Premium
Kinetics of alkaline fading of methyl violet in micellar solutions of surfactants: Comparing Piszkiewicz's, Berezin's, and pseudophase ion‐exchange models
Author(s) -
Laguta An.,
Eltsov Sergey V.,
MchedlovPetrossyan Nikolay O.
Publication year - 2019
Publication title -
international journal of chemical kinetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.341
H-Index - 68
eISSN - 1097-4601
pISSN - 0538-8066
DOI - 10.1002/kin.21231
Subject(s) - chemistry , micelle , reaction rate constant , hydroxide , pulmonary surfactant , cationic polymerization , micellar solutions , bromide , kinetics , inorganic chemistry , aqueous solution , ion , photochemistry , organic chemistry , biochemistry , physics , quantum mechanics
The micellar effect of surfactants of various types on the rate of the reaction between methyl violet and hydroxide ion is studied. The absorption spectra show that the cation of methyl violet is bound by micelles of all types at proper concentrations of surfactants. The observed rate constant in micellar systems containing nonionic Brij‐35, zwitterionic 3‐(dimethyldodecylammonio)‐propanesulfonate, cationic cetyltrimethylammonium bromide and hydroxide surfactants is higher, whereas in solutions of the anionic surfactant sodium dodecylsulfate is lower than that one in the surfactant‐free system. Piszkiewicz's, Berezin's, and pseudophase ion‐exchange models of the kinetic micellar effect are used for the treatment of the dependences of the above‐mentioned constants on the surfactant concentration. The values of the corresponding kinetic parameters are compared and discussed. The influence of nonionic, zwitterionic, and anionic micelles on the reaction rate is discussed on the basis of medium and concentration kinetic effects. The character of the cationic micelles effect is somewhat paradoxical. Although the observed pseudo–first‐order reaction rate constant substantially increases in the presence of such micelles, the second order‐rate constant in these micelles is lower than the corresponding value in surfactant‐free aqueous solution. As a possible explanation, the decrease in the reactivity of the HO – ions is proposed, owing to their electrostatic association with the cationic headgroups (“diverting effect”).