Search results for "chimica"

showing 10 items of 4450 documents

Sequestration of organometallic compounds by natural organic matter. binding of trimethyltin(IV) by fulvic and alginic acids

2006

The binding capacity of fulvic and alginic acids towards trimethyl tin(IV) cation was quantitatively determined in order to evaluate the sequestering ability of toxic organometallic compounds by natural organic matter. Investigations were performed in the pH range of natural waters (5–8.5) where the carboxylate groups, largely present in both sequestering agents, are the main binding sites. A chemical interaction model, according to which both the protonation of polyelectrolyte ligands and the hydrolysis of the organotin cation in NaCl aqueous solution were considered, was used to define the speciation of the systems under investigation. Measurements performed at different ionic strength va…

Aqueous solutionChemistrycomplexationInorganic chemistrysequestrationProtonationGeneral ChemistryPolyelectrolyteInorganic ChemistryHydrolysischemistry.chemical_compoundspeciationIonic strengthStability constants of complexesSettore CHIM/01 - Chimica AnaliticaCarboxylatenatural organic matterorganometallic compoundhuman activitiesAlginic acidApplied Organometallic Chemistry
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Use of SPME extraction to determine organophosphorus pesticides adsorption phenomena in water and soil matrices

2005

Solid-phase micro extraction (SPME) coupled with GC enables rapid and simple analysis of organophosphorus pesticides in a range of complex matrices. Investigations were made into the extraction efficiencies from water of six organophosphorus insecticides (methamidophos, omethoate, dimethoate, parathion methyl, malathion, and parathion ethyl) showing a wide range of polarities. Three SPME fibres coated with different stationary phases, polydimethylsiloxane, polyacrylate, and carbowax-divinylbenzene (CW-DVB), were investigated. Water was spiked with the pesticides at concentrations from 1 to 0.01 µg mL-1, and the solutions used for optimization of the procedure. The CW-DVB fibre, with a 65 µm…

Aqueous solutionChromatographyHealth Toxicology and MutagenesisMethamidophosSettore AGR/13 - Chimica AgrariaExtraction (chemistry)Public Health Environmental and Occupational HealthSoil SciencePesticidePollutionAnalytical Chemistrychemistry.chemical_compoundAdsorptionParathionchemistryParathion methylSPME Organophosphorus insecticides Water SoilEnvironmental ChemistryOmethoateWaste Management and DisposalWater Science and TechnologyInternational Journal of Environmental Analytical Chemistry
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Sequestration of alkyltin(IV) cations by complexation with amino-polycarboxylic chelating agents

2013

Abstract The binding capacity of four amino-polycarboxylic ligands (APCs) [nitrilotriacetate (NTA), ethylenediamine- N , N , N′ , N′ -tetraacetate (EDTA), (S,S)-ethylenediamine- N , N ′-disuccinic acid (S,S-EDDS) and diethylenetriamine- N , N , N′ , N″ , N″ -pentaacetate (DTPA)] towards mono-, di- and tri-alkyltin(IV) cations [(CH 3 )Sn 3 + , (CH 3 ) 2 Sn 2 + , (C 2 H 5 ) 2 Sn 2 + , (CH 3 ) 3 Sn + or (C 2 H 5 ) 3 Sn + ] was studied, in aqueous solutions, by ISE-H + potentiometry, at I  = 0.1 mol L − 1 (NaCl) and at T  = 298.15 K. In all the systems R x Sn (4 − x)+  − APC (R = CH 3 or C 2 H 5 ) a strong 1:1 species is formed together with protonated, hydroxo and dinuclear complexes. The valu…

Aqueous solutionComplexation in aqueous solutionStereochemistryLigandEthylenediamineProtonationAlkyltin(IV) cations; Amino-polycarboxylic ligands; Complexation in aqueous solution; Sequestration ability of complexones;Condensed Matter PhysicsMedicinal chemistryAtomic and Molecular Physics and OpticsAlkyltin(IV) cationElectronic Optical and Magnetic MaterialsIonAmino-polycarboxylic ligandchemistry.chemical_compoundSequestration ability of complexoneschemistryDiethylenetriamineMaterials ChemistryChelationSettore CHIM/01 - Chimica AnaliticaPhysical and Theoretical ChemistrySimple correlationSpectroscopy
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[2]Catenanes and inclusion complexes derived from self-assembled rectangular PdII and PtII metallocycles

