Search results for "polymerization"

showing 10 items of 1689 documents

Reduction of Polymerization Shrinkage Stress and Marginal Microleakage Using Soft-Start Polymerization

2003

Purpose: This study evaluated the influence of a soft-start light-curing exposure on polymerization shrinkage stress and marginal integrity of adhesive restorations. Materials and Methods: Six resin-based composites (Pertac II, Tetric Ceram, Definite, Surefil, Solitaire, and Visio-Molar) were adhesively bonded to a cylindrical cavity (n = 9 per material/light) in a photoelastic material. Visible light-curing was applied using either the standard polymerization mode (800 mW/cm2 exposure duration 40 s) of the curing light (Elipar TriLight, 3M ESPE) or the exponential mode from the same device (ramp-curing: 150 mW/cm2 to 800 mW/cm2 within the first 15 s of a total curing time of 40 s). Polymer…

MolarTime FactorsMaterials scienceSiloxanesPolymersSurface PropertiesComposite ResinsPhosphatesAcetonePolymethacrylic AcidsHardnessMaterials TestingHumansBisphenol A-Glycidyl MethacrylatePhosphoric AcidsComposite materialDental EnamelGeneral DentistryLightingCuring (chemistry)ShrinkageDental CementumDental LeakageEthanolEnamel paintTerpenesQuartzDental Marginal AdaptationHardnessDental Marginal AdaptationResin CementsPolymerizationDentin-Bonding Agentsvisual_artvisual_art.visual_art_mediumMethacrylatesAdhesiveJournal of Esthetic and Restorative Dentistry
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Nebenreaktionen der radikalisch ausgelösten Cyclisierung von 2,2′-Methylen-bis(4-methyl-1,2-phenylen)-dimethacrylat

1979

2,2′-Methylene-bis(4-methyl-1,2-phenylene) dimethacrylate (1) was reacted with an excess of 2,2′-azoiso-butyronitrile (mole ratio 1:15) highly diluted in boiling benzene. The reaction products were separated by column chromatography. It was found that the 1-cyano-1-methylethyl radical induced the cyclization of 1 to yield the product of a head to tail addition (2) in 55% yield. In addition, the product of a head to head addition (3) was isolated in 4% yield. 35% of 1 reacted in the same way as it has already been observed as suppression of polymerization in the case of p-tolyl methacrylate to give the products 4 and 5. The structures of the products were confirmed by elemental analyses, by …

Mole ratioPolymers and PlasticsChemistryHead to headMethacrylateMedicinal chemistrychemistry.chemical_compoundColloid and Surface ChemistryColumn chromatographyPolymerizationYield (chemistry)Polymer chemistryMaterials ChemistryProton NMRPhysical and Theoretical ChemistryBenzeneColloid and Polymer Science
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Influence of chain length on the molecular dynamics of an aliphatic ionene

1998

An aliphatic random copolymer ionene (a cationic polyelectrolyte with N + in the repeat unit), was fractionated with the continuous polymer fractionation and investigated for its molecular weight dependent properties. The fractions were analyzed with GPC and capillary viscometry for their molecular weight. Glass transition temperatures were determined with DSC and a strong molecular weight dependence was observed, but no influence in the ionic conductivity was observed. The temperature dependency of ionic conductivity in ionenes is described.

Molecular dynamicsPolymers and PlasticsChemistryGeneral Chemical EngineeringPolymer chemistryCationic polymerizationCopolymerPhysical chemistryViscometerIonic conductivityPolymer fractionationGlass transitionPolyelectrolyteActa Polymerica
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Diene-Containing Half-Sandwich MoIII Complexes as Ethylene Polymerization Catalysts: Experimental and Theoretical Studies

2001

International audience; Seventeen-electron compounds of Mo III having the general formula [(h 5-C 5 R 5)Mo(h 4-diene)X 2 ] (R H, Me; diene butadiene, iso-prene, or 2,3-dimethylbutadiene; X Cl, CH 3) are a new class of ethylene polymerization catalysts. The polyethy-lene obtained shows a bimodal distribution , the major weight fraction being characterized by very long (M around 10 6) and highly linear polymer chains. The newly prepared pentamethylcyclo-pentadienyl (Cp*) derivatives are more active than the cyclopentadienyl (Cp) derivatives, but much less active than previously investigated niobium III compounds having the same stoichiometry. On the other hand, the turnover frequency of the a…

