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Total nitrogen determination by flow injection using on-line microwave-assisted digestion

机译:在线微波辅助消解通过流动注射测定总氮

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A method for the determination of total nitrogen in wastewaters involving flow injection and on-line microwave-assisted digestion is described. The method is based on the oxidation of nitrogen-containing compounds to nitrate by means of peroxodisulfate using a microwave oven as a radiation source. Nitrate is determined by the Griess-Ilosvay reaction, after reduction to nitrite by hydrazine under alkaline conditions, using sulfanilamide and N-(1-naphthyl)ethylene diamine. A thorough study of the factors affecting the digestion process has been carried out using several nitrogen-containing compounds as test substances. Under the optimized conditions, the described method allows quantitative digestion of all the model compounds for concentrations up to 20 mg l(-1) N. The method enables the analysis of 10 samples in triplicate per hour, the relative standard deviation (RSD) of 10 replicates being ca. 3%. The detection limit (3xSD of blank) is 0.21 mg l(-1) N. The system has been applied to the determination of total nitrogen in wastewaters and the results have been compared with those obtained by Kjeldahl digestion. (C) 1997 Elsevier Science B.V.
机译:描述了一种测定废水中总氮的方法,包括流动注射和在线微波辅助消解。该方法基于使用微波炉作为辐射源通过过二硫酸盐将含氮化合物氧化为硝酸盐。在碱性条件下,使用磺酰胺和N-(1-萘基)乙二胺通过肼还原为亚硝酸盐后,通过Griess-Ilosvay反应确定硝酸盐。使用几种含氮化合物作为测试物质已经对影响消化过程的因素进行了深入研究。在优化的条件下,所描述的方法允许定量分析所有模型化合物的最大浓度为20 mg l(-1)N。该方法能够每小时分析10个样品,一式三份,相对标准偏差(RSD)为大约重复10次。 3%。检出限(空白的3xSD)为0.21 mg l(-1)N。该系统已用于测定废水中的总氮,并将结果与​​凯氏定氮法得到的结果进行了比较。 (C)1997年Elsevier Science B.V.

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