Search results for " polymerization"

showing 10 items of 1054 documents

Mechanism of anionic polymerization of (meth)acrylates in the presence of aluminium alkyls, 1. 13C NMR studies of model compounds in toluene

1994

The bimetallic ate complex [(CH 3 ) 2 C=C(OEt)(O - AlR 3 )]Li + is regarded to be the model of the active centre of the polymerization of methyl methacrylate in the presence of aluminium alkyls. This complex is detectable by 13 C NMR up to 273 K. At ambient temperature irreversible decomposition takes place. Apart from the formation of the ate complex, excess aluminium chloride coordinates to the ester carbonyl groups of both the monomer and the polymer chain

Aluminium chloridePolymers and PlasticsOrganic Chemistrychemistry.chemical_elementCarbon-13 NMRAte complexchemistry.chemical_compoundMonomerAnionic addition polymerizationchemistryPolymerizationAluminiumPolymer chemistryMaterials ChemistrymedicineMethyl methacrylatemedicine.drugMacromolecular Rapid Communications
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On the formation of inclusion complexes at the solid/liquid interface of anchored temperature-responsive PNIPAAM diblock copolymers with γ-cyclodextr…

2017

The thermal responsive behavior of adsorbed layers of diblock copolymers of poly(N-isopropylacrylamide) (PNIPAAM) and poly((3-acrylamidopropyl)trimethylammonium chloride) (PAMPTMA(+)) with γ-cyclodextrin (γ-CD) at the solid/liquid interface has been investigated using three in situ techniques: null ellipsometry, quartz–crystal microbalance with dissipation monitoring, and neutron reflectometry. The measurements provided information about the adsorbed amounts, the layer thickness, hydration and viscoelastic properties, and the interfacial structure and composition. The copolymers adsorb to silica with the cationic PAMPTMA(+) blocks sitting as anchors in a flat conformation and the PNIPAAM ch…

AmidePolymers and PlasticsBlock copolymerReflectometerReflection02 engineering and technology01 natural sciencessupramolecular chemistryquartz crystal microbalancechemistry.chemical_compoundColloid and Surface ChemistryEllipsometryViscoelasticity Inclusion complexCopolymerMaterials ChemistryPoly (n isopropylacrylamide)Poly(N-isopropylacrylamide)Settore CHIM/02 - Chimica Fisicachemistry.chemical_classification/dk/atira/pure/subjectarea/asjc/1600/1606Reflectometry/dk/atira/pure/subjectarea/asjc/1500/1505Cyclodextrinunclassified drug Article021001 nanoscience & nanotechnologyThermoresponsive block copolymerpriority journalsolidpolymerizationPoly(N-isopropylacrylamide)synthesiNeutron reflectometrypolyrotaxane0210 nano-technologyellipsometryMaterials science/dk/atira/pure/subjectarea/asjc/2500/2505/dk/atira/pure/subjectarea/asjc/2500/2507poly(n isopropylacrylamide)010402 general chemistryLower critical solution temperatureAcrylic monomeratom transfer radical polymerizationAdsorptioncomplex formationPolymer chemistryCyclodextrinliquidPhysical and Theoretical ChemistrySolid/liquid interfaceThermo-responsive Hydrogels copolymerneutron reflectometryInclusion complexgamma cyclodextrinCationic polymerization0104 chemical sciencessolid liquid interfacechemistryChemical engineeringInvited ArticleColloid and Polymer Science
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Cationic amino acid transport across the blood-brain barrier is mediated exclusively by system y+.

2006

Cationic amino acid (CAA) transport is brought about by two families of proteins that are found in various tissues: Cat (CAA transporter), referred to as system y+, and Bat [broad-scope amino acid (AA) transporter], which comprises systems b0,+, B0,+, and y+L. CAA traverse the blood-brain barrier (BBB), but experiments done in vivo have only been able to examine the BBB from the luminal (blood-facing) side. In the present study, plasma membranes isolated from bovine brain microvessels were used to identify and characterize the CAA transporter(s) on both sides of the BBB. From these studies, it was concluded that system y+was the only transporter present, with a prevalence of activity on the…

Amino Acid Transport System y+PhysiologyStereochemistryPolarity (physics)Endocrinology Diabetes and MetabolismBiological Transport ActiveBiologyBlood–brain barrierNitric OxidePhysiology (medical)CationsmedicineAnimalsAmino AcidsCells Culturedchemistry.chemical_classificationCationic polymerizationEndothelial CellsTransporterAmino acidmedicine.anatomical_structureBiochemistrychemistryBlood-Brain BarrierAmino Acid Transport Systems BasicCattleNitric Oxide SynthaseAmerican journal of physiology. Endocrinology and metabolism
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Surfactant effect on the physicochemical characteristics of cationic solid lipid nanoparticles

