Th(IV)-hexacyanoferrate modified carbon paste electrode as a new electrocatalytic probe for simultaneous determination of ascorbic acid and dopamine from acidic media

ARTICLE

Th(IV)-hexacyanoferrate modified carbon paste electrode as a new electrocatalytic probe for simultaneous determination of ascorbic acid and dopamine from acidic media

Khalil Farhadi^I,*; Farshad Kheiri^I; Mirmaqsoud Golzan^II

^IDepartment of Chemistry, Faculty of Science, Urmia University, Urmia, Iran

^IIDepartment of Physics, Faculty of Science, Urmia University, Urmia, Iran

ABSTRACT

A stable carbon paste electrode (CPE) was prepared with Th(IV)-hexacyanoferrate (Th-HCF) ion pair and its electrochemical behavior was investigated by cyclic voltammetry. The apparent heterogeneous rate constant, k_s, and transfer coefficient, a, for electron transfer between Th-HCF ion-pair and CPE were calculated as 3.1 ± 0.1 s^-1 and 0.47, respectively. The surface coverage (Γ) of the proposed electrode was calculated as 7.06 × 10^-10 mol cm^-2. The proposed Th-HCF modified carbon paste electrode (THMCPE) showed a good electrocatalytic behavior with a significant shift toward negative potentials in oxidation of ascorbic acid (AA) and dopamine (DA) in acidic media (phosphate buffer solution, pH 3). The THMCPE exhibited excellent characteristics for simultaneous determination of AA and DA. Amperometric curves using the catalytic currents are linear for DA and AA concentrations in the ranges 8 × 10^-6 – 2 × 10^-3 and 1 × 10^-5 – 2 × 10^-3 mol L^-1 with detection limits 5.6 × 10^-6 mol L^-1 and 4.7 × 10^-6 mol L^-1, respectively. Diffusion coefficients of AA and DA in electrocatalaytic oxidation were calculated from chronoamperometric data.

Keywords: modified carbon paste, Th(IV)-hexacyanoferrate, ascorbic acid, dopamine

RESUMO

A estabilidade do eletrodo de pasta de carbono (CPE) foi obtida com o par eletrônico do Th(IV)-hexaferrocianeto (Th-HCF) e seu comportamento eletroquímico foi investigada por voltametria cíclica. A constante aparente do meio heterogêneo (ks) e o coeficiente de transferência(a), do par eletrônico Th-HCF e CPE, foram calculados como 0,47 e 3,1 ± 0,1 s^-1, respectivamente. A cobertura da superfície (Γ) do presente eletrodo foi calculada como 7,06 × 10^-10 mol cm^-2. O Th-HCF modificado com o eletrodo de pasta de carbono (THMCPE) apresentou um bom comportamento eletrocatalítico, com uma mudança significativa nos valores negativos do potenciais de oxidação do ácido ascórbico (AA) e da dopamina (DA), em meio ácido (solução tampão fosfato, pH 3). O THMCPE mostrou também excelentes características para a determinação simultânea de AA e DA. As curvas amperométricas utilizando o presente catalisador são lineares para a DA e AA , na faixa de concentrações entre 8 × 10^-6 – 2 × 10^-3 e 1 × 10^-5 – 2 × 10^-3 mol L^-1, com limites de detecção de 5,6 × 10^-6 mol L^-1 e 4,7 × 10^-6 mol L^-1, respectivamente. Os coeficientes de difusão para o AA e DA, na oxidação electrocatalítica, foram calculados a partir dos dados de cronoamperometria.

Introduction

Modified carbon electrodes have been widely used as sensitive and selective sensors in various electroanalytical methods. Among the various mediators used for electrode modification, solid metal hexacyanoferrates (MHCFs) were used as suitable modifier due to excellent electron transfer properties. Therefore, various transition metal cations have been used with hexacyanoferrate to fabricate MHCF modified electrodes, where M represents iron(III),^1,2 cadmium,³ chromium,⁴ cobalt,^5-8 copper,^9-12 gallium,¹³ indium,^14,15 lanthanum,^16, manganese,¹⁷ molybdenium,¹⁸ nickel,^19-21 palladium,²² platinum,²³ samarium(III),²⁴ silver,²⁵ titanium dioxide,²⁶ vanadium,²⁷ zinc,^28,29 , zirconium,³⁰ ruthenium oxide,³¹ terbium,³² cerium hexacyanoferrate,³³ neodymium,³⁴ gadolinium³⁵ or yttrium.³⁶ Most of these modified electrodes have been used to reduce the overvoltage, overcome the slow kinetics of many electrode processes and determination of one species as an analytical application.

