Search results for "Salts"

showing 10 items of 258 documents

Effective Henry's law partitioning and the salting constant of glyoxal in aerosols containing sulfate.

2013

The reversible partitioning of glyoxal was studied in simulation chamber experiments for the first time by time-resolved measurements of gas-phase and particle-phase concentrations in sulfate-containing aerosols. Two complementary methods for the measurement of glyoxal particle-phase concentrations are compared: (1) an offline method utilizing filter sampling of chamber aerosols followed by HPLC-MS/MS analysis and (2) positive matrix factorization (PMF) analysis of aerosol mass spectrometer (AMS) data. Ammonium sulfate (AS) and internally mixed ammonium sulfate/fulvic acid (AS/FA) seed aerosols both show an exponential increase of effective Henry's law coefficients (KH,eff) with AS concentr…

AerosolsAmmonium sulfateMolalityChromatography010504 meteorology & atmospheric sciencesSulfatesAnalytical chemistryGeneral ChemistryGlyoxal010501 environmental sciencesMass spectrometry01 natural sciencesHenry's lawAerosolchemistry.chemical_compoundchemistryIonic strengthTandem Mass SpectrometryEnvironmental ChemistryGlyoxalSaltsSulfateChromatography High Pressure Liquid0105 earth and related environmental sciencesEnvironmental sciencetechnology
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NMR Spectroscopic Evidence for the Intermediacy of XeF3− in XeF2/F− Exchange, Attempted Syntheses and Thermochemistry of XeF3− Salts, and Theoretical…

2010

The existence of the trifluoroxenate(II) anion, XeF(3)(-), had been postulated in a prior NMR study of the exchange between fluoride ion and XeF(2) in CH(3)CN solution. The enthalpy of activation for this exchange, ΔH(⧧), has now been determined by use of single selective inversion (19)F NMR spectroscopy to be 74.1 ± 5.0 kJ mol(-1) (0.18 M) and 56.9 ± 6.7 kJ mol(-1) (0.36 M) for equimolar amounts of [N(CH(3))(4)][F] and XeF(2) in CH(3)CN solvent. Although the XeF(3)(-) anion has been observed in the gas phase, attempts to prepare the Cs(+) and N(CH(3))(4)(+) salts of XeF(3)(-) have been unsuccessful, and are attributed to the low fluoride ion affinity of XeF(2) and fluoride ion solvation in…

AnionsAcetonitrilesMagnetic Resonance SpectroscopyXenonChemistryInorganic chemistrySolvationNuclear magnetic resonance spectroscopyElectron localization functionIonInorganic ChemistryFluoridesCrystallographyMolecular geometryThermochemistryQuantum TheoryThermodynamicsSaltsDensity functional theoryPhysical and Theoretical ChemistryLone pairInorganic Chemistry
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CH-Directed Anion-π Interactions in the Crystals of Pentafluorobenzyl-Substituted Ammonium and Pyridinium Salts

2010

Simple pentafluorobenzyl-substituted ammonium and pyridinium salts with different anions can be easily obtained by treatment of the parent amine or pyridine with the respective pentafluorobenzyl halide. Hexafluorophosphate is introduced as the anion by salt metathesis. In the case of the ammonium salt 4, water co-crystallisation seems to suppress effective anion-pi interactions of bromide with the electron-deficient aromatic system, whereas with salts 5 and 6 such interactions are observed despite the presence of water. However, due to asymmetric hydrogen-bonding interactions with ammonium side chains, the anion of 5 is located close to the rim of the pentafluorophenyl group (eta(1) interac…

AnionsHydrocarbons FluorinatedInorganic chemistryChemieMolecular ConformationSalt (chemistry)Pyridinium CompoundsCrystallography X-RayMedicinal chemistryCatalysischemistry.chemical_compoundBromideHexafluorophosphatePyridineAmmoniumPi interactionchemistry.chemical_classificationMolecular StructureChemistryHydrogen bondOrganic ChemistryHydrogen BondingGeneral ChemistryCarbonQuaternary Ammonium CompoundsModels ChemicalSaltsPyridiniumChemistry - A European Journal
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Recovery of Lithium Carbonate from Dilute Li-Rich Brine via Homogenous and Heterogeneous Precipitation

2022

An extensive experimental campaign on Li recovery from relatively dilute LiCl solutions (i.e., Li+ similar to 4000 ppm) is presented to identify the best operating conditions for a Li2CO3 crystallization unit. Lithium is currently mainly produced via solar evaporation, purification, and precipitation from highly concentrated Li brines located in a few world areas. The process requires large surfaces and long times (18-24 months) to concentrate Li` up to 20,000 ppm. The present work investigates two separation routes to extract Li+ from synthetic solutions, mimicking those obtained from low-content Li+ sources through selective Li+ separation and further concentration steps: (i) addition of …

