Search results for "Metal ions in aqueous solution"

showing 10 items of 256 documents

Kinetic and equilibrium study for cadmium and copper removal from aqueous solutions by sorption onto mixed alginate/pectin gel beads

2013

Abstract Kinetic and equilibrium studies have been carried out to evaluate Cd(II) and Cu(II) sorption from aqueous solution by calcium alginate and new synthesized hybrid calcium alginate/pectate gel beads with different alginate/pectate concentration ratios. Physical and chemical properties of the beads were characterized by different techniques (SEM, EDX, TGA). The best experimental pH conditions were selected on the basis of a study on the acid–base properties of pectin and alginate in aqueous solution and their ability to act as sequestering agents for copper(II) and cadmium(II) ions. Calcium released during the sorption process was determined in order to elucidate a possible ion exchan…

LangmuirAqueous solutionCalcium alginateAlginate Pectin Gel beads Adsorption Metal removalIon exchangeChemistryProcess Chemistry and TechnologyMetal ions in aqueous solutionInorganic chemistrySorptioncomplex mixturesPollutionchemistry.chemical_compoundAdsorptionChemical Engineering (miscellaneous)Freundlich equationSettore CHIM/01 - Chimica AnaliticaWaste Management and Disposal
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Scanning electrochemical microscopy as a probe of Ag+ binding kinetics at Langmuir phospholipid monolayers

2005

A new method has been developed for measuring local adsorption rates of metal ions at interfaces based on scanning electrochemical microscopy (SECM). The technique is illustrated with the example of Ag+ binding at Langmuir phospholipid monolayers formed at the water/air interface. Specifically, an inverted 25 microm diameter silver disc ultramicroelectrode (UME) was positioned in the subphase of a Langmuir trough, close to a dipalmitoyl phosphatidic acid (DPPA) monolayer, and used to generate Ag+ via Ag electro-oxidation. The method involved measuring the transient current-time response at the UME when the electrode was switched to a potential to electrogenerate Ag+. Since the Ag+/Ag couple…

LangmuirBinding SitesSilverTime FactorsSurface PropertiesChemistryMetal ions in aqueous solutionAnalytical chemistryPhosphatidic AcidsGeneral Physics and AstronomyUltramicroelectrodeMicroscopy Scanning ProbeSurface pressureKineticsScanning electrochemical microscopyAdsorptionCationsElectrodeMonolayerElectrochemistrylipids (amino acids peptides and proteins)AdsorptionPhysical and Theoretical ChemistryPhospholipidsPhysical Chemistry Chemical Physics
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Sorption and mechanism studies of Cu2+, Sr2+ and Pb2+ ions on mesoporous aluminosilicates/zeolite composite sorbents

2020

Abstract The research aimed to develop a novel mesoporous aluminosilicate/zeolite composite by the template co-precipitation method. The effect of aluminosilicate (AlSi) and zeolite (NaY) on the basic properties and adsorption capacity of the resultant composite was conducted at different mass ratios of AlSi/NaY (i.e., 5/90, 10/80, 15/85, 20/80, and 50/50). The adsorption characteristics of such composite and its feedstock materials (i.e., aluminosilicates and zeolite) towards radioactive Sr2+ ions and toxic metals (Cu2+ and Pb2+ ions) in aqueous solutions were investigated. Results indicated that BET surface area (SBET), total pore volume (VTotal), and mesopore volume (VMeso) of prepared m…

LangmuirEnvironmental EngineeringAqueous solutionIon exchangeChemistryMetal ions in aqueous solution02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAdsorptionAluminosilicate0210 nano-technologyZeoliteWater Science and TechnologyNuclear chemistryBET theoryWater Science and Technology
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Synthesis of zeolite/geopolymer composite for enhanced sequestration of phosphate (PO43−) and ammonium (NH4+) ions; equilibrium properties and realis…

