首页> 外文期刊>International journal of environmental analytical chemistry >Mercury determination in sediments by CVAAS after on line preconcentration by solid phase extraction with a sol-gel sorbent containing CYANEX 471X®
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Mercury determination in sediments by CVAAS after on line preconcentration by solid phase extraction with a sol-gel sorbent containing CYANEX 471X®

机译:在线预浓缩后,使用包含CYANEX471X®的溶胶-凝胶吸附剂进行固相萃取,通过CVAAS测定沉积物中的汞

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The development of a preconcentration method for the measurement of trace levels of mercury in digested sediments is described. Solid phase extraction (SPE) was used for the preconcentration of mercury coupled on-line by means of a flow injection (FI) system followed by cold vapour atomic absorption spectrometry (CVAAS) detection. The SPE was carried out through a column packed with a sorbent material containing triisobutylphosphine sulfide (CYANEX 47IX®) as mercury extractant and prepared by the sol-gel process. The effects of FI variables (argon, eluent, and reductant flow rates, loading and elution times) as well as the eluent concentration on the analytical performance of the method were evaluated. The proposed method was validated under the optimum conditions. The calibration graph was linear from 0.05 μgL~(-1) to 3.0 μgL~(-1) of Hg. The detection limit (DL), based on three times the standard deviation of the blank measurement criterion, was 24ngL~(-1) The repeatability was 1.5% and 1.8% RSD (n= 10) at concentrations of 0.5 and 1 μgL~(-1) of Hg, respectively. Method enrichment factors of 16 with a productivity of 30 samples h~(-1) or 32 with a productivity of 17 samples h~(-1) were achieved under selected conditions. Certified reference materials, inductively coupled plasma mass spectroscopy (ICP-MS) and cold vapour atomic fluorescence spectrometry (CVAFS), were used to evaluate the accuracy of the proposed method.
机译:描述了一种用于测量消化沉积物中痕量汞的预浓缩方法的发展。固相萃取(SPE)用于通过流动注射(FI)系统随后冷蒸气原子吸收光谱(CVAAS)检测对在线耦合的汞进行预浓缩。通过填充有包含三异丁基膦硫醚(CYANEX47IX®)作为汞萃取剂的吸附剂材料的柱子进行SPE,并通过溶胶-凝胶法制备。评估了FI变量(氩气,洗脱液和还原剂流速,上样时间和洗脱时间)以及洗脱液浓度对方法分析性能的影响。该方法在最佳条件下得到了验证。校准曲线在0.05μgL〜(-1)至3.0μgL〜(-1)Hg之间呈线性关系。基于空白测量标准的三倍标准偏差的检出限(DL)为24ngL〜(-1)在0.5和1μgL〜(浓度)下的重复性分别为1.5%和1.8%RSD(n = 10)。 -1)的汞。在所选条件下,方法富集因子达到16个,生产率为30个样本h〜(-1)或32个,生产率为17个样本h〜(-1)。经认证的参考材料,电感耦合等离子体质谱法(ICP-MS)和冷蒸气原子荧光光谱法(CVAFS),用于评估该方法的准确性。

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