Interfacial rheology of model particles at liquid interfaces and its relation to (bicontinuous) Pickering emulsions.

Interface-dominated materials are commonly encountered in both science and technology, and typical examples include foams and emulsions. Conventionally stabilised by surfactants, emulsions can also be stabilised by micron-sized particles. These so-called Pickering-Ramsden (PR) emulsions have received substantial interest, as they are model arrested systems, rather ubiquitous in industry and promising templates for advanced materials. The mechanical properties of the particle-laden liquid-liquid interface, probed via interfacial rheology, have been shown to play an important role in the formation and stability of PR emulsions. However, the morphological processes which control the formation of emulsions and foams in mixing devices, such as deformation, break-up, and coalescence, are complex and diverse, making it difficult to identify the precise role of the interfacial rheological properties. Interestingly, the role of interfacial rheology in the stability of bicontinuous PR emulsions (bijels) has been virtually unexplored, even though the phase separation process which leads to the formation of these systems is relatively simple and the interfacial deformation processes can be better conceptualised. Hence, the aims of this topical review are twofold. First, we review the existing literature on the interfacial rheology of particle-laden liquid interfaces in rheometrical flows, focussing mainly on model latex suspensions consisting of polystyrene particles carrying sulfate groups, which have been most extensively studied to date. The goal of this part of the review is to identify the generic features of the rheology of such systems. Secondly, we will discuss the relevance of these results to the formation and stability of PR emulsions and bijels.

Separating viscoelastic and compressibility contributions in pressure-area isotherm measurements.

Monolayers of surface active molecules or particles play an important role in biological systems as well as in consumer products. Their properties are controlled by thermodynamics as well as the mechanical properties of the interface itself. For insoluble species forming Langmuir monolayers, surface pressure-area isotherms are typically used to characterize the thermodynamic state. A Langmuir trough equipped with a Wilhelmy plate is often used for such measurements. However, when Langmuir interfaces are compressed and become more structured, the elastic response of these interfaces can interfere with the measurement of the surface pressure-area isotherm, even when the compression speed is slow. Recent reports of compression data for highly elastic interfaces revealed a dependence of the apparent surface pressures on the geometry of the measurement trough. In the present work, this dependence is investigated by considering adequate constitutive models. Since deformations in such compression experiments can be large, linearized versions of the Kelvin-Voigt model do not suffice. We develop a framework for quasi-linear constitutive models by choosing suitable non-linear strain tensors, adequately separating the shear and dilatational effects in a frame invariant manner. The proposed constitutive models can be used as building blocks to describe viscoelastic behavior as well. The geometry dependence in isotherm measurements is then shown to be a consequence of varying contributions of the isotropic surface pressure and extra shear and dilatational elastic stresses. Using these insights, an approach is proposed to obtain the intrinsic surface pressure-area isotherms for elastic interfaces. As a case study, experimental data on graphene oxidesheets at the air-water interface is investigated to evaluate the proposed model.

Characterization of nanoparticles in diluted clear solutions for Silicalite-1 zeolite synthesis using liquid 29Si NMR, SAXS and DLS.

Clear solutions for colloidal Silicalite-1 synthesis were prepared by reacting tetraethylorthosilicate in aqueous tetrapropylammonium hydroxide solution. A dilution series with water resulting in clear solutions with a TEOS ratio TPAOH ratio H2O molar ratio of 25 : 9 : 152 up to 25 : 9 : 15,000 was analysed using liquid 29Si nuclear magnetic resonance (NMR), synchrotron small angle X-ray scattering (SAXS) and dynamic light scattering (DLS). Particle sizes were derived independently from DLS and from the combination of SAXS and NMR. NMR allowed quantitative characterization of silicon distributed over nanoparticles and dissolved oligomeric silicate polyanions. In all samples studied, the majority of silicon (78-90%) was incorporated in the nanoparticle fraction. In concentrated suspensions, silicate oligomers were mostly double-ring species (D3R, D4R, D5R, D6R). Dilution with water caused their depolymerisation. Contrarily, the internal condensation and size of nanoparticles increased with increasing dilution. SAXS revealed a decrease of effective nanoparticle surface charge upon dilution, reducing the effective particle interactions. With DLS, the reduction of nanoparticle interactions could be confirmed monitoring the collective diffusion mode. The observed evolution of nanoparticle characteristics provides insight in the acceleration of the Silicalite-1 crystallization upon dilution, in view of different crystallization models proposed in the literature.

Packing, flipping, and buckling transitions in compressed monolayers of ellipsoidal latex particles.

The behavior of monolayers of monodisperse prolate ellipsoidal latex particles with the same surface chemistry but varying aspect ratio has been studied experimentally. Particle monolayers at an air-water interface were subjected to compression in a Langmuir trough. When surface pressure measurements and microscopy observations were combined, possible structural transitions were evaluated. Ellipsoids of a sufficiently large aspect ratio display a less abrupt increase in the compression isotherms than spherical particles. Microscopic observations reveal that a sequence of transitions is responsible for this more gradual increase of the surface pressure. When a percolating aggregate network is used as the starting point, locally ordered regions appear progressively. When it reaches a certain surface pressure, the system "jams", and in-plane rearrangements are no longer possible at this point. A highly localized yielding of the particle network is observed. The compressional stress is relieved by flipping the ellipsoids into an upright position and by expelling particles from the monolayer. The latter does not occur for spherical particles with similar dimensions and surface chemistry. In the final stage of compression, buckling of the monolayer as a whole was observed. The effect of aspect ratio on the pressure area isotherms and on the obtained percolation and packing thresholds was quantified.

