Search results for " solution"

showing 10 items of 3084 documents

Cysteamine and its homoleptic complexes with group 12 metal ions. Differences in the coordination chemistry of ZnII, CdII, and HgII with a small N,S-…

2005

2-Ammoniumethanethiolate, (-)SCH(2)CH(2)NH(3)(+), the first structurally characterized zwitterionic ammoniumthiolate, is the stable form of cysteamine (HL) in the solid state and in aqueous solution. Reactions of ZnCl(2), Cd(Oac)(2), and HgCl(2) with cysteamine and NaOH in a 1:2:2 ratio, respectively, lead to the homoleptic complexes ML(2). Their single-crystal X-ray structures demonstrate basic differences in the coordination chemistry of Zn(II), Cd(II), and Hg(II). While chelating N,S-coordination modes are found for all metal ions, Zn(II) forms a mononuclear complex with a distorted tetrahedral Zn(N(2)S(2)) coordination mode, whereas Hg(II) displays a dimer with Hg(N(2)S(2)) coordinated …

chemistry.chemical_classificationAqueous solutionLigandStereochemistryMetal ions in aqueous solutionSolid-stateCoordination complexInorganic Chemistrychemistry.chemical_compoundchemistryGroup (periodic table)Polymer chemistryCysteaminePhysical and Theoretical ChemistryHomolepticInorganic chemistry
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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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A Facile Approach for Transferring Hydrophobic Magnetic Nanoparticles into Water-Soluble Particles

2008

A novel, easy and high-efficient method is described for transferring hydrophobic magnetic Fe 3 O 4 nanoparticles from organic to aqueous solution by wrapping a thermo-responsive and photocrosslinkable poly(N-isopropylacrylamide) (PNIPAm) terpolymer around the particles. The wrapping procedure is introduced by the co-nonsolvent transition of PNIPAm in the mixing solvent and the polymer can dissolve in water carrying Fe 3 O 4 nanoparticles by noncovalent interaction. The temperature-dependant and magnetic properties of the water-soluble particles are characterized in this paper.

chemistry.chemical_classificationAqueous solutionMaterials scienceHydrodynamic radiusPolymers and PlasticsOrganic ChemistryNanoparticlePolymerCondensed Matter PhysicsSolventchemistryPolymer chemistryMaterials ChemistryCopolymerMagnetic nanoparticlesThermal stabilityPhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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Langmuir-Blodgett films of biocompatible poly(HPMA)-block-poly(lauryl methacrylate) and poly(HPMA)-random-poly(lauryl methacrylate): influence of pol…

2010

Membranes based on functional biocompatible polymers can be regarded as a useful model system to study biological interactions, e.g. antibody-antigen interactions or protein polymer interactions. These model systems may give a better insight into these processes and may help to find suitable polymeric structures offering biocompatibility as well as reduced polymer protein interaction. In this respect, Langmuir-Blodgett (LB) layer formation at the air/water (A/W) interface is studied in respect to polymer architecture in this article. For this purpose, narrowly distributed N-(2-hydroxypropyl)-methacrylamide (HPMA) random and block copolymers have been prepared by the RAFT polymerization meth…

chemistry.chemical_classificationAqueous solutionMaterials scienceMagnetic Resonance SpectroscopyBiocompatibilityPolymersPolymer architectureBiocompatible MaterialsMembranes ArtificialSurfaces and InterfacesPolymerCondensed Matter PhysicsMicroscopy Atomic ForceLangmuir–Blodgett filmMembranechemistryPolymer chemistryElectrochemistryCopolymerMethacrylatesGeneral Materials ScienceReversible addition−fragmentation chain-transfer polymerizationSpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Structure of e-beam sculptured poly(N-vinylpyrrolidone) networks across different length-scales, from macro to nano

2013

Abstract Study of macromolecular structure and dynamics of networks formed by pulsed electron-beam irradiation of poly(N-vinyl pyrrolidone) (PVP) aqueous solutions, at relatively low energy per pulse and across different concentration regimes, provides the basis for the understanding of a new generation of functional nanostructures. Networks are the result of the follow–up reactions initiated by a continuous series of electron pulse-generated hydroxyl radicals, which may have a different fate at the variance of polymer concentration. Different spectroscopic techniques, FT-IR, 13 C { 1 H} CP-MAS NMR and Raman, applied to characterize the formed networks, describe a profound modification of t…

chemistry.chemical_classificationAqueous solutionMaterials scienceNanostructurePolymers and PlasticsOrganic ChemistryNanotechnologyPolymersymbols.namesakeChemical engineeringchemistryNano-Materials ChemistrysymbolsElectron beam processingStatic light scatteringSettore CHIM/07 - Fondamenti Chimici Delle TecnologieRaman spectroscopyNanogels Irradiation Poly(N-vinylpyrrolidone)NanogelPolymer
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Helix–Coil Transition in Cylindrical Brush Polymers with Poly-l-lysine Side Chains

