Search results for "Thermal Stability"

showing 10 items of 262 documents

X‐irradiation induced photo‐ and thermostimulated luminescence of CsCdF 3 :Mn crystals

2005

Photo- and thermostimulated luminescence (PSL and TSL respectively) of previously X-irradiated CsCdF3 crystal doped with Mn were investigated. After X-irradiation of CsCdF3 crystal at 8 K PSL bands at about 300 nm and 550 nm appear. Several stimulation bands can be revealed for luminescence at 300 nm and 550 nm. The stimulation band at 340 nm is related to an F-type centre absorption band in accordance with the Mollwo-Ivey relation for halide crystals. Subsequent heating of the crystal after X-irradiation at 8 K shows TSL peaks in the temperature regions 8 K – 90 K and 200 K – 300 K. The spectral composition of the TSL involves both bands at 300 nm and 550 nm. Experiments performed allow us…

CrystalAbsorption bandChemistryDopingAnalytical chemistryHalideThermal stabilityIrradiationLuminescenceIonphysica status solidi (c)
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Thermal stability and crystallization kinetics of Al4Mn quasicrystals as studied by exoelectron emission and DTA methods

1995

Crystallization kineticsMaterials sciencelawKineticsMetallurgyQuasicrystalThermodynamicsGeneral Materials ScienceThermal stabilityCrystallizationExoelectron emissionlaw.inventionJournal of Materials Science Letters
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Performance of a thermoelectric module based on n-type (La0.12Sr0.88)0.95TiO3-δ and p-type Ca3Co4-xO9+δ

2020

Here, we present the performance of a thermoelectric (TE) module consisting of n-type (La0.12Sr0.88)0.95TiO3 and p-type Ca3Co4-xO9+δ materials. The main challenge in this investigation was operation of TE module in different atmosphere conditions, since n-type has its optimum TE-performance at reducing, while p-type at oxidizing conditions. The TE module was exposed to two different atmospheres and demonstrated higher stability in N2 atmosphere than in air. The maximum electrical power output decreased after 40 h when the hot side was exposed to N2 at 600 °C, while only 1 h at 400 °C in ambient air was enough to oxidize (La0.12Sr0.88)0.95TiO3 followed by a reduced electrical power output. T…

DiffractionMaterials scienceSolid-state physicsAnalytical chemistryCondensed Matter PhysicsVDP::Teknologi: 500::Elektrotekniske fag: 540Electronic Optical and Magnetic MaterialsAtmosphereThermoelectric generatorThermoelectric effectOxidizing agentMaterials ChemistryThermal stabilityElectric powerElectrical and Electronic Engineering
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Triphenylmethyl and triphenylsilyl based molecular glasses for photonic applications

2015

Triphenylmethyl and triphenylsilyl structural fragments can be used to obtain glass forming, solution processable materials from polar chromophore molecules. Large number of compounds has been synthesized taking advantage of this approach, making it possible to identify some structure-property relations. Regarding the non-linear optical (NLO) properties of the given materials it is evident that triphenylmethyl groups help shielding unwanted NLO efficiency limiting dipolar interactions between polar chromophores in solid films. Chromophore stacking is still observed for compounds with large dipole momentum values. The glass transition temperatures of the compounds increase with the molecular…

DipoleOpticsMaterials sciencebusiness.industryStackingMoleculePolarPhysical chemistryNonlinear opticsThermal stabilityChromophorebusinessGlass transitionSPIE Proceedings
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Comparative Study of the Mechanical Unfolding Pathways of α- and β-Peptides

2015

Using molecular simulations, we analyze the unfolding pathways of various peptides. We compare the mechanical unfolding of a β-alanine's octamer (β-HAla8) and an α-alanine's decamer (α-Ala10). Using force-probe molecular-dynamics simulations, to induce unfolding, we show that the 3(14)-helix formed by β-HAla8 is mechanically more stable than the α-helix formed by α-Ala10, although both structures are stabilized by six hydrogen bonds. Additionally, computations of the potential of mean force validate this result and show that also the thermal stability of the 3(14)-helix is higher. It is demonstrated that β-HAla8 unfolds in a two-step fashion with a stable intermediate. This is contrasted wi…

