Search results for "Chemical process"

showing 10 items of 103 documents

Mechanical, Kinetic and Morphological Correlations during the Scale Growth of Niobium and Zirconium Oxides

2001

Oxidation of niobium at 700°C and zirconium at 850°C, in air or oxygen pressures from 20 to I 000 hPa, lead to the formation in one case of a stratified Nb 2 O 5 oxide scale and in the other case a more compact ZrO 2 oxide scale. Analyses of the evolutions of phases, crystalline textures and mechanical stresses during oxidation are determined by X-ray diffraction techniques. Interactions between chemical processes, crystalline building and mechanical processes constitute together the driving force of the reaction and can explain the differences in morphologies of oxide scales.

Chemical processZirconiumMaterials scienceMechanical EngineeringNiobiumOxidechemistry.chemical_elementMineralogyCondensed Matter PhysicsOxygenCorrosionchemistry.chemical_compoundchemistryChemical engineeringMechanics of MaterialsNiobium oxideGeneral Materials ScienceTexture (crystalline)Materials Science Forum
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Coupled petrological-geodynamical modeling of a compositionally heterogeneous mantle plume

2018

Abstract Self-consistent geodynamic modeling that includes melting is challenging as the chemistry of the source rocks continuously changes as a result of melt extraction. Here, we describe a new method to study the interaction between physical and chemical processes in an uprising heterogeneous mantle plume by combining a geodynamic code with a thermodynamic modeling approach for magma generation and evolution. We pre-computed hundreds of phase diagrams, each of them for a different chemical system. After melt is extracted, the phase diagram with the closest bulk rock chemistry to the depleted source rock is updated locally. The petrological evolution of rocks is tracked via evolving chemi…

Chemical processgeographygeography.geographical_feature_category010504 meteorology & atmospheric sciences010502 geochemistry & geophysics01 natural sciencesMantle (geology)Mantle plumePlumeGeophysicsVolcanoSource rockPetrologyGeothermal gradientGeology0105 earth and related environmental sciencesEarth-Surface ProcessesPhase diagramTectonophysics
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Assessment of the Potential Energy Hypersurfaces in Thymine within Multiconfigurational Theory: CASSCF vs. CASPT2

2016

The present study provides new insights into the topography of the potential energy hypersurfaces (PEHs) of the thymine nucleobase in order to rationalize its main ultrafast photochemical decay paths by employing two methodologies based on the complete active space self-consistent field (CASSCF) and the complete active space second-order perturbation theory (CASPT2) methods: (i) CASSCF optimized structures and energies corrected with the CASPT2 method at the CASSCF geometries and (ii) CASPT2 optimized geometries and energies. A direct comparison between these strategies is drawn, yielding qualitatively similar results within a static framework. A number of analyses are performed to assess t…

Chemistry Multidisciplinary2-DIMENSIONAL ELECTRONIC SPECTROSCOPYPharmaceutical Sciencephotostability0305 Organic Chemistry01 natural sciencesLOWEST TRIPLET-STATEAnalytical ChemistryInterpretation (model theory)Molecular dynamicschemistry.chemical_compoundComputational chemistryDrug DiscoveryComplete active spacePerturbation theoryRETINAL CHROMOPHORE MODELComputingMilieux_MISCELLANEOUSAB-INITIOphotochemistry010304 chemical physicsBasis (linear algebra)ChemistryCOUPLED-CLUSTER METHODSPhotochemical ProcessesPotential energy[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryChemistryChemistry (miscellaneous)2ND-ORDER PERTURBATION-THEORYPhysical SciencesANO BASIS-SETSCASSCF/CASPT2Molecular MedicineThermodynamicsLife Sciences & BiomedicineBiochemistry & Molecular BiologyField (physics)INITIO MOLECULAR-DYNAMICSMolecular Dynamics Simulation010402 general chemistryMolecular physicsArticlelcsh:QD241-441lcsh:Organic chemistryCASSCF/CASPT2; photochemistry; DNA; thymine; photostability0103 physical sciencesthyminePhysical and Theoretical ChemistryULTRAFAST INTERNAL-CONVERSIONScience & TechnologyOrganic ChemistryDNAEXCITED-STATE DYNAMICS0104 chemical sciencesThymineModels ChemicalMolecules; Volume 21; Issue 12; Pages: 1666
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Heterogeneous Dinuclear Rhodium(II) Hydroformylation Catalysts—Performance Evaluation and Silsesquioxane-Based Chemical Modeling