2012

Cylindrical brush polymers with poly-l-lysine side chains were prepared by grafting lysine NCA from a macroinitiator via living ring-opening polymerization. The main chain degree of polymerization of the methacrylate main chain was Pw = 870, the side chains consisted of 25 and 55 lysine repeat units, respectively. Upon deprotection, the cylindrical brush polymers in 0.005 M NaBr exhibited an almost rodlike conformation with a Kuhn statistical segment length of several hundred nanometers. Cryo-TEM as well as AFM in aqueous solution clearly demonstrated pronounced undulations along the main chain at low ionic strength which could not be detected at higher salt concentrations. With increasing …

chemistry.chemical_classificationAqueous solutionMaterials sciencePolymers and PlasticsOrganic ChemistryPolymerDegree of polymerizationMethacrylateInorganic ChemistryFolding (chemistry)CrystallographyPolymerizationchemistryHelixMaterials ChemistrySide chainMacromolecules
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Synthesis of gold nanotubes with variable wall thicknesses

2013

We report the synthesis of gold nanotubes with variable wall thicknesses that is accomplished by the deposition of sacrificial hydrophobic polymer cores followed by gold shells within an anodic aluminum oxide template. We demonstrate that by varying polymer core hydrophobicity, the resulting gold shell thickness can be varied. There are two requirements for gold shell formation: (1) the polymer core must be able to be electrodeposited into a tubular (as opposed to wire-like) structure, and (2) the polymer must be hydrophobic, such that it collapses upon exposure to an aqueous solution. An array of gold nanotubes has variable plasmonic properties and can function as a surface enhanced Raman …

chemistry.chemical_classificationAqueous solutionMaterials scienceRenewable Energy Sustainability and the EnvironmentShell (structure)Core (manufacturing)General ChemistrySubstrate (electronics)PolymerSurface-enhanced Raman spectroscopychemistryGeneral Materials ScienceComposite materialPlasmonDeposition (law)J. Mater. Chem. A
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Hybrid processes coupling photocatalysis and membranes for degradation of organic pollutants in water

2002

Abstract Tests of degradation in a photocatalytic membrane system with the lamp immersed in the suspension inside the photoreactor have been carried out by using polycrystalline TiO2 (Degussa P25) as catalyst and humic acids, organic dyes, 4-nitrophenol as pollutants. The influence of the type of nanofiltration membrane, initial concentration of pollutant and pH on the photodegradation rate was investigated in discontinuous and continuous configurations. Two membranes were tested, i.e. NF-PES-010 (Celgard, Germany) of polyethersulphone and NTR-7410 (Nitto-Denko, Japan) of sulphonated polyethersulphone. The last one was chosen for all of the photoreactivity experiments because permeability a…

chemistry.chemical_classificationAqueous solutionMembraneMembrane reactorChemistryInorganic chemistryPhotocatalysisHumic acidPortable water purificationGeneral ChemistryNanofiltrationPhotodegradationCatalysisCatalysis Today
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Palladium(II) sequestration by phytate in aqueous solution. Speciation analysis and ionic medium effects.

2010

Environmental context.In the last 20 years, the demand for palladium and other platinum-group elements has intensified, causing a significant increase in their concentration in the environment, with particular accumulation in urban areas. Knowledge about Pd2+ speciation in aqueous media is fundamental for the understanding of its biological and environmental activity in contaminated areas. Phytic acid appears to be a good sequestering agent towards Pd2+ under various conditions, indicating its potential use in the remediation of contaminated sites. Abstract. Palladium(II) speciation in the presence of phytate (Phy12–) was studied by H+ ion selective electrode (ISE) potentiometry at 25°C in…

chemistry.chemical_classificationAqueous solutionMetal ions in aqueous solutionInorganic chemistryFluorescence spectrometrychemistry.chemical_elementcomplexes stability constantsPhytateIon selective electrodeDivalentMetalchemistryComplexesGeochemistry and PetrologyChemistry (miscellaneous)Ionic strengthvisual_artvisual_art.visual_art_mediumEnvironmental ChemistrySettore CHIM/01 - Chimica AnaliticaStability constantsComplexes; Stability constants; Phytate; PalladiumPalladiumPalladium
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Expanding the NUIG MOF family: synthesis and characterization of new MOFs for selective CO2 adsorption, metal ion removal from aqueous systems, and d…

2021

Metal organic frameworks (MOFs) have attracted considerable attention in recent years due to their use in a wide range of environmental, industrial and biomedical applications. The employment of benzophenone-4,4'-dicarboxylic acid (bphdcH2) in MOF chemistry provided access to the 3D mixed metal MOFs [CoNa2(bphdc)2(DMF)2]n (NUIG2) and [ZnK2(bphdc)2(DMF)2]n (NUIG3), and the 2D homometallic MOF [Co2(OH)(bphdcH)2(DMF)2(H2O)2]n(OH)·DMF (1·DMF). 1·DMF is based on a dinuclear SBU and consists of interpenetrating networks with an sql topology. Dc magnetic susceptibility studies were carried out in 1·DMF and revealed the presence of weak antiferomagnetic exchange interactions between the metal centr…

chemistry.chemical_classificationAqueous solutionMetal ions in aqueous solutionMagnetic susceptibilityInorganic ChemistryMetalAdsorptionDicarboxylic acidchemistryvisual_artPolymer chemistryvisual_art.visual_art_mediumMoleculeMetal-organic frameworkDalton Transactions
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