Search results for "polymers"

showing 10 items of 3567 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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Calculation of vapor pressures not requiring the derivatives of the energy of mixing

1997

A method is presented for the calculation of vapor pressures exclusively on the basis of the energy of mixing, the knowledge of chemical potentials is not required. The only condition used for the calculation is the minimum of the energy of mixing of the overall system in equilibrium. The gas phase is treated as an ideal gas, for the liquid phase no specific thermodynamic description is assumed. The method is demonstrated for a mixture of two solvents and one polymer. The system water/poly(ethylene oxide), the thermodynamics of which are described by an equation that can only be solved numerically thus impeding the calculation of chemical potentials, serves as an example. Interaction parame…

chemistry.chemical_classificationPolymers and PlasticsBasis (linear algebra)Ethylene oxideOrganic ChemistryLiquid phaseThermodynamicsPolymerCondensed Matter PhysicsIdeal gasGas phaseInorganic Chemistrychemistry.chemical_compoundchemistryMaterials ChemistryMixing (physics)Energy (signal processing)Macromolecular Theory and Simulations
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Water-soluble hyperbranched polyglycerol photosensitizer for enhanced photodynamic therapy

2020

Porphyrin and its derivatives as promising photosensitizers have been widely utilized in photodynamic therapy (PDT). However, the water-solubility and biocompatibility of porphyrins are the typical bottlenecks in clinical PDT processes. Herein, we successfully fabricated a new type of water-soluble, hyperbranched polyglycerol photosensitizer through one-step esterification between water-soluble hyperbranched polyglycerol (hbPG) and fluorophenylporphyrin (FP). Compared with the linear control polymer, i.e., FP covalently connected with linear polyethylene glycol (LPEG), the hyperbranched structures bearing multiple porphyrin units generated more singlet oxygen and exhibited higher cytotoxici…

chemistry.chemical_classificationPolymers and PlasticsBiocompatibilitySinglet oxygenmedicine.medical_treatmentOrganic ChemistryBioengineeringPhotodynamic therapyPolymerBiochemistryCombinatorial chemistryPorphyrinchemistry.chemical_compoundchemistryCovalent bondpolycyclic compoundsmedicinePhotosensitizerCytotoxicityPolymer Chemistry
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Patterning of a Surface Immobilized ATRP Initiator with an Inkjet Printer

2010

A new technique for patterning polymer brushes on the micrometer scale has been developed in which an inkjet printer was used to deposit droplets of acid on a surface-immobilized initiator for atom transfer radical polymerization (ATRP). The acid cleaved an ester bond in the ATRP initiator in a saponification reaction. As a result, the ATRP initiator was rendered inactive. To control the degree of defunctionalization, a new initiator containing a weak ester bond was derived from a tertiary alcohol. Comparison to an established ATRP initiator, derived from a primary alcohol, showed that the novel initiator was defunctionalized with a higher efficiency. Control of the reaction time allowed to…

chemistry.chemical_classificationPolymers and PlasticsBulk polymerizationChemistryAtom-transfer radical-polymerizationOrganic ChemistryAlcoholPolymerPrimary alcoholGraftingInorganic Chemistrychemistry.chemical_compoundPolymer chemistryMaterials ChemistryMoleculeSaponificationMacromolecules
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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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Oligoethyleneoxide spacer groups in polymerizable surfactants

1991

Cationic and zwitterionic polymerizable surfactants bearing tri- and tetraethyleneglycol spacer groups between the polymerizable moiety and the surfactant structure were prepared and polymerized. Monomers and polymers were investigated with respect to their aggregation behavior in aqueous systems and compared to analogous monomers and polymers lacking spacer groups. In the case of the monomeric surfactants, the spacer groups depress both the Kraffttemperature and the critical micelle concentration. the area occupied per molecule at the air-water interface is substantially enlarged by the spacers, whereas the depression of surface tension is nearly constant. Although the monomers with and wi…

chemistry.chemical_classificationPolymers and PlasticsCationic polymerizationPolymerMicelleKrafft temperaturechemistry.chemical_compoundColloid and Surface ChemistryMonomerPulmonary surfactantchemistryCritical micelle concentrationddc:540Polymer chemistryMaterials ChemistryInstitut für ChemieMoietyPhysical and Theoretical ChemistryColloid & Polymer Science
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Melt stabilization of wet polyamide 6

2002

Abstract Melt processing of polycondensate polymers must be carried out after careful drying in order to avoid any hydrolytic chain scission caused by the presence of water or other small molecules. In this work, the effect of two different antioxidants on the processing and flow properties of a polyamide 6 sample not dried before processing operations has been studied. One of these stabilizers seems to protect the wet polymer from hydrolytic chain scission. This action has been interpreted considering that the stabilizer hydrolyses instead of the polyamide macromolecules.

chemistry.chemical_classificationPolymers and PlasticsChain scissionPolymerCondensed Matter PhysicsHydrolysisMolten stateSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryMechanics of MaterialsPolyamidePolymer chemistryMaterials ChemistryFlow propertiesmelt stabilization polyamide recycling processing stabilizationMacromoleculeStabilizer (chemistry)
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Poly-l-Lysine-Poly[HPMA] Block Copolymers Obtained by RAFT Polymerization as Polyplex-Transfection Reagents with Minimal Toxicity

2015

Herein we describe the synthesis of poly-L-lysine-b-poly[N-(2-hydroxypropyl)-metha-crylamide)] (poly[HPMA]) block copolymers by combination of solid phase peptide synthesis or polymerization of α-amino acid-N-carboxy-anhydrides (NCA-polymerization) with the reversible addition-fragmentation chain transfer polymerization (RAFT). In the presence of p-DNA, these polymers form polyplex micelles with a size of 100-200 nm in diameter (monitored by SDS-PAGE and FCS). Primary in vitro studies with HEK-293T cells reveal their cellular uptake (FACS studies and CLSM) and proof successful transfection with efficiencies depending on the length of polylysine. Moreover, these polyplexes display minimal to…

chemistry.chemical_classificationPolymers and PlasticsChemistryBioengineeringChain transferPolymerRaftMicelleBiomaterialschemistry.chemical_compoundPolymerizationPolylysinePolymer chemistryMaterials ChemistryCopolymerBiophysicsReversible addition−fragmentation chain-transfer polymerizationBiotechnologyMacromolecular Bioscience
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Homogeneous mixtures of polybetaines with low molecular weight salts

1996

The prepaparation of amorphous, homogeneous blends of zwitterionic polymers with various low molecular weight salts, and in particular with ionic dyes was studied. Homogeneous miscibility was achieved in many cases up to equimolar amounts of salt, even for bulky compounds. Whether miscibility is achieved, or not, depends in a subtle way on the chemical structure of the salt, but no obvious correlation between structure and miscibility could yet be revealed. Spectral shifts of the dye UV/Vis spectra in solution as well as in bulk suggest strong interactions between the polybetaines and the admired salts.

chemistry.chemical_classificationPolymers and PlasticsChemistryChemical structureOrganic ChemistryInorganic chemistrySalt (chemistry)Ionic bondingVis spectraPolymerCondensed Matter PhysicsMiscibilityAmorphous solidHomogeneousMaterials ChemistryMacromolecular Symposia
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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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