Kinetics and mechanism of cetyltrimethylammonium bromide catalyzed oxidation of diethylene glycol by chloramine-T in acidic medium

The kinetics and mechanism of the C16TABcatalyzed oxidation of diethylene glycol (2,2?-oxydiethanol) by chloramine-T in acidic medium has been studied. The reaction has a first-order dependence on chloramine-T. With excess concentrations of other reactants, the reaction rate follows fractional order...

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Veröffentlicht in:Journal of the Serbian Chemical Society 2003, Vol.68 (7), p.535-542
Hauptverfasser: Bhagwat, V.W., Tiwari, J., Choube, A., Pare, B.
Format: Artikel
Sprache:eng
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Zusammenfassung:The kinetics and mechanism of the C16TABcatalyzed oxidation of diethylene glycol (2,2?-oxydiethanol) by chloramine-T in acidic medium has been studied. The reaction has a first-order dependence on chloramine-T. With excess concentrations of other reactants, the reaction rate follows fractional order kinetics with respect to [diethylene glycol]. The micellar effect due to cetyltrimethylammonium bromide, a cationic surfactant, has been studied. The reaction is catalyzed by chloride ions as well. The small salt effect and increase in the reaction rate with increasing dielectric constant suggest the involvement of neutral molecules in the rate determining step. Addition of p-toluenesulfonamide retards the reaction rate. On the basis of product analysis, a pertinent mechanism is proposed. Proucavana je oksidacija dietilen-glikola(2,2?-oksidietanol) hloraminom-T koja je katalizovana pomocu C16TAB u kiseloj sredini. Reakcija je prvog reda u odnosu na hloramin-T. U visku koncentracija drugih reaktanata red reakcije u odnosu na dietilen-glikol je razlomljen. Proucavan je i micelarni efekat cetiltrimetil-amonijum-bromida, koji je katjonska povrsinski aktivna supstanca. Reakciju takodje katalizuju i hloridni joni. Mali soni efekat i povecanje brzine reakcije povecanjem dielektricne konstante ukazuje na ucestvovanje neutralnih molekula u sporom stupnju reakcije. Dodavanje p-toluensulfonamida usporava reakciju. Na osnovu rezultata predlozen je odgovarajuci mehanizam reakcije.
ISSN:0352-5139
1820-7421
DOI:10.2298/JSC0307535B