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The hydrolysis of hydroxamic acid complexants in the presence of non-oxidizing metal ions 1: Ferric ions.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

<mark>Journal publication date</mark>10/2007
<mark>Journal</mark>Journal of Solution Chemistry
Issue number10
Number of pages17
Pages (from-to)1201-1217
Publication StatusPublished
<mark>Original language</mark>English


Hydroxamic acids (XHAs) are organic compounds with affinities for cations such as Fe3+, Np4+ and Pu4+ and have been identified as useful reagents in nuclear fuel reprocessing. Acid catalyzed hydrolysis of free XHAs is well known and may impact negatively on reprocessing applications. The hydrolysis of metal-bound XHAs within metal ion-XHA complexes is less understood. With the aid of speciation diagrams, we have modelled UV-visible spectrophotometric kinetic studies of the acid-catalyzed hydrolysis of acetohydroxamic acid (AHA) bound to the model ion Fe(III). These studies have yielded the following information for the hydrolysis of AHA in the Fe(AHA)2+ complex at 293 K: (i) the order with respect to [H+] during the rate determining step, m=0.97, is the same as for the free ligand, indicating a similarity of mechanisms; and (ii) the kinetic rate parameter, k 1=1.02×10−4 dm3⋅mol−1⋅s−1, is greater than that for the free ligand, k 0=1.84×10−5 dm3⋅mol−1⋅s−1 for pH>−0.5, a result that is consistent with a Hammett analysis of the system.

Bibliographic note

The original publication is available at www.springerlink.com