Dynamic strengthHydrogen bondHydrogen BondingMolecular Dynamics SimulationProtein Structure SecondarySurfaces Coatings and Filmschemistry.chemical_compoundCrystallographyMonomerchemistrybeta-AlanineMaterials ChemistryBiophysicsThermal stabilityHistone octamerPhysical and Theoretical ChemistryPotential of mean forcePeptidesThe Journal of Physical Chemistry B
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Thermal analysis as a quality tool for assessing the influence of thermo-mechanical degradation on recycled poly(ethylene terephthalate)

2009

Mechanical recycling of poly(ethylene terephthalate) (PET) was simulated by multiple processing to assess the effects of thermo-mechanical degradation, and characterized using rheological and thermal analysis techniques. Thermo-mechanical degradation under repeated extrusion induces chain scission reactions in PET, which result in a dramatic loss in the deformation capabilities and an increase in the fluidity of the polymer under reprocessing, reducing its recycling possibilities after four extrusion cycles. Multiple reprocessing severely affects the storage modulus and the microstructure of recycled PET, both in the amorphous and crystalline regions. Multimodal melting behavior is observed…

EthyleneMaterials scienceSolucions polimèriquesPolymers and PlasticsOrganic ChemistryTermoplàsticschemistry.chemical_compoundCrystallinityThermchemistryDegradation (geology)ExtrusionThermal stabilityComposite materialThermal analysisMelt flow index
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2-(N,N-Diethylaminomethyl)-6,7-trihydroquinolinyl-8-ylideneamine-Ni(ii) chlorides: application in ethylene dimerization and trimerization

2020

A series of Ni(II) complexes with the general formula [2-((NEt2)Me)-8-{N(Ar)}C9H8N]NiCl2, where Ar = 2,6-Me2C6H3 in Ni1, 2,6-Et2C6H3 in Ni2, 2,6-i-Pr2C6H3 in Ni3, 2,4,6-Me3C6H2 in Ni4, 2,6-Et2-4-MeC6H2 in Ni5, and 2,4,6-t-Bu3C6H2 in Ni6, has been prepared using a one-pot reaction of 2-(N,N-diethylaminomethyl)-6,7-dihydroquinolin-8(5H)-one with the corresponding aniline and nickel dichloride hexahydrate. The resultant complexes were characterized using elemental analysis and FT-IR spectroscopy, while the mononuclear Ni1 and Ni3 were also the subject of single-crystal X-ray diffraction study. On activation with MMAO, the complexes Ni1–Ni6 displayed good activity in ethylene oligomerization, f…

EthyleneNickel metallographyInduction periodAliphatic compoundsGeneral ChemistryBinary alloysMedicinal chemistryChlorine compoundsCatalysisCatalysisCatalyst selectivityAnilineEthylenechemistry.chemical_compoundAnilinechemistryElemental analysisCatalyst activityMaterials ChemistrySingle crystalsThermal stabilitySelectivitySpectroscopyDimerizationNew Journal of Chemistry
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Structural stability and properties of three isoforms of the major light-harvesting chlorophyll a/b complexes of photosystem II.

