Search results for "Solvent"

showing 10 items of 1395 documents

Living Polymer Chains with Predictable Molecular Weight and Dispersity via Carbanionic Polymerization in Continuous Flow: Mixing Rate as a Key Parame…

2016

Aiming at systematic variation of the parameter dispersity, Đ (or “polydispersity”), living polymers with predictable dispersity (Đ = 1.15–2.20) and controlled molecular weights (Mn = 3200–18 500 g mol–1) were prepared via carbanionic polymerization. The approach relies on a continuous flow reactor equipped with a tangential four-way jet micromixing device. By varying the total flow rate, the mixing efficiency of the initiator (sec-BuLi) and the corresponding vinyl monomers is controlled, resulting in polymers with predefined dispersity, while the number-average molecular weight, Mn, is kept constant. In this manner living polystyrene (PS), poly(p-methylstyrene) (PpMeS), and poly(2-vinylpyr…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryDispersity02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesMicromixingInorganic ChemistryHexaneSolventchemistry.chemical_compoundMonomerPolymerizationchemistryChemical engineeringPolymer chemistryMaterials ChemistryPolystyrene0210 nano-technologyMacromolecules
researchProduct

Excess viscosity and glass transition

2001

Abstract Literature data on the viscosity of solutions of poly(butyl methacrylate) (PBMA) and poly(methyl methacrylate) (PMMA) in diethyl phthalate (DEP) for different temperatures, including the range around and below T g , the glass transition temperatures of the pure polymers, were evaluated by means of an approach that uses surface fractions as composition variables. The discussion of these results together with information on solutions of the isomeric polymers, poly(vinyl acetate) (PVAc) and poly(methyl acrylate) (PM(A)), in the same solvent testifies that the previously published relations remain valid for T T g . They enable the determination of viscosities of the pure polymers below…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryThermodynamicsConcentration effectPolymerSolventchemistry.chemical_compoundViscositychemistryPolymer chemistryMaterials ChemistryVinyl acetateMethyl methacrylateMethyl acrylateGlass transitionPolymer
researchProduct

Role of Solvent Compatibility in the Phase Behavior of Binary Solutions of Weakly Associating Multivalent Polymers

2021

AbstractCondensate formation of biopolymer solutions, prominently those of various intrinsically disordered proteins (IDPs), is determined by “sticky” interactions between associating residues, multivalently present along the polymer backbone. Using a ternary mean field “stickers-and-spacers” model, we demonstrate that if sticker association is of the order of a few times the thermal energy, a delicate balance between specific binding and non-specific polymer-solvent interactions gives rise to a particularly rich ternary phase behavior under physiological circumstances. For a generic system represented by a solution comprising multi-associative scaffold and client polymers, the difference i…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsPolymersBioengineeringPolymerIntrinsically disordered proteinsMiscibilityIsothermal processArticleBiomaterialsIntrinsically Disordered ProteinschemistryMean field theoryChemical physicsPhase (matter)Materials ChemistrySolventsHumansTernary operationPhase diagram
researchProduct

Interpolymer complexes and polymer compatibility.

2012

A reliable method to decide whether two polymers A and B are miscible or incompatible would be very helpful in many ways. In this contribution we demonstrate why traditional procedures cannot work. We propose to use the intrinsic viscosities [η] of the polymer blends instead of the composition dependence of the viscosities as a criterion for polymer miscibility. Two macromolecules A and B are miscible because of sufficiently favorable interactions between the two types of polymer segments. For solutions of these polymers in a joint solvent, this Gibbs energetic preference of dissimilar intersegmental contacts should prevail upon dilution and lead to the formation of interpolymer complexes, …

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsPolymersViscosityIntrinsic viscosityOrganic ChemistryThermodynamicsWaterDextransDimethylformamidePolymerMiscibilityDilutionSolventchemistryPolysaccharidesCompatibility (mechanics)Polymer chemistryMaterials ChemistryPolystyrenesPolyvinylsPolymer blendGlucansMacromoleculeMacromolecular rapid communications
researchProduct

Grafted polymer layers under variable solvent conditions: A Monte Carlo simulation

1993

Polymer chains anchored with one end at a hard wall under variable solvent conditions are investigated by Monte Carlo simulations using the bond- fluctuation model. Detail information on the structural properties are obtained above, at, and below the Θ-point and discussed in terms of the appropriate theories. In particular, the scaling of the brush thickness is formulated and verified by the simulation data. For the dynamics at the Θ-point, both the relaxation time of the chain configuration and the mean-square time displacement are studied. At temperatures distinctly below the Θ-point, we find that the layer develops considerable lateral inhomogeneity in its density, which has not been pre…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsTime displacementOrganic ChemistryMonte Carlo methodMechanicsPolymerCondensed Matter PhysicsSolventChain (algebraic topology)chemistryMaterials ChemistryStatistical physicsScalingVariable (mathematics)Makromolekulare Chemie. Macromolecular Symposia
researchProduct

