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Bonded Stationary Phases (bonded + stationary_phase)
Selected AbstractsMobile phase additives for enhancing the chromatographic performance of astaxanthin on nonendcapped polymeric C30 -bonded stationary phasesJOURNAL OF SEPARATION SCIENCE, JSS, Issue 1 2009Philipp Kaiser Abstract Astaxanthin shows peak deformation and reduced peak area response when eluted with methanol and methyl tert -butyl ether on nonendcapped polymeric C30 -bonded HPLC phases. The present study tested different column manufacturers, column batches, and ten mobile phase additives including acids, bases, buffers, complexing and antioxidant agents for improvement of peak shape and peak area response. Concerning chromatographic benefits and feasibility, ammonium acetate was found to be the best additive followed by triethylamine for all columns tested. Variation of the mobile phase pH equivalent and the column temperature showed no synergistic effects on peak shape and peak area response. Results indicate that peak tailing and variation of peak area response are due to different on-column effects. Possible mechanisms of the observed phenomenon will be discussed. [source] Effect of stationary phase polarity on the retention of ionic liquid cations in reversed phase liquid chromatographyJOURNAL OF SEPARATION SCIENCE, JSS, Issue 17 2006Sylwia Kowalska Abstract Chromatographic analysis of ionic liquids on different types of packings offers interesting possibility to determine their retention mechanism. As a consequence, the major interactions between stationary phase ligands and analyzed chemical entities can be defined. The main aim of this work was to analyze cations of ionic liquids on chemically bonded stationary phases with specific structural properties. The attempt to predict the main interactions between positive ions of ionic liquids and stationary phase ligands was undertaken. For that purpose, butyl, octyl, octadecyl, phenyl, aryl, mixed, alkylamide, and cholesterolic packings were chosen and applied to the analysis of six most commonly used ionic liquids' cations. Obtained results indicate mainly dispersive and ,,, type of interaction part in the retention mechanism of analyzed compounds. [source] Synthesis and characterization of chemically bonded stationary phases on hydride surfaces by hydrosilation of alkynes and dienesJOURNAL OF SEPARATION SCIENCE, JSS, Issue 18 2005Joseph J. Pesek Abstract A hydrosilation reaction was used to bind four compounds with one or more alkyne groups or two alkene functionalities. The diffuse reflectance infrared Fourier transform, the 29Si cross-polarization magic-angle spinning (CP-MAS) NMR, and the 13C CP-MAS NMR spectra were used to characterize the various bonded materials. The bonded phase density was determined from carbon elemental analysis. The two ten-carbon hydrophobic stationary phases were characterized chromatographically and static stability tests were run in acidic and basic solutions. [source] Hydride-based silica stationary phases for HPLC: Fundamental properties and applicationsJOURNAL OF SEPARATION SCIENCE, JSS, Issue 15 2005Joseph J. Pesek Abstract Silica hydride is a recent development in chromatographic support materials for HPLC where hydride groups replace 95% of the silanols on the surface. This conversion changes many of the fundamental properties of the material as well as the bonded stationary phases that are the result of further chemical modification of the hydride surface. The general approach for fabricating the silica hydride and subsequent bonded phases is reviewed. Properties of the silica hydride surface are compared to those of the standard material obtained in the preparation of most commercial HPLC stationary phases. Some unique chromatographic properties of hydride-based phases are described as well as some general application areas where these bonded materials may be used in preference to or have advantages not available from typical stationary phases. [source] Evaluation of HPLC columns: A study on surface homogeneity of chemically bonded stationary phasesJOURNAL OF SEPARATION SCIENCE, JSS, Issue 3-4 2003Bogus, aw Buszewski Abstract The aim of the current work is to study the heterogeneity of the adsorbent surface on the basis of physicochemical investigations and chromatographic tests. A series of packing materials with octadecyl chains chemically bonded to a silica matrix were prepared for this purpose. The surface and structural properties of bare silica and silica-based octadecyl phases were characterized by porosimetry, elemental analysis, 29Si CP/MAS NMR, etc. The most advanced characterization methods based on adsorption microcalorimetry (heat of wetting) measurements were employed to obtain information about the heterogeneity and topography of unmodified and modified silica gel. For the chromatographic study, these phases were evaluated on the basis of the retention data under non-aqueous conditions. A test series of solutes with various chemical properties, such as pK a values, was used. It was found that heterogeneity of the packing surface results in low HPLC resolution. Use of a non-aqueous mobile phase (n -hexane) reduces analytical interference by eliminating hydrophobic interactions between alkyl ligands and the analyte. [source] Effect of chemically bonded stationary phases and mobile phase composition on , -blockers retention in RP-HPLCBIOMEDICAL CHROMATOGRAPHY, Issue 3 2009Boguslaw Buszewski Abstract The effects of stationary and mobile phase on retention of 18 , -adrenolytic drugs (, -blockers) have been studied. Four ,deactivated surface' stationary phases (polar-embedded or end-capped) were examined. Special attention was drawn to the cholesterolic (SG-CHOL) and alkylamide (SG-AP) stationary phases, and their application for analysis of the compounds. The retention of analyzed substances was also examined in terms of mobile phase composition. Sixteen different configurations of mobile phases were prepared, all based on methanol and acetonitrile with ammonium acetate and ammonium formate. The difference in retention between ammonium formate and acetate water solutions, and peak shape changes related to the addition of triethylamine (TEA), were investigated. Principal component analysis was used to find the similarities between stationary phases. Polar-embedded phases synthesized on the same sorbent possess very similar properties. All phases based on silica gel compared with the monolithic column also showed similarities in retention of , -blockers. The addition of TEA to the mobile phase did not influence strongly the retention, and analysis of asymmetry factors showed only a little peak broadening for a few compounds on the monolithic column. Copyright © 2008 John Wiley & Sons, Ltd. [source] | ||||||||||