Search results for "Elution"

showing 10 items of 337 documents

Some observations on the prediction of retention in reversed-phase liquid chromatography using the pH as main factor

2004

Abstract When solutes show acid–base behaviour inside the working pH of a reversed-phase liquid chromatographic (RPLC) column, besides the type and percentage of organic modifier, pH can be included to improve the possibilities of separation. Optimisation based on a retention model is an economical and reliable way to achieve the best resolution. However, the difficulties found in knowing the exact pH values and the dependence of acid−base constants of solutes with mobile phase composition makes the accurate modelling of the retention behaviour as a function of these variables rather difficult. In this work, it is shown that in fact, there is no need to have this information. Based on the e…

Work (thermodynamics)Aqueous solutionChromatographyChemistryElutionReversed-phase chromatographyBuffer solutionBiochemistryAnalytical Chemistrychemistry.chemical_compoundPhase (matter)Yield (chemistry)Environmental ChemistryAcetonitrileSpectroscopyAnalytica Chimica Acta
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Estimation of peak capacity based on peak simulation.

2018

Peak capacity (PC) is a key concept in chromatographic analysis, nowadays of great importance for characterising complex separations as a criterion to find the most promising conditions. A theoretical expression for PC estimation can be easily deduced in isocratic elution, provided that the column plate count is assumed constant for all analytes. In gradient elution, the complex dependence of peak width with the gradient program implies that an integral equation has to be solved, which is only possible in a limited number of situations. In 2005, Uwe Neue developed a comprehensive theory for the calculation of PC in gradient elution, which is only valid for certain situations: single linear …

Work (thermodynamics)ChromatographyChromatographyChemistryElutionGaussian010401 analytical chemistryOrganic ChemistryMathematical analysisProbabilistic logicGeneral Medicine010402 general chemistry01 natural sciencesBiochemistryIntegral equationExpression (mathematics)0104 chemical sciencesAnalytical Chemistrysymbols.namesakeModels ChemicalsymbolsComputer SimulationAlgebraic expressionConstant (mathematics)Journal of chromatography. A
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The Fractal Approach to Secondary Mechanisms in SEC

2007

Abstract Size‐exclusion chromatography (SEC) is one of the most used experimental techniques to characterize polymers in solution; it has been applied to interpret the elution behaviour of many polymer‐solvent systems in five types of column packings. The experimental data have revealed that the classical universal calibration is not accomplished. Deviations from a unique curve are a consequence of two effects: entropic (exclusion by size) and enthalpic (binary and ternary interactions between solvent, polymer, and gel), which results in secondary mechanisms accompanying the main “ideal” SEC separation mechanism. Therefore, three approaches of building a calibration curve have been compared…

Work (thermodynamics)ChromatographyElutionCalibration curveChemistryCalibration (statistics)Clinical BiochemistryPharmaceutical ScienceBiochemistryAnalytical ChemistryGel permeation chromatographyFractalMolar mass distributionTernary operationJournal of Liquid Chromatography & Related Technologies
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Extension of the linear solvent strength retention model including a parameter that describes the elution strength changes in liquid chromatography.

2020

Modelling the retention behaviour of solutes in liquid chromatography, based on the composition of the mobile phase is a common task in the chromatographic practice. Along the development of liquid chromatography (LC), several models have been proposed to help in understanding the retention mechanisms, and especially, allow the prediction of retention times with optimisation purposes. Particular models are used for different LC modes, such as normal phase (NPLC), reversed phase (RPLC), hydrophilic interaction (HILIC), and micellar (MLC). In this work, a general equation is proposed that includes a parameter (the elution degree, g), which characterises the way the elution strength varies wit…

Work (thermodynamics)ChromatographyElutionChemistryHydrophilic interaction chromatographyNormal phase010401 analytical chemistryOrganic ChemistryGeneral Medicine010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesAnalytical ChemistrySolvent strengthModels ChemicalGeneral equationPhase (matter)SolventsGradient elutionHydrophobic and Hydrophilic InteractionsChromatography LiquidJournal of chromatography. A
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Enhancement in the computation of gradient retention times in liquid chromatography using root-finding methods.

2019

Abstract Gradient elution may provide adequate separations within acceptably short times in a single run, by gradually increasing the elution speed. Similarly to isocratic elution, chromatograms can be predicted under any experimental condition, through strategies based on retention models. The most usual approach implies solving an integral equation (i.e., the fundamental equation of gradient elution), which has an analytical solution only for certain combinations of retention model and gradient programme. This limitation can be overcome by using numerical integration, which is a universal approach although at the cost of longer computation times. In this work, several alternatives to impr…

Work (thermodynamics)ChromatographyIsocratic elutionChemistryElutionComputation010401 analytical chemistryOrganic ChemistryGeneral Medicine010402 general chemistry01 natural sciencesBiochemistryIntegral equation0104 chemical sciencesAnalytical ChemistryNumerical integrationGradient elutionRoot-finding algorithmAlgorithmsChromatography LiquidJournal of chromatography. A
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Enhanced calculation of optimal gradient programs in reversed-phase liquid chromatography

