首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Spectrophotometric determination of trace lead in water after preconcentration using mercaptosephadex
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Spectrophotometric determination of trace lead in water after preconcentration using mercaptosephadex

机译:巯基葡聚糖凝胶分光光度法测定水中痕量铅。

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A highly sensitive and selective spectrophotometric method for determination of trace lead in water after pre-concentration using mercaptosephadex(MS-50) has been developed the method based on the colorreaction of lead (II) with dibromohydroxylphenylporphyrin.Under optimal condition leas(II) reacts with the reagent to form a 1:2 yellow comples in presence of TRITONx-100 which has a maximum absorption peak at 479 nm The color reaction can complete rapidly and remain stable for 24 h in room temperature.The molar absorption coefficient of the lead complex the limit of quantification the limit of detection and relative standard deviations were found to be 2.35 x 10~5 1 mol~-1 cm~-1 4.3,1.4 ng ml~-1 and 1.0% respectively The absorbance of the lead complex at 478 nm is linear up to 0.48 mug ml~-1 of lead(II) The effect of various co-existing ions in water were examined seriously No interference was observed.Moreover a simple pre-concentration method for trace lead in water were examined seriously.No interference was observed.Moreover a simple pre-concentration method for tarace lead in water can be adsorbed in 1.0 mol 1~-1 HCl and dissociated from MS-50 It was found that trace lead in water can be adsorbed in 1.0 mol 1~-1 HCl and sissociated from MS-50 with 4.0 mol 1~-1 HCl quantitatively that improves the selectivity and the sensitivity of method(its detection limit (3 s_ changed into 0.2 ng ml~-1 of lead) obviously.The proposed method had been applied to determine trace lead in water samples with satisfactory results.
机译:建立了基于巯基葡聚糖(MS-50)富集的高灵敏度选择性分光光度法测定水中痕量铅的方法,该方法基于铅(II)与二溴羟苯基卟啉的显色反应。在最佳条件下,leas(II)反应在TRITONx-100存在下,该试剂与试剂形成1:2的黄色化合物,在479 nm处具有最大吸收峰。显色反应可快速完成并在室温下保持稳定24 h。定量限检出限和相对标准偏差分别为2.35 x 10〜5 1 mol〜-1 cm〜-1 4.3、1.4 ng ml〜-1和1.0%铅配合物在478处的吸光度直到0.48毫升/毫升铅为止,nm都是线性的(II)认真检查了水中各种共存离子的影响未观察到干扰,此外还对水溶液中痕量铅的一种简单的预富集方法进行了研究此外,没有观察到干扰物。此外,一种简单的富集水中铅的预富集方法可以在1.0 mol 1〜-1 HCl中吸附并从MS-50上解离,发现水中的痕量铅可以在1.0 mol中吸附。 1〜-1 HCl和MS-50与4.0 mol 1〜-1 HCl定量缔合,提高了方法的选择性和灵敏度(其检测限(3 s_变为0.2 ng ml〜-1的铅)。将该方法用于水样中痕量铅的测定,结果令人满意。

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