Simultaneous Determination of Ethyleneamines by Reversed-Phase Ion-Pair Chromatography with Ultraviolet Detection Using on-Line Complexation with Copper(II) Ion

被引:1
|
作者
Yudo, Azusa [1 ,2 ]
Kemmei, Tomoko [1 ,2 ]
Kodama, Shuji [3 ]
Inoue, Yoshinori [2 ,4 ]
Kagaya, Shigehiro [2 ]
机构
[1] Toyama Inst Hlth, 17-1 Nakataikoyama, Imizu 9390363, Japan
[2] Univ Toyama, Fac Engn, Dept Environm Appl Chem, 3190 Gofuku, Toyama 9308555, Japan
[3] Tokai Univ, Sch Sci, Dept Chem, 4-1-1 Kitakaname, Hiratsuka 2591292, Japan
[4] Aichi Inst Technol, Fac Engn, Dept Appl Chem, 1247 Yachigusa,Yakusa-cho, Toyota 4700392, Japan
基金
日本学术振兴会;
关键词
Ethyleneamines; Reversed-phase ion-pair liquid chromatography; Cu(II) ion; Ultraviolet detection; PERFORMANCE LIQUID-CHROMATOGRAPHY; CONTACT-DERMATITIS; TRIETHYLENETETRAMINE; FLUORESCENCE; ACIDS; METABOLITES; POLYAMINES; SEPARATION; HARDENERS; ALCOHOLS;
D O I
10.1007/s10337-024-04342-y
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A selective and simple method was developed for the determination of four ethyleneamines (EAs), i.e., ethylenediamine (EDA), diethylenetriamine (DETA), triethylenetetramine (TETA), and tetraethylenepentamine (TEPA), by reversed-phase ion-pair chromatography with ultraviolet detection. The method is based on the on-line complexation of EAs with a Cu(II) ion added to the mobile phase. The Cu(II) complexes with EAs (Cu(II)-EA complexes) were well separated on a reversed-phased column, using 1-octanesulfonate as an ion-pairing reagent. The concentrations of 1-octanesulfonate and acetonitrile in the mobile phase significantly influenced the retention times of EAs. The high concentration of the Cu(II) ion in the mobile phase resulted in the increase of the baseline noise. A mixture of acetonitrile and 50 mM acetate buffer at pH 5.5 (23:77, v/v) which contains 0.5 mM CuSO4 and 20 mM 1-octanesulfonic acid sodium salt was used as the mobile phase. Cu(II)-EA complexes could be detected at 243 nm. The limits of quantification of EAs (S/N = 10) were 0.003 mM for EDA, DETA, and TETA and 0.01 mM for TEPA. The calibration curves were linear over three orders of magnitude of EA concentrations with high correlation coefficients (r2 = 1.000). The proposed method was successfully applied to determine EAs in epoxy resin curing agents.
引用
收藏
页码:463 / 470
页数:8
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