2021

Abstract Zeolite impeded geopolymer (Z/G) was synthesized from natural kaolinite and diatomite. The structure (Z/G) was characterized as an enhanced adsorbent for PO43− and NH4+ ions from aqueous solutions, groundwater, and sewage water. The synthetic Z/G structure exhibits sequestration capacities of 206 mg/g and 140 mg/g for PO43− and NH4+, respectively which are higher values than the recognized results for the geopolymer and other adsorbents in literature. The sequestration reactions of PO43− and NH4+ by Z/G are of Pseudo-Second order kinetic behavior considering both the Chi-squared (χ2) and correlation coefficient (R2) values. The sequestration reactions occur in homogenous and monola…

LangmuirEnvironmental EngineeringAqueous solutionIon exchangeChemistryMetal ions in aqueous solutionInorganic chemistryGeneral MedicineManagement Monitoring Policy and LawGeopolymerAdsorptionKaoliniteZeoliteWaste Management and DisposalJournal of Environmental Management
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Metal–Organic Frameworks as Playgrounds for Reticulate Single-Molecule Magnets

2019

Achieving an accurate control on the final structure of Metal-Organic Frameworks (MOFs) is mandatory to obtain target physical properties. Here we describe how the combination of a metalloligand design strategy and a post-synthetic method is a versatile and powerful approach to success on this extremely difficult task. In a first stage, a novel oxamato-based tetranuclear cobalt(III) complex with a tetrahedron-shape geometry is used, for the first time, as metalloligand toward cal-cium(II) cations to lead a diamagnetic Ca(II)-Co(III) three-dimensional (3D) MOF (1). In a second stage, in a single-crystal to single-crystal manner the calcium(II) ions are replaced by terbium (III), dysprosium(I…

Lanthanide010405 organic chemistryMetal ions in aqueous solutionQuímica organometàl·licachemistry.chemical_elementTerbium010402 general chemistry01 natural sciencesMagnetic susceptibility0104 chemical sciencesInorganic ChemistryCrystallographychemistryDysprosiumMoleculeMetal-organic frameworkPhysical and Theoretical ChemistryIsostructuralInorganic Chemistry
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Synthesis, structural characterization and electrochemical and magnetic studies of M(hfac)2 (M = CuII, CoII) and Nd(hfac)3 complexes of 4-amino-TEMPO

2020

Three mononuclear complexes [M(hfac)x(ATEMPO)y], where M = Cu (11) and Co (12), x = y = 2; M = Nd (13), x = 4, y = 1, and two polynuclear complexes [{Cu(hfac)2(ATEMPO)}n], where n = 2 (14) and 4 (15), were obtained by the reaction of M(hfac)x (M = CuII, CoII, NdIII; x = 2, 3) with 4-amino-TEMPO (4-amino-2,2,6,6-tetramethylpiperidin-N-oxyl) in good yields and their structural, electrochemical and magnetic properties were examined. In all cases, the radical is coordinated to the metal through the amino group, except 15, and the metal ions have an octahedral geometry, except 13. Different coordination architectures of the copper complexes were obtained as a function of the stoichiometry and so…

LanthanideChemistryMetal ions in aqueous solutionRadicalSupramolecular chemistrychemistry.chemical_elementNitroxylCopperInorganic ChemistryMetalCrystallographychemistry.chemical_compoundvisual_artOctahedral molecular geometryvisual_art.visual_art_mediumDalton Transactions
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Coordinatively Unsaturated Lanthanide(III) Helicates: Luminescence Sensors for Adenosine Monophosphate in Aqueous Media

