Search results for "polymerization"

showing 10 items of 1689 documents

Room temperature ionic liquids based on cationic porphyrin derivatives and tetrakis(pentafluorophenyl)borate anion

2011

A series of 11 low melting ionic liquids based on meso-substituted A3B -porphyrins and A2B2-porphyrins containing one or two pyridyl substituents have been synthesized in high yields. Three of them are liquids at room temperature. All these porphyrinic salts were characterized by1H NMR,19F NMR, MALDI-TOF mass spectrometry, elemental analysis and UV-visible spectroscopy. The thermal properties and conductivity values of these salt derivatives have been also measured. A specific conductivity value of up to 4 mS.cm-1could be obtained for a compound having the counter-anion B(C6F5)4-.

A(2)B(2)-porphyrinsMediaInorganic chemistrySalt (chemistry)tetrakis(pentafluorophenyl)borate anionExtractionConductivityElectrochemistryCatalysisIonDscchemistry.chemical_compoundElectrolyteElectrochemistryMolten-Saltschemistry.chemical_classificationTgaCationic polymerizationGeneral ChemistryA(3)B-porphyrinsPorphyrinRT ionic liquidschemistrySensitized Solar-CellsIonic liquidProton NMRconductivity
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Hybrid layers of etch-and-rinse versus self-etching adhesive systems.

2010

Objective: To evaluate the effectiveness in the formation of resin tags, adhesive lateral branches and hybrid layers of five adhesive systems, when bonding to dentine. Material and Methods: Flat dentin surfaces from 25 molars were bonded with several adhesive systems according to the manufacturers? instructions. Composite build-ups were constructed incrementally with Tetric Ceram. The Specimens were sectioned parallel to the long axis. One section was treated with phosphoric acid and sodium hypochlorite in order to reveal the hybrid layer formation. The other section was stored in 30% hydrochloric acid to detect resin tags and adhesive lateral branch formation. Results: The two etch-and-rin…

Absorption of waterMaterials scienceScanning electron microscopeComposite numberDental Cementschemistry.chemical_compoundstomatognathic systemDentinmedicineHumansComposite materialGeneral DentistryBondingtechnology industry and agricultureDental Bonding:CIENCIAS MÉDICAS [UNESCO]medicine.anatomical_structureOtorhinolaryngologyPolymerizationchemistrySodium hypochloriteUNESCO::CIENCIAS MÉDICASDentinDental EtchingMicroscopy Electron ScanningSurgeryAdhesiveScanning electron microscopyLayer (electronics)Bonding Dentin Scanning electron microscopy
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Reversible isomerization of metal nanoclusters induced by intermolecular interaction

2021

Most inorganic nanoparticles are directly surface-terminated (and -stabilized) by protecting ligands, which could greatly affect the atomic packing and physical/chemical properties of their inorganic cores. Here, we show that the intermolecular interactions between the adsorbed molecules and surface ligands can also affect the core structure of inorganic nanoparticles. Through the coupling/decoupling of cationic surfactants (cetyltrimethylammonium cations, CTA+) and anionic surface ligands (para-mercaptobenzoic acid, p-MBA) in the aqueous phase, we have achieved a reversible transformation between two isomers of [Au25(p-MBA)18]− nanoclusters. The interconversion process between the two isom…

Absorption spectroscopyLigandChemistryGeneral Chemical EngineeringBiochemistry (medical)Intermolecular forceCationic polymerizationGeneral ChemistryPhotochemistryBiochemistryNanoclustersMetalMolecular dynamicsCrystallographyAdsorptionvisual_artMaterials Chemistryvisual_art.visual_art_mediumEnvironmental ChemistryMoleculeDensity functional theoryIsomerizationChem
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Some aspects of the solid state physics of yellow arsenic

1996

Absorption spectroscopychemistryPolymerizationSolid-state physicsChemical engineeringAnnealing (metallurgy)Yellow arsenicchemistry.chemical_elementCondensed Matter PhysicsArsenicElectronic Optical and Magnetic Materialsphysica status solidi (b)
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Effect of short-chain alcohols on surfactant-mediated reversed-phase liquid chromatographic systems.

