Study on electrochemical oxidation of 4-Chlorophenol on a vitreous carbon electrode using cyclic voltammetry

2013 ◽  
Vol 94 ◽  
pp. 192-197 ◽  
Author(s):  
Xiaoyue Duan ◽  
Lifeng Tian ◽  
Wei Liu ◽  
Limin Chang
2020 ◽  
Vol 16 (4) ◽  
pp. 421-427 ◽  
Author(s):  
Kemal V. Özdokur ◽  
Ceren Kuşcu ◽  
Fatma N. Ertaş

Background: Nowadays, polymeric composites modified with carbonaceous nanomaterials have been popular due to their greater application potentials in many application fields. However, the structural consistency of the composite prepared by electropolymerization suffers from agglomeration of Carbon Nanotubes (CNTs) probably due to their poor dispersion in the coating solution. Present study describes a new synthesis route for the preparation of polypyrrole/CNT composite film on a Glassy Carbon Electrode (GCE) via combining the ultrasonication and electrochemical pulsed deposition for the first time. The performance of the composite film was tested by monitoring the electrochemical oxidation of droxidopa which is used as a new psychoactive drug and synthetic amino acid precursor which acts as a prodrug to the neurotransmitters. Methods: The polypyrrole/CNT composite film was deposited onto a glassy carbon electrode via combining the ultrasonication and electrochemical pulsed deposition. The composite film was characterized by Scanning Electron Microscopy (SEM), Fourier Transfer Infrared Spectroscopy (FTIR), Electrochemical Impedance Spectroscopy (EIS) and Cyclic Voltammetry (CV). Then after, the electrochemical behavior of droxidopa was investigated on the GCE/PPy-CNT electrode. Results: SEM images of the surface morphology have revealed a more ordered film formation and enhanced conductivity of the surface has been confirmed by EIS measurements. The synergetic effect of this composite film was tested by monitoring the electrochemical oxidation of a new psychoactive drug; droxidopa at 0.45 V. The influence of solution parameters such as medium pH, pyrrole concentration and amount of CNT along with the instrumental parameters including applied pulse number on the peak formation was investigated by aid of cyclic voltammetry. Under the optimal conditions, by monitoring the oxidation peak in dp mode, two linear ranges have been observed in 4 - 20 μM which is well suited for droxidopa analysis in pharmaceutical preparations. The limit of detection (S/N=3) was calculated as 1.3 μM. Conclusion: Present study offers a fast, easy and sensitive method for the determination of droxidopa by providing a novel route for the preparation of PPy-CNT composite films for any further studies.


RSC Advances ◽  
2019 ◽  
Vol 9 (23) ◽  
pp. 13145-13152 ◽  
Author(s):  
Arafat Toghan ◽  
Ahmed M. Abo-Bakr ◽  
Hesham M. Rageh ◽  
Mohamed Abd-Elsabour

In this paper, we present promising results in the green electrochemical oxidation of catechol in the presence of three different thiol nucleophiles at the surface of a glassy carbon electrode in an aqueous solution using cyclic voltammetry (CV).


1995 ◽  
Vol 73 (3) ◽  
pp. 362-374 ◽  
Author(s):  
Benoit Daoust ◽  
Jean Lessard

The electrochemical behavior of N,N-dimethyl-N′-phenylformamidine hydrochloride was studied on a platinum electrode. The oxidation peak at +0.90 V vs. Ag/Ag+ 0.01 M (in CH3CN −0.1 M LiClO4) was assigned to the oxidation of the chloride anion. N,N-Dimethyl-N′-(4-chlorophenyl)formamidine and N,N-dimethyl-N′-(2-chlorophenyl)formamidine were isolated from the preparative electrolysis of this amidine hydrochloride. The electrochemical behavior of N-phenylbenzamidine hydrochloride and N-phenylcyclohex-3-enecarboxamidine hydrochloride was also studied at platinum and at vitreous carbon. Cyclic voltammetry of a number of amidines was performed. Only N-arylbenzamidines showed a reduction peak at potentials less negative than −3.0 V vs. Ag/Ag+ 0.01 M (discharge potential of the medium at vitreous carbon). Preparative electrooxidations of all amidines studied were unsuccessful because of strong and rapid passivation of the anode. Keywords: amidine, electrochemical oxidation, chloride, amidine hydrochloride.


