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Study on Speciation of As Cr and Sb in Bottled Flavored Drinking Water Samples Using Advanced Analytical Techniques IEC/SEC-HPLC/ICP-DRC-MS and ESI-MS/MS

机译:使用高级分析技术IEC / SEC-HPLC / ICP-DRC-MS和ESI-MS / MS研究瓶装风味饮用水样品中AsCr和Sb的形态

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摘要

The main aim of the research was to develop a complementary analytical approach consisting of bespoke speciation analysis and non-targeted speciation analysis of As, Sb, and Cr in flavored bottled drinking water samples using HPLC/ICP-DRC-MS and ESI-MS/MS. The scope of two previously developed analytical procedures, (1) multielemental speciation procedure for AsIII, AsV, CrVI, SbIII, and SbV analysis and (2) arsenic speciation procedure for AsB, AsIII, DMA, MMA, and AsV quantification, was extended to the analysis of a new sample type in terms of bespoke speciation analysis. As for the non-targeted speciation, analysis size exclusion chromatography was used with ICP-MS and a complementary technique, ESI-MS/MS, was used for the organic species of As, Sb, and Cr screening. Full validation of procedures 1 and 2 was conducted. Procedure 1 and 2 were characterized with precision values in the range from 2.5% to 5.5% and from 3.6% to 7.2%, respectively. Obtained recoveries ranged from 97% to 106% and from 99% to 106% for procedures 1 and 2, respectively. Expanded uncertainties calculated for procedures 1 and 2 ranged from 6.1% to 9.4% and from 7.4% to 9.9%, respectively. The applicability of the proposed procedures was tested on bottled drinking water samples. Results for the real samples in procedure 1 were in the range from 0.286 ± 0.027 [μg L−1] to 0.414 ± 0.039 [μg L−1] for AsIII, from 0.900 ± 0.083 [μg L−1] to 3.26 ± 0.30 [μg L−1] for AsV, and from 0.201 ± 0.012 [μg L−1] to 0.524 ± 0.032 [μg L−1] for SbV. CrVI and SbIII were not detected in any sample. As for procedure 2, results were in the range from 0.0541 ± 0.0053 [μg L−1] to 0.554 ± 0.054 [μg L−1] for AsB. Results for AsIII and AsV obtained with procedure 2 were in good accordance with results obtained with procedure 1. DMA and MMA were not detected in any sample.
机译:该研究的主要目的是开发一种互补的分析方法,包括使用HPLC / ICP-DRC-MS和ESI-MS /进行定制的形态分析和风味瓶装饮用水样品中的As,Sb和Cr的非目标形态分析。多发性硬化症。以前开发的两种分析程序的范围:(1)As III ,As V ,Cr VI ,Sb 的多元素物种形成程序III 和Sb V 分析以及(2)AsB,As III ,DMA,MMA和As V 量化,已根据定制形态分析扩展到新样品类型的分析。至于非目标物种,则采用ICP-MS分析尺寸排阻色谱法,并将辅助技术ESI-MS / MS用于As,Sb和Cr的有机物筛选。进行了程序1和2的完全验证。程序1和2的精度分别在2.5%至5.5%和3.6%至7.2%范围内。步骤1和步骤2的回收率分别为97%至106%和99%至106%。为程序1和2计算的扩展不确定度分别为6.1%至9.4%和7.4%至9.9%。建议的程序的适用性在瓶装饮用水样品上进行了测试。步骤1中真实样品的结果在As -1 ]到0.414±0.039 [μgL -1 ] > III ,对于As V -1 ]到3.26±0.30 [μgL -1 ] >,Sb V 的范围从0.201±0.012 [μgL -1 ]到0.524±0.032 [μgL -1 ]。样品中均未检出Cr VI 和Sb III 。对于步骤2,对于AsB,结果范围为0.0541±0.0053 [μgL -1 ]至0.554±0.054 [μgL -1 ]。步骤2获得的As III 和As V 的结果与步骤1获得的结果完全一致。在任何样品中均未检测到DMA和MMA。

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