Search results for "surface"

showing 10 items of 9345 documents

Green extraction approach for the recovery of polyphenols from Croatian olive leaves (Olea europea)

2017

Abstract Pressurized liquid extraction (PLE) is shown as an innovative green technology for the effective extraction of the various phytochemicals from food by-products, therefore the aims of this study were to evaluate the application of PLE to engineer green extracts of Croatian olive leaves ( Olea europaea , cv. Oblica) for potential industrial production (functional foods/pharmaceuticals). PLE was conducted under various cycle numbers (1, 2), temperature (60, 80, 100 °C) and static times (5, 10, 15 min). Obtained extracts were characterized in terms of: (i) total polyphenols (TP); (ii) total flavonoids (TF); hydroxycinnamic acids (HCA); and (iv) flavonols (FLA). Response surface methodo…

chemistry.chemical_classificationOblica olive leaves ; Green extraction ; Pressurized liquid extraction ; Total polyphenols ; Flavonoids ; Hydroxycinnamic acidsChromatographybiologyGeneral Chemical EngineeringExtraction (chemistry)04 agricultural and veterinary sciencesbiology.organism_classification040401 food scienceBiochemistry0404 agricultural biotechnologyFlavonolschemistryOleaPolyphenolResponse surface methodologyFood ScienceBiotechnologyFood and Bioproducts Processing
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Enhanced Sieving of C2‐Hydrocarbon from Methane by Fluoro‐Functionalization of In‐MOF with Robust Stability

2021

Developing efficient adsorbent materials is crucial for adsorption and separation to realize the purification of energy source and raw chemicals. Here, we report a novel and robust 3D In-based MOF built up with fluorine-functionalized ligands, QMOF-2F, with improved separation properties of C2-light hydrocarbons over methane at room temperature respect isoreticular non-fluorinated MOF. QMOF-2F shows a remarkable chemical stability in different solvents, including water, and pH (2-12). DFT calculations support the key role of fluorine-functionalization on the improved performance of QMOF-2F.

chemistry.chemical_classificationOrganic ChemistryGeneral ChemistryBiochemistryMethaneImproved performancechemistry.chemical_compoundAdsorptionHydrocarbonchemistryChemical engineeringSurface modificationChemical stabilityMetal-organic frameworkEnergy sourceChemistry – An Asian Journal
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Vibronic structure in triatomic molecules : The hydrocarbon flame bands of the formyl radical (HCO). A theoretical study

1998

A theoretical study of the vibrational structure of the math 2A′ ground and math 2A′ excited states of the formyl radical, HCO, and its deuterated form, DCO, has been performed. The potential energy surfaces have been computed by means of a multiconfigurational perturbative method, CASPT2. The computed geometries and the harmonic and anharmonic frequencies are successfully compared to the available experimental information. The vibrational intensities of the transition math 2A′↔math 2A′ have been computed both for absorption and emission. The results lead to accurate determinations of several structural parameters and some reassignments of the vibrational transitions of the so-called hydroc…

chemistry.chemical_classificationOrganic compounds ; Free radicals ; Potential energy surfaces ; Vibronic states ; Vibrational statesChemistryTriatomic moleculeAnharmonicityGeneral Physics and AstronomyFree radicalsVibronic statesPotential energyUNESCO::FÍSICA::Química físicaHydrocarbonDeuteriumExcited statePotential energy surfacesOrganic compoundsVibrational statesPhysical and Theoretical ChemistryAbsorption (chemistry)Atomic physicsPhysics::Chemical Physics:FÍSICA::Química física [UNESCO]Astrophysics::Galaxy Astrophysics
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Universal Transients in Polymer and Ionic Transition Metal Complex Light-Emitting Electrochemical Cells

2012

Two types of light-emitting electrochemical cells (LECs) are commonly distinguished, the polymer-based LEC (p-LEC) and the ionic transition metal complex-based LEC (iTMC-LEC). Apart from marked differences in the active layer constituents, these LEC types typically show operational time scales that can differ by many orders of magnitude at room temperature. Here, we demonstrate that despite these differences p-LECs and iTMC-LECs show current, light output, and efficacy transients that follow a universal shape. Moreover, we conclude that the turn-on time of both LEC types is dominated by the ion conductivity because the turn-on time exhibits the same activation energy as the ion conductivity…

chemistry.chemical_classificationOrganic solar cellChemistryAnalytical chemistryIonic bonding02 engineering and technologyGeneral ChemistryPolymerConductivityElectroluminescence010402 general chemistry021001 nanoscience & nanotechnology7. Clean energy01 natural sciencesBiochemistryCatalysis0104 chemical sciencesElectrochemical cellIonColloid and Surface ChemistryChemical physicsIonic conductivity0210 nano-technologyJournal of the American Chemical Society
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The synergy between the CsPbBr3 nanoparticle surface and the organic ligand becomes manifest in a demanding carbon–carbon coupling reaction

2020

We demonstrate here the suitability of CsPbBr3nanoparticles as photosensitizers for a demanding photoredox catalytic homo- and cross-coupling of alkyl bromides at room temperature by merely using visible light and an electron donor, thanks to the cooperative action between the nanoparticle surface and organic capping. Fil: Rosa-Pardo, Ignacio. Instituto de Ciencia Molecular; España. Universidad de Valencia; España Fil: Casadevall, Carla. Barcelona Institute Of Science And Technology. Institut Català D'investigació Química.; España Fil: Schmidt, Luciana Carina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigac…

chemistry.chemical_classificationPEROVSKITE CsPbBr3LigandChemistryMetals and AlloysReinforced carbon–carbonNanoparticleElectron donorGeneral ChemistryPhotochemistryCatalysisCoupling reactionSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysis//purl.org/becyt/ford/1 [https]chemistry.chemical_compoundCARBON-CARBON COUPLING//purl.org/becyt/ford/1.4 [https]Materials ChemistryCeramics and CompositesPHOTOREDOXAlkylVisible spectrumChemical Communications
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Structure of bottle brush polymers on surfaces: weak versus strong adsorption.

