Search results for "Chloride"

showing 10 items of 1691 documents

Revisited Dual Luminescence of 2,2′-Dipyridylamine Hydrochloride in Solution and Physical Processes behind It

2018

hydrogen bondamiinitliuoksetChemistryHydrochlorideprotonationfluoresenssi22'-dipyridylamine02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistrysuolahappo01 natural sciences0104 chemical sciencesabsorptiochemistry.chemical_compoundluminescence0210 nano-technologyLuminescenceta116absorptionChemistrySelect
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Salt release monitoring with specific sensors in "in vitro" oral and digestive environments from soft cheeses

2012

International audience; The objective of the present work is to demonstrate the interest and the feasibility of the measurement of NaCl concentrations in soft cheeses and in particular an in vitro digestion process by the use of chemical sensors. The analyzed matrices were the commercial Italian mozzarella cheeses and domestic cheese base models. The classification of mozzarellas was performed according to their salinity, while the breakdown of cheese base models has been followed both at initial steps of digestion in artificial mouth dispositive mimicking the oral sphere and in a gut-imitating digester (TIM-1). During the breakdown of soft cheese in the digester, the estimated values for N…

in vitro digestion processBase (chemistry)SodiumAnalytical chemistrySalt (chemistry)chemistry.chemical_elementSodium Chloridein vitro mouth processSodium detectionSettore ING-INF/01 - Elettronica01 natural sciencesChlorideChemistry Techniques AnalyticalAnalytical ChemistrySoft cheesesSalt release0404 agricultural biotechnologyBiomimetics[SDV.IDA]Life Sciences [q-bio]/Food engineeringCalibrationmedicine[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process EngineeringIntestinal MucosaSensor arraychemistry.chemical_classificationMouthChromatographyIonic chromatographySettore CHIM/07 - Fondamenti Chimici delle Tecnologie010401 analytical chemistry04 agricultural and veterinary sciences040401 food science0104 chemical sciencesSalinitychemistrySalt release in vitro mouth process in vitro digestion process Sensor array Sodium detection Soft cheesesDigestionDairy ProductsDigestionmedicine.drug
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Inhibitoren der Korrosion 25(1) - Über die Rolle der Kationen in Neutralsalzen bei der Korrosion von Eisenwerkstoffen in Gegenwart von Sauerstoff

1979

Die Geschwindigkeit des Sauerstoffverbrauchs bei der Korrosion von jeweils 500 mg DAB6-Eisenpulver wird in Abhangigkeit von der Art des Kations in Neutralsalzen (Chloriden) unter Standardbedingungen bestimmt. In Gegenwart von Alkali-, Quartaren Ammonium, Quartaren Phosphonium-und Erdalkalichloriden ist die Geschwindigkeit des Sauerstoffverbrauches vergleichbar gros. Mit Zink-, Cadmium-, Nickel-und Kobaltchloriden wird aber im Bereich von pH5 bis pH7 eine uberraschend grose Verzogerung der Sauerstoffaufnahme beobachtet. Es handelt sich mit hoher Wahrscheinlichkeit um eine Blockade der kathodischen Bezirke in der Eisengrenzflache durch Abscheidung der schwerloslichen basischen Hydroxyde von Z…

inorganic chemicalsCadmiumChemistryMechanical EngineeringMetals and Alloyschemistry.chemical_elementGeneral MedicineZincChlorideOxygenSurfaces Coatings and FilmsNickelchemistry.chemical_compoundMechanics of MaterialsMaterials ChemistrymedicineEnvironmental ChemistryAmmoniumPhosphoniumCobaltmedicine.drugNuclear chemistryMaterials and Corrosion/Werkstoffe und Korrosion
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Vanadium-based Ziegler-Natta catalyst supported on MgCl2(THF)2 for ethylene polymerization