2012

New inclusion complexes and [2]catenanes were self-assembled from a fluorescent diazapyrenium based ligand, a PdII or PtII complex, and cyclic or acyclic electron rich aromatic guests in aqueous and organic media. The molecular rectangles display a π-deficient cavity suitable to incorporate π-donor aromatic systems. The inclusion complexes between the metallocycles and phenylenic (2a,b) and naphthalenic (3a,b–5a,b) derivatives were studied by NMR, UV-vis and fluorescence spectroscopy. The crystal structure of (3b) ⊂ 1a·6PF(6) confirmed the insertion of the guest into the cavity of the metallocycle. Following the same self-assembly strategy, the use of polyethers 6,7 as π-donors resulted in …

Aqueous solutionLigandChemistryStereochemistryCatenaneCrystal structureSettore CHIM/06 - Chimica OrganicaMetallacycleFluorescenceFluorescence spectroscopySelf assembledCatenanes inclusion complexes PdII PtII metallocyclesInorganic ChemistryCrystallographySettore CHIM/03 - Chimica Generale E Inorganica
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Palladium(II) Complexes of Aminopolycarboxylic Ligands in Aqueous Solution

2011

Thebindingcapacityof fiveaminopolycarboxylicligands(APCs)(nitrilotriacetate(NTA),ethylenediamine-N,N,N 0 , N 0 -tetraacetate (EDTA), (S,S)-ethylenediamine-N,N 0 -disuccinic acid (S,S-EDDS), diethylenetriamine-N,N,N 0 ,N 00 ,N 00 -pentaacetate (DTPA), and triethylenetetraamine-N,N,N 0 ,N 00 ,N 000 ,N 000 -hexaacetate (TTHA)) toward the palladium(II) ion was studied by potentiometric titrations (ISE-H + electrode) in NaNO3 and in NaClO4/NaI (at different molar ratios) solutions and by spectrophotometric titrations (only in NaClO4), at I = 0.1 mol 3 kg � 1 and at T = 298.15 K. The high stability of Pd 2+ -complexones species inhibits the formation of sparingly soluble hydroxo species until pH …

Aqueous solutionLigandcomplexoneGeneral Chemical EngineeringPotentiometric titrationInorganic chemistryPalladium(II)chemistry.chemical_elementcomplexeProtonationsequestrationGeneral ChemistryIonchemistry.chemical_compoundEDDSchemistryTitrationSettore CHIM/01 - Chimica Analiticaaqueous solutionPalladiumNuclear chemistry
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Interaction of methyltin(IV) compounds with carboxylate ligands. Part 2: Formation thermodynamic parameters, predictive relationships and sequesterin…

2008

Thermodynamic data of mono-, di- and tri-methyltin(IV)-carboxylate complexes (acetate, malonate, succinate, oxydiacetate, diethylenetrioxydiacetate, malate, citrate, 1,2,3-tricarballylate, 1,2,3,4-butanetetracarboxylate, 1,2,3,4,5,6-benzenehexacarboxylate) in aqueous solution are reported at t = 25 °C and I = 0 mol l−1. Thermodynamic parameters obtained were analysed to formulate empirical predictive relationships as a function of different parameters, such as the number of carboxylate groups of the ligand and the charge of the alkyltin(IV) cation. Sequestration diagrams of citrate and 1,2,3-tricarballylate towards alkyltin(IV) cations at different pH values are also reported and discussed.…

Aqueous solutionLigandempirical relationshipInorganic chemistrymethyltin(IV) complexeGeneral ChemistryCalorimetryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundspeciation in aqueous solutionMalonatechemistrythermodynamic parameterSettore CHIM/01 - Chimica AnaliticaCarboxylatethermodynamic parametersempirical relationshipsmethyltin(IV) complexes; thermodynamic parameters; calorimetry; empirical relationships; speciation in aqueous solutionmethyltin(IV) complexescalorimetry
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GROWTH AND PHOTOELECTROCHEMICAL BEHAVIOUR OF ELECTRODEPOSITED ZnO THIN FILMS FOR SOLAR CELLS

