Search results for "Lene"

showing 10 items of 4480 documents

Anisotropic Stick-slip friction of highly oriented thin films of poly(tetrafluoroethylene) at the molecular level

1996

Lateral force microscopy (LFM) studies of poly(tetrafluoroethylene) (PTFE) films with molecular resolution are reported. Thin PTFE layers with a high degree of orientation were obtained by pressing and sliding a block of polymer on a clean, heated muscovite mica substrate. LFM nanographs obtained on these films by scanning at directions between ca. 40 and 90° with respect to the film orientation direction, i.e. with respect to the direction of the polymer chains, showed a “stick-slip” type frictional motion of the LFM probe tip at the molecular level. The friction force observed at constant load decreased with decreasing scan angles. Chain-chain packing distances obtained by LFM and contact…

chemistry.chemical_classificationPressingMaterials scienceMechanical EngineeringMuscoviteNanotechnologySurfaces and InterfacesPolymerSlip (materials science)engineering.materialSurfaces Coatings and Filmschemistry.chemical_compoundchemistryMechanics of MaterialsMicroscopyengineeringTetrafluoroethyleneComposite materialThin filmAnisotropyTribology letters
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Influence of preparation conditions of nano-crystalline ceria catalysts on the total oxidation of naphthalene, a model polycyclic aromatic hydrocarbon

2007

Abstract Nano-crystalline ceria catalysts prepared by homogeneous precipitation with urea were tested for the total oxidation of naphthalene, a model polycyclic aromatic hydrocarbon (PAH). Systematic variation of preparation conditions, including calcination temperature, calcination time and aging time, resulted in differences in surface area, reducibility, morphology and crystallite size of the CeO 2 catalyst and hence differences in catalytic performance. A combination of high surface area, small crystallite size and high oxygen defect concentration was found to favor the efficiency of the ceria catalysts for the total oxidation of naphthalene. Optimum preparation conditions for this stud…

chemistry.chemical_classificationProcess Chemistry and TechnologyInorganic chemistryPolycyclic aromatic hydrocarbonHeterogeneous catalysisCatalysisCatalysislaw.inventionchemistry.chemical_compoundHydrocarbonCatalytic oxidationchemistrylawCalcinationCrystalliteGeneral Environmental ScienceNaphthaleneApplied Catalysis B: Environmental
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1-Alkyl- and azeto[1,2-a][1,5]benzodiazepine derivatives in the reaction of o-phenylenediamine with 3-(dimethylamino)propiophenones

2000

The reaction of o-phenylenediamine (4) with one, two or three equivalents of p-substituted 3-dimethylaminopropiophenone hydrochlorides 5a−e was studied. 4-Aryl-2,3-dihydro-1H-1,5-benzodiazepine derivatives 6a−e were obtained in good yields, along with the 1:2-adducts 7c−e and the unexpected 1:3-adducts rac-8c−e. The type of adduct formed is determined by the molar ratio of the reactants 4 and 5 and by the nature of the substituent in the para position of the propiophenone 5.

chemistry.chemical_classificationPropiophenonesBenzodiazepineChemistrymedicine.drug_classOrganic ChemistrySubstituentMedicinal chemistryAdductPara positionchemistry.chemical_compoundPropiophenoneo-PhenylenediaminemedicinePhysical and Theoretical ChemistryAlkyl
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Rheological behaviour, filmability and mechanical properties of biodegradable polymer films

2014

The rheological properties in shear flow and non isothermal elongational flow of two biodegradable polymers, belonging to two different classes of materials, have been measured and compared with those of a film blowing grade high density polyethylene in order to assess the filmability of these polymers. The mechanical properties of isotropic and anisotropic samples have been also reported.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceIsotropytechnology industry and agriculturePolymerBiodegradable polymerIsothermal processCondensed Matter::Soft Condensed MatterRheologychemistryHigh-density polyethyleneComposite materialAnisotropyShear flowbiodegradable filmAIP Conference Proceedings
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Electronic structure of polysilanes: influence of substitution and conformation

1993

Abstract The valence effective Hamiltonian (VEH) quantum-chemical approach is used to investigate the electronic properties of polysilane. The valence band structure calculated for this fully saturated polymer is analyzed in terms of orbital contributions and compared to that of the closely related carbon polymer, polyethylene. The effects of alkyl substitution and silicon backbone conformation are studied by elucidating the modifications that these structural changes induce on the electronic valence band structure of all-trans unsubstituted polysilane. The VEH results predict a decrease of the band gap upon alkyl substitution and on going from helical to all-trans conformations.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesValence (chemistry)SiliconBand gapMechanical EngineeringMetals and Alloyschemistry.chemical_elementPolymerElectronic structurePolyethyleneCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundsymbols.namesakeCrystallographychemistryMechanics of MaterialsComputational chemistryMaterials ChemistrysymbolsPolysilaneHamiltonian (quantum mechanics)Synthetic Metals
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Antimicrobial activity of methylene blue and toluidine blue O covalently bound to a modified silicone polymer surface

