Soylak Mustafa, Saracoglu Sibel, Divrikli Umit, Elci Latif
Erciyes Universitesi, Fen-Edebiyat Fakultesi, Kimya Bolumu, 38039 Kayseri, Turkey.
Talanta. 2005 Jun 15;66(5):1098-102. doi: 10.1016/j.talanta.2005.01.030.
Trace amounts of copper, manganese, cobalt, chromium, iron and lead were quantitatively coprecipitated with erbium hydroxide on 0.05M NaOH medium. The coprecipitant could be easily dissolved with 1M nitric acid. The presence of up to 15g/l of erbium ions did not interfere with the atomic absorption spectrometric determination of analyte ions. The recovery values for analyte ions were higher than 95%. The concentration factor was 25-fold. Coprecipitation parameters including reagent amounts and matrix effects are discussed. The relative standard deviations of the determinations were below 9%. The time required for the coprecipitation was about 30min. The proposed method was successfully applied for the determination of trace amounts of analyte ions in urine, soil and sediment, natural water samples.
在0.05M氢氧化钠介质中,痕量的铜、锰、钴、铬、铁和铅与氢氧化铒定量共沉淀。共沉淀剂可用1M硝酸轻松溶解。高达15g/l的铒离子的存在不干扰分析物离子的原子吸收光谱测定。分析物离子的回收率高于95%。浓缩因子为25倍。讨论了包括试剂量和基体效应在内的共沉淀参数。测定的相对标准偏差低于9%。共沉淀所需时间约为30分钟。所提出的方法成功应用于尿液、土壤、沉积物、天然水样中痕量分析物离子的测定。