In situ imaging technology developed for nuclear medicine is now being
applied to study the kinetics of heterogeneous catalytic reactions un
der actual process conditions. Minute quantities of molecules (ca. 10-
(15) mel), radio-labeled with positron-emitting isotopes such as C-11;
N-13; or O-15, are injected as pulses into the feed streams of chemica
l reactors. Subsequent coincident detection of pairs of gamma photons
produced via positron-electron annihilation allows the concentration o
f reactants, intermediates and products to be mapped as a function of
both time and position within the reactor bed. As well as providing qu
alitative information regarding the mechanism of the reaction under in
vestigation the data obtained can be compared with mathematical models
based on the reaction kinetics in order to refine parameters such as
activation energies and pre-exponential factors for elementary reactio
n steps. Since the technique is capable of imaging transient phenomena
, information is provided that is not accessible to steady-state techn
iques.