Search results for "Polymers."

showing 10 items of 3543 documents

Novel Multifunctional Polymeric Photoinitiators and Photo-Coinitiators Derived from Hyperbranched Polyglycerol

2007

A new class of hyperbranched PPIs and PPCs have been prepared. The introduction of compatibilizing groups such as MEEA or trimethylacetate enhanced their solubility in radiation-curable formulations and led to an improved photoactivity compared with the corresponding MPI and MPC. Although the molecular weights of the subject PPIs and PPCs exceeded 800 g mol -1 , the viscosities of the radiation-curable formulations were still suitable for inkjet application. The combination of high photoactivity, low viscosity, and low extract-ability after curing rendered the resulting hyperbranched PPIs and PPCs attractive as components in the inkjet ink for inkjet printing, e.g., in food packaging.

Hyperbranched polyglycerolMaterials sciencePolymers and PlasticsTertiary amineOrganic ChemistryChemical modificationCondensed Matter PhysicsFood packagingEnd-groupPolymer chemistryMaterials ChemistryPhysical and Theoretical ChemistrySolubilityPhotoinitiatorCuring (chemistry)Macromolecular Chemistry and Physics
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Construction and characterization of models of hypercrosslinked polystyrene

2012

A simple algorithm involving classical molecular dynamics (MD) simulations is here suggested to build up models of hypercrosslinked polystyrene showing macroporous structure. The algorithm is composed by three consecutive stages: MD simulation of a single polystyrene coil, crosslink formation, and finally relaxation of the structure. The models, which are differentiated by the crosslinker concentration in the initial polystyrene chain, can be characterized by employing tools of the small angle neutron scattering analysis and procedures associated to the crosslinking algorithm, which allows one to discriminate among the different kinds of crosslinks between phenyl rings and to calculate the …

Hypercrosslinked polystyrene crosslinking degree molecular dynamicsMaterials sciencePolymers and PlasticsRelaxation (NMR)Substrate (chemistry)02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesSmall-angle neutron scattering0104 chemical sciencesCharacterization (materials science)chemistry.chemical_compoundMolecular dynamicsColloid and Surface ChemistryChemical engineeringchemistryPolymer chemistryMaterials ChemistryPolystyrenePhysical and Theoretical Chemistry0210 nano-technologySIMPLE algorithmMacromoleculeColloid and Polymer Science
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Site-specific halloysite functionalization by polydopamine: A new synthetic route for potential near infrared-activated delivery system

2022

Abstract Halloysite nanotubes (HNTs) represent a versatile core structure for the design of functional nanosystems of biomedical interest. However, the development of selective methodologies for the site-controlled functionalization of the nanotubes at specific sites is not an easy task. This study aims to accomplish a procedure for the site-selective/specific, “pin-point”, functionalization of HNTs with polydopamine (HNTs@PDA). This goal was achieved, at pH 6.5, by exploiting the basicity of ZnO nanoparticles anchored on the HNTs external surface (HNTs@ZnO) to induce a punctual polydopamine polymerization and coating. The morphology and the chemical composition of the nanomaterial was demo…

Hyperthermia effectPolydopamineIndolesMaterials sciencePolymersHalloysite nanotubeNanotechnology02 engineering and technologyengineering.material010402 general chemistry01 natural sciencesHalloysiteNanomaterialsBiomaterialsColloid and Surface ChemistryCoatingSecondary modificationDelivery systemNanotubesAqueous solutionSite-specific functionalizationbiologyHalloysite nanotubesHyperthermia effects021001 nanoscience & nanotechnologyGrafting0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsPolymerizationBiotin-avidin interactionbiology.proteinengineeringClaySurface modification0210 nano-technologyAvidinJournal of Colloid and Interface Science
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Mechanical Characterization of Polymers on a Nanometer Scale through Nanoindentation. A Study on Pile-up and Viscoelasticity

2007

The analysis of nanoindentation force curves collected on polymers through the common Oliver and Pharr procedure does not lead to a correct evaluation of Young’s modulus. In particular, the estimated elastic modulus is several times larger than the correct one, thus compromising the possibility of a nanomechanical characterization of polymers. Pile-up or viscoelasticity is usually blamed for this failure, and a deep analysis of their influences is attempted in this work. Piling-up can be minimized by indenting on a true nanometer scale, i.e., at penetration depth smaller than 200 nm. On the other side, it is common knowledge that fast indentations minimize the effect of viscoelasticity. How…

