Abstract
Radiolytic G values were determined for Fe(II), iminodiacetic acid (IDA) and glyoxalic acid in deoxygenated aqueous solution of Fe(III)NTA, Fe(III)(NTA) 2 and Fe(III)(NTA) 3 and in the presence of scavengers O 2, N 2O, HCOO − and t-butanol. The mode of reaction of the radicals was found to be similar irrespective of number of NTA ligands around the metal ion. The metal ion was reduced directly by e −(aq), H or secondary radicals HO 2, O 2 −, CO 2 − and (CH 3) 2COH while the OH radical did so indirectly through alpha hydrogen abstraction from ligand followed by intramolecular electron transfer. The rate constants determined by competition kinetic methods at pH 6.0 were k[OH + Fe( III)NTA] = 2.5 x 10 8, k[OH + Fe( III)(NTA) 2] = 7.8 x 10 8, k[e −(aq) + Fe( III)NTA] = 3.0 x 10 10 and k[e −(aq) + Fe( III)(NTA) 2] = 2.1 x 10 10 dm 3 mol −1 s −1 and at pH 2.0, k[OH + Fe( III)(NTA) 2] = 6.4 x 10 8 dm 3 mol −1 s −1.
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