摘要
在 0 .0 5mol/L氯乙酸 氯乙酸钠 (pH 3.0 )介质中 ,Pb2 + 与二溴邻苯二胺双草酰胺酸酯 (DBAC)生成络合物 ,并吸附于电极表面 ,于 - 0 .6 0V(vs.SCE)得到络合物吸附还原波。其二次微分极谱峰电流与Pb2 + 浓度在 2 .5× 10 -8~ 6 .0× 10 -6mol/L内呈良好的线性关系 ;检出限为 1.5× 10 -8mol/L。方法应用于陶瓷颜料、矿石、人发中微量铅的测定 ,结果满意。
In a buffer solution of 0.05 mol/L ClCH 2COOH-ClCH 2COONa(pH 3.0), the complex of lead-dibrom-o-benzenediamine-diacetamide ester (DBAC) was adsorbed on the surface of mercury electrode and produced a reduction peak at -0.60 V(vs. SCE).The detection limit and the linear range of the concentration of Pb to the single-sweep 2nd-order derivative osilloplarographic peak current (I ″ p) were 1.5×10 -8 mol/L and 2.5×10 -8~6 0×10 -6 mol/L Pb, respectively.The method has been applied to the determination of trace Pb in hair, dyestuff and ore samples with satisfactory results. The mechanism of the electrode process has also been studied.
出处
《分析化学》
SCIE
EI
CAS
CSCD
北大核心
2004年第1期67-70,共4页
Chinese Journal of Analytical Chemistry