INDENTATION EXPERIMENTSHARDNESSMaterials sciencePolymers and PlasticsTO-RUBBER TRANSITIONModulusNanotechnologyViscoelasticityInorganic ChemistryIndentationMaterials ChemistryLOADComposite materialPenetration depthTEMPERATUREElastic modulusELASTIC-MODULUSOrganic ChemistryNanoindentationCharacterization (materials science)Settore ING-IND/22 - Scienza E Tecnologia Dei MaterialiContact mechanicsRELAXATIONSCRYSTALLIZATIONMETHODOLOGYBEHAVIORMacromolecules
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The Pyridyl Functional Groups Guide the Formation of Pd Nanoparticles Inside A Porous Poly(4-Vinyl-Pyridine)

2015

The reactivity of palladium acetate inside a poly(4-vinylpyridine-co-divinylbenzene) polymer is strongly influenced by the establishment of interaction between the Pd precursor and the pyridyl functional group in the polymer. Diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) and simultaneous X-ray absorption near edge structure (XANES) and small angle X-ray scattering (SAXS) techniques have been applied to monitor the reactivity of palladium acetate in the presence of H-2 and CO as a function of temperature. H-2 reduces palladium acetate to Pd nanoparticles and acetic acid. The pyridyl groups in the polymer play a vital role both in stabilizing the formed acetic acid, thu…

INFRARED-SPECTRADiffuse reflectance infrared fourier transformpolymersmall angle X-ray scatteringInfrared spectroscopychemistry.chemical_elementPALLADIUM(II) ACETATEIR spectroscopy; nanoparticles; palladium; polymers; small angle X-ray scattering; X-ray absorption spectroscopyPhotochemistryCatalysisCatalysisInorganic ChemistryAcetic acidchemistry.chemical_compoundRUTHENIUM NANOPARTICLESPARTICLE FORMATIONENVIRONMENTALLY BENIGNReactivity (chemistry)Physical and Theoretical ChemistryCARBON-MONOXIDEpolymerschemistry.chemical_classificationPOLYMERIC SUPPORTSnanoparticleIN-SITUOrganic ChemistryIR spectroscopy; nanoparticles; palladium; polymers; small angle X-ray scattering; X-ray absorption spectroscopy; Inorganic Chemistry; Organic Chemistry; Physical and Theoretical Chemistry; CatalysisX-ray absorption spectroscopyPolymerpalladiumchemistryIR spectroscopynanoparticlesPalladium(II) acetateTRANSITION-METAL COORDINATIONRESOLVED SAXS ANALYSISPalladium
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Cell uptake enhancement of folate targeted polymer coated magnetic nanoparticles.

2013

Dual targeted drug delivery systems represent a potential platform for developing efficient vector to tumor sites. In this study we evaluated a folate- and magnetic-targeted nanocarriers based on 10 nm iron oxide nanodomais coated with the properly synthesized and characterized folic acid (FA)-functionalized amphiphilic copolymer PHEA-PLA-PEG-FA. FA was chemically conjugated to one end of diamino-polyethylene glycol of 2000 Da, in order to ensure its exposition on the polymer coated magnetic nanoparticles (MNPs-FA). The prepared nanoparticles have been exhaustively characterized by different methods, including DLS, SEM, FT-IR and magnetic measurements. Magnetic nanoparticles showed dimensio…

IRON-OXIDE NANOPARTICLES; DRUG-DELIVERY; COPOLYMERSPolymersmedia_common.quotation_subjectBiomedical EngineeringPharmaceutical ScienceMedicine (miscellaneous)NanoparticleBioengineeringFolic AcidCoated Materials BiocompatibleCell Line TumorMaterials TestingHumansGeneral Materials ScienceViability assayMolecular Targeted TherapyInternalizationMagnetite Nanoparticlesmedia_commonChemistryNeoplasms Experimentalequipment and suppliesTreatment OutcomeTargeted drug deliveryCancer cellBiophysicsMCF-7 CellsMagnetic nanoparticlesNanocarriershuman activitiesFolate Targeting; Magnetic Nanoparticles; Cell Uptake; Ferrozine Assay; Polymer CoatingSuperparamagnetismJournal of biomedical nanotechnology
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Selective Uptake of Cylindrical Poly(2-Oxazoline) Brush-AntiDEC205 Antibody-OVA Antigen Conjugates into DEC-Positive Dendritic Cells and Subsequent T…