2012

Thin zinc oxide films were deposited potentiostatically from zinc nitrate aqueous solutions on ITO substrates. The influence of experimental parameters (temperature, electrolyte concentration, deposition potential) on structure and morphology of films was investigated. Deposited films were generally polycrystalline in structure, even if growth according to preferential planes occurs in certain conditions. The effect of thermal treatments in air at 150 and 350 °C was also studied. In some cases, Cl species were incorporated into deposit by adding zinc chloride to the electrolyte. A photoelectrochemical investigation, performed in neutral solution before and after thermal treatment, gives mor…

Aqueous solutionMaterials scienceAnnealing (metallurgy)General Chemical EngineeringInorganic chemistryOxidechemistry.chemical_elementElectrolyteThermal treatmentZincchemistry.chemical_compoundSettore ING-IND/23 - Chimica Fisica ApplicatachemistryZinc nitrateMaterials ChemistryElectrochemistryThin filmZnO CIGS Solar Cells Electrodeposition TCO
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Halloysite nanotubes filled with MgO for paper reinforcement and deacidification

2021

Abstract A novel material for the deacidification and protection of paper has been designed by using MgO filled halloysite nanotubes (Hal). The ability of MgO loaded nanotubes to control the acidic conditions was evaluated by pH measurements in aqueous solvent. Afterwards, paper was impregnated into hydroxypropyl cellulose dispersions containing the consolidating material. A simulation of strong acidic conditions allowed us to evaluate the deacidification effect of the composite material on the samples. In particular, the paper reaches a pH of 7.7 after 1 h exposition to HNO3 vapours when MgO-Hal nanoparticles are added to the impregnation mixture at a concentration of 10 wt% and it remains…

Aqueous solutionMaterials scienceHydroxypropyl celluloseHalloysite nanotubesNanoparticleGeologyDynamic mechanical analysisengineering.materialDMAHydroxypropyl cellulosemedicine.diseaseHalloysitechemistry.chemical_compoundchemistryChemical engineeringGeochemistry and PetrologyDeacidificationUltimate tensile strengthmedicineengineeringCelluloseCelluloseVapoursPaper consolidationSettore CHIM/02 - Chimica Fisica
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Fabrication of metal nano-structures using anodic alumina membranes grown in phosphoric acid solution: Tailoring template morphology

2007

Abstract The influence of experimental parameters on the morphology of the porous structure and on the formation kinetics has been investigated for anodic alumina membranes (AAM) grown in aqueous H 3 PO 4 at 160 V. It was found that pore aspect ratio and membrane porosity on the solution-side surface are influenced by tensiostatic charge, bath temperature and the presence of Al 3+ ions in solution. Morphological and kinetic data, recorded in different conditions, give useful information on the growth mechanism of pore channels in phosphoric acid solution. Nickel nano-structures have been fabricated using AAM as template. Electroless deposition, performed by adding the reducing agent to a su…

Aqueous solutionMaterials scienceMetal ions in aqueous solutionNanowireGeneral Physics and AstronomyAlumina membraneNanotechnologySurfaces and InterfacesGeneral ChemistryCondensed Matter PhysicsSurfaces Coatings and FilmsNanowirechemistry.chemical_compoundSettore ING-IND/23 - Chimica Fisica ApplicataMembraneElectrodepositionChemical engineeringchemistryTransition metalNickelNano-PorosityPhosphoric acidApplied Surface Science
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Electrochemical conversion of pressurized CO2 at simple silver-based cathodes in undivided cells: study of the effect of pressure and other operative…

2020

Abstract Electrochemical reduction of pressurized CO2 is proposed as an interesting approach to overcome the main hurdle of the CO2 electrochemical conversion in aqueous solution, its low solubility (ca. 0.033 M), and to achieve good faradaic efficiency in CO using simple sheet silver cathodes and undivided cells, thus lowering the overall costs of the process. The effect on the process of CO2 pressure (1–30 bar), current density, nature of the supporting electrolyte and other operative conditions, such as the surface of the cathode or the mixing rate, was studied to enhance the production of CO. It was shown that pressurized conditions allow to improve drastically the current efficiency o…

Aqueous solutionMaterials scienceSilverSupporting electrolyteGeneral Chemical EngineeringSettore ING-IND/27 - Chimica Industriale E TecnologicaElectrochemistryCathodelaw.inventionChemical engineeringlawElectrodeMaterials ChemistryElectrochemistryPressureCO2SolubilityCarbon monoxideCurrent densityFaraday efficiencyReduction
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