Diffractive vector meson production at HERA: From soft to hard QCD

Experimental results from HERA on diffractive vector meson production and their theoretical interpretation within microscopic QCD are reviewed with an emphasis on the BFKL color dipole and k _T -factorization approaches. The text was submitted by the authors in English.     

Generation of H− ions in a low-pressure xenon-hydrogen discharge. I

A theory of a low-pressure discharge in a xenon-molecular hydrogen mixture is developed. It is shown that, in such a discharge, at an interelectrode distance of L = 1 cm and a total plasma pressure of p ₀ ～ 1 Torr, the density of negative hydrogen ions produced via the dissociative attachment of thermal electrons to vibrationally excited molecules H₂ can reach a value as high as N_H ^? ≥ 10¹² cm^?3. According to calculations, the electron temperature in discharge operating regimes under study attains T _e ≈ 1?2 eV, which corresponds to the maximum of the e-v exchange rate constant of H₂ molecules. This ensures a relatively high rate of vibrational pumping of H₂ molecules in the discharge.     

Rational functions of best uniform approximation and holomorphic continuation of functions

Let f be a function, continuous and real valued on the segment Δ, Δ ⊂ (−∞, ∞) and {R_n} be the sequence of the rational functions of best uniform approximation to f on Δ of order (n, n). In the present work, the convergence of {R_n} in the complex plane is considered for the special caseswhen the poles (or the zeros, respectively) of {R_n} accumulate in the terms of weak convergence of measures to acompact set of zero capacity. As a consequence, sufficient conditions for the holomorphic and the meromorphic continuability of f are given. The work is supported by Project 69 with Ministry of Science and Education, Bulgaria.     

Geschwindigkeit der Verdünnung flüssiger Filme

Colloid and Polymer Science - Die Verdünnung eines mit löslichen Tensiden stabilisierten freien flüssigen Filmes wurde mit hydrodynamischen Methoden unter Berücksichtigung der...     

Topochemical investigations of peptide systems

The basic principles of the topochemical approach to the investigation of the structure-function relation in peptide systems are formulated. This approach makes use of the new possibility of transforming natural peptides, consisting in the modification of the molecule as a whole and utilization of the resultant analogs to elucidate the boundaries of the stereoelectronic complementarity of the biologically active peptide to the corresponding receptor. In particular, on the example of depsipeptide antibiotics and their topochemical analogs the fruitfulness of using such compounds as tools in elucidating the physicochemical basis of functioning of biological membranes is shown. The topochemical principle has also been applied in preparing specific competitive inhibitors of proteolytic enzymes, whose study may shed light on the nature of the forces binding the substrate to the contact site of the corresponding enzyme.     

Retention of analgin and anesthesin on sorbents with different polarities: The analysis of bellalgin tablets by high-performance liquid chromatography

The effects of acetonitrile and potassium dihydrogen phosphate concentrations in a mobile phase and the pH of the mobile phase on the retention of analgin (dipyrone) and anesthesin (benzocaine) on Symmetry C18 and Nova-Pak CN HP sorbents with grafted octadecylsilanol and nitrile groups, respectively, were studied. It was found that, under identical conditions, retention on the sorbent with grafted nitrile groups was weaker. A rapid and cost-effective procedure was developed for the determination of analgin and anesthesin in the analysis of Bellalgin tablets.     

Kinetic-chromatographic determination of 4-methylaminoantipyrine in Pentalgin N and Pentalgin FS tablets

4-Methylaminoantipyrine (4-MAAP) is the main product of analgin decomposition in aqueous-organic solutions used in the analysis of Pentalgin N and Pentalgin FS tablets. The determination of 4-MAAP in tablets is complicated by the fast decomposition of analgin in the course of sample dissolution. The use of nonaqueous solvents in subsequent HPLC analysis is unreasonable, because the shapes of analyte peaks are deteriorated and the decomposition of analgin is not prevented. A procedure for the kinetic-chromatographic determination of both 4-MAAP in tablets and its amount at the moment of sample dissolution is proposed.