Search results for "Activation"

showing 10 items of 2079 documents

Phonon coupling of non-bridging oxygen hole center with the silica environment: Temperature dependence of the 1.9 eV emission spectra

2008

Abstract We report an experimental study on the shape of the 1.9 eV emission associated with non-bridging oxygen hole centers in silica and its temperature dependence, from 4 up to 300 K, under visible and ultraviolet excitation. Our analysis points out that these defects are coupled with their environment by phonons whose contribution can be described by the single mode of mean frequency between 300–400 cm −1 and Huang–Rhys factor of ∼3. On increasing the temperature, the luminescence intensity undergoes a thermal quenching caused by non-radiative processes, its deviation from a pure Arrhenius law can be accounted for by an uniform distribution of activation energy, from 0.002 to 0.05 eV. …

Arrhenius equationPhotoluminescenceLuminescenceChemistryPhononBiophysicsSilicaGeneral ChemistryActivation energyCondensed Matter PhysicsPhonon couplingBiochemistryAtomic and Molecular Physics and OpticsPoint defectsymbols.namesakeExcited statesymbolsEmission spectrumAtomic physicsLuminescenceExcitation
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Fragmentation of polycarbonate macroinitiators in solution and in the bulk state

1990

The diphenylethane initiator 3,4-diethyl-3,4-(p-methoxyphenyl)-hexane (T–OCH3) was synthesized. By cocondensation of bisphenol A or C and the bisphenol derivative (“T”) of T–OCH3 with phosgene, polycarbonate macroinitiators PC(TxA1-x) and PC(TxC1-x) with different compositions x were made. The thermal fragmentation of T–OCH3 and the copolycarbonates was investigated with and without a radical scavenger both in solution and in the bulk state. The primary dissociation of T–OCH3 is a monomolecular Arrhenius process with a characteristic temperature of T* (τ = 1h) = 140°C (τ: average life time of the intact molecule). When the radicals are not intercepted, the dissociation is excessively revert…

Arrhenius equationPolymers and PlasticsChemistryRadicalActivation energyCondensed Matter PhysicsDissociation (chemistry)symbols.namesakeFragmentation (mass spectrometry)visual_artPolymer chemistryMaterials Chemistryvisual_art.visual_art_mediumsymbolsPhysical and Theoretical ChemistryPolycarbonateRadical disproportionationGlass transitionJournal of Polymer Science Part B: Polymer Physics
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Numerical Studies of the Diffusion Processes and First Step Oxidation in Nickel-Oxygen Systems by Variable Charge Molecular Dynamics

2010

Variable charge molecular dynamic simulations have been performed to study the diffusion mechanisms of oxygen atoms (O) in nickel (Ni) in the temperature range 950-1600 K and the very first steps of oxidation of monocrystalline nickel surfaces at 300 K and 950 K. The oxygen diffusivity can be well described by an Arrhenius law over the temperature range considered. The oxygen diffusion coefficient has been analysed and values of Ea = 1.99 eV for the activation energy and D0 = 39 cm2.s-1 for the pre-exponential factor were obtained. The first steps growth of the oxide layer show that after the dissociative chemisorption of the oxygen molecules on nickel surface, the oxidation leads to an isl…

Arrhenius equationRadiationDiffusionOxideThermodynamicschemistry.chemical_elementActivation energyAtmospheric temperature rangeIsland growthCondensed Matter PhysicsOxygensymbols.namesakechemistry.chemical_compoundNickelchemistrysymbolsPhysical chemistryGeneral Materials ScienceDefect and Diffusion Forum
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Modeling polyethylene with the bond fluctuation model

1997

This work presents an application of recently developed ideas about how to map real polymer systems onto abstract models. In our case the abstract model is the bond fluctuation model with a Monte Carlo dynamics. We study the temperature dependence of chain dimensions and of the self-diffusion behavior in the melt from high temperatures down to 200 K. The chain conformations are equilibrated over the whole temperature range, which is possible for the abstract type of model we use. The size of the chains as measured by the characteristic ratio is within 25% of experimental data. The simulated values of the chain self-diffusion coefficient have to be matched to experimental information at one …

