Search results for "polymers"

showing 10 items of 3567 documents

Structure of Polymer Brushes in Cylindrical Tubes: A Molecular Dynamics Simulation

2006

Molecular Dynamics simulations of a coarse-grained bead-spring model of flexible macromolecules tethered with one end to the surface of a cylindrical pore are presented. Chain length $N$ and grafting density $\sigma$ are varied over a wide range and the crossover from ``mushroom'' to ``brush'' behavior is studied for three pore diameters. The monomer density profile and the distribution of the free chain ends are computed and compared to the corresponding model of polymer brushes at flat substrates. It is found that there exists a regime of $N$ and $\sigma$ for large enough pore diameter where the brush height in the pore exceeds the brush height on the flat substrate, while for large enoug…

Polymers and PlasticsFOS: Physical sciencesSubstrate (electronics)Condensed Matter - Soft Condensed MatterInorganic ChemistryQuantitative Biology::Subcellular Processeschemistry.chemical_compoundColloidMolecular dynamicsPolymer chemistryMaterials Chemistrychemistry.chemical_classificationPhysics::Biological PhysicsQuantitative Biology::BiomoleculesOrganic ChemistryPolymerCondensed Matter PhysicsCondensed Matter::Soft Condensed MatterMonomerComputer Science::GraphicschemistryChemical physicsExcluded volumeSoft Condensed Matter (cond-mat.soft)Layer (electronics)Macromolecule
researchProduct

Maleimide Glycidyl Ether: A Bifunctional Monomer for Orthogonal Cationic and Radical Polymerizations.

2015

A novel bifunctional monomer, namely maleimide glycidyl ether (MalGE), prepared in a four-step reaction sequence is introduced. This monomer allows for selective (co)polymerization of the epoxide group via cationic ring-opening polymerization, preserving the maleimide functionality. On the other hand, the maleimide functionality can be copolymerized via radical techniques, preserving the epoxide moiety. Cationic ring-opening multibranching copolymerization of MalGE with glycidol was performed, and a MalGE content of up to 24 mol% could be incorporated into the hyperbranched polymer backbone (Mn = 1000-3000 g mol(-1)). Preservation of the maleimide functionality during cationic copolymerizat…

Polymers and PlasticsFree RadicalsChemistryPolymersPropanolsOrganic ChemistryRadical polymerizationCationic polymerizationChain transferPolymerizationMaleimideschemistry.chemical_compoundPolymerizationCationsMaterials ChemistryCopolymerOrganic chemistryEpoxy CompoundsReversible addition−fragmentation chain-transfer polymerizationIonic polymerizationMaleimideEthersMacromolecular rapid communications
researchProduct

Single-Crystal-to-Single-Crystal Anion Exchange in a Gadolinium MOF: Incorporation of POMs and [AuCl4]−

2016

The encapsulation of functional molecules inside porous coordination polymers (also known as metal-organic frameworks, MOFs) has become of great interest in recent years at the field of multifunctional materials. In this article, we present a study of the effects of size and charge in the anion exchange process of a Gd based MOF, involving molecular species like polyoxometalates (POMs), and [AuCl4]−. This post-synthetic modification has been characterized by IR, EDAX, and single crystal diffraction, which have provided unequivocal evidence of the location of the anion molecules in the framework.

Polymers and PlasticsGadoliniumInorganic chemistryPorous Coordination Polymerschemistry.chemical_element010402 general chemistry01 natural sciencesArticleSingle Crystal DiffractionIonlcsh:QD241-441lcsh:Organic chemistryFunctional importanceanion exchangeMoleculepolyoxometalatesMaterialsIon exchange010405 organic chemistryGeneral ChemistryMOFs; anion exchange; polyoxometalatesMOFs0104 chemical sciencesCrystallographychemistryCristallsCompostos de coordinacióSingle crystalPolymers
researchProduct

Modification of carboxyl groups of poly(ethylene-co-acrylic acid) via facile wet chemistry method: A kinetic study

2010

Abstract In this work, we present the results of a kinetic study of the surface modification of the carboxyl group of poly(ethylene-co-acrylic acid) into acyl chloride. Reaction temperature and time, concentration of the reactants, kind of agitation have been changed in order to understand their effect on the conversion. A study on the penetration of the reaction inside the sample bulk was also performed. The results indicate that, when short reaction times are adopted, the reaction limits to the outer layers of the samples and, in this case, on increasing the temperature, the concentration of the reactants and the stirring allows having a faster kinetic. At longer reaction times, the react…

Polymers and PlasticsGeneral Chemical EngineeringChemical modificationGeneral ChemistryPenetration (firestop)BiochemistryContact anglechemistry.chemical_compoundPoly(ethylene-co-acrylic acid)Surface modificationSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryAcyl chlorideChemical engineeringPolymer chemistryMaterials ChemistryEnvironmental ChemistrySurface modificationFourier transform infrared spectroscopyFunctionalizationWet chemistryAcrylic acid
researchProduct

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
researchProduct

Water sorption isotherms of molecularly imprinted polymers. Relation between water binding and iprodione binding capacity

2017

International audience; Molecularly imprinted polymers are often used in aqueous medium in order to recognize specifically a target molecule. The molecular recognition is usually based on hydrogen bonding. In this case, water molecule presents a serious competition towards the target molecule. In this study, the water sorption by molecularly imprinted polymers was studied in aqueous medium. The molecularly imprinted polymers were specific for iprodione fungicide and were prepared using a 24 full factorial experimental design. They were synthesized using EGDMA or TRIM as crosslinker, methacrylamide or styrene as functional monomer and using bulk or precipitation polymerization. The water sor…

