Search results for "interfaces"

showing 10 items of 1258 documents

Affinity Distributions of a Molecularly Imprinted Polymer Calculated Numerically by the Expectation-Maximization Method

2003

Affinity distributions are calculated from adsorption isotherm data obtained for the enantiomers of L- and D-phenylalanine anilide (PA) on native and thermally annealed polymers molecularly imprinted with L-PA. The calculation is obtained with an iterative algorithm called expectation-maximization that does not require prior fit of the data to an isotherm model before inversion and thus yields a distribution indicative of the data only. The results show bimodal distributions, suggestive of a two-site model describing relatively selective and nonselective adsorption modes of the L-enantiomer and a corresponding unimodal/nonselective adsorption mode for the D-enantiomer. The nonselective adso…

chemistry.chemical_classificationMaterials scienceGaussianAnalytical chemistryMolecularly imprinted polymerSurfaces and InterfacesPolymerCondensed Matter Physicssymbols.namesakeAdsorptionDistribution (mathematics)chemistrySelective adsorptionExpectation–maximization algorithmElectrochemistrysymbolsGeneral Materials ScienceEnantiomerSpectroscopyLangmuir
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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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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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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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Magnetic molecular nanostructures: Design of magnetic molecular materials as monolayers, multilayers and thin films

2007

In this paper we summarize the importance and versatility of the molecular approach in the design and development of novel magnetic molecular materials. These materials processing, in order to obtain controlled molecular structures at the nanoscale, will also be remarked.

chemistry.chemical_classificationMaterials scienceNanostructureGeneral Physics and AstronomyNanotechnologySurfaces and InterfacesGeneral ChemistryCondensed Matter PhysicsSurfaces Coatings and FilmsCoordination complexNanolithographychemistryMonolayerMoleculeSelf-assemblyThin filmNanoscopic scaleApplied Surface Science
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Second harmonic generation in self-assembled alternating multilayers of hemicyanine containing polymers and polyvinylamine

1995

Abstract Assembly of noncentrosymmetric multilayers is a facile technique for preparing noncentrosymmetric films avoiding electrical poling procedures and problems from subsequent relaxation of the induced orientational order. A maximum Xzzz of 13 × 10−9 esu was achieved for the assembly of up to six layers. Current problems are the long-term hydrolysation of the hemicyanine nonlinear optical chromophores and the reduction of polar orientation with increasing layer thickness.

chemistry.chemical_classificationMaterials scienceNanostructurebusiness.industrySuperlatticePolingRelaxation (NMR)Metals and AlloysAnalytical chemistrySecond-harmonic generationSurfaces and InterfacesPolymerChromophoreSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryMaterials ChemistryOptoelectronicsPolarbusinessThin Solid Films
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Architecture, self-assembly and properties of well-defined hybrid polymers based on polyhedral oligomeric silsequioxane (POSS)

2013

Abstract Well-defined hybrid polymers based on polyhedral oligomeric silsequioxane (POSS) with a variety of architectures have been developed, including telechelic polymers, block copolymers and star-shaped polymers. The synthesis, self-assembly and properties of this kind of materials are reviewed. Well-defined POSS-containing hybrid polymers can be constructed by living polymerization techniques, such as ring-opening polymerization and living free-radical polymerization or the combination of living polymerization and coupling reactions, such as click chemistry and hydrosilylation. The self-assembly behavior of well-defined POSS-containing hybrid polymers is also described in detail. The P…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsHydrosilylationOrganic ChemistryNanotechnologySurfaces and InterfacesPolymerROMPchemistry.chemical_compoundchemistryPolymerizationPolymer chemistryMaterials ChemistryCeramics and CompositesCopolymerClick chemistryLiving polymerizationSelf-assemblyProgress in Polymer Science
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Linear–dendritic block copolymers: The state of the art and exciting perspectives

2011

Concurrent with the rapid development of both dendrimers and hyperbranched polymers, a novel class of block copolymer architectures has emerged from the combination of these dendritic architectures with linear chains, the “linear–dendritic block copolymers” (LDBCs). This review gives a comprehensive summary of the state of the art in this rapidly developing field from pioneering early work to promising recent approaches.The different strategies leading to these hybrid architectures with either perfect dendrimer/dendron building blocks or imperfect, yet more conveniently accessible hyperbranched segments, are reviewed and compared. The consequences of the unusual polymer topology for supramo…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryHyperbranched polymersSupramolecular chemistrySolid-stateNanotechnologySurfaces and InterfacesPolymerchemistryDendrimerPolymer chemistryMaterials ChemistryCeramics and CompositesCopolymerState (computer science)Topology (chemistry)Progress in Polymer Science
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Switching of Polymer Brushes

1999

Polymer coatings of brushlike monolayers composed of two different polymers, polystyrene and poly(2-vinylpyridine), are grafted by radical polymerization on the surface of silicon wafers. Thickness, grafting density, molecular weight of grafted chains, and the composition of the coatings were regulated by grafting time, monomer concentration, and additional initiator in solution. A typical dry film thickness is between 10 and 100 nm, and the molecular weights of the components range from 100 to 300 kg/mol. The fabricated coatings turn out to be sensitive to the composition of the environment. For instance after exposition to toluene the layer becomes hydrophobic and the top of the layer is …

chemistry.chemical_classificationMaterials scienceRadical polymerizationSurfaces and InterfacesPolymerCondensed Matter PhysicsContact anglechemistry.chemical_compoundMonomerChemical engineeringchemistryX-ray photoelectron spectroscopyMonolayerElectrochemistryGeneral Materials SciencePolystyreneLayer (electronics)SpectroscopyLangmuir
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