Search results for "ionic"

showing 10 items of 2016 documents

Geochemistry of REE, Zr and HF in a wide range of pH and water composition: The Nevado del Ruiz volcano hydrothermal system (Colombia)

2015

International audience; The geochemical behaviour of Rare Earth Elements, Zr and Hf was investigated in the thermal waters of Nevado del Ruiz volcano system. A wide range of pH, between 1.0 and 8.8, characterizes these fluids. The acidic waters are sulphate dominated with different Cl/SO4 ratios. The important role of the pH and the ionic complexes for the distribution of REE, Zr and Hf in the aqueous phase was evidenced. The pH rules the precipitation of authigenic Fe and Al oxyhydroxides producing changes in REE, Zr, Hf amounts and strong anomalies of Cerium. The precipitation of alunite and jarosite removes LREE from the solution, changing the REE distribution in acidic waters.Y–Ho and Z…

Acidic waterGeochemistrychemistry.chemical_element[SDU.STU]Sciences of the Universe [physics]/Earth SciencesFractionationengineering.materialHydrothermal circulationGeochemistry and PetrologyRare earth elementJarositeIonic complexeZirconiumFe-Al oxyhydroxideAcidic waters; Fe-Al oxyhydroxides; Hafnium; Ionic complexes; Rare earth elements; Zirconium; Geochemistry and Petrology; GeologyGeologyYttriumAuthigenicAlunite6. Clean waterCeriumchemistry13. Climate actionengineeringZirconiumHafniumGeology
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The modelling of the cathode sheath of an electrical arc in vacuum

2003

This paper presents a simple model of the fragment in the cathode electrical arc root taking into account the physical phenomena occuring on the cathode surface and the sheath. The goal is the obtainment of characteristics values of the heat flux, the electrons, and atoms density in the sheath. Computation is carried out on a one-dimensional model with a coupling between the equation obtained in the sheath and an enthalpy model of the cathode to describe the temperature evolution. In the modelling, we introduce a friction zone above the sheath edge to characterize the heavy particle interactions. Numerical simulation shows that the ionic friction phenomenon deriving from ion–atom collision …

Acoustics and UltrasonicsvacuumIonic bondingarc rootheat fluxElectroncathode sheatharc01 natural sciences010305 fluids & plasmaslaw.inventionElectric arcCross section (physics)lawPhysics::Plasma Physics[PHYS.PHYS.PHYS-PLASM-PH]Physics [physics]/Physics [physics]/Plasma Physics [physics.plasm-ph]0103 physical sciences010306 general physicsCouplingComputer simulationChemistryMechanics[ PHYS.PHYS.PHYS-PLASM-PH ] Physics [physics]/Physics [physics]/Plasma Physics [physics.plasm-ph]Condensed Matter PhysicsCathodeSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsHeat flux
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SOLID LIPID NANOPARTICLES FOR APPLICATIONS IN GENE THERAPY: A REVIEW OF THE STATE OF THE ART

2010

Importance of the field. Gene therapy represents a new paradigm in the prevention and treatment of many inherited and acquired diseases, including genetic disorders, such as cystic fibrosis, haemophilia and many somatic diseases, such as tumours, neurodegenerative diseases and viral infections, such as AIDS. Areas covered in this review. Among a large array of non-viral transfection agents used for in-vitro applications, cationic SLNs are the topic of this review, being recently proposed as an alternative carrier for DNA delivery, due to many technological advantages such as large-scale production from substances generally recognized as safe, good storage stability and possibility of steam …

Acquired diseasesGenetic enhancementGenetic VectorsPharmaceutical ScienceGene deliveryBiologyBioinformaticsCystic fibrosisGenetic therapyGENE THERAPY SOLID LIPID NANOPARTICLESSolid lipid nanoparticlemedicinegene deliverybusiness.industrynon-viral vectors Read More: http://informahealthcare.com/doi/abs/10.1517/17425240903362410DNAGenetic Therapymedicine.diseasegene therapyLipidsBiotechnologySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoMicroscopy Electron ScanningNanoparticlesbusinesscationic solid lipid nanoparticles
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Anionic Polymerization of (Meth)acrylates in the Presence of Cesium Halide−Trialkylaluminum Complexes in Toluene

2001

The polymerization of methyl methacrylate and various acrylates initiated by ester enolates in the presence of cesium halide-trialkylaluminum complexes, Cs[Al n R 2n X] (n = 1, 2; R = Et, Bu'), in toluene has living and controlled character at -20 °C for methacrylates (X = Cl) and at -65 °C for n-butyl acrylate (X = F). Quantitative monomer conversions are usually reached, leading to polymers with narrow molecular weight distributions (M w /M n < 1.1). Kinetic investigations indicate a rather complex polymerization mechanism, and we assume an equilibrium between at least two active species. With this new initiating system, beside acrylate homopolymers, random and graft copolymers can be syn…

Acrylate polymerAcrylatePolymers and PlasticsOrganic ChemistrySolution polymerizationInorganic Chemistrychemistry.chemical_compoundMonomerAnionic addition polymerizationchemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerMethyl methacrylateMacromolecules
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Cast multibilayer films from polymerizable lipids

1987

Acrylate polymerPolymers and PlasticsChemistryScanning electron microscopeOrganic ChemistryAnalytical chemistryInorganic Chemistrychemistry.chemical_compoundMembranePhotopolymerChemical engineeringMaterials ChemistryIonic conductivityReverse osmosisUltraviolet radiationMacromolecules
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Mechanism of Anionic Polymerization of (Meth)acrylates in the Presence of Aluminum Alkyls, 6. Polymerization of Primary and Tertiary Acrylates

