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Determination of the Total Inorganic and Ammoniacal Nitrogens in Water by Gas-Phase Molecular-Absorption Spectrometry

机译:气相分子吸收光谱法测定水中的总无机氮和氨氮

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Based on a vapor-liquid equiribrium of ammonia, a simplified and rapid technique was developed for the determination of the total inorganic and ammoniacal nitrogens in aqueous solution. Ammonium ion was converted into gaseous ammonia by adding a sodium hydroxide solution to a sample solution. The generated ammonia was directly introduced into a quartz cell in order to measure the molecular absorption. As for the determination of the total inorganic nitrogen, the sample solution was pretreated with titanium(III) chloride solution in order to reduce nitrate and nitrite ions to ammonium ion. The ammonia was then evolved and determined in the same manner as mentioned above. The detection limit (3S/N) of 0.01μg cm-3 for both ammonia and the total inorganic nitrogen was obtained. The calibrationgraph was linear up to 0.8μgN cm-3 for each nitrogen species. The relative standard deviations for five replicate measurements were 3.9, 4.5 and 4.7% for 0.40μg cm-3 of nitrogen present in the form of ammonium, nitrate and nitrite ions, respectively. The analytical results for some environmental and industrial water samples are presented.
机译:基于氨的气液平衡,开发了一种简便快速的技术来测定水溶液中的无机和氨氮总量。通过将氢氧化钠溶液添加到样品溶液中,铵离子转化为气态氨。将产生的氨直接引入石英池中以测量分子吸收。关于总无机氮的测定,将样品溶液用氯化钛(III)预处理,以将硝酸根和亚硝酸根离子还原为铵离子。然后以与上述相同的方式释放并确定氨。氨和总无机氮的检出限(3S / N)为0.01μgcm-3。每种氮素的校准图线性最高为0.8μgNcm-3。对于以铵离子,硝酸根离子和亚硝酸根离子形式存在的0.40μgcm-3的氮,五次重复测量的相对标准偏差分别为3.9%,4.5%和4.7%。给出了一些环境和工业用水样品的分析结果。

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