Search results for "CONSTANT"

showing 10 items of 1718 documents

Enseñanza de las ciencias : revista de investigación y experiencias didácticas

1996

Resumen basado en el de la publicación Resumen en inglés La evolución histórica del principio de Le Chatelier está relacionada con su uso en el aula de química. La aparente simplicidad en la cual el principio de Le Chatelier fue formulado por primera vez y el éxito logrado en la implementación de algunos procesos industriales importantes le dio un reconocimiento inicial que aún perdura. Sin embargo, desde el comienzo de este siglo, diferentes autores han señalado el carácter limitado de la regla cualitativa y su formulación vaga y ambigua. Además, la termodinámica dada por el Principio de Le Chatelier en algunas formulaciones cuantitativas limitan su aplicabilidad. Sin embargo, la mayoría d…

epistemologíaEquilibri dinàmicmedia_common.quotation_subjectPhilosophyQuímicaLa llei del desplaçament de l'equilibri químicpráctica pedagógicaestudios científicosEducationLe Chatelier's principleReaccions químiquesCiència Ensenyamentformación de profesoresFormulació matemàtica de De Donder y Rysselberguehistoria de la educaciónCalculusPrincipio de Le ChatelierSimplicityConstant (mathematics)Mathematical economicsmedia_commonFormació del professorat
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Enhancement of Hydrolysis through the Formation of Mixed Heterometal Species: Al3+/CH3Sn3+ Mixtures

2013

ABSTRACT: The hydrolysis of mixed-metal cations (Al3+/CH3Sn3+) was studied in aqueous solutions of NaNO3, at I = 1.00 ± 0.05 mol·dm−3 and T = 298.15 K, by potentiometric technique. Several hydrolytic mixed species are formed in this mixed system, namely, Alp(CH3Sn)q(OH)r with (p, q, r) = (1, 1, 4), (1, 1, 5), (1, 1, 6), (2, 1, 4), (1, 2, 5), (1, 4, 11), (1, 3, 8), and (7, 6, 32). The stability of these species, expressed by the equilibrium: pAl3+ + qCH3Sn3+ + rOH− = Alp(CH3Sn)q(OH)r 3(p+q)−r, βpqr OH, can be modeled by the empirical relationship: log βpqr OH = −3.34 + 2.67p + 9.23(q + r). By using the equilibrium constant Xpqr relative to the formation reaction: pAl(p+q)(OH)r + q(CH3Sn)(p+q…

equilibrium analysiequilibrium analysis; mixed hydrolysis of metal ions; aluminium(III); monomethyltin(IV)monomethyltin(IV)Aqueous solutionChemistryStereochemistryGeneral Chemical EngineeringPotentiometric titrationEmpirical relationships Formation reaction Mixed species Mixed systems Potentiometric techniqueGeneral ChemistryPotentiometric techniqueMedicinal chemistryTurn (biochemistry)HydrolysisMixed systemsMixed speciesMixed systemsMixed speciesEmpirical relationshipsSettore CHIM/01 - Chimica AnaliticaSolubilityaluminium(III)mixed hydrolysis of metal ionFormation reactionEquilibrium constantJournal of Chemical & Engineering Data
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The Born–Oppenheimer equilibrium bond distance of GeO from millimetre- and submillimetre-wave spectra and quantum-chemical calculations

2014

The millimetre- and submillimetre-wave spectra of the five common isotopologues of (GeO)-O-16 in their electronic and vibrational ground state have been recorded in the spectral region 115-732GHz; for (GeO)-Ge-74-O-16, the rotational spectrum in the v = 1 state has been detected as well. Exploiting the high precision of the measurements, the Born-Oppenheimer breakdown parameter Delta(Ge)(01) could be determined from a Dunham analysis of the spectral data, whereas Delta(O)(01) was obtained from quantum-chemical calculations, because of the lack of high-precision measurements for the (GeO)-O-18 isotopologues. From the rotational equilibrium constant, the Born-Oppenheimer equilibrium distance …

equilibrium bond distanceBorn-Oppenheimer breakdownrotational spectrumChemistryBiophysicsBorn–Oppenheimer approximationCondensed Matter PhysicsSpectral linequantum-chemical calculationBond lengthsymbols.namesakeRotational spectrumsymbolsMillimeterIsotopologuePhysical and Theoretical ChemistryAtomic physicsGround stateMolecular BiologyAstrophysics::Galaxy AstrophysicsEquilibrium constant
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Poincaré Type Inequalities for Vector Functions with Zero Mean Normal Traces on the Boundary and Applications to Interpolation Methods

