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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Determination of iron(III) in water samples by microsequential injection solid phase spectrometry using an hexadentate 3-hydroxy-4-pyridinone chelator as reagent
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Determination of iron(III) in water samples by microsequential injection solid phase spectrometry using an hexadentate 3-hydroxy-4-pyridinone chelator as reagent

机译:通过使用六向三羟基-4-吡啶酮螯合剂作为试剂,通过微饱和3-羟基-4-吡啶酮螯合剂测定水样中的铁(III)在水样中的测定

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摘要

In this work, the hexadentate 3,4–hydroxypyridinone ligand was used as reagent for the spectrophotometric quantification of iron(III) in fresh and sea waters, using a micro sequential injection lab-on-valve (μSI-LOV) system in a solid phase spectrometry (SPS) mode. To implement SPS, thus eliminating the sample matrix, a packed column in the flow cell was used; the chosen sorbent was Nitrilotriacetic Acid Superflow resin (NTA). The possibility of performing an analytical curve resorting to just one standard was also demonstrated. The consumption of the hexadentante ligand was about 30?μg per determination and the effluent production lower than 2.5?mL. The dynamic concentration range was 0.45–9.0?μmol?L?1, with a limit of detection of 0.13?μmol?L?1and limit of quantification 0.43?μmol?L?1. The proposed μSI-LOV-SPS methodology was successfully applied to river, ground, estuarine, tap, and sea waters.
机译:在这项工作中,使用固体微链注射实验室(μSI-LOV)系统,用作新鲜和海水中铁(III)的分光光度量化的试剂,以便固体 相位光谱(SPS)模式。 为了实现SPS,从而消除了样品矩阵,使用了流动单元中的填充柱; 所选择的吸附剂是硝基酰基乙酸超流树脂(NTA)。 还证明了进行分析曲线诉诸只有一个标准的可能性。 每种测定和氟化物的消耗约为30μg,流出物产生低于2.5×mL。 动态浓度范围为0.45-9.0?μmol?1,检测极限为0.13Ωμmol?l?1和量子限制0.43≤μmol?1。 提出的μSI-Lov-SPS方法已成功应用于河流,地面,河口,水龙头和海水。

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