Search results for "Organo"

showing 10 items of 1460 documents

Efficient Gas Separation and Transport Mechanism in Rare Hemilabile Metal–Organic Framework

2019

Understanding/visualizing the established interactions between gases and adsorbents is mandatory to implement better performance materials in adsorption/separation processes. Here we report the unique behavior of a rare example of a hemilabile chiral three-dimensional metal–organic framework (MOF) with an unprecedented qtz-e-type topology, with formula CuII2(S,S)-hismox·5H2O (1) (hismox = bis[(S)-histidine]oxalyl diamide). 1 exhibits a continuous and reversible breathing behavior, based on the hemilability of carboxylate groups from l-histidine. In situ powder (PXRD) and single crystal X-ray diffraction (SCXRD) using synchrotron radiation allowed us to unveil the crystal structures of four …

Materials scienceGeneral Chemical EngineeringQuímica organometàl·lica02 engineering and technologyCrystal structure010402 general chemistry01 natural scienceschemistry.chemical_compoundAdsorptiontransport mechanismMaterials ChemistryGas separationCarboxylateQuímica InorgánicaGas separationGeneral ChemistryMetal Organic FrameworkCiència dels materials021001 nanoscience & nanotechnologyEfficient gas separation0104 chemical scienceschemistryHemilabilityPhysical chemistryRare hemilabile metal-organic frameworkmixed matrix membranesMetal-organic frameworkTransport mechanism0210 nano-technologySingle crystalPowder diffractionChemistry of Materials
researchProduct

Integrated Cleanroom Process for the Vapor-Phase Deposition of Large-Area Zeolitic Imidazolate Framework Thin Films

2019

Chemistry of materials XX(XX), acs.chemmater.9b03435 (2019). doi:10.1021/acs.chemmater.9b03435

Materials scienceGeneral Chemical EngineeringQuímica organometàl·licaNanotechnology02 engineering and technologyGeneral ChemistryChemical vapor depositionCiència dels materials540010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesCleanroomScientific methodddc:540Materials ChemistryDeposition (phase transition)Metal-organic frameworkElectronicsThin filmÒxids0210 nano-technologyZeolitic imidazolate frameworkChemistry of Materials
researchProduct

Evaluation of aging processes of petroleum asphalt cements by solid state electrochemical monitoring

2018

Abstract The changes in the chemistry of organosulfur compounds from asphalt cements during aging are studied using solid state voltammetry of immobilized microparticles. Five Brazilian asphalt cements were evaluated after three forced aging processes: Rolling Thin Film Oven Test (RTFOT), Pressure Aging Vessel (PAV) and SUNTEST. It was possible to identify the presence of thiophenes, sulfides and sulfoxides in the different samples and the reactional changes during the aging processes were proposed. Voltammetric data, supported by ATR-FTIR spectroscopy, indicate that aging asphalts involve the increase of the proportion of sulfoxide and thiophene components and that polythiophene compounds …

Materials scienceGeneral Chemical EngineeringSulfoxide02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyElectrochemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryChemical engineeringAsphaltElectrochemistryThiophenePolythiopheneThin film0210 nano-technologyVoltammetryOrganosulfur compoundsElectrochimica Acta
researchProduct

Recombination in Perovskite Solar Cells

2017

Trap-assisted recombination, despite being lower as compared with traditional inorganic solar cells, is still the dominant recombination mechanism in perovskite solar cells (PSCs) and limits their efficiency. We investigate the attributes of the primary trap assisted recombination channels (grain boundaries and interfaces) and their correlation to defect ions in PSCs. We achieve this by using a validated device model to fit the simulations to the experimental data of efficient vacuum-deposited p-i-n and n-i-p CH3NH3PbI3 solar cells, including the light intensity dependence of the open circuit voltage and fill factor. We find that, despite the presence of traps at interfaces and grain bounda…

Materials scienceLetterEFFICIENCYMETHYLAMMONIUM LEAD IODIDEMIGRATIONEnergy Engineering and Power TechnologyNanotechnology02 engineering and technologyQuantum dot solar cell010402 general chemistryFILMS01 natural sciencesIonMaterials ChemistryORGANOMETAL TRIHALIDE PEROVSKITEVOLTAGEHYSTERESISPerovskite (structure)Theory of solar cellsRenewable Energy Sustainability and the EnvironmentHybrid solar cellELECTRICAL-PROPERTIES021001 nanoscience & nanotechnologySURFACE-DEFECTSTRANSPORT0104 chemical sciencesLight intensityFuel TechnologyChemistry (miscellaneous)Chemical physicsGrain boundary0210 nano-technologyRecombinationACS Energy Letters
researchProduct

H3PW12O40 supported on mesoporous MCM-41 and Al-MCM-41 materials: preparation and characterisation

2011

MCM-41 and Al–MCM-41 has been synthesized using cetyl-trimethylammonium bromide (CTAB) surfactant as template and adding the silica precursor to aqueous solutions containing CTAB. The obtained solids were calcined at 600 °C for 4 h. HPW heteropolyacid supported on the mesoporous were prepared using the incipient wetness method. The characterization of materials was performed by X-ray diffraction, Transmission Electron Microscopy, N2 adsorption, 29Si Cross Polarization–Magic Angle Spinning and 27Al MAS NMR. Results showed that the hexagonal structure is obtained in both cases. The Aluminium species are located inside an extra-framework. The impregnation reduces the surface area of the mesopo…

Materials scienceMechanical EngineeringInorganic chemistrychemistry.chemical_elementlaw.inventionSilanolchemistry.chemical_compoundMesoporous organosilicaAdsorptionSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryMCM-41Chemical engineeringMechanics of MaterialsAluminiumlawMagic angle spinningGeneral Materials ScienceCalcinationMesoporous materialMCM-41 aluminum 27Al MAS NMR.Settore CHIM/02 - Chimica Fisica
researchProduct

Nano-sized mesoporous carbon particles with bimodal pore system and semi-crystalline porous walls

2008

Acetylene CVD carbon replication of a hierarchical pore silica-based material, Fe-UVM-7, is reported. The original template organization, which is based on the aggregation of mesoporous nanoparticles, is accurately replicated in the final carbon material: a bimodal porous carbon combining mesoporous nanoparticles and inter-particle textural-like pores which provide high surface area, a highly accessible pore system and semi-crystalline pore walls in the form of graphitic-like nanodomains is presented.