2020 ◽  
Vol 16 (4) ◽  
pp. 393-403 ◽  
Author(s):  
Renjini Sadhana ◽  
Pinky Abraham ◽  
Anithakumary Vidyadharan

Introduction: In this study, solar exfoliated graphite oxide modified glassy carbon electrode was used for the anodic oxidation of epinephrine in a phosphate buffer medium at pH7. The modified electrode showed fast response and sensitivity towards Epinephrine Molecule (EP). The electrode was characterized electrochemically through Cyclic Voltammetry (CV) and Differential Pulse Voltammetry (DPV). Area of the electrode enhanced three times during modification and studies reveal that the oxidation process of EP occurs by an adsorption controlled process involving two electrons. The results showed a detection limit of 0.50 ± 0.01μM with a linear range up to 100 μM. The rate constant calculated for the electron transfer reaction is 1.35 s-1. The electrode was effective for simultaneous detection of EP in the presence of Ascorbic Acid (AA) and Uric Acid (UA) with well-resolved signals. The sensitivity, selectivity and stability of the sensor were also confirmed. Methods: Glassy carbon electrode modified by reduced graphene oxide was used for the detection and quantification of epinephrine using cyclic voltammetry and differential pulse voltammetry. Results: The results showed an enhancement in the electrocatalytic oxidation of epinephrine due to the increase in the effective surface area of the modified electrode. The anodic transfer coefficient, detection limit and electron transfer rate constant of the reaction were also calculated. Conclusion: The paper reports the determination of epinephrine using reduced graphene oxide modified glassy carbon electrode through CV and DPV. The sensor exhibited excellent reproducibility and repeatability for the detection of epinephrine and also its simultaneous detection of ascorbic acid and uric acid, which coexist in the biological system.


1989 ◽  
Vol 54 (1) ◽  
pp. 64-69 ◽  
Author(s):  
Roland Meier ◽  
Gerhard Werner ◽  
Matthias Otto

Electrochemical oxidation of [V(IV)O(nta)(H2O)]- (H3nta nitrilotriacetic acid) was studied in aqueous solution by means of cyclic voltammetry, differential pulse polarography, and current sampled DC polarography on mercury as electrode material. In the pH-range under study (5.5-9.0) the corresponding V(V) complex is produced by one-electron oxidation of the parent V(IV) species. The oxidation product is stable within the time scale of cyclic voltammetry. The evaluation of the pH-dependence of the half-wave potentials leads to a pKa value for [V(IV)O(nta)(H2O)]- which is in a good agreement with previous determinations. The measured value for E1/2 is very close to the formal potential E0 calculated via the Nernst equation on the basis of known literature values for log Kox and log Kred, the complex stability constants for the oxidized and reduced form, respectively.


2010 ◽  
Vol 132 ◽  
pp. 271-278 ◽  
Author(s):  
Dan Mei Yu ◽  
Chang Guo Chen ◽  
Shu Lei ◽  
Xiao Yuan Zhou ◽  
Guo Zhong Cao

The electrochemical oxidation of sodium borohydride (NaBH4) on Pt electrode in alkaline electrolyte with the addition of thiourea has been studied by means of cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and chronopotentiometry (CP). NaBH4 is readily to react with hydroxyl groups to release hydrogen through either direct oxidation or catalytic hydrolysis. The experimental results demonstrated that the addition of an appropriate amount of thiourea to the alkaline electrolyte resulted in the suppression of catalytic hydrolysis and diffusion of borohydride ions through the separation membrane.


1999 ◽  
Vol 44 (15) ◽  
pp. 2633-2643 ◽  
Author(s):  
G. Carreño ◽  
E. Sosa ◽  
I. González ◽  
C. Ponce-de-León ◽  
N. Batina ◽  
...  

1989 ◽  
Vol 34 (7) ◽  
pp. 899-904 ◽  
Author(s):  
V. Kadysh ◽  
J. Stradins ◽  
H. Khanina ◽  
G. Duburs

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