Search results for "mesoporous"

showing 10 items of 358 documents

Morphology and properties of poly(methyl methacrylate) (PMMA) filled with mesoporous silica (MCM-41) prepared by melt compounding

2016

This paper reports on the morphologies of poly(methyl methacrylate) (PMMA)/mesoporous silica (MCM-41) composites prepared by melt compounding with various MCM-41 contents in the range of 0.1–5 wt%, the interactions between the polymer and filler in these composites, and their thermomechanical, mechanical and thermal degradation properties. The composites formed transparent films at low filler loadings (\0.5 wt%) because of well-dispersed, unagglomerated particles. The presence of polymer did not alter the pore dimensions in the MCM-41 structure and it maintained its hexagonal structure, even though the polymer chains partially penetrated the pores during composite preparation. The PMMA inte…

Materials scienceComposite number02 engineering and technology010402 general chemistry01 natural scienceschemistry.chemical_compoundMCM-41morphologyGeneral Materials ScienceThermal stabilityMechanics of MaterialComposite materialMethyl methacrylateSettore CHIM/02 - Chimica Fisicachemistry.chemical_classificationMechanical EngineeringThermal stabilityPolymerMesoporous silica021001 nanoscience & nanotechnologyPoly(methyl methacrylate)Materials science0104 chemical scienceschemistryMechanics of Materialsvisual_artvisual_art.visual_art_mediumMaterials Science (all)0210 nano-technologyGlass transition
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Temperature dependence of magnetization reversal in Co and Fe3O4 nanowire arrays

2005

Abstract In this paper, we investigate the magnetization reversal of cobalt and magnetite nanowires, 4 nm in diameter, synthesized within the pores of mesoporous silica thin films. A SQUID magnetometer was used to study the magnetic properties of the nanowire arrays over a broad temperature interval, T= 1.8–300 K. The magnetization reversal process was found to be strongly temperature dependent. While a coherent rotation may occur at room temperature, a process involving the formation of domain structures takes place as the temperature decreases down to 1.8 K.

Materials scienceCondensed matter physicsMagnetometerNanowirechemistry.chemical_elementMesoporous silicaCondensed Matter PhysicsElectronic Optical and Magnetic Materialslaw.inventionchemistry.chemical_compoundTransition metalchemistrylawThin filmPorous mediumCobaltMagnetiteJournal of Magnetism and Magnetic Materials
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Optimization of MCM-41 type silica nanoparticles for biological applications: Control of size and absence of aggregation and cell cytotoxicity

2015

Abstract Mesoporous silica nanoparticles were synthesized at high pH using CTAB as a template and TEOS as a silica precursor. It was shown that varying the NaOH concentration between 5 and 27.5 mM allows the size, pore and silica structure of mesoporous nanoparticles to be precisely tuned. In particular, monodisperse nanoparticles with the MCM-41 structure with size ranging from 90 nm to 450 nm were obtained by increasing the NaOH concentration from 12.5 to 22.5 mM. It thus demonstrates that NaOH concentration must range between 12.5 and 15 mM in order to prepare MCM-41 silica nanoparticles with optimal size for nanovectorization. We also found that under usual conditions the aggregation of…

Materials scienceDispersityExtraction (chemistry)NanoparticleMesoporous silicaCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsSuspension (chemistry)symbols.namesakeChemical engineeringMCM-41Materials ChemistryCeramics and CompositessymbolsOrganic chemistryRaman spectroscopyMesoporous materialJournal of Non-Crystalline Solids
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Enhanced manganese content in Mn-MCM-41 mesoporous silicas

2005

The use of triethanolamine containing complexes of Si and Mn as hydrolytic precursors allows the synthesis of doped mesoporous silicas in which the Mn content can be modulated up to reach a minimum value of the Si/Mn molar ratio of 3. This limit value corresponds to a Mn relative content significantly higher than those reported to date for similar materials (Si/Mn = 6). According to XRD, TEM and porosity data, the mesoporous nature typical of the MCM-41 silicas is retained even for the samples having the highest Mn content.

