Kinetic Micellar Effects in Tetradecyltrimethylammonium Bromide–Pentanol Micellar Solutions

✍ Scribed by Amalia Rodrı́guez; Marı́a Múñoz; Marı́a del Mar Graciani; Marı́a Luisa Moyá

• Publisher: Elsevier Science
• Year: 2002
• Tongue: English
• Weight: 154 KB
• Volume: 248
• Category: Article
• ISSN: 0021-9797
• DOI: 10.1006/jcis.2002.8215

✦ Synopsis

The reactions 1,1,1-trichloro-2,2-bis(p-chlorophenyl)ethane + OH(-) and 2-(p-nitrophenyl)ethyl bromide + OH(-) were studied in tetradecyltrimethylamonium bromide, TTAB, and TTAB-pentanol micellar solutions. The influence of changes in the surfactant concentration as well as changes in the hydroxide ion concentration on the observed rate constant was investigated. If changes in the cmc and ionization degree provoked by the presence of the different amounts of n-pentanol in the micellar solutions are taken into account, the experimental kinetic data can be rationalized quantitatively by using the PIE model. Assuming that the ion-exchange equilibrium constant, K(OH(-)/Br(-)), for the competition between the bromide and the hydroxide ions in all TTAB and in TTAB-pentanol micellar solutions studied is the same, a good agreement between the theoretical and the experimental kinetic data was found in all the micellar media for the two processes studied. This assumption was checked by experimentally determining the ion-exchange equilibrium constant K(OH(-)/Br(-)) in TTAB and TTAB-pentanol micellar solutions through a spectroscopic method, results showing that the presence of n-pentanol does not affect substantially the value of K(OH(-)/Br(-)). The second-order rate constants obtained from the fittings decrease slightly when the amount of pentanol increases, being greater than that in aqueous solution. This acceleration can be explained considering that micelles accelerate the reactions in which the charge is delocalized in the transition state.