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2011•Collection of Czechoslovak Chemical CommunicationsRequires access

Voltammetric determination of 1,2-diaminoanthraquinone using carbon paste electrode

Jiřı́ Zima, Veronika Tinková, Joseph Wang, Jiřı́ Barek

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Abstract

Direct current (DC) voltammetry and differential pulse (DP) voltammetry using a carbon paste electrode (CPE) have been used for the determination of trace amounts of ecotoxic 1,2-diaminoanthraquinone (DAAQ). The limit of determination (LD) of DAAQ for DC voltammetry was 2 × 10–6 mol l–1, and for DP voltammetry 2 × 10–7 mol l–1 under the optimized conditions in a mixed Britton–Robinson buffer pH 12 and methanol (1:9) medium. Adsorptive accummulation of the analyte on the surface of CPE decreased the limit of determination to 2 × 10–8 mol l–1 for DP voltammetry. Practical applicability of these newly developed methods was verified on model samples of river water.

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What this paper is about

Direct current (DC) voltammetry and differential pulse (DP) voltammetry using a carbon paste electrode (CPE) have been used for the determination of trace amounts of ecotoxic 1,2-diaminoanthraquinone (DAAQ). The limit of determination (LD) of DAAQ for DC voltammetry was 2 × 10–6 mol l–1, and for DP voltammetry 2 × 10–7 mol l–1 under the optimized conditions in a mixed Britton–Robinson buffer pH 12 and methanol (1:9) medium. Adsorptive accummulation of the analyte on the surface of CPE decreased the limit of determination to 2 × 10–8 mol l–1 for DP voltammetry. Practical applicability of these newly developed methods was verified on model samples of river water.

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Available abstract

Direct current (DC) voltammetry and differential pulse (DP) voltammetry using a carbon paste electrode (CPE) have been used for the determination of trace amounts of ecotoxic 1,2-diaminoanthraquinone (DAAQ). The limit of determination (LD) of DAAQ for DC voltammetry was 2 × 10–6 mol l–1, and for DP voltammetry 2 × 10–7 mol l–1 under the optimized conditions in a mixed Britton–Robinson buffer pH 12 and methanol (1:9) medium. Adsorptive accummulation of the analyte on the surface of CPE decreased the limit of determination to 2 × 10–8 mol l–1 for DP voltammetry. Practical applicability of these newly developed methods was verified on model samples of river water.

Key concepts: Differential pulse voltammetry, Voltammetry, Detection limit, Carbon paste electrode, Cyclic voltammetry, Analytical Chemistry (journal), Chemistry, Analyte

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