Search results for "Molar"

showing 10 items of 1069 documents

Viscometry of polyelectrolyte solutions: Star-like versus linear poly[[2-(methacryloyloxy)ethyl] trimethylammonium iodide] and specific salt effects

2017

Abstract The intrinsic viscosities, [η], of the 3-arm star polyelectrolyte in pure water are for a given molar mass considerably lower than for the linear product because of the higher monomer concentration and charge density in isolated coils. These effects are much more pronounced than in the case of uncharged macromolecules. Extra salt (NaCl, NaI, CaCl2) reduces the solution viscosities of the 3-arm star polymer less than of the linear product. The transition of [η] from the value in pure water to the minimum saturation value at high salt concentrations follows a Boltzmann sigmoid. In saline solvents the changes of the viscosities with rising polymer concentration depend strongly on the …

chemistry.chemical_classificationMolar massPolymers and PlasticsOrganic ChemistryIodideGeneral Physics and AstronomyThermodynamicsViscometerSalt (chemistry)Charge density02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesPolyelectrolyte0104 chemical scienceschemistry.chemical_compoundMonomerchemistryMaterials ChemistryOrganic chemistry0210 nano-technologyEuropean Polymer Journal
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Polymer-polymer interaction, in the presence of a solvent as measured by viscometry

2001

Dilute solution viscometry experiments have been carried out in five ternary polymer systems solvent(1)/polymer(2)/polymer(3). Values of the specific viscosity of polymer (3) in a ‘binary solvent’ formed by polymer(2) + solvent(1) have been used to determine the compatibility of the polymer blends. Krigbaum and Wall formalism has been used to predict compatibility which relies on an interaction parameter that depends on the concentration, weight fraction and molar mass of each polymer. To reduce the dependences and to clarify the criterion of compatibility, a parameter independent of polymer (3) composition and molar mass has been deduced. This parameter shows the same behaviour with polyme…

chemistry.chemical_classificationMolar massTernary numeral systemPolymers and PlasticsIntrinsic viscosityOrganic ChemistryThermodynamicsViscometerPolymerFlory–Huggins solution theorychemistryPolymer chemistryMaterials ChemistryMolar mass distributionPolymer blendPolymer International
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Dithienopyrrolobenzotriazole-based organic dyes with high molar extinction coefficient for efficient dye-sensitized solar cells

2016

Abstract Four novel organic dyes DT1-DT4 containing a dithienopyrrolobenzotriazole unit were synthesized and applied in dye sensitized solar cells, where dithienopyrrolobenzotriazole moiety was introduced as a π-spacer for the first time. The four dyes exhibited good light harvesting efficiency with high molar extinction coefficients and broad spectral response. The influence of the different electron donor on the photovoltaic performance was evaluated. The effects of the linear and branched alkyl chains in the π-bridge on the photophysical, electrochemical and photovoltaic performance were systemically investigated. The results show that branched alkyl chains are better than linear alkyl c…

chemistry.chemical_classificationOrganic solar cellProcess Chemistry and TechnologyGeneral Chemical EngineeringElectron donor02 engineering and technologyHybrid solar cellMolar absorptivity010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciences0104 chemical scienceslaw.inventionchemistry.chemical_compoundDye-sensitized solar cellchemistrylawSolar cellMoiety0210 nano-technologyAlkylDyes and Pigments
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The Efficiency of Polymer Fractionation at Lower Critical Solution Temperatures

1978

The efficiency of a single fractionation step (i.e. of the partition of a given polymer sample between the coexisting phases which form when its solution demixes) is governed by the variation of the mass ratio of the individual P-mers with chain length. These dependences have been measured for the system dimethoxymethane/diethylether/ polystyrene which exhibits lower critical solution temperatures by means of the Baker-Williams method and by means of g.p.c. Their comparison with the results of previous investigation on systems showing upper critical solution temperatures reveals no thermodynamic differences in the aptitude of upper and lower critical solution temperatures for fractionation …

chemistry.chemical_classificationPartition coefficientchemistryUpper critical solution temperaturePhase (matter)General EngineeringMolar mass distributionThermodynamicsGeneral Materials ScienceFractionationPolymerPolymer fractionationLower critical solution temperatureBritish Polymer Journal
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Shear induced mixing/demixing: blends of homopolymers, of homopolymers plus copolymers, and blends in solution

