Search results for "coating"

showing 10 items of 2834 documents

Ionic liquid gels and antioxidant carbon nanotubes: Hybrid soft materials with improved radical scavenging activity

2019

Hypothesis: Performances of materials are frequently affected by the action of radicals that can induce their degradation. To overcome the above issue, natural antioxidants (AOs) can be added during manufacturing. Considering the high instability of AOs, they have been adsorbed on carbon nanomaterials surface. However, the inclusion of functionalized carbon nanomaterials into gel matrix could enhance the antioxidant efficiency and represent an easy way to disperse and handle the active species.Experiments: Carboxypropyl functionalized carbon nanotubes (f-CNT), pure or with physically adsorbed alpha-tocopherol (f-CNT-VE) and quercetin (f-CNT-Q), were incorporated in some ionic liquid gels (I…

AntioxidantRadicalmedicine.medical_treatmentNatural antioxidants02 engineering and technologyCarbon nanotubeIonic liquid010402 general chemistry01 natural sciencesCarbon nanotubelaw.inventionNatural antioxidantBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryAdsorptionRheologylawmedicineThin filmChemistrySettore CHIM/06 - Chimica Organica021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCoating materialChemical engineeringIonic liquidHybrid ionic liquid gelDegradation (geology)0210 nano-technologyJournal of Colloid and Interface Science
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First total synthesis of antiostatin A1, a potent carbazole-based naturally occurring antioxidant.

2009

The first total synthesis of the potent antioxidant antiostatin A1 is reported, where its key features rely on a chemo- and regioselective rhodium-catalysed crossed alkyne cyclotrimerisation reaction applying functionalised ynamides and a palladium-catalysed arylamidation reaction.

Antioxidantmedicine.medical_treatmentCarbazolesAlkyneAntioxidantsCatalysischemistry.chemical_compoundAntiostatin A1Materials ChemistrymedicineOrganic chemistryRhodiumchemistry.chemical_classificationMolecular StructureCarbazoleMetals and AlloysTotal synthesisRegioselectivityStereoisomerismGeneral ChemistryKey featuresSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryCyclizationCeramics and CompositesPalladiumChemical communications (Cambridge, England)
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Sustainable bioactive pectin-based films to improve fruit safety via a circular economy approach.

2023

This work reports on the valorisation of persimmon (Diospyros kaki Thunb.) for the development of food-grade antiviral coatings against major viral foodborne pathogens, human noroviruses (NoVs) and hepatitis A virus (HAV). Initially, the antiviral activity of polyphenol-rich pectin extracts with abundant non-covalent interactions (PPN), pectin extracts enriched with intact pectin-polyphenol ester and O-glycosyl bonds (PPC) and hydro-ethanolic polyphenol-rich extracts (EPE) was compared. Higher viral reductions were found for the pectin extracts rich in polyphenols, mainly in those containing covalent pectin-polyphenol interactions. This specific extract was mixed with commercial citrus pect…

Antiviral coatingsEdible filmsFruitaPersimmonGeneral Chemical EngineeringMicroorganismes patògensGeneral ChemistryPectin-polyphenol complexesControl de qualitatFood Science
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Photoassisted Oxidation of the Recalcitrant Cyanuric Acid Substrate in Aqueous ZnO Suspensions

2007

The photoassisted oxidative transformation of the highly recalcitrant cyanuric acid was examined in the liquid−solid regime at pH 3 and natural pH 7.5 under UV irradiation in oxygen- and ozone-saturated ZnO suspensions using ZnO as a photomediator. Loss of cyanuric acid was assayed by HPLC UV absorption spectroscopy, whereas intermediates and final products were determined by HPLC ion chromatography (IC), by MS techniques using an electrospray ionization mass spectrometer operated in the negative-ion mode, and by FT-IR spectroscopy. Final reaction products were CO2 gas and NO3- ions. The measure of nitrate in solution quantified the degree of mineralization of the substrate; its concentrati…

Aqueous solutionAbsorption spectroscopyElectrospray ionizationInorganic chemistryIon chromatographySubstrate (chemistry)Mass spectrometrySurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundGeneral EnergyAdsorptionchemistryZnO photocatalyst cyanuric acidPhysical and Theoretical ChemistryCyanuric acidThe Journal of Physical Chemistry C
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Converting p-terphenyl into a novel organo-catalyst for LED-driven energy and electron transfer photoreactions in water.

2021

p-Terphenyl is a potent photoredox catalyst under UV-irradiation. Aiming for more sustainable reaction conditions, we added two sulfonate groups to this key structure to achieve water solubility and incorporated an SO2-bridge thereby shifting the absorption spectrum towards the visible. The resulting photocatalyst shows unexpected triplet reactivity in several test reactions.

Aqueous solutionAbsorption spectroscopyMetals and AlloysGeneral ChemistryPhotochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysischemistry.chemical_compoundElectron transferSulfonatechemistryTerphenylMaterials ChemistryCeramics and CompositesPhotocatalysisReactivity (chemistry)Chemical communications (Cambridge, England)
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Influence of temperature on the synthesis of thiol-stabilized CdTe nanoparticles in aqueous solutions

2010

We have investigated the evolution of thiol-capped cadmium telluride nanocrystals prepared in aqueous solutions at low and room temperature followed by heating at 50–100 °C. The UV–visible absorption spectra, as well as transmission electron microscopy, atomic force microscopy, and dynamic light scattering observations made it possible to reveal differences in size and structure originating from different heating temperatures. It was shown that minimization of the nucleation process temperature provided formation of larger nanoparticles than at higher temperatures.

