We have characterized the dissolution state of microcrystalline cellulose (MCC) in aqueous 40 wt% tetrabutylammonium hydroxide (TBAH) using a combination of light and small angle X-ray scattering, up to 0.1 g cm−3.

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We have investigated the spontaneous self-assembly of solid, mesostructured films that form at the air-solution interface on solutions containing a neutral water-soluble polymer and catanionic surfactant mixtures of hexadecyl-trimethylammonium bromide (CTAB) and sodium dodecylsulphate (SDS). The formation processes and structures were probed using neutron reflectivity, X-ray reflectivity, off-specular time-resolved scattering, and grazing incidence diffraction. The mesostructures of films prepared with polyethylene oxide, polyethylenimine, and polyacrylamide at various cationic/anionic surfactant molar ratios are compared. The results suggest that polymers having a weak interaction with the surfactants cause a depletion aggregation process that results in a lamellar phase, whereas polymers having a stronger interaction with the surfactants produce more complex mesostructures in the films.

The structure and dynamics of nanostructure films formed by mixtures of soy phosphatidylcholine and glycerol dioleate at the silicon-aqueous interface were studied by grazing incidence neutron spin echo spectroscopy (GINSES), specular and off-specular neutron reflectometry, and small-angle X-ray diffraction. Reverse hexagonal (H) and micellar cubic phase (Fd3m) layers at the solid-liquid interface have been identified with neutron reflectometry measurements. A preferred orientation of the liquid crystalline (LC) domains was observed only for the anisotropic H phase. The size of the LC domains was found to be about 1 micrometer as estimated from the width of the diffraction peaks. GINSES revealed that the cubic phase forms rather rigid films. In comparison, the H film was more flexible, appearing as a modified undulation spectrum of the cylinders due to the interaction with the substrate.

Polymer/silica composite films, stable to calcination, were produced using catanionic surfactant mixtures (hexadecyltrimethylammonium bromide (CTAB) and sodium dodecyl sulfate (SDS)) and polymers (polyethylenimine (PEI) or polyacrylamide (PAAm)) at the air/water interface. Film formation processes were probed by time-resolved neutron reflectivity measurements. Grazing incidence X-ray diffraction (GID) measurements indicate that the mesophase geometry of the interfacial films could be controlled to give lamellar, 2D hexagonal, and several cubic phases (Pn3¯m, Fm3¯m, and Im3¯m) by varying the polyelectrolyte molecular weight, polyelectrolyte chemical nature, or the cationic:anionic surfactant molar ratio. On the basis of GID results, a phase diagram for the catanionic surfactant/polyelectrolyte/TMOS film system was drawn. These films can be easily removed from the interface and mesoporous silica films which retain the film geometry can be obtained after calcination; moreover, this film preparation method provides a simple way to impart polymer functionality into the mesostructured silica wall, which means these films have potential applications in a variety of fields such as catalysis, molecular separation, and drug delivery.