Search results for "Anhydrous"

showing 10 items of 48 documents

One-Pot Synthesis to Quinone-Based Diaza[3.3]cyclophanes

2017

A simple one-pot synthesis to [3.3]cyclophanes that involves quinone moieties was found. The protocol tolerates a variety of amines that include aliphatic and aromatic structures with different functional groups, such as hydroxy groups, amides, and terminal double and triple bonds. The straightforward synthesis can be performed by a twofold N-alkylation reaction with 2,5-bis(bromomethyl)-3,6-dimethyl-1,4-benzoquinone (1). Neither anhydrous nor inert conditions are required. Various amines can be employed without any activating groups, several functionalities at end groups are tolerated, and the cyclophanes generated can be easily modified or embedded into larger molecular architectures. The…

010405 organic chemistryChemistryOrganic ChemistryOne-pot synthesisfood and beveragesAlkylation010402 general chemistryTriple bond01 natural sciences0104 chemical sciencesQuinonechemistry.chemical_compoundAnhydrousOrganic chemistryAmine gas treatingPhysical and Theoretical ChemistryCyclophaneEuropean Journal of Organic Chemistry
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Lower mantle hydrogen partitioning between periclase and perovskite : a quantum chemical modelling

2016

Abstract Partitioning of hydrogen (often referred to as H2O) between periclase (pe) and perovskite (pvk) at lower mantle conditions (24–80 GPa) was investigated using quantum mechanics, equilibrium reaction thermodynamics and by monitoring two H-incorporation models. One of these (MSWV) was based on replacements provided by Mg2+ ↔ 2H+ and Si4+ ↔ 4H+; while the other (MSWA) relied upon substitutions in 2Mg2+ ↔ Al3+ + H+ and Si4+ ↔ Al3+ + H+. H2O partitioning in these phases was considered in the light of homogeneous (Bulk Silicate Earth; pvk: 75%–pe:16% model contents) and heterogeneous (Layered Mantle; pvk:78%–pe:14% modal contents) mantle geochemical models, which were configured for lower…

010504 meteorology & atmospheric sciencesHydrogenpericlaseAnalytical chemistrySocio-culturalechemistry.chemical_elementengineering.material010502 geochemistry & geophysics01 natural sciencesMantle (geology)chemistry.chemical_compoundGeochemistry and PetrologyOrganic chemistryH2O-partitioningperovskiteEquilibrium constant0105 earth and related environmental sciencesChemistryAb-initio calculationslowermantle; H2O-partitioning; periclase; perovskite.SilicatePartition coefficientlower mantleAnhydrousengineeringPericlaseChemical equilibriumlower mantle H2O-partitioning Ab-initio calculations periclase perovskite
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Role of Water During Crystallization of Amorphous Cobalt Phosphate Nanoparticles

2016

The transformation of amorphous precursors into crystalline solids and the associated mechanisms are still poorly understood. We illuminate the formation and reactivity of an amorphous cobalt phosphate hydrate precursor and the role of water for its crystallization process. Amorphous cobalt phosphate hydrate nanoparticles (ACP) with diameters of ∼20 nm were prepared in the absence of additives from aqueous solutions at low concentrations and with short reaction times. To avoid the kinetically controlled transformation of metastable ACP into crystalline Co3(PO4)2 × 8 H2O (CPO) its separation must be fast. The crystallinity of ACP could be controlled through the temperature during precipitati…

Aqueous solutionChemistryInorganic chemistry02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesAmorphous solidlaw.inventionCrystallinitychemistry.chemical_compoundlawAnhydrousGeneral Materials ScienceCrystallization0210 nano-technologyHydrateThermal analysisCobalt phosphateCrystal Growth & Design
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Anhydrous Amorphous Calcium Oxalate Nanoparticles from Ionic Liquids: Stable Crystallization Intermediates in the Formation of Whewellite

2015

The mechanisms by which amorphous intermediates transform into crystalline materials are not well understood. To test the viability and the limits of the classical crystallization, new model systems for crystallization are needed. With a view to elucidating the formation of an amorphous precursor and its subsequent crystallization, the crystallization of calcium oxalate, a biomineral widely occurring in plants, is investigated. Amorphous calcium oxalate (ACO) precipitated from an aqueous solution is described as a hydrated metastable phase, as often observed during low-temperature inorganic synthesis and biomineralization. In the presence of water, ACO rapidly transforms into hydrated whewe…

Aqueous solutionChemistryWhewelliteOrganic ChemistryCalcium oxalateGeneral Chemistryengineering.materialCatalysislaw.inventionAmorphous solidchemistry.chemical_compoundChemical engineeringlawengineeringAnhydrousWater of crystallizationOrganic chemistryCrystallizationDissolutionChemistry - A European Journal
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A semiempirical correlation between the optical band gap of hydroxides and the electronegativity of their constituents

2000

In analogy with previous results on anhydrous oxides, a correlation is proposed between the optical band gap of hydroxides and the electronegativities of their constituents. Based on the experimental results on passive hydrated layers on metals obtained in our laboratory and the literature data, it is found that the hydroxide band gap varies with the square of the difference between the electronegativities of the metallic cation and the hydroxyl group. Like in the case of anhydrous oxides, two different interpolation lines have been found forsp-metal andd-metal hydroxides, respectively. The proposed correlations predict semiconducting or insulating behavior even for the most electronegative…

