Published in

Oldenbourg Verlag, Radiochimica Acta, 7(88), p. 425-430, 2000

DOI: 10.1524/ract.2000.88.7.425

Links

Tools

Export citation

Search in Google Scholar

The oxidation of hydroxylamine by nitric and nitrous acids in the presence of technetium (VII)

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

Full text: Unavailable

Green circle
Preprint: archiving allowed
Orange circle
Postprint: archiving restricted
Orange circle
Published version: archiving restricted
Data provided by SHERPA/RoMEO

Abstract

The oxidation of hydroxylamine by nitric acid in the presence of technetium ions at temperatures above ~60°C is an autocatalytic process comprising an induction period and then a catalysed reaction involving HNO2, which has accumulated in the solution. Tc ions have no appreciable effect on the reaction rate, which is governed only by the nitric and nitrous acid oxidation reactions of hydroxylamine, but the presence of Tc ions does extend the initial induction period. The rate of hydroxylamine oxidation by HNO3in the presence of HNO2, that is, after the induction period, was found to be:-d[NH3OH+]/dt = k[NH3OH+][HNO2][HNO3]3.5where k = 120±10 l4.5mol-4.5min-1at T = 80°C, μ = 2 and [H+] ≤ 2 M. Under these conditions, the reaction apparently has a high activation energy of 160-180 kJ mol-1. At low temperatures (20-40°C) hydroxylamine is effectively stable in solutions of HNO3up to concentrations of ~2 M, whether or not Tc(VII) ions are present. Tc(V) was also observed to form at least one complex on reduction with excess hydroxylamine with an absorption maximum between 467 and 480 nm dependent on the solution acidity.