Ping Q, Naixing W, Zhikun S, Jinghe Y, Zhendong L
Shandong Provincial Analysis Test Centre, 250014, Jinan, People's Republic of China.
Anal Bioanal Chem. 1996 Aug;356(2):146-9. doi: 10.1007/s0021663560146.
The absorption spectra of 4f electron transitions of the systems of neodymium and erbium with 2-isobutylformyl-1,3-dione-indane and TX-100 have been studied by normal and derivative spectrophotometry. Their molar absorptivities at the maximum absorption bands are about 7.2 (at 571 nm) times greater for neodymium and 13.1 (at 519 nm) times greater for erbium than those in the absence of the complexing agents. Use of second derivative spectra both eliminates the interference from other rare earths and increases the sensitivity from neodymium and erbium. Beer's law is obeyed from 0 approximately 20 microg/ml for neodymium and 0 approximately 25 microg/ml for erbium. The relative standard deviations are 1.2% and 1.6% for 5.0 microg/ml of neodymium and 8.0 microg/ml of erbium, respectively. The detection limits (signal-to-noise ratio=2) are 0.14 microg/ml and 0.20 microg/ml. A method for the direct determination of neodymium and erbium in rare earth mixtures with good accuracy and selectivity is proposed.
采用常规分光光度法和导数分光光度法研究了钕、铒与2-异丁基甲酰基-1,3-二酮茚满和TX-100体系中4f电子跃迁的吸收光谱。它们在最大吸收带处的摩尔吸光系数,钕比不存在络合剂时约大7.2倍(在571nm处),铒比不存在络合剂时约大13.1倍(在519nm处)。使用二阶导数光谱既消除了其他稀土元素的干扰,又提高了钕和铒的灵敏度。钕在0至约20μg/ml、铒在0至约25μg/ml范围内符合比尔定律。对于5.0μg/ml的钕和8.0μg/ml的铒,相对标准偏差分别为1.2%和1.6%。检测限(信噪比=2)分别为0.14μg/ml和0.20μg/ml。提出了一种直接测定稀土混合物中钕和铒的方法,该方法具有良好的准确性和选择性。