Araújo M C, Santos A V, Honorato R S, Pasquini C
Departamento de Química, CCEN Universidade Federal da Paraíba C.P. 5093 João Pessoa PB 58051-970 Brazil.
J Automat Chem. 1997;19(5):157-64. doi: 10.1155/S1463924697000163.
This paper describes use of gradients of concentration generated in flow injection (FI) systems to perform determinations based on points where the concentration of titrant and analyte are at stoichiometric ratio. Two procedures were developed. In one procedure the titrant is injected in a FI manifold and merges with the sample which is continuously pumped towards the detector. In the other procedure the sample is injected and merged with the titrant which is continuously pumped. Both techniques make use of concentration gradients of the sample or titrant generated in FI manifolds that contain a mixing chamber. This gradient is calibrated employing only one standard solution (usually the titrant) in order to convert any detector signal, obtained in the elapsed time after injection, to instantaneous concentration values. The flow system is microcomputer controlled and data are treated to locate points where the concentration of titrant and analyte are at the stoichiometric ratio. These points are found in abrupt changes of the signal x concentration curves obtained in the presence of the reaction. The method has been evaluated for determination of Fe(II) and acetic acid by spectrophotometric and conductimetric detection, respectively. Results show a mean relative standard deviation lower than 1%, an average accuracy of 1% and a high sampling processing capability (40 to 60 samples per hour).
本文描述了利用流动注射(FI)系统中产生的浓度梯度,基于滴定剂和分析物浓度处于化学计量比的点进行测定。开发了两种方法。在一种方法中,将滴定剂注入FI流路中,并与连续泵送至检测器的样品合并。在另一种方法中,注入样品并与连续泵送的滴定剂合并。这两种技术都利用了包含混合室的FI流路中产生的样品或滴定剂的浓度梯度。仅使用一种标准溶液(通常是滴定剂)对该梯度进行校准,以便将注射后经过的时间内获得的任何检测器信号转换为瞬时浓度值。流动系统由微型计算机控制,并对数据进行处理以定位滴定剂和分析物浓度处于化学计量比的点。这些点出现在反应存在时获得的信号x浓度曲线的突变处。该方法已分别通过分光光度法和电导检测法对Fe(II)和乙酸的测定进行了评估。结果表明,平均相对标准偏差低于1%,平均准确度为1%,且具有较高的进样处理能力(每小时40至60个样品)。