Search results for "Molar"

showing 10 items of 1069 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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Preparative fractionation and characterization of polycarbonate/eugenol-siloxane copolymers

2002

Bisphenol-A polycarbonate/eugenol-siloxane copolymers were fractionated at the preparative scale by the continuous polymer fractionation (CPF) technique. It is the first example of copolymer fractionation by CPF. The distribution of siloxane species across the fractions was assessed for copolymers differing in initial siloxane concentration and block length. On- and off-line combinations of size exclusion chromatography and infrared spectroscopy were used to analyze chemical composition (CC) of the unfractionated samples across the molecular weight distribution enabling comparison with the fractions. A polycarbonate-siloxane copolymer containing 10 wt% of very short siloxane blocks (dp = 2)…

Polymers and PlasticsChemistryOrganic ChemistrySize-exclusion chromatographyFractionationDegree of polymerizationchemistry.chemical_compoundChemical engineeringSiloxanevisual_artPolymer chemistryMaterials ChemistryCopolymervisual_art.visual_art_mediumMolar mass distributionPolymer fractionationPolycarbonatePolymer
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Estimation of Number-Average Molecular Weights of Copolymers by Gel Permeation Chromatography−Light Scattering

1996

The true number-average molecular weight, Mn, of copolymers is obtained by GPC coupled with a light-scattering detector even if the composition and therefore the refractive index increment varies with elution volume, provided slices taken are monodisperse with respect to molecular weight and composition. In contrast, only an apparent weight-average molecular weight, can be obtained by the conventional GPC−light scattering combination, even for a perfect chromatographic resolution. The errors in Mn associated with nonhomogeneous slices are estimated. Experimental data with mixtures of linear polystyrene and poly(methyl methacrylate) confirm these estimations and indicate that the error in Mn…

Polymers and PlasticsElutionScatteringOrganic ChemistryDispersityAnalytical chemistryLight scatteringInorganic ChemistryGel permeation chromatographychemistry.chemical_compoundchemistryMaterials ChemistryMolar mass distributionPolystyreneMethyl methacrylateMacromolecules
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ABC triblock polyampholytes containing a neutral hydrophobic block, a polyacid and a polybase

1997

Well defined ABC triblock copolymers of polystyrene-block-poly(2-vinylpyridine)-block-poly(tert-butyl methacrylate) and polystyrene-block-poly(4-vinylpyridine)-block-poly(tert-butyl methacrylate) were synthesized by sequential living anionic polymerization in tetrahydrofuran. Triblock copolymers with narrow molecular weight distribution were obtained. Hydrolysis of the poly(tert-butyl methacrylate) block yields polystyrene-block-polyvinylpyridine-block-poly(methacrylic acid) which demonstrates pH-dependent solution properties. Interpolymer complexation of the polyvinylpyridine and poly(methacrylic acid) blocks in the micellar solution is studied in dependence of the pH in solution by potent…

Polymers and PlasticsOrganic ChemistryPotentiometric titrationCondensed Matter PhysicsMethacrylatechemistry.chemical_compoundchemistryMethacrylic acidPolymer chemistryMaterials ChemistryCopolymerMolar mass distributionTitrationPhysical and Theoretical ChemistryTetrahydrofuranLiving anionic polymerizationMacromolecular Chemistry and Physics
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Role of organo-modifier and metal impurities of commercial nanoclays in the photo-and thermo-oxidation of polyamide 11 nanocomposites

2020

The photo-oxidative degradation processes of bio-based PA11 nanocomposites containing montmorillonite (MMT) and the organo-modified Cloisite&reg

Polymers and PlasticsSize-exclusion chromatographythermo-oxidationMass spectrometryArticleNanocompositeslcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryImpuritypolyamide 11 nanocompositesPhoto-oxidationMontmorillonitechemistry.chemical_classificationNanocompositeNanocompositeMolar massBio polyamideThermooxidationGeneral ChemistryPolymerCloisite® 30BPA11MontmorilloniteSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryChemical engineeringPolyamide
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Calorimetric and Volumetric Investigations of the Effect of the Hydrophobicity of the Surfactant on the Binding between (Ethylene oxide)13-(propylene…

2004

The enthalpy and the volume of transfer (DeltaY(t)) of the unassociated (ethylene oxide)(13)-(propylene oxide)(30)-(ethylene oxide)(13) (L64) from water to the aqueous sodium alkanoate solutions as functions of the surfactant concentrations (m(S)) were determined at 298 K. The surfactants studied are sodium hexanoate, sodium heptanoate, sodium octanoate, sodium undecanoate, and sodium dodecanoate. As a general feature, for the short alkyl chain surfactants, DeltaY(t) describes an S-shaped curve in the range of m(S) analyzed whereas for the more hydrophobic surfactants the DeltaY(t) vs m(S) trends exhibit maxima which appear at ms values very close to the critical micellar concentration in w…