1996

A supported magnesium‐vanadium‐aluminium catalyst was prepared by depositing –with the use of a milling technique–VOCl3 on the MgCl2(THF)2 support and subsequent activation with diethylaluminium chloride. Catalytic activity of the obtained system for ethylene polymerization was evaluated as a function of Mg/V and Al/V ratios as well as catalyst ageing time and polymerization temperature. High concentrations of THF in the catalytic system and considerable excess of an organoaluminium co‐catalyst were found to have no deactivating action on vanadium active sites. The catalyst obtained is stable and its activity for ethylene polymerization is high. It yields polyethylene with higher molecular …

inorganic chemicalsDiethylaluminium chloridePolymers and PlasticsOrganic Chemistrytechnology industry and agricultureVanadiumchemistry.chemical_elementSolution polymerizationPolyethyleneCatalysischemistry.chemical_compoundchemistryPolymerizationPolymer chemistryMaterials ChemistryCoordination polymerizationZiegler–Natta catalystMacromolecular Rapid Communications
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Iron Oxide/Hydroxide Nanoparticles with Negatively Charged Shells Show Increased Uptake in Caco-2 Cells

2012

The absorption of commonly used ferrous iron salts from intestinal segments at neutral to slightly alkaline pH is low, mainly because soluble ferrous iron is easily oxidized to poorly soluble ferric iron and because ferrous iron, but not ferric iron, is carried by the divalent metal transporter DMT-1. Moreover, ferrous iron frequently causes gastrointestinal side effects. Iron hydroxide nanoparticles with neutral and hydrophilic carbohydrate shells are alternatively used to ferrous salts. In these formulations gastrointestinal side effects are rare because hundreds of ferric iron atoms are safely packed in nanoscaled cores surrounded by the solubilizing shell; nevertheless, iron bioavailabi…

inorganic chemicalsInorganic chemistryIron oxidePharmaceutical ScienceIron deficiencymedicine.diseaseFerric CompoundsChlorideFerrouschemistry.chemical_compoundChloridesMicroscopy Electron TransmissionchemistryDrug DiscoverymedicineHumansNanoparticlesMolecular MedicineFerricHydroxideCaco-2 CellsSulfateIron oxide nanoparticlesmedicine.drugMolecular Pharmaceutics
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Crystal structure of the molecular adduct of dimethyltin(IV) chloride with N,N′-ethylenebis(salicylideneiminato) nickel(II)

1974

Abstract N,N′-Ethylenebis(salicylideneiminato)nickel(II) behaves as a neutral bidentate ligand through its oxygen atoms forming binuclear complexes with organotin(IV) chlorides. The crystal structure of the dimethyl derivative is reported.

inorganic chemicalsOrganic ChemistryInorganic chemistrychemistry.chemical_elementCrystal structureBiochemistryChlorideAdductInorganic Chemistrychemistry.chemical_compoundNickelOxygen atomchemistryPolymer chemistryMaterials ChemistrymedicinePhysical and Theoretical ChemistryDerivative (chemistry)medicine.drugJournal of Organometallic Chemistry
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UraniumIV and uranyle salts, efficient and reusable catalysts for acylation of aromatic compounds

2000

Abstract Uranium tetrachloride, uranyle chloride, fluoride and also nitrate or acetate are very efficient homogeneous catalysts for the Friedel–Crafts acylation of aromatic compounds. With uranyle salts, the reaction, carried under dry air, is highly specific and the mono- or bisacylation products are obtained in high yield. Uranyle catalyst can be quantitatively recovered and reused and the organic products are obtained free of uranium.

inorganic chemicalsProcess Chemistry and TechnologyHomogeneous catalysisEtherChlorideCatalysisCatalysisAcylationchemistry.chemical_compoundchemistrymedicineOrganic chemistryPhysical and Theoretical ChemistryUranium tetrachlorideFriedel–Crafts reactionFluorideNuclear chemistrymedicine.drugJournal of Molecular Catalysis A: Chemical
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Nitrous oxide emissions in a membrane bioreactor treating saline wastewater contaminated by hydrocarbons

