Search results for "Polymerization"

showing 10 items of 1689 documents

Copolymerization of vinylidene fluoride and acrylic acid in supercritical carbon dioxide

2009

The free-radical copolymerization of vinylidene fluoride (VDF) and acrylic acid (AA) was carried out in supercritical carbon dioxide using both precipitation and dispersion techniques in the presence of an ammonium carboxylate perfluoropolyether compound. Formation of a copolymer was confirmed by variable contact time CP MAS NMR spectroscopy. Macromolecular matrices were significantly enriched in AA with respect to the initial feed composition and we found that the nonfluorinated monomer has a much higher reactivity ratio with respect to VDF. The cumulative concentration, crystallinity, and water affinity of the synthesized copolymers could be modified changing the initial feed composition,…

Dispersion polymerizationSupercritical carbon dioxidePolymers and PlasticsOrganic ChemistryRadical polymerizationSupercritical fluidchemistry.chemical_compoundMonomerchemistryPolymerizationChemical engineeringPolymer chemistryMaterials ChemistryCopolymerAcrylic acidJournal of Polymer Science Part A: Polymer Chemistry
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Copolymerization of VDF and HFP in Supercritical Carbon Dioxide: Experimental Analysis of the Reaction Loci

2010

Free radical copolymerization reactions of vinylidene fluoride (VDF) and hexafluoropropylene (HFP) were carried out in supercritical carbon dioxide at T=50 °C. When ammonium carboxylate perfluoropolyether surfactants were used, the formation of polymer particles was observed provided that HFP mole fraction in the feed was not larger than 0.30. Under these conditions, the effect of the total interphase area of the polymer phase, Ap, on the product propertieswas investigated by comparing experiments with largely different amounts of stabilizer, i.e., ranging from precipitation (smaller Ap) to dispersion (larger Ap) polymerization systems. We found that the copolymer molecular weight distribut…

Dispersion polymerizationSupercritical carbon dioxidePolymers and PlasticsOrganic ChemistryRadical polymerizationsupercritical carbon dioxide fluoropolymers free radical polymerization polymerization kineticsSettore ING-IND/27 - Chimica Industriale E TecnologicaInorganic Chemistrychemistry.chemical_compoundchemistryPolymer chemistryCarbon dioxideMaterials ChemistryCopolymerCarboxylateHexafluoropropyleneFluoride
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Dispersion polymerization of vinyl monomers in supercritical carbon dioxide in the presence of drug molecules: A one-pot route for the preparation of…

2008

The polymerization of 1-vinyl-2-pyrrolidone in supercritical carbon di- oxide in the presence of ibuprofen as a model drug was investigated as a new one-pot process for the preparation of polymer-based drug delivery systems (DDSs). The com- posites were prepared at 65 � C and P ¼ 31-42 MPa by changing the initial con- centration of the drug and the concentration of a crosslinking agent and that of a hydrophobic comonomer. The effects of these parameters on the performances of the polymerization and on the in vitro release kinetics of ibuprofen were studied. In all the experiments, part of the drug was entrapped inside the polymer particles and dissolved more slowly with respect to the pure …

Dispersion polymerizationSupercritical carbon dioxidePolymers and PlasticsOrganic ChemistryRadical polymerizationtechnology industry and agriculturemacromolecular substanceschemistry.chemical_compoundMonomerchemistryPolymerizationDrug deliveryPolymer chemistryMaterials ChemistryCopolymerDrug carrierJournal of Polymer Science Part A: Polymer Chemistry
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Liquid-Crystalline Colloidal Particles

2004

Here we report about the synthesis of colloidal particles of nematic and smectic liquid-crystalline polymers. For this purpose mesogen-containing acrylate monomers were synthesized and polymerized in a special modification of a precipitation polymerization called dispection polymerization. By variation of the polymerization conditions colloidal particles of different size and polydispersity could be obtained including very narrowly distributed samples in optimized batches. On azobenzene-containing colloidal particles switching experiments with polarized light were performed. It could be observed that the nematic director of the mesogens within the colloidal particles can be rotated due to t…

Dispersion polymerizationchemistry.chemical_classificationAcrylate polymerMaterials sciencePolymers and Plasticsdigestive oral and skin physiologyOrganic ChemistryRadical polymerizationDispersityPolymerCondensed Matter Physicschemistry.chemical_compoundchemistryPolymerizationPolymer chemistryMaterials ChemistryPrecipitation polymerizationParticle sizePhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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Control of mesogen configuration in colloids of liquid crystalline polymers

2010

We report on a method to chemically predetermine the surface anchoring of mesogens in liquid crystalline colloids formed by different types of dispersion polymerization, and hence to achieve control over the mesogen configuration in such colloids. The surface anchoring is controlled by the chemical linkage of the polymers forming the colloids to the surfactants stabilizing the colloids towards the dispergent. We find that the hydroxypropyl cellulose used in conventional dispersion poylmerization induces parallel mesogen surface anchoring that in turn leads to bipolar director-field configurations, while a methacrylate terminated polysiloxane stabilizer, which is used in nonpolar dispersion …

Dispersion polymerizationchemistry.chemical_classificationMaterials scienceHydroxypropyl celluloseMesogenGeneral ChemistryPolymerCondensed Matter PhysicsMethacrylatechemistry.chemical_compoundColloidchemistryChemical engineeringPolymer chemistryCopolymerDispersion (chemistry)Soft Matter
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Polymerization of methyl methacrylate through ionizing radiation in CO2-based dense systems

