Search results for "silica"

showing 10 items of 1092 documents

Pumice powder as filler of self-compacting concrete

2015

Abstract An experimental study on the rheological and mechanical properties of self-compacting concrete with pumice powder used as filler additive is presented. Self-compacting concrete (SCC) shows its peculiar characteristics in the fresh state and many researches have been developed with reference to its rheological characteristics paying attention to the techniques of self-compacting properties assessment. One of the most important aspect in concrete mix-design is the type and the amount of fillers with respect to water and cement: this amount has great influence not only on self-compacting properties (fluidity, segregation, etc.), but also on the mechanical properties of the mixture. Vo…

CementMaterials scienceSilica fumeMechanical propertiesBuilding and ConstructionPozzolanSettore ICAR/09 - Tecnica Delle CostruzioniPumiceCompressive strengthRheologyPumiceSelf-compacting concreteUltimate tensile strengthConcrete rheologyGeneral Materials ScienceComposite materialFillerCivil and Structural EngineeringShrinkageConstruction and Building Materials
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Engineering Photocatalytic Cements: Understanding TiO2 Surface Chemistry to Control and Modulate Photocatalytic Performances

2010

The present work addresses the aggregation/dispersion properties of two commercial titanias for application as photocatalysts in concrete technology. A microsized m-TiO2 (average particle size 153.7 ± 48.1 nm) and a nanosized n-TiO2 (average particle size 18.4 ± 5.0 nm) have been tested in different ionic media (Na+, K+, Ca2+, Cl−, SO42−, synthetic cement pore solution) at different pHs and in real cement paste specimens. Results highlighted that ion–ion correlations play a fundamental role in TiO2 particles aggregation in the cement environment. A particle aggregation model derived from TiO2 surface chemistry is proposed here and used to justify such aggregation phenomena in real cement pa…

CementMaterials sciencechemistry.chemical_compoundParticle aggregationAdsorptionchemistryMaterials ChemistryCeramics and CompositesPhotocatalysisParticle sizeCementitiousCalcium silicate hydrateComposite materialDispersion (chemistry)Journal of the American Ceramic Society
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Shear bond strength of debonded ceramic restorations re-cemented by means of a cleaning and retreatment protocol

2019

Background As there is no standard method for re-cementing debonded partial ceramic restorations, the aim of this study was to evaluate the use of a non-invasive thermal protocol for cleaning and retreatment, and to study its influence on shear bond strength. Material and methods Twenty ceramic samples (IPS e.max CAD®) were bonded to composite cement cylinders and underwent a shear bond strength test (G1, n=20). A second group was created (G2, n=20), representing debonded restorations. To simulate debonding, the samples were artificially contaminated with composite cement. After debonding, these underwent a thermal protocol to remove remaining adhesive. After rebonding to the composite ceme…

CementProsthetic DentistryMaterials scienceBond strengthResearchComposite numberSignificant difference:CIENCIAS MÉDICAS [UNESCO]Shear bondvisual_artUNESCO::CIENCIAS MÉDICASLithium disilicatevisual_art.visual_art_mediumAdhesiveCeramicComposite materialGeneral Dentistry
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Intrinsic Acidity of Surface Sites in Calcium Silicate Hydrates and Its Implication to Their Electrokinetic Properties

2014

Calcium Silicate Hydrates (C–S–H) are the major hydration products of portland cement paste. The accurate description of acid–base reactions at the surface of C–S–H particles is essential for both understanding the ion sorption equilibrium in cement and prediction of mechanical properties of the hardened cement paste. Ab initio molecular dynamics simulations at the density functional level of theory were applied to calculate intrinsic acidity constants (pKa’s) of the relevant ≡SiOH and ≡CaOH2 groups on the C–S–H surfaces using a thermodynamic integration technique. Ion sorption equilibrium in C–S–H was modeled applying ab initio calculated pKa’s in titrating Grand Canonical Monte Carlo simu…

CementQuantitative Biology::BiomoleculesChemistryAb initioThermodynamicsThermodynamic integrationSorptionElectrolyteSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionElectrokinetic phenomenachemistry.chemical_compoundPortland cementGeneral EnergylawCalcium silicate550 Earth sciences & geologyPhysical chemistry[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Physical and Theoretical ChemistryPhysics::Chemical PhysicsComputingMilieux_MISCELLANEOUS
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Experimental investigation of calcium silicate hydrate (C-S-H) nucleation

1999

Due to the importance of calcium silicate hydrate (C-S-H) in cement chemistry, its nucleation mode and parameters influencing it were investigated. It has been observed that the C-S-H nucleation follows the general laws governing the nucleation. The degree of supersaturation has been found to be the main parameter controlling homogeneous nucleation rates. The lime concentration in solution, well known to be the most important parameter determining the kinetic, morphological and structural features of C-S-H, also controls the nucleation characteristics of heterogeneous nucleation, i.e. during hydration of cement. The correlation between heterogeneous nucleation of C-S-H and possible final me…

CementSupersaturationInorganic chemistryNucleationThermodynamicsengineering.materialCondensed Matter PhysicsKinetic energyInorganic Chemistrychemistry.chemical_compoundchemistryCalcium silicateMaterials ChemistryengineeringCalcium silicate hydrateHydrateLimeJournal of Crystal Growth
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Hydration of cementitious materials, present and future

2011

This paper is a keynote presentation from the 13th International Congress on the Chemistry of Cement. It discusses the underlying principles of hydration and recent evidence for the mechanisms governing this process in both Portland cements and other cementitious materials. Given the overriding imperative to improve the sustainability of cementitious materials, routes to reducing CO2 emissions are discussed and the impact of supplementary materials on hydration considered. (C) 2011 Elsevier Ltd. All rights reserved.

