Search results for "coating"

showing 10 items of 2834 documents

Basic kinetic model for the reaction yielding linear polyurethanes. II

1995

On the basis of the gradual polyaddition kinetic model developed earlier, an attempt was made to provide a generalized mathematical model for the set of reactions yielding linear polyurethanes. The model is a system of first-order ordinary differential equations. It was assumed at the present stage of this model that the rate constants for the reaction considered do not change. The model developed was then solved numerically. Average molecular weight of the polymer and composition data for oligomers were calculated for a constant volume batch reactor and varied process parameters. The GPC method, which was tested for model urethane oligomers, was employed to verify the model developed. The …

chemistry.chemical_classificationPolymers and PlasticsBasis (linear algebra)Batch reactorThermodynamicsGeneral ChemistryPolymerSurfaces Coatings and FilmsReaction rate constantchemistryChain (algebraic topology)Ordinary differential equationPolymer chemistryMaterials ChemistryMolar mass distributionConstant (mathematics)Journal of Applied Polymer Science
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Crystallization of polymer melts under fast cooling. II. High-purity iPP

1992

SYNOPSIS Samples of a high-purity isotactic polypropylene (iPP) were quenched from the melt so as to monitor cooling history. A continuous variation of morphology and crystal structure was obtained with cooling rate. This is discussed in relation to sample thermal history evidencing that cooling history relevant to quenched samples is in the neighborhood of 90°C. In particular the samples are essentially mesomorphic when at this temperature cooling rates larger than 80°C/s were adopted, while below a few tens of °C/s only a­ monocline form is obtained. Densities of quenched samples were compared with predictions of an isokinetic extrapolation of Avrami model of polymer crystallization kinet…

chemistry.chemical_classificationPolymers and PlasticsChemistryCrystallization of polymersKineticsThermodynamicsGeneral ChemistryPolymerCrystal structureSurfaces Coatings and Filmslaw.inventionMonoclinelawTacticityThermalPolymer chemistryMaterials ChemistryCrystallizationJournal of Applied Polymer Science
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Nonionic Maleic Surfmers

2002

ABSTRACT A set of nonionic maleic surfactants have been prepared, all coming from the derivatization of maleic hemiesters with a long alkyl chain. They are either amidoesters or diester products. In the case of amidoesters, the acid group was first activated and then reacted with primary or secondary or tertiary ethanolamine compounds. In the case of diesters, the hemiester was reacted directly with glycidol, in acid or basic conditions. These surfactants were characterized for their structure by 1H NMR, and for their surface active properties, by surface tension measurements. They were also used in batch emulsion polymerisation of styrene, and seeded core-shell copolymerisation of a 1/1 mi…

chemistry.chemical_classificationPolymers and PlasticsChemistryGlycidolEmulsion polymerizationSurfaces Coatings and FilmsStyreneSurface tensionchemistry.chemical_compoundMonomerEthanolaminePolymer chemistryOrganic chemistryPhysical and Theoretical ChemistryDerivatizationAlkylJournal of Dispersion Science and Technology
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Reactions of Maleisomides with Alcohols

2004

Abstract New surfactants (surfmers) with various amide and ester groups next to C˭C double bonds have been obtained. Maleic acid amidesters (AE) with different hydrophobic groups at the nitrogen atom and hydrophilic substituents at oxygen atoms were synthesized starting with maleic isoimides. 1H KMR and IR spectra were used for their characterization. Some were further characterized for their critical micellar concentration (CMC). A few cationic and zwitterionic surfmers were also prepared from isoimide precursors and characterized. All these surfmers were applied in batch emulsion polymerization of styrene, and in core‐shell seeded copolymerization of styrene and butylacrylate to give late…

chemistry.chemical_classificationPolymers and PlasticsDouble bondMaleic acidCationic polymerizationEmulsion polymerizationSurfaces Coatings and FilmsStyrenechemistry.chemical_compoundchemistryAmideCritical micelle concentrationPolymer chemistryCopolymerOrganic chemistryPhysical and Theoretical ChemistryJournal of Dispersion Science and Technology
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Polymer supported synthesis of mixed ligand complexes

2003

A series of novel polymer-supported mixed ligand complexes were synthesized and studied. Two percent divinyl benzene (DVB)-crosslinked polystyrene supports were synthesized by the suspension copolymerization technique. An ethylene diamine group was anchored onto the support and the corresponding copper complexes were prepared. The ligating functions like phthalate, acetate, and oxalate groups were introduced, and mixed ligands complexes were synthesized. The resultant polymer supported mixed ligand complexes were characterized by UV-Vis, IR, and EPR methods. The stability constants dictate the formation of these complexes on polymer support. Spectral results gave information about the struc…

chemistry.chemical_classificationPolymers and PlasticsGeneral ChemistryPolymerOxalateSurfaces Coatings and Filmschemistry.chemical_compoundchemistryStability constants of complexesDiaminePolymer chemistryMaterials ChemistryCopolymerMoleculeCarboxylatePolystyreneJournal of Applied Polymer Science
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On the handedness of helical aggregates of C3 tricarboxamides: a multichiroptical characterization

