Behaviour of chemical modifiers in the determination of arsenic by electrothermal atomic absorption spectrometry in petroleum products

被引:24
|
作者
Reboucas, MV
Ferreira, SLC
Neto, BD
机构
[1] Braskem SA, Unidade Insumos Basicos, Lab, BR-42810000 Camacari, BA, Brazil
[2] Univ Fed Bahia, Inst Quim, Dept Quim Analit, BR-40170290 Salvador, BA, Brazil
[3] Univ Fed Pernambuco, Dept Quim Fundamental, BR-50740540 Recife, PE, Brazil
关键词
chemical modifier; arsenic; naphtha; petroleum condensate; ETAAS; Doehlert;
D O I
10.1016/j.talanta.2005.02.014
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Most comparative studies on the efficiency of chemical modifiers have been conducted in aqueous media. In the present work, we proposed a detailed study of the use of different chemical modifiers for direct determination of arsenic in complex organic matrices by electrothermal atomic absorption spectrometry (ETAAS). Palladium, rhodium, tungsten, silver, lanthanum and a mixture of palladium and magnesium were tested. The figures of merit used for evaluation and comparison were acquired in the optimal conditions for each modifier, established by multivariate optimization of the main variables based on Doehlert designs. Singular features were observed for the chemical behaviour of some modifiers in organic matrices compared to aqueous media, such as the worse performance of Pd + Mg modifier and no notice of severe tube corrosion from La application. Lanthanum was chosen as the best chemical modifier for the present application, according to predefined criteria. Lanthanum showed the minimum limit of detection, characteristic concentration and blank signal among all tested species and no effect of the concomitants usually present in petrochemical feedstocks. Using a 200 mg L-1 lanthanum solution as a chemical modifier, the average relative standard deviations of 7 and 16% (at 3-15 mu g L-1 level) and characteristic concentrations of 0.47 and 0.77 mu g L-1 for naphtha and petroleum condensates, respectively, were observed. (C) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:195 / 204
页数:10
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