Search results for "Porous membrane"

showing 10 items of 12 documents

Immunochromatographic Assay for Quantitation of Milk Progesterone.

1996

We describe a rapid immunochromatographic method for the quantitation of progesterone in bovine milk. The method is based on a 'competitive' assay format using the monoclonal antibody to progesterone and a progesterone-protein conjugate labelled with colloidal gold particles. The monoclonal antibody to progesterone is immobilized as a narrow detection zone on a porous membrane. The sample is mixed with colloidal gold particles coated with progesterone-protein conjugate, and the mixture is allowed to migrate past the detection zone. Migration is facilitated by capillary forces. The amount of labelled progesterone-protein conjugate bound to the detection zone, as detected by photometric scann…

Detection limitBovine milkChromatographymedicine.drug_classCapillary actionChemistryGeneral Chemical EngineeringAntibodies MonoclonalCross ReactionsMonoclonal antibodySensitivity and SpecificityChromatography AffinityMilkColloidal goldPorous membranemedicineAnimalsCattleChromatography Thin LayerProgesteroneConjugateActa Chemica Scandinavica
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Ion size effects on the electrokinetic flow in nanoporous membranes caused by concentration gradients

2003

The space charge model (SCM) relies on the Poisson−Boltzmann (PB) equation, and hence on the assumption of negligible ion size effects, to calculate the radial distribution of the electrical potent...

Electrokinetic phenomenaChemistryFlow (psychology)Materials ChemistryAnalytical chemistryRadial distributionNanoporous membranePhysical and Theoretical ChemistryConcentration gradientSpace chargeSurfaces Coatings and FilmsIon
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THE GOLDMAN CONSTANT FIELD ASSUMPTION - SIGNIFICANCE AND APPLICABILITY CONDITIONS

1986

Ionic transport phenomena in simple, porous membranes can be approximately represented by the Nernst-Planck flux equations and Poisson's equation. In order to solve this set of equations for each particular case, the Goldman constant field assumption is one of the most widely used. In the present paper the significance and the applicability conditions of the above hypothesis is critically examined. and the particular situations where it is exact are shown. These conditions are later verified by solving numerically the electrodiffusion equations. The analysis carried out shows that some of the earlier studies based on asymptotic expansions and numerical solutions should be partially revised.

General Chemical EngineeringFluxConstant fieldPoisson distributionSet (abstract data type)symbols.namesakeSimple (abstract algebra)Porous membranesymbolsApplied mathematicsStatistical physicsDiffusion (business)Transport phenomenaMathematics
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IONIC TRANSPORT ACROSS POROUS CHARGED MEMBRANES AND THE GOLDMAN CONSTANT FIELD ASSUMPTION

1986

Starting from a simple theoretical model based on Nernst-Planck flux equations and the Donnan equilibrium relationship, the ionic transport across a porous, charged membrane is analysed and conditions are given which make exact the so-called “constant field assumption”. The validity of the reported results is later verified in the case of a well-known problem: the ionic transport across a cation-exchange membrane under bi-ionic conditions.

MembraneChemistryGeneral Chemical EngineeringPorous membraneDiffusionPhysics::Atomic and Molecular ClustersAnalytical chemistryIonic bondingFluxThermodynamicsConstant fieldIon transferPorosity
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A real time immunoassay in alumina membranes

2014

To date, photonic biosensing with porous membranes has produced slow responses and long sensing times, due to the narrow (less than 100 nm) closed end pores of the membranes used. Recently, polarimetry was used to demonstrate analyte flow through, and real time biosensing in, free-standing porous alumina membranes. Here, we demonstrate how an improved functionalization technology, has for the first time enabled a real-time immunoassay within a porous membrane with a total assay time below one hour. With the new approach, we show a noise floor for individual biosensing measurements of 3.7 ng/ml (25 pM), and a bulk refractive index detection limit of 5×10-6 RIU, with a standard deviation of l…

Other Electrical Engineering Electronic Engineering Information EngineeringMaterials sciencemedicine.diagnostic_testbusiness.industryAlumina membranesNanotechnologyMembraneporous aluminaQuantum dotPorous membraneImmunoassayCopolymermedicineAnnan elektroteknik och elektronikPhotonicsbusinessBiosensorBiosensorIEEE SENSORS 2014 Proceedings
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Preparation of pH sensitive poly(vinilydenefluoride) porous membranes by grafting of acrylic acid assisted by supercritical carbon dioxide

2012

Free radical grafting of acrylic acid (AA) on poly(vinilydenefluoride) (PVDF) porous membranes was studied at 65°C using supercritical carbon dioxide (scCO 2) as a solvent and delivery agent. The process was initiated by the thermal decomposition of benzoylperoxide (BPO). Spectroscopic analyses confirmed the presence of poly(AA) chains linked to treated membranes. The mass fraction of grafted AA increased with grafting time and BPO concentration while it decreased when the density of the fluid phase was enhanced. A not-monotonic trend was obtained when the effect of the initial AA concentration was studied. The grafting process was accompanied by a reduction of the crystallinity of the PVDF…

