Search results for " polymers"

showing 10 items of 465 documents

About entangled networks of worm-like micelles: a rejected hypothesis

1996

We report new results from small-angle neutron scattering on d(1 2)-cyclohexane/lecithin/water micellar solutions performed as a function of the water content (w(o)), temperature (T) and dispersed phase volume fraction (phi). The data from dilute samples are interpretable in terms of the existence of giant cylindrical reverse micelles and are well fit with a core-shell model (that provides the micelle structure and dimensions) with values of 28 and 45 Angstrom for the inner core and the outer shell radii, almost independent on temperature and concentration. Such a result could appear consistent with the current idea that worm-like micelles are living polymers. On the contrary, the appearanc…

ORGANOGELSPolymers and PlasticsSANSChemistryInner coreForm factor (quantum field theory)Concentration effectThermodynamicsMineralogyliving polymersNeutron scatteringgelsSmall-angle neutron scatteringMicelleLIGHT-SCATTERINGCondensed Matter::Soft Condensed MatterColloid and Surface ChemistryMICROEMULSIONSMicellar solutionsMaterials Chemistryreverse micellesPhysical and Theoretical ChemistryStructure factorLECITHIN REVERSE MICELLESColloid and Polymer Science
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Slow Dynamics of the Magnetization in One-Dimensional Coordination Polymers: Single-Chain Magnets

2009

18 pages; International audience; Slow relaxation of the magnetization (i.e., "magnet-like" behavior) in materials composed of magnetically isolated chains was observed for the first time in 2001. This type of behavior was predicted in the 1960s by Glauber in a chain of ferromagnetically coupled Ising spins (the so-called Glauber dynamics). In 2002, this new class of nanomagnets was named single-chain magnets (SCMs) by analogy to single-molecule magnets that are isolated molecules displaying related superparamagnetic properties. A long-range order occurs only at T = 0 K in any pure one-dimensional (1D) system, and thus such systems remain in their paramagnetic state at any finite temperatur…

One-dimensional coordination PolymersCondensed matter physics010405 organic chemistryMagnetismChemistryRelaxation (NMR)MagnetismSingle-Chain Magnets010402 general chemistry01 natural sciencesNanomagnet0104 chemical sciencesInorganic ChemistryParamagnetismMagnetizationMagnet[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryGlauberSuperparamagnetism
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Theoretical determination of the geometric and electronic structures of oligorylenes and poli(peri‐naphthalene)

1992

We present a theoretical investigation of the electronic structure of oligorylenes (from perylene to heptarylene, including also the naphthalene molecule) and their corresponding polymer poly(peri‐naphthalene) (PPN) using the nonempirical valence effective (VEH) method. The geometry of the unit cell used to generate the polymer is extrapolated from the PM3‐optimized molecular geometries of the longest oligorylenes. That geometry shows some bond alternation along the perimeter carbon chains and a bond length of ≊1.46 Å is calculated for the peri bonds connecting the naphthalene units. The VEH one‐electron energy level distributions calculated for oligorylenes are used to interpret the experi…

OptimizationChemical BondsBand gapStereochemistryExtrapolationElectric ConductorsGeometryGeneral Physics and AstronomyElectronic structureMolecular physicsEnergy LevelsMolecular orbitalPhysical and Theoretical ChemistryBand Structure:FÍSICA::Química física [UNESCO]Electronic band structurePeryleneFilmsValence (chemistry)Organic PolymersChemistryElectronic Structure ; Perylene ; Naphthalene ; Organic Polymers ; Unit Cell ; Geometry ; Extrapolation ; Optimization ; Chemical Bonds ; Carbon ; Chains ; Energy Levels ; Ionization Potential ; Affinity ; Band Structure ; Electric Conductors ; Films ; PyrolysisUnit CellChainsCarbonUNESCO::FÍSICA::Química físicaBond lengthIonization PotentialMolecular geometryElectronic StructureAffinityIonization energyNaphthalenePyrolysis
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Theoretical study of the effect of substituent and backbone conformation on the electronic properties of symmetrically substituted poly(di‐n‐alkylsil…

1994

We present the results of ab initio 3‐21G∗ geometry optimizations and valence effective Hamiltonian (VEH) band structure calculations aimed at determining the evolution of the geometric and electronic (ionization potential, electron affinities, and band gaps) properties of all‐trans poly(dimethylsilane), poly(diethylsilane), poly(di‐n‐propylsilane), and poly(di‐n‐butylsilane) when increasing the size of the alkyl group. In the latter polymer, we have also studied the 7/3 conformation, in order to analyze the effect of the backbone conformation on the geometric and electronic structure. The VEH ionization potentials of all‐trans poly(di‐n‐alkylsilanes) are almost equal, and as experimental p…

OptimizationEnergy GapPropyl CompoundsBand gapAb initioSubstituentGeometryGeneral Physics and AstronomyElectronic structurechemistry.chemical_compoundAb initio quantum chemistry methodsComputational chemistryMethyl CompoundsConformational ChangesPhysical and Theoretical ChemistryBand Structure:FÍSICA::Química física [UNESCO]Electronic band structureAlkyl Compounds ; Silanes ; Organic Polymers ; Conformational Changes ; Ab Initio Calculations ; Geometry ; Optimization ; Band Structure ; Affinity ; Ionization Potential ; Energy Gap ; Methyl Compounds ; Ethyl Compounds ; Propyl CompoundsDimethylsilaneOrganic PolymersSilanesUNESCO::FÍSICA::Química físicaCrystallographyAlkyl CompoundsIonization PotentialAffinitychemistryEthyl CompoundsIonization energyAb Initio Calculations
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Nanoscale control in organic bulk heterojunctions of new set of materials for photovoltaic applications