2019

We consider inequalities of the Poincaré–Steklov type for subspaces of H1 -functions defined in a bounded domain Ω∈Rd with Lipschitz boundary ∂Ω . For scalar valued functions, the subspaces are defined by zero mean condition on ∂Ω or on a part of ∂Ω having positive d−1 measure. For vector valued functions, zero mean conditions are applied to normal components on plane faces of ∂Ω (or to averaged normal components on curvilinear faces). We find explicit and simply computable bounds of constants in the respective Poincaré type inequalities for domains typically used in finite element methods (triangles, quadrilaterals, tetrahedrons, prisms, pyramids, and domains composed of them). The second …

estimates of constants in functional inequalitiesvektorit (matematiikka)interpolointiPoincaré type inequalitiesinterpolation of functionsfunktiot
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Tuning the Electrochemistry of Free-Base Porphyrins in Acidic Nonaqueous Media: Influence of Solvent, Supporting Electrolyte, and Ring Substituents

2016

International audience; A detailed study of reduction potentials, electroreduction mechanisms and acid-base chemistry was carried out on two series of free-base porphyrins in nonaqueous media. The first series is represented by four-pyrrole substituted tetraphenylporphyrin (TPP) derivatives, two of which are planar and two of which are nonplanar in their non-protonated form. The second comprises porphyrins with 0-4 meso-phenyl groups on the macrocycle. Equilibrium constants for conversion of each neutral porphyrin to its diprotic [H4P] 2+ form were determined and the electrochemistry was then elucidated as a function of: (i) type of nonaqueous solvent, (ii) anion of supporting electrolyte, …

free-base porphyrinsSupporting electrolyteprotonationInorganic chemistry010402 general chemistryElectrochemistry[ CHIM ] Chemical Sciences01 natural sciencesCatalysistetraphenylporphyrin monoacidschemistry.chemical_compoundconformational-analysismetal derivativesTetraphenylporphyrin[CHIM]Chemical SciencesReactivity (chemistry)tetraarylporphyrinsEquilibrium constantcomplexes010405 organic chemistryFree basecrystal-structurespectroelectrochemistryanionDiprotic acidPorphyrin0104 chemical sciencessupporting electrolytechemistryelectrochemistryexpanded porphyrindiacids[CHIM.OTHE]Chemical Sciences/Otherabsorption
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Demo 76. Decaimiento radiactivo: el "lacasitonio"

2013

Objetivo: Mostrar la naturaleza probabilística del decaimiento radiactivo mediante un juego interactivo que se basa en un sistema de dos estados. Introducir las magnitudes físicas que describen el decaimiento radiactivo. Verificar la ley de desintegración radiactiva de forma cuantitativa.

física cuántica estructura de la materia y estado sólidoconstante de desintegracióndecaimiento radiactivo
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Nonlinear nystagmus processing causes torsional VOR nonlinearity.

2003

The eye movement component that rotates around the line of sight, i.e., the ocular torsion, is in many aspects different from horizontal and vertical eye movements. While ocular torsion is mediated only by reflexive pathways like the torsional vestibulo-ocular and optokinetic reflexes (TVOR and OKN, respectively), horizontal and vertical components are also subject to intentional control mechanisms that are mediated by the saccadic and the pursuit systems. Dynamic properties of torsional eye movements are also very distinct. While horizontal and vertical VOR components show a gain close to unity and a small neural integration leakage with a time constant around pi=30 s, the TVOR shows a sma…

genetic structuresEye MovementsRotationModels NeurologicalNystagmusGeneral Biochemistry Genetics and Molecular BiologyOtolithic MembraneHistory and Philosophy of ScienceNystagmus PhysiologicControl theorymedicineHumansComputer SimulationPhysicsGeneral NeuroscienceTime constantTorsion (mechanics)Eye movementOptokinetic reflexReflex Vestibulo-Oculareye diseasesSaccadic maskingSemicircular CanalsNonlinear systemHead MovementsVestibulo–ocular reflexmedicine.symptomAnnals of the New York Academy of Sciences
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Complex-forming properties of peat humic acids from a raised bog profiles

