Search results for "Caprolactone"

showing 10 items of 72 documents

Rapid One-Step Fabrication of Graphene Oxide-Decorated Polycaprolactone Three-Dimensional Templates for Water Treatment

2020

Coating of flexible substrates is crucial to prepare versatile, multifunctional materials. However, exploration of effective fabrication approaches is still a challenging issue, because the pathways generally proposed require time-consuming, multistep protocols. Here, we developed a one-pot process for decorating either pearl necklace-like or fibrous fluffy-like structures of polycaprolactone (PCL) with graphene oxide (GO) skin. PCL solutions were dry jet-wet electrosprayed or electrospun into a stirred liquid collector constituted by ethanol-containing GO nanoparticles. The stirred liquid collector enables the formation of 3D-structures, whose microarchitecture can be designed by controlli…

Materials scienceFabricationPolymers and PlasticsOxideNanotechnologyOne-Stepengineering.materialfiberslaw.inventionchemistry.chemical_compoundCoatinglawdry jet-wet-electrospinning3D electrospinningGrapheneProcess Chemistry and TechnologyOrganic Chemistrybeadsgraphene coatingSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiTemplatechemistryphenol removalhierarchical structurePolycaprolactoneengineeringWater treatment
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Diene/polar monomer copolymers, compatibilisers for polar/non-polar polymer blends. A controlled block copolymerisation with a single-site component …

2002

A well-controlled two-step process, the polymerisation of isoprene or isoprene/hex-1-ene copolymerisation followed by e-caprolactone polymerisation, affords trans-polyisoprene or (trans-polyisoprene/hex-1-ene copolymer)–poly(e-caprolactone) diblocks of various lengths. The single component initiator is an allylsamarocene compound. An atomic force microscopy study shows that these copolymers are efficient compatibilisers for poly(e-caprolactone) and polyisoprene blends. Poly(e-caprolactone) chain growth from Sm–polyisoprene chain.

Materials sciencePolymers and PlasticsDieneOrganic ChemistryCompatibilizationCondensed Matter Physicschemistry.chemical_compoundMonomerchemistryPolymerizationPolycaprolactonePolymer chemistryMaterials ChemistryCopolymerPolymer blendPhysical and Theoretical ChemistryIsopreneMacromolecular Chemistry and Physics
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Characterizations of Thermoplastic Block Elastomers Based on Polybutadiene and ε -Caprolactone

2010

A broad series of tri- and multiblock copolymers based on linear and branched oligomers of polybutadiene as central blocks and polycaprolactone (PCL) as block extremities are characterized by SEC, DSC, DMA, Dynamical Rheology and DRX. DSC analyses reveal phase separation between the two amorphous PB and PCL phases. By thermal analysis, the glass transition temperature of PCL is only detected for materials containing at least 80% w/w of PCL. This is attributed to the small length of the polyester blocks for copolymers containing less than 80% w/w of PCL. The increase of fusion heat with increasing PCL content in the copolymers is correlated to the greater ability of PCL chains to rearrange a…

Materials sciencePolymers and PlasticsEnthalpy of fusionGeneral ChemistryDynamic mechanical analysisElastomerchemistry.chemical_compoundPolybutadienechemistryPolycaprolactoneMaterials ChemistryCeramics and CompositesThermoplastic elastomerComposite materialGlass transitionCaprolactoneJournal of Macromolecular Science, Part A
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Tunable release of Chlorhexidine from Polycaprolactone-based filaments containing graphene nanoplatelets

2019

Abstract Graphene nanoplatelets (GNP) as fillers and Chlorhexidine (CHX), as an antibacterial agent, were incorporated in a polycaprolactone (PCL) matrix and processed into filaments by melt spinning. The influence of both drawing and formulation on the processability, spinnability, mechanical properties and release behaviour of these materials were deeply investigated by performing rheological, morphological analysis, tensile tests, and by measuring the cumulative release of CHX in PBS at 37 °C. Furthermore, Korsmeyer–Peppas model was adopted to study the kinetics release mechanism. The results showed that adding GNP did not alter the processability and spinnability of the systems. Further…

