Search results for "Chemical engineering"

showing 10 items of 5892 documents

On the physico-chemical evolution of low-pH and CEM I cement pastes interacting with Callovo-Oxfordian pore water under its in situ CO2 partial press…

2014

International audience; Abstract Within the framework of geological repositories for radioactive waste, structural concretes must be adapted to the underground chemical conditions. CEM I cement-based materials are characterised by high pH that may produce an alkaline plume in the near-field of the repository. In order to avoid this problem, low-pH cements have been designed. This study compares the physico-chemical behaviour of a low-pH material with a CEM I cement paste, both being subjected to leaching by an aqueous solution. An original experimental setup was designed to reproduce the underground conditions using a specific CO2 regulation device. Under these conditions, the low-pH materi…

CementMaterials scienceAqueous solutionta114Precipitation (chemistry)Microstructure (B) Carbonation (C) Cement paste (D) Durability (C) Degradation (C)MineralogyRadioactive wasteBuilding and Construction010501 environmental sciences010502 geochemistry & geophysicsMicrostructure01 natural sciencesPore water pressureChemical engineeringGeneral Materials Science[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Leaching (metallurgy)Porosity0105 earth and related environmental sciencesCement and Concrete Research
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Two-Step Nucleation Process of Calcium Silicate Hydrate, the Nanobrick of Cement

2018

Despite a millennial history and the ubiquitous presence of cement in everyday life, the molecular processes underlying its hydration behavior, like the formation of calcium–silicate–hydrate (C–S–H), the binding phase of concrete, are mostly unexplored. Using time-resolved potentiometry and turbidimetry combined with dynamic light scattering, small-angle X-ray scattering, and cryo-TEM, we demonstrate C–S–H formation to proceed via a complex two-step pathway. In the first step, amorphous and dispersed spheroids are formed, whose composition is depleted in calcium compared to C–S–H and charge compensated with sodium. In the second step, these amorphous spheroids crystallize to tobermorite-typ…

CementMaterials scienceGeneral Chemical EngineeringNucleation02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAmorphous solidlaw.inventionchemistry.chemical_compoundchemistryDynamic light scatteringChemical engineeringlawPhase (matter)PercolationMaterials Chemistry[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Calcium silicate hydrateCrystallization0210 nano-technologyComputingMilieux_MISCELLANEOUS
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Studies on mechanism and physico-chemical parameters at the origin of the cement setting II. Physico-chemical parameters determining the coagulation …

1996

The physico-chemical parameters determining the coagulation of cements grains previously identified as the first fundamental process of cement setting have been investigated in diluted suspensions using an adapted granulometric method. The analysis of the influence of the ionic concentration in solution on the coagulation reveals that calcium concentration is the parameter which determines the particle interactions. There exists a minimum critical concentration of calcium ions in solution which is required to occur the coagulation of cement particles and a dispersive effect appears for very high concentrations. The results are discussed in relation with DLVO theory and specific interactions.

CementMaterials scienceMetal ions in aqueous solutionIonic bondingMineralogychemistry.chemical_elementBuilding and ConstructionCalciumChemical engineeringchemistryParticle-size distributionParticleCoagulation (water treatment)DLVO theoryGeneral Materials ScienceCement and Concrete Research
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Physico-chemical parameters determining hydration and particle interactions during the setting of silicate cements

1997

Abstract Hydration of tricalcium silicate (Ca 3 SiO 5 ), the pure phase used as a model of the portland cements, is the chemical process leading to the formation of hydrates, while setting is a definite time event corresponding to the change of the paste from the soft to the hard state. Setting results from interactions between anhydrous or very partially hydrated particles. The analysis of these interactions leads to the identification of two fundamental steps: the coagulation of cement grains during the first minutes following the mixing and the rigidification of the coagulated structure which arises simultaneously with the acceleration of the calcium silicate hydrates (CSH) formation. …

CementMaterials scienceMineralogyGeneral Chemistryengineering.materialCondensed Matter PhysicsSilicatechemistry.chemical_compoundchemistryChemical engineeringCalcium silicateengineeringCoagulation (water treatment)ParticleGeneral Materials ScienceCalcium silicate hydrateSolubilityLimeSolid State Ionics
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Formation of the C−S−H Layer during Early Hydration of Tricalcium Silicate Grains with Different Sizes

2005

Portland cement is a mixture of solid phases which all react with water. Tricalcium silicate (Ca3SiO5) is its main component and is often used in model systems to study cement hydration. It is generally recognized that setting and hardening of cement are due to the formation, by a dissolution-precipitation process, of a calcium silicate hydrate (C-S-H) on anhydrous grains during Ca3SiO5 hydration. The purpose of this paper is to study the effect of Ca3SiO5 particle size on the nucleation-growth process of C-S-H. An experimental study of the rate of hydration by using different grain sizes under controlled conditions has been performed. The experimental data have been compared with results o…

CementMaterials scienceMineralogySurfaces Coatings and Filmslaw.inventionchemistry.chemical_compoundPortland cementchemistryChemical engineeringlawMaterials ChemistryHardening (metallurgy)AnhydrousSolid phasesParticle sizePhysical and Theoretical ChemistryCalcium silicate hydrateTricalcium silicateThe Journal of Physical Chemistry B
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Physicochemical parameters - hydration performance relationship of the new endodontic cement MTA Repair HP

