Department of Chemistry, Faculty of Basic Sciences, University of Mohaghegh Ardabili, Ardabil, Iran.
Anal Chim Acta. 2011 Oct 17;704(1-2):146-53. doi: 10.1016/j.aca.2011.07.005. Epub 2011 Jul 26.
A new method was proposed for the determination of ammonium based on the preconcentration with dodecylbenzene sulfonate modified magnetite nanoparticles. Ammonium was oxidized to nitrite by hypobromite and then the nitrite produced was determined spectrophotometrically, using sulfabenzamide and N-(1-naphthyl) ethylenediamine after solid phase extraction. The azo dye produced was desorbed by an appropriate small volume of sodium hydroxide prior to the absorbance measurement. The linear calibration graphs were obtained in the concentration range of 0.03-6.00 ng mL(-1) ammonium. The relative standard deviation and recovery percents were 1.0 and 99.0, respectively, for 1.0 ng mL(-1) ammonium, and the limit of detection was 3.2 ng L(-1) ammonium. The interfering effects of a large number of diverse ions on the determination of ammonium were studied. The method was applied to the determination of ammonium in various types of water resources. The results revealed a high efficiency for the recommended ammonium determination method.
提出了一种基于十二烷基苯磺酸钠修饰的磁铁矿纳米粒子预富集测定铵的新方法。在过溴酸钠存在下,铵被氧化为亚硝酸盐,然后通过固相萃取后使用磺酰胺和 N-(1-萘基)乙二胺进行分光光度法测定。在进行吸光度测量之前,用适量的小体积氢氧化钠将生成的偶氮染料解吸。在 0.03-6.00ng mL(-1) 铵浓度范围内获得了线性校准曲线。对于 1.0ng mL(-1) 铵,相对标准偏差和回收率分别为 1.0 和 99.0,检测限为 3.2ng L(-1) 铵。研究了大量不同离子对铵测定的干扰影响。该方法应用于各种类型水资源中铵的测定。结果表明,所推荐的铵测定方法效率很高。