2016

Solid lipid nanoparticles (SLNs) may be considered as a new approach for therapeutics for many diseases. In addition to drug delivery, their use as non-viral vectors for gene delivery can be obtained by including cationic lipids, which provide a positive surface potential that favors binding to the nucleic acids as DNA, siRNA, miRNA, etc. In fact, the addition of cationic surfactants is indispensable for obtaining nanoparticles with surface positive charge. In this study, three different cationic lipids (dioctadecyl dimethyl ammonium bromide, cetyltrimethyl ammonium bromide, cetylpyridinium chloride) and Brij 76 as nonionic surfactant were employed to formulate Precirol ATO 5 based cSLN usi…

Ammonium bromideBiocompatibilitysurfactantGreen Fluorescent ProteinsPharmaceutical ScienceCetylpyridinium02 engineering and technologyGene deliveryCationic solid lipid nanoparticleCetylpyridinium chloridePolyethylene GlycolsDiglyceridesSurface-Active Agents03 medical and health scienceschemistry.chemical_compound0302 clinical medicinePulmonary surfactantCationsSolid lipid nanoparticleHumansOrganic chemistrycharacterizationGene deliveryLuciferasesnanocarriersCetrimoniumGene Transfer TechniquesCationic polymerizationDNAGenetic Therapy021001 nanoscience & nanotechnologyLipidsCombinatorial chemistryQuaternary Ammonium Compoundschemistrygene delivery.Settore CHIM/09 - Farmaceutico Tecnologico Applicativo030220 oncology & carcinogenesisNanocarrierDrug deliveryCetrimonium CompoundsNanoparticles0210 nano-technologycationic solid lipid nanoparticlesPlasmids
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Tuning the selectivity of molecularly imprinted polymer extraction of arylcyclohexylamines: From class-selective to specific

2020

Abstract A molecularly imprinted polymer (MIP) has been prepared in presence of 3-hydroxy phencyclidine (3-OH PCP) as template by bulk polymerization using N,N-dimethylformamide, as porogenic solvent, for the selective solid-phase extraction (SPE) of arylcyclohexylamines from oral fluids. Experimental variables of the extraction procedure have been studied in order to increase both, extraction recovery of 3-OH PCP, used as model analyte, and imprinting factor. By modifying the composition of the washing solvent, the selectivity of the MIP extraction procedure can be tuned, moving from an arylcyclohexylamine selective method to a 3-OH PCP specific method. The applicability of the synthesized…

AnalyteArylcyclohexylamineBulk polymerizationSurface PropertiesIon-mobility spectrometry02 engineering and technology01 natural sciencesBiochemistryPolymerizationAnalytical ChemistryMolecularly Imprinted PolymersIon Mobility SpectrometrymedicineEnvironmental ChemistryParticle SizeSpectroscopyDetection limitCyclohexylaminesChromatographyMolecular StructureChemistry010401 analytical chemistryMolecularly imprinted polymer021001 nanoscience & nanotechnology0104 chemical sciencesSolvent0210 nano-technologySelectivitymedicine.drugAnalytica Chimica Acta
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Analysis of basic drugs by liquid chromatography with environmentally friendly mobile phases in pharmaceutical formulations

2017

Abstract Basic drugs are positively charged in the usual working pH (2–8) in reversed-phase liquid chromatography. This gives rise to a strong association with the residual ionized silanols in conventional silica-based stationary phases, which is translated in poor peak shape and high consumption of organic solvent to get appropriate retention times. Micellar mobile phases containing surfactants give rise to modified stationary phases, where silanols are masked, improving the peak shape. However, mobile phases containing the anionic surfactant sodium dodecyl sulfate (SDS) require a small amount of organic solvent to conveniently decrease the retention of cationic analytes. An alternative is…

AnalyteMethod validation01 natural sciencesAnalytical Chemistrylaw.inventionchemistry.chemical_compoundPulmonary surfactantlawmedicineSample preparationSodium dodecyl sulfateBrij-35β-Adrenoceptor antagonistsSodium dodecyl sulfateSpectroscopyFiltrationChromatography010405 organic chemistryChemistry010401 analytical chemistryCationic polymerizationEnvironmentally friendly0104 chemical sciencesOxprenololPharmaceutical formulationsmedicine.drug
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Polyacrylonitrile block copolymers for the preparation of a thin carbon coating around TiO2 nanorods for advanced lithium-ion batteries.