2015

A complete chiroptical characterization of the supramolecular polymers formed by tricarboxamides (S)-1 and (R)-1 is performed using ECD, VCD and CPL dichroic techniques. The helical aggregates show an intense CPL signal and their absolute P- or M-configuration is assigned with the help of theoretical calculations.

chemistry.chemical_classificationPolymersMetals and AlloysStereoisomerismGeneral ChemistryPolymerDichroic glassAmidesCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCharacterization (materials science)Supramolecular polymersCrystallographychemistryMaterials ChemistryCeramics and CompositesChemical Communications
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Study on compatibilization of polypropylene-liquid crystalline polymer blends

1997

The mechanical properties, melt rheology, and morphology of binary blends comprised of two polypropylene (PP) grades and two liquid crystalline polymers (LCP) have been studied. Compatibilization with polypropylene grafted with maleic anhydride (PP-g-MAH) has been attempted. A moderate increase in the tensile moduli and no enhancements in tensile strength have been revealed. Those findings have been attributed to the morphology of the blends, which is predominantly of the disperse mode. LCP fibers responsible for mechanical reinforcement were only exceptionally evidenced. Discussion of PP-LCP interfacial characteristics with respect to mechanical properties-morphology interrelations allowed…

chemistry.chemical_classificationPolypropyleneMaterials sciencePolymers and PlasticsMaleic anhydrideGeneral ChemistryPolymerCompatibilizationSurfaces Coatings and Filmschemistry.chemical_compoundchemistryRheologyLiquid crystalUltimate tensile strengthPolymer chemistryMaterials ChemistryPolymer blendComposite materialJournal of Applied Polymer Science
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Aqueous Laponite Clay Dispersions in the Presence of Poly(ethylene oxide) or Poly(propylene oxide) Oligomers and their Triblock Copolymers

2008

The effect of polyethylene oxide (PEO) or polypropylene oxide (PPO) oligomers of various molecular weight (Mw) as well as of triblock copolymers, based on PEO and PPO blocks, on aqueous laponite RD suspensions was studied with small-angle neutron scattering (SANS). The radius of gyration (RG) increases for low Mw whereas the opposite occurs for larger Mw. This behavior is explained on the-basis that an effective RG is given by two contributions: (1) the size of the particles coated with the polymer and (2) the interactions between the laponite RD particles which are attractive for small and repulsive for large polymers. The SANS curves in the whole Q-range are well described by a model of n…

chemistry.chemical_classificationPolypropylenePoly(propylene oxide)Materials scienceAqueous solutiontechnology industry and agricultureOxidemacromolecular substancesPolymerSurfaces Coatings and Filmschemistry.chemical_compoundViscositychemistryPolymer chemistryMaterials ChemistryCopolymerLaponite gels polymer SANS viscosityPhysical and Theoretical ChemistryPoly ethylene
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Improving the properties of polypropylene–wood flour composites by utilization of maleated adhesion promoters

2007

Polymer composites filled with natural organic fillers have gained a significant interest during the last few years, because of several advantages they can offer compared with properties of inorganic-mineral fillers. However, these composites (based, in most cases, on polyolefins) often show a reduction in some mechanical properties. This is mainly due to the problems regarding dispersion of the polar filler particles in the non-polar polymer matrix and their interfacial adhesion with polymer chains. In this work, polypropylene-wood flour composites were prepared and the effect of the addition of a maleated polypropylene was investigated. The two materials were compounded by an industrial c…

chemistry.chemical_classificationPolypropyleneWaxMaterials scienceGeneral Physics and AstronomyWood flourInterfacial adhesionPolymerengineering.materialSurfaces Coatings and FilmsNatural fibers Fibers natural fibrechemistry.chemical_compoundchemistryvisual_artFiller (materials)Ultimate tensile strengthCeramics and Compositesvisual_art.visual_art_mediumengineeringComposite materialDispersion (chemistry)Composite Interfaces
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Anisotropic Stick-slip friction of highly oriented thin films of poly(tetrafluoroethylene) at the molecular level

1996

Lateral force microscopy (LFM) studies of poly(tetrafluoroethylene) (PTFE) films with molecular resolution are reported. Thin PTFE layers with a high degree of orientation were obtained by pressing and sliding a block of polymer on a clean, heated muscovite mica substrate. LFM nanographs obtained on these films by scanning at directions between ca. 40 and 90° with respect to the film orientation direction, i.e. with respect to the direction of the polymer chains, showed a “stick-slip” type frictional motion of the LFM probe tip at the molecular level. The friction force observed at constant load decreased with decreasing scan angles. Chain-chain packing distances obtained by LFM and contact…

chemistry.chemical_classificationPressingMaterials scienceMechanical EngineeringMuscoviteNanotechnologySurfaces and InterfacesPolymerSlip (materials science)engineering.materialSurfaces Coatings and Filmschemistry.chemical_compoundchemistryMechanics of MaterialsMicroscopyengineeringTetrafluoroethyleneComposite materialThin filmAnisotropyTribology letters
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