Colloidal systems preparation

Table 1. SAXS results of Si02 colloid systems prepared under various conditions. ...

In the same way, ruthenium colloidal systems prepared by reduction of RuCh under dihydrogen in the presence of trioctylamine allowed reduction of various substituted aromatics [27]. They studied the stereo- and chemo-selectivities of the hydrogenation of aromatics in a methanol-water system at 50 bar of H2 and at room temperature. The results obtained are presented in Table 11.5. Reaction time to reach 100% conversion depends on the electronic and steric properties of the substituents on the aromatic ring, more electron-rich substrates giving rise to a favored reaction. 

The emphases of future investigation on these unprotected metal nanoclusters should be mainly placed on (1) further controlling the size, composition and shape of the unprotected metal or alloy nanoclusters (2) better understanding the stabilizing mechanism of the unprotected metal nanoclusters in colloidal solutions prepared by the alkaline EG synthesis method (3) developing novel catalytic and other functional systems for real applications. 

The interfacial properties of chain-like molecules in many polymeric and colloidal systems are dependent on the conformation of the chains adsorbed at the interface (.1). Chains adsorbed at the solid-liquid interface may be produced by anchoring diblock copolymers to particles in a polymer dispersion. Such dispersions are conveniently prepared by polymerizing in the presence of a preformed AB diblock copolymer a monomer dissolved in a diluent which is a precipitant for the polymer. The A block which is... 

Similar surfactant-stabilized colloidal systems have been reported by Albach and Jautelat, who prepared aqueous suspensions of Ru, Rh, Pd, Ni nanoparticles and bimetallic mixtures stabilized by dodecyldimethylammonium propane-sulfonate [103]. Benzene, cumene and isopropylbenzene were reduced in biphasic conditions under various conditions at 100-150 °C and 60 bar H2, and TTO up to 250 were obtained. 

In 1996, Liu et al. reported the selective hydrogenation of cinnamaldehyde, an a,/ -unsaturated aldehyde, to cinnamyl alcohol, an a,/ -unsaturated alcohol, by means of PVP-protected Pt/Co bimetallic colloids prepared by the polyol process [111]. The colloids were obtained as a dark-brown homogeneous dispersion in a mixture of ethylene glycol and diethylene glycol, and characterized by TEM and XRD. These authors prepared different samples of nanoparticles with Pt Co ratios of 3 1 and 1 1, the mean diameters of which measured 1.7 and 2.2 nm, respectively. These colloidal systems were also compared with the single metal-... 

In order to evaluate the catalytic characteristics of colloidal platinum, a comparison of the efficiency of Pt nanoparticles in the quasi-homogeneous reaction shown in Equation 3.7, with that of supported colloids of the same charge and of a conventional heterogeneous platinum catalyst was performed. The quasi-homogeneous colloidal system surpassed the conventional catalyst in turnover frequency by a factor of 3 [157], Enantioselectivity of the reaction (Equation 3.7) in the presence of polyvinyl-pyrrolidone as stabilizer has been studied by Bradley et al. [158,159], who observed that the presence of HC1 in as-prepared cinchona alkaloids modified Pt sols had a marked effect on the rate and reproducibility [158], Removal of HC1 by dialysis improved the performance of the catalysts in both rate and reproducibility. These purified colloidal catalysts can serve as reliable... 

A colloidal suspension prepared according to the method described in Section 13.2.3 was contacted with a porous alumina carrier to obtain a bimetallic palladium-tin catalyst. Evaluation of the catalytic properties of this system is detailed... 

The procedure chosen for the preparation of lipid complexes of AmB was nanoprecipitation. This procedure has been developed in our laboratory for a number of years and can be applied to the formulation of a number of different colloidal systems liposomes, microemulsions, polymeric nanoparticles (nanospheres and nanocapsules), complexes, and pure drug particles (14-16). Briefly, the substances of interest are dissolved in a solvent A and this solution is poured into a nonsolvent B of the substance that is miscible with the solvent A. As the solvent diffuses, the dissolved material is stranded as small particles, typically 100 to 400 nm in diameter. The solvent is usually an alcohol, acetone, or tetrahydrofuran and the nonsolvent A is usually water or aqueous buffer, with or without a hydrophilic surfactant to improve colloid stability after formation. Solvent A can be removed by evaporation under vacuum, which can also be used to concentrate the suspension. The concentration of the substance of interest in the organic solvent and the proportions of the two solvents are the main parameters influencing the final size of the particles. For liposomes, this method is similar to the ethanol injection technique proposed by Batzii and Korn in 1973 (17), which is however limited to 40 mM of lipids in ethanol and 10% of ethanol in final aqueous suspension. 

The major disadvantages of colloidal catalysts studied so far can be attributed to problems in controlling the metal colloid formation (control of particle size, particle size distribution, structure of metal colloids) and stabilization of the prepared particles, which are not yet completely solved. But it is exactly the stability of the nanoparticles, that is decisive for long-term usage during catalytic processes. Moreover for catalytic application, it is extremely important to preserve the large surface of such colloidal systems. 

