Characterisation of the chromatographic properties of a silica–polypyrrole composite stationary phase by inverse liquid chromatography
Silica–polypyrrole particles have been used as a composite stationary phase for liquid chromatography. Determination of capacity factors ( k′) of a wide number of polycyclic aromatic hydrocarbon (PAH) molecular probes allows the characterisation of the chromatographic properties of the silica–polypy...
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Published in | Journal of Chromatography A Vol. 969; no. 1; pp. 167 - 180 |
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Main Authors | , , , |
Format | Journal Article Conference Proceeding |
Language | English |
Published |
Amsterdam
Elsevier B.V
06.09.2002
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | Silica–polypyrrole particles have been used as a composite stationary phase for liquid chromatography. Determination of capacity factors (
k′) of a wide number of polycyclic aromatic hydrocarbon (PAH) molecular probes allows the characterisation of the chromatographic properties of the silica–polypyrrole stationary phase. Capacity factors in the range of 0.10 up to 6.1 were determined, thus demonstrating the high affinity of the PAH probes towards the stationary phase. The selectivity of the composite stationary phase was also evaluated as a function of the planarity of the molecular probes injected. Capacity factors determined for PAHs (two-dimensional molecular probes) are higher than those measured for phenyl-substituted PAHs (phenyl-PAHs, three-dimensional molecular probes). Determination of capacity factors, dependence on the composition of the mobile phase demonstrates the reverse α-phase properties of the composite stationary phase. The acid–base properties of the composite silica–polypyrrole stationary phase were investigated using benzene derivative molecular probes (i.e., toluene, phenol, benzoic acid and aniline). Capacity factors in the range of 0.45 to 1.0 were determined. This study clearly demonstrates that this composite stationary phase exhibits selective interactions towards PAHs and phenyl-substituted PAHs and strong acid–base properties depending on the structure, the geometry and the acid–base properties of the molecular probes eluted. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0021-9673 |
DOI: | 10.1016/S0021-9673(02)00379-5 |