2011

Large-scale Monte Carlo simulations are presented for a coarse-grained model of cylindrical molecular brushes adsorbed on a flat structureless substrate, varying both the chain length N of the side chains and the backbone chain length N(b). For the case of good solvent conditions, both the cases of weak adsorption (only 10 to 15% of the monomers being bound to the surface) and strong adsorption (~40% of the monomers being bound to the surface, forcing the bottle brush into an almost 2D conformation) are studied. We focus on the scaling of the total linear dimensions of the cylindrical brush with both chain lengths N and N(b), demonstrating a crossover from rod-like behavior (for not very la…

chemistry.chemical_classificationPersistence lengthQuantitative Biology::BiomoleculesChemistryMonte Carlo methodBrushBackbone chainPolymerSurfaces Coatings and Filmslaw.inventionCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundAdsorptionChemical physicslawPolymer chemistryMaterials ChemistrySide chainPhysical and Theoretical ChemistryScalingThe journal of physical chemistry. B
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Temperature triggered self-assembly of polypeptides into multivalent spherical micelles.

2007

We report herein thermally responsive elastin-like polypeptides (ELPs) in a linear AB diblock architecture with an N-terminal peptide ligand that self-assemble into spherical micelles when heated slightly above body temperature. A series of 10 ELP block copolymers (ELP(BC)'s ) with different molecular weights and hydrophilic-to-hydrophobic block ratios were genetically synthesized by recursive directional ligation. The self-assembly of these polymers from unimers into micelles was investigated by light scattering, fluorescence spectroscopy, and cryo-TEM. These ELP(BC)'s undergo two phase transitions as a function of solution temperature: a unimer-to-spherical micelle transition at an interm…

chemistry.chemical_classificationPhase transitionHot TemperatureLightChemistryCryoelectron MicroscopyTemperatureGeneral ChemistryPolymerBiochemistryKrafft temperatureMicelleCatalysisFluorescence spectroscopyArticleElastinCrystallographyColloid and Surface ChemistrySpectrometry FluorescenceCritical micelle concentrationCopolymerScattering RadiationSelf-assemblyPeptidesMicellesJournal of the American Chemical Society
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Detection of phase transitions in thin films with a quartz crystal microbalance

1996

Abstract The quartz crystal microbalance (QCM) is used to determine the phase transition point of thin films by measuring the change in frequency as a function of temperature. To elucidate this relationship, two types of polymers were studied where the bulk phase transitions were known. We investigated a casted thin film of an amphiphilic polyoxazoline and a Langmuir-Blodgett film comprised of fifteen double layers of an amphotropic polyacrylate. The phase transition points of the thin films could be detected by the QCM which were in the same range as for the bulk materials.

chemistry.chemical_classificationPhase transitionMaterials scienceLayer by layerMetals and AlloysAnalytical chemistrySurfaces and InterfacesQuartz crystal microbalancePolymerSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryAmphiphileMaterials ChemistryThin filmThin Solid Films
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Phase behavior and elastic properties of a slightly crosslinked liquid crystalline main-chain polymer

1990

A liquid crystalline main-chain polymer was slightly crosslinked by a reaction withα, ω-difunctionalized oligo-siloxanes. Crosslinking does not disturb the liquid crystalline phases, which are identified by x-ray measurements as smecticB and smecticA phases. Measurements of the elastic properties of the crosslinked sample show rubber-like elasticity, even in the liquid crystalline phases. A difference of 7 K was found between cooling and heating for the smecticA/isotropic transition from DSC and mechanical measurements.

chemistry.chemical_classificationPhase transitionMaterials sciencePolymers and PlasticsIsotropyPolymerShear modulusColloid and Surface ChemistryDifferential scanning calorimetrychemistryChemical engineeringLiquid crystalX-ray crystallographyMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryElasticity (economics)Colloid & Polymer Science
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Structure and phase transitions of a liquid crystalline polymer

1981

The structures, textures as well as thermodynamic properties of a side chain polymer exhibiting a liquid crystalline phase in addition to a partially crystalline state and the isotropic fluid state were investigated. Furthermore the kinetics of phase transitions between these states were analyzed. It was found that the properties of this polymer are intermediate between that of low molecular weight liquid crystals and common polymers. In particular it was observed that the relation between the liquid crystalline texture and the structure is different from that of low molecular weight liquid crystals and that the properties of the crystalline and liquid crystalline state depend strongly on t…

chemistry.chemical_classificationPhase transitionMaterials sciencePolymers and PlasticsKineticsPolymereye diseasesPhysics::Fluid DynamicsCondensed Matter::Soft Condensed MatterCondensed Matter::Materials ScienceCrystallographyColloid and Surface ChemistrychemistryChemical physicsLiquid crystalTacticityPhase (matter)Materials ChemistrySide chainsense organsTexture (crystalline)Physical and Theoretical ChemistryColloid and Polymer Science
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