CementWaste managementChemistry0211 other engineering and technologies02 engineering and technologyBuilding and Construction021001 nanoscience & nanotechnologylaw.inventionchemistry.chemical_compoundPortland cementChemical reaction kinetics13. Climate actionlawInternational congress021105 building & constructionForensic engineeringGeneral Materials ScienceCementitiousCalcium silicate hydrate0210 nano-technologyTricalcium silicateCement and Concrete Research
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SHORT-TERM PROCESSES OF RADIONUCLIDE IMMOBILIZATION IN CEMENT - A CHEMICAL APPROACH

1992

Abstract The ions released in solution by the constituents of cement (principally silicate, aluminate, OH and Ca ions) can combine with the anions and cations from nuclear wastes present in the mixing water to give very insoluble compounds that can fix these ions in the concrete matrix. In order to understand some of the particular physico-chemical processes involved in cement hydration in the presence of analogue elements, tricalcium silicate (C 3 S) was used instead of cement, which is too complex a mixture. It was found that the salt of a chemical analogue, a lanthanide salt, showed some accelerating effects when present in dilute amounts but resulted in large accelerating effects on QS …

Cementchemistry.chemical_classificationAluminateInorganic chemistry0211 other engineering and technologiesSalt (chemistry)02 engineering and technology021001 nanoscience & nanotechnologyAlkali metalPollution6. Clean waterSilicatelaw.inventionchemistry.chemical_compoundPortland cement[SPI.GCIV]Engineering Sciences [physics]/Civil EngineeringchemistryGeochemistry and Petrologylaw021105 building & constructionEnvironmental ChemistryHydroxide0210 nano-technologyHydrateNuclear chemistry
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Retention of alkali ions by hydrated low-pH cements: Mechanism and Na+/K+ selectivity

2013

Low-pH cements, also referred to as low-alkalinity cements, can be designed by replacing significant amounts of Portland cement by pozzolanic materials. Their pore solution is characterized by a pH near 11, and an alkali concentration much lower than that of Portland cement. This work investigates the retention of sodium and potassium by a hydrated low-pH cement comprising 60% Portland cement and 40% silica fume. It is shown that sorption of potassium is higher than that of sodium and mainly results from counterion charge balancing of the C-S-H negative surface charge. To explain the greater retention of potassium compared to sodium, it is postulated that potassium, unlike sodium, may enter…

Cementchemistry.chemical_classificationMaterials scienceSilica fumeSodiumPotassiumInorganic chemistrytechnology industry and agriculturechemistry.chemical_elementBuilding and ConstructionPozzolanAlkali metallaw.inventionPortland cementchemistrylawGeneral Materials ScienceCounterionCement and Concrete Research
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Investigations on The Micro-Structure of Hardened Cement Pastes

1988

Abstract Creep is a mechanical property, that has to be taken into account in the design of concrete constructions. Earlier studies showed that creep of concrete, among other things, depends on the relative humidity of the environment and on the type of cement used. The origin of creep lies in the hydrated cement paste, which is present between the aggregates. This paper, based on a thesis of H.H. Willems (ref. 1) deals with the relation between the creep behaviour and the microstructure of hardened Portland (PC) and Portland-blastfurnace cement (PBC) pastes. At several relative humidities shrinkage and creep experiments have been performed with thin-walled hollow cylindrical specimens. Nex…

Cementchemistry.chemical_compoundMaterials sciencechemistryCreepRelative humiditySorptionComposite materialMicrostructureMicro structureSilicateShrinkage
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Bond strength of selected composite resin-cements to zirconium-oxide ceramic

2012

Objectives: The aim of this study was to evaluate bond strengths of zirconium-oxide (zirconia) ceramic and a selection of different composite resin cements. Study Design: 130 Lava TM cylinders were fabricated. The cylinders were sandblasted with 80 μm aluminium oxide or silica coated with CoJet Sand. Silane, and bonding agent and/or Clearfil Ceramic Primer were applied. One hundred thirty composite cement cylinders, comprising two dual-polymerizing (Variolink II and Panavia F) and two autopolymerizing (Rely X and Multilink) resins were bonded to the ceramic samples. A shear test was conducted, followed by an optical microscopy study to identify the location and type of failure, an elec…

CeramicsMaterials scienceComposite numberSurface treatmentOdontologíaDental bondingComposite ResinsDental Materialschemistry.chemical_compoundCIENCIA DE LOS MATERIALES E INGENIERIA METALURGICABiomaterials and Bioengineering in DentistryMaterials TestingCubic zirconiaCeramicComposite materialGeneral DentistryCementBond strengthShear bond strengthDental BondingSilica coating:CIENCIAS MÉDICAS [UNESCO]SilaneCiencias de la saludResin CementsOtorhinolaryngologychemistryvisual_artUNESCO::CIENCIAS MÉDICASvisual_art.visual_art_mediumZirconia ceramicsResearch-ArticleSurgeryZirconiumAdhesivePhosphate monomer
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