## Abstract The reaction Fe(CN)~4~(bpy)^2−^ + S~2~O~8~^2−^ has been studied in aqueous micellar solutions of __N__‐tetradecyl‐__N,N__‐dimethyl‐3‐ammonio‐1‐propanesulfonate, SB3‐14. The influence of changes in the surfactant concentration as well as in the peroxodisulfate ions concentration on __k__
Micellar Effects on the Reaction S2O82−+ Fe(CN)4(bpy)2−
✍ Scribed by Amalia Rodrı́guez; Marı́a del Mar Graciani; Marı́a Luisa Moyá
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- English
- Weight
- 125 KB
- Volume
- 191
- Category
- Article
- ISSN
- 0021-9797
No coin nor oath required. For personal study only.
✦ Synopsis
The reaction Fe(CN)4 (bpy)2- + S2 O8 2- has been studied in aqueous solutions of hexadecyltrimethylammonium chloride (CTAC) and bromide (CTAB), sodium dodecyl sulfate (SDS), dodecyl tricosaoxyethylene glycol ether (Brij35 ), and octylphenol(ethyleneoxide)9.5 ether (Triton X-100). The influence of changes in surfactant concentration on the reaction rate has been investigated. Experimental kinetic data show that the reaction rate is not affected by the presence of SDS, Brij35 , and Triton X-100 in the reaction medium within the surfactant concentration range studied. In CTAC and CTAB solutions the observed first order rate constant is much higher than that obtained in pure water, which can be explained by considering that the two anionic reactants are localized at the positively charged micellar surface. This is also in agreement with the observed decrease in the reaction rate when [cationic surfactant] increases. An increase in the surfactant concentration would provoke a decrease in the local concentration of the reagent in excess, S2 O8 2- ions, at the micellar surface, that is, at the reaction site, which would result in a decrease of the observed pseudo-first-order rate constant. Temperature was maintained at 298.2 K.
📜 SIMILAR VOLUMES
The reaction (4-CNpy ϭ 4-cyanopyridine) was studied 3Ϫ 2Ϫ Fe(CN) (4-CNpy) ϩ S O 5 2 8 in aqueous salt solutions in the presence of several electrolytes as well as in anionic, cationic, and nonionic surfactant solutions. In aqueous salt solutions the noncoulombic interactions seem to be important in
## Abstract Salt effects on the oxidation of the iron(II) complexes Fe(CN)~4~(bpy)^2−^, __cis__‐(CN)~2~(bpy)~2~ and Fe(bpy)~3~^2+^ by S~2~O~8~^2−^ as well as on the reaction Fe^2+^ + Co(NH~3~)~5~Cl^2+^ have been studied in concentrated electrolyte solutions at 298.2 K. We have gone from anion–anion
The ligand substitution reaction Fe(CN) 5 H 2 O 3Ϫ ϩ pyrazine : Fe(CN) 5 pyrazine 3Ϫ ϩ H 2 O has been studied in sodium dodecyl sulfate, SDS, hexadecyltrimethylammonium bromide, CTAB, and salt aqueous solutions at 298.2 K. Kinetics were studied in dilute and concentrated salt solutions and in SDS an
A study of the kinetic salt effects on the oxidation of Ru(NH 3 ) 5 pz 2ϩ (Pirazinepentaammineruthenium (II)) with (Peroxodisulphate) was carried out. The components of 2Ϫ S O 2 8 the experimental rate constant, k obs , were separated, and the true (unimolecular) electron transfer rate constant, k
## Abstract The kinetics of replacement of H~2~O by [Ru(NH~3~)pz]^2+^ (pz = pyrazine) in [Fe(CN)~5~H~2~O]^3−^ have been studied in various concentrated electrolyte solutions and in various water–cosolvent mixtures, at 298 K. Salt and cosolvent effects can be rationalized taking into account specifi