Materials scienceDopingGeneral Physics and Astronomychemistry.chemical_elementMineralogyManganeseHydrolysisTransition metalMCM-41chemistryTriethanolaminemedicinePorosityMesoporous materialmedicine.drugNuclear chemistryJournal de Physique IV (Proceedings)
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Effects of Pressure, Thermal Treatment, and O2 Loading in MCM41, MSU-H, and MSU-F Mesoporous Silica Systems Probed by Raman Spectroscopy

2015

We present a Raman study of the effects induced by pressure, thermal treatments, and O2 loading in MCM41, MSU-H, and MSU-F representative mesoporous silica. We compared the starting powders with the mechanically pressed tablets produced applying pressures of ∼0.2 and ∼0.45 GPa. The spectra of the three untreated tablets evidence that the main value of the Si-O-Si angle decreases and that in the MCM41 and the MSU-H Si-O-Si hydrolysis occurs, whereas such a process is absent or much less efficient in the MSU-F. Despite their different networks, the three powders tend to crystallize in cristobalite when treatments are at 1000 °C. The MCM41 and MSU-H tablets exhibit behavior similar to their st…

Materials scienceElectronic Optical and Magnetic MaterialSettore FIS/01 - Fisica SperimentaleMineralogySurfaces Coatings and FilmThermal treatmentMesoporous silicaCristobaliteSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialssymbols.namesakeHydrolysisGeneral EnergyTridymiteEnergy (all)Chemical engineeringPhase (matter)symbolsMoleculePhysical and Theoretical ChemistryRaman spectroscopy
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Charge-transfer interactions between fullerenes and a mesoporous tetrathiafulvalene-based metal–organic framework

2019

The design of metal–organic frameworks (MOFs) incorporating electroactive guest molecules in the pores has become a subject of great interest in order to obtain additional electrical functionalities within the framework while maintaining porosity. Understanding the charge-transfer (CT) process between the framework and the guest molecules is a crucial step towards the design of new electroactive MOFs. Herein, we present the encapsulation of fullerenes (C60) in a mesoporous tetrathiafulvalene (TTF)-based MOF. The CT process between the electron-acceptor C60 guest and the electron-donor TTF ligand is studied in detail by means of different spectroscopic techniques and density functional theor…

Materials scienceFullerenemetal–organic frameworks (MOFs)General Physics and Astronomy010402 general chemistrylcsh:Chemical technology01 natural scienceslcsh:TechnologyFull Research Paperchemistry.chemical_compoundMoleculeNanotechnologyGeneral Materials Sciencelcsh:TP1-1185Electrical and Electronic Engineeringdonor–acceptorPorositylcsh:ScienceMaterials010405 organic chemistrylcsh:TNanotecnologiafullerenecharge transferSorptionlcsh:QC1-9990104 chemical sciencestetrathiafulvalene (TTF)NanoscienceChemical engineeringchemistryDensity functional theoryMetal-organic frameworklcsh:QMesoporous materialTetrathiafulvalenelcsh:PhysicsBeilstein Journal of Nanotechnology
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Modelling of a recirculating photocatalytic microreactor implementing mesoporous N-TiO2 modified with graphene

2020

Abstract The use of microreactors in (photo)catalytic processes offers new possibilities for studying and optimizing many mass and photon transfer limited reactions. In this study, we propose a scalable computational fluid dynamics (CFD) model for the prediction of photocatalytic degradation of a model pollutant (4-nitrophenol) using immobilized N-doped TiO2 grown over reduced graphene oxide (N-TiO2/rGO) in a photocatalytic microreactor working in continuous flow-recirculation mode. The mode of operation used in this study allows the reduction of mass transfer limitations inherent to heterogeneous photocatalytic reactions taking place on immobilized catalysts. A CFD model was developed for …

