Search results for "Bonding"

showing 10 items of 996 documents

Current dental adhesives systems. A narrative review.

2012

Adhesive dentistry is based on the development of materials which establish an effective bond with the tooth tissues. In this context, adhesive systems have attracted considerable research interest in recent years. Successful adhesive bonding depends on the chemistry of the adhesive, on appropriate clinical handling of the material as well as on the knowledge of the morphological changes caused on dental tissue by different bonding procedures. This paper outlines the status of contemporary adhesive systems, with particular emphasis on chemical characteristics and mode of interaction of the adhesives with enamel and dentinal tissues. Dental adhesives are used for several clinical application…

Adhesive bondingPolyurethanesAcrylic ResinsDentistryDental CementsComposite ResinsComposite resinstomatognathic systemSettore MED/28 - Malattie OdontostomatologicheDrug DiscoveryAdhesive systemHumansDental EtchingDental EnamelPharmacologyOrthodonticsEnamel paintbusiness.industryDentineDental BondingDental Adhesivesstomatognathic diseasesEnamelvisual_artDentin-Bonding AgentsDental EtchingDentinvisual_art.visual_art_mediumNarrative reviewAdhesivebusinessDental adhesivePhosphoric acidCurrent pharmaceutical design
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Buildup of Ultrathin Multilayer Films by a Self-Assembly Process: II. Consecutive Adsorption of Anionic and Cationic Bipolar Amphiphiles and Polyelec…

1991

We have recently reported on the consecutive physisorption of anionic and cationic bipolar amphiphiles onto charged surfaces, adsorbed out of aqueous solutions [1]. Here, we extend our previous concept to multipolar compounds such as polyelectrolytes. In contrast to the bipolar amphiphile system, it is not necessary to separate single charges by a rigid unit, when the polyelectrolyte is adsorbed from sufficiently concentrated solutions. In this case the physisorbed layer does not bind with all ionic groups to the surface and exposes free ionic groups at the new film/solution interface. Therefore a polyelectrolyte layer can replace a layer of bipolar amphiphiles in the consecutive buildup of…

AdsorptionAqueous solutionMaterials scienceChemical engineeringGeneral Chemical EngineeringMonolayerAmphiphileIonic bondingNanotechnologySurface chargeSelf-assemblyPolyelectrolyteBerichte der Bunsengesellschaft für physikalische Chemie
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Retention of Vanadium(V), Molybdenum(VI) and Tungsten(VI) by Kaolin

1993

Abstract The ability of kaolin (approximately H2Al2Si2O8 · H2O), a well known clay mineral constituent, to retain V(V) andMo(VI) species from 10−5 and 10−4 M solutions, and W(VI) species from 10−4 M solutions was investigated in the pH range 2–7.5 using a solid/liquid ratio 1:100 (w:v). The equilibration time in the adsorption studies was 72 h, and the shaking time in the desorption studies was 17 h. 0.02 M KCl was used as ionic medium and desorbing liquid. V(V), Mo(VI) and W(VI) were all retained by kaolin to some extent, and the amounts of the elements which could be washed away from kaolin with 0.02 M KCl were very small. The pH dependence of the adsorption was considerable: when added a…

AdsorptionChemistryMolybdenumDesorptionInorganic chemistrySoil Sciencechemistry.chemical_elementKaoliniteIonic bondingVanadiumTungstenClay mineralsAgronomy and Crop ScienceActa Agriculturae Scandinavica, Section B - Soil & Plant Science
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<title>Large-scale computer simulations of metal/oxide interfaces with defects</title>

2003

Ab initio slab simulations have been performed for silver adhesion to the perfect and defective MgO(001) surfaces. For 1/4 Ag monolayer (ML) coverage of perfect substrate, we observe small silver adhesion energies over both O2- and Mg2+ ions on a regular MgO(001) substrate (0.23 and 0.22 eV per Ag atom, respectively), with negligible interfacial charge transfer towards metal atoms. For larger Ag coverages (beginning with 1/2 ML), silver adsorption over regular O2- ions is much more favorable. We demonstrate that point surface defects on a magnesia surface increase markedly the metal adhesion energy and cause a redistribution of the electron density across the interface. The results for elec…

AdsorptionMaterials sciencePhysisorptionVacancy defectAtomMonolayerBinding energyAnalytical chemistryIonic bondingAtomic physicsIonSPIE Proceedings
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Effect of self-etching primer/adhesive and conventional bonding on the shear bond strength in metallic and ceramic brackets

2011

Introduction: Bracket debonding from the tooth surface is a common problem in fixed orthodontics. The aims of the present study were to assess the bond strength and failure sites in two ways of bonding technique, with metallic and ceramic brackets. Material and Methods: One hundred premolars were assigned to 4 groups of 25 each: Group A, metallic brackets/ conventional procedure; Group B, metallic brackets/Transbond XT; Group C, ceramic brackets/conventional procedure; and Group D, ceramic brackets/Transbond XT. Transbond XT composite paste was used for bracket bonding and cured by conventional light-cure device. Specimens were subjected to thermocycling. One week after bonding shearing for…

AdultMaterials scienceAdolescentOrthodontic BracketsDentistryDental bondingIn Vitro TechniquesYoung AdultClinical and Experimental DentistryAdhesivesMaterials TestingShear strengthHumansCeramicComposite materialGeneral DentistryShearing (physics)business.industryBond strengthBracketDental BondingTooth surfaceStainless Steel:CIENCIAS MÉDICAS [UNESCO]Resin CementsOtorhinolaryngologyvisual_artUNESCO::CIENCIAS MÉDICASDental Etchingvisual_art.visual_art_mediumSurgeryResearch-ArticleAdhesivebusinessShear Strength
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How can droplet formation occur in endodontically treated teeth during bonding procedures?

