Search results for "Chemical engineering"

showing 10 items of 5892 documents

Lineage-reprogramming of Pericyte-derived Cells of the Adult Human Brain into Induced Neurons

2014

Direct lineage-reprogramming of non-neuronal cells into induced neurons (iNs) may provide insights into the molecular mechanisms underlying neurogenesis and enable new strategies for in vitro modeling or repairing the diseased brain. Identifying brain-resident non-neuronal cell types amenable to direct conversion into iNs might allow for launching such an approach in situ, i.e. within the damaged brain tissue. Here we describe a protocol developed in the attempt of identifying cells derived from the adult human brain that fulfill this premise. This protocol involves: (1) the culturing of human cells from the cerebral cortex obtained from adult human brain biopsies; (2) the in vitro expansio…

Cell typePatch-Clamp TechniquesGeneral Chemical EngineeringCell Culture TechniquesBiologyGeneral Biochemistry Genetics and Molecular BiologySOX2Transduction GeneticmedicineHumansCell LineageCerebral CortexNeuronsGeneral Immunology and MicrobiologyGeneral NeuroscienceSOXB1 Transcription FactorsNeurogenesisHuman brainCell sortingCellular ReprogrammingFlow CytometryImmunohistochemistrymedicine.anatomical_structureRetroviridaeCell culturePericytePericytesNeuroscienceReprogrammingNeuroscience
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Mechanisms of cement hydration

2011

Abstract The current state of knowledge of cement hydration mechanisms is reviewed, including the origin of the period of slow reaction in alite and cement, the nature of the acceleration period, the role of calcium sulfate in modifying the reaction rate of tricalcium aluminate, the interactions of silicates and aluminates, and the kinetics of the deceleration period. In addition, several remaining controversies or gaps in understanding are identified, such as the nature and influence on kinetics of an early surface hydrate, the mechanistic origin of the beginning of the acceleration period, the manner in which microscopic growth processes lead to the characteristic morphologies of hydratio…

CementAliteMaterials scienceDiffusionInduction period0211 other engineering and technologiesMineralogy02 engineering and technologyBuilding and Construction021001 nanoscience & nanotechnologylaw.inventionReaction ratechemistry.chemical_compoundPortland cementchemistryChemical engineeringlaw021105 building & constructionGeneral Materials ScienceTricalcium aluminate0210 nano-technologyHydrateCement and Concrete Research
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Characterization by solid-state NMR and selective dissolution techniques of anhydrous and hydrated CEM V cement pastes.

2010

International audience; The long term behaviour of cement based materials is strongly dependent on the paste microstructure and also on the internal chemistry. A CEM V blended cement containing pulverised fly ash (PFA) and blastfurnace slag (BFS) has been studied in order to understand hydration processes which influence the paste microstructure. Solid-state NMR spectroscopy with complementary X-ray diffraction analysis and selective dissolution techniques have been used for the characterization of the various phases (C3S, C2S, C3A and C4AF) of the clinker and additives and then for estimation of the degree of hydration of these same phases. Their quantification after simulation of experime…

CementBlended cement (D)Materials science0211 other engineering and technologiesSlagMineralogy02 engineering and technologyBuilding and ConstructionNuclear magnetic resonance spectroscopy021001 nanoscience & nanotechnologyMicrostructureClinker (cement)NMR spectroscopyChemical engineeringGround granulated blast-furnace slagvisual_artFly ash021105 building & constructionvisual_art.visual_art_mediumHydration (A)General Materials ScienceAmorphous material (B)0210 nano-technologyDissolution
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Effect of blastfurnace slag addition to Portland cement for cationic exchange resins encapsulation

2013

In the nuclear industry, cement-based materials are extensively used to encapsulate spent ion exchange resins (IERs) before their final disposal in a repository. It is well known that the cement has to be carefully selected to prevent any deleterious expansion of the solidified waste form, but the reasons for this possible expansion are not clearly established. This work aims at filling the gap. The swelling pressure of IERs is first investigated as a function of ions exchange and ionic strength. It is shown that pressures of a few tenths of MPa can be produced by decreases in the ionic strength of the bulk solution, or by ion exchanges (2Na + instead of Ca 2+ , Na + instead of K + ). Then,…

CementCationic exchangeMaterials sciencePhysicsQC1-999Cationic polymerizationSwelling pressureMineralogyIonlaw.inventionPortland cementChemical engineeringlawIonic strengthIon-exchange resinEPJ Web of Conferences
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Hydration Chemistry of Cement Studied by Near Infrared Spectroscopy

