Search results for "ionic strength"

showing 10 items of 198 documents

Aggregation Processes and Formation of Silico-calco-alkaline Gels under High Ionic Strength

2002

This paper presents a systematic in situ study of the process of formation of silico-calco-alkaline gels starting from a liquid colloidal solution containing different alkaline ions and different calcium concentration until the final gel state. The combined use of X-ray and neutron small-angle scattering (SAS) and dynamical rheometry techniques lead to a consistent description of the structure of the aggregates and of the mechanisms of aggregation involved in gel formation. SAS results indicate that the aggregates are fractal objects, their structure strongly depending on calcium ion concentration. The differences in gelation kinetics for systems containing different alkaline ions were attr…

chemistry.chemical_classificationRheometryKineticsInorganic chemistryConcentration effectFractal dimensionSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonCondensed Matter::Soft Condensed MatterBiomaterialsColloid and Surface ChemistrychemistryChemical engineeringIonic strengthMoleculeCounterionJournal of Colloid and Interface Science
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Study of silica-structured materials as sorbents for organophosphorus pesticides determination in environmental water samples

2018

Abstract A novel sorbent based on a UVM-7 mesoporous silica doped with Ti has been synthesized and used for solid-phase extraction of several organophosphorus pesticides in environmental water samples followed by gas chromatography coupled to a nitrogen-phosphorus selective detector. Thus, mesoporous silica materials doped with Ti and Fe as well as immobilized cyclodextrin silica-based supports were prepared and morphologically characterized by several techniques such as transmission electronic microscopy, nitrogen adsorption-desorption and X-ray diffraction. These sorbents were comparatively evaluated, and Ti25-UVM-7 material was selected as the best solid phase. After optimization of extr…

chemistry.chemical_classificationSorbentChromatographyCyclodextrinChemistry010401 analytical chemistryExtraction (chemistry)02 engineering and technologyMesoporous silica021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAnalytical ChemistryColumn chromatographyIonic strengthGas chromatographySolid phase extraction0210 nano-technologyTalanta
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Layer-by-layer deposited multilayer assemblies of polyelectrolytes and proteins: from ultrathin films to protein arrays

2008

We have recently introduced a new method of creating ultrathin films of polyelectrolytes based on the electrostatic attraction between opposite charges. Multilayer assemblies are adsorbed in a layer-by-layer fashion from aqueous solutions of the polymers. The total film thickness can easily be adjusted by varying the ionic strength of the solution. Here, we report on the temperature stability and the water content of the multilayer assemblies. Furthermore, we have extended our concept to the incorporation of protein layers into films of synthetic polyelectrolytes. The well established system biotin/streptavidin was used to construct such multilayers, also by biospecific recognition. Adsorpt…

chemistry.chemical_classificationStreptavidinMaterials scienceSmall-angle X-ray scatteringLayer by layerAnalytical chemistryPolymerPolyelectrolytechemistry.chemical_compoundchemistryChemical engineeringIonic strengthSelf-assemblyFourier transform infrared spectroscopy
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Salt effects on the protonation of l-histidine and l-aspartic acid: a complex formation model

1991

Abstract Protonation constants of l -histidine (histidinate: his − ) and l -aspartic acid (aspartate: asp 2− ) were determined potentiometrically, using the (H + ) glass electrode, in aqueous tetraethylammonium iodide (Et 4 NI), calcium chloride and sodium chloride solutions, at 0 −3 and 10 ⩽, T ⩽, 45 ° C. Differences in protonation constants determined in different salt media were explained by a complex formation model and, according to this model, the presence of the following species was hypothesized: Ca(his) + , CaH(his) 2+ , CaH 2 (his) 3+ Na(his) 0 , H 3 (his)X + , H 2 (his)X 0 , Et 4 N(his) 0 , Et 4 NH(his) + , Ca(asp) 0 , CaH(asp) + , CaH 2 (asp) 2+ , Na(asp) − , NaH(asp) 0 , H 3 (a…

chemistry.chemical_classificationTetraethylammonium iodideAqueous solutionendocrine system diseasesSodiumInorganic chemistrychemistry.chemical_elementProtonationCondensed Matter PhysicsMedicinal chemistrychemistry.chemical_compoundDicarboxylic acidchemistryIonic strengthAspartic acidPhysical and Theoretical ChemistryInstrumentationHistidineThermochimica Acta
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Kinetics in a Double Antibody Radioimmunoassay (RIA): Diffussion Control

2012

Competitive protein binding radioimmunoassay (CPB-RIA) is a principal method for quantifying serum C Peptide concentration. The accuracy of this method is critically dependent on factors that influence the reaction between anti-C Peptide antibody (P) with 125I-C Peptide (M). We studied the influence of initial concentration of M, ionic strength, and viscosity on the reaction between M and P. A kinetic model for the the reaction between. Such model adjusts satisfac- torily to the results. Bi-exponential and irreversible kinetics is determined. The results of the viscosity analysis show clear negative influence on the direct reaction rate. The ionic strength shows scarce influence on equilibr…

chemistry.chemical_classificationViscosityReaction rate constantChromatographychemistryIonic strengthAutomotive EngineeringKineticsAnalytical chemistryPeptideRadioimmunoassayDielectricEndothermic processAmerican Journal of Chemistry
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Speciation of trialkyltin(IV) cations in natural fluids

