Search results for "Chemical engineering"

showing 10 items of 5892 documents

Understanding the Stability and Recrystallization Behavior of Amorphous Zinc Phosphate

2021

Zinc phosphate, an important pigment in phosphate conversion coatings, forms protective films on rubbing surfaces. We have simulated the underlying reactions under shear by ball-milling zinc phosphate and monitored the reaction of hopeite (Zn3(PO4)2·4H2O) and the retarded recrystallization of the amorphous reaction product by powder X-ray diffraction (PXRD) and quantitative infrared (IR) spectroscopy. Abrasion of stainless steel was simulated by addition of pure 57Fe. The results provide insight into the chemistry of phosphate conversion coatings or during battery cycling of metal phosphates and give theoretical guidance for the preparation of amorphous phosphates. Thermal analysis revealed…

inorganic chemicalsRecrystallization (geology)Materials science02 engineering and technology010402 general chemistry01 natural sciencesMetalchemistry.chemical_compoundImpurityPhysical and Theoretical Chemistrytechnology industry and agricultureZinc phosphate021001 nanoscience & nanotechnologyPhosphate0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAmorphous solidGeneral EnergyChemical engineeringchemistryConversion coatingvisual_artvisual_art.visual_art_medium0210 nano-technologyPowder diffractionThe Journal of Physical Chemistry C
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Nano-sized I12L6 Molecular Capsules Based on the [N⋅⋅⋅I+⋅⋅⋅N] Halogen Bond

2017

Summary Self-assembly of pre-organized subunits with a concave overall shape is an effective strategy for the synthesis of supramolecular capsules. We report the synthesis of a cavitand-based hexameric capsule held together solely by 12 robust [N⋅⋅⋅I + ⋅⋅⋅N] halogen bonds and its characterization in solution and in the gas phase via 1 H NMR spectroscopy, diffusion-ordered nuclear magnetic resonance spectroscopy (DOSY), and electrospray ionization mass spectrometry. The [N⋅⋅⋅I + ⋅⋅⋅N] halogen-bonded hexameric capsule was efficiently synthesized from the isolobal metallosupramolecular Ag + capsule by application of the [N⋅⋅⋅Ag + ⋅⋅⋅N] → [N⋅⋅⋅I + ⋅⋅⋅N] cation-exchange reaction.

inorganic chemicalsStereochemistrycapsuleGeneral Chemical EngineeringElectrospray ionizationSupramolecular chemistrysupramolecular capsule010402 general chemistry01 natural sciencesBiochemistrysupramolecular chemistryresorcinarene cavitandMaterials ChemistryEnvironmental ChemistryHalonium ionhalonium-ion-based nanotechnologyta116silver-to-iodine cation exchangeHalogen bond010405 organic chemistryChemistryBiochemistry (medical)CavitandIsolobal principleself-assemblyGeneral ChemistryNuclear magnetic resonance spectroscopy0104 chemical sciencesCrystallographyhalonium ionProton NMRhalogen bondChem
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Adsorption and desorption surface dynamics of gaseous adsorbate on silicate-1 by molecular dynamics simulation

2013

The dynamics of adsorption and desorption of gaseous molecules on the external surface of a crystal and a membrane of zeolite silicate-1 is investigated by molecular dynamics simulation. The gases ...

inorganic chemicalsSticking coefficientChemistryGeneral Chemical EngineeringAnalytical chemistryGeneral ChemistryCondensed Matter PhysicsSilicaterespiratory tract diseasesQuantitative Biology::Subcellular ProcessesCrystalCondensed Matter::Materials Sciencechemistry.chemical_compoundMolecular dynamicsAdsorptionMembraneChemical physicsModeling and SimulationDesorptionGeneral Materials ScienceAstrophysics::Earth and Planetary AstrophysicsPhysics::Chemical PhysicsZeoliteAstrophysics::Galaxy AstrophysicsInformation SystemsMolecular Simulation
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Novel organo-modifier for thermally-stable polymer-layered silicate nanocomposites

