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dc.contributor.authorMayanna, S M-
dc.contributor.authorPuttaswamy-
dc.contributor.authorMadhumathy, S-
dc.date.accessioned2013-01-18T17:02:42Z-
dc.date.available2013-01-18T17:02:42Z-
dc.date.issued1999-06-
dc.identifier.urihttp://hdl.handle.net/123456789/15765-
dc.description547-552en_US
dc.description.abstractKinetics 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.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.38A(06) [June 1999]en_US
dc.titleMechanism of oxidation of ethanolamines by sodium N-chloro-p-toluenesulphonamide in alkaline buffer medium: A kinetic studyen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.38A(06) [June 1999]

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