Aqueous solutionAbsorption spectroscopybusiness.industryChemistryNucleationNanoparticleSurfaces and InterfacesCondensed Matter PhysicsLight scatteringCadmium telluride photovoltaicsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCondensed Matter::Materials ScienceOpticsChemical engineeringDynamic light scatteringTransmission electron microscopyMaterials ChemistryElectrical and Electronic Engineeringbusinessphysica status solidi (a)
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H and 19F NMR Investigation on Mixed Hydrocarbon−Fluorocarbon Micelles

2003

1H and 1 9 F NMR measurements on aqueous solutions of sodium perfluorooctanoate (SPFO) and sodium dodecanoate (SD) mixtures are reported. The surfactant concentration ranged from ∼0.3 to 10 times the critical micelle concentration (cmc ≅ 0.03 mol L - 1 ). The cmc of the SD/SPFO/water mixed system obtained from NMR data was in good agreement with that previously obtained by conductivity measurements. Below the cmc, the experimental chemical shift (δ) was independent of the total concentration for both surfactants. Above the cmc, however, the 6 values for 1 9 F varied linearly with concentration, whereas the values for the hydrogenated surfactant deviated from linearity. These observations in…

Aqueous solutionAggregation numberThermodynamics of micellizationAnalytical chemistryFluorine-19 NMRMicelleSurfaces Coatings and Filmschemistry.chemical_compoundMonomerchemistryPulmonary surfactantCritical micelle concentrationMaterials ChemistryPhysical and Theoretical ChemistryThe Journal of Physical Chemistry B
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Thermodynamic Interaction Parameters for the System Water/NMMO Hydrate

2008

Vapor pressures of water were measured for aqueous solutions of N-methyl-morpholine N-oxide (NMMO) at 80, 90 and 100 degrees C. The Flory-Huggins interaction parameters, chi, calculated from these data as a function of phi, the volume fraction of NMMO, are negative at all concentrations; at low phi, they decrease by more than a factor of 2 as T is raised, whereas they remain almost unchanged as phi approaches unity. Accordingly, the heat of mixing is pronouncedly endothermal at low NMMO concentrations but close to athermal at low water content. The composition dependence of chi can be equally well described by the Redlich-Kister equation and by an approach subdividing the mixing process int…

Aqueous solutionChemistryComposition dependenceVolume fractionMaterials ChemistryThermodynamicsPhysical and Theoretical ChemistryEntropy of mixingHydrateWater contentMixing (physics)Surfaces Coatings and FilmsThe Journal of Physical Chemistry B
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Structure Sensitivity of 2-Methyl-3-butyn-2-ol Hydrogenation on Pd: Computational and Experimental Modeling

2014

In the frame of DFT paradigms, the adsorption of 2-methyl-3-butyn-2-ol (MBY) and 2-methyl-3-buten-2-ol (MBE) on a Pd-30 cluster, including both {100} and {111} faces, was studied along with the pathways involved in the hydrogenation, taking place on plane and low coordination (corner/edge) sites of given MBY/Pd-30 and MBE/Pd-30 surface configurations. The calculated energetics, further validated by gas-phase and water-assisted gas-phase MBY and MBE hydrogenation, performed on well-defined size and shape-controlled Pd nanoparticles supported on SiO2, were able to explain the origin of the structure sensitivity and the high selectivity characterizing the title reaction when occurring in aqueo…

Aqueous solutionChemistryHigh selectivitySurfaces Coatings and FilmsElectronic Optical and Magnetic Materials2-methyl-3-butyn-2-olCrystallographyGeneral EnergyAdsorptionComputational chemistryPd nanoparticlesCluster (physics)MoietySensitivity (control systems)Physical and Theoretical ChemistryThe Journal of Physical Chemistry C
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Mass Action Model Applied to the Thermodynamic Properties of Transfer of Nonionic Copolymers from Water to the Aqueous Surfactant Solutions

2003

A thermodynamic model which enables the properties of aqueous copolymer/surfactant mixtures to be fit quantitatively was proposed. Namely, a relationship between the properties of transfer of the unassociated copolymer from water to the aqueous surfactant solutions (DeltaY(t)) and the surfactant concentration was derived. The model was based on the idea that AY, can be expressed in terms of the following contributions: (1) interaction between monomers of copolymer and surfactant, (2) displacement of the monomer-micelle equilibrium induced by the copolymer, (3) formation of the surfactant-copolymer aggregation complex, and (4) formation of the mixed micelles. Such a model was applied to most…

Aqueous solutionChemistryInorganic chemistrySurfaces Coatings and FilmsCondensed Matter::Soft Condensed MatterThermodynamic modelPulmonary surfactantChemical engineeringMaterials ChemistryCopolymerPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAction modelPolyethylene oxides Micelles scattering DLSThe Journal of Physical Chemistry B
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