0000000000026047

AUTHOR

Athanasios I. Liapis

showing 5 related works from this author

Adsorbents and columns in analytical high-performance liquid chromatography: A perspective with regard to development and understanding

2012

A brief historical survey is presented on the evaluation of silica adsorbents in analytical HPLC. The theory of analytical HPLC is mostly still being based on the height equivalent to a theoretical plate concept and the van Deemter equation that was derived from gas phase adsorption involving a linear adsorption isotherm and fast mass transfer kinetics. One can obviously wonder whether the use of the van Deemter equation is relevant and valid for the evaluation of the performance of HPLC systems, where most often the liquid solutes involve charged molecules in electrolytes and in very many cases the adsorbates are macromolecules having diffusion coefficients of small magnitude. Instead of t…

Van Deemter equationMolecular dynamicsAdsorptionEffective mass (solid-state physics)ChemistryMass transferAnalytical chemistryThermodynamicsFiltration and SeparationTheoretical platePorous mediumPorosityAnalytical ChemistryJournal of Separation Science
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Novel general expressions that describe the behavior of the height equivalent of a theoretical plate in chromatographic systems involving electricall…

2002

Novel general expressions are constructed and presented that describe the behavior of the height equivalent of a theoretical plate (plate height), H, as a function of the linear velocity, Vx, along the axis, x, of the column and the kinetic parameters that characterize the mass transfer and adsorption mechanisms in chromatographic columns. Open tube capillaries as well as columns packed with either non-porous or porous particles are studied. The porous particles could have unimodal or bimodal pore-size distributions and intraparticle convective fluid flow and pore diffusion are considered. The expressions for the plate height, H, presented in this work could be applicable to high-performanc…

ChromatographyChemistryOrganic ChemistryAnalytical chemistryElectro-osmosisGeneral MedicineModels TheoreticalKinetic energyBiochemistryAnalytical ChemistryElectrochromatographyMass transferFluid dynamicsTheoretical plateDiffusion (business)PorosityChromatography High Pressure LiquidJournal of Chromatography A
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The coupling of the electrostatic potential with the transport and adsorption mechanisms in ion-exchange chromatography systems: Theory and experimen…

2005

The coupling of the constitutive expression for the electrostatic potential as specified through Poisson's equation together with the constitutive equations for the mechanisms of convection, diffusion, electrophoretic migration, and adsorption provides the necessary set of constitutive expressions to be employed in the material balance equations of ion-exchange chromatography systems to construct macroscopic continuum models that could be used to design and simulate the dynamic behavior of systems involving a single charged adsorbate or multiple charged adsorbates. A physically relevant and consistent macroscopic continuum model that can predict, as has been observed experimentally by UV co…

Surface diffusionMass transfer coefficientChemistryIon chromatographyConstitutive equationAnalytical chemistryFiltration and SeparationAnalytical ChemistryCondensed Matter::Soft Condensed MatterModeling and simulationMolecular dynamicsAdsorptionChemical physicsMass transferJournal of Separation Science
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Analysis and parametric sensitivity of the behavior of overshoots in the concentration of a charged adsorbate in the adsorbed phase of charged adsorb…

2003

In this work, an analysis of the parametric sensitivity of the overshoot in the concentration of the adsorbate in the adsorbed phase, which occurs under certain conditions during an ion-exchange adsorption process, is presented and used to suggest practical implications of the concentration overshoot phenomenon on operational policies and configurations of chromatographic columns and finite bath adsorption systems. The results presented in this work demonstrate and explain how the development of an overshoot in the concentration of the adsorbate in the adsorbed phase could be enhanced or suppressed by (i) varying the diffusion coefficient, D3, of the adsorbate relative to the diffusion coef…

ChemistryDiffusionAnalytical chemistryLangmuir adsorption modelThermodynamicsElectrolyteCharged particleSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialssymbols.namesakeColloid and Surface ChemistryAdsorptionIonic strengthPhase (matter)symbolsDebye lengthJournal of Colloid and Interface Science
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The effect of the pore structure and zeta potential of porous polymer monoliths on separation performance in ion-exchange mode.

2007

Most often, in bioseparations involving charged macromolecules, the chromatographic systems have low Reynolds and high Peclet numbers. For such systems, an expression is developed and presented in this work for evaluating the throughput in polymeric monoliths where ion-exchange adsorption occurs, as a function of (i) the pressure drop along the length of the monolith, (ii) the functional form and width of the throughpore-size distribution of the monolith, and (iii) the magnitude of the zeta potential on the surface of the throughpores of the monolith. Gaussian and log-normal throughpore-size distributions whose mean throughpore-size and standard deviation values are based on experimentally …

geographygeography.geographical_feature_categoryMonolithic HPLC columnIon exchangeChemistryPolymersIon chromatographyAnalytical chemistryFiltration and SeparationPorosimetryCharged particleAnalytical ChemistryIon ExchangePhase (matter)Zeta potentialMonolithJournal of separation science
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