2000

Shear may shift the phase boundary towards the homogeneous state (shear induced mixing, SIM), or in the opposite direction (shear induced demixing, SID). SIM is the typical behavior of mixtures of components of low molar mass and polymer solutions, SID can be observed with solutions of high molar mass polymers and polymer blends at higher shear rates. The typical sequence with increasing shear rate is SIM, then occurrence of an isolated additional immiscible area (SLD), melting of this island into the main miscibility gap, and finally SIM again. A three phase line originates and ends in two critical end points. Raising pressure increases the shear effects. For copolymer containing systems S…

chemistry.chemical_classificationPhase boundaryMolar massMaterials sciencePolymers and PlasticsSpinodal decompositionOrganic ChemistryThermodynamicsPolymerCondensed Matter PhysicsShear ratechemistryShear (geology)Materials ChemistryCopolymerOrganic chemistryPolymer blendMacromolecular Symposia
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Novel dithieno[3,2-b:2′,3′-d]pyrrole-based organic dyes with high molar extinction coefficient for dye-sensitized solar cells

2013

Abstract Three new metal-free organic dyes FD1 – 3 with a planar dithieno[3,2- b :2′,3′- d ]pyrrole unit as linker were synthesized and used for dye-sensitized solar cells with high molar extinction coefficients. In this work, dithieno[3,2- b :2′,3′- d ]pyrrole was employed as π-conjugated bridge to construct A–π– d –π–A organic dyes, where 9,9-dihexyl-9 H -fluorene was used as a donor, and cyanoacrylic acid as an electron acceptor. For a typical device, a solar energy conversion efficiency ( η ) of 6.36% based on FD2 was achieved under simulated AM 1.5 solar irradiation (100 mW cm −2 ) with a short-circuit photocurrent density ( J sc ) of 13.76 mA cm −2 , an open-circuit voltage ( V oc ) o…

chemistry.chemical_classificationPhotocurrentMaterials scienceGeneral ChemistryElectron acceptorMolar absorptivityFluoreneCondensed Matter PhysicsPhotochemistryElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundDye-sensitized solar cellchemistryExtinction (optical mineralogy)Materials ChemistryIrradiationElectrical and Electronic EngineeringPyrroleOrganic Electronics
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Innovative Combination of Three Alternating Current Relaxation Techniques: Electrical Charge, Mass, and Color Impedance Spectroscopy. Part I: The Tool

2009

Technical details concerning the simultaneous acquisition of three impedance functions (electrochemical impedance spectroscopy, alternating current electrogravimetry or mass impedance, and alternating current colorimetry or color impedance) are presented. The analysis of each type of impedance function gives interesting information about the species participating during the electrochemical processes. Furthermore, obtaining three impedance functions in situ allows the crossed impedance functions to be calculated. These functions are especially useful in detecting delays between the color, mass, and electrical charge response of the system to the same perturbation, and it allows species parti…

chemistry.chemical_classificationPhysical modelMolar massChemistryAnalytical chemistryPolymerElectric chargeSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsComputational physicslaw.inventionDielectric spectroscopyGeneral EnergylawElectrogravimetryPhysical and Theoretical ChemistryAlternating currentElectrical impedanceThe Journal of Physical Chemistry C
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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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Molecular Weight Distribution of Hyperbranched Polymers Generated by Self-Condensing Vinyl Polymerization in Presence of a Multifunctional Initiator

1999

The molecular weight distribution (MWD) is derived for polymers generated by self-condensing vinyl polymerization (SCVP) of a monomer having a vinyl and an initiator group (“inimer”) in the presence of a multifunctional initiator. If the monomer is added slowly to the initiator solution (semi-batch process), this leads to hyperbranched polymers with a multifunctional core. If monomer and initiator are mixed simultaneously (batch process), even at vinyl group conversions as high as 99%, the total MWD consists of polymers which have grown via reactions between inimer molecules (i.e., the normal SCVP process) and those which have reacted with the initiator. Consequently, the weight distributio…

chemistry.chemical_classificationPolymers and PlasticsBulk polymerizationOrganic ChemistryPolymerSelf-condensationInorganic Chemistrychemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistryWeight distributionMaterials ChemistryMolar mass distributionMoleculeMacromolecules
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Influence of Molar Mass Distribution on the Compatibility of Polymers

1996

Abstract Phase equilibria were calculated by means of a new method (direct minimization of the Gibbs energy of mixing) for polymer blends consisting of monodisperse polymer A and polydisperse polymer B. The results obtained for a Schulz-Flory distribution of B (molecular nonuniformity U = (M w/M n) −1 = 1 and 100 components of model B) agree quantitatively with that of computations on the basis of continuous thermodynamics. The influence of U B on the miscibility of A and B in 1:1 mixtures was studied for constant M w of B, quantifying the incompatibility of the polymers by the length of the tie lines. The outcome of these calculations demonstrates that the typical effect of an augmentation…

chemistry.chemical_classificationPolymers and PlasticsDispersityThermodynamicsGeneral ChemistryPolymerMiscibilityGibbs free energysymbols.namesakechemistryMaterials ChemistryCeramics and CompositessymbolsMolar mass distributionBinary systemPolymer blendPhase diagramJournal of Macromolecular Science, Part A
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