2015

A new novel approach for the stabilisation of polymer-clay nanocomposites has been investigated based on reacting chemically an antioxidant function, a hindered phenol moiety, with an organic modifier based on a quaternary ammonium salt. The chemically linked antioxidant-containing organic modifier (AO-OM) was then introduced into natural montmorillonite (MMt) through a cation-exchange reaction resulting in antioxidant-containing organo-modified clay (AO-OM-MMt). The new antioxidant-containing modified clay, along with other organo-modified clays having a similar organo-modifier but without the reacted antioxidant, were characterised by spectroscopic, thermogravimetric and x-ray diffraction…

inorganic chemicalsThermogravimetric analysisMaterials sciencePolymers and PlasticsPolymer-clay nanocompositeSalt (chemistry)complex mixtureschemistry.chemical_compoundPolymer chemistryMaterials ChemistryMoietyMechanics of MaterialAntioxidant-containing organomodifierchemistry.chemical_classificationMaterials Chemistry2506 Metals and AlloyNanocompositePolymers and PlasticModified montmorillonitePolymerCondensed Matter PhysicsExfoliation jointPA11MontmorilloniteSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryChemical engineeringMechanics of MaterialsDispersion (chemistry)
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Precatalyst or dosing-device? The [Pd2{μ-(C6H4) PPh2}2{μ-O2C(C6H5)}2] complex anchored on a carboxypolystyrene polymer as an effective supplier of pa…

2020

Abstract A new catalyst has been synthesized from the precursor [Pd2{μ-(C6H4) PPh2}2 {μ-O2C(C6H5)}2] immobilized on a carboxypolystyrene polymer that exhibits an excellent dispersion of the Pd (II) centers, reusability, and catalytic activity in front of phenyl bromides. The activity of this new material was studied in detail for the Suzuki-Miyaura reaction and compared to that of Pd nanoparticles (NPs) supported on UVM-7 (a mesoporous silica), and Pd NPs stabilized with polyvinylpirrolydone. The homogeneous/heterogeneous character of the catalytic process was determined from the results of the hot-filtration, centrifugation, poisoning, three phases tests, and from differential sensitivity …

inorganic chemicalschemistry.chemical_classification010405 organic chemistryNanoparticlechemistry.chemical_elementPolymerMesoporous silica010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesCatalysischemistryX-ray photoelectron spectroscopyChemical engineeringCatalytic cycleOxidation statePhysical and Theoretical ChemistryPalladiumJournal of Catalysis
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An unexpected ring carboxylation in the electrocarboxylation of aromatic ketones

2006

The electrocarboxylation of various aromatic ketones, carried out in N-methyl-2-pyrrolidone (NMP) in a diaphragmless cell equipped with a carbon cathode and an aluminium sacrificial anode, yielded, among the products, the target hydroxy acids, the corresponding alcohols and pinacols and, quite surprisingly, detectable amounts of substituted benzoic acids and cycloexene carboxylic acids. These compounds arise from a never reported before electrocarboxylation on the aromatic ring, respectively, for substitution of an aromatic hydrogen and from an addition reaction. For example, the electrocarboxylation of acetophenone gave rise to the substituted benzoic acids in ortho, para and meta position…

inorganic chemicalschemistry.chemical_classificationAddition reactionKetoneorganic chemicalsGeneral Chemical EngineeringReaction intermediateSettore ING-IND/27 - Chimica Industriale E TecnologicaHydrogen atom abstractionchemistry.chemical_compoundMeta-chemistryCarboxylationElectrochemistryOrganic chemistryElectrocarboxylationRing carboxylationKetonesCarbon dioxideUndivided cellsBenzoic acidAcetophenone
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Promoting the activity and selectivity of high surface area Ni–Ce–O mixed oxides by gold deposition for VOC catalytic combustion

