Determination of isocyanates by capillary electrophoresis with tris(2,2′-bipyridine) ruthenium(II) electrochemiluminescence

被引:18
作者
Li, Haijuan [1 ,2 ]
Shi, Lihong [1 ,2 ]
Liu, Xiaoqing [1 ,2 ]
Niu, Wenxin [1 ,2 ]
Xu, Guobao [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Peoples R China
[2] Chinese Acad Sci, Grad Univ, Changchun 130022, Peoples R China
基金
中国国家自然科学基金;
关键词
Capillary electrophoresis; Electrochemiluminescence; Electrochemistry; Isocyanates; Ruthenium; SOLID-STATE ELECTROCHEMILUMINESCENCE; ELECTROGENERATED CHEMI-LUMINESCENCE; PERFORMANCE LIQUID-CHROMATOGRAPHY; COMPOSITE FILMS; TERTIARY-AMINES; HEXAMETHYLENE DIISOCYANATE; AIRBORNE ISOCYANATES; ZONE-ELECTROPHORESIS; AQUEOUS-SOLUTION; ULTRATHIN FILMS;
D O I
10.1002/elps.200900281
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
CE with tris(2,2'-bipyridyl) ruthenium(II) (Ru(bpy)(3)(2+)) electrochemiluminescence (ECL) detection for the quantitative determination of isocyanates was first reported. Hexamethylene diisocyanate (HDI) and hexyl isocyanate (HI) were used as the model analytes. Commercially available N,N-diethyl-N'-methylethylenediamine was used as the derivatization reagent. It has both a secondary amine group and a tertiary amine group. The secondary amine group can quantitatively react with isocyanate group, and the tertiary amine group can react with Ru(bpy)(3)(2+) to produce strong ECL signal for sensitive detection. The derivatization reaction was almost instantaneous and is much faster than other reported derivative reactions using other derivative reagents. The urea formed was stable. Linear calibration curve was obtained in the range from 0.01 to 10 mu M for HDI, and 0.02 to 20 mu M for hexyl isocyanate (HI). The detection limit is 0.01 mu M for HDI and 0.02 mu M for HI. The method is more sensitive than UV-detection and electrochemical detection. For practical application, recovery higher than 90% for HDI and HI was
引用
收藏
页码:3926 / 3931
页数:6
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