2010

The behaviour of β-blockers in a reversed-phase liquid chromatographic (RPLC) column with mobile phases containing a short-chain alcohol (methanol, ethanol or 1-propanol), with and without the surfactant sodium dodecyl sulphate (SDS), was explored. Two surfactant-mediated RPLC modes were studied, where the mobile phases contained either micelles or only surfactant monomers at high concentration. Acetonitrile was also considered for comparison purposes. A correlation was found between the effects of the organic solvent on micelle formation (monitored by the drop weight procedure) and on the nature of the chromatographic system (as revealed by the retention, elution strength and peak shape of…

AcetonitrilesAdrenergic beta-Antagonists1-PropanolBiochemistryMicelleAnalytical ChemistryHydrophobic effectchemistry.chemical_compoundSurface-Active AgentsPulmonary surfactantPhase (matter)AcetonitrileMicellesChromatography Reverse-PhaseChromatographyEthanolElutionChemistryMethanolOrganic ChemistryCationic polymerizationSodium Dodecyl SulfateGeneral MedicineReversed-phase chromatographyAlcoholsData Interpretation StatisticalJournal of chromatography. A
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Submicellar and micellar reversed-phase liquid chromatographic modes applied to the separation of beta-blockers.

2009

The behaviour of a reversed-phase liquid chromatographic (RPLC) system (i.e. elution order, resolution and analysis time), used in the analysis of β-blockers with acetonitrile-water mobile phases, changes drastically upon addition of an anionic surfactant (sodium dodecyl sulphate, SDS). Surfactant monomers cover the alkyl-bonded phase in different extent depending on the concentration of both modifiers, in the ranges 1 × 10-3-0.15 M SDS and 5-50% acetonitrile. Meanwhile, the surfactant is dissolved in the mobile phase as free monomers, associated in small clusters or forming micelles. Four characteristic RPLC modes are yielded, with transition regions between them: hydro-organic, micellar, …

AcetonitrilesAdrenergic beta-AntagonistsAnalytical chemistryBiochemistryMicelleSensitivity and SpecificityAnalytical Chemistrychemistry.chemical_compoundPulmonary surfactantSurfactant-mediated chromatographic systemsPhase (matter)Sodium dodecyl sulphateSelectivityAcetonitrileAcetonitrileMicellesChromatographyElutionChemistryOrganic ChemistryCationic polymerizationAnalysis timeSodium Dodecyl SulfateGeneral MedicineReversed-phase chromatographyDirect transfer mechanismModels ChemicalCritical micelle concentrationSolventsβ-BlockersAlgorithmsChromatography LiquidJournal of chromatography. A
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Performance of different C18 columns in reversed-phase liquid chromatography with hydro-organic and micellar-organic mobile phases

2014

Column selection in reversed-phase liquid chromatography (RPLC) can become a challenge if the target compounds interact with the silica-based packing. One of such interactions is the attraction of cationic solutes to the free silanols in silica-based columns, which is a slow sorption-desorption interaction process that gives rise to tailed and broad peaks. The effect of silanols is minimised by the addition of a competing agent in the mobile phase, such as the anionic surfactant sodium dodecyl sulphate (SDS). In micellar-organic RPLC, the adsorption of an approximately fixed amount of SDS monomers gives rise to a stable modified stationary phase, with properties remarkably different from th…

AcetonitrilesAdrenergic beta-AntagonistsBiochemistryAnalytical ChemistrySurface-Active AgentsAdsorptionPulmonary surfactantPhenolsPhase (matter)Sodium dodecyl sulphateAcetonitrileMicellesChromatography Reverse-PhaseChromatographyElutionChemistryOrganic ChemistryCationic polymerizationC18 columnsSodium Dodecyl SulfateWaterGeneral MedicineReversed-phase chromatographySilanesMicellar liquid chromatographyβ-BlockersAdsorptionSelectivityMicellar liquid chromatography
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Characterization of particle morphology of biochanin A molecularly imprinted polymers and their properties as a potential sorbent for solid-phase ext…

