首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >TOTAL MERCURY DETERMINATION IN BIOLOGICAL AND ENVIRONMENTAL STANDARD SAMPLES BY GOLD AMALGAMATION FOLLOWED BY COLD VAPOR ATOMIC ABSORPTION SPECTROMETRY
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TOTAL MERCURY DETERMINATION IN BIOLOGICAL AND ENVIRONMENTAL STANDARD SAMPLES BY GOLD AMALGAMATION FOLLOWED BY COLD VAPOR ATOMIC ABSORPTION SPECTROMETRY

机译:气相色谱-原子吸收光谱法测定金和样品中的汞总量-测定生物和环境标准样品。

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As a result of industrialization and changes in the environment during the twentieth century, human and animals are exposed to numerous chemical forms of mercury, including elemental mercury vapor (Hg-0), inorganic mercurous (Hg+) and mercuric (Hg2+) compounds, and organic mercuric (R-Hg+ or R-Hg-R, where R represents any organic ligand) compounds. All forms of mercury have toxic effects, therefore, it is important to determine total mercury in biological and environmental samples to establish baseline levels. This paper highlights the methodology developed for total mercury determination in biological and environmental samples using preconcentration by mercury amalgamation accessory followed by cold vapor atomic absorption spectrometry. The high-pressure microwave digested mercury samples were chemically reduced by stannous chloride and the vapor generated was collected on a mercury amalgamation tube (MAT). The concentrated mercury was revolatilized by rapid heating of the MAT to 500-800 degrees C and was transferred to the absorption cell for determination by cold vapor atomic absorption spectrometry. The preconcentration on the MAT and subsequent revolatilization methodology was compared with the cold vapor atomic absorption determination without the preconcentration step. The preconcentration proved to be sensitive and as the result of the high sensitivity, small sample volumes were analyzed and only short sampling rimes were required. The values for NIST certified human urine, apple leaves, rice flour, bovine liver, buffalo sediments, estuarine sediments, and coal fly ash standard samples were found to be 0.103, 0.067, 0.013, 0.006, 1.267, 0.013, and 0.233 ppm, respectively, versus the certified values of 0.105, 0.044, 0.0058, 0.004, 1.440, 0.063, and 0.16 ppm, respectively. The method is thus suitable for continuous monitoring of mercury and for the fast and reliable determination of mercury in biological and environmental samples, even at background levels. (C) 1996 Academic Press, Inc. [References: 24]
机译:由于20世纪的工业化和环境变化,人类和动物暴露于多种化学形式的汞中,包括元素汞蒸气(Hg-0),无机汞(Hg +)和汞(Hg2 +)化合物,以及有机汞(R-Hg +或R-Hg-R,其中R代表任何有机配体)化合物。所有形式的汞均具有毒性作用,因此,重要的是确定生物和环境样品中的总汞以建立基线水平。本文重点介绍了通过汞齐混物预浓缩,然后进行冷蒸气原子吸收光谱法测定生物和环境样品中的总汞而开发的方法。高压微波消解的汞样品被氯化亚锡化学还原,产生的蒸汽收集在汞齐管(MAT)中。通过将MAT快速加热到500-800摄氏度,可将浓缩的汞重新挥发,并转移到吸收池中,通过冷蒸气原子吸收光谱法进行测定。将不进行预浓缩步骤的MAT预浓缩和随后的挥发方法与冷蒸气原子吸收测定进行了比较。预浓缩证明是灵敏的,并且由于高灵敏度的结果,分析了小样品量,只需要短的采样边缘。经NIST认证的人尿,苹果叶,米粉,牛肝,水牛沉积物,河口沉积物和粉煤灰标准样品的值分别为0.103、0.067、0.013、0.006、1.267、0.013和0.233 ppm ,而认证值分别为0.105、0.044、0.0058、0.004、1.440、0.063和0.16 ppm。因此,该方法适用于连续监测汞以及即使在背景水平下也能快速可靠地测定生物和环境样品中的汞。 (C)1996 Academic Press,Inc. [参考:24]

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