Search results for "init"

showing 10 items of 6629 documents

Modeling the non-linear deformation of a short-flax-fiber-reinforced polymer composite by orientation averaging

2013

Abstract The growing usage of short-flax-fiber-reinforced polymer composites in such applications as automotive industry necessitates the prediction of their mechanical response up to and beyond the limit of elasticity. Due to the imperfect, mechanical interlocking-dominated adhesion of natural fibers to most polymers, both fiber debonding and matrix yielding contribute to the non-linear deformation. In the present study, the deformation under an active loading of a short misaligned fiber composite is modeled by the orientation averaging approach, employing an analytical description of the behavior of a unit cell (UC), the parameters of which are determined using a FEM analysis of UC respon…

chemistry.chemical_classificationMaterials scienceTension (physics)Mechanical EngineeringComposite numberPolymerElasticity (physics)Deformation (meteorology)Industrial and Manufacturing EngineeringFinite element methodNonlinear systemchemistryMechanics of MaterialsCeramics and CompositesFiberComposite materialComposites Part B: Engineering
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Theoretical study of asymmetrically substituted poly(organosilanes)

1994

Summary form only given. Poly(organosilanes) [-SiRR'-] where R and R' represent various alkyl and aryl groups, are the subject of intense scientific and technological interest because of the interesting properties such as, intense near-UV absorption, highly efficient photoluminiscence, non-linear optical properties, these polymers present. In this contribution, we present the electronic structure of some asymmetrically substituted poly(organositanes). We have focused the study on the effect of the tacticity on the electronic structure of the polymer. We have employed ab initio methods to obtain reliable geometrical parameters. The band structure calculations have been performed using the va…

chemistry.chemical_classificationMaterials scienceValence (chemistry)ArylAb initioPolymerElectronic structurechemistry.chemical_compoundchemistryTacticityPhysical chemistryOrganic chemistryElectronic band structureAlkylInternational Conference on Science and Technology of Synthetic Metals
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3,3'-Bicarbazole structural derivatives as charge transporting materials for use in OLED devices

2018

In this study we report novel 3,3′-bicarbazole based charge transporting materials mainly designed for a use in systems containing phosphorescent iridium (III) complex emitters. A low-cost oxidative coupling reaction using FeCl3 was employed in the synthesis of 3,3′-bicarbazole compounds. Different derivatives of 3,3′-bicarbazole with 4-ethoxyphenyland ethyl- substituents at 9,9′- positions and (2,2-diphenylhydrazono)methyl- and 4-(dimethylamino)styryl- substituents at 6,6′- positions were synthesized. Obtained (2,2-diphenylhydrazono)methyl- derivatives exhibit glass transition temperatures that are sufficient for applications in electronic devices. Thin amorphous films of good optical qual…

chemistry.chemical_classificationMaterials sciencechemistryElectron affinityOLEDPhysical chemistrychemistry.chemical_elementMoleculeIridiumElectron acceptorGlass transitionPhosphorescenceAmorphous solidOrganic Electronics and Photonics: Fundamentals and Devices
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Crystallization kinetics of LDPE/Ny6 blends

1988

The crystallization behaviour of low density polyethylene/nylon 6 blends has been investigated as a function of the composition. The melting points of the polymers are almost uninfluenced by the presence of the other homopolymers except for blends with a nylon content of 75–90%. Blends with 10% nylon content do not exhibit the crystallization peak during the cooling step probably because of the low concentration and high viscosity of the low density polyethylene matrix. The crystallinity degree of the polyethylene is independent of the composition, while some variations are shown by the polyamide. Finally the rate of nucleation is strongly affected by the composition, in particular for the …

chemistry.chemical_classificationMaterials sciencetechnology industry and agricultureNucleationPolymerPolyethylenelaw.inventionLow-density polyethylenechemistry.chemical_compoundCrystallinityNylon 6chemistryChemical engineeringlawPolymer chemistryMelting pointCrystallizationJournal of thermal analysis
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Design and Optimization of Chromophores for Liquid Crystal and Photorefractive Applications

1999

ABSTRACTOrganic chromophores have been exploited for a wide range of discrete optical and electronic functions as well as a growing number of combined opto-electronic functions. We are pursuing development of organic and polymer materials for a range of applications that require properties including liquid crystallinity, second order optical nonlinearity, photorefractivity and, more recently, special nonlinear optical behavior involving molecular chirality.

chemistry.chemical_classificationMolecular dynamicsCrystallinityMaterials sciencechemistryLiquid crystalPhysics::OpticsNonlinear opticsNanotechnologyPhotorefractive effectPolymerChromophoreChirality (chemistry)MRS Proceedings
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Photoaffinity cross-linking of F1ATPase from the thermophilic bacterium PS3 by 3′-arylazido-β-alanyl-2-azido ATP

