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首页> 外文期刊>Journal of Analytical Atomic Spectrometry >Speciation of inorganic As and Sb in natural waters by total reflection X-ray fluorescence following selective hydride generation and trapping onto quartz reflectors coated with nanostructured Pd
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Speciation of inorganic As and Sb in natural waters by total reflection X-ray fluorescence following selective hydride generation and trapping onto quartz reflectors coated with nanostructured Pd

机译:选择性氢化物生成后,通过全反射X射线荧光并捕获到涂有纳米结构钯的石英反射器上,自然水中无机砷和锑的形态

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In this work, a novel analytical approach for the speciation of inorganic As (iAs) and inorganic Sb (iSb) by total reflection X-ray fluorescence based on the selective generation of arsine and stibine followed by trapping onto quartz reflectors containing immobilized palladium nanoparticles (Pd NPs) is developed. Pd NPs were synthesized by chemical reduction under mild conditions (i.e., a water:ethanol mixture was used as the reducing agent) and immobilized onto quartz substrates following the silanization strategy with 3-mercaptopropyltrimethoxysilane. For microextraction and preconcentration of iAs and iSb, volatile hydrides generated in a continuous flow system were flushed onto the immobilized Pd NPs for catalytic decomposition at ambient temperature. A 26-2III factorial fractional design was used for screening the effect of the variables involved in the hydride generation and preconcentration steps. Selective trapping of As(iii) and Sb(iii) was accomplished following arsine and stibine generation under different reaction conditions, i.e., selective determination of As(iii) in citric acid/citrate buffer medium (pH 4.5) and selective determination of Sb(iii) in a highly acidic medium (pH < 2). In addition, As(v) and Sb(v) were pre-reduced to As(iii) and Sb(iii) with a KI-ascorbic acid mixture for simultaneous determination of total iAs and total iSb. The As(v) and Sb(v) contents were estimated by the difference between both measurements. Limits of detection (LODs) of 0.09, 0.10, 0.50 and 0.80 μg L~(-1) for As(iii), As(v), Sb(iii) and Sb(v) were obtained, respectively. Overall efficiencies of 75% for iAs and 80% for iSb were obtained. Speciation analysis of iAs and iSb in natural waters at the sub-ppb level is demonstrated.
机译:在这项工作中,一种基于选择性生成approach和锑的全反射X射线荧光分析无机砷(iAs)和无机锑(iSb)的形态的新颖分析方法,然后捕获到包含固定化钯纳米粒子的石英反射器上(开发了Pd NPs。通过在温和的条件下化学还原来合成Pd NPs(即使用水:乙醇混合物作为还原剂),并按照3-巯基丙基三甲氧基硅烷的硅烷化策略将其固定在石英基板上。为了进行iAs和iSb的微萃取和预浓缩,将连续流系统中生成的挥发性氢化物冲洗到固定的Pd NP上,以在环境温度下催化分解。 26-2III阶乘分数设计用于筛选参与氢化物生成和预浓缩步骤的变量的影响。在不同反应条件下生成a和锑后,选择性捕集As(iii)和Sb(iii),即在柠檬酸/柠檬酸盐缓冲液(pH 4.5)中选择性测定As(iii),并选择性测定Sb(iii)。 iii)在高酸性介质(pH <2)中。此外,用KI-抗坏血酸混合物将As(v)和Sb(v)预还原为As(iii)和Sb(iii),以便同时测定总iAs和总iSb。通过两次测量之间的差异估算As(v)和Sb(v)的含量。 As(iii),As(v),Sb(iii)和Sb(v)的检出限(LOD)分别为0.09、0.10、0.50和0.80μgL〜(-1)。对于iAs和iSb,总效率分别为75%和80%。演示了亚ppb级天然水中iAs和iSb的形态分析。

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  • 来源
    《Journal of Analytical Atomic Spectrometry》 |2017年第9期|1705-1712|共8页
  • 作者单位

    Departamento de Química Analítica y Alimentaria, Área de Química Analítica, Facultad de Química, Universidad de Vigo, Campus As Lagoas-Marcosende S, Vigo, Spain;

    Departamento de Química Analítica y Alimentaria, Área de Química Analítica, Facultad de Química, Universidad de Vigo, Campus As Lagoas-Marcosende S, Vigo, Spain;

    Departamento de Química Analítica y Alimentaria, Área de Química Analítica, Facultad de Química, Universidad de Vigo, Campus As Lagoas-Marcosende S, Vigo, Spain;

    Departamento de Química Analítica y Alimentaria, Área de Química Analítica, Facultad de Química, Universidad de Vigo, Campus As Lagoas-Marcosende S, Vigo, Spain;

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