Effect of the acrylic acid content on the permeability and water uptake of latex films

Acrylic acid (AA) is a monomer commonly employed in emulsion polymerization to provide electrostatic colloidal stability and improve specific film performance. The addition of AA not only modifies the kinetics of the polymerization, but also it takes part in the interaction between colloidal particles, which has a strong influence on their packing and consequent latex film properties. In this contribution a theoretical modeling of the latex film formation is presented and compared to experimental results: water vapor permeability and latex film capacitance are studied as a function of AA content. It has been shown that water uptake is mainly affected by film morphology which in turn is defined by intercolloidal interaction and drying rate.Comment: 16 pages, 7 figure

Measuring every particle's size from three-dimensional imaging experiments

Often experimentalists study colloidal suspensions that are nominally monodisperse. In reality these samples have a polydispersity of 4-10%. At the level of an individual particle, the consequences of this polydispersity are unknown as it is difficult to measure an individual particle size from microscopy. We propose a general method to estimate individual particle radii within a moderately concentrated colloidal suspension observed with confocal microscopy. We confirm the validity of our method by numerical simulations of four major systems: random close packing, colloidal gels, nominally monodisperse dense samples, and nominally binary dense samples. We then apply our method to experimental data, and demonstrate the utility of this method with results from four case studies. In the first, we demonstrate that we can recover the full particle size distribution {\it in situ}. In the second, we show that accounting for particle size leads to more accurate structural information in a random close packed sample. In the third, we show that crystal nucleation occurs in locally monodisperse regions. In the fourth, we show that particle mobility in a dense sample is correlated to the local volume fraction.Comment: 7 pages, 5 figure

Quantitative imaging of concentrated suspensions under flow

We review recent advances in imaging the flow of concentrated suspensions, focussing on the use of confocal microscopy to obtain time-resolved information on the single-particle level in these systems. After motivating the need for quantitative (confocal) imaging in suspension rheology, we briefly describe the particles, sample environments, microscopy tools and analysis algorithms needed to perform this kind of experiments. The second part of the review focusses on microscopic aspects of the flow of concentrated model hard-sphere-like suspensions, and the relation to non-linear rheological phenomena such as yielding, shear localization, wall slip and shear-induced ordering. Both Brownian and non-Brownian systems will be described. We show how quantitative imaging can improve our understanding of the connection between microscopic dynamics and bulk flow.Comment: Review on imaging hard-sphere suspensions, incl summary of methodology. Submitted for special volume 'High Solid Dispersions' ed. M. Cloitre, Vol. xx of 'Advances and Polymer Science' (Springer, Berlin, 2009); 22 pages, 16 fig

Dipolar colloids in apolar media: direct microscopy of two-dimensional suspensions

Spherical colloids, in an absence of external fields, are commonly assumed to interact solely through rotationally-invariant potentials, u(r). While the presence of permanent dipoles in aqueous suspensions has been previously suggested by some experiments, the rotational degrees of freedom of spherical colloids are typically neglected. We prove, by direct experiments, the presence of permanent dipoles in commonly used spherical poly(methyl methacrylate) (PMMA) colloids, suspended in an apolar organic medium. We study, by a combination of direct confocal microscopy, computer simulations, and theory, the structure and other thermodynamical properties of organic suspensions of colloidal spheres, confined to a two-dimensional (2D) monolayer. Our studies reveal the effects of the dipolar interactions on the structure and the osmotic pressure of these fluids. These observations have far-reaching consequences for the fundamental colloidal science, opening new directions in self-assembly of complex colloidal clusters

Mechanical properties of colloidal crystals at fluid interfaces

We characterise the local mechanical properties of two-dimensional colloidal crystals with hexagonal symmetry assembled at the flat interface between oil and water. Our experiments elucidate the conditions under which the material behaves isotropically, as opposed to those where the microstructure plays a major role. Brownian fluctuations are used to extract the stiffness of the lattice under the continuum approximation, whereas at larger displacements, obtained by optically driving one particle through the structure, the mechanical resistance of the lattice depends on both the area fraction and the direction of the applied force. Remarkably, the minimum resistance does not necessarily correspond to a probe being driven between neighbours, i.e. at 30° with respect to the crystal axes

Hierarchical self-assembly of polydisperse colloidal bananas into a two-dimensional vortex phase

Self-assembly of microscopic building blocks into highly ordered and functional structures is ubiquitous in nature and found at all length scales. Hierarchical structures formed by colloidal building blocks are typically assembled from monodisperse particles interacting via engineered directional interactions. Here, we show that polydisperse colloidal bananas self-assemble into a complex and hierarchical quasi–two-dimensional structure, called the vortex phase, only due to excluded volume interactions and polydispersity in the particle curvature. Using confocal microscopy, we uncover the remarkable formation mechanism of the vortex phase and characterize its exotic structure and dynamics at the single-particle level. These results demonstrate that hierarchical self-assembly of complex materials can be solely driven by entropy and shape polydispersity of the constituting particles

Anomalous grain growth in a polycrystalline monolayer of colloidal hard spheres

Understanding grain growth is key for controlling the microstructure and the mechanical properties of most polycrystalline materials, including metals, alloys and ceramics. However, the precise mechanisms and kinetics of grain growth remain poorly understood both at the theoretical level and experimentally as direct observation is cumbersome in atomic systems. Here, we study the grain growth process in a polycrystalline monolayer of colloidal hard spheres. We find that the bond-orientational correlation function satisfiees the dynamic scaling hypothesis and has the general scaling form predicted for systems containing random domain walls. However, the associated correlation length grows slower than ~ t^1/2 that corresponds to normal curvature-driven grain growth. To understand the origin of this anomalous grain growth, we directly monitor the evolution of the grain boundary network by measuring the so-called grain boundary character distribution. We show that there is a strong annihilation of large angle grain boundaries while small angle grain boundaries become relatively more present. Using scaling arguments, we derive the time dependence of the correlation length and show its good agreement with the data. We conclude that the origin of anomalous grain growth is the curvature-driven coarsening of the large angle grain boundaries at a rate which depends on their relative length in the total grain boundary network

Colloidal crystal-fluid interfaces

In this article we show that colloidal systems are excellent model systems to experimentally study crystal-fluid interfaces. Using confocal microscopy it is possible to investigate static and dynamic interfacial properties in three dimensions and on the single particle level. The combination of real-space microscopy and colloidal model systems may provide a possible route to directly access the anisotropic interfacial free energy and the kinetic growth coefficient of crystal-fluid interfaces

Visitors

Health Display in the Outpatients area next to the Pharmacy in the main foyer, some of the groups include Red Cross, Drug and Alcohol services, Hillcresr hospital, Arthritis Foundation and many others.Photo size - 12.5 x 19cm,stored: record folder 2 & Negative Folder: 11.2 Community Health [1