2013

Herein, a new method for the realization of a thin and homogenous carbonaceous particle coating, made by carbonizing RAFT polymerization derived block copolymers anchored on anatase TiO2 nanorods, is presented. These block copolymers consist of a short anchor block (based on dopamine) and a long, easily graphitizable block of polyacrylonitrile. The grafting of such block copolymers to TiO2 nanorods creates a polymer shell, which can be visualized by atomic force microscopy (AFM). Thermal treatment at 700 °C converts the polyacrylonitrile block to partially graphitic structures (as determined by Raman spectroscopy), establishing a thin carbon coating (as determined by transmission electron m…

AnataseMaterials sciencePolymers and PlasticsSurface PropertiesAcrylic Resins02 engineering and technologyThermal treatmentLithium010402 general chemistry01 natural scienceschemistry.chemical_compoundElectric Power SuppliesMaterials ChemistryCopolymerReversible addition−fragmentation chain-transfer polymerizationComposite materialParticle Sizechemistry.chemical_classificationIonsTitaniumNanotubesMolecular StructureOrganic ChemistryPolyacrylonitrileTemperaturePolymerElectrochemical Techniques021001 nanoscience & nanotechnologyCarbon0104 chemical scienceschemistryTransmission electron microscopyNanorod0210 nano-technologyMacromolecular rapid communications
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Stabilizing nanostructured lithium insertion materials via organic hybridization: A step forward towards high-power batteries

2014

Abstract Herein, we present the electrochemical characterization of carbon-coated TiO 2 nanorods, obtained by carbonizing RAFT (reversible addition fragmentation chain transfer) polymerization derived block copolymers anchored on anatase TiO 2 nanorods. These carbon-coated TiO 2 nanorods show an improved electrochemical performance in terms of first cycle reversibility, specific capacity, cycling stability, and high rate capability. More importantly, however, the structural disordering observed in the uncoated TiO 2 nanorods by means of galvanostatic and potentiodynamic cycling as well as ex situ XRD analysis, does not occur for the carbon-coated material. Preventing this structural disorde…

AnataseMaterials scienceRenewable Energy Sustainability and the EnvironmentInorganic chemistryEnergy Engineering and Power Technologychemistry.chemical_elementChain transferElectrochemistryPolymerizationchemistryCopolymerReversible addition−fragmentation chain-transfer polymerizationLithiumNanorodElectrical and Electronic EngineeringPhysical and Theoretical ChemistryJournal of Power Sources
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Polymerization with heterogeneous metalorganic catalysts. VI. Differences in polymerization activity of α-olefins and some kinetic results on butene-…

1967

Relative changes in polymerization activity of ethylene, propylene, and butene-1 in Ziegler-Natta polymerization were compared by use of TiCl3 samples contaminated with O2 and H2O to various extents. Catalyst depletion varied for the three monomers which supported the existence of different active centers. In butene-1 polymerizations with the system Al(C2H5)2Cl–TiCl3, the formation of active centers involves an irreversible and a reversible (adsorption) reaction, the former pertaining to the formation of Al(C2H5)Cl2 and dependent upon the purity of the TiCl3. The kinetic treatment of the rate curves suggests a mixed order of catalyst deactivation and again points to the importance of Al(C2H…

Anionic addition polymerizationChain-growth polymerizationBulk polymerizationPolymerizationChemistryPolymer chemistryGeneral EngineeringCationic polymerizationPrecipitation polymerizationCoordination polymerizationPhotochemistryIonic polymerizationJournal of Polymer Science Part A-1: Polymer Chemistry
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Some New Copolymers by Ionic Polymerization

1980

In the first part the cationic polymerization of a homologous series of cyclic ether–acetals with ring sizes of 11, 14, and 17 atoms is described. During the polymerization of triethylene glycol formal (TGF) an equilibrium is reached and besides high polymers cyclic oligomers are formed. The oligomers and the polymers are built up of a regular sequence of one oxymethylene unit and three oxyethylene units –[–(OCH2) (OC2H4)3–]–x. They are therefore be labelled a “sequenced copolymer.” The equilibrium concentrations of the cyclic oligomers with a polymerization degree from 2 to 15 follow the Jacobson–Stockmayer equation. The 14- and 17-membered monomers POC and HOC forms cyclic oligomers and h…

Anionic addition polymerizationChain-growth polymerizationPolymers and PlasticsPolymerizationChemistryPolymer chemistryMaterials ChemistryCationic polymerizationCopolymerLiving polymerizationIonic polymerizationRing-opening polymerizationPolymer Journal
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