Search results for "surfaces"

showing 10 items of 2837 documents

Glassy dynamics of simulated polymer melts: Coherent scattering and van Hove correlation functions

2001

Whereas the first part of this paper dealt with the relaxation in the β-regime, this part investigates the final relaxation (α-relaxation) of a simulated polymer melt consisting of short non-entangled chains in the supercooled state above the critical temperature of ideal mode-coupling theory (MCT). The temperature range covers the onset of a two-step relaxation behaviour down to a temperature merely 2% above . We monitor the incoherent intermediate scattering function as well as the coherent intermediate scattering function of both a single chain and the melt over a wide range of wave numbers q. Upon approaching the coherent α-relaxation time of the melt increases strongly close to the max…

chemistry.chemical_classificationMax QPhysicsMaterials scienceCondensed matter physicsScatteringDynamics (mechanics)Relaxation (NMR)BiophysicsAlpha (ethology)PolymerSurfaces and InterfacesGeneral ChemistryAtmospheric temperature rangePower lawchemistryRadius of gyrationExponentRelaxation (physics)General Materials ScienceSoft matterStructure factorBiotechnologyThe European Physical Journal E
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2021

Water-in-salt systems, i.e., super-concentrated aqueous electrolytes, such as lithium bis(trifluoromethanesulfonyl)imide (21 mol/kgwater), have been recently discovered to exhibit unexpectedly large electrochemical windows and high lithium transference numbers, thus paving the way to safe and sustainable charge storage devices. The peculiar transport features in these electrolytes are influenced by their intrinsically nanoseparated morphology, stemming from the anion hydrophobic nature and manifesting as nanosegregation between anions and water domains. The underlying mechanism behind this structure-dynamics correlation is, however, still a matter of strong debate. Here, we enhance the apol…

chemistry.chemical_classificationMesoscopic physicsDiffusionchemistry.chemical_elementSalt (chemistry)ElectrolyteElectrochemistrySurfaces Coatings and FilmsIonchemistry.chemical_compoundchemistryChemical physicsMaterials ChemistryLithiumPhysical and Theoretical ChemistryImideThe Journal of Physical Chemistry B
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P-chirogenic organocatalysts: application to the aza-Morita–Baylis–Hillman (aza-MBH) reaction of ketimines

2013

The P-chirogenic organocatalysts were found to promote the enantioselective aza-Morita-Baylis-Hillman reaction of ketimines derived from acyclic α-keto esters. In the P-chirogenic organocatalyzed aza-MBH reactions, α,α-disubstituted α-amino acid derivatives were obtained in high yields with high enantioselectivities (up to 97% ee).

chemistry.chemical_classificationMetals and AlloysEnantioselective synthesisStereoisomerismStereoisomerismGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysisAmino acidchemistryNitrilesMaterials ChemistryCeramics and CompositesOrganic chemistryIminesAmino AcidsChemical Communications
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Oxamato-based coordination polymers: recent advances in multifunctional magnetic materials

2014

The design and synthesis of novel examples of multifunctional magnetic materials based on the so-called coordination polymers (CPs) have become very attractive for chemists and physicists due to their potential applications in nanoscience and nanotechnology. However, their preparation is still an experimental challenge, which requires a deep knowledge of coordination chemistry and large skills in organic chemistry. The recent advances in this field using a molecular-programmed approach based on rational self-assembly methods which fully exploit the versatility of the coordination chemistry of the barely explored and evergreen family of N-substituted aromatic oligo(oxamato) ligands are prese…

chemistry.chemical_classificationMetals and AlloysNanotechnologyGeneral ChemistryPolymerCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCoordination complexchemistryMaterials ChemistryCeramics and CompositesDeep knowledgeExperimental challengeChem. Commun.
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1,3-Dimethylimidazolium-2-carboxylate: the unexpected synthesis of an ionic liquid precursor and carbene-CO2 adductElectronic supplementary informati…

2002

1,3-Dimethylimidazolium-2-carboxylate is formed in good yield, rather than the anticipated organic salt, 1,3-dimethylimidazolium methyl carbonate, as the reaction product resulting from both N-alkylation and C-carboxylation of 1-methylimidazole with dimethyl carbonate; the crystal structure of the zwitterion exhibits π-stacked rings and two-dimensional sheets constructed by hydrogen-bonds from imidazolium-ring hydrogens to the carboxylate group.

chemistry.chemical_classificationMetals and AlloysSalt (chemistry)General ChemistryCrystal structureCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAdductchemistry.chemical_compoundchemistryZwitterionPolymer chemistryIonic liquidMaterials ChemistryCeramics and CompositesOrganic chemistryCarboxylateDimethyl carbonateCarbeneChemical Communications
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Physicochemical Properties of Copper(II) Bis(2-ethylhexyl) Sulfosuccinate Reversed Micelles

