CBQF/Escola Superior de Biotecnologia, Universidade Católica Portuguesa, Rua Dr. António Bernardino de Almeida, Porto, Portugal.
Talanta. 2010 Jun 15;81(4-5):1735-41. doi: 10.1016/j.talanta.2010.03.032. Epub 2010 Mar 25.
A multicommuted flow system with the propulsion device placed before detection is proposed for the determination of tartaric acid and free potassium in table and Port wines. A dialysis unit was introduced to increase sample dilution and minimize matrix interferences. The determination of tartaric acid was based on the spectrophotometric monitorization of the complex formed by the dialyzed analyte with vanadate. Potentiometric measurement of potassium was carried out through an ion selective tubular electrode. Dynamic linear ranges of 0.500-5.00gL(-1) and 390-2000mgL(-1) were achieved for tartaric acid and potassium determinations, respectively. Detection and quantification limits of 0.1 and 0.4gL(-1) of tartaric acid were obtained, respectively. For the potentiometric determination, a detection limit of 1x10(-4)molL(-1) was achieved. The accuracy of the method was assessed by analysis of 30 wine samples by the proposed methodology and manual procedures. There were no statistical differences between the 2 sets of results, in both determinations. Relative standard deviations lower than 2.1 and 2.4% were attained by the spectrophotometric and potentiometric measurements, respectively. A determination rate of 52h(-1) was achieved.
提出了一种在检测前放置推进装置的多交换流系统,用于测定葡萄酒和波特酒中的酒石酸和游离钾。引入了透析单元以增加样品稀释度并最小化基质干扰。酒石酸的测定基于与钒酸盐形成的被透析分析物的络合物的分光光度监测。通过离子选择性管状电极进行钾的电位测量。酒石酸和钾测定的动态线性范围分别为 0.500-5.00gL(-1)和 390-2000mgL(-1)。酒石酸的检测限和定量限分别为 0.1 和 0.4gL(-1)。对于电位测定,检测限达到 1x10(-4)molL(-1)。通过所提出的方法和手动程序对 30 个葡萄酒样品进行分析来评估方法的准确性。在这两种测定中,两组结果之间没有统计学差异。分光光度法和电位法的相对标准偏差分别低于 2.1%和 2.4%。测定速率达到 52h(-1)。