Search results for "neutron diffraction"

showing 10 items of 102 documents

Molecular origin and hydration dependence of protein anharmonicity: an elastic neutron scattering study.

2010

Two main onsets of anharmonicity are present in protein dynamics. Neutron scattering on protein hydrated powders revealed a first onset at about 150 K and a second one at about 230 K (the so called dynamical transition). In order to assess the molecular origin of protein anharmonicity, we study different homomeric polypeptides by incoherent elastic neutron scattering, thus disentangling the contribution of different molecular groups in proteins. We show that methyl group rotations are the main contributors to the low temperature onset. Concerning the dynamical transition, we show that it also occurs in absence of side chains; however, the presence and mobility of side chains substantially i…

Elastic scatteringQuantitative Biology::BiomoleculespolypeptideTransition temperatureProtein dynamicsAnharmonicitymean square displacementsTemperatureGeneral Physics and AstronomyProteinsWaterNeutron scatteringElasticitychemistry.chemical_compoundCrystallographyNeutron DiffractionAmplitudechemistryChemical physicsprotein dynamicSide chainPhysics::Chemical PhysicsPhysical and Theoretical ChemistryPeptidesMethyl groupPhysical chemistry chemical physics : PCCP
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A new calcium sulfate hemi-hydrate

2010

Calcium sulfate hydrates receive significant attention due to numerous large scale industrial applications. There has been a long debate on the possible existence of two gypsum hemi-hydrate polymorphs, denoted alpha- and beta-CaSO(4).0.5H(2)O. In this work, a new crystal structure of calcium sulfate hemi-hydrates is presented, denoted beta-CaSO(4).0.5H(2)O. The structure was solved using powder neutron diffraction data, the space group is P3(1) and the unit cell in a hexagonal setting a = 6.9268(1), c = 12.7565(3) A. The structure has two calcium-oxygen coordination polyhedra: Ca1 is eight coordinated and has Ca-O bond lengths in the range 2.31(3) to 2.89(2) A and Ca2 is nine coordinated an…

GypsumHydrogen bondNeutron diffractionCrystal structureengineering.materialInorganic ChemistryBond lengthCrystallographychemistry.chemical_compoundchemistryengineeringMoleculeSulfateHydrate
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Heptane Adsorption in Silicalite-1: Neutron Scattering Investigation

2007

International audience; Structural properties of confined deuterated n-heptane in silicalite-1 have been investigated by neutron scattering experiments during the adsorption process. At 300 K, the adsorption isotherm shows a sharp inflection at a loading near Nads ) 4 molecules per silicalite-1 unit cell. In addition, the diffusivities obtained from recent QENS data exhibit a loading dependence. Our motivation is to find structural signatures of the peculiar behavior of n-heptane in silicalite-1 and to check the numerous computer simulation findings of this behavior. Our detailed neutron diffraction investigation agrees with the MONO-ORTHO phase transition of the silicalite-1 above a Nads v…

HeptanePhase transitionChemistryRietveld refinementNeutron diffractionThermodynamics02 engineering and technologyNeutron scattering010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materials[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry.chemical_compoundCrystallography[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistryGeneral EnergyAdsorptionDeuterium[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryMoleculePhysical and Theoretical Chemistry0210 nano-technology
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The solubilisation behaviour of some dichloroalkanes in aqueous solutions of PEO-PPO-PEO triblock copolymers: a dynamic light scattering, fluorescenc…

2006

The aggregation behaviour of PEO-PPO-PEO triblock copolymers in water and in water + chlorinated additive mixtures was studied by means of fluorescence spectroscopy, dynamic light scattering (DLS), and small-angle neutron scattering (SANS). The copolymers were chosen such as to investigate the effects of molecular architecture (L35 and 10R5) and molecular weight by keeping constant the hydrophilic/hydrophobic balance (F88 and F108). 1,2-Dichloroethane was used as a prototype of water basins contaminants. The hydrodynamic radius of the block copolymer aggregates (R(h,M)) and the intensity ratio of pyrene of the first and the third vibrational band (I(1)/I(3)) were determined as a function of…

Hydrodynamic radiusAnalytical chemistryGeneral Physics and AstronomyMICELLIZATIONNeutron scatteringPHASE-BEHAVIORFluorescence spectroscopyPolyethylene GlycolsDynamic light scattering:OSCILLATORY SHEAR MEASUREMENTSBLOCK-COPOLYMERAlkanesCopolymerOrganic chemistryMOLAR VOLUMESSURFACTANTSPhysical and Theoretical ChemistrySolubilityTEMPERATUREAqueous solutionChemistryWaterSmall-angle neutron scatteringSolutionsMICELLAR STRUCTURENeutron DiffractionRefractometrySpectrometry FluorescenceSolubilityWATER-OIL SYSTEMSPropylene GlycolsTHERMODYNAMIC PROPERTIESChlorinePhysical chemistry chemical physics : PCCP
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Hydration dependent dynamics in sol-gel encapsulated myoglobin.

