首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >High performance liquid chromatography hydride generation in situ trapping graphite furnace atomic absorption: A new way of performing speciation analysis spectrometry using GFAAS as detector
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High performance liquid chromatography hydride generation in situ trapping graphite furnace atomic absorption: A new way of performing speciation analysis spectrometry using GFAAS as detector

机译:高效液相色谱法氢化物发生原位捕集石墨炉原子吸收:以GFAAS为检测器进行形态分析的新方法

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A new procedure for the speciation analysis of hydride forming elements using GFAAS as detector is proposed. The separation of the species is performed by HPLC and the eluent flow is merged with HCl and NaBH4 solutions moved by peristaltic pumps controlled by a flow injection apparatus. As the species emerges from the column, its respective hydride is formed and carried through the autosampler capillary to an Ir treated graphite tube pre-heated at 300 degrees C, where it is trapped. After the hydride collection, the autosampler arm is moved from the tube and atomization takes place. The sequence is repeated for the next emerging species. The feasibility of the system was evaluated for the speciation of As (111) and As (V) in waste water samples. The retention times were previously determined using a more concentrated mixed analytical solution and a quartz tube as atomizer. The analytical curves obtained by the proposed procedure showed similar slopes for both species as well as coefficient of regression better than 0.99. Limits of detection were 0.2 ng/mL for both species, 50 times better then the same assembly using a quartz tube atomizer. In the analysis of certified reference materials the sum of the As (111) and As (V) species concentrations were in close agreement with the arsenic concentration certified for total arsenic. (c) 2006 Elsevier B.V. All rights reserved.
机译:提出了一种以GFAAS为检测剂的氢化物形成元素形态分析的新方法。物种的分离通过HPLC进行,洗脱液流与HCl和NaBH4溶液合并,而HCl和NaBH4溶液由流量注入设备控制的蠕动泵移动。当物质从色谱柱中出来时,会形成其各自的氢化物,并通过自动进样器毛细管带入预先加热至300摄氏度的Ir处理过的石墨管中,并在其中捕集。收集氢化物后,将自动进样器臂从试管中移出并进行雾化。对下一个出现的物种重复该序列。评估了该系统用于废水样品中As(111)和As(V)形态的可行性。保留时间是使用更浓缩的混合分析溶液和石英管作为雾化器预先确定的。通过提出的程序获得的分析曲线显示出两种物种的相似斜率以及优于0.99的回归系数。两种物质的检出限均为0.2 ng / mL,比使用石英管雾化器的相同组件高50倍。在认证参比物质的分析中,As(111)和As(V)物种的浓度总和与总砷中认证的砷浓度高度吻合。 (c)2006 Elsevier B.V.保留所有权利。

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