2004

The hydrolysis of (CH(3))(3)Sn(+), (C(2)H(5))(3)Sn(+) and (C(3)H(7))(3)Sn(+) has been studied in a Synthetic Seawater (SSW) ionic medium simulating the major composition of natural seawater, at different salinities (5 less than or equal to S less than or equal to 45), and at t = 25 degreesC. Interactions with anionic components of SSW, considered as single sea salt, are determined by means of a complex formation model. By potentiometric measurements (ISE-H(+) and ISE-F(-) electrodes), the model has been extended to also consider interactions of organotins with carbonate and fluoride ions, which are other important components of seawater. Literature and new values of hydrolysis constants in …

chemistry.chemical_classificationfood.ingredientChemistryHydrolysisSea saltmedia_common.quotation_subjectInorganic chemistryIonic bondingArtificial seawaterSalt (chemistry)General ChemistryOceanographytrialkyltin(IV)SpeciationHydrolysisfoodIonic strengthEnvironmental ChemistrySeawaterIonic strength Protonation protonation constantsHydrolysis; trialkyltin(IV); Natural FluidsNatural FluidsWater Science and Technologymedia_commonMarine Chemistry
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On the Complexation of Cu(II) and Cd(II) With Polycarboxyl Ligands. Potentiometric Studies With ISE-H+, ISE-Cu2+, and ISE-Cd2+

2009

The interaction of Cu2+ and Cd2+ ions with polyacrylates (PAA, 2 kDa and 100 kDa), polymetacrylate(PMA, 5.4 kDa), and alginate (AA, 70 kDa to 100 kDa) was studied by potentiometry, using ISE-Cu2+, ISE-Cd2+, and ISE-H+ electrodes. The investigations were performed in NaNO3 aqueous solutions, in the ionic strength range 0.10 e I (mol ·L-1) e 0.75, at T ) 298.15 K. The “diprotic-like model” was used to explain the acid-base behavior of the polycarboxylates under investigation (for this model, the monomeric unit of the polyelectrolyte is considered as a dicarboxylate). The results give evidence for the formation of the ML species in all the systems investigated. In addition, the MLH species was…

inorganic chemicalsAcrylate polymerchemistry.chemical_classificationSequestering abilitypolycarboxylic acidsLigandGeneral Chemical EngineeringIonic strength dependencePotentiometric titrationInorganic chemistryGeneral ChemistryUronic acidComplexation Potentiometric study polyelectrolytesPolysaccharidePolyelectrolytechemistry.chemical_compoundchemistryIonic strengthSodium nitrateSettore CHIM/01 - Chimica Analiticapolycarboxylic acids; Sequestering ability; Ionic strength dependenceNuclear chemistryJournal of Chemical & Engineering Data
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Incorporation of dynamic boronate links and Ag nanoparticles into PVA hydrogels for pH-Regulated and prolonged release of methotrexate

2021

Abstract In this study, pH-responsive hydrogels based on PVA-boronate crosslinks were prepared via a simple route and used for controlled and targeted delivery of anticancer drug methotrexate. A double network (DN) hydrogel composed of didiol-boronate/PVA complex as the first network and PVA crystallites generated by a freeze-thaw process as the second one was developed. The swelling of PVA-boronate DN hydrogels demonstrated high sensitivity to multiple stimuli including the pH, temperature, and ionic strength of the media thanks to the dynamic boronate links in the first network. Moreover, unlike previously reported hydrogels based on the boronate linkages, the new DN hydrogels preserved t…

inorganic chemicalsChemistrytechnology industry and agricultureCancer therapyPharmaceutical ScienceAg nanoparticlesmacromolecular substances02 engineering and technology021001 nanoscience & nanotechnologycomplex mixtures030226 pharmacology & pharmacyAnticancer drug03 medical and health sciences0302 clinical medicineChemical engineeringProlonged releaseIonic strengthSelf-healing hydrogelsmedicineMethotrexateSwellingmedicine.symptom0210 nano-technologymedicine.drugJournal of Drug Delivery Science and Technology
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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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Thermodynamic Study For The Protonation Of Halloysite

2016

The Halloysite (Al2Si2O5(OH)4·2H2O) is an abundant and cheap clay and is considered one of the most promising nano structured and naturally occurring clay mineral. Large deposits of this material are present in France, Belgium, China, New Zealand and USA [1,2]. Among the spheroidal, tubular or platy morphologies, the tubular is the most common and abundant one. Typically, halloysite nanotubes (HNTs) are formed by 15 – 20 aluminosilicate layers, having a length of 1 ± 0.5 μm, and inner and outer diameters of 10 – 15 nm and 50 -70 nm, respectively [1]. In each layer, the SiOH and the AlOH groups are disposed on the external and the internal surfaces, respectively. As consequence, in each nano…

ionic strength.protonation constantspeciationacid-bsae propertieHalloysiteSettore CHIM/01 - Chimica Analitica
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