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Determination of arsenic(III) and total inorganic arsenic in water samples using an on-line sequential insertion system and hydride generation atomic absorption spectrometry

机译:在线顺序插入系统和氢化物发生原子吸收光谱法测定水样中的砷(III)和总无机砷

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A simple and robust on-line sequential insertion system coupled with hydride generation atomic absorption spectrometry (HG-AAS) was developed,for selective As(III) and total inorganic arsenic determination without pre-reduction step.The proposed manifold,which is employing an integrated reaction chamber/gas-liquid separator (RC-GLS),is characterized by the ability of the successful managing of variable sample volumes (up to 25 ml),in order to achieve high sensitivity.Arsine is able to be selectively generated either from inorganic As(III) or from total arsenic,using different concentrations of HC1 and NaBH_4 solutions.For 8 ml sample volume consumption,the sampling frequency is 40h~(-1).The detection limit is C_L = 0.1 and 0.06 mug I~(-1) for As(III) and total arsenic,respectively.The precision (relative standard deviation) at 2.0 mug 1~(-1) (n = 10) level is s_r = 2.9 and 3.1% for As(III)) and total arsenic,respectively.The performance of the proposed method was evaluated by analyzing the certified reference material NIST CRM 1643d and spiked water samples with various concentration ratios of As(III) to As(V).The method was applied for arsenic speciation in natural waters samples.
机译:开发了一种简单耐用的在线顺序插入系统-氢化物发生原子吸收光谱法(HG-AAS),用于选择性As(III)和总无机砷的测定,无需预先还原步骤。集成的反应室/气液分离器(RC-GLS)的特点是能够成功管理可变样品量(最大25 ml)以实现高灵敏度的能力。无机砷(III)或总砷,使用不同浓度的HC1和NaBH_4溶液。对于8毫升样品量的消耗,采样频率为40h〜(-1)。检测限为C_L = 0.1和0.06杯I〜( -1)对于砷(III)和总砷分别为2.0杯1〜(-1)(n = 10)时的精密度(相对标准偏差)为s_r = 2.9和对于砷(III)为3.1%)和通过分析评估了所提出方法的性能经认证的参考材料NIST CRM 1643d和各种砷(III)与砷(V)浓度比的加标水样品。该方法用于天然水样品中的砷形态分析。

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