Band gapChemistryInorganic chemistryAnalytical chemistryPhotoelectric effectElectroluminescenceElectrochemistryMetalElectronegativitychemistry.chemical_compoundvisual_artElectrochemistryvisual_art.visual_art_mediumAnhydrousHydroxideRussian Journal of Electrochemistry
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Halogen diffusion in a basaltic melt

2007

Abstract The diffusion of the halogens fluorine, chlorine and bromine was measured in a hawaiitic melt from Mt. Etna at 500 MPa and 1.0 GPa, 1250 to 1450 °C at anhydrous conditions; the diffusion of F and Cl in the melt was also studied with about 3 wt% of dissolved water. Experiments were performed using the diffusion-couple technique in a piston cylinder. Most experiments were performed with only one halogen diffusing between the halogen-enriched and halogen-poor halves of the diffusion couple, but a few experiments with a mixture of halogens (F, Cl and Br) were also performed in order to investigate the possibility of interactions between the halogens during diffusion. Fluorine and chlor…

BromineGeochemistry and PetrologyChemistryInorganic chemistryHalogenFluorineAnhydrousChlorinechemistry.chemical_elementDiffusion (business)Thermal diffusivityOrder of magnitudeGeochimica et Cosmochimica Acta
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Mechanochemical Access to Defect-Stabilized Amorphous Calcium Carbonate

2018

Amorphous calcium carbonate (ACC) is an important precursor in the biomineralization of crystalline CaCO3. The lifetime of transient ACC in nature is regulated by an organic matrix, to use it as an intermediate storage buffer or as a permanent structural element. The relevance of ACC in material science is related to our understanding of CaCO3 crystallization pathways. ACC can be obtained by liquid–liquid phase separation, and it is typically stabilized with the help of macromolecules. We have prepared ACC by milling calcite in a planetary ball mill. The ball-milled amorphous calcium carbonate (BM-ACC) was stabilized with small amounts of Na2CO3. The addition of foreign ions in form of Na2C…

CalciteMaterials scienceGeneral Chemical EngineeringRecrystallization (metallurgy)02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesAmorphous calcium carbonate0104 chemical scienceslaw.inventionchemistry.chemical_compoundchemistryChemical engineeringlawMaterials ChemistryAnhydrousCrystallization0210 nano-technologyBall millMacromoleculeBiomineralizationChemistry of Materials
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Formation of the C−S−H Layer during Early Hydration of Tricalcium Silicate Grains with Different Sizes

2005

Portland cement is a mixture of solid phases which all react with water. Tricalcium silicate (Ca3SiO5) is its main component and is often used in model systems to study cement hydration. It is generally recognized that setting and hardening of cement are due to the formation, by a dissolution-precipitation process, of a calcium silicate hydrate (C-S-H) on anhydrous grains during Ca3SiO5 hydration. The purpose of this paper is to study the effect of Ca3SiO5 particle size on the nucleation-growth process of C-S-H. An experimental study of the rate of hydration by using different grain sizes under controlled conditions has been performed. The experimental data have been compared with results o…

CementMaterials scienceMineralogySurfaces Coatings and Filmslaw.inventionchemistry.chemical_compoundPortland cementchemistryChemical engineeringlawMaterials ChemistryHardening (metallurgy)AnhydrousSolid phasesParticle sizePhysical and Theoretical ChemistryCalcium silicate hydrateTricalcium silicateThe Journal of Physical Chemistry B
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Saturated Solutions of Anhydrous Phases in the System Lime-Silica-Water: Example of beta-C2S

1990

Saturated solutions rerely form when the anhydrous constituents of aluminous and portland cement are stirred in water or in lime solutions of increasing concentrations. Apart from monocalcium aluminate, concentration of ions in solution cannot exceed maximum supersaturation with respect to the hydrate most likely to precipitate. The present work shows such a behavior for β-C2S suspended in water and in lime solutions at low concentration. In more concentrated lime solutions, a short lifetime saturation state with respect to β-C2S seems to be reached.

CementSupersaturationMaterials scienceMineralogyengineering.materiallaw.inventionPortland cementchemistry.chemical_compoundChemical engineeringchemistrylawMonocalcium aluminateMaterials ChemistryCeramics and CompositesengineeringAnhydrousHydrateSaturation (chemistry)LimeJournal of the American Ceramic Society
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Synthesis and characterization of the first diorganotin(IV) complexes containing mixed arylazobenzoic acids and having skew trapezoidal bipyramidal g…

2005

Abstract Three diorganotin(IV) complexes of the type, [R 2 Sn(L a H)(L b H)] (R =  n Bu or Me and, L a H and L b H are two different 5-[( E )-2-(aryl)-1-diazenyl]-2-hydroxybenzoate residues; a: aryl = 4′-Cl-(held constant) and b: aryl = 4′-Me or 4′-Br) have been prepared either by reacting n Bu 2 SnO, L a HH′ and L b HH′ (1:1:1) in anhydrous toluene or by reacting Me 2 SnCl 2 , L a HNa and L b HNa (1:1:1) in anhydrous methanol. The products were characterized by microanalysis, IR, NMR ( 1 H, 13 C, 119 Sn) and 119m Sn Mossbauer spectroscopy. A full characterization of the structures of the complexes [ n Bu 2 Sn(L a H)(L b H)] ( 1 and 2 ) and [Me 2 Sn(L a H)(L b H)] ( 3 ) in the solid state w…

ChemistryArylOrganic ChemistryCrystal structureBiochemistryTolueneInorganic ChemistryBipyramidchemistry.chemical_compoundCrystallographyMössbauer spectroscopyMaterials ChemistryAnhydrousMethanolPhysical and Theoretical ChemistrySingle crystal
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