Search results for "methacrylic acid"

showing 10 items of 71 documents

Blends of polyamide 6 and linear low density polyethylene functionalized with methacrylic acid derivatives

1997

Abstract Morphological, calorimetric, rheological, dielectric and mechanical behaviour of blends made with polyamide 6 (PA6) and linear low density polyethylene (PE) are presented. The PE was functionalized grafting ester and alcohol groups in a Brabender mixer with methacrylic acid derivatives. These groups induce “compatibilization” effects in the blends with respect to blends made with the unfunctionalized polyethylene. The difference effects on the behaviour of the blends of the various functional groups are shown. In particular, the interactions at the interface change depending on the chemical nature of the grafted groups. Ethyl and isobuthyl-methacrylate essentially cause dipolar int…

Materials sciencePolymers and PlasticsHydrogen bondOrganic Chemistrytechnology industry and agricultureGeneral Physics and AstronomyCompatibilizationPolyethyleneCondensation reactionLinear low-density polyethylenechemistry.chemical_compoundchemistryMethacrylic acidPolyamidePolymer chemistryMaterials ChemistryPolymer blendEuropean Polymer Journal
researchProduct

Improvement of the butyl methacrylate-paraffin embedment.

1983

The excellent butyl methacrylate-paraffin method as an embedment for light microscopy has been technically improved. More uniform and reproducible polymerization has been obtained by using a vacuum oven to degas the polymerizing mixture and to replace the air with nitrogen at 650 Torr. The amount of benzoyl peroxide required must be determined for each batch of butyl methacrylate. A teflon lined, reusable metal mold and a method of one-step blocking of tissues in preparation for sectioning are also described.

Materials scienceStaining and LabelingEmbedmentHistological Techniquestechnology industry and agriculturechemistry.chemical_elementBenzoyl peroxideNitrogenButyl methacrylateVacuum furnaceFixativeschemistryChemical engineeringPolymerizationPolymethacrylic AcidsParaffinTorrPolymer chemistryMicroscopymedicineMethacrylatesAnatomymedicine.drugStain technology
researchProduct

Über synthetische Matrizenreaktionen

2007

Molecularly homogeneous, polynuclear phenolic compounds were esterified with acrylic acid and methacrylic acid chlorides. The pcresyl esters of acrylic and methacrylic acid react in high dilution in boiling benzene with a large excess of radicals derived from AIBN in such manner that the growth step of the free-radical polymerization is prevented; this may be denoted a “suppressed” polymerization. The application of these conditions to the previously mentioned poly-nuclear esters results in the formation of molecularly homogeneous cyclooligomers (ladder oligomers). Alkaline hydrolysis of these oligomers permits recovery of the polynuclear phenols and yields molecularly homogeneous oligoacry…

Matrix (chemical analysis)chemistry.chemical_compoundMethacrylic acidchemistryPolymerizationRadicalOrganic chemistryPhenolsAlkaline hydrolysis (body disposal)BenzeneAcrylic acidJournal of Polymer Science Part C: Polymer Symposia
researchProduct

Eine einfache, vollstäundige Veresterung von Oligo[(2-hydroxy-1,3-phenylen)methylen]en mit Methacryloylchlorid

1976

Die Darstellung phenolischer Methacrylsaureester verlauft glatt und mit Reinausbeuten bis zu 95%, wenn die in gekuhltem Benzol (5—10°C) in Gegenwart von Triathylamin gelosten phenolischen Verbindungen mit Methacryloylchlorid umgesetzt werden. So wurden neben drei einfachen Phenylmethacrylaten zehn vollstandig veresterte Oligo[(2-hydroxy-1,3-phenylen)methylen]e erhalten. Phenyl methacrylates can easily be prepared with yields of pure esters up to 95% by reaction of the phenolic compounds with methacryloyl chloride in cooled benzene (5—10°C) in the presence of triethylamine. Three simple phenyl methacrylates and ten oligo[(2-hydroxy-1,3-phenylene)methylene]s completely esterified by methacryl…

Methacryloyl chloridechemistry.chemical_compoundMethacrylic acidChemistryPolymer chemistryMethyleneBenzeneMethacrylateTriethylamineDie Makromolekulare Chemie
researchProduct

Wetting ability of an acetone/based etch rinse adhesive after NaOCl-treatment

2011

Objectives: to evaluate the effect of sodium hypochlorite (NaOCl) treatment on surface dentin roughness (Ra) and contact angle (CA) when using Prime&Bond NT adhesive (PB NT). Study Design: Extracted human third molars were sectioned to expose flat, superficial and deep dentin surfaces. CA and Ra were measured (1) before and (2) after 35% H3PO4 etching, and (3) H3PO4 etching + 5% NaOCl treated for 2 minutes before the application of PB NT. CA was measured by the Axisymmetric Drop Shape Analysis Technique using distilled and deionized water and PB NT. Roughness was evaluated with a profilometer, twelve radial measurements were performed in each treatment surface. Data were analyzed with two-w…

MolarSodium HypochloriteSurface PropertiesDentistryIn Vitro TechniquesAcetoneContact anglechemistry.chemical_compoundPolymethacrylic Acidsstomatognathic systemMaterials TestingBiomaterials and Bioengineering in DentistryDentinmedicineSurface roughnessHumansGeneral DentistryChemistrybusiness.industry:CIENCIAS MÉDICAS [UNESCO]Demineralizationstomatognathic diseasesmedicine.anatomical_structureOtorhinolaryngologySodium hypochloriteDentinUNESCO::CIENCIAS MÉDICASWettabilityMolar ThirdResearch-ArticleSurgeryWettingAdhesivebusinessNuclear chemistry
researchProduct

