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Comparative study of three methods for the analysis of nitrate nitrogen in synthetic water and wastewater samples

机译:三种合成水和废水中硝酸盐氮分析方法的比较研究

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Measurement of nitrate nitrogen is relatively less easy and reliable, given the complexity of analytical procedures already marred by interferences. Interfering constituents like organics are frequently integral to the nature of the samples. As a result, in practice nitrate nitrogen () concentrations often go under-/over-reported. Objective of this study was to compare three analytical procedures extensively used for determination of , namely Ultraviolet Spectrophotometric Screening (UV) Method, Nitrate Electrode Method (Ion-Electrode method) and Phenol Disulphonic Acid (PDA) Method. Usually, these methods of nitrate measurement are commonly employed based on availability of analytical facilities rather than the characteristics of the samples that carry many constituents other than nitrates also, which can limit their application in certain cases. The paper can help serve as a guide to method selection. Comparative investigation on the basis of Passing-Bablok and Bland-Altman analyses showed that when samples had no organics, the accuracy of the three methods was in the order: UV > PDA > Ion-Electrode. Ion-Electrode method was found to be affected by a positive bias of 0.799 for a confidence interval of (0.161, 1.436). For samples containing organics, all three methods were affected by proportional bias. UV method was most affected by interference, exhibiting a bias, regression intercept and slope coefficient of -1.733, -1.359 and 0.922, respectively. Interference due to organics was further analysed experimentally and accuracy with respect to rising organic concentration was found to be in the order: UV < Ion-Electrode < PDA, i.e. PDA method gave least percentage error for high organic concentrations. Multiple linear regression (MLR) models were developed for predicting more accurate readings. MLR models based on two and four explanatory variables for PDA (R-2 = 92.86%, predicted R-2 = 91.33%) and UV method (R-2 = 99.87%, predicted R-2 = 99.83%) respectively are reported.
机译:鉴于干扰已经损害了分析程序的复杂性,硝酸盐氮的测量相对较不容易和可靠。干扰成分(如有机物)通常是样品性质不可或缺的组成部分。结果,实际上,硝酸盐氮()的浓度经常被低估/高估。本研究的目的是比较广泛用于测定的三种分析程序,即紫外分光光度筛选(UV)方法,硝酸盐电极方法(离子电极方法)和苯酚二磺酸(PDA)方法。通常,这些硝酸盐测量方法通常是根据分析设备的可用性而采用的,而不是基于样本中除了硝酸盐以外还包含许多其他成分的特性,这在某些情况下会限制其应用。本文可以帮助您选择方法。在Passing-Bablok和Bland-Altman分析的基础上进行的比较研究表明,当样品不含有机物时,这三种方法的准确度依次为:UV> PDA>离子电极。发现离子电极方法受0.799的正偏差影响,置信区间为(0.161,1.436)。对于包含有机物的样品,这三种方法均受比例偏差的影响。 UV方法受干扰影响最大,其偏度,回归截距和斜率系数分别为-1.733,-1.359和0.922。实验进一步分析了由有机物引起的干扰,发现有机物浓度升高的准确度按以下顺序排列:UV <离子电极

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