2018

Cement is a complex mixture of inorganic compounds which mainly composed of calcium silicates and calcium aluminates. Cement is mixed with water to form concrete. During the mixing calcium silicate hydrate (CSH) and calcium hydroxide are formed. The ratio of water/cement (w/c ratio) is important to obtain a mixture that gives optimum strength to the concrete. In this work, three different cement samples were mixed with water in four different ratios, including 0.35, 0.40, 0.45 and 0.55, respectively. The hydration process of cement was investigated by using near infrared (NIR) spectroscopy over a period of 28 days. The combination frequency of OH stretching and bending of water molecules gi…

CementChemical engineeringMechanics of MaterialsChemistryMechanical Engineering0206 medical engineeringNear-infrared spectroscopyGeneral Materials Science02 engineering and technology021001 nanoscience & nanotechnology0210 nano-technology020601 biomedical engineering
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Studies on mechanism and physico-chemical parameters at the origin of the cement setting. I. The fundamental processes involved during the cement set…

1995

Abstract The mechanical evolution and the structure of the cement paste have been analysed in relation with the chemical evolution of the system. The setting process can be described as following 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 hydrates formation During the coagulation step, the structure formed is proved to be mechanically reversible. The rigidification of the coagulated structure is provided by the hydrates formation in the contact zone. The increase of the paste cohesion at this stage is proportional to the quan…

CementChemical evolutionMaterials scienceChemical engineeringMixing (process engineering)Coagulation (water treatment)Contact zoneMineralogyGeneral Materials ScienceBuilding and ConstructionCement pasteCement and Concrete Research
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Importance of the liquid to solid weight ratio in the powdered solid-liquid reactions Example drawn from cement constituent hydration

1997

Abstract It seems justified to wonder if the chemical processes which have been evidenced from diluted stirred suspensions are or are not in accordance with those involved in a stagnant paste. The present paper is aimed at clarifying this question which is in connection with the problem of the so called ‘dormant period’ or ‘induction period’ at the beginning of the hydration of Portland cement.

CementChemistryInduction periodMineralogyGeneral ChemistryCondensed Matter PhysicsSuspension (chemistry)law.inventionPortland cementChemical reaction kineticsChemical engineeringlawSpecific surface areaGeneral Materials ScienceSolid liquidSolid State Ionics
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Electrokinetic Properties which Control the Coagulation of Silicate Cement Suspensions during Early Age Hydration

1998

The coagulation of cement particles during early age hydration has been previously identified as the first step of the setting and hardening of cement pastes. By hydrating Ca3SiO5and a silicate-rich clinker under controlled conditions, a correlation between the coagulation of the suspensions and the electrokinetic properties of particles is established. The zeta potential, and hence the surface charge, of particles in suspension depends on the calcium content of the medium. At low concentrations of Ca2+, the zeta potential of Ca3SiO5particles, calcium silicate hydrate (C–S–H), and clinker is negative (<−30 mV) and the suspensions are well dispersed. A strong coagulation occurs at intermedia…

CementChemistryMineralogySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundElectrokinetic phenomenaColloid and Surface ChemistryChemical engineeringParticle-size distributionHardening (metallurgy)Zeta potentialSilicate CementSurface chargeCalcium silicate hydrateJournal of Colloid and Interface Science
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Surface Relaxivity of Cement Hydrates

2014

Numerous aspects of the physical chemistry of colloidal systems are conditioned by the solid–liquid interface, and this is also the case for hydrated cement systems. Estimating the surface area is thus essential for studying the kinetics of cement hydration and admixture adsorption. Proton nuclear magnetic resonance (NMR) relaxation techniques have already proven useful for this objective, but, for hydrating cements at early ages, it is necessary to know the surface relaxivities of all of the individual phases present to correctly interpret the relaxation data. This paper reports the results of a comparison of NMR relaxometry and Brunauer–Emmett–Teller gas adsorption measurements on various…

CementEttringiteRelaxometryMaterials scienceRelaxation (NMR)Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsColloidchemistry.chemical_compoundParamagnetismGeneral EnergyAdsorptionChemical engineeringchemistryProton NMRPhysical and Theoretical ChemistryThe Journal of Physical Chemistry C
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Hydration of alite containing aluminium

2011

Abstract The most important phase in Portland cement is tricalcium silicate, which leads during its hydration to the nucleation and growth of calcium silicate hydrate [referred to as C–S–H, (CaO)x–SiO2–(H2O)y]. The development of this hydrate around the cement grains is responsible for the setting and hardening of cement pastes. The general term for designating the tricalcium silicate in cements is alite. This name relates to all polymorphs containing various foreign ions inserted in their structure. These ions may influence the intrinsic reactivity, and once released during the dissolution, they may interact also with C–S–H. One of the most likely species to be inserted in the alite struct…

CementMaterials scienceAliteNucleationMineralogychemistry.chemical_elementIndustrial and Manufacturing Engineeringlaw.inventionPortland cementchemistry.chemical_compoundchemistryChemical engineeringlawAluminiumCeramics and CompositesCalcium silicate hydrateHydrateDissolutionAdvances in Applied Ceramics
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