2001

Supported, air stable, and reusable hydroformylation catalysts have been prepared by immobilizing dinuclear rhodium(II) complexes bearing ortho-metalated arylphosphane ligands on amorphous silica and mesoporous MCM-41 supports by phosphane tethers. The oligosilsesquioxane model complex of the catalytic site 1 has been prepared analogously and characterized by single-crystal X-ray diffraction analysis.

ChemistryChemical process modelingchemistry.chemical_elementGeneral ChemistryGeneral MedicineHeterogeneous catalysisCatalysisSilsesquioxaneRhodiumCatalysischemistry.chemical_compoundPolymer chemistryOrganic chemistryAmorphous silicaMesoporous materialHydroformylationAngewandte Chemie
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Application of Dopant-Assisted Atmospheric Pressure Photoionisation HPLC–MS Method for the Sensitive Determination of Polycyclic Aromatic Hydrocarbon…

2017

Multiple food research studies have shown that the polycyclic aromatic hydrocarbon (PAHs) are frequently found in processed cocoa products and chocolate. In a present study a method based on dopant-assisted atmospheric pressure photoionisation (DA-APPI) combined with a liquid chromatography/high-resolution mass spectrometer (HPLC-HRMS) for high-sensitivity analysis of four EU marker PAHs in dark chocolate samples was developed and fully validated according to the performance criteria set in EU guidelines. PAHs detection was achieved by HRMS in positive electrospray ionization mode with toluene used as a dopant to enhance the ionization efficiency of non-polar PAHs. The on-column instrument …

ChryseneElectrospray ionizationPolycyclic aromatic hydrocarbonDark chocolateMass spectrometry01 natural sciencesMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundfoodLimit of DetectionChocolatePolycyclic Aromatic HydrocarbonsChromatography High Pressure LiquidFluoranthenechemistry.chemical_classificationAnthraceneChromatography010405 organic chemistry010401 analytical chemistryReproducibility of ResultsGeneral MedicinePhotochemical Processesfood.food0104 chemical scienceschemistryLinear ModelsPyreneJournal of Chromatographic Science
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Photocatalytic coalescence of functionalized gold nanoparticles.

2009

A novel strategy for the synthesis of chromophore-functionalized AuNPs with a narrow size distribution is reported. It consists of increasing the size of preprepared NPs by means of a fast (second scale) and clean (light and an organic photocatalyst) method. The results agree with thiolate ligand liberation from the NP surface promoted by photogenerated radicals. This lets gold cores come together and finally coalesce.

Coalescence (physics)Materials sciencePyrenesLigandNanoparticleMetal NanoparticlesSurfaces and InterfacesChromophoreCondensed Matter PhysicsPhotochemistryPhotochemical ProcessesCatalysisCatalysisBenzophenonesTransition metalColloidal goldElectrochemistryPhotocatalysisGeneral Materials ScienceGoldSpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Hydrogeochemical changes during managed aquifer recharge (MAR) in a salinised coastal aquifer

2021

15 p. - Supplementary data to this article can be found online at https://doi.org/10.1016/j.apgeochem.2020.104866. - The data used to support the findings of this study are available from http://repositori.uji.es/xmlui/handle/10803/620641.

Context (language use)AquiferSoil science010501 environmental sciences010502 geochemistry & geophysics01 natural scienceschemistry.chemical_compoundNitrateManaged aquifer rechargeGeochemistry and PetrologyEnvironmental ChemistrySulfate0105 earth and related environmental sciencesgeographygeography.geographical_feature_categoryBrackish waterGroundwater rechargeMixing ratiosPollutionSpanish mediterranean aquiferchemistryHydrogeochemical processesEnvironmental scienceCarbonateGroundwater
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Photogenotoxicity of folic acid.

