Kinetic study of the reaction between Fe2+-oxalate and 2,6-dichlorophenolindophenol

 
This item is provided by the institution :
University of Ioannina
Repository :
Repository of UOI Olympias
see the original item page
in the repository's web site and access all digital files if the item*
share



1998 (EN)
Kinetic study of the reaction between Fe2+-oxalate and 2,6-dichlorophenolindophenol (EN)

Karayannis, M. I. (EN)

Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείας (EL)
Karayannis, M. I. (EN)

Ascorbic acid present in natural products is often analyzed by its reducing effect on 2,6-dichlorophenolindophenol (DCPI). In case of coexistence of Fe(II) in natural samples and if oxalic acid is used for their extraction and stabilization, a significant interference is observed. The reaction of Fe2+ with 2,6-dichlorophenolindophenol (DCPI) in acidic solutions in the presence or absence of oxalate ions was investigated. The reaction was studied with a Stopped-Flow Spectrophotometer (S.F.S) equiped with a data acquisition system, which allows the determination of initial rates and reaction rate constants. Results for the effect of the concentrations of all the reagents of the reaction are presented. During the experimental work all concentrations of the reagents were kept in such levels to make the reaction first-order in respect of DCPI. An interesting finding is, that, although Fe2+ and C2O42- ions do not react separately with DCPI (or react very slowly), they react very rapidly in mixtures and show a strong synergetic effect. The experimental data At with the mechanism of the formation of intermediates FeC2O4 and [Fe(C2O4)(2)](2-). The proposed rate law agrees with the above mechanism and the experimental results. The value k(c) = (1.6 +/- 0.2) X 10(5) M-1.s(-1) was calculated for the second-order rate constant of the reaction of FeC2O4 and DCPI. (C) 1998 John Wiley & Sons, Inc. (EN)

ascorbic-acid (EN)

Πανεπιστήμιο Ιωαννίνων (EL)
University of Ioannina (EN)

International Journal of Chemical Kinetics (EN)

English

1998

<Go to ISI>://000077151300009



*Institutions are responsible for keeping their URLs functional (digital file, item page in repository site)