1998

Abstract Measurements of some physicochemical properties (density, viscosity, conductance, UV–vis spectra, IR spectra) of the water/copper(II) bis(2-ethylhexyl) sulfosuccinate (Cu(DEHSS) 2 )/CCl 4 microemulsions, at a fixed surfactant molal concentration ([Cu (DEHSS) 2 ] = 0.05003 mol kg −1 ), as function of the molar ratio R ( R = [water]/[DEHSS − ]) have been performed at 25°C. Information on some structural and dynamical properties of the water-containing Cu(DEHSS) 2 reversed micelles and of their evolution with R are derived from the experimental results. The comparison with the same properties of water-containing sodium bis(2-ethylhexyl) sulfosuccinate reversed micelles allows to evide…

chemistry.chemical_classificationMolalityAnalytical chemistrychemistry.chemical_elementConductanceInfrared spectroscopyCopperMicelleSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialsColloid and Surface ChemistrychemistryPulmonary surfactantPhysical chemistryMicroemulsionCounterionJournal of Colloid and Interface Science
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Morphology and Rheology of HDPE/LCP Blends Compatibilized by a Novel PE-g-LCP Copolymer

1999

A novel graft copolymer (PE-g-LCP) consisting of polyethylene (PE) backbones and liquid crystalline polymer (LCP) branches was synthesized via reactive blending of an acrylic acid-functionalized PE (Escor 5000 by Exxon) with a semiflexible LCP (SBH 1 : 1 : 2 by Eniricerche S.p.A.). The crude reactive blending product (COP) was shown by investigation of the fractions soluble in boiling toluene and xylene and of the residue to contain unreacted Escor and SBH, together with the graft copolymer forming the interphase. The compatibilizing activity of COP for PE/SBH blends, compared to that of pure Escor, was investigated using two PE grades. The COP addition into 80/20 PE/SBH blends caused a muc…

chemistry.chemical_classificationMolar massMaterials sciencePolymers and PlasticsGeneral ChemistryCompatibilizationPolymerPolyethyleneSurfaces Coatings and Filmschemistry.chemical_compoundRheologychemistryChemical engineeringPolymer chemistryMaterials ChemistryCopolymerHigh-density polyethylenePolymer blend
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Loading of polymer nanocarriers: Factors, mechanisms and applications

2014

Abstract The progress in synthetic polymer chemistry has allowed the precise design of hybrid and multifunctional colloidal particles, which differ in type, size and shape, thus enhancing their possible applications as target-oriented carriers of low and high molar mass active species. This survey discusses the basic principles and factors, associated with the process of loading of polymeric nanoparticles. For the purpose of this review, the polymeric nano-carriers are divided into five most studied types: micelles, nanogels, capsules (incl. vesicles), dendrimers, and hybrid nanoparticles with porous cores. Factors influencing the loading are described and their importance discussed. An imp…

chemistry.chemical_classificationMolar massMaterials sciencePolymers and PlasticsVesicleOrganic ChemistryNanoparticleNanotechnologySurfaces and InterfacesPolymerPolymeric nanoparticlesMicellechemistryDendrimerMaterials ChemistryCeramics and CompositesNanocarriersProgress in Polymer Science
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Viscosity-molecular weight relationship for cellulose solutions in either NMMO monohydrate or cuen

2010

The intrinsic viscosities, [η], of nine cellulose samples, with molar masses from 50 × 103 to 1 390 × 103 were determined in the solvents NMMO*H2O (N-methyl morpholin N-oxide hydrate) at 80°C and in cuen (copper II-ethlenediamine) at 25°C. The evaluation of these results with respect to the Kuhn–Mark–Houwink relations shows that the data for NMMO*H2O fall on the usual straight line in the double logarithmic plots only for M ≤ 158 103; the corresponding [η]/M relation reads log ([η]/mL g−1) = –1.465 + 0.735 log M. Beyond that molar mass [η] remains almost constant up to M ≈ 106 and increases again thereafter. In contrast to NMMO*H2O the cellulose solutions in cuen behave normal and the Kuhn–…

chemistry.chemical_classificationMolar massPolymers and PlasticsIntrinsic viscosityAnalytical chemistrychemistry.chemical_elementGeneral ChemistryPolymerCopperSurfaces Coatings and Filmschemistry.chemical_compoundViscositychemistryPolymer chemistryMaterials ChemistryCelluloseta216Hydrateta215Journal of Applied Polymer Science
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Polymeric gegenions induced variability and mobility of amphiphilic supramolecular structures on solid substrates

1992

Abstract The micromorphological variations of amphiphilic L -glutamate derivatives at air-substrate interfaces due to an adjacent mobile polymer matrix have been investigated via fluorescence microscopy. Adjusted monolayers of the L -glutamate derivatives have been transferred by LB technique out of different aggregation states onto various substrates. The substrates have been prepared by successive polymer preadsorption to the solid support. The influence of the adjacent polymer layers on the domain morphology as a function of water content and temperature has been examined intensively. Moreover, reversible domain changes induced by temperature variation of the transferred films have been …

chemistry.chemical_classificationMorphology (linguistics)Metals and AlloysAnalytical chemistryFluorescence spectrometrySupramolecular chemistrySurfaces and InterfacesPolymerSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMatrix (chemical analysis)chemistryChemical engineeringAmphiphileMonolayerMaterials ChemistryFluorescence microscopeThin Solid Films
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