Materials scienceMechanical EngineeringNanoparticlechemistry.chemical_elementChemical vapor depositionCondensed Matter PhysicsNanomaterialsMesoporous organosilicachemistryMechanics of MaterialsCarbide-derived carbonGeneral Materials ScienceComposite materialMesoporous materialPorosityCarbonMaterials Letters
researchProduct

Synthesis of a Hydrothermally Stable, Periodic Mesoporous Material Containing Magnetite Nanoparticles, and the Preparation of Oriented Films

2006

Magnetite nanoparticles modified covalently with triethoxysilane having a quaternary dicetyl ammonium ion are used together with tetraethylorthosilicate as building blocks to prepare a mesoporous material. Cetyltrimethylammonium bromide is used as a structure-directing agent under conditions typically used for mesoporous MCM-41 silicas. The resulting mesoporous material (MAG-MCM-41), containing up to 15 wt % of magnetite is characterized by transmission electron microscopy (TEM), isothermal gas adsorption, and X-ray diffraction. In contrast to siliceous MCM-41, mesoporous MAG-MCM-41 exhibits a remarkable hydrothermal stability. The magnetic properties of MAG-MCM-41 are characterized by DC a…

Materials scienceMineralogyCondensed Matter PhysicsMagnetic susceptibilityHydrothermal circulationElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundMesoporous organosilicaAdsorptionchemistryChemical engineeringTransmission electron microscopyTriethoxysilaneElectrochemistryMesoporous materialMagnetiteAdvanced Functional Materials
researchProduct

Enhanced surface area in thermally stable pure mesoporous TiO2

2000

Abstract We describe here for the first time the surfactant-assisted synthesis of thermally stable mesoporous pure TiO 2 having a high surface area. Our synthetic approach to the chemistry of this system is based on the equilibrium between the hydrolysis and condensation reactions of the inorganic species and the organic–inorganic self-assembling processes. The use of titanatrane complexes helps to retard the hydrolysis and condensation reactions, thus allowing us to overcome the difficulties in preparing titanium dioxide mesoporous materials starting from highly reactive Ti-alkoxides. The mesoporous material has been characterized by TEM, XRD and N 2 adsorption–desorption isotherms and dis…

Materials scienceMineralogyGeneral ChemistryCondensed Matter PhysicsCondensation reactionMesoporous organosilicaHydrolysischemistry.chemical_compoundChemical engineeringchemistryTransmission electron microscopyX-ray crystallographyTitanium dioxideGeneral Materials ScienceThermal stabilityMesoporous materialSolid State Sciences
researchProduct

Incorporation of Mn12single molecule magnets into mesoporous silica

2003

The incorporation of four Mn12 derivatives, namely [Mn12O12(O2CR)16(H2O)4] (R = CH3 (1), CH3CH2 (2), C6H5 (3), C6F5 (4)), into the hexagonal channels of the MCM-41 mesoporous silica has been studied. Only the smallest clusters 1 and 2, i.e. those with compatible size with the pores of MCM-41, could enter into the mesoporous silica. Powder X-ray diffraction analysis, HRTEM images and N2 adsorption–desorption isotherm experiments show that the well-ordered hexagonal structure of MCM-41 is preserved and that the Mn12 clusters are inside the pores. The magnetic properties of the MCM-41/2b nanocomposite material obtained in CH2Cl2 indicate that the structure of the cluster is maintained after in…

Materials scienceNanocompositeMineralogyNanoparticleGeneral ChemistryMesoporous silicalaw.inventionMesoporous organosilicachemistry.chemical_compoundchemistryChemical engineeringlawMaterials ChemistryCalcinationCarboxylateMesoporous materialHigh-resolution transmission electron microscopyJ. Mater. Chem.
researchProduct

Compatibilized Polyamide 6/Polyethylene Blends Clay Nanocomposites: Effect of the Degradation and Stabilization of the Clay Modifier

2008

Abstract Blends of polyamide 6 (PA6) and high-density polyethylene (HDPE) were compatibilized using an already investigated method and a sample of Cloisite 15A, a montmorillonite modified with ammonium quaternary salts was added. The blends were prepared in a twin screw extruder and characterized from a morphological, rheological and mechanical point of view. The results indicated that, despite a good morphology achieved in the filled blends and a moderate intercalation of the clay, the mechanical properties are far from being good, especially the ultimate properties. In order to investigate the possible influence of the inhibition of the crystallization and of the degradation of the organi…

Materials scienceNanocompositeNanocompositePolymers and PlasticsCompatibilizationPolyethyleneCondensed Matter PhysicsStabilizationlaw.inventionchemistry.chemical_compoundDegradationMontmorilloniteSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryMechanics of MaterialslawMaterials ChemistryOrganoclayPolymer blendHigh-density polyethyleneCrystallizationComposite materialOrganoclayCompatibilization
researchProduct