Search results for "electrolyte"

showing 10 items of 746 documents

Direct Analysis of Psilocin and Muscimol in Urine Samples Using Single Drop Microextraction Technique In-Line with Capillary Electrophoresis

2020

The fully automated system of single drop microextraction coupled with capillary electrophoresis (SDME-CE) was developed for in-line preconcentration and determination of muscimol (MUS) and psilocin (PSC) from urine samples. Those two analytes are characteristic active metabolites of Amanita and Psilocybe mushrooms, evoking visual and auditory hallucinations. Study analytes were selectively extracted from the donor phase (urine samples, pH 4) into the organic phase (a drop of octanol layer), and re-extracted to the acidic acceptor (background electrolyte, BGE), consisting of 25 mM phosphate buffer (pH 3). The optimized conditions for the extraction procedure of a 200 &micro

OctanolAnalyteLiquid Phase MicroextractionCalibration curveAmanitacapillary electrophoresisPharmaceutical ScienceElectrolyteUrinesingle drop microextraction01 natural sciencesArticleAnalytical Chemistrylcsh:QD241-44103 medical and health scienceschemistry.chemical_compound0302 clinical medicineCapillary electrophoresislcsh:Organic chemistryLimit of DetectionDrug DiscoverymedicineHumans030216 legal & forensic medicinePhysical and Theoretical ChemistrypsilocinChromatographyChemistrygreen chemistry010401 analytical chemistryOrganic ChemistryElectrophoresis CapillaryHydrogen-Ion ConcentrationmuscimolurinePsilocybin0104 chemical sciencesDilutionChemistry (miscellaneous)PsilocinCalibrationHallucinogensSolventsMolecular MedicinePsilocybemedicine.drugMolecules
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Ion Pairing in the Analysis of Voltammetric Data at the ITIES: RbTPB and RbTPBCl in 1,2-dichloroethane

1995

The association of rubidium-tetraphenylborate (RbTPB) and rubidium-tetrakis(-chlorophenyl)borate (RbTPBCl) ion pairs in the organic solvent 1,2-dichloroethane (DCE) have been obtained from condutivity and voltammetric data. Conductivity measurements given K RbTPBCl =43 100 M -1 and yield a lower bound for K RbTPB (K RbTPB > 70000 M -1 ). The latter association constant is at variance with the previously accepted value. A method for analysing voltammetric data which allows for the determination of the association constants is presented. The positive polarization limit where the transfer of Rb + takes place is shifted by ca. 200 mV when changing the anion of the organic base electrolyte from …

Organic baseChemistryGeneral Chemical EngineeringYield (chemistry)Inorganic chemistryAnalytical chemistrySolvationElectrolyteITIESConductivityEquilibrium constantIon
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On the nature of the forces controlling selectivity in the high performance capillary electrochromatographic separation of peptides

2003

In this minireview, the nature of the forces controlling selectivity in the high performance capillary electrochromatographic (HP-CEC) separation of peptides has been examined. For uncharged and charged peptides, a synergistic interplay occurs in HP-CEC systems between adsorptive/partitioning events and electrokinetically driven motion. Moreover, at high field strengths, both bulk electrophoretic migration and surface electrodiffusion occur. Thus, the migration behavior of peptides in different HP-CEC systems can be rationalized in terms of the combined consequences of these various processes. Moreover, in HP-CEC, the buffer electrolyte interacts with both the peptide analytes and the sorbe…

OsmosisTime FactorsSorbentCapillary actionBiophysicsAnalytical chemistryPeptideContext (language use)ElectrolyteBiochemistryDiffusionBiomaterialsChromatography Micellar Electrokinetic CapillaryIonschemistry.chemical_classificationCapillary electrochromatographyOrganic ChemistryTemperatureElectrophoresis CapillaryGeneral MedicineHydrogen-Ion ConcentrationModels TheoreticalElectrophoresisChemical engineeringchemistrycardiovascular systemPeptidesSelectivityBiopolymers
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Electrode–Electrolyte Compatibility in Solid-Oxide Fuel Cells: Investigation of the LSM–LNC Interface with X-ray Microspectroscopy

