Search results for " Io"

showing 10 items of 2766 documents

The Influence of Urban Agglomeration on the Accumulation of Certain Heavy Metal Ions in Tansy (Tanacetum vulgare L.)

2020

Different compounds including toxic heavy metals ions have been used in various industrial branches for ages. Therefore, these compounds are nowadays often identified in the natural environment. Plants usually function like indirect transporters through which heavy metals, in the form of ions, infiltrate from the environment into the human and animals’ food chains. The present paper studied the influence of urban agglomeration on the accumulation of certain heavy metals in tansy. The content of heavy metals ions (Cr, Ni, Cd and Pb) was marked in the tansy leaves. Depending on the location of sampling, large variations in the heavy metal content were observed in the plant material. The resea…

lcsh:GE1-350Tanacetum vulgare L.Urban agglomerationChemistryMetal ions in aqueous solutionanthropogenic areasHeavy metalsnon-anthropogenic areaslcsh:TD1-1066Environmental chemistrylcsh:Environmental technology. Sanitary engineeringheavy metalsenvironmenttanacetum vulgare llcsh:Environmental sciencesEcology Evolution Behavior and SystematicsGeneral Environmental ScienceJournal of Ecological Engineering
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Resonance in Interacting Induced-Dipole Polarizing Force Fields: Application to Force-Field Derivatives

2009

The Silberstein model of the molecular polarizability of diatomic molecules, generalized by Applequist et al. for polyatomic molecules, is analyzed. The atoms are regarded as isotropically polarizable points located at their nuclei, interacting via the fields of their induced dipoles. The use of additive values for atom polarizabilities gives poor results, in some cases leading to artificial predictions of absorption bands. The molecular polarizability of methane and its derivative are computed. The agreement with experimental mean molecular polarizabilities is within 1–5%. A hypothesis is indispensable for a suitable representation of polarizability derivative.

lcsh:T55.4-60.8Molecular physicsForce field (chemistry)lcsh:QA75.5-76.95Theoretical Computer Scienceelectric field gradientPolarizabilityAtomPhysics::Atomic and Molecular ClustersMoleculederivativelcsh:Industrial engineering. Management engineeringPhysics::Atomic PhysicsPhysics::Chemical PhysicsPhysicspolarizing force fieldNumerical AnalysisPolyatomic iondipole momentDiatomic moleculepolarizabilityelectric fieldComputational MathematicsDipoleComputational Theory and Mathematicsresonanceinteracting induced-dipole polarizationlcsh:Electronic computers. Computer scienceElectric field gradientAlgorithms
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Modification of the Structure and Nano-Mechanical Properties of LiF Crystals Under Irradiation with Swift Heavy Ions

2011

The modifications of the structure and hardness of LiF crystals under high-fluence irradiation with MeV- and GeV-energy Au ions have been studied using nanoindentation and atomic force microscopy. The formation of ion-induced dislocations and bulk nanostructures consisting of grains with nanoscale dimensions (50 nm - 100 nm) has been observed. The structural modifications are accompanied by a strong ion-induced hardening which is related to dislocation impeding by assemblies of defect aggregates, dislocation loops of vacancy and interstitial types and grain boundaries. For MeV ions, the modifications are localized in a thin surface layer (few mm) where much higher density of deposited energ…

lcsh:TN1-997LiF crystalsNanostructureMaterials sciencenanoindentationhardeningMeV-energy ionsNanoindentationMolecular physicsnanostructuringIonCondensed Matter::Materials ScienceCrystallographyVacancy defectHardening (metallurgy)General Materials ScienceGrain boundaryIrradiationDislocationlcsh:Mining engineering. MetallurgyMaterials Science
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Wo3 and ionic liquids: A synergic pair for pollutant gas sensing and desulfurization

2020

This review deals with the notable results obtained by the synergy between ionic liquids (ILs) and WO3 in the field of pollutant gas sensing and sulfur removal pretreatment of fuels. Starting from the known characteristics of tungsten trioxide as catalytic material, many authors have proposed the use of ionic liquids in order to both direct WO3 production towards controllable nanostructures (nanorods, nanospheres, etc.) and to modify the metal oxide structure (incorporating ILs) in order to increase the gas adsorption ability and, thus, the catalytic efficiency. Moreover, ionic liquids are able to highly disperse WO3 in composites, thus enhancing the contact surface and the catalytic abilit…

lcsh:TN1-997Pollutant gasesMaterials scienceOxidechemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compoundAdsorptionWO<sub>3</sub>WO3General Materials ScienceDesulfurizationlcsh:Mining engineering. Metallurgyionic liquidDesulfurization; Gas sensor; Ionic liquids; Pollutant gases; WO; 3pollutant gaseMetals and AlloysSettore CHIM/06 - Chimica Organica021001 nanoscience & nanotechnologySulfurTungsten trioxide0104 chemical sciencesFlue-gas desulfurizationIonic liquidschemistryChemical engineeringIonic liquid0210 nano-technologyGas sensorHydrodesulfurization
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Liquid Phase Micro-Extraction of Linear Alkylbenzene Sulfonate Anionic Surfactants in Aqueous Samples