2000

Herein, we report the use of ionizing radiation to induce a dispersion polymerization reaction in dense CO2. As a model system, the polymerization of methyl methacrylate in the presence of poly(dimethylsiloxane) stabilizers was investigated. It was demonstrated that the dose plays the key role in the progress of the reaction and in the morphology of the resulting polymer. Dispersion polymerization carried out in the presence of mono- and bifunctionalized surfactants gave differently structured polymers. The polymers obtained have been characterized by scanning electron microscopy, solubility tests, and gel permeation chromatography, and the molecular structure has been related to dynamic me…

Dispersion polymerizationchemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryPolymerInorganic ChemistryGel permeation chromatographychemistry.chemical_compoundChain-growth polymerizationchemistryPolymerizationChemical engineeringPolymer chemistrySupercritical fluids polymersMaterials ChemistrySolubilityMethyl methacrylateIonic polymerization
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Polymer Synthesis in Supercritical Carbon Dioxide

2003

It is current opinion of most of the people involved in supercritical fluids (SCFs) technology that as the end of the twentieth century has been devoted to enlarge exploitation of compressed gases in separation processes the beginning of the twenty-first will be mainly aimed to improve their utilisation as solvents for reactions.

Dispersion polymerizationchemistry.chemical_classificationchemistry.chemical_compoundSupercritical water oxidationMaterials scienceSupercritical carbon dioxidechemistryChemical engineeringVinyl acetatePolymerCurrent (fluid)Supercritical fluidElectrochemical reduction of carbon dioxide
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Synthesis of Liquid-Crystalline Colloids in Nonpolar Media and their Manipulation in Electric Fields

2009

The first synthesis of anisotropic liquid-crystalline colloids in silicone oil by a direct (radical) polymerization of a monomer in THF/silicone oil mixtures with the help of siloxane containing stabilizers is described. The size of the colloids is in the lower μm range and can be adjusted by varying the mixture. The resulting colloids show a bipolar director configuration if they are small (<1.5 μm) and a radial configuration if they are larger. The colloids are sterically stabilized, and, due to the nonpolarity of the solvent, the disturbing effects of migrating ions are excluded and experiments in the electric field can be conducted. Both line formation in DC fields and a periodic switch…

Dispersion polymerizationendocrine systemPolymers and PlasticsChemistrydigestive oral and skin physiologyOrganic ChemistryRadical polymerizationCondensed Matter Physicscomplex mixturesSilicone oilColloidchemistry.chemical_compoundPolymerizationSiloxaneElectric fieldPolymer chemistryMaterials ChemistryParticle sizePhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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Zur kinetik der anionischen polymerisation von methyl-methyacrylat in tetrahydrofuran bei −75°C

1973

Die anionische Polymerisation von Methylmethacrylat (MMA) in Tetrahydrofuran (THF) verlauft bei −75°C mit Cumylcasium bzw. oligomerem α-Methylstyrylcasium als Initiatoren ohne erkennbare Nebenreaktionen analog der anionischen Polymerisation von unpolaren Monomeren in atherischen Losungsmitteln. Als Beweis wird hauptsachlich die enge Molekulargewichtsverteilung der unter diesen Bedingungen hergestellten Polymethylmethacrylate angefuhrt. Bei −75°C betragen die Geschwindigkeitskonstanten fur die Monomeranlagerung an das Ionenpaar kw(±) = 80 dm3 mol−1 s−1 und an das freie Anion etwa kw(−) ≈ 6 · 104 dm3 mol−1 s−1. Leitfahigkeitsmessungen ergeben, das die Dissoziationskonstante des Polymethylmeth…

Dissociation constantchemistry.chemical_compoundMonomerAnionic addition polymerizationReaction rate constantchemistryPolymerizationPolymer chemistryMolar mass distributionTetrahydrofuranDie Makromolekulare Chemie
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Cationic Supramolecular Vesicular Aggregates for Pulmonary Tissue Selective Delivery in Anticancer Therapy

2016

The biopharmaceutical properties of supramolecular vesicular aggregates (SVAs) were characterized with regard to their physicochemical features and compared with cationic liposomes (CLs). Neutral and cationic SVAs were synthesized using two different copolymers of poly(aspartyl hydrazide) by thin-layer evaporation and extrusion techniques. Both copolymers were self-assembled in pre-formulated liposomes and formed neutral and cationic SVAs. Gemcitabine hydrochloride (GEM) was used as an anticancer drug and loaded by a pH gradient remote loading procedure, which significantly increased drug loading inside the SVAs. The resulting average size of the SVAs was 100 nm. The anticancer activity of …

DrugBiodistributionMacromolecular Substancesmedia_common.quotation_subjectSupramolecular chemistryAntineoplastic Agents02 engineering and technology010402 general chemistryHydrazideDeoxycytidine01 natural sciencesBiochemistryGemcitabine Hydrochloridesupramolecular chemistryStructure-Activity Relationshipchemistry.chemical_compoundDrug Delivery SystemsCationsDrug DiscoveryTumor Cells CulturedAnimalsHumansTissue DistributionCationic liposomeRats WistarGeneral Pharmacology Toxicology and Pharmaceuticsvesicular aggregatesCell Proliferationmedia_commonPharmacologyLiposomeDose-Response Relationship DrugMolecular StructurenanoparticleOrganic ChemistryCationic polymerization021001 nanoscience & nanotechnologyGemcitabineRats0104 chemical scienceschemistryBiochemistryantitumor agentliposomeMolecular MedicineDrug Screening Assays Antitumor0210 nano-technologyChemMedChem
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