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Alan P Sweeney

Publications and source records attributed to Alan P Sweeney.

4 recordsLinked to original sources

Viscous fingering induced flow instability in multidimensional liquid chromatography.

Viscous fingering is a flow instability phenomenon that results in the destabilisation of the interface between two fluids of differing viscosities. The destabilised interface results in a complex mixing of the two fluids in a pattern that resembles fingers. The conditions that enhance this type of flow instability can be found in coupled chromatographic separation systems, even when the solvents used in each of the separation stages have seemingly similar chemical and physical properties (other than viscosity). For example, the viscosities of acetonitrile and methanol are sufficiently different that instability at the interface between these two solvents can be established and viscous fingering results. In coupled chromatographic systems, the volume of solvent transported from one separation dimension to the second often exceeds the injection volume by two or more orders of magnitude. As a consequence, viscous fingering may occur, when otherwise following the injection of normal analytical size injection plugs viscous fingering would not occur. The findings in this study illustrate the onset of viscous fingering in emulated coupled chromatographic systems and show the importance of correct solvent selection for optimum separation performance.

Acetonitriles↗

Using analytical multidimensional isocratic HPLC methods of separation to isolate active constituents in natural products.

Multidimensional reversed-phase HPLC was employed to isolate the active constituents from a crude extract of Clerodendrum floribundum R. Br. These active constituents were known to have bioactivity against the enzyme xanthine oxidase and potentially could be employed in the treatment of gout. Using a multidimensional separation approach, rapid isolation of the active constituents was achieved from a complex sample matrix. As each separation dimension was isocratic, no equilibration time was required and consequently the technique shows promise in the scale up to preparative levels where high throughput is important.

Biological Products↗

Comprehensive coupled reversed-phase reversed-phase separations of a complex isomeric mixture.

Using predictions based on results obtained from Information Theory and Factor Analysis for the two-dimensional separation of a complex isomeric mixture, a practical experimental comprehensive coupled reversed phase-reversed phase chromatographic system was developed. In total four reversed phase-reversed phase systems were studied, each of which theory predicted would be able to resolve essentially equal numbers of components. However, in practice only one of these coupled systems realised the theoretical potential. This system employed as the first dimension, a C18 stationary phase with methanol as the mobile phase and as the second dimension, carbon clad zirconia as the stationary phase and acetonitrile as the mobile phase. In this system, 27 of the 32 isomers of a mixture of oligostyrenes were resolved. Failure of the remaining coupled systems to achieve the theoretical potential was attributed to high solute crowding, low efficiency of separation space utilisation and long analysis times in the second dimension.

Journal Article↗

Development of a two-dimensional liquid chromatography system with trapping and sample enrichment capabilities.

A two-dimensional HPLC system was developed where "heart-cutting" chromatography, in conjunction with cold temperature trapping, was used to isolate and concentrate specific sample analytes. Low molecular mass polystyrene oligomers were used as model compounds to illustrate the operation of the instrument and evaluate the performance of the trapping system. A critical factor in the operation of the trapping system was the relative degree of retention between the first column and the trapping column. The results of this study showed that up to 32 consecutive heart-cut fractions from the first separation dimension could be stored in a trapping column with good analyte recovery and without significant loss in resolution upon elution on the second separation dimension.

Chromatography, High Pressure Liquid↗