Polymers and PlasticsSodiumInorganic chemistryEnthalpyFLUORINATED ALCOHOLSchemistry.chemical_elementIONIC SURFACTANTSHEAT-CAPACITYTRIBLOCK COPOLYMERSInorganic Chemistrychemistry.chemical_compoundPulmonary surfactantMaterials ChemistryWATERMOLAR VOLUMESCarboxylatePropylene oxideAqueous solutionEthylene oxideOrganic ChemistrySECONDARY ALCOHOLSMICELLAR SOLUTIONSDODECYLTRIMETHYLAMMONIUM BROMIDEchemistryVolume (thermodynamics)THERMODYNAMIC PROPERTIES
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Kinetic analysis of "living" polymerization processes exhibiting slow equilibria. 6. Cationic polymerization involving covalent species, ion pairs, a…

1996

The kinetics of cationic polymerization is studied theoretically in accordance with a three-state mechanism which consists of two successive equilibria:  the ionization/ion collapse equilibrium between covalent species and ion pairs, and the subsequent dissociation/association equilibrium between ion pairs and free ions. The number- and weight-average degrees of polymerization and the polydispersity index (PDI), Pw/Pn, are derived. The molecular weight distribution of the polymer generated from this mechanism is generally broader than that of polymers formed via a two-state mechanism, i.e. with only one equilibrium either between covalent species and ion pairs or between covalent species an…

Polymers and PlasticsStereochemistryChemistryOrganic ChemistryDispersityCationic polymerizationSolution polymerizationPhotochemistryDissociation (chemistry)Inorganic ChemistryPolymerizationCovalent bondMaterials ChemistryMolar mass distributionLiving polymerization
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Suzuki-Miyaura cross-coupling of arenediazonium salts catalyzed by alginate/gellan-stabilized palladium nanoparticles under aerobic conditions in wat…

2012

The use of palladium nanoparticles stabilized by natural. beads made of an alginate/gellan mixture in the Suzuki-Miyaura cross-coupling reaction of arenediazonium. tetrafluoroborates with potassium aryltrifluoroborates. (1 : 1 molar ratio) with loading as low as 0.01–0.002. mol% under aerobic, phosphine-, and base-free conditions. in water is described. The catalyst system can be reused. several times without significant loss of activity.

PotassiumInorganic chemistryalginate palladium nanoparticlesPalladium nanoparticleschemistry.chemical_elementPollutionCatalysischemistry.chemical_compoundchemistryMolar ratioEnvironmental ChemistryCoupling (piping)PhosphineSettore CHIM/02 - Chimica FisicaNuclear chemistry
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The effect of dentine pre-treatment using bioglass and/or polyacrylic acid on the interfacial characteristics of resin-modified glass ionomer cements.

2018

Objective To evaluate the effect of load-cycle aging and/or 6 months artificial saliva (AS) storage on bond durability and interfacial ultramorphology of resin-modified glass ionomer cement (RMGIC) applied to dentine air-abraded using Bioglass 45S5 (BAG) with/without polyacrylic acid (PAA) conditioning.Methods RMGIC (Ionolux, VOCO) was applied onto human dentine specimens prepared with silicon-carbide abrasive paper or air-abraded with BAG with or without the use of PAA conditioning. Half of bonded-teeth were submitted to load cycling (150,000 cycles) and half immersed in deionised water for 24 h. They were cut into matchsticks and submitted immediately to microtensile bond strength (μTBS) …

Pre treatmentAdultCeramicsMaterials scienceSurface PropertiesGlass ionomer cementAcrylic Resins02 engineering and technologylaw.invention03 medical and health scienceschemistry.chemical_compoundTooth FracturesYoung Adult0302 clinical medicinestomatognathic systemlawBioglass 45S5Tensile StrengthLoad cyclingMaterials TestingHumansDental Restoration FailureComposite materialGeneral DentistryDental LeakageBond strengthPolyacrylic acidDental BondingResin modified030206 dentistry021001 nanoscience & nanotechnologyMolarResin CementsAir Abrasion DentalchemistryGlass Ionomer CementsBioactive glassDentin-Bonding AgentsDentinGlass0210 nano-technologyJournal of dentistry
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