Search results for "Hydrate"

showing 10 items of 3383 documents

Geographical mapping of metabolites in biological tissue with quantitative bioluminescence and single photon imaging

1993

This article features a novel technique for measuring the spatial distribution of metabolites, such as ATP, glucose, and lactate, in rapidly frozen tissue. Concentration values are obtained in absolute terms and with a spatial resolution of single-cell dimension. The method is based on enzymatic reactions that link the metabolite of interest to luciferase with subsequent light emission. Using a specific array, cryosections are brought into contact with the enzymes in a well-defined, reproducible way inducing a distribution of light across the section with an intensity that is proportional to the metabolite concentration. The emitted light can be visualized through a microscope and an imagin…

Cell SurvivalMetaboliteUterine Cervical NeoplasmsCarbohydrate metabolismBiologyMiceStructure-Activity Relationshipchemistry.chemical_compoundAdenosine TriphosphateNeoplasmsTumor Cells CulturedAnimalsFrozen SectionsHumansBioluminescenceTissue DistributionLuciferaseLactic AcidMelanomaCells Culturedchemistry.chemical_classificationMice Inbred BALB CStaining and LabelingHistocytochemistryMyocardiumCell BiologyPhoton countingRatsLactic acidGlucoseEnzymechemistryBiochemistryLuminescent MeasurementsLactatesBiophysicsFemaleLight emissionAnatomyThe Histochemical Journal
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α-Secretase Activity of the Disintegrin Metalloprotease ADAM 10: Influences of Domain Structure

2001

Disintegrin metalloproteases from different organisms form the ADAM (a disintegrin and metalloprotease) family. All members display a common domain organization and possess four potential functions: proteolysis, cell adhesion, cell fusion, and cell signaling. Members of the ADAM family are responsible for the proteolytic cleavage of transmembrane proteins and release of their extracellular domain. The proteolytic process is referred to as ectodomain shedding, which is activated by phorbol esters and inhibited by hydroxamic acid-based inhibitors. We have shown that the disintegrin metalloprotease ADAM 10 has both constitutive and regulated alpha-secretase activity. Expression of a dominant n…

Cell signalingDisintegrinsMolecular Sequence DataProtein domainBiologyGeneral Biochemistry Genetics and Molecular BiologyADAM10 ProteinAmyloid beta-Protein PrecursorHistory and Philosophy of ScienceEndopeptidasesDisintegrinAnimalsAspartic Acid EndopeptidasesHumansProtease InhibitorsAmino Acid SequenceCell adhesionMetalloproteinaseGeneral NeuroscienceHEK 293 cellsMembrane ProteinsMetalloendopeptidasesRecombinant ProteinsTransmembrane proteincarbohydrates (lipids)ADAM ProteinsBiochemistryEctodomainbiology.proteinAmyloid Precursor Protein SecretasesProtein Processing Post-TranslationalAnnals of the New York Academy of Sciences
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Multivalency Beats Complexity: A Study on the Cell Uptake of Carbohydrate Functionalized Nanocarriers to Dendritic Cells.

2020

Herein, we report the synthesis of carbohydrate and glycodendron structures for dendritic cell targeting, which were subsequently bound to hydroxyethyl starch (HES) nanocapsules prepared by the inverse miniemulsion technique. The uptake of the carbohydrate-functionalized HES nanocapsules into immature human dendritic cells (hDCs) revealed a strong dependence on the used carbohydrate. A multivalent mannose-terminated dendron was found to be far superior in uptake compared to the structurally more complex oligosaccharides used.

CellcarbohydratesBlood DonorsHydroxyethyl starch010402 general chemistryLigands01 natural sciencesNanocapsulesArticleHydroxyethyl Starch DerivativesDrug Delivery SystemsDendrimermedicineHumanslcsh:QH301-705.5Cells Cultured010405 organic chemistryChemistrynanocapsulesBiological TransportGeneral MedicineDendritic cellDendritic CellsCarbohydrate0104 chemical sciencesMiniemulsionmedicine.anatomical_structurelcsh:Biology (General)BiophysicsglycodendronsNanocarrierscell targetingmedicine.drugCells
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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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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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Prediction of Long-Term Chemical Evolution of a Low-pH Cement Designed for Underground Radioactive Waste Repositories

2012

Low-pH cements, also referred as low-alkalinity cements, are binders with a pore solution pH ≤ 11. They can be designed by replacing significant amounts of Portland cement (OPC) (≥40 %) by silica fume, which can be associated in some cases to low-CaO fly ash and/or ground granulated blast furnace slag to decrease the heat output during hydration by dilution of OPC and improve the mechanical strength of the final material. With the prospect of using these materials in a geological repository, it is of main importance to estimate their long-term properties and the influence of external and internal factors (chemical composition of the binder, storage temperature) on their characteristics. For…

CementEngineeringSilica fumeWaste managementbusiness.industryMetallurgytechnology industry and agricultureengineering.materiallaw.inventionchemistry.chemical_compoundPortland cementchemistryGround granulated blast-furnace slaglawFly ashSlurryCalcium silicate hydratebusinessLime
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Investigation of magnesium phosphate cement hydration in diluted suspension and its retardation by boric acid

2016

Abstract Magnesium phosphate cements (MPCs) are used for rapid repair works, but they may also offer prospects for the stabilization/solidification of deleterious waste. MPCs contain calcined magnesium oxide and a water-soluble acid phosphate, such as potassium dihydrogen phosphate (KH 2 PO 4 ). The main precipitated hydrate is then K-struvite (MgKPO 4 ·6H 2 O). This work aims at giving new insight into the processes involved in its formation. Since cement hydration is very rapid, the second objective is to understand how boric acid, a common admixture for field application, retards cement hydration. A multi-stage process is evidenced in diluted suspension: MgHPO 4 ·7H 2 O likely precipitat…

CementMagnesium phosphateMaterials scienceMagnesiumPotassiumInorganic chemistry0211 other engineering and technologieschemistry.chemical_element02 engineering and technologyBuilding and Construction[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyPhosphateBoric acidchemistry.chemical_compoundchemistry021105 building & construction[CHIM]Chemical SciencesGeneral Materials Science0210 nano-technologyHydrateDissolutionComputingMilieux_MISCELLANEOUS
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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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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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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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