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showing 10 items of 1808 documents

The structure, phase transition and molecular dynamics of [C(NH2)3]3[Sb2Br9]

2005

The crystal structures of [C(NH2)3]3[Sb2Br9] (Gu3Sb2Br9) at 300 K and of [C(NH2)3]3[Sb2Cl9] (Gu3Sb2Cl9) at 90 and 300 K are determined. The compounds crystallize in the monoclinic space group: C 2/c. The structure is composed of Sb2X93− (X = Cl, Br) ions, which form two-dimensional layers through the crystal, and guanidinium cations. In Gu3Sb2Br9 the structural phase transformation of the first-order type is detected at 435/450 K (on cooling/heating) by the DSC and dilatometric techniques. The dielectric relaxation process in the frequency range between 75 kHz and 5 MHz over the low temperature phase indicates reorientations of weakly distorted guanidinium cations. The proton 1H NMR second-…

CrystalPhase transitionCrystallographyDifferential scanning calorimetryChemistryStereochemistryPhase (matter)Space groupGeneral Materials ScienceDielectricCrystal structureCondensed Matter PhysicsMonoclinic crystal systemJournal of Physics: Condensed Matter
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Crystal structure, phase transition and ferroelectric properties of the [(CH3)3NH]3[Sb2Cl9(1 x)Br9x] (TMACBA) mixed crystals

2003

The paraelectric–ferroelectric phase transition in the [(CH3)3NH]3[Sb2Cl9(1−x) Br9x] (TMACBA) mixed crystals is investigated by the differential scanning calorimetry, dilatometric and dielectric methods. The phase transition is found at 363.5, 362.7, 360.5 and 350.9 K (on cooling) for TMACBA crystals with x = 0, 0.02, 0.17 and 0.42, respectively. The crystal structures of the pure bromine analogue (x = 1), TMABA, and the mixed crystal TMACBA (x = 0.55) are determined at 297 K. TMABA crystallizes in the trigonal space group Rc: a = 15.098(2) A, c = 21.906(4) A, Z = 3, R1 = 0.0393, wR2 = 0.0746. Its structure is built up of discrete Sb2Br93− bioctahedra and disordered trimethylammonium cation…

CrystalPhase transitionCrystallographyDifferential scanning calorimetryStereochemistryChemistryPhase (matter)General Materials ScienceDielectricCrystal structureCondensed Matter PhysicsFerroelectricityMonoclinic crystal systemJournal of Physics: Condensed Matter
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Structure, phase transitions and molecular motions in ferroelastic (C4H8NH2)SbCl6·(C4H8NH2)Cl

2002

The crystal structure at 293 K of the new pyrrolidinium chloroantimonate (V) analogue, (C4H8NH2)SbCl6(C4H8NH2)Cl, has been determined by x-ray diffraction as monoclinic, space group P21/c, Z = 8. The crystal is built up of isolated SbCl6- anions, two types of inequivalent pyrrolidinium cation and isolated Cl- ions. It undergoes five solid-solid phase transitions: at 351/374 K of first-order type (cooling/heating, respectively), at 356 and 152 K second order and at 135/141 and 105/134 K first order, detected by differential scanning calorimetry, dilatometric and dielectric measurements. The ferroelastic domain structure appears between 152 and 135 K. The proton nuclear magnetic resonance sec…

CrystalPhase transitionCrystallographyFerroelasticityDifferential scanning calorimetryChemistryRelaxation (NMR)Spin–lattice relaxationGeneral Materials ScienceCrystal structureCondensed Matter PhysicsMonoclinic crystal systemJournal of Physics: Condensed Matter
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Structure and phase transitions in the ferroelastic [C(NH2)3]3Bi2Br9crystal

1999

Differential scanning calorimetry, dilatometric, dielectric and linear birefringence measurements have been used to study the ferroelastic [C(NH2)3]3Bi2Br9 crystal. The x-ray studies showed that it crystallizes at room temperature in the monoclinic symmetry, space group P21/m. The crystal undergoes a complex sequence of phase transitions: at 311 K, 333.5 K, 350 K, 415 K and 425 K. All phase transitions were found to be of first order type. The ferroelastic domain structure is maintained from room temperature up to 425 K. The temperature measurements of the linear birefringence and optical observations suggest the tetragonal symmetry of the parent paraelastic phase above 425 K.

CrystalPhase transitionCrystallographyTetragonal crystal systemDifferential scanning calorimetryBirefringenceChemistryPhase (matter)General Materials ScienceDielectricCrystal structureCondensed Matter PhysicsJournal of Physics: Condensed Matter
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Protective Effects of L- and D-Carnosine on R-Crystallin Amyloid Fibril Formation: Implications for Cataract Disease

2009

Mildly denaturing conditions induce bovine ?-crystallin, the major structural lens protein, to self-assemble into fibrillar structures in vitro. The natural dipeptide L-carnosine has been shown to have potential protective and therapeutic significance in many diseases. Carnosine derivatives have been proposed as potent agents for ophthalmic therapies of senile cataracts and diabetic ocular complications. Here we report the inhibitory effect induced by the peptide (L- and D-enantiomeric form) on ?-crystallin fibrillation and the almost complete restoration of the chaperone activity lost after denaturant and/or heat stress. Scanning force microscopy (SFM), thioflavin T, and a turbidimetry ass…

