Search results for "Stability"

showing 10 items of 3085 documents

The Role of Eucalyptus Species on the Structural and Thermal Performance of Cellulose Nanocrystals (CNCs) Isolated by Acid Hydrolysis

2022

Cellulose nanocrystals (CNCs) are attractive materials due to their renewable nature, high surface-to-volume ratio, crystallinity, biodegradability, anisotropic performance, or available hydroxyl groups. However, their source and obtaining pathway determine their subsequent performance. This work evaluates cellulose nanocrystals (CNCs) obtained from four different eucalyptus species by acid hydrolysis, i.e., E. benthamii, E. globulus, E. smithii, and the hybrid En × Eg. During preparation, CNCs incorporated sulphate groups to their structures, which highlighted dissimilar reactivities, as given by the calculated sulphate index (0.21, 0.97, 0.73 and 0.85, respectively). Although the impact o…

Solucions polimèriquesQD241-441cellulose nanocrystals (CNC); eucalyptus; crystallinity; thermal stability; kinetic analysiseucalyptusPolymers and Plasticskinetic analysisOrganic chemistryCristallsGeneral Chemistrycellulose nanocrystals (CNC)Materialscrystallinitythermal stabilityPolymers
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Advances in the investigation of dioxouranium(VI) complexes of interest for natural fluids

2012

Abstract The interactions of dioxouranium(VI) cation with different organic and inorganic ligands of environmental and biological interest were carefully examined with the aim to draw a chemical speciation picture of this ion in natural aquatic ecosystems and in biological fluids. Since UO22+ ion shows a significant tendency to hydrolyze, particular attention was paid in considering the hydrolysis species formation both in the presence and in absence of ligands. The results reported in the literature show that formation of the hydrolytic species assumes a great importance in the complexation models for all the UO22+-ligand systems considered. In particular, the following ligands have been t…

SpeciationDioxouranium(VI) complexes; Aqueous solutions; Inorganic ligands; Organic ligands; Speciation; SequestrationOrganic ligandsInorganic Chemistrychemistry.chemical_compoundComputational chemistryMaterials ChemistryAqueous solutionDioxouranium(VI) complexesOrganic chemistryMoleculeSettore CHIM/01 - Chimica AnaliticaCarboxylatePhysical and Theoretical ChemistryBinding siteAqueous solutionsDioxouranium(VI) complexechemistry.chemical_classificationInorganic ligandsAqueous solutionLigandSequestrationInorganic ligandUranylAmino acidchemistryOrganic ligandChemical stabilityCoordination Chemistry Reviews
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Interaction of UO2(2+) with ATP in aqueous ionic media.

2005

Interaction of dioxouranium(VI) (uranyl) ion with ATP was studied by ligand/proton and metal/hydroxide displacement technique, at very low ionic strength and at I=0.15 mol L(-1), in aqueous Me4NCl and NaCl solutions, at t=25 degrees C. Measurements were carried out in the pH range 3-8.5, before the formation of precipitate. Computer analysis allowed us to find the quite stable species UO2(ATP)H2(0), UO2(ATP)H-, UO2(ATP)2-, UO2(ATP)2(6-), UO2(ATP)2H2(4-) and UO2(ATP)(OH)3- whose formation constants are (at I=0 mol L(-1)) logbeta(112)=18.21, logbeta(111)=14.70, logbeta(110)=9.14, logbeta(120)=12.84, logbeta(122)=24.82, and logbeta(11-1)=2.09, respectively. Different values were obtained in th…

SpeciationInorganic chemistryIonic mediaBiophysicsIonic bondingLigandsBiochemistryComplexeIonMetalchemistry.chemical_compoundAdenosine TriphosphateMetals HeavySettore CHIM/01 - Chimica AnaliticaAqueous solutionLigandHydrolysisOrganic ChemistryWaterHydrogen-Ion ConcentrationUranylUranium CompoundsDioxouranium(VI)ATPchemistryStability constants of complexesvisual_artDependence on medium of stability constantvisual_art.visual_art_mediumHydroxideBiophysical chemistry
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Competing Phases Involving Spin-State and Ligand Structural Orderings in a Multistable Two-Dimensional Spin Crossover Coordination Polymer

