Search results for "Chemical modification"

showing 10 items of 87 documents

Blends of nylon 6 with a polyethylene functionalized by photooxidation

1990

An easy and cheap method to prepare functionalized polyethylene is reported in which polyethylene is photooxidized and then melt-blended with nylon. Structural, rheological, and mechanical modifications indicate that carbonyl, formed during photooxidation, and amine groups react giving rise to copolymers which stabilize the blends. Photooxidized polyethylene from waste could be very effective in preparing polyethylene/polyamide blends with improved properties. This new approach improves over current methods in which compatibilization of polyolefines and polyamides is mostly performed by reacting functionalized polyolefines with polyamides in molten state. The functionalization is achieved b…

Materials sciencePolymers and PlasticsChemical modificationGeneral ChemistryCompatibilizationPolyethyleneSurfaces Coatings and Filmschemistry.chemical_compoundNylon 6chemistryPolyamidePolymer chemistryMaterials ChemistryCopolymerSurface modificationMelt flow indexJournal of Applied Polymer Science
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Chemical Modification of Nitrile to Oxazoline Functionality on a Styrene-Acrylonitrile Copolymer in the Melt

1998

Oxazoline is a very interesting functionality for reactive extrusion and other applications. In this paper, we report the possibility of chemically transforming nitrile group attached to a copolymer of styrene and acrylonitrile (SAN) to oxazoline group using 2-amino-ethanol (AE). The chemical modification of SAN with AE was done in the molten state. Among various catalysts tested, zinc acetate turned out to be the most efficient. The effects of the catalyst concentration, temperature and mixing on the overall kinetics were studied. The formation of the expected oxazoline functionality was confirmed by infrared spectroscopy and by reacting with 1-naphthylacetic acid. The reaction between the…

Materials sciencecompatibilizationPolymers and PlasticsNitrilenitrilepoly-(butylene terephthalate)Chemical modificationGeneral ChemistryReactive extrusionCompatibilizationOxazolineStyrenechemistry.chemical_compoundSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiSANchemistryPolymer chemistryMaterials ChemistryCeramics and CompositesCopolymerOrganic chemistryPolyamide 6AcrylonitrileoxazolineJournal of Macromolecular Science, Part A
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Controlling Multicompartment Morphologies Using Solvent Conditions and Chemical Modification

2016

The solution self-assembly of amphiphilic diblock copolymers into spheres, cylinders, and vesicles (polymersomes) has been intensely studied over the past two decades, and their morphological behavior is well understood. Linear ABC triblock terpolymers with two insoluble blocks A/B, on the other hand, display a richer and more complex morphological spectrum that has been recently explored by synthetic block length variations. Here, we describe facile postpolymerization routes to tailor ABC triblock terpolymer solution morphologies by altering block solubility (solvent mixtures), blending with homopolymers, and block-selective chemical reactions. The feasibility of these processes is demonst…

Materials scienceta114Polymers and PlasticsOrganic ChemistryChemical modification02 engineering and technologyPhysik (inkl. Astronomie)010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesMicelle0104 chemical sciencesInorganic ChemistrySolventchemistry.chemical_compoundchemistryPolymer chemistryPolymersomeAmphiphileMaterials ChemistryCopolymerMethyl methacrylateSolubility0210 nano-technology
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Mixed silane self assembled monolayers and their in situ modification

1998

Mixed self assembled silane monolayers were prepared by coadsorption of Br and methyl terminated trichlorosilanes. By subsequent in situ modification the Br groups were converted into amino groups which can be used to tether polyglutamates to the surface. Here we describe the characterization of the monolayers by means of contact angle measurements and X-ray photoelectron spectroscopy (XPS). Both methods clearly indicate that the Br terminated silane is preferentially adsorbed from the solution. Following the in situ modification by XPS a yield of approximately 80% was determined for the substitution of the bromine by azide, whereas the yield for subsequent reduction to the amine is close t…

Metals and AlloysChemical modificationSelf-assembled monolayerSurfaces and InterfacesSilaneSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsContact anglechemistry.chemical_compoundchemistryX-ray photoelectron spectroscopyMonolayerPolymer chemistryMaterials ChemistryOrganic chemistryAzideMethyl groupThin Solid Films
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Surface Modification of Poly(Vinylchloride) for Manufacturing Advanced Catheters

2017

Polymeric materials, due to their excellent physicochemical properties and versatility found applicability in multiples areas, including biomaterials used in tissue regeneration, prosthetics (hip, artificial valves), medical devices, controlled drug delivery systems, etc. Medical devices and their applications are very important in modern medicine and the need to develop new materials with improved properties or to improve the existent materials is increasing every day. Numerous reasearches are activated in this domain in order to obtain materials/surfaces that does not have drawbacks such as structural failure, calcifications, infections or thrombosis. One of the most used material is pol…

Modern medicineMaterials scienceChemical substanceBiocompatibilityPolymersSurface PropertiesVinyl Chloride030232 urology & nephrologyBiocompatible MaterialsNanotechnology02 engineering and technologySurface finishBiochemistryCatheterization03 medical and health sciencesDrug Delivery Systems0302 clinical medicineDrug DiscoveryPharmacologychemistry.chemical_classificationOrganic ChemistryChemical modificationPolymer021001 nanoscience & nanotechnologychemistryMolecular MedicineSurface modificationWetting0210 nano-technologyCurrent Medicinal Chemistry
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Self-assembly of amphiphilic calixarenes and resorcinarenes in water

