Search results for "Surfaces"

showing 10 items of 2837 documents

Covalently attached polymer mono- and multilayers on silanized glass substrates

1996

Abstract Applying grazing incidence FTIR and ellipsometry, the reaction of poly [(1-methyl-vinyl isocyanate)-alt-(maleic anhydride)](IAP) with amino-silanized glass and silicon oxide surfaces has been investigated. A reactive surface containing isocyanate and anhydride groups was formed after the adsorption of the polymer. The layer could be further functionalized using 2-aminoethanol. Multilayers could be built up by adsorbing a second layer of IAP onto an already reacted first layer of IAP.

chemistry.chemical_classificationMaterials scienceMetals and AlloysMaleic anhydrideSurfaces and InterfacesPolymerIsocyanateSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundAdsorptionchemistrySilanizationPolymer chemistryMaterials ChemistryFourier transform infrared spectroscopySilicon oxideLayer (electronics)Thin Solid Films
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Formation of nanorods by self-assembly of alkyl-substituted polyphenylene dendrimers on graphite

2000

Alkyl-substituted polyphenylene dendrimers with a tetrahedral or disk-like shape form self-assembled monolayers on graphite (HOPG) which show complex supramolecular structures, such as parallel rods of 6 nm diameter or two-dimensional crystals.

chemistry.chemical_classificationMaterials scienceMetals and AlloysSupramolecular chemistryNanotechnologyGeneral ChemistryCatalysisRodSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographychemistryDendrimerMonolayerMaterials ChemistryCeramics and CompositesNanorodGraphiteSelf-assemblyAlkylChemical Communications
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Structured Nanoparticles from the Self-Assembly of Polymer Blends through Rapid Solvent Exchange

2017

Molecular dynamics simulations were performed to study systematically the rapid mixing of a polymer blend in solution with a miscible nonsolvent. In agreement with experiments, we observe that polymers self-assemble into complex nanoparticles, such as Janus and core-shell particles, when the good solvent is displaced by the poor solvent. The emerging structures can be predicted on the basis of the surface tensions between the polymers as well as between the polymers and the surrounding liquid. Furthermore, the size of the nanoparticles can be independently tuned through the mixing rate and the polymer concentration in the feed stream; meanwhile, the composition of the nanoparticles can be c…

chemistry.chemical_classificationMaterials scienceMixing (process engineering)Nanoparticle02 engineering and technologySurfaces and InterfacesPolymer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesSolventMolecular dynamicsChemical engineeringchemistryPolymer chemistryElectrochemistryGeneral Materials ScienceParticle sizePolymer blendJanus0210 nano-technologySpectroscopyLangmuir
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On the Stability of Polymeric Nanoparticles Fabricated through Rapid Solvent Mixing.

2018

We study the stability of polymeric nanoparticles fabricated through the rapid mixing of polymers in a good solvent with a poor solvent that is miscible with the good solvent. In previous experiments where water was used as the poor solvent, a negative surface charge was measured on the precipitated nanoparticles, which led to the long-time stability of the dispersion. It was argued that these charges originate presumably from either water or hydroxide adsorption at the hydrophobic nanoparticle surface or from impurities in the feed streams that preferentially adsorb on the precipitated nanoparticles. To elucidate the origin of this stabilization mechanism, we performed experiments wherein …

chemistry.chemical_classificationMaterials scienceMixing (process engineering)Nanoparticle02 engineering and technologySurfaces and InterfacesPolymer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesSolventchemistry.chemical_compoundAdsorptionChemical engineeringchemistryElectrochemistryHydroxideGeneral Materials ScienceSurface charge0210 nano-technologyDispersion (chemistry)SpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Effect of the Components Molar Mass and of the Mixing Conditions on the Compatibilization of PE/LCP Blends by PE-g-LCP Copolymers

1999

The rheology, morphology, and mechanical properties of blends of high-density polyethylene (HDPE) with a semiflexible liquid crystalline copolyester (SBH) were studied in order to assess the compatibilizing ability of added PE-g-SBH copolymers, and its dependence on the molar mass of the PE matrix, and on the technique used for blend preparation. The PE-g-SBH copolymers were synthesized as described in previous articles, either by the polycondensation of the SBH monomers in the presence of a functionalized PE sample containing free carboxyl groups, or by reactive blending of the latter polymer with preformed SBH. Two samples of HDPE having different molar masses, and two samples of SBH with…

chemistry.chemical_classificationMaterials scienceMolar massCondensation polymerPolymers and PlasticscompatibilizationGeneral ChemistryPolymerCompatibilizationPolyethyleneCopolyesterSurfaces Coatings and Filmschemistry.chemical_compoundchemistrypolyethylene-LCP blendmorphologyMaterials ChemistryCopolymerrheologyHigh-density polyethyleneComposite material
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Interfacial Tensions from Drop Retraction versus Pendant Drop Data and Polydispersity Effects

