Search results for " Coating."

showing 10 items of 2558 documents

A general concept for the introduction of hydroxamic acids into polymers.

2019

Polyethers (PEG) with hydroxamic acid groups enable chelation of a variety of metal ions, coating of metal oxide surfaces and stabilization of nanoparticles. In contrast to catechol, hydroxamic acids are oxidation stable and biocompatible.

chemistry.chemical_classificationHydroxamic acidEthylene oxide010405 organic chemistryGeneral ChemistryPolymer010402 general chemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundSurface coatingChemistryMonomerPolypropylene glycolchemistryOrganic chemistryFunctional polymersEthylene glycolChemical science
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Evaporation of tungsten oxides: A mass-spectrometric study of the vapour contents

1995

Abstract The evaporation of bulk oxides of WO2 and WO3 and oxidised tungsten surfaces (metallic tungsten heated in an oxygen atmosphere) have been studied by the means of mass-spectrometry. The principal constituents of the vapour are found to be molecules of WO2, WO3, W2O6 and W3O9. These results differ from earlier reports, where the presence of molecules smaller than W3O9 in the mass-spectrum was interpreted as an artifact due to electron impact dissociation of larger polymers.

chemistry.chemical_classificationInorganic chemistryAnalytical chemistrychemistry.chemical_elementPolymerTungstenequipment and suppliesCondensed Matter PhysicsMass spectrometryDissociation (chemistry)Surfaces Coatings and FilmsMetalchemistryvisual_artMass spectrumvisual_art.visual_art_mediumMoleculeInstrumentationElectron ionizationVacuum
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Competing salt effects on phase behavior of protein solutions: tailoring of protein interaction by the binding of multivalent ions and charge screeni…

2014

The phase behavior of protein solutions is affected by additives such as crowder molecules or salts. In particular, upon addition of multivalent counterions, a reentrant condensation can occur; i.e., protein solutions are stable for low and high multivalent ion concentrations but aggregating at intermediate salt concentrations. The addition of monovalent ions shifts the phase boundaries to higher multivalent ion concentrations. This effect is found to be reflected in the protein interactions, as accessed via small-angle X-ray scattering. Two simulation schemes (a Monte Carlo sampling of the counterion binding configurations using the detailed protein structure and an analytical coarse-grain…

chemistry.chemical_classificationIonsCondensationOsmolar ConcentrationSurfaces Coatings and FilmsIonProtein–protein interactionProtein structurechemistryX-Ray DiffractionIonic strengthComputational chemistryPhase (matter)Scattering Small AngleMaterials ChemistryMoleculeHumansSaltsPhysical and Theoretical ChemistryCounterionSerum AlbuminThe journal of physical chemistry. B
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Absorption and desorption of liquid water by a superabsorbent polymer: Effect of polymer in the drying of the soil and the quality of certain plants

2001

In this work, we were interested in the study of the kinetic behavior of the reaction of drying soil representing the Marrakesh region (south of Morocco) in the presence of an superabsorbent polymer. The presence of a polymer in the soil diminished the kinetic drying of the soil, which will have as an application a reduction in water loss in the process of irrigation. The presence of a polymer in the soil enables a complete modification of the kinetic regimes controlling the soil-drying kinetic. We also realized the first study of the behavior of certain selected plants in the melange of a soil and a polymer. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 234–243, 2002

chemistry.chemical_classificationIrrigationAbsorption of waterPolymers and PlasticsGeneral ChemistryPolymerPolyelectrolyteSurfaces Coatings and FilmschemistrySuperabsorbent polymerChemical engineeringDesorptionSoil waterMaterials ChemistryOrganic chemistryAbsorption (chemistry)Journal of Applied Polymer Science
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Absorption and desorption of liquid water by a superabsorbent polyelectrolyte: Role of polymer on the capacity for absorption of a ground

2001

To study the potentialities of a polyelectrolyte superabsorbent for the storage of water, we have studied a ground representative of the area of Haouz (area of Marrakesh, South of Morocco) in the presence of polymer. We sought the optimal proportions allowing the best retention of water by the mixture made up of the polymer and the ground and to prolong the storage period of water in the ground. We have also studied the effect of certain ions and the pH on the capacity for absorption of polymer. These ions can be naturally present in the ground or introduced by the means of manure and pesticides. The presence of polymer in the ground makes it possible to increase the capacity for absorption…

chemistry.chemical_classificationIrrigationAbsorption of waterPolymers and PlasticsInorganic chemistryGeneral ChemistryPolymerPolyelectrolyteSurfaces Coatings and FilmsIonInfiltration (hydrology)chemistryDesorptionMaterials ChemistrymedicineSwellingmedicine.symptomJournal of Applied Polymer Science
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Inhibitoren der Korrosion 23 (1) - Gibt es eine Struktur- Wirkungs-Beziehung bei organischen Inhibitoren der Korrosion von Aluminium?

