Search results for "aqueous solution"

showing 10 items of 1610 documents

A study of electrochemically-induced corrosion of low carbon steel in a medium modelling acid rain

1994

Complementary electrochemical, spectrophotometric and electron microsopic investigations were made in addition to the conversion electron Mossbauer spectroscopic (CEMS) measurements to learn more about the mechanism of corrosion of low carbon steel samples in aqueous sulfate and sulfite containing sulfate solutions (pH 3.5, 6.5 and 8.5). Passivation of iron in pure sulfate solution was studied in detail in earlier papers. In the present work, we used a solution containing both sulfate and sulfite anions to obtain more information about the effect of acid rain on low carbon steel samples. The compositions and thicknesses of the passive films formed due to the electrochemical treatments were …

Nuclear and High Energy PhysicsAqueous solutionCarbon steelPassivationInorganic chemistryengineering.materialCondensed Matter PhysicsElectrochemistryAtomic and Molecular Physics and OpticsCorrosionchemistry.chemical_compoundSulfitechemistryengineeringPitting corrosionPhysical and Theoretical ChemistrySulfateHyperfine Interactions
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conversion electron Mössbauer study of low carbon steel polarized in aqueous sulfate solution containing sulfite in low concentration

1992

The passivation of low carbon steel was studied in aqueous solution of 0.5 M Na2SO4+0.001 M NaHSO3 at pH=3.5 and 6.5. The found major components at pH-3.5 were: γ-FeOOH and Fe3C, and also FeSO4.H2O could be identified on the surface of the low carbon steel as a minor component. At pH-6.5, the passive film contained only amorphous iron(III)-oxide or oxyhydroxide.

Nuclear and High Energy PhysicsAqueous solutionMaterials sciencePassivationCarbon steelInorganic chemistryElectronengineering.materialCondensed Matter PhysicsAtomic and Molecular Physics and OpticsAmorphous solidchemistry.chemical_compoundSulfitechemistryMössbauer spectroscopyengineeringPhysical and Theoretical ChemistrySulfateHyperfine Interactions
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Electrochemical and conversion electron mössbauer study of corrosion induced by acid rain

1993

Abstract The passivation of low carbon steel was studied in aqueous solution of 0.5M Na2SO4 +0.001M NaHSO3 (pH 3.5, 6.5 and 8.5) which can be considered as a model of acid rain. The used conversion electron Mossbauer spectroscopy (CEMS) with the complementary electrochemical investigations proved that the sulfite ions induce pitting corrosion at pH 3.5 and 6 5 while the measurements showed much weaker pitting at pH 8.5. The compositions and thicknesses of the passive films formed during the electrochemical treatments are determined from the CEM spectra. Only γ-FeOOH was found on the surface of the samples at pH 6.5 and 8.5. Nevertheless, at pH 3.5 the sextet belonging to Fe3C appears in the…

Nuclear and High Energy PhysicsAqueous solutionPassivationCarbon steelChemistryInorganic chemistryengineering.materialElectrochemistryCorrosionchemistry.chemical_compoundSulfiteConversion electron mössbauer spectroscopyPitting corrosionengineeringInstrumentationNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
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Metal ion beams from an ECR ion source using volatile compounds

1994

Abstract A new MIVOC method (Metal Ions from Volatile Compounds) at an ECR ion source gives a means to produce highly charged metal ion beams at room temperature conditions. Chemical compounds containing metallic atoms are utilized. The compound has to fulfill the two basic requirements: Vapour pressure of the compound is relatively high at room temperature. Evaporation and diffusion of the compound into the source take place without dissociation of the molecule. Up to present metal ion beams from iron and nickel compounds have been produced. The maximum currents of 56Fe9+ and 58Ni10+ from natural elements were 23.9 μA and 18.7 μA, respectively. First measurements have demonstrated the abil…

Nuclear and High Energy PhysicsChemistryVapor pressureHigh intensityMetal ions in aqueous solutionInorganic chemistryAnalytical chemistryIon sourceDissociation (chemistry)MetalNickel compoundsvisual_artvisual_art.visual_art_mediumMoleculeInstrumentationNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
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Rapid Radiochemical Separation Procedures from Aqueous Solutions

1992

The state-of-the-art in the field of rapid radiochemical separation procedures is illustrated by two systems using aqueous solutions as input: ARCA, an apparatus for repetitive separations, and SISAK, a centrifuge system for continuous separations. Applications presented are: Solvent extraction of element 105 investigated with 34-s 262105 using ARCA, and decay scheme studies of the fission product 1.0-s 110Tc by means of SISAK.