2004

Interfacial tensions sigma were measured by means of both methods for the following polymer pair: polyisobutylene (PIB 3) plus poly(dimethylsiloxane) (PDMS 152) and poly(dimethyl-co-methylphenylsiloxane) (CoP26*) plus PDMS 48. The numbers after the abbreviation state the molar masses in kilograms; the homopolymers exhibit polydispersities on the order of 2. The reliability of the method of drop retraction is backed up by systematic measurements, which demonstrate that it is possible to study the time evolution of sigma. Because of the free choice of the phases (drop or matrix) and the possibility to vary the overall composition of the system in a wide range, drop retraction yields more info…

chemistry.chemical_classificationMaterials scienceMolar massDrop (liquid)DispersityTime evolutionThermodynamicsSurfaces and InterfacesPolymerCondensed Matter PhysicsDrop methodSurface tensionchemistryPolymer chemistryElectrochemistryGeneral Materials ScienceSpectroscopyLangmuir
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Polyisoprene-carbon black nanocomposites as tensile strain and pressure sensor materials

2004

Abstract Electrically conductive polymer composites (ECPC) are shown as prospective large-size flexible pressure and stretch sensors for detecting of dangerous deformations and vibrations of vehicle parts. Reversible change of resistance dependent on stretch and pressure is obtained in electro-conductive polymer nanocomposites. At certain concentrations of carbon nano-particles a change of electrical resistance by more than four orders is observed at 40% relative stretch. The maximum sensitivity of nanocomposites is observed in the vicinity of the transition of electro-conductive percolation. Nanocomposites exhibit a very weak semiconductor-like temperature dependence of resistance. The ten…

chemistry.chemical_classificationMaterials scienceNanocompositePolymer nanocompositeMetals and AlloysPolymerCarbon blackCondensed Matter PhysicsMicrostructureSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsStress (mechanics)chemistryElectrical resistance and conductancePercolationElectrical and Electronic EngineeringComposite materialInstrumentationSensors and Actuators A: Physical
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Towards completely miscible PMMA nanocomposites reinforced by shear-stiff, nano-mica

2014

Abstract Optimizing the reinforcement of polymers with nanoplatelets requires optimization of the aspect ratio and the moduli of the filler while providing a complete stress transfer. Employing a novel shear-stiff, nano-mica with large aspect ratio, we focus on maximizing the interfacial interaction between filler and matrix. External surfaces of the nano-mica were selectively modified by a polycationic macro-initiator and two PMMA-polymer brushes of length below and above critical entanglement length, respectively, and the mechanical properties of the three PMMA nanocomposites were measured. The multiple electrostatic anchoring groups of the macro-initiator not only provide reliable adhesi…

chemistry.chemical_classificationMaterials scienceNanocompositePolymerengineering.materialSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialsColloid and Surface ChemistrychemistryCoatingPolymerizationLiquid crystalTransmission electron microscopyNano-Polymer chemistryengineeringMicaComposite materialJournal of Colloid and Interface Science
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Modeling and stress-strain characteristics of the mechanical properties of carbon-nanotube-reinforced poly(vinyl acetate) nanocomposites

2011

Polymer/carbon nanotube (CNT) composites are one of the most perspective advanced materials developed in recent years. The properties of CNT-reinforced polymer composites, however, strongly depend on structural aspects of the nanostructured filler and on its dispersion quality in a polymer matrix. Consequently, this research was devoted to the investigation of multiwalled-CNT-modified poly(vinyl acetate) (PVAc) composites with respect to the mechanical property dependence on some structural characteristics of CNTs. PVAc/CNT nanocomposites were obtained with a solution casting technique. The amount of CNTs was changed from 0.01 up to 2 wt %. The stress–strain characteristics of PVAc/CNT nano…

chemistry.chemical_classificationMaterials scienceNanocompositePolymers and PlasticsPolymer nanocompositeStress–strain curveGeneral ChemistryCarbon nanotubePolymerSurfaces Coatings and Filmslaw.inventionchemistry.chemical_compoundchemistrylawUltimate tensile strengthMaterials ChemistryVinyl acetateComposite materialElastic modulusJournal of Applied Polymer Science
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Luminescent and Magnetoresponsive Multifunctional Chalcogenide/Polymer Hybrid Nanoparticles

2013

Cadmium sulfide/magnetite/polymer multifunctional hybrid nanoparticles are prepared by crystallizing CdS in a controlled manner on the surface of phosphonate-functionalized polystyrene particles with a magnetic core. The supporting polymer magnetoresponsive nanoparticles are produced by a modified miniemulsion polymerization process: a first miniemulsion containing the core monomer (styrene) and a phosphonate-functionalized surface-active monomer is mixed with a second miniemulsion containing magnetite nanoparticles capped with oleic acid and the same surface-active monomer. The chalcogenide formation occurs in situ at the surface of the polymer particles by adding a precipitating agent (so…

chemistry.chemical_classificationMaterials scienceNanoparticlePolymerSodium sulfideCadmium sulfideSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMiniemulsionchemistry.chemical_compoundGeneral EnergyMonomerchemistryPolymerizationPolymer chemistryPolystyrenePhysical and Theoretical ChemistryThe Journal of Physical Chemistry C
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