2009

Methylene Blue or Toluidine Blue O were covalently bound to an activated silicone polymer by means of an amide condensation reaction. UV-visible absorption spectra confirmed that the dye was surface bound. The new polymers with covalently attached dye display significant bactericidal activity against Escherichia coli and Staphylococcus epidermidis with a 99.999% reduction in viable bacteria after four minutes exposure to a low power laser.

chemistry.chemical_classificationRMAbsorption spectroscopybiologyGeneral ChemistryPolymerPhotochemistrybiology.organism_classificationCondensation reactionmedicine.disease_causeRSchemistry.chemical_compoundchemistryCovalent bondStaphylococcus epidermidisAmidePolymer chemistryMaterials ChemistrymedicineEscherichia coliMethylene blueJournal of Materials Chemistry
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Physical and structural characterization of blends made with polyamide 6 and gamma-irradiated polyethylenes

1996

Abstract Morphological, calorimetric and rheological results of blends made with polyamide 6 and polyethylene gamma irradiated in air are presented. The polar oxidized groups grafted in the poliolefin chains through gamma-radiation induce “compatibilization” effects in the blends with a more uniform and finer distribution of the polyethylene “phase” in the polyamide matrix, with respect to blends made with the unirradiated polymer. This effect, observed with polyethylenes of different molecular structure, i.e. low density, linear low density and high density, was attributed to the presence of interactions among the functional oxidized groups of the polyethylene chains and the polyamide. Tes…

chemistry.chemical_classificationRadiationMaterials sciencePolymerCompatibilizationPolyethylenechemistry.chemical_compoundchemistryRheologyChemical engineeringPhase (matter)PolyamidePolymer chemistryMoleculeIrradiationRadiation Physics and Chemistry
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Carboxylation of a linear low density polyethylene via gamma irradiation in presence of carbon dioxide in subcritical and supercritical conditions

1994

Abstract In this work the molecular modifications induced in a linear low density polyethylene gamma irradiated in presence of carbon dioxide both in subcritical and supercritical conditions are presented. The obtained results indicate that this process can be a new and interesting way in order to graft oxidized groups in the polyethylene chains. Moreover it is worth noting that, together with these functionalization reactions, also a significant crosslinking occurs, with improvement in some mechanical tensile behaviour.

chemistry.chemical_classificationRadiationMaterials sciencePolymerPolyethyleneSupercritical fluidLinear low-density polyethylenechemistry.chemical_compoundchemistryPolymerizationCarboxylationChemical engineeringCarbon dioxideCompounds of carbonNuclear chemistryRadiation Physics and Chemistry
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Molecular modifications—Mechanical behaviour relationships for gamma irradiated LLDPE/PA6 blends

1994

Abstract The molecular modifications, due to γ radiation under vacuum, of linear low density polyethylene/polyamide 6 blends are presented and related to their mechanical behaviour. Solubility and melt viscosity tests indicate that in blends the polyethylene component undergoes mainly crosslinking phenomena, whereas the main effect on polyamide is chain branching. According to these molecular modifications, the most relevant effect is the increase of the tensile modulus for the polyethylene rich blends and the increase of the impact strength for the polyamide rich blends.

chemistry.chemical_classificationRadiationMaterials scienceeducationtechnology industry and agricultureYoung's modulusIzod impact strength testPolymerPolyethyleneBranching (polymer chemistry)Linear low-density polyethylenesymbols.namesakechemistry.chemical_compoundPolymerizationchemistryPolymer chemistryPolyamidesymbolsComposite materialRadiation Physics and Chemistry
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Charge Transfer Salts Based on Polyoxometalates and Seleno-Substituted Organic Donors. Synthesis, Structure, and Magnetic Properties of (BEST)3H[PMo1…

1998

Electrochemical oxidation of the tetrathiafulvalene (TTF) type organic donor bis(ethylenediseleno)tetrathiafulvalene (BEST) in the presence of the Keggin polyoxometalate [PMo12O40]3- affords the radical salt formulated as (BEST)3H[PMo12O40] (crystal data:  triclinic, space group P1 with a = 13.056(1) A, b = 13.957(1) A, c = 22.302(3) A, α = 97.019(9)°, β = 94.17(1)°, γ = 95.847(9)°, and Z = 2). This is the first salt of a selenium-containing donor with a polyoxometalate cluster. The structure of this organic/inorganic hybrid consists of layers of the organic donors that alternate with polyoxometalate layers in the c direction. The organic molecules, which are completely ionized, form two ty…

chemistry.chemical_classificationRadicalInorganic chemistrySalt (chemistry)Triclinic crystal systemElectrochemistryMagnetic susceptibilityInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryPolyoxometalateCluster (physics)Physical and Theoretical ChemistryTetrathiafulvaleneInorganic Chemistry
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