Composite dispersed materials Concentration dependence

As COR and OER occur simultaneously in the cathode, their kinetics are particularly important in evaluating carbon-support corrosion. The kinetics of OER is material-specific, dependent on catalyst composition and electrode fabrication.35,37 -39 A number of OER kinetics studies were done on Pt metal electrodes.37-39 However, there is a lack of OER kinetics data on electrodes made of Pt nano-particles dispersed on carbon supports. Figure 2 shows the measured OER current density with respect to the overpotential defined by Eq. (6).35 The 02 concentration was measured at the exit of a 50-cm2 cell using a gas chromatograph (GC). The 02 evolution rate (= 02 concentration x cathode flow rate) was then converted to the OER current density, assuming 4e /02 molecule. Diluted H2 (10%) and a thicker membrane (50 p,m) were used in the measurement to minimize H2 crossover from anode to cathode, because H2 would react with 02 evolved at the cathode and incur inaccuracy in the measured OER current density. Figure 2 indicates that the OER... 

This shape of the dependence d j.on the concentration of the initial disperse material is typical and is observed for other condition of aggregation, namely, the aggregation of graphite powder with the size of the initial particles 10 mcm in polymer composites, which is described by the empirical equation [21] ... 

In interfacial polymerization, monomers react at the interface of two immiscible liquid phases to produce a film that encapsulates the dispersed phase. The process involves an initial emulsification step in which an aqueous phase, containing a reactive monomer and a core material, is dispersed in a nonaqueous continuous phase. This is then followed by the addition of a second monomer to the continuous phase. Monomers in the two phases then diffuse and polymerize at the interface to form a thin film. The degree of polymerization depends on the concentration of monomers, the temperature of the system, and the composition of the liquid phases. 

Adsorption is the process of concentration of gases, vapours or liquids on the surface of pores of solid materials, as a result of adsorption forces. Two types of the adsorption forces may be considered — physical and chemical. When the substance adsorbed is bound to the surface of the adsorption agent by intermolecular forces (particularly dispersion forces), the adsorption is of a physical nature. Chemisorption occurs when these forces have the character of chemical interactions. The adsorption process depends on the temperature, pressure and chemical composition of the adsorbed gas and adsorbing material. The adsorption is always connected with a release of adsorption heat (and thus an appropriate level of cooling should be provided for large adsorption units). 

Nevertheless the use of dielectric materials obtained by conductive filler dispersion (carbon black, graphite fibres, metallic powders) is limited. As a matter of a fact material performances are dependent on the filler content as well as particle aggregation phenomena. These composites require a high level of reproducibility and their behaviour is linked to the control of electronic inter-particular transfer. The measured parameter (complex permittivity) depends on the texture of the percolation aggregates and consequently on the processing conditions. The percolation threshold (the particle concentration, after which particles are in contact and the electrical current exists) depends on the particle shape (sphere, plates or fibres). 

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