Search results for "aqueous solution"

showing 10 items of 1610 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
researchProduct

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
researchProduct

Development of new centrifuges for fast solvent extraction of transactinide elements

1995

The H-0.3 liquid-liquid centrifuge applied for rapid and efficient separation of two liquid phases, and the HG-0.1 gas-liquid centrifuge used to separate the gas phase stemming from a gas jet transportation system and the liquid phase, have been further improved. New centrifuges have been produced of PEEK, a plastic material, which makes them resistant to most aqueous and organic solutions. The performance with respect to time behavior and phase purity is comparable to the titanium centrifuges used so far. The H-0.3 centrifuge has been applied to solvent extraction studies of Zr, Nb, Mo, Hf, Ta, W and Pa from HF solutions into tri-n-octylamine.

CentrifugeJet (fluid)Aqueous solutionChemistryHealth Toxicology and MutagenesisInorganic chemistryPublic Health Environmental and Occupational HealthAnalytical chemistryTransactinide elementchemistry.chemical_elementPollutionAnalytical ChemistryNuclear Energy and EngineeringLiquid–liquid extractionPeekRadiology Nuclear Medicine and imagingSolvent extractionSpectroscopyTitaniumJournal of Radioanalytical and Nuclear Chemistry Articles
researchProduct

Negative-pressure cavitation coupled with aqueous two-phase extraction and enrichment of flavonoids and stilbenes from the pigeon pea leaves and the …

2015

Abstract An efficient extraction method, negative-pressure cavitation coupled with aqueous two-phase extraction (NPC-ATPE), was developed to simultaneously extract and enrich flavonoids and stilbenes from pigeon pea leaves. The main bioactive compounds, cajaninstilbene acid (CSA), longistyline C (LLC), pinostrobin (PI) and pinostrobin chalcone (PIC) were chosen as target compounds. The extraction conditions were optimized using central composite design combined with response surface methodology. The optimized conditions were: concentration of (NH 4 ) 2 SO 4 21% (w/w), concentration of ethanol 23% (w/w) and temperature 30 °C, negative pressure −0.06 MPa, extraction time 30 min and the liquid…

ChalconeAntioxidantAqueous solutionChromatographyABTSCentral composite designDPPHmedicine.medical_treatmentExtraction (chemistry)Filtration and SeparationAnalytical Chemistrychemistry.chemical_compoundchemistrymedicineResponse surface methodologySeparation and Purification Technology
researchProduct

Extraction of uranyl ions from aqueous solutions using silica-gel-bound macrocycles for alpha contaminated waste water treatment

2004

Abstract The efficiency for the extraction of U(VI) of new modified silica gels, namely N-tripropionate (or N-triacetate)-substituted tetraazamacrocycles-bound silica gels, has been studied. The effect of the nature of the ligand, the pH and the temperature was studied both in batch experiments as well as in continuous extraction. These silica gels are good candidates for the extraction of U(VI) when compared to a commercially available acid-type chelating resin. The breakthrough and regeneration tests showed that the total removal of U(VI) from a contaminated solution can be achieved by using a column packed with such tetraazamacrocycles-bound silica gels. Finally, the use of a modified si…

Chelating resinAqueous solutionSilica gelExtraction (chemistry)chemistry.chemical_elementAmericiumUraniumUranylBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryEnvironmental ChemistrySolid phase extractionSpectroscopyNuclear chemistryAnalytica Chimica Acta
researchProduct

Speciation of Al3+ in fairly concentrated solutions (20 to 200 mmol L-1) at I = 1 mol L-1 (NaNO3), in the acidic pH range, at different temperatures.

2011

AbstractThe hydrolysis of Al3+ was studied in aqueous 1 mol L−1 NaNO3 solution at different concentrations (20–200 mmol L−1) and temperatures (283.15–343.15 K) by potentiometry (ISE-H+, glass electrode). Many different speciation models were considered in the calculations and it was found that the best model is represented by the following species: Al(OH)2+, Al(OH)45+, Al13(OH)327+. Hydrolysis constants and enthalpy changes at different temperatures are reported.

