TY - JOUR
T1 - Analysis of aromatic sulfonates in water by solid-phase extraction and capillary electrophoresis
AU - Loos, Robert
AU - Niessner, Reinhard
N1 - Funding Information:
Martin Sörensen is thanked for providing some sulfonates, Matthias Schedl for software troubleshooting and reviewing the manuscript and Michael G. Weller for insightful discussions. The financial support by the BMBF (project 02WT96130) is gratefully acknowledged.
PY - 1998/10/2
Y1 - 1998/10/2
N2 - The separation of 14 different aromatic sulfonates of environmental concern by capillary (zone) electrophoresis (CZE) is presented. A new off-line solid-phase extraction (SPE) enrichment procedure, that is compatible with CE analysis, was developed, using the styrene-divinylbenzene adsorbent LiChrolut EN. The combined method of SPE and CE allows the determination of aromatic sulfonates in water samples in the low μg/l range. Separations are performed with a simple sodium borate buffer at pH 9.3. Analytes are detected by UV absorbance and fluorescence emission with a Xe-lamp excitation source, and both principles are compared. The recoveries for most of the sulfonates are >70% for the extraction from spiked tap and river water. The average method precision is <20% for replicate analyses. Very hydrophilic sulfonates cannot be extracted by this method. The detection limit of the combined method of SPE enrichment and CE analysis is approximately 0.1 μg/l for 200-ml water samples. The performance of the method was checked with the analysis of river and contaminated seepage water. Copyright (C) 1998 Elsevier Science B.V.
AB - The separation of 14 different aromatic sulfonates of environmental concern by capillary (zone) electrophoresis (CZE) is presented. A new off-line solid-phase extraction (SPE) enrichment procedure, that is compatible with CE analysis, was developed, using the styrene-divinylbenzene adsorbent LiChrolut EN. The combined method of SPE and CE allows the determination of aromatic sulfonates in water samples in the low μg/l range. Separations are performed with a simple sodium borate buffer at pH 9.3. Analytes are detected by UV absorbance and fluorescence emission with a Xe-lamp excitation source, and both principles are compared. The recoveries for most of the sulfonates are >70% for the extraction from spiked tap and river water. The average method precision is <20% for replicate analyses. Very hydrophilic sulfonates cannot be extracted by this method. The detection limit of the combined method of SPE enrichment and CE analysis is approximately 0.1 μg/l for 200-ml water samples. The performance of the method was checked with the analysis of river and contaminated seepage water. Copyright (C) 1998 Elsevier Science B.V.
KW - Aromatic sulfonates
KW - Seepage water
KW - Solid-phase extraction
KW - Sulfonates, aromatic
KW - Water analysis
UR - http://www.scopus.com/inward/record.url?scp=0031691321&partnerID=8YFLogxK
U2 - 10.1016/S0021-9673(98)00620-7
DO - 10.1016/S0021-9673(98)00620-7
M3 - Article
C2 - 9809447
AN - SCOPUS:0031691321
SN - 0021-9673
VL - 822
SP - 291
EP - 303
JO - Journal of Chromatography A
JF - Journal of Chromatography A
IS - 2
ER -