Search results for "Dissolution"

showing 10 items of 333 documents

Electrochemistry of iron oxide pigments (earths) from pictorial microsamples attached to graphite–polyester composite electrodes

2001

The electrochemical response of different iron pigments attached to graphite–polyester composite electrodes is described. Characteristic differential pulse voltammetric profiles were obtained for green earth, iron oxide red, Mars black, ochre yellow, Sienna raw, umber raw and Van Dyke brown. Proton-assisted reductive dissolution processes occur at the three-phase boundary of the substrate electrode–attached solid–electrolyte solution system. Microsamples extracted from polychromed sculptures, canvas paintings, wall paintings, altarpieces and panel paintings from Spain, Ethiopia and Italy from the 12th to the 20th centuries were electrochemically identified in agreement with polarized light …

Polarized light microscopyMaterials scienceComposite numberMetallurgyIron oxideMineralogyElectrochemistryBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryElectrochemistryEnvironmental ChemistryGraphiteUmberDissolutionSpectroscopyMars BlackThe Analyst
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Highly robust and selective system for water pollutants removal: How to transform a traditional photocatalyst into a highly robust and selective syst…

2019

Highly porous monolithic aerogels based on ZnO photocatalyst and syndiotactic polystyrene (s-PS) were obtained by supercritical CO2 treatment of ZnO/s-PS gels. The prepared aerogels were characterized and their photocatalytic activity was evaluated using phenol and toluene as water pollutant models. The s-PS nanoporous crystalline phase, able to absorb pollutant molecules, was proven to be necessary to ensure high photocatalytic efficiency as the aerogel acts not only as a support, but also as pollutant pre-concentrator. The reusability of ZnO/s-PS aerogels is also strong showing no decrease in photocatalytic activity after six consecutive degradation trials. Finally, the aerogel matrix pre…

PollutantNanoporous crystalline phasesMaterials scienceWater pollutants photodegradationNanoporousGeneral Chemical EngineeringAerogelsAerogelArticleSupercritical fluidlcsh:Chemistrychemistry.chemical_compoundlcsh:QD1-999chemistryChemical engineeringPhotocatalyst supportPhotocatalysisZnODegradation (geology)General Materials SciencePolystyreneDissolutionAerogels; Nanoporous crystalline phases; Photocatalyst support; Water pollutants photodegradation; ZnO
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Crosslinked α,β-Polyasparthydrazide Micromatrices for Controlled Release of Anticancer Drugs

1995

The preparation of new hydrogels by the reaction of α,β- polyasparthydrazide and glutaraldehyde is reported. A different crosslinking degree was obtained by varying the ratio crosslinking agent/polymer which influenced the swelling behavior of the gel. 5-Fluorouracil, was incorporated into the matrices during the crosslinking reaction and in vitro release studies were performed in simulated gastric juice (pH 1.1) and pH 7.4 buffer solution. The hydrogels prepared were chemically stable in the dissolution media. The observed data show the potential application of these new matrices for peroral administration of anticancer agents.

Polymers and Plastics0206 medical engineeringBioengineeringmacromolecular substances02 engineering and technologyBiomaterialschemistry.chemical_compoundPolymer chemistryMaterials ChemistrymedicineDissolutionchemistry.chemical_classificationtechnology industry and agriculturePolymerBuffer solution021001 nanoscience & nanotechnology020601 biomedical engineeringControlled releaseIn vitrochemistrySelf-healing hydrogelsGlutaraldehydeSwellingmedicine.symptom0210 nano-technologyNuclear chemistryJournal of Bioactive and Compatible Polymers
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Elucidation of reaction process between solid tricalcium silicate and a lanthanum salt solution in connection with the precipitation pH. Extension to…

1993

Abstract Dissolution of tricalcium silicate is strongly accelerated in a La salt solution and releases the amounts of OH, Ca and silicate ions just required to precipitate all of lanthanum at pH 8. It remained to be proved that (1) La silicate hydrate could form at pH 8, and (2) Ca silicate hydrate could not precipitate simultaneously. The plot of silicate hydrate and hydroxide precipitation pH of La, Ca and other elements (Th, Zr) against the dropped volume of K2SiO3 and KOH solution and some physico-chemical characterization methods bring affirmative answers to these questions and allow the immobilization process of La and other elements in the presence of tricalcium silicate to be better…

Precipitation (chemistry)Inorganic chemistrychemistry.chemical_elementGeneral ChemistryCondensed Matter PhysicsSilicatechemistry.chemical_compoundSalt solutionchemistryScientific methodLanthanumHydroxideGeneral Materials ScienceHydrateDissolutionSolid State Ionics
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Nucleation and Growth of CaCO3 Mediated by the Egg-White Protein Ovalbumin: A Time-Resolved in situ Study Using Small-Angle Neutron Scattering

2008

Mineralization of calcium carbonate in aqueous solutions starting from its initiation was studied by time-resolved small-angle neutron scattering (SANS). SANS revealed that homogeneous crystallization of CaCO 3 involves an initial formation of thin plate-shaped nuclei which subsequently reassemble to 3-dimensional particles, first of fractal and finally of compact structure. The presence of the egg-white protein ovalbumin leads to a different progression of mineralization through several stages; the first step represents amorphous CaCO 3, whereas the other phases are crystalline. The formation and dissolution of the amorphous phase is accompanied by Ca (2+)-mediated unfolding and cross-link…