2015

Ca:LaNbO4 (LNC) constitutes the last real breakthrough in high-temperature proton conductors, with better chemical and mechanical stability with respect to cerate and zirconate perovskites. However, the low amount of bivalent dopant that can be hosted in the LaNbO4 matrix poses a limit to the proton concentration in the electrolyte. Using synchrotron X-ray microspectroscopy, we investigated the compatibility of annealed LNC/LSM electrolyte/cathode bilayers for proton-conducting SOFCs. The element maps are complemented by microEXAFS and microXANES, giving information on the fate of different cations after diffusion. The X-ray microspectroscopy approach described here is applied for the first…

PROTON CONDUCTORScathodeMaterials scienceGeneral Chemical EngineeringX-ray microspectroscopyXRFOxideelectrolyteElectrolytefuel cellchemistry.chemical_compoundMaterials ChemistrySOFCX-rayCompatibility (geochemistry)General Chemistryelectrodelanthanum manganitelanthanum strontium manganiteEXAFSCHEMICAL COMPATIBILITYchemistryChemical engineeringElectrodemicroXRFFuel cellsLNClanthanum niobateChemistry of Materials
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Suitability of non-glucose-carbohydrates for parenteral nutrition

1975

Postoperative parenteral nutrition can only be optimally effective if the characteristics of post-traumatic metabolism are taken into account. Two main possibilities are discussed for the carbohydrate component of parenteral nutrition during this phase: glucose with high doses of insulin or non-glucose carbohydrates (sugar substitutes) possibly in a suitable combination with glucose. The risks as well as the technical and organisational problems involved in the use of them are discussed and the authors prefer the second of the two alternatives. Possible side effects of non-glucose carbohydrates are pointed out and it is shown how these can be avoided by observing dose guidelines. So far a c…

Parenteral Nutritionmedicine.medical_treatmentBlood sugarPhysiologyFructoseCarbohydrate metabolismCritical Care and Intensive Care MedicineXylitolElectrolyteschemistry.chemical_compoundPregnancyDietary CarbohydratesmedicineHumansSugarXylitolOxalatesAdenine Nucleotidesbusiness.industryInsulinProteinsBilirubinGeneral MedicineMetabolismCarbohydrateLipid MetabolismUric AcidGlucoseParenteral nutritionBiochemistrychemistryLactatesFemaleParenteral Nutrition TotalbusinessEuropean Journal of Intensive Care Medicine
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Influence of temperature and background electrolyte on the sorption of neptunium(V) on Opalinus Clay

2012

Abstract The temperature dependence of the sorption of 8 μM neptunium(V) on Opalinus Clay (OPA, Mont Terri, Switzerland) was investigated between 40 and 80 °C and compared to previous results for 20 °C. The batch experiments were performed under ambient air conditions in synthetic pore water (pH = 7.6, I = 0.4 M) under variation of the solid-to-liquid ratio between 2 and 20 g/L. Under these conditions the sorption of Np(V) on OPA was found to be an endothermic process as the average distribution coefficient (K d ) increases continuously with increasing temperature from 23 ± 4 L/kg at 40 °C to 678 ± 254 L/kg at 80 °C. In the temperature range of 40-80 °C, the plot of log(K d ) vs. 1/T could …

Partition coefficientGeochemistry and PetrologyIonic strengthChemistryMagnesiumNeptuniumEnthalpychemistry.chemical_elementGeologySorptionElectrolyteAtmospheric temperature rangeNuclear chemistryApplied Clay Science
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Passive Transport of Ionic Drugs through Membranes with pH-Dependent Fixed Charges

2001

We have studied both theoretically and experimentally the passive transport of ionic drugs through membranes with pH-dependent fixed charge. The system considered constitutes a simplified model for pH-controlled drug delivery through membranes of biochemical and pharmaceutical interest. The theoretical approach employed is based on the Nernst-Planck flux equations and all of the species present in the system (the neutral or ionic drug and the hydrogen and hydroxide ions) have been taken into account together with a Langmuir-type isotherm for the adsorption of the ionic drug onto the membrane surface. The membrane permeabilities of cationic, anionic, and neutral drugs through porous membrane…

Passive transportChemistryIonic bondingPolyelectrolyteSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryAdsorptionMembraneChemical engineeringPolymer chemistryHydroxideDrug carrierJournal of Colloid and Interface Science
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Regional cerebral blood flow and regional metabolism in cold induced oedema.

