Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/63023
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dc.contributor.authorSrivastava, Abhishek-
dc.contributor.authorGoswami, Madhav Krishna-
dc.contributor.authorSrivastava, Krishna-
dc.contributor.authorSrivastava, Neetu-
dc.date.accessioned2023-12-20T09:45:34Z-
dc.date.available2023-12-20T09:45:34Z-
dc.date.issued2023-12-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/63023-
dc.description1268-1275en_US
dc.description.abstractThe present study aims to explore the kinetics of Fe(II) catalyzed L-tryptophan (Trp) oxidation in micellar media by persulfate ion (S2O8 2–). The reaction's progress has been analyzed as an indicator of [S2O8 2–], temperature, [Trp], [Fe(II)], [Surfactant], ionic strength, and [H+]. The S2O8 2– undergoes a 1:1 stoichiometric interaction with Trp. The observed reaction exhibits first-order kinetics with regards to [S2O8 2–], fractional-first-order with respect to [H+], linear reliance to [Fe(II)], and invariance with respect to [Trp] within the range of concentrations investigated. The observed decrement in reaction rate upon electrolyte introduction is suggestive of a negative salt effect. The oxidation rate is significantly enhanced by Fe(II) solution (as a catalyst) at lower concentrations. Both the cationic cetyltrimethylammonium bromide (CTAB) and the anionic sodium dodecyl sulfate (SDS) have been shown to inhibit the oxidation rate, while the non-ionic Triton X-100 (TX-100) does not have a noticeable impact on the reaction rate.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.62(12) [December 2023]en_US
dc.subjectSurfactanten_US
dc.subjectMicelle encapsulationen_US
dc.subjectOxidationen_US
dc.subjectPersulfateen_US
dc.subjectIron(II) catalyzeden_US
dc.subjectL- Tryptophanen_US
dc.titleRole of surfactants on Fe(II) catalyzed L-tryptophan oxidation by persulfateen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v62i12.5608en_US
Appears in Collections:IJC Vol.62(12) [December 2023]

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