Materials scienceGeneral Chemical Engineering02 engineering and technology010402 general chemistry01 natural sciencesIndustrial and Manufacturing Engineeringlaw.inventionCatalysisPhotocatalysiAdsorptionlawMass transferMonolayerEnvironmental ChemistryTotal recirculationSettore ING-IND/24 - Principi Di Ingegneria ChimicaGrapheneGeneral ChemistryCFD modelling021001 nanoscience & nanotechnology0104 chemical sciencesMicroreactorChemical engineeringPhotocatalysisSettore CHIM/07 - Fondamenti Chimici Delle TecnologieMicroreactor0210 nano-technologyMesoporous materialChemical Engineering Journal
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Total oxidation of VOCs on mesoporous iron oxide catalysts: Soft chemistry route versus hard template method

2016

9 figures, 3 tables.-- Supplemantary information available

Materials scienceGeneral Chemical EngineeringCatalytic total oxidationOxalic acidInorganic chemistry02 engineering and technology010402 general chemistry01 natural sciencesIndustrial and Manufacturing EngineeringSoft chemistryCatalysisIron oxide catalysts: Soft chemistry synthesischemistry.chemical_compoundPropaneAdsorptionEnvironmental ChemistryNanocastingTotal oxidatioVOCsMesoporous supportSoft chemistry synthesis [Iron oxide catalysts]General Chemistry021001 nanoscience & nanotechnologyToluene oxidation0104 chemical sciencesMesoporous organosilicachemistry0210 nano-technologyMesoporous materialMesoporous α-Fe2O3Template method patternToluene
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Structure and the metal-support interaction of the Au/Mn oxide catalysts

2010

Gold catalysts with loading 1 and 10 wt % were-prepared by deposition precipitation method with urea over mesoporous manganese oxide, obtained through a surfactant-assisted procedure by using cetyltrimethylammonium bromide (CTAB), followed by treatment with sulphuric acid. For comparison, Au(10 wt %) was also deposited over commercial CeO2 and SiO2 supports. The materials were characterized by XRD and EXAFS at the Mn K and Au L-III edges and XPS. Moreover, the analyses were performed on the samples treated under 1%CO/He, at 250 degrees C for 90 min. The structural and surface results of the as prepared manganese oxide confirmed the formation of gamma-MnO2 along with some amorphous Mn3O4 upo…

Materials scienceGeneral Chemical EngineeringInorganic chemistryTEMPERATURE CO OXIDATIONOxideBixbyiteAEROBIC ALCOHOL OXIDATIONCatalysisMetalENHANCED ACTIVITYchemistry.chemical_compoundX-ray photoelectron spectroscopyBromideMANGANESE OXIDERAY-ABSORPTION SPECTROSCOPYBODY DISTRIBUTION-FUNCTIONSMaterials ChemistryCONDENSED MATTERCERIAGeneral ChemistryTEMPERATURE CO OXIDATION; RAY-ABSORPTION SPECTROSCOPY; BODY DISTRIBUTION-FUNCTIONS; AEROBIC ALCOHOL OXIDATION; GOLD NANOPARTICLES; NANOCRYSTALLINE CEO2; ENHANCED ACTIVITY; CONDENSED MATTER; MANGANESE OXIDE; CERIAchemistryvisual_artGOLD NANOPARTICLESNANOCRYSTALLINE CEO2visual_art.visual_art_mediumMesoporous materialHausmannite
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Recent Progress of Microwave-Assisted Synthesis of Silica Materials.

2020

Microwaves are a source of energy of great interest for chemical synthesis. Among nanomaterials, few are as versatile as silica—it forms mesoporous materials and nanoparticles, it can be incorporated as shells or loaded in composites, it can also be functionalized. Despite the relevant properties of silica, and the advantages of the use of microwave as energy source, its use in silica-based materials is not frequent. We report herein a compilation of the research results published in the last 10 years of microwave assisted synthesis of silica based materials. This review includes examples of mesoporous materials for waste removal, catalysis, drug release, and gas adsorption applications, to…

Materials scienceGeneral Chemical EngineeringNanoparticleNanotechnologyReviewengineering.materialNanomaterialsCatalysislcsh:ChemistryAdsorptionlcsh:QD1-999CoatingsilicaengineeringGeneral Materials SciencenanoparticlesMesoporous materialEnergy sourcemicrowave assisted synthesismesoporousMicrowaveNanomaterials (Basel, Switzerland)
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