2017

[EN] Competition between spin-crossover and structural ligand ordering is identified as responsible for multistability and generation of six different phases in a rigid two-dimensional coordination polymer formulated {Fe-II[Hg-II(SCN)(3)](2) mu-(4,4'-bipy)(2)}(n) (1) (4,4'-bipy = 4,4'-bipyridine). The structure of 1 consists of infinite linear [Fe(mu-4,4'-bipy)](n)(2n+) chains linked by in situ formed {[Hg-II(SCN)(3)](2)(mu-4,4'-bipy)}(2n-) anionic dimers. The thermal dependence of the high-spin fraction, his, features four magnetic phases defined by steps following the sequence gamma(HS) = 1 (phase 1) gamma(HS) = 1/2 (phase 2) gamma(HS) approximate to 1/3 (phase 3) gamma(HS) = 0 (phase 4) …

Spin statesCondensed matter physics010405 organic chemistryLigandChemistryCoordination polymerSpontaneous symmetry breakingGeneral Chemistry010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical scienceschemistry.chemical_compoundCrystallographySpin crossoverFISICA APLICADAPhase (matter)[PHYS.COND.CM-MS]Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]General Materials ScienceSingle crystalMultistabilityCrystal Growth & Design
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Correlations of the distribution of spin states in spin crossover compounds

1999

Abstract Short range correlations of the distribution of high spin (HS) and low spin (LS) states show up in thermal spin transition curves, decay curves of the light induced metastable HS state (LIESST state), and in structural features during the spin transitions. Correlations are due to short range interactions between the spin crossover molecules. Short range interactions may compete with omnipresent long range interactions and give rise to interesting spin transition phenomena. In this paper, the effect of correlations on the thermal spin transition in the mixed crystal system [Fe x Zn 1− x (pic) 3 ]Cl 2 ·EtOH (pic=picolylamine) is discussed. In particular the step in the thermal transi…

Spin statesCondensed matter physicsChemistrySpin transitionSpin crossoverLIESSTCorrelationInorganic ChemistrySpin crossoverLattice (order)Metastabilityddc:540Materials ChemistryMoleculeOrthorhombic crystal systemCondensed Matter::Strongly Correlated ElectronsPhysical and Theoretical ChemistryPhase transition
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Pressure-Induced High Spin State in [Fe(btr)2(NCS)2]·H2O (btr = 4,4′-bis-1,2,4-triazole)

2000

Application of hydrostatic pressure (≤ 10.5 kbar) on the two-dimensional spin transition compound [Fe(btr)2(NCS)2]·H2O (btr = 4,4‘-bis-1,2,4-triazole) results in an unexpected stabilization of the HS state. On release of the pressure, the HS state is found to be partially trapped. After thermal relaxation of the metastable HS state obtained by the LIESST effect (light-induced excited spin state trapping), a pure LS state is obtained in contrast to the pressure experiments. This different behavior supports a structural phase transition as the likely basis of the pressure-induced HS state.

Spin statesCondensed matter physicsHydrostatic pressureSpin transition124-TriazoleTrappingLIESSTSurfaces Coatings and Filmschemistry.chemical_compoundCrystallographychemistryExcited stateMetastabilityMaterials ChemistryPhysical and Theoretical Chemistry
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A spin transition molecular material with a wide bistability domain.