MolybdenumAgostic interactionEthylene polymerizationChain propagationbiologyChemistryNiobiumOrganic ChemistryActive site[CHIM.CATA]Chemical Sciences/CatalysisGeneral ChemistryPhotochemistryHeterolysisCatalysisDensity functional calculationsCrystallography[CHIM.POLY]Chemical Sciences/PolymersCyclopentadienyl complexPolymerizationbiology.protein[CHIM.COOR]Chemical Sciences/Coordination chemistryDensity functional theoryMulliken population analysisCyclopentadienyl ligandsChemistry - A European Journal
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Preparation of organic monolithic columns in polytetrafluoroethylene tubes for reversed-phase liquid chromatography

2017

[EN] In this work, a method for the preparation and anchoring of polymeric monoliths in a polytetrafluoroethylene (PTFE) tubing as a column housing for microbore HPLC is described. In order to assure a covalent attachment of the monolith to the inner wall of the PTFE tube, a two-step procedure was developed. Two surface etching reagents, a commercial sodium naphthalene solution (Fluoroetch®), or mixtures of H2O2 and H2SO4, were tried and compared. Then, the obtained hydroxyl groups on the PTFE surface were modified by methacryloylation. Attenuated total reflectance Fourier-transform infrared (ATR-FTIR) spectroscopy and scanning electron microscopy (SEM) confirmed the successful modification…

Monolithic HPLC columnMicrobore column02 engineering and technology01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compoundSurface modificationQUIMICA ANALITICAEnvironmental ChemistryMonolith attachmentMonolithReversed-phase liquid chromatographyPolytetrafluoroethyleneSpectroscopychemistry.chemical_classificationChromatography Reverse-PhasegeographyChromatographygeography.geographical_feature_categoryPolytetrafluoroethyleneChemistry010401 analytical chemistryPolymer monolithEquipment DesignPolymer021001 nanoscience & nanotechnology0104 chemical sciencesChemical engineeringPolymerizationAttenuated total reflectionSurface modificationAlkylbenzenes0210 nano-technologyAnalytica Chimica Acta
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Photografted fluoropolymers as novel chromatographic supports for polymeric monolithic stationary phases

2018

[EN] In this study, porous polymer monoliths were in situ synthesized in fluoropolymers tubing to prepare microbore HPLC columns. To ensure the formation of robust homogeneous polymer monoliths in these housing supports, the inner surface of fluoropolymer tubing was modified in a two-step photografting process. Raman spectroscopy and scanning electron microscopy (SEM) confirmed the successful modification of the inner poly(ethylene-co-tetrafluoroethylene) (ETFE) wall and the subsequent attachment of a monolith onto the wall. Poly(glycidyl methacrylate-co-divinylbenzene), poly(butyl methacrylate-co-ethyleneglycol dimethacrylate) and poly(styrene-co-divinylbenzene) monoliths were in situ synt…

Monolithic columnMonolithic HPLC columnFluoropolymer02 engineering and technology01 natural sciencesAnalytical Chemistrychemistry.chemical_compoundETFEPhotograftingQUIMICA ANALITICAMonolithReversed-phase liquid chromatographyAlkylchemistry.chemical_classificationgeographyEthylene-tetrafluoroethylenegeography.geographical_feature_categoryChromatography010401 analytical chemistryPolymer021001 nanoscience & nanotechnology0104 chemical scienceschemistryPolymerizationPhotograftingFluoropolymer0210 nano-technology
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A new route for the preparation of flexible skin–core poly(ethylene-co-acrylic acid)/polyaniline functional hybrids

2011

Abstract Surface modification of polymeric films is a way to obtain final products with high performance for many specific and ad hoc tailored applications, e.g. in functional packaging, tissue engineering or (bio)sensing. The present work reports, for the first time, on the design and development of surface modified ethylene–acrylic acid copolymer (EAA) films with polyaniline (PANI), with the aim of inducing electrical conductivity and potentially enable the electronic control of a range of physical and chemical properties of the film surface, via a new “grafting from” approach. In particular, we demonstrate that PANI was successfully polymerized and covalently grafted onto flexible EAA su…