2008

PURPOSE: The aim of this in vivo study was to clarify how blistering formation occurs along intraradicular dentin bonded interfaces. MATERIALS AND METHODS: Patients were selected and post space was prepared in vivo in endodontically treated teeth. Post space was etched, dried with ethanol, and bonded with one of the following adhesive systems: All Bond 2, XP-Bond, Clearfil SE Bond, Xeno III. The four adhesives were considered as representative of each bonding system class. An additional group was prepared with phosphoric acid treatment + application of Pre-Bond unfilled resin of All Bond 2, without the use of the primer agent. Etching was avoided for self-etching materials. Replicas of the …

AdultTooth NonvitalEthanolSurface PropertiesDental BondingMiddle Agedadhesive permeability simplified adhesive root canal droplet formationResin CementsAcid Etching DentalSettore MED/28 - Malattie OdontostomatologicheDentin-Bonding AgentsDentinMicroscopy Electron ScanningSolventsHumansMethacrylatesReplica TechniquesPhosphoric AcidsDental Pulp CavityAgedPost and Core Technique
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Modelling of proton and metal exchange in the alginate biopolymer.

2005

Acid-base behaviour of a commercial sodium alginate extracted from brown seaweed (Macrocystis pyrifera) has been investigated at different ionic strengths (0.1or=I/mol l(-1)or=1.0) and in different supporting electrolytes (Et4NI, NaCl, KCl, LiCl, NaCl+MgCl2), with the aim of examining the influence of ionic medium on the proton-binding capacity and of quantifying the strength of interaction with light metal ions in the perspective of speciation studies in natural aqueous systems. Potentiometric ([H+]-glass electrode) and titration calorimetric data were expressed as a function of the dissociation degree (alpha) using different models (Henderson-Hasselbalch modified, Högfeldt three parameter…

Alginic acid; Proton- and metal-binding capacity; Thermodynamic parameters; Ionic strength dependence; Models for medium dependence and ion associationProton bindingAlginatesIonic strength dependenceInorganic chemistryPotentiometric titrationIonic bondingProtonationElectrolytePhaeophytaBiochemistryAnalytical ChemistryBiopolymersGlucuronic Acidalginic acid proton and metal-binding capacity Thermodynamics parameters Ionic strength dependence models for medium dependence and ion associationAlginic acidMagnesium ionAqueous solutionMolecular StructureChemistryHexuronic AcidsProton- and metal-binding capacityThermodynamic parametersIonic strengthMetalsProtonsModels for medium dependence and ion associationAnalytical and bioanalytical chemistry
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The transport of ions across monoolein bilayers mediated by synthetic macrocyclic carriers

1989

The efficiency as carriers for the alkali and the alkaline earth ions across monoolein bilayers of three macrocyclic compounds has been investigated by conductometric measurements. The results show that although the three compounds have the optimum cavity size for fitting potassium and barium cations, their efficiency in ionic transport is quite different. These discrepancies are rationalized on the basis of the overlap of the water-diazacrown and cation-ligand interactions on the carrier mechanism.

Alkaline earth metalChemistryBilayerInorganic chemistryBiophysicsIonophoreIonic bondingchemistry.chemical_elementBariumAlkali metalBiochemistryIonMembranePhysical and Theoretical ChemistryMolecular BiologyJournal of Solution Chemistry
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Nonporous Organic Solids Capable of Dynamically Resolving Mixtures of Diiodoperfluoroalkanes

2009

Halogen bonding has increasingly facilitated the assembly of diverse host-guest solids. Here, we show that a well-known class of organic salts, bis(trimethylammonium) alkane diiodides, can reversibly encapsulate α,ω-diiodoperfluoroalkanes (DIPFAs) through intermolecular interactions between the host's I – anions and the guest's terminal iodine substituents. The process is highly selective for the fluorocarbon that forms an I – ···I(CF 2 ) m I···I – superanion that is matched in length to the chosen dication. DIPFAs that are 2 to 12 carbons in length (common industrial intermediates) can thereby be isolated from mixtures by means of crystallization from solution upon addition of the dissolv…

Alkanechemistry.chemical_classificationMultidisciplinaryHalogen bondChemistryInorganic chemistryIonic bondingCrystal structurelaw.inventionInclusion compoundDicationchemistry.chemical_compoundlawMoleculeCrystallizationScience
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Thermodynamic Study of Small Hydrophobic Ions at the Water–Lipid Interface

2001

Abstract The thermodynamics of binding of two small hydrophobic ions such as norharman and tryptophan to neutral and negatively charged small unilamellar vesicles was investigated at pH 7.4 using fluorescence spectroscopy. Vesicles were formed at room temperature from dimyristoyl phosphatidylcholine (DMPC) or DMPC/dimyristoylphosphatidic acid and DMPC/dimyristoylphosphatidylglycerol. The changes in fluorescence properties were used to obtain association isotherms at variable membrane surface negative charge and at different ionic strengths. The binding of both ions was found to be quantitatively enhanced as the percentage of negative phospholipid increases in the membrane. Also, a decrease …

Analytical chemistryPhospholipidPhosphatidic AcidsIonic bondingBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryIon bindingElectrochemistryLipid bilayerUnilamellar LiposomesIonsChromatographyVesicleTryptophanBinding constantSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsPartition coefficientHarminechemistryPartition equilibriumThermodynamicslipids (amino acids peptides and proteins)DimyristoylphosphatidylcholineHydrophobic and Hydrophilic InteractionsCarbolinesJournal of Colloid and Interface Science
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