Chemical Health and SafetyAqueous solutionChemistryHealth Toxicology and Mutagenesismedia_common.quotation_subjectEnthalpyInorganic chemistryToxicologyGlass electrodelaw.inventionSpeciationHydrolysislawMolePh rangealuminium(III) speciation hydrolysis constants hydrolysis enthalpy changesSettore CHIM/01 - Chimica Analiticamedia_commonAluminium(III) speciation; Hydrolysis constants; Hydrolysis enthalpy changes
researchProduct

Speciation of chitosan with low and high molecular weight carboxylates in aqueous solution

2009

Quantitative data on the speciation of chitosan (310 kDa) with low and high molecular weight carboxylates in aqueous solution are reported. The following carboxylic ligands were considered: monocarboxylate (butyrate); dicarboxylates (malonate, succinate, azelate); tricarboxylate (1,2,3-propa- netricarboxylate); tetracarboxylate (1,2,3,4-butanetetracarboxylate); polyacrylates (2.0 and 20 kDa); polymethacrylate (5.4 kDa). The investigation was performed by potentiometry at t 1/4 25 C, at low ionic strength (without addition of supporting electrolyte) and at I 1/4 0:15 mol L 1 (NaCl). For all the systems the formation of (chitosan)LHi species was found (L 1/4 carboxylic ligand; i 1/4 1 to 4 de…

Chemical Health and SafetyAqueous solutionpolyammonium-polycarboxylate interactionsSupporting electrolyteLigandHealth Toxicology and MutagenesisInorganic chemistrychitosan; polyammonium-polycarboxylate interactions; Chemical speciation; sequestration; effect of ionic strength on sequestrationsequestrationToxicologyTricarboxylateMedicinal chemistrychitosan polyammonium polycarboxylate speciation sequestration ionic strenght.Chitosanchemistry.chemical_compoundMalonatechemistryIonic strengthChemical speciationSettore CHIM/01 - Chimica Analiticaeffect of ionic strength on sequestrationCarboxylatechitosanChemical Speciation & Bioavailability
researchProduct

On the role of interfacial hydrogen bonds in "on-water" catalysis.

2014

Numerous experiments have demonstrated that many classes of organic reactions exhibit increased reaction rates when performed in heterogeneous water emulsions. Despite enormous practical importance of the observed "on-water" catalytic effect and several mechanistic studies, its microscopic origins remains unclear. In this work, the second generation Car-Parrinello molecular dynamics method is extended to self-consistent charge density-functional based tight-binding in order to study "on-water" catalysis of the Diels-Alder reaction between dimethyl azodicarboxylate and quadricyclane. We find that the stabilization of the transition state by dangling hydrogen bonds exposed at the aqueous inte…

Chemical Physics (physics.chem-ph)Aqueous solutionHydrogen bondGeneral Physics and AstronomyFOS: Physical sciencesCondensed Matter - Soft Condensed MatterPhotochemistryCatalysisReaction rateMolecular dynamicschemistry.chemical_compoundchemistryOrganic reactionBiological Physics (physics.bio-ph)Physics - Chemical PhysicsSoft Condensed Matter (cond-mat.soft)Density functional theoryPhysics - Biological PhysicsPhysical and Theoretical ChemistryQuadricyclaneThe Journal of chemical physics
researchProduct

Book Review: Ions in Solution: Basic Principles of Chemical Interactions. By J. Burgess

1989

Chemical engineeringComputational chemistryChemistryMetal ions in aqueous solutionGeneral MedicineGeneral ChemistryChemical interactionCatalysisAngewandte Chemie International Edition in English
researchProduct

Electrochemical characterization of solid state reaction kinetics using voltammetry of microparticles. Application to thermal decomposition of iron c…

2011

The voltammetry of microparticles is applied to characterize the electrocatalytic ability of solids towards selected electrochemical processes. The variation of catalytic currents under fixed electrochemical conditions permits to obtain composition/time data to be fitted with solid state kinetic models. This methodology is applied to analyze the thermal decomposition of magnesiochromite ferroan and chlorite chromian standards and a South Africa iron chromite ore on the basis of the significant catalytic effect on the electrochemical oxygen evolution reaction (OER) in aqueous alkaline media at mineral-modified graphite electrodes. Measurement of the time variation of catalytic current for OE…

Chemical kineticsAqueous solutionChemistryThermal decompositionInorganic chemistryMaterials ChemistryOxygen evolutionGeneral ChemistryChromiteElectrochemistryVoltammetryCatalysisJournal of Materials Chemistry
researchProduct