Search results for "modification"

showing 10 items of 853 documents

Utilisation of barium-modified analcime in sulphate removal: Isotherms, kinetics and thermodynamics studies

2017

Abstract Analcime and commercial zeolite were employed as a precursor for preparing sorbent material for SO42− removal over barium modification. Three sorbents were prepared: barium-modified analcime (ANA-Na-Ba), barium-modified acid-washed analcime (ANA-Ac-Na-Ba) and barium-modified zeolite (ZSM5-Na-Ba). Of the prepared materials, ANA-Ac-Na-Ba was the most efficient sorbent material for SO42− removal, with a maximum sorption uptake of 13.7 mg g−1 at room temperature. Batch sorption experiments were performed to evaluate the effect of initial pH, initial SO42− concentration, sorbent dosage, temperature and contact time of sorption. Several isotherms were applied to describe the experimental…

SorbentAnalcimeProcess Chemistry and TechnologyKineticsInorganic chemistryChemical modificationchemistry.chemical_elementBariumSorption02 engineering and technology010501 environmental sciencesengineering.material021001 nanoscience & nanotechnology01 natural sciencesAdsorptionchemistryChemical engineeringengineering0210 nano-technologySafety Risk Reliability and QualityZeoliteWaste Management and Disposal0105 earth and related environmental sciencesBiotechnologyJournal of Water Process Engineering
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Reactive surface coatings based on polysilsesquioxanes: universal method toward light-responsive surfaces.

2011

Reactive surface coatings were used as an ideal precursor coating for the fabrication of three different photoswitchable surface coatings in parallel. Different light-responsive moieties, such as azobenzene, salicylideneaniline, and spiropyran, were immobilized on glass, polycarbonate, and steel surfaces. Independent from the underlying substrate, wettability could be switched reversibly by UV irradiation. The maximum switching range was obtained after functionalization of the reactive coating with spiropyran, resulting in a contact angle difference between the two isomeric states of almost 30°.

SpiropyranMaterials scienceSubstrate (electronics)engineering.materialPhotochemistryContact anglechemistry.chemical_compoundCoatingAzobenzenechemistryvisual_artengineeringvisual_art.visual_art_mediumSurface modificationGeneral Materials ScienceWettingPolycarbonateACS applied materialsinterfaces
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La clause de non-concurrence introduite dans les statuts ultérieurement à la création de la société ne peut être décidée qu'à l'unanimité des actionn…

1996

International audience

Statuts[SHS.DROIT]Humanities and Social Sciences/Law[SHS.DROIT] Humanities and Social Sciences/LawSOCIETE COMMERCIALEOpposabilitéAssemblée généraleModificationComputingMilieux_MISCELLANEOUS
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ChemInform Abstract: Synthesis and Functionalization of Chalcogenide Nanotubes

2011

New synthetic approaches to MS 2 (M = Sn, Nb, Mo, W) chalcogenide nanostructures are highlighted. Most chalcogenide particles can be functionalized directly with inorganic nanoparticles such as Au, ZnO or MnO. Depending on the Pearson hardness of the metal involved, the functionalization may be reversible or irreversible. A covalent functionalization strategy is based on a steric shielding of the coordination sphere of transition metal atoms in such a way that only coordination sites are available for bonding to the chalcogenide surface. This allows the immobilization of fluorophors, redox active groups or proteins onto chalcogenide nanoparticle.

Steric effectsNanostructureCoordination sphereChalcogenideNanoparticleGeneral MedicineMetalChalcogenchemistry.chemical_compoundchemistryChemical engineeringvisual_artvisual_art.visual_art_mediumSurface modificationChemInform
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DFT studies of COOH tip-functionalized zigzag and armchair single wall carbon nanotubes

2011

Structure and energy calculations of pristine and COOH-modified model single wall carbon nanotubes (SWCNTs) of different length were performed at B3LYP/6-31G* level of theory. From 1 to 9 COOH groups were added at the end of the nanotube. The differences in structure and energetics of partially and fully functionalized SWCNTs at one end of the nanotube are observed. Up to nine COOH groups could be added at one end of (9,0) zigzag SWCNT in case of full functionalization. However, for (5,5) armchair SWCNT, the full functionalization was impossible due to steric crowding and rim deformation. The dependence of substituent attachment energy on the number of substituents at the carbon nanotube ri…

Steric effectsNanotubeMaterials scienceBiomedicine generalCarboxylic AcidsSubstituentHealth InformaticsCarbon nanotubeDFTCatalysislaw.inventionEnd-substitutionInorganic Chemistrychemistry.chemical_compoundCarboxylation energylawOrganic chemistryComputer SimulationComputer Applications in ChemistryPhysical and Theoretical ChemistryAnthracenesLife Sciences generalOriginal PaperNanotubes CarbonOrganic ChemistryZigzag and armchair SWCNTBenzoic AcidPhenanthrenesComputer Science ApplicationsChemistryCrystallographyModels ChemicalComputational Theory and MathematicschemistryZigzagComputer Appl. in Life SciencesQuantum TheoryThermodynamicsMolecular MedicineSurface modificationCOOH functionalization
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Synthesis and functionalization of chalcogenide nanotubes

2010

New synthetic approaches to MS 2 (M = Sn, Nb, Mo, W) chalcogenide nanostructures are highlighted. Most chalcogenide particles can be functionalized directly with inorganic nanoparticles such as Au, ZnO or MnO. Depending on the Pearson hardness of the metal involved, the functionalization may be reversible or irreversible. A covalent functionalization strategy is based on a steric shielding of the coordination sphere of transition metal atoms in such a way that only coordination sites are available for bonding to the chalcogenide surface. This allows the immobilization of fluorophors, redox active groups or proteins onto chalcogenide nanoparticle.

