Search results for "polymer chemistry"

showing 10 items of 3410 documents

The photochemical rearrangement of polymeric N-(1-pyridinio) amidates. A novel, aqueous photoresist system

1988

Aqueous solutionChemistryPolymer chemistryRadical polymerizationGeneral EngineeringGeneral Materials ScienceChromophorePhotoresistPhotochemistryJournal of Polymer Science: Polymer Letters Edition
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Continuous fractionation of poly[(dimethylimino)decamethylene bromide] and molecular weight dependence of the glass transition

1995

30 g of the ionene poly[(dimethylimino)decamethylene bromide] were fractionated by a continuous counter-current extraction method (CPF) using ethylene glycol monoethyl ether as the solvent and diisopropyl ether as the non-solvent component. The efficiency of the separation was checked by viscometry and gel-permeation chromatography (GPC) measurements. Eight fractions of different molar mass were prepared for differential scanning calorimetry (DSC) experiments. With bromide as counter-ion, the glass transition temperature of the ionene increases from ca. 60 to 85°C as the intrinsic viscosity of this material (in 0,4 M aqueous solutions of KBr at 25°C) rises from ca. 14 to 22 mL/g. When bromi…

Aqueous solutionChromatographyMolar massPolymers and PlasticsIntrinsic viscosityOrganic ChemistryCondensed Matter PhysicsSolventchemistry.chemical_compoundDifferential scanning calorimetrychemistryBromidePolymer chemistryMaterials ChemistryDiisopropyl etherPhysical and Theoretical ChemistryGlass transitionNuclear chemistryMacromolecular Chemistry and Physics
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Shear Induced Demixing and Rheological Behavior of Aqueous Solutions of Poly(N-isopropylacrylamide)

2003

The interrelation between the phase separation behavior and the rheological performance of aqueous solutions of high molecular weight (M w = 1 600 kg/mol) poly(N-isopropylacrylamide) was investigated. The system demixes upon heating and the cloud point temperature, T cp decreases steadily with rising polymer concentration up to 10 wt.-%. The application of shear supports phase separation and reduces T cp markedly. This observation is interpreted in terms of destruction of intersegmental clusters formed in the quiescent state owing to favorable interactions. Intrinsic viscosities and Huggins coefficients as well as the viscosities, η at higher polymer concentrations are closely connected wit…

Aqueous solutionChromatographyPolymers and PlasticsChemistryOrganic ChemistryThermodynamicsConcentration effectCondensed Matter PhysicsLower critical solution temperatureShear ratechemistry.chemical_compoundPolymer chemistryMaterials ChemistryPoly(N-isopropylacrylamide)Physical and Theoretical ChemistryShear flowOrder of magnitudePhase diagramMacromolecular Chemistry and Physics
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Synthesis of Water-Soluble Copolymers Carrying Long-Chain (C12 to C30 ) Aliphatic Moieties

2011

Water-soluble copolymers from mono-1-alkyl itaconates and N-vinyl-2-pyrrolidone are synthesized and characterized. Themono-1-alkyl itaconates are prepared from itaconic anhydride and the related alcohol: 1-dodecanol, 1-octadecanol, 1-docosanol, and 1-triacontanol. The mono-1-triacontyl itaconate is synthesized fromplant growth regulator policosanols extracted from Agave fourcrouydes, where 1-triacontanol is the major product. The reactivity ratios, calculated according to the Mao-Huglin method for copolymerizations conducted to medium-high conversions, indicate a tendency toward alternation for all copolymerization reactions. Water solubility of copolymers is provided as a function of copol…

Aqueous solutionCopolymer compositionPolymers and PlasticsChemistryOrganic ChemistryRadical polymerizationAlcoholCondensed Matter PhysicsChain lengthchemistry.chemical_compoundWater solublePolymer chemistryMaterials ChemistryCopolymerOrganic chemistryPhysical and Theoretical ChemistryLong chainMacromolecular Chemistry and Physics
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A thermodynamic study to evidence the alpha,omega-dichloroalkane/ block copolymer mixed aggregates formation: effect of the copolymer architecture.

2006

Abstract The thermodynamics of α , ω -dichloroalkanes in aqueous solutions of (ethylene oxide)11(propylene oxide)16(ethylene oxide)11 (L35) and (propylene oxide)8(ethylene oxide)23(propylene oxide)8 (10R5) was determined at 298 and 305 K. Modeling the experimental data allowed to calculate the standard free energy ( Δ G D o / w ) and the volume ( Δ V D / w ) for the additive–copolymer mixed aggregates formation per additive molecule. Δ G D o / w for Cl2CH2 and Cl2(CH2)2 evidenced that the process is controlled by the forces exercising between the chlorine atoms and the OH groups of the copolymer micelles protruded into the aqueous phase. Cl2(CH2)3 experiences both the hydrophilic and hydrop…

Aqueous solutionEthylene oxideEthylene oxide)11(propylene oxide)16(ethylene oxide)11TemperatureAqueous two-phase systemMicelleSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGibbs free energyBiomaterialsHydrophobic effectsymbols.namesakechemistry.chemical_compoundColloid and Surface Chemistrychemistry(Propylene oxide)8(ethylene oxide)23(propylene oxide)8-DichloroalkanePolymer chemistryCopolymersymbolsStandard free energyPhysical chemistryPropylene oxideJournal of colloid and interface science
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Aqueous nonionic copolymer-functionalized laponite clay. A thermodynamic and spectrophotometric study to characterize its behavior toward an organic …

