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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Rapid determination of lead extracted by acetic acid from glazed ceramic surfaces by flow injection on-line preconcentration and spectrophotometric detection
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Rapid determination of lead extracted by acetic acid from glazed ceramic surfaces by flow injection on-line preconcentration and spectrophotometric detection

机译:流动注射在线预富集和分光光度法快速测定乙酸从釉面陶瓷表面提取的铅

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摘要

A. rapid method has been developed for the determination of lead extracted by acetic acid from glazed ceramic surfaces by flow injection analysis without any pretreatment. An aliquot of 4% acetic acid solution, which has been kept in a teacup for 24 h in the dark, is injected into a carrier solution (1 M nitric acid) and passed through a Pb-Spec resin column. After washing the column with an ammonium nitrate solution, the lead adsorbed on the column is eluted with an ammonium oxalate solution and then merged with a 4-(2-pyridylazo)resorcinol (PAR) solution, followed by measurement of the absorbance of the lead-PAR complex at 530 nm. The detection limit, concentration giving a signal equal to three times the standard deviation of the blank signal, is 8 ng ml(-1). The relative standard deviation of measurements at the 0.8 mu g ml(-1) level is 0.35% (n=5). The sample throughput is 12 per hour. (c) 2005 Elsevier B.V. All rights reserved.
机译:已经开发出一种快速方法,用于通过流动注射分析无需任何预处理即可测定乙酸从釉面陶瓷表面提取的铅。将等分的4%乙酸溶液在黑暗中于茶杯中放置24小时,然后将其注入载液(1 M硝酸)中,并通过Pb-Spec树脂柱。用硝酸铵溶液洗涤色谱柱后,用草酸铵溶液洗脱吸附在色谱柱上的铅,然后与4-(2-吡啶基偶氮)间苯二酚(PAR)溶液合并,然后测量铅的吸光度-PAR复合物在530 nm处。给出信号强度等于空白信号标准偏差三倍的浓度的检测极限为8 ng ml(-1)。在0.8μg ml(-1)浓度下的相对测量标准偏差为0.35%(n = 5)。样品通量为每小时12个。 (c)2005 Elsevier B.V.保留所有权利。

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