摘要
Pb2+、Cd2+、Hg2+在pH6.5的硼砂-盐酸缓冲溶液中,与四(4-三甲铵基苯基)卟啉(TAPP)生成稳定配合物,采用KI和低聚度聚乙烯醇(PVA)增敏、增溶,Pb2+、Cd2+、Hg2+的εmax分别为ε481.5(4.9×105L·mol-1·cm-1)、ε457(7.9×105L·mol-1·cm-1)、ε444.5(8.1×104L·mol-1·cm-1)。在三吸收峰相互重叠的情形下,利用比波谱导数和零交点法,同时测定它们的含量,Pb2+、Cd2+、Hg2+的检出限分别达4μg/L、2μg/L和10μg/L。方法计算简便、快速。
In the buffer intensity of the borax and hydrochloric acid with pH6.5 , Pb 2+ 、Cd 2+ and Hg 2+ react with Tetra 4 trimethylaminobenzene porphyrin [T(4 TMAP)P] to produce a stable complex , then Pb 2+ 、Cd 2+ and Hg 2+ 's ε max can be found respectively to be ε 481.5 (4.9×10 5 L·mol -1 ·cm -1 )、 ε 457 (7.9×10 5 L·mol -1 ·cm -1 )and ε 444.5 (8.1×10 4 L·mol -1 ·cm -1 ), after the adoption of spike and solubilization by means of KI and low degree of PVA(polyvinyl alcohol). Under the overlapping condition of 3 absorption peaks , their contents can be determined by means of derivative ratio spectrum and zero crossing. They detection limit is 4μg /L, 2μg /L and 10μg/L respectively and the calculating method is simple and rapid.
出处
《光谱实验室》
CAS
CSCD
1999年第1期37-41,共5页
Chinese Journal of Spectroscopy Laboratory
关键词
比波谱导数
零交点
配合物
铅
镉
汞
测定
TAPP
Derivative Ratio Spectrum, Zero Crossing,Tetra 4 trimethylaminobenzene Porphyrin, Complex.