2011

Gold supported on nickel cerium oxide catalysts (Ni–Ce–O) have been studied for the total oxidation of propane, as a model for hydrocarbon volatile organic compound emission control. High surface area Ni–Ce–O catalysts were synthesized using a very simple evaporation method, where cerium and nickel salts were evaporated in the presence of a mixture of methanol and oxalic acid. Gold catalysts were prepared following a deposition–precipitation method. A very efficient catalyst for the oxidation of propane, in terms of both activity and selectivity, was obtained. This high activity has been related to the high surface area of the catalyst (and therefore to the presence of more active sites ava…

inorganic chemicalschemistry.chemical_classificationCerium oxideorganic chemicalsGeneral Chemical EngineeringInorganic chemistryOxalic acidchemistry.chemical_elementCatalytic combustionGeneral ChemistryIndustrial and Manufacturing EngineeringCatalysisCeriumchemistry.chemical_compoundNickelHydrocarbonCatalytic oxidationchemistryEnvironmental Chemistryheterocyclic compoundsChemical Engineering Journal
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Electrostatic phenomena in ion exchange membranes

1971

Abstract Specific and transport properties of a cation and an anion exchange membrane in Na + and Cl - form respectively have been measured in water and dioxane water mixtures. A greater electrolyte absorption and a lesser specific conductivity and counterion transport number in solvents at higher dioxane content indicate strong electrostatic interactions between fixed groups in the membrane and counterions.

inorganic chemicalschemistry.chemical_classificationIon exchangeMechanical EngineeringGeneral Chemical EngineeringInorganic chemistryGeneral ChemistryElectrolyteConductivityElectrostaticsMembranechemistryGeneral Materials ScienceIon-exchange membranesCounterionAbsorption (chemistry)Water Science and TechnologyDesalination
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Isobaric Vapor−Liquid Equilibria for Water + Acetic Acid + Potassium Acetate

2004

Isobaric vapor−liquid equilibria for water + acetic acid + potassium acetate at different salt concentrations as well as for solvent + potassium acetate binary mixtures have been obtained at 100 kPa. Potassium acetate is more effective in the salting-out effect (on water) than lithium and sodium acetates. The eNRTL-CT model, which is a combination of electrolyte nonrandom two-liquid and chemical theory models, has been used to fit the experimental data. The binary parameters of the model have been obtained from the experimental binary vapor−liquid equilibria which have been used to suitably reproduce the vapor−liquid equilibria (VLE) for water + acetic acid + potassium acetate ternary syste…

inorganic chemicalschemistry.chemical_classificationTernary numeral systemChromatographyGeneral Chemical EngineeringPotassiumSodiumInorganic chemistrySalt (chemistry)chemistry.chemical_elementGeneral ChemistryElectrolyteSolventAcetic acidchemistry.chemical_compoundchemistryIsobaric processJournal of Chemical & Engineering Data
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ORR Activity and Stability of Co-N/C Catalysts Based on Silicon Carbide Derived Carbon and the Impact of Loading in Acidic Media

2018

This work was supported by the EU through the European Regional Development Fund under projects TK141 “Advanced materials and high-technology devices for energy recuperation systems” (2014-2020.4.01.15-0011), NAMUR ”Nanomaterials - research and applications” (3.2.0304.12-0397) and by the Estonian institutional research grant No. IUT20-13.

inorganic chemicalschemistry.chemical_element02 engineering and technology010402 general chemistryElectrochemistry01 natural sciences7. Clean energyCatalysisElectron transferchemistry.chemical_compoundX-ray photoelectron spectroscopy:NATURAL SCIENCES:Physics [Research Subject Categories]Materials ChemistryElectrochemistrySilicon carbideheterocyclic compoundsRenewable Energy Sustainability and the EnvironmentChemistryorganic chemicals021001 nanoscience & nanotechnologyCondensed Matter PhysicsNitrogen0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemical engineeringDegradation (geology)0210 nano-technologyCarbonJournal of The Electrochemical Society
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