2016

The joint effect of wastewater salinity and hydrocarbons on nitrous oxide emission was investigated. The membrane bioreactor pilot plant was operated with two phases: i. biomass acclimation by increasing salinity from 10 gNaCl L−1 to 20 gNaCl L−1 (Phase I); ii. hydrocarbons dosing at 20 mg L−1 with a constant salt concentration of 20 gNaCl L−1 (Phase II). The Phase I revealed a relationship between nitrous oxide emissions and salinity. During the end of the Phase I, the activity of nitrifiers started to recover, indicating a partial acclimatization. During the Phase II, the hydrocarbon shock induced a temporary inhibition of the biomass with the suppression of nitrous oxide emissions. The r…

inorganic chemicalsSalinityEnvironmental Engineering0208 environmental biotechnologyBiomassBioengineering02 engineering and technology010501 environmental sciencesSodium ChlorideWastewaterMembrane bioreactor01 natural sciencesWaste Disposal FluidEnvironmental protectionGreenhouse gas emissionchemistry.chemical_compoundBioreactorsBiomassWaste Management and Disposal0105 earth and related environmental scienceschemistry.chemical_classificationNitrous oxideSettore ICAR/03 - Ingegneria Sanitaria-AmbientaleRenewable Energy Sustainability and the EnvironmentChemistryEnvironmental engineeringGeneral MedicineNitrous oxideequipment and suppliesHydrocarbons020801 environmental engineeringSalinity and hydrocarbonSalinityHydrocarbonPilot plantBiodegradation EnvironmentalWastewaterEnvironmental chemistryMembrane bioreactorAerationWater Pollutants ChemicalEnvironmental protection; Greenhouse gas emissions; Membrane bioreactors; Nitrous oxide; Salinity and hydrocarbon; Bioengineering; Environmental Engineering; Waste Management and Disposal
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A DFT study on the NHC catalysed Michael addition of enols to α,β-unsaturated acyl-azoliums. A base catalysed C–C bond-formation step

2013

The NHC catalysed nucleophilic additions of enols to α,β-unsaturated acyl-azolium intermediates have been investigated using DFT methods at the MPWB1K/6-31G** computational level. In the direct and the conjugate additions, formation of a hydrogen bond (HB) with the carboxyl oxygen is not sufficient to favour the C-C bond formation as a consequence of the low nucleophilic character of enols. Interestingly, when enols form a HB with the chloride counterion, the activation energies associated with the conjugate addition decrease as a consequence of the increased nucleophilic character of enols and the increased electrophilic character of the 'acyl-azolium + Cl' ion pair. Analysis of the DFT re…

inorganic chemicalschemistry.chemical_classificationHydrogen bondChemistryStereochemistryOrganic ChemistryBiochemistryChlorideMedicinal chemistryNucleophileElectrophileMichael reactionmedicineReactivity (chemistry)Physical and Theoretical ChemistryCounterionmedicine.drugConjugateOrg. Biomol. Chem.
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Enantioselective transport of amino acid through supported chiral liquid membranes

1993

Abstract Two chiral alcohols, nopol and (2S)-(−)-methyl-1-butanol, immobilized in the pores of a polyethylene film were used for the anantioselective transport of amino acid hydrochloride. The degree of stereoselectivity of the permeation process varied from 0.39 to 1.52 depending on both the type of the chiral membrane phase and the properties of the amino acid. The evaluation of the membrane ability to separate stereoisomers was performed by the step-by-step analysis by considering the effect of amino acids' hydrophobicity, polarity and degree of chirality. For the purpose of this paper, the chirality measure was introduced. It was demonstrated that the enantioselectivity was affected mai…

inorganic chemicalschemistry.chemical_classificationamino acidschiral discriminationStereochemistryHydrochlorideorganic chemicalsEnantioselective synthesisFiltration and SeparationPermeationBiochemistryAmino acidsupported liquid membraneschemistry.chemical_compoundMembranechemistryPhase (matter)Organic chemistryheterocyclic compoundsGeneral Materials ScienceStereoselectivityPhysical and Theoretical ChemistryChirality (chemistry)Journal of Membrane Science
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