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去除阳离子和阴离子干扰后,通过一氟化铝分子吸收光谱法测定海水中的氟化物。

Determination of fluoride in sea-water by molecular absorption spectrometry of aluminium monofluoride after removal cation and anion interferences.

作者信息

Corvillo M A, Gomez M G, Rica C C

机构信息

Departamento de Química Analítica, Facultad de Ciencias, Ciudad Universitaria, Universidad Complutense, Madrid 28040, Spain.

出版信息

Talanta. 1990 Jul;37(7):719-24. doi: 10.1016/0039-9140(90)80100-t.

Abstract

Three procedures are proposed for the determination of trace levels of fluoride in sea-water, based on the formation of aluminium monofluoride in an electrothermal graphite furnace, followed by measurement of its molecular absorption at 227.45 nm. They involve the use of dilution, a matrix modifier, or a matrix modifier and an ion-exchange resin, and are all acceptably sensitive and specific for fluoride. Interferences from cations and anions are removed by a simple 20-fold dilution of the sample. At 10-fold sample dilution, chloride interference can be removed by adding 0.3M ammonium nitrate together with 0.01M aluminium + 0.01M strontium as a matrix modifier. The same matrix modifier is valid for use with 5-fold sample dilution and a cation-exchange step to avoid matrix affects from cations and chloride. The detection limit is about 8-10 ng/ml fluoride and the determination limit is 20 ng/ml. The precision of peak-height measurement at 0.2 mug/ml is 5-7%.

摘要

提出了三种测定海水中痕量氟化物的方法,这些方法基于在电热石墨炉中形成一氟铝,随后测量其在227.45nm处的分子吸收。它们涉及使用稀释、基体改进剂或基体改进剂与离子交换树脂,并且对于氟化物而言都具有可接受的灵敏度和特异性。通过对样品进行简单的20倍稀释可消除阳离子和阴离子的干扰。在10倍样品稀释时,通过添加0.3M硝酸铵以及0.01M铝+0.01M锶作为基体改进剂可消除氯化物的干扰。相同的基体改进剂适用于5倍样品稀释以及阳离子交换步骤,以避免阳离子和氯化物的基体影响。检测限约为8-10ng/ml氟化物,测定限为20ng/ml。在0.2μg/ml时峰高测量的精密度为5-7%。

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