Polymers and PlasticsGeneral Chemical EngineeringIprodione02 engineering and technologyGAB model01 natural sciencesBiochemistryStyrenechemistry.chemical_compound[SDV.IDA]Life Sciences [q-bio]/Food engineeringMaterials ChemistryEnvironmental ChemistryMoleculeOrganic chemistryMethacrylamidechemistry.chemical_classificationHydrogen bond010401 analytical chemistryMolecularly imprinted polymer[ SDV.IDA ] Life Sciences [q-bio]/Food engineeringGeneral ChemistryPolymerPeleg's model021001 nanoscience & nanotechnology0104 chemical scienceschemistryChemical engineeringMolecularly imprinted polymersWater sorptionPrecipitation polymerization0210 nano-technologyWater binding
researchProduct

Pulsatile protein release and protection using radiation-crosslinked polypeptide hydrogel delivery devices

2011

Abstract In the recent years recombinant technology has identified numerous protein based therapeutics. Their effective delivery, though, can be challenging due to the poor stability of most proteins along their pathway to the target site in the body. Hydrogels have been identified as good candidates for protein encapsulation and delivery thanks to both material and manufacturing process advantages. In this work we propose high energy irradiation as a synthetic methodology of choice to engineer hydrogel-based delivery devices for encapsulation and pulsatile release of proteins, triggered by pH, and for prevention of their denaturation when encapsulated. In particular, maleic anhydride funct…

Polymers and PlasticsGeneral Chemical EngineeringKineticsMechanical propertiesPolyaspartamide High energy irradiationBiochemistryViscoelasticitychemistry.chemical_compoundPolymer chemistryMaterials ChemistrymedicineEnvironmental ChemistryProtein releasetechnology industry and agricultureMaleic anhydrideGeneral ChemistryPolyaspartamidechemistryChemical engineeringRubber elasticitySelf-healing hydrogelsLiberationpH-responsive hydrogelsSettore CHIM/07 - Fondamenti Chimici Delle TecnologieSwellingmedicine.symptompH-responsive hydrogelDrug carrierMechanical propertieHigh energy irradiation
researchProduct

Optimization of synthesis of a titaniumcatalyst supported on alumina for synthesis of ultra-high molecular-weightpolyethylene (UHMWPE)

1994

Ethylene polymerized under low pressure over a catalytic system (modified Аl2Оз/ТlСl4 + AlEt2Cl) yields UHMWPE. Alumina gel chlorinated and calcined (above 773 K) was used as a catalyst carrier. The effect of the main variables of carrier chlorination (concentration of HCl, chlorination time and temperature) and of the calcination temperature on activity of the catalytic system was investigated. A mathematical method of planning experiments and evaluating experimental results was used in order to improve both the analysis of the conditions of the preliminary modification of the support and their optimization. Relationships between the surface properties of the alumina carrier and the activi…

Polymers and PlasticsGeneral Chemical EngineeringMaterials ChemistryPolimery
researchProduct

Investigation of polymer organic deposit formed on nickel phosphate in oxidative dehydrogenation of ethylbenzene

1997

Abstract Several polymer organic deposits (PODS) had been obtained by heating of nickel polyphosphate (NiP) at 720 K for 1, 4, or 10 h in a stream of helium (carrier gas) containing 20% of (ethylbenzene : oxygen= 1: 0.5] mixture. The samples were tested in oxidative dehydrogenation (OD) of ethylbenzene (EB) to styrene, before and after their separation from the inorganic part of NiP as catalysts. Some functional groups or bonds, important for enhancement of styrene yield, have been found in the PODS. The POD obtained after 10-h coking of NiP, containing a mixture of both insoluble fused-ring and soluble-in-pyridine macromolecules, provided with at least two types of catalytically active cen…

Polymers and PlasticsGeneral Chemical EngineeringPolyphosphateInorganic chemistrychemistry.chemical_elementGeneral ChemistryBiochemistryEthylbenzeneStyreneCatalysisActive centerchemistry.chemical_compoundNickelchemistryMaterials ChemistryEnvironmental ChemistryNIPDehydrogenationReactive and Functional Polymers
researchProduct

Polymerizable ring-shaped molecules containing aspartic acid: synthesis and free radical polymerization of a macrocycle derived from (N'-methacryloyl…

1999

A novel polymerizable macrocycle, 6, was prepared using high dilution techniques. Starting from N-(N'-methacryloyl-11-aminoundecanoyl)-L-aspartic acid dimethyl ester (2), N-(N'methacryloyl-11-aminoundecanoyl)-α,β-bis( 4,9-dioxadodecane-1,12-diamine)-L-aspartic acid amide (4) was obtained via amino-lysis with the bifunctional amine 4,9-dioxadodecane-1,12-diamine (3) in high excess. Addition of the free amino groups to toluene-2,4-diisocyanate (5) under high dilution provided macrocycle 6. The existence and purity of 6 were confirmed by mass spectrometry, NMR and IR spectroscopy, and HPLC. The methacrylic function was used to build up oligomers by free radical polymerization, using AIBN as an…

Polymers and PlasticsGeneral Chemical EngineeringRadical polymerizationGeneral ChemistryToluenechemistry.chemical_compoundLiving free-radical polymerizationEnd-groupchemistryPolymerizationDiamineAmidePolymer chemistryMaterials ChemistryOrganic chemistryBifunctionalDesigned Monomers and Polymers
researchProduct