Search results for "Resolution"
showing 10 items of 1928 documents
Resolution assessment and performance of several organic modifiers in hybrid micellar liquid chromatography
2001
The performance of four criteria that measure the elementary resolution (modified selectivity, modified RS, peak purity, and orthogonal valley-to-peak ratio) was critically assessed using as global resolution function, the product of elementary measurements. The peak purities and valley-to-peak criteria yielded the best description of the overall separation according to the shape of the resolution surfaces compared to the peak arrangements in the chromatograms, the capability of defining unambiguously the composition regions of complete resolution, and the resolution achieved in the predicted optimums. Peak purities were used to compare the effect of five organic modifiers (1-propanol, 1-bu…
Determination of water-soluble vitamins in energy and sport drinks by micellar electrokinetic capillary chromatography
2016
Abstract A method for the determination of water-soluble vitamins in several energy and sport drinks by micellar electrokinetic chromatography (MEKC) has been developed in this work. The separation of vitamins was studied in terms of background electrolyte composition (borate content, pH, surfactant type and content) and in other MEKC parameters. A study of the possible compounds found in the vitamin-enriched drinks that could interfere in vitamin determination was also performed, and a modified procedure with enhanced resolution was developed. The proposed method was successfully applied to the analysis of water-soluble vitamins in a variety of energy and sport drinks and also in fruit nec…
On the Measurement of Dead Time in Micellar Liquid Chromatography
1996
Abstract Modelling of the retention of solutes in micellar liquid chromatography allows the optimization of the resolution of a mixture of solutes and the determination of physico-chemical retention parameters. Both tasks imply the calculation of capacity factors, which are severely affected by the value of dead time. However, the determination of the dead time is not easy when a micellar mobile phase is used owing to the wide and variable perturbations that appear at the heads of the chromatograms. Four different criteria of determination of a reference time in the chromatograms are proposed and compared. The criteria are applied to mobile phases containing a varying concentration of surfa…
Optimization of the phase system in the analysis of polynuclear aromatics (PNA) from diesel engine exhaust by high performance liquid chromatography …
1979
Polynuclear aromatics (PNA) were collected and enriched from diesel engine exhausts by means of a probe and an absorber system. Group separation of PNA from other constituents of exhaust was accomplished through elution with n-heptane on a silica column. A variety of phase systems ranging from unpolar to strong polar packings and eluents, respectively, were tested to resolve PNA into single species. Of these a n-octadecyl bonded silica packing and methanol/water was found to be the most optimal with regard to resolution for real PNA mixtures. Separation was completed within 2–3 h at isocratic conditions.
Limits of multi-linear gradient optimisation in reversed-phase liquid chromatography
2005
Abstract The concept of limiting peak purity was applied to quantify the degree of completion of the separation capability of a chromatographic system using multi-linear gradients. The objective was to check whether the complexity of a gradient program deserves be increased to enhance resolution by inserting more linear segments, or on the contrary, no significant improvements can be expected under more complex gradients. A set of 19 isoindole derivatives of primary amino acids was selected to test the performance of isocratic, single linear and multi-linear gradients. Accurate simulated chromatograms were obtained via numerical integration of the general equation of gradient elution, using…
Protocol to compare column performance applied to hydrophilic interaction liquid chromatography
2019
Abstract The lack of retention of highly polar solutes in liquid chromatography with reversed phase columns (RPLC) can be solved through the use of the hydrophilic interaction liquid chromatographic (HILIC) mode. Due to the complexity of the separation mechanisms in HILIC and the different factors that may have significant influence, the selection of the appropriate stationary phase plays a fundamental role in the development of analytical procedures to obtain good performance. In this work, the chromatographic performance of bare silica and six polar stationary phases with different functionalized groups (with neutral, cationic, anionic and zwitterionic character) are investigated. The beh…
Gas chromatographic and mass spectrometric analysis of bile acids as trifluoroacetyl-hexafluoroisopropyl and heptafluorobutyryl derivatives
1981
Abstract The gas chromatographic retention times on QF-1 of 38 bile acids in the form of their trifluoroacetyl-hexafluoroisopropyl (TFA-HFIP), trifluoroacetyl-methyl, and heptafluorobutyryl derivatives are given. In general hexafluoroisopropyl ester trifluoroacetates proved superior with regard to simplicity of preparation, absence of artifacts, and resolution on QF-1. The main disadvantages of heptafluorobutyrates were the production of artifacts with some ketonic bile acids and the impossibility of separating any of the dihydroxy bile acids with substituents in the 3,6- and 3,7-positions. Mass spectra of TFA-HFIP derivatives were recorded with both direct and gas chromatographic inlet sys…
H-point standard additions method for resolution of overlapped chromatographic peaks with a conventional fluorescence detector. Determination of phen…
1996
The H-Point Standard Additions Method (HPSAM) is proposed in order to resolve overlapping peaks in liquid chromatography by using a conventional fluorescence detector. The method uses as analytical signals the heights or the areas obtained at two previously selected emission wavelengths, and good results are obtained for highly overlapping peaks with highly overlapping fluorescence spectra. The principal benefits of the method are the ease of finding the required wavelengths, its insensitivity to changes in the retention time of the peak from one injection to another, and the possibility of using it in highly or only partially overlapping peaks. We have applied the method to the determinati…
Packings and stationary phases for biopolymer separations by HPLC
1987
Packings and stationary phases applied to high resolution separations of proteins, enzymes, and nucleic acids must satisfy a series of distinct criteria that are different from those usually required by HPLC of low molecular weight non-biologically active analytes. These requirements have been met through substantial improvements in classical gel media together with novel developments in silica supports, and have led to a family of products with tailor-made and reproducible properties. Supports consisting of cross-linked organic gels, and inorganic materials (mostly silicas) are now available with graduated particle sizes, pore sizes, porosities and surface areas as well as non-porous beads…
Global treatment of chromatographic data with MICHROM
1997
Abstract The program MICHROM for the general treatment of chromatographic data is presented. MICHROM takes part in all the stages of the analytical process. It allows determination of dead time, smoothing of chromatograms, measurement of peak parameters, fitting of skewed peaks, and deconvolution of overlapped peaks. Tools for the experimental design, optimization of the mobile phase composition to resolve a mixture of analytes, and simulation of chromatograms in several experimental conditions, are implemented. Routines for the graphical representation of chromatograms, resolution surfaces, contour maps, management of data series, optimization and regression analysis, are also included. Th…