Despite their catalytic (preparative) efficiency similar colloidal systems will be only occasionally included into the present description of aqueous organometalHc catalysis although it should be kept in mind that in aqueous systems they can be formed easily. Catalysis by colloids is a fast growing, important field in its own right, and special interest is turned recently to nanosized colloidal catalysts [62-64]. This, however, is outside the scope of this book. 

N. Uson, MJ. Garcia, and C. Solans Formation of Water-in-Oil (W/O) Nano-Emulsions in a Water/Mixed Non-Ionic Surfactant/Oil Systems Prepared by a Low-Energy Emulsification Method. Colloid and Surfaces A Physicochem. Eng. Aspects 250, 415 (2004). 

Monodisperse spheres are not only uniquely easy to characterize, but also very rarely encountered. Polymerization under carefully controlled conditions allows the preparation of the polystyrene latex shown in Figure 1.8. Latexes of this sort are used as standards for the size calibration of optical and electron micrographs (also see Section 1.5a.3). However, in the majority of colloidal systems, the particles are neither spherical nor monodisperse, but it is often useful to define convenient effective linear dimensions that are representative of the sizes and shapes of the particles. There are many ways of doing this, and whether they are appropriate or not depends on the use of such dimensions in practice. There are excellent books devoted to this topic (see, for example, Allen 1990) and, therefore, we consider only a few examples here for the purpose of illustration. 

Another colloidal system with light scattering characteristics that have been widely studied is the so-called monodisperse sulfur sol. Although not actually monodisperse, the particle size distribution in this preparation is narrow enough to make it an ideal system for the study of optical phenomena. 

Accordingly, in the earlier exercises, 23 in number, attention is centered on methods of manipulation for overcoming the usual varieties of difficulties and in gaining experience in the use of preparative processes. Later exercises are arranged with reference to a number of types of compounds and the reactions available for their preparation. A final group of exercises is provided to illustrate the chief characteristics of colloidal systems. 

For the preparation of suspensions and emulsions, colloid mills and liuiiiogeiiizers, respectively, are used. Ultrasonic mills that utilize vibrating reeds in restricted chambers to reduce the particle size of the dispersed ingredients can also be employed. See also Colloid Systems. 

Special probes were introduced to measure surface forces in colloidal systems as a function of the ionic strength and the concentration of surfactant molecules [214]. A so-called colloid probe can be prepared by gluing a silica sphere onto a conventional Si3N4 tip [179]. 

The surface or interfacial phenomena associated with colloidal systems such as emulsions and foams are often studied by means of experiments on artificially prepared flat surfaces rather than on the colloidal systems themselves. Such methods provide a most useful indirect approach to the various problems involved. 

Any machine for preparing colloidal systems by dispersion. Examples colloid mill, blender, ultrasonic probe. See Airless Spraying. 

Emulsions and suspensions are colloidal dispersions of two or more immiscible phases in which one phase (disperse or internal phase) is dispersed as droplets or particles into another phase (continuous or dispersant phase). Therefore, various types of colloidal systems can be obtained. For example, oil/water and water /oil single emulsions can be prepared, as well as so-called multiple emulsions, which involve the preliminary emulsification of two phases (e.g., w/o or o/w), followed by secondary emulsification into a third phase leading to a three-phase mixture, such as w/o/w or o/w/o. Suspensions where a solid phase is dispersed into a liquid phase can also be obtained. In this case, solid particles can be (i) microspheres, for example, spherical particles composed of various natural and synthetic materials with diameters in the micrometer range solid lipid microspheres, albumin microspheres, polymer microspheres and (ii) capsules, for example, small, coated particles loaded with a solid, a liquid, a solid-liquid dispersion or solid-gas dispersion. Aerosols, where the internal phase is constituted by a solid or a liquid phase dispersed in air as a continuous phase, represent another type of colloidal system. 

The electrical double layer interaction is a key feature of a great many colloidal systems that are of technological significance. In the preparation and useful shelf-life of paints, and/or inks, or in the area of detergency where the properties of charged surface active compounds come into consideration the stabilizing influence of the edl interaction is important. Special mention... 

The applications of colloid solutions are not restricted to paints and clay. They are also to be found in inks, mineral suspensions, pulp and paper making, pharmaceuticals, cosmetic preparations, photographic films, foams, soaps, micelles, polymer solutions and in many biological systems, for example within the cell. Many food products can be considered colloidal systems. For example, milk is an interesting mixture containing over 100 proteins, mainly large casein and whey proteins [6,7]. 

Several methods have been developed for preparing nanoparticles and are optimized on the basis of their physicochemical properties (e.g., size and hy-drophilicity) with regard to their in vivo fate after parenteral administration. The selection of the appropriate method for preparing drug-loaded nanoparticles depends on the physicochemical properties of the polymer and the drug. On the other hand, the procedure and the formulation conditions will determine the inner structure of these polymeric colloidal systems. Two types of systems with different inner structures are possible ... 

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