Direct titration of mercury (i) with potassium permanganate

Mercurous solutions can bc successfully titrated with potassium permanganate in presence of 0.5–1N H₂SO₄ and 1–1.5% NaF at 35–50°C, Sharp end-points arc obtained when the maximum concentration of monovalent mercury after mixing with the other reagents is 0.005N. At higher concentrations the reaction is sluggish and, the end-points arc not sharp.     

Synthesis of some novel S-alkylated and S-glycosylated hydantoin derivatives containing pyrene moiety

3-Aryl-5-[(Z)-pyrenylmethylene]-2-alkylthiohydantoins and 3-Aryl-5-[(Z)-pyrenylmethylene]-2-(D-glycosyl)-2-thiohydantoins functionalized with different aromatic and glycoside substituents have been synthesized by the reaction of (Z)-3-(4-methoxyphenyl)-5-[(pyren-8-yl)methylene]-2-thiohydantoin with alkyl halides, cyclic and acyclic nucleosides via various routes with moderate to good yields and characterized by ¹H, ¹³C NMR and mass spectra and elemental analysis     

Synthesis and characterization of new acyclic nucleosides analogues derived from 2-phenyl quinoline candidates

Reaction of 4-substituted quinoline hydrazide with some aldohexoses and aldopentoses gave a series of new N-β-glycosides. The following cyclization of N-β-glycosides with acetic anhydride led to O-acetyl-[5-(2-phenylquinolin-4-yl)-1,3,4-oxadiazol-2-yl]-D-glycosides. Structure of the newly synthesized products was elucidated by chemical and spectroscopic methods.     

Synergic extraction of trivalent gadolinium,europium and americium radionuclides by 15-crown-5 or 18-crown-6 mixed with thenoyltrifluoroacetone from perchlorate medium

Synergic extraction of trivalent Eu, Gd and Am from aqueous perchlorate medium has been studied using mixtures of thenoyltrifluoroacetone (HTTA) and 15-crown-5 or 18-crown-6 (CE) in chloroform at (25±1) °C. Slope analysis of the extraction results indicated a general formula of M(TTA)₃·(CE)₂ for the extracted species. The stability order took the sequence Eu(TTA)₃·(CE)₂>Am(TTA)₃)·(CE)_2>>Gd(TTA)₃·(CE)₂ with 15C5 and Am(TTA)₃·(CE)₂>Eu(TTA)₃·(CE)₂>Gd(TTA)₃·(CE)₂ with 18C6. The synergic factors, extracton constants and formation constants of the extracted species were determined and discussed in terms of the correspondence between cavity size of the crown ethers and ionic crystal radii.     

Tagungen

The extraction of uranium as well as Eu-(152 + 154), Co-60, Ru-103 and Cs-137 by di(2-ethylhexyl) phosphoric acid (HDEHP), tricaprylmethyl ammonium chloride (Aliquate-336) and tricapryltertiaryamine (Alamine-336) in kerosene from aqueous nitrate medium of constant ionic strength, 0.6 (H+, NaNO₃) was investigated. The aqueous phase used is a representative medium for certain medium level waste (MLW) solutions. The obtained results indicate that HDEHP system is more suitable for the separation of U(VI) and Eu(III) from Ru(III), Co(II) and Cs(I). Using HDEHP loaded on XAD-4, chromatographic extraction was applied successfully for the recovery of uranium and Eu(152+154) from the aforementioned solution.

Die Extraktion von Uranium wie auch von Eu-(152 + 154), Co-60, Ru-103 und Cs-137 durch Di(2-ethylhexyl) phosphorsäurc (HDEHP), Tricaprylmethylammoniumchlorid (Aliquate-336) und Tricapryl tertiäramin (Alamin-336) in Kerosin aus wäβrigen Nitratlösungen bei einer konstanten Ionenstärke von 0,6 (H+, NaNO₃) wurde untersucht. Die verwendete wäβrige Phase ist für eine mittelaktive Abfallösung (MLW) repräsentativ. Die Ergebnisse zeigen, daβ das HDEHP-System geeigneter zur Abtrennung des U(VI) und des Eu(III) vom Ru(III), Co(II) und Cs(I) ist. Bei Verwendung eines HDEHP-beladenen Austauschers (XAD-4) konnte eine chromatographische Extraktion zur Rückgewinnung des Uraniums und des Eu-(152 + 154) von der oben erwähnten Lösung erfolgreich angewendet werden.     

Synthesis and characterization of some novel substituted pyridones and iminopyridines derived from pyrene moiety

Russian Journal of General Chemistry - Two series with the general formula of 4,6-diaryl-2-oxo-1,2-dihydropyridine-3-carbonitriles and their isosteric...     

Approximation of the finite dimensional distributions of multiple fractional integrals

We construct a family Inεt(f) of continuous stochastic processes that converges in the sense of finite dimensional distributions to a multiple Wiener-Itô integral with respect to the fractional Brownian motion. We assume that and we prove our approximation result for the integrands f in a rather general class.     

Back titration with mercuric nitrate in alkaline medium

Summary The back titration procedure making use of mercuric nitrate as back titrant for excess EDTA in alkaline media, has been successfully applied for the determination of small amounts of scandium or palladium in the order of 0.045 to 7 or 0.1 to 4mg, respectively. Simple procedures are given for the analysis of binary or ternary mixtures of scandium or palladium with some other metals, yielding results of quite reasonable accuracy.

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Zusammenfassung Scandium oder Palladium können in Mengen von 0,045–7 bzw. 0,1–4 mg bestimmt werden, wenn man mit einem Überschuß an ÄDTA versetzt und in alkalischem Medium mit Quecksilber(II)-nitratlösung zurücktitriert. Auf einfache Weise können auch binäre und ternäre Gemische von Scandium oder Palladium mit anderen Metallen mit befriedigender Genauigkeit analysiert werden.

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See also: Z. analyt. Chemie 184, 92 (1961).     

Measurement of logarithmic decrements through the measurement of time

The paper describes an arrangement which can be used to measure the period and logarithmic decrement of a damped harmonic torsional oscillation without the need to perform any length measurements. By means of suitably arranged electronic circuits, all measurements are reduced to those of time intervals. These consist of a measurement of the period and of two time intervals which a travelling laser beam requires to sweep past two stationary photoresistances. A suitable procedure for the location of a zero base line is indicated, and it is shown that the residual uncertainty of this operation is the source of the dominant error.The paper contains an analysis of systematic and random errors of the method and mentions that decrements of the order of 0.05 can be measured with a relative error of the order of 0.06%.