Steric effectsNanotubeMaterials scienceNanostructureCoordination sphereChalcogenideNanoparticleNanotechnologyCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsMetalchemistry.chemical_compoundChemical engineeringchemistryvisual_artvisual_art.visual_art_mediumSurface modificationphysica status solidi (b)
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Molecular recognition processes at functionalized lipid surfaces: a neutron reflectivity study

1992

The specific binding of proteins to functionalized monolayers on aqueous subphases has been characterized by neutron reflectivity measurements. As a model for the investigation of a recognition process on a molecular length scale, streptavidin (SA) and biotin were chosen because of the high specific affinity between them. Reflectivities from the aqueous (NaCl/H2O or NaCl/D2O) surfaces covered with the biotin-lipid monolayers before and after the adsorption of proteins were collected with a novel, fixed wavelength liquid surface neutron reflectometer. In quantitative terms, binding was found to occur at a biotin surface concentration as low as 1 molecule/1250 A2 (compare to ∼ 1 molecule/40 A…

StreptavidinChromatographyAqueous solutionChemistryMetals and AlloysAnalytical chemistrySurfaces and InterfacesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundMolecular recognitionAdsorptionMonolayerMaterials ChemistryMoleculeSurface modificationNeutronThin Solid Films
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Reactive Surface Coatings Based on Polysilsesquioxanes: Controlled Functionalization for Specific Protein Immobilization

2009

The key designing in reliable biosensors is the preparation of thin films in which biomolecular functions may be immobilized and addressed in a controlled and reproducible manner. This requires the controlled preparation of specific binding sites on planar surfaces. Poly(methylsilsesquioxane)-poly(pentafluorophenyl acrylates) (PMSSQ-PFPA) are promising materials to produce stable and adherent thin reactive coatings on various substrates. Those reactive surface coatings could be applied onto various materials, for example, gold, polycarbonate (PC), poly(tetrafluoroethylene) (PTFE), and glass. By dipping those substrates in a solution of a desired amine, specific binding sites for protein ads…

StreptavidinMaterials sciencePolymersSurface PropertiesBiotinInfrared spectroscopyMicroscopy Atomic Forcechemistry.chemical_compoundAdsorptionSpectroscopy Fourier Transform InfraredElectrochemistryOrganic chemistryBiotinylationOrganosilicon CompoundsGeneral Materials ScienceFourier transform infrared spectroscopySurface plasmon resonanceFuransPolytetrafluoroethyleneSpectroscopyPolycarboxylate CementTemperaturetechnology industry and agricultureProteinsSurfaces and InterfacesCondensed Matter PhysicsAmidesQuaternary Ammonium CompoundsModels ChemicalchemistryChemical engineeringSurface modificationGlassBiosensorProtein adsorptionLangmuir
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Streptavidin-coated TiO2 surfaces are biologically inert: Protein adsorption and osteoblast adhesion studies

2011

Non-fouling TiO2 surfaces are attractive for a wide range of applications such as biosensors and medical devices, where biologically inert surfaces are needed. Typically, this is achieved by controlled surface modifications which prevent protein adsorption. For example, polyethylene glycol (PEG) or PEG-derived polymers have been widely applied to render TiO2 surfaces biologically inert. These surfaces have been further modified in order to achieve specific bio-activation. Therefore, there have been efforts to specifically functionalize TiO2 surfaces with polymers with embedded biotin motives, which can be used to couple streptavidin for further functionalization. As an alternative, here a s…

StreptavidinMaterials scienceSurface PropertiesBiomedical EngineeringNanotechnologyMicroscopy Atomic ForceCell LineBiomaterialschemistry.chemical_compoundCell AdhesionHumansBiotinylationTitaniumchemistry.chemical_classificationOsteoblaststechnology industry and agricultureMetals and AlloysPolymerSilanesFibronectinsKineticsSurface coatingchemistryBiotinylationCeramics and CompositesSurface modificationMuramidaseAdsorptionStreptavidinBiosensorLayer (electronics)Protein adsorptionJournal of Biomedical Materials Research Part A
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Surface functionalization and surface recognition: Plasmon optical detection of molecular recognition at self assembled monolayers

1991

The synthesis of biotin- functionalized organic mercaptans and their chemisorption on gold surfaces is described. Biotin bound covalently to self assembled monolayers is recognized by streptavidin from aqueous buffer solutions. Spacer length and packing density of the biotin labels on the organic surface determine the docking kinetics. With a flexible and hydrophilic spacer very fast -diffusion controlled-docking is observed. As an alternative method of self assembly the spreading of organic mercaptans on water surfaces is established. Pressure-area diagrams of different functionalized mercaptans and disulfides are shown and their monolayer properties are discussed.

StreptavidinPolymers and PlasticsChemistryOrganic ChemistrySelf-assembled monolayerCondensed Matter PhysicsCombinatorial chemistrychemistry.chemical_compoundMolecular recognitionChemisorptionMonolayerMaterials ChemistryOrganic chemistrySurface modificationSelf-assemblyPlasmonMakromolekulare Chemie. Macromolecular Symposia
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