2008

AbstractThree isoforms of the major light-harvesting chlorophyll (Chl) a/b complexs of photosystem II (LHCIIb) in the pea, namely, Lhcb1, Lhcb2, and Lhcb3, were obtained by overexpression of apoprotein in Escherichia coli and by successfully refolding these isoforms with thylakoid pigments in vitro. The sequences of the protein, pigment stoichiometries, spectroscopic characteristics, thermo- and photostabilities of different isoforms were analysed. Comparison of their spectroscopic properties and structural stabilities revealed that Lhcb3 differed strongly from Lhcb1 and Lhcb2 in both respects. It showed the lowest Qy transition energy, with its reddest absorption about 2 nm red-shifted, an…

Gene isoformChlorophyllChlorophyll aProtein FoldingPhotosystem IIBiophysicsLight-Harvesting Protein ComplexesPhotochemistryBiochemistryThylakoidsReconstitutionchemistry.chemical_compoundPigmentPigment stoichiometryEscherichia coliThermal stabilityMajor light-harvesting chlorophyll a/b complex of photosystem IIProtein Structure QuaternaryThermostabilityPlant ProteinsChlorophyll APeasPhotosystem II Protein ComplexCell BiologyRecombinant ProteinsIsoenzymeschemistryPhotostabilityChlorophyllThylakoidvisual_artBiophysicsvisual_art.visual_art_mediumThermostabilityBiochimica et biophysica acta
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Isolation of the CH3˙ rotor in a thermally stable inert matrix: first characterization of the gradual transition from classical to quantum behaviour …

2014

International audience; Matrix isolation is a method which plays a key role in isolating and characterizing highly reactive molecularradicals. However, the isolation matrices, usually composed of noble gases or small diamagnetic molecules,are stable only at very low temperatures, as they begin to desegregate even above a few tens of Kelvin.Here we report on the successful isolation of CH3 radicals in the cages of a nearly inert clathrate–SiO2matrix. This host is found to exhibit a comparable inertness with respect to that of most conventionalnoble gas matrices but it is characterized by a peculiar thermal stability. The latter property is related to thecovalent nature of the host material a…

General Physics and Astronomy02 engineering and technology01 natural sciences7. Clean energylaw.inventionMatrix (mathematics)CH3 methyl radicals EPR clathrate sio2 melanophlogitelawComputational chemistry0103 physical sciencesMoleculeThermal stabilityPhysical and Theoretical ChemistryElectron paramagnetic resonanceQuantumdefects010304 chemical physicsChemistryMatrix isolationNoble gas[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyChemical physicsDiamagnetismEPR0210 nano-technology
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New approach for synthesis of poly(ethylglyoxylate) using Maghnite-H + , an Algerian proton exchanged montmorillonite clay, as an eco-catalyst

2017

International audience; In this works, we have explored a new method for a green synthesis of poly(ethylglyoxylate) (PEtG). This method consists on using a montmorillonite clay called Maghnite-H+ as an eco-catalyst to replace triethylamine which is toxic. Cationic polymerization experiments are performed in bulk conditions at three temperatures (-40 degrees C, 25 degrees C, 80 degrees C) and in THF solutions at room temperature (25 degrees C). At 25 degrees C, an optimum ratio of 5 wt% of catalyst leads to molar masses up to 22000 g/mol in THF solutions. Polymerizations in bulk conditions lead to slightly lower masses than experiments conducted in THF solutions. However, bulk polymerization…

Green chemistryThermogravimetric analysisMaterials scienceepsilon-caprolactonePolymers and PlasticsBulk polymerizationMaghnite-H+ring-opening polymerization02 engineering and technologyEthylglyoxylate010402 general chemistry7. Clean energy01 natural sciencesalcoholschemistry.chemical_compoundbiodegradable plasticsMaterials Chemistrycationic polymerizationionic polymerizationsThermal stabilityComposite materialsheet silicatespoly(methyl glyoxylate)degradationchemistry.chemical_classificationMolar masscopolymergreen chemistrybis-macromonomersCationic polymerizationbiodegradable polymerGeneral ChemistryPolymer021001 nanoscience & nanotechnology0104 chemical sciences[ CHIM.POLY ] Chemical Sciences/PolymersMontmorillonite[CHIM.POLY]Chemical Sciences/PolymersChemical engineeringchemistryCeramics and Compositeseco-catalyst0210 nano-technology
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