Nuclear fission productCentrifugeAqueous solutionDecay schemeChromatographyChemistrySolvent extraction
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Stability of parenteral nutrition admixtures containing organic phosphates

1995

The use of organic phosphates to avoid calcium phosphate precipitation in parenteral nutrition mixtures has been proposed. The purpose of this study was to evaluate the stability of total parenteral nutrition admixtures containing glucose-1-phosphate or glycerol phosphate as the phosphate source over 3 days. Three parenteral nutrition admixtures, each containing glucose-1-phosphate (30.0 mmol), glycerol phosphate (31.4 mmol) or inorganic phosphate (30.0 mmol), and their corresponding aqueous phases were prepared in 3-L ethylene vinyl acetate plastic bags and infusion bottles, and stored at 5 +/- 1 degrees C or 22 +/- 3 degrees C without light protection. Physical stability analysis and samp…

Nutrition and DieteticsAqueous solutionChromatographybusiness.industryPrecipitation (chemistry)Ethylene-vinyl acetateCritical Care and Intensive Care MedicinePhosphatechemistry.chemical_compoundCreamingParenteral nutritionBiochemistrychemistryDynamic light scatteringEmulsionMedicinebusinessClinical Nutrition
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Hydrophobicity of ionisable compounds studied by countercurrent chromatography

2011

Countercurrent chromatography (CCC) is a liquid chromatography technique in which the stationary phase is also a liquid. The main chemical process involved in solute separation is partitioning between the two immiscible liquid phases: the mobile phase and the support-free liquid stationary phase. The octanol-water partition coefficients (P(o/w)) is the accepted parameter measuring the hydrophobicity of molecules. It is considered to estimate active principle partitioning over a biomembrane. It was related to the substance biological activity. CCC is able to work with an octanol stationary phase and an aqueous mobile phase. In this configuration, CCC is a useful and easy alternative to measu…

OctanolAdrenergic beta-AntagonistsHydrophobicityAnalytical chemistryIonic bonding01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compoundCountercurrent chromatographyPhase (matter)MoleculeDiureticsCountercurrent DistributionAqueous solutionChromatography010405 organic chemistryHydrophilic interaction chromatography010401 analytical chemistryOrganic ChemistryOctanol–water partition coefficientsGeneral Medicine0104 chemical sciencesPartition coefficientPharmaceutical PreparationschemistryCountercurrent chromatographyIonisable compoundsHydrophobic and Hydrophilic InteractionsJournal of Chromatography A
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Localization of n-alcohols and structural effects in aqueous solutions of sodium dodecyl sulfate

1997

Small-angle neutron Mattering measurements OD sodium dodecyl sulfate aqueous solutions have been performed in the presence of n-alcohols, from methanol to octanol, at different alcohol concentrations. By modeling the experimental intensities, it was possible to obtain structural information and to derive simultaneously the distribution of the alcohols between the aqueous and the micellar phases. It was found that short chain alcohols tend to remain in the aqueous phase and, by altering the solvent properties, induce a decrease in the aggregation number of sodium dodecyl sulfate micelles. On the other hand, alcohols with longer hydrocarbon chains were found to be present in both phases thoug…

OctanolAggregation numberAqueous solutionSurfactantsInorganic chemistryAqueous two-phase systemAlcoholSurfaces and InterfacesCondensed Matter PhysicsMicelleSolventScatteringchemistry.chemical_compoundchemistryElectrochemistryGeneral Materials ScienceSodium dodecyl sulfateAlcoholSodium dodecyl sulfateSpectroscopyMicelleSettore CHIM/02 - Chimica Fisica
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Conservation of optical purity of amino acids: a principal problem in biochemical and proto-biochemical systems.

1981

Dor L-amino acids, regardless of their state (peptide-bound or free, in the solid state or in aqueous solution), tend to racemize. In a living cell this racemization is usually compensated by specific degradation and replacement of the unwanted polypeptides that contain the wrong enantiomers. But a few long-lived proteins that are synthesized at or near birth are never replaced. Well investigated is the racemization of L-aspartic acid at a rate of 0.1 to 1.14 per cent per year in proteins from lenses and dentine. Increased racemization of eye lens proteins has been related to a form of human eye disease known as brunescent cataracts. Also quite well investigated is the racemization of amino…

Optical RotationStereochemistryBiologychemistry.chemical_compoundIsomerismPeptide synthesisOrganic chemistryHumansAmino AcidsEye lensEnantiomeric excessRacemizationEcology Evolution Behavior and SystematicsGeneral Environmental Sciencechemistry.chemical_classificationAspartic AcidAqueous solutionFossilsGeneral MedicineAgricultural and Biological Sciences (miscellaneous)Biological EvolutionAmino acidchemistryPolymerizationSpace and Planetary ScienceDentinGeneral Earth and Planetary SciencesEnantiomerMathematicsOrigins of life
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Low Viscosity of Densely and Highly Polymerized Human Hemoglobin in Aqueous Solution — the Problem Of Stability

1989

In case of chronic and acute tissue oxygen deficit it is of advantage to have an artificial oxygen carrying blood substitute in order to support a least temporarily blood function. From a physico-chemical point of view an artificial oxygen carrying blood substitute must meet 4 main requirements at the desired concentration.

Oxygen-carryingAqueous solutionPolymerizationChemical engineeringChemistryPolymer chemistryTissue oxygenHemoglobinBlood substituteBlood function
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