2019

Background To characterize the chemical composition and textural parameters of the MTA Repair HP precursor powder and their influence to hydration performance. Material and methods Un-hydrated precursor material was characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), X-ray fluorescence (XRF), laser diffraction (LD), N2 physisorption and field emission gun scanning electron microscopy (FEG-SEM). Setting time was assessed according to ASTM specification C 266. Hydrated material was analysed by XRD, FT-IR, energy dispersive X-ray (EDX) analysis and FEG-SEM. Results Ca3SiO5 and Ca2SiO4, in addition to CaWO4 as radiopacifier are the main compositional phase…

CementMaterials scienceScanning electron microscopeResearchchemistry.chemical_elementNanoparticle030206 dentistry02 engineering and technology:CIENCIAS MÉDICAS [UNESCO]021001 nanoscience & nanotechnologyOperative Dentistry and Endodontics03 medical and health sciences0302 clinical medicinechemistryPhysisorptionChemical engineeringAluminiumSpecific surface areaUNESCO::CIENCIAS MÉDICASFourier transform infrared spectroscopy0210 nano-technologyField emission gunGeneral DentistryJournal of Clinical and Experimental Dentistry
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Saturated Solutions of Anhydrous Phases in the System Lime-Silica-Water: Example of beta-C2S

1990

Saturated solutions rerely form when the anhydrous constituents of aluminous and portland cement are stirred in water or in lime solutions of increasing concentrations. Apart from monocalcium aluminate, concentration of ions in solution cannot exceed maximum supersaturation with respect to the hydrate most likely to precipitate. The present work shows such a behavior for β-C2S suspended in water and in lime solutions at low concentration. In more concentrated lime solutions, a short lifetime saturation state with respect to β-C2S seems to be reached.

CementSupersaturationMaterials scienceMineralogyengineering.materiallaw.inventionPortland cementchemistry.chemical_compoundChemical engineeringchemistrylawMonocalcium aluminateMaterials ChemistryCeramics and CompositesengineeringAnhydrousHydrateSaturation (chemistry)LimeJournal of the American Ceramic Society
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Comparison of simultaneous saccharification and fermentation and separate hydrolysis and fermentation processes for butanol production from rice straw

2020

Abstract Rice straw (RS) is one of the lignocellulosic wastes with the highest global production. The main objective of this study was to maximise the butanol production by Clostridium beijerinckii DSM 6422 from RS pretreated by microwave-assisted hydrothermolysis. Two different fermentation strategies were compared: separate hydrolysis and fermentation (SHF, two-step process) and simultaneous saccharification and fermentation (SSF, one-step process). In parallel, the variables that significantly affected the butanol production were screened by using fractional factorial designs. Butanol concentration and productivity at 48 h were, respectively, 8% and 173% higher in SSF than in SHF. A one-…

Central composite designbiologyChemistry020209 energyGeneral Chemical EngineeringButanolOrganic ChemistryEnergy Engineering and Power TechnologyFractional factorial design02 engineering and technologybiology.organism_classificationPulp and paper industryHydrolysischemistry.chemical_compoundFuel TechnologyClostridium beijerinckii020401 chemical engineering0202 electrical engineering electronic engineering information engineeringYeast extractFermentationResponse surface methodology0204 chemical engineeringFuel
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Evolution of Free Volumes in Polycrystalline BaGa2O4 Ceramics Doped with Eu3+ Ions

2021

H.K. and Y.K. would like to thank A. Ingram for assistance in PAL experiments. The authors thank E.A. Kotomin and M. Brik for the many useful discussions. The research was (partly) performed in the Institute of Solid State Physics, University of Latvia ISSP UL. ISSP UL as the Center of Excellence is supported through the Framework Program for European universities Union Horizon 2020, H2020-WIDESPREAD-01–2016–2017-TeamingPhase2 under Grant Agreement No. 739508, CAMART2 project.

CeramicsGeneral Chemical EngineeringFree-volume defects02 engineering and technologydopingceramics01 natural sciencesInorganic ChemistryFragmentationfragmentation0103 physical sciencesceramics; doping; free-volume defects; positron annihilation; agglomeration; fragmentationDopingGeneral Materials Science010302 applied physicsagglomerationCrystallographyAgglomerationPositron annihilationpositron annihilationfree-volume defects021001 nanoscience & nanotechnologyCondensed Matter PhysicsQD901-999:NATURAL SCIENCES [Research Subject Categories]0210 nano-technologyCrystals
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Impact of Thermal Treatment on the Surface of Na0.5Bi0.5TiO3-Based Ceramics

2021

This research was funded by the European Regional Development Fund, grant number 1.1.1.2/VIAA/3/19/558. The Institute of Solid State Physics, University of Latvia as the Center of Excellence has received funding from the European Union’s Horizon 2020 Framework Programme, grant number 739508.

CeramicsMaterials scienceGeneral Chemical EngineeringmicrostructureEvaporation02 engineering and technologyThermal treatmentceramicsSodium bismuth titanate010402 general chemistry01 natural sciencesInorganic Chemistrychemistry.chemical_compoundEtchingThermaletchingGeneral Materials ScienceThermal treatmentCeramicComposite materialMicrostructureCrystallography021001 nanoscience & nanotechnologyCondensed Matter PhysicsMicrostructure0104 chemical sciencesSodium bismuth titanatechemistryEtchingQD901-999visual_artParticle-size distributionvisual_art.visual_art_mediumsodium bismuth titanate:NATURAL SCIENCES [Research Subject Categories]0210 nano-technologythermal treatmentCrystals
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