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Flow injection-chemical vapor generation atomic fluorescence spectrometry hyphenated system for organic mercury determination: A step forward

机译:流动注射化学蒸气发生原子荧光光谱联用系统测定有机汞:向前迈进了一步

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Monomethylmercury and ethylmercury were determined on line using flow injection-chemical vapor generation atomic fluorescence spectrometry without neither requiring a pre-treatment with chemical oxidants, nor UV/MW additional post column interface, nor organic solvents, nor complexing agents, such as cysteine. Inorganic mercury, monomethylmercury and ethylmercury were detected by atomic fluorescence spectrometry in an Ar/H2 miniaturized flame after sodium borohydride reduction to Hg°, monomethylmercury hydride and ethylmercury hydride, respectively. The effect of mercury complexing agent such as cysteine, ethylendiaminotetracetic acid and HC1 with respect to water and Ar/H2 microflame was investigated. The behavior of inorganic mercury, monomethylmercury and ethylmercury and their cysteine-complexes was also studied by continuous flow-chemical vapor generation atomic fluorescence spectrometry in order to characterize the reduction reaction with tetrahydroborate. When complexed with cysteine, inorganic mercury, monomethylmercury and ethylmercury cannot be separately quantified varying tetrahydroborate concentration due to a lack of selectivity, and their speciation requires a pre-separation stage (e.g. a chromatographic separation). If not complexed with cysteine, monomethylmercury and ethylmercury cannot be separated, as well, but their sum can be quantified separately with respect to inorganic mercury choosing a suitable concentration of tetrahydroborate (e.g. 10~(-5) mol L~(-1)), thus allowing the organic/inorganic mercury speciation. The detection limits of the flow injection-chemical vapor generation atomic fluorescence spectrometry method were about 45 nmol L~(-1) (as mercury) for all the species considered, a relative standard deviation ranging between 1.8 and 2.9% and a linear dynamic range between 0.1 and 5 μmol L~(-1) were obtained. Recoveries of monomethylmercury and ethylmercury with respect to inorganic mercury were never less than 91%. Flow injection-chemical vapor generation atomic fluorescence spectrometry method was validated by analyzing the TORT-1 certificate reference material, which contains only monomethylmercury, and obtaining 83 ± 5% of monomethylmercury recovered, respectively. This method was also applied to the determination of monomethylmercury in saliva samples.
机译:使用流动注射-化学蒸气发生原子荧光光谱法在线测定一甲基汞和乙基汞,不需要用化学氧化剂进行预处理,也不需要在柱后界面处添加UV / MW,也不需要有机溶剂,也不需要络合剂,例如半胱氨酸。硼氢化钠还原为Hg°后,在Ar / H2小型火焰中通过原子荧光光谱法分别检测无机汞,一甲基汞和乙基汞,一甲基氢化物和乙基汞氢化物。研究了汞络合剂(例如半胱氨酸,乙基苯二氨基四乙酸和HCl)对水和Ar / H2微火焰的影响。还通过连续流化学气相生成原子荧光光谱法研究了无机汞,一甲基汞和乙基汞及其半胱氨酸络合物的行为,以表征四氢硼酸盐的还原反应。当与半胱氨酸络合时,由于缺乏选择性,无法分别定量改变四氢硼酸根浓度的无机汞,一甲基汞和乙基汞,它们的形成需要一个预分离阶段(例如色谱分离)。如果不与半胱氨酸络合,也不能分离出单甲基汞和乙基汞,但是它们的总和可以根据无机汞分别定量,选择合适的四氢硼酸盐浓度(例如10〜(-5)mol L〜(-1))。 ,因此可以形成有机/无机汞形态。流动注射-化学气相产生原子荧光光谱法的检测限为所考虑的所有物种均为约45 nmol L〜(-1)(以汞计),相对标准偏差为1.8%至2.9%,线性动态范围得到0.1-5μmolL〜(-1)。相对于无机汞,一甲基汞和乙基汞的回收率不低于91%。通过分析仅含有单甲基汞的TORT-1证书参考材料,并分别回收了83±5%的回收的单甲基汞,从而验证了流动注射化学气相生成原子荧光光谱法的有效性。该方法还用于唾液样品中单甲基汞的测定。

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