Search results for "Bonding"

showing 10 items of 996 documents

Solution properties of polyelectrolytes

1993

Abstract Aqueous size-exclusion chromatography was used to analyse the elution behaviour of several standard ionic polymers, including poly( l -glutamic acid), sodium poly(styrene sulphonate) and poly(acrylic acid), different in nature and chain flexibility, as a function of the pH and ionic strength of the eluent. Two organic-based hydrophilic packings, Spherogel TSK PW4000 and Ultrahydrogel 250, were tested in order to select the optimal conditions of macromolecular separation, and the results obtained for each column were compared. A set of calibration graphs for the above polyions as a function of eluent pH and ionic strength were obtained and compared with those obtained for uncharged …

chemistry.chemical_classificationAqueous solutionChromatographyChemistryElutionOrganic ChemistrySize-exclusion chromatographyIonic bondingPolymerGeneral MedicineElectrostaticsBiochemistryPolyelectrolyteAnalytical ChemistryGel permeation chromatographychemistry.chemical_compoundColumn chromatographyIonic strengthSurface chargeAcrylic acidJournal of Chromatography A
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Characterization of transparent silver loaded poly(l-lactide) films produced by melt-compounding for the sustained release of antimicrobial silver io…

2014

Abstract In the present study, thermally stable silver complexes were produced and incorporated into a poly-( l -lactide) (PLA) matrix by melt-compounding. The effect of the different formulations on the mechanical and color properties was first evaluated. Additionally, the release of silver ions to an aqueous environment was also monitored over time by anodic stripping voltammetry and correlated with the antimicrobial performance against Salmonella enterica. The incorporation of some silver compounds with contents of 1 wt% did not affect the mechanical or optical properties of the films. The films showed a good potential for application in surface treatment and demonstrated a sustainable, …

chemistry.chemical_classificationAqueous solutionLactideMaterials scienceIonic bondingPolymerSilver nanoparticleFood packagingchemistry.chemical_compoundAnodic stripping voltammetrychemistryChemical engineeringCompoundingOrganic chemistryFood ScienceBiotechnologyFood Control
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Salt partitioning in ionized, thermo-responsive hydrogels: perspective to water desalination

2021

Charged hydrogels are capable of swelling in aqueous salt solutions, whereby part of the salt ions is repelled due to the presence of fixed charged groups inside the hydrogel. This effect creates a concentration gradient between the absorbed solution and the surrounding fluid known as salt partitioning, offering a potential for these materials to be employed to desalinate saltwater. If the charged hydrogels are thermo-sensitive as well, then the purer, absorbed solution can be recovered by shrinking the hydrogels upon temperature change. To tailor that potential in water-purification and desalination applications, the main parameters influencing the salt partitioning, the deswelling of the …

chemistry.chemical_classificationAqueous solutionMaterials science010304 chemical physicsGeneral Physics and AstronomySalt (chemistry)Ionic bondingCharge density010402 general chemistry01 natural sciencesDesalination0104 chemical scienceschemistry.chemical_compoundchemistryChemical engineering0103 physical sciencesSelf-healing hydrogelsmedicinePhysical and Theoretical ChemistrySwellingmedicine.symptomAcrylic acidThe Journal of Chemical Physics
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Speciation of tin(II) in aqueous solution: thermodynamic and spectroscopic study of simple and mixed hydroxocarboxylate complexes

2013

This contribution reports the results of potentiometric and Mossbauer investigations on the formation, stability, and structure of binary and ternary mono- and binuclear complexes of Sn2+ with three hydroxocarboxylic ligands (namely L = tartrate, malate, and citrate) and chloride at T = 298.15 K in different ionic media and ionic strengths (0.15 and 1.00 mol dm−3 in NaCl(aq) and 1.00 mol dm−3 in NaNO3(aq)). The stability constants of various simple Sn i H j L (2+−) and mixed Sn i H j L k Cl (2+−−) species obtained in the different experimental conditions are reported, and various speciation diagrams of the simple and mixed systems are shown in different conditions. The sequestering ability …

chemistry.chemical_classificationAqueous solutionMössbauer spectroscopyPotentiometric titrationEnthalpyInorganic chemistrySequestrationIonic bondingComputer programGeneral ChemistryChlorideCoordination chemistryCoordination complexTrigonal bipyramidal molecular geometrychemistrySettore CHIM/03 - Chimica Generale E InorganicamedicineMetal complexeSettore CHIM/01 - Chimica AnaliticaStability constantsTernary operationmedicine.drugMonatshefte für Chemie - Chemical Monthly
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Ionic transport characteristics of negatively and positively charged conical nanopores in 1:1, 2:1, 3:1, 2:2, 1:2, and 1:3 electrolytes

2019

We study experimentally the current (I)-voltage (V) curves of 1:1, 2:1, 3:1, 2:2, 1:2, and 1:3 electrolytes in positively and negatively charged conically-shaped pores of nanoscale dimensions. The positive charges are poly(allylamine hydrochloride) chains functionalized on the pore surface by electrostatic interactions while the negative charges are carboxylic acid groups. Under physiological conditions, these fixed-charge groups are ionized and strongly interact with the different monovalent, divalent, and trivalent ions in the pore solution. The current rectification of the I-V curves and the membrane potentials provide fundamental information on the interaction of the pore charge groups …

chemistry.chemical_classificationCarboxylic acidIonic bonding02 engineering and technologyElectrolyte010402 general chemistry021001 nanoscience & nanotechnologyElectrostatics01 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsDivalentIonBiomaterialsNanoporeColloid and Surface ChemistrychemistryChemical physics0210 nano-technologyTransport phenomenaJournal of Colloid and Interface Science
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Crystal structure of the chalcone (E)-3-(furan-2-yl)-1-phenylprop-2-en-1-one

