Search results for "visual_art"

showing 10 items of 2987 documents

A recipe for the use of rutile in sedimentary provenance analysis

2012

Abstract Rutile has received considerable attention in the last decade as a valuable petrogenetic indicator mineral. Based on both new and previously published data, we carve out advantages and pitfalls regarding TiO 2 -minerals in sedimentary provenance analysis. This results in a recipe for the use of rutile in provenance studies. The main points are: Rutile geochemistry from different grain size fractions does not differ systematically, and hence rutiles should be extracted from the fraction containing the most rutile grains (usually 63–200 μm). Similarly, different magnetic susceptibility of rutile does not systematically imply different trace element composition. Before interpretation …

AnataseProvenanceMineral010504 meteorology & atmospheric sciencesBrookiteStratigraphyMetamorphic rockMineralogyGeology010502 geochemistry & geophysics01 natural sciencesMagnetic susceptibilityGrain sizeRutilevisual_artvisual_art.visual_art_mediumGeology0105 earth and related environmental sciencesSedimentary Geology
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Photocatalytic Selective Oxidation of 5-(Hydroxymethyl)-2-furaldehyde to 2,5-Furandicarbaldehyde in Water by Using Anatase, Rutile, and Brookite TiO2…

2013

5-(Hydroxymethyl)-2-furaldehyde (HMF) was selectively oxidized to 2,5-furandicarbaldehyde (FDC) in; aqueous medium by using home prepared (HP) anatase, rutile, and brookite TiO2 nanoparticles. HP samples were prepared via a sol-gel method by using TiCl4 as the TiO2 precursor. Commercial TiO2 catalysts were also used for, comparison. All samples were characterized by BET specific surface area, XRD, TGA, and SEM, and the reactivity results showed that HP catalysts are predominantly amorphous and give rise to selectivities toward FDC more than twice that of commercial and well crystallized catalysts.

AnataseRenewable Energy Sustainability and the EnvironmentChemistryBrookiteFuraldehydeGeneral Chemical EngineeringInorganic chemistry5-(Hydroxymethyl)-2-furaldehyde Selective oxidation Photocatalytic synthesis TiO2 25-FurandicarbaldehydeGeneral ChemistryCatalysischemistry.chemical_compoundRutilevisual_artSpecific surface areavisual_art.visual_art_mediumPhotocatalysisEnvironmental ChemistryHydroxymethylSettore CHIM/07 - Fondamenti Chimici Delle TecnologieNuclear chemistryACS Sustainable Chemistry & Engineering
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Home-prepared anatase, rutile, and brookite TiO2 for selective photocatalytic oxidation of 4-methoxybenzyl alcohol in water: reactivity and ATR-FTIR …

2009

5th European Meeting on Solar Chemistry and Photocatalysis -- OCT 04-08, 2008 -- Palermo, ITALY

AnataseSettore ING-IND/24 - Principi Di Ingegneria ChimicaAldehydesCatalystsChemistryBrookiteInorganic chemistryAlcoholSelective photooxidation 4-methoxybenzylalcohol TiO2 ATR-FTIRP-anisaldehydeCatalysischemistry.chemical_compoundOrganic-chemistryGreen routeRutilevisual_artvisual_art.visual_art_mediumPhotocatalysisAqueous suspensionReactivity (chemistry)Partial oxidationSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePhysical and Theoretical Chemistry
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Physicochemical characterization of metal hexacyanometallate–TiO2composite materials

2015

The paper describes the synthesis and characterization of novel TiO2–metal hexacyanometallates (MHCMs) composite materials. The starting material, TiO2, was modified by addition of cobalt-hexacyanoferrate (CoHCF) or iron-hexacyanocobaltate (FeHCC) at various concentrations. The resulting composites were characterized as follows: cyclic voltammetry (CV) followed the formation of TiO2–MHCM clusters, TEM micrographs studied their morphology, XAS and XPS data indicated that MHCM bonds to TiO2 through the nitrogen atom of its –CN group and modifies the environment of Ti compared to that of pure anatase. As expected, and confirmed by UV-Vis and XP-valence band data, the electronic properties of T…

AnataseX-ray absorption spectroscopyMorphology (linguistics)ChemistryGeneral Chemical EngineeringGeneral ChemistryCharacterization (materials science)MetalX-ray photoelectron spectroscopyvisual_artvisual_art.visual_art_mediumPhotocatalysisCOMPOSITESTiO2metalhexacanometallateComposite materialCyclic voltammetryPhotocatalysis
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Surface charge fine tuning of reversed-phase/weak anion-exchange type mixed-mode stationary phases for milder elution conditions.