1978

Uber 400 organische Verbindungen wurden routinemasig darauf gepruft, ob sie die Auflosung des Aluminiums in In Salzsaure in Gegenwart von 2,5% NaCl und bei einer Konzentration von 10−2 Mol/l der zu prufenden Verbindung beeinflussen. Es wurde versucht, eine “Struktur-Wirkungs-Beziehung” zu erstellen. Eingehender diskutiert wurden folgende Verbindungsklassen: Arsenverbindungen, Phosphon- und Phosphinsauren, aromatische Aldehyde und Ketone, aromatische und aliphatische Carbonsauren, zweiwertige Phenole, Tetrazoliumsalze und formazane, Sulfoxide und aromatische Sulfonsauren, Sulfonamide und Sulfone. Bei einer Auswahl von Inhibitoren wurde die Abhangigkeit der Schutzwirkung von deren Konzentrati…

chemistry.chemical_classificationKetoneMechanical EngineeringMetals and Alloyschemistry.chemical_elementSulfoxideGeneral MedicineZincAldehydeMedicinal chemistryOrganic compoundSurfaces Coatings and FilmsSulfonamideSulfonechemistry.chemical_compoundchemistryMechanics of MaterialsPolymer chemistryMaterials ChemistryEnvironmental ChemistryPhenolsMaterials and Corrosion/Werkstoffe und Korrosion
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The first structurally characterized cationic lanthanide–alkyl complexesElectronic supplementary information (ESI) available: experimental and spectr…

2002

Reaction of rare earth metal–alkyl complexes [Ln(CH2SiMe3)3(THF)2] (Ln = Y, Lu) with B(C6X5)3 (X = H, F) in the presence of crown ethers gives crystallographically characterized ion pairs [Ln(CH2SiMe3)2(CE)(THF)n]+[B(CH2SiMe3)(C6X5)3]– (CE = [12]-crown-4, n = 1; CE = [15]-crown-5 and [18]-crown-6, n = 0).

chemistry.chemical_classificationLanthanideStereochemistryRare earthMetals and AlloysCationic polymerizationGeneral ChemistryIon pairsMedicinal chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryMaterials ChemistryCeramics and CompositesAlkylChemical Communications
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Kinetics of Molecule Transfer between Lipid Vesicles and β-Cyclodextrins

1996

Abstract We propose a calorimetric method based on the van't Hoff model of depression of the freezing temperature to investigate slow kinetics involving lipid vesicles (liposomes) and drug–β-cyclodextrin (Cyd) complexes. Some nonsteroidal antiinflammatory drugs (NSAIDs) were examined and standard phospholipid liposomes were used in our experiments. Three different kinetic processes were investigated: (a)9Transfer of drugs from water-soluble Cyd-complexes to void liposomes. (b)9Uptake of drugs from the surface of liposomes by free Cyd dissolved in the aqueous phase. (c)9Exchange of drugs from loaded to void vesicles, and the effect of free Cyd in enhancing such a transfer. Most experiments w…

chemistry.chemical_classificationLiposomeChromatographyCyclodextrinChemistryVesicleBilayerKineticsPhospholipidSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsInclusion compoundBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryDifferential scanning calorimetryBiophysicsJournal of Colloid and Interface Science
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Butene Isomerization and Double-Bond Migration on the H-ZSM-5 Outer Surface: A Density Functional Theory Study

2011

Isomerization of trans-but-2-ene to cis-but-2-ene and double bond migration of trans-but-2-ene to but-1-ene have been investigated by means of density functional theory calculations on a suitable model of H-ZSM-5 surface. The study has been afforded on outer surface sites by considering the hydroxyl group of either a SiO2(OH)2 or a AlO2H(OH)2 moiety. On these outer surface sites, one alkoxide species occurs as a stable intermediate both along the isomerization and double bond migration pathways. The latter process could also occur via a single-step mechanism, which involves a six-center transition state. The energy barriers of the outer surface processes above do not take any advantage by t…

chemistry.chemical_classificationMFI zeolite outer surface DFTDouble bondHydrogenchemistry.chemical_elementPhotochemistryButeneSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundGeneral EnergychemistryAlkoxideMoietyDensity functional theoryPhysical and Theoretical ChemistryZSM-5IsomerizationThe Journal of Physical Chemistry C
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Phase Separation and Nematic Order in Lyotropic Solutions: Two Types of Polymers with Different Stiffnesses in a Common Solvent

2021

The interplay of the isotropic-nematic transition and phase separation in lyotropic solutions of two types of semiflexible macromolecules with pronounced difference in chain stiffness is studied by Density Functional Theory and Molecular Dynamics simulations. While the width of the isotropic-nematic two-phase coexistence region is narrow for solutions with a single type of semiflexible chain, the two-phase coexistence region widens for solutions containing two types of chains with rather disparate stiffness. In the nematic phase, both types of chains contribute to the nematic order, with intermediate values of the order parameter compared to the corresponding single component solutions. As …

chemistry.chemical_classificationMaterials science010304 chemical physicsPolymer010402 general chemistry01 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsCondensed Matter::Soft Condensed MatterMolecular dynamicsChain (algebraic topology)chemistryChemical physicsLiquid crystalPhase (matter)Bending stiffness0103 physical sciencesLyotropicMaterials ChemistryDensity functional theoryPhysical and Theoretical ChemistryThe Journal of Physical Chemistry B
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