Search results for "Polymer adsorption"

showing 10 items of 12 documents

Aqueous phase/nanoparticles interface: hydroxypropyl cellulose adsorption and desorption triggered by temperature and inorganic salts

2012

The study highlighted the main forces driving the adsorption of hydroxypropyl cellulose (HPC) onto clay nanoparticles with a disk-like shape (Laponite RD). Modeling the isothermal titration calorimetry data provided the key thermodynamic properties, which enabled us to discuss the microscopic aspects contributing to the energetic and the entropic changes of the polymer adsorption at the nanoparticle/liquid interface. We evidenced that the process is strongly enthalpy-driven and that the interactions lead to constraints of the HPC configuration at interface. The functionalized nanoparticles enhanced the polymer solubility in water expanding the one-phase area of the binodal curve. Temperatur…

BinodalMaterials scienceHydroxypropyl cellulosenanoparticles interface cellulose calorimetryNanoparticleIsothermal titration calorimetryGeneral ChemistryPolymer adsorptionCondensed Matter Physicschemistry.chemical_compoundAdsorptionchemistryChemical engineeringDesorptionOrganic chemistrySolubilitySettore CHIM/02 - Chimica Fisica
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Biopolymer-Targeted Adsorption onto Halloysite Nanotubes in Aqueous Media.

2017

Studies on the adsorption of biopolymers onto halloysite nanotubes (HNTs) in water were conducted. Three polymers with different charges-anionic (pectin), neutral (hydroxypropyl cellulose), and cationic (chitosan)-were chosen. The thermodynamic parameters for the adsorption of polymers onto the HNT surface were determined by isothermal titration calorimetry (ITC). The experimental data were interpreted based on a Langmuir adsorption model. The standard variations in free energy, enthalpy, and entropy of the process were obtained and discussed. Turbidimetry was used to evaluate the stability of functionalized nanoparticles in water. The ζ-potential clarified the surface charge properties of …

Materials scienceBiopolymerFunctionalized nanotube02 engineering and technologyengineering.materialHydroxypropyl cellulose010402 general chemistry01 natural sciencesHalloysitechemistry.chemical_compoundsymbols.namesakeAdsorptionEnthalpyKaoliniteLangmuir adsorption modelPolymer chemistryElectrochemistryHalloysite nanotube (HNTs)General Materials ScienceSurface chargeFree energyPolymerSpectroscopyYarn Functionalized nanoparticleHydroxypropyl celluloseLangmuir adsorption modelWaterIsothermal titration calorimetrySurfaces and InterfacesPolymer adsorptionThermal Propertie021001 nanoscience & nanotechnologyCondensed Matter PhysicsPectin0104 chemical sciencesBiomoleculeNanotubechemistryChemical engineeringengineeringsymbolsIsothermal titration calorimetryBiopolymerAdsorption0210 nano-technologySurface charge propertieThermodynamic parameter Polymers ChitosanLangmuir : the ACS journal of surfaces and colloids
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Semiflexible polymers confined in a slit pore with attractive walls: two-dimensional liquid crystalline order versus capillary nematization

2017

Semiflexible polymers under good solvent conditions interacting with attractive planar surfaces are investigated by Molecular Dynamics (MD) simulations and classical Density Functional Theory (DFT). A bead-spring type potential complemented by a bending potential is used, allowing variation of chain stiffness from completely flexible coils to rod-like polymers whose persistence length by far exceeds their contour length. Solvent is only implicitly included, monomer-monomer interactions being purely repulsive, while two types of attractive wall-monomer interactions are considered: (i) a strongly attractive Mie-type potential, appropriate for a strictly structureless wall, and (ii) a corrugat…

Persistence lengthCanonical ensembleQuantitative Biology::BiomoleculesCondensed matter physicsCapillary actionChemistry02 engineering and technologyGeneral ChemistryPolymer adsorption021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesCondensed Matter::Soft Condensed MatterMolecular dynamicsLiquid crystalChemical physicsPhase (matter)0103 physical sciencesDensity functional theory010306 general physics0210 nano-technologySoft Matter
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Polymer solutions confined in slit-like pores with attractive walls: An off-lattice Monte Carlo study of static properties and chain dynamics

1996

Using a bead spring model of flexible polymer chains, the density profiles and chain configurational properties of polymer solutions confined between parallel plates were studied. A wide range of density ϕ, chain length N, and strength e of a short-range attractive wall potential was investigated. Both a temperature T in the good solvent regime (T > θ, θ being the Theta temperature where a chain in unconfined bulk three-dimensional solution would behave ideally) and a temperature in the bad solvent regime (T θ) show a crossover from two-dimensional excluded volume behavior (Rg ∝ N2ν with ν = 3/4) to ideal random walk behavior (ν = 1/2), the relaxation times show effective exponents Zeff (τ …

chemistry.chemical_classificationCondensed matter physicsChemistryDiffusionMonte Carlo methodTheta solventPolymerPolymer adsorptionRandom walkComputer Science ApplicationsCondensed Matter::Soft Condensed MatterComputational Theory and MathematicsExcluded volumeRelaxation (physics)General Materials ScienceJournal of Computer-Aided Materials Design
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Critical adsorption of a single macromolecule in polymer brushes.

