In this paper, we examine the wet-air oxidation (WAO) of four nuclear-fuel-
chelating compounds [diethylenetriaminepentaacetic acid (DTPA), ethylenedia
minetetraacetic acid (EDTA), nitrilotriacetic acid (NTA), and thenoyltriflu
oroacetone (TTA)]. The study focuses on the kinetics and mechanism of the d
egradation process. Identification of the free-radical intermediates was pe
rformed via the spin-trapping technique. The reaction of each compound stud
ied was found to occur in two steps, with a partial order of one with respe
ct to TOC for both steps. Among the compounds studied,TTA shows the most di
fficulty when degrading. Hydroxyl, hydroxycarbonyl, and nitrogenous radical
s are some of those formed during the degradation process. Schematic reacti
on pathways, which can explain the formation of some mineral byproducts, ar
e proposed an the basis of these radicals.