Search results for "Polymerization"

showing 10 items of 1689 documents

1982

chemistry.chemical_classificationPotassiumInorganic chemistrychemistry.chemical_elementchemistry.chemical_compoundAnionic addition polymerizationchemistryPolymer chemistryLithiumCounterionMethyl methacrylateIonic polymerizationTetrahydrofuranLiving anionic polymerizationDie Makromolekulare Chemie, Rapid Communications
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Pleiotropic Role of Recombinant Silaffin-Like Cationic Polypeptide P5S3: Peptide-Induced Silicic Acid Stabilization, Silica Formation and Inhibition …

2016

Silica-mineralizing organisms such as diatoms manage several aspects of silica chemistry when polymerizing monomeric silicic acid into amorphous silica. Silicic acid is undersaturated in the diatoms’ habitats and mechanisms of enrichment and prevention of uncontrolled mineralization are not well understood. Diatom-biosilica is associated with organic compounds, including polycationic, post-translationally modified peptides termed silaffins, which induce the condensation of silicic acid under supersaturated conditions. Here, we report the pleiotropic action of the designed silaffin-like peptide P5S3, which (i) stabilizes 4–8x silicic acid (in supersaturated conditions of 8.3 mm), (ii) decele…

chemistry.chemical_classificationPrecipitation (chemistry)Inorganic chemistryCationic polymerizationPeptide02 engineering and technologyGeneral Chemistryrespiratory system010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAmino acidchemistry.chemical_compoundHydrolysischemistryBiomimetic synthesisPolymer chemistrySilicic acid0210 nano-technologyDissolutionChemistrySelect
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Controlled cleavage of KLH1 and KLH2 by the V8 protease from Staphylococcus aureus reassociation, electrophoretic and transmission electron microscop…

1999

The reassociation behaviour of protease V8-cleaved peptides from KLH1 and KLH2, the two hemocyanin isoforms from the giant keyhole limpet Megathura crenulata, has been studied by transmission electron microscopy of negatively stained specimens and SDS/PAGE. Reassociation of the complete mixture of protease cleavage products and of combinations of peptide fragments purified by HPLC was performed in the presence of 100 mm CaCl2 and 100 mm MgCl2 at pH 7.4, over a period of 1 to 4 weeks. The V8 protease splits KLH1 into peptide fragments containing the functional units abc, def, defg, defgh, g and h. This mixture of peptide fragments reassociated to form helical tubular polymers, with a diamete…

chemistry.chemical_classificationProteasebiologyStereochemistrymedicine.medical_treatmentProtein subunitHydrolysisSerine EndopeptidasesHemocyaninPeptideMegathura crenulatabiology.organism_classificationCleavage (embryo)BiochemistryPeptide FragmentsMicroscopy ElectronBiochemistrychemistryPolymerizationHemocyaninsmedicineProtein IsoformsElectrophoresis Polyacrylamide GelPolyacrylamide gel electrophoresisEuropean journal of biochemistry
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Mean square radius of gyration and hydrodynamic radius of jointed star (dumbbell) and H-comb polymers

1996

Equations for the mean square radius of gyration and the hydrodynamic radius for jointed stars (dumbbells) and H-combs are derived, based on random flight statistics for each subchain. Comparision with literature data on computer simulations and experimental data for H-combs show good agreement for the g-value of the mean square radius of gyration even in good solvents. This suggests that for the mean square radius of gyration the relative dimension of a H-comb relative to the linear molecule of the same degree of polymerization is not altered significantly by long range interactions, as in the case of star polymers. For the hydrodynamic radius the situation is different. Fair agreement is …

chemistry.chemical_classificationQuantitative Biology::BiomoleculesHydrodynamic radiusPolymers and Plasticsbusiness.industryChemistryOrganic ChemistryLinear molecular geometryPolymerDegree of polymerizationCondensed Matter PhysicsRelative dimensionMolecular physicsCondensed Matter::Soft Condensed MatterInorganic ChemistryViscosityOpticsMaterials ChemistryRadius of gyrationDumbbellbusinessMacromolecular Theory and Simulations
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Kinetic Monte Carlo Simulations of Flow-Assisted Polymerization

2012

We performed kinetic Monte Carlo simulations on a model of a polymerization process in the presence of a periodic oscillatory flow to explore the role of mixing in polymerization reactors. Application of an oscillatory flow field helps overcome the diffusive limitations that develop during a polymerization process due to an increase in the molecular weights of polymer chains, thereby giving rise to high rates of polymerization. A systematic increase in the flow strength results in a "dynamic" coil-stretch transition, leading to an elongation of polymer chains. Reactive ends of stretched (polymer) chains react more frequently than the reactive ends of coiled chains, which are screened by oth…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials sciencePolymers and PlasticsField (physics)Organic Chemistrytechnology industry and agricultureMixing (process engineering)NanotechnologyPolymerInorganic Chemistrychemistry.chemical_compoundMonomerchemistryPolymerizationFlow (mathematics)Chemical physicsMaterials ChemistryKinetic Monte CarloChoked flowACS Macro Letters
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Frictional drag between polymer bearing surfaces

