Search results for "hydrothermal synthesis"

showing 10 items of 62 documents

Shape-dependency activity of nanostructured CeO2 in the total oxidation of polycyclic aromatic hydrocarbons

2013

11 figures, 2 tables.-- © 2012. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/

NanocubesMaterials scienceCatalytic total oxidationInorganic chemistryNanoparticlePolycyclic aromatic hydrocarbonCatalysischemistry.chemical_compoundsymbols.namesakeCeriaAdsorptionHydrothermal synthesisReactivity (chemistry)General Environmental ScienceNaphthalenechemistry.chemical_classificationNanotubesVOCProcess Chemistry and TechnologyMorphological diagramNanostructureschemistrysymbolsNanorodsNanorodRaman spectroscopyNaphthaleneApplied Catalysis B: Environmental
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Crystallisation of H3BTC, H3TPO or H2SDA with MII (M = Co, Mn or Zn) and 2,2′-bipyridyl: design and control of co-ordination architecture, and magnet…

1999

The hydrothermal reaction of benzene-1,3,5-tricarboxylic acid (H3BTC) with MII (M = Mn, Co or Zn), tris(4-carboxyphenyl)phosphine oxide (H3TPO) or cis-stilbene-4,4′-dicarboxylic acid (H2SDA) with CoII and 2,2′-bipyridyl (BIPY) gave 1-D co-ordination networks formulated as: [M(HBTC)(BIPY)(H2O)] (M = Mn 1, Co 2, or Zn 3; [Co3(BTC)2(BIPY)2(H2O)6]·4H2O 4, [Co3(TPO)2(BIPY)2(H2O)6]·xH2O 5 and [Co(SDA)(BIPY)(H2O)] 6. Structures 1 and 2 consist of double stranded chains of alternating HBTC dianions and dimeric units MII–MII linked by two µ-(1,1) bridging carboxylates. Magnetic properties of 1 and 2 indicate the presence of ferromagnetic exchange interactions within the dimers. Structures 4 and 5 co…

Phosphine oxidechemistry.chemical_classificationChemistryInorganic chemistryInfrared spectroscopychemistry.chemical_elementGeneral ChemistryCrystal structureTricarboxylic acidchemistry.chemical_compoundDicarboxylic acidPolymer chemistryHydrothermal synthesisMetal-organic frameworkCobaltJournal of the Chemical Society, Dalton Transactions
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Selective propane oxidation over MoVSbO catalysts. On the preparation, characterization and catalytic behavior of M1 phase

2009

Nb-free (SbO)(2)M(20)O(56) catalysts (M = Mo, V) presenting pure M1 phase have been prepared by a post-synthesis treatment with hydrogen peroxide of a heat-treated MoVSbO mixed metal oxide catalyst previously prepared by hydrothermal method. The characterization of catalysts and their results for propane oxidation suggest that the optimization in the preparation of the M1 phase depends strongly on the washing procedure. The optimal removing of Sb species formed during post-synthesis treatment can explain the improvement in the catalytic activity; while the better selectivity to acrylic acid of the catalysts obtained by post-synthesis treatment can be explained by the elimination of M2 phase…

Post-synthesis treatmentInorganic chemistryOxideHeterogeneous catalysisCatalysisCatalysischemistry.chemical_compoundchemistryPropanePhase (matter)Hydrothermal synthesisHydrothermal synthesisPhysical and Theoretical ChemistryM1 phaseSelectivityHydrogen peroxidePropane oxidationMo–V–Sb mixed oxides
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Hydrothermal Synthesis of ZnO Crystals from Zn(OH)2 Metastable Phases at Room to Supercritical Conditions

2014

The originality of this work is to highlight the effect of temperature and pressure on the size and morphology of hydrothermal ZnO particles from ambient to supercritical conditions (T > 374 °C and P > 221 bar) using a unique continuous one-step process. Experiments were carried out from zinc nitrate (Zn(NO3)2) and potassium hydroxide (KOH) solutions in the ranges of 1–300 bar and 30–400 °C. The as-prepared particles of ZnO (flower, ellipsoid, and sphere) and e-Zn(OH)2 (polyhedral) sized from nano to micrometers were characterized by X-ray diffraction and electronic microscopy. The wulfingite phase (e-Zn(OH)2) was detected inside some powders especially at room temperature for higher pressu…