Dopamine (DA) is an important kind of neurotransmitter in mammalian central nervous systems. Extreme abnormalities of DA levels cause symptoms of several diseases such as Parkinsonism.³⁷ The concentration of neurotransmitters in biological samples varies from species to species, in a wide range of from 10^-6 to 10^-3 mol L^-1. ^38,39 Ascorbic acid (AA) has been used for the prevention and treatment of common cold, mental illness, infertility, cancer and AIDS. ⁴⁰ In mammalian brain, AA is present along with several neurotransmitter amines including dopamine. Thus simultaneous determination of DA and AA is a problem of critical importance in the field of neurochemistry and biomedical chemistry. The increasing demand to determine these compounds led to the development of new techniques, among which electrochemical sensors attracted wide attention due to their advantages of simple, inexpensive and fast analysis in combination with high sensitivity and selectivity.^41,42 Both DA and AA are oxidisable compounds, characteristics which makes their detection possible by electrochemical methods based on anodic oxidation. However, a major problem is that both AA and DA are oxidized at nearly same potential with poor sensitivity at (unmodified) electrodes, which resulted in overlapped voltammetric responses making their discrimination highly difficult.⁴³ Electrochemical techniques with modified electrodes have received great interest for neurotransmitters determination in the presence of ascorbic acid as they are more selective and less time consuming and more versatile than those based on other colorimetric or spectrophotometric methods. Therefore, several attempts have been made to construct modified electrodes for the simultaneous determination of DA and AA such as self-assembled monolayer modified electrode,^44-46 self-assembled bilayer membrane modified glassy carbon electrode,⁴⁷ cationic self-assembled monolayer,⁴⁸ enzyme-based techniques,^49,50 organic electron mediators,^51,52 sol–gel composite electrode, ⁵³ multi-wall carbon nanotube, ^54,55 lipoic acid-coated carbon fiber microelectrodes,⁵⁶ poly(neutral red) modified electrodes, ^57-59 cationic and anionic surfactant modified electrode,^60,61 carbon paste electrode modified with iron (II) phthalocyanine complexes⁶² and tetrabromo-p-benzoquinone modified carbon past electrode.⁵⁷ However, still there is an expanding demand for the development of simple, sensitive, stable, reliable and selective sensors for effective sensing for DA and AA simultaneously. Among the carbon electrodes, the carbon paste electrode (CPE) is of particular importance. Simple and fast preparation, obtaining a new reproducible surface, the low residual current, porous surface and low cost of carbon paste are some advantages of CPEs over all other electrodes. Therefore, the CPE can provide a suitable electrode substrate for preparation of modified electrodes.

In the present work, we prepared a Th-HCF carbon paste electrode and examined its electrochemical behavior using different voltammetric techniques. To the best of our knowledge, there is no report about the preparation of modified electrodes using Th-HCF adduct. We also, studied the catalytic activity on molecules of biological interest, such as DA and AA.

Experimental

Chemicals

Th(NO₃)₄.5H₂O, K₄Fe(CN)_6, graphite fine powder and liquid paraffin were obtained from Merck and ascorbic acid (AA), dopamine (DA), were obtained from Fluka and used as received. All other chemicals used were of analytical grade. All solutions were prepared with twice distilled water. The buffer solution (0.1 mol L^-1) was made up from H₃PO₄ + KH₂PO₄, and the pH was adjusted with 0.1 mol L^-1 H₃PO₄ and/or 2.0 mol L^-1 KOH. AA and DA solutions were prepared just prior to use and all experiments were carried out at the ambient temperature of the laboratory (25 ºC). All solutions tested were deaerated by passing highly pure nitrogen (99.999%) before the electrochemical experiments and a continuous flow of nitrogen was maintained over the sample solution during the experiments.

Apparatus

Cyclic voltammograms were recorded by using Autolab PGSTAT30 Potentiostat/Galvanostat equipped with a frequency response analyzer (FRA4.9) and controlled by general purpose electrochemical system (GPES 4.9) software (Eco Chemie, Utrecht, The Netherlands). The cell used was equipped with a modified carbon paste disk as the working electrode, a glassy carbon electrode as an auxiliary electrode and with an Ag/AgCl as a reference electrode. All potentials in the text are quoted versus this reference electrode. A personal computer was used for data storage and processing. The pH was measured with a Zag Chemie model PTR79 pH/mV-meter (Tehran, Iran).

