
Chemosphere p. 2637 - 2648 (1997)
Update date:2022-08-11
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The dark degradation of tetraacetylethylenediamine (TAED) was investigated, It is a slow process which is favored in acidic medium, There is a hydrolysis of an imide group with the scission of the C-N bond giving rise to the triacetyl derivative (TAED'). When allowed to stand for longer times a second acetyl group is eliminated with the formation of the symetric diacetyl derivative (DAED). The degradation of TAED photoinduced by iron (m) was also investigated. It appears a faster degradation which does not lead to the same products. The process only involves 'OH radicals formed upon photolysis of aquocomplex of iron (III). They preferentially abstract a hydrogen from the methylene group. The degradation is then assisted by oxygen and leads to the formation of carbonylated oxidation products.
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Doi:10.1007/BF00567923
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