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离子色谱法测定水中无机阴离子:一项协同研究。

Determination of inorganic anions in water by ion chromatography: a collaborative study.

作者信息

Edgell K W, Longbottom J E, Pfaff J D

机构信息

Bionetics Corp., Cincinnati, OH 45246.

出版信息

J AOAC Int. 1994 Sep-Oct;77(5):1253-63.

PMID:7950425
Abstract

The U.S. Environmental Protection Agency (U.S. EPA) and the American Society for Testing and Materials (ASTM) conducted a joint collaborative study validating an ion chromatographic method for determination fo inorganic anions (U.S. EPA method 300.0A and the equivalent proposed revision to ASTM method D4327). This study was conducted to determine the mean recovery and precision of analyses for bromide, chloride, fluoride, nitrate, nitrite, orthophosphate, and sulfate in reagent water, drinking water, and wastewater. The study design was based on Youden's nonreplicate plan for collaborative tests of analytical methods. The test waters were spiked with the anions at 6 concentration levels, prepared as 3 Youden pairs. The 22 volunteer laboratories were instructed to dilute 10 mL sample concentrate to 100 mL test water. A measured volume of sample (20-200 microL) was injected into an ion chromatograph equipped with a guard column, anion exchange column, and a chemical micromembrane suppression device. The anions were then separated using 1.7 mM sodium bicarbonate and 1.8 mM sodium carbonate, and measured by a conductivity detector. Submitted data were evaluated using U.S. EPA's IMVS computer program, which follows ASTM D2777-86 statistical guidance. U.S. EPA method 300.0A and ASTM method D4327 were judged acceptable for measurement of the above anions (except sulfate) at concentrations ranging from 0.3 to 25 mg/L and sulfate concentrations from 2.9 to 95 mg/L. Mean recoveries for the 7 anions from all matrixes, as estimated from the linear regression equations, ranged from 95 to 104%. At concentrations above 2-6 mg/L for bromide, fluoride, nitrate, nitrite, and orthophosphate, and above 24 mg/L for sulfate, the overall and single-analyst relative standard deviations were less than 10 and 6%, respectively. As concentrations decreased, precision became more variable. The relative standard deviations of results for chloride were slightly higher than the other anions, especially in matrixes with high chloride background. Analysis of Variance (ANOVA) tests at the 95% confidence interval indicated a statistically significant matrix effect for chloride, nitrite, and nitrate analyses in drinking water compared to analyses in reagent water. Because these matrix effects were caused by the spiking process and not the drinking water itself, the ANOVA determination was not considered to be of practical significance.

摘要

美国环境保护局(U.S. EPA)和美国材料与试验协会(ASTM)开展了一项联合协作研究,以验证一种用于测定无机阴离子的离子色谱法(U.S. EPA方法300.0A以及ASTM方法D4327的等效拟修订版)。开展这项研究是为了确定在试剂水、饮用水和废水中溴化物、氯化物、氟化物、硝酸盐、亚硝酸盐、正磷酸盐和硫酸盐分析的平均回收率和精密度。研究设计基于尤登(Youden)非重复分析方法协作试验方案。测试水样添加了6种浓度水平的阴离子,配制成3对尤登对。指导22个志愿实验室将10 mL样品浓缩液稀释至100 mL测试水。将一定体积的样品(20 - 200微升)注入配备了保护柱、阴离子交换柱和化学微膜抑制装置的离子色谱仪。然后使用1.7 mM碳酸氢钠和1.8 mM碳酸钠分离阴离子,并通过电导检测器进行测量。使用遵循ASTM D2777 - 86统计指南的U.S. EPA的IMVS计算机程序对提交的数据进行评估。U.S. EPA方法300.0A和ASTM方法D4327被判定可接受用于测量浓度范围为0.3至25 mg/L的上述阴离子(硫酸盐除外)以及浓度范围为2.9至95 mg/L的硫酸盐。根据线性回归方程估算,所有基质中7种阴离子的平均回收率在95%至104%之间。对于溴化物、氟化物、硝酸盐、亚硝酸盐和正磷酸盐,当浓度高于2 - 6 mg/L时,以及对于硫酸盐,当浓度高于24 mg/L时,总体相对标准偏差和单分析师相对标准偏差分别小于10%和6%。随着浓度降低,精密度变得更具变化性。氯化物结果的相对标准偏差略高于其他阴离子,尤其是在氯化物背景较高的基质中。在95%置信区间进行的方差分析(ANOVA)测试表明,与试剂水分析相比,饮用水中氯化物、亚硝酸盐和硝酸盐分析存在统计学上显著的基质效应。由于这些基质效应是由加标过程引起的,而非饮用水本身,因此方差分析的结果被认为不具有实际意义。

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