The foam film stability of polyelectrolyte/surfactant mixtures is rationalized using structural data from neutron reflectometry for the first time.

This paper addresses the effect of polyelectrolyte stiffness on the surface structure of polyelectrolyte (P)/surfactant (S) mixtures. Therefore, two different anionic Ps with different intrinsic persistence length l P are studied while varying the salt concentration (0–10–2 M). Either monosulfonated polyphenylene sulfone (sPSO2-220, l P ∼20 nm) or sodium poly­(styrenesulfonate) (PSS, l P ∼1 nm) is mixed with the cationic surfactant tetradecyltrimethylammonium bromide (C14TAB) well below its critical micelle concentration and studied with tensiometry and neutron reflectivity experiments. We kept the S concentration (10–4 M) constant, while we varied the P concentration (10–5–10–3 M of the monomer, denoted as monoM). P and S adsorb at the air/water interface for all studied mixtures. Around the bulk stoichiometric mixing point (BSMP), PSS/C14TAB mixtures lose their surface activity, whereas sPSO2-220/C14TAB mixtures form extended structures perpendicular to the surface (meaning a layer of S with attached P and additional layers of P and S underneath instead of only a monolayer of S with P). Considering the different P monomer structures as well as the impact of salt, we identified the driving force for the formation of these extended structures: compensation of all interfacial charges (P/S ratio ∼1) to maximize the gain of entropy. By increasing the flexibility of P, we can tune the interfacial structures from extended structures to monolayers. These findings may help improve applications based on the adsorption of P/S mixtures in the fields of cosmetic or oil recovery.

aThe complex interaction of polyelectrolyte multilayers (PEMs) physisorbed onto end-grafted polymer brushes with focus on the temperature-responsive behavior of the system is addressed in this work. The investigated brush/multilayer composite consists of a poly(styrene sulfonate)/poly(diallyldimethylammonium chloride) (PSS/PDADMAC) multilayer deposited onto the poly(N-isopropylacrylamide-bdimethylaminoethyl methacrylate) P(NIPAM-b-DMAEMA) brush. Ellipsometry and neutron reflectometry were used to monitor the brush collapse with the thickness decrease as a function of temperature and the change in the monomer distribution perpendicular to the substrate at temperatures below, across and above the phase transition, respectively. It was found that the adsorption of PEMs onto polymer brushes had a hydrophobization effect on PDMAEMA, inducing the shift of its phase transition to lower temperatures, but without suppressing its temperature-responsiveness. Moreover, the diffusion of the free polyelectrolyte chains inside the charged brush was proved by comparing the neutron scattering length density profile of pure and the corresponding PEM-capped brushes, eased by the enhanced contrast between hydrogenated brushes and deuterated PSS chains. The results presented herein demonstrate the possibility of combining a temperature-responsive brush with polyelectrolyte multilayers without quenching the responsive behavior, even though significant interpolyelectrolyte interactions are present. This is of importance for the design of multicompartment coatings, where the brush can be used as a reservoir for the controlled release of substances and the multilayer on the top as a membrane to control the diffusion in/out by applying different stimuli.

The paper addresses the swelling of polyelectrolyte multilayers (PEMs) at varying humidity. In particular, a new model will be presented, which takes the gradual filling of voids into account. Absorption of water results in PEM swelling. This absorbed water can be distinguished into swelling and void water. Swelling water leads to an increase in thickness and a change of the optical properties of PEMs, while the void water results only in a change of the optical properties. In former studies, neutron reflectometry was used to distinguish between swelling and void water. However, as we show in this study, it is possible to resolve the two different kinds of water in PEMs by ellipsometry, a much simpler tool. The present study evaluates and interprets the refractive index of polystyrenesulfonate/polydiallyldimethylammonium chloride (PSS/PDADMAC) PEMs. Both the swelling behavior and the refractive index change as a function of relative humidity and were found to be independent of the layer number. The void model and the extended void model were used to describe the data. The void model allows fitting the experimentally determined refractive index at humidity beyond 20% RH but fails for humidity lower than 20% RH. Therefore, we modified the existing model in order to account for air-water exchange. The extended void model assumes a gradual air-water exchange at low h and describes the refractive index over the entire humidity range in a precise way. Up to 30% RH, air and water coexist. Above this threshold, the voids are completely filled with water and this threshold does not change either with layer number or with the outermost layer. Furthermore, this model allows the determination of the volume fraction of the voids (0.05 ± 0.01) and the refractive index of the pure polymer matter (1.592 ± 0.002).

Responsive aqueous foams are very interesting from a fundamental point of view and for various applications like foam flooding or foam flotation. In this study thermoresponsive microgels (MGs) made from...