Search results for " solution"

showing 10 items of 3084 documents

Determination of the stoichiometry of mixed microcrystals K x Cs y ZnCl 4 using instrumental neutron activation analysis

1998

Instrumental neutron activation analysis (INAA) has been employed as an absolute method for the determination of the stoichiometry of mixed microcrystals KxCsyZnCl4 with a weight ranging between 20 and 50 μg. The reliability of the method has been checked with the pure substances KCl, NaCl, CsCl and RbCl, for which the mean value of the ratio Cl/X was found to be 1.04 (3).

ChemistryMean valueInorganic chemistryAnalytical chemistryNeutron activation analysisBiochemistryStoichiometrySolid solutionFresenius' Journal of Analytical Chemistry
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Electrochemical Detection of High Oxidation States of Chromium( IV and V ) in Chromium‐Doped Cassiterite and Tin‐Sphene Ceramic Pigmenting Systems

2006

Solid-state electrochemistry is applied to detect the presence of chromium centres with high oxidation states in chromium-doped cassiterite and tin-sphene ceramic pigmenting systems. Voltammetric data indicate that CrV and CrIV centres with different coordinative arrangements exist in the studied materials, and yield proton-assisted reduction processes at +0.95, +0.42 AgCl/Ag in contact with 0.50 M H2SO4. Electrochemical measurements are correlated with spectroscopic data. The CrIV and CrV metal ions display a significant light-driven electrocatalytic effect on the oxidation of 1,4-dihydrobenzoquinone and Fe(CN)64– ions that involves the formation of surface-confined adducts. (© Wiley-VCH V…

ChemistryMetal ions in aqueous solutionInorganic chemistryDopingCassiteritechemistry.chemical_elementengineering.materialElectrochemistryInorganic ChemistryChromiumvisual_artvisual_art.visual_art_mediumengineeringCeramicTinVoltammetryEuropean Journal of Inorganic Chemistry
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Selective CO2 adsorption by a triazacyclononane-bridged microporous metal-organic framework.

2011

Metal-organic frameworks constructed by self-assembly of metal ions and organic linkers have recently been of great interest in the preparation of porous hybrid materials with a wide variety of functions. Despite much research in this area and the large choice of building blocks used to fine-tune pore size and structure, it remains a challenge to synthesise frameworks composed of polyamines to tailor the porosity and adsorption properties for CO(2). Herein, we describe a rigid and microporous three-dimensional metal-organic framework with the formula [Zn(2)(L)(H(2)O)]Cl (L=1,4,7-tris(4-carboxybenzyl)-1,4,7-triazacyclononane) synthesised in a one-pot solvothermal reaction between zinc ions a…

ChemistryMetal ions in aqueous solutionOrganic ChemistryInorganic chemistrySorptionGeneral ChemistryMicroporous materialCatalysisAdsorptionChemical engineeringMetal-organic frameworkGas separationHybrid materialSelectivityChemistry (Weinheim an der Bergstrasse, Germany)
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Preparation and characterization of organofunctionalized bentonite clay bearing aminophosphonic groups in heavy metal uptake

2019

Abstract Bentonite (Bnt) with covalently immobilized N-propylaminodi(methylenephosphonic) groups (Bnt-ADPA) was obtained through a two-step synthesis including aminosilanization and phosphorylation of resulting aminobentonite through Moedritzer-Irani reaction. The grafting of an aminosilane layer in the interplanar space of the bentonite was investigated by XRD, and the presence of N and P-containing groups was confirmed by FTIR, 31P and 29Si MAS NMR. The immobilization of the organic functional groups increased the interplanar distance in bentonite matrix at 52% that essentially improved filtration properties compared to raw bentonite. The number of surface acid groups was evaluated to 0.8…

ChemistryProcess Chemistry and TechnologyMetal ions in aqueous solution02 engineering and technology010501 environmental sciences021001 nanoscience & nanotechnologyGrafting01 natural sciencesPollutionMatrix (chemical analysis)MetalAdsorptionCovalent bondvisual_artBentonitevisual_art.visual_art_mediumChemical Engineering (miscellaneous)Fourier transform infrared spectroscopy0210 nano-technologyWaste Management and Disposal0105 earth and related environmental sciencesNuclear chemistryJournal of Environmental Chemical Engineering
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Surface characterisation of metal ions loaded TiO2 photocatalysts: structure–activity relationship

2004

Abstract Transition metal loaded TiO 2 powders were characterised and tested for the photodegradation of some organic acids. Both Lewis and Bronsted surface acid sites were present in the samples containing large amounts of Mo, V and W. The Bronsted sites are associated to the presence of the transition metals as they do not exist in the unloaded support, and in particular to the presence of these metals in high oxidation states. The trend of the pzc values of the various powders matches rather well both with the surface acidity of the samples experimentally determined by NH 3 adsorption and with a scale of acidity/basicity for bulk binary oxides. XPS investigation indicates that only the p…

ChemistryProcess Chemistry and TechnologyMetal ions in aqueous solutionInorganic chemistryCatalysischemistry.chemical_compoundAdsorptionTransition metalPhotocatalysisReactivity (chemistry)Point of zero chargePhotodegradationGeneral Environmental ScienceBenzoic acidApplied Catalysis B: Environmental
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Rietveld Refinement of Tetragonal V4+–ZrO2 Solid Solutions Obtained from Gels by X-ray Powder Diffraction

2002

Abstract The crystal structure of three tetragonal V x Zr 1− x O 2 solid solutions, with x =0.025, 0.05, and 0.075, prepared by heating dried gel precursors at 450°C in air atmosphere, have been determined by Rietveld refinement on the basis of powder X-ray powder diffractometer data. They contain V 4+ cations surrounded by eight oxygens, four at a distance between 2.079 and 2.093 A and another four at longer distances between 2.369 and 2.348 A. The estimation of the crystal average oxygen position from the X-ray lattice parameter of V x Zr 1− x O 2 conform with the relationship proposed by Howard et al. ( J. Am. Ceram. Soc. 81, 241 (1998)).

