Search results for "Dissolution"

showing 10 items of 333 documents

Candesartan Cilexetil In Vitro-In Vivo Correlation: Predictive Dissolution as a Development Tool

2020

[EN] The main objective of this investigation was to develop an in vitro-in vivo correlation (IVIVC) for immediate release candesartan cilexetil formulations by designing an in vitro dissolution test to be used as development tool. The IVIVC could be used to reduce failures in future bioequivalence studies. Data from two bioequivalence studies were scaled and combined to obtain the dataset for the IVIVC. Two-step and one-step approaches were used to develop the IVIVC. Experimental solubility and permeability data confirmed candesartan cilexetil. Biopharmaceutic Classification System (BCS) class II candesartan average plasma profiles were deconvoluted by the Loo-Riegelman method to obtain th…

Chromatographygenetic structuresChemistryPharmaceutical Sciencelcsh:RS1-441Time scalingBioequivalenceBCSArticleCandesartan cilexetillcsh:Pharmacy and materia medicaCandesartanIVIVCIn vivomedicinePredictive in vivo-dissolutionIn vitro in vivoSolubilityIVIVCDissolutionmedicine.drugBioequivalence
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Analytical methodologies for chromium speciation in solid matrices: a survey of literature

1998

The analytical literature about chromium speciation in solid samples has been surveyed. From 451 articles published on the speciation of chromium from 1983 to 1997, the methodologies to do speciation in solids after sample pretreatment are discussed, through consideration of the types of samples and their dissolution, the analytical techniques employed for chromium measurement, and the figures of merit of the 86 papers reported in the Analytical Abstracts data base.

Chromium measurementChromiumchemistryGenetic algorithmMetallurgychemistry.chemical_elementMineralogyEnvironmental scienceBiochemistryDissolutionFresenius' Journal of Analytical Chemistry
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Chromium liquid waste inertization in an inorganic alkali activated matrix: Leaching and NMR multinuclear approach

2015

A class of inorganic binders, also known as geopolymers, can be obtained by alkali activation of aluminosilicate powders at room temperature. The process is affected by many parameters (curing time, curing temperature, relative humidity etc.) and leads to a resistant matrix usable for inertization of hazardous waste. In this study an industrial liquid waste containing a high amount of chromium (≈ 2.3 wt%) in the form of metalorganic salts is inertized into a metakaolin based geopolymer matrix. One of the innovative aspects is the exploitation of the water contained in the waste for the geopolymerization process. This avoided any drying treatment, a common step in the management of liquid ha…

ChromiumMagnetic Resonance SpectroscopyEnvironmental EngineeringMaterials scienceHealth Toxicology and MutagenesisIndustrial Wastechemistry.chemical_elementSs MAS NMR geopolymerWaste Disposal FluidInertizationIndustrial wasteChromiumAluminosilicateEnvironmental ChemistryWaste Management and DisposalDissolutionCuring (chemistry)MetakaolinSettore CHIM/02 - Chimica FisicaWaste managementChromium liquid wastePollutionLeaching testHealth Toxicology and MutagenesiGeopolymerchemistryAluminum SilicatesChromium liquid waste Inertization Leaching test ss MAS NMR geopolymersLeaching (metallurgy)Nuclear chemistryJournal of Hazardous Materials
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Electronic properties and corrosion resistance of passive films on austenitic and duplex stainless steels

2018

Abstract Passive films were grown at constant potential in acidic (pH∼2) and alkaline (pH∼13) solutions on chromium, AISI 304L, AISI 316L and Duplex stainless steels. Passive films on chromium grow following a high field mechanism considering the presence of dissolution phenomena. According to the photoelectrochemical characterization, passive films on Cr have a bandgap of 3.4 eV when formed in acidic solution, and of 2.4 eV when formed in alkaline solution due to the formation of Cr(OH)3. These films result to be poorly stable against anodic dissolution due to a very anodic flat band potential. Conversely, impedance and photoelectrochemical measurements proved that passive films on stainle…