2010

The calixarenes and resorcinarenes are macrocyclic phenolic molecules that can be modified “a facon” and a wide range of chemical modification strategies have been published over the last 30 years. Because of their remarkable structural properties and their relative ease of chemical modification, they represent excellent and highly versatile bases to design complex building blocks capable of self-assembly and molecular recognition. They have been widely studied for their ability to form supramolecular structures targeting a wide range of applications. The possibility to regio(rim)-selectively modify these macrocycles with different polar and apolar moieties provides synthetic chemists with …

Molecular recognitionChemistryAmphiphileCalixareneMaterials ChemistrySupramolecular chemistryChemical modificationMoleculeNanotechnologyGeneral ChemistrySelf-assemblyCatalysisNew Journal of Chemistry
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ChemInform Abstract: Self-Assembly of Amphiphilic Calixarenes and Resorcinarenes in Water

2011

The calixarenes and resorcinarenes are macrocyclic phenolic molecules that can be modified “a facon” and a wide range of chemical modification strategies have been published over the last 30 years. Because of their remarkable structural properties and their relative ease of chemical modification, they represent excellent and highly versatile bases to design complex building blocks capable of self-assembly and molecular recognition. They have been widely studied for their ability to form supramolecular structures targeting a wide range of applications. The possibility to regio(rim)-selectively modify these macrocycles with different polar and apolar moieties provides synthetic chemists with …

Molecular recognitionChemistryAmphiphileCalixareneSupramolecular chemistryChemical modificationMoleculeNanotechnologyGeneral MedicineSelf-assemblyChemInform
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Chemical modification of halloysite nanotubes for controlled loading and release.

2020

Clay minerals have been used for medical purposes from ancient times. Among them, the halloysite nanotube, an aluminosilicate of the kaolin group, is an emerging nanomaterial which possesses peculiar chemical characteristics. By means of suitable modifications, such as supramolecular functionalization or covalent modifications, it is possible to obtain novel nanomaterials with tunable properties for several applications. In this context the covalent grafting of suitable organic moieties on the external surface or in the halloysite lumen has been exploited to improve the loading and release of several biologically active molecules. The resulting hybrid nanomaterials have been applied as drug…

NanotubeMaterials scienceTunable properties Controlled drug deliveryHalloysite nanotubeBiomedical EngineeringSupramolecular chemistryNanotechnology02 engineering and technologyengineering.materialChemical characteristic010402 general chemistryYarn Biologically active molecule01 natural sciencesHalloysiteNanomaterialsAluminosilicateKaoliniteGeneral Materials ScienceFunctionalizationGene transferSettore CHIM/02 - Chimica FisicaTargeted drug deliveryCovalent modificationMoleculeGeneral ChemistryGeneral MedicineSettore CHIM/06 - Chimica Organica021001 nanoscience & nanotechnology0104 chemical sciencesNanostructured materialNanotubeSelf-healing hydrogelsengineeringTissue regenerationSurface modificationClay0210 nano-technologyDrug carrierHybrid nanomaterialChemical modificationCovalent graftingJournal of materials chemistry. B
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Silicatein conjugation inside nanoconfined geometries through immobilized NTA–Ni(ii) chelates

2013

The chemical modification and bioconjugation processes inside confined geometries by His-tagged silicatein promote sensitive changes in the polarity and surface charge density that mainly contribute to the ionic current rectification properties of the single conical nanopores.

Nitrilotriacetic AcidPhysics::Biological PhysicsBioconjugationMolecular StructureChemistryMetals and AlloysChemical modificationIonic bondingCharge densityGeneral ChemistryCathepsinsCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsNanoporeChemical engineeringNickelOrganometallic CompoundsMaterials ChemistryCeramics and CompositesNanoparticlesOrganic chemistryChelationChelating AgentsChemical Communications
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Oxazoline functionalization of polyethylenes and their blends with polyamides and polyesters

2001

The compatibilization of blends of polyamide-6 (PA6) with linear low density polyethylene (LLDPE) and of poly(ethylene terephthalate) (PET) with high density polyethylene (HDPE), by functionalization of the polyethylenes with oxazoline groups was investigated. Chemical modification of LLDPE and HDPE was carried out by melt free radical grafting with ricinoloxazoline maleinate. Blends preparation was made either with a two-steps procedure comprising functionalization and blending, and in a single step in which the chemical modification of polyethylene with the oxazoline monomer was realized in situ, during blending. The characterization of the products was carried out by FTIR spectroscopy an…

POLYOLEFINSMaterials sciencePolymers and PlasticsPP/PBTeducationELASTOMERSchemistry.chemical_compoundPOLYMER BLENDSPolymer chemistryMaterials ChemistryPOLYPROPYLENEOrganic Chemistrytechnology industry and agriculturefood and beveragesChemical modificationCompatibilizationPolyethyleneCondensed Matter PhysicsLinear low-density polyethylenePolyesterREACTIVE COMPATIBILIZATIONSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryChemical engineeringSurface modificationHigh-density polyethylenePolymer blendMacromolecular Symposia
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