Protein FoldingOvalbuminProtein ConformationChemistryNeutron diffractionNucleationWaterGeneral ChemistryNeutron scatteringBiochemistrySmall-angle neutron scatteringCatalysisCalcium Carbonatelaw.inventionAmorphous solidCalcium ChlorideNeutron DiffractionCrystallographyColloid and Surface ChemistrylawVateriteScattering Small AngleCrystallizationCrystallizationDissolutionJournal of the American Chemical Society
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Stability of Prussian Blue films on ITO electrodes: effect of different anions

1993

Abstract Transformation of insoluble newly deposited Prussian Blue (PB) into the soluble structure stabilizes the film and allows its total oxidation to Prussian Yellow. The stability of PB films in electrochemical processes in successive potential cycling experiments and under long-term chemical attack by an electrolyte depends not only on the cation that takes part but also on the nature of the anion present. In aqueous media, the sulphate ion clearly destabilizes the crystalline structure whereas the nitrate ion favours stabilization. Initial changes in the voltammograms recorded immediately after the spectroscopic tests have been detected in all media. During the immersion period water …

Prussian blueAqueous solutionChemistryGeneral Chemical EngineeringInorganic chemistryCrystal structureElectrolyteElectrochemistryRedoxAnalytical ChemistryIonchemistry.chemical_compoundPrussian BlueElectrochemistryanionsDissolutionJournal of Electroanalytical Chemistry
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Improvement of the wettability and dissolution of fenofibrate compacts by plasma treatment

2011

Abstract The goal of this study was to investigate the effect of plasma treatment on the wettability and dissolution of fenofibrate compacts. Contact angle measurements and intrinsic dissolution rate studies of untreated and plasma-treated fenofibrate compacts were conducted. The contact angle data clearly show that the wettability of the tablet surface increased with the duration of plasma treatment. Analyses of stability revealed that the surfaces which were plasma-treated for more than 1 min regained some degree of hydrophobicity after storage in air. Since their hydrophobic recovery finally reached the level observed with 1 min plasma-treated fenofibrate compacts it was deduced that per…

Radiation NonionizingMaterials sciencePlasma irradiationFenofibrateChromatographyDrug CompoundingPharmaceutical SciencePlasma treatmentOxygenContact angleFenofibrateSolubilityChemical engineeringWettabilitymedicineWettingSolubilitySaturation (chemistry)Hydrophobic and Hydrophilic InteractionsDissolutionTabletsmedicine.drugInternational Journal of Pharmaceutics
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Nanoscale etching of III-V semiconductors in acidic hydrogen peroxide solution: GaAs and InP, a striking contrast in surface chemistry

2019

In this study of nanoscale etching for state-of-the-art device technology, the importance of surface chemistry, in particular the nature of the surface oxide, is demonstrated for two III-V materials. Striking differences in etching kinetics were found for GaAs and InP in sulphuric and hydrochloric acidic solutions containing hydrogen peroxide. Under similar conditions, etching of GaAs was much faster, while the dependence of the etch rate on pH, and on H2O2 and acid concentrations also differed markedly for the two semiconductors. Surface analysis techniques provided information on the product layer present after etching: strongly non-stoichiometric porous (hydr)oxides on GaAs and a thin st…

Reaction mechanismta221OxideGeneral Physics and Astronomysurface chemistry02 engineering and technologyreaktiomekanismit010402 general chemistry01 natural scienceschemistry.chemical_compoundpuolijohteetEtching (microfabrication)Hydrogen peroxideDissolutionta114nanoelektroniikkabusiness.industryGaAsInPfungitechnology industry and agricultureSurfaces and InterfacesGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter Physicspintakemia0104 chemical sciencesSurfaces Coatings and Filmsreaction mechanismsSemiconductorchemistryChemical engineeringIII-V oxideHydroxidenanoscale etching0210 nano-technologybusinessStoichiometryApplied Surface Science
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Responsabilité du dirigeant et faute séparable des fonctions

2017

International audience; Note sous Cour de cassation (com.), 5 juillet 2017, n° 15-22.707 (F-D), G.

Responsabilité civileFaute séparable des fonctions[SHS.DROIT]Humanities and Social Sciences/LawLiquidateur[SHS.DROIT] Humanities and Social Sciences/LawGérantLiquidationSOCIETE EN GENERALSOCIETE A RESPONSABILITE LIMITEEResponsabilitéFaute d'abstentionDissolution
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Stan techniczny i wykorzystanie zabudowań po klasztorach skasowanych w guberni wołyńskiej w latach 1832–1853 w świetle raportu wołyńskiego gubernator…

2019

W trakcie XIX-wiecznych kasat klasztorów na obszarze cesarstwa rosyjskiego względy ekonomiczne stanowił istotny, może najważniejszy, ale niejedyny czynnik, uwzględniany przy podejmowaniu decyzji o zniesieniu domu zakonnego. Oficjalnie władze rosyjskie głosiły, że cały majątek klasztorny miał być wykorzystany na utrzymanie szkół oraz instytucji opiekuńczych i charytatywnych. W rzeczywistości przejęte ziemskie dobra klasztorne zasiliły skarb publiczny, a mienie z różnych powodów niezbywalne powiększyło majątek, pozostający w dyspozycji władz gubernialnych oraz Cerkwi prawosławnej. Władze długo nie doceniały znaczenia zabudowań poklasztornych. Dla większości z nich nie znaleziono nowego użytko…

RosjaVolyn GovernorateGubernia Wołyńskakatolickie klasztory męskieRussian armycourtsRussiabudynki klasztornerosyjska administracja cywilnaCerkiew prawosławnawojsko rosyjskieRussian civil administrationmonastery buildingsCatholic male monasteriessądyOrthodox Churchdissolution of monasteries in the 19th centurykasaty klasztorne XIX wEcha Przeszłości
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