Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Colloidal systems surface preparation

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. [Pg.283]

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). [Pg.49]

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]. [Pg.96]

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. [Pg.5]

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... [Pg.89]

The question of surface preparation in colloidal systems takes the form of colloid preparation and stability. Several questions are of interest ... [Pg.282]

We have chosen hematite oxalate as a model system, since the photochemical properties of colloidal hematite (Stramel and Thomas, 1986) and the photochemistry of iron(III) oxalato complexes in solution (Parker and Hatchard, 1959) have been studied extensively. The experiments presented in this section were carried out as batch experiments with monodispersed suspensions of hematite (diameter of the particles 50 and 100 nm), synthesized according to Penners and Koopal (1986) and checked by electron microscopy and X-ray diffraction. An experimental technique developed for the study of photoredox reactions with colloidal systems (Sulzberger, 1983) has been used. A pH of 3 was chosen to maximize the adsorption of oxalate at the hematite surface. This case study is described in detail by Siffert (1989) and Siffert et al. (manuscript in preparation). [Pg.413]

In some cases under the conditions similar to those corresponding to the formation of lyophilic colloidal systems, a spontaneous formation of emulsions, the so-called self-emulsification, may take place. This is possible e.g. when two substances, each of which is soluble in one of the contacting phases, react at the interface to form a highly surface active compound. The adsorption of the formed substance under such highly non-equilibrium conditions may lead to a sharp decrease in the surface tension and spontaneous dispersion (see, Chapter III, 3), as was shown by A.A. Zhukhovitsky [42,43], After the surface active substance has formed, its adsorption decreases as the system reaches equilibrium conditions. The surface tension may then again rise above the critical value, acr. Similar process of emulsification, which is an effective method for preparation of stable emulsions, may take place if a surfactant soluble in both dispersion medium and dispersed liquid is present. If solution of such a surfactant in the dispersion medium is intensively mixed with pure dispersion medium, the transfer of surfactant across the low surface tension interface occurs (Fig. VIII-10). This causes turbulization of interface... [Pg.610]

For most biological studies, the ICPs have been prepared in the form of a flat film although some tubular structures have also been prepared. An evolving area of interest is the synthesis of high surface area bioactive colloidal systems [32]. PPy-polystyrene core latex particles with an inner core 600 nm in diameter have been functionalized with N-succinimidyl ester [33,34] and AT-hydroxysuccinimide [35] to introduce protein-binding capacity. Functionalization of these particles exhibited a high degree of... [Pg.1462]


See other pages where Colloidal systems surface preparation is mentioned: [Pg.13]    [Pg.39]    [Pg.180]    [Pg.267]    [Pg.255]    [Pg.198]    [Pg.681]    [Pg.239]    [Pg.39]    [Pg.188]    [Pg.402]    [Pg.28]    [Pg.665]    [Pg.1347]    [Pg.291]    [Pg.495]    [Pg.161]    [Pg.195]    [Pg.560]    [Pg.282]    [Pg.120]    [Pg.104]    [Pg.624]    [Pg.755]    [Pg.16]    [Pg.42]    [Pg.195]    [Pg.924]    [Pg.225]    [Pg.450]    [Pg.39]    [Pg.85]    [Pg.73]    [Pg.248]    [Pg.224]    [Pg.134]    [Pg.83]    [Pg.176]    [Pg.267]    [Pg.325]   
See also in sourсe #XX -- [ Pg.282 ]




SEARCH



Colloid surfaces

Colloidal surfaces

Colloidal systems

Colloidal systems preparation

Colloids preparation

Surface preparation

System preparation

© 2024 chempedia.info