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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >A sensitive method for the determination of ultra trace levels of reactive bromine species in water using LC-MS/MS
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A sensitive method for the determination of ultra trace levels of reactive bromine species in water using LC-MS/MS

机译:使用LC-MS / MS测定水中反应性溴物质的超痕量水平的敏感方法

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The purpose of this study was to develop and validate a sensitive method for the determination of ultra trace levels of reactive bromine species (RBS) in water. To derivatized RBS, water samples were transferred into vials pre-fortified with an appropriate dose of derivative reagent 3,5-dimethyl-1H-pyrazole (DMPZ). RBS in water samples could be rapidly and stoichiometrically (1:1) derivatized to 4-bromo-3,5-dimethyl-1H-pyrazole, which was directly analyzed on an ultra performance liquid chromatography coupled with triple quadrupole tandem mass spectrometry. Parameters influencing the derivatization efficiency including reaction time, temperature, DMPZ dose, and pH were optimized to be: a molar concentration ratio of DMPZ to RBS a 100:1, pH 5-10, and reaction for 10 min at room temperature. In addition, near 100% of RBS was recovered when using water with salinity of 0-55 as the spiking matrices, suggesting that salinity had negligible effect on the derivatization efficiency. Under the optimized conditions, interday and intraday analyses showed that the recoveries of RBS ranged from 88.0% to 109.8% for samples spiked with 18.0-540 pmol L-1 of RBS, with relative standard deviations less than 3.7%. The method limit of detection and limit of quantification for RBS were 5.8 pmol L-1 and 18.0 pmol L-1, respectively. Compared with currently available methods, our method greatly improved the analytical sensitivity by lowering the limit of detection for more than 100 times. The developed method displayed high reliability and reproducibility in the analysis of ultra trace levels of RBS in seawater and other real fresh water samples.
机译:本研究的目的是开发和验证敏感方法,用于测定水中的超痕量水平(RB)。为了衍生的RBS,将水样品转移到预防剂量的适当剂量的衍生物试剂3,5-二甲基-1H-吡唑(DMPZ)中预制的小瓶中。水样中的RBS可以迅速且化学计量(1:1)衍生至4-溴-3,5-二甲基-1H-吡唑,其在与三重四极杆串联质谱法偶联的超高效液相色谱上直接分析。影响包括反应时间,温度,DMPZ剂量和pH的衍生化效率的参数优化为:DMPZ至RBS 100:1,pH 5-10的摩尔浓度比,并在室温下反应10分钟。此外,在使用0-55的盐度作为尖峰基质时,回收近100%的RBS,表明盐度对衍生效率的影响可忽略不计。在优化的条件下,中间和盘中分析表明,RB的回收率范围为88.0%至109.8%,用于掺入18.0-540pmol L-1的RBS,相对标准偏差小于3.7%。 RBS的检测方法和定量限制分别为5.8pmol L-1和18.0pmol L-1。与目前可用的方法相比,我们的方法通过降低检测限超过100倍,大大提高了分析灵敏度。开发方法显示出海水和其他真正淡水样品中超痕量RBS分析的高可靠性和再现性。

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