Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/15765
Title: Mechanism of oxidation of ethanolamines by sodium N-chloro-p-toluenesulphonamide in alkaline buffer medium: A kinetic study
Authors: Mayanna, S M
Puttaswamy
Madhumathy, S
Issue Date: Jun-1999
Publisher: NISCAIR-CSIR, India
Abstract: Kinetics of oxidation of monoethanolamine (MEA), diethanolamine (DEA) and triethanolamine (TEA) by sodium Nchloro- p-toluenesulphonamide (chloramine-T, CAT) in alkaline buffer medium has been studied at 313K. The reactions followed identical kinetics being first order in [CAT] and fractional order each in [substrate] and [OH-]. Under comparable experimental conditions the rate of oxidation increases in the order: DEA > TEA > MEA. Addition of the reaction product p-toluenesulphonamide retards the reaction rate. Added chloride ions and change in ionic strength of the medium do not have any effect on the rate of the reaction . Change in dielectric constant of the medium affects the reaction rate. Activation parameters for the rate determining step are evaluated and isokinetic relation is observed with β=390 K indicating that the reactions are enthalpy-controlled. Formation and decomposition constants of substrate - CAT complexes are evaluated. Suitable mechanisms and rate equations are proposed based on the observed kinetic data.
Page(s): 547-552
Appears in Collections:IJC-A Vol.38A(06) [June 1999]

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