1989

AbstractThe photoactivatable bifunctional 3′-arylazido-β-alanyl-2-azido ATP (2,3′-DiN3ATP) has been applied to study the localization of the nucleotide-binding sites of coupling factor 1 (F1ATPase, TF1) from the thermophilic bacterium PS3 by photoaffinity cross-linking. UV irradiation of TF1 in the presence of 2,3′-DiN3ATP results in the nucleotide-dependent formation of various higher molecular mass cross-links formed by two, three or even four α- and/or β-subunits. The differences observed upon photoaffinity cross-linking by the bifunctional 2-azido ATP or 8-azido ATP analog are discussed. They are probably due to the varied maximal distance between both azido groups, or to the different …

chemistry.chemical_classificationMolecular massbiologyStereochemistryProtein subunitNucleotide conformationBiophysicsCell Biologybiology.organism_classificationBiochemistrychemistry.chemical_compoundEnzymechemistryStructural BiologyGeneticsPhotoaffinity crosslinkingATPase F1-NucleotideNucleotide-binding siteBinding siteBifunctionalInterfacial localizationMolecular BiologyThermophilic bacterium PS3BacteriaFEBS Letters
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Organoclay Nanocomposites from Ethylene-Acrylic Acid Copolymers

2006

A study of the structure–property relationships for nanocomposites prepared by melt compounding from ethylene–acrylic acid copolymers of varied composition and molecular architecture, and organoclays modified with different ammonium ions has been made by DSC, POM, SEM, TEM, WAXD, and rheological and mechanical tests. Within the series of clays investigated, the best levels of dispersion were displayed by those organically modified with quaternary ammonium ions containing two long alkyl tails. The relevant nanocomposites were shown to possess mixed exfoliated and intercalated morphology. The spacing of the intercalated clay stacks, most of which comprise few silicate layers, was found to be …

chemistry.chemical_classificationNanocompositeMaterials sciencePolymers and PlasticsGeneral Chemical EngineeringOrganic ChemistryPolymerchemistry.chemical_compoundCrystallinityMontmorillonitechemistryMaterials ChemistryCopolymerOrganoclayComposite materialIonomerAlkyl
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Controlled solvent vapour annealing for polymer electronics

2009

Solvent vapour annealing (SVA) is demonstrated as an attractive method to anneal polymer blend and block copolymer thin films at low temperatures. It is especially suitable for organic electronics, where sensitive materials with strong intermolecular interactions are used. We demonstrate the effect of solvent vapour exposure on the film properties of a perylene bisimide acrylate (PPerAcr) side-chain polymer with strong crystallinity at the perylene bisimide moieties. We record the film thickness, light absorption and fluorescence as a function of the relative solvent vapour pressure. At a certain threshold of relative solvent vapour pressure, we observe a disruption of the π–π stacking, whi…

chemistry.chemical_classificationOrganic electronicsMaterials scienceAnnealing (metallurgy)General ChemistryPolymerCondensed Matter PhysicsSolventchemistry.chemical_compoundCrystallinitychemistryChemical engineeringPolymer chemistryPolymer blendThin filmPeryleneSoft Matter
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Analysis of plasticization and reprocessing effects on the segmental cooperativity of polylactide by dielectric thermal spectroscopy

2021

Abstract In the present study, the dielectric properties of both neat and plasticized polylactide submitted to repeated extrusion and injection processes to simulate recycling were analysed. The dielectric relaxation spectrum, consisting of β and α relaxation, revealed the relevance of both acryl-PEG based plasticization and thermo-mechanical degradation induced by repeated extrusion and grinding-injection reprocessing cycles on polylactide (PLA). The β-relaxation has its origin in the intramolecular local motions of pendant groups of the PLA backbone, while the α-relaxation is representative of the intermolecular large-scale segmental motions of the PLA backbone. The addition of acryl-PEG …

chemistry.chemical_classificationPermittivityMaterials sciencePolymers and PlasticsOrganic ChemistryIntermolecular forceRelaxation (NMR)02 engineering and technologyDielectricPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesCrystallinityChemical engineeringchemistryMaterials ChemistryExtrusion0210 nano-technologyGlass transitionPolymer
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Photoaffinity labeling of the coupling factor 1 from the thermophilic bacterum PS3 by 8-azido ATP

1984

AbstractTo localize the nucleotide binding sites of the F1ATPase (TF1) from the thermophilic bacterium PS3 we have used 14C-labeled 8-azido ATP (8-N3ATP) as photoaffmity label. 8-N3ATP is hydrolyzed by the F,ATPase in the absence of ultraviolet light. Irradiation by ultraviolet light of the enzyme in the presence of 8-N3ATP results in reduction of ATPase activity and in preferential nucleotide specific labeling of the α subunits (0.8–0.9 mol 8-N3ATP/TF1,α:β = 4:1). Inactivation and labeling do not depend on the presence of Mg2+. Both effects decrease upon addition of various nucleotide di- or triphosphates.

chemistry.chemical_classificationPhotoaffinity labelingStereochemistryNoncatalytic nucleotide binding siteThermophileBiophysicsCell BiologyBiochemistryCoupling (electronics)HydrolysisEnzymechemistryStructural BiologyPhotoaffinity labelingMoleBacterial F1ATPaseGeneticsUltraviolet lightCatalytic nucleotide binding siteNucleotideThermophilic bacterium PS3Molecular BiologyFEBS Letters
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