ChemistryRietveld refinementCrystal structureCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsInorganic ChemistryCrystalTetragonal crystal systemCrystallographyLattice constantPowder DiffractometerMaterials ChemistryCeramics and CompositesPhysical and Theoretical ChemistryPowder diffractionSolid solutionJournal of Solid State Chemistry
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Phase analysis and oxygen strorage capacity of ceria-lanthana-based TWC promoters prepared by sol-gel routes

2002

Ceria–lanthana-based promoters of three-way catalysts are synthesized by two different sol–gel routes, involving nitrate precursors. The oxygen uptake ability of these compounds is measured by O2 chemisorption. The specific surface area is determined by N2 adsorption (BET). X-ray diffraction data are analyzed by Rietveld refinement, demonstrating that lanthanum forms solid solution with CeO2; its total amount in ceria depends on the competitive formation of La–Al mixed oxides and on the synthetic method. The O2 uptake ability is essentially determined by the La content in the ceria–lanthana solid solution, while it is independent on the surface area and on the CeO2 particle size. The O2 upt…

ChemistryRietveld refinementInorganic chemistrychemistry.chemical_elementRietveld refinementTWC catalystCondensed Matter PhysicsHeterogeneous catalysisElectronic Optical and Magnetic MaterialsceriaInorganic ChemistryAdsorptionChemisorptionSpecific surface areaMaterials ChemistryCeramics and CompositesLanthanumsol-gelPhysical and Theoretical ChemistrySolid solutionSol-geloxygen storage capacity
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Strategies to decrease water drainage and nitrate emission from soilless cultures of greenhouse tomato

2010

In the spring-summer season of 2005 and 2006, we explored the influence of three fertigation strategies (A–C) on the water and nitrogen use efficiency of semi-closed rockwool culture of greenhouse tomato conducted using saline water (NaCl concentration of 9.5 mol m−3). The strategies under comparison were the following: (A) crop water uptake was compensated by refilling the mixing tank with nutrient solution at full strength (with the concentrations of macronutrients equal or close to the corresponding mean uptake concentrations as determined in previous studies) and the recirculating nutrient solution was flushed out whenever its electrical conductivity (EC) surpassed 4.5 dS m−1 due to the…

ChemistrySoil ScienceFertigation Hydroponics Nitrate Directive Nitrogen use efficiencyHydroponicsSaline waterRecirculating nutrient solution Solanum lycopersicum Salinity Semi-closed growing systems Water use efficiencychemistry.chemical_compoundAnimal scienceNutrientAgronomyNitrateWastewaterWater-use efficiencyAgronomy and Crop ScienceSurface waterWater useEarth-Surface ProcessesWater Science and TechnologyAgricultural Water Management
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Oxygen K-edge XANES investigation of NicMg1−cO solid solutions

2005

A series of Ni(c)Mg(1-c)O solid solutions are characterized by means of synchrotron radiation X-ray diffraction and X-ray absorption near-edge-structure spectroscopy at oxygen K-edge (532 eV). A dramatic drop of the pre-edge peak intensity is observed in the Ni(c)Mg(1-c)O system upon dilution. It can be attributed to a decrease of 3d(8)(Ni(2+))-2p(O(2-)) mixing upon dilution with magnesium ions due to a decrease of the number of 3d vacancies as nickel ion is replaced by magnesium ion. Similarly, the decrease of the number of 4s and 4p vacancies also leads to a decrease of 4s4p(Ni(2+))-2p(O(2-)) hybridization, and hence a drop of intensities of features B and C. The features E and F are more…

ChemistrySpectrum AnalysisDrop (liquid)Analytical chemistrychemistry.chemical_elementSodium ChlorideOxygenAtomic and Molecular Physics and OpticsXANESAnalytical ChemistryDilutionOxygenSolutionsX-Ray DiffractionK-edgeNickelMagnesiumSpectroscopyInstrumentationMagnesium ionSpectroscopySolid solutionSpectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
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Protonation of 3-aminopyrroles

1987

Abstract The protonation of 3-aminopyrroles has been investigated using H and 13C n.m.r. spectroscopy. The spectral data are compatible with predominant protonation of the amino group with no evidence for protonation of the pyrrole ring.

ChemistryStereochemistryNuclear TheoryOrganic ChemistryProtonationNuclear magnetic resonance spectroscopyRing (chemistry)BiochemistryMedicinal chemistrychemistry.chemical_compoundDrug DiscoveryPhysics::Accelerator PhysicsChemical solutionNuclear ExperimentSpectroscopySpectral dataPyrroleTetrahedron
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