Search results for "composites"

showing 10 items of 1905 documents

A topological isomer of the Au25(SR)18−nanocluster

2020

Energetically low-lying structural isomers of the much-studied thiolate-protected gold cluster Au25(SR)18− are discovered from extensive (80 ns) molecular dynamics (MD) simulations using the reactive molecular force field ReaxFF and confirmed by density functional theory (DFT). A particularly interesting isomer is found, which is topologically connected to the known crystal structure by a low-barrier collective rotation of the icosahedral Au13 core. The isomerization takes place without breaking of any Au–S bonds. The predicted isomer is essentially iso-energetic with the known Au25(SR)18− structure, but has a distinctly different optical spectrum. It has a significantly larger collision cr…

Gold clusterMaterials scienceIcosahedral symmetryMetals and Alloys02 engineering and technologyGeneral ChemistryCrystal structure010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCatalysis0104 chemical sciences3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyMolecular dynamicsMaterials ChemistryCeramics and CompositesStructural isomerDensity functional theoryReaxFF0210 nano-technologyIsomerizationChemical Communications
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Solubility and microstructural development of TiO2-containing 3Al2O3·2SiO2 and 2Al2O3·SiO2 mullites obtained from single-phase gels

2007

Abstract The interdependence of the titanium oxide amount and the anisotropic growth of mullites prepared from single-phase gels were investigated. Gels with stoichiometries 3(Al2−xTixO3)·2(SiO2) and 2(Al2−xTixO3)·(SiO2), with 0 ≤ x ≤ 0.15 were prepared by the semialkoxide method. Gels and specimens heated at temperatures between 1200 and 1600 °C were characterized by using infrared spectroscopy (IR), X-ray diffraction (XRD) and transmission and field emission scanning electron microscopies (TEM and FESEM). Al2TiO5 as minor impurity was detected in both series of mullites for gel precursor compositions x = 0.10 and x = 0.15, obtained at temperatures between 1200 and 1600 °C. Variations of l…

Grain growthMaterials scienceImpurityScanning electron microscopeMaterials ChemistryCeramics and CompositesAnalytical chemistryMineralogyInfrared spectroscopyMulliteSolubilityStoichiometryTitanium oxideJournal of the European Ceramic Society
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Comparison of analytical methods and AI tools for material characterisation in hot forming

2002

Abstract Hot forming processes probably represent the most ancient of forming operations and what is more they are still today commonly used in modern mechanical industry in order to obtain sound parts, achieving large deformations with a limited required power. Hot metal forming operations are characterised by a large number of physical and thermal phenomena which have to be taken into account in order to model and design the processes themselves. Actually several thermally activated phenomena occur during the forming processes such as recovery, recrystallisation, grain growth, precipitation, allotropic transformations, etc. In this paper the comparison between an analytical method based o…

Grain growthMaterials scienceMetal formingModeling and SimulationThermalMetals and AlloysCeramics and CompositesMechanical engineeringForming processesIndustrial and Manufacturing EngineeringComputer Science ApplicationsEffective equationJournal of Materials Processing Technology
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New approach for synthesis of poly(ethylglyoxylate) using Maghnite-H + , an Algerian proton exchanged montmorillonite clay, as an eco-catalyst

2017

International audience; In this works, we have explored a new method for a green synthesis of poly(ethylglyoxylate) (PEtG). This method consists on using a montmorillonite clay called Maghnite-H+ as an eco-catalyst to replace triethylamine which is toxic. Cationic polymerization experiments are performed in bulk conditions at three temperatures (-40 degrees C, 25 degrees C, 80 degrees C) and in THF solutions at room temperature (25 degrees C). At 25 degrees C, an optimum ratio of 5 wt% of catalyst leads to molar masses up to 22000 g/mol in THF solutions. Polymerizations in bulk conditions lead to slightly lower masses than experiments conducted in THF solutions. However, bulk polymerization…

Green chemistryThermogravimetric analysisMaterials scienceepsilon-caprolactonePolymers and PlasticsBulk polymerizationMaghnite-H+ring-opening polymerization02 engineering and technologyEthylglyoxylate010402 general chemistry7. Clean energy01 natural sciencesalcoholschemistry.chemical_compoundbiodegradable plasticsMaterials Chemistrycationic polymerizationionic polymerizationsThermal stabilityComposite materialsheet silicatespoly(methyl glyoxylate)degradationchemistry.chemical_classificationMolar masscopolymergreen chemistrybis-macromonomersCationic polymerizationbiodegradable polymerGeneral ChemistryPolymer021001 nanoscience & nanotechnology0104 chemical sciences[ CHIM.POLY ] Chemical Sciences/PolymersMontmorillonite[CHIM.POLY]Chemical Sciences/PolymersChemical engineeringchemistryCeramics and Compositeseco-catalyst0210 nano-technology
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Green Composites a base di materie plastiche post-consumo e cariche organiche naturali

2003

Green composites materie plastiche post-consumo cariche organiche naturali
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Closer to nature: an ATP-driven bioinspired catalytic oxidation process

2013

The capability of DNA to acquire enzyme-like properties has led to the emergence of the so-called DNAzyme field; herein, we take a further leap along this nature-inspired road, demonstrating that a template assembled synthetic G-quartet (TASQ) can act as a pre-catalyst for catalytic peroxidase-mimicking oxidation reactions, whatever its nature (guanine or guanosine-based G-quartets), in an ATP-dependent manner, thereby bringing this bioinspired TASQzyme process even closer to nature.