2008

Organic PhotovoltaicScanning Force Microscopy (SFM)Solar EnergyConductive Polymers
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Boramers for Photovoltaic Applications

2008

Organic PhotovoltaicScanning Force Microscopy (SFM)Solar EnergyConductive Polymers
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Generation of white LED light by frequency downconversion using a perylene-based dye

2012

A high efficiency white light emitting diode (LED) was fabricated by generation of frequency down-conversion from a GaN/InGaN blue LED. In place of conventional inorganic phosphors, a perylene-based dye was used for colour conversion. The resulting hybrid structure is analysed by focusing on the visual performance of the realised LEDs employing the most relevant photometric parameters of a light source. Preparation of the organic polymer is described as well. The thermal stability of the dye was investigated and a simple structure which avoids colour degradation is proposed.

Organic polymerMaterials sciencebusiness.industryPhosphordyes light emitting diodes phosphors polymers wide band gap semiconductors GaN-InGaN blue LED colour conversionSettore ING-INF/01 - Elettronicalaw.inventionchemistry.chemical_compoundOpticsLight sourcechemistrylawOptoelectronicsDegradation (geology)Thermal stabilityElectrical and Electronic EngineeringbusinessPeryleneDiodeLight-emitting diode
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Bulk heterojunctions by boramers for plastic photovoltaics

2009

Organic semiconductors conductive polymers plastic solar cells thin films bulk heterojunctions
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Preparation of pH sensitive poly(vinilydenefluoride) porous membranes by grafting of acrylic acid assisted by supercritical carbon dioxide

2012

Free radical grafting of acrylic acid (AA) on poly(vinilydenefluoride) (PVDF) porous membranes was studied at 65°C using supercritical carbon dioxide (scCO 2) as a solvent and delivery agent. The process was initiated by the thermal decomposition of benzoylperoxide (BPO). Spectroscopic analyses confirmed the presence of poly(AA) chains linked to treated membranes. The mass fraction of grafted AA increased with grafting time and BPO concentration while it decreased when the density of the fluid phase was enhanced. A not-monotonic trend was obtained when the effect of the initial AA concentration was studied. The grafting process was accompanied by a reduction of the crystallinity of the PVDF…

PH-dependentGrafting proceGeneral Chemical EngineeringRadical polymerizationpH-sensitive polymersMass fractionPoly(vinylidene fluoride)Free radical graftingGrafting degreeCarboxylic acidRelease experimentAcrylic acidSupercritical fluid extraction Grafting (chemical)chemistry.chemical_compoundCrystallinityPVDF membraneFree radicalPolymer chemistrypH sensorPhysical and Theoretical ChemistryFluid-phasepH sensitiveAcrylic acidCrystallinitieDecompositionSupercritical carbon dioxideFree radical polymerizationChemistrySupercritical carbon dioxides Carbon dioxideSettore ING-IND/27 - Chimica Industriale E TecnologicaCondensed Matter PhysicsGraftingSolventMembraneSpectroscopic analysiPorous membraneNuclear chemistryThe Journal of Supercritical Fluids
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Resource or waste? A perspective of plastics degradation in soil with a focus on end-of-life options.

2018

‘Capable-of-being-shaped’ synthetic compounds are prevailing today over horn, bone, leather, wood, stone, metal, glass, or ceramic in products that were previously left to natural materials. Plastic is, in fact, economical, simple, adaptable, and waterproof. Also, it is durable and resilient to natural degradation (although microbial species capable of degrading plastics do exist). In becoming a waste, plastic accumulation adversely affects ecosystems. The majority of plastic debris pollutes waters, accumulating in oceans. And, the behaviour and the quantity of plastic, which has become waste, are rather well documented in the water, in fact. This review collects existing information on pla…

PLA polylactic acidPS polystyreneETS European Emissions Trading schemePOM polyoxymethyleneHMC heat melt compactor technology02 engineering and technology010501 environmental sciencesNHV net habitable volumeLDPE low-density polyethylene01 natural sciencesPC polycarbonateResin identification codeLCP liquid crystal polymerslcsh:Social sciences (General)PAC pro-oxidant additive containingPET polyethylene terephthalateEPR Extended Producers ResponsibilityMultidisciplinaryWaste managementNatural materials021001 nanoscience & nanotechnologyPU or PUR polyurethaneSettore AGR/02 - Agronomia E Coltivazioni ErbaceeEPS expandable polystyreneRIC resin identification codeSettore AGR/14 - PedologiaPVDF polydifluoroethylenelcsh:H1-990210 nano-technologyBiogeoscienceGPPS Polystyrene (General Purpose)PVC polyvinyl chlorideResource (biology)Polymethyl methacrylatePA polyamidePBT polybutylene terephthalatePSU polyarylsulfonePTFE polytetrafluoroethylenePMMA polymethyl methacrylatePHA polyhydroxyalkanoateMicrobiologyPEEK polyaryletheretherketoneArticleEnvironmental scienceEnvironmental science Biogeoscience Industry MicrobiologyPPA polyphthalamideTPE thermoplastic polyester elastomerNatural degradationIndustryPPS polyphenylene sulphidelcsh:Science (General)ABS acrylonitrile-butadiene-styrene0105 earth and related environmental sciencesbusiness.industryPP polypropyleneHDPE high-density polyethyleneBPA bisphenol AHBCD hexabromocyclododecaneFuture studyAgricultureDOM dissolved organic matterDegradation (geology)Environmental sciencebusinesslcsh:Q1-390Heliyon
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