Search results for "Metal ions in aqueous solution"

showing 6 items of 256 documents

Preparation of polyelectrolyte-modified membranes for heavy metal ions removal

2017

ABSTRACTPolyethersulfone membranes were modified by polyelectrolyte (PE) multilayers, made of poly(allylamine hydrochloride) with poly(styrene sulfonate), to remove Cu2+, Zn2+ and Ni2+ heavy metal cations from aqueous solutions in a wide range of metal concentration (50–1200 ppm). After characterization of the modified membranes, the efficiency of the process was estimated for single heavy metal ions solution leading to high rejection rates (>90% for 50 ppm) and good adsorption capacities (7.0–8.5 mg cm−2) whatever the metal ion tested. The stability in time of the modified membranes was proved by repeating successive filtrations with the same membrane. The filtration process was also used …

inorganic chemicalsMetal ions in aqueous solutionInorganic chemistryUltrafiltration02 engineering and technology010402 general chemistry01 natural sciencesWater PurificationMetalchemistry.chemical_compoundAdsorptionCationsMetals HeavyEnvironmental Chemistry[CHIM]Chemical SciencesWaste Management and DisposalComputingMilieux_MISCELLANEOUSWater Science and TechnologyIonsAqueous solutionChemistryGeneral Medicine021001 nanoscience & nanotechnologyPolyelectrolytesPolyelectrolyte0104 chemical sciencesSulfonateMembranevisual_artvisual_art.visual_art_mediumAdsorption0210 nano-technologyFiltration
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Inorganic nanomaterials in the aquatic environment: behavior, toxicity, and interaction with environmental elements

2016

AbstractThe aim of this paper is to present characteristics, toxicity and environmental behavior of nanoparticles (NPs) (silver, copper, gold, zinc oxide, titanium dioxide, iron oxide) that most frequently occur in consumer products. In addition, NPs are addressed as the new aquatic environmental pollutant of the 21stcentury. NPs are adsorbed onto particles in the aquatic systems (clay minerals, fulvic and humic acids), or they can adsorb environmental pollutants (heavy metal ions, organic compounds). Nanosilver (nAg) is released from consumer products into the aquatic environment. It can threaten aquatic organisms with high toxicity. Interestingly, copper nanoparticles (Cu-NPs) demonstrate…

inorganic chemicalsPollutionlcsh:Environmental protectionmedia_common.quotation_subjectMetal ions in aqueous solutionchemistry.chemical_element02 engineering and technologyZinc010501 environmental sciences01 natural sciencesnanosilverchemistry.chemical_compoundAdsorptionpollutionlcsh:TD169-171.8nanocoppernanomaterials0105 earth and related environmental sciencesmedia_commonPollutantAquatic ecosystemtechnology industry and agriculturetoxicityGeneral Medicineaquatic environmental021001 nanoscience & nanotechnologychemistryIonic strengthEnvironmental chemistryTitanium dioxide0210 nano-technologyArchives of Environmental Protection
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Mass spectrometric studies on pyridine-piperazine-containing ligands and their complexes with transition metals formed in solution.

2001

Electrospray ionization (ESI) and matrix-assisted laser desorption/ionization (MALDI) methods were used to study open-chain piperazine-containing ligands (L) and their complexes formed with transition-metal salts. ESI and MALDI measurements were performed with a Fourier transform ion cyclotron resonance (FT-ICR) and a time-of-flight (TOF) mass spectrometer, respectively. Only singly charged complexes, between one ligand and one or several metal ions, were formed in the ESI measurements. Because the net charge was always one, one or several counterions were attached to the complex. Under ESI conditions, the complexes formed between the ligands and metal (Co, Ni, Cu, and Cd) salts were [L + M…

inorganic chemicalschemistry.chemical_classificationCollision-induced dissociationLigandMetal ions in aqueous solutionElectrospray ionizationOrganic ChemistryAnalytical chemistryMass spectrometryFourier transform ion cyclotron resonanceAnalytical ChemistrychemistryPolymer chemistryQualitative inorganic analysisCounterionSpectroscopyRapid communications in mass spectrometry : RCM
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From isolated 1H-pyrazole cryptand anion receptors to hybrid inorganic-organic 1D helical polymeric anion receptors

2015

We report a novel 1-D helical coordination polymer formed by protonated polyamine 1H-pyrazole cryptands interconnected by Cu2+ metal ions that are able to encapsulate anionic species behaving as a multianion receptor. Switching from a monomeric receptor to a polymeric receptor is activated by metal ions and pH.

kemiaChemistryStereochemistryCoordination polymerMetal ions in aqueous solutionCryptandreceptorsProtonationPyrazolechemistryInorganic Chemistrychemistry.chemical_compoundMonomerPolymer chemistryPolyamineReceptorta116Dalton Transactions 44: 7761-7764 (2015)
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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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Interaction of methyltin(IV) compounds with carboxylate ligands. Part 1: formation and stability of methyltin(IV)–carboxylate complexes and their rel…

2006

Quantitative data on the stability of mono-, di- and trimethyltin(IV)-carboxylate complexes (acetate, malonate, succinate, malate, oxydiacetate, diethylenetrioxydiacetate, tricarballylate, citrate, butanetetracarboxylate and mellitate) are reported at t=25°C and I → 0 mol l - 1 . Several mononuclear, mixed proton, mixed hydroxo and polynuclear species are formed in these systems. As expected, the stability trend is mono- > di- > trimethyltin(IV) and mono < di < tri < tetra < hexa for the organotin moieties and carboxylate ligands investigated, respectively. Moreover, ligands containing, in addition to carboxylic,-O-and-OH groups show a significantly higher stability with respect to analogou…

methyltin(IV) cationLigandStereochemistryMetal ions in aqueous solutionGeneral ChemistryHEXAMedicinal chemistryInorganic Chemistrymethyltin(IV)–carboxylate complexeschemistry.chemical_compoundMalonatechemistryspeciationStability constants of complexesmethyltin(IV) cationsChemical stabilitySettore CHIM/01 - Chimica AnaliticaCarboxylatemethyltin(IV)–carboxylate complexeBinding sitecarboxylate ligandmethyltin(IV) cations; carboxylate ligands; methyltin(IV)–carboxylate complexes; speciationcarboxylate ligands
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