Predicting the chromatographic retention of polymers: Application of the polymer model to poly(styrene/ethylacrylate)copolymers

被引:10
|
作者
Bashir, Mubasher A. [1 ]
Radke, Wolfgang [1 ]
机构
[1] German Inst Polymers, Deutsch Kunststoff Inst, D-64289 Darmstadt, Germany
关键词
Polymer chromatography; Retention models; Size exclusion chromatography; Critical chromatography; Adsorption chromatography; Gradient chromatography; Statistical copolymers; PHASE LIQUID-CHROMATOGRAPHY; GRADIENT SEPARATION; POLYETHYLENE-GLYCOL; COPOLYMER RETENTION; BLOCK-COPOLYMERS; CRITICAL-POINT; MACROMOLECULES; ADSORPTION; MECHANISM; BEHAVIOR;
D O I
10.1016/j.chroma.2011.12.062
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The retention behavior of a range of statistical poly(styrene/ethylacrylate) copolymers is investigated, in order to determine the possibility to predict retention volumes of these copolymers based on a suitable chromatographic retention model. It was found that the composition of elution in gradient chromatography of the copolymers is closely related to the eluent composition at which, in isocratic chromatography, the transition from elution in adsorption to exclusion mode occurs. For homopolymers this transition takes place at a critical eluent composition at which the molar mass dependence of elution volume vanishes. Thus, similar critical eluent compositions can be defined for statistical copolymers. The existence of a critical eluent composition is further supported by the narrower peak width, indicating that the broad molar mass distribution of the samples does not contribute to the retention volume. It is shown that the existing retention model for homopolymers allows for correct quantitative predictions of retention volumes based on only three appropriate initial experiments. The selection of these initial experiments involves a gradient run and two isocratic experiments, one at the composition of elution calculated from first gradient run and second at a slightly higher eluent strength. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:107 / 112
页数:6
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