2003

Abstract The resolution of a mixture of 16 β-blockers under gradient elution was optimised using both isocratic and gradient training sets, with a reversed-phase column and acetonitrile–water eluents. Error theory was applied to measure the information extracted from different gradient experimental designs. This allows checking the expected accuracy when gradient predictions exceed the initial solvent concentrations tested in the training set. This work applies the results on modelling found in a previous study [J. Chromatogr. A 1018 (2003) 169] where the performance of several retention models was compared. Enhanced retention predictions were applied to the optimisation of gradient program…

Work (thermodynamics)ChromatographyResolution (mass spectrometry)ChemistryElutionDesign of experimentsOrganic ChemistryAnalytical chemistryGeneral MedicineReversed-phase chromatographyCurvatureBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryChromatography High Pressure LiquidSpectral purityJournal of Chromatography A
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Peak dispersion in gradient elution: An insight based on the plate model.

2020

Gradient elution in liquid chromatography reduces the analysis time, improves the efficiency and increases the peak capacity. The study of this chromatographic mode has been based mainly on kinetic dispersion models. The plate model has been applied to a lesser extent, despite being the basis for the concepts of plate height and chromatographic efficiency. In this work, a general equation describing peak dispersion in HPLC gradient elution is derived from the plate model. This equation is studied and validated for three types of gradients: (i) a reference gradient without ramp in which the retention factor varies with time identically throughout the column, (ii) a gradient of stationary pha…

Work (thermodynamics)Differential equation010402 general chemistryKinetic energy01 natural sciencesBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryPressureChromatography High Pressure LiquidChromatographyChemistryElution010401 analytical chemistryOrganic ChemistryGeneral MedicineMechanicsCompression (physics)0104 chemical sciencesKineticsModels ChemicalLinear ModelsSolventsIndicators and ReagentsDispersion (chemistry)Constant (mathematics)Journal of chromatography. A
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Peak capacity estimation in isocratic elution.

2008

Peak capacity (i.e. maximal number of resolved peaks that fit in a chromatographic window) is a theoretical concept with growing interest, but based on a situation rarely met in practice. Real chromatograms tend to have uneven distributions, with overlapped peaks and large gaps. The number of resolved compounds should, therefore, be known from estimations. Several equations have been reported for this purpose based on three perspectives, namely, the intuitive approach (peak capacity as the size of the retention time window measured in peak width units), which assumes peaks with the same width, and the outlines of Giddings and Grushka, which consider changes in peak width with retention time…

Work (thermodynamics)Isocratic elutionChromatographyAcetonitrilesChemistryOrganic ChemistryMean valueAdrenergic beta-AntagonistsChromatography liquidSodium Dodecyl SulfateGeneral MedicineModels TheoreticalBiochemistryAnalytical ChemistrySkewnessPhase compositionDiureticsRetention timeMicellesChromatography LiquidJournal of chromatography. A
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Some insights on the description of gradient elution in reversed-phase liquid chromatography

2014

The so-called "fundamental equation for gradient elution" has been used for modeling the retention in gradient elution. In this approach, the instantaneous retention factor (k) is expressed as a function of the change in the modifier content (φ(ts )), ts being the time the solute has spent in the stationary phase. This approach can only be applied at constant flow rate and with gradients where the elution strength depends on the column length following a f(t-l/u) function, u being the linear mobile phase flow rate, and l the distance from the column inlet to the location where the solute is at time t measured from the beginning of the gradient. These limitations can be solved by using the h…

Work (thermodynamics)Quadratic equationChemistryElutionPhase (matter)Content (measure theory)Analytical chemistryThermodynamicsFiltration and SeparationFunction (mathematics)Reversed-phase chromatographyAnalytical ChemistryVolumetric flow rateJournal of Separation Science
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Prefractionation of aroma extracts from fat-containing food by high-performance size-exclusion chromatography

1996

A method for the prefractionation of aroma extracts of fat-containing food using high-performance size-exclusion chromatography is presented. The aim was to obtain a fraction of volatile compounds with a residual triglyceride content as low as possible, in order to allow its direct analysis by gas chromatography. Two different mobile phases, diethyl ether and dichloromethane, were tested and the elution volumes of triglycerides and a large variety of aroma compounds were measured. The quality of separation between triglycerides and volatile compounds as a function of column load was studied. The method was successfully applied to the analysis of goat cheese volatiles.

[CHIM.ANAL] Chemical Sciences/Analytical chemistryChromatographybiology010405 organic chemistryElution010401 analytical chemistryOrganic ChemistrySize-exclusion chromatographyFraction (chemistry)General Medicinebiology.organism_classification01 natural sciencesBiochemistry0104 chemical sciencesAnalytical ChemistryGel permeation chromatographychemistry.chemical_compoundchemistry[CHIM.ANAL]Chemical Sciences/Analytical chemistryGas chromatographyDiethyl etherComputingMilieux_MISCELLANEOUSAromaDichloromethaneJournal of Chromatography A
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