Preparation of Th-HCF modified CPE (THMCPE)

To a 20 mL acidic aliquot of a 0.1 mol L^-1 aqueous thorium solution was slowly added a 20 mL potassium hexacyanoferrate solution (0.1 mol L^-1) with continuous stirring until precipitation was completed. The resulting ion-pair precipitate was isolated by filtration, washed thoroughly with deionized water and dried at 40 °C. The composition of the formed ion pair was confirmed as Th[Fe(CN)₆] by the chemical analysis. The carbon paste electrode was prepared by hand-mixing of graphite powder, paraffin and Th-HCF ion-pair. The ratio of graphite powder to paraffin and to Th-HCF ion-pair was 70:15:15. The body of the carbon paste-working electrode was a Teflon rod with a hole (3 mm diameter and 5 mm deep) bored at one end for paste filling. Contact was made with a copper wire through the centre of the rod. The modified carbon paste was packed into the hole of the electrode body and levelled off with a spatula. The bare CPE was fabricated by the conventional procedure without Th-HCF ion-pair. The ratio of graphite to paraffin was 70:30.

Results and Discussion

Electrochemical behavior of THMCPE

The electrochemical behavior of THMCPE was studied using cyclic voltammetry. Cyclic voltammograms of THMCPE in 0.l mol L^-1 phosphate buffer solution (pH 3) at different low scan rates are shown in Figure 1-A. As seen, the voltammograms consisted of a pair of well-defined redox peaks with peak-to-peak potential separation (ΔE_p = E_pa - E_pc) about 67 mV at potential scan rates lower than 60 mVs^-1. Also, the formal potential (Eº = (E_pc+ E_pa)/2) is almost independent of the potential sweep rates below 60 mVs^-1, suggesting facile charge transfer kinetics over this range of sweep rates. On the other hand, peak currents of the voltammograms are linearly proportional to the scan rate indicating a surface-immobilized redox couple. At potential scan rates higher than 100 mV s^-1, the peak separation increases, indicating the limitation arising from charge transfer kinetics (Figure 1-B). Also, the ratio of cathodic to anodic peak currents was almost constant and peak currents are directly proportional to the square root of potential scan rates, as predicted for a diffusion controlled electrode process system (Figure 1-C).

The effect of pH on the electrochemical behavior of the THMCPE was investigated by cyclic voltammetry in 0.1 mol L^-1 phosphate buffer solution of various pH values (2-10) containing 0.1 mol L^-1 KCl as supporting electrolyte. The obtained results showed a slightly decrease of the current response with increasing pH value due to a lower stability of the hexacyanoferrate-Th(IV) association. The mediator coating is stable at pH lower than 6.

The stability of THMCPE as the rate of loss of electrochemical activity was examined by repetitive scans in a in 0.l mol L^-1 phosphate buffer solution (pH 3). This rate was evaluated as decrease in anodic or cathodic charge in consecutive potential scan cycles. The obtained results showed that the anodic and cathodic peak currents of THMCPE decrease 5% after 100 cycles at potential scan rates 20-50 mV s^-1 without any considerable change in potential peak separation. Furthermore, no significance change in activity of THMCPE was observed after almost 40 times use within two months.

An approximate estimation of the surface coverage of the electrode was made by adopting the method used by Laviron.⁶³ According to this method, total amount of charge (Q) is related to the surface concentration of electroactive species, Γ^*, by the following equation:

Where n represents the number of electrons involved in reaction, A is the surface area of the electrode, Γ^* (mol cm^-2) is the surface coverage and Q is total amount of charge which can be obtained from the integration of cyclic voltammetry peak and F is Faraday constant. The average amount of electrode surface coverage for anodic peaks recorded at 60 mV s^-1 (as a low scan rate) with surface area 0.125 cm² was 7.06 × 10^-10 mol cm^-2. At higher potential scan rates, the peak separation increases and the apparent coverage is slightly diminished probably due to drop in charge transfer through a modified layer, which becomes rate-limiting at higher scan rates.

The transfer coefficient, α, and the heterogeneous rate constant, k_s, of a surface-confined redox couple can be evaluated from cyclic voltammetric experiments and using the variation of anodic and cathodic peak potentials with scan rate, according to the procedure of Laviron.⁵⁷ The obtained results showed that the E_p values are linearly proportional to log ν, for scan rates higher than 100 mV s^-1 (ΔE_p> 200/n mV see Figure 1, inset B). Under these conditions, the following equations could be used to determine the electron transfer rate constant between hexacyanoferrate Th-HCF and CPE :

where:

According to equations 2 and 3, the plot of E_p - E_o= f (log ν) yields two straight lines with a slope equal to 2.3 RT/anF for the cathodic peak and 2.3 RT/ (1 - α)nF for anodic peak. Using these slopes and also equation 4, the values of α and k_s were found to be 0.47 and 3.1 ± 0.1 s^-1.