ChromiumMaterials sciencePassivationBand gapAustenitic stainless steel020209 energyGeneral Chemical EngineeringPhotoelectrochemistryPassive filmCorrosion resistancechemistry.chemical_element02 engineering and technologyengineering.materialCorrosionChromiumPhotoelectrochemistryMott-Schottky0202 electrical engineering electronic engineering information engineeringElectrochemistryChemical Engineering (all)Austenitic stainless steelDissolutionAustenite021001 nanoscience & nanotechnologySettore ING-IND/23 - Chimica Fisica ApplicatachemistryChemical engineeringengineeringDuplex stainless steel0210 nano-technology
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Electrokinetic capillary chromatography in a polar continuous‐phase water‐in‐oil microemulsion constituted by water, sodium dodecyl sulfate, and n ‐p…

2005

A water-in-oil (w/o) microemulsion (ME) constituted by 15% Tris buffer, pH 8.4, in water and 85% sodium dodecyl sulfate (SDS)/n-pentanol 1:4 mixture, capable of dissolving up to 30% vegetable oils and lard, was used as background electrolyte in reverse microemulsion electrokinetic capillary chromatography (RMEEKC). Owing to the free SDS ions in the continuous phase and some degree of percolation, the ME showed a high conductivity (0.65 mS. cm(-1) at 25 degrees C) and sustained a very stable capillary current. Previous rinsing of the capillary with a quaternary ammonium salt for electroosmotic flow (EOF) reduction, a series of nonionic and anionic solutes dissolved either in the ME or in fat…

Clinical BiochemistryAnalytical chemistrySalt (chemistry)ElectrolyteBiochemistryAnalytical Chemistrychemistry.chemical_compoundElectrokinetic phenomenaPentanolsPlant OilsMicroemulsionAmmoniumSodium dodecyl sulfateDissolutionChromatography Micellar Electrokinetic Capillarychemistry.chemical_classificationAqueous solutionChromatographyElectrophoresis CapillaryReproducibility of ResultsSodium Dodecyl SulfateWaterDietary FatschemistryEmulsionsHydrophobic and Hydrophilic InteractionsELECTROPHORESIS
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Calcification is not the Achilles' heel of cold-water corals in an acidifying ocean

2015

Ocean acidification is thought to be a major threat to coral reefs: laboratory evidence and CO2 seep research has shown adverse effects on many coral species, although a few are resilient. There are concerns that cold-water corals are even more vulnerable as they live in areas where aragonite saturation (?ara) is lower than in the tropics and is falling rapidly due to CO2 emissions. Here, we provide laboratory evidence that net (gross calcification minus dissolution) and gross calcification rates of three common cold-water corals, Caryophyllia smithii, Dendrophyllia cornigera, and Desmophyllum dianthus, are not affected by pCO2 levels expected for 2100 (pCO2 1058 ?atm, ?ara 1.29), and nor a…

CnidariaSettore BIO/07 - EcologiaCaryophyllia smithiiCoralcold-water coralsocean acidificationengineering.materialCaryophyllia smithiiDendrophyllia cornigeraCold-water coralcalcification and dissolutionCalcification PhysiologicAnthozoaTheoryofComputation_ANALYSISOFALGORITHMSANDPROBLEMCOMPLEXITYComputingMethodologies_SYMBOLICANDALGEBRAICMANIPULATIONMediterranean SeaAnimalsEnvironmental ChemistrySeawaterGlobal ChangeReefDesmophyllum dianthuGeneral Environmental ScienceGlobal and Planetary ChangegeographyDesmophyllum dianthusgeography.geographical_feature_categorybiologyEcology2300EcologyAragoniteOcean acidificationfungiCalcification and dissolutionOcean acidificationCoral reefbiochemical phenomena metabolism and nutritionCarbon DioxideHydrogen-Ion Concentrationbiology.organism_classificationAnthozoaOceanographyengineeringCold-water coralsgeographic locationsMathematicsofComputing_DISCRETEMATHEMATICS
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A new view on the kinetics of tricalcium silicate hydration

