摘要
利用四丁基溴化铵(TBAB)-硫酸铵-水双水相体系,研究了铁-邻二氮菲[Fe(phen)3]络合物在二相中的萃取行为。Fe4+与邻二氮菲形成稳定的1:3的配合物后,被萃取到四丁基溴化铵相中,与邻二氮菲法相比,在511 nm处摩尔吸光系数中增加了10倍(由1.1×104L/(mol·cm)增加到1.1×105L/(mol·cm)),可有效提高邻二氮菲法的检出限。方法的线性回归方程A=0.0041+0.0075ρ,相关系数R=0.9993,线性范围0~50μg/25 m L。
An aqueous two-phase system of tetrabutylammonium bromide( TBAB)-( NH4)2SO4mixture has been developed for the determination of the Fe2 +ion chelated with 1,10-Phenanthroline monohydrate( phen)and formed Fe( phen)3which could be extracted into TBAB phase( upper phase). Compared with conventional1,10-phenanthroline spectrophotometric method,molar absorption coefficient increased ten times from 1. 1 × 104 to 1. 1 × 105 L /( mol · cm) at λmax511 nm,which would largely improve the detection limit of the ion. The method is robust and accurate. Linear regression equation was A = 0. 0041 + 0. 0075ρ with linear correlation coeffficient R = 0. 9993,and Beer's law was obeyed in the range of 0 ~ 50 μg /25 m L.
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