PH-dependentGrafting proceGeneral Chemical EngineeringRadical polymerizationpH-sensitive polymersMass fractionPoly(vinylidene fluoride)Free radical graftingGrafting degreeCarboxylic acidRelease experimentAcrylic acidSupercritical fluid extraction Grafting (chemical)chemistry.chemical_compoundCrystallinityPVDF membraneFree radicalPolymer chemistrypH sensorPhysical and Theoretical ChemistryFluid-phasepH sensitiveAcrylic acidCrystallinitieDecompositionSupercritical carbon dioxideFree radical polymerizationChemistrySupercritical carbon dioxides Carbon dioxideSettore ING-IND/27 - Chimica Industriale E TecnologicaCondensed Matter PhysicsGraftingSolventMembraneSpectroscopic analysiPorous membraneNuclear chemistryThe Journal of Supercritical Fluids
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Pore structure and function of synthetic nanopores with fixed charges: tip shape and rectification properties

2011

We present a complete theoretical study of the relationship between the structure (tip shape and dimensions) and function (selectivity and rectification) of asymmetric nanopores on the basis of previous experimental studies. The theoretical model uses a continuum approach based on the Nernst-Planck equations. According to our results, the nanopore transport properties, such as current-voltage (I-V) characteristics, conductance, rectification ratio, and selectivity, are dictated mainly by the shape of the pore tip (we have distinguished bullet-like, conical, trumpet-like, and hybrid shapes) and the concentration of pore surface charges. As a consequence, the nanopore performance in practical…

Quantitative Biology::BiomoleculesPhysics::Biological PhysicsNanostructureMaterials scienceMechanical EngineeringConductanceBioengineeringNanotechnologyGeneral ChemistryConical surfaceStructure and functionQuantitative Biology::Subcellular ProcessesNanoporeRectificationMechanics of MaterialsChemical physicsGeneral Materials ScienceSurface chargeNanoporous membraneElectrical and Electronic EngineeringNanotechnology
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Protein diffusion through charged nanopores with different radii at low ionic strength

2014

[EN] The diffusion of two similar molecular weight proteins, bovine serum albumin (BSA) and bovine haemoglobin (BHb), through nanoporous charged membranes with a wide range of pore radii is studied at low ionic strength. The effects of the solution pH and the membrane pore diameter on the pore permeability allow quantifying the electrostatic interaction between the chargedpore and the protein. Because of the large screening Debye length, both surface and bulk diffusion occur simultaneously. By increasing the pore diameter, the permeability tends to the bulk self-diffusion coefficient for each protein. By decreasing the pore diameter, the charges on the pore surface electrostatically hinder …

Self assembled monolayersUltrafiltration membranesSurface PropertiesPHStatic ElectricityAnalytical chemistryGeneral Physics and AstronomyDiffusionHemoglobinsNanoporessymbols.namesakeProtein purificationAnimalsHemoglobinParticle SizePhysical and Theoretical ChemistryBovine serum albuminMolecular transportAqueous solutionsSerum AlbuminDebye lengthChemical PhysicsbiologyNanoporousChemistryOsmolar ConcentrationMicroporous membranesLight scatteringSerum Albumin BovineBovineHydrogen-Ion ConcentrationSurfaceNanoporeMembraneIsoelectric pointBovine serum albuminPermeability (electromagnetism)Chemical physicsFISICA APLICADAPhysical SciencesChemical Sciencesbiology.proteinsymbolsCattlePorosity
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CHARACTERIZATION OF HYDROPHOBIC POLYMERIC MEMBRANES FOR MEMBRANE DISTILLATION PROCESS

2010

Hydrophobic microporous membranes are utilized in membrane distillation (MD) processes, e.g. seawater desalination at moderate temperatures. The vapour permeability of commercial hydrophobic membranes with different pore sizes (0.2-1 micron) was characterized through a simple apparatus designed-on-purpose. A cylindrical vessel had a face closed by the membrane and the other connected to a thin graduate tube. The water level variation in the tube is recorded and related to the vapour flux across the membrane. Measurements were taken in the temperature range 20-80°C. A fan tangential to membrane surface was employed to maintain a constant driving force for vapour transport. Vapour flux did no…

Settore ING-IND/24 - Principi Di Ingegneria ChimicaSettore ING-IND/26 - Teoria Dello Sviluppo Dei Processi ChimiciChemistrySeawater desalinationSynthetic membraneMembrane distillation hydrophobic membranesMembrane distillationCharacterization (materials science)MembraneSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiChemical engineeringMicroporous membranesScientific methodOrganic chemistryGeneral Materials SciencePolymeric membrane
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Validity of the electroneutrality and goldman constant-field assumptions in describing the diffusion potential for ternary electrolyte systems in sim…

1986

Abstract Three numerical algorithms capable of simulating transport processes through simple, porous membranes in the steady state have been employed in order to study the change in the diffusion potential with the membrane thickness and the ionic concentrations for the ternary systems NaClHClH20 and CaCI2NaC1H 2 O. The first simulation procedure uses Poisson's equation, the two others replace this equation by the electroneutrality and Goldman constant-field approximations respectively. From the results presented here, conditions for the applicability of the electroneutrality and constantfield assumption to ternary electrolyte systems are given.

Steady stateChemistryInorganic chemistryIonic bondingThermodynamicsFiltration and SeparationElectrolyteBiochemistryMembraneSimple (abstract algebra)Porous membraneGeneral Materials SciencePhysical and Theoretical ChemistryDiffusion (business)Ternary operationJournal of Membrane Science
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