2002

Some fundamental features of friction between two polymer bearing surfaces in relative sliding motion are investigated by molecular dynamics simulations. End-tethered and adsorbed polymers are considered under good and poor solvent conditions. The shear stress is measured while varying the solvent's viscosity, surface separation, degree of polymerization and grafting density. For all systems we observe shear thinning that is attributed to the orientation of the chains along the shear direction. This effect is particularly strong for brushes, for which the shear stress during the steady sliding state is mainly determined by the degree of overlap between the brushes.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceShear thinningGeneral Physics and AstronomyPolymerDegree of polymerizationPhysics::Fluid DynamicsCondensed Matter::Soft Condensed MatterMolecular dynamicsClassical mechanicsAdsorptionShear (geology)chemistryHardware and ArchitectureDragShear stressComposite materialComputer Physics Communications
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Pressure-Induced Formation of Diblock Copolymer "Micelles" in Supercritical Fluids. A Combined Study by Small Angle Scattering Experiments and Mean-F…

2004

We developed a simple mean-field theory to describe polymer and AB diblock copolymer phase separation in supercritical (SC) fluids. The highly compressible SC fluid has been described by using a phenomenological hole theory, properly extended to consider the solvent/polymer/vacancy pseudoternary mixture. The model has been applied to describe the phase behavior of AB-diblock copolymers under the assumption of a strong solvent selectivity for just one copolymer chain. In our model the solvent selectivity is a strong function of the external pressure because in compressible fluids vacancies reduce the number of favorable solvent-polymer contacts. The combined effect of the pressure on the ave…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceSmall-angle X-ray scatteringGeneral Physics and AstronomyThermodynamicsPolymerSupercritical fluid extraction Carbon dioxide dispersion polymerizationSupercritical fluidCondensed Matter::Soft Condensed MatterMean field theorychemistryPhase (matter)CopolymerOrganic chemistryPolymer blendPhysical and Theoretical ChemistrySolvent effects
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A Unified Theory of Liquid-Liquid Demixing and Polymer Formation Kinetics

2009

Sickle hemoglobin is a natural hemoglobin mutation with a hydrophobic replacement of a charged aminoacid on the molecular surface. This leads to aggregation into rigid helical structures (“polymerization”), the underlying cause of sickle cell disease. It has also been shown that polymerization occurs in close correspondence with the phase transition of liquid-liquid demixing , or with the critically diverging fluctuations of local concentration occurring in its proximity. Due to this correspondence, polymerization kinetics remarkably appear to exhibit, with respect to demixing temperature, the same universal scaling features shown by amplitudes and lifetimes of fluctuations occurring in pro…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesPhase transitionChemistryKineticsBiophysicsPolymerLight scatteringlaw.inventionCrystallographyPolymerizationlawChemical physicsCrystallizationUnified field theoryScalingBiophysical Journal
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Studies of network organization and dynamics of e-beam crosslinked PVPs: From macro to nano

2012

Abstract In this work the influence of poly(N-vinyl pyrrolidone) (PVP) concentration in water on the organization and dynamics of the corresponding macro-/nanogel networks has been systematically investigated. Irradiation has been performed at the same irradiation dose (within the sterilization dose range) and dose rate. In the selected irradiation conditions, the transition between macroscopic gelation and micro-/nanogels formation is observed just below the critical overlap concentration (∼1 wt%), whereas the net prevalence of intra-molecular over inter-molecular crosslinking occurs at a lower polymer concentration (below 0.25 wt%). Dynamic–mechanical spectroscopy has been applied as a cl…

chemistry.chemical_classificationRadiationMaterials scienceAqueous solutionNMR spin–lattice relaxationSpin–lattice relaxationNanogelsPolymerDynamic mechanical analysise-Beam irradiation; PVP aqueous solutions; Nanogels; Dynamic mechanical spectroscopy; NMR spin–lattice relaxationDynamic mechanical spectroscopyNanogelPVP aqueous solutionsPolymerizationChemical engineeringchemistryNano-Polymer chemistrye-Beam irradiationElectron beam processingPVP aqueous solutionSettore CHIM/07 - Fondamenti Chimici Delle TecnologieNMR spin-lattice relaxationNanogelRadiation Physics and Chemistry
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Carboxylation of a linear low density polyethylene via gamma irradiation in presence of carbon dioxide in subcritical and supercritical conditions

1994

Abstract In this work the molecular modifications induced in a linear low density polyethylene gamma irradiated in presence of carbon dioxide both in subcritical and supercritical conditions are presented. The obtained results indicate that this process can be a new and interesting way in order to graft oxidized groups in the polyethylene chains. Moreover it is worth noting that, together with these functionalization reactions, also a significant crosslinking occurs, with improvement in some mechanical tensile behaviour.

chemistry.chemical_classificationRadiationMaterials sciencePolymerPolyethyleneSupercritical fluidLinear low-density polyethylenechemistry.chemical_compoundchemistryPolymerizationCarboxylationChemical engineeringCarbon dioxideCompounds of carbonNuclear chemistryRadiation Physics and Chemistry
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