AnionsIonsSettore ING-IND/26 - Teoria Dello Sviluppo Dei Processi Chimici:Enginyeria química [Àrees temàtiques de la UPC]General Chemical EngineeringMetal recovery Lithium recovery Crystallization Water resourcesSaltsGeneral ChemistryPrecipitationLithiumLitiIndustrial and Manufacturing Engineering
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Anion-Exchange Properties of Trifluoroacetate and Triflate Salts of N-Alkylammonium Resorcinarenes

2016

The synthesis of N-benzyl- and N-cyclohexylammonium resorcinarene trifluoroacetate (TFA) and triflate (OTf) salt receptors was investigated. Solid-state analysis by single-crystal X-ray diffraction revealed that the N-alkylammonium resorcinarene salts (NARSs) with different upper substituents had different cavity sizes and different affinities for anions. Anion-exchange experiments by mixing equimolar amounts of N-benzylammonium resorcinarene trifluoroacetate and N-cyclohexylammonium resorcinarene triflate, as well as N-benzylammonium resorcinarene triflate and N-cyclohexylammonium resorcinarene trifluoroacetate showed that the NARS with flexible benzyl groups preferred the larger OTf anion…

AnionsModels MolecularsaltsPhenylalanineElectrospray ionizationInorganic chemistrySalt (chemistry)Benzylammonium CompoundsCrystallography X-Ray010402 general chemistryCrystal engineeringchemistry01 natural sciencesBiochemistryIonDioxanesX-rayPolymer chemistryTrifluoroacetic AcidAnion bindingta116N-AlkylammoniumMesylateschemistry.chemical_classificationanion-exchangeIon exchange010405 organic chemistryChemistryOrganic ChemistryGeneral ChemistryResorcinarene3. Good health0104 chemical sciencesCalixarenesTrifluoromethanesulfonateChemistry: An Asian Journal
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Alternariol-induced cytotoxicity in Caco-2 cells. Protective effect of the phenolic fraction from virgin olive oil.

2014

The extra virgin olive oil (EVOO) has been associated to antioxidant effects. The mycotoxin alternariol (AOH) can contaminate olives. The aims of this work were to determine the cytotoxic effects and reactive oxygen species (ROS) produced by AOH, tyrosol and oleuropein (two polyphenols of olive oil) and a real EVOO extract in Caco-2 cells. The MTT assay and the ROS production by the H2-DCFDA probe were used. Results demonstrated that AOH reduces cellular proliferation depending on concentration, whereas tyrosol and oleuropein did not (12.5-100 μM). The combination of AOH + oleuropein (50 μM) increased cell proliferation (24%) whereas, AOH + tyrosol decreased (47%) it. Besides, AOH increased…

Antioxidantmedicine.medical_treatmentAlternariolAlternariol; Caco-2 cells; Cytotoxic and cytoprotective effect; Extra virgin olive oil; Phenolic compounds; ROS generationTetrazolium SaltsToxicologychemistry.chemical_compoundLactonesPhenolsOleuropeinExtra virgin olive oilmedicineHumansPlant OilsMTT assayPhenolsOlive OilCell Proliferationchemistry.chemical_classificationReactive oxygen speciesAnalysis of VariancePlant ExtractsPhenolic compoundsTyrosolAlternariolThiazoleschemistryBiochemistryPolyphenolROS generationCaco-2 CellsReactive Oxygen SpeciesCytotoxic and cytoprotective effectToxicon : official journal of the International Society on Toxinology
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Protonation of Carbonate in Aqueous Tetraalkylammonium Salts at 25°C.

2006

Protonation constants of carbonate were determined in tetramethylammonium chloride (Me4NClaq 0.1≤I/mol kg−1 ≤4) and tetraethylammonium iodide (Et4NIaq 0.1≤I/mol kg−1 ≤1) by potentiometric ([H+]-glass electrode) measurements. Dependence of protonation constants on ionic strength was taken into account by modified specific ion interaction theory (SIT) and by Pitzer models. Literature data on the protonation of carbonate in NaClaq (0.1≤I/mol kg−1 ≤6) were also critically analysed. Both protonation constants of carbonate follow the trend Et4NI>Me4NCl > NaCl. An ion pair formation model designed to take into account the different protonation behaviours of carbonate in different supporting electr…