2013

Abstract Humic substances (HS) belong to the most powerful complex-forming agents, significantly affecting major and trace element speciation in natural environment. Several authors have focused on humic–metal interactions, using differing methods and comparing humic substances on different sources. However, the intrinsic differences among the HS of different origin and the impact of humification degree on the complex formation between humic substances and metals have not received the necessary attention until now. The aim of this study is to determine the Cu(II) complexing capacity and stability constants of Cu(II) complexes of humic acids (HA) isolated from two well-characterized raised b…

geographyPeatgeography.geographical_feature_categoryMetal ions in aqueous solutionchemistry.chemical_elementcomplex mixturesCopperHumusIon selective electrodeMetalchemistryGeochemistry and PetrologyStability constants of complexesvisual_artEnvironmental chemistryvisual_art.visual_art_mediumEconomic GeologyBogJournal of Geochemical Exploration
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A synergic nanoantioxidant based on covalently modified halloysite–trolox nanotubes with intra-lumen loaded quercetin

2016

We describe the preparation and properties of the first example of a synergic nanoantioxidant, obtained by different functionalizations of the external surface and the inner lumen of halloysite nanotubes (HNTs). Trolox, a mimic of natural α-tocopherol, was selectively grafted on the HNT external surface; while quercetin, a natural polyphenolic antioxidant, was loaded into the inner lumen to afford a bi-functional nanoantioxidant, HNT–Trolox/Que, which was investigated for its reactivity with transient peroxyl radicals and a persistent 1,1-diphenyl-2-picrylhydrazyl (DPPH˙) radical in comparison with the corresponding mono-functional analogues HNT–Trolox and HNT/Que. Both HNT–Trolox and HNT/Q…

halloysite nanotubes antioxidants peroxyl radicals quercetin Trolox synergismAntioxidantRadicalmedicine.medical_treatmentBiomedical Engineering02 engineering and technology010402 general chemistry01 natural scienceschemistry.chemical_compoundReaction rate constantmedicinehalloysite trolox release quercetin antioxidantOrganic chemistryGeneral Materials ScienceAcetonitrileSettore CHIM/02 - Chimica FisicaAutoxidationChemistryGeneral ChemistryGeneral MedicineSettore CHIM/06 - Chimica Organica021001 nanoscience & nanotechnology0104 chemical sciencesChlorobenzeneTrolox0210 nano-technologyQuercetinNuclear chemistry
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Interplay of acidity and ionic liquid structure on the outcome of a heterocyclic rearrangement reaction

2021

The study of suitable probe reactions is a powerful tool to investigate the properties of nonconventional solvents such ionic liquids (ILs). In particular, we studied the acid-catalyzed mononuclear rearrangement of heterocycles (MHR) of the Z-phenylhydrazone of 5-amino-3-benzoyl-1,2,4-oxadiazole into the relevant 1,2,3-triazole, in solution of ILs by means of kinetic measurements. We chose as solvents six ILs differing both in the cation and anion, in the presence of five carboxylic and sulfonic acids as catalysts. For a useful comparison, the reaction was also performed in 1,4-dioxane and methanol. In general, the reaction occurs faster in ILs, compared to conventional solvents, according …

heterocyclic rearrangement010405 organic chemistryOrganic ChemistrySolvationacid catalysiSettore CHIM/06 - Chimica OrganicaIonic liquid010402 general chemistry01 natural sciencesMedicinal chemistryTransition state0104 chemical sciencesCatalysischemistry.chemical_compoundchemistryStability constants of complexesIonic liquidReactivity (chemistry)Rearrangement reactionMethanol
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