Search results for "blend"

showing 10 items of 421 documents

Beyond the screen

2021

Our didactic experiences in the field of architectural design, in courses that have always had a strong workshop character, have been varied in recent years and have been carried out in different variants that, when considered as a whole, allow us to reflect on the problems and the challenges faced during the pandemic. Indeed, a didactic normally conducted with compulsory attendance suffered in a sudden and unexpected way from the cancellation of physical presence, the loss of contact with people and the “corporeality” of the project. Moreover, the absence of the physical space of the classroom (a scene inherent to the laboratory) soon led to the search for new tools and appropriate methods…

blended flexible trainingarchéacovid teaching research project methodArchitectureSettore ICAR/14 - Composizione Architettonica E Urbanabest practicesNA1-9428Festival dell'Architettura Magazine
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Janus Nanostructures from ABC/B Triblock Terpolymer Blends

2019

Lamella-forming ABC triblock terpolymers are convenient building blocks for the synthesis of soft Janus nanoparticles (JNPs) by crosslinking the B domain that is &ldquo

bulk morphologiestechnology industry and agricultureChemiemacromolecular substancesArticlelcsh:QD241-441block copolymersForschungszentren » Center for Nanointegration Duisburg-Essen (CENIDE)lcsh:Organic chemistryddc:540DPD simulationspolymer blendingddc:541Janus nanostructuresFakultät für Chemie » Physikalische ChemiePolymers
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Joint Aqueous Solutions of Dextran and Bovine Serum Albumin: Coexistence of Three Liquid Phases

2014

The phase diagram of the system water/dextran (DEX)/BSA was measured as well as modeled. On the experimental side, cloud points were determined and the coexisting phases were analyzed. The theoretical calculations use an approach capable of describing solutions of chain polymers and of globular proteins with the same formalism. The required thermodynamic input comes from experiments concerning the binary subsystems, except for the polymer blend for which one interaction parameter had to be adjusted. Both sources of information yield the same essential features: the existence of a large composition area of immiscibility, starting from the subsystem DEX/BSA and extending well into the region …

chemistry.chemical_classificationAqueous solutionbiologyPolymersGlobular proteinAnalytical chemistryDextransSerum Albumin BovineSurfaces and InterfacesPolymerFlory–Huggins solution theoryCondensed Matter PhysicsSolutionschemistry.chemical_compoundDextranchemistryElectrochemistrybiology.proteinAnimalsCattleGeneral Materials SciencePolymer blendBovine serum albuminSpectroscopyPhase diagramLangmuir
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Phase Transitions of Polymer Blends and Block Copolymer Melts in Thin Films

1999

chemistry.chemical_classificationBinodalMolten statePhase transitionChromatographyMaterials sciencechemistryChemical engineeringCopolymerPolymerPolymer blendThin filmPhase diagram
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Treatment of poly(styrene-co-methacrylic acid)/poly(4-vinylpyridine) blends in solution under liquid–liquid phase-separation conditions. A new method…

2006

Phase diagrams are contributed for polymer mixture systems in solution. One polymer has proton-acceptor character and the other has growing proton-donor nature, which is reflected in the phase diagrams. Usually, these diagrams are obtained from size-exclusion chromatographic (SEC) measurements. A totally novel application, which is exposed in this report, is the construction of the phase diagram from the viscometric experiments of polymer mixtures. The evaluated binodal or cloud-point isotherms so built agree well with those from SEC. The results indicate an augmentation in the dimensions of donor polymer B, in the presence of acceptor polymer C, intensifying with the concentration of C, wh…

chemistry.chemical_classificationBinodalPolymers and PlasticsAnalytical chemistryGeneral ChemistryPolymerMiscibilitySurfaces Coatings and FilmsStyrenechemistry.chemical_compoundMethacrylic acidchemistryPolymer chemistryMaterials ChemistryCopolymerPolymer blendPhase diagramJournal of Applied Polymer Science
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‘Intrinsic’ profiles and capillary waves at interfaces between coexisting phases in polymer blends

