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This paper describes a rapid and reliable method for dopamine (DA), ascorbic acid (AA), and uric acid (UA) determination in human urine using a cathodically pretreated poly(1-aminoanthraquinone) (PAAQ)-modified electrode. By applying a simple cathodic pretreatment to the PAAQ electrode well-defined voltammetric peaks for AA, DA, and UA were obtained. The pretreated PAAQ showed good selectivity, sensitivity, and repeatability for measuring AA, DA, and UA with detection limits of 2.50 × 10, 3.05 × 10, and 1.15 × 10 M, respectively. The practical applicability of the modified electrode is illustrated by selective measurements of AA and UA in human urine without any preliminary treatment. Recovery values between 94.8 and 102 % for AA and between 77.8 and 100 % for UA were obtained with a relative standard deviation of 2.74 and 2.98 %, respectively. [ABSTRACT FROM AUTHOR]

A simple Co3O4 modified carbon paste electrode (CPE) was developed as an electrochemical sensor for the selective detection and quantification of dopamine (DA) via fastest synthesis and fabrication methods. The solution combustion method and bulk modification techniques were sequentially used for the preparation of the sensor. The modifier was characterized using different techniques such as PXRD, FT-IR, SEM and TG-DSC. The fabricated sensor shows a wide linear dynamic range of 80 µM-300 nM, low detection limit, excellent reproducibility and high stability. The differential pulse voltammetry (DPV) and cyclic voltammetry (CV) techniques were extensively used for the electrochemical studies. The same electrode was used for detecting DA in the solution of coexisting ascorbic acid (AA) and uric acid (UA). Well resolved peaks and good current sensitivity of this electrochemical sensor extended its utility in determining DA in blood serum at physiological pH. [ABSTRACT FROM AUTHOR]

A selective determination of levodopa (LD) in the presence of ascorbic acid (AA) and uric acid (UA) has been investigated at a glassy carbon electrode modified with reduced graphene oxide (rGO). The graphene oxide was synthesized chemically by Hummers method and characterized by energy-filtered transmission electron microscopy (EF-TEM). The reduced graphene oxide modified glassy carbon electrode (rGO/GCE) showed excellent electrochemical performance in the simultaneous electrochemical detection of LD, AA, and UA due to the unique properties of graphene, such as large surface area, facile electronic transport and high electrocatalytic activity. The redox characteristics of rGO/GCE were investigated with cyclic voltammetry (CV) and differential pulse voltammetry (DPV). Well-resolved oxidation peak potentials, corresponding to the oxidation of AA, LD, and UA, were observed from their mixture solution at 0.098, 0.285, and 0.423 V, respectively. The rGO/GCE showed that LD can be detected without the interference of AA and UA. Under the optimized conditions, the oxidation peak current of LD is linear with the concentration of LD from 2.0 to 100 μM with the detection limit of 1.13 μM (S/N = 3). The present electrode system was also successfully applied to direct determination of LD in commercially available tablets and urine samples. [ABSTRACT FROM AUTHOR]

In this study a Photoelectrochemical Cell (PEC) constructed with inexpensive materials photodegraded selected organic compounds present in model waste waters, with the concomitant production of electrical current. Organic substrates dissolved in salt water included formic acid, 2-propanol, 1,2-dihydroxybenzene and ascorbic acid. Significant degradation of ascorbic acid was achieved when the cell was illuminated with a household 60 W tungsten light bulb, although better results were achieved with UV sources. Degradation of all the compounds was found to occur by zero order kinetics, and the PEC was shown not to work appreciably in dark conditions. Using a conventional light bulb, a formic acid PEC produced a power density of 19.1 ± 2 mW m. When exposed to natural daylight, a power density of 31.5 ± 2 mW m was achieved. There is considerable scope for scale up of this device for exterior use. [ABSTRACT FROM AUTHOR]

The electrocatalytic behavior of uric acid has been investigated with a glassy carbon electrode modified with p-aminobenzene sulfonic acid through electrochemical polymerization. This resulting electrode shows an excellent electrocatalytic response to uric acid and ascorbic acid, with a peak-to-peak separation of 0.267 V in a 0.1 mol L−1 phosphate buffer solution (PBS) at pH 7.0. These results indicate that the proposed electrode can eliminate the serious interference of ascorbic acid, which coexists with uric acid in body fluids. Differential pulse voltammetry (DPV) was used for detecting uric acid with selectivity and sensitivity. The anodic peak current of uric acid was proportional to its concentration in the range of 1.2 × 10−7–8.0 × 10−4 mol L−1, with a detection limit of 4.0 × 10−8 mol L−1. The proposed method has been applied with satisfactory results to the determination of uric acid in human urine without any pretreatment. [ABSTRACT FROM AUTHOR]

Cyclic voltammetry and chronoamperometry were used to investigate the electrochemical behavior of ascorbic acid at a carbon paste electrode modified with 2,2′-(1,8-octanediylbisnitriloethylidine)-bis-hydroquinone (1,8-OBNEBHQ). The modified carbon paste electrode showed high electrocatalytic activity toward ascorbic acid; the current was enhanced significantly relative to the situation prevailing when an unmodified carbon paste electrode was used. The electrocatalytic process was highly dependent on the pH of the supporting electrolyte. The apparent charge transfer rate constant, ks, and transfer coefficient, α, for electron transfer between 1,8-OBNEBHQ and carbon paste electrode were calculated as 20.2 ± 0.5 s−1 and 0.47, respectively. Using differential pulse voltammetry, the calibration curves for AA were obtained over the range of 5–30 and 40–1,500 μM, respectively. The detection limit (kσ, k = 2) was 0.6 μM. With good selectivity and sensitivity, the present method provides a simple method for selective detection of ascorbic acid in biological samples. [ABSTRACT FROM AUTHOR]

Binuclear copper complex (2-[bis(2-aminoethyl)amino]ethanol, 4,4′-bipyridine bridged dicopper(II) complex) was grafted onto the surface of a glassy carbon electrode (GCE) using the cyclic voltammetric method in a phosphate buffer solution (PBS). The modified electrode resulted in efficient electrocatalytic activity for anodic oxidation of uric acid (UA) and ascorbic acid (AA) via a substantial decrease in anodic over-potentials for both compounds. Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) using this modified electrode result in two well-resolved anodic waves for the oxidation of UA and AA in mixed solution, making possible the simultaneous determination of both compounds. Linear analytical curves were obtained in the ranges 5.0–300.0 μM and 5.0–160.0 μM for UA and AA concentrations through DPV methods, respectively. The detection limits were 2.0 μM of UA and AA. This electrode was used for UA and AA determinations in urine samples with satisfactory results. [ABSTRACT FROM AUTHOR]

The effect of ascorbic acid (AA) on the corrosion of mild steel in sulphuric acid solution has been investigated by open circuit potential (OCP) and polarization measurements. AA was observed to shift the OCP to more positive potentials with increasing concentration. The polarization curves revealed that AA inhibited the anodic metal dissolution reaction, although this effect became negligible at high anodic overpotentials. The trend of inhibition efficiency with concentration showed that efficiency increased rapidly at low concentrations, remained almost steady at intermediate concentrations and increased again at high concentrations. The mechanism of inhibition was considered in terms of initial chemisorption of AA according to the Temkin isotherm, followed by formation of chelate compounds with Fe2+ ions at high concentrations. EDS and AFM analyses of the electrode surface support the proposed inhibition mechanisms. [ABSTRACT FROM AUTHOR]