Search results for "Titration"

showing 10 items of 312 documents

Influence of three types of superplasticizers on tricalciumaluminate hydration in presence of gypsum.

2006

International audience; Different types of superplasticizers have been widely used over the past few decades in order to produce a more fluid or very high strength and durable concrete. These chemical admixtures interfere with the various physico-chemical processes occurring in early cement paste. In this paper we present results from a study on the influence of superplasticizers on pure tricalciumaluminate hydration in presence of gypsum. The suspensions hydration has been investigated by conductimetry, isothermal calorimetry and total organic carbon analysis of the liquid phase. The time taken for ettringite formation has been determined without superplasticizer and in presence of three d…

Ettringite[CHIM.MATE] Chemical Sciences/Material chemistryGypsumtricalcium aluminateSuperplasticizerIsothermal titration calorimetrytricalcium aluminate.[CHIM.MATE]Chemical Sciences/Material chemistryengineering.materialCement pastechemistry.chemical_compoundsuperplasticizerAdsorptionchemistryChemical engineering[ CHIM.MATE ] Chemical Sciences/Material chemistryengineeringTricalcium aluminateDissolutionhydration
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Flecainide acetate acetic acid solvates.

2011

Flecainide acetate forms acetic acid solvates with 0.5 and 2 acetic acid molecules. Powder X-ray diffraction, differential thermal analysis/thermogravimetric, infrared, and potentiometric titration were used to determine the composition of solvates. Flecainide acetate hemisolvate with acetic acid decomposes to form a new crystalline form of flecainide acetate. This form is less stable than the already known polymorphic form at all temperatures, and it is formed due to kinetic reasons. Both flecainide acetate nonsolvated and flecainide acetate hemisolvate forms crystallize in monoclinic crystals, but flecainide triacetate forms triclinic crystals. Solvate formation was not observed when flec…

FlecainideSpectrophotometry InfraredChemistryFormic acidPotentiometric titrationPharmaceutical ScienceFlecainide AcetateMedicinal chemistryAcetic acidchemistry.chemical_compoundPropanoic acidPolymorphism (materials science)SolubilityX-Ray DiffractionThermogravimetrymedicinePotentiometrySolventsOrganic chemistryCrystallizationFlecainideAnti-Arrhythmia Agentsmedicine.drugMonoclinic crystal systemAcetic AcidJournal of pharmaceutical sciences
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Spectroscopic Methods for the Determination of Protein Interactions

2005

This unit provides guidelines on how to use steady-state fluorescence spectroscopy for the quantification of protein-protein interactions. The fluorescence of a protein is characterized by its excitation and emission spectra, quantum yield, and anisotropy. These parameters can change upon interaction with another protein and can be used to measure the extent of complex formation. The source of fluorescence can be an intrinsic fluorophore, such as tryptophan or tyrosine; a covalently attached fluorescent dye; or a fluorescent binding partner, such as a nucleotide or cofactor, that interacts specifically with the complex. Protocols are provided in this unit for determining affinity constants …

FluorophoreChemistryProteinsfood and beveragesQuantum yieldFluorescence in the life sciencesBiochemistryFluorescenceFluorescence spectroscopyProtein–protein interactionchemistry.chemical_compoundBimolecular fluorescence complementationCrystallographySpectrometry FluorescenceStructural BiologyBiophysicsTitrationProtein BindingCurrent Protocols in Protein Science
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Multicomponent polymeric micelles based on polyaspartamide as tunable fluorescent pH-window biosensors

2010

Abstract PHEA-PEG 5000 -C 16 is a polyaspartamide polymer with appended hydrophilic PEG 5000 functions and hydrophobic n-C 16 units forming biocompatible micelles with a CAC as low as 1.8 × 10 −7  M. The protonation and acidity constants of the polymer's amino and carboxylic groups have been determined by potentiometric titrations at five different concentrations higher than CAC, finding concentration-independent values. Viscosity and polarity of the micellar core have been investigated by means of fluorescent probes, finding local values comparable to those of pure toluene and to the core of sodium dodecyl sulphate micelles, independently on the protonation degree of the polymer. The fluor…

FluorophorePolymeric micelles Fluorescent biosensor PH window Self-assemblinGInorganic chemistryPotentiometric titrationBiomedical EngineeringBiophysicsProtonationBiosensing TechniquesMicellePolyethylene Glycolschemistry.chemical_compoundElectrochemistryOrganic chemistryMicellesPolyhydroxyethyl Methacrylatechemistry.chemical_classificationEquipment DesignGeneral MedicinePolymerHydrogen-Ion ConcentrationEquipment Failure AnalysisSpectrometry FluorescencechemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoPyreneSelf-assemblyPeptidesBiosensorBiotechnologyBiosensors and Bioelectronics
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Capillary electrophoresis–inductively coupled plasma-mass spectrometry hyphenation for the determination at the nanogram scale of metal affinities an…

2012

Abstract A screening strategy based on hyphenated capillary electrophoresis and inductively coupled plasma mass spectrometry (CE–ICP-MS) was developed to classify phosphorylated ligands according to their europium(III) binding affinity in a hydro-organic medium (sodium formate, pH 3.7, H2O/MeOH 90:10, v/v). Taking advantage of the high sensibility of ICP-MS for detecting phosphorus, this method enabled to assess the affinity of a variety of phosphorylated compounds, including phosphine oxides, thiophosphines, phosphonates, and phosphinates, in less than 1 h and using less than 5 ng of substance. By varying the total europium concentration, complexation constants could be determined accordin…

