Abstract
The aminated metal-organic framework H(2)N-MIL-101(Cr) was used as the carbon paste electrode (CPE) modifier for the determination of tartrazine (Tz) in soft drinks. The amino material was characterized by electrochemical impedance spectroscopy and showed significantly faster electron transfer with lower charge-transfer resistance (0.13 kΩ) compared to the electrode modified with the unfunctionalized MIL-101(Cr) material (1.1 kΩ). The H(2)N-MIL-101(Cr)-modified CPE [H(2)N-MIL-101(Cr)-CPE] was then characterized by cyclic voltammetry (CV) using [Fe(CN)(6)](3-) and [Ru(NH(3))(6)](3+) ions as the redox probes, showing good accumulation of [Fe(CN)(6)](3-) ions on the electrode surface. A CV scan of Tz in Britton Robinson buffer solution revealed an irreversible system with an oxidation peak at +0.998 V versus Ag/AgCl/KCl. Using CV and differential pulse voltammetry, an electrochemical method for quantifying Tz in aqueous medium was then developed. Several parameters that affect the accumulation and detection steps were optimized. Optimal detection of Tz was achieved after 180 s of accumulation in Britton Robinson buffer solution (pH 2) using 2 mg of H(2)N-MIL-101(Cr) material. Under optimal conditions, the sensor exhibited a linear response in the concentration range of 0.004-0.1 μM and good detection sensitivity (35.4 μA μM(-1)), and the detection limit for Tz was found to be 1.77 nM (S/N = 3). Satisfactory repeatability, stability, and anti-interference performance were also achieved on H(2)N-MIL-101(Cr)-CPE. The sensor was applied to commercial juices, and the results obtained were approximately similar to those given by UV-vis spectrophotometry.