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
researchProduct

A NANOPARTICULATE DRUG-DELIVERY SYSTEM FOR RIVASTIGMINE: PHYSICO-CHEMICAL AND IN VITRO BIOLOGICAL CHARACTERIZATION

2007

The preparation and characterization of surface-PE Gylated polymeric nanoparticles are described. These systems were obtained by UV irradiation of PHM and PHM-PEG(2000) as an inverse microemulsion, using an aqueous solution of the PHM/PHM-PEG(2000) copolymer mixture as the internal phase and triacetin saturated with water as the external phase, and characterized by dimensional analysis, zeta-potential measurements and XPS. in vitro biological tests demonstrated their cell compatibility and their ability to escape from phagocytosis. Rivastigmine was encapsulated into the nanoparticle structure and drug-release profiles from loaded samples were investigated in PBS at pH = 7.4 and human plasma.

Molecular StructureCell SurvivalUltraviolet RaysPhenylcarbamatesRivastigmineHemolysisPolyethylene GlycolsPOLYMERIC NANOPARTICLES RIVASTIGMINE DRUG DELIVERYDrug Delivery SystemsPolymethacrylic AcidsSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoCell Line TumorDelayed-Action PreparationsHumansNanoparticlesPeptidesTriacetin
researchProduct

Ce:YAG nanoparticles embedded in a PMMA matrix: preparation and characterization

2010

A Ce:YAG-poly(methyl methacrylate) composite was prepared using in situ polymerization by embedding the Ce:YAG nanopowder in a blend of methyl methacrylate (MMA) and 2-methacrylic acid (MAA) monomers and activating the photopolymerization using a radical initiator. The obtained nanocomposite was yellow and transparent. Its characterization was performed using transmission electron microscopy, small angle X-ray scattering, (13)C cross-polarization magic-angle spinning nuclear magnetic resonance, and photoluminescence spectroscopy. Results showed that Ce:YAG nanoparticles are well dispersed in the polymeric matrix whose structure is organized in a lamellar shape. The luminescence properties o…

NanocompositeMaterials scienceNanoparticleSurfaces and InterfacesCe:YAG nanopowders PMMA transparent polymeric composite white LEDs.Condensed Matter Physicschemistry.chemical_compoundPhotopolymerchemistryPolymerizationMethacrylic acidChemical engineeringPolymer chemistryElectrochemistryGeneral Materials ScienceMethyl methacrylateIn situ polymerizationLuminescenceSpectroscopy
researchProduct

Polymeric Selectin Ligands Mimicking Complex Carbohydrates: From Selectin Binders to Modifiers of Macrophage Migration

2016

Novel polymeric cell adhesion inhibitors were developed in which the selectin tetrasaccharide sialyl-LewisX (SLeX ) is multivalently presented on a biocompatible poly(2-hydroxypropyl)methacrylamide (PHPMA) backbone either alone (P1) or in combination with O-sulfated tyramine side chains (P2). For comparison, corresponding polymeric glycomimetics were prepared in which the crucial "single carbohydrate" substructures fucose, galactose, and sialic acid side chains were randomly linked to the PHPMA backbone (P3 or P4 (O-sulfated tyramine)). All polymers have an identical degree of polymerization, as they are derived from the same precursor polymer. Binding assays to selectins, to activated endo…

OligosaccharidesTyramine02 engineering and technologyLigands010402 general chemistry01 natural sciencesCatalysisFucoseInhibitory Concentration 50chemistry.chemical_compoundPolymethacrylic AcidsCell MovementHuman Umbilical Vein Endothelial CellsSide chainHumansTetrasaccharideMethacrylamideSialyl Lewis X AntigenCell adhesionCells CulturedMacrophagesGeneral ChemistrySurface Plasmon ResonanceFlow Cytometry021001 nanoscience & nanotechnologyIn vitro0104 chemical sciencesSialic acidMicroscopy Fluorescence MultiphotonNanomedicinechemistryBiochemistrySelectins0210 nano-technologySelectinAngewandte Chemie International Edition
researchProduct

Mechanical properties of provisional dental materials: A systematic review and meta-analysis

2018

Provisional restorations represent an important phase during the rehabilitation process, knowledge of the mechanical properties of the available materials allows us to predict their clinical performance. At present, there is no systematic review, which supports the clinicians' criteria, in the selection of a specific material over another for a particular clinical situation. The purpose of this systematic review and meta-analysis was to assess and compare the mechanical properties of dimethacrylates and monomethacrylates used in fabricating direct provisional restorations, in terms of flexural strength, fracture toughness and hardness. This review followed the PRISMA guidelines. The searche…

OrthodonticsMultidisciplinaryCochrane collaborationWeb of scienceComputer sciencelcsh:RCorrectionlcsh:Medicine030206 dentistry02 engineering and technology021001 nanoscience & nanotechnologyDental Materials03 medical and health sciences0302 clinical medicineSystematic reviewPolymethacrylic AcidsMeta-analysisMaterials TestingHumanslcsh:QStress Mechanical0210 nano-technologylcsh:SciencePLoS ONE
researchProduct