2001

Abstract Lateral fluctuations in the local position of the center of the interface between coexisting phases in unmixed polymer blends lead to a broadening of interfacial widths; comparing self-consistent field predictions for the ‘intrinsic’ profile to simulations (or experiments), this ‘capillary wave’ broadening needs consideration. This problem has been studied by extensive Monte Carlo simulations of the bond fluctuation model for symmetrical polymer mixtures, both for free interfaces (between bulk phases) and for confined interfaces (in thin films between parallel walls). While the capillary wave predictions at large length scales are confirmed, the extraction of the ‘intrinsic’ profil…

chemistry.chemical_classificationCapillary waveMaterials scienceField (physics)Monte Carlo methodAnalytical chemistrySurfaces and InterfacesPolymerCondensed Matter::Soft Condensed MatterColloid and Surface ChemistrychemistryPosition (vector)Chemical physicsPolymer blendPhysical and Theoretical ChemistryThin filmBond fluctuation modelAdvances in Colloid and Interface Science
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Interfaces between coexisting phases of polymer mixtures: Comparison between Monte Carlo simulations and theoretical predictions

1997

Large scale Monte Carlo investigations of the interface between A-rich and B-rich phases of symmetric binary (AB) polymer mixtures are presented, using the bond fluctuation model of flexible chains with NA=NB=N=32 effective monomers. The temperature range studied, 0.144<T/Tc0.759, includes both the strong and the weak segregation limit. Interfacial free energy and interfacial structure are studied, and compared to predictions based on the selfconsistent field theory. Also the broadening of the interfacial width due to capillary waves is considered, and finite size effects due to the confinement of interfaces in thin films of polymer blends are discussed.

chemistry.chemical_classificationCapillary waveMaterials sciencePolymers and PlasticsOrganic ChemistryMonte Carlo methodThermodynamicsPolymerAtmospheric temperature rangeCondensed Matter PhysicsCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundMonomerchemistryMaterials ChemistryField theory (psychology)Statistical physicsPolymer blendThin filmMacromolecular Symposia
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Interfacial tension between polymer-containing liquids - Predictability and influences of additives

1999

The first part of the contribution deals with the interfacial tension, σ, of phase-separated polymer solutions in single or mixed solvents and of binary polymer blends as a function of the relative distance to the critical temperature of the system, special attention being paid to the possibilities of theoretical prediction. Two methods are discussed in more detail. One is based on a realistic description of the Gibbs energy of mixing as a function of composition, the second correlates σ with the length of the measured tie line. The second part is devoted to another aspect, namely the effects of additives on the interfacial tension between the coexisting phases of demixed polymer solutions …

chemistry.chemical_classificationChromatographyPolymers and PlasticsOrganic ChemistryMixing (process engineering)ThermodynamicsPolymerCondensed Matter PhysicsGibbs free energySurface tensionchemistry.chemical_compoundsymbols.namesakeMonomerchemistryMaterials ChemistryCopolymersymbolsPolymer blendTie lineMacromolecular Symposia
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The effect of pressure on the liquid–liquid phase equilibrium of two polydisperse polyalkylsiloxane blends

2002

The effect of pressure-induced immiscibility in polymer blends is investigated by experimental and theoretical methods. Experimental data of cloud point curves and critical points are obtained by turbidity measurements. The chosen system is a mixture of polydimethylsiloxane and polyhexylmethylsiloxane which is one of the very few polymer blends exhibiting pressure-induced immiscibility. This unusual behaviour is related to a critical temperature minimum of the critical curve and cloud point isopleths at positive pressure in the temperature–pressure diagram. The effect of the chain length on the critical temperature minimum is investigated here based on theoretical models. The effect of diff…

chemistry.chemical_classificationCloud pointMaterials sciencePolydimethylsiloxaneGeneral Physics and AstronomyThermodynamicsPolymerLower critical solution temperatureMiscibilityCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundchemistryCritical point (thermodynamics)Polymer blendPhysical and Theoretical ChemistryPhase diagramPhysical Chemistry Chemical Physics
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PHEA‐PLLA: A New Polymer Blend For Tissue Engineering Applications

2011

One of most important features that a material should have in order to be utilized for tissue engineering applications is its biocompatibility and its chemical surface. These properties are required for a high degree of cell adhesion on the scaffold. Poly‐L‐lactid acid (PLLA) is a biocompatible synthetic polymer approved by the Food and Drug Administration for human clinical applications. It has been largely employed, in the last years, as a constituent of surgical and implantable devices. PHEA is a biocompatible water‐soluble synthetic polymer, with a protein‐like structure, whose use as a drug carrier and as starting material for many other biomedical and pharmaceutical applications has b…

chemistry.chemical_classificationCloud pointSettore ING-IND/24 - Principi Di Ingegneria ChimicaMaterials scienceBiocompatibilityPolymer-Settore ING-IND/22 - Scienza E Tecnologia Dei MaterialiPolymerizationchemistryTissue engineeringChemical engineeringCopolymerPolymer blendDrug carrierBiomedical engineering
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