Air-gap sulfide sensor with super-nernstian response in the low concentration range

An air-gap sulfide sensor is presented which operates on the basis of selective extraction of H₂S from an acidified sample into a small alkaline electrolyte film containing the dicyanoargentate (I) complex. This complex is partly decomposed during the measurement by the absorbed sulfide, and the potential of a silver sulfide-based indicator electrode which is in direct contact only with the electrolyte, then depends on the sulfide concentration of the sample. Because of the extraction and dissociation equilibria, the sensor responds in the low sulfide concentration range with a slope four times larger than that of a normal sulfide electrode. The lower limit of linearity is 10^?8 mol l^?1, because sulfide accumulates in the electrolyte film.     

Polymerisation cationique de l'indene amorcee par le tetrachlorure de titane-I Influence des impuretes du solvant,le chlorure de methylene,et effets cocatalytiques de l'eau et de l'acide chlorhydrique

The polymerization of the system indene-titanium tetrachloride-methylene chloride gave irreproducible kinetics which have been attributed to variable concentrations of impurities in the solvent. Incomplete yields sometimes observed at ?70° are also caused by impurities, but introduction of water and hydrochloric acid then gives complete yields. A new method of solvent purification has been used giving reproducible yields and rates. In such cases, monomer consumption at ?70° follows the rate law log [M]_o/[M] = kt.     

The influence of solute-solvent interactions on the kinetics and stereospecificity of polymerization-the relevance of aromatic solvent shifts observed on the nmr spectrum of methyl methacrylate

The effect of certain aromatic compounds on the PMR spectrum of methyl methacrylate (MMA) was investigated. The magnitude of observed aromatic-induced shifts decreased in the order benzene ? styrene > chlorobenzene ≈ bromobenzene.Assuming that the interaction arises from a stoichiometric 1:1 complex, equilibrium parameters for the MMA-benzene interaction have been estimated. ΔH ± S.E. (ΔH) = ?(8 ± 4) kJ mol^?1. These effects are likely to have a small influence on the kinetics of copolymerization with aromatic monomers and polymerization in aromatic solvent. The stereochemistry of the solute-solvent interactions suggests that MMA takes a cis-conformation in solution, which is relevant to the mechanism of stereoregular polymerizations of this monomer.     

Studies with model membranes

Summary Thermodynamic effective fixed charge densities of mercuric phosphate and carbonate parchment supported membranes were evaluated by a number of methods particularly those ofTeorell-Meyer-Sievers, Altug andHair andKobatake et al. The value of the permselectivity was obtained for the two membranes based onKobatake et al. procedure. Membrane transport number was calculated using a modified Nernst relation and compared with the values determined by the TMS method. The theoretical predictions for membrane potential usingKobatake et al. equation are borne out quite satisfactorily by our experimental results for both membrane.

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Zusammenfassung Es wurden die Dichte der fixierten Ladungen von Quecksilberphosphat und Quecksilberkarbonat-Niederschlagsmembranen nach den Methoden vonTorell-Meyer-Sievers, Altug undHair undKobatake bestimmt. Weiterhin wurden Durchlässigkeit und Transportzahlen ermittelt und mit Werten der TMS-Methode verglichen. Theoretische Voraussagen über das Membranpotential nach den Gleichungen vonKobatake stimmen mit den experimentellen Ergebnissen überein.

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With 8 figures and 3 tables     

Floating spherical gaussian orbital (FSGO) studies with a model potential: some open-shell systems

A gaussian based model potential is used within the FSGO formalism to study a series of open-shell systems (e.g. LiH⁺, NaH⁺, Li⁺₂ and LiNa⁺). Results for calculated equilibrium geometries and dissociation energies are compared to the corresponding quantities from available all-electron ab initio studies and other more elaborate theoretical estimates. The overall agreement is quite satisfactory.     

Mise au point d'un calorimetre de reaction en milieu fluorhydrique - enthalpies de dissolution de kf dans les solutions aqueuses de HF

A calorimeter designed for studies of reactions in hydrofluoric acid has been constructed. Enthalpies of dissolution of KF in aqueous solutions of HF (from 1,05 N to 28,3 N) have been measured.     

Kinetic Salt Effect in the 18O-Exchange Reaction between Bromate and Water

The kinetic salt effect in the ¹⁸O-exchange reaction between bromate ion and water has been investigated at 60° in a range of ionic strength from 0.02M < I < 1.9M using NaNO₃ or NaClO₄ as inert salts. From the experimental data the following relation was deduced for the uncatalysed reaction path In the H⁺-catalysed reaction path the Brønsted-Davies equation was obeyed up to I ? 0.1M At I > 0.8M the sign of Δ logk₂/Δ I^1/2 was positive. The theoretical interpretation of these results is consistent with the mechanistic evidence obtained previously from the rate law and the solvent isotope effects.     

The gas chromatography, thermal analysis and mass spectrometry of fluorinated lead β-diketonates Determination of traces of lead by the integrated ion-current technique

Preparative details for perfluoroalkanoylpivalylmethanes and their lead chelates are given. Thermal analysis, gas chromatography and mass spectral studies all indicate high thermal stability, but strong column interaction makes successful quantitative gas chromatography difficult. The integrated ion-current technique is applied to determine lead heptafluorobutanoylpivalylmethanate in the range 10^-9–10^-7 g of lead, but a lower detection limit of ca. 10^-14 g is indicated.     

Phototitrimetric determination of sulfhydryl compounds witho-hydroxymercuribenzoic acid using dithiofluorescein as an indicator

Summary A phototitrimetric method for the determination of sulfhydryl compounds in an aqueous medium is described.o-Hydroxymercuribenzoic acid is used as a titrant with dithiofluorescein as an indicator. Disulfide amino acids like cystine and-substituted DL-cystines are reduced with sodium borohydride before titration. All amino acids were determined to the limit of 1.0mol with an error of less than 4%. A selective phototitrimetric method for the determination of-mercaptopyruvate in presence of cysteine and glutathione is described. This method can be extended to the microdetermination of other similar sulfhydryl compounds in biological materials.

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Zusammenfassung Eine phototitrimetrische Bestimmungsmethode für Sulfhydrylverbindungen in wäßriger Phase wurde beschrieben. Als Maßflüssigkeit diento-Hydroxymercuribenzoesäure, als Indikator Dithiofluorescein. Aminosäuredisulfide wie Cystin und-substituierte DL-Cystine werden vor der Titration mit Natriumborhydrid reduziert. Alle Aminosäuren lassen sich bis zur Größenordnung von 1,0Mol mit einem Fehler von weniger als 4% bestimmen. Eine selektive phototitrimetrische Bestimmung von-Merkaptopyruvat in Gegenwart von Cystein und Glutathion wurde angegeben. Das Verfahren läßt sich auch für andere Sulfhydrylverbindungen in biologischem Material anwenden.