摘要
在邻苯二甲酸氢钾 HCl 乙醇 水溶液中,钼(Ⅵ) 水杨基荧光酮体系在滴汞电极上,于-1.10V(vs.SCE)处有一良好的极谱波,其二阶导数峰电流与钼(Ⅵ)在8×10-10~6×10-8mol L范围内有良好的线性关系,检出限为5×10-10mol L。研究了极谱波的性质和电极反应机理。该方法已用于水及生物样品的测定。
In a buffer solution of potassium biphthalate-HCl, the complex of molybdenum-salicyflorone was adsorbed on the surface of dropping mercury electrode and produced a redution peak at -1.10 V(vs.SCE). Under optimum conditions, the linear range of the concentration of Mo(Ⅵ) with the secondary derivative oscillopolaro graphic peak current was 8×10^(-10)~6×10^(-8) mol/L with the detection limit of 5×10^(-10) mol/L. This method was applied to the determination of molybdenum in water and biological samples with satisfactory results. The mechanism of the electrode process was studied.
出处
《分析试验室》
CAS
CSCD
北大核心
2004年第10期5-8,共4页
Chinese Journal of Analysis Laboratory