Search results for "Stability"

showing 10 items of 3085 documents

Electro-Hydrodynamic Instabilities in Main Chain Thermotropic Liquid Crystalline Polyesters

1984

Abstract We have investigated the response behavior of the thermotropic nematic polymer, DDA-9, in an electric field. DDA-9 is composed of regularly alternating moieties and flexible spacers. At a critical threshold voltage, dependent on molar mass, these polymers show the onset of instability. The appearance of a (non-fluctuating) striped pattern (Williams domains) is shown and the time of formation and relaxation of these patterns is investigated as a function of applied Voltage.

Polyesterchemistry.chemical_classificationMolar masschemistryChemical physicsLiquid crystalElectric fieldRelaxation (NMR)Polymer chemistryPolymerThermotropic crystalInstabilityMolecular Crystals and Liquid Crystals
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Thermal stability of poly(styrene-b-methyl methacrylate) and poly(styrene-b-ethylene-co-1-butene-b-methyl methacrylate)

1993

The thermal stability of poly(styrene-b-methyl methacrylate) diblock copolymers (= P(S-b-MMA)) and poly(styrene-b-ethylene-co-1-butene-b-methyl methacrylate) triblock copolymers (=P(S-b-EB-b-MMA)) was investigated. Well-defined high molecular weight block copolymers with narrow molecular weight distribution (MWD) were molded at different temperatures in vacuum and the alteration of the MWD was sensitively monitored by gel permeation chromatography (GPC). Up to 240°C P(S-b-MMA) shows almost no broadening of the MWD. At higher temperatures low molecular weight polystyrene-rich portions are formed. The number average molecular weight (Mn) is strongly reduced. P(S-b-EB-b-MMA) triblock copolymer…

Polymers and PlasticsChemistry1-ButeneGeneral ChemistryCondensed Matter PhysicsMethacrylateStyreneGel permeation chromatographychemistry.chemical_compoundPolymer chemistryMaterials ChemistryCopolymerMolar mass distributionThermal stabilityMethyl methacrylatePolymer Bulletin
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Heparin-Based Nanocapsules as Potential Drug Delivery Systems

2015

Herein, the synthesis and characterization of heparin-based nanocapsules (NCs) as potential drug delivery systems is described. For the synthesis of the heparin-based NCs, the versatile method of miniemulsion polymerization at the droplets interface was achieved resulting in narrowly distributed NCs with 180 nm in diameter. Scanning and transmission electron microscopy images showed clearly NC morphology. A highly negative charge density for the heparin-based NCs was determined by measuring the electro-kinetic potential. Measuring the activated clotting time demonstrated the biological intactness of the polymeric shell. The ability of heparin-based NCs to bind to antithrombin (AT III) was i…

Polymers and PlasticsChemistryAnalytical chemistryBioengineeringIsothermal titration calorimetrybehavioral disciplines and activitiesNanocapsulesBiomaterialsMiniemulsionPolymerizationChemical engineeringDynamic light scatteringTransmission electron microscopymental disordersDrug deliveryMaterials ChemistryChemical stabilityBiotechnologyMacromolecular Bioscience
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Kinetic parameters of a cyanate ester resin catalyzed with different proportions of nonylphenol and cobalt acetylacetonate catalyst

2005

The isothermal cure of a dicyanate ester monomer has been investigated by differential scanning calorimetry (DSC) in the presence of different quantities of a catalyst system formed by nonylphenol (NP) and cobalt (II) acetylacetonate (Co(AcAc)2). Two sets of experiences were studied. Firstly, the NP composition was varied from 0 to 10 per hundred resin (phr) and secondly, the Co(AcAc)2 loadings were changed at 2 phr of NP. It has been observed that the cyanate conversion increases significantly after the first addition of the metal catalyst and, also, at the same time the thermal stability improves. Moreover, the kinetic data have been fitted with a second-order equation respect to the cyan…

Polymers and PlasticsChemistryOrganic ChemistryGeneral Physics and Astronomychemistry.chemical_elementActivation energyCyanateCatalysischemistry.chemical_compoundDifferential scanning calorimetryReaction rate constantCyanate esterPolymer chemistryMaterials ChemistryThermal stabilityCobaltNuclear chemistryEuropean Polymer Journal
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Pyrene Containing Polymers for the Non-Covalent Functionalization of Carbon Nanotubes

2009

Pyrene containing diblock copolymers based on poly(methyl methacrylate) were synthesized and investigated regarding their adsorption on carbon nanotubes (CNT). The pyrene units were introduced using a reactive ester monomer for the build up of the second block which later on was reacted polymer-analogously with amine functionalized pyrene derivatives. As we started from the same reactive ester intermediate, full block length identity is given. We varied the length of the anchor block to find an optimal block length and used pyren-1-yl-methylamine as well as 4-pyren-1-yl-butylamine as anchor units. For both anchor units a maximal adsorption was found for 13 and 20 anchor units, respectively.…

Polymers and PlasticsChemistryOrganic ChemistryRadical polymerizationCondensed Matter Physicschemistry.chemical_compoundEnd-groupMonomerAdsorptionPolymer chemistryDispersion stabilityMaterials ChemistryCopolymerPyrenePhysical and Theoretical ChemistryMethyl methacrylateMacromolecular Chemistry and Physics
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Morphology and thermal behavior of dicyanate ester-polyetherimide semi-IPNS cured at different conditions

