Heterogeneous single-step flow reaction

Scheme 7.1 Typical arrangements for a heterogeneous single-step flow reaction.

The basic problem in the design of a heterogeneous reactor is to determine the quantity of catalyst and/or reactor size required for a given conversion and flow rate. In order to obtain this, information on the rate equaiion(s) and their parameter(s) must be made available. A rigorous approach to the evaluation of reaction velocity constants has yet to be accomplished for catalytic reactions at this time, industry still relies on the procedures set forth in the previous chapter. For example, in catalytic combustion leac-tioas, the rate equation is extremely complex and cannot be obtained either analytically or numerically. A number of equations may result and some simplification is often warranted. As mentioned earlier, in many cases it is safe to assume that the expression may be satisfactorily expressed by the rate equation of a single step. 

The first equation represents the equilibrium between hydrated Ag+ ions and Ag atoms in a single-crystal configuration. Alternatively, we may say that there is a heterogeneous thermodynamic equilibrium between Ag+ ions in the solid phase (where they are stabilized by the gas of free electrons) and Ag+ ions in the liquid phase (stabilized by interaction with water molecules). The forward reaction step corresponds to the anodic dissolution of a silver crystal. On an atomic level, one may say that a Ag" " core ion is transferred from the metallic phase to the liquid water phase. In an electrochemical cell, an electron flows from the Ag electrode (the working electrode) to the counter electrode each time that one Ag+ ion is transferred from the solid to the liquid phase across the electrochemical double layer. Although the electron flow is measured in the external circuit between the working... 

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