Arrhenius equationSelf-diffusionWork (thermodynamics)ChemistryMonte Carlo methodGeneral Physics and AstronomyThermodynamicsActivation energyAtmospheric temperature rangesymbols.namesakeViscositysymbolsStatistical physicsPhysical and Theoretical ChemistryScaling
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Temperature dependance of the generation and decay of E’ centers induced in silica by 4.7eV laser radiation

2009

We report a study of the generation of silicon dangling bonds (E' centers) induced in fused silica by 4.7 eV laser irradiation in the 10 200 K the induced defects undergo a post-irradiation decay due to their reaction with mobile H(2). The interplay between generation and annealing gives rise to a bell-shaped temperature dependence of the concentration of induced E' centers, peaking at 250 K

Arrhenius equationSiliconChemistryAnnealing (metallurgy)Dangling bondchemistry.chemical_elementsilica point defectsActivation energyRadiationCondensed Matter PhysicsLaserMolecular physicsElectronic Optical and Magnetic Materialslaw.inventionsymbols.namesakeNuclear magnetic resonancelawMaterials ChemistryCeramics and CompositessymbolsIrradiationSilica laser effects annealing
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Kinetischer nachweis zweier arten von ionenpaaren bei der anionischen polymerisation von styrol in tetrahydropyran

1967

Die durch Na-Naphthalin angeregte Polymerisation des Styrols in THP wurde im Temperaturbereich von -40 bis +50°C kinctisch verfolgt. Die Geschwindigkeitskonstante kw(±) der uber das lonenpaar erfolgenden Polymerisation wurde gemessen, indem die elektrolytische Dissoziation durch Zusatz von Tetraphenylbornatrium unterdruckt wurde. Oberhalb von 20°C ergibt sich bei Auftragung nach ARRHENIUS eine Gerade, aus welcher Aktivierungsenergie Ec und Frequenzfaktor Ac des Kontaktionenpaares zu berechnen sind. Diese Parameter stimmen in guter Naherung mit den E- und A- Werten uberein, die in sehr schwach polaren Losungsmitteln fur die anionische Polymerisation erhalten werden. Unterhalb von +20°C weich…

Arrhenius equationchemistry.chemical_compoundsymbols.namesakeReaction rate constantchemistryPolymerizationPolymer chemistryEnthalpysymbolsFrequency factorActivation energyArrhenius plotStyreneDie Makromolekulare Chemie
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1981

The anionic polymerization of tert-butyl methacrylate (TBMA) in tetrahydrofuran, using Na+ and Cs+ as counterions proceeds without side reactions even at room temperature. The resulting molecular weight distributions are nearly monodisperse (Mw/Mn ⩽ 1,01). The rate constants for the propagation of ion pairs were measured in the range from + 15 to −100°C. The Arrhenius plots are linear, but different for the two counterions, resulting in the following numerical values for the frequency exponent A and the activation energy Ea: A = 8,5 and Ea = 7,2 kcal/mol = 30 kJ/mol for Na+; A = 9,5 and Ea = 5,6 kcal/mol = 23 kJ/mol for Cs+. The difference between the counterions, which is in contrast to th…

Arrhenius equationsymbols.namesakechemistry.chemical_compoundAnionic addition polymerizationReaction rate constantchemistryPolymerizationSteric factorPolymer chemistrysymbolsActivation energyMethyl methacrylateTetrahydrofuranDie Makromolekulare Chemie
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Isolation and characterization of a complement-activating lipid extracted from human atherosclerotic lesions.

