Kinetics and equilibria in the nitric acid–nitrous acid–sodium thiocyanate system
Eleanor Jones, Carl G. Munkley, Evan D. Phillips, Geoffrey E. Stedman
Abstract
Eleanor Jones, Carl G. Munkley, Evan D. Phillips, Geoffrey E. Stedman
Abstract
The nature of the red species formed in acidic solutions containing nitrous acid and thiocyanate ion has been confirmed to be ONSCN. The alternative literature interpretation in terms of ONSCNH+ arises from neglect of activity coefficients and partial protonation of SCN– to HNCS in moderately concentrated mineral acid. The kinetics of the nitrous acid-catalysed oxidation of thiocyanate in moderately concentrated nitric acid is controlled by rate-determining formation of N2O4 at even modest concentrations of thiocyanate. Literature work on this system is discussed.
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The nature of the red species formed in acidic solutions containing nitrous acid and thiocyanate ion has been confirmed to be ONSCN. The alternative literature interpretation in terms of ONSCNH+ arises from neglect of activity coefficients and partial protonation of SCN– to HNCS in moderately concentrated mineral acid. The kinetics of the nitrous acid-catalysed oxidation of thiocyanate in moderately concentrated nitric acid is controlled by rate-determining formation of N2O4 at even modest concentrations of thiocyanate. Literature work on this system is discussed.
Key concepts: Nitrous acid, Thiocyanate, Chemistry, Nitric acid, Sodium thiocyanate, Inorganic chemistry, Kinetics, Protonation