2015

The crystal packing of the compound is described by an inter­molecular arrangement with the mol­ecules as inter­laced layers in a zigzag fashion, denoting inter­acting self-complementary dimers mainly by the localization of weak hydrogen bonds in a head-to-tail arrangement.

chemistry.chemical_classificationChalconecrystal structureCrystallographyDouble bondHydrogen bondChemistryStereochemistryClaisen–Schmidt reactionbiological activityGeneral ChemistryCrystal structureCondensed Matter PhysicsRing (chemistry)hydrogen bondingAcceptorResearch CommunicationsCrystalchemistry.chemical_compoundCrystallographychalcone derivativezigzag fashion.QD901-999FuranGeneral Materials ScienceActa Crystallographica Section E: Crystallographic Communications
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Chemical speciation of organic matter in natural waters. Interaction of nucleotide 5′ mono-, di- and triphosphates with major components of seawater

2004

AbstractThe interactions of nucleotide 5’ mono-, di- and triphosphates in a multicomponent ionic medium simulating the macro-composition of seawater (Na+, K+, Ca2+, Mg2+, Cl-, SO42-, Synthetic Sea Water, SSW) have been investigated at different ionic strengths and at T= 25°C. A chemical speciation model, according to which all the internal interactions between the components of the ionic medium are taken into account, was applied to determine the effective formation constants of species in the nucleotide-seawater system. The results were compared to protonation parameters calculated from single electrolyte systems. A simpler model (SSW considered as a single salt BA, with Bz+ and Az-), repr…

chemistry.chemical_classificationChemical Health and SafetyHealth Toxicology and MutagenesisInorganic chemistrySalt (chemistry)Ionic bondingProtonationElectrolytenucleotideToxicologyorganic natural matterIonspeciationchemistryStability constants of complexesspeciation; nucleotide; seawater; organic natural matterQualitative inorganic analysisSeawaterChemical speciation of organic matter. Complex formation. Natural waters. Nucleotidesseawater
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POSS nanostructures in catalysis

2020

Polyhedral oligomeric silsesquioxanes (POSS) are organic-inorganic hybrid molecules piquing the interest of researchers thanks to their synergistic features. The great versatility of POSS nanostructures arises from the easy tunability of peripheral organic moieties combined with the high thermal and chemical stability of the inner inorganic core. In this review, we highlight the use of POSS nanostructures as molecular precursors for the synthesis of homogeneous and heterogeneous catalysts able to promote many processes including alkene epoxidation, C-C bond formation, CO2 conversion, "click reactions", hydrogenation, and ethylene polymerisation, among others. In this scenario, POSS units fo…

chemistry.chemical_classificationChemical substanceMaterials scienceNanostructureMolecular modelIonic bondingNanotechnologySettore CHIM/06 - Chimica OrganicaPolymerhomogeneous catalysiCatalysisCatalysischemistryheterogeneous catalysiorganometallic catalysisMoleculeChemical stabilityPolyhedral oligomeric silsesquioxaneCatalysis Science & Technology
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Characterization of gas phase aggregates of bis(2-ethylhexyl)sulfosuccinate (AOT) and divalent metal ions. Elimination of radical species in the deco…

2012

Structure and properties of even-electron anionic species formed by bis(2-ethylhexyl)sulfosuccinate (AOT) and divalent metal ions (MII) with stoichiometry [AOTMIICl2]– have been investigated by using electrospray ionization and different mass spectrometry techniques, such as high resolution, accurate mass measurements, collision-induced dissociation (CID) multiple-stage mass spectrometry. Owing to CID, eliminations of neutrals, mainly consisting in hydrochloric acid, 2-ethyl-1-hexene and 2-ethylhexanol, and an unexpected loss of an alkyl radical have been observed. The radical anions [C4HO6SMIICl]–• so produced have been characterized by MS3 experiments. Density functional theory calculatio…

chemistry.chemical_classificationChemistryElectrospray ionizationsurfactantInorganic chemistryIonic bondingHydrochloric acidMass spectrometryTandem mass spectrometryeven electron ruleDissociation (chemistry)chemistry.chemical_compoundsurfactants; electrospray; even electron rule; tandem mass spectrometry; theoretical calculationstandem mass spectrometryelectrospraySpectroscopyStoichiometryAlkyltheoretical calculationsSettore CHIM/02 - Chimica Fisica
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Group 14 Metalloles, Ionic Species and Coordination Compounds

2009

1 Introduction 2 Synthesis 3 Organic Chemical Properties of Group 14 Metalloles 4 Polymeric Silole-Containing π-Conjugated Systems 5 Ionic Species and Coordination Compounds 6 Addendum 7 Conclusion 8 Acknowledgements Keywords: five-membered heterocyclic dienes; heterocyclopentadienes - heteroles or metalloles; group 14 metalloles, ionic species and coordination compounds; gas-phase pyrolysis of silacyclopent-3-enes; organometallic dihalide reaction with dilithio reagent; group 14 metalloles; HOMO stabilization; polymeric silole-containing pi-conjugated systems

chemistry.chemical_classificationChemistryGroup (periodic table)ReagentOrganic chemistryIonic bondingPyrolysisCoordination complex
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