1990

The major characteristics of human atherosclerotic lesions are similar to those of a chronic inflammatory reaction, namely fibrosis, mesenchymal cell proliferation, the presence of resident macrophages, and cell necrosis. Atherosclerosis exhibits in addition the feature of lipid (mainly cholesterol) accumulation. The results of the present report demonstrate that a specific cholesterol-containing lipid particle present in human atherosclerotic lesions activates the complement system to completion. Thus, lipid could represent a stimulatory factor for the inflammatory reaction, whose underlying mechanistic basis may be, at least in part, complement activation. The complement-activating lipid …

ArteriosclerosisComplement Pathway AlternativeImmunologyInflammationMuscle Smooth VascularC5-convertasechemistry.chemical_compoundMesenchymal cell proliferationmedicineHumansImmunology and AllergyComplement ActivationImmunoelectrophoresisAortaTriglyceridesCholesterolFatty AcidsComplement System ProteinsArticlesLipidsComplement systemCarotid ArteriesCholesterolchemistryBiochemistryLow-density lipoproteinChromatography GelAlternative complement pathwaylipids (amino acids peptides and proteins)Lipid particlemedicine.symptomJournal of Experimental Medicine
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Complement and atherogenesis: The unknown connection

1999

The question why low-density lipoprotein (LDL) stranded in the subendothelium of arteries should acquire the proinflammatory properties that initiate and sustain atherogenesis has puzzled researchers for decades. The most popular concept contends that oxidative processes are crucial because oxidized LDL (ox-LDL) produced in vitro has atherogenic properties and small amounts of it are found in atherosclerotic lesions. Recently, a possible role for vascular infections has also been considered because infectious agents, in particular Chlamydia pneumoniae, are sometimes present in the lesions. Here, evidence is summarized for a different concept of atherogenesis, which evolves from the fact tha…

ArteriosclerosisVascular diseaseInflammationGeneral MedicineChlamydia InfectionsChlamydophila pneumoniaeMacrophage ActivationBiologymedicine.diseaseProinflammatory cytokineLipoproteins LDLPathogenesischemistry.chemical_compoundImmune systemchemistryLow-density lipoproteinImmunologymedicineHumansMacrophagelipids (amino acids peptides and proteins)medicine.symptomComplement ActivationLipoproteinAnnals of Medicine
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The Peroxisomal 3-keto-acyl-CoA thiolase B Gene Expression Is under the Dual Control of PPARα and HNF4α in the Liver

2011

PPARα and HNF4α are nuclear receptors that control gene transcription by direct binding to specific nucleotide sequences. Using transgenic mice deficient for either PPARα or HNF4α, we show that the expression of the peroxisomal3-keto-acyl-CoA thiolase B(Thb) is under the dependence of these two transcription factors. Transactivation and gel shift experiments identified a novel PPAR response element within intron 3 of theThbgene, by which PPARα but not HNF4α transactivates. Intriguingly, we found that HNF4α enhanced PPARα/RXRα transactivation from TB PPRE3 in a DNA-binding independent manner. Coimmunoprecipitation assays supported the hypothesis that HNF4α was physically interacting with RXR…

Article SubjectResponse elementPeroxisome proliferator-activated receptorBiology03 medical and health sciencesTransactivation0302 clinical medicineDrug DiscoveryGene expression[SDV.BBM] Life Sciences [q-bio]/Biochemistry Molecular BiologySDV:BBMPharmacology (medical)[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular Biologylcsh:QH301-705.5[ SDV.BBM ] Life Sciences [q-bio]/Biochemistry Molecular BiologyTranscription factor030304 developmental biology[SDV.MHEP.EM] Life Sciences [q-bio]/Human health and pathology/Endocrinology and metabolismchemistry.chemical_classificationGeneticsEndocrinology and metabolism0303 health sciencesThiolaseIntron[ SDV.MHEP.EM ] Life Sciences [q-bio]/Human health and pathology/Endocrinology and metabolism[SDV.MHEP.EM]Life Sciences [q-bio]/Human health and pathology/Endocrinology and metabolismCell biologylcsh:Biology (General)Nuclear receptorchemistry030220 oncology & carcinogenesisEndocrinologie et métabolismeResearch ArticlePPAR Research
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