2016

Abstract C3S hydration is an interesting example of chemical coupling between C3S dissolution, C–S–H and portlandite precipitation. It occurs because Ca2 +, OH− and silicate ions are present in C3S, in both hydration products and in the surrounding solution. Various experimental data sets reveal that the undersaturation with respect to C3S always increases when C3S hydration enters into the deceleratory phase, leading to the conclusion that C3S dissolution is at the origin of this deceleration, not C–S–H growth. In addition, as soon as portlandite precipitates, the dissolution limits the hydration already in the acceleratory hydration step. The evolution of the undersaturation cannot accoun…

Coalescence (physics)Precipitation (chemistry)ChemistryKineticsInorganic chemistry0211 other engineering and technologiesThermodynamics02 engineering and technologyBuilding and Constructionengineering.material021001 nanoscience & nanotechnologyPortlanditeSilicateIonchemistry.chemical_compoundPhase (matter)021105 building & constructionengineeringGeneral Materials Science0210 nano-technologyDissolutionCement and Concrete Research
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Solid-liquid mass transfer coefficients in gas-solid-liquid agitated vessels

1998

The research on mass transfer coefficients in solid-liquid agitated systems has received substantial attention in the past, due both to the interest in fundamental aspects of mass transfer between particles and turbulent fluids and to the importance of practical applications. In contrast, little information is available on solid-liquid mass transfer when a third gaseous phase is also dispersed into the system, in spite of the importance of the applications of gas-solid-liquid agitated systems. In this work a suitable dissolution technique was used to measure the solid-liquid mass transfer coefficient in gas-solid-liquid vessels stirred by either radial or axial impellers. The mechanical pow…

Condensed Matter::Soft Condensed MatterPhysics::Fluid DynamicsMass transfer coefficientWork (thermodynamics)TurbulenceChemistryGeneral Chemical EngineeringPhase (matter)Mass transferThermodynamicsDissipationDissolutionVolumetric flow rate
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Influence Of The Electrical Parameters On The Fabrication Of Copper Nanowires Into Anodic Alumina Templates

2009

Abstract Metallic copper nanowires have been grown into the pores of alumina membranes by electrodeposition from an aqueous solution containing CuSO 4 . and H 3 BO 3 at pH 3. In order to study the influence of the electrical parameters on growth and structure of nanowires, different deposition potentials (both in the region where hydrogen evolution reaction is allowed or not) and voltage perturbation modes (constant potential or unipolar pulsed depositions) were applied. In all cases, pure polycrystalline Cu nanowires were fabricated into template pores, having lengths increasing with the total deposition time. These nanowires were self-standing, because they retain their vertical orientati…

Copper nanowireMaterials scienceAnodic alumina membraneNanowireGeneral Physics and Astronomychemistry.chemical_elementNanotechnologySurfaces and InterfacesGeneral ChemistryCondensed Matter PhysicsCopperGrain sizeSurfaces Coatings and Filmschemistry.chemical_compoundSettore ING-IND/23 - Chimica Fisica ApplicataCopper nanowires; Anodic alumina membranes; Electrodeposition; Self-standing structureschemistryChemical engineeringElectrodepositionAluminium oxideCrystalliteVapor–liquid–solid methodSelf-standing structuresDissolutionDeposition (law)
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Computational stability of an initially radial solution of a growth/dissolution problem in a nonradial implementation

1991

We consider a free boundary problem modelling the growth/dissolution of a crystal. The aim is to investigate the following question: Does the solution to the crystal growth problem posed in two dimensions with radially symmetric initial and boundary condition evolve as a radially symmetric solution?

CrystalMathematical optimizationComputational stabilityChemistryMathematical analysisSymmetric solutionFree boundary problemCrystal growthBoundary value problemDissolution
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