CrystallinCircular dichroismAmyloidCarnosinePeptideMicroscopy Atomic ForceBiochemistryCataractLens proteinRats Sprague-Dawleychemistry.chemical_compoundOrgan Culture TechniquesCrystallinChaperone activityAnimalsalpha-CrystallinsSFM Scanning Force Microscopychemistry.chemical_classificationDipeptideCD Circular DichroismThT Thioflavin TCalorimetry Differential ScanningDSC Differential Scanning CalorimetryCircular DichroismCarnosineStereoisomerismIn vitroeye diseasesRatsSpectrometry FluorescencechemistryBiochemistryHEPES 4-(2-Hydroxyethyl)piperazine-1-ethanesulfonic acidThioflavinCattleFemaleSpectrophotometry Ultravioletsense organsAmyloid fibrilMolecular Chaperones
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Study of the MOCVD growth of ZnO on GaAs substrates: Influence of the molar ratio of the precursors on structural and morphological properties

2007

Abstract ZnO thin films were grown by metal-organic chemical vapour deposition (MOCVD) on GaAs(100) and GaAs(111)A substrates. The growth experiments were performed at temperatures ranging from 290 to 500 ∘C and atmospheric pressure. Diethylzinc (DEZn) and tertiary butanol (tBuOH) were used as Zn and O precursors, respectively. The crystallinity of the grown films was studied by X-Ray Diffraction (XRD) and the thickness and morphology were investigated by Scanning Electron Microscopy (SEM). The influence of substrate orientation and molar ratio of the precursors on the crystalline orientation and morphology of the ZnO grown films was analysed.

CrystallinityMorphology (linguistics)Materials scienceAtmospheric pressureChemical engineeringScanning electron microscopeGeneral Materials ScienceSubstrate (electronics)Chemical vapor depositionMetalorganic vapour phase epitaxyElectrical and Electronic EngineeringThin filmCondensed Matter PhysicsSuperlattices and Microstructures
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Indication of an order-order-transition by a partial disordering in ABC-triblock copolymers

1996

Poly(ethylene-alt-propylene)-block-polyethylethylene-block-polystyrene (PEP-b-PEE-b-PS) triblock copolymers were synthesized by anionic polymerization and subsequent hydrogenation of poly-1,4-isoprene-block-poly-1,2-butadiene-block-polystyrene triblock copolymers (1,4PI-b-1,2PB-b-PS). Differential scanning calorimetry and dynamic mechanical spectroscopy reveal an order-order transition which is induced by the mixing of PEP and PEE above their respective order-disorder transition (ODT).

CrystallographyDifferential scanning calorimetryAnionic addition polymerizationMaterials sciencePolymers and PlasticsThermal transitionPolymer chemistryMaterials ChemistryCopolymerGeneral ChemistryDynamic mechanical analysisCondensed Matter PhysicsPolymer Bulletin
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Synthesis of Areno-Condensed [24]Annulenes

2001

[24]Annulenes condensed with three phenanthrene units (11a−d) or with three chrysene ring systems (22) were prepared by multi-step syntheses. The cyclic condensation reaction in the final step led to highly symmetrical compounds. Long flexible alkoxy groups attached to the periphery enhance the solubility and give rise to a strong aggregation of the molecules which was observed in solution by NMR and fluorescence excitation spectroscopy, and in the pure state by the detection of liquid crystalline phases in differential scanning calorimetry and polarization microscopy.

CrystallographyDifferential scanning calorimetryLiquid crystalChemistryOrganic ChemistryAlkoxy groupMoleculePhysical and Theoretical ChemistrySolubilityAnnuleneCondensation reactionRing (chemistry)PhotochemistryEuropean Journal of Organic Chemistry
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Microstructural evolution of mullites produced from single-phase gels

2007

The crystalline microstructure of mullites obtained by heating monophasic gels has been investigated. Gels with alumina to silica molar ratio of 3:2 (as in secondary mullite) and 2:1 (as in primary mullite) were prepared by gelling mixtures of aluminium nitrate and tetraethylorthosilicate. Phase transformations were induced by heating the gel precursors, with different final treatment temperatures between 1173 and 1873 K. The mullites formed as a result of thermal treatment were studied by means of X-ray diffraction, scanning electron microscopy and transmission electron microscopy. The crystalline structure (unit-cell parameters) and microstructure were determined from X-ray diffraction pa…

CrystallographyMaterials scienceChemical engineeringTransmission electron microscopyScanning electron microscopePhase (matter)NucleationMulliteThermal treatmentCrystalliteMicrostructureGeneral Biochemistry Genetics and Molecular BiologyJournal of Applied Crystallography
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Deposition of Cu Nanoparticles on the Surface of Metallic Aluminum

2012

Deposition of Cu particles by electrolysis at constant electrode potential and by internal electrolysis methods was investigated. The composition of deposited material was confirmed by optical and scanning electron microscope methods. Combination of electrolysis at constant electrode potential with internal electrolysis method was found most effective for fabrication of nanoparticle arrays. Single crystalline Cu particles are fabricated by internal electrolysis, while polycrystalline ones obtained by combined chronopotentiometric and internal electrolysis methods. The formation mechanism of Cu nanoparticles is described.

Cu nanoparticlesElectrolysisFabricationMaterials scienceChemical engineeringlawScanning electron microscopeAnalytical chemistryNanoparticleCrystalliteDeposition (law)law.inventionElectrode potentialIOP Conference Series: Materials Science and Engineering
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