric repulsion 8,9 as well as due to Pickering effects with larger particles. 13 When the surfactants are in the E state the disjoining pressure between gas bubbles is sufficiently high but is reduced drastically for the Z isomer where surfactant desorption from the interface (Fig.…”
Section: N Aap/pdadmac Mixtures For Stabilization Of Aqueous Foammentioning
confidence: 99%
“…[4][5][6][7] Owing to their widespread use in applications, the properties of P/S mixtures with classical surfactants like dodecylsulfate or alkylammonium in bulk solutions and at interfaces are studied extensively to the present day. [5][6][7][8][9][10][11][12] Using different P/S mixing ratios allows one to tailor soft matter properties such as the size of the P/S aggregates that form after mixing or the stability of aqueous foams.…”
In many applications of polyelectrolyte/surfactant (P/S) mixtures, it is difficult to fine-tune them after mixing the components without changing the sample composition, e.g. pH or the ionic strength. Here we...
“…[4][5][6][7] Owing to their widespread use in applications, the properties of P/S mixtures with classical surfactants like dodecylsulfate or alkylammonium in bulk solutions and at interfaces are studied extensively to the present day. [5][6][7][8][9][10][11][12] Using different P/S mixing ratios allows one to tailor soft matter properties such as the size of the P/S aggregates that form after mixing or the stability of aqueous foam. However, these properties are notoriously difficult to change after P/S mixtures have been prepared, where only drastic changes in chemical composition e.g., pH values, or in the ionic strengths are useful triggers.…”
In many applications of polyelectrolyte/surfactant (P/S) mixtures, it is difficult to fine-tune them after mixing the components without changing the sample composition, e.g. pH or the ionic strength. Here we report on a new approach where we use photoswitchable surfactants to enable drastic changes in both the bulk and interfacial properties. Poly(diallyldimethylammonium chloride) (PDADMAC) mixtures with three alkyl-arylazopyrazole butyl sulfonates (CnAAP) with -H, -butyl and -octyl tails are applied and E/Z photoisomerization of the surfactants is used to cause substantially different hydrophobic interactions between the surfactants and PDADMAC. This affects significantly the P/S binding and allows for tuning both the bulk and interfacial properties of PDADMAC/CnAAP mixtures through light irradiation. For that, we have fixed the surfactant concentrations at values where they exhibit pronounced surface tension changes upon E/Z photoisomerization with 365 nm UV light (Z) and 520 nm green (E) light and have varied the PDADMAC concentration. The electrophoretic mobility can be largely tuned by photoisomerisation of CnAAP surfactants and P/S aggregates, which can even exhibit a charge reversal from negative to positive values or vice versa. In addition, low colloidal stability at equimolar concentrations of PDADMAC with CnAAP surfactants in the E configuration lead to the formation of large aggregates in the bulk which can be redissolved by irradiation with UV light when the surfactant‘s alkyl chain is short enough (C0AAP). Vibrational sum-frequency generation (SFG) reveals changes at the interface similar to the bulk, where the charging state at air-water interfaces can be modified with light irradiation. Using SFG spectroscopy, we interrogated the O-H stretching modes of interfacial H2O and provide qualitative information on surface charging that is complemented by neutron reflectometry, from which we resolved the surface excess of PDADMAC and CnAAP at the air-water interface, independently.
“…On the other hand, polyelectrolyte/surfactant complexes are well-known for forming interfacial networks at gas/liquid and liquid/liquid interfaces through physical cross-linking. , These complexes are formed by the electrostatic interaction between oppositely charged polyelectrolytes and surfactants, resulting in the formation of a stable network at the interface. The main function of surfactants in this context is to increase the local concentration of hydrophobic cargo by forming self-assemblies that can encapsulate the cargo. , This is achieved through hydrophobic interactions between the surfactant molecules and the hydrophobic cargo.…”
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