The kinetics and mechanism of reduction of aqueous toluidine blue by ϩ (TB ) phenyl hydrazine (Pz), which exhibits nonlinear behavior, is studied spectrophotometrically at Typical kinetic curves exhibited autocatalytic characteristics. The role of as an ϩ 630 nm. H autocatalyst is established. Rate
Kinetics and mechanism of reaction of toluidine blue with acidic bromate
✍ Scribed by S. B. Jonnalagadda; N. Musengiwa
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 209 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0538-8066
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✦ Synopsis
The detailed kinetics of the reaction of toluidine blue {phenothiazine-5-ium, 3amino-7(dimethylamino)-2-methyl chloride, tolonium chloride, with potassium bro-ϩ Ϫ TB Cl } mate and with aqueous bromine reaction were studied. In most of the experiments, the kinetics were monitored by following the rate of consumption of at with excess acid ϩ TB 590 nm and bromate. The reaction exhibited complex kinetic behavior. Initial reaction was slow and after an induction time, the concentration decreased fast. It had first-order dependence ϩ TB on both and bromate, and second-order dependence on Under excess bromate con-ϩ ϩ TB H . ditions, the stoichiometric ratio of to bromate was Demethylated sulfoxides were ϩ TB 1 : 1. found at the reaction products. Sharp increase in the overall potential synchronized with the increase in bromine levels and the fast depletion of The role of bromide ion and bromine ϩ [TB ]. in the reaction was established. A multi-step reaction mechanism is proposed consistent with the experimental results.
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