Colloidal dispersions particle size, effect

Arroyo, F.J., Carrique, F., Bellini, T., and Delgado, A.V., Dielectric dispersion of coUoidal suspensions in the presence of Stem layer conductance particle size effects, J. Colloid Interface Sci., 210, 194, 1999. 

Akashi and coworkers prepared small platinum nanoparticles by ethanol reduction of PtCl in the presence of various vinyl polymers with amide side chains [49]. These authors studied the effects of molecular weight and molar ratio [monomeric unit]/[Pt] on the particle sizes and size distributions by electron microscopy, and in some cases by the dispersion stability of the Pt colloids. The hydrogenation in aqueous phase of allyl alcohol was used as a model reaction to examine the change in catalytic activity of polymer-stabilized Pt colloids upon addition of Na2S04 to the reaction solution. The catalytic tests were performed in water or in Na2S04 aqueous solution at 25 °C under atmospheric pressure of... 

Kreuter and Speiser [77] developed a dispersion polymerization producing adjuvant nanospheres of polymethylmethacrylate) (PMMA). The monomer is dissolved in phosphate buffered saline and initiated by gamma radiation in the presence and absence of influenza virions. These systems showed enhanced adjuvant effect over aluminum hydroxide and prolonged antibody response. PMMA particles could be distinguished by TEM studies and the particle size was reported elsewhere to be 130 nm by photon correlation spectroscopy [75], The particle size could be reduced, producing monodisperse particles by inclusion of protective colloids, such as proteins or casein [40], Poly(methylmethacrylate) nanoparticles are also prepared... 

Microstructures of CLs vary depending on applicable solvenf, particle sizes of primary carbon powders, ionomer cluster size, temperafure, wetting properties of carbon materials, and composition of the CL ink. These factors determine the complex interactions between Pt/carbon particles, ionomer molecules, and solvent molecules, which control the catalyst layer formation process. The choice of a dispersion medium determines whefher fhe ionomer is to be found in solubilized, colloidal, or precipitated forms. This influences fhe microsfrucfure and fhe pore size disfribution of the CL. i It is vital to understand the conditions under which the ionomer is able to penetrate into primary pores inside agglomerates. Another challenge is to characterize the structure of the ionomer phase in the secondary void spaces between agglomerates and obtain the effective proton conductivity of the layer. 

Two classes of grinding equipment are used to prepare dispersions. The first, the colloid mill, does not effect a particle size reduction but does break down aggregates of fine particles. Colloid mills are used for such powders as clays, precipitated whiting, etc. Sometimes these mills are used to process zinc oxide but for dipped mbber products that is not satisfactory. 

Although they are a relatively small volume product—approximately 75,000 tons produced in 1949 (126)—interest in asphalt emulsion has continued at a high level. Abraham (6) has reviewed the patent literature relative to the types of emulsifying agents used, while commercial practice has been discussed by Day (16). The most common emulsifiers are sodium or potassium soaps of tall oil, abietic acid, or Vinsol resin, or colloidal clays such as bentonite for adhesive base emulsions. Lyttleton and Traxler (53) studied the flow properties of asphalt emulsions, and Traxler (122) has investigated the effect of size distribution of the dispersed particles on emulsion viscosity. A decrease in particle size uniformity was found to be accompanied by a decrease in consistency because particles of various size assume a more loosely packed condition than do those of the same size. 

Polyacrylic acid stabilised latices have been prepared by aqueous dispersion polymerisation. The method used is analogous to the non-aqueous dispersion (NAD) polymerisation methods originally used to prepare polymethyl methacrylate particles in aliphatic hydrocarbons (1. In effect the components of a NAD polymerisation have been replaced as follows aliphatic hydrocarbon by aqueous alcohol, and degraded rubber, the stabiliser, by polyacrylic acid (PAA). The effect of various parameters on the particle size and surface charge density of the latices is described together with details of their colloidal stability in the presence of added electrolyte. 

The most important factor influencing the degree of steric stabilization is the thickness of the adsorbed layer in comparison with the size of the particles [292], The term protection has also been used because the steric stabilizing effect can cause significant salt tolerance on the part of a colloidal dispersion. Some suspensions have been prepared, using high concentrations of polyelectrolytes, that are quite stable in concentrated salt solutions [49]. 

Applications of optical methods to study dilute colloidal dispersions subject to flow were pioneered by Mason and coworkers. These authors used simple turbidity measurements to follow the orientation dynamics of ellipsoidal particles during transient shear flow experiments [175,176], In addition, the superposition of shear and electric fields were studied. The goal of this work was to verify the predictions of theories predicting the orientation distributions of prolate and oblate particles, such as that discussed in section 7.2.I.2. This simple technique clearly demonstrated the phenomena of particle rotations within Jeffery orbits, as well as the effects of Brownian motion and particle size distributions. The method employed a parallel plate flow cell with the light sent down the velocity gradient axis. 

Particles can be broadly classified as either colloids or as macroparticulate powders. Colloids typically have dimensions smaller than 1000 A and are optically transparent, while dispersed powders are generally larger and form turbid suspensions. Neither colloidal dispersions nor powder suspensions are usually monodisperse, and to the extent that particle size can influence attainable surface charge and area, many such systems will typically reflect a distribution of properties as a function of preparation method. Recent advances in synthetic techniques for providing materials with reduced polydispersity are likely to allow for better characterization of these effects in the near future. 

Most food systems are of a colloidal as well as a polymeric nature. The presence of a nonadsorbing polymer in a skim milk dispersion induces an effective attraction between the casein particles, called depletion interaction, resulting in phase separation at sufficiently high polymer concentration. Tuinier et al. (2003) discussed the influence of colloid-polymer size ratio, polymer concentration regime, size, poly-dispersity and charges in colloid/biopolymer mixtures, demonstrating the challenging complexity of the subject. 

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