2014

To achieve specific cell targeting by various receptors for oligosaccharides or antibodies, a carrier must not be taken up by any of the very many different cells and needs functional groups prone to clean conjugation chemistry to derive well-defined structures with a high biological specificity. A polymeric nanocarrier is presented that consists of a cylindrical brush polymer with poly-2-oxazoline side chains carrying an azide functional group on each of the many side chain ends. After click conjugation of dye and an anti-DEC205 antibody to the periphery of the cylindrical brush polymer, antibody-mediated specific binding and uptake into DEC205(+) -positive mouse bone marrow-derived dendri…

ImmunoconjugatesOvalbuminPolymersT-LymphocytesT cellMolecular Sequence DataReceptors Cell SurfacePeptideLymphocyte ActivationCatalysisMinor Histocompatibility AntigensMicechemistry.chemical_compoundAntigenAntigens CDmedicineSide chainAnimalsLectins C-TypeAmino Acid SequenceReceptorOxazolesCells Culturedchemistry.chemical_classificationbiologyOrganic ChemistryDendritic CellsGeneral Chemistrymedicine.anatomical_structurechemistryBiochemistrybiology.proteinBiophysicsAzideAntibodyConjugateChemistry - A European Journal
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NQS-Doped PDMS Solid Sensor: From Water Matrix to Urine Enzymatic Application

2021

The development of in situ analytical devices has gained outstanding scientific interest. A solid sensing membrane composed of 1,2-naphthoquinone-4-sulfonate (NQS) derivatizing reagent embedded into a polymeric polydimethylsiloxane (PDMS) composite was proposed for in situ ammonium (NH4+) and urea (NH2CONH2) analysis in water and urine samples, respectively. Satisfactory strategies were also applied for urease-catalyzed hydrolysis of urea, either in solution or glass-supported urease immobilization. Using diffuse reflectance measurements combined with digital image processing of color intensity (RGB coordinates), qualitative and quantitative analyte detection was assessed after the colorime…

In situAnalyteMaterials scienceUreasePolymersClinical BiochemistrywaterNQS02 engineering and technologyureaurea hydrolysis01 natural sciencesArticlechemistry.chemical_compoundDimethylpolysiloxanesoptical sensorureaseglass supportChromatographyPolydimethylsiloxanebiology010405 organic chemistryGeneral Medicine021001 nanoscience & nanotechnologyurine0104 chemical sciencesin-situ analysisammoniumMembranechemistryReagentUreabiology.proteinColorimetry0210 nano-technologyTP248.13-248.65NaphthoquinonesNQS-PDMS sensorBiotechnologyBiosensors
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Kinetics of Anionic Living Copolymerization of Isoprene and Styrene Using in Situ NIR Spectroscopy: Temperature Effects on Monomer Sequence and Morph…

2019

The living anionic copolymerization of isoprene (I) and styrene (S) can afford a variety of different polymer microstructures that strongly depend on experimental parameters such as solvent, counte...

In situchemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryKineticsChemie02 engineering and technologyPolymer540010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciences0104 chemical sciencesStyreneInorganic ChemistrySolventchemistry.chemical_compoundMonomerchemistryMaterials ChemistryCopolymer0210 nano-technologyIsopreneMacromolecules
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Coordination polymer flexibility leads to polymorphism and enables a crystalline solid-vapour reaction: a multi-technique mechanistic study.

2015

Despite an absence of conventional porosity, the 1D coordination polymer [Ag4 (O2 C(CF2 )2 CF3 )4 (TMP)3 ] (1; TMP=tetramethylpyrazine) can absorb small alcohols from the vapour phase, which insert into AgO bonds to yield coordination polymers [Ag4 (O2 C(CF2 )2 CF3 )4 (TMP)3 (ROH)2 ] (1-ROH; R=Me, Et, iPr). The reactions are reversible single-crystal-to-single-crystal transformations. Vapour-solid equilibria have been examined by gas-phase IR spectroscopy (K=5.68(9)×10(-5) (MeOH), 9.5(3)×10(-6) (EtOH), 6.14(5)×10(-5) (iPrOH) at 295 K, 1 bar). Thermal analyses (TGA, DSC) have enabled quantitative comparison of two-step reactions 1-ROH→1→2, in which 2 is the 2D coordination polymer [Ag4 (O2 …

In situporosityin situ diffractionCoordination polymerStereochemistrygas-phase spectroscopyInfrared spectroscopyCatalysislaw.inventionpolymorphismchemistry.chemical_compoundOptical microscopelawQDThermal analysisTP155chemistry.chemical_classificationChemistryOrganic ChemistryGeneral ChemistryPolymerCoordination PolymersFull PapersCrystallographyPolymorphism (materials science)microscopysolid-state reactionsPowder diffractionthermal analysisChemistry (Weinheim an der Bergstrasse, Germany)
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