Electrochemical Studies and the Electrode Reaction Mechanism of Ferrocene and Naphthoquinones in Microemulsion Medium at GC Electrode
International Journal of ELECTROCHEMICAL SCIENCE • 2020
معلومات البحث
المؤلفون
M, Abdallah 1,2*
, Ahmed Alhabi2
, Moataz Morad 2
, Ahmed M Hameed 2
, Salih S. Al-Juaid 3
,
N. Foad 1and E.M. Mabrouk1
الكلمات المفتاحية
Electrode reaction mechanism, CV, RDV and chronocoulometry techniques,
naphthoquinones, GC electrode.
المجلة العلمية
International Journal of ELECTROCHEMICAL SCIENCE
الناشر
Not Available
المجلد
15
العدد
Not Available
الصفحات
Not Available
publication.type
International
رابط البحث
Not Available
المواد المرفقة
Not Available
الملخص
The electrochemical behavior of 1,4-napthoquinone (1,4-NAQ) and 2-methyl-1,4-naphthoquinone (2-
Me-1,4-NAQ) was investigated in bis-(2-ethylhexyl) sulfosuccinate (EHSS) anionic surfactant and its
microemulsion system as well as in aqueous medium using cyclic voltammetry, rotating disk
voltammetry and chronocoulometry techniques. The voltammograms of both compounds in all media
exhibit a single redox couple and the ratios of Ipa/Ipc is slightly less than unity in all media. The Ip – v
1/2
plots gave linear correlations slightly deviated from the origin which denoting that the electrode reaction
is mainly controlled by diffusion with slight adsorption contribution. For 1,4-NAQ and 2-methyl-1,4-
NAQ in all media, the peak separation (∆ Ep), is not close to the theoretical value of completely reversible
2-electron transfer process (30 mV) which denotes that an ECE reaction nature and the reduction process
of both compounds is quasi-reversible. This behavior is further confirmed by the cathodic shift of the
rotating disk voltammograms as the angular velocity increases and the data of this technique were found
in a good agreement with that obtained from cyclic voltammetry. The diffusion coefficient values of
both compounds were calculated and the electrode reaction mechanism was suggested.
Me-1,4-NAQ) was investigated in bis-(2-ethylhexyl) sulfosuccinate (EHSS) anionic surfactant and its
microemulsion system as well as in aqueous medium using cyclic voltammetry, rotating disk
voltammetry and chronocoulometry techniques. The voltammograms of both compounds in all media
exhibit a single redox couple and the ratios of Ipa/Ipc is slightly less than unity in all media. The Ip – v
1/2
plots gave linear correlations slightly deviated from the origin which denoting that the electrode reaction
is mainly controlled by diffusion with slight adsorption contribution. For 1,4-NAQ and 2-methyl-1,4-
NAQ in all media, the peak separation (∆ Ep), is not close to the theoretical value of completely reversible
2-electron transfer process (30 mV) which denotes that an ECE reaction nature and the reduction process
of both compounds is quasi-reversible. This behavior is further confirmed by the cathodic shift of the
rotating disk voltammograms as the angular velocity increases and the data of this technique were found
in a good agreement with that obtained from cyclic voltammetry. The diffusion coefficient values of
both compounds were calculated and the electrode reaction mechanism was suggested.
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