2008

In this work we study the effect of hydration on the dynamics of a protein in confined geometry, i.e. encapsulated in a porous silica matrix. Using elastic neutron scattering we investigate the temperature dependence of the mean square displacements of non-exchangeable hydrogen atoms of sol-gel encapsulated met-myoglobin. The study is extended to samples at 0.2, 0.3 and 0.5 g water/g protein fractions and comparison is made with met-myoglobin powders at the same average hydration and with a dry powder sample. Elastic data are analysed using a model of dynamical heterogeneity to take into account deviations of elastic intensity from gaussian behaviour in a large momentum transfer range and r…

HydrogenBiophysicsHydrationchemistry.chemical_elementSol–gelNeutron scatteringELASTIC NEUTRON-SCATTERINGPROTEIN HYDRATIONAnimalsDynamical heterogeneityPorositySol-gelSPECTROSCOPYMyoglobinProtein dynamicsSolvent dynamicMomentum transferTemperatureWaterGeneral MedicineElasticityCrystallographyNeutron DiffractionSolvation shellchemistryChemical physicsProtein dynamicSilica hydrogelsGelsTRANSITIONHydrogenEuropean biophysics journal : EBJ
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Neutron Diffraction Study of the in Situ Oxidation of UO2

2009

This paper discusses uranium oxide crystal structure modifications that are observed during the low-temperature oxidation which transforms UO(2) into U(3)O(8). The symmetries and the structural parameters of UO(2), beta-U(4)O(9), beta-U(3)O(7), and U(3)O(8) were determined by refining neutron diffraction patterns on pure single-phase samples. Neutron diffraction patterns were also collected during the in situ oxidation of powder samples at 483 K. The lattice parameters and relative ratios of the four pure phases were measured during the progression of the isothermal oxidation. The transformation of UO(2) into U(3)O(8) involves a complex modification of the oxygen sublattice and the onset of…

In situKineticsNeutron diffractionchemistry.chemical_element02 engineering and technologyCrystal structure[CHIM.MATE]Chemical Sciences/Material chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesOxygenIsothermal process0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistry[ CHIM.MATE ] Chemical Sciences/Material chemistryLattice (order)Physical chemistryUranium oxidePhysical and Theoretical Chemistry0210 nano-technology
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ChemInform Abstract: Neutron Diffraction Study of the in situ Oxidation of UO2.

2009

This paper discusses uranium oxide crystal structure modifications that are observed during the low-temperature oxidation which transforms UO2 into U3O8. The symmetries and the structural parameters of UO2, β-U4O9, β-U3O7, and U3O8 were determined by refining neutron diffraction patterns on pure single-phase samples. Neutron diffraction patterns were also collected during the in situ oxidation of powder samples at 483 K. The lattice parameters and relative ratios of the four pure phases were measured during the progression of the isothermal oxidation. The transformation of UO2 into U3O8 involves a complex modification of the oxygen sublattice and the onset of complex superstructures for U4O…

In situchemistry.chemical_compoundChemistryLattice (order)KineticsNeutron diffractionUranium oxidePhysical chemistrychemistry.chemical_elementGeneral MedicineCrystal structureOxygenIsothermal processChemInform
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Two stage magnetic ordering and spin idle behavior of the coordination polymer Co3(OH)2(C4O4)2·3H2O determined using neutron diffraction.

2011

We report the magnetic structure of two of the magnetically ordered phases of Co(3)(OH)(2)(C(4)O(4))(2)·3H(2)O, a coordination polymer that consists of a triangular framework decorated with anisotropic Co(II) ions. The combination of neutron diffraction experiments and magnetic susceptibility data allows us to identify one phase as displaying spin idle behavior, where only a fraction of the moments order at intermediate temperatures, while at the lowest temperatures the system orders fully. This novel magnetic behavior is discussed within the framework of a simple Hamiltonian and representational analysis and rationalizes this multiphase behavior by considering the combination of frustratio…

Inorganic ChemistryIdlechemistry.chemical_compoundCondensed matter physicsMagnetic structureChemistryCoordination polymerNeutron diffractionPhysical and Theoretical ChemistryAnisotropyInorganic chemistry
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A microcalorimetric study of the different states of argon and nitrogen adsorbed AT 77 K on silicalite-I and ZSM-5

1992

The adsorption of argon and nitrogen on a series of MFI-type zeolites (silicalite-I (Si/Al>1000) and HZSM-5 (16<Si/Al<120)) was studied by isothermal microcalorimetry, volumetry and neutron diffraction.

Isothermal microcalorimetryAdsorptionArgonchemistryNeutron diffractionInorganic chemistryAnalytical chemistrychemistry.chemical_elementZSM-5ZeoliteMolecular sieveNitrogenJournal of Thermal Analysis
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Magnetic and structural properties of the double-perovskite Ca2FeReO6

2002

Abstract We suceeded in the preparation of polycrystalline Ca2FeReO6 which has a Curie temperature TC of 540 K, the highest value of all magnetic perovskites investigated till now. This material has been characterised by X-ray and neutron powder diffraction. We found at 548 K, a monoclinic unit cell (space group P21/n) with a=5.4366(5) A , b=5.5393(5) A , c=7.7344(5) A , and β=90.044(4)°. For temperatures below 400 K, a phase separation in two monoclinic phases with identical cell volume is observed in neutron scattering. The two phases possess different magnetic structure and coercivity. The conductivity is thermally activated for all temperatures and no significant magnetoresistivity is o…

Magnetic structureChemistryNeutron diffractionSpace groupGeneral ChemistryNeutron scatteringCoercivityCondensed Matter PhysicsCrystallographyMaterials ChemistryCurie temperatureCrystalliteMonoclinic crystal systemNuclear chemistrySolid State Communications
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