2014

Abstract Molecularly imprinted polymers (MIPs) with biochanin A as a template were obtained using a bulk polymerization with non-covalent imprinting approach. The polymers were prepared in acetonitrile as porogen, using ethylene glycol dimethacrylate (EDMA) as cross-linking agent. The synthesis, with an application of 1′,1′-azobis(cyclohexanecarbonitrile) (ACHN) as an initiator, has been performed thermally. During the synthesis process the effect of different functional monomers such as methacrylic acid (MAA), acrylamide (AA) and 4-vinylpyridine (4-VP) was investigated. The application of nitrogen sorption porosimetry, scanning electron microscopy (SEM), and Fourier transform infrared spec…

AcetonitrilesMaterials scienceNitrogenPolymersPyridinesEthylene glycol dimethacrylateBioengineeringPolymerizationBiochanin ABiomaterialschemistry.chemical_compoundSpectroscopy Fourier Transform Infraredsolid-phase extractionSolid phase extractionFourier transform infrared spectroscopyChromatography High Pressure Liquidchemistry.chemical_classificationphytoestrogensAcrylamideChromatographySolid Phase ExtractionMolecularly imprinted polymerPolymerGenisteinIsoflavonesCross-Linking ReagentschemistryMethacrylic acidMechanics of MaterialsadsorptionMicroscopy Electron ScanningMethacrylatesmolecular imprintingMolecular imprintingNuclear chemistryMaterials Science & Engineering C-Materials for Biological Applications
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Simultaneous production of furfural and levulinic acid from pine sawdust via acid-catalysed mechanical depolymerization and microwave irradiation

2019

In this work pine sawdust was converted into levulinic acid (LA) and furfural. Sawdust was first pre-treated with sulfuric acid-catalysed mechanical depolymerization. The conversion reactions were then performed with microwave heating at 180 °C. To enhance the furfural yield and the efficient separation of furfural and LA, a biphasic water-toluene reaction system was used. The effect of an additional catalyst, AlCl3, on the yield of LA and furfural was also studied. According to the results the pre-treatment method enhanced the yields of LA. In addition, due to the microwave heating the reaction times were short. Additional AlCl3 catalyst enhanced the LA yield, however excellent furfural yi…

Acid catalysismikroaallotMechanical depolymerizationLevulinic acidkemian tekniikkahapotfurfuraalibiomassa (teollisuus)BiomassFurfuralorgaaniset yhdisteetpuu (luonnonmateriaalit)Microwave irradiation
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Double Thermoresponsive Block Copolymers Featuring a Biotin End Group

2010

A poly(oligo(ethylene glycol) monomethyl ether methacrylate)-block-poly(N-isopropyl methacrylamide) (POEGMA-b-PNIPMAM) block copolymer with a biotin end group on the PNIPMAM block as a biotarget was synthesized as a model system for temperature-controlled polymer immobilization. The synthesis was based on RAFT polymerization followed by postpolymerization modification of an activated ester precursor block and an exchange of the dithioester end group within one step. NMR, differential scanning calorimetry (DSC), dynamic light scattering (DLS), and turbidimetry measurements were performed to investigate the stimulus-responsive properties. The double thermoresponsive POEGMA-b-PNIPMAM with biot…

AcrylamidesMagnetic Resonance SpectroscopyCalorimetry Differential ScanningPolymers and PlasticsPolymersRadical polymerizationTemperaturetechnology industry and agricultureBiotinBioengineeringChain transferLower critical solution temperaturePolymerizationBiomaterialschemistry.chemical_compoundEnd-groupchemistryPolymer chemistryMaterials ChemistryCopolymerMethacrylamideReversible addition−fragmentation chain-transfer polymerizationStreptavidinEthylene glycolMicellesBiomacromolecules
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