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胶束增溶-H 点标准加入分光光度法同时测定铁和钒

Simultaneous spectrophotometric determination of iron and vanadium by H-point standard addition method and partial least squares regression in micellar medium.

机构信息

Department of Chemistry, Institute for Advanced studies in Basic Sciences, Gava Zang, Zanjan 45195 159, Iran.

出版信息

Talanta. 2003 May 1;59(6):1141-51. doi: 10.1016/S0039-9140(03)00025-0.

Abstract

Simultaneous determination of total iron and vanadium by H-point standard addition method (HPSAM) and partial least squares (PLS) is described. Gallic acid (GA) in a cationic micellar solution of CTAB was used for determination of iron and vanadium in different oxidation states at pH 5. The presence of a micellar system enables total iron and vanadium to be determined with improved sensitivities. The total relative standard error for applying the PLS method to 15 synthetic samples in the ranges 0.20-15.00 mug ml(-1) iron and 0.20-8.00 mug ml(-1) vanadium was 2.2%. The results of applying the H-point standard addition method showed that iron and vanadium can be determined simultaneously with the concentration ratios of iron to vanadium from 10:1 to 1:20 in the mixed sample. Both HPSAM and PLS methods showed suitable abilities to resolve accurately overlapped absorption spectra of the compounds. Both proposed methods were successfully applied to the determination of Fe and V in several synthetic alloy solutions.

摘要

本文描述了利用 H 点标准加入法(HPSAM)和偏最小二乘法(PLS)同时测定总铁和钒的方法。在 CTAB 的阳离子胶束溶液中使用没食子酸(GA)在 pH 5 下测定不同价态的铁和钒。胶束体系的存在使总铁和钒的测定具有更高的灵敏度。将 PLS 法应用于 15 个合成样品的范围为 0.20-15.00μg ml(-1)铁和 0.20-8.00μg ml(-1)钒时,总相对标准误差为 2.2%。应用 H 点标准加入法的结果表明,在混合样品中,铁和钒的浓度比可以从 10:1 到 1:20 同时测定。HPSAM 和 PLS 两种方法均能准确分辨化合物的重叠吸收光谱,具有合适的分辨能力。两种方法均成功地应用于几种合成合金溶液中 Fe 和 V 的测定。

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