Search results for "polymerization"

showing 10 items of 1689 documents

Entanglement Transition in Hyperbranched Polyether-Polyols

2010

Are hyperbranched polymers capable of forming entanglements? This is the central issue of this contribution. Hyperbranched polyglycerol (hbPG) samples with different molecular weights (600-106 000 g · mol(-1) ), narrow polydispersities (1.2-1.8) and high degrees of branching (≈0.6) were prepared by anionic ring-opening polymerization. The viscoelastic properties of these polymers with respect to molecular architecture and molar mass were investigated. At low molecular weights "classical" scaling behavior between zero shear viscosity and molecular weight can be observed, whereas between 3 000 and 10 000 g · mol(-1) a plateau-like area is found. The results indicate entanglement dynamics when…

chemistry.chemical_classificationMolar massPolymers and PlasticsMolecular massOrganic ChemistryThermodynamicsPolymerBranching (polymer chemistry)ViscoelasticitychemistryRheologyPolymerizationPolymer chemistryMaterials ChemistryScalingMacromolecular Rapid Communications
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Experimental design approach in the synthesis of molecularly imprinted polymers specific for iprodione fungicide

2015

International audience; An experimental design (ED) approach was applied to study the weight of three factors in the synthesis of a molecularly imprinted polymer (MIP) specific for iprodione fungicide. The objective was to obtain a high specific polymer with the best performance of iprodione binding. Thirteen iprodione-imprinted polymers and 13 non-imprinted polymers (NIP) were synthesized according to ED having 3 influencing factors: the polymerization method, the crosslinker nature and the functional monomer type. For each factor, two levels were studied: bulk and precipitation polymerization for the first factor, trimethylolpropane trimethacrylate (TRIM) and ethylene glycol dimethacrylat…

chemistry.chemical_classificationMolecularly imprinted polymerIprodionePolymers and PlasticsGeneral Chemical EngineeringEthylene glycol dimethacrylateFungicideMolecularly imprinted polymerWineGeneral ChemistryPolymerBiochemistryExperimental designchemistry.chemical_compoundchemistryPolymerizationSpecific surface areaPolymer chemistryMaterials ChemistryPrecipitation polymerizationEnvironmental ChemistryMethacrylamide[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologySolid phase extractionNuclear chemistry
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Functional end groups for polymers prepared using ring-opening metathesis polymerization.

2011

The precise placement of functional groups on the chain-ends of macromolecules is a major focus of polymer research. Most common living polymerization techniques offer specific methods of end-functionalization governed by the active propagating species and the kinetics of the polymerization reaction. Ring-opening metathesis polymerization has established itself as one of the most functional-group-tolerant living polymerization techniques known, but this tolerance has limited the number of available functionalization reactions. Metathesis chemists have therefore been required to develop a variety of end-functionalizations, adapting each of them to the reactivity scheme of the particular cata…

chemistry.chemical_classificationMolybdenumPolymer scienceMolecular StructureMacromolecular SubstancesPolymersGeneral Chemical EngineeringGeneral ChemistryPolymerMetathesisCatalysisRutheniumchemistryPolymerizationOrganometallic CompoundsSurface modificationLiving polymerizationRing-opening metathesis polymerisationReactivity (chemistry)MacromoleculeNature chemistry
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Cooperative formation of inorganic-organic interfaces in the synthesis of silicate mesostructures.

1993

A model is presented to explain the formation and morphologies of surfactant-silicate mesostructures. Three processes are identified: multidentate binding of silicate oligomers to the cationic surfactant, preferential silicate polymerization in the interface region, and charge density matching between the surfactant and the silicate. The model explains present experimental data, including the transformation between lamellar and hexagonal mesophases, and provides a guide for predicting conditions that favor the formation of lamellar, hexagonal, or cubic mesostructures. Model Q(230) proposed by Mariani and his co-workers satisfactorily fits the x-ray data collected on the cubic mesostructure …

chemistry.chemical_classificationMultidisciplinaryCationic polymerizationMineralogyMesophasePolymerSilicatechemistry.chemical_compoundPulmonary surfactantchemistryPolymerizationChemical engineeringddc:540Lamellar structureGyroidScience (New York, N.Y.)
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Synthesis, Morphology and Rheological Behavior of Fluoropolymer-Polyacrylate Nanocomposites

2007

Nanocomposite materials composed of a PTFE copolymer core and an acrylic copolymer shell have been prepared by seeded emulsion polymerization. The effect of seed particle number and shell polymer composition on secondary particle nucleation and film formation ability of the dispersions has been studied. While TEM reveals a core-shell structure present in the particles, AFM investigation of the film shows a nearly uniform dispersion of the fluorinated seed particles in a matrix formed by the shell polymer. Rheological measurements show composite behavior of the core-shell latex films, especially at elevated temperatures, and an increase in viscosity and storage modulus when compared with the…

chemistry.chemical_classificationNanocompositeMaterials sciencePolymers and PlasticsGeneral Chemical EngineeringComposite numberEmulsion polymerizationGeneral ChemistryPolymerDynamic mechanical analysischemistry.chemical_compoundchemistryPolymer chemistryCopolymerFluoropolymerComposite materialDispersion (chemistry)Macromolecular Reaction Engineering
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Optically active amphiphilic hyperbranched polyglycerols as templates for palladium nanoparticles

