TY - JOUR
T1 - Separation of selected humic degradation compounds by capillary electrochromatography with monolithic and packed columns
AU - Ping, Guichen
AU - Schmitt-Kopplin, Philippe
AU - Hertkorn, Norbert
AU - Zhang, Weibing
AU - Zhang, Yukui
AU - Kettrup, Antonius
PY - 2003/3
Y1 - 2003/3
N2 - The separation of selected lignin/humic substance (HS) degradation compounds by capillary electrochromatography (CEC) with a methacrylate-based monolithic column and a conventional column packed with 5 μm octadecyl silica (ODS) particles is presented. The effects of organic modifier concentration, pH of the mobile phase, ionic strength, applied voltage, and temperature on the separation were investigated to determine the optimal separation conditions. With the increase of pH in the mobile phase, some of analytes start to ionize and both chromatographic partition and electrophoresis can play roles in separation simultaneously. Accordingly, different selectivity from high-performance liquid chromatography (HPLC) and capillary electrophoresis (CE) could be achieved. The performances of both kinds of columns were compared. The results showed that the peaks of compounds obtained on the former column were much wider than those on the latter one, although good separation efficiency of alkylbenzenes could be readily achieved; the most probable reasons for this behavior and method to solve this problem were briefly discussed. The CEC of a soil fulvic acid with a monolithic column produced partly resolved broad bands; by means of nuclear magnetic resonance (NMR) analysis a wide range of oxygen derived aromatic substitution patterns was found with prominent contributions from phenolic and carboxylic groups.
AB - The separation of selected lignin/humic substance (HS) degradation compounds by capillary electrochromatography (CEC) with a methacrylate-based monolithic column and a conventional column packed with 5 μm octadecyl silica (ODS) particles is presented. The effects of organic modifier concentration, pH of the mobile phase, ionic strength, applied voltage, and temperature on the separation were investigated to determine the optimal separation conditions. With the increase of pH in the mobile phase, some of analytes start to ionize and both chromatographic partition and electrophoresis can play roles in separation simultaneously. Accordingly, different selectivity from high-performance liquid chromatography (HPLC) and capillary electrophoresis (CE) could be achieved. The performances of both kinds of columns were compared. The results showed that the peaks of compounds obtained on the former column were much wider than those on the latter one, although good separation efficiency of alkylbenzenes could be readily achieved; the most probable reasons for this behavior and method to solve this problem were briefly discussed. The CEC of a soil fulvic acid with a monolithic column produced partly resolved broad bands; by means of nuclear magnetic resonance (NMR) analysis a wide range of oxygen derived aromatic substitution patterns was found with prominent contributions from phenolic and carboxylic groups.
KW - Capillary electrochromatography
KW - Correlation spectroscopy
KW - Heteronuclear single quantum coherence
KW - Humic substance
KW - Lignin degradation products
KW - Monolithic columnn
KW - Nuclear magnetic resonance
KW - Reversed-phase
UR - http://www.scopus.com/inward/record.url?scp=0037949372&partnerID=8YFLogxK
U2 - 10.1002/elps.200390139
DO - 10.1002/elps.200390139
M3 - Article
C2 - 12658683
AN - SCOPUS:0037949372
SN - 0173-0835
VL - 24
SP - 958
EP - 969
JO - ELECTROPHORESIS
JF - ELECTROPHORESIS
IS - 6
ER -