2015

A series of new mixed-mode reversed-phase/weak anion-exchange (RP/WAX) phases have been synthesized by immobilization of N-undecenyl-3-α-aminotropane onto thiol-modified silica gel by thiol-ene click chemistry and subsequent introduction of acidic thiol-endcapping functionalities of different type and surface densities. Click chemistry allowed to adjust a controlled surface concentration of the RP/WAX ligand in such a way that a sufficient quantity of residual thiols remained unmodified which have been capped by thiol click with either 3-butenoic acid or allylsulfonic acid as co-ligands. In another embodiment, performic acid oxidation of N-undecenyl-3-α-aminotropane-derivatized thiol-modifi…

AnionsAcetonitrilesSulfonic acidBiochemistryAnalytical Chemistrychemistry.chemical_compoundEndcappingSulfhydryl Compoundschemistry.chemical_classificationWaxChromatography Reverse-PhaseChromatographyPerformic acidElutionSilica gelHydrophilic interaction chromatographyOrganic ChemistryGeneral MedicineChromatography Ion ExchangeSilicon DioxideMixed-mode chromatographychemistryvisual_artvisual_art.visual_art_mediumSolventsClick ChemistryHydrophobic and Hydrophilic InteractionsTropanesJournal of chromatography. A
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[3.3]Ferrocenophanes with guanidine bridging units as multisignalling receptor molecules for selective recognition of anions, cations, and amino acid…

2007

The synthesis, electrochemical, and optical properties of a new [3.3]ferrocenophane framework in which two ferrocene subunits, with similar electronic environments, are linked through two substituted guanidine moieties, are reported. The receptors 4-7 have been prepared in good yields by the reaction of bis(carbodiimide) 3 with primary amines. This architecture is exceptionally "tunable" because a variety of "legs" may be appended to the basic [3.3]ferrocenophane scaffold to give a wide range of signaling units. These receptors show remarkable ion-sensing properties, due to the presence of a redox active unit (ferrocene), and an amphoteric binding site (guanidine). In this nitrogen-rich str…

AnionsModels MolecularMetallocenesInorganic chemistryCrystallography X-RayRedoxCatalysisMetalchemistry.chemical_compoundMolecular recognitionCationsElectrochemistryMoleculeFerrous CompoundsAmino AcidsGuanidineGuanidineCarbodiimideFluorescent Dyeschemistry.chemical_classificationSpectrum AnalysisOrganic ChemistryGeneral ChemistryAmino acidCrystallographyFerrocenechemistryvisual_artvisual_art.visual_art_mediumChemistry (Weinheim an der Bergstrasse, Germany)
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Synthesis, reactivity, and computational analysis of halophosphines supported by dianionic guanidinate ligands.

2012

The reported chemistry and reactivity of guanidinate supported group 15 elements in the +3 oxidation state, particularly phosphorus, is limited when compared to their ubiquity in supporting metallic elements across the periodic table. We have synthesized a series of chlorophosphines utilizing homo- and heteroleptic (dianionic)guanidinates and have completed a comprehensive study of their reactivity. Most notable is the reluctancy of these four-membered rings to form the corresponding N-heterocyclic phosphenium cations, the tendency to chemically and thermally eliminate carbodiimide, and the scarcely observed ring expansion by insertion of a chloro(imino)phosphine into a P-N bond of the P-N-…

AnionsModels MolecularPhosphinesRing (chemistry)Crystallography X-RayLigandsBiochemistryGuanidinesCatalysisMetalchemistry.chemical_compoundColloid and Surface ChemistryGroup (periodic table)Oxidation statePolymer chemistryOrganic chemistryMoleculeReactivity (chemistry)ta116chemistry.chemical_classificationMolecular StructureChemistryGeneral ChemistryElectron acceptorvisual_artvisual_art.visual_art_mediumQuantum TheoryPhosphineJournal of the American Chemical Society
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Influence of the anions on the structure and magnetic properties of a series of bis(µ-diphexono)-bridged linear trinuclear copper(II) complexes: an e…