2013

Folic acid (FA), also named vitamin B9, is an essential cofactor for the synthesis of DNA bases and other biomolecules after bioactivation by dihydrofolate reductase (DHFR). FA is photoreactive and has been shown to generate DNA modifications when irradiated with UVA (360 nm) in the presence of DNA under cell-free conditions. To investigate the relevance of this reaction for cells and tissues, we irradiated three different cell lines (KB nasopharyngeal carcinoma cells, HaCaT keratinocytes, and a melanoma cell line) in the presence of FA and quantified cytotoxicity and DNA damage generation. The results indicate that FA is phototoxic and photogenotoxic by two different mechanisms. First, ext…

DNA damageCell SurvivalAntineoplastic AgentsBiochemistrychemistry.chemical_compoundFolic AcidPhysiology (medical)Cell Line TumorDihydrofolate reductaseHumansCell ProliferationbiologyDNA synthesisChemistrySuperoxide DismutaseCatalasePhotochemical ProcessesNuclear DNAHaCaTTetrahydrofolate DehydrogenaseMethotrexateBiochemistryDNA glycosylaseCell culturebiology.proteinFolic Acid AntagonistsDrug Screening Assays AntitumorDNADNA DamageFree radical biologymedicine
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DNA binding, nuclease activity, DNA photocleavage and cytotoxic properties of Cu(II) complexes of N-substituted sulfonamides.

2013

Abstract Ternary copper(II) complexes [Cu(NST)2(phen)] (1) and [Cu(NST)2(NH3)2]·H2O (2) [HNST = N-(4,5-dimethylthiazol-2-yl)naphthalene-1-sulfonamide] were prepared and characterized by physico-chemical techniques. Both 1 and 2 were structurally characterized by X-ray crystallography. The crystal structures show the presence of a distorted square planar CuN4 geometry in which the deprotonated sulfonamide, acting as monodentate ligand, binds to the metal ion through the thiazole N atom. Both complexes present intermolecular π–π stacking interactions between phenanthroline rings (compound 1) and between naphthalene rings (compound 2). The interaction of the complexes with CT DNA was studied b…

DenticityStereochemistryCell SurvivalUltraviolet RaysPhenanthrolineRadicalStackingAscorbic AcidNaphthalenesBiochemistryFluorescence spectroscopyInorganic Chemistrychemistry.chemical_compoundInhibitory Concentration 50Coordination ComplexesCell Line TumorAnimalsHumansDNA CleavageThiazoleNucleaseSulfonamidesBinding SitesbiologyCytotoxinsHydroxyl RadicalDNAHydrogen PeroxidePhotochemical ProcessesKineticschemistrybiology.proteinCattleDNACopperPhenanthrolinesJournal of inorganic biochemistry
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Keggin heteropolyacid H3PW12O40 supported on different oxides for catalytic and catalytic photo-assisted propene hydration

2013

Catalytic and catalytic photo-assisted hydration of propene to form 2-propanol in gas–solid regime at atmospheric pressure and 85 1C were carried out by using a heteropolyacid (POM) supported on different oxides. Binary materials were prepared by impregnation of H3PW12O40 on different commercial and home prepared supports (TiO2, SiO2, WO3, ZrO2, ZnO, Al2O3). Some of the composites were active both for catalytic and catalytic photo-assisted reactions. The Keggin type POM was completely and partially degraded, when supported on ZnO and Al2O3, respectively, and these binary solids always resulted as inactive for both catalytic and catalytic photo-assisted reactions. The supported Keggin POM sp…

DiffractionDiffuse reflectance infrared fourier transformAtmospheric pressureSurface PropertiesScanning electron microscopeWaterGeneral Physics and AstronomyOxidesAlkenesPhotochemical ProcessesPhotochemistryCatalysisTungstenCatalysisPropenechemistry.chemical_compoundchemistryPressureSettore CHIM/07 - Fondamenti Chimici Delle Tecnologiesense organsIrradiationKeggin heteropolyacid catalytic propene hydration photo-assisted propene hydrationParticle SizePhysical and Theoretical ChemistryFourier transform infrared spectroscopyPhysical Chemistry Chemical Physics
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