2016

Coordinatively unsaturated double-stranded helicates [(H2 L)2 Eu2 (NO3 )2 (H2 O)4 ](NO3 )4 , [(H2 L)2 Tb2 (H2 O)6 ](NO3 )6 , and [(H2 L)2 Tb2 (H2 O)6 ]Cl6 (H2 L=butanedioicacid-1,4-bis[2-(2-pyridinylmethylene)hydrazide]) are easily obtained by self-assembly from the ligand and the corresponding lanthanide(III) salts. The complexes are characterized by X-ray crystallography showing the helical arrangement of the ligands. Co-ligands at the metal ions can be easily substituted by appropriate anions. A specific luminescence response of AMP in presence of ADP, ATP, and other anions is observed. Specificity is assigned to the perfect size match of AMP to bridge the two metal centers and to replac…

LanthanideCoordination sphereadenosine monophosphateStereochemistryMetal ions in aqueous solutionHydrazide010402 general chemistry01 natural sciencesCatalysisMetalchemistry.chemical_compoundluminescencelanthanidesta116sensingQuenching (fluorescence)ChemistryLigand010405 organic chemistryhelicatesGeneral ChemistryGeneral Medicine0104 chemical sciences3. Good healthCrystallographyvisual_artvisual_art.visual_art_mediumLuminescenceAngewandte Chemie International Edition
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Extended dipyrrin ligands : candidates for optical metal ion detection under competitive conditions

2017

Acylhydrazone based extended dipyrrins L1-H and L2-H are introduced as complexometric ppb sensitive metal ion detectors. The binding of lanthanide, transition as well as post-transition metal ions is followed by UV-Vis measurements. The carbohydrate based ligand L2 is water soluble and thus can act as a metal ion sensor in this medium.

LanthanideMetal ions in aqueous solutionInorganic chemistrymetal ion detection010402 general chemistry01 natural sciencesCatalysisMetalMaterials Chemistryta116water solubility010405 organic chemistryLigandChemistryMetals and AlloysGeneral Chemistrydipyrrin ligands0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIon sensorWater solublevisual_artCeramics and Compositesvisual_art.visual_art_mediumzinc complexesChemical Communications
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Syntheses, characterisation, magnetism and photoluminescence of a homodinuclear Ln(III)-Schiff base family.

2009

A novel family of homodinuclear complexes of the general formula [Ln(2)L(2)(X)(2)] (where Ln = Nd(3+), Pr(3+), Sm(3+) and Tb(3+) for 1, 2, 3 and 4, respectively and X, the coordinated NO(3)(-) or Cl(-) anion) has been synthesised from the corresponding lanthanide(III) salts with the pentadentate dianionic Schiff base ligand, H(2)L [N(1),N(3)-bis(salicylideneimino)diethylenetriamine], that exhibits a N(3)O(2) donor set. Single crystal X-ray diffraction studies evidenced the isostructurality of this family of centrosymmetric neutral dinuclear entities where the Ln(III) metal centres are coupled together by two phenolato oxygen atoms belonging to two units of ligand (H(2)L). Interestingly, the…

LanthanideSchiff base010405 organic chemistryStereochemistryLigandMetal ions in aqueous solution[CHIM.MATE]Chemical Sciences/Material chemistry010402 general chemistry01 natural sciencesMagnetic susceptibility0104 chemical sciencesInorganic ChemistryMetalchemistry.chemical_compoundCrystallographychemistryvisual_artDiethylenetriamine[CHIM.CRIS]Chemical Sciences/Cristallographyvisual_art.visual_art_medium[CHIM]Chemical SciencesSingle crystalDalton transactions (Cambridge, England : 2003)
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Understanding and exploiting long-lived near-infrared emission of a molecular ruby

2018

Coordination chemistry reviews 359, 102 - 111 (2018). doi:10.1016/j.ccr.2018.01.004

Ligand field theory010405 organic chemistryChemistryMetal ions in aqueous solutionNear-infrared spectroscopyRelaxation (NMR)chemistry.chemical_element010402 general chemistryPhotochemistry54001 natural sciences0104 chemical sciencesInorganic ChemistryChromiumExcited stateddc:540Materials ChemistryMoleculePhotosensitizerPhysical and Theoretical Chemistry
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