Search results for "surface"

showing 10 items of 9345 documents

1991

The polysoaps [CH 2 C(Me)(CO 2 R)] n (R=(CH 2 ) 11 N + Me 2 (CH 2 ) 3 SO 3 − , (CH 2 ) 11 N + Me 2 CH 2 CH 2 OH) are studied. Their aqueous solution properties are strongly influenced by added salts; the surface activity can be modified efficiently by an appropriate choice of ions. The interactions of salts and polyzwitterions observed in solution can be extended to the behaviour in bulk. It enables the preparation of uniform, non crystalline blends containing up to equivalent amounts of inorganic salt and polyzwitterions

chemistry.chemical_classificationSurface tensionInorganic saltsAqueous solutionchemistryPolymer chemistryCationic polymerizationSalt (chemistry)Concentration effectPolyelectrolyteIonDie Makromolekulare Chemie, Rapid Communications
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Reduction of the frequency of herbaceous roots as an effect of soil compaction induced by heavy grazing in rangelands of SW Spain

2017

Rangelands in SW Spain constitute the most extensive ranching system on the Iberian Peninsula. During the last few decades, a significant increase in livestock numbers, along with a progressive substitution of cattle for sheep, have led to land degradation processes such as the reduction of grass cover and increased soil compaction in heavily grazed areas. Nevertheless, a better understanding of how soil compaction affects grass production is still needed. In this study, some of the effects of soil compaction due to heavy grazing are analysed, mainly the reduction of the frequency of herbaceous roots and its relationships with bulk density and soil penetration resistance. The study was carr…

chemistry.chemical_classificationSòls ErosióSoil organic matterSoil science04 agricultural and veterinary sciences010501 environmental sciencesHerbaceous plant01 natural sciencesBulk densitychemistryAgronomyGrazing040103 agronomy & agriculture0401 agriculture forestry and fisheriesSoil horizonEnvironmental scienceOrganic matterRangelandWater content0105 earth and related environmental sciencesEarth-Surface ProcessesCATENA
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Heterotelechelic Ring-Opening Metathesis Polymers

2009

By combining sacrificial synthesis with the vinyl lactone termination technique, heterotelechelic polymers were synthesized. The nonterminating nature of sacrificial synthesis was utilized to introduce a hydroxyl group at the start of the polymer chain. Lactone termination was used to functionalize the chain ends with aldehydes or carboxylic acids. The synthesis of well-defined heterotelechelic polymers was thus accomplished employing the Grubbs’ first generation catalyst as the initiator. The living nature of this polymerization allowed for precise control over the molecular weight and guaranteed full functionalization of both polymer chain ends. The presence of the functional groups is sh…

chemistry.chemical_classificationTelechelic polymerPolymers and PlasticsChemistryOrganic ChemistryPolymerRing (chemistry)MetathesisInorganic Chemistrychemistry.chemical_compoundPolymerizationPolymer chemistryMaterials ChemistrySurface modificationImideLactoneMacromolecules
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Sacrificial Synthesis of Hydroxy-Telechelic Metathesis Polymers via Multiblock-Copolymers

2009

The synthesis of well-defined telechelic ring-opening metathesis polymers has been achieved by Sacrificial Synthesis. With the formation of cleavable triblock-copolymers, precise control over the molecular weight and the degree of functionalization was achieved. Introducing cleavable monomers that can be addressed separately, sequential deprotection was accomplished which opened the path to more sophisticated polymeric materials bearing different substituents at their respective chain ends. Sacrificial penta- and heptablock-copolymers are also presented which allow the synthesis of well-defined telechelic polymers in good yields and significantly improved initiator efficiency.

chemistry.chemical_classificationTelechelic polymerPolymers and PlasticsOrganic ChemistryMultiblock copolymerPolymerMetathesisInorganic Chemistrychemistry.chemical_compoundMonomerchemistryPolymer chemistryMaterials ChemistrySurface modificationAcetal copolymerImideMacromolecules
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Interfacial tension of demixed polymer solutions: augmentation by polymer additives

1997

The interfacial tension between phase separated polymer solutions increases pronouncedly upon the addition of asmall amounts of incompatible polymers. This feature is demonstrated by means of measurements with solutions of polystyrene in cyclohexane and the folloowing additives: poly(styrene-block-dimethylsiloxane), polyisobutylene and polydimethylsiloxane. Theoretical considerations based on a correlation between the lenth of the tie lines and the corresponding interfacial tension corroborates this finding

chemistry.chemical_classificationTernary numeral systemMaterials sciencePolymers and PlasticsCyclohexanePolydimethylsiloxaneOrganic ChemistryPolymerSurface tensionchemistry.chemical_compoundchemistryChemical engineeringPhase (matter)Polymer chemistryMaterials ChemistryCopolymerPolystyreneMacromolecular Rapid Communications
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Viscometric behaviour of polymer blends based on poly (vinylidene fluoride)

