Search results for "QUARTZ"

showing 10 items of 239 documents

Geochronology and Nd-Sr systematics of Lusatian granitoids: significance for the evolution of the Variscan orogen in east-central Europe

1994

A variety of pre-Variscan granitoids and two Variscan monzogranites occurring in the central and western parts of the Lusatian Granodiorite Complex (LGC), Saxonia were dated by the single zircon evaporation method, complemented by whole rock Nd isotopic data and Rb —Sr whole rock and mineral ages. The virtually undeformed pre-Variscan granitoids constitute a genetically related, mostly peraluminous magmatic suite, ranging in composition from two-mica granodiorite, muscovite-bearing biotite quartz diorite (tonalite) and granodiorite to biotite granodiorite and monozogranite.

MineralGeochronologyengineeringGeochemistryengineering.materialPetrologyStructural geologyMineral resource classificationQuartzBiotiteGeologyDioriteZircon
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Retrograde melt-residue interaction and the formation of near-anhydrous leucosomes in migmatites

2010

Considering physical segregation of melt from its residue, the chemical potentials of the components (oxides) are the same in both when segregation occurs. Then, as P–T conditions change, gradients in chemical potential are established between the melt-rich domains and residue permitting diffusional interaction to occur. In particular, on cooling, the chemical potential of H2O becomes higher in the melt segregation than in the residue, particularly when biotite becomes stable in the residue assemblage. Diffusion of water from the melt to the residue promotes crystallization of anhydrous products from the melt and hydrous products in the residue. This diffusive process, when coupled with mel…

MineralogyGeologyengineering.materialMigmatiteGranulitelaw.inventionResidue (chemistry)Chemical engineeringGeochemistry and PetrologylawengineeringAnhydrousPlagioclaseCrystallizationQuartzGeologyBiotiteJournal of Metamorphic Geology
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Iron-clay interactions: Detailed study of the mineralogical transformation of claystone with emphasis on the formation of iron-rich T-O phyllosilicat…

2014

International audience; Iron-minerals-water interactions are of primary importance in the contexts of underground structure engineering (e.g. reactive barriers or deep geological storage) and for the understanding of secondary alteration processes in primitive meteorites. To improve our understanding of these systems, we determine the mineralogical transformations induced by the association of iron and silicates during a cooling through an experimental simulation of iron-clay interactions with a step-by-step procedure in the range of 90 degrees C to 40 degrees C. The run products and solutions are well characterised, by means of different techniques (X-ray diffraction, scanning and transmis…

Mineralogy[SDU.STU]Sciences of the Universe [physics]/Earth Sciences020101 civil engineering02 engineering and technologyengineering.materialGreenalite010502 geochemistry & geophysics01 natural sciences0201 civil engineeringMagnetitechemistry.chemical_compoundGeochemistry and PetrologyKaoliniteDissolutionChloriteQuartz0105 earth and related environmental sciencesMagnetiteIron-claystone interaction; Cronstedtite; Greenalite; Magnetite; Cooling experimentGeologyGreenaliteCronstedtiteIron-claystone interactionCooling experimentMeteoritechemistry13. Climate actionIlliteengineeringGeology
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Elucidation of Carbohydrate Molecular Interaction Mechanism of Recombinant and Native ArtinM

2013

[EN] The quartz crystal microbalance (QCM) technique has been applied for monitoring the biorecognition of ArtinM lectins at low horseradish peroxidase glycoprotein (HRP) concentrations, using a simple kinetic model based on Langmuir isotherm in previous work.(18) The latter approach was consistent with the data at dilute conditions but it fails to explain the small differences existing in the jArtinM and rArtinM due to ligand binding concentration limit. Here we extend this analysis to differentiate sugar-binding event of recombinant (rArtinM) and native (jArtinM) ArtinM lectins beyond dilute conditions. Equivalently, functionalized quartz crystal microbalance with dissipation monitoring (…