2011

Hollow fiber liquid phase micro-extraction (LPME) of linear alkylbenzene sulfonates (LAS) from aqueous samples was studied. Ion pair extraction of C10, C11, C12 and C13 homologues was facilitated with trihexylamine as ion-pairing agent, using di-n-hexylether as solvent for the supported liquid membrane (SLM). Effects of extraction time, acceptor buffer concentration, stirring speed, sample volume, NaCl and humic acids were studied. At 10–50 µg L−1 linear R2-coefficients were 0.99 for C10 and C11 and 0.96 for C12. RSD was typically ~15%. Three observations were especially made. Firstly, LPME for these analytes was unusually slow with maximum enrichment observed after 15–24 h (depending on sa…

linear alkylbenzene sulfonateLinear alkylbenzenesurfactantFiltration and Separationlcsh:Chemical technologyArticleion-pairingchemistry.chemical_compoundPulmonary surfactantMass transferChemical Engineering (miscellaneous)lcsh:TP1-1185lcsh:Chemical engineeringchemistry.chemical_classificationAqueous solutionChromatographyChemistryProcess Chemistry and TechnologyExtraction (chemistry)lcsh:TP155-156SolventMembranelinear alkylbenzene sulfonate; extraction; liquid-phase microextraction; ion-pairing; method development; environmental analysis; surfactantenvironmental analysisextractionliquid-phase microextractionmethod developmentCounterionMembranes
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The electric properties of ionic solutions: a molecular dynamics (preliminary) study

2011

lipid bilayer ionic solutions molecular dynamics non equilibriumlipid bilayer ionic solution molecula drynamics electric fieldSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)
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Protonazione del p-nitrofenato di sodio in liquidi ionici: una "sonda" per la determinazione della forza acida

liquidi ionici acidità coppie ionicheSettore CHIM/06 - Chimica Organica
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LIQUIDI IONICI E CARBON DOTS UNITI NEI GEL IBRIDI!

2020

La ricerca di materiali sempre più efficienti abbraccia svariati campi della società attuale e l’unione di due componenti con peculiarità complementari può generare materiali altamente innovativi. I gel formati da carbon nanodots e liquidi ionici non soltanto preservano le caratteristiche dei singoli componenti, ma ne migliorano le prestazioni, generando così un materiale ibrido performante e facilmente modulabile in base alle applicazioni richieste.

liquidi ionici carbon dots gel supramolecolari
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Complessi liquido ionico-cobalto: un’interazione termocromica

2019

Le ben note proprietà chimico-fisiche dei liquidi ionici (ILs), unite alla versatilità strutturale, sono alla base delle loro numerose e differenti applicazioni. In questo lavoro, si presenta un’interazione termocromica reversibile, sia in soluzione che in un film polimerico, tra un IL portante sul catione un residuo gluconammidico e il sale di cobalto Co(NTf2)2. I gruppi ossidrilici sul catione e l’anione bromuro dell’IL coordinano il Co al variare della temperatura applicata. A temperatura ambiente il complesso OH-Co risulta ottaedrico (rosa) mentre, intorno ai 60 °C, la geometria diviene tetraedrica con lo ione bromuro che coordina il Co (blu). Lo studio VT UV-vis (Figura 1) ha permesso …

liquidi ionici termocromismoSettore CHIM/06 - Chimica Organica
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Room-Temperature Magnetic Bistability in a Salt of Organic Radical Ions

2021

International audience; Cocrystallization of 7,7′,8,8′-tetracyanoquinodimethane radical anion (TCNQ −•) and 3-methylpyridinium-1,2,3,5dithiadiazolyl radical cation (3-MepyDTDA +•) afforded isostructural acetonitrile (MeCN) or propionitrile (EtCN) solvates containing cofacial π dimers of homologous components. Loss of lattice solvent from the diamagnetic solvates above 366 K affords a high-temperature paramagnetic phase containing discrete TCNQ −• and weakly bound π dimers of 3-MepyDTDA +• , as evidenced by X-ray diffraction methods and magnetic susceptibility measurements. Below 268 K, a first-order phase transition occurs, leading to a low-temperature diamagnetic phase with TCNQ −• σ dimer…

magneettiset ominaisuudetDimer02 engineering and technologyGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistry010402 general chemistry021001 nanoscience & nanotechnologyvapaat radikaalit01 natural sciencesBiochemistryTetracyanoquinodimethaneMagnetic susceptibilityCatalysis0104 chemical scienceschemistry.chemical_compoundParamagnetismCrystallographyColloid and Surface ChemistryRadical ionchemistryDiamagnetismPropionitrileIsostructural0210 nano-technologyorgaaniset yhdisteet
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