1994

The viscosity behaviour of dilute dimethylformamide solutions of poly(vinylidene fluoride)-poly (methyl methacrylate) and poly(vinylidene fluoride)-polystyrene has been studied at 25°C. The polymer concentration ranges are such that neither phase separation nor microgel formation occurs, although we are very close to theta conditions. The intrinsic viscosity and viscosity interaction parameter of the ternary mixtures have been calculated. The estimation of the compatibility of the above polymer pairs has been studied based on: a) specific viscosities; b) viscosity interaction parameters, according to Krigbaum and Wall formalism, and c) viscosity interaction parameters of a system formed by …

chemistry.chemical_classificationTernary numeral systemMaterials sciencePolymers and PlasticsIntrinsic viscosityRelative viscosityPolymerFlory–Huggins solution theoryPhysics::Fluid DynamicsCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundColloid and Surface ChemistrychemistryChemical engineeringPolymer chemistryMaterials ChemistryPolymer blendPhysics::Chemical PhysicsPhysical and Theoretical ChemistryMethyl methacrylateFluorideColloid & Polymer Science
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Correlation between transport and equilibrium properties through the ternary interaction parameter for cosolvent and cononsolvent polymeric systems

1992

A study of the ternary polymer systems dimethyl formamide-ethyl acetate-polystyrene, chloroform-1,4 dioxane-polystyrene and tetrahydrofuran-chloroform-polystyrene was carried out by viscosity and light scattering at 298 K. A good correlation has been found between the excess intrinsic viscosity, unperturbed polymer dimensions, second virial coefficient and the excess Gibbs free energy by using a ternary interaction parameter, dependent on molecular weight. This modification enables the conversion between transport and equilibrium properties.

chemistry.chemical_classificationTernary numeral systemPolymers and PlasticsChemistryIntrinsic viscosityThermodynamicsPolymerFlory–Huggins solution theoryGibbs free energyViscositysymbols.namesakeColloid and Surface ChemistryVirial coefficientMaterials ChemistrysymbolsPhysical and Theoretical ChemistryTernary operationColloid & Polymer Science
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Interfacial tension between coexisting polymer solutions in mixed solvents and its correlation with bulk thermodynamics: phase equilibria (liquid/gas…

2002

Abstract Vapor pressures, phase equilibria and interfacial tensions σ were measured for solutions of poly(dimethylsiloxane) (PDMS, M w [equals]75 kg/mol and M n [equals]50 kg/mol) in mixed solvents of toluene (TL) and ethanol (EtOH) at 30, 40, 50 and 60 °C. The experimental ternary phase diagrams can be modeled quantitatively from the determined concentration and temperature dependent binary interaction parameters χ ij if the experimentally inaccessible composition dependence of χ EtOH/PDMS is adjusted. The relations between σ and the equation of state of the system differ from that applying to single solvents. The exponents as well as the amplitude prefactors of the corresponding scaling l…

chemistry.chemical_classificationTernary numeral systemPolymers and PlasticsChemistryLiquid gasOrganic ChemistryThermodynamicsPolymerTolueneSurface tensionchemistry.chemical_compoundAmplitudeCritical point (thermodynamics)Materials ChemistryPhase diagramPolymer
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Enantioselective self-assembly of antiferromagnetic hexacopper(ii) wheels with chiral amino acid oxamates

2013

The Cu(2+)-mediated self-assembly of oxamato-based ligands derived from either the (S)- or (R)-enantiomers of the amino acid valine leads to the formation of two antiferromagnetically coupled homochiral anionic hexacopper(II) wheels in the presence of templating tetramethylammonium countercations.

chemistry.chemical_classificationTetramethylammoniumStereochemistryMagnetic PhenomenaMetals and AlloysEnantioselective synthesisStereoisomerismValineGeneral ChemistryLigandsCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAmino acidchemistry.chemical_compoundchemistryCoordination ComplexesValineMaterials ChemistryCeramics and CompositesAntiferromagnetismSelf-assemblyCopperChemical Communications
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Fundamental and practical aspects concerning the characterization of smart textiles

2017

The research aims towards a novel methodology of ZnO impregnation onto polyamide supports, in order to attain a special inorganic-organic hybrid polymer material, with increased UV-barrier attributes and high hydrophobicity. The experimental approach employed ZnO micro particles powder. Solutions with different concentrations of ZnO powder dispersed in methanol are prepared as anti-UV finishing agent and applied onto polyamide fabric. The responsive behaviour of this complex polymer network to UV irradiation, the photo protective performance and its time stability, also the hydrophobic character are assessed by different characterization techniques. The proposed method has advantages, like:…

chemistry.chemical_classificationTextileMaterials sciencePolymer networkMicro particlesbusiness.industryProduction costNanotechnologyPolymerchemistrylcsh:TA1-2040Homogeneity (physics)PolyamideSurface chargelcsh:Engineering (General). Civil engineering (General)businessMATEC Web of Conferences
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