2014

The adsorption of long flexible macromolecules by polymer brush-coated surfaces is studied by molecular dynamics simulations and by calculations using density functional and self-consistent field theories. The case of repulsive interactions between the substrate surface and the monomers of both the brush polymers and the extra chains that can get absorbed into the brush is considered. Under good solvent conditions, critical absorption can occur, if the interaction between the monomers of the brush polymers and the extra chain is (weakly) attractive. It is shown that it is possible to map out the details of the critical absorption transition, if the chain length and/or the grafting density o…

chemistry.chemical_classificationMaterials scienceGeneral ChemistryPolymerPolymer adsorptionCondensed Matter Physicschemistry.chemical_compoundMolecular dynamicsMonomerAdsorptionchemistryChemical physicsPolymer chemistryFinite potential wellAbsorption (chemistry)MacromoleculeSoft matter
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Polyethylene glycol/clay nanotubes composites

2012

Nanocomposites of poly(ethylene) glycol (PEG) 20000 filled with clay nanotubes (HNTs) were prepared. The thermal properties obtained from thermogravimetry and differential scanning calorimetry were correlated to the morphology imaged by scanning electron microscopy. Low amounts of HNTs generate compact structure while large amounts of HNTs create craters and voids. The decrease of polymer degradation temperature in the presence of large amount of nanoclay (ca. 80 wt%) is a consequence of the morphology at the mesoscale range. The thermal opposite effect observed in the HNTs low regime (up to ca. 20 wt%) is due to the gas entrapment into the nanoparticles lumen. The quantitative analysis of …

chemistry.chemical_classificationMaterials scienceNanocompositeNanoparticlePolymerPolymer adsorptionPolyethylene glycolCondensed Matter PhysicsNanotube polymerThermogravimetrychemistry.chemical_compoundDifferential scanning calorimetryPolymer degradationchemistryPhysical and Theoretical ChemistryComposite materialSettore CHIM/02 - Chimica FisicaJournal of Thermal Analysis and Calorimetry
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Mechanical Properties of Single Molecules and Polymer Aggregates

2013

This chapter deals with the mechanical properties of single polymer chains, aggregates, and supramolecular complexes. The topics discussed cover a broad range from fundamental statistical mechanics of the equilibrium elastic properties of single polymer chains to details of the behavior of binding pockets in biomolecular assemblies as observed by force spectroscopy. The first section treats the equilibrium mechanical properties of single polymer chains in various environments, investigated via extensive simulations employing coarse-grained models that have proven extremely successful in many branches of polymer physics, namely the bond-fluctuation model and the self-avoiding walk model. Apa…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceCatenaneForce spectroscopySupramolecular chemistryNanotechnologyPolymer adsorptionStatistical mechanicsPolymerMolecular dynamicschemistryChemical physicsPolymer physics
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Polymer absorption in dense polymer brushes vs. polymer adsorption on the brush-solvent interface

2014

Molecular-dynamics simulations of a coarse-grained model of a dense brush of flexible polymers (of type A) interacting with a long flexible macromolecule (of type B) are presented, considering the case of an attractive AB interaction, while effective interactions between AA and BB pairs of monomers are repulsive. Varying the strength of the attraction between unlike monomers, an adsorption transition at some critical value is found, where the B-chain is bound to the brush-solvent interface, similar to the adsorption on a planar solid substrate. However, when is much higher than , the long macromolecule is gradually “sucked in” the brush, developing many pieces that are locally stretched in …

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceRelaxation (NMR)General Physics and AstronomyPolymerPolymer adsorptionCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundReptationMonomerAdsorptionchemistryChemical physicsAbsorption (chemistry)MacromoleculeEPL (Europhysics Letters)
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Pattern-recognising Polymer Adsorption on Structured Surfaces: Gaussian Polymers vs. Freely Jointed Chains

2014

Abstract Selective adsorption of homopolymers is exploited as a model for pattern recognition. To this end the strong adsorption regime of Gaussian polymers adsorbed on a regularly structured surface is investigated for square and triangular lattices within a discrete Edwards model. The equilibrium behaviour of the specific heat, the gyration tensor and the (nematic) bond order tensor are analysed and compared to the properties for adsorbed freely jointed polymer chains.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials sciencepattern recognitionGyration tensorPolymerPolymer adsorptionPhysics and Astronomy(all)Bond orderMonte Carlo simulationsCondensed Matter::Soft Condensed MatterPolymer adsorptionCondensed Matter::Materials ScienceAdsorptionchemistryLiquid crystalChemical physicsSelective adsorptionTensorPhysics::Chemical PhysicsPhysics Procedia
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Semidilute and Concentrated Polymer Solutions near Attractive Walls:  Dynamic Monte Carlo Simulation of Density and Pressure Profiles of a Coarse-Gra…

1997

Using a bead−spring model of flexible polymer chains, we study polymer adsorption from solutions onto attractive planar walls, varying both the strength of the adsorption potential e and the concentration of the solution over a wide range. Treating the case of good solvents, the profiles of density and pressure are computed and it is shown that thermal equilibrium between the adsorbed layer and the bulk solution is obtained. The case of a wall with purely repulsive potential under otherwise identical conditions is treated for comparison. It is shown that for the strongly adsorbing wall there is a pronounced layering, while a layered structure at the repulsive wall occurs only for high conce…

chemistry.chemical_classificationThermal equilibriumPolymers and PlasticsChemistryOrganic ChemistryMonte Carlo methodPolymerPolymer adsorptionSurface energyCondensed Matter::Soft Condensed MatterInorganic ChemistryAdsorptionChemical physicsMaterials ChemistryStatistical physicsTotal pressureLayeringMacromolecules
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