OH radical reactions with ethanolamine, diethanolamine and triethanolamine were studied at pH values below and above the pKa values of these compounds. The rate constants were found to be lower for the protonated amines than those for their neutral forms. The OH radical reaction led to the formation of both oxidizing, as well as reducing species, as observed by their reactions with methyl viologen and ascorbic acid. The oxidizing species formed by OH radical reaction at the amine site was not found to react with the parent molecules and thereby no secondary yield of reducing species was obtained, as in the case of glycine (except in the case of triethanolamine at pH 9.2).
Research on Chemical Intermediates – Springer Journals
Published: Nov 1, 2004
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