Materials sciencePolymers and PlasticsGeneral Physics and Astronomy02 engineering and technology010402 general chemistry01 natural scienceslaw.inventionchemistry.chemical_compoundRheologylawUltimate tensile strengthMaterials ChemistryControlled releaseComposite materialAntibacterial agentNanocompositeNanocompositeGrapheneOrganic Chemistry021001 nanoscience & nanotechnologyControlled release0104 chemical sciencesMelt spinningSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryPCLPolycaprolactoneMelt spinningGraphene0210 nano-technologyMechanical propertie
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Polycaprolactone-based scaffold for oil-selective sorption and improvement of bacteria activity for bioremediation of polluted water

2017

Abstract A novel floatable and biodegradable sponge for the selective absorption of oil from water and potentially useful as cell carrier for bioremediation treatments was prepared in polycaprolactone (PCL). The eco-friendly process for fabricating the PCL sponge does not involve either synthetic routes or organic solvents, thus minimizing environmental hazard. In particular, the 3D porous materials have been prepared by mixing in the melt the polymer matrix with two water-soluble porogen agents (NaCl and PEG) and thereafter leaching the obtained PCL/NaCl/PEG composites in water. The PCL sponges here proposed are capable to remove different types of oily pollutants (up to 500 wt%), and were…

Materials sciencePolymers and PlasticsGeneral Physics and Astronomy02 engineering and technology010501 environmental sciences01 natural scienceschemistry.chemical_compoundBioremediationPEG ratioMaterials ChemistryComposite material0105 earth and related environmental sciencesAlkanechemistry.chemical_classificationbiologyOrganic Chemistrytechnology industry and agricultureSorption021001 nanoscience & nanotechnologybiology.organism_classificationHydrocarbonchemistryPolycaprolactoneLeaching (metallurgy)Alcanivorax0210 nano-technologyEuropean Polymer Journal
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Synthesis and degradation of poly (2-hydroxyethyl methacrylate)-graft-poly (ε-caprolactone) copolymers

2004

Abstract Poly (e-caprolactone) macromonomers carrying a methacryloyl end groups were synthesized using different lanthanide derivatives as catalysts, and characterized by SEC and 1 H NMR. Hydrophilic–hydrophobic copolymers from macromonomers and 2-hydroxyethyl methacrylate (HEMA) were obtained by solution free radical polymerization. Depending on the feed ratio of the two components, different copolymer structures were obtained. The expected graft structure of the copolymers was confirmed by 1 H NMR. Thermal properties of the copolymers were determined by DSC and TGA. Hydrolytic and enzymatic degradations of the materials were performed. Poly (2-hydroxyethyl methacrylate)- graft -poly (e-ca…

Materials sciencePolymers and PlasticsRadical polymerizationtechnology industry and agricultureCationic polymerizationCondensed Matter PhysicsMethacrylateMacromonomerRing-opening polymerizationchemistry.chemical_compoundchemistryMechanics of MaterialsPolycaprolactonePolymer chemistryMaterials ChemistryCopolymerCaprolactonePolymer Degradation and Stability
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Polycaprolactone/gelatin-based scaffolds with tailored performance: in vitro and in vivo validation

2019

Abstract Nanofibrous scaffolds composed of polycaprolactone (PCL) and gelatin (Ge) were obtained through a hydrolytic assisted electrospinning process. The PCL-to-Ge proportion (100/0 to 20/80), as well as the dissolution time (24, 48, 72, 96, 120 h) into a 1:1 formic/acetic acid solvent before electrospinning were modified to obtain the different samples. A strong influence of these factors on the physicochemical properties of the scaffolds was observed. Higher Ge percentage reduced crystallinity, allowed a uniform morphology and increased water contact angle. The increase in the dissolution time considerably reduced the molar mass and, subsequently, fibre diameter and crystallinity were a…

Materials sciencefood.ingredientBiocompatibilityPolyestersMyocardial InfarctionNanofibersBioengineering02 engineering and technology010402 general chemistry01 natural sciencesGelatinCell LineScaffoldBiomaterialsContact angleMiceCrystallinitychemistry.chemical_compoundfoodMaterials TestingCell AdhesionAnimalsHumansTailoredRats WistarMaterialsDissolutionCells CulturedCell ProliferationMolar massTissue EngineeringTissue ScaffoldsMyocardiumin vitro021001 nanoscience & nanotechnologyElectrospinningRats0104 chemical sciencesMice Inbred C57BLDisease Models Animalin vivochemistryChemical engineeringMechanics of MaterialsPolycaprolactoneLeukocytes MononuclearGelatinBiocompatibility0210 nano-technologyMaterials Science and Engineering: C
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1-n-Butyl-3-methylimidazolium-2-carboxylate: a versatile precatalyst for the ring-opening polymerization of ε-caprolactone and rac-lactide under solv…