Multi length scale analysis of the microstructure in sticky sphere dispersions during shear flow.

The effect of shear flow on the microstructure in a weakly aggregated suspension is investigated. Monodisperse small silica particles with a grafted layer of 1-octadecanol are dispersed in n-tetradecane, yielding a thermoreversible sticky sphere model suspension. A combination of small angle light scattering and ultra small and small-angle X-ray scattering techniques have been used, in situ and time resolved, to study the flow-induced anisotropy of the microstructure. In this manner, the length scales from the single particle size to that of the spatial organization of the aggregates can be covered. Harmonic expansion of the structure factor demonstrates that anisotropy develops in the microstructure on all relevant length scales. Possible real space interpretations of the scattering information are discussed in conjunction with implications for the nonlinear rheological behavior.

Prediction and observation of sustained oscillations in a sheared liquid crystalline polymer.

Experimental observations of sustained oscillations of both shear stress and first normal stress differences are reported in flowing liquid crystalline polymers in a limited range of shear rates. The results can be described by considering the response of a rigid-rod model. Depending on the initial conditions, the frequency spectrum of the stress signal contains either one or two characteristic frequencies. This can be explained by the occurrence of either pure "wagging" or the coexistence of wagging and "log-rolling" behavior of the director.

Structure and rheology during shear-induced crystallization of a latex suspension.

Microstructure and rheology of a concentrated sterically stabilized colloidal suspension undergoing flow-induced ordering was studied by combined small-angle x-ray scattering and rheometry. This system is known to form bundlelike structures at high stress values in continuous shear flow. Under large amplitude oscillatory flow, hexagonal close-packed crystalline domains are formed within 1 sec of the inception of shear. In the intermediate range of frequencies and amplitudes, a nearly perfect hexagonally close-packed layer structure was observed after the cessation of flow. Lower frequencies or stress amplitudes resulted in polycrystals and, on the other hand, high frequencies or stress amplitudes led to partial melting of the layered structure. During the oscillatory flow, the intensity of the Bragg peaks showed pronounced oscillations.

Flow-Induced Anisotropy in Mixtures of Associative Polymers and Latex Particles.

The effect of associative polymers on the structure and rheological behavior of colloidal suspensions is discussed. Adding associative polymer is known to increase the viscosity of the suspensions. At high shear rates the increase is close to what could be expected on the basis of the hydrodynamic effects of the added polymer. At low shear rates the viscosity increases much more. Small-angle light scattering (SALS) during flow is used here to investigate the underlying structural mechanisms. The SALS patterns indicate that the associative polymer changes the particulate structure: characteristic butterfly patterns appear even at relatively low particle volume fractions. They are not present in the suspensions without associative polymer. The patterns indicate that fluctuations in particle concentration are more pronounced in the flow direction than in the vorticity direction and that anisotropic particulate structures with an orientation along the vorticity direction develop. The evolution of their characteristic length scale during flow has been followed over time. Changing the hydrophilic part of the polymer from polyacrylamide to polyacrylic acid induces stronger associative interactions. In the suspensions this results in a reduction of the relative viscosity rather than an increase. The difference in degree of associativity between the polymers also has an effect on the SALS patterns in the suspensions both at rest and during flow. The rheology as well as the SALS suggest the presence of a strong polymer network in the second system. The competition between adsorption of the associative polymer on the particles with the intermolecular associations between the polymer chains seems to be responsible for the observed differences. Copyright 2000 Academic Press.

Large-Scale Bundle Ordering in Sterically Stabilized Latices.

Time-resolved small-angle light scattering and linear conservative dichroism measurements are presented for concentrated, sterically stabilized, aqueous latices under simple shear flow. At low stress levels, flow causes a mild distortion of the liquid-like structure in colloidally stable dispersions, which is quite well understood. In this paper flow-induced structures are investigated in concentrated dispersions when the system is brought far from equilibrium by means of hydrodynamic forces. At high stress levels various structural changes have been predicted by numerical simulation, among others string phases oriented in the flow direction. Here, experimental results are reported on a bundle-like ordering in very dense systems, which involves a length scale much larger than that of a single string of particles. Two latices, with different particle sizes and different thicknesses of the stabilizing layer, are compared. The occurrence of the bundle-like ordering is related to the rheological behavior: it causes a significant decrease in viscosity. It is shown that the presence of this phase results in a structural hysteresis, which explains a thixotropic behavior that is encountered in some stable colloidal suspensions. Also the relaxation behavior of the bundle-like phases has been studied. Interparticle forces are found to have a very strong effect on the relaxation time scales. Copyright 1999 Academic Press.