Abstracts

Article

N-propylpyridinium Chloride Silsesquioxane Polymer Film on Graphite: Electrochemical Study of a Hexacyanoferrate (II) Ion Immobilized Electrode for Oxidation of Ascorbic Acid

Rení V. S. Alfaya, Yoshitaka Gushikem* and Antonio A. S. Alfaya

Instituto de Química, Universidade Estadual de Campinas, CP 6154, 13083-970 Campinas-SP, Brazil

Introduction

N-propylpyridiniumchloride silsesquioxane (Figure 1) is a new water soluble polymer¹ whose most important characteristic is its capacity for forming a stable thin film on substrate surfaces such as aluminum oxide, celullose fibers, silica gel or glass surfaces^2,3. The polymer is a strong anionic exchanger and since the immobilized counterion is the pyridinium ion, the exchange reaction does not depend on the solution pH⁴. The strength with which an anionic species is adsorbed and retained on the polymer surface depends essentially on its affinity coefficient for the solid phase i.e. the ratio between the adsorbate concentration on the solid phase and in solution phase⁵.

Considering the excellent capacity of this new anionic exchanger polymer for forming a thin film on the graphite surface, ferrocyanide ion was adsorbed on the resulting modifed surface by an ion exchange reaction, since it is known that propylpyridinium chloride groupsare good ion exchangers and have high affinity for this ion⁶.

The electrochemical properties of this ion were investigated and applied in the electrocatalytic oxidation of ascorbic acid. Due to its importance in biochemical and biomedical processes, development of new methods of analyses by means of electrochemical sensors based on carbon paste modified electrodes^6-11, carbon fiber¹², glassy carbon^13,14, tick-film carbon¹⁵ and polymer-coated electrodes^16-22 have been tested.

To probe the potential usefulness of the modified electrode as a chemical sensor, the studies were extended to analyze ascorbic acid in commercially available vitamin C tablets and in processed orange juices.

Experimental

The polymer 3-n-propylpyridiniumchloride silsesquioxane, referred to as SiPy⁺Cl, was prepared according to the method described elsewhere¹. Analytical grade potassium ferrocyanide and ascorbic acid were used as received without any previous purification.

Polymer coated graphite

An electrode was made by inserting, under pressure, a spectroscopically pure 8 mm diameter graphite cylinder in the hole of a Teflon bar with same internal diameter. The end of the graphite surface was polished and the clean surface was immersed in an aqueous solution of the polymer SiPy⁺Cl^- (5 % w/v) for 30 min and then dried at room atmosphere. The electrode, referred to as graph/SiPy⁺Cl^-, was immersed in a solution of potassium ferrrocyanide (20% m/v) for 10 min and then rinsed with pure water and dried. The resulting modified electrode is designated as (graph/SiPy⁺)₄[Fe(CN)₆ ]^4-.

Electrochemical measurements

The electrochemical measurements were made by immersing the prepared electrode, as described above, in a cell with 0.1 mol dm^-3 KCl solution by using a platinum wire as the counter electrode and SCE as the reference electrode. Cyclic voltammetry measurements were made by sweeping the potential between -0.2 and 0.5 V at a scan rate of 20 mV s^-1.

In amperometric detection successive volumes of 0.01 mol dm^-3 ascorbic acid were added in an electrochemical cell filled with 20 cm³ of 0.1 mol dm^-3 KCl solution and at a fixed potential of 0.2 V, at pH 5.5. All the electrochemical measurements were carried out under pure argon atmosphere.

Ascorbic acid in real samples (vitamin C tablets) from three different suppliers were analyzed. The tablets (~4 g) were dissolved in bidistilled water and the volume completed to 500 cm³ (solution A). The amperometric curves were obtained by adding successive aliquots of 200 mdm³ of solution A into a cell filled with 20 cm³ of 0.1 mol dm^-3 KCl solution at pH 5.5. The observed current against time plot was compared with that obtained for standard ascorbic acid solution. In processed juices, vitamin C was determined by using similar procedure.

Vitamin C in tablets and in juices was also determined by the standard volumetric technique by using the reagent 2,6-dichlorophenolindophenol (dpip)^23-25.

Results and Discussion

The hexacyanoferrate (II) ion is bound to the electrode surface by an electrostatic interaction and gives a redox pair at a midpoint potential E_m= 0.14 V [E_m= E_pa + E_pc)/2, where E_pa and E_pc are the anodic and the cathodic peak potentials, respectively] in 0.1 mol dm^-3 KCl solution at pH 5.5 (Figure 2c). By integrating the area under the anodic or cathodic curves and considering that the geometric area of the electrode is 0.5 cm², the quantity of estimated ferrocyanide ion was ~ 2x10^-5 mmol cm^-2. For bare graphite and graph/SiPy⁺Cl^- electrodes no redox pair in the range of the potential swept was observed (Figures 2, a and b, respectively).

