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首页> 外文期刊>Analytica chimica acta >Ultra-trace determination of bromate in drinking waters by means of microbore column ion chromatography and on-line coupling with inductively coupled plasma mass spectrometry
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Ultra-trace determination of bromate in drinking waters by means of microbore column ion chromatography and on-line coupling with inductively coupled plasma mass spectrometry

机译:微孔柱离子色谱-电感耦合等离子体质谱在线耦合超痕量测定饮用水中的溴酸盐

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A method for ultra-trace determination of bromate in drinking waters using on-line coupling of ion chromatography (IC) and inductively coupled plasma mass spectrometry (ICP-MS) has been developed. The method utilizes the microbore column technique in combination with a self-made high-capacity and high-performance anion-exchanger. The high capacity of the separation column as well as an optimized elution system based on NH4NO3 allows a direct analysis of almost every water sample without matrix elimination. Even more, the use of large injection volumes is possible. No trace enrichment is required because of the sensitivity of ICP-MS detection. The effort on sample pretreatment is therefore reduced to zero. The method detection limits for bromate in the drinking and mineral waters investigated are in the 50-65 ng/l range, corresponding to absolute detection limits of 44-58 pg. Retention behaviour of bromate as well as signal-to-noise (SNR) and signal-to-background (SBR) ratios are dependent on the sample composition. The within-run imprecision of the presented IC-ICP-MS coupling is 5% at a concentration level of 500 ng/l bromate. The time spent on a complete analysis is 8-15 min, depending on the bromide content of the sample. Considering sensitivity as well as imprecision and short analysis times, the described IC-ICP-MS coupling is well suited for precise routine analysis of bromate in drinking waters at sub-mu g l(-1)-levels. (C) 1998 Elsevier Science B.V. [References: 27]
机译:开发了一种使用离子色谱在线耦合(IC)和电感耦合等离子体质谱法(ICP-MS)超痕量测定饮用水中溴酸盐的方法。该方法利用微孔柱技术结合自制的高容量和高性能阴离子交换剂。分离柱的高容量以及基于NH4NO3的优化洗脱系统可直接分析几乎所有水样,而无需去除基质。甚至可以使用大的进样量。由于ICP-MS检测的灵敏度,因此无需富集痕量。因此,样品预处理的工作量减少到零。在所研究的饮用水和矿泉水中,溴酸盐的方法检出限在50-65 ng / l范围内,对应于44-58 pg的绝对检出限。溴酸盐的保留行为以及信噪比(SNR)和信噪比(SBR)取决于样品成分。在500 ng / l溴酸盐的浓度水平下,所提出的IC-ICP-MS偶联的运行中不精确度为5%。进行完整分析所需的时间为8-15分钟,具体取决于样品中溴化物的含量。考虑到灵敏度以及不精确性和较短的分析时间,所描述的IC-ICP-MS耦合非常适合于精确的常规分析,饮用水中亚微克l(-1)级的溴酸盐。 (C)1998 Elsevier Science B.V. [参考:27]

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