Formateschemistry.chemical_elementLigandsLanthanoid Series ElementsBiochemistryMass SpectrometryAnalytical ChemistryMetalchemistry.chemical_compoundCapillary electrophoresisEuropiumLimit of DetectionInductively coupled plasma mass spectrometryPrincipal Component AnalysisChromatographySodium formateMethanolOrganic ChemistryElectrophoresis CapillaryReproducibility of ResultsGeneral MedicinePhosphorus Compoundschemistryvisual_artLinear Modelsvisual_art.visual_art_mediumThermodynamicsSpectrophotometry UltravioletTitrationAbsorption (chemistry)EuropiumPhosphineJournal of Chromatography A
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Electron transfer in a supramolecular associate of a fullerene fragment

2014

Herein, we investigate the association of a fullerene fragment, hemifullerene C30H12, with an electron-donating bowl-shaped tetrathiafulvalene derivative (truxTTF). UV/Vis titrations and DFT calculations support formation of the supramolecular complex, for which an association constant of log Ka = 3.6±0.3 in CHCl3 at room temperature is calculated. Remarkably, electron transfer from truxTTF to C30H12 to form the fully charge-separated species takes place upon irradiation of the associate with light, constituting the first example in which a fullerene fragment mimics the electron-accepting behavior of fullerenes within a supramolecular complex.

Fullerene chemistryFullereneStereochemistrySupramolecular chemistryGeneral ChemistryCatalysisPhotoinduced electron transferchemistry.chemical_compoundElectron transferCrystallographychemistryTitrationDerivative (chemistry)Tetrathiafulvalene
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Conjugated Porphyrin Dimers: Cooperative Effects and Electronic Communication in Supramolecular Ensembles with C60

2016

International audience; Two new conjugated porphyrin-based systems (dimers 3 and 4) endowed with suitable crown ethers have been synthesized as receptors for a fullerene-ammonium salt derivative (1). Association constants in solution have been determined by UV–vis titration experiments in CH2Cl2 at room temperature. The designed hosts are able to associate up to two fullerene-based guest molecules and present association constants as high as ∼5 × 108 M–1. Calculation of the allosteric cooperative factor α for supramolecular complexes [3·12] and [4·12] showed a negative cooperative effect in both cases. The interactions accounting for the formation of the associates are based, first, on the …

Fullerene010405 organic chemistryStereochemistrySupramolecular chemistryQuímica orgánicaEtherGeneral ChemistryConjugated system010402 general chemistry01 natural sciencesBiochemistryPorphyrinCatalysis3. Good health0104 chemical scienceschemistry.chemical_compoundCrystallographyColloid and Surface ChemistrychemistryMoleculeTitration[CHIM.COOR]Chemical Sciences/Coordination chemistryDerivative (chemistry)
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Bis(imidazolium) salts derived from amino acids as receptors and transport agents for chloride anions

2015

The binding properties of bis(imidazolium) hosts 1a–c derived from amino acids towards different anions have been studied by 1H NMR titration experiments in 95 : 05 CD3CN : H2O at 303 K, ESI-MS and theoretical calculations. Among this family, the salt 1c showed a strong and high selectivity for chloride anions. Transmembrane chloride transport activity has also been studied for the three bis(imidazolium) based transporters in POPC liposome models, and compound 1a was identified as an active chloride/nitrate exchanger.

General Chemical EngineeringChemistry OrganicSalt (chemistry)Medicinal chemistryChlorideCompostos orgànics Síntesichemistry.chemical_compoundmedicineLife ScienceOrganic chemistryPOPCVLAGchemistry.chemical_classificationLiposomeamino acidsOrganic Chemistrychloride anionsQuímica orgánicaGeneral ChemistryOrganische ChemieTransmembrane proteinAmino acidchemistryProton NMRbis(imidazolium)TitrationAminoàcidsmedicine.drug
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Thermodynamic Parameters for the Protonation of Poly(allylamine) in concentrated LiCl(aq) and NaCl(aq)

2004

The acid-base properties of poly(allylamine) (MW ) 15 kDa) were determined by potentiometry and calorimetry in aqueous solutions at t ) 25 °C. Potentiometric measurements were carried out in a wide range of ionic strengths (0.1 e I/molâL-1 e 5.0) in NaCl(aq) and LiCl(aq), while enthalpy changes for the protonation of poly(allylamine) were determined by calorimetry in the same ionic strength range but only in NaCl(aq). Analysis of the experimental data was carried out using two different models: the first based on a modified Henderson-Hasselbalch two parameter equation and the second on the three parameter equation proposed by Ho¨gfeldt. Protonation constants are given for both models and io…

General Chemical EngineeringEnthalpyPotentiometric titrationInorganic chemistryIonic bondingProtonationGeneral ChemistryCalorimetryProtonationPoly(allylamine)Allylaminechemistry.chemical_compoundchemistrySpecific ion interaction theoryspeciationIonic strengthPhysical chemistrySettore CHIM/01 - Chimica Analitica
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Bisferrocenyl-functionalized pseudopeptides: access to separated ionic and electronic contributions for electrochemical anion sensing

2016

Pseudopeptidic receptors containing ferrocene fragments have been prepared and their response to a series of anions was measured by a voltammetry of microparticles methodology. Such water-insoluble compounds yield anion-assisted reversible solid-state oxidations differing in their open-circuit potential and their midpeak potential recorded in cyclic voltammetric measurements. The difference between those potentials provides the individual thermodynamic contributions of electron and proton transfer, revealing that the mechanism of an ion-sensitive electrode can differ in potentiometry and voltammetry. The studied receptors are potentially interesting for potentiometric sensing, showing relat…

General Chemical EngineeringInorganic chemistryPotentiometric titrationIonic bonding02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyElectrochemistry01 natural sciences0104 chemical sciencesIonchemistry.chemical_compoundFerrocenechemistrypseudopeptidespotentiometric sensingYield (chemistry)Electrodeelectrochemical anion sensing0210 nano-technologyVoltammetry
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