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首页> 外文期刊>Analytical Letters >Sequential Injection On-Line Sorption Preconcentration Using PEEK-Turnings Packed Micro-Column for Ultra-Trace Cobalt Determination by Electrothermal Atomic Absorption Spectrometry
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Sequential Injection On-Line Sorption Preconcentration Using PEEK-Turnings Packed Micro-Column for Ultra-Trace Cobalt Determination by Electrothermal Atomic Absorption Spectrometry

机译:PEEK-Turnings填充微柱顺序进样在线吸附富集-电热原子吸收光谱法测定痕量钴

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A novel sequential injection on-line column preconcentration method for ultra-trace cobalt determination by electrothermal atomic absorption spectrometry (ETAAS) using poly(etheretherketone) (PEEK) turnings as sorbent material was developed. The method was based on the on-line chelate complex formation and retention of target analyte with ammonium pyrrolidine dithiocarbamate (APDC) on the surface of PEEK-turnings and elution with methyl isobutyl ketone (MIBK). A 40 μL fraction of MIBK containing the bulk of analyte complex introduced directly into the transversely heated graphite tube atomizer of ETAAS for quantification. Acidity of sample solution, chelating reagent concentration, and preconcentration time were investigated and optimized separately, while all other factors were optimized by full factorial design optimization methodology. The significance of the variables and their interactions was estimated by employing analysis of variance (ANOVA) and Pareto chart. Under the optimum conditions the enhancement factor for cobalt determination was 60. The detection limit was 6 ng L ~(-1) and the precision expressed as relative standard deviation (RSD) was 3.5% at 0.1 μg L ~(-1) Co(II) concentration level, respectively. The proposed method was evaluated by analyzing water certified reference materials and spiked environmental samples.
机译:提出了一种以聚醚醚酮(PEEK)为吸附剂的电热原子吸收光谱法(ETAAS)测定痕量钴的连续进样在线柱富集新方法。该方法基于在线螯合物的形成和目标分析物与吡咯烷二硫代氨基甲酸铵(APDC)在PEEK车削表面上的保留并用甲基异丁基酮(MIBK)洗脱。 40μL的MIBK馏分包含直接引入ETAAS的横向加热石墨管雾化器中以进行定量的大部分分析物配合物。分别研究和优化了样品溶液的酸度,螯合剂浓度和预浓缩时间,同时通过全因子设计优化方法优化了所有其他因素。通过采用方差分析(ANOVA)和帕累托图来估计变量及其相互作用的重要性。在最佳条件下,钴测定的增强因子为60。检测限为6 ng L〜(-1),在0.1μgL〜(-1)Co(下限)下,以相对标准偏差(RSD)表示的精度为3.5%。 II)浓度水平。通过分析水认证的参考物质和加标的环境样品对提出的方法进行了评估。

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