Electrocatalytic oxidation of AA

Figure 2 shows the CVs obtained from the oxidation of AA at bare CPE and THMCPE. The curves (A) and (B) are corresponding to 0.1 mol L^-1 buffer phosphate solution (pH 3) in the absence and presence of 3b × 10^-4 mol L^-1 AA, respectively, at the bare CPE. The curve (C) corresponds to THMCPE and curve (D) corresponds to oxidation of 3 × 10^-4 mol L^-1 AA at the THMCPE. As can be seen, at the bare electrode, the CV exhibited a broad peak at potential of 590 mV with poor current response for AA oxidation. In contrast, at the THMCPE, the oxidation current increased greatly at a reduced peak potential of 260 mV and the corresponding cathodic peak disappeared on the reverse scan of potential. The anodic peak current increased with the increase in the concentration of AA. The significant negative shift in the peak potential about 330 mV and the enhanced current response observed with the THMCPE compared to bare CPE indicate a strong electrocatalytic effect of Fe(CN)₆^3-/Fe(CN)₆^4- redox couple in the THMCPE towards the oxidation of AA.

Electrocatalytic oxidation of DA

Electrocatalytic activity of the bare electrode and the THMCPE, were obtained in 0.1 mol L^-1 phosphate buffer (pH 3) in presence and absence of 3 × 10^-4 mol L^-1 DA were presented in Figure 3. Cyclic voltammogramms (A) and (B) show the behavior of bare electrode in the presence and absence of 3×10^-4 mol L^-1 DA and cyclic voltammograms (C) and (D) were obtained for same solutions using THMCPE, respectively. From the obtained CVs, it can be observed that at the THMCPE, the oxidation current increased greatly with a decrease in oxidation potential about 200 mV in comparison to bare CPE. These observations showed an efficient electrocatalytic activity for the oxidation of DA using proposed chemically modified carbon paste electrode.

Effect of pH on the oxidation of AA and DA

The influence of solution pH on the electrochemical response of the THMCPE towards the oxidation of AA and DA was studied in pH range from 2 to 9. Figures 4A and 4B show the variation of peak potential and peak current with respect to changes in the pH of the electrolyte, respectively. In both figures, the curve (a) corresponds to 3 × 10^-3 mol L^-1 AA and (b) corresponds to 1 × 10^-3 mol L^-1 DA. It was observed that the peak potential for both AA and DA shifted negatively with the increase in pH of the electrolyte. Also, the current responses for AA and DA oxidation were higher at acidic pH conditions. As can be seen from figures, while the difference between potential shifts for AA and DA oxidation were nearly constant at all tested pH (see Figure 4-A, curves a and b), the obtained current responses were diminished with the increase in pH of the electrolyte. On the other hand, the proposed modified electrode showed excellent stability as well as reproducible signals in acidic solutions. Therefore, a pH of 3 was chosen for oxidation studies of AA and DA with THMCPE.

Chronoamperometric studies of AA and DA oxidation

Double potential step chronoamperometry, as well as other electrochemical methods was employed for investigation of electrochemical process at the chemically modified electrodes. The current–time curves of THMCPE were obtained by setting the working electrode potential at 0.80 V (at the first potential step) and at 0.00 V (at second potential step) vs. Ag /AgCl for the various concentration of ascorbic acid and dopamine in buffered aqueous solutions (pH 3) and also for modified electrode in the absence of AA and DA. For an electroactive material with a diffusion coefficient (D), the current corresponding to the electrochemical reaction (under diffusion controlled) is described by Cottrell equation:⁶⁴

Where D is apparent the diffusion coefficient (cm² s^-1) and C₀ is the apparent bulk concentration (mol cm^-3), respectively. Diffusion coefficient is easily calculated from the slope of the plot of I vs. t ^-1/2. Chronoamperograms using modified electrode for solution containing AA and/or DA represented a typical I-t^-1/2 curves which indicates that the observed currents have a diffusion control nature. The mean value of the D for ascorbic acid and dopamine were found 4.06 × 10^-5 and 4.43 × 10^-5 (cm² s^-1), respectively.