2000

A high-temperature thermosetting bisphenol-A dicyanate, BADCy was modified with polyetherimide, PEI, at various compositions. Phase separation and rheokinetics through curing were studied by optical microscopy, dynamic and isothermal differential scanning calorimetry, and rheological measurements. The PEI phase separated at the early stages of curing, well before gelation, and did not affect the polycyclotrimerization kinetics. The phase structure and thermal properties of the final network were investigated as a function of the PEI content and cure temperature. For this purpose, dynamic mechanical analysis, scanning electron microscopy studies, and thermogravimetrical analysis were carried…

Polymers and PlasticsChemistrySpinodal decompositionThermosetting polymerGeneral ChemistryDynamic mechanical analysisPolyetherimideIsothermal processSurfaces Coatings and Filmschemistry.chemical_compoundDifferential scanning calorimetryChemical engineeringPolymer chemistryMaterials ChemistryThermal stabilityCuring (chemistry)Journal of Applied Polymer Science
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Sulfur’s role in the flame retardancy of thio-ether–linked hyperbranched polyphosphoesters in epoxy resins

2020

Abstract Hyperbranched polyphosphoesters are promising multifunctional flame retardants for epoxy resins. These polymers were prepared via thiol-ene polyaddition reactions. While key chemical transformations and modes of actions were elucidated, the role of sulfur in the chemical composition remains an open question. In this study, the FR-performance of a series of phosphorus-based flame retardant additives with and without sulfur (thio-ethers or sulfones) in their structure are compared. The successful synthesis of thio-ether or sulfone-containing variants is described and verified by 1H and 31P NMR, also FTIR and MALDI-TOF. A decomposition process is proposed from pyrolytic evolved gas an…

Polymers and PlasticsEvolved gas analysisChemistryOrganic ChemistryGeneral Physics and Astronomychemistry.chemical_elementThio-02 engineering and technologyEpoxy010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesSulfur0104 chemical scienceschemistry.chemical_compoundMonomerChemical engineeringCone calorimetervisual_artMaterials Chemistryvisual_art.visual_art_mediumThermal stability0210 nano-technologyFire retardantEuropean Polymer Journal
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New phosphazene-based chain extenders containing allyl and epoxide groups

2003

In this paper we present the synthesis and the characterization of cyclophosphazenes substituted with allyl groups, their transformation in epoxide-containing cyclophosphazenes and the final utilization of these compounds as chain extenders in combination with polyamides. The reaction at high temperature of Nylon-6 with epoxy-functionalized cyclophosphazenes leads to the opening of the epoxy units by the action of both amino (--NH2) and carboxylic (--COOH) end-groups of the polymer to enhance the final molecular weight of this material. The consequences of this fact on the thermal, mechanical and visco-elastic properties of treated Nylon-6 have been also evaluated and compared to those of t…

Polymers and PlasticsGeneral Chemical EngineeringEpoxidechemistry.chemical_compoundPolymer chemistryMaterials ChemistryOrganic chemistryThermal stabilityPhosphazenechemistry.chemical_classificationchain extensionpolyamideGeneral ChemistryEpoxyPolymerNMREnd-groupSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiNylon 6chemistryvisual_artPolyamidecyclophosphazeneNylon-6; cyclophosphazenes; chain extension; polyamides; NMR.visual_art.visual_art_mediumnylon-6Designed Monomers and Polymers
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Polymorphic domains in monolayers of isomeric triple-chain phospholipids

1991

Monolayers of two isomeric branched chain phosphatidyl cholines at the air/water interface have been studied by means of fluorescence microscopy. The lipids differ in the position of the branched chain at the glycerol backbone and carry three chains per headgroup of almost equal length. Most qualitative features of the compression isotherms are similar except a difference of 4 A2/molecule in the minimum molecular area at high lateral pressures. This indicates a more condensed solid phase of compound C2 and is also reflected in the shapes of domains observed in the LE/LC phase coexistence range: domains with sharp edges and a mostly hexagonal shape are formed. On the other hand, the compound…

Polymers and PlasticsHexagonal crystal systemChemistryOrganic ChemistryLimitingCondensed Matter PhysicsInstabilityCrystallographyChain (algebraic topology)Phosphatidyl CholinesPhase (matter)MonolayerMaterials ChemistryMoleculeMakromolekulare Chemie. Macromolecular Symposia
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Spectroscopic Studies of Oligonucleotide Adducts and Base Sequence Preference of Adducts Formed by the Stereoisomers of 7,8-Dihydroxy-9,10-epoxy-7,8,…

1996

Abstract 5′-d(CCTATAGATATCC) has been reacted with BPDE and the adducts derived from binding of BPDE to the exocyclic amino group of deoxyguanosine (dG) were studied with spectroscopic methods. The major dG-adducts of (+)- and (-)-anti-BPDE and a minor adduct of (+)-syn-BPDE showed the characteristics of trans-adducts. The major products formed with (+)- and (-)-syn-BPDE exhibit cis-adduct characteristics. Annealing of BPDE-modified oligonucleotides to complementary or partially complementary strands results in reduced fluorescence intensity in several cases and in others the intensity is markedly increased. These differences demonstrate that the adduct microenvironment is strongly influenc…

Polymers and PlasticsOligonucleotideStereochemistryOrganic ChemistryEpoxyPhotochemistryAdductchemistry.chemical_compoundchemistryDuplex (building)visual_artpolycyclic compoundsMaterials Chemistryvisual_art.visual_art_mediumPyreneDeoxyguanosineThermal stabilityBase sequencePolycyclic Aromatic Compounds
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