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使用多通道化学蒸气发生原子荧光光谱仪同时测定沿海海水中痕量汞、砷、锑和铋

Simultaneous Measurement of Trace Levels of Hg, As, Sb, and Bi in Coastal Seawater with a Multichannel Chemical Vapor Generation Atomic Fluorescence Spectrometer.

作者信息

Chen Luodan, Lin Qinling, Yuan Dongxing, Gong Zhenbin

机构信息

State Key Laboratory of Marine Environmental Science, Xiamen University, Xiamen 361102, PR China.

Center for Marine Environmental Chemistry and Toxicology, College of the Environment & Ecology, Xiamen University, Xiamen 361102, PR China.

出版信息

Anal Chem. 2023 Oct 24;95(42):15621-15627. doi: 10.1021/acs.analchem.3c02755. Epub 2023 Oct 10.

DOI:10.1021/acs.analchem.3c02755
PMID:37816153
Abstract

Trace levels of Hg, As, Sb, and Bi in coastal seawater have been simultaneously detected by a laboratory-built multichannel chemical vapor generation coupled to an atomic fluorescence spectrometer. The system was configured with a built-in electrochemical H generator as the fuel supplier to replace chemical H produced by the oxidation of potassium borohydride under acidic conditions in traditional instruments. The electrochemical H generator not only isolated the atomization process from the chemical vapor injection process but also improved the stability of atomization, excitation, and fluorescence emission in the hydrogen flame, making it easier to optimize conditions for CVG while introducing evaporating multielement vapors. Calibrations were obtained using a mixed standard solution of Hg(II), As(III), Sb(III), and Bi(III). The addition of KBr to a 3% (/) HCl solution was selected as the preservative to ensure the stability of 0.10 μg/L Hg(II) in a multielement standard solution for at least 15 days while also preserving μg/L levels of As(III), Sb(III), and Bi(III) stable. The method detection limits (LOD, 3σ) were 0.001, 0.015, 0.010, and 0.005 μg/L for Hg, As, Sb, and Bi, respectively. The relative standard deviations (RSD, = 7) of the standard spiked seawater samples were 3.2% (0.020 μg/L Hg), 1.2% (0.50 μg/L As), 1.0% (0.50 μg/L Sb), and 3.5% (0.050 μg/L Bi), respectively. The recoveries of seawater samples spiked with different salinities were in the range of 84.5%(Sb)-114%(Hg). The system has been successfully applied to the simultaneous analysis of the four elements in the seawater samples collected from Xiamen Bay, Southeast China.

摘要

利用实验室构建的多通道化学蒸气发生装置与原子荧光光谱仪联用,同时检测了沿海海水中痕量的汞、砷、锑和铋。该系统配置了内置的电化学氢发生器作为燃料供应源,以替代传统仪器中硼氢化钾在酸性条件下氧化产生的化学氢。电化学氢发生器不仅将雾化过程与化学蒸气注入过程隔离开来,还提高了氢火焰中雾化、激发和荧光发射的稳定性,使得在引入蒸发多元素蒸气时更容易优化化学蒸气发生条件。使用汞(II)、砷(III)、锑(III)和铋(III)的混合标准溶液进行校准。选择向3%(/)盐酸溶液中添加溴化钾作为防腐剂,以确保多元素标准溶液中0.10 μg/L汞(II)的稳定性至少为15天,同时也能保持μg/L水平的砷(III)、锑(III)和铋(III)稳定。汞、砷、锑和铋的方法检测限(LOD,3σ)分别为0.001、0.015、0.010和0.005 μg/L。加标海水样品的相对标准偏差(RSD, = 7)分别为3.2%(0.020 μg/L汞)、1.2%(0.50 μg/L砷)、1.0%(0.50 μg/L锑)和3.5%(0.050 μg/L铋)。不同盐度加标海水样品的回收率在84.5%(锑) - 114%(汞)范围内。该系统已成功应用于对中国东南部厦门湾采集的海水样品中这四种元素的同时分析。

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