MorphologyMaterials Chemistry2506 Metals and AlloysMaterials sciencePolymers and PlasticsPolyanilineGeneral Chemical EngineeringHybrid polymersBiochemistrychemistry.chemical_compoundX-ray photoelectron spectroscopyPolyanilinePolymer chemistryChemical surface modificationElectrical conductivityPolyaniline Chemical surface modification Hybrid polymers Morphology Electrical conductivityMaterials ChemistryCopolymerEnvironmental ChemistryChemical Engineering (all)Fourier transform infrared spectroscopyAcrylic acidChemistry (all)General ChemistryChemical engineeringchemistryPolymerizationSurface modificationSettore CHIM/07 - Fondamenti Chimici Delle TecnologieChemical surface modification; Electrical conductivity; Hybrid polymers; Morphology; Polyaniline; Materials Chemistry2506 Metals and Alloys; Polymers and Plastics; Chemistry (all); Chemical Engineering (all); Environmental Chemistry; BiochemistryHybrid materialReactive and Functional Polymers
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2015

AbstractThe synthesis, characterization and evaluation in solid-state devices of a series of 8 cationic iridium complexes bearing different numbers of methoxy groups on the cyclometallating ligands are reported. The optoelectronic characterization showed a dramatic red shift in the absorption and the emission and a reduction of the electrochemical gap of the complexes when a methoxy group was introduced para to the Ir-C bond. The addition of a second or third methoxy group did not lead to a significant further red shift in these spectra. Emission maxima over the series ranged from 595 to 730 nm. All complexes possessing a motif with a methoxy group at the 3-position of the cyclometalating l…

MultidisciplinaryPhotoluminescenceChemistryLigandCationic polymerizationchemistry.chemical_element02 engineering and technologyElectroluminescence010402 general chemistry021001 nanoscience & nanotechnologyElectrochemistryPhotochemistry01 natural sciencesSpectral line0104 chemical sciencesPolar effectIridium0210 nano-technologyScientific Reports
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Kinetics of the Biosynthesis of Cellulose in Cotton Bolls by Different Light Intensities

1966

PREVIOUS kinetic investigations of the biosynthesis of cellulose in higher plants suggested that the secondary wall cellulose is synthesized by a structure-controlled mechanism (template mechanism)1–5. In order to confirm my assumption I changed the reaction rate by varying the intensity of illumination of the cotton plants. Cotton plants (Gossypium herbaceum) were grown in a glass-house at a mean temperature of 25° C (the night temperatures never were less than 18° C). The intensity of illumination amounted to 4,000, 15,000 and 60,000 lux respectively (mean values). The time of maturity was calculated from the time the flowers were fertilized. Bolls of different maturities were picked, imm…

MultidisciplinarybiologyKineticsfood and beveragesDegree of polymerizationPhotochemistrybiology.organism_classificationGossypium herbaceumReaction ratechemistry.chemical_compoundHorticulturechemistryBiosynthesisCelluloseNature
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1-n-Butyl-3-methylimidazolium-2-carboxylate: a versatile precatalyst for the ring-opening polymerization of ε-caprolactone and rac-lactide under solv…

2013

The ring-opening polymerization of ε-caprolactone (ε-CL) and rac-lactide (rac-LA) under solvent-free conditions and using 1-n-butyl-3-methylimidazolium-2-carboxylate (BMIM-2-CO2) as precatalyst is described. Linear and star-branched polyesters were synthesized by successive use of benzyl alcohol, ethylene glycol, glycerol and pentaerythritol as initiator alcohols, and the products were fully characterized by 1H and 13C{1H} NMR spectroscopy, gel permeation chromatography (GPC), and differential scanning calorimetry (DSC). BMIM-2-CO2 acts as an N-heterocyclic carbene precursor, resulting from in situ decarboxylation, either by heating under vacuo (method A) or by addition of NaBPh4 (method B)…

N-heterocarbene precursorLactideLetterOrganic ChemistryRing-opening polymerizationPentaerythritollcsh:QD241-441chemistry.chemical_compoundChemistryimidazolium-2-carboxylateschemistryPolymerizationlcsh:Organic chemistryBenzyl alcoholgreen polymerization reactionPolymer chemistryaliphatic polyestersOrganic chemistrylcsh:QorganocatalysisCarboxylatelcsh:ScienceCaprolactoneEthylene glycolBeilstein Journal of Organic Chemistry
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