2006

Abstract We report a systematic study on the encapsulation of palladium nanoparticles in optically active amphiphilic hyperbranched polyglycerols with different optical signs and different degrees of polymerization, namely (−)-P(G 40 C16 0.5 ) 1 and (+)-P(G 73 C16 0.5 ) 2 . Several issues have been addressed here: (a) relatively wide size distributions (1–5 nm) of palladium nanoparticles have been achieved, (b) a remarkable template effect ( 1 , DP n  = 40, 1.2 ± 0.1 nm; 2 , DP n  = 73, 2.3 ± 0.1 nm average particle size) has been observed using TEM technique, as shown by the particle size dependent on the degree of polymerization of the polymers, (c) NaBH 4 is found to be a convenient redu…

chemistry.chemical_classificationNanoparticlechemistry.chemical_elementPolymerDegree of polymerizationInorganic ChemistrychemistryPolymerizationHeck reactionPolymer chemistryMaterials ChemistryParticle sizePhysical and Theoretical ChemistryTrifluoromethanesulfonatePalladiumInorganica Chimica Acta
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Living Light-Induced Crystallization-Driven Self-Assembly for Rapid Preparation of Semiconducting Nanofibers.

2018

Well-defined nanostructures composed of conjugated polymers have attracted significant attention due to their intriguing electronic and optical properties. However, precise control of the size and uniformity of these semiconducting nanostructures is still rare and challenging, despite recent advances in strategies to obtain self-assembled nanostructures with narrow dispersions. Herein, we demonstrate the preparation of fluorescent conjugated block copolymers by one-shot polymerization and rapid formation of nanofibers in a few minutes via light-induced crystallization-driven self-assembly, driven by facile cis-to- trans photoisomerization of its poly( p-phenylenevinylene) blocks. Furthermor…

chemistry.chemical_classificationNanostructurePhotoisomerizationNanotechnology02 engineering and technologyGeneral ChemistryPolymerConjugated system010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistryCatalysis0104 chemical sciencesColloid and Surface ChemistryPolymerizationchemistryNanofiberCopolymerSelf-assembly0210 nano-technologyJournal of the American Chemical Society
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Contribution of Protein Flexibility to the Foaming Properties of Casein

1990

The effect of biopolymer flexibility on the foaming properties of casein was investigated. Flexibility was altered by: (1) chemical modification (covalent binding of a monosaccharide on the lysyl residues) or (2) pH change. Electron Spin Resonance was used to measure the reorientational frequency of casein residues labeled with nitroxide radicals. High levels of glycosylation induced increased protein flexibility and improved the foaming capacity. Good agreement was observed between higher values of flexibility and improved surface properties near the isoelectric point.

chemistry.chemical_classificationNitroxide mediated radical polymerizationGlycosylationFlexibility (anatomy)Chemical modificationengineering.materialchemistry.chemical_compoundmedicine.anatomical_structureIsoelectric pointChemical engineeringchemistryCaseinengineeringmedicineOrganic chemistryMonosaccharideBiopolymerFood ScienceJournal of Food Science
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Grafting of polymer chains on the surface of carbon nanotubes via nitroxide radical coupling reaction

2015

Poly(butylene succinate) (PBS) was grafted on the surface of TEMPO (2,2,6,6-tetramethyl-1-piperidinyloxy) modified multi-walled carbon nanotubes (MWCNTs) via a nitroxide radical coupling reaction. TEMPO functionalized MWCNTs (MWCNTs-g-TEMPO) were synthesized using the Cu(I)-catalyzed azide/alkyne click chemistry approach and the covalent bond of the nitroxide moieties onto the MWCNTs was confirmed via electron paramagnetic resonance (EPR) spectroscopy. The PBS grafting on the sidewalls of MWCNTs was carried out in solution via peroxide-induced formation of macroradicals and it was confirmed by EPR and attenuated total reflectance Fourier transform infrared analysis. Preliminary rheological …

chemistry.chemical_classificationNitroxide mediated radical polymerizationMaterials sciencePolymers and PlasticsPolymer nanocompositeOrganic ChemistryAlkyne02 engineering and technologyPolymerCarbon nanotube010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceslaw.inventionchemistry.chemical_compoundchemistryCovalent bondlawPolymer chemistryMaterials ChemistryAzide0210 nano-technologyElectron paramagnetic resonancePolymer International
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A new approach for the synthesis of magnetic materials based on nitroxide free radicals and inorganic coordination polymers

2001

The use of nitronyl nitroxide (NN) radicals as spectators inside extended inorganic magnetic lattices is described. Two possibilities are presently being explored, namely, the design of oxalato-bridged bimetallic networks by using cationic NN radicals of the N-alkylpyridinium type as templating agents, and the design of bimetallic lattices based on hexacyanometalates and nickel(II) diaminocomplexes incorporating anionic NN radicals of the carboxyphenyl type.

chemistry.chemical_classificationNitroxide mediated radical polymerizationMolecular magnetsRadicalCationic polymerizationchemistry.chemical_elementPolymerPhotochemistryInorganic ChemistryNickelchemistryMaterials ChemistryPhysical and Theoretical ChemistryBimetallic stripPolyhedron
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