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采用 8-羟基喹啉-钴(II)共沉淀体系预浓缩、分离和分光光度法测定水样和透析浓缩物中的痕量铝(III)。

Preconcentration, separation and spectrophotometric determination of aluminium(III) in water samples and dialysis concentrates at trace levels with 8-hydroxyquinoline-cobalt(II) coprecipitation system.

机构信息

Maçka Vocational School, Karadeniz Technical University, 61750 Trabzon, Turkey.

出版信息

J Hazard Mater. 2010 Oct 15;182(1-3):331-6. doi: 10.1016/j.jhazmat.2010.06.034. Epub 2010 Jun 16.

DOI:10.1016/j.jhazmat.2010.06.034
PMID:20619964
Abstract

A separation-preconcentration procedure was developed for the determination of trace amounts of aluminium in water samples and dialysis concentrates by UV-vis Spectrophotometry after coprecipitation using 8-hydroxyquinoline (8-HQ) as a chelating agent and Co(II) as a carrier element. This procedure is based on filtration of the solution containing precipitate on a cellulose nitrate membrane filter following aluminium(III) coprecipitation with Co/8-HQ and then the precipitates together with membrane filter were dissolved in concentrated nitric acid. The metal contents of the final solution were determined by UV-vis Spectrophotometry with Erio Chrome Cyanine-R standard method. Several parameters including pH of sample solution, amount of carrier element and reagent, standing time, sample volume for precipitation and the effects of diverse ions were examined. The enrichment factor was calculated as 50 and the detection limits, corresponding to three times the standard deviation of the blank (N: 10), was found to be 0.2 microg L(-1). The accuracy of the method was tested with standard reference material (CRM-TMDW-500) and spiked addition. Determination of aluminium(III) was carried out in sea water, river water, tap water and haemodialysis fluids samples. The recoveries were >95%. The relative standard deviations of determination were less than 6%.

摘要

建立了一种采用 8-羟基喹啉(8-HQ)作为螯合剂,Co(II)作为载体元素共沉淀分离富集,然后用纤维素硝酸酯膜过滤,滤液经浓硝酸溶解,用可见分光光度法测定水样和透析浓缩液中痕量铝的方法。实验考察了溶液 pH 值、载带元素和试剂用量、陈化时间、沉淀体积以及共存离子的影响。该方法的富集倍数为 50,检测限(空白 10 次测定的 3 倍标准偏差)为 0.2μg/L。以标准参考物质(CRM-TMDW-500)和加标回收实验对方法的准确性进行了验证,铝的回收率大于 95%,相对标准偏差小于 6%。该方法用于海水、河水、自来水和血液透析液中铝的测定。

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