Franz P. Schmitz
RWTH Aachen University
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Featured researches published by Franz P. Schmitz.
Journal of Supercritical Fluids | 1990
Franz P. Schmitz; Ernst Klesper
Abstract The separation of oligomers and polymers by supercritical fluid chromatography (SFC) is reviewed. Prerequisites for the successful application of SFC to oligomers, such as gradients and the use of suitable mobile and stationary phases, are treated in general terms. The main section covering the separations is largely concerned with oligomers, because the application of SFC to polymers is so far lagging behind. The separations are divided in subsections on hydrocarbon oligomers, vinyl arene oligomers, acrylic acid and acrylate oligomers, oligoethers, condensation type oligomers, miscellaneous oligomers, polymers, and biopolymers. Finally, some problems to which SFC may contribute solutions and problems in the detection of macromolecular substances are discussed.
Journal of Chromatography A | 1984
Dietger Leyendecker; Franz P. Schmitz; Ernst Klesper
Abstract In supercritical fluid chromatography, using dimethyl ether and diethyl ether as eluents, distinct maxima occur in capacity ratios and resolutions at temperatures somewhat above critical when separating polynuclear aromatic hydrocarbons, oligostyrenes or di-alkyl phthalates. They are caused by a decrease in eluent density and the opposing effect of an increase in the substrate vapour pressure. Dimethyl ether allows higher resolutions than diethyl ether. Higher pressures and flow-rates lead to faster analyses but poorer resolution.
Journal of Chromatography A | 1985
Franz P. Schmitz; Heinz Hilgers; Benno Lorenschat; Ernst Klesper
Abstract The chromatographic separation of oligomers prepared from vinyl arene compounds was achieved using eluent gradients with the eluent pair n -pentane-l,4-dioxane, which had previously been applied to oligostyrene separations. Separations were found to occur not only with respect to degree of oligomerization, but also between sub-series of oligomeric species. Transition from the supercritical to the liquid state, which may occur during an eluent gradient run if the selected column temperature is relatively little above T c at the beginning of the gradient, does not seem to reduce the resolution considerably. The combination of two gradient techniques, a pressure gradient and a gradient of eluent composition, was applied for the separation of the difficult to elute N-vinylcarbazole oligomers. Supercritical fluid chromatograms showed considerably superior separation compared with high-performance liquid chromatograms obtained at ambient temperature using the same eluent gradient.
Journal of Chromatography A | 1985
Dietger Leyendecker; Franz P. Schmitz; Dagmar Leyendecker; Ernst Klesper
Abstract The chromatographic behaviour of n-pentane, n-butane, isobutane and propane was studied in the liquid, gaseous and supercritical gaseous states by running chromatograms of a mixture containing four polynuclear aromatic hydrocarbons. Both the capacity ratios and the resolutions reach maxima at temperatures above the boiling or the critical temperature at a given constant pressure. The maxima are the more pronounced the lower the alkane and the higher the molecular weight of the substrate. This temperature-dependent course of resolution at constant pressure is influenced mostly by changes in plate numbers. On increasing the pressure, the capacity ratios and resolution decrease.
Journal of Chromatography A | 1983
Franz P. Schmitz; Ernst Klesper
Abstract The applicability to supercritical fluid chromatography (SFC) of elution by gradients in eluent composition is demonstrated, using alkanes and diethyl ether as the primary eluent and alcohols, cyclohexane and dioxane as the secondary component. For the separation of styrene oligomers, the combination of an alkane with dioxane turned out to be the most efficient. The SFC apparatus used was a modified high-performance liquid chromatographic instrument.
Journal of Supercritical Fluids | 1988
Ernst Klesper; Franz P. Schmitz
Abstract Single and multiple gradient methods that are employed in supercritical fluid chromatography have been reviewed with a special focus on gradients involving temperature, pressure, density, composition, and velocity.
Journal of Chromatography A | 1984
Franz P. Schmitz
Abstract The contributions of the selectivity, α, and plate number, n , to the dependence of chromatographic resolution on the pressure and temperature have been studied. It is demonstrated that these contributions depend on the separation conditions and on the substrates, with changes in α being in some cases responsible for changes in resolution rather than changes in n . Increasing pressure may cause the selectivity to increase, while plate numbers are lowered. For the separation of oligomers, a pressure may be found where a maximum in the overall resolution occurs.
Journal of Supercritical Fluids | 1990
Andre Hütz; Franz P. Schmitz; Dietger Leyendecker; Ernst Klesper
Abstract The effects of the physical factors (temperature, pressure, density, and free volume) on the chromatographic parameters (capacity ratio, selectivity, and resolution) are investigated for supercritical fluid chromatography, using carbon dioxide as the mobile phase, unbonded silica gel as the stationary phase in a packed column, and a mixture of polycyclic aromatic hydrocarbons as the analyte. The results are presented as three-dimensional graphs where color is used to exhibit a fourth variable. Two of the axes in the plots represented the physical parameters whereas the third axis and the color represent chromatographic parameters. By selecting temperature as one of the variables and pressure or density or free volume as the other (which together fully characterize the state of the mobile phase), the dependence of two chromatographic parameters on these variables can be shown and the interrelation between these chromatographic parameters can be illustrated. The interrelations between the chromatographic parameters and the dependence on the physical parameters being more varies in supercritical fluid chromatography then in gas and liquid chromatography, such multidimensional graph are particular value in providing an overview.
Journal of Chromatography A | 1986
Dietger Leyendecker; Dagmar Leyendecker; Franz P. Schmitz; Ernst Klesper
Abstract The influence of temperature, pressure, and density, as well as type and composition of the mobile phase on capacity factors and on resolution was studied. .In general, a shorter analysis time and lower value for the resolutioon were observed when increasing either pressure, density or modifier content or when working at temperatures just below the critical point. However, there are combinations of distinct values for temperature, pressure, and composition, where capacity factors and resolutions reach maximum values. Knowledge of these combinations of values opes a variety of possibilities to optimize separations.
Chromatographia | 1989
B. Gemmel; B. Lorenschat; Franz P. Schmitz
SummarySeveral different oligomers containing polar groups either in the backbone or in the side chains were successfully separated by SFC on polystyrene stationary phases. Composition gradient elution was used, the mobile phase components being CO2 and acetonitrile or CO2 and methanol. Among the oligomers separated were poly(ethylene oxide)s, poly(caprolactone), epoxy prepolymers and poly(2-vinylpyridine). The use of CO2/acetonitrile made possible the detection of ether groups at 190 nm.