2002

International audience; [Fe(hyptrz)3](4-chloro-3-nitrophenylsulfonate)22 H2O (1; hyptrz=4-(3-hydroxypropyl)-1,2,4-triazole) has been synthesized and its physical properties have been investigated by several physical techniques including magnetic susceptibility measurements, calorimetry, and Mössbauer, optical, and EXAFS spectroscopy. Compound 1 exhibits a spin transition below room temperature, together with a very wide thermal hysteresis of about 50 K. This represents the widest hysteresis loop ever observed for an FeII-1,2,4-triazole spin transition material. The cooperativity is discussed on the basis of temperature-dependent EXAFS studies and of the structural features of a CuII analogu…

Spin statesExtended X-ray absorption fine structureBistabilityChemistryIronOrganic ChemistrySpin transitionChain structuresGeneral ChemistryCalorimetryEXAFS spectroscopy[CHIM.MATE]Chemical Sciences/Material chemistrySpin crossoverMagnetic susceptibilityCatalysis3. Good healthCrystallographyChemical physicsSpin crossoverMössbauer spectroscopy4-triazole
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Kinetics of phase separation in thin films: simulations for the diffusive case.

2005

We study the diffusion-driven kinetics of phase separation of a symmetric binary mixture (AB), confined in a thin-film geometry between two parallel walls. We consider cases where (a) both walls preferentially attract the same component (A), and (b) one wall attracts A and the other wall attracts B (with the same strength). We focus on the interplay of phase separation and wetting at the walls, which is referred to as {\it surface-directed spinodal decomposition} (SDSD). The formation of SDSD waves at the two surfaces, with wave-vectors oriented perpendicular to them, often results in a metastable layered state (also referred to as ``stratified morphology''). This state is reminiscent of th…

SpinodalMaterials scienceMorphology (linguistics)Condensed matter physicsSpinodal decompositionKineticsFOS: Physical sciencesCondensed Matter - Soft Condensed MatterCondensed Matter::Soft Condensed MatterPhysics::Fluid DynamicsMetastabilityPerpendicularSoft Condensed Matter (cond-mat.soft)WettingThin filmPhysical review. E, Statistical, nonlinear, and soft matter physics
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Self-assembly of a bioelastomeric structure: solution dynamics and the spinodal and coacervation lines.

1990

The stability, metastability, and instability regions of aqueous solutions of a representative synthetic bioelastomeric polymer, poly (Val-Pro-Gly-Val-Gly), were determined by a combined use of elastic and quasi-elastic light scattering experiments. The approach followed here offers the attractive advantage of singling out the relevant contributions to the total scattering even in the presence of traces of noninteracting larger sized impurities. Conclusions so reached were checked by means of independent experiments. The present results provide descriptions of the very early events in the physics of bioelastogenesis in terms of general polymer science and phase transitions, and in terms of …

SpinodalPhase transitionChemical PhenomenaLightStereochemistryMolecular Sequence DataBiophysicsBiochemistryInstabilityLight scatteringBiomaterialsMolecular dynamicsMetastabilityScattering RadiationAmino Acid SequencePhase diagramQuantitative Biology::BiomoleculesScatteringChemistryChemistry PhysicalOrganic ChemistryTemperatureGeneral MedicineSolutionsChemical physicsPeptidesBiopolymers
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Protein aggregation/crystallization and minor structural changes: universal versus specific aspects.

2007

AbstractProtein association covers wide interests in biophysics, protein science, and biotechnologies, and it is often viewed as governed by conformation details. More recently, the existence of a universal physical principle governing aggregation/crystallization processes has been suggested by a series of experiments and shown to be linked to the universal scaling properties of concentration fluctuations occurring in the proximity of a phase transition (spinodal demixing in the specific case). Such properties have provided a quantitative basis for capturing kinetic association data on a universal master curve, ruled by the normalized distance of the state of the system from its instability…

SpinodalPhase transitionChemistryProtein ConformationCircular DichroismLasersBiophysicsNucleationSupramolecular AssembliesInstabilityUniversality (dynamical systems)law.inventionCrystallographyProtein structureModels ChemicallawChemical physicsAnimalsScattering RadiationMuramidaseCrystallizationCrystallizationScalingChickensBiophysical journal
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