Potassium hydroxideMaterials scienceRietveld refinementAnalytical chemistryMineralogyGeneral ChemistryCondensed Matter PhysicsHydrothermal circulationSupercritical fluidchemistry.chemical_compoundchemistryZinc nitratePhase (matter)Hydrothermal synthesisGeneral Materials ScienceBar (unit)Crystal Growth & Design
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Synthesis of Nanoferroics

2013

The Chapter covers the technological aspects of many chemical and physico-chemical nanofabrication methods relevant to making nanoferroic materials and composites. First, the classification of relevant synthesis methods of nanoferroics has been presented. Synthesis of particular nanoferroics with different chemical bonding like metallic, oxide and non-oxide compounds is considered in details. Among the methods, the mechanochemical, sonochemical, hydrothermal, co-precipitation, emulsion, thermal decomposition of unstable precursors have been analyzed. The competition between new phase nucleation and nuclei growth has been revealed to be controlled using feedback between reaction rate and tem…

Reaction ratechemistry.chemical_compoundMaterials sciencechemistryChemical engineeringEconomies of agglomerationPhase (matter)Thermal decompositionOxideNucleationHydrothermal synthesisNanoparticle
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Mo-W-containing tetragonal tungsten bronzes through isomorphic substitution of molybdenum by tungsten

2010

Mixed metal oxides based in Mo(W)–Nb–V–Te with tetragonal tungsten bronze (TTB) structure have been synthesized by a hydrothermal method from aqueous solutions of the corresponding Keggin-type heteropolyacids and further heat-treatment in N2 at 700 ◦ C. The materials have been characterized by several physico-chemical techniques, i.e. XRD, Raman, FTIR, SEM-EDS, and TEM. This procedure allows controlling the chemical species to be distributed in the different interstices of the TTB skeleton, which is a key factor to regulate the catalytic properties of the final solid. In this sense, the isomorphic replacement of Mo by W results in lattice parameter and crystal morphology variation, although…

Stereochemistrychemistry.chemical_elementGeneral ChemistryTTB-bronzePartial oxidation of propeneTungstenCatalysisMo–V–Te–Nb–W–P–O mixed metal oxidesTetragonal crystal systemCrystallographyLattice constantchemistryTransition metalIsomorphic substitution of molybdenum by tungstenMolybdenumPINTURAX-ray crystallographyHydrothermal synthesisHydrothermal synthesisPartial oxidation
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High-nuclearity Ni-substituted polyoxometalates: a series of poly(polyoxotungstate)s containing 20–22 nickel centers.

2011

Three high-nuclearity Ni-substituted polyoxotungstates (POTs)--[Ni(enMe)2(H2O)2]2[Ni(H2O)6]2[Ni(enMe)2][Ni(H2O)2]1.5[HNi20X4W34(OH)4O136(H2O)6(enMe)8]·11 H2O (3), [Ni(en)2(H2O)]2[H8Ni21X4W34(OH)4O136(en)10(H2O)5]·22 H2O (4), and [Ni(enMe)2]2[H6Ni22X4W34(OH)4O136(H2O)6(enMe)10]·18 H2O (5), in which en = ethylenediamine, enMe = 1,2-diaminopropane, X = 0.5 P+0.5 Ge--were made under hydrothermal conditions and characterized by IR spectroscopy, elemental analysis, thermogravimetric analysis, powder X-ray diffraction, and single-crystal X-ray diffraction. The structures of 3–5 can be viewed as novel derivatives of [H6Ni20P4W34(OH)4O136(enMe)8(H2O)6]·12 H 2O (1) and [Ni(en)2(H2O)]2[H8Ni20P4W34(OH)…