Isobornyl Methacrylate as a Reactive Solvent of Polyethylene

2004

Solutions containing 15 wt, -% of a low-molar-mass polyethylene (PE) in isobornyl methacrylate (IBoMA), containing 0, 5 or 10 wt.-% of 1,4 butanediol dimethacrylate (BDDMA) as crosslinker, were polymerized using either benzoyl peroxide (BPO), at 80°C, or dicumyl peroxide (DCPO), with a thermal cycle attaining 150°C, as initiators. Phase separation of an amorphous PE-rich phase took place when carrying out the reaction at temperatures higher than the PE melting temperature. Partial crystallization of PE was observed when cooling to room temperature. Depending on the initial amount of BDDMA, the fraction of PE that was phase separated varied between 57 and 66% of the initial amount, with crys…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsVapor pressureGeneral Chemical EngineeringOrganic ChemistryBenzoyl peroxidePolymerPolyethylenelaw.inventionSolventchemistry.chemical_compoundChemical engineeringchemistryPolymerizationlawPolymer chemistryMaterials ChemistrymedicineCrystallizationGlass transitionmedicine.drugMacromolecular Materials and Engineering
researchProduct

Polymer, Metal, and Hybrid Nano- and Mesotubes by Coating Degradable Polymer Template Fibers (TUFT Process)

2000

). Selective reaction with the silver atoms at the interface of the particles occurred and the coated particles were then extracted from reverse micelles. The powder of coated nanocrystals thus obtained was then dispersed in hexane, giving an optically clear solution. The size distribution was still rather large (30 %), and to reduce it a size-selected precipitation process [20] was used. In this process two solvents, such as hexane and pyridine, are mixed. The first is a good solvent and the second a poor solvent for the alkyl chains. With this solvent mixture, the larger coated particles flocculated whereas the smaller ones remain in the solution, thus providing size selection. By repeati…

chemistry.chemical_classificationMaterials sciencePrecipitation (chemistry)Mechanical EngineeringPolymerengineering.materialMicelleHexaneSolventchemistry.chemical_compoundchemistryCoatingNanocrystalChemical engineeringMechanics of MaterialsPolymer chemistryengineeringGeneral Materials ScienceAlkylAdvanced Materials
researchProduct

Biological evaluation of PLLA membranes, with different pore diameters, to stimulate cell adhesion and growth in vitro

2015

Polymeric membranes prepared via DIPS (Diffusion Induced Phase Separation) are widely studied and utilized as scaffolds for the regeneration of tissue. In this work, poly (L)-lactide membrane are prepared through a DIPS protocol starting from a ternary solution made of polymer, dioxane (solvent) and water (non-solvent). A three-dimensional, porous and mechanically stable membrane is desirable for ingrowth of human bronchial epithelial cells. Polymeric membranes prepared via DIPS (Diffusion Induced Phase Separation) are widely studied and utilized as scaffolds for the regeneration of tissue. In this work, poly (L)-lactide membrane are prepared through a DIPS protocol starting from a ternary …

chemistry.chemical_classificationMaterials scienceRegeneration (biology)DiffusionPhase separationtechnology industry and agriculturepolymeric MembranePolymerPLLASolventPhysics and Astronomy (all)MembranechemistryChemical engineeringPolymer chemistryCell AdhesionCell adhesionTernary operationPorosityAIP Conference Proceedings
researchProduct

Structure of bottle-brush brushes under good solvent conditions: a molecular dynamics study.

2011

We report a simulation study for bottle-brush polymers grafted on a rigid backbone. Using a standard coarse-grained bead-spring model extensive molecular dynamics simulations for such macromolecules under good solvent conditions are performed. We consider a broad range of parameters and present numerical results for the monomer density profile, density of the untethered ends of the grafted flexible backbones and the correlation function describing the range that neighboring grafted bottle-brushes are affected by the presence of the others due to the excluded volume interactions. The end beads of the flexible backbones of the grafted bottle-brushes do not access the region close to the rigid…

chemistry.chemical_classificationMaterials scienceStatistical Mechanics (cond-mat.stat-mech)PolymersMolecular ConformationFOS: Physical sciencesPolymerCondensed Matter - Soft Condensed MatterMolecular Dynamics SimulationCondensed Matter PhysicsSolventMolecular dynamicsCorrelation function (statistical mechanics)chemistry.chemical_compoundMonomerchemistryChemical physicsExcluded volumeSide chainSolventsSoft Condensed Matter (cond-mat.soft)Quantum TheoryGeneral Materials ScienceCondensed Matter - Statistical MechanicsMacromoleculeJournal of physics. Condensed matter : an Institute of Physics journal
researchProduct

Industrial applications of the aggregation of block copolymers in supercritical CO 2 : a SANS study

2002

Industrial applications of supercritical carbon dioxide (scCO2) rely upon the rather selective and easily adjustable solvent ability of CO2. CO2 near the critical point is a poor solvent for high molecular weight (HMW) hydrocarbon polymers, while it is a very good solvent for amorphous fluorinated polymers. By increasing the pressure, CO2 becomes a good solvent even for HMW hydrogenated chains. Specially engineered amphiphilic di-block copolymers, with CO2-philic and CO2-phobic portions, are expected to undergo trough a monomer–aggregate transition when the solvent density of the scCO2 changes. Here small-angle neutron scattering (SANS) results are reported for a block copolymer dissolved i…

chemistry.chemical_classificationMaterials scienceSupercritical carbon dioxideGeneral ChemistryPolymerNeutron scatteringSupercritical fluidSolventHydrocarbonchemistryChemical engineeringAmphiphilePolymer chemistryCopolymerGeneral Materials ScienceApplied Physics A: Materials Science & Processing
researchProduct