Simultaneous determination of DA and AA

Figure 5 shows the CVs of a mixture of AA and DA at bare CPE and at THMCPE in 0.1 mol L^-1 phosphate buffer solution (pH 3). In this figure, the curves (a) and (b) correspond to the oxidation of a mixture of 6 × 10^-4 mol L^-1 AA and 3 × 10^-4 mol L^-1 DA at bare electrode and THMCPE, respectively. As can be seen, a poor current response was observed at the bare CPE in the presence of a mixture of DA and AA. In contrast, two well-defined anodic peaks at the potential of 260 and 470 mV were observed for the oxidation of AA and DA, respectively, at the THMCPE. The difference between the two peak potentials is about 190 mV and the current response increased with the increase in the concentration of AA and DA. Figure 6 shows the CVs of oxidation peak of various concentrations of AA in presence of 3 × 10^-4 mol L^-1 DA .The curves (a), (b) and (c) correspond to the presence of 1 × 10^-4, 3 × 10^-4 and 6 × 10^-4 mol L^-1 AA. As can be seen, while the current response at the DA oxidation peak is fix, the current response at the AA peak increased with the increase in the concentration of AA. Similarly, Figure 7 shows the CVs recorded for the solutions containing various concentrations of DA in the presence of 3 × 10^-4 mol L^-1 AA. As can be seen from the curves (a), (b) and (c) correspond to the oxidation of 5 × 10^-5, 1 × 10^-4 and 3 × 10^-4 mol L^-1 DA, the current response at the DA oxidation peak increased with the increase in the concentration of DA without any change in the AA peak. It should be noted that in contrast with the majority of the electrochemical studies reported in literature for the simultaneous determination of AA and DA, no shift in the potential peaks of AA or DA was observed in all mixed solutions using the proposed modified electrode. These results indicated that the THMCPE have an excellent catalytic activity for simultaneous determination of AA and DA at reduced and well-separated peak potentials with enhanced sensitivity. This ability to measure AA and DA in a mixture has significant attraction in biological and chemical research.

Amperometric determination of AA and DA

Typical amperometric signals were obtained by successive addition of AA to continuously stirred phosphate buffer solution (pH 3). Figure 8-A shows a typical amperometric response obtained at a fixed potential of 300 mV for successive addition of 250 µ mol L^-1 AA. The response time was about 5 s and the obtained currents using THMCPE were 5-6 times larger than that on bare electrode at the same condition. Figure 8-B shows the calibration graph for determination of a linear response to AA in the concentration range from 1 × 10^-5 to 2 × 10^-3 mol L^-1 with a correlation coefficient of 0.9953. When the ratio of signal to noise is 3 the detection limit (LOD) for AA was 5.6 µmol L^-1. Similarly, Figure 9-A depicts the amperometric response for DA. The applied voltage was at 500 mV for successive addition of 180 µmol L^-1 DA. The THMCPE exhibited rapid response to the changes in the concentration of DA (less than 6 s). Figure 9-B presents linear response to DA in the concentration range from 8 × 10^-6 to 2 × 10^-3 mol L^-1. Correlation coefficient was obtained 0.9904 with LOD 4.7 µmol L^-1 when S/N was 3. The proposed electrode showed a good repeatable and reproducible response for DA and AA. The peak current values for DA and AA were detected with a relative standard deviations of 3.2% and 3.5%, respectively. It must be noted that we evaluated the electrocatalytic oxidation of some oxidisable inorganic ions such as thiosulfate, nitrite as well as some inorganic and organic molecules such as hydrazine and uric acid using proposed probe. In all cases no significant electrocatalytic effect were observed.

Conclusions

The electrochemical properties of THMCPE were studied as new chemically modified carbon paste electrode. The THMCPE showed an excellent electrocatalytic activity towards AA and DA and applied for the simultaneous determination of ascorbic acid and dopamine in phosphate buffer (pH 3) with good sensitivity and selectivity. The oxidation of AA at the THMCPE occurred at the potential of 270 mV with a great increase in the peak current compared to that of the bare carbon paste electrode. Electrocatalytic oxidation of DA was observed at the potential of 470 mV with a great increase in response peak current toward bare CPE. The voltammetric signals of AA and DA were obtained in two well-defined peaks with a peak separation of 200 mV. A favourable electrocatalytic reaction between the THMCPE and AA and DA shifted their oxidation potential to a less positive potential. Although, the detection limit of proposed method for DA and AA is slightly higher than the some reported works in the literature, but the electrocatalytic ability toward AA and DA in acidic media (pH 3) with wider linear range, good reproducibility and stability are the most important aspect of the proposed modified electrode in comparison to other reports.

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Received: August 26, 2007

Web Release Date: August 28, 2008

Publication Dates

• Publication in this collection
  03 Oct 2008
• Date of issue
  2008

History

• Accepted
  28 Aug 2008
• Received
  26 Aug 2007