Retention mechanism, isocratic and gradient-elution separation and characterization of (co)polymers in normal-phase and reversed-phase high-performance liquid chromatography

被引:63
作者
Jandera, P [1 ]
Holcapek, M [1 ]
Kolárová, L [1 ]
机构
[1] Univ Pardubice, Dept Analyt Chem, Pardubice 53210, Czech Republic
关键词
gradient elution; retention mechanism; polymers; ethylene oxide; propylene oxide;
D O I
10.1016/S0021-9673(99)01216-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Synthetic (co)polymers or (co)oligomers with two (or more) repeating groups show not only molar mass distribution, but also composition and sequence distribution of the individual repeat units. To characterize such two- (or more-) dimensional distribution, liquid chromatography under "critical conditions" has been suggested, where the separation according to one type of repeating units is suppressed by balancing the adsorption and the size-exclusion effects. In present work it is shown that by combination of adequately selected separation conditions in normal-phase and in reversed-phase systems, the two-dimensional distribution mode can be adjusted to result in the separation following the distribution of any of the two repeat units in ethylene oxide-propylene oxide block (co)oligomers. Based on the retention mechanism suggested, prediction and optimization of the conditions for isocratic and gradient-elution separations of (co)oligomers is possible. HPLC-MS with atmospheric-pressure chemical ionization is a Valuable tool for unambiguous identification of the individual (co)oligomers and their tracking in course of method development. Gradient elution can be used for the separation and characterization of block (co)oligomers of ethylene oxide (EO) and propylene oxide (PO) according to the number of the units in one block, while the separation according to the distribution of the units in the other block is suppressed. The effects of the arrangement of the individual EO and PO blocks in the block (co)oligomers (the sequence distribution) affects significantly the retention behavior and the selection of the optimum separation conditions. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:65 / 84
页数:20
相关论文
共 56 条
[41]   DETERMINATION OF DODECYLBENZENESULFONATES AND ETHOXYLATED ALKYLPHENOLS IN LIQUID PESTICIDE FORMULATIONS BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
SCHREUDER, RH ;
MARTIJN, A .
JOURNAL OF CHROMATOGRAPHY, 1988, 435 (01) :73-82
[42]   SURFACTANTS - NON-BIODEGRADABLE, SIGNIFICANT POLLUTANTS IN SEWAGE-TREATMENT PLANT EFFLUENTS - SEPARATION, IDENTIFICATION AND QUANTIFICATION BY LIQUID-CHROMATOGRAPHY, FLOW-INJECTION ANALYSIS MASS-SPECTROMETRY AND TANDEM MASS-SPECTROMETRY [J].
SCHRODER, HF .
JOURNAL OF CHROMATOGRAPHY, 1993, 647 (02) :219-234
[43]   Determination of surfactants in surface water by solid-phase extraction, liquid chromatography and liquid chromatography-mass spectrometry [J].
Scullion, SD ;
Clench, MR ;
Cooke, M ;
Ashcroft, AE .
JOURNAL OF CHROMATOGRAPHY A, 1996, 733 (1-2) :207-216
[44]   ELECTROSPRAY MASS-SPECTROMETRIC ANALYSIS AND PHOTOCATALYTIC DEGRADATION OF POLYETHOXYLATE SURFACTANTS USED IN WOOL SCOURING [J].
SHERRARD, KB ;
MARRIOTT, PJ ;
MCCORMICK, MJ ;
COLTON, R ;
SMITH, G .
ANALYTICAL CHEMISTRY, 1994, 66 (20) :3394-3399
[45]   NONIONIC SURFACTANTS USED AS EXACT MASS INTERNAL STANDARDS FOR THE 700-2100 DALTON MASS RANGE IN FAST ATOM BOMBARDMENT MASS-SPECTROMETRY [J].
SIEGEL, MM ;
TSAO, R ;
OPPENHEIMER, S ;
CHANG, TT .
ANALYTICAL CHEMISTRY, 1990, 62 (04) :322-327
[46]  
SKVORTSOV AM, 1979, POLYM SCI USSR, V21, P371
[47]   LIQUID-CHROMATOGRAPHY FAST-ATOM-BOMBARDEMENT MASS-SPECTROMETRY OF NONIONIC DETERGENTS [J].
TAKEUCHI, T ;
WATANABE, S ;
KONDO, N ;
GOTO, M ;
ISHII, D .
CHROMATOGRAPHIA, 1988, 25 (06) :523-525
[48]  
THRATHNIGG B, 1997, J CHROMATOGR, V761, P21
[49]  
THRATHNIGG B, 1997, J CHROMATOGR A, V791, P21
[50]  
THRATHNIGG B, 1994, J CHROMATOGR A, V665, P47