Determination of L-Ascorbic Acid by Adsorption Potentiometry with Carbon Paste Electrode

Abstract

Abstract This paper reports the potentiometric measurement of ascorbic acid in the solution of 0.10 mol/L NaOH-0.1 mol/L NaCl using carbon paste (the mixture of spectroscopic graphite powder and di-iso-octyl phthalate) electrode(room temperature 15°C), with the linear range 7.0 × 10−7 × 4.0 × 10−5mol/L, average response slope 95mV/decade and detection limit 1 × 10−7mol/L. Phenol, sulfite, Mn2+ and so on pose no interference to the measurement of ascorbic acid. This method is characterized by fine selectivity, reproducibility and accuracy. The potential response behavior is caused chiefly by chemisorption of ascorbic acid to the surface of the carbon. Each year yields a number of papers concerning the determination of ascorbic acid by various methods, including gas chromatographymass spectrometry1, capillary electrophoresis2, spectrophotometry3, voltammetry4, titrimetric method5, biosensor6 and so on, Each method has its merits and defects in analyzing different samples. M. Petersson7 worked out the potentiometric sensor for determining ascorbic acid by modifying monolayer of ferrocene upon the surface of half-oxidized platinum electrode with an average response slope 50±8.8mV/decade, but this sensor suffers from inadequate selectivity. In our study, carbon paste electrode (without ionophore) is applied in the determination of ascorbic acid by potentiometry with an average response slope 95mV/decade. This method displays fine selectivity, accuracy, convenience and rapidity of determination.