Figure 3 shows the influence of the solution pH on E_m. Between pH 4.5 and 6.5 the E_m remained nearly constant and increased at pH values lower than 4. An explanation for such behavior is presumably related to the tendency of the hexacyanoferrate (II) ion to form a stable ion pair with H⁺ with an association constant³⁰ log K_a= 4.28. Such increase of midpoint potential was already observed for an electrode of SiO₂/TiO₂/[Fe(CN)₆ ]⁴ where hexacyano-ferrate (II) is strongly adsorbed on the titanium oxide surface, ºTiOH₂⁺[Fe(CN₆ )₆]^4- by electrostatic interaction²⁶ (ºTiOH₂⁺ stands for protonated hydrous Ti(IV) oxide grafted to a silica gel surface).

In order to check the stabiltiy of the electrode under exhaustive operation conditions, the anodic and the cathodic peak current intensities were measured against the number of oxidation-reduction potential cycles (Figure 4). Upon cycling the potential between -0.2 and 0.5 V at a sweeping velocity of 20 mV s^-1, the anodic and cathodic peak current intensities did not show any significant decrease resulting from release of the electroactive species to the solution phase at the end of 60 redox cycles. Such degree of adherence on the surface is presumably related to a high affinity coefficient of the hexacyanoferrate (II) ion to the immobilized pyrydinium ion in the solid phase.

Oxidation of the ascorbic acid

Figure 5 shows the ascorbic acid oxidation on the (graph/SiPy⁺)₄[Fe(CN)₆ ]^4- electrode surface. The cyclic voltammetry curve in the presence of 1.0x10^-3 mol dm^-3ascorbic acid solution (pH 5.5) shows a considerable enhancement of the electrode anodic peak current at 0.19 V (curve c) in comparison with the current peak in absence of the acid (curve b). On the bare electrode graph/SiPy⁺Cl^- (curve a) no current is observed for 1.0x10^-3 mol dm^-3 ascorbic acid solution (pH 5.5). The acid oxidation reactions at the solid-solution interface can be described by the following reactions:

2(graph/SiPy⁺)₄/[Fe^II (CN)₆]^{4 -}®

2(graph/SiPy⁺)₄/[Fe^III (CN)₆]^3- + 2e^-

2(graph/SiPy⁺)₄/[Fe^III (CN)₆]^3- + H₂AA ®

2(graph/SiPy⁺)₄/[Fe^II (CN)₆]^{4 -} + 2AA + 2H ⁺

where H₂AA is the ascorbic acid and AA the dehydroascorbic acid.

Amperometric detection

Figure 6a shows the amperometric curve obtained upon addition of the ascorbic acid into an electrochemical cell at a fixed E_pa= 0.2 V. It is noteworthy that the response time is very fast and there is no indication that the product is being adsorbed on the electrode surface during the experiment. Such adsorption could interfere on the electrode response, by suppressing the signal. Figure 6b shows the plot of the current peak against ascorbic acid concentrations. A linear correlation for concentrations of the acid between 0.25x10^-4 and 2.5x10^-4 mol dm^-3 is observed with a detection limit of 0.25x10^-4 mol.dm^-3 and sensitivity of 0,25x10^-5 mol dm^-3. Therefore, the present electrode has a potential use as sensor for ascorbic acid.

Determination of ascorbic acid in real samples

The results of the analyses of vitamin C in tablets and juices (an average of five determinations) obtained using the electrode are presented in Table 1. The values found are compared with those obtained following the recommended ascorbic assay procedure by using the dpip reagent²³. The amperometric measurements results are found with 95% confidence level and by applying the paired t-test a minimum with 95% confidence.

Conclusions

The electrode (graph/SiPy⁺)₄/[Fe^II (CN)₆]^4- was stable under the operation conditions. The results obtained by using the present electrode are very good considering that other chemical species which could be present, especially in the processed juices, did not interfere in the results. The advantages of using the present electrode are the small time dedicated to the analytical procedure and the fact that it is easily prepared and regenerated. The electrode was relatively sensitive in detecting, using the chronoamperometry technique, a concentration limit of 0.25x10^-4 mol dm^-3 ascorbic acid.

Acknowledgments

Y. G. is indebted to FAPESP and PRONEX for financial support; R. V. S. A. and A. A. S. A. are indebted to CAPES/PICD and CNPq for a fellowship

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Received: July 12, 1999.

FAPESP helped in meeting the publication costs of this article.

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