Models MolecularPROTEIN ADSORPTIONSURFACEKM+Horseradish peroxidaselaw.inventionsymbols.namesakelawQUARTZ-CRYSTAL MICROBALANCEBINDINGQUIMICA ANALITICAMaterials ChemistryPhysical and Theoretical ChemistrySPECIFICITYGlycoproteinsBinding SitesChromatographybiologyChemistryLectinLangmuir adsorption modelQuartz crystal microbalanceQuartz Crystal Microbalance TechniquesLECTINRecombinant ProteinsSurfaces Coatings and FilmsMannose-Binding LectinsSolvation shellHYDRATION-SHELLQuartz Crystal Microbalance TechniquesBiophysicsbiology.proteinRecombinant DNAsymbolsPlant LectinsBIOMOLECULAR ADSORPTIONARTOCARPINProtein adsorption
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The amorphous silica-liquid water interface studied by ab initio molecular dynamics (AIMD): local organization in global disorder

2014

International audience; The structural organization of water at a model of amorphous silica-liquid water interface is investigated by ab initio molecular dynamics (AIMD) simulations at room temperature. The amorphous surface is constructed with isolated, H-bonded vicinal and geminal silanols. In the absence of water, the silanols have orientations that depend on the local surface topology (i.e. presence of concave and convex zones). However, in the presence of liquid water, only the strong inter-silanol H-bonds are maintained, whereas the weaker ones are replaced by H-bonds formed with interfacial water molecules. All silanols are found to act as H- bond donors to water. The vicinal silanol…

Models MolecularProtonSurface Propertiesamorphous silicawatergeminal silanols02 engineering and technologyMolecular Dynamics Simulation010402 general chemistry01 natural sciencesAb initio molecular dynamicsComputational chemistryMoleculeGeneral Materials ScienceQuartzGeminalMolecular StructureChemistryab initio molecular dynamicsHydrogen Bonding[CHIM.MATE]Chemical Sciences/Material chemistrySilanes021001 nanoscience & nanotechnologyCondensed Matter PhysicsSilicon Dioxide0104 chemical sciencesAmorphous solidChemical physicsQuantum TheoryAmorphous silicaProtons0210 nano-technologyVicinal
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Formation of irreversibly bound annexin A1 protein domains on POPC/POPS solid supported membranes

2008

AbstractThe specific interaction of annexin A1 with phospholipid bilayers is scrutinized by means of scanning force and fluorescence microscopy, quartz crystal microbalance, ellipsometry, and modeled by dynamic Monte Carlo simulations. It was found that POPC/POPS bilayers exhibit phase separation in POPC- and POPS-enriched domains as a function of Ca2+ concentration. Annexin A1 interacts with POPC/POPS bilayers by forming irreversibly bound protein domains with monolayer thickness on POPS-enriched nanodomains, while the attachment of proteins to the POPC-enriched regions is fully reversible. A thorough kinetic analysis of the process reveals that both, the binding constant of annexin A1 at …

Models Moleculargenetic structuresLipid BilayersBiophysicsPhospholipidAnalytical chemistryPhosphatidylserines02 engineering and technologyMicroscopy Atomic ForceBiochemistryBiophysical PhenomenaMembrane Lipids03 medical and health scienceschemistry.chemical_compoundProtein structureSFMMonolayerMicropatterned membranesAnimalsHumansPOPCMonte Carlo simulationAnnexin A1030304 developmental biologyFluorescence microscopy0303 health sciencesEllipsometrytechnology industry and agricultureCell BiologyQuartz crystal microbalanceSurface Plasmon Resonance021001 nanoscience & nanotechnologyBinding constantProtein Structure TertiaryMembraneMicroscopy FluorescencechemistryQCMPhosphatidylcholinesBiophysicsCalciumlipids (amino acids peptides and proteins)Adsorption0210 nano-technologyMonte Carlo MethodProtein BindingAnnexin A1Biochimica et Biophysica Acta (BBA) - Biomembranes
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Solubility of the assemblage albite+K-feldspar+andalusite+quartz in supercritical aqueous chloride solutions at 650 °C and 2 kbar