Aqueous solutionProtonation of carbonateSpecific ion interaction theory (SIT)Ion pair formation modelChemistryInorganic chemistryTetraalkylammonium saltProtonationDependence on ionic strengthElectrolyteIon pairsAnalytical Chemistrychemistry.chemical_compoundIonic strengthTetramethylammonium chlorideAqueous solutionPitzer equationsCarbonateSettore CHIM/01 - Chimica AnaliticaProtonation of carbonate; Dependence on ionic strength; Aqueous solution; Tetraalkylammonium salts; Ion pair formation model; Specific ion interaction theory (SIT); Pitzer equationPitzer equation
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Bile acid–cysteamine conjugates: Structural properties, gelation, and toxicity evaluation

2011

Abstract Design, synthesis, and characterization of six novel bile acid–cysteamine conjugates together with investigation of their structural studies, gelation properties, and preliminary toxicity evaluation, are reported. Solid state properties of selected compounds were studied by means of X-ray diffraction and 13C CPMAS NMR spectroscopy. N-(2-thioethyl)-3α,7α,12α-trihydroxy-5β-cholan-24-amide was shown to exhibit (pseudo)polymorphism, and a single crystal structure of its non-stoichiometric hydrate is reported herein. Cholyl and dehydrocholyl derivatives bearing three functionalities in their steroidal backbone were shown to undergo self-assembly leading to gelation in certain organic so…

BALB 3T3 CellsMagnetic Resonance Spectroscopymedicine.drug_classCysteamineClinical BiochemistryCholic AcidBiochemistryBile Acids and SaltsInhibitory Concentration 50Micechemistry.chemical_compoundEndocrinologyX-Ray DiffractionmedicineAnimalsOrganic chemistryta116Molecular BiologyPharmacologyBile acidUrsodeoxycholic AcidOrganic ChemistryHydrogen BondingNuclear magnetic resonance spectroscopyFibroblastsAmidesCombinatorial chemistrychemistrySolid-state nuclear magnetic resonancePolymorphism (materials science)SolventsLithocholic AcidCysteamineHydrateSingle crystalDeoxycholic AcidConjugateSteroids
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New stratigraphical data on the Middle-Late Jurassic biosiliceous sediments from the Sicanian basin, Western Sicily (Italy)

2008

The reported data present the stratigraphy of several sections across a Middle–Late Jurassic Radiolaritic Unit, well exposed in different thrust sheets pertaining to the Maghrebian chain of Southwestern Sicily. The aim was to define the chronostratigraphical distribution of the Jurassic biosiliceous sedi- mentation in the Sicanian palaeogeographical zone, a deep water basin belonging to the Southern Tethys continental margin. The radiolarian biostratigraphy indicates that the switching from carbonate to siliceous sedimentation in the Sicanian Basin is referable to the Bajocian, as shown by the section of Campofiorito, near Corleone. The biostratigraphical dataset allows the correlation betw…

BasaltMiddle-Late JurassicbasaltsGeologychertsBiostratigraphyStructural basinDeep waterradiolariansPaleontologyMiddle–Late JurassicContinental marginStratigraphyradiolarians; biostratigraphy; cherts; basalts; Middle–Late Jurassic; SicilybiostratigraphySiliceous sediments Mesozoic Sicily Jurassic radiolariaSicilyGeology
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Transition from mildly-tholeiitic to calc-alkaline suite: the case of Chichontepec volcanic centre, El Salvador, Central America

1998

Abstract The Chichontepec volcano is a Plio-Pleistocene composite volcano that erupted lavas ranging from high-alumina basalts to dacites. It experienced a caldera-forming paroxysmal eruption during the early Pleistocene. Pre-caldera lavas are mildly tholeiitic and they evolved mainly by low pressure crystal fractionation, notwithstanding the fact that most mafic lavas (low-MgO high-alumina basalts) retain traces of polybaric evolution. Conversely, post-caldera lavas, which are mainly pyroxene andesites, are clearly calc-alkaline, having evolved by open-system crystal fractionation. Sr–Nd isotopic data and trace elements characteristics indicate that the same mantle source was involved in t…

Basaltgeographygeography.geographical_feature_categoryFractional crystallization (geology)radiogenic isotopesandesitesAndesiteGeochemistryengineering.materialVolcanic rockGeophysicsal-spinelGeochemistry and PetrologyengineeringPlagioclaseal-spinel; andesites; central america; el salvador; high-alumina basalts; radiogenic isotopesIgneous differentiationMaficel salvadorhigh-alumina basaltscentral americaGeologyPetrogenesis
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