2006

The affinity of functionalized Laponite clay toward an organic material in the aqueous phase was explored. Functionalization was performed by using triblock copolymers based on ethylene oxide (EO) and propylene oxide (PO) units that are EO(11)PO(16)EO(11) (L35) and PO(8)EO(23)PO(8) (10R5). Phenol (PhOH) was chosen as organic compound, which represents a contaminant prototype. To this purpose, densities and enthalpies of mixing as well as PhOH UV-absorption spectra were determined. The enthalpy and the spectrophotometry revealed PhOH-Laponite interactions whereas the volume did not. It emerged that the area occupied by PhOH on the Laponite surface is equal to that computed from the partial m…

Aqueous solutionEthylene oxideSuspensions (fluids)Aqueous two-phase systemPartial molar propertySurfaces and InterfacesCondensed Matter Physicsyield stresschemistry.chemical_compoundAdsorptionchemistryChemical engineeringPolymer chemistryBentoniteElectrochemistryCopolymerSurface modificationGeneral Materials SciencePropylene oxideSpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Aqueous block copolymer-surfactant mixtures and their ability in solubilizing chlorinated organic compounds. A thermodynamic and SANS study.

2006

Within the topic of surfactant enhanced solubilization of additives sparingly soluble in water, volumetric, solubility, conductivity, and small-angle neutron scattering (SANS) experiments on mixtures composed of alpha,omega-dichloroalkane, surfactant, copolymer, and water were carried out at 298 K. The triblock copolymers (ethylene oxide)132(propylene oxide)50(ethylene oxide)132 (F108) and (ethylene oxide)76(propylene oxide)29(ethylene oxide)76 (F68) were chosen to investigate the role of the molecular weight keeping constant the hydrophilic/hydrophobic ratio. The selected surfactants are sodium decanoate (NaDec) and decyltrimethylammonium bromide (DeTAB) with comparable hydrophobicity and …

Aqueous solutionEthylene oxidescattering DLSConductivitySurfaces Coatings and Films| Micelleschemistry.chemical_compoundMonomerchemistryPulmonary surfactantChemical engineeringPolymer chemistryMaterials ChemistryCopolymerPropylene oxidePolyethylene oxidePhysical and Theoretical ChemistrySolubilityThe journal of physical chemistry. B
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Solubilization of an Organic Solute in Aqueous Solutions of Unimeric Block Copolymers and Their Mixtures with Monomeric Surfactant: Volume, Surface T…

2008

The ability of aqueous systems, formed by unimeric copolymers and their mixtures with a monomeric surfactant, in solubilizing large quantities of 1-nitropropane (PrNO2) was explored. The copolymers are F68 and L64, which differ for the hydrophilicity, and the surfactant is sodium dodecanoate. For a better understanding of the mechanism of solubilization, thermodynamic (volume and differential scanning calorimetry), spectroscopy (steady-state fluorescence), viscosity, and interfacial investigations were carried out. PrNO2 causes the micellization of the unimeric copolymer, and the required amount of PrNO2 depends on the composition, the copolymer nature, and the temperature. Large quantities…

Aqueous solutionISOTHERMAL TITRATION CALORIMETRYChemistryMICELLAR SYSTEMSDYNAMIC LIGHT-SCATTERINGIONIC SURFACTANTSTRIBLOCK COPOLYMERSMicelleFluorescence spectroscopySurfaces Coatings and FilmsSurface tensionViscosityDifferential scanning calorimetryAGGREGATION BEHAVIORPulmonary surfactantChemical engineeringMIXED MICELLESPolymer chemistryMaterials ChemistryCopolymerPhysical and Theoretical ChemistrySODIUM DODECYL-SULFATEOXIDE)(13)-(PROPYLENE OXIDE)(30)-(ETHYLENE OXIDE)(13)GEMINI SURFACTANTS
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Dendritic octa-CMPO derivatives of calix[4]arenes

2004

Abstract Calix[4]arenes substituted at the narrow or wide rim by eight carbamoylmethyl-phosphine oxide (CMPO) functions in a dendritic manner were synthesised and studied in extraction of Eu 3+ and Am 3+ from aqueous nitric acid into o -nitrophenylhexyl ether. 1 H NMR relaxivity titrations for a wide rim octa-CMPO reveal the clear formation of a solvent-free 1:2 ligand/metal complex, while the wide rim tetra-CMPO formed oligomeric complexes under similar conditions.

Aqueous solutionLigandOrganic ChemistryInorganic chemistryEtherBiochemistryMetalchemistry.chemical_compoundchemistryNitric acidDendrimervisual_artDrug DiscoveryPolymer chemistryProton NMRvisual_art.visual_art_mediumTitrationTetrahedron
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Electrochemistry of copper complexes with macrocyclic polyamines containing pyrazole units.

2006

The voltammetric behaviour of bi- and mono-nuclear complexes formed in solution by Cu(2+) with three polyazacyclophanes containing pyrazole units in aqueous solution is described. Cyclic and square wave voltammetric responses at glassy carbon electrodes indicate that the reduction of copper-macrocycle complexes in solution takes place in two successive one-electron per Cu transfer processes coupled with preorganization and protonation reactions that mimic the behaviour of superoxide dismutase. The electrochemistry of ternary Cu(2+)-receptor-dopamine complexes exhibits significant differences with respect to the protection of the neurotransmitter from post-electron transfer cyclization react…

Aqueous solutionMacrocyclic CompoundsSuperoxide DismutaseDopamineInorganic chemistryMolecular Mimicrychemistry.chemical_elementProtonationSquare wavePyrazoleGlassy carbonElectrochemistryCopperInorganic Chemistrychemistry.chemical_compoundchemistryPolymer chemistryElectrochemistryOrganometallic CompoundsPolyaminesPyrazolesTernary operationCopperDalton transactions (Cambridge, England : 2003)
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