Search results for "cyclophosphazene"

showing 7 items of 7 documents

TI: Cyclophosphazenes as polymer modifiers

2003

The utilization of cyclophosphazenes as polymer modifiers is reviewed, with particular concern to their exploitation as versatile chain extenders, possibly for recycle problems, crosslinkers, to enhance mechanical properties of polymeric materials, branchers, to selectively introduce ramifications in linear polymers, and compatibilizers, to favor the formation of blends between originally incompatible organic macromolecules. The great versatility of the synthetic methods put forward for these substrates, together with the ease of controlling their modification, functionalization and reactivity are important parameters for the evaluation of which type of use is more feasible for these trimer…

chemistry.chemical_classificationchain-extender2-oxazolineMaterials sciencePolymers and PlasticsPolymer scienceLinear polymerOrganic ChemistryPolymerCondensed Matter Physicschemistry.chemical_compoundSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryMaterials ChemistrycyclophosphazeneepoxideSurface modificationOrganic chemistrycompatibilizerReactivity (chemistry)AzideMacromolecule
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New phosphazene-based chain extenders containing allyl and epoxide groups

2003

In this paper we present the synthesis and the characterization of cyclophosphazenes substituted with allyl groups, their transformation in epoxide-containing cyclophosphazenes and the final utilization of these compounds as chain extenders in combination with polyamides. The reaction at high temperature of Nylon-6 with epoxy-functionalized cyclophosphazenes leads to the opening of the epoxy units by the action of both amino (--NH2) and carboxylic (--COOH) end-groups of the polymer to enhance the final molecular weight of this material. The consequences of this fact on the thermal, mechanical and visco-elastic properties of treated Nylon-6 have been also evaluated and compared to those of t…

Polymers and PlasticsGeneral Chemical EngineeringEpoxidechemistry.chemical_compoundPolymer chemistryMaterials ChemistryOrganic chemistryThermal stabilityPhosphazenechemistry.chemical_classificationchain extensionpolyamideGeneral ChemistryEpoxyPolymerNMREnd-groupSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiNylon 6chemistryvisual_artPolyamidecyclophosphazeneNylon-6; cyclophosphazenes; chain extension; polyamides; NMR.visual_art.visual_art_mediumnylon-6Designed Monomers and Polymers
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Reactions Occurring during the Melt Mixing of Nylon 6 and Oxazoline−Cyclophosphazene Units

2009

Specific reactions of amino and carboxyl end groups of Nylon 6 with the reactive oxazoline groups belonging to a cyclophosphazene compound (referred as CP20XA) were carried out at 240 °C for different times, under inert atmosphere. Ny6 polymers terminated with one specific reactive chain end (-COOH or NH2) were reacted with different amounts of CP20XA to study the kinetic order of the reactions. All Ny6-CP20XA reacted products soluble in trifluoroethanol (TFE) were well characterized by MALDI-TOF MS, FT-IR and ( 1H and 13C) NMR techniques. The MALDI-TOF results show that the oxazoline rings react with the carboxyl chain ends of Ny6 following second-order kinetics. The reactions with amino c…

chemistry.chemical_classificationOxazolineReaction mechanismPolymers and PlasticsOrganic ChemistryKineticsSide reactionPolymerOxazolineReactive BlendingInorganic Chemistrychemistry.chemical_compoundEnd-groupSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiNylon6Nylon 6chemistrycyclophosphazenes polyamide end-functionalization MALDI-TOFMaterials ChemistryOrganic chemistryInert gasMALDIMacromolecules
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Chemical Reactions occurring in the molten state between Ny6 and Oxazoline groups linked to a Cyclophosphazene moiety

2009

Settore ING-IND/22 - Scienza E Tecnologia Dei Materialicyclophosphazenes polyamide end-functionalization MALDI-TOF
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Cyclo- and Polyphosphazenes for Biomedical Applications

2022

Cyclic and polyphosphazenes are extremely interesting and versatile substrates characterized by the presence of -P=N- repeating units. The chlorine atoms on the P atoms in the starting materials can be easily substituted with a variety of organic substituents, thus giving rise to a huge number of new materials for industrial applications. Their properties can be designed considering the number of repetitive units and the nature of the substituent groups, opening up to a number of peculiar properties, including the ability to give rise to supramolecular arrangements. We focused our attention on the extensive scientific literature concerning their biomedical applications: as antimicrobial age…

polyphosphazenesOrganic ChemistryPharmaceutical SciencepolyphosphazeneAnalytical Chemistrycyclophosphazenes; drug delivery; polyphosphazenes; tissue engineeringChemistry (miscellaneous)Settore CHIM/03 - Chimica Generale E Inorganicatissue engineeringDrug Discoverydrug deliverycyclophosphazenescyclophosphazeneMolecular MedicinePhysical and Theoretical Chemistry
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Effect of adding new phosphazene compounds to poly(butylene terephthalate)/polyamide blends. I: Preliminary study in a batch mixer

2005

Abstract Poly(butylene terephthalate) (PBT) and a sample of polyamide have been melt processed in the presence of two new phosphazene compounds, namely 2,2-dichloro-4,4,6,6-bis[spiro(2′,2″dioxy-1′,1″biphenyl)]cyclotriphosphazene (2Cl-CP) and 2,2-bis-(2-methoxy-4-methyleneoxy-phenoxy)-4,4,6,6,-bis[spiro(2′,2″dioxy-1′,1″biphenyl)]cyclophosphazene (CP-2EPOX). The blends were prepared by using polyamide 6 (PA6) at 25/75 w/w and 75/25 w/w composition. In order to perform a preliminary analysis on the behaviour of the blends, the materials were prepared in a batch mixer. The materials have been completely characterized from a rheological, morphological, mechanical point of view. The results indic…

PolybutyleneterephthalateReaction mechanismMaterials sciencePolymers and PlasticsCyclophosphazeneCondensed Matter PhysicsViscositychemistry.chemical_compoundSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryRheologyCompatibilisationPolymer blendsMechanics of MaterialsPhase (matter)PolyamidePolymer chemistryPolyamideMaterials ChemistryCopolymerPolymer blendPhosphazenePolymer Degradation and Stability
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Effect of adding new phosphazene compounds to poly(butylene terephthalate)/polyamide blends. II: Effect of different polyamides on the properties of …

2006

Poly(butylene terephthalate) (PBT) and a sample of polyamide have been melt processed in the presence of two new phosphazene compounds, namely 2,2-dichloro-4,4,6,6-bis[spyro(2',2"-dioxy-1',1"-biphenyl)]cyclotriphosphazene (2Cl-CP) and 2,2-bis(2-methoxy-4-methyleneoxy-phenoxy)-4,4,6,6-bis[spyro(2',2"-dioxy-1',1"-biphenyl)]cyclophosphazene (CP-2EPOX). The blends were prepared by using polyamide 6 (PA6) and polyamide 6,6 (PA66) in 25/75 and 75/25 w/w compositions by using a co-rotating twin-screw extruder. The materials have been completely characterized from a mechanical, rheological, and morphological point of view. The results indicate that the additives used cause an increase of the ruptur…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsIzod impact strength testPolymerCompatibilizationPolymer blendCondensed Matter PhysicsCyclophosphazeneReactive compatibilizationchemistry.chemical_compoundSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryPoly(butylene terephthalate)Mechanics of MaterialsPhase (matter)Polymer chemistryPolyamideMaterials ChemistryCopolymerPolyamidePolymer blendPhosphazene
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