2011

The reaction of H(2)L (N,N'-dimethyl-N,N'-bis(2-hydroxy-3-methoxy-5-methylbenzyl)-ethylenediamine) with different copper salts, in methanol and using a H(2)L/Cu = 2 : 3 molar ratio, led to four new bis(μ-diphenoxo)-bridged Cu(3) complexes of general formula [{Cu(S)(μ-L)}(2)Cu(H(2)O)(2n)]X(2) (S = CH(3)OH, n = 1 and X = BF(4)(-) for (1) or ClO(4)(-) for (2); S = Br(3)(-) anion and n = 1 without any X species for (3); S = H(2)O, n = 0 and X = NO(3)(-) for (4)). The use in the same reaction conditions of 4,4'-bipyridine (4,4'-bipy) as connector led to the chain complex [{Cu(μ-4,4'-bipy)(0.5)(μ-L)}(2)Cu(H(2)O)(2n)](ClO(4))(2)·17H(2)O (5). The structure of the centrosymmetric trinuclear unit in …

AnionsSteric effectsChemistryInorganic chemistryMolecular Conformationchemistry.chemical_elementEthylenediamineModels TheoreticalCrystallography X-RayCopperMagnetic susceptibilityInorganic ChemistryMetalMagneticsCrystallographychemistry.chemical_compoundCoordination Complexesvisual_artOctahedral molecular geometryAtomvisual_art.visual_art_mediumAntiferromagnetismta116CopperDalton Transactions
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Determination of non-ionic and anionic surfactants in industrial products by separation on a weak ion-exchanger, derivatization and liquid chromatogr…

2013

Abstract A method for the determination of priority surfactants, including fatty alcohol ethoxylates (FAE), alkylether sulfates (AES) and linear alkylbenzene sulfonates (LAS) is described. The samples were diluted with 50% methanol at pH 4 prior to solid-phase extraction on a weak anionic exchanger (WAX). The AES and LAS surfactant classes were retained, whereas the non-ionic components, including most FAE oligomers were eluted. After washing the WAX cartridge to remove cations, the remaining hydrophobic FAE oligomers were eluted using hot 80% methanol at pH 4 (at ca. 50 °C). These two eluates were combined to constitute the non-ionic fraction. Then, AES and LAS were eluted using 80% MeOH w…

AnionsWaxPhthalic anhydrideChromatographyEsterificationLinear alkylbenzeneElutionOrganic ChemistryExtraction (chemistry)Fatty alcoholGeneral MedicineHydrogen-Ion ConcentrationChromatography Ion ExchangeBiochemistryAnalytical ChemistrySurface-Active Agentschemistry.chemical_compoundchemistryvisual_artvisual_art.visual_art_mediumMethanolDerivatizationChromatography High Pressure LiquidJournal of Chromatography A
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Watching adsorption and electron beam induced decomposition on the model system Mo(CO)(6)/Cu(111) by X-ray absorption and photoemission spectroscopies

2013

Abstract An in-depth study of the first steps of electron beam assisted growth of Mo from molybdenum hexacarbonyl on Cu(1 1 1) has been carried out exploiting the complementarity of X-ray photoemission and X-ray absorption spectroscopies. Frank van der Merwe (2D) growth mode has been observed for the completion of the two first monolayers of adsorbed molecules through a simple physisorption process. Irradiation of the Mo(CO)6 deposit by 1 keV electron beam induces a modification of molybdenum coordination, the average number of C-neighbors decreasing from 6 to 3. Decomposed molecules remain on the surface after annealing at 520 K and organize themselves, the molybdenum atoms moving in Cu(1 …

Annealing (metallurgy)General Physics and Astronomychemistry.chemical_elementSurfaces and InterfacesGeneral ChemistryCondensed Matter PhysicsMolybdenum hexacarbonylSurfaces Coatings and FilmsMetalCrystallographychemistry.chemical_compoundAdsorptionPhysisorptionchemistryMolybdenumvisual_artMonolayerElectron beam processingvisual_art.visual_art_mediumPhysical chemistry
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