Galvis-Sánchez Andrea C, Santos João Rodrigo, Rangel António O S S
CBQF - Centro de Biotecnologia e Química Fina - Laboratório Associado, Escola Superior de Biotecnologia, Universidade Católica Portuguesa/Porto, Rua Dr. António Bernardino Almeida, 4200-072 Porto, Portugal.
CBQF - Centro de Biotecnologia e Química Fina - Laboratório Associado, Escola Superior de Biotecnologia, Universidade Católica Portuguesa/Porto, Rua Dr. António Bernardino Almeida, 4200-072 Porto, Portugal.
Talanta. 2015 Feb;133:1-6. doi: 10.1016/j.talanta.2013.12.058. Epub 2014 Jan 2.
A standard addition method was implemented by using a flow manifold able to perform automatically multiple standard additions and in-line sample treatment. This analytical strategy was based on the in-line mixing of sample and standard addition solutions, using a merging zone approach. The flow system aimed to exploit the standard addition method to quantify the target analyte particularly in cases where the analyte concentration in the matrix is below the lower limit of linear response of the detector. The feasibility of the proposed flow configuration was assessed through the potentiometric determination of fluoride in sea salts of different origins and different types of coffee infusions. The limit of quantification of the proposed manifold was 5×10(-6) mol L(-1), 10-fold lower than the lower limit of linear response of the potentiometric detector used. A determination rate of 8 samples h(-1) was achieved considering an experimental procedure based on three standard additions per sample. The main advantage of the proposed strategy is the simple approach to perform multiple standard additions, which can be implemented with other ion selective electrodes, especially in cases when the primary ion is below the lower limit of linear response of the detector.
采用一种能够自动进行多次标准加入和在线样品处理的流动歧管实施标准加入法。这种分析策略基于合并区方法,通过在线混合样品和标准加入溶液来实现。该流动系统旨在利用标准加入法对目标分析物进行定量,特别是在基质中分析物浓度低于检测器线性响应下限的情况下。通过电位法测定不同来源的海盐和不同类型咖啡冲泡液中的氟化物,评估了所提出的流动配置的可行性。所提出的歧管的定量限为5×10⁻⁶ mol L⁻¹,比所用电位检测器线性响应下限低10倍。考虑到每个样品基于三次标准加入的实验程序,实现了每小时8个样品的测定速率。所提出策略的主要优点是进行多次标准加入的方法简单,这可以与其他离子选择性电极一起实施,特别是在主要离子低于检测器线性响应下限的情况下。