GuanineDeoxyribozymeGuanosineNanotechnology010402 general chemistry01 natural sciencesRedox[ CHIM ] Chemical SciencesCatalysisCatalysischemistry.chemical_compoundAdenosine TriphosphateMaterials Chemistry[CHIM]Chemical SciencesComputingMilieux_MISCELLANEOUS010405 organic chemistryMetals and AlloysDNA CatalyticGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsG-QuadruplexeschemistryCatalytic oxidationScientific methodCeramics and CompositesOxidation-Reduction
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An oxidatively damaged G-quadruplex/hemin DNAzyme.

2020

International audience; Oxidative damage of guanine to 8-oxoguanine triggers a partial and variable loss of G-quadruplex/hemin DNAzyme activity and provides clues to the mechanistic origins of DNAzyme deactivation, which originates from an interplay between decreased G-quadruplex stability, lower hemin affinity and a modification of the nature of hemin binding sites.

GuanineGuanineDeoxyribozyme010402 general chemistryG-quadruplex01 natural sciencesCatalysisOxidative damage03 medical and health scienceschemistry.chemical_compoundMaterials Chemistrypolycyclic compoundsheterocyclic compoundsBinding site[SDV.BBM.BC]Life Sciences [q-bio]/Biochemistry Molecular Biology/Biochemistry [q-bio.BM]030304 developmental biology0303 health sciencesMolecular StructureMetals and AlloysGeneral ChemistryDNA Catalyticequipment and supplies0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsG-QuadruplexeschemistryCeramics and CompositesBiophysicsOxidation-ReductionHeminChemical communications (Cambridge, England)
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Properties of HO2• radicals induced by γ-ray irradiation in silica nanoparticles

2014

Abstract We report an experimental investigation on the effects of γ -ray irradiation in several types of silica nanoparticles previously loaded with O 2 molecules. They differ in specific surface and average diameter. By electron paramagnetic resonance (EPR) measurements we observe the generation of about 10 18 HO 2 • /cm 3 interstitial radicals. These radicals are induced by reaction of interstitial O 2 molecules with radiolytic H atoms, as previously suggested for O 2 -loaded bulk a-SiO 2 samples. However, at variance with respect to bulk materials, our experimental evidences suggest a different generation process of HO 2 • radical. In fact, by a detailed study of samples exposed to D 2 …

HO2•; O2; Fumed silica; Electron paramagnetic resonance spectroscopy; Raman spectroscopyChemistryRadicalAnalytical chemistryNanoparticleO2Condensed Matter PhysicsElectronic Optical and Magnetic Materialslaw.inventionParamagnetismsymbols.namesakelawHO2•RadiolysisRaman spectroscopyMaterials ChemistryCeramics and CompositessymbolsMoleculePhysical chemistryFumed silicaIrradiationElectron paramagnetic resonanceRaman spectroscopyElectron paramagnetic resonance spectroscopy
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The Se … Hal halogen bonding: Co-crystals of selenoureas with fluorinated organohalides

2021

Abstract Synthesis and structural characterization of binary co-crystals 1–4 is reported in the present paper. Selenourea and 1,1-dimethylselenourea were used as selenium-containing halogen bond (XB) acceptors and iodopentafluorobenzene (IPFB), 1,4-diiodotetrafluorobenzene (1,4-DIFB) and 1,4-dibromotetrafluorobenzene (1,4-DBrFB) as XB donors. A comparative analysis of the similar binary co-crystals of selenourea and thiourea with a halogen donor revealed that Se … Hal halogen bonds are up to 13.12% shorter than the sum of vdW radii, while in case of S … Hal halogen bonds this value is 11.4%. Therefore, selenium tends to form stronger bonds with halogens than sulfur does. Comparisons of XB i…

Halogen bondSelenoureachemistry.chemical_element02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesAcceptorSulfur0104 chemical sciencesElectronic Optical and Magnetic MaterialsInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryThioureaHalogenMaterials ChemistryCeramics and CompositesPhysical and Theoretical Chemistry0210 nano-technologySeleniumJournal of Solid State Chemistry
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Halogen bonding—a key step in charge recombination of the dye-sensitized solar cell

2011

The halogen bonding between [Ru(dcbpy)(2)(SCN)(2)] dye and I(2) molecule has been studied. The ruthenium complex forms a stable [Ru(dcbpy)(2)(SCN)(2)]···I(2)·4(CH(3)OH) adduct via S···I interaction between the thiocyanate ligand and the I(2) molecule. The adduct can be seen as a model for one of the key intermediates in the regeneration cycle of the oxidized dye by the I(-)/I(3)(-) electrolyte in dye sensitized solar cells.

Halogen bondThiocyanateLigandMetals and Alloyschemistry.chemical_elementGeneral ChemistryElectrolytePhotochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAdductRutheniumchemistry.chemical_compoundDye-sensitized solar cellchemistryMaterials ChemistryCeramics and CompositesMoleculeta116Chemical Communications
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