TY - JOUR
T1 - Enhanced Indirect fluorescence detection of p-nitrophenol, 2,4-dinitrophenol and Trinitrophenol by micellar electrokinetic capillary chromatography with in-column optical-fiber LED-induced fluorescence detection
AU - Huo, Feng
AU - Yuan, Hongyan
AU - Yang, Xiupei
AU - Xiao, Dan
AU - Choi, Martin M.F.
N1 - Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.
PY - 2011
Y1 - 2011
N2 - Enhanced indirect fluorescence detection with in-column optical-fiber LED-induced fluorescence (LED-IF) detection has been developed for the simultaneous separation and determination of p-nitrophenol, 2,4-dinitrophenol and trinitrophenol. The instrumental set-up is simple, cost-effective and the detection method is stable. Different experimental parameters have been studied. The optimum conditions were determined as: running buffer (pH 9.1) composed of 10 mM borate, 80 mM sodium dodecylsulfate and 0.18 μM fluorescein (as a background reagent); applied voltage of 15 kV; working temperature of 25.0°C. The limits of detection (S/N = 3) were 11, 18 and 16 μM for p-nitrophenol, 2,4-dinitrophenol and trinitrophenol, respectively. The nitrophenols were completely separated in 13 min and the number of theoretical plates for p-nitrophenol, 2,4-dinitrophenol and trinitrophenol were 8.1 × 10 6 , 6.5 × 10 6 and 8.4 × 10 6 , respectively. The RSDs (n = 6) for the migration time and the peak area were better than 0.85 and 0.91%, respectively. Our proposed method possesses the advantages of rapidness and good separation efficiency.
AB - Enhanced indirect fluorescence detection with in-column optical-fiber LED-induced fluorescence (LED-IF) detection has been developed for the simultaneous separation and determination of p-nitrophenol, 2,4-dinitrophenol and trinitrophenol. The instrumental set-up is simple, cost-effective and the detection method is stable. Different experimental parameters have been studied. The optimum conditions were determined as: running buffer (pH 9.1) composed of 10 mM borate, 80 mM sodium dodecylsulfate and 0.18 μM fluorescein (as a background reagent); applied voltage of 15 kV; working temperature of 25.0°C. The limits of detection (S/N = 3) were 11, 18 and 16 μM for p-nitrophenol, 2,4-dinitrophenol and trinitrophenol, respectively. The nitrophenols were completely separated in 13 min and the number of theoretical plates for p-nitrophenol, 2,4-dinitrophenol and trinitrophenol were 8.1 × 10 6 , 6.5 × 10 6 and 8.4 × 10 6 , respectively. The RSDs (n = 6) for the migration time and the peak area were better than 0.85 and 0.91%, respectively. Our proposed method possesses the advantages of rapidness and good separation efficiency.
UR - http://www.scopus.com/inward/record.url?scp=80053616686&partnerID=8YFLogxK
U2 - 10.2116/analsci.27.879
DO - 10.2116/analsci.27.879
M3 - Journal article
AN - SCOPUS:80053616686
SN - 0910-6340
VL - 27
SP - 879
EP - 884
JO - Analytical Sciences
JF - Analytical Sciences
IS - 9
ER -