Thermogravimetric analysisMolecular StructureSpectrophotometry InfraredChemistryOrganic ChemistryInorganic chemistryMolecular Conformationchemistry.chemical_elementInfrared spectroscopyEthylenediamineGeneral ChemistryTungsten CompoundsCrystallography X-RayCatalysisNickelchemistry.chemical_compoundCrystallographyNickelPolyoxometalateHydrothermal synthesisMoleculeStructural unitChemistry (Weinheim an der Bergstrasse, Germany)
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Hydrothermal Synthesis of Ionic Liquid [Bmim]OH-Modified TiO2 Nanoparticles with Enhanced Photocatalytic Activity under Visible Light

2010

TiO(2) nanocomposites modified with the ionic liquid [Bmim]OH are synthesized by a hydrothermal procedure. X-ray diffraction, Zeta-potential measurement, TEM, thermogravimetric analysis, photoluminescence, UV/Vis, FTIR, and X-ray photoelectron spectroscopy are used to characterize the TiO(2) nanocomposites. The TiO(2) nanocomposites consist of pure anatase particles of about 10 nm. The modification of [Bmim]OH on the surface of the TiO(2) particles extends the TiO(2) absorption edge to the visible-light region. The electrochemical redox potentials indicated that the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) of [Bmim]OH match well with the valen…

TitaniumAnatasePhotoluminescenceLightPhotoelectron SpectroscopyOrganic ChemistryIonic LiquidsMetal NanoparticlesGeneral ChemistryPhotochemical ProcessesPhotochemistryBiochemistryCatalysischemistry.chemical_compoundUltraviolet visible spectroscopychemistryX-ray photoelectron spectroscopySpectroscopy Fourier Transform InfraredIonic liquidPhotocatalysisHydrothermal synthesisSpectrophotometry UltravioletHOMO/LUMOChemistry - An Asian Journal
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The selective oxidative dehydrogenation of ethane over hydrothermally synthesised MoVTeNb catalysts

2002

Mo–V–Te–Nb metal oxide catalysts prepared by hydrothermal synthesis and heat-treated in N2 at high temperatures (600–700 °C) show high activity and selectivity for the oxidative dehydrogenation of ethane to ethene. Yields of ethene of 75% have been obtained at 400 °C on the best catalysts. Dejoz Garcia, Ana Maria, Ana.M.Dejoz@uv.es

UNESCO::QUÍMICAOxideOxidative phosphorylation:QUÍMICA [UNESCO]CatalysisCatalysisMetalchemistry.chemical_compoundMaterials ChemistryHydrothermal synthesisOrganic chemistryHigh activityHydrothermal synthesisDehydrogenationEthaneCatalystsUNESCO::QUÍMICA::Química inorgánicaChemistryMetals and AlloysGeneral Chemistry:QUÍMICA::Química inorgánica [UNESCO]Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsOxidative dehydrogenation ; Hydrothermal synthesis ; Ethane ; Catalystsvisual_artCeramics and Compositesvisual_art.visual_art_mediumSelectivityOxidative dehydrogenationChem. Commun.
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Syntheses, structures and physical characterization of two new three-dimensional mixed-valence hexadecavanadate derivatives

2007

Abstract Two new hexadecavanadate derivatives, (bpy)[Zn(4,4′-bpy)2]2[H4ClV16O38]·6H2O 1 and (bpy)[Co(4,4′-bpy)2]2[H4ClV16O38]·6H2O 2 (bpy = 4,4′-bipyridine), were synthesized under the hydrothermal conditions and structurally characterized by IR, XPS and EPR spectroscopy, redox titration and single-crystal X-ray diffraction. The two compounds are isostructural and crystallize in the tetragonal non-centrosymmetric space group P-4n2 (No. 118) with a = 17.124(2), b = 17.124(2), c = 14.724(3) A, V = 4317.5(12) A3 and Z = 1 for the compound 1, and a = 17.038(2), b = 17.038(2), c = 14.754(3) A, V = 4282.9(12) A3 and Z = 1 for the compound 2. Compounds 1 and 2 were constructed from 4-connected {H4…

Valence (chemistry)ChemistryOrganic ChemistryAnalytical Chemistrylaw.inventionInorganic ChemistryTetragonal crystal systemCrystallographyOctahedronlawRedox titrationMoleculeHydrothermal synthesisIsostructuralElectron paramagnetic resonanceSpectroscopyJournal of Molecular Structure
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