2013

The ring-opening polymerization of ε-caprolactone (ε-CL) and rac-lactide (rac-LA) under solvent-free conditions and using 1-n-butyl-3-methylimidazolium-2-carboxylate (BMIM-2-CO2) as precatalyst is described. Linear and star-branched polyesters were synthesized by successive use of benzyl alcohol, ethylene glycol, glycerol and pentaerythritol as initiator alcohols, and the products were fully characterized by 1H and 13C{1H} NMR spectroscopy, gel permeation chromatography (GPC), and differential scanning calorimetry (DSC). BMIM-2-CO2 acts as an N-heterocyclic carbene precursor, resulting from in situ decarboxylation, either by heating under vacuo (method A) or by addition of NaBPh4 (method B)…

N-heterocarbene precursorLactideLetterOrganic ChemistryRing-opening polymerizationPentaerythritollcsh:QD241-441chemistry.chemical_compoundChemistryimidazolium-2-carboxylateschemistryPolymerizationlcsh:Organic chemistryBenzyl alcoholgreen polymerization reactionPolymer chemistryaliphatic polyestersOrganic chemistrylcsh:QorganocatalysisCarboxylatelcsh:ScienceCaprolactoneEthylene glycolBeilstein Journal of Organic Chemistry
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Mechanism of nanocapsules formation by the emulsion-diffusion process.

2007

International audience; A detailed investigation into the mechanisms of nanocapsule formation by means of the two stages “emulsion–diffusion” process is reported. Such widely used process is still poorly understood. An emulsion of oil, polymer and ethyl acetate is fabricated as a first step; dilution with pure water allows ethyl acetate to diffuse out from the droplets, leaving a suspension of nanocapsules at the end. It has been shown that the size of nanocapsules was related to the chemical composition of the organic phase and the size of primary emulsion through a simple geometrical relationship. As a consequence, most of the properties of the nanocapsules were decided at the emulsificat…

NanocapsuleDiffusionEthyl acetate02 engineering and technologyEmulsion–diffusion010402 general chemistry01 natural sciencesNanocapsulesSuspension (chemistry)Biomaterialschemistry.chemical_compoundColloid and Surface ChemistryPhase (matter)Polymer chemistry[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process Engineeringchemistry.chemical_classificationEmulsionAqueous two-phase systemPolymer021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsPolycaprolactoneProcesschemistryChemical engineeringEmulsion0210 nano-technologyJournal of colloid and interface science
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Production of polymeric micro- and nanostructures with tunable properties as pharmaceutical delivery systems

2020

Abstract The production of novel graft copolymers based on poly-e-caprolactone (PCL) and polyaspartamide are useful to realize structures for potential biomedical applications. Here, the synthesis of pegylated PCL/polyhydroxyethyl aspartamide (PHEA) graft copolymers (PHEA-g-SUCC-PCL-g-PEG) with tunable composition, was achieved by followpling a synthetic strategy that involved first the grafting of preformed PCL on PHEA backbone, then polyethylen glycol (PEG), by using 1,1′-carbonyldiimidazole (CDI) to speed up the condensation reaction. Graft copolymers with a Derivatization Degree (DD) in PCL ranging between 1.1 and 4.4 mol% were obtained, and processable with different technologies for t…

NanostructureMaterials sciencePolymers and PlasticsMicrofluidicsNanoparticlemacromolecular substances02 engineering and technology010402 general chemistry01 natural sciencesPEG ratioMaterials ChemistryCopolymerOrganic Chemistrytechnology industry and agricultureαβ-poly(N-2-hydroxyethyl)-DL-aspartamide (PHEA)equipment and suppliesmusculoskeletal system021001 nanoscience & nanotechnologyCondensation reactionGrafting0104 chemical sciencesGraft copolymerChemical engineeringMicrofluidicMicroparticlePoly-ε-caprolactone (PCL)Settore CHIM/09 - Farmaceutico Tecnologico ApplicativoNanoparticles0210 nano-technologyNanoprecipitation
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