2003

Abstract The solubility of the high grade pelite assemblage albite+K-feldspar+andalusite+quartz at 650 °C and 2 kbar was determined in aqueous solutions over a total chloride range of 0.01–3 mCltot using rapid-quench hydrothermal technique. The concentration of Na, K, Si, and Al was determined in the fluid phase after quench. The K/Na ratio was determined by approaching the equilibrium from below and above. It is 0.34 at low chloride concentrations and decreases slightly to 0.31 with increasing total chloride. Silica and aluminum concentrations were determined only from undersaturation. The silica solubility is found to be independent of chloride concentration and is ∼0.13 molal. Aluminum i…

MolalityAqueous solutionChemistryAnalytical chemistryMineralogyGeologyengineering.materialChlorideSupercritical fluidAndalusiteAlbiteGeochemistry and PetrologymedicineengineeringSolubilityQuartzmedicine.drugChemical Geology
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Reduction of Polymerization Shrinkage Stress and Marginal Microleakage Using Soft-Start Polymerization

2003

Purpose: This study evaluated the influence of a soft-start light-curing exposure on polymerization shrinkage stress and marginal integrity of adhesive restorations. Materials and Methods: Six resin-based composites (Pertac II, Tetric Ceram, Definite, Surefil, Solitaire, and Visio-Molar) were adhesively bonded to a cylindrical cavity (n = 9 per material/light) in a photoelastic material. Visible light-curing was applied using either the standard polymerization mode (800 mW/cm2 exposure duration 40 s) of the curing light (Elipar TriLight, 3M ESPE) or the exponential mode from the same device (ramp-curing: 150 mW/cm2 to 800 mW/cm2 within the first 15 s of a total curing time of 40 s). Polymer…

MolarTime FactorsMaterials scienceSiloxanesPolymersSurface PropertiesComposite ResinsPhosphatesAcetonePolymethacrylic AcidsHardnessMaterials TestingHumansBisphenol A-Glycidyl MethacrylatePhosphoric AcidsComposite materialDental EnamelGeneral DentistryLightingCuring (chemistry)ShrinkageDental CementumDental LeakageEthanolEnamel paintTerpenesQuartzDental Marginal AdaptationHardnessDental Marginal AdaptationResin CementsPolymerizationDentin-Bonding Agentsvisual_artvisual_art.visual_art_mediumMethacrylatesAdhesiveJournal of Esthetic and Restorative Dentistry
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Enhanced Acid Dissociation at the Solid/Liquid Interface

2019

In this chapter we review some recent results from first principles molecular dynamics simulations which show how molecular properties, such as proton dissociation, can be influenced upon adsorption at a solid/liquid interface. In particular, we discuss in details the increased acidity of pyruvic acid at the quartz /water interface, which is of relevance for the chemistry of the atmosphere. Our simulations unveil the special role of the microsolvation at interface, as well as the role of the silanols in stabliziing the deprotonated form of the acid. The enhanced acidity at the hydrophilic quartz/water interface is at odd with what typically found at the water/air interface where acidity is …

Molecular dynamicsDeprotonationAdsorptionChemical engineeringChemistryInterface (Java)Liquid interfaceQuartzSolid liquidAcid dissociation constant
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The Role of Side-Arms for Supramolecular Affinity Materials Based on 9,9′-Spirobifluorenes

2017

An eightfold functionalized D2d-symmetric 9,9' spirobifluorene was condensed with a collection of diketones with elaborated structural features to form three-dimensional supramolecular architectures with active surfaces. Gas sorption measurements by quartz crystal microbalances revealed remarkable indications about the molecular interactions for the application as affinity materials for the detection of volatile organic compounds. Single-crystal X-ray structure analysis further gave insight by packing motifs and for potential host-guest interactions.

Molecular interactionsStructure analysis010405 organic chemistryChemistryOrganic ChemistrySupramolecular chemistrySorption010402 general chemistry01 natural sciences0104 chemical sciencesCrystalMolecular recognitionComputational chemistryOrganic chemistryPhysical and Theoretical ChemistryQuartzEuropean Journal of Organic Chemistry
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