1973

24 hours following a cold induced oedema in cats rCBF was measured in the lesion area, the bluish stained cortex immediately adjacent to the lesion, a cortical area remote from the lesion, and in the contralateral uninjured hemisphere. Thereafter the brain was frozen and the respective tissue areas were removed and analyzed for water and electrolyte content as well as metabolite concentrations. It seems, that in the neighbourhood of a local lesion at least 3 different brain regions can be differentiated with regard to their characteristic pattern of data. In non-oedematous regions either hyperaemia or hypoaemia could be observed. In areas with local brain oedema rCBF was reduced inversely p…

Pathologymedicine.medical_specialtyBrain EdemaPhosphocreatineMicrocirculationLesionHyperaemiachemistry.chemical_compoundAdenosine TriphosphateIschemiaCortex (anatomy)medicineAnimalsHypoxiaPyruvatesCerebrospinal FluidDiminutionCATSbusiness.industrySodiumBrainAnatomyWater-Electrolyte BalanceAdenosine MonophosphateAdenosine DiphosphateCold Temperaturemedicine.anatomical_structurechemistryCerebral blood flowRegional Blood FlowInjections IntravenousCatsLactatesPotassiumSurgeryNeurology (clinical)medicine.symptombusinessActa neurochirurgica
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Extracellular space and electrolyte distribution in cortex and white matter of dog brain in cold induced oedema

1973

24 hours after a circumscribed cold injury of the cortex dog brains were perfused from the lateral ventricle and the frontal subarachnoidal space to the cisterna magna with an artificial CSF containing trace amounts of35S-labelled thiosulphate. Simultaneously the extracellular tracer was administered intravenously. Extracellular fluid volume was estimated and found to be increased from 10 to 15% in the oedematous cortex and from 10 to 27% in the oedematous white matter. The actual size of ECS in oedematous white matter, however, must be larger as indicated by the relative alterations of thiosulphate distribution, tissue water, sodium and chloride. Apparently a small part of the fluid accumu…

Pathologymedicine.medical_specialtySodiumThiosulfateschemistry.chemical_elementBrain EdemaCisterna magnaIodine RadioisotopesWhite matterchemistry.chemical_compoundDogsChloridesCortex (anatomy)Sulfur IsotopesExtracellular fluidExtracellularAnimalsMedicineSerum Albumin Radio-IodinatedEvans BlueCerebral CortexStaining and Labelingbusiness.industrySodiumWater-Electrolyte BalanceCold TemperatureDisease Models Animalmedicine.anatomical_structurechemistryBlood-Brain BarrierCerebral cortexPotassiumSurgeryNeurology (clinical)Extracellular SpacebusinessActa Neurochirurgica
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The Electrostatic Expansion of Linear Polyelectrolytes:  Effects of Gegenions, Co-ions, and Hydrophobicity

1997

The molar mass and ionic strength dependence of the dimensions of hydrophobically modified poly(vinylpyridinium) cations are demonstrated to be almost perfectly described by a theoretical expression derived on the basis of only excluded volume considerations. Generally, the effective charge density of the polyions decreases significantly with increasing hydrophobicity and with increasing polarizability of the gegenions. Unexpectedly, the intrinsic excluded volume effect which becomes dominating at high ionic strength not only depends on the hydrophobicity of the polyion but also significantly increases with decreasing polarizability of the gegenions (i.e., if the iodide gegenions are replac…

Persistence lengthchemistry.chemical_classificationMolar massPolymers and PlasticsChemistryOrganic ChemistryEffective nuclear chargePolyelectrolyteInorganic ChemistryIonic strengthPolarizabilityChemical physicsExcluded volumePolymer chemistryMaterials ChemistryCounterionMacromolecules
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