1998

The kinetics of the polymerization of n-butyl acrylate initiated by lithiated ester enolates in the presence of aluminum alkyls was investigated in toluene and in toluene/Lewis base mixed solvents at −78 °C. In pure toluene, curved time−conversion plots, incomplete monomer conversion, and broad molecular weight distributions (Mw/Mn ≈ 2) are observedin the absence of aluminum alkyls the molecular weight distributions are significantly broader (Mw/Mn > 14). High monomer conversions and narrower molecular weight distributions (Mw/Mn ≈ 1.5) are obtained when using Lewis bases (e.g., methyl pivalate) as cosolvents. The polymerization of tert-butyl acrylate rapidly reaches full monomer conversion…

AcrylatePolymers and PlasticsOrganic ChemistrySolution polymerizationTolueneInorganic Chemistrychemistry.chemical_compoundMonomerAnionic addition polymerizationPolymerizationchemistryPolymer chemistryMaterials ChemistryMolar mass distributionLewis acids and basesMacromolecules
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Synthesis and solution properties of star-shaped poly(tert-butyl acrylate)

2000

A series of star polymers consisting of poly(tert-butyl acrylate) arms and an ethyleneglycol dimethacrylate (EGDMA) microgel core were synthesized using anionic polymerization. The effect of various parameters (precursor length, ratio [[EGDMA]/[Initiator], reaction time, and overall concentrations) on the average number of arms was investigated. Molecular weights were determined using GPC coupled with an online viscometer and MALLS. The exponents for the relation between intrinsic viscosity or radius of gyration and molecular weight, respectively, are extremely low, indicating that the dimensions of the star polymers only slightly increase with the number of arms. After a certain number of …

AcrylateTert-butyl acrylateMaterials sciencePolymers and PlasticsMolecular massIntrinsic viscosityOrganic ChemistryViscometerStar (graph theory)Condensed Matter PhysicsCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundAnionic addition polymerizationchemistryPolymer chemistryMaterials ChemistryRadius of gyrationPhysical chemistryAstrophysics::Galaxy AstrophysicsMacromolecular Symposia
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1993

The influence of lithium tert-butoxide (tBuOLi) and of lithium chloride on the oligomerization of tert-butyl acrylate (tBuA) initiated by tert-butyl α-lithioisobutyrate (tBiB-Li) was investigated. These additives affect both the kinetics and the product distribution. Whereas the addition of LiCl leads to a narrower molecular-weight distribution (MWD) the presence of tBuOLi induces broader MWD's, characterized by a very high fraction of the dimer. Both additives decrease the rates of propagation to different degrees. These effects are discussed on the basis of the formation of aggregates and adducts, the lithiated dimer having a higher tendency to form aggregates than the other oligomers. Th…

Acrylatechemistry.chemical_compoundAnionic addition polymerizationchemistryDimerPolymer chemistryKineticsAlkoxideLithium chloridechemistry.chemical_elementSolution polymerizationLithiumDie Makromolekulare Chemie
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Potential of phosphonium-based ionic liquids to purify 1-propanol from water by liquid–liquid extraction at mild conditions

2022

Abstract In order to reduce the environmental of the separation of 1-propanol from water in a residual industry stream for its reuse, the capability as solvents of two different trihexyl(tetradecyl)phosphonium ionic liquids (ILs) – trihexyl(tetradecyl)phosphonium chloride ([TDTHP][Cl]) and trihexyl(tetradecyl)phosphonium bromide ([TDTHP][Br])-, was studied. The liquid–liquid equilibria data for both ternary systems, {water + 1-propanol + [TDTHP][Cl]} and {water + 1-propanol + [TDTHP][Br]} at different mild work temperatures, (283.2, 303.2 and 323.2) K, and atmospheric pressure were measured. The thermodynamic parameters for both ternary systems at different work conditions were obtained by …

Activity coefficientChemistryAtomic and Molecular Physics and Opticschemistry.chemical_compoundBromideLiquid–liquid extractionIonic liquidNon-random two-liquid modelPhysical chemistryGeneral Materials SciencePhosphoniumPhysical and Theoretical ChemistrySolubilityTernary operationThe Journal of Chemical Thermodynamics
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Modeling S-carboxymethyl-L-cysteine protonation and activity coefficients in sodium and tetramethylammonium chloride aqueous solutions by SIT and Pit…

2007

Solubility and acid–base properties of S-carboxymethyl-l-cysteine (carbocysteine, ccys) in NaClaq and tetramethylammonium chloride, (CH3)4NClaq ,a tt =2 5 ◦ C and at different ionic strengths were investigated. Solubility was studied at 1.0 ≤ I (mol L −1 ) ≤ 5.0 for NaClaq and 1.0 ≤ I (mol L −1 ) ≤ 3.0 for (CH3)4NClaq, while potentiometric measurements (by ISE-H + , glass electrode) were performed at 0.1 ≤ I (mol L −1 ) ≤ 5.0 for NaClaq and 0.5 ≤ I (mol L −1 ) ≤ 3.0 for (CH3)4NClaq. Solubility data allowed us to determine Setschenow constants and activity coefficients of neutral carbocysteine (H2ccys). Dependence on ionic strength and ionic medium of protonation constants and activity coeff…

Activity coefficientChemistryGeneral Chemical EngineeringPotentiometric titrationInorganic chemistryAnalytical chemistryGeneral Physics and AstronomyProtonationchemistry.chemical_compoundSpecific ion interaction theoryIonic strengthTetramethylammonium chloridePitzer equationsPhysical and Theoretical ChemistrySolubilityCarbocysteine; Solubility; Protonation; Activity coefficients; Dependence on medium and ionic strength
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